diff options
| -rw-r--r-- | .gitattributes | 3 | ||||
| -rw-r--r-- | 78430-0.txt | 14306 | ||||
| -rw-r--r-- | 78430-h/78430-h.htm | 20037 | ||||
| -rwxr-xr-x | 78430-h/images/cover.jpg | bin | 0 -> 468977 bytes | |||
| -rw-r--r-- | 78430-h/images/fig_397.jpg | bin | 0 -> 6507 bytes | |||
| -rw-r--r-- | 78430-h/images/fig_398.jpg | bin | 0 -> 7647 bytes | |||
| -rw-r--r-- | 78430-h/images/fig_399.jpg | bin | 0 -> 6474 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_001colophon.jpg | bin | 0 -> 9568 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_010.jpg | bin | 0 -> 178915 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_012.jpg | bin | 0 -> 74596 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_012a.jpg | bin | 0 -> 13840 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_013.jpg | bin | 0 -> 11298 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_014.jpg | bin | 0 -> 64370 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_015.jpg | bin | 0 -> 49767 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_017.jpg | bin | 0 -> 42510 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_018.jpg | bin | 0 -> 146206 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_021.jpg | bin | 0 -> 40230 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_023.jpg | bin | 0 -> 35483 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_024.jpg | bin | 0 -> 25225 bytes | |||
| -rw-r--r-- | 78430-h/images/i_024a.jpg | bin | 0 -> 76065 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_026.jpg | bin | 0 -> 36393 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_027.jpg | bin | 0 -> 30318 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_027a.jpg | bin | 0 -> 10284 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_028.jpg | bin | 0 -> 28198 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_029.jpg | bin | 0 -> 19705 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_032.jpg | bin | 0 -> 26506 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_032a.jpg | bin | 0 -> 37568 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_033b.jpg | bin | 0 -> 34364 bytes | |||
| -rw-r--r-- | 78430-h/images/i_033xl.jpg | bin | 0 -> 31431 bytes | |||
| -rw-r--r-- | 78430-h/images/i_033xr.jpg | bin | 0 -> 36057 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_034.jpg | bin | 0 -> 50465 bytes | |||
| -rw-r--r-- | 78430-h/images/i_035_43.jpg | bin | 0 -> 45244 bytes | |||
| -rw-r--r-- | 78430-h/images/i_035_44.jpg | bin | 0 -> 40107 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_036.jpg | bin | 0 -> 59800 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_040.jpg | bin | 0 -> 29232 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_045.jpg | bin | 0 -> 62280 bytes | |||
| -rw-r--r-- | 78430-h/images/i_046x.jpg | bin | 0 -> 15584 bytes | |||
| -rw-r--r-- | 78430-h/images/i_047.jpg | bin | 0 -> 77938 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_047x.jpg | bin | 0 -> 58976 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_051.jpg | bin | 0 -> 33411 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_052.jpg | bin | 0 -> 14510 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_052a.jpg | bin | 0 -> 13912 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_053.jpg | bin | 0 -> 43258 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_054.jpg | bin | 0 -> 55425 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_055.jpg | bin | 0 -> 16971 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_057.jpg | bin | 0 -> 27059 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_058.jpg | bin | 0 -> 32053 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_058x.jpg | bin | 0 -> 33570 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_059.jpg | bin | 0 -> 15835 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_061.jpg | bin | 0 -> 32342 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_063.jpg | bin | 0 -> 16502 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_066.jpg | bin | 0 -> 57352 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_067.jpg | bin | 0 -> 71347 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_069.jpg | bin | 0 -> 35641 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_070.jpg | bin | 0 -> 42060 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_071.jpg | bin | 0 -> 26962 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_072.jpg | bin | 0 -> 8625 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_072a.jpg | bin | 0 -> 40522 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_073.jpg | bin | 0 -> 65625 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_074.jpg | bin | 0 -> 57268 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_077.jpg | bin | 0 -> 18418 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_078.jpg | bin | 0 -> 63806 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_079.jpg | bin | 0 -> 61155 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_079a.jpg | bin | 0 -> 107547 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_080.jpg | bin | 0 -> 50373 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_083.jpg | bin | 0 -> 138988 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_084.jpg | bin | 0 -> 29575 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_084a.jpg | bin | 0 -> 31396 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_086.jpg | bin | 0 -> 18115 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_086a.jpg | bin | 0 -> 52019 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_087.jpg | bin | 0 -> 29910 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_088.jpg | bin | 0 -> 51723 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_092.jpg | bin | 0 -> 48219 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_093.jpg | bin | 0 -> 46451 bytes | |||
| -rw-r--r-- | 78430-h/images/i_094.jpg | bin | 0 -> 8329 bytes | |||
| -rw-r--r-- | 78430-h/images/i_094_94.jpg | bin | 0 -> 30601 bytes | |||
| -rw-r--r-- | 78430-h/images/i_094_95.jpg | bin | 0 -> 59802 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_095.jpg | bin | 0 -> 20689 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_096.jpg | bin | 0 -> 21108 bytes | |||
| -rw-r--r-- | 78430-h/images/i_096a.jpg | bin | 0 -> 33580 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_097.jpg | bin | 0 -> 51345 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_099.jpg | bin | 0 -> 20983 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_100.jpg | bin | 0 -> 13793 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_100a.jpg | bin | 0 -> 34751 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_101.jpg | bin | 0 -> 28044 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_101a.jpg | bin | 0 -> 13683 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_102.jpg | bin | 0 -> 71588 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_102x.jpg | bin | 0 -> 101452 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_103x.jpg | bin | 0 -> 20073 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_104.jpg | bin | 0 -> 6651 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_106.jpg | bin | 0 -> 14163 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_107.jpg | bin | 0 -> 5950 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_108.jpg | bin | 0 -> 12152 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_109.jpg | bin | 0 -> 165859 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_110.jpg | bin | 0 -> 88713 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_110a.jpg | bin | 0 -> 84135 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_111.jpg | bin | 0 -> 27221 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_112.jpg | bin | 0 -> 41264 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_113.jpg | bin | 0 -> 119625 bytes | |||
| -rw-r--r-- | 78430-h/images/i_114.jpg | bin | 0 -> 242012 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_116.jpg | bin | 0 -> 67741 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_116a.jpg | bin | 0 -> 28946 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_117.jpg | bin | 0 -> 16006 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_118.jpg | bin | 0 -> 143897 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_120.jpg | bin | 0 -> 53375 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_121.jpg | bin | 0 -> 10692 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_123.jpg | bin | 0 -> 32370 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_123a.jpg | bin | 0 -> 9086 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_124.jpg | bin | 0 -> 41706 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_125.jpg | bin | 0 -> 15350 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_127.jpg | bin | 0 -> 85227 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_129.jpg | bin | 0 -> 81315 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_129a.jpg | bin | 0 -> 54756 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_130.jpg | bin | 0 -> 17533 bytes | |||
| -rw-r--r-- | 78430-h/images/i_130a.jpg | bin | 0 -> 18067 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_131.jpg | bin | 0 -> 34121 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_131a.jpg | bin | 0 -> 28980 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_132.jpg | bin | 0 -> 115548 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_132a.jpg | bin | 0 -> 94321 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_133.jpg | bin | 0 -> 11146 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_133a.jpg | bin | 0 -> 47814 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_135.jpg | bin | 0 -> 155918 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_136.jpg | bin | 0 -> 18260 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_136a.jpg | bin | 0 -> 21098 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_140.jpg | bin | 0 -> 50266 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_141.jpg | bin | 0 -> 28634 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_141a.jpg | bin | 0 -> 25583 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_142.jpg | bin | 0 -> 9547 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_143.jpg | bin | 0 -> 12020 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_143a.jpg | bin | 0 -> 49465 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_144.jpg | bin | 0 -> 12333 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_145.jpg | bin | 0 -> 25794 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_145a.jpg | bin | 0 -> 7674 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_146.jpg | bin | 0 -> 7133 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_147.jpg | bin | 0 -> 34637 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_147a.jpg | bin | 0 -> 7304 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_148.jpg | bin | 0 -> 11209 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_149.jpg | bin | 0 -> 29764 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_149a.jpg | bin | 0 -> 8358 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_149b.jpg | bin | 0 -> 22451 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_149c.jpg | bin | 0 -> 30880 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_150.jpg | bin | 0 -> 22184 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_151.jpg | bin | 0 -> 67675 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_151a.jpg | bin | 0 -> 17100 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_152.jpg | bin | 0 -> 55394 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_152a.jpg | bin | 0 -> 21639 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_153.jpg | bin | 0 -> 7549 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_153a.jpg | bin | 0 -> 28014 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_153b.jpg | bin | 0 -> 28680 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_153c.jpg | bin | 0 -> 51754 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_154.jpg | bin | 0 -> 31241 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_154a.jpg | bin | 0 -> 21238 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_157.jpg | bin | 0 -> 14409 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_157a.jpg | bin | 0 -> 7433 bytes | |||
| -rw-r--r-- | 78430-h/images/i_158a.jpg | bin | 0 -> 22302 bytes | |||
| -rw-r--r-- | 78430-h/images/i_158b.jpg | bin | 0 -> 42337 bytes | |||
| -rw-r--r-- | 78430-h/images/i_158c.jpg | bin | 0 -> 14846 bytes | |||
| -rw-r--r-- | 78430-h/images/i_159.jpg | bin | 0 -> 121460 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_160.jpg | bin | 0 -> 16892 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_160a.jpg | bin | 0 -> 75585 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_161.jpg | bin | 0 -> 168581 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_162.jpg | bin | 0 -> 21257 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_162a.jpg | bin | 0 -> 28161 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_163.jpg | bin | 0 -> 29433 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_163a.jpg | bin | 0 -> 32289 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_165.jpg | bin | 0 -> 36982 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_165a.jpg | bin | 0 -> 21870 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_165b.jpg | bin | 0 -> 31114 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_166.jpg | bin | 0 -> 54965 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_166a.jpg | bin | 0 -> 31651 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_210.jpg | bin | 0 -> 12878 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_211.jpg | bin | 0 -> 10364 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_212.jpg | bin | 0 -> 30010 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_213.jpg | bin | 0 -> 16911 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_214.jpg | bin | 0 -> 22531 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_215.jpg | bin | 0 -> 12755 bytes | |||
| -rw-r--r-- | 78430-h/images/i_168_216.jpg | bin | 0 -> 11628 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_172.jpg | bin | 0 -> 146027 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_174.jpg | bin | 0 -> 18388 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_175.jpg | bin | 0 -> 25452 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_175a.jpg | bin | 0 -> 50692 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_176.jpg | bin | 0 -> 48665 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_177.jpg | bin | 0 -> 134257 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_177a.jpg | bin | 0 -> 11371 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_179.jpg | bin | 0 -> 17415 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_179a.jpg | bin | 0 -> 35130 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_180.jpg | bin | 0 -> 35538 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_185.jpg | bin | 0 -> 18748 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_187.jpg | bin | 0 -> 24462 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_188.jpg | bin | 0 -> 18444 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_189.jpg | bin | 0 -> 234610 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_190.jpg | bin | 0 -> 37142 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_190a.jpg | bin | 0 -> 38916 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_191.jpg | bin | 0 -> 116295 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_191a.jpg | bin | 0 -> 18224 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_191b.jpg | bin | 0 -> 30104 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_192.jpg | bin | 0 -> 68731 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_193.jpg | bin | 0 -> 68524 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_193a.jpg | bin | 0 -> 46935 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_195.jpg | bin | 0 -> 13173 bytes | |||
| -rw-r--r-- | 78430-h/images/i_195_252.jpg | bin | 0 -> 14335 bytes | |||
| -rw-r--r-- | 78430-h/images/i_195_253.jpg | bin | 0 -> 17703 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_196.jpg | bin | 0 -> 119020 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_200.jpg | bin | 0 -> 114389 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_200a.jpg | bin | 0 -> 62744 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_201.jpg | bin | 0 -> 147564 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_202.jpg | bin | 0 -> 52743 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_202a.jpg | bin | 0 -> 70943 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_203.jpg | bin | 0 -> 130710 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_207.jpg | bin | 0 -> 49638 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_207a.jpg | bin | 0 -> 36321 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_208.jpg | bin | 0 -> 40786 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_209.jpg | bin | 0 -> 35349 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_210.jpg | bin | 0 -> 29797 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_211.jpg | bin | 0 -> 31057 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_211a.jpg | bin | 0 -> 21536 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_213.jpg | bin | 0 -> 59584 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_214.jpg | bin | 0 -> 55014 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_215.jpg | bin | 0 -> 67297 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_215a.jpg | bin | 0 -> 32331 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_215b.jpg | bin | 0 -> 23953 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_215c.jpg | bin | 0 -> 32021 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_216.jpg | bin | 0 -> 19679 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_217.jpg | bin | 0 -> 45401 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_218.jpg | bin | 0 -> 102818 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_219.jpg | bin | 0 -> 17705 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_219a.jpg | bin | 0 -> 51598 bytes | |||
| -rw-r--r-- | 78430-h/images/i_220.jpg | bin | 0 -> 37027 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_222.jpg | bin | 0 -> 43013 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_223.jpg | bin | 0 -> 71254 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_225.jpg | bin | 0 -> 53308 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_227.jpg | bin | 0 -> 85789 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_227a.jpg | bin | 0 -> 37526 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_228.jpg | bin | 0 -> 42480 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_228a.jpg | bin | 0 -> 38312 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_231.jpg | bin | 0 -> 12564 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_232.jpg | bin | 0 -> 100133 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_234.jpg | bin | 0 -> 41041 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_234a.jpg | bin | 0 -> 45793 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_235.jpg | bin | 0 -> 150574 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_237.jpg | bin | 0 -> 170136 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_238.jpg | bin | 0 -> 62361 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_238a.jpg | bin | 0 -> 40324 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_241.jpg | bin | 0 -> 145425 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_242.jpg | bin | 0 -> 87798 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_243.jpg | bin | 0 -> 60956 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_246.jpg | bin | 0 -> 23256 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_246a.jpg | bin | 0 -> 40212 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_247.jpg | bin | 0 -> 36032 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_247a.jpg | bin | 0 -> 31001 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_248.jpg | bin | 0 -> 32195 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_250.jpg | bin | 0 -> 89518 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_253.jpg | bin | 0 -> 18442 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_253a.jpg | bin | 0 -> 18058 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_253b.jpg | bin | 0 -> 38397 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_254.jpg | bin | 0 -> 62625 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_254a.jpg | bin | 0 -> 18282 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_255.jpg | bin | 0 -> 45166 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_256.jpg | bin | 0 -> 66549 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_256a.jpg | bin | 0 -> 68777 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_257.jpg | bin | 0 -> 32076 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_257a.jpg | bin | 0 -> 9123 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_261.jpg | bin | 0 -> 185986 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_263.jpg | bin | 0 -> 48576 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_265.jpg | bin | 0 -> 43128 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_266.jpg | bin | 0 -> 19172 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_266a.jpg | bin | 0 -> 20102 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_267.jpg | bin | 0 -> 33695 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_268.jpg | bin | 0 -> 13058 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_268a.jpg | bin | 0 -> 26845 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_269.jpg | bin | 0 -> 17520 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_271.jpg | bin | 0 -> 29306 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_271a.jpg | bin | 0 -> 29101 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_271b.jpg | bin | 0 -> 26691 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_272.jpg | bin | 0 -> 28860 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_272a.jpg | bin | 0 -> 27714 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_272b.jpg | bin | 0 -> 11975 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_273.jpg | bin | 0 -> 20173 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_273a.jpg | bin | 0 -> 24714 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_273b.jpg | bin | 0 -> 31094 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_274.jpg | bin | 0 -> 11885 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_274a.jpg | bin | 0 -> 37557 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_276.jpg | bin | 0 -> 69355 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_277.jpg | bin | 0 -> 88014 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_278.jpg | bin | 0 -> 59428 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_278a.jpg | bin | 0 -> 49987 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_282.jpg | bin | 0 -> 160701 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_284.jpg | bin | 0 -> 186477 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_285.jpg | bin | 0 -> 73789 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_285a.jpg | bin | 0 -> 20303 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_286.jpg | bin | 0 -> 27890 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_288.jpg | bin | 0 -> 193390 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_289.jpg | bin | 0 -> 24831 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_290.jpg | bin | 0 -> 22684 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_290a.jpg | bin | 0 -> 85080 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_291.jpg | bin | 0 -> 196468 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_292.jpg | bin | 0 -> 161761 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_294.jpg | bin | 0 -> 230865 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_295.jpg | bin | 0 -> 238526 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_298.jpg | bin | 0 -> 74228 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_300.jpg | bin | 0 -> 83256 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_300a.jpg | bin | 0 -> 72469 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_303.jpg | bin | 0 -> 215565 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_307.jpg | bin | 0 -> 37682 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_307a.jpg | bin | 0 -> 31221 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_308.jpg | bin | 0 -> 20841 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_308a.jpg | bin | 0 -> 26064 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_310.jpg | bin | 0 -> 24403 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_312.jpg | bin | 0 -> 36739 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_313.jpg | bin | 0 -> 74680 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_314.jpg | bin | 0 -> 156296 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_315.jpg | bin | 0 -> 36041 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_318.jpg | bin | 0 -> 59638 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_319.jpg | bin | 0 -> 57736 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_321.jpg | bin | 0 -> 43100 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_325.jpg | bin | 0 -> 63107 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_327.jpg | bin | 0 -> 40982 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_328.jpg | bin | 0 -> 33098 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_328a.jpg | bin | 0 -> 97101 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_329.jpg | bin | 0 -> 11160 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_330.jpg | bin | 0 -> 129857 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_331.jpg | bin | 0 -> 109474 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_334.jpg | bin | 0 -> 44892 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_334a.jpg | bin | 0 -> 54697 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_335.jpg | bin | 0 -> 18831 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_335a.jpg | bin | 0 -> 29758 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_336.jpg | bin | 0 -> 64858 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_336a.jpg | bin | 0 -> 30261 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_337.jpg | bin | 0 -> 48692 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_337a.jpg | bin | 0 -> 29647 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_338.jpg | bin | 0 -> 88063 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_339.jpg | bin | 0 -> 37264 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_340.jpg | bin | 0 -> 62786 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_341.jpg | bin | 0 -> 136350 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_342.jpg | bin | 0 -> 69766 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_343.jpg | bin | 0 -> 104469 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_345.jpg | bin | 0 -> 130292 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_346.jpg | bin | 0 -> 14777 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_347.jpg | bin | 0 -> 45700 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_347a.jpg | bin | 0 -> 35782 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_348.jpg | bin | 0 -> 55485 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_351.jpg | bin | 0 -> 64607 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_352.jpg | bin | 0 -> 29610 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_353.jpg | bin | 0 -> 29626 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_353a.jpg | bin | 0 -> 28232 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_355.jpg | bin | 0 -> 163124 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_357.jpg | bin | 0 -> 80556 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_357a.jpg | bin | 0 -> 33272 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_358.jpg | bin | 0 -> 29076 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_358a.jpg | bin | 0 -> 40935 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_359.jpg | bin | 0 -> 43834 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_360.jpg | bin | 0 -> 40261 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_361.jpg | bin | 0 -> 87292 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_363.jpg | bin | 0 -> 13318 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_366.jpg | bin | 0 -> 76469 bytes | |||
| -rwxr-xr-x | 78430-h/images/i_371.jpg | bin | 0 -> 45987 bytes | |||
| -rw-r--r-- | 78430-h/images/i_378.jpg | bin | 0 -> 30624 bytes | |||
| -rw-r--r-- | LICENSE.txt | 11 | ||||
| -rw-r--r-- | README.md | 2 |
359 files changed, 34359 insertions, 0 deletions
diff --git a/.gitattributes b/.gitattributes new file mode 100644 index 0000000..6833f05 --- /dev/null +++ b/.gitattributes @@ -0,0 +1,3 @@ +* text=auto +*.txt text +*.md text diff --git a/78430-0.txt b/78430-0.txt new file mode 100644 index 0000000..0a01457 --- /dev/null +++ b/78430-0.txt @@ -0,0 +1,14306 @@ +*** START OF THE PROJECT GUTENBERG EBOOK 78430 *** + + + + + TRANSCRIBER’S NOTE + + - Some minor changes to the text are noted at the end of the book. + - Italic text is denoted by _underscores_. + - Bold text is denoted by =equal signs=. + - Small-cap text has been changed to ALL-CAP text. + - Footnote anchors are denoted by [number], and the footnotes have + been placed at the end of the book. + + + + + A PRACTICAL COURSE IN + BOTANY + + WITH ESPECIAL REFERENCE TO ITS BEARINGS ON + + AGRICULTURE, ECONOMICS, AND SANITATION + + + BY + + E. F. ANDREWS + AUTHOR OF “BOTANY ALL THE YEAR ROUND” + + + WITH EDITORIAL REVISION BY + + FRANCIS E. LLOYD + + MACDONALD PROFESSOR OF BOTANY, McGILL UNIVERSITY, + FORMERLY OF ALABAMA POLYTECHNIC INSTITUTE + + [Illustration] + + + NEW YORK ·:· CINCINNATI ·:· CHICAGO + AMERICAN BOOK COMPANY + + + + + COPYRIGHT, 1911, BY + E. F. ANDREWS. + + ENTERED AT STATIONERS’ HALL, LONDON. + + + ANDREW’S PR. BOTANY. + + W. P. 7 + + + + +PREFACE + + +In preparing the present volume, the aim of the writer has been to +meet all the college entrance requirements and at the same time +to bring the study of botany into closer touch with the practical +business of life by stressing its relations with agriculture, +economics, and, in certain of its aspects, with sanitation. While +technical language has been avoided so far as the requirements of +scientific accuracy will permit, the student is not encouraged +to shirk the use of necessary botanical terms, out of a mere +superstitious fear of words because they happen to be a little new or +unfamiliar. Such a practice not only leads to careless and inaccurate +modes of expression, but tends to foster a slovenly habit of mind, +and in the long run causes the waste of more time and labor in the +search after roundabout, and often misleading, substitutes, than it +would require to master the proper use of a few new words and phrases. + +In the choice of materials for experiment and illustration, the +endeavor has been to call for such only as are familiar and easily +obtained. The specimens for flower dissection have been selected +mainly from common cultivated kinds, because their wide distribution +makes them easy to obtain everywhere, while in cities and large +towns they are practically the only specimens available. Another +important consideration has been the desire to spare our native +wild flowers, or at least not to hasten the extinction with which +they are threatened by the ravages of Sunday excursionists and +summer tourists, to whose unthinking, but none the less destructive, +incursions, the automobile has laid open the most secret haunts +of nature. The influence of the public school teacher, and more +especially the teacher of botany, is the most potent factor from +which we can hope for aid in putting a stop to the relentless +persecution that has practically exterminated many of our choicest +wild plants and is fast reducing the civilized world to a depressing +monotony of weediness and artificiality. Except for purely systematic +and anatomical work, flowers can be studied to better purpose in +their living, active state than as dead subjects for dissection; +and the best way to show our interest in them, or to get the most +rational enjoyment out of them, is not, as a general thing, to +cut their heads off and throw them away to wither and die by the +roadside. The teacher, by instilling into the minds of the rising +generation a reverence for plant life, may do a great deal to aid +in the conservation of one of our chief national assets for the +gratification of the higher esthetic instincts. The fruits and +flowers of cultivation do not stand in the same need of protection, +since they are produced solely with a view to the use and pleasure of +man, and their propagation is provided for to meet all his demands. + +To avoid too frequent interruptions of the subject matter, the +experiments are grouped together at the beginning or end of the +sections to which they belong, according as they are intended to +explain what is coming, or to illustrate what has gone before. A few +exceptions are made in cases where the experiment is such an integral +part of the subject that it would be meaningless if separated from +the context. Under no circumstances should those capable of being +performed in the schoolroom be omitted, as much of the information +which the book is intended to give is conveyed by their means. For +this reason, and also because the aim of the book is to present the +science from a practical rather than from an academic point of view, +the experiments outlined are for the most part of a simple, practical +nature, such as can be performed by the pupils themselves with a +moderate expenditure of ingenuity and money. The experience of the +writer has been that for the average boy or girl who wishes to get +a good general knowledge of the subject, but does not propose to +become a specialist in botany, the best results are often obtained +by the use of the simplest and most familiar appliances, as in +this way attention is not distracted from the experiment itself to +the unfamiliar apparatus for making it. In saying this, it is not +meant to underrate the value of a complete laboratory equipment, +but merely to emphasize the fact that the lack of it, while a +disadvantage, need not be an insuperable bar to the successful +teaching of botany. It is, of course, taken for granted that in +schools provided with a suitable laboratory outfit, teachers will be +prepared to supplement or to replace the exercises here outlined with +such others as in their judgment the subject may demand. There are as +many ideals in teaching as there are teachers, and the most that a +textbook can do is to present a working model which every teacher is +free to modify in accordance with his or her own method. + +The writer takes pleasure in acknowledging here the many obligations +due to Professor Francis E. Lloyd, of the Botanical Department of the +Alabama Polytechnic Institute, at Auburn, Ala., for his valuable aid +in the revision of the manuscript, for the highly interesting series +of illustrations relating to phototropic movements, and for advice +and information on points demanding expert knowledge which have +contributed very materially to whatever merit this volume may possess. + +Other members of the Auburn faculty to whom the author feels +especially indebted are Mr. C. S. Ridgeway, assistant in the +Botanical Department, Professor J. E. Duggar, of the Agricultural +Department, and Dr. B. B. Ross and Professor C. W. Williamson of the +Department of Chemistry. Acknowledgments are due also to Professor +George Wood of the Boys’ High School, Brooklyn, for suggestions +which have been of great assistance in the preparation of this work; +to Professor W. R. Dodson, of the University of Louisiana, for +illustrative material furnished, and to Professor William Trelease +for the loan of original material used in reproducing the beautiful +cuts from the Reports of the Missouri Botanical Garden, credit for +which is given in the proper place. + +For original photographs and drawings by the author, and familiar +selections from well-known works, which can be generally recognized, +it has not been thought necessary to give special credit. + + E. F. ANDREWS. + + AUBURN, ALABAMA. + + + + + FULL-PAGE ILLUSTRATIONS + + + PLATE PAGE + + 1. A GROVE OF LIVE OAKS NEAR SAVANNAH, GEORGIA _Frontispiece_ + + 2. CARRYING WATER OVER THE MISSISSIPPI LEVEE BY SIPHON TO + IRRIGATE RICE FIELDS 8 + + 3. AËRIAL ROOTS OF A MEXICAN STRANGLING FIG 73 + + 4. A FOREST OF BAMBOO 99 + + 5. A GROUP OF CONIFERS 108 + + 6. A WHITE OAK, SHOWING THE GREAT SPREAD OF BRANCHES 117 + + 7. A TIMBER TREE SPOILED BY STANDING TOO MUCH ALONE 125 + + 8. AN AMERICAN ELM, ILLUSTRATING DELIQUESCENT GROWTH 130 + + 9. VEGETATION OF A MOIST, SHADY RAVINE 151 + + 10. A MOSAIC OF MOONSEED LEAVES 179 + + 11. HYBRID BETWEEN A RED AND A WHITE CARNATION 227 + + 12. GOOSEBERRIES, SHOWING IMPROVEMENT BY SELECTION 251 + + 13. THE EFFECTS OF IRRIGATION 272 + + 14. A XEROPHYTE FORMATION OF YUCCAS AND SWITCH PLANTS 282 + + 15. A GIANT TULIP TREE OF THE SOUTH ATLANTIC FOREST REGION 293 + + + + + CONTENTS + + + CHAPTER I. THE SEED PAGE + + I. THE STORAGE OF FOOD IN SEEDS 1 + + II. SOME PHYSIOLOGICAL PROPERTIES OF SEEDS 10 + + III. TYPES OF SEEDS 12 + + IV. SEED DISPERSAL 21 + + FIELD WORK 28 + + + CHAPTER II. GERMINATION AND GROWTH + + I. PROCESSES ACCOMPANYING GERMINATION 29 + + II. CONDITIONS OF GERMINATION 33 + + III. DEVELOPMENT OF THE SEEDLING 40 + + IV. GROWTH 47 + + FIELD WORK 52 + + + CHAPTER III. THE ROOT + + I. OSMOSIS AND THE ACTION OF THE CELL 53 + + II. MINERAL NUTRIMENTS ABSORBED BY PLANTS 58 + + III. STRUCTURE OF THE ROOT 61 + + IV. THE WORK OF ROOTS 65 + + V. DIFFERENT FORMS OF ROOTS 72 + + FIELD WORK 80 + + + CHAPTER IV. THE STEM + + I. FORMS AND GROWTH OF STEMS 81 + + II. MODIFICATIONS OF THE STEM 88 + + III. STEM STRUCTURE + + A. MONOCOTYLS 96 + + B. HERBACEOUS DICOTYLS 102 + + C. WOODY STEMMED DICOTYLS 107 + + IV. THE WORK OF STEMS 112 + + V. WOOD STRUCTURE IN ITS RELATION TO INDUSTRIAL USES 118 + + VI. FORESTRY 124 + + FIELD WORK 128 + + + CHAPTER V. BUDS AND BRANCHES + + I. MODES OF BRANCHING 131 + + II. BUDS 138 + + III. THE BRANCHING OF FLOWER STEMS 141 + + FIELD WORK 145 + + + CHAPTER VI. THE LEAF + + I. THE TYPICAL LEAF AND ITS PARTS 147 + + II. THE VEINING AND LOBING OF LEAVES 154 + + III. TRANSPIRATION 160 + + IV. ANATOMY OF THE LEAF 164 + + V. FOOD MAKING 168 + + VI. THE LEAF AN ORGAN OF RESPIRATION 174 + + VII. THE ADJUSTMENT OF LEAVES TO EXTERNAL RELATIONS 177 + + VIII. MODIFIED LEAVES 189 + + FIELD WORK 194 + + + CHAPTER VII. THE FLOWER + + I. DISSECTION OF TYPES WITH SUPERIOR OVARY 196 + + II. DISSECTION OF TYPES WITH INFERIOR OVARY 204 + + III. STUDY OF A COMPOSITE FLOWER 210 + + IV. SPECIALIZED FLOWERS 214 + + V. FUNCTION AND WORK OF THE FLOWER 219 + + VI. HYBRIDIZATION 223 + + VII. PLANT BREEDING 230 + + VIII. ECOLOGY OF THE FLOWER + + A. THE PREVENTION OF SELF-POLLINATION 235 + + B. WIND POLLINATION 239 + + C. INSECT POLLINATION 241 + + D. PROTECTIVE ADAPTATION 245 + + FIELD WORK 249 + + + CHAPTER VIII. FRUITS + + I. HORTICULTURAL AND BOTANICAL FRUITS 250 + + II. FLESHY FRUITS 255 + + III. DRY FRUITS 260 + + IV. ACCESSORY, AGGREGATE, AND MULTIPLE FRUITS 265 + + FIELD WORK 269 + + + CHAPTER IX. THE RESPONSE OF THE PLANT TO + ITS SURROUNDINGS + + I. ECOLOGICAL FACTORS 271 + + II. PLANT ASSOCIATIONS 277 + + III. ZONES OF VEGETATION 288 + + FIELD WORK 294 + + + CHAPTER X. CRYPTOGAMS + + I. THEIR PLACE IN NATURE 296 + + II. ALGÆ 299 + + III. FUNGI 303 + + A. BACTERIA 306 + + B. YEASTS 314 + + C. RUSTS 317 + + D. MUSHROOMS 323 + + IV. LICHENS 329 + + V. LIVERWORTS 334 + + VI. MOSSES 341 + + VII. FERN PLANTS 344 + + VIII. THE RELATION BETWEEN CRYPTOGAMS AND SEED PLANTS 354 + + IX. THE COURSE OF PLANT EVOLUTION 359 + + FIELD WORK 362 + + + APPENDIX + + 1. SYSTEMATIC BOTANY 364 + + 2. WEIGHTS, MEASURES, AND TEMPERATURES 367 + + +[Illustration: PLATE 1.—Live oaks covered with Spanish moss +(_Tillandsia_).] + + + + +CHAPTER I. THE SEED + + + I. THE STORAGE OF FOOD IN SEEDS + + MATERIAL.—In addition to the four food tests described in Exps. + 1-6, there should be provided some raw starch, a solution of grape + sugar, the white of a hard-boiled egg, and any fatty substance, + such as lard or oil. For Exps. 8 and 9, a little diastase solution + will be necessary. “Taka” diastase, made from rice acted upon by a + fungus, can be obtained for a trifle at almost any drug store. + + LIVING MATERIAL.—Grains of corn and wheat, and seeds of some kind + of bean, the larger the better. The “horse bean” (_Vicia faba_), + if it can be obtained, makes an excellent object for study, as the + cells are so large that they can be seen with the naked eye. For + showing the presence of proteins (aleurone grains) and oily matter, + use thin cross sections through the kernel of a castor bean or a + Brazil nut. Specimens for the study of the individual cell will be + found in the hairs growing on squash seedlings, in the epidermis of + one of the inner coats of an onion, in the roots of oat or radish + seedlings, or in the section of a young corn root. + + A compound microscope will be required for this study. + +=1. The economic importance of seeds.=—As a source of food to both +man and the lower animals, the importance of seeds can hardly be +overrated. All the flour, meal, rice, hominy, and other breadstuffs +sold in the market come from them, to say nothing of the fleece from +the cotton seed that clothes the greater part of the world, besides +furnishing a substitute for lard and an important food for cattle. +The oils and fats stored in nuts are also to be taken into account, +the peanut alone yielding the greater part of the so-called olive +oil of commerce. Since the value of our farm crops depends largely +upon the kind and quantity of these substances furnished by them, it +is worth our while, as a matter of economic as well as scientific +interest, to learn something about the nature of the different foods +contained in plants. + +[Illustration: FIGS. 1-3.—The world’s three most important food +grains (magnified): 1, section of a rice grain; _a_, cuticle; _b_, +aleurone, or protein layer; _c_, starch cells; _d_, germ; 2, section +of a wheat grain; _k_, germ; _s_, starch; _a_, gluten; _t_, _t_, +_t_, layers of the seed coat; 3, section of a grain of corn; _c_, +husk; _e_, aleurone layer containing proteins; _eg_, yellowish, +horny endosperm, containing proteins and starch; _ew_, lighter +starchy endosperm: the darker part below is rich in oil and proteins, +and contains the _embryo_, consisting of the absorbing organ, or +_cotyledon_, _sc_; the rudimentary bud, _s_; and the root, _w_. (1, +from Circular 77, La. Exp. Station; 2, from Francé; 3, from Sachs.)] + +=2. Why food is stored in seeds.=—The one purpose for which plants +produce their seed is to give rise to a new generation and so carry +on the life of the species. The seed is the nursery, so to speak, in +which the germ destined to produce a new plant is sheltered until +it is ready to begin an independent existence. But the young plant, +like the young animal, is incapable of providing for itself at first, +and would die unless it received nourishment from the mother plant +until it has formed roots and leaves so that it can manufacture food +for itself. Plants in general require very much the same food that +animals do, and they have the power, which animals have not, of +manufacturing it out of the crude materials contained in the soil +water and in the air. Such of these foods as are not needed for +immediate consumption, they store up to serve as a provision for the +young shoot when the seed begins to germinate. + +[Illustration: FIGS. 4-7.—Sections of corn grains showing different +qualities of food contents: 4, 5, small germ and large proportion +of horny part, showing high protein; 6, 7, large germ and smaller +proportion of horny part, showing high oil content.] + +=3. Food substances contained in seeds.=—There are four principal +classes of food stored in seeds: _sugars_, _starches_, _oils_, and +_proteins_. The first are held in solution and can be detected, if +in sufficient quantity, by the taste. The most important varieties +of this group are cane and grape sugar, the latter occurring most +abundantly in fruits, the former in roots and stems. Oil usually +occurs in the form of globules. It is very abundant in some seeds, +_e.g._ flax, castor bean, and Brazil nut. In the corn grain it is +found in the part constituting the germ, or embryo (Figs. 6, 7). +Starches and proteins occur in the form of small granules, which have +specific shapes in different plants (Figs. 8, 9). Those containing +proteins are called _aleurone_ grains, and are, as a rule, smaller +than the starch grains with which they are intermixed in the bean +and some other seeds. In wheat, corn, rice, and most grains they +form a layer just inside the husk, as shown in Fig. 10. This is the +reason why polished rice and finely bolted flour are less nutritious +than the darker kinds, from which this valuable food substance has +not been removed. The two most familiar kinds of proteins are the +_albumins_, of which the white of an egg is a well-known example, and +the _glutins_, which give to the dough of wheat flour and oatmeal +their peculiar gummy or “glutinous” structure. + +[Illustration: FIGS. 8-9.—Different forms of starch grains: 8, rice; +9, wheat.] + +=4. Organic foods.=—These four substances, starch, sugar, fats, and +proteins, with some others of less frequent occurrence, are called +_organic foods_, because they are produced, in a state of nature, +only through the action of organized living bodies, or, more strictly +speaking, of living vegetable bodies. + +[Illustration: FIG. 10.—Transverse section near the outside of a +wheat grain: _e_, the husk; _a_, cells containing protein granules; +_s_, starch cells (_after_ Tschirch).] + +=5. Our dependence upon plants.=—While the animal organism can digest +and assimilate these substances after they have been formed by +plants, it has no power to manufacture them for itself, and, so far +as we know at present, is wholly dependent upon the vegetable world +for these necessaries of life. In one sense the whole animal kingdom +may be said to be parasitic on plants. The wolf that eats a lamb is +getting his food indirectly from the grains and grasses consumed by +its victim, and the lion that devours the wolf that ate the lamb is +only one step further removed from a vegetable diet. + +=6. The vegetable cell.=—If you will break open a well-soaked horse +bean and examine the contents with a lens, you will see that they +are composed of small oval or roundish granules packed together +like stones in a piece of masonry. These little bodies, called +_cells_, are the ultimate units out of which all animal and vegetable +structures are built up, as a wall is built of bricks and stones. +They differ very much from bricks and stones, however, in that they +are, or have been, living structures with their periods of growth, +activity, decline, and death, just like other living matter, as +will be seen by and by, when we come to look more particularly into +their life history. They consist usually of an inclosing membrane +which contains a living substance called _protoplasm_. This is the +essential part of the cell, and, so far as we know at present, the +physical basis of all life. Cells are commonly more or less rounded +in shape, though they take different forms according to the purpose +they serve. Sometimes, as in the fibers of cotton and the down of +young leaves, they are long and hairlike; when closely packed, they +often become angular by pressure, like those shown in Figs. 10, 11. +The cells composing the thick body of the bean are for the most +part starch and other substances stored up for food, which render +observation difficult. It will, therefore, be better to choose for a +study of the individual cell some kind that will show the essential +parts more distinctly. + +[Illustration: FIG. 11—Typical cells: _n_, nucleus; _p_, protoplasm; +_w_, cell wall; _s_, sap.] + +=7. Microscopic examination of a cell.=—Place under a high power +of the microscope a portion of fresh skin from one of the inside +scales of an onion, or a piece of the root tip of a very young corn +or oat seedling, and fix your attention on one of the individual +cells. Notice (1) the cell wall or inclosing membrane, _w_ (Fig. 11); +(2) the protoplasm, _p_, which may be recognized by its granular +appearance; (3) the _nucleus_, _n_; and (4) the cell sap, _s_. In +very young cells the protoplasm will be seen to fill most of the +interior; but in mature ones, like the large one on the right of the +figure, it forms a thin lining around the wall, with the nucleus +on one side, while the cell sap, composed of various substances in +solution, occupies the central portion. Though there is generally +an inclosing wall, this is not essential, its office being to give +strength and mechanical support by holding the contents together, as +an India-rubber bag holds water. It is the turgidity of the cell, +when distended with liquid, that gives firmness to herbaceous plants +and the tender parts of woody ones. This may be illustrated by +observing the difference between a rubber bag when quite full and +when only half full of water, or a football when partially and when +fully inflated. In its simplest form, however, the cell is a mere +particle of protoplasm, which has one part, constituting the nucleus, +a little more dense in appearance than the rest, but this kind is not +common in vegetable structures. + +=8. How food substances get into the cells.=—As there are no openings +in the cell walls, the only way substances can get into a cell or +out of it is by soaking through the inclosing membrane, as will be +explained in a later chapter. Since starch, oil, and proteins, the +most important foods stored in seeds, are none of them soluble in the +cell sap, it is clear that they could not have got into the cells in +their present state, but must have undergone some change by which +they were rendered capable of passing through the cell wall. + +=9. Digestion.=—The process by which this change is brought about +is known as _digestion_, from its similarity to the same function +in animals. Not only are foods, in the state in which we find them +stored in the seed, incapable of passing through the cell wall, +but the protoplasm, the living part of the cell, has no power to +assimilate and to utilize these substances as food until they have +been reduced to a soluble form in which they can be diffused freely +from cell to cell through any part of the plant. By _diffusion_ is +meant the gradual spread of soluble substances through the containing +medium, as when a lump of sugar or salt, dropped into a glass of +water, dissolves and slowly diffuses through the contents, imparting +a sweet or salty taste to the whole. + +[Illustration: FIG. 12.—Starch grains of wheat in different stages of +disintegration under the action of a ferment (diastase), accompanying +germination: _a_, slightly corroded; _b_, _c_, and _d_, more advanced +stages of decomposition.] + +During the process of digestion the different kinds of food are +acted upon and made soluble by certain chemical ferments, which are +secreted in plants for the purpose. The digestion of starch, the most +abundant of plant foods, is effected by diastase, a common ferment +obtained from germinating grains of barley, wheat, corn, rice, etc. +By the presence of diastase starch is converted into grape sugar, +a substance which is readily soluble in water, and which can be +diffused easily through the tissues of the plant to any part where it +is needed. In this way food travels from the leaf, where it is made, +to the seed, where the sugar is generally reconverted into starch and +stored up for future use, though sometimes, as in the sugar corn and +sugar pea, it remains in part unchanged. The kernels of this kind of +corn can be distinguished readily from those of the ordinary starch +corn, after maturity, by their wrinkled appearance, owing to their +greater loss of water in drying. + +=10. Food tests.=—In order to tell whether any of the food substances +named occur in the seeds that we are going to examine, it will be +necessary to understand a few simple tests by which their presence +may be recognized. The chemicals required can be ordered ready for +use from a druggist or may be prepared in the laboratory as needed, +according to the directions given. Write in your notebook a brief +account of each experiment made, with the conclusions drawn from it. + + EXPERIMENT 1. TO DETECT THE PRESENCE OF FATS.—Rub a small lump of + butter or a drop of oil on a piece of thin white paper. What is the + effect? + + EXPERIMENT 2. ANOTHER TEST FOR FATS.—Place some macerated alcanna + root in a vessel with alcohol enough to cover it, and leave for + an hour. Add an equal bulk of water and filter. The solution will + stain fats, oils, and resins deep red. + +[Illustration: PLATE 2.—Carrying water over the Mississippi levee +by siphon to irrigate rice fields. (_From_ Circular of La. Exp. +Station.)] + + EXPERIMENT 3. TO SHOW THE PRESENCE OF STARCH.—Put a drop of iodine + solution on some starch. What change of color takes place? To + make iodine solution, add to one part of iodine crystals 4 parts + potassium iodide and 95 parts water. It should be kept in the + dark, as light decomposes it. Iodine colors starch blue, protein + substances light brown. In testing for starch, the solution should + be diluted till it is of a pale color, otherwise the stain will be + so deep as to appear black. + + EXPERIMENT 4. A TEST FOR PROTEINS.—Place a small quantity of the + white of an egg, diluted with water, in a clean glass and add a few + drops of nitric acid; or drop some of the acid on the white of a + hard-boiled egg. What is the effect? + + Nitric acid turns proteins yellow; if the color is indistinct, add + a drop of ammonia, when an orange color will ensue. + + EXPERIMENT 5. ANOTHER TEST FOR PROTEINS.—Place on the substance to + be examined a drop of a saturated solution of cane sugar and water; + add a drop of pure sulphuric acid; if proteins are present, they + will be colored red. See also Exp. 3. + + EXPERIMENT 6. A TEST FOR GRAPE SUGAR.—Heat a teaspoonful of + Fehling’s Solution to the boiling point in a test tube (a common + glass vial can be used by heating gradually in water) and pour in a + few drops of grape sugar solution. Heat again and observe the color + of the precipitate that forms. + + Fehling’s Solution may be obtained of the druggist, or, if + preferred, it may be prepared in the laboratory as follows: (_a_) + Dissolve 173 grams of crystallized Rochelle salts and 125 grams + of caustic potash in 500 cc. of water; (_b_) dissolve 34.64 grams + crystallized copper sulphate in 500 cc. of water, and mix equal + parts as needed. (For English equivalents, see Appendix, Weights + and Measures.) The two mixtures must be kept separate till wanted + for use, or prepared fresh as needed. + + Grape Sugar causes Fehling’s Solution to form a red precipitate. + + EXPERIMENT 7. TO SHOW THE DIFFERENCE BETWEEN SUGAR AND STARCH IN + REGARD TO SOLUBILITY.—Mix some sugar with water and notice how + readily it dissolves. Try the same experiment with starch and + observe its different behavior. + + EXPERIMENT 8. TO SHOW HOW STARCH IS DISINTEGRATED IN THE ACT OF + DIGESTION.—Place a few grains of starch on a slide, add a drop or + two of diastase solution, and observe under the microscope; the + starch granules will be seen to disintegrate and melt away. Even + with a hand lens it can be seen, from the greater clearness of the + liquid in comparison with a mixture of untreated starch and water, + that the grains have been dissolved. + + EXPERIMENT 9. TO SHOW THAT DIASTASE CONVERTS STARCH INTO + SUGAR.—Make a paste of boiled starch so thin that it looks like + water. Pour a small quantity of it into each of two tubes, adding a + little diastase to one and leaving the other untreated. Keep in a + warm place for twenty-four hours, then test both tubes for starch, + as directed in Exp. 3, and note the result. If the diastase has not + acted, add a little more and watch. + + + Practical Questions + + 1. Name all the food and other economic products you can think of + that are derived from the seed of maize; from wheat; from flaxseed; + from cotton. + + 2. Mention some seeds from which medicines are procured. + + 3. Name all the seeds you can think of from which oil is obtained; + starch; some that are rich in proteins. (Exps. 1-5.) + + 4. Describe some of the ways in which these products are frequently + adulterated. + + 5. If you were raising corn to sell to a starch factory, what part + of the seed would you seek to develop? If to feed stock, what part? + Why, in each case? (3; Figs. 4-7.) + + 6. What grain feeds more human beings than does any other? + + 7. Name all the seeds you can think of that contain sugar in + sufficient quantity to be detected without chemical tests; that is, + by tasting alone. + + 8. Is “coal oil” a mineral or an organic substance? Explain, by + giving an account of its origin. + + 9. What is gluten? (3.) Name some grains that are especially rich + in it. + + 10. Which of our three chief food grains is a water plant? (See + Plate 2.) Which grows farthest south? Which farthest north? Which + one is of American origin? + + + II. SOME PHYSIOLOGICAL PROPERTIES OF SEEDS + + MATERIAL.—Seeds of squash, pumpkin, or other melon; castor bean; + any kind of common kidney bean; grains of Indian corn. + + APPLIANCES.—In the absence of gas, an alcohol or kerosene lamp may + be used for heating. A double boiler can easily be made by using + two tin vessels of different sizes. Partly fill the larger one with + water, set in it the smaller one with the substance to be heated, + and place over a burner. A pair of scales, a strong six-ounce + bottle, wire-netting, cord, and wax or paraffin should be provided. + + EXPERIMENT 10. DO SEEDS IN THEIR ORDINARY QUIESCENT STATE CONTAIN + ANY WATER?—Place a number of beans, or grains of corn or wheat in + a glass bottle, making a small perforation in the cork to allow + the air to escape, and heat gently. Does any moisture form on the + glass? + + A better test is to weigh two or three ounces of seeds, and heat + them in a double boiler or in oil to prevent scorching. Weigh at + intervals. If there is any loss of weight, to what is it due? + + EXPERIMENT 11. DO SEEDS ABSORB WATER?—Soak a number of beans or + grains of corn in water for 12 to 24 hours and compare with dry + ones. What difference do you notice? To what cause is it due? + + EXPERIMENT 12. HOW DID WATER GET INTO THE SOAKED SEEDS?—Dry gently + with a soft cloth some of the seeds used in the last experiment and + press them lightly to see if water comes out, and where. Place a + number of dry seeds of different kinds—squash, bean, castor bean, + quince, etc.—in warm water and notice whether any bubbles of air + form on them and at what point. Examine with a lens and see if this + point differs in any way from the rest of the seed cover. Does it + correspond with the point from which water exuded in the soaked + seeds? Could hard seeds like the squash, castor bean, buckeye, and + Brazil nut get water readily without an opening somewhere in the + coat? + + EXPERIMENT 13. TO FIND OUT WHETHER WATER IS ABSORBED THROUGH THE + SEED COATS.—Place in moist sand or sawdust two rows of beans as + nearly as possible of the same size and weight, with the eye + pressed down to the substratum in one row and turned up in the + other, so that no moisture can enter through it. In the same way + arrange two rows of castor beans with the little end down in one + row and uppermost in the other. In the last set carefully break + away the spongy mass near the tip, without injuring the parts about + it. Watch and see in which rows water is absorbed most readily. + What change takes place in the spongy masses at the tips of those + castor beans on which they were left? + +[Illustration: FIG. 13.—Effect of the expansion of seeds due to +absorption of water.] + + EXPERIMENT 14. IS THE RATE OF GERMINATION AFFECTED BY THE PRESENCE + OR ABSENCE OF OPENINGS?—Seal up with wax or paraffin all the + openings of a number of air-dry peas or beans, and leave an equal + number of the same size and weight untreated. Be careful that the + sealing is absolutely water-tight, since otherwise the experiment + will be worthless. Plant both sets and keep under like conditions + of soil, temperature, and moisture. Do you see any difference in + the rate of germination of the two sets? + + EXPERIMENT 15. DO SEEDS EXERT FORCE IN ABSORBING WATER?—Fill a + common six-ounce bottle as full as it will hold with dry peas, + beans, or grains of corn; then pour in water till the bottle is + full. Tie a piece of wire-netting or stout sackcloth over the top + to keep the seeds from being forced out. Bind both the neck and the + body of the bottle tightly with strong cords encircling it in both + a horizontal and vertical direction, and place under water in a + moderately warm temperature. Watch for results. + + EXPERIMENT 16. IS THE FORCE EXERTED IN THE LAST EXPERIMENT A + MERELY MECHANICAL ONE, LIKE THE BURSTING OF A WATER PIPE, OR IS IT + PHYSIOLOGICAL AND THUS DEPENDENT ON THE FACT THAT THE SEEDS ARE + ALIVE?—To answer this question try Exp. 15 with seeds that have + been killed by heat or by soaking in formalin. + + + Practical Questions + + 1. Will a pound of pop corn weigh as much after being popped as + before? (Exp. 10.) + + 2. What causes the difference, if there is any? (Exp. 10.) + + 3. Does the tuft of downy hairs at the tip of wheat and oat grains + influence their water supply? The spongy covering of black walnuts + and almonds? The pithy inside layers of pecans and English walnuts? + (Exps. 12, 13.) + + 4. Why will seeds, as a general thing, germinate more readily after + being soaked? (Exps. 11, 14, 16.) + + + III. TYPES OF SEEDS + + MATERIAL.—Dry and soaked grains of corn, wheat, or oats; bean, + squash, castor bean, and pine seed, or any equivalent specimens + showing the differences as to number of cotyledons and the + presence or absence of endosperm. Each student should be provided + with several specimens, both soaked and dry, of the kind under + consideration. Corn, beans, and wheat need to be soaked from 12 + to 24 hours; squash and pumpkin from 2 to 5 days, and very hard + seeds, like the castor bean and morning-glory, from 5 to 10. If + such seeds are _clipped_, before soaking, that is, if a small piece + of the coat is chipped away from the end opposite the scar, or eye, + they will soften more quickly. Keep them in a warm place with an + even temperature till just before they begin to sprout, when the + contents become softened. Very brittle cotyledons may be softened + quickly by boiling for a few minutes. + + No appliances are needed beyond the pupil’s individual outfit and + some of the food tests given in Section I of this chapter. + +=11. Dissection of a grain of corn.=—Examine a dry grain of corn +on both faces. What differences do you notice? Sketch the grooved +side, labeling the hard, yellowish outer portion, _endosperm_, the +depression near the center, _embryo_, or _germ_. + +Next take a grain that has been soaked for twenty-four hours. What +changes do you see? How do you account for the swelling of the +embryo? Remove the skin and observe its texture. Make an enlarged +sketch of a grain on the grooved side with the coat removed, labeling +the flat oval body embedded in the endosperm, _cotyledon_; the upper +end of the little budlike body embedded in the cotyledon, _plumule_, +the lower part, _hypocotyl_—words meaning, respectively, “seed leaf,” +“little bud,” and “the part under the cotyledon.” As this part has +not yet differentiated into root and stem, we cannot call it by +either of these names. The cotyledon, hypocotyl, and plumule together +compose the embryo. Pick out the embryo and sketch as it appears +under the lens. Crush it on a piece of white paper; what does it +contain? + +[Illustration: FIGS. 14-16.—Dissection of a grain of corn: 14, soaked +grain, seen flatwise, cut away a little and slightly enlarged, so as +to show the embryo lying in the endosperm; 15, in profile section, +dividing the grain through the embryo and cotyledon; 16, the embryo +taken out whole. The thick mass is the cotyledon; the narrow body +projecting upwards, the plumule; the short projection at the base, +the hypocotyl (_after_ GRAY).] + +Make a vertical section of another soaked grain at right angles to +its broader face, and sketch, labeling the parts as they appear in +profile. Make a cross section through the middle of another grain and +sketch, labeling the parts as before. What proportion of the grain is +endosperm and what embryo? Put a drop of iodine and of nitric acid +separately on pieces of the endosperm, and note the effects. Test the +seed coats and the cotyledon to see if they contain any starch. + +Notice that the corn grain has but one cotyledon, hence such seeds +are said to be _monocotyledonous_, or one-cotyledoned. The grains are +not typical seeds, but are selected for examination because they are +large and easy to handle, can be obtained everywhere, and germinate +readily. + +=12. Dissection of a bean.=—Sketch a dry bean as it lies in the pod, +showing its point of attachment and any markings that may appear on +its surface. Then take it from the pod and examine the narrow edge +by which it was attached. Notice the rather large scar (commonly +called the eye of the bean) where it broke away from the point of +attachment. This is the _hilum_. Near the hilum, look for a minute +round pore like a pinhole. This is called the _micropyle_, from a +Greek word meaning “a little gate,” because it is the entrance to +the interior of the seed coat. There was no micropyle observed in +the corn grain, because it is not a true seed but a fruit inclosing +a single seed. The inclosing membrane is the fruit skin, which has +become incorporated with the seed coat and taken its place as a +protective covering. Compare a soaked bean with a dry one; what +difference do you perceive? How do you account for the change in size +and hardness? Find the hilum and the micropyle in the soaked bean. +Lay it on one side and sketch, with the micropyle on top; then turn +toward you the narrow edge that was attached to the pod and sketch, +labeling all the parts. Make a section through the long diameter at +right angles to the flat sides, press it slightly open, and sketch +it. Notice the line or slit that seems to cut the section in half +longitudinally, and the small round object between the halves at one +end; can you tell what it is? + +[Illustration: FIGS. 17, 18.—A kidney bean: 17, side view; 18, front +view, showing _h_, hilum, _m_, micropyle.] + +[Illustration: FIG. 19.—Cotyledon of a bean, showing plumule.] + +Slip off the coat from a whole bean and notice its texture. Hold it +up to the light and see if it shows any signs of veining. See whether +the scar at the hilum extends through the kernel, or marks only the +seed coat. Lay open the two flat bodies into which the kernel divides +when stripped of its coats, keeping them side by side, with the part +above the micropyle toward the top. Sketch their inner face and +label them _cotyledons_. Be careful not to break or displace the +tiny bud packed away between the cotyledons, just above the hilum. +Label the round portion of this bud, _hypocotyl_, and the upper, more +expanded part, _plumule_. Which way does the base of the hypocotyl +point; toward the micropyle, or away from it? Pick out this budlike +body entire and sketch as it appears under the lens. Open the plumule +with a pin and examine it with a lens; of what does it appear to +consist? Do you find any endosperm around the cotyledons, as in the +corn and oats? Break one of the soaked cotyledons, apply the proper +tests (Exps. 2, 3, 5), and report what substances it contains. Where +is the nourishment for the young plant stored? What part of the bean +gives it its value as food? + +Notice that in the bean the embryo consists of three parts, the +hypocotyl, plumule, and the two cotyledons, which completely fill +the seed coats, leaving no place for endosperm. Seeds like the bean, +squash, and castor bean, which have two cotyledons, are said to be +_dicotyledonous_. + +=13. The castor bean.=—Lay a castor bean on a sheet of paper before +you with its flat side down; what does it look like? The resemblance +may be increased by soaking the seed a few minutes, in order to swell +the two little protuberances at the small end. Can you think of any +benefit a plant might derive from this curious resemblance of its +seed to an insect? + +Sketch the seed as it lies before you, labeling the protuberance +at the apex, _caruncle_. The caruncle is an appendage of the +seed-covering developed by various plants; its use is not always +clear. What appears to be its object in the castor bean? Refer to +Exp. 13 and see if there is any other purpose it might serve. + +Turn the seed over and sketch the other side. Notice the colored +line or stripe that runs from the large end to the caruncle. This +is the _rhaphe_, and shows the position that would be occupied by +the seed stalk if it were present. Its starting point near the large +end, which is marked in fresh seeds by a slight roughness, is the +_chalaza_, or organic base of the seed, where the parts all come +together like the parts of a flower at their insertion on the stem. +Where was it situated in the common bean? How does this differ from +its position in the castor bean? Where the rhaphe ends, just at the +beak of the caruncle, you will find the hilum. The micropyle is +covered by the caruncle, which is an outgrowth around it. + +[Illustration: FIGS. 20-22.—Castor bean (slightly magnified); +20, back view; 21, front view; _ch_, chalaza; _r_, rhaphe; _ca_, +caruncle; 22, vertical section; _en_, endosperm; _cc_, cotyledons; +_hy_, hypocotyl; _hi_, hilum; _m_, micropyle.] + +Now cut a vertical section through a seed that has been soaked +for several days, at right angles to the broad sides, and sketch +it. Label the white, pasty mass within the seed coats, endosperm. +Can you make out what the narrow white line running through the +center of the endosperm, dividing it into two halves, represents? +Make a similar sketch of a cross section. Notice the same white +line running horizontally across the endosperm, dividing it into +two equal parts. To find out what these lines are, take another +seed (always use soaked seeds for dissection) and remove the coats +without injuring the kernel. Split the kernel carefully round the +edges, remove half the endosperm, and sketch the other half with the +delicate embryo lying on its inner face. You will have no difficulty +now in recognizing the lines in your drawings as sections of the +thin cotyledons. Where is the hypocotyl, and which way does its base +point? Remove the embryo from the endosperm, separate the cotyledons +with a pin, hold them up to the light, and observe their beautiful +texture. Sketch them under the lens, showing the delicate venation. +Is there any plumule? + +Test the endosperm with a little iodine. Does it give a blue or a +brown reaction? Crush another bit of it on a piece of white paper and +see if it leaves a grease spot. What does this show that it contains? +Test the embryo in the same way, and see whether it contains any oil. + + NOTE.—It should be borne in mind that the castor bean bears no + relation whatever to the true beans. It belongs to the spurge + family, which is botanically very remote from that of the peas and + beans. + +[Illustration: FIGS. 23-25.—Seed of a squash; 23, seed from the +outside; 24, vertical section perpendicular to the broad side; +25, section parallel to the broad side, showing inner side of a +cotyledon; _a_, seed coat; _c_, cotyledons; _h_, hypocotyl; _p_, +plumule.] + +=14. Study of a squash or gourd seed.=—How does the coat of a squash +seed differ from that of the bean? At the small end, look for two +dots, or pinholes, close together. Refer to your drawing of the bean +and see if you can make out, with the help of a lens, what they are. +The bean is a curved seed, which is bent so as to bring the hilum +close to the micropyle on one side. But by far the greater number +of seeds are _inverted_, or turned over on their stalks, as you +sometimes see huckleberry blossoms and bell flowers on their stems, +so that when the stalk breaks away from its attachment, the scar and +the micropyle come close together at one end, as in the squash seed. + +[Illustration: FIG. 26.—Diagram of an inverted or anatropous seed, +showing the parts in section: _a_, outer coat; _b_, inner coat; +_c_, kernel; _d_, rhaphe; _ch_, chalaza; _h_, hilum; _m_, micropyle +(_After_ GRAY).] + +Make a drawing of the outside of a seed, labeling all the parts you +have observed; then gently remove the hard coat, or _testa_, as it +is called. The thin, greenish covering that lines it on the inside +is the endosperm. How does it compare in quantity with that in the +corn and castor bean? How do the cotyledons compare in thickness +with those of the bean? Carefully separate them and draw, labeling +the parts as you make them out. The tiny pointed object between the +cotyledons at their point of union is the plumule; is it as well +developed as in the bean? Can you see any reason why seeds like the +pea and bean, which have cotyledons too thick and clumsy to do well +the work of true leaves, should have a well-developed plumule, while +those with thin cotyledons, like the squash and pumpkin, do not, +as a general thing, form a large plumule in the embryo? The little +projection in which the cotyledons end is the hypocotyl; which way +does it point? Where did you find the micropyle to be? Test the +cotyledons and some of the endosperm for food substances; what do you +find in them? + +=15. Study of a pine seed.=—Remove one of the scales from a pine cone +and sketch the seed as it lies in place on the cone scale. Notice +its point of attachment to the scale, and look near this point for a +small opening, which you can easily recognize as the micropyle. The +seed with its wing looks very much like a fruit of the maple, but +differs from it in being a naked seed borne on the inner side of a +cone scale, without a pod or husk or outer covering of any kind, such +as beans and nuts and grains are provided with. Plants like the pine, +which bear their seed in this way, are called _Gymnosperms_, a word +that means “naked seeds,” in contradistinction to the _Angiosperms_, +which bear their seeds in pods or other closed envelopes. + +[Illustration: FIGS. 27, 28.—Pitch pine seeds: 27, scale, or open +carpel, with one seed in place; 28, winged seed, removed. (_After_ +GRAY.)] + +[Illustration: FIG. 29.—Section of pine seed, showing the +polycotyledonous embryo (GRAY).] + +Remove the coat from a seed that has been soaked for twenty-four +hours, and examine it with a lens. Does it consist of one or more +layers? Is there any difference in color between the inner and outer +layers? Look at the base of the hypocotyl for some loose, cobwebby +appendages. These are the remains of other embryos with certain +appendages belonging to them that were formed in the endosperm, but +failed to develop. Did you find remains of this kind in any of the +other seeds examined? Pick out the embryo from the endosperm and +test both for food substances. Which of these do you find? Which +are absent? How does the embryo differ from those already examined? +How many cotyledons are there? Make an enlarged sketch of a seed in +longitudinal section, labeling correctly all the parts observed. + +=16. Comparison as to food value of seeds.=—Make in your notebook a +tabular statement after the model here given, of the food contents +found in the different seeds you have examined. Indicate the relative +quantity of each by writing under it, in the appropriate column, the +words, “much,” “little,” or “none,” as the case may be. + + + MODEL FOR RECORD OF SEEDS EXAMINED + + +================+===========================================+ + | | FOODS TESTED | + | SEEDS EXAMINED +----------+----------+----------+----------+ + | | Starch | Sugar | Oil | Proteins | + +----------------+----------+----------+----------+----------+ + | Corn | | | | | + +----------------+----------+----------+----------+----------+ + | Wheat | | | | | + +----------------+----------+----------+----------+----------+ + | Bean | | | | | + +----------------+----------+----------+----------+----------+ + | Squash | | | | | + +----------------+----------+----------+----------+----------+ + | Castor bean | | | | | + +----------------+----------+----------+----------+----------+ + | Pine | | | | | + +----------------+----------+----------+----------+----------+ + +By far the greater number of seeds contain endosperm; that is, they +consist of an embryo with more or less nourishing matter stored +about it. Even in seeds which appear to have none, the endosperm is +present at some period during development, but is absorbed by the +cotyledons before germination. + +=17. Manner of storing nourishment.=—In the various seeds examined, +we have seen that the nourishment for the young plant is either +stored in the embryo itself, as in the cotyledons of the bean, acorn, +squash, etc., or packed about them in the form of endosperm, as in +the corn, wheat, and castor bean. + +=18. The number of cotyledons.=—Seeds are also classed according +to the number of their cotyledons, as having one, two, or many +cotyledons. The first two kinds make up the great class of +Angiosperms, which includes all the true flowering plants and forms +the most important part of the vegetation of the globe. The last +is characteristic of the great natural division of Gymnosperms, or +naked-seeded plants, of which we have had an example in the pine. +They are the most primitive type of living seed-bearing plants. +Though they are not so abundant now as in past ages, numbering only +about four hundred known species, they present many diversities of +form, which seem to ally them on the one hand with the lower, or +spore-bearing plants (ferns, mosses, etc.), and on the other hand +with the Angiosperms. + + + Practical Questions + + 1. Make a list of all the seeds you can find that have very thick + cotyledons, and underline those that are used as food by man or + beast. + + 2. Make a similar list of all the kinds with thin cotyledons and + more or less endosperm, that are used for food or other purposes. + + 3. Do you find a greater number of foodstuffs among the one kind + than the other? + + 4. How do the two kinds compare, as a general thing, in size and + weight? + + 5. From what part of the castor bean do we get oil? of the peanut? + of cotton seed? (Exps. 1-6.) + + 6. Is there any valid objection to the wholesomeness of peanut oil, + and of cottonseed lard as compared with hog’s lard? (1, 3.) + + 7. What is bran? Does it contain any nourishment? (11, 12; Exps. + 1-6.) + + 8. What gives to Indian corn its value as food? to oats? wheat? + rice? (3; Exps. 1-6.) + + 9. Which of these grains has the larger proportion of endosperm to + embryo? (Figs. 1-3.) + + 10. Which contains the larger amount of starch in proportion to its + bulk, rice or Indian corn? + + 11. If you wished to produce a variety of corn rich in oil, you + would select seed for planting with what part well developed? (3; + Figs. 4-7.) + + + IV. SEED DISPERSAL + + MATERIAL.—Fruits and seeds of any kind that show adaptations for + dispersal. Some common examples are: (1) Wind: ash, elm, maple, + ailanthus, milkweed, clematis, sycamore, linden, dandelion, + thistle, hawkweed. (2) Water: pecan, filbert, cranberry, lotus, + hickory nut, coconut—obtain one with the husk on, if possible. (3) + Animal agency (involuntary): cocklebur, tickseed, beggar-ticks, + burdock; (voluntary) almost all kinds of edible fruits, especially + the bright-colored ones—wild plums, cherries, haws, dogwood, + persimmons, etc. (4) Explosive and self-planting: witch-hazel, + wood sorrel, violet, crane’s-bill, wild vetch, peanut, medick, + stork’s-bill (Erodium). + + EXPERIMENT 17. TO SHOW HOW SEEDS ARE DISPERSED BY WIND.—Take a + number of winged and plumed fruits and seeds, such as those of the + maple, ash, ailanthus, dandelion, clematis, milkweed, and trumpet + creeper; stand on a chair or table in a place where there is a + draft of air and let them all go. Which travel the farther, the + winged or the plumed kinds? Which sort is better fitted to aërial + transportation? + + EXPERIMENT 18. DISPERSAL BY WATER.—Place in a bucket of water a + hazelnut, an acorn, an orange, a cranberry, a pecan, a hickory nut, + a fresh apple, and a coconut with the husk on. Which are the best + floaters? Cut open or break open the good swimmers, compare with + the non-floaters, and see to what peculiarity of structure their + floating qualities are due. In what situations do the cranberry and + the coconut grow? Can you see any advantage to a plant so situated + in producing fruits that float easily? + + EXPERIMENT 19. DISPERSAL BY EXPLOSIVE CAPSULES.—Moisten slightly + some mature but unopened capsules of witch hazel, wood sorrel, + rabbit pea, or violet, and leave in a warm, dry place for fifteen + to forty-five minutes. What happens when the pods begin to dry? + Measure the distance to which the different kinds of seeds have + been ejected. Which were thrown farthest? What was the object of + the movement? What caused the explosion? + + EXPERIMENT 20. THE USE OF ADHESIVE FRUITS.—Scatter broadcast + a handful of hooked or prickly seeds or fruits—cocklebur, + tickseed, beggar-ticks, bur grass, etc. Are they suited for wind + transportation? Drop one of them on your sleeve, or on the coat + of a fellow student; will it stay there? What would be the effect + if it became attached to the fur of a roaming animal? Is this a + successful mode of dissemination? + +[Illustration: FIGS. 30-32.—30, A pod of wild vetch, with mature +valves twisting spirally to discharge the seed; 31, pod of +crane’s-bill discharging its seed; 32, capsules of witch-hazel +exploding.] + +[Illustration: FIGS. 33-36.—Fruits adapted to wind dispersal: 33, +winged pod of pennycress; 34, spikelet of broom sedge; 35, akene of +Canada thistle; 36, head of rolling spinifex grass.] + +=19. Agencies of dispersal.=—The means at nature’s disposal for this +purpose, as shown by the experiments just made, are four; namely, +wind, water, the explosion of capsules due to the withdrawal of +water, and the agency of animals, including man. The first three +are purely mechanical. The last, animal agency, is either voluntary +or involuntary, according as it is conscious and intentional, or +accidental merely. Man, of course, is the only consciously voluntary +agent. Of the four agencies named, animals and wind are the most +effective, and the greater number of adaptations observed will be +found to have reference to these. + +[Illustration: FIG. 37.—Good quality of clover seed.] + +[Illustration: FIG. 38.—Inferior quality of clover seed mixed with +“screenings.”] + +[Illustration: FIG. 39.—Dodder on red clover, showing how the seeds +get mixed.] + +=20. Involuntary dispersal.=—The lower animals may be voluntary +agents in a way, though not designedly so, as when a squirrel buries +nuts for his own use and then forgets the location of his hoard and +leaves them to germinate; or when a jaybird flies off with a pecan +in his bill, intending to crack and eat it, but accidentally lets +it fall where it will sprout and take root. Both man and the lower +animals are not only involuntary, but often unwilling agents of +dispersal. Some of the most troublesome weeds of civilization have +been unwittingly distributed by man as he journeyed from place to +place, carrying, along with the seed for planting his crops, the +various weed seeds, or “screenings,” as these mixtures are called +by dealers, with which they have been adulterated either through +carelessness and ignorance, or from unavoidable causes. The neglected +animals, also, that are allowed by short-sighted farmers to wander +about with their hair full of cockleburs and other adhesive weed +pests, are no doubt very unwilling carriers of those disagreeable +burdens. + +=21. Tempting the appetite.=—This is the most important adaptation +to dispersal by animals. Have you ever asked yourself how it could +profit a plant to tempt birds and beasts to devour its fruit, as so +many of the bright berries we find in the autumn woods seem to do? To +answer this question, examine the edible fruits of your neighborhood +and you will find that almost without exception the seeds are hard +and bony, and either too small to be destroyed by chewing, and +thus capable of passing uninjured through the digestive system of +an animal; or, if too large to be swallowed whole, compelling the +animal, by their hardness or disagreeable flavor, to reject them. +In cases where the seeds themselves are edible and attractive, the +fruits are usually armed during the growing season with protective +coverings, like the bur of the chestnut and the astringent hulls +of the hickory nut and walnut. The acidity or other disagreeable +qualities of most unripe fruits serves a similar purpose, while their +green color, by making them inconspicuous among the foliage leaves, +tends still further to insure them against molestation. + +[Illustration: FIGS. 40-42.—Adhesive fruits: 40, fruit of +hound’s-tongue; 41, akene of bur marigold; 42, fruit of bur grass +(cenchrus).] + +=22. Voluntary agency.=—The cultivated fruits and grains owe their +distribution and survival almost entirely to the voluntary agency +of man. Dispersal by this means, whether intentional or accidental, +is purely artificial, and except in the case of a few annuals like +horseweed, bitterweed, ragweed, goosefoot, and other field pests that +have adjusted their season of growth and flowering to the conditions +of cultivation, is not correlated with any special modification of +the plants for self-propagation. On the contrary, many of the most +widely distributed weeds of cultivation, such as the oxeye daisy, the +rib grass, mayweed and bitterweed, possess very imperfect natural +means of dispersal, and are largely dependent for their propagation +on the involuntary agency of man. + +=23. Use of the fruit in dispersal.=—It will be seen from the +foregoing observations that the fruit plays a very important part in +the work of dispersal, most of the adaptations for this purpose being +connected with it. In cases where a number of seeds are contained in +a large pod that could not conveniently be blown about by the breeze, +adaptations for wind dispersal are attached to the individual seeds, +as in the willow, milkweed, trumpet creeper, and paulonia; but as a +general thing, adaptations of the seed are for protection, the work +of dispersal being provided for by the fruit. In the case of the +large class of plants known as “tumbleweeds,” the whole plant body is +fitted to assist in the work of transportation. Such plants generally +grow in light soils and either have very light root systems, or are +easily broken from their anchorage and left to drift about on the +ground. The spreading, bushy tops become very light after fruiting, +so as to be easily blown about by the wind, dropping their seeds +as they go, until they finally get stranded in ditches and fence +corners, where they often accumulate in great numbers during the +autumn and winter. + +[Illustration: FIG. 43.—A fruiting plant of winged pigweed +(_Cycloloma_), showing the bunchy top and weak anchorage of a typical +tumbleweed.] + +[Illustration: FIG. 44.—Panicle of “old witch grass,” a common +tumbleweed.] + +=24. The advantages of dispersal.=—Seed cannot germinate unless +they are placed in a suitable location as to soil, moisture, and +temperature. In order to increase the chances of securing these +conditions, it is clearly to the advantage of a species that its +seeds should be dispersed as widely as possible, both that the +seedlings may have plenty of room, and that they may not have to draw +their nourishment from soil already exhausted by their parents. The +farmer recognizes this principle in the rotation of crops, because +he knows that successive growths of the same plant will soon exhaust +the soil of the substances required for its nutrition, while they may +leave it richer in nourishment for a different crop. + +[Illustration: FIG. 45.—Self-planting pod of peanut.] + +=25. Self-planting seeds.=—Dispersal is not the only problem the +seed has to meet. The majority of seeds cannot germinate well on +top of the ground, and must depend on various agencies for getting +under the soil. Some of them do this for themselves. The seeds of the +stork’s-bill, popularly known as “filarees,” have a sharp-pointed +base and an auger-shaped appendage at the apex, ending in a +projecting arm (the “clock” of the filaree) by which it is blown +about by the wind with a whirling motion till it strikes a soft +spot, when it begins at once to bore its way into the ground. The +common peanut is another example. The blossoms are borne under the +leaves, near the base of the stem, and as soon as the seeds begin to +form, the flower stalks lengthen several inches, carrying the young +pods down to the ground, where they bore into the soil and ripen +their seeds. + + + Practical Questions + + 1. Name the ten most troublesome weeds of your neighborhood. + + 2. What natural means of dispersal have they? + + 3. Which of them owe their propagation to man? + + 4. Are there any tumbleweeds in your neighborhood? + + 5. Would you expect to find such weeds in a hilly or a well-wooded + region? (19, 23; Exp. 17.) + + 6. What situations are best fitted for their propagation? (19, 23; + Exp. 17.) + + 7. Make a list of all the fruits and seeds you can think of that + are adapted to dispersal by wind; by water; by animals. + + 8. By what means of dissemination, or protection, or both, is each + of the following distinguished: the squash; apple; fig; pecan; + poppy; bean; beggar-tick; linden; grape; rice; pepper; olive; + cranberry; jimson weed; thistle; corn; wheat; oats? + + 9. What is the agent of dispersion, or what the danger to be + provided against, in each case? + + 10. Could our cultivated fruits and grains survive in their present + state without the agency of man? (22.) + + 11. Name all the plants you can think of that bear winged seeds and + fruits; are they, as a general thing, tall trees and shrubs, or low + herbs? + + 12. Name all you can think of that bear adhesive seeds and fruits; + are they tall trees or low herbs? + + 13. Give a reason for the difference. (Exps. 17, 20.) + + 14. Why is the dandelion one of the most widely distributed weeds + in the world? (19; Exp. 17.) + + 15. Is the wool that covers cotton seed for dispersal or protection? + + 16. What advantage to the Indian shot (canna) is the excessive + hardness of its seeds? (21.) + + 17. What is the use to the species, of the bitter taste of lemon + and orange seed? (21.) + + 18. Why are the seeds of dates and persimmons and haws so hard? + (21.) + + 19. Do you find any edible seeds without protection? If so, account + for the want of it. (21, 22.) + + 20. Name some of the agencies that may assist in covering seeds + with earth. + + 21. Do you know of any seeds that bury themselves? + + 22. The seeds of weeds and other refuse found mixed with grain + sold on the market are known, commercially, as “screenings.” Wheat + brought to mills in Detroit showed screenings that contained, among + other things, seeds of black bindweed, green foxtail grass, yellow + foxtail, chess, oats, ragweed, wild mustard, corn cockle, and + pigweed. Can you mention some of the ways in which these foreign + substances may have gotten into the crop and suggest means for + keeping them out? + + + Field Work + + The subjects treated in the foregoing chapter are, in general, + better suited to laboratory than to field work. There are some + details, however, which can be observed to advantage out of doors. + Many of the seeds found in your walks will show peculiarities of + shape and external markings and color that will invite observation. + Examine also the contents of different kinds you may meet with, as + to the presence or absence of endosperm and the arrangement and + development of the embryo. Note: (1) whether, as a general thing, + there is any difference in size and weight and amount of nourishing + matter in the two kinds; (2) the greater variety in the shape and + arrangement of the cotyledons in the albuminous kind, and in the + arrangement of the embryo; (3) the differences in the development + of the plumule in the two kinds,—and give a reason for the facts + observed. + + Among the different seeds you may find, look for adaptations for + dispersal, and decide to what particular method each is suited. + Study the agencies by which various kinds may get covered with + soil. If the common stork’s-bill (_Erodium cicutarium_) grows in + your neighborhood, its seeds will well repay a little study, and if + there is a field of peanuts within reach, do not fail to pay it a + visit. + + + + +CHAPTER II. GERMINATION AND GROWTH + + + I. PROCESSES ACCOMPANYING GERMINATION + + MATERIAL.—A pint or two of corn, peas, beans, or any quickly + germinating seed. + + APPLIANCES.—Matches; wood splinters; gas jet or alcohol lamp; test + tubes; a small quantity of mercuric oxide; a thermometer; a couple + of two-quart preserve jars, and a smaller wide-mouthed bottle that + can be put into one of them; some limewater; a glass tube (the + straws used by druggists for soft drinks will answer). + +=26. Preliminary exercises.=—Before taking up the study of +germinating seeds, it is important to learn from what sources the +organic substances used by the growing plant are derived, and some of +the processes that accompany growth and development. + + EXPERIMENT 21. TO SHOW THE CHANGES THAT ACCOMPANY OXIDATION.—Strike + a match and let it burn out. Examine the burnt portion remaining + in your hand; what changes do you notice? These changes have been + caused by the union of some substance in the match with something + outside of it, in the act of burning; let us see if we can find out + what this outside substance is. + + EXPERIMENT 22. TO SHOW THE ACTIVE AGENT IN OXIDATION.—Heat some + mercuric oxide in a test tube over the flame of a burner. The + heat will cause the oxygen to separate from the mercury, and in a + short time the tube will be filled with the gas. Extinguish the + flame from a lighted splinter and thrust the glowing end into the + tube; what happens? The oxygen unites with something in the wood + and causes it to burn just as the match did. Compare your burnt + splinter with the burnt end of the match; what resemblance do you + notice between them? + + EXPERIMENT 23. TO SHOW THAT CARBON DIOXIDE IS A PRODUCT OF + OXIDATION.—Your experiment with the match showed that ignition + is accompanied by heat, and if active enough, by light, and also + that it left behind a solid substance in the form of charcoal. But + how about the part that united with the oxygen to produce these + results? Let us see what became of it. Hold a lighted candle + under the open end of a test tube, or under the mouth of a small + glass jar. Does any vapor collect on the inside? After two or + three minutes quickly invert the jar or the tube, and thrust in a + lighted match: what happens? Can the substance now in the jar be + ordinary air? Why not? (Exps. 21, 22.) Pour in a small quantity of + limewater, holding your hand over the mouth of the tube to prevent + the air from getting in; the gas inside, being heavier than air, + will not escape immediately unless agitated. What change do you + notice in the limewater? + + It has been proved by experiment that the kind of gas formed by + the burning candle has the property of turning limewater milky; + hence, whenever you see this effect produced in limewater, you may + conclude that this gas, known as _carbon dioxide_, is present; + and conversely, the presence of carbon dioxide, especially if + accompanied by some of the other effects observed, as the giving + out of heat and moisture, may be taken as evidence that some + process similar to that going on in the burning candle is, or has + been, at work. + + EXPERIMENT 24. DO THESE EFFECTS ACCOMPANY ANY OF THE LIFE PROCESSES + OF ANIMALS?—Blow your breath against the palm of your hand; what + sensation do you feel? Blow it against a mirror, or a piece of + common glass; what do you see? Blow through a tube into the bottom + of a glass containing limewater; how is the water affected? How do + these facts correspond with the results of Exp. 23? + + EXPERIMENT 25. IS THERE ANY EVIDENCE THAT A SIMILAR PROCESS GOES ON + IN PLANTS?—(1) Half fill a small, wide-mouthed jar with limewater, + place it inside a larger one (Fig. 46), and fill the space between + them, up to the neck of the smaller vessel, with well-soaked + peas, beans, or barleycorns, on a bed of moist cotton or blotting + paper. Cover with a piece of glass and keep at a moderately warm + temperature. (2) As a control experiment, place beside this another + jar arranged in precisely the same way, except that seeds must + be used whose vitality has been destroyed by heat. To prevent + the entrance of germs among the dead seeds, which might cause + fermentation and thus interfere with the experiment, set the jar + containing them in a vessel of water and boil an hour or two before + the experiment begins. Otherwise, treat precisely as in (1). + +[Illustration: FIG. 46.—Diagrammatic section, showing arrangement +of jars for Exp. 25.] + + After germination has taken place in (1), what change do you notice + in the limewater? If the effect is not apparent, gently stir with a + straw or a glass rod to mix it with the gas in the larger jar. Has + the limewater in the control experiment undergone the same change? + (It may show a slight milkiness due to the carbon dioxide in the + air.) Insert a thermometer among the seeds in both of the larger + jars, and compare their temperature with that of the outside air; + which shows the greater rise? From this experiment and the last + one, what process, common to animals, would you conclude has been + going on in the germinating seeds? + + NOTE.—Heat in germinating seeds is not always due to this cause + alone, but is sometimes increased by the presence of minute + organisms called bacteria. Germinating barley and rye in breweries + sometimes show an increase in temperature of 40 to 70 degrees, due + to these organisms, and spontaneous combustion in seed cotton has + been reported from the same cause. + +=27. Oxidation.=—The process that brought about the results observed +in the foregoing experiments, and popularly known as _combustion_, is +more accurately defined by chemists as _oxidation._ It takes place +whenever substances enter into new combinations with oxygen. The most +familiar examples of it are when oxygen enters into combination with +substances containing carbon. It was the union of a portion of the +oxygen of the air in Exp. 21, and of that in the tube in Exp. 22, +with some of the carbon in the wood, that caused the burning. The +effect was more marked in the second case because the oxygen in the +tube was pure, while in the air it is mixed with other substances. + +=28. Carbon.=—The black substance left in your hand after oxidation +of the wood in Exps. 21 and 22 is _carbon_. It composes the greater +part of most plant bodies, and, in fact, is the most important +element in the realm of organic nature. There is not a living thing +known, from the smallest microscopic germ to the most gigantic tree +in existence, that does not contain carbon as one of its essential +constituents. + +=29. Carbon dioxide.=—The gas produced by the burning candle in Exp. +23, by the germinating seeds in Exp. 25, and expelled from your own +lungs in Exp. 24, is carbon dioxide. Chemists designate it by the +symbol CO₂, which means that it consists of one part carbon to two +parts oxygen. It is an invariable product wherever the oxidation of +substances containing carbon goes on. Heat and moisture are evolved +at the same time, and if oxidation is very active, as in Exps. 21 and +22, light also. When the process takes place very slowly, no light is +evolved, and so little heat as to be imperceptible without special +observation. Hence, oxidation may go on around us and even in our own +bodies without our being conscious of the fact. + +Carbon dioxide is of prime importance to the well-being of plants. It +furnishes the material from which the greater part of their organic +food is derived, as will be seen when we take up the study of the +leaf and its work. To animals, on the contrary, its presence is so +injurious that if the proportion of it in the air we breathe ever +rises much above 1 part to 1000, the ill effects become painfully +sensible. It is not, however, as was formerly supposed, a poison, +the harm it does being to decrease the proportion of oxygen in the +atmosphere so that animals cannot get enough of it to breathe, and +die of suffocation. + +=30. Respiration in plants and in animals.=—It was shown in Exp. +24 that respiration in animals is accompanied by the products of +oxidation; hence we conclude that respiration is a form of oxidation. +And since these same products are given off by plants (Exp. 25), the +inference is clear that the same process goes on in them. But in +plants the life functions are so much more sluggish than in animals +that it is only in their most active state, during germination and +flowering, that evidence of it is to be looked for. + +=31. Respiration and energy.=—In plants, as in animals, respiration +is the expression or measure of energy. Sleeping animals breathe +more slowly than waking ones, snakes and tortoises more slowly than +hares and hawks. The more we exert ourselves and the more vital +force we expend, the harder we breathe; hence, respiration is more +active in children than in older persons and in working people than +in those at rest. It is the same with plants; respiration is most +perceptible in germinating seeds and young leaves, in buds and +flowers, where active work is going on. Hence, in this condition +they consume proportionately larger quantities of oxygen and +liberate correspondingly larger quantities of carbon dioxide, with +a proportionate increase of heat. In some of the arums,—calla lily, +Jack-in-the-pulpit, colocasia, etc.,—and in large heads of compositæ, +like the sunflower, where a great number of small flowers are brought +together within the same protecting envelope, the rise of temperature +is sometimes so marked that it may be perceived by placing a flower +cluster against the cheek. + + + Practical Questions + + 1. What is charcoal? (28.) + + 2. Is any of this substance contained in the seed? in the flour and + meal made from seed? (28; Exp. 25.) + + 3. What combination takes place when the cook lets the stove get + too hot and burns the biscuits? (27, 28.) + + 4. Of what does the burned part consist? (28.) What was it before + it was burned? (27, 28). + + 5. Which burns the more readily, an oily seed or a starchy one? + Which leaves the more solid matter behind? (Suggestion: test by + putting a bean, or a large grain of corn, and an equal quantity + of the kernel of a Brazil nut on the end of a piece of wire and + thrusting into a flame.) + + 6. Is there any rational ground for the statement that the wooden + buildings formerly used on Southern plantations as cotton ginneries + were sometimes destroyed through spontaneous combustion due to the + heat generated by piles of decaying cotton seed? (Exp. 25, Note.) + + + II. CONDITIONS OF GERMINATION + + MATERIAL.—Several ounces each of various kinds of seed. For the + softer kinds, pea, bean, corn, oats, wheat are recommended; for + those with harder coverings, squash, castor bean, apple, pear, or, + where obtainable, cotton; for still harder kinds, persimmon and + date seeds, or the stones of plum and cherry. + + APPLIANCES.—1 dozen common earthenware plates for germinators; 1 + dozen two-ounce wide-mouthed bottles; 2 common glass tumblers; + clean sand, sawdust, or cotton batting, for bedding; a double + boiler; a gas burner, or a lamp stove. + +=32. Recording observations.=—For this purpose a page should be ruled +off in the notebook of each student, after the model here given, +and the facts brought out by the different experiments set down as +observed. + + + NUMBER OF SEEDS GERMINATED + + ==============+=+==+==+==+====+====+====+====+====+=====+==== + No. of hours | |24|48|72|4 d.|5 d.|6 d.|7 d.|8 d.|10 d.|2 w. + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|1| | | | | | | | | | + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|2| | | | | | | | | | + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|3| | | | | | | | | | + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|4| | | | | | | | | | + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|5| | | | | | | | | | + +-+--+--+--+----+----+----+----+----+-----+---- + No. of vessel|6| | | | | | | | | | + ==============+=+==+==+==+====+====+====+====+====+=====+==== + + EXPERIMENT 26. CAN SEEDS HAVE TOO MUCH MOISTURE?—Drop a number + of dry beans or grains of corn, oats, or other convenient seed, + into a vessel with a bedding of cotton or paper that is barely + moistened, and an equal number of soaked seeds of the same kind + into another vessel with a saturated bedding of the same material. + In a third vessel place the same number of soaked seed, covering + them partially with water, and in a fourth cover the same number + entirely. Label them 1, 2, 3, and 4; keep all together in a warm, + even temperature, and observe at intervals of twenty-four hours for + a week. What condition as to moisture do you find most favorable + to germination? Would seeds germinate in the entire absence of + moisture? How do you know? + + EXPERIMENT 27. WAS IT THE PRESENCE OF TOO MUCH WATER, OR THE LACK + OF AIR CAUSED BY IT, THAT INTERFERED WITH GERMINATION IN THE LAST + EXPERIMENT?—To answer this question experimentally is not easy, + since it is difficult to obtain a complete vacuum without special + appliances. The simplest way is to fill with mercury a glass tube + 30 inches long, closed at one end, and invert it over a small + vessel—a teacup, or an egg cup will answer—containing mercury + enough to cover the bottom to a depth of two or three centimeters + (see Appendix, Weights and Measures, for English equivalents.) + The tube must be supported in such a way that its lower end will + dip into the mercury without touching the bottom of the vessel. + With a pair of forceps insert under the mouth of the tube two or + three seeds that have been well soaked in water deprived of air + by previous boiling. Being lighter than mercury, they will float + to the top, where there is a complete absence of air while other + conditions favorable to germination are present. Before releasing, + they should be well shaken under the mercury to free them from air + bubbles, and if the coats are loose fitting so that they can be + removed without injury to the parts inclosed in them, they should + be slipped off in order to get rid of any imprisoned air they + may contain. Additional moisture may be supplied, if necessary, + by injecting, by means of a medicine dropper inserted under the + mouth of the tube, a drop or two of water that has been previously + boiled. Keep in a warm, even temperature, under conditions + favorable to germination, and compare the behavior of the seeds + with those placed in the different vessels in Exp. 26. + + If appliances for this experiment are lacking, a rough + approximation can be made by using the seeds of aquatic plants, + such as the lotus, water lily, and the so-called Chinese sacred + bean, sold in the variety stores, which we know are capable of + germinating in the limited amount of air contained in ordinary + soil water. Place an equal number of such seeds, of about the same + size and weight, on a bedding of common garden soil in two glass + tumblers. Fill one vessel a little over half full of ordinary soil + water and the other to the same height with water from which the + air has been expelled by boiling. Pour over the liquid a film of + sweet oil or castor oil, to prevent the access of air, leaving the + surface of the water in the other vessel exposed. In which do the + seeds come up most freely? + +[Illustration: FIG. 47.—To find out the proper depth at which to +plant seeds.] + + Some seeds, especially those rich in proteins, as peas and beans, + will germinate in a vacuum, because oxygen is supplied for a time + by the chemical decomposition of substances in their tissues which + contain it, but when these are exhausted, respiration ceases and + death ensues. + + EXPERIMENT 28. DOES THE DEPTH AT WHICH SEEDS ARE PLANTED AFFECT + THEIR GERMINATION?—Plant a number of peas or grains of corn at + different depths in a wide-mouthed glass jar filled with moist + sand, as shown in Fig. 47, the lowest ones at the bottom, the top + ones barely covered. Try different kinds of seed and grain,—radish, + squash, cotton, or wheat,—and watch them make their way to the + surface. Do you notice any difference in this respect between large + seed and small ones? Between those with thick cotyledons and thin + ones? At what depth do you find, from your recorded observations, + that seed germinate best? + + EXPERIMENT 29. WHAT TEMPERATURE IS MOST FAVORABLE TO + GERMINATION?—Put half a dozen soaked beans on moist cotton or + sawdust in three wide-mouthed bottles of the same size or in + germinators arranged as in Figs. 48, 49, the seed also being + selected with a view to similarity of size and weight. Keep one at + a freezing temperature; the second in a temperature of 15° to 20° + C. (see Appendix for Fahrenheit equivalents); and the third, at + 30° C. If a place can be found near a stove or a register, where + an even temperature of about 125° F. is maintained, place a fourth + receptacle there. Observe at intervals of twenty-four hours for a + week or ten days, keeping the temperature as even as possible, and + maintaining an equal quantity of moisture in each vessel. Make a + daily record of your observations. What temperature do you find + most favorable to germination? + +[Illustration: FIGS. 48, 49.—Home-made germinators: 48, closed; 49, +showing interior arrangement.] + + EXPERIMENT 30. AT WHAT TEMPERATURE DO SEEDS LOSE THEIR + VITALITY?—Place about two dozen each of grains of corn, beans, + squash seed, and castor beans, with an equal number of plum or + cherry stones, in water, and heat to a temperature of 150° F. After + an exposure of ten minutes, take out six of each kind and place + in germinators made of two plates with moist sand or damp cloth + between them, as shown in Figs. 48, 49. Raise the temperature to + 175° F., and after ten minutes take out six more of each kind of + seed and place in another germinator. Raise the water in the vessel + to 200°, take out another batch of seeds; raise to the boiling + point for ten minutes more, and plant the remaining six of each + lot. Number the four germinators, and observe at intervals of + twenty-four hours for two weeks. The harder kinds should be kept + under observation for three or four weeks, as they germinate slowly. + + Try the same experiments with the same kinds of seeds at a dry + heat, using a double boiler to prevent scorching, and record + observations as before. + + EXPERIMENT 31. TIME REQUIRED FOR GERMINATION.—Arrange in + germinators seeds of various kinds, such as corn, wheat, peas, + turnip, apple, orange, grape, castor bean, etc. “Clip” some of the + harder ones and keep all the kinds experimented with under similar + conditions as to moisture, temperature, etc., and record the time + required for each to sprout. What is the effect of clipping, and + why? + + EXPERIMENT 32. ARE VERY YOUNG OR IMMATURE SEEDS CAPABLE OF + GERMINATING?—Plant some seeds from half-grown tomatoes, and grains + of wheat, oats, or barley before they are ready for harvesting. Try + as many kinds as you like, and see how many will come up. Notice + whether there is any difference in the health and vigor of plants + raised from seeds in different stages of maturity. + + EXPERIMENT 33. THE RELATIVE VALUE OF PERFECT AND INFERIOR + SEED.—From a number of seeds of the same species select half a + dozen of the largest, heaviest, and most perfect, and an equal + number of small, inferior ones. If a pair of scales is at hand, the + different sets should be weighed and a record kept for comparison + with the seedlings at the end of the experiment. Plant the two sets + in pots containing exactly the same kind of soil, and keep under + identical conditions as to light, temperature, and moisture. Keep + the seedlings under observation for two or three weeks, making + daily notes and occasional drawings of the height and size of the + stems, and the number of leaves produced by each. + +[Illustration: FIGS. 50, 51.—Stem development of seedlings: 50, +raised from healthy grains of barley; weight, 39.5 grams (about 500 +grs.); 51, raised under exactly similar conditions from the same +number of inferior grains; weight, 23 grams (about 350 grs.).] + +[Illustration: FIGS. 52, 53.—Improvement of corn by selection: 52, +original type; 53, improved type developed from it.] + +=33. Resistance to heat and cold.=—In making experiments with regard +to temperature, notice how the extremes tolerated are influenced, +first, by the length of time the seeds are exposed; second, by the +amount of water contained in them; and third, by the nature of the +seed coats. Every farmer knows that the effect of freezing is much +more injurious to plants or parts of plants when full of sap (water) +than when dry. This, in the opinion of the most recent investigators, +is because the water in the spaces outside the cells freezes first +and as moisture is gradually withdrawn from the inside to take its +place, the soluble salts which may be present in the cell sap become +more concentrated, and by their chemical action on the contained +proteins cause them to be precipitated, or “salted out,” as we see +sugar or salt precipitated from solutions of those substances when +water is withdrawn by evaporation. In this way, it is believed, the +fundamental protoplasm of the cell may be so disorganized that death +ensues if the freezing is continued long enough, since the protein +precipitates become “denatured” and cannot be reabsorbed if kept +in a solid state too long. The length of time necessary to produce +death from this cause is, of course, different in different plants, +according to the kind of salts dissolved in the sap and the nature of +the proteins acted on by them. The proteins in the sap of Begonia, +or Pelargonium, plants which are very sensitive to cold, yield a +denatured precipitate at, or a little below the freezing point of +water, while those of winter rye withstand a temperature of -15° C., +and of pine needles, -40° C. + +Mechanical injury through rupture of parts by freezing is not apt +to cause serious damage except in cases of sudden and violent cold +at a time when the tissues are gorged with sap, as not infrequently +happens during the abrupt changes of temperature which sometimes +occur in spring after the trees have put forth their leaves. In an +extreme case of this kind, the writer has seen the trunk of an oak +a foot or more in diameter split in deep seams from the effects of +freezing. + +=34. The length of time during which seeds may retain their +vitality.=—No direct experiment can be made to test this point, +since it would require months, or even years, covering in some +instances more than the lifetime of a generation. It has been stated +on good authority that seeds of the water chinquapin (Nelumbo) have +germinated after more than a hundred years, and moss spores preserved +in herbariums, after fifty. But the records in such cases are not +always trustworthy, and there is absolutely no foundation for the +statements sometimes made about the germination of wheat grains found +preserved with mummies over two thousand years old. If kept perfectly +dry, however, seed may sometimes be preserved for months, or even +years. Peas have been known to sprout after ten years, red clover +after twelve, and tobacco after twenty. Ordinarily, however, the +vitality of seeds diminishes with age, and in making experiments it +is best to select fresh ones. Those used for comparison should also, +as far as possible, be of the same size and weight. + +=35. Effect of precocious germination.=—It has been found by +experiment that plants raised from immature seed, when they will +germinate at all (Exp. 32), yield earlier and larger crops than the +same kinds from mature seed. Early tomatoes and some other vegetables +are produced in this way. The majority of seeds, however, require +a period of rest before beginning their life work. Those that are +forced to take up the burden of “child labor” show the effect of such +abnormal condition by yielding fruits that are smaller and less firm +than those raised from mature seed, so that they do not keep well and +have to be marketed quickly. Under what circumstances does it pay to +cultivate such fruits? + + + Practical Questions + + 1. What are the principal external conditions that affect + germination? (Exps. 26-29.) + + 2. What effect has cold? want of air? too much water? + + 3. Is light necessary to germination? + + 4. What is the use of clipping seeds? (Exps. 12, 13, 14, and + Material, p. 12.) + + 5. In what cases should it be resorted to? (Exp. 31.) + + 6. Why will seed not germinate in hard, sunbaked land without + abundant tillage? Why not on undrained or badly drained land? + (Exps. 26, 27.) + + 7. Will seeds that have lost their vitality swell when soaked? + (Exp. 16.) + + 8. Are there any grounds for the statement that the seeds of plums + boiled into jam have sometimes been known to germinate?[1] (33; + Exp. 30.) + + 9. Could such a thing happen in the case of apple or sunflower + seed, and why or why not? (33.) + + 10. Does it make any difference in the health and vigor of a plant + whether it is grown from a large and well-developed seed or from a + weak and puny one? (Exp. 33.) + + 11. Would a farmer be wise who should market all his best grain and + keep only the inferior for seed? + + 12. What would be the result of repeated plantings from the worst + seed? + + 13. Of constantly replanting the best and most vigorous? + + 14. Suppose seed would germinate without moisture; would this be an + advantage, or a disadvantage to agriculturists? + + 15. Why is a cool, dry place best for keeping seeds? (Exps. 26, 29.) + + 16. Why are the earliest tomatoes found in the market usually + smaller than those offered later? (35.) + + 17. Why is continued rain so injurious to wheat, oats, and other + grains before they are mature enough to be harvested? (35; Exp. 32.) + + 18. Would the same effect be likely to occur in the case of very + oily seeds, such as flax and castor beans? Why? (Suggestion: try + the effect of putting water on a piece of oiled paper.) + + 19. Explain why many seeds cannot germinate successfully without + air. (30, 31; Exp. 25.) + + 20. Mention some of the practical advantages that a farmer, a + gardener, or a careful housewife might gain from experiments like + those made in this section. + + 21. Explain why seeds can endure so much greater extremes of + temperature than growing plants. (23, 33.) + + + III. DEVELOPMENT OF THE SEEDLING + + MATERIAL.—Seedlings of various kinds in different stages of growth. + It is recommended that the same species be used that were studied + in Section III, Chapter I, or such equivalents as may have been + substituted for them. Enough should be provided to give each pupil + three or four specimens in different stages of development. Seeds, + even of the same kind, develop at such different rates that it + will probably not be necessary to make more than two plantings of + each sort, from 2 to 5 days apart. Soaked seeds of corn and wheat + will germinate in from 3 to 7 days, according to the temperature; + oats in 1 to 4; beans in 4 to 6; squash and castor beans in from + 8 to 10. Very obdurate ones may be hastened by clipping. Keep the + germinators in an even temperature, at about 70° to 80° F. + + Pine is a very difficult seed to germinate, requiring usually + from 18 to 21 days. By soaking the mast for twenty-four hours and + planting in damp sand or sawdust kept at an even temperature of 23° + C. or about 75° F., specimens may be obtained. + +[Illustration: FIGS. 54, 55.—Seedling of corn (_after_ GRAY): 54, +early stage of germination; 55, later stage.] + +=36. Seedlings of monocotyls.=—Examine a seedling of corn that has +just begun to sprout; from which side does the seedling spring, the +plain or the grooved one? Refer to your sketch of the dry grain and +see if this agrees with the position of the embryo as observed in the +seed. Make sketches of four or five seedlings in different stages of +advancement, until you reach one with a well-developed blade. From +what part of the embryo has each part of the seedling developed? +Which part first appeared above ground? Is it straight, or bent in +any way? In what direction does the plumule grow? The hypocotyl? Does +the cotyledon appear above ground at all? Slip off the husk and see +if there is any difference in the size and appearance of the contents +as you proceed from the younger to the older plants. How would you +account for the difference? + +=37. The root.=—Examine the lower end of the hypocotyl and find where +the roots originate; would you say that they are an outgrowth from +the stem, or the stem from the root? Observe that the root of the +corn does not continue to grow in a single main axis like that of +the castor bean, but that numerous adventitious and secondary roots +spring from various points near the base of the hypocotyl and spread +out in every direction, thus giving rise to the fibrous roots of +grains and grasses. + +=38. Root hairs.=—Notice the grains of sand or sawdust that cling to +the rootlets of plants grown in a bedding of that kind. Examine with +a lens and see if you can account for their presence. Lay the root +in water on a bit of glass, hold up to the light and look for root +hairs; on what part are they most abundant? + +[Illustration: FIG. 56.—Seedling of wheat, with root hairs.] + +The hairs are the chief agents in absorbing moisture from the +soil. They do not last very long, but are constantly dying and +being renewed in the younger and tenderer parts of the root. These +are usually broken away in tearing the roots from the soil, so +that it is not easy to detect the hairs except in seedlings, even +with a microscope. In oat, maple, and radish seedlings they are +very abundant and clearly visible to the naked eye. The amount of +absorbing surface on a root is greatly increased by their presence. + +[Illustration: FIG. 57.—Diagrammatic section of a root tip: _a_, +cortex; _b_, central cylinder in which the conducting vessels are +situated; _c_, root cap; _g_, growing point.] + +=39. The root cap.=—Look at the tip of the root through your lens +and notice the soft, transparent crescent or horseshoe-shaped mass +in which it terminates. This is the root cap and serves to protect +the tender parts behind it as the roots burrow their way through the +soil. Being soft and yielding, it is not so likely to be injured by +the hard substances with which it comes in contact as would be the +more compact tissue of the roots. It is composed of loose cells out +of which the solid root substance is being formed; the growing point +of the root, _g_, is at the extremity of the tip just behind the +cap, _c_ (Fig. 57). The cap is very apparent in a seedling of corn, +and can easily be seen with the naked eye, especially if a thin +longitudinal section is made. It is also well seen in the water roots +of the common duckweed (_Lemna_), and on those developed by a cutting +of the wandering Jew, when placed in water. Are there any hairs on +the root cap? Can you account for their absence? + + NOTE.—For a minute study of the structure of roots, see =67=. + +=40. Organs of vegetation.=—The three parts, root, stem, and leaf, +are called organs of vegetation in contradistinction to the flower +and fruit, which constitute the organs of reproduction. The former +serve to maintain the plant’s individual existence, the latter to +produce seed for the propagation of the species, so we find that the +seed is both the beginning and the end of vegetable life. + +[Illustration: FIG. 58.—Seedlings of bean in different stages +of growth: _cc_, cotyledons, showing the plumule and hypocotyl +before germination; _a_, _b_, _d_, and _e_, successive stages of +advancement. At _d_ the arch of the hypocotyl is beginning to +straighten; at _e_ it has entirely erected itself.] + +=41. Definitions.=—Organ is a general name for any part of a living +thing, whether animal or vegetable, set apart to do a certain work, +as the heart for pumping blood, or the stem and leaves of a plant for +conveying and digesting sap. By “function” is meant the particular +work or office that an organ has to perform. + +=42. Seedlings of dicotyls. The bean.=—Sketch, without removing it, a +bean seedling that has just begun to show itself above ground; what +part is it that protrudes first? Sketch in succession four or five +others in different stages of advancement. Notice how the hypocotyl +is arched where it breaks through the soil. Does this occur in the +monocotyls examined? Do the cotyledons of the bean appear above +ground? How do they get out? Can you perceive any advantage in their +being dragged out of the ground backwards in this way rather than +pushed up tip foremost? What changes have the cotyledons undergone +in the successive seedlings? Remove from the earth a seedling just +beginning to sprout and sketch it. From what point does the hypocotyl +protrude through the coats? Does this agree with its position as +sketched in your study of the seed? In which part of the embryo does +the first growth take place? + +Remove in succession the several seedlings you have sketched and +note their changes. How does the root differ from that of the corn +and oats? The first root formed by the extension of the hypocotyl is +the _primary_ root and should be so labeled in your drawings; the +branches that spring from it are _secondary_ roots. Look for root +hairs; if there are any, where do they occur? + +[Illustration: FIG. 59.—Stages in the germination of a typical +seedling of the squash family: _a_, a seed before germination; _b_, +_c_, _e_, the same in different stages of growth; _d_, the empty +testa, with kernel removed; _hi_, hilum; _m_, micropyle; _p_, _p_, +the peg in the heel; _h_, _h_, _h_, the hypocotyl; _ar_, arch of the +hypocotyl; _co_, cotyledons; _pl_, plumule; _pr_, primary root; _sc_, +secondary roots.] + +=43. Germination of the squash.=—How does the manner of breaking +through the soil compare with that of the bean? With the corn? +From which end of the seed, the large or the small one, does the +hypocotyl spring? Do the cotyledons come above ground? How do they +get out of the seed coat? Notice the thick protuberance developed +by the hypocotyl and pressing against the lower half of the coat at +the point where the hypocotyl breaks through. This is called the +“peg”; can you tell its use? Could the cotyledons get out of their +hard covering without it? Slip the peg below the coat in one of your +growing specimens, leave it in the soil, and see what will happen. +How do the cotyledons of the squash differ from those of the bean +as they come out of the seed cover? Do they act as foliage leaves? +Do you see any difference in the development of the plumule in the +two seeds (Figs. 19, 25) to account for the different behavior of +the cotyledons? Sketch three seedlings in different stages, labeling +correctly the parts observed. Make a similar study of the castor +bean, or other seedling selected by your teacher, and illustrate by +drawings. + +=44. Arched and straight hypocotyls.=—This difference in the manner +of getting above ground is an important one. That by means of the +arched hypocotyl is, in general, characteristic of the process of +germination in which the cotyledons come above ground, while the +straight kind, which was illustrated in the corn and wheat, is the +prevailing method when the cotyledons remain below ground. Can you +give a reason for the difference? + +[Illustration: FIG. 60.—Pine seedling (_After_ GRAY).] + +=45. Polycotyledons; germination of the pine.=—Examine a pine +seedling just beginning to sprout. What part emerges first from +the seed coat? Where does it break through? Where did you find the +micropyle in the pine seed? (15.) Can you give a reason why the +hypocotyl in seeds should break through the coats at this point? How +do the cotyledons get out of the testa? Is the hypocotyl arched or +straight in germination? How does it compare with the bean and squash +in this respect? With the corn? Is any endosperm left in the testa +after the cotyledons have come out? What has become of it? Do the +cotyledons function as leaves? How many of them have the specimen +you are studying? Notice the little knob or button at the upper +end of the hypocotyl, just above the point where the cotyledons are +attached; this is the _epicotyl_, or part above the cotyledons, here +identical with the plumule; does it develop as rapidly as in the +other seedlings you have examined? + +=46. Relation of parts in the seedling.=—Before leaving this subject, +it is important to fix clearly in mind the different parts of the +germinating seedling and their relation to both the embryo from +which they originated and the plant into which they are to develop. +The part labeled “hypocotyl” in your sketches is all that portion +of the embryo below the point of attachment of the cotyledons. In +germination its upper part will become the stem, and in the embryo +constitutes the _caulicle_, or stemlet, while its lower part, from +which the root will develop, is the _radicle_, or rootlet; hence +the term “hypocotyl” includes both the future root and stem. The +plumule is that part of the embryo between the cotyledons and _above_ +their point of attachment to the caulicle. It is the upward growing +point of the young plant, and hence the place of attachment of the +cotyledon is the first _node_, or point of leaf origin, on the stem. + +The epicotyl, in contradistinction to the hypocotyl, is all that +part of the plant _above_ the insertion of the cotyledons. Before +germination it is identical with the plumule. As the seedling grows, +the epicotyl advances its growing point by adding new nodes and +_internodes_, as the spaces between the successive points of leaf +insertion are called. + +=47. Botanical terms.=—As the prefixes _hypo_ and _epi_ are of +frequent occurrence in botanical works, it will aid in understanding +their various compounds if you will remember that _hypo_ always +refers to something below or beneath, and _epi_, to something over +or above. With this idea in mind you will see that botanical terms +are a labor-saving device, since it is much easier, in making notes, +to use a single descriptive word than to write out the long English +equivalent, such as “the part under (or over) the cotyledons.” + + + Practical Questions + + 1. Do the cotyledons, as a general thing, resemble the mature + leaves of the same plants? + + 2. Name some plants in which you have observed differences, and + account for them; could convenience of packing in the seed coats, + for instance, or of getting out of them, have any bearing on the + matter? + + 3. Does the position in which seeds are planted in the ground have + anything to do with the position of the seedlings as they appear + above the surface? + + 4. Is this fact of any importance to the farmer? + + 5. Will grain that has begun to germinate make good meal or flour? + Why? (27, 36; Exp. 25.) + + + IV. GROWTH + + MATERIAL.—Two young potted plants; some lily or hyacinth + bulbs; seedlings of different kinds,—some with well-developed + taproots,—apple, cotton, and maple are good examples. + + APPLIANCES.—A small flat dish, some mercury, and a piece of cork. + +[Illustration: FIGS. 61, 62.—Seedling of corn, marked to show +region of growth: 61, early stage of germination; 62, later stage.] + + EXPERIMENT 34. HOW DOES THE ROOT INCREASE IN LENGTH?—Mark off the + root of a very young corn seedling into sections by moistening + a piece of sewing thread with indelible ink and applying it to + the surface of the root at intervals of about two millimeters (⅒ + of an inch), or by tying a thread lightly around it at the same + intervals. Lay the seedling on a moist bedding between two panes + of glass kept apart by a sliver of wood to prevent their injuring + the root by pressure. Watch for a day or two, and you will see that + growth takes place from a point just back of the tip (Figs. 61, 62). + + Mark off a seedling of the bean in the same way and watch to see + whether it increases in the same manner as the corn. + + EXPERIMENT 35. HOW DOES THE STEM INCREASE IN LENGTH?—Mark off a + portion of the stem of a bean seedling as explained in the last + experiment, and find out how it grows. Allow a seedling to develop + until it has put forth several leaves and measure daily the spaces + between them. Label these spaces in your drawings, “internodes,” + and the points where the leaves are attached, “nodes.” Does an + internode stop growing when the one next above it has formed? When + is growth most rapid? Reverse the position of a number of seedlings + that have just begun to sprout and watch what will happen. After a + few days reverse again and note the effect. + +[Illustration: FIGS. 63, 64.—Root of bean seedling, measured to show +region of growth: 63, early stage of germination; 64, later stage. +FIGS. 65, 66.—Stem of bean seedling, measured to show region of +growth: 65, early stage of growth; 66, later stage.] + + EXPERIMENT 36. CAN PLANTS GROW AND LOSE WEIGHT AT THE SAME + TIME?—Remove the scales from a white lily bulb, weigh them, and + lay in a warm, but not too damp place, away from the light. After + a time bulblets will form at the bases of the scales. Weigh + them again, and if there has been any loss, account for it. The + experiment may be tried by allowing a potato tuber or a hyacinth + bulb to germinate without absorbing moisture enough to affect its + weight. + +[Illustration: FIGS. 67, 68.—Experiment showing the direction of +growth in stems: 67, young potato planted in an inverted position; +68, the same after an interval of eight days.] + + EXPERIMENT 37. IS THE DIRECTION OF GROWTH A MATTER OF ANY + IMPORTANCE?—Plant in a pot suspended as shown in Fig. 67, a healthy + seedling of some kind, two or three inches high, so that the + plumule shall point downward through the drain hole and the root + upward into the soil. Watch the action of the stem for six or + eight days, and sketch it at successive intervals. After the stem + has directed itself well upward, invert the pot again, and watch + the growth. After a week remove the plant and notice the direction + of the root. Sketch it entire, showing the changes in direction of + growth. + + At the same time that this experiment is arranged, lay another pot + with a rapidly growing plant on one side, and every forty-eight + hours reverse the position of the pot, laying it on the opposite + side. At the end of ten or twelve days remove the plant and + examine. How has the growth of root and stem been affected? + + What do we learn from these experiments and from Exp. 35 as to the + normal direction of growth in these two organs respectively? Can + you think of any natural force that might influence this direction? + +[Illustration: FIG. 69.—Experiment showing the root of a seedling +forcing its way downward through mercury.] + + EXPERIMENT 38. TO SHOW THAT PLANTS WILL EXERT FORCE RATHER THAN + CHANGE THEIR DIRECTION OF GROWTH.—Pin a sprouted bean to a cork and + fasten the cork to the side of a flat dish, as shown in Fig. 69. + Cover the bottom of the dish with mercury at least half an inch + deep, and over the mercury pour a layer of water. Cover the whole + with a pane of glass to keep the moisture in, and leave for several + days. The root will force its way downward into the mercury, + although the latter is fourteen times heavier than an equal bulk + of the bean root substance, and the root must thus overcome a + resistance equal to at least fourteen times its own weight. + +=48. What growth is.=—With the seedling begins the growth of the +plant. Most people understand by this word mere increase in size; but +growth is something more than this. It involves a change of form, +usually, but not necessarily, accompanied by increase in bulk. Mere +mechanical change is not growth, as when we bend or stretch an organ +by force, though if it can be kept in the altered position till such +position becomes permanent, or as we say in common speech, “till it +grows that way,” the change may become growth. To constitute true +growth, the change of form must be permanent, and brought about, or +maintained, by forces within the plant itself. + +=49. Conditions of growth.=—The internal conditions depend upon +the organization of the plant. The essential external conditions +are the same as those required for germination: food material, +water, oxygen, and a sufficient degree of warmth. It may be greatly +influenced by other circumstances, such as light, gravitation, +pressure, and (probably) electricity; but the four first named are +the essential conditions without which no growth is possible. + +=50. Cycle of growth.=—When an organ becomes rigid and its +form fixed, there is no further growth, but only nutrition and +repair,—processes which must not be confounded with it. Every plant +and part of a plant has its period of beginning, maximum, decline, +and cessation of growth. The cycle may extend over a few hours, as in +some of the fungi, or, in the case of large trees, over thousands of +years. + +=51. Geotropism.=—The general tendency of the growing axes of +plants to take an upward and downward course as shown in Exp. +37—in other words, to point to and from the center of the earth—is +called _geotropism_. It is _positive_ when the growing organs point +downward, as most primary roots do; _negative_ when they point +upward, as in most primary stems; and _transverse_, or _lateral_, +when they extend horizontally, as is the case with most secondary +roots and branches. + +=52. Gravity and growth.=—It cannot be proved directly that +geotropism is due to gravity, because it is not possible to remove +plants from its influence so as to see how they would behave in +its absence. The effect of gravity may be neutralized, however, by +arranging a number of sprouting seeds on the vertical disk of a +clinostat, an instrument fitted with a clockwork movement by means of +which they may be kept revolving steadily for several days. By this +constant change of position gravity is made to act on them in all +directions alike, which is the same in some respects as if it did not +act at all. If the disk is made to revolve rapidly, the growing root +tips turn toward the axis of motion, without showing a tendency to +grow downward. We may then conclude that geotropism is a reaction to +gravity. + +=53. Geotropism an active force.=—It must be noted, however, that the +force here alluded to is not the mere mechanical effect of gravity, +due to weight of parts, as when the bough of a fruit tree is bent +under the load of its crop, but a certain stimulus to which the plant +reacts by a spontaneous adjustment of its growing parts. In other +words, geotropism is an active, not a passive function, and the plant +will overcome considerable resistance in response to it. (Exp. 38). + +=54. Other factors.=—The direction of growth is influenced by many +other factors, such as light, heat, moisture, contact with other +bodies, and perhaps by electricity. The result of all these forces is +an endless variety in the forms and growth of organs that seems to +defy all law. + +[Illustration: FIG. 70.—A piece of a haulm of millet that has been +laid horizontally, righting itself through the influence of negative +geotropism.] + +Heat, unless excessive, generally stimulates growth; contact +sometimes stimulates it, causing the stem to curve away from the +disturbing object, and sometimes retards it, causing the stem to +curve toward the object of contact by growing more rapidly on the +opposite side, as in the stems of twining vines. Light stimulates +nutrition, but generally retards growth. The movements of plants +toward the light are effected in this way; growth being checked on +that side, the plant bends toward the light. + + + Practical Questions + + 1. Why do stems of corn, wheat, rye, etc., straighten themselves + after being prostrated by the wind? (51, 54.) + + 2. Do plants grow more rapidly in the daytime, or at night? (54.) + + 3. Reconcile this with the fact that green plants will die if + deprived of light. + + 4. Which grows more rapidly, a young shoot or an old one? (31, 50.) + + 5. Which, as a general thing, are the more rapid growers, annuals + or perennials? Herbaceous or woody-stemmed plants? + + 6. Name some of the most rapid growers you know. + + 7. Of what advantage is this habit to them? + + 8. Why do roots form only on the under side of subterraneous stems? + (51.) + + 9. Why do new twigs develop most freely on the upper side of + horizontal branches? (51.) + + + Field Work + + (1) Notice the various seedlings met with in your walks and see how + many you can recognize by their resemblance to the mature plants. + Account for any differences you may observe between seedlings + and older plants of the same species. Observe the cotyledons as + they come up and their manner of getting out of the ground, and + notice the ways in which this is influenced by moisture, light, + and the nature of the soil. Where the cotyledons do not appear, + dig into the ground and find out the reason. Notice which method + of emergence occurs in each case, the arched, or straight, and + account for it. Observe particularly the behavior of seedlings in + hard, sunbaked soil. If you see any of them lifting cakes of earth, + compare the size and weight of the cake with that of the seed; if + there is any disparity, what does this imply? What is the force + called which the plant exercises in lifting the weight? (51.) + + (2) Notice if there are any seeds germinating successfully on top + of the ground, and find out by what means their roots get into the + soil. Observe what effect sun and shade, moisture and drought, and + the nature of the soil have on the process. Find out whether roots + exercise force in penetrating the soil; what kinds they penetrate + most readily, and what kinds, if any, they fail to penetrate at + all. Notice whether seedlings with taproots, like the turnip and + castor bean, or those with fibrous roots, like corn and wheat, are + more successful in working their way downward. + + (3) Look for tree seedlings. Explain why seedlings of fruit trees + are so much more widely distributed in cultivated districts, and so + much easier to find than those of forest trees. Where do the latter + occur, as a general thing? Account for the fact that seedling + trees are so much more rare than germinating herbs, and why trees + like the oak and chestnut and black walnut propagate so much more + slowly, in a state of nature, than the pine, cedar, ash, and maple. + + (4) Observe the direction of growth in plants on the sides of + gullies and ravines, and tell how it is influenced by geotropism. + Notice whether there are other influences at work; for instance, + light, or in the case of roots, the attraction of moisture. + + + + +CHAPTER III. THE ROOT + + + I. OSMOSIS AND THE ACTION OF THE CELL + + MATERIAL.—For experiments in osmosis provide fresh and boiled + slices of red beet, a fresh egg, a piece of ox bladder or some + parchment paper; glass tubing, thread, twine, elastic bands, salt + and sugar solutions. A common medicine dropper with the small end + cut off will answer instead of tubing for making an artificial + cell; or an eggshell may be used, by blowing out the contents + through a puncture in the small end, and carefully chipping away a + portion of the shell at the big end, leaving the lining membrane + intact. The different liquids can be put into the shell and the + exposed membrane placed in contact with the liquid in the glass, + by fitting over the latter a piece of cardboard with a hole in + the center large enough for the exposed surface to protrude + sufficiently to touch the water. + +[Illustration: FIG. 71.—Artificial cell.] + +=55. Object of the experiments.=—In order to understand clearly the +action of roots in absorbing nutrients from the soil, it will be +necessary to learn something about the movement of liquids through +the cells, upon which the physiological processes of the plant +depend. For this purpose make an artificial cell by tying a piece of +ox bladder or parchment paper tightly over one end of a small glass +tube, as shown in Fig. 71. + + EXPERIMENT 39. HOW DOES ABSORPTION TAKE PLACE IN THE CELL?—(_a_) + Put some salt water in a wineglass, partly fill the tube of the + artificial cell with fresh water, and mark on the outside of both + vessels the height at which the contained liquid stands. Set the + tube in the glass of salt water and wait for results, having first + tested carefully to make sure that there are no leaks in the + membrane. After half an hour, notice whether there is any increase + of water in the glass, as indicated by the mark. If so, where did + it come from? Is there any loss of water in the tube? What has + become of it? How did it get out? Taste it to see if any of the + salt water has got in. Which is the heavier, salt water, or fresh? + (If you do not know, weigh an equal quantity of each.) In which + direction did the principal flow take place; from the heavier to + the lighter, or from the lighter to the heavier liquid? + + (_b_) Put a sugar or salt solution in the tube, and clear, fresh + water in the glass, marking the height in each as before. Does the + liquid rise or fall in the tube? Does any of it escape into the + water of the glass, and if so, is it more or less than before? + Which now contains the denser fluid, the tube or the glass? What + principle governs the course of the liquid? Try the same experiment + with (_c_), the same liquid in both vessels, and notice whether + there is a greater flow in one direction than the other, as + indicated by a comparison with the marks on the outside. (_d_) Put + in the tube some of the white of a raw egg, insert in a glass of + pure water, and note the effect. (_e_) Reverse, with water in the + tube and white of egg in the glass. Does the water rise in the tube + as before? Test the contents for proteins; has any of the albumin + passed through the membrane into the tube? + + EXPERIMENT 40. TO TEST THE BEHAVIOR OF LIVING AND DEAD CELLS.—Slice + a fresh piece of red beet into a vessel of water and of a boiled + one into another vessel of the same liquid at the same temperature. + What difference do you notice? Can you think of any reason why the + boiled one gives up its juices and the other one does not? + +=56. Osmosis.=—The passage of liquids or of solids in solution +through membranes is known as _osmosis_. Our experiments have +shown that the principles governing the osmotic movement are: (1) +the passage of water from the thinner liquid toward the denser +takes place more rapidly than in the opposite direction; (2) the +rapidity of the transfer depends on the difference in density; (3) +crystallizable substances in solution, like sugar and salt, osmose +readily; (4) albuminous or gelatinous substances, such as the white +of an egg, osmose so slowly that the cell wall may be regarded as +practically impermeable to them. + +=57. Osmosis a form of diffusion.=—Osmosis is related to diffusion +as a part to the whole. In other words, it is a name given to the +process when it takes place through a membrane, whether solid, as the +outer wall of the cell, or semi-fluid, as the inner wall of living +protoplasm. Diffusion may therefore take place without osmosis, +that is, in the absence of a membrane, as, for example, when we +sweeten our tea or coffee by allowing sugar to diffuse through it. +Many membranes offer little resistance to the osmotic movement of +crystallizable substances. Such membranes are said to be _permeable_. +Membranes which are not permeable to the dissolved solids, are called +_semi-permeable_, since they allow the diffusion of water but not of +the substances in solution. Living protoplasm is of this class. It is +only very slightly permeable to many substances toward which, when +dead, it acts as a permeable membrane. + +=58. Absorption in living and dead cells.=—There is one great +difference between the action of the artificial cell used in the +foregoing experiments and that of the cells of which a living body +is built up. The living cell always has at least two membranes. One +of these, the cell wall, is readily permeable, while the other, the +protoplasm, is semi-permeable—that is, substances in solution usually +diffuse more or less slowly, while water diffuses rapidly. Hence +in the living cell the protoplasm exercises a power of absorption +independent of the cell wall, sometimes rejecting substances admitted +by the latter, sometimes retaining others to which it is permeable, +as shown in Exp. 40. In the boiled beet the protoplasm had been +killed and the red coloring matter passed through it unhindered, +while in the living one it was held back by the protoplasmic lining, +which is thus seen to control the absorptive properties of the cell. + +=59. Plasmolysis.=—Cells can be killed or injured in other ways +than by heat; for example, by cold, by poisons, by starvation, and +by overfeeding through the use of too much fertilizer or too rich +a one. In this last case, the soil water becomes impregnated with +soluble matter from the manure, which may render it denser than the +sap in the roots. When this happens, it will cause the osmotic flow +to set outward and thus deplete the cell of its water; whence we have +the paradox that a cell, or even a whole plant, may be starved by +overfeeding. This action of osmosis in withdrawing the contents from +a cell is termed _plasmolysis_, and you can easily understand how +very important a knowledge of the principles governing it is to the +farmer in determining the application of fertilizers to his crops. + +Dead cells, although powerless to carry on the life processes of a +plant, have nevertheless important uses in serving the purposes of +mechanical support and also to some extent in assisting in the work +of absorption, though their function here is a purely mechanical one. + +[Illustration: FIG. 72.—Root of a tree enveloping a rock. The large +sycamore, whose base is partly concealed by the trumpet creeper on +the left of the picture, is growing in very hard, stony soil, and +one of its main roots has molded itself so completely to the ledge +of rock protruding on the right, that when a portion of it was torn +away, as shown where the light streak ends at _a_, the impress of its +fibers was so strongly marked on the rock as to give the latter the +appearance of a petrified root.] + +=60. Selective absorption.=—Different plants through their roots +absorb different substances from the soil water, or the same +substance in varying degrees. Hence, one kind of crop will exhaust +the soil of certain minerals while leaving other kinds intact, or +very little diminished; and _vice versa_, another kind will take +up abundantly what its predecessor has rejected. In this sense, +plants are said to exercise a selective power in the absorption +of nutrients. The expression must not be understood, however, as +implying any kind of volitional discrimination. It is merely a short +and convenient way of saying that the cells of different plants +possess different degrees of permeability to certain substances, some +being more permeable to one thing, some to another. But beyond this +rejection of untransmissible substances there is no active power of +discrimination, any substance that can pass through the cell wall and +its protoplasmic lining being taken in, whether useful, unnecessary, +or even harmful. These may, however, be got rid of by excretion, as +the superfluous water taken in with dissolved minerals is exhaled +from the leaves; or if incapable of passing out by osmosis, rendered +harmless and retained in the form of the curious “crystalloids” +found in various parts of plants. But while the kind of selection +exercised by vegetable cells implies no power of choice, as a matter +of fact those substances most used by the plant in carrying on its +life processes are absorbed in much greater quantities than others, +being transferred to parts where growth or other changes in the plant +tissues are going on, and there used up in the work of nutrition, or +excreted in part as waste products. In either case their passage from +cell to cell will give rise to a continuous osmotic current in that +direction, and the absorption of new matter will go on in proportion +to the amounts used up. + +[Illustration: FIG. 73.—Roots of elm and sycamore contending for +possession of the soil on a rocky bluff on the Potomac.] + +=61. Definition.=—Tissue is a word used to denote any animal or +vegetable substance having a uniform structure organized to perform +a particular office or function. Thus, for instance, we have bony +tissue and muscular tissue in animals; that is, tissue made of bone +substance and muscle substance and doing the work of bone and muscle +respectively. Likewise in plants, we have strengthening tissue +made up of hard, thick-walled cells, serving mainly for purposes +of mechanical support, and vascular tissue, made up of conducting +vessels for conveying sap—and so on, for every separate function. + + + Practical Questions + + 1. Why do raspberries and strawberries have a flabby, wilted look + if sugar has been put on them too long before they are served? (7, + 56.) + + 2. Where has the juice gone? What caused it to go out of the + berries? (56, 59.) + + 3. Is a knowledge of the principles governing osmosis of any + practical use to the housekeeper? + + 4. Why cannot roots absorb water as freely in winter as in summer? + (Suggestion: which is the heavier, cold or warm water?) + + 5. Why does fertilizing too heavily sometimes injure a crop? (59.) + + 6. Do you see any apparent contradiction between the action + of plasmolysis and the selective power of protoplasm? Can you + reconcile it? + + 7. If a piece of beet that has been frozen is placed in water + it will behave just as the slice of boiled beet did in Exp. 40; + explain. (58, 59.) + + + II. MINERAL NUTRIMENTS ABSORBED BY PLANTS + + MATERIAL.—A dozen or two each of different kinds of seeds and + grains. A small portion from a growing shoot of a woody and a + herbaceous land plant, and of some kind of succulent water or marsh + plant, such as arrow grass (_Sagittaria_), water plantain, etc. + + APPLIANCES.—A pair of scales; a lamp, stove, or other means of + burning away the perishable parts of the specimens to be studied. + + EXPERIMENT 41.—DO THE TISSUES OF PLANTS CONTAIN MINERAL + MATTER?—Take about a dozen each of grains and seeds of different + kinds, weigh each kind separately, and then dry them at a high + temperature, but not high enough to scorch or burn them. After they + have become perfectly dry, weigh them again. What proportion of the + different seeds was water, as indicated by their loss of weight in + drying? + + Burn all the solid part that remains, and then weigh the ash. What + proportion of each kind of seed was of incombustible material? What + proportion of the solid material was destroyed by combustion? + + EXPERIMENT 42.—DO THEY CONTAIN DIFFERENT KINDS AND QUANTITIES OF + MINERALS?—Test in the same way the fresh, active parts of any kind + of ordinary land plant (sunflower, hollyhock, pea vines, etc.), and + of some kind of succulent water or marsh plant (Sagittaria, water + lily, fern). Do you notice any difference in the amount of water + given off and of solid matter left behind? In the character of the + ashes left? Have you observed in general any difference between the + ashes of different woods; as, for instance, hickory, pine, oak? + Compare with the residue left in Exp. 21; would you judge that the + residual substances are of the same composition? + +[Illustration: FIG. 74.—Water cultures of buckwheat, showing effect +of the lack of the different food elements: 1, with all the elements; +2, without potassium; 3, with soda instead of potash; 4, without +calcium; 5, without nitrates or ammonia salts.] + +=62. Essential constituents.=—The composition of the ash of any +particular plant will depend upon two things: the absorbent capacity +of the plant itself and the nature of the substances contained in the +soil in which it grows. But chemical analysis has shown that however +the ashes may vary, they always contain some proportion of the +following substances: potassium (potash), calcium (lime), magnesium, +phosphorus, and (in green plants) iron. These elements occur in all +plants, and if any one of them is absent, growth becomes abnormal if +not impossible. + +The part of the dried substances that was burned away after expelling +the water consists, in all plants, mainly of carbon, hydrogen, +oxygen, nitrogen, and sulphur, in varying proportions. These five +rank first in importance among the essential elements of vegetable +life, and without them the plant cell itself, the physiological unit +of vegetable structure, could not exist. They compose the greater +part of the substance of every plant, carbon alone usually forming +about one half the dry weight. Other substances may be present in +varying proportions, but the two groups named above are found in all +plants without exception, and so we may conclude that (with the +possible addition of chlorine) they form the indispensable elements +of plant food. Carbon, hydrogen, oxygen, nitrogen, sulphur, and +phosphorus compose the structure of which the plant is built. The +other four ingredients do not enter into the substance as component +parts, but aid in the chemical processes by which the life functions +of the plant are carried on, and are none the less essential elements +of its food. Figure 74 shows the difference between a plant grown in +a solution where all the food elements are present, and others in +which some of them are lacking. + +[Illustration: FIG. 75.—Roots of soy bean bearing tubercle-forming +bacteria.] + +=63. How plants obtain their food material.=—Plants obtain their +supply of the various mineral salts from solutions in the soil +water which they absorb through their roots. With a few doubtful +exceptions, they cannot assimilate their food unless it is in a +liquid or gaseous form. Of the gases, carbon dioxide, oxygen, and +hydrogen can be freely absorbed from the air, or from water with +various substances in solution, but most plants are so constituted +that they cannot absorb free nitrogen from the air; they can take it +only in the form of compounds from nitrates dissolved in the soil, +and hence the importance of ammonia and other nitrogenous compounds +in artificial fertilizers. Some of the pea family, however, bear +on their roots little tubers formed by minute organisms called +bacteria, which have the power of extracting nitrogen directly from +the free air mingled with the soil; and hence the soil in which these +tuber-bearing legumes decay is enriched with nitrogen in a form ready +for use. + + + Practical Questions + + 1. Could any normal plant grow in a soil from which nitrogen was + lacking? Potash? Lime? Phosphorus? (62.) + + 2. Could it live in an atmosphere devoid of oxygen? Nitrogen? + Carbon dioxide? (62.) + + 3. Why are cow peas or other legumes planted on worn-out soil to + renew it? (63.) + + 4. Is the same kind of fertilizer equally good for all kinds of + soil? For all kinds of plants? (60, 62.) + + 5. Why does too much watering interfere with the nourishment of + plants? (Exps. 26, 27.) + + 6. Are ashes fit for fertilizers after being leached for lye? (62.) + + 7. Why will plants die, or make very slow growth, in pots, unless + the soil is renewed occasionally? (60, 62.) + + + III. STRUCTURE OF THE ROOT + + MATERIAL.—Taproot of a young woody plant not over one or two years + old; apple and cherry shoots make good specimens. For showing root + hairs, seedlings of radish, turnip, or oat are good, also roots of + wandering Jew grown in water; for the rootcap, corn, sunflower, + squash. + +[Illustration: FIG. 76.—Cross section of a young taproot; _a_, _a_, +root hairs; _b_, epidermis; _c_, cortical layer; _d_, fibrovascular +cylinder. Note the absence of medullary rays during the first year of +growth.] + +=64. Gross anatomy of the root.=—Cut a cross section of any woody +taproot, about halfway between the tip and the ground level, +examine it with a lens, and sketch. Label the dark outer covering, +_epidermis_, the soft layer just within that, _cortex_, the hard, +woody axis that you find in the center, _vascular cylinder_, and +the fine silvery lines that radiate from the center to the cortex, +_medullary rays_ (in a very young root these will not appear). Cut +a section through a root that has stood in coloring fluid for about +three hours and note the parts colored by the fluid. What portion of +the root, would you judge from this, acts as a conductor of the water +absorbed from the ground? + +Make a longitudinal section passing through the central portion of +the root and extending an inch or two into the lower part of the +stem. Do you find any sharp line of division between them? Notice the +hard, woody axis that runs through the center. This is the vascular +cylinder and contains the conducting vessels, the cut ends of which +were shown in cross section in Fig. 76. + +[Illustration: FIG. 77.—Verti-section of branching root, showing the +branches, _n_, _n_, originating in the central axis, _f_, and passing +through the cortex, _r_, _r_.] + +=65. Distinctions between root and stem.=—Pull off a branch from +the stem and one from the root; which comes off the more easily? +Examine the points of attachment of the two and see why this is so. +This mode of branching from the central axis instead of from the +external layers, as in the stem, is one marked distinction between +the structure of the two organs. In stems, moreover, branches occur +normally above the points of leaf insertion at the nodes (46), while +in the root they tend to arrange themselves in straight vertical +rows. The shoots and cions that often originate from them are not +normal root branches, but outgrowths from irregular or _adventitious_ +buds, that may occur on any part of a plant. The root is not divided +into nodes like the stem, and never bears leaves. + +[Illustration: FIG. 78.—Root of a tree on the side of a gulley, +acting as stem.] + +=66. The active part of the root.=—It is only the newest and most +delicate parts of the root that produce hairs and are engaged in the +active work of absorption, the older parts acting mainly as carriers. +Hence, old roots lose much of their characteristic structure and +take on more and more of the office of the stem, until there is +practically no difference between them. On the sides of gullies, +where the earth has been washed from around the trees, we often +see the upper portion of the root covered with a thick bark and +fulfilling every office of a true stem. + +=67. Minute structure of the root.=—(_a_) Mount in water and place +under the microscope a portion of the root of an oat or radish +seedling containing a number of hairs. In studying the thin, +transparent roots of very young seedlings a section will not be +necessary. Observe whether the hairs originate from the epidermis or +from the interior. Are they true roots, or mere outgrowths from the +cells of the epidermis? Do they consist of a single cell or a number +of cells each? Notice what very thin cell walls the hairs have; is +there any advantage in this? The interior, transparent portion of +the hair contains the sap, and the protoplasm forms a thin lining on +the inner surface of the wall; why not the sap next the wall and the +protoplasm in the interior? (58, 60.) + +[Illustration: FIG. 79.—Longitudinal section through the tip of +a young root, somewhat diagrammatic: _h_, _h_, root hairs; _ep_, +epidermis; _a_, cortex; _b_, central cylinder; _e_, sheath of the +cylinder (endodermis); _g_, growing point; _c_, root cap; _d_, dead +and dying cells loosened from the extremity of the cap.] + +(_b_) Next examine a portion of the body of the root and try to +make out the parts as shown in Fig. 79, and compare them with your +observations in 64. The light line running through the middle is +the _central cylinder_, up which the water passes, as was shown by +the colored liquid in 64. Outside this is a darker portion (_a_, +Fig. 79), corresponding to the cortex (_rr_, Fig. 77). Besides other +uses, the cortex serves to prevent the loss of water as it passes up +to the stem, and also, in fleshy roots like the carrot and turnip, +for the storage of nourishment. Its innermost row of cells is +thickened into the sheath, or _endodermis_ (_e_), which serves as an +additional protection to the conducting tissues. The extreme outer +layer, from the cells of which the root hairs are developed, is, as +already stated, the epidermis, and in the older and more exposed +parts of perennial roots is displaced by the bark, which becomes +indistinguishable from that of the stem. (66.) + +(_c_) Look at the tip of the root for a loose structure (_c_) fitting +over it like a thimble. This is the rootcap. Do you see any loose +cells that seem to have broken away from it? These are old cells that +have been pushed to the front by the formation of new growth back of +them, and, being of no further use, are rubbed off by friction as the +root bores its way through the soil. Draw a longitudinal section of +the root as it appears under the microscope, labeling all the parts. +If they cannot be made out distinctly in the specimen examined, use +sections of young corn or bean roots, which are larger and show the +parts more distinctly. + +[Illustration: FIG. 80.—Cross section of a young root, magnified: +_h_, hairs; _a_, cortex; _b_, central cylinder; _e_, sheath or +endodermis; _ep_, epidermis; _sp_, cut ends of the ducts.] + +(_d_) Place under the microscope a thin cross section through the +hairy portion of a primary root of a bean or pea seedling, and try +to make out the parts noted above and shown in cross section in +Fig. 80. Make a sketch of what you see, labeling all the parts you +can recognize. Show in your drawing the differences in the size +and shape of the cells composing the different tissues. Notice in +the central cylinder (Fig. 80) several groups of what look in the +section like little round pits, or holes, _sp_. These are the cut +ends of large-sized tubes or _ducts_ that convey the water absorbed +by the roots to the stem. Each set of these tubes, together with a +number of smaller ones belonging to the same group, constitutes a +_fibrovascular bundle_—a very important element in the structure of +all roots and stems, as these bundles make up the conducting system +of the plant body. + + + IV. THE WORK OF ROOTS + + MATERIAL.—Germinating seedlings of radish, bean, corn, etc.; + a potted plant of calla, fuchsia, tropæolum, touch-me-not + (_Impatiens_), or corn; a plant that has been growing for some time + in a porous earthen jar. + + APPLIANCES.—Glass tumblers; coloring fluid; wax; some coarse + netting; dark wrapping paper, or a long cardboard box; a sheet of + oiled paper; some half-inch glass tubing; a few inches of rubber + tubing; an ounce of mercury; some blue litmus paper; a flower pot + full of earth; a few handfuls of sand, clay, and vegetable mold; a + pair of scales; a half dozen straight lamp chimneys, or long-necked + bottles from which the bottoms have been removed as directed in + Exp. 53. + + EXPERIMENT 43. USE OF THE EPIDERMIS.—Cut away the lower end + of a taproot; seal the cut surface with wax so as to make it + perfectly water-tight, and insert it in red ink for at least half + the remaining length, taking care that there is no break in the + epidermis. Cut an inch or two from the tip of the lower piece, or + if material is abundant, from another root of the same kind, and + without sealing the cut surface, insert it in red ink, beside the + other. At the end of three or four hours, examine longitudinal + sections of both pieces. Has the liquid been absorbed equally by + both? If not, in which has it been absorbed the more freely? What + conclusion would you draw from this, as to the passage of liquids + through the epidermis? + + From this experiment we see that the epidermis, besides protecting + the more delicate parts within from mechanical injury by hard + substances contained in the soil, serves by its comparative + imperviousness to prevent evaporation, or the escape of the sap by + osmosis as it flows from the root hairs up to the stem and leaves. + + EXPERIMENT 44. TO SHOW THAT ROOTS ABSORB MOISTURE.—Fill two pots + with damp earth, put a healthy plant in one, and set them side by + side in the shade. After a few days examine by digging into the + soil with a fork and see in which pot it is drier. Where has the + moisture gone? How did it get out? + + EXPERIMENT 45. TO SHOW THAT ROOTS SHUN THE LIGHT.—Cover the top + of a glass of water with thin netting, and lay on it sprouting + mustard or other convenient seed. Allow the roots to pass through + the netting into the water, noting the position of root and stem. + Envelop the sides of the glass in heavy wrapping paper, admitting + a little ray of light through a slit in one side, and after a few + days again observe the relative position of the two organs. How is + each affected by the light? + + EXPERIMENT 46. TO FIND OUT WHETHER ROOTS NEED AIR.—Remove a plant + from a porous earthenware pot in which it has been growing for some + time; the roots will be found spread out in contact with the walls + of the pot instead of embedded in the soil at the center. Why is + this? + + EXPERIMENT 47. TO SHOW THAT ROOTS SEEK WATER.—Stretch some coarse + netting covered with moist batting over the top of an empty + tumbler. Lay on it some seedlings, as in Exp. 45, allowing the + roots to pass through the meshes of the netting. Keep the batting + moist, but take care not to let any of the water run into the + vessel. Observe the position of the roots at intervals, for twelve + to twenty-four hours, then fill the glass with water to within + 10 millimeters (a half inch, nearly) or less of the netting, let + the batting dry, and after eight or ten hours again observe the + position of the roots. What would you infer from this experiment as + to the affinity of roots for water? + + EXPERIMENT 48. WHAT BECOMES OF THE WATER ABSORBED BY ROOTS.—Cover + a calla lily, young cornstalk, sunflower, tropæolum, or other + succulent herb with a cap of oiled paper to prevent evaporation + from the leaves, set the pot containing it in a pan of tepid water, + and keep the temperature unchanged. After a few hours look for + water drops on the leaves. Where did this water come from? How did + it get up into the leaves? + + EXPERIMENT 49. TO SHOW THE FORCE OF ROOT PRESSURE.—Cut off the stem + of the plant 6 or 8 centimeters (3 or 4 inches) from the base. Slip + over the part remaining in the soil a bit of rubber tubing of about + the same diameter as the stem, and tie tightly just below the cut. + Pour in a little water to keep the stem moist, and slip in above, + a short piece of tightly fitting glass tubing. Watch the tube for + several days and note the rise of water in it. The same phenomenon + may be observed in the “bleeding” of rapidly growing, absorbent + young shoots, such as grape, sunflower, gourd, tobacco, etc., if + cut off near the ground in spring when the earth is warm and moist. + By means of an arrangement like that shown in Fig. 81, the force + of the pressure exerted can be measured by the displacement of the + mercury. This flow cannot be due to the giving off of moisture + by the leaves, since they have been removed. Their action, when + present, by causing a deficiency of moisture in certain places may + influence the direction and rapidity of the current, but does not + furnish the motive power, which evidently comes, in part at least, + from the roots, and is the expression of their absorbent activity. + +[Illustration: FIG. 81.—Arrangement for estimating the force of root +pressure: _s_, stub of the cut stem; _g_, glass tubing joined by +means of the rubber tubing, _t_, to the stem; _m_, mercury forced up +the glass tube by water, _w_, pumped from the soil by the roots.] + + EXPERIMENT 50. TO SHOW THAT ROOTS CAUSE THE OCCURRENCE OF + ACIDS.—Lay a piece of blue litmus paper on a board or on a piece + of glass slightly tilted at one end to secure drainage. Cover the + surface with an inch of moist sand and plant in it a number of + healthy seedlings. Acids have the property of changing blue litmus + to red; hence, if you find any red stains on the paper where the + roots have penetrated, what are you to conclude? + + Carbon dioxide has a slight acid reaction and is caused to form in + varying quantities by all roots. Probably other substances, and + these not a few, are actually excreted. + + EXPERIMENT 51. CAN THE ABSORBENT POWER OF ROOTS BE INTERFERED + WITH?—Place the roots of a number of seedlings with well-developed + hairs in a weak solution of saltpeter—10 grams (about ⅓ of an + ounce) to a pint of water, and others in a stronger solution—say 30 + grams, or 1 ounce, to a pint. Try the same experiment with weak and + strong solutions of any conveniently obtainable liquid fertilizer. + After 45 minutes or an hour examine the roots under a lens and note + the change that has taken place. What has gone out of them? What + caused the loss of the contained sap? + + EXPERIMENT 52. TO TEST THE WEIGHT OF SOILS.—Thoroughly dry and + powder a pint each of sand and clay, measure accurately, and + balance against each other in a pair of scales. Which weighs more, + bulk for bulk, a “light” soil, or a “heavy” one? (77.) + + EXPERIMENT 53. TO TEST THE CAPACITY OF SOILS FOR ABSORBING AND + RETAINING MOISTURE.—Arrange, as shown in Fig. 82, a number of + long-necked bottles from which the bottom has been removed. This + can be done by making a small indentation with a file at the point + desired and leading the break round the circumference with the end + of a glowing wire or a red-hot poker. The crack will follow the + heated object with sufficient regularity to answer the purpose. + Tie a piece of thin cloth over the mouth of each bottle and invert + with the necks extending an inch or two into empty tumblers placed + beneath. Fill all to the same height with soils of different + kinds—sand, clay, gravel, loam, vegetable mold, etc.—and pour over + each the same quantity of water from above. Watch the rate at which + the liquid filters through into the tumblers. Which loses its + moisture soonest? Which retains it longest? + +[Illustration: FIG. 82.—Apparatus for testing the capacity of soils +to take in and retain moisture.] + + Next leave the soils in the bottles dry, fill the tumblers up to + the necks of the bottles, and watch the rate at which the water + rises in the different ones. The power of soils to absorb moisture + is called _capillarity_. Which of your samples shows the highest + capillarity? Which the lowest? Do you observe any relation between + the capillarity of a soil and its power of retention? + +=68. Roots as holdfasts.=—One use of ordinary roots is to serve as +props and stays for anchoring plants to the soil. Tall herbs and +shrubs, and vegetation generally that is exposed to much stress of +weather, are apt to have large, strong roots. Even plants of the same +species will develop systems of very different strength according as +they grow in sheltered or exposed places. + +[Illustration: FIG. 83.—Dandelion: _a_, common form, grown in plains +region at low altitude; _b_, alpine form.] + +=69. Root pull.=—Roots are not mere passive holdfasts, but exert +an active downward pull upon the stem. Notice the rooting end of a +strawberry or raspberry shoot and observe how the stem appears to +be drawn into the ground at the rooting point. In the leaf rosettes +of herbs growing flat on the ground or in the crevices of walls and +pavements, the strong depression observable at the center is due to +root pull. (Fig. 84.) + +[Illustration: FIG. 84.—Raspberry stolon showing root pull.] + +=70. Storage of food.=—Another office of roots is to store up food +for the use of the plant. This is done chiefly in the tissues of +fleshy roots and tubers, and gives to them their great economic +value. Next to grains and cereals, roots probably furnish a larger +portion of food to the human race than any other crop. In addition to +this they are also the source of valuable drugs, condiments, and dyes. + +=71. Absorption and conveyance of sap.=—But the most important +function of roots is that of absorption. By their action the soil +water and the minerals contained in it are drawn up into the plant +body and made available for conversion by the leaves into organic +foods, as will be explained in another chapter. From the nature +of their function, most roots have naturally a strong affinity +for water, and its presence or absence has a marked influence on +their direction of growth, being often sufficient to overcome that +of geotropism (Exp. 47). There are many trees and shrubs, notably +willow, sweet bay, red birch, and the like, that grow best on the +banks of streams and ponds, where their roots can have direct access +to water. Excess of moisture, however, is injurious to most land +plants by preventing the roots from getting sufficient air for +respiration. + +=72. The conditions of absorption.=—The sap in the root cells is +normally denser than the water in the soil, so there is a continuous +flow from the latter to the former. But if, for any reason, the +density of the liquids should be reversed, the flow would set in the +opposite direction, and if continued long enough, the strength of the +plant would be literally “sapped” by the exhaustion of its tissues, +so that it would die. What is this process of cell exhaustion called? + +=73. The use of acid secretions to the root.=—It was shown in Exp. +50 that carbon dioxide and probably other substances occur in the +immediate vicinity of roots. Carbon dioxide is an active agent in +dissolving the various mineral matters contained in the soil, and as +these last can be absorbed only in a liquid or a gaseous state (63), +the advantage to the root as an absorbent organ, of being able to +secrete such active solvents, is obvious. + +[Illustration: FIG. 85.—A natural root etching, found on a piece of +slate.] + +=74. Relation of roots to the soil.=—In order to perform their work +of absorption, roots must have access to a suitable soil. To produce +the best results a soil must contain (1) all the essential mineral +constituents (62); (2) moisture for dissolving these materials; and +(3) air enough to supply the oxygen which is necessary to the life +processes of all green plants. + +=75. Composition of soils.=—Sand, clay, and humus, or vegetable +mold, with the various substances dissolved in them, constitute the +basis of cultivated soils. A mixture of sand, clay, and humus is +called loam. When the proportion of humus is very large and well +decomposed, the mixture is called _muck_. Pure sand contains but +little nourishing matter and is too porous to retain water well. Pure +clay is too compact to be easily permeable to either air or water. +Most soils are composed of a mixture of the two with vegetable mold +in varying proportions, giving a sandy loam, or a clay loam, as the +case may be. + +=76. Tillage.=—The advantages of tillage are: (_a_) that by breaking +up the hard lumps it renders the soil more permeable to air and water +and more easily penetrable by the roots in their search for food; +(_b_) the covering of loose, friable earth left by the plow and the +harrow acts as a mulch, and by shading the soil below, prevents +too rapid a loss of water by evaporation. Where the essential food +ingredients are present, good tillage counts for more in making a +crop than the original quality of the soil. + +=77. Light and heavy soils.=—These terms are used by farmers not +in relation to the weight of soils, but in reference to the ease +or difficulty with which they are worked. Light soils contain a +preponderance of sand; heavy ones, of clay. + + + Practical Questions + + 1. Will plants grow better in an earthen pot or a wooden box than + in a vessel of glass or metal? Why? (Exp. 46.) + + 2. Which absorb more from the soil, plants with light roots and + abundant foliage, or those with heavy roots and scant foliage? + (Suggestion: roots absorb from the soil; leaves, mainly from the + air.) + + 3. Why are willows so generally selected for planting along the + borders of streams in order to protect the banks from washing? (71.) + + 4. Why are the conducting tissues of roots at the center instead of + near the surface as in stems? (67, _b_.) + + 5. Why does corn never grow well in swampy ground? (74; Exp. 46.) + + 6. Why are fleshy roots so much larger in cultivated plants than in + wild ones of the same species? (74, 76.) + + 7. When the use of a particular kind of fertilizer causes the + leaves of the plants to which it has been applied to turn brown, so + that the farmer says they have been “burned” by it, to what cause + is the trouble due? (59, 72.) + + 8. Why do farmers speak of turnips and other root crops as “heavy + feeders”? (70, 71.) + + 9. Which is more exhausting to the soil, a crop of beets, or one of + oats? Onions, or green peas? (See 2, suggestion.) + + 10. Why will inserting the end of a wilted twig in warm water + sometimes cause it to revive? (Exps. 48, 49.) + + + V. DIFFERENT FORMS OF ROOTS + + MATERIAL.—Examples of taproots: bean, pea, cotton, maple seedlings, + or any kind of very young woody root. Fibrous: any kind of grass + or grain. Fleshy: parsnip, turnip, carrot, dahlia, sweet potato. + Water: duckweed, pondweed, or a cutting of wandering Jew grown + in water. Parasitic: mistletoe, dodder, beech drops. Aërial and + adventitious: the aërial roots of old scuppernong vines, climbing + roots of ivy and trumpet vine, prop roots from the lower nodes of + cornstalks and sugar cane. + +=78. Basis of distinction.=—Roots vary in form and external structure +according to their origin, function, and surroundings. In reference +to the first, they are classed as primary or secondary; in regard to +the second, as dry or fleshy; while as to surroundings, they may be +adapted to either the soil, water, air, or the parasitic habit. Soil +roots are the normal form. According to their mode of growth they are +either fibrous or axial. + +[Illustration: PLATE 3.—Aërial roots of a Mexican “strangling” fig, +enveloping the trunk of a palm (_From_ “Rep’t. Mo. Bot. Garden”).] + +=79. Taproots.=—These are the common form of the axial type. Compare +the root of any young hardwood cion a year or two old with one +of a mature stalk of corn or other grain, and with the roots of +seedlings of the same species. Notice the difference in their mode +of growth. In the first kind a single stout prolongation called a +taproot proceeds from the lower end of the hypocotyl and continues +the axis of growth straight downward, unless turned aside by some +external influence. A taproot may be either simple, as in the turnip, +radish, and dandelion, or branched, as in most shrubs and trees. In +the latter case the main axis is called the primary root, and the +branches are secondary ones. + +[Illustration: FIG. 86.—Branched taproot of maple.] + +=80. Fibrous and fascicled roots.=—Where the main axis fails +to develop, as in the corn and grasses generally, a number of +independent branches take its place, forming what are known as +fibrous roots. Both fibrous and taproots may be either hard or +fleshy. The turnip and carrot are examples of fleshy taproots, the +dahlia and rhubarb of fascicled roots. The function of both is the +storage of nourishment. The sweet potato is an example of a tuberous +root. + +=81. Practical importance of this distinction.=—The difference +between axial and fibrous roots has important bearings in +agriculture. The first kind, which are characteristic of most +dicotyls, strike deep and draw their nourishment from the lower +strata of the soil, while the fibrous and fascicled, or radial kinds, +as we may call them for want of a better name, spread out near the +surface and are more dependent on external conditions. + +[Illustration: FIG. 87.—Fibrous root.] + +=82. Roots that grow above ground.=—The kinds of roots that have +just been considered are all subterranean, and bring the plant +into relation with the earth, whether for the purpose of absorbing +nourishment, or of mechanical support, or, as in the majority of +cases, for both. Many plants, however, do not get their mineral +nutrients directly from the soil, and these give rise to various +forms suited to other conditions of alimentation. + +=83. Adventitious roots.=—This name applies to any kinds of roots +that occur on stems, or in other unusual positions. They may be +considered as intermediate between the two classes named in 81; for +while their starting point is above ground, they generally end by +fixing themselves in the soil, where they often function as normal +roots. Familiar examples are the roots that put out from the lower +nodes of corn and sugar cane stalks, and serve both to supply +additional moisture and to anchor the plant more firmly to the soil. +Most plants will develop adventitious roots if covered with earth, or +even if merely kept in contact with the ground. The gardener takes +advantage of this capacity when he propagates by cuttings and layers. + +=84. Water roots.=—These are generally white and threadlike and more +tender and succulent than ordinary soil roots, because they have less +work to do. Floating and immersed plants, such as bladderwort and +hornwort (_Ceratophyllum_) have no need of absorbent roots, since the +greater part of their surface is in contact with water and can absorb +directly what is needed. + +Land plants will often develop water roots and thrive for a time if +the liquid holds in solution a sufficient quantity of air and mineral +nutrients. Place a cutting of wandering Jew in a glass of clear +water, and in from four to six days it will develop beautiful water +roots in which both hairs and cap are clearly visible to the naked +eye. + +=85. Haustoria=, from a Latin word meaning to drain, or exhaust, +is a name given to the roots of parasitic plants, or such as live +by attaching themselves to some other living organism, from which +they draw their nourishment ready made. Their roots are adapted +to penetrating the substance of the _host_, as their victim is +called, and absorbing the sap from it. Dodder and mistletoe are the +best-known examples of plant parasites, though the latter is only +partially parasitic, as it merely takes up the sap from the host and +manufactures its own food by means of its green leaves. + +[Illustration: FIG. 88.—Beech root: _A_, grown in unsterilized wood +humus: _p_, strands of fungal hyphæ, associated at _a_, with humus; +_B_, grown in wood humus freed from fungus by sterilization—it is not +provided with fungal hyphæ, and has root hairs, _h_. (_A_ and _B_ +both several times magnified.)] + +=86. Saprophytes.=—Akin to parasites are saprophytes, which live +on dead and decaying vegetable matter. They are only partially +parasitic and do not bear the haustoria of true parasites. Many of +them, of which the Indian pipe (_Monotropa_) and coral root are +familiar examples, obtain their nourishment in part, at least, by +association with certain saprophytic fungi, which enmesh their roots +in a growth of threadlike fibers that take the place of root hairs +and absorb organic food from the rich humus in which these plants +grow. Such growths are called _mycorrhiza_, meaning “fungal roots.” +Similar associations are formed by some of the higher plants also. +The rootlets of the common beech and of certain of the pine family, +for instance, are often enveloped in a network of fungus fibers, +and in this case root hairs are developed very poorly, or not at +all. Besides greatly increasing the absorbent surface by their +ramification through the soil, the mycorrhizal threads may possibly +benefit the plant in other ways also, as, for instance, by bringing +about chemical changes that might aid in the work of nutrition. + +[Illustration: FIG. 89.—An air plant (_Tillandsia_), growing on the +underside of a bough.] + +[Illustration: FIG. 90.—A single strand of _Tillandsia usneoides_, a +rootless epiphyte belonging to the pineapple family; better known as +the “Spanish moss” that drapes the boughs of trees so conspicuously +in the warm parts of America. Two-thirds natural size. (Photographed +by C. F. O’Keefe.)] + +=87. Epiphytes, or air plants.=—In the proper meaning of the word +these are not parasitic, but use their host merely as a mechanical +support to bring them into better light relations. The name, however, +is loosely applied to all plants that find a lodgment on the trunks +and branches of trees, whether parasites or true epiphytes that draw +no nourishment from the host. Not infrequently the latter is killed +by them through suffocation, overweighting, or the constriction of +the stems by close clinging twiners. + +=88. Aërial roots= are such as have no connection at all with the +soil or with any host plant, except as they may lodge upon the trunks +and branches of trees for a support. In other than purely epiphytic +plants, which get all their nourishment from the air, they are +generally subsidiary to soil roots, like the long dangling cords that +hang from some species of old grapevines; or they subserve other +purposes altogether than absorbing nourishment, as the climbing roots +of the trumpet vine and poison ivy. A very remarkable development +of aërial roots takes place in the “strangling fig” of Mexico and +Florida, which begins life as a small epiphyte, from seeds dropped by +birds on the boughs or trunks of trees. When it gets well started, +the young plant sends down enormous aërial roots, which find their +way to the ground, and in time so completely envelop the host that it +is literally strangled to death (Plate 3, p. 73). When this support +is removed, the sheathing roots take its place and become to all +intents and purposes the stem of the fig tree, which now leads an +independent life. + +[Illustration: FIG. 91.—Root system of a tobacco plant.] + +=89. The root system.=—The entire mass of roots belonging to a +plant, with all its ramifications and subdivisions, composes a root +system. The extent of root expansion is in general about equal to +that of the crown, thus bringing the new and active parts under the +drip of the boughs where the moisture is most abundant. Some plants +have root systems out of all seeming proportion to their size. A +catalpa seedling six months old showed, by actual measurement, +250 feet of root growth, and it is estimated that the roots of a +thrifty cornstalk, if laid end to end, would extend a mile. In the +development of the root system, a great deal depends upon external +conditions. In a poor, dry soil, the roots have to travel farther in +search of a livelihood, and so a larger system has to be developed +than in a more favorable location. + + + Practical Questions + + 1. Which is better to succeed a crop of turnips on the same land, + hay or carrots? (81.) + + 2. Write out what you think would be a good rotation for four or + five successive crops based on the forms of the roots. + + 3. Study the following rotations and give your opinion about them, + on the same principle. Suggest any improvements that may occur + to you, and give a reason for the change. Beets, barley, clover, + wheat; cotton, oats, peas, corn; oats, melons, turnips; cotton, + oats, corn and peas mixed, melons; cotton, hay, corn, peas. + + 4. Give three good reasons in favor of a rotation over a + single-crop system. (24, 60, 62, 81.) + + 5. Which will require deeper tillage, a bed of carrots or one of + strawberries? (81.) + + 6. Explain why some plants keep green and fresh when the surface of + the soil is dry, while others wilt or die. (81, 89.) + + 7. Which will better withstand drought, a crop of alfalfa or one of + Indian corn? Why? (81.) + + 8. Which will interfere less with the trees if planted in an + orchard, beets or onions? (81.) + + 9. Ought a crop of hemp and tobacco to succeed each other on the + same land? (81, 89.) + + 10. Why does a gardener manure a grass plot by scattering the + fertilizer on the surface, while he digs around the roses and + lilacs and deposits it under ground? (81.) + + 11. Do the adventitious roots of such climbers as ivy and trumpet + vine draw any nourishment from the objects to which they cling? + (83-88.) + + 12. How can you tell? + + 13. Do partial dependents of this kind injure trees by climbing + upon them; and if so, how? (87, 88.) + + 14. What is the use of the aërial roots of the scuppernong grape? + (88.) + + 15. Is the resurrection fern (_Polypodium incanum_), that grows on + tree trunks in our Southern States, a parasite or an air plant? + (87.) + + 16. On what plants in your neighborhood does mistletoe grow most + abundantly? Dodder? + + 17. Is mistletoe injurious to the host? (85.) + + 18. Name some plants that are propagated mainly, or solely, by + roots and cuttings. + + 19. Where do aërial roots get their nourishment? (88.) + + 20. Would they be of any use to a plant in a very cold or dry + climate? + + 21. Where should manure be placed to benefit a tree or shrub with + wide-spreading roots? (66, 89.) + + 22. Is it a wise practice to mulch a tree by raking up dead leaves + and piling them around the base of the trunk, as is often done? + Why, or why not? (66, 89.) + + + Field Work + + (1) Examine the underground parts of hardy winter herbs in your + neighborhood, also of any weeds or grasses that are particularly + troublesome, and see if there is anything about the structure of + these parts to account for their persistence. Note the difference + between roots of the same species in low, moist places and in + dry ones; between those of the same kind of plants in different + soils; in sheltered and in exposed situations. Study the direction + and position of the roots of trees and shrubs with reference to + any stream or body of water in the neighborhood. (The elm, fig, + mulberry, and willow are good subjects for such observations.) + Notice also whether there is any relation between the underground + parts and the leaf systems of plants in reference to drainage and + transpiration. + + (2) Observe the effect of root pull upon low herbs. Look along + washes and gullies for roots doing the office of stems, and note + any changes of structure consequent thereon. Study the relative + length and strength of the root systems of different plants, with + reference to their value as soil binders, or their hurtfulness in + damaging the walls of cellars, wells, sewers, etc. Dig your trowel + a few inches into the soil of any grove or copse you happen to + visit, note the inextricable tangle of roots, and consider the + fierce competition for living room in the vegetable world that it + implies. + + (3) Tests might be made of the different soils in the neighborhood + of the schoolhouse by planting seeds of various kinds and noting + the rate of germination; first, without fertilizers, then by adding + the different elements in succession to see what is lacking. The + field for study suggested by this subject is almost inexhaustible. + + + + +CHAPTER IV. THE STEM + + + I. FORMS AND GROWTH OF STEMS + + MATERIAL.—Vigorous young hop or beau seedlings grown in pots; a + fresh dandelion stalk; a stem of pea, squash, cucumber, grape, or + passion flower vine, with tendrils. + + APPLIANCES.—A bowl of fresh water; rods of different sizes and + smoothness for testing the hold of climbers. + + EXPERIMENT 54. TO SHOW THE MOVEMENTS OF TWINING STEMS.—Raise a + young hop or bean seedling in the schoolroom and allow it to grow + about two decimeters—8 to 10 inches—in length before providing + it with a support. Does the stem form any coils? Bring it in + contact with a suitable upright support and watch for a day or + two. What happens? Notice whether it starts to coil from right to + left or from left to right and see if you can coax it to turn in + the opposite direction. When it has reached the end of its stake, + allow it to grow about five centimeters (two inches, approximately) + beyond, and watch the revolution of the tip. Cut a hole through the + center of a piece of cardboard about 14 centimeters (five to six + inches) in diameter, slip it over the loose end of the stem, and + fasten it to the stake in a horizontal position, with a pin. Note + the position of the stem tip at regular intervals and mark on the + cardboard; how long does it take to complete a revolution? Does it + continue to coil, or to coil as readily, after leaving its stake as + before? What would you infer from this as to the effect of contact + in stimulating it to coil? + + Find out by experiment if it can climb well by means of a glass or + other smooth rod; by a fine wire; a broomstick; a large, smooth + post. See whether it does better on a horizontal or an upright + support. + + EXPERIMENT 55. TO ILLUSTRATE THE COILING OF STEMS.—Run a gathering + thread in one side of a narrow strip of muslin and notice how the + ruffle thus drawn will curl into a spiral when allowed to dangle + from the needle. Can you think of any cause that might act on a + stem in the same way? Suppose, for instance, that one side should + grow faster than the other; what would be the effect? (54.) + + Split the stem of a fresh dandelion, or other herbaceous scape, + longitudinally, and immerse it in a pan of fresh water for a few + minutes. Notice how the two halves curve outward, or even coil up + like the strip of muslin. This is due to the tension caused by the + more rapid absorption of the thinner walled cells of the internal + tissues. These, when relieved of the resistance of the thicker + walled outer tissues, swell on their free side, but are held back + on the other by the non-absorbent outer parts, as one side of the + muslin ruffle was held by the gathering thread. + + EXPERIMENT 56. TO FIND OUT WHETHER THE DIRECTION OF STEM GROWTH IS + INFLUENCED BY LIGHT.—Place two rapidly growing young pea, bean, + sunflower, or squash plants, each with several well-developed + leaves, in a room or box with a light exposure on one side only. + After two or three days, notice the position of the stems in regard + to the light. Does either one show a more decided inclination + toward it than the other? + + EXPERIMENT 57. IS THE LIGHT RELATION OF THE STEM INFLUENCED BY THE + LEAVES?—Cut the leaves from one of the plants used in Exp. 56, + covering the cut surfaces with vaseline to prevent “bleeding”; + reverse the positions of both with regard to the light, and watch + for two or three days. In which is the response to light the more + rapid? What does this indicate as one object of the stem in seeking + light? What is the best position of a stem, ordinarily, for getting + its leaves into the light? + +[Illustration: FIG. 92.—Stems of red oak and hickory that have +grafted themselves.] + +=90. Classification.=—Stems are classed according to (1) duration, as +annuals, biennials, and perennials; (2) with reference to hardness +or softness of structure, as herbaceous and woody; (3) in regard to +position and direction of growth, as erect, prostrate, climbing, +inclined, declined, underground, etc. + +=91. Annuals= complete their life cycle in a single season and then +die down as soon as they have perfected their seed. Many of our most +troublesome weeds belong to this class and might be exterminated +by the simple expedient of mowing them down before their time of +flowering. + +=92. Biennials=, as the name implies, live for two years. Their +energy during the first season is spent chiefly in laying by a store +of nourishment, usually in the tissues of fleshy roots (70). By this +means they get a good start in the second season and mature their +seeds early. Many of our common garden vegetables, such as turnips, +carrots, parsnips, and cabbage, belong to this class. Where is the +nourishment stored in the cabbage? + +[Illustration: FIG. 93.—A biennial plant, mullein, in winter +condition with stem reduced to little more than a disk supporting +a rosette of leaves. Notice how close they cling to the earth, and +compare them with their fruiting condition a few months later as +shown in Fig. 237.] + +=93. Perennials= are plants that live on indefinitely, like most of +our forest trees and woody-stemmed shrubs. Woody stems are usually +perennial and may live for hundreds and even thousands of years, as +those of the giant sequoias of California, and the famous chestnut of +Mt. Etna. + +=94. Herbaceous stems= are more or less succulent and die down after +fruiting. They are usually annuals, though some kinds, like the +garden geraniums and the common St.-John’s-wort, show a tendency +to become woody, especially at the base, and live on from year to +year. Others, such as the hawkweed and dahlia, die down above ground +in winter, but are enabled to keep their underground parts alive +indefinitely, through the nourishment stored in them, and are thus +perennial below ground and annual above. Woody-stemmed annuals, such +as the cotton and castor oil plant, are not, properly speaking, +herbs. In the tropical countries to which they belong they are +perennial shrubs, or even small trees, but on being transplanted to +colder regions have been compelled to take on the annual habit as an +adaptation to climate. + +[Illustration: FIG. 94.—Orange hawkweed with runners.] + +[Illustration: FIG. 95.—Prostrate stem of Lycopodium with assurgent +branches.] + +[Illustration: FIG. 96.—Diagram of stem growth: _ps_, surface of the +ground; _e_, erect position; _d_, declined; _a_, assurgent; _p_, +prostrate; _u_, vertical direction underground.] + +=95. Direction and habit of growth.=—As to manner of growth, there +are many forms, from the upright boles of the beech and pine to the +trailing, prostrate, and creeping stems of which we have examples +in the running periwinkle, the prostrate spurge and the creeping +partridge berry (_Mitchella repens_), respectively. Trailing and +prostrate stems are very apt to become creepers by the development of +adventitious roots at their nodes wherever they come in contact with +the soil. The rooting stems of dewberries, the runners and stolons of +strawberries and currants, are familiar examples. + +Between the extremes of prostrate and upright, stems may be inclined +or bent in various degrees. As shown in Fig. 96, there are two modes +of inclination: _assurgent_, _a_, from the prostrate, _p_, toward +the upright, _e_; and _declined_, _d_, from the upright toward the +prostrate. Below the surface, _ps_, occur only underground stems. Is +the prostrate habit an advantageous one for light exposure? Can you +think of any compensating advantages a plant might derive from it; +for example, in regard to warmth and moisture? + +[Illustration: FIG. 97.—Twining stems: _A_, hop twining with the sun; +_B_, convolvulus twining against the sun.] + +=96. Climbing stems.=—These are such as lift themselves from the +ground and attain the advantages of the upright position by clinging +to supports of various kinds—usually, in a state of nature, the +stems and boughs of other plants. The means of climbing may be: +(1) by merely leaning upon or propping themselves up by the aid of +the supporting object—examples, the rose, wistaria, star jessamine +(_Jasminum officinalis_); (2) by coiling their main axes spirally +around the support—hop, bean, morning-glory; (3) by means of +adventitious roots—poison ivy, common English ivy, trumpet vine +(_Tecoma radicans_); (4) by organs specially developed for the +purpose, called tendrils—gourd, cucumber, grape, passion flower. + +[Illustration: FIG. 98.—Leaf of common pea, showing upper leaflets +reduced to tendrils.] + +=97. Tendrils.=—The part assigned to do the work of climbing may be +a secondary branch, a flower stem, a leafstalk, a leaf, a leaflet, +or a group of leaflets (Fig. 98). Tendrils behave in general very +much like twining stems, except that they are more sensitive and +respond more quickly to any cause that may influence their movement. +While young, their tips revolve just as do the tips of twining stems, +until they meet with an object round which they can coil. When this +happens, not only the part in contact with the object coils, but +the free part between it and the main axis will usually respond by +twisting itself into a helix (Fig. 99). As the distance between the +base and tip of the tendril is shortened by coiling, the body of +the plant is drawn upward proportionally. It will be observed that +the helix is interrupted at one or more points, above and below +which the coils turn in opposite directions. This is because the +tendril is attached at both ends and cannot adjust itself to the +opposite strains of torsion. Twist with your fingers a piece of tape +so attached, and you will see that on one side of your hand it turns +from right to left and on the other from left to right. + +=98. The cause of twining.=—Botanists are not fully agreed on this +point. The explanation most generally accepted at present is that +the twining of stems is due to the combined action of lateral and +negative geotropism (51). The first causes one side to grow more +rapidly than the other, thus forming a succession of coils, while +the second, by stimulating the upward growth of the axis, stretches +it into a spiral, and in this way draws it more tightly round the +support. For this reason twining stems do best on an upright support. + +[Illustration: FIG. 99.—Stems of a passion flower transformed into +tendrils. (_After_ GRAY.)] + +In tendrils, the twining is thought to be due not to gravity, but to +contact with a solid body, which, by inducing unequal development +on opposite sides of the tendril, causes it to turn about an +available object. The coiling of the free part of the twining +organ is in response to the stimulus transmitted from the part in +contact—_stimulus_, in this sense, denoting the influence of any +external agent that calls forth a responsive adjustment on the part +of the plant. + +[Illustration: FIG. 100.—Showing the economy of labor and building +material effected by the climbing habit. Notice how the grapevine +coils like an anaconda around the tree boles, and overtops their +tallest branches. Compare the diameter of the vine with that of the +trees.] + +=99. The object of the various habits of stem growth.=—To bring +the growing parts of the plant into the best possible relations +with light and air is one of the special functions of the stem, and +the various habits of growth described in this section have been +developed with reference to this function. In the case of prostrate +and underground stems other factors may intervene; can you name some +of the causes that might influence the position of the stem in such +cases? + + + Practical Questions + + 1. Why is the normal direction of most stems upright? (Exp. 56.) + + 2. Name a dozen woody-stemmed plants; a dozen with herbaceous stems. + + 3. Name all the plants you can think of that have prostrate stems, + or leaf rosettes that hug the earth, like mullein and dandelion. + Which of these are wintergreen plants? Which are hot-weather + growers? + + 4. Can you explain in what ways both hot-weather and cold-weather + plants may be advantaged by the habit of clinging close to the + earth? (94, 95.) + + 5. Is there any difference in the height of the stem of a dandelion + flower and a dandelion ball? + + 6. Of what advantage is this to the plant? (Exp. 17.) + + 7. Name all the means you can think of by which a stem may climb, + and give an example of each. + + 8. Why do we support peas with brush, and hops or beans with poles? + (98; Exp. 54.) + + 9. Are the vines of gourds, watermelons, squashes, and pumpkins + normally climbing or prostrate? How can you tell? (96, 97.) + + 10. Why does not the gardener provide them with poles or trellises + to climb on? + + 11. Do twining plants grow equally well on horizontal and upright + supports? (98; Exp. 54.) + + 12. If there is any difference, which do they seem to prefer? + + 13. Can you give any reasons for thinking that the climbing habit + might lead to parasitism? (83, 85, 87.) + + 14. What method of climbing would be most favorable to the + development of such a habit? (Suggestion: What mode of climbing + brings the stem into closest contact with its support?) + + 15. Name some plants the stems of which are used as food. + + 16. Name some from which gums and medicines are obtained. + + 17. Explain how it can benefit a plant to have its leaves, or some + of them, modified into tendrils. (99.) + + 18. In what way is the loss of the normal function of the leaves so + modified, compensated for? (Exp. 57.) + + 19. Suppose the vine shown in Fig. 100 had to lift itself without + the aid of a support; could it reach the same height and carry the + same weight of foliage and flowers with the same expenditure of + labor and building material? + + + II. MODIFICATIONS OF THE STEM + + MATERIAL.—A shoot of asparagus; thorny branches of locust, plum, or + haw; a cactus plant; bulbs of lily and hyacinth or onion; tubers of + potato; rootstocks of iris, fern, or violet. If fresh specimens are + not accessible, dried rootstocks of the sweet flag and Florentine + iris may be obtained at the drug stores under the names of calamus + and “orris” root. + +=100. How to recognize modified parts.=—Stems, like roots, are often +modified to serve other than their normal purpose, and in adapting +themselves to these new functions they sometimes undergo such changes +of form and structure that it would be impossible to recognize their +true nature from appearances alone. The safest tests in such cases +are: (1) by a comparison of the parts of the modified structure with +those of known organs of the same kind; and (2) by observing its +position in reference to other parts. For instance, we know that +the stem is the part of the plant which normally bears leaves and +flowers, and if either of these, or if the small scales which often +take the place of leaves, are found growing on any plant structure, +we may usually take for granted that it is a stem. Then, again, as +will be shown in the next chapter, buds and branches naturally appear +only at the nodes, in or near the _axil_, or inner angle made by a +leaf with the stem. Hence, if you see any growth springing from such +a position, you may generally conclude it to be a stem. + +[Illustration: FIG. 101.—Stem-leaves (cladophylls) of a ruscus, +bearing flowers.] + +=101. Stems as foliage.=—The connection between stem and leaf is so +intimate that we need not be surprised to find a frequent interchange +of function between them, the leaf, or some part of it, doing the +work of the stem (Fig. 98), the stem more often taking upon itself +the office of the leaf. A common example is the garden asparagus. +Examine one of the young shoots sold in the market, and notice that +it bears a number of small scales in place of leaves. On an older +shoot that has gone to seed, the green, threadlike appendages, which +are usually taken for foliage, will be found to spring each from the +axil of one of these scales. What, therefore, are we to conclude that +it is? + +In the butcher’s-broom of Europe, the transformation has gone so far +that the branches of the stem have assumed the flattened appearance +of leaves (Fig. 101), but their real nature is evident both from +their position in the axils of leaf scales, and from the fact that +they bear flower clusters in the axil of a scale on their upper face. +Another example of this sort of modification is seen in the pretty +little _myrsiphyllum_ of the greenhouses (wrongly called smilax), +which is so much used for decoration. The delicate green blades are +merely altered stems, shortened and flattened to simulate leaves. + +[Illustration: FIG. 102.—Thorn branches of _Holocantha Emoryi_, a +plant growing in arid regions.] + +=102. Weapons of defense.=—Conspicuous examples of these are the +bristling thorns of the honey locust. Is their frequent branching +any indication of their real nature? Does it _prove_ anything, or +must you look for other evidence? What further indications might +you expect to find, if they are true branching stems? (100.) On old +haw, plum, crab, and pear trees, stems can be found in all stages +of transition, from stubby, ill-developed branches, to well-defined +thorns. + +[Illustration: FIG. 103.—Melon cactus, showing greatly condensed stem +for the storage and preservation of moisture.] + +=103. Storage of nourishment.=—This is one of the most frequent +causes of modification in both roots and stems. Of stems that grow +above ground, the sugar cane probably comes first in economic +importance on this account. In hot, arid regions, where the moisture +drawn from the earth would, during prolonged drought, be too rapidly +dissipated by an expanded surface of leaves, the whole plant, as +in the case of the cactus, is sometimes compacted into a greatly +thickened stem, which fills the triple office of leaf, stalk, and +water reservoir. + +[Illustration: FIG. 104.—Rootstock of creeping panic grass.] + +=104. The uses of underground stems.=—It is in these that the storage +of nourishment most frequently takes place, and the modifications +that stems undergo for this purpose are in some cases so great that +their real nature becomes apparent only after a careful examination. +But while the chief function of underground stems is the storage of +nourishment, they serve other purposes also. In plants requiring a +great deal of moisture, like the ferns, and in others growing in dry +places and needing to husband moisture carefully, like the blackberry +lily, underground stems may be useful in preventing the too rapid +evaporation that would take place through aërial stems. Defense +against frost, cold, heat, and other dangers, as well as quickness of +propagation, are also attained or assisted by this means. + +=105. Rootstocks and rhizomes.=—From a prostrate stem like that +shown in Fig. 95 to a creeping rootstock like the one in Fig. 104, +the transition is so easy that we find no difficulty in accounting +for it. From the prostrate rootstock to the thickened storage +rhizome (Fig. 105) of such plants as the iris, puccoon, bulrush, and +Solomon’s-seal, is a longer step, but the bud with its leaf scales +at the growing tip, _a_, the remains of the flower stem at the node, +_b_, and the roots from the under surface sufficiently indicate its +nature. The peculiar scars from which the Solomon’s-seal takes its +name are caused by the falling away each year of the flowering stem +of the season after its work is done, leaving behind the node of the +underground stem from which it originated. In this way the rhizome +lives on indefinitely, growing and increasing at one end as fast as +it dies at the other. Test a little of the substance of the rhizome +with iodine. Of what does it consist? Of what use is it to the plant? + +[Illustration: FIG. 105.—Rhizome of Solomon’s-seal: _a_, growing bud +at the tip; _b_, remains of the past season’s flower stem; _c_, _c_, +_c_, scars of old stems. (_After_ GRAY.)] + +[Illustration: FIG. 106.—Potato tuber showing lenticels, _A_, _A_, or +pores for air on the surface; _S_, leaf scale, or scar.] + +=106. The tuber.=—A still further thickening and shortening of +the rhizome gives rise to the tuber, of which the potato and the +Jerusalem artichoke are familiar examples. Can you give any evidence +to show that the potato is a modified stem? Find the point of +attachment of the tuber to its stem and stand it on this end, which +is its natural base. Notice that the eye sits in the axil of the +little scale that forms the eyelid. What does the scale represent? +What is the eye? (100.) Do the scales occur in any regular order—that +is, opposite, or alternating with, each other, like the leaves on +a stem? Look on the surface for a number of small, lens-shaped +dots (_A_, _A_, Fig. 106) scattered irregularly over it. These are +aërating pores called _lenticels_, and are found in most dicotyl +stems. Does their presence help to throw light on the real nature +of the tuber? If any sprouts occur on your specimen, where do they +originate? Where do buds and sprouts originate on plants above +ground? Make a sketch of the outside of a potato, showing the +lenticels, eyes, and scales, or the scars left by the scales in case +they have fallen away, as has probably happened, if your specimen is +an old one. + +[Illustration: FIGS. 107, 108.—Transverse and longitudinal sections +of the potato: _A_, skin; _B_, cortical layer; _C_, outer pith layer; +_D_, inner pith layer.] + +Cut a small slice from the stem end of two potatoes, stand them in +coloring fluid for four or five hours, then divide into cross and +vertical sections, as shown in Figs. 107, 108, and draw, labeling the +parts that you can make out. Through which has the liquid ascended +most rapidly? Test with iodine and find out in which part nourishment +is most abundant. It is this abundant store of food that makes +the potato such a valuable crop in cold countries like Norway and +Iceland, where the seasons are too short to admit of the slow process +of developing the plant from the seed. + +[Illustration: FIG. 109.—Scaly bud of oak, enlarged.] + +[Illustration: FIG. 110.—Scaly bulb of lily (GRAY).] + +Compare a common potato with a sweet potato. Are there any eyes or +buds on the latter? Is there a scale below them? Do they occur in any +regular order? Do you see any lenticels? The common potato and the +sweet potato are both tubers; can you give some of the reasons why +the one is regarded as a modified branch, and the other as a root? +(100.) Compare their food contents; which contains most starch? Which +most sugar? How can you judge about the sugar without a chemical test? + +=107. The bulb= is a form of underground stem reduced to a single +bud. Get the scaly bulb of a lily, and sketch it from the outside +and in cross and vertical section. Compare it with the scaly winter +buds of the oak and hickory, or other common deciduous tree. Make an +enlarged sketch of the latter on the same scale as the lily bulb, and +the resemblance will at once become apparent. The scales of the bulb +are, in fact, only thick, fleshy leaves closely packed around a short +axis that has become dilated into a flat disk. From the center of +the disk, which is the terminal node of this transformed stem, rises +the flower stalk, or _scape_, as it is called, of the season. After +blossoming, the scape perishes with its bulb, and their place is +taken by new ones which are developed from the axils of the scales, +thus revealing their leaflike nature. + +[Illustration: FIG. 111.—Leaf of an onion divided lengthwise showing +the base enlarged into the coat of a bulb.] + +That bulbs are only modified buds is further shown by the bulblets +that sometimes appear among the flowers of the onion, and in the leaf +axils of certain lilies. They never develop into branches, but drop +off and grow into new plants just as the subterranean bulbs do. + +The bulbs of the onion and hyacinth are still further modifications, +in which the scales consist of the thickened bases of leafstalks that +are dilated until each one completely envelops the growing parts +within. + +=108. Morphology= is the part of botany that treats of the origin, +form, and uses of the different organs of plants, and of the +modifications they undergo in adapting themselves to changes of +condition or function. Organs or parts that have the same origin +but have become adapted to different functions, like the flattened +stems of the butcher’s-broom or the bulb scales of the lily, are +said to be _homologous_; those that are different in origin but +adapted to the same function, as the sweet and common potatoes, are +_analogous_. In other words, homologous organs are morphologically +alike, but may be physiologically different; analogous organs are +alike physiologically, but differ morphologically. + +=109. Economic value of stems.=—We probably get a greater variety +of economic products from the stem than from any other part of the +plant. Consider the vast amount of food stored in underground stems +like the potato; the resins, gums, and sugar found in the sap of +plants like the sugar cane, the pine, and India-rubber trees; the +medicines, dyes, and extracts obtained from the tissues; the valuable +fibers, such as flax, jute, and hemp, furnished by the bast; the wood +pulp for making paper; and the timber for building and furnishing +our houses that we get from the woody trunks of trees. When we think +of all these things, it seems hardly possible to overestimate the +importance of this part of the vegetable kingdom to man, or to exert +ourselves too strenuously to regulate and prevent the destruction of +these invaluable natural resources. + + + Practical Questions + + 1. Would you judge from the observations made in the foregoing + section, that the work of an organ determines its form, or that the + form determines its work? (99, 100, 108.) + + 2. Which is the more important, form or function? + + 3. Name some plants that are propagated by rootstocks; by runners + or stolons; by rhizomes; by tubers; by bulbs. + + 4. What is the advantage of propagating in this way over planting + the seed? (104, 106.) + + 5. Mention any other advantages that the various plants named may + gain from the development of their underground parts. (104.) + + 6. What makes the nut grass so troublesome to farmers in some parts + of the country? + + 7. Is its “nut” a root or a tuber? How can you tell? (106.) + + 8. Suggest some ways for destroying weeds that are propagated in + this way. + + 9. Could you get rid of wild onions in a pasture by mowing them + down? By digging them up? (107.) + + 10. Is it wise for farmers to neglect the appearance of such a weed + in their neighborhood, even though it does not infest their own + land? + + 11. Name any plants of your neighborhood, either wild or + cultivated, that are valued for their rhizomes; for their tubers. + + 12. What part of the plants named below do we use for food or other + purposes? Ginger, angelica, ginseng, cassava, arrowroot, garlic, + onion, sweet flag, iris, sweet potato, Cuba yam, artichoke. + + 13. Why are the true roots of bulbous and rhizome-bearing plants + generally so much smaller in proportion to the other parts than + those of ordinary plants? (89, 104.) + + 14. If the Canada thistle grows in your vicinity, examine the roots + and see if there is anything about them that will help to account + for its hardihood and persistency. + + 15. If you live in the region of the horse nettle (_Solanum + Carolinense_), explain how it is helped by its root system. (89.) + + + III. STEM STRUCTURE + + + A. MONOCOTYLS + + MATERIAL.—Fresh cornstalks with several well-developed nodes, some + of which should have stood in coloring fluid from 1 to 3 hours. If + fresh specimens cannot be obtained from the fields, a number of + seedlings may be grown in boxes of rich earth and cared for by the + pupils either at home or in the schoolroom; they should be planted + 4 or 5 weeks before needed. Asparagus and smilax sprouts may be + used, or the stem of any large grass, or of wheat and other grains, + but stalks of corn or sugar cane make the best subjects for study + where they can be obtained. + + APPLIANCES.—A compound microscope will be needed for detailed + study. Prepared slides can be used, but it is better for students + to make their own sections where practicable. + +[Illustration: FIG. 112.—Cross section of a cornstalk (reduced): _v_, +fibrovascular bundles; _c_, cortex; _p_, pith.] + +=110. Gross anatomy of a monocotyl stem.=—Obtain a fresh +cornstalk,—preferably one that has begun to tassel,—and observe its +external characters. How are the internodes divided from one another? +What is the use of the very firm, smooth epidermis? Notice a hollow, +grooved channel running down one side between the _joints_, or nodes; +does it occur in all of them? Is it on the same side or on the +opposite sides of alternate internodes? Follow one of these grooves +to the node from which it originates; what do you find there? After +studying the internal structure of the stalk, you will understand why +this groove should occur on the side of an internode bearing a bud or +fruit. + +Cut a cross section midway between two nodes, and observe the +composition of the interior; of what does the bulk of it appear to +consist? Notice the arrangement of the little dots, like the ends of +cut-off threads, that are scattered through the pith; where are they +most abundant, toward the center or the circumference? + +[Illustration: FIG. 113.—Vertical section of cornstalk (reduced): +_g_, groove; _c_, cortex; _v_, fibrovascular bundles mingled with +parenchyma; _b_, bud; _n_, node.] + +Make a vertical section through one of the nodes. Cut a thin slice +of the pith, hold it up to the light, and examine with a hand lens. +Observe that it is composed of a number of oblong cells packed +together like bricks in a wall. These are filled with protoplasm +and cell sap, and constitute what is known to botanists as the +_parenchyma_ or fundamental tissue from which all the other tissues +are derived. Apply the iodine test; in what parts does starch occur +most abundantly? + +Draw out one of the woody threads running through the pith. Break +away a bit of the epidermis, and see how very closely they are packed +on its inner surface. Trace the course of the veins in the bases +of the leaves; find their point of union with the stem; with what +part of it do they appear to be continuous? Has this anything to do +with the greater abundance of fibers near the epidermis? Can you +follow the fibers through the nodes, or do they become confused and +intermixed with other threads there? (If a stalk of sugar cane can be +obtained, the ring of scars left by the vascular bundles as they pass +from the leaves into the stem will be seen beautifully marked just +above the nodes.) + +If there is an eye or bud at the node, see if any of the threads go +into it. Can you account now for the depression that occurs in the +internode above the eye? + +Make drawings of both cross and vertical sections, showing the points +brought out in your examination of the cornstalk. + +=111. The vascular system.=—To find out the use of the threads that +you have been tracing, examine a piece of a living stem that has +stood in red ink for three to twenty-four hours. Notice the course +the coloring fluid has taken; what would you infer from this as to +the use of the woody fibers? + +These threads constitute what is called the _vascular system_ of the +stem, because they are made up of _vessels_ or _ducts_, along which +the sap is conveyed from the roots to the leaves and back from the +leaves to the parts where it is needed after it has contributed to +the elaboration of food. + +On account of this double line of communication which they have to +maintain, the vascular threads, or _bundles_, as they are technically +called, are double; one part composed of larger vessels, carrying +water up, the other consisting of smaller ones, bringing back the +food. Can you give a reason for their difference in size? + +[Illustration: FIG. 114.—Longitudinal section through the stem of a +palm, showing the curved course of the fibrovascular bundles (GRAY, +_after_ FALKENBERG).] + +=112. Woody monocotyls.=—Examine sections of yucca, smilax, or +of palmetto from the handle of a fan, and compare them with your +sketches of the cornstalk. In which are the vascular fibers most +abundant? Which is the toughest and strongest? Why? Trace the course +of the leaf fibers from the point of insertion to the interior. How +does it differ from that of the fibers in a cornstalk? + +=113. Growth of monocotyl stems.=—After tracing the course of the +leaf veins at the nodes of the cornstalk, you will have no difficulty +in identifying these veins as part of the vascular system. In jointed +stems like those of the corn and sugar cane and other grasses, their +intercalation between the vascular bundles of the stem takes place, +as we have seen, at the nodes, forming the hard rings known as +joints; but in other monocotyls the fibers entering the stem from the +leaves usually tend first downward, toward the interior (Fig. 114), +then bend outward, toward the surface, where they become entwined +with others and form the tough, inseparable cortex that gives to +palmetto and bamboo stems their great strength. Generally, monocotyl +stems do not increase in diameter after a certain point, and as +they can contain only a limited number of vascular fibers, they are +incapable of supporting an extended system of leaves and branches. +Hence plants of this class, with a few exceptions, like smilax and +asparagus, are characterized by simple, columnar stems and a limited +spread of leaves. Such plant forms are admirably adapted by their +structure to the purposes of mechanical support. It is a well-known +law of mechanics that a hollow cylinder is a great deal stronger than +the same mass would be in solid form, as may easily be tested by the +simple experiment of breaking in your fingers a cedar pencil and a +joint of cane or a stem of smilax of the same weight. In stems that +may be technically classed as solid in structure, like the corn and +palmetto, the interior is so light compared with the hard epidermis +that the result is practically a hollow cylinder. + +[Illustration: PLATE 4.—Forest of bamboo, showing the tall, straight, +branchless habit of monocotyl stems.] + +=114. Minute study of a monocotyl stem.=—Place under the microscope +a very thin transverse section of a cornstalk. The little dots that +looked like the cut ends of threads to the naked eye will now appear +as the complex group of cells shown in Fig. 115. The same parts are +shown longitudinally in Fig. 116. As seen in cross section, their +arrangement suggests a grotesque resemblance to the face of an old +woman wearing a pair of enormous spectacles and surrounded by a cap +frill of netting with very wide meshes. These are parenchyma cells, +_f_, _f_, Fig. 115, and constitute the greater portion of the living +tissues. + +[Illustration: FIG. 115.—Transverse section through the fibrovascular +bundle of a cornstalk: _a_, annular tracheid; _sp_, spiral tracheid; +_m_ and _m′_, ducts; _l_, air space; _v_, sieve tubes; _s_, companion +cells; _vg_, strengthening fibers; _cp_, bast; _f_, _f_, parenchyma.] + +[Illustration: FIG. 116.—Vertical section of the same; _a_ and _a′_, +rings of a decomposed annular tracheid; _v_, sieve tubes; _s_, +companion cells; _cp_, bast; _l_, air space; _vg_, strengthening +tissue; _sp_, spiral duct.] + +The two large openings, _m_, _m′_, that represent the spectacles, are +ducts for carrying water _up_ the stem. They are called pitted ducts +on account of the bordered pits which cover their outer surface. The +two smaller openings between and slightly below the pitted ducts are +also vessels for carrying liquids up the stem. The lower one, _a_, +is called the annular _tracheid_ because its tube is strengthened +by rings on the inside. The upper, smaller one, _sp_, is known as +the spiral tracheid, because its walls are reinforced by spiral +thickenings. Can you think what is the use of these strengthening +contrivances in the walls of conducting cells? (Suggestion: What is +the use of the spiral wire on a garden hose?) The large, irregular +opening below the ducts is an air space. What is its object? Why has +it no surrounding wall? + +Next look above the ducts for a group of rhomboidal or hexagonal +cells, _v_, _v_, with smaller ones, _s_, between them. The larger of +these are _sieve tubes_, the smaller ones, _companion cells_. The +sieve tubes carry sap _down_ the stem after it has been made into +food by the leaves. They get their name from the sievelike openings +between the connecting walls of the cells which form them—as if a row +of pepper boxes with perforations at both top and bottom were placed +end to end, so as to form a long tube divided into compartments +by perforated walls. Can you give a reason why the cells of ducts +that carry elaborated nutriment should have a more open line of +communication than those carrying crude sap? [56 (2).] Which one of +the organic food substances was shown by Exp. 39 to be unable, or +nearly so, to pass through the cell wall by osmosis? [56 (4).] The +conducting cells are surrounded by a mass of strengthening fibers +separating them from the parenchyma, _f_, and constituting with +them a _fibrovascular bundle_. The larger vessels, _m_, _m′_, _a_, +and _sp_, compose the _xylem_, the harder, more woody part of the +bundle, and the smaller ones, _v_, _s_, the _phloëm_, or softer part. +Notice also that there is no parenchyma in contact with the xylem +and phloëm in the fibrovascular bundles of a monocotyl, to supply +material for new growth, but they are entirely surrounded by a sheath +of strengthening tissue, whence such bundles are said to be _closed_, +and are incapable of further growth by the addition of new cells. + +[Illustration: FIG. 117.—Horizontal view of the sieve tube of a gourd +stem, showing perforations.] + +[Illustration: FIG. 118.—Side view of the sieve tube of a gourd +stem: _pr_, protoplasm layer; _u_, albuminous contents, forming +mucilaginous strand.] + + + B. HERBACEOUS DICOTYLS + + MATERIAL.—Young stems of sunflower, hollyhock, burdock, ragweed, + cocklebur, castor bean, or any large herbaceous plant. In schools + unprovided with compound microscopes, the minute anatomy can be + studied with some degree of profit by the aid of pictures. + +=115. Gross anatomy.=—Examine the outside of a young stem of +sunflower, burdock, or other herbaceous dicotyl. Notice whether it +is smooth, or roughened with hairs, scales, ridges, or grooves. If +hairy, observe the nature of the hairs, whether bristly, downy, +sticky, etc. Notice the color of the epidermis, whether uniform, or +splotched or striped with other colors, as, for example, jimson weed, +and pigweed (amarantus). If there are any buds, branches, or flower +stems, notice where they originate; what is the angle between the +leaf and stem called? (100.) + +Make a transverse cut through a portion of the stem that has stood +for a time in coloring fluid and examine with a lens. Four regions +can easily be distinguished: (1) the epidermis, _e_, Fig. 119; (2) +the primary cortex, _c_; (3) a ring of fibrovascular bundles, _f_; +and (4) a central cylinder of parenchyma, _p_. In some specimens +there will be a fifth region, the pith, which will appear in the +section as a white circular spot in the center of the parenchyma. + +[Illustration: FIG. 119.—Transverse section of a very young stem +of burdock, showing fibrovascular bundles not completely united +into a ring: _e_, epidermis; _c_, primary cortex; _f_, a ring of +fibrovascular bundles; _p_, central cylinder of parenchyma.] + +In specimens a little older than the one shown in Fig. 119, a narrow +circular line will be seen running through the ring of bundles nearly +midway between their inner and outer extremities, connecting them +into an unbroken circle around the central cylinder. This is the +_cambium_ layer, which supplies the vascular region with materials +for new growth, and thus enables dicotyl stems to increase in +diameter by the successive addition of fresh vascular rings from year +to year. + +Examine in the same way a vertical section, and find the parts +corresponding to those shown in Fig. 119. Make enlarged sketches of +both sections, labeling the various parts observed. + +=116. Minute structure of a dicotyl stem.=—Place successively under +a high power of the microscope thin transverse and longitudinal +sections of the stem just examined, or such other specimen as the +teacher may provide. Bring one of the fibrovascular bundles into the +field, and try to make out the parts shown in Figs. 120 and 121. +The corresponding parts in the two sections are indicated by the +same letters. Notice the cortex, _R_, on the outside and the pith, +_M_, on the inside; between these, the cambium, _C_, the _xylem_, +or woody tissue, included between the radiating lines _X_, and the +newer tissues composing the _phloëm_ between the lines _P_. The +cambium and pith, which includes the medullary rays so conspicuous +in perennial stems, are composed of live parenchyma cells, from +which alone growth can take place; they are the active part of the +stem. The xylem contains the large vessels, _t_ and _s_, that convey +water _up_ the stem, together with the wood fibers, _h_. These are +the permanent tissues. After completing their growth the cells of +the xylem gradually lose their protoplasm, and all vitality ceases. +Even the cell sap disappears, and sometimes the walls of the ducts +are disintegrated, leaving a mere air space like that shown at _l_ +in Figs. 115 and 116. The dead cells and tissues, however, are by +no means useless. They constitute the heartwood that is so valuable +for timber, and serve an important purpose as a mechanical support +for the stem. The phloëm contains on its outer face a mass of hard +fibers, _b_, called bast, and toward the interior, the sieve tubes, +_sb_, with a number of smaller vessels that convey _down_ the stem +the sap containing the food made in the leaves. It is separated from +the cortex by the bundle sheath, _e_, and on its other side, from +the exterior face of the xylem by the cambium, _C_. In this position +the growing cambium adds new cells to the inner side of the phloëm, +and to the outer side of the xylem, so that the former grows on its +inner face and the latter on its outer. In perennial plants, as new +rings are added to the xylem from season to season, the older ones +die and are changed into heartwood, which thus gradually increases in +thickness till in some of the giant redwoods and eucalypti, it may +attain a diameter of thirty-five or forty feet. In the phloëm, on +the other hand, as new cells are added from within, the older ones +are gradually changed into hard bast, _b_, then into bark, and are +finally sloughed off and fall to the ground. It is this free line of +communication with the active cambium that enables dicotyl stems to +grow on indefinitely, the sheath, _e_, being formed on the exterior +face of the bundles only, leaving the other free, whence they are +said to be _open_. + +[Illustration: FIGS. 120-121.—Transverse and longitudinal sections of +a fibrovascular bundle in the stem of a sunflower. The two sections +are lettered to correspond: _M_, pith (parenchyma); _X_, xylem +region; _P_, phloëm; _R_, cortex; _s_, spiral ducts; _s′_, annular +ducts; _t_, _t_, pitted ducts; _C_, cambium between the phloëm and +xylem regions; _sb_, sieve tubes; _b_, bast; _e_, bundle sheath; +_ic_, cambium (parenchyma) cells; _h_, wood fibers.] + +Make drawings of cross and vertical sections of a dicotyl stem as +it appears under the microscope, labeling correctly all the parts +observed. Show the shape and relative size of the different cells. +Compare your drawings with those made in your study of monocotyl +stems, and write in your notebook the essential points of difference +between the two. + +[Illustration: FIG. 122.—Internal structure of a pine stem, showing +longitudinal section of a fibrovascular bundle through a medullary +ray, _sm_, _sm′_; _s_, tracheids; _t_, bordered pits, surface view; +_c_, cambium; _v_, sieve tubes; _vt_, sieve pits, analogous to the +sieve plates in dicotyl stems.] + +[Illustration: FIG. 123.—Internal structure of a pine stem, showing +transverse section of a tracheid: _i_, cell walls; _m_, intermediate +layer between walls of adjoining cells; _m′_, intercellular space +here occupied by substance of intermediate layer; _b_, bordered pit +in section at right angles to the surface; _t_, membrane for closing +the pit canal.] + +=117. The stems of conifers=, the group of Gymnosperms to which the +pine belongs, do not differ greatly from those of dicotyls, the +chief difference being that the vascular bundles contain tracheids +only, corresponding to the smaller vessels of the phloëm, _s_ and +_s′_, shown in Fig. 121. These tracheids have large sunken places in +their walls, called bordered pits (Fig. 123), closed by a very thin +membrane through which water and dissolved food materials can more +readily percolate. In all other essentials, the internal structure of +pine stems is like that of dicotyls. (See Plate 5.) + + + C. WOODY STEMMED DICOTYL + + MATERIAL.—Elm, basswood, mulberry, leatherwood, and pawpaw show the + bast well; sassafras, slippery elm, and (in spring) hickory and + willow show the cambium; grape and trumpet vine, the ducts. Some + of the specimens used should be placed in coloring fluid from 3 to + 8 hours before the lesson begins. The rate at which the liquid is + absorbed varies with the kind of stem and the season. It is more + rapid in spring and slower in winter. If a cutting stands too long + in the fluid, the dye will gradually percolate through all parts of + it; care should be taken to guard against this. + +[Illustration: FIG. 124.—Part of a young China tree shoot, showing, +_A_, lenticels; _B_, leaf scar; _C_, _C_, traces left by the broken +ends of fibrovascular bundles that passed from the stem into the +leaf. Natural size.] + +=118. The external layer.=—While the primary structures, as shown +in the last section, are essentially the same in all dicotyl stems, +the continued yearly growth of perennials causes them to develop +a number of secondary structures and variations of detail that +differentiate them in a marked degree from soft-stemmed annuals. Take +a piece of a three-year-old shoot of cherry, horse chestnut, or any +convenient hardwood tree, and notice that the soft, green epidermis +has given place to a thicker, harder, and usually darker colored +bark. Notice the presence of lenticels (106) and their porous, corky +texture for the admission of air to the interior. They are slightly +raised above the surface of the bark, and are usually round, or more +or less elongated in different directions, according as they are +stretched vertically or horizontally by the growth of the axis. The +characteristic markings of birch bark, which make it so ornamental, +are due to the lenticels. In most trees they disappear on the older +parts, where the bark is constantly breaking away and sloughing off. + +[Illustration: PLATE 5.—Stem of a conifer, _Sequoia gigantea_, +Mariposa Grove, California. The first branch, 6 feet in diameter, +leaves the parent trunk 125 feet above the ground. The photographer +sitting on one of the exposed roots affords a good standard for +comparison. The tree is noted for its massive limbs. The smaller +trees in the background show the characteristic mode of branching in +trees of this class.] + +=119. Internal structures.=—Cut a transverse section through your +specimen, and notice under the epidermis a greenish layer of young +bark; beneath this a layer of rather tough, stringy bast fibers, and +beyond these a harder woody substance that constitutes the bulk of +the interior; within this, at the very center of the axis, we find +a cylinder of lighter texture, the pith, or medulla, occupying the +place of the soft parenchyma which fills this space in very young +stems. + +Between the woody axis and the bark notice a more or less soft and +juicy ring. + +=120. The cambium layer.=—This is not always easily distinguishable +with a hand lens, but is conspicuous in the stems of sassafras, +slippery elm, and aristolochia. If some of these cannot be obtained, +the presence of the cambium can be recognized by observing the +tendency of most stems to “bleed,” when cut, between the wood and +bark. The reason for this is because the cambium is the active part +of the stem, in which growth is taking place, and consequently it is +most abundantly supplied with sap. In spring, especially, it becomes +so full of sap that if a rod of hickory or elder is pounded, the +pulpy cambium is broken up and the bark may be slipped off whole from +the wood. + +=121. Medullary rays.=—Observe the whitish, silvery lines that +radiate in every direction from the center, like the spokes of a +wheel from the hub. These are the medullary rays, and consist of +threads of pith that serve as lines of communication between the +“central cylinder” and the growing cambium layer. In old stems the +central pith frequently disappears and its office is filled by the +medullary rays, which become quite conspicuous. + +[Illustration: FIGS. 125, 126.—Cross sections of twigs: 125, section +across a young twig of box elder, showing the four stem regions: _e_, +epidermis, represented by the heavy bounding line; _c_, cortex; _w_, +vascular cylinder; _p_, pith; 126, section across a twig of box elder +three years old, showing three annual growth rings, in the vascular +cylinder. The radiating lines (_m_), which cross the vascular region +(_w_), represent the pith rays, the principal ones extending from the +pith to the cortex (_c_). (_From_ COULTER’S “Plant Relations.”)] + +=122. Structural regions of a woody stem.=—Sketch cross and vertical +sections of your specimen, as seen under the lens, labeling the +different parts. Refer to Figs. 125, 126, if you have any difficulty +in distinguishing the parts. In a year-old shoot (Fig. 125), the +structural regions correspond closely to those shown in Fig. 119, +except that the ring of fibrovascular bundles is here compact and +woody, and crossed by the radiating lines of the medullary rays. In +a three-year-old shoot (Fig. 126), the main divisions are the same, +but the soft parenchyma of the central cylinder is replaced by the +pith, and the vascular ring is composed of three layers corresponding +to the three years of growth. In general, mature dicotyl stems may be +said to include four well-defined regions: (1) the epidermis, or the +bark; (2) the cortex, made up of bast and certain other tissues; (3) +the cambium; (4) the woody vascular cylinder, made up of concentric +rings, each representing a year’s growth. The pith, or medulla, +constitutes a fifth region, but is obvious only in young stems. +Notice the little pores or cavities that dot the woody part in the +cross section; where are they largest and most abundant? How are the +rings marked off from one another? These pores are the sections of +ducts. They are very large in the grapevine, and a cutting two or +three years old will show them distinctly. Examine sections of a twig +that has stood in red ink from three to twelve hours, and observe +the course the fluid has taken. How does this accord with the facts +observed in your study of the conducting tissues in monocotyl and +herbaceous stems? (111, 115, 116.) + +[Illustration: FIG. 127.—Diagram illustrating the annual growth of +dicotyledons.] + +=123. The rings= into which the woody cylinder is divided mark the +yearly additions to the growth of the stem, which increases by the +constant accession of new material to the outside of the permanent +tissues (116). The cambium constantly advances outward, beginning +every spring a new season’s growth, and leaving behind the ring of +ducts and woody fibers made the year before. As the work of the plant +is most active and its growth most vigorous in spring, the largest +ducts are formed then, the tissue becoming closer and finer as the +season advances, thus causing the division into annual rings that is +so characteristic of woody dicotyl stems. Each new stratum of growth +is made up of the fibrovascular bundles that supply the leaves and +buds and branches of the season. In this way we see that the increase +of dicotyl trunks and branches is approximately in an elongated cone +(Fig. 127), the number of rings gradually diminishing toward the top +till at the terminal bud of each bough it is reduced to a single one, +as in the stems of annuals. + +Sometimes a late autumn, succeeding a very dry summer, will cause +trees to take on a second growth, and thus form two layers of wood +in a single season. On this account we cannot always rely absolutely +upon the number of rings in estimating the age of a tree, though the +method is sufficiently exact for all practical purposes. + + + Practical Questions + + 1. Old Fort Moultrie near Charleston was built originally of + palmetto logs; was this good engineering or not? Why? (113.) + + 2. Explain the advantages of structure in a culm of wheat; a stalk + of corn; a reed. (113.) + + 3. Would the same quality be of advantage to an oak? Why, or why + not? + + 4. Is it of any advantage to the farmer that grain straw is so + light? + + 5. Explain why boys can slip the bark from certain kinds of wood in + spring to make whistles. (120.) + + 6. Why cannot they do this in autumn or winter? (123.) + + 7. Name some of the plants commonly used for this purpose. + + 8. Is the spring, after the buds begin to swell, a good time to + prune fruit trees and hedges? (120.) + + 9. What is the best time, and why? + + 10. Why are grapevines liable to bleed to death if pruned too late + in spring? (120, 123.) + + 11. Why are nurserymen, in grafting, so careful to make the cambium + layer of the graft hit that of the stock? (120.) + + 12. In calculating the age of a tree or bough from the rings of + annual growth, should we take a section from near the tip, or from + the base? Why? (123.) + + + IV. THE WORK OF STEMS + + MATERIAL.—Leafy shoots of grape, balsam, peach, or other active + young stems; a cutting of willow, currant, or any kind of easily + rooting stem. Two bottles of water and some linseed or cottonseed + oil. + +[Illustration: FIG. 128.—Experiment showing that moisture is thrown +off by the leaves of plants.] + + EXPERIMENT 58. DO THE LEAVES HAVE ANY ACTIVE PART IN EFFECTING THE + MOVEMENT OF SAP IN THE STEM?—Take two healthy young shoots of the + same kind—grape, peach, corn, tropæolum, calla lily absorb rapidly. + Trim the leaves from one shoot and close the cut surfaces with + a little vaseline or gardener’s wax to prevent loss of water by + evaporation. Place the lower end of each in a glass jar or tumbler + filled to the same height with water. Cut off _under water_ a + half inch from the bottom of each shoot, to get a fresh absorbing + surface. This is necessary because exposure to air for even a + second greatly hinders absorption by permitting the entrance of air + into the severed ends of the ducts. Pour a little oil on the water + in both jars to prevent evaporation. (Do not use kerosene; it is + injurious to plants.) At the end of twenty-four hours, which vessel + has lost the more water? How do you account for the difference? + + EXPERIMENT 59. WHAT BECOMES OF THE WATER THAT GOES INTO THE + LEAVES?—Cover the top of the vessel containing the leafy twig used + in the last experiment with a piece of cardboard, having first + cut a slit in one side, as shown in Fig. 128, so that it can be + slid into place without injuring the stem. Invert over the twig a + tumbler that has first been thoroughly dried, and leave in a warm, + dry place. After an hour or two, what do you see on the _inside_ of + the tumbler? Where did the moisture come from? + +[Illustration: FIG. 129.—A twig which had been kept standing in water +after the removal of a ring of cortical tissue: _a_, level of the +water; _b_, swelling formed at the upper denudation; _c_, roots.] + + EXPERIMENT 60. THROUGH WHAT PART OF THE STEM DOES THE SAP FLOW + UPWARD?—Remove a ring of the cortical layer from a twig of any + readily rooting dicotyl, such as willow, being careful to leave the + woody part, with the cambium, intact. Place the end _below_ the cut + ring in water, as shown in Fig. 129. The leaves above the girdle + will remain fresh. How is the water carried to them? How does this + agree with the movement of red ink observed in 115 and 122? + + EXPERIMENT 61. THROUGH WHAT PART DOES THE SAP COME DOWN?—Next prune + away the leaves and protect the girdled surface with tin foil, or + insert it below the neck of a deep bottle to prevent evaporation, + and wait until roots develop. Do they come more abundantly from + above or below the decorticated ring? + +=124. The three principal functions of the stem= are:—(1) to serve +as a mechanical support and framework for binding the other organs +together and bringing them into the best attainable relations with +light and air; (2) as a water carrier, or pipe line, for conveying +the sap from the roots to the parts where it is needed; and (3) as a +receptacle for the storage of foods. + +=125. Movement of water.=—It has already been shown (71, 111) that +a constant interchange of liquid is taking place through the stem, +between the roots, where it is absorbed from the ground, and the +leaves, where it is used partly in the manufacture of food. Just +what causes the rise of sap in the stem is one of the problems of +vegetable physiology that botanists have not yet been able to solve. +There are, however, certain forces at work in the plant, which, +though they may not account for all the phenomena of the movement, +undoubtedly influence them to a great extent. From experiments 58-61, +we can obtain an idea of what some of these forces may be. + +[Illustration: FIG. 130.—The stump of a large oak that was injured by +lightning many years ago. The interior is completely decayed, leaving +only a hollow shell of living tissue, from which branches continue to +put forth leaves year after year.] + +=126. Direction of the current.=—These experiments show that the +upward movement of crude sap toward the leaves is mainly through the +ducts in the woody portion of the stem, while the downward flow of +elaborated sap from the leaves takes place chiefly through the soft +bast and certain other vessels of the cortical layer. The action of +the leaves in giving off part of the water absorbed, as shown in Exp. +59, probably has also an important influence on the course of sap +movement. If loss of water takes place in any organ through growth or +other cause, the osmotic flow of the thinner sap from the roots will +set in that direction. + +=127. Ringing fruit trees.=—The course of the sap explains why +farmers sometimes hasten the ripening of fruit by the practice of +_ringing_. As the food material cannot pass below the denuded ring, +the parts above become gorged, and a process of forcing takes place. +The practice, however, is not to be commended, except in rare cases, +as it generally leads to the death of the ringed stem. The portion +below the ring can receive no nourishment from above, and will +gradually be so starved that it cannot even act as a carrier of crude +sap to the leaves, and so the whole bough will perish. + +[Illustration: FIG. 131.—Diagram showing general movement of sap.] + +=128. Sap movement not circulation.=—It must not be supposed that +this flow of sap in plants is analogous to the circulation of the +blood in animals, though frequently spoken of in popular language +as the “circulation of the sap.” There is no central organ like the +heart to regulate its flow, and the water taken up by the roots does +not make a continual circuit of the plant body as the blood does of +ours, but is dispersed by a process of general diffusion, partly into +the air through the leaves and partly through the plant body as food, +wherever it is needed. Figure 131 gives a good general idea of the +movement of sap in trees, the arrows indicating the direction of the +movement of the different substances. + +=129. Unexplained phenomena.=—Though the forces named above +undoubtedly exert a powerful influence over sap movement, their +combined action has not been proved capable of lifting the current +to a height of more than 200 feet, while in the giant redwoods of +California and the towering blue gums of Australia, it is known to +reach a height of more than 400 feet. The active force exerted by the +cell protoplasm has been suggested as an efficient cause, but as the +upward flow takes place through the cells of the xylem, which contain +no protoplasm (116), this explanation is inadequate, and we must be +content, in the present state of our knowledge, to accept the fact as +one which science has yet to account for. + + + Practical Questions + + 1. Why will a leafy shoot heal more quickly than a bare one? (125, + 126; Exp. 58.) + + 2. Why does a transverse cut heal more slowly than a vertical one? + (126, 127.) + + 3. Why does a ragged cut heal less rapidly than a smooth one? + + 4. Why does the formation of wood proceed more rapidly as the + amount of water given off by the leaves is increased? (126; Exp. + 59.) + + 5. Why do nurserymen sometimes split the cortex of young trees in + summer to promote the formation of wood? (116, 118.) + + 6. What is the advantage of scraping the stems of trees? + + 7. Explain the frothy exudation that often appears at the cut ends + of firewood, and the singing noise that accompanies it. [120, 124 + (2).] + + 8. Of what advantage is it to high climbing plants, like grape and + trumpet vine (_Tecoma_), to have such large ducts? (111, 116, 122.) + + 9. Why is the process of layering more apt to be successful if the + shoot is bent or twisted at the point where it is desired to make + it root? (127; Exps. 60, 61.) + + 10. Why do oranges become dry and spongy if allowed to hang on the + tree too long? (72, 126; Exps. 60, 61.) + + 11. Why will corn and fodder be richer in nourishment if, at + harvest, the whole stalk is cut down and both fodder and grain are + allowed to mature upon it? (126, 127; Exps. 60, 61.) + + 12. Is the injury done to plants by freezing due, as a general + thing, to mechanical, or to chemical action? (33.) + + 13. Why in pruning a branch is it best to make the cut just above a + bud? (Exps. 60, 61.) + + 14. Why is the rim of new bark, or callus, that forms on the upper + side of a horizontal wound, thicker than that on the lower side? + (126, 127; Exps. 60, 61.) + + 15. Why is it that the medicinal or other special properties of + plants are found mostly in the leaves and bark, or in the parts + immediately under the bark? (120, 126.) + + 16. Why does twisting the footstalk of a bunch of grapes, just + before ripening, make them sweeter? (127.) + +[Illustration: PLATE 6.—A white oak, one of the monarchs of the +dicotyl type. The owner of the ground on which this noble tree stands +left a clause in his will bequeathing it in perpetuity a territory +of 8 feet in every direction from its base. Refer to 89 and decide +whether such an amount of standing room is sufficient to secure the +preservation of this beautiful object.] + + 17. Is it a mere superstition to drive nails into the stems of plum + and peach trees to make them bear larger or more abundant fruit? + (126, 127.) + + 18. Why is a living corn stalk heavier than a dry one? (124.) + + 19. Why is a stalk of sugar cane heavier than one of corn? + Suggestion: Which is the heavier, pure water, or water holding + solids in solution? + + + V. WOOD STRUCTURE IN ITS RELATION TO INDUSTRIAL USES + + MATERIAL.—Select from the billets of wood cut for the fire, sticks + of various kinds; hickory, ash, oak, chestnut, maple, walnut, + cherry, pine, cedar, tulip tree, all make good specimens. Red + oak shows the medullary rays well. Get sticks of green wood, if + possible, and have them planed smooth at the ends. Collect also, + where they can be obtained, waste bits of dressed lumber from a + carpenter or joiner. If nothing better is available, any pieces of + unpainted woodwork about the schoolroom will furnish subjects for + study. + +=130. Detailed structure of a woody stem.=—Select a good-sized billet +of hard wood, and count the rings of annual growth. How old was the +tree or the bough from which it was taken? Was its growth uniform +from year to year? How do you know? Are the rings broader, as a +general thing, toward the center or the circumference? How do you +account for this? Is each separate ring of uniform thickness all the +way round? Mention some of the circumstances that might cause a tree +to grow less on one side than on the other. Are the rings of the same +thickness in all kinds of wood? Which are the more rapid growers, +those with broad or with narrow rings? Do you notice any difference +in the texture of the wood in rapid and in slow growing trees? Which +makes the better timber as a general thing, and why? + +=131. Heartwood and sapwood.=—Notice that in some of your older +specimens (cedar, black walnut, barberry, black locust, chestnut, +oak, Osage orange, show the difference distinctly) the central part +is different in color and texture from the rest. This is because +the sap gradually abandons the center (116, 123) to feed the outer +layers, where growth in dicotyls takes place; hence, the outer +part of the stem usually consists of sapwood, which is soft and +worthless as timber, while the dead interior forms the durable +heartwood so prized by lumbermen. The heartwood is useful to the +plant principally in giving strength and firmness to the axis. It +will now be seen why girdling a stem,—that is, chipping off a ring of +the softer parts all round, will kill it, while vigorous and healthy +trees are often seen with the center of the trunk entirely hollow. + +[Illustration: FIG. 132.—Cross section through a black oak, showing +heartwood and sapwood. (_From_ PINCHOT, U. S. Dept. of Agr.)] + +[Illustration: FIG. 133.—Vertical section through a black oak. +(_From_ PINCHOT, U. S. Dept. of Agr.)] + +[Illustration: FIGS. 134-136.—Diagrams of sections of timber: 134, +cross section; 135, radial; 136, tangential. (_From_ PINCHOT, U. S. +Dept. of Agr.)] + +=132. Different ways of cutting.=—In studying the vertical +arrangement of stems, two sections are necessary, a radial and a +tangential one. The former passes along the axis, splitting the stem +into halves (Fig. 135); the latter cuts between the axis and the +perimeter, splitting off a segment from one side (Fig. 136). The +appearance of the wood used in carpentry and joiner’s work is due +largely to the manner in which the planks are cut. + +=133. The cross cut.=—The section seen at the end of a log (Figs. +132, 134) is called by carpenters a cross cut. It passes at +right angles to the grain of the wood, and severs what important +structures? (116, 119, 122.) Examine a cross cut at the end of a +rough plank, or the top of a stump or an old fence post, and tell why +this kind of cut is seldom used in carpentry. + +[Illustration: FIG. 137.—Tangential section of mountain ash, showing +ends of the medullary rays.] + +=134. The tangent cut= is so called because it is made at right +angles to the radius of a log. Repeat the geometrical principle upon +which such a cut is described as “tangential.” It passes through +the medullary rays and the annual rings diagonally (Fig. 136), and +is the cheapest way of cutting timber, since the entire log is made +into planks and there is no waste except the “slabs” and “edgings,” +as shown in Fig. 138. The cut ends of the medullary rays appear on +the surface as small lines or slits (Fig. 137), and give to this kind +of plank its peculiar graining. The wavy or “watered” appearance of +the annual rings (Figs. 133, 136, 140, 141), so often seen in cheap +furniture and in the woodwork of cheaply constructed houses, is +caused by the tangential cut, which strikes them at various angles. + +[Illustration: FIG. 138.—Diagram to show the common method of sawing +a log. The circles represent rings of annual growth: _R_, _R_, +diameter of the log; _r_, _r_, _r_ and _t_, _t_, _t_, boards cut +perpendicular to it, giving for the two or three central ones radial, +for the others, tangential, cuts. The waste portions are the “slabs” +and “edgings,” shown in the dark segments at _R_, _R_, and the small +triangular blocks, _e_, _e_, _e_.] + +[Illustration: FIG. 139.—Diagram illustrating the “quartered” cut: +_d_, _d_ and _d′_, _d′_, radial cuts (diameters) by which the log is +“quartered”; _c_, center of the log; _r_, _r_, radii passing through +the middle of each quarter, parallel to which the planks _t_, _t_, +_t_ are cut. The circles represent rings of annual growth.] + +=135. The radial, or quartered cut=, familiar to most of us in the +“quartered oak” of commerce, passes through the center of the log +and cuts the rings of annual growth perpendicularly, giving it the +“striped” appearance (Fig. 135) seen in the best woodwork. It gets +its name from the practice of dealers in first sawing a log into +quarters and then cutting parallel to the radius passing through the +middle of each quarter, as shown in Fig. 139. In this way each cut +strikes the rings perpendicularly, but except in the case of very +large logs, only narrow planks can be obtained in this manner. A +better way of treating small logs is shown in Fig. 138, where the +three central planks, _r_, _r_, _r_, on and near the diameter, will +give the “quartered” effect, while the rest can be used for the +cheaper tangential cuttings. Examine a piece of quartered board, or a +log of wood that has been split down the center, and notice that the +medullary rays appear as silvery bands or plates (Figs. 140, 141). +This is because the cut runs parallel to them. It is the medullary +rays chiefly that give to commercial woods their characteristic +graining. Knots, buds, and other adventitious causes also influence +it in various degrees. + +[Illustration: FIG. 140.—Sections of sycamore wood: _a_, tangential; +_b_, radial; _c_, cross. (_From_ PINCHOT, U. S. Dept. of Agr.)] + +[Illustration: FIG. 141.—Section of white pine wood. (_From_ PINCHOT, +U. S. Dept. of Agr.)] + +[Illustration: FIG. 142.—Section of tree trunk showing knot.] + +=136. The swelling and shrinking of timber.=—The capacity possessed +by certain substances of bringing about an increase of volume by +the absorption of liquids is termed _imbibition_. Care must be +taken not to confound imbibition with capillarity. (Exp. 53.) When +liquids are carried into a body by capillary attraction, they merely +fill up vacant spaces already existing between small particles of +the substance, and therefore do not cause any swelling or increase +in size. When imbibition takes place, the _molecules_, or chemical +units of the liquid, force their way between those of the imbibing +substance, and thus, in making room for themselves, bring about an +increase in volume of the imbibing body. To this cause is due the +alternate swelling and shrinking of timber in wet and dry weather. + +[Illustration: FIGS. 143-144.—Diagrams of tree trunks, showing knots +of different ages: 143, from tree grown in the open; 144, from tree +grown in a dense forest.] + +=137. Knots.=—Look for a billet with a knot in it. Notice how the +rings of growth are disturbed and displaced in its neighborhood. +If the knot is a large one, it will itself have rings of growth. +Count them, and tell what its age was when it ceased to grow. Notice +where it originates. Count the rings from its point of origin to the +center of the stem. How old was the tree when the knot began to form? +Count the rings from the origin of the knot to the circumference +of the stem; how many years has the tree lived since the knot was +formed? Does this agree with the age of the knot as deduced from its +own rings? As the tree may continue to live and grow indefinitely +after the bough which formed the knot died or was cut away, there +will probably be no correspondence between the two sets of rings, +especially in the case of old knots that have been covered up and +embedded in the wood. The longer a dead branch remains on a tree the +more rings of growth will form around it before covering it up, and +the greater will be the disturbance caused by it. Hence, timber trees +should be pruned while very young, and the parts removed should be +cut as close as possible to the main branch or trunk. Sometimes knots +injure lumber very much by falling out and leaving the holes that are +often seen in pine boards. In other cases, however, when the knots +are very small, the irregular markings caused by them add greatly to +the beauty of the wood. The peculiar marking of bird’s-eye maple is +caused by abortive buds buried in the wood. + + + Practical Questions + + 1. Is the swelling of wood a physical or a physiological process? + + 2. Does wood swell equally with the grain and across it? + (Suggestion: test by keeping a block under water for 10 to 20 days, + measuring its dimensions before and after immersion.) + + 3. In building a fence, what is the use of “capping” the posts? + (133.) + + 4. In laying shingles, why are they made to touch, if the work is + done in wet weather, and placed somewhat apart, if in dry weather? + (136.) + + 5. What is the difference between timber and lumber? Between a + plank and a board? Between a log, stick, block, and billet? + + 6. Why does sapwood decay more quickly than heartwood? (131.) + + 7. Explain the difference between osmosis, diffusion, capillarity, + and imbibition. (9, 56, 57, 136; Exp. 53.) + + + VI. FORESTRY + +=138. Practical bearings.=—This part of our subject is closely +related to lumbering and forestry. The business of the lumberman is +to manufacture growing trees into merchantable timber, and to do this +successfully he must understand enough about the structure of wood +to cut his boards to the best advantage, both for economy and for +bringing out the grain so as to produce the most desirable effects +for ornamental purposes. + +[Illustration: PLATE 7.—Timber tree spoiled by standing too much +alone in early youth. Notice how the crowded young timber in the +background is righting itself, the lower branches dying off early +from overshading, leaving tall, straight, clean boles. (_From_ +PINCHOT, U. S. Dept. of Agr.)] + +[Illustration: FIG. 145.—After the forest fire.] + +=139. Forestry has for its object=: (1) the preservation and +cultivation of existing forests; (2) the planting of new ones, or +the reforestation of tracts from which the timber has been destroyed. +Forests may be either _pure_, that is, composed mainly of one kind of +tree, as a pine or a fir wood; or _mixed_, being made up of a variety +of different growths, as are most of our common hardwood forests. + +[Illustration: FIG. 146.—Oyster fungus on linden.] + +=140. Enemies of the forest.=-The first step in the preservation of +our forests is to know the dangers to be guarded against. The chief +of these are: (1) fires; (2) the ignorance or recklessness of man in +cutting for commercial purposes; (3) fungi; (4) injurious insects; +(5) sheep, hogs, and other animals that eat the seeds and the young, +tender growth. + +=141. How to protect the forests.=—The annual destruction of forests +by fires probably exceeds that from all other causes combined. The +only effectual safeguard against this danger is watchfulness on the +part of _everybody_. We can each one of us help in this work by at +least being careful ourselves never to kindle a fire in the woods +without taking every precaution against its spreading. A single +match, or the glowing stump of a cigar, carelessly thrown among dry +leaves or grass, may start a conflagration that will destroy millions +of dollars’ worth of standing timber. + +To prevent the spread of fungi, dead trees should be removed, and +broken or decayed branches trimmed off and the cut surfaces painted. +Birds which destroy insects should be protected; sheep and hogs +should be kept out, and dead leaves left on the ground to cover the +roots and fertilize the soil with the humus created by their decay. +Finally, none but mature trees should be cut for industrial purposes, +and the cutting ought to be done in such a way that the young +surrounding growth will not be injured by the falling trunks. + +=142. The usefulness of forests.=—Aside from the value of their +products, forests are useful in many other ways. They influence +climate beneficially by acting as windbreaks, by giving off moisture +(Exp. 58), by shading the soil, and thus preventing too rapid +evaporation. Their roots also help to retain the water in the soil, +and by this means tend to prevent the washing of the land by heavy +rains and to restrain the violence of freshets. + +=143. Forests and water supply.=—It is especially important that +the watershed of any region should be well protected by forests, +to prevent contamination of the streams and to insure an unfailing +supply of water by checking the escape of the rainfall from the soil. + + + Practical Questions + + 1. Explain the difference between a forest, grove, copse, wood, + woodland. + + 2. In pruning a tree why ought the branch to be cut as close to the + stock as possible? (137.) + + 3. Name the principal timber trees of your neighborhood. What gives + to each its special value? + + 4. Name six trees that produce timber valuable for ornament; for + toughness and strength. + + 5. Which is the better for timber, a tree grown in the open, or one + grown in a forest, and why? (Plate 7.) + + 6. What are the objects to be attained in pruning timber trees? + Orchard and ornamental trees? + + 7. Is the outer bark of any use to a tree, and if so, what? + + 8. Why should pruning not be done in wet weather? [140 (3), 141.] + + 9. Why should vertical shoots be cut off obliquely? [133, 140 (3), + 141.] + + + Field Work + + (1) Make a study of the various climbing plants of your + neighborhood with reference to their modes of ascent, and the + effect, injurious, or other, upon the plants to which they attach + themselves. Note the origin and position of tendrils, and try to + make out what modification has taken place in each case. Consider + the twining habit in reference to parasitism, especially in the + case of soft-stemmed twiners when brought into contact with + soft-stemmed annuals. Observe the various habits of stem growth: + prostrate, declined, ascending, etc., and decide what adaptation to + circumstances may have influenced each case. + + (2) Notice the shape of the different stems met with, and learn + to recognize the forms peculiar to certain of the great families. + Observe the various appliances for defense and protection with + which they are provided, and try to find out the meaning of the + numerous grooves, ridges, hairs, prickles, and secretions that are + found on stems. Always be on the alert for modifications, and learn + to recognize a stem under any disguise, whether thorn, tendril, + foliage, water holder, rootstock, or tuber. + + (3) Note the color and texture of the bark of the different trees + you see and learn to distinguish the most important kinds: + + (_a_) scaly—peeling off annually in large plates, as sycamore, + shagbark-hickory; + + (_b_) fibrous—detached in stiff threads and fibers, as grape; + + (_c_) fissured—split into large, irregular cracks by the growth + of the stem in thickness, as oak, chestnut, and most of our large + forest trees; + + (_d_) membranous—separating in dry films and ribbons, as common + birch (_Betula alba_). + + Observe the difference in texture and appearance of the bark on + old and young boughs of the same species. Try to account for the + varying thickness of the bark on different trees and on different + parts of the same tree. Notice the difference in the timber of + the same species when grown in different soils, at different ages + of the tree, and in healthy and weakly specimens. Find examples + of self-pruning trees (Plate 7), and explain how the pruning was + brought about. + + (4) Select a small plot, about a fourth of an acre, of any wooded + tract in your neighborhood, and make a study of all the trees and + shrubs it contains. Make a list of the different kinds, with the + number of each. Take note of those that show themselves, by vigor + and abundance of growth, best adapted to the situation. These are + the “climax” or dominant vegetation of the plot. Find out, if you + can, to what cause their superiority is due. + +[Illustration: PLATE 8.—The American elm—a perfect type of +deliquescent branching.] + + + + +CHAPTER V. BUDS AND BRANCHES + + + I. MODES OF BRANCHING + + MATERIAL.—For determinate growth, have twigs of an alternate and + an opposite-leaved plant showing well-developed terminal buds: + hickory, sweet gum, cottonwood, poplar, chestnut, are good examples + of the first; maple, ash, horse-chestnut, viburnum, of the second; + for the two-forked kind, mistletoe, buckeye, horse-chestnut, jimson + weed, lilac. For showing indefinite growth: rose, willow, sumach, + and ailanthus are good examples. Gummy buds, like horse-chestnut + and poplar, should be soaked in warm water before dissecting, to + soften the gum; the same treatment may be applied when the scales + are too brittle to be handled without breaking. Buds with heavy fur + on the scales cannot very well be studied in section; the parts + must be taken out and examined separately. + +[Illustration: FIG. 147.—Diagram of excurrent growth.] + +[Illustration: FIG. 148.—Diagram of deliquescent growth.] + +=144. Modes of branching.=—Compare the arrangement of the boughs +on a pine, cedar, magnolia, etc., with those of the elm, maple, +apple, or any of our common deciduous trees. Draw a diagram of each, +showing the two modes of growth. The first represents the _excurrent_ +kind, from the Latin _excurrere_, to run out; the second, in which +the trunk seems to divide at a certain point and flow away, losing +itself in the branches, is called _deliquescent_, from the Latin +_deliquescere_, to melt or flow away. The great majority of stems, +as a little observation will show, present a combination of the two +modes. + +[Illustration: FIG. 149.—Winter twig of sugar maple: _t_, terminal +bud; _ax_, axillary buds; _ls_, leaf scars; _tr_, leaf traces; _l_, +lenticels; _rs_, ring of scars left by bud scales of preceding +season.] + +=145. Terminal and axillary buds.=—Notice the large bud at the end of +a twig of hickory, sweet gum, beech, cottonwood, etc. This is called +the _terminal_ bud because it terminates its branch. Notice the +scars left by the leaves of the season as they fell away, and look +for small buds just above them. These are _lateral_, or _axillary_, +buds, so called because they spring from the axils of the leaves. How +many leaves did your twig bear? What difference in size do you notice +between the terminal and lateral buds? + +=146. The leaf scars.=—Examine the leaf scars with a hand lens, +and observe the number and position of the little dots in them. +Ailanthus, varnish tree, sumach, and China tree show these very +distinctly. They are called _leaf traces_, and mark the points where +the fibrovascular bundles from the leaf veins passed into the stem. +Look on the bark, or epidermis, for lenticels. + +=147. Bud scales and scars.=—Notice the stout, hard scales by which +the winter buds are covered in most of our hardy trees and shrubs. +Remove these from the terminal one of your specimen, and notice the +ring of scars left around the base. Look lower down on your twig +for a ring of similar scars left from last year’s bud. Is there any +difference in the appearance of the bark above and below this ring? +If so, what is it, and how do you account for it? Is there more than +one of these rings of scars on your twig, and if so, how many? How +old is the twig and how much did it grow each year? Has its growth +been uniform, or did it grow more in some years than in others? + +[Illustration: FIG. 150.—Diagram of opposite bud scales.] + +=148. Arrangement and use of the scales.=—Notice the manner in +which the scales overlap so as to “break joints,” like shingles +on the roof of a house. Where the leaves are opposite, the manner +of superposition is very simple. Remove the scales one by one, +representing the number and position of the pairs by a diagram +after the model given in Fig. 150. In the bud of an alternately +branched twig the order will be different, and the diagram must be +varied accordingly. Do you observe any difference as to size and +texture between the outer and inner scales? Notice how the former +inclose the tenderer parts within like a protecting wall. In cold +climates the outer scales are frequently coated with gum, as in the +horse-chestnut, for greater security against the weather. The hickory +and various other trees have the inner scales covered with fur or +down that envelops the tender bud like a warm blanket. + +=149. Nature of the scales.=—The position of the scales shows +that they occupy the place of leaves or of some part of a leaf. +In expanding buds of the lilac and many other plants, they can be +found in all stages of transition, from scales to true leaves. In +the buckeye and horse-chestnut, they will easily be recognized as +modified leaf stalks (Fig. 151). In the tulip tree, magnolia, India +rubber tree, fig, elm, and many others, they represent appendages +called _stipules_, often found at the bases of leaves. (See 165, +166.) In this case a pair of scales is attached with each separate +leaflet, and as the growing axis lengthens in spring, they are +carried apart by the elongation of the internodes so that the scars +are separated, a pair at each node, making rings all along the stem, +as shown in Fig. 152, instead of having them compacted into bands at +the base of the bud. These scars are sometimes very persistent, and +in the common fig and magnolia may often be traced on stems six to +eight years old. Do they furnish any indication as to the relative +age of the different parts of the stem, like the bands of scars on +twigs of horse-chestnut and hickory? Give a reason for your answer. +(Fig. 152.) + +[Illustration: FIG. 151.—Development of the parts of the bud in the +buckeye. (_After_ GRAY.)] + +[Illustration: FIG. 152.—Stem of tulip tree: _s_, _s_, scars left by +stipular scales; _l_, _l_, leaf scars.] + +=150. Different rates of growth.=—Notice the very great difference +between branches in this respect. Sometimes the main stem will have +lengthened from twenty to fifty centimeters or more in a single +season, while some of the lateral ones will have grown but an inch +or two in four or five seasons. One reason for this is because the +terminal bud, being on the great trunk line of sap movement, gets +a larger share of nourishment than the others, and being stronger +and better developed to begin with, starts out in life with better +chances of success. + +Make a drawing of your specimen, showing all the points brought out +in the examination just made. Cut sections above and below a set of +bud scars and count the rings of annual growth in each section. What +is the age of each? How does this agree with your calculation from +the number of scar clusters left by the bud scales? + +=151. Irregularities.=—Take a larger bough of the same kind that you +have been studying, and observe whether the arrangement of branches +on it corresponds with the arrangement of buds on the twig. Did +all the buds develop into branches? Do those that did develop all +correspond in size and vigor? If all the buds developed, how many +branches would a tree produce every year? + +In the elm, linden, beech, hornbeam, hazelnut, willow, and various +other plants, the terminal bud always dies and the one next in order +takes its place, giving rise to the more or less zigzag axis that +generally characterizes trees of these species. (Fig. 153.) + +[Illustration: FIG. 153.—Bud development of beech: _a_, as it is, +many buds failing to develop; _b_, as it would be if all the buds +were to live.] + +=152. Forked stems.=—Take a twig of buckeye, horse-chestnut, or +lilac, and make a careful sketch of it, showing all the points that +were brought out in the examination of your previous specimen. Which +is the larger, the lateral or the terminal bud? Is their arrangement +alternate or opposite? What was the leaf arrangement? Count the leaf +traces in the scars; are they the same in all? If all the buds had +developed into branches, how many would spring from a node? Look for +the rings of scars left by the last season’s bud scales. Do you find +any twig of more than one year’s growth, as measured by the scar +rings? + +[Illustration: FIG. 154.—Two-forked twig of horse-chestnut.] + +Look down between the forks of a branched stem for a round scar. +This is not a leaf scar, as we can see by its shape, but one left by +the last season’s flower cluster. The flower, as we know, dies after +perfecting its fruit, and so a flower bud cannot continue the growth +of its axis as other buds do, but has just the opposite effect and +stops all further growth in that direction. Hence, stems and branches +that end in a flower bud cannot continue to develop their main axis, +but their growth is usually carried on, in alternate-leaved stems, by +the nearest lateral bud, or in opposite-leaved ones, by the nearest +pair of buds. In the first case there results the zigzag spray +characteristic of such trees as the beech and elm (Fig. 155, _B_); in +the second, the two-forked, or _dichotomous_ branching, exemplified +by the buckeye, horse-chestnut, jimson weed, mistletoe, and dogwood +(Fig. 155, _A_). + +Draw a diagram of the buckeye, or other dichotomous stem, as it would +be if all the buds developed into branches, and compare it with +your diagrams of excurrent and deliquescent growth. Draw diagrams +to illustrate the branching of the elm, beech, lilac, linden, rose, +maple, or their equivalents. + +[Illustration: FIG. 155.—Diagrams of two-forked branching. The +pointed bodies in the forks shows where terminal flower buds or +flower clusters have changed the direction of growth.] + +=153. Definite and indefinite annual growth.=—The presence or absence +of terminal buds gives rise to another important distinction in +plant development—that of _definite_ and _indefinite_ annual growth. +Compare with any of the twigs just examined, a branch of rose, honey +locust, sumac, mulberry, etc., and note the difference in their +modes of termination. The first kind, where the bough completes its +season’s increase in a definite time and then devotes its energies to +developing a strong terminal bud to begin the next year’s work with, +are said to make a _definite or determinate annual growth_. Those +plants, on the other hand, which make no provision for the future, +but continue to grow till the cold comes and literally nips them in +the bud, are _indefinite_, or _indeterminate_ annual growers. Notice +the effect of this habit upon their mode of branching. The buds +toward the end of each shoot, being the youngest and tenderest, are +most readily killed off by frost or other accident, and hence new +branches spring mostly from the older and stronger buds near the base +of the stem. It is their mode of branching that gives to plants of +this class their peculiar bushy aspect. Such shrubs generally make +good hedges on account of their thick undergrowth. The same effect +can be produced artificially by pruning. + +[Illustration: FIG. 156.—A mixed wood in winter, showing the trend of +the branches.] + +=154. Differences in the branching of trees.=—We are now prepared +to understand something about the causes of that endless variety in +the spread of bough and sweep of woody spray that makes the winter +woods so beautiful. Where the terminal bud is undisputed monarch +of the bough, as in the pine and fir, or where it is so strong and +vigorous as to overpower its weaker brethren and keep the lead, as +in the magnolia, tulip tree, and holly, we have excurrent growth. In +plants like the oak and apple, where all the buds have a more nearly +equal chance, the lateral branches show more vigor, and the result is +either deliquescent growth, or a mixture of the two kinds. In the elm +and beech, where the usurping pseudo-terminal bud keeps the mastery, +but does not completely overpower its fellows, we find the long, +sweeping, delicate spray characteristic of those species. Examine a +sprig of elm, and notice further that the flower buds are all down +near the base of the stem, while the leaf buds are near the tip. The +chief development of the season’s growth is thus thrown toward the +end of the branch, giving rise to that fine, feathery spray which +makes the elm an even more beautiful object in winter than in summer +(Fig. 158). + +An examination of the twigs of other trees will bring out the various +peculiarities that affect their mode of branching. The angle, for +instance, which a twig makes with its bough has a great effect in +shaping the contour of the tree. Compare in this respect the elm and +hackberry; the tulip tree and willow; ash and hickory. As a general +thing, acute angles produce slender, flowing effects; right or obtuse +angles, more bold and rugged outlines. + +[Illustration: FIG. 157.—Winter spray of ash, an opposite-leaved +tree.] + +[Illustration: FIG. 158.—Winter spray of elm.] + + + Practical Questions + + 1. Has the arrangement of leaves on a twig anything to do with the + way a tree is branched? (145, 151, 152.) + + 2. Why do most large trees tend to assume the excurrent, or axial, + mode of growth if let alone? (150, 154.) + + 3. If you wished to alter the mode of growth, or to produce what + nurserymen call a low-headed tree, how would you prune it? (152, + 153.) + + 4. Would you top a timber tree? (152, 153.) + + 5. Are low-headed or tall trees best for an orchard? Why? + + 6. Why is the growth of annuals generally indefinite? + + 7. Name some trees of your neighborhood that are conspicuous for + their graceful winter spray. + + 8. Name some that are characterized by sharpness and boldness of + outline. + + 9. Account for the peculiarities in each case. + + + II. BUDS + + MATERIAL.—Expanding leaf and flower buds in different stages of + development; large ones show the parts best and should be used + where attainable. Some good examples for the opposite arrangement + are horse-chestnut, maple, lilac, ash; for the alternate: hickory, + sweet gum, balsam poplar, beech, elm. Where material is scarce, the + twigs used in the last section may be placed in water and kept till + the buds begin to expand. + +=155. Folding of the leaves.=—Remove the scales from a bud of +horse-chestnut nearly ready to open, and notice the manner in +which the young leaves are folded. This is called _vernation_, or +_prefoliation_, words meaning respectively “spring condition” and +“condition preceding the leaf.” Leaves are packed in the bud so as to +occupy the least space possible, and in different plants they will be +found folded in a great many different ways, according to the shape +and texture of the leaf and the space available for it in the bud. +When doubled back and forth like a fan, or crumpled and folded as in +the buckeye, horse-chestnut, and maple, the vernation is _plicate_ +(Figs. 160, 162). + +[Illustration: FIG. 159.—Expanding bud of English walnut, showing +twice conduplicate vernation.] + +[Illustration: FIG. 160.—A partly expanded leaf of beech, showing +plicate-conduplicate vernation.] + +=156. Position of the flower cluster.=—What do you find within the +circle of leaves? Examine one of the smaller axillary buds, and +see if you find the same object within it. If you are in any doubt +as to what this object is, examine a bud that is more expanded, +and you will have no difficulty in recognizing it as a rudimentary +flower cluster. Notice its position with reference to the scales and +leaves. If at the center of the bud, it will, of course, terminate +its axis when the bud expands, and the growth of the branch will +culminate in the flower. The branching of any kind of stem that +bears a central flower cluster must, then, be of what order? Compare +your drawings with the section of a hyacinth bulb or jonquil, and +note the similarity in position of the flower clusters. In a bud +of the hickory, walnut, oak, etc., the position of the flower +clusters is different from that of flowers in the buds of lilac +and horse-chestnut. Look for a bud containing them, and find out +where they occur. Can the axis continue to grow after flowering, +in this kind of stem? Give a reason for your answer. Make sketches +in transverse and longitudinal section (see Figs. 162, 163) of two +different kinds of buds, illustrating the terminal and axillary +position of the flower cluster. + +[Illustration: FIGS. 161, 162.—Buds of maple: 161, vertical section +of a twig; 162, cross section through bud, showing folded leaves in +center and scales surrounding them.] + +[Illustration: FIG. 163.—Vertical section of hickory bud: _a_, furry +inner scales; _b_, outer scales; _l_, folded leaf; _r_, receptacle.] + +=157. Dormant buds.=—A bud may often lie dormant for months or even +years, and then, through the injury or destruction of its stronger +rivals, or some other favoring cause, develop into a branch. Such +buds are said to be _latent_ or _dormant_. The sprouts that often put +up from the stumps of felled trees originate from this source. + +[Illustration: FIG. 164.—Twig of red maple, showing supernumerary +bud, _b_; _rs_, ring of scars left by last year’s bud scales. +(_After_ GRAY.)] + +=158. Supernumerary buds.=—Where more than one bud develops at a +node, as is so often the case in the oak, maple, honey locust, +etc., all except the normal one in the axil are _supernumerary_ +or _accessory_. These must not be confounded with _adventitious_ +buds—those that occur elsewhere than at a node. + + + Practical Questions + + 1. Would protected buds be of any use to annuals? Why, or why not? + + 2. Of what use is the gummy coating found on the buds of the + horse-chestnut and balm of Gilead? (148.) + + 3. Can you name any plants the buds of which serve as food for man? + + 4. How do flower buds differ in shape from leaf buds? + + 5. At what season can the leaf bud and the flower bud first be + distinguished? Is it the same for all flowering plants? + + 6. Watch the different trees about your home, and see when the buds + that are to develop into leaves and flowers the next season are + formed in each species. + + + III. THE BRANCHING OF FLOWER STEMS + + MATERIAL.—Typical flower clusters illustrating the definite and + indefinite modes of inflorescence. Some of those mentioned in the + text are:— + + Indefinite: hyacinth, shepherd’s purse, wallflower, carrot, lilac, + blue grass, smartweed (_Polygonum_), wheat, oak, willow, clover. + + Definite: chickweed, spurge (_Euphorbia_), comfrey, dead nettle, + etc. Any examples illustrating the principal kinds of cluster will + answer. + +=159. Inflorescence= is a term used to denote the position and +arrangement of flowers on the stem. It is merely a mode of branching, +and follows the same laws that govern the branching of ordinary stems. + +The stalk that bears a flower is called the _peduncle_. In a cluster +the main axis is the common peduncle, and the separate flower stalks +are _pedicels_. A simple leafless flower stalk that rises directly +from the ground, like those of the dandelion and daffodil, is called +a _scape_ (Fig. 165). + +[Illustration: FIG. 165.—Solitary terminal flower of a lily.] + +[Illustration: FIG. 166.—Indeterminate inflorescence of moneywort. +(_After_ GRAY.)] + +=160. Two kinds of inflorescence.=—The growth of flower stems, +like that of leaf stems, is of two principal kinds, definite and +indefinite, or, as it is frequently expressed, determinate and +indeterminate. The simplest kind of each is the solitary, a single +flower either terminating the main axis, as the tulip, daffodil, +trillium, magnolia, etc., or springing singly from the axils, as the +running periwinkle, moneywort, and cotton. + +[Illustration: FIG. 167.—Raceme of milk vetch (_Astragalus_).] + +[Illustration: FIG, 168.—Catkins of aspen.] + +=161. Indeterminate inflorescence= is always axillary, since the +production of a terminal flower would stop further growth in that +direction and thus terminate the development of the axis. The +_raceme_ is the typical flower cluster of the indefinite sort. In +such an arrangement the oldest flowers are at the lower nodes, +new ones appearing only as the axis lengthens and produces new +internodes. The little scale or _bract_ usually found at the base of +the pedicel in flower clusters of this sort is a reduced leaf, and +the fact that the flower stalk springs from the axil shows it to be +of the essential nature of a branch. When the flowers are sessile +and crowded on the axis in various degrees, the cluster produced may +be a _spike_, as seen in the plantain, knotweed, etc., or a _head_, +like that of the clover, buttonwood, and sycamore. The _catkins_ that +form the characteristic inflorescence of most of our forest trees +are merely pendant spikes. The _corymb_ is a modification of the +raceme in which the lower pedicels are elongated so as to place their +flowers on a level with those of the upper nodes, making a convex, or +more or less flat-topped cluster, as in the wallflower and hawthorn. +The _umbel_ differs from the corymb in having the pedicels with their +bracts all gathered at the top of the peduncle, from which they +spread in every direction like the rays of an umbrella, as the name +implies. This is the prevalent type of flower cluster in the parsley +family, which takes its botanical name, _Umbelliferæ_, from its +characteristic form of inflorescence. The pedicels of an umbel are +called _rays_, and the circle of bracts at the base of the cluster is +an _involucre_. + +[Illustration: FIG. 169.—Corymb of plum blossoms.] + +[Illustration: FIG. 170.—Umbel of milkweed.] + +[Illustration: FIG. 171.—Panicle of grass, a compound cluster of the +racemose type.] + +[Illustration: FIG. 172.—Flat-topped cyme of sneezeweed.] + +=162. Determinate, or cymose, inflorescence.=—In the _cyme_, the +typical cluster of the determinate kind, the older blossoms in the +center, being terminal, stop the axis of growth in that direction and +force the stem, in continuing its growth, to send out side branches +from the axils of the topmost leaves, in a manner precisely similar +to the two-forked branching of stems like the horse-chestnut and +jimson weed. When the older peduncles are lengthened as described +in 161, a flat-topped cyme is produced, which is distinguished +from the corymb by its order of flowering, the oldest blossoms +being at the center, while in the corymb they appear in the reverse +order. A peculiar form of cyme is found in the scorpioid or coiled +inflorescence of the pink-root (_Spigelia_), heliotrope, comfrey, +etc. Its structure will be made clear by an inspection of Figs. +174-176. + +[Illustration: FIG. 173.—Scorpioid cyme.] + +=163. The nature of flower stems.=—A comparison of the types of +inflorescence with the modes of branching in ordinary stems (144, +152, 153) will show a strict correspondence between them. Both bear +leaves and buds, and the individual flowers of a cluster usually +spring from the axils of leaves or from bracts, which are merely +reduced leaves. What, then, is the essential nature of flower stems? + +[Illustration: FIGS. 174-176.—Diagrams of cymose inflorescence, with +flowers numbered in the order of their development: 174, cyme half +developed (scorpioid); 175, a flat-topped or corymbose cyme; 176, +development of a typical cyme.] + +=164. Significance of the clustered arrangement.=—As a general thing +the clustered arrangement marks a higher stage of development than +the solitary, just as in human life the rudest social state is a +distinct advance upon the isolated condition of the savage. In plant +life it is the beginning of a system of coöperation and division of +labor among the associated members of the flower cluster, as will be +seen later when we take up the study of the flower. + + + Practical Questions + + 1. Name as many solitary flowers as you can think of. + + 2. Do you, as a rule, find very small flowers solitary, or in + clusters? + + 3. Would the separate flowers of the clover, parsley, or grape be + readily distinguished by the eye among a mass of foliage? + + 4. Should you judge from these facts that it is, in general, + advantageous to plants for their flowers to be conspicuous? + + + Field Work + + (1) In connection with 144-154, the characteristic modes of + branching among the common trees and shrubs of each neighborhood + should be observed and accounted for. The naked branches of the + winter woods afford exceptional opportunities for studies of this + kind, which cannot well be carried on except out of doors. Note + the effect of the mode of branching upon the general outline of + the tree; compare the direction and mode of growth of the larger + boughs with that of small twigs in the same species, and see if + there is any general correspondence between them; note the absence + of fine spray on the boughs of large-leaved trees, and account + for it. Account for the flat sprays of trees like the elm, beech, + hackberry, etc.; the irregular stumpy branches of the oak and + walnut; the stiff straight twigs of the ash; the zigzag switches of + the black locust, Osage orange, elm, and linden. Measure the twigs + on various species, and see if there is any relation between the + length and thickness of branches. Notice the different trend of + the upper, middle, and lower boughs in most trees, and account for + it. Observe the mode of branching of as many different species as + possible of some of the great botanical groups of trees; the oaks, + hickories, hawthorns, and pines, for instance, and notice whether + it is, as a general thing, uniform among the species of the same + group, and how it differs from that of other groups. + + (2) In connection with 155-158, buds of as many different kinds + as possible should be examined with reference to their means of + protection, their vernation and leaf arrangement, and the resulting + modes of growth. Compare the folding of the cotyledons in the seed + with the vernation of the same plants, and observe whether the + folding is the same throughout a whole group of related plants, + or only for the same species. Notice which modes seem to be most + prevalent. Select a twig on some tree near your home or your + schoolhouse, and keep a record of its daily growth from the first + sign of the unfolding of its principal bud to the full development + of its leaves. Any study of buds should include an observation of + them in all stages of development. + + (3) With 160-165, study the inflorescence of the common plants and + weeds that happen to be in season, until you have no difficulty + in distinguishing between the definite and indefinite sorts, and + can refer any ordinary cluster to its proper form. Notice whether + there is any tendency to uniformity in the mode of inflorescence + among flowers of the same family. Consider how each kind is adapted + to the shape and habit of the flowers composing it, and what + particular advantage each of the specimens examined derives from + the way its flowers are clustered. In cases of mixed inflorescence, + see if you can discover any reason for the change from one form to + the other. + + + + +CHAPTER VI. THE LEAF + + + I. THE TYPICAL LEAF AND ITS PARTS + + MATERIAL.—Leaves of different kinds showing the various modes of + attachment, shapes, texture, etc. For stipules, leaves on very + young twigs should be selected, as these bodies often fall away + soon after the leaves expand. The rose, Japan quince, willow, + strawberry, pea, pansy, and young leaves of beech, apple, elm, + tulip tree, India rubber tree, magnolia, knotweed, furnish good + examples of stipules. For the different orders of leaf arrangement, + lilac, maple, spurge, trillium, cleavers (Galium) show the opposite + and whorled kinds. Elm, basswood, grasses; alder, birch, sedges; + peach, apple, cherry, show respectively for each group the three + principal orders of alternate arrangement. + +=165. Parts of the leaf.=—Examine a young, healthy leaf of apple, +quince, or elm, as it stands upon the stem, and notice that it +consists of three parts: a broad expansion called the _blade_; a +leaf stalk or _petiole_ that attaches it to the stem; and two little +leaflike or bristle-like bodies at the base, known as _stipules_. +Make a sketch of any leaf provided with all these parts, and label +them, respectively, blade, petiole, and stipules. These three parts +make up a perfect or typical leaf, but as a matter of fact, one or +more of them is usually wanting. + +[Illustration: FIG. 177.—A typical leaf and its parts: _b_, blade; +_p_, petiole; _s_, _s_, stipules.] + +[Illustration: FIG. 178.—Spiny stipules of clotbur.] + +=166. Stipules.=—The office of stipules, when present, is generally +to subserve in some way the purposes of protection. In many cases, +as in the fig, elm, beech, oak, magnolia, etc., they appear only as +protective scales that cover the bud during winter, and fall away as +soon as the leaf expands. When _persistent_, that is, enduring, they +take various forms according to the purposes they serve. But under +whatever guise they occur, their true nature may be recognized by +their position on each side of the base of the petiole, and not in +the _axil_, or angle formed by the leaf with the stem. (149.) + +[Illustration: FIG. 179.—Adnate stipules of clover. FIG. 180.—Leaves +of smilax, showing stipular tendrils. FIG. 181.—Leafy stipules of +Japan quince.] + +=167. Leaf attachment.=—The normal use of the petiole is to secure a +better light exposure for the leaves, but, like other parts, it is +subject to modifications, and is often wanting altogether. In this +case the leaf is said to be _sessile_, that is, _seated_, on the +stem, and the leaf bases are designated by various terms descriptive +of their mode of attachment. The meaning of these terms, when not +self-explanatory, can best be learned by a comparison of living +specimens with Figs. 184-187. + +=168. Arrangement of leaves on the stem.=—The mode of attachment is +something quite distinct from the mode of leaf arrangement on the +stem, or _phyllotaxy_, as it is termed by botanists. It was seen in +148 that this takes place in two different ways, the alternate and +opposite. These two kinds of arrangement represent the principal +forms of leaf disposition on the stem, the different varieties of +each depending on the manner in which the leaves are distributed. + +[Illustration: FIGS. 182-187.—Petioles, and leaf attachment: 182, +petioles of jasmine nightshade (_Solanum jasminoides_) acting as +tendrils; 183, acacia, showing petiole transformed to leaf blade; +184, sessile leaves of epilobium; 185, clasping leaf of lactuca; 186, +perfoliate leaves of uvularia; 187, peltate leaf of tropæolum. (182 +and 186 _after_ GRAY.)] + +Where three or more occur at a node, as in the trillium and cleavers +(_Galium_), they constitute a whorl, which is only a variant of the +opposite arrangement. There is no limit to the number of leaves that +may be in a whorl except the space around the stem to accommodate +them. + +The phyllotaxy of alternate leaves is more complicated. The +different forms are characterized by the angular distance between the +points of leaf insertion around the stem. In the elm, basswood, and +most grasses, they are distributed in two rows or ranks on opposite +sides of the stem, each just half way round the circumference from +the one next in succession (Fig. 189), the third in vertical order +standing directly over the first. In most of our common trees and +shrubs five leaves are passed in making two turns round the stem, the +sixth leaf in vertical order standing over the first. This is called +the five-ranked arrangement, and is the most common order among +dicotyls. + +[Illustration: FIG. 188.—Whorled leaves of Indian cucumber.] + +[Illustration: FIG. 189.—Twig of a hackberry (_Celtis cinerea_), +showing the two-ranked arrangement. Notice how the position of the +stems and branches of the main axis corresponds to that of the +leaves.] + +=169. Relation between the shape and arrangement of +leaves.=—Phyllotaxy is of importance chiefly on account of its +influence on the light relation of leaves. A compact, close-ranked +arrangement tends to shut off the light from the lower nodes, and +hence, in plants where it prevails, the leaves are apt to be long +and narrow in proportion to the frequency of the vertical rows. +The yucca, oleander, Canada fleabane and bitterweed (_Helenium +tenuifolium_), illustrate this relation. + +[Illustration: PLATE 9.—Vegetation of a moist, shady ravine. Notice +the expanded surface of the leaf blades and the long internodes that +separate the individual leaves. (From Rep’t. Mo. Botanical Garden.)] + +[Illustration: FIG. 190.—Narrow leaves in crowded vertical rows.] + +On the other hand, when the leaves are large and rounded in outline, +as those of the sunflower, hollyhock, and catalpa, they are usually +separated by longer internodes, or their blades are cut and incised +so that the sunlight easily strikes through to the lower ones. + +=170. Other external characteristics= to be observed in leaves are:— + +(1) General Outline: whether round, oval, heart-shaped, etc. (Figs. +191-197). + +(2) Margins: whether unbroken (_entire_), or variously toothed and +indented. (Figs. 198-202.) + +(3) Texture: whether thick, thin, soft, hard, fleshy, leathery, +brittle. + +(4) Surface: smooth, shining, dull, wrinkled, hairy, or otherwise +roughened. + +[Illustration: FIGS. 191-197.—Shapes of leaves: 191, lanceolate; 192, +spatulate; 193, oval; 194, obovate; 195, kidney-shaped; 196, deltoid; +197, lyrate. (191-195 _after_ GRAY.)] + +Not only do leaves of different kinds exhibit these characteristics +in varying degrees, but young and old leaves, or those on young and +old plants of the same kind, often differ from each other in color, +size, shape, texture, mode of attachment, and the like, to such a +degree (Figs. 203, 204) that one not familiar with them in both +stages would hardly recognize them as belonging to the same species. +The young leaves of eucalyptus, mulberry, and some oaks afford +conspicuous examples of such differences, and they exist between the +cotyledons and mature leaves of most plants. + +Can you see any benefit, in the case of the plant whose leaves you +are studying, that could be derived from such of the characteristics +named above as they may exhibit? + +[Illustration: FIGS. 198-202.—Margins of leaves: 198, serrate; 199, +dentate; 200, crenate; 201, undulate; 202, sinuate. (_After_ GRAY.)] + +[Illustration: FIGS. 203, 204.—Leaves of paper mulberry tree: 203, +leaf from an old tree; 204, leaf from a two-year-old sprout.] + + + Practical Questions + + 1. Tell the nature and use of the stipules in such of the following + plants as you can find: tulip tree; fig; beech; apple; willow; + pansy; garden pea; Japan quince (_Pyrus Japonica_); sycamore; rose; + paper mulberry (_Broussonetia_). + + 2. How would you distinguish between a chinquapin, a chestnut, a + chestnut oak, and a horse-chestnut tree by their leaves alone? By + their bark and branches? Between a hickory, ash, common elder, box + elder, ailanthus, sumach? Between beech, birch, elm, hackberry, + alder? + + (Any other sets of leaves may be substituted for those named, the + object being merely to form the habit of distinguishing readily the + differences and resemblances among those that bear some general + likeness to one another.) + + 3. From the study of these or similar specimens, would you conclude + that resemblances in leaves are confined to those of closely + related kinds? + + 4. Name some causes independent of botanical relationship that + might influence them. (169, 170; Exps. 48, 57.) + + 5. Do you find, as a general thing, more leaves with stipules or + without? + + 6. Is their absence from a mature leaf always a sign that it is + really exstipulate? (166.) + + 7. Can you trace any line of development through intervening + forms from a merely sessile leaf, like that of the pimpernel or + specularia, to a peltate one? (Figs. 184-187, and observation of + living specimens.) + + 8. Does the leaf determine the position of the node, or the node + the position of the leaf? + + 9. Strip the leaves from a twig of one order of arrangement and + replace them with foliage from a twig of a different order; for + instance, place basswood upon white oak, birch upon lilac, elm upon + pear, honeysuckle upon barberry, etc. Is the same amount of surface + exposed as in the natural order? + + 10. What disadvantage would it be to a plant if the leaves were + arranged so that they stood directly over one another? (169.) + + 11. Why are the internodes of vigorous young shoots, or scions, + generally so long? (150.) + + 12. If the upward growth of a stem or branch is stopped by pruning, + what effect is produced upon the parts below, and why? (152, 153.) + + 13. Give some of the reasons why corn grows so small and stunted + when sown broadcast for forage? (60, 63, 169.) + + 14. What is the use of “chopping” (_i.e._ thinning out) cotton? + + + II. THE VEINING AND LOBING OF LEAVES + + MATERIAL.—Leaves of any monocotyl and dicotyl will show the + difference between parallel and net-veining. To illustrate the + palmate and pinnate kinds, the leaves of grasses and arums may be + used for monocotyls, and for dicotyls, those of ivy, maple, grape, + elm, peach, cherry, etc.; for division, examine lobed and compound + leaves of as many kinds as are attainable. A specimen showing each + kind of veining should be placed in coloring fluid a short time + before the lesson begins. The leafstalks of celery and plantain + are excellent for showing the relation between the leaf veins and + vascular system of the plant. + +=171. Parallel and net veining.=—Compare a leaf of the wandering +Jew, lily, or any kind of grass, with one of grape, ivy, or willow. +Hold each up to the light, and note the veins or little threads of +woody substance that run through it. Make a drawing of each so as to +show plainly the direction and manner of veining. Write under the +first, _parallel-veined_, and under the second, _net-veined_. This +distinction of leaves into parallel and net-veined corresponds with +the two great classes into which seed-bearing plants are divided, +monocotyls, as a general thing, being characterized by the first +kind, and dicotyls by the second. + +[Illustration: FIG. 205.—Parallel-veined leaf of lily of the valley +(_After_ GRAY).] + +[Illustration: FIG. 206.—Net-veined leaf of a willow.] + +[Illustration: FIG. 207.—Pinnately parallel-veined leaf of calla lily +(_After_ GRAY).] + +[Illustration: FIG. 208.—Palmately net-veined leaf of wild ginger.] + +=172. Pinnate and palmate veining.=—Next, compare a leaf of the +canna, calla lily, or any kind of arum, with one of the elm, peach, +cherry, etc. What resemblances do you notice between the two? What +differences? Which is parallel-veined and which is net-veined? Make +a drawing of each, and compare with the first two. Notice that in +leaves of this kind, the petiole is continued in a large central +vein, called the _midrib_, from which the secondary veins branch off +on either side like the pinnæ of a feather; whence such leaves are +said to be _pinnately_, or _feather_ veined, as in Figs. 206, 207. In +the cotton, maple, ivy, etc., on the other hand, the petiole breaks +up at the base of the leaf (Fig. 208) into a number of primary +veins or ribs, which radiate in all directions like the fingers from +the palm of the hand; hence, such a leaf is said to be _palmately_ +veined. Net-veined leaves—the plantain (Fig. 209), wild smilax, +beech, dogwood—are sometimes ribbed in a way that might lead an +inexperienced observer to confound them with parallel-veined ones, +but the reticulations between the ribs show that they belong to the +net-veined class. + +[Illustration: FIG. 209.—Ribbed leaf of plantain.] + +=173. Veins as a mechanical support.=—Hold up a stiff, firm leaf +of any kind, like the magnolia, holly, or India rubber, to the +light, having first scraped away a little of the under surface, and +examine it with a lens. Compare it with one of softer texture, like +the peach, maple, or clover. In which are the veins the closer and +stronger? Which is the more easily torn and wilted? Tear a blade of +grass longitudinally and then cross-wise; in which direction does it +give way the more readily? Tear apart gently a leaf of maple, or ivy, +and one of elm or other pinnately veined plant; in which direction +does each give way with least resistance? What would you judge from +these facts as to the mechanical use of the veins? + +=174. Effect upon shape.=—By comparing a number of leaves of each +kind it will be seen that the feather-veined ones tend to assume +elongated outlines (Figs. 197, 207); the palmate-veined ones, broad +and rounded forms (Figs. 195, 208). Notice also that the straight, +unbroken venation of parallel-veined leaves is generally accompanied +by smooth, unbroken margins, while the irregular, open meshes of +net-veined leaves are favorable to breaks and indentations. + +=175. Veins as water carriers.=—Examine a leaf from a stem that has +stood in red ink for an hour or two. Do you see evidence that it has +absorbed any of the liquid? Cut across the blade and examine with a +lens. What course has the absorbed liquid followed? What use does +this indicate for the veins, besides the one already noted? Observe +the point of insertion on the stem, and examine the scar with a lens: +do you see any evidence of a connection between the leaf veins and +the fibrovascular bundles of the stem? (111, 125, 126.) Notice where +and how the veins end. Are they of the same size all the way, or do +they grow smaller toward the tip? Are they separate and distinct, or +are they connected throughout their ramifications, like the veins and +arteries of the human body? How do you know? Do you see any of the +coloring fluid in the small reticulations between the veins? How did +it get there? + +=176. The nature and office of veins.=—We learn from 173 and 175 that +the veining serves two important purposes in the economy of the leaf: +first, as a skeleton or framework, to support the expanded blade; +and second, as a system of water pipes, for conveying the sap out +of which its food is manufactured. In other words the veins are a +continuation of the fibrovascular bundles into the leaves, by means +of which the latter are put in communication with the body of the +plant. + +=177. The relation between veining and lobing.=—Compare the outline +of a leaf of maple or ivy with one of oak or chrysanthemum. Do +you perceive any correspondence between the manner of lobing or +indentation of their margins, and the direction of the veins? (Figs. +210, 211.) To what class would you refer each one? + +The lobes themselves may be variously cut, as in the fennel and rose +geranium, thus giving rise to twice-cleft, thrice-cleft (Fig. 212), +four-cleft, or even still more intricately divided blades. + +=178. Compound leaves.=—Compare with the specimens just examined +a leaf of horse-chestnut, clover, or Virginia creeper, and one +of rose, black locust, or vetch. Notice that each of these last is +made up of entirely separate divisions or leaflets, thus forming a +_compound leaf_. Notice also that the two kinds of compound leaves +correspond to the two kinds of veining and lobing, so that we +have palmately and pinnately compound ones. In pinnate leaves the +continuation of the common petiole along which the leaflets are +ranged is called the _rhachis_. + +[Illustration: FIG. 210.—Pinnately lobed leaf of horse nettle. FIG. +211.—Palmately lobed leaf of grape.] + +[Illustration: FIG. 212.—Palmately parted leaf of a buttercup. FIG. +213.—Pinnately compound leaf of black locust.] + +[Illustration: FIG. 214.—Palmately compound leaf of horse-chestnut. +FIG. 215.—Pinnately trifoliolate leaf of a desmodium. FIG. +216.—Palmately trifoliolate leaf of wood sorrel.] + + + Practical Questions + + 1. In selecting leaves for decorations that are to remain several + hours without water, which of the following would you prefer, and + why: smilax or Madeira vine (_Boussingaultia_); ivy or Virginia + creeper; magnolia or maple; maidenhair or shield fern (_Aspidium_)? + (173.) + + 2. Would you select very young leaves, or more mature ones, and why? + + 3. Can you name any parallel-veined leaves that have their margins + lobed, or indented in any way? + + 4. Which are the more common, parallel-veined or net-veined leaves? + + 5. Why do the leaves of corn and other grains not shrivel + lengthwise in withering, but roll inward from side to side? (173.) + + 6. Can you name any palmately veined leaves in which the secondary + veins are pinnate? Any pinnately veined ones in which the secondary + veins are palmate? + + 7. Lay one of each kind before you; try to draw a pinnate leaf with + palmate divisions. Do you see any reason now why these so seldom + occur in nature? + + 8. Name some advantages to a plant in having its leaves cut-lobed + or compound. (169.) + + 9. Mention some circumstances under which it might be advantageous + for a plant to have large, entire leaves. (169; Plate 9.) + + 10. How would the floating qualities of the leaves of the pond lily + be affected if their blades were cut-lobed or compound? + + 11. Do the leaves of the red cedar and arbor vitæ contribute to + their value as shade trees? + + 12. Name some of the favorite shade trees of your neighborhood; do + they, as a general thing, have their leaves entire, or lobed and + compound? + + 13. Which of the following are the best shade trees, and why: pine, + white oak, mimosa (_Albizzia_), sycamore, locust, horse-chestnut, + fir, maple, linden, China tree, cedar, ash? + + 14. Which would shade your porch best, and why: cypress vine, + grape, gourd, morning-glory, wistaria, clematis, smilax, kidney + bean, Madeira vine, rose, yellow jasmine, passion flower? + + + III. TRANSPIRATION + + MATERIAL.—Leafy twigs of actively growing young plants. Sunflower, + corn, peach, grape, calla, and arums in general transpire rapidly; + thick-leaved evergreens and hairy or rough species, like mullein + and horehound more slowly. For Exp. 63, small-leaved, large-leaved, + and thick-leaved kinds will be needed. + + APPLIANCES.—Glass jars and bottles with air-tight stoppers; a + little vaseline, oil, gardener’s wax, thread, cardboard, and a pair + of scales. + + EXPERIMENT 62. TO SHOW WHY LEAVES WITHER.—Dry two self-sealing jars + thoroughly, by holding them over a stove or a lighted lamp for a + short time to prevent “sweating.” Place in one a freshly cut leafy + sprig of any kind, leaving the other empty. Seal both jars and set + them in the shade. Place beside them, but without covering of any + kind, a twig similar to the one in the jar. Both twigs should have + been cut at the same time, and their cut ends covered with wax or + vaseline, to prevent access of air. Look at intervals to see if + there is any moisture deposited on the inside of either jar. If + there is none, set them both in a refrigerator or cover with a wet + cloth and allow to cool for half an hour, and then examine again. + In which jar is there a greater deposit of dew? How do you account + for it? Take the twig out of the jar and compare its leaves with + those of the one left outside; which have withered the more, and + why? + + EXPERIMENT 63. TO MEASURE THE RATE AT WHICH WATER IS GIVEN OFF BY + LEAVES OF DIFFERENT KINDS.—Fill three glass vessels of the same + size with water and cover with oil to prevent evaporation. Insert + into one the end of a healthy twig of peach or cherry; into the + second a twig of catalpa, grape, or any large-leaved plant, and + into the third, one of magnolia, holly, or other thick-leaved + evergreen, letting the stems of all reach well down into the water. + Care must be taken to select twigs of approximately the same size + and age, since the absorbent properties of very young stems are + more injured by cutting and exposure than those of older ones. All + specimens should be cut under water as directed in Exp. 58. Weigh + all three vessels, and at the end of twenty-four hours, weigh + again, taking note of the quantity of liquid that has disappeared + from each glass. This will represent approximately the amount + absorbed by the leaves from the twigs to replace that given off. + Which twig has lost most? Which least? Note the condition of the + leaves on the different twigs; have they all absorbed water about + as rapidly as they have lost it? How do you know this? Pluck the + leaves from each twig, one by one, lay them on a flat surface + that has been previously measured off, into square inches or + centimeters, and thus form a rough estimate of the area covered by + each specimen. Make the best estimate you can of the number of + leaves on each tree, and calculate the number of kilograms of water + it would give off at that rate in a day. + + EXPERIMENT 64. THROUGH WHAT PART OF THE LEAF DOES THE WATER GET + OUT?—Take some healthy leaves of tulip tree, grape, tropæolum, + or any large, soft kind attainable. Cover with vaseline the + _leafstalk_ and _upper_ surface of one; the stalk and _under_ + surface of a second; the stalk and _both_ surfaces of a third, and + leave a fourth one untreated. Suspend all four in a dry place by + means of a thread attached to the petioles so that both surfaces + may be equally exposed. The leaves must be all of the same species, + and as nearly as possible of the same age, size, and vigor, and + care must be taken that none of the vaseline is rubbed off in + handling. Examine at intervals of a few hours. Which of the leaves + withers soonest? Which keeps fresh longest? From what part would + you conclude, judging by this experiment, that the water escapes + most rapidly? + +=179. Transpiration, nutrition, and growth.=—We learn from the +foregoing, and from Exps. 58 and 59, that plants give off moisture +very much as animals do by perspiration. The two processes must not +be classed together, however, for they are physiologically different. +The action, in plants, is called _transpiration_. It is usually +assumed that a large amount of water must pass through the plant +in order to bring to it the necessary supply of food material; but +since the entrance of mineral salts is brought about by osmosis, +conditioned by the living cells of the root; and since osmosis +of salts may take place in a direction opposite to that of the +greater movement of water, it follows that the entrance of salts is +independent of transpiration. + +Inasmuch, however, as a certain amount of water is necessary to bring +the living cells into a condition of turgor (7) so that they may +grow, it follows that there is a relation between transpiration and +growth. If transpiration exceeds absorption for any length of time, +the tissues will be depleted of their moisture, as is shown by the +wilting of crops in dry, hot weather; and if the unequal movement +continues long enough, the plant will die. Hence, a knowledge of the +laws governing this important function is necessary to all who are +interested in cultivating agricultural products. + +[Illustration: FIG. 217.—A “weeping tree,” showing the effect where +absorption exceeds transpiration. Notice the position of the tree +near the water where the roots have unlimited moisture. (_After_ +FRANCÉ.)] + +=180. Magnitude of the work of transpiration.=—Few people have any +idea of the enormous quantities of water given off by leaves. It +has been calculated that a healthy oak may have as many as 700,000 +leaves, and that 111,225 kilograms of water—equal to about 244,700 +pounds—may pass from its surface in the five active months from June +to October. At this rate 226 times its own weight may pass through it +in a year, and it would transpire water enough during that time to +cover the ground shaded by it to a depth of 20 feet![2] Lawn grass +gives off water at such a rate that a vacant lot of 150 × 50 feet, +if well turfed, would be capable of transpiring over a ton of water +a day. Compare these figures with the average yearly rainfall in our +Gulf States—53 inches, approximately—and you can form some estimate +of the injury done to a growing crop from this cause alone. The +moisture is drawn from the surface by shallow rooted weeds (81) and +dissipated through the leaves. In the case of forest trees the effect +is different. Their roots, striking deep into the soil, draw up water +from the lower strata and distribute it to the thirsty air in summer. + +As the water given off by transpiration is in the form of vapor, +it must draw from the plant the amount of heat necessary for its +vaporization, and thus has the effect of making the leaves and the +air in contact with them cooler than the surrounding medium. At the +same time the coolness and moisture of the air tend to check the +loss by evaporation from the surface soil. It is partly to this +cause, and not alone to their shade, that the coolness of forests is +due. Measurements at various weather bureau stations in the United +States show that in summer the temperature of oak woods is 4° C. +lower during the day than in the open, and as much higher at night. +In a beech wood in Germany the difference between the forest and the +general temperature amounted to as much as 7° C. + + + Practical Questions + + 1. Is there any foundation in fact for the accounts of “weeping + trees” and “rain trees” that we sometimes read about in the papers? + (180; Exp. 48.) + + 2. Can you explain the fact, sometimes noticed by farmers, that in + wooded districts, springs which have failed or run low during a dry + spell sometimes begin to flow again in autumn when the trees drop + their leaves, even though there has been no rain? (180; Exp. 63.) + + 3. Other things being equal, which would have the cooler, + pleasanter atmosphere in summer, a well-wooded region or a treeless + one? (180.) + + 4. Could you keep a bouquet fresh by giving it plenty of fresh air? + (Exp. 62.) + + 5. Why does a withered leaf become soft and flabby, and a dried one + hard and brittle? (7; Exp. 62.) + + 6. Why do large-leaved plants, as a general thing, wither more + quickly than those with small leaves? (Exp. 63.) + + 7. Is the amount of water absorbed always a correct indication of + the amount transpired? Explain. (179.) + + 8. Explain the difference between the withering caused by excessive + transpiration and the shrinkage of cells due to plasmolysis. Are + both of these physiological processes? + + 9. Why is it best to trim a tree close when it is transplanted? + (179, 180.) + + 10. Why should transplanting be done in winter or very early + spring, before the leaves appear? (180.) + + + IV. ANATOMY OF THE LEAF + + MATERIAL.—For study of the epidermis, leaves of the white garden + lily (_Lilium album_) are best, as the stomata can be seen on + their lower surface with the naked eye. Wandering Jew, Spanish + bayonet (_Yucca aloifolia_), anemone, narcissus, iris, canna, show + them under a hand lens, but less distinctly. For sections, beet, + mustard, and beech leaves may be used, or ready-mounted specimens + obtained of a dealer. + + A compound microscope is needed for a minute study of the leaf + structure. + +[Illustration: FIGS. 218, 219.—Stomata of white lily leaf: 218, +closed; 219, open. (_After_ GRAY.)] + +=181. Stomata.=—It was shown in Exp. 64 that the water of +transpiration escapes most rapidly, as a general thing, from the +under surface of leaves. To find out why this is so, a careful study +of the epidermis will be necessary. For this purpose procure, if +possible, the leaf of a white garden lily (_Lilium album_), wandering +Jew, Spanish bayonet (_Yucca aloifolia_), anemone, narcissus, iris, +or canna. The first-named is preferable, as the transpiration pores +can be seen on it with the naked eye. Examine the under surface +with a hand lens, and you will see that it is covered with small +eye-shaped dots like those shown in Figs. 218 and 219. Strip off +a portion of the epidermis, hold it up to the light on a piece of +moistened glass, and they can be seen quite clearly with a lens. +These dots are the pores through which the water vapor escapes in +transpiration, and through which air finds its way into the tissues +of the leaf. They are called _stomata_ (sing., _stoma_), from a Greek +word meaning “a mouth.” Look for stomata on the upper epidermis; do +you find any, and if so, are there as many as on the under surface? +Do you see any relation between this fact and the results obtained +from Exp. 64? Can you see any good reasons why the stomata should be +placed on the under side in preference to the upper? Are they as much +exposed to excessive light and heat, or as liable to be choked by +dust, rain, and dew here as on the upper side? + +=182. Distribution of stomata.=—While stomata are generally more +abundant on the under side of leaves, this is not always the case. +In vertical leaves, like those of the iris, which have both sides +equally exposed to the sun, they are distributed equally on both +sides. In plants like the water lily, where the under surface lies +upon the water, they occur only on the upper side. Succulent leaves, +as a general thing, have very few, because they need to conserve all +their moisture. Submerged leaves have none at all; why? + +[Illustration: FIG. 220.—A small piece of the under epidermis of +an oak leaf, highly magnified to show the stomata, _g_, and minute +hairs, _h_.] + +[Illustration: FIG. 221.—Under epidermis of an oat leaf, showing +stomata.] + +=183. Minute study of a leaf epidermis.=—Place a bit of the lower +epidermis of a leaf under the microscope, and examine with a high +power. It will appear, if a monocotyl, to be composed of long, flat, +rectangular spaces (Fig. 221); if the leaf of a dicotyl is used, +they will be more or less irregular (Fig. 220), with the outlines +fitting into each other like the tiling of a floor or the blocks of a +Chinese puzzle. These spaces are the cells of the epidermis, and the +lines are the cell walls. Can you find any of the cell contents? The +cell sap is not often visible; do you see the nuclei? Can you give +a reason why the epidermal cells are so thin and flat? Between some +of the cells you will see two kidney-shaped bodies placed with their +concave sides together so as to leave a lenticular opening between +them. This is a _stoma_, and the kidney-shaped bodies (Figs. 218, +219) are _guard cells_. They are given this name because they open +or close the mouth of the stoma. If you will imagine a toy balloon +made in the form of a hollow ring, like the tire of a bicycle, you +can easily see, from Figs. 218, 219, that when the ring is strongly +inflated, it will expand, and in enlarging its own circumference, +will at the same time increase the diameter of the opening in the +center. When the expansive force is removed, it collapses, thus +closing, or greatly reducing, the aperture. + +[Illustration: FIG. 222.—Outline of a stoma of hellebore in vertical +section. The darker lines show the shape assumed by the guard cells +when the stoma is open; the lighter lines, when the stoma is closed. +The cavities of the guard cells with the stoma closed are shaded, and +are distinctly smaller than when the stoma is open.] + +In the same way the guard cells, when there is abundance of water in +them, expand, thus opening the stoma so that the water vapor passes +out more readily. But when there is a dearth of moisture, or when, +by reason of chemical action in the soil, the roots fail to supply +it, the leaves wilt, the guard cells, losing their water, collapse, +closing the pore, and transpiration is thus prevented or greatly +retarded. (Fig. 222.) + +Sketch a portion of the epidermis as it appears under the microscope, +labeling the parts. If stomata can be found in both conditions, make +sketches showing them both open and closed. + +=184. Internal structure of a leaf.=—Roll a leaf blade, or fold it +tightly to facilitate cutting, and with a scalpel, or a very sharp +razor, cut the thinnest possible slice through the roll. This will +give a section at right angles to the epidermis. It should be so +thin as to appear almost transparent. Put a small bit of a section +in a drop of water on a slide, place under the microscope, using a +high power, and look for the parts shown in Fig. 223. Notice the +horizontally flattened cells of the upper epidermis, _e_, and of the +lower epidermis, _e′_; also the vertically elongated palisade cells, +_p_, filled with particles of green coloring matter. These particles +are the chlorophyll bodies, to which the green color of the leaf is +due. They are the active agents in the manufacture of plant food, +and in a leaf removed from the plant during the day time and viewed +under a high power, the chlorophyll bodies, on treatment with iodine, +will be seen to contain granules of starch which they are in the act +of elaborating. The collecting cells, _t_, receive the assimilated +product from the palisade cells and pass it on through the spongy +parenchyma, _sch_, to the fibrovascular bundles. Notice how much +more abundant the green matter is in the upper part of the leaf than +in the lower; has this anything to do with the deeper color of the +upper surfaces of leaves? Notice the opening, _st_, lower epidermis; +do you recognize it? (See Fig. 222.) It is a stoma, seen in vertical +section. Notice the intercellular air spaces, _i_, _i_, in the spongy +parenchyma, and the much larger one, _a_, just behind the stoma. Why +is this last so much larger? + +[Illustration: FIG. 223.—Transverse section through a leaf of beet: +_e_, upper epidermis; _e′_, lower epidermis; _st_, stoma; _a_, air +space; _p_, palisade cells; _t_, collecting cells; _sch_, spongy +parenchyma; _i_, _i_, intercellular air spaces; _Fbv_, section of a +vein (fibrovascular bundle).] + +[Illustration: FIG. 224.—Chlorophyll bodies containing starch grains +in the course of formation. Magnified 250 times.] + +Sketch the section of your specimen as it appears under the +microscope. It will perhaps differ in some details from the one shown +in the figure, but you can recognize and label the corresponding +parts. Be sure that your drawing represents accurately the relative +size and shapes of the different kinds of cells. + +It is in the upper surface, where the chlorophyll particles abound, +that the manufacture of food goes on most actively, and from the +under surface, where the stomata are situated, that transpiration +takes place and air and other gases pass to and from the interior. +These facts have important bearings on the growth and external +characters of leaves. + + + Practical Questions + + 1. Explain why a plant cannot thrive if its stomata are clogged + with foreign matter. (179; Exp. 64; 184.) + + 2. Mention some of the ways in which this might happen. (181.) + + 3. Why must the leaves of house plants be washed occasionally to + keep them healthy? (179, 181.) + + 4. Why is it so hard for trees and hedges to remain healthy in a + large manufacturing town? + + + V. FOOD MAKING + + MATERIAL.—A sprig of pondweed, mare’s-tail (_Hippuris_), hornwort + (_Ceratophyllum_), marsh St.-John’s-wort (_Elodea_), or other green + aquatic plant; bean or tropæolum, or other green leaves gathered + from plants growing in the sunshine; a healthy potted plant; a + small, fresh cutting. + + APPLIANCES.—A shallow dish of water and two glass tumblers or + wide-mouthed jars; a bent glass or rubber tube; a piece of black + cloth or paper; a half pint of alcohol; iodine solution; a glass + funnel or a long-necked bottle from which the bottom has been + removed. + + EXPERIMENT 65. IS THERE ANY RELATION BETWEEN SUNLIGHT AND THE GREEN + COLOR OF LEAVES?—Place a seedling of oats, or other rapidly growing + shoot, in the dark for a few days, and note its loss of color. + Leave it in the dark indefinitely, and it will lose all color and + die. Hence we may conclude that there is some intimate connection + between the action of light and the green coloring matter of leaves. + + EXPERIMENT 66. DO LEAVES GIVE OFF ANYTHING ELSE BESIDES + WATER?—Submerge a green water plant, with the cut end uppermost, + in a glass vessel full of water, and invert over it a glass + funnel, or a long-necked bottle from which the bottom has been + removed as directed in Exp. 53. Expel the air from the neck of the + funnel—or bottle—by submerging and corking under water so as to + make it air-tight. Place in the sunlight and notice the bubbles + that begin to rise from the cut end of the plant. When they have + partly filled the neck of the funnel, remove the stopper and thrust + in a glowing splinter. If it bursts into flame, or glows more + brightly, what is the gas that was given off? (Exp. 22.) + + As oxygen is not a product of respiration, some other process must + be at work here, during which oxygen is set free, and some other + substance used up. (Exps. 24 and 25.) + +[Illustration: FIG. 225.—Experiment showing that green plants give +off oxygen in sunlight.] + +[Illustration: FIG. 226.—Experiment for showing that leaves absorb +carbon dioxide from the atmosphere.] + + EXPERIMENT 67. WHAT IS THE SUBSTANCE TAKEN IN WHEN OXYGEN IS GIVEN + OFF?—Fill two glass jars, or two tumblers, with water, to expel the + air, and invert in a shallow dish of water, having first introduced + a freshly cut sprig of some healthy green plant into one of them. + Then, by means of a bent tube, blow into the mouth of each tumbler + till all the water is expelled by the impure air from the lungs. + Set the dish in the sunshine and leave it, taking care that the + end of the cutting is in the water of the dish. After forty-eight + hours remove the tumblers by running under the mouth of each, + before lifting from the dish, a piece of glass well coated with + vaseline (lard will answer), and pressing it down tight so that no + air can enter. Place the tumblers in an upright position, keeping + them securely covered. Fasten a lighted taper or match to the end + of a wire, plunge it quickly first into one tumbler, then into the + other, and note the result. What was the gas blown from your lungs + into the jars? (Exps. 23, 24.) Why did the taper not go out in the + second jar? What had become of the carbon dioxide? + + EXPERIMENT 68. TO SHOW THAT LIGHT IS NECESSARY FOR A PLANT TO + ABSORB CARBON DIOXIDE AND GIVE OFF OXYGEN.—Repeat Exp. 66, keeping + the plant in a dark or shady place; do you see any bubbles? Test + with a glowing match; is any oxygen formed in the tube of the + funnel? Move back into the sunlight and leave for a few hours; what + happens when you thrust a glowing splinter into the tube? + + EXPERIMENT 69. IS ANY FOOD PRODUCT FOUND IN LEAVES?—Crush a few + leaves of bean, sunflower, or tropæolum, and soak in alcohol until + all the chlorophyll is dissolved out. Rinse them in water, and soak + the leaves thus treated in a weak solution of iodine for a few + minutes, then wash them and hold them up to the light. If there + are any blue spots on the leaves, what are you to conclude? If a + test for sugar is to be made, use sap pressed from fresh leaves; + for oils and fats, leaves should be dried without being placed in + alcohol. + +[Illustration: FIG. 227.—Leaf arranged with a piece of tin foil to +exclude light from a portion of the surface.] + + EXPERIMENT 70. HAS THE PRESENCE OR ABSENCE OF LIGHT ANYTHING TO DO + WITH THE OCCURRENCE OF STARCH IN LEAVES?—Exclude the light from + parts of healthy leaves on a growing plant of tropæolum, bean, + etc., by placing patches of black cloth or paper over them. Leave + in a bright window, or preferably out of doors, for several hours, + and then test for starch as in the last experiment; do you find any + in the shaded spots? + + EXPERIMENT 71. IS THE PRESENCE OF AIR NECESSARY FOR THE PRODUCTION + OF STARCH?—Cover the blades and the petioles of several leaves with + vaseline or other oily substance so as to exclude the air, and + after a day or two test as before. + +=185. Influence of plants on the atmosphere.=—These experiments +show that leaves cannot do their work without light and air. The +particular element of the atmosphere used by them in the process of +food making is carbon dioxide. Their action in absorbing this gas +and giving off oxygen tends to counterbalance the opposite action of +respiration, decomposition, and combustion of all kinds, by which the +proportion of it in the atmosphere tends to be constantly increased. +In this way they help to regulate the quantity of it present and have +a beneficial effect in ridding the air of one source of impurity. + +=186. Photosynthesis.=—In our examination of the internal structure +of the leaf, the chlorophyll bodies (184) were found to contain small +granules of starch which the chlorophyll, under the stimulus of +light, had elaborated as a nutriment for the plant tissues. Hence, +the leaf may be regarded as a factory in which vegetable food, +mainly starch, is manufactured out of the water brought up from the +soil, and the carbon dioxide derived through the stomata from the +atmosphere. In this process carbon dioxide (CO_{2}) is combined +with water (H_{2}O) in such proportions that part of the oxygen is +returned to the surrounding air. This is a fundamental food-forming +process characteristic of green plants, and can take place only in +the light. For this reason it has been named _Photosynthesis_, a word +which means “building up by means of light,” just as _photography_ +means “drawing or engraving by means of light.” + +In carrying on the operation of photosynthesis, sunshine is the +power, the chlorophyll bodies the working machinery, carbon dioxide +and water the raw materials, and starch or oil the finished product, +while oxygen and the water of transpiration represent the waste or +by-products. + +=187. How the new combination is effected.=—It may seem strange that +a gas and a liquid should combine to make something so different +from either as starch, but their chemical constituents are the same +in different proportions. Water is made up of 2 parts hydrogen and +1 part oxygen; carbon dioxide, of 1 part carbon and 2 parts oxygen, +while starch contains carbon, hydrogen, and oxygen, in the ratios of +6, 10, and 5, respectively. Hence, by taking sufficient quantities +of water and carbon dioxide and combining them in the proper +proportions, the leaf factory can turn them into starch. If we use +the letters C, H, and O, to represent Carbon, Hydrogen, and Oxygen, +respectively, the new combination of materials can be expressed by an +equation; thus:— + + _water_ _carbon dioxide_ _starch_ _by-products_ + 5(H_{2}O) + 6(CO_{2}) = (C_{6}H_{10}O_{5}) + 6(O_{2}) = 12(O). + +The water not used up in the process is given off as a waste product +in transpiration, while the oxygen is returned to the air, as shown +by Exp. 66. This equation is not to be understood as representing the +chemical changes that actually take place in the leaf. These are too +complicated, and at present too imperfectly known, to be considered +here. It will serve, however, to give a fair idea of the final result +from the process of photosynthesis, however brought about. + +Simple as the operation appears, the chemist has not, as yet, +been able to imitate it. He can analyze starch into its original +constituents, but while he has the ingredients at hand in abundance, +and knows the exact proportions of their combination, it is beyond +his power, in the present state of our knowledge, to put them +together. Hence, both man and the lower animals are dependent on +plants for this most important food element. The so-called factories +that supply the starch of commerce do not _make_ starch any more than +the miller makes wheat, but merely separate and render available for +use that already elaborated by plants. + +=188. Proteins.=—Foods of this class are mainly instrumental in +furnishing material for the growth and repair of the tissues out +of which the bodies of both plants and animals are built up. They +embrace a great variety of substances, but their chemical nature +is very complex and very imperfectly understood. Nitrogen is an +important element in their composition, whence they are commonly +distinguished as “nitrogenous foods.” Besides nitrogen, there are +present carbon, hydrogen, oxygen, and sulphur, and traces of the +mineral salts absorbed from the soil are found in varying quantities +in the ash of different proteins. The percentages in which these +ingredients are combined and the processes concerned in their +formation are at present a matter of pure hypothesis. Botanists +are not agreed even as to whether they are made in the leaf or in +some other part or parts of the plant, though the weight of opinion +inclines to the view that their construction takes place in the leaf. + +=189. The activities of leaves.=—As there are only 4 parts of CO_{2} +to every 10,000 parts of ordinary free air, it has been estimated +that in order to supply the leaf factory with the raw material it +needs, an active leaf surface of one square meter—a little over +one square yard—uses up, during every hour of sunshine, the CO_{2} +contained in 1000 liters (1000 quarts, approximately) of air. Suppose +an oak tree to bear 500,000 leaves, each having a surface of 16 sq. +cm., or 4 sq. in., and working 12 hours a day for 6 months in the +year; you will then have some idea of the enormous quantity of air +that passes each season through its leaf system. Add to this the +almost incredible volume of water transpired in the same time (180), +and we may well stand amazed at the tremendous activities of these +silent workers that we are in the habit of regarding as mere passive +elements in the general landscape. + +=190. The economic value of leaves.=—Besides their importance as +sanitary and food-making agencies, leaves have a direct commercial +value as food products in the hay and fodder they supply for our +domestic animals, the tea and salads with which they provide our +tables, the aromatic flavors and seasonings contained in them, and +the drugs, medicines, and dyes of various kinds for which they +furnish the ingredients. + + + Practical Questions + + 1. Why do gardeners “bank” celery? (Exp. 65.) + + 2. Why are the buds that sprout on potatoes in the cellar, white? + (Exp. 65.) + + 3. Why does young cotton look pale and sickly in long-continued wet + or cloudy weather? (Exp. 65.) + + 4. Why do parasitic plants generally have either no leaves or very + small, scalelike ones? (85, 186, 187.) + + 5. The mistletoe is an exception to this; explain why, in the light + of your answer to question 4. + + 6. Could an ordinary nonparasitic plant live without green leaves? + (186, 187.) + + 7. Are abundance and color of foliage any indication of the health + of a plant? (186, 187; Exp. 65.) + + 8. Is the practice of lopping and pruning very closely, as in the + process called “pollarding,” beneficial to a tree under ordinary + conditions? (186, 189; Exp. 63.) + + 9. Name some plants of your neighborhood that grow well in the + shade. + + 10. Compare in this respect Bermuda grass and Kentucky blue + grass; cotton and maize; horse nettle (_Solanun Carolinense_) and + dandelion; beech, oak, red maple, dogwood, pine, cedar, holly, + magnolia, etc. + + 11. Name all the aromatic leaves you can think of; all that are + used as food, beverages, drugs, and dyes. + + 12. What is the use of aromatic and medicinal leaves to the plant + itself? (Suggestion: Why does the housewife put lavender or tobacco + leaves in her woolen chest?) + + 13. Which would be richer in nourishment, hay cut in the evening or + in the morning, and why? (54, 186; Exp. 70.) + + 14. Mention three important sanitary services that are rendered by + a tree like that shown in plate 6 or 8. (180, 185, 189.) + + 15. Name some of the plants employed in the manufacture of starch. + + + VI. THE LEAF AN ORGAN OF RESPIRATION + + MATERIAL.—A number of vigorous, freshly cut green leaves; a liter + or two (one or two quarts) of expanding flower or leaf buds. + + APPLIANCES.—Some wide-mouthed jars of one or two liters’ capacity; + two small open vials of limewater. + + EXPERIMENT 72. DO LEAVES GIVE OFF CARBON DIOXIDE?—Cover the + bottoms of two wide-mouthed jars with water about two centimeters + (1 inch) deep. Place in one a number of healthy green leaves with + their stalks in the water, and insert among them a small open + vial containing limewater. In the other jar place only a vial of + limewater in the clear water at the bottom, this last being merely + to make the conditions in both vessels the same. Seal both tight + and keep together in the dark for about 48 hours, and then examine. + In which jar does the limewater indicate the greater accumulation + of CO_{2}? (It may show a slight milkiness in the other vessel + due to gas derived from the inclosed air and water.) From this + experiment, what process would you conclude has been going on among + the leaves in jar No. 1? (Exp. 25.) + +[Illustration: FIG. 228.—Arrangement of apparatus to show that heat +and carbon dioxide are given off by leaf buds.] + + EXPERIMENT 73. IS THE EXHALATION OF CARBON DIOXIDE ACCOMPANIED + BY ANY OTHER CONCOMITANT OF RESPIRATION?—In Exps. 24, 25, it was + shown that respiration is accompanied by heat; hence, if the + production of carbon dioxide by the leaf is due to this cause, it + should be attended by the evolution of heat. To find out whether + this is the case, partly fill a glass jar of two liters’ capacity + with unfolding leaf buds arranged in layers alternating with damp + cotton batting or blotting paper (Fig. 228); close the jar tightly + and leave from 12 to 24 hours in the dark to prevent the action + of photosynthesis. Then insert a thermometer and note the rise in + temperature. If a lighted taper is plunged in, it will quickly be + extinguished, showing that respiration has been going on. + +=191. Respiration in leaves.=—We see from experiments like the +foregoing that the leaf, besides carrying on the functions of +digestion, photosynthesis, and transpiration, is also an active agent +in the work of respiration. In this function oxygen is used up and +carbon dioxide given off, just as in the respiration of animals; but +the process is so slow in plants that it is much more difficult to +detect than the contrary action in photosynthesis, and is, in fact, +not perceptible at all while the latter is going on, though it does +not cease even then. + +But while the leaf is the principal organ of respiration, the process +is carried on in other parts of the plant as well, else it could not +survive during the leafless months of winter. It _appears_ to be most +active at night, but this is only because it is not obscured then, +as during the day, by the more active function of photosynthesis. +Indeed, it was for a long time supposed that plants “breathed” only +at night, and it was thought to be unwholesome to keep them in a +bedroom. It is now known, however, that respiration goes on at all +times and in all living parts of the plant, but the quantity of +oxygen taken in is so small from a hygienic point of view that it may +be disregarded. + +=192. Distinctions between respiration and photosynthesis.=—While +these two functions are contrasting and antipodal, so to speak, in +their action, they are mutually complementary and interdependent, the +one manufacturing food and the other using it up, or rather marking +the activity of those life processes by which it is used up. The +difference between them will be made clear by a comparison of the two +processes as summarized in the following statement: + + PHOTOSYNTHESIS RESPIRATION + + Goes on only in sunlight and in Goes on at all times and in all + the green parts of plants. parts of the plant. + + Produces starch and sugar. Releases energy (heat and working + power). + + Gives off, as by-product, oxygen. Gives off, as by-products, CO₂ + and water. + + A constructive process, in which A destructive, or consumptive + energy is used up to make food. process, in which food is used up + in expending energy. + +=193. Metabolism.=—The total of all the life processes of plants, +including growth, waste, repair, etc., is summed up under the general +term _metabolism_. It is a _constructive_ or building-up process when +it results in the making of new tissues out of food material absorbed +from the earth and air, and the consequent increase of the plant in +size or numbers. But, as in the case of animals, so with plants, not +all the food provided is converted into new tissue, part being used +as a source of energy, and part decomposed and excreted as waste. +In this sense, metabolism is said to be _destructive_. The waste in +healthy growing plants is always, of course, less than the gain, +and a portion of the food material is laid by as a reserve store. +For this reason, photosynthesis, being a constructive process, is +usually more energetic than respiration, which is the measure of the +destructive change of materials that attends all life processes. + +It is evident also, from what has been said, that growth and repair +of tissues can take place only so long as the plant has sufficient +oxygen for respiration, since the energy liberated by it is necessary +for the assimilation of nourishment by the tissues. + +Thus we see that plants are dependent on air not only for +respiration, but for nutrition, and none of their life processes can +be carried on without it. + + + Practical Questions + + 1. Can a plant be suffocated, and if so, in what ways? (87, 193; + Exps. 26, 27.) + + 2. The roots on the palm shown in plate 3 are not drawing any sap + from it as parasites; why does their continued growth bring about + the death of the tree? (87, 193.) + + 3. Is it unwholesome to keep flowering plants in a bedroom? Leafy + ones? Why, in each case? (191.) + + 4. Would there be any more reason for objecting to the presence of + flowers by night than by day? Explain. (191.) + + 5. Why is respiration much less marked in plants than in animals? + (30, 31.) + + + VII. THE ADJUSTMENT OF LEAVES TO EXTERNAL RELATIONS + + MATERIAL.—A potted plant of oxalis, spotted medick, white clover, + or other sensitive species. The subject is better suited for + outdoor observation than for laboratory work. + + EXPERIMENT 74. TO SHOW THAT LEAVES ADJUST THEMSELVES TO CHANGES IN + INTENSITY OF LIGHT.—Keep a healthy potted plant of oxalis, white + clover, or spotted medick in your room for observation. Note the + daily changes of position the leaves undergo. Sketch one as it + appears at night and in the morning. + +[Illustration: FIGS. 229, 230.—Leaves of a peanut plant: 229, in day +position; 230, in night position.] + + In order to determine whether these changes are due to want of + light or of warmth, put your plant in a dark closet in the middle + of the day, without change of temperature. After several hours note + results. Transfer to a refrigerator, or in winter place outside a + window where it will be exposed to a temperature of about 5° C. + (40° F.) for several hours, and see if any change takes place. Next + put it at night in a well-lighted room and note the effect. If + practicable, keep a specimen for several weeks in some place where + electric lights are burning continuously all night, and watch the + results. + + EXPERIMENT 75. TO SHOW THAT THE FALL OF THE LEAF MAY RESULT FROM + OTHER CAUSES THAN COLD OR FROST.—Wrap some leaves of ailanthus, + Kentucky coffee tree, ash, walnut, or hickory in a damp towel and + keep them in the dark for several days; the leaflets will fall + away, leaving a clear scar like those on winter twigs. + + EXPERIMENT 76. TO SHOW THAT ADJUSTMENTS TO TEMPERATURE MAY BE MADE + BY CHEMICAL MEANS.—Place a small twig of oleander, laurestinus, + or other broad-leaved evergreen in a 5 to 10 per cent solution of + sugar, and transfer it at the end of a few days to a temperature of + 6° to 8° below freezing. On comparison with a similar twig that has + stood for the same length of time in pure water, it will be found + to possess a greater power of resistance to cold. + +[Illustration: FIG. 231.—A plant that has been growing near an open +window, showing the leaves all turned toward the light.] + +=194. The light relation.=—The principal external conditions to which +leaves have to adjust themselves are light, air, moisture, gravity, +temperature, and the attacks of animals. From the knowledge of their +work and function gained in the preceding sections, it will be clear +that the primary relation of the leaf is a light relation, and to +this, first of all, it must adjust itself. + +It was shown in Exps. 56 and 57 how promptly leaves respond to +changes in the direction of light, and a little observation (Exp. +74) will convince us that they are equally sensitive to changes in +intensity and periodicity of illumination. + +=195. Phototropism.=—The movement of plants in response to light is +called _phototropism_—a word that means “turning toward or away from +light.” It includes all kinds of light adjustments, and examples of +it are to be met with everywhere in the disposition of leaves with +reference to their light exposure. + +=196. Horizontal and vertical adjustment.=—Take two sprigs, one +upright, the other horizontal, from any convenient shrub or tree—and +notice the difference in the position of the leaves. Examine their +points of attachment and see how this is brought about, whether by a +twist of the petiole or of the base of the leaf blades, or by a half +twist of the stem between two consecutive leaves, or by some other +means. + +[Illustration: PLATE 10.—A mosaic of moonseed leaves, showing +adjustment for light exposure. + +(_From_ Mo. Botanical Garden Rep’t.)] + +Observe both branches in their natural position; what part of the +leaf is turned upward, the edge or the surface of the blade? Change +the position of the two sprigs, placing the vertically growing one +horizontal, and the horizontal one vertical. What part of the leaves +is turned upward in each? + +[Illustration: FIGS. 232, 233.—Adjustment of leaves to different +positions: 232, upright; 233, procumbent.] + +[Illustration: FIG. 234.—Leaf mosaic of elm.] + +=197. Leaf mosaics.=—Trees with horizontal or drooping branches, +like the elm and beech, and vines growing along walls or trailing +on the ground, generally display their foliage in flat, spreading +layers, each leaf fitting in between the interstices of the others +like the stones in a mosaic, whence this has been called the _mosaic_ +arrangement. (Plate 10.) In plants of more upright or bunchy habit, +the leaves are placed at all angles, giving the appearance of a +rosette when viewed from above, whence this is called the _rosette_ +arrangement. + +A variety of the same disposition is seen in the pyramidal shape +assumed by plants with large, undivided leaves like the mullein and +burdock (Fig. 237), in which access of light is secured by a mutual +adjustment between the size and position of leaves, the upper ones +becoming successively smaller. + +=198. Heliotropism=—“turning with the sun”—is the name given to the +daily movement of plants like the cotton and sunflower in turning +their leaves or their blossoms to face the sun. If you live where +cotton is grown, notice the leaves in a field about ten o’clock on +a bright sunny morning, and again from the same point of view at +about four or five in the afternoon. Do you perceive any difference +in their general disposition? Watch on a cloudy day and see if any +change takes place. Find out by observation whether the “heliotrope” +of the hothouses is really heliotropic. + +[Illustration: FIGS. 235, 236.—Horse-chestnut leaves: 235, leaf +rosette seen from above; 236, the same seen sidewise, showing the +formation of rosettes by the lengthening of the lower petioles.] + +[Illustration: FIG. 237.—Leaf pyramid of mullein.] + +[Illustration: FIGS. 238, 239.—A compass plant, rosinweed (_Silphium +laciniatum_): 238, seen from the east; 239, seen from the south.] + +=199. Adjustment against too great intensity of light.=—Plants +frequently have to protect themselves against excess of light and +heat. An interesting example of this kind of adjustment is furnished +by the rosinweed, or compass plant (_Silphium laciniatum_, Figs. 238, +239), which grows in the prairies of Alabama and westward, where it +is exposed to intense sunlight. The leaves not only stand vertical, +but have a tendency to turn their edges north and south so that the +blades are exposed only to the gentler morning and evening rays. The +prickly lettuce manifests the same habit in a less marked degree. + +[Illustration: FIGS. 240, 241.—A plant of the guayule (_Parthenium +argentatum_), to the leaves of which indexes have been affixed to +show their day and night position: 240, day position; 241, night +position. (_From_ photographs by Prof. F. E. Lloyd.)] + +=200. Night and day adjustments.=—These are movements in response to +changes in the degree of illumination and temperature, as evidenced +by the fact that they become feeble and soon cease altogether if +the plant is kept a sufficient time under uniform conditions as +to these two factors. (Exp. 74.) They are called “nyctitropic” or +sleep movements, because they are most obvious in certain plants +that undergo periodic adjustments to the alternations of day and +night suggestive of an imaginary likeness to the sleep of animals. +Examples are most frequently met with among members of the pea +family (_Leguminosæ_), the spurges (_Euphorbiaceæ_), and the sorrel +(_Oxalis_) family. They are found among other species also, and +indeed are much more general than is usually supposed, most plants +showing signs of them if carefully tested. A simple way of doing +this is by attaching bristles about two inches long to the tips of +two leaves on opposite sides of the stem, as in Figs. 240, 241, +and comparing the divergence of the bristles during the day and at +nightfall. In this way a change of position in the leaves, too +slight to attract attention otherwise, will be made apparent. The +positions assumed vary in different plants, and even in the parts of +the same compound leaf; in the kidney bean, for instance, the common +petiole turns up at night, while the individual leaflets turn down. +One of the common pigweeds (_Amaranthus Palmeri_, Figs. 242-244) is +heliotropic in the day time and nyctitropic at night. + +[Illustration: FIGS. 242-244.—Showing the movements of _Amaranthus +Palmeri_: 242, 243, position at sunrise and sunset (heliotropic); +244, night position (nyctitropic) half an hour after sunset. (_From_ +photographs by Prof. F. E. Lloyd.)] + +The very striking nyctitropic adjustments of the wild senna (_Cassia +tora_) photographed by Professor Francis E. Lloyd of the Alabama +Polytechnic Institute (Figs. 245-250), though obviously influenced by +the sun, are not directed toward it as in those of truly heliotropic +plants. + +[Illustration: FIGS. 245-250.—Wild senna (_Cassia tora_), showing the +nyctitropic adjustments of its leaves. The upper figures show their +horizontal arrangement; those below, the vertical: 245, 248, position +of the leaves at 9 A.M.; 246, 249, at 3 P.M.; 247, 250, at 6.30 P.M. +(_From_ photographs by Prof. F. E. Lloyd.)] + +These movements are common also among flowers, many of them having +regular hours for opening and closing, as indicated by such names as +“morning-glory” and “four-o’clock.” In these cases, however, other +causes (277, 280) than the light relation must be taken into account. + +=201. Irritability= is a general term applied to the power in plants +of receiving and responding by spontaneous movements to impressions +from without. In its widest acceptation, irritability includes, +besides the various forms of adjustment described in this section and +the next, all movements due to geotropism, those of roots seeking +air and moisture, the revolution of twining stems and tendrils, +the circulation of protoplasm in the cell—any movement, in short, +that is made in response to an impression from the environment is a +manifestation of irritability. It may be of various degrees, but is +possessed to some extent by every living vegetable organism. + +The term is usually applied, however, more especially to those +obvious and pronounced responses made by plants to their +surroundings, as exemplified in the cases just given. Still more +marked instances are to be found in the movements of the tentacles +of insectivorous plants, and the sensitive leaflets of the mimosa +that close at the slightest touch. The tendrils of the passion flower +are said to appreciate and respond to a pressure that cannot be +distinguished even by the human tongue, and many plants will detect +and respond to the ultra-violet rays of light, which are entirely +invisible to man. + +This faculty of irritability among plants corresponds, in an +imperfect, rudimentary way, to what we recognize in animals as +nervous excitability. By this it is not meant to imply that the two +things are identical in their ultimate manifestations, though we +may regard them as fundamentally the same in that they are both to +be referred to the property inherent in protoplasm of responding to +stimuli. There is no indication, however, that irritability in the +vegetable kingdom is accompanied by anything like consciousness or +volition, or that plants possess any power of initiative. While the +movements in response to stimuli are in many cases eminently adapted +to a purpose, we have no evidence of a controlling power behind them. +The movement comes automatically in response to the stimulus, whether +the effect at the moment be advantageous or the reverse. + +=202. Adjustments in relation to moisture.=—These adjustments may +be—(1) To guard against excess of moisture; _e.g._ glands for +excreting water and salts; scales, wax, down, etc., on the surface of +leaves. These may serve also for protection against cold, insects, +excess of light and heat. (2) For the conservation of moisture; +_e.g._ the revolute leaf margins of grasses and sand plants growing +along the seashore; the fleshy leaves of stonecrops and purselanes; +the hard epidermis of yuccas and aloes; the scales, scurf, and down, +by which the moisture absorbed from the soil by plants growing in +dry and barren places is prevented from escaping too rapidly through +the stomata; the leaf cups and holders sometimes formed by winged +petioles and clasping leaf bases for retaining dew or rain water. +(3) For leaf drainage, or the conduction of moisture, by means of +grooves, channels, and taper-pointed leaves, which act as natural +gutters and drain pipes. + +[Illustration: FIG. 251.—Cross sections of the leaf of sand grass: +_a_, unrolled in its ordinary position; _b_ and _c_, rolled up to +prevent too rapid transpiration.] + +[Illustration: FIG. 252.—Winged petiole of _Polymnia_. FIG. +253.—Water cups of _Silphium perfoliatum_.] + +[Illustration: FIG. 254.—Fallen leaves. Notice how they cover the +ground with a warm mulch, protecting the soil from denudation, and +the roots and seeds from frost.] + +=203. The fall of the leaf.=—This is, in effect, an adjustment to +change of temperature, but that it is not directly due to cold is +shown by Exp. 75, and also by the fact that leaves in the tropics +and those of evergreens, while they do not fall at stated periods +like the bulk of the foliage in the temperate zones, are cut off just +the same and replaced by new ones, whenever, for any reason, they +are unable to perform their function. In cold climates they fall +at the approach of winter, not because the frost loosens them, but +because the roots are not able to absorb enough moisture to supply +them with material for making food. The needles and the scale-leaves +characteristic of evergreens in cold regions are enabled to persist +indefinitely by reason of their contracted surface. This prevents the +dissipation of moisture and affords no lodging for the accumulations +of sleet and snow that would otherwise cumber and perhaps break the +boughs with their weight. Trees and shrubs that shed their leaves +in winter are said to be _deciduous_, from a Latin word meaning “to +fall.” Can you mention some advantages of the deciduous habit to a +plant with broad, expanded leaves, growing in a cold climate? + +The mechanical means by which the leaf fall is accomplished is +through the growth of a corky layer of loose cells that forms at +the base of the petiole and cuts it away from the stem, leaving a +smooth, clean scar. Tear some fresh young leaves from a growing +twig and compare the scars with those on a winter bough. Do you see +any difference? This corky layer can be made to form in some plants +artificially, by depriving them of working material. (Exp. 75.) + +=204. The protection of wintergreen leaves.=—A great many, perhaps +the majority of broad-leaved evergreens, bear no obvious protection +against cold, while a large proportion, such as chickweed, violet, +fumitory, groundsel (_Senecio_), and dead nettle (_Lamium_), would +seem peculiarly unfitted, by their delicate structure, to withstand +it. But recent investigations by the Swedish botanist, Lidforss, +have shown that all wintergreen leaves, with the exception of those +on submerged water plants, which are sufficiently protected by the +medium in which they live, lose their starch in winter and contain +instead an increased percentage of sugar. The same is true of other +vegetable structures also, where starch is present, such as roots, +stems, tubers, and winter fruits—nuts, haws, persimmons, and the +like, which, as every schoolboy knows, become perceptibly sweeter +after frost. + +The presence of certain substances, of which sugar is the most +frequent, enables plants to withstand a greater degree of cold +than they could otherwise endure (Exp. 76). This effect, as shown +by Lidforss’s experiments, is due to the action of sugar in +counteracting, or retarding, the “salting out” of proteins by cold, +as explained in 33. + +As sugar is readily reconverted into starch by exposure to a +moderately high temperature for even a few days, we may find here +an explanation of the fact that plants which have survived the +prolonged cold of winter are often killed by a single sharp night +frost following a few warm days in early spring, before the tender +new growth has appeared. The plant suffers, not from the direct +effects of cold, but from the warmth preceding it, which stimulated +the transformation into starch of the sugar that would have prevented +the loss of proteins. On the same principle we may account for the +puzzling fact that the sunny southern side of trees and shrubs +usually suffers more from the effects of sudden frost than the shaded +and colder northern face. + +In apparent conflict with this reasoning is the fact that sugar +cane and the sugar beet are peculiarly susceptible to cold. This, +however, does not invalidate the premises established by Lidforss’s +researches, but merely emphasizes the need of further investigation, +which may either reconcile all the facts, or modify their +interpretation. + +=205. The colors of autumn leaves.=—These are due to the breaking +up and disappearance of the chlorophyll when the leaf factory has +to “shut down” for want of raw material to work with (203). It is +closely connected with the appearance of frost, since the same +changes of temperature which produce frost cause the cessation of sap +flow that brings about the disorganization of the chlorophyll and the +formation of various pigments derived from it. Besides these, leaves +may contain other coloring matters that are perceptible only when the +chlorophyll disappears; and in the sap there is a reddish pigment +which becomes either a very bright red, or a dark purplish maroon, +from the effect of chemicals that combine with it in the leaves. With +these coloring materials at command it is easy to see how the autumn +woods can assume such splendid hues. + + + Practical Questions + + 1. How would you explain the fact that the outer twigs of trees + generally are the most leafy? (99, 194; Exps. 57, 74.) + + 2. Is the common sunflower a compass plant? Is cotton? + + 3. Are there any such plants in your neighborhood? + + 4. Compare the leaves of half a dozen shade-loving plants of your + neighborhood with those of as many sun-loving ones; which, as a + general thing, are the larger and less incised? + + 5. Give a reason for the difference. (169.) + + 6. Why do most leaves—notably grasses—curl their edges backward in + withering? (182.) + + 7. What advantage is gained by doing this? (202.) + + 8. Observe such of the following plants as are found in your + neighborhood, and report any changes of position that may take + place in their leaves and the causes to which such changes should + be ascribed: wood sorrel, mimosa, honey locust, wild senna, + partridge pea, wild sensitive plant, redbud, bush clover, Japan + clover, Kentucky coffee tree, sensitive brier (_Schrankia_), + peanut, kidney bean. + + 9. Which of the trees named below shed their leaves from base to + tip of the bough (centripetally), and which in the reverse order: + ash, beech, hazel, hornbeam, lime, willow, poplar, pear, peach, + sweet gum, elm, sycamore, mulberry, China tree, sumac, chinquapin? + + 10. Account for the fact that evergreen trees and shrubs have + generally thick, hard, and shiny leaves, like those of the holly + and magnolia, or scales and needles, as the cedar and pine. (203.) + + 11. Why do many plants which are deciduous at the North tend to + become evergreen at the South? (203.) + + 12. Why are evergreens more abundant in cold than in warm climates? + (203.) + + 13. There is an apparent inconsistency between questions 11 and 12; + can you reconcile it? (203.) + + 14. Why is it more important to protect the south side of trees + against exposure to frost than the northern side? (33, 204.) + + 15. Explain why peach orchards on the tops and northern slopes of + elevated areas are less liable to have their fruit destroyed by + late frost than those in the valleys and on the southern slopes. + (33, 204.) + + + VIII. MODIFIED LEAVES + + MATERIAL.—Get from a florist a potted plant of sundew, + Venus’s-flytrap, sarracenia, or, if possible, one of all three, and + keep in the schoolroom for observation. The subject can be studied + best in a well-stocked greenhouse, if one is accessible. + +[Illustration: FIG. 255.—Spearlike leaves of Spanish bayonet.] + +=206. Modification and adaptation.=—Modification is structural +adjustment, or adaptation, carried so far as to obscure the original +form of an organ. Its true nature, however, can generally be +determined by some of the tests mentioned in 100. + +Examples of the modification of leaves to do the work of other +organs have already been noticed, as also their entire disappearance +in certain cases (97, 101, 149) and replacement by other parts; it is +unnecessary, therefore, to revert to this branch of the subject here. + +=207. Protective modifications.=—The most general protective +modifications that leaves undergo are (1) for the conservation +of moisture, as explained in 202, and (2) for protection against +animals. Many of the adaptations for the former purpose serve +incidentally for defense against animals also. Spines, hairs, scales, +sticky exudations, water holders, clasping and perfoliate leaves bar +the way to crawling insects; horny cuticles, as well as offensive +odors, bitter secretions, and poisonous juices warn leaf-eating +cattle and bugs away. These devices are merely protective, however, +and adapted to a passive attitude of self-defense. + +[Illustration: FIGS. 256-258.—Protective hairs magnified: 256, +mullein; 257, cinque-foil 258, Shepherdia.] + +=208. Insectivorous leaves.=—But sometimes a plant becomes the +aggressor, and instead of standing on the defensive or suffering +itself to be quietly devoured, proceeds to capture and devour small +game on its own account, and in this case, the leaf sometimes becomes +a deadly weapon of destruction. + +=209. Pitcher plants.=—The sarracenia, or trumpet leaf, is a +familiar example of this class. The lower part of the leaf blade is +transformed into a hollow vessel for holding water, and the top is +rounded into a broad flap called the _lamina_. Sometimes the lamina +stands erect, as in the common yellow trumpets of our coast regions, +and when this is the case, it is brilliantly colored and attracts +insects (Fig. 259). Sometimes, as in the parrot-beaked and the +spotted trumpet leaf, it is bent over the top of the water vessel +like a lid, and the back of the leaf, near the foot of the lamina, is +dotted with transparent specks that serve to decoy foolish flies away +from the true opening and tempt them to wear themselves out in futile +efforts to escape, as we often see them do against a window pane. + +[Illustration: FIG. 259.—Yellow trumpets (_Sarracenia flava_). +(_From_ the Mo. Botanical Garden Rep’t.)] + +[Illustration: FIG. 260.—Plant of sundew.] + +If the contents of one of these leaves are examined with a lens, +there will generally be found mixed with the water at the bottom the +remains of the bodies of a large number of insects. The hairs on the +outside all point up, toward the rim of the pitcher, while those on +the inside turn down, thus smoothing the way to destruction, but +making return impossible to a small insect when once it is ensnared. +When we remember that these plants are generally found in poor, +barren soil, we can appreciate the value to them of the animal diet +thus obtained. + +[Illustration: FIGS. 261-263.—Leaves of sundew magnified: 261, leaf +expanded; 262, leaf closing over captured insect; 263, leaf digesting +a meal.] + +=210. Flytraps.=—The most remarkable examples of insect-catching +leaves are the Venus’s-flytrap, found in the seacoast region of +North Carolina, and the sundew (_Drosera rotundifolia_), common +on the margins of sandy bogs and ponds. The latter is a delicate, +innocent-looking little plant, and owes its poetic name to the +dewlike appearance of a shining, sticky fluid exuded from glands on +its leaves, which glitter in the sun like dewdrops. It is, however, +a most voracious carnivorous plant, the sticky leaves acting as so +many bits of fly paper by means of which it catches its prey. When a +fly has been trapped, the tentacles close upon it, the edges of the +leaf curve inward, making a sort of stomach, from the glands of which +an acid juice exudes and digests the meal. After a number of days, +varying according to the digestibility of the diet, the blades slowly +unfold again and are ready for another capture. + +[Illustration: FIG. 264.—Bladderwort, showing finely dissected +submerged leaves bearing bladders for capturing animalculæ.] + +The bladderwort, common in pools and still waters nearly everywhere, +has its petioles transformed into floats, while the finely dissected, +rootlike blades bear little bladders which, when examined under the +microscope, are found to contain the decomposed remains of captured +animalculæ. + + + Practical Questions + + 1. Can you find any kind of leaf that is not preyed upon by + something? If so, how do you account for its immunity? + + 2. Make a list of some of the most striking of the protected leaves + of your neighborhood. + + 3. What is the nature of the protective organ in each case? + + 4. For protection against what does it seem to be specially adapted? + + 5. Are the plants in your list for the most part useful ones, or + troublesome weeds? + + 6. Examine the leaves of the worst weeds that you know of and see + if these will help in any way to account for their persistency. + + + Field Work + + (1) In connection with Sections I and II, observe the effect of the + lobing and branching of leaves in letting the sunlight through. + Notice any general differences that may appear as to shape, margin, + and texture in the leaves of sun plants, shade plants, and water + plants, and account for them. Study the arrangement of leaves on + stems of various kinds, with reference to the size and shapes of + leaves and their light relations. Consider the value of the various + kinds of foliage for shade; for ornament; as producers of moisture; + as food; as insect destroyers, etc. + + Make a special study of the twelve principal deciduous trees of + your neighborhood. Compare the leaves, bark, and branches of the + same trees so that you will be able to recognize them by any one of + these means alone. + + (2) In connection with Sections III and V, consider the effects + upon soil moisture of transpiration from the leaves of forest + trees and from those of shallow-rooted herbs and weeds that draw + their water supply from the surface. Consider the value of forests + in protecting crops from excessive evaporation by acting as wind + breaks. Study the effect of the fall of leaves upon the formation + of soil. In any undisturbed forest tract turn up a few inches of + soil with a garden trowel and see what it is composed of. Notice + what kind of plants grow in it. Note the absence of weeds and + account for it. Compare the appearance of trees scattered along + windy hillsides, where the fallen leaves are constantly blown away, + or in any position where the soil is unrenewed, with those in an + undisturbed forest, and then give an opinion as to the wisdom of + hauling away the leaves every year from a timber lot. + + (3) In Section VII, observe, in different kinds of leaf mosaics, + the means by which the adjustment has been brought about and the + purpose it subserves. Make a list of plants illustrating the two + habits. Notice the form and position of petioles of different + leaves, and their effect upon light exposure, drainage, etc., and + the behavior of the different kinds in the wind. Look for compass + plants in your neighborhood, and for other examples of adjustment + to heat and light. Study the position of leaves at different times + of day and in different kinds of weather and note what changes + occur and to what they are due. + + Make a list of ten plants that seem to you to have best worked out + the problem of leaf adjustment, giving the reasons for your opinion. + + Study the drainage system of different plants and observe whether + there is any general correspondence between the leaf drainage and + the root systems. This will lead to interesting questions in + regard to irrigation and manuring. Where plants are crowded, the + growth of both roots and leaves is complicated with so many other + factors that it is best to select for observations of this sort + specimens growing in more or less isolated situations. + + Notice the time of the expansion and shedding of the leaves of + different plants, and whether the early leafers, as a general + thing, shed early or late; in other words, whether there seems to + be any general time relation between the two acts of leaf expansion + and leaf fall. + + (4) Under Section VIII, look for instances of modified leaves; + study the nature of the different modifications you find, and try + to understand their meaning and object. Make a collection (_a_) + of all the leaves you can find modified to serve other than their + normal purposes; (_b_) of all the organs of other kinds that + have been modified to serve as leaves; (_c_) of all the modified + parts of leaves—stipules and petioles—that you can find. Keep the + collections separate, labeling each specimen with the name of the + plant it belongs to, what part it is, what use it serves, when and + where found. These collections need not be made individually, but + by the class as a whole and kept for the use of the school. + + Observe also (_d_) the differences between young and old leaves of + the same kind, and the leaves of young and old plants or parts of + plants of the same kind; (_e_) resemblances between young leaves + belonging to plants of different species; (_f_) between young + leaves of one species and mature ones of one or more different + species. Make a collection of all the specimens you can find + illustrating the three points mentioned, referring each to its + proper head, and giving the name and relative age—old or young—of + all specimens collected. + + + + +CHAPTER VII. THE FLOWER + + + I. DISSECTION OF TYPES WITH SUPERIOR OVARY + + MATERIAL.—For monocotyls, any flower of the lily family, + such as tulip, dogtooth violet (_Erythronium_), trillium, + star-of-Bethlehem, yucca, bear’s grass, and the like. The large + garden lilies make particularly good examples, but they are for the + most part spring bloomers. For autumn, spiderwort (_Tradescantia_), + arrow grass (_Sagittaria_), or late specimens of colchicum and + tiger lily may be used. Any of these will meet the essential + conditions of the analysis given in the text, but care should be + taken not to select for this exercise lily-like flowers of the iris + and amaryllis families, which have the _ovary inferior_. + + For examples of hypogynous dicotyls, flax, linden, pinks, + corn cockle, wood sorrel, poppies, tomato blossoms, and other + common flowers can usually be obtained without difficulty. In + autumn, the geraniums so largely cultivated for ornament will + meet all the conditions of the analysis. Specimens of the cress + family—wallflower, cabbage, mustard, turnip—can generally be found + everywhere and at all seasons, and they possess the advantage of + having their flowers throughout the order put up on so nearly the + same pattern that a description of one species will answer, even in + details, for the rest. + + For sympetalous specimens of the hypogynous type, hyacinth, lily of + the valley, bearberry, huckleberry, or other equivalent forms may + be used. + + APPLIANCES.—A compound microscope may be needed for examining + minute objects, such as pollen grains and ovules; but for all other + purposes, a good hand lens, with the pupil’s ordinary laboratory + equipment of drawing-materials, notebook, and dissecting needles, + will be sufficient for the studies outlined in this and the four + succeeding sections. + +[Illustration: FIGS. 265-267.—Flower of a monocotyl +(star-of-Bethlehem), with superior ovary dissected: 265, entire +flower, showing the different sets of organs: _pet_, petals; _sep_, +sepals; _sta_, stamens; _pist_, pistil; _ped_, peduncle; 266, side +view with all the petals and sepals but two removed to show order +of the parts: _r_, receptacle; _o_, ovary; _sty_, style; _stig_, +stigma—parts composing the pistil; _f_, filament; _a_, anther—parts +composing the stamen; 267, cross section of the ovary: _c_, _c_, +carpels; _ov_, ovules; _pl_, placenta.] + +=211. The floral envelopes.=—Make a sketch of your specimen flower +from the outside. Is it solitary, or one of a cluster? If the latter, +refer to 160-162 and tell the nature of the cluster. Notice the +color; is it conspicuous enough to attract attention or not? Can this +have anything to do with its clustered or solitary position? Label +the head of the peduncle that supports the flower, _receptacle_; +the outer greenish leaves, _sepals_; the inner, lighter-colored +ones, _petals_. The sepals taken together form the _calyx_, and the +petals, the _corolla_. Where the petals and sepals are all separate +and distinct, as in the tulip and the star-of-Bethlehem, the corolla +is said to be _polypetalous_ and the calyx _polysepalous_, words +meaning, respectively, many-petaled and many-sepaled. _Monopetalous_ +and _monosepalous_, or _sympetalous_ and _synsepalous_, are terms +used to describe a condition in which the petals or sepals are all +united into one, as in the morning-glory and lily of the valley. In +many flowers, there is little or no difference between the two sets +of organs. In such cases the calyx and corolla together are called +the _perianth_, but the distinction of parts is always observed, the +outer divisions being regarded as sepals, the inner ones as petals. +These two sets of organs constitute the _floral envelopes_, and are +not essential parts of the flower, as it can fulfill its office +of producing fruit and seed without them. Note their number, mode +of attachment to the receptacle, and how they alternate with each +other. Remove one of the sepals and one of the petals, and notice +any differences between them as to size, shape, or color. Which is +most like a foliage leaf? Hold each up to the light and try to make +out the veining. Is it the same as that of the foliage leaves? If a +light-colored flower is used, examine a specimen that has stood in +coloring fluid. How many of each set are there? + +[Illustration: FIGS. 268-269.—Yucca blossom: 268, external view: +_br_, bract; _pd_, peduncle; _r_, receptacle; _s_, sepal; _pet_, +petal; 269, vertical section: _ped_, peduncle; _br_, bract; _r_, +receptacle; _per_, perianth; _sta_, stamen; _o_, ovary; _sty_, style; +_stg_, stigma. The last three parts named compose the pistil.] + +[Illustration: FIGS. 270-274.—Stamens: 270, a typical stamen with the +terminal anther, _b_, surmounting the filament, _a_, and opening in +the normal manner down the outer side of each cell; 271, stamen of +tulip tree, with adnate extrorse anther; 272, stamen of an evening +primrose (_Œnothera_) with versatile anther; 273, stamen of pyrola, +the anther cells opening by chinks or pores at the top; 274, stamen +of a cranberry, with the anther cells prolonged into a tube and +opening by a pore at the apex. (_After_ GRAY.)] + +=212. The essential organs.=—Next sketch the flower on its inner +face, labeling the appendages just within the petals, _stamens_, +and the central organ within the ring of stamens, _pistil_. These +are called essential _organs_ because they are necessary to the +production of fruit and seed. Note their mode of insertion, three of +the stamens in a flower like the star-of-Bethlehem alternating with +the petals, and the other three with these and with the lobes of the +base of the pistil. + +=213. The stamens.=—Notice whether the stamens are all alike, or +whether there are differences as to size, height, shape, color, etc. +Do these differences, if there are any, occur indiscriminately and +without order, or in regular succession between the alternating +stamens? Examine one of the little powdery yellow bodies at the tip +of the stamens, and see whether they face toward the pistil or away +from it. + +Remove one of the stamens and sketch as it appears under the lens, +labeling the powdery yellow body at the top, _anther_, and the +stalklike body supporting it, _filament_. Usually the filaments +are threadlike, whence their name, but sometimes, as in the +star-of-Bethlehem, they are flattened and look like altered petals. +See if you can find such a one. What would you infer from this fact +as to the possible origin of the stamens? (100.) + +[Illustration: FIGS. 275-278.—Forms of pollen: 275, from _mimulus_; +276, star cucumber; 277 wild balsam apple; 278, _hibiscus_. (_After_ +GRAY.)] + +Notice the two little sacs or pouches that compose the anther, as to +their shape and manner of opening, or dehiscing, to discharge the +powder contained in them. This powder is called _pollen_, and will +be seen under the lens to consist of little yellow grains. These are +of different shapes, colors, and sizes, in different plants, and +their surface often appears beautifully grooved and striate when +sufficiently magnified. Place some of the pollen under the microscope +and draw two of the grains, with their markings. In the hibiscus and +others of the mallow family, they are large enough to be seen with a +hand lens. + +=214. The pistil.=—Remove the stamens and sketch the pistil as it +stands on the receptacle. Label the round or oval enlargement at +the base, _ovary_, the threadlike appendage rising from its center, +_style_, and the tip end of the style, _stigma_. In some specimens +the style may be very short, or wanting. In this case the stigma is +_sessile_, and the pistil consists of stigma and ovary alone. If the +stigma is lobed or parted, count the divisions and see if there is +any correspondence between them and the number of petals and sepals, +or of the lobes of the ovary. Examine the tip with a lens and notice +the sticky, mucilaginous exudation that moistens it. Can you think of +any use for this? If not, touch one of the powdery anthers to it, and +examine it again with a lens. What do you see? Can you blow or dust +the pollen from the stigma? + +=215. Pollination=, or the transfer of pollen from the anther to +the stigma, is a matter of great importance, as the pistil cannot +develop seed without it, except in the case of a few plants like the +Alpine everlasting, some species of meadow rue (_Thalictrum_), and +_Alchemilla_, which have the unusual faculty of perfecting seeds in +the absence of pollen. Note the relative position of pistils and +stamens and see if it is such that the pollen can reach the stigma +without external agency. + +=216. The ovary.=—Observe the shape of the ovary, and the number of +ridges, or grooves, that divide the surface. Select a flower which +has begun to wither, so that the ovary is well developed, cut a cross +section near the middle, and try to make out the number of _locules_, +or internal divisions. Do you perceive any correspondence in number +between these and the ridges or lobes outside (Fig. 280)? Between +them and the lobes of the stigma? The walls that inclose the cavities +of the ovary are called _carpels_, and the ridges or depressions that +mark their point of union on the outside are the _sutures_, or seams. +The little round bodies in the locules, as the compartments of the +ovary are called, are the _ovules_, which will later be developed +into seeds. Their place of attachment is the _placenta_. If they are +attached to the walls of the carpels (Fig. 281), the placenta is +_parietal_; if to a central axis formed by the edges of the carpels +projecting inwards (Fig. 282), it is central and axial; if instead of +being attached to the carpels, the ovules are borne on a projection +from the receptacle, the placenta is a _free central_ one (Fig. 283). +If your cross section shows a central placenta, make a vertical cut +down to the receptacle and find out whether it is free, or axial. +What appears to be the primary office of the ovary? Make an enlarged +sketch of your specimen in both vertical and horizontal section, +labeling correctly all the parts observed. + +[Illustration: FIGS. 279, 280.—Ovary of yucca, a hypogynous +monocotyl, dissected: 279, vertical section; _ov_, ovules; 280, +diagram of a horizontal section of the same, enlarged, showing the +three carpels and six locules; _ds_, dorsal sutures; _vs_, ventral +sutures; _ov_, ovules; _pl_, placenta.] + +[Illustration: FIGS. 281-283.—Different kinds of placenta: 281, +parietal; 282, central and axial; 283, free central. 281 and 282 are +horizontal sections; 283, vertical.] + +[Illustration: FIG. 284.—Horizontal diagram of a flower of the lily +kind. The dot represents the growing axis of the plant.] + +=217. Numerical plan.=—Make a horizontal diagram of the plan of the +whole flower, after the model given in Fig. 284, showing the order +of attachment of the different cycles,—sepals, petals, stamens, +and pistils,—the number of organs in each set, and their mode of +alternation with the organs of the other cycles. Notice that the +parts of each set are in threes, or multiples of three. This is +called the numerical plan of the flower, and is the prevailing number +among monocotyls. It is expressed in botanical language by saying +that the flower is _trimerous_, a word meaning measured, or divided +off, into parts for three. + +=218. Vertical order.=—Next make a vertical diagram of your specimen +after the manner shown in Fig. 269, and note carefully that the +ovary stands _above_ the other organs (this is true of all the lily +family), and is entirely separate and distinct from them. In such +cases the ovary is said to be _free_, or _superior_, and the other +organs _inferior_, or _hypogynous_, a word meaning “inserted under +the pistil.” These terms should be remembered, as the distinction is +an important one in plant evolution. + +=219. Summary of observations.=—In the flower just examined, we +found that there were four sets of floral organs present—sepals, +petals, stamens, and pistil; that the individual organs in each set +were alike in size and shape; that there were the same number, or +multiples of the same number of parts in each set, and that all the +parts of each set were entirely separate and disconnected, the one +from the other, and from those of the other cycles. Such a flower is +said to be:— + +_Perfect_, that is, provided with both kinds of organs essential to +the production of seed—stamens and pistil. + +_Complete_, having all the kinds of organs that a flower can have: +viz. two sets of essential organs, and two sets of floral envelopes. + +_Symmetrical_, having the same number of organs, or multiples of the +same number, in each set. + +_Regular_, having all the parts of each set of the same size and +shape, as in the wild rose and bellflower, or if different, arranged +in regular order or pairs, so that there will be a correspondence +between the two sides of the flower, as in the violet, sweet +pea, sage, and larkspur. For convenience, the two kinds may be +distinguished as _complete_ and _bilateral regularity_, respectively. + +The opposites of these terms are: _imperfect_, _incomplete_, +_asymmetrical_ or _unsymmetrical_, and _irregular_. + +Note that regularity refers to form, symmetry to number of parts, and +that a flower may be perfect without being complete. + +[Illustration: FIGS. 285-288.—A flower of the cress family: 285, +side view; 286, view from above; 287, diagram of parts: _p_, petals; +_s_, sepals; _st_, stamens; _pi_, pistil; _cl_, claw of petal; +, +, +position of the missing stamens; 288, pistil and stamens, enlarged. +(_After_ GRAY.)] + +[Illustration: FIG. 289.—Section of a tomato flower, showing the +hypogynous arrangement: _cx_, calyx; _c_, corolla; _s_, stamens; _p_, +pistil; _o_, ovary; _st_, stigma. (Twice natural size.)] + +=220. Dissection of a typical dicotyl flower.=—(Poppy, flax, pink, +tomato, linden, etc., can be substituted for the specimen used in +the text.) Gently remove the sepals and petals from a wallflower, +stock, mustard, or other cress flower, lay them on the table before +you in exactly the order in which they grew on the stem, and sketch +them. How many of each are there, and how do they alternate with +one another? Sketch the pistil and stamens as they stand on the +receptacle; how many of the latter are there? Notice that two of the +six are outside and a little below the others, alternate with the +petals, while the other four stand opposite them, as is natural, +if they were alternating with another ring of stamens between +themselves and the corolla. Put a dot before two of the sepals in +your first drawing to indicate the position of the two outer stamens, +and a cross before the other two to show where stamens are wanting +to complete the symmetry of this set, as in Fig. 287. When parts +necessary to complete the plan of a flower are wanting, as in this +case, they are said to be _obsolete_, _suppressed_, or _aborted_. +Place dots before the petals to represent the other four stamens. +Sketch one of the anthers as it appears under a lens, showing the +arrow-shaped base, and the mode of attachment to the filament. Is it +such that the pollen can reach the stigma without external agency? In +what manner do the anthers open to discharge their pollen? Are the +anthers and stigma mature at the same time? Remove all the stamens +from a flower and sketch the pistil, showing the long, slender +ovary, the very short style, and the _capitate_ (that is, round +and knoblike) stigma. Make cross and vertical sections of one of +the older pistils lower down on the stem. How many ovules does it +contain? How are they attached? Represent the position of the pistil +by a small circle in the center of your sketch of the separate parts. +You have now a complete ground plan of the flower. Diagram a vertical +section, as in Fig. 289, showing the position of the ovary with +reference to the other parts, and report in your notebook as to the +following points:— + + Numerical plan Presence or absence of parts + Symmetry Union of parts + Regularity (complete or bilateral) Position of ovary + + + + + II. DISSECTION OF TYPES WITH INFERIOR OVARY + + MATERIAL.—For monocotyls: in spring and early summer, iris, + snowflake, freesia, crocus, narcissus, daffodil, can be used; + in autumn, gladiolus, blackberry lily, fall crocus, star grass + (_Hypoxys_). For dicotyls: in spring, flowers of apple, pear, + quince, gooseberry, squash, gourd, melon (with both male and female + flowers); in late summer and autumn, fuchsia, evening primrose + (_Œnothera_), willow-herb (_Epilobium_). + +=221. Study of a monocotyl flower.=—Compare with the specimens +examined in the last section, a narcissus, snowflake, or iris flower. +What difference do you notice in the position of the ovary? Would +you call it _inferior_ (below the other parts) or _superior_ (above +them)? How was it in the lily and the hyacinth? If your specimen +is an iris, notice that it is sessile in the axil of a large bract +called a _spathe_, which conceals the lower part of the flower. +Remove the spathe and observe that the lower part of the perianth is +united into a long, narrow tube, from the top of which the sepals and +petals extend as long, curving lobes. + +[Illustration: FIG. 290.—Iris flower: _sp_, spathes; _s_, sepals + +_p_, petals = perianth.] + +[Illustration: FIG. 291.—Vertical section of iris flower: _ov_, +ovules; _pl_, placenta; _tu_, tube of the perianth inclosing the +style; _sta_, stamen; _sti_, stigma: _o_, ovary. (_After_ GRAY.)] + +[Illustration: FIG. 292.—Vertical section of iris flower, with +perianth removed, showing a stamen and three stigmas: _su_, stigmatic +surface.] + +[Illustration: FIG. 293.—Cross section of ovary of iris flower: _c_, +_c_, carpels; _l_, _l_, locules; _ov_, ovules; _pl_, placenta.] + +=222. Arrangement of parts.=—Sketch the outside of the flower, +labeling the oblong, three-lobed enlargement at the base, _ovary_; +the prolongation above it, _tube of the perianth_; the three outer +lobes with the broad sessile bases, _sepals_; the others, with +their bases narrowed and bent inward, _petals_. Now turn the flower +over and sketch the inside, labeling the three large, petal-like +expansions in the center, _stigmas_. Do you see any stamens? Remove +one of the sepals and look under the stigma; what do you find there? +Notice the little honey pockets at the foot of the stamen. Run the +head of your pencil into them and see what would happen to the head +of an insect probing for honey. + +Remove the perianth and sketch the remaining organs in profile, +showing the position of the stamens. Do you see any advantage in +their position? Can you determine the use of the crest of hairlike +filaments on the upper side of the sepals? Remove a stamen and sketch +it. + +=223. The pistil.=—Remove as much of the upper part of the perianth +tube as you can without injuring the pistil, and with a sharp knife +cut a vertical section down through the ovary so as to show the long +style and its connection with the placenta. Make a sketch of this +longitudinal section (see Fig. 291), labeling the parts observed. +Notice whether the placenta is central or parietal. Draw a cross +section of the ovary; how many locules has it? How many ovules in +each? Where are they attached? Is the placenta free central or axial +(Fig. 293)? Examine with a lens the little flap at the base of the +two-cleft apex of one of the stigmas, and look for a moist spot to +which the pollen will adhere. Label this in your sketch, _stigmatic +surface_. No seeds can be matured unless some of the pollen reaches +this surface; can you think by what agency it is carried there? What +insects have you seen hovering about the iris? Notice that in drawing +his head _out_ of the flower, an insect would not touch the stigmatic +surface, since it is on the _upper_ side of the flap and he would be +probing _under_ it. But in entering the next flower that he visits, +he is likely to strike his head against the flap and turn it under, +thus dusting it with pollen brought from another flower. + +[Illustration: FIG. 294.—Horizontal diagram of iris flower.] + +=224. Diagrams.=—Draw diagrams showing the horizontal and vertical +arrangement of parts in the iris or other specimen examined, and +compare with those made of the monocotyl studied in the preceding +section. In what respect does it differ from them? How do you account +for the difference in the number of stamens, if there is any? (220.) + +=225. The vertical order.=—The difference in vertical arrangement is +an important one. Bear in mind that flowers of this type have the +ovary _inferior_, that is, inserted _under_ the other organs (Figs. +296, 304), which are then said to be superior, or _epigynous_, a word +which, as you know from the prefix _epi_ (47), means over or above +the pistil. To make the matter clear, the two sets of terms employed +for describing the position of the ovary are given below in parallel +columns: + + Hypogynous Epigynous + Ovary superior Ovary inferior + Calyx or perianth inferior Calyx or perianth superior + +The epigynous arrangement is considered as marking a higher stage of +floral development than the hypogynous, which is characteristic of a +more simple and primitive structure. + +[Illustration: FIGS. 295-296.—Evening primrose, dicotyl flower with +inferior ovary: 295, exterior view; 296, longitudinal section, +showing vertical arrangement of parts.] + +=226. Dissection of a dicotyl flower.=—Sketch a blossom of quince +or apple, fuchsia, evening primrose, etc., first from the outside, +then from the inside, and then in vertical section, labeling the +parts as in your other sketches. Notice in the pear or apple how the +ovary is sunk in the hollowed-out receptacle. Where are the other +parts attached? Are they inferior or superior? Hold up a petal to the +light and examine its venation through a lens. (Use for this purpose +a petal from a flower that has stood in red ink for two or three +hours.) Is it parallel-veined or net-veined? If the flowers are +clustered, what is the order of inflorescence? Does the position of +the flowers on their branch correspond to that of the leaf axils on +the same kind of plant? + +[Illustration: FIGS. 297-300.—Flower and sections of pear: 297, +cluster of blossoms, showing inflorescence; 298, vertical section +of a flower; 299, ground plan of a flower; 300, vertical section of +fruit.] + +[Illustration: FIG. 301.—Vertical section of an almond blossom with +petals removed, showing the perigynous arrangement.] + +=227. The stamens.=—Remove the petals from a flower and examine +the stamens with a lens. Notice the attachment and shape of the +anthers. Are they all of the same color? How do you account for +the difference, if there is any? Is the position of the pistil and +stamens such that the pollen from the anthers can readily reach +the stigmas without external aid? Examine the pistil in flowers of +different ages, and see if the stigma is mature (that is, moist and +sticky) at the same time that the anthers are discharging their +pollen. Make an enlarged sketch of a stamen showing the shape of the +anther and the method of opening to discharge pollen. + +=228. The pistils.=—How many pistils do you find in the apple blossom +(or other flower under examination)? Are they distinct, or united? +Find where the styles originate; what do you see there? Make a cross +section of the ovary and count the locules; how does their number +compare with that of the styles? Can you make out the number of +ovules in each? If not, use a young fruit; as it is only an enlarged +ovary, it will show the parts correctly. Compare it with a ripe fruit +and see if all the ovules matured. Can you think of any reasons why +some of them might fail? Do you see any signs of nourishment stored +in the ovary? Name all the ways you can think of in which the ovary +can benefit the ovules and seeds. Draw the ovary in cross and +vertical sections, labeling correctly all the parts. + +[Illustration: FIGS. 302-304.—Diagrams showing arrangement of parts +with reference to the ovary: _bd_, receptacle; _k_, calyx; _kr_, +corolla; _st_, stamens; _fr_, ovary; _g_, style; _n_, stigma; 302, +perigynous; 303, hypogynous; 304, epigynous.] + +=229. The numerical plan of dicotyls.=—Diagram the plan of the flower +in cross and vertical section. How many parts are there in each set? +Can you tell readily the number of stamens? When the individuals of +any set or cycle of organs are too numerous to be easily counted, +like the stamens of the apple, pear, and peach, or the petals of the +water lily, they are said to be _indefinite_. It is very seldom that +perfect symmetry is found in all parts of the flower. The stamens and +pistil, in particular, show a great tendency to variation, so that +the numerical plan is generally determined by the calyx and corolla. +Where the parts are in fives, as in the pear, quince, and wild rose, +the flower is said to be _pentamerous_, or in sets of five. This is +the prevailing number among dicotyls, though other orders are not +uncommon. In the mustard family (220) and other well-known species, +the fourfold order prevails, while some of the saxifrages have their +parts in twos, and the magnolia and the pawpaw have a threefold +arrangement. + +=230. Intermediate types.=—Flowers like the peach and rose represent +an intermediate type in which the calyx, petals, and stamens are +attached to a prolongation of the receptacle that extends above the +ovary, but is not united with it (Fig. 301). In general, a flower is +not considered as belonging to the epigynous kind unless the ovary is +more or less consolidated with the parts around it (Fig. 304). + + + III. STUDY OF A COMPOSITE FLOWER + + MATERIAL.—The largest heads attainable should be selected, as the + florets are small at best, and difficult to handle. The large + cultivated sunflower (_Helianthus annuus_) makes an ideal specimen, + if accessible. Oxeye daisy and dandelion can be obtained throughout + the season almost everywhere, but the former has no pappus, and + the latter does not show the tubular disk flowers. Other common + specimens are: for spring, mayweed, Jerusalem artichoke, coreopsis, + arnica; for late summer and autumn, China aster, golden aster + (_Chrysopsis_), sneezeweed, elecampane—and, in fact, the great + majority of flowers to be found at this season are of the composite + family. Oxeye daisy is used as a model in the text on account of + its general accessibility, but almost any specimen of the radiate + kind will meet all essential conditions of the analysis. + +[Illustration: FIGS. 305-308.—An oxeye daisy: 305, a flower head; +306, vertical section of a head; 307, disk flower; 308, ray flower, +enlarged.] + +=231. The ray flowers.=—Examine the upper side of an oxeye daisy +through a lens. Of what is the yellow button in the center composed? +Count the narrow, petal-like rays disposed around the center. To +decide what they are, look for a small two-cleft body at the base of +the ray; this is the pistil. Do you see any stamens in the ray? An +examination will show that all rays contain pistils, but no stamens; +they are, therefore, not petals, but the corollas of imperfect +flowers. Look at the upper edge of a ray of sneezeweed, coreopsis, +arnica, chicory, etc., for small teeth or notches; these represent +the lobes of a sympetalous corolla. Split one of the tubular corollas +of the disk down one side and open it out flat; does it throw any +light on the morphology of the ray? In many composite plants, as the +sunflower, coneflower, coreopsis, the rays are all _neutral_; that +is, they have neither pistil nor stamens. Are they of any use in such +cases? If you are in doubt, remove all the rays from a head; would +the disk be noticeable enough to attract attention without them? What +is the principal office of the rays? + +=232. The involucre.=—Look at the cluster of green, leafy scales on +the under side of the head. It is not a calyx, but a collection of +bracts, called an _involucre_. Have you ever noticed the bracts under +the separate flowers on a raceme? (161.) What would be the position +of the bracts if all the flowers of the raceme were compacted into a +head like the daisy or sunflower? Is the involucre of any use? Cut +it away gently so as not to disturb the other organs and see what +happens to the rays. + +=233. The disk flowers.=—Cut a vertical section through the head of a +flower and notice the broad, flat receptacle (in some cases round or +columnar) on which the tiny florets are seated. Observe whether it is +naked, or whether it bears chaffy scales inclosing the florets. Make +an enlarged drawing of this section, showing the insertion of the +different parts and labeling them all correctly. What differences do +you observe between the disk and the ray flowers? + +=234. The pappus.=—Open one of the disk flowers with a dissecting +needle and observe the small striate (in some specimens, hairy) +body to which the base of the style is attached. This is the +ovary, inclosed in the lower part of the calyx, which has become +incorporated with it. When mature, it will form a small, one-seeded +fruit called an _akene_. Can you see the ovule? Where is it +attached? (Use a mature akene for this purpose.) In most plants of +this family, the akene is surmounted by delicate hairy bristles, +as in the dandelion, wild lettuce, and groundsel; or by small +chaffy scales, as in the sneezeweed and sunflower, and sometimes by +hooks and barbed hairs, like those of the tickseed, bur marigold, +and cocklebur. These appendages constitute the _pappus_. They are +modifications of the sepals, and serve an important purpose in aiding +the distribution of the seed. Can you suggest some of the ways in +which they may aid in accomplishing this object? + +[Illustration: FIGS. 309-314.—Akenes of the composite family: +309, mayweed (no pappus); 310, chicory (pappus a shallow cup); +311, sunflower (pappus of two deciduous scales); 312, sneezeweed +(_Helenium_, pappus of five scales); 313, sow thistle (pappus of +delicate downy hairs); 314, dandelion, tapering below the pappus into +a long beak. (_After_ GRAY.)] + +[Illustration: FIGS. 315-317.—Flowers of _Arnica montana_, showing +successive stages in pollination: 315, pistil just extruding from +anther tube, covered with pollen, but with stigmatic surfaces closed; +316, stigma opened and mature; 317, stigma recurved to receive pollen +from its own or neighboring anthers if foreign pollen has not reached +it.] + +=235. The stamens and pistil.=—Remove the corolla of a disk flower +carefully so as not to disturb the inclosed organs, and notice how +the stamens are united into a tube by their anthers. Flatten out the +tube and make an enlarged sketch of it, showing the long, narrow +shape of the anthers and their mode of attachment. Can you make out +how they open to discharge their pollen? Examine one of the younger +florets near the center of the disk, and observe that the tip of the +style is inclosed in the anther tube with the lobes of the stigma +pressed tightly together by their inner faces (Fig. 315), so that it +is impossible for any of the pollen to reach the stigmatic surface. +It remains in this position till the anthers have shed their pollen, +then, as may be seen by examining an older flower, the style begins +to elongate, pushing up the pollen that has fallen on the hairy +outside of the closed stigma, and forcing it out of the corolla tube, +where it can be scattered by insects among the other flowers of the +cluster. When the pollen of its own floret has been thus disposed of, +the stigma lobes open and curl outward, ready to receive the pollen +from other flowers. This arrangement is practically universal among +plants of the composite family; can you divine its object? It will be +shown later, that much larger and stronger seeds are produced when +the pistil is pollinated from a different flower, or, better still, +from a different plant of the same species; hence, you see what a +useful adaptation this is. + +=236. Nature of a composite flower.=—It will be evident, from the +examination just made, that the daisy, dandelion, sunflower, etc., +are not single flowers, but compact heads of small blossoms so +closely united as to appear like a single individual; hence they +are said to be _composite_, or compound. They are the most numerous +and widely disseminated of all plants, comprising one seventh of +the entire flowering vegetation of the globe, and are regarded +by botanists as representing the most advanced stage of floral +evolution. Can you point out some of the adaptations to which their +success in solving the problems of plant life is due? (164.) + + + IV. SPECIALIZED FLOWERS + + MATERIAL.—For spring and early summer: sweet pea, black locust, + wistaria, lupine, or any of the characteristic butterfly-shaped + flowers of the pea family. For autumn or late summer: tropæolum, + monkshood, or a bilabiate flower—snapdragon, digitalis, dead + nettle, salvia, catalpa, etc.—of the mint or figwort family. + +=237. Irregularity and specialization.=—Irregularity and bilateral +regularity are, as a rule, indicative of specialization, or +adaptation to a particular purpose, such as the ready distribution +of pollen, or its protection against injury. These adaptations +are more noticeable in the corolla than in other parts, and hence +flowers of this kind are usually classed according to the shape of +their corollas. The most highly specialized flowers in this respect +are the orchids, but they are too rare and difficult of access +to be available objects for study. The most familiar and widely +distributed kinds of specialized corollas are the _bilabiate_, or +two-lipped, and the _papilionaceous_, or butterfly, forms. The +first is characteristic of the mint and figwort families, of which +the toadflax, sage, and catalpa are familiar examples. The second +comprises the well-known papilionaceous flowers of the pea family, +named from the Latin word _papilio_, a butterfly, on account of their +general resemblance to that insect. + +=238. Dissection of a papilionaceous flower.=—Sketch a blossom of any +kind of pea or vetch as it appears on the outside. Are the sepals +all of the same length and shape? If not, which are the shorter, the +upper or the lower ones? + +Turn the flower over and examine its inner face. Notice the large, +round, and usually upright petal at the back, the two smaller ones +on each side, and the boat-shaped body between them, formed of +two small petals more or less united at the apex. Press the side +petals gently down with the thumb and forefinger and notice how +the essential organs are forced out from the little boat in which +they are concealed. Observe how the end of the style is bent over +so as to bring the stigma uppermost when the petals are depressed. +Imagine the legs of a bee or a butterfly resting there as he probed +for honey; with what organ would his body first come in contact when +he alighted? If his thorax and abdomen had previously become dusted +with pollen when visiting another flower, where would the pollen be +deposited? Do you notice anything in the color, shape, or odor of +this flower that would be likely to attract insects? Have you ever +observed insects hovering around flowers of this kind; for example, +in clover and pea fields, and about locust trees and wistaria vines? +What kind of insects, chiefly, have you seen about them? + +[Illustration: FIGS. 318-322.—Dissection of a papilionaceous flower: +318, front view of a corolla; 319, the petals displayed: _v_, +vexillum, or standard; _w_, wings; _k_, keel; 320, side view with +all except one of the lower petals removed, showing the essential +organs protected in the keel: _l_, loose stamen; _st_, stamen tube; +321, side view, showing how the anthers protrude when the keel is +depressed; 322, ground plan. (_After_ GRAY.)] + +Remove the sepals and petals from one side, and sketch the flower in +longitudinal section, showing the position of the pistil and stamens. +Then remove all the petals, and spread in their natural order on the +table before you, and sketch as they lie (Fig. 319). Label the large, +round upper one, _standard_ or _vexillum_; the smaller pair on each +side, _wings_, and the two more or less coherent ones in which the +pistil and stamens are contained, _keel_. + +=239. The stamens.=—Count the stamens, and notice how they are united +into two sets of nine and one. Stamens united in this way, no matter +what the number in each set, are said to be _diadelphous_, that is, +in two brotherhoods. Notice the position of the lone brother, whether +below the pistil—next to the keel—or above, facing the _vexillum_. +Would the projection of the pistil, when the wings are depressed, be +facilitated to the same extent if the opening in the stamen tube were +on the other side, or if the filaments were _monadelphous_—all united +into one set? Flatten out the stamen tube, or sheath, formed by the +united filaments, and sketch it. + +=240. The pistil.=—Remove all the parts from around the pistil, and +sketch it as it stands upon the receptacle. Look through your lens +for the stigmatic surface (223). See if there are any hairs on the +style, and if so, whether they are on the front, the back, or all +around. Can you think of a use for these hairs? Notice how the long, +narrow ovary is attached to the receptacle; is it sessile, or raised +on a short footstalk? If the latter, label the footstalk, _stipe_. +Select a well-developed pistil from one of the lower flowers, open +the ovary parallel with its flattened sides, and sketch the two +halves as they appear under the lens. Notice to which side the ovules +are attached, the upper (toward the vexillum) or the lower, and label +it, placenta. How many locules has the ovary? How many carpels? How +can you tell (216)? + +=241. Plan of the flower.=—Diagram the flower in horizontal and +vertical section, and decide upon the following points:— + + Numerical plan + Symmetry + Regularity + Union of parts + Position of the ovary + +[Illustration: FIGS. 323, 324.—Salvia: 323, a newly opened flower, +showing the pollen-covered anther striking the back of a visiting +bee; 324, an older flower, with the protruding pistil rubbing against +the back of a bee covered with pollen from a younger flower.] + +=242. Significance of these distinctions.=—These distinctions are +important to remember, not only because they are very useful in +grouping and classifying plants, but because they mark successive +stages in the evolution of the flower. In general, flowers of a +primitive type and less advanced organization are characterized +by having their organs free and hypogynous, while the more highly +developed forms show a tendency to consolidation and union of parts, +and the epigynous mode of insertion. Irregularity also, since it +indicates specialization and adaptation to a particular purpose, may +be regarded as a mark of advanced evolution. + +[Illustration: FIGS. 325, 326.—Salvia: 325, longitudinal section +through a flower, showing the rocking connective which is struck at +_a_ by a visiting insect; 326, section of the same flower after being +visited, showing the lower arm of the connective pushed back and +lowering the anther.] + +=243. Dissection of a bilabiate flower.=—Make a similar study of the +flower of a salvia, dead nettle, catalpa, or other specimen of the +bilabiate kind. Make diagrams and report as to (1) numerical plan; +(2) presence or absence of parts; (3) regularity; (4) union of parts; +(5) position of ovary. Observe especially the relative position of +stigma and anthers; is it such that the pollen can reach the stigma +without external aid? Does the peculiar shape of the corolla serve +any other purpose than to attract the attention of insect visitors +by its conspicuous appearance? What is the use of the projecting +underlip? Is it any convenience to a bee, for instance, to have a +platform to rest on while gathering pollen or honey? What is the use +of the arched upper lip? Cut it away and notice the exposed condition +of the stamens and pistil. Turn a flower upside down; what would be +the effect on a visiting bee or butterfly? (Exps. 83, 84.) + +[Illustration: FIG. 327.—Staminodia, transformed stamens of canna +simulating petals: _pet_, petals; _st_, staminodia.] + +[Illustration: FIG. 328.—Flower of a cactus (_cereus greggii_), +showing transition from scales to petals.] + +=244. Morphology of the flower.=—We have seen that the venation of +petals and sepals corresponds in a general way with that of foliage +leaves of the class to which they belong, and that their arrangement +around their axis is analogous to the arrangement of foliage leaves +on the branch. In our study of inflorescence, it was observed that +flowers and flower buds occur in the same positions where leaf buds +occur, and that they are subject to the same laws of arrangement +and growth. We learned, also, in our study of leaves, something +about the wonderful modifications that these organs are capable of +undergoing; and finally, an examination of a number of different +flowers has shown them capable of undergoing modifications to an +equal or even greater extent, and examples of the transition of +almost any floral organ into another may be observed by one who will +take the trouble to look for it. Stamens and petals are found in all +stages of transformation, from the slightly flattened filament of +the star-of-Bethlehem, or the yellow pollen speck on the petal of +a rose, to the brilliant staminodia, or transformed stamens of the +canna (Fig. 327), which simulate petals so perfectly that their real +nature is never suspected by the ordinary observer. The transition +from spines and bracts to the brilliant corolla of the cactus (Fig. +328) is so gradual that we are hardly aware of it till we examine a +specimen and see it actually going on before our eyes. + +It must not be supposed, however, that an organ is ever developed as +one thing and then deliberately changed into something else. When we +speak loosely of one organ being modified into another, the meaning +is merely that it has developed into one thing instead of into +something else that it was equally capable of developing into. + +=245. The course of floral evolution.=—For the reasons mentioned, +the flower is regarded as merely a branch with modified leaves and +the internodes indefinitely shortened so as to bring the successive +cycles into close contact, the whole being greatly altered and +specialized to serve a particular purpose. With this conception +of the nature of the flower, we can readily see that the less +specialized its organs are and the more nearly they approach in +structure and arrangement to the condition of an undifferentiated +branch, the more primitive and undeveloped is the type to which it +belongs. On the other hand, if the parts are highly specialized and +widely differentiated from the crude branch, a proportionately high +stage of floral evolution is indicated. + + + V. FUNCTION AND WORK OF THE FLOWER + + MATERIAL.—For this exercise, flowers of the mallow + family—hollyhock, abutilon, mallow, hibiscus, cotton, okra, + etc.—are particularly recommended because they have pollen grains + so large that they can be studied fairly well with a hand lens. + Lily, tulip, iris, etc., will also meet all essential conditions of + the study outlined in the text. A strand of silk from a pollinated + ear of corn is an excellent example for showing the growth of the + pollen tube, under the microscope. + + APPLIANCES.—A compound microscope; a watch crystal; sugar solution + of 5 to 15 per cent. + + EXPERIMENT 77. TO SHOW THE GERMINATION OF POLLEN GRAINS.—Put a drop + of 5 per cent sugar solution into a watch crystal or a concave + slide, seal by smearing the edges with vaseline, and cover with a + glass to keep out the dust. Examine at intervals of five minutes + under the microscope (a hand lens will show the result with the + specimens recommended, though not so well), and the pollen grains + will be observed to send out long filaments or tubes into the + sirup, as a germinating seedling sends its radicle into the soil. + +=246. Office of the flower.=—The one object of the flower is the +production of fruit and seed, and all its wonderful specializations +and variations of form and color tend either directly or indirectly +to this end. + +=247. Pollination and fertilization.=—It was stated in 215 that only +in very exceptional cases can seed be developed unless some of the +pollen reaches the stigma. This act, called _pollination_, is an +essential step in seed production, but is not sufficient to secure +that end unless it leads to the process known as _fertilization_. +Successful pollination is a necessary preliminary to fertilization, +and the one begins where the other ends. + +=248. The next step toward fertilization.=—Examine with a lens the +pollinated pistil of a mallow, lily, or other large flower, and +notice the flabby, withered appearance of grains that have stood for +some time on the stigma, as compared with those of a newly opened +anther. Can you account for the difference? Touch the tip of your +tongue to the stigma, or apply the proper chemical test, and it will +be seen that the sticky fluid which it exudes, contains sugar. Refer +to Exp. 77 and say what effect this substance has on the pollen. + +[Illustration: FIG. 329.—A pollen grain emitting a tube (magnified).] + +=249. The pollen tube.=—The same thing happens when a pollen grain +falls on the moist surface of the stigma. It begins to germinate by +sending a little tube down into the substance of the pistil, and the +withered appearance of the grains on the stigma results from the +nourishment in them having been exhausted, just as the endosperm of +the seed is exhausted when the embryo begins to germinate. Here, +however, the analogy ends, for the pollen tube is not adapted, like +the radicle of the seedling, to absorb and convey nourishment up to +the other parts, but to feed and carry down to the ovary two small +bodies called _generative cells_, which it discharges there, and +then its work is done and it disappears. So it must be borne in mind +that when we speak of the germination of the pollen grains, we mean +something really very different from the germination of a seed. + +=250. The course of the pollen tube.=—Cut the thinnest possible +section through a freshly pollinated pistil and place under the +microscope. Watch the pollen tubes from the grains on the stigma as +they descend through the style toward the ovary. A pollinated strand +of corn silk—which is only a very much elongated style—is excellent +for this purpose. It is so thin and transparent that no section need +be made, and the tube can be traced as it works its way down through +the entire length of the threadlike style to the young grain, or +ovary, on the cob. The time required for the tube to penetrate to the +ovary varies in different flowers according to the distance traversed +and the rate of growth. In the crocus it takes from one to three +days; in the spotted calla, about five days; and in orchids, from ten +to thirty days. As a rule, it occupies only a few hours. Sometimes +the pistil is hollow, affording a free passage to the pollen tube; +in other cases, it is solid, and the growing tube eats its way down, +as it were, feeding on the substance of the pistil as it grows. How +is it in the flower you are examining? It takes a grain of pollen +to fertilize each ovule, and where more than one seed is produced +to a carpel, as is commonly the case, at least as many pollen +tubes must find their way to each locule of the ovary as there are +ovules—provided all are fertilized. + +[Illustration: FIG. 330.—Diagram of a simple flower, showing course +of the pollen tube: _a_, transverse section of an anther before its +dehiscence; _b_, an anther dehiscing longitudinally, with pollen; +_c_, filament; _d_, base of floral leaves; _e_, nectaries; _f_, wall +of carpels; _g_, style; _h_, stigma; _i_, germinating pollen grains; +_m_, a pollen tube which has reached and entered the micropyle of the +ovule; _n_, stalk of ovule; _o_, base of the inverted ovule; _p_, +outer integument or testa; _q_, inner integument; _t_, cavity of the +embryo sac; _u_, its basal portion; _z_, oösphere.] + +=251. Fertilization.=—When a pollen tube has penetrated to the ovary, +it next enters one of the ovules, usually through the micropyle +(Fig. 330, _m_). There it penetrates the wall of a baglike inclosure +called the _embryo sac_ (Fig. 330, _u_, _t_, _z_), where one of the +generative cells emitted by the pollen tube fuses with a large cell +contained in the embryo sac, known as the _germ cell_, or _egg cell_ +(Fig. 330, _z_). The fusion of these two bodies is what constitutes +fertilization. The cell formed by their union finally develops into +the embryo, and the other contents of the sac into the endosperm, and +the ripened ovules become seeds. + +=252. Stability of the process of fertilization.=—The phenomena +that characterize the functions of fertilization and reproduction +are the most uniform and stable of all the life processes, varying +little not only in different species and orders, but throughout the +whole vegetable kingdom. And since these functions furnish a more +reliable standard for judging of the real affinities of the different +groups than do mere external resemblances, which are more liable +to variation and may often be accidental, they have been chosen by +botanists as the ultimate basis for the classification of plants. + +=253. Embryology.=—The study of the developing plantlet, known as +_embryology_, is a comparatively recent branch of science, and has +greatly enlarged our knowledge of the life history of both plants and +animals, by bringing to light resemblances that exist between the +most widely divergent species in their earlier stages of development +and thus showing traces of a common origin. It has shown further, +that every individual plant or animal, in its development from the +embryo to the mature state, passes briefly through stages apparently +similar to those which the species has traversed in the course of +its evolution. This summary repetition, by the individual, of the +evolutionary progress of its kind is known as the _biogenetic law_, +and through its intelligent application some of the most intricate +problems in both physiology and psychology have been solved. + + + Practical Questions + + 1. Does the biogenetic law throw any light on the resemblances + sometimes observed between leaves of different ages in unlike + species; for example, the fig and the mulberry? (170; Field Work, + p. 195.) + + 2. Can you name any other examples of plants or parts of plants + which show mutual resemblances in their early stages that do not + exist at maturity? + + 3. Are there other causes than those acting under the biogenetic + law to which some of these resemblances may be referred; for + instance, the down and waxy coating on young leaves and bud scales? + (148, 207.) + + + VI. HYBRIDIZATION + + MATERIAL.—Several potted plants of tulip, lily, or any attainable + large flowered kind; or preferably a small plot in a garden or + nursery. + + APPLIANCES.—A pair of dissecting scissors, a camel’s-hair brush, + and some paper bags. + + EXPERIMENT 78. DOES IT MAKE ANY DIFFERENCE WHETHER A FLOWER HAS + ITS OVULES FERTILIZED WITH ITS OWN POLLEN OR WITH THAT OF ANOTHER + FLOWER OF THE SAME KIND?—Carefully remove the _unopened_ anthers + from a bud of a tulip, or other large flower just ready to unfold + (Fig. 331), inclose the mutilated bud in a small paper bag until + the stigma is mature, as shown by stickiness, then transfer to it + with a camel’s-hair brush some pollen from another flower. On the + stigma of a second flower of the same kind place some of its own + pollen, and cover with a paper bag until the stigma withers, to + keep foreign pollen from reaching it by means of wind or insects. + Watch until seeds are matured. Which flower produces the more + seeds or the better ones? Plant the seeds; which produce the more + vigorous progeny? + +[Illustration: FIGS. 331-333.—Flower of Lorillard tomato: 331, newly +opened bud, showing stage in which the stamens should be removed; +332, mature flower: _cx_, calyx; _c_, corolla; _s_, stamens; _st_, +stigma; 333, flower with stamens removed for pollination. (Natural +size.)] + + EXPERIMENT 79. CAN A FLOWER BE FERTILIZED WITH POLLEN OF A + DIFFERENT KIND?—Dust the stigma of a tulip or a lily, from which + the stamens have been removed, with pollen from a narcissus, iris, + or amaryllis. Cover to protect from wind and insects. Are any seeds + produced? + + Experiments of this kind, to be conclusive, ought to be performed + on a sufficient number of plants and through at least three + generations. This is hardly practicable for class work, but + students who are specially interested in the subject may carry + on experiments at home, or supply their place, to some extent, + by observations out of doors, if there are any farms or gardens + accessible. + +[Illustration: FIGS. 334-335.—Seeds of Bartlett pear, showing the +advantage of cross-fertilization: 334, cross-fertilized; 335, +self-fertilized.] + +=254. Self-fertilization= takes place when a stigma is pollinated +from the same flower. Horticulturists have long known that continued +self-fertilization, or “in-breeding” as it is called by nurserymen, +tends to deteriorate a stock; but Charles Darwin was the first to +explain, by a series of pains-taking experiments, the meaning of +those careful adjustments which the more highly organized plants, as +a rule, have developed to guard against it. + +[Illustration: FIG. 336.—Showing the effect of in-breeding on corn in +one generation. The two left-hand rows are from self-fertilized seed.] + +=255. Cross-fertilization= is effected by the pollination of a +stigma from another flower of the same variety or species. As +used by practical horticulturists, the expression means that the +two factors, pollen and ovule, belong to different plants. Since +pollination is the necessary antecedent to fertilization, and the +only means by which we can control it, the breeder’s part in crossing +is concerned with this act only and nature does the rest. Darwin’s +experiments—and they are confirmed by the experience of plant growers +everywhere—prove that the offspring from crossing different plants +of the same kind is usually stronger and more productive than that +from self-fertilized ones; and if the parent stocks are grown in +different places and under different conditions, the offspring +is more vigorous than that from the same kind of plants grown +under like conditions. For instance, plants from crossed seeds of +morning-glory vines growing near each other exceeded in height those +from self-fertilized seeds as 100:76; while the offspring of plants +growing under different conditions exceeded those of the other cross, +in height, as 100:78; in number of pods, as 100:57, and in weight +of pods, as 100:51. Knowledge of this kind, when applied to the +raising of fruits and grains for market, is of incalculable value to +gardeners and farmers, and also to the amateur who raises fruits or +flowers for pleasure. + +=256. Hybridization= is the crossing of two plants of different +species or of widely separated varieties of the same species. The +resulting offspring is a _hybrid_. Hybridization can take place only +within certain limits. If the species are too unlike, the pollen will +either not take effect at all, or the resulting offspring will be too +weak and spindling to live; or if they survive, will not be able to +set seed (Exp. 79). + +[Illustration: PLATE 11.—Hybrid between a red and a white carnation, +showing characters intermediate between the two parents.] + +=257. Effects of hybridization.=—The most important practical uses of +hybridizing are: (1) it “breaks the type” by causing plants to vary, +and thus gives the breeder a fresh starting point for a new strain; +and (2) when the parent species are not too unlike, it accentuates +the good effects of crossing, and sometimes gives rise to offspring +greatly surpassing either parent in size and vigor. In regard to +variability it may act in three ways: (1) the hybrid may wholly +resemble one parent or the other, in which case there is, of course, +no variation; (2) it may resemble one parent more than the other; or +(3) it may show a blending of the characters of the two, as when a +cross between a red poppy and a white gives rise to a light pink, or +a mixed red and white variety. In the first two cases, the characters +of the parent that manifest themselves are said to be _dominant_; +those which do not, _recessive_. + +[Illustration: FIG. 337.—Effect of hybridization between related +species in imparting superior vigor to offspring: _M_, Californian +black walnut (_Juglans californica_), male parent; _F_, Eastern black +walnut (_J. nigra_), female parent; _H_, hybrid.] + +=258. Mendel’s Law.=—So long ago as the middle of the last century +it was discovered by Gregor Mendel, an Austrian investigator, that +hybrids vary in certain cases according to a fixed law, by means +of which the proportionate share of the characteristics of the two +parent forms inherited by the offspring can be foretold with almost +mathematical precision. The controversy over Darwin’s “Origin of +Species,” which was raging at the time, caused Mendel’s discoveries +to be overlooked for a generation, and it is only within the last +few years that their importance has been realized. The principle +of variation demonstrated by him in a series of experiments, +and confirmed by later investigators is, briefly, this: If two +parents differing in some fixed characteristic be crossed, the +entire offspring, in the first generation, will be like the parent +possessing the dominant quality. If all the seed of this generation +is planted and carefully protected from foreign pollen, its offspring +composing the second generation from the parents will vary in the +proportion of ¾ dominants (_D_, _D′_, line 2 of the diagram) to ¼ +recessives (_R_). Planting _all_ the seeds of the second generation +and carefully shielding their progeny from foreign pollen, we +get from _D_, line 2, all pure dominants (_D_, line 3)—that is, +plants producing only their own type, and from _R_, line 2, all +pure recessives (_R_, line 3). But from each of the two sets of +dominants, _D′D′_, line 2, marked “impure” in the diagram, and so +called because their seeds may produce both dominants and recessives, +we get the same result as in the second generation, namely: pure +dominants (_D′D′_, line 3), pure recessives (_R′R′_, line 3), and +impure dominants (_D″D″_, _D″D″_, line 3). If it were possible to +distinguish the seeds of these impure dominants before germination +and plant them only, for no matter how many generations, the result +would always be approximately the same,—¼ pure dominants, ¼ pure +recessives, and ²⁄₄ impure dominants capable of producing both +dominants and recessives in the proportion of 3:1. + +[Illustration: Diagram illustrating Mendel’s Law.] + +=259. Practical applications.=—Four principles of great importance +to plant breeders follow from this law in cases to which it applies: +(1) the absence of variation in the first generation of hybrids is +no sign that it may not occur later; (2) pure recessives always +breed true; hence, if they show the desired character, no further +selection is necessary for that character; (3) pure dominants always +breed true, but the distinction between pure and impure is usually +not apparent in one generation; (4) the descendants of “impure” +parents cannot be depended upon to come true to either type, but +impure dominants may breed recessives, and _vice versa_, with the +presumption, however, of 3:1 in favor of dominants. + + + Practical Questions + + 1. Would hybridization account for some of the diversities + mentioned in 170? (See 257.) + + 2. To what cases would it not apply? (256; Exp. 79.) + + 3. Would it be worth while to try to hybridize the potato and + squash? The squash and pumpkin? The lily and rose? Sweetbrier and + wild rose? Apple and peach? Wild crab and sweet apple? Blackberry + and strawberry? Blackberry and raspberry? Lemon and watermelon? + Lemon and orange? Why, or why not, in each case? (256; Exps. 78, + 79.) + + + VII. PLANT BREEDING + + MATERIAL.—If practicable, visit a market garden, a florist’s + establishment, or, lacking these, the fruit and vegetable stalls of + a city market. + +=260. Fixing the type.=—It is the tendency of plants to vary under +the influence of climate, soil, food supply, crossing, and other +causes perhaps unknown to us, that makes the plant breeder’s art +possible. When a horticulturist sets out to produce a new fruit +or vegetable, he first forms in his mind a clear idea of what he +wants—whether increase of yield or size, resistance to cold, drought, +or disease, improvement in flavor, color, shape, etc., or change +in the time of maturing or flowering (early and late varieties). +Suppose, for instance, he wishes to produce an oxeye daisy with +all the disk florets changed to white ones like the rays. He will +begin by selecting plants with the greatest number of rays and the +most conspicuous ones that he can find, and sowing the seeds of +the flowers which show the greatest tendency to the development of +these qualities. He will continue this process from generation to +generation, rigorously destroying all specimens that do not approach +nearer the ideal sought, until all disposition to “rogue,” as the +tendency to revert is called, has been eliminated. When variations +cease to occur and the seed of the new variety always “come true,” +the type is said to be _fixed_; though some care will always be +necessary to keep it so, as the influence of changed surroundings and +the danger of mixture with foreign pollen must always be provided +against. + +[Illustration: FIG. 338.—A field of pumpkins grown from selected +seed.] + +=261. Survival of the fittest.=—In the fierce struggle continually +going on among both plants and animals for food, shelter, and elbow +room in the world, any individual that happens to vary in a way which +adapts it to its surroundings a little better than its rivals, has an +advantage that will enable it to survive when less favored members of +the species will perish. Its offspring, or some of them, may inherit +this quality and transmit it, with the attendant advantage, to their +posterity, and so on, till that particular breed outstrips all +competitors, and in time, as the less favored intervening forms die +out, becomes differentiated as a new species. This is, in brief, the +doctrine of natural selection and the survival of the fittest. + +=262. Artificial selection.=—Artificial selection enables the breeder +to accomplish more quickly what nature appears to do by the slow +process of natural selection. It is by this means that our choicest +fruits and vegetables have been developed from greatly inferior, and +sometimes inedible, wild forms. Plants respond so readily to the +influence of selection, and the changes brought about by it are so +rapid, that new styles of fruits and flowers succeed each other in +the market with almost as great frequency and in as ready response +to demand as the new styles of women’s bonnets and gowns in the shop +windows. + +[Illustration: FIG. 339.—Variation in blackberry leaves due to +hybridization.] + +=263. Causes of variation.=—While man cannot directly force plants +to vary in any given direction, he can hasten the process of +variation by crossing, or by changing the conditions under which +they are growing. This is called “breaking the type.” Hybridization +furnishes the readiest means to this end. Change of food supply, +especially if accompanied by excess of nourishment, is probably the +expedient that ranks next in effectiveness. Light, temperature, +moisture, character of the soil, exposure to wind, and the like, +also have their influence; and in adapting themselves to changes +in these various conditions, plants are apt to exhibit an unusual +number of variations, when removed from one locality to another, +especially if the difference in soil and climate is very marked. +Now comes the breeder’s opportunity. By taking advantage of such +variations as may occur either spontaneously, or as the result of +his efforts to break the type, he will generally find some that will +meet his requirements; and knowing the effect produced by different +conditions, he can, to a certain extent, influence the course of +variation in the direction desired, by subjecting his specimens to +the conditions that tend to produce it. If he wishes to develop a +dwarf variety, for instance, he will take notice that overcrowding, +lack of nourishment, and cold tend to produce that result in +nature, and by acting on this hint he can direct his efforts more +intelligently. He will learn, too, not to waste time in trying to +breed a plant contrary to its nature. He must not expect to gather +figs from thistles by any art of selection or skill in culture. By +attention to Mendel’s law, a still further saving of time and labor +may be effected. + +It is obvious, from what has been said, that a breeder’s chance of +finding what he wants will be greater in proportion to the number +of individual plants he has to choose from. For this reason, a +horticulturist sometimes uses thousands and hundreds of thousands of +specimens of a single kind in conducting his experiments. In this way +he compresses into a short space of time the advantage that nature +can gain only by spreading her random experiments over a long series +of years, or even centuries. + +[Illustration: FIG. 340.—Mutation in twin ears of corn, showing the +sudden variations that sometimes occur, by which a new type may be +provided without the labor of selection.] + +=264. Mutation and variation.=—There are at least two ways in which +changes in vegetable and animal forms are thought to occur: (1) +by the preservation and fixation through selection and heredity, +of slight differences that may appear from time to time, such +divergences being called “fluctuating variations”; (2) by the +appearance now and then, due to causes as yet unknown, of definite +and sudden changes creating a new form at a single, though perhaps +small, leap. When such a change is temporary and passes away with +the individual in which it first appeared, it is called a “sport,” +and leads to no important results; but when it is inherited by the +offspring, so that it is capable of giving rise to a new species, +it constitutes a “mutation.” The value of a mutation to breeders +in saving time and trouble is obvious. Professor Hugo de Vries, a +Dutch botanist, was the first to call attention to the importance of +mutation and its bearing upon the production of new species. + +=265. Factors in the evolution of species.=—Variation, heredity, and +selection are the three principal agents underlying all changes, +whether for the improvement or deterioration of living organisms. +The influence of external surroundings in keeping up a variation +once begun, or in starting new ones, is also a factor that cannot +be disregarded. It is for this reason that natural species are so +much more stable than those brought about by man. The former, being +evolved in response to natural conditions, are liable to change +only as alterations in their surroundings are brought about by the +slow operation of natural causes. But the types resulting from the +breeder’s art, produced as they often are in response to human +demands and in direct opposition to the requirements of natural +conditions, are in a sense purely artificial, and can be preserved +only by keeping up the artificial surroundings by which they were +developed. Hence, the importance of diligent cultivation and constant +care and tillage, without which the most carefully selected stocks +may quickly “run out” and degenerate into worthless forms. + + + Practical Questions + + 1. Which are the more pliable to the breeder’s art, annuals or + perennials? Why? (91, 93, 262, 263.) + + 2. What advantage is gained by using buds and grafts instead of + seedlings in making new varieties of fruit trees? (257, 259, 260.) + + 3. Would it be practicable to breed new varieties of slow-growing + forest trees, like oak, cypress, redwood, from seeds? Why or why + not? (93, 262, 263.) + + 4. Can you account for the existence of the numerous intermediate + forms between the different species of oaks found in nature? (255, + 257.) + + 5. If a breeder wished to produce a sweet-scented daisy or pansy, + how would he make his selections? (260.) + + 6. Which would be the more useful for his purpose, a plant that + showed a general tendency to variability, or one that remained + steadily fixed to its type? (260.) + + 7. What could he do to break the type? (263.) + + 8. Would an intelligent breeder set out to produce edible roots and + tubers from wheat or barley? (263.) + + 9. Would he think it worth while to try to develop a fleshy fruit + from a filbert or a walnut tree? From a haw? From sheepberry and + black haw? From tupelo (ogeechee lime)? (263.) + + 10. Suppose a florist should wish to change the color of a rose + from pink to deep red; how could he hasten the process? (257, 263.) + + 11. Explain why it is so much easier to produce new varieties of + plants when there are already many kinds in existence, as, for + example, the rose, peach, and chrysanthemum. (255, 256; Exps. 78, + 79.) + + + VIII. ECOLOGY OF THE FLOWER + + + A. THE PREVENTION OF SELF-POLLINATION + + MATERIAL.—Any kind of unisexual flowers obtainable. Some good + examples for illustrating points mentioned in the text are: for + spring and early summer, catkins of almost any of our common forest + trees,—oak, hickory, willow, poplar, etc.; tassels and young ears + of early corn; for summer and early fall, flowers of late corn, and + of melon, squash, pumpkin, or others of the gourd family. Examples + of _dichogamy_ are: evening primrose, showy primrose (_Œnothera + speciosa_), willow herb (_Epilobium_), dandelion, artichoke, + sunflower, or any of the composite family; of _dimorphism_: + English primrose (_Primula_), loosestrife (_Pulmonaria_), bluets + (_Houstonia_), partridge berry; _cleistogamic_: fringed polygala, + violets. Peanuts, while not technically classed as cleistogamic, + are strictly close-fertilized, and approach the type so nearly that + they may be used as an illustration. + +=266. Ecology= is the study of plants and animals in relation to +their surroundings. The principal modifications that flowers undergo +in this respect are in adapting themselves for (1) pollination, and +(2) protection. + +[Illustration: FIGS. 341, 342.—Unisexual flowers of willow: 341, +staminate; 342, pistillate.] + +[Illustration: FIG. 343.—Twig of oak with both kinds of flowers: +_f_, fertile flowers; _s_, _s_, staminate; _a_, pistillate flower, +enlarged; _b_, vertical section of pistillate flower, enlarged; _c_, +portion of one of the sterile aments, enlarged, showing the clusters +of stamens.] + +=267. Unisexual flowers.=—The advantages of cross fertilization were +shown in the last two sections. It was also shown that the first +step taken by the breeder to secure this result is to render the +flower incapable of self-fertilization, by removing the stamens. +Nature accomplishes the same purpose by the more effectual expedient +of providing imperfect, or _unisexual_ flowers, in which stamens +only, or pistils only, occur in the same flower. When the stamens +alone are present, the flower is said to be staminate, or _sterile_, +because it is incapable of producing seeds of its own, though its +pollen is a necessary factor in seed production. If, on the other +hand, the ovary is present and the stamens absent, the flower is +pistillate and _fertile_; that is, capable of producing fruit when +impregnated with pollen. Sometimes both stamens and pistils are +wanting, as in the showy corollas of the garden “snowball,” the +hydrangea, and the rays of the sunflower. Such blossoms are said to +be _neutral_, from the Latin word _neuter_, meaning neither, because +they have neither pistils nor stamens. They can, of course, have no +direct part in the production of fruit, but are for show merely. +(231.) + +=268. Monœcious and diœcious plants.=—When both kinds of flowers, +staminate and pistillate, are borne on the same plant, as in the oak, +pine, hickory, and most of our common forest trees, they are said +to be _monœcious_, a word which means “belonging to one household”; +when borne on separate plants, as in the willow, sassafras, and black +gum, they are _diœcious_, or “of two households.” Draw a flowering +twig of oak, pine, or willow. Where are the fertile flowers situated? +Notice how very much more numerous the staminate flowers are than the +fertile ones. Why is this necessary? (275.) + +[Illustration: FIGS. 344, 345.—Flower of fireweed (_Epilobium +angustifolium_): 344, with mature stamens and immature pistil; 345, +the same a few days older, with expanded pistil after the anthers +have shed their pollen. (_After_ GRAY.)] + +=269. Dichogamy= is the name applied to a condition where the stamens +and pistils mature at different times, as in the evening primrose, +oxeye daisy, and most of the composite family. It is a very common +method in nature for preventing self-pollination, and quite as +effective as the monœcious arrangement, since it renders the flowers +practically unisexual. + +[Illustration: FIGS. 346-347.—Flower of pulmonaria: 346, long styled; +347, short styled.] + +=270. Dimorphism= denotes a condition in which the stamens and +pistils are of different relative lengths in different flowers of +the same species, the stamens being long and the pistils short in +some, the pistils long and the stamens short in others. Flowers +of this sort are said to be _dimorphous_, or _dimorphic_, that +is, of two forms; and some species are even _trimorphic_, having +the two sets of organs long, short, and medium, respectively, in +different individuals. Examples of dimorphic flowers are the pretty +little bluets (_Houstonia cœrulea_), the partridge berry, the swamp +loosestrife, and the English cowslip. Of trimorphic flowers we have +examples in the wood sorrel and the spiked loosestrife (_Lythrum +salicaria_) of the gardens. These flowers were a great puzzle to +botanists until the celebrated naturalist, Charles Darwin, proved +by experiment that the seeds produced by pollinating a dimorphous +flower with its own pollen, or with pollen from a flower of similar +form, are of very inferior quality to those produced by impregnating +a long-styled flower with pollen from a short-styled one, and _vice +versa_. + +[Illustration: FIGS. 348-350.—Three forms of loosestrife (_Lythrum +salicaria_).] + +=271. “Nature abhors self-fertilization.”=—These are the +three principal methods by which nature provides against +self-fertilization. Other cases occur in which the relative position +of the two organs is such that self-pollination is difficult, or +impossible, as in the iris and bear’s grass; or the pollen may be +incapable of acting on the stigma of the flower that produced it. +This aversion to self-fertilization is so great that many flowers, +even when capable of it, will give preference to the pollen of +another plant of the same kind, if dusted with both. From his +observations on the behavior of plants in reference to this function, +Charles Darwin drew the conclusion that “Nature abhors perpetual +self-fertilization.” + +=272. Cleistogamic flowers.=—Apparent exceptions to this rule are +the hidden flowers found on certain plants which seem to have been +constructed with a special view to self-fertilization. They are +called _cleistogamic_, or closed, because they never open, but are +fertilized in the bud; and those of the fringed polygala do not +even rise above ground at all. Flowers of this kind can be found on +several species of violet, concealed under the leaves, close to the +ground; and the flowers of the peanut, found in the same situation, +while they open slightly, are close-fertilized and practically +cleistogamic. They are much more prolific than ordinary flowers, +but are not common, and seem to be a provision against accident, for +the plants producing them are generally provided with other flowers +of the usual kind,—some, as the violet, having elaborate special +adaptations for cross fertilization. + + + Practical Questions + + 1. Why does a strawberry bed sometimes fail to fruit well, although + it may flower abundantly? (267, 268.) + + 2. Are berries found on all sassafras trees? On all buckthorns? + Hollies? + + 3. Would a solitary hop-vine produce fruit? A solitary ash tree? + (267.) + + 4. Why is a mistletoe bough with berries on it so much harder to + find than one with foliage merely? (267, 268.) + + + B. WIND POLLINATION + + MATERIAL.—In spring, catkins of forest trees, staminate and + pistillate flowers of pine. At nearly all seasons, heads of grain + and panicles of various kinds of grass can be obtained. For + experiment, a potted plant of any kind, just about to bloom, may be + used. + + EXPERIMENT 80. TO TEST THE EFFECT OF SHUTTING OUT EXTERNAL + AGENCIES.—Tie paper bags over flower buds of different kinds when + nearly ready to open and leave until the flowers have withered. + On removing the bags, mark with colored threads the flowers that + had been covered, and watch until seed time. Do you notice any + difference in the number, size, or weight of the seed produced by + them and by those of the same kind left exposed? How do you account + for the difference, if there is any? By what agencies could foreign + pollen have been carried to the stigmas of the exposed flowers? If + any of the covered specimens wither and drop their seed vessels + without any attempt to fruit, examine a fresh flower, and see if it + is capable of self-pollination. + + As already explained, experiments of this kind, to be conclusive, + should be tried on as many specimens as possible. The greater the + number of species and individuals included, the better. Where it is + not practicable to carry on experiments by the class, pupils who + are interested can make them at home. + +=273. The problem of pollination.=—When a plant has provided against +self-pollination, its problem is only half solved, as it must now +depend upon the conveyance of pollen to the stigma by extraneous +means. + +[Illustration: FIG. 351.—Feathery stigmas of a grass adapted to wind +pollination.] + +=274. Adaptations to wind pollination.=—A very large number of +plants, among which are included nearly all our principal forest +trees, grains, and grasses of every kind, depend exclusively upon +the wind for the distribution of their pollen. This being the case, +it is, of course, an advantage to them to get rid of all unnecessary +appendages that might hinder a free play of the wind among their +flowers, and so they consist, as a rule, of essential organs only +(Figs. 341, 342). Such flowers are often distinguished, however, +especially among grasses and low herbs, by large, feathery stigmas +that are well adapted to catch and hold any stray pollen grains which +may be floating in the air. Place a stigma of oat or other grass +under the microscope and you will probably see a number of pollen +grains clinging to its branches. + +=275. The disadvantages of wind pollination.=—This is a very clumsy +and wasteful method, however, for so much pollen is lost by the +haphazard mode of distribution that the plant is forced to spend its +energies in producing a vast amount more than is actually needed, +and great masses of it are frequently seen in spring floating like +patches of sulphur on ponds and streams in the neighborhood of pine +thickets. Like those that are self-pollinated, wind-pollinated +flowers are generally very inconspicuous, devoid of odor, and of all +attractions of form or color, because they have no need of these +allurements to attract the visits of insects. Besides being wasteful, +wind pollination is very uncertain. The pollen cannot be blown about +very well unless it is dry, and in rainy weather it may all be rotted +or washed away before it can reach the stigmas that are ready to +receive it. + + + Practical Questions + + 1. Why do the flowers of oak, willow, and other wind-fertilized + plants generally appear before the leaves? (274.) + + 2. Can you account for the showers of “sulphur” sometimes reported + in the newspapers? (275.) + + 3. Do you see any connection between the feathery stigmas of most + grasses and their mode of pollination? (274.) + + 4. Why are house plants not apt to seed so well as those left in + the open? (Exp. 80.) + + 5. Why are the tassels of corn placed at the tip of the stalk? + (274.) + + 6. Can you trace any connection between the winds and the corn + crop? (274.) + + 7. If March winds should cease to blow, would vegetation be + affected in any way? (274.) + + 8. Why are wind-fertilized plants generally trees or tall herbs? + (274.) + + 9. Is it good husbandry to plant different varieties of corn or + other grain in the same field, if it is desired to keep the strain + pure? (255, 274.) + + 10. Is water a good pollen carrier? (275.) + + 11. What is the only class of plants it is likely to reach? + + 12. What is the only other agency, besides wind and water, by which + this office can be performed? + + + C. INSECT POLLINATION + + MATERIAL.—Half a dozen panes of glass, about 6 × 9; squares of + bright-colored cloth or paper; a few spoonfuls of honey or sirup; + perfumes of various kinds, preferably flower extracts; fetid and + disagreeable smelling substances, such as a bit of decaying animal + or vegetable matter. Observations on living plants can best be made + out of doors or in a greenhouse, as opportunity offers. + + EXPERIMENT 81. HAS THE COLOR OF FLOWERS ANY ATTRACTION FOR + INSECTS?—Place half a dozen panes of ordinary window glass out of + doors or in an open window to which insects can have free access. + Lay under the first pane a piece of black paper or cloth, and under + the others bright-colored pieces of red, blue, white, yellow, and + purple. Drop on the center of each pane a little honey or sirup, + and watch. Do insects show any color preferences? Which color + attracts fewest visitors? Which most? + + EXPERIMENT 82. DOES ODOR INFLUENCE INSECTS?—Try the same experiment + with different odors, removing the bright colors and sprinkling + some kind of perfume on each pane. Try also the effect of decaying + meat and other malodorous substances. Are any insects attracted + by these? What kinds? Does this account for the noisome smells + of the “carrion-flower” and skunk cabbage? What kinds of insects + are attracted by sweet-smelling substances? Do the greater number + appear to be attracted by these, or by foul odors? Are flowers of + the sweet-smelling or the foul-smelling kind more common in nature? + Do insects seem to be more strongly influenced by colors or by + odors? + +=276. The color of flowers=, being an adaptation to changing external +conditions, is a very unstable quality, and varies greatly within +the limits of the same species. Even on the same stem, flowers of +different colors are often found, due, probably, to hybridization. +Yet, notwithstanding all this apparently random intermingling of +hues, the range of color for each species is confined, approximately, +within certain limits. Nobody has ever seen a blue rose or a yellow +aster; and though the florist’s art is constantly narrowing the +application of this law, it still remains true that in a state of +nature, certain colors seem to be associated together in the floral +art gamut. Yellow is considered the simplest and most primitive color +in flowers, and blue the latest and most highly evolved. Yellow, +white, and purple, in the order named, are the commonest flower +colors in nature; blue, the rarest. Do you see any relation between +these facts and the color preferences of insects? + +=277. Advantages of insect pollination.=—It is evident that this is +a much more certain as well as a more economical method of securing +pollination than through the haphazard agency of wind or water. +In probing around for the nectar or the pollen upon which they +feed, these busy little creatures get themselves dusted with the +fertilizing powder, which they unconsciously convey from the stamen +of one flower to the pistil of another. Insects usually confine +themselves, as far as possible, to the same species during their +day’s work, and since less pollen is wasted in this way than would +be done by the wind, it is clearly to the advantage of a plant to +attract such visitors, even at the expense of a little honey, or of a +liberal toll out of the pollen they distribute. + +=278. Special partnerships.=—Some plants have adapted themselves +to the visits of one particular kind of insect so completely that +they would die out if that species were to become extinct. The +well-known alliance between red clover and the bumblebee was brought +to light when the plant was first introduced into Australia. It grew +luxuriantly and blossomed profusely, but would never set seed till +the bumblebee was introduced to keep it company. + +[Illustration: FIG. 352.—Pod of _yucca_ pierced by the _Pronuba +yuccasella_.] + +[Illustration: FIG. 353.—Pronuba pollinating pistil of yucca.] + +[Illustration: FIG. 354.—Moth resting on yucca blossom.] + +A remarkable partnership of this kind exists between the _pronuba_, +or yucca moth, and the flowering yuccas, of which the bear’s grass +and Spanish bayonet are familiar examples. The pods of these plants +are never perfect, but all show a constriction at or near the middle, +such as is sometimes seen in the sides of wormy plums and pears. This +is caused by the larvæ of the moth, which feed upon the unripe seeds. +A glance under the nodding perianth of a yucca blossom (Fig. 354) +will show that the short stamens are curved back from the pistil in +such a manner that, under ordinary circumstances, the pollen cannot +reach the stigma except by the rarest accident. But the yucca moth, +as soon as she has deposited her eggs in the seed vessel, takes care +to provide a crop of food for her offspring by gathering a ball of +pollen in her antennæ and deliberately plastering it over the stigma +(Fig. 353). In this way fertilization of the ovules and maturing of +the fruit is secured. The larvæ feed on the unripe seeds for a time, +but so few are destroyed in proportion to the number matured that the +plant can well afford to pay the small toll charged in return for the +service rendered. + +[Illustration: FIG. 355.—Upper boughs of a caprifig tree, showing an +abundant crop of spring fruit.] + +[Illustration: FIG. 356.—Female wasps issuing from the galls of +caprifigs, in which the eggs are laid.] + +=279. Caprification of the fig.=—A more complicated case of +specialization is that of the Smyrna fig of commerce—the only one +of the species that is capable of perfecting seeds. The staminate +flowers are borne on a separate tree, the caprifig, which grows wild +in the countries bordering on the Mediterranean. The caprifigs, +as the fruit of this tree is called, are worthless except as the +breeding and nesting places of a small insect, the fig wasp. This +insect is the necessary agent in conveying pollen from the stamens of +the caprifig to the pistils of the Smyrna fig, which it penetrates at +certain seasons of the year in the effort to lay its eggs. In order +to insure _caprification_, as this process is called, the caprifigs +are strung by hand on fillets of cord or raffia and hung about on the +trees which are to be fertilized. In this case we have an example +of a threefold partnership between man, the fig tree, and the wasp, +which is necessary to the existence of two of the parties. + + + D. PROTECTIVE ADAPTATION + + EXPERIMENT 83. ARE THE FLORAL ENVELOPES OF ANY USE?—Carefully + remove the calyx and corolla from a young flower bud on a growing + plant and see what will happen. Remove them from a flower just + unfolding. Mark each by tying a colored thread lightly around the + petiole and see if it sets as many seeds, or as good ones, as the + unmutilated flowers on the same plant. + + EXPERIMENT 84. IS THE POSITION OF A FLOWER ON THE STEM OF ANY + IMPORTANCE?—Invert a blossom of pea or sage, and see what parts + would come in contact with the body of a visiting insect. How would + its chances for pollination be affected? Try to make a flower grow + in an inverted position by tying or weighting it down, and watch + the effect on seed production. + + EXPERIMENT 85. IS THE POSITION OF FLOWERS ON THE STEM INFLUENCED + BY LIGHT?—Place a potted plant with expanding flower buds near a + window so that the light will reach it from one side only, and + notice the position of the buds. After a day or two reverse the + position with regard to light, and watch whether any change of + position takes place. + +[Illustration: FIGS. 357-359.—Flower of monkshood, showing the +changes by which it returns to its original position under the +influence of geotropism after the axis of inflorescence, s, has +been inverted: 357, inverted position; 358, change due to negative +geotropism; 359, change due to lateral geotropism.] + + EXPERIMENT 86. IS THE POSITION OF FLOWERS ON THE STEM INFLUENCED + BY GEOTROPISM?—Lay a potted plant of lily of the valley, larkspur, + gladiolus, or digitalis in a horizontal position, tie the main stem + to keep it from changing its direction of growth, and leave for two + or three days in a place where it is lighted equally on all sides. + How do the individual flowers behave? What part bends to turn them + up? Vary the experiment by turning the pot bottom upwards so + that the flowering axis will point downwards. This can be done by + inclosing the pot in a bag of strong cheesecloth, with the string + tied loosely but firmly around the foot of the stem to prevent the + contents from falling out, and suspending the whole bottom upwards. + In making these experiments, use flowers that grow in a long + cluster, or raceme, and hold the main axis in a vertical position + by tying or weighting it down. Watch the behavior of the individual + flowers. Arrange another pot containing the same kind of plant, in + the same way, and suspend one in a dark place, keeping the other + in the light. Does the same movement take place in both? Is it in + response to light, or to gravity? + +[Illustration: FIGS. 360, 361.—Protection of pollen in the thistle: +360, position at night, or during wet weather; 361, position in +sunshine.] + +[Illustration: FIGS. 362, 363.—A bell flower: 362, position in +daylight; 363, position at night, or during wet weather.] + +=280. Means of protection.=—Where plants have adapted themselves to +insect pollination, it is, of course, important to shut out intruders +that would not make good carriers. In general, small, creeping +things, like ants and plant lice, are not such efficient pollen +bearers as winged insects, and hence the various devices, such as +hairs, scales, and constrictions, at the throat of the corolla, by +means of which their access to the pollen is prohibited. To this +class of adaptations belong the hairy filaments of the spiderwort, +the sticky ring about the peduncles of the catchfly, the swollen +lips of the snapdragon, the scales or hairs in the throat of the +hound’s-tongue, the velvet petals of the partridge berry, and the +recurved edges of corollas like those of the morning-glory and +tobacco, over which small crawling insects cannot easily climb. + +Of flowers that are pollinated by night moths, some close during +the day, as the four-o’clock and the evening primrose; and _vice +versa_, the morning-glory, dandelion, and dayflower (_Commelyna_) +unfold their beauties only in the sunlight. For similar reasons, +night-blooming flowers are generally white or very light-colored, and +shed their fragrance only after sunset. A nodding position is assumed +by many flowers at night, or during a shower, to keep the pollen from +being injured by dew or rain. + +[Illustration: FIG. 364.—A flower of the trumpet vine (_Tecoma +radicans_) adapted to pollination by humming birds and humming bird +moths, which has been pierced by a bee or bird for honey.] + +[Illustration: FIG. 365.—Head of the swordbill, a bird adapted to +feeding on nectar from long, tubular corollas.] + +=281. Insect depredators.=—The secretion of honey is a common +means of attracting insects, and various adaptations, such as +spurs, sacs, and pockets, are provided for protecting it against +unwelcome intruders. In general, plants that have long, tubular +flowers, like the trumpet honeysuckle (_Lonicera sempervirens_) and +the trumpet vine, are reserving their sweets for humming birds, or +long-tongued moths and butterflies. This protective device is not +always successful, however, against insect depredators, for it is not +uncommon to find such corollas with a puncture near the base, made by +wasps or bees, and sometimes by humming birds themselves, in their +impatience to get at the feast before the flower is open. Through the +breach thus made, a rabble of petty thieves can then find entrance. + + + Practical Questions + + 1. Of what use is the brilliant coloring of the camellia? The large + flowers of the magnolia? The perfume of the rose and the violet? + The fetid odor of the ailanthus? (277; Exps. 81, 82.) + + 2. Are the tastes of insects in regard to odors always the same as + ours? (Exp. 82.) + + 3. Have flowers any economic value except for decorative purposes? + + 4. Can you name any that are used as food or beverages? Any that + furnish spices and flavorings? Drugs, medicines, or dyes? + + 5. What commercial food product is obtained almost entirely from + flowers? + + 6. Name some of the flowers that are most valued by the beekeeper. + + 7. Mention another important industry that is entirely dependent on + flowers. + + 8. Name some of the flowers that are most important to the perfumer. + + 9. Why do the seeds of fruit trees so seldom produce offspring true + to the stock? (256, 257, 271, 277.) + + 10. Would you place a beehive near a field of buckwheat? Of clover? + Near a strawberry bed? In a peach orchard? Near a fig tree? Under a + grape arbor? + + 11. Why are very conspicuous flowers, like the camellia, hollyhock, + and pelargoniums, so frequently without odor? + + 12. Why is the wallflower “sweetest by night”? (280.) + + 13. What advantage can flowers like the morning-glory gain by their + early closing? (280.) + + 14. Of what use to the cotton plant, Japan honeysuckle, and + hibiscus is the change of color their blossoms undergo a few hours + after opening? (277, 278, 280.) + + 15. Why does the Japan honeysuckle, which has run wild so + abundantly in many parts of our country, produce so few berries? + (278, 280.) + + 16. If the trumpet vine grows in your neighborhood, examine a + number of corollas and account for the dead ants found in them. + Account also for the large hole (sometimes three quarters of an + inch in diameter) often found near the base of the tube. (281.) + + 17. Do you see any connection between the greater freshness and + beauty of flowers early in the morning, and the activity of bees, + birds, and butterflies at that time? + + 18. The flowers most frequented by humming birds are the trumpet + honeysuckle, cardinal flower, trumpet vine, horsemint (_Monarda_), + wild columbine, canna, fuchsia, etc.; what inference would you draw + from this as to their color preferences? + + + Field Work + + 1. The ecology of the flower is so suggestive a subject and so + peculiarly appropriate to outdoor work that it seems hardly + necessary to point out the many attractive fields of inquiry it + opens to the student of nature. In this way alone can experiments + in insect pollination be carried on to the best advantage. Try + the effect of enveloping buds of various kinds in gauze so as + to exclude the visits of insects, and note the result as to the + production of fruit and seed. Envelop a cluster of milkweed + blossoms in this way and notice how much longer the flowers so + protected continue in bloom than do the others; why is this? Try + the same experiment upon the blooms of cotton and hibiscus, if you + live where they grow, and see whether the characteristic change in + color occurs in flowers from which insects have been excluded, and + whether good seed pods are produced by them. Try the effect upon + fruit production of excluding insects from clusters of apple, pear, + and peach blossoms. + + 2. Make a list of all the outdoor plants, both wild and cultivated, + that are found blooming in your neighborhood, keeping a record of + the earliest specimens of each as you find them. The best way is to + keep a sort of daily calendar, and at the end of each month give a + summary of the species found in bloom during that period. In this + way a fairly complete annual record of the flowering time of the + different plants for that vicinity will be obtained. The record + should be kept up the whole year round. Don’t stop in winter, + but go straight on through the coldest as well as the hottest + season, and you will make some surprising discoveries, especially + if the record is continued year after year. Give the common name + of each plant, adding the botanical one if you know it. Any facts + that you may know or may discover in regard to particular plants, + such as their medicinal or other uses, their poisonous or edible + properties, the insects that visit them, and in the case of weeds, + their origin and introduction, will greatly enhance the interest + and value of the record. + + + + +CHAPTER VIII. FRUITS + + + I. HORTICULTURAL AND BOTANICAL FRUITS + + MATERIAL.—Green ears of corn or wheat, fresh pods of beans, young + fruits of apple, grape, tomato, melon, buckeye, chestnut, or pecan. + A young fruiting stem of squash, gourd, or tomato. + + APPLIANCES.—Coloring fluid, glasses of water, a piece of cardboard, + tin-foil, vaseline. + + EXPERIMENT 87. WHERE DO THE FOOD SUBSTANCES CONTAINED IN FRUITS + COME FROM?—Apply your food tests to the pulp of a young apple, + squash, bean pod, chestnut, buckeye, or a “green” ear of corn or + wheat, and see what it contains. Test the stem and roots of a plant + of the same kind in the same way. Do you find the same foods in + them? Where is the food stored? + + EXPERIMENT 88. THROUGH WHAT PARTS OF THE STEM AND FRUIT DO WATER + AND NOURISHMENT TRAVEL TO THE SEED?—Cut a young squash or cucumber + from the vine, leaving stem enough to insert by its cut end in a + glass of eosin solution. Leave for two or three days, then make a + vertical section through the stem and fruit. What course has the + liquid followed? Can you trace some of it into each seed? Do you + see now a use for the seed stalk and the rhaphe? + + EXPERIMENT 89. DOES THE SURFACE OF FRUITS GIVE OFF WATER BY + TRANSPIRATION?—Try Exp. 59, using in place of leaves a young + squash, eggplant, or a bunch of grapes, and after a day or two + notice whether any moisture has been given off. If the fruit skin + gives off moisture, it is natural to expect that it would be + provided with stomata, like other transpiring organs. To find out + whether this is so, place a thin piece of the outer epidermis of + a grape, tomato, plum, or apple under the microscope. Do you find + stomata on any of them? Do you see anything else? Try the skin of + an apple, and compare the corky dots you find there with those on + the bark of a young dicotyl stem (118) and decide what they are. + + EXPERIMENT 90. WILL FRUITS RIPEN WELL IN THE ABSENCE OF LIGHT AND + AIR?—Envelop a number of immature fruits in bags of dark cloth or + paper so that no light can reach them. Keep a number of others well + coated with oil or vaseline, and watch. Do the fruits so treated + mature as quickly or develop as fully as those of the same kind + left untreated? + +[Illustration: PLATE 12.—The improvement of fruits by cultivation and +selection: 1, the common wild gooseberry; 2, Houghton gooseberry, +seedling of the wild form; 3, Downing gooseberry, seedling of the +Houghton. (All natural size, adapted from Bailey.)] + + EXPERIMENT 91. WHAT IS THE USE OF THE RIND TO THE FRUIT?—Select + two apples of equal size, peel one, and weigh both. After 12 to 24 + hours, weigh them again. Which shows the greater loss in weight? + Leave peeled and unpeeled fruits in an exposed place and see which + is the more readily attacked by insects. Which decays the sooner? + What are some of the uses of the rind? + +=282. What is a fruit?=—Horticulturally and commercially the +distinction between a fruit and a vegetable depends very much upon +the use we make of it—whether as food, or as a mere gratification of +the palate. Broadly speaking, those fruits that are lacking in sugar, +as the tomato and cucumber, are classed as vegetables. Botanically, a +fruit is any ripened seed vessel, or ovary, with such connected parts +as may have become incorporated with it; and hence, to the botanist, +a boll of cotton, a tickseed, or a cocklebur is just as much a fruit +as a peach or a watermelon. + +=283. Classification of fruits.=—For convenience of description, +fruits are classed as: + +(_a_) Dry or fleshy, according as they have a more or less hard and +bony, or soft and fleshy, texture. + +(_b_) Dehiscent, or indehiscent, according as they open at maturity +in a regular way to discharge their seed, or remain closed until the +covering wears away or is burst by the germinating embryo. + +Fleshy fruits are very seldom dehiscent, though some few, as the +balsam apple and the chayote, or one-seeded squash, discharge their +seed when mature. The banana and some other fleshy fruits, when +peeled, separate along regular lines, and in this respect behave very +much as if they were fleshy pods. + +=284. When is a fruit ripe?=—A fruit is ripe horticulturally, when +it is good to eat; it is ripe botanically, when it has set its seed. +Many of our choicest table fruits, such as the pineapple, banana, and +most varieties of fig, seldom are botanically ripe, since they rarely +produce perfect seeds. + +It is the constant effort of the horticulturist to develop those +parts of a plant that are useful to man, while in a state of nature +the plant seeks to develop such parts as best serve its own purpose +in the struggle for existence. The plants most useful to man have, +as a general thing, been subjected to a long course of artificial +breeding and selection. They are forced developments, often +monstrosities, from the plant’s point of view, if we could conceive +of it as capable of having an opinion. Nature is continually striving +to reclaim them; and if left to themselves, they must either obey +“the call of the wild,” or die out. + +[Illustration: FIG. 366.—A seedless citrange, hybrid between the +orange and the lemon.] + +=285. Seedless fruits and vegetables.=—As the seed is the most +important thing to the plant, the edible parts in wild fruits are, as +a rule, subsidiary to its development. In a state of nature, fruits +will generally wither and drop from the stem, if for any reason they +have become incapable of perfecting their seed. It is only in a few +kinds, limited to those which can successfully propagate themselves +by other means, that the production of seed does not take place. +Among cultivated species, however, where propagation is carefully +provided for by man, the seed is of less importance, and sterile +varieties that might soon die out under natural conditions, continue +their existence indefinitely under his fostering hand. The seeds +of edible fruits are, as a general thing, both indigestible and +unpalatable (21), and hence the efforts of the horticulturist are +directed largely to getting rid of them, or to very greatly reducing +their size and number in proportion to the edible parts. + +=286. How seedless fruits arise.=—The perfecting of seed requires a +great consumption of food and energy on the part of the plant, and +when it is led, for any reason, to expend an unusual amount of force +in some other function,—as for instance, in producing tubers or in +growing bulbs,—it is apt to bear few seeds and to depend more or less +completely upon other methods of reproduction. + +Among cultivated plants, selection on the part of man, whether +conscious or unconscious, has perhaps contributed more than any +other cause to bring about the same result. To this agency is +probably due the development of our common domestic fig, of which +over four hundred varieties that mature fruits without fertilization +are cultivated in the United States alone. The fig was one of the +earliest fruits known to cultivation; and the early navigators, +ignorant of the processes of fertilization, would naturally, in +choosing specimens to carry home with them, select only fruit-bearing +trees. Such of these as matured fruits would be preserved and +propagated, until, by repeated selection, hundreds of edible +varieties have been developed that ripen fruits without caprification +(279). + +=287. The use of the fruit to the plant.=—The object of the fruit is +to furnish protection to the seeds during their period of development +and inactivity, and to aid in various ways the work of dispersal. +It probably takes part also in digesting and diffusing nourishment +for the use of the developing seeds. It has been shown in previous +chapters that plants, almost without exception, are in the habit of +storing up food in various ways as a provision for fruiting. That a +large portion of the stored nourishment is used up in the performance +of this function is proved by its disappearance from those parts—for +example, from fleshy roots, such as beets and turnips, after they +have “gone to seed.” + + + Practical Questions + + 1. What is the use of the down on the peach? The bloom of the plum + and grape? [202, (1); Exp. 91.] + + 2. Why are apples, pears, plums, and other fleshy fruits nearly + always rosier on one side than on the other? (Exp. 90.) + + 3. Can annuals be improved in any other way than by seed selection? + + 4. Would a seedless annual be perpetuated under natural conditions? + + 5. Why is decrease of moisture and increase of light desirable as + the fruiting season approaches? (126, 127; Exp. 90.) + + 6. Why are turnips, carrots, and other fleshy roots unfit to eat if + left over till the plants have seeded? (92, 287.) + + + II. FLESHY FRUITS + + MATERIAL.—A specimen of each of the four principal kinds of fleshy + fruits. Examples of the pome are: apple, pear, quince, rose hip, + haw; of the berry: grape, tomato, cranberry, currant, gooseberry, + lemon; of the pepo: melon, squash, pumpkin; of the drupe: peach, + plum, cherry, dogwood. Specimens of the commoner kinds can nearly + always be found in the market; if nothing better is available, + pickled and dried ones may be used—figs, prunes, dates, raisins, + etc. + +[Illustration: FIG. 367.—Outside of an apple, showing lenticels on +the skin.] + +=288. Dissection of a pome fruit.=—Examine with a lens the outside of +an apple or a pear. Can you make out the lenticels? What difference +in color do you notice between the ripe and unripe fruit? What +difference in taste? What substance would you judge from this, do +ripe fruits contain which green ones do not? Test both kinds for +sugar and starch; which contains the more of each? Strictly speaking, +sugar and starch are merely different forms of the same chemical +compound. In ripe fruits the starch has been cooked by the sun and +converted into sugar. + +With the point of a pencil separate the little dry scales that cover +the depression in the center of the fruit at the end opposite the +stem. How many of them are there? How does this accord with the +plan of the flower as outlined in 229? They are the remains of the +sepals, as will be more apparent on comparing them with the larger +and more leaflike ones on a hip, which is clearly only the end of the +footstalk enlarged and hollowed out with the calyx sepals at the +top. Cut a cross section midway between the stem and the blossom end, +and make an enlarged sketch of it. Label the thin, papery walls that +inclose the seed, _carpels_. How many of them are there, and how many +seeds does each contain? The carpels, together with all that portion +of the fruit which surrounds and adheres to the ovary, constitute +the _pericarp_, or wall of the seed vessel. The fleshy part of the +apple is no part of the ovary proper, but consists merely of the +receptacle, or end of the footstalk, which becomes greatly enlarged +and thickened in fruit. Look for a ring of dots outside the carpels, +connected (usually) by a faint scalloped line. How many of these dots +are there? How do they compare in number with the carpels? With the +remnants of the sepals adhering to the blossom end of the fruit? + +[Illustration: FIG. 368.—Cross section of a pome: _pl_, placenta; +_c_, carpels; _f_, fibrovascular bundles.] + +[Illustration: FIG. 369.—Vertical section of a pome: _p_, peduncle; +_f_, fibrovascular bundles; _s_, seeds; _pl_, placenta; _c_, carpel.] + +Next make a vertical section through a fruit, and sketch, enlarging +it sufficiently to show all the parts distinctly. Observe the line of +woody fibers outside the carpels, inclosing the core of the apple. +Compare this with your cross section; to what does it correspond? +Where do these threads originate? Where do they end? Can you make +out what they are? (176.) Notice how and where the stem is attached +to the fruit. Label the external portion of the stem, _peduncle_; +the upper part, from which the fibrovascular bundles branch, the +_receptacle_. It is the enlargement of this which forms the fleshy +part of the fruit. Try to find out, with the aid of your lens and +dissecting pins, the exact spot at which the seeds are attached to +the carpels, and label this point, _placenta_. Notice whether it is +in the axis where the carpels all meet at their inner edges, or on +the outer side. Observe, also, whether the seed is attached to the +placenta by its big or its little end. If you can find a tiny thread +that attaches the seed to the carpel; label it, seed stalk. Fruits +of this kind are classed, botanically, as _pomes_. Write, from your +analysis, a definition of the pome. + +[Illustration: FIGS. 370, 371.—Enlarged receptacle of Carolina +allspice (_Calycanthus_), containing fruits attached to its inner +surface: 370, exterior; 371, vertical section.] + +=289. Modifications of the receptacle.=—Compare with the drawings +you have made, a haw and a hip. What points of agreement do you see? +What differences? Which of the two more closely resembles the typical +pome? The receptacle is subject to a variety of modifications, +and forms a part of many fruits, for example, the fig, lotus, and +calycanthus (Figs. 370, 371); but a fruit is not a pome unless the +containing receptacle becomes more or less soft and edible. + +=290. The pepo, or melon.=—Next examine a gourd, cucumber, squash, or +any kind of melon, and compare its blossom end with that of the apple +or pear. Do you find any remains of a calyx, or other part of the +flower? Examine the peduncle and observe how the fruit is attached +to it. Can you tell what made the outer epidermis of the rind? Put +a small piece under the microscope; do you see any stomata, or +lenticels? Cut cross and vertical sections, and sketch them, labeling +each part. There may be some difficulty in making out the carpels, +for they are not separate and distinct as in the pome, but confluent +with the enlarged receptacle, which in these fruits forms the outer +portion of the rind, and also with each other at their edges, so +as to form one unbroken circle, as if they had all grown together. +And this is precisely what has happened. The placentas are greatly +enlarged and modified, and it may be necessary to refer to the +diagram, Fig. 372, _c_, in order to make them out. How many locules, +or chambers, are there in your specimen? How many placentas? Notice +that these are central and double, but extend to the pericarp before +dividing so that they appear to be parietal, and twice their real +number, which is only three. Are the seeds vertical, as in the apple, +or horizontal? Look for the little stalk, or thread, that attaches +them to the placenta. + +_Pepo_ is the name given by botanists to this kind of fruit. Write in +your notebook a proper definition of it, from the specimens examined. + +[Illustration: FIG. 372.—Cross section of gourd: _c_, one of the +carpels in diagram. (_After_ GRAY.)] + +[Illustration: FIGS. 373, 374.—A potato berry: 373, exterior; 374, +cross section.] + +=291. The berry.=—Examine a tomato, an eggplant, a grape, cranberry, +lemon, or orange, in both cross and vertical section, and compare +it with the melon and the apple. What differences and resemblances +do you find? Cut a cross section, and draw, showing the attachment +of the seeds. How many locules are there? Normally the tomato is a +two-celled fruit, like the potato berry (Fig. 374), but it has been +so modified by cultivation that the original plan is not always easy +to distinguish. See if you can make it out. Do the seeds in your +specimen appear to be healthy and well developed, or are some of them +small and aborted? How do you account for this? (285, 286.) What +difference do you notice in color between the ripe and unripe fruit? +Write a definition of the berry from the study you have made of it. + +Berries are the commonest of all fleshy fruits, and the most variable +and difficult to define. In general, any soft, pulpy, or juicy mass, +like the grape and tomato, whether one or many seeded, inclosed in +a containing envelope, whether skin or rind, is a berry. Its typical +forms are such fruits as the grape, mistletoe, pokeberry, etc., +though such diverse forms as the eggplant, persimmon, red pepper, +orange, banana, and pomegranate have been classed as berries; and, in +fact, the melon and the pumpkin are only greatly modified kinds of +the same fruit. In popular language, any small, round, edible fruit +is called a berry. This is a good commercial classification, though +not botanically correct. + +[Illustration: FIG. 375.—Vertical section of a drupe. (_After_ GRAY.)] + +=292. The drupe, or stone fruit.=—Examine a section of a green plum, +peach, or cherry, before the stone has hardened, and tell from what +part it is formed. This stony covering, composed of the inner layer +of the pericarp, and enveloping the seed like an outer coat, is the +main distinction between the drupe and the berry, but it is not +always possible to make out its real nature except by an examination +of the young ovary. In a green drupe, before the stone has hardened, +its connection with the fleshy part is very evident, and the ripe +fruit will answer inquiries if we know how to put them. Open the +stone, and the seed will be exposed with its own coverings inside. +When a stone has more than one kernel,—for instance, an almond or +peach stone, —the stone is not a seed coat, but the hardened inner +wall of a seed vessel or ovary; for a seed coat can never contain +more than one seed, any more than the same skin can contain more than +one animal. + +All the fruits considered in this section belong to the fleshy class. +These form the bulk of the fruits sold in the market, and are of +special importance to the horticulturist. + + + Practical Questions + + 1. Is the tomato horticulturally a fruit or a vegetable? the + squash? eggplant? cranberry? olive? elderberry? pepper? date? + maypop? crab apple? black haw? To what class does each belong? + (283, 288-292.) + + 2. Of what use to the plant is the hard stone of the drupe? (21.) + + 3. Is the pulp of fleshy fruits agreeable to the taste before they + are ripe? After? What advantage is this to the plant? (21.) + + 4. Are the seeds of edible fruits, as a general thing, digestible + or agreeable to the palate? + + 5. Is this an advantage to man? To the plant? (21, 284, 285.) + + 6. What are the most common fleshy fruits in autumn? + + 7. With what vegetative parts of the plant does the skin of many + fruits present correspondences? Are these such as to indicate + homology, or analogy only, between them? (100, 118, 288, 289; Exp. + 89.) + + 8. Name six of the most watery fruits that grow in your + neighborhood. + + 9. Under what conditions as to soil, heat, moisture, etc., does + each thrive best? + + 10. Would a gardener act wisely to infer that because a fruit + contains a great deal of water it should be planted in a very wet + place? + + 11. Which contains more water, the fruit or the leaves of the apple? + + 12. Why does not the fruit, when separated from the tree, wither as + quickly as do the leaves? (Exp. 91.) + + + III. DRY FRUITS + + MATERIAL.—Some easily attainable specimens of dry fruits are (1) + nuts: acorn, hickory nut, walnut, chestnut, pecan, filbert; (2) + pods: pea and bean pods, capsules of larkspur, milkweed, jimson + weed, cotton; (3) grains: corn, wheat, oats, rice; (4) akene: + sunflower, thistle, dandelion, buckwheat, clematis. + +=293. Importance of dry fruits.=—Dry fruits are not in general so +conspicuous or so attractive as fleshy ones, but on account of their +great number and variety they offer a wide field for study. They are +also of great interest from an economic point of view: (1) because +they include the cereal grains that furnish so large a portion of our +food, and (2) because the greater part of the troublesome weeds that +infest our crops are scattered by fruits of this class. + +=294. Indehiscent fruits.=—These kinds are so simple that it will not +be necessary to give much time to them. Compare an acorn, a chestnut, +or a filbert with a ripe bean pod or with a capsule of morning-glory. +Try to open each with your fingers; which _dehisces_, or opens, the +more readily? Which is indehiscent, having no regular way of opening? +How many seeds or kernels do you find in the dehiscent pod? How many +in the indehiscent one? Would it be of any advantage for a one-seeded +pod to open? Remove the kernel from the indehiscent fruit; has it any +covering besides the shell? Which is the pericarp, and which the seed +coat? + +[Illustration: FIGS. 376, 377.—Nut of the pecan tree: 376, exterior; +377, cross section.] + +[Illustration: FIGS. 378, 379.—Nutlike seeds: 378, horse-chestnut; +379, seed of the fetid sterculia.] + +=295. The nut= is easily recognized by its hard, bony covering, +containing usually, when mature, a single large seed that fills +the interior. Care should be taken not to confound with true nuts, +large bony seeds, like those of the buckeye, horse-chestnut, date, +and the Brazil nut sold in the markets. In the true nut, the hard +covering is the seed vessel, or pericarp, and not a part of the seed +itself, though it often adheres to it so closely as to seem so. In +bony seeds, like those of the horse-chestnut and persimmon, the hard +covering is the outer seed coat. The distinction is not always easy +to make out unless the seed can be examined while still attached to +the placenta of the fruit. + +[Illustration: FIGS. 380, 381.—Akenes (magnified): 380, of buckwheat; +381, of cinque-foil.] + +[Illustration: FIGS. 382-384.—Cremocarps, fruits of the parsley +family.] + +=296. The akene=, of which we have examples in the tailed fruit of +the clematis, the tiny pits on the strawberry, and the so-called +seeds of the thistle, dandelion, and sunflower, is a small, dry, +one-seeded, indehiscent fruit, so like a naked seed that it is +generally taken for one by persons not acquainted with botany. It +is the commonest of all fruits, and there are so many kinds that +special names have been applied to some of the most marked varieties. +The akene of the composite family may generally be known by the +various appendages in the form of scales, hooks, hairs, or chaff, +that crown it (Figs. 309-314). The fruits of the parsley family are +merely a sort of double akene attached by the inner face to a slender +stalk from which it separates at maturity. + +The _samara_, or key fruit, is an akene provided with a wing to +aid in its dispersion by the wind. The maple, ash, and elm furnish +familiar examples. + +[Illustration: FIGS. 385, 386.—Samaras: 385, ailanthus; 386, maple.] + +[Illustration: FIGS. 387, 388.—Grain of wheat with husks on: 387, +front view; 388, back view.] + +=297. The grain=, so familiar to us in all kinds of grasses, is +economically the most important of all fruits. It is popularly +classed as a seed, and for practical purposes may be treated as such, +but it is really a modification of the akene in which the seed coats +have so completely fused with the pericarp that they can no longer be +distinguished as separate organs. Peel the husk from a grain of corn +that has been soaked for twenty-four hours, and you will find the +contents exposed without any covering; remove the shell of an acorn +or a hickory nut, and the seed will still be enveloped by its own +coats. Would it be of any advantage for the seed of an indehiscent +fruit, like a grain of corn or oats, to have a separate special +covering of its own? + +[Illustration: FIG. 389.—Follicle of milkweed.] + +[Illustration: FIG. 390.—Leaflike follicle of Japan varnish tree: +_S_, outer (dorsal) suture; _S′_, inner (ventral) suture.] + +=298. Dehiscent fruits.=—_Pod_, or _capsule_, is the general name +applied to all dehiscent fruits. The simplest possible kind of pod +is the _follicle_, composed of a single carpel, like those of the +larkspur, milkweed, and marsh marigold, and may be regarded as a +modified leaf. Examine one of these pods and you will find that +it splits down one side, which corresponds to the edges of the +leaf brought together and turned inward to form a placenta for the +attachment of the seed. This line of union is called a “suture,” from +a Latin word meaning a “seam.” + +=299. The legume.=—Get a pod of any kind of bean or pea, and observe +that it differs from the follicle in having two sutures or lines +of dehiscence. One of these runs along the back of the carpel and +corresponds to the midrib of the leaf; the other, corresponding to +the united edges of the carpellary leaf, always turns inward, toward +the axis of the flower, and forms the placenta. + +[Illustration: FIGS. 391-393.—Legumes: 391, legume of bean: _v_, +ventral suture; _d_, dorsal suture; 392, constricted legume of senna +(_Cassia Nelsonia_); 393, legume of a pea, with partially constricted +pod.] + +[Illustration: FIG. 394.—Loment of beggar-ticks.] + +The beggar-ticks, so unpleasantly familiar to most of us, are merely +a kind of legume constricted between the seeds and breaking up into +separate joints at maturity. What kind of indehiscent fruits do the +joints become when separated? (296.) + +[Illustration: FIG. 395.—Cross section of one-celled syncarpous +capsule of frostweed, with parietal placentæ. (_After_ GRAY.) FIG. +396.—Follicles of larkspur borne on the same torus, but distinct.] + +=300. Compound or syncarpous pods.=—The carpellary leaves may unite +either by their open edges, as if a whorl like that represented in +Fig. 188 were to grow together by the margins (Fig. 395); or each +may first roll itself into a simple follicle like the larkspur +and columbine (Fig. 396), and then a number of these may unite by +their ventral sutures into a single syncarpous capsule, with as +many locules as there are carpels (Fig. 398). The seed-bearing +sutures being all brought together in the center, the placenta +becomes _central_ and _axial_. In the first case (Fig. 395) the open +carpels form a one-chambered capsule, though the placentas sometimes +project, as in the cotton, so far as to produce the effect of true +partitions with a central axial placenta. In capsules with only one +compartment, the number of carpels can generally be determined by the +number of sutures or of placentas. + +[Illustration: FIG. 397.—Pods of Echeveria, contiguous, but distinct.] + +[Illustration: FIG. 398.—Capsule of Colchicum, with carpels united into +a syncarpous pod.] + +[Illustration: FIG. 399.—Capsule of corn cockle, with free central +placenta.] + + + Practical Questions + + 1. To what class of fruits does each of the following belong—rice; + beggar-ticks; poppy; peanut; jimson weed; chinquapin; caraway? + + 2. Is the coconut, as usually sold in the market, a fruit or a seed? + + Suggestion: carefully examine the “eyes,” from without and from + within; if you can get a specimen with the husk on, it will help to + a decision. + + 3. Can you name any syncarpous, or compound capsule, that is + single-seeded? + + 4. Can you name any indehiscent fruit that has normally more than + one seed? + + 5. Give a reason for the difference. (23.) + + 6. Name the weeds of your neighborhood that are most troublesome on + account of their adhesive fruits. + + 7. Do these fruits belong, as a rule, to the dehiscent or to the + indehiscent class? + + 8. Give a reason for the difference, if any is noted. (23.) + + + IV. ACCESSORY, AGGREGATE, AND MULTIPLE FRUITS + + MATERIAL.—For autumn and winter, examples of accessory fruits are: + pineapple, common apple, pear, rose hip; aggregate: magnolia, + tulip tree, wild cucumber, sweet flag (_Calamus_); multiple: osage + orange, sweet gum balls, pine cones, figs, fresh or dried. + + For spring and summer, examples of accessory fruits are: raspberry, + strawberry, squash, cucumber; aggregate: strawberry, blackberry, + Jack-in-the-pulpit; multiple: fig, mulberry. Most of those named + will be found to belong to more than one class; the strawberry, for + instance, is both accessory and aggregate; the fig and pineapple, + accessory and multiple. + +=301.= Besides the varieties already named, all fruits, whether +fleshy or dry, may be simple, accessory, aggregate, or collective. +Fruits of the first kind need no explanation; they consist merely +of a single ripened ovary, whether of one or more carpels, as the +peach, cherry, bean, and lemon. + +[Illustration: FIGS. 400, 401.—Vertical sections showing the relation +between a strawberry flower and fruit: 400, the flower; 401, the +fruit developed from it. The corresponding parts are indicated by +connecting lines; _r_, receptacle; _a_, sepal; _b_, petal; _s_, +stamens; _c_, carpel (akene in fruit); _p_, style of the pistil; +_pl_, pulp of the fruit.] + +=302. Accessory fruits= are so called because some other part than +the seed vessel, or ovary proper, is coherent with, or accessory to +it, in forming the fruit, as in the apple and the hip. The accessory +part may consist of any organ, but is more frequently the calyx or +the receptacle. In the strawberry, the little hard bodies, usually +called seeds, that dot the surface are the true fruits (akenes). A +vertical section through the center will show the edible part to +consist wholly of the enlarged receptacle. In the pineapple, the +edible stalk may be traced through a mass of flowers whose seed +vessels have become enlarged and ripened into fruits. + +=303. Aggregate fruits.=—Some accessory fruits, the strawberry and +blackberry for example, are, at the same time, aggregate; that is, +they are composed of a number of separate individual fruits produced +from a single flower. The cone of the magnolia and of the tulip tree +are aggregate fruits; can you name any others? + +[Illustration: FIGS. 402-404.—Multiple fruit of the pineapple: 402, +external view of a ripe fruit, showing the prolonged receptacle +growing into a new plant above, and the scaly bracted covering below; +403, vertical section through the axis of a fruit, showing _a_, the +receptacle, with _b_, _b_, the fleshy ovaries cohering around it +and forming the edible part of fruit; 404, a single “eye” or scale, +somewhat reduced, showing the scaly bract from the axil of which the +(generally) abortive flower originates.] + +=304. Collective, or multiple, fruits.=—The pineapple is an example +of both an accessory and a multiple fruit, being composed of the +ripened ovaries of a number of separate flowers that have become +more or less coherent. The osage orange, sweet gum balls, fig, and +mulberry are other examples of this class. + +=305. Dissection of a multiple fruit.=—Get one of the dried figs sold +by the grocers. Look at the small end where the skin originates; of +what part is it a modification? (289.) Can think of a reason for this +curious, urnlike enlargement of the receptacle? Is there anything +about the fig, for instance, that renders it peculiarly liable to be +preyed upon by birds and insects? Could any but a very small insect +get through the eye without injuring the fruit? Could it free itself +from the sticky mass inside and get out again without difficulty? +Would you judge from this that the caprification of the fig is easily +effected (279), even when the fig wasp is present? Can you now +account for the fact that over four hundred varieties of cultivated +figs ripen their fruit without fertilization? + +[Illustration: FIG. 405.—Vertical section of a fig, showing the +minute flowers inside the closed receptacle.] + +Open your specimen and examine the contents; what do you find? From a +dried specimen it will hardly be practicable to make out clearly that +the pulp of the fig consists of hundreds of tiny pistillate blossoms +that line the inner face of the receptacle. The little grains +usually taken for seeds are really small akenes—the ripened ovaries +of flowers that have been pollinated from the caprifig (279, 286). +Crush one gently and examine with a lens, or under a low power of the +microscope. It is these “botanically” ripe fruits (284) that give to +the dried figs of commerce their plumpness and their pleasant, nutty +flavor. Why are our native American figs lacking in these qualities +(279)? Could this defect be remedied? Do you know of any efforts +being made in that direction by American cultivators? + +[Illustration: FIGS. 406-409.—Non caprificated and caprificated +figs: 406, outside appearance of non caprificated fig; 407, outside +appearance of caprificated fig; 408, interior of caprificated fig; +409, interior of non caprificated fig.] + +=306. Fruit clusters.=—Be careful not to confound aggregate and +collective fruits with mere clusters, like a bunch of grapes or of +sumac berries. The distinction is not always easy to make out. The +clump of akenes that make up a dandelion ball, for instance, though +held on a common receptacle, like the mulberry and other collective +fruits, have so little connection with each other, and separate +so completely at maturity, as to partake more of the nature of a +cluster than of a collective fruit. The same is true of the clump +of tailed akenes that make up the fruit of the clematis. Though the +product of a single flower and thus technically an aggregate fruit, +they are really only a compact head or cluster. Some degree of +cohesion is necessary to constitute a cluster of matured ovaries into +an aggregate or a multiple fruit. + +=307. The individual fruits= that make up the various kinds just +described may belong to any of the classes mentioned in the two +preceding sections: those of the blackberry, for instance, are +drupes; of the strawberry, akenes; of the sweet gum, capsules. + + + Practical Questions + + 1. To what class of fruits would you refer the following: a banana; + a tickseed; a dewberry; a cocklebur; a string bean; a watermelon; + a cantaloupe; a pomegranate; a black haw; a dogwood berry; a red + pepper? + + 2. Tell which of the following are aggregate or multiple fruits, + and which are fruit clusters: an ear of corn; of wheat; a + buttonwood or a sycamore ball; a hop; a dewberry; a pine cone; a + prickly pear. (303, 304, 306.) + + 3. Tell the nature of the individual fruits composing the different + combinations mentioned in the last question. + + 4. Can you suggest any advantage that might accrue to a species + from having its fruits clustered or compound? (21, 23, 24, 287.) + + + Field Work + + 1. Study the various edible fruits of your neighborhood with regard + to their means of dissemination and protection. Consider the object + of the protective adaptations in each case, whether against heat, + cold, moisture, animals, etc. Notice the color of the different + kinds, and trace its significance; for example, the bright red of + the holly, the dull color of muscadine, black haw, and wild smilax. + Account for the prevalence of red among autumn fruits. Notice the + position of the fruit on the bough and explain its object; as, for + instance, the clustering of dogwood at the end of the twig, the + pendent position of grapes and honey locusts. Observe the relation + between the color and size of fruits and their grouping. What + advantage is it for sumac and bird haws to be gathered in large + clusters? + + 2. Compare wild with cultivated fruits and notice in what respects + man has altered the latter for his own benefit. Note, for instance, + the difference between cultivated apples and the wild crab, between + the cultivated grains and wild grasses. Observe the great number of + varieties of each kind in cultivation and try to account for it. + + 3. Notice the situations in which different kinds of fruits + grow, whether hot, dry, moist, windy, or sheltered, and how they + are affected by their surroundings. For example, account for + the difference between blackberries growing on a dry hillside, + and those in moist land along the borders of a stream. Give the + conclusions drawn from your observations in each case. + + 4. Notice what animals feed upon the different kinds, and whether + their visits are harmful or beneficial. Consider in what respects + the interests of the plant itself, the interests of man, and the + interests of other animals may clash or coincide. Examine the + vegetation along the hedgerows and borders of fields and old + fences. Notice the kind of plants that compose it—sumac, sassafras, + cedars, cat brier, etc. The list will be slightly different + for different localities, but this will not alter the general + conclusion. What kinds of fruits and seeds do these shrubs produce? + What kinds of living creatures frequent hedgerows and feed upon the + seeds of such plants? Do you see any relation between these facts + and one of the modes of seed dispersal? + + 5. Classify all the fruits you have collected during your + walk, under their proper heads, as fleshy or dry, dehiscent or + indehiscent, simple, accessory, aggregate, collective. Be careful + to distinguish between compact clusters, like the heads of clematis + or buttonwood, and truly compound fruits. + + + + +CHAPTER IX. THE RESPONSE OF THE PLANT TO ITS SURROUNDINGS + + + I. ECOLOGICAL FACTORS + + MATERIAL.—A number of small flowerpots filled with soils of as many + different kinds as can be found in the neighborhood. + +=308. Definition.=—By _ecology_ is meant the relation of plants to +their surroundings, which may be considered under three general +heads: their relations to inanimate nature, to other plants, and +to animals. The subject has been touched upon repeatedly in the +foregoing pages, and, in fact, it is impossible to treat of any +branch of botany without some reference to it. All that was said +about the adjustment of leaves for light and moisture, and their +adaptations for protection and food storage, about the devices for +pollination, and for fruit and seed dispersal, really belong to +ecology. + +=309. Symbiosis.=—The relations of plants to animate nature are +_biological factors_, and may act in two ways: (1) through the +destruction of vegetation by hungry animals and by parasitic and +disease-producing organisms; and (2) by associations for mutual +benefit, such as are described in section viii of chapter VII. +Associations of this kind are included under the general term +_symbiosis_, a word which means “living together.” In its broadest +sense symbiosis refers to any sort of dependence or intimate organic +relation between different kinds of individuals, and so may include +the climbing and parasitic habits; but it is usually restricted to +cases where the relation is one of mutual benefit. It may exist +either between plants of one kind with those of another, between +animals with animals, or between plants and animals, as in the case +of the clover and bumblebee, and the yucca and pronuba. + +[Illustration: PLATE 13.—Showing the quick response of vegetation to +surroundings. The upper cut shows the appearance of an irrigation +canal in the arid plains region, when first completed; the lower cut, +ten years after completion.] + +The occurrence of root tubercles on certain of the leguminosæ (63) is +a clear case of symbiosis, the microscopic organisms in the tubercles +getting their food from the plant and at the same time enabling it to +get food for itself from the air in a way that it could not otherwise +do. + +=310. Relations with inanimate nature.=—But it is to the relations of +plants with inanimate nature, and their grouping into societies under +the influence of such conditions, that the term “ecology” is more +strictly applied. The external conditions that lead to the grouping +are called _ecological factors_. The most important of these are +temperature, moisture, soil, light, and air, including the direction +and character of the prevailing winds. Each of these factors is +complicated with the others and with conditions of its own in a way +that often makes it difficult to determine just what effect any one +of them may have in the formation of a given plant society. + +=311. Temperature= may be even and steady, like that of most oceanic +regions, or it may be subject to sudden caprices and variations, +like the “heated terms” and “cold snaps” that afflict our Eastern +coast region every few years. It is not the average temperature of +a climate, but its extremes, especially of cold, that limit the +character of vegetation. + +Temperature probably has more influence than any other factor upon +the distribution of plants over the globe; but it can have little +or no effect in evolving local differences in vegetation, because +the temperature of any given locality, except on the sides of high +mountains, will ordinarily be the same within a circuit of many miles. + +=312. Moisture=, again, may be of all degrees, from the +superabundance of lakes and rivers and standing swamps, to the arid +dryness of the desert, and the water may be still and sluggish, +or in rapid motion. It may exist more or less permanently in the +atmosphere, as in moist climates like those of England and Ireland, +where vegetation is characterized by great verdure; or it may come +irregularly in the form of sudden floods, or at fixed intervals, +causing an alternation of wet and dry seasons. Moreover, the moisture +of the soil or the atmosphere may be impregnated with minerals or +gases, which may affect the vegetation independently of the actual +amount of water absorbed. + +[Illustration: FIG. 410.—The effect of cold—a Mt. Katahdin bog. +(_From_ Mo. Botanical Garden Rep’t.)] + +Snow is a form of water which may act in two entirely opposite ways: +(1) by keeping the atmospheric precipitation locked up in a solid +state and thus bringing about a condition analogous to drought—for +example, in arctic deserts and Alpine snow fields; (2) by causing +annual floods and overflows when it melts in the spring, as in the +Nile and Mississippi valleys. + +In cold temperate regions it also influences vegetation to a +considerable extent by covering the warm earth like a blanket during +winter, and thus protecting tender seeds and shoots that otherwise +would not be able to survive. + +[Illustration: FIG. 411.—Dogwood, a tree tolerant of shade, growing +and blooming in a deeply wooded glen.] + +=313. Light= may be of all degrees of intensity, from the blazing +sun of the treeless plain to the darkness of caves and cellars where +no green thing can exist. Between these extremes are numberless +intermediate stages: the dark ravines on the northern side of +mountains, the dense shade of beech and hemlock forests, and the +light, lacy shadows of the pines,—each characterized by its peculiar +form of vegetation. Absence of light, too, is usually accompanied by +a lowering of temperature and a reduction of transpiration, factors +which tend to accentuate the difference between sun plants and shade +plants, giving to the latter some of the characteristics of aquatic +vegetation. Generally, the tissues of these are thin and delicate, +and having no need to guard against excessive transpiration, they +wither rapidly when cut or exposed to too great intensity of heat and +light. + +[Illustration: FIG. 412.—A red cedar grown in a barren, wind-beaten +situation.] + +[Illustration: FIG. 413.—A red cedar grown under normal conditions.] + +=314. Winds= affect vegetation, not only as to the manner of +seed distribution and the conveyance of pollen, but directly by +increasing transpiration, and necessitating the development of strong +holdfasts in plants growing upon mountain sides and in other exposed +situations. The nature of the region from which they blow—whether +moist, dry, hot, cold, etc.—is also an important factor. In a +district open to sea breezes, live oaks, which require a salt +atmosphere, may sometimes be found as far as a hundred miles from the +coast. + +=315. Soil.=—While water is the most important, soil is perhaps the +most interesting of these factors to the farmer, because it is the +one that he has it most largely in his power to modify. It is to be +viewed under two aspects: first, as to its mechanical properties, +whether soft, hard, compact, porous, light, heavy, etc.; secondly, as +to its chemical composition and the amount of plant food-materials +contained in it. The first can be regulated by tillage and drainage, +the second by a proper use of fertilizers. + + EXPERIMENT 92. TO SHOW THE INFLUENCE OF SOIL AS AN ECOLOGICAL + FACTOR.—Fill a number of small earthen pots with all the different + kinds of soil that are to be found in your neighborhood. Keep well + moistened and make a list of the plants that appear spontaneously + in each. Is there any difference in the kinds produced by different + soils? In vigor or abundance of the same or different kinds? Do + more seedlings appear in any of the pots than could live if left + alone? What becomes of a majority of the seedlings that come up in + a state of nature? + + After a time, stop watering until all the plants are dead and new + ones cease to appear. Notice the rate at which vegetation dies out + in each and the kind of plants that can live longest without water. + Which of the different soils is capable of sustaining vegetation + longest without a fresh supply of moisture? To what quality of the + soil is this due? (Exp. 53.) + + + Practical Questions + + 1. Is the relation between man and the plants cultivated by him a + symbiosis? (309.) + + 2. Why is it that plants of the same, or closely related species + are found in such different localities as the shores of Lake + Superior, the top of Mt. Washington, and the Black Mountains in + North Carolina? (311, 330.) + + 3. Which of the five ecological factors mentioned in paragraphs + 311-315 has probably most largely influenced their distribution? + + 4. What is the prevailing character of the soil in your + neighborhood? + + 5. Is your climate moist or dry? Warm or cold? + + 6. Can you trace any connection between these factors and the + prevailing types of vegetation? + + + II. PLANT ASSOCIATIONS + + MATERIAL.—The subject is not well suited to laboratory work, + though, if time permits, it is recommended that a detailed study + be made of at least one typical hydrophyte, halophyte, and + xerophyte plant. Some good examples are: (1) Hydrophyte: pond + weed, waterlily, pipewort (_Eriocaulon_), bladderwort, arrowhead + (_Sagittaria_); (2) Halophyte: sea lavender, sea rocket, sea + lettuce, water hyacinth; (3) Xerophyte: cactus, century plant, + pineapple, stonecrop, purslane, lichen. + +=316. Modes of grouping.=—Plants group themselves in their favorite +habitats, not according to their botanical relationships, but with +regard to the predominance of one or more of the ecological factors +that influence their growth. Sometimes one or two species will +take practical possession of large areas, like the coarse grasses +that spread over certain salt marshes, or the pines that formerly +constituted the sole forest growth over extensive regions in North +Carolina and Maine. Exclusive growths of this kind over limited +areas are sometimes called plant _colonies_, and the individuals +composing them belong, as a general thing, to the hardy, pushing sort +known as “pioneers,” which are among the first to take possession +of new soil and force their way into unoccupied territory. But more +usually we find a great diversity of forms brought together by their +common requirements as to shade, soil, moisture, and other external +conditions. + +Any well-defined assemblage of plants, whether of one kind or many, +originating in such a common response to the same influences, is +called a _formation_. These associations are variously classed, +according to the nature of their habitat, as salt water, fresh water, +sand hill, swamp, bog, river bottom, or such other kinds as their +ecological character may indicate. Local conditions in limited +areas may lead to the segregation of smaller and more compact groups +called _societies_. This term, however, is used rather loosely, being +treated in some works as synonymous with formations, in others as +analogous with what have here been defined as colonies. + +[Illustration: FIG. 414.—A colony of Alabama primroses (_Œnothera +speciosa_).] + +=317. Principles of subdivision.=—The mixed associations described in +the last paragraph are quite independent of botanical relationships, +and any of the factors named in 310, or others of a different kind, +could be made the basis of their classification. They might be +grouped, for instance, according to their economic uses, or according +to origin, whether native or introduced, as best suited the purpose +of the classification in each case. The moisture factor, however, has +been generally agreed upon as the one most convenient for ordinary +purposes. Upon this principle plants are divided into three great +groups:— + +=Hydrophytes=, or water plants, those that require abundant moisture. + +=Xerophytes=, or drought plants, those that have adapted themselves +to desert or arid conditions. + +[Illustration: FIG. 415.—A water plant (_Limnophila_), with water +leaves and air leaves and transitional forms.] + +=Mesophytes=, plants that live in conditions intermediate between +excessive drought and excessive moisture. To this class belong +most of our ordinary cultivated plants and the greater part of the +vegetation of the globe. + +=Halophytes=, “salt plants,” is a term used to designate a fourth +class, based not directly upon the water factor, but upon the +presence of a particular mineral in the water or the soil which +they can tolerate. They seem to bear a sort of double relation to +hydrophytes on the one hand and to zerophytes on the other. + +=318. Hydrophyte societies.=—These embrace a number of forms, from +those inhabiting swamps and wet moors, to the submerged vegetation of +lakes and rivers. An examination of almost any kind of water plant +will show some of the physiological effects of unlimited moisture. +Take a piece of pondweed, or other immersed plant, out of the water +and notice how completely it collapses. This is because, being buoyed +up by the water, it has no need to spend its energies in developing +woody tissue. Floating and swimming plants will generally be found +to have no root system or very small ones, because they absorb their +nourishment through all parts of the epidermis directly from the +medium in which they live. That they may absorb readily, the tissues +are apt to be soft and succulent and the walls of the cells composing +them very thin. In some of the pipeworts (_Eriocaulon_), the ells +are so large as to be easily seen with the unaided eye. If you can +obtain one of these, examine it with a lens and notice how very thin +the walls are. Water plants also contain numerous air cavities, and +often develop bladders and floats, as in the common bladderwort and +many seaweeds. The leaves of submerged plants are usually either +greatly reduced in size or very much cut and divided, while the ones +that rise above water, like those of the water lily, are apt to be +large and entire, to facilitate floating, and have stomata on their +upper surface. Floating plants sometimes form such large colonies as +to be a serious menace to navigation. Well-known instances of this +are the water hyacinths in the St. John’s River, Florida, and the +vast formations of swimming gulfweed from which the Sargasso Sea +takes its name. + +[Illustration: FIG. 416.—Seaweed (_sargassum_) with bladderlike +floats.] + +[Illustration: FIG. 417.—A pioneer swamp colony of cattails. (_From_ +a photograph by Harry B. Shaw, U.S. Dept. Agr.)] + +=319. Swamp societies.=—These include what may be regarded as the +amphibious portion of the hydrophyte group. They compose the sedge +and cattail bogs, reed jungles, moss and fern thickets, forests of +cypress, magnolia, black gum, pine, tamarack, balsam, and the like. +The sedges and cattails are the pioneers of these societies, which +tend constantly to encroach upon the water and so prepare the way +for the advance of other colonists. Drawing their nourishment from +the loose soil in which they are anchored, and lacking the support +of a liquid medium, they develop roots and vascular stems. The roots +of plants growing in swamps have difficulty in obtaining proper +aëration on account of the water, which shuts off the air from them; +hence they are furnished with large air cavities, and the bases +of the stems are often greatly enlarged, as in the Ogeechee lime +(_Nyssa capitata_) and cypress, to give room for the formation of air +passages. The peculiar hollow projections known as “cypress knees” +are arrangements for aërating the roots of these trees. + +[Illustration: FIG. 418.—A Southern cypress swamp, showing on the +left the peculiar enlargements for aëration, known as “cypress +knees.” (_From_ Mo. Botanical Garden Rep’t.)] + +=320. Xerophyte societies= are adapted to conditions the reverse of +those affected by hydrophytes. The extreme of these conditions is +presented by regions of perennial drought, like our Western arid +plains and the great deserts of the interior of Asia and Africa. +Under these conditions plants have two problems to solve,—to collect +all the moisture they can and to keep it as long as they can. Hence, +plants of such regions have a diminished evaporating surface, owing +to the absence of foliage and the compacting of their tissues into +the stem, after the manner of the cactus and prickly euphorbia; or +their leaves may become thick and fleshy so as to resist evaporation +and retain large amounts of moisture, as in the case of the yucca and +century plant. They also frequently develop a thick, hard epidermis, +or cover themselves with protective hairs and scales. + +The principal types of xerophyte plants are: (1) the lichens, mosses, +and saxifrages found on bald rocks and mountain cliffs; (2) sand +plants, such as cockspur grass, sand spurry, wiregrass, and the +like, inhabiting sea beaches and pine barrens; (3) the sage brush, +greasewood, and switch plants of our Western alkali plains; (4) the +cactus and yuccas of southern California, Arizona, and Mexico; (5) +the acacias, agaves, and hardy “chapparal” thickets of southern +Texas and Mexico. The first class are of importance as the pioneers +and pathfinders of the xerophyte community. In tropical and polar +deserts alike they are the first settlers, and by aiding in the +disintegration of rocks and their gradual conversion into soil, they +pave the way for the coming of the higher plants, and it may be of +man himself. + +[Illustration: PLATE 14.—A xerophyte formation of yuccas, cacti, +and switch plants, near Zacatecas, Mexico. (_From_ a photograph by +Professor F. E. Lloyd.)] + +=321. Partial xerophytes.=—Plants exposed to periodic and occasional +droughts frequently provide against hard times by laying up stores +of nourishment in bulbs and rootstocks and retiring underground +until the stress is over. This is known as the _geophilous_, or +earth-loving, habit. Others, as some of the lichens, and the little +resurrection fern (_Polypodium incanum_, Figs. 419, 420), so common +on the trunks of oaks and elms in the Southern States, make no +resistance, but wither away completely during dry weather, only to +waken again to vigorous life with the first shower. + +[Illustration: FIGS. 419, 420.—A resurrection fern: 419, in dry +weather; 420, after a shower.] + +=322. Physiological xerophytes.=—Plants growing in thin or poor +soil, such as that on denuded hillsides, fresh railroad cuts, and +newly graded streets, are apt to take on a more or less xerophytic +character, even though there may be no lack of moisture. Such soils +are called “new” because the mineral elements in them have not +been exposed long enough to have become decomposed and mixed with +humus, and the vegetation that first populates them has to do the +pioneer work of disintegrating and impregnating the substratum with +humus. For similar reasons the vegetation of sandy bogs and sea +beaches, owing to the poverty of the soil in nitrogenous matter, +usually develops xerophyte adaptations, even though there may be a +superabundance of moisture. Plants growing on high mountain tops and +in cold arctic bogs take on the same characteristics (Fig. 410). +Such situations are said to be “physiologically dry,” because the +moisture they have is not in a condition to be readily absorbed. The +vegetation of arctic regions suffers more from physiological drought +than from cold. + +[Illustration: FIG. 421.—A halophyte swamp of mangroves. Notice the +tangle of adventitious prop roots assisting in the work of absorption +from the brackish marsh soil. (_From_ Mo. Botanical Garden Rep’t.)] + +=323. Halophytes= include plants growing by the seashore and +the vegetation around salt springs and lakes and that of alkali +deserts. Seaweeds are in a sense halophytes, since they live in salt +water, but as they are true aquatic plants and exhibit many of the +peculiarities of hydrophytes in their mechanical structure, they are +classed with them. The name _halophyte_ applies more particularly to +land plants that have adapted themselves to the presence in the soil +or in the atmospheric vapor, of certain minerals, popularly known as +salts, which cause them to take on many xerophyte characteristics. +The reason for this, as was shown in Exp. 39, is because the mixture +of salt in the water of the soil increases its density so that it +is difficult for the plant to absorb as much as it needs, and thus +halophytes are living under “physiologically” xerophyte conditions. +If you have ever spent any time at the seashore, you cannot fail +to have observed the thick and fleshy habit exhibited by many +of the plants growing there, such as the samphire, sea purslane +(_Sesuvium_), and sea rocket (_Cakile_). A form of goldenrod found by +the seashore has thick, fleshy leaves, and is as hard to dry as some +of the fleshy xerophytes. + +Another characteristic of desert plants that is common also to +seaside vegetation is the frequent occurrence of a thick, hard +epidermis, as in the sea lavender and saw grass. The live oaks, trees +that love the salt air and never flourish well beyond reach of the +sea breezes, have small, thick, hard leaves, very like those of the +stunted oaks that grow on the dry hills of California. The presence +of spines and hairs, it will be observed, is also very common; +_e.g._ the salsola, the sea oxeye, and the low primrose (_Œnothera +humifusa_). In other cases the leaf blades are so strongly involute +or revolute (202) as to make them appear cylindrical. All these, it +will be observed, are xerophyte adaptations, and the object in both +cases is the same—the conservation of moisture. + +=324. Mesophytes.=—These embrace the great body of plants growing +under the ordinary conditions of temperate regions, which may vary +from the liberal water supply of low meadows and shady forests to +the almost desert barrenness of dusty lanes and gullied, treeless +hillsides. The forms and conditions they present are so varied that +it would be impracticable to consider them all in a work like this, +but they may be summed up under the two general heads of (1) _open +ground_ and (2) _woodland_. Under the first are included: (_a_) all +cultivated grounds—fields, meadows, lawns, pastures, and roadsides, +with their characteristic shrubs, flowers, and grasses; (_b_) heaths +and plains of northern or alpine regions, with their low, stunted +perennials and bright, but fugacious, flowers. Under the second are +classed all woods, thickets, and copses, with the shrubs and herbs +that form their undergrowth. These may be grouped in three main +divisions: (_c_) mixed forests of maple, ash, oak, hickory, birch, +sweet gum, etc.; (_d_) pure forests of pine, balsam, fir, cypress, +and the like; and finally (_e_), the perennial splendors of the +tropical forest, where the vegetation of the globe reaches its climax +in luxuriance and variety of growth. + + + Practical Questions + + 1. Why do florists cultivate cactus plants in poor soil? (320.) + + 2. What would be the effect on such a plant of copious watering and + fertilizing? + + 3. Why must an asparagus bed be sprinkled occasionally with salt? + (323.) + + 4. If a gardener wished to develop or increase a fleshy habit in a + plant, to what conditions of soil and moisture would he subject it? + (320, 323.) + + 5. What difference do you notice between blackberries and + dewberries grown by the water and on a dry hillside? + + 6. Are there corresponding differences in the root, stem, and + leaves of plants growing in the two situations, and if so account + for them? + + 7. When a tract of dry land is permanently overflowed by the + building of a dam or levee, why does all the original vegetation + die, or take on a sickly appearance? (319.) + + 8. Should plants with densely hairy leaves be given much water, as + a general thing? (202, 320.) + + 9. A farmer planted a grove of pecan trees on a high, dry hilltop; + had he paid much attention to ecology? Give a reason for your + answer. + + 10. Why do the branches of trees often die, or fail to develop, on + the windward side? (314.) + + 11. Why do trees grown in dry soil have harder wood than the same + kind grown in wet soil? (123, 318.) + + + III. ZONES OF VEGETATION + +[Illustration: FIG. 422.—A pioneer colony of sumac growing on a +railroad cutting. (_From_ a photograph by J. M. Coulter.)] + +=325. The origin of vegetable zones.=—The terms “zone” and “zonation” +are used to express a general tendency of plant societies and +formations to distribute themselves in more or less regular belts +or strata, relatively to the varying intensity of the prevalent +ecological factor of their habitat. In almost every locality there +exists some special feature—a pond, a brook, a small ravine, an +isolated hilltop, a deserted quarry, a gravel pit, or a railroad +cut,—sufficiently distinct from the general surroundings to exercise +a perceptible control over the vegetation in its immediate vicinity, +and thus to become the starting point of a series of plant zones +that mark the decreasing influence of the factor concerned, by +their change of character as they recede from its point of greatest +intensity. Starting from a barren, exposed hilltop, for example, +with a covering of dry broom sedge (_Andropogon_) and fleabane, we +encounter next an almost desert zone of washed and gullied slopes +in whose hard, sunbaked soil nothing but a few scrub pines and +brambles can gain a foothold. This will, perhaps, be succeeded, by a +straggling belt of sassafras, sumac, and buckthorn, mixed with cat +brier and blackberry canes, beyond which, at the foot of the hill, +begins a stretch of meadow, or a bit of woodland crossed by a brook, +or hollowed into a boggy depression. From this new factor originates +a second series of zonations, passing through all the stages of bog, +swamp, shade, and sun plants, back to the prevailing type of the +region. Moisture is really the controlling factor in both cases, its +influence in the first being negative,—that is, inversely,—and in the +other, positive, or directly proportioned to the quantity present. + +=326. Direction of zonation.=—When the direction in which the +controlling factor changes is horizontal, as with soil and water, +the zonation will be _horizontal_; when, as in the case of light, +it is vertical, the zonation or stratification will be _vertical_. +Examples of this can be observed in the growth of almost any forest +area, the natural order of succession being: (1) a ground layer of +mosses and fungi; (2) low, creeping vines,—partridge berry, trailing +arbutus, twinflower (_Linnæa_); (3) small ferns and low flowering +herbs—pyrola, clintonia, trillium; (4) a zone of tall herbs and low +bushes—royal fern, cohosh (_Actæa_), blueberries; (5) tall herbs and +shrubs, small trees, and climbing vines—kalmia, dogwood, farkleberry, +smilax, Virginia creeper; (6) tall treetops towering up into full +sunlight. + +When the physical cause of intensity is a central area, such as a +pond or a hilltop, the zonation will be _concentric_; that is, the +different belts will succeed each other in widening circles more +or less complete. Where the controlling cause extends in a line, +as a river, or a chain of mountains, the zones run in parallel +belts on each side of it, and the zonation is _bilateral_. In any +case, however, it is seldom regular, being frequently broken and +interrupted through the intervention of other factors. Nor must +precisely the same kind of plants be always looked for in similar +situations, though their place is usually occupied by kindred species +and genera. The common pitch pine, for instance, of the Northern sand +barrens is represented in sandy districts farther south by the tall, +long-leaved pine, a kindred species. + +=327. Succession.=—Zonation is a regular succession of different +kinds of plants in space; there is also an analogous succession in +time, as, when the vegetation of a locality is killed off by fire or +other cause, plants of an entirely different character will nearly +always spring up to occupy its place. A forest of pine, for instance, +is rarely followed by conifers, but by a growth of hardwood trees, +and _vice versa_—nature thus giving an impressive example as to the +effectiveness of a rotation of crops. + +[Illustration: FIG. 423.—A thicket of pines that has succeeded a +mixed growth of hard wood trees.] + +Succession may be influenced by a variety of causes. Two of the most +efficient are: (1) the exhaustion of the soil by the long-continued +growth of one formation (60), thus causing a deficiency of mineral +material suited for the support of plants of that kind; (2) the +migration of new species into the denuded territory where those which +have different requirements as to mineral nutrients from the former +inhabitants will, other things being equal, have the best chance to +succeed. + +[Illustration: FIG. 424.—A successful invasion—Japanese honeysuckle +covering the banks of a ravine and climbing over shrubs and tree +tops.] + +=328. Invasion.=—A rapid and widespread occupation of any territory +by a new species is called an _invasion_. Notable examples of +invaders are those of the Russian thistle in the northwestern states +of the Union, and the “bitterweed” (_Helenium tenuifolium_) that +has almost driven out the hardy dog fennel (_Anthemis cotula_) +which formerly held undisputed possession of arid places throughout +the South Atlantic states. A still more remarkable instance is +the invasion of the Japanese honeysuckle (_Lonicera Japonica_), +originally introduced for ornament, but which has naturalized itself +within the last thirty years and overrun waste places everywhere, +from the Gulf to the Potomac, with a vigor and luxuriance equaled by +few of our native species. As its beauty and fragrance are even more +conspicuous in a state of nature than under cultivation, and as it +can, moreover, be made very useful in stopping gullies and washes, +its phenomenally rapid occupation of so large a territory has caused +no alarm and consequently attracted little attention. + +=329. Climatic zones.=—These are more general groupings than those +we have been considering. They follow in a rough way the parallels +of latitude, and are classed accordingly as: (1) tropical; (2) +subtropical; (3) temperate; (4) boreal or (on mountains) subalpine; +(5) arctic or (on high mountains) alpine. Taking the cultivated +plants of our own country by way of illustration, we have the +subtropical zone, embracing Florida and the southern portion of the +Gulf states, where sugar cane, rice, and tropical fruits are the +staple crops. Then comes the temperate zone, with three agricultural +subdivisions: (_a_) the great cotton belt, with Indian corn, sweet +potatoes, and the peach, melon, and fig as secondary products. +Farther north, in the Central and Middle Atlantic states, we find +(_b_) the region of maize, hemp, and tobacco, with grapes, apples, +pears, cherries, and a great variety of garden vegetables as side +crops. Finally comes (_c_) the great wheat-growing region of the +North, with buckwheat, hay, and Irish potatoes as subsidiary crops. + +Technically, the distribution of the natural zones of vegetation from +south to north is classed under the three general heads of Forest, +Grass Land, and Arctic Desert, with numerous subdivisions in each. + +=330. Boundaries of the zones.=—While the broad continental zones +of vegetation follow, in a general way, the climatic zones outlined +above, they are not sharply defined, but run into each other and +overlap in various degrees, so that a map depicting the range of +vegetation in any wide area would show a marked deviation from those +of latitude. Various other geographical factors, such as mountain +ranges and bodies of water, influence the direction and character of +the prevailing winds and rains, and through them the moisture and +temperature, to so great an extent that they become the controlling +factors over wide areas. In countries bordering on the sea, the coast +line always marks a belt of its own, and on the sides of a mountain +range, all the climatic zones from the equator to the pole may be +repeated during an ascent of a few miles. + +In our own country, where the mountain chains and coast lines run +approximately north and south, the great continental zones have been +superseded, for all practical purposes, by four regional divisions +running almost at right angles to them. These are, disregarding minor +subdivisions:— + +(1) The Forest region, occupying the eastern and south central +portion of the Union. In classifying this territory as forest, it is +not meant to imply that it is now, or ever was, one unbroken jungle, +like parts of central Africa, but that it combines the conditions +most favorable to a vigorous and varied forest growth. + +(2) The Plains region, extending from the very irregular western +boundary of the forest region to the Rocky Mountains. + +(3) The Rocky Mountain region, including the Rockies and the Sierra +Nevadas with the desert area between them. + +(4) The Pacific Slope, a narrow strip between the Sierras and the +Pacific Ocean. + +[Illustration: PLATE 15.—This giant tulip tree is a relic of the +primitive forest. It is twenty-seven feet in circumference, at a +distance of four feet from the ground. Notice the sharp elbows of +the large boughs, a mode of branching characteristic of this kind of +tree.] + +The boundaries of these regions, like those of the great continental +zones, overlap in various ways, the plants of one region often +appearing in another, like an arm of the sea projecting into the +land. But the district where any class of plants reaches its highest +development is its proper habitat, and as a general thing the one +where its cultivation pays best. It would be a waste of time and +money to try to raise cotton in Maine, or cranberries in Georgia. + + + Practical Questions + + 1. Does the native wild growth of a region furnish any indication + of the kind of crops which could be successfully grown there? (325, + 326.) + + 2. Can you give a reason why the zones of cultivation may, in some + cases, be more extensive than the natural range of wild plants in + the same region? (262, 265.) + + 3. Can you give reasons why the reverse may sometimes be true? + (261, 284.) + + 4. What crops are raised in different parts of your own state? + + 5. Name some of the native plants characteristic of different parts + of your state. What are its principal plant formations? + + + Field Work + + 1. Ecology offers the most attractive subject for field work of all + the departments of botany. It can be studied anywhere that a blade + of vegetation is to be found. In riding along the railroad, there + is an endless fascination in watching the different plant societies + succeed one another and noting the variations they undergo with + every change of soil or climate. + + 2. Students in cities can find interesting subjects for study in + the vegetation that springs up on vacant lots, around doorsteps + and area railings, and even between the paving stones of the more + retired streets. On a vacant lot near the public library in Boston, + over thirty different kinds of weeds and herbs were found, and in + the heart of Washington, D.C., on a vacant space of about twelve by + twenty feet, nineteen different species were counted. Just where + such things come from, how they get into such positions, and why + they stay there, will be interesting questions for city students to + solve. + + 3. But the country always has been and always will be the happy + hunting ground of the botanist. All the factors considered in the + two preceding sections can hardly be found in any one locality, but + by selecting areas traversed by brooks, or by gullies and ravines, + very marked changes in the character of vegetation may often be + observed. Barren, sandy, or rocky soils, the sunbaked clay of naked + hillsides, and the borders of treeless, dusty roads will offer + close approximations to xerophyte conditions. + + 4. If there are any bodies of water in your neighborhood, examine + their vegetation and see of what it consists. Notice the difference + in the shape and size of floating and immersed leaves and account + for it. Note the general absence of free-swimming plants in + running water, and account for it. Note the difference between + the swamp and border plants and those growing in the water, and + what trees or shrubs grow in or near it. Compare the vegetation of + different bogs and pools in your neighborhood, and account for any + differences you may observe. Compare the water plants with those + growing in the dryest and barrenest places in your vicinity, note + their differences of structure, and try to find out what special + adaptations have taken place in each case. Make a list of those in + each location examined that you would class as pioneers. + + 5. Draw a map of the vegetation of some locality in your + neighborhood that presents a variety of conditions, such as a + steep hillside, a field or meadow traversed by a brook, the slopes + and borders of a ravine, or the change from cultivated ground to + uncultivated moor or woodland. Represent the different zones and + formations by different colored inks or crayons, or by different + degrees of shading with the pencil. + + 6. Draw a map of your state showing the different agricultural + regions, as indicated by the character of the cultivated plants in + each; use different colors, or light and dark shading, to define + the boundaries. Notice any irregularities of outline and account + for them—whether due to soil, moisture, geological formation, + winds, or temperature. What is the controlling factor of each + region? + + + + +CHAPTER X. CRYPTOGAMS + + + I. THEIR PLACE IN NATURE + +=331. Order of development.=—All the forms that have hitherto claimed +our attention belong to the great division of Spermatophytes, or +seed-bearing plants, designated also as _Phanerogams_, or flowering +plants. They comprise the higher forms of vegetable life, and because +they are more conspicuous and better known than the other groups, +they have been taken up first, since it is more convenient, for +ordinary purposes, to work our way backward from the familiar to the +less known, rather than in the reverse order. + +But it must be understood that this is not the order of nature. The +geological record shows that the simplest forms of life were the +first to appear, and from these all the higher forms were gradually +evolved. There is no sharp line of division between any of the orders +and groups of plants, but the line of development can be traced +through a succession of almost imperceptible changes from the lowest +forms to the highest, and it is only by a study of the former that +botanists have come to understand the true nature and structure of +the latter. + +=332. Basis of distinction.=—_Cryptogams_, or seedless plants as +a whole, are distinguished from the phanerogams by their simpler +structure and by their mode of propagation, which in the former +is by means of spores, while in the phanerogams it is by seeds. A +spore is a simple organic body, consisting usually of a single cell +which separates from the parent plant at maturity and gives rise to +a new individual. A seed is a complicated, many-celled structure, +containing within itself the rudimentary structure of a new plant +already organized. + +Beginning with the simplest forms, cryptogams are grouped in three +great orders:— + +=333. I. Thallophytes=, or thallus plants.—This group takes its name +from the _thallus_ structure that characterizes its vegetation. In +its typical form, a thallus is a more or less flat, expanded body, of +which the lichens and liverworts offer familiar examples among land +plants, and the kelps and laminarias among seaweeds. It may be of any +size and shape, however, and sometimes consists of a mere filament, +as in the common brook silk, or even of a single cell (Fig. 429). +The term is applied in general to the simplest kinds of vegetable +structure, in which there is no differentiation of tissues, and no +true distinction of root, stem, and leaves. While it is not peculiar +to the thallophytes, it has attained its most typical development +among them, and the name is therefore retained as distinctive of +that group. It embraces two great divisions, the Algæ and Fungi. The +first includes seaweeds and the common freshwater brook silks and +pond scums, besides numerous microscopic forms whose presence escapes +the eye altogether, or is made known only by the discolorations and +other changes caused by them in the water. To the fungi belong the +mushrooms and puffballs, the molds, rusts, mildews, and the vast +tribe of microscopic organisms called _bacteria_, which are so active +in the production of fermentation, putrefaction, and disease. + +[Illustration: FIG. 425.—A seaweed with broad, expanded thallus.] + +[Illustration: FIG. 426.—Anthoceros, a liverwort with flat, spreading +thallus.] + +=334. II. Bryophytes=, or moss plants.—This group likewise contains +two main divisions, Mosses and Liverworts. Familiar examples of the +latter are the flat, spreading green plants, bearing somewhat the +aspect of lichens, met with everywhere on wet rocks and banks around +shady watercourses. The name is a reminiscence of their former use in +medicine as a specific for diseases of the liver, and not, as in the +case of the liver leaf, of a fancied resemblance to that organ. + +Mosses are one of the best defined of botanical orders, and are +easily recognized by their slender, leafy fruiting stalks, growing +usually in dense, spreading mats, and presenting every appearance of +a highly organized structure, well differentiated into root, stem, +and leaves. + +The liverworts represent the more primitive division of the group, +and in some of their forms approach so near the thallophytes that it +is not difficult to recognize them as connecting links in the same +chain of life. Their relationship to the next higher group is not +clear, but while they represent a more primitive stage of evolution +than the mosses, the development of the latter has followed a course +divergent from the main line of evolutionary progress. + +[Illustration: FIG. 427.—A shoot of peat moss with ripe spore fruits, +_f_, _f_.] + +[Illustration: FIG. 428.—A common fern (_Polypodium vulgare_).] + +=335. III. Pteridophytes=, or fern plants, are classed roughly in +the three divisions of ferns, horsetails, and club mosses. They +differ greatly in structure, but all possess a vascular system, and +a well-organized structure of root, stem, and leaves. They rank next +to the spermatophytes in the order of development, and the group is +of especial interest on account of its relationship to the higher +plants. One of its divisions, the club mosses, has probably given +rise to at least one section of the gymnosperms, while the ferns are +regarded as the ancestors of the true flowering plants, which make +up the great class of angiosperms, and represent the highest type of +evolution yet attained in the vegetable kingdom. + + + II. THE ALGÆ + + MATERIAL.—Simple forms of green algæ can be found on the shady side + of tree trunks, damp walls, old fence palings, and the outside of + flowerpots. _Pleurococcus_, one of the commonest kinds, occurs as a + green, powdery mat or felt in damp places, and is often accompanied + by _protococcus_, another good specimen for study. _Spirogyra_ and + other filamentous algæ can be found in stagnant pools and ditches + and in old rain barrels. + + APPLIANCES.—Eosin solution, nitric acid, alcohol, iodine solution; + a white china plate; a hand lens; a compound microscope, and slides. + +=336. Variety of forms.=—This group embraces plants of the greatest +diversity of form and structure, from the minute volvox and desmids +that hover near the uncertain boundaries dividing the vegetable from +the animal world, to the giant kelps of the ocean, which sometimes +attain a length of from six hundred to one thousand feet. They are +usually classed according to their color, as green, brown, and red +algæ, including various subdivisions of each group. They all contain +chlorophyll, by means of which they manufacture their own food, +though in the red and brown divisions it is masked by the presence of +other pigments—an adaptation to the modified light that reaches them +at various depths under water. With few exceptions they can live only +in the water, and unlike any other form of plant life, attain their +highest development in the salty depths of the ocean. The freshwater +forms are small and inconspicuous, and generally of a more simple +type than the seaweeds. The great majority of them belong to the two +classes of green and blue-green algæ. The former is believed to have +furnished the type from which the higher plants have been evolved. + +[Illustration: FIG. 429.—Three stages in the division of a one-celled +alga (_Glœocaspa polydermatica_): _A_, division of a cell just +beginning; _B_, division further advanced; _C_, four cells after +division, remaining in contact.] + +=337. Study of a one-celled alga.=—Put a little of the green algæ +in water on a glass slide. Hold up to the light, or over a sheet +of white paper, and examine with a hand lens; then place under +the microscope. It will probably be found to contain a number of +minute organisms, but the pleurococci can be recognized as small +round bodies of a bright green color, some of them separate, others +adhering together in groups of two, four, or more, with the sides +that are in contact slightly flattened. Each of these bodies is an +individual plant consisting of a single cell, whence they are said +to be _unicellular_. Draw one of the single cells and one of the +groups, or colonies, as they appear under the microscope. Try to +make out the cell wall and the nucleus, and label all the parts (see +7). If you have any difficulty in distinguishing the cell wall, drop +a little glycerine or salt water on the slide. This will cause the +cell contents to shrink by osmosis (56, 59). Can you make out the +structure of the cell colonies? They have resulted from the peculiar +mode of multiplication that prevails among this class of plants. A +cell elongates, contracts in the middle, and divides into two parts, +each of which becomes an independent plant like the mother cell. See +if you can find one in the process of division. The daughter cells +repeat the process, each one giving rise to two new individuals, and +so on indefinitely. The new cells do not always separate immediately +on their formation, but frequently adhere together for a time, in +colonies, before falling away and beginning an independent existence. + +=338. Reproduction by fission.=—This kind of reproduction is called +_fission_, or cell division, and marks a very primitive stage of +development. Under stress of adverse conditions the cells formed +by division may remain inactive for a time. They are then called +_resting spores_, and when more favorable circumstances arise, they +begin again their work of reproduction and growth as actively as ever. + +=339. Meaning of the name.=—The suffix _coccus_ is a Latin noun +(plural _cocci_) meaning a grain or berry, and is a general term +applied to any small, round organism consisting of a single cell; +hence, _micrococcus_, a minute round body; _protococcus_, a primitive +form, or prototype of one-celled bodies; and _pleurococcus_, which +may be freely translated “a one-sided little round body,” from the +flattening of the adjacent sides during fission—_pleuro_ meaning +lateral, or pertaining to the side. + +It is important to remember this definition, as the term _coccus_ +is of very frequent occurrence in works of biology, as a suffix for +designating small round bodies of various kinds. + +=340. Examination of a filamentous alga.=—Place on a white dish a +few drops of water containing some of the green pond scum common in +stagnant pools and ditches. Examine with a hand lens; of what does +it appear to consist? Are the filaments all alike, or are they of +different lengths and thickness? Soak a number of them in alcohol for +half an hour and examine again; where has the green matter gone? Do +these algæ contain chlorophyll? (336; Exp. 65.) This class are called +filamentous algæ on account of their slender, threadlike thalli, +which look like bits of fine floss floating about in the water. The +bubbles of oxygen which they sometimes give off in great abundance +cause the frothy appearance that has given rise to their popular +name, “frog spit.” + +[Illustration: FIGS. 430, 431.—_Spirogyra_ (magnified): 430, two +filaments beginning to conjugate; 431, formation of spores.] + +=341. Spirogyra.=—The filamentous algæ are very numerous, and a +drop of pond scum will probably contain several kinds. At least +one of these, it is likely, will be a _Spirogyra_, as this is one +of the commonest and most widely distributed of them all. Place a +filament under the microscope and notice the spiral bands in which +the chlorophyll is disposed within the cells. It is from this spiral +arrangement that the species takes its name. Do you notice any +roundish particles inclosed in the chlorophyll bands? Test with a +little iodine solution and see what they contain. Each filament will +be seen, when sufficiently magnified, to consist of a number of more +or less cylindrical cells joined together in a vertical row, and thus +forming the simple threadlike thallus which characterizes this class +of algæ. Physiologically, each cell is an independent individual, and +often exists as such. Can you see the cell nucleus? If not, place a +few filaments in a solution of eosin and add a drop of acetic acid to +give the solution a pale rose color. After twenty to thirty minutes, +examine again; the nucleus will be stained a deep red. If you can +find an unbroken filament, examine both ends to see whether there is +any differentiation of base and apex. + +=342. Conjugation.=—See if you can find two filaments sending out +lateral protuberances toward each other. Watch and notice that after +a time these projections come together and unite by breaking down +the cell walls dividing them, the protoplasm in each contracts, the +contents of one pass over into the other, and the two coalesce, +forming a new cell but little, if any, larger than the original +conjugating bodies. This cell germinates under favorable conditions +and produces a new individual. This method of reproduction is known +as _conjugation_. The cells thus produced by the union of the +contents of two separate cells may either germinate at once, and give +rise to new individuals, or remain quiescent for a time, as resting +spores. + + + Practical Questions + + 1. Are any of the green algæ parasitic? How do you know? (186, 336.) + + 2. Why is their presence in water regarded as denoting unhygienic + conditions? + + 3. Mention some of the ways in which their presence may contribute + to the contamination of drinking water. + + 4. Refer to Exp. 66, and account for the bubbles and froth that + usually accompany these plants in the water. + + 5. Can you suggest any other causes than the evolution of oxygen + that might produce the same effect? + + 6. Is the presence of these gas bubbles of any use to floating + plants? + + + III. FUNGI + +[Illustration: FIG. 432.—A common form of mold, magnified, showing +thallus modified into a fibrous mycelium: _a_, _a_, spore cases; _b_, +mycelium. (_After_ KOPF, in part.)] + +=343. Classification.=—In the fungi the thallus structure is greatly +modified, appearing usually as a network of fine threads called the +_mycelium_ (pl., _mycelia_), from a Greek word meaning “fungus” +(369). These plants are all, with a few doubtful exceptions, +parasites or saprophytes which contain no chlorophyll and are +incapable of supporting an independent existence. Biologists are +divided as to their position in the genealogical tree of life. +The weight of authority at present inclines to the view that they +are degenerate forms derived from the algæ, but they have been so +modified by their parasitic habits as to render their position in the +general scheme of life a doubtful one. They represent an offshoot, +or side branch, as it were, of the great evolutionary line, and so +may be considered for the present as standing apart in a class by +themselves. + +=344. Numbers and variety.=—Fungi exceed every other class of +living organisms both in the number of species and of individuals +composing them. They include such diverse forms as bacteria, molds, +rusts, mildews, mushrooms, and the like, ranging in size all the way +from the giant puffball, a foot or more in diameter, to the almost +inconceivably minute influenza bacillus, of which nearly two thousand +million can inhabit a single drop of water without inconvenient +crowding! + +[Illustration: FIG. 433.—Cephalothecium, a fungus parasitic on +rosehips—greatly magnified. (_From_ Mo. Botanical Garden Rep’t. +Photographed by Hedgcock.)] + +=345. The parasitic habit.=—But while their life history is obscure +and hard to trace, the fungi are, as a class, well differentiated by +their parasitic habit. They contain no chlorophyll, can manufacture +no food, and consequently have to obtain it ready-made from the +tissues of living or dead animals and plants. On this account they +are active agents in the production of disease and decay, especially +certain of those manifold forms that have been grouped together +under the general head of bacteria. While not responsible for all +the disease known to be caused by living organisms,—some very +serious ones, such as malaria and cattle fever, being due to animal +parasites,—the majority of those that have been most carefully +investigated are traced to the bacteria, or other fungi. After any +of these parasites have found a lodgment in the body of an organism +whose tissues furnish them a congenial habitat, they multiply with +enormous rapidity, and through the action of certain poisons called +_toxins_, which they excrete, give rise to the most destructive +diseases in both animals and plants; and no rational sanitary science +is possible without a knowledge of their habits and life history. Add +to the vast amount of human suffering that is to be laid at their +door the economic damage done by rust and smut fungi, by molds and +blights and mildews, and we shall be tempted to conclude that the +“battle of life” is largely a struggle against these invisible foes. + +[Illustration: FIGS. 434-437.—Disease-producing bacteria: 434, +bacteria of consumption (_Bacillus tuberculosis_); 435, cholera +bacillus; 436, bacilli of anthrax, showing spores; 437, typhoid +bacillus.] + +=346. Useful fungi.=—Not all fungi, however, are injurious. On the +contrary, the great majority of them are harmless, and very many +kinds are positively beneficial to man. Without the yeasts and +bacteria of fermentation we could not have our bread and cheese. +Other forms are active agents in the fertilization of soils, it +having been estimated that there are 100,000 or more of these +infinitesimal laborers at work in every cubic centimeter (about ¹⁄₁₆ +of a cubic inch) of virgin soil! Even the bacteria of putrefaction, +which we are accustomed to regard as the embodiment of all that is +foul and loathesome, are engaged in an unceasing work as scavengers, +without which life would no longer be possible on our globe, as will +be shown in the following section. + + + A. BACTERIA + + MATERIAL.—A vessel of water in which hay has been left to soak for + several hours; a freshly boiled potato. + + APPLIANCES.—A double boiler for sterilizing; a number of clean + glass jars and bottles; cotton wool for stoppers; a compound + microscope. + + CULTURE MEDIUMS.—A freshly boiled potato answers very well for + ordinary purposes. “Bread mash” can be made by drying some bread + crumbs in an oven, then mashing and mixing them to a paste with + boiling water; sterilize by three successive heatings in a double + boiler. A sterilized preparation of gelatine solution is the medium + most commonly used. + +=347. How to obtain specimens for observation.=—While bacteria are +plentiful almost everywhere, it is not always easy to capture them +just when and where you want them. For this purpose, put some hay +in water and leave in a warm place away from the light until the +liquid becomes cloudy or a film forms on the surface. This will show +that bacteria are present. If it is desired to study any particular +kind of bacterium, inoculate one of the culture mediums described +under “material,” or a few drops of sterilized extract of beef, with +a small quantity of the substance to be examined, or with dust or +scrapings from the locality under consideration. + + EXPERIMENT 93. BY WHAT MEANS ARE BACTERIA COMMONLY DISTRIBUTED?—Put + a slice of freshly boiled potato into each of three glass tumblers + and cover with a filter of cotton wool held in place by tying + tightly with a cord, or by an elastic band. Set them all in a + vessel of water, bring it to a boil, and keep at that temperature + for half an hour, to sterilize the air in the tumblers. When they + have cooled, lift the cotton from (1) for a minute or two and then + replace. Carefully pass the tip of a medicine dropper through the + filter of (2) so as to prevent the entrance of unsterilized air, + and put on the slice of potato a small quantity of the bacterial + liquid prepared as directed in the last paragraph. Leave (3) + unopened. Keep all together in a warm, dark place and observe at + intervals of from 12 to 24 hours. Do any bacteria appear in (3)? + Do any appear on the potato in (2), where the liquid was dropped? + Are they more, or less abundant than in (1)? Since cotton wool is + entirely impervious to the smallest microörganisms known, would you + judge from this experiment that bacteria can get into any place + unless carried there by the air, or by some other means? + + EXPERIMENT 94. CAN BACTERIA BE CARRIED BY PURE AIR?—On a warm (and + preferably cloudy) day, put a slice of potato on a plate, and leave + uncovered in an unused room or closet, free from dust, and kept + carefully closed. Put another slice arranged in exactly the same + way in an open window on a dusty street, or in a room that is used + and daily swept and dusted. Do bacteria appear in the first plate? + In the second? Is air free from dust a good conveyor of bacteria? + + EXPERIMENT 95. WHAT CONDITIONS ARE FAVORABLE TO BACTERIAL + GROWTH?—Strain some of your culture liquid into half a dozen small + bottles of the same size, filling each about half full. Put (1) in + a dark, cool place—on ice, if the weather is warm; (2) in a dark, + warm place; (3) in a warm, well-lighted place; into (4) put a drop + of carbolic acid, formalin, corrosive sublimate, or boracic acid, + and keep in a dark, warm place. Keep (5) in boiling water for half + an hour or more, and then place beside (2). Keep (6) in a freezing + mixture of salt and ice for several hours, then place with (2) and + (5). Examine all at intervals of from 12 to 24 hours. In which + bottles is the presence of bacteria indicated by cloudiness of the + contained liquid, or the formation of a surface film? In which do + they appear first? In which most abundantly? In which last, or not + at all? What is the effect of light and darkness on their growth? + Of heat and cold? Of disinfectants? Name the circumstances that + tend to hinder their growth, in the order of their efficacy. + +=348. Microscopic study of bacteria.=—Put a drop of hay infusion on a +slide and examine with the highest power of the microscope. You will +see a multitude of very small glistening bodies including different +kinds of bacteria, a majority of which are probably the hay bacillus, +_B. subtilis_, shown in Figs. 443, 444. Notice that some forms move +about freely, while others are non-motile. Which kind are the more +numerous? The motion may be either mechanical, resembling that of +the small dust particles we see dancing about in the sunshine, or +apparently voluntary, and caused by the vibration of little whiplike +cilia. Can you distinguish the two kinds? Try to make out clearly +the different shapes you see. Some appear as slender chains or +filaments, but this is due to the individual cells’ adhering together +for a time before breaking up and beginning an independent existence. +The small, rounded bodies, like a period (Fig. 438), are _cocci_; the +slender, rod-shaped ones—sometimes slightly curved (Fig. 440)—are +_bacilli_ (sing., _bacillus_); the comma-shaped ones, and those +generally showing a slight spiral curvature, are _vibrios_ (Fig. +441); the spirally twisted ones, like a corkscrew (Fig. 442), are +_spirilli_ (sing., _spirillum_). These are the principal forms which +it is important to distinguish and remember. The names are applied +very loosely, however, in practice, bacillus being often used as a +general term applicable to almost any kind,—the spirillum of cholera, +for instance, being commonly known as the cholera bacillus, while by +some authors vibrios are ranked as a variety of spirillum. + +[Illustration: FIGS. 438-442.—Typical forms of bacteria: 438, coccus +type; 439, the same, hanging together in chains; 440, rod-shaped +bacteria (bacillus type), the clear areas in some of these are +spores; 441, forms of vibrio; 442, forms of spirillum.] + +=349. Life history of a typical bacterium.=—A pure culture of the +_Bacillus subtilis_ can easily be obtained by boiling some of the +hay infusion for half an hour and then leaving in a warm place till +the usual indications of the presence of bacteria appear (347). +The spores of this micro-organism are so resistant that they can +withstand the temperature of boiling water for several hours, while +those of most other forms of bacteria are killed by a few minutes’ +exposure to it; hence, the crop that develops after boiling will +consist of a pure culture of the hay bacillus. + +[Illustration: FIGS. 443, 444.—Hay bacillus (_B. subtilis_): 443, a +portion of the film from the culture liquid, the black lines, _e_, +being bacteria in the vegetative state; 444, spore formation; _a_, +_d_, motile cells and chain of cells: _b_, non-motile cells; _c_, +spores and chain of spores from the film _e_.] + +In their active state these organisms will be seen to consist of +single-celled, rod-shaped bodies, about three or four times as long +as broad, and generally cohering in bands or filaments, as shown in +Fig. 444, _c_. The black dots within the cells are the spores. Each +individual bacterium produces but a single spore, or rather becomes +a spore itself, by the contraction of its contents and the formation +around them of a strong inclosing membrane. On germinating, the +spores give rise to little ciliated, one-celled organisms called +“swarm spores,” that swim about freely in the containing medium and +multiply rapidly for a time by cell division. After this they pass +again into the quiescent state, ready, whenever favorable conditions +arise, to begin anew the repetition of their life cycle, which is an +irregular alternation of cell division and spore formation. + +=350. Resistance of spores.=—Bacteriologists are not fully agreed as +to the cause of spore formation, some holding that it takes place +only when conditions are most favorable for bacterial growth, others +claiming the reverse. The consensus of opinion at present is toward +the view that the spores are a provision for tiding over periods of +stress and difficulty. They are capable of retaining their vitality +for a long time, and are much harder to kill than the bacterial +cells in their ordinary vegetative state, as was seen in the case of +the hay bacillus. The spores of one species of potato bacillus have +retained their vitality after four hours of boiling, and those of the +typhoid bacillus after continuous exposure to a freezing temperature +for more than three months. The majority of bacteria, in their +vegetative state, are, however, either killed or rendered inert by +temperatures ranging below 10° or above 50° centigrade—equivalent to +about 50° and 122° Fahrenheit, respectively. It is easy to see what +important bearing these facts have on the process of disinfection. + +=351. Reproduction and multiplication.=—The ordinary mode of +reproduction in bacteria, as in other unicellular organisms, is by +fission (337, 338). As each individual forms but a single spore, no +increase in numbers could take place by this means alone. Hence, +while the spores are an important factor in the preservation of +the species by continuing its existence under conditions which the +active organisms could not survive, their successful propagation +depends on their power of rapid multiplication by division. If +this process were to go on unchecked, every hour, in an unbroken +geometrical progression, the progeny of a single bacterium would, +in 24 hours, number nearly 17 million; in 25 hours, 34 million; in +26 hours, 68 million, and in five days they would cover the entire +surface of the globe, land and sea, to a depth of 3 feet! In ordinary +standard milk sold by dairymen, and containing, when examined, less +than 10,000 microbes to the cubic centimeter,—about 20 drops,—the +number was found to have increased after 24 hours to 600 million. +It is comforting to know, however, that the majority of these are +of the harmless kinds which are the active agents in the making of +buttermilk and cheese. + +The effects of their rapid multiplication will be better appreciated +when we consider that bacteria are the smallest of known living +creatures. If 1000 of the influenza bacilli were spread out in +a single layer with their sides touching, but not overlapping, +they would not take up more room than one of the periods used in +punctuating this book; and a coccus concerned in a tubercular disease +prevalent among cattle in South America has recently been discovered, +of which double that number could be accommodated in the same space. + +[Illustration: FIGS. 445, 446.—Milk (highly magnified): 445, pure, +fresh milk, showing fat globules; 446, milk that has stood for hours +in a warm room in a dirty dish, showing fat globules and many forms +of bacteria.] + +=352. Distribution of bacteria.=—Ordinary air, when free from +dust, contains, on the average, not more than five germs to the +liter—equal to about 1 for every 12 cubic inches. Pathogenic, or +disease-producing, germs seldom occur in ordinary fresh air, and +even when present are, under ordinary circumstances, harmful only to +people whose bodies, by reason of physical weakness or unhygienic +habits, offer a congenial soil for their multiplication. Numerous +instances are known in which perfectly healthy persons have carried +about infectious disease germs in their bodies and even transmitted +them to others without experiencing any inconvenience, or even being +aware of their presence. Among others, the germs of pneumonia, +diphtheria, and tuberculosis are often found in the mouth, nose, +and sputum of perfectly healthy persons. There are also a number +of bacteria that are regular inhabitants of the mouth, some of +which are the cause of decayed teeth and foul breath. One form of +bacterium, concerned in the production of inflammation and abscesses +(_Staphylococcus_) is so constantly present on the human epidermis +that one authority has declared it impossible to sterilize the +skin so thoroughly as to free it entirely of this microbe. It is +ordinarily not harmful unless it comes in contact with open wounds +and abrasions. + +=353. The economic importance of bacteria.=—It is hard to say +whether these organisms concern us most on account of the damages +attributable to them on the one hand, or the benefits we owe them +on the other. If they were all as harmful as the pathogenic kinds, +life would hardly be possible on the globe, while without their +presence life as we know it would have ceased to be possible long +ago. They are nature’s great army of scavengers, the sole agents of +decomposition, without which dead organic matter would be subject +only to the slow changes by which the rocks and mineral matter of the +earth’s crust are disintegrated, and the undecomposed bodies of the +vast procession of plants and animals that have existed since life +first began on our globe would long ago have cumbered its surface to +such an extent as to render impossible the continued development of +life such as we know. + +=354. Sterilization= is the process of ridding a substance of living +microörganisms. To do this effectively, the process must be repeated +several times at intervals, so as to give any spores that may have +survived previous applications time to pass into the vegetative +state, when their power of resistance is diminished and they are more +easily destroyed. The incubation period, as the time required for +the germination of the spores is called, is different for different +kinds of bacteria; hence the importance, from a sanitary point of +view, of a thorough knowledge of their life history. + +=355. Disinfection= is sterilization on a large scale, and the same +principles apply to both. Heat is the safest disinfectant for objects +that will bear it, if continued long enough and repeated often enough +at a sufficiently high temperature. Freezing will destroy some kinds +of germs and check or retard the development of nearly all, but +is not to be relied on as a permanent germicide, since even among +flowering plants there are many kinds, not only of seeds, but of +perennial vegetative forms that are capable of enduring an arctic +temperature of many degrees below freezing for long continued periods. + +Chemical disinfectants act usually as microbe poisons, and are +unsuitable as sterilizers for food, though valuable in the +purification of houses, clothing, and utensils—especially the +instruments employed in surgical operations. + +The prevention of the growth of bacteria, especially in wounds +and surgical incisions, whether by means of chemical or physical +agencies, is known as _antisepsis_. + + + Practical Questions + + 1. Why should a person recovering from an ague continue for some + time after to take quinine every third or every seventh day? (350, + 354.) + + 2. Name some of the principal diseases produced by bacteria. + + 3. What is the principle to be acted on in the avoidance of such + diseases? (Exps. 94, 95.) + + 4. Are the same means equally effective for prevention and for + cure? (354, 355; Exps. 93-95.) + + 5. Why is “fresh air” beneficial in a sick room? (352; Exp. 94.) + + 6. Does it act as a disinfectant, or as a mere diluent of the + infected air of the room? (352.) + + 7. Why ought preserved fruits and vegetables to be scalding hot + when put into the can? (355.) + + 8. Why is it necessary to exclude the air from them? (Exps. 93, 94.) + + 9. Reconcile question 8 with question 5. + + 10. Why does the use, for drinking purposes, of water that has been + boiled render a person less liable to infectious diseases? (355.) + + 11. Was the old-fashioned practice of handing the baby round to be + promiscuously kissed by friends and neighbors a good one for the + baby? (352.) + + 12. Why is the spitting habit to be condemned? The use of common + drinking cups in schoolrooms and other public places? (352.) + + 13. Is it proper from a sanitary point of view that roommates at + a boarding school, or even members of the same family, should use + soap, towels, and other articles of the toilet in common? (352.) + + + B. YEASTS + + MATERIAL.—A piece of fresh baker’s yeast, some warm water, and a + little honey or sugar solution; a pipette, or a medicine dropper; + three or four clean pint bottles or preserve jars. + + To raise a crop of yeast fungi for observation, rub one fourth of a + fresh yeast cake in water enough to make a paste; add one pint of + water, with a tablespoonful of honey or sugar, and stir well. + + EXPERIMENT 96. WHAT CONDITIONS FAVOR THE GROWTH OF YEAST?—Pour + equal parts of the liquid made as directed (see Material) into each + of three pint bottles, stopper lightly, and label. Put (1) in a + warm, dark place; (2) in a cool, dark place; and (3) in a bright + light in a warm place. Observe at intervals of a few hours the + changes that occur in each. Notice the bubbles that rise from the + liquid. In which bottle do they form most rapidly? Lower a lighted + match into it, or transfer some of the gas with a pipette into a + vessel containing limewater, and tell what it is. Taste some of the + fermenting liquid. Is it sweet? What has become of the sugar that + was put into it? + +=356. Yeasts and ferments.=—Yeasts belong to a very different order +of fungi from the bacteria, but on account of their simplicity of +structure and the similarity of their action to that of some of the +latter, it is usual to consider them together. They are the active +agents of fermentation, and include a large number of species. The +kind used for household purposes is the same as that employed in +making beer. Of this species there are many varieties, each one of +which gives a characteristic taste to the beer made from it; and +brewers, by paying attention to the cultivation of yeasts, give their +product the special flavors peculiar to the different brands. This +kind of yeast is not known to exist except in a state of cultivation, +and probably owes its survival and present condition of development +to a symbiosis with man, on account of its usefulness in bread +making, and still more, perhaps, to its part in the gratification of +his bibulous propensities, for among savage tribes the manufacture of +fermented liquors is practiced long before the wholesome art of bread +making. + +[Illustration: FIGS. 447-449.—Forms of common yeast (_Saccharomyces +cerevisiæ_): 447, brewers’ yeast; 448, household yeast (the large +grains are starch); 449, yeast from beer sediment, showing budding. +(Figs. 447, 448 × 250; Fig. 449 × 1270.)] + +There are other yeasts existing in a state of nature, such as those +on the surface of fruits, which cause the latter, under certain +circumstances, to ferment and decay. For this reason artificial +ferments are not needed in making wine and other alcoholic liquors +from fruits. Fermentation is also caused by certain forms of +bacteria, as in the formation of vinegar and the souring of milk. +Such bacteria often contaminate the yeast ferments. + +=357. Microscopic examination.=—Place a drop of the cultural +liquid on a slide and examine under the highest power of the +microscope. What do you see? These egg-shaped bodies are yeast +plants, unicellular organisms like the pleurococcus. Do you see any +chlorophyll? Are the yeasts parasitic? How do you know? What do they +live on? (Suggestion: What food substance that has disappeared was +put into the culture liquid?) In getting their nourishment from the +sugar, these fungi disintegrate it into alcohol and carbon dioxide, +which is a process of fermentation. It is the bubbles of gas that +were seen rising in the liquid which cause beer to effervesce and +bread to rise. They permeate the dough and by their expansion produce +the sponginess peculiar to leavened bread. Look for a cell with a +bud forming on it; from what part does it appear to grow? Where a +number of buds remain for some time attached to the mother cell (Fig. +449), they form a _colony_. Make a sketch of a single cell and of a +colony of two or more adherent ones, labeling all the parts. If the +cell wall cannot be made out clearly, run a little glycerine, or salt +water, under the cover glass with a medicine dropper. What causes the +contents of the cell to contract and leave the wall? (56, 59.) + +=358. Reproduction.=—From time to time buds break away from the +mother cell and form new individuals or colonies of their own. This +process is called multiplication by budding, and is only another form +of cell division. + +Whenever reproduction takes place by other means than seeds or +spores, it is said to be _vegetative_. This sort of reproduction +is not confined to unicellular plants, but exists also among the +phanerogams, the propagation of species by means of buds, tubers, +rootstocks, runners, grafting, and the like being variations of +the same process. On the other hand, yeasts and bacteria and the +unicellular algæ have the power, under extreme conditions, to form +resting spores, which sometimes lie dormant for years and resume +their activity when favorable conditions return. + + + Practical Questions + + 1. When is fermentation useful to man? + + 2. What is the effect on canned fruits and vegetables if yeast + cells get into them? + + 3. Why does milk turn sour in warm weather? (350, 351; Exp. 96.) + + 4. Why do buttermilk and clabber spoil if left standing too long? + (345, 356.) + + 5. What causes bread to be “heavy”? (356, 357.) + + 6. Why will dough not rise unless kept in a warm place? (Exp. 96.) + + 7. Why is beer kept cold during fermentation? (350, 356.) + + + C. RUSTS + + MATERIAL.—A leaf of wheat affected with red rust; a leaf or a stalk + with black rust. Some barberry leaves with yellowish pustules on + the under side, which under the lens look like clusters of minute + white corollas. These are popularly known as “cluster cups.” As the + spots on barberry occur in spring, the red rust in summer, and the + black rust in autumn, gather the specimens as they can be found, + and preserve for use. + +[Illustration: FIGS. 450, 451.—Leaf of wheat affected with orange +leaf-rust (_Puccinia rubigo-vera_), uredo stage: 450, upper side of +leaf; 451, under side.] + + The orange leaf, or brown, rust (_Puccinia rubigo-vera_) is more + common in some parts of the country than the ordinary wheat rust + (_Puccinia graminis_), but the two are so much alike that the + directions given will do for either. If the orange leaf-rust (so + named from its color, and not from any connection with orange + leaves, the logical relation of the words being orange leaf-rust, + and not orange-leaf rust) is used, the cups and pustules should be + looked for on plants of the borage family—comfrey, hound’s-tongue, + etc. The orange leaf-rust of apple is caused by a fungus which will + serve to illustrate the same class of parasites. The “teleuto” + stage of this will be found on cedar trees, in the excrescences + commonly known as “cedar apples”; the “cluster cups” on the leaves + of apple and haw trees affected with the disease. + +=359. Red rust.=—Uredo stage. Examine a leaf of “red rusted” wheat +under the lens, and notice the little oblong brown dots that cover +it. These are clusters of spore cases, and are the only part that +appears above the surface. Viewed under the microscope, the red rust +will be seen to consist of a mycelium (see Fig. 452), which ramifies +through the tissues of the leaf and bears clusters of single-celled +reddish spores that break through the epidermis and form the reddish +brown spots and streaks from which the disease takes its name. These +spores, falling upon other leaves, germinate in a few hours and form +new mycelia, from which, in six to ten days, fresh spores arise. +Formerly this was thought to complete the life history of the fungus, +to which the name of _Uredo_ was given. It is now known, however, +that the red rust is merely a stage in the life cycle of the plant, +and to this stage the old name uredo is applied, the spores being +called _uredospores_. + +=360. Black rust.=—Teleuto stage. Next examine with a lens a part +of the plant attacked by black rust. Do you observe any difference +except in the color? Do the two kinds of rust attack all parts +of the plant equally? If not, what part does each seem to affect +more particularly? At what season does the black rust appear most +abundantly? Place a section of the diseased part under the microscope +and notice that the difference in color is due to a preponderance +of long, two-celled bodies with very thick, black walls (Fig. 453). +These are called _teleutospores_, a word meaning “final spores,” +because they are formed only toward the end of the season. They are +developed from the same mycelium with the uredospores, and are not +a product of the latter, but collateral with them and belong to the +same stage in the life history of the fungus. After they appear, +the uredospores cease to be developed at all, and only the dark +teleutospores are produced. These remain on the culms in the stubble +fields over winter, ready to begin the work of reproduction in +spring. For this reason the teleutos are popularly known as “winter +spores” in contradistinction to the uredos, or “summer spores,” whose +activity is confined to the warm months. + +[Illustration: FIG. 452.—Uredo spores of wheat rust (_Puccinia +graminis_), magnified. (_From_ COULTER’S “Plant Structures.”)] + +[Illustration: FIG. 453.—Teleutospores of wheat rust, magnified. +(_From_ COULTER’S “Plant Structures.”)] + +[Illustration: FIG. 454.—Teleutospore germinating and forming +sporidia, _s_, _s_. (_From_ COULTER’S “Plant Structures.”)] + +It was formerly supposed that black rust was caused by a different +fungus from that producing red rust, and to it the name _Puccinia_ +was given. This has been retained as a general designation for all +fungi undergoing these two phases, and the particular form of fungus +that we are now considering is known in all its stages as _Puccinia +graminis_. + +=361. The nonparasitic stage.=—The formation of teleutospores +completes that portion of the life history of the fungus during which +it is parasitic on wheat and grasses of different kinds. In spring +they begin to germinate on the ground, each cell producing a small +filament, from which arise in turn several small branches. Upon the +tip of each of these branches is developed a tiny sporelike body +called a _sporidium_ (Fig. 454), which continues the generation of +the rust fungus through the next stage of its existence. The filament +which bears these sporidia is not parasitic, but when the sporidia +ripen and the spores contained in them are scattered by the wind, +there begins a second parasitic phase, which forms the most curious +part of this strange life history. + +=362. The æcidium.=—Examine next the under side of some barberry +leaves (or comfrey, etc., if orange leaf-rust is used) for clusters +of small whitish bodies that appear under the lens like little white +corollas with yellow anthers in the center. Examine a section of one +of these under the microscope and notice that the yellow substance +is composed of regular layers of colored spores. The corolla-like +receptacles containing them, popularly known as “cluster cups,” +are borne on a mycelium produced from the spores described in the +last paragraph. This mycelium is parasitic on barberry or other +leaves, according to the kind of fungus, and was long believed to be +a distinct plant, to which the name _Æcidium_ (pl., _Æcidia_) was +given. This term is now applied to the cluster cups, and those fungi +which at any period of their life history produce them are called +æcidium fungi. + +[Illustration: FIG. 455.—Section through a barberry leaf, showing on +the upper side two spermogonia, _s_, _s_; and on the under side, an +æcidium, _æ_.] + +=363. Spermogonia.=—On the upper surface of the leaves that bear +the æcidia, notice some small black dots hardly larger than pin +points, but which, when sufficiently magnified, appear as little +flask-shaped bodies (Fig. 455) under the epidermis. These are known +as _spermogonia_, or _pycnidia_. When mature, they break through +the epidermis so that the necks protrude, and discharge a quantity +of minute cells or spores, very like some that, later on, we shall +find playing an important part in the reproductive processes of +certain other fungi, and of mosses and liverworts. In the rust fungi, +however, their function is not understood. They may possibly be +survivals of organs which were once active in the life processes of +the plant, but have become useless under changed conditions. Do such +organs throw any light on the evolutionary history of plants? + +[Illustration: FIG. 456.—A species of “cedar apple” +(_Gymnosporangum_), showing the uredo-teleuto stage of the apple rust +fungus. (_From_ a photograph by Prof. F. E. Lloyd.)] + +=364. Connection between barberry and wheat rust.=—With the discharge +of the æcidium spores, the part of the life cycle of the fungus +spent on the barberry comes to an end, and it is ready to begin the +uredo-teleuto stage over again as soon as it finds a suitable host. +Where there are no barberries, it is capable of propagating without +them, either by adapting itself to some other host plant, or by +omitting the æcidium stage altogether. The parasitic habit being an +acquired one, the fungus, like some animal organisms that we know of, +can often be “educated” by force of circumstances into tolerating, +and even thriving upon, foods which under other circumstances it +would reject. The wheat rust is known to be capable of propagating +year after year in the uredo stage, the spores surviving through +the winter on volunteer grains and grasses; and in no other country +in the world does rust do greater damage to the wheat crop than in +Australia, where the barberry is practically unknown. This power of +accommodation possessed by many parasites is one of the difficulties +the agriculturist has to contend with in the development of rustproof +varieties. + +=365. Polymorphism.=—Plants that pass through different stages in +their life history are said to be _polymorphic_, that is, of many +forms. The habit is very common among the lower forms of vegetation. +The fact that one or more of the phases are sometimes omitted, as +the æcidium phase of wheat rust in warm climates, suggests the idea +that it may be of use in helping the plant to tide over difficult +conditions. Besides giving better chances of obtaining nourishment, +it probably has the same effect as cross fertilization among +flowering plants, in imparting increased strength and vitality to the +succeeding generation. Wheat rust produced from barberry æcidia is +said to be much more vigorous—and consequently more destructive—than +when derived from a uredo that has reproduced itself for several +generations. + +=366. The damage done by rust= to the host is through the destruction +of its tissues by the mycelium. The chlorophyll is destroyed so that +the plant can no longer manufacture food, and is too starved to +produce good grain. There are many varieties of wheat rust, which +have been found on twenty-seven different kinds of grain. Most +of them are specialized to a particular host plant and will not, +ordinarily (364), infest any other. Has this fact any bearing upon +the production of rustproof varieties? + + + Practical Questions + + 1. Is a farmer wise to leave scabby and mildewed weeds and bushes + in the neighborhood of his grain fields? (364, 365.) + + 2. Are there any objections to the presence of volunteer grain + stalks along roadsides and in fence corners during winter? (364.) + + 3. Should cedar trees be allowed to grow near an apple orchard? + Give a reason for your answer. (p. 317, Material.) + + 4. Should diseased plants be plowed under? (361.) + + 5. What disposition should be made of them? + + 6. Ought diseased fruits to be left hanging on the tree? + + 7. Why is it necessary to pick over and discard from a crate or bin + all decaying fruits and vegetables? + + 8. Does a rotation of crops tend to prevent the spread of disease + in plants? Give reasons for your answer. + + 9. Are rustproof varieties to be relied on indefinitely? (364.) + + + D. MUSHROOMS + + MATERIAL.—Any kind of gilled mushroom in different stages of + development, with a portion of the substratum on which it grows, + containing some of the so-called spawn. The common mushroom sold in + the markets (_Agaricus campestris_) can usually be obtained without + difficulty. Full directions for cultivating this fungus are given + in Bulletin 53 of the U. S. Department of Agriculture. From 6 to 12 + hours before the lesson is to begin, cut the stem from the cap of a + mature specimen, close up to the gills, lay it, gills downward, on + a piece of clean paper, cover with a bowl or pan to keep the spores + from being blown about by the wind, and leave until a print (Fig. + 466) has been formed. + +=367. Mushrooms and toadstools.=—The popular distinction which limits +the term “mushroom” to a single species, the _Agaricus campestris_, +and classes all others as toadstools, has no sanction in botany. All +mushrooms are toadstools and all toadstools are mushrooms, whether +poisonous or edible. The real distinction is between mushrooms and +puffballs, the former term being more properly applied to fungi which +have the spore-bearing surface exposed. + +=368. Examination of a typical specimen.=—The most highly specialized +of the fungi, and the easiest to observe on account of their size and +abundance, are the mushrooms that are such familiar objects after +every summer shower. The _gilled_ kind—those with the rayed laminæ +under the cap—are usually the most easily obtained. Specimens should +be examined as soon after gathering as possible, since they decay +very quickly. + +=369. The mycelium.=—Examine some of the white fibrous substance +usually called spawn through a lens. Notice that it is made up of +fine white threads interlacing with each other, and often forming +webby mats that ramify to a considerable distance through the +substratum of rotten wood or other material upon which the fungus +grows. This webby structure, often mistaken for root fibers, is +the thallus or true vegetative body of the plant, the part rising +above ground, and usually regarded as the mushroom, being only the +fruit, or reproductive organ. Place some of the mycelium under the +microscope and notice that it is composed of delicate filaments made +up of single cells placed end to end, as in Spirogyra (341). These +filaments are called _hyphæ_. + +=370. The button.=—Look on the mycelium for one of the small round +bodies called buttons (Fig. 457). These are the beginning of the +fruiting body popularly known as the mushroom, and are of various +sizes, some of the youngest being barely visible to the naked eye. +After a time they begin to elongate and make their way out of the +substratum. + +[Illustration: FIG. 457.—Mycelium of a mushroom (_Agaricus +campestris_), with young buttons (fruiting organs) in different +stages: 1, 2, 3, 4, 5, sections of fructification at successive +periods of development; _m_, mycelium; _st_, stipe; _p_, pileus; _l_, +gill, or lamina; _v_, veil.] + +[Illustration: FIG. 458.—Diagram of unexpanded _Amanita_, showing +parts: _a_, volva; _b_, pileus; _c_, gills; _d_, veil; _e_, stipe; +_m_, mycelium.] + +=371. The veil and the volva.=—Make a vertical section through the +center of one of the larger buttons after it is well above ground, +and sketch. Notice whether it is entirely enveloped from root to cap +in a covering membrane—the _volva_ (Fig. 458, _a_)—or whether the +enveloping membrane extends only from the upper part of the stem to +the margin of the cap—the _veil_ (Fig. 458, _d_); whether it has both +veil and volva, or finally, whether it is naked, that is, devoid of +both. + +=372. The stipe, or stalk.=—Notice this as to length, thickness, +color, and position; that is, whether it is inserted in the center +of the cap or to one side (excentric), or on one edge (lateral). +Observe the base, whether bulbous, tapering, or straight, and whether +surrounded by a cup, or merely by concentric rings or ragged bits +of membrane (the remains of the volva). Look for the _annulus_ or +ring (remains of the veil) near the insertion of the stipe into the +cap, and if there is one, notice whether it adheres to the stipe, or +moves freely up and down (Fig. 459, _a_); whether it is thick and +firm, or broad and membranous so that it hangs like a sort of curtain +round the upper part of the stipe (Fig. 467, _a_). Break the stem +and notice whether it is hollow or solid; observe also the texture, +whether brittle, cartilaginous, fibrous, or fleshy. + +[Illustration: FIG. 459.—Parasol mushroom (_Lepiota procera_), +showing movable annulus: _st_, stipe; _a_, annulus, or ring; _u_, +umbo; _p_, _p_, floccose patches left by volva.] + +[Illustration: FIG. 460.—Chanterelle (_Cantharellus cibarius_), with +infundibuliform pileus and decurrent gills.] + +=373. The pileus, or cap.=—Observe this as to color and surface, +whether dry, or moist and sticky; smooth, or covered with scurf or +scales left by the remains of the volva, as it was stretched and +broken up by the expanding cap (Fig. 459, _p_, _p_). Note also the +size and shape, whether conical, expanded, funnel-shaped (Fig. 460), +or _umbonate_—having a protuberance at the apex (Fig. 459)—or whether +the margin is turned up at the edge (revolute, Fig. 467), or under +(involute, Fig. 459). + +=374. The gills, or laminæ.=—Look at the under surface and notice +whether the gills are broad or narrow, whether they extend straight +from stem to margin, or are rounded at the ends, or curved, toothed, +or lobed in any way. Notice their attachment to the stipe, whether +_free_, not touching it at all; _adnate_, attached squarely to the +stem at their anterior ends; or _decurrent_, running down on the stem +for a greater or less distance (Fig. 460). + +[Illustration: FIGS. 461-463.—Section of a gilled mushroom: 461, +through one side, showing sections of the pendent gills, _g_, _g_ +(slightly magnified); 462, one of the gills more enlarged, showing +the central tissue of the trama, _tr_, and the broad border formed by +the hymenium, _h_; 463, a small section of one side of a gill very +much enlarged, showing the club-shaped basidia, _b_, _b_, standing +at right angles to the surface, bearing each two small branches with +a spore, _s_, _s_, at the end. The sterile paraphyses, _p_, are seen +mixed with the basidia.] + +[Illustration: FIGS. 464, 465.—A tube fungus (_Boletus edulis_): 464, +entire; 465, section, showing position of the tubes.] + +=375. The hymenium.=—Cut a tangential section through one side of +the pileus and sketch the section of the gills as they appear under +a lens, or a low power of the microscope. Notice that the blade +consists of a central portion called the _trama_ (_tr_, Fig. 462) +and a somewhat thickened portion, _h_, constituting the _hymenium_, +or spore-bearing surface. Now examine, under a high power, a small +section from the edge of a gill, including a bit of the trama. +Notice that this last consists of a tissue of mycelial cells (Fig. +463) covered by the hymenium, or spore-bearing membrane, which is +thickly clothed with a layer of elongated, club-shaped cells (_b_, +_b_ and _p_, _p_, Fig. 463) set upon it at right angles to the +surface. Some of these put out from two to four, or in some species +as many as eight, little prongs, each bearing a spore (_s_, _s_, +Fig. 463), while others remain sterile. The spore-bearing cells +are called _basidia_; the sterile ones, _paraphyses_; and the +whole spore-bearing surface together, the _hymenium_, from a Greek +word meaning a membrane. It is from the presence of this expanded +fruiting membrane that the class of mushrooms we are considering gets +its botanical name, _Hymenomycetes_, membrane fungi. The hymenium +is not always borne on gills, but is arranged in various ways which +serve as a convenient basis for distinguishing the different orders. +In the tube fungi, to which the edible boletus belongs (Figs. 464, +465), the basidia are placed along the inside of little tubes that +line the under side of the pileus, giving it the appearance of a +honeycomb. In another order, the porcupine fungi, they are arranged +on the outside of projecting spines or teeth, while in the morelles +they are held in little cups or basins. + +[Illustration: FIG. 466.—Spore print of a gilled mushroom.] + +[Illustration: FIG. 467.—Deadly agaric (_Amanita phalloides_), +showing the broad pendent annulus, _a_, formed by the ruptured veil; +the cup at the base, _c_, and floccose patches on the pileus, left by +the breaking up of the volva.] + +=376. Spore prints.=—When the gills are ripe, they shed their spores +in great abundance. Take up the pileus that was laid on paper, +as directed under Material, on page 323, and examine the print +made by the discharged spores; it will be found to give an exact +representation of the under side of the pileus. + +=377. The spores.=—Notice the color of the spores as shown in the +print. This is a matter of importance in distinguishing gill-bearing +fungi, which are divided into five sections according to the color of +the spores. One source of danger, at least, to mushroom eaters would +be avoided if this difference was always attended to, for the deadly +amanita (_Amanita phalloides_) and the almost equally dangerous fly +mushroom (_A. muscaria_) both have white spores, while the favorite +edible kind (_Agaricus campestris_), though white-gilled when young, +produces dark, purple-brown spores that cannot fail to distinguish it +clearly for any one who will take the trouble to make a print. + +=378. Economic properties.=—Most of the wood-destroying fungi belong +to this and allied orders. They are among the worst enemies the +forester has to deal with (140), and millions of feet of lumber are +destroyed every year by them. + +[Illustration: FIG. 468.—Portion of the root of a maple affected with +rot caused by the mycelium of a fungus that has penetrated to its +interior.] + +Over seven hundred kinds of fungi growing in the United States have +been described as edible, but the evil repute into which the whole +class has been brought by the poisonous qualities of a few species, +and the difficulty, to any but an expert, of distinguishing between +these and the harmless kinds, has caused them to be generally +neglected as articles of diet. While they are pleasant relishes and +furnish an agreeable variety to our daily fare, their food value has +been greatly exaggerated. They contain a large proportion of water, +often over 90 per cent, and the most valued of them, the _Agaricus +campestris_, is about equivalent to cabbage in nutrient properties. + + + Practical Questions + + 1. Why are mushrooms generally grown in cellars? (186, 343.) + + 2. Name any fungi you know of that are good for food or medicine or + any other purpose. + + 3. Name the most dangerous ones you know of. + + 4. Do you find fungi most abundant on young and healthy trees, or + on old, decrepit ones? Account for the difference. (141, 343, 378.) + + 5. Do you ever find them growing on perfectly sound wood anywhere? + + 6. Are they ever beneficial to a tree? (86.) + + 7. Is it wise to leave old, unhealthy trees and decaying trunks in + a timber lot? + + + IV. LICHENS + + MATERIAL.—Specimens can be found almost everywhere, growing on + rocks, walls, logs, stumps, and trees. Some of the more common + kind are: _Parmelia_, recognizable by the shallow spore cups borne + on the upper surface of the thallus; _Cladonia_, by the little + stalked receptacles, like goblets, in which its spores are held; + _Physcia_, by its bright orange color. Where practicable, it is + well to have several different kinds for comparison. Iceland moss + (_Cetraria islandica_) can generally be obtained from the grocers, + and is a good example of an intermediate form between foliaceous + and fruticose lichens. + + If the specimens are very dry, they will be too brittle to handle + conveniently, and should be moistened by soaking a short time in + water. This will render them quite flexible and also bring out the + green color more clearly. + +[Illustration: FIG. 469.—Foliaceous lichens: _A_, _Xanthoria +(Physcia) parietina_; _B_, _Parmelia conspersa_; _a_, spore cups.] + +=379. Examination of a typical specimen.=—The commonest kind of +lichens, and generally the most easily obtained, are those that +grow on rocks and tree trunks in flat, spreading patches. Their +margins are much dented and curled, giving them a somewhat leaflike +appearance, whence they are called “foliaceous” lichens. This broad, +expanded body is the thallus, or vegetative part, as distinguished +from its reproductive part. Examine carefully the thallus of your +specimen. Note the size and shape of the indentations. Is there any +order or regularity about them, such as was observed in the lobing of +leaves? Is there any difference in color between the upper and under +sides? What other differences do you notice? Do you see anything +like hairs, or rootlets, on the under side? Mount one of them in +water and place under the microscope. What does it look like? Compare +with one of the hairs from a leaf of mullein, gromwell, blueweed, or +other hairy plant, with the hypha of a fungus mycelium, and with your +study of the root hair in 67 (_a_). Is it a hair or a root? These +rootlike hairs are called _rhizoids_, and serve to anchor the lichen +to its substratum. Look on the upper side for little cup-shaped or +saucer-shaped receptacles. On what part of the thallus are they +situated? Examine with a lens and see if you can make out what they +contain. These cups are the spore cases. The lichen fungus belongs to +the division of sac fungi, which produce their spores in closed sacs, +or cups. + +[Illustration: FIG. 470.—Portion of the thallus of a lichen, +magnified, showing imprisoned algæ.] + +=380. Structure of the thallus.=—Make a thin section through a +thallus and place under the microscope. Notice the small green bodies +enveloped in the hyphæ of the fungus. Are they most abundant near the +upper or the lower epidermis? Has their green color anything to do +with this, and with the difference in color between the two surfaces +of the thallus? (184.) Do they look like chlorophyll granules? Can +you tell what they are? Compare with your study of the unicellular +algæ (337) and with Fig. 429. Does this throw any light on their real +nature? + +[Illustration: FIG. 471.—Artificial lichen mycelium, _m_, made by +sowing spores of a fungus, _sp_, among alga cells, _a_.] + +=381. The lichen thallus a composite body.=—You will probably have no +difficulty in making out that these small round bodies are green algæ +of some kind, but of what species will depend upon the kind of lichen +with which it is associated. In Cladonia and the bearded lichen +(Fig. 473), it is a protococcus; in other forms, a pleurococcus or a +nostoc—and so on, each species of lichen fungus being specialized to +a certain form of alga. The great botanist, De Bary, showed that it +is even possible to produce a lichen thallus artificially by sowing +the spores of a fungus among the cells of the particular alga with +which it is able to unite. The spores will germinate without the +alga, but soon perish unless they come in contact with the right +one. It is thus made clear that the lichen plant as a whole is a +combination of elements belonging to two distinct orders, the algæ +and fungi, but so closely associated as to constitute practically a +single individual. + +=382. Slavery, or partnership?=—Now, what can be the object of this +peculiar association? Is it a symbiosis, or a case of enslavement? +The fungi, as we know, are all parasites, unable to manufacture +their own food or to exist at all except at the expense of other +organisms, living or dead. But the lichens have refined upon the +gross rapacity of their order, and instead of indiscriminately +destroying the hosts that furnish their nourishment, have used their +victims to better purpose by converting them into contented, well-fed +slaves! The imprisoned algæ perform for them the same service that +the chlorophyll bodies do for the higher plants, and so the lichen +fungi have the advantage of other parasites in getting their food +manufactured at home, so to speak. And while the algæ have to do +double work in order to feed both themselves and their masters, +the fungus, in return, shelters them against cold and drought, and +prolongs their growing period by giving them a more continuous supply +of moisture and food materials, which it draws from the substratum by +means of its rhizoids. In this way both plants are enabled to live in +situations that neither could occupy without the other. + +[Illustration: FIG. 472.—A crustaceous lichen (_Graphis elegans_) +growing on holly: _A_, natural size; _B_, slightly magnified.] + +=383. Reproduction.=—The multiplication of the lichen algæ is +exclusively vegetative. The fungus, on the other hand, reproduces +normally by spores, and the fruiting bodies found on the thallus +originate from the fungus mycelium. + +=384. Classification.=—To be strictly accurate, the two kinds of +vegetable bodies that make up the lichen thallus would probably have +to be classified separately, as algæ or fungi, respectively, but as +fructification is the generally accepted basis of classification, +and the plant body is too intimately permeated with both kinds of +tissue to be divided, each lichen body as a whole is classed with +its particular kind of fungus. The entire group, on account of the +distinctive characters that mark it, is placed in a separate order +of its own. This includes three principal divisions, distributed +according to the shape of the thallus, and its habit of growth: +(1) _Crustaceous_, those that adhere closely to the substratum, as +if glued or inscribed on it; (2) _Foliaceous_, with a broad, more +or less lobed and leaflike thallus that adheres loosely to the +substratum by means of rhizoids springing from its under surface; (3) +_Fruticose_, with branching, stemlike thallus attached at the base +like a regularly rooting plant (Figs. 473, 474). Among these are the +Iceland moss, used as an article of food by man, and the reindeer +moss (_Cladonia rangiferina_), which is the chief sustenance of the +reindeer. + +[Illustration: FIGS. 473, 474.—Fruticose lichens: 473, _Usnea +barbata_, bearded lichen; 474, _Cladonia rangiferina_, reindeer moss: +_A_, sterile; _B_, fruiting portion.] + + + Practical Questions + + 1. Have lichens any economic value? (384.) + + 2. In what way are they most useful? (320.) + + 3. Do you find them, as a general thing, on healthy young trees and + boughs, or on old ones, and those showing signs of decay? + + 4. Do you ever find them growing on trees or other objects in + densely inhabited areas,—cities, large towns, and manufacturing + centers? + + 5. Do they grow more thickly on the shady (northern) side of + rocks, walls, and trees growing in the open, than on the sunny and + (presumably) warmer sides? + + 6. Mention some ways in which a growth of lichens might be + beneficial to a tree. + + 7. In what ways could it be harmful? + + + V. LIVERWORTS + + MATERIAL.—Liverworts can generally be found growing with mosses + in damp, shady places, and are easily recognized by their flat, + spreading habit, which gives them the appearance of green lichens. + _Marchantia polymorpha_ (Fig. 475), one of the largest and best + specimens for study, is common in shady, damp ground throughout + the states. It is diœcious, and specimens bearing both male and + female organs should be provided. _Lunularia_, a smaller species + that can be recognized by the little crescent-shaped receptacles on + some of the divisions of the thallus, is abundant in greenhouses on + the floor, or on the sides of pots and boxes kept in damp places; + but the spore-bearing receptacles are seldom or never present, the + species being an introduced one and possibly rendered sterile by + changed conditions. _Anthoceros_ (Fig. 426) and leafy liverworts, + such as that shown in Fig. 484, also make good examples for study. + + EXPERIMENT 97. WHY ARE THE UPPER AND UNDER SIDES OF A LIVERWORT + DIFFERENT?—Plant a growing branch of marchantia, or of any flat, + spreading liverwort, in moist earth so that the upper side will lie + next the soil, and watch for a week or two, noting the changes that + take place. What would you infer from these as to the cause of any + differences that may have been observed between the two surfaces? + +=385. Examination of a typical liverwort=—The thallus.—The broad, +flat, branching organ that forms the body of the plant is the +thallus. Examine the end of each branch; what do you find there? Are +the two forks into which the apex of the branches divides equal or +unequal? Compare the growing end with the distal one; does it proceed +from a true root? Notice that as the lower end dies, the growing +branches go on increasing and reproducing the thallus. + +[Illustration: FIGS. 475, 476.—Umbrella liverwort (_Marchantia +polymorpha_): 475, portion of a female thallus about natural size, +showing dichotomous branching; _f_, _f_, archegonial or female +receptacles; _r_, rhizoids; 476, portion of a male thallus bearing an +antheridial disk or receptacle, _d_, and gemmæ, _g_, _g_.] + +[Illustration: FIG. 477.—A portion of the upper epidermis of +marchantia, magnified, showing rhomboidal plates with a stoma in +each.] + +Do you find anything like a midrib? If so, trace it through the +branches and body of the thallus; where does it end? Does it seem +to be formed like the midrib of a leaf? Hold a piece of the thallus +up to the light and see if you can detect any veins. Is it of the +same color in all parts, and if there is a difference, can you give +a reason for it? Examine the upper surface with a lens. Peel off a +piece of the epidermis, place it under a low power of the microscope, +or between two moistened bits of glass, and hold up to the light, +keeping the upper surface toward you; what is its appearance? +Observe a tiny dot near the center of the rhomboidal areas into which +the epidermis is divided and compare it with your drawings of stomata +(181, 183). What would you judge that these dots are for? While +differing in structure from the stomata of leaves, they serve the +same purposes and may be regarded a more rudimentary form of the same +organ. + +=386. Rhizoids.=—Wash the dirt from the under side of a thallus and +examine with a lens; how does it differ from the upper surface? Do +you see anything like roots? Place one in a drop of water under the +microscope. Compare with similar organs found on the lichen (379). +What are they? Would rhizoids be of any use on the upper side? +stomata on the under side? + +=387. Gemmæ.=—Look along the upper surface for little saucer-shaped +(in lunularia, crescent-shaped) cupules (_g_, _g_, Fig. 476). Notice +their shape and position, whether on a midrib or near the margin. +Examine the contents with a lens and see if you can tell what they +are. These little bodies, called _gemmæ_, are of the nature of +buds, by which the plant propagates itself vegetatively somewhat +as the onion and the tiger lily do by means of bulblets. Sow some +of the gemmæ on moist sand, cover them with a tumbler to prevent +evaporation, and watch them develop the thalloid structure. + +=388. The fruiting receptacles.=—Procure, if possible, thalli with +upright pedicels bearing flattened enlargements at the top (Figs. +475, 476). These are thallus branches modified into receptacles +containing the reproductive organs, which, in marchantia, are +diœcious, the two kinds growing on separate thalli. Notice their +difference in shape, one kind being slightly lobed or scalloped, the +other rayed like the spokes of a wheel. The first kind are known as +_antheridial_, or male, receptacles; the second as _archegonial_, or +female. + +=389. The antheridia.=—Examine one of the male receptacles on +both surfaces and in vertical section. Notice the tiny egg-shaped +bodies sunk in little cavities between the lobes just under the +upper epidermis (Fig. 478). These are antheridia. When mature, they +rupture at the apex, and multitudes of extremely small bodies, called +_antherozoids_, or _spermatozoids_, are discharged from them. + +[Illustration: FIG. 478.—Longitudinal section of a male receptacle of +marchantia polymorpha, magnified: _a_, antheridia; _t_, thallus; _s_, +ventral scales; _r_, rhizoids.] + +[Illustration: FIG. 479.—Under side of an archegonial receptacle +enlarged. The archegonia are borne among the hairs on the under +surface, which is presented to view in the figure; _f_, a spore case.] + +=390. Archegonia.=—Next examine one of the female receptacles. Look +on the under surface, between the narrow divisions of the receptacle, +for radiating rows of flask-shaped bodies with their necks turned +downward, and all surrounded by a toothed sheath or involucre +(Fig. 479). These bodies are the archegonia, or female organs, and +correspond, loosely speaking, to the ovaries of flowering plants. If +the receptacle is a mature one, the archegonia will be replaced by +the ripe spore cases (_sporangia_), as at _f_, Fig. 479. + +Make enlarged drawings of the upper surface of a male and a female +receptacle, and of a vertical section of each, passing through +an antheridium in the male, and an archegonial row in the female +receptacle. Label the parts observed in each. + +=391. Minute study of an archegonium.=—Place under the microscope +a very thin, longitudinal section through a ray of a receptacle +containing a young archegonium, and observe that the latter consists +of a lower portion, the _venter_, _v_, Fig. 480, and an upper part, +the neck, which is perforated by the _neck canal_, _ca_. The venter +contains the _egg cell_, _o_, and the ventral canal cell, _vc_. The +neck canal is filled with small cells which, at maturity, dissolve +into a mucilaginous substance that swells on being wet and discharges +itself through the top of the neck, leaving an open passage to the +venter, where the egg cell is ready to be fertilized. + +[Illustration: FIGS. 480, 481.—480, young archegonium of M. +polymorpha; _v_, ventral portion; _o_, egg cell; _vc_, ventral canal +and cells; _ca_, neck canal with cells; 481, the same ready for +fertilization after discharge of the mucilaginous fluid.] + +Make a drawing of the section as seen under the microscope, labeling +all the parts. + +=392. Fertilization.=—In the liverworts, and in cryptogams generally, +this process has to take place under water, as the antherozoids are +motile only in a liquid, but the amount required is so small that a +few drops of rain or dew will enable them to make their journey to +the archegonium. The mucilaginous substances discharged from the neck +canal attract them to the mouth of the opening, one or more of them +penetrates to the egg cell, and fertilization is accomplished. Do you +see any analogies between this and the same function among flowering +plants? (250, 251.) + +=393. The spore case.=—After fertilization the egg becomes an +_oöspore_, capable of producing a new plant. Instead, however, of +separating from the mother plant and giving rise to an independent +growth, it germinates within the archegonium and produces there a +small, stalked body, called a _sporogonium_, or _sporophyte_, which +at length ripens into a spore case, as shown at _f_, Fig. 479. At +maturity this capsule-like sporophyte ruptures at the apex, and +discharges a mass of spores, mingled with elongated filaments +called _elators_, which, by their elastic movements, assist in +disseminating the spores. These latter, on germinating, produce, +not a simple sporophyte like that which bore them, but the thallus +of the liverwort with all its complicated arrangement of antheridia +and archegonia and vegetative organs that seem to foreshadow, by the +analogies they suggest, the coming of the higher plants. + +=394. Sexual and asexual reproduction.=—We find here a very marked +change from the simple reproductive processes observed in the algæ +and fungi. In the forms thus far considered, this function was +carried on mainly by simple vegetative fission or budding, with a +more or less irregular intervention of resting spores. If only one +kind of spore is concerned, reproduction is said to be _asexual_. +When two different kinds of cells, the egg and sperm cell, unite to +form an oöspore, as in the liverworts, reproduction is said to be +_sexual_. While sexual reproduction takes place to some extent among +both algæ and fungi, the prevailing method among thallophytes is +asexual, and may be carried on in three different ways: by fission +(and budding), by resting spores, and by conjugation. + +Representing the plant body by _A_ and the resting spores by _a_, +the primitive asexual processes may be expressed to the eye by the +accompanying formulas:— + + (1) Fission and budding: _A_ → _A_ → _A_ → _A_ → + (2) Resting spores: _A a_ → _A a_ → _A a_ → + (3) Conjugation: _A_ + _A_ → _a_ → _A_ + _A_ → _a_ → + +In (3), as was seen in the conjugating cells of the spirogyra (342), +the method is a little more complicated, showing an approach toward +the sexual process. In each of these cases, however, there is only +one kind of cell concerned, while in the liverworts there are not +only different kinds, technically known as _gametes_, but specialized +organs, archegonia and antheridia, for producing them. The thallus +body bearing these organs is termed the _gametophyte_, because it +bears the gametes, or sexual organs,—the suffix _phyte_ meaning a +plant; for example, _epiphyte_, on or upon plants; _spermophyte_, +or _spermatophyte_, seed plant; _sporophyte_, spore plant. The +_sporophyte_, produced within the archegonium, bears simple nonsexual +spores that are capable of germinating independently. Structurally it +is a separate, individual organism, though it does not appear as such +in this class, but lives inclosed in the archegonium, as a parasite +on the mother plant. + +=395. Alternation of generations.=—If we represent the sporophyte +by _S_, the thallus, or gametophyte, by _G_, the female gamete, or +egg cell, by _fg_, the antherozoids (male gametes) by _mg_, the +fertilized egg cell, or oöspore, resulting from their union by _oös_, +and the asexual spores discharged from the sporophyte by _o_, this +complicated mode of reproduction may be expressed diagrammatically as +follows:— + + _fg_ _fg_ + ╱ ╲ ╱ ╲ + _G_ _oös_→_s_→_o_→_G_ _oös_→_s_→_o_→_G_→etc. + ╲ ╱ ╲ ╱ + _mg_ _mg_ + +A glance at the diagram will show a continual interchange of the +sexual and asexual modes of reproduction, in which each generation +gives rise to its _opposite_, the asexual sporophyte producing +the sexual gametophyte, and this in turn, through its gametes, +giving rise to the asexual sporophyte. This regular recurrence +in genealogical succession of two differing forms is what is +meant by the expression “alternation of generations.” Analogous +processes occur also among some of the thallophytes, but as there +is no well-defined differentiation of sporophyte and gametophyte, +alternation proper may be regarded as beginning with the bryophytes. +The subject is a complicated one and somewhat difficult to grasp, +but it is important to form a correct idea of it and to fix clearly +in mind the different modes of reproduction as we proceed from the +lower to the higher forms of vegetation, since in this way alone can +their biological relationships and their order of succession in the +evolutionary scale be made intelligible. + + + VI. MOSSES + + MATERIAL.—One of the most widely distributed of mosses is the + Sphagnum, or peat moss, so generally used by florists in packing + plants for shipment, and it can be obtained from them at almost all + times. It is rather difficult, however, to find specimens with the + fruiting organs, since they are rarely to be met with except in + late autumn or early spring. Other common forms are _Polytrichum_, + _Funaria_, and _Mnium_, any of which will meet all essential + conditions of the study outlined in the text. + +[Illustration: FIGS. 482, 483.—Protonema of a moss: 482, germinating +spore; 483, protonema; _kn_, buds; _r_, rhizoids; _s_, spore.] + +=396. The protonema or thallus stage.=—In mosses the sexual, or +gametophyte generation differs from that of liverworts in undergoing +two phases. The germinating cells of the sporophyte do not develop +immediately into the leafy stem, which is the typical gametophyte +of true mosses, but produce first a filamentous, creeping structure +called the _protonema_ (Fig. 483), that spreads over the ground +and forms the tangled green felt usually observed where mosses are +growing. Place a few of these filaments on a slide in water, and +examine under the microscope. Do they remind you of any of the +forms of algæ? Look near the base of the branches for knots or +enlargements, like those seen at _kn_, Fig. 483. These are buds +from which the leafy moss stems will develop. Do they correspond +to anything observed among the thallophytes? Notice the rootlike +filaments that extend under ground; how do they differ from the ones +above ground? Why are they colorless? How do you know that they are +not true roots? [67 (_a_), 379.] Sketch one of each kind of filament +sufficiently enlarged to show the cells composing it. + +A protonema that arises directly from the spore is said to be +_primary_, while those which sometimes spring from rhizoids above +ground, or from stems or leaves, are _secondary_. The fact that a +protonema can bud from parts of the fruiting stems shows that the two +do not belong to different generations, but are merely successive +stages of a single generation, and both together compose the +gametophyte. + +=397. The leafy stage.=—In their fully developed state the true +mosses show a marked advance in organization over the liverworts. +There is a distinct differentiation of the growing axis into stem +and leaves, though no true roots are formed. The leaves are arranged +spirally, on upright stems, while in the liverworts the vegetative +body is either a flat, spreading thallus, or the leaves are arranged +horizontally on opposite sides of a prostrate, or more or less +inclined, axis. Sometimes a second set occurs, on the upper side of +the axis, but in this case the leaves are usually much smaller and +inclined to the horizontal arrangement, as shown in Fig. 484. + +[Illustration: FIG. 484.—Scapania, a liverwort with leafy thallus, +approaching the form of mosses and lycopodiums. (_From_ COULTER’S +“Plant Structures.”)] + +[Illustration: FIG. 485.—Fruiting receptacle of a moss (_Phascum +cuspidatum_), bearing both antheridia, _an_, and archegonia, _ar_, at +the bifurcated apex; _b_, leaves; _p_, paraphyses.] + +[Illustration: FIG. 486.—Fruiting stem of a moss (_Polytrichum +commune_) with ripe capsules: _s_, seta, or footstalk; _c_, capsule +with calyptra; _f_, capsule after the calyptra has fallen away; _d_, +operculum, or lid.] + +=398. The reproductive organs.=—The antheridia and archegonia are +borne in groups at the end either of the main axes, or of lateral +branches (Figs. 485, 486), but as a rule only one archegonium is +fertilized, so the mature sporogonia are solitary. The plants may be +either diœcious or monœcious, as in Fig. 485; and in the latter case, +the reproductive organs may be borne on the same, or on different, +receptacles. The antheridia and the archegonia are both mixed with +club-shaped hairs called paraphyses (Fig. 485). + +=399. The sporophyte.=—An examination of the fruiting capsule of any +of the true mosses will show that it consists of a long footstalk, +the _seta_, _s_, Fig. 486, bearing a capsule, or ripened sporogonium, +_f_, which is at first surmounted by a cap or hood, known as the +_calyptra_, _c_. The hood represents the excessively developed and +often highly specialized wall of the archegonium. It falls away at +maturity, and the spores are discharged through an opening made by +the removal of the _operculum_, or lid, _d_. The spores and the +capsule are both developed from the fertilized egg (oöspore), within +the archegonium, in much the same manner as in the liverworts, and +together constitute the sporophyte, or asexual generation. It never +leads a completely independent existence, but remains a partial +parasite on the mother plant, though the lower part of the young +sporogonium is usually provided with stomata and chlorophyll so +that it is capable of manufacturing food. In this respect it shows +a distinct advance on the corresponding phase of the liverworts—if +we except the single genus _Anthoceros_, which alone among the +liverworts has the cells of the sporogonium provided with chlorophyll. + +=400. Alternation of generations.=—The process of reproduction +in mosses is so closely similar to that of liverworts that it is +unnecessary to repeat the details. There are some minor variations, +but in all essentials the processes are the same and may be +represented to the eye by the same formula. + +=401. Relative position of mosses and liverworts in the line of +evolution.=—Though mosses, as a rule, show a higher degree of +organization than liverworts, in both generations, their development +has been _away_ from the general course of evolution followed by +the higher plants. This, as will be seen later, tends towards a +decreasing complexity of the gametophyte with increasing complexity +of the sporophyte, while the mosses show increasing complexity of +_both_. Like the order of birds in the animal kingdom, they form a +highly specialized and somewhat isolated group. While they may be +regarded as descendants from a common ancestral stock with the ferns +and club mosses, they have been switched off, so to speak, on a +side track of the great evolutionary trunk line, and their advance +on this side track has carried them to a point more remote from the +course along which the higher forms of plant life have traveled than +the distant junction at which they branched off from their less +progressive kindred, the humble liverworts. + + + VII. FERN PLANTS + + MATERIAL.—Any kind of fern in the fruiting stage. Several different + varieties should be cultivated in the schoolroom for observation. + While gathering specimens, look along the ground under the fronds, + or in greenhouses where ferns are cultivated, among the pots and + on the floor, for a small, heart-shaped body like that represented + in Figs. 501, 502, called a _prothallium_. It is found only in + moist and shady places, and care should be taken in collecting + specimens, as in their early stages the prothallia bear a strong + resemblance to certain liverworts found in the same situations. The + best way is for each class to raise its own specimens by scattering + the spores of a fern in a glass jar, on the bottom of which is a + bed of moist sand or blotting paper. Cover the jar loosely with a + sheet of glass and keep it moist and warm, and not in too bright a + light. Spores of the sensitive ferns (_Onoclea_) will germinate in + from two to ten days, according to the temperature. Those of the + royal fern (_Osmunda_) germinate promptly if sown as soon as ripe, + but if kept even for a few weeks are apt to lose their vitality. + The spores of sensitive fern can be kept for six months or longer, + while those of the bracken (_Pteris_) and various other species + require a rest before germinating, so that in these cases it is + better to use spores of the previous season. + +[Illustration: FIGS. 487-491.—A fern plant: 487, fronds and +rootstock; 488, fertile pinna: _s_, _s_, sori; 489, cross section of +a stipe, showing ends of the fibrovascular bundles; 490, a cluster of +sporangia, magnified; 491, a single sporangium still more magnified, +shedding its spores.] + +=402. Study of a typical fern.=—Observe the size and general outline +of the fronds, and note whether those of the same plant are all +alike, or if they differ in any way, and how. Observe the shape +and texture of the divisions or pinnæ composing the frond, their +mode of attachment to the rachis, and whether they are simple, or +notched, or branched in any way. Hold a pinna up to the light and +notice the veining. Is it like any of the kinds described in 171, +172? In what respect is it different? This forked venation is a very +general characteristic of ferns. When the forks do not reticulate +or intercross, the veins are said to be free; are they free in your +specimen, or reticulated? Make a sketch, labeling the primary +branches of the frond, _pinnæ_ (sing., _pinna_), the secondary ones, +if any, _pinnules_, and the common stalk that supports them, _stipe_. +Note the color, texture, and surface of the stipe. If any appendages +are present, such as hairs, chaff, or scales (in Pteris, nectar +glands), notice whether they are equally distributed. If not, where +are they most abundant? + +Examine the mode of attachment of the stipes to their underground +axis. Break one away and examine the scar. Compare with your drawings +of leaf scars and with Fig. 105. Do the stipes grow from a root or a +rhizome? How do you know? Do you find any remains of leafstalks of +previous years? How does the rootstock increase in length? Measure +some of the internodes; how much did it increase each year? Cut a +cross section and look for the ends of the fibrovascular bundles. +Trace their course through several internodes. Do they run straight, +or do they turn or bend in any way at the nodes? If so, where do they +go? Do you see anything like roots? Where do they originate? Put one +of them under the microscope and find out whether they are roots or +hairs. + +True roots are first developed in the pteridophytes. Since those of +the fern spring from an underground stem, to what class of roots do +they belong? (83.) + +=403. Minute study of a fern stem.=—Place a very thin section of +a fern rhizoma, or of the stipe of a frond, under the microscope. +Except in very young stems the vascular bundles are arranged in a +ring, or sometimes in two or more rings (Fig. 492), with plates of +strengthening tissue, _l_, _l_, between the inner and outer rings. +Notice the inner epidermal layer of hard brown tissue, and within +that, the soft parenchyma, which fills the rest of the interior. Test +it with iodine and observe how rich in starch it is. If the section +of a petiole is under observation, the details will be somewhat +different; would you expect to find as much starch in the stipe as in +the rootstock? Why, or why not? + +Make a longitudinal section of a rhizome through the point where +a leafstalk is attached and trace the course of the bundles. This +will be facilitated if the specimen has stood in eosin solution a +few hours. Make enlarged drawings of both sections, labeling all the +parts. + +[Illustration: FIG. 492.—Diagram of a cross section through the +stem of a fern (_Pteris_): _s_, _s_, _s_, rings of fibrovascular +bundles; _l_, _l_, plates of strengthening tissue, with a ring of +fibrovascular bundles between them; _lp_, zone of strengthening +fibers; _r_, cortex; _e_, epidermis.] + +[Illustration: FIGS. 493-494.—Parts of fertile pinnæ: 493, of +_polypodium_, enlarged, showing the sori without indusium; 494, of +_pellea_, showing indusium formed by the revolute margin.] + +Clearly differentiated conducting bundles occur in the mosses, +but they are of much simpler structure than in the pteridophytes, +consisting usually of a single central strand, and are found +more frequently in the leaves than in the stems. A true vascular +structure appears first in the pteridophytes, whence these plants are +distinguished as _vascular cryptogams_. + +=404. Fructification.=—Examine the back of a fruiting frond; what +do you find there? These dots are the _sori_ (sing., _sorus_), or +spore clusters, and the fronds or pinnæ bearing them are said to be +_fertile_. Are there any differences of size, shape, etc., between +the fertile and the sterile fronds of your specimen? between the +fertile and the sterile pinnæ? On what part of the frond are the +fertile pinnæ borne? Notice the shape and position of the sori, +and their relation to the veins, whether borne at the tips, in the +forks, on the upper side (toward the margin), or the lower (toward +the midrib). Look for a delicate membrane (_indusium_) covering the +sori, and observe its shape and mode of attachment. If the specimen +under examination is a polypodium, there will be no indusium; if a +maidenhair, or a bracken, it will be formed of the revolute margin +of the pinna. In lady fern and Christmas fern (_Aspidium_), the sori +frequently become confluent, that is, so close together as to appear +like a solid mass. Sketch a fertile pinna as it appears under the +lens, bringing out all the points noted. + +[Illustration: FIGS. 495-496.—Christmas fern (_Aspidium_): 495, part +of a fertile frond, natural size; 496, a pinna enlarged, showing the +sori confluent under the peltate indusia.] + +[Illustration: FIGS. 497-500.—Spores of pteridophytes, magnified: +497, a fern spore; 498, 499, two views of a spore of a club moss; +500, spore of a common horsetail (_Equisetum arveuse_).] + +=405. The spore cases.=—Look under the indusium at the cluster +of little stalked circular appendages (Fig. 490). These are the +_sporangia_, or spore cases, in which the reproductive bodies are +borne. Place one of them under the microscope, and it will be found +to consist of a little stalked circular body like a tennis racket +(Fig. 491), surrounded by a jointed ring called the _annulus_. Watch +a few moments and see if you can find out the use of the annulus. If +not, warm the slide and you will probably see the ring straighten +itself with a sudden jerk, rupturing the wall of the sporangium and +discharging the spores with considerable force. If this does not +happen, add a drop of strong glycerine to a specimen mounted in +water; the rupture will be apt to follow quickly. What causes it, in +either case? [56, (1); Exp. 19.] + +=406. The sporophyte.=—The spores found in such abundance on the +fertile pinnæ; are all alike, and each one is capable of germinating +and continuing the work of reproduction as effectually as the sexual +spores of the bryophytes. The fertile frond, or part of a frond, on +which they are borne is called a _sporophyll_ (spore-bearing leaf), +and the entire plant is the _sporophyte_, which, with its crop of +spores, makes up one generation. + +It is important to observe that in the ferns and in all pteridophytes +the sporophyte is the conspicuous and highly organized body that +is commonly recognized as the normal growing plant; while with the +bryophytes just the reverse holds true,—the sexual generation, +or gametophyte, represents the normal plant structure, while the +sporophyte is an insignificant appendage which never attains an +independent existence. Broadly speaking, in bryophytes, it is a spore +fruit; in the pteridophytes and spermatophytes a highly developed +plant. + +[Illustration: FIGS. 501, 502.—Prothallium of a common fern +(_Aspidium_): 501, under surface, showing rhizoids, _rh_, antheridia, +_an_, and archegonia, _ar_; 502, under surface of an older +gametophyte, showing rhizoids, _rh_, young sporophyte, with root, +_w_, and leaf, _b_.] + +=407. The gametophyte.=—When one of these asexual spores germinates, +it produces, not a fern plant like the one that bore it, but a small, +heart-shaped body like that shown in Fig. 501. Examine one of these +bodies carefully with a lens. Observe that there are no veins nor +fibrovascular bundles, and the whole body of the plant seems to +consist of one uniform tissue. Compare it with the forked apex of +a branching thallus of a liverwort. Do you perceive any points of +similarity? The two are, in fact, morphologically the same. This +heart-shaped body is called a _prothallium_, and is the gametophyte +of the fern. It may be of different shapes, and in some species is +branching and filamentous, like the protonema of a moss. Generally, +however, it is flat and more or less two-lobed, as shown in Fig. +501. It is small and inconspicuous and very short-lived, being of +importance only in connection with the work of reproduction. + +Look with your lens for a cluster of small, bottle-shaped bodies +just below the deep cleft in the heart. If you cannot make out what +they are, put a thin section through a part of the prothallium +containing one under the microscope, and you will see that they are +the archegonia. Lower down among the rhizoids, near the pointed base, +will be found the antheridia. In some species the prothalli are +diœcious, one kind bearing antheridia, the other archegonia, but this +is rare among the true ferns. + +[Illustration: FIG. 503.—Young archegonium of a fern, magnified: _K_, +neck canal cell; _K′_, ventral canal cell: _O_, egg cell.] + +=408. Fertilization.=—This process is the same in all essentials as +in the bryophytes. As in other cryptogams, it can take place only +under water,—a circumstance which points to an aquatic origin for +this sub-kingdom, and through them to the entire flora of the globe. +The archegonia differ somewhat in shape from those of the liverworts +and mosses, but a section under the microscope will show that they +consist of essentially the same parts. On account of the similarity +of these organs, the pteridophytes and bryophytes are often classed +together as _Archegoniates_. + +=409. Alternation of generations.=—Among the section of ferns that +we have been considering, the order of alternation corresponds in +all essentials to that prevailing among the bryophytes, and may +be represented by the same formula. The chief difference is in the +relatively much greater importance of the sporophyte, which may be +expressed by putting it first:— + + _fg_ _fg_ + ╱ ╲ ╱ ╲ + _S_→_o_→_G_ _oös_→_S_→_o_→_G_ _oös_→_S_→_o_→_G_ etc. + ╲ ╱ ╲ ╱ + _mg_ _mg_ + +But some of the pteridophytes—of which the Selaginella offers a +conspicuous example—have differentiated their asexual spores (_o_ +of the formula) into two kinds, large and small, known respectively +as _megaspores_ and _microspores_. The prothallia developed by the +former bear archegonia containing female gametes only; those by the +latter, antheridia containing male gametes—while in the diœcious +bryophytes, the archegonial and antheridial thalli are produced by +spores of the same kind. + +[Illustration: FIGS. 504.-508.—A kind of pteridophyte (_Selaginella +martensii_) with its organs of fructification: 504, a fruiting +branch; 505, a microsporophyll with a microsporangium, showing +microspores through a rupture in the wall; 506, a megasporophyll +with a megasporangium; 507, megaspores; 508, microspores. (_From_ +COULTER’S “Plant Structures.”)] + +The differentiation of the asexual spores in the higher pteridophytes +gives rise to corresponding changes in the sporangia that bear +them, and even in the sporophylls themselves, one kind bearing +microsporangia only, the other megasporangia. In this way the +differentiation of sex is pushed back, step by step, until it +virtually begins with the sporophyte, or asexual generation. + +Using the same terms as before, and representing the microspores +by the abbreviation _mo_, the megaspores by _Mo_, the archegonial +gametophyte by _arG_, the antheridial by _anG_, the formula may be +modified to express this more complicated process of alternation, as +follows:— + + _Mo_→_arG_→_fg_ _Mo_→_arG_→_fg_ + ╱ ╲ ╱ ╲ + _s_ _oös_→_S_ _oös_→_S_ etc. + ╲ ╱ ╲ ╱ + _mo_→_anG_→_mg_ _mo_→_anG_→_mg_ + + +Comparing this formula with the preceding, it will be seen that the +increased complexity affects the sporophyte at the expense of the +gametophyte, which has now become a mere dependent on the former. + +=410. Advantages of alternation.=—This roundabout mode of +reproduction would hardly have been developed unless it had been of +some benefit to the plants in which it occurs. The chief advantage +seems to be in more rapid multiplication and consequently better +chance to propagate the species, as compared with the slow process +of sexual reproduction were the plant confined to that method alone. +Only one plant is produced by each oöspore, and if this were a +gametophyte with its limited number of archegonia, multiplication +would be slow; but the sporophyte with its millions of spores, +each capable of producing a new individual, enables the species +to multiply indefinitely. At the same time the interposition of a +gametophyte, or sexual generation, secures the introduction of a new +strain with effects analogous to those of cross fertilization. + +[Illustration: FIG. 509.—Part of the fruiting stem of a scouring +rush, _Equisetum limosum_, showing the cone-like spore cluster. +(_After_ GRAY.)] + +=411. Classification of pteridophytes.=—In our study of this group, +the ferns have been taken as the type because they are the most +familiar and most widely distributed of all the vascular cryptogams. +But while they exceed in numbers, both of individuals and species, +all the other orders combined, they form only one division of three +great groups that make up the class Pteridophyta. These groups are: +(1) ferns, under which are included, besides the true ferns, two +widely differing orders, with the grape ferns and adder’s-tongue in +one, and the water ferns in the other; (2) the club mosses, embracing +the two subdivisions of _Lycopodium_ and _Selaginella_; (3) the +horsetail family, including horsetails and scouring rushes. Orders +(2) and (3) are grouped together as cone-bearing (strobilaceous) +pteridophytes, because their sporangia are clustered in oblong heads, +or _strobiles_ (Fig. 509), somewhat like the cones of the pine. The +orders of pteridophytes differ greatly among themselves, but agree +in possessing certain characteristics that point to their derivation +from a common ancestry. + +=412. Distinction between pteridophytes and bryophytes.=—In passing +from the Thallophytes and Bryophytes to the vascular cryptogams, we +cross the widest chasm in the vegetable kingdom—a gap relatively as +great as that between vertebrates and invertebrates among animals. +The most important modifications that discriminate the two groups +are: (1) the presence in Pteridophytes of a highly organized vascular +system accompanied by a well-marked differentiation of the plant body +into root and stem; (2) increased importance and complexity of the +sporophyte with proportionate diminution of the gametophyte. + +While vessels for conducting water occur in some of the bryophytes +(403), a well-defined vascular system and true roots are met with +first in the Pteridophytes. The change in the relative importance +of sporophyte and gametophyte is so marked that in Selaginella, the +genus which approaches nearest in structure to the seed-bearing +plants, the suppression of the gametophyte has proceeded so far that +it never leads an independent existence at all and is difficult even +to recognize as a distinct individual. + + + Practical Questions + + 1. Have ferns any economic use—that is, are they good for food, + medicines, etc.? + + 2. What is their chief value? + + 3. Under what ecological conditions do they grow? + + 4. Are they often attacked by insects, or by blights and disease of + any kind? + + 5. Of what advantage is it to ferns to have their stems + underground, in the form of rootstocks? (321.) + + 6. What causes the young frond of ferns to unroll? (54, 98.) + + 7. Name the ferns indigenous to your neighborhood. + + 8. Which of these are most ornamental, and to what peculiarities of + structure do they owe that quality? + + 9. Are cultivated ferns usually raised from the spores or in some + other way? Why? + + 10. After the great eruption of Krakatoa in 1883, by which the + vegetation of the island was completely destroyed, ferns were the + first plants to reappear. Explain why. (19; Exp. 17.) + + + VIII. THE RELATION BETWEEN CRYPTOGAMS AND SEED PLANTS + +=413. No break in the chain of life.=—The great gap that was once +supposed to exist between the cryptogams and phanerogams has been +bridged over by the discovery of analogies in the reproductive +processes of the two groups that connect them together as successive +links in one continuous chain of vegetable life. It is therefore very +important to have a clear understanding of the nature and meaning of +these processes, for the chief turning points in the life history of +the different groups of plants are connected with them, their natural +relationships to each other, and their distribution according to +their respective places in the evolutionary scale, being determined +largely by a comparison of their modes of continuing the life of the +group. + +=414. Alternation of generations in seed plants.=—This process, so +conspicuous among Bryophytes and Pteridophytes, and not unknown +among Thallophytes, is universal among seed plants (Spermatophytes) +also, though in so masked a form that it is not easy to recognize +without a more detailed study than would be practicable within the +limits of a book like this. Briefly, we may say that the stamens of +spermatophytes, and the pistils, or rather the carpels, which we +have seen to be transformed leaves (298), represent the sporophylls +(406) of the higher pteridophytes. The pollen sacs and ovules are +sporangia, bearing microspores and megaspores (409), represented +respectively by the pollen grains in the anther and the embryo sac +in the ovule. These go through a series of microscopic changes in +the body of the ovule analogous to the production of the oöspore +in the archegonia of ferns and liverworts, but the process is so +obscure that to an ordinary observer the pollen grains and the ovule +appear to be the real gametes, and were long supposed to be such. +The fertilized germ cell in the embryo sac (251) corresponds to +an oöspore; the embryo sac with the endosperm found in all seeds +(previous to its absorption by the cotyledons) is a rudimentary +gametophyte; and the embryo in the matured seed is the undeveloped +sporophyte, destined, after germination and further growth, to +produce a new generation with its recurrent cycle of alternating +phases. + +[Illustration: FIG. 510.—Diagrammatic section through the ovule of a +gymnosperm belonging to the spruce family: _i_, integument covering +the ovule; _e_, endosperm (corresponding to female gametophyte), +which fills the embryo sac, containing two archegonia, _a_; _o_, egg +cell; _p_, pollen grains; _t_, pollen tubes entering the neck, _c_, +of the archegonia.] + +In the gymnosperms,—pines, yews, cycads, etc.,—which represent the +most ancient and primitive type of existing seed-bearing plants, +the similarity of these processes to those of certain of the +pteridophytes is very striking, and it was through the study of +these that the sequences of the process were traced in the much +more obscure form in which they occur among the angiosperms. From +the endosperm in the seeds of gymnosperms archegonia were found to +be developed (Fig. 510) in much the same way as in Selaginella, +from the prothallium, thus showing the endosperm to be a modified +and greatly reduced gametophyte. In some cases, it has even been +found to protrude a little way out of the embryo sac and to take +on a slightly greenish tinge—another reminiscence of its origin. +Fertilization, too, takes place in precisely the same manner as in +the pteridophytes, except that in all but the ginkgo and the cycads, +the fertilizing cells in the pollen grains are non-motile, and find +their way to the ovule by growing down into the embryo sac with the +pollen tube, instead of swimming to it—an adaptation probably brought +about in response to changed condition during the course of evolution +from aquatic to terrestrial life. + +The analogies between the sequence of alternations in the two classes +will be made clearer by a comparison of the accompanying diagrams. +The corresponding terms applied to the various organs stand in +the same vertical row. Diagram (1) shows the process as it takes +place in the more highly developed Pteridophytes; diagram (2) the +corresponding phases in angiosperms. + + + PTERIDOPHYTES + + _mospl_→_mic_→_mo_→_anG_→_ant_→_mg_→ + ╱ ╲ + (1) _S_ _öos_→_S_ + ╲ ╱ + _Mospl_→_Mgc_→_Mo_→_arG_→_arc_→_fg_→ + +_mospl_, microsporophyll; _mic_, microsporangium; _mo_, microspores; +_anG_, male gametophyte; _ant_, antheridia; _mg_, antherozoids. The +letters in the lower line stand for the corresponding female organs. + + + SPERMATOPHYTES + + _st_→_an_→_pol_→_fc_→ _not_ →_gc_→ + ╱ _developed_ ╲ + (2) _S_ _öos_→_S_ + ╲ _developed_ ╱ + _p_ →_ov_→_em_→_end_→ _only in_ →_ec_→ + _gymnosperms_ + +_st_, stamen; _an_, anther; _pol_, pollen; _fc_, food cells in pollen +grain; _gc_, generative cell; _p_, pistil; _ov_, ovules; _em_, embryo +sac; _end_, endosperm; _ec_, egg cell. + + +=415. Disappearance of the gametophyte.=—The seed is a comparatively +recent development in plant evolution. It has no counterpart anywhere +among the cryptogams, but is strictly characteristic of the three +great orders of Spermophytes: Monocotyl, Dicotyl, and Gymnosperms, +which compose the greater part of the vegetation of the globe. +Structurally, it is a matured sporangium containing a rudimentary +sporophyte (the embryo), and a reduced gametophyte (the embryo sac), +which, under the form of endosperm, has dwindled to an insignificance +that makes it difficult to recognize it as a phase in an alternation +of generations. + +=416. Significance of the sporophyte.=—The gametophyte is obviously a +more ancient and primitive structure than the sporophyte, which first +becomes prominent in the ferns and their allies. The sudden and +violent break in the succession of vegetable life that accompanies +the appearance of the pteridophytes (412) is probably to be explained +by the development of a land flora and the necessity of adaptation to +life in a new medium. The fact that no living cell, whether vegetable +or animal, can absorb nourishment except in a liquid form, seems to +point to an aquatic origin more or less remote for all life. This +inference is further strengthened, in the case of plants, by the +fact that even in so highly organized a group as the pteridophytes, +fertilization cannot take place except in water. Such a requirement +would manifestly be a great disadvantage to land plants, and one of +the first steps in response to the demands of a new habitat would be +to get rid, as far as possible, of the primitive gametophyte with +its outgrown adaptations to a liquid medium, and to transfer the +greater part of the work of reproduction to the asexual generation, +in which the problem of fertilization did not have to be directly +met, the asexual spores germinating without it. The greater the +number of these produced, the better the chance that at least some of +the gametes developed from them would meet the difficult conditions +of fertilization, and the survival of the species be assured. At the +same time, in order to meet the requirements of terrestrial life +successfully, and to provide for continuing the sexual generation, +correlative changes would have to take place in the gametophyte by +which the increasing uncertainty of fertilization due to structural +changes in the sporophyte, and the absence of a liquid medium for +the conveyance of free swimming antherozoids would be avoided. This +necessity has been met by the development of the pollen tube, which +bores its way to the egg cell, carrying with it the generative cells, +which in seed plants have taken the place of the more primitive +antherozoids. With the concomitant reduction of the gametophyte and +development of the seed habit, the adaptation to land conditions has +been made complete. + +Roughly speaking, it may be said: (1) that Thallophytes are +predominantly aquatic; (2) Archegoniates (Bryophytes and +Pteridophytes), amphibious; (3) Spermophytes, terrestrial; (4) that +the seed habit is a response to terrestrial conditions; and (5) +that the increased development of the sporophyte was a necessary +adaptation to meet those conditions. + + + IX. THE COURSE OF PLANT EVOLUTION + +=417. Plant genealogy.=—It has been shown by a study of existing +forms of plant life that there is no hard and fast line of division +anywhere between the different groups, but that they are all +connected by ties of kinship more or less defined, according to their +distance from a common ancestral stock. The geological record points +to the same conclusion, and our classification of them into families, +orders, and species is merely a very imperfect genealogical table +of their supposed pedigrees. This does not mean, however, that we +can assert positively that such and such a species is derived from +such or such another, but that both are descended from some common +intermediate form more or less remote. While we have reason to +believe that the flowering plants are derived through pteridophyte +and bryophyte types from some of the green algæ, no direct connection +has ever been traced between any particular kind of flowering +plant and any particular kind of alga,—or between a liverwort and +an alga, for that matter,—and probably never will be, because the +intermediate forms die out, or pass on by variation into other lines +of development. But while this is true, all the evidence we possess +does go to show that, since the beginning of life on the globe, there +has been a general progressive evolution from lower and simpler to +higher and more complex forms. + +=418. Retrogressive evolution.=—While the general course of evolution +has been upward and onward, the movement has not always followed +a straight line, but, like a mountain road, shows many windings +and deviations from the direct route. The monocotyls furnish a +conspicuous example of this departure from the general law of +progression. It was formerly supposed, on account of their greater +simplicity of structure, that they were a more ancient type than +dicotyls, but recent investigations point to the conclusion that +they are a later offshoot, derived from some primitive form of +aquatic dicotyl, and represent, not an ancient and primitive stock, +but a case of retrogressive evolution from a higher type. Strong +presumptions in favor of this view are: (1) that various species of +dicotyls show an unequal development of the seed leaves, amounting, +in the bryony, to complete abortion of one of them, while some +monocotyl seeds show morphological characters that can best be +explained as survivals, or inheritances, from a dicotyl ancestor; +(2) the structural resemblances between gymnosperms and dicotyls are +closer than between gymnosperms and monocotyls, which could hardly +be the case if the latter were the more ancient; (3) the geological +record does not show them to have appeared before dicotyls; (4) the +number of cotyledons furnishes no criterion as to the relative age +of any plant group, since all three types are represented among the +pteridophytes, where plants are found bearing one, two, or more +cotyledons. + +The theory of their comparatively recent origin from an aquatic +ancestor is further borne out by the many points of similarity +between their internal structure and that of hydrophytes (318), and +also by the great proportion of aquatic plants among them, amounting +to thirty-three per cent, while in dicotyls the proportion is only +four per cent. Can you give any reasons, from your examination of +their internal structure (113, 114), for believing that the line of +development which they have followed is a less effective one for +meeting conditions now existing on the globe than that attained by +dicotyls? + +We should remember, too, that while progressive evolution implies +successful adjustment to surroundings, it is possible to conceive of +a state, as our planet approaches the period of cosmic debility and +decay, when the conditions of existence may become progressively more +and more unfavorable. In this case the course of evolution would be +reversed, the higher types gradually dying out as the struggle for +life became more severe, and the tendency would be constantly toward +lower and simpler forms, until finally all life would become extinct +on our planet. We have no right, however, to assume that during such +a course of retrogressive evolution the same forms would be repeated +in reverse order as have already appeared, because there is no reason +to believe that the conditions brought about by planetary decline and +“old age” would be the same as those attending planetary birth and +adolescence. + +[Illustration: FIG. 511.—Diagram showing the supposed course of plant +evolution.] + +=419. Explanation of the diagram.=—An attempt to show the general +course of plant evolution up to the present time is made in the +accompanying diagram. The four great divisions, Thallophytes, +Bryophytes, Pteridophytes, and Spermatophytes, are represented by +spaces between four horizontal lines arranged one above the other in +the order of their succession in time and complexity of organization. +It should be borne in mind that these dividing lines are not sharply +defined in nature, but overlap or indent the territory between them +with varying degrees of irregularity, like the coast line on a +map. The relative positions of the different orders we have been +considering are represented by upright and diagonal lines, the +general course of which, as indicated by the arrows, is intended to +give an idea of the trend of evolutionary progress in the particular +group represented by each line. No one of these lines is made to +originate directly in any other, because, with the possible exception +of the monocotyls, we have no authority for asserting that any such +direct connection exists between plants as we know them, but only +that certain types give evidence of descent from a common ancestry. +This lack of certainty is expressed by placing the point of origin +for any given line in more or less close proximity to the one which +is supposed to be the nearest living representative of the common +ancestor. The line of ferns, for instance, is depicted as originating +in the region of the bryophytes, somewhere in the neighborhood of +the liverworts, but the two lines nowhere come in contact, because +there is no evidence that any fern, living or fossil, is directly +descended from any particular kind of liverwort known to us. With +these explanations, the diagram shows, in a rough way, the generally +accepted view of plant relationships as based on the evidence at +present before us. But in questions of this sort it is wise to keep +in mind the blunt remark of a famous old American statesman, that +“only fools and dead people never change their opinions.” + + + Field Work + + 1. If you live in the country, study the appearance of plants + affected with blights, smuts, rusts, and mildews, and learn to + recognize the different kinds of disease by their signs. Notice + which kinds are most prevalent in your neighborhood, and what + plants are most affected by them. + + 2. Notice the different kinds of mushrooms you find growing wild. + Observe the difference between those that grow on the ground and + those that grow on logs, stumps, and trees; between those found + in the woods and those in open ground. Find out how those on the + ground get their nourishment. Uncover the mycelium, and notice + the extent of its surface. Examine the soil and find out if it + contains anything upon which they could feed. Note the prevalence + of shelf fungi on trees. Examine the condition of the wood where + they grow, and decide in what ways they injure their hosts. Notice + whether they abound most on healthy or on decaying trunks and + boughs, and decide whether this is because the fungus prefers that + kind of host, or whether the injury it does causes the decay, or + whether both causes operate together. Notice what fungi grow on + different trees, and study their preferences in this respect. + + 3. Observe the different kinds of lichens found in your walks + and try to distinguish the three classes. Which kind are most + abundant in your neighborhood? Which least so? Note the situations + in which you find each kind growing, whether on stumps, trees, + rocks, or the ground. Consider how the algæ and fungi aid each + other in the different positions; could either, for instance, exist + independently on bald rocks? Notice on what kind of trees the + different lichens seem to thrive best and on which poorly or not at + all, and whether the character of the bark—rough, smooth, scaly—has + anything to do with their choice of a habitat. + + + + +APPENDIX + + + + + SYSTEMATIC BOTANY + + +=Taxonomy, or systematic botany=, deals with the family relationships +of plants in the order of their nearness or remoteness with regard +to a common line of descent. Its chief value is the insight it +gives into the course of plant evolution and into the nature of +the modifications that differentiate each group from the ancestral +type. While it is not advisable to spend too much time in the mere +identification of species, a sufficient number should be examined +and described to familiarize the student with the distinctive +characteristics of the principal botanical orders. + +=Principles of classification.=—All the known plants in the world, +numbering not less than one hundred and twenty thousand species +of the seed-bearing kind alone, are ranged according to certain +resemblances of structure, into a number of great groups known as +families or orders. The names of these families are distinguished by +the ending _aceæ_; the rose family, for instance, are the _Rosaceæ_; +the pink family, _Caryophyllaceæ_; the walnut family, _Juglandaceæ_, +etc. Each of these families is divided into lesser groups called +_genera_ (singular, _genus_), characterized by similarities showing +a still greater degree of affinity than that which marks the larger +groups or orders; and finally, when the differences between the +individual plants of a kind are so small as to be disregarded, they +are considered to form one species; all the common morning-glories, +for instance, of whatever shade or color, belong to the species +_Ipomea purpurea_. The small differences that arise within a species +as to the color and size of flowers, and other minor points, +constitute mere varieties, and have no special names applied to them. +The line between varieties and species is not clearly defined, and +in the nature of things can never be, since progressive development, +through unceasing change, is the law of all life. + +In botanical descriptions, the name both of the species and the genus +is given, just as in designating a person, like Mary Jones or John +Robinson, we give both the surname and the Christian name. The genus, +or generic name, answers to the surname, and that of the species to +the Christian name—except that in botanical nomenclature the order +is reversed, the generic, or surname, coming first, and the specific +or individual name last; for example, _Ipomea_ is the generic, or +surname, of the morning-glories, and _purpurea_ the specific one. + +=How to use the key.=—Any good manual will answer the purpose. Gray’s +“School and Field Book” is, perhaps, the best available at present +for the states east of the Mississippi. Reference to the floral +analyses in sections =I-IV= of Chapter VII will make its use clear. +Suppose, for instance, we want to find out to what botanical species +the morning-glory or the sweet potato belongs. Turning to the key, +we find the sub-kingdom of Phænerogams—flowering or seed-bearing +plants—divided into two great classes, Angiosperms and Gymnosperms, +as explained in 18. A glance will show that our specimen belongs +to the former class. Angiosperms, again, are divided into the two +subclasses of Dicotyledons and Monocotyledons (18, 171). We at +once recognize our plant, by its net-veined leaves and pentamerous +flowers, as a dicotyledon (171, 229), and turning again to the key, +we find this subclass divided into three great groups: Sympetalous +(211), called also Monopetalous and Gamopetalous; Apopetalous, or +Polypetalous (211), and Apetalous—having no petals or corolla. A +glance will refer our blossom to the sympetalous or monopetalous +group, which we find divided into two sections, characterized by +the superior or inferior ovary (218, 225). Further examination will +show that the morning-glory belongs to the former class, which is +in turn divided into two sections, according as the corolla is +_regular_, or _more or less irregular_. We see at once that we must +look for our specimen in the group having regular corollas. This we +find again subdivided into four sections, according to the number and +position of the stamens, and we find that the morning-glory falls +under the last of these,—“Stamens as many as the lobes or parts of +the corolla and alternate with them.” A very little further search +brings us to the family _Convolvulaceæ_, and turning to that title +in the descriptive analysis, we find under the genus, _Ipomea_, a +full description of the common morning-glory, in the species _Ipomea +purpurea_, and of the sweet potato in the species _Ipomea batatas_. + +=Making collections.=—Mere labeled aggregations of species are not +recommended, but the collection of examples illustrating special +points in morphology and plant variation may be made with profit; +such, for instance, as the adaptations observed in tendrils and +stipular appendages, the various modifications of leaves and stems +to serve other than their normal purposes, or the different forms +of leaves and flowers on the same stem, or on different plants of +the same species. A collection made with some specific object in +view would also be instructive, and might prove of great value; for +instance, to get together examples of all the troublesome weeds of +a locality for the purpose of studying their habits and devising +means for their eradication; or of all the native useful plants, with +detailed analyses of their economic properties, and observations on +their habits and the practicability of further developing them. In +short, wherever collecting is carried on, it should be done with some +object other than the mere identification of species, which often +results in greater detriment to the wild plants of a neighborhood +than profit to the collector. + + + + + WEIGHTS, MEASURES, AND TEMPERATURES + + +As the metric system of weights and measures and the Centigrade +appraisement of temperatures are universally employed in scientific +works, the following tables showing the equivalents in our common +English standards of those in most frequent use, are given for the +convenience of students who have not already familiarized themselves +with the subject. The values given are approximate only, but will +answer for all practical purposes, except in cases where very +great exactitude is required. The micron, or micrometer, is used +principally by scientific investigators for measuring extremely +minute objects seen under the microscope. + + + MEASURES OF LENGTH + + ================================+===================================== + METRIC | ENGLISH EQUIVALENTS + -----------------+--------------+------------------------------------- + Kilometer | km. | ⅔ of a mile. + -----------------+--------------+------------------------------------- + Meter | m. | 39 inches. + -----------------+--------------+------------------------------------- + Decimeter | dm. | 4 inches. + -----------------+--------------+------------------------------------- + Centimeter | cm. | ⅖ of an inch. + -----------------+--------------+------------------------------------- + Millimeter | mm. | ¹⁄₂₅ of an inch. + -----------------+--------------+------------------------------------- + Micron | µ | ¹⁄₂₅₀₀₀ of an inch. + -----------------+--------------+------------------------------------- + + + CAPACITY + + -----------------+---------+------------------------------------------ + Liter | l. | 61 cubic inches, or 1 quart, U.S. measure + -----------------+---------+------------------------------------------ + Cubic centimeter | cc. | ¹⁄₁₆ of a cubic inch. + -----------------+---------+------------------------------------------ + + + WEIGHT + + -----------------+---------------+------------------------------------ + Kilogram | kg., or kilo. | 2⅕ pounds. + -----------------+---------------+------------------------------------ + Gram | gm. | 15½ grains avoirdupois. + | | ¹⁄₂₈ of an ounce avoirdupois. + =================+===============+==================================== + + + METRIC AND ENGLISH SCALES + +[Illustration: 10 CENTIMETERS = 1 DECIMETER + +100 MILLIMETERS + +4 INCHES] + + + TEMPERATURE EQUIVALENTS + +The next table gives the Fahrenheit equivalent, in round numbers, for +every tenth degree Centigrade from absolute zero to the boiling point +of water. To find the corresponding F. for any degree C., multiply +the given C. temperature by nine, divide by five, and add thirty-two. +Conversely, to change F. to C. equivalent, subtract thirty-two, +multiply by five, and divide by nine. + + Cent. Fahr. + ---------------- + 100 212 + 90 194 + 80 176 + 70 158 + 60 140 + 50 122 + 40 104 + 30 86 + 20 68 + 10 50 + 0 32 + −10 14 + −20 −4 + −30 −22 + −40 −40 + −50 −58 + −100 −148 + ———————————————— + Absolute zero. + -273 -459 + + + + +FOOTNOTES: + +[1] Vines, “Lectures on the Physiology of Plants,” p. 282. See also +Sachs, “Physiology of Plants.” + +[2] Marshall Ward, “The Oak.” + + + + +INDEX + +(The numbers, unless otherwise designated, refer to paragraphs.) + + + Aborted, 220, 291. + + Absorption, 58, 71, 72; Exp. 39. + selective, 60. + + Accessory buds, 158. + + Accessory fruits, 302. + + Adaptation, 206, 237. + + Adhesive fruits, 20; Exp. 20. + + Adjustment of leaves, 196-202. + + Adnate, 374. + + Adventitious buds, 65, 158. + + Adventitious roots, 37, 83. + + Æcidium, 362. + + Aëration, 319. + + Aërial roots, 88. + + Aggregate fruits, 301, 303. + + Air space, 114, 116, 184. + + Akene, 234, 296, 302, 305. + + Albumin, 3. + + Albuminous, 56. + + Albuminous seed, _i.e._, containing endosperm; + Field work, p. 28. + + Aleurone, 3. + + Algæ, 333, 336-342. + + Alternate leaves, 168. + + Alternation of generations, 395, 400, 409, 414. + + Analogous, 108. + + Anatropous, Fig. 26. + + Angiosperms, 15, 18; Fig. 511. + + Annuals, 91. + + Annulus, 372, 405. + + Anther, 213, 235; Figs. 270-274. + + Antheridia, 389, 394, 398, 407. + + Antheridial, 388. + + Antherozoids, 389, 392, 395, 416. + + Antisepsis, 355. + + Arch of the hypocotyl, 42, 44. + + Archegonia, 390, 394, 407, 408. + + Archegonial, 388. + + Archegoniates, 408, 416. + + Archegonium, 391, 394, 398. + + Asexual generation, 395, 399, 409, 416. + + Asexual reproduction, 394, 395. + + Asexual spore, 395, 407, 409, 410, 416. + + Assurgent, 95. + + Axial placenta, 216, 300. + + Axil, 100, 166. + + Axillary buds, 145. + + Axis, 64, 65, 79, 152, 156, 159, 161. + + + Bacillus, 348, 349. + + Bacteria, 333, 345, 347-353. + + Bark, 118, 119, 122, p. 128, (3). + + Basidia, 375. + + Bast, 116, 119, 122. + + Berry, 291. + + Biennial, 92. + + Bilabiate, 237, 243. + + Bilateral regularity, 219. + + Bilateral zonation, 326. + + Black rust, 360. + + Blade of leaf, 165. + + Biogenetic law, 253. + + Biological factors, 309. + + Bordered pits, 114, 117; Fig. 123. + + Boreal, 329. + + Bract, 161. + + Bryophytes, 334, 385-401. + + Bud scales, 147-149. + + Buds, 145, 155-158. + + Bulb, 107. + + Button (of mushroom), 370. + + + Calyptra, 399. + + Calyx, 211. + + Cambium, 115, 116, 120, 123. + + Cap, 372, 373. + + Capillarity, 136; Exp. 53. + + Capitate, 220. + + Caprification, 279, 305. + + Caprifig, 279. + + Capsule, 298. + + Carbon, 27, 28, 62. + + Carbon dioxide, 29, 63, 185, 186, 187, 189; Exps. 23, 25. + + Carpels, 216, 288. + + Caruncle, 13. + + Catkin, 161. + + Caulicle, 46. + + Cedar apples, Fig. 456. + + Cell, 6, 7. + collecting, 184. + companion, 114. + + Cell sap, 7, 110. + + Cell wall, 7, 183. + + Central cylinder, 67. + + Central placenta, 216, 300. + + Chalaza, 13. + + Chlorophyll, 186, 341, 366. + + Chlorophyll bodies, 184, 186, 382. + + Cion, 65. + + Classification, 90, 252, 283, 343, 384, 411, 417. + + Cleistogamic flowers, 272. + + Climatic zones, 329. + + Climbing stems, 96-98. + + Clipped seed, p. 12 (material). + + Closed bundle, 114. + + Close-fertilized, 272. + + Cluster cups, 362. + + Coccus (pl. cocci), 339, 348. + + Coiled inflorescence, 162. + + Collective fruits, 304. + + Colony, 316, 337, 357. + + Color of flowers, 276. + + Compass plants, 199. + + Complete flower, 219. + + Composite, 235, 381. + + Composite flower, 236. + + Compound leaf, 178. + + Conduplicate, Figs. 159, 160. + + Confluent, 404. + + Conifers, 117, 327. + + Conjugation, 342, 394. + + Corolla, 211. + + Cortex, 64, 115, 122. + + Corymb, 161. + + Cotyledon, 11, 12, 18. + + Cross cut, 133. + + Cross fertilization, 255. + + Cross pollination, 255. + + Crustaceous lichen, 384. + + Cryptogam, 332. + + Crystalloids, 60. + + Culture medium, 347; p. 306 (material). + + Cycle, 217, 219, 229. + + Cycle of growth, 50. + + Cyme, 162. + + Cymose inflorescence, 162. + + Cypress knees, 319. + + + Deciduous, 203. + + Declined, 95. + + Decurrent, 374. + + Definite annual growth, 153. + + Definite inflorescence, 160, 162. + + Dehiscent fruits, 283, 298. + + Deliquescent, 144. + + Determinate growth, 153. + + Determinate inflorescence, 160, 162. + + Diadelphous, 239. + + Diastase, 9. + + Dichogamy, 269. + + Dichotomous, 152; Fig. 155. + + Dicotyl, 42, 115, 116, 171, 220. + + Dicotyledonous, 12. + + Differentiate, 245, 345, 409. + + Diffusion, 9, 57. + + Digestion, 9. + + Dimorphic, 270. + + Dimorphism, 270. + + Dimorphous, 270. + + Diœcious, 268. + + Disinfection, 355. + + Disk flower, 233. + + Dispersal of seed, 19-25. + + Dominant, 257, 258. + + Dormant buds, 157. + + Dorsal; Figs. 390, 391. + + Drupe, 292. + + Dry fruits, 283, 293-300. + + Duct, 67, 111, 114. + + + Ecological factors, 310. + + Ecology, 266, 308, 310. + + Edgings, 134. + + Egg cell, 251, 391. + + Elators, 393. + + Embryo, 11. + + Embryology, 253. + + Embryo sac, 251. + + Endodermis, 67 (b). + + Endosperm, 11, 13, 14, 16, 17, 414. + + Epicotyl, 45, 46, 47. + + Epidermis, 64, 115, 122, 183. + + Epigynous, 225, 230. + + Epiphyte, 87, 394. + + Essential constituents, 62. + + Essential organs, 212. + + Evolution, 242, 245, 265, 334, 335, 401, 414, 415, 417, 418, 419. + + Evolutionary, 253, 413. + + Excentric attachment, 372. + + Excurrent, 144, 154. + + + Factors, 54, 265, 310. + + Fall of the leaf, 203. + + Fascicled roots, 80, 81. + + Fats, 1, 3, 4. + + Feather-veined, 172. + + Ferments, 9, 356. + + Fertile, 404. + + Fertile flower, 267. + + Fertilization, 247, 251, 252, 392, 408, 416. + + Fibrous roots, 37, 78, 80, 81. + + Fibrovascular bundle, 67, 114, 116, 176, 288. + + Fig wasp, 279. + + Filament of the stamen, 213; + a hairlike appendage, 341, 361, 369, 393, 396. + + Filamentous algæ, 340, 341. + + Fission, 338, 394. + + Fleshy fruits, 283, 288-292. + + Floral envelopes, 211. + + Foliaceous lichen, 379, 384. + + Follicle, 298. + + Forestry, 139-142. + + Forked stems, 152. + + Formation, 316. + + Free, 218, 374. + + Free central placenta, 216. + + Free gills, 374. + + Free ovary, 218. + + Free veining, 402. + + Freezing, 33. + + Frog’s spit, 340. + + Frond, 402. + + Fruit, 282. + + Fruticose lichen, 384. + + Function, 41. + + Fungi, 333, 343, 344, 345, 346, 378. + + Fungus, 86, 364. + + + Gametes, 394. + + Gametophyte, 394, 395, 396, 406, 407, 410, 412, 414, 415, 416. + + Gemmæ, 387. + + Generative cell, 249, 416. + + Geophilous, 321. + + Geotropism, 51, 52, 53. + + Germ, 2, 11. + + Germ cell, 251, 414. + + Germination, 32, 35; Exps. 25, 26-29. + + Germs, 352, 355. + + Gills (of mushroom), 374. + + Girdling, 131. + + Glutin, 3. + + Gourd, 14, 290. + + Grain, 11, 297. + + Grain of timber, 133, 134, 135. + + Gravity, 52. + + Growth, 48-52, 179. + + Guard cell, 183. + + Gymnosperms, 15, 18, 117, 414. + + Gymnosporangium, Fig. 456. + + + Halophyte, 317, 323. + + Haustoria, 85. + + Hay bacillus, 348, 349. + + Head, 161. + + Heartwood, 131. + + Heliotropic, 200. + + Heliotropism, 198. + + Herbaceous, 90, 94, 115, 116. + + Heredity, 264, 265. + + Hilum, 12, 13, 14. + + Homologous, 108. + + Host plant, 85. + + Humus, 75, 86. + + Hybrid, 256. + + Hybridization, 256, 257, 263. + + Hydrophytes, 317, 318, 319. + + Hymenium, 375. + + Hymenomycetes, 375. + + Hyphæ (sing. hypha), 369, 380. + + Hypocotyl, 11, 12, 14, 46. + arched, 42, 44. + straight, 44. + + Hypogynous, 218, 225. + + + Imbibition, 136. + + Imperfect flower, 219, 231, 267. + + Impure hybrid, 258, 259. + + In-breeding, 254. + + Incomplete flower, 219. + + Incubation, 354. + + Indefinite annual growth, 153. + + Indefinite inflorescence, 160, 161. + + Indefinite number of parts, 229. + + Indehiscent fruit, 283, 294. + + Indeterminate growth, 153. + + Indeterminate inflorescence, 160, 161. + + Indusium, 404. + + Inferior ovary, 221, 225. + + Inflorescence, 159. + + Insectivorous plants, 208-210. + + Internode, 46, 110; Exp. 35. + + Invasion, 328. + + Inverted seed, 14. + + Involucre, 161, 232. + + Involute, 373; Fig. 251. + + Iodine solution, Exp. 3. + + Irregular flower, 219, 237. + + Irritability, 201. + + + Joint, 110, 113. + + + Keel, 238. + + Knots, 137. + + + Lamina, 209. + + Laminæ, 368, 374. + + Lateral, 372, 398. + + Lateral buds, 145. + + Leaf attachment, 167. + + Leaf cups, 202. + + Leaf scars, 146. + + Leaf traces, 146. + + Legume, 299. + + Lenticels, 106, 118, 288. + + Lichen, 379. + + Life cycle, 359, 364. + + Loam, 75. + + Lobing, 177; Figs. 210-212. + + Locule, 216. + + Loment, Fig. 394. + + Lyrate, Fig. 197. + + + Medulla, 119, 122. + + Medullary rays, 64, 116, 121, 122, 134, 135. + + Megasporangia, 409. + + Megaspore, 409, 414. + + Mendel’s law, 258. + + Mesophyte, 317, 324. + + Metabolism, 193. + + Microbe, 351, 355. + + Micrococcus, 339. + + Micropyle, 12, 13, 14, 15, 45. + + Microsporangia, 409. + + Microspore, 409, 414. + + Midrib, 172. + + Mixed forest, 139, 324. + + Modification, 100-108, 206, 207, 289. + + Molecule, 136. + + Monadelphous, 239. + + Monocotyl, 110, 112, 171, 217, 221, 418. + + Monocotyledonous, 11. + + Monœcious, 268. + + Monopetalous, 211. + + Monosepalous, 211. + + Morphology, 108. + of the flower, 244. + + Mosaic (leaf), 197. + + Mosses, 334, 396-401. + + Muck, 75. + + Multiple fruit, 304, 305. + + Mushroom, 333, 367. + + Mutation, 264. + + Mycelium, 343, 359, 369. + + Mychorrhiza, 86. + + + Neck canal, 391. + + Net-veined, 171. + + Neuter, 267. + + Neutral flower, 231, 267. + + Nitrogen, 62, 63, 188. + + Nitrogenous food, 188. + + Node, 46, 65, 110, 113. + + Nucleus, 7, 341. + + Numerical plan, 217, 229. + + Nut, 295. + + Nutriment, 3, 186. + + Nutrition, 50, 54, 179, 193. + + Nyctitropic, 200. + + + Obsolete, 220. + + Oil, 1, 3, 8. + + Oöspore, 393, 394, 395. + + Open bundle, 116. + + Operculum, 399. + + Opposite leaves, 168. + + Organ, 41. + + Organic foods, 4. + + Organs of reproduction, 40. + of vegetation, 40. + + Osmosis, 56, 57. + + Ovary, 214, 216, 223. + + Ovule, 216. + + Oxidation, 27; Exps. 21, 22. + + Oxygen, 62, 63, 186, 187; Exps. 22, 66. + + + Palisade cells, 184. + + Palmate veining, 172. + + Panicle, Fig. 171. + + Papilionaceous, 237, 238. + + Pappus, 234. + + Parallel veining, 171. + + Paraphyses, 375, 398. + + Parasitic, 5, 345, 364. + + Parasitic plants, 85, 343, 382. + + Parenchyma, 110, 114, 115. + + Parietal, 216. + + Pathogenic, 352, 353. + + Pedicel, 159. + + Peduncle, 159, 288. + + Pentamerous, 229. + + Pepo, 290. + + Perennial, 93. + + Perfect flower, 219. + + Perianth, 211. + + Pericarp, 288. + + Perigynous, Figs. 301, 302. + + Persistent, 166. + + Petals, 211. + + Petiole, 165. + + Phanerogams, 331, 332. + + Phloem, 114, 116. + + Photosynthesis, 186, 192, 193. + + Phototropism, 195. + + Phyllotaxy, 168, 169. + + Pileus, 373. + + Pinna, 402. + + Pinnate veining, 172. + + Pinnule, 402. + + Pioneer plant, 316, 319, 320. + + Pistil, 212, 214, 223, 228, 240. + + Pistillate, 267. + + Pitcher plant, 209. + + Pith, 110, 115, 116, 119, 121, 122. + + Pitted ducts, 114. + + Placenta, 216, 288, 298, 300. + + Plant society, 316. + + Plasmolysis, 59. + + Pleurococcus, 337. + + Plicate, 155. + + Plumule, 11, 12, 14, 45, 46. + + Pod, 298. + + Pollen, 213. + + Pollen grains, 213. + + Pollen sac, 213. + + Pollen tubes, 249, 250. + + Pollination, 215, 247. + + Polycotyledons, 15, 45. + + Polymorphic, 365. + + Polymorphism, 365. + + Polypetalous, 211. + + Polysepalous, 211. + + Pome, 288. + + Prefoliation, 155. + + Primary, 396. + + Primary root, 42, 79. + + Pronuba, 278. + + Prostate, 95. + + Protection, 199, 204, 207, 280, 287. + + Proteins, 3, 8, 33, 188, 204. + + Prothallium, 407. + + Protonema, 396. + + Protoplasm, 6, 7, 57, 58, 67, 110, 116. + + Pteridophytes, 335, 411, 412. + + Puccinia, 360. + + Pure dominant, 258, 259. + + Pure forest, 139, 324. + + Pure recessive, 258, 259. + + Pycnidia, 363. + + + Quartered cut, 135. + + + Raceme, 161. + + Rhachis, 178. + + Radial section, 132, 135. + + Radicle, 46. + + Rhaphe, 13. + + Ray, 161, 391. + + Ray flowers, 231. + + Receptacle, 211, 288, 289, 388, 390, 398. + + Recessive, 257, 258. + + Red rust, 359. + + Regular flower, 219. + + Reproduction, 338, 351, 358, 383. + + Respiration, 30, 31, 191, 192. + + Resting spore, 338, 342, 358, 394. + + Reticulation, 172, 402. + + Retrogressive evolution, 418. + + Revolute, 373, 404. + + Rhizoids, 379, 386. + + Rhizome, 105. + + Ringing, 127. + + Rings of growth, 122, 123, 134, 135. + + Rogue, 260. + + Root cap, 39. + + Root hairs, 38, 67. + + Root pressure, Exp. 49. + + Root pull, 69. + + Rootstock, 105. + + Root system, 89. + + Root tubercles, 63, 300. + + Rosette, 197. + + Rotation of crops, 24, 327. + + Runner, 95. + + + Samara, 296. + + Sap movement, 125, 126, 128, 129. + + Saprophyte, 86. + + Sapwood, 131. + + Scale leaves, 101, 106, 107, 147-149, 207. + + Scape, 107, 159. + + Scorpioid inflorescence, 162; Figs. 173-176. + + Screenings, 20; p. 28, Qn. 22. + + Secondary roots, 37, 42, 79. + + Seed, 11-18, 332, 415. + + Seed coat, 12, 14, 15, 43. + + Seedless fruits, 285, 286. + + Seedlings, 36, 42, 43, 45. + + Seed plants, 331, 414. + + Seed vessel, 282. + + Selection, 260, 265, 286. + artificial, 262. + natural, 261. + + Self-fertilization, 254, 271. + + Sepals, 211. + + Sessile, 167, 214. + + Seta, 399. + + Sexual generation, 395, 396, 406, 410, 416. + + Sexual reproduction, 394, 395, 410. + + Sheath, 67, 116. + + Shrinking of timber, 136. + + Sieve tube, 114. + + Slabs, 134. + + Sleep movements, 200. + + Soils, 75, 77. + + Sori, 404. + + Spathe, 221. + + Specialization, 237. + + Spermatophytes, 331, 335, 394, 414. + + Spermatozoid, 389. + + Spermogonia, 363. + + Spike, 161. + + Spirillum, 348. + + Spirogyra, 341. + + Sporangia, 390, 405. + + Spore, 332, 349, 350, 377, 406, 410. + + Spore case, 390, 393, 405. + + Spore print, 376. + + Sporidium, 361. + + Sporogonium, 393, 399. + + Sporophyll, 406, 414. + + Sporophyte, 393-395, 399, 406, 410, 412, 414, 416. + + Sport, 264. + + Stamen, 212, 213. + + Staminate, 267, 268. + + Staminodia, 244. + + Standard, 238. + + Starch, 3, 4, 187, 204, 288; Exps. 69, 70. + + Stems, 90-99. + + Sterile flower, 267. + + Sterilization, 354. + + Stigma, 214. + + Stigmatic surface, 223. + + Stimulus, 98, 186, 201. + + Stipe, 240, 372, 402. + + Stipule, 149, 165, 166. + + Stolon, 95. + + Stoma, 181, 182, 183. + + Stomata, 181, 182. + + Stone fruit, 292. + + Storage of food, 2, 3, 4, 17, 70, 103, 104-107, 287. + + Strangling fig, 88. + + Strobile, 411. + + Strobiliaceous, 411. + + Style, 214. + + Succession, 327. + + Sugars, 3, 4, 204, 288. + + Summer spores, 360. + + Sundew, 210. + + Superior ovary, 218, 221, 225. + + Supernumerary buds, 158. + + Suppressed, 220. + + Survival of the fittest, 261. + + Suture, 216, 298, 299. + + Swarm spore, 349. + + Swelling of timber, 136. + + Symbiosis, 309, 382. + + Symmetrical flower, 219. + + Sympetalous, 211. + + Syncarpous, 300. + + Synsepalous, 211. + + Systematic botany, _see_ Appendix. + + + Tangential cut, 132, 134. + + Tap root, 79. + + Teleutospore, 360. + + Tendril, 96, 97. + + Terminal bud, 145, 154. + + Testa, 14. + + Thallophytes, 333. + + Thallus, 333, 341, 343, 379, 380, 381, 385. + + Tillage, 76. + + Tissue, 60, 61. + + Toadstools, 367. + + Toxins, 345. + + Tracheids, 114, 117. + + Trailing, 95. + + Trama, 375. + + Transpiration, 179, 180. + + Trifoliolate, Figs. 215, 216. + + Trimerous, 217. + + Trimorphic, 270. + + Tuber, 106. + + Tumbleweeds, 23. + + Turgidity, 7. + + Turgor, 179. + + Twining, cause of, 98; Exp. 55. + + Twining stems, 96; Exp. 54. + + Type, 18, 260, 263, 265, 336, 411. + + + Umbel, 161. + + Umbonate, 373. + + Underground stems, 104-107. + + Unicellular, 337. + + Unisexual, 267. + + Uredo, 359. + + Uredospore, 359, 360. + + + Variation, 263, 264, 265. + + Vascular bundles, 111. + + Vascular cryptogams, 403, 411, 412. + + Vascular cylinder, 64. + + Vascular system, 111, 113, 335. + + Vegetative reproduction, 358. + + Veil, 371. + + Veins, 173-176. + + Venter, 391. + + Ventral, Figs. 390, 391. + + Vernation, 155. + + Vessels, 111. + + Vexillum, 238, 239. + + Vibrio, 348. + + Vitality of seeds, 34; Exp. 30. + + Volva, 371. + + + Water roots, 39, 84. + + Whorled leaves, 168. + + Wind pollination, 274, 275. + + Wings, 238. + + Winter spores, 360. + + + Xerophyte, 317. + + Xerophyte societies, 317, 320-322. + + Xylem, 114, 116. + + + Yeast, 356. + + Yeast colony, 357. + + Yellow trumpets, 209. + + Yucca, 278. + + Yucca moth, 278. + + + Zonation, 325, 327. + bilateral, 326. + concentric, 326. + horizontal, 326. + vertical, 326. + + Zones of vegetation, 325. + + + + +TRANSCRIBER’S NOTE + + + Obvious typographical errors and punctuation errors have been + corrected after careful comparison with other occurrences within + the text and consultation of external sources. + + Some hyphens in words have been silently removed, some added, + when a predominant preference was found in the original book. + + Except for those changes noted below, all misspellings in the text, + and inconsistent or archaic usage, have been retained. + + p. 45: ‘many of them has’ amended to ‘many of them have’ + p. 281: ‘are adpated’ amended to ‘are adapted’ + p. 291: ‘and as it can, moveover’ amended to ‘and as it can, moreover’ + p. 354: ‘eruption of Krakatao’ amended to ‘eruption of Krakatoa’ + + + + +*** END OF THE PROJECT GUTENBERG EBOOK 78430 *** diff --git a/78430-h/78430-h.htm b/78430-h/78430-h.htm new file mode 100644 index 0000000..c992477 --- /dev/null +++ b/78430-h/78430-h.htm @@ -0,0 +1,20037 @@ +<!DOCTYPE html> +<html lang="en"> +<head> + <meta charset="UTF-8"> + <title> + A practical course in botany | Project Gutenberg + </title> + <link rel="icon" href="images/cover.jpg" type="image/x-cover"> + <style> + +body { + margin-left: 10%; + margin-right: 10%; +} + + h1,h2,h3,h4 { + text-align: center; /* all headings centered */ +} + h1 {font-weight: normal;} + h2 {font-weight: normal; font-size: 130%;} + h3 {font-size: 100%;} + +h2 { margin-top: 3em; } + +h3 { margin-top: 2em; } + +p { + margin-top: .51em; + text-align: justify; + margin-bottom: .49em; + text-indent: 1em; +} + +.p2 {margin-top: 2em;} +.p4 {margin-top: 4em;} +.pad2 {padding-left: 2em;} +.pad6 {padding-left: 6em;} +.mth { margin-top: .5em;} +.pad-chap {padding-top: 1.5em; padding-bottom: .5em;} +.noindent {text-indent: 0em;} +.pl1 { padding-left: 1em; } + +.fs120 {font-size: 120%;} +.fs100 {font-size: 100%;} +.fs90 {font-size: 90%;} +.fs80 {font-size: 80%;} +.fs60 {font-size: 60%;} + +.cb { clear: both; } + +hr { + width: 33%; + margin-top: 2em; + margin-bottom: 2em; + margin-left: 33.5%; + margin-right: 33.5%; + clear: both; +} + +hr.chap {width: 65%; margin-left: 17.5%; margin-right: 17.5%;} +@media print { hr.chap {display: none; visibility: hidden;} } +hr.r5 {width: 5%; margin-top: 1em; margin-bottom: 1em; margin-left: 47.5%; margin-right: 47.5%;} + +div.chapter {page-break-before: always;} +h2.nobreak {page-break-before: avoid;} + +ul.index { list-style-type: none; } +li.ifrst { + margin-top: 1em; + text-indent: -2em; + padding-left: 1em; +} +li.indx { + margin-top: .5em; + text-indent: -2em; + padding-left: 1em; +} +li.isub1 { + text-indent: -2em; + padding-left: 2em; +} + +table { + margin-left: auto; + margin-right: auto; +} +table.autotable { border-collapse: collapse; } +td { padding: 0.3em; } + +.tdl {text-align: left; padding-left: 1em;} +.tdr {text-align: right;} +.tdc {text-align: center;} +.wd20 {width: 20%;} +.wd30 {width: 30%; text-align: justify;} +.wd33 { width: 33%; text-align: justify; } +.wd40 {width: 40%; text-align: justify;} +.wd50 {width: 50%;} +.wd60 {width: 60%;} +.wd70 {width: 70%;} +.wd80 {width: 80%;} +.wd90 { width: 90%; } + +table.statement p { margin: 0; padding: 0;} + +table.alternation td { line-height: .25em; } + +table.gymnosperms td { line-height: 1em; } + + +.double-image { margin: auto 10%; } + +.pagenum { /* uncomment the next line for invisible page numbers */ + /* visibility: hidden; */ + position: absolute; + left: 92%; + color: #A9A9A9; + font-size: small; + text-align: right; + font-style: normal; + font-weight: normal; + font-variant: normal; + text-indent: 0; +} /* page numbers */ + +.blockquot { + margin: auto 0; + font-size: 90% +} + +.bb {border-bottom: 1px solid;} +.bl {border-left: 1px solid;} +.bt {border-top: 1px solid;} + +.center {text-align: center; text-indent: 0;} +.right {text-align: right;} +.smcap {font-variant: small-caps;} +.allsmcap {font-variant: small-caps; text-transform: lowercase;} + +.gesperrt +{ + letter-spacing: 0.2em; + margin-right: -0.2em; +} + +em.gesperrt +{ + font-style: normal; +} + +.caption, .captionx {font-weight: normal; font-size: 70%;} +.captionx {font-size: 70%;} + +figcaption p { text-align: justify; text-indent: 1em; font-size: 80%; } + +/* Images */ + +img { + max-width: 100%; + height: auto; +} +img.w100 {width: 100%;} + + +.figcenter { + margin: 1em auto; + text-align: center; + page-break-inside: avoid; + max-width: 100%; +} + +.figleft { + float: left; + clear: left; + margin-left: 0; + margin-bottom: .5em; + margin-top: 0; + margin-right: 1em; + padding: 0; + text-align: center; + page-break-inside: avoid; + max-width: 100%; +} +/* comment out next line and uncomment the following one for floating figleft on ebookmaker output */ +/* .x-ebookmaker .figleft {float: none; text-align: center; margin-right: 0;} */ +.x-ebookmaker .figleft {float: left;} + +.figright { + float: right; + clear: right; + margin-left: 1em; + margin-bottom: .5em; + margin-top: 0; + margin-right: 0; + padding: 0; + text-align: center; + page-break-inside: avoid; + max-width: 100%; +} +/* comment out next line and uncomment the following one for floating figright on ebookmaker output */ +/* .x-ebookmaker .figright {float: none; text-align: center; margin-left: 0;} */ +.x-ebookmaker .figright {float: right;} + +/* Footnotes */ +.footnote {margin-left: 10%; margin-right: 10%; font-size: 0.9em;} + +.footnote .label {position: absolute; right: 84%; text-align: right;} + +.footnote p { text-indent: 0; } + +.fnanchor { + vertical-align: super; + font-size: .8em; + text-decoration: + none; +} + +.vat { vertical-align: top; } +.vab { vertical-align: bottom; } +.vac { vertical-align: middle; } + + +/* Transcriber's notes */ +.transnote {background-color: #E6E6FA; + color: black; + font-size:small; + padding: 1em 1em 2em 1em; + margin-bottom:5em; + font-family:sans-serif, serif; +} + +.ws1 { word-spacing: .3em } +.pr1 { padding-right: 1em; } +.pm0 { margin: 0; padding: 0; } +.pmtb0 { margin: 0 auto; padding: 0; } +.mth { margin-top: .5em; } + +/* Illustration classes */ +.illowp10 {width: 10%;} +.illowp15 {width: 15%;} +.illowp20 {width: 20%;} +.illowp25 {width: 25%;} +.illowp30 {width: 30%;} +.illowp40 {width: 40%;} +.illowp45 {width: 45%;} +.illowp50 {width: 50%;} +.illowp60 {width: 60%;} +.illowp70 {width: 70%;} +.illowp75 {width: 75%;} +.illowp80 {width: 80%;} +.illowp90 {width: 90%;} +.illowp100 {width: 100%;} +.illowp35 {width: 35%;} +.illowp31 {width: 31%;} +.illowp76 {width: 76%;} +.illowp77 {width: 77%;} +.illowp34 {width: 34%;} +.illowp64 {width: 64%;} +.illowp55 {width: 55%;} +.illowp52 {width: 52%;} +.illowp56 {width: 56%;} +.illowp51 {width: 51%;} +.illowp54 {width: 54%;} +.illowp48 {width: 48%;} +.illowp29 {width: 29%;} +.illowp95 {width: 95%;} +.illowp43 {width: 43%;} +.illowp82 {width: 82%;} +.illowp74 {width: 74%;} +.illowp85 {width: 85%;} + </style> +</head> +<body> +<div style='text-align:center'>*** START OF THE PROJECT GUTENBERG EBOOK 78430 ***</div> + +<div class="transnote"> +<p>TRANSCRIBER’S NOTE</p> + +<p>Some minor changes to the text are noted at the end of the book.</p> +</div> + +<figure class="figcenter illowp60" id="cover" style="max-width: 112.5em;"> + <img class="w100" src="images/cover.jpg" alt="Book Cover"> +</figure> + +<hr class="chap x-ebookmaker-drop"> +<div class="chapter"></div> + +<h1> +<span class="fs120">A PRACTICAL COURSE IN<br> +BOTANY</span></h1> +<br> + +<p class="center"> +<span class="fs80">WITH ESPECIAL REFERENCE TO ITS BEARINGS ON</span><br> +<br> +<span class="fs120">AGRICULTURE, ECONOMICS, AND SANITATION</span><br> +<br> +<br> +<span class="fs80">BY</span><br> +<br> +<span class="fs120">E. F. ANDREWS</span><br> +<span class="fs60">AUTHOR OF “BOTANY ALL THE YEAR ROUND”</span><br> +<br> +<br> +<span class="fs80">WITH EDITORIAL REVISION BY</span><br> +<br> +<span class="fs100">FRANCIS E. LLOYD</span><br> +<br> +<span class="fs80">MACDONALD PROFESSOR OF BOTANY, McGILL UNIVERSITY,<br> +FORMERLY OF ALABAMA POLYTECHNIC INSTITUTE</span><br> +</p> + +<figure class="figcenter illowp75" id="i_001colophon" style="max-width: 6.1875em;"> + <img class="w100" src="images/i_001colophon.jpg" alt=""> +</figure><br> + + +<p class="center"> +<span class="fs80">NEW YORK ⁘ CINCINNATI ⁘ CHICAGO</span><br> +<span class="fs120 gesperrt ws1">AMERICAN BOOK COMPANY</span><br> +</p> + +<hr class="chap x-ebookmaker-drop"> + + +<div class="chapter"> +<p class="center"> +<span class="smcap fs80">Copyright, 1911, by<br> +E. F. ANDREWS.</span><br> +<br> +<span class="smcap">Entered at Stationers’ Hall, London.</span></p> +<hr class="r5"> +<p class="center"> +<span class="smcap fs60">ANDREW’S PR. BOTANY.<br> +W. P. 7</span><br> +</p> +</div> + + +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_iii">[Pg iii]</span></p> + +<h2 class="nobreak" id="PREFACE">PREFACE</h2> +</div> + + +<p>In preparing the present volume, the aim of the writer has +been to meet all the college entrance requirements and at the +same time to bring the study of botany into closer touch with +the practical business of life by stressing its relations with +agriculture, economics, and, in certain of its aspects, with sanitation. +While technical language has been avoided so far +as the requirements of scientific accuracy will permit, the +student is not encouraged to shirk the use of necessary botanical +terms, out of a mere superstitious fear of words because +they happen to be a little new or unfamiliar. Such a practice +not only leads to careless and inaccurate modes of expression, +but tends to foster a slovenly habit of mind, and in the long run +causes the waste of more time and labor in the search after +roundabout, and often misleading, substitutes, than it would +require to master the proper use of a few new words and +phrases.</p> + +<p>In the choice of materials for experiment and illustration, +the endeavor has been to call for such only as are familiar and +easily obtained. The specimens for flower dissection have been +selected mainly from common cultivated kinds, because their +wide distribution makes them easy to obtain everywhere, while +in cities and large towns they are practically the only specimens +available. Another important consideration has been the desire +to spare our native wild flowers, or at least not to hasten the +extinction with which they are threatened by the ravages of Sunday +excursionists and summer tourists, to whose unthinking, +but none the less destructive, incursions, the automobile has laid +open the most secret haunts of nature. The influence of the +public school teacher, and more especially the teacher of botany, +is the most potent factor from which we can hope for aid in +putting a stop to the relentless persecution that has practically +exterminated many of our choicest wild plants and is fast<span class="pagenum" id="Page_iv">[Pg iv]</span> +reducing the civilized world to a depressing monotony of +weediness and artificiality. Except for purely systematic and +anatomical work, flowers can be studied to better purpose in +their living, active state than as dead subjects for dissection; +and the best way to show our interest in them, or to get the +most rational enjoyment out of them, is not, as a general thing, +to cut their heads off and throw them away to wither and die +by the roadside. The teacher, by instilling into the minds of +the rising generation a reverence for plant life, may do a great +deal to aid in the conservation of one of our chief national assets +for the gratification of the higher esthetic instincts. The fruits +and flowers of cultivation do not stand in the same need of protection, +since they are produced solely with a view to the use +and pleasure of man, and their propagation is provided for to +meet all his demands.</p> + +<p>To avoid too frequent interruptions of the subject matter, +the experiments are grouped together at the beginning or end +of the sections to which they belong, according as they are +intended to explain what is coming, or to illustrate what has +gone before. A few exceptions are made in cases where the +experiment is such an integral part of the subject that it would +be meaningless if separated from the context. Under no +circumstances should those capable of being performed in the +schoolroom be omitted, as much of the information which the +book is intended to give is conveyed by their means. For this +reason, and also because the aim of the book is to present the +science from a practical rather than from an academic point of +view, the experiments outlined are for the most part of a simple, +practical nature, such as can be performed by the pupils themselves +with a moderate expenditure of ingenuity and money. +The experience of the writer has been that for the average boy +or girl who wishes to get a good general knowledge of the +subject, but does not propose to become a specialist in botany, +the best results are often obtained by the use of the simplest +and most familiar appliances, as in this way attention is not +distracted from the experiment itself to the unfamiliar apparatus +for making it. In saying this, it is not meant to underrate<span class="pagenum" id="Page_v">[Pg v]</span> +the value of a complete laboratory equipment, but merely +to emphasize the fact that the lack of it, while a disadvantage, +need not be an insuperable bar to the successful teaching of +botany. It is, of course, taken for granted that in schools provided +with a suitable laboratory outfit, teachers will be prepared +to supplement or to replace the exercises here outlined +with such others as in their judgment the subject may demand. +There are as many ideals in teaching as there are teachers, and +the most that a textbook can do is to present a working model +which every teacher is free to modify in accordance with his +or her own method.</p> + +<p>The writer takes pleasure in acknowledging here the many +obligations due to Professor Francis E. Lloyd, of the Botanical +Department of the Alabama Polytechnic Institute, at Auburn, +Ala., for his valuable aid in the revision of the manuscript, for +the highly interesting series of illustrations relating to phototropic +movements, and for advice and information on points +demanding expert knowledge which have contributed very materially +to whatever merit this volume may possess.</p> + +<p>Other members of the Auburn faculty to whom the author +feels especially indebted are Mr. C. S. Ridgeway, assistant in the +Botanical Department, Professor J. E. Duggar, of the Agricultural +Department, and Dr. B. B. Ross and Professor C. W. +Williamson of the Department of Chemistry. Acknowledgments +are due also to Professor George Wood of the Boys’ High +School, Brooklyn, for suggestions which have been of great +assistance in the preparation of this work; to Professor W. R. +Dodson, of the University of Louisiana, for illustrative material +furnished, and to Professor William Trelease for the loan of +original material used in reproducing the beautiful cuts from +the Reports of the Missouri Botanical Garden, credit for which +is given in the proper place.</p> + +<p>For original photographs and drawings by the author, and +familiar selections from well-known works, which can be generally +recognized, it has not been thought necessary to give +special credit.</p> + +<p class="right"> +E. F. ANDREWS.<br> +</p> + +<div class="blockquot"> + +<p><span class="smcap">Auburn, Alabama.</span></p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_vi">[Pg vi]</span></p> + +<h2 class="nobreak" id="FULL-PAGE_ILLUSTRATIONS">FULL-PAGE ILLUSTRATIONS</h2> +</div> + + +<table class="autotable fs90 wd70"> +<tr> +<td class="tdl fs80">PLATE</td> +<td class="tdr fs80">PAGE</td> +</tr> +<tr> +<td class="tdl smcap"> 1. A grove of live oaks near Savannah, Georgia</td> +<td class="tdr"><i><a href="#i_010">Frontispiece</a></i></td> +</tr> +</table> + +<table class="autotable fs90 wd70 smcap"> +<tr> +<td class="tdl"> 2. Carrying water over the Mississippi levee by siphon to irrigate rice fields</td> +<td class="tdr"><a href="#Page_8">8</a></td> +</tr> +<tr> +<td class="tdl"> 3. Aërial roots of a Mexican strangling fig</td> +<td class="tdr"><a href="#Page_73">73</a></td> +</tr> +<tr> +<td class="tdl"> 4. A forest of bamboo</td> +<td class="tdr"><a href="#Page_99">99</a></td> +</tr> +<tr> +<td class="tdl"> 5. A group of conifers</td> +<td class="tdr"><a href="#Page_108">108</a></td> +</tr> +<tr> +<td class="tdl"> 6. A white oak, showing the great spread of branches</td> +<td class="tdr"><a href="#Page_117">117</a></td> +</tr> +<tr> +<td class="tdl"> 7. A timber tree spoiled by standing too much alone</td> +<td class="tdr"><a href="#Page_125">125</a></td> +</tr> +<tr> +<td class="tdl"> 8. An American elm, illustrating deliquescent growth</td> +<td class="tdr"><a href="#Page_130">130</a></td> +</tr> +<tr> +<td class="tdl"> 9. Vegetation of a moist, shady ravine</td> +<td class="tdr"><a href="#Page_151">151</a></td> +</tr> +<tr> +<td class="tdl">10. A mosaic of moonseed leaves</td> +<td class="tdr"><a href="#Page_179">179</a></td> +</tr> +<tr> +<td class="tdl">11. Hybrid between a red and a white carnation</td> +<td class="tdr"><a href="#Page_227">227</a></td> +</tr> +<tr> +<td class="tdl">12. Gooseberries, showing improvement by selection</td> +<td class="tdr"><a href="#Page_251">251</a></td> +</tr> +<tr> +<td class="tdl">13. The effects of irrigation</td> +<td class="tdr"><a href="#Page_272">272</a></td> +</tr> +<tr> +<td class="tdl">14. A xerophyte formation of yuccas and switch plants</td> +<td class="tdr"><a href="#Page_282">282</a></td> +</tr> +<tr> +<td class="tdl">15. A giant tulip tree of the South Atlantic forest region</td> +<td class="tdr"><a href="#Page_293">293</a></td> +</tr> +</table> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_vii">[Pg vii]</span></p> + +<h2 class="nobreak" id="CONTENTS">CONTENTS</h2> +</div> + +<table class="autotable fs90 smcap"> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_I">CHAPTER I</a>. THE SEED</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdr fs80" colspan="2">PAGE</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_I_I">The Storage of Food in Seeds</a></td> +<td class="tdr">1</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_I_II">Some Physiological Properties of Seeds</a></td> +<td class="tdr">10</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_I_III">Types of Seeds</a></td> +<td class="tdr">12</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_I_IV">Seed Dispersal</a></td> +<td class="tdr">21</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_I_FIELD">Field Work</a></td> +<td class="tdr">28</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_II">CHAPTER II</a>. GERMINATION AND GROWTH</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_II_I">Processes accompanying Germination</a></td> +<td class="tdr">29</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_II_II">Conditions of Germination</a></td> +<td class="tdr">33</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_II_III">Development of the Seedling</a></td> +<td class="tdr">40</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_II_IV">Growth</a></td> +<td class="tdr">47</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_II_FIELD">Field Work</a></td> +<td class="tdr">52</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_III">CHAPTER III</a>. THE ROOT</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_III_I">Osmosis and the Action of the Cell</a></td> +<td class="tdr">53</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_III_II">Mineral Nutriments absorbed by Plants</a></td> +<td class="tdr">58</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_III_III">Structure of the Root</a></td> +<td class="tdr">61</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_III_IV">The Work of Roots</a></td> +<td class="tdr">65</td> +</tr> +<tr> +<td class="tdr">V.</td> +<td class="tdl"><a href="#CH_III_V">Different Forms of Roots</a></td> +<td class="tdr">72</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_III_FIELD">Field Work</a></td> +<td class="tdr">80</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_IV">CHAPTER IV</a>. THE STEM</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_IV_I">Forms and Growth of Stems</a></td> +<td class="tdr">81</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_IV_II">Modifications of the Stem</a></td> +<td class="tdr">88</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_IV_III">Stem Structure</a></td> +<td class="tdr"></td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_IV_III_A">A. Monocotyls</a></td> +<td class="tdr">96</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_IV_III_B">B. Herbaceous Dicotyls</a></td> +<td class="tdr">102</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_IV_III_C">C. Woody Stemmed Dicotyls</a></td> +<td class="tdr">107<span class="pagenum" id="Page_viii">[Pg viii]</span></td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_IV_IV">The Work of Stems</a></td> +<td class="tdr">112</td> +</tr> +<tr> +<td class="tdr">V.</td> +<td class="tdl"><a href="#CH_IV_V">Wood Structure in its Relation to Industrial Uses</a></td> +<td class="tdr">118</td> +</tr> +<tr> +<td class="tdr">VI.</td> +<td class="tdl"><a href="#CH_IV_VI">Forestry</a></td> +<td class="tdr">124</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_IV_FIELD">Field Work</a></td> +<td class="tdr">128</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_V">CHAPTER V</a>. BUDS AND BRANCHES</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_V_I">Modes of Branching</a></td> +<td class="tdr">131</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_V_II">Buds</a></td> +<td class="tdr">138</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_V_III">The Branching of Flower Stems</a></td> +<td class="tdr">141</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_V_FIELD">Field Work</a></td> +<td class="tdr">145</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_VI">CHAPTER VI</a>. THE LEAF</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_VI_I">The Typical Leaf and its Parts</a></td> +<td class="tdr">147</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_VI_II">The Veining and Lobing of Leaves</a></td> +<td class="tdr">154</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_VI_III">Transpiration</a></td> +<td class="tdr">160</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_VI_IV">Anatomy of the Leaf</a></td> +<td class="tdr">164</td> +</tr> +<tr> +<td class="tdr">V.</td> +<td class="tdl"><a href="#CH_VI_V">Food Making</a></td> +<td class="tdr">168</td> +</tr> +<tr> +<td class="tdr">VI.</td> +<td class="tdl"><a href="#CH_VI_VI">The Leaf an Organ of Respiration</a></td> +<td class="tdr">174</td> +</tr> +<tr> +<td class="tdr">VII.</td> +<td class="tdl"><a href="#CH_VI_VII">The Adjustment of Leaves to External Relations</a></td> +<td class="tdr">177</td> +</tr> +<tr> +<td class="tdr">VIII.</td> +<td class="tdl"><a href="#CH_VI_VIII">Modified Leaves</a></td> +<td class="tdr">189</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_VI_FIELD">Field Work</a></td> +<td class="tdr">194</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_VII">CHAPTER VII</a>. THE FLOWER</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_VII_I">Dissection of Types with Superior Ovary</a></td> +<td class="tdr">196</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_VII_II">Dissection of Types with Inferior Ovary</a></td> +<td class="tdr">204</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_VII_III">Study of a Composite Flower</a></td> +<td class="tdr">210</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_VII_IV">Specialized Flowers</a></td> +<td class="tdr">214</td> +</tr> +<tr> +<td class="tdr">V.</td> +<td class="tdl"><a href="#CH_VII_V">Function and Work of the Flower</a></td> +<td class="tdr">219</td> +</tr> +<tr> +<td class="tdr">VI.</td> +<td class="tdl"><a href="#CH_VII_VI">Hybridization</a></td> +<td class="tdr">223</td> +</tr> +<tr> +<td class="tdr">VII.</td> +<td class="tdl"><a href="#CH_VII_VII">Plant Breeding</a></td> +<td class="tdr">230</td> +</tr> +<tr> +<td class="tdr">VIII.</td> +<td class="tdl"><a href="#CH_VII_VIII">Ecology of the Flower</a></td> +<td class="tdr"></td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_VII_VIII_A">A. The Prevention of Self-pollination</a></td> +<td class="tdr">235</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_VII_VIII_B">B. Wind Pollination</a></td> +<td class="tdr">239</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_VII_VIII_C">C. Insect Pollination</a></td> +<td class="tdr">241</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_VII_VIII_D">D. Protective Adaptation</a></td> +<td class="tdr">245</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_VII_FIELD">Field Work</a></td> +<td class="tdr">249<span class="pagenum" id="Page_ix">[Pg ix]</span></td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_VIII">CHAPTER VIII</a>. FRUITS</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_VIII_I">Horticultural and Botanical Fruits</a></td> +<td class="tdr">250</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_VIII_II">Fleshy Fruits</a></td> +<td class="tdr">255</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_VIII_III">Dry Fruits</a></td> +<td class="tdr">260</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_VIII_IV">Accessory, Aggregate, and Multiple Fruits</a></td> +<td class="tdr">265</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_VIII_FIELD">Field Work</a></td> +<td class="tdr">269</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_IX">CHAPTER IX</a>. THE RESPONSE OF THE PLANT TO ITS SURROUNDINGS</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_IX_I">Ecological Factors</a></td> +<td class="tdr">271</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_IX_II">Plant Associations</a></td> +<td class="tdr">277</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_IX_III">Zones of Vegetation</a></td> +<td class="tdr">288</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_IX_FIELD">Field Work</a></td> +<td class="tdr">294</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#CH_X">CHAPTER X</a>. CRYPTOGAMS</td> +</tr> +<tr> +<td class="tdr">I.</td> +<td class="tdl"><a href="#CH_X_I">Their Place in Nature</a></td> +<td class="tdr">296</td> +</tr> +<tr> +<td class="tdr">II.</td> +<td class="tdl"><a href="#CH_X_II">Algæ</a></td> +<td class="tdr">299</td> +</tr> +<tr> +<td class="tdr">III.</td> +<td class="tdl"><a href="#CH_X_III">Fungi</a></td> +<td class="tdr">303</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_X_III_A">A. Bacteria</a></td> +<td class="tdr">306</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_X_III_B">B. Yeasts</a></td> +<td class="tdr">314</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_X_III_C">C. Rusts</a></td> +<td class="tdr">317</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl pad2"><a href="#CH_X_III_D">D. Mushrooms</a></td> +<td class="tdr">323</td> +</tr> +<tr> +<td class="tdr">IV.</td> +<td class="tdl"><a href="#CH_X_IV">Lichens</a></td> +<td class="tdr">329</td> +</tr> +<tr> +<td class="tdr">V.</td> +<td class="tdl"><a href="#CH_X_V">Liverworts</a></td> +<td class="tdr">334</td> +</tr> +<tr> +<td class="tdr">VI.</td> +<td class="tdl"><a href="#CH_X_VI">Mosses</a></td> +<td class="tdr">341</td> +</tr> +<tr> +<td class="tdr">VII.</td> +<td class="tdl"><a href="#CH_X_VII">Fern Plants</a></td> +<td class="tdr">344</td> +</tr> +<tr> +<td class="tdr">VIII.</td> +<td class="tdl"><a href="#CH_X_VIII">The Relation between Cryptogams and Seed Plants</a></td> +<td class="tdr">354</td> +</tr> +<tr> +<td class="tdr">IX.</td> +<td class="tdl"><a href="#CH_X_IX">The Course of Plant Evolution</a></td> +<td class="tdr">359</td> +</tr> +<tr> +<td class="tdr"></td> +<td class="tdl"><a href="#CH_X_FIELD">Field Work</a></td> +<td class="tdr">362</td> +</tr> +<tr> +<td class="tdc pad-chap" colspan="3"><a href="#APPENDIX">APPENDIX</a></td> +</tr> +<tr> +<td class="tdr">1.</td> +<td class="tdl"><a href="#APP_1">Systematic Botany</a></td> +<td class="tdr">364</td> +</tr> +<tr> +<td class="tdr">2.</td> +<td class="tdl"><a href="#APP_2">Weights, Measures, and Temperatures</a></td> +<td class="tdr">367</td> +</tr> +</table> + +<p><span class="pagenum" id="Page_x">[Pg x]</span></p> + +<figure class="figcenter illowp100" id="i_010" style="max-width: 100.25em;"> + <img class="w100" src="images/i_010.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Plate 1.</span>—Live oaks covered with Spanish moss (<i>Tillandsia</i>).</p></figcaption> +</figure> + +<div class="chapter"> +<p><span class="pagenum" id="Page_1">[Pg 1]</span></p> + +<h2 class="nobreak" id="CH_I">CHAPTER I. THE SEED</h2> +</div> + + +<h3 id="CH_I_I">I. THE STORAGE OF FOOD IN SEEDS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—In addition to the four food tests described in <a href="#exp-1">Exps. +1-6</a>, there should be provided some raw starch, a solution of grape +sugar, the white of a hard-boiled egg, and any fatty substance, such +as lard or oil. For Exps. 8 and 9, a little diastase solution will be necessary. +“Taka” diastase, made from rice acted upon by a fungus, can +be obtained for a trifle at almost any drug store.</p> + +<p><span class="smcap">Living material.</span>—Grains of corn and wheat, and seeds of some +kind of bean, the larger the better. The “horse bean” (<i>Vicia faba</i>), if +it can be obtained, makes an excellent object for study, as the cells are +so large that they can be seen with the naked eye. For showing the +presence of proteins (aleurone grains) and oily matter, use thin cross sections +through the kernel of a castor bean or a Brazil nut. Specimens +for the study of the individual cell will be found in the hairs growing on +squash seedlings, in the epidermis of one of the inner coats of an onion, in +the roots of oat or radish seedlings, or in the section of a young corn root.</p> + +<p>A compound microscope will be required for this study.</p> +</div> + +<p id="p-1"><b>1. The economic importance of seeds.</b>—As a source of +food to both man and the lower animals, the importance of +seeds can hardly be overrated. All the flour, meal, rice, +hominy, and other breadstuffs sold in the market come from +them, to say nothing of the fleece from the cotton seed that +clothes the greater part of the world, besides furnishing a +substitute for lard and an important food for cattle. The +oils and fats stored in nuts are also to be taken into account, +the peanut alone yielding the greater part of the so-called +olive oil of commerce. Since the value of our farm crops +depends largely upon the kind and quantity of these substances +furnished by them, it is worth our while, as a matter +of economic as well as scientific interest, to learn something +about the nature of the different foods contained in plants.</p> + +<p><span class="pagenum" id="Page_2">[Pg 2]</span></p> + +<figure class="figcenter illowp100" id="i_012" style="max-width: 50em;"> + <img class="w100" src="images/i_012.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 1-3.</span>—The world’s three most important food grains (magnified): 1, section +of a rice grain; <i>a</i>, cuticle; <i>b</i>, aleurone, or protein layer; <i>c</i>, starch cells; <i>d</i>, germ; +2, section of a wheat grain; <i>k</i>, germ; <i>s</i>, starch; <i>a</i>, gluten; <i>t</i>, <i>t</i>, <i>t</i>, layers of the seed +coat; 3, section of a grain of corn; <i>c</i>, husk; <i>e</i>, aleurone layer containing proteins; +<i>eg</i>, yellowish, horny endosperm, containing proteins and starch; <i>ew</i>, lighter starchy +endosperm: the darker part below is rich in oil and proteins, and contains the <i>embryo</i>, +consisting of the absorbing organ, or <i>cotyledon</i>, <i>sc</i>; the rudimentary bud, <i>s</i>; and +the root, <i>w</i>. (1, from Circular 77, La. Exp. Station; 2, from Francé; 3, from Sachs.)</p></figcaption> +</figure> + +<p id="p-2"><b>2. Why food is stored in seeds.</b>—The one purpose +for which plants produce their seed is to give rise to a new +generation and so carry on the life of the species. The +seed is the nursery, so to speak, in which the germ destined +to produce a new plant +is sheltered until it is +ready to begin an independent +existence. But +the young plant, like +the young animal, is +incapable of providing +for itself at first, and +would die unless it received +nourishment from +the mother plant until +it has formed roots and +leaves so that it can +manufacture food for<span class="pagenum" id="Page_3">[Pg 3]</span> +itself. Plants in general require very much the same food +that animals do, and they have the power, which animals +have not, of manufacturing it out of the crude materials contained +in the soil water and in the air. Such of these foods +as are not needed for immediate consumption, they store up +to serve as a provision for the young shoot when the seed +begins to germinate.</p> + +<figure class="figcenter illowp60" id="i_012a" style="max-width: 25em;"> + <img class="w100" src="images/i_012a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 4-7.</span>—Sections of corn grains showing +different qualities of food contents: 4, 5, small +germ and large proportion of horny part, showing +high protein; 6, 7, large germ and smaller proportion +of horny part, showing high oil content.</p></figcaption> +</figure> + +<p id="p-3"><b>3. Food substances contained in seeds.</b>—There are four +principal classes of food stored in seeds: <em>sugars</em>, <em>starches</em>, <em>oils</em>, +and <em>proteins</em>. The first are held in solution and can be +detected, if in sufficient quantity, by the taste. The most +important varieties of this group are cane and grape sugar, +the latter occurring most abundantly in fruits, the former in +roots and stems. Oil usually occurs in the form of globules. +It is very abundant in some seeds, <i>e.g.</i> flax, castor bean, and +Brazil nut. In the corn grain it is found in the part constituting +the germ, or embryo (<a href="#i_012a">Figs. 6, 7</a>). Starches and proteins +occur in the form of small granules, which have specific +shapes in different plants (<a href="#i_013">Figs. 8, 9</a>). Those containing proteins +are called <em>aleurone</em> grains, and are, as a rule, smaller +than the starch grains with which they are intermixed in the +bean and some other seeds. In wheat, corn, rice, and most +grains they form a layer just inside the husk, as shown in +<a href="#i_014">Fig. 10</a>. This is the reason why polished rice and finely +bolted flour are less nutritious +than the darker +kinds, from which this +valuable food substance +has not been removed. +The two most familiar +kinds of proteins are the +<em>albumins</em>, of which the +white of an egg is +a well-known example, +and the <em>glutins</em>, which give to the dough of wheat flour and +oatmeal their peculiar gummy or “glutinous” structure.</p> + +<figure class="figcenter illowp60" id="i_013" style="max-width: 25em;"> + <img class="w100" src="images/i_013.jpg" alt=""> + <figcaption><p id="fig-8"><span class="smcap">Figs. 8-9.</span>—Different forms of starch grains: +8, rice; 9, wheat.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_4">[Pg 4]</span></p> + +<p id="p-4"><b>4. Organic foods.</b>—These four substances, starch, sugar, +fats, and proteins, with some others of less frequent occurrence, +are called <em>organic +foods</em>, because they are produced, +in a state of nature, +only through the action of +organized living bodies, or, +more strictly speaking, of +living vegetable bodies.</p> + +<figure class="figcenter illowp50" id="i_014" style="max-width: 25em;"> + <img class="w100" src="images/i_014.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 10.</span>—Transverse section near the +outside of a wheat grain: <i>e</i>, the husk; <i>a</i>, cells +containing protein granules; <i>s</i>, starch cells +(<i>after</i> Tschirch).</p></figcaption> +</figure> + +<p id="p-5"><b>5. Our dependence upon +plants.</b>—While the animal +organism can digest and +assimilate these substances +after they have been formed +by plants, it has no power +to manufacture them for +itself, and, so far as we know at present, is wholly dependent +upon the vegetable world for these necessaries of life. +In one sense the whole animal kingdom may be said to be +parasitic on plants. The wolf that eats a lamb is getting +his food indirectly from the grains and grasses consumed +by its victim, and the lion that devours the wolf that ate +the lamb is only one step further removed from a vegetable +diet.</p> + +<p id="p-6"><b>6. The vegetable cell.</b>—If you will break open a well-soaked +horse bean and examine the contents with a lens, you +will see that they are composed of small oval or roundish +granules packed together like stones in a piece of masonry. +These little bodies, called <em>cells</em>, are the ultimate units out +of which all animal and vegetable structures are built up, as +a wall is built of bricks and stones. They differ very much +from bricks and stones, however, in that they are, or have +been, living structures with their periods of growth, activity, +decline, and death, just like other living matter, as will be +seen by and by, when we come to look more particularly +into their life history. They consist usually of an inclosing<span class="pagenum" id="Page_5">[Pg 5]</span> +membrane which contains a living substance called +<em>protoplasm</em>. This is the essential part of the cell, and, so +far as we know at present, the physical basis of all life. +Cells are commonly more or less rounded in shape, though +they take different forms according to the purpose they +serve. Sometimes, as in the fibers of cotton and the down +of young leaves, they are long and hairlike; when closely +packed, they often become angular by pressure, like those +shown in <a href="#i_014">Figs. 10</a>, <a href="#i_015">11</a>. The cells composing the thick body of +the bean are for the most part starch and other substances +stored up for food, which render observation difficult. It +will, therefore, be better to choose for a study of the individual +cell some kind that will show the essential parts more +distinctly.</p> + +<figure class="figright illowp30" id="i_015" style="max-width: 25em;"> + <img class="w100" src="images/i_015.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 11</span>—Typical cells: +<i>n</i>, nucleus; <i>p</i>, protoplasm; +<i>w</i>, cell wall; <i>s</i>, sap.</p></figcaption> +</figure> + +<p id="p-7"><b>7. Microscopic examination of a cell.</b>—Place under a high +power of the microscope a portion of fresh skin from one of +the inside scales of an onion, or a piece +of the root tip of a very young corn or oat +seedling, and fix your attention on one of +the individual cells. Notice (1) the cell +wall or inclosing membrane, <i>w</i> (<a href="#i_015">Fig. 11</a>); +(2) the protoplasm, <i>p</i>, which may be +recognized by its granular appearance; +(3) the <em>nucleus</em>, <i>n</i>; and (4) the cell sap, <i>s</i>. +In very young cells the protoplasm will +be seen to fill most of the interior; but +in mature ones, like the large one on the +right of the figure, it forms a thin lining +around the wall, with the nucleus on one side, while the cell +sap, composed of various substances in solution, occupies the +central portion. Though there is generally an inclosing wall, +this is not essential, its office being to give strength and mechanical +support by holding the contents together, as an +India-rubber bag holds water. It is the turgidity of the cell, +when distended with liquid, that gives firmness to herbaceous +plants and the tender parts of woody ones. This<span class="pagenum" id="Page_6">[Pg 6]</span> +may be illustrated by observing the difference between a +rubber bag when quite full and when only half full of water, +or a football when partially and when fully inflated. In +its simplest form, however, the cell is a mere particle of +protoplasm, which has one part, constituting the nucleus, +a little more dense in appearance than the rest, but this +kind is not common in vegetable structures.</p> + +<p id="p-8"><b>8. How food substances get into the cells.</b>—As there +are no openings in the cell walls, the only way substances +can get into a cell or out of it is by soaking through the +inclosing membrane, as will be explained in a later chapter. +Since starch, oil, and proteins, the most important foods +stored in seeds, are none of them soluble in the cell sap, it is +clear that they could not have got into the cells in their +present state, but must have undergone some change by +which they were rendered capable of passing through the +cell wall.</p> + +<p id="p-9"><b>9. Digestion.</b>—The process by which this change is +brought about is known as <em>digestion</em>, from its similarity to +the same function in animals. Not only are foods, in the +state in which we find them stored in the seed, incapable +of passing through the cell wall, but the protoplasm, the +living part of the cell, has no power to assimilate and to +utilize these substances as food until they have been reduced +to a soluble form in which they can be diffused freely +from cell to cell through any part of the plant. By <em>diffusion</em> +is meant the gradual spread of soluble substances through +the containing medium, as when a lump of sugar or salt, +dropped into a glass of water, dissolves and slowly diffuses +through the contents, imparting a sweet or salty taste to the +whole.</p> + +<figure class="figright illowp50" id="i_017" style="max-width: 25em;"> + <img class="w100" src="images/i_017.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 12.</span>—Starch grains of wheat in +different stages of disintegration under the +action of a ferment (diastase), accompanying +germination: <i>a</i>, slightly corroded; <i>b</i>, <i>c</i>, +and <i>d</i>, more advanced stages of decomposition.</p></figcaption> +</figure> + +<p>During the process of digestion the different kinds of +food are acted upon and made soluble by certain chemical +ferments, which are secreted in plants for the purpose. The +digestion of starch, the most abundant of plant foods, is +effected by diastase, a common ferment obtained from germinating<span class="pagenum" id="Page_7">[Pg 7]</span> +grains of barley, wheat, corn, rice, etc. By the +presence of diastase starch is converted into grape sugar, a +substance which is readily soluble in water, and which can +be diffused easily through the tissues of the plant to any +part where it is needed. In this way food travels from the +leaf, where it is made, to +the seed, where the sugar is +generally reconverted into +starch and stored up for +future use, though sometimes, +as in the sugar corn +and sugar pea, it remains +in part unchanged. The +kernels of this kind of corn +can be distinguished readily +from those of the ordinary +starch corn, after maturity, +by their wrinkled appearance, +owing to their greater +loss of water in drying.</p> + +<p id="p-10"><b>10. Food tests.</b>—In order +to tell whether any of +the food substances named +occur in the seeds that we are going to examine, it will be +necessary to understand a few simple tests by which their +presence may be recognized. The chemicals required can +be ordered ready for use from a druggist or may be prepared +in the laboratory as needed, according to the directions +given. Write in your notebook a brief account of each experiment +made, with the conclusions drawn from it.</p> + +<div class="blockquot"> + +<p id="exp-1"><span class="smcap">Experiment 1. To detect the presence of fats.</span>—Rub a small lump +of butter or a drop of oil on a piece of thin white paper. What is the effect?</p> + +<p id="exp-2"><span class="smcap">Experiment 2. Another test for fats.</span>—Place some macerated +alcanna root in a vessel with alcohol enough to cover it, and leave for an +hour. Add an equal bulk of water and filter. The solution will stain +fats, oils, and resins deep red.</p> +</div> + +<p><span class="pagenum" id="Page_8">[Pg 8]</span></p> + +<figure class="figcenter illowp100" id="i_018" style="max-width: 99.5625em;"> + <img class="w100" src="images/i_018.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 2.</span>—Carrying water over the Mississippi levee by siphon to irrigate rice fields. (<i>From</i> Circular of La. Exp. Station.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_9">[Pg 9]</span></p> + +<div class="blockquot"> + +<p id="exp-3"><span class="smcap">Experiment 3. To show the presence of starch.</span>—Put a drop of +iodine solution on some starch. What change of color takes place? To +make iodine solution, add to one part of iodine crystals 4 parts potassium +iodide and 95 parts water. It should be kept in the dark, as light +decomposes it. Iodine colors starch blue, protein substances light brown. +In testing for starch, the solution should be diluted till it is of a pale color, +otherwise the stain will be so deep as to appear black.</p> + +<p id="exp-4"><span class="smcap">Experiment 4. A test for proteins.</span>—Place a small quantity of +the white of an egg, diluted with water, in a clean glass and add a few +drops of nitric acid; or drop some of the acid on the white of a hard-boiled +egg. What is the effect?</p> + +<p>Nitric acid turns proteins yellow; if the color is indistinct, add a drop +of ammonia, when an orange color will ensue.</p> + +<p id="exp-5"><span class="smcap">Experiment 5. Another test for proteins.</span>—Place on the substance +to be examined a drop of a saturated solution of cane sugar and +water; add a drop of pure sulphuric acid; if proteins are present, they +will be colored red. See also <a href="#exp-3">Exp. 3</a>.</p> + +<p id="exp-6"><span class="smcap">Experiment 6. A test for grape sugar.</span>—Heat a teaspoonful of +Fehling’s Solution to the boiling point in a test tube (a common glass vial +can be used by heating gradually in water) and pour in a few drops of +grape sugar solution. Heat again and observe the color of the precipitate +that forms.</p> + +<p>Fehling’s Solution may be obtained of the druggist, or, if preferred, +it may be prepared in the laboratory as follows: (<i>a</i>) Dissolve 173 grams +of crystallized Rochelle salts and 125 grams of caustic potash in 500 cc. of +water; (<i>b</i>) dissolve 34.64 grams crystallized copper sulphate in 500 cc. +of water, and mix equal parts as needed. (For English equivalents, see +Appendix, Weights and Measures.) The two mixtures must be kept separate +till wanted for use, or prepared fresh as needed.</p> + +<p>Grape Sugar causes Fehling’s Solution to form a red precipitate.</p> + +<p id="exp-7"><span class="smcap">Experiment 7. To show the difference between sugar and +starch in regard to solubility.</span>—Mix some sugar with water and +notice how readily it dissolves. Try the same experiment with starch +and observe its different behavior.</p> + +<p id="exp-8"><span class="smcap">Experiment 8. To show how starch is disintegrated in the act +of digestion.</span>—Place a few grains of starch on a slide, add a drop or +two of diastase solution, and observe under the microscope; the starch +granules will be seen to disintegrate and melt away. Even with a hand +lens it can be seen, from the greater clearness of the liquid in comparison +with a mixture of untreated starch and water, that the grains have been +dissolved.</p> + +<p><span class="pagenum" id="Page_10">[Pg 10]</span></p> + +<p id="exp-9"><span class="smcap">Experiment 9. To show that diastase converts starch into +sugar.</span>—Make a paste of boiled starch so thin that it looks like water. +Pour a small quantity of it into each of two tubes, adding a little diastase +to one and leaving the other untreated. Keep in a warm place for twenty-four +hours, then test both tubes for starch, as directed in <a href="#exp-3">Exp. 3</a>, and note +the result. If the diastase has not acted, add a little more and watch.</p> +</div> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Name all the food and other economic products you can think of +that are derived from the seed of maize; from wheat; from flaxseed; +from cotton.</p> + +<p>2. Mention some seeds from which medicines are procured.</p> + +<p>3. Name all the seeds you can think of from which oil is obtained; +starch; some that are rich in proteins. (<a href="#exp-1">Exps. 1-5</a>.)</p> + +<p>4. Describe some of the ways in which these products are frequently +adulterated.</p> + +<p>5. If you were raising corn to sell to a starch factory, what part of +the seed would you seek to develop? If to feed stock, what part? Why, +in each case? (<a href="#p-3">3</a>; <a href="#i_012a">Figs. 4-7</a>.)</p> + +<p>6. What grain feeds more human beings than does any other?</p> + +<p>7. Name all the seeds you can think of that contain sugar in sufficient +quantity to be detected without chemical tests; that is, by tasting alone.</p> + +<p>8. Is “coal oil” a mineral or an organic substance? Explain, by +giving an account of its origin.</p> + +<p>9. What is gluten? (<a href="#p-3">3</a>.) Name some grains that are especially rich in it.</p> + +<p>10. Which of our three chief food grains is a water plant? (See <a href="#i_018">Plate +2</a>.) Which grows farthest south? Which farthest north? Which one is +of American origin?</p> +</div> + + +<h3 id="CH_I_II">II. SOME PHYSIOLOGICAL PROPERTIES OF SEEDS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Seeds of squash, pumpkin, or other melon; castor bean; +any kind of common kidney bean; grains of Indian corn.</p> + +<p><span class="smcap">Appliances.</span>—In the absence of gas, an alcohol or kerosene lamp may +be used for heating. A double boiler can easily be made by using two tin +vessels of different sizes. Partly fill the larger one with water, set in it +the smaller one with the substance to be heated, and place over a burner. +A pair of scales, a strong six-ounce bottle, wire-netting, cord, and wax +or paraffin should be provided.</p> + +<p id="exp-10"><span class="smcap">Experiment 10. Do seeds in their ordinary quiescent state +contain any water?</span>—Place a number of beans, or grains of corn or +wheat in a glass bottle, making a small perforation in the cork to allow +the air to escape, and heat gently. Does any moisture form on the glass?</p> + +<p><span class="pagenum" id="Page_11">[Pg 11]</span></p> + +<p>A better test is to weigh two or three ounces of seeds, and heat them +in a double boiler or in oil to prevent scorching. Weigh at intervals. If +there is any loss of weight, to what is it due?</p> + +<p id="exp-11"><span class="smcap">Experiment 11. Do seeds absorb water?</span>—Soak a number of +beans or grains of corn in water for 12 to 24 hours and compare with +dry ones. What difference do you notice? To what cause is it due?</p> + +<p id="exp-12"><span class="smcap">Experiment 12. How did water get into the soaked seeds?</span>—Dry +gently with a soft cloth some of the seeds used in the last experiment +and press them lightly to see if water comes out, and where. Place a number +of dry seeds of different kinds—squash, bean, castor bean, quince, +etc.—in warm water and notice whether any bubbles of air form on them +and at what point. Examine with a lens and see if this point differs in any +way from the rest of the seed cover. Does it correspond with the point +from which water exuded in the soaked seeds? Could hard seeds like +the squash, castor bean, buckeye, and Brazil nut get water readily without +an opening somewhere in the coat?</p> + +<p id="exp-13"><span class="smcap">Experiment 13. To find out whether water is absorbed +through the seed coats.</span>—Place in moist sand or sawdust two rows +of beans as nearly as possible of the same size and weight, with the eye +pressed down to the substratum in one row and turned up in the other, so +that no moisture can enter through it. In the same way arrange two +rows of castor beans with the little end down in one row and uppermost +in the other. In the last set carefully break away the spongy mass near +the tip, without injuring the parts about it. Watch and see in which +rows water is absorbed most readily. What change takes place in the +spongy masses at the tips of those castor beans on +which they were left?</p> + +<figure class="figright illowp20" id="i_021" style="max-width: 25em;"> + <img class="w100" src="images/i_021.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 13.</span>—Effect +of the expansion of +seeds due to absorption +of water.</p></figcaption> +</figure> + +<p id="exp-14"><span class="smcap">Experiment 14. Is the rate of germination +affected by the presence or absence of +openings?</span>—Seal up with wax or paraffin all the +openings of a number of air-dry peas or beans, and +leave an equal number of the same size and weight +untreated. Be careful that the sealing is absolutely +water-tight, since otherwise the experiment will +be worthless. Plant both sets and keep under like +conditions of soil, temperature, and moisture. Do +you see any difference in the rate of germination of +the two sets?</p> + +<p id="exp-15"><span class="smcap">Experiment 15. Do seeds exert force in +absorbing water?</span>—Fill a common six-ounce bottle +as full as it will hold with dry peas, beans, or<span class="pagenum" id="Page_12">[Pg 12]</span> +grains of corn; then pour in water till the bottle is full. Tie a piece of +wire-netting or stout sackcloth over the top to keep the seeds from being +forced out. Bind both the neck and the body of the bottle tightly with +strong cords encircling it in both a horizontal and vertical direction, and +place under water in a moderately warm temperature. Watch for results.</p> + +<p id="exp-16"><span class="smcap">Experiment 16. Is the force exerted in the last experiment +a merely mechanical one, like the bursting of a water pipe, or +is it physiological and thus dependent on the fact that the +seeds are alive?</span>—To answer this question try <a href="#exp-15">Exp. 15</a> with seeds +that have been killed by heat or by soaking in formalin.</p> +</div> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Will a pound of pop corn weigh as much after being popped as before? +(<a href="#exp-10">Exp. 10</a>.)</p> + +<p>2. What causes the difference, if there is any? (<a href="#exp-10">Exp. 10</a>.)</p> + +<p>3. Does the tuft of downy hairs at the tip of wheat and oat grains +influence their water supply? The spongy covering of black walnuts and +almonds? The pithy inside layers of pecans and English walnuts? +(<a href="#exp-12">Exps. 12</a>, <a href="#exp-13">13</a>.)</p> + +<p>4. Why will seeds, as a general thing, germinate more readily after +being soaked? (<a href="#exp-11">Exps. 11</a>, <a href="#exp-14">14</a>, <a href="#exp-16">16</a>.)</p> +</div> + + +<h3 id="CH_I_III">III. TYPES OF SEEDS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Dry and soaked grains of corn, wheat, or oats; bean, +squash, castor bean, and pine seed, or any equivalent specimens showing +the differences as to number of cotyledons and the presence or absence of +endosperm. Each student should be provided with several specimens, +both soaked and dry, of the kind under consideration. Corn, beans, and +wheat need to be soaked from 12 to 24 hours; squash and pumpkin from +2 to 5 days, and very hard seeds, like the castor bean and morning-glory, +from 5 to 10. If such seeds are <em>clipped</em>, before soaking, that is, if a small +piece of the coat is chipped away from the end opposite the scar, or eye, +they will soften more quickly. Keep them in a warm place with an even +temperature till just before they begin to sprout, when the contents become +softened. Very brittle cotyledons may be softened quickly by boiling +for a few minutes.</p> + +<p>No appliances are needed beyond the pupil’s individual outfit and some +of the food tests given in Section I of this chapter.</p> +</div> + + +<p id="p-11"><b>11. Dissection of a grain of corn.</b>—Examine a dry grain +of corn on both faces. What differences do you notice? +Sketch the grooved side, labeling the hard, yellowish outer<span class="pagenum" id="Page_13">[Pg 13]</span> +portion, <em>endosperm</em>, the depression near the center, <em>embryo</em>, or +<em>germ</em>.</p> + +<p>Next take a grain that has been soaked for twenty-four +hours. What changes do you see? How do you account for +the swelling of the embryo? Remove the skin and observe +its texture. Make an enlarged sketch of a grain on the +grooved side with the coat removed, labeling the flat oval body +embedded in the endosperm, <em>cotyledon</em>; the upper end of the +little budlike body embedded in the cotyledon, <em>plumule</em>, the +lower part, <em>hypocotyl</em>—words +meaning, respectively, “seed +leaf,” “little bud,” and +“the part under the cotyledon.” +As this part has not +yet differentiated into root +and stem, we cannot call it +by either of these names. +The cotyledon, hypocotyl, +and plumule together compose +the embryo. Pick out +the embryo and sketch as +it appears under the lens. +Crush it on a piece of white paper; what does it contain?</p> + +<figure class="figright illowp50" id="i_023" style="max-width: 31.25em;"> + <img class="w100" src="images/i_023.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 14-16.</span>—Dissection of a grain of +corn: 14, soaked grain, seen flatwise, cut +away a little and slightly enlarged, so as to +show the embryo lying in the endosperm; +15, in profile section, dividing the grain +through the embryo and cotyledon; 16, the +embryo taken out whole. The thick mass is +the cotyledon; the narrow body projecting +upwards, the plumule; the short projection +at the base, the hypocotyl (<i>after</i> <span class="smcap">Gray</span>).</p></figcaption> +</figure> + +<p>Make a vertical section of another soaked grain at right +angles to its broader face, and sketch, labeling the parts as +they appear in profile. Make a cross section through the +middle of another grain and sketch, labeling the parts as before. +What proportion of the grain is endosperm and what +embryo? Put a drop of iodine and of nitric acid separately +on pieces of the endosperm, and note the effects. Test the +seed coats and the cotyledon to see if they contain any starch.</p> + +<p>Notice that the corn grain has but one cotyledon, hence +such seeds are said to be <em>monocotyledonous</em>, or one-cotyledoned. +The grains are not typical seeds, but are selected for examination +because they are large and easy to handle, can be obtained +everywhere, and germinate readily.</p> + +<p><span class="pagenum" id="Page_14">[Pg 14]</span></p> + +<p id="p-12"><b>12. Dissection of a bean.</b>—Sketch a dry bean as it lies in +the pod, showing its point of attachment and any markings +that may appear on its surface. Then take it from the pod and +examine the narrow edge by which it was attached. Notice +the rather large scar (commonly called the eye of the bean) +where it broke away from the point of +attachment. This is the <em>hilum</em>. Near the +hilum, look for a minute round pore like +a pinhole. This is called the <em>micropyle</em>, +from a Greek word meaning “a little +gate,” because it is the entrance to the +interior of the seed coat. There was no +micropyle observed in the corn grain, +because it is not a true seed but a fruit +inclosing a single seed. The inclosing +membrane is the fruit skin, which has become incorporated +with the seed coat and taken its place as a protective covering. +Compare a soaked bean with a dry one; what difference do +you perceive? How do you account for the change in size and +hardness? Find the hilum and the micropyle in the soaked +bean. Lay it on one side and sketch, with the micropyle on +top; then turn toward you the narrow edge that +was attached to the pod and sketch, labeling all +the parts. Make a section through the long diameter +at right angles to the flat sides, press it +slightly open, and sketch it. Notice the line or +slit that seems to cut the section in half longitudinally, +and the small round object between the +halves at one end; can you tell what it is?</p> + +<figure class="figleft illowp30" id="i_024" style="max-width: 28.125em;"> + <img class="w100" src="images/i_024.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 17, 18.</span>—A kidney +bean: 17, side view; +18, front view, showing <i>h</i>, +hilum, <i>m</i>, micropyle.</p></figcaption> +</figure> + +<figure class="figright illowp20" id="i_024a" style="max-width: 25em;"> + <img class="w100" src="images/i_024a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 19 .</span>—Cotyledon of +a bean, showing +plumule.</p></figcaption> +</figure> + +<p>Slip off the coat from a whole bean and notice its +texture. Hold it up to the light and see if it shows +any signs of veining. See whether the scar at the hilum extends +through the kernel, or marks only the seed coat. Lay open the +two flat bodies into which the kernel divides when stripped of +its coats, keeping them side by side, with the part above the +micropyle toward the top. Sketch their inner face and label<span class="pagenum" id="Page_15">[Pg 15]</span> +them <em>cotyledons</em>. Be careful not to break or displace the tiny +bud packed away between the cotyledons, just above the +hilum. Label the round portion of this bud, <em>hypocotyl</em>, and +the upper, more expanded part, <em>plumule</em>. Which way does the +base of the hypocotyl point; toward the micropyle, or away +from it? Pick out this budlike body entire and sketch as it appears +under the lens. Open the plumule with a pin and examine +it with a lens; of what does it appear to consist? Do you +find any endosperm around the cotyledons, as in the corn and +oats? Break one of the soaked cotyledons, apply the proper +tests (Exps. 2, 3, 5), and report what substances it contains. +Where is the nourishment for the young plant stored? What +part of the bean gives it its value as food?</p> + +<p>Notice that in the bean the embryo consists of three parts, +the hypocotyl, plumule, and the two cotyledons, which completely +fill the seed coats, leaving no place for endosperm. +Seeds like the bean, squash, and castor bean, which have +two cotyledons, are said to be <em>dicotyledonous</em>.</p> + +<p id="p-13"><b>13. The castor bean.</b>—Lay a castor bean on a sheet +of paper before you with its flat side down; what does it +look like? The resemblance may be increased by soaking +the seed a few minutes, in order to swell the two little protuberances +at the small end. Can you think of any benefit +a plant might derive from this curious resemblance of its seed +to an insect?</p> + +<p>Sketch the seed as it lies before you, labeling the protuberance +at the apex, <em>caruncle</em>. The caruncle is an appendage +of the seed-covering developed by various plants; its use +is not always clear. What appears to be its object in the +castor bean? Refer to <a href="#exp-13">Exp. 13</a> and see if there is any other +purpose it might serve.</p> + +<p>Turn the seed over and sketch the other side. Notice the +colored line or stripe that runs from the large end to the caruncle. +This is the <em>rhaphe</em>, and shows the position that +would be occupied by the seed stalk if it were present. Its +starting point near the large end, which is marked in fresh<span class="pagenum" id="Page_16">[Pg 16]</span> +seeds by a slight roughness, is the <em>chalaza</em>, or organic base of +the seed, where the parts all come together like the parts of a +flower at their insertion on the stem. Where was it situated +in the common bean? How does this differ from its +position in the castor bean? Where the rhaphe ends, +just at the beak of the caruncle, you will find the hilum. +The micropyle is covered by the caruncle, which is an +outgrowth around it.</p> + +<figure class="figleft illowp50" id="i_026" style="max-width: 31.25em;"> + <img class="w100" src="images/i_026.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 20-22.</span>—Castor bean (slightly magnified); 20, +back view; 21, front view; <i>ch</i>, chalaza; <i>r</i>, rhaphe; <i>ca</i>, +caruncle; 22, vertical section; <i>en</i>, endosperm; <i>cc</i>, cotyledons; +<i>hy</i>, hypocotyl; <i>hi</i>, hilum; <i>m</i>, micropyle.</p></figcaption> +</figure> + +<p>Now cut a vertical section through a seed that has been +soaked for several days, at right angles to the broad sides, +and sketch it. Label the white, pasty mass within the +seed coats, endosperm. Can you make out what the narrow +white line running through the center of the endosperm, dividing +it into two halves, represents? Make a similar sketch +of a cross section. +Notice the same +white line running +horizontally across +the endosperm, dividing +it into two +equal parts. To +find out what these +lines are, take another +seed (always +use soaked seeds for +dissection) and remove the coats without injuring the kernel. +Split the kernel carefully round the edges, remove half the +endosperm, and sketch the other half with the delicate embryo +lying on its inner face. You will have no difficulty +now in recognizing the lines in your drawings as sections of +the thin cotyledons. Where is the hypocotyl, and which way +does its base point? Remove the embryo from the endosperm, +separate the cotyledons with a pin, hold them up to the light, +and observe their beautiful texture. Sketch them under the +lens, showing the delicate venation. Is there any plumule?</p> + +<p>Test the endosperm with a little iodine. Does it give a<span class="pagenum" id="Page_17">[Pg 17]</span> +blue or a brown reaction? Crush another bit of it on a piece +of white paper and see if it leaves a grease spot. What does +this show that it contains? Test the embryo in the same way, +and see whether it contains any oil.</p> + +<div class="blockquot"> + +<p><span class="smcap">Note.</span>—It should be borne in mind that the castor bean bears no relation +whatever to the true beans. It belongs to the spurge family, which +is botanically very remote from that of the peas and beans.</p> +</div> + +<figure class="figcenter illowp100" id="i_027" style="max-width: 50em;"> + <img class="w100" src="images/i_027.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 23-25.</span>—Seed of a squash; 23, seed from the outside; 24, vertical section +perpendicular to the broad side; 25, section parallel to the broad side, showing inner +side of a cotyledon; <i>a</i>, seed coat; <i>c</i>, cotyledons; <i>h</i>, hypocotyl; <i>p</i>, plumule.</p></figcaption> +</figure> + +<p id="p-14"><b>14. Study of a squash or gourd seed.</b>—How does the coat +of a squash seed differ from that of the bean? At the small +end, look for two dots, or pinholes, close +together. Refer to your drawing of the +bean and see if you can make out, with +the help of a lens, what they are. The +bean is a curved seed, which is bent so as +to bring the hilum close to the micropyle +on one side. But by far the greater +number of seeds are <em>inverted</em>, or turned +over on their stalks, as you sometimes +see huckleberry blossoms and bell flowers +on their stems, so that when the stalk +breaks away from its attachment, the +scar and the micropyle come close together +at one end, as in the squash seed.</p> + +<figure class="figright illowp30" id="i_027a" style="max-width: 18.75em;"> + <img class="w100" src="images/i_027a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 26.</span>—Diagram of +an inverted or anatropous +seed, showing the +parts in section: <i>a</i>, outer +coat; <i>b</i>, inner coat; <i>c</i>, +kernel; <i>d</i>, rhaphe; <i>ch</i>, +chalaza; <i>h</i>, hilum; <i>m</i>, +micropyle (<i>After</i> <span class="smcap">Gray</span>).</p></figcaption> +</figure> + +<p>Make a drawing of the outside of a +seed, labeling all the parts you have observed; then gently<span class="pagenum" id="Page_18">[Pg 18]</span> +remove the hard coat, or <em>testa</em>, as it is called. The thin, greenish +covering that lines it on the inside is the endosperm. How +does it compare in quantity with that in the corn and castor +bean? How do the cotyledons compare in thickness with +those of the bean? Carefully separate them and draw, labeling +the parts as you make them out. The tiny pointed +object between the cotyledons at their point of union is the +plumule; is it as well developed as in the bean? Can you see +any reason why seeds like the pea and bean, which have cotyledons +too thick and clumsy to do well the work of true leaves, +should have a well-developed plumule, while those with thin +cotyledons, like the squash and pumpkin, do not, as a general +thing, form a large plumule in the embryo? The little projection +in which the cotyledons end is the hypocotyl; which +way does it point? Where did you find the micropyle to be? +Test the cotyledons and some of the endosperm for food substances; +what do you find in them?</p> + +<p id="p-15"><b>15. Study of a pine seed.</b>—Remove one of the scales from +a pine cone and sketch the seed as it lies in place on the cone +scale. Notice its point of attachment to +the scale, and look near this point for a +small opening, which you can easily recognize +as the micropyle. The seed with its +wing looks very much like a fruit of the +maple, but differs from it in being a naked +seed borne on the inner side of a cone scale, +without a pod or husk or outer covering of +any kind, such as beans and nuts and grains +are provided with. Plants like the pine, +which bear their seed in this way, are called +<em>Gymnosperms</em>, a word that means “naked +seeds,” in contradistinction to the <em>Angiosperms</em>, which bear +their seeds in pods or other closed envelopes.</p> + +<table> +<tr> +<td class='tdc wd50'> +<figure class="figcenter illowp80" id="i_028" style="max-width: 15.5em;"> + <img class="w100" src="images/i_028.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 27, 28.</span>—Pitch +pine seeds: +27, scale, or open +carpel, with one seed +in place; 28, winged +seed, removed. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> +</td> +<td class='tdc wd50'> +<figure class="figcenter illowp80" id="i_029" style="max-width: 10.5em;"> + <img class="w100" src="images/i_029.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 29.</span>—Section +of pine seed, +showing the +polycotyledonous +embryo +(<span class="smcap">Gray</span>).</p></figcaption> +</figure> +</td></tr></table> + +<p class='cb'>Remove the coat from a seed that has been soaked for +twenty-four hours, and examine it with a lens. Does it consist +of one or more layers? Is there any difference in color<span class="pagenum" id="Page_19">[Pg 19]</span> +between the inner and outer layers? Look at the base of the +hypocotyl for some loose, cobwebby appendages. These are +the remains of other embryos with certain appendages +belonging to them that were formed in the +endosperm, but failed to develop. Did you find +remains of this kind in any of the other seeds examined? +Pick out the embryo from the endosperm +and test both for food substances. Which +of these do you find? Which are absent? How +does the embryo differ from those already examined? +How many cotyledons are there? Make +an enlarged sketch of a seed in longitudinal +section, labeling correctly all the parts observed.</p> + +<p id="p-16"><b>16. Comparison as to food value of seeds.</b>—Make in your +notebook a tabular statement after the model here given, of +the food contents found in the different seeds you have examined. +Indicate the relative quantity of each by writing +under it, in the appropriate column, the words, “much,” +“little,” or “none,” as the case may be.</p> + + +<p class="p2 center fs90 smcap">Model for Record of Seeds Examined</p> + +<table class="autotable fs80 wd80"> +<tr> +<td class="bt" colspan="5"></td> +</tr> +<tr> +<td class="tdc bt wd20 smcap" rowspan="2">Seeds Examined</td> +<td class="tdc bl bt" colspan="4"><span class='smcap'>Foods Tested</span></td> +</tr> +<tr> +<td class="tdc bl bt">Starch</td> +<td class="tdc bl bt">Sugar</td> +<td class="tdc bl bt">Oil</td> +<td class="tdc bl bt">Proteins</td> +</tr> +<tr> +<td class="tdl bt">Corn</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="tdl bt">Wheat</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="tdl bt">Bean</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="tdl bt">Squash</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="tdl bt">Castor bean</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="tdl bt">Pine</td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +<td class="bl bt"></td> +</tr> +<tr> +<td class="bt" colspan="5"></td> +</tr> +<tr> +<td class="bt" colspan="5"></td> +</tr> +</table> + +<p>By far the greater number of seeds contain endosperm; +that is, they consist of an embryo with more or less nourishing<span class="pagenum" id="Page_20">[Pg 20]</span> +matter stored about it. Even in seeds which appear to +have none, the endosperm is present at some period during +development, but is absorbed by the cotyledons before germination.</p> + +<p id="p-17"><b>17. Manner of storing nourishment.</b>—In the various seeds +examined, we have seen that the nourishment for the young +plant is either stored in the embryo itself, as in the cotyledons +of the bean, acorn, squash, etc., or packed about them +in the form of endosperm, as in the corn, wheat, and castor +bean.</p> + +<p id="p-18"><b>18. The number of cotyledons.</b>—Seeds are also classed +according to the number of their cotyledons, as having one, +two, or many cotyledons. The first two kinds make up the +great class of Angiosperms, which includes all the true flowering +plants and forms the most important part of the vegetation +of the globe. The last is characteristic of the great +natural division of Gymnosperms, or naked-seeded plants, +of which we have had an example in the pine. They are the +most primitive type of living seed-bearing plants. Though +they are not so abundant now as in past ages, numbering +only about four hundred known species, they present many +diversities of form, which seem to ally them on the one hand +with the lower, or spore-bearing plants (ferns, mosses, etc.), +and on the other hand with the Angiosperms.</p> + + +<div class="blockquot"> + +<h4>Practical Questions</h4> + +<p>1. Make a list of all the seeds you can find that have very thick cotyledons, +and underline those that are used as food by man or beast.</p> + +<p>2. Make a similar list of all the kinds with thin cotyledons and more or +less endosperm, that are used for food or other purposes.</p> + +<p>3. Do you find a greater number of foodstuffs among the one kind +than the other?</p> + +<p>4. How do the two kinds compare, as a general thing, in size and +weight?</p> + +<p>5. From what part of the castor bean do we get oil? of the peanut? +of cotton seed? (<a href="#exp-1">Exps. 1-6</a>.)</p> + +<p>6. Is there any valid objection to the wholesomeness of peanut oil, and +of cottonseed lard as compared with hog’s lard? (<a href="#p-1">1</a>, <a href="#p-3">3</a>.)</p> + +<p><span class="pagenum" id="Page_21">[Pg 21]</span></p> + +<p>7. What is bran? Does it contain any nourishment? (<a href="#p-11">11</a>, <a href="#p-12">12</a>; <a href="#exp-1">Exps. 1-6</a>.)</p> + +<p>8. What gives to Indian corn its value as food? to oats? wheat? +rice? (<a href="#p-3">3</a>; <a href="#exp-1">Exps. 1-6</a>.)</p> + +<p>9. Which of these grains has the larger proportion of endosperm to +embryo? (<a href="#i_012">Figs. 1-3</a>.)</p> + +<p>10. Which contains the larger amount of starch in proportion to +its bulk, rice or Indian corn?</p> + +<p>11. If you wished to produce a variety of corn rich in oil, you would +select seed for planting with what part well developed? (<a href="#p-3">3</a>; <a href="#i_012a">Figs. 4-7</a>.)</p> +</div> + + +<h3 id="CH_I_IV">IV. SEED DISPERSAL</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Fruits and seeds of any kind that show adaptations for +dispersal. Some common examples are: (1) Wind: ash, elm, maple, +ailanthus, milkweed, clematis, sycamore, linden, dandelion, thistle, +hawkweed. (2) Water: pecan, filbert, cranberry, lotus, hickory nut, +coconut—obtain one with the husk on, if possible. (3) Animal agency +(involuntary): cocklebur, tickseed, beggar-ticks, burdock; (voluntary) +almost all kinds of edible fruits, especially the bright-colored ones—wild +plums, cherries, haws, dogwood, persimmons, etc. (4) Explosive and +self-planting: witch-hazel, wood sorrel, violet, crane’s-bill, wild vetch, +peanut, medick, stork’s-bill (Erodium).</p> + +<p id="exp-17"><span class="smcap">Experiment 17. To show how seeds are dispersed by wind.</span>—Take +a number of winged and plumed fruits and seeds, such as those of the +maple, ash, ailanthus, dandelion, clematis, milkweed, and trumpet creeper; +stand on a chair or table in a place where there is a draft of air and let +them all go. Which travel the farther, the winged or the plumed kinds? +Which sort is better fitted to aërial transportation?</p> + +<p id="exp-18"><span class="smcap">Experiment 18. Dispersal by water.</span>—Place in a bucket of water +a hazelnut, an acorn, an orange, a cranberry, a pecan, a hickory nut, a fresh +apple, and a coconut with the husk on. Which are the best floaters? Cut +open or break open the good swimmers, compare with the non-floaters, and +see to what peculiarity of structure their floating qualities are due. In +what situations do the cranberry and the coconut grow? Can you see +any advantage to a plant so situated in producing fruits that float easily?</p> + +<p id="exp-19"><span class="smcap">Experiment 19. Dispersal by explosive capsules.</span>—Moisten +slightly some mature but unopened capsules of witch hazel, wood sorrel, +rabbit pea, or violet, and leave in a warm, dry place for fifteen to forty-five +minutes. What happens when the pods begin to dry? Measure the +distance to which the different kinds of seeds have been ejected. Which +were thrown farthest? What was the object of the movement? What +caused the explosion?</p> + +<p><span class="pagenum" id="Page_22">[Pg 22]</span></p> + +<p id="exp-20"><span class="smcap">Experiment 20. The use of adhesive fruits.</span>—Scatter broadcast +a handful of hooked or prickly seeds or fruits—cocklebur, tickseed, beggar-ticks, +bur grass, etc. Are they suited for wind transportation? Drop one +of them on your sleeve, or on the coat of a fellow student; will it stay +there? What would be the effect if it became attached to the fur of a +roaming animal? Is this a successful mode of dissemination?</p> +</div> + +<figure class="figcenter illowp100" id="i_032" style="max-width: 50em;"> + <img class="w100" src="images/i_032.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 30-32.</span>—30, A pod of wild vetch, with mature valves twisting spirally to +discharge the seed; 31, pod of crane’s-bill discharging its seed; 32, capsules of witch-hazel +exploding.</p></figcaption> +</figure> + +<figure class="figcenter illowp100" id="i_032a" style="max-width: 50em;"> + <img class="w100" src="images/i_032a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 33-36.</span>—Fruits adapted to wind dispersal: 33, winged pod of pennycress; +34, spikelet of broom sedge; 35, akene of Canada thistle; 36, head of rolling spinifex +grass.</p></figcaption> +</figure> + +<p id="p-19"><b>19. Agencies of dispersal.</b>—The means at nature’s disposal +for this purpose, as shown by the experiments just made, +are four; namely, wind, water, the explosion of capsules due +to the withdrawal of water, and the agency of animals, including +man. The first three are purely mechanical. The +last, animal agency, is either voluntary or involuntary, according +as it is conscious and intentional, or accidental merely. +Man, of course, is the only consciously voluntary agent. Of<span class="pagenum" id="Page_23">[Pg 23]</span> +the four agencies named, animals and wind are the most effective, +and the greater number of adaptations observed will be +found to have reference to these.</p> + +<table class='autotable'> +<tr><td class='vat'> +<figure class="figcenter illowp90" id="i_033xl" style="max-width: 23.0em;"> + <img class="w100" src="images/i_033xl.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 37.</span>—Good quality of clover seed.</p> + </figcaption> +</figure> +</td><td class='vat'> +<figure class="figcenter illowp90" id="i_033xr" style="max-width: 23.0em;"> + <img class="w100" src="images/i_033xr.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 38.</span>—Inferior quality of clover seed mixed with “screenings.”</p> + </figcaption> +</figure></td></tr></table> + +<figure class="figright illowp40" id="i_033b" style="max-width: 25em;"> + <img class="w100" src="images/i_033b.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 39.</span>—Dodder on red clover, +showing how the seeds get mixed.</p></figcaption> +</figure> + +<p id="p-20"><b>20. Involuntary dispersal.</b>—The lower animals may be +voluntary agents in a way, though not designedly so, as when +a squirrel buries nuts for his own use and then forgets the location +of his hoard and leaves them to germinate; or when +a jaybird flies off with a pecan in his bill, intending to crack +and eat it, but accidentally lets +it fall where it will sprout and +take root. Both man and the +lower animals are not only involuntary, +but often unwilling +agents of dispersal. Some of the +most troublesome weeds of civilization +have been unwittingly distributed +by man as he journeyed +from place to place, carrying, +along with the seed for planting +his crops, the various weed seeds, +or “screenings,” as these mixtures +are called by dealers, with which +they have been adulterated either through carelessness and +ignorance, or from unavoidable causes. The neglected +animals, also, that are allowed by short-sighted farmers to +wander about with their hair full of cockleburs and other<span class="pagenum" id="Page_24">[Pg 24]</span> +adhesive weed pests, are no doubt very unwilling carriers of +those disagreeable burdens.</p> + +<p id="p-21"><b>21. Tempting the appetite.</b>—This is the most important +adaptation to dispersal by animals. Have you ever asked +yourself how it could profit a plant to tempt birds and beasts +to devour its fruit, as so many of the bright berries we find in +the autumn woods seem to do? To answer this question, +examine the edible fruits of your neighborhood and you will +find that almost without exception the seeds are hard and +bony, and either too +small to be destroyed +by chewing, and thus +capable of passing +uninjured through +the digestive system +of an animal; or, if +too large to be swallowed +whole, compelling +the animal, +by their hardness or +disagreeable flavor, +to reject them. In +cases where the seeds +themselves are edible +and attractive, +the fruits are usually +armed during the +growing season with +protective coverings, +like the bur of the chestnut and the astringent hulls of the hickory +nut and walnut. The acidity or other disagreeable qualities +of most unripe fruits serves a similar purpose, while their +green color, by making them inconspicuous among the foliage +leaves, tends still further to insure them against molestation.</p> + +<figure class="figcenter illowp50" id="i_034" style="max-width: 25em;"> + <img class="w100" src="images/i_034.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 40-42.</span>—Adhesive fruits: 40, fruit of hound’s-tongue; +41, akene of bur marigold; 42, fruit of bur +grass (cenchrus).</p></figcaption> +</figure> + +<p id="p-22"><b>22. Voluntary agency.</b>—The cultivated fruits and grains +owe their distribution and survival almost entirely to the<span class="pagenum" id="Page_25">[Pg 25]</span> +voluntary agency of man. Dispersal by this means, whether +intentional or accidental, is purely artificial, and except in the +case of a few annuals like horseweed, bitterweed, ragweed, +goosefoot, and other field pests that have adjusted their season +of growth and flowering to the conditions of cultivation, +is not correlated with any special modification of the plants +for self-propagation. On the contrary, many of the most +widely distributed weeds of cultivation, such as the oxeye +daisy, the rib grass, mayweed and bitterweed, possess very +imperfect natural means of dispersal, and are largely dependent +for their propagation on the involuntary agency of man.</p> + +<p id="p-23"><b>23. Use of the fruit in dispersal.</b>—It will be seen from the +foregoing observations that the fruit plays a very important +part in the work +of dispersal, most +of the adaptations +for this purpose +being connected +with it. +In cases where a +number of seeds +are contained +in a large pod +that could not +conveniently be +blown about by +the breeze, +adaptations for +wind dispersal are attached to the individual seeds, as in the +willow, milkweed, trumpet creeper, and paulonia; but as a +general thing, adaptations of the seed are for protection, the +work of dispersal being provided for by the fruit. In the case +of the large class of plants known as “tumbleweeds,” the +whole plant body is fitted to assist in the work of transportation. +Such plants generally grow in light soils and either +have very light root systems, or are easily broken from their<span class="pagenum" id="Page_26">[Pg 26]</span> +anchorage and left to drift about on the ground. The spreading, +bushy tops become very light after fruiting, so as to be +easily blown about by the wind, dropping their seeds as they +go, until they finally get stranded in ditches and fence corners, +where they often accumulate in great numbers during the +autumn and winter.</p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp80" id="i_035_43" style="max-width: 38.25em;"> + <img class="w100" src="images/i_035_43.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig.</span> 43.—A fruiting plant of winged pigweed (<i>Cycloloma</i>), showing the bunchy top and weak anchorage of a typical tumbleweed.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp80" id="i_035_44" style="max-width: 31.125em;"> + <img class="w100" src="images/i_035_44.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig.</span> 44.—Panicle of “old witch grass,” a common tumbleweed.</p> + </figcaption> +</figure></td></tr></table> + +<p id="p-24"><b>24. The advantages of dispersal.</b>—Seed cannot germinate +unless they are placed in a suitable location as to soil, moisture, +and temperature. In order to increase the chances of securing +these conditions, it is clearly to the advantage of a species +that its seeds should be dispersed as widely as possible, both +that the seedlings may have plenty of room, and that they +may not have to draw their nourishment from soil already +exhausted by their parents. The farmer recognizes this +principle in the rotation of +crops, because he knows that +successive growths of the +same plant will soon exhaust +the soil of the substances required +for its nutrition, while +they may leave it richer in +nourishment for a different +crop.</p> + +<figure class="figcenter illowp40" id="i_036" style="max-width: 25em;"> + <img class="w100" src="images/i_036.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 45.</span>—Self-planting pod of peanut.</p></figcaption> +</figure> + +<p id="p-25"><b>25. Self-planting seeds.</b>—Dispersal +is not the only +problem the seed has to meet. +The majority of seeds cannot +germinate well on top of the +ground, and must depend on +various agencies for getting +under the soil. Some of them +do this for themselves. The +seeds of the stork’s-bill, popularly known as “filarees,” have +a sharp-pointed base and an auger-shaped appendage at the +apex, ending in a projecting arm (the “clock” of the filaree) +by which it is blown about by the wind with a whirling motion<span class="pagenum" id="Page_27">[Pg 27]</span> +till it strikes a soft spot, when it begins at once to bore its +way into the ground. The common peanut is another example. +The blossoms are borne under the leaves, near the base +of the stem, and as soon as the seeds begin to form, the +flower stalks lengthen several inches, carrying the young pods +down to the ground, where they bore into the soil and ripen +their seeds.</p> + + +<div class="blockquot"> + +<h4>Practical Questions</h4> + +<p>1. Name the ten most troublesome weeds of your neighborhood.</p> + +<p>2. What natural means of dispersal have they?</p> + +<p>3. Which of them owe their propagation to man?</p> + +<p>4. Are there any tumbleweeds in your neighborhood?</p> + +<p>5. Would you expect to find such weeds in a hilly or a well-wooded +region? (<a href="#p-19">19</a>, <a href="#p-23">23</a>; <a href="#exp-17">Exp. 17</a>.)</p> + +<p>6. What situations are best fitted for their propagation? (<a href="#p-19">19</a>, <a href="#p-23">23</a>; +<a href="#exp-17">Exp. 17</a>.)</p> + +<p>7. Make a list of all the fruits and seeds you can think of that are +adapted to dispersal by wind; by water; by animals.</p> + +<p>8. By what means of dissemination, or protection, or both, is each of +the following distinguished: the squash; apple; fig; pecan; poppy; +bean; beggar-tick; linden; grape; rice; pepper; olive; cranberry; +jimson weed; thistle; corn; wheat; oats?</p> + +<p>9. What is the agent of dispersion, or what the danger to be provided +against, in each case?</p> + +<p>10. Could our cultivated fruits and grains survive in their present state +without the agency of man? (<a href="#p-22">22</a>.)</p> + +<p>11. Name all the plants you can think of that bear winged seeds and +fruits; are they, as a general thing, tall trees and shrubs, or low herbs?</p> + +<p>12. Name all you can think of that bear adhesive seeds and fruits; are +they tall trees or low herbs?</p> + +<p>13. Give a reason for the difference. (<a href="#exp-17">Exps. 17</a>, <a href="#exp-20">20</a>.)</p> + +<p>14. Why is the dandelion one of the most widely distributed weeds in +the world? (<a href="#p-19">19</a>; <a href="#exp-17">Exp. 17</a>.)</p> + +<p>15. Is the wool that covers cotton seed for dispersal or protection?</p> + +<p>16. What advantage to the Indian shot (canna) is the excessive hardness +of its seeds? (<a href="#p-21">21</a>.)</p> + +<p>17. What is the use to the species, of the bitter taste of lemon and +orange seed? (<a href="#p-21">21</a>.)</p> + +<p>18. Why are the seeds of dates and persimmons and haws so hard? +(<a href="#p-21">21</a>.)</p> + +<p><span class="pagenum" id="Page_28">[Pg 28]</span></p> + +<p>19. Do you find any edible seeds without protection? If so, account +for the want of it. (<a href="#p-21">21</a>, <a href="#p-22">22</a>.)</p> + +<p>20. Name some of the agencies that may assist in covering seeds with +earth.</p> + +<p>21. Do you know of any seeds that bury themselves?</p> + +<p>22. The seeds of weeds and other refuse found mixed with grain sold +on the market are known, commercially, as “screenings.” Wheat brought +to mills in Detroit showed screenings that contained, among other things, +seeds of black bindweed, green foxtail grass, yellow foxtail, chess, oats, +ragweed, wild mustard, corn cockle, and pigweed. Can you mention some +of the ways in which these foreign substances may have gotten into the +crop and suggest means for keeping them out?</p> + + +<h4 id="CH_I_FIELD">Field Work</h4> + +<p>The subjects treated in the foregoing chapter are, in general, better +suited to laboratory than to field work. There are some details, however, +which can be observed to advantage out of doors. Many of the seeds +found in your walks will show peculiarities of shape and external markings +and color that will invite observation. Examine also the contents of different +kinds you may meet with, as to the presence or absence of endosperm +and the arrangement and development of the embryo. Note: (1) whether, +as a general thing, there is any difference in size and weight and amount of +nourishing matter in the two kinds; (2) the greater variety in the shape +and arrangement of the cotyledons in the albuminous kind, and in the arrangement +of the embryo; (3) the differences in the development of +the plumule in the two kinds,—and give a reason for the facts observed.</p> + +<p>Among the different seeds you may find, look for adaptations for dispersal, +and decide to what particular method each is suited. Study the agencies +by which various kinds may get covered with soil. If the common stork’s-bill +(<i>Erodium cicutarium</i>) grows in your neighborhood, its seeds will well +repay a little study, and if there is a field of peanuts within reach, do not +fail to pay it a visit.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_29">[Pg 29]</span></p> + +<h2 class="nobreak" id="CH_II">CHAPTER II. GERMINATION AND GROWTH</h2> +</div> + + +<h3 id="CH_II_I">I. PROCESSES ACCOMPANYING GERMINATION</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A pint or two of corn, peas, beans, or any quickly germinating +seed.</p> + +<p><span class="smcap">Appliances.</span>—Matches; wood splinters; gas jet or alcohol lamp; +test tubes; a small quantity of mercuric oxide; a thermometer; a couple +of two-quart preserve jars, and a smaller wide-mouthed bottle that can +be put into one of them; some limewater; a glass tube (the straws used +by druggists for soft drinks will answer).</p> +</div> + +<p id="p-26"><b>26. Preliminary exercises.</b>—Before taking up the study +of germinating seeds, it is important to learn from what +sources the organic substances used by the growing plant +are derived, and some of the processes that accompany +growth and development.</p> + +<div class="blockquot"> + +<p id="exp-21"><span class="smcap">Experiment 21. To show the changes that accompany oxidation.</span>—Strike +a match and let it burn out. Examine the burnt portion +remaining in your hand; what changes do you notice? These changes +have been caused by the union of some substance in the match with +something outside of it, in the act of burning; let us see if we can find +out what this outside substance is.</p> + +<p id="exp-22"><span class="smcap">Experiment 22. To show the active agent in oxidation.</span>—Heat +some mercuric oxide in a test tube over the flame of a burner. +The heat will cause the oxygen to separate from the mercury, and in a +short time the tube will be filled with the gas. Extinguish the flame +from a lighted splinter and thrust the glowing end into the tube; what +happens? The oxygen unites with something in the wood and causes it to +burn just as the match did. Compare your burnt splinter with the burnt +end of the match; what resemblance do you notice between them?</p> + +<p id="exp-23"><span class="smcap">Experiment 23. To show that carbon dioxide is a product of +oxidation.</span>—Your experiment with the match showed that ignition +is accompanied by heat, and if active enough, by light, and also that +it left behind a solid substance in the form of charcoal. But how +about the part that united with the oxygen to produce these results?<span class="pagenum" id="Page_30">[Pg 30]</span> +Let us see what became of it. Hold a lighted candle under the open end +of a test tube, or under the mouth of a small glass jar. Does any vapor +collect on the inside? After two or three minutes quickly invert the jar +or the tube, and thrust in a lighted match: what happens? Can the +substance now in the jar be ordinary air? Why not? (Exps. 21, 22.) +Pour in a small quantity of limewater, holding your hand over the mouth +of the tube to prevent the air from getting in; the gas inside, being heavier +than air, will not escape immediately unless agitated. What change do +you notice in the limewater?</p> + +<p>It has been proved by experiment that the kind of gas formed by the +burning candle has the property of turning limewater milky; hence, +whenever you see this effect produced in limewater, you may conclude +that this gas, known as <em>carbon dioxide</em>, is present; and conversely, the +presence of carbon dioxide, especially if accompanied by some of the other +effects observed, as the giving out of heat and moisture, may be taken as +evidence that some process similar to that going on in the burning candle +is, or has been, at work.</p> + +<p id="exp-24"><span class="smcap">Experiment 24. Do these effects accompany any of the life +processes of animals?</span>—Blow your breath against the palm of your +hand; what sensation do you feel? Blow it against a mirror, or a piece +of common glass; what do you see? Blow through a +tube into the bottom of a glass containing limewater; +how is the water affected? How do these facts correspond +with the results of <a href="#exp-23">Exp. 23</a>?</p> + +<p id="exp-25"><span class="smcap">Experiment 25. Is there any evidence that +a similar process goes on in plants?</span>—(1) Half fill +a small, wide-mouthed jar with limewater, place it inside +a larger one (<a href="#i_040">Fig. 46</a>), and fill the space between +them, up to the neck of the smaller vessel, with well-soaked +peas, beans, or barleycorns, on a bed of moist +cotton or blotting paper. Cover with a piece of glass +and keep at a moderately warm temperature. (2) As +a control experiment, place beside this another jar arranged +in precisely the same way, except that seeds +must be used whose vitality has been destroyed by +heat. To prevent the entrance of germs among the +dead seeds, which might cause fermentation and thus +interfere with the experiment, set the jar containing them in a vessel of +water and boil an hour or two before the experiment begins. Otherwise, +treat precisely as in (1).</p> + +<figure class="figleft illowp20" id="i_040" style="max-width: 18.75em;"> + <img class="w100" src="images/i_040.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 46.</span>—Diagrammatic +section, +showing arrangement +of jars for +Exp. 25.</p></figcaption> +</figure> + +<p>After germination has taken place in (1), what change do you notice in +the limewater? If the effect is not apparent, gently stir with a straw or +<span class="pagenum" id="Page_31">[Pg 31]</span> +a glass rod to mix it with the gas in the larger jar. Has the limewater in +the control experiment undergone the same change? (It may show a +slight milkiness due to the carbon dioxide in the air.) Insert a thermometer +among the seeds in both of the larger jars, and compare their temperature +with that of the outside air; which shows the greater rise? +From this experiment and the last one, what process, common to animals, +would you conclude has been going on in the germinating seeds?</p> + +<p><span class="smcap">Note.</span>—Heat in germinating seeds is not always due to this cause +alone, but is sometimes increased by the presence of minute organisms +called bacteria. Germinating barley and rye in breweries sometimes +show an increase in temperature of 40 to 70 degrees, due to these organisms, +and spontaneous combustion in seed cotton has been reported from the +same cause.</p> +</div> + +<p id="p-27"><b>27. Oxidation.</b>—The process that brought about the +results observed in the foregoing experiments, and popularly +known as <em>combustion</em>, is more accurately defined by chemists +as <em>oxidation.</em> It takes place whenever substances enter into +new combinations with oxygen. The most familiar examples +of it are when oxygen enters into combination with substances +containing carbon. It was the union of a portion of the +oxygen of the air in <a href="#exp-21">Exp. 21</a>, and of that in the tube in <a href="#exp-22">Exp. +22</a>, with some of the carbon in the wood, that caused the +burning. The effect was more marked in the second case +because the oxygen in the tube was pure, while in the air it +is mixed with other substances.</p> + +<p id="p-28"><b>28. Carbon.</b>—The black substance left in your hand +after oxidation of the wood in Exps. 21 and 22 is <em>carbon</em>. +It composes the greater part of most plant bodies, and, in +fact, is the most important element in the realm of organic +nature. There is not a living thing known, from the smallest +microscopic germ to the most gigantic tree in existence, that +does not contain carbon as one of its essential constituents.</p> + +<p id="p-29"><b>29. Carbon dioxide.</b>—The gas produced by the burning +candle in <a href="#exp-23">Exp. 23</a>, by the germinating seeds in <a href="#exp-25">Exp. 25</a>, and +expelled from your own lungs in <a href="#exp-24">Exp. 24</a>, is carbon dioxide. +Chemists designate it by the symbol CO<sub>2</sub>, which means that +it consists of one part carbon to two parts oxygen. It is an<span class="pagenum" id="Page_32">[Pg 32]</span> +invariable product wherever the oxidation of substances +containing carbon goes on. Heat and moisture are evolved +at the same time, and if oxidation is very active, as in <a href="#exp-21">Exps. +21</a> and <a href="#exp-22">22</a>, light also. When the process takes place very +slowly, no light is evolved, and so little heat as to be imperceptible +without special observation. Hence, oxidation may +go on around us and even in our own bodies without our +being conscious of the fact.</p> + +<p>Carbon dioxide is of prime importance to the well-being of +plants. It furnishes the material from which the greater +part of their organic food is derived, as will be seen when +we take up the study of the leaf and its work. To animals, +on the contrary, its presence is so injurious that if the proportion +of it in the air we breathe ever rises much above 1 +part to 1000, the ill effects become painfully sensible. It +is not, however, as was formerly supposed, a poison, the +harm it does being to decrease the proportion of oxygen +in the atmosphere so that animals cannot get enough of it +to breathe, and die of suffocation.</p> + +<p id="p-30"><b>30. Respiration in plants and in animals.</b>—It was shown +in <a href="#exp-24">Exp. 24</a> that respiration in animals is accompanied by the +products of oxidation; hence we conclude that respiration +is a form of oxidation. And since these same products are +given off by plants (<a href="#exp-25">Exp. 25</a>), the inference is clear that the +same process goes on in them. But in plants the life functions +are so much more sluggish than in animals that it is +only in their most active state, during germination and +flowering, that evidence of it is to be looked for.</p> + +<p id="p-31"><b>31. Respiration and energy.</b>—In plants, as in animals, +respiration is the expression or measure of energy. Sleeping +animals breathe more slowly than waking ones, snakes and +tortoises more slowly than hares and hawks. The more +we exert ourselves and the more vital force we expend, the +harder we breathe; hence, respiration is more active in +children than in older persons and in working people than in +those at rest. It is the same with plants; respiration is most<span class="pagenum" id="Page_33">[Pg 33]</span> +perceptible in germinating seeds and young leaves, in buds +and flowers, where active work is going on. Hence, in this +condition they consume proportionately larger quantities +of oxygen and liberate correspondingly larger quantities of +carbon dioxide, with a proportionate increase of heat. In +some of the arums,—calla lily, Jack-in-the-pulpit, colocasia, +etc.,—and in large heads of compositæ, like the sunflower, +where a great number of small flowers are brought +together within the same protecting envelope, the rise of +temperature is sometimes so marked that it may be perceived +by placing a flower cluster against the cheek.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. What is charcoal? (<a href="#p-28">28</a>.)</p> + +<p>2. Is any of this substance contained in the seed? in the flour and +meal made from seed? (<a href="#p-28">28</a>; <a href="#exp-25">Exp. 25</a>.)</p> + +<p>3. What combination takes place when the cook lets the stove get too +hot and burns the biscuits? (<a href="#p-27">27</a>, <a href="#p-28">28</a>.)</p> + +<p>4. Of what does the burned part consist? (<a href="#p-28">28</a>.) What was it before +it was burned? (<a href="#p-27">27</a>, <a href="#p-28">28</a>).</p> + +<p>5. Which burns the more readily, an oily seed or a starchy one? +Which leaves the more solid matter behind? (Suggestion: test by putting +a bean, or a large grain of corn, and an equal quantity of the kernel +of a Brazil nut on the end of a piece of wire and thrusting into a flame.)</p> + +<p>6. Is there any rational ground for the statement that the wooden +buildings formerly used on Southern plantations as cotton ginneries were +sometimes destroyed through spontaneous combustion due to the heat +generated by piles of decaying cotton seed? (<a href="#exp-25">Exp. 25</a>, Note.)</p> +</div> + + +<h3 id="CH_II_II">II. CONDITIONS OF GERMINATION</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Several ounces each of various kinds of seed. For the +softer kinds, pea, bean, corn, oats, wheat are recommended; for those +with harder coverings, squash, castor bean, apple, pear, or, where obtainable, +cotton; for still harder kinds, persimmon and date seeds, or the +stones of plum and cherry.</p> + +<p><span class="smcap">Appliances.</span>—1 dozen common earthenware plates for germinators; +1 dozen two-ounce wide-mouthed bottles; 2 common glass tumblers; +clean sand, sawdust, or cotton batting, for bedding; a double boiler; a +gas burner, or a lamp stove.</p> +</div> + +<p><span class="pagenum" id="Page_34">[Pg 34]</span></p> + +<p id="p-32"><b>32. Recording observations.</b>—For this purpose a page +should be ruled off in the notebook of each student, after +the model here given, and the facts brought out by the different +experiments set down as observed.</p> + + +<p class="p2 center fs80 smcap">Number of Seeds Germinated</p> + +<table class="autotable fs80 wd80"> +<tr> +<td class="bt" colspan="12"></td> +</tr> +<tr> +<td class="tdl bt">No. of hours</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt">24</td> +<td class="tdc bl bt">48</td> +<td class="tdc bl bt">72</td> +<td class="tdc bl bt">4 d.</td> +<td class="tdc bl bt">5 d.</td> +<td class="tdc bl bt">6 d.</td> +<td class="tdc bl bt">7 d.</td> +<td class="tdc bl bt">8 d.</td> +<td class="tdc bl bt">10 d.</td> +<td class="tdc bl bt">2 w.</td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">1</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">2</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">3</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">4</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">5</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="tdl">No. of vessel</td> +<td class="tdc bl bt">6</td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +<td class="tdc bl bt"></td> +</tr> +<tr> +<td class="bt" colspan="12"></td> +</tr> +<tr> +<td class="bt" colspan="12"></td> +</tr> +</table> + +<div class="blockquot"> + +<p id="exp-26"><span class="smcap">Experiment 26. Can seeds have too much moisture?</span>—Drop a +number of dry beans or grains of corn, oats, or other convenient seed, +into a vessel with a bedding of cotton or paper that is barely moistened, +and an equal number of soaked seeds of the same kind into another vessel +with a saturated bedding of the same material. In a third vessel place +the same number of soaked seed, covering them partially with water, and +in a fourth cover the same number entirely. Label them 1, 2, 3, and 4; +keep all together in a warm, even temperature, and observe at intervals +of twenty-four hours for a week. What condition as to moisture do +you find most favorable to germination? Would seeds germinate in the +entire absence of moisture? How do you know?</p> + +<p id="exp-27"><span class="smcap">Experiment 27. Was it the presence of too much water, or +the lack of air caused by it, that interfered with germination +in the last experiment?</span>—To answer this question experimentally is +not easy, since it is difficult to obtain a complete vacuum without special +appliances. The simplest way is to fill with mercury a glass tube 30 +inches long, closed at one end, and invert it over a small vessel—a teacup, +or an egg cup will answer—containing mercury enough to cover +the bottom to a depth of two or three centimeters (see Appendix, Weights +and Measures, for English equivalents.) The tube must be supported in +such a way that its lower end will dip into the mercury without touching +the bottom of the vessel. With a pair of forceps insert under the mouth of +the tube two or three seeds that have been well soaked in water deprived +of air by previous boiling. Being lighter than mercury, they will float to +the top, where there is a complete absence of air while other conditions<span class="pagenum" id="Page_35">[Pg 35]</span> +favorable to germination are present. Before releasing, they should be +well shaken under the mercury to free them from air bubbles, and if the +coats are loose fitting so that they can be removed without injury to the +parts inclosed in them, they should be slipped off in order to get rid of any +imprisoned air they may contain. Additional moisture may be supplied, +if necessary, by injecting, by means of a medicine dropper inserted under +the mouth of the tube, a drop or two of water that has been previously +boiled. Keep in a warm, even temperature, under conditions favorable +to germination, and compare the behavior of the seeds with those placed +in the different vessels in <a href="#exp-26">Exp. 26</a>.</p> + +<p>If appliances for this experiment are lacking, a rough approximation +can be made by using the seeds of aquatic plants, such as the lotus, water +lily, and the so-called Chinese sacred bean, sold in the variety stores, +which we know are capable of germinating in the limited amount of air +contained in ordinary soil water. Place an equal number of such seeds, +of about the same size and weight, on a bedding of common garden soil +in two glass tumblers. Fill one vessel a little over half full of ordinary +soil water and the other to the same height with +water from which the air has been expelled by boiling. +Pour over the liquid a film of sweet oil or castor +oil, to prevent the access of air, leaving the surface of +the water in the other vessel exposed. In which do +the seeds come up most freely?</p> + +<figure class="figright illowp20" id="i_045" style="max-width: 12.5em;"> + <img class="w100" src="images/i_045.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 47.</span>—To find +out the proper depth +at which to plant +seeds.</p></figcaption> +</figure> + +<p>Some seeds, especially those rich in proteins, as +peas and beans, will germinate in a vacuum, because +oxygen is supplied for a time by the chemical decomposition +of substances in their tissues which contain it, +but when these are exhausted, respiration ceases and +death ensues.</p> + +<p id="exp-28"><span class="smcap">Experiment 28. Does the depth at which seeds +are planted affect their germination?</span>—Plant a +number of peas or grains of corn at different depths +in a wide-mouthed glass jar filled with moist sand, as +shown in <a href="#i_045">Fig. 47</a>, the lowest ones at the bottom, the +top ones barely covered. Try different kinds of seed +and grain,—radish, squash, cotton, or wheat,—and +watch them make their way to the surface. Do you +notice any difference in this respect between large +seed and small ones? Between those with thick cotyledons +and thin ones? At what depth do you find, +from your recorded observations, that seed germinate +best?</p> + +<p><span class="pagenum" id="Page_36">[Pg 36]</span></p> + +<p id="exp-29"><span class="smcap">Experiment 29. What temperature is most favorable to germination?</span>—Put +half a dozen soaked beans on moist cotton or sawdust in +three wide-mouthed bottles of the same size or in germinators arranged as +in <a href="#i_046x">Figs. 48, 49</a>, the seed also being selected +with a view to similarity of size and weight. +Keep one at a freezing temperature; the +second in a temperature of 15° to 20° C. +(see Appendix for Fahrenheit equivalents); +and the third, at 30° C. If a place can +be found near a stove or a register, where +an even temperature of about 125° F. +is maintained, place a fourth receptacle +there. Observe at intervals of twenty-four +hours for a week or ten days, keeping +the temperature as even as possible, and +maintaining an equal quantity of moisture +in each vessel. Make a daily record of +your observations. What temperature do +you find most favorable to germination?</p> + +<figure class="figcenter illowp30" id="i_046x" style="max-width: 25em;"> + <img class="w100" src="images/i_046x.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 48, 49.</span>—Home-made germinators: +48, closed; 49, showing interior arrangement.</p></figcaption> +</figure> + +<p id="exp-30"><span class="smcap">Experiment 30. At what temperature do seeds lose their vitality?</span>—Place +about two dozen each of grains of corn, beans, squash +seed, and castor beans, with an equal number of plum or cherry stones, +in water, and heat to a temperature of 150° F. After an exposure of +ten minutes, take out six of each kind and place in germinators made +of two plates with moist sand or damp cloth between them, as shown +in <a href="#i_046x">Figs. 48, 49</a>. Raise the temperature to 175° F., and after ten minutes +take out six more of each kind of seed and place in another germinator. +Raise the water in the vessel to 200°, take out another batch of seeds; +raise to the boiling point for ten minutes more, and plant the remaining +six of each lot. Number the four germinators, and observe at intervals +of twenty-four hours for two weeks. The harder kinds should be +kept under observation for three or four weeks, as they germinate slowly.</p> + +<p>Try the same experiments with the same kinds of seeds at a dry heat, +using a double boiler to prevent scorching, and record observations as before.</p> + +<p id="exp-31"><span class="smcap">Experiment 31. Time required for germination.</span>—Arrange in +germinators seeds of various kinds, such as corn, wheat, peas, turnip, apple, +orange, grape, castor bean, etc. “Clip” some of the harder ones and keep +all the kinds experimented with under similar conditions as to moisture, +temperature, etc., and record the time required for each to sprout. What +is the effect of clipping, and why?</p> + +<p id="exp-32"><span class="smcap">Experiment 32. Are very young or immature seeds capable of +germinating?</span>—Plant some seeds from half-grown tomatoes, and grains<span class="pagenum" id="Page_37">[Pg 37]</span> +of wheat, oats, or barley before they are ready for harvesting. Try as +many kinds as you like, and see how many will come up. Notice whether +there is any difference in the health and vigor of plants raised from seeds +in different stages of maturity.</p> + +<p id="exp-33"><span class="smcap">Experiment 33. The relative value of perfect and inferior +seed.</span>—From a number of seeds of the same species select half a dozen of +the largest, heaviest, +and most perfect, and +an equal number of +small, inferior ones. If +a pair of scales is at +hand, the different sets +should be weighed and +a record kept for comparison +with the seedlings +at the end of the +experiment. Plant the +two sets in pots containing +exactly the +same kind of soil, and +keep under identical +conditions as to light, +temperature, and +moisture. Keep the +seedlings under observation +for two or three +weeks, making daily +notes and occasional +drawings of the height +and size of the stems, +and the number of +leaves produced by +each.</p> +</div> + +<figure class="figright illowp60" id="i_047" style="max-width: 25em;"> + <img class="w100" src="images/i_047.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 50, 51.</span>—Stem development of seedlings: 50, +raised from healthy grains of barley; weight, 39.5 +grams (about 500 grs.); 51, raised under exactly similar +conditions from the same number of inferior grains; +weight, 23 grams (about 350 grs.).</p></figcaption> +</figure> + +<figure class="figright illowp60" id="i_047x" style="max-width: 25em;"> + <img class="w100" src="images/i_047x.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 52, 53.</span>—Improvement of corn by selection: +52, original type; 53, improved type developed from it.</p></figcaption> +</figure> + +<p id="p-33"><b>33. Resistance +to heat and cold.</b>—In +making experiments +with regard to temperature, notice how the extremes +tolerated are influenced, first, by the length of time the +seeds are exposed; second, by the amount of water contained +in them; and third, by the nature of the seed coats. Every +farmer knows that the effect of freezing is much more injurious<span class="pagenum" id="Page_38">[Pg 38]</span> +to plants or parts of plants when full of sap (water) +than when dry. This, in the opinion of the most recent +investigators, is because the water in the spaces outside the +cells freezes first and as moisture is gradually withdrawn +from the inside to take its place, the soluble salts which may +be present in the cell sap become more concentrated, and by +their chemical action on the contained proteins cause them +to be precipitated, or “salted out,” as we see sugar or salt +precipitated from solutions of those substances when water +is withdrawn by evaporation. In this way, it is believed, +the fundamental protoplasm of the cell may be so disorganized +that death ensues if the freezing is continued long enough, +since the protein precipitates become “denatured” and cannot +be reabsorbed if kept in a solid state too long. The length of +time necessary to produce death from this cause is, of course, +different in different plants, according to the kind of salts +dissolved in the sap and the nature of the proteins acted on +by them. The proteins in the sap of Begonia, or Pelargonium, +plants which are very sensitive to cold, yield a denatured +precipitate at, or a little below the freezing point of +water, while those of winter rye withstand a temperature of +-15° C., and of pine needles, -40° C.</p> + +<p>Mechanical injury through rupture of parts by freezing +is not apt to cause serious damage except in cases of sudden +and violent cold at a time when the tissues are gorged with +sap, as not infrequently happens during the abrupt changes +of temperature which sometimes occur in spring after the +trees have put forth their leaves. In an extreme case of +this kind, the writer has seen the trunk of an oak a foot +or more in diameter split in deep seams from the effects +of freezing.</p> + +<p id="p-34"><b>34. The length of time during which seeds may retain +their vitality.</b>—No direct experiment can be made to test +this point, since it would require months, or even years, +covering in some instances more than the lifetime of a generation. +It has been stated on good authority that seeds of the<span class="pagenum" id="Page_39">[Pg 39]</span> +water chinquapin (Nelumbo) have germinated after more +than a hundred years, and moss spores preserved in herbariums, +after fifty. But the records in such cases are not +always trustworthy, and there is absolutely no foundation +for the statements sometimes made about the germination +of wheat grains found preserved with mummies over two +thousand years old. If kept perfectly dry, however, seed +may sometimes be preserved for months, or even years. +Peas have been known to sprout after ten years, red clover +after twelve, and tobacco after twenty. Ordinarily, however, +the vitality of seeds diminishes with age, and in making experiments +it is best to select fresh ones. Those used for +comparison should also, as far as possible, be of the same size +and weight.</p> + +<p id="p-35"><b>35. Effect of precocious germination.</b>—It has been found +by experiment that plants raised from immature seed, when +they will germinate at all (<a href="#exp-32">Exp. 32</a>), yield earlier and larger +crops than the same kinds from mature seed. Early tomatoes +and some other vegetables are produced in this way. +The majority of seeds, however, require a period of rest +before beginning their life work. Those that are forced to +take up the burden of “child labor” show the effect of +such abnormal condition by yielding fruits that are smaller +and less firm than those raised from mature seed, so that +they do not keep well and have to be marketed quickly. +Under what circumstances does it pay to cultivate such +fruits?</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. What are the principal external conditions that affect germination? +(<a href="#exp-26">Exps. 26-29</a>.)</p> + +<p>2. What effect has cold? want of air? too much water?</p> + +<p>3. Is light necessary to germination?</p> + +<p>4. What is the use of clipping seeds? (<a href="#exp-12">Exps. 12</a>, <a href="#exp-13">13</a>, <a href="#exp-14">14</a>, and Material, +<a href="#Page_12">p. 12</a>.)</p> + +<p>5. In what cases should it be resorted to? (<a href="#exp-31">Exp. 31</a>.)</p> + +<p>6. Why will seed not germinate in hard, sunbaked land without<span class="pagenum" id="Page_40">[Pg 40]</span> +abundant tillage? Why not on undrained or badly drained land? (<a href="#exp-26">Exps. +26</a>, <a href="#exp-27">27</a>.)</p> + +<p>7. Will seeds that have lost their vitality swell when soaked? (<a href="#exp-16">Exp. 16</a>.)</p> + +<p>8. Are there any grounds for the statement that the seeds of plums +boiled into jam have sometimes been known to germinate?<a id="FNanchor_1" href="#Footnote_1" class="fnanchor">[1]</a> (<a href="#p-33">33</a>; <a href="#exp-30">Exp. 30</a>.)</p> + +<p>9. Could such a thing happen in the case of apple or sunflower seed, +and why or why not? (<a href="#p-33">33</a>.)</p> + +<p>10. Does it make any difference in the health and vigor of a plant +whether it is grown from a large and well-developed seed or from a weak +and puny one? (<a href="#exp-33">Exp. 33</a>.)</p> + +<p>11. Would a farmer be wise who should market all his best grain and +keep only the inferior for seed?</p> + +<p>12. What would be the result of repeated plantings from the worst +seed?</p> + +<p>13. Of constantly replanting the best and most vigorous?</p> + +<p>14. Suppose seed would germinate without moisture; would this be +an advantage, or a disadvantage to agriculturists?</p> + +<p>15. Why is a cool, dry place best for keeping seeds? (<a href="#exp-26">Exps. 26</a>, <a href="#exp-29">29</a>.)</p> + +<p>16. Why are the earliest tomatoes found in the market usually smaller +than those offered later? (<a href="#p-35">35</a>.)</p> + +<p>17. Why is continued rain so injurious to wheat, oats, and other grains +before they are mature enough to be harvested? (<a href="#p-35">35</a>; <a href="#exp-32">Exp. 32</a>.)</p> + +<p>18. Would the same effect be likely to occur in the case of very oily +seeds, such as flax and castor beans? Why? (Suggestion: try the effect +of putting water on a piece of oiled paper.)</p> + +<p>19. Explain why many seeds cannot germinate successfully without +air. (<a href="#p-30">30</a>, <a href="#p-31">31</a>; <a href="#exp-25">Exp. 25</a>.)</p> + +<p>20. Mention some of the practical advantages that a farmer, a gardener, +or a careful housewife might gain from experiments like those made in this +section.</p> + +<p>21. Explain why seeds can endure so much greater extremes of temperature +than growing plants. (<a href="#p-23">23</a>, <a href="#p-33">33</a>.)</p> +</div> + + +<h3 id="CH_II_III">III. DEVELOPMENT OF THE SEEDLING</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Seedlings of various kinds in different stages of growth. +It is recommended that the same species be used that were studied in +Section III, Chapter I, or such equivalents as may have been substituted +for them. Enough should be provided to give each pupil three or four +specimens in different stages of development. Seeds, even of the same kind,<span class="pagenum" id="Page_41">[Pg 41]</span> +develop at such different rates that it will probably not be necessary to +make more than two plantings of each sort, from 2 to 5 days apart. +Soaked seeds of corn and wheat will germinate in from 3 to 7 days, +according to the temperature; oats in 1 to 4; beans in 4 to 6; +squash and castor beans in from 8 to 10. Very obdurate ones may +be hastened by clipping. Keep the germinators in an even temperature, +at about 70° to 80° F.</p> + +<p>Pine is a very difficult seed to germinate, requiring usually from 18 to 21 +days. By soaking the mast for twenty-four hours and planting in damp +sand or sawdust kept at an even temperature of 23° C. or about 75° F., +specimens may be obtained.</p> +</div> + +<figure class="figright illowp25" id="i_051" style="max-width: 18.75em;"> + <img class="w100" src="images/i_051.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 54, 55.</span>—Seedling +of corn (<i>after</i> <span class="smcap">Gray</span>): 54, early stage +of germination; 55, later stage.</p></figcaption> +</figure> + +<p id="p-36"><b>36. Seedlings of monocotyls.</b>—Examine a seedling of +corn that has just begun to sprout; from which side does the +seedling spring, the plain or the grooved one? Refer to your +sketch of the dry grain and see if this +agrees with the position of the embryo as +observed in the seed. Make sketches of +four or five seedlings in different stages of +advancement, until you reach one with a +well-developed blade. From what part of +the embryo has each part of the seedling +developed? Which part first appeared +above ground? Is it straight, or bent in +any way? In what direction does the +plumule grow? The hypocotyl? Does the +cotyledon appear above ground at all? Slip +off the husk and see if there is any difference +in the size and appearance of the +contents as you proceed from the younger +to the older plants. How would you account +for the difference?</p> + +<p id="p-37"><b>37. The root.</b>—Examine the lower end of the hypocotyl +and find where the roots originate; would you say that they +are an outgrowth from the stem, or the stem from the root? +Observe that the root of the corn does not continue to grow +in a single main axis like that of the castor bean, but that +numerous adventitious and secondary roots spring from<span class="pagenum" id="Page_42">[Pg 42]</span> +various points near the base of the hypocotyl and spread out +in every direction, thus giving rise to the fibrous roots of +grains and grasses.</p> + +<p id="p-38"><b>38. Root hairs.</b>—Notice the grains of sand or sawdust +that cling to the rootlets of plants grown in a bedding of that +kind. Examine with a lens and see if you +can account for their presence. Lay the root +in water on a bit of glass, hold up to the light +and look for root hairs; on what part are they +most abundant?</p> + +<figure class="figleft illowp10" id="i_52" style="max-width: 19.1875em;"> + <img class="w100" src="images/i_052.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 56.</span>—Seedling +of wheat, with +root hairs.</p></figcaption> +</figure> + +<p>The hairs are the chief agents in absorbing +moisture from the soil. They do not last +very long, but are constantly dying and being +renewed in the younger and tenderer parts of +the root. These are usually broken away in +tearing the roots from the soil, so that it is not +easy to detect the hairs except in seedlings, +even with a microscope. In oat, maple, and radish seedlings +they are very abundant and clearly visible to the naked eye. +The amount of absorbing surface on a +root is greatly increased by their presence.</p> + +<figure class="figright illowp25" id="i_052a" style="max-width: 18.75em;"> + <img class="w100" src="images/i_052a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 57.</span>—Diagrammatic +section of a root +tip: <i>a</i>, cortex; <i>b</i>, central +cylinder in which the +conducting vessels are +situated; <i>c</i>, root cap; <i>g</i>, +growing point.</p></figcaption> +</figure> + +<p id="p-39"><b>39. The root cap.</b>—Look at the tip of +the root through your lens and notice the +soft, transparent crescent or horseshoe-shaped +mass in which it terminates. This +is the root cap and serves to protect the +tender parts behind it as the roots burrow +their way through the soil. Being soft +and yielding, it is not so likely to be injured +by the hard substances with which +it comes in contact as would be the more +compact tissue of the roots. It is composed +of loose cells out of which the solid root +substance is being formed; the growing point of the root, +<i>g</i>, is at the extremity of the tip just behind the cap, <i>c</i> (<a href="#i_052a">Fig. 57</a>). +The cap is very apparent in a seedling of corn, and can easily<span class="pagenum" id="Page_43">[Pg 43]</span> +be seen with the naked eye, especially if a thin longitudinal +section is made. It is also well seen in the water roots of the +common duckweed (<i>Lemna</i>), and on those developed by a +cutting of the wandering Jew, when placed in water. Are +there any hairs on the root cap? Can you account for their +absence?</p> + +<div class="blockquot"> + +<p><span class="smcap">Note.</span>—For a minute study of the structure of roots, see <b><a href="#p-67">67</a></b>.</p> +</div> + +<p id="p-40"><b>40. Organs of vegetation.</b>—The three parts, root, stem, +and leaf, are called organs of vegetation in contradistinction to +the flower and fruit, which constitute +the organs of reproduction. The former +serve to maintain the plant’s individual +existence, the latter to produce +seed for the propagation of the species, +so we find that the seed is both the beginning +and the end of vegetable life.</p> + +<figure class="figright illowp30" id="i_053" style="max-width: 12.5em;"> + <img class="w100" src="images/i_053.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 58.</span>—Seedlings of bean +in different stages of growth: +<i>cc</i>, cotyledons, showing the +plumule and hypocotyl before +germination; <i>a</i>, <i>b</i>, <i>d</i>, and <i>e</i>, +successive stages of advancement. +At <i>d</i> the arch of the +hypocotyl is beginning to +straighten; at <i>e</i> it has entirely +erected itself.</p></figcaption> +</figure> + +<p id="p-41"><b>41. Definitions.</b>—Organ is a general +name for any part of a living thing, +whether animal or vegetable, set apart +to do a certain work, as the heart for +pumping blood, or the stem and leaves +of a plant for conveying and digesting +sap. By “function” is meant the +particular work or office that an organ +has to perform.</p> + +<p id="p-42"><b>42. Seedlings of dicotyls. The bean.</b>—Sketch, without +removing it, a bean seedling that has just begun to show +itself above ground; what part is it that protrudes first? +Sketch in succession four or five others in different stages of +advancement. Notice how the hypocotyl is arched where +it breaks through the soil. Does this occur in the monocotyls +examined? Do the cotyledons of the bean appear above +ground? How do they get out? Can you perceive any +advantage in their being dragged out of the ground backwards +in this way rather than pushed up tip foremost?<span class="pagenum" id="Page_44">[Pg 44]</span> +What changes have the cotyledons undergone in the successive +seedlings? Remove from the earth a seedling just +beginning to sprout and sketch it. From what point does +the hypocotyl protrude through the coats? Does this agree +with its position as sketched in your study of the seed? +In which part of the embryo does the first growth take place?</p> + +<p>Remove in succession the several seedlings you have +sketched and note their changes. How does the root differ +from that of the corn and oats? The first root formed by the +extension of the hypocotyl is the <em>primary</em> root and should be +so labeled in your drawings; the branches that spring from +it are <em>secondary</em> roots. Look for root hairs; if there are +any, where do they occur?</p> + +<figure class="figcenter illowp80" id="i_054" style="max-width: 50em;"> + <img class="w100" src="images/i_054.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 59.</span>—Stages in the germination of a typical seedling of the squash family: +<i>a</i>, a seed before germination; <i>b</i>, <i>c</i>, <i>e</i>, the same in different stages of growth; <i>d</i>, the +empty testa, with kernel removed; <i>hi</i>, hilum; <i>m</i>, micropyle; <i>p</i>, <i>p</i>, the peg in the heel; +<i>h</i>, <i>h</i>, <i>h</i>, the hypocotyl; <i>ar</i>, arch of the hypocotyl; <i>co</i>, cotyledons; <i>pl</i>, plumule; <i>pr</i>, +primary root; <i>sc</i>, secondary roots.</p></figcaption> +</figure> + +<p id="p-43"><b>43. Germination of the squash.</b>—How does the manner +of breaking through the soil compare with that of the bean? +With the corn? From which end of the seed, the large or +the small one, does the hypocotyl spring? Do the cotyledons +come above ground? How do they get out of the seed coat? +Notice the thick protuberance developed by the hypocotyl +and pressing against the lower half of the coat at the point +where the hypocotyl breaks through. This is called the<span class="pagenum" id="Page_45">[Pg 45]</span> +“peg”; can you tell its use? Could the cotyledons get out +of their hard covering without it? Slip the peg below the +coat in one of your growing specimens, leave it in the soil, +and see what will happen. How do the cotyledons of the +squash differ from those of the bean as they come out of the +seed cover? Do they act as foliage leaves? Do you see +any difference in the development of the plumule in the two +seeds (<a href="#i_024a">Figs. 19</a>, <a href="#i_027">25</a>) to account for the different behavior of +the cotyledons? Sketch three seedlings in different stages, +labeling correctly the parts observed. Make a similar study +of the castor bean, or other seedling selected by your teacher, +and illustrate by drawings.</p> + +<p id="p-44"><b>44. Arched and straight hypocotyls.</b>—This difference in +the manner of getting above ground is an important one. +That by means of the arched hypocotyl is, in general, characteristic +of the process of germination in which the cotyledons +come above ground, while the straight kind, which was illustrated +in the corn and wheat, is the prevailing +method when the cotyledons remain +below ground. Can you give a reason for +the difference?</p> + +<figure class="figright illowp25" id="i_055" style="max-width: 29.25em;"> + <img class="w100" src="images/i_055.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 60.</span>—Pine +seedling (<i>After</i> <span class="smcap">Gray</span>).</p></figcaption> +</figure> + +<p id="p-45"><b>45. Polycotyledons; germination of the +pine.</b>—Examine a pine seedling just beginning +to sprout. What part emerges first +from the seed coat? Where does it break +through? Where did you find the micropyle +in the pine seed? (15.) Can you give a +reason why the hypocotyl in seeds should +break through the coats at this point? How +do the cotyledons get out of the testa? Is +the hypocotyl arched or straight in germination? How does +it compare with the bean and squash in this respect? With +the corn? Is any endosperm left in the testa after the cotyledons +have come out? What has become of it? Do the +cotyledons function as leaves? How many of them <a id="tn_45">have</a> the +specimen you are studying? Notice the little knob or button<span class="pagenum" id="Page_46">[Pg 46]</span> +at the upper end of the hypocotyl, just above the point where +the cotyledons are attached; this is the <em>epicotyl</em>, or part +above the cotyledons, here identical with the plumule; does +it develop as rapidly as in the other seedlings you have examined?</p> + +<p id="p-46"><b>46. Relation of parts in the seedling.</b>—Before leaving this +subject, it is important to fix clearly in mind the different +parts of the germinating seedling and their relation to both +the embryo from which they originated and the plant into +which they are to develop. The part labeled “hypocotyl” +in your sketches is all that portion of the embryo below the +point of attachment of the cotyledons. In germination its +upper part will become the stem, and in the embryo constitutes +the <em>caulicle</em>, or stemlet, while its lower part, from +which the root will develop, is the <em>radicle</em>, or rootlet; hence +the term “hypocotyl” includes both the future root and +stem. The plumule is that part of the embryo between the +cotyledons and <em>above</em> their point of attachment to the caulicle. +It is the upward growing point of the young plant, and hence +the place of attachment of the cotyledon is the first <em>node</em>, or +point of leaf origin, on the stem.</p> + +<p>The epicotyl, in contradistinction to the hypocotyl, is all +that part of the plant <em>above</em> the insertion of the cotyledons. +Before germination it is identical with the plumule. As the +seedling grows, the epicotyl advances its growing point by +adding new nodes and <em>internodes</em>, as the spaces between the +successive points of leaf insertion are called.</p> + +<p id="p-47"><b>47. Botanical terms.</b>—As the prefixes <em>hypo</em> and <em>epi</em> are +of frequent occurrence in botanical works, it will aid in +understanding their various compounds if you will remember +that <em>hypo</em> always refers to something below or beneath, +and <em>epi</em>, to something over or above. With this idea in mind +you will see that botanical terms are a labor-saving device, +since it is much easier, in making notes, to use a single descriptive +word than to write out the long English equivalent, +such as “the part under (or over) the cotyledons.”</p> + +<p><span class="pagenum" id="Page_47">[Pg 47]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Do the cotyledons, as a general thing, resemble the mature leaves of +the same plants?</p> + +<p>2. Name some plants in which you have observed differences, and account +for them; could convenience of packing in the seed coats, for instance, +or of getting out of them, have any bearing on the matter?</p> + +<p>3. Does the position in which seeds are planted in the ground have +anything to do with the position of the seedlings as they appear above the +surface?</p> + +<p>4. Is this fact of any importance to the farmer?</p> + +<p>5. Will grain that has begun to germinate make good meal or flour? +Why? (<a href="#p-27">27</a>, <a href="#p-36">36</a>; <a href="#exp-25">Exp. 25</a>.)</p> +</div> + + +<h3 id="CH_II_IV">IV. GROWTH</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Two young potted plants; some lily or hyacinth bulbs; +seedlings of different kinds,—some with well-developed +taproots,—apple, cotton, and maple +are good examples.</p> + +<p><span class="smcap">Appliances.</span>—A small flat dish, some mercury, +and a piece of cork.</p> + +<figure class="figright illowp30" id="i_057" style="max-width: 20.25em;"> + <img class="w100" src="images/i_057.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 61, 62.</span>—Seedling +of corn, marked to +show region of growth: +61, early stage of germination; +62, later stage.</p></figcaption> +</figure> + +<p id="exp-34"><span class="smcap">Experiment 34. How does the root increase +in length?</span>—Mark off the root of a very +young corn seedling into sections by moistening a +piece of sewing thread with indelible ink and +applying it to the surface of the root at intervals +of about two millimeters (⅒ of an inch), or by +tying a thread lightly around it at the same intervals. +Lay the seedling on a moist bedding between +two panes of glass kept apart by a sliver of +wood to prevent their injuring the root by pressure. +Watch for a day or two, and you will see that +growth takes place from a point just back of the +tip (<a href="#i_057">Figs. 61, 62</a>).</p> + +<p>Mark off a seedling of the bean in the same +way and watch to see whether it increases in the same manner as the corn.</p> + +<p id="exp-35"><span class="smcap">Experiment 35. How does the stem increase in length?</span>—Mark +off a portion of the stem of a bean seedling as explained in the last experiment, +and find out how it grows. Allow a seedling to develop until it +has put forth several leaves and measure daily the spaces between them. +Label these spaces in your drawings, “internodes,” and the points where the +leaves are attached, “nodes.” Does an internode stop growing when the<span class="pagenum" id="Page_48">[Pg 48]</span> +one next above it has formed? When is growth most rapid? Reverse the +position of a number of seedlings that have just begun to sprout and watch +what will happen. After a few days reverse again and note the effect.</p> + +<figure class="figcenter illowp100" id="i_058x" style="max-width: 40em;"> + <img class="w100" src="images/i_058x.jpg" alt=""> + <figcaption> +<table class="autotable"> +<tr> +<td class="tdl wd50"><p><span class="smcap">Figs.</span> 63, 64.—Root of bean seedling, measured to show region of growth: 63, +early stage of germination; 64, later stage.</p></td> +<td class="tdl"><p><span class="smcap">Figs.</span> 65, 66.—Stem of bean seedling, measured to show region of growth: 65, +early stage of growth; 66, later stage.</p></td> +</tr> +</table> +</figcaption> +</figure> + +<p id="exp-36"><span class="smcap">Experiment 36. Can plants grow and lose weight at the same +time?</span>—Remove the scales from a white +lily bulb, weigh them, and lay in a warm, +but not too damp place, away from the +light. After a time bulblets will form at +the bases of the scales. Weigh them again, +and if there has been any loss, account +for it. The experiment may be tried by +allowing a potato tuber or a hyacinth bulb +to germinate without absorbing moisture +enough to affect its weight.</p> + +<figure class="figleft illowp30" id="i_058" style="max-width: 29.75em;"> + <img class="w100" src="images/i_058.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 67, 68.</span>—Experiment showing +the direction of growth in stems: +67, young potato planted in an inverted +position; 68, the same after +an interval of eight days.</p></figcaption> +</figure> + +<p id="exp-37"><span class="smcap">Experiment 37. Is the direction of +growth a matter of any importance?</span>—Plant +in a pot suspended as shown in +<a href="#i_058">Fig. 67</a>, a healthy seedling of some kind, +two or three inches high, so that the +plumule shall point downward through +the drain hole and the root upward into +the soil. Watch the action of the stem<span class="pagenum" id="Page_49">[Pg 49]</span> +for six or eight days, and sketch it at successive intervals. After the stem +has directed itself well upward, invert the pot again, and watch the growth. +After a week remove the plant and notice the direction of the root. Sketch +it entire, showing the changes in direction of growth.</p> + +<p>At the same time that this experiment is arranged, lay another pot with a +rapidly growing plant on one side, and every forty-eight hours reverse the +position of the pot, laying it on the opposite side. At the end of ten or +twelve days remove the plant and examine. How has the growth of root +and stem been affected?</p> + +<p>What do we learn from these experiments and from <a href="#exp-35">Exp. 35</a> as to the +normal direction of growth in these two organs respectively? Can you +think of any natural force that might influence this direction?</p> + +<figure class="figright illowp30" id="i_059" style="max-width: 20em;"> + <img class="w100" src="images/i_059.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 69.</span>—Experiment +showing the root of a seedling +forcing its way downward +through mercury.</p></figcaption> +</figure> + +<p id="exp-38"><span class="smcap">Experiment 38. To show that plants will exert force rather +than change their direction of growth.</span>—Pin a sprouted bean to a +cork and fasten the cork to the side of a flat dish, +as shown in <a href="#i_059">Fig. 69</a>. Cover the bottom of the dish +with mercury at least half an inch deep, and over +the mercury pour a layer of water. Cover the +whole with a pane of glass to keep the moisture in, +and leave for several days. The root will force its +way downward into the mercury, although the +latter is fourteen times heavier than an equal +bulk of the bean root substance, and the root must thus overcome a +resistance equal to at least fourteen times its own weight.</p> +</div> + +<p id="p-48"><b>48. What growth is.</b>—With the seedling begins the +growth of the plant. Most people understand by this +word mere increase in size; but growth is something more +than this. It involves a change of form, usually, but not +necessarily, accompanied by increase in bulk. Mere mechanical +change is not growth, as when we bend or stretch +an organ by force, though if it can be kept in the altered +position till such position becomes permanent, or as we say +in common speech, “till it grows that way,” the change +may become growth. To constitute true growth, the change +of form must be permanent, and brought about, or maintained, +by forces within the plant itself.</p> + +<p id="p-49"><b>49. Conditions of growth.</b>—The internal conditions depend +upon the organization of the plant. The essential +external conditions are the same as those required for germination:<span class="pagenum" id="Page_50">[Pg 50]</span> +food material, water, oxygen, and a sufficient +degree of warmth. It may be greatly influenced by other +circumstances, such as light, gravitation, pressure, and +(probably) electricity; but the four first named are the essential +conditions without which no growth is possible.</p> + +<p id="p-50"><b>50. Cycle of growth.</b>—When an organ becomes rigid +and its form fixed, there is no further growth, but only nutrition +and repair,—processes which must not be confounded +with it. Every plant and part of a plant has its period of +beginning, maximum, decline, and cessation of growth. The +cycle may extend over a few hours, as in some of the fungi, or, +in the case of large trees, over thousands of years.</p> + +<p id="p-51"><b>51. Geotropism.</b>—The general tendency of the growing +axes of plants to take an upward and downward course as +shown in <a href="#exp-37">Exp. 37</a>—in other words, to point to and from the +center of the earth—is called <em>geotropism</em>. It is <em>positive</em> when +the growing organs point downward, as most primary roots +do; <em>negative</em> when they point upward, as in most primary +stems; and <em>transverse</em>, or <em>lateral</em>, when they extend horizontally, +as is the case with most secondary roots and branches.</p> + +<p id="p-52"><b>52. Gravity and growth.</b>—It cannot be proved directly +that geotropism is due to gravity, because it is not possible +to remove plants from its influence so as to see how they +would behave in its absence. The effect of gravity may be +neutralized, however, by arranging a number of sprouting +seeds on the vertical disk of a clinostat, an instrument +fitted with a clockwork movement by means of which they +may be kept revolving steadily for several days. By this +constant change of position gravity is made to act on them +in all directions alike, which is the same in some respects as +if it did not act at all. If the disk is made to revolve +rapidly, the growing root tips turn toward the axis of motion, +without showing a tendency to grow downward. We may +then conclude that geotropism is a reaction to gravity.</p> + +<p id="p-53"><b>53. Geotropism an active force.</b>—It must be noted, +however, that the force here alluded to is not the mere mechanical<span class="pagenum" id="Page_51">[Pg 51]</span> +effect of gravity, due to weight of parts, as when the +bough of a fruit tree is bent under the load of its crop, but +a certain stimulus to which the plant reacts by a spontaneous +adjustment of its growing parts. In other words, geotropism +is an active, not a passive function, and the plant will +overcome considerable resistance in response to it. (<a href="#exp-38">Exp. 38</a>).</p> + +<p id="p-54"><b>54. Other factors.</b>—The direction of growth is influenced +by many other factors, such as light, heat, moisture, +contact with other bodies, and perhaps by +electricity. The result of all these forces is an +endless variety in the forms and growth of +organs that seems to defy all law.</p> + +<figure class="figcenter illowp100" id="i_061" style="max-width: 30em;"> + <img class="w100" src="images/i_061.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 70.</span>—A piece of a haulm of millet that has been laid horizontally, righting +itself through the influence of negative geotropism.</p></figcaption> +</figure> + +<p>Heat, unless excessive, generally stimulates +growth; contact sometimes stimulates it, +causing the stem to curve away from the disturbing +object, and sometimes retards it, causing +the stem to curve toward the object of contact +by growing more rapidly on the opposite side, +as in the stems of twining vines. Light stimulates nutrition, +but generally retards growth. The movements of plants +toward the light are effected in this way; growth being +checked on that side, the plant bends toward the light.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why do stems of corn, wheat, rye, etc., straighten themselves after +being prostrated by the wind? (<a href="#p-51">51</a>, <a href="#p-54">54</a>.)</p> + +<p>2. Do plants grow more rapidly in the daytime, or at night? (<a href="#p-54">54</a>.)</p> + +<p>3. Reconcile this with the fact that green plants will die if deprived +of light.</p> + +<p><span class="pagenum" id="Page_52">[Pg 52]</span></p> + +<p>4. Which grows more rapidly, a young shoot or an old one? (<a href="#p-31">31</a>, <a href="#p-50">50</a>.)</p> + +<p>5. Which, as a general thing, are the more rapid growers, annuals or +perennials? Herbaceous or woody-stemmed plants?</p> + +<p>6. Name some of the most rapid growers you know.</p> + +<p>7. Of what advantage is this habit to them?</p> + +<p>8. Why do roots form only on the under side of subterraneous stems? +(<a href="#p-51">51</a>.)</p> + +<p>9. Why do new twigs develop most freely on the upper side of horizontal +branches? (<a href="#p-51">51</a>.)</p> +</div> + + +<h4 id="CH_II_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>(1) Notice the various seedlings met with in your walks and see how +many you can recognize by their resemblance to the mature plants. Account +for any differences you may observe between seedlings and older +plants of the same species. Observe the cotyledons as they come up and +their manner of getting out of the ground, and notice the ways in which +this is influenced by moisture, light, and the nature of the soil. Where +the cotyledons do not appear, dig into the ground and find out the reason. +Notice which method of emergence occurs in each case, the arched, or +straight, and account for it. Observe particularly the behavior of seedlings +in hard, sunbaked soil. If you see any of them lifting cakes of earth, +compare the size and weight of the cake with that of the seed; if there is +any disparity, what does this imply? What is the force called which the +plant exercises in lifting the weight? (51.)</p> + +<p>(2) Notice if there are any seeds germinating successfully on top of +the ground, and find out by what means their roots get into the soil. +Observe what effect sun and shade, moisture and drought, and the nature +of the soil have on the process. Find out whether roots exercise force in +penetrating the soil; what kinds they penetrate most readily, and what +kinds, if any, they fail to penetrate at all. Notice whether seedlings with +taproots, like the turnip and castor bean, or those with fibrous roots, like +corn and wheat, are more successful in working their way downward.</p> + +<p>(3) Look for tree seedlings. Explain why seedlings of fruit trees are so +much more widely distributed in cultivated districts, and so much easier +to find than those of forest trees. Where do the latter occur, as a general +thing? Account for the fact that seedling trees are so much more rare +than germinating herbs, and why trees like the oak and chestnut and +black walnut propagate so much more slowly, in a state of nature, than +the pine, cedar, ash, and maple.</p> + +<p>(4) Observe the direction of growth in plants on the sides of gullies and +ravines, and tell how it is influenced by geotropism. Notice whether there +are other influences at work; for instance, light, or in the case of roots, +the attraction of moisture.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_53">[Pg 53]</span></p> + +<h2 class="nobreak" id="CH_III">CHAPTER III. THE ROOT</h2> +</div> + + +<h3 id="CH_III_I">I. OSMOSIS AND THE ACTION OF THE CELL</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For experiments in osmosis provide fresh and boiled +slices of red beet, a fresh egg, a piece of ox bladder or some parchment +paper; glass tubing, thread, twine, elastic bands, salt and sugar solutions. +A common medicine dropper with the small end cut off will answer instead +of tubing for making an artificial cell; or an eggshell may be used, by +blowing out the contents through a puncture in the small end, and carefully +chipping away a portion of the shell at the big end, leaving the lining +membrane intact. The different liquids can be put into the shell and the +exposed membrane placed in contact with the liquid +in the glass, by fitting over the latter a piece of cardboard +with a hole in the center large enough for the +exposed surface to protrude sufficiently to touch the +water.</p> +</div> + +<figure class="figright illowp25" id="i_063" style="max-width: 14.75em;"> + <img class="w100" src="images/i_063.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 71.</span>—Artificial +cell.</p></figcaption> +</figure> + +<p id="p-55"><b>55. Object of the experiments.</b>—In order +to understand clearly the action of roots +in absorbing nutrients from the soil, it will +be necessary to learn something about the +movement of liquids through the cells, upon +which the physiological processes of the +plant depend. For this purpose make an +artificial cell by tying a piece of ox bladder +or parchment paper tightly over one end of +a small glass tube, as shown in <a href="#i_063">Fig. 71</a>.</p> + +<div class="blockquot"> + +<p id="exp-39"><span class="smcap">Experiment 39. How does absorption take +place in the cell?</span>—(<i>a</i>) Put some salt water in +a wineglass, partly fill the tube of the artificial cell +with fresh water, and mark on the outside of both +vessels the height at which the contained liquid stands. Set the tube +in the glass of salt water and wait for results, having first tested carefully +to make sure that there are no leaks in the membrane. After half +an hour, notice whether there is any increase of water in the glass, as +indicated by the mark. If so, where did it come from? Is there any loss<span class="pagenum" id="Page_54">[Pg 54]</span> +of water in the tube? What has become of it? How did it get out? +Taste it to see if any of the salt water has got in. Which is the heavier, +salt water, or fresh? (If you do not know, weigh an equal quantity of +each.) In which direction did the principal flow take place; from the +heavier to the lighter, or from the lighter to the heavier liquid?</p> + +<p>(<i>b</i>) Put a sugar or salt solution in the tube, and clear, fresh water in +the glass, marking the height in each as before. Does the liquid rise or +fall in the tube? Does any of it escape into the water of the glass, and if +so, is it more or less than before? Which now contains the denser fluid, +the tube or the glass? What principle governs the course of the liquid? +Try the same experiment with (<i>c</i>), the same liquid in both vessels, and +notice whether there is a greater flow in one direction than the other, as +indicated by a comparison with the marks on the outside. (<i>d</i>) Put in +the tube some of the white of a raw egg, insert in a glass of pure water, and +note the effect. (<i>e</i>) Reverse, with water in the tube and white of egg +in the glass. Does the water rise in the tube as before? Test the contents +for proteins; has any of the albumin passed through the membrane into +the tube?</p> + +<p id="exp-40"><span class="smcap">Experiment 40. To test the behavior of living and dead cells.</span>—Slice +a fresh piece of red beet into a vessel of water and of a boiled one into +another vessel of the same liquid at the same temperature. What difference +do you notice? Can you think of any reason why the boiled one gives +up its juices and the other one does not?</p> +</div> + +<p id="p-56"><b>56. Osmosis.</b>—The passage of liquids or of solids in solution +through membranes is known as <em>osmosis</em>. Our experiments +have shown that the principles governing the osmotic +movement are: (1) the passage of water from the thinner +liquid toward the denser takes place more rapidly than in +the opposite direction; (2) the rapidity of the transfer depends +on the difference in density; (3) crystallizable substances +in solution, like sugar and salt, osmose readily; +(4) albuminous or gelatinous substances, such as the white +of an egg, osmose so slowly that the cell wall may be regarded +as practically impermeable to them.</p> + +<p id="p-57"><b>57. Osmosis a form of diffusion.</b>—Osmosis is related to +diffusion as a part to the whole. In other words, it is a name +given to the process when it takes place through a membrane, +whether solid, as the outer wall of the cell, or semi-fluid, +as the inner wall of living protoplasm. Diffusion may<span class="pagenum" id="Page_55">[Pg 55]</span> +therefore take place without osmosis, that is, in the absence +of a membrane, as, for example, when we sweeten our tea or +coffee by allowing sugar to diffuse through it. Many membranes +offer little resistance to the osmotic movement of +crystallizable substances. Such membranes are said to be +<em>permeable</em>. Membranes which are not permeable to the dissolved +solids, are called <em>semi-permeable</em>, since they allow the +diffusion of water but not of the substances in solution. +Living protoplasm is of this class. It is only very slightly +permeable to many substances toward which, when dead, it +acts as a permeable membrane.</p> + +<p id="p-58"><b>58. Absorption in living and dead cells.</b>—There is one +great difference between the action of the artificial cell used +in the foregoing experiments and that of the cells of which +a living body is built up. The living cell always has at least +two membranes. One of these, the cell wall, is readily permeable, +while the other, the protoplasm, is semi-permeable—that +is, substances in solution usually diffuse more or less +slowly, while water diffuses rapidly. Hence in the living cell +the protoplasm exercises a power of absorption independent +of the cell wall, sometimes rejecting substances admitted by +the latter, sometimes retaining others to which it is permeable, +as shown in <a href="#exp-40">Exp. 40</a>. In the boiled beet the protoplasm +had been killed and the red coloring matter passed through +it unhindered, while in the living one it was held back +by the protoplasmic lining, which is thus seen to control the +absorptive properties of the cell.</p> + +<p id="p-59"><b>59. Plasmolysis.</b>—Cells can be killed or injured in other +ways than by heat; for example, by cold, by poisons, by +starvation, and by overfeeding through the use of too much +fertilizer or too rich a one. In this last case, the soil water +becomes impregnated with soluble matter from the manure, +which may render it denser than the sap in the roots. When +this happens, it will cause the osmotic flow to set outward +and thus deplete the cell of its water; whence we have +the paradox that a cell, or even a whole plant, may be starved<span class="pagenum" id="Page_56">[Pg 56]</span> +by overfeeding. This action of osmosis in withdrawing +the contents from a cell is termed <em>plasmolysis</em>, and you can +easily understand how very important a knowledge of the +principles governing it is to the farmer in determining the +application of fertilizers to his crops.</p> + +<p>Dead cells, although powerless to carry on the life processes +of a plant, have nevertheless important uses in serving the +purposes of mechanical support and also to some extent in +assisting in the work of absorption, though their function +here is a purely mechanical one.</p> + +<figure class="figright illowp60" id="i_066" style="max-width: 51.0625em;"> + <img class="w100" src="images/i_066.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 72.</span>—Root of a tree enveloping a rock. +The large sycamore, whose base is partly concealed +by the trumpet creeper on the left of the picture, +is growing in very hard, stony soil, and one of +its main roots has molded itself so completely to the +ledge of rock protruding on the right, that when a +portion of it was torn away, as shown where the light +streak ends at <i>a</i>, the impress of its fibers was so +strongly marked on the rock as to give the latter the +appearance of a petrified root.</p></figcaption> +</figure> + +<p id="p-60"><b>60. Selective absorption.</b>—Different plants through +their roots absorb different substances from the soil water, or +the same substance +in varying degrees. +Hence, one kind of +crop will exhaust +the soil of certain +minerals while leaving +other kinds intact, +or very little +diminished; and <i>vice +versa</i>, another kind +will take up abundantly +what its predecessor +has rejected. +In this sense, plants +are said to exercise a +selective power in +the absorption of nutrients. +The expression +must not be understood, however, as implying any kind +of volitional discrimination. It is merely a short and convenient +way of saying that the cells of different plants possess +different degrees of permeability to certain substances, some +being more permeable to one thing, some to another. But +beyond this rejection of untransmissible substances there is no<span class="pagenum" id="Page_57">[Pg 57]</span> +active power of discrimination, any substance that can pass +through the cell wall and its protoplasmic lining being taken +in, whether useful, unnecessary, or even harmful. These may, +however, be got rid of by excretion, as the superfluous water +taken in with dissolved minerals is exhaled from the leaves; +or if incapable of passing out by osmosis, rendered harmless +and retained in the +form of the curious +“crystalloids” found +in various parts of +plants. But while +the kind of selection +exercised by vegetable +cells implies no +power of choice, as a +matter of fact those +substances most +used by the plant in +carrying on its life +processes are absorbed +in much +greater quantities +than others, being +transferred to parts +where growth or +other changes in the +plant tissues are going +on, and there +used up in the work of nutrition, or excreted in part as waste +products. In either case their passage from cell to cell will +give rise to a continuous osmotic current in that direction, +and the absorption of new matter will go on in proportion to +the amounts used up.</p> + +<figure class="figcenter illowp50" id="i_067" style="max-width: 38.75em;"> + <img class="w100" src="images/i_067.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 73.</span>—Roots of elm and sycamore contending for +possession of the soil on a rocky bluff on the Potomac.</p></figcaption> +</figure> + +<p id="p-61"><b>61. Definition.</b>—Tissue is a word used to denote any +animal or vegetable substance having a uniform structure +organized to perform a particular office or function. Thus,<span class="pagenum" id="Page_58">[Pg 58]</span> +for instance, we have bony tissue and muscular tissue in +animals; that is, tissue made of bone substance and muscle +substance and doing the work of bone and muscle respectively. +Likewise in plants, we have strengthening tissue +made up of hard, thick-walled cells, serving mainly for purposes +of mechanical support, and vascular tissue, made up of +conducting vessels for conveying sap—and so on, for every +separate function.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why do raspberries and strawberries have a flabby, wilted look if +sugar has been put on them too long before they are served? (<a href="#p-7">7</a>, <a href="#p-56">56</a>.)</p> + +<p>2. Where has the juice gone? What caused it to go out of the berries? +(<a href="#p-56">56</a>, <a href="#p-59">59</a>.)</p> + +<p>3. Is a knowledge of the principles governing osmosis of any practical +use to the housekeeper?</p> + +<p>4. Why cannot roots absorb water as freely in winter as in summer? +(Suggestion: which is the heavier, cold or warm water?)</p> + +<p>5. Why does fertilizing too heavily sometimes injure a crop? (<a href="#p-59">59</a>.)</p> + +<p>6. Do you see any apparent contradiction between the action of plasmolysis +and the selective power of protoplasm? Can you reconcile it?</p> + +<p>7. If a piece of beet that has been frozen is placed in water it will behave +just as the slice of boiled beet did in <a href="#exp-40">Exp. 40</a>; explain. (<a href="#p-58">58</a>, <a href="#p-59">59</a>.)</p> +</div> + + +<h3 id="CH_III_II">II. MINERAL NUTRIMENTS ABSORBED BY PLANTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A dozen or two each of different kinds of seeds and grains. +A small portion from a growing shoot of a woody and a herbaceous land +plant, and of some kind of succulent water or marsh plant, such as arrow +grass (<i>Sagittaria</i>), water plantain, etc.</p> + +<p><span class="smcap">Appliances.</span>—A pair of scales; a lamp, stove, or other means of burning +away the perishable parts of the specimens to be studied.</p> + +<p id="exp-41"><span class="smcap">Experiment 41.—Do the tissues of plants contain mineral +matter?</span>—Take about a dozen each of grains and seeds of different kinds, +weigh each kind separately, and then dry them at a high temperature, but +not high enough to scorch or burn them. After they have become perfectly +dry, weigh them again. What proportion of the different seeds was water, +as indicated by their loss of weight in drying?</p> + +<p>Burn all the solid part that remains, and then weigh the ash. What +proportion of each kind of seed was of incombustible material? What +proportion of the solid material was destroyed by combustion?</p> + +<p><span class="pagenum" id="Page_59">[Pg 59]</span></p> + +<p id="exp-42"><span class="smcap">Experiment 42.—Do they contain different kinds and quantities +of minerals?</span>—Test in the same way the fresh, active parts of any +kind of ordinary land plant (sunflower, hollyhock, pea vines, etc.), and +of some kind of succulent water or marsh plant (Sagittaria, water lily, +fern). Do you notice any difference in the amount of water given off and +of solid matter left behind? In the character of the ashes left? Have +you observed in general any difference between the ashes of different +woods; as, for instance, hickory, pine, oak? Compare with the residue +left in <a href="#exp-21">Exp. 21</a>; would you judge that the residual substances are of the +same composition?</p> +</div> + +<figure class="figright illowp30" id="i_069" style="max-width: 19.75em;"> + <img class="w100" src="images/i_069.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 74.</span>—Water cultures +of buckwheat, showing +effect of the lack of the +different food elements: +1, with all the elements; +2, without potassium; 3, +with soda instead of potash; +4, without calcium; +5, without nitrates or ammonia +salts.</p></figcaption> +</figure> + +<p id="p-62"><b>62. Essential constituents.</b>—The composition of the +ash of any particular plant will depend upon two things: +the absorbent capacity of the plant itself +and the nature of the substances contained +in the soil in which it grows. But +chemical analysis has shown that however +the ashes may vary, they always +contain some proportion of the following +substances: potassium (potash), +calcium (lime), magnesium, phosphorus, +and (in green plants) iron. These elements +occur in all plants, and if any one +of them is absent, growth becomes abnormal +if not impossible.</p> + +<p>The part of the dried substances that +was burned away after expelling the +water consists, in all plants, mainly of +carbon, hydrogen, oxygen, nitrogen, and +sulphur, in varying proportions. These +five rank first in importance among the +essential elements of vegetable life, and +without them the plant cell itself, the physiological unit of +vegetable structure, could not exist. They compose the +greater part of the substance of every plant, carbon alone +usually forming about one half the dry weight. Other substances +may be present in varying proportions, but the two +groups named above are found in all plants without exception,<span class="pagenum" id="Page_60">[Pg 60]</span> +and so we may conclude that (with the possible addition +of chlorine) they form the indispensable elements of plant +food. Carbon, hydrogen, oxygen, nitrogen, sulphur, and +phosphorus compose the structure of which the plant is built. +The other four ingredients do not enter into the substance as +component parts, but aid in the chemical processes by which +the life functions of the plant are carried on, and are none +the less essential elements of its food. <a href="#i_069">Figure 74</a> shows the +difference between a plant grown in a solution where all +the food elements are present, and others in which some of +them are lacking.</p> + +<figure class="figright illowp40" id="i_070" style="max-width: 39.0625em;"> + <img class="w100" src="images/i_070.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 75.</span>—Roots of soy bean bearing +tubercle-forming bacteria.</p></figcaption> +</figure> + +<p id="p-63"><b>63. How plants obtain their food material.</b>—Plants +obtain their supply of the various mineral salts from solutions +in the soil water which +they absorb through their +roots. With a few doubtful +exceptions, they cannot assimilate +their food unless it +is in a liquid or gaseous form. +Of the gases, carbon dioxide, +oxygen, and hydrogen can +be freely absorbed from the +air, or from water with various +substances in solution, +but most plants are so constituted +that they cannot absorb free nitrogen from the air; +they can take it only in the form of compounds from nitrates +dissolved in the soil, and hence the importance of ammonia +and other nitrogenous compounds in artificial fertilizers. +Some of the pea family, however, bear on their roots little +tubers formed by minute organisms called bacteria, which +have the power of extracting nitrogen directly from the +free air mingled with the soil; and hence the soil in which +these tuber-bearing legumes decay is enriched with nitrogen +in a form ready for use.</p> + +<p><span class="pagenum" id="Page_61">[Pg 61]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Could any normal plant grow in a soil from which nitrogen was lacking? +Potash? Lime? Phosphorus? (<a href="#p-62">62</a>.)</p> + +<p>2. Could it live in an atmosphere devoid of oxygen? Nitrogen? Carbon +dioxide? (<a href="#p-62">62</a>.)</p> + +<p>3. Why are cow peas or other legumes planted on worn-out soil to renew +it? (<a href="#p-63">63</a>.)</p> + +<p>4. Is the same kind of fertilizer equally good for all kinds of soil? For +all kinds of plants? (<a href="#p-60">60</a>, <a href="#p-62">62</a>.)</p> + +<p>5. Why does too much watering interfere with the nourishment of +plants? (<a href="#exp-26">Exps. 26</a>, <a href="#exp-27">27</a>.)</p> + +<p>6. Are ashes fit for fertilizers after being leached for lye? (<a href="#p-62">62</a>.)</p> + +<p>7. Why will plants die, or make very slow growth, in pots, unless the +soil is renewed occasionally? (<a href="#p-60">60</a>, <a href="#p-62">62</a>.)</p> +</div> + + +<h3 id="CH_III_III">III. STRUCTURE OF THE ROOT</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Taproot of a young woody plant not over one or two +years old; apple and cherry shoots make good specimens. For showing +root hairs, seedlings of radish, turnip, or oat are good, also roots of wandering +Jew grown in water; for the rootcap, corn, sunflower, squash.</p> +</div> + +<figure class="figright illowp40" id="i_071" style="max-width: 33.5em;"> + <img class="w100" src="images/i_071.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 76.</span>—Cross section of a young +taproot; <i>a</i>, <i>a</i>, root hairs; <i>b</i>, epidermis; +<i>c</i>, cortical layer; <i>d</i>, fibrovascular +cylinder. Note the absence of medullary +rays during the first year of +growth.</p></figcaption> +</figure> + +<p id="p-64"><b>64. Gross anatomy of the root.</b>—Cut a cross section of +any woody taproot, about halfway between the tip and the +ground level, examine it with a lens, and sketch. Label +the dark outer covering, <em>epidermis</em>, the soft layer just within +that, <em>cortex</em>, the hard, woody axis +that you find in the center, <em>vascular +cylinder</em>, and the fine silvery +lines that radiate from the +center to the cortex, <em>medullary +rays</em> (in a very young root these +will not appear). Cut a section +through a root that has stood in +coloring fluid for about three +hours and note the parts colored +by the fluid. What portion of +the root, would you judge from +this, acts as a conductor of the +water absorbed from the ground?</p> + +<p><span class="pagenum" id="Page_62">[Pg 62]</span></p> + +<p>Make a longitudinal section passing through the central +portion of the root and extending an inch or two into the +lower part of the stem. Do you find any sharp line of division +between them? Notice the hard, woody axis that runs +through the center. This is the vascular cylinder and contains +the conducting vessels, the cut ends of which were +shown in cross section in <a href="#i_071">Fig. 76</a>.</p> + +<figure class="figright illowp20" id="i_072" style="max-width: 25em;"> + <img class="w100" src="images/i_072.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 77.</span>—Verti-section +of branching +root, showing the +branches, <i>n</i>, <i>n</i>, originating +in the central +axis, <i>f</i>, and passing +through the cortex, +<i>r</i>, <i>r</i>.</p></figcaption> +</figure> + +<p id="p-65"><b>65. Distinctions between root and stem.</b>—Pull off a +branch from the stem and one from the root; which comes +off the more easily? Examine the points of +attachment of the two and see why this is so. +This mode of branching from the central +axis instead of from the external layers, as +in the stem, is one marked distinction between +the structure of the two organs. In +stems, moreover, branches occur normally +above the points of leaf insertion at the +nodes <a href="#p-46">(46)</a>, while in the root they tend to +arrange themselves in straight vertical rows. +The shoots and cions that often originate +from them are not normal root branches, +but outgrowths from irregular or <em>adventitious</em> buds, that +may occur on any part of a plant. The root is not divided +into nodes like the stem, +and never bears leaves.</p> + +<figure class="figright illowp40" id="i_072a" style="max-width: 38.6875em;"> + <img class="w100" src="images/i_072a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 78.</span>—Root of a tree on the side of +a gulley, acting as stem.</p></figcaption> +</figure> + + +<p id="p-66"><b>66. The active part of +the root.</b>—It is only the +newest and most delicate +parts of the root that produce +hairs and are engaged +in the active work of absorption, +the older parts acting +mainly as carriers. Hence, +old roots lose much of their +characteristic structure and +take on more and more of<span class="pagenum" id="Page_63">[Pg 63]</span> +the office of the stem, until there is practically no difference +between them. On the sides of gullies, where the earth +has been washed from around the trees, we often see the +upper portion of the root covered with a thick bark and fulfilling +every office of a true stem.</p> + +<p id="p-67"><b>67. Minute structure of the root.</b>—(<i>a</i>) Mount in water +and place under the microscope a portion of the root of an +oat or radish seedling containing a number of hairs. In +studying the thin, transparent roots of very young seedlings +a section will not be necessary. Observe whether the hairs +originate from the epidermis or +from the interior. Are they true +roots, or mere outgrowths from +the cells of the epidermis? Do +they consist of a single cell or a +number of cells each? Notice +what very thin cell walls the +hairs have; is there any advantage +in this? The interior, transparent +portion of the hair contains +the sap, and the protoplasm +forms a thin lining on the inner +surface of the wall; why not +the sap next the wall and the +protoplasm in the interior? (<a href="#p-58">58</a>, +<a href="#p-60">60</a>.)</p> + +<figure class="figright illowp30" id="i_073" style="max-width: 32.75em;"> + <img class="w100" src="images/i_073.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 79.</span>—Longitudinal section +through the tip of a young root, somewhat +diagrammatic: <i>h</i>, <i>h</i>, root hairs; +<i>ep</i>, epidermis; <i>a</i>, cortex; <i>b</i>, central +cylinder; <i>e</i>, sheath of the cylinder +(endodermis); <i>g</i>, growing point; <i>c</i>, +root cap; <i>d</i>, dead and dying cells loosened +from the extremity of the cap.</p></figcaption> +</figure> + +<p>(<i>b</i>) Next examine a portion +of the body of the root and try to make out the parts as +shown in <a href="#i_073">Fig. 79</a>, and compare them with your observations +in 64. The light line running through the middle is +the <em>central cylinder</em>, up which the water passes, as was shown +by the colored liquid in 64. Outside this is a darker portion +(<i>a</i>, <a href="#i_073">Fig. 79</a>), corresponding to the cortex (<i>rr</i>, <a href="#i_072">Fig. 77</a>). +Besides other uses, the cortex serves to prevent the loss +of water as it passes up to the stem, and also, in fleshy +roots like the carrot and turnip, for the storage of nourishment.<span class="pagenum" id="Page_64">[Pg 64]</span> +Its innermost row of cells is thickened into the +sheath, or <em>endodermis</em> (<i>e</i>), which serves as an additional +protection to the conducting tissues. The extreme outer +layer, from the cells of which the root hairs are developed, +is, as already stated, the epidermis, and in the older and +more exposed parts of perennial roots is displaced by the +bark, which becomes indistinguishable from that of the +stem. (66.)</p> + +<p>(<i>c</i>) Look at the tip of the root for a loose structure (<i>c</i>) +fitting over it like a thimble. This is the rootcap. Do you +see any loose cells that seem to have broken away from it? +These are old cells that have been pushed to the front by +the formation of new growth back of them, and, being of no +further use, are rubbed off by friction as the root bores its +way through the soil. Draw a longitudinal section of the +root as it appears under the microscope, labeling all the parts. +If they cannot be made out distinctly in the specimen examined, +use sections of young corn or bean roots, which are +larger and show the parts more distinctly.</p> + +<figure class="figleft illowp30" id="i_074" style="max-width: 33.5em;"> + <img class="w100" src="images/i_074.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 80.</span>—Cross section of a young root, +magnified: <i>h</i>, hairs; <i>a</i>, cortex; <i>b</i>, central +cylinder; <i>e</i>, sheath or endodermis; <i>ep</i>, epidermis; +<i>sp</i>, cut ends of the ducts.</p></figcaption> +</figure> + +<p>(<i>d</i>) Place under the microscope a thin cross section +through the hairy portion of a primary root of a bean or pea +seedling, and try to make +out the parts noted above +and shown in cross section in +<a href="#i_074">Fig. 80</a>. Make a sketch of +what you see, labeling all +the parts you can recognize. +Show in your drawing the +differences in the size and +shape of the cells composing +the different tissues. Notice +in the central cylinder +(<a href="#i_074">Fig. 80</a>) several groups of +what look in the section like +little round pits, or holes, <i>sp</i>. These are the cut ends of +large-sized tubes or <em>ducts</em> that convey the water absorbed<span class="pagenum" id="Page_65">[Pg 65]</span> +by the roots to the stem. Each set of these tubes, together +with a number of smaller ones belonging to the same group, +constitutes a <em>fibrovascular bundle</em>—a very important element +in the structure of all roots and stems, as these bundles +make up the conducting system of the plant body.</p> + + +<h3 id="CH_III_IV">IV. THE WORK OF ROOTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Germinating seedlings of radish, bean, corn, etc.; a +potted plant of calla, fuchsia, tropæolum, touch-me-not (<i>Impatiens</i>), or +corn; a plant that has been growing for some time in a porous earthen +jar.</p> + +<p><span class="smcap">Appliances.</span>—Glass tumblers; coloring fluid; wax; some coarse netting; +dark wrapping paper, or a long cardboard box; a sheet of oiled +paper; some half-inch glass tubing; a few inches of rubber tubing; an +ounce of mercury; some blue litmus paper; a flower pot full of earth; +a few handfuls of sand, clay, and vegetable mold; a pair of scales; a +half dozen straight lamp chimneys, or long-necked bottles from which +the bottoms have been removed as directed in <a href="#exp-53">Exp. 53</a>.</p> + +<p id="exp-43"><span class="smcap">Experiment 43. Use of the epidermis.</span>—Cut away the lower end +of a taproot; seal the cut surface with wax so as to make it perfectly +water-tight, and insert it in red ink for at least half the remaining length, +taking care that there is no break in the epidermis. Cut an inch or two +from the tip of the lower piece, or if material is abundant, from another +root of the same kind, and without sealing the cut surface, insert it in red +ink, beside the other. At the end of three or four hours, examine longitudinal +sections of both pieces. Has the liquid been absorbed equally by +both? If not, in which has it been absorbed the more freely? What conclusion +would you draw from this, as to the passage of liquids through +the epidermis?</p> + +<p>From this experiment we see that the epidermis, besides protecting the +more delicate parts within from mechanical injury by hard substances +contained in the soil, serves by its comparative imperviousness to prevent +evaporation, or the escape of the sap by osmosis as it flows from the root +hairs up to the stem and leaves.</p> + +<p id="exp-44"><span class="smcap">Experiment 44. To show that roots absorb moisture.</span>—Fill two +pots with damp earth, put a healthy plant in one, and set them side by +side in the shade. After a few days examine by digging into the soil with +a fork and see in which pot it is drier. Where has the moisture gone? +How did it get out?</p> + +<p><span class="pagenum" id="Page_66">[Pg 66]</span></p> + +<p id="exp-45"><span class="smcap">Experiment 45. To show that roots shun the light.</span>—Cover the +top of a glass of water with thin netting, and lay on it sprouting mustard +or other convenient seed. Allow the roots to pass through the netting into +the water, noting the position of root and stem. Envelop the sides of +the glass in heavy wrapping paper, admitting a little ray of light through +a slit in one side, and after a few days again observe the relative position +of the two organs. How is each affected by the light?</p> + +<p id="exp-46"><span class="smcap">Experiment 46. To find out whether roots need air.</span>—Remove +a plant from a porous earthenware pot in which it has been growing for +some time; the roots will be found spread out in contact with the walls +of the pot instead of embedded in the soil at the center. Why is this?</p> + +<p id="exp-47"><span class="smcap">Experiment 47. To show that roots seek water.</span>—Stretch some +coarse netting covered with moist batting over the top of an empty tumbler. +Lay on it some seedlings, as in <a href="#exp-45">Exp. 45</a>, allowing the roots to pass through the +meshes of the netting. Keep the batting moist, but take care not to let +any of the water run into the vessel. Observe the position of the roots +at intervals, for twelve to twenty-four hours, then fill the glass with water +to within 10 millimeters (a half inch, nearly) or less of the netting, let +the batting dry, and after eight or ten hours again observe the position +of the roots. What would you infer from this experiment as to the affinity +of roots for water?</p> + +<p id="exp-48"><span class="smcap">Experiment 48. What becomes of the water absorbed by roots.</span>—Cover +a calla lily, young cornstalk, sunflower, tropæolum, or other +succulent herb with a cap of oiled paper to prevent evaporation from the +leaves, set the pot containing it in a pan of tepid water, and keep the temperature +unchanged. After a few hours look for water drops on the leaves. +Where did this water come from? How did it get up into the leaves?</p> + +<p id="exp-49"><span class="smcap">Experiment 49. To show the force of root pressure.</span>—Cut off +the stem of the plant 6 or 8 centimeters (3 or 4 inches) from the base. +Slip over the part remaining in the soil a bit of rubber tubing of about +the same diameter as the stem, and tie tightly just below the cut. Pour +in a little water to keep the stem moist, and slip in above, a short piece +of tightly fitting glass tubing. Watch the tube for several days and note +the rise of water in it. The same phenomenon may be observed in the +“bleeding” of rapidly growing, absorbent young shoots, such as grape, +sunflower, gourd, tobacco, etc., if cut off near the ground in spring when +the earth is warm and moist. By means of an arrangement like that shown +in <a href="#i_077">Fig. 81</a>, the force of the pressure exerted can be measured by the displacement +of the mercury. This flow cannot be due to the giving off of +moisture by the leaves, since they have been removed. Their action, +when present, by causing a deficiency of moisture in certain places may<span class="pagenum" id="Page_67">[Pg 67]</span> +influence the direction and rapidity of the +current, but does not furnish the motive +power, which evidently comes, in part at +least, from the roots, and is the expression +of their absorbent activity.</p> + +<figure class="figright illowp30" id="i_077" style="max-width: 21em;"> + <img class="w100" src="images/i_077.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 81.</span>—Arrangement for +estimating the force of root pressure: +<i>s</i>, stub of the cut stem; <i>g</i>, +glass tubing joined by means of +the rubber tubing, <i>t</i>, to the stem; +<i>m</i>, mercury forced up the glass +tube by water, <i>w</i>, pumped from +the soil by the roots.</p></figcaption> +</figure> + +<p id="exp-50"><span class="smcap">Experiment 50. To show that roots +cause the occurrence of acids.</span>—Lay +a piece of blue litmus paper on a board or +on a piece of glass slightly tilted at one end +to secure drainage. Cover the surface with +an inch of moist sand and plant in it a +number of healthy seedlings. Acids have +the property of changing blue litmus to +red; hence, if you find any red stains on +the paper where the roots have penetrated, +what are you to conclude?</p> + +<p>Carbon dioxide has a slight acid reaction +and is caused to form in varying +quantities by all roots. Probably other +substances, and these not a few, are actually +excreted.</p> + +<p id="exp-51"><span class="smcap">Experiment 51. Can the absorbent +power of roots be interfered with?</span>—Place +the roots of a number of seedlings +with well-developed hairs in a weak solution of saltpeter—10 grams (about +⅓ of an ounce) to a pint of water, and others in a stronger solution—say +30 grams, or 1 ounce, to a pint. Try the same experiment with weak +and strong solutions of any conveniently obtainable liquid fertilizer. +After 45 minutes or an hour examine the roots under a lens and note the +change that has taken place. What has gone out of them? What caused +the loss of the contained sap?</p> + +<p id="exp-52"><span class="smcap">Experiment 52. To test the weight of soils.</span>—Thoroughly dry +and powder a pint each of sand and clay, measure accurately, and balance +against each other in a pair of scales. Which weighs more, bulk for bulk, +a “light” soil, or a “heavy” one? (77.)</p> + +<p id="exp-53"><span class="smcap">Experiment 53. To test the capacity of soils for absorbing and +retaining moisture.</span>—Arrange, as shown in <a href="#i_078">Fig. 82</a>, a number of long-necked +bottles from which the bottom has been removed. This can be +done by making a small indentation with a file at the point desired and +leading the break round the circumference with the end of a glowing wire +or a red-hot poker. The crack will follow the heated object with sufficient<span class="pagenum" id="Page_68">[Pg 68]</span> +regularity to answer the purpose. Tie a piece of thin cloth over the mouth +of each bottle and invert with the necks extending an inch or two into +empty tumblers placed beneath. Fill all to the same height with soils of +different kinds—sand, clay, gravel, loam, vegetable mold, etc.—and pour +over each the same quantity of water from above. Watch the rate at +which the liquid filters through into the tumblers. Which loses its moisture +soonest? Which retains it longest?</p> + +<figure class="figcenter illowp75" id="i_078" style="max-width: 50em;"> + <img class="w100" src="images/i_078.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 82.</span>—Apparatus for testing the capacity of soils to take in and retain +moisture.</p></figcaption> +</figure> + +<p>Next leave the soils in the bottles dry, fill the tumblers up to the necks +of the bottles, and watch the rate at which the water rises in the different +ones. The power of soils to absorb moisture is called <em>capillarity</em>. Which +of your samples shows the highest capillarity? Which the lowest? Do +you observe any relation between the capillarity of a soil and its power of +retention?</p> +</div> + + +<p id="p-68"><b>68. Roots as holdfasts.</b>—One use of ordinary roots is +to serve as props and stays for anchoring plants to the soil. +Tall herbs and shrubs, and vegetation generally that is +exposed to much stress of weather, are apt to have large, +strong roots. Even plants of the same species will develop +systems of very different strength according as they grow +in sheltered or exposed places.</p> + +<p><span class="pagenum" id="Page_69">[Pg 69]</span></p> + +<figure class="figright illowp60" id="i_079" style="max-width: 44.75em;"> + <img class="w100" src="images/i_079.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 83.</span>—Dandelion: <i>a</i>, common form, grown in plains +region at low altitude; <i>b</i>, alpine form.</p></figcaption> +</figure> + +<p id="p-69"><b>69. Root pull.</b>—Roots are not mere passive holdfasts, +but exert an active downward pull upon the stem. Notice +the rooting end +of a strawberry or +raspberry shoot +and observe how +the stem appears +to be drawn into +the ground at the +rooting point. +In the leaf rosettes +of herbs +growing flat on +the ground or in +the crevices of walls and pavements, the strong depression +observable at the center is due to root pull. (<a href="#i_079a">Fig. 84</a>.)</p> + +<p class='cb'></p> + +<figure class="figleft illowp30" id="i_079a" style="max-width: 30.25em;"> + <img class="w100" src="images/i_079a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 84.</span>—Raspberry stolon +showing root pull.</p></figcaption> +</figure> + +<p id="p-70"><b>70. Storage of food.</b>—Another office +of roots is to store up food for the +use of the plant. This is done chiefly +in the tissues of fleshy roots and tubers, +and gives to them their great +economic value. Next to grains and +cereals, roots probably furnish a larger +portion of food to the human race +than any other crop. In addition to +this they are also the source of valuable +drugs, condiments, and dyes.</p> + +<p id="p-71"><b>71. Absorption and conveyance of +sap.</b>—But the most important function +of roots is that of absorption. +By their action the soil water and the +minerals contained in it are drawn up +into the plant body and made available +for conversion by the leaves into +organic foods, as will be explained in another chapter. From +the nature of their function, most roots have naturally a<span class="pagenum" id="Page_70">[Pg 70]</span> +strong affinity for water, and its presence or absence has a +marked influence on their direction of growth, being often +sufficient to overcome that of geotropism (<a href="#exp-47">Exp. 47</a>). There +are many trees and shrubs, notably willow, sweet bay, red +birch, and the like, that grow best on the banks of streams +and ponds, where their roots can have direct access to water. +Excess of moisture, however, is injurious to most land plants +by preventing the roots from getting sufficient air for respiration.</p> + +<p id="p-72"><b>72. The conditions of absorption.</b>—The sap in the root +cells is normally denser than the water in the soil, so there is +a continuous flow from the latter to the former. But if, +for any reason, the density of the liquids should be reversed, +the flow would set in the opposite direction, and if continued +long enough, the strength of the plant would be literally +“sapped” by the exhaustion of its tissues, so that it would +die. What is this process of cell exhaustion called?</p> + +<p id="p-73"><b>73. The use of acid secretions to the root.</b>—It was +shown in <a href="#exp-50">Exp. 50</a> that carbon dioxide and probably other substances +occur in the immediate +vicinity of roots. +Carbon dioxide is an active +agent in dissolving +the various mineral matters +contained in the soil, +and as these last can be +absorbed only in a liquid +or a gaseous state <a href="#p-63">(63)</a>, +the advantage to the +root as an absorbent organ, +of being able to secrete +such active solvents, +is obvious.</p> + +<figure class="figleft illowp40" id="i_080" style="max-width: 39.875em;"> + <img class="w100" src="images/i_080.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 85.</span>—A natural root etching, +found on a piece of slate.</p></figcaption> +</figure> + +<p id="p-74"><b>74. Relation of roots +to the soil.</b>—In order to +perform their work of absorption,<span class="pagenum" id="Page_71">[Pg 71]</span> +roots must have access to a suitable soil. To produce +the best results a soil must contain (1) all the essential +mineral constituents <a href="#p-62">(62)</a>; (2) moisture for dissolving these +materials; and (3) air enough to supply the oxygen which is +necessary to the life processes of all green plants.</p> + +<p id="p-75"><b>75. Composition of soils.</b>—Sand, clay, and humus, or +vegetable mold, with the various substances dissolved in +them, constitute the basis of cultivated soils. A mixture +of sand, clay, and humus is called loam. When the proportion +of humus is very large and well decomposed, the mixture +is called <em>muck</em>. Pure sand contains but little nourishing +matter and is too porous to retain water well. Pure clay +is too compact to be easily permeable to either air or water. +Most soils are composed of a mixture of the two with vegetable +mold in varying proportions, giving a sandy loam, or +a clay loam, as the case may be.</p> + +<p id="p-76"><b>76. Tillage.</b>—The advantages of tillage are: (<i>a</i>) that by +breaking up the hard lumps it renders the soil more permeable +to air and water and more easily penetrable by the +roots in their search for food; (<i>b</i>) the covering of loose, +friable earth left by the plow and the harrow acts as a mulch, +and by shading the soil below, prevents too rapid a loss of +water by evaporation. Where the essential food ingredients +are present, good tillage counts for more in making a crop +than the original quality of the soil.</p> + +<p id="p-77"><b>77. Light and heavy soils.</b>—These terms are used by +farmers not in relation to the weight of soils, but in reference +to the ease or difficulty with which they are worked. Light +soils contain a preponderance of sand; heavy ones, of clay.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Will plants grow better in an earthen pot or a wooden box than +in a vessel of glass or metal? Why? (<a href="#exp-46">Exp. 46</a>.)</p> + +<p>2. Which absorb more from the soil, plants with light roots and abundant +foliage, or those with heavy roots and scant foliage? (Suggestion: +roots absorb from the soil; leaves, mainly from the air.)</p> + +<p><span class="pagenum" id="Page_72">[Pg 72]</span></p> + +<p>3. Why are willows so generally selected for planting along the +borders of streams in order to protect the banks from washing? (<a href="#p-71">71</a>.)</p> + +<p>4. Why are the conducting tissues of roots at the center instead of +near the surface as in stems? (<a href="#p-67">67</a>, <i>b</i>.)</p> + +<p>5. Why does corn never grow well in swampy ground? (<a href="#p-74">74</a>; <a href="#exp-46">Exp. 46</a>.)</p> + +<p>6. Why are fleshy roots so much larger in cultivated plants than in +wild ones of the same species? (<a href="#p-74">74</a>, <a href="#p-76">76</a>.)</p> + +<p>7. When the use of a particular kind of fertilizer causes the leaves +of the plants to which it has been applied to turn brown, so that the +farmer says they have been “burned” by it, to what cause is the trouble +due? (<a href="#p-59">59</a>, <a href="#p-72">72</a>.)</p> + +<p>8. Why do farmers speak of turnips and other root crops as “heavy +feeders”? (<a href="#p-70">70</a>, <a href="#p-71">71</a>.)</p> + +<p>9. Which is more exhausting to the soil, a crop of beets, or one of oats? +Onions, or green peas? (See 2, suggestion.)</p> + +<p>10. Why will inserting the end of a wilted twig in warm water sometimes +cause it to revive? (<a href="#exp-48">Exps. 48</a>, <a href="#exp-49">49</a>.)</p> +</div> + + +<h3 id="CH_III_V">V. DIFFERENT FORMS OF ROOTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Examples of taproots: bean, pea, cotton, maple seedlings, +or any kind of very young woody root. Fibrous: any kind of grass or +grain. Fleshy: parsnip, turnip, carrot, dahlia, sweet potato. Water: +duckweed, pondweed, or a cutting of wandering Jew grown in water. +Parasitic: mistletoe, dodder, beech drops. Aërial and adventitious: the +aërial roots of old scuppernong vines, climbing roots of ivy and trumpet +vine, prop roots from the lower nodes of cornstalks and sugar cane.</p> +</div> + +<p id="p-78"><b>78. Basis of distinction.</b>—Roots vary in form and external +structure according to their origin, function, and +surroundings. In reference to the first, they are classed +as primary or secondary; in regard to the second, as dry or +fleshy; while as to surroundings, they may be adapted to +either the soil, water, air, or the parasitic habit. Soil roots +are the normal form. According to their mode of growth +they are either fibrous or axial.</p> + +<figure class="figcenter illowp51" id="i_083" style="max-width: 58.25em;"> + <img class="w100" src="images/i_083.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 3.</span>—Aërial roots of a Mexican “strangling” fig, enveloping the trunk +of a palm (<i>From</i> “Rep’t. Mo. Bot. Garden”).</p></figcaption> +</figure> + +<p id="p-79"><b>79. Taproots.</b>—These are the common form of the axial +type. Compare the root of any young hardwood cion a +year or two old with one of a mature stalk of corn or +other grain, and with the roots of seedlings of the same +species. Notice the difference in their mode of growth. In +the first kind a single stout prolongation called a taproot +proceeds from the lower end of the hypocotyl and continues +the axis of growth straight downward, unless turned aside +by some external influence. A taproot may be either simple, +as in the turnip, radish, and dandelion, +or branched, as in most shrubs and +trees. In the latter case the main axis +is called the primary root, and the +branches are secondary ones.</p> + +<p><a id="Page_73"></a><span class="pagenum" id="Page_74">[Pg 74]</span></p> + +<figure class="figleft illowp30" id="i_084" style="max-width: 22.5625em;"> + <img class="w100" src="images/i_084.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 86.</span>—Branched taproot +of maple.</p></figcaption> +</figure> + +<p id="p-80"><b>80. Fibrous and fascicled roots.</b>—Where +the main axis fails to develop, +as in the corn and grasses generally, +a number of independent branches take +its place, forming what are known as +fibrous roots. Both fibrous and taproots +may be either hard or fleshy. +The turnip and carrot are examples of +fleshy taproots, the dahlia and rhubarb of fascicled roots. +The function of both is the storage of nourishment. The +sweet potato is an example of a tuberous root.</p> + +<p id="p-81"><b>81. Practical importance of this distinction.</b>—The difference +between axial and fibrous roots has important bearings +in agriculture. The first kind, +which are characteristic of most dicotyls, +strike deep and draw their nourishment +from the lower strata of the +soil, while the fibrous and fascicled, or +radial kinds, as we may call them for +want of a better name, spread out near +the surface and are more dependent on +external conditions.</p> + +<figure class="figright illowp30" id="i_084a" style="max-width: 21.1875em;"> + <img class="w100" src="images/i_084a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 87.</span>—Fibrous root.</p></figcaption> +</figure> + +<p id="p-82"><b>82. Roots that grow above ground.</b>—The kinds of +roots that have just been considered are all subterranean, +and bring the plant into relation with the earth, whether for +the purpose of absorbing nourishment, or of mechanical support, +or, as in the majority of cases, for both. Many plants,<span class="pagenum" id="Page_75">[Pg 75]</span> +however, do not get their mineral nutrients directly from +the soil, and these give rise to various forms suited to other +conditions of alimentation.</p> + +<p id="p-83"><b>83. Adventitious roots.</b>—This name applies to any kinds +of roots that occur on stems, or in other unusual positions. +They may be considered as intermediate between the two +classes named in 81; for while their starting point is above +ground, they generally end by fixing themselves in the soil, +where they often function as normal roots. Familiar examples +are the roots that put out from the lower nodes of corn and +sugar cane stalks, and serve both to supply additional moisture +and to anchor the plant more firmly to the soil. Most +plants will develop adventitious roots if covered with earth, +or even if merely kept in contact with the ground. The +gardener takes advantage of this capacity when he propagates +by cuttings and layers.</p> + +<p id="p-84"><b>84. Water roots.</b>—These are generally white and threadlike +and more tender and succulent than ordinary soil roots, +because they have less work to do. Floating and immersed +plants, such as bladderwort and hornwort (<i>Ceratophyllum</i>) +have no need of absorbent roots, since the greater part of +their surface is in contact with water and can absorb directly +what is needed.</p> + +<p>Land plants will often develop water roots and thrive +for a time if the liquid holds in solution a sufficient quantity +of air and mineral nutrients. Place a cutting of wandering +Jew in a glass of clear water, and in from four to six days it +will develop beautiful water roots in which both hairs and +cap are clearly visible to the naked eye.</p> + +<p id="p-85"><b>85. Haustoria</b>, from a Latin word meaning to drain, +or exhaust, is a name given to the roots of parasitic plants, +or such as live by attaching themselves to some other living +organism, from which they draw their nourishment ready +made. Their roots are adapted to penetrating the substance +of the <em>host</em>, as their victim is called, and absorbing +the sap from it. Dodder and mistletoe are the best-known<span class="pagenum" id="Page_76">[Pg 76]</span> +examples of plant parasites, though the latter is only partially +parasitic, as it merely takes up the sap from the host and +manufactures its own food +by means of its green leaves.</p> + +<figure class="figright illowp30" id="i_086" style="max-width: 18.75em;"> + <img class="w100" src="images/i_086.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 88.</span>—Beech root: <i>A</i>, grown in +unsterilized wood humus: <i>p</i>, strands of +fungal hyphæ, associated at <i>a</i>, with +humus; <i>B</i>, grown in wood humus freed +from fungus by sterilization—it is not +provided with fungal hyphæ, and has +root hairs, <i>h</i>. (<i>A</i> and <i>B</i> both several +times magnified.)</p></figcaption> +</figure> + +<p id="p-86"><b>86. Saprophytes.</b>—Akin +to parasites are saprophytes, +which live on dead and decaying +vegetable matter. They +are only partially parasitic +and do not bear the haustoria +of true parasites. Many of +them, of which the Indian +pipe (<i>Monotropa</i>) and coral +root are familiar examples, +obtain their nourishment in +part, at least, by association with certain saprophytic fungi, +which enmesh their roots in a growth of threadlike fibers +that take the place of root hairs and absorb organic food +from the rich humus in +which these plants grow. +Such growths are called +<em>mycorrhiza</em>, meaning +“fungal roots.” Similar +associations are formed +by some of the higher +plants also. The rootlets +of the common beech +and of certain of the +pine family, for instance, +are often enveloped in +a network of fungus fibers, +and in this case root +hairs are developed very +poorly, or not at all. Besides greatly increasing the absorbent +surface by their ramification through the soil, the mycorrhizal +threads may possibly benefit the plant in other ways also, as,<span class="pagenum" id="Page_77">[Pg 77]</span> +for instance, by bringing +about chemical changes +that might aid in the +work of nutrition.</p> + +<figure class="figcenter illowp76" id="i_086a_2" style="max-width: 56.4375em;"> + <img class="w100" src="images/i_086a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 89.</span>—An air plant (<i>Tillandsia</i>), growing +on the underside of a bough.</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_087" style="max-width: 25em;"> + <img class="w100" src="images/i_087.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 90.</span>—A single strand of <i>Tillandsia +usneoides</i>, a rootless epiphyte belonging to the +pineapple family; better known as the “Spanish +moss” that drapes the boughs of trees so +conspicuously in the warm parts of America. +Two-thirds natural size. (Photographed by C. +F. O’Keefe.)</p></figcaption> +</figure> + +<p id="p-87"><b>87. Epiphytes, or air +plants.</b>—In the proper +meaning of the word +these are not parasitic, +but use their host merely +as a mechanical support +to bring them into better +light relations. The +name, however, is loosely +applied to all plants that +find a lodgment on the +trunks and branches of +trees, whether parasites +or true epiphytes that +draw no nourishment +from the host. Not infrequently +the latter is +killed by them through +suffocation, overweighting, +or the constriction +of the stems by close +clinging twiners.</p> + +<p id="p-88"><b>88. Aërial roots</b> are +such as have no connection +at all with the soil or +with any host plant, except +as they may lodge +upon the trunks and +branches of trees for a +support. In other than +purely epiphytic plants, +which get all their nourishment<span class="pagenum" id="Page_78">[Pg 78]</span> +from the air, they are generally subsidiary to soil +roots, like the long dangling cords that hang from some +species of old grapevines; or they subserve other purposes +altogether than absorbing nourishment, as the climbing +roots of the trumpet vine and poison ivy. A very remarkable +development of aërial roots takes place in the “strangling +fig” of Mexico and Florida, which begins life as a small +epiphyte, from seeds dropped by birds on the boughs or +trunks of trees. When it gets well started, the young plant +sends down enormous aërial roots, which find their way to +the ground, and in time so completely envelop the host that +it is literally strangled to death (<a href="#i_083">Plate 3</a>, p. 73). When this +support is removed, the sheathing roots take its place and +become to all intents +and purposes the stem +of the fig tree, which +now leads an independent +life.</p> + +<figure class="figright illowp40" id="i_088" style="max-width: 39.6875em;"> + <img class="w100" src="images/i_088.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 91.</span>—Root system of a tobacco plant.</p></figcaption> +</figure> + +<p id="p-89"><b>89. The root system.</b>—The +entire mass of +roots belonging to a +plant, with all its ramifications +and subdivisions, composes a root +system. The extent of root expansion is in general about +equal to that of the crown, thus bringing the new and +active parts under the drip of the boughs where the moisture +is most abundant. Some plants have root systems out of +all seeming proportion to their size. A catalpa seedling +six months old showed, by actual measurement, 250 feet +of root growth, and it is estimated that the roots of a thrifty +cornstalk, if laid end to end, would extend a mile. In the +development of the root system, a great deal depends upon +external conditions. In a poor, dry soil, the roots have to +travel farther in search of a livelihood, and so a larger system +has to be developed than in a more favorable location.</p> + +<p><span class="pagenum" id="Page_79">[Pg 79]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Which is better to succeed a crop of turnips on the same land, hay +or carrots? (<a href="#p-81">81</a>.)</p> + +<p>2. Write out what you think would be a good rotation for four or +five successive crops based on the forms of the roots.</p> + +<p>3. Study the following rotations and give your opinion about them, +on the same principle. Suggest any improvements that may occur to +you, and give a reason for the change. Beets, barley, clover, wheat; +cotton, oats, peas, corn; oats, melons, turnips; cotton, oats, corn and +peas mixed, melons; cotton, hay, corn, peas.</p> + +<p>4. Give three good reasons in favor of a rotation over a single-crop +system. (<a href="#p-24">24</a>, <a href="#p-60">60</a>, <a href="#p-62">62</a>, <a href="#p-81">81</a>.)</p> + +<p>5. Which will require deeper tillage, a bed of carrots or one of strawberries? +(<a href="#p-81">81</a>.)</p> + +<p>6. Explain why some plants keep green and fresh when the surface +of the soil is dry, while others wilt or die. (<a href="#p-81">81</a>, <a href="#p-89">89</a>.)</p> + +<p>7. Which will better withstand drought, a crop of alfalfa or one of +Indian corn? Why? (<a href="#p-81">81</a>.)</p> + +<p>8. Which will interfere less with the trees if planted in an orchard, +beets or onions? (<a href="#p-81">81</a>.)</p> + +<p>9. Ought a crop of hemp and tobacco to succeed each other on the +same land? (<a href="#p-81">81</a>, <a href="#p-89">89</a>.)</p> + +<p>10. Why does a gardener manure a grass plot by scattering the fertilizer +on the surface, while he digs around the roses and lilacs and deposits +it under ground? (<a href="#p-81">81</a>.)</p> + +<p>11. Do the adventitious roots of such climbers as ivy and trumpet vine +draw any nourishment from the objects to which they cling? (<a href="#p-83">83-88</a>.)</p> + +<p>12. How can you tell?</p> + +<p>13. Do partial dependents of this kind injure trees by climbing upon +them; and if so, how? (<a href="#p-87">87</a>, <a href="#p-88">88</a>.)</p> + +<p>14. What is the use of the aërial roots of the scuppernong grape? (<a href="#p-88">88</a>.)</p> + +<p>15. Is the resurrection fern (<i>Polypodium incanum</i>), that grows on tree +trunks in our Southern States, a parasite or an air plant? (<a href="#p-87">87</a>.)</p> + +<p>16. On what plants in your neighborhood does mistletoe grow most +abundantly? Dodder?</p> + +<p>17. Is mistletoe injurious to the host? (<a href="#p-85">85</a>.)</p> + +<p>18. Name some plants that are propagated mainly, or solely, by roots +and cuttings.</p> + +<p>19. Where do aërial roots get their nourishment? (<a href="#p-88">88</a>.)</p> + +<p>20. Would they be of any use to a plant in a very cold or dry climate?</p> + +<p>21. Where should manure be placed to benefit a tree or shrub with +wide-spreading roots? (<a href="#p-66">66</a>, <a href="#p-89">89</a>.)</p> + +<p><span class="pagenum" id="Page_80">[Pg 80]</span></p> + +<p>22. Is it a wise practice to mulch a tree by raking up dead leaves and +piling them around the base of the trunk, as is often done? Why, or why +not? (<a href="#p-66">66</a>, <a href="#p-89">89</a>.)</p> +</div> + + +<h4 id="CH_III_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>(1) Examine the underground parts of hardy winter herbs in your neighborhood, +also of any weeds or grasses that are particularly troublesome, +and see if there is anything about the structure of these parts to account +for their persistence. Note the difference between roots of the same species +in low, moist places and in dry ones; between those of the same kind of +plants in different soils; in sheltered and in exposed situations. Study +the direction and position of the roots of trees and shrubs with reference +to any stream or body of water in the neighborhood. (The elm, fig, +mulberry, and willow are good subjects for such observations.) Notice +also whether there is any relation between the underground parts and the +leaf systems of plants in reference to drainage and transpiration.</p> + +<p>(2) Observe the effect of root pull upon low herbs. Look along washes +and gullies for roots doing the office of stems, and note any changes of +structure consequent thereon. Study the relative length and strength +of the root systems of different plants, with reference to their value as +soil binders, or their hurtfulness in damaging the walls of cellars, wells, +sewers, etc. Dig your trowel a few inches into the soil of any grove +or copse you happen to visit, note the inextricable tangle of roots, and +consider the fierce competition for living room in the vegetable world that +it implies.</p> + +<p>(3) Tests might be made of the different soils in the neighborhood of +the schoolhouse by planting seeds of various kinds and noting the rate of +germination; first, without fertilizers, then by adding the different elements +in succession to see what is lacking. The field for study suggested +by this subject is almost inexhaustible.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_81">[Pg 81]</span></p> + +<h2 class="nobreak" id="CH_IV">CHAPTER IV. THE STEM</h2> +</div> + + +<h3 id="CH_IV_I">I. FORMS AND GROWTH OF STEMS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Vigorous young hop or beau seedlings grown in pots; +a fresh dandelion stalk; a stem of pea, squash, cucumber, grape, or passion +flower vine, with tendrils.</p> + +<p><span class="smcap">Appliances.</span>—A bowl of fresh water; rods of different sizes and +smoothness for testing the hold of climbers.</p> + +<p id="exp-54"><span class="smcap">Experiment 54. To show the movements of twining stems.</span>—Raise +a young hop or bean seedling in the schoolroom and allow it to grow +about two decimeters—8 to 10 inches—in length before providing it +with a support. Does the stem form any coils? Bring it in contact +with a suitable upright support and watch for a day or two. What +happens? Notice whether it starts to coil from right to left or from left +to right and see if you can coax it to turn in the opposite direction. When +it has reached the end of its stake, allow it to grow about five centimeters +(two inches, approximately) beyond, and watch the revolution of the tip. +Cut a hole through the center of a piece of cardboard about 14 centimeters +(five to six inches) in diameter, slip it over the loose end of the stem, +and fasten it to the stake in a horizontal position, with a pin. Note the +position of the stem tip at regular intervals and mark on the cardboard; +how long does it take to complete a revolution? Does it continue to coil, +or to coil as readily, after leaving its stake as before? What would you +infer from this as to the effect of contact in stimulating it to coil?</p> + +<p>Find out by experiment if it can climb well by means of a glass or other +smooth rod; by a fine wire; a broomstick; a large, smooth post. See +whether it does better on a horizontal or an upright support.</p> + +<p id="exp-55"><span class="smcap">Experiment 55. To illustrate the coiling of stems.</span>—Run a +gathering thread in one side of a narrow strip of muslin and notice how +the ruffle thus drawn will curl into a spiral when allowed to dangle from +the needle. Can you think of any cause that might act on a stem in the +same way? Suppose, for instance, that one side should grow faster than +the other; what would be the effect? (54.)</p> + +<p>Split the stem of a fresh dandelion, or other herbaceous scape, longitudinally, +and immerse it in a pan of fresh water for a few minutes. Notice +how the two halves curve outward, or even coil up like the strip of muslin. +This is due to the tension caused by the more rapid absorption of the<span class="pagenum" id="Page_82">[Pg 82]</span> +thinner walled cells of the internal tissues. These, when relieved of the +resistance of the thicker walled outer tissues, swell on their free side, but +are held back on the other by the non-absorbent outer parts, as one side +of the muslin ruffle was held by the gathering thread.</p> + +<p id="exp-56"><span class="smcap">Experiment 56. To find out whether the direction of stem +growth is influenced by light.</span>—Place two rapidly growing young +pea, bean, sunflower, or squash plants, each with several well-developed +leaves, in a room or box with a light exposure on one side only. After two +or three days, notice the position of the stems in regard to the light. Does +either one show a more decided inclination toward it than the other?</p> + +<p id="exp-57"><span class="smcap">Experiment 57. Is the light relation of the stem influenced +by the leaves?</span>—Cut the leaves from one of the plants used in <a href="#exp-56">Exp. 56</a>, +covering the cut surfaces with vaseline to prevent “bleeding”; reverse +the positions of both with regard to the light, and watch for two or three +days. In which is the response to light the more rapid? What does this +indicate as one object of the stem in seeking light? What is the best +position of a stem, ordinarily, for getting its leaves into the light?</p> +</div> + +<figure class="figright illowp40" id="i_092" style="max-width: 39.6875em;"> + <img class="w100" src="images/i_092.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 92.</span>—Stems of red oak and hickory that +have grafted themselves.</p></figcaption> +</figure> + +<p id="p-90"><b>90. Classification.</b>—Stems are classed according to +(1) duration, as annuals, biennials, and perennials; (2) with +reference to hardness or +softness of structure, as +herbaceous and woody; +(3) in regard to position +and direction of growth, +as erect, prostrate, climbing, +inclined, declined, +underground, etc.</p> + +<p id="p-91"><b>91. Annuals</b> complete +their life cycle in a +single season and then +die down as soon as they +have perfected their +seed. Many of our most +troublesome weeds belong +to this class and +might be exterminated by the simple expedient of mowing +them down before their time of flowering.</p> + +<p><span class="pagenum" id="Page_83">[Pg 83]</span></p> + +<p id="p-92"><b>92. Biennials</b>, as the name implies, live for two years. +Their energy during the first season is spent chiefly in laying +by a store of nourishment, +usually in the tissues of +fleshy roots <a href="#p-70">(70)</a>. By this +means they get a good start +in the second season and +mature their seeds early. +Many of our common garden +vegetables, such as turnips, +carrots, parsnips, and +cabbage, belong to this +class. Where is the nourishment +stored in the cabbage?</p> + +<figure class="figright illowp40" id="i_093" style="max-width: 39.25em;"> + <img class="w100" src="images/i_093.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 93.</span>—A biennial plant, mullein, in +winter condition with stem reduced to +little more than a disk supporting a rosette +of leaves. Notice how close they cling to +the earth, and compare them with their +fruiting condition a few months later as +shown in <a href="#i_191a">Fig. 237</a>.</p></figcaption> +</figure> + +<p id="p-93"><b>93. Perennials</b> are plants +that live on indefinitely, like +most of our forest trees +and woody-stemmed shrubs. +Woody stems are usually perennial and may live for hundreds +and even thousands of years, as those of the giant +sequoias of California, and the famous chestnut of Mt. +Etna.</p> + +<p id="p-94"><b>94. Herbaceous stems</b> are more or less succulent and die +down after fruiting. They are usually annuals, though some +kinds, like the garden geraniums and the common St.-John’s-wort, +show a tendency to become woody, especially at the +base, and live on from year to year. Others, such as the +hawkweed and dahlia, die down above ground in winter, +but are enabled to keep their underground parts alive indefinitely, +through the nourishment stored in them, and are +thus perennial below ground and annual above. Woody-stemmed +annuals, such as the cotton and castor oil plant, +are not, properly speaking, herbs. In the tropical countries +to which they belong they are perennial shrubs, or even +small trees, but on being transplanted to colder regions<span class="pagenum" id="Page_84">[Pg 84]</span> +have been compelled to take on the annual habit as an +adaptation to climate.</p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp90" id="fig94" style="max-width: 31.25em;"> + <img class="w100" src="images/i_094_94.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 94.</span>—Orange hawkweed with runners.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp90" id="fig95" style="max-width: 56.75em;"> + <img class="w100" src="images/i_094_95.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 95.</span>—Prostrate stem of Lycopodium with assurgent branches.</p> + </figcaption> +</figure></td></tr></table> + +<figure class="figright illowp20" id="i_094" style="max-width: 25em;"> + <img class="w100" src="images/i_094.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 96.</span>—Diagram +of stem growth: <i>ps</i>, +surface of the ground; +<i>e</i>, erect position; <i>d</i>, +declined; <i>a</i>, assurgent; +<i>p</i>, prostrate; <i>u</i>, vertical +direction underground.</p></figcaption> +</figure> + +<p id="p-95"><b>95. Direction and habit of growth.</b>—As to manner of +growth, there are many forms, from the upright boles of +the beech and pine to the trailing, prostrate, and creeping +stems of which we have examples in the +running periwinkle, the prostrate spurge +and the creeping partridge berry (<i>Mitchella +repens</i>), respectively. Trailing and prostrate +stems are very apt to become +creepers by the development of adventitious +roots at their nodes wherever they +come in contact with the soil. The rooting +stems of dewberries, the runners and +stolons of strawberries and currants, are +familiar examples.</p> + +<p>Between the extremes of prostrate and +upright, stems may be inclined or bent in +various degrees. As shown in <a href="#i_094">Fig. 96</a>, +there are two modes of inclination: <em>assurgent</em>, +<i>a</i>, from the prostrate, <i>p</i>, toward the +upright, <i>e</i>; and <em>declined</em>, <i>d</i>, from the upright<span class="pagenum" id="Page_85">[Pg 85]</span> +toward the prostrate. Below the surface, <i>ps</i>, occur only +underground stems. Is the prostrate habit an advantageous +one for light exposure? Can you think of any compensating +advantages a plant might derive from it; for example, +in regard to warmth and moisture?</p> + +<figure class="figright illowp40" id="i_095" style="max-width: 26em;"> + <img class="w100" src="images/i_095.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 97.</span>—Twining stems: +<i>A</i>, hop twining with the sun; +<i>B</i>, convolvulus twining against +the sun.</p></figcaption> +</figure> + +<p id="p-96"><b>96. Climbing stems.</b>—These are such as lift themselves +from the ground and attain the advantages of the upright +position by clinging to supports of +various kinds—usually, in a state +of nature, the stems and boughs of +other plants. The means of climbing +may be: (1) by merely leaning +upon or propping themselves up by +the aid of the supporting object—examples, +the rose, wistaria, star jessamine +(<i>Jasminum officinalis</i>); (2) by +coiling their main axes spirally +around the support—hop, bean, +morning-glory; (3) by means of adventitious +roots—poison ivy, common +English ivy, trumpet vine +(<i>Tecoma radicans</i>); (4) by organs specially developed for +the purpose, called tendrils—gourd, cucumber, grape, passion +flower.</p> + +<figure class="figright illowp40" id="i_096" style="max-width: 29.375em;"> + <img class="w100" src="images/i_096.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 98.</span>—Leaf of common pea, +showing upper leaflets reduced to +tendrils.</p></figcaption> +</figure> + +<p id="p-97"><b>97. Tendrils.</b>—The part assigned to do the work of climbing +may be a secondary branch, a flower stem, a leafstalk, a +leaf, a leaflet, or a group of leaflets (<a href="#i_096">Fig. 98</a>). Tendrils behave +in general very much like twining stems, except that they +are more sensitive and respond more quickly to any cause +that may influence their movement. While young, their +tips revolve just as do the tips of twining stems, until they +meet with an object round which they can coil. When this +happens, not only the part in contact with the object coils, +but the free part between it and the main axis will usually +respond by twisting itself into a helix (<a href="#i_096a">Fig. 99</a>). As the +distance between the base and tip of the tendril is shortened<span class="pagenum" id="Page_86">[Pg 86]</span> +by coiling, the body of the plant +is drawn upward proportionally. +It will be observed that the helix +is interrupted at one or more +points, above and below which +the coils turn in opposite directions. +This is because the tendril +is attached at both ends and +cannot adjust itself to the opposite +strains of torsion. Twist +with your fingers a piece of tape +so attached, and you will see +that on one side of your hand it +turns from right to left and on +the other from left to right.</p> + +<p id="p-98"><b>98. The cause of twining.</b>—Botanists +are not fully agreed +on this point. The explanation +most generally accepted at present is that the twining of +stems is due to the combined action of lateral and negative +geotropism <a href="#p-51">(51)</a>. The first +causes one side to grow +more rapidly than the other, +thus forming a succession of coils, while the +second, by stimulating the upward growth +of the axis, stretches it into a spiral, and in +this way draws it more tightly round the +support. For this reason twining stems do +best on an upright support.</p> + +<figure class="figcenter illowp77" id="i_096a" style="max-width: 54.0625em;"> + <img class="w100" src="images/i_096a.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Fig. 99.</span>—Stems +of a passion flower transformed into +tendrils. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p>In tendrils, the twining is thought to be +due not to gravity, but to contact with a +solid body, which, by inducing unequal development +on opposite sides of the tendril, +causes it to turn about an available object. +The coiling of the free part of the twining +organ is in response to the stimulus transmitted<span class="pagenum" id="Page_87">[Pg 87]</span> +from the part in contact—<em>stimulus</em>, in this sense, +denoting the influence of any external agent that calls forth +a responsive adjustment on the part of the plant.</p> + +<figure class="figright illowp40" id="i_097" style="max-width: 38.75em;"> + <img class="w100" src="images/i_097.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 100.</span>—Showing the economy of +labor and building material effected by the +climbing habit. Notice how the grapevine +coils like an anaconda around the tree +boles, and overtops their tallest branches. +Compare the diameter of the vine with that +of the trees.</p></figcaption> +</figure> + +<p id="p-99"><b>99. The object of the +various habits of stem +growth.</b>—To bring the +growing parts of the plant +into the best possible relations +with light and air is +one of the special functions +of the stem, and the +various habits of growth +described in this section +have been developed with +reference to this function. +In the case of prostrate +and underground stems +other factors may intervene; +can you name some of the +causes that might influence +the position of the stem in +such cases?</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why is the normal direction of most stems upright? (<a href="#exp-56">Exp. 56</a>.)</p> + +<p>2. Name a dozen woody-stemmed plants; a dozen with herbaceous +stems.</p> + +<p>3. Name all the plants you can think of that have prostrate stems, or +leaf rosettes that hug the earth, like mullein and dandelion. Which of +these are wintergreen plants? Which are hot-weather growers?</p> + +<p>4. Can you explain in what ways both hot-weather and cold-weather +plants may be advantaged by the habit of clinging close to the earth? +(<a href="#p-94">94</a>, <a href="#p-95">95</a>.)</p> + +<p>5. Is there any difference in the height of the stem of a dandelion flower +and a dandelion ball?</p> + +<p>6. Of what advantage is this to the plant? (<a href="#exp-17">Exp. 17</a>.)</p> + +<p>7. Name all the means you can think of by which a stem may climb, +and give an example of each.</p> + +<p><span class="pagenum" id="Page_88">[Pg 88]</span></p> + +<p>8. Why do we support peas with brush, and hops or beans with poles? +(<a href="#p-98">98</a>; <a href="#exp-54">Exp. 54</a>.)</p> + +<p>9. Are the vines of gourds, watermelons, squashes, and pumpkins +normally climbing or prostrate? How can you tell? (<a href="#p-96">96</a>, <a href="#p-97">97</a>.)</p> + +<p>10. Why does not the gardener provide them with poles or trellises to +climb on?</p> + +<p>11. Do twining plants grow equally well on horizontal and upright +supports? (<a href="#p-98">98</a>; <a href="#exp-54">Exp. 54</a>.)</p> + +<p>12. If there is any difference, which do they seem to prefer?</p> + +<p>13. Can you give any reasons for thinking that the climbing habit +might lead to parasitism? (<a href="#p-83">83</a>, <a href="#p-85">85</a>, <a href="#p-87">87</a>.)</p> + +<p>14. What method of climbing would be most favorable to the development +of such a habit? (Suggestion: What mode of climbing brings the +stem into closest contact with its support?)</p> + +<p>15. Name some plants the stems of which are used as food.</p> + +<p>16. Name some from which gums and medicines are obtained.</p> + +<p>17. Explain how it can benefit a plant to have its leaves, or some of +them, modified into tendrils. (<a href="#p-99">99</a>.)</p> + +<p>18. In what way is the loss of the normal function of the leaves so modified, +compensated for? (<a href="#exp-57">Exp. 57</a>.)</p> + +<p>19. Suppose the vine shown in <a href="#i_097">Fig. 100</a> had to lift itself without the aid +of a support; could it reach the same height and carry the same weight +of foliage and flowers with the same expenditure of labor and building +material?</p> +</div> + + +<h3 id="CH_IV_II">II. MODIFICATIONS OF THE STEM</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A shoot of asparagus; thorny branches of locust, plum, +or haw; a cactus plant; bulbs of lily and hyacinth or onion; tubers of +potato; rootstocks of iris, fern, or violet. If fresh specimens are not accessible, +dried rootstocks of the sweet flag and Florentine iris may be obtained +at the drug stores under the names of calamus and “orris” root.</p> +</div> + +<p id="p-100"><b>100. How to recognize modified parts.</b>—Stems, like +roots, are often modified to serve other than their normal +purpose, and in adapting themselves to these new functions +they sometimes undergo such changes of form and structure +that it would be impossible to recognize their true nature +from appearances alone. The safest tests in such cases +are: (1) by a comparison of the parts of the modified structure +with those of known organs of the same kind; and (2) by +observing its position in reference to other parts. For<span class="pagenum" id="Page_89">[Pg 89]</span> +instance, we know that the stem is the part of the plant which +normally bears leaves and flowers, and if either of these, +or if the small scales which often take the place of leaves, +are found growing on any plant structure, we may usually +take for granted that it is a stem. Then, again, as will be +shown in the next chapter, buds and branches naturally +appear only at the nodes, in or near the <i>axil</i>, or inner angle +made by a leaf with the stem. Hence, if you see any growth +springing from such a position, you may generally conclude +it to be a stem.</p> + +<figure class="figright illowp30" id="i_099" style="max-width: 26.5em;"> + <img class="w100" src="images/i_099.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 101.</span>—Stem-leaves +(cladophylls) of a ruscus, bearing +flowers.</p></figcaption> +</figure> + +<p id="p-101"><b>101. Stems as foliage.</b>—The connection between stem +and leaf is so intimate that we need not be surprised to find +a frequent interchange of function +between them, the leaf, or some part +of it, doing the work of the stem +(<a href="#i_096">Fig. 98</a>), the stem more often taking +upon itself the office of the leaf. A +common example is the garden asparagus. +Examine one of the young +shoots sold in the market, and notice +that it bears a number of small scales +in place of leaves. On an older +shoot that has gone to seed, the +green, threadlike appendages, which +are usually taken for foliage, will be +found to spring each from the axil +of one of these scales. What, therefore, are we to conclude +that it is?</p> + +<p>In the butcher’s-broom of Europe, the transformation has +gone so far that the branches of the stem have assumed the +flattened appearance of leaves (<a href="#i_099">Fig. 101</a>), but their real +nature is evident both from their position in the axils of +leaf scales, and from the fact that they bear flower clusters +in the axil of a scale on their upper face. Another example +of this sort of modification is seen in the pretty little <i>myrsiphyllum</i> +of the greenhouses (wrongly called smilax), which<span class="pagenum" id="Page_90">[Pg 90]</span> +is so much used for decoration. +The delicate green blades are +merely altered stems, shortened +and flattened to simulate leaves.</p> + +<figure class="figleft illowp30" id="i_100" style="max-width: 29.0625em;"> + <img class="w100" src="images/i_100.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 102.</span>—Thorn branches of +<i>Holocantha Emoryi</i>, a plant growing +in arid regions.</p></figcaption> +</figure> + +<p id="p-102"><b>102. Weapons of defense.</b>—Conspicuous +examples of these +are the bristling thorns of the +honey locust. Is their frequent +branching any indication of their +real nature? Does it <em>prove</em> anything, +or must you look for other +evidence? What further indications +might you expect to +find, if they are true branching +stems? <a href="#p-100">(100.)</a> On old haw, +plum, crab, and pear trees, stems can be found in all stages +of transition, from stubby, ill-developed branches, to well-defined +thorns.</p> + +<figure class="figright illowp25" id="i_100a" style="max-width: 14.3125em;"> + <img class="w100" src="images/i_100a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 103.</span>—Melon +cactus, showing +greatly condensed +stem for the storage +and preservation of +moisture.</p></figcaption> +</figure> + +<p id="p-103"><b>103. Storage of nourishment.</b>—This is +one of the most frequent causes of modification +in both roots and stems. Of stems +that grow above ground, the sugar cane +probably comes first in economic importance +on this account. In hot, arid regions, where +the moisture drawn from the earth would, +during prolonged drought, be too rapidly +dissipated by an expanded surface of leaves, +the whole plant, as in the case of the cactus, +is sometimes compacted into a greatly thickened +stem, which fills the triple office of leaf, +stalk, and water reservoir.</p> + +<figure class="figright illowp25" id="i_101" style="max-width: 15.25em;"> + <img class="w100" src="images/i_101.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 104.</span>—Rootstock +of creeping +panic grass.</p></figcaption> +</figure> + + +<p id="p-104"><b>104. The uses of underground stems.</b>—It +is in these that the storage of nourishment +most frequently takes place, and the modifications +that stems undergo for this purpose +are in some cases so great that their real<span class="pagenum" id="Page_91">[Pg 91]</span> +nature becomes apparent only after a careful examination. +But while the chief function of underground stems is the +storage of nourishment, they serve other purposes also. In +plants requiring a great deal of moisture, +like the ferns, and in others growing in dry +places and needing to husband moisture +carefully, like the blackberry lily, underground +stems may be useful in preventing +the too rapid evaporation that would take +place through aërial stems. Defense against +frost, cold, heat, and other dangers, as well +as quickness of propagation, are also attained +or assisted by this means.</p> + +<p id="p-105"><b>105. Rootstocks and rhizomes.</b>—From a +prostrate stem like that shown in <a href="#fig95">Fig. 95</a> to a +creeping rootstock like the one in <a href="#i_101">Fig. 104</a>, the +transition is so easy that we find no difficulty +in accounting for it. From the prostrate rootstock to the +thickened storage rhizome (<a href="#i_101a">Fig. 105</a>) of such plants as the iris, +puccoon, bulrush, and Solomon’s-seal, is a longer step, but +the bud with its leaf scales at the growing tip, <i>a</i>, the remains +of the flower stem at the node, <i>b</i>, and the roots from the under +surface sufficiently indicate its nature. +The peculiar scars from which +the Solomon’s-seal takes its name +are caused by the falling away +each year of the flowering stem +of the season after its work is done, +leaving behind the node of the underground +stem from which it originated. +In this way the rhizome lives on indefinitely, +growing and increasing at one end as fast as it dies at +the other. Test a little of the substance of the rhizome +with iodine. Of what does it consist? Of what use is it +to the plant?</p> + +<figure class="figcenter illowp100" id="i_101a" style="max-width: 15.0em;"> + <img class="w100" src="images/i_101a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 105.</span>—Rhizome of Solomon’s-seal: +<i>a</i>, growing bud at the tip; <i>b</i>, remains of the past +season’s flower stem; <i>c</i>, <i>c</i>, <i>c</i>, scars +of old stems. (<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_102" style="max-width: 33.5em;"> + <img class="w100" src="images/i_102.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 106.</span>—Potato tuber showing lenticels, +<i>A</i>, <i>A</i>, or pores for air on the surface; +<i>S</i>, leaf scale, or scar.</p></figcaption> +</figure> + +<p id="p-106"><b>106. The tuber.</b>—A still further thickening and shortening<span class="pagenum" id="Page_92">[Pg 92]</span> +of the rhizome gives rise to the tuber, of which the +potato and the Jerusalem artichoke are familiar examples. +Can you give any evidence to show that the potato is a +modified stem? Find the +point of attachment of the +tuber to its stem and stand +it on this end, which is its +natural base. Notice that +the eye sits in the axil of +the little scale that forms +the eyelid. What does the +scale represent? What is +the eye? <a href="#p-100">(100.)</a> Do the +scales occur in any regular +order—that is, opposite, or alternating with, each other, like +the leaves on a stem? Look on the surface for a number of +small, lens-shaped dots (<i>A</i>, <i>A</i>, <a href="#i_102">Fig. 106</a>) scattered irregularly +over it. These are aërating pores called <i>lenticels</i>, and are +found in most dicotyl +stems. Does their +presence help to throw +light on the real nature +of the tuber? If any +sprouts occur on your +specimen, where do +they originate? Where +do buds and sprouts +originate on plants +above ground? Make +a sketch of the outside +of a potato, showing +the lenticels, eyes, and +scales, or the scars left +by the scales in case they have fallen away, as has probably +happened, if your specimen is an old one.</p> + +<figure class="figright illowp40" id="i_102x" style="max-width: 30em;"> + <img class="w100" src="images/i_102x.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 107, 108.</span>—Transverse +and longitudinal +sections of the +potato: <i>A</i>, skin; <i>B</i>, +cortical layer; <i>C</i>, outer +pith layer; <i>D</i>, inner pith +layer.</p></figcaption> +</figure> + +<p>Cut a small slice from the stem end of two potatoes, stand<span class="pagenum" id="Page_93">[Pg 93]</span> +them in coloring fluid for four or five hours, then divide into +cross and vertical sections, as shown in <a href="#i_102x">Figs. 107, 108</a>, and +draw, labeling the parts that you can make out. Through +which has the liquid ascended most rapidly? Test with +iodine and find out in which part nourishment is most abundant. +It is this abundant store of food that makes the +potato such a valuable crop in cold countries like Norway +and Iceland, where the seasons are too short to admit of the +slow process of developing the plant from the seed.</p> + +<figure class="figright illowp40" id="i_103x" style="max-width: 30em;"> + <img class="w100" src="images/i_103x.jpg" alt=""> + <figcaption> +<table class="autotable"> +<tr> +<td class="tdl wd50 vat"><p><span class="smcap">Fig.</span> 109.—Scaly bud of oak, enlarged.</p></td> +<td class="tdl vat"><p><span class="smcap">Fig.</span> 110.—Scaly bulb of lily (<span class="smcap">Gray</span>).</p></td> +</tr> +</table> +</figcaption> +</figure> + +<p>Compare a common potato with a sweet potato. Are +there any eyes or buds on the latter? Is there a scale below +them? Do they occur in any regular order? Do you see +any lenticels? The common potato and the sweet potato +are both tubers; can you give some of the reasons why the +one is regarded as a modified +branch, and the other +as a root? <a href="#p-100">(100.)</a> Compare +their food contents; +which contains most +starch? Which most +sugar? How can you +judge about the sugar without +a chemical test?</p> + +<p id="p-107"><b>107. The bulb</b> is a form of underground stem reduced to a +single bud. Get the scaly bulb of a lily, and sketch it from +the outside and in cross and vertical section. Compare it +with the scaly winter buds of the oak and hickory, or other +common deciduous tree. Make an enlarged sketch of the +latter on the same scale as the lily bulb, and the resemblance +will at once become apparent. The scales of the bulb are, in +fact, only thick, fleshy leaves closely packed around a short +axis that has become dilated into a flat disk. From the center +of the disk, which is the terminal node of this transformed +stem, rises the flower stalk, or <em>scape</em>, as it is called, of the +season. After blossoming, the scape perishes with its bulb, +and their place is taken by new ones which are developed<span class="pagenum" id="Page_94">[Pg 94]</span> +from the axils of the scales, thus revealing their leaflike +nature.</p> + +<figure class="figright illowp20" id="i_104" style="max-width: 12.5em;"> + <img class="w100" src="images/i_104.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 111.</span>—Leaf +of an onion divided +lengthwise showing +the base enlarged +into the coat of a +bulb.</p></figcaption> +</figure> + +<p>That bulbs are only modified buds is further shown by +the bulblets that sometimes appear among the flowers of the +onion, and in the leaf axils of certain lilies. +They never develop into branches, but drop +off and grow into new plants just as the +subterranean bulbs do.</p> + +<p>The bulbs of the onion and hyacinth are +still further modifications, in which the scales +consist of the thickened bases of leafstalks +that are dilated until each one completely +envelops the growing parts within.</p> + +<p id="p-108"><b>108. Morphology</b> is the part of botany +that treats of the origin, form, and uses +of the different organs of plants, and of +the modifications they undergo in adapting themselves to +changes of condition or function. Organs or parts that +have the same origin but have become adapted to different +functions, like the flattened stems of the butcher’s-broom +or the bulb scales of the lily, are said to be +<em>homologous</em>; those that are different in origin but adapted +to the same function, as the sweet and common potatoes, +are <em>analogous</em>. In other words, homologous organs +are morphologically alike, but may be physiologically different; +analogous organs are alike physiologically, but +differ morphologically.</p> + +<p id="p-109"><b>109. Economic value of stems.</b>—We probably get a +greater variety of economic products from the stem than +from any other part of the plant. Consider the vast +amount of food stored in underground stems like the potato; +the resins, gums, and sugar found in the sap of plants +like the sugar cane, the pine, and India-rubber trees; the +medicines, dyes, and extracts obtained from the tissues; the +valuable fibers, such as flax, jute, and hemp, furnished by +the bast; the wood pulp for making paper; and the timber<span class="pagenum" id="Page_95">[Pg 95]</span> +for building and furnishing our houses that we get from the +woody trunks of trees. When we think of all these things, +it seems hardly possible to overestimate the importance of +this part of the vegetable kingdom to man, or to exert +ourselves too strenuously to regulate and prevent the destruction +of these invaluable natural resources.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Would you judge from the observations made in the foregoing section, +that the work of an organ determines its form, or that the form determines +its work? (<a href="#p-99">99</a>, <a href="#p-100">100</a>, <a href="#p-108">108</a>.)</p> + +<p>2. Which is the more important, form or function?</p> + +<p>3. Name some plants that are propagated by rootstocks; by runners +or stolons; by rhizomes; by tubers; by bulbs.</p> + +<p>4. What is the advantage of propagating in this way over planting the +seed? (<a href="#p-104">104</a>, <a href="#p-106">106</a>.)</p> + +<p>5. Mention any other advantages that the various plants named may +gain from the development of their underground parts. <a href="#p-104">(104.)</a></p> + +<p>6. What makes the nut grass so troublesome to farmers in some parts +of the country?</p> + +<p>7. Is its “nut” a root or a tuber? How can you tell? <a href="#p-106">(106.)</a></p> + +<p>8. Suggest some ways for destroying weeds that are propagated in this +way.</p> + +<p>9. Could you get rid of wild onions in a pasture by mowing them down? +By digging them up? <a href="#p-107">(107.)</a></p> + +<p>10. Is it wise for farmers to neglect the appearance of such a weed +in their neighborhood, even though it does not infest their own land?</p> + +<p>11. Name any plants of your neighborhood, either wild or cultivated, +that are valued for their rhizomes; for their tubers.</p> + +<p>12. What part of the plants named below do we use for food or other +purposes? Ginger, angelica, ginseng, cassava, arrowroot, garlic, onion, +sweet flag, iris, sweet potato, Cuba yam, artichoke.</p> + +<p>13. Why are the true roots of bulbous and rhizome-bearing plants +generally so much smaller in proportion to the other parts than those of +ordinary plants? (<a href="#p-89">89</a>, <a href="#p-104">104</a>.)</p> + +<p>14. If the Canada thistle grows in your vicinity, examine the roots and +see if there is anything about them that will help to account for its hardihood +and persistency.</p> + +<p>15. If you live in the region of the horse nettle (<i>Solanum Carolinense</i>), +explain how it is helped by its root system. (<a href="#p-89">89</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_96">[Pg 96]</span></p> + + +<h3 id="CH_IV_III">III. STEM STRUCTURE</h3> + + +<h4 id="CH_IV_III_A">A. <span class="smcap">Monocotyls</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Fresh cornstalks with several well-developed nodes, +some of which should have stood in coloring fluid from 1 to 3 hours. If +fresh specimens cannot be obtained from the fields, a number of seedlings +may be grown in boxes of rich earth and cared for by the pupils either at +home or in the schoolroom; they should be planted 4 or 5 weeks before +needed. Asparagus and smilax sprouts may be used, or the stem of any +large grass, or of wheat and other grains, but stalks of corn or sugar cane +make the best subjects for study where they can be obtained.</p> + +<p><span class="smcap">Appliances.</span>—A compound microscope will be needed for detailed +study. Prepared slides can be used, but it is better for students to make +their own sections where practicable.</p> +</div> + +<figure class="figright illowp25" id="i_106" style="max-width: 17.375em;"> + <img class="w100" src="images/i_106.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 112.</span>—Cross +section of a cornstalk +(reduced): <i>v</i>, fibrovascular +bundles; <i>c</i>, cortex; +<i>p</i>, pith.</p></figcaption> +</figure> + +<p id="p-110"><b>110. Gross anatomy of a monocotyl stem.</b>—Obtain a +fresh cornstalk,—preferably one that has begun to tassel,—and +observe its external characters. How are the internodes +divided from one another? What +is the use of the very firm, smooth epidermis? +Notice a hollow, grooved channel +running down one side between the <em>joints</em>, +or nodes; does it occur in all of them? +Is it on the same side or on the opposite +sides of alternate internodes? Follow one +of these grooves to the node from which +it originates; what do you find there? +After studying the internal structure of the stalk, you will +understand why this groove should occur on the side of an +internode bearing a bud or fruit.</p> + +<p>Cut a cross section midway between two nodes, and observe +the composition of the interior; of what does the bulk +of it appear to consist? Notice the arrangement of the +little dots, like the ends of cut-off threads, that are scattered +through the pith; where are they most abundant, toward the +center or the circumference?</p> + +<figure class="figright illowp25" id="i_107" style="max-width: 12.5em;"> + <img class="w100" src="images/i_107.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 113.</span>—Vertical +section of cornstalk +(reduced): <i>g</i>, +groove; <i>c</i>, cortex; <i>v</i>, +fibrovascular bundles +mingled with parenchyma; +<i>b</i>, bud; <i>n</i>, +node.</p></figcaption> +</figure> + +<p>Make a vertical section through one of the nodes. Cut a +thin slice of the pith, hold it up to the light, and examine<span class="pagenum" id="Page_97">[Pg 97]</span> +with a hand lens. Observe that it is composed of a number +of oblong cells packed together like bricks in a wall. These +are filled with protoplasm and cell sap, and constitute what is +known to botanists as the <i>parenchyma</i> or +fundamental tissue from which all the other +tissues are derived. Apply the iodine test; +in what parts does starch occur most abundantly?</p> + +<p>Draw out one of the woody threads running +through the pith. Break away a bit of +the epidermis, and see how very closely they +are packed on its inner surface. Trace the +course of the veins in the bases of the leaves; +find their point of union with the stem; +with what part of it do they appear to be +continuous? Has this anything to do with +the greater abundance of fibers near the epidermis? +Can you follow the fibers through +the nodes, or do they become confused and intermixed with +other threads there? (If a stalk of sugar cane can be +obtained, the ring of scars left by the vascular bundles as +they pass from the leaves into the stem will be seen beautifully +marked just above the nodes.)</p> + +<p>If there is an eye or bud at the node, see if any of +the threads go into it. Can you account now for the depression +that occurs in the internode above the eye?</p> + +<p>Make drawings of both cross and vertical sections, showing +the points brought out in your examination of the cornstalk.</p> + +<p id="p-111"><b>111. The vascular system.</b>—To find out the use of the +threads that you have been tracing, examine a piece of a +living stem that has stood in red ink for three to twenty-four +hours. Notice the course the coloring fluid has taken; what +would you infer from this as to the use of the woody fibers?</p> + +<p>These threads constitute what is called the <em>vascular system</em> +of the stem, because they are made up of <em>vessels</em> or <em>ducts</em>, +along which the sap is conveyed from the roots to the leaves<span class="pagenum" id="Page_98">[Pg 98]</span> +and back from the leaves to the parts where it is needed after +it has contributed to the elaboration of food.</p> + +<p>On account of this double line of communication which +they have to maintain, the vascular threads, or <em>bundles</em>, as +they are technically called, are double; one part composed +of larger vessels, carrying water up, the other consisting of +smaller ones, bringing back the food. Can you give a reason +for their difference in size?</p> + +<figure class="figright illowp20" id="i_108" style="max-width: 12.5em;"> + <img class="w100" src="images/i_108.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 114.</span>—Longitudinal +section +through the stem +of a palm, showing +the curved course of +the fibrovascular +bundles (<span class="smcap">Gray</span>, <i>after</i> +<span class="smcap">Falkenberg</span>).</p></figcaption> +</figure> + +<p id="p-112"><b>112. Woody monocotyls.</b>—Examine sections of yucca, +smilax, or of palmetto from the handle of a fan, and compare +them with your sketches of the cornstalk. +In which are the vascular fibers most abundant? +Which is the toughest and strongest? +Why? Trace the course of the leaf fibers +from the point of insertion to the interior. +How does it differ from that of the fibers +in a cornstalk?</p> + +<p id="p-113"><b>113. Growth of monocotyl stems.</b>—After +tracing the course of the leaf veins at the +nodes of the cornstalk, you will have no +difficulty in identifying these veins as part of +the vascular system. In jointed stems like +those of the corn and sugar cane and other +grasses, their intercalation between the vascular +bundles of the stem takes place, as we +have seen, at the nodes, forming the hard +rings known as joints; but in other monocotyls +the fibers entering the stem from the +leaves usually tend first downward, toward the interior +(<a href="#i_108">Fig. 114</a>), then bend outward, toward the surface, where they +become entwined with others and form the tough, inseparable +cortex that gives to palmetto and bamboo stems their great +strength. Generally, monocotyl stems do not increase in diameter +after a certain point, and as they can contain only a +limited number of vascular fibers, they are incapable of supporting +an extended system of leaves and branches. Hence +plants of this class, with a few exceptions, like smilax and +asparagus, are characterized by simple, columnar stems and +a limited spread of leaves. Such plant forms are admirably +adapted by their structure to the purposes of mechanical +support. It is a well-known law of mechanics that a hollow +cylinder is a great deal stronger than the same mass would +be in solid form, as may easily be tested by the simple experiment +of breaking in your fingers a cedar pencil and a +joint of cane or a stem of smilax of the same weight. In +stems that may be technically classed as solid in structure, +like the corn and palmetto, the interior is so light compared +with the hard epidermis that the result is practically a hollow +cylinder.</p> + +<p><span class="pagenum" id="Page_99">[Pg 99]</span></p> + +<figure class="figcenter illowp51" id="i_109" style="max-width: 50em;"> + <img class="w100" src="images/i_109.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 4.</span>—Forest of bamboo, showing the tall, straight, branchless habit of +monocotyl stems.</p></figcaption> +</figure> + + +<p><span class="pagenum" id="Page_100">[Pg 100]</span></p> + +<p id="p-114"><b>114. Minute study of a monocotyl stem.</b>—Place under +the microscope a very thin transverse section of a cornstalk. +The little dots that looked like +the cut ends of threads to the +naked eye will now appear as +the complex group of cells shown in <a href="#i_110">Fig. 115</a>. The same parts +are shown longitudinally in <a href="#i_110a">Fig. 116</a>. As seen in cross section,<span class="pagenum" id="Page_101">[Pg 101]</span> +their arrangement suggests a grotesque resemblance to +the face of an old woman wearing a pair of enormous spectacles +and surrounded by a cap frill of netting with very wide +meshes. These are parenchyma cells, <i>f</i>, <i>f</i>, <a href="#i_110">Fig. 115</a>, and +constitute the greater portion of the living tissues.</p> + +<table><tr> +<td class='tdc vab'> +<figure class="figcenter illowp90" id="i_110" style="max-width: 38.6875em;"> + <img class="w100" src="images/i_110.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 115.</span>—Transverse section through +the fibrovascular bundle of a cornstalk: +<i>a</i>, annular tracheid; <i>sp</i>, spiral tracheid; +<i>m</i> and <i>m′</i>, ducts; <i>l</i>, air space; <i>v</i>, sieve +tubes; <i>s</i>, companion cells; <i>vg</i>, strengthening +fibers; <i>cp</i>, bast; <i>f</i>, <i>f</i>, parenchyma.</p></figcaption> +</figure> +</td><td class='tdc vab'> +<figure class="figcenter illowp90" id="i_110a" style="max-width: 40.0625em;"> + <img class="w100" src="images/i_110a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 116.</span>—Vertical section of the same; +<i>a</i> and <i>a′</i>, rings of a decomposed annular +tracheid; <i>v</i>, sieve tubes; <i>s</i>, companion +cells; <i>cp</i>, bast; <i>l</i>, air space; <i>vg</i>, strengthening +tissue; <i>sp</i>, spiral duct.</p></figcaption> +</figure> +</td></tr></table> + +<p>The two large openings, <i>m</i>, <i>m′</i>, that represent the spectacles, +are ducts for carrying water <em>up</em> the stem. They are called +pitted ducts on account of the bordered pits which cover +their outer surface. The two smaller openings between and +slightly below the pitted ducts are also vessels for carrying +liquids up the stem. The lower one, <i>a</i>, is called the annular +<i>tracheid</i> because its tube is strengthened by rings on the +inside. The upper, smaller one, <i>sp</i>, is known as the spiral +tracheid, because its walls are reinforced by spiral thickenings. +Can you think what is the use of these strengthening contrivances +in the walls of conducting cells? (Suggestion: What +is the use of the spiral wire on a garden hose?) The large, +irregular opening below the ducts is an air space. What is +its object? Why has it no surrounding wall?</p> + +<p>Next look above the ducts for a group of rhomboidal or +hexagonal cells, <i>v</i>, <i>v</i>, with smaller ones, <i>s</i>, between them. The +larger of these are <em>sieve tubes</em>, the smaller +ones, <em>companion cells</em>. The sieve tubes +carry sap <em>down</em> the stem after it has been +made into food by the leaves. They get +their name from the sievelike openings +between the connecting walls of the cells +which form them—as if a row of pepper +boxes with perforations at both top and +bottom were placed end to end, so as to +form a long tube divided into compartments +by perforated walls. Can you give a reason why the +cells of ducts that carry elaborated nutriment should have a +more open line of communication than those carrying crude +sap? [<a href="#p-56">56</a> (2).] Which one of the organic food substances was +shown by <a href="#exp-39">Exp. 39</a> to be unable, or nearly so, to pass through<span class="pagenum" id="Page_102">[Pg 102]</span> +the cell wall by osmosis? [<a href="#p-56">56</a> (4).] The +conducting cells are surrounded by a mass +of strengthening fibers separating them +from the parenchyma, <i>f</i>, and constituting +with them a <em>fibrovascular bundle</em>. The +larger vessels, <i>m</i>, <i>m′</i>, <i>a</i>, and <i>sp</i>, compose +the <i>xylem</i>, the harder, more woody part +of the bundle, and the smaller ones, <i>v</i>, <i>s</i>, +the <i>phloëm</i>, or softer part. Notice also +that there is no parenchyma in contact +with the xylem and phloëm in the fibrovascular +bundles of a monocotyl, to supply +material for new growth, but they are +entirely surrounded by a sheath of strengthening +tissue, whence such bundles are said +to be <em>closed</em>, and are incapable of further +growth by the addition of new cells.</p> + +<table class='autotable'><tr><td class='tdc'> +<figure class="figcenter illowp50" id="i_111" style="max-width: 17.75em;"> + <img class="w100" src="images/i_111.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 117.</span>—Horizontal +view of the sieve tube +of a gourd stem, showing +perforations.</p></figcaption> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp50" id="i_112" style="max-width: 21.625em;"> + <img class="w100" src="images/i_112.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 118.</span>—Side +view of the sieve +tube of a gourd stem: +<i>pr</i>, protoplasm layer; +<i>u</i>, albuminous contents, +forming mucilaginous +strand.</p></figcaption> +</figure></td></tr></table> + + + +<h4 id="CH_IV_III_B">B. <span class="smcap">Herbaceous Dicotyls</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Young stems of sunflower, hollyhock, burdock, ragweed, +cocklebur, castor bean, or any large herbaceous plant. In schools unprovided +with compound microscopes, the minute anatomy can be studied +with some degree of profit by the aid of pictures.</p> +</div> + +<p id="p-115"><b>115. Gross anatomy.</b>—Examine the outside of a young +stem of sunflower, burdock, or other herbaceous dicotyl. +Notice whether it is smooth, or roughened with hairs, scales, +ridges, or grooves. If hairy, observe the nature of the hairs, +whether bristly, downy, sticky, etc. Notice the color of the +epidermis, whether uniform, or splotched or striped with +other colors, as, for example, jimson weed, and pigweed +(amarantus). If there are any buds, branches, or flower +stems, notice where they originate; what is the angle between +the leaf and stem called? <a href="#p-100">(100.)</a></p> + +<p>Make a transverse cut through a portion of the stem that +has stood for a time in coloring fluid and examine with a lens. +Four regions can easily be distinguished: (1) the epidermis,<span class="pagenum" id="Page_103">[Pg 103]</span> +<i>e</i>, <a href="#i_113">Fig. 119</a>; (2) the primary cortex, <i>c</i>; (3) a ring of fibrovascular +bundles, <i>f</i>; and (4) a central cylinder of parenchyma, +<i>p</i>. In some specimens there will be a fifth region, the +pith, which will appear in +the section as a white circular +spot in the center of +the parenchyma.</p> + +<figure class="figright illowp30" id="i_113" style="max-width: 39.75em;"> + <img class="w100" src="images/i_113.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 119.</span>—Transverse section of a +very young stem of burdock, showing fibrovascular +bundles not completely united +into a ring: <i>e</i>, epidermis; <i>c</i>, primary cortex; +<i>f</i>, a ring of fibrovascular bundles; +<i>p</i>, central cylinder of parenchyma.</p></figcaption> +</figure> + +<p>In specimens a little older +than the one shown in <a href="#i_113">Fig. +119</a>, a narrow circular line +will be seen running through +the ring of bundles nearly +midway between their inner +and outer extremities, connecting +them into an unbroken +circle around the +central cylinder. This is +the <i>cambium</i> layer, which supplies the vascular region with +materials for new growth, and thus enables dicotyl stems to +increase in diameter by the successive addition of fresh +vascular rings from year to year.</p> + +<p>Examine in the same way a vertical section, and find the +parts corresponding to those shown in <a href="#i_113">Fig. 119</a>. Make enlarged +sketches of both sections, labeling the various parts +observed.</p> + +<p id="p-116"><b>116. Minute structure of a dicotyl stem.</b>—Place successively +under a high power of the microscope thin transverse +and longitudinal sections of the stem just examined, or +such other specimen as the teacher may provide. Bring one +of the fibrovascular bundles into the field, and try to make +out the parts shown in <a href="#i_114">Figs. 120 and 121</a>. The corresponding +parts in the two sections are indicated by the same letters. +Notice the cortex, <i>R</i>, on the outside and the pith, <i>M</i>, on the +inside; between these, the cambium, <i>C</i>, the <i>xylem</i>, or woody +tissue, included between the radiating lines <i>X</i>, and the newer +tissues composing the <i>phloëm</i> between the lines <i>P</i>. The +cambium and pith, which includes the medullary rays so conspicuous +in perennial stems, are composed of live parenchyma +cells, from which alone growth can take place; they +are the active part of the stem. The xylem contains the +large vessels, <i>t</i> and <i>s</i>, that convey water <em>up</em> the stem, together +with the wood fibers, <i>h</i>. These are the permanent tissues. +After completing their growth the cells of the xylem gradually +lose their protoplasm, and all vitality ceases. Even the +cell sap disappears, and sometimes the walls of the ducts are +disintegrated, leaving a mere air space like that shown at <i>l</i> in +<a href="#i_110">Figs. 115</a> and <a href="#i_110a">116</a>. The dead cells and tissues, however, are +by no means useless. They constitute the heartwood that +is so valuable for timber, and serve an important purpose as +a mechanical support for the stem. The phloëm contains +on its outer face a mass of hard fibers, <i>b</i>, called bast, and +toward the interior, the sieve tubes, <i>sb</i>, with a number of +smaller vessels that convey <em>down</em> the stem the sap containing +the food made in the leaves. It is separated from the cortex +by the bundle sheath, <i>e</i>, and on its other side, from the exterior +face of the xylem by the cambium, <i>C</i>. In this position +the growing cambium adds new cells to the inner side of the +phloëm, and to the outer side of the xylem, so that the former +grows on its inner face and the latter on its outer. In perennial +plants, as new rings are added to the xylem from season +to season, the older ones die and are changed into heartwood, +which thus gradually increases in thickness till in some of the +giant redwoods and eucalypti, it may attain a diameter of +thirty-five or forty feet. In the phloëm, on the other hand, +as new cells are added from within, the older ones are +gradually changed into hard bast, <i>b</i>, then into bark, and +are finally sloughed off and fall to the ground. It is this +free line of communication with the active cambium that +enables dicotyl stems to grow on indefinitely, the sheath, <i>e</i>, +being formed on the exterior face of the bundles only, leaving +the other free, whence they are said to be <em>open</em>.</p> + +<p><span class="pagenum" id="Page_104">[Pg 104]</span></p> + +<figure class="figcenter illowp75" id="i_114" style="max-width: 50em;"> + <img class="w100" src="images/i_114.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 120-121.</span>—Transverse and longitudinal sections of a fibrovascular bundle +in the stem of a sunflower. The two sections are lettered to correspond: <i>M</i>, pith +(parenchyma); <i>X</i>, xylem region; <i>P</i>, phloëm; <i>R</i>, cortex; <i>s</i>, spiral ducts; <i>s′</i>, annular +ducts; <i>t</i>, <i>t</i>, pitted ducts; <i>C</i>, cambium between the phloëm and xylem regions; <i>sb</i>, +sieve tubes; <i>b</i>, bast; <i>e</i>, bundle sheath; <i>ic</i>, cambium (parenchyma) cells; <i>h</i>, wood fibers.</p></figcaption> +</figure> + + +<p>Make drawings of cross and vertical sections of a dicotyl +<span class="pagenum" id="Page_105">[Pg 105]</span> +stem as it appears under the microscope, labeling correctly +all the parts observed. Show the shape and relative size of +the different cells. Compare +your drawings with +those made in your study +of monocotyl stems, and +write in your notebook the +essential points of difference +between the two.</p> + +<p><span class="pagenum" id="Page_106">[Pg 106]</span></p> + +<figure class="figcenter illowp75" id="i_116" style="max-width: 50em;"> + <img class="w100" src="images/i_116.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 122.</span>—Internal structure of a pine stem, showing longitudinal section of a +fibrovascular bundle through a medullary ray, <i>sm</i>, <i>sm′</i>; <i>s</i>, tracheids; <i>t</i>, bordered +pits, surface view; <i>c</i>, cambium; <i>v</i>, sieve tubes; <i>vt</i>, sieve pits, analogous to the +sieve plates in dicotyl stems.</p></figcaption> +</figure> + +<figure class="figcenter illowp60" id="i_116a" style="max-width: 40.125em;"> + <img class="w100" src="images/i_116a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 123.</span>—Internal structure of a pine +stem, showing transverse section of a tracheid: +<i>i</i>, cell walls; <i>m</i>, intermediate layer +between walls of adjoining cells; <i>m′</i>, intercellular +space here occupied by substance +of intermediate layer; <i>b</i>, bordered pit in +section at right angles to the surface; <i>t</i>, +membrane for closing the pit canal.</p></figcaption> +</figure> + +<p id="p-117"><b>117. The stems of conifers</b>, +the group of Gymnosperms +to which the pine +belongs, do not differ greatly +from those of dicotyls, the +chief difference being that +the vascular bundles contain +tracheids only, corresponding +to the smaller vessels of<span class="pagenum" id="Page_107">[Pg 107]</span> +the phloëm, <i>s</i> and <i>s′</i>, shown in <a href="#i_114">Fig. 121</a>. These tracheids +have large sunken places in their walls, called bordered pits +(<a href="#i_116a">Fig. 123</a>), closed by a very thin membrane through which +water and dissolved food materials can more readily percolate. +In all other essentials, the internal structure of pine +stems is like that of dicotyls. (See <a href="#i_118">Plate 5</a>.)</p> + + +<h4 id="CH_IV_III_C">C. <span class="smcap">Woody Stemmed Dicotyl</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Elm, basswood, mulberry, leatherwood, and pawpaw +show the bast well; sassafras, slippery elm, and (in spring) hickory and +willow show the cambium; grape and trumpet vine, the ducts. Some +of the specimens used should be placed in coloring fluid from 3 to 8 hours +before the lesson begins. The rate at which the liquid is absorbed varies +with the kind of stem and the season. It is more rapid in spring and slower +in winter. If a cutting stands too long in the fluid, the dye will gradually +percolate through all parts of it; care should be taken to guard against this.</p> +</div> + +<figure class="figright illowp35" id="i_117" style="max-width: 18.75em;"> + <img class="w100" src="images/i_117.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 124.</span>—Part of a +young China tree shoot, +showing, <i>A</i>, lenticels; <i>B</i>, +leaf scar; <i>C</i>, <i>C</i>, traces left +by the broken ends of +fibrovascular bundles that +passed from the stem into +the leaf. Natural size.</p></figcaption> +</figure> + +<p id="p-118"><b>118. The external layer.</b>—While the primary structures, +as shown in the last section, are essentially the same in all +dicotyl stems, the continued yearly +growth of perennials causes them to develop +a number of secondary structures +and variations of detail that differentiate +them in a marked degree from soft-stemmed +annuals. Take a piece of a +three-year-old shoot of cherry, horse +chestnut, or any convenient hardwood +tree, and notice that the soft, green +epidermis has given place to a thicker, +harder, and usually darker colored bark. +Notice the presence of lenticels <a href="#p-106">(106)</a> and +their porous, corky texture for the admission +of air to the interior. They +are slightly raised above the surface of +the bark, and are usually round, or +more or less elongated in different directions, +according as they are stretched vertically or horizontally +by the growth of the axis. The characteristic markings +of birch bark, which make it so ornamental, are due to the +lenticels. In most trees they disappear on the older parts, +where the bark is constantly breaking away and sloughing off.</p> + +<p><span class="pagenum" id="Page_108">[Pg 108]</span></p> + +<figure class="figcenter illowp51" id="i_118" style="max-width: 57em;"> + <img class="w100" src="images/i_118.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 5.</span>—Stem of a conifer, <i>Sequoia gigantea</i>, Mariposa Grove, California. The +first branch, 6 feet in diameter, leaves the parent trunk 125 feet above the ground. +The photographer sitting on one of the exposed roots affords a good standard for +comparison. The tree is noted for its massive limbs. The smaller trees in the +background show the characteristic mode of branching in trees of this class.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_109">[Pg 109]</span></p> + +<p id="p-119"><b>119. Internal structures.</b>—Cut a transverse section +through your specimen, and notice under the epidermis a +greenish layer of young bark; beneath this a layer of rather +tough, stringy bast fibers, and beyond these a harder woody +substance that constitutes the bulk of the interior; within this, +at the very center of the axis, we find a cylinder of lighter +texture, the pith, or medulla, occupying the place of the soft +parenchyma which fills this space in very young stems.</p> + +<p>Between the woody axis and the bark notice a more or +less soft and juicy ring.</p> + +<p id="p-120"><b>120. The cambium layer.</b>—This is not always easily +distinguishable with a hand lens, but is conspicuous in the +stems of sassafras, slippery elm, and aristolochia. If some +of these cannot be obtained, the presence of the cambium +can be recognized by observing the tendency of most stems +to “bleed,” when cut, between the wood and bark. The +reason for this is because the cambium is the active part of +the stem, in which growth is taking place, and consequently +it is most abundantly supplied with sap. In spring, especially, +it becomes so full of sap that if a rod of hickory +or elder is pounded, the pulpy cambium is broken up and the +bark may be slipped off whole from the wood.</p> + +<p id="p-121"><b>121. Medullary rays.</b>—Observe the whitish, silvery lines +that radiate in every direction from the center, like the +spokes of a wheel from the hub. These are the medullary +rays, and consist of threads of pith that serve as lines of communication +between the “central cylinder” and the growing +cambium layer. In old stems the central pith frequently +disappears and its office is filled by the medullary rays, which +become quite conspicuous.</p> + +<figure class="figcenter illowp75" id="i_120" style="max-width: 50em;"> + <img class="w100" src="images/i_120.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 125, 126.</span>—Cross sections of twigs: 125, section across a young twig of box +elder, showing the four stem regions: <i>e</i>, epidermis, represented by the heavy bounding +line; <i>c</i>, cortex; <i>w</i>, vascular cylinder; <i>p</i>, pith; 126, section across a twig of box elder +three years old, showing three annual growth rings, in the vascular cylinder. The +radiating lines (<i>m</i>), which cross the vascular region (<i>w</i>), represent the pith rays, the +principal ones extending from the pith to the cortex (<i>c</i>). (<i>From</i> <span class="smcap">Coulter’s</span> “Plant +Relations.”)</p></figcaption> +</figure> + +<p id="p-122"><b>122. Structural regions of a woody stem.</b>—Sketch cross +and vertical sections of your specimen, as seen under the lens, +labeling the different parts. Refer to <a href="#i_120">Figs. 125, 126</a>, if you<span class="pagenum" id="Page_110">[Pg 110]</span> +have any difficulty in distinguishing the parts. In a year-old +shoot (<a href="#i_120">Fig. 125</a>), the structural regions correspond closely to +those shown in <a href="#i_113">Fig. 119</a>, except that the ring of fibrovascular +bundles is here compact and woody, and crossed by the +radiating lines of the medullary rays. In a three-year-old +shoot (<a href="#i_120">Fig. 126</a>), the main divisions are the same, but the +soft parenchyma of the central cylinder is replaced by the +pith, and the vascular ring is composed of three layers corresponding +to the three years of growth. In general, mature +dicotyl stems may be said to include four well-defined regions: +(1) the epidermis, or the bark; (2) the cortex, made +up of bast and certain other tissues; (3) the cambium; +(4) the woody vascular cylinder, made up of concentric +rings, each representing a year’s growth. The pith, or medulla, +constitutes a fifth region, but is obvious only in young +stems. Notice the little pores or cavities that dot the woody +part in the cross section; where are they largest and most +abundant? How are the rings marked off from one another?<span class="pagenum" id="Page_111">[Pg 111]</span> +These pores are the sections of ducts. They are very large +in the grapevine, and a cutting two or three years old will +show them distinctly. Examine sections of a twig that has +stood in red ink from three to twelve hours, and observe the +course the fluid has taken. How does this accord with the +facts observed in your study of the conducting tissues in +monocotyl and herbaceous stems? (<a href="#p-111">111</a>, <a href="#p-115">115</a>, <a href="#p-116">116</a>.)</p> + +<figure class="figright illowp20" id="i_121" style="max-width: 12.5em;"> + <img class="w100" src="images/i_121.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 127.</span>—Diagram +illustrating the +annual growth of +dicotyledons.</p></figcaption> +</figure> + +<p id="p-123"><b>123. The rings</b> into which the woody cylinder is divided +mark the yearly additions to the growth of the stem, which +increases by the constant accession of new +material to the outside of the permanent +tissues <a href="#p-116">(116)</a>. The cambium constantly +advances outward, beginning every spring +a new season’s growth, and leaving behind +the ring of ducts and woody fibers made +the year before. As the work of the plant is +most active and its growth most vigorous +in spring, the largest ducts are formed then, +the tissue becoming closer and finer as the +season advances, thus causing the division +into annual rings that is so characteristic of +woody dicotyl stems. Each new stratum of +growth is made up of the fibrovascular +bundles that supply the leaves and buds and +branches of the season. In this way we see +that the increase of dicotyl trunks and +branches is approximately in an elongated +cone (<a href="#i_121">Fig. 127</a>), the number of rings gradually diminishing +toward the top till at the terminal bud of each bough it is +reduced to a single one, as in the stems of annuals.</p> + +<p>Sometimes a late autumn, succeeding a very dry summer, +will cause trees to take on a second growth, and thus form two +layers of wood in a single season. On this account we cannot +always rely absolutely upon the number of rings in estimating +the age of a tree, though the method is sufficiently +exact for all practical purposes.</p> + +<p><span class="pagenum" id="Page_112">[Pg 112]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Old Fort Moultrie near Charleston was built originally of palmetto +logs; was this good engineering or not? Why? <a href="#p-113">(113.)</a></p> + +<p>2. Explain the advantages of structure in a culm of wheat; a stalk of +corn; a reed. <a href="#p-113">(113.)</a></p> + +<p>3. Would the same quality be of advantage to an oak? Why, or why +not?</p> + +<p>4. Is it of any advantage to the farmer that grain straw is so light?</p> + +<p>5. Explain why boys can slip the bark from certain kinds of wood in +spring to make whistles. <a href="#p-120">(120.)</a></p> + +<p>6. Why cannot they do this in autumn or winter? <a href="#p-123">(123.)</a></p> + +<p>7. Name some of the plants commonly used for this purpose.</p> + +<p>8. Is the spring, after the buds begin to swell, a good time to prune +fruit trees and hedges? <a href="#p-120">(120.)</a></p> + +<p>9. What is the best time, and why?</p> + +<p>10. Why are grapevines liable to bleed to death if pruned too late in +spring? (<a href="#p-120">120</a>, <a href="#p-123">123</a>.)</p> + +<p>11. Why are nurserymen, in grafting, so careful to make the cambium +layer of the graft hit that of the stock? <a href="#p-120">(120.)</a></p> + +<p>12. In calculating the age of a tree or bough from the rings of annual +growth, should we take a section from near the tip, or from the base? +Why? <a href="#p-123">(123.)</a></p> +</div> + + +<h3 id="CH_IV_IV">IV. THE WORK OF STEMS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Leafy shoots of grape, balsam, peach, or other active +young stems; a cutting of willow, currant, or any kind of easily rooting +stem. Two bottles of water and some linseed or cottonseed oil.</p> + +<figure class="figright illowp30" id="i_123" style="max-width: 32.75em;"> + <img class="w100" src="images/i_123.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 128.</span>—Experiment showing +that moisture is thrown off by the +leaves of plants.</p></figcaption> +</figure> + +<p id="exp-58"><span class="smcap">Experiment 58. Do the leaves have any active part in effecting +the movement of sap in the stem?</span>—Take two healthy young shoots of +the same kind—grape, peach, corn, tropæolum, calla lily absorb rapidly. +Trim the leaves from one shoot and close the cut surfaces with a little vaseline +or gardener’s wax to prevent loss of water by evaporation. Place the +lower end of each in a glass jar or tumbler filled to the same height with +water. Cut off <em>under water</em> a half inch from the bottom of each shoot, +to get a fresh absorbing surface. This is necessary because exposure to +air for even a second greatly hinders absorption by permitting the entrance +of air into the severed ends of the ducts. Pour a little oil on the water in +both jars to prevent evaporation. (Do not use kerosene; it is injurious +to plants.) At the end of twenty-four hours, which vessel has lost the +more water? How do you account for the difference?</p> + +<p><span class="pagenum" id="Page_113">[Pg 113]</span></p> + +<p id="exp-59"><span class="smcap">Experiment 59. What becomes of the water that goes into the +leaves?</span>—Cover the top of the vessel containing the leafy twig used in the +last experiment with a piece of cardboard, +having first cut a slit in one side, +as shown in <a href="#i_123">Fig. 128</a>, so that it can be +slid into place without injuring the +stem. Invert over the twig a tumbler +that has first been thoroughly dried, +and leave in a warm, dry place. After +an hour or two, what do you see on the +<em>inside</em> of the tumbler? Where did the +moisture come from?</p> + +<figure class="figleft illowp20" id="i_123a" style="max-width: 13em;"> + <img class="w100" src="images/i_123a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 129.</span>—A +twig which had been +kept standing in +water after the removal +of a ring of +cortical tissue: <i>a</i>, +level of the water; +<i>b</i>, swelling formed at +the upper denudation; +<i>c</i>, roots.</p></figcaption> +</figure> + +<p id="exp-60"><span class="smcap">Experiment 60. Through what +part of the stem does the sap flow +upward?</span>—Remove a ring of the cortical +layer from a +twig of any readily +rooting dicotyl, +such as willow, +being careful to +leave the woody +part, with the cambium, intact. Place the end <em>below</em> +the cut ring in water, as shown in <a href="#i_123a">Fig. 129</a>. The leaves +above the girdle will remain fresh. How is the water +carried to them? How does this agree with the +movement of red ink observed in 115 and 122?</p> + +<p id="exp-61"><span class="smcap">Experiment 61. Through what part does the +sap come down?</span>—Next prune away the leaves and +protect the girdled surface with tin foil, or insert it +below the neck of a deep bottle to prevent evaporation, +and wait until roots develop. Do they come more +abundantly from above or below the decorticated +ring?</p> +</div> + +<p id="p-124"><b>124. The three principal functions of the +stem</b> are:—(1) to serve as a mechanical support +and framework for binding the other +organs together and bringing them into the best attainable +relations with light and air; (2) as a water carrier, or pipe +line, for conveying the sap from the roots to the parts where +it is needed; and (3) as a receptacle for the storage of foods.</p> + +<p><span class="pagenum" id="Page_114">[Pg 114]</span></p> + +<p id="p-125"><b>125. Movement of water.</b>—It has already been shown +(71, 111) that a constant interchange of liquid is taking place +through the stem, between the roots, where it is absorbed from +the ground, and the leaves, where it is used partly in the manufacture +of food. Just what causes the rise of sap in the stem +is one of the problems of vegetable physiology that botanists +have not yet been able to +solve. There are, however, +certain forces at +work in the plant, which, +though they may not account +for all the phenomena +of the movement, +undoubtedly influence +them to a great extent. +From experiments 58-61, +we can obtain an +idea of what some of +these forces may be.</p> + +<figure class="figcenter illowp50" id="i_124" style="max-width: 50em;"> + <img class="w100" src="images/i_124.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 130.</span>—The stump of a large oak that +was injured by lightning many years ago. The +interior is completely decayed, leaving only +a hollow shell of living tissue, from which +branches continue to put forth leaves year +after year.</p></figcaption> +</figure> + +<p id="p-126"><b>126. Direction of the +current.</b>—These experiments +show that the upward +movement of crude +sap toward the leaves is +mainly through the ducts +in the woody portion of +the stem, while the downward +flow of elaborated +sap from the leaves takes +place chiefly through the +soft bast and certain other vessels of the cortical layer. The +action of the leaves in giving off part of the water absorbed, as +shown in <a href="#exp-59">Exp. 59</a>, probably has also an important influence +on the course of sap movement. If loss of water takes place +in any organ through growth or other cause, the osmotic flow +of the thinner sap from the roots will set in that direction.</p> + +<p><span class="pagenum" id="Page_115">[Pg 115]</span></p> + +<p id="p-127"><b>127. Ringing fruit trees.</b>—The course of the sap explains +why farmers sometimes hasten the ripening of fruit by the +practice of <em>ringing</em>. As the food material cannot pass below +the denuded ring, the parts above become gorged, and a process +of forcing takes place. The practice, however, is not to +be commended, except in rare cases, as it generally leads to +the death of the ringed stem. The portion below the ring +can receive no nourishment from above, and will gradually +be so starved that it cannot even act as a carrier of crude +sap to the leaves, and so the whole bough will perish.</p> + +<figure class="figright illowp30" id="i_125" style="max-width: 25em;"> + <img class="w100" src="images/i_125.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 131.</span>—Diagram showing +general movement of sap.</p></figcaption> +</figure> + +<p id="p-128"><b>128. Sap movement not circulation.</b>—It must not be +supposed that this flow of sap in plants is analogous to the +circulation of the blood in animals, +though frequently spoken of in popular +language as the “circulation of +the sap.” There is no central organ +like the heart to regulate its flow, and +the water taken up by the roots does +not make a continual circuit of the +plant body as the blood does of ours, +but is dispersed by a process of general +diffusion, partly into the air through +the leaves and partly through the plant +body as food, wherever it is needed. +<a href='#i_125'>Figure 131</a> gives a good general idea +of the movement of sap in trees, the +arrows indicating the direction of the +movement of the different substances.</p> + +<p id="p-129"><b>129. Unexplained phenomena.</b>—Though the forces +named above undoubtedly exert a powerful influence over +sap movement, their combined action has not been proved +capable of lifting the current to a height of more than 200 +feet, while in the giant redwoods of California and the towering +blue gums of Australia, it is known to reach a height of +more than 400 feet. The active force exerted by the cell +protoplasm has been suggested as an efficient cause, but as<span class="pagenum" id="Page_116">[Pg 116]</span> +the upward flow takes place through the cells of the xylem, +which contain no protoplasm <a href="#p-116">(116)</a>, this explanation is inadequate, +and we must be content, in the present state of our +knowledge, to accept the fact as one which science has yet to +account for.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why will a leafy shoot heal more quickly than a bare one? (<a href="#p-125">125</a>, +<a href="#p-126">126</a>; <a href="#exp-58">Exp. 58</a>.)</p> + +<p>2. Why does a transverse cut heal more slowly than a vertical one? +(<a href="#p-126">126</a>, <a href="#p-127">127</a>.)</p> + +<p>3. Why does a ragged cut heal less rapidly than a smooth one?</p> + +<p>4. Why does the formation of wood proceed more rapidly as the amount +of water given off by the leaves is increased? (<a href="#p-126">126</a>; <a href="#exp-59">Exp. 59</a>.)</p> + +<p>5. Why do nurserymen sometimes split the cortex of young trees in +summer to promote the formation of wood? (<a href="#p-116">116</a>, <a href="#p-118">118</a>.)</p> + +<p>6. What is the advantage of scraping the stems of trees?</p> + +<p>7. Explain the frothy exudation that often appears at the cut ends of +firewood, and the singing noise that accompanies it. [<a href="#p-120">120</a>, <a href="#p-124">124</a> (2).]</p> + +<p>8. Of what advantage is it to high climbing plants, like grape and +trumpet vine (<i>Tecoma</i>), to have such large ducts? (<a href="#p-111">111</a>, <a href="#p-116">116</a>, <a href="#p-122">122</a>.)</p> + +<p>9. Why is the process of layering more apt to be successful if the shoot +is bent or twisted at the point where it is desired to make it root? (<a href="#p-127">127</a>; +<a href="#exp-60">Exps. 60</a>, <a href="#exp-61">61</a>.)</p> + +<p>10. Why do oranges become dry and spongy if allowed to hang on the +tree too long? (<a href="#p-72">72</a>, <a href="#p-126">126</a>; <a href="#exp-60">Exps. 60</a>, <a href="#exp-61">61</a>.)</p> + +<p>11. Why will corn and fodder be richer in nourishment if, at harvest, +the whole stalk is cut down and both fodder and grain are allowed to +mature upon it? (<a href="#p-126">126</a>, <a href="#p-127">127</a>; <a href="#exp-60">Exps. 60</a>, <a href="#exp-61">61</a>.)</p> + +<p>12. Is the injury done to plants by freezing due, as a general thing, +to mechanical, or to chemical action? <a href="#p-33">(33.)</a></p> + +<p>13. Why in pruning a branch is it best to make the cut just above a +bud? (<a href="#exp-60">Exps. 60</a>, <a href="#exp-61">61</a>.)</p> + +<p>14. Why is the rim of new bark, or callus, that forms on the upper side +of a horizontal wound, thicker than that on the lower side? (126, 127; +<a href="#exp-60">Exps. 60</a>, <a href="#exp-61">61</a>.)</p> + +<p>15. Why is it that the medicinal or other special properties of plants +are found mostly in the leaves and bark, or in the parts immediately +under the bark? (<a href="#p-120">120</a>, <a href="#p-126">126</a>.)</p> + +<p>16. Why does twisting the footstalk of a bunch of grapes, just before +ripening, make them sweeter? (<a href="#p-127">127</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_117">[Pg 117]</span></p> + +<figure class="figcenter illowp54" id="i_127" style="max-width: 50em;"> + <img class="w100" src="images/i_127.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 6.</span>—A white oak, one of the monarchs of the dicotyl type. The owner of +the ground on which this noble tree stands left a clause in his will bequeathing it in +perpetuity a territory of 8 feet in every direction from its base. Refer to <a href="#p-89">89</a> and +decide whether such an amount of standing room is sufficient to secure the preservation +of this beautiful object.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_118">[Pg 118]</span></p> + +<div class="blockquot"> + +<p>17. Is it a mere superstition to drive nails into the stems of plum and +peach trees to make them bear larger or more abundant fruit? (<a href="#p-126">126</a>, <a href="#p-127">127</a>.)</p> + +<p>18. Why is a living corn stalk heavier than a dry one? <a href="#p-124">(124.)</a></p> + +<p>19. Why is a stalk of sugar cane heavier than one of corn? Suggestion: +Which is the heavier, pure water, or water holding solids in solution?</p> +</div> + + +<h3 id="CH_IV_V">V. WOOD STRUCTURE IN ITS RELATION TO INDUSTRIAL USES</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Select from the billets of wood cut for the fire, sticks of +various kinds; hickory, ash, oak, chestnut, maple, walnut, cherry, pine, +cedar, tulip tree, all make good specimens. Red oak shows the medullary +rays well. Get sticks of green wood, if possible, and have them planed +smooth at the ends. Collect also, where they can be obtained, waste bits +of dressed lumber from a carpenter or joiner. If nothing better is available, +any pieces of unpainted woodwork about the schoolroom will furnish +subjects for study.</p> +</div> + +<p id="p-130"><b>130. Detailed structure of a woody stem.</b>—Select a +good-sized billet of hard wood, and count the rings of annual +growth. How old was the tree or the bough from which it +was taken? Was its growth uniform from year to year? +How do you know? Are the rings broader, as a general +thing, toward the center or the circumference? How do +you account for this? Is each separate ring of uniform +thickness all the way round? Mention some of the circumstances +that might cause a tree to grow less on one side +than on the other. Are the rings of the same thickness in +all kinds of wood? Which are the more rapid growers, those +with broad or with narrow rings? Do you notice any difference +in the texture of the wood in rapid and in slow growing +trees? Which makes the better timber as a general +thing, and why?</p> + +<p id="p-131"><b>131. Heartwood and sapwood.</b>—Notice that in some +of your older specimens (cedar, black walnut, barberry, +black locust, chestnut, oak, Osage orange, show the difference +distinctly) the central part is different in color and texture +from the rest. This is because the sap gradually abandons +the center (<a href="#p-116">116</a>, <a href="#p-123">123</a>) to feed the outer layers, where growth +in dicotyls takes place; hence, the outer part of the stem +usually consists of sapwood, which is soft and worthless as +timber, while the dead interior forms the durable heartwood +so prized by lumbermen. The heartwood is useful to +the plant principally in giving strength and firmness to the +axis. It will now be seen why girdling a stem,—that is, chipping +off a ring of the softer parts all round, will kill it, while +vigorous and healthy trees are often seen with the center of +the trunk entirely hollow.</p> + +<p><span class="pagenum" id="Page_119">[Pg 119]</span></p> + +<figure class="figcenter illowp50" id="i_129" style="max-width: 50em;"> + <img class="w100" src="images/i_129.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 132.</span>—Cross section through a black oak, showing heartwood +and sapwood. (<i>From</i> <span class="smcap">Pinchot</span>, U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<figure class="figcenter illowp60" id="i_129a" style="max-width: 50em;"> + <img class="w100" src="images/i_129a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 133.</span>—Vertical section through a black oak. (<i>From</i> <span class="smcap">Pinchot</span>, +U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<figure class="figright illowp40" id="i_130" style="max-width: 25em;"> + <img class="w100" src="images/i_130.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 134-136.</span>—Diagrams of sections +of timber: 134, cross section; +135, radial; 136, tangential. (<i>From</i> +<span class="smcap">Pinchot</span>, U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_120">[Pg 120]</span></p> + +<p id="p-132"><b>132. Different ways of cutting.</b>—In studying the vertical +arrangement of stems, two sections are necessary, a radial and +a tangential one. The former passes along the axis, splitting +the stem into halves (<a href="#i_130">Fig. 135</a>); the latter cuts between the +axis and the perimeter, splitting +off a segment from one +side (<a href="#i_130">Fig. 136</a>). The appearance +of the wood used in carpentry +and joiner’s work is due +largely to the manner in which +the planks are cut.</p> + +<p id="p-133"><b>133. The cross cut.</b>—The +section seen at the end of a log +(<a href="#i_129">Figs. 132</a>, <a href="#i_130">134</a>) is called by +carpenters a cross cut. It +passes at right angles to the +grain of the wood, and severs what important structures? +(<a href="#p-116">116</a>, <a href="#p-119">119</a>, <a href="#p-122">122</a>.) Examine a cross cut at the end of a rough +plank, or the top of +a stump or an old +fence post, and tell +why this kind of cut +is seldom used in +carpentry.</p> + +<figure class="figright illowp40" id="i_130a" style="max-width: 25em;"> + <img class="w100" src="images/i_130a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 137.</span>—Tangential section of mountain ash, showing +ends of the medullary rays.</p></figcaption> +</figure> + +<p id="p-134"><b>134. The tangent +cut</b> is so called because +it is made at +right angles to the<span class="pagenum" id="Page_121">[Pg 121]</span> +radius of a log. Repeat the geometrical +principle upon which such +a cut is described as “tangential.” +It passes through the medullary +rays and the annual rings diagonally +(<a href="#i_130">Fig. 136</a>), and is the cheapest way +of cutting timber, since the entire +log is made into planks and there +is no waste except the “slabs” and +“edgings,” as shown in <a href="#i_131">Fig. 138</a>. +The cut ends of the medullary rays +appear on the surface as small lines +or slits (<a href="#i_130a">Fig. 137</a>), and give to this +kind of plank its peculiar graining. +The wavy or “watered” +appearance of the annual rings +(<a href="#i_129a">Figs. 133</a>, <a href="#i_130">136</a>, <a href="#i_132">140</a>, <a href="#i_132a">141</a>), so often +seen in cheap furniture and in the woodwork of cheaply +constructed houses, is caused by the tangential cut, which +strikes them at various angles.</p> + +<table class='autotable'> +<tr><td class='tdc'> +<figure class="figcenter illowp80" id="i_131" style="max-width: 35em;"> + <img class="w100" src="images/i_131.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 138.</span>—Diagram to show +the common method of sawing a +log. The circles represent rings +of annual growth: <i>R</i>, <i>R</i>, diameter +of the log; <i>r</i>, <i>r</i>, <i>r</i> and <i>t</i>, <i>t</i>, <i>t</i>, +boards cut perpendicular to it, +giving for the two or three central +ones radial, for the others, +tangential, cuts. The waste portions +are the “slabs” and “edgings,” +shown in the dark segments +at <i>R</i>, <i>R</i>, and the small +triangular blocks, <i>e</i>, <i>e</i>, <i>e</i>.</p></figcaption> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp80" id="i_131a" style="max-width: 35em;"> + <img class="w100" src="images/i_131a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 139.</span>—Diagram illustrating +the “quartered” cut: <i>d</i>, <i>d</i> and +<i>d′</i>, <i>d′</i>, radial cuts (diameters) by +which the log is “quartered”; +<i>c</i>, center of the log; <i>r</i>, <i>r</i>, radii +passing through the middle of +each quarter, parallel to which +the planks <i>t</i>, <i>t</i>, <i>t</i> are cut. The +circles represent rings of annual +growth.</p></figcaption> +</figure></td></tr></table> + +<p id="p-135"><b>135. The radial, or quartered cut</b>, +familiar to most of us in the “quartered +oak” of commerce, passes +through the center of the log and +cuts the rings of annual growth perpendicularly, +giving it the “striped” +appearance (<a href="#i_130">Fig. 135</a>) seen in the +best woodwork. It gets its name +from the practice of dealers in first +sawing a log into quarters and then +cutting parallel to the radius passing +through the middle of each +quarter, as shown in <a href="#i_131a">Fig. 139</a>. In +this way each cut strikes the rings +perpendicularly, but except in the +case of very large logs, only narrow<span class="pagenum" id="Page_122">[Pg 122]</span> +planks can be obtained in this manner. A better way of +treating small logs is shown in <a href="#i_131">Fig. 138</a>, where the three +central planks, <i>r</i>, <i>r</i>, <i>r</i>, on and near the diameter, will give the +“quartered” effect, while the rest can be used for the cheaper +tangential cuttings. Examine a piece of quartered board, or +a log of wood that has been split down the center, and notice +that the medullary rays appear as silvery bands or plates +(<a href="#i_132">Figs. 140</a>, <a href="#i_132a">141</a>). This is because the cut runs parallel to +them. It is the medullary rays chiefly that give to commercial +woods their characteristic graining. Knots, buds, and +other adventitious causes also influence it in various degrees.</p> + +<figure class="figcenter illowp75" id="i_132" style="max-width: 54em;"> + <img class="w100" src="images/i_132.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 140.</span>—Sections of sycamore wood: <i>a</i>, tangential; <i>b</i>, radial; +<i>c</i>, cross. (<i>From</i> <span class="smcap">Pinchot</span>, U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<figure class="figcenter illowp70" id="i_132a" style="max-width: 52em;"> + <img class="w100" src="images/i_132a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 141.</span>—Section of white pine wood. (<i>From</i> <span class="smcap">Pinchot</span>, +U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<figure class="figright illowp25" id="i_133" style="max-width: 15.5em;"> + <img class="w100" src="images/i_133.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 142.</span>—Section +of tree trunk showing +knot.</p></figcaption> +</figure> + +<p id="p-136"><b>136. The swelling and shrinking of timber.</b>—The capacity +possessed by certain substances of bringing about an<span class="pagenum" id="Page_123">[Pg 123]</span> +increase of volume by the absorption of liquids is termed +<em>imbibition</em>. Care must be taken not to confound imbibition +with capillarity. (<a href="#exp-53">Exp. 53</a>.) When liquids are carried +into a body by capillary attraction, they +merely fill up vacant spaces already existing +between small particles of the substance, +and therefore do not cause any swelling or +increase in size. When imbibition takes +place, the <em>molecules</em>, or chemical units of the +liquid, force their way between those of the +imbibing substance, and thus, in making +room for themselves, bring about an increase +in volume of the imbibing body. +To this cause is due the alternate swelling and shrinking of +timber in wet and dry weather.</p> + +<figure class="figright illowp30" id="i_133a" style="max-width: 21.25em;"> + <img class="w100" src="images/i_133a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 143-144.</span>—Diagrams +of tree trunks, showing +knots of different ages: +143, from tree grown in +the open; 144, from tree +grown in a dense forest.</p></figcaption> +</figure> + +<p id="p-137"><b>137. Knots.</b>—Look for a billet with a knot in it. Notice +how the rings of growth are disturbed +and displaced in its neighborhood. If +the knot is a large one, it will itself +have rings of growth. Count them, and +tell what its age was when it ceased to +grow. Notice where it originates. +Count the rings from its point of origin +to the center of the stem. How old was +the tree when the knot began to form? +Count the rings from the origin of the +knot to the circumference of the stem; +how many years has the tree lived since +the knot was formed? Does this agree +with the age of the knot as deduced +from its own rings? As the tree may +continue to live and grow indefinitely +after the bough which formed the knot +died or was cut away, there will probably be no correspondence +between the two sets of rings, especially in the +case of old knots that have been covered up and embedded in<span class="pagenum" id="Page_124">[Pg 124]</span> +the wood. The longer a dead branch remains on a tree the +more rings of growth will form around it before covering it up, +and the greater will be the disturbance caused by it. Hence, +timber trees should be pruned while very young, and the +parts removed should be cut as close as possible to the main +branch or trunk. Sometimes knots injure lumber very much +by falling out and leaving the holes that are often seen in pine +boards. In other cases, however, when the knots are very +small, the irregular markings caused by them add greatly +to the beauty of the wood. The peculiar marking of bird’s-eye +maple is caused by abortive buds buried in the wood.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Is the swelling of wood a physical or a physiological process?</p> + +<p>2. Does wood swell equally with the grain and across it? (Suggestion: +test by keeping a block under water for 10 to 20 days, measuring its dimensions +before and after immersion.)</p> + +<p>3. In building a fence, what is the use of “capping” the posts? <a href="#p-133">(133.)</a></p> + +<p>4. In laying shingles, why are they made to touch, if the work is done +in wet weather, and placed somewhat apart, if in dry weather? <a href="#p-136">(136.)</a></p> + +<p>5. What is the difference between timber and lumber? Between a +plank and a board? Between a log, stick, block, and billet?</p> + +<p>6. Why does sapwood decay more quickly than heartwood? <a href="#p-131">(131.)</a></p> + +<p>7. Explain the difference between osmosis, diffusion, capillarity, and +imbibition. (<a href="#p-9">9</a>, <a href="#p-56">56</a>, <a href="#p-57">57</a>, <a href="#p-136">136</a>; <a href="#exp-53">Exp. 53</a>.)</p> +</div> + + +<h3 id="CH_IV_VI">VI. FORESTRY</h3> + +<p id="p-138"><b>138. Practical bearings.</b>—This part of our subject is +closely related to lumbering and forestry. The business of +the lumberman is to manufacture growing trees into merchantable +timber, and to do this successfully he must understand +enough about the structure of wood to cut his boards +to the best advantage, both for economy and for bringing out +the grain so as to produce the most desirable effects for +ornamental purposes.</p> + +<p><span class="pagenum" id="Page_125">[Pg 125]</span></p> + +<figure class="figcenter illowp48" id="i_135" style="max-width: 53em;"> + <img class="w100" src="images/i_135.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 7.</span>—Timber tree spoiled by standing too much alone in early youth. +Notice how the crowded young timber in the background is righting itself, the lower +branches dying off early from overshading, leaving tall, straight, clean boles. (<i>From</i> +<span class="smcap">Pinchot</span>, U. S. Dept. of Agr.)</p></figcaption> +</figure> + +<figure class="figright illowp40" id="i_136" style="max-width: 25em;"> + <img class="w100" src="images/i_136.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 145.</span>—After the forest fire.</p></figcaption> +</figure> + +<p id="p-139"><b>139. Forestry has for its object</b>: (1) the preservation +and cultivation of existing forests; (2) the planting of new +ones, or the reforestation of tracts from which the timber has +been destroyed. Forests may be either <em>pure</em>, that is, composed +mainly of one +kind of tree, as a pine +or a fir wood; or <em>mixed</em>, +being made up of a variety +of different growths, +as are most of our common +hardwood forests.</p> + +<p><span class="pagenum" id="Page_126">[Pg 126]</span></p> + +<figure class="figright illowp30" id="i_136a" style="max-width: 25em;"> + <img class="w100" src="images/i_136a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 146.</span>—Oyster fungus on linden.</p></figcaption> +</figure> + +<p id="p-140"><b>140. Enemies of the +forest.</b>—The first step +in the preservation of +our forests is to know +the dangers to be +guarded against. The +chief of these are: +(1) fires; (2) the ignorance +or recklessness of +man in cutting for +commercial purposes; +(3) fungi; (4) injurious insects; (5) sheep, hogs, and other +animals that eat the seeds and the young, tender growth.</p> + +<p id="p-141"><b>141. How to protect the +forests.</b>—The annual destruction +of forests by fires +probably exceeds that from +all other causes combined. +The only effectual safeguard +against this danger is watchfulness +on the part of <em>everybody</em>. +We can each one of +us help in this work by at +least being careful ourselves +never to kindle a fire in the +woods without taking every +precaution against its<span class="pagenum" id="Page_127">[Pg 127]</span> +spreading. A single match, or the glowing stump of a cigar, +carelessly thrown among dry leaves or grass, may start a +conflagration that will destroy millions of dollars’ worth of +standing timber.</p> + +<p>To prevent the spread of fungi, dead trees should be removed, +and broken or decayed branches trimmed off and the +cut surfaces painted. Birds which destroy insects should be +protected; sheep and hogs should be kept out, and dead +leaves left on the ground to cover the roots and fertilize the +soil with the humus created by their decay. Finally, none +but mature trees should be cut for industrial purposes, and +the cutting ought to be done in such a way that the young +surrounding growth will not be injured by the falling +trunks.</p> + +<p id="p-142"><b>142. The usefulness of forests.</b>—Aside from the value +of their products, forests are useful in many other ways. +They influence climate beneficially by acting as windbreaks, +by giving off moisture (<a href="#exp-58">Exp. 58</a>), by shading the soil, and +thus preventing too rapid evaporation. Their roots also +help to retain the water in the soil, and by this means tend +to prevent the washing of the land by heavy rains and to +restrain the violence of freshets.</p> + +<p id="p-143"><b>143. Forests and water supply.</b>—It is especially important +that the watershed of any region should be well +protected by forests, to prevent contamination of the streams +and to insure an unfailing supply of water by checking the +escape of the rainfall from the soil.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Explain the difference between a forest, grove, copse, wood, woodland.</p> + +<p>2. In pruning a tree why ought the branch to be cut as close to the stock +as possible? <a href="#p-137">(137.)</a></p> + +<p>3. Name the principal timber trees of your neighborhood. What gives +to each its special value?</p> + +<p>4. Name six trees that produce timber valuable for ornament; for +toughness and strength.</p> + +<p><span class="pagenum" id="Page_128">[Pg 128]</span></p> + +<p>5. Which is the better for timber, a tree grown in the open, or one +grown in a forest, and why? (<a href="#i_135">Plate 7</a>.)</p> + +<p>6. What are the objects to be attained in pruning timber trees? Orchard +and ornamental trees?</p> + +<p>7. Is the outer bark of any use to a tree, and if so, what?</p> + +<p>8. Why should pruning not be done in wet weather? [<a href="#p-140">140</a> (3), <a href="#p-141">141</a>.]</p> + +<p>9. Why should vertical shoots be cut off obliquely? [<a href="#p-133">133</a>, <a href="#p-140">140</a> (3), +<a href="#p-141">141</a>.]</p> +</div> + + +<h4 id="CH_IV_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>(1) Make a study of the various climbing plants of your neighborhood +with reference to their modes of ascent, and the effect, injurious, or other, +upon the plants to which they attach themselves. Note the origin and +position of tendrils, and try to make out what modification has taken +place in each case. Consider the twining habit in reference to parasitism, +especially in the case of soft-stemmed twiners when brought into contact +with soft-stemmed annuals. Observe the various habits of stem growth: +prostrate, declined, ascending, etc., and decide what adaptation to circumstances +may have influenced each case.</p> + +<p>(2) Notice the shape of the different stems met with, and learn to +recognize the forms peculiar to certain of the great families. Observe +the various appliances for defense and protection with which they are +provided, and try to find out the meaning of the numerous grooves, ridges, +hairs, prickles, and secretions that are found on stems. Always be on the +alert for modifications, and learn to recognize a stem under any disguise, +whether thorn, tendril, foliage, water holder, rootstock, or tuber.</p> + +<p>(3) Note the color and texture of the bark of the different trees you see +and learn to distinguish the most important kinds:</p> + +<div class="blockquot"> + +<p>(<i>a</i>) scaly—peeling off annually in large plates, as sycamore, shagbark-hickory;</p> + +<p>(<i>b</i>) fibrous—detached in stiff threads and fibers, as grape;</p> + +<p>(<i>c</i>) fissured—split into large, irregular cracks by the growth of the +stem in thickness, as oak, chestnut, and most of our large forest +trees;</p> + +<p>(<i>d</i>) membranous—separating in dry films and ribbons, as common +birch (<i>Betula alba</i>).</p> +</div> + +<p>Observe the difference in texture and appearance of the bark on old +and young boughs of the same species. Try to account for the varying +thickness of the bark on different trees and on different parts of the same +tree. Notice the difference in the timber of the same species when grown +in different soils, at different ages of the tree, and in healthy and weakly +specimens. Find examples of self-pruning trees (<a href="#i_135">Plate 7</a>), and explain +how the pruning was brought about.</p> + +<p><span class="pagenum" id="Page_129">[Pg 129]</span></p> + +<p>(4) Select a small plot, about a fourth of an acre, of any wooded tract +in your neighborhood, and make a study of all the trees and shrubs it contains. +Make a list of the different kinds, with the number of each. Take +note of those that show themselves, by vigor and abundance of growth, +best adapted to the situation. These are the “climax” or dominant +vegetation of the plot. Find out, if you can, to what cause their superiority +is due.</p> +</div> + +<p><span class="pagenum" id="Page_130">[Pg 130]</span></p> + +<figure class="figcenter illowp90" id="i_140" style="max-width: 50em;"> + <img class="w100" src="images/i_140.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 8.</span>—The American elm—a perfect type of deliquescent branching.</p></figcaption> +</figure> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_131">[Pg 131]</span></p> + + +<h2 class="nobreak" id="CH_V">CHAPTER V. BUDS AND BRANCHES</h2> +</div> + +<h3 id="CH_V_I">I. MODES OF BRANCHING</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For determinate growth, have twigs of an alternate and +an opposite-leaved plant showing well-developed terminal buds: hickory, +sweet gum, cottonwood, poplar, chestnut, are good examples of the +first; maple, ash, horse-chestnut, viburnum, of the second; for the two-forked +kind, mistletoe, buckeye, horse-chestnut, jimson weed, lilac. For +showing indefinite growth: rose, willow, sumach, and ailanthus are good +examples. Gummy buds, like horse-chestnut and poplar, should be +soaked in warm water before dissecting, to soften the gum; the +same treatment may be applied when the scales are too brittle to be +handled without breaking. Buds with heavy fur on the scales cannot +very well be studied in section; the parts must be taken out and +examined separately.</p> +</div> + +<table class='autotable'> +<tr><td class='tdc'> +<figure class="figcenter illowp100" id="i_141" style="max-width: 14em;"> + <img class="w100" src="images/i_141.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 147.</span>—Diagram +of excurrent +growth.</p></figcaption> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp100" id="i_141a" style="max-width: 19.5em;"> + <img class="w100" src="images/i_141a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 148.</span>—Diagram +of deliquescent growth.</p></figcaption> +</figure></td></tr></table> + + +<p id="p-144"><b>144. Modes of branching.</b>—Compare the arrangement +of the boughs on a pine, cedar, magnolia, etc., with those +of the elm, maple, apple, or any of our +common deciduous trees. Draw a diagram +of each, showing the two modes of growth. +The first represents the +<em>excurrent</em> kind, from the +Latin <i>excurrere</i>, to run +out; the second, in which +the trunk seems to divide +at a certain point +and flow away, losing +itself in the branches, +is called <em>deliquescent</em>, +from the Latin <i lang="la">deliquescere</i>, +to melt or flow away. +The great majority of stems, as a little observation will +show, present a combination of the two modes.</p> + +<p><span class="pagenum" id="Page_132">[Pg 132]</span></p> + +<figure class="figright illowp20" id="i_142" style="max-width: 12.5em;"> + <img class="w100" src="images/i_142.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 149.</span>—Winter +twig of sugar maple: +<i>t</i>, terminal bud; <i>ax</i>, +axillary buds; <i>ls</i>, leaf +scars; <i>tr</i>, leaf traces; +<i>l</i>, lenticels; <i>rs</i>, ring of +scars left by bud scales +of preceding season.</p></figcaption> +</figure> + +<p id="p-145"><b>145. Terminal and axillary buds.</b>—Notice the large bud +at the end of a twig of hickory, sweet gum, beech, cottonwood, +etc. This is called the <em>terminal</em> bud because it terminates +its branch. Notice the scars left by the leaves of +the season as they fell away, and look for small buds just +above them. These are <em>lateral</em>, or <em>axillary</em>, buds, so called +because they spring from the axils of the leaves. How +many leaves did your twig bear? What +difference in size do you notice between +the terminal and lateral buds?</p> + +<p id="p-146"><b>146. The leaf scars.</b>—Examine the leaf +scars with a hand lens, and observe the +number and position of the little dots in +them. Ailanthus, varnish tree, sumach, +and China tree show these very distinctly. +They are called <em>leaf traces</em>, and mark the +points where the fibrovascular bundles +from the leaf veins passed into the stem. +Look on the bark, or epidermis, for lenticels.</p> + +<p id="p-147"><b>147. Bud scales and scars.</b>—Notice the +stout, hard scales by which the winter buds +are covered in most of our hardy trees and +shrubs. Remove these from the terminal +one of your specimen, and notice the ring +of scars left around the base. Look lower down on your +twig for a ring of similar scars left from last year’s bud. +Is there any difference in the appearance of the bark above +and below this ring? If so, what is it, and how do you account +for it? Is there more than one of these rings of scars +on your twig, and if so, how many? How old is the twig +and how much did it grow each year? Has its growth been +uniform, or did it grow more in some years than in others?</p> + +<figure class="figright illowp25" id="i_143" style="max-width: 15.25em;"> + <img class="w100" src="images/i_143.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 150.</span>—Diagram +of opposite bud +scales.</p></figcaption> +</figure> + +<p id="p-148"><b>148. Arrangement and use of the scales.</b>—Notice the +manner in which the scales overlap so as to “break joints,” +like shingles on the roof of a house. Where the leaves are +opposite, the manner of superposition is very simple. Remove<span class="pagenum" id="Page_133">[Pg 133]</span> +the scales one by one, representing the number and +position of the pairs by a diagram after the model given in +<a href="#i_143">Fig. 150</a>. In the bud of an alternately branched twig the +order will be different, and the diagram must be varied accordingly. +Do you observe any difference +as to size and texture between the outer +and inner scales? Notice how the former +inclose the tenderer parts within like a +protecting wall. In cold climates the outer +scales are frequently +coated with gum, as in +the horse-chestnut, for +greater security against +the weather. The hickory and various +other trees have the inner scales covered +with fur or down that envelops the tender +bud like a warm blanket.</p> + +<p id="p-149"><b>149. Nature of the scales.</b>—The position +of the scales shows that they occupy +the place of leaves or of some part of a +leaf. In expanding buds of the lilac and +many other plants, they can be found in +all stages of transition, from scales to +true leaves. In the buckeye and horse-chestnut, +they will easily be recognized +as modified leaf stalks (<a href="#i_143a">Fig. 151</a>). In the +tulip tree, magnolia, India rubber tree, +fig, elm, and many others, they represent +appendages called <em>stipules</em>, often found at +the bases of leaves. (See 165, 166.) In +this case a pair of scales is attached with +each separate leaflet, and as the growing axis lengthens in +spring, they are carried apart by the elongation of the internodes +so that the scars are separated, a pair at each node, +making rings all along the stem, as shown in <a href="#i_144">Fig. 152</a>, instead +of having them compacted into bands at the base of<span class="pagenum" id="Page_134">[Pg 134]</span> +the bud. These scars are sometimes very persistent, and +in the common fig and magnolia may often be traced on +stems six to eight years old. Do they furnish +any indication as to the relative age of the +different parts of the stem, like the bands of +scars on twigs of horse-chestnut and hickory? +Give a reason for your answer. (<a href="#i_144">Fig. 152</a>.)</p> + +<table class='autotable double-image'> +<tr> +<td class='tdc'> +<figure class="figcenter illowp50" id="i_143a" style="max-width: 20.5em;"> + <img class="w100" src="images/i_143a.jpg" alt=""> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp50" id="i_144" style="max-width: 20.5em;"> + <img class="w100" src="images/i_144.jpg" alt=""> +</figure></td></tr> +<tr> +<td class='tdl caption'><p><span class="smcap">Fig. 151.</span>—Development +of the parts of +the bud in the buckeye. +(<i>After</i> <span class="smcap">Gray</span>.)</p></td> +<td class='tdl caption'><p><span class="smcap">Fig. 152.</span>—Stem +of tulip tree: <i>s</i>, <i>s</i>, +scars left by stipular +scales; <i>l</i>, <i>l</i>, leaf scars.</p></td></tr> +</table> + +<p id="p-150"><b>150. Different rates of growth.</b>—Notice +the very great difference between branches +in this respect. Sometimes the main stem +will have lengthened from twenty to fifty +centimeters or more in a single season, while +some of the lateral ones will have grown +but an inch or two in four or five seasons. +One reason for this is because the terminal +bud, being on the great trunk line of sap +movement, gets a larger share of nourishment +than the others, and being stronger +and better developed to begin with, starts out in life with +better chances of success.</p> + +<p>Make a drawing of your specimen, showing all the points +brought out in the examination just made. Cut sections +above and below a set of bud scars and count the rings of +annual growth in each section. What is the age of each? +How does this agree with your calculation from the number +of scar clusters left by the bud scales?</p> + +<p id="p-151"><b>151. Irregularities.</b>—Take a larger bough of the same +kind that you have been studying, and observe whether the +arrangement of branches on it corresponds with the arrangement +of buds on the twig. Did all the buds develop into +branches? Do those that did develop all correspond in size +and vigor? If all the buds developed, how many branches +would a tree produce every year?</p> + +<p>In the elm, linden, beech, hornbeam, hazelnut, willow, and +various other plants, the terminal bud always dies and the +one next in order takes its place, giving rise to the more or<span class="pagenum" id="Page_135">[Pg 135]</span> +less zigzag axis that generally characterizes trees of these +species. (<a href="#i_145">Fig. 153</a>.)</p> + +<figure class="figright illowp30" id="i_145" style="max-width: 28.75em;"> + <img class="w100" src="images/i_145.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 153.</span>—Bud development +of beech: <i>a</i>, as it is, many buds +failing to develop; <i>b</i>, as it would +be if all the buds were to live.</p></figcaption> +</figure> + +<p id="p-152"><b>152. Forked stems.</b>—Take a twig of buckeye, horse-chestnut, +or lilac, and make a careful +sketch of it, showing all the +points that were brought out in the +examination of your previous specimen. +Which is the larger, the lateral +or the terminal bud? Is their +arrangement alternate or opposite? +What was the leaf arrangement? +Count the leaf traces in the scars; +are they the same in all? If all the +buds had developed into branches, +how many would spring from a +node? Look for the rings of scars +left by the last season’s bud scales. +Do you find any twig of more +than one year’s growth, as measured by the scar rings?</p> + +<figure class="figleft illowp15" id="i_145a" style="max-width: 12.5em;"> + <img class="w100" src="images/i_145a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 154.</span>—Two-forked +twig of horse-chestnut.</p></figcaption> +</figure> + +<p>Look down between the forks of a branched stem for a +round scar. This is not a leaf scar, as we can see by its +shape, but one left by the last season’s +flower cluster. The flower, as we know, +dies after perfecting its fruit, and so a +flower bud cannot continue the growth of +its axis as other buds do, but has just the opposite +effect and stops all further growth in +that direction. Hence, stems and branches +that end in a flower bud cannot continue +to develop their main axis, but their growth +is usually carried on, in alternate-leaved +stems, by the nearest lateral bud, or in +opposite-leaved ones, by the nearest pair +of buds. In the first case there results the zigzag spray +characteristic of such trees as the beech and elm (<a href="#i_146">Fig. 155</a>, +<i>B</i>); in the second, the two-forked, or <em>dichotomous</em> branching,<span class="pagenum" id="Page_136">[Pg 136]</span> +exemplified by the buckeye, horse-chestnut, jimson weed, +mistletoe, and dogwood (<a href="#i_146">Fig. 155</a>, <i>A</i>).</p> + +<p>Draw a diagram of the buckeye, or +other dichotomous stem, as it would be if +all the buds developed into branches, and +compare it with your diagrams of excurrent +and deliquescent growth. Draw diagrams +to illustrate the branching of the elm, +beech, lilac, linden, rose, maple, or their +equivalents.</p> + +<figure class="figleft illowp20" id="i_146" style="max-width: 14.625em;"> + <img class="w100" src="images/i_146.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 155.</span>—Diagrams +of two-forked +branching. The +pointed bodies in the +forks shows where terminal +flower buds or +flower clusters have +changed the direction +of growth.</p></figcaption> +</figure> + +<p id="p-153"><b>153. Definite and indefinite annual +growth.</b>—The presence or absence of terminal +buds gives rise to another important +distinction in plant development—that +of <em>definite</em> and <em>indefinite</em> annual growth. +Compare with any of the twigs just +examined, a branch of rose, honey locust, +sumac, mulberry, etc., and note the difference +in their modes of termination. The first kind, where +the bough completes its season’s increase in a definite time +and then devotes its energies to developing a strong +terminal bud to begin the next year’s work with, are said +to make a <em>definite or determinate annual growth</em>. Those +plants, on the other hand, which make no provision for +the future, but continue to grow till the cold comes +and literally nips them in the bud, are <em>indefinite</em>, or <em>indeterminate</em> +annual growers. Notice the effect of this habit +upon their mode of branching. The buds toward the end +of each shoot, being the youngest and tenderest, are most +readily killed off by frost or other accident, and hence new +branches spring mostly from the older and stronger buds +near the base of the stem. It is their mode of branching that +gives to plants of this class their peculiar bushy aspect. +Such shrubs generally make good hedges on account of their +thick undergrowth. The same effect can be produced artificially +by pruning.</p> + +<p><span class="pagenum" id="Page_137">[Pg 137]</span></p> + +<figure class="figright illowp40" id="i_147" style="max-width: 38.5em;"> + <img class="w100" src="images/i_147.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 156.</span>—A mixed wood in winter, showing +the trend of the branches.</p></figcaption> +</figure> + +<p id="p-154"><b>154. Differences in the branching of trees.</b>—We are now +prepared to understand something about the causes of that +endless variety in the +spread of bough and +sweep of woody spray +that makes the winter +woods so beautiful. +Where the terminal bud +is undisputed monarch +of the bough, as in the +pine and fir, or where it +is so strong and vigorous +as to overpower its +weaker brethren and +keep the lead, as in the +magnolia, tulip tree, and holly, we have excurrent growth. +In plants like the oak and apple, where all the buds have +a more nearly equal chance, the lateral +branches show more vigor, and the result +is either deliquescent growth, or a mixture +of the two kinds. In the elm and beech, +where the usurping pseudo-terminal bud +keeps the mastery, but does not completely +overpower its fellows, we find the long, +sweeping, delicate spray characteristic of +those species. Examine a sprig of elm, +and notice further that the flower buds are +all down near the base of the stem, while +the leaf buds are near the tip. The chief +development of the season’s growth is thus +thrown toward the end of the branch, giving +rise to that fine, feathery spray which +makes the elm an even more beautiful +object in winter than in summer (<a href="#i_148">Fig. 158</a>).</p> + +<p>An examination of the twigs of other trees will bring out the +various peculiarities that affect their mode of branching. The<span class="pagenum" id="Page_138">[Pg 138]</span> +angle, for instance, which a twig makes with its bough has a +great effect in shaping the contour of the tree. Compare in +this respect the elm and hackberry; +the tulip tree and willow; ash and hickory. +As a general thing, acute angles +produce slender, flowing effects; right +or obtuse angles, more bold and rugged +outlines.</p> + +<table class='autotable double-image'> +<tr> + <td class='tdc wd60'> + +<figure class="figcenter illowp34" id="i_147a" style="max-width: 16.75em;"> + <img class="w100" src="images/i_147a.jpg" alt="Fig. 157.—Winter +spray of ash, an opposite-leaved +tree."> +</figure> +</td> +<td class='tdc wd40'> +<figure class="figcenter illowp64" id="i_148" style="max-width: 18.75em;"> + <img class="w100" src="images/i_148.jpg" alt="Fig. 158.—Winter spray +of elm."> +</figure> +</td> +</tr> +<tr> +<td class='tdc captionx'><span class="smcap">Fig. 157.</span>—Winter +spray of ash, an opposite-leaved +tree.</td> +<td class='tdc caption'><span class="smcap">Fig. 158.</span>—Winter spray +of elm.</td> +</tr> +</table> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Has the arrangement of leaves on a twig +anything to do with the way a tree is branched? +(<a href="#p-145">145</a>, <a href="#p-151">151</a>, <a href="#p-152">152</a>.)</p> + +<p>2. Why do most large trees tend to assume +the excurrent, or axial, mode of growth if let +alone? (<a href="#p-150">150</a>, <a href="#p-154">154</a>.)</p> + +<p>3. If you wished to alter the mode of growth, or to produce what nurserymen +call a low-headed tree, how would you prune it? (<a href="#p-152">152</a>, <a href="#p-153">153</a>.)</p> + +<p>4. Would you top a timber tree? (<a href="#p-152">152</a>, <a href="#p-153">153</a>.)</p> + +<p>5. Are low-headed or tall trees best for an orchard? Why?</p> + +<p>6. Why is the growth of annuals generally indefinite?</p> + +<p>7. Name some trees of your neighborhood that are conspicuous for +their graceful winter spray.</p> + +<p>8. Name some that are characterized by sharpness and boldness of outline.</p> + +<p>9. Account for the peculiarities in each case.</p> +</div> + + +<h3 id="CH_V_II">II. BUDS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Expanding leaf and flower buds in different stages of +development; large ones show the parts best and should be used where +attainable. Some good examples for the opposite arrangement are +horse-chestnut, maple, lilac, ash; for the alternate: hickory, sweet gum, +balsam poplar, beech, elm. Where material is scarce, the twigs used in the +last section may be placed in water and kept till the buds begin to expand.</p> +</div> + +<p id="p-155"><b>155. Folding of the leaves.</b>—Remove the scales from a +bud of horse-chestnut nearly ready to open, and notice the +manner in which the young leaves are folded. This is called +<em>vernation</em>, or <em>prefoliation</em>, words meaning respectively “spring +condition” and “condition preceding the leaf.” Leaves +are packed in the bud so as to occupy the least space possible, +and in different plants they will be found folded in a great<span class="pagenum" id="Page_139">[Pg 139]</span> +many different ways, according to the shape +and texture of the leaf and +the space available for it in +the bud. When doubled back +and forth like a fan, or crumpled +and folded as in the +buckeye, horse-chestnut, and +maple, the vernation is <em>plicate</em> +(<a href="#i_149b">Figs. 160</a>, <a href="#i_149a">162</a>).</p> + +<table class='double-image autotable'> +<tr> +<td class='tdc'> +<figure class="figcenter illowp40" id="i_149" style="max-width: 16.5em;"> + <img class="w100" src="images/i_149.jpg" alt="Fig. 159.—Expanding +bud of English walnut, +showing twice conduplicate +vernation."> +</figure> +</td> +<td class='tdc'> +<figure class="figcenter illowp25" id="i_149b" style="max-width: 9.75em;"> + <img class="w100" src="images/i_149b.jpg" alt="Fig. 160.—A +partly expanded +leaf of beech, +showing plicate-conduplicate +vernation."> +</figure> +</td></tr> +<tr> +<td class='tdl caption'><p><span class="smcap">Fig. 159.</span>—Expanding +bud of English walnut, +showing twice conduplicate +vernation.</p></td> +<td class='tdl caption'><p><span class="smcap">Fig. 160.</span>—A +partly expanded +leaf of beech, +showing plicate-conduplicate +vernation.</p></td> +</tr> +</table> + +<p id="p-156"><b>156. Position of the flower +cluster.</b>—What do you find +within the circle of leaves? +Examine one of the smaller +axillary buds, and see if you find the same object within it. +If you are in any doubt as to what this object is, examine +a bud that is more expanded, and you will have no difficulty +in recognizing it as a rudimentary flower +cluster. Notice its position with reference +to the scales and leaves. If at the +center of the bud, it will, of course, terminate +its axis when the +bud expands, and the +growth of the branch +will culminate in the +flower. The branching +of any kind of stem +that bears a central +flower cluster must, +then, be of what order? +Compare your drawings +with the section of +a hyacinth bulb or +jonquil, and note the +similarity in position +of the flower clusters. +In a bud of the hickory,<span class="pagenum" id="Page_140">[Pg 140]</span> +walnut, oak, etc., the position of the +flower clusters is different from that of +flowers in the buds of lilac and horse-chestnut. +Look for a bud containing them, and +find out where they occur. Can the axis continue +to grow after flowering, in this kind of +stem? Give a reason for your answer. Make +sketches in transverse and longitudinal section +(see <a href="#i_149a">Figs. 162</a>, <a href="#i_149c">163</a>) of two different +kinds of buds, illustrating the terminal and +axillary position of the flower cluster.</p> + +<table class='autotable double-image'> +<tr><td class='tdc'> +<figure class="figcenter illowp30" id="i_149a" style="max-width: 20em;"> + <img class="w100" src="images/i_149a.jpg" alt="Figs. 161, 162.</span>—Buds +of maple: 161, vertical +section of a twig; 162, +cross section through +bud, showing folded +leaves in center and scales +surrounding them."> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp40" id="i_149c" style="max-width: 20em;"> + <img class="w100" src="images/i_149c.jpg" alt="Fig. 163.</span>—Vertical +section of hickory +bud: <i>a</i>, furry inner +scales; <i>b</i>, outer +scales; <i>l</i>, folded leaf; +<i>r</i>, receptacle."> +</figure> +</td></tr> +<tr> +<td class='tdl caption'><p><span class="smcap">Figs. 161, 162.</span>—Buds +of maple: 161, vertical +section of a twig; 162, +cross section through +bud, showing folded +leaves in center and scales +surrounding them.</p></td> +<td class='tdl caption'><p><span class="smcap">Fig. 163.</span>—Vertical +section of hickory +bud: <i>a</i>, furry inner +scales; <i>b</i>, outer +scales; <i>l</i>, folded leaf; +<i>r</i>, receptacle.</p></td> +</tr> +</table> + +<p id="p-157"><b>157. Dormant buds.</b>—A bud may often +lie dormant for months or even years, and +then, through the injury or destruction of its +stronger rivals, or some other favoring cause, +develop into a branch. Such buds are said +to be <em>latent</em> or <em>dormant</em>. The sprouts that +often put up from the stumps of felled trees +originate from this source.</p> + +<figure class="figright illowp29" id="i_150" style="max-width: 25em;"> + <img class="w100" src="images/i_150.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 164.</span>—Twig +of red maple, showing +supernumerary +bud, <i>b</i>; <i>rs</i>, ring of +scars left by last +year’s bud scales. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-158"><b>158. Supernumerary buds.</b>—Where more +than one bud develops at a node, as is so +often the case in the oak, maple, honey +locust, etc., all except the normal one in the +axil are <em>supernumerary</em> or <em>accessory</em>. These must not be confounded +with <em>adventitious</em> buds—those that occur elsewhere +than at a node.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Would protected buds be of any use to annuals? Why, or why not?</p> + +<p>2. Of what use is the gummy coating found on the buds of the horse-chestnut +and balm of Gilead? (<a href="#p-148">148</a>.)</p> + +<p>3. Can you name any plants the buds of which serve as food for man?</p> + +<p>4. How do flower buds differ in shape from leaf buds?</p> + +<p>5. At what season can the leaf bud and the flower bud first be distinguished? +Is it the same for all flowering plants?</p> + +<p>6. Watch the different trees about your home, and see when the buds +that are to develop into leaves and flowers the next season are formed in +each species.</p> +</div> + +<p><span class="pagenum" id="Page_141">[Pg 141]</span></p> + + +<h3 id="CH_V_III">III. THE BRANCHING OF FLOWER STEMS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Typical flower clusters illustrating the definite and +indefinite modes of inflorescence. Some of those mentioned in the text +are:—</p> + +<p>Indefinite: hyacinth, shepherd’s purse, wallflower, carrot, lilac, blue +grass, smartweed (<i>Polygonum</i>), wheat, oak, willow, clover.</p> + +<p>Definite: chickweed, spurge (<i>Euphorbia</i>), comfrey, dead nettle, etc. +Any examples illustrating the principal kinds of cluster will answer.</p> +</div> + +<p id="p-159"><b>159. Inflorescence</b> is a term +used to denote the position and +arrangement of flowers on the +stem. It is merely a mode of +branching, and follows the same +laws that govern the branching +of ordinary stems.</p> + +<p>The stalk that bears a flower +is called the <em>peduncle</em>. In a +cluster the main axis is the common +peduncle, and the separate +flower stalks are <em>pedicels</em>. A simple +leafless flower stalk that rises +directly from the ground, like +those of the dandelion and daffodil, +is called a <em>scape</em> (<a href="#i_151">Fig. 165</a>).</p> + + +<table class='autotable'> +<tr> +<td class='tdc'> +<figure class="figcenter illowp50" id="i_151" style="max-width: 37em;"> + <img class="w100" src="images/i_151.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 165.</span>—Solitary terminal +flower of a lily.</p></figcaption> +</figure> +</td><td class='tdc'> +<figure class="figcenter illowp100" id="i_151a" style="max-width: 19.5em;"> + <img class="w100" src="images/i_151a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 166.</span>—Indeterminate +inflorescence of moneywort. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> +</td></tr></table> + +<p id="p-160"><b>160. Two kinds of inflorescence.</b>—The +growth of flower stems, like that of leaf stems, +is of two principal kinds, definite and +indefinite, or, as it is frequently expressed, +determinate and indeterminate. +The simplest kind of each is +the solitary, a single flower either +terminating the main axis, as the +tulip, daffodil, trillium, magnolia, +etc., or springing singly from the axils, as the running periwinkle, +moneywort, and cotton.</p> + +<p><span class="pagenum" id="Page_142">[Pg 142]</span></p> + +<table class='autotable'> +<tr> +<td class='wd50'> +<figure class="figcenter illowp50" id="i_152" style="max-width: 30.9375em;"> + <img class="w100" src="images/i_152.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 167.</span>—Raceme +of milk vetch (<i>Astragalus</i>).</p></figcaption> +</figure> +</td><td class='wd50'> +<figure class="figcenter illowp100" id="i_152a" style="max-width: 25em;"> + <img class="w100" src="images/i_152a.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Fig, 168.</span>—Catkins of aspen.</p></figcaption> +</figure> +</td></tr></table> + +<p id="p-161"><b>161. Indeterminate inflorescence</b> is always axillary, +since the production of a terminal flower would stop further +growth in that direction and thus terminate the development +of the axis. The <em>raceme</em> is the typical +flower cluster of the indefinite sort. In +such an arrangement the oldest flowers +are at the lower nodes, new ones appearing +only as the axis lengthens and produces +new internodes. The little scale or +<em>bract</em> usually found at the base of the pedicel +in flower clusters of this sort is a reduced +leaf, and the fact that the flower +stalk springs from the axil shows it to be +of the essential nature of a branch. +When the flowers are sessile and crowded +on the axis in various degrees, the cluster +produced may be a <em>spike</em>, as seen in the +plantain, knotweed, etc., or a <em>head</em>, like +that of the clover, buttonwood, and sycamore. +The <em>catkins</em> that form the characteristic inflorescence +of most of our forest trees are merely pendant spikes. The +<em>corymb</em> is a modification +of the raceme in which +the lower pedicels are +elongated so as to place +their flowers on a level +with those of the upper +nodes, making a convex, +or more or less flat-topped +cluster, as in the +wallflower and hawthorn. +The <em>umbel</em> differs +from the corymb in +having the pedicels with +their bracts all gathered +at the top of the peduncle,<span class="pagenum" id="Page_143">[Pg 143]</span> +from which they spread in every direction like the +rays of an umbrella, as the name implies. This is the prevalent +type of flower cluster in the parsley family, which takes +its botanical name, <i>Umbelliferæ</i>, from +its characteristic +form of inflorescence. +The pedicels +of an umbel +are called <em>rays</em>, and +the circle of bracts +at the base of the +cluster is an <em>involucre</em>.</p> + +<table class='autotable'> +<tr> +<td class='wd50'> +<figure class="figcenter illowp60" id="i_153" style="max-width: 20em;"> + <img class="w100" src="images/i_153.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 169.</span>—Corymb +of plum blossoms.</p></figcaption> +</figure> +</td><td class='wd50'> +<figure class="figcenter illowp60" id="i_153a" style="max-width: 20em;"> + <img class="w100" src="images/i_153a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 170.</span>—Umbel of milkweed.</p></figcaption> +</figure> +</td> +</tr><tr> +<td> +<figure class="figcenter illowp60" id="i_153b" style="max-width: 18em;"> + <img class="w100" src="images/i_153b.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 171.</span>—Panicle +of grass, a compound +cluster of the racemose +type.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_153c" style="max-width: 20em;"> + <img class="w100" src="images/i_153c.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 172.</span>—Flat-topped +cyme of sneezeweed.</p></figcaption> +</figure></td></tr></table> + +<p id="p-162"><b>162. Determinate, +or cymose, +inflorescence.</b>—In the <em>cyme</em>, the typical cluster of the determinate +kind, the older blossoms in the center, being terminal, +stop the axis of growth in that direction and force the +stem, in continuing its growth, to send out side branches +from the axils of the topmost leaves, in +a manner precisely +similar to the two-forked +branching of +stems like the horse-chestnut +and jimson +weed. When the older +peduncles are lengthened +as described in +<a href="#p-161">161</a>, a flat-topped cyme +is produced, which is +distinguished from the +corymb by its order of +flowering, the oldest +blossoms being at the +center, while in the corymb they appear in the reverse +order. A peculiar form of cyme is found in the scorpioid<span class="pagenum" id="Page_144">[Pg 144]</span> +or coiled inflorescence of the pink-root (<i>Spigelia</i>), heliotrope, +comfrey, etc. Its structure will be made clear by an inspection +of <a href="#i_154a">Figs. 174-176</a>.</p> + +<figure class="figcenter illowp60" id="i_154" style="max-width: 50em;"> + <img class="w100" src="images/i_154.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Fig. 173.</span>—Scorpioid cyme.</p></figcaption> +</figure> + +<p id="p-163"><b>163. The nature of flower stems.</b>—A comparison of +the types of inflorescence with the modes of branching in +ordinary stems (<a href="#p-144">144</a>, <a href="#p-152">152</a>, <a href="#p-153">153</a>) will show a strict correspondence +between them. Both bear leaves and buds, and +the individual flowers of a cluster usually spring from the<span class="pagenum" id="Page_145">[Pg 145]</span> +axils of leaves or from bracts, which are merely reduced +leaves. What, then, is the essential nature of flower stems?</p> + +<figure class="figcenter illowp80" id="i_154a" style="max-width: 50em;"> + <img class="w100" src="images/i_154a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 174-176.</span>—Diagrams of cymose inflorescence, with flowers numbered in the +order of their development: 174, cyme half developed (scorpioid); 175, a flat-topped +or corymbose cyme; 176, development of a typical cyme.</p></figcaption> +</figure> + +<p id="p-164"><b>164. Significance of the clustered arrangement.</b>—As a +general thing the clustered arrangement marks a higher stage +of development than the solitary, just as in human life the +rudest social state is a distinct advance upon the isolated +condition of the savage. In plant life it is the beginning of +a system of coöperation and division of labor among the associated +members of the flower cluster, as will be seen later +when we take up the study of the flower.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Name as many solitary flowers as you can think of.</p> + +<p>2. Do you, as a rule, find very small flowers solitary, or in clusters?</p> + +<p>3. Would the separate flowers of the clover, parsley, or grape be readily +distinguished by the eye among a mass of foliage?</p> + +<p>4. Should you judge from these facts that it is, in general, advantageous +to plants for their flowers to be conspicuous?</p> +</div> + + +<h4 id="CH_V_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>(1) In connection with <a href="#p-144">144-154</a>, the characteristic modes of branching +among the common trees and shrubs of each neighborhood should be +observed and accounted for. The naked branches of the winter woods +afford exceptional opportunities for studies of this kind, which cannot +well be carried on except out of doors. Note the effect of the mode of +branching upon the general outline of the tree; compare the direction and +mode of growth of the larger boughs with that of small twigs in the same +species, and see if there is any general correspondence between them; note +the absence of fine spray on the boughs of large-leaved trees, and account +for it. Account for the flat sprays of trees like the elm, beech, hackberry, +etc.; the irregular stumpy branches of the oak and walnut; the stiff +straight twigs of the ash; the zigzag switches of the black locust, Osage +orange, elm, and linden. Measure the twigs on various species, and see +if there is any relation between the length and thickness of branches. +Notice the different trend of the upper, middle, and lower boughs in most +trees, and account for it. Observe the mode of branching of as many +different species as possible of some of the great botanical groups of trees; +the oaks, hickories, hawthorns, and pines, for instance, and notice whether +it is, as a general thing, uniform among the species of the same group, and +how it differs from that of other groups.</p> + +<p><span class="pagenum" id="Page_146">[Pg 146]</span></p> + +<p>(2) In connection with <a href="#p-155">155-158</a>, buds of as many different kinds as +possible should be examined with reference to their means of protection, +their vernation and leaf arrangement, and the resulting modes of growth. +Compare the folding of the cotyledons in the seed with the vernation of +the same plants, and observe whether the folding is the same throughout +a whole group of related plants, or only for the same species. Notice which +modes seem to be most prevalent. Select a twig on some tree near your +home or your schoolhouse, and keep a record of its daily growth from the +first sign of the unfolding of its principal bud to the full development of +its leaves. Any study of buds should include an observation of them in +all stages of development.</p> + +<p>(3) With <a href="#p-160">160-165</a>, study the inflorescence of the common plants and +weeds that happen to be in season, until you have no difficulty in distinguishing +between the definite and indefinite sorts, and can refer any +ordinary cluster to its proper form. Notice whether there is any tendency +to uniformity in the mode of inflorescence among flowers of the same family. +Consider how each kind is adapted to the shape and habit of the +flowers composing it, and what particular advantage each of the specimens +examined derives from the way its flowers are clustered. In cases of mixed +inflorescence, see if you can discover any reason for the change from one +form to the other.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_147">[Pg 147]</span></p> + +<h2 class="nobreak" id="CH_VI">CHAPTER VI. THE LEAF</h2> +</div> + + +<h3 id="CH_VI_I">I. THE TYPICAL LEAF AND ITS PARTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Leaves of different kinds showing the various modes of +attachment, shapes, texture, etc. For stipules, leaves on very young +twigs should be selected, as these bodies often fall away soon after the +leaves expand. The rose, Japan quince, willow, strawberry, pea, pansy, +and young leaves of beech, apple, elm, tulip tree, India rubber tree, +magnolia, knotweed, furnish good examples of stipules. For the different +orders of leaf arrangement, lilac, maple, spurge, trillium, cleavers (Galium) +show the opposite and whorled kinds. Elm, basswood, grasses; alder, +birch, sedges; peach, apple, cherry, show respectively for each group the +three principal orders of alternate arrangement.</p> +</div> + +<p id="p-165"><b>165. Parts of the leaf.</b>—Examine a young, healthy leaf +of apple, quince, or elm, as it stands upon the stem, and +notice that it consists of three parts: a +broad expansion called the <em>blade</em>; a leaf +stalk or <em>petiole</em> that attaches it to the +stem; and two little leaflike or bristle-like +bodies at the base, known +as <em>stipules</em>. Make a +sketch of any leaf provided +with all these parts, +and label them, respectively, +blade, petiole, and +stipules. These three parts make up a perfect +or typical leaf, but as a matter of fact, +one or more of them is usually wanting.</p> + +<table class='autotable'> +<tr> +<td> +<figure class="figcenter illowp70" id="i_157" style="max-width: 15.75em;"> + <img class="w100" src="images/i_157.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 177.</span>—A typical +leaf and its parts: +<i>b</i>, blade; <i>p</i>, petiole; +<i>s</i>, <i>s</i>, stipules.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_157a" style="max-width: 12.5em;"> + <img class="w100" src="images/i_157a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 178.</span>—Spiny +stipules of clotbur.</p></figcaption> +</figure></td></tr></table> + +<p id="p-166"><b>166. Stipules.</b>—The office of stipules, +when present, is generally to subserve in +some way the purposes of protection. In many cases, as in +the fig, elm, beech, oak, magnolia, etc., they appear only as +protective scales that cover the bud during winter, and fall<span class="pagenum" id="Page_148">[Pg 148]</span> +away as soon as the leaf expands. When <em>persistent</em>, that is, +enduring, they take various forms according to the purposes +they serve. But under whatever guise they occur, their +true nature may be recognized by their position on each side +of the base of the petiole, and not in the <em>axil</em>, or angle formed +by the leaf with the stem. (<a href="#p-149">149</a>.)</p> + +<table class='autotable'> +<tr> +<td class='vat'> +<figure class="figcenter illowp70" id="i_158a" style="max-width: 31.5625em;"> + <img class="w100" src="images/i_158a.jpg" alt=""> + <figcaption> + <span class="smcap">Fig. 179.</span>—Adnate + stipules of clover. + </figcaption> +</figure> +</td><td class='vat'> +<figure class="figcenter illowp70" id="i_158b" style="max-width: 30.25em;"> + <img class="w100" src="images/i_158b.jpg" alt=""> + <figcaption> + <span class="smcap">Fig. 180.</span>—Leaves of smilax, showing stipular tendrils. + </figcaption> +</figure> +</td><td class='wd33 vat'> +<figure class="figcenter illowp70" id="i_158c" style="max-width: 25.125em;"> + <img class="w100" src="images/i_158c.jpg" alt=""> + <figcaption> + <span class="smcap">Fig. 181.</span>—Leafy stipules of Japan quince. + </figcaption> +</figure></td></tr></table> + + +<p id="p-167" class='cb'><b>167. Leaf attachment.</b>—The normal use of the petiole is +to secure a better light exposure for the leaves, but, like other +parts, it is subject to modifications, and is often wanting +altogether. In this case the leaf is said to be <em>sessile</em>, that is, +<em>seated</em>, on the stem, and the leaf bases are designated by +various terms descriptive of their mode of attachment. The +meaning of these terms, when not self-explanatory, can best +be learned by a comparison of living specimens with <a href="#i_159">Figs. +184-187</a>.</p> + +<p id="p-168"><b>168. Arrangement of leaves on the stem.</b>—The mode +of attachment is something quite distinct from the mode of +leaf arrangement on the stem, or <em>phyllotaxy</em>, as it is termed +by botanists. It was seen in <a href="#p-148">148</a> that this takes place in two +different ways, the alternate and opposite. These two kinds +of arrangement represent the principal forms of leaf disposition<span class="pagenum" id="Page_149">[Pg 149]</span> +on the stem, the different varieties of each depending on +the manner in which the leaves are distributed.</p> + +<figure class="figcenter illowp70" id="i_159" style="max-width: 99.7em;"> + <img class="w100" src="images/i_159.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 182-187.</span>—Petioles, and leaf attachment: 182, petioles of jasmine nightshade +(<i>Solanum jasminoides</i>) acting as tendrils; 183, acacia, showing petiole +transformed to leaf blade; 184, sessile leaves of epilobium; 185, clasping leaf of +lactuca; 186, perfoliate leaves of uvularia; 187, peltate leaf of tropæolum. (182 and +186 <i>after</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p>Where three or more occur at a node, as in the trillium +and cleavers (<i>Galium</i>), they constitute a whorl, which is only +a variant of the opposite arrangement. There is no limit to +the number of leaves that may be in a whorl except the space +around the stem to accommodate them.</p> + +<p>The phyllotaxy of alternate leaves is more complicated.<span class="pagenum" id="Page_150">[Pg 150]</span> +The different forms are characterized by +the angular distance between the points +of leaf insertion around the stem. In the +elm, basswood, and most grasses, they are +distributed in two rows or ranks on opposite +sides of the stem, each just half +way round the circumference from the +one next in succession (<a href="#i_160a">Fig. 189</a>), the +third in vertical order standing directly +over the first. In most of our common +trees and shrubs five leaves are passed +in making two turns round the stem, +the sixth leaf in vertical order standing +over the first. This is called the five-ranked arrangement, +and is the most +common order among +dicotyls.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp55" id="i_160" style="max-width: 29.5em;"> + <img class="w100" src="images/i_160.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 188.</span>—Whorled +leaves of Indian cucumber.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp55" id="i_160a" style="max-width: 60.8em;"> + <img class="w100" src="images/i_160a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 189.</span>—Twig of a hackberry (<i>Celtis cinerea</i>), +showing the two-ranked arrangement. Notice how +the position of the stems and branches of the main +axis corresponds to that of the leaves.</p></figcaption> +</figure></td></tr></table> + +<p id="p-169"><b>169. Relation between +the shape and +arrangement of leaves.</b>—Phyllotaxy +is of importance +chiefly on account +of its influence +on the light relation of +leaves. A compact, +close-ranked arrangement +tends to shut off +the light from the lower +nodes, and hence, in +plants where it prevails, +the leaves are apt +to be long and narrow +in proportion to the +frequency of the vertical +rows. The yucca, +oleander, Canada fleabane +and bitterweed (<i>Helenium +tenuifolium</i>), illustrate this relation.</p> + +<p><span class="pagenum" id="Page_151">[Pg 151]</span></p> + +<figure class="figcenter illowp75" id="i_161" style="max-width: 50em;"> + <img class="w100" src="images/i_161.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 9.</span>—Vegetation of a moist, shady ravine. Notice the expanded surface of +the leaf blades and the long internodes that separate the individual leaves. (From +Rep’t. Mo. Botanical Garden.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_152">[Pg 152]</span></p> + +<figure class="figright illowp30" id="i_162" style="max-width: 24.625em;"> + <img class="w100" src="images/i_162.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 190.</span>—Narrow leaves +in crowded vertical rows.</p></figcaption> +</figure> + +<p>On the other hand, when the leaves +are large and rounded in outline, as +those of the sunflower, hollyhock, and +catalpa, they are usually separated +by longer internodes, or their blades +are cut and incised so that the sunlight +easily strikes through to the +lower ones.</p> + +<p id="p-170"><b>170. Other external characteristics</b> +to be observed in leaves are:—</p> + +<p>(1) General Outline: whether round, oval, heart-shaped, +etc. (<a href="#i_162a">Figs. 191-197</a>).</p> + +<p>(2) Margins: whether unbroken (<em>entire</em>), or variously +toothed and indented. (<a href="#i_163">Figs. 198-202</a>.)</p> + +<p>(3) Texture: whether thick, thin, soft, hard, fleshy, +leathery, brittle.</p> + +<p>(4) Surface: smooth, shining, dull, wrinkled, hairy, or +otherwise roughened.</p> + +<figure class="figcenter illowp75" id="i_162a" style="max-width: 50em;"> + <img class="w100" src="images/i_162a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 191-197.</span>—Shapes of leaves: 191, lanceolate; 192, spatulate; 193, oval; +194, obovate; 195, kidney-shaped; 196, deltoid; 197, lyrate. (191-195 <i>after</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_153">[Pg 153]</span></p> + +<p>Not only do leaves of different +kinds exhibit these characteristics +in varying degrees, but young and +old leaves, or those on young and +old plants of the same kind, often +differ from each other in color, size, +shape, texture, mode of attachment, +and the like, to such a degree (<a href="#i_163a">Figs. +203, 204</a>) that one not familiar +with them in both stages would +hardly recognize them as belonging to the same species. +The young leaves +of eucalyptus, mulberry, +and some oaks +afford conspicuous +examples of such +differences, and they +exist between the +cotyledons and mature +leaves of most +plants.</p> + +<p>Can you see any +benefit, in the case +of the plant whose +leaves you are studying, +that could be +derived from such of +the characteristics +named above as +they may exhibit?</p> + +<table class='autotable'> +<tr><td class='tdc wd50'> +<figure class="figcenter illowp60" id="i_163" style="max-width: 21.75em;"> + <img class="w100" src="images/i_163.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 198-202.</span>—Margins of +leaves: 198, serrate; 199, dentate; +200, crenate; 201, undulate; +202, sinuate. (<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> +</td><td class='tdc wd50'> +<figure class="figcenter illowp60" id="i_163a" style="max-width: 54.75em;"> + <img class="w100" src="images/i_163a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 203, 204.</span>—Leaves of paper mulberry tree: +203, leaf from an old tree; 204, leaf from a two-year-old +sprout.</p></figcaption> +</figure></td></tr></table> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Tell the nature and use of the stipules in such of the following plants +as you can find: tulip tree; fig; beech; apple; willow; pansy; garden +pea; Japan quince (<i>Pyrus Japonica</i>); sycamore; rose; paper mulberry +(<i>Broussonetia</i>).</p> + +<p><span class="pagenum" id="Page_154">[Pg 154]</span></p> + +<p>2. How would you distinguish between a chinquapin, a chestnut, a +chestnut oak, and a horse-chestnut tree by their leaves alone? By their +bark and branches? Between a hickory, ash, common elder, box elder, +ailanthus, sumach? Between beech, birch, elm, hackberry, alder?</p> + +<p>(Any other sets of leaves may be substituted for those named, the object +being merely to form the habit of distinguishing readily the differences +and resemblances among those that bear some general likeness to one +another.)</p> + +<p>3. From the study of these or similar specimens, would you conclude +that resemblances in leaves are confined to those of closely related kinds?</p> + +<p>4. Name some causes independent of botanical relationship that might +influence them. (<a href="#p-169">169</a>, <a href="#p-170">170</a>; <a href="#exp-48">Exps. 48</a>, <a href="#exp-57">57</a>.)</p> + +<p>5. Do you find, as a general thing, more leaves with stipules or without?</p> + +<p>6. Is their absence from a mature leaf always a sign that it is really +exstipulate? (<a href="#p-166">166</a>.)</p> + +<p>7. Can you trace any line of development through intervening forms +from a merely sessile leaf, like that of the pimpernel or specularia, to a +peltate one? (<a href="#i_159">Figs. 184-187</a>, and observation of living specimens.)</p> + +<p>8. Does the leaf determine the position of the node, or the node the +position of the leaf?</p> + +<p>9. Strip the leaves from a twig of one order of arrangement and replace +them with foliage from a twig of a different order; for instance, place +basswood upon white oak, birch upon lilac, elm upon pear, honeysuckle +upon barberry, etc. Is the same amount of surface exposed as in the +natural order?</p> + +<p>10. What disadvantage would it be to a plant if the leaves were arranged +so that they stood directly over one another? (<a href="#p-169">169</a>.)</p> + +<p>11. Why are the internodes of vigorous young shoots, or scions, generally +so long? (<a href="#p-150">150</a>.)</p> + +<p>12. If the upward growth of a stem or branch is stopped by pruning, +what effect is produced upon the parts below, and why? (<a href="#p-152">152</a>, <a href="#p-153">153</a>.)</p> + +<p>13. Give some of the reasons why corn grows so small and stunted when +sown broadcast for forage? (<a href="#p-60">60</a>, <a href="#p-63">63</a>, <a href="#p-169">169</a>.)</p> + +<p>14. What is the use of “chopping” (<i>i.e.</i> thinning out) cotton?</p> +</div> + + +<h3 id="CH_VI_II">II. THE VEINING AND LOBING OF LEAVES</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Leaves of any monocotyl and dicotyl will show the difference +between parallel and net-veining. To illustrate the palmate and +pinnate kinds, the leaves of grasses and arums may be used for monocotyls, +and for dicotyls, those of ivy, maple, grape, elm, peach, cherry, etc.; for +division, examine lobed and compound leaves of as many kinds as are +attainable. A specimen showing each kind of veining should be placed in<span class="pagenum" id="Page_155">[Pg 155]</span> +coloring fluid a short time before the lesson begins. The leafstalks of +celery and plantain are excellent for showing the relation between the leaf +veins and vascular system of the plant.</p> +</div> + +<p id="p-171"><b>171. Parallel and net veining.</b>—Compare a leaf of the +wandering Jew, lily, or any kind of grass, with one of grape, +ivy, or willow. Hold each up to the light, +and note the veins or little threads of woody +substance that run through it. Make a drawing +of each so as to show plainly the direction +and manner of veining. Write under the +first, <em>parallel-veined</em>, and under the second, +<em>net-veined</em>. This distinction of leaves into +parallel and net-veined corresponds +with the two great +classes into which seed-bearing +plants are divided, monocotyls, +as a general thing, +being characterized by the +first kind, and dicotyls by +the second.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp60" id="i_165" style="max-width: 17.25em;"> + <img class="w100" src="images/i_165.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 205.</span>—Parallel-veined +leaf of +lily of the valley +(<i>After</i> <span class="smcap">Gray</span>).</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_165a" style="max-width: 17.75em;"> + <img class="w100" src="images/i_165a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 206.</span>—Net-veined +leaf of a willow.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_165b" style="max-width: 16.75em;"> + <img class="w100" src="images/i_165b.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 207.</span>—Pinnately +parallel-veined +leaf of calla +lily (<i>After</i> <span class="smcap">Gray</span>).</p></figcaption> +</figure></td></tr></table> + +<figure class="figright illowp30" id="i_166" style="max-width: 27.75em;"> + <img class="w100" src="images/i_166.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 208.</span>—Palmately net-veined +leaf of wild ginger.</p></figcaption> +</figure> + + +<p id="p-172"><b>172. Pinnate and palmate veining.</b>—Next, +compare a leaf of the canna, calla lily, +or any kind of arum, with one of the elm, +peach, cherry, etc. What resemblances do +you notice between the two? What differences? +Which is parallel-veined and which +is net-veined? Make a drawing of each, and +compare with the first two. Notice that in +leaves of this kind, the petiole is continued +in a large central vein, called the <em>midrib</em>, +from which the secondary veins branch off +on either side like the pinnæ of a feather; +whence such leaves are said to be <em>pinnately</em>, +or <em>feather</em> veined, as in <a href="#i_165a">Figs. 206</a>, <a href="#i_165b">207</a>. In +the cotton, maple, ivy, etc., on the other +hand, the petiole breaks up at the base of the<span class="pagenum" id="Page_156">[Pg 156]</span> +leaf (<a href="#i_166">Fig. 208</a>) into a number of primary veins or ribs, which +radiate in all directions like the fingers from the palm of the +hand; hence, such a leaf is said to be <em>palmately</em> veined. +Net-veined leaves—the plantain +(<a href="#i_166a">Fig. 209</a>), wild smilax, beech, dogwood—are +sometimes ribbed in a +way that might lead an inexperienced +observer to confound them +with parallel-veined ones, but the +reticulations between the ribs show +that they belong to the net-veined +class.</p> + +<figure class="figright illowp20" id="i_166a" style="max-width: 20em;"> + <img class="w100" src="images/i_166a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 209.</span>—Ribbed +leaf of plantain.</p></figcaption> +</figure> + +<p id="p-173"><b>173. Veins as a mechanical support.</b>—Hold +up a stiff, firm leaf of any kind, like the magnolia, +holly, or India rubber, to the light, having first scraped +away a little of the under surface, and examine it with a lens. +Compare it with one of softer texture, like +the peach, maple, or clover. In which are +the veins the closer and stronger? Which +is the more easily torn and wilted? Tear a +blade of grass longitudinally and then cross-wise; +in which direction does it give way +the more readily? Tear apart gently a leaf +of maple, or ivy, and one of elm or other +pinnately veined plant; in which direction +does each give way with least resistance? +What would you judge from these facts as +to the mechanical use of the veins?</p> + +<p id="p-174"><b>174. Effect upon shape.</b>—By comparing +a number of leaves of each kind it will be seen that the +feather-veined ones tend to assume elongated outlines (<a href="#i_162a">Figs. +197</a>, <a href="#i_165b">207</a>); the palmate-veined ones, broad and rounded forms +(<a href="#i_162a">Figs. 195</a>, <a href="#i_166">208</a>). Notice also that the straight, unbroken +venation of parallel-veined leaves is generally accompanied by +smooth, unbroken margins, while the irregular, open meshes +of net-veined leaves are favorable to breaks and indentations.</p> + +<p><span class="pagenum" id="Page_157">[Pg 157]</span></p> + +<p id="p-175"><b>175. Veins as water carriers.</b>—Examine a leaf from a +stem that has stood in red ink for an hour or two. Do you +see evidence that it has absorbed any of the liquid? Cut +across the blade and examine with a lens. What course has +the absorbed liquid followed? What use does this indicate +for the veins, besides the one already noted? Observe the +point of insertion on the stem, and examine the scar with a +lens: do you see any evidence of a connection between the +leaf veins and the fibrovascular bundles of the stem? (<a href="#p-111">111</a>, +<a href="#p-125">125</a>, <a href="#p-126">126</a>.) Notice where and how the veins end. Are they +of the same size all the way, or do they grow smaller toward +the tip? Are they separate and distinct, or are they connected +throughout their ramifications, like the veins and +arteries of the human body? How do you know? Do you +see any of the coloring fluid in the small reticulations between +the veins? How did it get there?</p> + +<p id="p-176"><b>176. The nature and office of veins.</b>—We learn from <a href="#p-173">173</a> +and <a href="#p-175">175</a> that the veining serves two important purposes in the +economy of the leaf: first, as a skeleton or framework, to support +the expanded blade; and second, as a system of water +pipes, for conveying the sap out of which its food is manufactured. +In other words the veins are a continuation of the +fibrovascular bundles into the leaves, by means of which the +latter are put in communication with the body of the plant.</p> + +<p id="p-177"><b>177. The relation between veining and lobing.</b>—Compare +the outline of a leaf of maple or ivy with one of oak or +chrysanthemum. Do you perceive any correspondence between +the manner of lobing or indentation of their margins, +and the direction of the veins? (<a href="#i_168_210">Figs. 210</a>, <a href="#i_168_211">211</a>.) To what +class would you refer each one?</p> + +<p>The lobes themselves may be variously cut, as in the +fennel and rose geranium, thus giving rise to twice-cleft, +thrice-cleft (<a href="#i_168_212">Fig. 212</a>), four-cleft, or even still more intricately +divided blades.</p> + +<p id="p-178"><b>178. Compound leaves.</b>—Compare with the specimens +just examined a leaf of horse-chestnut, clover, or Virginia +creeper, and one of rose, black locust, or vetch. Notice that +each of these last is made up of entirely separate divisions or +leaflets, thus forming a <em>compound leaf</em>. Notice also that the +two kinds of compound leaves correspond to the two kinds of +veining and lobing, so that we have palmately and pinnately +compound ones. In pinnate leaves the continuation of the +common petiole along which the leaflets are ranged is called +the <em>rhachis</em>.</p> + +<p><span class="pagenum" id="Page_158">[Pg 158]</span></p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp50" id="i_168_210" style="max-width: 21.3125em;"> + <img class="w100" src="images/i_168_210.jpg" alt="" data-role="presentation"> + <figcaption><p> + <span class="smcap">Fig. 210.</span>—Pinnately + lobed leaf of horse nettle.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp56" id="i_168_211" style="max-width: 18.1875em;"> + <img class="w100" src="images/i_168_211.jpg" alt="" data-role="presentation"> + <figcaption><p> + <span class="smcap">Fig. 211.</span>—Palmately + lobed leaf of grape.</p> + </figcaption> +</figure></td></tr></table> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp70" id="i_168_212" style="max-width: 44.4375em;"> + <img class="w100" src="images/i_168_212.jpg" alt="" data-role="presentation"> + <figcaption><p> + <span class="smcap">Fig. 212.</span>—Palmately parted leaf of a buttercup. + </p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp70" id="i_168_213" style="max-width: 25.5em;"> + <img class="w100" src="images/i_168_213.jpg" alt="" data-role="presentation"> + <figcaption><p> + <span class="smcap">Fig. 213.</span>—Pinnately compound leaf of black locust. + </p></figcaption> +</figure></td></tr></table> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp70" id="i_168_214" style="max-width: 37.0625em;"> + <img class="w100" src="images/i_168_214.jpg" alt=""> + <figcaption><p> + <span class="smcap">Fig. 214.</span>—Palmately compound leaf of horse-chestnut.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp70" id="i_168_215" style="max-width: 26.6875em;"> + <img class="w100" src="images/i_168_215.jpg" alt=""> + <figcaption><p> + <span class="smcap">Fig. 215.</span>—Pinnately trifoliolate leaf of a desmodium.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp70" id="i_168_216" style="max-width: 26.5em;"> + <img class="w100" src="images/i_168_216.jpg" alt=""> + <figcaption><p> + <span class="smcap">Fig. 216.</span>—Palmately trifoliolate leaf of wood sorrel.</p> + </figcaption> +</figure></td></tr></table> + + +<p><span class="pagenum" id="Page_159">[Pg 159]</span></p> + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. In selecting leaves for decorations that are to remain several hours +without water, which of the following would you prefer, and why: +smilax or Madeira vine (<i>Boussingaultia</i>); ivy or Virginia creeper; +magnolia or maple; maidenhair or shield fern (<i>Aspidium</i>)? (<a href="#p-173">173</a>.)</p> + +<p>2. Would you select very young leaves, or more mature ones, and why?</p> + +<p>3. Can you name any parallel-veined leaves that have their margins +lobed, or indented in any way?</p> + +<p>4. Which are the more common, parallel-veined or net-veined leaves?</p> + +<p>5. Why do the leaves of corn and other grains not shrivel lengthwise in +withering, but roll inward from side to side? (<a href="#p-173">173</a>.)</p> + +<p>6. Can you name any palmately veined leaves in which the secondary +veins are pinnate? Any pinnately veined ones in which the secondary +veins are palmate?</p> + +<p>7. Lay one of each kind before you; try to draw a pinnate leaf with +palmate divisions. Do you see any reason now why these so seldom occur +in nature?</p> + +<p>8. Name some advantages to a plant in having its leaves cut-lobed or +compound. (<a href="#p-169">169</a>.)</p> + +<p>9. Mention some circumstances under which it might be advantageous +for a plant to have large, entire leaves. (<a href="#p-169">169</a>; <a href="#i_161">Plate 9</a>.)</p> + +<p>10. How would the floating qualities of the leaves of the pond lily be +affected if their blades were cut-lobed or compound?</p> + +<p>11. Do the leaves of the red cedar and arbor vitæ contribute to their +value as shade trees?</p> + +<p>12. Name some of the favorite shade trees of your neighborhood; do +they, as a general thing, have their leaves entire, or lobed and compound?</p> + +<p>13. Which of the following are the best shade trees, and why: pine, +white oak, mimosa (<i>Albizzia</i>), sycamore, locust, horse-chestnut, fir, maple, +linden, China tree, cedar, ash?</p> + +<p>14. Which would shade your porch best, and why: cypress vine, +grape, gourd, morning-glory, wistaria, clematis, smilax, kidney bean, +Madeira vine, rose, yellow jasmine, passion flower?</p> +</div> + +<p><span class="pagenum" id="Page_160">[Pg 160]</span></p> + + +<h3 id="CH_VI_III">III. TRANSPIRATION</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Leafy twigs of actively growing young plants. Sunflower, +corn, peach, grape, calla, and arums in general transpire rapidly; +thick-leaved evergreens and hairy or rough species, like mullein and horehound +more slowly. For <a href="#exp-63">Exp. 63</a>, small-leaved, large-leaved, and thick-leaved +kinds will be needed.</p> + +<p><span class="smcap">Appliances.</span>—Glass jars and bottles with air-tight stoppers; a little +vaseline, oil, gardener’s wax, thread, cardboard, and a pair of scales.</p> + +<p id="exp-62"><span class="smcap">Experiment 62. To show why leaves wither.</span>—Dry two self-sealing +jars thoroughly, by holding them over a stove or a lighted lamp +for a short time to prevent “sweating.” Place in one a freshly cut leafy +sprig of any kind, leaving the other empty. Seal both jars and set them +in the shade. Place beside them, but without covering of any kind, a +twig similar to the one in the jar. Both twigs should have been cut at +the same time, and their cut ends covered with wax or vaseline, to prevent +access of air. Look at intervals to see if there is any moisture deposited +on the inside of either jar. If there is none, set them both in a refrigerator +or cover with a wet cloth and allow to cool for half an hour, and then examine +again. In which jar is there a greater deposit of dew? How do you +account for it? Take the twig out of the jar and compare its leaves with +those of the one left outside; which have withered the more, and why?</p> + +<p id="exp-63"><span class="smcap">Experiment 63. To measure the rate at which water is +given off by leaves of different kinds.</span>—Fill three glass vessels of +the same size with water and cover with oil to prevent evaporation. +Insert into one the end of a healthy twig of peach or cherry; into the +second a twig of catalpa, grape, or any large-leaved plant, and into +the third, one of magnolia, holly, or other thick-leaved evergreen, letting +the stems of all reach well down into the water. Care must be taken to +select twigs of approximately the same size and age, since the absorbent +properties of very young stems are more injured by cutting and exposure +than those of older ones. All specimens should be cut under water as +directed in <a href="#exp-58">Exp. 58</a>. Weigh all three vessels, and at the end of twenty-four +hours, weigh again, taking note of the quantity of liquid that has disappeared +from each glass. This will represent approximately the amount +absorbed by the leaves from the twigs to replace that given off. Which +twig has lost most? Which least? Note the condition of the leaves +on the different twigs; have they all absorbed water about as rapidly +as they have lost it? How do you know this? Pluck the leaves from +each twig, one by one, lay them on a flat surface that has been previously +measured off, into square inches or centimeters, and thus form a rough +estimate of the area covered by each specimen. Make the best estimate<span class="pagenum" id="Page_161">[Pg 161]</span> +you can of the number of leaves on each tree, and calculate the number +of kilograms of water it would give off at that rate in a day.</p> + +<p id="exp-64"><span class="smcap">Experiment 64. Through what part of the leaf does the water +get out?</span>—Take some healthy leaves of tulip tree, grape, tropæolum, +or any large, soft kind attainable. Cover with vaseline the <em>leafstalk</em> and +<em>upper</em> surface of one; the stalk and <em>under</em> surface of a second; the stalk +and <em>both</em> surfaces of a third, and leave a fourth one untreated. Suspend +all four in a dry place by means of a thread attached to the petioles so +that both surfaces may be equally exposed. The leaves must be all of +the same species, and as nearly as possible of the same age, size, and vigor, +and care must be taken that none of the vaseline is rubbed off in handling. +Examine at intervals of a few hours. Which of the leaves withers soonest? +Which keeps fresh longest? From what part would you conclude, judging +by this experiment, that the water escapes most rapidly?</p> +</div> + +<p id="p-179"><b>179. Transpiration, nutrition, and growth.</b>—We learn +from the foregoing, and from <a href="#exp-58">Exps. 58</a> and <a href="#exp-59">59</a>, that plants +give off moisture very much as animals do by perspiration. +The two processes must not be classed together, however, +for they are physiologically different. The action, in plants, +is called <em>transpiration</em>. It is usually assumed that a large +amount of water must pass through the plant in order to +bring to it the necessary supply of food material; but since +the entrance of mineral salts is brought about by osmosis, +conditioned by the living cells of the root; and since osmosis +of salts may take place in a direction opposite to that of the +greater movement of water, it follows that the entrance of +salts is independent of transpiration.</p> + +<p>Inasmuch, however, as a certain amount of water is +necessary to bring the living cells into a condition of turgor +(7) so that they may grow, it follows that there is a relation +between transpiration and growth. If transpiration exceeds +absorption for any length of time, the tissues will be depleted +of their moisture, as is shown by the wilting of crops +in dry, hot weather; and if the unequal movement continues +long enough, the plant will die. Hence, a knowledge of the +laws governing this important function is necessary to all +who are interested in cultivating agricultural products.</p> + +<p><span class="pagenum" id="Page_162">[Pg 162]</span></p> + +<figure class="figright illowp50" id="i_172_2" style="max-width: 70.5em;"> + <img class="w100" src="images/i_172.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 217.</span>—A “weeping tree,” showing the effect where + absorption exceeds transpiration. Notice the position of + the tree near the water where the roots have unlimited + moisture. (<i>After</i> <span class="smcap">Francé</span>.)</p> + </figcaption> +</figure> + +<p id="p-180"><b>180. Magnitude of the work of transpiration.</b>—Few +people have any idea of the enormous quantities of water +given off by leaves. It has been calculated that a healthy +oak may have as many as 700,000 leaves, and that 111,225 +kilograms of water—equal to about 244,700 pounds—may +pass from its surface in the five active months from June +to October. At +this rate 226 +times its own +weight may pass +through it in a +year, and it +would transpire +water enough +during that time +to cover the +ground shaded +by it to a depth +of 20 feet!<a id="FNanchor_2" href="#Footnote_2" class="fnanchor">[2]</a> +Lawn grass gives +off water at such +a rate that a vacant +lot of 150 × +50 feet, if well +turfed, would be +capable of transpiring +over a ton +of water a day. Compare these figures with the average yearly +rainfall in our Gulf States—53 inches, approximately—and +you can form some estimate of the injury done to a growing +crop from this cause alone. The moisture is drawn from the +surface by shallow rooted weeds <a href="#p-81">(81)</a> and dissipated through +the leaves. In the case of forest trees the effect is different. +Their roots, striking deep into the soil, draw up water from +the lower strata and distribute it to the thirsty air in summer.</p> + +<p><span class="pagenum" id="Page_163">[Pg 163]</span></p> + +<p>As the water given off by transpiration is in the form of +vapor, it must draw from the plant the amount of heat +necessary for its vaporization, and thus has the effect of +making the leaves and the air in contact with them cooler +than the surrounding medium. At the same time the coolness +and moisture of the air tend to check the loss by +evaporation from the surface soil. It is partly to this cause, +and not alone to their shade, that the coolness of forests is +due. Measurements at various weather bureau stations in +the United States show that in summer the temperature of +oak woods is 4° C. lower during the day than in the open, +and as much higher at night. In a beech wood in Germany +the difference between the forest and the general temperature +amounted to as much as 7° C.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Is there any foundation in fact for the accounts of “weeping trees” +and “rain trees” that we sometimes read about in the papers? (<a href="#p-180">180</a>; +<a href="#exp-48">Exp. 48</a>.)</p> + +<p>2. Can you explain the fact, sometimes noticed by farmers, that in +wooded districts, springs which have failed or run low during a dry spell +sometimes begin to flow again in autumn when the trees drop their leaves, +even though there has been no rain? (<a href="#p-180">180</a>; <a href="#exp-63">Exp. 63</a>.)</p> + +<p>3. Other things being equal, which would have the cooler, pleasanter +atmosphere in summer, a well-wooded region or a treeless one? (<a href="#p-180">180</a>.)</p> + +<p>4. Could you keep a bouquet fresh by giving it plenty of fresh air? +(<a href="#exp-62">Exp. 62</a>.)</p> + +<p>5. Why does a withered leaf become soft and flabby, and a dried one +hard and brittle? (<a href="#p-7">7</a>; <a href="#exp-62">Exp. 62</a>.)</p> + +<p>6. Why do large-leaved plants, as a general thing, wither more quickly +than those with small leaves? (<a href="#exp-63">Exp. 63</a>.)</p> + +<p>7. Is the amount of water absorbed always a correct indication of the +amount transpired? Explain. (<a href="#p-179">179</a>.)</p> + +<p>8. Explain the difference between the withering caused by excessive +transpiration and the shrinkage of cells due to plasmolysis. Are both of +these physiological processes?</p> + +<p>9. Why is it best to trim a tree close when it is transplanted? (<a href="#p-179">179</a>, +<a href="#p-180">180</a>.)</p> + +<p>10. Why should transplanting be done in winter or very early spring, +before the leaves appear? (<a href="#p-180">180</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_164">[Pg 164]</span></p> + + +<h3 id="CH_VI_IV">IV. ANATOMY OF THE LEAF</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For study of the epidermis, leaves of the white garden +lily (<i>Lilium album</i>) are best, as the stomata can be seen on their lower +surface with the naked eye. Wandering Jew, Spanish bayonet (<i>Yucca +aloifolia</i>), anemone, narcissus, iris, canna, show them under a hand lens, +but less distinctly. For sections, beet, mustard, and beech leaves may +be used, or ready-mounted specimens obtained of a dealer.</p> + +<p>A compound microscope is needed for a minute study of the leaf +structure.</p> +</div> + +<figure class="figright illowp30" id="i_174" style="max-width: 17.75em;"> + <img class="w100" src="images/i_174.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 218, 219.</span>—Stomata +of white lily +leaf: 218, closed; 219, +open. (<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-181"><b>181. Stomata.</b>—It was shown in <a href="#exp-64">Exp. 64</a> that the water +of transpiration escapes most rapidly, as a general thing, from +the under surface of leaves. To find out why this is so, a +careful study of the epidermis will be necessary. For this +purpose procure, if possible, the leaf of a white garden lily +(<i>Lilium album</i>), wandering Jew, Spanish bayonet (<i>Yucca +aloifolia</i>), anemone, narcissus, iris, or canna. The first-named +is preferable, as the transpiration +pores can be seen on it with the naked eye. +Examine the under surface with a hand +lens, and you will see that it is covered with +small eye-shaped dots like those shown in +<a href="#i_174">Figs. 218 and 219</a>. Strip off a portion of +the epidermis, hold it up to the light on a +piece of moistened glass, and they can be +seen quite clearly with a lens. These dots +are the pores through which the water vapor escapes in +transpiration, and through which air finds its way into the +tissues of the leaf. They are called <em>stomata</em> (sing., <em>stoma</em>), +from a Greek word meaning “a mouth.” Look for stomata +on the upper epidermis; do you find any, and if so, are there +as many as on the under surface? Do you see any relation +between this fact and the results obtained from <a href="#exp-64">Exp. 64</a>? +Can you see any good reasons why the stomata should be +placed on the under side in preference to the upper? Are they +as much exposed to excessive light and heat, or as liable to +be choked by dust, rain, and dew here as on the upper side?</p> + +<p><span class="pagenum" id="Page_165">[Pg 165]</span></p> + +<p id="p-182"><b>182. Distribution of stomata.</b>—While stomata are generally +more abundant on the under side of leaves, this is not +always the case. In vertical leaves, like those of the iris, +which have both sides equally exposed to the sun, they are +distributed equally on both sides. In plants like the water +lily, where the under surface lies upon the +water, they occur only on the upper side. +Succulent leaves, as a general thing, have +very few, because they need to conserve +all their moisture. Submerged leaves +have none at all; why?</p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp50" id="i_175" style="max-width: 20em;"> + <img class="w100" src="images/i_175.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 220.</span>—A small +piece of the under epidermis +of an oak leaf, highly +magnified to show the +stomata, <i>g</i>, and minute +hairs, <i>h</i>.</p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp50" id="i_175a" style="max-width: 18.5em;"> + <img class="w100" src="images/i_175a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 221.</span>—Under +epidermis of an oat leaf, +showing stomata.</p></figcaption> +</figure></td></tr></table> + +<p id="p-183"><b>183. Minute study of a leaf epidermis.</b>—Place +a bit of the lower epidermis of +a leaf under the microscope, and examine +with a high power. It will appear, if a +monocotyl, to be composed of long, flat, +rectangular spaces (<a href="#i_175a">Fig. 221</a>); if the leaf +of a dicotyl is used, they will be more or less irregular (<a href="#i_175">Fig. +220</a>), with the outlines fitting into each other like the tiling +of a floor or the blocks of a Chinese puzzle. +These spaces are the cells of the epidermis, +and the lines are the cell walls. Can you +find any of the cell contents? The cell +sap is not often visible; do you see the +nuclei? Can you give a reason why the +epidermal cells are so thin and flat? Between +some of the cells you will see two +kidney-shaped bodies placed with their +concave sides together so as to leave a +lenticular opening between them. This +is a <em>stoma</em>, and the kidney-shaped bodies +(<a href="#i_174">Figs. 218, 219</a>) are <em>guard cells</em>. They +are given this name because they open +or close the mouth of the stoma. If +you will imagine a toy balloon made in the form of a hollow +ring, like the tire of a bicycle, you can easily see, from<span class="pagenum" id="Page_166">[Pg 166]</span> +<a href="#i_174">Figs. 218, 219</a>, that when the ring is strongly inflated, it +will expand, and in enlarging its own circumference, will at +the same time increase the diameter of the opening in the +center. When the expansive +force is removed, +it collapses, thus closing, +or greatly reducing, the +aperture.</p> + +<figure class="figleft illowp50" id="i_176" style="max-width: 39.6875em;"> + <img class="w100" src="images/i_176.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 222.</span>—Outline of a stoma of hellebore +in vertical section. The darker lines show the +shape assumed by the guard cells when the stoma +is open; the lighter lines, when the stoma is +closed. The cavities of the guard cells with the +stoma closed are shaded, and are distinctly +smaller than when the stoma is open.</p></figcaption> +</figure> + +<p>In the same way the +guard cells, when there +is abundance of water in +them, expand, thus opening +the stoma so that the +water vapor passes out +more readily. But when +there is a dearth of +moisture, or when, by reason of chemical action in the soil, +the roots fail to supply it, the leaves wilt, the guard cells, +losing their water, collapse, closing the pore, and transpiration +is thus prevented or greatly retarded. (<a href="#i_176">Fig. 222</a>.)</p> + +<p>Sketch a portion of the epidermis as it appears under the microscope, +labeling the parts. If stomata can be found in both +conditions, make sketches showing them both open and closed.</p> + +<p id="p-184"><b>184. Internal structure of a leaf.</b>—Roll a leaf blade, or +fold it tightly to facilitate cutting, and with a scalpel, or a very +sharp razor, cut the thinnest possible slice through the roll. +This will give a section at right angles to the epidermis. +It should be so thin as to appear almost transparent. Put a +small bit of a section in a drop of water on a slide, place under +the microscope, using a high power, and look for the parts +shown in <a href="#i_177">Fig. 223</a>. Notice the horizontally flattened cells of the +upper epidermis, <i>e</i>, and of the lower epidermis, <i>e′</i>; also the vertically +elongated palisade cells, <i>p</i>, filled with particles of green +coloring matter. These particles are the chlorophyll bodies, +to which the green color of the leaf is due. They are the +active agents in the manufacture of plant food, and in a leaf<span class="pagenum" id="Page_167">[Pg 167]</span> +removed from the plant during the day time and viewed +under a high power, the chlorophyll bodies, on treatment +with iodine, will be seen to contain granules of starch which +they are in the act of elaborating. The collecting cells, <i>t</i>, +receive the assimilated product from the +palisade cells and pass it on through the +spongy parenchyma, <i>sch</i>, to the fibrovascular +bundles. Notice how much more abundant +the green matter is in the upper part of the +leaf than in the lower; has this anything to +do with the deeper color of the upper surfaces +of leaves? Notice the opening, <i>st</i>, +lower epidermis; do you recognize it? (See +<a href="#i_176">Fig. 222</a>.) It is a stoma, seen in vertical +section. Notice the intercellular air spaces, +<i>i</i>, <i>i</i>, in the spongy parenchyma, and the much larger one, <i>a</i>, +just behind the stoma. Why is this last so much larger?</p> + +<figure class="figcenter illowp85" id="i_177" style="max-width: 50em;"> + <img class="w100" src="images/i_177.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 223.</span>—Transverse section through a leaf of beet: <i>e</i>, upper epidermis; <i>e′</i>, +lower epidermis; <i>st</i>, stoma; <i>a</i>, air space; <i>p</i>, palisade cells; <i>t</i>, collecting cells; <i>sch</i>, +spongy parenchyma; <i>i</i>, <i>i</i>, intercellular air spaces; <i>Fbv</i>, section of a vein (fibrovascular +bundle).</p></figcaption> +</figure> + +<figure class="figright illowp20" id="i_177a" style="max-width: 12.5em;"> + <img class="w100" src="images/i_177a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 224.</span>—Chlorophyll +bodies containing +starch grains +in the course of formation. +Magnified +250 times.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_168">[Pg 168]</span></p> + +<p>Sketch the section of your specimen as it appears under +the microscope. It will perhaps differ in some details from +the one shown in the figure, but you can recognize and label +the corresponding parts. Be sure that your drawing represents +accurately the relative size and shapes of the different +kinds of cells.</p> + +<p>It is in the upper surface, where the chlorophyll particles +abound, that the manufacture of food goes on most actively, +and from the under surface, where the stomata are situated, +that transpiration takes place and air and other gases pass +to and from the interior. These facts have important bearings +on the growth and external characters of leaves.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Explain why a plant cannot thrive if its stomata are clogged with +foreign matter. (<a href="#p-179">179</a>; <a href="#exp-64">Exp. 64</a>; <a href="#p-184">184</a>.)</p> + +<p>2. Mention some of the ways in which this might happen. (<a href="#p-181">181</a>.)</p> + +<p>3. Why must the leaves of house plants be washed occasionally to keep +them healthy? (<a href="#p-179">179</a>, <a href="#p-181">181</a>.)</p> + +<p>4. Why is it so hard for trees and hedges to remain healthy in a large +manufacturing town?</p> +</div> + + +<h3 id="CH_VI_V">V. FOOD MAKING</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A sprig of pondweed, mare’s-tail (<i>Hippuris</i>), hornwort +(<i>Ceratophyllum</i>), marsh St.-John’s-wort (<i>Elodea</i>), or other green aquatic +plant; bean or tropæolum, or other green leaves gathered from plants +growing in the sunshine; a healthy potted plant; a small, fresh cutting.</p> + +<p><span class="smcap">Appliances.</span>—A shallow dish of water and two glass tumblers or wide-mouthed +jars; a bent glass or rubber tube; a piece of black cloth or paper; +a half pint of alcohol; iodine solution; a glass funnel or a long-necked +bottle from which the bottom has been removed.</p> + +<p id="exp-65"><span class="smcap">Experiment 65. Is there any relation between sunlight +and the green color of leaves?</span>—Place a seedling of oats, or other +rapidly growing shoot, in the dark for a few days, and note its loss of +color. Leave it in the dark indefinitely, and it will lose all color and die. +Hence we may conclude that there is some intimate connection between +the action of light and the green coloring matter of leaves.</p> + +<p id="exp-66"><span class="smcap">Experiment 66. Do leaves give off anything else besides +water?</span>—Submerge a green water plant, with the cut end uppermost, in<span class="pagenum" id="Page_169">[Pg 169]</span> +a glass vessel full of water, and invert over it a glass funnel, or a long-necked +bottle from which the bottom has been removed as directed in <a href="#exp-53">Exp. +53</a>. Expel the air from the neck of the funnel—or +bottle—by submerging and corking under water +so as to make it air-tight. Place in the sunlight and +notice the bubbles that begin to rise from the cut +end of the plant. When they have partly filled the +neck of the funnel, remove the stopper and thrust +in a glowing splinter. If it bursts into flame, or +glows more brightly, what is the gas that was given +off? (<a href="#exp-22">Exp. 22</a>.)</p> + +<p>As oxygen is not a product of respiration, some +other process must be at work here, during which +oxygen is set free, and some other substance used +up. (Exps. 24 and 25.)</p> + +<table> +<tr><td> +<figure class="figcenter illowp50" id="i_179a" style="max-width: 15.5em;"> + <img class="w100" src="images/i_179a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 225.</span>—Experiment +showing that +green plants give off +oxygen in sunlight.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp50" id="i_179" style="max-width: 25em;"> + <img class="w100" src="images/i_179.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 226.</span>—Experiment +for showing that leaves absorb +carbon dioxide from the atmosphere.</p></figcaption> +</figure></td></tr></table> + +<p id="exp-67"><span class="smcap">Experiment 67. What is the substance taken +in when oxygen is given off?</span>—Fill two glass +jars, or two tumblers, with water, to expel the +air, and invert in a shallow dish of water, having +first introduced a freshly cut sprig of some healthy +green plant into one of them. Then, by means +of a bent tube, blow into the mouth of each tumbler +till all the water is expelled by the impure air +from the lungs. Set the dish in the sunshine and +leave it, taking care that the end of the cutting is in +the water of the dish. After forty-eight hours remove +the tumblers by running under the mouth of +each, before lifting from the dish, a piece of glass well coated with vaseline +(lard will answer), and pressing it down tight so that no air can enter. +Place the tumblers in an upright position, +keeping them securely covered. Fasten a +lighted taper or match to the end of a wire, +plunge it quickly first into one tumbler, then +into the other, and note the result. What +was the gas blown from your lungs into the +jars? (Exps. 23, 24.) Why did the taper not +go out in the second jar? What had become +of the carbon dioxide?</p> + +<p id="exp-68"><span class="smcap">Experiment 68. To show that light +is necessary for a plant to absorb carbon dioxide and give off +oxygen.</span>—Repeat <a href="#exp-66">Exp. 66</a>, keeping the plant in a dark or shady place; +do you see any bubbles? Test with a glowing match; is any oxygen<span class="pagenum" id="Page_170">[Pg 170]</span> +formed in the tube of the funnel? Move back into the sunlight and +leave for a few hours; what happens when you thrust a glowing splinter +into the tube?</p> + +<p id="exp-69"><span class="smcap">Experiment 69. Is any food product found in leaves?</span>—Crush +a few leaves of bean, sunflower, or tropæolum, and soak in alcohol until all +the chlorophyll is dissolved out. Rinse them in water, and soak the +leaves thus treated in a weak solution of iodine for a few minutes, then +wash them and hold them up to the light. If +there are any blue spots on the leaves, what are +you to conclude? If a test for sugar is to be +made, use sap pressed from fresh leaves; for +oils and fats, leaves should be dried without +being placed in alcohol.</p> + +<figure class="figright illowp25" id="i_180" style="max-width: 23.625em;"> + <img class="w100" src="images/i_180.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 227.</span>—Leaf arranged +with a piece of tin foil to exclude +light from a portion of +the surface.</p></figcaption> +</figure> + +<p id="exp-70"><span class="smcap">Experiment 70. Has the presence or +absence of light anything to do with the +occurrence of starch in leaves?</span>—Exclude +the light from parts of healthy leaves on a growing +plant of tropæolum, bean, etc., by placing +patches of black cloth or paper over them. +Leave in a bright window, or preferably out of +doors, for several hours, and then test for starch +as in the last experiment; do you find any in +the shaded spots?</p> + +<p id="exp-71"><span class="smcap">Experiment 71. Is the presence of air necessary for the +production of starch?</span>—Cover the blades and the petioles of several +leaves with vaseline or other oily substance so as to exclude the air, and +after a day or two test as before.</p> +</div> + +<p id="p-185"><b>185. Influence of plants on the atmosphere.</b>—These +experiments show that leaves cannot do their work without +light and air. The particular element of the atmosphere +used by them in the process of food making is carbon dioxide. +Their action in absorbing this gas and giving off oxygen +tends to counterbalance the opposite action of respiration, +decomposition, and combustion of all kinds, by which the +proportion of it in the atmosphere tends to be constantly +increased. In this way they help to regulate the quantity +of it present and have a beneficial effect in ridding the air of +one source of impurity.</p> + +<p><span class="pagenum" id="Page_171">[Pg 171]</span></p> + +<p id="p-186"><b>186. Photosynthesis.</b>—In our examination of the internal +structure of the leaf, the chlorophyll bodies <a href="#p-184">(184)</a> were found +to contain small granules of starch which the chlorophyll, +under the stimulus of light, had elaborated as a nutriment for +the plant tissues. Hence, the leaf may be regarded as a +factory in which vegetable food, mainly starch, is manufactured +out of the water brought up from the soil, and the carbon +dioxide derived through the stomata from the atmosphere. +In this process carbon dioxide (CO<sub>2</sub>) is combined with water +(H<sub>2</sub>O) in such proportions that part of the oxygen is returned +to the surrounding air. This is a fundamental food-forming +process characteristic of green plants, and can take place +only in the light. For this reason it has been named <em>Photosynthesis</em>, +a word which means “building up by means of +light,” just as <em>photography</em> means “drawing or engraving +by means of light.”</p> + +<p>In carrying on the operation of photosynthesis, sunshine +is the power, the chlorophyll bodies the working machinery, +carbon dioxide and water the raw materials, and starch or oil +the finished product, while oxygen and the water of transpiration +represent the waste or by-products.</p> + +<p id="p-187"><b>187. How the new combination is effected.</b>—It may +seem strange that a gas and a liquid should combine to make +something so different from either as starch, but their chemical +constituents are the same in different proportions. Water +is made up of 2 parts hydrogen and 1 part oxygen; carbon +dioxide, of 1 part carbon and 2 parts oxygen, while starch +contains carbon, hydrogen, and oxygen, in the ratios of 6, +10, and 5, respectively. Hence, by taking sufficient quantities +of water and carbon dioxide and combining them in the +proper proportions, the leaf factory can turn them into +starch. If we use the letters C, H, and O, to represent Carbon, +Hydrogen, and Oxygen, respectively, the new combination +of materials can be expressed by an equation; thus:—</p> + + +<table class="autotable"> +<tr class="fs80"> +<td class="tdc"><i>water</i></td> +<td class="tdc"><i>carbon dioxide</i></td> +<td class="tdc"><i>starch</i></td> +<td class="tdc" colspan="2"><i>by-products</i></td> +</tr> +<tr> +<td class="tdc">5 (H<sub>2</sub>O)</td> +<td class="tdc">+ 6 (CO<sub>2</sub>) = </td> +<td class="tdc"> (C<sub>6</sub>H<sub>10</sub>O<sub>5</sub>) </td> +<td class="tdc">+ 6 (O<sub>2</sub>)</td> +<td class="tdc">= 12 (O).</td> +</tr> +</table> + +<p><span class="pagenum" id="Page_172">[Pg 172]</span></p> + +<p>The water not used up in the process is given off as a waste +product in transpiration, while the oxygen is returned to the +air, as shown by <a href="#exp-66">Exp. 66</a>. This equation is not to be understood +as representing the chemical changes that actually take +place in the leaf. These are too complicated, and at present +too imperfectly known, to be considered here. It will serve, +however, to give a fair idea of the final result from the process +of photosynthesis, however brought about.</p> + +<p>Simple as the operation appears, the chemist has not, as +yet, been able to imitate it. He can analyze starch into its +original constituents, but while he has the ingredients at +hand in abundance, and knows the exact proportions of their +combination, it is beyond his power, in the present state of +our knowledge, to put them together. Hence, both man +and the lower animals are dependent on plants for this most +important food element. The so-called factories that supply +the starch of commerce do not <em>make</em> starch any more than +the miller makes wheat, but merely separate and render +available for use that already elaborated by plants.</p> + +<p id="p-188"><b>188. Proteins.</b>—Foods of this class are mainly instrumental +in furnishing material for the growth and repair of +the tissues out of which the bodies of both plants and animals +are built up. They embrace a great variety of substances, +but their chemical nature is very complex and very imperfectly +understood. Nitrogen is an important element in +their composition, whence they are commonly distinguished +as “nitrogenous foods.” Besides nitrogen, there are present +carbon, hydrogen, oxygen, and sulphur, and traces of the +mineral salts absorbed from the soil are found in varying +quantities in the ash of different proteins. The percentages +in which these ingredients are combined and the processes +concerned in their formation are at present a matter of pure +hypothesis. Botanists are not agreed even as to whether +they are made in the leaf or in some other part or parts of +the plant, though the weight of opinion inclines to the view +that their construction takes place in the leaf.</p> + +<p><span class="pagenum" id="Page_173">[Pg 173]</span></p> + +<p id="p-189"><b>189. The activities of leaves.</b>—As there are only 4 parts +of CO<sub>2</sub> to every 10,000 parts of ordinary free air, it has been +estimated that in order to supply the leaf factory with the +raw material it needs, an active leaf surface of one square +meter—a little over one square yard—uses up, during +every hour of sunshine, the CO<sub>2</sub> contained in 1000 liters +(1000 quarts, approximately) of air. Suppose an oak tree +to bear 500,000 leaves, each having a surface of 16 sq. cm., or +4 sq. in., and working 12 hours a day for 6 months in the +year; you will then have some idea of the enormous quantity +of air that passes each season through its leaf system. Add +to this the almost incredible volume of water transpired in +the same time <a href="#p-180">(180)</a>, and we may well stand amazed at the +tremendous activities of these silent workers that we are in +the habit of regarding as mere passive elements in the +general landscape.</p> + +<p id="p-190"><b>190. The economic value of leaves.</b>—Besides their importance +as sanitary and food-making agencies, leaves have +a direct commercial value as food products in the hay and +fodder they supply for our domestic animals, the tea and +salads with which they provide our tables, the aromatic +flavors and seasonings contained in them, and the drugs, +medicines, and dyes of various kinds for which they furnish +the ingredients.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why do gardeners “bank” celery? (<a href="#exp-65">Exp. 65</a>.)</p> + +<p>2. Why are the buds that sprout on potatoes in the cellar, white? (<a href="#exp-65">Exp. +65</a>.)</p> + +<p>3. Why does young cotton look pale and sickly in long-continued wet +or cloudy weather? (<a href="#exp-65">Exp. 65</a>.)</p> + +<p>4. Why do parasitic plants generally have either no leaves or very +small, scalelike ones? (<a href="#p-85">85</a>, <a href="#p-186">186</a>, <a href="#p-187">187</a>.)</p> + +<p>5. The mistletoe is an exception to this; explain why, in the light of +your answer to question 4.</p> + +<p>6. Could an ordinary nonparasitic plant live without green leaves? +(<a href="#p-186">186</a>, <a href="#p-187">187</a>.)</p> + +<p>7. Are abundance and color of foliage any indication of the health of +a plant? (<a href="#p-186">186</a>, <a href="#p-187">187</a>; <a href="#exp-65">Exp. 65</a>.)</p> + +<p><span class="pagenum" id="Page_174">[Pg 174]</span></p> + +<p>8. Is the practice of lopping and pruning very closely, as in the process +called “pollarding,” beneficial to a tree under ordinary conditions? (<a href="#p-186">186</a>, +<a href="#p-189">189</a>; <a href="#exp-63">Exp. 63</a>.)</p> + +<p>9. Name some plants of your neighborhood that grow well in the shade.</p> + +<p>10. Compare in this respect Bermuda grass and Kentucky blue grass; +cotton and maize; horse nettle (<i>Solanun Carolinense</i>) and dandelion; +beech, oak, red maple, dogwood, pine, cedar, holly, magnolia, etc.</p> + +<p>11. Name all the aromatic leaves you can think of; all that are used as +food, beverages, drugs, and dyes.</p> + +<p>12. What is the use of aromatic and medicinal leaves to the plant itself? +(Suggestion: Why does the housewife put lavender or tobacco leaves in +her woolen chest?)</p> + +<p>13. Which would be richer in nourishment, hay cut in the evening or +in the morning, and why? (<a href="#p-54">54</a>, <a href="#p-186">186</a>; <a href="#exp-70">Exp. 70</a>.)</p> + +<p>14. Mention three important sanitary services that are rendered by a +tree like that shown in <a href="#i_127">plate 6</a> or <a href="#i_140">8</a>. (<a href="#p-180">180</a>, <a href="#p-185">185</a>, <a href="#p-189">189</a>.)</p> + +<p>15. Name some of the plants employed in the manufacture of starch.</p> +</div> + + +<h3 id="CH_VI_VI">VI. THE LEAF AN ORGAN OF RESPIRATION</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A number of vigorous, freshly cut green leaves; a liter +or two (one or two quarts) of expanding flower or leaf buds.</p> + +<p><span class="smcap">Appliances.</span>—Some wide-mouthed jars of one or two liters’ capacity; +two small open vials of limewater.</p> + +<p id="exp-72"><span class="smcap">Experiment 72. Do leaves give off carbon dioxide?</span>—Cover +the bottoms of two wide-mouthed jars with water about two centimeters +(1 inch) deep. Place in one a number of healthy green leaves with +their stalks in the water, and insert among them a small open vial containing +limewater. In the other jar place only a vial of limewater in the +clear water at the bottom, this last being merely to make the conditions +in both vessels the same. Seal both tight and keep together in the dark +for about 48 hours, and then examine. In which jar does the limewater +indicate the greater accumulation of CO<sub>2</sub>? (It may show a slight +milkiness in the other vessel due to gas derived from the inclosed air and +water.) From this experiment, what process would you conclude has +been going on among the leaves in jar No. 1? (<a href="#exp-25">Exp. 25</a>.)</p> + +<figure class="figright illowp25" id="i_185" style="max-width: 17.25em;"> + <img class="w100" src="images/i_185.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 228.</span>—Arrangement +of apparatus to +show that heat and carbon +dioxide are given off +by leaf buds.</p></figcaption> +</figure> + +<p id="exp-73"><span class="smcap">Experiment 73. Is the exhalation of carbon dioxide accompanied +by any other concomitant of respiration?</span>—In <a href="#exp-24">Exps. 24</a>, +<a href="#exp-25">25</a>, it was shown that respiration is accompanied by heat; hence, if the +production of carbon dioxide by the leaf is due to this cause, it should be +attended by the evolution of heat. To find out whether this is the case, +partly fill a glass jar of two liters’ capacity with unfolding leaf buds arranged<span class="pagenum" id="Page_175">[Pg 175]</span> +in layers alternating with damp cotton batting +or blotting paper (<a href="#i_185">Fig. 228</a>); close the jar +tightly and leave from 12 to 24 hours in the dark +to prevent the action of photosynthesis. Then +insert a thermometer and note the rise in temperature. +If a lighted taper is plunged in, it will +quickly be extinguished, showing that respiration +has been going on.</p> +</div> + +<p id="p-191"><b>191. Respiration in leaves.</b>—We see +from experiments like the foregoing that +the leaf, besides carrying on the functions +of digestion, photosynthesis, and transpiration, +is also an active agent in the +work of respiration. In this function +oxygen is used up and carbon dioxide +given off, just as in the respiration of animals; but the +process is so slow in plants that it is much more difficult +to detect than the contrary action in photosynthesis, and is, +in fact, not perceptible at all while the latter is going on, +though it does not cease even then.</p> + +<p>But while the leaf is the principal organ of respiration, the +process is carried on in other parts of the plant as well, +else it could not survive during the leafless months of +winter. It <em>appears</em> to be most active at night, but this is +only because it is not obscured then, as during the day, by +the more active function of photosynthesis. Indeed, it was +for a long time supposed that plants “breathed” only at +night, and it was thought to be unwholesome to keep them +in a bedroom. It is now known, however, that respiration +goes on at all times and in all living parts of the plant, but +the quantity of oxygen taken in is so small from a hygienic +point of view that it may be disregarded.</p> + +<p id="p-192"><b>192. Distinctions between respiration and photosynthesis.</b>—While +these two functions are contrasting and antipodal, +so to speak, in their action, they are mutually complementary +and interdependent, the one manufacturing food and the +other using it up, or rather marking the activity of those<span class="pagenum" id="Page_176">[Pg 176]</span> +life processes by which it is used up. The difference between +them will be made clear by a comparison of the two processes +as summarized in the following statement:</p> + + +<table class="autotable fs80 wd80 statement"> +<tr> +<th class="tdc smcap wd50">Photosynthesis</th> +<th class="tdc smcap wd50 pl1">Respiration</th> +</tr> +<tr> +<td class="tdl vat pr1"><p>Goes on only in sunlight and in the green parts of plants.</p></td> +<td class="tdl vat pl1"><p>Goes on at all times and in all parts of the plant.</p></td> +</tr> +<tr> +<td class="tdl vat pr1"><p>Produces starch and sugar.</p></td> +<td class="tdl vat pl1"><p>Releases energy (heat and working power).</p></td> +</tr> +<tr> +<td class="tdl vat pr1"><p>Gives off, as by-product, oxygen.</p></td> +<td class="tdl vat pl1"><p>Gives off, as by-products, CO<sub>2</sub> and water.</p></td> +</tr> +<tr> +<td class="tdl vat pr1"><p>A constructive process, in which energy is used up to make food.</p></td> +<td class="tdl vat pl1"><p>A destructive, or consumptive process, in which food is used up in expending energy.</p></td> +</tr> +</table> + + +<p id="p-193"><b>193. Metabolism.</b>—The total of all the life processes of +plants, including growth, waste, repair, etc., is summed up +under the general term <em>metabolism</em>. It is a <em>constructive</em> or +building-up process when it results in the making of new +tissues out of food material absorbed from the earth and air, +and the consequent increase of the plant in size or numbers. +But, as in the case of animals, so with plants, not all the +food provided is converted into new tissue, part being used +as a source of energy, and part decomposed and excreted +as waste. In this sense, metabolism is said to be <em>destructive</em>. +The waste in healthy growing plants is always, of course, less +than the gain, and a portion of the food material is laid by +as a reserve store. For this reason, photosynthesis, being a +constructive process, is usually more energetic than respiration, +which is the measure of the destructive change of +materials that attends all life processes.</p> + +<p>It is evident also, from what has been said, that growth and +repair of tissues can take place only so long as the plant has +sufficient oxygen for respiration, since the energy liberated +by it is necessary for the assimilation of nourishment by +the tissues.</p> + +<p>Thus we see that plants are dependent on air not only for +respiration, but for nutrition, and none of their life processes +can be carried on without it.</p> + +<p><span class="pagenum" id="Page_177">[Pg 177]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Can a plant be suffocated, and if so, in what ways? (<a href="#p-87">87</a>, <a href="#p-193">193</a>; +Exps. 26, 27.)</p> + +<p>2. The roots on the palm shown in <a href="#i_083">plate 3</a> are not drawing any sap +from it as parasites; why does their continued growth bring about the +death of the tree? (<a href="#p-87">87</a>, <a href="#p-193">193</a>.)</p> + +<p>3. Is it unwholesome to keep flowering plants in a bedroom? Leafy +ones? Why, in each case? (<a href="#p-191">191</a>.)</p> + +<p>4. Would there be any more reason for objecting to the presence of +flowers by night than by day? Explain. (<a href="#p-191">191</a>.)</p> + +<p>5. Why is respiration much less marked in plants than in animals? +(<a href="#p-30">30</a>, <a href="#p-31">31</a>.)</p> +</div> + + +<h3 id="CH_VI_VII">VII. THE ADJUSTMENT OF LEAVES TO EXTERNAL +RELATIONS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A potted plant of oxalis, spotted medick, white clover, +or other sensitive species. The subject is better suited for outdoor observation +than for laboratory work.</p> + +<p id="exp-74"><span class="smcap">Experiment 74. To show that leaves adjust themselves to +changes in intensity of light.</span>—Keep a healthy potted plant of oxalis, +white clover, or spotted medick in +your room for observation. Note +the daily changes of position the +leaves undergo. Sketch one as it +appears at night and in the morning.</p> + +<figure class="figright illowp40" id="i_187" style="max-width: 30em;"> + <img class="w100" src="images/i_187.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 229, 230.</span>—Leaves of a peanut +plant: 229, in day position; 230, in +night position.</p></figcaption> +</figure> + +<p>In order to determine whether +these changes are due to want of light +or of warmth, put your plant in a dark +closet in the middle of the day, without +change of temperature. After +several hours note results. Transfer +to a refrigerator, or in winter place +outside a window where it will be exposed +to a temperature of about 5° C. (40° F.) for several hours, and see if +any change takes place. Next put it at night in a well-lighted room and +note the effect. If practicable, keep a specimen for several weeks in some +place where electric lights are burning continuously all night, and watch +the results.</p> + +<p id="exp-75"><span class="smcap">Experiment 75. To show that the fall of the leaf may result +from other causes than cold or frost.</span>—Wrap some leaves of ailanthus, +Kentucky coffee tree, ash, walnut, or hickory in a damp towel and<span class="pagenum" id="Page_178">[Pg 178]</span> +keep them in the dark for several days; the leaflets will fall away, leaving +a clear scar like those on winter twigs.</p> + +<p id="exp-76"><span class="smcap">Experiment 76. To show that adjustments to temperature may +be made by chemical means.</span>—Place a small twig of oleander, laurestinus, +or other broad-leaved evergreen in a 5 to 10 per cent solution +of sugar, and transfer it at the end of a few days to a temperature of +6° to 8° below freezing. On comparison with a similar twig that has +stood for the same length of time in pure water, it will be found to possess +a greater power of resistance to cold.</p> +</div> + +<figure class="figright illowp30" id="i_188" style="max-width: 20em;"> + <img class="w100" src="images/i_188.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 231.</span>—A +plant that has been +growing near an open +window, showing the +leaves all turned +toward the light.</p></figcaption> +</figure> + +<p id="p-194"><b>194. The light relation.</b>—The principal external conditions +to which leaves have to adjust themselves are light, +air, moisture, gravity, temperature, and the attacks of animals. +From the knowledge of their work and function +gained in the preceding sections, it will be clear that the primary +relation of the leaf is a light relation, and to this, first of +all, it must adjust itself.</p> + +<p>It was shown in Exps. 56 and 57 how promptly leaves respond +to changes in the direction of light, +and a little observation (<a href="#exp-74">Exp. 74</a>) will convince +us that they are equally sensitive to +changes in intensity and periodicity of illumination.</p> + +<p id="p-195"><b>195. Phototropism.</b>—The movement of +plants in response to light is called <em>phototropism</em>—a +word that means “turning +toward or away from light.” It includes +all kinds of light adjustments, and examples +of it are to be met with everywhere in the +disposition of leaves with reference to their +light exposure.</p> + +<p id="p-196"><b>196. Horizontal and vertical adjustment.</b>—Take two +sprigs, one upright, the other horizontal, from any convenient +shrub or tree—and notice the difference in the position of +the leaves. Examine their points of attachment and see how +this is brought about, whether by a twist of the petiole or of +the base of the leaf blades, or by a half twist of the stem +between two consecutive leaves, or by some other means.</p> + +<p><span class="pagenum" id="Page_179">[Pg 179]</span></p> + +<figure class="figcenter illowp52" id="i_189" style="max-width: 75em;"> + <img class="w100" src="images/i_189.jpg" alt=""> + <figcaption><p class='pm0'><span class="smcap">Plate 10.</span>—A mosaic of moonseed leaves, showing adjustment for light exposure.</p> + <p class='center pm0'>(<i>From</i> Mo. Botanical Garden Rep’t.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_180">[Pg 180]</span></p> + +<p>Observe both branches in their natural position; what part +of the leaf is turned upward, the edge or the surface of the +blade? Change the position of the two sprigs, placing the +vertically growing one horizontal, and the horizontal one +vertical. What part of the leaves is turned upward in each?</p> + +<figure class="figcenter illowp75" id="i_190" style="max-width: 52.6875em;"> + <img class="w100" src="images/i_190.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 232, 233.</span>—Adjustment of leaves to different positions: +232, upright; 233, procumbent.</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_190a" style="max-width: 21.875em;"> + <img class="w100" src="images/i_190a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 234.</span>—Leaf mosaic +of elm.</p></figcaption> +</figure> + +<p id="p-197"><b>197. Leaf mosaics.</b>—Trees with horizontal or drooping +branches, like the elm and beech, and vines growing along +walls or trailing on the ground, generally display their foliage +in flat, spreading layers, each leaf fitting +in between the interstices of the +others like the stones in a mosaic, +whence this has been called the <em>mosaic</em> +arrangement. (<a href="#i_189">Plate 10</a>.) In plants of +more upright or bunchy habit, the +leaves are placed at all angles, giving +the appearance of a rosette when viewed +from above, whence this is called the +<em>rosette</em> arrangement.</p> + +<p>A variety of the same disposition is +seen in the pyramidal shape assumed +by plants with large, undivided leaves +like the mullein and burdock (<a href="#i_191a">Fig. 237</a>), in which access of +light is secured by a mutual adjustment between the size +and position of leaves, the upper ones becoming successively +smaller.</p> + +<p><span class="pagenum" id="Page_181">[Pg 181]</span></p> + +<p id="p-198"><b>198. Heliotropism</b>—“turning +with the sun”—is +the name given to the daily +movement of plants like the +cotton and sunflower in +turning their leaves or their +blossoms to face the sun. If you live where cotton is grown, +notice the leaves in a field about ten o’clock on a bright +sunny morning, and again from the same +point of view at about four or five in the +afternoon. Do you perceive any difference +in their general disposition? +Watch on a +cloudy day and see if +any change takes place. +Find out by observation +whether the “heliotrope” +of the hothouses is really +heliotropic.</p> + +<figure class="figcenter illowp90" id="i_191" style="max-width: 99em;"> + <img class="w100" src="images/i_191.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 235, 236.</span>—Horse-chestnut leaves: 235, leaf rosette seen from above; +236, the same seen sidewise, showing the formation of rosettes by the lengthening +of the lower petioles.</p></figcaption> +</figure> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp70" id="i_191a" style="max-width: 25em;"> + <img class="w100" src="images/i_191a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 237.</span>—Leaf +pyramid of mullein.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp70" id="i_191b" style="max-width: 28em;"> + <img class="w100" src="images/i_191b.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 238, 239.</span>—A +compass plant, rosinweed +(<i>Silphium laciniatum</i>): +238, seen from +the east; 239, seen +from the south.</p></figcaption> +</figure></td></tr></table> + +<p id="p-199"><b>199. Adjustment +against too great intensity +of light.</b>—Plants frequently +have to protect +themselves against excess +of light and heat. An<span class="pagenum" id="Page_182">[Pg 182]</span> +interesting example of this kind of adjustment is furnished +by the rosinweed, or compass plant (<i>Silphium laciniatum</i>, +<a href="#i_191b">Figs. 238, 239</a>), which grows in the prairies of Alabama and +westward, where it is exposed to intense sunlight. The +leaves not only stand vertical, but have a tendency to turn +their edges north and south so that the blades are exposed +only to the gentler morning and evening rays. The prickly +lettuce manifests the same habit in a less marked degree.</p> + +<figure class="figright illowp50" id="i_192" style="max-width: 38em;"> + <img class="w100" src="images/i_192.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 240, 241.</span>—A plant of the guayule +(<i>Parthenium argentatum</i>), to the leaves of which +indexes have been affixed to show their day and +night position: 240, day position; 241, night +position. (<i>From</i> photographs by Prof. F. E. +Lloyd.)</p></figcaption> +</figure> + +<p id="p-200"><b>200. Night and day adjustments.</b>—These are movements +in response to changes in the degree of illumination +and temperature, as evidenced by the fact that they become +feeble and soon cease altogether if the plant is kept a sufficient +time under uniform conditions as to these two factors. +(<a href="#exp-74">Exp. 74</a>.) They are called “nyctitropic” or sleep movements, +because they are most obvious in certain plants that +undergo periodic adjustments to the alternations of day and +night suggestive of an imaginary likeness to the sleep of animals. +Examples are +most frequently met +with among members of +the pea family (<i>Leguminosæ</i>), +the spurges +(<i>Euphorbiaceæ</i>), and the +sorrel (<i>Oxalis</i>) family. +They are found among +other species also, and +indeed are much more +general than is usually +supposed, most plants +showing signs of them +if carefully tested. A +simple way of doing this +is by attaching bristles about two inches long to the tips of +two leaves on opposite sides of the stem, as in <a href="#i_192">Figs. 240, 241</a>, +and comparing the divergence of the bristles during the day +and at nightfall. In this way a change of position in the<span class="pagenum" id="Page_183">[Pg 183]</span> +leaves, too slight to attract attention otherwise, will be made +apparent. The positions assumed vary in different plants, +and even in the parts of the same compound leaf; in the +kidney bean, for instance, the common petiole turns up at +night, while the individual leaflets turn down. One of the +common pigweeds (<i>Amaranthus Palmeri</i>, <a href="#i_193">Figs. 242-244</a>) is +heliotropic in the day time and nyctitropic at night.</p> + +<figure class="figcenter illowp90" id="i_193" style="max-width: 50em;"> + <img class="w100" src="images/i_193.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 242-244.</span>—Showing the movements of <i>Amaranthus Palmeri</i>: 242, 243, +position at sunrise and sunset (heliotropic); 244, night position (nyctitropic) half an +hour after sunset. (<i>From</i> photographs by Prof. F. E. Lloyd.)</p></figcaption> +</figure> + +<p>The very striking nyctitropic adjustments of the wild +senna (<i>Cassia tora</i>) photographed by Professor Francis<span class="pagenum" id="Page_184">[Pg 184]</span> +E. Lloyd of the Alabama Polytechnic Institute (<a href="#i_193a">Figs. 245-250</a>), +though obviously influenced by the sun, are not +directed toward it as in those of truly heliotropic plants.</p> + +<figure class="figcenter illowp90" id="i_193a" style="max-width: 53.25em;"> + <img class="w100" src="images/i_193a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 245-250.</span>—Wild senna (<i>Cassia tora</i>), showing the nyctitropic adjustments +of its leaves. The upper figures show their horizontal arrangement; those below, +the vertical: 245, 248, position of the leaves at 9 <span class="allsmcap">A.M.</span>; 246, 249, at 3 <span class="allsmcap">P.M.</span>; 247, +250, at 6.30 <span class="allsmcap">P.M.</span> (<i>From</i> photographs by Prof. F. E. Lloyd.)</p></figcaption> +</figure> + +<p>These movements are common also among flowers, many +of them having regular hours for opening and closing, as indicated +by such names as “morning-glory” and “four-o’clock.” +In these cases, however, other causes (<a href="#p-277">277</a>, <a href="#p-280">280</a>) +than the light relation must be taken into account.</p> + +<p id="p-201"><b>201. Irritability</b> is a general term applied to the power in +plants of receiving and responding by spontaneous movements +to impressions from without. In its widest acceptation, +irritability includes, besides the various forms of +adjustment described in this section and the next, all movements +due to geotropism, those of roots seeking air and moisture, +the revolution of twining stems and tendrils, the circulation +of protoplasm in the cell—any movement, in short, +that is made in response to an impression from the environment +is a manifestation of irritability. It may be of various +degrees, but is possessed to some extent by every living vegetable +organism.</p> + +<p>The term is usually applied, however, more especially to +those obvious and pronounced responses made by plants to +their surroundings, as exemplified in the cases just given. +Still more marked instances are to be found in the movements +of the tentacles of insectivorous plants, and the sensitive +leaflets of the mimosa that close at the slightest touch. The +tendrils of the passion flower are said to appreciate and +respond to a pressure that cannot be distinguished even by +the human tongue, and many plants will detect and respond +to the ultra-violet rays of light, which are entirely invisible +to man.</p> + +<p>This faculty of irritability among plants corresponds, in an +imperfect, rudimentary way, to what we recognize in animals +as nervous excitability. By this it is not meant to imply +that the two things are identical in their ultimate manifestations, +though we may regard them as fundamentally the<span class="pagenum" id="Page_185">[Pg 185]</span> +same in that they are both to be referred to the property +inherent in protoplasm of responding to stimuli. There is +no indication, however, that irritability in the vegetable +kingdom is accompanied by anything like consciousness or +volition, or that plants possess any power of initiative. +While the movements in response to stimuli are in many +cases eminently adapted to a purpose, we have no evidence +of a controlling power behind them. The movement comes +automatically in response to the stimulus, whether the effect +at the moment be advantageous or the +reverse.</p> + +<p id="p-202"><b>202. Adjustments in relation to +moisture.</b>—These adjustments may +be—(1) To guard against excess of +moisture; <i>e.g.</i> glands for excreting water +and salts; scales, wax, down, etc., on +the surface of leaves. These may serve +also for protection against cold, insects, +excess of light and heat. (2) For the +conservation of moisture; <i>e.g.</i> the revolute +leaf margins of grasses and sand plants growing along +the seashore; the fleshy leaves of stonecrops and purselanes; +the hard epidermis of yuccas and aloes; the scales, scurf, and +down, by which the moisture absorbed from the soil by plants +growing in dry and barren +places is prevented +from escaping too +rapidly through the +stomata; the leaf cups +and holders sometimes +formed by winged +petioles and clasping +leaf bases for retaining +dew or rain water. +(3) For leaf drainage, +or the conduction of<span class="pagenum" id="Page_186">[Pg 186]</span> +moisture, by means of grooves, channels, and taper-pointed +leaves, which act as natural gutters and drain pipes.</p> + +<table> +<tr><td> +<figure class="figcenter illowp90" id="i_195" style="max-width: 21.25em;"> + <img class="w100" src="images/i_195.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 251.</span>—Cross sections +of the leaf of sand +grass: <i>a</i>, unrolled in its ordinary +position; <i>b</i> and <i>c</i>, +rolled up to prevent too +rapid transpiration.</p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp90" id="i_195_252" style="max-width: 24.375em;"> + <img class="w100" src="images/i_195_252.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 252.</span>—Winged petiole of <i>Polymnia</i>.</p> + </figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp90" id="i_195_253" style="max-width: 24.375em;"> + <img class="w100" src="images/i_195_253.jpg" alt=""> + <figcaption> + <p><span class="smcap">Fig. 253.</span>—Water cups of <i>Silphium perfoliatum</i>.</p> + </figcaption> +</figure></td></tr></table> + +<figure class="figright illowp50" id="i_196" style="max-width: 50.75em;"> + <img class="w100" src="images/i_196.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 254.</span>—Fallen leaves. Notice how they cover +the ground with a warm mulch, protecting the soil +from denudation, and the roots and seeds from frost.</p></figcaption> +</figure> + +<p id="p-203"><b>203. The fall of the leaf.</b>—This is, in effect, an adjustment +to change of temperature, but that it is not directly due +to cold is shown by <a href="#exp-75">Exp. 75</a>, and also by the fact that leaves +in the tropics and those of evergreens, while they do not fall +at stated periods like the bulk of the foliage in the temperate +zones, are cut off just the same and replaced by new ones, +whenever, for any +reason, they are unable +to perform their +function. In cold +climates they fall at +the approach of +winter, not because +the frost loosens +them, but because +the roots are not able +to absorb enough +moisture to supply +them with material +for making food. +The needles and the +scale-leaves characteristic +of evergreens +in cold regions are +enabled to persist indefinitely by reason of their contracted +surface. This prevents the dissipation of moisture and affords +no lodging for the accumulations of sleet and snow that +would otherwise cumber and perhaps break the boughs with +their weight. Trees and shrubs that shed their leaves in winter +are said to be <em>deciduous</em>, from a Latin word meaning “to +fall.” Can you mention some advantages of the deciduous +habit to a plant with broad, expanded leaves, growing in +a cold climate?</p> + +<p>The mechanical means by which the leaf fall is accomplished<span class="pagenum" id="Page_187">[Pg 187]</span> +is through the growth of a corky layer of loose +cells that forms at the base of the petiole and cuts it away +from the stem, leaving a smooth, clean scar. Tear some +fresh young leaves from a growing twig and compare the +scars with those on a winter bough. Do you see any +difference? This corky layer can be made to form in +some plants artificially, by depriving them of working material. +(<a href="#exp-75">Exp. 75</a>.)</p> + +<p id="p-204"><b>204. The protection of wintergreen leaves.</b>—A great +many, perhaps the majority of broad-leaved evergreens, +bear no obvious protection against cold, while a large proportion, +such as chickweed, violet, fumitory, groundsel +(<i>Senecio</i>), and dead nettle (<i>Lamium</i>), would seem peculiarly +unfitted, by their delicate structure, to withstand it. But +recent investigations by the Swedish botanist, Lidforss, +have shown that all wintergreen leaves, with the exception +of those on submerged water plants, which are sufficiently +protected by the medium in which they live, lose their +starch in winter and contain instead an increased percentage +of sugar. The same is true of other vegetable structures +also, where starch is present, such as roots, stems, tubers, +and winter fruits—nuts, haws, persimmons, and the like, +which, as every schoolboy knows, become perceptibly sweeter +after frost.</p> + +<p>The presence of certain substances, of which sugar is the +most frequent, enables plants to withstand a greater degree +of cold than they could otherwise endure (<a href="#exp-76">Exp. 76</a>). This +effect, as shown by Lidforss’s experiments, is due to the +action of sugar in counteracting, or retarding, the “salting +out” of proteins by cold, as explained in 33.</p> + +<p>As sugar is readily reconverted into starch by exposure to +a moderately high temperature for even a few days, we may +find here an explanation of the fact that plants which have +survived the prolonged cold of winter are often killed by a +single sharp night frost following a few warm days in early +spring, before the tender new growth has appeared. The<span class="pagenum" id="Page_188">[Pg 188]</span> +plant suffers, not from the direct effects of cold, but from +the warmth preceding it, which stimulated the transformation +into starch of the sugar that would have prevented the +loss of proteins. On the same principle we may account for +the puzzling fact that the sunny southern side of trees and +shrubs usually suffers more from the effects of sudden frost +than the shaded and colder northern face.</p> + +<p>In apparent conflict with this reasoning is the fact that +sugar cane and the sugar beet are peculiarly susceptible to +cold. This, however, does not invalidate the premises established +by Lidforss’s researches, but merely emphasizes +the need of further investigation, which may either reconcile +all the facts, or modify their interpretation.</p> + +<p id="p-205"><b>205. The colors of autumn leaves.</b>—These are due to +the breaking up and disappearance of the chlorophyll when +the leaf factory has to “shut down” for want of raw material +to work with <a href="#p-203">(203)</a>. It is closely connected with the +appearance of frost, since the same changes of temperature +which produce frost cause the cessation of sap flow that +brings about the disorganization of the chlorophyll and the +formation of various pigments derived from it. Besides +these, leaves may contain other coloring matters that are +perceptible only when the chlorophyll disappears; and in +the sap there is a reddish pigment which becomes either a +very bright red, or a dark purplish maroon, from the effect +of chemicals that combine with it in the leaves. With these +coloring materials at command it is easy to see how the +autumn woods can assume such splendid hues.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. How would you explain the fact that the outer twigs of trees generally +are the most leafy? (<a href="#p-99">99</a>, <a href="#p-194">194</a>; <a href="#exp-57">Exps. 57</a>, <a href="#exp-74">74</a>.)</p> + +<p>2. Is the common sunflower a compass plant? Is cotton?</p> + +<p>3. Are there any such plants in your neighborhood?</p> + +<p>4. Compare the leaves of half a dozen shade-loving plants of your neighborhood +with those of as many sun-loving ones; which, as a general thing, +are the larger and less incised?</p> + +<p><span class="pagenum" id="Page_189">[Pg 189]</span></p> + +<p>5. Give a reason for the difference. (<a href="#p-169">169</a>.)</p> + +<p>6. Why do most leaves—notably grasses—curl their edges backward +in withering? (<a href="#p-182">182</a>.)</p> + +<p>7. What advantage is gained by doing this? (<a href="#p-202">202</a>.)</p> + +<p>8. Observe such of the following plants as are found in your neighborhood, +and report any changes of position that may take place in their +leaves and the causes to which such changes should be ascribed: wood +sorrel, mimosa, honey locust, wild senna, partridge pea, wild sensitive plant, +redbud, bush clover, Japan clover, Kentucky coffee tree, sensitive brier +(<i>Schrankia</i>), peanut, kidney bean.</p> + +<p>9. Which of the trees named below shed their leaves from base to tip +of the bough (centripetally), and which in the reverse order: ash, beech, +hazel, hornbeam, lime, willow, poplar, pear, peach, sweet gum, elm, sycamore, +mulberry, China tree, sumac, chinquapin?</p> + +<p>10. Account for the fact that evergreen trees and shrubs have generally +thick, hard, and shiny leaves, like those of the holly and magnolia, or scales +and needles, as the cedar and pine. (<a href="#p-203">203</a>.)</p> + +<p>11. Why do many plants which are deciduous at the North tend to become +evergreen at the South? (<a href="#p-203">203</a>.)</p> + +<p>12. Why are evergreens more abundant in cold than in warm climates? +(<a href="#p-203">203</a>.)</p> + +<p>13. There is an apparent inconsistency between questions 11 and 12; +can you reconcile it? (<a href="#p-203">203</a>.)</p> + +<p>14. Why is it more important to protect the south side of trees against +exposure to frost than the northern side? (<a href="#p-33">33</a>, <a href="#p-204">204</a>.)</p> + +<p>15. Explain why peach orchards on the tops and northern slopes of elevated +areas are less liable to have their fruit destroyed by late frost than +those in the valleys and on the southern slopes. (<a href="#p-33">33</a>, <a href="#p-204">204</a>.)</p> +</div> + + +<h3 id="CH_VI_VIII">VIII. MODIFIED LEAVES</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Get from a florist a potted plant of sundew, Venus’s-flytrap, +sarracenia, or, if possible, one of all three, and keep in the schoolroom +for observation. The subject can be studied best in a well-stocked +greenhouse, if one is accessible.</p> +</div> + +<figure class="figright illowp40" id="i_200" style="max-width: 37.375em;"> + <img class="w100" src="images/i_200.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 255.</span>—Spearlike leaves of Spanish +bayonet.</p></figcaption> +</figure> + +<p id="p-206"><b>206. Modification and adaptation.</b>—Modification is +structural adjustment, or adaptation, carried so far as to +obscure the original form of an organ. Its true nature, +however, can generally be determined by some of the tests +mentioned in <a href="#p-100">100</a>.</p> + +<p>Examples of the modification of leaves to do the work of<span class="pagenum" id="Page_190">[Pg 190]</span> +other organs have already been noticed, as also their entire +disappearance in certain cases (<a href="#p-97">97</a>, <a href="#p-101">101</a>, <a href="#p-149">149</a>) and replacement +by other parts; it is +unnecessary, therefore, to +revert to this branch of the +subject here.</p> + +<p id="p-207"><b>207. Protective modifications.</b>—The +most general +protective modifications +that leaves undergo are +(1) for the conservation of +moisture, as explained in +<a href="#p-202">202</a>, and (2) for protection +against animals. Many of +the adaptations for the +former purpose serve incidentally +for defense against +animals also. Spines, hairs, +scales, sticky exudations, +water holders, clasping and +perfoliate leaves bar the way to crawling insects; horny +cuticles, as well as offensive odors, bitter secretions, and +poisonous juices warn leaf-eating cattle and bugs away. +These devices are merely protective, however, and adapted +to a passive attitude of self-defense.</p> + +<figure class="figcenter illowp90" id="i_200a" style="max-width: 50em;"> + <img class="w100" src="images/i_200a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 256-258.</span>—Protective hairs magnified: 256, mullein; 257, cinque-foil +258, Shepherdia.</p></figcaption> +</figure> + +<p id="p-208"><b>208. Insectivorous leaves.</b>—But sometimes a plant<span class="pagenum" id="Page_191">[Pg 191]</span> +becomes the aggressor, and instead of standing on the defensive +or suffering itself to be quietly devoured, proceeds to +capture and devour small game on its own account, and in +this case, the leaf sometimes becomes a deadly weapon of +destruction.</p> + +<p id="p-209"><b>209. Pitcher plants.</b>—The sarracenia, or trumpet leaf, +is a familiar example of this class. The lower part of the +leaf blade is transformed +into a hollow vessel for +holding water, and the +top is rounded into a +broad flap called the +<em>lamina</em>. Sometimes the +lamina stands erect, as +in the common yellow +trumpets of our coast +regions, and when this is +the case, it is brilliantly +colored and attracts insects +(<a href="#i_201">Fig. 259</a>). Sometimes, +as in the parrot-beaked +and the spotted +trumpet leaf, it is bent +over the top of the water +vessel like a lid, and the +back of the leaf, near the foot of the lamina, is dotted with +transparent specks that serve to decoy foolish flies away +from the true opening and tempt them to wear themselves +out in futile efforts to escape, as we often see them do against +a window pane.</p> + +<table> +<tr><td> +<figure class="figcenter illowp80" id="i_201" style="max-width: 43.75em;"> + <img class="w100" src="images/i_201.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 259.</span>—Yellow trumpets (<i>Sarracenia flava</i>). +(<i>From</i> the Mo. Botanical Garden Rep’t.)</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_202" style="max-width: 28.75em;"> + <img class="w100" src="images/i_202.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 260.</span>—Plant of sundew.</p></figcaption> +</figure></td></tr></table> + +<p>If the contents of one of these leaves are examined with a +lens, there will generally be found mixed with the water at the +bottom the remains of the bodies of a large number of insects. +The hairs on the outside all point up, toward the +rim of the pitcher, while those on the inside turn down, +thus smoothing the way to destruction, but making return<span class="pagenum" id="Page_192">[Pg 192]</span> +impossible to a small insect when once it is ensnared. +When we remember that these plants are generally found +in poor, barren soil, we can appreciate +the value to them of the animal +diet thus obtained.</p> + +<figure class="figcenter illowp90" id="i_202a" style="max-width: 50em;"> + <img class="w100" src="images/i_202a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 261-263.</span>—Leaves of sundew magnified: 261, leaf expanded; 262, leaf +closing over captured insect; 263, leaf digesting a meal.</p></figcaption> +</figure> + +<p id="p-210"><b>210. Flytraps.</b>—The most remarkable +examples of insect-catching +leaves are the Venus’s-flytrap, +found in the seacoast region of +North Carolina, and the sundew +(<i>Drosera rotundifolia</i>), common on +the margins of sandy bogs and +ponds. The latter is a delicate, +innocent-looking little plant, and +owes its poetic name to the dewlike +appearance of a shining, sticky +fluid exuded from glands on its +leaves, which glitter in the sun like dewdrops. It is, however, +a most voracious carnivorous plant, the sticky leaves acting +as so many bits of fly paper by means of which it catches its +prey. When a fly has been trapped, the tentacles close +upon it, the edges of the leaf curve inward, making a sort of +stomach, from the glands of which an acid juice exudes and<span class="pagenum" id="Page_193">[Pg 193]</span> +digests the meal. After a number of days, varying according +to the digestibility of the diet, the blades slowly unfold again +and are ready for another capture.</p> + +<figure class="figcenter illowp90" id="i_203" style="max-width: 50em;"> + <img class="w100" src="images/i_203.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 264.</span>—Bladderwort, showing finely dissected submerged leaves +bearing bladders for capturing animalculæ.</p></figcaption> +</figure> + +<p>The bladderwort, common in pools and still waters nearly +everywhere, has its petioles transformed into floats, while +the finely dissected, rootlike blades bear little bladders which, +when examined under the microscope, are found to contain +the decomposed remains of captured animalculæ.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Can you find any kind of leaf that is not preyed upon by something? +If so, how do you account for its immunity?</p> + +<p>2. Make a list of some of the most striking of the protected leaves of +your neighborhood.</p> + +<p>3. What is the nature of the protective organ in each case?</p> + +<p>4. For protection against what does it seem to be specially adapted?</p> + +<p>5. Are the plants in your list for the most part useful ones, or troublesome +weeds?</p> + +<p><span class="pagenum" id="Page_194">[Pg 194]</span></p> + +<p>6. Examine the leaves of the worst weeds that you know of and see +if these will help in any way to account for their persistency.</p> +</div> + + +<h4 id="CH_VI_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>(1) In connection with Sections I and II, observe the effect of the lobing +and branching of leaves in letting the sunlight through. Notice any +general differences that may appear as to shape, margin, and texture in the +leaves of sun plants, shade plants, and water plants, and account for them. +Study the arrangement of leaves on stems of various kinds, with reference +to the size and shapes of leaves and their light relations. Consider the +value of the various kinds of foliage for shade; for ornament; as producers +of moisture; as food; as insect destroyers, etc.</p> + +<p>Make a special study of the twelve principal deciduous trees of your +neighborhood. Compare the leaves, bark, and branches of the same +trees so that you will be able to recognize them by any one of these means +alone.</p> + +<p>(2) In connection with Sections III and V, consider the effects upon soil +moisture of transpiration from the leaves of forest trees and from those +of shallow-rooted herbs and weeds that draw their water supply from +the surface. Consider the value of forests in protecting crops from excessive +evaporation by acting as wind breaks. Study the effect of the fall of +leaves upon the formation of soil. In any undisturbed forest tract turn up +a few inches of soil with a garden trowel and see what it is composed of. +Notice what kind of plants grow in it. Note the absence of weeds and +account for it. Compare the appearance of trees scattered along windy +hillsides, where the fallen leaves are constantly blown away, or in any +position where the soil is unrenewed, with those in an undisturbed forest, +and then give an opinion as to the wisdom of hauling away the leaves every +year from a timber lot.</p> + +<p>(3) In Section VII, observe, in different kinds of leaf mosaics, the means +by which the adjustment has been brought about and the purpose it subserves. +Make a list of plants illustrating the two habits. Notice the form +and position of petioles of different leaves, and their effect upon light exposure, +drainage, etc., and the behavior of the different kinds in the wind. +Look for compass plants in your neighborhood, and for other examples of +adjustment to heat and light. Study the position of leaves at different +times of day and in different kinds of weather and note what changes occur +and to what they are due.</p> + +<p>Make a list of ten plants that seem to you to have best worked out the +problem of leaf adjustment, giving the reasons for your opinion.</p> + +<p>Study the drainage system of different plants and observe whether there +is any general correspondence between the leaf drainage and the root systems.<span class="pagenum" id="Page_195">[Pg 195]</span> +This will lead to interesting questions in regard to irrigation and +manuring. Where plants are crowded, the growth of both roots and +leaves is complicated with so many other factors that it is best to select +for observations of this sort specimens growing in more or less isolated +situations.</p> + +<p>Notice the time of the expansion and shedding of the leaves of different +plants, and whether the early leafers, as a general thing, shed early or late; +in other words, whether there seems to be any general time relation between +the two acts of leaf expansion and leaf fall.</p> + +<p>(4) Under Section VIII, look for instances of modified leaves; study +the nature of the different modifications you find, and try to understand +their meaning and object. Make a collection (<i>a</i>) of all the leaves you can +find modified to serve other than their normal purposes; (<i>b</i>) of all the +organs of other kinds that have been modified to serve as leaves; (<i>c</i>) of +all the modified parts of leaves—stipules and petioles—that you can +find. Keep the collections separate, labeling each specimen with the +name of the plant it belongs to, what part it is, what use it serves, +when and where found. These collections need not be made individually, +but by the class as a whole and kept for the use of the school.</p> + +<p>Observe also (<i>d</i>) the differences between young and old leaves of the +same kind, and the leaves of young and old plants or parts of plants of the +same kind; (<i>e</i>) resemblances between young leaves belonging to plants of +different species; (<i>f</i>) between young leaves of one species and mature ones +of one or more different species. Make a collection of all the specimens you +can find illustrating the three points mentioned, referring each to its proper +head, and giving the name and relative age—old or young—of all specimens +collected.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_196">[Pg 196]</span></p> + +<h2 class="nobreak" id="CH_VII">CHAPTER VII. THE FLOWER</h2> +</div> + + +<h3 id="CH_VII_I">I. DISSECTION OF TYPES WITH SUPERIOR OVARY</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For monocotyls, any flower of the lily family, such as +tulip, dogtooth violet (<i>Erythronium</i>), trillium, star-of-Bethlehem, yucca, +bear’s grass, and the like. The large garden lilies make particularly good +examples, but they are for the most part spring bloomers. For autumn, +spiderwort (<i>Tradescantia</i>), arrow grass (<i>Sagittaria</i>), or late specimens of +colchicum and tiger lily may be used. Any of these will meet the essential +conditions of the analysis given in the text, but care should be taken not to +select for this exercise lily-like flowers of the iris and amaryllis families, +which have the <em>ovary inferior</em>.</p> + +<p>For examples of hypogynous dicotyls, flax, linden, pinks, corn cockle, +wood sorrel, poppies, tomato blossoms, and other common flowers can +usually be obtained without difficulty. In autumn, the geraniums so +largely cultivated for ornament will meet all the conditions of the analysis. +Specimens of the cress family—wallflower, cabbage, mustard, turnip—can +generally be found everywhere and at all seasons, and they possess +the advantage of having their flowers throughout the order put up on so +nearly the same pattern that a description of one species will answer, even +in details, for the rest.</p> + +<p>For sympetalous specimens of the hypogynous type, hyacinth, lily of +the valley, bearberry, huckleberry, or other equivalent forms may be +used.</p> + +<p><span class="smcap">Appliances.</span>—A compound microscope may be needed for examining +minute objects, such as pollen grains and ovules; but for all other purposes, +a good hand lens, with the pupil’s ordinary laboratory equipment +of drawing-materials, notebook, and dissecting needles, will be sufficient +for the studies outlined in this and the four succeeding sections.</p> +</div> + +<figure class="figcenter illowp90" id="i_207" style="max-width: 50em;"> + <img class="w100" src="images/i_207.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 265-267.</span>—Flower of a monocotyl (star-of-Bethlehem), with superior +ovary dissected: 265, entire flower, showing the different sets of organs: <i>pet</i>, +petals; <i>sep</i>, sepals; <i>sta</i>, stamens; <i>pist</i>, pistil; <i>ped</i>, peduncle; 266, side view with +all the petals and sepals but two removed to show order of the parts: <i>r</i>, receptacle; +<i>o</i>, ovary; <i>sty</i>, style; <i>stig</i>, stigma—parts composing the pistil; <i>f</i>, filament; +<i>a</i>, anther—parts composing the stamen; 267, cross section of the ovary: <i>c</i>, <i>c</i>, carpels; +<i>ov</i>, ovules; <i>pl</i>, placenta.</p></figcaption> +</figure> + +<p id="p-211"><b>211. The floral envelopes.</b>—Make a sketch of your +specimen flower from the outside. Is it solitary, or one of a +cluster? If the latter, refer to <a href="#p-160">160-162</a> and tell the nature +of the cluster. Notice the color; is it conspicuous enough +to attract attention or not? Can this have anything to do +with its clustered or solitary position? Label the head of +the peduncle that supports the flower, <em>receptacle</em>; the outer<span class="pagenum" id="Page_197">[Pg 197]</span> +greenish leaves, <em>sepals</em>; the inner, lighter-colored ones, +<em>petals</em>. The sepals taken together form the <em>calyx</em>, and the +petals, the <em>corolla</em>. Where the petals and sepals are all +separate and distinct, as in the tulip and the star-of-Bethlehem, +the corolla is said to be <em>polypetalous</em> and the calyx +<em>polysepalous</em>, words meaning, respectively, many-petaled +and many-sepaled. <em>Monopetalous</em> and <em>monosepalous</em>, or +<em>sympetalous</em> and <em>synsepalous</em>, are terms used to describe a +condition in which the petals or sepals are all united into +one, as in the morning-glory and lily of the valley. In many<span class="pagenum" id="Page_198">[Pg 198]</span> +flowers, there is little or no difference between the two sets of +organs. In such cases the calyx and corolla together are +called the <em>perianth</em>, but the distinction of parts is always +observed, the outer divisions being regarded as sepals, the +inner ones as petals. These two sets of organs constitute +the <em>floral envelopes</em>, and are not essential parts of the flower, +as it can fulfill its office of producing fruit and seed without +them. Note their number, mode of attachment to the +receptacle, and how they alternate with each other. Remove +one of the sepals and one of the petals, and notice any +differences between them as to size, shape, or color. Which is +most like a foliage leaf? Hold each up to the light and try +to make out the veining. Is it the same as that of the foliage +leaves? If a light-colored flower is used, examine a specimen +that has stood in coloring fluid. How many of each set are +there?</p> + +<figure class="figcenter illowp90" id="i_207a" style="max-width: 50em;"> + <img class="w100" src="images/i_207a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 268-269.</span>—Yucca blossom: 268, external view: <i>br</i>, bract; <i>pd</i>, peduncle; +<i>r</i>, receptacle; <i>s</i>, sepal; <i>pet</i>, petal; 269, vertical section: <i>ped</i>, peduncle; <i>br</i>, bract; +<i>r</i>, receptacle; <i>per</i>, perianth; <i>sta</i>, stamen; <i>o</i>, ovary; <i>sty</i>, style; <i>stg</i>, stigma. The +last three parts named compose the pistil.</p></figcaption> +</figure> + +<figure class="figright illowp35" id="i_208" style="max-width: 36.3125em;"> + <img class="w100" src="images/i_208.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 270-274.</span>—Stamens: 270, a +typical stamen with the terminal anther, +<i>b</i>, surmounting the filament, <i>a</i>, +and opening in the normal manner +down the outer side of each cell; 271, +stamen of tulip tree, with adnate extrorse +anther; 272, stamen of an evening +primrose (<i>Œnothera</i>) with versatile +anther; 273, stamen of pyrola, the +anther cells opening by chinks or pores +at the top; 274, stamen of a cranberry, +with the anther cells prolonged into a +tube and opening by a pore at the apex. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-212"><b>212. The essential organs.</b>—Next sketch the flower on +its inner face, labeling the appendages just within the petals, +<em>stamens</em>, and the central organ +within the ring of stamens, +<em>pistil</em>. These are called essential +<em>organs</em> because they are +necessary to the production of +fruit and seed. Note their +mode of insertion, three of the +stamens in a flower like the +star-of-Bethlehem alternating +with the petals, and the other +three with these and with the +lobes of the base of the pistil.</p> + +<p id="p-213"><b>213. The stamens.</b>—Notice +whether the stamens are +all alike, or whether there are +differences as to size, height, +shape, color, etc. Do these +differences, if there are any,<span class="pagenum" id="Page_199">[Pg 199]</span> +occur indiscriminately and without order, or in regular succession +between the alternating stamens? Examine one of +the little powdery yellow bodies at the tip of the stamens, +and see whether they face toward the pistil or away from it.</p> + +<p>Remove one of the stamens and sketch as it appears under +the lens, labeling the powdery yellow body at the top, +<em>anther</em>, and the stalklike body supporting it, <em>filament</em>. Usually +the filaments are threadlike, whence their name, but +sometimes, as in the star-of-Bethlehem, they are flattened +and look like altered petals. See if you can find such a one. +What would you infer from this fact as to the possible origin +of the stamens? (<a href="#p-100">100</a>.)</p> + +<figure class="figright illowp40" id="i_209" style="max-width: 39.25em;"> + <img class="w100" src="images/i_209.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 275-278.</span>—Forms of pollen: 275, +from <i>mimulus</i>; 276, star cucumber; 277 +wild balsam apple; 278, <i>hibiscus</i>. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p>Notice the two little sacs or pouches that compose the +anther, as to their shape and manner of opening, or dehiscing, +to discharge the powder +contained in them. This +powder is called <em>pollen</em>, and +will be seen under the lens +to consist of little yellow +grains. These are of different +shapes, colors, and sizes, +in different plants, and their surface often appears beautifully +grooved and striate when sufficiently magnified. Place some +of the pollen under the microscope and draw two of the +grains, with their markings. In the hibiscus and others of +the mallow family, they are large enough to be seen with a +hand lens.</p> + +<p id="p-214"><b>214. The pistil.</b>—Remove the stamens and sketch the +pistil as it stands on the receptacle. Label the round or +oval enlargement at the base, <em>ovary</em>, the threadlike appendage +rising from its center, <em>style</em>, and the tip end of the style, +<em>stigma</em>. In some specimens the style may be very short, or +wanting. In this case the stigma is <em>sessile</em>, and the pistil +consists of stigma and ovary alone. If the stigma is lobed +or parted, count the divisions and see if there is any correspondence +between them and the number of petals and sepals,<span class="pagenum" id="Page_200">[Pg 200]</span> +or of the lobes of the ovary. Examine the tip with a lens +and notice the sticky, mucilaginous exudation that moistens +it. Can you think of any use for this? If not, touch one of +the powdery anthers to it, and examine it again with a lens. +What do you see? Can you blow or dust the pollen from +the stigma?</p> + +<p id="p-215"><b>215. Pollination</b>, or the transfer of pollen from the anther +to the stigma, is a matter of great importance, as the pistil +cannot develop seed without it, except in the case of a few +plants like the Alpine everlasting, some species of meadow +rue (<i>Thalictrum</i>), and <i>Alchemilla</i>, which have the unusual +faculty of perfecting seeds in the absence of pollen. Note +the relative position of pistils and stamens and see if it is +such that the pollen can reach the stigma without external +agency.</p> + +<p id="p-216"><b>216. The ovary.</b>—Observe the shape of the ovary, and +the number of ridges, or grooves, that divide the surface. +Select a flower which has begun to +wither, so that the ovary is well +developed, cut a cross section near +the middle, and try to make out the +number of <em>locules</em>, or internal divisions. +Do you perceive any correspondence +in number between these +and the ridges or lobes outside (<a href="#i_210">Fig. +280</a>)? Between them and the lobes +of the stigma? The walls that +inclose the cavities of the ovary +are called <em>carpels</em>, and the ridges or +depressions that mark their point +of union on the outside are the +<em>sutures</em>, or seams. The little round +bodies in the locules, as the compartments of the ovary are +called, are the <em>ovules</em>, which will later be developed into seeds. +Their place of attachment is the <em>placenta</em>. If they are +attached to the walls of the carpels (<a href="#i_211">Fig. 281</a>), the placenta<span class="pagenum" id="Page_201">[Pg 201]</span> +is <em>parietal</em>; if to a central axis formed by the edges of the +carpels projecting inwards (<a href="#i_211">Fig. 282</a>), it is central and axial; +if instead of being attached to the carpels, the ovules are +borne on a projection from the receptacle, the placenta is a +<em>free central</em> one (<a href="#i_211">Fig. 283</a>). If your cross section shows a +central placenta, make +a vertical cut down to +the receptacle and find +out whether it is free, +or axial. What appears +to be the primary +office of the ovary? +Make an enlarged +sketch of your specimen +in both vertical and horizontal section, labeling correctly +all the parts observed.</p> + +<table class='wd90'> +<tr><td class='pr1'> +<figure class="figright illowp100" id="i_210" style="max-width: 27.375em;"> + <img class="w100" src="images/i_210.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 279, 280.</span>—Ovary of +yucca, a hypogynous monocotyl, +dissected: 279, vertical +section; <i>ov</i>, ovules; 280, diagram +of a horizontal section of the +same, enlarged, showing the +three carpels and six locules; +<i>ds</i>, dorsal sutures; <i>vs</i>, ventral +sutures; <i>ov</i>, ovules; <i>pl</i>, placenta.</p></figcaption> +</figure> +</td><td> +<figure class="figright illowp100" id="i_211" style="max-width: 50em;"> + <img class="w100" src="images/i_211.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 281-283.</span>—Different kinds of placenta: +281, parietal; 282, central and axial; 283, free +central. 281 and 282 are horizontal sections; 283, +vertical.</p></figcaption> +</figure></td></tr></table> + +<figure class="figright illowp25" id="i_211a" style="max-width: 20em;"> + <img class="w100" src="images/i_211a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 284.</span>—Horizontal +diagram of a +flower of the lily kind. +The dot represents the +growing axis of +the plant.</p></figcaption> +</figure> + +<p id="p-217"><b>217. Numerical plan.</b>—Make a horizontal diagram +of the plan of the whole flower, after the model given in +<a href="#i_211a">Fig. 284</a>, showing the order of attachment of the different +cycles,—sepals, petals, stamens, and pistils,—the number +of organs in each set, and their mode of alternation with the +organs of the other cycles. Notice that the +parts of each set are in threes, or multiples +of three. This is called the numerical plan +of the flower, and is the prevailing number +among monocotyls. It is expressed in botanical +language by saying that the flower is +<em>trimerous</em>, a word meaning measured, or +divided off, into parts for three.</p> + +<p id="p-218"><b>218. Vertical order.</b>—Next make a vertical +diagram of your specimen after the +manner shown in <a href="#i_207a">Fig. 269</a>, and note carefully that the ovary +stands <em>above</em> the other organs (this is true of all the lily +family), and is entirely separate and distinct from them. In +such cases the ovary is said to be <em>free</em>, or <em>superior</em>, and the +other organs <em>inferior</em>, or <em>hypogynous</em>, a word meaning “inserted<span class="pagenum" id="Page_202">[Pg 202]</span> +under the pistil.” These terms should be remembered, +as the distinction is an important one in plant evolution.</p> + +<p id="p-219"><b>219. Summary of observations.</b>—In the flower just examined, +we found that there were four sets of floral organs +present—sepals, petals, stamens, and pistil; that the individual +organs in each set were alike in size and shape; that +there were the same number, or multiples of the same +number of parts in each set, and that all the parts of each set +were entirely separate and disconnected, the one from the +other, and from those of the other cycles. Such a flower is +said to be:—</p> + +<p><em>Perfect</em>, that is, provided with both kinds of organs essential +to the production of seed—stamens and pistil.</p> + +<p><em>Complete</em>, having all the kinds of organs that a flower can +have: viz. two sets of essential organs, and two sets of +floral envelopes.</p> + +<p><em>Symmetrical</em>, having the same number of organs, or multiples +of the same number, in each set.</p> + +<p><em>Regular</em>, having all the parts of each set of the same size +and shape, as in the wild rose and bellflower, or if different, +arranged in regular order or pairs, so that there will be a +correspondence between the two sides of the flower, as in the +violet, sweet pea, sage, and larkspur. For convenience, the +two kinds may be distinguished as <em>complete</em> and <em>bilateral +regularity</em>, respectively.</p> + +<p>The opposites of these terms are: <em>imperfect</em>, <em>incomplete</em>, +<em>asymmetrical</em> or <em>unsymmetrical</em>, and <em>irregular</em>.</p> + +<p>Note that regularity refers to form, symmetry to number +of parts, and that a flower may be perfect without being +complete.</p> + +<figure class="figcenter illowp80" id="i_213" style="max-width: 50em;"> + <img class="w100" src="images/i_213.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 285-288.</span>—A flower of the cress family: 285, side view; 286, view from +above; 287, diagram of parts: <i>p</i>, petals; <i>s</i>, sepals; <i>st</i>, stamens; <i>pi</i>, pistil; <i>cl</i>, claw +of petal; +, +, position of the missing stamens; 288, pistil and stamens, enlarged. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_214" style="max-width: 37.625em;"> + <img class="w100" src="images/i_214.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 289.</span>—Section of a tomato flower, showing +the hypogynous arrangement: <i>cx</i>, calyx; +<i>c</i>, corolla; <i>s</i>, stamens; <i>p</i>, pistil; <i>o</i>, ovary; <i>st</i>, +stigma. (Twice natural size.)</p></figcaption> +</figure> + +<p id="p-220"><b>220. Dissection of a typical dicotyl flower.</b>—(Poppy, +flax, pink, tomato, linden, etc., can be substituted for the +specimen used in the text.) Gently remove the sepals and +petals from a wallflower, stock, mustard, or other cress +flower, lay them on the table before you in exactly the order +in which they grew on the stem, and sketch them. How<span class="pagenum" id="Page_203">[Pg 203]</span> +many of each are there, and how do they alternate with one +another? Sketch the pistil and stamens as they stand on +the receptacle; how many of the latter are there? Notice +that two of the six are outside and a little below the others, +alternate with the petals, while the other four stand opposite +them, as is natural, if they were alternating with another +ring of stamens between themselves and the corolla. Put a +dot before two of the sepals in your first drawing to indicate +the position of the two outer stamens, and a cross before +the other two to show where stamens are wanting to complete +the symmetry of this set, as in <a href="#i_213">Fig. 287</a>. When parts +necessary to complete the plan of a flower are wanting, as +in this case, they are said to be <em>obsolete</em>, <em>suppressed</em>, or +<em>aborted</em>. Place dots before the petals to represent the other +four stamens. Sketch one of the anthers as it appears +under a lens, showing the arrow-shaped base, and the +mode of attachment to the filament. Is it such that the +pollen can reach the stigma without external agency? In +what manner do the anthers open to discharge their pollen? +Are the anthers and stigma mature at the same time? +Remove all the stamens from a flower and sketch the pistil, +showing the long, slender ovary, the very short style, and the<span class="pagenum" id="Page_204">[Pg 204]</span> +<em>capitate</em> (that is, round and knoblike) stigma. Make cross +and vertical sections of one of the older pistils lower down +on the stem. How many +ovules does it contain? +How are they attached? +Represent the position +of the pistil by a small +circle in the center of +your sketch of the separate +parts. You have +now a complete ground +plan of the flower. Diagram +a vertical section, +as in <a href="#i_214">Fig. 289</a>, showing +the position of the ovary +with reference to the +other parts, and report +in your notebook as to the following points:—</p> + +<table class="autotable fs80"> +<tr> +<td class="tdl">Numerical plan</td> +<td class="tdl">Presence or absence of parts</td> +</tr> +<tr> +<td class="tdl">Symmetry</td> +<td class="tdl">Union of parts</td> +</tr> +<tr> +<td class="tdl">Regularity (complete or bilateral) </td> +<td class="tdl">Position of ovary</td> +</tr> +</table> + + +<h3 id="CH_VII_II">II. DISSECTION OF TYPES WITH INFERIOR OVARY</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For monocotyls: in spring and early summer, iris, snowflake, +freesia, crocus, narcissus, daffodil, can be used; in autumn, gladiolus, +blackberry lily, fall crocus, star grass (<i>Hypoxys</i>). For dicotyls: in spring, +flowers of apple, pear, quince, gooseberry, squash, gourd, melon (with both +male and female flowers); in late summer and autumn, fuchsia, evening +primrose (<i>Œnothera</i>), willow-herb (<i>Epilobium</i>).</p> +</div> + +<p id="p-221"><b>221. Study of a monocotyl flower.</b>—Compare with the +specimens examined in the last section, a narcissus, snowflake, +or iris flower. What difference do you notice in the +position of the ovary? Would you call it <em>inferior</em> (below the +other parts) or <em>superior</em> (above them)? How was it in the +lily and the hyacinth? If your specimen is an iris, notice +that it is sessile in the axil of a large bract called a <em>spathe</em>,<span class="pagenum" id="Page_205">[Pg 205]</span> +which conceals the lower part of the flower. Remove the +spathe and observe that the lower part of the perianth is +united into a long, narrow tube, from +the top of which the sepals and petals +extend as long, curving lobes.</p> + +<table> +<tr><td> +<figure class="figcenter illowp80" id="i_215" style="max-width: 20em;"> + <img class="w100" src="images/i_215.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 290.</span>—Iris flower: +<i>sp</i>, spathes; <i>s</i>, sepals + <i>p</i>, +petals = perianth.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_215a" style="max-width: 20em;"> + <img class="w100" src="images/i_215a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 291.</span>—Vertical +section of iris flower: +<i>ov</i>, ovules; <i>pl</i>, placenta; +<i>tu</i>, tube of the perianth +inclosing the style; <i>sta</i>, +stamen; <i>sti</i>, stigma: <i>o</i>, +ovary. (<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure></td></tr></table> + +<table> +<tr><td> +<figure class="figcenter illowp80" id="i_215b" style="max-width: 20em;"> + <img class="w100" src="images/i_215b.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 292.</span>—Vertical +section of iris flower, with +perianth removed, showing +a stamen and three stigmas: +<i>su</i>, stigmatic surface.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_215c" style="max-width: 21.25em;"> + <img class="w100" src="images/i_215c.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 293.</span>—Cross section +of ovary of iris flower: +<i>c</i>, <i>c</i>, carpels; <i>l</i>, <i>l</i>, locules; +<i>ov</i>, ovules; <i>pl</i>, placenta.</p></figcaption> +</figure></td></tr></table> + +<p id="p-222"><b>222. Arrangement of parts.</b>—Sketch +the outside +of the flower, +labeling the oblong, +three-lobed +enlargement at +the base, <em>ovary</em>; +the prolongation +above it, <em>tube of +the perianth</em>; the +three outer lobes +with the broad +sessile bases, +<em>sepals</em>; the others, +with their bases +narrowed and bent inward, <em>petals</em>. Now turn the flower over +and sketch the inside, labeling the three large, petal-like expansions +in the center, +<em>stigmas</em>. Do you +see any stamens? +Remove one of +the sepals and +look under the +stigma; what do +you find there? +Notice the little +honey pockets at +the foot of the +stamen. Run the +head of your pencil into them and see what would happen +to the head of an insect probing for honey.</p> + +<p><span class="pagenum" id="Page_206">[Pg 206]</span></p> + +<p>Remove the perianth and sketch the remaining organs in +profile, showing the position of the stamens. Do you see +any advantage in their position? Can you determine the +use of the crest of hairlike filaments on the upper side of the +sepals? Remove a stamen and sketch it.</p> + +<p id="p-223"><b>223. The pistil.</b>—Remove as much of the upper part of +the perianth tube as you can without injuring the pistil, +and with a sharp knife cut a vertical section down through +the ovary so as to show the long style and its connection with +the placenta. Make a sketch of this longitudinal section +(see <a href="#i_215a">Fig. 291</a>), labeling the parts observed. Notice whether +the placenta is central or parietal. Draw a cross section of +the ovary; how many locules has it? How many ovules in +each? Where are they attached? Is the placenta free +central or axial (<a href="#i_215c">Fig. 293</a>)? Examine with a lens the little +flap at the base of the two-cleft apex of one of the stigmas, and +look for a moist spot to which the pollen will adhere. Label +this in your sketch, <em>stigmatic surface</em>. No seeds can be matured +unless some of the pollen reaches this surface; can you +think by what agency it is carried there? What insects +have you seen hovering about the iris? Notice that in +drawing his head <em>out</em> of the flower, an insect would not +touch the stigmatic surface, since it is on the <em>upper</em> side of +the flap and he would be probing <em>under</em> it. But in entering +the next flower that he visits, he is likely to +strike his head against the flap and turn it +under, thus dusting it with pollen brought +from another flower.</p> + +<figure class="figright illowp25" id="i_216" style="max-width: 20em;"> + <img class="w100" src="images/i_216.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 294.</span>—Horizontal +diagram of iris +flower.</p></figcaption> +</figure> + +<p id="p-224"><b>224. Diagrams.</b>—Draw diagrams showing +the horizontal and vertical arrangement +of parts in the iris or other specimen examined, +and compare with those made of +the monocotyl studied in the preceding section. +In what respect does it differ from them? How do +you account for the difference in the number of stamens, if +there is any? (<a href="#p-220">220</a>.)</p> + +<p><span class="pagenum" id="Page_207">[Pg 207]</span></p> + +<p id="p-225"><b>225. The vertical order.</b>—The difference in vertical +arrangement is an important one. Bear in mind that flowers +of this type have the ovary <em>inferior</em>, that is, inserted <em>under</em> +the other organs (<a href="#i_217">Figs. 296</a>, <a href="#i_219a">304</a>), which are then said to be +superior, or <em>epigynous</em>, a word which, as you know from the +prefix <i>epi</i> <a href="#p-47">(47)</a>, means over or above the pistil. To make the +matter clear, the two sets of terms employed for describing +the position of the ovary are given below in parallel columns:</p> + +<table class="autotable fs80"> +<tr> +<td class="tdl">Hypogynous</td> +<td class="tdl">Epigynous</td> +</tr> +<tr> +<td class="tdl">Ovary superior</td> +<td class="tdl">Ovary inferior</td> +</tr> +<tr> +<td class="tdl">Calyx or perianth inferior</td> +<td class="tdl">Calyx or perianth superior</td> +</tr> +</table> + +<p>The epigynous arrangement is considered as marking a +higher stage of floral development than the hypogynous, +which is characteristic of a more +simple and primitive structure.</p> + +<figure class="figcenter illowp75" id="i_217" style="max-width: 50em;"> + <img class="w100" src="images/i_217.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 295-296.</span>—Evening primrose, dicotyl flower with inferior +ovary: 295, exterior view; 296, longitudinal section, +showing vertical arrangement of parts.</p></figcaption> +</figure> + +<p id="p-226"><b>226. Dissection of a dicotyl +flower.</b>—Sketch a blossom of +quince or apple, fuchsia, evening +primrose, etc., first from the outside, +then from the inside, and +then in vertical section, labeling +the parts as in +your other +sketches. Notice +in the pear +or apple how +the ovary is +sunk in the +hollowed-out +receptacle. +Where are the +other parts +attached? Are they inferior or superior? Hold up a petal +to the light and examine its venation through a lens. (Use +for this purpose a petal from a flower that has stood in red +ink for two or three hours.) Is it parallel-veined or net-veined?<span class="pagenum" id="Page_208">[Pg 208]</span> +If the flowers are clustered, what is the order of +inflorescence? Does the position of the flowers on their +branch correspond to that of +the leaf axils on the same +kind of plant?</p> + +<table> +<tr><td> +<figure class="figcenter illowp50" id="i_218" style="max-width: 39.0625em;"> + <img class="w100" src="images/i_218.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 297-300.</span>—Flower and sections +of pear: 297, cluster of blossoms, showing +inflorescence; 298, vertical section of a +flower; 299, ground plan of a flower; 300, +vertical section of fruit.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_219" style="max-width: 20em;"> + <img class="w100" src="images/i_219.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 301.</span>—Vertical +section of an almond +blossom with +petals removed, showing +the perigynous +arrangement.</p></figcaption> +</figure></td></tr></table> + +<p id="p-227"><b>227. The stamens.</b>—Remove +the petals from a flower +and examine the stamens +with a lens. Notice the attachment +and shape of the +anthers. Are they all of the +same color? How do you +account for the difference, if +there is any? Is the position +of the pistil and stamens +such that the pollen from +the anthers can readily reach +the stigmas without external +aid? Examine the pistil in +flowers of different ages, and +see if the stigma is mature (that is, moist and sticky) at the +same time that the anthers are discharging their pollen. +Make an enlarged sketch of a stamen showing the shape of +the anther and the method of opening to discharge pollen.</p> + +<p id="p-228"><b>228. The pistils.</b>—How many pistils do you find in the +apple blossom (or other flower under examination)? Are they +distinct, or united? Find where the styles originate; what +do you see there? Make a cross section of the ovary and +count the locules; how does their number compare with +that of the styles? Can you make out the number of ovules +in each? If not, use a young fruit; as it is only an enlarged +ovary, it will show the parts correctly. Compare it with a +ripe fruit and see if all the ovules matured. Can you think +of any reasons why some of them might fail? Do you see +any signs of nourishment stored in the ovary? Name all +the ways you can think of in which the ovary can benefit the<span class="pagenum" id="Page_209">[Pg 209]</span> +ovules and seeds. Draw the ovary in cross and vertical +sections, labeling correctly all the parts.</p> + +<figure class="figcenter illowp80" id="i_219a" style="max-width: 50em;"> + <img class="w100" src="images/i_219a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 302-304.</span>—Diagrams showing arrangement of parts with reference to the +ovary: <i>bd</i>, receptacle; <i>k</i>, calyx; <i>kr</i>, corolla; <i>st</i>, stamens; <i>fr</i>, ovary; <i>g</i>, style; <i>n</i>, +stigma; 302, perigynous; 303, hypogynous; 304, epigynous.</p></figcaption> +</figure> + +<p id="p-229"><b>229. The numerical plan of dicotyls.</b>—Diagram the plan +of the flower in cross and vertical section. How many parts +are there in each set? Can you tell readily +the number of stamens? When the individuals +of any set or cycle of organs are too +numerous to be easily counted, like the +stamens of the apple, pear, and peach, or +the petals of the water lily, they are said +to be <em>indefinite</em>. It is very seldom that perfect +symmetry is found in all parts of the +flower. The stamens and pistil, in particular, +show a great tendency to variation, so +that the numerical plan is generally determined +by the calyx and corolla. Where the +parts are in fives, as in the pear, quince, and wild rose, the +flower is said to be <em>pentamerous</em>, or in sets of five. This is the +prevailing number among dicotyls, though other orders are +not uncommon. In the mustard family <a href="#p-220">(220)</a> and other +well-known species, the fourfold order prevails, while some +of the saxifrages have their parts in twos, and the magnolia +and the pawpaw have a threefold arrangement.</p> + +<p><span class="pagenum" id="Page_210">[Pg 210]</span></p> + +<p id="p-230"><b>230. Intermediate types.</b>—Flowers like the peach and +rose represent an intermediate type in which the calyx, +petals, and stamens are attached to a prolongation of the +receptacle that extends above the ovary, but is not united +with it (<a href="#i_219">Fig. 301</a>). In general, a flower is not considered as +belonging to the epigynous kind unless the ovary is more or +less consolidated with the parts around it (<a href="#i_219a">Fig. 304</a>).</p> + + +<h3 id="CH_VII_III">III. STUDY OF A COMPOSITE FLOWER</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—The largest heads attainable should be selected, as the +florets are small at best, and difficult to handle. The large cultivated sunflower +(<i>Helianthus annuus</i>) makes an ideal specimen, if accessible. Oxeye +daisy and dandelion can be obtained throughout the season almost everywhere, +but the former has no pappus, and the latter does not show the +tubular disk flowers. Other common specimens are: for spring, mayweed, +Jerusalem artichoke, coreopsis, arnica; for late summer and autumn, +China aster, golden aster (<i>Chrysopsis</i>), sneezeweed, elecampane—and, +in fact, the great majority of flowers to be found at this season are of the +composite family. Oxeye daisy is used as a model in the text on account +of its general accessibility, but almost any specimen of the radiate kind +will meet all essential conditions of the analysis.</p> +</div> + +<figure class="figcenter illowp80" id="i_220" style="max-width: 53.75em;"> + <img class="w100" src="images/i_220.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 305-308.</span>—An oxeye daisy: 305, a flower head; +306, vertical section of a head; 307, disk flower; 308, ray +flower, enlarged.</p></figcaption> +</figure> + +<p id="p-231"><b>231. The ray flowers.</b>—Examine the upper side of an oxeye +daisy through a lens. Of what is the yellow button in the +center composed? Count the narrow, petal-like rays disposed +around +the center. To +decide what they +are, look for a +small two-cleft +body at the base +of the ray; this +is the pistil. +Do you see any +stamens in the +ray? An examination +will show +that all rays<span class="pagenum" id="Page_211">[Pg 211]</span> +contain pistils, but no stamens; they are, therefore, not petals, +but the corollas of imperfect flowers. Look at the upper edge +of a ray of sneezeweed, coreopsis, arnica, chicory, etc., for +small teeth or notches; these represent the lobes of a sympetalous +corolla. Split one of the tubular corollas of the disk +down one side and open it out flat; does it throw any light +on the morphology of the ray? In many composite plants, +as the sunflower, coneflower, coreopsis, the rays are all <em>neutral</em>; +that is, they have neither pistil nor stamens. Are they of any +use in such cases? If you are in doubt, remove all the rays +from a head; would the disk be noticeable enough to attract +attention without them? What is the principal office of +the rays?</p> + +<p id="p-232"><b>232. The involucre.</b>—Look at the cluster of green, leafy +scales on the under side of the head. It is not a calyx, but +a collection of bracts, called an <em>involucre</em>. Have you ever +noticed the bracts under the separate flowers on a raceme? +(<a href="#p-161">161</a>.) What would be the position of the bracts if all the +flowers of the raceme were compacted into a head like the +daisy or sunflower? Is the involucre of any use? Cut it +away gently so as not to disturb the other organs and see +what happens to the rays.</p> + +<p id="p-233"><b>233. The disk flowers.</b>—Cut a vertical section through +the head of a flower and notice the broad, flat receptacle (in +some cases round or columnar) on which the tiny florets +are seated. Observe whether it is naked, or whether it +bears chaffy scales inclosing the florets. Make an enlarged +drawing of this section, showing the insertion of the different +parts and labeling them all correctly. What differences +do you observe between the disk and the ray flowers?</p> + +<p id="p-234"><b>234. The pappus.</b>—Open one of the disk flowers with a +dissecting needle and observe the small striate (in some +specimens, hairy) body to which the base of the style is attached. +This is the ovary, inclosed in the lower part of the +calyx, which has become incorporated with it. When mature, +it will form a small, one-seeded fruit called an <em>akene</em>. Can<span class="pagenum" id="Page_212">[Pg 212]</span> +you see the ovule? Where is it attached? (Use a mature +akene for this purpose.) In most plants of this family, the +akene is surmounted by delicate hairy bristles, as in the +dandelion, wild lettuce, and groundsel; or by small chaffy +scales, as in the sneezeweed and sunflower, and sometimes +by hooks and barbed hairs, like those of the tickseed, bur +marigold, and cocklebur. These appendages constitute the +<em>pappus</em>. They are modifications +of the sepals, and serve an important +purpose in aiding the distribution +of the seed. Can you +suggest some of the ways in which they may aid in accomplishing +this object?</p> + +<figure class="figcenter illowp90" id="i_222" style="max-width: 50em;"> + <img class="w100" src="images/i_222.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 309-314.</span>—Akenes of the composite family: 309, mayweed (no +pappus); 310, chicory (pappus a shallow cup); 311, sunflower (pappus of two +deciduous scales); 312, sneezeweed (<i>Helenium</i>, pappus of five scales); 313, sow +thistle (pappus of delicate downy hairs); 314, dandelion, tapering below the +pappus into a long beak. (<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<figure class="figright illowp40" id="i_223" style="max-width: 50em;"> + <img class="w100" src="images/i_223.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 315-317.</span>—Flowers of <i>Arnica +montana</i>, showing successive stages in pollination: +315, pistil just extruding from +anther tube, covered with pollen, but with +stigmatic surfaces closed; 316, stigma +opened and mature; 317, stigma recurved +to receive pollen from its own or neighboring +anthers if foreign pollen has not +reached it.</p></figcaption> +</figure> + +<p id="p-235"><b>235. The stamens and pistil.</b>—Remove the corolla of a +disk flower carefully so as not to disturb the inclosed organs, +and notice how the stamens are united into a tube by their +anthers. Flatten out the tube and make an enlarged sketch +of it, showing the long, narrow shape of the anthers and their +mode of attachment. Can you make out how they open to +discharge their pollen? Examine one of the younger florets +near the center of the disk, and observe that the tip of the +style is inclosed in the anther tube with the lobes of the +stigma pressed tightly together by their inner faces (<a href="#i_223">Fig. 315</a>), +so that it is impossible for any of the pollen to reach the stigmatic<span class="pagenum" id="Page_213">[Pg 213]</span> +surface. It remains in this position till the anthers have +shed their pollen, then, as may be seen by examining an older +flower, the style begins to elongate, pushing up the pollen +that has fallen on the hairy outside of the closed stigma, and +forcing it out of the corolla tube, where it can be scattered +by insects among the other +flowers of the cluster. When +the pollen of its own floret +has been thus disposed of, the +stigma lobes open and curl +outward, ready to receive the +pollen from other flowers. +This arrangement is practically +universal among plants +of the composite family; can +you divine its object? It +will be shown later, that much +larger and stronger seeds are +produced when the pistil is +pollinated from a different +flower, or, better still, from a +different plant of the same +species; hence, you see what +a useful adaptation this is.</p> + +<p id="p-236"><b>236. Nature of a composite flower.</b>—It will be evident, +from the examination just made, that the daisy, dandelion, +sunflower, etc., are not single flowers, but compact heads +of small blossoms so closely united as to appear like a single +individual; hence they are said to be <em>composite</em>, or compound. +They are the most numerous and widely disseminated +of all plants, comprising one seventh of the entire +flowering vegetation of the globe, and are regarded by +botanists as representing the most advanced stage of floral +evolution. Can you point out some of the adaptations to +which their success in solving the problems of plant life is +due? (<a href="#p-164">164</a>.)</p> + +<p><span class="pagenum" id="Page_214">[Pg 214]</span></p> + + +<h3 id="CH_VII_IV">IV. SPECIALIZED FLOWERS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For spring and early summer: sweet pea, black locust, +wistaria, lupine, or any of the characteristic butterfly-shaped flowers of +the pea family. For autumn or late summer: tropæolum, monkshood, +or a bilabiate flower—snapdragon, digitalis, dead nettle, salvia, catalpa, +etc.—of the mint or figwort family.</p> +</div> + +<p id="p-237"><b>237. Irregularity and specialization.</b>—Irregularity and +bilateral regularity are, as a rule, indicative of specialization, +or adaptation to a particular purpose, such as the ready +distribution of pollen, or its protection against injury. These +adaptations are more noticeable in the corolla than in other +parts, and hence flowers of this kind are usually classed +according to the shape of their corollas. The most highly +specialized flowers in this respect are the orchids, but they +are too rare and difficult of access to be available objects for +study. The most familiar and widely distributed kinds of +specialized corollas are the <em>bilabiate</em>, or two-lipped, and the +<em>papilionaceous</em>, or butterfly, forms. The first is characteristic +of the mint and figwort families, of which the toadflax, +sage, and catalpa are familiar examples. The second comprises +the well-known papilionaceous flowers of the pea +family, named from the Latin word <i>papilio</i>, a butterfly, on +account of their general resemblance to that insect.</p> + +<p id="p-238"><b>238. Dissection of a papilionaceous flower.</b>—Sketch a +blossom of any kind of pea or vetch as it appears on the +outside. Are the sepals all of the same length and +shape? If not, which are the shorter, the upper or the +lower ones?</p> + +<p>Turn the flower over and examine its inner face. Notice +the large, round, and usually upright petal at the back, the +two smaller ones on each side, and the boat-shaped body +between them, formed of two small petals more or less united +at the apex. Press the side petals gently down with the +thumb and forefinger and notice how the essential organs are +forced out from the little boat in which they are concealed.<span class="pagenum" id="Page_215">[Pg 215]</span> +Observe how the end of the style is bent over so as to bring +the stigma uppermost when the petals are depressed. Imagine +the legs of a bee or a butterfly resting there as he probed +for honey; with what organ would his body first come in +contact when he alighted? If his thorax and abdomen had +previously become dusted with pollen when visiting another +flower, where would the pollen be deposited? Do you notice +anything in the color, shape, or odor of this flower that would +be likely to attract insects? Have you ever observed insects +hovering around flowers of this kind; for example, in clover +and pea fields, and about locust trees and wistaria vines? +What kind of insects, chiefly, have you seen about them?</p> + +<figure class="figcenter illowp90" id="i_225" style="max-width: 50em;"> + <img class="w100" src="images/i_225.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 318-322.</span>—Dissection of a papilionaceous flower: 318, front view of a +corolla; 319, the petals displayed: <i>v</i>, vexillum, or standard; <i>w</i>, wings; <i>k</i>, keel; +320, side view with all except one of the lower petals removed, showing the essential +organs protected in the keel: <i>l</i>, loose stamen; <i>st</i>, stamen tube; 321, side view, +showing how the anthers protrude when the keel is depressed; 322, ground plan. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p>Remove the sepals and petals from one side, and sketch +the flower in longitudinal section, showing the position of the +pistil and stamens. Then remove all the petals, and spread +in their natural order on the table before you, and sketch as +they lie (<a href="#i_225">Fig. 319</a>). Label the large, round upper one, +<em>standard</em> or <em>vexillum</em>; the smaller pair on each side, <em>wings</em>, +and the two more or less coherent ones in which the pistil +and stamens are contained, <em>keel</em>.</p> + +<p id="p-239"><b>239. The stamens.</b>—Count the stamens, and notice +how they are united into two sets of nine and one. Stamens<span class="pagenum" id="Page_216">[Pg 216]</span> +united in this way, no matter what the number in each set, +are said to be <em>diadelphous</em>, that is, in two brotherhoods. +Notice the position of the lone brother, whether below the +pistil—next to the keel—or above, facing the <em>vexillum</em>. +Would the projection of the pistil, when the wings are depressed, +be facilitated to the same extent if the opening in the +stamen tube were on the other side, or if the filaments were +<em>monadelphous</em>—all united into one set? Flatten out the +stamen tube, or sheath, formed by the united filaments, and +sketch it.</p> + +<p id="p-240"><b>240. The pistil.</b>—Remove all the parts from around the +pistil, and sketch it as it stands upon the receptacle. Look +through your lens for the stigmatic surface <a href="#p-223">(223)</a>. See if +there are any hairs on the style, and if so, whether they +are on the front, the back, or all around. Can you think of a +use for these hairs? Notice how the long, narrow ovary is +attached to the receptacle; is it sessile, or raised on a short +footstalk? If the latter, label the footstalk, <em>stipe</em>. Select a +well-developed pistil from one of the lower flowers, open the +ovary parallel with its flattened sides, and sketch the two +halves as they appear under the lens. Notice to which side +the ovules are attached, the upper (toward the vexillum) or +the lower, and label it, placenta. How many locules has the +ovary? How many carpels? How can you tell <a href="#p-216">(216)</a>?</p> + +<p id="p-241"><b>241. Plan of the flower.</b>—Diagram the flower in horizontal +and vertical section, and decide upon the following +points:—</p> + +<table class='autotable'> +<tr> +<td class='tdl'>Numerical plan</td> +</tr><tr> +<td class='tdl'>Symmetry</td> +</tr><tr> +<td class='tdl'>Regularity</td> +</tr><tr> +<td class='tdl'>Union of parts</td> +</tr><tr> +<td class='tdl'>Position of the ovary</td> +</tr></table> + +<figure class="figright illowp60" id="i_227" style="max-width: 50em;"> + <img class="w100" src="images/i_227.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 323, 324.</span>—Salvia: 323, a newly opened +flower, showing the pollen-covered anther striking +the back of a visiting bee; 324, an older flower, +with the protruding pistil rubbing against the back +of a bee covered with pollen from a younger flower.</p></figcaption> +</figure> + +<p id="p-242"><b>242. Significance of these distinctions.</b>—These distinctions +are important to remember, not only because they are +very useful in grouping and classifying plants, but because +they mark successive stages in the evolution of the flower. +In general, flowers of a primitive type and less advanced<span class="pagenum" id="Page_217">[Pg 217]</span> +organization are characterized by having their organs free +and hypogynous, while the more highly developed forms show +a tendency to consolidation and union of parts, and the +epigynous mode of +insertion. Irregularity +also, since it indicates +specialization +and adaptation to a +particular purpose, +may be regarded as a +mark of advanced +evolution.</p> + +<figure class="figcenter illowp80" id="i_227a" style="max-width: 50em;"> + <img class="w100" src="images/i_227a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 325, 326.</span>—Salvia: 325, longitudinal section through a flower, showing +the rocking connective which is struck at <i>a</i> by a visiting insect; 326, section of the +same flower after being visited, showing the lower arm of the connective pushed +back and lowering the anther.</p></figcaption> +</figure> + +<p id="p-243"><b>243. Dissection of +a bilabiate flower.</b>—Make +a similar study +of the flower of a +salvia, dead nettle, +catalpa, or other specimen +of the bilabiate +kind. Make diagrams +and report as to (1) numerical plan; (2) presence or absence +of parts; (3) regularity; (4) union of parts; (5) position of +ovary. Observe especially the relative position of stigma +and anthers; is it such that the pollen can reach the stigma +without external aid? Does the peculiar shape of the corolla +serve any other purpose than to attract the attention of<span class="pagenum" id="Page_218">[Pg 218]</span> +insect visitors by its conspicuous appearance? What is the +use of the projecting underlip? Is it any convenience to a +bee, for instance, to have a platform to rest on while gathering +pollen or honey? What is the use of the arched upper +lip? Cut it away and notice the exposed condition of the +stamens and pistil. Turn a flower upside down; what +would be the effect on a visiting bee or butterfly? (<a href="#exp-83">Exps. +83</a>, <a href="#exp-84">84</a>.)</p> + +<table> +<tr><td> +<figure class="figcenter illowp90" id="i_228" style="max-width: 30em;"> + <img class="w100" src="images/i_228.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 327.</span>—Staminodia, transformed +stamens of canna simulating +petals: <i>pet</i>, petals; <i>st</i>, +staminodia.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp50" id="i_228a" style="max-width: 20em;"> + <img class="w100" src="images/i_228a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 328.</span>—Flower +of a cactus +(<i>cereus greggii</i>), +showing transition +from scales to +petals.</p></figcaption> +</figure></td></tr></table> + +<p id="p-244"><b>244. Morphology of the flower.</b>—We have seen that the +venation of petals and sepals corresponds in a general way +with that of foliage leaves of the class to +which they belong, and that their arrangement +around their axis is analogous to the +arrangement of foliage leaves on the branch. +In our study of +inflorescence, it +was observed that +flowers and flower +buds occur in the +same positions +where leaf buds +occur, and that +they are subject +to the same laws +of arrangement +and growth. We +learned, also, in our study of leaves, something +about the wonderful modifications that +these organs are capable of undergoing; and +finally, an examination of a number of different flowers has +shown them capable of undergoing modifications to an equal +or even greater extent, and examples of the transition of +almost any floral organ into another may be observed by one +who will take the trouble to look for it. Stamens and petals +are found in all stages of transformation, from the slightly +flattened filament of the star-of-Bethlehem, or the yellow<span class="pagenum" id="Page_219">[Pg 219]</span> +pollen speck on the petal of a rose, to the brilliant staminodia, +or transformed stamens of the canna (<a href="#i_228">Fig. 327</a>), which simulate +petals so perfectly that their real nature is never suspected +by the ordinary observer. The transition from spines +and bracts to the brilliant corolla of the cactus (<a href="#i_228a">Fig. 328</a>) +is so gradual that we are hardly aware of it till we examine a +specimen and see it actually going on before our eyes.</p> + +<p>It must not be supposed, however, that an organ is ever +developed as one thing and then deliberately changed into +something else. When we speak loosely of one organ being +modified into another, the meaning is merely that it has developed +into one thing instead of into something else that it +was equally capable of developing into.</p> + +<p id="p-245"><b>245. The course of floral evolution.</b>—For the reasons +mentioned, the flower is regarded as merely a branch with +modified leaves and the internodes indefinitely shortened so +as to bring the successive cycles into close contact, the whole +being greatly altered and specialized to serve a particular +purpose. With this conception of the nature of the flower, +we can readily see that the less specialized its organs are and +the more nearly they approach in structure and arrangement +to the condition of an undifferentiated branch, the more +primitive and undeveloped is the type to which it belongs. +On the other hand, if the parts are highly specialized and +widely differentiated from the crude branch, a proportionately +high stage of floral evolution is indicated.</p> + + +<h3 id="CH_VII_V">V. FUNCTION AND WORK OF THE FLOWER</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For this exercise, flowers of the mallow family—hollyhock, +abutilon, mallow, hibiscus, cotton, okra, etc.—are particularly +recommended because they have pollen grains so large that they can be +studied fairly well with a hand lens. Lily, tulip, iris, etc., will also meet all +essential conditions of the study outlined in the text. A strand of silk +from a pollinated ear of corn is an excellent example for showing the +growth of the pollen tube, under the microscope.</p> + +<p><span class="smcap">Appliances.</span>—A compound microscope; a watch crystal; sugar solution +of 5 to 15 per cent.</p> + +<p><span class="pagenum" id="Page_220">[Pg 220]</span></p> + +<p id="exp-77"><span class="smcap">Experiment 77. To show the germination of pollen grains.</span>—Put +a drop of 5 per cent sugar solution into a watch crystal or a concave +slide, seal by smearing the edges with vaseline, and cover with a glass +to keep out the dust. Examine at intervals of five minutes under the +microscope (a hand lens will show the result with the specimens recommended, +though not so well), and the pollen grains will be observed to send +out long filaments or tubes into the sirup, as a germinating seedling sends +its radicle into the soil.</p> +</div> + +<p id="p-246"><b>246. Office of the flower.</b>—The one object of the flower +is the production of fruit and seed, and all its wonderful +specializations and variations of form and color tend either +directly or indirectly to this end.</p> + +<p id="p-247"><b>247. Pollination and fertilization.</b>—It was stated in <a href="#p-215">215</a> +that only in very exceptional cases can seed be developed +unless some of the pollen reaches the stigma. This act, +called <em>pollination</em>, is an essential step in seed production, but +is not sufficient to secure that end unless it leads to the process +known as <em>fertilization</em>. Successful pollination is a necessary +preliminary to fertilization, and the one begins where the +other ends.</p> + +<p id="p-248"><b>248. The next step toward fertilization.</b>—Examine with a +lens the pollinated pistil of a mallow, lily, or other large +flower, and notice the flabby, withered appearance of grains +that have stood for some time on the stigma, as compared +with those of a newly opened anther. Can you account +for the difference? Touch the tip of your tongue +to the stigma, or apply the proper chemical test, and it will +be seen that the sticky fluid which it exudes, contains sugar. +Refer to <a href="#exp-77">Exp. 77</a> and say what effect this substance has +on the pollen.</p> + +<figure class="figright illowp43" id="i_231" style="max-width: 25em;"> + <img class="w100" src="images/i_231.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 329.</span>—A +pollen grain emitting +a tube (magnified).</p></figcaption> +</figure> + +<p id="p-249"><b>249. The pollen tube.</b>—The same thing happens when a +pollen grain falls on the moist surface of the stigma. It +begins to germinate by sending a little tube down into the +substance of the pistil, and the withered appearance of the +grains on the stigma results from the nourishment in them +having been exhausted, just as the endosperm of the seed is +exhausted when the embryo begins to germinate. Here, however,<span class="pagenum" id="Page_221">[Pg 221]</span> +the analogy ends, for the pollen tube is not adapted, like +the radicle of the seedling, to absorb and convey nourishment +up to the other parts, but to feed and carry down to the ovary +two small bodies called <em>generative cells</em>, +which it discharges there, and then its work +is done and it disappears. So it must be +borne in mind that when we speak of the +germination of the pollen grains, we mean +something really very different from the +germination of a seed.</p> + +<p id="p-250"><b>250. The course of the pollen tube.</b>—Cut +the thinnest possible section through +a freshly pollinated pistil and place under +the microscope. Watch the pollen tubes +from the grains on the stigma as they descend +through the style toward the ovary. +A pollinated strand of corn silk—which is +only a very much elongated style—is excellent for this purpose. +It is so thin and transparent that no section need be +made, and the tube can be traced as it works its way down +through the entire length of the threadlike style to the young +grain, or ovary, on the cob. The time required for the tube +to penetrate to the ovary varies in different flowers according +to the distance traversed and the rate of growth. In the +crocus it takes from one to three days; in the spotted calla, +about five days; and in orchids, from ten to thirty days. +As a rule, it occupies only a few hours. Sometimes the pistil +is hollow, affording a free passage to the pollen tube; +in other cases, it is solid, and the growing tube eats its way +down, as it were, feeding on the substance of the pistil +as it grows. How is it in the flower you are examining? It +takes a grain of pollen to fertilize each ovule, and where more +than one seed is produced to a carpel, as is commonly the +case, at least as many pollen tubes must find their way to +each locule of the ovary as there are ovules—provided all +are fertilized.</p> + +<p><span class="pagenum" id="Page_222">[Pg 222]</span></p> + +<figure class="figright illowp40" id="i_232" style="max-width: 40em;"> + <img class="w100" src="images/i_232.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 330.</span>—Diagram of a simple +flower, showing course of the pollen +tube: <i>a</i>, transverse section of an +anther before its dehiscence; <i>b</i>, an +anther dehiscing longitudinally, with +pollen; <i>c</i>, filament; <i>d</i>, base of floral +leaves; <i>e</i>, nectaries; <i>f</i>, wall of carpels; +<i>g</i>, style; <i>h</i>, stigma; <i>i</i>, germinating +pollen grains; <i>m</i>, a pollen tube which +has reached and entered the micropyle +of the ovule; <i>n</i>, stalk of ovule; <i>o</i>, base +of the inverted ovule; <i>p</i>, outer +integument or testa; <i>q</i>, inner integument; +<i>t</i>, cavity of the embryo +sac; <i>u</i>, its basal portion; +<i>z</i>, oösphere.</p></figcaption> +</figure> + +<p id="p-251"><b>251. Fertilization.</b>—When a pollen tube has penetrated +to the ovary, it next enters one of the ovules, usually through +the micropyle (<a href="#i_232">Fig. 330</a>, <i>m</i>). +There it penetrates the wall of +a baglike inclosure called the +<em>embryo sac</em> (<a href="#i_232">Fig. 330</a>, <i>u</i>, <i>t</i>, <i>z</i>), +where one of the generative +cells emitted by the pollen tube +fuses with a large cell contained +in the embryo sac, known as +the <em>germ cell</em>, or <em>egg cell</em> (<a href="#i_232">Fig. +330</a>, <i>z</i>). The fusion of these +two bodies is what constitutes +fertilization. The cell formed +by their union finally develops +into the embryo, and the other +contents of the sac into the +endosperm, and the ripened +ovules become seeds.</p> + +<p id="p-252"><b>252. Stability of the process +of fertilization.</b>—The phenomena +that characterize the +functions of fertilization and +reproduction are the most uniform +and stable of all the life +processes, varying little not +only in different species and +orders, but throughout the whole vegetable kingdom. And +since these functions furnish a more reliable standard for +judging of the real affinities of the different groups than do +mere external resemblances, which are more liable to variation +and may often be accidental, they have been chosen +by botanists as the ultimate basis for the classification of +plants.</p> + +<p id="p-253"><b>253. Embryology.</b>—The study of the developing plantlet, +known as <em>embryology</em>, is a comparatively recent branch of<span class="pagenum" id="Page_223">[Pg 223]</span> +science, and has greatly enlarged our knowledge of the life +history of both plants and animals, by bringing to light resemblances +that exist between the most widely divergent +species in their earlier stages of development and thus +showing traces of a common origin. It has shown further, +that every individual plant or animal, in its development +from the embryo to the mature state, passes briefly through +stages apparently similar to those which the species has traversed +in the course of its evolution. This summary repetition, +by the individual, of the evolutionary progress of its +kind is known as the <em>biogenetic law</em>, and through its intelligent +application some of the most intricate problems in both +physiology and psychology have been solved.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Does the biogenetic law throw any light on the resemblances sometimes +observed between leaves of different ages in unlike species; for +example, the fig and the mulberry? (<a href="#p-170">170</a>; Field Work, <a href="#Page_195">p. 195</a>.)</p> + +<p>2. Can you name any other examples of plants or parts of plants which +show mutual resemblances in their early stages that do not exist at +maturity?</p> + +<p>3. Are there other causes than those acting under the biogenetic law +to which some of these resemblances may be referred; for instance, the +down and waxy coating on young leaves and bud scales? (<a href="#p-148">148</a>, <a href="#p-207">207</a>.)</p> +</div> + + +<h3 id="CH_VII_VI">VI. HYBRIDIZATION</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Several potted plants of tulip, lily, or any attainable +large flowered kind; or preferably a small plot in a garden or nursery.</p> + +<p><span class="smcap">Appliances.</span>—A pair of dissecting scissors, a camel’s-hair brush, and +some paper bags.</p> + +<p id="exp-78"><span class="smcap">Experiment 78. Does it make any difference whether a flower +has its ovules fertilized with its own pollen or with that of another +flower of the same kind?</span>—Carefully remove the <em>unopened</em> +anthers from a bud of a tulip, or other large flower just ready to unfold +(<a href="#i_234">Fig. 331</a>), inclose the mutilated bud in a small paper bag until the stigma +is mature, as shown by stickiness, then transfer to it with a camel’s-hair +brush some pollen from another flower. On the stigma of a second flower +of the same kind place some of its own pollen, and cover with a paper bag +until the stigma withers, to keep foreign pollen from reaching it by means<span class="pagenum" id="Page_224">[Pg 224]</span> +of wind or insects. Watch until seeds are matured. Which flower produces +the more seeds or the better ones? Plant the seeds; which produce +the more vigorous progeny?</p> + +<figure class="figcenter illowp90" id="i_234" style="max-width: 50em;"> + <img class="w100" src="images/i_234.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 331-333.</span>—Flower of Lorillard tomato: 331, newly opened bud, showing +stage in which the stamens should be removed; 332, mature flower: <i>cx</i>, calyx; <i>c</i>, +corolla; <i>s</i>, stamens; <i>st</i>, stigma; 333, flower with stamens removed for pollination. +(Natural size.)</p></figcaption> +</figure> + +<p id="exp-79"><span class="smcap">Experiment 79. Can a flower be fertilized with pollen of a +different kind?</span>—Dust the stigma of a tulip or a lily, from which the +stamens have been removed, with pollen from a narcissus, iris, or amaryllis. +Cover to protect from wind and insects. Are any seeds produced?</p> + +<p>Experiments of this kind, to be conclusive, ought to be performed on +a sufficient number of plants and through at least three generations. This +is hardly practicable for class work, but students who are specially interested +in the subject may carry on experiments at home, or supply their +place, to some extent, by observations out of doors, if there are any farms +or gardens accessible.</p> +</div> + +<figure class="figcenter illowp50" id="i_234a" style="max-width: 50em;"> + <img class="w100" src="images/i_234a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 334-335.</span>—Seeds of Bartlett pear, showing +the advantage of cross-fertilization: 334, cross-fertilized; +335, self-fertilized.</p></figcaption> +</figure> + +<p id="p-254"><b>254. Self-fertilization</b> +takes place +when a stigma is +pollinated from the +same flower. Horticulturists +have +long known that +continued self-fertilization, +or “in-breeding” +as it is +called by nurserymen, +tends to deteriorate +a stock; but<span class="pagenum" id="Page_225">[Pg 225]</span> +Charles Darwin was the first to explain, by a series of pains-taking +experiments, the meaning of those careful adjustments +which the more highly organized plants, as a rule, have developed +to guard against it.</p> + +<figure class="figcenter illowp75" id="i_235" style="max-width: 50em;"> + <img class="w100" src="images/i_235.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 336.</span>—Showing the effect of in-breeding on corn in one generation. The +two left-hand rows are from self-fertilized seed.</p></figcaption> +</figure> + +<p id="p-255"><b>255. Cross-fertilization</b> is effected by the pollination of a +stigma from another flower of the same variety or species. +As used by practical horticulturists, the expression means +that the two factors, pollen and ovule, belong to different +plants. Since pollination is the necessary antecedent to +fertilization, and the only means by which we can control it, +the breeder’s part in crossing is concerned with this act only +and nature does the rest. Darwin’s experiments—and they +are confirmed by the experience of plant growers everywhere—prove<span class="pagenum" id="Page_226">[Pg 226]</span> +that the offspring from crossing different plants of +the same kind is usually stronger and more productive than +that from self-fertilized ones; and if the parent stocks are +grown in different places and under different conditions, the +offspring is more vigorous than that from the same kind of +plants grown under like conditions. For instance, plants +from crossed seeds of morning-glory vines growing near each +other exceeded in height those from self-fertilized seeds as +100:76; while the offspring of plants growing under different +conditions exceeded those of the other cross, in height, as +100:78; in number of pods, as 100:57, and in weight of +pods, as 100:51. Knowledge of this kind, when applied to +the raising of fruits and grains for market, is of incalculable +value to gardeners and farmers, and also to the amateur who +raises fruits or flowers for pleasure.</p> + +<p id="p-256"><b>256. Hybridization</b> is the crossing of two plants of different +species or of widely separated varieties of the same species. +The resulting offspring is a <em>hybrid</em>. Hybridization can take +place only within certain limits. If the species are too unlike, +the pollen will either not take effect at all, or the resulting +offspring will be too weak and spindling to live; or if they +survive, will not be able to set seed (<a href="#exp-79">Exp. 79</a>).</p> + +<p><span class="pagenum" id="Page_227">[Pg 227]</span></p> + +<figure class="figcenter illowp45" id="i_237" style="max-width: 75em;"> + <img class="w100" src="images/i_237.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 11.</span>—Hybrid between a red and a white carnation, showing characters +intermediate between the two parents.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_228">[Pg 228]</span></p> + +<p id="p-257"><b>257. Effects of hybridization.</b>—The most important practical +uses of hybridizing are: (1) it “breaks the type” by +causing plants to vary, and thus gives the breeder a fresh +starting point for a new strain; and (2) when the parent +species are not too unlike, it accentuates the good effects of +crossing, and sometimes gives rise to offspring greatly surpassing +either parent in size and vigor. In regard to variability +it may act in three ways: (1) the hybrid may wholly +resemble one parent or the other, in which case there is, of +course, no variation; (2) it may resemble one parent more +than the other; or (3) it may show a blending of the characters +of the two, as when a cross between a red poppy and a +white gives rise to a light pink, or a mixed red and white +variety. In the first two cases, the characters of the parent +that manifest themselves are said to be <em>dominant</em>; those +which do not, <em>recessive</em>.</p> + +<figure class="figcenter illowp80" id="i_238" style="max-width: 50em;"> + <img class="w100" src="images/i_238.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 337.</span>—Effect of hybridization between related species in imparting superior +vigor to offspring: <i>M</i>, Californian black walnut (<i>Juglans californica</i>), male parent; +<i>F</i>, Eastern black walnut (<i>J. nigra</i>), female parent; <i>H</i>, hybrid.</p></figcaption> +</figure> + +<p id="p-258"><b>258. Mendel’s Law.</b>—So long ago as the middle of the last +century it was discovered by Gregor Mendel, an Austrian +investigator, that hybrids vary in certain cases according to +a fixed law, by means of which the proportionate share of the +characteristics of the two parent forms inherited by the offspring +can be foretold with almost mathematical precision. +The controversy over Darwin’s “Origin of Species,” which +was raging at the time, caused Mendel’s discoveries to be +overlooked for a generation, and it is only within the last +few years that their importance has been realized. The +principle of variation demonstrated by him in a series of +experiments, and confirmed by later investigators is, briefly,<span class="pagenum" id="Page_229">[Pg 229]</span> +this: If two parents differing in some fixed characteristic +be crossed, the entire offspring, in the first generation, will be +like the parent possessing the dominant quality. If all the +seed of this generation is planted and carefully protected +from foreign pollen, its offspring composing the second +generation from the parents will vary in the proportion of +¾ dominants (<i>D</i>, <i>D′</i>, line 2 of the diagram) to ¼ recessives (<i>R</i>). +Planting <em>all</em> the seeds of the second generation and carefully +shielding their progeny from foreign pollen, we get from <i>D</i>, +line 2, all pure dominants (<i>D</i>, line 3)—that is, plants producing +only their own type, and from <i>R</i>, line 2, all pure +recessives (<i>R</i>, line 3). But from each of the two sets of dominants, +<i>D′D′</i>, line 2, marked “impure” in the diagram, and +so called because their seeds may produce both dominants +and recessives, we get the same result as in the second generation, +namely: pure dominants (<i>D′D′</i>, line 3), pure recessives +(<i>R′R′</i>, line 3), and impure dominants (<i>D″D″</i>, <i>D″D″</i>, line +3). If it were possible to distinguish the seeds of these impure +dominants before germination and plant them only, for +no matter how many generations, the result would always be +approximately the same,—¼ pure dominants, ¼ pure recessives, +and ²⁄₄ impure dominants capable of producing both +dominants and recessives in the proportion of 3:1.</p> + +<figure class="figcenter illowp80" id="i_238a" style="max-width: 50em;"> + <img class="w100" src="images/i_238a.jpg" alt=""> + <figcaption><p class='center'>Diagram illustrating Mendel’s Law.</p></figcaption> +</figure> + +<p id="p-259"><b>259. Practical applications.</b>—Four principles of great +importance to plant breeders follow from this law in cases to +which it applies: (1) the absence of variation in the first +generation of hybrids is no sign that it may not occur later; +(2) pure recessives always breed true; hence, if they show +the desired character, no further selection is necessary for +that character; (3) pure dominants always breed true, but +the distinction between pure and impure is usually not +apparent in one generation; (4) the descendants of “impure” +parents cannot be depended upon to come true to +either type, but impure dominants may breed recessives, and +<i>vice versa</i>, with the presumption, however, of 3:1 in favor +of dominants.</p> + +<p><span class="pagenum" id="Page_230">[Pg 230]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Would hybridization account for some of the diversities mentioned +in <a href="#p-170">170</a>? (See <a href="#p-257">257</a>.)</p> + +<p>2. To what cases would it not apply? (<a href="#p-256">256</a>; <a href="#exp-79">Exp. 79</a>.)</p> + +<p>3. Would it be worth while to try to hybridize the potato and squash? +The squash and pumpkin? The lily and rose? Sweetbrier and wild +rose? Apple and peach? Wild crab and sweet apple? Blackberry and +strawberry? Blackberry and raspberry? Lemon and watermelon? +Lemon and orange? Why, or why not, in each case? (<a href="#p-256">256</a>; <a href="#exp-78">Exps. +78</a>, <a href="#exp-79">79</a>.)</p> +</div> + + +<h3 id="CH_VII_VII">VII. PLANT BREEDING</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—If practicable, visit a market garden, a florist’s establishment, +or, lacking these, the fruit and vegetable stalls of a city market.</p> +</div> + +<p id="p-260"><b>260. Fixing the type.</b>—It is the tendency of plants to +vary under the influence of climate, soil, food supply, crossing, +and other causes perhaps unknown to us, that makes +the plant breeder’s art possible. When a horticulturist sets +out to produce a new fruit or vegetable, he first forms in his +mind a clear idea of what he wants—whether increase of yield +or size, resistance to cold, drought, or disease, improvement in +flavor, color, shape, etc., or change in the time of maturing or +flowering (early and late varieties). Suppose, for instance, +he wishes to produce an oxeye daisy with all the disk florets +changed to white ones like the rays. He will begin by selecting +plants with the greatest number of rays and the most conspicuous +ones that he can find, and sowing the seeds of the flowers +which show the greatest tendency to the development of these +qualities. He will continue this process from generation to +generation, rigorously destroying all specimens that do not +approach nearer the ideal sought, until all disposition to +“rogue,” as the tendency to revert is called, has been eliminated. +When variations cease to occur and the seed of the +new variety always “come true,” the type is said to be <em>fixed</em>; +though some care will always be necessary to keep it so, +as the influence of changed surroundings and the danger of +mixture with foreign pollen must always be provided against.</p> + +<p><span class="pagenum" id="Page_231">[Pg 231]</span></p> + +<figure class="figright illowp50" id="i_241" style="max-width: 50em;"> + <img class="w100" src="images/i_241.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 338.</span>—A field of pumpkins grown from selected +seed.</p></figcaption> +</figure> + +<p id="p-261"><b>261. Survival of the fittest.</b>—In the fierce struggle +continually going on among both plants and animals for +food, shelter, and elbow room in the world, any individual +that happens to vary in a way which adapts it to +its surroundings a +little better than its +rivals, has an advantage +that will enable +it to survive when +less favored members +of the species +will perish. Its offspring, +or some of +them, may inherit +this quality and +transmit it, with the +attendant advantage, +to their posterity, +and so on, till +that particular +breed outstrips all +competitors, and in +time, as the less favored +intervening +forms die out, becomes +differentiated +as a new species. This is, in brief, the doctrine of natural +selection and the survival of the fittest.</p> + +<p id="p-262"><b>262. Artificial selection.</b>—Artificial selection enables the +breeder to accomplish more quickly what nature appears to +do by the slow process of natural selection. It is by this +means that our choicest fruits and vegetables have been developed +from greatly inferior, and sometimes inedible, wild +forms. Plants respond so readily to the influence of selection, +and the changes brought about by it are so rapid, +that new styles of fruits and flowers succeed each other in<span class="pagenum" id="Page_232">[Pg 232]</span> +the market with almost as great frequency and in as ready +response to demand as the new styles of women’s bonnets +and gowns in the shop windows.</p> + +<figure class="figcenter illowp80" id="i_242" style="max-width: 50em;"> + <img class="w100" src="images/i_242.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Fig. 339.</span>—Variation in blackberry leaves due to hybridization.</p></figcaption> +</figure> + +<p id="p-263"><b>263. Causes of variation.</b>—While man cannot directly +force plants to vary in any given direction, he can hasten the +process of variation by crossing, or by changing the conditions +under which they are growing. This is called “breaking +the type.” Hybridization furnishes the readiest means to +this end. Change of food supply, especially if accompanied +by excess of nourishment, is probably the expedient that +ranks next in effectiveness. Light, temperature, moisture, +character of the soil, exposure to wind, and the like, also +have their influence; and in adapting themselves to changes +in these various conditions, plants are apt to exhibit an +unusual number of variations, when removed from one locality +to another, especially if the difference in soil and climate +is very marked. Now comes the breeder’s opportunity. By +taking advantage of such variations as may occur either +spontaneously, or as the result of his efforts to break the type, +he will generally find some that will meet his requirements; +and knowing the effect produced by different conditions, he +can, to a certain extent, influence the course of variation in +the direction desired, by subjecting his specimens to the<span class="pagenum" id="Page_233">[Pg 233]</span> +conditions that tend to produce it. If he wishes to develop +a dwarf variety, for instance, he will take notice that overcrowding, +lack of nourishment, and cold tend to produce that +result in nature, and by acting on this hint he can direct his +efforts more intelligently. He will learn, too, not to waste +time in trying to breed a plant contrary to its nature. He +must not expect to gather figs from thistles by any art of +selection or skill in culture. By attention to Mendel’s law, +a still further saving of time and labor may be effected.</p> + +<p>It is obvious, from what has been said, that a breeder’s +chance of finding what he wants will be greater in proportion +to the number of individual plants he has to choose from. +For this reason, a horticulturist sometimes uses thousands +and hundreds of thousands of specimens of a single kind in +conducting his experiments. In this way he compresses into +a short space of time the advantage that nature can gain only +by spreading her random experiments over a long series of +years, or even centuries.</p> + +<figure class="figright illowp50" id="i_243" style="max-width: 50em;"> + <img class="w100" src="images/i_243.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 340.</span>—Mutation in twin ears of corn, +showing the sudden variations that sometimes +occur, by which a new type may be provided +without the labor of selection.</p></figcaption> +</figure> + +<p id="p-264"><b>264. Mutation and variation.</b>—There are at least two +ways in which changes in vegetable and animal forms are +thought to occur: (1) +by the preservation and +fixation through selection +and heredity, of +slight differences that +may appear from time to +time, such divergences +being called “fluctuating +variations”; (2) by +the appearance now and +then, due to causes as +yet unknown, of definite +and sudden changes +creating a new form at +a single, though perhaps small, leap. When such a change +is temporary and passes away with the individual in which<span class="pagenum" id="Page_234">[Pg 234]</span> +it first appeared, it is called a “sport,” and leads to no +important results; but when it is inherited by the offspring, +so that it is capable of giving rise to a new species, it constitutes +a “mutation.” The value of a mutation to breeders +in saving time and trouble is obvious. Professor Hugo de +Vries, a Dutch botanist, was the first to call attention to the +importance of mutation and its bearing upon the production +of new species.</p> + +<p id="p-265"><b>265. Factors in the evolution of species.</b>—Variation, +heredity, and selection are the three principal agents underlying +all changes, whether for the improvement or deterioration +of living organisms. The influence of external surroundings +in keeping up a variation once begun, or in starting new +ones, is also a factor that cannot be disregarded. It is for +this reason that natural species are so much more stable than +those brought about by man. The former, being evolved in +response to natural conditions, are liable to change only as +alterations in their surroundings are brought about by the +slow operation of natural causes. But the types resulting +from the breeder’s art, produced as they often are in response +to human demands and in direct opposition to the requirements +of natural conditions, are in a sense purely artificial, and +can be preserved only by keeping up the artificial surroundings +by which they were developed. Hence, the importance +of diligent cultivation and constant care and tillage, without +which the most carefully selected stocks may quickly “run +out” and degenerate into worthless forms.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Which are the more pliable to the breeder’s art, annuals or perennials? +Why? (<a href="#p-91">91</a>, <a href="#p-93">93</a>, <a href="#p-262">262</a>, <a href="#p-263">263</a>.)</p> + +<p>2. What advantage is gained by using buds and grafts instead of +seedlings in making new varieties of fruit trees? (<a href="#p-257">257</a>, <a href="#p-259">259</a>, <a href="#p-260">260</a>.)</p> + +<p>3. Would it be practicable to breed new varieties of slow-growing forest +trees, like oak, cypress, redwood, from seeds? Why or why not? (93, +<a href="#p-262">262</a>, <a href="#p-263">263</a>.)</p> + +<p>4. Can you account for the existence of the numerous intermediate +forms between the different species of oaks found in nature? (<a href="#p-255">255</a>, <a href="#p-257">257</a>.)</p> + +<p><span class="pagenum" id="Page_235">[Pg 235]</span></p> + +<p>5. If a breeder wished to produce a sweet-scented daisy or pansy, how +would he make his selections? (<a href="#p-260">260</a>.)</p> + +<p>6. Which would be the more useful for his purpose, a plant that showed +a general tendency to variability, or one that remained steadily fixed to +its type? (<a href="#p-260">260</a>.)</p> + +<p>7. What could he do to break the type? (<a href="#p-263">263</a>.)</p> + +<p>8. Would an intelligent breeder set out to produce edible roots and +tubers from wheat or barley? (<a href="#p-263">263</a>.)</p> + +<p>9. Would he think it worth while to try to develop a fleshy fruit from +a filbert or a walnut tree? From a haw? From sheepberry and black +haw? From tupelo (ogeechee lime)? (<a href="#p-263">263</a>.)</p> + +<p>10. Suppose a florist should wish to change the color of a rose from pink +to deep red; how could he hasten the process? (<a href="#p-257">257</a>, <a href="#p-263">263</a>.)</p> + +<p>11. Explain why it is so much easier to produce new varieties of plants +when there are already many kinds in existence, as, for example, the rose, +peach, and chrysanthemum. (<a href="#p-255">255</a>, <a href="#p-256">256</a>; <a href="#exp-78">Exps. 78</a>, <a href="#exp-79">79</a>.)</p> +</div> + + +<h3 id="CH_VII_VIII">VIII. ECOLOGY OF THE FLOWER</h3> + + +<h4 id="CH_VII_VIII_A">A. <span class="smcap">The Prevention of Self-pollination</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Any kind of unisexual flowers obtainable. Some good +examples for illustrating points mentioned in the text are: for spring and +early summer, catkins of almost any of our common forest trees,—oak, +hickory, willow, poplar, etc.; tassels and young ears of early corn; for +summer and early fall, flowers of late corn, and of melon, squash, pumpkin, +or others of the gourd family. Examples of <em>dichogamy</em> are: evening +primrose, showy primrose (<i>Œnothera speciosa</i>), willow herb (<i>Epilobium</i>), +dandelion, artichoke, sunflower, or any of the composite family; of <i>dimorphism</i>: +English primrose (<i>Primula</i>), loosestrife (<i>Pulmonaria</i>), bluets +(<i>Houstonia</i>), partridge berry; <i>cleistogamic</i>: fringed polygala, violets. +Peanuts, while not technically classed as cleistogamic, are strictly close-fertilized, +and approach the type so nearly that they may be used as an +illustration.</p> +</div> + +<p id="p-266"><b>266. Ecology</b> is the study of plants and animals in relation +to their surroundings. The principal modifications that +flowers undergo in this respect are in adapting themselves +for (1) pollination, and (2) protection.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp60" id="i_246" style="max-width: 28.8em;"> + <img class="w100" src="images/i_246.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 341, 342.</span>—Unisexual +flowers of willow: +341, staminate; +342, pistillate.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_246a" style="max-width: 39.1em;"> + <img class="w100" src="images/i_246a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 343.</span>—Twig of oak with +both kinds of flowers: <i>f</i>, fertile +flowers; <i>s</i>, <i>s</i>, staminate; <i>a</i>, pistillate +flower, enlarged; <i>b</i>, vertical +section of pistillate flower, +enlarged; <i>c</i>, portion of one of the +sterile aments, enlarged, showing +the clusters of stamens.</p></figcaption> +</figure></td></tr></table> + +<p id="p-267"><b>267. Unisexual flowers.</b>—The advantages of cross fertilization +were shown in the last two sections. It was also<span class="pagenum" id="Page_236">[Pg 236]</span> +shown that the first step taken by the breeder to secure this +result is to render the flower incapable of self-fertilization, +by removing the stamens. Nature accomplishes +the same purpose by the more +effectual expedient of providing imperfect, +or <em>unisexual</em> flowers, in which stamens +only, or pistils only, occur in the +same flower. When the stamens alone +are present, the flower is said to be staminate, +or <em>sterile</em>, because it is incapable +of producing seeds of its own, though its +pollen is a necessary factor in seed production. +If, on the other hand, the +ovary is present and the stamens absent, +the flower is pistillate and <em>fertile</em>; that is, capable of producing +fruit when impregnated with pollen. Sometimes both +stamens and pistils are wanting, as +in the showy corollas of the garden +“snowball,” the hydrangea, and +the rays of the sunflower. Such +blossoms are said to be <em>neutral</em>, +from the Latin word <i>neuter</i>, meaning +neither, because they have +neither pistils nor stamens. They +can, of course, have no direct part +in the production of fruit, but are +for show merely. (<a href="#p-231">231</a>.)</p> + +<p id="p-268"><b>268. Monœcious and diœcious +plants.</b>—When both kinds of +flowers, staminate and pistillate, +are borne on the same plant, as in +the oak, pine, hickory, and most of +our common forest trees, they are +said to be <em>monœcious</em>, a word which +means “belonging to one household”; when borne on separate +plants, as in the willow, sassafras, and black gum, they<span class="pagenum" id="Page_237">[Pg 237]</span> +are <em>diœcious</em>, or “of two households.” Draw a flowering twig +of oak, pine, or willow. Where are the fertile flowers situated? +Notice how very much more numerous the staminate flowers +are than the fertile ones. Why is this necessary? (<a href="#p-275">275</a>.)</p> + +<figure class="figcenter illowp60" id="i_247" style="max-width: 50em;"> + <img class="w100" src="images/i_247.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 344, 345.</span>—Flower of fireweed (<i>Epilobium angustifolium</i>): +344, with mature stamens and immature +pistil; 345, the same a few days older, with expanded +pistil after the anthers have shed their pollen. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-269"><b>269. Dichogamy</b> is the name applied to a condition where +the stamens and +pistils mature at +different times, +as in the evening +primrose, oxeye +daisy, and most +of the composite +family. It is a +very common +method in nature +for preventing +self-pollination, and quite as effective as the monœcious +arrangement, since it renders the flowers practically unisexual.</p> + +<figure class="figright illowp30" id="i_247a" style="max-width: 30em;"> + <img class="w100" src="images/i_247a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 346-347.</span>—Flower of pulmonaria: +346, long styled; 347, short +styled.</p></figcaption> +</figure> + +<p id="p-270"><b>270. Dimorphism</b> denotes a condition in which the stamens +and pistils are of different relative lengths in different +flowers of the same species, the stamens being long and the +pistils short in some, the pistils +long and the stamens short in +others. Flowers of this sort are +said to be <em>dimorphous</em>, or <em>dimorphic</em>, +that is, of two forms; and +some species are even <em>trimorphic</em>, +having the two sets of +organs long, short, and medium, +respectively, in different individuals. +Examples of dimorphic flowers are the pretty little +bluets (<i>Houstonia cœrulea</i>), the partridge berry, the swamp +loosestrife, and the English cowslip. Of trimorphic flowers +we have examples in the wood sorrel and the spiked loosestrife +(<i>Lythrum salicaria</i>) of the gardens. These flowers were a +great puzzle to botanists until the celebrated naturalist,<span class="pagenum" id="Page_238">[Pg 238]</span> +Charles Darwin, +proved by experiment +that the seeds +produced by pollinating +a dimorphous +flower with its own +pollen, or with pollen +from a flower of +similar form, are of +very inferior quality +to those produced +by impregnating a long-styled flower with pollen from a +short-styled one, and <i>vice versa</i>.</p> + +<figure class="figcenter illowp70" id="i_248" style="max-width: 50em;"> + <img class="w100" src="images/i_248.jpg" alt=""> + <figcaption><p class='center'><span class="smcap">Figs. 348-350.</span>—Three forms of loosestrife (<i>Lythrum +salicaria</i>).</p></figcaption> +</figure> + +<p id="p-271"><b>271. “Nature abhors self-fertilization.”</b>—These are the +three principal methods by which nature provides against +self-fertilization. Other cases occur in which the relative +position of the two organs is such that self-pollination is +difficult, or impossible, as in the iris and bear’s grass; or the +pollen may be incapable of acting on the stigma of the flower +that produced it. This aversion to self-fertilization is so +great that many flowers, even when capable of it, will give +preference to the pollen of another plant of the same +kind, if dusted with both. From his observations on the +behavior of plants in reference to this function, Charles Darwin +drew the conclusion that “Nature abhors perpetual +self-fertilization.”</p> + +<p id="p-272"><b>272. Cleistogamic flowers.</b>—Apparent exceptions to this +rule are the hidden flowers found on certain plants which +seem to have been constructed with a special view to self-fertilization. +They are called <i>cleistogamic</i>, or closed, because +they never open, but are fertilized in the bud; and those of +the fringed polygala do not even rise above ground at all. +Flowers of this kind can be found on several species of +violet, concealed under the leaves, close to the ground; and +the flowers of the peanut, found in the same situation, while +they open slightly, are close-fertilized and practically cleistogamic.<span class="pagenum" id="Page_239">[Pg 239]</span> +They are much more prolific than ordinary flowers, +but are not common, and seem to be a provision against +accident, for the plants producing them are generally provided +with other flowers of the usual kind,—some, as the +violet, having elaborate special adaptations for cross fertilization.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why does a strawberry bed sometimes fail to fruit well, although it +may flower abundantly? (<a href="#p-267">267</a>, <a href="#p-268">268</a>.)</p> + +<p>2. Are berries found on all sassafras trees? On all buckthorns? +Hollies?</p> + +<p>3. Would a solitary hop-vine produce fruit? A solitary ash tree? +(<a href="#p-267">267</a>.)</p> + +<p>4. Why is a mistletoe bough with berries on it so much harder to find +than one with foliage merely? (<a href="#p-267">267</a>, <a href="#p-268">268</a>.)</p> +</div> + + +<h4 id="CH_VII_VIII_B">B. <span class="smcap">Wind Pollination</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—In spring, catkins of forest trees, staminate and pistillate +flowers of pine. At nearly all seasons, heads of grain and panicles of various +kinds of grass can be obtained. For experiment, a potted plant of +any kind, just about to bloom, may be used.</p> + +<p id="exp-80"><span class="smcap">Experiment 80. To test the effect of shutting out external +agencies.</span>—Tie paper bags over flower buds of different kinds when nearly +ready to open and leave until the flowers have withered. On removing +the bags, mark with colored threads the flowers that had been covered, and +watch until seed time. Do you notice any difference in the number, size, +or weight of the seed produced by them and by those of the same kind left +exposed? How do you account for the difference, if there is any? By +what agencies could foreign pollen have been carried to the stigmas of +the exposed flowers? If any of the covered specimens wither and drop +their seed vessels without any attempt to fruit, examine a fresh flower, and +see if it is capable of self-pollination.</p> + +<p>As already explained, experiments of this kind, to be conclusive, should +be tried on as many specimens as possible. The greater the number of +species and individuals included, the better. Where it is not practicable +to carry on experiments by the class, pupils who are interested can make +them at home.</p> +</div> + +<p id="p-273"><b>273. The problem of pollination.</b>—When a plant has provided +against self-pollination, its problem is only half solved,<span class="pagenum" id="Page_240">[Pg 240]</span> +as it must now depend upon the conveyance of pollen to the +stigma by extraneous means.</p> + +<figure class="figright illowp40" id="i_250" style="max-width: 40em;"> + <img class="w100" src="images/i_250.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 351.</span>—Feathery stigmas of a grass +adapted to wind pollination.</p></figcaption> +</figure> + +<p id="p-274"><b>274. Adaptations to wind pollination.</b>—A very large +number of plants, among which are included nearly all our +principal forest trees, grains, +and grasses of every kind, +depend exclusively upon the +wind for the distribution of +their pollen. This being +the case, it is, of course, an +advantage to them to get +rid of all unnecessary appendages +that might hinder +a free play of the wind +among their flowers, and so +they consist, as a rule, of +essential organs only (<a href="#i_246">Figs. +341, 342</a>). Such flowers are +often distinguished, however, +especially among +grasses and low herbs, by +large, feathery stigmas that +are well adapted to catch and hold any stray pollen grains +which may be floating in the air. Place a stigma of oat or +other grass under the microscope and you will probably see +a number of pollen grains clinging to its branches.</p> + +<p id="p-275"><b>275. The disadvantages of wind pollination.</b>—This is a +very clumsy and wasteful method, however, for so much +pollen is lost by the haphazard mode of distribution that the +plant is forced to spend its energies in producing a vast +amount more than is actually needed, and great masses of it +are frequently seen in spring floating like patches of sulphur +on ponds and streams in the neighborhood of pine thickets. +Like those that are self-pollinated, wind-pollinated flowers +are generally very inconspicuous, devoid of odor, and of all +attractions of form or color, because they have no need of<span class="pagenum" id="Page_241">[Pg 241]</span> +these allurements to attract the visits of insects. Besides +being wasteful, wind pollination is very uncertain. The +pollen cannot be blown about very well unless it is dry, and +in rainy weather it may all be rotted or washed away before +it can reach the stigmas that are ready to receive it.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why do the flowers of oak, willow, and other wind-fertilized plants +generally appear before the leaves? (<a href="#p-274">274</a>.)</p> + +<p>2. Can you account for the showers of “sulphur” sometimes reported +in the newspapers? (<a href="#p-275">275</a>.)</p> + +<p>3. Do you see any connection between the feathery stigmas of most +grasses and their mode of pollination? (<a href="#p-274">274</a>.)</p> + +<p>4. Why are house plants not apt to seed so well as those left in the +open? (<a href="#exp-80">Exp. 80</a>.)</p> + +<p>5. Why are the tassels of corn placed at the tip of the stalk? (<a href="#p-274">274</a>.)</p> + +<p>6. Can you trace any connection between the winds and the corn crop? +(<a href="#p-274">274</a>.)</p> + +<p>7. If March winds should cease to blow, would vegetation be affected +in any way? (<a href="#p-274">274</a>.)</p> + +<p>8. Why are wind-fertilized plants generally trees or tall herbs? (<a href="#p-274">274</a>.)</p> + +<p>9. Is it good husbandry to plant different varieties of corn or other +grain in the same field, if it is desired to keep the strain pure? (<a href="#p-255">255</a>, <a href="#p-274">274</a>.)</p> + +<p>10. Is water a good pollen carrier? (<a href="#p-275">275</a>.)</p> + +<p>11. What is the only class of plants it is likely to reach?</p> + +<p>12. What is the only other agency, besides wind and water, by which +this office can be performed?</p> +</div> + + +<h4 id="CH_VII_VIII_C">C. <span class="smcap">Insect Pollination</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Half a dozen panes of glass, about 6 × 9; squares of +bright-colored cloth or paper; a few spoonfuls of honey or sirup; perfumes +of various kinds, preferably flower extracts; fetid and disagreeable +smelling substances, such as a bit of decaying animal or vegetable matter. +Observations on living plants can best be made out of doors or in a greenhouse, +as opportunity offers.</p> + +<p id="exp-81"><span class="smcap">Experiment 81. Has the color of flowers any attraction for +insects?</span>—Place half a dozen panes of ordinary window glass out of doors +or in an open window to which insects can have free access. Lay under +the first pane a piece of black paper or cloth, and under the others bright-colored +pieces of red, blue, white, yellow, and purple. Drop on the center +of each pane a little honey or sirup, and watch. Do insects show any +color preferences? Which color attracts fewest visitors? Which most?</p> + +<p><span class="pagenum" id="Page_242">[Pg 242]</span></p> + +<p id="exp-82"><span class="smcap">Experiment 82. Does odor influence insects?</span>—Try the same +experiment with different odors, removing the bright colors and sprinkling +some kind of perfume on each pane. Try also the effect of decaying +meat and other malodorous substances. Are any insects attracted by +these? What kinds? Does this account for the noisome smells of the +“carrion-flower” and skunk cabbage? What kinds of insects are attracted +by sweet-smelling substances? Do the greater number appear to be attracted +by these, or by foul odors? Are flowers of the sweet-smelling +or the foul-smelling kind more common in nature? Do insects seem to +be more strongly influenced by colors or by odors?</p> +</div> + +<p id="p-276"><b>276. The color of flowers</b>, being an adaptation to changing +external conditions, is a very unstable quality, and varies +greatly within the limits of the same species. Even on the +same stem, flowers of different colors are often found, due, +probably, to hybridization. Yet, notwithstanding all this +apparently random intermingling of hues, the range of color +for each species is confined, approximately, within certain +limits. Nobody has ever seen a blue rose or a yellow aster; +and though the florist’s art is constantly narrowing the application +of this law, it still remains true that in a state of +nature, certain colors seem to be associated together in the +floral art gamut. Yellow is considered the simplest and +most primitive color in flowers, and blue the latest and +most highly evolved. Yellow, white, and purple, in the +order named, are the commonest flower colors in nature; +blue, the rarest. Do you see any relation between these facts +and the color preferences of insects?</p> + +<p id="p-277"><b>277. Advantages of insect pollination.</b>—It is evident that +this is a much more certain as well as a more economical +method of securing pollination than through the haphazard +agency of wind or water. In probing around for the nectar +or the pollen upon which they feed, these busy little creatures +get themselves dusted with the fertilizing powder, which they +unconsciously convey from the stamen of one flower to the +pistil of another. Insects usually confine themselves, as far +as possible, to the same species during their day’s work, and +since less pollen is wasted in this way than would be done by<span class="pagenum" id="Page_243">[Pg 243]</span> +the wind, it is clearly to the advantage of a plant to attract +such visitors, even at the expense of a little honey, or of a +liberal toll out of the pollen they distribute.</p> + +<p id="p-278"><b>278. Special partnerships.</b>—Some plants have adapted +themselves to the visits of one particular kind of insect so +completely that they would die out if that +species were to become extinct. The well-known +alliance between red clover and the +bumblebee was brought to light when the +plant was first introduced into Australia. +It grew luxuriantly and blossomed profusely, +but would never set seed till the +bumblebee was introduced to +keep it company.</p> + +<table class='autotable'> +<tr> +<td> +<figure class="figcenter illowp70" id="i_253" style="max-width: 20em;"> + <img class="w100" src="images/i_253.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 352.</span>—Pod +of <i>yucca</i> pierced by +the <i>Pronuba yuccasella</i>.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp70" id="i_253a" style="max-width: 15em;"> + <img class="w100" src="images/i_253a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 353.</span>—Pronuba +pollinating +pistil of +yucca.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp70" id="i_253b" style="max-width: 30em;"> + <img class="w100" src="images/i_253b.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 354.</span>—Moth resting on yucca +blossom.</p></figcaption> +</figure></td></tr></table> + +<p>A remarkable partnership of +this kind exists between the +<i>pronuba</i>, or yucca moth, and +the flowering yuccas, of which the bear’s grass +and Spanish bayonet are familiar examples. +The pods of these plants are never perfect, but +all show a constriction at or near the middle, +such as is sometimes +seen in +the sides of +wormy plums +and pears. +This is caused by the larvæ +of the moth, which feed upon +the unripe seeds. A glance +under the nodding perianth +of a yucca blossom (<a href="#i_253b">Fig. 354</a>) +will show that the short stamens are curved back from the +pistil in such a manner that, under ordinary circumstances, +the pollen cannot reach the stigma except by the rarest +accident. But the yucca moth, as soon as she has deposited +her eggs in the seed vessel, takes care to provide a crop of<span class="pagenum" id="Page_244">[Pg 244]</span> +food for her offspring by gathering a ball of pollen in her +antennæ and deliberately plastering it over the stigma (<a href="#i_253a">Fig. +353</a>). In this way fertilization of the ovules and maturing +of the fruit is secured. The larvæ feed on the unripe seeds +for a time, but so few are +destroyed in proportion to +the number matured that +the plant can well afford to +pay the small toll charged +in return for the service +rendered.</p> + +<table class='autotable'> +<tr><td class='wd60'> +<figure class="figcenter illowp70" id="i_254" style="max-width: 50em;"> + <img class="w100" src="images/i_254.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 355.</span>—Upper boughs of a caprifig +tree, showing an abundant crop of +spring fruit.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp70" id="i_254a" style="max-width: 30em;"> + <img class="w100" src="images/i_254a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 356.</span>—Female wasps +issuing from the galls of caprifigs, +in which the eggs are +laid.</p></figcaption> +</figure></td></tr></table> + +<p id="p-279"><b>279. Caprification of the +fig.</b>—A more complicated +case of specialization is that +of the Smyrna fig of commerce—the +only one of the +species that is capable of +perfecting seeds. The +staminate flowers are borne on a separate tree, the caprifig, +which grows wild in the countries bordering on the Mediterranean. +The caprifigs, as the fruit of this tree is called, +are worthless except as the breeding +and nesting places of a small insect, +the fig wasp. This insect is the +necessary agent in conveying pollen +from the stamens of the caprifig to +the pistils of the Smyrna fig, which it +penetrates at certain seasons of the +year in the effort to lay its eggs. In +order to insure <em>caprification</em>, as this process is called, the +caprifigs are strung by hand on fillets of cord or raffia and +hung about on the trees which are to be fertilized. In this +case we have an example of a threefold partnership between +man, the fig tree, and the wasp, which is necessary to the +existence of two of the parties.</p> + +<p><span class="pagenum" id="Page_245">[Pg 245]</span></p> + + +<h4 id="CH_VII_VIII_D">D. <span class="smcap">Protective Adaptation</span></h4> + +<div class="blockquot"> + +<p id="exp-83"><span class="smcap">Experiment 83. Are the floral envelopes of any use?</span>—Carefully +remove the calyx and corolla from a young flower bud on a growing +plant and see what will happen. Remove them from a flower just unfolding. +Mark each by tying a colored thread lightly around the petiole and +see if it sets as many seeds, or as good ones, as the unmutilated flowers on +the same plant.</p> + +<p id="exp-84"><span class="smcap">Experiment 84. Is the position of a flower on the stem of any +importance?</span>—Invert a blossom of pea or sage, and see what parts would +come in contact with the body of a visiting insect. How would its chances +for pollination be affected? Try to make a flower grow in an inverted +position by tying or weighting it down, and watch the effect on seed production.</p> + +<p id="exp-85"><span class="smcap">Experiment 85. Is the position of flowers on the stem influenced +by light?</span>—Place a potted plant with expanding flower buds near a +window so that the light will reach it from one side only, and notice the +position of the buds. After a day or two reverse the position with regard +to light, and watch whether any change of position takes place.</p> +</div> + +<figure class="figcenter illowp90" id="i_255" style="max-width: 50em;"> + <img class="w100" src="images/i_255.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 357-359.</span>—Flower of monkshood, showing the changes by which it returns +to its original position under the influence of geotropism after the axis of inflorescence, +s, has been inverted: 357, inverted position; 358, change due to negative geotropism; +359, change due to lateral geotropism.</p></figcaption> +</figure> + +<div class="blockquot"> + +<p id="exp-86"><span class="smcap">Experiment 86. Is the position of flowers on the stem influenced +by geotropism?</span>—Lay a potted plant of lily of the valley, larkspur, +gladiolus, or digitalis in a horizontal position, tie the main stem to keep +it from changing its direction of growth, and leave for two or three days +in a place where it is lighted equally on all sides. How do the individual +flowers behave? What part bends to turn them up? Vary the experiment<span class="pagenum" id="Page_246">[Pg 246]</span> +by turning the pot bottom upwards so that the flowering axis will +point downwards. This can be done by inclosing the pot in a bag of strong +cheesecloth, with the string tied loosely but firmly around the foot of the +stem to prevent the contents from falling out, and suspending the whole +bottom upwards. In making these experiments, use flowers that grow +in a long cluster, or raceme, and hold the main axis in a vertical position +by tying or weighting it down. Watch the behavior of the individual +flowers. Arrange another pot containing the same kind of plant, in the +same way, and suspend one +in a dark place, keeping the +other in the light. Does the +same movement take place in +both? Is it in response to +light, or to gravity?</p> +</div> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp80" id="i_256" style="max-width: 40em;"> + <img class="w100" src="images/i_256.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 360, 361.</span>—Protection of pollen in the +thistle: 360, position at night, or during wet +weather; 361, position in sunshine.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_256a" style="max-width: 40em;"> + <img class="w100" src="images/i_256a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 362, 363.</span>—A bell flower: 362, position +in daylight; 363, position at night, or during wet +weather.</p></figcaption> +</figure></td></tr></table> + +<p id="p-280"><b>280. Means of protection.</b>—Where +plants +have adapted themselves +to insect pollination, +it is, of course, important to shut out intruders that +would not make good carriers. In general, small, creeping +things, like ants and +plant lice, are not such +efficient pollen bearers +as winged insects, and +hence the various devices, +such as hairs, +scales, and constrictions, +at the throat of +the corolla, by means +of which their access to +the pollen is prohibited. +To this class of adaptations +belong the hairy +filaments of the spiderwort, +the sticky ring +about the peduncles of +the catchfly, the swollen lips of the snapdragon, the scales or +hairs in the throat of the hound’s-tongue, the velvet petals<span class="pagenum" id="Page_247">[Pg 247]</span> +of the partridge berry, and the recurved edges of corollas +like those of the morning-glory and tobacco, over which small +crawling insects cannot easily climb.</p> + +<p>Of flowers that are pollinated by night moths, some close +during the day, as the four-o’clock and the evening primrose; +and <i>vice versa</i>, the morning-glory, dandelion, and dayflower +(<i>Commelyna</i>) unfold their beauties only in the sunlight. +For similar reasons, night-blooming flowers are generally +white or very light-colored, and shed their fragrance only after +sunset. A nodding position is assumed by many flowers at +night, or during a +shower, to keep the +pollen from being injured +by dew or rain.</p> + +<figure class="figcenter illowp80" id="i_257" style="max-width: 40em;"> + <img class="w100" src="images/i_257.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 364.</span>—A flower of the trumpet vine (<i>Tecoma +radicans</i>) adapted to pollination by humming birds +and humming bird moths, which has been pierced by +a bee or bird for honey.</p></figcaption> +</figure> + +<figure class="figcenter illowp80" id="i_257a" style="max-width: 40em;"> + <img class="w100" src="images/i_257a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 365.</span>—Head of the swordbill, a bird +adapted to feeding on nectar from long, +tubular corollas.</p></figcaption> +</figure> + +<p id="p-281"><b>281. Insect depredators.</b>—The +secretion +of honey is a +common means of +attracting insects, +and various adaptations, +such as spurs, sacs, and pockets, are provided for protecting +it against unwelcome intruders. In general, plants +that have long, tubular +flowers, like the trumpet +honeysuckle (<i>Lonicera sempervirens</i>) +and the trumpet +vine, are reserving their +sweets for humming birds, +or long-tongued moths and butterflies. This protective +device is not always successful, however, against insect depredators, +for it is not uncommon to find such corollas with +a puncture near the base, made by wasps or bees, and sometimes +by humming birds themselves, in their impatience to +get at the feast before the flower is open. Through the breach +thus made, a rabble of petty thieves can then find entrance.</p> + +<p><span class="pagenum" id="Page_248">[Pg 248]</span></p> + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Of what use is the brilliant coloring of the camellia? The large +flowers of the magnolia? The perfume of the rose and the violet? The +fetid odor of the ailanthus? (<a href="#p-277">277</a>; <a href="#exp-81">Exps. 81</a>, <a href="#exp-82">82</a>.)</p> + +<p>2. Are the tastes of insects in regard to odors always the same as ours? +(<a href="#exp-82">Exp. 82</a>.)</p> + +<p>3. Have flowers any economic value except for decorative purposes?</p> + +<p>4. Can you name any that are used as food or beverages? Any that +furnish spices and flavorings? Drugs, medicines, or dyes?</p> + +<p>5. What commercial food product is obtained almost entirely from +flowers?</p> + +<p>6. Name some of the flowers that are most valued by the beekeeper.</p> + +<p>7. Mention another important industry that is entirely dependent on +flowers.</p> + +<p>8. Name some of the flowers that are most important to the perfumer.</p> + +<p>9. Why do the seeds of fruit trees so seldom produce offspring true +to the stock? (<a href="#p-256">256</a>, <a href="#p-257">257</a>, <a href="#p-271">271</a>, <a href="#p-277">277</a>.)</p> + +<p>10. Would you place a beehive near a field of buckwheat? Of clover? +Near a strawberry bed? In a peach orchard? Near a fig tree? Under +a grape arbor?</p> + +<p>11. Why are very conspicuous flowers, like the camellia, hollyhock, and +pelargoniums, so frequently without odor?</p> + +<p>12. Why is the wallflower “sweetest by night”? (<a href="#p-280">280</a>.)</p> + +<p>13. What advantage can flowers like the morning-glory gain by their +early closing? (<a href="#p-280">280</a>.)</p> + +<p>14. Of what use to the cotton plant, Japan honeysuckle, and hibiscus +is the change of color their blossoms undergo a few hours after opening? +(<a href="#p-277">277</a>, <a href="#p-278">278</a>, <a href="#p-280">280</a>.)</p> + +<p>15. Why does the Japan honeysuckle, which has run wild so abundantly +in many parts of our country, produce so few berries? (<a href="#p-278">278</a>, <a href="#p-280">280</a>.)</p> + +<p>16. If the trumpet vine grows in your neighborhood, examine a number +of corollas and account for the dead ants found in them. Account also +for the large hole (sometimes three quarters of an inch in diameter) often +found near the base of the tube. (<a href="#p-281">281</a>.)</p> + +<p>17. Do you see any connection between the greater freshness and beauty +of flowers early in the morning, and the activity of bees, birds, and butterflies +at that time?</p> + +<p>18. The flowers most frequented by humming birds are the trumpet +honeysuckle, cardinal flower, trumpet vine, horsemint (<i>Monarda</i>), wild +columbine, canna, fuchsia, etc.; what inference would you draw from +this as to their color preferences?</p> +</div> + +<p><span class="pagenum" id="Page_249">[Pg 249]</span></p> + + +<h4 id="CH_VII_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>1. The ecology of the flower is so suggestive a subject and so peculiarly +appropriate to outdoor work that it seems hardly necessary to point out the +many attractive fields of inquiry it opens to the student of nature. In this +way alone can experiments in insect pollination be carried on to the best +advantage. Try the effect of enveloping buds of various kinds in gauze so +as to exclude the visits of insects, and note the result as to the production +of fruit and seed. Envelop a cluster of milkweed blossoms in this way and +notice how much longer the flowers so protected continue in bloom than do +the others; why is this? Try the same experiment upon the blooms of +cotton and hibiscus, if you live where they grow, and see whether the characteristic +change in color occurs in flowers from which insects have been +excluded, and whether good seed pods are produced by them. Try the +effect upon fruit production of excluding insects from clusters of apple, +pear, and peach blossoms.</p> + +<p>2. Make a list of all the outdoor plants, both wild and cultivated, that +are found blooming in your neighborhood, keeping a record of the earliest +specimens of each as you find them. The best way is to keep a sort of +daily calendar, and at the end of each month give a summary of the species +found in bloom during that period. In this way a fairly complete annual +record of the flowering time of the different plants for that vicinity will be +obtained. The record should be kept up the whole year round. Don’t +stop in winter, but go straight on through the coldest as well as the hottest +season, and you will make some surprising discoveries, especially if the +record is continued year after year. Give the common name of each plant, +adding the botanical one if you know it. Any facts that you may know +or may discover in regard to particular plants, such as their medicinal or +other uses, their poisonous or edible properties, the insects that visit them, +and in the case of weeds, their origin and introduction, will greatly enhance +the interest and value of the record.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_250">[Pg 250]</span></p> + +<h2 class="nobreak" id="CH_VIII">CHAPTER VIII. FRUITS</h2> +</div> + + +<h3 id="CH_VIII_I">I. HORTICULTURAL AND BOTANICAL FRUITS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Green ears of corn or wheat, fresh pods of beans, young +fruits of apple, grape, tomato, melon, buckeye, chestnut, or pecan. A +young fruiting stem of squash, gourd, or tomato.</p> + +<p><span class="smcap">Appliances.</span>—Coloring fluid, glasses of water, a piece of cardboard, +tin-foil, vaseline.</p> + +<p id="exp-87"><span class="smcap">Experiment 87. Where do the food substances contained in +fruits come from?</span>—Apply your food tests to the pulp of a young apple, +squash, bean pod, chestnut, buckeye, or a “green” ear of corn or wheat, +and see what it contains. Test the stem and roots of a plant of the same +kind in the same way. Do you find the same foods in them? Where +is the food stored?</p> + +<p id="exp-88"><span class="smcap">Experiment 88. Through what parts of the stem and fruit do +water and nourishment travel to the seed?</span>—Cut a young squash +or cucumber from the vine, leaving stem enough to insert by its cut end +in a glass of eosin solution. Leave for two or three days, then make a +vertical section through the stem and fruit. What course has the liquid +followed? Can you trace some of it into each seed? Do you see now a +use for the seed stalk and the rhaphe?</p> + +<p id="exp-89"><span class="smcap">Experiment 89. Does the surface of fruits give off water by +transpiration?</span>—Try <a href="#exp-59">Exp. 59</a>, using in place of leaves a young squash, +eggplant, or a bunch of grapes, and after a day or two notice whether +any moisture has been given off. If the fruit skin gives off moisture, +it is natural to expect that it would be provided with stomata, like other +transpiring organs. To find out whether this is so, place a thin piece of +the outer epidermis of a grape, tomato, plum, or apple under the microscope. +Do you find stomata on any of them? Do you see anything else? +Try the skin of an apple, and compare the corky dots you find there with +those on the bark of a young dicotyl stem <a href="#p-118">(118)</a> and decide what they are.</p> + +<p id="exp-90"><span class="smcap">Experiment 90. Will fruits ripen well in the absence of light +and air?</span>—Envelop a number of immature fruits in bags of dark cloth +or paper so that no light can reach them. Keep a number of others well +coated with oil or vaseline, and watch. Do the fruits so treated mature +as quickly or develop as fully as those of the same kind left untreated?</p> +</div> + +<p><span class="pagenum" id="Page_251">[Pg 251]</span></p> + + +<figure class="figcenter illowp45" id="i_261" style="max-width: 75em;"> + <img class="w100" src="images/i_261.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 12.</span>—The improvement of fruits by cultivation and selection: 1, the +common wild gooseberry; 2, Houghton gooseberry, seedling of the wild form; +3, Downing gooseberry, seedling of the Houghton. (All natural size, adapted from +Bailey.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_252">[Pg 252]</span></p> + +<div class="blockquot"> + +<p id="exp-91"><span class="smcap">Experiment 91. What is the use of the rind to the fruit?</span>—Select +two apples of equal size, peel one, and weigh both. After 12 to 24 +hours, weigh them again. Which shows the greater loss in weight? +Leave peeled and unpeeled fruits in an exposed place and see which is +the more readily attacked by insects. Which decays the sooner? What +are some of the uses of the rind?</p> +</div> + +<p id="p-282"><b>282. What is a fruit?</b>—Horticulturally and commercially +the distinction between a fruit and a vegetable depends very +much upon the use we make of it—whether as food, or as a +mere gratification of the palate. Broadly speaking, those +fruits that are lacking in sugar, as the tomato and cucumber, +are classed as vegetables. Botanically, a fruit is any +ripened seed vessel, or ovary, with such connected parts as +may have become incorporated with it; and hence, to the +botanist, a boll of cotton, a tickseed, or a cocklebur is just +as much a fruit as a peach or a watermelon.</p> + +<p id="p-283"><b>283. Classification of fruits.</b>—For convenience of description, +fruits are classed as:</p> + +<p>(<i>a</i>) Dry or fleshy, according as they have a more or less +hard and bony, or soft and fleshy, texture.</p> + +<p>(<i>b</i>) Dehiscent, or indehiscent, according as they open at +maturity in a regular way to discharge their seed, or remain +closed until the covering wears away or is burst by the germinating +embryo.</p> + +<p>Fleshy fruits are very seldom dehiscent, though some few, +as the balsam apple and the chayote, or one-seeded squash, +discharge their seed when mature. The banana and some +other fleshy fruits, when peeled, separate along regular lines, +and in this respect behave very much as if they were fleshy +pods.</p> + +<p id="p-284"><b>284. When is a fruit ripe?</b>—A fruit is ripe horticulturally, +when it is good to eat; it is ripe botanically, when it has set +its seed. Many of our choicest table fruits, such as the pineapple, +banana, and most varieties of fig, seldom are botanically +ripe, since they rarely produce perfect seeds.</p> + +<p>It is the constant effort of the horticulturist to develop<span class="pagenum" id="Page_253">[Pg 253]</span> +those parts of a plant that are useful to man, while in a state +of nature the plant seeks to develop such parts as best serve +its own purpose in the struggle for existence. The plants +most useful to man have, as a general thing, been subjected +to a long course of artificial breeding and selection. They +are forced developments, often monstrosities, from the plant’s +point of view, if we could conceive of it as capable of having +an opinion. Nature is continually striving to reclaim them; +and if left to themselves, they must +either obey “the call of the wild,” +or die out.</p> + +<figure class="figright illowp30" id="i_263" style="max-width: 30em;"> + <img class="w100" src="images/i_263.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 366.</span>—A seedless citrange, +hybrid between the orange +and the lemon.</p></figcaption> +</figure> + +<p id="p-285"><b>285. Seedless fruits and vegetables.</b>—As +the seed is the most +important thing to the plant, the +edible parts in wild fruits are, as a +rule, subsidiary to its development. +In a state of nature, fruits will generally +wither and drop from the +stem, if for any reason they have +become incapable of perfecting their +seed. It is only in a few kinds, limited to those which can +successfully propagate themselves by other means, that the +production of seed does not take place. Among cultivated +species, however, where propagation is carefully provided +for by man, the seed is of less importance, and sterile varieties +that might soon die out under natural conditions, continue +their existence indefinitely under his fostering hand. +The seeds of edible fruits are, as a general thing, both indigestible +and unpalatable <a href="#p-21">(21)</a>, and hence the efforts of the +horticulturist are directed largely to getting rid of them, or +to very greatly reducing their size and number in proportion +to the edible parts.</p> + +<p id="p-286"><b>286. How seedless fruits arise.</b>—The perfecting of seed +requires a great consumption of food and energy on the part +of the plant, and when it is led, for any reason, to expend +an unusual amount of force in some other function,—as<span class="pagenum" id="Page_254">[Pg 254]</span> +for instance, in producing tubers or in growing bulbs,—it +is apt to bear few seeds and to depend more or less completely +upon other methods of reproduction.</p> + +<p>Among cultivated plants, selection on the part of man, +whether conscious or unconscious, has perhaps contributed +more than any other cause to bring about the same result. +To this agency is probably due the development of our common +domestic fig, of which over four hundred varieties that +mature fruits without fertilization are cultivated in the United +States alone. The fig was one of the earliest fruits known to +cultivation; and the early navigators, ignorant of the processes +of fertilization, would naturally, in choosing specimens to +carry home with them, select only fruit-bearing trees. Such +of these as matured fruits would be preserved and propagated, +until, by repeated selection, hundreds of edible varieties have +been developed that ripen fruits without caprification <a href="#p-279">(279)</a>.</p> + +<p id="p-287"><b>287. The use of the fruit to the plant.</b>—The object of +the fruit is to furnish protection to the seeds during their +period of development and inactivity, and to aid in various +ways the work of dispersal. It probably takes part also in +digesting and diffusing nourishment for the use of the developing +seeds. It has been shown in previous chapters that plants, +almost without exception, are in the habit of storing up +food in various ways as a provision for fruiting. That a +large portion of the stored nourishment is used up in the performance +of this function is proved by its disappearance from +those parts—for example, from fleshy roots, such as beets +and turnips, after they have “gone to seed.”</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. What is the use of the down on the peach? The bloom of the plum +and grape? [<a href="#p-202">202</a>, (1); <a href="#exp-91">Exp. 91</a>.]</p> + +<p>2. Why are apples, pears, plums, and other fleshy fruits nearly always +rosier on one side than on the other? (<a href="#exp-90">Exp. 90</a>.)</p> + +<p>3. Can annuals be improved in any other way than by seed selection?</p> + +<p>4. Would a seedless annual be perpetuated under natural conditions?</p> + +<p><span class="pagenum" id="Page_255">[Pg 255]</span></p> + +<p>5. Why is decrease of moisture and increase of light desirable as the +fruiting season approaches? (<a href="#p-126">126</a>, <a href="#p-127">127</a>; <a href="#exp-90">Exp. 90</a>.)</p> + +<p>6. Why are turnips, carrots, and other fleshy roots unfit to eat if left +over till the plants have seeded? (<a href="#p-92">92</a>, <a href="#p-287">287</a>.)</p> +</div> + + +<h3 id="CH_VIII_II">II. FLESHY FRUITS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A specimen of each of the four principal kinds of fleshy +fruits. Examples of the pome are: apple, pear, quince, rose hip, haw; of +the berry: grape, tomato, cranberry, currant, gooseberry, lemon; of the +pepo: melon, squash, pumpkin; of the drupe: peach, plum, cherry, dogwood. +Specimens of the commoner kinds can nearly always be found in +the market; if nothing better is available, pickled and dried ones may be +used—figs, prunes, dates, raisins, etc.</p> +</div> + +<figure class="figright illowp40" id="i_265" style="max-width: 50em;"> + <img class="w100" src="images/i_265.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 367.</span>—Outside of an apple, showing +lenticels on the skin.</p></figcaption> +</figure> + + +<p id="p-288"><b>288. Dissection of a pome fruit.</b>—Examine with a lens +the outside of an apple or a pear. Can you make out the +lenticels? What difference +in color do you notice between +the ripe and unripe +fruit? What difference in +taste? What substance +would you judge from this, +do ripe fruits contain +which green ones do not? +Test both kinds for sugar +and starch; which contains +the more of each? Strictly +speaking, sugar and starch +are merely different forms +of the same chemical compound. In ripe fruits the starch +has been cooked by the sun and converted into sugar.</p> + +<p>With the point of a pencil separate the little dry scales that +cover the depression in the center of the fruit at the end opposite +the stem. How many of them are there? How does this +accord with the plan of the flower as outlined in <a href="#p-229">229</a>? They +are the remains of the sepals, as will be more apparent on +comparing them with the larger and more leaflike ones on +a hip, which is clearly only the end of the footstalk enlarged<span class="pagenum" id="Page_256">[Pg 256]</span> +and hollowed out with the calyx sepals at the top. Cut a +cross section midway between the stem and the blossom end, +and make an enlarged sketch of it. Label the thin, papery +walls that inclose the seed, <em>carpels</em>. +How many of them are there, and how +many seeds does each contain? The +carpels, together with all that portion +of the fruit which surrounds and adheres +to the ovary, constitute the <em>pericarp</em>, +or wall of the seed vessel. The +fleshy part of the apple is no part of +the ovary proper, but consists merely +of the receptacle, or end of the footstalk, +which becomes greatly enlarged +and thickened in fruit. Look for a +ring of dots outside the carpels, connected (usually) by a +faint scalloped line. How many of these dots are there? How +do they compare in number with the carpels? With the remnants +of the sepals adhering to the blossom end of the fruit?</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp70" id="i_266" style="max-width: 30em;"> + <img class="w100" src="images/i_266.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 368.</span>—Cross section +of a pome: <i>pl</i>, placenta; <i>c</i>, +carpels; <i>f</i>, fibrovascular bundles.</p></figcaption></figure> +</td><td> +<figure class="figcenter illowp60" id="i_266a" style="max-width: 50em;"> + <img class="w100" src="images/i_266a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 369.</span>—Vertical section +of a pome: <i>p</i>, peduncle; <i>f</i>, +fibrovascular bundles; <i>s</i>, seeds; +<i>pl</i>, placenta; <i>c</i>, carpel.</p></figcaption> +</figure></td></tr></table> + +<p>Next make a vertical section +through a fruit, and sketch, enlarging +it sufficiently to show all the +parts distinctly. Observe the line of +woody fibers outside the carpels, inclosing +the core of the apple. Compare +this with your cross section; to +what does it correspond? Where do +these threads originate? Where do +they end? Can you make out what +they are? (<a href="#p-176">176</a>.) Notice how and +where the stem is attached to the +fruit. Label the external portion of +the stem, <em>peduncle</em>; the upper part, from which the fibrovascular +bundles branch, the <em>receptacle</em>. It is the enlargement +of this which forms the fleshy part of the fruit. Try to find +out, with the aid of your lens and dissecting pins, the exact<span class="pagenum" id="Page_257">[Pg 257]</span> +spot at which the seeds are attached to the carpels, and +label this point, <em>placenta</em>. Notice whether it is in the axis +where the carpels all meet at their inner edges, or on the +outer side. Observe, also, whether the seed is attached to +the placenta by its big or its little end. If you can find a +tiny thread that attaches the seed to the carpel; label it, seed +stalk. Fruits of this kind are classed, botanically, as <em>pomes</em>. +Write, from your analysis, a definition of the pome.</p> + +<figure class="figright illowp35" id="i_267" style="max-width: 40em;"> + <img class="w100" src="images/i_267.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 370, 371.</span>—Enlarged +receptacle of Carolina allspice +(<i>Calycanthus</i>), containing fruits +attached to its inner surface: +370, exterior; 371, vertical section.</p></figcaption> +</figure> + +<p id="p-289"><b>289. Modifications of the receptacle.</b>—Compare with the +drawings you have made, a haw and a hip. What points of +agreement do you see? What differences? +Which of the two more +closely resembles the typical pome? +The receptacle is subject to a variety +of modifications, and forms a +part of many fruits, for example, +the fig, lotus, and calycanthus +(<a href="#i_267">Figs. 370, 371</a>); but a fruit is not +a pome unless the containing receptacle +becomes more or less soft +and edible.</p> + +<p id="p-290"><b>290. The pepo, or melon.</b>—Next +examine a gourd, cucumber, squash, +or any kind of melon, and compare its blossom end with that +of the apple or pear. Do you find any remains of a calyx, +or other part of the flower? Examine the peduncle and observe +how the fruit is attached to it. Can you tell what +made the outer epidermis of the rind? Put a small piece +under the microscope; do you see any stomata, or lenticels? +Cut cross and vertical sections, and sketch them, labeling +each part. There may be some difficulty in making out the +carpels, for they are not separate and distinct as in the pome, +but confluent with the enlarged receptacle, which in these +fruits forms the outer portion of the rind, and also with each +other at their edges, so as to form one unbroken circle, as if +they had all grown together. And this is precisely what<span class="pagenum" id="Page_258">[Pg 258]</span> +has happened. The placentas are greatly enlarged and +modified, and it may be necessary to refer to the diagram, +<a href="#i_268">Fig. 372</a>, <i>c</i>, in order to make them out. How many locules, +or chambers, are there in your specimen? How many +placentas? Notice that these are central +and double, but extend to the pericarp before +dividing so that they appear to be parietal, +and twice their real number, which +is only three. Are the seeds vertical, as in +the apple, or horizontal? Look for the +little stalk, or thread, that attaches them +to the placenta.</p> + +<p><em>Pepo</em> is the name given by botanists to +this kind of fruit. Write in your notebook +a proper definition of it, from the specimens examined.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp60" id="i_268" style="max-width: 20em;"> + <img class="w100" src="images/i_268.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 372.</span>—Cross +section of gourd: <i>c</i>, one +of the carpels in diagram. +(<i>After</i> <span class="smcap">Gray</span>.)</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_268a" style="max-width: 40em;"> + <img class="w100" src="images/i_268a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 373, 374.</span>—A potato +berry: 373, exterior; 374, cross +section.</p></figcaption> +</figure></td></tr></table> + +<p id="p-291"><b>291. The berry.</b>—Examine a tomato, an eggplant, a +grape, cranberry, lemon, or orange, in both cross and vertical +section, and compare it with the melon and the apple. +What differences and resemblances do you find? Cut a +cross section, and draw, showing the attachment of the seeds. +How many locules are there? Normally the tomato is a +two-celled fruit, like the potato berry (<a href="#i_268a">Fig. 374</a>), but it has +been so modified by cultivation that +the original plan is not always easy +to distinguish. See if you can make +it out. Do the seeds in your specimen +appear to be healthy and well +developed, or are some of them small +and aborted? How do you account +for this? (<a href="#p-285">285</a>, <a href="#p-286">286</a>.) What difference +do you notice in color between +the ripe and unripe fruit? Write a +definition of the berry from the study you have made of it.</p> + +<p>Berries are the commonest of all fleshy fruits, and the most +variable and difficult to define. In general, any soft, pulpy, +or juicy mass, like the grape and tomato, whether one or<span class="pagenum" id="Page_259">[Pg 259]</span> +many seeded, inclosed in a containing envelope, whether +skin or rind, is a berry. Its typical forms are such fruits as +the grape, mistletoe, pokeberry, etc., though such diverse +forms as the eggplant, persimmon, red pepper, orange, banana, +and pomegranate have been classed as berries; and, +in fact, the melon and the pumpkin are only greatly modified +kinds of the same fruit. In popular language, any small, +round, edible fruit is called a berry. This is a good commercial +classification, though not botanically correct.</p> + +<figure class="figright illowp25" id="i_269" style="max-width: 20em;"> + <img class="w100" src="images/i_269.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 375.</span>—Vertical +section of a +drupe. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-292"><b>292. The drupe, or stone fruit.</b>—Examine a section of a +green plum, peach, or cherry, before the stone has hardened, +and tell from what part it is formed. This stony covering, +composed of the inner layer of the pericarp, and enveloping +the seed like an outer coat, is the main distinction +between the drupe and the berry, +but it is not always possible to make out its +real nature except by an examination of the +young ovary. In a green drupe, before the +stone has hardened, its connection with the +fleshy part is very evident, and the ripe fruit +will answer inquiries if we know how to put +them. Open the stone, and the seed will be exposed with its +own coverings inside. When a stone has more than one +kernel,—for instance, an almond or peach stone, —the +stone is not a seed coat, but the hardened inner wall of a +seed vessel or ovary; for a seed coat can never contain more +than one seed, any more than the same skin can contain +more than one animal.</p> + +<p>All the fruits considered in this section belong to the fleshy +class. These form the bulk of the fruits sold in the market, +and are of special importance to the horticulturist.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Is the tomato horticulturally a fruit or a vegetable? the squash? +eggplant? cranberry? olive? elderberry? pepper? date? maypop? crab +apple? black haw? To what class does each belong? (<a href="#p-283">283</a>, <a href="#p-288">288-292</a>.)</p> + +<p><span class="pagenum" id="Page_260">[Pg 260]</span></p> + +<p>2. Of what use to the plant is the hard stone of the drupe? (21.)</p> + +<p>3. Is the pulp of fleshy fruits agreeable to the taste before they are +ripe? After? What advantage is this to the plant? (21.)</p> + +<p>4. Are the seeds of edible fruits, as a general thing, digestible or agreeable +to the palate?</p> + +<p>5. Is this an advantage to man? To the plant? (<a href="#p-21">21</a>, <a href="#p-284">284</a>, <a href="#p-285">285</a>.)</p> + +<p>6. What are the most common fleshy fruits in autumn?</p> + +<p>7. With what vegetative parts of the plant does the skin of many +fruits present correspondences? Are these such as to indicate homology, +or analogy only, between them? (<a href="#p-100">100</a>, <a href="#p-118">118</a>, <a href="#p-288">288</a>, <a href="#p-289">289</a>; <a href="#exp-89">Exp. 89</a>.)</p> + +<p>8. Name six of the most watery fruits that grow in your neighborhood.</p> + +<p>9. Under what conditions as to soil, heat, moisture, etc., does each +thrive best?</p> + +<p>10. Would a gardener act wisely to infer that because a fruit contains +a great deal of water it should be planted in a very wet place?</p> + +<p>11. Which contains more water, the fruit or the leaves of the apple?</p> + +<p>12. Why does not the fruit, when separated from the tree, wither as +quickly as do the leaves? (<a href="#exp-91">Exp. 91</a>.)</p> +</div> + + +<h3 id="CH_VIII_III">III. DRY FRUITS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Some easily attainable specimens of dry fruits are (1) nuts: +acorn, hickory nut, walnut, chestnut, pecan, filbert; (2) pods: pea and bean +pods, capsules of larkspur, milkweed, jimson weed, cotton; (3) grains: corn, +wheat, oats, rice; (4) akene: sunflower, thistle, dandelion, buckwheat, +clematis.</p> +</div> + +<p id="p-293"><b>293. Importance of dry fruits.</b>—Dry fruits are not in +general so conspicuous or so attractive as fleshy ones, but on +account of their great number and variety they offer a +wide field for study. They are also of great interest from an +economic point of view: (1) because they include the cereal +grains that furnish so large a portion of our food, and (2) +because the greater part of the troublesome weeds that infest +our crops are scattered by fruits of this class.</p> + +<p id="p-294" class='cb'><b>294. Indehiscent fruits.</b>—These kinds are so simple that +it will not be necessary to give much time to them. Compare +an acorn, a chestnut, or a filbert with a ripe bean pod or with +a capsule of morning-glory. Try to open each with your +fingers; which <em>dehisces</em>, or opens, the more readily? Which is +indehiscent, having no regular way of opening? How many<span class="pagenum" id="Page_261">[Pg 261]</span> +seeds or kernels do you find in the dehiscent pod? How +many in the indehiscent one? Would it be of any advantage +for a one-seeded pod to open? Remove the kernel +from the indehiscent fruit; has it any covering besides the +shell? Which is the pericarp, and which the seed coat?</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp80" id="i_271" style="max-width: 50em;"> + <img class="w100" src="images/i_271.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 376, 377.</span>—Nut of the pecan +tree: 376, exterior; 377, cross section.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_271a" style="max-width: 50em;"> + <img class="w100" src="images/i_271a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 378, 379.</span>—Nutlike seeds: +378, horse-chestnut; 379, seed of the +fetid sterculia.</p></figcaption> +</figure></td></tr></table> + +<p id="p-295"><b>295. The nut</b> is easily recognized by its hard, bony covering, +containing usually, when mature, a single large seed that +fills the interior. Care should be taken not to confound with +true nuts, large bony seeds, like those of the buckeye, horse-chestnut, +date, and the Brazil nut sold in the markets. In +the true nut, the hard covering is the seed vessel, or pericarp, +and not a part of the seed itself, though it often adheres to it +so closely as to seem so. In bony seeds, like those of the horse-chestnut +and persimmon, the hard covering is the outer seed +coat. The distinction is not always easy to make out unless +the seed can be examined while still attached to the placenta +of the fruit.</p> + +<table class='autotable'> +<tr><td class='wd40'> +<figure class="figcenter illowp80" id="i_271b" style="max-width: 30em;"> + <img class="w100" src="images/i_271b.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 380, 381.</span>—Akenes +(magnified): 380, of buckwheat; +381, of cinque-foil.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_272" style="max-width: 40em;"> + <img class="w100" src="images/i_272.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 382-384.</span>—Cremocarps, fruits of +the parsley family.</p></figcaption> +</figure></td></tr></table> + +<p id="p-296"><b>296. The akene</b>, of which we have +examples in the tailed fruit of the +clematis, the tiny pits on the strawberry, +and the so-called seeds of the +thistle, dandelion, and sunflower, is a +small, dry, one-seeded, indehiscent +fruit, so like a naked seed that it is +generally taken for one by persons not +acquainted with botany. It is the<span class="pagenum" id="Page_262">[Pg 262]</span> +commonest of all fruits, and there are so many kinds that +special names have been applied to some of the most marked +varieties. The akene of the +composite family may generally +be known by the +various appendages in the +form of scales, hooks, hairs, +or chaff, that crown it (<a href="#i_222">Figs. +309-314</a>). The fruits of the +parsley family are merely a +sort of double akene attached +by the inner face +to a slender stalk from which it separates at maturity.</p> + +<p>The <em>samara</em>, or key fruit, is an akene provided with a +wing to aid in its dispersion +by the wind. The +maple, ash, and elm furnish +familiar examples.</p> + +<table class='autotable'> +<tr><td class='wd70'> +<figure class="figcenter illowp80" id="i_272a" style="max-width: 40em;"> + <img class="w100" src="images/i_272a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 385, 386.</span>—Samaras: 385, ailanthus; +386, maple.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_272b" style="max-width: 20em;"> + <img class="w100" src="images/i_272b.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 387, 388.</span>—Grain +of wheat with husks on: +387, front view; 388, back +view.</p></figcaption> +</figure></td></tr></table> + +<p id="p-297"><b>297. The grain</b>, so familiar +to us in all kinds of +grasses, is economically +the most important of all +fruits. It is popularly +classed as a seed, and for practical purposes may be treated +as such, but it is really a modification of the akene in which +the seed coats have so completely fused with the pericarp +that they can no longer be distinguished +as separate organs. Peel the husk from +a grain of corn that has been soaked for +twenty-four hours, and you will find the +contents exposed without any covering; +remove the shell of an acorn or a hickory +nut, and the seed will still be enveloped +by its own coats. Would it be of any +advantage for the seed of an indehiscent fruit, like a grain of +corn or oats, to have a separate special covering of its own?</p> + +<p><span class="pagenum" id="Page_263">[Pg 263]</span></p> + +<table class='autotable wd80'> +<tr><td> +<figure class="figcenter illowp50" id="i_273" style="max-width: 30em;"> + <img class="w100" src="images/i_273.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 389.</span>—Follicle +of milkweed.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp50" id="i_273a" style="max-width: 30em;"> + <img class="w100" src="images/i_273a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 390.</span>—Leaflike +follicle of Japan +varnish tree: <i>S</i>, +outer (dorsal) suture; +<i>S′</i>, inner (ventral) +suture.</p></figcaption> +</figure></td></tr></table> + +<p id="p-298"><b>298. Dehiscent fruits.</b>—<em>Pod</em>, or <em>capsule</em>, is the general +name applied to all dehiscent fruits. The simplest possible +kind of pod is the <em>follicle</em>, composed of a +single carpel, like those of +the larkspur, milkweed, and +marsh marigold, and may be +regarded as a modified leaf. +Examine one of these pods +and you will find that it +splits down one side, which +corresponds to the edges of +the leaf brought together +and turned inward to form +a placenta for the attachment +of the seed. This line +of union is called a “suture,” +from a Latin word +meaning a “seam.”</p> + +<p id="p-299"><b>299. The legume.</b>—Get a pod of any kind of bean or +pea, and observe that it differs +from the follicle in having two +sutures or lines of dehiscence. +One of these runs along the back +of the carpel and corresponds +to the midrib of the leaf; the +other, corresponding to the +united edges of the carpellary +leaf, always turns inward, +toward the axis of the flower, +and forms the placenta.</p> + +<table class='autotable'> +<tr><td class='wd60'> +<figure class="figcenter illowp60" id="i_273b" style="max-width: 40em;"> + <img class="w100" src="images/i_273b.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 391-393.</span>—Legumes: 391, +legume of bean: <i>v</i>, ventral suture; +<i>d</i>, dorsal suture; 392, constricted +legume of senna (<i>Cassia Nelsonia</i>); 393, +legume of a pea, with partially constricted +pod.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_274" style="max-width: 20em;"> + <img class="w100" src="images/i_274.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 394.</span>—Loment of +beggar-ticks.</p></figcaption> +</figure></td></tr></table> + +<p>The beggar-ticks, so unpleasantly +familiar to most of us, +are merely a kind of legume constricted +between the seeds and +breaking up into separate joints +at maturity. What kind of<span class="pagenum" id="Page_264">[Pg 264]</span> +indehiscent fruits do the joints become +when separated? (<a href="#p-296">296</a>.)</p> + +<figure class="figright illowp50" id="i_274a" style="max-width: 50em;"> + <img class="w100" src="images/i_274a.jpg" alt=""> + <figcaption> +<table class="autotable"> +<tr> +<td class="tdl wd50"><p><span class="smcap">Fig. 395.</span>—Cross section of one-celled syncarpous capsule of frostweed, with parietal placentæ. +(<i>After</i> <span class="smcap">Gray</span>.)</p></td> +<td class="tdl"><p><span class="smcap">Fig. 396.</span>—Follicles of larkspur borne on the same torus, but distinct.</p></td> +</tr> +</table> +</figcaption> +</figure> + +<p id="p-300"><b>300. Compound or syncarpous pods.</b>—The +carpellary leaves may +unite either by their open +edges, as if a whorl like that +represented in <a href="#i_160">Fig. 188</a> were +to grow together by the +margins (<a href="#i_274a">Fig. 395</a>); or each +may first roll itself into a +simple follicle like the larkspur +and columbine (<a href="#i_274a">Fig. 396</a>), and then a number of +these may unite by their ventral sutures into a single syncarpous +capsule, with as many locules as there are carpels +(<a href="#fig_398">Fig. 398</a>). The seed-bearing sutures being all brought together +in the center, the placenta becomes <em>central</em> and <em>axial</em>. +In the first case (<a href="#i_274a">Fig. 395</a>) the open carpels form a one-chambered +capsule, though the placentas sometimes project, +as in the cotton, so far as to produce the effect of true +partitions with a central axial placenta. In capsules with<span class="pagenum" id="Page_265">[Pg 265]</span> +only one compartment, the number of carpels can generally +be determined by the number of sutures or of placentas.</p> + +<table class='autotable wd90'> +<tr> +<td class='tdc vab pm0'> +<figure class="figcenter illowp30 pmtb0" id="fig_397" style="max-width: 9.1875em;"> + <img class="w100" src="images/fig_397.jpg" alt=""> +</figure> +</td> +<td class='tdc vab pm0'> +<figure class="figcenter illowp35 pmtb0" id="fig_398" style="max-width: 10.5625em;"> + <img class="w100" src="images/fig_398.jpg" alt=""> +</figure> +</td> +<td class='tdc vab pm0'> +<figure class="figcenter illowp31 pmtb0" id="fig_399" style="max-width: 9.5625em;"> + <img class="w100" src="images/fig_399.jpg" alt=""> +</figure> +</td> +</tr> +<tr> +<td class='tdl vat caption wd30'><p> +<span class="smcap">Fig. 397.</span>—Pods of Echeveria, contiguous, but distinct.</p></td> +<td class='tdl vat caption wd30'><p> +<span class="smcap">Fig. 398.</span>—Capsule of +Colchicum, with carpels +united into a syncarpous +pod.</p></td> +<td class='tdl vat caption wd30'><p> +<span class="smcap">Fig. 399.</span>—Capsule +of corn cockle, with +free central placenta.</p></td> +</tr> +</table> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. To what class of fruits does each of the following belong—rice; +beggar-ticks; poppy; peanut; jimson weed; chinquapin; caraway?</p> + +<p>2. Is the coconut, as usually sold in the market, a fruit or a +seed?</p> + +<p>Suggestion: carefully examine the “eyes,” from without and from +within; if you can get a specimen with the husk on, it will help to a +decision.</p> + +<p>3. Can you name any syncarpous, or compound capsule, that is single-seeded?</p> + +<p>4. Can you name any indehiscent fruit that has normally more than +one seed?</p> + +<p>5. Give a reason for the difference. (23.)</p> + +<p>6. Name the weeds of your neighborhood that are most troublesome +on account of their adhesive fruits.</p> + +<p>7. Do these fruits belong, as a rule, to the dehiscent or to the indehiscent +class?</p> + +<p>8. Give a reason for the difference, if any is noted. (23.)</p> +</div> + + +<h3 id="CH_VIII_IV">IV. ACCESSORY, AGGREGATE, AND MULTIPLE FRUITS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—For autumn and winter, examples of accessory fruits +are: pineapple, common apple, pear, rose hip; aggregate: magnolia, +tulip tree, wild cucumber, sweet flag (<i>Calamus</i>); multiple: osage orange, +sweet gum balls, pine cones, figs, fresh or dried.</p> + +<p>For spring and summer, examples of accessory fruits are: raspberry, +strawberry, squash, cucumber; aggregate: strawberry, blackberry, Jack-in-the-pulpit; +multiple: fig, mulberry. Most of those named will be +found to belong to more than one class; the strawberry, for instance, is +both accessory and aggregate; the fig and pineapple, accessory and +multiple.</p> +</div> + +<p id="p-301"><b>301.</b> Besides the varieties already named, all fruits, +whether fleshy or dry, may be simple, accessory, aggregate, +or collective. Fruits of the first kind need no explanation; +they consist merely of a single ripened ovary,<span class="pagenum" id="Page_266">[Pg 266]</span> +whether of one or more carpels, as the peach, cherry, bean, +and lemon.</p> + +<figure class="figcenter illowp90" id="i_276" style="max-width: 50em;"> + <img class="w100" src="images/i_276.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 400, 401.</span>—Vertical sections showing the relation between a strawberry +flower and fruit: 400, the flower; 401, the fruit developed from it. The corresponding +parts are indicated by connecting lines; <i>r</i>, receptacle; <i>a</i>, sepal; <i>b</i>, petal; +<i>s</i>, stamens; <i>c</i>, carpel (akene in fruit); <i>p</i>, style of the pistil; <i>pl</i>, pulp of the fruit.</p></figcaption> +</figure> + +<p id="p-302"><b>302. Accessory fruits</b> are so called because some other +part than the seed vessel, or ovary proper, is coherent with, +or accessory to it, in forming the fruit, as in the apple and +the hip. The accessory part may consist of any organ, but +is more frequently the calyx or the receptacle. In the strawberry, +the little hard bodies, usually called seeds, that dot +the surface are the true fruits (akenes). A vertical section +through the center will show the edible part to consist +wholly of the enlarged receptacle. In the pineapple, the +edible stalk may be traced through a mass of flowers +whose seed vessels have become enlarged and ripened into +fruits.</p> + +<p id="p-303"><b>303. Aggregate fruits.</b>—Some accessory fruits, the strawberry +and blackberry for example, are, at the same time, +aggregate; that is, they are composed of a number of separate +individual fruits produced from a single flower. The +cone of the magnolia and of the tulip tree are aggregate +fruits; can you name any others?</p> + +<p><span class="pagenum" id="Page_267">[Pg 267]</span></p> + +<figure class="figright illowp60" id="i_277" style="max-width: 50em;"> + <img class="w100" src="images/i_277.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 402-404.</span>—Multiple fruit of the pineapple: +402, external view of a ripe fruit, showing the prolonged +receptacle growing into a new plant above, and the scaly +bracted covering below; 403, vertical section through the +axis of a fruit, showing <i>a</i>, the receptacle, with <i>b</i>, <i>b</i>, the +fleshy ovaries cohering around it and forming the edible +part of fruit; 404, a single “eye” or scale, somewhat +reduced, showing the scaly bract from the axil of which +the (generally) abortive flower originates.</p></figcaption> +</figure> + +<p id="p-304"><b>304. Collective, or multiple, fruits.</b>—The pineapple is an +example of both an accessory and a multiple fruit, being +composed of the +ripened ovaries of +a number of separate +flowers that +have become +more or less coherent. +The osage +orange, sweet +gum balls, fig, and +mulberry are +other examples +of this class.</p> + +<p id="p-305"><b>305. Dissection +of a multiple fruit.</b>—Get +one of the +dried figs sold by +the grocers. Look +at the small end +where the skin +originates; of what +part is it a modification? +(<a href="#p-289">289</a>.) +Can think of +a reason for this +curious, urnlike enlargement of the receptacle? Is there anything +about the fig, for instance, that renders it peculiarly +liable to be preyed upon by birds and insects? Could any +but a very small insect get through the eye without injuring +the fruit? Could it free itself from the sticky mass +inside and get out again without difficulty? Would you +judge from this that the caprification of the fig is easily +effected <a href="#p-279">(279)</a>, even when the fig wasp is present? Can you +now account for the fact that over four hundred varieties of +cultivated figs ripen their fruit without fertilization?</p> + +<p><span class="pagenum" id="Page_268">[Pg 268]</span></p> + +<figure class="figleft illowp25" id="i_278" style="max-width: 30em;"> + <img class="w100" src="images/i_278.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 405.</span>—Vertical section +of a fig, showing the +minute flowers inside the +closed receptacle.</p></figcaption> +</figure> + +<p>Open your specimen and examine the contents; what do +you find? From a dried specimen it will hardly be practicable +to make out clearly that the pulp of the fig consists of hundreds +of tiny pistillate blossoms that line the inner face of the +receptacle. The little grains usually +taken for seeds are really small akenes—the +ripened ovaries of flowers that +have been pollinated from the caprifig +(<a href="#p-279">279</a>, <a href="#p-286">286</a>). Crush one gently and examine +with a lens, or under a low power of +the microscope. It is these “botanically” +ripe fruits <a href="#p-284">(284)</a> that give to the dried +figs of commerce their plumpness and +their pleasant, nutty flavor. Why are +our native American figs lacking in these qualities <a href="#p-279">(279)</a>? +Could this defect be remedied? Do you know of any +efforts being made in that direction by American cultivators?</p> + +<figure class="figcenter illowp90" id="i_278a" style="max-width: 50em;"> + <img class="w100" src="images/i_278a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 406-409.</span>—Non caprificated and caprificated figs: 406, outside appearance +of non caprificated fig; 407, outside appearance of caprificated fig; 408, interior of +caprificated fig; 409, interior of non caprificated fig.</p></figcaption> +</figure> + +<p id="p-306"><b>306. Fruit clusters.</b>—Be careful not to confound aggregate +and collective fruits with mere clusters, like a bunch +of grapes or of sumac berries. The distinction is not always +easy to make out. The clump of akenes that make up a dandelion +ball, for instance, though held on a common receptacle, +like the mulberry and other collective fruits, have +so little connection with each other, and separate so completely +at maturity, as to partake more of the nature of a<span class="pagenum" id="Page_269">[Pg 269]</span> +cluster than of a collective fruit. The same is true of the +clump of tailed akenes that make up the fruit of the clematis. +Though the product of a single flower and thus technically +an aggregate fruit, they are really only a compact head or +cluster. Some degree of cohesion is necessary to constitute +a cluster of matured ovaries into an aggregate or a multiple +fruit.</p> + +<p id="p-307"><b>307. The individual fruits</b> that make up the various kinds +just described may belong to any of the classes mentioned +in the two preceding sections: those of the blackberry, for +instance, are drupes; of the strawberry, akenes; of the +sweet gum, capsules.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. To what class of fruits would you refer the following: a banana; +a tickseed; a dewberry; a cocklebur; a string bean; a watermelon; a +cantaloupe; a pomegranate; a black haw; a dogwood berry; a red +pepper?</p> + +<p>2. Tell which of the following are aggregate or multiple fruits, and +which are fruit clusters: an ear of corn; of wheat; a buttonwood or a +sycamore ball; a hop; a dewberry; a pine cone; a prickly pear. (<a href="#p-303">303</a>, +<a href="#p-304">304</a>, <a href="#p-306">306</a>.)</p> + +<p>3. Tell the nature of the individual fruits composing the different combinations +mentioned in the last question.</p> + +<p>4. Can you suggest any advantage that might accrue to a species from +having its fruits clustered or compound? (<a href="#p-21">21</a>, <a href="#p-23">23</a>, <a href="#p-24">24</a>, <a href="#p-287">287</a>.)</p> +</div> + + +<h4 id="CH_VIII_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>1. Study the various edible fruits of your neighborhood with regard to +their means of dissemination and protection. Consider the object of the +protective adaptations in each case, whether against heat, cold, moisture, +animals, etc. Notice the color of the different kinds, and trace its significance; +for example, the bright red of the holly, the dull color of muscadine, +black haw, and wild smilax. Account for the prevalence of red +among autumn fruits. Notice the position of the fruit on the bough and +explain its object; as, for instance, the clustering of dogwood at the end +of the twig, the pendent position of grapes and honey locusts. Observe<span class="pagenum" id="Page_270">[Pg 270]</span> +the relation between the color and size of fruits and their grouping. What +advantage is it for sumac and bird haws to be gathered in large clusters?</p> + +<p>2. Compare wild with cultivated fruits and notice in what respects man +has altered the latter for his own benefit. Note, for instance, the difference +between cultivated apples and the wild crab, between the cultivated +grains and wild grasses. Observe the great number of varieties of each +kind in cultivation and try to account for it.</p> + +<p>3. Notice the situations in which different kinds of fruits grow, whether +hot, dry, moist, windy, or sheltered, and how they are affected by their +surroundings. For example, account for the difference between blackberries +growing on a dry hillside, and those in moist land along the borders +of a stream. Give the conclusions drawn from your observations in each +case.</p> + +<p>4. Notice what animals feed upon the different kinds, and whether their +visits are harmful or beneficial. Consider in what respects the interests +of the plant itself, the interests of man, and the interests of other animals +may clash or coincide. Examine the vegetation along the hedgerows and +borders of fields and old fences. Notice the kind of plants that compose +it—sumac, sassafras, cedars, cat brier, etc. The list will be slightly +different for different localities, but this will not alter the general conclusion. +What kinds of fruits and seeds do these shrubs produce? What +kinds of living creatures frequent hedgerows and feed upon the seeds of +such plants? Do you see any relation between these facts and one of the +modes of seed dispersal?</p> + +<p>5. Classify all the fruits you have collected during your walk, under their +proper heads, as fleshy or dry, dehiscent or indehiscent, simple, accessory, +aggregate, collective. Be careful to distinguish between compact clusters, +like the heads of clematis or buttonwood, and truly compound fruits.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_271">[Pg 271]</span></p> + +<h2 class="nobreak" id="CH_IX">CHAPTER IX. THE RESPONSE OF THE PLANT +TO ITS SURROUNDINGS</h2> +</div> + + +<h3 id="CH_IX_I">I. ECOLOGICAL FACTORS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A number of small flowerpots filled with soils of as many +different kinds as can be found in the neighborhood.</p> +</div> + +<p id="p-308"><b>308. Definition.</b>—By <em>ecology</em> is meant the relation of +plants to their surroundings, which may be considered under +three general heads: their relations to inanimate nature, +to other plants, and to animals. The subject has been +touched upon repeatedly in the foregoing pages, and, in +fact, it is impossible to treat of any branch of botany without +some reference to it. All that was said about the adjustment +of leaves for light and moisture, and their adaptations +for protection and food storage, about the devices +for pollination, and for fruit and seed dispersal, really +belong to ecology.</p> + +<p id="p-309"><b>309. Symbiosis.</b>—The relations of plants to animate +nature are <em>biological factors</em>, and may act in two ways: +(1) through the destruction of vegetation by hungry animals +and by parasitic and disease-producing organisms; +and (2) by associations for mutual benefit, such as are +described in section viii of chapter VII. Associations of +this kind are included under the general term <em>symbiosis</em>, +a word which means “living together.” In its broadest +sense symbiosis refers to any sort of dependence or intimate +organic relation between different kinds of individuals, and +so may include the climbing and parasitic habits; but it +is usually restricted to cases where the relation is one of +mutual benefit. It may exist either between plants of one +kind with those of another, between animals with animals, +or between plants and animals, as in the case of the clover +and bumblebee, and the yucca and pronuba.</p> + +<p><span class="pagenum" id="Page_272">[Pg 272]</span></p> + +<figure class="figcenter illowp50" id="i_282" style="max-width: 75em;"> + <img class="w100" src="images/i_282.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 13.</span>—Showing the quick response of vegetation to surroundings. The +upper cut shows the appearance of an irrigation canal in the arid plains region, +when first completed; the lower cut, ten years after completion.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_273">[Pg 273]</span></p> + +<p>The occurrence of root tubercles on certain of the leguminosæ +<a href="#p-63">(63)</a> is a clear case of symbiosis, the microscopic +organisms in the tubercles getting their food from the plant +and at the same time enabling it to get food for itself from +the air in a way that it could not otherwise do.</p> + +<p id="p-310"><b>310. Relations with inanimate nature.</b>—But it is to the +relations of plants with inanimate nature, and their grouping +into societies under the influence of such conditions, +that the term “ecology” is more strictly applied. The +external conditions that lead to the grouping are called +<em>ecological factors</em>. The most important of these are temperature, +moisture, soil, light, and air, including the direction +and character of the prevailing winds. Each of these +factors is complicated with the others and with conditions +of its own in a way that often makes it difficult to determine +just what effect any one of them may have in the formation +of a given plant society.</p> + +<p id="p-311"><b>311. Temperature</b> may be even and steady, like that of +most oceanic regions, or it may be subject to sudden caprices +and variations, like the “heated terms” and “cold +snaps” that afflict our Eastern coast region every few years. +It is not the average temperature of a climate, but its +extremes, especially of cold, that limit the character of +vegetation.</p> + +<p>Temperature probably has more influence than any other +factor upon the distribution of plants over the globe; but it +can have little or no effect in evolving local differences in +vegetation, because the temperature of any given locality, +except on the sides of high mountains, will ordinarily be the +same within a circuit of many miles.</p> + +<p id="p-312"><b>312. Moisture</b>, again, may be of all degrees, from the +superabundance of lakes and rivers and standing swamps, +to the arid dryness of the desert, and the water may be<span class="pagenum" id="Page_274">[Pg 274]</span> +still and sluggish, or in rapid motion. It may exist more +or less permanently in the atmosphere, as in moist climates +like those of England and Ireland, where vegetation is +characterized by great verdure; or it may come irregularly +in the form of sudden floods, or at fixed intervals, causing +an alternation of wet and dry seasons. Moreover, the +moisture of the soil or the atmosphere may be impregnated +with minerals or gases, which may affect the vegetation +independently of the actual amount of water absorbed.</p> + +<figure class="figcenter illowp75" id="i_284" style="max-width: 50em;"> + <img class="w100" src="images/i_284.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 410.</span>—The effect of cold—a Mt. Katahdin bog. (<i>From</i> Mo. Botanical +Garden Rep’t.)</p></figcaption> +</figure> + +<p>Snow is a form of water which may act in two entirely +opposite ways: (1) by keeping the atmospheric precipitation +locked up in a solid state and thus bringing about a +condition analogous to drought—for example, in arctic deserts +and Alpine snow fields; (2) by causing annual floods +and overflows when it melts in the spring, as in the Nile +and Mississippi valleys.</p> + +<p>In cold temperate regions it also influences vegetation<span class="pagenum" id="Page_275">[Pg 275]</span> +to a considerable extent by covering the warm earth like +a blanket during winter, and thus protecting tender seeds +and shoots that otherwise would not be able to survive.</p> + +<figure class="figright illowp40" id="i_285" style="max-width: 40em;"> + <img class="w100" src="images/i_285.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 411.</span>—Dogwood, a tree tolerant +of shade, growing and blooming in a deeply +wooded glen.</p></figcaption> +</figure> + +<p id="p-313"><b>313. Light</b> may be of all +degrees of intensity, from the +blazing sun of the treeless +plain to the darkness of caves +and cellars where no green +thing can exist. Between +these extremes are numberless +intermediate stages: the +dark ravines on the northern +side of mountains, the dense +shade of beech and hemlock +forests, and the light, lacy +shadows of the pines,—each +characterized by its peculiar +form of vegetation. Absence +of light, too, is usually accompanied by a lowering of temperature +and a reduction of transpiration, factors which tend to +accentuate the difference between sun plants and shade +plants, giving to the latter some of the characteristics of +aquatic vegetation. Generally, the +tissues of these are thin and delicate, +and having no need to guard +against excessive transpiration, they +wither rapidly when cut or exposed +to too great intensity of heat and +light.</p> + +<table class='autotable wd90'> +<tr><td class='wd60'> +<figure class="figcenter illowp60" id="i_285a" style="max-width: 30em;"> + <img class="w100" src="images/i_285a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 412.</span>—A red cedar grown +in a barren, wind-beaten situation.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp60" id="i_286" style="max-width: 20em;"> + <img class="w100" src="images/i_286.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 413.</span>—A red +cedar grown under +normal conditions.</p></figcaption> +</figure></td></tr></table> + +<p id="p-314"><b>314. Winds</b> affect vegetation, not +only as to the manner of seed distribution +and the conveyance of pollen, +but directly by increasing transpiration, and necessitating +the development of strong holdfasts in plants growing +upon mountain sides and in other exposed situations. The +nature of the region from which they blow—whether moist,<span class="pagenum" id="Page_276">[Pg 276]</span> +dry, hot, cold, etc.—is also an important +factor. In a district open to sea breezes, +live oaks, which require a salt atmosphere, +may sometimes be found as far as a hundred +miles from the coast.</p> + +<p id="p-315"><b>315. Soil.</b>—While water is the most important, +soil is perhaps the most interesting +of these factors to the farmer, because it is +the one that he has it most largely in his +power to modify. It is to be viewed under +two aspects: first, as to its mechanical properties, +whether soft, hard, compact, porous, +light, heavy, etc.; secondly, as to its chemical +composition and the amount of plant food-materials +contained in it. The first can be +regulated by tillage and drainage, the second by a proper +use of fertilizers.</p> + +<div class="blockquot"> + +<p id="exp-92"><span class="smcap">Experiment 92. To show the influence of soil as an ecological +factor.</span>—Fill a number of small earthen pots with all the different kinds +of soil that are to be found in your neighborhood. Keep well moistened +and make a list of the plants that appear spontaneously in each. Is +there any difference in the kinds produced by different soils? In vigor +or abundance of the same or different kinds? Do more seedlings appear +in any of the pots than could live if left alone? What becomes of a majority +of the seedlings that come up in a state of nature?</p> + +<p>After a time, stop watering until all the plants are dead and new ones +cease to appear. Notice the rate at which vegetation dies out in each +and the kind of plants that can live longest without water. Which of the +different soils is capable of sustaining vegetation longest without a fresh +supply of moisture? To what quality of the soil is this due? (<a href="#exp-53">Exp. 53</a>.)</p> +</div> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Is the relation between man and the plants cultivated by him a +symbiosis? (<a href="#p-309">309</a>.)</p> + +<p>2. Why is it that plants of the same, or closely related species are found +in such different localities as the shores of Lake Superior, the top of Mt. +Washington, and the Black Mountains in North Carolina? (<a href="#p-311">311</a>, <a href="#p-330">330</a>.)</p> + +<p><span class="pagenum" id="Page_277">[Pg 277]</span></p> + +<p>3. Which of the five ecological factors mentioned in paragraphs <a href="#p-311">311-315</a> +has probably most largely influenced their distribution?</p> + +<p>4. What is the prevailing character of the soil in your neighborhood?</p> + +<p>5. Is your climate moist or dry? Warm or cold?</p> + +<p>6. Can you trace any connection between these factors and the prevailing +types of vegetation?</p> +</div> + + +<h3 id="CH_IX_II">II. PLANT ASSOCIATIONS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—The subject is not well suited to laboratory work, though, +if time permits, it is recommended that a detailed study be made of at +least one typical hydrophyte, halophyte, and xerophyte plant. Some +good examples are: (1) Hydrophyte: pond weed, waterlily, pipewort (<i>Eriocaulon</i>), +bladderwort, arrowhead (<i>Sagittaria</i>); (2) Halophyte: sea lavender, +sea rocket, sea lettuce, water hyacinth; (3) Xerophyte: cactus, century +plant, pineapple, stonecrop, purslane, lichen.</p> +</div> + +<p id="p-316"><b>316. Modes of grouping.</b>—Plants group themselves in +their favorite habitats, not according to their botanical relationships, +but with regard to the predominance of one or +more of the ecological factors that influence their growth. +Sometimes one or two species will take practical possession +of large areas, like the coarse grasses that spread over certain +salt marshes, or the pines that formerly constituted the sole +forest growth over extensive regions in North Carolina and +Maine. Exclusive growths of this kind over limited areas +are sometimes called plant <em>colonies</em>, and the individuals composing +them belong, as a general thing, to the hardy, pushing +sort known as “pioneers,” which are among the first to take +possession of new soil and force their way into unoccupied +territory. But more usually we find a great diversity of +forms brought together by their common requirements as +to shade, soil, moisture, and other external conditions.</p> + +<p>Any well-defined assemblage of plants, whether of one kind +or many, originating in such a common response to the same +influences, is called a <em>formation</em>. These associations are variously +classed, according to the nature of their habitat, +as salt water, fresh water, sand hill, swamp, bog, river bottom, +or such other kinds as their ecological character may<span class="pagenum" id="Page_278">[Pg 278]</span> +indicate. Local conditions in limited areas may lead to the +segregation of smaller and more compact groups called <em>societies</em>. +This term, however, is used rather loosely, being treated +in some works as synonymous with formations, in others as +analogous with what have here been defined as colonies.</p> + +<figure class="figcenter illowp75" id="i_288" style="max-width: 50em;"> + <img class="w100" src="images/i_288.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 414.</span>—A colony of Alabama primroses (<i>Œnothera speciosa</i>).</p></figcaption> +</figure> + +<p id="p-317"><b>317. Principles of subdivision.</b>—The mixed associations +described in the last paragraph are quite independent of +botanical relationships, and any of the factors named in +<a href="#p-310">310</a>, or others of a different kind, could be made the basis of +their classification. They might be grouped, for instance, +according to their economic uses, or according to origin, +whether native or introduced, as best suited the purpose of +the classification in each case. The moisture factor, however, +has been generally agreed upon as the one most convenient +for ordinary purposes. Upon this principle plants are divided +into three great groups:—</p> + +<p><span class="pagenum" id="Page_279">[Pg 279]</span></p> + +<p><b>Hydrophytes</b>, or water plants, those that require abundant +moisture.</p> + +<p><b>Xerophytes</b>, or drought plants, those that have adapted +themselves to desert or arid conditions.</p> + +<figure class="figright illowp25" id="i_289" style="max-width: 20em;"> + <img class="w100" src="images/i_289.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 415.</span>—A water +plant (<i>Limnophila</i>), +with water leaves and +air leaves and transitional +forms.</p></figcaption> +</figure> + +<p><b>Mesophytes</b>, plants that live in conditions intermediate +between excessive drought and excessive +moisture. To this class belong most of +our ordinary cultivated plants and the +greater part of the vegetation of the globe.</p> + +<p><b>Halophytes</b>, “salt plants,” is a term +used to designate a fourth class, based not +directly upon the water factor, but upon +the presence of a particular mineral in the +water or the soil which they can tolerate. +They seem to bear a sort of double relation +to hydrophytes on the one hand and +to zerophytes on the other.</p> + +<p id="p-318"><b>318. Hydrophyte societies.</b>—These embrace +a number of forms, from those inhabiting +swamps and wet moors, to the +submerged vegetation of lakes and rivers. +An examination of almost any kind of +water plant will show some of the physiological +effects of unlimited moisture. Take +a piece of pondweed, or other immersed +plant, out of the water and notice how completely +it collapses. This is because, being +buoyed up by the water, it has no need to +spend its energies in developing woody +tissue. Floating and swimming plants will +generally be found to have no root system +or very small ones, because they absorb +their nourishment through all parts of the +epidermis directly from the medium in which they live. +That they may absorb readily, the tissues are apt to be soft +and succulent and the walls of the cells composing them<span class="pagenum" id="Page_280">[Pg 280]</span> +very thin. In some of the pipeworts (<i>Eriocaulon</i>), the ells +are so large as to be easily seen with the unaided eye. If +you can obtain one of these, examine it +with a lens and notice how very thin the +walls are. Water plants also contain numerous +air cavities, and often develop +bladders and floats, as in the common bladderwort +and many +seaweeds. The leaves +of submerged plants +are usually either +greatly reduced in size +or very much cut and +divided, while the ones +that rise above water, +like those of the water +lily, are apt to be large +and entire, to facilitate floating, and have +stomata on their upper surface. Floating +plants sometimes form such large +colonies as to be a serious menace to +navigation. Well-known instances of +this are the water hyacinths in the St. +John’s River, Florida, and the vast +formations of swimming gulfweed from +which the Sargasso Sea takes its name.</p> + +<table class='autotable wd80'> +<tr><td> +<figure class="figcenter illowp50" id="i_290a" style="max-width: 20em;"> + <img class="w100" src="images/i_290.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 416.</span>—Seaweed +(<i>sargassum</i>) with bladderlike +floats.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp50" id="i_290" style="max-width: 20em;"> + <img class="w100" src="images/i_290a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 417.</span>—A pioneer +swamp colony of cattails. +(<i>From</i> a photograph by +Harry B. Shaw, U.S. Dept. +Agr.)</p></figcaption> +</figure></td></tr></table> + +<p id="p-319"><b>319. Swamp societies.</b>—These include +what may be regarded as the amphibious +portion of the hydrophyte +group. They compose the sedge and +cattail bogs, reed jungles, moss and fern +thickets, forests of cypress, magnolia, +black gum, pine, tamarack, balsam, and +the like. The sedges and cattails are the pioneers of these +societies, which tend constantly to encroach upon the water +and so prepare the way for the advance of other colonists.<span class="pagenum" id="Page_281">[Pg 281]</span> +Drawing their nourishment from the loose soil in which they +are anchored, and lacking the support of a liquid medium, +they develop roots and vascular stems. The roots of plants +growing in swamps have difficulty in obtaining proper aëration +on account of the water, which shuts off the air from +them; hence they are furnished with large air cavities, and +the bases of the stems are often greatly enlarged, as in the +Ogeechee lime (<i>Nyssa capitata</i>) and cypress, to give room +for the formation of air passages. The peculiar hollow projections +known as “cypress knees” are arrangements for +aërating the roots of these trees.</p> + +<figure class="figcenter illowp90" id="i_291" style="max-width: 50em;"> + <img class="w100" src="images/i_291.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 418.</span>—A Southern cypress swamp, showing on the left the peculiar enlargements +for aëration, known as “cypress knees.” (<i>From</i> Mo. Botanical Garden Rep’t.)</p></figcaption> +</figure> + +<p id="p-320"><b>320. Xerophyte societies</b> are <a id="tn_281">adapted</a> to conditions the +reverse of those affected by hydrophytes. The extreme of +these conditions is presented by regions of perennial drought, +like our Western arid plains and the great deserts of the interior +of Asia and Africa. Under these conditions plants +have two problems to solve,—to collect all the moisture they +can and to keep it as long as they can. Hence, plants of +such regions have a diminished evaporating surface, owing +to the absence of foliage and the compacting of their tissues +into the stem, after the manner of the cactus and prickly +euphorbia; or their leaves may become thick and fleshy so +as to resist evaporation and retain large amounts of moisture, +as in the case of the yucca and century plant. They +also frequently develop a thick, hard epidermis, or cover +themselves with protective hairs and scales.</p> + +<p>The principal types of xerophyte plants are: (1) the lichens, +mosses, and saxifrages found on bald rocks and mountain +cliffs; (2) sand plants, such as cockspur grass, sand spurry, +wiregrass, and the like, inhabiting sea beaches and pine +barrens; (3) the sage brush, greasewood, and switch plants +of our Western alkali plains; (4) the cactus and yuccas of +southern California, Arizona, and Mexico; (5) the acacias, +agaves, and hardy “chapparal” thickets of southern Texas +and Mexico. The first class are of importance as the pioneers +and pathfinders of the xerophyte community. In +tropical and polar deserts alike they are the first settlers, +and by aiding in the disintegration of rocks and their gradual +conversion into soil, they pave the way for the coming of +the higher plants, and it may be of man himself.</p> + +<p><span class="pagenum" id="Page_282">[Pg 282]</span></p> + +<figure class="figcenter illowp90" id="i_292" style="max-width: 50em;"> + <img class="w100" src="images/i_292.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 14.</span>—A xerophyte formation of yuccas, cacti, and switch plants, near Zacatecas, Mexico. +(<i>From</i> a photograph by Professor F. E. Lloyd.)</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_283">[Pg 283]</span></p> + +<p id="p-321"><b>321. Partial xerophytes.</b>—Plants exposed to periodic +and occasional droughts frequently provide against hard +times by laying up stores of nourishment in bulbs and rootstocks +and retiring underground until the stress is over. +This is known as the <em>geophilous</em>, or earth-loving, habit. +Others, as some of the lichens, and the little resurrection +fern (<i>Polypodium incanum</i>, <a href="#i_294">Figs. 419, 420</a>), so common on the +trunks of oaks and elms in the Southern States, make no +resistance, but wither away completely during dry weather, +only to waken again to vigorous life with the first shower.</p> + +<figure class="figcenter illowp50" id="i_294" style="max-width: 50em;"> + <img class="w100" src="images/i_294.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 419, 420.</span>—A resurrection fern: 419, in dry weather; 420, after a shower.</p></figcaption> +</figure> + +<p id="p-322"><b>322. Physiological xerophytes.</b>—Plants growing in thin +or poor soil, such as that on denuded hillsides, fresh railroad +cuts, and newly graded streets, are apt to take on a more or +less xerophytic character, even though there may be no lack +of moisture. Such soils are called “new” because the +mineral elements in them have not been exposed long enough<span class="pagenum" id="Page_284">[Pg 284]</span> +to have become decomposed and mixed with humus, and the +vegetation that first populates them has to do the pioneer +work of disintegrating and impregnating the substratum with<span class="pagenum" id="Page_285">[Pg 285]</span> +humus. For similar reasons the vegetation of sandy bogs +and sea beaches, owing to the poverty of the soil in nitrogenous +matter, usually develops xerophyte adaptations, +even though there may be a superabundance of moisture. +Plants growing on high mountain tops and in cold arctic +bogs take on the same characteristics (<a href="#i_284">Fig. 410</a>). Such situations +are said to be “physiologically dry,” because the +moisture they have is not in a condition to be readily absorbed. +The vegetation of arctic regions suffers more from +physiological drought than from cold.</p> + +<figure class="figcenter illowp90" id="i_295" style="max-width: 50em;"> + <img class="w100" src="images/i_295.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 421.</span>—A halophyte swamp of mangroves. Notice the tangle of adventitious +prop roots assisting in the work of absorption from the brackish marsh soil. +(<i>From</i> Mo. Botanical Garden Rep’t.)</p></figcaption> +</figure> + +<p id="p-323"><b>323. Halophytes</b> include plants growing by the seashore +and the vegetation around salt springs and lakes and that of +alkali deserts. Seaweeds are in a sense halophytes, since +they live in salt water, but as they are true aquatic plants +and exhibit many of the peculiarities of hydrophytes in their +mechanical structure, they are classed with them. The +name <em>halophyte</em> applies more particularly to land plants<span class="pagenum" id="Page_286">[Pg 286]</span> +that have adapted themselves to the presence in the soil +or in the atmospheric vapor, of certain minerals, popularly +known as salts, which cause them to take on many xerophyte +characteristics. The reason for this, as was shown in +Exp. 39, is because the mixture of salt in the water of the +soil increases its density so that it is difficult for the plant to +absorb as much as it needs, and thus halophytes are living +under “physiologically” xerophyte conditions. If you have +ever spent any time at the seashore, you cannot fail to have +observed the thick and fleshy habit exhibited by many of +the plants growing there, such as the samphire, sea purslane +(<i>Sesuvium</i>), and sea rocket (<i>Cakile</i>). A form of goldenrod +found by the seashore has thick, fleshy leaves, and is as hard +to dry as some of the fleshy xerophytes.</p> + +<p>Another characteristic of desert plants that is common +also to seaside vegetation is the frequent occurrence of a +thick, hard epidermis, as in the sea lavender and saw grass. +The live oaks, trees that love the salt air and never flourish +well beyond reach of the sea breezes, have small, thick, +hard leaves, very like those of the stunted oaks that grow on +the dry hills of California. The presence of spines and +hairs, it will be observed, is also very common; <i>e.g.</i> the salsola, +the sea oxeye, and the low primrose (<i>Œnothera humifusa</i>). +In other cases the leaf blades are so strongly involute +or revolute <a href="#p-202">(202)</a> as to make them appear cylindrical. All +these, it will be observed, are xerophyte adaptations, and the +object in both cases is the same—the conservation of moisture.</p> + +<p id="p-324"><b>324. Mesophytes.</b>—These embrace the great body of +plants growing under the ordinary conditions of temperate +regions, which may vary from the liberal water supply of +low meadows and shady forests to the almost desert barrenness +of dusty lanes and gullied, treeless hillsides. The +forms and conditions they present are so varied that it would +be impracticable to consider them all in a work like this, but +they may be summed up under the two general heads of<span class="pagenum" id="Page_287">[Pg 287]</span> +(1) <em>open ground</em> and (2) <em>woodland</em>. Under the first are included: +(<i>a</i>) all cultivated grounds—fields, meadows, lawns, +pastures, and roadsides, with their characteristic shrubs, +flowers, and grasses; (<i>b</i>) heaths and plains of northern or +alpine regions, with their low, stunted perennials and bright, +but fugacious, flowers. Under the second are classed all +woods, thickets, and copses, with the shrubs and herbs that +form their undergrowth. These may be grouped in three +main divisions: (<i>c</i>) mixed forests of maple, ash, oak, hickory, +birch, sweet gum, etc.; (<i>d</i>) pure forests of pine, balsam, fir, +cypress, and the like; and finally (<i>e</i>), the perennial splendors +of the tropical forest, where the vegetation of the globe +reaches its climax in luxuriance and variety of growth.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why do florists cultivate cactus plants in poor soil? (<a href="#p-320">320</a>.)</p> + +<p>2. What would be the effect on such a plant of copious watering and +fertilizing?</p> + +<p>3. Why must an asparagus bed be sprinkled occasionally with salt? +(<a href="#p-323">323</a>.)</p> + +<p>4. If a gardener wished to develop or increase a fleshy habit in a plant, +to what conditions of soil and moisture would he subject it? (<a href="#p-320">320</a>, <a href="#p-323">323</a>.)</p> + +<p>5. What difference do you notice between blackberries and dewberries +grown by the water and on a dry hillside?</p> + +<p>6. Are there corresponding differences in the root, stem, and leaves of +plants growing in the two situations, and if so account for them?</p> + +<p>7. When a tract of dry land is permanently overflowed by the building +of a dam or levee, why does all the original vegetation die, or take on a +sickly appearance? (<a href="#p-319">319</a>.)</p> + +<p>8. Should plants with densely hairy leaves be given much water, as +a general thing? (<a href="#p-202">202</a>, <a href="#p-320">320</a>.)</p> + +<p>9. A farmer planted a grove of pecan trees on a high, dry hilltop; +had he paid much attention to ecology? Give a reason for your answer.</p> + +<p>10. Why do the branches of trees often die, or fail to develop, on the +windward side? (<a href="#p-314">314</a>.)</p> + +<p>11. Why do trees grown in dry soil have harder wood than the same +kind grown in wet soil? (<a href="#p-123">123</a>, <a href="#p-318">318</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_288">[Pg 288]</span></p> + + +<h3 id="CH_IX_III">III. ZONES OF VEGETATION</h3> + +<figure class="figright illowp60 mth" id="i_298" style="max-width: 50em;"> + <img class="w100" src="images/i_298.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 422.</span>—A pioneer colony of sumac growing on +a railroad cutting. (<i>From</i> a photograph by J. M. +Coulter.)</p></figcaption> +</figure> + +<p id="p-325"><b>325. The origin of vegetable zones.</b>—The terms “zone” +and “zonation” are used to express a general tendency of +plant societies and formations to distribute themselves in +more or less regular belts or strata, relatively to the varying +intensity of the prevalent ecological factor of their habitat. +In almost every locality there exists some special feature—a +pond, a brook, a small ravine, an isolated hilltop, a deserted +quarry, a gravel pit, or a railroad cut,—sufficiently distinct +from the general surroundings to exercise a perceptible +control over the +vegetation in its +immediate vicinity, +and thus to become +the starting point +of a series of plant +zones that mark the +decreasing influence +of the factor concerned, +by their +change of character +as they recede from +its point of greatest +intensity. Starting +from a barren, exposed hilltop, for example, with a covering +of dry broom sedge (<i>Andropogon</i>) and fleabane, we encounter +next an almost desert zone of washed and gullied slopes in +whose hard, sunbaked soil nothing but a few scrub pines and +brambles can gain a foothold. This will, perhaps, be succeeded, +by a straggling belt of sassafras, sumac, and buckthorn, mixed +with cat brier and blackberry canes, beyond which, at the foot +of the hill, begins a stretch of meadow, or a bit of woodland +crossed by a brook, or hollowed into a boggy depression. +From this new factor originates a second series of zonations, +passing through all the stages of bog, swamp, shade, and sun<span class="pagenum" id="Page_289">[Pg 289]</span> +plants, back to the prevailing type of the region. Moisture +is really the controlling factor in both cases, its influence +in the first being negative,—that is, inversely,—and in the +other, positive, or directly proportioned to the quantity +present.</p> + +<p id="p-326"><b>326. Direction of zonation.</b>—When the direction in which +the controlling factor changes is horizontal, as with soil and +water, the zonation will be <em>horizontal</em>; when, as in the case +of light, it is vertical, the zonation or stratification will be +<em>vertical</em>. Examples of this can be observed in the growth of +almost any forest area, the natural order of succession being: +(1) a ground layer of mosses and fungi; (2) low, creeping +vines,—partridge berry, trailing arbutus, twinflower (<i>Linnæa</i>); +(3) small ferns and low flowering herbs—pyrola, clintonia, +trillium; (4) a zone of tall herbs and low bushes—royal +fern, cohosh (<i>Actæa</i>), blueberries; (5) tall herbs and shrubs, +small trees, and climbing vines—kalmia, dogwood, farkleberry, +smilax, Virginia creeper; (6) tall treetops towering up +into full sunlight.</p> + +<p>When the physical cause of intensity is a central area, such +as a pond or a hilltop, the zonation will be <em>concentric</em>; that is, +the different belts will succeed each other in widening circles +more or less complete. Where the controlling cause extends +in a line, as a river, or a chain of mountains, the zones run in +parallel belts on each side of it, and the zonation is <em>bilateral</em>. +In any case, however, it is seldom regular, being frequently +broken and interrupted through the intervention of other +factors. Nor must precisely the same kind of plants be +always looked for in similar situations, though their place is +usually occupied by kindred species and genera. The common +pitch pine, for instance, of the Northern sand barrens +is represented in sandy districts farther south by the tall, +long-leaved pine, a kindred species.</p> + +<p id="p-327"><b>327. Succession.</b>—Zonation is a regular succession of +different kinds of plants in space; there is also an analogous +succession in time, as, when the vegetation of a locality is<span class="pagenum" id="Page_290">[Pg 290]</span> +killed off by fire or other cause, plants of an entirely different +character will nearly always spring up to occupy its place. A +forest of pine, for instance, +is rarely followed +by conifers, +but by a growth of +hardwood trees, and +<i>vice versa</i>—nature +thus giving an impressive +example as +to the effectiveness +of a rotation of crops.</p> + +<figure class="figcenter illowp70" id="i_300" style="max-width: 50em;"> + <img class="w100" src="images/i_300.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 423.</span>—A thicket of pines that has succeeded +a mixed growth of hard wood trees.</p></figcaption> +</figure> + +<p>Succession may be +influenced by a variety +of causes. Two +of the most efficient are: (1) the exhaustion of the soil by the +long-continued growth of one formation <a href="#p-60">(60)</a>, thus causing +a deficiency of mineral material suited for the support of +plants of that kind; (2) the migration of new species into +the denuded territory where those which have different requirements +as to mineral +nutrients from the +former inhabitants will, +other things being equal, +have the best chance to +succeed.</p> + +<figure class="figcenter illowp60" id="i_300a" style="max-width: 50em;"> + <img class="w100" src="images/i_300a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 424.</span>—A successful invasion—Japanese +honeysuckle covering the banks of a ravine and +climbing over shrubs and tree tops.</p></figcaption> +</figure> + +<p id="p-328"><b>328. Invasion.</b>—A +rapid and widespread +occupation of any territory +by a new species is +called an <em>invasion</em>. Notable +examples of invaders +are those of the +Russian thistle in the +northwestern states of the Union, and the “bitterweed” +(<i>Helenium tenuifolium</i>) that has almost driven out the hardy<span class="pagenum" id="Page_291">[Pg 291]</span> +dog fennel (<i>Anthemis cotula</i>) which formerly held undisputed +possession of arid places throughout the South Atlantic states. +A still more remarkable instance is the invasion of the Japanese +honeysuckle (<i>Lonicera Japonica</i>), originally introduced +for ornament, but which has naturalized itself within the last +thirty years and overrun waste places everywhere, from the +Gulf to the Potomac, with a vigor and luxuriance equaled +by few of our native species. As its beauty and fragrance +are even more conspicuous in a state of nature than under +cultivation, and as it can, <a id="tn_291">moreover</a>, be made very useful in +stopping gullies and washes, its phenomenally rapid occupation +of so large a territory has caused no alarm and +consequently attracted little attention.</p> + +<p id="p-329"><b>329. Climatic zones.</b>—These are more general groupings +than those we have been considering. They follow +in a rough way the parallels of latitude, and are classed +accordingly as: (1) tropical; (2) subtropical; (3) temperate; +(4) boreal or (on mountains) subalpine; (5) arctic or (on +high mountains) alpine. Taking the cultivated plants of +our own country by way of illustration, we have the subtropical +zone, embracing Florida and the southern portion +of the Gulf states, where sugar cane, rice, and tropical +fruits are the staple crops. Then comes the temperate +zone, with three agricultural subdivisions: (<i>a</i>) the great +cotton belt, with Indian corn, sweet potatoes, and the +peach, melon, and fig as secondary products. Farther +north, in the Central and Middle Atlantic states, we find +(<i>b</i>) the region of maize, hemp, and tobacco, with grapes, +apples, pears, cherries, and a great variety of garden vegetables +as side crops. Finally comes (<i>c</i>) the great wheat-growing +region of the North, with buckwheat, hay, and Irish +potatoes as subsidiary crops.</p> + +<p>Technically, the distribution of the natural zones of vegetation +from south to north is classed under the three general +heads of Forest, Grass Land, and Arctic Desert, with numerous +subdivisions in each.</p> + +<p><span class="pagenum" id="Page_292">[Pg 292]</span></p> + +<p id="p-330"><b>330. Boundaries of the zones.</b>—While the broad continental +zones of vegetation follow, in a general way, the +climatic zones outlined above, they are not sharply defined, +but run into each other and overlap in various degrees, so +that a map depicting the range of vegetation in any wide +area would show a marked deviation from those of latitude. +Various other geographical factors, such as mountain ranges +and bodies of water, influence the direction and character of +the prevailing winds and rains, and through them the moisture +and temperature, to so great an extent that they become +the controlling factors over wide areas. In countries bordering +on the sea, the coast line always marks a belt of its own, +and on the sides of a mountain range, all the climatic zones +from the equator to the pole may be repeated during an +ascent of a few miles.</p> + +<p>In our own country, where the mountain chains and coast +lines run approximately north and south, the great continental +zones have been superseded, for all practical purposes, +by four regional divisions running almost at right angles to +them. These are, disregarding minor subdivisions:—</p> + +<p>(1) The Forest region, occupying the eastern and south +central portion of the Union. In classifying this territory +as forest, it is not meant to imply that it is now, or ever +was, one unbroken jungle, like parts of central Africa, but +that it combines the conditions most favorable to a vigorous +and varied forest growth.</p> + +<p>(2) The Plains region, extending from the very irregular +western boundary of the forest region to the Rocky Mountains.</p> + +<p>(3) The Rocky Mountain region, including the Rockies +and the Sierra Nevadas with the desert area between them.</p> + +<p>(4) The Pacific Slope, a narrow strip between the Sierras +and the Pacific Ocean.</p> + +<p><span class="pagenum" id="Page_293">[Pg 293]</span></p> + +<figure class="figcenter illowp56" id="i_303" style="max-width: 75.0em;"> + <img class="w100" src="images/i_303.jpg" alt=""> + <figcaption><p><span class="smcap">Plate 15.</span>—This giant tulip tree is a relic of the primitive forest. It is twenty-seven +feet in circumference, at a distance of four feet from the ground. Notice the +sharp elbows of the large boughs, a mode of branching characteristic of this kind of +tree.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_294">[Pg 294]</span></p> + +<p>The boundaries of these regions, like those of the great +continental zones, overlap in various ways, the plants of one +region often appearing in another, like an arm of the sea +projecting into the land. But the district where any class of +plants reaches its highest development is its proper habitat, +and as a general thing the one where its cultivation pays +best. It would be a waste of time and money to try to raise +cotton in Maine, or cranberries in Georgia.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Does the native wild growth of a region furnish any indication of +the kind of crops which could be successfully grown there? (<a href="#p-325">325</a>, <a href="#p-326">326</a>.)</p> + +<p>2. Can you give a reason why the zones of cultivation may, in some +cases, be more extensive than the natural range of wild plants in the same +region? (<a href="#p-262">262</a>, <a href="#p-265">265</a>.)</p> + +<p>3. Can you give reasons why the reverse may sometimes be true? (<a href="#p-261">261</a>, +<a href="#p-284">284</a>.)</p> + +<p>4. What crops are raised in different parts of your own state?</p> + +<p>5. Name some of the native plants characteristic of different parts of +your state. What are its principal plant formations?</p> +</div> + + +<h4 id="CH_IX_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>1. Ecology offers the most attractive subject for field work of all the +departments of botany. It can be studied anywhere that a blade of vegetation +is to be found. In riding along the railroad, there is an endless +fascination in watching the different plant societies succeed one another +and noting the variations they undergo with every change of soil or climate.</p> + +<p>2. Students in cities can find interesting subjects for study in the vegetation +that springs up on vacant lots, around doorsteps and area railings, +and even between the paving stones of the more retired streets. On a +vacant lot near the public library in Boston, over thirty different kinds +of weeds and herbs were found, and in the heart of Washington, D.C., on +a vacant space of about twelve by twenty feet, nineteen different species +were counted. Just where such things come from, how they get into +such positions, and why they stay there, will be interesting questions for +city students to solve.</p> + +<p>3. But the country always has been and always will be the happy hunting +ground of the botanist. All the factors considered in the two preceding +sections can hardly be found in any one locality, but by selecting +areas traversed by brooks, or by gullies and ravines, very marked changes +in the character of vegetation may often be observed. Barren, sandy, +or rocky soils, the sunbaked clay of naked hillsides, and the borders of +treeless, dusty roads will offer close approximations to xerophyte conditions.</p> + +<p><span class="pagenum" id="Page_295">[Pg 295]</span></p> + +<p>4. If there are any bodies of water in your neighborhood, examine their +vegetation and see of what it consists. Notice the difference in the shape +and size of floating and immersed leaves and account for it. Note the general +absence of free-swimming plants in running water, and account for it. +Note the difference between the swamp and border plants and those growing +in the water, and what trees or shrubs grow in or near it. Compare +the vegetation of different bogs and pools in your neighborhood, and +account for any differences you may observe. Compare the water plants +with those growing in the dryest and barrenest places in your vicinity, +note their differences of structure, and try to find out what special adaptations +have taken place in each case. Make a list of those in each location +examined that you would class as pioneers.</p> + +<p>5. Draw a map of the vegetation of some locality in your neighborhood +that presents a variety of conditions, such as a steep hillside, a field or +meadow traversed by a brook, the slopes and borders of a ravine, or the +change from cultivated ground to uncultivated moor or woodland. Represent +the different zones and formations by different colored inks or crayons, +or by different degrees of shading with the pencil.</p> + +<p>6. Draw a map of your state showing the different agricultural regions, +as indicated by the character of the cultivated plants in each; +use different colors, or light and dark shading, to define the boundaries. +Notice any irregularities of outline and account for them—whether due +to soil, moisture, geological formation, winds, or temperature. What is +the controlling factor of each region?</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_296">[Pg 296]</span></p> + +<h2 class="nobreak" id="CH_X">CHAPTER X. CRYPTOGAMS</h2> +</div> + + +<h3 id="CH_X_I">I. THEIR PLACE IN NATURE</h3> + +<p id="p-331"><b>331. Order of development.</b>—All the forms that have +hitherto claimed our attention belong to the great division +of Spermatophytes, or seed-bearing plants, designated also as +<em>Phanerogams</em>, or flowering plants. They comprise the higher +forms of vegetable life, and because they are more conspicuous +and better known than the other groups, they have been +taken up first, since it is more convenient, for ordinary purposes, +to work our way backward from the familiar to the less +known, rather than in the reverse order.</p> + +<p>But it must be understood that this is not the order of +nature. The geological record shows that the simplest +forms of life were the first to appear, and from these all the +higher forms were gradually evolved. There is no sharp +line of division between any of the orders and groups of +plants, but the line of development can be traced through a +succession of almost imperceptible changes from the lowest +forms to the highest, and it is only by a study of the former +that botanists have come to understand the true nature and +structure of the latter.</p> + +<p id="p-332"><b>332. Basis of distinction.</b>—<em>Cryptogams</em>, or seedless +plants as a whole, are distinguished from the phanerogams +by their simpler structure and by their mode of propagation, +which in the former is by means of spores, while in the +phanerogams it is by seeds. A spore is a simple organic +body, consisting usually of a single cell which separates from +the parent plant at maturity and gives rise to a new individual. +A seed is a complicated, many-celled structure, containing +within itself the rudimentary structure of a new plant already +organized.</p> + +<p><span class="pagenum" id="Page_297">[Pg 297]</span></p> + +<p>Beginning with the simplest forms, cryptogams are grouped +in three great orders:—</p> + +<p id="p-333"><b>333. I. Thallophytes</b>, or thallus plants.—This group takes +its name from the <em>thallus</em> structure that characterizes its +vegetation. In its typical form, a thallus is +a more or less flat, expanded body, of which +the lichens and liverworts offer familiar examples +among land plants, and the kelps and +laminarias among seaweeds. It may be of +any size and shape, however, and sometimes +consists of a mere filament, as in the common +brook silk, or even of a single cell (<a href="#i_310">Fig. +429</a>). The term is applied in general to the +simplest kinds of vegetable structure, in +which there is no differentiation of tissues, +and no true distinction of root, stem, and +leaves. While it is not peculiar to the thallophytes, +it has attained its most typical development among +them, and the name is therefore retained as distinctive of +that group. It embraces two great divisions, +the Algæ and Fungi. The first +includes seaweeds and the common freshwater +brook silks and pond scums, besides +numerous microscopic forms whose +presence escapes the eye altogether, or is +made known only by the discolorations +and other changes caused by them in the +water. To the fungi belong the mushrooms +and puffballs, the molds, rusts, +mildews, and the vast tribe of microscopic +organisms called <em>bacteria</em>, which +are so active in the production of fermentation, putrefaction, +and disease.</p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp45" id="i_307" style="max-width: 15em;"> + <img class="w100" src="images/i_307.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 425.</span>—A seaweed +with broad, expanded +thallus.</p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp45" id="i_307a" style="max-width: 15em;"> + <img class="w100" src="images/i_307a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 426.</span>—Anthoceros, +a liverwort with flat, +spreading thallus.</p></figcaption> +</figure></td></tr></table> + +<p id="p-334"><b>334. II. Bryophytes</b>, or moss plants.—This group likewise +contains two main divisions, Mosses and Liverworts. Familiar +examples of the latter are the flat, spreading green plants, +<span class="pagenum" id="Page_298">[Pg 298]</span> +bearing somewhat the aspect of lichens, met with everywhere +on wet rocks and banks around shady watercourses. The +name is a reminiscence of their former use +in medicine as a specific for diseases of the +liver, and not, as in the case of the liver leaf, +of a fancied resemblance to that organ.</p> + +<p>Mosses are one of the best defined of +botanical orders, and are easily recognized +by their slender, leafy fruiting stalks, growing +usually in dense, spreading mats, and +presenting every appearance of a highly +organized structure, well differentiated into +root, stem, and leaves.</p> + +<p>The liverworts represent +the more primitive division +of the group, and in some +of their forms approach so +near the thallophytes that +it is not difficult to recognize +them as connecting +links in the same chain of +life. Their relationship to the next higher +group is not clear, but while they represent +a more primitive stage of evolution than +the mosses, the development of the latter +has followed a course divergent from the +main line of evolutionary progress.</p> + +<table class='autotable'> +<tr><td class='vab'> +<figure class="figcenter illowp45" id="i_308" style="max-width: 25em;"> + <img class="w100" src="images/i_308.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 427.</span>—A +shoot of peat moss +with ripe spore +fruits, <i>f</i>, <i>f</i>.</p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp45" id="i_308a" style="max-width: 25em;"> + <img class="w100" src="images/i_308a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 428.</span>—A common +fern (<i>Polypodium +vulgare</i>).</p></figcaption> +</figure></td></tr></table> + +<p id="p-335"><b>335. III. Pteridophytes</b>, or fern plants, are +classed roughly in the three divisions of +ferns, horsetails, and club mosses. They +differ greatly in structure, but all possess a +vascular system, and a well-organized structure +of root, stem, and leaves. They rank +next to the spermatophytes in the order of +development, and the group is of especial interest on account +of its relationship to the higher plants. One of its divisions,<span class="pagenum" id="Page_299">[Pg 299]</span> +the club mosses, has probably given rise to at least one section +of the gymnosperms, while the ferns are regarded as the +ancestors of the true flowering plants, which make up the +great class of angiosperms, and represent the highest type of +evolution yet attained in the vegetable kingdom.</p> + + +<h3 id="CH_X_II">II. THE ALGÆ</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Simple forms of green algæ can be found on the shady +side of tree trunks, damp walls, old fence palings, and the outside of flowerpots. +<i>Pleurococcus</i>, one of the commonest kinds, occurs as a green, +powdery mat or felt in damp places, and is often accompanied by <i>protococcus</i>, +another good specimen for study. <i>Spirogyra</i> and other filamentous +algæ can be found in stagnant pools and ditches and in old rain barrels.</p> + +<p><span class="smcap">Appliances.</span>—Eosin solution, nitric acid, alcohol, iodine solution; +a white china plate; a hand lens; a compound microscope, and slides.</p> +</div> + +<p id="p-336"><b>336. Variety of forms.</b>—This group embraces plants of +the greatest diversity of form and structure, from the minute +volvox and desmids that hover near the uncertain boundaries +dividing the vegetable from the animal world, to the giant +kelps of the ocean, which sometimes attain a length of from +six hundred to one thousand feet. They are usually classed +according to their color, as green, brown, and red algæ, +including various subdivisions of each group. They all contain +chlorophyll, by means of which they manufacture their +own food, though in the red and brown divisions it is masked +by the presence of other pigments—an adaptation to the +modified light that reaches them at various depths under +water. With few exceptions they can live only in the water, +and unlike any other form of plant life, attain their highest +development in the salty depths of the ocean. The freshwater +forms are small and inconspicuous, and generally of a +more simple type than the seaweeds. The great majority of +them belong to the two classes of green and blue-green algæ. +The former is believed to have furnished the type from +which the higher plants have been evolved.</p> + +<figure class="figright illowp40" id="i_310" style="max-width: 20em;"> + <img class="w100" src="images/i_310.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 429.</span>—Three stages in +the division of a one-celled alga +(<i>Glœocaspa polydermatica</i>): <i>A</i>, +division of a cell just beginning; +<i>B</i>, division further advanced; +<i>C</i>, four cells after division, remaining +in contact.</p></figcaption> +</figure> + +<p id="p-337"><b>337. Study of a one-celled alga.</b>—Put a little of the green +algæ in water on a glass slide. Hold up to the light, or<span class="pagenum" id="Page_300">[Pg 300]</span> +over a sheet of white paper, and examine with a hand lens; +then place under the microscope. It will probably be found +to contain a number of minute organisms, but the pleurococci +can be recognized as small round bodies of a bright green +color, some of them separate, others adhering together in +groups of two, four, or more, with the sides that are in contact +slightly flattened. Each of these bodies is an individual +plant consisting of a single cell, whence they are said to be +<em>unicellular</em>. Draw one of the single cells and one of the +groups, or colonies, as they appear +under the microscope. Try to make +out the cell wall and the nucleus, and +label all the parts (see 7). If you +have any difficulty in distinguishing +the cell wall, drop a little glycerine +or salt water on the slide. This will +cause the cell contents to shrink by +osmosis (56, 59). Can you make +out the structure of the cell colonies? +They have resulted from the peculiar +mode of multiplication that prevails +among this class of plants. A cell +elongates, contracts in the middle, +and divides into two parts, each of +which becomes an independent plant like the mother cell. +See if you can find one in the process of division. The +daughter cells repeat the process, each one giving rise to two +new individuals, and so on indefinitely. The new cells do +not always separate immediately on their formation, but frequently +adhere together for a time, in colonies, before falling +away and beginning an independent existence.</p> + +<p id="p-338"><b>338. Reproduction by fission.</b>—This kind of reproduction +is called <em>fission</em>, or cell division, and marks a very primitive +stage of development. Under stress of adverse conditions +the cells formed by division may remain inactive for a time. +They are then called <em>resting spores</em>, and when more favorable<span class="pagenum" id="Page_301">[Pg 301]</span> +circumstances arise, they begin again their work of reproduction +and growth as actively as ever.</p> + +<p id="p-339"><b>339. Meaning of the name.</b>—The suffix <em>coccus</em> is a Latin +noun (plural <em>cocci</em>) meaning a grain or berry, and is a general +term applied to any small, round organism consisting of a +single cell; hence, <em>micrococcus</em>, a minute round body; <em>protococcus</em>, +a primitive form, or prototype of one-celled bodies; +and <em>pleurococcus</em>, which may be freely translated “a one-sided +little round body,” from the flattening of the adjacent +sides during fission—<em>pleuro</em> meaning lateral, or pertaining +to the side.</p> + +<p>It is important to remember this definition, as the term +<em>coccus</em> is of very frequent occurrence in works of biology, as a +suffix for designating small round bodies of various kinds.</p> + +<p id="p-340"><b>340. Examination of a filamentous alga.</b>—Place on a +white dish a few drops of water containing some of the green +pond scum common in stagnant pools and ditches. Examine +with a hand lens; of what does it appear to consist? +Are the filaments all alike, or are they of different lengths +and thickness? Soak a number of them in alcohol for half +an hour and examine again; where has the green matter +gone? Do these algæ contain chlorophyll? (<a href="#p-336">336</a>; <a href="#exp-65">Exp. 65</a>.) +This class are called filamentous algæ on account of their +slender, threadlike thalli, which look like bits of fine floss +floating about in the water. The bubbles of oxygen which +they sometimes give off in great abundance cause the +frothy appearance that has given rise to their popular +name, “frog spit.”</p> + +<figure class="figright illowp45" id="i_312" style="max-width: 19em;"> + <img class="w100" src="images/i_312.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 430, 431.</span>—<i>Spirogyra</i> +(magnified): 430, +two filaments beginning +to conjugate; 431, formation +of spores.</p></figcaption> +</figure> + +<p id="p-341"><b>341. Spirogyra.</b>—The filamentous algæ are very numerous, +and a drop of pond scum will probably contain several +kinds. At least one of these, it is likely, will be a <i>Spirogyra</i>, +as this is one of the commonest and most widely +distributed of them all. Place a filament under the microscope +and notice the spiral bands in which the chlorophyll +is disposed within the cells. It is from this spiral arrangement +that the species takes its name. Do you notice any<span class="pagenum" id="Page_302">[Pg 302]</span> +roundish particles inclosed in the chlorophyll bands? Test +with a little iodine solution and see what they contain. +Each filament will be seen, when sufficiently magnified, +to consist of a number of more or less cylindrical cells joined +together in a vertical row, and thus forming the simple +threadlike thallus which characterizes this +class of algæ. Physiologically, each cell +is an independent individual, and often +exists as such. Can you see the cell +nucleus? If not, place a few filaments +in a solution of eosin and add a drop of +acetic acid to give the solution a pale +rose color. After twenty to thirty minutes, +examine again; the nucleus will be +stained a deep red. If you can find an +unbroken filament, examine both ends to +see whether there is any differentiation of +base and apex.</p> + +<p id="p-342"><b>342. Conjugation.</b>—See if you can find two filaments +sending out lateral protuberances toward each other. +Watch and notice that after a time these projections come +together and unite by breaking down the cell walls dividing +them, the protoplasm in each contracts, the contents of +one pass over into the other, and the two coalesce, forming +a new cell but little, if any, larger than the original conjugating +bodies. This cell germinates under favorable +conditions and produces a new individual. This method +of reproduction is known as <em>conjugation</em>. The cells thus produced +by the union of the contents of two separate cells +may either germinate at once, and give rise to new individuals, +or remain quiescent for a time, as resting spores.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Are any of the green algæ parasitic? How do you know? (<a href="#p-186">186</a>, +<a href="#p-336">336</a>.)</p> + +<p>2. Why is their presence in water regarded as denoting unhygienic +conditions?</p> + +<p><span class="pagenum" id="Page_303">[Pg 303]</span></p> + +<p>3. Mention some of the ways in which their presence may contribute +to the contamination of drinking water.</p> + +<p>4. Refer to <a href="#exp-66">Exp. 66</a>, and account for the bubbles and froth that usually +accompany these plants in the water.</p> + +<p>5. Can you suggest any other causes than the evolution of oxygen that +might produce the same effect?</p> + +<p>6. Is the presence of these gas bubbles of any use to floating plants?</p> +</div> + + +<h3 id="CH_X_III">III. FUNGI</h3> + +<figure class="figright illowp50" id="i_313" style="max-width: 37em;"> + <img class="w100" src="images/i_313.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 432.</span>—A common form of mold, magnified, +showing thallus modified into a fibrous mycelium: +<i>a</i>, <i>a</i>, spore cases; <i>b</i>, mycelium. (<i>After</i> <span class="smcap">Kopf</span>, in part.)</p></figcaption> +</figure> + +<p id="p-343"><b>343. Classification.</b>—In the fungi the thallus structure +is greatly modified, appearing usually as a network of fine +threads called the <em>mycelium</em> +(pl., <em>mycelia</em>), from a Greek +word meaning “fungus” +<a href="#p-369">(369)</a>. These plants are +all, with a few doubtful +exceptions, parasites or +saprophytes which contain +no chlorophyll and are +incapable of supporting an +independent existence. +Biologists are divided as to +their position in the genealogical +tree of life. The +weight of authority +at present inclines to +the view that they are +degenerate forms derived +from the algæ, +but they have been +so modified by their +parasitic habits as to +render their position +in the general scheme of life a doubtful one. They represent +an offshoot, or side branch, as it were, of the great +evolutionary line, and so may be considered for the present +as standing apart in a class by themselves.</p> + +<p><span class="pagenum" id="Page_304">[Pg 304]</span></p> + +<p id="p-344"><b>344. Numbers and variety.</b>—Fungi exceed every other +class of living organisms both in the number of species and +of individuals composing them. They include such diverse +forms as bacteria, molds, rusts, mildews, mushrooms, and +the like, ranging in size all the way from the giant puffball, +a foot or more in diameter, to the almost inconceivably +minute influenza bacillus, of which nearly two thousand +million can inhabit a single drop of water without inconvenient +crowding!</p> + +<figure class="figcenter illowp100" id="i_314" style="max-width: 100em;"> + <img class="w100" src="images/i_314.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 433.</span>—Cephalothecium, a fungus parasitic on rosehips—greatly magnified. +(<i>From</i> Mo. Botanical Garden Rep’t. Photographed by Hedgcock.)</p></figcaption> +</figure> + +<p id="p-345"><b>345. The parasitic habit.</b>—But while their life history +is obscure and hard to trace, the fungi are, as a class, well +differentiated by their parasitic habit. They contain no +chlorophyll, can manufacture no food, and consequently +have to obtain it ready-made from the tissues of living or +dead animals and plants. On this account they are active +agents in the production of disease and decay, especially +certain of those manifold forms that have been grouped<span class="pagenum" id="Page_305">[Pg 305]</span> +together under the general head of bacteria. While not responsible +for all the disease known to be caused by living +organisms,—some very serious ones, such as malaria and +cattle fever, being due to animal parasites,—the majority of +those that have been most carefully investigated are traced +to the bacteria, or other fungi. After any of these parasites +have found a lodgment in the body of an organism whose +tissues furnish them a congenial habitat, they multiply with +enormous rapidity, and through the action of certain poisons +called <em>toxins</em>, which they excrete, give rise to the most destructive +diseases in both animals and plants; and no rational +sanitary science is possible without a knowledge of their +habits and life history. Add to the vast amount of human +suffering that is to be laid at their door the economic damage +done by rust and smut fungi, by molds and blights and mildews, +and we shall be tempted to conclude that the “battle +of life” is largely a struggle against these invisible foes.</p> + +<figure class="figcenter illowp100" id="i_315" style="max-width: 99em;"> + <img class="w100" src="images/i_315.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 434-437.</span>—Disease-producing bacteria: 434, bacteria of consumption +(<i>Bacillus tuberculosis</i>); 435, cholera bacillus; 436, bacilli of anthrax, showing spores; +437, typhoid bacillus.</p></figcaption> +</figure> + +<p id="p-346"><b>346. Useful fungi.</b>—Not all fungi, however, are injurious. +On the contrary, the great majority of them are harmless, +and very many kinds are positively beneficial to man. +Without the yeasts and bacteria of fermentation we could +not have our bread and cheese. Other forms are active +agents in the fertilization of soils, it having been estimated +that there are 100,000 or more of these infinitesimal laborers +at work in every cubic centimeter (about ¹⁄₁₆ of a +cubic inch) of virgin soil! Even the bacteria of putrefaction, +which we are accustomed to regard as the embodiment<span class="pagenum" id="Page_306">[Pg 306]</span> +of all that is foul and loathesome, are engaged in an unceasing +work as scavengers, without which life would no longer +be possible on our globe, as will be shown in the following +section.</p> + + +<h4 id="CH_X_III_A">A. <span class="smcap">Bacteria</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A vessel of water in which hay has been left to soak for +several hours; a freshly boiled potato.</p> + +<p><span class="smcap">Appliances.</span>—A double boiler for sterilizing; a number of clean glass +jars and bottles; cotton wool for stoppers; a compound microscope.</p> + +<p><span class="smcap">Culture Mediums.</span>—A freshly boiled potato answers very well for +ordinary purposes. “Bread mash” can be made by drying some bread +crumbs in an oven, then mashing and mixing them to a paste with boiling +water; sterilize by three successive heatings in a double boiler. A sterilized +preparation of gelatine solution is the medium most commonly used.</p> +</div> + +<p id="p-347"><b>347. How to obtain specimens for observation.</b>—While +bacteria are plentiful almost everywhere, it is not always +easy to capture them just when and where you want them. +For this purpose, put some hay in water and leave in a +warm place away from the light until the liquid becomes +cloudy or a film forms on the surface. This will show that +bacteria are present. If it is desired to study any particular +kind of bacterium, inoculate one of the culture mediums +described under “material,” or a few drops of sterilized +extract of beef, with a small quantity of the substance to be +examined, or with dust or scrapings from the locality under +consideration.</p> + +<div class="blockquot"> + +<p id="exp-93"><span class="smcap">Experiment 93. By what means are bacteria commonly distributed?</span>—Put +a slice of freshly boiled potato into each of three glass tumblers +and cover with a filter of cotton wool held in place by tying tightly +with a cord, or by an elastic band. Set them all in a vessel of water, bring +it to a boil, and keep at that temperature for half an hour, to sterilize the +air in the tumblers. When they have cooled, lift the cotton from (1) for +a minute or two and then replace. Carefully pass the tip of a medicine +dropper through the filter of (2) so as to prevent the entrance of unsterilized +air, and put on the slice of potato a small quantity of the bacterial +liquid prepared as directed in the last paragraph. Leave (3) unopened. +Keep all together in a warm, dark place and observe at intervals of from +12 to 24 hours. Do any bacteria appear in (3)? Do any appear on the<span class="pagenum" id="Page_307">[Pg 307]</span> +potato in (2), where the liquid was dropped? Are they more, or less +abundant than in (1)? Since cotton wool is entirely impervious to the +smallest microörganisms known, would you judge from this experiment +that bacteria can get into any place unless carried there by the air, or by +some other means?</p> + +<p id="exp-94"><span class="smcap">Experiment 94. Can bacteria be carried by pure air?</span>—On a +warm (and preferably cloudy) day, put a slice of potato on a plate, and +leave uncovered in an unused room or closet, free from dust, and kept +carefully closed. Put another slice arranged in exactly the same way +in an open window on a dusty street, or in a room that is used and daily +swept and dusted. Do bacteria appear in the first plate? In the second? +Is air free from dust a good conveyor of bacteria?</p> + +<p id="exp-95"><span class="smcap">Experiment 95. What conditions are favorable to bacterial +growth?</span>—Strain some of your culture liquid into half a dozen small +bottles of the same size, filling each about half full. Put (1) in a dark, +cool place—on ice, if the weather is warm; (2) in a dark, warm place; +(3) in a warm, well-lighted place; into (4) put a drop of carbolic acid, formalin, +corrosive sublimate, or boracic acid, and keep in a dark, warm place. +Keep (5) in boiling water for half an hour or more, and then place beside +(2). Keep (6) in a freezing mixture of salt and ice for several hours, then +place with (2) and (5). Examine all at intervals of from 12 to 24 hours. +In which bottles is the presence of bacteria indicated by cloudiness of the +contained liquid, or the formation of a surface film? In which do they +appear first? In which most abundantly? In which last, or not at all? +What is the effect of light and darkness on their growth? Of heat and +cold? Of disinfectants? Name the circumstances that tend to hinder +their growth, in the order of their efficacy.</p> +</div> + +<p id="p-348"><b>348. Microscopic study of bacteria.</b>—Put a drop of +hay infusion on a slide and examine with the highest power +of the microscope. You will see a multitude of very small +glistening bodies including different kinds of bacteria, a +majority of which are probably the hay bacillus, <i>B. subtilis</i>, +shown in <a href="#i_319">Figs. 443, 444</a>. Notice that some forms +move about freely, while others are non-motile. Which +kind are the more numerous? The motion may be either mechanical, +resembling that of the small dust particles we see +dancing about in the sunshine, or apparently voluntary, +and caused by the vibration of little whiplike cilia. Can +you distinguish the two kinds? Try to make out clearly<span class="pagenum" id="Page_308">[Pg 308]</span> +the different shapes you see. Some appear as slender +chains or filaments, but this is due to the individual cells’ +adhering together for a time before breaking up and beginning +an independent existence. The small, rounded bodies, +like a period (<a href="#i_318">Fig. 438</a>), are <em>cocci</em>; the slender, rod-shaped +ones—sometimes slightly curved (<a href="#i_318">Fig. 440</a>)—are <em>bacilli</em> +(sing., <em>bacillus</em>); the comma-shaped ones, and those generally +showing a slight spiral curvature, are <em>vibrios</em> (<a href="#i_318">Fig. +441</a>); the spirally twisted ones, like a corkscrew (<a href="#i_318">Fig. 442</a>), +are <em>spirilli</em> (sing., <em>spirillum</em>). These are the principal forms +which it is important to distinguish and remember. The +names are applied very loosely, however, in practice, bacillus +being often used as a general term applicable to almost any +kind,—the spirillum of cholera, for instance, being commonly +known as the cholera bacillus, while by some authors +vibrios are ranked as a variety of spirillum.</p> + +<figure class="figcenter illowp100" id="i_318" style="max-width: 50em;"> + <img class="w100" src="images/i_318.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 438-442.</span>—Typical forms of bacteria: 438, coccus type; 439, the same, +hanging together in chains; 440, rod-shaped bacteria (bacillus type), the clear areas +in some of these are spores; 441, forms of vibrio; 442, forms of spirillum.</p></figcaption> +</figure> + +<p id="p-349"><b>349. Life history of a typical bacterium.</b>—A pure culture +of the <i>Bacillus subtilis</i> can easily be obtained by boiling +some of the hay infusion for half an hour and then leaving<span class="pagenum" id="Page_309">[Pg 309]</span> +in a warm place till the usual indications of the presence +of bacteria appear <a href="#p-347">(347)</a>. The spores of this micro-organism +are so resistant that they can withstand the temperature +of boiling water for several hours, while those of +most other forms of bacteria are killed by a few minutes’ +exposure to it; hence, the crop that develops after boiling +will consist of a pure culture of the +hay bacillus.</p> + +<figure class="figright illowp45" id="i_319" style="max-width: 31.25em;"> + <img class="w100" src="images/i_319.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 443, 444.</span>—Hay bacillus (<i>B. subtilis</i>): +443, a portion of the film from the culture +liquid, the black lines, <i>e</i>, being bacteria +in the vegetative state; 444, spore formation; +<i>a</i>, <i>d</i>, motile cells and chain of cells: <i>b</i>, +non-motile cells; <i>c</i>, spores and chain of +spores from the film <i>e</i>.</p></figcaption> +</figure> + +<p>In their active state these organisms +will be seen to consist of single-celled, +rod-shaped bodies, about +three or four times as long as broad, +and generally cohering in +bands or filaments, as shown +in <a href="#i_319">Fig. 444</a>, <i>c</i>. The black dots +within the cells are the +spores. Each individual +bacterium produces but a +single spore, or rather becomes +a spore itself, by the +contraction of its contents +and the formation around +them of a strong inclosing +membrane. On germinating, +the spores give rise to +little ciliated, one-celled organisms +called “swarm +spores,” that swim about +freely in the containing medium and multiply rapidly for a +time by cell division. After this they pass again into the +quiescent state, ready, whenever favorable conditions arise, +to begin anew the repetition of their life cycle, which is an +irregular alternation of cell division and spore formation.</p> + +<p id="p-350"><b>350. Resistance of spores.</b>—Bacteriologists are not fully +agreed as to the cause of spore formation, some holding +that it takes place only when conditions are most favorable<span class="pagenum" id="Page_310">[Pg 310]</span> +for bacterial growth, others claiming the reverse. The +consensus of opinion at present is toward the view that the +spores are a provision for tiding over periods of stress and +difficulty. They are capable of retaining their vitality +for a long time, and are much harder to kill than the bacterial +cells in their ordinary vegetative state, as was seen +in the case of the hay bacillus. The spores of one species +of potato bacillus have retained their vitality after four +hours of boiling, and those of the typhoid bacillus after +continuous exposure to a freezing temperature for more +than three months. The majority of bacteria, in their +vegetative state, are, however, either killed or rendered +inert by temperatures ranging below 10° or above 50° centigrade—equivalent +to about 50° and 122° Fahrenheit, +respectively. It is easy to see what important bearing +these facts have on the process of disinfection.</p> + +<p id="p-351"><b>351. Reproduction and multiplication.</b>—The ordinary +mode of reproduction in bacteria, as in other unicellular +organisms, is by fission (<a href="#p-337">337</a>, <a href="#p-338">338</a>). As each individual +forms but a single spore, no increase in numbers could take +place by this means alone. Hence, while the spores are +an important factor in the preservation of the species by +continuing its existence under conditions which the active +organisms could not survive, their successful propagation +depends on their power of rapid multiplication by division. +If this process were to go on unchecked, every hour, in an +unbroken geometrical progression, the progeny of a single +bacterium would, in 24 hours, number nearly 17 million; +in 25 hours, 34 million; in 26 hours, 68 million, and in five +days they would cover the entire surface of the globe, land +and sea, to a depth of 3 feet! In ordinary standard milk +sold by dairymen, and containing, when examined, less +than 10,000 microbes to the cubic centimeter,—about +20 drops,—the number was found to have increased after +24 hours to 600 million. It is comforting to know, however, +that the majority of these are of the harmless kinds<span class="pagenum" id="Page_311">[Pg 311]</span> +which are the active agents in the making of buttermilk +and cheese.</p> + +<p>The effects of their rapid multiplication will be better +appreciated when we consider that bacteria are the smallest +of known living creatures. If 1000 of the influenza bacilli +were spread out in a single layer with their sides touching, +but not overlapping, they would not take up more room +than one of the periods used in punctuating this book; +and a coccus concerned in a tubercular disease prevalent +among cattle in South America has recently been discovered, +of which double that number could be accommodated in the +same space.</p> + +<figure class="figcenter illowp100" id="i_321" style="max-width: 100em;"> + <img class="w100" src="images/i_321.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 445, 446.</span>—Milk (highly magnified): 445, pure, fresh milk, showing fat +globules; 446, milk that has stood for hours in a warm room in a dirty dish, showing +fat globules and many forms of bacteria.</p></figcaption> +</figure> + +<p id="p-352"><b>352. Distribution of bacteria.</b>—Ordinary air, when free +from dust, contains, on the average, not more than five +germs to the liter—equal to about 1 for every 12 cubic +inches. Pathogenic, or disease-producing, germs seldom +occur in ordinary fresh air, and even when present are, under +ordinary circumstances, harmful only to people whose +bodies, by reason of physical weakness or unhygienic habits, +offer a congenial soil for their multiplication. Numerous instances +are known in which perfectly healthy persons have +carried about infectious disease germs in their bodies and +even transmitted them to others without experiencing +any inconvenience, or even being aware of their presence.<span class="pagenum" id="Page_312">[Pg 312]</span> +Among others, the germs of pneumonia, diphtheria, and +tuberculosis are often found in the mouth, nose, and sputum +of perfectly healthy persons. There are also a number +of bacteria that are regular inhabitants of the mouth, some +of which are the cause of decayed teeth and foul breath. +One form of bacterium, concerned in the production of inflammation +and abscesses (<em>Staphylococcus</em>) is so constantly +present on the human epidermis that one authority has +declared it impossible to sterilize the skin so thoroughly +as to free it entirely of this microbe. It is ordinarily not +harmful unless it comes in contact with open wounds and +abrasions.</p> + +<p id="p-353"><b>353. The economic importance of bacteria.</b>—It is hard +to say whether these organisms concern us most on account +of the damages attributable to them on the one hand, or +the benefits we owe them on the other. If they were all +as harmful as the pathogenic kinds, life would hardly be +possible on the globe, while without their presence life +as we know it would have ceased to be possible long ago. +They are nature’s great army of scavengers, the sole agents +of decomposition, without which dead organic matter would +be subject only to the slow changes by which the rocks +and mineral matter of the earth’s crust are disintegrated, +and the undecomposed bodies of the vast procession of +plants and animals that have existed since life first began +on our globe would long ago have cumbered its surface to such +an extent as to render impossible the continued development +of life such as we know.</p> + +<p id="p-354"><b>354. Sterilization</b> is the process of ridding a substance +of living microörganisms. To do this effectively, the process +must be repeated several times at intervals, so as +to give any spores that may have survived previous applications +time to pass into the vegetative state, when their +power of resistance is diminished and they are more easily +destroyed. The incubation period, as the time required +for the germination of the spores is called, is different for<span class="pagenum" id="Page_313">[Pg 313]</span> +different kinds of bacteria; hence the importance, from a +sanitary point of view, of a thorough knowledge of their life +history.</p> + +<p id="p-355"><b>355. Disinfection</b> is sterilization on a large scale, and +the same principles apply to both. Heat is the safest +disinfectant for objects that will bear it, if continued long +enough and repeated often enough at a sufficiently high +temperature. Freezing will destroy some kinds of germs +and check or retard the development of nearly all, but +is not to be relied on as a permanent germicide, since +even among flowering plants there are many kinds, not +only of seeds, but of perennial vegetative forms that are +capable of enduring an arctic temperature of many degrees +below freezing for long continued periods.</p> + +<p>Chemical disinfectants act usually as microbe poisons, +and are unsuitable as sterilizers for food, though valuable +in the purification of houses, clothing, and utensils—especially +the instruments employed in surgical operations.</p> + +<p>The prevention of the growth of bacteria, especially in +wounds and surgical incisions, whether by means of chemical +or physical agencies, is known as <em>antisepsis</em>.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why should a person recovering from an ague continue for some +time after to take quinine every third or every seventh day? (<a href="#p-350">350</a>, <a href="#p-354">354</a>.)</p> + +<p>2. Name some of the principal diseases produced by bacteria.</p> + +<p>3. What is the principle to be acted on in the avoidance of such diseases? +(<a href="#exp-94">Exps. 94</a>, <a href="#exp-95">95</a>.)</p> + +<p>4. Are the same means equally effective for prevention and for cure? +(<a href="#p-354">354</a>, <a href="#p-355">355</a>; <a href="#exp-93">Exps. 93-95</a>.)</p> + +<p>5. Why is “fresh air” beneficial in a sick room? (<a href="#p-352">352</a>; <a href="#exp-94">Exp. 94</a>.)</p> + +<p>6. Does it act as a disinfectant, or as a mere diluent of the infected +air of the room? (<a href="#p-352">352</a>.)</p> + +<p>7. Why ought preserved fruits and vegetables to be scalding hot when +put into the can? (<a href="#p-355">355</a>.)</p> + +<p>8. Why is it necessary to exclude the air from them? (<a href="#exp-93">Exps. 93</a>, +<a href="#exp-94">94</a>.)</p> + +<p>9. Reconcile question 8 with question 5.</p> + +<p><span class="pagenum" id="Page_314">[Pg 314]</span></p> + +<p>10. Why does the use, for drinking purposes, of water that has been +boiled render a person less liable to infectious diseases? (<a href="#p-355">355</a>.)</p> + +<p>11. Was the old-fashioned practice of handing the baby round to be +promiscuously kissed by friends and neighbors a good one for the baby? +(<a href="#p-352">352</a>.)</p> + +<p>12. Why is the spitting habit to be condemned? The use of common +drinking cups in schoolrooms and other public places? (<a href="#p-352">352</a>.)</p> + +<p>13. Is it proper from a sanitary point of view that roommates at a boarding +school, or even members of the same family, should use soap, towels, +and other articles of the toilet in common? (<a href="#p-352">352</a>.)</p> +</div> + + +<h4 id="CH_X_III_B">B. <span class="smcap">Yeasts</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A piece of fresh baker’s yeast, some warm water, and a +little honey or sugar solution; a pipette, or a medicine dropper; three or +four clean pint bottles or preserve jars.</p> + +<p>To raise a crop of yeast fungi for observation, rub one fourth of a fresh +yeast cake in water enough to make a paste; add one pint of water, with +a tablespoonful of honey or sugar, and stir well.</p> + +<p id="exp-96"><span class="smcap">Experiment 96. What conditions favor the growth of yeast?</span>—Pour +equal parts of the liquid made as directed (see Material) into each +of three pint bottles, stopper lightly, and label. Put (1) in a warm, dark +place; (2) in a cool, dark place; and (3) in a bright light in a warm place. +Observe at intervals of a few hours the changes that occur in each. Notice +the bubbles that rise from the liquid. In which bottle do they form most +rapidly? Lower a lighted match into it, or transfer some of the gas with +a pipette into a vessel containing limewater, and tell what it is. Taste +some of the fermenting liquid. Is it sweet? What has become of the +sugar that was put into it?</p> +</div> + +<p id="p-356"><b>356. Yeasts and ferments.</b>—Yeasts belong to a very different +order of fungi from the bacteria, but on account of +their simplicity of structure and the similarity of their action +to that of some of the latter, it is usual to consider them together. +They are the active agents of fermentation, and +include a large number of species. The kind used for household +purposes is the same as that employed in making beer. +Of this species there are many varieties, each one of which +gives a characteristic taste to the beer made from it; and +brewers, by paying attention to the cultivation of yeasts, +give their product the special flavors peculiar to the different<span class="pagenum" id="Page_315">[Pg 315]</span> +brands. This kind of yeast is not known to exist except in +a state of cultivation, and probably owes its survival and +present condition of development to a symbiosis with man, +on account of its usefulness in bread making, and still more, +perhaps, to its part in the gratification of his bibulous propensities, +for among savage tribes the manufacture of fermented +liquors is practiced long before the wholesome art of +bread making.</p> + +<figure class="figcenter illowp100" id="i_325" style="max-width: 100em;"> + <img class="w100" src="images/i_325.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 447-449.</span>—Forms of common yeast (<i>Saccharomyces cerevisiæ</i>): 447, +brewers’ yeast; 448, household yeast (the large grains are starch); 449, yeast from +beer sediment, showing budding. (Figs. 447, 448 × 250; Fig. 449 × 1270.)</p></figcaption> +</figure> + +<p>There are other yeasts existing in a state of nature, such as +those on the surface of fruits, which cause the latter, under +certain circumstances, to ferment and decay. For this reason +artificial ferments are not needed in making wine and +other alcoholic liquors from fruits. Fermentation is also +caused by certain forms of bacteria, as in the formation of +vinegar and the souring of milk. Such bacteria often contaminate +the yeast ferments.</p> + +<p id="p-357"><b>357. Microscopic examination.</b>—Place a drop of the +cultural liquid on a slide and examine under the highest +power of the microscope. What do you see? These egg-shaped +bodies are yeast plants, unicellular organisms like +the pleurococcus. Do you see any chlorophyll? Are the +yeasts parasitic? How do you know? What do they live +on? (Suggestion: What food substance that has disappeared +was put into the culture liquid?) In getting their nourishment +from the sugar, these fungi disintegrate it into alcohol +and carbon dioxide, which is a process of fermentation. It<span class="pagenum" id="Page_316">[Pg 316]</span> +is the bubbles of gas that were seen rising in the liquid which +cause beer to effervesce and bread to rise. They permeate +the dough and by their expansion produce the sponginess +peculiar to leavened bread. Look for a cell with a bud forming +on it; from what part does it appear to grow? Where a +number of buds remain for some time attached to the mother +cell (<a href="#i_325">Fig. 449</a>), they form a <em>colony</em>. Make a sketch of a +single cell and of a colony of two or more adherent ones, +labeling all the parts. If the cell wall cannot be made out +clearly, run a little glycerine, or salt water, under the cover +glass with a medicine dropper. What causes the contents of +the cell to contract and leave the wall? (<a href="#p-56">56</a>, <a href="#p-59">59</a>.)</p> + +<p id="p-358"><b>358. Reproduction.</b>—From time to time buds break away +from the mother cell and form new individuals or colonies +of their own. This process is called multiplication by budding, +and is only another form of cell division.</p> + +<p>Whenever reproduction takes place by other means than +seeds or spores, it is said to be <em>vegetative</em>. This sort of reproduction +is not confined to unicellular plants, but exists also +among the phanerogams, the propagation of species by means +of buds, tubers, rootstocks, runners, grafting, and the like +being variations of the same process. On the other hand, +yeasts and bacteria and the unicellular algæ have the power, +under extreme conditions, to form resting spores, which +sometimes lie dormant for years and resume their activity +when favorable conditions return.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. When is fermentation useful to man?</p> + +<p>2. What is the effect on canned fruits and vegetables if yeast cells get +into them?</p> + +<p>3. Why does milk turn sour in warm weather? (<a href="#p-350">350</a>, <a href="#p-351">351</a>; <a href="#exp-96">Exp. 96</a>.)</p> + +<p>4. Why do buttermilk and clabber spoil if left standing too long? +(<a href="#p-345">345</a>, <a href="#p-356">356</a>.)</p> + +<p>5. What causes bread to be “heavy”? (<a href="#p-356">356</a>, <a href="#p-357">357</a>.)</p> + +<p>6. Why will dough not rise unless kept in a warm place? (<a href="#exp-96">Exp. 96</a>.)</p> + +<p>7. Why is beer kept cold during fermentation? (<a href="#p-350">350</a>, <a href="#p-356">356</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_317">[Pg 317]</span></p> + + +<h4 id="CH_X_III_C">C. <span class="smcap">Rusts</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—A leaf of wheat affected with red rust; a leaf or a stalk +with black rust. Some barberry leaves with yellowish pustules on the +under side, which under the lens look like clusters of minute white corollas. +These are popularly known as “cluster cups.” As the spots on barberry +occur in spring, the red rust in summer, and the black rust in autumn, +gather the specimens as they can be found, and preserve for use.</p> + +<figure class="figright illowp25" id="i_327" style="max-width: 20em;"> + <img class="w100" src="images/i_327.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 450, 451.</span>—Leaf +of wheat affected +with orange +leaf-rust (<i>Puccinia +rubigo-vera</i>), uredo +stage: 450, upper +side of leaf; 451, +under side.</p></figcaption> +</figure> + +<p>The orange leaf, or brown, rust (<i>Puccinia rubigo-vera</i>) is more common +in some parts of the country than the ordinary wheat rust (<i>Puccinia +graminis</i>), but the two are so much alike that the directions given will +do for either. If the orange leaf-rust (so named from its color, and not +from any connection with orange leaves, the logical relation of the words +being orange leaf-rust, and not orange-leaf rust) is used, the cups and +pustules should be looked for on plants of the borage family—comfrey, +hound’s-tongue, etc. The orange leaf-rust of apple is caused by a fungus +which will serve to illustrate the same class of parasites. +The “teleuto” stage of this will be found on cedar +trees, in the excrescences commonly known as “cedar +apples”; the “cluster cups” on the leaves of apple +and haw trees affected with the disease.</p> +</div> + +<p id="p-359"><b>359. Red rust.</b>—Uredo stage. Examine +a leaf of “red rusted” wheat under the lens, +and notice the little oblong brown dots that +cover it. These are clusters of spore cases, +and are the only part that appears above the +surface. Viewed under the microscope, the +red rust will be seen to consist of a mycelium +(see <a href="#i_328">Fig. 452</a>), which ramifies through the +tissues of the leaf and bears clusters of single-celled +reddish spores that break through the +epidermis and form the reddish brown spots +and streaks from which the disease takes its +name. These spores, falling upon other +leaves, germinate in a few hours and form +new mycelia, from which, in six to ten days, +fresh spores arise. Formerly this was thought to complete the +life history of the fungus, to which the name of <em>Uredo</em> was +given. It is now known, however, that the red rust is merely a<span class="pagenum" id="Page_318">[Pg 318]</span> +stage in the life cycle of the plant, and to this stage the old +name uredo is applied, the spores being called <em>uredospores</em>.</p> + +<p id="p-360"><b>360. Black rust.</b>—Teleuto stage. Next examine with a +lens a part of the plant attacked by black rust. Do you +observe any +difference except +in the +color? Do the +two kinds of +rust attack all +parts of the +plant equally? +If not, what +part does each +seem to affect more particularly? At what season does the +black rust appear most abundantly? Place a section of the +diseased part under the microscope and notice that the difference +in color is due to a preponderance of long, two-celled +bodies with very thick, black walls (<a href="#i_328a">Fig. 453</a>). These +are called <em>teleutospores</em>, +a word +meaning “final +spores,” because +they are +formed only +toward the end +of the season. +They are developed +from +the same mycelium +with the +uredospores, +and are not a +product of the latter, but collateral with them and belong to +the same stage in the life history of the fungus. After they +appear, the uredospores cease to be developed at all, and<span class="pagenum" id="Page_319">[Pg 319]</span> +only the dark teleutospores are produced. These remain on +the culms in the stubble fields over winter, ready to begin +the work of reproduction in spring. For this reason the +teleutos are popularly known as “winter spores” in contradistinction +to the uredos, or “summer spores,” whose activity +is confined to the warm months.</p> + +<figure class="figcenter illowp70" id="i_328" style="max-width: 50em;"> + <img class="w100" src="images/i_328.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 452.</span>—Uredo spores of wheat rust (<i>Puccinia graminis</i>), +magnified. (<i>From</i> <span class="smcap">Coulter’s</span> “Plant Structures.”)</p></figcaption> +</figure> + +<figure class="figcenter illowp70" id="i_328a" style="max-width: 50em;"> + <img class="w100" src="images/i_328a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 453.</span>—Teleutospores of wheat rust, magnified. +(<i>From</i> <span class="smcap">Coulter’s</span> “Plant Structures.”)</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_329" style="max-width: 20em;"> + <img class="w100" src="images/i_329.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 454.</span>—Teleutospore +germinating +and forming sporidia, +<i>s</i>, <i>s</i>. (<i>From</i> <span class="smcap">Coulter’s</span> +“Plant Structures.”)</p></figcaption> +</figure> + +<p>It was formerly supposed that black rust was caused by a +different fungus from that producing red rust, and to it the +name <em>Puccinia</em> was given. This has been +retained as a general designation for all fungi +undergoing these two phases, and the particular +form of fungus that we are now considering +is known in all its stages as <i>Puccinia +graminis</i>.</p> + +<p id="p-361"><b>361. The nonparasitic stage.</b>—The formation +of teleutospores completes that portion +of the life history of the fungus during +which it is parasitic on wheat and grasses of +different kinds. In spring they begin to +germinate on the ground, each cell producing +a small filament, from which arise in turn +several small branches. Upon the tip of +each of these branches is developed a tiny +sporelike body called a <em>sporidium</em> (<a href="#i_329">Fig. 454</a>), +which continues the generation of the rust +fungus through the next stage of its existence. +The filament which bears these sporidia is not parasitic, +but when the sporidia ripen and the spores contained +in them are scattered by the wind, there begins a second +parasitic phase, which forms the most curious part of this +strange life history.</p> + +<p id="p-362"><b>362. The æcidium.</b>—Examine next the under side of +some barberry leaves (or comfrey, etc., if orange leaf-rust +is used) for clusters of small whitish bodies that appear +under the lens like little white corollas with yellow anthers +in the center. Examine a section of one of these under the<span class="pagenum" id="Page_320">[Pg 320]</span> +microscope and notice that the yellow substance is composed +of regular layers of colored spores. The corolla-like +receptacles containing them, popularly known as “cluster +cups,” are borne on a mycelium produced from the +spores described in the last paragraph. This mycelium is +parasitic on barberry or other leaves, according to the kind +of fungus, and was long believed to be a distinct plant, to +which the name <i>Æcidium</i> +(pl., <i>Æcidia</i>) was +given. This term is +now applied to the +cluster cups, and those +fungi which at any +period of their life history +produce them are +called æcidium fungi.</p> + +<figure class="figright illowp50" id="i_330" style="max-width: 50em;"> + <img class="w100" src="images/i_330.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 455.</span>—Section through a barberry leaf, +showing on the upper side two spermogonia, <i>s</i>, <i>s</i>; +and on the under side, an æcidium, <i>æ</i>.</p></figcaption> +</figure> + +<p id="p-363"><b>363. Spermogonia.</b>—On +the upper surface +of the leaves that +bear the æcidia, notice +some small black dots +hardly larger than pin +points, but which, +when sufficiently magnified, +appear as little +flask-shaped bodies (<a href="#i_330">Fig. 455</a>) under the epidermis. These are +known as <em>spermogonia</em>, or <em>pycnidia</em>. When mature, they +break through the epidermis so that the necks protrude, and +discharge a quantity of minute cells or spores, very like some +that, later on, we shall find playing an important part in the +reproductive processes of certain other fungi, and of mosses +and liverworts. In the rust fungi, however, their function is +not understood. They may possibly be survivals of organs +which were once active in the life processes of the plant, but +have become useless under changed conditions. Do such +organs throw any light on the evolutionary history of plants?</p> + +<p><span class="pagenum" id="Page_321">[Pg 321]</span></p> + +<figure class="figright illowp60" id="i_331" style="max-width: 63em;"> + <img class="w100" src="images/i_331.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 456.</span>—A species of “cedar apple” (<i>Gymnosporangum</i>), +showing the uredo-teleuto stage of +the apple rust fungus. (<i>From</i> a photograph by +Prof. F. E. Lloyd.)</p></figcaption> +</figure> + +<p id="p-364"><b>364. Connection between barberry and wheat rust.</b>—With +the discharge of the æcidium spores, the part of the +life cycle of the fungus spent on the barberry comes to an +end, and it is ready to begin the uredo-teleuto stage over +again as soon as it finds a suitable host. Where there are no +barberries, it is capable of propagating without them, either +by adapting itself to some other host plant, or by omitting +the æcidium stage altogether. +The parasitic +habit being an +acquired one, the +fungus, like some animal +organisms that +we know of, can often +be “educated” by +force of circumstances +into tolerating, +and even thriving +upon, foods which +under other circumstances +it would reject. +The wheat rust +is known to be capable +of propagating +year after year in the +uredo stage, the +spores surviving +through the winter on volunteer grains and grasses; and in +no other country in the world does rust do greater damage +to the wheat crop than in Australia, where the barberry +is practically unknown. This power of accommodation +possessed by many parasites is one of the difficulties the +agriculturist has to contend with in the development of rustproof +varieties.</p> + +<p id="p-365"><b>365. Polymorphism.</b>—Plants that pass through different +stages in their life history are said to be <em>polymorphic</em>, that<span class="pagenum" id="Page_322">[Pg 322]</span> +is, of many forms. The habit is very common among the +lower forms of vegetation. The fact that one or more of +the phases are sometimes omitted, as the æcidium phase +of wheat rust in warm climates, suggests the idea that it +may be of use in helping the plant to tide over difficult +conditions. Besides giving better chances of obtaining +nourishment, it probably has the same effect as cross fertilization +among flowering plants, in imparting increased +strength and vitality to the succeeding generation. Wheat +rust produced from barberry æcidia is said to be much more +vigorous—and consequently more destructive—than when +derived from a uredo that has reproduced itself for several +generations.</p> + +<p id="p-366"><b>366. The damage done by rust</b> to the host is through the +destruction of its tissues by the mycelium. The chlorophyll +is destroyed so that the plant can no longer manufacture +food, and is too starved to produce good grain. There are +many varieties of wheat rust, which have been found on +twenty-seven different kinds of grain. Most of them are +specialized to a particular host plant and will not, ordinarily +<a href="#p-364">(364)</a>, infest any other. Has this fact any bearing upon the +production of rustproof varieties?</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Is a farmer wise to leave scabby and mildewed weeds and bushes +in the neighborhood of his grain fields? (<a href="#p-364">364</a>, <a href="#p-365">365</a>.)</p> + +<p>2. Are there any objections to the presence of volunteer grain stalks +along roadsides and in fence corners during winter? (<a href="#p-364">364</a>.)</p> + +<p>3. Should cedar trees be allowed to grow near an apple orchard? Give +a reason for your answer. (p. <a href="#Page_317">317</a>, Material.)</p> + +<p>4. Should diseased plants be plowed under? (<a href="#p-361">361</a>.)</p> + +<p>5. What disposition should be made of them?</p> + +<p>6. Ought diseased fruits to be left hanging on the tree?</p> + +<p>7. Why is it necessary to pick over and discard from a crate or bin all +decaying fruits and vegetables?</p> + +<p>8. Does a rotation of crops tend to prevent the spread of disease in +plants? Give reasons for your answer.</p> + +<p>9. Are rustproof varieties to be relied on indefinitely? (<a href="#p-364">364</a>.)</p> +</div> + +<p><span class="pagenum" id="Page_323">[Pg 323]</span></p> + + +<h4 id="CH_X_III_D">D. <span class="smcap">Mushrooms</span></h4> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Any kind of gilled mushroom in different stages of development, +with a portion of the substratum on which it grows, containing +some of the so-called spawn. The common mushroom sold in the +markets (<i>Agaricus campestris</i>) can usually be obtained without difficulty. +Full directions for cultivating this fungus are given in Bulletin 53 of the +U. S. Department of Agriculture. From 6 to 12 hours before the lesson +is to begin, cut the stem from the cap of a mature specimen, close up to +the gills, lay it, gills downward, on a piece of clean paper, cover with a bowl +or pan to keep the spores from being blown about by the wind, and leave +until a print (<a href="#i_337">Fig. 466</a>) has been formed.</p> +</div> + +<p id="p-367"><b>367. Mushrooms and toadstools.</b>—The popular distinction +which limits the term “mushroom” to a single species, +the <i>Agaricus campestris</i>, and classes all others as toadstools, +has no sanction in botany. All mushrooms are toadstools +and all toadstools are mushrooms, whether poisonous or +edible. The real distinction is between mushrooms and +puffballs, the former term being more properly applied to +fungi which have the spore-bearing surface exposed.</p> + +<p id="p-368"><b>368. Examination of a typical specimen.</b>—The most +highly specialized of the fungi, and the easiest to observe on +account of their size and abundance, are the mushrooms +that are such familiar objects after every summer shower. +The <em>gilled</em> kind—those with the rayed laminæ under the +cap—are usually the most easily obtained. Specimens +should be examined as soon after gathering as possible, since +they decay very quickly.</p> + +<p id="p-369"><b>369. The mycelium.</b>—Examine some of the white fibrous +substance usually called spawn through a lens. Notice +that it is made up of fine white threads interlacing with each +other, and often forming webby mats that ramify to a considerable +distance through the substratum of rotten wood +or other material upon which the fungus grows. This webby +structure, often mistaken for root fibers, is the thallus or +true vegetative body of the plant, the part rising above +ground, and usually regarded as the mushroom, being only +the fruit, or reproductive organ. Place some of the mycelium<span class="pagenum" id="Page_324">[Pg 324]</span> +under the microscope and notice that it is +composed of delicate filaments made up of +single cells placed end to end, as in Spirogyra +<a href="#p-341">(341)</a>. These filaments are called +<em>hyphæ</em>.</p> + +<p id="p-370"><b>370. The button.</b>—Look on the mycelium +for one of the small round bodies +called buttons (<a href="#i_334">Fig. 457</a>). These are the +beginning of the fruiting body popularly +known as the mushroom, and are of various +sizes, some of the youngest being +barely visible to the naked eye. After a +time they begin to elongate and make +their way out of the substratum.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp90" id="i_334" style="max-width: 30em;"> + <img class="w100" src="images/i_334.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 457.</span>—Mycelium +of a mushroom (<i>Agaricus +campestris</i>), with young +buttons (fruiting organs) +in different stages: 1, 2, +3, 4, 5, sections of fructification +at successive periods +of development; <i>m</i>, +mycelium; <i>st</i>, stipe; <i>p</i>, +pileus; <i>l</i>, gill, or lamina; +<i>v</i>, veil.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp90" id="i_334a" style="max-width: 30em;"> + <img class="w100" src="images/i_334a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 458.</span>—Diagram of unexpanded +<i>Amanita</i>, showing parts: <i>a</i>, +volva; <i>b</i>, pileus; <i>c</i>, gills; <i>d</i>, veil; <i>e</i>, +stipe; <i>m</i>, mycelium.</p></figcaption> +</figure></td></tr></table> + +<p id="p-371"><b>371. The veil and the volva.</b>—Make a +vertical section through the center of one +of the larger buttons after it is well above +ground, and sketch. Notice whether it is +entirely enveloped from root to cap in a covering membrane—the +<em>volva</em> (<a href="#i_334a">Fig. 458</a>, <i>a</i>)—or +whether the enveloping membrane +extends only from the +upper part of the stem to the +margin of the cap—the <em>veil</em> (<a href="#i_334a">Fig. +458</a>, <i>d</i>); whether it has both veil +and volva, or finally, whether it +is naked, that is, devoid of both.</p> + +<p id="p-372"><b>372. The stipe, or stalk.</b>—Notice +this as to length, thickness, +color, and position; that is, +whether it is inserted in the +center of the cap or to one side +(excentric), or on one edge (lateral). +Observe the base, whether +bulbous, tapering, or straight, +and whether surrounded by a<span class="pagenum" id="Page_325">[Pg 325]</span> +cup, or merely by concentric rings or ragged +bits of membrane (the remains of the +volva). Look for the <em>annulus</em> or ring (remains +of the veil) near the insertion of the +stipe into the cap, and if there is one, notice +whether it adheres to the stipe, or moves +freely up and down (<a href="#i_335">Fig. 459</a>, <i>a</i>); whether +it is thick and firm, or broad and membranous +so that it hangs like a sort of curtain +round the upper part of the stipe (<a href="#i_337a">Fig. +467</a>, <i>a</i>). Break the stem and notice whether +it is hollow or solid; observe also the texture, +whether brittle, cartilaginous, fibrous, or +fleshy.</p> + +<table class='autotable'> +<tr><td class='wd50'> +<figure class="figcenter illowp70" id="i_335" style="max-width: 13.25em;"> + <img class="w100" src="images/i_335.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 459.</span>—Parasol +mushroom (<i>Lepiota +procera</i>), showing +movable annulus: <i>st</i>, +stipe; <i>a</i>, annulus, or +ring; <i>u</i>, umbo; <i>p</i>, <i>p</i>, +floccose patches left +by volva.</p></figcaption> +</figure> +</td><td class='wd50'> +<figure class="figleft illowp70" id="i_335a" style="max-width: 30em;"> + <img class="w100" src="images/i_335a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 460.</span>—Chanterelle +(<i>Cantharellus cibarius</i>), with +infundibuliform pileus and +decurrent gills.</p></figcaption> +</figure></td></tr></table> + +<p id="p-373"><b>373. The pileus, or cap.</b>—Observe this as +to color and surface, whether dry, or moist +and sticky; smooth, or covered with scurf +or scales left by the remains of the volva, as it was stretched +and broken up by the expanding cap (<a href="#i_335">Fig. 459</a>, <i>p</i>, <i>p</i>). Note +also the size and shape, whether conical, +expanded, funnel-shaped (<a href="#i_335a">Fig. 460</a>), +or <em>umbonate</em>—having a protuberance +at the apex (<a href="#i_335">Fig. 459</a>)—or whether the +margin is turned up at the edge (revolute, +<a href="#i_337a">Fig. 467</a>), or under (involute, <a href="#i_335">Fig. 459</a>).</p> + +<p id="p-374"><b>374. The gills, or laminæ.</b>—Look at +the under surface and notice whether +the gills are broad or narrow, whether +they extend straight from stem to margin, +or are rounded at the ends, or +curved, toothed, or lobed in any way. +Notice their attachment to the stipe, +whether <em>free</em>, not touching it at all; <em>adnate</em>, attached squarely +to the stem at their anterior ends; or <em>decurrent</em>, running +down on the stem for a greater or less distance (<a href="#i_335a">Fig. 460</a>).</p> + +<p><span class="pagenum" id="Page_326">[Pg 326]</span></p> + +<table class='autotable'> +<tr><td class='wd40'> +<figure class="figcenter illowp100" id="i_336" style="max-width: 30em;"> + <img class="w100" src="images/i_336.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 461-463.</span>—Section of a +gilled mushroom: 461, through +one side, showing sections of the +pendent gills, <i>g</i>, <i>g</i> (slightly magnified); +462, one of the gills +more enlarged, showing the central +tissue of the trama, <i>tr</i>, and +the broad border formed by the +hymenium, <i>h</i>; 463, a small section +of one side of a gill very +much enlarged, showing the +club-shaped basidia, <i>b</i>, <i>b</i>, standing +at right angles to the surface, +bearing each two small branches +with a spore, <i>s</i>, <i>s</i>, at the end. +The sterile paraphyses, <i>p</i>, are +seen mixed with the basidia.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp100" id="i_336a" style="max-width: 30em;"> + <img class="w100" src="images/i_336a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 464, 465.</span>—A tube fungus (<i>Boletus edulis</i>): +464, entire; 465, section, showing position of the +tubes.</p></figcaption> +</figure></td></tr></table> + +<p id="p-375"><b>375. The hymenium.</b>—Cut a tangential section through +one side of the pileus and sketch the section of the gills as +they appear under a lens, or a low +power of the microscope. Notice +that the blade consists of a central +portion called the <em>trama</em> (<i>tr</i>, <a href="#i_336">Fig. 462</a>) +and a somewhat thickened portion, +<i>h</i>, constituting the <em>hymenium</em>, or +spore-bearing surface. Now examine, +under a high power, a small section +from the edge of a gill, including +a bit of the trama. Notice that this +last consists of a tissue of mycelial +cells (<a href="#i_336">Fig. 463</a>) covered by the hymenium, +or spore-bearing membrane, +which is thickly clothed with a layer +of elongated, club-shaped cells (<i>b</i>, <i>b</i> +and <i>p</i>, <i>p</i>, <a href="#i_336">Fig. 463</a>) set upon it at right +angles to the surface. Some of these +put out from two to four, or in some +species as many as eight, little +prongs, each bearing a spore (<i>s</i>, <i>s</i>, <a href="#i_336">Fig. +463</a>), while others remain +sterile. The spore-bearing +cells are called +<em>basidia</em>; the sterile +ones, <em>paraphyses</em>; and +the whole spore-bearing surface together, the <em>hymenium</em>, from +a Greek word meaning a membrane. It is from the presence<span class="pagenum" id="Page_327">[Pg 327]</span> +of this expanded fruiting membrane that the class of mushrooms +we are considering gets its botanical name, <i>Hymenomycetes</i>, +membrane fungi. The hymenium is not always +borne on gills, but is arranged in various ways which serve +as a convenient basis for distinguishing the different orders. +In the tube fungi, to which the edible +boletus belongs (<a href="#i_336a">Figs. 464, 465</a>), the +basidia are placed along the inside of +little tubes that line the under side +of the pileus, giving it the appearance +of a honeycomb. In another +order, the porcupine fungi, they are +arranged on the outside of projecting +spines or teeth, while in the +morelles they are held in little cups +or basins.</p> + +<table class='autotable'> +<tr><td class='wd50'> +<figure class="figcenter illowp80" id="i_337" style="max-width: 30em;"> + <img class="w100" src="images/i_337.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 466.</span>—Spore print of a +gilled mushroom.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp80" id="i_337a" style="max-width: 30em;"> + <img class="w100" src="images/i_337a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 467.</span>—Deadly agaric +(<i>Amanita phalloides</i>), showing +the broad pendent annulus, +<i>a</i>, formed by the ruptured +veil; the cup at the +base, <i>c</i>, and floccose patches +on the pileus, left by the +breaking up of the volva.</p></figcaption> +</figure></td></tr></table> + +<p id="p-376"><b>376. Spore prints.</b>—When the +gills are ripe, they shed their spores in great abundance. +Take up the pileus that was laid on paper, as directed under +Material, on <a href="#Page_323">page 323</a>, and examine +the print made by the discharged +spores; it will be found to give an +exact representation of the under side +of the pileus.</p> + +<p id="p-377"><b>377. The spores.</b>—Notice the color +of the spores as shown in the print. +This is a matter of importance in distinguishing +gill-bearing fungi, which are +divided into five sections according to +the color of the spores. One source of +danger, at least, to mushroom eaters +would be avoided if this difference was +always attended to, for the deadly +amanita (<i>Amanita phalloides</i>) and the +almost equally dangerous fly mushroom +(<i>A. muscaria</i>) both have white spores,<span class="pagenum" id="Page_328">[Pg 328]</span> +while the favorite edible kind (<i>Agaricus campestris</i>), though +white-gilled when young, produces dark, purple-brown spores +that cannot fail to distinguish it clearly for any one who will +take the trouble to make a print.</p> + +<p id="p-378"><b>378. Economic properties.</b>—Most of the wood-destroying +fungi belong to this and allied orders. They are among +the worst enemies the forester has to deal with <a href="#p-140">(140)</a>, and +millions of feet of +lumber are destroyed +every year by them.</p> + +<figure class="figright illowp60" id="i_338" style="max-width: 50em;"> + <img class="w100" src="images/i_338.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 468.</span>—Portion of the root of a maple affected +with rot caused by the mycelium of a fungus that +has penetrated to its interior.</p></figcaption> +</figure> + +<p>Over seven hundred +kinds of fungi +growing in the United +States have been described +as edible, but +the evil repute into +which the whole class +has been brought by +the poisonous qualities +of a few species, +and the difficulty, to +any but an expert, of +distinguishing between +these and the harmless kinds, has caused them to be +generally neglected as articles of diet. While they are +pleasant relishes and furnish an agreeable variety to our daily +fare, their food value has been greatly exaggerated. They +contain a large proportion of water, often over 90 per cent, +and the most valued of them, the <i>Agaricus campestris</i>, is +about equivalent to cabbage in nutrient properties.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Why are mushrooms generally grown in cellars? (<a href="#p-186">186</a>, <a href="#p-343">343</a>.)</p> + +<p>2. Name any fungi you know of that are good for food or medicine or +any other purpose.</p> + +<p>3. Name the most dangerous ones you know of.</p> + +<p><span class="pagenum" id="Page_329">[Pg 329]</span></p> + +<p>4. Do you find fungi most abundant on young and healthy trees, or +on old, decrepit ones? Account for the difference. (<a href="#p-141">141</a>, <a href="#p-343">343</a>, <a href="#p-378">378</a>.)</p> + +<p>5. Do you ever find them growing on perfectly sound wood anywhere?</p> + +<p>6. Are they ever beneficial to a tree? (<a href="#p-86">86</a>.)</p> + +<p>7. Is it wise to leave old, unhealthy trees and decaying trunks in a +timber lot?</p> +</div> + + +<h3 id="CH_X_IV">IV. LICHENS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Specimens can be found almost everywhere, growing +on rocks, walls, logs, stumps, and trees. Some of the more common kind +are: <i>Parmelia</i>, recognizable by the shallow spore cups borne on the upper +surface of the thallus; <i>Cladonia</i>, by the little stalked receptacles, like +goblets, in which its spores are held; <i>Physcia</i>, by its bright orange color. +Where practicable, it is well to have several different kinds for comparison. +Iceland moss (<i>Cetraria islandica</i>) can generally be obtained from the +grocers, and is a good example of an intermediate form between foliaceous +and fruticose lichens.</p> + +<p>If the specimens are very dry, they will be too brittle to handle conveniently, +and should be moistened by soaking a short time in water. This +will render them quite flexible and also bring out the green color more +clearly.</p> +</div> + +<figure class="figcenter illowp100" id="i_339" style="max-width: 50em;"> + <img class="w100" src="images/i_339.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 469.</span>—Foliaceous lichens: <i>A</i>, <i>Xanthoria (Physcia) parietina</i>; <i>B</i>, <i>Parmelia +conspersa</i>; <i>a</i>, spore cups.</p></figcaption> +</figure> + +<p id="p-379"><b>379. Examination of a typical specimen.</b>—The commonest +kind of lichens, and generally the most easily obtained, +are those that grow on rocks and tree trunks in flat, +spreading patches. Their margins are much dented and<span class="pagenum" id="Page_330">[Pg 330]</span> +curled, giving them a somewhat leaflike appearance, whence +they are called “foliaceous” lichens. This broad, expanded +body is the thallus, or vegetative part, as distinguished from +its reproductive part. Examine carefully the thallus of +your specimen. Note the size and shape of the indentations. +Is there any order or regularity about them, such as was +observed in the lobing of leaves? Is there any difference +in color between the upper and under sides? What other +differences do you notice? Do you see anything like hairs, +or rootlets, on the under side? Mount one of them in water +and place under the microscope. What does it look like? +Compare with one of the hairs from a leaf of mullein, gromwell, +blueweed, or other hairy plant, with the hypha of a +fungus mycelium, and with your study of the root hair in +<a href="#p-67">67</a> (<i>a</i>). Is it a hair or a root? These rootlike hairs are +called <em>rhizoids</em>, and serve to anchor the lichen to its substratum. +Look on the upper side for little cup-shaped or +saucer-shaped receptacles. On what part of the thallus +are they situated? Examine +with a lens and see +if you can make out what +they contain. These cups +are the spore cases. The +lichen fungus belongs to +the division of sac fungi, +which produce their +spores in closed sacs, or +cups.</p> + +<figure class="figright illowp55" id="i_340" style="max-width: 40em;"> + <img class="w100" src="images/i_340.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 470.</span>—Portion of the thallus of a lichen, +magnified, showing imprisoned algæ.</p></figcaption> +</figure> + +<p id="p-380"><b>380. Structure of the +thallus.</b>—Make a thin +section through a thallus and place under the microscope. +Notice the small green bodies enveloped in the hyphæ of the +fungus. Are they most abundant near the upper or the lower +epidermis? Has their green color anything to do with this, +and with the difference in color between the two surfaces of +the thallus? (<a href="#p-184">184</a>.) Do they look like chlorophyll granules?<span class="pagenum" id="Page_331">[Pg 331]</span> +Can you tell what they are? Compare with your study of +the unicellular algæ <a href="#p-337">(337)</a> and with <a href="#i_310">Fig. 429</a>. Does this +throw any light on their real nature?</p> + +<figure class="figcenter illowp80" id="i_341" style="max-width: 50em;"> + <img class="w100" src="images/i_341.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 471.</span>—Artificial lichen mycelium, <i>m</i>, made by sowing spores of a fungus, +<i>sp</i>, among alga cells, <i>a</i>.</p></figcaption> +</figure> + +<p id="p-381"><b>381. The lichen thallus a composite body.</b>—You will +probably have no difficulty in making out that these small +round bodies are green algæ of some kind, but of what species +will depend upon the kind of lichen with which it is associated. +In Cladonia and the bearded lichen (<a href="#i_343">Fig. 473</a>), it is a protococcus; +in other forms, a pleurococcus or a nostoc—and so +on, each species of lichen fungus being specialized to a certain +form of alga. The great botanist, De Bary, showed +that it is even possible to produce a lichen thallus artificially +by sowing the spores of a fungus among the cells of the particular +alga with which it is able to unite. The spores will +germinate without the alga, but soon perish unless they come +in contact with the right one. It is thus made clear that the +lichen plant as a whole is a combination of elements belonging +to two distinct orders, the algæ and fungi, but so closely +associated as to constitute practically a single individual.</p> + +<p><span class="pagenum" id="Page_332">[Pg 332]</span></p> + +<p id="p-382"><b>382. Slavery, or partnership?</b>—Now, what can be the +object of this peculiar association? Is it a symbiosis, or +a case of enslavement? The fungi, as we know, are all +parasites, unable to manufacture their own food or to exist +at all except at the expense of other organisms, living or dead. +But the lichens have refined upon the gross rapacity of their +order, and instead of indiscriminately destroying the hosts +that furnish their nourishment, have used their victims to +better purpose by converting them into contented, well-fed +slaves! The imprisoned algæ perform for them the same +service that the chlorophyll bodies do for the higher plants, +and so the lichen fungi have the advantage of other parasites +in getting their food manufactured at home, so to speak. +And while the algæ have to do double work in order to feed +both themselves and their masters, the fungus, in return, +shelters them against cold and drought, and prolongs their +growing period by giving them a more continuous supply +of moisture and food materials, +which it draws from the +substratum by means of its +rhizoids. In this way both +plants are enabled to live in +situations that neither could +occupy without the other.</p> + +<figure class="figright illowp40" id="i_342" style="max-width: 30em;"> + <img class="w100" src="images/i_342.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 472.</span>—A crustaceous lichen +(<i>Graphis elegans</i>) growing on holly: <i>A</i>, +natural size; <i>B</i>, slightly magnified.</p></figcaption> +</figure> + +<p id="p-383"><b>383. Reproduction.</b>—The +multiplication of the lichen +algæ is exclusively vegetative. +The fungus, on the other +hand, reproduces normally +by spores, and the fruiting +bodies found on the thallus +originate from the fungus +mycelium.</p> + +<p id="p-384"><b>384. Classification.</b>—To +be strictly accurate, the +two kinds of vegetable bodies<span class="pagenum" id="Page_333">[Pg 333]</span> +that make up the lichen thallus would probably have to be +classified separately, as algæ or fungi, respectively, but as +fructification is the generally accepted basis of classification, +and the plant body is too intimately permeated with both +kinds of tissue to be divided, each lichen body as a whole is +classed with its particular kind of fungus. The entire group, +on account of the distinctive characters that mark it, is +placed in a separate order of its own. This includes three +principal divisions, distributed according to the shape of the +thallus, and its habit of growth: (1) <em>Crustaceous</em>, those that +adhere closely to the substratum, as if glued or inscribed on +it; (2) <em>Foliaceous</em>, with a broad, more or less lobed and leaflike +thallus that adheres loosely to the substratum by means +of rhizoids springing from its under surface; (3) <em>Fruticose</em>, +with branching, stemlike thallus attached at the base like a +regularly rooting plant (<a href="#i_343">Figs. 473, 474</a>). Among these are +the Iceland moss, used as an article of food by man, and the +reindeer moss (<i>Cladonia rangiferina</i>), which is the chief sustenance +of the reindeer.</p> + +<figure class="figcenter illowp100" id="i_343" style="max-width: 50em;"> + <img class="w100" src="images/i_343.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 473, 474.</span>—Fruticose lichens: 473, <i>Usnea barbata</i>, bearded lichen; 474, +<i>Cladonia rangiferina</i>, reindeer moss: <i>A</i>, sterile; <i>B</i>, fruiting portion.</p></figcaption> +</figure> + +<p><span class="pagenum" id="Page_334">[Pg 334]</span></p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Have lichens any economic value? (<a href="#p-384">384</a>.)</p> + +<p>2. In what way are they most useful? (<a href="#p-320">320</a>.)</p> + +<p>3. Do you find them, as a general thing, on healthy young trees and +boughs, or on old ones, and those showing signs of decay?</p> + +<p>4. Do you ever find them growing on trees or other objects in densely +inhabited areas,—cities, large towns, and manufacturing centers?</p> + +<p>5. Do they grow more thickly on the shady (northern) side of rocks, +walls, and trees growing in the open, than on the sunny and (presumably) +warmer sides?</p> + +<p>6. Mention some ways in which a growth of lichens might be beneficial +to a tree.</p> + +<p>7. In what ways could it be harmful?</p> +</div> + + +<h3 id="CH_X_V">V. LIVERWORTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Liverworts can generally be found growing with mosses +in damp, shady places, and are easily recognized by their flat, spreading +habit, which gives them the appearance of green lichens. <i>Marchantia +polymorpha</i> (<a href="#i_345">Fig. 475</a>), one of the largest and best specimens for study, +is common in shady, damp ground throughout the states. It is diœcious, +and specimens bearing both male and female organs should be provided. +<i>Lunularia</i>, a smaller species that can be recognized by the little crescent-shaped +receptacles on some of the divisions of the thallus, is abundant +in greenhouses on the floor, or on the sides of pots and boxes kept in damp +places; but the spore-bearing receptacles are seldom or never present, +the species being an introduced one and possibly rendered sterile by +changed conditions. <i>Anthoceros</i> (<a href="#i_307a">Fig. 426</a>) and leafy liverworts, such +as that shown in <a href="#i_352">Fig. 484</a>, also make good examples for study.</p> + +<p id="exp-97"><span class="smcap">Experiment 97. Why are the upper and under sides of a liverwort +different?</span>—Plant a growing branch of marchantia, or of any +flat, spreading liverwort, in moist earth so that the upper side will lie next +the soil, and watch for a week or two, noting the changes that take place. +What would you infer from these as to the cause of any differences that +may have been observed between the two surfaces?</p> +</div> + +<p id="p-385"><b>385. Examination of a typical liverwort</b>—The thallus.—The +broad, flat, branching organ that forms the body of the +plant is the thallus. Examine the end of each branch; +what do you find there? Are the two forks into which the +apex of the branches divides equal or unequal? Compare +the growing end with the distal one; does it proceed from<span class="pagenum" id="Page_335">[Pg 335]</span> +a true root? Notice that as the lower end dies, the growing +branches go on increasing and reproducing the thallus.</p> + +<figure class="figcenter illowp82" id="i_345" style="max-width: 51em;"> + <img class="w100" src="images/i_345.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 475, 476.</span>—Umbrella liverwort (<i>Marchantia polymorpha</i>): 475, portion of a +female thallus about natural size, showing dichotomous branching; <i>f</i>, <i>f</i>, archegonial +or female receptacles; <i>r</i>, rhizoids; 476, portion of a male thallus bearing an antheridial +disk or receptacle, <i>d</i>, and gemmæ, <i>g</i>, <i>g</i>.</p></figcaption> +</figure> + +<figure class="figright illowp30" id="i_346" style="max-width: 20em;"> + <img class="w100" src="images/i_346.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 477.</span>—A portion +of the upper epidermis +of marchantia, magnified, +showing rhomboidal +plates with a stoma in +each.</p></figcaption> +</figure> + +<p>Do you find anything like a midrib? If so, trace it through +the branches and body of the thallus; where does it end? +Does it seem to be formed like the midrib of a leaf? Hold +a piece of the thallus up to the light and see if you can detect +any veins. Is it of the same color in all parts, and if there is +a difference, can you give a reason for it? Examine the +upper surface with a lens. Peel off a piece of the epidermis, +place it under a low power of the microscope, or between +two moistened bits of glass, and hold up to the light, keeping +the upper surface toward you; what is its appearance?<span class="pagenum" id="Page_336">[Pg 336]</span> +Observe a tiny dot near the center of the rhomboidal areas +into which the epidermis is divided and compare it with +your drawings of stomata (<a href="#p-181">181</a>, <a href="#p-183">183</a>). +What would you judge that these dots +are for? While differing in structure +from the stomata of leaves, they serve +the same purposes and may be regarded +a more rudimentary form of the same +organ.</p> + +<p id="p-386"><b>386. Rhizoids.</b>—Wash the dirt from +the under side of a thallus and examine with a lens; how +does it differ from the upper surface? Do you see anything +like roots? Place one in a drop of water under the microscope. +Compare with similar organs found on the lichen +<a href="#p-379">(379)</a>. What are they? Would rhizoids be of any use on +the upper side? stomata on the under side?</p> + +<p id="p-387"><b>387. Gemmæ.</b>—Look along the upper surface for little +saucer-shaped (in lunularia, crescent-shaped) cupules (<i>g</i>, <i>g</i>, +<a href="#i_345">Fig. 476</a>). Notice their shape and position, whether on a +midrib or near the margin. Examine the contents with +a lens and see if you can tell what they are. These little +bodies, called <em>gemmæ</em>, are of the nature of buds, by which +the plant propagates itself vegetatively somewhat as the +onion and the tiger lily do by means of bulblets. Sow some +of the gemmæ on moist sand, cover them with a tumbler +to prevent evaporation, and watch them develop the thalloid +structure.</p> + +<p id="p-388"><b>388. The fruiting receptacles.</b>—Procure, if possible, +thalli with upright pedicels bearing flattened enlargements +at the top (<a href="#i_345">Figs. 475, 476</a>). These are thallus branches +modified into receptacles containing the reproductive organs, +which, in marchantia, are diœcious, the two kinds growing +on separate thalli. Notice their difference in shape, one +kind being slightly lobed or scalloped, the other rayed like +the spokes of a wheel. The first kind are known as <em>antheridial</em>, +or male, receptacles; the second as <em>archegonial</em>, or female.</p> + +<p><span class="pagenum" id="Page_337">[Pg 337]</span></p> + +<p id="p-389"><b>389. The antheridia.</b>—Examine one of the male receptacles +on both surfaces and in vertical section. Notice the +tiny egg-shaped bodies sunk in little +cavities between the lobes just under +the upper epidermis (<a href="#i_347">Fig. 478</a>). These +are antheridia. When mature, they +rupture at the apex, and multitudes of +extremely small bodies, called <em>antherozoids</em>, +or <em>spermatozoids</em>, are discharged +from them.</p> + +<table class='autotable'> +<tr><td> +<figure class="figcenter illowp75" id="i_347" style="max-width: 30em;"> + <img class="w100" src="images/i_347.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 478.</span>—Longitudinal +section of a male receptacle +of marchantia polymorpha, +magnified: <i>a</i>, antheridia; +<i>t</i>, thallus; <i>s</i>, ventral scales; +<i>r</i>, rhizoids.</p></figcaption> +</figure> +</td><td> +<figure class="figcenter illowp75" id="i_347a" style="max-width: 30em;"> + <img class="w100" src="images/i_347a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 479.</span>—Under side of an +archegonial receptacle enlarged. +The archegonia are borne +among the hairs on the under +surface, which is presented to +view in the figure; <i>f</i>, a spore +case.</p></figcaption> +</figure></td></tr></table> + +<p id="p-390"><b>390. Archegonia.</b>—Next examine one +of the female receptacles. Look on the +under surface, between the narrow divisions +of the receptacle, for radiating rows +of flask-shaped bodies with their necks +turned downward, and all surrounded +by a toothed sheath or involucre (<a href="#i_347a">Fig. +479</a>). These bodies are the archegonia, +or female organs, and correspond, loosely speaking, to the +ovaries of flowering plants. If the receptacle is a mature +one, the archegonia will be replaced +by the ripe spore cases (<em>sporangia</em>), +as at <i>f</i>, <a href="#i_347a">Fig. 479</a>.</p> + +<p>Make enlarged drawings of the +upper surface of a male and a female +receptacle, and of a vertical section +of each, passing through an antheridium +in the male, and an archegonial +row in the female receptacle. +Label the parts observed in each.</p> + +<p id="p-391"><b>391. Minute study of an archegonium.</b>—Place +under the microscope +a very thin, longitudinal section +through a ray of a receptacle containing +a young archegonium, and observe that the latter +consists of a lower portion, the <em>venter</em>, <i>v</i>, <a href="#i_348">Fig. 480</a>, and an<span class="pagenum" id="Page_338">[Pg 338]</span> +upper part, the neck, which is perforated by the <em>neck canal</em>, +<i>ca</i>. The venter contains the <em>egg cell</em>, <i>o</i>, and the ventral canal +cell, <i>vc</i>. The neck canal is filled with small cells which, +at maturity, dissolve into a mucilaginous substance that +swells on being wet and discharges itself through the top +of the neck, leaving an open passage to the venter, where +the egg cell is ready to be fertilized.</p> + +<figure class="figright illowp40" id="i_348" style="max-width: 30em;"> + <img class="w100" src="images/i_348.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 480, 481.</span>—480, young +archegonium of M. polymorpha; +<i>v</i>, ventral portion; <i>o</i>, egg +cell; <i>vc</i>, ventral canal and cells; +<i>ca</i>, neck canal with cells; 481, +the same ready for fertilization +after discharge of the mucilaginous +fluid.</p></figcaption> +</figure> + +<p>Make a drawing of the section as +seen under the microscope, labeling +all the parts.</p> + +<p id="p-392"><b>392. Fertilization.</b>—In the liverworts, +and in cryptogams generally, +this process has to take place under +water, as the antherozoids are motile +only in a liquid, but the amount required +is so small that a few drops +of rain or dew will enable them to +make their journey to the archegonium. +The mucilaginous substances +discharged from the neck canal attract +them to the mouth of the opening, +one or more of them penetrates +to the egg cell, and fertilization is accomplished. +Do you see any analogies +between this and the same +function among flowering plants? +(<a href="#p-250">250</a>, <a href="#p-251">251</a>.)</p> + +<p id="p-393"><b>393. The spore case.</b>—After fertilization the egg becomes +an <em>oöspore</em>, capable of producing a new plant. Instead, +however, of separating from the mother plant and giving +rise to an independent growth, it germinates within the archegonium +and produces there a small, stalked body, called +a <em>sporogonium</em>, or <em>sporophyte</em>, which at length ripens into +a spore case, as shown at <i>f</i>, <a href="#i_347a">Fig. 479</a>. At maturity this +capsule-like sporophyte ruptures at the apex, and discharges<span class="pagenum" id="Page_339">[Pg 339]</span> +a mass of spores, mingled with elongated filaments called +<em>elators</em>, which, by their elastic movements, assist in disseminating +the spores. These latter, on germinating, produce, +not a simple sporophyte like that which bore them, but +the thallus of the liverwort with all its complicated arrangement +of antheridia and archegonia and vegetative organs +that seem to foreshadow, by the analogies they suggest, +the coming of the higher plants.</p> + +<p id="p-394"><b>394. Sexual and asexual reproduction.</b>—We find here +a very marked change from the simple reproductive processes +observed in the algæ and fungi. In the forms thus far considered, +this function was carried on mainly by simple vegetative +fission or budding, with a more or less irregular intervention +of resting spores. If only one kind of spore is +concerned, reproduction is said to be <em>asexual</em>. When two +different kinds of cells, the egg and sperm cell, unite to form +an oöspore, as in the liverworts, reproduction is said to be +<em>sexual</em>. While sexual reproduction takes place to some +extent among both algæ and fungi, the prevailing method +among thallophytes is asexual, and may be carried on in +three different ways: by fission (and budding), by resting +spores, and by conjugation.</p> + +<p>Representing the plant body by <i>A</i> and the resting spores +by <i>a</i>, the primitive asexual processes may be expressed to +the eye by the accompanying formulas:—</p> + +<p class="noindent pad6"> +(1) Fission and budding: <i>A</i> → <i>A</i> → <i>A</i> → <i>A</i> →<br> +(2) Resting spores: <i>A a</i> → <i>A a</i> → <i>A a</i> →<br> +(3) Conjugation: <i>A</i> + <i>A</i> → <i>a</i> → <i>A</i> + <i>A</i> → <i>a</i> →</p> + +<p class="noindent">In (3), as was seen in the conjugating cells of the spirogyra +<a href="#p-342">(342)</a>, the method is a little more complicated, showing an +approach toward the sexual process. In each of these cases, +however, there is only one kind of cell concerned, while in +the liverworts there are not only different kinds, technically +known as <em>gametes</em>, but specialized organs, archegonia +and antheridia, for producing them. The thallus body +bearing these organs is termed the <em>gametophyte</em>, because it<span class="pagenum" id="Page_340">[Pg 340]</span> +bears the gametes, or sexual organs,—the suffix <em>phyte</em> meaning +a plant; for example, <em>epiphyte</em>, on or upon plants; <em>spermophyte</em>, +or <em>spermatophyte</em>, seed plant; <em>sporophyte</em>, spore plant. +The <em>sporophyte</em>, produced within the archegonium, bears +simple nonsexual spores that are capable of germinating +independently. Structurally it is a separate, individual +organism, though it does not appear as such in this class, +but lives inclosed in the archegonium, as a parasite on the +mother plant.</p> + +<p id="p-395"><b>395. Alternation of generations.</b>—If we represent the +sporophyte by <i>S</i>, the thallus, or gametophyte, by <i>G</i>, the +female gamete, or egg cell, by <i>fg</i>, the antherozoids (male +gametes) by <i>mg</i>, the fertilized egg cell, or oöspore, resulting +from their union by <i>oös</i>, and the asexual spores discharged +from the sporophyte by <i>o</i>, this complicated mode +of reproduction may be expressed diagrammatically as +follows:—</p> + +<table class="autotable fs80 alternation"> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"><i>G</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"> <i>oös</i> ⟶ <i>s</i> ⟶ <i>o</i> ⟶ <i>G</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>oös</i> ⟶ <i>s</i> ⟶ <i>o</i> ⟶ <i>G</i> ⟶ etc.</td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +</table> + +<p>A glance at the diagram will show a continual interchange +of the sexual and asexual modes of reproduction, in +which each generation gives rise to its <em>opposite</em>, the asexual +sporophyte producing the sexual gametophyte, and this in +turn, through its gametes, giving rise to the asexual sporophyte. +This regular recurrence in genealogical succession of +two differing forms is what is meant by the expression “alternation +of generations.” Analogous processes occur also +among some of the thallophytes, but as there is no well-defined +differentiation of sporophyte and gametophyte, +alternation proper may be regarded as beginning with the +bryophytes. The subject is a complicated one and somewhat +difficult to grasp, but it is important to form a correct +idea of it and to fix clearly in mind the different modes of +reproduction as we proceed from the lower to the higher forms +of vegetation, since in this way alone can their biological<span class="pagenum" id="Page_341">[Pg 341]</span> +relationships and their order of succession in the evolutionary +scale be made intelligible.</p> + + +<h3 id="CH_X_VI">VI. MOSSES</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—One of the most widely distributed of mosses is the +Sphagnum, or peat moss, so generally used by florists in packing plants for +shipment, and it can be obtained from them at almost all times. It is +rather difficult, however, to find specimens with the fruiting organs, since +they are rarely to be met with except in late autumn or early spring. +Other common forms are <i>Polytrichum</i>, <i>Funaria</i>, and <i>Mnium</i>, any of which +will meet all essential conditions of the study outlined in the text.</p> +</div> + +<figure class="figcenter illowp80" id="i_351" style="max-width: 50em;"> + <img class="w100" src="images/i_351.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 482, 483.</span>—Protonema +of a moss: 482, germinating spore; 483, protonema; +<i>kn</i>, buds; <i>r</i>, rhizoids; <i>s</i>, spore.</p></figcaption> +</figure> + +<p id="p-396"><b>396. The protonema or thallus stage.</b>—In mosses the +sexual, or gametophyte generation differs from that of +liverworts in undergoing two phases. The germinating +cells of the sporophyte do not develop immediately into +the leafy stem, which is the typical gametophyte of true +mosses, but produce first a filamentous, creeping structure +called the <em>protonema</em> (<a href="#i_351">Fig. 483</a>), that spreads over the +ground and forms the tangled green felt usually observed +where mosses are growing. Place a few of these filaments on +a slide in water, and examine under the microscope. Do +they remind you of any of the forms of algæ? Look near<span class="pagenum" id="Page_342">[Pg 342]</span> +the base of the branches for knots or enlargements, like +those seen at <i>kn</i>, <a href="#i_351">Fig. 483</a>. These are buds from which the +leafy moss stems will develop. Do they correspond to anything +observed among the thallophytes? Notice the rootlike +filaments that extend under ground; how do they differ from +the ones above ground? Why are they colorless? How +do you know that they are not true roots? [<a href="#p-67">67</a> (<i>a</i>), <a href="#p-379">379</a>.] +Sketch one of each kind of filament sufficiently enlarged to +show the cells composing it.</p> + +<p>A protonema that arises directly from the spore is said +to be <em>primary</em>, while those which sometimes spring from +rhizoids above ground, or from stems or leaves, are +<em>secondary</em>. The fact that a protonema can bud from parts +of the fruiting stems shows that the two do not belong to +different generations, but are merely successive stages of +a single generation, and both together compose the gametophyte.</p> + +<p id="p-397"><b>397. The leafy stage.</b>—In their fully developed state +the true mosses show a marked advance in organization over +the liverworts. There is a distinct +differentiation of the growing axis into +stem and leaves, though no true roots +are formed. The leaves are arranged +spirally, on upright stems, while in the +liverworts the vegetative body is +either a flat, spreading thallus, or the +leaves are arranged horizontally on +opposite sides of a prostrate, or more +or less inclined, axis. Sometimes a +second set occurs, on the upper side +of the axis, but in this case the leaves +are usually much smaller and inclined +to the horizontal arrangement, as +shown in <a href="#i_352">Fig. 484</a>.</p> + +<table class='autotable'> +<tr><td class="wd60"> +<figure class="figcenter illowp50" id="i_352" style="max-width: 30em;"> + <img class="w100" src="images/i_352.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 484.</span>—Scapania, a +liverwort with leafy thallus, approaching +the form of mosses +and lycopodiums. (<i>From</i> <span class="smcap">Coulter’s</span> +“Plant Structures.”)</p></figcaption> +</figure> +</td><td rowspan='2'> +<figure class="figcenter illowp60" id="i_353a" style="max-width: 30em;"> + <img class="w100" src="images/i_353a.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 486.</span>—Fruiting +stem of a moss +(<i>Polytrichum commune</i>) +with ripe capsules: +<i>s</i>, seta, or footstalk; +<i>c</i>, capsule with +calyptra; <i>f</i>, capsule +after the calyptra has +fallen away; <i>d</i>, operculum, +or lid.</p></figcaption> +</figure></td> +</tr> +<tr><td> +<figure class="figcenter illowp50" id="i_353" style="max-width: 30em;"> + <img class="w100" src="images/i_353.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 485.</span>—Fruiting receptacle +of a moss (<i>Phascum cuspidatum</i>), +bearing both antheridia, +<i>an</i>, and archegonia, <i>ar</i>, at +the bifurcated apex; <i>b</i>, leaves; +<i>p</i>, paraphyses.</p></figcaption> +</figure> +</td></tr></table> + +<p id="p-398"><b>398. The reproductive organs.</b>—The antheridia and +archegonia are borne in groups at the end either of the main<span class="pagenum" id="Page_343">[Pg 343]</span> +axes, or of lateral branches (<a href="#i_353">Figs. 485</a>, <a href="#i_353a">486</a>), but as a rule +only one archegonium is fertilized, so the mature sporogonia +are solitary. The plants may +be either diœcious or monœcious, as +in <a href="#i_353">Fig. 485</a>; and in +the latter case, the +reproductive organs +may be borne on the +same, or on different, +receptacles. The +antheridia and the +archegonia are both +mixed with club-shaped +hairs called +paraphyses (<a href="#i_353">Fig. +485</a>).</p> + +<p id="p-399"><b>399. The sporophyte.</b>—An examination +of the fruiting capsule of any of the true +mosses will show that it consists of a long +footstalk, the <em>seta</em>, <i>s</i>, <a href="#i_353a">Fig. 486</a>, bearing a +capsule, or ripened sporogonium, <i>f</i>, which +is at first surmounted by a cap or hood, +known as the <em>calyptra</em>, <i>c</i>. The hood represents +the excessively developed and often +highly specialized wall of the archegonium. +It falls away at maturity, and the spores are +discharged through an opening made by the +removal of the <em>operculum</em>, or lid, <i>d</i>. The +spores and the capsule are both developed +from the fertilized egg (oöspore), within the +archegonium, in much the same manner as in +the liverworts, and together constitute the +sporophyte, or asexual generation. It never +leads a completely independent existence, but remains a +partial parasite on the mother plant, though the lower part +of the young sporogonium is usually provided with stomata<span class="pagenum" id="Page_344">[Pg 344]</span> +and chlorophyll so that it is capable of manufacturing food. +In this respect it shows a distinct advance on the corresponding +phase of the liverworts—if we except the single genus +<i>Anthoceros</i>, which alone among the liverworts has the cells +of the sporogonium provided with chlorophyll.</p> + +<p id="p-400"><b>400. Alternation of generations.</b>—The process of reproduction +in mosses is so closely similar to that of liverworts +that it is unnecessary to repeat the details. There are +some minor variations, but in all essentials the processes +are the same and may be represented to the eye by the +same formula.</p> + +<p id="p-401"><b>401. Relative position of mosses and liverworts in the +line of evolution.</b>—Though mosses, as a rule, show a higher +degree of organization than liverworts, in both generations, +their development has been <em>away</em> from the general course +of evolution followed by the higher plants. This, as will +be seen later, tends towards a decreasing complexity of +the gametophyte with increasing complexity of the sporophyte, +while the mosses show increasing complexity of <em>both</em>. +Like the order of birds in the animal kingdom, they form +a highly specialized and somewhat isolated group. While +they may be regarded as descendants from a common ancestral +stock with the ferns and club mosses, they have +been switched off, so to speak, on a side track of the great +evolutionary trunk line, and their advance on this side +track has carried them to a point more remote from the +course along which the higher forms of plant life have +traveled than the distant junction at which they branched +off from their less progressive kindred, the humble liverworts.</p> + + +<h3 id="CH_X_VII">VII. FERN PLANTS</h3> + +<div class="blockquot"> + +<p><span class="smcap">Material.</span>—Any kind of fern in the fruiting stage. Several different +varieties should be cultivated in the schoolroom for observation. While +gathering specimens, look along the ground under the fronds, or in greenhouses +where ferns are cultivated, among the pots and on the floor, for +a small, heart-shaped body like that represented in <a href="#i_359">Figs. 501, 502</a>, called +a <em>prothallium</em>. It is found only in moist and shady places, and care should<span class="pagenum" id="Page_345">[Pg 345]</span> +be taken in collecting specimens, as in their early stages the prothallia +bear a strong resemblance to certain liverworts found in the same situations. +The best way is for each class to raise its own specimens by scattering +the spores of a fern in a glass jar, on the bottom of which is a bed +of moist sand or blotting paper. Cover the jar loosely with a sheet of +glass and keep it moist and warm, and not in too bright a light. Spores +of the sensitive ferns (<i>Onoclea</i>) will germinate in from two to ten days, +according to the temperature. Those of the royal fern (<i>Osmunda</i>) germinate +promptly if sown as soon as ripe, but if kept even for a few weeks +are apt to lose their vitality. The spores of sensitive fern can be kept +for six months or longer, while those of the bracken (<i>Pteris</i>) and various +other species require a rest before germinating, so that in these cases it +is better to use spores of the previous season.</p> +</div> + +<figure class="figright illowp50" id="i_355" style="max-width: 40em;"> + <img class="w100" src="images/i_355.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 487-491.</span>—A fern plant: 487, fronds +and rootstock; 488, fertile pinna: <i>s</i>, <i>s</i>, sori; +489, cross section of a stipe, showing ends of the +fibrovascular bundles; 490, a cluster of sporangia, +magnified; 491, a single sporangium still more +magnified, shedding its spores.</p></figcaption> +</figure> + +<p id="p-402"><b>402. Study of a typical fern.</b>—Observe the size and +general outline of the fronds, and note whether those of +the same plant are all alike, or if they differ in any way, +and how. Observe the +shape and texture of the +divisions or pinnæ composing +the frond, their +mode of attachment to +the rachis, and whether +they are simple, or +notched, or branched in +any way. Hold a pinna +up to the light and notice +the veining. Is it like any +of the kinds described in +<a href="#p-171">171</a>, <a href="#p-172">172</a>? In what respect +is it different? +This forked venation is +a very general characteristic +of ferns. When the +forks do not reticulate or +intercross, the veins are +said to be free; are they +free in your specimen, or +reticulated? Make a<span class="pagenum" id="Page_346">[Pg 346]</span> +sketch, labeling the primary branches of the frond, <em>pinnæ</em> +(sing., <em>pinna</em>), the secondary ones, if any, <em>pinnules</em>, and the +common stalk that supports them, <em>stipe</em>. Note the color, +texture, and surface of the stipe. If any appendages are +present, such as hairs, chaff, or scales (in Pteris, nectar +glands), notice whether they are equally distributed. If not, +where are they most abundant?</p> + +<p>Examine the mode of attachment of the stipes to their +underground axis. Break one away and examine the scar. +Compare with your drawings of leaf scars and with <a href="#i_101a">Fig. +105</a>. Do the stipes grow from a root or a rhizome? How +do you know? Do you find any remains of leafstalks of +previous years? How does the rootstock increase in +length? Measure some of the internodes; how much did +it increase each year? Cut a cross section and look for +the ends of the fibrovascular bundles. Trace their course +through several internodes. Do they run straight, or do +they turn or bend in any way at the nodes? If so, where +do they go? Do you see anything like roots? Where do +they originate? Put one of them under the microscope and +find out whether they are roots or hairs.</p> + +<p>True roots are first developed in the pteridophytes. Since +those of the fern spring from an underground stem, to what +class of roots do they belong? (83.)</p> + +<p id="p-403"><b>403. Minute study of a fern stem.</b>—Place a very thin +section of a fern rhizoma, or of the stipe of a frond, under +the microscope. Except in very young stems the vascular +bundles are arranged in a ring, or sometimes in two or +more rings (<a href="#i_357">Fig. 492</a>), with plates of strengthening tissue, +<i>l</i>, <i>l</i>, between the inner and outer rings. Notice the inner +epidermal layer of hard brown tissue, and within that, the +soft parenchyma, which fills the rest of the interior. Test +it with iodine and observe how rich in starch it is. If the +section of a petiole is under observation, the details will +be somewhat different; would you expect to find as much +starch in the stipe as in the rootstock? Why, or why not?</p> + +<p><span class="pagenum" id="Page_347">[Pg 347]</span></p> + + +<p>Make a longitudinal +section of a rhizome +through the point +where a leafstalk is +attached and trace the +course of the bundles. +This will be facilitated +if the specimen has +stood in eosin solution +a few hours. Make +enlarged drawings of +both sections, labeling +all the parts.</p> + +<table class='autotable'> +<tr><td class='wd60 vab'> +<figure class="figcenter illowp95" id="i_357" style="max-width: 30em;"> + <img class="w100" src="images/i_357.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 492.</span>—Diagram of a cross section through +the stem of a fern (<i>Pteris</i>): <i>s</i>, <i>s</i>, <i>s</i>, rings of fibrovascular +bundles; <i>l</i>, <i>l</i>, plates of strengthening tissue, +with a ring of fibrovascular bundles between them; +<i>lp</i>, zone of strengthening fibers; <i>r</i>, cortex; <i>e</i>, +epidermis.</p></figcaption> +</figure> +</td><td class='vab'> +<figure class="figcenter illowp95" id="i_357a" style="max-width: 30em;"> + <img class="w100" src="images/i_357a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 493-494.</span>—Parts of +fertile pinnæ: 493, of <i>polypodium</i>, +enlarged, showing the sori +without indusium; 494, of <i>pellea</i>, +showing indusium formed by the +revolute margin.</p></figcaption> +</figure></td></tr></table> + +<p>Clearly differentiated +conducting bundles +occur in the mosses, +but they are of much simpler structure than in the pteridophytes, +consisting usually of a single central strand, and are +found more frequently in the leaves +than in the stems. A true vascular +structure appears first in the pteridophytes, +whence these plants are +distinguished as <em>vascular cryptogams</em>.</p> + +<p id="p-404"><b>404. Fructification.</b>—Examine +the back of a fruiting frond; what +do you find there? These dots are +the <em>sori</em> (sing., <em>sorus</em>), or spore clusters, +and the fronds or pinnæ bearing +them are said to be <em>fertile</em>. Are +there any differences of size, shape, +etc., between the fertile and the +sterile fronds of your specimen? +between the fertile and the sterile pinnæ? On what part +of the frond are the fertile pinnæ borne? Notice the shape +and position of the sori, and their relation to the veins, +whether borne at the tips, in the forks, on the upper side<span class="pagenum" id="Page_348">[Pg 348]</span> +(toward the margin), or the lower (toward the midrib). +Look for a delicate membrane (<i>indusium</i>) covering the sori, +and observe its shape and mode of attachment. If the +specimen under examination +is a polypodium, there will be +no indusium; if a maidenhair, +or a bracken, it will be +formed of the revolute margin +of the pinna. In lady +fern and Christmas fern (<i>Aspidium</i>), +the sori frequently +become confluent, that is, so +close together as to appear +like a solid mass. Sketch a +fertile pinna as it appears under the lens, bringing out all +the points noted.</p> + +<figure class="figcenter illowp70" id="i_358" style="max-width: 30em;"> + <img class="w100" src="images/i_358.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 495-496.</span>—Christmas fern (<i>Aspidium</i>): +495, part of a fertile frond, natural +size; 496, a pinna enlarged, showing the +sori confluent under the peltate indusia.</p></figcaption> +</figure> + +<figure class="figcenter illowp90" id="i_358a" style="max-width: 50em;"> + <img class="w100" src="images/i_358a.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 497-500.</span>—Spores of pteridophytes, magnified: +497, a fern spore; 498, 499, two views of a spore of a club +moss; 500, spore of a common horsetail (<i>Equisetum arveuse</i>).</p></figcaption> +</figure> + +<p id="p-405"><b>405. The spore cases.</b>—Look under the indusium at +the cluster of little stalked circular appendages (<a href="#i_355">Fig. 490</a>). +These are the <em>sporangia</em>, or spore cases, in which the reproductive +bodies are borne. Place one of them under the +microscope, and it will be found to consist of a little stalked +circular body like a tennis racket (<a href="#i_355">Fig. 491</a>), surrounded +by a jointed ring +called the <em>annulus</em>. +Watch a +few moments and +see if you can +find out the use +of the annulus. +If not, warm the +slide and you will probably see the ring straighten itself +with a sudden jerk, rupturing the wall of the sporangium +and discharging the spores with considerable force. If this +does not happen, add a drop of strong glycerine to a specimen +mounted in water; the rupture will be apt to follow +quickly. What causes it, in either case? [<a href="#p-56">56</a>, (1); <a href="#exp-19">Exp. 19</a>.]</p> + +<p><span class="pagenum" id="Page_349">[Pg 349]</span></p> + +<p id="p-406"><b>406. The sporophyte.</b>—The spores found in such abundance +on the fertile pinnæ; are all alike, and each one is +capable of germinating and continuing the work of reproduction +as effectually as the sexual spores of the bryophytes. +The fertile frond, or part of a frond, on which they are borne +is called a <em>sporophyll</em> (spore-bearing leaf), and the entire +plant is the <em>sporophyte</em>, which, with its crop of spores, makes +up one generation.</p> + +<p>It is important to observe that in the ferns and in all pteridophytes +the sporophyte is the conspicuous and highly +organized body that is commonly recognized as the normal +growing plant; while with the bryophytes just the reverse +holds true,—the sexual generation, or gametophyte, represents +the normal plant structure, while the sporophyte is +an insignificant appendage +which never attains an +independent existence. +Broadly speaking, in bryophytes, +it is a spore fruit; +in the pteridophytes and +spermatophytes a highly +developed plant.</p> + +<figure class="figright illowp50" id="i_359" style="max-width: 50em;"> + <img class="w100" src="images/i_359.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 501, 502.</span>—Prothallium of a common +fern (<i>Aspidium</i>): 501, under surface, showing +rhizoids, <i>rh</i>, antheridia, <i>an</i>, and archegonia, +<i>ar</i>; 502, under surface of an older gametophyte, +showing rhizoids, <i>rh</i>, young sporophyte, +with root, <i>w</i>, and leaf, <i>b</i>.</p></figcaption> +</figure> + +<p id="p-407"><b>407. The gametophyte.</b>—When +one of these asexual +spores germinates, it +produces, not a fern plant +like the one that bore it, +but a small, heart-shaped +body like that shown in <a href="#i_359">Fig. 501</a>. Examine one of these bodies +carefully with a lens. Observe that there are no veins nor +fibrovascular bundles, and the whole body of the plant seems +to consist of one uniform tissue. Compare it with the forked +apex of a branching thallus of a liverwort. Do you perceive +any points of similarity? The two are, in fact, morphologically +the same. This heart-shaped body is called a <em>prothallium</em>, +and is the gametophyte of the fern. It may be of<span class="pagenum" id="Page_350">[Pg 350]</span> +different shapes, and in some species is branching and filamentous, +like the protonema of a moss. Generally, however, it +is flat and more or less two-lobed, as shown in <a href="#i_359">Fig. 501</a>. It +is small and inconspicuous and very short-lived, being of +importance only in connection with the work of reproduction.</p> + +<p>Look with your lens for a cluster of small, bottle-shaped +bodies just below the deep cleft in the heart. If you cannot +make out what they are, put a thin section through +a part of the prothallium containing one under the microscope, +and you will see that they are the archegonia. Lower +down among the rhizoids, near the pointed base, will be +found the antheridia. In some species the prothalli are +diœcious, one kind bearing antheridia, the other archegonia, +but this is rare among the true ferns.</p> + +<figure class="figright illowp50" id="i_360" style="max-width: 30em;"> + <img class="w100" src="images/i_360.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 503.</span>—Young archegonium of a fern, +magnified: <i>K</i>, neck canal cell; <i>K′</i>, ventral +canal cell: <i>O</i>, egg cell.</p></figcaption> +</figure> + +<p id="p-408"><b>408. Fertilization.</b>—This process is the same in all essentials +as in the bryophytes. As in other cryptogams, it can +take place only under +water,—a circumstance +which points to an aquatic +origin for this sub-kingdom, +and through them to the +entire flora of the globe. +The archegonia differ +somewhat in shape from +those of the liverworts and +mosses, but a section under +the microscope will show +that they consist of essentially +the same parts. On +account of the similarity of +these organs, the pteridophytes +and bryophytes are often classed together as <i>Archegoniates</i>.</p> + +<p id="p-409"><b>409. Alternation of generations.</b>—Among the section of +ferns that we have been considering, the order of alternation +corresponds in all essentials to that prevailing among the<span class="pagenum" id="Page_351">[Pg 351]</span> +bryophytes, and may be represented by the same formula. +The chief difference is in the relatively much greater importance +of the sporophyte, which may be expressed by +putting it first:—</p> + +<table class="autotable fs80 alternation"> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"><i>S</i> ⟶ <i>o</i> ⟶ <i>G</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"> <i>oös</i> ⟶ <i>S</i> ⟶ <i>o</i> ⟶ <i>G</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>oös</i> ⟶ <i>S</i> ⟶ <i>o</i> ⟶ <i>G</i> etc.</td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +</table> + +<p>But some of the pteridophytes—of which the Selaginella +offers a conspicuous example—have differentiated their<span class="pagenum" id="Page_352">[Pg 352]</span> +asexual spores (<i>o</i> of the formula) into two kinds, large and +small, known respectively as <em>megaspores</em> and <em>microspores</em>. +The prothallia developed by the former bear archegonia +containing female gametes only; those by the latter, antheridia +containing male gametes—while in the diœcious bryophytes, +the archegonial and antheridial thalli are produced +by spores of the same kind.</p> + +<figure class="figcenter illowp74" id="i_361" style="max-width: 75em;"> + <img class="w100" src="images/i_361.jpg" alt=""> + <figcaption><p><span class="smcap">Figs. 504.-508.</span>—A kind of pteridophyte (<i>Selaginella martensii</i>) with its organs of +fructification: 504, a fruiting branch; 505, a microsporophyll with a microsporangium, +showing microspores through a rupture in the wall; 506, a megasporophyll +with a megasporangium; 507, megaspores; 508, microspores. (<i>From</i> <span class="smcap">Coulter’s</span> +“Plant Structures.”)</p></figcaption> +</figure> + +<p>The differentiation of the asexual spores in the higher +pteridophytes gives rise to corresponding changes in the +sporangia that bear them, and even in the sporophylls themselves, +one kind bearing microsporangia only, the other +megasporangia. In this way the differentiation of sex is +pushed back, step by step, until it virtually begins with the +sporophyte, or asexual generation.</p> + +<p>Using the same terms as before, and representing the microspores +by the abbreviation <i>mo</i>, the megaspores by <i>Mo</i>, +the archegonial gametophyte by <i>arG</i>, the antheridial by +<i>anG</i>, the formula may be modified to express this more complicated +process of alternation, as follows:—</p> + +<table class="autotable fs80 alternation"> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>Mo</i> ⟶ <i>arG</i> ⟶ <i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>Mo</i> ⟶ <i>arG</i> ⟶ <i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"><i>S</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"> <i>oös</i> ⟶ <i>S</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>oös</i> ⟶ <i>S</i> etc.</td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mo</i> ⟶ <i>anG</i> ⟶ <i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mo</i> ⟶ <i>anG</i> ⟶ <i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +</table> + +<p class="noindent">Comparing this formula with the preceding, it will be seen +that the increased complexity affects the sporophyte at the +expense of the gametophyte, which has now become a mere +dependent on the former.</p> + +<p id="p-410"><b>410. Advantages of alternation.</b>—This roundabout mode +of reproduction would hardly have been developed unless it +had been of some benefit to the plants in which it occurs. +The chief advantage seems to be in more rapid multiplication +and consequently better chance to propagate the species, as +compared with the slow process of sexual reproduction were +the plant confined to that method alone. Only one plant is +produced by each oöspore, and if this were a gametophyte +with its limited number of archegonia, multiplication would<span class="pagenum" id="Page_353">[Pg 353]</span> +be slow; but the sporophyte with its millions of spores, each +capable of producing a new individual, enables the species to +multiply indefinitely. At the same time the interposition of +a gametophyte, or sexual generation, secures the introduction +of a new strain with effects analogous to those of cross +fertilization.</p> + +<figure class="figright illowp20" id="i_363" style="max-width: 20em;"> + <img class="w100" src="images/i_363.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 509.</span>—Part +of the fruiting +stem of a +scouring rush, +<i>Equisetum limosum</i>, +showing the +cone-like spore +cluster. (<i>After</i> +<span class="smcap">Gray</span>.)</p></figcaption> +</figure> + +<p id="p-411"><b>411. Classification of pteridophytes.</b>—In our study of +this group, the ferns have been taken as the type because +they are the most familiar and most widely +distributed of all the vascular cryptogams. +But while they exceed in numbers, both of +individuals and species, all the other orders +combined, they form only one division of three +great groups that make up the class Pteridophyta. +These groups are: (1) ferns, under +which are included, besides the true ferns, two +widely differing orders, with the grape ferns +and adder’s-tongue in one, and the water ferns +in the other; (2) the club mosses, embracing +the two subdivisions of <i>Lycopodium</i> and <i>Selaginella</i>; +(3) the horsetail family, including +horsetails and scouring rushes. Orders (2) +and (3) are grouped together as cone-bearing +(strobilaceous) pteridophytes, because their +sporangia are clustered in oblong heads, or +<em>strobiles</em> (<a href="#i_363">Fig. 509</a>), somewhat like the cones of +the pine. The orders of pteridophytes differ +greatly among themselves, but agree in possessing +certain characteristics that point to +their derivation from a common ancestry.</p> + +<p id="p-412"><b>412. Distinction between pteridophytes and +bryophytes.</b>—In passing from the Thallophytes +and Bryophytes to the vascular cryptogams, we cross +the widest chasm in the vegetable kingdom—a gap relatively +as great as that between vertebrates and invertebrates among +animals. The most important modifications that discriminate<span class="pagenum" id="Page_354">[Pg 354]</span> +the two groups are: (1) the presence in Pteridophytes +of a highly organized vascular system accompanied by a +well-marked differentiation of the plant body into root and +stem; (2) increased importance and complexity of the sporophyte +with proportionate diminution of the gametophyte.</p> + +<p>While vessels for conducting water occur in some of the +bryophytes <a href="#p-403">(403)</a>, a well-defined vascular system and true +roots are met with first in the Pteridophytes. The change +in the relative importance of sporophyte and gametophyte +is so marked that in Selaginella, the genus which approaches +nearest in structure to the seed-bearing plants, the suppression +of the gametophyte has proceeded so far that it never +leads an independent existence at all and is difficult even to +recognize as a distinct individual.</p> + + +<h4>Practical Questions</h4> + +<div class="blockquot"> + +<p>1. Have ferns any economic use—that is, are they good for food, +medicines, etc.?</p> + +<p>2. What is their chief value?</p> + +<p>3. Under what ecological conditions do they grow?</p> + +<p>4. Are they often attacked by insects, or by blights and disease of +any kind?</p> + +<p>5. Of what advantage is it to ferns to have their stems underground, +in the form of rootstocks? (<a href="#p-321">321</a>.)</p> + +<p>6. What causes the young frond of ferns to unroll? (<a href="#p-54">54</a>, <a href="#p-98">98</a>.)</p> + +<p>7. Name the ferns indigenous to your neighborhood.</p> + +<p>8. Which of these are most ornamental, and to what peculiarities of +structure do they owe that quality?</p> + +<p>9. Are cultivated ferns usually raised from the spores or in some +other way? Why?</p> + +<p>10. After the great eruption of <a id="tn_354">Krakatoa</a> in 1883, by which the vegetation +of the island was completely destroyed, ferns were the first plants +to reappear. Explain why. (<a href="#p-19">19</a>; <a href="#exp-17">Exp. 17</a>.)</p> +</div> + + +<h3 id="CH_X_VIII">VIII. THE RELATION BETWEEN CRYPTOGAMS AND +SEED PLANTS</h3> + +<p id="p-413"><b>413. No break in the chain of life.</b>—The great gap that +was once supposed to exist between the cryptogams and +phanerogams has been bridged over by the discovery of<span class="pagenum" id="Page_355">[Pg 355]</span> +analogies in the reproductive processes of the two groups +that connect them together as successive links in one continuous +chain of vegetable life. It is therefore very important +to have a clear understanding of the nature and meaning of +these processes, for the chief turning points in the life history +of the different groups of plants are connected with +them, their natural relationships to each other, and their +distribution according to their respective places in the evolutionary +scale, being determined largely by a comparison of +their modes of continuing the life of the group.</p> + +<p id="p-414"><b>414. Alternation of generations in seed plants.</b>—This +process, so conspicuous among Bryophytes and Pteridophytes, +and not unknown among Thallophytes, is universal +among seed plants (Spermatophytes) also, though in so +masked a form that it is not easy to recognize without a +more detailed study than would be practicable within the +limits of a book like this. Briefly, we may say that the +stamens of spermatophytes, and the pistils, or rather the +carpels, which we have seen to be transformed leaves <a href="#p-298">(298)</a>, +represent the sporophylls <a href="#p-406">(406)</a> of the higher pteridophytes. +The pollen sacs and ovules are sporangia, bearing microspores +and megaspores <a href="#p-409">(409)</a>, represented respectively by +the pollen grains in the anther and the embryo sac in the +ovule. These go through a series of microscopic changes in +the body of the ovule analogous to the production of the +oöspore in the archegonia of ferns and liverworts, but the +process is so obscure that to an ordinary observer the pollen +grains and the ovule appear to be the real gametes, and were +long supposed to be such. The fertilized germ cell in the +embryo sac <a href="#p-251">(251)</a> corresponds to an oöspore; the embryo sac +with the endosperm found in all seeds (previous to its absorption +by the cotyledons) is a rudimentary gametophyte; and +the embryo in the matured seed is the undeveloped sporophyte, +destined, after germination and further growth, to +produce a new generation with its recurrent cycle of alternating +phases.</p> + +<p><span class="pagenum" id="Page_356">[Pg 356]</span></p> + +<figure class="figleft illowp50" id="i_366" style="max-width: 40em;"> + <img class="w100" src="images/i_366.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 510.</span>—Diagrammatic section through the +ovule of a gymnosperm belonging to the spruce +family: <i>i</i>, integument covering the ovule; <i>e</i>, endosperm +(corresponding to female gametophyte), +which fills the embryo sac, containing two archegonia, +<i>a</i>; <i>o</i>, egg cell; <i>p</i>, pollen grains; <i>t</i>, pollen +tubes entering the neck, <i>c</i>, of the archegonia.</p></figcaption> +</figure> + +<p>In the gymnosperms,—pines, yews, cycads, etc.,—which +represent the most ancient and primitive type of existing +seed-bearing plants, +the similarity of these +processes to those of +certain of the pteridophytes +is very striking, +and it was through +the study of these that +the sequences of the +process were traced in +the much more obscure +form in which they +occur among the angiosperms. +From the +endosperm in the seeds +of gymnosperms archegonia +were found to be +developed (<a href="#i_366">Fig. 510</a>) in +much the same way as +in Selaginella, from the +prothallium, thus +showing the endosperm +to be a modified +and greatly reduced +gametophyte. In some cases, it has even been found to +protrude a little way out of the embryo sac and to take on +a slightly greenish tinge—another reminiscence of its origin. +Fertilization, too, takes place in precisely the same manner +as in the pteridophytes, except that in all but the ginkgo +and the cycads, the fertilizing cells in the pollen grains are +non-motile, and find their way to the ovule by growing down +into the embryo sac with the pollen tube, instead of swimming +to it—an adaptation probably brought about in response +to changed condition during the course of evolution from +aquatic to terrestrial life.</p> + +<p><span class="pagenum" id="Page_357">[Pg 357]</span></p> + +<p>The analogies between the sequence of alternations in the +two classes will be made clearer by a comparison of the +accompanying diagrams. The corresponding terms applied +to the various organs stand in the same vertical row. Diagram +(1) shows the process as it takes place in the more +highly developed Pteridophytes; diagram (2) the corresponding +phases in angiosperms.</p> + +<p class="center fs80 cb">PTERIDOPHYTES</p> + +<table class="autotable fs80 alternation"> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>mospl</i> ⟶ <i>mic</i> ⟶ <i>mo</i> ⟶ <i>anG</i> ⟶ <i>ant</i> ⟶ <i>mg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc">(1) <i>S</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"> <i>öos</i> ⟶ <i>S</i></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>Mospl</i> ⟶ <i>Mgc</i> ⟶ <i>Mo</i> ⟶ <i>arG</i> ⟶ <i>arc</i> ⟶ <i>fg</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr></table> + +<div class='mth'> +<p class="fs80"><i>mospl</i>, microsporophyll; <i>mic</i>, microsporangium; <i>mo</i>, microspores; <i>anG</i>, male +gametophyte; <i>ant</i>, antheridia; <i>mg</i>, antherozoids. The letters in the lower line +stand for the corresponding female organs.</p></div> + + +<p class="p2 center fs80">SPERMATOPHYTES</p> + +<table class="autotable fs80 gymnosperms"> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc vac"><i>st</i> ⟶ <i>an</i> ⟶ <i>pol</i> ⟶ <i>fc</i> ⟶</td> +<td class='tdc vac'><i>not<br>developed</i></td> +<td class='tdc vac'> ⟶ <i>gc</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc">(2) <i>S</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"> <i>öos</i> ⟶ <i>S</i></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc">╲</td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc">╱</td> +<td class="tdc"></td> +</tr> +<tr> +<td class="tdc"></td> +<td class="tdc"></td> +<td class="tdc"><i>p</i> ⟶ <i>ov</i> ⟶ <i>em</i> ⟶ <i>end</i> ⟶</td> +<td class='tdc vac'><i>developed<br>only in<br>gymnosperms</i></td> +<td class='tdc vac'> ⟶ <i>ec</i></td> +<td class="tdc"></td> +<td class="tdc"></td> +</tr></table> + +<p class="fs80"><i>st</i>, stamen; <i>an</i>, anther; <i>pol</i>, pollen; <i>fc</i>, food cells in pollen grain; <i>gc</i>, generative +cell; <i>p</i>, pistil; <i>ov</i>, ovules; <i>em</i>, embryo sac; <i>end</i>, endosperm; <i>ec</i>, egg cell.</p> + +<p id="p-415"><b>415. Disappearance of the gametophyte.</b>—The seed is a +comparatively recent development in plant evolution. It +has no counterpart anywhere among the cryptogams, but is +strictly characteristic of the three great orders of Spermophytes: +Monocotyl, Dicotyl, and Gymnosperms, which +compose the greater part of the vegetation of the globe. +Structurally, it is a matured sporangium containing a rudimentary +sporophyte (the embryo), and a reduced gametophyte +(the embryo sac), which, under the form of endosperm, +has dwindled to an insignificance that makes it difficult to +recognize it as a phase in an alternation of generations.</p> + +<p id="p-416"><b>416. Significance of the sporophyte.</b>—The gametophyte +is obviously a more ancient and primitive structure than the +sporophyte, which first becomes prominent in the ferns and<span class="pagenum" id="Page_358">[Pg 358]</span> +their allies. The sudden and violent break in the succession +of vegetable life that accompanies the appearance of the +pteridophytes <a href="#p-412">(412)</a> is probably to be explained by the +development of a land flora and the necessity of adaptation to +life in a new medium. The fact that no living cell, whether +vegetable or animal, can absorb nourishment except in a +liquid form, seems to point to an aquatic origin more or less +remote for all life. This inference is further strengthened, +in the case of plants, by the fact that even in so highly organized +a group as the pteridophytes, fertilization cannot +take place except in water. Such a requirement would +manifestly be a great disadvantage to land plants, and one +of the first steps in response to the demands of a new habitat +would be to get rid, as far as possible, of the primitive gametophyte +with its outgrown adaptations to a liquid medium, +and to transfer the greater part of the work of reproduction +to the asexual generation, in which the problem of fertilization +did not have to be directly met, the asexual spores germinating +without it. The greater the number of these +produced, the better the chance that at least some of the +gametes developed from them would meet the difficult conditions +of fertilization, and the survival of the species be +assured. At the same time, in order to meet the requirements +of terrestrial life successfully, and to provide for continuing +the sexual generation, correlative changes would have to +take place in the gametophyte by which the increasing +uncertainty of fertilization due to structural changes in the +sporophyte, and the absence of a liquid medium for the conveyance +of free swimming antherozoids would be avoided. +This necessity has been met by the development of the pollen +tube, which bores its way to the egg cell, carrying with it the +generative cells, which in seed plants have taken the place +of the more primitive antherozoids. With the concomitant +reduction of the gametophyte and development of the seed +habit, the adaptation to land conditions has been made +complete.</p> + +<p><span class="pagenum" id="Page_359">[Pg 359]</span></p> + +<p>Roughly speaking, it may be said: (1) that Thallophytes +are predominantly aquatic; (2) Archegoniates (Bryophytes +and Pteridophytes), amphibious; (3) Spermophytes, terrestrial; +(4) that the seed habit is a response to terrestrial +conditions; and (5) that the increased development of the +sporophyte was a necessary adaptation to meet those conditions.</p> + + +<h3 id="CH_X_IX">IX. THE COURSE OF PLANT EVOLUTION</h3> + +<p id="p-417"><b>417. Plant genealogy.</b>—It has been shown by a study of +existing forms of plant life that there is no hard and fast +line of division anywhere between the different groups, but +that they are all connected by ties of kinship more or less +defined, according to their distance from a common ancestral +stock. The geological record points to the same conclusion, +and our classification of them into families, orders, and species +is merely a very imperfect genealogical table of their +supposed pedigrees. This does not mean, however, that we +can assert positively that such and such a species is derived +from such or such another, but that both are descended from +some common intermediate form more or less remote. While +we have reason to believe that the flowering plants are derived +through pteridophyte and bryophyte types from some +of the green algæ, no direct connection has ever been traced +between any particular kind of flowering plant and any particular +kind of alga,—or between a liverwort and an alga, +for that matter,—and probably never will be, because the intermediate +forms die out, or pass on by variation into other +lines of development. But while this is true, all the evidence +we possess does go to show that, since the beginning of life +on the globe, there has been a general progressive evolution +from lower and simpler to higher and more complex forms.</p> + +<p id="p-418"><b>418. Retrogressive evolution.</b>—While the general course +of evolution has been upward and onward, the movement has +not always followed a straight line, but, like a mountain road,<span class="pagenum" id="Page_360">[Pg 360]</span> +shows many windings and deviations from the direct route. +The monocotyls furnish a conspicuous example of this departure +from the general law of progression. It was formerly +supposed, on account of their greater simplicity of structure, +that they were a more ancient type than dicotyls, but recent +investigations point to the conclusion that they are a later +offshoot, derived from some primitive form of aquatic dicotyl, +and represent, not an ancient and primitive stock, but a case +of retrogressive evolution from a higher type. Strong presumptions +in favor of this view are: (1) that various species +of dicotyls show an unequal development of the seed leaves, +amounting, in the bryony, to complete abortion of one of +them, while some monocotyl seeds show morphological +characters that can best be explained as survivals, or inheritances, +from a dicotyl ancestor; (2) the structural resemblances +between gymnosperms and dicotyls are closer than +between gymnosperms and monocotyls, which could hardly +be the case if the latter were the more ancient; (3) the geological +record does not show them to have appeared before +dicotyls; (4) the number of cotyledons furnishes no criterion +as to the relative age of any plant group, since all three types +are represented among the pteridophytes, where plants are +found bearing one, two, or more cotyledons.</p> + +<p>The theory of their comparatively recent origin from an +aquatic ancestor is further borne out by the many points of +similarity between their internal structure and that of hydrophytes +<a href="#p-318">(318)</a>, and also by the great proportion of aquatic +plants among them, amounting to thirty-three per cent, while +in dicotyls the proportion is only four per cent. Can you +give any reasons, from your examination of their internal +structure (<a href="#p-113">113</a>, <a href="#p-114">114</a>), for believing that the line of development +which they have followed is a less effective one for +meeting conditions now existing on the globe than that attained +by dicotyls?</p> + +<p>We should remember, too, that while progressive evolution +implies successful adjustment to surroundings, it is possible<span class="pagenum" id="Page_361">[Pg 361]</span> +to conceive of a state, as our planet approaches the period +of cosmic debility and decay, when the conditions of existence +may become progressively more and more unfavorable. In +this case the course of evolution would be reversed, the higher +types gradually dying out as the struggle for life became +more severe, and the tendency would be constantly toward +lower and simpler forms, until finally all life would become +extinct on our planet. +We have no right, however, +to assume that +during such a course of +retrogressive evolution +the same forms would +be repeated in reverse +order as have already +appeared, because +there is no reason to +believe that the conditions +brought about by +planetary decline and +“old age” would be +the same as those attending +planetary +birth and adolescence.</p> + +<figure class="figright illowp50" id="i_371" style="max-width: 40em;"> + <img class="w100" src="images/i_371.jpg" alt=""> + <figcaption><p><span class="smcap">Fig. 511.</span>—Diagram showing the supposed +course of plant evolution.</p></figcaption> +</figure> + +<p id="p-419"><b>419. Explanation of +the diagram.</b>—An attempt +to show the +general course of plant +evolution up to the present time is made in the accompanying +diagram. The four great divisions, Thallophytes, Bryophytes, +Pteridophytes, and Spermatophytes, are represented +by spaces between four horizontal lines arranged one above +the other in the order of their succession in time and complexity +of organization. It should be borne in mind that +these dividing lines are not sharply defined in nature, but +overlap or indent the territory between them with varying<span class="pagenum" id="Page_362">[Pg 362]</span> +degrees of irregularity, like the coast line on a map. +The relative positions of the different orders we have +been considering are represented by upright and diagonal +lines, the general course of which, as indicated by the +arrows, is intended to give an idea of the trend of evolutionary +progress in the particular group represented by each +line. No one of these lines is made to originate directly in +any other, because, with the possible exception of the monocotyls, +we have no authority for asserting that any such direct +connection exists between plants as we know them, but only +that certain types give evidence of descent from a common +ancestry. This lack of certainty is expressed by placing the +point of origin for any given line in more or less close proximity +to the one which is supposed to be the nearest living +representative of the common ancestor. The line of ferns, +for instance, is depicted as originating in the region of the +bryophytes, somewhere in the neighborhood of the liverworts, +but the two lines nowhere come in contact, because there is +no evidence that any fern, living or fossil, is directly descended +from any particular kind of liverwort known to us. +With these explanations, the diagram shows, in a rough way, +the generally accepted view of plant relationships as based on +the evidence at present before us. But in questions of this +sort it is wise to keep in mind the blunt remark of a famous +old American statesman, that “only fools and dead people +never change their opinions.”</p> + + +<h4 id="CH_X_FIELD">Field Work</h4> + +<div class="blockquot"> + +<p>1. If you live in the country, study the appearance of plants affected +with blights, smuts, rusts, and mildews, and learn to recognize the different +kinds of disease by their signs. Notice which kinds are most prevalent in +your neighborhood, and what plants are most affected by them.</p> + +<p>2. Notice the different kinds of mushrooms you find growing wild. +Observe the difference between those that grow on the ground and those +that grow on logs, stumps, and trees; between those found in the woods +and those in open ground. Find out how those on the ground get their +nourishment. Uncover the mycelium, and notice the extent of its surface.<span class="pagenum" id="Page_363">[Pg 363]</span> +Examine the soil and find out if it contains anything upon which they +could feed. Note the prevalence of shelf fungi on trees. Examine the +condition of the wood where they grow, and decide in what ways they +injure their hosts. Notice whether they abound most on healthy or on +decaying trunks and boughs, and decide whether this is because the +fungus prefers that kind of host, or whether the injury it does causes +the decay, or whether both causes operate together. Notice what fungi +grow on different trees, and study their preferences in this respect.</p> + +<p>3. Observe the different kinds of lichens found in your walks and try +to distinguish the three classes. Which kind are most abundant in your +neighborhood? Which least so? Note the situations in which you find +each kind growing, whether on stumps, trees, rocks, or the ground. Consider +how the algæ and fungi aid each other in the different positions; +could either, for instance, exist independently on bald rocks? Notice on +what kind of trees the different lichens seem to thrive best and on which +poorly or not at all, and whether the character of the bark—rough, +smooth, scaly—has anything to do with their choice of a habitat.</p> +</div> +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_364">[Pg 364]</span></p> + +<h2 class="nobreak" id="APPENDIX">APPENDIX</h2> +</div> + +<h3 id="APP_1">SYSTEMATIC BOTANY</h3> + + +<p><b>Taxonomy, or systematic botany</b>, deals with the family +relationships of plants in the order of their nearness or remoteness +with regard to a common line of descent. Its chief +value is the insight it gives into the course of plant evolution +and into the nature of the modifications that differentiate +each group from the ancestral type. While it is not advisable +to spend too much time in the mere identification of +species, a sufficient number should be examined and described +to familiarize the student with the distinctive +characteristics of the principal botanical orders.</p> + +<p><b>Principles of classification.</b>—All the known plants in the +world, numbering not less than one hundred and twenty +thousand species of the seed-bearing kind alone, are ranged +according to certain resemblances of structure, into a number +of great groups known as families or orders. The names +of these families are distinguished by the ending <em>aceæ</em>; the +rose family, for instance, are the <i>Rosaceæ</i>; the pink family, +<i>Caryophyllaceæ</i>; the walnut family, <i>Juglandaceæ</i>, etc. Each +of these families is divided into lesser groups called <em>genera</em> +(singular, <em>genus</em>), characterized by similarities showing a +still greater degree of affinity than that which marks the +larger groups or orders; and finally, when the differences +between the individual plants of a kind are so small as to be +disregarded, they are considered to form one species; all the +common morning-glories, for instance, of whatever shade or +color, belong to the species <i>Ipomea purpurea</i>. The small +differences that arise within a species as to the color and<span class="pagenum" id="Page_365">[Pg 365]</span> +size of flowers, and other minor points, constitute mere +varieties, and have no special names applied to them. The +line between varieties and species is not clearly defined, and +in the nature of things can never be, since progressive development, +through unceasing change, is the law of all +life.</p> + +<p>In botanical descriptions, the name both of the species +and the genus is given, just as in designating a person, like +Mary Jones or John Robinson, we give both the surname +and the Christian name. The genus, or generic name, +answers to the surname, and that of the species to the +Christian name—except that in botanical nomenclature +the order is reversed, the generic, or surname, coming first, +and the specific or individual name last; for example, +<i>Ipomea</i> is the generic, or surname, of the morning-glories, and +<i>purpurea</i> the specific one.</p> + +<p><b>How to use the key.</b>—Any good manual will answer the +purpose. Gray’s “School and Field Book” is, perhaps, the +best available at present for the states east of the Mississippi. +Reference to the floral analyses in sections <b>I-IV</b> of +Chapter VII will make its use clear. Suppose, for instance, +we want to find out to what botanical species the morning-glory +or the sweet potato belongs. Turning to the key, +we find the sub-kingdom of Phænerogams—flowering or +seed-bearing plants—divided into two great classes, Angiosperms +and Gymnosperms, as explained in 18. A glance will +show that our specimen belongs to the former class. Angiosperms, +again, are divided into the two subclasses of Dicotyledons +and Monocotyledons (<a href="#p-18">18</a>, <a href="#p-171">171</a>). We at once recognize +our plant, by its net-veined leaves and pentamerous flowers, +as a dicotyledon (<a href="#p-171">171</a>, <a href="#p-229">229</a>), and turning again to the key, +we find this subclass divided into three great groups: Sympetalous +<a href="#p-211">(211)</a>, called also Monopetalous and Gamopetalous; +Apopetalous, or Polypetalous <a href="#p-211">(211)</a>, and Apetalous—having +no petals or corolla. A glance will refer our blossom to the +sympetalous or monopetalous group, which we find divided<span class="pagenum" id="Page_366">[Pg 366]</span> +into two sections, characterized by the superior or inferior +ovary (<a href="#p-218">218</a>, <a href="#p-225">225</a>). Further examination will show that the +morning-glory belongs to the former class, which is in turn +divided into two sections, according as the corolla is <em>regular</em>, +or <em>more or less irregular</em>. We see at once that we must look +for our specimen in the group having regular corollas. This +we find again subdivided into four sections, according to the +number and position of the stamens, and we find that the +morning-glory falls under the last of these,—“Stamens as +many as the lobes or parts of the corolla and alternate +with them.” A very little further search brings us to the +family <i>Convolvulaceæ</i>, and turning to that title in the descriptive +analysis, we find under the genus, <i>Ipomea</i>, a full +description of the common morning-glory, in the species +<i>Ipomea purpurea</i>, and of the sweet potato in the species +<i>Ipomea batatas</i>.</p> + +<p><b>Making collections.</b>—Mere labeled aggregations of species +are not recommended, but the collection of examples illustrating +special points in morphology and plant variation +may be made with profit; such, for instance, as the adaptations +observed in tendrils and stipular appendages, the +various modifications of leaves and stems to serve other +than their normal purposes, or the different forms of leaves +and flowers on the same stem, or on different plants of the +same species. A collection made with some specific object +in view would also be instructive, and might prove of great +value; for instance, to get together examples of all the +troublesome weeds of a locality for the purpose of studying +their habits and devising means for their eradication; or of +all the native useful plants, with detailed analyses of their +economic properties, and observations on their habits and the +practicability of further developing them. In short, wherever +collecting is carried on, it should be done with some object +other than the mere identification of species, which often +results in greater detriment to the wild plants of a neighborhood +than profit to the collector.</p> + +<p><span class="pagenum" id="Page_367">[Pg 367]</span></p> + + +<h3 id="APP_2">WEIGHTS, MEASURES, AND TEMPERATURES</h3> + +<p>As the metric system of weights and measures and the +Centigrade appraisement of temperatures are universally +employed in scientific works, the following tables showing +the equivalents in our common English standards of those +in most frequent use, are given for the convenience of +students who have not already familiarized themselves with +the subject. The values given are approximate only, but will +answer for all practical purposes, except in cases where very +great exactitude is required. The micron, or micrometer, +is used principally by scientific investigators for measuring +extremely minute objects seen under the microscope.</p> + + +<p class="p2 center fs80"><span class="smcap">Measures of Length</span></p> + + +<table class="autotable fs80 wd80"> +<tr><td class="bt" colspan="3"></td></tr> +<tr><td class="bt" colspan="2"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdc smcap" colspan="2">Metric</td> +<td class="tdc bl smcap">English Equivalents</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Kilometer</td> +<td class="tdl bl wd20">km.</td> +<td class="tdl bl wd50">⅔ of a mile.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Meter</td> +<td class="tdl bl">m.</td> +<td class="tdl bl">39 inches.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Decimeter</td> +<td class="tdl bl">dm.</td> +<td class="tdl bl">4 inches.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Centimeter</td> +<td class="tdl bl">cm.</td> +<td class="tdl bl">⅖ of an inch.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Millimeter</td> +<td class="tdl bl">mm.</td> +<td class="tdl bl">¹⁄₂₅ of an inch.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Micron</td> +<td class="tdl bl">µ</td> +<td class="tdl bl">¹⁄₂₅₀₀₀ of an inch.</td> +</tr> +<tr><td class="bb"></td><td class="bb bl"></td><td class="bb bl"></td></tr> +</table> + +<p class="p2 center fs80"><span class="smcap">Capacity</span></p> + +<table class="autotable fs80 wd80"> +<tr><td class="bt" colspan="3"></td></tr> +<tr> +<td class="tdl">Liter</td> +<td class="tdl bl wd20">l.</td> +<td class="tdl bl wd50">61 cubic inches, or 1 quart, U.S. measure</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl">Cubic centimeter</td> +<td class="tdl bl">cc.</td> +<td class="tdl bl">¹⁄₁₆ of a cubic inch.</td> +</tr> +<tr><td class="bb"></td><td class="bb bl"></td><td class="bb bl"></td></tr> +</table> + +<p class="p2 center fs80"><span class="smcap">Weight</span></p> + +<table class="autotable fs80 wd80"> +<tr><td class="bt" colspan="3"></td></tr> +<tr> +<td class="tdl">Kilogram</td> +<td class="tdl bl wd20">kg., or kilo.</td> +<td class="tdl bl wd50">2⅕ pounds.</td> +</tr> +<tr><td class="bt"></td><td class="bt bl"></td><td class="bt bl"></td></tr> +<tr> +<td class="tdl" rowspan="2">Gram</td> +<td class="tdl bl" rowspan="2">gm.</td> +<td class="tdl bl">15½ grains avoirdupois.</td> +</tr> +<tr> +<td class="tdl bl">¹⁄₂₈ of an ounce avoirdupois.</td> +</tr> +<tr><td class="bb"></td><td class="bb bl"></td><td class="bb bl"></td></tr> +<tr><td class="bb" colspan="3"></td></tr> +</table> + +<p><span class="pagenum" id="Page_368">[Pg 368]</span></p> + + +<p class="p2 center fs80"><span class="smcap">Metric and English Scales</span></p> + +<figure class="figcenter illowp75" id="i_378" style="max-width: 50em;"> + <img class="w100" src="images/i_378.jpg" alt="Rulers comparing millimeters to inches"> + <figcaption><p class='center'>10 CENTIMETERS = 1 DECIMETER<br> + 100 MILLIMETERS<br> + 4 INCHES</p></figcaption> +</figure> + +<p class="p2 center fs80"><span class="smcap">Temperature Equivalents</span></p> + +<p>The next table gives the Fahrenheit equivalent, in round +numbers, for every tenth degree Centigrade from absolute +zero to the boiling point of water. To find the corresponding +F. for any degree C., multiply the given C. temperature +by nine, divide by five, and add thirty-two. Conversely, +to change F. to C. equivalent, subtract thirty-two, multiply +by five, and divide by nine.</p> + +<table class="autotable fs80 wd20"> +<tr> +<th class="tdc wd50">Cent.</th> +<th class="tdc wd50">Fahr.</th> +</tr> +<tr><td class="bb" colspan="2"></td></tr> +<tr> +<td class="tdr">100</td> +<td class="tdr">212</td> +</tr> +<tr> +<td class="tdr">90</td> +<td class="tdr">194</td> +</tr> +<tr> +<td class="tdr">80</td> +<td class="tdr">176</td> +</tr> +<tr> +<td class="tdr">70</td> +<td class="tdr">158</td> +</tr> +<tr> +<td class="tdr">60</td> +<td class="tdr">140</td> +</tr> +<tr> +<td class="tdr">50</td> +<td class="tdr">122</td> +</tr> +<tr> +<td class="tdr">40</td> +<td class="tdr">104</td> +</tr> +<tr> +<td class="tdr">30</td> +<td class="tdr">86</td> +</tr> +<tr> +<td class="tdr">20</td> +<td class="tdr">68</td> +</tr> +<tr> +<td class="tdr">10</td> +<td class="tdr">50</td> +</tr> +<tr> +<td class="tdr">0</td> +<td class="tdr">32</td> +</tr> +<tr> +<td class="tdr">−10</td> +<td class="tdr">14</td> +</tr> +<tr> +<td class="tdr">−20</td> +<td class="tdr">−4</td> +</tr> +<tr> +<td class="tdr">−30</td> +<td class="tdr">−22</td> +</tr> +<tr> +<td class="tdr">−40</td> +<td class="tdr">−40</td> +</tr> +<tr> +<td class="tdr">−50</td> +<td class="tdr">−58</td> +</tr> +<tr> +<td class="tdr">−100</td> +<td class="tdr">−148</td> +</tr> +<tr> +<td class="tdc bt" colspan="2">Absolute zero.</td> +</tr> +<tr> +<td class="tdr">-273</td> +<td class="tdr">-459</td> +</tr> +</table> + +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<p><span class="pagenum" id="Page_369">[Pg 369]</span></p> + +<h2 class="p4 nobreak" id="INDEX">INDEX</h2> +</div> + +<p>(The numbers, unless otherwise designated, refer to paragraphs.)</p> + + +<ul class="index"> +<li class="ifrst">Aborted, <a href="#p-220">220</a>, <a href="#p-291">291</a>.</li> + +<li class="indx">Absorption, <a href="#p-58">58</a>, <a href="#p-71">71</a>, <a href="#p-72">72</a>;</li> +<li class="isub1">Exp. <a href="#exp-39">39</a>.</li> +<li class="isub1">selective, <a href="#p-60">60</a>.</li> + +<li class="indx">Accessory buds, <a href="#p-158">158</a>.</li> + +<li class="indx">Accessory fruits, <a href="#p-302">302</a>.</li> + +<li class="indx">Adaptation, <a href="#p-206">206</a>, <a href="#p-237">237</a>.</li> + +<li class="indx">Adhesive fruits, <a href="#p-20">20</a>;</li> +<li class="isub1">Exp. <a href="#exp-20">20</a>.</li> + +<li class="indx">Adjustment of leaves, <a href="#p-196">196-202</a>.</li> + +<li class="indx">Adnate, <a href="#p-374">374</a>.</li> + +<li class="indx">Adventitious buds, <a href="#p-65">65</a>, <a href="#p-158">158</a>.</li> + +<li class="indx">Adventitious roots, <a href="#p-37">37</a>, <a href="#p-83">83</a>.</li> + +<li class="indx">Æcidium, <a href="#p-362">362</a>.</li> + +<li class="indx">Aëration, <a href="#p-319">319</a>.</li> + +<li class="indx">Aërial roots, <a href="#p-88">88</a>.</li> + +<li class="indx">Aggregate fruits, <a href="#p-301">301</a>, <a href="#p-303">303</a>.</li> + +<li class="indx">Air space, <a href="#p-114">114</a>, <a href="#p-116">116</a>, <a href="#p-184">184</a>.</li> + +<li class="indx">Akene, <a href="#p-234">234</a>, <a href="#p-296">296</a>, <a href="#p-302">302</a>, <a href="#p-305">305</a>.</li> + +<li class="indx">Albumin, <a href="#p-3">3</a>.</li> + +<li class="indx">Albuminous, <a href="#p-56">56</a>.</li> + +<li class="indx">Albuminous seed, <i>i.e.</i>, containing endosperm; Field work, p. <a href="#CH_I_FIELD">28</a>.</li> + +<li class="indx">Aleurone, <a href="#p-3">3</a>.</li> + +<li class="indx">Algæ, <a href="#p-333">333</a>, <a href="#p-336">336-342</a>.</li> + +<li class="indx">Alternate leaves, <a href="#p-168">168</a>.</li> + +<li class="indx">Alternation of generations, <a href="#p-395">395</a>, <a href="#p-400">400</a>, <a href="#p-409">409</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Analogous, <a href="#p-108">108</a>.</li> + +<li class="indx">Anatropous, Fig. <a href="#i_027a">26</a>.</li> + +<li class="indx">Angiosperms, <a href="#p-15">15</a>, <a href="#p-18">18</a>; Fig. <a href="#i_371">511</a>.</li> + +<li class="indx">Annuals, <a href="#p-91">91</a>.</li> + +<li class="indx">Annulus, <a href="#p-372">372</a>, <a href="#p-405">405</a>.</li> + +<li class="indx">Anther, <a href="#p-213">213</a>, <a href="#p-235">235</a>; Figs. <a href="#i_208">270-274</a>.</li> + +<li class="indx">Antheridia, <a href="#p-389">389</a>, <a href="#p-394">394</a>, <a href="#p-398">398</a>, <a href="#p-407">407</a>.</li> + +<li class="indx">Antheridial, <a href="#p-388">388</a>.</li> + +<li class="indx">Antherozoids, <a href="#p-389">389</a>, <a href="#p-392">392</a>, <a href="#p-395">395</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Antisepsis, <a href="#p-355">355</a>.</li> + +<li class="indx">Arch of the hypocotyl, <a href="#p-42">42</a>, <a href="#p-44">44</a>.</li> + +<li class="indx">Archegonia, <a href="#p-390">390</a>, <a href="#p-394">394</a>, <a href="#p-407">407</a>, <a href="#p-408">408</a>.</li> + +<li class="indx">Archegonial, <a href="#p-388">388</a>.</li> + +<li class="indx">Archegoniates, <a href="#p-408">408</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Archegonium, <a href="#p-391">391</a>, <a href="#p-394">394</a>, <a href="#p-398">398</a>.</li> + +<li class="indx">Asexual generation, <a href="#p-395">395</a>, <a href="#p-399">399</a>, <a href="#p-409">409</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Asexual reproduction, <a href="#p-394">394</a>, <a href="#p-395">395</a>.</li> + +<li class="indx">Asexual spore, <a href="#p-395">395</a>, <a href="#p-407">407</a>, <a href="#p-409">409</a>, <a href="#p-410">410</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Assurgent, <a href="#p-95">95</a>.</li> + +<li class="indx">Axial placenta, <a href="#p-216">216</a>, <a href="#p-300">300</a>.</li> + +<li class="indx">Axil, <a href="#p-100">100</a>, <a href="#p-166">166</a>.</li> + +<li class="indx">Axillary buds, <a href="#p-145">145</a>.</li> + +<li class="indx">Axis, <a href="#p-64">64</a>, <a href="#p-65">65</a>, <a href="#p-79">79</a>, <a href="#p-152">152</a>, <a href="#p-156">156</a>, <a href="#p-159">159</a>, + <a href="#p-161">161</a>.</li> + + +<li class="ifrst">Bacillus, <a href="#p-348">348</a>, <a href="#p-349">349</a>.</li> + +<li class="indx">Bacteria, <a href="#p-333">333</a>, <a href="#p-345">345</a>, <a href="#p-347">347-353</a>.</li> + +<li class="indx">Bark, <a href="#p-118">118</a>, <a href="#p-119">119</a>, <a href="#p-122">122</a>, p. <a href="#p-128">128</a>, (3).</li> + +<li class="indx">Basidia, <a href="#p-375">375</a>.</li> + +<li class="indx">Bast, <a href="#p-116">116</a>, <a href="#p-119">119</a>, <a href="#p-122">122</a>.</li> + +<li class="indx">Berry, <a href="#p-291">291</a>.</li> + +<li class="indx">Biennial, <a href="#p-92">92</a>.</li> + +<li class="indx">Bilabiate, <a href="#p-237">237</a>, <a href="#p-243">243</a>.</li> + +<li class="indx">Bilateral regularity, <a href="#p-219">219</a>.</li> + +<li class="indx">Bilateral zonation, <a href="#p-326">326</a>.</li> + +<li class="indx">Black rust, <a href="#p-360">360</a>.</li> + +<li class="indx">Blade of leaf, <a href="#p-165">165</a>.</li> + +<li class="indx">Biogenetic law, <a href="#p-253">253</a>.</li> + +<li class="indx">Biological factors, <a href="#p-309">309</a>.</li> + +<li class="indx">Bordered pits, <a href="#p-114">114</a>, <a href="#p-117">117</a>; Fig. <a href="#i_116a">123</a>.</li> + +<li class="indx">Boreal, <a href="#p-329">329</a>.</li> + +<li class="indx">Bract, <a href="#p-161">161</a>.</li> + +<li class="indx">Bryophytes, <a href="#p-334">334</a>, <a href="#p-385">385-401</a>.</li> + +<li class="indx">Bud scales, <a href="#p-147">147-149</a>.</li> + +<li class="indx">Buds, <a href="#p-145">145</a>, <a href="#p-155">155-158</a>.</li> + +<li class="indx">Bulb, <a href="#p-107">107</a>.</li> + +<li class="indx">Button (of mushroom), <a href="#p-370">370</a>.</li> + + +<li class="ifrst">Calyptra, <a href="#p-399">399</a>.</li> + +<li class="indx">Calyx, <a href="#p-211">211</a>.</li> + +<li class="indx">Cambium, <a href="#p-115">115</a>, <a href="#p-116">116</a>, <a href="#p-120">120</a>, <a href="#p-123">123</a>.</li> + +<li class="indx">Cap, <a href="#p-372">372</a>, <a href="#p-373">373</a>.</li> + +<li class="indx">Capillarity, <a href="#p-136">136</a>; Exp. <a href="#exp-53">53</a>.</li> + +<li class="indx">Capitate, <a href="#p-220">220</a>.</li> + +<li class="indx">Caprification, <a href="#p-279">279</a>, <a href="#p-305">305</a>.</li> + +<li class="indx">Caprifig, <a href="#p-279">279</a>.</li> + +<li class="indx">Capsule, <a href="#p-298">298</a>.</li> + +<li class="indx">Carbon, <a href="#p-27">27</a>, <a href="#p-28">28</a>, <a href="#p-62">62</a>.</li> + +<li class="indx">Carbon dioxide, <a href="#p-29">29</a>, <a href="#p-63">63</a>, <a href="#p-185">185</a>, <a href="#p-186">186</a>, <a href="#p-187">187</a>, <a href="#p-189">189</a>; + Exps. <a href="#exp-23">23</a>, <a href="#exp-25">25</a>.</li> + +<li class="indx">Carpels, <a href="#p-216">216</a>, <a href="#p-288">288</a>.</li> + +<li class="indx">Caruncle, <a href="#p-13">13</a>.</li> + +<li class="indx">Catkin, <a href="#p-161">161</a>.</li> + +<li class="indx">Caulicle, <a href="#p-46">46</a>.</li> + +<li class="indx">Cedar apples, Fig. <a href="#i_331">456</a>.</li> + +<li class="indx">Cell, <a href="#p-6">6</a>, <a href="#p-7">7</a>.</li> +<li class="isub1">collecting, <a href="#p-184">184</a>.</li> +<li class="isub1">companion, <a href="#p-114">114</a>.</li> + +<li class="indx">Cell sap, <a href="#p-7">7</a>, <a href="#p-110">110</a>.</li> + +<li class="indx">Cell wall, <a href="#p-7">7</a>, <a href="#p-183">183</a>.</li> + +<li class="indx">Central cylinder, <a href="#p-67">67</a>.</li> + +<li class="indx">Central placenta, <a href="#p-216">216</a>, <a href="#p-300">300</a>.</li> + +<li class="indx">Chalaza, <a href="#p-13">13</a>.</li> + +<li class="indx"><span class="pagenum" id="Page_370">[Pg 370]</span>Chlorophyll, <a href="#p-186">186</a>, <a href="#p-341">341</a>, <a href="#p-366">366</a>.</li> + +<li class="indx">Chlorophyll bodies, <a href="#p-184">184</a>, <a href="#p-186">186</a>, <a href="#p-382">382</a>.</li> + +<li class="indx">Cion, <a href="#p-65">65</a>.</li> + +<li class="indx">Classification, <a href="#p-90">90</a>, <a href="#p-252">252</a>, <a href="#p-283">283</a>, <a href="#p-343">343</a>, <a href="#p-384">384</a>, <a href="#p-411">411</a>, + <a href="#p-417">417</a>.</li> + +<li class="indx">Cleistogamic flowers, <a href="#p-272">272</a>.</li> + +<li class="indx">Climatic zones, <a href="#p-329">329</a>.</li> + +<li class="indx">Climbing stems, <a href="#p-96">96-98</a>.</li> + +<li class="indx">Clipped seed, p. <a href="#Page_12">12</a> (material).</li> + +<li class="indx">Closed bundle, <a href="#p-114">114</a>.</li> + +<li class="indx">Close-fertilized, <a href="#p-272">272</a>.</li> + +<li class="indx">Cluster cups, <a href="#p-362">362</a>.</li> + +<li class="indx">Coccus (pl. cocci), <a href="#p-339">339</a>, <a href="#p-348">348</a>.</li> + +<li class="indx">Coiled inflorescence, <a href="#p-162">162</a>.</li> + +<li class="indx">Collective fruits, <a href="#p-304">304</a>.</li> + +<li class="indx">Colony, <a href="#p-316">316</a>, <a href="#p-337">337</a>, <a href="#p-357">357</a>.</li> + +<li class="indx">Color of flowers, <a href="#p-276">276</a>.</li> + +<li class="indx">Compass plants, <a href="#p-199">199</a>.</li> + +<li class="indx">Complete flower, <a href="#p-219">219</a>.</li> + +<li class="indx">Composite, <a href="#p-235">235</a>, <a href="#p-381">381</a>.</li> + +<li class="indx">Composite flower, <a href="#p-236">236</a>.</li> + +<li class="indx">Compound leaf, <a href="#p-178">178</a>.</li> + +<li class="indx">Conduplicate, Figs. <a href="#i_149">159</a>, <a href="#i_149b">160</a>.</li> + +<li class="indx">Confluent, <a href="#p-404">404</a>.</li> + +<li class="indx">Conifers, <a href="#p-117">117</a>, <a href="#p-327">327</a>.</li> + +<li class="indx">Conjugation, <a href="#p-342">342</a>, <a href="#p-394">394</a>.</li> + +<li class="indx">Corolla, <a href="#p-211">211</a>.</li> + +<li class="indx">Cortex, <a href="#p-64">64</a>, <a href="#p-115">115</a>, <a href="#p-122">122</a>.</li> + +<li class="indx">Corymb, <a href="#p-161">161</a>.</li> + +<li class="indx">Cotyledon, <a href="#p-11">11</a>, <a href="#p-12">12</a>, <a href="#p-18">18</a>.</li> + +<li class="indx">Cross cut, <a href="#p-133">133</a>.</li> + +<li class="indx">Cross fertilization, <a href="#p-255">255</a>.</li> + +<li class="indx">Cross pollination, <a href="#p-255">255</a>.</li> + +<li class="indx">Crustaceous lichen, <a href="#p-384">384</a>.</li> + +<li class="indx">Cryptogam, <a href="#p-332">332</a>.</li> + +<li class="indx">Crystalloids, <a href="#p-60">60</a>.</li> + +<li class="indx">Culture medium, <a href="#p-347">347</a>; p. <a href="#p-306">306</a> (material).</li> + +<li class="indx">Cycle, <a href="#p-217">217</a>, <a href="#p-219">219</a>, <a href="#p-229">229</a>.</li> + +<li class="indx">Cycle of growth, <a href="#p-50">50</a>.</li> + +<li class="indx">Cyme, <a href="#p-162">162</a>.</li> + +<li class="indx">Cymose inflorescence, <a href="#p-162">162</a>.</li> + +<li class="indx">Cypress knees, <a href="#p-319">319</a>.</li> + + +<li class="ifrst">Deciduous, <a href="#p-203">203</a>.</li> + +<li class="indx">Declined, <a href="#p-95">95</a>.</li> + +<li class="indx">Decurrent, <a href="#p-374">374</a>.</li> + +<li class="indx">Definite annual growth, <a href="#p-153">153</a>.</li> + +<li class="indx">Definite inflorescence, <a href="#p-160">160</a>, <a href="#p-162">162</a>.</li> + +<li class="indx">Dehiscent fruits, <a href="#p-283">283</a>, <a href="#p-298">298</a>.</li> + +<li class="indx">Deliquescent, <a href="#p-144">144</a>.</li> + +<li class="indx">Determinate growth, <a href="#p-153">153</a>.</li> + +<li class="indx">Determinate inflorescence, <a href="#p-160">160</a>, <a href="#p-162">162</a>.</li> + +<li class="indx">Diadelphous, <a href="#p-239">239</a>.</li> + +<li class="indx">Diastase, <a href="#p-9">9</a>.</li> + +<li class="indx">Dichogamy, <a href="#p-269">269</a>.</li> + +<li class="indx">Dichotomous, <a href="#p-152">152</a>; Fig. <a href="#i_146">155</a>.</li> + +<li class="indx">Dicotyl, <a href="#p-42">42</a>, <a href="#p-115">115</a>, <a href="#p-116">116</a>, <a href="#p-171">171</a>, <a href="#p-220">220</a>.</li> + +<li class="indx">Dicotyledonous, <a href="#p-12">12</a>.</li> + +<li class="indx">Differentiate, <a href="#p-245">245</a>, <a href="#p-345">345</a>, <a href="#p-409">409</a>.</li> + +<li class="indx">Diffusion, <a href="#p-9">9</a>, <a href="#p-57">57</a>.</li> + +<li class="indx">Digestion, <a href="#p-9">9</a>.</li> + +<li class="indx">Dimorphic, <a href="#p-270">270</a>.</li> + +<li class="indx">Dimorphism, <a href="#p-270">270</a>.</li> + +<li class="indx">Dimorphous, <a href="#p-270">270</a>.</li> + +<li class="indx">Diœcious, <a href="#p-268">268</a>.</li> + +<li class="indx">Disinfection, <a href="#p-355">355</a>.</li> + +<li class="indx">Disk flower, <a href="#p-233">233</a>.</li> + +<li class="indx">Dispersal of seed, <a href="#p-19">19-25</a>.</li> + +<li class="indx">Dominant, <a href="#p-257">257</a>, <a href="#p-258">258</a>.</li> + +<li class="indx">Dormant buds, <a href="#p-157">157</a>.</li> + +<li class="indx">Dorsal; Figs. <a href="#i_273a">390</a>, <a href="#i_273b">391</a>.</li> + +<li class="indx">Drupe, <a href="#p-292">292</a>.</li> + +<li class="indx">Dry fruits, <a href="#p-283">283</a>, <a href="#p-293">293-300</a>.</li> + +<li class="indx">Duct, <a href="#p-67">67</a>, <a href="#p-111">111</a>, <a href="#p-114">114</a>.</li> + + +<li class="ifrst">Ecological factors, <a href="#p-310">310</a>.</li> + +<li class="indx">Ecology, <a href="#p-266">266</a>, <a href="#p-308">308</a>, <a href="#p-310">310</a>.</li> + +<li class="indx">Edgings, <a href="#p-134">134</a>.</li> + +<li class="indx">Egg cell, <a href="#p-251">251</a>, <a href="#p-391">391</a>.</li> + +<li class="indx">Elators, <a href="#p-393">393</a>.</li> + +<li class="indx">Embryo, <a href="#p-11">11</a>.</li> + +<li class="indx">Embryology, <a href="#p-253">253</a>.</li> + +<li class="indx">Embryo sac, <a href="#p-251">251</a>.</li> + +<li class="indx">Endodermis, <a href="#p-67">67</a> (b).</li> + +<li class="indx">Endosperm, <a href="#p-11">11</a>, <a href="#p-13">13</a>, <a href="#p-14">14</a>, <a href="#p-16">16</a>, <a href="#p-17">17</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Epicotyl, <a href="#p-45">45</a>, <a href="#p-46">46</a>, <a href="#p-47">47</a>.</li> + +<li class="indx">Epidermis, <a href="#p-64">64</a>, <a href="#p-115">115</a>, <a href="#p-122">122</a>, <a href="#p-183">183</a>.</li> + +<li class="indx">Epigynous, <a href="#p-225">225</a>, <a href="#p-230">230</a>.</li> + +<li class="indx">Epiphyte, <a href="#p-87">87</a>, <a href="#p-394">394</a>.</li> + +<li class="indx">Essential constituents, <a href="#p-62">62</a>.</li> + +<li class="indx">Essential organs, <a href="#p-212">212</a>.</li> + +<li class="indx">Evolution, <a href="#p-242">242</a>, <a href="#p-245">245</a>, <a href="#p-265">265</a>, <a href="#p-334">334</a>, <a href="#p-335">335</a>, <a href="#p-401">401</a>, + <a href="#p-414">414</a>, <a href="#p-415">415</a>, <a href="#p-417">417</a>, <a href="#p-418">418</a>, <a href="#p-419">419</a>.</li> + +<li class="indx">Evolutionary, <a href="#p-253">253</a>, <a href="#p-413">413</a>.</li> + +<li class="indx">Excentric attachment, <a href="#p-372">372</a>.</li> + +<li class="indx">Excurrent, <a href="#p-144">144</a>, <a href="#p-154">154</a>.</li> + + +<li class="ifrst">Factors, <a href="#p-54">54</a>, <a href="#p-265">265</a>, <a href="#p-310">310</a>.</li> + +<li class="indx">Fall of the leaf, <a href="#p-203">203</a>.</li> + +<li class="indx">Fascicled roots, <a href="#p-80">80</a>, <a href="#p-81">81</a>.</li> + +<li class="indx">Fats, <a href="#p-1">1</a>, <a href="#p-3">3</a>, <a href="#p-4">4</a>.</li> + +<li class="indx">Feather-veined, <a href="#p-172">172</a>.</li> + +<li class="indx">Ferments, <a href="#p-9">9</a>, <a href="#p-356">356</a>.</li> + +<li class="indx">Fertile, <a href="#p-404">404</a>.</li> + +<li class="indx">Fertile flower, <a href="#p-267">267</a>.</li> + +<li class="indx">Fertilization, <a href="#p-247">247</a>, <a href="#p-251">251</a>, <a href="#p-252">252</a>, <a href="#p-392">392</a>, <a href="#p-408">408</a>, + <a href="#p-416">416</a>.</li> + +<li class="indx">Fibrous roots, <a href="#p-37">37</a>, <a href="#p-78">78</a>, <a href="#p-80">80</a>, <a href="#p-81">81</a>.</li> + +<li class="indx">Fibrovascular bundle, <a href="#p-67">67</a>, <a href="#p-114">114</a>, <a href="#p-116">116</a>, <a href="#p-176">176</a>, <a href="#p-288">288</a>.</li> + +<li class="indx">Fig wasp, <a href="#p-279">279</a>.</li> + +<li class="indx">Filament of the stamen, <a href="#p-213">213</a>;</li> +<li class="isub1">a hairlike appendage, <a href="#p-341">341</a>, <a href="#p-361">361</a>, <a href="#p-369">369</a>, <a href="#p-393">393</a>, <a href="#p-396">396</a>.</li> + +<li class="indx">Filamentous algæ, <a href="#p-340">340</a>, <a href="#p-341">341</a>.</li> + +<li class="indx">Fission, <a href="#p-338">338</a>, <a href="#p-394">394</a>.</li> + +<li class="indx">Fleshy fruits, <a href="#p-283">283</a>, <a href="#p-288">288-292</a>.</li> + +<li class="indx">Floral envelopes, <a href="#p-211">211</a>.</li> + +<li class="indx">Foliaceous lichen, <a href="#p-379">379</a>, <a href="#p-384">384</a>.</li> + +<li class="indx">Follicle, <a href="#p-298">298</a>.</li> + +<li class="indx">Forestry, <a href="#p-139">139-142</a>.</li> + +<li class="indx">Forked stems, <a href="#p-152">152</a>.</li> + +<li class="indx">Formation, <a href="#p-316">316</a>.</li> + +<li class="indx">Free, <a href="#p-218">218</a>, <a href="#p-374">374</a>.</li> + +<li class="indx">Free central placenta, <a href="#p-216">216</a>.</li> + +<li class="indx">Free gills, <a href="#p-374">374</a>.</li> + +<li class="indx">Free ovary, <a href="#p-218">218</a>.</li> + +<li class="indx">Free veining, <a href="#p-402">402</a>.</li> + +<li class="indx">Freezing, <a href="#p-33">33</a>.</li> + +<li class="indx">Frog’s spit, <a href="#p-340">340</a>.</li> + +<li class="indx">Frond, <a href="#p-402">402</a>.</li> + +<li class="indx">Fruit, <a href="#p-282">282</a>.</li> + +<li class="indx">Fruticose lichen, <a href="#p-384">384</a>.</li> + +<li class="indx">Function, <a href="#p-41">41</a>.</li> + +<li class="indx">Fungi, <a href="#p-333">333</a>, <a href="#p-343">343</a>, <a href="#p-344">344</a>, <a href="#p-345">345</a>, <a href="#p-346">346</a>, + <a href="#p-378">378</a>.</li> + +<li class="indx">Fungus, <a href="#p-86">86</a>, <a href="#p-364">364</a>.</li> + + +<li class="ifrst">Gametes, <a href="#p-394">394</a>.</li> + +<li class="indx">Gametophyte, <a href="#p-394">394</a>, <a href="#p-395">395</a>, <a href="#p-396">396</a>, <a href="#p-406">406</a>, <a href="#p-407">407</a>, <a href="#p-410">410</a>, + <a href="#p-412">412</a>, <a href="#p-414">414</a>, <a href="#p-415">415</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Gemmæ, <a href="#p-387">387</a>.</li> + +<li class="indx">Generative cell, <a href="#p-249">249</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Geophilous, <a href="#p-321">321</a>.</li> + +<li class="indx">Geotropism, <a href="#p-51">51</a>, <a href="#p-52">52</a>, <a href="#p-53">53</a>.</li> + +<li class="indx">Germ, <a href="#p-2">2</a>, <a href="#p-11">11</a>.</li> + +<li class="indx">Germ cell, <a href="#p-251">251</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Germination, <a href="#p-32">32</a>, <a href="#p-35">35</a>; Exps. <a href="#exp-25">25</a>, <a href="#exp-26">26-29</a>.</li> + +<li class="indx">Germs, <a href="#p-352">352</a>, <a href="#p-355">355</a>.</li> + +<li class="indx">Gills (of mushroom), <a href="#p-374">374</a>.</li> + +<li class="indx">Girdling, <a href="#p-131">131</a>.</li> + +<li class="indx">Glutin, <a href="#p-3">3</a>.</li> + +<li class="indx">Gourd, <a href="#p-14">14</a>, <a href="#p-290">290</a>.</li> + +<li class="indx">Grain, <a href="#p-11">11</a>, <a href="#p-297">297</a>.</li> + +<li class="indx">Grain of timber, <a href="#p-133">133</a>, <a href="#p-134">134</a>, <a href="#p-135">135</a>.</li> + +<li class="indx">Gravity, <a href="#p-52">52</a>.</li> + +<li class="indx">Growth, <a href="#p-48">48-52</a>, <a href="#p-179">179</a>.</li> + +<li class="indx">Guard cell, <a href="#p-183">183</a>.</li> + +<li class="indx">Gymnosperms, <a href="#p-15">15</a>, <a href="#p-18">18</a>, <a href="#p-117">117</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Gymnosporangium, Fig. <a href="#i_331">456</a>.</li> + + +<li class="ifrst">Halophyte, <a href="#p-317">317</a>, <a href="#p-323">323</a>.</li> + +<li class="indx">Haustoria, <a href="#p-85">85</a>.</li> + +<li class="indx">Hay bacillus, <a href="#p-348">348</a>, <a href="#p-349">349</a>.</li> + +<li class="indx">Head, <a href="#p-161">161</a>.</li> + +<li class="indx">Heartwood, <a href="#p-131">131</a>.</li> + +<li class="indx">Heliotropic, <a href="#p-200">200</a>.</li> + +<li class="indx">Heliotropism, <a href="#p-198">198</a>.</li> + +<li class="indx">Herbaceous, <a href="#p-90">90</a>, <a href="#p-94">94</a>, <a href="#p-115">115</a>, <a href="#p-116">116</a>.</li> + +<li class="indx">Heredity, <a href="#p-264">264</a>, <a href="#p-265">265</a>.</li> + +<li class="indx">Hilum, <a href="#p-12">12</a>, <a href="#p-13">13</a>, <a href="#p-14">14</a>.</li> + +<li class="indx">Homologous, <a href="#p-108">108</a>.</li> + +<li class="indx">Host plant, <a href="#p-85">85</a>.</li> + +<li class="indx">Humus, <a href="#p-75">75</a>, <a href="#p-86">86</a>.</li> + +<li class="indx">Hybrid, <a href="#p-256">256</a>.</li> + +<li class="indx">Hybridization, <a href="#p-256">256</a>, <a href="#p-257">257</a>, <a href="#p-263">263</a>.</li> + +<li class="indx">Hydrophytes, <a href="#p-317">317</a>, <a href="#p-318">318</a>, <a href="#p-319">319</a>.</li> + +<li class="indx">Hymenium, <a href="#p-375">375</a>.</li> + +<li class="indx">Hymenomycetes, <a href="#p-375">375</a>.</li> + +<li class="indx"><span class="pagenum" id="Page_371">[Pg 371]</span>Hyphæ (sing. hypha), <a href="#p-369">369</a>, <a href="#p-380">380</a>.</li> + +<li class="indx">Hypocotyl, <a href="#p-11">11</a>, <a href="#p-12">12</a>, <a href="#p-14">14</a>, <a href="#p-46">46</a>.</li> +<li class="isub1">arched, <a href="#p-42">42</a>, <a href="#p-44">44</a>.</li> +<li class="isub1">straight, <a href="#p-44">44</a>.</li> + +<li class="indx">Hypogynous, <a href="#p-218">218</a>, <a href="#p-225">225</a>.</li> + + +<li class="ifrst">Imbibition, <a href="#p-136">136</a>.</li> + +<li class="indx">Imperfect flower, <a href="#p-219">219</a>, <a href="#p-231">231</a>, <a href="#p-267">267</a>.</li> + +<li class="indx">Impure hybrid, <a href="#p-258">258</a>, <a href="#p-259">259</a>.</li> + +<li class="indx">In-breeding, <a href="#p-254">254</a>.</li> + +<li class="indx">Incomplete flower, <a href="#p-219">219</a>.</li> + +<li class="indx">Incubation, <a href="#p-354">354</a>.</li> + +<li class="indx">Indefinite annual growth, <a href="#p-153">153</a>.</li> + +<li class="indx">Indefinite inflorescence, <a href="#p-160">160</a>, <a href="#p-161">161</a>.</li> + +<li class="indx">Indefinite number of parts, <a href="#p-229">229</a>.</li> + +<li class="indx">Indehiscent fruit, <a href="#p-283">283</a>, <a href="#p-294">294</a>.</li> + +<li class="indx">Indeterminate growth, <a href="#p-153">153</a>.</li> + +<li class="indx">Indeterminate inflorescence, <a href="#p-160">160</a>, <a href="#p-161">161</a>.</li> + +<li class="indx">Indusium, <a href="#p-404">404</a>.</li> + +<li class="indx">Inferior ovary, <a href="#p-221">221</a>, <a href="#p-225">225</a>.</li> + +<li class="indx">Inflorescence, <a href="#p-159">159</a>.</li> + +<li class="indx">Insectivorous plants, <a href="#p-208">208-210</a>.</li> + +<li class="indx">Internode, <a href="#p-46">46</a>, <a href="#p-110">110</a>; Exp. <a href="#exp-35">35</a>.</li> + +<li class="indx">Invasion, <a href="#p-328">328</a>.</li> + +<li class="indx">Inverted seed, <a href="#p-14">14</a>.</li> + +<li class="indx">Involucre, <a href="#p-161">161</a>, <a href="#p-232">232</a>.</li> + +<li class="indx">Involute, <a href="#p-373">373</a>; Fig. <a href="#i_195">251</a>.</li> + +<li class="indx">Iodine solution, Exp. <a href="#exp-3">3</a>.</li> + +<li class="indx">Irregular flower, <a href="#p-219">219</a>, <a href="#p-237">237</a>.</li> + +<li class="indx">Irritability, <a href="#p-201">201</a>.</li> + + +<li class="ifrst">Joint, <a href="#p-110">110</a>, <a href="#p-113">113</a>.</li> + + +<li class="ifrst">Keel, <a href="#p-238">238</a>.</li> + +<li class="indx">Knots, <a href="#p-137">137</a>.</li> + + +<li class="ifrst">Lamina, <a href="#p-209">209</a>.</li> + +<li class="indx">Laminæ, <a href="#p-368">368</a>, <a href="#p-374">374</a>.</li> + +<li class="indx">Lateral, <a href="#p-372">372</a>, <a href="#p-398">398</a>.</li> + +<li class="indx">Lateral buds, <a href="#p-145">145</a>.</li> + +<li class="indx">Leaf attachment, <a href="#p-167">167</a>.</li> + +<li class="indx">Leaf cups, <a href="#p-202">202</a>.</li> + +<li class="indx">Leaf scars, <a href="#p-146">146</a>.</li> + +<li class="indx">Leaf traces, <a href="#p-146">146</a>.</li> + +<li class="indx">Legume, <a href="#p-299">299</a>.</li> + +<li class="indx">Lenticels, <a href="#p-106">106</a>, <a href="#p-118">118</a>, <a href="#p-288">288</a>.</li> + +<li class="indx">Lichen, <a href="#p-379">379</a>.</li> + +<li class="indx">Life cycle, <a href="#p-359">359</a>, <a href="#p-364">364</a>.</li> + +<li class="indx">Loam, <a href="#p-75">75</a>.</li> + +<li class="indx">Lobing, <a href="#p-177">177</a>; Figs. <a href="#i_168_210">210-212</a>.</li> + +<li class="indx">Locule, <a href="#p-216">216</a>.</li> + +<li class="indx">Loment, Fig. <a href="#i_274">394</a>.</li> + +<li class="indx">Lyrate, Fig. <a href="#i_162a">197</a>.</li> + + +<li class="ifrst">Medulla, <a href="#p-119">119</a>, <a href="#p-122">122</a>.</li> + +<li class="indx">Medullary rays, <a href="#p-64">64</a>, <a href="#p-116">116</a>, <a href="#p-121">121</a>, <a href="#p-122">122</a>, <a href="#p-134">134</a>, + <a href="#p-135">135</a>.</li> + +<li class="indx">Megasporangia, <a href="#p-409">409</a>.</li> + +<li class="indx">Megaspore, <a href="#p-409">409</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Mendel’s law, <a href="#p-258">258</a>.</li> + +<li class="indx"><span class="pagenum" id="Page_372">[Pg 372]</span>Mesophyte, <a href="#p-317">317</a>, <a href="#p-324">324</a>.</li> + +<li class="indx">Metabolism, <a href="#p-193">193</a>.</li> + +<li class="indx">Microbe, <a href="#p-351">351</a>, <a href="#p-355">355</a>.</li> + +<li class="indx">Micrococcus, <a href="#p-339">339</a>.</li> + +<li class="indx">Micropyle, <a href="#p-12">12</a>, <a href="#p-13">13</a>, <a href="#p-14">14</a>, <a href="#p-15">15</a>, <a href="#p-45">45</a>.</li> + +<li class="indx">Microsporangia, <a href="#p-409">409</a>.</li> + +<li class="indx">Microspore, <a href="#p-409">409</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Midrib, <a href="#p-172">172</a>.</li> + +<li class="indx">Mixed forest, <a href="#p-139">139</a>, <a href="#p-324">324</a>.</li> + +<li class="indx">Modification, <a href="#p-100">100-108</a>, <a href="#p-206">206</a>, <a href="#p-207">207</a>, <a href="#p-289">289</a>.</li> + +<li class="indx">Molecule, <a href="#p-136">136</a>.</li> + +<li class="indx">Monadelphous, <a href="#p-239">239</a>.</li> + +<li class="indx">Monocotyl, <a href="#p-110">110</a>, <a href="#p-112">112</a>, <a href="#p-171">171</a>, <a href="#p-217">217</a>, <a href="#p-221">221</a>, + <a href="#p-418">418</a>.</li> + +<li class="indx">Monocotyledonous, <a href="#p-11">11</a>.</li> + +<li class="indx">Monœcious, <a href="#p-268">268</a>.</li> + +<li class="indx">Monopetalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Monosepalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Morphology, <a href="#p-108">108</a>.</li> +<li class="isub1">of the flower, <a href="#p-244">244</a>.</li> + +<li class="indx">Mosaic (leaf), <a href="#p-197">197</a>.</li> + +<li class="indx">Mosses, <a href="#p-334">334</a>, <a href="#p-396">396-401</a>.</li> + +<li class="indx">Muck, <a href="#p-75">75</a>.</li> + +<li class="indx">Multiple fruit, <a href="#p-304">304</a>, <a href="#p-305">305</a>.</li> + +<li class="indx">Mushroom, <a href="#p-333">333</a>, <a href="#p-367">367</a>.</li> + +<li class="indx">Mutation, <a href="#p-264">264</a>.</li> + +<li class="indx">Mycelium, <a href="#p-343">343</a>, <a href="#p-359">359</a>, <a href="#p-369">369</a>.</li> + +<li class="indx">Mychorrhiza, <a href="#p-86">86</a>.</li> + + +<li class="ifrst">Neck canal, <a href="#p-391">391</a>.</li> + +<li class="indx">Net-veined, <a href="#p-171">171</a>.</li> + +<li class="indx">Neuter, <a href="#p-267">267</a>.</li> + +<li class="indx">Neutral flower, <a href="#p-231">231</a>, <a href="#p-267">267</a>.</li> + +<li class="indx">Nitrogen, <a href="#p-62">62</a>, <a href="#p-63">63</a>, <a href="#p-188">188</a>.</li> + +<li class="indx">Nitrogenous food, <a href="#p-188">188</a>.</li> + +<li class="indx">Node, <a href="#p-46">46</a>, <a href="#p-65">65</a>, <a href="#p-110">110</a>, <a href="#p-113">113</a>.</li> + +<li class="indx">Nucleus, <a href="#p-7">7</a>, <a href="#p-341">341</a>.</li> + +<li class="indx">Numerical plan, <a href="#p-217">217</a>, <a href="#p-229">229</a>.</li> + +<li class="indx">Nut, <a href="#p-295">295</a>.</li> + +<li class="indx">Nutriment, <a href="#p-3">3</a>, <a href="#p-186">186</a>.</li> + +<li class="indx">Nutrition, <a href="#p-50">50</a>, <a href="#p-54">54</a>, <a href="#p-179">179</a>, <a href="#p-193">193</a>.</li> + +<li class="indx">Nyctitropic, <a href="#p-200">200</a>.</li> + + +<li class="ifrst">Obsolete, <a href="#p-220">220</a>.</li> + +<li class="indx">Oil, <a href="#p-1">1</a>, <a href="#p-3">3</a>, <a href="#p-8">8</a>.</li> + +<li class="indx">Oöspore, <a href="#p-393">393</a>, <a href="#p-394">394</a>, <a href="#p-395">395</a>.</li> + +<li class="indx">Open bundle, <a href="#p-116">116</a>.</li> + +<li class="indx">Operculum, <a href="#p-399">399</a>.</li> + +<li class="indx">Opposite leaves, <a href="#p-168">168</a>.</li> + +<li class="indx">Organ, <a href="#p-41">41</a>.</li> + +<li class="indx">Organic foods, <a href="#p-4">4</a>.</li> + +<li class="indx">Organs of reproduction, <a href="#p-40">40</a>.</li> +<li class="isub1">of vegetation, <a href="#p-40">40</a>.</li> + +<li class="indx">Osmosis, <a href="#p-56">56</a>, <a href="#p-57">57</a>.</li> + +<li class="indx">Ovary, <a href="#p-214">214</a>, <a href="#p-216">216</a>, <a href="#p-223">223</a>.</li> + +<li class="indx">Ovule, <a href="#p-216">216</a>.</li> + +<li class="indx">Oxidation, <a href="#p-27">27</a>; Exps. <a href="#exp-21">21</a>, <a href="#exp-22">22</a>.</li> + +<li class="indx">Oxygen, <a href="#p-62">62</a>, <a href="#p-63">63</a>, <a href="#p-186">186</a>, <a href="#p-187">187</a>; Exps. <a href="#exp-22">22</a>, <a href="#exp-66">66</a>.</li> + + +<li class="ifrst">Palisade cells, <a href="#p-184">184</a>.</li> + +<li class="indx">Palmate veining, <a href="#p-172">172</a>.</li> + +<li class="indx">Panicle, Fig. <a href="#i_153b">171</a>.</li> + +<li class="indx">Papilionaceous, <a href="#p-237">237</a>, <a href="#p-238">238</a>.</li> + +<li class="indx">Pappus, <a href="#p-234">234</a>.</li> + +<li class="indx">Parallel veining, <a href="#p-171">171</a>.</li> + +<li class="indx">Paraphyses, <a href="#p-375">375</a>, <a href="#p-398">398</a>.</li> + +<li class="indx">Parasitic, <a href="#p-5">5</a>, <a href="#p-345">345</a>, <a href="#p-364">364</a>.</li> + +<li class="indx">Parasitic plants, <a href="#p-85">85</a>, <a href="#p-343">343</a>, <a href="#p-382">382</a>.</li> + +<li class="indx">Parenchyma, <a href="#p-110">110</a>, <a href="#p-114">114</a>, <a href="#p-115">115</a>.</li> + +<li class="indx">Parietal, <a href="#p-216">216</a>.</li> + +<li class="indx">Pathogenic, <a href="#p-352">352</a>, <a href="#p-353">353</a>.</li> + +<li class="indx">Pedicel, <a href="#p-159">159</a>.</li> + +<li class="indx">Peduncle, <a href="#p-159">159</a>, <a href="#p-288">288</a>.</li> + +<li class="indx">Pentamerous, <a href="#p-229">229</a>.</li> + +<li class="indx">Pepo, <a href="#p-290">290</a>.</li> + +<li class="indx">Perennial, <a href="#p-93">93</a>.</li> + +<li class="indx">Perfect flower, <a href="#p-219">219</a>.</li> + +<li class="indx">Perianth, <a href="#p-211">211</a>.</li> + +<li class="indx">Pericarp, <a href="#p-288">288</a>.</li> + +<li class="indx">Perigynous, Figs. <a href="#i_219">301</a>, <a href="#i_219a">302</a>.</li> + +<li class="indx">Persistent, <a href="#p-166">166</a>.</li> + +<li class="indx">Petals, <a href="#p-211">211</a>.</li> + +<li class="indx">Petiole, <a href="#p-165">165</a>.</li> + +<li class="indx">Phanerogams, <a href="#p-331">331</a>, <a href="#p-332">332</a>.</li> + +<li class="indx">Phloem, <a href="#p-114">114</a>, <a href="#p-116">116</a>.</li> + +<li class="indx">Photosynthesis, <a href="#p-186">186</a>, <a href="#p-192">192</a>, <a href="#p-193">193</a>.</li> + +<li class="indx">Phototropism, <a href="#p-195">195</a>.</li> + +<li class="indx">Phyllotaxy, <a href="#p-168">168</a>, <a href="#p-169">169</a>.</li> + +<li class="indx">Pileus, <a href="#p-373">373</a>.</li> + +<li class="indx">Pinna, <a href="#p-402">402</a>.</li> + +<li class="indx">Pinnate veining, <a href="#p-172">172</a>.</li> + +<li class="indx">Pinnule, <a href="#p-402">402</a>.</li> + +<li class="indx">Pioneer plant, <a href="#p-316">316</a>, <a href="#p-319">319</a>, <a href="#p-320">320</a>.</li> + +<li class="indx">Pistil, <a href="#p-212">212</a>, <a href="#p-214">214</a>, <a href="#p-223">223</a>, <a href="#p-228">228</a>, <a href="#p-240">240</a>.</li> + +<li class="indx">Pistillate, <a href="#p-267">267</a>.</li> + +<li class="indx">Pitcher plant, <a href="#p-209">209</a>.</li> + +<li class="indx">Pith, <a href="#p-110">110</a>, <a href="#p-115">115</a>, <a href="#p-116">116</a>, <a href="#p-119">119</a>, <a href="#p-121">121</a>, + <a href="#p-122">122</a>.</li> + +<li class="indx">Pitted ducts, <a href="#p-114">114</a>.</li> + +<li class="indx">Placenta, <a href="#p-216">216</a>, <a href="#p-288">288</a>, <a href="#p-298">298</a>, <a href="#p-300">300</a>.</li> + +<li class="indx">Plant society, <a href="#p-316">316</a>.</li> + +<li class="indx">Plasmolysis, <a href="#p-59">59</a>.</li> + +<li class="indx">Pleurococcus, <a href="#p-337">337</a>.</li> + +<li class="indx">Plicate, <a href="#p-155">155</a>.</li> + +<li class="indx">Plumule, <a href="#p-11">11</a>, <a href="#p-12">12</a>, <a href="#p-14">14</a>, <a href="#p-45">45</a>, <a href="#p-46">46</a>.</li> + +<li class="indx">Pod, <a href="#p-298">298</a>.</li> + +<li class="indx">Pollen, <a href="#p-213">213</a>.</li> + +<li class="indx">Pollen grains, <a href="#p-213">213</a>.</li> + +<li class="indx">Pollen sac, <a href="#p-213">213</a>.</li> + +<li class="indx">Pollen tubes, <a href="#p-249">249</a>, <a href="#p-250">250</a>.</li> + +<li class="indx">Pollination, <a href="#p-215">215</a>, <a href="#p-247">247</a>.</li> + +<li class="indx">Polycotyledons, <a href="#p-15">15</a>, <a href="#p-45">45</a>.</li> + +<li class="indx">Polymorphic, <a href="#p-365">365</a>.</li> + +<li class="indx">Polymorphism, <a href="#p-365">365</a>.</li> + +<li class="indx">Polypetalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Polysepalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Pome, <a href="#p-288">288</a>.</li> + +<li class="indx">Prefoliation, <a href="#p-155">155</a>.</li> + +<li class="indx">Primary, <a href="#p-396">396</a>.</li> + +<li class="indx">Primary root, <a href="#p-42">42</a>, <a href="#p-79">79</a>.</li> + +<li class="indx">Pronuba, <a href="#p-278">278</a>.</li> + +<li class="indx">Prostate, <a href="#p-95">95</a>.</li> + +<li class="indx">Protection, <a href="#p-199">199</a>, <a href="#p-204">204</a>, <a href="#p-207">207</a>, <a href="#p-280">280</a>, <a href="#p-287">287</a>.</li> + +<li class="indx">Proteins, <a href="#p-3">3</a>, <a href="#p-8">8</a>, <a href="#p-33">33</a>, <a href="#p-188">188</a>, <a href="#p-204">204</a>.</li> + +<li class="indx">Prothallium, <a href="#p-407">407</a>.</li> + +<li class="indx">Protonema, <a href="#p-396">396</a>.</li> + +<li class="indx">Protoplasm, <a href="#p-6">6</a>, <a href="#p-7">7</a>, <a href="#p-57">57</a>, <a href="#p-58">58</a>, <a href="#p-67">67</a>, <a href="#p-110">110</a>, + <a href="#p-116">116</a>.</li> + +<li class="indx">Pteridophytes, <a href="#p-335">335</a>, <a href="#p-411">411</a>, <a href="#p-412">412</a>.</li> + +<li class="indx">Puccinia, <a href="#p-360">360</a>.</li> + +<li class="indx">Pure dominant, <a href="#p-258">258</a>, <a href="#p-259">259</a>.</li> + +<li class="indx">Pure forest, <a href="#p-139">139</a>, <a href="#p-324">324</a>.</li> + +<li class="indx">Pure recessive, <a href="#p-258">258</a>, <a href="#p-259">259</a>.</li> + +<li class="indx">Pycnidia, <a href="#p-363">363</a>.</li> + + +<li class="ifrst">Quartered cut, <a href="#p-135">135</a>.</li> + + +<li class="ifrst">Raceme, <a href="#p-161">161</a>.</li> + +<li class="indx">Rhachis, <a href="#p-178">178</a>.</li> + +<li class="indx">Radial section, <a href="#p-132">132</a>, <a href="#p-135">135</a>.</li> + +<li class="indx">Radicle, <a href="#p-46">46</a>.</li> + +<li class="indx">Rhaphe, <a href="#p-13">13</a>.</li> + +<li class="indx">Ray, <a href="#p-161">161</a>, <a href="#p-391">391</a>.</li> + +<li class="indx">Ray flowers, <a href="#p-231">231</a>.</li> + +<li class="indx">Receptacle, <a href="#p-211">211</a>, <a href="#p-288">288</a>, <a href="#p-289">289</a>, <a href="#p-388">388</a>, <a href="#p-390">390</a>, + <a href="#p-398">398</a>.</li> + +<li class="indx">Recessive, <a href="#p-257">257</a>, <a href="#p-258">258</a>.</li> + +<li class="indx">Red rust, <a href="#p-359">359</a>.</li> + +<li class="indx">Regular flower, <a href="#p-219">219</a>.</li> + +<li class="indx">Reproduction, <a href="#p-338">338</a>, <a href="#p-351">351</a>, <a href="#p-358">358</a>, <a href="#p-383">383</a>.</li> + +<li class="indx">Respiration, <a href="#p-30">30</a>, <a href="#p-31">31</a>, <a href="#p-191">191</a>, <a href="#p-192">192</a>.</li> + +<li class="indx">Resting spore, <a href="#p-338">338</a>, <a href="#p-342">342</a>, <a href="#p-358">358</a>, <a href="#p-394">394</a>.</li> + +<li class="indx">Reticulation, <a href="#p-172">172</a>, <a href="#p-402">402</a>.</li> + +<li class="indx">Retrogressive evolution, <a href="#p-418">418</a>.</li> + +<li class="indx">Revolute, <a href="#p-373">373</a>, <a href="#p-404">404</a>.</li> + +<li class="indx">Rhizoids, <a href="#p-379">379</a>, <a href="#p-386">386</a>.</li> + +<li class="indx">Rhizome, <a href="#p-105">105</a>.</li> + +<li class="indx">Ringing, <a href="#p-127">127</a>.</li> + +<li class="indx">Rings of growth, <a href="#p-122">122</a>, <a href="#p-123">123</a>, <a href="#p-134">134</a>, <a href="#p-135">135</a>.</li> + +<li class="indx">Rogue, <a href="#p-260">260</a>.</li> + +<li class="indx">Root cap, <a href="#p-39">39</a>.</li> + +<li class="indx">Root hairs, <a href="#p-38">38</a>, <a href="#p-67">67</a>.</li> + +<li class="indx">Root pressure, Exp. <a href="#exp-49">49</a>.</li> + +<li class="indx">Root pull, <a href="#p-69">69</a>.</li> + +<li class="indx">Rootstock, <a href="#p-105">105</a>.</li> + +<li class="indx">Root system, <a href="#p-89">89</a>.</li> + +<li class="indx">Root tubercles, <a href="#p-63">63</a>, <a href="#p-300">300</a>.</li> + +<li class="indx">Rosette, <a href="#p-197">197</a>.</li> + +<li class="indx">Rotation of crops, <a href="#p-24">24</a>, <a href="#p-327">327</a>.</li> + +<li class="indx">Runner, <a href="#p-95">95</a>.</li> + + +<li class="ifrst">Samara, <a href="#p-296">296</a>.</li> + +<li class="indx">Sap movement, <a href="#p-125">125</a>, <a href="#p-126">126</a>, <a href="#p-128">128</a>, <a href="#p-129">129</a>.</li> + +<li class="indx">Saprophyte, <a href="#p-86">86</a>.</li> + +<li class="indx">Sapwood, <a href="#p-131">131</a>.</li> + +<li class="indx">Scale leaves, <a href="#p-101">101</a>, <a href="#p-106">106</a>, <a href="#p-107">107</a>, <a href="#p-147">147-149</a>, <a href="#p-207">207</a>.</li> + +<li class="indx">Scape, <a href="#p-107">107</a>, <a href="#p-159">159</a>.</li> + +<li class="indx">Scorpioid inflorescence, <a href="#p-162">162</a>; Figs. <a href="#i_154">173-176</a>.</li> + +<li class="indx">Screenings, <a href="#p-20">20</a>; p. <a href="#Page_28">28</a>, Qn. 22.</li> + +<li class="indx">Secondary roots, <a href="#p-37">37</a>, <a href="#p-42">42</a>, <a href="#p-79">79</a>.</li> + +<li class="indx"><span class="pagenum" id="Page_373">[Pg 373]</span>Seed, <a href="#p-11">11-18</a>, <a href="#p-332">332</a>, <a href="#p-415">415</a>.</li> + +<li class="indx">Seed coat, <a href="#p-12">12</a>, <a href="#p-14">14</a>, <a href="#p-15">15</a>, <a href="#p-43">43</a>.</li> + +<li class="indx">Seedless fruits, <a href="#p-285">285</a>, <a href="#p-286">286</a>.</li> + +<li class="indx">Seedlings, <a href="#p-36">36</a>, <a href="#p-42">42</a>, <a href="#p-43">43</a>, <a href="#p-45">45</a>.</li> + +<li class="indx">Seed plants, <a href="#p-331">331</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Seed vessel, <a href="#p-282">282</a>.</li> + +<li class="indx">Selection, <a href="#p-260">260</a>, <a href="#p-265">265</a>, <a href="#p-286">286</a>.</li> +<li class="isub1">artificial, <a href="#p-262">262</a>.</li> +<li class="isub1">natural, <a href="#p-261">261</a>.</li> + +<li class="indx">Self-fertilization, <a href="#p-254">254</a>, <a href="#p-271">271</a>.</li> + +<li class="indx">Sepals, <a href="#p-211">211</a>.</li> + +<li class="indx">Sessile, <a href="#p-167">167</a>, <a href="#p-214">214</a>.</li> + +<li class="indx">Seta, <a href="#p-399">399</a>.</li> + +<li class="indx">Sexual generation, <a href="#p-395">395</a>, <a href="#p-396">396</a>, <a href="#p-406">406</a>, <a href="#p-410">410</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Sexual reproduction, <a href="#p-394">394</a>, <a href="#p-395">395</a>, <a href="#p-410">410</a>.</li> + +<li class="indx">Sheath, <a href="#p-67">67</a>, <a href="#p-116">116</a>.</li> + +<li class="indx">Shrinking of timber, <a href="#p-136">136</a>.</li> + +<li class="indx">Sieve tube, <a href="#p-114">114</a>.</li> + +<li class="indx">Slabs, <a href="#p-134">134</a>.</li> + +<li class="indx">Sleep movements, <a href="#p-200">200</a>.</li> + +<li class="indx">Soils, <a href="#p-75">75</a>, <a href="#p-77">77</a>.</li> + +<li class="indx">Sori, <a href="#p-404">404</a>.</li> + +<li class="indx">Spathe, <a href="#p-221">221</a>.</li> + +<li class="indx">Specialization, <a href="#p-237">237</a>.</li> + +<li class="indx">Spermatophytes, <a href="#p-331">331</a>, <a href="#p-335">335</a>, <a href="#p-394">394</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Spermatozoid, <a href="#p-389">389</a>.</li> + +<li class="indx">Spermogonia, <a href="#p-363">363</a>.</li> + +<li class="indx">Spike, <a href="#p-161">161</a>.</li> + +<li class="indx">Spirillum, <a href="#p-348">348</a>.</li> + +<li class="indx">Spirogyra, <a href="#p-341">341</a>.</li> + +<li class="indx">Sporangia, <a href="#p-390">390</a>, <a href="#p-405">405</a>.</li> + +<li class="indx">Spore, <a href="#p-332">332</a>, <a href="#p-349">349</a>, <a href="#p-350">350</a>, <a href="#p-377">377</a>, <a href="#p-406">406</a>, + <a href="#p-410">410</a>.</li> + +<li class="indx">Spore case, <a href="#p-390">390</a>, <a href="#p-393">393</a>, <a href="#p-405">405</a>.</li> + +<li class="indx">Spore print, <a href="#p-376">376</a>.</li> + +<li class="indx">Sporidium, <a href="#p-361">361</a>.</li> + +<li class="indx">Sporogonium, <a href="#p-393">393</a>, <a href="#p-399">399</a>.</li> + +<li class="indx">Sporophyll, <a href="#p-406">406</a>, <a href="#p-414">414</a>.</li> + +<li class="indx">Sporophyte, <a href="#p-393">393-395</a>, <a href="#p-399">399</a>, <a href="#p-406">406</a>, <a href="#p-410">410</a>, <a href="#p-412">412</a>, + <a href="#p-414">414</a>, <a href="#p-416">416</a>.</li> + +<li class="indx">Sport, <a href="#p-264">264</a>.</li> + +<li class="indx">Stamen, <a href="#p-212">212</a>, <a href="#p-213">213</a>.</li> + +<li class="indx">Staminate, <a href="#p-267">267</a>, <a href="#p-268">268</a>.</li> + +<li class="indx">Staminodia, <a href="#p-244">244</a>.</li> + +<li class="indx">Standard, <a href="#p-238">238</a>.</li> + +<li class="indx">Starch, <a href="#p-3">3</a>, <a href="#p-4">4</a>, <a href="#p-187">187</a>, <a href="#p-204">204</a>, <a href="#p-288">288</a>; + Exps. <a href="#exp-69">69</a>, <a href="#exp-70">70</a>.</li> + +<li class="indx">Stems, <a href="#p-90">90-99</a>.</li> + +<li class="indx">Sterile flower, <a href="#p-267">267</a>.</li> + +<li class="indx">Sterilization, <a href="#p-354">354</a>.</li> + +<li class="indx">Stigma, <a href="#p-214">214</a>.</li> + +<li class="indx">Stigmatic surface, <a href="#p-223">223</a>.</li> + +<li class="indx">Stimulus, <a href="#p-98">98</a>, <a href="#p-186">186</a>, <a href="#p-201">201</a>.</li> + +<li class="indx">Stipe, <a href="#p-240">240</a>, <a href="#p-372">372</a>, <a href="#p-402">402</a>.</li> + +<li class="indx">Stipule, <a href="#p-149">149</a>, <a href="#p-165">165</a>, <a href="#p-166">166</a>.</li> + +<li class="indx">Stolon, <a href="#p-95">95</a>.</li> + +<li class="indx">Stoma, <a href="#p-181">181</a>, <a href="#p-182">182</a>, <a href="#p-183">183</a>.</li> + +<li class="indx">Stomata, <a href="#p-181">181</a>, <a href="#p-182">182</a>.</li> + +<li class="indx">Stone fruit, <a href="#p-292">292</a>.</li> + +<li class="indx">Storage of food, <a href="#p-2">2</a>, <a href="#p-3">3</a>, <a href="#p-4">4</a>, <a href="#p-17">17</a>, <a href="#p-70">70</a>, <a href="#p-103">103</a>, + <a href="#p-104">104-107</a>, <a href="#p-287">287</a>.</li> + +<li class="indx"><span class="pagenum" id="Page_374">[Pg 374]</span>Strangling fig, <a href="#p-88">88</a>.</li> + +<li class="indx">Strobile, <a href="#p-411">411</a>.</li> + +<li class="indx">Strobiliaceous, <a href="#p-411">411</a>.</li> + +<li class="indx">Style, <a href="#p-214">214</a>.</li> + +<li class="indx">Succession, <a href="#p-327">327</a>.</li> + +<li class="indx">Sugars, <a href="#p-3">3</a>, <a href="#p-4">4</a>, <a href="#p-204">204</a>, <a href="#p-288">288</a>.</li> + +<li class="indx">Summer spores, <a href="#p-360">360</a>.</li> + +<li class="indx">Sundew, <a href="#p-210">210</a>.</li> + +<li class="indx">Superior ovary, <a href="#p-218">218</a>, <a href="#p-221">221</a>, <a href="#p-225">225</a>.</li> + +<li class="indx">Supernumerary buds, <a href="#p-158">158</a>.</li> + +<li class="indx">Suppressed, <a href="#p-220">220</a>.</li> + +<li class="indx">Survival of the fittest, <a href="#p-261">261</a>.</li> + +<li class="indx">Suture, <a href="#p-216">216</a>, <a href="#p-298">298</a>, <a href="#p-299">299</a>.</li> + +<li class="indx">Swarm spore, <a href="#p-349">349</a>.</li> + +<li class="indx">Swelling of timber, <a href="#p-136">136</a>.</li> + +<li class="indx">Symbiosis, <a href="#p-309">309</a>, <a href="#p-382">382</a>.</li> + +<li class="indx">Symmetrical flower, <a href="#p-219">219</a>.</li> + +<li class="indx">Sympetalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Syncarpous, <a href="#p-300">300</a>.</li> + +<li class="indx">Synsepalous, <a href="#p-211">211</a>.</li> + +<li class="indx">Systematic botany, <i>see</i> <a href="#APPENDIX">Appendix</a>.</li> + + +<li class="ifrst">Tangential cut, <a href="#p-132">132</a>, <a href="#p-134">134</a>.</li> + +<li class="indx">Tap root, <a href="#p-79">79</a>.</li> + +<li class="indx">Teleutospore, <a href="#p-360">360</a>.</li> + +<li class="indx">Tendril, <a href="#p-96">96</a>, <a href="#p-97">97</a>.</li> + +<li class="indx">Terminal bud, <a href="#p-145">145</a>, <a href="#p-154">154</a>.</li> + +<li class="indx">Testa, <a href="#p-14">14</a>.</li> + +<li class="indx">Thallophytes, <a href="#p-333">333</a>.</li> + +<li class="indx">Thallus, <a href="#p-333">333</a>, <a href="#p-341">341</a>, <a href="#p-343">343</a>, <a href="#p-379">379</a>, <a href="#p-380">380</a>, <a href="#p-381">381</a>, + <a href="#p-385">385</a>.</li> + +<li class="indx">Tillage, <a href="#p-76">76</a>.</li> + +<li class="indx">Tissue, <a href="#p-60">60</a>, <a href="#p-61">61</a>.</li> + +<li class="indx">Toadstools, <a href="#p-367">367</a>.</li> + +<li class="indx">Toxins, <a href="#p-345">345</a>.</li> + +<li class="indx">Tracheids, <a href="#p-114">114</a>, <a href="#p-117">117</a>.</li> + +<li class="indx">Trailing, <a href="#p-95">95</a>.</li> + +<li class="indx">Trama, <a href="#p-375">375</a>.</li> + +<li class="indx">Transpiration, <a href="#p-179">179</a>, <a href="#p-180">180</a>.</li> + +<li class="indx">Trifoliolate, Figs. <a href="#i_168_215">215</a>, <a href="#i_168_216">216</a>.</li> + +<li class="indx">Trimerous, <a href="#p-217">217</a>.</li> + +<li class="indx">Trimorphic, <a href="#p-270">270</a>.</li> + +<li class="indx">Tuber, <a href="#p-106">106</a>.</li> + +<li class="indx">Tumbleweeds, <a href="#p-23">23</a>.</li> + +<li class="indx">Turgidity, <a href="#p-7">7</a>.</li> + +<li class="indx">Turgor, <a href="#p-179">179</a>.</li> + +<li class="indx">Twining, cause of, <a href="#p-98">98</a>; Exp. <a href="#exp-55">55</a>.</li> + +<li class="indx">Twining stems, <a href="#p-96">96</a>; Exp. <a href="#exp-54">54</a>.</li> + +<li class="indx">Type, <a href="#p-18">18</a>, <a href="#p-260">260</a>, <a href="#p-263">263</a>, <a href="#p-265">265</a>, <a href="#p-336">336</a>, <a href="#p-411">411</a>.</li> + + +<li class="ifrst">Umbel, <a href="#p-161">161</a>.</li> + +<li class="indx">Umbonate, <a href="#p-373">373</a>.</li> + +<li class="indx">Underground stems, <a href="#p-104">104-107</a>.</li> + +<li class="indx">Unicellular, <a href="#p-337">337</a>.</li> + +<li class="indx">Unisexual, <a href="#p-267">267</a>.</li> + +<li class="indx">Uredo, <a href="#p-359">359</a>.</li> + +<li class="indx">Uredospore, <a href="#p-359">359</a>, <a href="#p-360">360</a>.</li> + + +<li class="ifrst">Variation, <a href="#p-263">263</a>, <a href="#p-264">264</a>, <a href="#p-265">265</a>.</li> + +<li class="indx">Vascular bundles, <a href="#p-111">111</a>.</li> + +<li class="indx">Vascular cryptogams, <a href="#p-403">403</a>, <a href="#p-411">411</a>, <a href="#p-412">412</a>.</li> + +<li class="indx">Vascular cylinder, <a href="#p-64">64</a>.</li> + +<li class="indx">Vascular system, <a href="#p-111">111</a>, <a href="#p-113">113</a>, <a href="#p-335">335</a>.</li> + +<li class="indx">Vegetative reproduction, <a href="#p-358">358</a>.</li> + +<li class="indx">Veil, <a href="#p-371">371</a>.</li> + +<li class="indx">Veins, <a href="#p-173">173-176</a>.</li> + +<li class="indx">Venter, <a href="#p-391">391</a>.</li> + +<li class="indx">Ventral, Figs. <a href="#i_273a">390</a>, <a href="#i_273b">391</a>.</li> + +<li class="indx">Vernation, <a href="#p-155">155</a>.</li> + +<li class="indx">Vessels, <a href="#p-111">111</a>.</li> + +<li class="indx">Vexillum, <a href="#p-238">238</a>, <a href="#p-239">239</a>.</li> + +<li class="indx">Vibrio, <a href="#p-348">348</a>.</li> + +<li class="indx">Vitality of seeds, <a href="#p-34">34</a>; Exp. <a href="#exp-30">30</a>.</li> + +<li class="indx">Volva, <a href="#p-371">371</a>.</li> + + +<li class="ifrst">Water roots, <a href="#p-39">39</a>, <a href="#p-84">84</a>.</li> + +<li class="indx">Whorled leaves, <a href="#p-168">168</a>.</li> + +<li class="indx">Wind pollination, <a href="#p-274">274</a>, <a href="#p-275">275</a>.</li> + +<li class="indx">Wings, <a href="#p-238">238</a>.</li> + +<li class="indx">Winter spores, <a href="#p-360">360</a>.</li> + + +<li class="ifrst">Xerophyte, <a href="#p-317">317</a>.</li> + +<li class="indx">Xerophyte societies, <a href="#p-317">317</a>, <a href="#p-320">320-322</a>.</li> + +<li class="indx">Xylem, <a href="#p-114">114</a>, <a href="#p-116">116</a>.</li> + + +<li class="ifrst">Yeast, <a href="#p-356">356</a>.</li> + +<li class="indx">Yeast colony, <a href="#p-357">357</a>.</li> + +<li class="indx">Yellow trumpets, <a href="#p-209">209</a>.</li> + +<li class="indx">Yucca, <a href="#p-278">278</a>.</li> + +<li class="indx">Yucca moth, <a href="#p-278">278</a>.</li> + + +<li class="ifrst">Zonation, <a href="#p-325">325</a>, <a href="#p-327">327</a>.</li> +<li class="isub1">bilateral, <a href="#p-326">326</a>.</li> +<li class="isub1">concentric, <a href="#p-326">326</a>.</li> +<li class="isub1">horizontal, <a href="#p-326">326</a>.</li> +<li class="isub1">vertical, <a href="#p-326">326</a>.</li> + +<li class="indx">Zones of vegetation, <a href="#p-325">325</a>.</li> +</ul> + + +<hr class="chap x-ebookmaker-drop"> + +<div class="chapter"> +<h2 class="nobreak" id="FOOTNOTES">FOOTNOTES:</h2> +</div> + +<div class="footnote"> + +<p><a id="Footnote_1" href="#FNanchor_1" class="label">[1]</a> Vines, “Lectures on the Physiology of Plants,” p. 282. See also Sachs, +“Physiology of Plants.”</p> + +</div> + +<div class="footnote"> + +<p><a id="Footnote_2" href="#FNanchor_2" class="label">[2]</a> Marshall Ward, “The Oak.”</p> + +</div> +<hr class="chap x-ebookmaker-drop"> + + +<div class="chapter transnote"> +<h2>TRANSCRIBER’S NOTE</h2> + +<p>Obvious typographical errors and punctuation errors have been +corrected after careful comparison with other occurrences within +the text and consultation of external sources.</p> + +<p>Some hyphens in words have been silently removed, some added, +when a predominant preference was found in the original book.</p> + +<p>Except for those changes noted below, all misspellings in the text, +and inconsistent or archaic usage, have been retained.</p> + +<table> +<tr> +<td class='tdr'><a href="#tn_45">p.  45</a>:</td> +<td class='tdl'>‘many of them has’</td> +<td class='tdl'>amended to ‘many of them have’</td> +</tr> +<tr> +<td class='tdr'><a href="#tn_281">p. 281</a>:</td> +<td class='tdl'> ‘are adpated’</td> +<td class='tdl'> amended to ‘are adapted’</td> +</tr> +<tr> +<td class='tdr'><a href="#tn_291">p. 291</a>:</td> +<td class='tdl'>‘and as it can, moveover’</td> +<td class='tdl'>amended to ‘and as it can, moreover’</td> +</tr> +<tr> +<td class='tdr'><a href="#tn_354">p. 354</a>:</td> +<td class='tdl'>‘eruption of Krakatao’</td> +<td class='tdl'>amended to ‘eruption of Krakatoa’</td> +</tr> +</table> +</div> + +<div style='text-align:center'>*** END OF THE PROJECT GUTENBERG EBOOK 78430 ***</div> +</body> +</html> diff --git a/78430-h/images/cover.jpg b/78430-h/images/cover.jpg Binary files differnew file mode 100755 index 0000000..e9edd64 --- /dev/null +++ b/78430-h/images/cover.jpg diff --git a/78430-h/images/fig_397.jpg b/78430-h/images/fig_397.jpg Binary files differnew file mode 100644 index 0000000..15f2a59 --- /dev/null +++ b/78430-h/images/fig_397.jpg diff --git a/78430-h/images/fig_398.jpg b/78430-h/images/fig_398.jpg Binary files differnew file mode 100644 index 0000000..51c7eff --- /dev/null +++ b/78430-h/images/fig_398.jpg diff --git a/78430-h/images/fig_399.jpg b/78430-h/images/fig_399.jpg Binary files differnew file mode 100644 index 0000000..9f605a6 --- /dev/null +++ b/78430-h/images/fig_399.jpg diff --git a/78430-h/images/i_001colophon.jpg b/78430-h/images/i_001colophon.jpg Binary files differnew file mode 100755 index 0000000..8576647 --- /dev/null +++ b/78430-h/images/i_001colophon.jpg diff --git a/78430-h/images/i_010.jpg b/78430-h/images/i_010.jpg Binary files differnew file mode 100755 index 0000000..a045607 --- /dev/null +++ b/78430-h/images/i_010.jpg diff --git a/78430-h/images/i_012.jpg b/78430-h/images/i_012.jpg Binary files differnew file mode 100755 index 0000000..c62fd65 --- /dev/null +++ b/78430-h/images/i_012.jpg diff --git a/78430-h/images/i_012a.jpg b/78430-h/images/i_012a.jpg Binary files differnew file mode 100755 index 0000000..394c68d --- /dev/null +++ b/78430-h/images/i_012a.jpg diff --git a/78430-h/images/i_013.jpg b/78430-h/images/i_013.jpg Binary files differnew file mode 100755 index 0000000..bf1b4ea --- /dev/null +++ b/78430-h/images/i_013.jpg diff --git a/78430-h/images/i_014.jpg b/78430-h/images/i_014.jpg Binary files differnew file mode 100755 index 0000000..4691d65 --- /dev/null +++ b/78430-h/images/i_014.jpg diff --git a/78430-h/images/i_015.jpg b/78430-h/images/i_015.jpg Binary files differnew file mode 100755 index 0000000..517f64f --- /dev/null +++ b/78430-h/images/i_015.jpg diff --git a/78430-h/images/i_017.jpg b/78430-h/images/i_017.jpg Binary files differnew file mode 100755 index 0000000..54dfa9f --- /dev/null +++ b/78430-h/images/i_017.jpg diff --git a/78430-h/images/i_018.jpg b/78430-h/images/i_018.jpg Binary files differnew file mode 100755 index 0000000..8f24b9e --- /dev/null +++ b/78430-h/images/i_018.jpg diff --git a/78430-h/images/i_021.jpg b/78430-h/images/i_021.jpg Binary files differnew file mode 100755 index 0000000..06bb380 --- /dev/null +++ b/78430-h/images/i_021.jpg diff --git a/78430-h/images/i_023.jpg b/78430-h/images/i_023.jpg Binary files differnew file mode 100755 index 0000000..868c893 --- /dev/null +++ b/78430-h/images/i_023.jpg diff --git a/78430-h/images/i_024.jpg b/78430-h/images/i_024.jpg Binary files differnew file mode 100755 index 0000000..d58737d --- /dev/null +++ b/78430-h/images/i_024.jpg diff --git a/78430-h/images/i_024a.jpg b/78430-h/images/i_024a.jpg Binary files differnew file mode 100644 index 0000000..92b3bce --- /dev/null +++ b/78430-h/images/i_024a.jpg diff --git a/78430-h/images/i_026.jpg b/78430-h/images/i_026.jpg Binary files differnew file mode 100755 index 0000000..ce1269d --- /dev/null +++ b/78430-h/images/i_026.jpg diff --git a/78430-h/images/i_027.jpg b/78430-h/images/i_027.jpg Binary files differnew file mode 100755 index 0000000..e565ab9 --- /dev/null +++ b/78430-h/images/i_027.jpg diff --git a/78430-h/images/i_027a.jpg b/78430-h/images/i_027a.jpg Binary files differnew file mode 100755 index 0000000..f0aa63e --- /dev/null +++ b/78430-h/images/i_027a.jpg diff --git a/78430-h/images/i_028.jpg b/78430-h/images/i_028.jpg Binary files differnew file mode 100755 index 0000000..54faeaa --- /dev/null +++ b/78430-h/images/i_028.jpg diff --git a/78430-h/images/i_029.jpg b/78430-h/images/i_029.jpg Binary files differnew file mode 100755 index 0000000..4e4859d --- /dev/null +++ b/78430-h/images/i_029.jpg diff --git a/78430-h/images/i_032.jpg b/78430-h/images/i_032.jpg Binary files differnew file mode 100755 index 0000000..25ab5fd --- /dev/null +++ b/78430-h/images/i_032.jpg diff --git a/78430-h/images/i_032a.jpg b/78430-h/images/i_032a.jpg Binary files differnew file mode 100755 index 0000000..ca705ec --- /dev/null +++ b/78430-h/images/i_032a.jpg diff --git a/78430-h/images/i_033b.jpg b/78430-h/images/i_033b.jpg Binary files differnew file mode 100755 index 0000000..6a91301 --- /dev/null +++ b/78430-h/images/i_033b.jpg diff --git a/78430-h/images/i_033xl.jpg b/78430-h/images/i_033xl.jpg Binary files differnew file mode 100644 index 0000000..068d0bf --- /dev/null +++ b/78430-h/images/i_033xl.jpg diff --git a/78430-h/images/i_033xr.jpg b/78430-h/images/i_033xr.jpg Binary files differnew file mode 100644 index 0000000..f36a8ab --- /dev/null +++ b/78430-h/images/i_033xr.jpg diff --git a/78430-h/images/i_034.jpg b/78430-h/images/i_034.jpg Binary files differnew file mode 100755 index 0000000..3188be6 --- /dev/null +++ b/78430-h/images/i_034.jpg diff --git a/78430-h/images/i_035_43.jpg b/78430-h/images/i_035_43.jpg Binary files differnew file mode 100644 index 0000000..395f2f0 --- /dev/null +++ b/78430-h/images/i_035_43.jpg diff --git a/78430-h/images/i_035_44.jpg b/78430-h/images/i_035_44.jpg Binary files differnew file mode 100644 index 0000000..05ce090 --- /dev/null +++ b/78430-h/images/i_035_44.jpg diff --git a/78430-h/images/i_036.jpg b/78430-h/images/i_036.jpg Binary files differnew file mode 100755 index 0000000..6563238 --- /dev/null +++ b/78430-h/images/i_036.jpg diff --git a/78430-h/images/i_040.jpg b/78430-h/images/i_040.jpg Binary files differnew file mode 100755 index 0000000..dc18e4f --- /dev/null +++ b/78430-h/images/i_040.jpg diff --git a/78430-h/images/i_045.jpg b/78430-h/images/i_045.jpg Binary files differnew file mode 100755 index 0000000..754d241 --- /dev/null +++ b/78430-h/images/i_045.jpg diff --git a/78430-h/images/i_046x.jpg b/78430-h/images/i_046x.jpg Binary files differnew file mode 100644 index 0000000..2f2548f --- /dev/null +++ b/78430-h/images/i_046x.jpg diff --git a/78430-h/images/i_047.jpg b/78430-h/images/i_047.jpg Binary files differnew file mode 100644 index 0000000..0a6cdab --- /dev/null +++ b/78430-h/images/i_047.jpg diff --git a/78430-h/images/i_047x.jpg b/78430-h/images/i_047x.jpg Binary files differnew file mode 100755 index 0000000..6c796e6 --- /dev/null +++ b/78430-h/images/i_047x.jpg diff --git a/78430-h/images/i_051.jpg b/78430-h/images/i_051.jpg Binary files differnew file mode 100755 index 0000000..68116e8 --- /dev/null +++ b/78430-h/images/i_051.jpg diff --git a/78430-h/images/i_052.jpg b/78430-h/images/i_052.jpg Binary files differnew file mode 100755 index 0000000..72267fc --- /dev/null +++ b/78430-h/images/i_052.jpg diff --git a/78430-h/images/i_052a.jpg b/78430-h/images/i_052a.jpg Binary files differnew file mode 100755 index 0000000..a008d84 --- /dev/null +++ b/78430-h/images/i_052a.jpg diff --git a/78430-h/images/i_053.jpg b/78430-h/images/i_053.jpg Binary files differnew file mode 100755 index 0000000..12a5467 --- /dev/null +++ b/78430-h/images/i_053.jpg diff --git a/78430-h/images/i_054.jpg b/78430-h/images/i_054.jpg Binary files differnew file mode 100755 index 0000000..40c56aa --- /dev/null +++ b/78430-h/images/i_054.jpg diff --git a/78430-h/images/i_055.jpg b/78430-h/images/i_055.jpg Binary files differnew file mode 100755 index 0000000..0afb1e4 --- /dev/null +++ b/78430-h/images/i_055.jpg diff --git a/78430-h/images/i_057.jpg b/78430-h/images/i_057.jpg Binary files differnew file mode 100755 index 0000000..ba01a3f --- /dev/null +++ b/78430-h/images/i_057.jpg diff --git a/78430-h/images/i_058.jpg b/78430-h/images/i_058.jpg Binary files differnew file mode 100755 index 0000000..7a1825c --- /dev/null +++ b/78430-h/images/i_058.jpg diff --git a/78430-h/images/i_058x.jpg b/78430-h/images/i_058x.jpg Binary files differnew file mode 100755 index 0000000..e7d673c --- /dev/null +++ b/78430-h/images/i_058x.jpg diff --git a/78430-h/images/i_059.jpg b/78430-h/images/i_059.jpg Binary files differnew file mode 100755 index 0000000..b29b20b --- /dev/null +++ b/78430-h/images/i_059.jpg diff --git a/78430-h/images/i_061.jpg b/78430-h/images/i_061.jpg Binary files differnew file mode 100755 index 0000000..76c3070 --- /dev/null +++ b/78430-h/images/i_061.jpg diff --git a/78430-h/images/i_063.jpg b/78430-h/images/i_063.jpg Binary files differnew file mode 100755 index 0000000..d1576ae --- /dev/null +++ b/78430-h/images/i_063.jpg diff --git a/78430-h/images/i_066.jpg b/78430-h/images/i_066.jpg Binary files differnew file mode 100755 index 0000000..c5e8e28 --- /dev/null +++ b/78430-h/images/i_066.jpg diff --git a/78430-h/images/i_067.jpg b/78430-h/images/i_067.jpg Binary files differnew file mode 100755 index 0000000..fa5b4c1 --- /dev/null +++ b/78430-h/images/i_067.jpg diff --git a/78430-h/images/i_069.jpg b/78430-h/images/i_069.jpg Binary files differnew file mode 100755 index 0000000..47d9e87 --- /dev/null +++ b/78430-h/images/i_069.jpg diff --git a/78430-h/images/i_070.jpg b/78430-h/images/i_070.jpg Binary files differnew file mode 100755 index 0000000..0c1565a --- /dev/null +++ b/78430-h/images/i_070.jpg diff --git a/78430-h/images/i_071.jpg b/78430-h/images/i_071.jpg Binary files differnew file mode 100755 index 0000000..fc5b5d0 --- /dev/null +++ b/78430-h/images/i_071.jpg diff --git a/78430-h/images/i_072.jpg b/78430-h/images/i_072.jpg Binary files differnew file mode 100755 index 0000000..7f0ef5d --- /dev/null +++ b/78430-h/images/i_072.jpg diff --git a/78430-h/images/i_072a.jpg b/78430-h/images/i_072a.jpg Binary files differnew file mode 100755 index 0000000..e87bfb3 --- /dev/null +++ b/78430-h/images/i_072a.jpg diff --git a/78430-h/images/i_073.jpg b/78430-h/images/i_073.jpg Binary files differnew file mode 100755 index 0000000..82f996e --- /dev/null +++ b/78430-h/images/i_073.jpg diff --git a/78430-h/images/i_074.jpg b/78430-h/images/i_074.jpg Binary files differnew file mode 100755 index 0000000..8945938 --- /dev/null +++ b/78430-h/images/i_074.jpg diff --git a/78430-h/images/i_077.jpg b/78430-h/images/i_077.jpg Binary files differnew file mode 100755 index 0000000..9455d91 --- /dev/null +++ b/78430-h/images/i_077.jpg diff --git a/78430-h/images/i_078.jpg b/78430-h/images/i_078.jpg Binary files differnew file mode 100755 index 0000000..0443f26 --- /dev/null +++ b/78430-h/images/i_078.jpg diff --git a/78430-h/images/i_079.jpg b/78430-h/images/i_079.jpg Binary files differnew file mode 100755 index 0000000..398ac0b --- /dev/null +++ b/78430-h/images/i_079.jpg diff --git a/78430-h/images/i_079a.jpg b/78430-h/images/i_079a.jpg Binary files differnew file mode 100755 index 0000000..15de30c --- /dev/null +++ b/78430-h/images/i_079a.jpg diff --git a/78430-h/images/i_080.jpg b/78430-h/images/i_080.jpg Binary files differnew file mode 100755 index 0000000..ea1c902 --- /dev/null +++ b/78430-h/images/i_080.jpg diff --git a/78430-h/images/i_083.jpg b/78430-h/images/i_083.jpg Binary files differnew file mode 100755 index 0000000..3642213 --- /dev/null +++ b/78430-h/images/i_083.jpg diff --git a/78430-h/images/i_084.jpg b/78430-h/images/i_084.jpg Binary files differnew file mode 100755 index 0000000..b2c027a --- /dev/null +++ b/78430-h/images/i_084.jpg diff --git a/78430-h/images/i_084a.jpg b/78430-h/images/i_084a.jpg Binary files differnew file mode 100755 index 0000000..eefb4f6 --- /dev/null +++ b/78430-h/images/i_084a.jpg diff --git a/78430-h/images/i_086.jpg b/78430-h/images/i_086.jpg Binary files differnew file mode 100755 index 0000000..bd023cc --- /dev/null +++ b/78430-h/images/i_086.jpg diff --git a/78430-h/images/i_086a.jpg b/78430-h/images/i_086a.jpg Binary files differnew file mode 100755 index 0000000..656c34c --- /dev/null +++ b/78430-h/images/i_086a.jpg diff --git a/78430-h/images/i_087.jpg b/78430-h/images/i_087.jpg Binary files differnew file mode 100755 index 0000000..25fa0d0 --- /dev/null +++ b/78430-h/images/i_087.jpg diff --git a/78430-h/images/i_088.jpg b/78430-h/images/i_088.jpg Binary files differnew file mode 100755 index 0000000..09c75e9 --- /dev/null +++ b/78430-h/images/i_088.jpg diff --git a/78430-h/images/i_092.jpg b/78430-h/images/i_092.jpg Binary files differnew file mode 100755 index 0000000..4e69a0b --- /dev/null +++ b/78430-h/images/i_092.jpg diff --git a/78430-h/images/i_093.jpg b/78430-h/images/i_093.jpg Binary files differnew file mode 100755 index 0000000..370e291 --- /dev/null +++ b/78430-h/images/i_093.jpg diff --git a/78430-h/images/i_094.jpg b/78430-h/images/i_094.jpg Binary files differnew file mode 100644 index 0000000..d410f96 --- /dev/null +++ b/78430-h/images/i_094.jpg diff --git a/78430-h/images/i_094_94.jpg b/78430-h/images/i_094_94.jpg Binary files differnew file mode 100644 index 0000000..538e587 --- /dev/null +++ b/78430-h/images/i_094_94.jpg diff --git a/78430-h/images/i_094_95.jpg b/78430-h/images/i_094_95.jpg Binary files differnew file mode 100644 index 0000000..a4fc467 --- /dev/null +++ b/78430-h/images/i_094_95.jpg diff --git a/78430-h/images/i_095.jpg b/78430-h/images/i_095.jpg Binary files differnew file mode 100755 index 0000000..7a9c790 --- /dev/null +++ b/78430-h/images/i_095.jpg diff --git a/78430-h/images/i_096.jpg b/78430-h/images/i_096.jpg Binary files differnew file mode 100755 index 0000000..db6dcfc --- /dev/null +++ b/78430-h/images/i_096.jpg diff --git a/78430-h/images/i_096a.jpg b/78430-h/images/i_096a.jpg Binary files differnew file mode 100644 index 0000000..09ee926 --- /dev/null +++ b/78430-h/images/i_096a.jpg diff --git a/78430-h/images/i_097.jpg b/78430-h/images/i_097.jpg Binary files differnew file mode 100755 index 0000000..b1264a3 --- /dev/null +++ b/78430-h/images/i_097.jpg diff --git a/78430-h/images/i_099.jpg b/78430-h/images/i_099.jpg Binary files differnew file mode 100755 index 0000000..64c46cd --- /dev/null +++ b/78430-h/images/i_099.jpg diff --git a/78430-h/images/i_100.jpg b/78430-h/images/i_100.jpg Binary files differnew file mode 100755 index 0000000..f8f289c --- /dev/null +++ b/78430-h/images/i_100.jpg diff --git a/78430-h/images/i_100a.jpg b/78430-h/images/i_100a.jpg Binary files differnew file mode 100755 index 0000000..10bc222 --- /dev/null +++ b/78430-h/images/i_100a.jpg diff --git a/78430-h/images/i_101.jpg b/78430-h/images/i_101.jpg Binary files differnew file mode 100755 index 0000000..0fa4adc --- /dev/null +++ b/78430-h/images/i_101.jpg diff --git a/78430-h/images/i_101a.jpg b/78430-h/images/i_101a.jpg Binary files differnew file mode 100755 index 0000000..730f553 --- /dev/null +++ b/78430-h/images/i_101a.jpg diff --git a/78430-h/images/i_102.jpg b/78430-h/images/i_102.jpg Binary files differnew file mode 100755 index 0000000..4e3e113 --- /dev/null +++ b/78430-h/images/i_102.jpg diff --git a/78430-h/images/i_102x.jpg b/78430-h/images/i_102x.jpg Binary files differnew file mode 100755 index 0000000..bdabbfa --- /dev/null +++ b/78430-h/images/i_102x.jpg diff --git a/78430-h/images/i_103x.jpg b/78430-h/images/i_103x.jpg Binary files differnew file mode 100755 index 0000000..b76536a --- /dev/null +++ b/78430-h/images/i_103x.jpg diff --git a/78430-h/images/i_104.jpg b/78430-h/images/i_104.jpg Binary files differnew file mode 100755 index 0000000..46ef140 --- /dev/null +++ b/78430-h/images/i_104.jpg diff --git a/78430-h/images/i_106.jpg b/78430-h/images/i_106.jpg Binary files differnew file mode 100755 index 0000000..aa78a13 --- /dev/null +++ b/78430-h/images/i_106.jpg diff --git a/78430-h/images/i_107.jpg b/78430-h/images/i_107.jpg Binary files differnew file mode 100755 index 0000000..b6c82ed --- /dev/null +++ b/78430-h/images/i_107.jpg diff --git a/78430-h/images/i_108.jpg b/78430-h/images/i_108.jpg Binary files differnew file mode 100755 index 0000000..d144a95 --- /dev/null +++ b/78430-h/images/i_108.jpg diff --git a/78430-h/images/i_109.jpg b/78430-h/images/i_109.jpg Binary files differnew file mode 100755 index 0000000..bbec4e9 --- /dev/null +++ b/78430-h/images/i_109.jpg diff --git a/78430-h/images/i_110.jpg b/78430-h/images/i_110.jpg Binary files differnew file mode 100755 index 0000000..a6b6680 --- /dev/null +++ b/78430-h/images/i_110.jpg diff --git a/78430-h/images/i_110a.jpg b/78430-h/images/i_110a.jpg Binary files differnew file mode 100755 index 0000000..d57ea3d --- /dev/null +++ b/78430-h/images/i_110a.jpg diff --git a/78430-h/images/i_111.jpg b/78430-h/images/i_111.jpg Binary files differnew file mode 100755 index 0000000..2ff76b5 --- /dev/null +++ b/78430-h/images/i_111.jpg diff --git a/78430-h/images/i_112.jpg b/78430-h/images/i_112.jpg Binary files differnew file mode 100755 index 0000000..3b60cf4 --- /dev/null +++ b/78430-h/images/i_112.jpg diff --git a/78430-h/images/i_113.jpg b/78430-h/images/i_113.jpg Binary files differnew file mode 100755 index 0000000..b669543 --- /dev/null +++ b/78430-h/images/i_113.jpg diff --git a/78430-h/images/i_114.jpg b/78430-h/images/i_114.jpg Binary files differnew file mode 100644 index 0000000..5b6652c --- /dev/null +++ b/78430-h/images/i_114.jpg diff --git a/78430-h/images/i_116.jpg b/78430-h/images/i_116.jpg Binary files differnew file mode 100755 index 0000000..fb37732 --- /dev/null +++ b/78430-h/images/i_116.jpg diff --git a/78430-h/images/i_116a.jpg b/78430-h/images/i_116a.jpg Binary files differnew file mode 100755 index 0000000..3eb6905 --- /dev/null +++ b/78430-h/images/i_116a.jpg diff --git a/78430-h/images/i_117.jpg b/78430-h/images/i_117.jpg Binary files differnew file mode 100755 index 0000000..7a229aa --- /dev/null +++ b/78430-h/images/i_117.jpg diff --git a/78430-h/images/i_118.jpg b/78430-h/images/i_118.jpg Binary files differnew file mode 100755 index 0000000..2aa47e4 --- /dev/null +++ b/78430-h/images/i_118.jpg diff --git a/78430-h/images/i_120.jpg b/78430-h/images/i_120.jpg Binary files differnew file mode 100755 index 0000000..3dbf8fc --- /dev/null +++ b/78430-h/images/i_120.jpg diff --git a/78430-h/images/i_121.jpg b/78430-h/images/i_121.jpg Binary files differnew file mode 100755 index 0000000..499e3ba --- /dev/null +++ b/78430-h/images/i_121.jpg diff --git a/78430-h/images/i_123.jpg b/78430-h/images/i_123.jpg Binary files differnew file mode 100755 index 0000000..5f015f2 --- /dev/null +++ b/78430-h/images/i_123.jpg diff --git a/78430-h/images/i_123a.jpg b/78430-h/images/i_123a.jpg Binary files differnew file mode 100755 index 0000000..a53c4df --- /dev/null +++ b/78430-h/images/i_123a.jpg diff --git a/78430-h/images/i_124.jpg b/78430-h/images/i_124.jpg Binary files differnew file mode 100755 index 0000000..ae582fc --- /dev/null +++ b/78430-h/images/i_124.jpg diff --git a/78430-h/images/i_125.jpg b/78430-h/images/i_125.jpg Binary files differnew file mode 100755 index 0000000..561a60d --- /dev/null +++ b/78430-h/images/i_125.jpg diff --git a/78430-h/images/i_127.jpg b/78430-h/images/i_127.jpg Binary files differnew file mode 100755 index 0000000..5f970ab --- /dev/null +++ b/78430-h/images/i_127.jpg diff --git a/78430-h/images/i_129.jpg b/78430-h/images/i_129.jpg Binary files differnew file mode 100755 index 0000000..dc52b20 --- /dev/null +++ b/78430-h/images/i_129.jpg diff --git a/78430-h/images/i_129a.jpg b/78430-h/images/i_129a.jpg Binary files differnew file mode 100755 index 0000000..038a920 --- /dev/null +++ b/78430-h/images/i_129a.jpg diff --git a/78430-h/images/i_130.jpg b/78430-h/images/i_130.jpg Binary files differnew file mode 100755 index 0000000..dc52655 --- /dev/null +++ b/78430-h/images/i_130.jpg diff --git a/78430-h/images/i_130a.jpg b/78430-h/images/i_130a.jpg Binary files differnew file mode 100644 index 0000000..e95f2c7 --- /dev/null +++ b/78430-h/images/i_130a.jpg diff --git a/78430-h/images/i_131.jpg b/78430-h/images/i_131.jpg Binary files differnew file mode 100755 index 0000000..894190a --- /dev/null +++ b/78430-h/images/i_131.jpg diff --git a/78430-h/images/i_131a.jpg b/78430-h/images/i_131a.jpg Binary files differnew file mode 100755 index 0000000..c4a2f2b --- /dev/null +++ b/78430-h/images/i_131a.jpg diff --git a/78430-h/images/i_132.jpg b/78430-h/images/i_132.jpg Binary files differnew file mode 100755 index 0000000..354cf76 --- /dev/null +++ b/78430-h/images/i_132.jpg diff --git a/78430-h/images/i_132a.jpg b/78430-h/images/i_132a.jpg Binary files differnew file mode 100755 index 0000000..3fb4e88 --- /dev/null +++ b/78430-h/images/i_132a.jpg diff --git a/78430-h/images/i_133.jpg b/78430-h/images/i_133.jpg Binary files differnew file mode 100755 index 0000000..37f25d4 --- /dev/null +++ b/78430-h/images/i_133.jpg diff --git a/78430-h/images/i_133a.jpg b/78430-h/images/i_133a.jpg Binary files differnew file mode 100755 index 0000000..2125c34 --- /dev/null +++ b/78430-h/images/i_133a.jpg diff --git a/78430-h/images/i_135.jpg b/78430-h/images/i_135.jpg Binary files differnew file mode 100755 index 0000000..04cd2e0 --- /dev/null +++ b/78430-h/images/i_135.jpg diff --git a/78430-h/images/i_136.jpg b/78430-h/images/i_136.jpg Binary files differnew file mode 100755 index 0000000..1f28dbf --- /dev/null +++ b/78430-h/images/i_136.jpg diff --git a/78430-h/images/i_136a.jpg b/78430-h/images/i_136a.jpg Binary files differnew file mode 100755 index 0000000..576abce --- /dev/null +++ b/78430-h/images/i_136a.jpg diff --git a/78430-h/images/i_140.jpg b/78430-h/images/i_140.jpg Binary files differnew file mode 100755 index 0000000..beb2111 --- /dev/null +++ b/78430-h/images/i_140.jpg diff --git a/78430-h/images/i_141.jpg b/78430-h/images/i_141.jpg Binary files differnew file mode 100755 index 0000000..4ae4ad6 --- /dev/null +++ b/78430-h/images/i_141.jpg diff --git a/78430-h/images/i_141a.jpg b/78430-h/images/i_141a.jpg Binary files differnew file mode 100755 index 0000000..e42ace6 --- /dev/null +++ b/78430-h/images/i_141a.jpg diff --git a/78430-h/images/i_142.jpg b/78430-h/images/i_142.jpg Binary files differnew file mode 100755 index 0000000..3a114bd --- /dev/null +++ b/78430-h/images/i_142.jpg diff --git a/78430-h/images/i_143.jpg b/78430-h/images/i_143.jpg Binary files differnew file mode 100755 index 0000000..922ad6a --- /dev/null +++ b/78430-h/images/i_143.jpg diff --git a/78430-h/images/i_143a.jpg b/78430-h/images/i_143a.jpg Binary files differnew file mode 100755 index 0000000..7e290bc --- /dev/null +++ b/78430-h/images/i_143a.jpg diff --git a/78430-h/images/i_144.jpg b/78430-h/images/i_144.jpg Binary files differnew file mode 100755 index 0000000..7c5a5d2 --- /dev/null +++ b/78430-h/images/i_144.jpg diff --git a/78430-h/images/i_145.jpg b/78430-h/images/i_145.jpg Binary files differnew file mode 100755 index 0000000..d9738dc --- /dev/null +++ b/78430-h/images/i_145.jpg diff --git a/78430-h/images/i_145a.jpg b/78430-h/images/i_145a.jpg Binary files differnew file mode 100755 index 0000000..78bc5cb --- /dev/null +++ b/78430-h/images/i_145a.jpg diff --git a/78430-h/images/i_146.jpg b/78430-h/images/i_146.jpg Binary files differnew file mode 100755 index 0000000..6b697dc --- /dev/null +++ b/78430-h/images/i_146.jpg diff --git a/78430-h/images/i_147.jpg b/78430-h/images/i_147.jpg Binary files differnew file mode 100755 index 0000000..5b1d988 --- /dev/null +++ b/78430-h/images/i_147.jpg diff --git a/78430-h/images/i_147a.jpg b/78430-h/images/i_147a.jpg Binary files differnew file mode 100755 index 0000000..7df9605 --- /dev/null +++ b/78430-h/images/i_147a.jpg diff --git a/78430-h/images/i_148.jpg b/78430-h/images/i_148.jpg Binary files differnew file mode 100755 index 0000000..37da397 --- /dev/null +++ b/78430-h/images/i_148.jpg diff --git a/78430-h/images/i_149.jpg b/78430-h/images/i_149.jpg Binary files differnew file mode 100755 index 0000000..d1f0e1e --- /dev/null +++ b/78430-h/images/i_149.jpg diff --git a/78430-h/images/i_149a.jpg b/78430-h/images/i_149a.jpg Binary files differnew file mode 100755 index 0000000..fc449bf --- /dev/null +++ b/78430-h/images/i_149a.jpg diff --git a/78430-h/images/i_149b.jpg b/78430-h/images/i_149b.jpg Binary files differnew file mode 100755 index 0000000..cd1eeaf --- /dev/null +++ b/78430-h/images/i_149b.jpg diff --git a/78430-h/images/i_149c.jpg b/78430-h/images/i_149c.jpg Binary files differnew file mode 100755 index 0000000..d519aa9 --- /dev/null +++ b/78430-h/images/i_149c.jpg diff --git a/78430-h/images/i_150.jpg b/78430-h/images/i_150.jpg Binary files differnew file mode 100755 index 0000000..ac55f53 --- /dev/null +++ b/78430-h/images/i_150.jpg diff --git a/78430-h/images/i_151.jpg b/78430-h/images/i_151.jpg Binary files differnew file mode 100755 index 0000000..5521c46 --- /dev/null +++ b/78430-h/images/i_151.jpg diff --git a/78430-h/images/i_151a.jpg b/78430-h/images/i_151a.jpg Binary files differnew file mode 100755 index 0000000..d945d49 --- /dev/null +++ b/78430-h/images/i_151a.jpg diff --git a/78430-h/images/i_152.jpg b/78430-h/images/i_152.jpg Binary files differnew file mode 100755 index 0000000..95fdbd9 --- /dev/null +++ b/78430-h/images/i_152.jpg diff --git a/78430-h/images/i_152a.jpg b/78430-h/images/i_152a.jpg Binary files differnew file mode 100755 index 0000000..6793cbc --- /dev/null +++ b/78430-h/images/i_152a.jpg diff --git a/78430-h/images/i_153.jpg b/78430-h/images/i_153.jpg Binary files differnew file mode 100755 index 0000000..85aeb65 --- /dev/null +++ b/78430-h/images/i_153.jpg diff --git a/78430-h/images/i_153a.jpg b/78430-h/images/i_153a.jpg Binary files differnew file mode 100755 index 0000000..625b908 --- /dev/null +++ b/78430-h/images/i_153a.jpg diff --git a/78430-h/images/i_153b.jpg b/78430-h/images/i_153b.jpg Binary files differnew file mode 100755 index 0000000..cc5defa --- /dev/null +++ b/78430-h/images/i_153b.jpg diff --git a/78430-h/images/i_153c.jpg b/78430-h/images/i_153c.jpg Binary files differnew file mode 100755 index 0000000..8c4beb7 --- /dev/null +++ b/78430-h/images/i_153c.jpg diff --git a/78430-h/images/i_154.jpg b/78430-h/images/i_154.jpg Binary files differnew file mode 100755 index 0000000..e09bb4a --- /dev/null +++ b/78430-h/images/i_154.jpg diff --git a/78430-h/images/i_154a.jpg b/78430-h/images/i_154a.jpg Binary files differnew file mode 100755 index 0000000..8b080ad --- /dev/null +++ b/78430-h/images/i_154a.jpg diff --git a/78430-h/images/i_157.jpg b/78430-h/images/i_157.jpg Binary files differnew file mode 100755 index 0000000..99d403d --- /dev/null +++ b/78430-h/images/i_157.jpg diff --git a/78430-h/images/i_157a.jpg b/78430-h/images/i_157a.jpg Binary files differnew file mode 100755 index 0000000..a97372e --- /dev/null +++ b/78430-h/images/i_157a.jpg diff --git a/78430-h/images/i_158a.jpg b/78430-h/images/i_158a.jpg Binary files differnew file mode 100644 index 0000000..5aca981 --- /dev/null +++ b/78430-h/images/i_158a.jpg diff --git a/78430-h/images/i_158b.jpg b/78430-h/images/i_158b.jpg Binary files differnew file mode 100644 index 0000000..eb1449a --- /dev/null +++ b/78430-h/images/i_158b.jpg diff --git a/78430-h/images/i_158c.jpg b/78430-h/images/i_158c.jpg Binary files differnew file mode 100644 index 0000000..323e317 --- /dev/null +++ b/78430-h/images/i_158c.jpg diff --git a/78430-h/images/i_159.jpg b/78430-h/images/i_159.jpg Binary files differnew file mode 100644 index 0000000..22e6f68 --- /dev/null +++ b/78430-h/images/i_159.jpg diff --git a/78430-h/images/i_160.jpg b/78430-h/images/i_160.jpg Binary files differnew file mode 100755 index 0000000..a8beee5 --- /dev/null +++ b/78430-h/images/i_160.jpg diff --git a/78430-h/images/i_160a.jpg b/78430-h/images/i_160a.jpg Binary files differnew file mode 100755 index 0000000..6027133 --- /dev/null +++ b/78430-h/images/i_160a.jpg diff --git a/78430-h/images/i_161.jpg b/78430-h/images/i_161.jpg Binary files differnew file mode 100755 index 0000000..b5e3f9f --- /dev/null +++ b/78430-h/images/i_161.jpg diff --git a/78430-h/images/i_162.jpg b/78430-h/images/i_162.jpg Binary files differnew file mode 100755 index 0000000..3e0246e --- /dev/null +++ b/78430-h/images/i_162.jpg diff --git a/78430-h/images/i_162a.jpg b/78430-h/images/i_162a.jpg Binary files differnew file mode 100755 index 0000000..c82d4b1 --- /dev/null +++ b/78430-h/images/i_162a.jpg diff --git a/78430-h/images/i_163.jpg b/78430-h/images/i_163.jpg Binary files differnew file mode 100755 index 0000000..7089605 --- /dev/null +++ b/78430-h/images/i_163.jpg diff --git a/78430-h/images/i_163a.jpg b/78430-h/images/i_163a.jpg Binary files differnew file mode 100755 index 0000000..4067a73 --- /dev/null +++ b/78430-h/images/i_163a.jpg diff --git a/78430-h/images/i_165.jpg b/78430-h/images/i_165.jpg Binary files differnew file mode 100755 index 0000000..b578c89 --- /dev/null +++ b/78430-h/images/i_165.jpg diff --git a/78430-h/images/i_165a.jpg b/78430-h/images/i_165a.jpg Binary files differnew file mode 100755 index 0000000..c805b7d --- /dev/null +++ b/78430-h/images/i_165a.jpg diff --git a/78430-h/images/i_165b.jpg b/78430-h/images/i_165b.jpg Binary files differnew file mode 100755 index 0000000..aeb7968 --- /dev/null +++ b/78430-h/images/i_165b.jpg diff --git a/78430-h/images/i_166.jpg b/78430-h/images/i_166.jpg Binary files differnew file mode 100755 index 0000000..c8a881c --- /dev/null +++ b/78430-h/images/i_166.jpg diff --git a/78430-h/images/i_166a.jpg b/78430-h/images/i_166a.jpg Binary files differnew file mode 100755 index 0000000..938db7f --- /dev/null +++ b/78430-h/images/i_166a.jpg diff --git a/78430-h/images/i_168_210.jpg b/78430-h/images/i_168_210.jpg Binary files differnew file mode 100644 index 0000000..7be3607 --- /dev/null +++ b/78430-h/images/i_168_210.jpg diff --git a/78430-h/images/i_168_211.jpg b/78430-h/images/i_168_211.jpg Binary files differnew file mode 100644 index 0000000..4a37295 --- /dev/null +++ b/78430-h/images/i_168_211.jpg diff --git a/78430-h/images/i_168_212.jpg b/78430-h/images/i_168_212.jpg Binary files differnew file mode 100644 index 0000000..9072525 --- /dev/null +++ b/78430-h/images/i_168_212.jpg diff --git a/78430-h/images/i_168_213.jpg b/78430-h/images/i_168_213.jpg Binary files differnew file mode 100644 index 0000000..bfb8a62 --- /dev/null +++ b/78430-h/images/i_168_213.jpg diff --git a/78430-h/images/i_168_214.jpg b/78430-h/images/i_168_214.jpg Binary files differnew file mode 100644 index 0000000..d9d3b1b --- /dev/null +++ b/78430-h/images/i_168_214.jpg diff --git a/78430-h/images/i_168_215.jpg b/78430-h/images/i_168_215.jpg Binary files differnew file mode 100644 index 0000000..c913ac5 --- /dev/null +++ b/78430-h/images/i_168_215.jpg diff --git a/78430-h/images/i_168_216.jpg b/78430-h/images/i_168_216.jpg Binary files differnew file mode 100644 index 0000000..e05368d --- /dev/null +++ b/78430-h/images/i_168_216.jpg diff --git a/78430-h/images/i_172.jpg b/78430-h/images/i_172.jpg Binary files differnew file mode 100755 index 0000000..6b719f1 --- /dev/null +++ b/78430-h/images/i_172.jpg diff --git a/78430-h/images/i_174.jpg b/78430-h/images/i_174.jpg Binary files differnew file mode 100755 index 0000000..7459128 --- /dev/null +++ b/78430-h/images/i_174.jpg diff --git a/78430-h/images/i_175.jpg b/78430-h/images/i_175.jpg Binary files differnew file mode 100755 index 0000000..68effb9 --- /dev/null +++ b/78430-h/images/i_175.jpg diff --git a/78430-h/images/i_175a.jpg b/78430-h/images/i_175a.jpg Binary files differnew file mode 100755 index 0000000..44e8f55 --- /dev/null +++ b/78430-h/images/i_175a.jpg diff --git a/78430-h/images/i_176.jpg b/78430-h/images/i_176.jpg Binary files differnew file mode 100755 index 0000000..9d1feac --- /dev/null +++ b/78430-h/images/i_176.jpg diff --git a/78430-h/images/i_177.jpg b/78430-h/images/i_177.jpg Binary files differnew file mode 100755 index 0000000..6a0b09a --- /dev/null +++ b/78430-h/images/i_177.jpg diff --git a/78430-h/images/i_177a.jpg b/78430-h/images/i_177a.jpg Binary files differnew file mode 100755 index 0000000..4251f8c --- /dev/null +++ b/78430-h/images/i_177a.jpg diff --git a/78430-h/images/i_179.jpg b/78430-h/images/i_179.jpg Binary files differnew file mode 100755 index 0000000..8d3d52e --- /dev/null +++ b/78430-h/images/i_179.jpg diff --git a/78430-h/images/i_179a.jpg b/78430-h/images/i_179a.jpg Binary files differnew file mode 100755 index 0000000..69953ae --- /dev/null +++ b/78430-h/images/i_179a.jpg diff --git a/78430-h/images/i_180.jpg b/78430-h/images/i_180.jpg Binary files differnew file mode 100755 index 0000000..07f57b5 --- /dev/null +++ b/78430-h/images/i_180.jpg diff --git a/78430-h/images/i_185.jpg b/78430-h/images/i_185.jpg Binary files differnew file mode 100755 index 0000000..473c589 --- /dev/null +++ b/78430-h/images/i_185.jpg diff --git a/78430-h/images/i_187.jpg b/78430-h/images/i_187.jpg Binary files differnew file mode 100755 index 0000000..917b867 --- /dev/null +++ b/78430-h/images/i_187.jpg diff --git a/78430-h/images/i_188.jpg b/78430-h/images/i_188.jpg Binary files differnew file mode 100755 index 0000000..dedd0e3 --- /dev/null +++ b/78430-h/images/i_188.jpg diff --git a/78430-h/images/i_189.jpg b/78430-h/images/i_189.jpg Binary files differnew file mode 100755 index 0000000..a499d84 --- /dev/null +++ b/78430-h/images/i_189.jpg diff --git a/78430-h/images/i_190.jpg b/78430-h/images/i_190.jpg Binary files differnew file mode 100755 index 0000000..ea3222f --- /dev/null +++ b/78430-h/images/i_190.jpg diff --git a/78430-h/images/i_190a.jpg b/78430-h/images/i_190a.jpg Binary files differnew file mode 100755 index 0000000..5271639 --- /dev/null +++ b/78430-h/images/i_190a.jpg diff --git a/78430-h/images/i_191.jpg b/78430-h/images/i_191.jpg Binary files differnew file mode 100755 index 0000000..0edbb92 --- /dev/null +++ b/78430-h/images/i_191.jpg diff --git a/78430-h/images/i_191a.jpg b/78430-h/images/i_191a.jpg Binary files differnew file mode 100755 index 0000000..6b6fbf7 --- /dev/null +++ b/78430-h/images/i_191a.jpg diff --git a/78430-h/images/i_191b.jpg b/78430-h/images/i_191b.jpg Binary files differnew file mode 100755 index 0000000..332a6a4 --- /dev/null +++ b/78430-h/images/i_191b.jpg diff --git a/78430-h/images/i_192.jpg b/78430-h/images/i_192.jpg Binary files differnew file mode 100755 index 0000000..2d2d61e --- /dev/null +++ b/78430-h/images/i_192.jpg diff --git a/78430-h/images/i_193.jpg b/78430-h/images/i_193.jpg Binary files differnew file mode 100755 index 0000000..8cbd914 --- /dev/null +++ b/78430-h/images/i_193.jpg diff --git a/78430-h/images/i_193a.jpg b/78430-h/images/i_193a.jpg Binary files differnew file mode 100755 index 0000000..0dd9444 --- /dev/null +++ b/78430-h/images/i_193a.jpg diff --git a/78430-h/images/i_195.jpg b/78430-h/images/i_195.jpg Binary files differnew file mode 100755 index 0000000..9f07b09 --- /dev/null +++ b/78430-h/images/i_195.jpg diff --git a/78430-h/images/i_195_252.jpg b/78430-h/images/i_195_252.jpg Binary files differnew file mode 100644 index 0000000..586edf1 --- /dev/null +++ b/78430-h/images/i_195_252.jpg diff --git a/78430-h/images/i_195_253.jpg b/78430-h/images/i_195_253.jpg Binary files differnew file mode 100644 index 0000000..1865d5c --- /dev/null +++ b/78430-h/images/i_195_253.jpg diff --git a/78430-h/images/i_196.jpg b/78430-h/images/i_196.jpg Binary files differnew file mode 100755 index 0000000..e4f9489 --- /dev/null +++ b/78430-h/images/i_196.jpg diff --git a/78430-h/images/i_200.jpg b/78430-h/images/i_200.jpg Binary files differnew file mode 100755 index 0000000..e75624a --- /dev/null +++ b/78430-h/images/i_200.jpg diff --git a/78430-h/images/i_200a.jpg b/78430-h/images/i_200a.jpg Binary files differnew file mode 100755 index 0000000..109662c --- /dev/null +++ b/78430-h/images/i_200a.jpg diff --git a/78430-h/images/i_201.jpg b/78430-h/images/i_201.jpg Binary files differnew file mode 100755 index 0000000..dc5ad96 --- /dev/null +++ b/78430-h/images/i_201.jpg diff --git a/78430-h/images/i_202.jpg b/78430-h/images/i_202.jpg Binary files differnew file mode 100755 index 0000000..aa22d0e --- /dev/null +++ b/78430-h/images/i_202.jpg diff --git a/78430-h/images/i_202a.jpg b/78430-h/images/i_202a.jpg Binary files differnew file mode 100755 index 0000000..e3b7858 --- /dev/null +++ b/78430-h/images/i_202a.jpg diff --git a/78430-h/images/i_203.jpg b/78430-h/images/i_203.jpg Binary files differnew file mode 100755 index 0000000..d67510a --- /dev/null +++ b/78430-h/images/i_203.jpg diff --git a/78430-h/images/i_207.jpg b/78430-h/images/i_207.jpg Binary files differnew file mode 100755 index 0000000..ae4ff30 --- /dev/null +++ b/78430-h/images/i_207.jpg diff --git a/78430-h/images/i_207a.jpg b/78430-h/images/i_207a.jpg Binary files differnew file mode 100755 index 0000000..dd55f6c --- /dev/null +++ b/78430-h/images/i_207a.jpg diff --git a/78430-h/images/i_208.jpg b/78430-h/images/i_208.jpg Binary files differnew file mode 100755 index 0000000..23163b3 --- /dev/null +++ b/78430-h/images/i_208.jpg diff --git a/78430-h/images/i_209.jpg b/78430-h/images/i_209.jpg Binary files differnew file mode 100755 index 0000000..9be3ea6 --- /dev/null +++ b/78430-h/images/i_209.jpg diff --git a/78430-h/images/i_210.jpg b/78430-h/images/i_210.jpg Binary files differnew file mode 100755 index 0000000..fa599ad --- /dev/null +++ b/78430-h/images/i_210.jpg diff --git a/78430-h/images/i_211.jpg b/78430-h/images/i_211.jpg Binary files differnew file mode 100755 index 0000000..4455124 --- /dev/null +++ b/78430-h/images/i_211.jpg diff --git a/78430-h/images/i_211a.jpg b/78430-h/images/i_211a.jpg Binary files differnew file mode 100755 index 0000000..f9798a8 --- /dev/null +++ b/78430-h/images/i_211a.jpg diff --git a/78430-h/images/i_213.jpg b/78430-h/images/i_213.jpg Binary files differnew file mode 100755 index 0000000..815f6e6 --- /dev/null +++ b/78430-h/images/i_213.jpg diff --git a/78430-h/images/i_214.jpg b/78430-h/images/i_214.jpg Binary files differnew file mode 100755 index 0000000..0ba7168 --- /dev/null +++ b/78430-h/images/i_214.jpg diff --git a/78430-h/images/i_215.jpg b/78430-h/images/i_215.jpg Binary files differnew file mode 100755 index 0000000..d6d7d22 --- /dev/null +++ b/78430-h/images/i_215.jpg diff --git a/78430-h/images/i_215a.jpg b/78430-h/images/i_215a.jpg Binary files differnew file mode 100755 index 0000000..4be0fcf --- /dev/null +++ b/78430-h/images/i_215a.jpg diff --git a/78430-h/images/i_215b.jpg b/78430-h/images/i_215b.jpg Binary files differnew file mode 100755 index 0000000..2a6fcbe --- /dev/null +++ b/78430-h/images/i_215b.jpg diff --git a/78430-h/images/i_215c.jpg b/78430-h/images/i_215c.jpg Binary files differnew file mode 100755 index 0000000..d218a3f --- /dev/null +++ b/78430-h/images/i_215c.jpg diff --git a/78430-h/images/i_216.jpg b/78430-h/images/i_216.jpg Binary files differnew file mode 100755 index 0000000..7ad579e --- /dev/null +++ b/78430-h/images/i_216.jpg diff --git a/78430-h/images/i_217.jpg b/78430-h/images/i_217.jpg Binary files differnew file mode 100755 index 0000000..def3556 --- /dev/null +++ b/78430-h/images/i_217.jpg diff --git a/78430-h/images/i_218.jpg b/78430-h/images/i_218.jpg Binary files differnew file mode 100755 index 0000000..bca0787 --- /dev/null +++ b/78430-h/images/i_218.jpg diff --git a/78430-h/images/i_219.jpg b/78430-h/images/i_219.jpg Binary files differnew file mode 100755 index 0000000..0e9ba0f --- /dev/null +++ b/78430-h/images/i_219.jpg diff --git a/78430-h/images/i_219a.jpg b/78430-h/images/i_219a.jpg Binary files differnew file mode 100755 index 0000000..e93b08a --- /dev/null +++ b/78430-h/images/i_219a.jpg diff --git a/78430-h/images/i_220.jpg b/78430-h/images/i_220.jpg Binary files differnew file mode 100644 index 0000000..96d4c76 --- /dev/null +++ b/78430-h/images/i_220.jpg diff --git a/78430-h/images/i_222.jpg b/78430-h/images/i_222.jpg Binary files differnew file mode 100755 index 0000000..bc14f02 --- /dev/null +++ b/78430-h/images/i_222.jpg diff --git a/78430-h/images/i_223.jpg b/78430-h/images/i_223.jpg Binary files differnew file mode 100755 index 0000000..8dcd5a7 --- /dev/null +++ b/78430-h/images/i_223.jpg diff --git a/78430-h/images/i_225.jpg b/78430-h/images/i_225.jpg Binary files differnew file mode 100755 index 0000000..3964cb4 --- /dev/null +++ b/78430-h/images/i_225.jpg diff --git a/78430-h/images/i_227.jpg b/78430-h/images/i_227.jpg Binary files differnew file mode 100755 index 0000000..bd346d9 --- /dev/null +++ b/78430-h/images/i_227.jpg diff --git a/78430-h/images/i_227a.jpg b/78430-h/images/i_227a.jpg Binary files differnew file mode 100755 index 0000000..f87b0ac --- /dev/null +++ b/78430-h/images/i_227a.jpg diff --git a/78430-h/images/i_228.jpg b/78430-h/images/i_228.jpg Binary files differnew file mode 100755 index 0000000..a2019e3 --- /dev/null +++ b/78430-h/images/i_228.jpg diff --git a/78430-h/images/i_228a.jpg b/78430-h/images/i_228a.jpg Binary files differnew file mode 100755 index 0000000..bcbdc6f --- /dev/null +++ b/78430-h/images/i_228a.jpg diff --git a/78430-h/images/i_231.jpg b/78430-h/images/i_231.jpg Binary files differnew file mode 100755 index 0000000..6f4c913 --- /dev/null +++ b/78430-h/images/i_231.jpg diff --git a/78430-h/images/i_232.jpg b/78430-h/images/i_232.jpg Binary files differnew file mode 100755 index 0000000..b636da4 --- /dev/null +++ b/78430-h/images/i_232.jpg diff --git a/78430-h/images/i_234.jpg b/78430-h/images/i_234.jpg Binary files differnew file mode 100755 index 0000000..e4c8f51 --- /dev/null +++ b/78430-h/images/i_234.jpg diff --git a/78430-h/images/i_234a.jpg b/78430-h/images/i_234a.jpg Binary files differnew file mode 100755 index 0000000..126bec1 --- /dev/null +++ b/78430-h/images/i_234a.jpg diff --git a/78430-h/images/i_235.jpg b/78430-h/images/i_235.jpg Binary files differnew file mode 100755 index 0000000..55fca40 --- /dev/null +++ b/78430-h/images/i_235.jpg diff --git a/78430-h/images/i_237.jpg b/78430-h/images/i_237.jpg Binary files differnew file mode 100755 index 0000000..c5654ed --- /dev/null +++ b/78430-h/images/i_237.jpg diff --git a/78430-h/images/i_238.jpg b/78430-h/images/i_238.jpg Binary files differnew file mode 100755 index 0000000..7fdee23 --- /dev/null +++ b/78430-h/images/i_238.jpg diff --git a/78430-h/images/i_238a.jpg b/78430-h/images/i_238a.jpg Binary files differnew file mode 100755 index 0000000..0227a74 --- /dev/null +++ b/78430-h/images/i_238a.jpg diff --git a/78430-h/images/i_241.jpg b/78430-h/images/i_241.jpg Binary files differnew file mode 100755 index 0000000..2179a74 --- /dev/null +++ b/78430-h/images/i_241.jpg diff --git a/78430-h/images/i_242.jpg b/78430-h/images/i_242.jpg Binary files differnew file mode 100755 index 0000000..c4cef7b --- /dev/null +++ b/78430-h/images/i_242.jpg diff --git a/78430-h/images/i_243.jpg b/78430-h/images/i_243.jpg Binary files differnew file mode 100755 index 0000000..c89aaf3 --- /dev/null +++ b/78430-h/images/i_243.jpg diff --git a/78430-h/images/i_246.jpg b/78430-h/images/i_246.jpg Binary files differnew file mode 100755 index 0000000..4b08a13 --- /dev/null +++ b/78430-h/images/i_246.jpg diff --git a/78430-h/images/i_246a.jpg b/78430-h/images/i_246a.jpg Binary files differnew file mode 100755 index 0000000..7d739d3 --- /dev/null +++ b/78430-h/images/i_246a.jpg diff --git a/78430-h/images/i_247.jpg b/78430-h/images/i_247.jpg Binary files differnew file mode 100755 index 0000000..90a25e6 --- /dev/null +++ b/78430-h/images/i_247.jpg diff --git a/78430-h/images/i_247a.jpg b/78430-h/images/i_247a.jpg Binary files differnew file mode 100755 index 0000000..2e85b87 --- /dev/null +++ b/78430-h/images/i_247a.jpg diff --git a/78430-h/images/i_248.jpg b/78430-h/images/i_248.jpg Binary files differnew file mode 100755 index 0000000..1d411a9 --- /dev/null +++ b/78430-h/images/i_248.jpg diff --git a/78430-h/images/i_250.jpg b/78430-h/images/i_250.jpg Binary files differnew file mode 100755 index 0000000..5392fad --- /dev/null +++ b/78430-h/images/i_250.jpg diff --git a/78430-h/images/i_253.jpg b/78430-h/images/i_253.jpg Binary files differnew file mode 100755 index 0000000..90b3ad2 --- /dev/null +++ b/78430-h/images/i_253.jpg diff --git a/78430-h/images/i_253a.jpg b/78430-h/images/i_253a.jpg Binary files differnew file mode 100755 index 0000000..2494496 --- /dev/null +++ b/78430-h/images/i_253a.jpg diff --git a/78430-h/images/i_253b.jpg b/78430-h/images/i_253b.jpg Binary files differnew file mode 100755 index 0000000..d33b90f --- /dev/null +++ b/78430-h/images/i_253b.jpg diff --git a/78430-h/images/i_254.jpg b/78430-h/images/i_254.jpg Binary files differnew file mode 100755 index 0000000..819135e --- /dev/null +++ b/78430-h/images/i_254.jpg diff --git a/78430-h/images/i_254a.jpg b/78430-h/images/i_254a.jpg Binary files differnew file mode 100755 index 0000000..c4001d4 --- /dev/null +++ b/78430-h/images/i_254a.jpg diff --git a/78430-h/images/i_255.jpg b/78430-h/images/i_255.jpg Binary files differnew file mode 100755 index 0000000..b031dba --- /dev/null +++ b/78430-h/images/i_255.jpg diff --git a/78430-h/images/i_256.jpg b/78430-h/images/i_256.jpg Binary files differnew file mode 100755 index 0000000..c7b6208 --- /dev/null +++ b/78430-h/images/i_256.jpg diff --git a/78430-h/images/i_256a.jpg b/78430-h/images/i_256a.jpg Binary files differnew file mode 100755 index 0000000..df0475a --- /dev/null +++ b/78430-h/images/i_256a.jpg diff --git a/78430-h/images/i_257.jpg b/78430-h/images/i_257.jpg Binary files differnew file mode 100755 index 0000000..6bb758b --- /dev/null +++ b/78430-h/images/i_257.jpg diff --git a/78430-h/images/i_257a.jpg b/78430-h/images/i_257a.jpg Binary files differnew file mode 100755 index 0000000..bb7c08e --- /dev/null +++ b/78430-h/images/i_257a.jpg diff --git a/78430-h/images/i_261.jpg b/78430-h/images/i_261.jpg Binary files differnew file mode 100755 index 0000000..552ed47 --- /dev/null +++ b/78430-h/images/i_261.jpg diff --git a/78430-h/images/i_263.jpg b/78430-h/images/i_263.jpg Binary files differnew file mode 100755 index 0000000..5931ec9 --- /dev/null +++ b/78430-h/images/i_263.jpg diff --git a/78430-h/images/i_265.jpg b/78430-h/images/i_265.jpg Binary files differnew file mode 100755 index 0000000..c9677c8 --- /dev/null +++ b/78430-h/images/i_265.jpg diff --git a/78430-h/images/i_266.jpg b/78430-h/images/i_266.jpg Binary files differnew file mode 100755 index 0000000..04aa13d --- /dev/null +++ b/78430-h/images/i_266.jpg diff --git a/78430-h/images/i_266a.jpg b/78430-h/images/i_266a.jpg Binary files differnew file mode 100755 index 0000000..daa94bc --- /dev/null +++ b/78430-h/images/i_266a.jpg diff --git a/78430-h/images/i_267.jpg b/78430-h/images/i_267.jpg Binary files differnew file mode 100755 index 0000000..426f9b2 --- /dev/null +++ b/78430-h/images/i_267.jpg diff --git a/78430-h/images/i_268.jpg b/78430-h/images/i_268.jpg Binary files differnew file mode 100755 index 0000000..18c0805 --- /dev/null +++ b/78430-h/images/i_268.jpg diff --git a/78430-h/images/i_268a.jpg b/78430-h/images/i_268a.jpg Binary files differnew file mode 100755 index 0000000..af5cf27 --- /dev/null +++ b/78430-h/images/i_268a.jpg diff --git a/78430-h/images/i_269.jpg b/78430-h/images/i_269.jpg Binary files differnew file mode 100755 index 0000000..c60ff22 --- /dev/null +++ b/78430-h/images/i_269.jpg diff --git a/78430-h/images/i_271.jpg b/78430-h/images/i_271.jpg Binary files differnew file mode 100755 index 0000000..a235dab --- /dev/null +++ b/78430-h/images/i_271.jpg diff --git a/78430-h/images/i_271a.jpg b/78430-h/images/i_271a.jpg Binary files differnew file mode 100755 index 0000000..dcbc8d4 --- /dev/null +++ b/78430-h/images/i_271a.jpg diff --git a/78430-h/images/i_271b.jpg b/78430-h/images/i_271b.jpg Binary files differnew file mode 100755 index 0000000..0a764a5 --- /dev/null +++ b/78430-h/images/i_271b.jpg diff --git a/78430-h/images/i_272.jpg b/78430-h/images/i_272.jpg Binary files differnew file mode 100755 index 0000000..0122b22 --- /dev/null +++ b/78430-h/images/i_272.jpg diff --git a/78430-h/images/i_272a.jpg b/78430-h/images/i_272a.jpg Binary files differnew file mode 100755 index 0000000..2ef7397 --- /dev/null +++ b/78430-h/images/i_272a.jpg diff --git a/78430-h/images/i_272b.jpg b/78430-h/images/i_272b.jpg Binary files differnew file mode 100755 index 0000000..d29d159 --- /dev/null +++ b/78430-h/images/i_272b.jpg diff --git a/78430-h/images/i_273.jpg b/78430-h/images/i_273.jpg Binary files differnew file mode 100755 index 0000000..5d2a8b9 --- /dev/null +++ b/78430-h/images/i_273.jpg diff --git a/78430-h/images/i_273a.jpg b/78430-h/images/i_273a.jpg Binary files differnew file mode 100755 index 0000000..190c380 --- /dev/null +++ b/78430-h/images/i_273a.jpg diff --git a/78430-h/images/i_273b.jpg b/78430-h/images/i_273b.jpg Binary files differnew file mode 100755 index 0000000..242eba3 --- /dev/null +++ b/78430-h/images/i_273b.jpg diff --git a/78430-h/images/i_274.jpg b/78430-h/images/i_274.jpg Binary files differnew file mode 100755 index 0000000..9853f0b --- /dev/null +++ b/78430-h/images/i_274.jpg diff --git a/78430-h/images/i_274a.jpg b/78430-h/images/i_274a.jpg Binary files differnew file mode 100755 index 0000000..df14f36 --- /dev/null +++ b/78430-h/images/i_274a.jpg diff --git a/78430-h/images/i_276.jpg b/78430-h/images/i_276.jpg Binary files differnew file mode 100755 index 0000000..4288afa --- /dev/null +++ b/78430-h/images/i_276.jpg diff --git a/78430-h/images/i_277.jpg b/78430-h/images/i_277.jpg Binary files differnew file mode 100755 index 0000000..480b5ef --- /dev/null +++ b/78430-h/images/i_277.jpg diff --git a/78430-h/images/i_278.jpg b/78430-h/images/i_278.jpg Binary files differnew file mode 100755 index 0000000..9b1fc42 --- /dev/null +++ b/78430-h/images/i_278.jpg diff --git a/78430-h/images/i_278a.jpg b/78430-h/images/i_278a.jpg Binary files differnew file mode 100755 index 0000000..48d1a1a --- /dev/null +++ b/78430-h/images/i_278a.jpg diff --git a/78430-h/images/i_282.jpg b/78430-h/images/i_282.jpg Binary files differnew file mode 100755 index 0000000..49c5c08 --- /dev/null +++ b/78430-h/images/i_282.jpg diff --git a/78430-h/images/i_284.jpg b/78430-h/images/i_284.jpg Binary files differnew file mode 100755 index 0000000..c52f644 --- /dev/null +++ b/78430-h/images/i_284.jpg diff --git a/78430-h/images/i_285.jpg b/78430-h/images/i_285.jpg Binary files differnew file mode 100755 index 0000000..3c781ec --- /dev/null +++ b/78430-h/images/i_285.jpg diff --git a/78430-h/images/i_285a.jpg b/78430-h/images/i_285a.jpg Binary files differnew file mode 100755 index 0000000..e54d856 --- /dev/null +++ b/78430-h/images/i_285a.jpg diff --git a/78430-h/images/i_286.jpg b/78430-h/images/i_286.jpg Binary files differnew file mode 100755 index 0000000..9c48d08 --- /dev/null +++ b/78430-h/images/i_286.jpg diff --git a/78430-h/images/i_288.jpg b/78430-h/images/i_288.jpg Binary files differnew file mode 100755 index 0000000..1e548a4 --- /dev/null +++ b/78430-h/images/i_288.jpg diff --git a/78430-h/images/i_289.jpg b/78430-h/images/i_289.jpg Binary files differnew file mode 100755 index 0000000..5077944 --- /dev/null +++ b/78430-h/images/i_289.jpg diff --git a/78430-h/images/i_290.jpg b/78430-h/images/i_290.jpg Binary files differnew file mode 100755 index 0000000..309bb73 --- /dev/null +++ b/78430-h/images/i_290.jpg diff --git a/78430-h/images/i_290a.jpg b/78430-h/images/i_290a.jpg Binary files differnew file mode 100755 index 0000000..c96640f --- /dev/null +++ b/78430-h/images/i_290a.jpg diff --git a/78430-h/images/i_291.jpg b/78430-h/images/i_291.jpg Binary files differnew file mode 100755 index 0000000..e74b73e --- /dev/null +++ b/78430-h/images/i_291.jpg diff --git a/78430-h/images/i_292.jpg b/78430-h/images/i_292.jpg Binary files differnew file mode 100755 index 0000000..6c73f21 --- /dev/null +++ b/78430-h/images/i_292.jpg diff --git a/78430-h/images/i_294.jpg b/78430-h/images/i_294.jpg Binary files differnew file mode 100755 index 0000000..759d4f2 --- /dev/null +++ b/78430-h/images/i_294.jpg diff --git a/78430-h/images/i_295.jpg b/78430-h/images/i_295.jpg Binary files differnew file mode 100755 index 0000000..0fee534 --- /dev/null +++ b/78430-h/images/i_295.jpg diff --git a/78430-h/images/i_298.jpg b/78430-h/images/i_298.jpg Binary files differnew file mode 100755 index 0000000..1105238 --- /dev/null +++ b/78430-h/images/i_298.jpg diff --git a/78430-h/images/i_300.jpg b/78430-h/images/i_300.jpg Binary files differnew file mode 100755 index 0000000..95ffc58 --- /dev/null +++ b/78430-h/images/i_300.jpg diff --git a/78430-h/images/i_300a.jpg b/78430-h/images/i_300a.jpg Binary files differnew file mode 100755 index 0000000..66ca99f --- /dev/null +++ b/78430-h/images/i_300a.jpg diff --git a/78430-h/images/i_303.jpg b/78430-h/images/i_303.jpg Binary files differnew file mode 100755 index 0000000..11ab9f4 --- /dev/null +++ b/78430-h/images/i_303.jpg diff --git a/78430-h/images/i_307.jpg b/78430-h/images/i_307.jpg Binary files differnew file mode 100755 index 0000000..288694d --- /dev/null +++ b/78430-h/images/i_307.jpg diff --git a/78430-h/images/i_307a.jpg b/78430-h/images/i_307a.jpg Binary files differnew file mode 100755 index 0000000..802cf26 --- /dev/null +++ b/78430-h/images/i_307a.jpg diff --git a/78430-h/images/i_308.jpg b/78430-h/images/i_308.jpg Binary files differnew file mode 100755 index 0000000..a80ab88 --- /dev/null +++ b/78430-h/images/i_308.jpg diff --git a/78430-h/images/i_308a.jpg b/78430-h/images/i_308a.jpg Binary files differnew file mode 100755 index 0000000..1814e48 --- /dev/null +++ b/78430-h/images/i_308a.jpg diff --git a/78430-h/images/i_310.jpg b/78430-h/images/i_310.jpg Binary files differnew file mode 100755 index 0000000..8b47271 --- /dev/null +++ b/78430-h/images/i_310.jpg diff --git a/78430-h/images/i_312.jpg b/78430-h/images/i_312.jpg Binary files differnew file mode 100755 index 0000000..813d5ba --- /dev/null +++ b/78430-h/images/i_312.jpg diff --git a/78430-h/images/i_313.jpg b/78430-h/images/i_313.jpg Binary files differnew file mode 100755 index 0000000..d51b6cc --- /dev/null +++ b/78430-h/images/i_313.jpg diff --git a/78430-h/images/i_314.jpg b/78430-h/images/i_314.jpg Binary files differnew file mode 100755 index 0000000..904ef60 --- /dev/null +++ b/78430-h/images/i_314.jpg diff --git a/78430-h/images/i_315.jpg b/78430-h/images/i_315.jpg Binary files differnew file mode 100755 index 0000000..feb6040 --- /dev/null +++ b/78430-h/images/i_315.jpg diff --git a/78430-h/images/i_318.jpg b/78430-h/images/i_318.jpg Binary files differnew file mode 100755 index 0000000..a7a4978 --- /dev/null +++ b/78430-h/images/i_318.jpg diff --git a/78430-h/images/i_319.jpg b/78430-h/images/i_319.jpg Binary files differnew file mode 100755 index 0000000..37b40ec --- /dev/null +++ b/78430-h/images/i_319.jpg diff --git a/78430-h/images/i_321.jpg b/78430-h/images/i_321.jpg Binary files differnew file mode 100755 index 0000000..caa2b7d --- /dev/null +++ b/78430-h/images/i_321.jpg diff --git a/78430-h/images/i_325.jpg b/78430-h/images/i_325.jpg Binary files differnew file mode 100755 index 0000000..ebf5c51 --- /dev/null +++ b/78430-h/images/i_325.jpg diff --git a/78430-h/images/i_327.jpg b/78430-h/images/i_327.jpg Binary files differnew file mode 100755 index 0000000..72e3a56 --- /dev/null +++ b/78430-h/images/i_327.jpg diff --git a/78430-h/images/i_328.jpg b/78430-h/images/i_328.jpg Binary files differnew file mode 100755 index 0000000..851898c --- /dev/null +++ b/78430-h/images/i_328.jpg diff --git a/78430-h/images/i_328a.jpg b/78430-h/images/i_328a.jpg Binary files differnew file mode 100755 index 0000000..30a7602 --- /dev/null +++ b/78430-h/images/i_328a.jpg diff --git a/78430-h/images/i_329.jpg b/78430-h/images/i_329.jpg Binary files differnew file mode 100755 index 0000000..a1ab666 --- /dev/null +++ b/78430-h/images/i_329.jpg diff --git a/78430-h/images/i_330.jpg b/78430-h/images/i_330.jpg Binary files differnew file mode 100755 index 0000000..accfca1 --- /dev/null +++ b/78430-h/images/i_330.jpg diff --git a/78430-h/images/i_331.jpg b/78430-h/images/i_331.jpg Binary files differnew file mode 100755 index 0000000..b9efd81 --- /dev/null +++ b/78430-h/images/i_331.jpg diff --git a/78430-h/images/i_334.jpg b/78430-h/images/i_334.jpg Binary files differnew file mode 100755 index 0000000..8f9c87b --- /dev/null +++ b/78430-h/images/i_334.jpg diff --git a/78430-h/images/i_334a.jpg b/78430-h/images/i_334a.jpg Binary files differnew file mode 100755 index 0000000..07af197 --- /dev/null +++ b/78430-h/images/i_334a.jpg diff --git a/78430-h/images/i_335.jpg b/78430-h/images/i_335.jpg Binary files differnew file mode 100755 index 0000000..d12c838 --- /dev/null +++ b/78430-h/images/i_335.jpg diff --git a/78430-h/images/i_335a.jpg b/78430-h/images/i_335a.jpg Binary files differnew file mode 100755 index 0000000..78e1af6 --- /dev/null +++ b/78430-h/images/i_335a.jpg diff --git a/78430-h/images/i_336.jpg b/78430-h/images/i_336.jpg Binary files differnew file mode 100755 index 0000000..3764c3f --- /dev/null +++ b/78430-h/images/i_336.jpg diff --git a/78430-h/images/i_336a.jpg b/78430-h/images/i_336a.jpg Binary files differnew file mode 100755 index 0000000..fd9df63 --- /dev/null +++ b/78430-h/images/i_336a.jpg diff --git a/78430-h/images/i_337.jpg b/78430-h/images/i_337.jpg Binary files differnew file mode 100755 index 0000000..72d4314 --- /dev/null +++ b/78430-h/images/i_337.jpg diff --git a/78430-h/images/i_337a.jpg b/78430-h/images/i_337a.jpg Binary files differnew file mode 100755 index 0000000..ae014b4 --- /dev/null +++ b/78430-h/images/i_337a.jpg diff --git a/78430-h/images/i_338.jpg b/78430-h/images/i_338.jpg Binary files differnew file mode 100755 index 0000000..0a08800 --- /dev/null +++ b/78430-h/images/i_338.jpg diff --git a/78430-h/images/i_339.jpg b/78430-h/images/i_339.jpg Binary files differnew file mode 100755 index 0000000..9fc137f --- /dev/null +++ b/78430-h/images/i_339.jpg diff --git a/78430-h/images/i_340.jpg b/78430-h/images/i_340.jpg Binary files differnew file mode 100755 index 0000000..a7ebfc5 --- /dev/null +++ b/78430-h/images/i_340.jpg diff --git a/78430-h/images/i_341.jpg b/78430-h/images/i_341.jpg Binary files differnew file mode 100755 index 0000000..5ff6278 --- /dev/null +++ b/78430-h/images/i_341.jpg diff --git a/78430-h/images/i_342.jpg b/78430-h/images/i_342.jpg Binary files differnew file mode 100755 index 0000000..1421d89 --- /dev/null +++ b/78430-h/images/i_342.jpg diff --git a/78430-h/images/i_343.jpg b/78430-h/images/i_343.jpg Binary files differnew file mode 100755 index 0000000..3420526 --- /dev/null +++ b/78430-h/images/i_343.jpg diff --git a/78430-h/images/i_345.jpg b/78430-h/images/i_345.jpg Binary files differnew file mode 100755 index 0000000..d117ebb --- /dev/null +++ b/78430-h/images/i_345.jpg diff --git a/78430-h/images/i_346.jpg b/78430-h/images/i_346.jpg Binary files differnew file mode 100755 index 0000000..c81e155 --- /dev/null +++ b/78430-h/images/i_346.jpg diff --git a/78430-h/images/i_347.jpg b/78430-h/images/i_347.jpg Binary files differnew file mode 100755 index 0000000..1a8da6b --- /dev/null +++ b/78430-h/images/i_347.jpg diff --git a/78430-h/images/i_347a.jpg b/78430-h/images/i_347a.jpg Binary files differnew file mode 100755 index 0000000..3a7f698 --- /dev/null +++ b/78430-h/images/i_347a.jpg diff --git a/78430-h/images/i_348.jpg b/78430-h/images/i_348.jpg Binary files differnew file mode 100755 index 0000000..477cf80 --- /dev/null +++ b/78430-h/images/i_348.jpg diff --git a/78430-h/images/i_351.jpg b/78430-h/images/i_351.jpg Binary files differnew file mode 100755 index 0000000..b1a38d1 --- /dev/null +++ b/78430-h/images/i_351.jpg diff --git a/78430-h/images/i_352.jpg b/78430-h/images/i_352.jpg Binary files differnew file mode 100755 index 0000000..430b242 --- /dev/null +++ b/78430-h/images/i_352.jpg diff --git a/78430-h/images/i_353.jpg b/78430-h/images/i_353.jpg Binary files differnew file mode 100755 index 0000000..d5043f0 --- /dev/null +++ b/78430-h/images/i_353.jpg diff --git a/78430-h/images/i_353a.jpg b/78430-h/images/i_353a.jpg Binary files differnew file mode 100755 index 0000000..f552c1b --- /dev/null +++ b/78430-h/images/i_353a.jpg diff --git a/78430-h/images/i_355.jpg b/78430-h/images/i_355.jpg Binary files differnew file mode 100755 index 0000000..43f0b28 --- /dev/null +++ b/78430-h/images/i_355.jpg diff --git a/78430-h/images/i_357.jpg b/78430-h/images/i_357.jpg Binary files differnew file mode 100755 index 0000000..c516f3f --- /dev/null +++ b/78430-h/images/i_357.jpg diff --git a/78430-h/images/i_357a.jpg b/78430-h/images/i_357a.jpg Binary files differnew file mode 100755 index 0000000..0377e21 --- /dev/null +++ b/78430-h/images/i_357a.jpg diff --git a/78430-h/images/i_358.jpg b/78430-h/images/i_358.jpg Binary files differnew file mode 100755 index 0000000..044e86f --- /dev/null +++ b/78430-h/images/i_358.jpg diff --git a/78430-h/images/i_358a.jpg b/78430-h/images/i_358a.jpg Binary files differnew file mode 100755 index 0000000..21b5ae4 --- /dev/null +++ b/78430-h/images/i_358a.jpg diff --git a/78430-h/images/i_359.jpg b/78430-h/images/i_359.jpg Binary files differnew file mode 100755 index 0000000..b688803 --- /dev/null +++ b/78430-h/images/i_359.jpg diff --git a/78430-h/images/i_360.jpg b/78430-h/images/i_360.jpg Binary files differnew file mode 100755 index 0000000..5dd4f3e --- /dev/null +++ b/78430-h/images/i_360.jpg diff --git a/78430-h/images/i_361.jpg b/78430-h/images/i_361.jpg Binary files differnew file mode 100755 index 0000000..3b11813 --- /dev/null +++ b/78430-h/images/i_361.jpg diff --git a/78430-h/images/i_363.jpg b/78430-h/images/i_363.jpg Binary files differnew file mode 100755 index 0000000..fc9f14c --- /dev/null +++ b/78430-h/images/i_363.jpg diff --git a/78430-h/images/i_366.jpg b/78430-h/images/i_366.jpg Binary files differnew file mode 100755 index 0000000..c5abfe1 --- /dev/null +++ b/78430-h/images/i_366.jpg diff --git a/78430-h/images/i_371.jpg b/78430-h/images/i_371.jpg Binary files differnew file mode 100755 index 0000000..50e9d8a --- /dev/null +++ b/78430-h/images/i_371.jpg diff --git a/78430-h/images/i_378.jpg b/78430-h/images/i_378.jpg Binary files differnew file mode 100644 index 0000000..a7d0c53 --- /dev/null +++ b/78430-h/images/i_378.jpg diff --git a/LICENSE.txt b/LICENSE.txt new file mode 100644 index 0000000..6c72794 --- /dev/null +++ b/LICENSE.txt @@ -0,0 +1,11 @@ +This book, including all associated images, markup, improvements, +metadata, and any other content or labor, has been confirmed to be +in the PUBLIC DOMAIN IN THE UNITED STATES. + +Procedures for determining public domain status are described in +the "Copyright How-To" at https://www.gutenberg.org. + +No investigation has been made concerning possible copyrights in +jurisdictions other than the United States. Anyone seeking to utilize +this eBook outside of the United States should confirm copyright +status under the laws that apply to them. diff --git a/README.md b/README.md new file mode 100644 index 0000000..5b3425a --- /dev/null +++ b/README.md @@ -0,0 +1,2 @@ +Project Gutenberg (https://www.gutenberg.org) public repository for eBook #78430 +(https://www.gutenberg.org/ebooks/78430) |
