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| author | nfenwick <nfenwick@pglaf.org> | 2025-02-07 14:07:46 -0800 |
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| committer | nfenwick <nfenwick@pglaf.org> | 2025-02-07 14:07:46 -0800 |
| commit | 80f40157a83de600ef48fba676419325fbad1bdd (patch) | |
| tree | 38e4559080ce414b6593c7c6a95cc18ccc08daf1 | |
| parent | cc432c9173a868398aa941cd4fbbbe90ce753f10 (diff) | |
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diff --git a/.gitattributes b/.gitattributes new file mode 100644 index 0000000..d7b82bc --- /dev/null +++ b/.gitattributes @@ -0,0 +1,4 @@ +*.txt text eol=lf +*.htm text eol=lf +*.html text eol=lf +*.md text eol=lf diff --git a/LICENSE.txt b/LICENSE.txt new file mode 100644 index 0000000..6312041 --- /dev/null +++ b/LICENSE.txt @@ -0,0 +1,11 @@ +This eBook, 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..7006729 --- /dev/null +++ b/README.md @@ -0,0 +1,2 @@ +Project Gutenberg (https://www.gutenberg.org) public repository for +eBook #55382 (https://www.gutenberg.org/ebooks/55382) diff --git a/old/55382-0.txt b/old/55382-0.txt deleted file mode 100644 index 10da295..0000000 --- a/old/55382-0.txt +++ /dev/null @@ -1,10133 +0,0 @@ -The Project Gutenberg EBook of Field Book of Common Rocks and Minerals, by -Frederic Brewster Loomis and Walter Everett Corbin - -This eBook is for the use of anyone anywhere in the United States and most -other parts of the world at no cost and with almost no restrictions -whatsoever. You may copy it, give it away or re-use it under the terms of -the Project Gutenberg License included with this eBook or online at -www.gutenberg.org. If you are not located in the United States, you'll have -to check the laws of the country where you are located before using this ebook. - -Title: Field Book of Common Rocks and Minerals - For identifying the Rocks and Minerals of the United States - and interpreting their Origins and Meanings - -Author: Frederic Brewster Loomis - Walter Everett Corbin - -Release Date: August 18, 2017 [EBook #55382] - -Language: English - -Character set encoding: UTF-8 - -*** START OF THIS PROJECT GUTENBERG EBOOK FIELD BOOK OF COMMON ROCKS *** - - - - -Produced by Stephen Hutcheson, Dave Morgan and the Online -Distributed Proofreading Team at http://www.pgdp.net - - - - - - - - - - Field Book _of_ - Common Rocks - _and_ Minerals - - - For identifying the Rocks and Minerals of the United States and - interpreting their Origins and Meanings - - - By - Frederic Brewster Loomis - Late Professor of Mineralogy and Geology - in Amherst College - - - With 47 Colored Specimens and over 100 other Illustrations from - Photographs by W. E. Corbin and drawings by the Author - - - G. P. Putnam’s Sons - New York and London - - FIELD BOOK - OF - COMMON ROCKS AND MINERALS - - Copyright, 1923, 1948 - by - Frederick Brewster Loomis - - Twenty-sixth Impression - Revised 1948 - - All rights reserved. This book, or parts thereof, must not be - reproduced in any form without permission. - - Made in the United States of America - - - Dedicated - TO - MY MOTHER - WHO ENCOURAGED ME WHILE A BOY TO GATHER MINERALS, ROCKS AND FOSSILS. - - - - - PREFACE - - -Everyone, who is alert as he wanders about this world, wants to know -what he is seeing and what it is all about. Here and there with the aid -of capable guides a few have been introduced into the sphere of that -wide and fascinating knowledge of Nature which has been so rapidly -accumulated during this and the latter part of the last century. It is a -full treasure house constantly being enriched, but unfortunately the few -who have been initiated have soon acquired a technical language and -habit, so that their knowledge and new acquisitions are communicated to -but few. The public at large, not having the language nor an interpreter -at hand, has come almost at once to a barrier which few have the time or -patience to surmount. - -Latterly it has become clear that the largest progress cannot be made if -the knowledge of any branch of Science is confined to a few only. The -most rapid advances have been made where many men are interested and -enthusiastic. In no science should there be a difficult barrier between -the amateur and the professional student. All Nature is equally open for -everyone to study, and there should never be created obstacles as by the -use of terminology not easily acquired by anyone. Of late these barriers -have been in part broken down and competent students have written guides -which anyone can follow, and soon begin to know the plants, trees, -birds, insects, etc. So far no one has attempted to make the study of -minerals and rocks so direct and simple that everyone can get a start. -Most books on minerals, and practically all those on rocks are written -for school courses, and to say the least chill any enthusiasm which is -naturally aroused by the finding of interesting looking rocks or -minerals. - -The purpose of this book is first of all to provide a means of -identifying minerals and rocks by such methods as are practical without -elaborate equipment or previous training: and second to suggest the -conditions under which the various minerals and rocks were formed, so -that, at the first contact, one may get a conception of the events which -have anteceded the mineral or rock which has been found. For this -purpose keys have been worked out for determining the rocks and minerals -by such obvious features as color, hardness, etc. Each mineral or rock -is introduced by a summary of its characters, then the features by which -it may be distinguished from any other similar mineral are given, after -which its mode of origin and its meanings are considered. For those -interested in the composition of the minerals, it is given in chemical -symbols with each mineral. Most classifications of minerals are based on -the composition, all the sulphides, carbonates, etc., being grouped -together, but in this book, because the popular interest and commercial -uses are primarily in the metal present, the minerals are grouped in -each case about the chief metal, all the minerals of iron being grouped -together, for instance. - -A few minerals and rocks which are not strictly common have been -included such as gems and meteorites; the gems because they are of -intense interest to their owners and are often simply perfect examples -of a fairly common mineral; and such forms as meteorites because it is -important that, if one should run across one, it should be recognized, -and so not lost to the world. - -The book is freely illustrated, those minerals in which color is -important for identification being illustrated in colors, and those -which are black, or in which the color is not a determining factor, are -shown in either photographic or outline figures. - -In the introductory chapter there are explanations of the terms used in -describing minerals, and of the systems in which they are grouped. A -knowledge of the systems may not be a necessity, but it is a great help -in determining minerals, and is very important in understanding why the -individual minerals take the varied forms which are characteristic of -them. These systems will be better understood after a few minerals have -been gathered and examined. - -It is hoped the book will help those who have already some knowledge of -rocks and minerals, and especially that it will tempt many to begin an -acquaintance with the rocks and minerals which are all about them, and -are the foundation on which our material progress is built. Rocks and -minerals have some advantages over most objects which are collected in -that they neither require special preparation before they can be kept, -nor do they deteriorate with time. - -The author will appreciate corrections or suggestions as to better -presentation of the material in this book. - - F. B. L. - -Amherst, Mass. - - - - - CONTENTS - - - PAGE - Preface vii - CHAPTER - I.—An Introduction 3 - II.—On the Forms and Properties of Minerals 10 - III.—The Minerals 25 - IV.—The Rocks 170 - V.—Miscellaneous Rocks 248 - Bibliography 270 - Index 273 - - - - - LIST OF PLATES - (AT END OF BOOK) - - - PAGE - Tourmaline crystals, growing amid feldspar crystals in a cavity in - granite, from Paris, Me. 279 - Plate 1.—Basal forms of the isometric system 311 - Plate 2.—Basal forms of the tetragonal system. Basal forms of the - orthorhombic system 312 - Plate 3.—Basal forms of the monoclinic system. A cross section of - the prism with its edges beveled so that a six-sided prism - is formed (pseudo-hexagonal). Basal form of the triclinic - system. 313 - Plate 4.—Basal forms of the hexagonal system 314 - Plate 5.—Gold in quartz from California (_in color_) 280 - Plate 6.—Native silver in calcite. Argentite, the black masses - throughout the white quartz (_in color_) 281 - Plate 7.—Pyrargyrite as it appears after moderate exposure to the - light; streak at left. Crystal form of pyrargyrite. - Prousite as it appears after moderate exposure to the - light; streak at left (_in color_) 282 - Plate 8.—Native copper from Michigan. Chalcopyrite in tetrahedrons - and an occasional octahedron; streak to the left (_in - color_) 283 - Plate 9.—Chalcocite crystals with the bluish tarnish. Tetrahedrite - crystals; streak to left (_in color_) 284 - Plate 10.—Tetrahedrons showing characteristic manner in which - tetrahedrite occurs. A cube with the edges beveled and the - corners cut in a form characteristic of cuprite 315 - Plate 11.—Cuprite, the red crystals showing characteristic color, - others showing the green tarnish of malachite. Malachite - (green) and azurite (blue), the two minerals shown - together as they very commonly occur (_in color_) 285 - Plate 12.—Limonite. The crystal form in which goethite is found - (_in color_) 286 - Plate 13.—Hematite. Clinton iron ore, oolitic. Siderite crystals - (_in color_) 287 - Plate 14.—Crystal forms of hematite. A typical crystal of - magnetite. The rhombohedron typical of siderite 317 - Plate 15.—Pyrite crystals. Marcasite in concretionary form with - radiate structure (_in color_) 288 - Plate 16.—The pyritohedron. The pyritohedron with certain of its - edges beveled by the cube faces, to show the relationship - of these two forms 318 - Plate 17.—Galena in crystals. Pyromorphite crystals (Green) (_in - color_) 289 - Plate 18.—Typical forms for cerrusite. Forms in which anglesite - occurs 319 - Plate 19.—Sphalerite, some the normal yellow and some crystals - with the reddish tinge. (White is dolomite.) Zincite, - streak to the left (_in color_) 290 - Plate 20.—A characteristic form in which sphalerite may occur. - Characteristic form for zincite crystals. Typical form of - crystal of willemite 320 - Plate 21.—Smithsonite in yellow crystals. Franklinite in - octahedral crystals, streak to left (_in color_) 291 - Plate 22.—Moss agates, showing the dendritic growth of manganitic - minerals, like manganite or pyrolusite. Crystal form of - manganite 321 - Plate 23.—Crystals of green corundum in syenite, from Montana. - Typical crystal forms of corundum 322 - Plate 24.—Arsenopyrite, showing crystals massed so as to be - incompletely developed. Realgar as it usually occurs in - powdery incrustations (_in color_) 292 - Plate 25.—Large crystals of stibnite; the light colored face is - the one parallel to which cleavage occurs. Niccolite is a - vein in slate (_in color_) 293 - Plate 26.—Cobaltite, silver color, with pink tinge. Smaltite, pink - is cobalt bloom (_in color_) 294 - Plate 27.—Carnotite from Southwest Colorado. Cinnabar (_in color_) 295 - Plate 28.—Cassiterite, twinned crystals. The crystal form in which - both cassiterite and rutile occur when in simple crystals. - Multiple twinning characteristic of rutile 323 - Plate 29.—Crystal of spinel. Crystal forms in which dolomite - occurs 324 - Plate 30.—Two intergrowing or twinned quartz crystals. Diagram of - the typical quartz crystal. A quartz crystal on which the - left hand rhombohedron is represented by small faces, - while the right hand rhombohedron has large faces 316 - Plate 31.—Amethyst, not however deep enough colored for gems. - Jasper, with botryoidal surface (_in color_) 296 - Plate 32.—Banded agate from Brazil (_in color_) 297 - Plate 33.—Common opal from Arizona. Siliceous sinter or geyserite - from Yellowstone Park (_in color_) 298 - Plate 34.—Orthoclase, a cleavage piece. Crystal forms of - orthoclase. Diagram of a multiple twin of a plagioclase - feldspar 325 - Plate 35.—A group of microcline crystals from Pike’s Peak, Colo. - Labradorite, showing multiple twinning (the striation) and - the iridescent play of colors (_in color_) 299 - Plate 36.—Crystal form of a pyroxene. Cross sections of a pyroxene - crystal showing the lines of intersection of two cleavage - planes. Cross sections of pyroxenes, showing typical forms - taken by crystals. Augite crystals, in crystalline - limestone (_in color_) 300 - Plate 37.—Diagrams of amphibole crystals. Tremolite in silky - fibrous crystals, asbestos. Hornblende crystals in - quartzite 326 - Plate 38.—The dodecahedron and the 24-sided figure characteristic - of garnets. The garnet, grossularite. The garnet, - alamandite (_in color_) 301 - Plate 39.—Beryl of gem quality. Zircon in syenite (_in color_) 302 - Plate 40.—Cyanite crystals in schist. A crystal of mica, showing - basal cleavage (_in color_) 303 - Plate 41.—Crystal form typical of topaz. A topaz crystal from - Brazil. Crystal form typical of staurolite when simple. A - typical twin of staurolite (_in color_) 304 - Plate 42.—Epidote crystals. Typical forms of epidote crystals. - Typical forms of tourmaline 327 - Plate 43.—Serpentine. Chlorite (_in color_) 305 - Plate 44.—The typical form of analcite. A typical natrolite - crystal. The typical crystal form of stilbite. A - sheaf-like bundle of fibrous crystals, typical of stilbite 329 - Plate 45.—A group of calcite crystals. Typical forms of calcite 330 - Plate 46.—Typical forms of aragonite. Typical form of the - anhydrite crystal 331 - Plate 47.—A piece of gypsum looking on the surface of the perfect - cleavage, and showing the two other cleavages as lines, - intersecting at 66°. Twinning is also shown. A simple - crystal of gypsum. Twin crystals of gypsum. 332 - Plate 48.—A group of barite crystals. Outline of the typical - tabular barite crystal. The six-sided double pyramid, - composed of three interpenetrating crystals, typical of - witherite and strontianite 328 - Plate 49.—Apatite crystals in crystalline calcite. The ends of - apatite crystals showing common modes of termination (_in - color_) 306 - Plate 50.—A group of fluorite crystals. A group of halite crystals - (_in color_) 307 - Plate 51.—Sulphur crystals. Ice crystals, the top one, the end of - a hexagonal prism; the two lower figures multiple twins as - in snow flakes 333 - Plate 52.—The Devil’s Tower, Wyoming, an example of igneous rock - with columnar structure, and resting on sedimentary rocks 334 - Courtesy of the U. S. Geological Survey - Plate 53.—A coarse granite. Graphic granite 335 - Plate 54.—Syenite. Gabbro 336 - Plate 55.—Basalt-porphyry. The large white crystals are - phenocrysts of plagioclase feldspar. Basalt-obsidian 337 - Plate 56.—Amgydoloid 338 - Plate 57.—The north face of Scott’s Bluff, Neb., showing - sedimentary sandstones above and clays below. The type of - erosion is characteristic of arid regions 339 - Courtesy of the U. S. Geological Survey - Plate 58.—Breccia. Conglomerate 340 - Plate 59.—Calcareous shale. Coquina 341 - Plate 60.—Foramenifera from chalk; enlarged about 25 diameters. - Encrinal limestone; fragments of the stems, arms and body - of crinoids 342 - Plate 61.—Amber. Two bottles of petroleum, the left hand one with - a paraffin base, the right hand one with an asphalt base - (_in color_) 308 - Plate 62.—Diatomaceous earth magnified 50 times. Two diatoms from - the above enlarged 250 times 343 - After Gravelle, by the courtesy of Natural History - Plate 63.—A metamorphic rock, showing the contortion of layers due - to expansion under heat 344 - Plate 64.—A conglomerate partly metamorphosed to a gneiss. A - typical gneiss 345 - Plate 65.—Mica schist, with garnets. Chlorite schist (_in color_) 309 - Plate 66.—Phyllite. A white marble, with black streaks due to - graphite 346 - Plate 67.—Serpentine composed of serpentite, hematite, and some - calcite (_in color_) 310 - Plate 68.—Claystones, simple and compound. A lime concretion, - which on splitting disclosed a fern leaf of the age of the - coal measures 347 - Plate 69.—A septeria from Seneca Lake, N. Y. Pisolite from Nevada 348 - Plate 70.—A geode filled with quartz crystals 349 - Plate 71.—A quartz pebble from the bed of a New England brook. A - pebble of schist and granite from the foot of Mt. Toby, - Mass. 350 - Plate 72.—An iron-nickel meteorite, of 23 lbs., which fell in - Claiborne Co., Tenn. An etched slice of an iron meteorite - which fell in Reed City, Osceola, Co., Mich. 351 - Plate 73.—A stone meteor, about natural size, which fell in 1875 - in Iowa Co., Iowa 352 - - - - - FIELD BOOK OF - COMMON ROCKS AND MINERALS - - - - - CHAPTER I - AN INTRODUCTION - - -Why - -Why should one be interested in rocks and minerals? Because the whole -world is made of rocks and minerals. They are the foundations on which -we build. From them we draw all our metals, and the extent to which we -utilize our minerals is a measure of the advance of our civilization. -Fragments of rock are the soil from which, by way of the plants, we draw -our food, and ultimately our life. The rocks make wild or gentle -scenery, one at least of the sources of pleasure. Knowledge of rocks and -minerals is then knowledge of fundamentals, of ultimate sources. Between -finding the raw materials and their present uses there are usually many -steps (so many that we forget that the beginning and end are united), as -for instance in your watch. It is made of gold, brass, steel, agate, -glass, and perhaps has luminous radium paint on the hands. It is a long -way from finding and mining gold, chalcopyrite, hematite, carnotite, -etc., through the raw materials, gold, copper, iron, etc., to the -finished watch, but the minerals are the foundations of the watch; and -it took centuries to find them and learn one by one how to use them, -from the gold 10,000 years ago down to the radium within the last fifty -years. Then too there is joy in going out into Nature’s wild and raw -places, joy in being on the foundations of the earth, joy in the -scenery, in the beauty of the minerals themselves. - -But why collect the rocks and minerals? First because this is the way to -know them. Both mineral and rocks require careful examination in order -to see all those fine points by which they are distinguished. It is -often necessary to compare one with another to get in mind the -differences of form, color, streak, though with increasing familiarity -these characteristics are recognized at first sight. It is the repeated -examination which makes a rock tell the story of the country from which -it came. Our first attempts to read the story give us only the most -general facts. Nature’s book, written in the rocks, has to be read -closely, often between the lines. Until we are used to the characters in -which the words are written, we read slowly. When they look at Nature’s -book, always open, most people do not read; for they do not know their -letters. Every mineral is a letter, every rock a word, and we learn to -read as we learn the minerals and rocks, and every time we go over them -we get more facts coming out. The place where a rock or mineral occurs -is of course the relation between them, and is involved in reading the -story. No one today is a perfect reader. We are all learning to see more -in the rocks day by day. So it is important to have the rocks and -minerals where they can be handled and repeatedly examined, where we can -turn to them in our leisure moments. Don’t stop when you have learned -the name of a mineral or rock. You need more. See what it means. -Secondly, minerals have beauties of form, color, and structure, and they -do not fade. They will be as perfect in ten years as when found. We are -all naturally crows, and love to gather the objects which interest us. -It is not a bad habit, and only needs directing. Cultivate it. Have a -hobby, and minerals and rocks are a good one; for they are like -treasures in Heaven which “neither moth nor rust doth corrupt.” Not only -will they give you pleasure, but they will be a constructive education, -training the eye to see, and the mind to think straight. No one ever -regretted the time and effort spent in collecting either minerals or -rocks. - - -Collecting - -In order to make a collection valuable two or three rules must be -observed. In the case of rocks, collect large enough samples so that -they will be characteristic, and clear in their make-up. The standard -size for rocks is 3 × 4 inches on top and one to two inches thick -according to the nature of the rock. Tiny fragments do not give the -character of the rock as well, and they are all the time getting into -confusion. Every specimen should be labeled, with at least its name and -the exact locality from which it came. Composition, structural features, -associations, and classification may be added, the more the better; for -each item adds to the information and interest of the specimen. One may -make his own labels or have printed blanks, and may put as much care and -art into the labels as desired, the more the better. One thing is very -important and that is to have a number on the label with a corresponding -one on the specimen, so that in case they should get separated, they may -be readily brought together, even by one who is not familiar with the -individual specimens. Lastly, give your collection as good a place as -possible, either in drawers, boxes or in a case. The specimens are worth -being kept in order and where they can be readily seen and compared. -Nature is systematic, and there is a reason for the order in which rocks -and minerals are taken up. It is desirable either that this order, or -some one of the orders of Nature appear in the collection. In this book -the metals are the basis of classification, all those minerals primarily -related to one of the metals being grouped together. - -In collecting minerals, the size of the specimens can not be so -regularly followed, but it should be followed when collecting -non-crystalline minerals, and when possible. Crystals however are chosen -from a variety of points of view, as perfection of form, color, examples -of cleavage, twinning, etc.; so that in many cases smaller or larger -examples must appear in the collection. It is always desirable that as -many variations of a rock or mineral as possible should appear in the -collection, and in many cases examples of the matrix from which the -crystals came. When crystals are tiny, it is well to place them in -vials, that they may not be lost. - - -Where - -Where shall we start in making a collection? Near home. Get the local -minerals and rocks first, and then range as widely as possible. The best -places are bare and exposed rocks, especially where fresh and -un-weathered surfaces are available. Quarries and where there has been -blasting along roads offer fine opportunities. Fissures and cavities in -the rocks are especially likely to have fine crystals, and in all -localities continued search will reveal a surprising number of different -minerals. The greatest variety occur in metamorphic rocks, or where -igneous rocks come in contact with other rocks, but even the sedimentary -rocks have a goodly range of minerals. All through the glaciated regions -of the northern United States lie scattered boulders brought from afar, -which will yield a surprising number of minerals and variety of rocks. - - -Equipment - -One may start with a very simple equipment, a geologist’s or stone -mason’s hammer which can be obtained at any hardware store, being -sufficient for field work. Rocks should be broken, so as to show fresh -surfaces and to get below the disintegrating effects of weathering. At -home one should have a streak plate (a piece of unglazed porcelain), a -set of hardness minerals (see page 20), and a small bottle each of -hydrochloric and nitric acid. A pocket lens is useful in order to see -more clearly the form of small minerals. These things can be purchased -of any Naturalist’s Supply Co., like Ward’s Natural Science -Establishment, P.O. 24, Beachwood Sta., Rochester, N. Y., or the -Kny-Scheerer Corp., 483 First Ave., New York City. Success depends upon -a quick eye, and persistent hunting. When traveling, opportunities are -offered at frequent intervals to see and get new specimens. - - -Study Your Collection - -Be sure and see the meaning in each rock and mineral. The history of the -country is revealed in its rocks and minerals. Note whether the rocks -are horizontal or folded, whether they change character from place to -place, or vertically. In going over a piece of country you may locate an -ancient mountain system now leveled, by noting a series of metamorphic -rocks, with a central core of granite, the roots of former mountains. -Don’t be afraid to draw conclusions from what you see. Later, when the -opportunity offers, look up the region in the geological folio, -bulletin, or map of that section, and check up your findings. These -geological folios and bulletins, of which there is one for nearly every -region, are a great help to collectors in suggesting where to look for -various rocks and minerals. Write to the Director of the U. S. -Geological Survey, Washington, D. C., for a catalogue of the -publications of the United States Survey, or find out from him what are -the maps or folios for the region in which you are interested. These U. -S. publications cost but little. When opportunity presents itself, visit -other collections. In them you will see some of the minerals or rocks -which have puzzled you, and there is nothing quite so satisfactory as -seeing the rocks or minerals themselves. No description can always be so -convincing. Then too you will get suggestions as to localities that you -can visit. - - -Literature - -As your collection grows, if you find you have special interest in one -or another branch of the field, you can get books giving more details in -that line; and at the back of this book will be found a list of such -books. - - - - - CHAPTER II - ON THE FORMS AND PROPERTIES OF MINERALS - - -Rocks - -All we know of the earth by direct observation is confined to less than -four miles depth; though by projecting downward the layers of rock that -come to the surface, we may fairly assume a knowledge of the structure -down to six or eight miles depth. This outer portion is often referred -to as the “crust of the earth,” but the idea that the deeper portions -are molten is no longer held. This outer portion is made of rocks, and a -rock may be defined as, _a mass of material, loose or solid, which makes -up an integral part of the earth_, as granite, limestone, or sand. The -rocks (except glassy igneous ones) are aggregates of one or more -minerals; either in their original form like the quartz, feldspar and -mica of granite, or in a secondary grouping, resulting from the units -having been dislodged from their primary position and regrouped a second -time, as in sandstone or clay. - - -Minerals - -Since the rocks are aggregates of minerals, it is best to take up the -minerals first. A mineral may be defined as _a natural inorganic -substance of definite chemical composition_. It is usually solid, -generally has crystalline structure, and may or may not be bounded by -crystal faces. _A crystal is a mineral, bounded by symmetrically grouped -faces, which have definite relationships to a set of imaginary lines -called axes._ There are between 1100 and 1200 minerals, of which 30 are -so frequently present, and so dominant in making up the rocks, that they -are termed _rock-forming minerals_. About 150 more occur frequently -enough so that they can be termed common minerals, and one may expect to -find a fairly large proportion of them. Some of these are abundant in -one part of the country and rare in others, but this book is written to -cover the United States, and so all those which have a fair abundance -are included, though some will only be found in the west and others -mostly in the east. Then there are some more minerals which are really -rare, but which are cherished because of their beauty of color, and are -used as gems. These are mentioned, and many of the gems are simply clear -and beautiful examples of minerals, which in dark or cloudy forms are -much more common. If one finds any of these rare minerals which are not -mentioned in this book, he must turn to one of the larger mineralogies -mentioned in the literature list to determine them. - - -Crystal Structure - -A crystal is a mass of molecules, all of the same composition. A -molecule in its turn is made up of atoms, and each atom is a unit mass -of an element. Thus the calcite molecule is made up of one unit or atom -of calcium, one of carbon, and three of oxygen (CaCO₃). These atoms are -held together by an attraction, and make a molecule, and for the study -of minerals the molecule is the unit. The mineral, calcite, is a mass of -molecules all like the one above, and each molecule so small as to be -invisible even with the aid of the most powerful microscope. When -calcite is in crystal form, the molecules, like ranks of soldiers, are -arranged each in its place, each at a definite distance from the other. -While each molecule may vibrate or wiggle within certain limits it does -not leave its place. (The comparison with soldiers is a good one for the -molecules of one layer, but it must be remembered that in a crystal -there are also like spacings and ranks up and down as well.) As long as -the molecules remain in fixed ranks, up and down, forward and back, and -sideways, the crystal is perfect. Calcite may be heated until it melts -and becomes liquid. Then the molecules leave their definite arrangement -and move about in all sorts of directions, like the soldiers after ranks -have broken. So long as the molecules are thus free to move about but -keep together, the substance is a liquid. There are cases when the -molecules in this disorder take fixed positions without falling into -ranks. Such minerals are non-crystalline and usually appear glassy. If -still greater heat is applied to the mineral in liquid form, a point is -reached (the vapor point), above which the molecules go flying away from -each (like soldiers in a panic), each seeking to get as far from the -other as possible, so only a container will prevent their dissipation. -When in this condition a mineral is gaseous. When cooled, the reverse -order obtains. The molecules of gas gather into a miscellaneous mob or -liquid: and if this is further cooled (but not too suddenly), they fall -into ranks and make a crystal. This may be illustrated with water. When -above 212° F. it is steam (molecules wildly dissipated); when between -212° and 32° it is water (molecules close to each other, but milling -like a herd of cattle); and when below 32° it is ice, the molecules -ranged in perfect order, rank on rank. - - -Crystal Systems - -With all the possible forms that crystals can and do take, there are six -systems of arrangement. First there is the case where ranks, files, and -vertical rows are all equal, and now to be scientific, instead of -talking about ranks, files, etc., we use the term axes to express these -ideas; the files or arrangements from front to back, being called the _a -axis_, the ranks, or side to side arrangement the _b axis_, and the -vertical arrangement the _c axis_. (See Plate 1.) These axes are -imaginary lines, but they represent real forces. - - -Isometric system - -When the axes are all equal and at right angles to each other, a crystal -is said to be in the isometric system. The cube is the basal form and -each side is known as a face. The ends of the axes come to the middle of -the cube faces. The essential feature of this system is that whatever -happens to one axis must happen to all, which is another way of saying -that all the axes are equal. If we think of the cube as having the -corners cut off, we would have a new face on each of the eight corners, -in addition to the six cube faces. Then if each of these new faces were -enlarged until they met and obliterated the cube faces, an eight-sided -figure, the octahedron, would result. In this the axes would ran to the -corners. Another modification of the cube would be to bevel each of its -twelve edges, making twelve new faces in addition to the six cube faces. -If we think of these new faces being developed until they meet and -obliterate the cube faces, there will result a twelve-sided figure, the -dodecahedron. And the 24 edges of the dodecahedron could be beveled to -make a 24-sided figure, and so on. Of course in Nature the corners are -not cut, nor the edges beveled, but as a result of the interaction of -the forces expressed by the axes and the distribution of the molecules, -the molecules arrange themselves in a cube, octahedron, dodecahedron or -combination of these basal forms. - - -Crystal formation - -Crystals are formed in liquids as they cool or evaporate and can no -longer hold the minerals in solution. Crystals start about a center or -nucleus, and molecule by molecule, the orderly arrangement is increased -and the crystal grows, there being no size which is characteristic. If -free in the liquid the crystal grows perfectly on all sides, but if -crystals are growing side by side, there comes a time when they -interfere with each other. Then the free faces continue to grow and the -orderly internal arrangement is maintained, though externally there is -interference. - - -Tetragonal system - -In the second or tetragonal system one axis (the c axis) is different -from the other two, but all three are still at right angles with each -other. This is saying scientifically that the lines of force are greater -or less in one direction than in the other two, but they act at right -angles to each other. The a and the b axes are equal and anything that -happens to one of these two must happen to the other, but need not -happen to the c axis. Thinking of the molecules that arrange themselves -under this system of forces, it is clear that the simplest form will be -a square prism, _i.e._, front to back, and from side to side the numbers -of molecules will be equal, but up and down there will be a greater or -lesser number. If the eight corners of this prism were cut, and these -corner faces increased in size until they met, the resulting octahedron -would be longer (or shorter) from top to bottom than from side to side -or front to back, but the measurement from front to back would be equal -to the one from side to side. In this system we may have the vertical -edges of the prism beveled, and not have to bevel the horizontal ones, -or we may bevel the horizontal edges and not the vertical ones. There is -no dodecahedron in this system or in any other system than the -isometric. The forms in this tetrahedral system are really a combination -of the four sides of the square prism with such modifications as equally -affect them all, with two ends which may be flat, or pyramidal, or -modified pyramidal faces. - - -Orthorhombic system - -The third system has all three axes unequal, but all three are still at -right angles with each other. This is saying that the lines of force in -the crystals are all at right angles to each other but of unequal value. -The faces in this case are all in pairs. What happens at one end of an -axis must happen at the opposite end, but does not need to happen at the -ends of any of the other axes. We are dealing with pairs of faces (one -at either end of an axis), and if three such pairs are combined in the -simplest manner, the resulting figure will be a rectangular prism. If we -cut the eight corners of this prism and enlarge the faces until they -meet, the result is an octahedron, in which the distance from top to -bottom, from side to side, or from front to back is not the same in any -two cases. (See Plate 2.) In this system if a face is made by beveling -one edge of the prism there must be a corresponding face on the edge -diagonally opposite, but there does not have to be one on any of the -other edges. However if a corner is cut, that face affects all the axes -and so all the corners must be cut. A great many crystals occur in this -system, and some of them which are prismatic in shape may give trouble, -for it is not uncommon for the vertical edges of the prism to be so -beveled, that two of the original prism faces are obliterated, and the -two remaining faces added to the four new faces make a six-sided prism, -which at first glance seems to belong to the hexagonal system. (See -Plate 3, fig. 3.) Close examination however will show that, instead of -all the prism faces being alike, as would be necessary for the hexagonal -system, they are really in pairs, and one pair at least will be -distinguished in some way, such as being striated, pitted, or duller. - - -Monoclinic system - -The fourth system has all the axes unequal, the a axis and the b axis at -right angles to each other, but the c axis is inclined to the a axis, -meeting it at some other than a right angle. The monoclinic system is -like the orthorhombic system except that it leans, or is askew, in one -direction. The result is that the faces at the ends of the b axis are -rhombohedral, while the others are rectangular. As in the foregoing -system, the faces are in pairs at opposite ends of the axes; and as in -the orthorhombic system, a face may occur on one edge and only have to -be repeated on the edge diagonally opposite. The simplest form in this -system will be made by combining the three pairs of faces at the -opposite ends of the axes, which gives a prism, which is rectangular in -cross section, but leans backward (or forward) if placed on end. As in -all the systems, if a corner is cut, all must be cut; and if these -corner faces are extended to meet each other, an octahedron results, in -which, as in the prism, no two axes are equal. If this octahedron is -properly orientated (_i.e._ with the a and b axes horizontal), it will -lean forward or backward. Many minerals belong to this system; and, as -in the orthorhombic system, it is not uncommon to have the vertical -edges so beveled that two of the prism faces are obliterated, and the -remaining two prism faces with the four new faces make a six-sided -prism, which seems hexagonal. (See plate 3, figure 3.) However, such a -pseudo-hexagonal prism may be recognized by at least one pair of the -faces having distinguishing marks (striæ, pits, or dullness), instead of -all being just alike. - - -Triclinic system - -The fifth or triclinic system has all the axes unequal, and no two of -them intersect at right angles. As in the two preceding systems the -faces occur in pairs at the opposite ends of the axes. This is the most -difficult system in which to orientate a crystal, but fortunately only a -few crystals occur in this system, such as the feldspars. - - -Hexagonal system - -Lastly there is a group of crystals which have four axes, one vertical, -and three in the horizontal plane which intersect each other at angles -of 60°, all these three being equal to each other, but different from -the vertical axis. The simplest form in this system is the six-sided -prism. If one corner of this prism is cut all must be, and if these -corner faces are extended to meet each other, a double-six-sided pyramid -results. In this system if one of the vertical edges of the prism is -beveled, all must be, but the horizontal edges need not be; or the -horizontal edges may be beveled and the vertical ones not. The ends as -they are related to the c axis may be developed independently of the -prism, and so the prism may be simply truncated by a flat end, or have -pyramids on either end. - - -Hemihedral forms - -In this system it is quite common to have forms which result from the -development of each alternate face of either the prism or the double -pyramid. In the case of the prism, if every alternate face is developed -(and the others omitted) a three-sided prism results, as in tourmaline. -In the case of the double pyramid if the three alternate faces above are -united with the three alternate faces below, a six-sided figure is -formed, which is known as the rhombohedron, as all the faces are -rhombohedral in out-line and all equal. These forms in which only half -the faces are developed are known as hemihedral forms. The same sort of -thing may happen in the isometric system in the case of the octahedron, -and also in the case of the octahedron of other systems. When half the -faces of the octahedron are developed, two above unite with two below -and make a four-sided figure, known as a tetrahedron. (See plate 10.) -While tetrahedrons may occur in any of the first five systems they are -not common outside the isometric system. - - -Twinning - -Another modification of the simple forms which will be met occasionally -is twinning. By this is meant two crystals growing together as though -placed side by side on some one of the faces, and then revolved until -the two axes which would normally be parallel are at some definite angle -with each other, 60°, or 180° which is commoner. The surface of contact -between the two crystals is called the _composition face_, and as no -more material can be added on that face the crystals continue to grow -developing the other faces, and we find faces in contact with each other -which should be at the opposite end or other side of the crystals. This -contact of faces which should not come in contact, and the presence of -reentrant angles are indications of twinning. In some minerals the -twinning may be repeated time and again, and if the twinning is on one -of the end faces a branching structure results, as in frost and snow -crystals, or the multiple twinning may be of crystals growing side by -side when the final form will approximate a series of thin sheets placed -side by side as in some feldspars. The peculiar forms characteristic of -individual minerals are taken up under the respective minerals. - -Other important properties of minerals are hardness, cleavage, specific -gravity, streak, luster, and color. - - -Hardness - -Hardness may be defined as the mineral’s resistance to abrasion or -scratching. It is measured by comparing a mineral with Moh’s scale, a -set of ten minerals arranged in the order of increasing hardness, as -follows: - - 1 talc - 2 gypsum - 3 calcite - 4 fluorite - 5 apatite - 6 feldspar - 7 quartz - 8 topaz - 9 corundum - 10 diamond - -A set for measuring hardness may be purchased from any dealer in mineral -supplies. For rough determination, as in the field, the following -objects have the hardness indicated; the finger nail 2¼, a penny 3, a -knife blade about 5.5, and glass not over 6. In testing, a mineral is -harder than the one it will scratch, and softer than the one by which it -is scratched. For instance, if a mineral will scratch calcite and is -scratched by fluorite, it is between 3 and 4 in hardness, say 3.5. When -two samples mutually scratch each other they are of equal hardness. Care -must be used in determining hardness, especially with the harder -minerals; for often, when testing a mineral, the softer one will leave a -streak of powder on the harder one, which is not a scratch. One should -always rub the mark to make sure it is really a groove made by -scratching. - - -Cleavage - -Cleavage is the tendency, characteristic of most minerals, and due to -the arrangement of their molecules, to cleave or break along definite -planes. The cleavage of any mineral is not irregular or indefinite, but -characteristic for each mineral, and always parallel to possible or -actual faces on the crystal, and always so described. For instance -galena has three cleavages, all equally good, and parallel to the cube -faces; so it is said to have cubic cleavage. In the same way fluorite -has octahedral cleavage, and calcite rhombic cleavage. In some minerals -cleavage is well developed in one plane, and less developed in other -planes, or it may be lacking altogether. The varying degrees of -perfection by which a mineral cleaves are expressed as, perfect or -imperfect, distinct or indistinct, good or poor, etc. - - -Specific gravity - -The specific gravity of a mineral is its weight compared with the weight -of an equal volume of water, and is therefore the expression of how many -times as heavy as water the mineral is. For instance the specific -gravity of pyrite is 5.1, which is saying it is 5.1 times as heavy as -water. In a pure mineral the specific gravity is constant, and an -important factor in making final determinations. As ordinarily obtained, -a piece of pure mineral is weighed in air, which value may be called x. -It is then immersed in water and again weighed, and this value is called -y. The difference between the weight in air and that in water is the -weight of an equal volume of water. Then we have the following formula: - - specific gravity = (x)/(x-y). - -Various balances have been devised for making these measurements, but -any balance which will weigh small objects accurately, may be adapted to -specific gravity work, by hanging a small pan under the regular weighing -pan. When using this balance, care is taken to see that the lower pan is -always submerged in water, even while the mineral is being weighed in -air, so that when weighed in water in the lower pan, the weight of this -lower pan has already been considered. - - -Streak - -By streak is meant the color of the mineral when powdered. For some -minerals, especially metallic ores, it is of great importance, for it -remains constant, though the color of the surface of the mineral changes -materially. It is most readily determined by rubbing a corner of the -mineral on a piece of unglazed porcelain. Small plates, known as “streak -plates” are made for this purpose. - - -Luster - -The luster of a mineral is the appearance of its surface by reflected -light, and it is an important aid in determining many minerals. Two -types of luster are recognized; metallic, the luster of metals, most -sulphides and some oxides, all of which are opaque on their thin edges; -and non-metallic, the luster of minerals which are more or less -transparent on their thin edges, and most of which are light colored. -The common non-metallic lusters are; vitreous, the luster of glass; -resinous, the appearance of resin; greasy, oily appearance; pearly, the -appearance of mother-of-pearl; silky, like silk due to the fibrous -structure; adamantine, brilliant like a diamond; and dull, as is chalk. - - -Color - -When used with caution color is of the utmost importance in determining -minerals, especially in making rapid determinations. In metallic -minerals it is constant and dependable; but in the non-metallic minerals -it may vary, due to the presence of small amounts of impurities which -act as pigments. Color depends on chemical composition, and when not -influenced by impurities is termed _natural_; but when the color is due -to some inclosed impurity it is termed _exotic_. In this latter case -caution must be used in making determinations. Many minerals are -primarily colorless, but take on exotic colors as a result of the -presence of small quantities of impurities; for instance, pure corundum -is colorless, but with a trace of iron oxide present becomes red, and is -called the ruby, or with a trace of cobalt becomes blue and is called -sapphire. - - - - - CHAPTER III - THE MINERALS - - - KEY TO THE MINERALS, BASED ON HARDNESS, COLOR, ETC. - - OPAQUE COLORS - Color Hardness Streak Remarks Mineral - - Red - scarlet 2.5 scarlet surface tarnishes prousite - black - 2.5 vermilion surface scarlet to cinnabar - dark red - ochre 7 white non-crystalline jasper - 6 ochre red color red to hematite - almost black - rose 4 white effervesces in rhodochrosite - warm acid - dark 4 orange zincite - 2.5 purplish red surface tarnishes pyrargyrite - black - brownish 3.5 brownish red cuprite - Orange 3.5 white to pyromorphite - yellowish - 1-1½ orange realgar - Blue 5.5-6 white in igneous rocks sodalite - azure 4 azure azurite - sky 7 & 4.5 white blade-like crystals cyanite - turquoise 6 blue non-crystalline turquois - 2-4 white chrysocolla - Green - malachite 3.5 lighter green malachite - olive 6.5-7 white in igneous rocks olivine - 3.5 white to yellow pyromorphite - 2 white mica-like cleavage chlorite - 1 white greasy feel, color talc - light to dark - olive green - yellowish 6.5 white epidote - 2.5-4 white color yellow green serpentine - to olive - Yellow - golden 2.5 shining non-crystalline gold - brassy 6 greenish-black usually crystalline pyrite - 6 greenish-gray color pale brassy marcasite - yellow, usually - non-crystalline - 5.5 greenish-black colors nitric acid millerite - green - 4 greenish-black color golden chalcopyrite - similar to gold - 3.5 dark brown purplish tarnish tetrahedrite - on surface - bronze 5.5 pale color with coppery niccolite - brownish-black cast - 4 dark gray-black with speedy black pyrrhotite - tarnish - 3 gray-black brownish with bornite - bluish tarnish - 2.5 shining coppery red color copper - sulphur 3.5 white to compact masses pyromorphite - yellowish - 2 yellow sulphur - 1-3 earthy masses carnotite - Brown - violet 1½ shining tarnishes black cerargyrite - yellowish 7.5 white 4-sided prisms zircon - 6.5 gray cassiterite - 5.5 ochre yellow compact to earthy limonite - masses - 5 brownish-yellow goethite - 4.5 black wolframite - 3.5 yellowish-brown sphalerite - 3.5 white siderite - grayish 7.5 white often twinned staurolite - 6.5 pale brown rutile - 3.5 white to earthy masses pyromorphite - yellowish - reddish 7 white dodecahedrons & garnet - trapezohedrons - Black 6.5 gray cassiterite - 6 reddish-brown franklinite - 6 black magnetic magnetite - 5.5 dark brown chromite - 5.5 black yellow precipitate wolframite - in sulphuric acid - 5-6 black non-magnetic ilmenite - 5-6 brownish-black compact masses psilomelane - 5 brownish-yellow surface often goethite - brownish - 3.5 dark brown tetrahedrons tetrahedrite - 2.5 silvery fresh surfaces silver - silver color - 2.5 scarlet fresh surfaces prousite - bright red - 2.5 purplish red fresh surfaces red pyrargyrite - 2 black earthy masses pyrolusite - 1 steel gray greasy feel graphite - Metallic 2.5 black tarnishes black, chalcocite - Gray bluish, or green - 2.5 lead gray sectile argentite - 2.5 lead gray cubic cleavage galena - 2 lead gray long prismatic stibnite - crystals - 1.5 bluish gray in scales molybdenite - steel 5.5 gray black rose color in smaltite - nitric acid - 4.5 steel gray very heavy platinum - 4 reddish black often in striated manganite - prisms - 1 gray with greasy feel graphite - silvery 5.5 black arsenopyrite - 2.5 silvery tarnishes black on silver - exposure - reddish 5.5 gray black rose color in cobaltite - nitric acid - pearly 1-1½ shining exposed surfaces cerargyrite - violet brown - White, with 4 white porcelainous magnesite - impurities masses, - effervesces in acid - grayish 2 white earthy masses, kaolinite - or greasy feel - yellowish - 1-3 white earthy masses bauxite - 1 white greasy feel, talc - fibrous or scaly - - TRANSPARENT OR TRANSLUCENT COLORS - Color Hardness Remarks Mineral - - Colorless or with faint tinges of color due to impurities - 10 in octahedrons diamond - 9 in hexagonal prisms corundum - 8 in hexagonal prisms topaz - 7 in three-sided prisms tourmaline - 7 in hexagonal prisms quartz - 7 non-crystalline chalcedony - 7 or 4.5 cubes with beveled edges boracite - 6 non-crystalline, pearly luster opal - 5.5 rhombohedrons willemite - 5.5 trapezohedrons analcite - 5.5 tufts of needle-like crystals natrolite - 5.5 sheaf-like bundles of crystals stilbite - 5 hexagonal prisms with basal cleavage apatite - 5 effervesces in acid smithsonite - 5 becomes jelly-like in acid calamine - 4.5 monoclinic prisms colemanite - 4 in cubes fluorite - 3.5 effervesces in acid, but one cleavage aragonite - 3.5 effervesces in acid, heavy cerrusite - 3 effervesces in acid, rhomboidal calcite - cleavage - 3 no effervescence, but soluble in anglesite - nitric acid - 2.5 in cubes tastes of salt halite - 2 soluble in water, sweetish taste borax - 2 1 perfect cleavage, and two imperfect gypsum - cleaves at 66 with each other - White or with faint tinges of color due to impurities, such as pink, - bluish, etc. - 7 hexagonal prisms quartz - 7 non-crystalline chalcedony - 7 or 4.5 cubes with beveled edges boracite - 6 non-crystalline, pearly luster opal - 6 cleavage in 3 directions, good in 2 feldspar - and imperfect in the other - 5.5 short eight-sided prisms pyroxene - 5.5 long six-sided prisms amphibole - 5.5 trapezohedrons analcite - 5.5 tufts of needle-like crystals natrolite - 5.5 sheaf-like bundles of crystals stilbite - 5.5 rhombohedrons willemite - 5 effervesces in acid smithsonite - 5 becomes jelly-like in acid calamine - 4.5 & 7 cubes with beveled edges boracite - 4.5 monoclinic prisms colemanite - 4 effervesces in acid, porcelainous magnesite - 3.5-4 effervesces in acid, heavy, red color strontianite - in flame - 3.5 effervesces in acid, heavy, green witherite - color in flame - 3.5 effervesces in warm acid, rhomboidal dolomite - cleavage - 3.5 effervesces in acid, cleavage in one aragonite - direction only - 3.5 effervesces in acid, heavy, does not cerrusite - color flame - 3-3.5 no effervescence, cleavage in three anhydrite - directions at right angles - 3 effervesces in acid, rhomboidal calcite - cleavage - 3 tabular crystals, heavy, green color barite - in flame - 2-3 cleaves in thin elastic sheets mica - 2.5 cleaves in cubes cryolite - 2.5 cubes, soluble in water, salty taste halite - 2 1 perfect cleavage, and 2 less perfect gypsum - ones - 2 cleaves in thin non-elastic sheets chlorite - 2 soluble in water, tastes sweet borax - 1 greasy feel talc - Green 9 hexagonal prisms oriental - emerald - 8 octahedrons spinel - 7.5 hexagonal prisms beryl - 7 three-sided prisms tourmaline - 7 dodecahedrons or trapezohedrons garnet - 7 non-crystalline prase or - plasma - 6.5-7 non-crystalline, olive color olivine - 6.5 yellow green color, rather opaque epidote - 6 non-crystalline, pearly luster opal - 5.5 short eight-sided prisms pyroxene - 5.5 long six-sided prisms amphibole - 5 hexagonal prisms apatite - 4 cubes fluorite - 3.5 effervesces in acid cerrusite - 2.5-4 somewhat greasy feel, massive or serpentine - fibrous - 2 in mica-like scales, non-elastic chlorite - 1 greasy feel, fibrous or scaly talc - Red 9 hexagonal prisms ruby - 8 octahedrons spinel - 7 three-sided prisms tourmaline - 7 dodecahedrons or trapezohedrons garnet - 7 hexagonal rose quartz - 7 non-crystalline jasper or - carnelian - 6 pearly luster fire opal - 4 cubes, rose tints fluorite - 2-3 pink mica-like scales lepidolite - Blue 9 hexagonal prisms sapphire - 7 & 4.5 blade-like crystals cyanite - 6 non-crystalline masses turquois - 5.5-6 in igneous rocks sodalite - 4 azure color azurite - 3.5 effervesces in acid, heavy cerrusite - 2-4 earthy masses, turquoise color chrysocolla - Violet 7 hexagonal prisms amethyst - 4 cubes fluorite - Yellow 9 hexagonal prisms oriental - topaz - 8 octahedrons spinel - 8 hexagonal prisms topaz - 4 cubes fluorite - Brown 9 hexagonal prisms corundum - 8 octahedrons spinel - 7.5 four-sided prisms zircon - 7 hexagonal prisms smoky quartz - 7 three-sided prisms tourmaline - 7 non-crystalline flint - 6 non-crystalline opal - 5.5 short eight-sided prisms pyroxene - 5.5 long six-sided prisms amphibole - 2-3 cleaves into thin sheets mica - Black 9 hexagonal prisms corundum - 8 octahedrons spinel - 7 three-sided prisms tourmaline - 5.5 short eight-sided prisms pyroxene - 5.5 long six-sided prisms amphibole - 2-3 cleaves in thin sheets mica - - - The Gold Group - -Gold was undoubtedly the first metal to be used by primitive man; for, -occurring as it did in the stream beds, its bright color quickly -attracted the eye, and it was so soft, that it was easily worked into -various shapes, which, because they did not tarnish, became permanent -ornaments. The metal is associated with the very earliest civilizations, -being found in such ancient tombs as those at Kertsch in Crimea and in -northern Africa and Asia Minor. It was used in the cloisonné work of -Egypt 3000 years B.C. In America the Indians, especially to the south, -were using it long before the continent was discovered. - -Of all the metals gold is the most malleable, and its ductility is -remarkable, for a piece of a grain’s weight (less than the size of a pin -head) can be drawn out into a wire 500 feet long; and it can be beaten -into a thin leaf as thin as ¹/₂₅₀₀₀₀ of an inch in thickness, and thus a -bit, weighing only a grain, can thus be spread over 56 square inches. - -It forms very few compounds, but has a considerable tendency to make -alloys (_i.e._, mixtures with other metals without the resulting -compound losing its metallic character). In Nature gold is never -entirely pure, but is an alloy, usually with silver, there being from a -fraction of 1% up to 30% of the silver with the gold, the more silver in -the alloy, the paler the color of the gold. Australian gold is the -purest, having but about .3% of silver in it, while Californian gold has -around 10% and Hungarian gold runs as high as 30% of silver. Another -alloy fairly abundant in Nature is that with tellurium, such as -_calaverite_ (AuTe₂) which is a pale brassy yellow, similar to pyrite, -but with the hardness of but 2.5. Another combination includes gold, -silver and tellurium, _sylvanite_, (AuAgTe₄) a silvery white mineral -with a hardness of but 2. Such combinations are known as tellurides and -the calaverite is mined as a source of gold at Cripple Creek, Colo., -while the sylvanite is one of the important ores of gold in South -Africa. Occasionally gold is also found alloyed with platinum, copper, -iron, etc. Jewelers make several alloys, “red gold” being 3 parts gold -and 1 of copper, “green gold” being the same proportions of gold and -silver, and “blue gold” being the combination of gold and iron. Our gold -coins are alloys, nine parts gold and one of copper, to give them -greater durability. Most of the gold recovered from nature is found -native, _i.e._, the pure metal, or with some alloy. - - -Gold -Au -Pl. 5 - -Usually non-crystalline, but occasionally showing cube or octahedral -faces of the isometric system; hardness 2.5; specific gravity 19.3; -color golden yellow; luster metallic; opaque. - -Gold is mostly found as the metal and is readily recognized by its -color, considerable weight, hardness, malleability, and the fact that it -does not tarnish. It usually occurs in quartz veins in fine to thick -threads, scales or grains, and occasionally in larger masses termed -“nuggets.” It is insoluble in most liquids so that when weathered from -its original sites, it was often washed down into stream beds, to be -found later in the sands or gravels, or even in the sea beaches. When -thus found it is termed “placer gold,” and its recovery is placer -mining. Most of the original discoveries of gold have been in these -placer deposits; and from them it has been traced back to the ledges -from which it originally weathered. In the placer deposits the size of -the particles varies from fine “dust” up to large nuggets, the largest -found in California weighing 161 pounds; but the largest one found in -the world was the “Welcome Nugget,” found in Australia, and weighing 248 -pounds. When gold was discovered in California in 1848, this became the -chief source for the world, but later this distinction went to -Australia, and now belongs to South Africa, which today yields over half -the annual supply. - -The ultimate source of gold is from the lighter colored igneous rocks, -like granites, syenites, and diorites, throughout which it is diffused -in quantities too small to be either visible or worth while to extract. -It becomes available only when it has been dissolved out by percolating -waters and segregated in fissures or veins, either in or leading from -these igneous rocks. Generally this transfer of gold has taken place -when the rocks were at high temperatures, and by the aid of water (and -perhaps other solvents) which was also at high temperatures. The -presence of gold in sandstones, limestones, etc., is secondary, as is -also its presence in sea water, in which there is reported to be nearly -a grain (about five cents worth) in every ton of water. Beside the -direct recovery of gold from gold mining, a great deal is obtained from -its association with iron, copper, silver, lead and zinc sulphides, in -which it is included in particles too fine to be visible, but in -quantities large enough to be separated from the other metals after they -are smelted. - -In the United States gold is found in the Cordilleran region from -California to Alaska, in Colorado, Nevada, Arizona, Utah, the Black -Hills of South Dakota, and in small quantities in the metamorphosed -slates of North and South Carolina, Georgia, and in Nova Scotia. - - - The Silver Group - -Though much commoner than gold, silver did not attract the eye of man as -early, probably because it tarnishes when exposed to air or any other -agent having sulphur compounds in it, and a black film of silver -sulphide covers the surface. Its first use was for ornaments, and some -of these found in the ruins of ancient Troy indicate its use as early as -2500 B.C. A thousand years later it was being used to make basins, vases -and other vessels. - -Silver is next to gold in malleability and ductility, so that a grain of -silver can be drawn out into a wire 400 feet long, or beaten into leaves -¹/₁₀₀₀₀₀ of an inch in thickness. As a conductor of electricity it is -unsurpassed, being rated at 100% while copper rates 93%. Silver is also -like gold in the freedom with which it alloys with other metals, such as -gold, copper, iron, platinum, etc. All our silver coins, tableware, -etc., have some copper alloyed with the silver to give it greater -hardness and durability. - -Unlike gold, silver freely enters into compounds with the non-metals, -which is the reason that it is not found primarily in its native state, -but usually as a sulphide. Its ultimate source is in the igneous rocks, -few granites or lavas, on analysis, failing to show at least traces of -silver. Before it is available as an ore, or mineral, it has been -dissolved from the original magma, and segregated in fissures or veins, -along with such minerals, as quartz, fluorite, calcite, etc. This seems -to have taken place while the igneous rocks were still hot, and by the -agency of vapors and liquids which were also hot. The presence of silver -in sedimentary and metamorphic rocks, or even in sea water, is -secondary. - -The primary deposition of silver is usually in the form of sulphides, -the commoner of which are, argentite or silver sulphide, pyrargyrite or -silver and antimony sulphide, and prousite, or silver and arsenic -sulphide. Its occurrence as native silver, or the chloride, cerargyrite, -is secondary and due to the reactions which have taken place when -sulphide deposits have been subjected to weathering agents. - -The United States produces about 25% of the world’s supply, Mexico some -35%. It is especially found along the Cordilleran ranges of both North -and South America. - - -Silver -Ag -Pl. 6 - -Usually non-crystalline, but occasionally showing cube or octahedron -faces of the isometric system; hardness 2.5; specific gravity 10.5; -color silvery white; luster metallic; opaque. - -When found in its native state silver is usually in wirey, flakey, or -mossy masses; but sometimes masses of considerable size occur, the most -famous being an 800 pound nugget found in Peru, and another of 500 -pounds weight found at Konsberg, Norway, and now preserved in -Copenhagen. When exposed to the air the surface soon tarnishes and takes -on a black color which must be scraped off to see the real color. - -Like gold, silver is usually found associated with other metals, like -iron, copper, lead and zinc; and much of the silver recovered is -obtained in connection with the mining, especially of copper and lead. -Some lead ores have so much silver in them that they are better worth -mining for the silver; galena, for instance, under such circumstances -being termed argentiferous galena. Native silver is a secondary mineral, -having been formed by the reduction of some one of its sulphides by -water, carrying various elements which had a greater affinity for the -sulphur. - -Silver is found along with copper in the Lake Superior region, and in -Idaho, Nevada, and California. - - -Argentite -AgS -Pl. 6 -_silver glance_ - -Usually in irregular masses, but sometimes in cubes; hardness 2.5; -specific gravity 7.3; color and streak lead gray; luster metallic; -opaque on thin edges. - -Argentite, the simple sulphide of silver, is the chief source from which -silver is obtained. It looks like galena, and has the same hardness, -streak and specific gravity, but can be distinguished by the galena -having a very perfect cubic cleavage while the argentite has no -cleavage. Argentite is easily cut with a knife (sectile). It is usually -found in irregular masses, but sometimes in cubes which make very choice -cabinet specimens; and is associated with such other minerals as galena, -sphalerite, chalcopyrite, pyrite, fluorite, quartz, and calcite. - -It occurs in fissures and veins all through the Cordilleran regions, -especially in California, Colorado, Nevada (Comstock Lode), Arizona -(Silver King Mine) and about the shores of Lake Superior. - - -Pyrargyrite -Ag₃SbS₃ -Pl. 7 -_ruby silver_ or _dark red silver_ - -Usually occurs in irregular masses; hardness 2.5; specific gravity 5.8; -color dark red to black; streak purplish red; luster metallic to -adamantine; translucent on thin edges. - -Pyrargyrite, the sulphide of silver and antimony, is distinguished by -its dark red color and the purplish streak. It may look like prousite, -but is easily distinguished from the latter which has a scarlet streak. -It also at times looks like hematite and cinnabar, but the hematite has -a hardness of 6, and the latter has the bright red color throughout, -while pyrargyrite turns black when exposed to the light, so that the -characteristic red color will be seen only on fresh surfaces. The -characteristic red color can only be kept on the mineral if it is -constantly protected from the light. - -Sometimes pyrargyrite occurs in crystals and these belong to the -hexagonal system, and are prisms with low faces on the ends, as on plate -7, and the mineral is peculiar in that the faces on the opposite ends -are unlike. - -Pyrargyrite is found mostly in fissures and veins of quartz, fluorite, -calcite, etc., and associated with pyrite, chalcopyrite, galena, etc. It -is fairly common in Colorado in Gunnison and Ouray counties, in Nevada, -New Mexico, Arizona, etc. - - -Prousite -Ag₃ AsS₃ -Pl. 7 -_light red_ -_silver_ - -Usually occurs in irregular masses; hardness 2.5; specific gravity 5.6; -color scarlet to vermilion; streak the same; luster adamantine; -transparent on thin edges. - -In general this mineral is very like pyrargyrite, but has the scarlet -color and streak which are entirely characteristic. It is likely to have -the surface tarnished black, which happens on exposure to light, so that -it is essential to be sure that fresh surfaces are being examined. -Occasionally it is found in crystals, of the same type as the preceding -mineral. It is generally found associated with pyrargyrite. - - -Cerargyrite -AgCl -_horn silver_ - -Usually found in irregular masses or incrustations; hardness 1 to 1½; -specific gravity 5.5; color pearly gray, grayish green to colorless, but -turning violet brown on exposure to light; luster resinous; transparent -on thin edges. - -This mineral is usually found in thin seams or waxy incrustations, but -it may occur in crystals in which case they are cubes. It is very soft -and easily cut with a knife, which with its tendency to turn -violet-brown on exposure to light, makes it easy to identify. -Cerargyrite is a secondary mineral, resulting from the action of -chlorine-bearing water on some one of the sulphides of silver. It is -found in the upper portions of mines, especially those in arid regions. - - - The Copper Group - -After gold the next metal to be utilized was copper. About 4000 B.C. our -early forefathers found that by heating certain rocks, they obtained a -metal which could be pounded, ground and carved into useful shapes. -Curiously enough the rocks which had the copper also had some tin in -them, so that this first-found copper was not pure, but had from five to -ten per cent of tin in it, making the resulting metal harder, and what -we call bronze. It was some thousands of years later before they -distinguished the copper as a pure metal, but it worked and made good -tools. The newly found metal was not as ornamental as gold; but, because -it could be made into tools, it had a tremendous influence on man’s -development. As the bronze tools began to take the place of the stone -implements, the “Age of Bronze” was ushered in. In America the Indians -in the Lake Superior region found native copper weathered out of the -rocks and later mined it, and they too pounded it into knives, axes, -needles, and ornaments, but probably never learned to melt it and mold -their tools. At any rate they were not as far advanced in using this -metal when Columbus landed as were the southern Europeans 6500 years -earlier. Since the use of iron became general, copper has not held such -a dominant place, but it still is “the red metal” which holds the second -most important place. - -It is malleable and ductile, though not equal to gold or silver in these -respects. It is a good conductor of electricity and a very large amount -of copper is used in electrical manufacture, roofing, wire, etc. It -alloys with other metals; ten parts copper and one of tin being bronze, -ten of copper and one of zinc is brass, and copper with aluminum is -aluminum bronze. - -Like silver and gold, copper is widely diffused through the igneous -rocks, but before it is available, it must be leached out by solvents -and concentrated in veins, fissures, or definite parts of the lavas or -granites. The primary ores are those which, while the igneous rock was -still hot, were carried by hot vapors and liquids into the fissures and -there deposited, mostly as sulphides. There is a long list of these, but -in this country, the following are the commoner ones; chalcocite the -sulphide of copper, chalcopyrite the sulphide of copper and iron, -bornite another combination of copper, iron and sulphur, and -tetrahedrite copper and antimony sulphide. When these primary ores are -near enough to the surface to come in contact with waters carrying -oxygen, carbon dioxide or silica in solution, they may give up their -sulphur and take some one of these new elements and we have such forms -as cuprite, the oxide of copper, malachite and azurite, carbonates of -copper, or chrysocolla, the silicate of copper. Native copper is also a -secondary deposit laid down in its present state by a combination of -circumstances which deprived it of its original sulphur. In general -copper mining can not be profitably carried on for ores with anything -less than a half of one percent in them; and the use of such low grade -ores has only been possible for a few years, as the result of inventing -most delicate processes in the smelting. - -The United States produces about a quarter of the world’s supply of -copper, with Chile ranking second with about 17%. - - -Copper -Cu -Pl. 8 - -Usually in irregular masses; hardness 2.5; specific gravity 8.9; color -copper red; luster metallic; opaque. Native copper, easily determined by -its color and hardness, is generally found in irregular grains, sheets, -or masses, on which may sometimes be detected traces of a cube or an -octahedral face, showing that it belongs to the isometric system. The -most famous locality is the Upper Peninsula of Michigan which may be -taken as typical. Here, long before it was known historically, the -Indians found and dug out copper to make knives, awls, and ornaments. - -In this region, beds of lava alternate with sandstones and -conglomerates. The copper was originally in the lavas, but has been -dissolved out, and now fills cracks and gas cavities in the lavas, and -also the spaces between the pebbles of the conglomerate. This locality -has been very famous both because of the quantity mined, and also -because of the strikingly large masses sometimes found. Today but little -of the ore runs above 2 percent copper, and it is mined if it has as -little as ½ of one percent. - -While nowhere near as abundant, native copper occurs in the same way in -cavities and cracks in the trap rocks of New Jersey, and along the south -shore of the Bay of Fundy. It is also known from Oregon, the White River -region of Alaska, and in Arctic Canada. - - -Chalcopyrite -CuFeS₂ -Pl. 8 -_copper pyrites_ or _yellow copper ore_ - -Occurs in crystals of irregular masses; hardness 4; specific gravity -4.2; color bronze yellow; streak greenish black; luster metallic; opaque -on thin edges. - -Chalcopyrite resembles pyrite, but its color is a more golden yellow, -and its surface tarnishes with iridescent colors. Then too the hardness -of chalcopyrite is but 4 as compared with 6 for pyrite. When in crystals -this mineral belongs to the tetrahedral system as the c axis is but .985 -in length as compared with I for the two other axes. This difference is -so little that, to the eye, the octahedron appears to belong to the -isometric system. Chalcopyrite occurs in octahedrons and tetrahedrons -(as on plate 8), the latter being the form where but half of the -octahedral faces are developed. However by far the most frequent mode of -occurrence is in irregular masses. - -This is the most important primary ore of copper, and is widely -distributed, being found either in lavas, or in veins, or in fissures -connected with igneous rocks. Apparently the deposits were made, either -at the time of eruptive disturbances or shortly afterward, from vapors -or hot solutions carrying the copper sulphides (and other sulphides) -from the molten igneous rocks. Chalcopyrite is usually associated with -pyrite, galena, sphalerite and chalcocite, as well as quartz, fluorite -and calcite. It is found in all the New England States, in New York, New -Jersey, Pennsylvania, Maryland, Virginia, North Carolina, Tennessee, -Missouri, and all the Rocky Mountain and Pacific Coast States. - - -Bornite -Cu₃FeS₃ -_purple copper ore_ - -Occurs in granular or compact masses; hardness 3; specific gravity, 5; -color bronze-brown with a bluish tarnish; streak gray-black; luster -metallic; opaque on thin edges. - -Bornite is also known as erubescite, blushing ore, variegated copper, -peacock copper, etc., all of which names refer to the highly iridescent -tarnish which fresh faces soon take on when exposed to the air. Though -usually in masses, it is sometimes found in rough cubes of the isometric -system. In this country it is not abundant enough to be used as an ore, -but is likely to be found with other ores like chalcopyrite or -chalcocite. In the east it has been found at Bristol, Conn., and near -Wilkesbarre, Penn., while in the west it may be expected to occur -wherever other sulphide minerals of copper are found. - - -Chalcocite -Cu₂S -Pl. 9 -_copper glance_ - -Occurs in fine grained compact masses; hardness 2.5; specific gravity -5.7; color dark leaden gray; streak black; luster metallic; opaque on -thin edges. - -Chalcocite is one of the important ores of copper, especially in Arizona -and the Butte District of Montana. It resembles argentite in color and -general appearance, but is readily distinguished by being brittle and -having a tendency to tarnish to bluish or greenish colors on fresh -surfaces. Occasionally it occurs in crystals which are in the -orthorhombic system; but the edges of the prism are so beveled that -there are six sides and the prism resembles a hexagonal prism (see page -16). - -In the Butte, Mont., district, the most important copper region in the -United States, fully 50% of the ore is chalcocite, which is a derivative -of the originally deposited chalcopyrite, the latter having lost its -iron. In the veins of this district chalcopyrite, bournite, -tetrahedrite, and several other copper minerals not described in this -book, occur all together, and with them also gold, silver and arsenic -minerals. The gold amounts to about 2¼ cents per pound of copper, and -the silver is in somewhat less quantity. These veins were first opened -to get the silver ores, which were the more important ones down to a -depth of 200 to 400 feet. Below these depths the copper became much more -important. It was the weathering which had removed a large part of the -copper minerals in the upper levels of the veins, but had left a large -part of the silver. Chalcocite is also important in most of the Utah and -Arizona mines. - -In the east it has been found at Bristol, Simsbury and Cheshire, Conn., -and in the west it is found in all the Cordilleran States. - - -Tetrahedrite -Cu₃SbS₃ -Pl. 9 & 10 -_gray copper ore_ - -Occurs in irregular masses and in tetrahedrons of the isometric system; -hardness 3.5; specific gravity 4.7; streak dark brown; luster metallic; -opaque on thin edges. - -In its crystalline form the tetrahedrite occurs in tetrahedrons, which -generally have faces formed by beveling the edges and by cutting the -corners, as in the two figures of plate 10. Chalcopyrite may also occur -in tetrahedrons, but its golden yellow color is entirely different from -the gray-black of the tetrahedrite. When in masses the hardness and the -streak which is dark brown, are very characteristic. - -In England and Bolivia tetrahedrite is an important ore of copper, but -in this country it is simply a copper mineral which is widely -distributed, and associated with most of the mining enterprises, but is -in no case the important ore. It has been found sparingly through the -New England States, at the Kellogg Mines in Arkansas, and abundantly in -Colorado, Montana, Utah, Arizona, Nevada and New Mexico. - - -Cuprite -Cu₂O -Pl. 9 & 10 -_red copper ore_ - -Occurs in isometric cubes, octahedrons, and dodecahedrons, or in masses; -hardness 3.5; specific gravity 6; color dark brownish-red; streak -brownish-red; luster metallic; translucent on thin edges. - -When in crystals cuprite is easily determined, but when in masses its -fresh surfaces may suggest prousite, but the streak and hardness are -quite different in the two cases. Sometimes its color suggests hematite, -but the latter has the hardness of 6. When found it is often coated with -a thin film of green, which is malachite. - -Except when found as native copper, the ore which contains the greatest -percentage of copper is cuprite with 88.8% of copper. It is likely to -occur in any of the deposits of copper ore, where they are in arid -climates and above the level of the underground water, and is very -frequently associated with malachite and azurite. In the Bisbee, -Arizona, district cuprite is one of the important ores. - -Besides the normal occurrence described above, cuprite may be found in -two other varieties; one where the crystals have grown side by side and -so only the ends have been free for continuous additions of the mineral, -which has resulted in a fibrous mass known as “plush copper ore” or -chalcotrichite; the other an earthy mixture of limonite and cuprite, -which is brick red in color, and termed “tile ore.” - -Cuprite is found sparingly in New England, more abundantly at such -places as Summerville and Flemington, N. J., Cornwall, Penn., in the -Lake Superior region, and fairly abundantly in the Cordilleran States. - - -Malachite -CuCO₃·Cu(OH)₂ -Pl. 11 - -Usually occurs in nodular or incrusting masses; hardness 3.5; specific -gravity 4; color green; streak a lighter green; luster adamantine, silky -or dull; translucent on thin edges. - -The vivid green of malachite is usually enough to determine it at once, -but one may be sure by trying a drop of acid on it, in which case it -effervesces as is characteristic of so many carbonates, but this is the -only carbonate which is vivid green. Generally the malachite is in -irregular masses, but crystals are occasionally found. These are -extremely small and needle-like, and belong to the monoclinic system. In -the Ural Mountains there is a locality where these crystals grow in -fibrous masses, usually radiating from the center. Malachite in such -nodules has a silky luster. These rare nodules have furnished the rulers -of Russia with a unique and much prized material for making royal gifts. -In European museums and palaces one finds many objects carved from this -form of malachite, and marked as gifts of the czars of Russia. - -In the United States malachite is widely distributed, appearing as green -streaks and stains where copper minerals have been exposed to the air. -It is the green tarnish which appears on bronze and copper when exposed -to the weather. It is found in large quantities in New Jersey, -Pennsylvania, Wisconsin, Nevada, Arizona, Utah, New Mexico, etc. The -Bisbee mine in Arizona is the place that has furnished museums with so -many of the handsome specimens of malachite associated with azurite. -These are the most striking specimens for the vividness of their colors -that appear in any collections. - -Malachite has been known since about 4000 B.C., the Egyptians having -mines where they obtained it between the Suez and Mt. Sinai. In those -early days it was particularly a child’s charm, protecting the wearer -from evil spirits. It is still used as a stone of lesser value in making -some sorts of jewelry. - - -Azurite -2CuCO₃·Cu(OH)₂ -Pl. 11 - -Occurs as short prismatic or tabular crystals of the monoclinic system; -hardness 4; specific gravity 3.8; color azure blue; streak lighter blue; -luster vitreous; translucent on thin edges. - -Azurite is another very striking mineral fully characterized by its -color and streak. Like malachite it effervesces in acid. It is very near -to malachite in composition, and by increasing its water content, can -and freely does change to the green mineral; so that few specimens of -azurite are without traces of malachite. It is found in the same places -as malachite, but is not as abundant in the east. - -Azurite with the accompanying malachite is cut and polished to make -semi-precious stones for some forms of jewelry. - - -Chrysocolla -CuSiO₃·2H₂O - -Never occurs in crystals, but in seams and incrustations; hardness 2-4; -specific gravity 2.1; color bluish-green; streak white; luster vitreous; -translucent on thin edges. - -This rather rare mineral often appears in opal- or enamel-like -incrustations, and its color is variable ranging from the typical -bluish-green to sky-blue or even turquoise blue. This is a mineral -resulting from the action of silica bearing waters, coming in contact -with most any of the copper minerals, and is found accompanying cuprite, -malachite, azurite, etc. It is never in large enough quantities to be -used as an ore, but its striking color attracts attention and it can be -found fairly frequently, especially in the west. - - - The Iron Group - -Pure iron is a chemical curiosity which looks very much like silver. As -obtained from its ores, or as it occurs in Nature, iron always has some -impurities with it, such as carbon, silicon, sulphur and phosphorus, and -these are highest in the crudest iron such as “pig-iron.” Its -malleability and ductility are only a little less than for gold and -silver, and so it has a wide range of qualities for use by man. It is -only rarely found native in minute grains in some of the dark lavas. -There is however one remarkable exception to this statement, in that on -Disco Island, Greenland, there is a basaltic rock, from which are -weathered great boulders of native iron up to 20 tons in weight. This -iron is very like that occurring in meteorites, and probably came from -great depths in the earth’s interior. The specific gravity of iron is -7.8. It makes up around 5% of the crust of the earth, and probably -occurs in much larger percentages in the interior of the earth. - -Iron was discovered by man later than gold or silver or copper, about -1000 B.C.; but once found it was so much more abundant than any of these -that it soon dominated over copper, and from Roman times to the present -has been the basis of progress in civilization, and these times are well -called “the iron age.” - -Iron unites freely with the non-metals, and occurs as sulphides, oxides, -carbonates, etc., and is also present as a secondary metal in that great -group of minerals known as the silicates (see page 97). It alloys with a -wide range of other metals, every combination altering the properties of -the iron, and thus making it useful in a still greater range of -manufacture. The introduction of ¼ to 2½% of carbon into iron makes -steel, which is harder (in proportion to the amount of carbon) and -stronger than the pure iron. - -Iron compounds are among the most numerous and important of the colors -in Nature’s paint box, limonite furnishing the browns which color the -soil and so many of the rocks, hematite giving the red color to other -abundant rocks, and magnetite often coloring igneous rocks black, while -the chlorophyll which gives the green color to plants is an iron -compound, as is also the hemoglobin which gives the red to our blood. - -Iron is present in all igneous rocks, and secondarily in the sedimentary -and metamorphic rocks. It is soluble in water, and so is being -constantly transferred from place to place, and changes from one -compound to another, according to the circumstances in which it is -placed. - -The primary forms are pyrite, magnetite and the silicates. When in -weathered rocks the iron is changed to limonite, siderite or hydrated -silicates. Hematite is an intermediate oxide from which the water -contained in limonite has been driven off by moderate heat or bacterial -action. - - -Limonite -2Fe₂O₃·3H₂O -Pl. 12 - -Never crystalline, occurs in mammillary, botryoidal and stalactitic -forms, or in fibrous, compact, oolitic, nodular or earthly masses; -hardness 5.5; specific gravity 3.8; color yellow-brown to black; streak -yellow-brown; luster metallic to dull; opaque. - -Limonite is a very common mineral, the color, streak and hardness -identifying it readily. Iron rust is its most familiar form. When -powdered it is the ochre yellow used in paints. Being so universally -distributed, it is to be expected it will occur in a variety of ways. -First, there is the fibrous type found lining cavities, in geodes, or -hanging in stalactites in caves. This has a silky luster, an opalescent, -glazed or black surface, and is in mammillated or botryoidal masses. -Second, it may occur in compact masses in veins, where it was deposited -by waters; which, circulating through the adjacent rocks, gathered it -from the rocks, and, on reaching the open seams, gave it up again. -Third, it may occur in beds on the bottom of ponds, where it was -deposited by waters which gathered it as they flowed over the surface of -the country rocks. Measurements in Sweden show that it may accumulate in -such places as much as six inches in the course of twenty years. In -ponds and swamps, the decaying vegetation forms organic compounds, which -cause the precipitation of the iron from the water, as it is brought in -by the streams. This sort of iron in the bottom of ponds or swamps is -also known as “bog iron.” Another form in which limonite may occur in -ponds, lakes, or even the sea, is in oolitic masses. In this case the -iron forms in tiny balls, with perhaps a grain of sand at the center, -and one coat of iron after another formed around it, like the layers of -an onion. If the resulting balls are tiny this is called oolitic (like -fish eggs), but if the balls are larger it is pisolitic (like peas). -Bacteria probably have a good deal to do with the precipitation of -limonite in this manner. Fourth, limonite occurs in earthy masses, -usually mixed with impurities like clay and sand, which are the residue -left behind, where limestones have been dissolved by weathering. The -fifth mode of occurrence is known as gossan, or “the iron hat,” which is -a mass of limonite capping a vein of some sulphide mineral, like pyrite, -chalcopyrite or pyrrhotite, which has been exposed to weathering; and in -these minerals the sulphur has been removed, leaving a mass of limonite -over the vein. This is particularly common in the west. Limonite is -quite easily fusible and so was probably the first ore from which early -man extracted iron. - -Limonite is iron oxide, with 3 molecules of water of crystallization (or -constitution) associated with every 2 molecules of the oxide. If -limonite is moderately heated the water is driven out and the resulting -compound is hematite, the same oxide, but without the water. In this -case and many other similar cases, as gypsum, opal, etc., we have two or -more minerals resulting from the presence or absence of water in the -mineral. The water molecules have a definite place in the arrangement of -molecules which determines the structure of the mineral. Sometimes the -water is driven out at a temperature around 212 F., in which case it is -called, water of crystallization, but in other cases as gypsum, a -considerably higher temperature is required to drive out the water, and -then it is called, water of constitution. In all cases the removal of -the water changes the arrangement of molecules and a new mineral -results, with characteristics of its own. - -In this case limonite is only one of a series of minerals which have the -Fe₂O₃ molecule as a basis, and that incorporate more or less water into -their molecular construction as follows: - - Turgite 2Fe₂O₃·H₂O - Goethite Fe₂O₃·H₂O - Limonite 2Fe₂O₃·3H₂O - Xanthosiderite Fe₂O₃·2H₂O - Limonite Fe₂O₃·3H₂O - -Of these goethite is crystalline, the others non-crystalline. They may -occur pure or in all sorts of mixtures, the mixtures usually being -lumped under limonite. The limonite is far the commonest of the series, -goethite is fairly common, but the others are rare as pure minerals. - -Limonite is found in all parts of all states and in every country. -Though so common, it is by no means an important source of iron today, -only about one percent of the iron mined in this country coming from -this source, though in Germany, Sweden and Scotland it is relatively -much more important. - - -Goethite -Fe₂O₃·H₂O -Pl. 12 - -Occurs in lustrous brown to black orthorhombic prisms, usually -terminated by low pyramids; hardness 5; specific gravity 4; color brown -to black; streak brownish-yellow; luster imperfect adamantine; opaque. - -Goethite, named for the poet Goethe, who was interested in mineralogy, -is much less abundant than limonite or hematite, but occurs with them, -when they are in veins. Its usual form is an orthorhombic prism with the -edges beveled, and a low pyramid on either end. The crystals usually -grow in clusters, making a fibrous mass, often radiated, in which case -it is known as “needle iron stone”; or the prisms may be so short as to -be almost scales; when, because of the yellowish-red color, it is called -“ruby mica”. It is found in many states, including Connecticut, -Michigan, Colorado, etc. - - -Hematite -Fe₂O₃ -Pl. 13 & 14 -_specular iron_ - -Occurs in compact, mammillary, botryoidal, or stalactitic masses of dark -red to black color, or in earthy masses of bright to dark red; hardness -6; specific gravity 5.2; color ochre red to black; streak cherry red to -dark red; luster metallic, vitreous, or dull; opaque on thin edges. - -Hematite is readily distinguished from other red minerals by its -hardness and streak. It may occur in crystals, which belong to the -hexagonal system, and are usually hemihedral forms of the double -pyramid, or rhombohedrons. These rhombohedrons usually have the edges -beveled, as in Pl. 13, A; or are tabular in form as a result of the -beveling of two of the opposite edges to such an extent that a form like -Pl. 13 B results. However the usual occurrence is in non-crystalline -masses, which represent transformations from limonite by the loss of -water of crystallization on the part of the limonite. In such cases we -have fibrous, oolitic or compact masses, according to the form in which -the limonite occurred. The transformation from limonite into hematite -involves some heat to drive out the water of crystallization, but -nothing like what is involved in metamorphism. - -Hematite is the source of 90% of the iron mined in this country. Part of -it comes from the famous Clinton iron ore, a layer a foot or more in -thickness; starting in New York State, and extending all down the -Appalachian Mountains to Alabama, where it is ten or more feet thick and -the basis of the Birmingham iron industries. Then there are tremendous -deposits of earthy to compact hematite, probably derived from limonite, -around the west end of Lake Superior. This latter region yields today -around 75% of the iron for this country. - -Loose earthy masses of hematite are often known as “ochre red,” and were -used by the Indians for war paint. Today the same sort of material is -obtained by powdering hematite and using it for red paint. The red color -in great stretches of rock is due to the presence of small amounts of -hematite, acting as cementing material. The red of the ruby, garnet, -spinel, and the pink of feldspars and calcite are due to traces of -hematite. - -This mineral is very common and found in every state. - - -Magnetite -Fe₃O₄ -Pl. 14 -_Magnetic iron ore_ - -Occurs in masses or in isometric octahedrons or dodecahedrons; hardness -6; specific gravity 5.8; color black; streak black; luster metallic; -opaque on thin edges. - -Magnetite is another important ore of iron, and is peculiar in being -strongly magnetic; its name being derived, according to Pliny, from that -of the shepherd Magnes, who found his iron pointed staff attracted by -the mineral when he was wandering on Mount Ida. This magnetic property -has been repeatedly used to locate beds of magnetite, and is very -helpful in separating magnetite from the “black sands,” of which it so -often forms a part. These sands however generally have magnetite with so -much titanium in it that they are unfit for smelting. - -Magnetite is found in association with igneous or metamorphic rocks, and -often represents limonite or hematite which has been altered as the -result of high temperatures. Some of it, in the igneous rocks -especially, was undoubtedly in the molten magma and has crystallized out -from the magma while it was still hot. It is the form of iron always -indicative of former high temperatures. It is an ore mineral for about -3% of the iron in this country, but in Scandinavia and some other -countries, it plays a leading role as the source of iron. - -It is found in the Adirondack Mountains, in New Jersey, Pennsylvania, -Arkansas, North Carolina, New Mexico, and California. - - -Siderite -FeCO₃ -Pl. 13 & 14 -_Spathic iron_ - -Occurs in fibrous botryoidal masses or rhombohedral crystals, sometimes -with curved faces; hardness 3.5; specific gravity 3.8; color gray-brown; -streak white; luster vitreous; translucent on thin edges. - -Like hematite this mineral belongs to the hexagonal system, and -crystallizes in hemihedral form, making the rhombohedron. Its faces are -often curved, which is rare in minerals, only a few forms like this and -dolomite having other than plane faces. When siderite crystals grow in -clusters, the crowding often results in growth on one face only, making -a mass of fibrous character, and in such cases the surface of the mass -is botryoidal in contour. The mineral is likely to oxidize, losing its -gray-brown color, and becoming limonite. In the United States it is -scarcely ever used as an ore for iron, but in Germany and England a -great deal of iron is smelted from this mineral. - -It occurs in Massachusetts, Connecticut, New York, throughout the -Appalachian Mountains, and also in Ohio. - - -Pyrite -FeS₂ -Pl. 15 & 16 -_iron pyrites_ - -Occurs as cubes, octahedrons and pyritohedrons, or in compact masses, -scales or grains; hardness 6; specific gravity 5.1; color brassy yellow; -streak greenish-black; luster metallic; opaque on thin edges. - -This is one of the commonest of all minerals. It is found in all kinds -of rocks, with all kinds of associations, in all parts of the world. Its -crystals are isometric, and cubes and octahedrons are abundant. The -pyritohedron is also a common form, and characteristic of this mineral. -It is a hemihedral form derived from a 24-sided form, _i.e._ the cube -with four faces on each side. On this 24-sided form each alternate face -has developed and the others have disappeared, resulting in a 12-sided -form, known as the pyritohedron, which differs from the dodecahedron in -that each of its faces is five-sided instead of rhomboidal. When in -crystals pyrite can not be easily confused with any other mineral; but -when in masses it is often mistaken for gold, chalcopyrite, pyrrhotite -or marcasite. From the first two, the color should be sufficient to -distinguish it, for they are golden yellow. Pyrrhotite is bronze yellow, -and marcasite is paler yellow. Then too in hardness pyrite is much -harder than any of these minerals except marcasite. This last is the one -which is most likely to cause real difficulty. Its lighter color, and -the fact that it usually comes in fibrous masses are the best -distinctions. - -In spite of being so abundant pyrite is scarcely ever used as an ore for -iron, because the sulphur makes the metal “short,” or brittle, and the -sulphur is not easily gotten entirely out of the iron; but pyrite is -used largely in the manufacture of sulphuric acid, so important to many -of our industries. - -Other sulphides are commonly mixed with pyrite, such as chalcopyrite, -arsenopyrite, argentite, etc.; but the most important impurity is gold, -which is often scattered through the pyrite in invisible particles, and -sometimes in quantities enough to make it worth while to smelt it for -the gold. - -Pyrite is particularly the form in which the sulphur compounds of iron -appear in rocks which have been highly heated, and is to be expected in -metamorphic rocks and also igneous rocks, especially in fissures and -veins leading from the igneous rocks. It may occur in sedimentary rocks, -but in these last it is usually marcasite. - - -Marcasite -FeS₂ -Pl. 15 -_white pyrite_ - -Occurs in orthorhombic crystals, usually grouped to make fibrous or -radiating masses, or non-crystalline in masses; hardness 6; specific -gravity 4.8; color pale brassy-yellow; streak greenish-gray; luster -metallic; opaque on thin edges. - -Marcasite has the same chemical composition, as pyrite, and looks like -it, but is lighter colored and usually occurs in fibrous masses. It is -the commoner form in limestones and shales, while pyrite is more likely -to occur in igneous and metamorphic rocks. It seems probable that -marcasite is due to a more hasty precipitation from cold solutions, -while pyrite is deposited more slowly from hot solutions. - -Isolated crystals of marcasite are rare; but, if formed, they belong to -the orthorhombic system. Usually some form of twinning is present, and -because of the multiple character of the twinning, marcasite crystals -usually show a ragged outline, with reentrant angles. It is most -abundant in radiated masses, which appear fibrous on the broken -surfaces. It decomposes easily, taking oxygen from the air and forming, -even in museum cases, a white efflorescence or “flower,” which is iron -sulphate or melanterite. In moist air it takes water and decomposes to -sulphuric acid which may change the surrounding limestone to gypsum. -Marcasite is found wherever limestones and shales are the country rock. - - -Pyrrhotite -Fe₁₁S₁₂ -_Magnetic pyrites_ - -Occurs in masses; hardness 4; specific gravity 4.6; color bronze; streak -grayish-black; luster metallic; opaque on thin edges. - -Tabular crystals are known, but are very rare. They belong to the -hexagonal system. This form is easily distinguished from the other -yellow minerals by being magnetic. It is by no means as abundant as the -two preceding sulphides of iron, but does occur fairly frequently in -veins in igneous rocks, and less frequently in limestones, large -quantities of sulphuric acid being made from a deposit in limestone at -Ducktown, Tenn. It will be found in most states. When associated with -nickel it is an important source for the latter mineral, as at Sudbury, -Canada. Pyrrhotite is very like a substance found in meteorites, known -as troilite. - - - The Lead Group - -After learning how to get iron from the rocks by rude smelting methods, -the early peoples tried heating various rocks, and some time around 500 -B.C. stumbled upon lead, which is rather easily separated from its ores. -This metal was used through Roman times to make pipes, gutters, etc. - -Lead is a soft metal, fairly malleable, but with little ductility, and -still less tensile strength. Though one of the commoner metals, it does -not occur as pure metal in Nature. It is diffused in minute quantities -through the igneous rocks, and also is found in the sedimentary rocks -and in the sea water. Its minerals are few, galena, the sulphide of -lead, being the commonest, and at the same time the form in which lead -is primarily deposited. Galena may also represent a secondary -deposition. The other minerals, cerrusite, anglesite, and pyromorphite -are results of modification of the galena when it lies near enough to -the surface to be acted on by weathering agents, like water and air. -Lead minerals are usually associated with zinc minerals, there being but -few places where the minerals of the one group occur without the other. -Most lead when first smelted from its ore, contains a greater or less -amount of silver in it, sometimes enough so that the lead ore is better -worth working for the silver than for the lead. - -Lead is used in making pipes, gutters, bullets, etc., and in its oxide -forms in the manufacture of paints and glass. Eighty-three parts of lead -with 17 parts of antimony make type metal. Lead and tin alloy to make -solder. Lead and tin with small amounts of copper, zinc and antimony -make pewter. The United States produce about 20% of the world’s supply -of this metal. - - -Galena -PbS -Pl. 17 -_lead glance_ - -Occurs in cubes or cleavable masses; hardness 2.5; specific gravity 7.5; -color lead-gray; streak lead-gray; luster metallic; opaque. - -While there is quite a group of lead-gray minerals, galena is easily -identified by its cleavage, which is perfect in three directions -parallel to the cube faces. Even a moderate blow of the hammer will -shatter a mass of galena into small cubic pieces. The crystals often -have the corners cut by octahedral faces, and occasionally the edges are -beveled by dodecahedral faces. It is not uncommon to find crystals of -large size, several inches across. If galena has 1 to 2% of bismuth as -an impurity, curiously enough, the cleavage changes to octahedral, but -this is a rare occurrence. - -Galena may occur as a primary mineral in veins associated with igneous -intrusions, or in irregular masses in metamorphic rocks; but it is more -often found in irregular masses in limestones, where the limestone has -been dissolved, and the cavities thus formed, filled with secondary -deposits of galena. It also occurs at the contact between igneous rocks -and the adjacent rock, whatever this may be. Sometimes it is found in -residual clays. - -Among the most important lead deposits are the Cœur d’Alene district in -Idaho, where galena with a high percentage of silver is mined; the -Leadville, Colo., district where lead, silver and gold occur together in -veins; the Joplin, Mo., district, where lead and zinc ores occur -together in irregular masses in limestones; and the Wisconsin district -of similar character. - -When found galena is usually associated with sphalerite, argentite -chalcopyrite, pyrite and calcite. It will be found in every state. - - -Cerrusite -PbCO₃ -Pl. 18 -_White lead ore_ - -Occurs in fibrous or compact masses, or in orthorhombic crystals, -usually on galena; hardness 3.5; specific gravity 6.5; colorless; streak -white; luster adamantine; transparent on thin edges. - -While the crystals of this mineral simulate hexagonal, they are actually -orthorhombic, the simple form being an octahedron with two of its edges -beveled, making double six-sided pyramids (see Pl. 18 A.) Usually prism -faces are present. Twinning is common, both the simple contact sort, as -shown on Plate 18 B, and also the sort in which three crystals have -grown through each other, so as to make a six-rayed crystal. The -considerable weight, and the fact that it effervesces in acid serve to -identify cerrusite. When pure it is colorless, but impurities cause it -to appear white, gray or grayish-black, and sometimes it has a tinge of -blue or green. - -It is likely to occur wherever galena is found, as a secondary mineral -derived from the galena. In this country it is not used as an ore, for, -as in the Leadville district, veins which have cerrusite near the -surface change at moderate depths, and galena takes the place of the -cerrusite. It is found all down the Appalachian Mountains, and in all -the Cordilleran States. Especially fine specimens have come from the -Cœur d’Alene district in Idaho. - - -Anglesite -PbSO₄ -Pl. 18 - -Occurs in grains and masses, or in tabular and prismatic orthorhombic -crystals; hardness 3; specific gravity 6.3; colorless; luster -adamantine; transparent on thin edges. - -Two modes of occurrence are characteristic, one in cavities in galena, -the other in concentric layers around a nucleus of galena. In the former -case fine crystals are developed, in the latter the mineral is in -masses. The crystals look like those of barite, but are soluble in -nitric acid while the barite is insoluble. Sometimes the crystals are -prismatic with pyramidal faces instead of the tabular form. - -It is found in the lead mines associated with galena, and in this -country is not used as an ore for lead, but in Mexico and Australia it -is abundant enough to be mined as an ore. Exposed to water which has -carbon dioxide in it, and most surface waters have some, it readily -changes to cerrusite. It is found in Missouri, Wisconsin, Kansas, -Colorado, and Mexico. - - -Pyromorphite -Pb₅Cl(PO₄)₃ -Pl. 17 -_Green lead ore_ - -Occurs in small barrel-shaped hexagonal crystals, and in fibrous or -earthly masses; hardness 3.5; specific gravity 7; color green to brown; -luster resinous; translucent on thin edges. - -Pyromorphite is found in the upper levels of lead mines, and is formed -by the decomposition of galena. Its green color (sometimes shading off -toward brown), considerable weight and resinous luster, serve to -distinguish this mineral. The crystal form is that of a simple hexagonal -prism, with the ends truncated. It is found in Phœnixville, Penn., -Missouri, Wisconsin, Colorado, New Mexico, etc. - - - The Zinc Group - -Zinc and copper made the brass of early Roman times; but even then, zinc -was not known as a separate metal, the brass being made by smelting -rocks in which both zinc and copper occurred, the zinc never being -isolated until much later. Some time in the later Roman times it seems -to have been obtained separately, but then and all down through the -Middle Ages zinc and bismuth were confused. Our earliest record of zinc -being smelted, as we know it today, was about 1730 in England. In those -earlier days, the product, zinc, or bismuth, or both together, were -known as “spelter,” and this name has clung to zinc in mining and -commercial circles; so that today, if one looks for quotations in the -newspaper, he often finds zinc under the head of spelter. - -Zinc, like lead, is diffused in small quantities through all the igneous -rocks. In places it is segregated in fissures or veins leading from the -igneous rocks, along the contact between igneous rocks and either -sedimentary or metamorphic rocks, in limestones where solution cavities -have been formed and later filled with zinc minerals, and as a residue -where limestones have been weathered away. In all these places it is -closely associated with lead. - -The sulphide, sphalerite, is the primary mineral, and the other -minerals, like zincite, smithsonite, calamine, willemite, franklinite, -etc., are secondary, resulting from modifications of the original -sphalerite. In connection with zinc minerals the region of Franklin -Furnace, N. J., is especially interesting, for at that place are found -two large metamorphosed deposits containing a wide range of zinc -minerals, several of which are not found anywhere else. - -Zinc is soft and malleable, but is only slightly ductile, and has little -tensile strength. It alloys with several metals, and in this form is -most useful today; three parts of copper to one of zinc making brass; -four or more parts of copper and one of zinc, making “gold foil”; copper -and zinc (a little more zinc than copper) making “white metal”; three -parts of copper to one of zinc and one of nickel making German silver; -etc. Zinc is also used in large quantities in galvanizing iron, sheets -of iron being dipped into melted zinc and thus thinly coated. It is also -used in batteries and a wide range of chemical industries. - - -Sphalerite -ZnS -Pl. 19 & 20 -_zinc blende, black jack_ - -Occurs in grains, in fibrous or layered masses, or in isometric -crystals; hardness 3.5; specific gravity 4; color yellow-brown to almost -black; streak light yellow to brownish; luster resinous to adamantine; -translucent on thin edges. - -When in crystals sphalerite occurs most commonly either in dodecahedrons -or in tetrahedrons (hemihedral forms of the isometric octahedron). The -cleavage is fairly good and parallel to the faces of the dodecahedron. -The difficulty usually is to get large enough crystalline masses to see -this cleavage clearly, but by examining the angles between the faces of -cleavage pieces they will be found to be the same as those on a -dodecahedron. When the mineral is pure, it has the color of resin, but -sometimes it is reddish to red-brown, and then it is called “ruby zinc,” -more often it is dark brown due to the presence of iron as an impurity. -This is what the miners call “black-jack.” The presence of iron also -tends to make the streak darker. The hardness, streak and cleavage will -usually determine this mineral readily. - -Sphalerite is the primary ore of zinc and is usually found in fissures -and veins leading from masses of igneous rocks, or along the surface of -contact where igneous rocks like granite or lavas come against such -metamorphic rocks as gneisses, schists, or crystalline limestones. In -the region of Joplin, Mo., however, the sphalerite is of secondary -character, having been gathered by waters circulating through the -limestones, and deposited in them in irregular pockets. This Joplin -district has produced more zinc than any other in the world. The United -States annually produces about 25% of the world’s supply of this metal. - -Sphalerite is always associated with galena, and such other minerals as -argentite, pyrite, chalcopyrite, fluorite, quartz, calcite and barite, -are very apt to be present. It will be found in almost every state, -especially in fissures and veins, and less frequently in cavities in -limestones. - - -Zincite -ZnO -Pl. 19 & 20 -_red zinc ore_ - -Usually occurs massive, but may be found in crystals; hardness 4; -specific gravity 5.6; color deep red; streak orange; luster -subadamantine; translucent on thin edges. - -When in crystals zincite forms in hexagonal prisms with hexagonal -pyramids on the ends. This is rather rare, most of the zincite being -found in massive form. The cleavage is parallel to the prism faces and -perfect. The deep red color and orange streak are wholly characteristic. - -This mineral is so common at Franklin Furnace, N. J., as to be an -important ore, but it is very seldom found elsewhere. This district, as -mentioned before, is a peculiar one for zinc minerals. The zinc beds are -in a metamorphosed limestone, and into this are intruded numerous dikes -of granite. Probably the zinc was originally present in the bed of -limestone as smithsonite, calamine and other secondary minerals of zinc. -When intruded by the hot granite the smithsonite (carbonate) may well -have been altered to the oxide, zincite; while the calamine (hydrous -silicate) became the simple silicate, willemite. - - -Willemite -ZnSiO₄ -Pl. 20 - -Occurs in masses or in crystals; hardness 5.5; specific gravity 4.1; -color pale yellow when pure; luster resinous; translucent on thin edges. - -Willemite is another of the minerals which are distinctively -characteristic of Franklin Furnace, and found elsewhere very rarely. It -is so common there as to be one of the principal ores, and mostly occurs -in irregular masses, but is also found in crystals. These are hexagonal -prisms, with a three-sided (rhombohedral) pyramid on the ends. The color -when pure is whitish or greenish-yellow, but with small amounts of -impurities it may be flesh-red, grayish-white or yellowish-brown. When -in crystals it is easily determined; but when massive it looks like -calamine, and can only be distinguished by placing a bit of the mineral -in a closed tube and heating it, in which case calamine will give off -water vapor, while willemite will not. - -This mineral is one of those resulting from metamorphic alteration and -is derived from calamine, when the latter loses its water of -crystallization. It is common at Franklin Furnace, N. J., and also found -occasionally elsewhere, as at Salida, Colo., and in Socorro Co., New -Mexico. - - -Calamine -Zn₂(OH)₂·SiO₃ - -Occurs as crystalline linings in cavities, or as botryoidal or -stalactitic masses; hardness 5; specific gravity 3.4; colorless to -white; luster vitreous. - -Calamine resembles both smithsonite and willemite when in -non-crystalline masses. From the smithsonite it is easily separated by -the fact that in nitric acid the smithsonite effervesces and the -calamine does not. From willemite it is harder to distinguish, but a -piece may be placed in a closed tube and heated. If it is calamine water -vapor will be given off, if willemite nothing happens. When calamine -occurs in crystals these are orthorhombic and mostly tabular, and the -crystals are peculiar in that the two ends are terminated differently. - -Both this and smithsonite are secondary minerals and usually occur -together when zinc is found in limestones. It is abundant at Franklin -Furnace and Sterling Hill, N. J., and also found at Phœnixville, Penn., -in Wythe Co., Va., and Granby, Mo. - - -Smithsonite -ZnCO₃ -Pl. 21 -_Dry bone_ - -Usually occurs as incrustations, grains, earthy or compact masses, and -as crystals; hardness 5; specific gravity 4.4; color white, yellow, -greenish or bluish; streak white; luster vitreous; transparent on thin -edges. - -When pure this mineral is colorless, but, as it occurs, it is usually -white, or tinged with some shade of yellow, green, or blue, but in all -cases its streak is white. The crystals are rhombohedrons often with -edges beveled or corners cut by other faces. It resembles calamine and -willemite, but is readily separated from either of these by the acid -test, for smithsonite effervesces when acid is placed on it. - -Next to sphalerite, smithsonite is the commonest of the zinc minerals. -It is a secondary mineral, resulting from the action of lime-charged -water acting on sphalerite, and so is likely to be found wherever zinc -minerals occur in a limestone region. In the Wisconsin-Illinois-Iowa -district it serves as a minor ore of zinc, and is termed here “dry -bone.” It is also found in the Missouri and Arkansas districts, and in -Europe is an important ore for zinc. - - -Franklinite -(ZnMn)Fe₂O₄ -Pl. 21 - -Occurs in compact grains or masses, and in isometric octahedrons; -hardness 6; specific gravity 5; color black; streak reddish-brown; -luster metallic; opaque on thin edges. - -This is a mineral peculiar to the Franklin Furnace region, from which it -gets its name. It looks like magnetite, but its reddish-brown streak and -lack of magnetism distinguish it. When it occurs in octahedrons, the -edges are rounded, while those of magnetite are sharp. It is a complex -and variable oxide of zinc, iron and manganese, which has resulted from -the metamorphism of the beds in which it occurred probably being -originally something quite different. - - - The Manganese Group - -Though manganese was known in the mineral pyrolusite in early times, it -was then thought to be magnetite or magnetic iron ore. It was not until -1774 that it was isolated and recognized as a distinct element. - -Manganese is one of the lesser elements in the crust of the earth, -making less than .07 of one percent, but as an alloy with other metals, -especially iron, it has attained a considerable importance to man. It is -used chiefly with iron, 20% of manganese making the alloy, spiegeleisen, -a combination which occurs in Nature in Germany, and from 20% to 80% -making ferromanganese. These alloys are in great demand because they -make an especially tough steel essential in the manufacture of -munitions. The sources for manganese are the oxide ores, manganite, -pyrolusite and psilomelane, which have been formed as secondary -minerals, as a result of the weathering of silicates which carry -manganese. They occur widely enough, but throughout the United States -the deposits are small, and this is one of the elements in which this -country is not self-sufficient. The largest producer of manganese is -Russia; however she consumes almost all of her output at home, and our -supply comes from the next largest producers, India, the Union of South -Africa, and the Gold Coast. A shift in trade may be expected when -Brazil’s recently discovered ore body in Matto Grosso is brought into -full production. Besides being used as an alloy, manganese is employed -in making paints and dyes, for clearing glass, and for some types of -electric batteries. - - -Pyrolusite -MnO₂ - -Occurs in earthy or fibrous masses; hardness 1-2; specific gravity 4.8; -color black; streak black; luster dull; opaque. - -Pyrolusite occurs in soft masses and incrustations, usually leaving a -sooty mark on the fingers. Sometimes it seems to be in crystals, but -these are pseudomorphs which have the form of manganite, from which the -pyrolusite has formed as a result of the water having been driven from -the manganite. Frequently pyromorphite and manganite will be found -together, and in some cases the outer part of a mass or crystal will be -pyrolusite, while the center is still manganite. Psilomelane is another -oxide of manganese with water and may appear very like pyrolusite, but -both manganite and psilomelane have much greater hardness than does -pyrolusite. If there is difficulty in deciding about pyrolusite, it may -be placed in a closed tube and heated. It will not be affected by the -heat, while, under the same circumstances, both manganite and -psilomelane will give off water vapor. - -Pyrolusite usually occurs in black streaks or pockets in residual clays -which have formed as a result of the decomposition of limestones. It may -also occur in dendritic forms in seams and crevices (see manganite). It -is found in Vermont, Massachusetts, Virginia, Arkansas, Colorado, -California, etc. - - -Psilomelane -MnO₂·H₂O - -Occurs in compact botryoidal or stalactitic masses; hardness 5-6; -specific gravity 4.2; color black; streak brownish-black; luster -metallic; opaque on thin edges. - -Psilomelane is very like pyrolusite, and often occurs with it. It is -distinguished by its greater hardness, and the fact, that when heated in -a closed tube, it gives off water vapor. From manganite it is more -easily distinguished, for it never occurs in crystals, while the -manganite is usually crystalline. This and pyrolusite are the principal -ores of manganese. - -Wad is an impure form of psilomelane, having some iron oxide mixed with -the manganese oxide, usually limonite; or the impurity may take the form -of a copper, cobalt, lithium or barium oxide. - -Psilomelane is found at Brandon, Vt., in Arkansas, Colorado, California, -etc. - - -Manganite -Mn₂O₃·H₂O -Pl. 22 - -Occurs in prismatic crystals, or in columnar or fibrous masses; hardness -4; specific gravity 4.4; color steel gray; streak reddish-black; luster -submetallic; opaque on thin edges. - -This is the form taken by manganese oxide when it crystallizes in the -presence of moisture, and pyrolusite frequently changes to manganite -when exposed to moisture. The crystals are orthorhombic prisms, with -striated sides and the ends truncated. These prisms usually occur in -bundles and give the mineral a fibrous appearance. Manganite is not hard -to identify, the striations on the crystals and the streak being very -characteristic. - -In seams and tiny crevices this mineral, and often pyrolusite, grows in -a branching manner, resembling tree-like or “mossy” masses. This is -termed dendritic, and the growths of manganese minerals are called -dendrites. One of the most curious of these is when the “mossy” growth -is inclosed in chalcedony, making the so-called _moss agate_. These moss -agates are abundant through the Rocky Mountains and are frequently cut -for semi-precious stones. The finest ones however come from India and -China. - -Manganite is found in the Lake Superior region, Colorado, etc. - - -Rhodochrosite -MnCO₃ - -Occurs in compact cleavable masses; hardness 4; specific gravity 3.5; -color rose to dark red; streak white; luster vitreous; translucent on -thin edges. - -This usually occurs in pink to red masses which cleave readily parallel -to the faces of the rhombohedron. When it is found in crystals, which -are rare, these too are rhombohedrons. It is usually found in veins as a -gangue mineral with copper, silver or zinc ores. Its beautiful color and -the fact that it effervesces in acid serve to distinguish this mineral. -It is found at Branchville, Conn., at Franklin Furnace, N. J., and in -veins with silver in Colorado, Nevada, and Montana. - - - The Aluminum Group - -Though aluminum is one of the most abundant of all the metals, making -some 8% of the crust of the earth, its union with other elements is so -firm, that only recently have methods been found for getting the metal -free. It was first isolated in 1846, but up to 1890 the extraction of -aluminum was so expensive, that it could not be widely used. About that -time electrical processes were applied to its extraction, and since then -the price has steadily dropped, until now it is under $.20 per pound. It -is very malleable, and ductile, and has high tensile strength. Exposed -to the air, water or ordinary gases, it does not tarnish; and it is very -light, an equal bulk weighing about a third as much as iron. The -combination of lightness and strength, and the fact that it is a good -conductor of electricity, have made it available for a wide range of -uses, such as electrical apparatus, delicate instruments, boats, -aeroplanes, and domestic utensils. - -It is an essential component of all the important rocks, except -sandstone and limestone, and combines to a greater or less degree in a -host of minerals. Though present in clays, shales, argillites, -feldspars, and micas, it is only from bauxite that it has been -successfully extracted. Aside from the small number of simple compounds -of aluminum grouped here, it also takes a part in the make-up of a large -series of minerals termed silicates, treated a little further on in this -book. - -It alloys with other metals, especially copper. The union of copper and -a small amount of aluminum makes aluminum-bronze, which looks like gold -and is used for watch chains, pencil-cases, etc., and also for the -antifriction bearings of heavy machinery. A small amount added to steel -prevents air holes and cracks in casting. - - -Corundum -Al₂O₃ -Pl. 23 - -Occurs in cleavable masses or in hexagonal crystals; hardness 9; -specific gravity 4; colorless, red, yellow, blue, or gray; luster -vitreous to adamantine; translucent to transparent on thin edges. - -Corundum is readily recognized by its hardness, second only to that of -the diamond. The crystals may be simple six-sided prisms, hexagonal -pyramids or combinations of the two. The cleavage is usually described -as parting, for it is by no means perfect, but when it is recognizable -it is parallel to the faces of a rhombohedron, and cleavage pieces may -appear almost cubic. - -When in clear and perfect crystals this mineral is one of the most -highly prized of all the gems. Clear and colorless it is known as the -“_Oriental white sapphire_”; when tinged with blue it is the _sapphire_; -when colored yellow, the “_Oriental topaz_”; when green, the “_Oriental -emerald_”; when purple, the “_Oriental amethyst_” and when red, the -_ruby_. Sapphires range from colorless to deep blue, the value depending -on the shade of the blue, and increasing as the color deepens. The -Oriental topaz can easily be confused with the true topaz, which is a -much commoner and less valuable gem, but can be distinguished by the -hardness, topaz having a hardness of but 8. The name emerald is applied -to several green gems, mostly to beryl, which is not so hard and is the -true emerald. The Oriental emeralds have a value about the same as -diamonds. Rubies of clear and deep color are the rarest of all gems, -ranging in value about three times as high as diamonds of equal size. -The most sought-for shade is the so-called “pigeon-blood red,” and the -value of a stone of this sort is almost dependent on the whim of the -buyer. The best of the rubies come from granites or metamorphosed -limestones in Burma; the best sapphires from Ceylon, though both of -these, and some of the other corundums of gem quality, have been found -in North Carolina and Montana. - -Around these stones, which have been used so long among the Hindus, -Persians, Jews, Egyptians, and Christians, a wealth of lore has been -woven. The sapphire was Saturn’s stone, and a talisman to attract Divine -favor. Where tradition makes the stone on which the ten commandments -were written the sapphire, it is probable that, what was really meant, -is lapis lazuli, as is also the case when sapphires are mentioned as -building stones for the celestial gates. The ruby in ancient lore is -termed “lord of stones,” “gem of gems” etc., and so protected its wearer -that he was safe from injury in peace or war. - -When corundum is colored brown by impurities of iron, it is termed -_corundum_, when black by greater quantities of iron, it is _emery_. -These varieties are far the commonest form in which corundum occurs, and -when ground to finer or coarser powder make the commercial emery. Emery -is likely to be found in sands, making so-called “black sands,” where it -has accumulated as a result of the weathering to bits corundum-bearing -rocks. In some one of its forms, corundum is found in Massachusetts, -Connecticut, New York, New Jersey, and all down the Appalachian -Mountains, also in Colorado, Montana, California, etc. - - -Bauxite -Al₂O₃·2H₂O - -Occurs in grains, or oolitic or clay-like masses; hardness 1-3; specific -gravity 2.5; color white to yellowish-white or reddish-brown. - -Bauxite never comes in crystals, but is usually in earthy masses, which -have resulted from the decomposition of granitic or volcanic rocks, in -circumstances where hot alkaline waters were present. This explanation -seems to apply especially to the deposits in France, which were first -the chief source of the bauxite, and may be applicable to those in -Georgia and Alabama. Some of the other deposits, however, do not seem to -have had any hot water available, and the deposit appears more like -simple decomposition of the underlying rocks by alkaline waters. - -In many cases bauxite resembles limonite in being a mixture of two or -more aluminum oxides with water of crystallization, such as Al₂O₃·H₂O, -Al₂O₃·2H₂O and Al₂O₃·3H₂O. This is particularly true of the bauxite -which resulted from the decomposition of rocks by surface water. - -Bauxite is the ore from which aluminum is obtained. The deposits are not -large, but the United States has its share of them. It is found in -Alabama, Arkansas, Georgia, Missouri, Tennessee, and California. - - -Cryolite -Na₃AlF₆ -_Ice stone_ - -Occurs in pseudo-cubic crystals or massive; hardness 2.5; specific -gravity 3; color white; luster vitreous; transparent on thin edges. - -Cryolite is a relatively soft mineral, colorless to white as snow; for -which reason, and partly also because it comes mostly from Greenland it -is called “ice stone.” It is really monoclinic but the inclination of -the c axis is so slight, that, unless examined carefully, the crystals -appear to be cubic. Until about 1900 great quantities of this mineral -were shipped from West Greenland, and from them the metal aluminum was -extracted. When bauxite was discovered, it was found to be considerably -cheaper to make the aluminum from that mineral, and now cryolite is no -longer sought. Aside from its occurrence in Greenland some cryolite is -found in Colorado, near Pike’s Peak. - - - The Arsenic Group - -The metal, arsenic, is a dark steel gray in color, when the surface is -fresh, but it soon tarnishes. It is very brittle and easily powdered -under the hammer, and its only use as a metal, is for an alloy with lead -in making shot. Its compounds find a wider use. The white powder called -“arsenic” is arsenous acid, and is used mostly in making poisons, which -fortunately are easily detected in animal tissues. Copper arsenate, -(_Scheele’s green_) is a pigment used in making green paint, and -formerly in the green colors of wall paper. A combination of arsenous -acid, copper oxide and acetic acid is the well known _Paris Green_, so -much used for an insecticide. Beside these uses, arsenic serves a large -number of other purposes, as in making glass and enamel, embalming -fluids, and various medicines. - -Curiously arsenic plays a double part, acting part of the time as a -metal, as in the two following minerals, and part of the time as a -non-metal, as in cobaltite, niccolite, etc. - - -Arsenopyrite -FeAsS -Pl. 24 - -Occurs in well formed crystals, grains, or masses; hardness 5.5; -specific gravity 6; color silver-white; streak black; luster metallic; -opaque on thin edges. - -When in crystals, they are usually short prisms of the orthorhombic -system, either end being terminated with a low roof. Though usually -described as silver-white in color, there is always a brassy cast to the -color. Its appearance is much like cobaltite and smaltite, but it can be -easily distinguished from both these by putting a piece in nitric acid. -The arsenopyrite will not materially change the color of the fluid, but -the other two turn it rose-red, and all give off the smell of sulphur. -It looks sometimes like marcasite, but that is yellower, and has the -fibrous structure, not found in arsenopyrite. - -It is found in veins or in metamorphic rocks, associated with argentite, -galena, sphalerite, chalcopyrite and pyrite. It is distinctly a mineral -formed by deposition from hot vapors or hot water rising from either -lavas, or in the course of metamorphism. - -It is found in New Hampshire, Vermont, Massachusetts, Connecticut, New -York, New Jersey, California, etc. - - -Realgar -AsS -Pl. 24 - -Occurs in incrustations or scattered grains; hardness 1.5 to 2; specific -gravity 3.5; color orange; streak orange; luster resinous; opaque on -thin edges. - -Crystals are very rare, but when found are short monoclinic prisms. The -color is aurora-red, changing to orange as soon as it is exposed to the -air. This and the streak are entirely characteristic. It is a mineral -associated with hot vapors or hot waters, and is found about volcanoes, -as deposits from the hot water of the geysers in Norris Basin, -Yellowstone Park, and in veins, associated with barite, stibnite, -quartz, etc., as in Massachusetts, Utah, California, etc. - - -Orpiment -As₂S₃ - -Occurs as incrustations or powdery masses; hardness 1 to 2; specific -gravity 3.5; color lemon yellow; streak yellow; luster resinous. - -This mineral is very like realgar in its physical properties, and likely -to occur with it. It gives the lemon yellow color to the basins about -hot springs, as in the Yellowstone Park, and about volcanoes. It also -comes in veins with realgar. - - - Molybdenum - -Molybdenum is a rare metal, silvery-white in color, brittle and very -difficult to fuse. It is used mostly as an alloy of steel, to make -certain grades of tool steel. The world’s greatest supply is obtained -from Climax, Colorado, where the principal ore mineral is molybdenite. - - -Molybdenite -MoS₂ - -Occurs in scales or scaly masses, occasionally in tabular hexagonal -crystals; hardness 1.5; specific gravity 4.7; color lead-gray; streak -bluish-gray; luster metallic; opaque. - -This mineral is the chief source for the metal molybdenum. Its extreme -softness and greasy feel will distinguish it at once from any other -mineral except graphite, which has much the same qualities, but its -scaly character and the more bluish tinge in streak and color will -distinguish these two. - -It occurs in granites, gneisses, and metamorphic rocks in Colorado, New -Mexico, Maine, Connecticut, New Hampshire, New York, Pennsylvania, etc. - - - Antimony - -Antimony is another hard, brittle metal, of bluish-white color. Exposed -to the air at ordinary temperatures it does not tarnish; and this -combined with its hardness make it useful for such alloys as Britannia -metal, type metal, and pewter. Only one of its minerals, stibnite, is -common enough for mention. - - -Stibnite -Sb₂S₃ -Pl. 25 -_gray antimony_ - -Occurs in prismatic or needle-like crystals; hardness 2; specific -gravity 4.5; color lead-gray; streak lead-gray; luster metallic; opaque. - -The crystals of stibnite are orthorhombic and usually elongated, the -sides striated and the ends with low pyramids on them. Sometimes the -long crystals are curved or even twisted. There is a well-developed -cleavage parallel to face b in the figure. While the color is similar to -that of galena, the form and cleavage are so different that stibnite is -easily determined. - -The ancients used stibnite to color their eyebrows, now it is the source -for the metal antimony. Hungary and Japan are famous for the fine large -crystals they produce; but moderate sized crystals may be found in this -country. It occurs in veins along with pyrite, galena, cinnabar, and -realgar, with quartz, calcite or barite as gangue minerals. - -Stibnite has been found in Arkansas, California, Nevada, and Utah. - - - The Nickel Group - -Nickel as a metal is silvery-white in color, rather hard, and does not -tarnish when exposed to the air. When pure it is malleable and fairly -ductile. It is highly useful for plating other metals to protect their -surfaces. Alloyed with steel, it makes a product of extreme hardness. -Copper, zinc, and nickel make the well known German silver. - -Nickel has a fairly large range of minerals, but they do not occur with -any abundance in the United States, so that we have to import most all -of our nickel. In the earlier days New Caledonia produced most of the -world’s supply, but recently since the finding of large nickel deposits -near Sudbury, Canada, this locality has not only outstripped New -Caledonia, but now produces four-fifths of the world’s supply. In this -country but two nickel minerals will be found at all common. - - -Niccolite -NiAs -Pl. 25 -_copper nickel_ - -Occurs in masses; hardness 5.5; specific gravity 7.4; color pale -coppery-yellow; streak pale brownish-black; luster metallic; opaque on -thin edges. - -Niccolite is very seldom in crystals, but if they do occur they are -hexagonal. The mineral looks a little like smaltite, but in case there -is any question of the determination, dissolve a piece in nitric acid, -and if niccolite, it will color the solution green. - -Niccolite is usually associated with copper and silver ores, and in this -country has been found at Chatham, Conn., and Silver Cliff, Colo. It may -be associated with pentlandite, a sulphide of iron and nickel, which is -similar in appearance, but not so hard, and occurs in small grains -throughout dark lavas. The particles of pentlandite are however so -small, that they are seldom noticeable, but at Sudbury, Canada, this is -the chief ore of nickel. - - -Millerite -NiS -_capillary pyrites_ - -Occurs in needle-like or fibrous crystals; hardness 3.5; specific -gravity 5.5; color brass-yellow; streak greenish black; luster metallic; -opaque on thin edges. - -The fibrous crystals of millerite belong to the orthorhombic system. The -color and streak suggest pyrite, but the crystals are long and slender, -while pyrite is in cubes, octahedrons, etc. If there is any doubt of the -identity of this form, place a piece in nitric acid, and if it is -millerite, it will color the acid green. - -It may occur in veins associated with cobalt and silver minerals, or as -a secondary mineral as at Gap Mine, Penn., or in cavities in sedimentary -rocks. In the last case it usually is in needle-like crystals growing -through calcite crystals, as at St. Louis, Mo., Keokuk, Iowa, and -Antwerp, N. Y. - - - The Cobalt Group - -As a metal, cobalt is hard, brittle, and of a grayish color, tinged with -red. It was not recognized as a separate element until 1735, and even -today is one of the minor metals. Cobalt, chromium and a little tungsten -make the alloy stellite, which has come into large use in making -high-speed tools. The oxide of cobalt (CoO) is “smalt,” used to give the -blue color to porcelain, pottery, glass, tiles, etc. Invisible ink is -made by diluting cobalt chloride in a large quantity of water. This -solution is a faint pink color and practically invisible on paper, but -if heated it loses water and turns blue in color, and is perfectly -visible. - -Cobalt is another of the metals, of which the United States does not -have an adequate supply. Sweden, Norway and India were the chief sources -of supply until cobalt was found near the town of Cobalt in Ontario, -Canada, and now this district furnishes 90% of the world’s supply. - - -Cobaltite -CoAsS -Pl. 26 -_cobalt glance_ - -Usually crystalline in cubes, pyritohedrons or octahedrons; hardness -5.5; specific gravity 6.1; color reddish silver-white; streak -grayish-black; luster metallic; opaque on thin edges. - -In color cobaltite may appear very like arsenopyrite, especially if the -reddish tinge is not strong, in which case the mineral can be definitely -determined by putting a piece in nitric acid. If it is cobaltite the -solution will be colored rose-red, if arsenopyrite there will be no -change of color. The forms of the crystals are the same as those of -pyrite, but the color will easily distinguish cobaltite from pyrite. -This pink color is characteristically present either in or about cobalt -minerals, being sometimes called “cobalt bloom.” It is a -cobalt-arsenic-oxide with water of crystallization (Co₃As₂O₈·8H₂O), -which results from the exposure of cobalt and arsenic minerals to air -and moisture. It is the pink color on the figures of both cobaltite and -smaltite. In Sweden, Norway and India, this is the chief ore for cobalt, -but in the United States it is rather rare, but is found in Oregon, and -at Cobalt, Canada. - - -Smaltite -(CoNi)As₂ -Pl. 26 -_gray cobalt ore_ - -Usually occurs in masses; hardness 5.5; specific gravity 6.2; color -tin-white to steel-gray; streak grayish-black; luster metallic; opaque -on thin edges. - -While very like cobaltite, smaltite is almost never found in crystals, -but when crystals are found, they are cubes. The color is tin-white but -there is usually a pink tinge visible due to the presence of small -amounts of “cobalt bloom.” If in any doubt about the determination of -this mineral, put a piece in nitric acid. If it colors the acid -rose-pink, and is non-crystalline it is pretty surely smaltite; if the -acid is not affected it is arsenopyrite. - -Smaltite is found in Kentucky, Missouri, Colorado, Idaho, California, -and at Cobalt in Canada. - - - Chromium - -This metal gets its name in recognition of the many colors (_chroma_ -“color”), in which its compounds appear. Chromic oxide is a vivid green, -used to color porcelains, pottery, tiles, etc., and also as a substitute -for the arsenical greens formerly used in wall-paper. The chromate of -lead is the pigment, well known to artists as “chrome yellow,” and the -bichromate of potassium is bright red. The metal is obtained in at least -two different forms; one hard, brittle and so resistant to heat as to be -infusible at temperatures which would volatilize platinum; the other as -a powder which burns brightly if heated in air. While used in paints, -dyes, etc., its greatest importance is for the making of ferro-chrome -steel, which is used where resistance to sudden shock is required, as in -armor plate, automobile springs, ball bearings, etc. With tungsten and -cobalt it makes the alloy, stellite, as noted above. - -Chromium was used in relatively small quantities before the first world -war, and we imported our supplies from Turkey, India, New Caledonia, and -Rhodesia. During the last war we started a large-scale development of -low-grade ores in Montana, and can now supply all of our needs from this -source. - - -Chromite -FeCr₂O₄ -_chromic iron_ - -Occurs in grains, masses, or isometric octahedrons; hardness 5.5; -specific gravity 4.4; color black; streak dark-brown; luster -submetallic; opaque on thin edges. - -In form, color and streak chromite resembles magnetite and franklinite. -From the magnetite it is distinguished by being non-magnetic; from the -franklinite, by being insoluble in hydrochloric acid, while the -franklinite is soluble. Chromite furnishes practically all the chromium -used in the arts and manufactures. It is a mineral associated with high -temperatures, and therefore found in dark lavas, serpentine, and -olivine. It occurs in Pennsylvania, Maryland, New Jersey, Montana, -Oregon, Wyoming, and California. - - - Tungsten - -This element is obtained either as a heavy dark-gray metal, which is -very hard and difficult to fuse, or as a dark-gray powder. It is used as -an alloy with iron, one part of tungsten to nine of steel, to make the -ferrotungsten, which has extraordinary hardness, and is used mostly for -high-speed tools. Tungsten is also one of the three metals (cobalt, -chromium and tungsten) which are alloyed together to make stellite. Some -of the tungsten supply is also used to make the films in incandescent -lamps, and in some of the chemical industries. It has but one important -ore, wolframite, and this is found in the United States in but small -quantities; so that we ordinarily have to import the greater part of -what we use. During the last war, under the stimulus of high prices and -the urge of necessity, we did find and produce substantial quantities of -tungsten. China is the world’s largest producer of tungsten ore with -Burma second, and the United States a poor third. - - -Wolframite -(FeMn)WO₄ - -Occurs in monoclinic crystals or in crystalline masses; hardness 5.5; -specific gravity 7.4; color dark-brown to black; streak nearly black; -luster submetallic; opaque on thin edges. - -If in crystals the form will serve to distinguish this mineral from -cassiterite and ilmenite, the two which it most resembles; but if it is -massive the only sure way to decide is to put a piece in strong -sulphuric acid; if it dissolves and throws down a yellow precipitate -(tungstic acid) it is wolframite. - -Like the two other minerals mentioned above it occurs in veins in -igneous rocks, being associated with high temperatures. As it is almost -insoluble in water, like cassiterite and ilmenite, it is likely to occur -with them in the sands which are the result of the disintegration of the -rocks which carried the minerals; and so a large part of the supply -today comes from placer deposits. - -It is found in Connecticut, North Carolina, Missouri, Colorado, and -California. - - - Radium, Uranium and Vanadium - -These three metals are all rare and occur together. Radium, discovered -in 1898, is a heavy metal which has proved very useful because of its -radio-activity, that is, its power of giving off or radiating tiny -particles of matter known as _X-rays_, part of which are charged with -positive electricity, and part of them with negative electricity. The -ability of these rays to pass through other substances has made possible -photographing the denser substances within those less dense, as the -bones within the flesh, or metal within leather or wood, etc. The rays -have proved of great value medicinally, and are also used to make -objects luminous in the dark. These X-rays are also used in the study of -the ultimate structure of matter, as it can be thus obtained in such -small units. - -Uranium is another element which is radio-active and can be used for -many of the same purposes as radium. - -Vanadium, the third of these associated metals, and the commonest of the -group, is not radio-active. It is a silvery-white metal, mostly used as -an alloy with steel to give it great hardness. - - -Carnotite -K₂O·2U₂O₃·V₂O₅·3H₂O -Pl. 27 - -Occurs in earthy masses; color yellow. - -This mineral is included here, not because it is common, but because it -is of such great interest. It is the chief source of supply in the -United States of radium, uranium and vanadium. It is a lemon-yellow -earth or powder, which looks a little like orpiment. It is however found -in a sandstone, instead of where hot waters have deposed minerals. From -a ton of this ore about 10 pounds of uranium oxide, 55 pounds of -vanadium and ¹/₁₀₀₀th of a gram of radium are obtained. Carnotite is -found in south-west Colorado and south-east Utah, and on Carrizo -Mountain on the line between Arizona and New Mexico. - - - Mercury - -Mercury, or quicksilver, is the only metal which is liquid at ordinary -temperatures. It is silvery-white in color, with a striking metallic -luster, and at the low temperature of 662° F., boils and changes to a -colorless vapor. Mercury alloys with certain metals, these alloys being -known as amalgams. In this way it is especially useful for the recovery -of gold and silver, the mercury being added to crushed ore, the gold or -silver uniting with the mercury in a liquid amalgam, which is then drawn -off and heated to a temperature above 662° F., at which temperature the -mercury volatilizes and is recovered, while the gold or silver remains -behind. Mercury also forms a solid amalgam with tin which is used to -coat glass, the high metallic luster making the most effective looking -glass. It is also used in medicines (calomel, corrosive sublimate, -etc.), for scientific instruments (thermometers, barometers, etc.), in -cosmetics, in paints for ship bottoms, etc. - -Though there are some 25 minerals of mercury, only one is common or -important as a source of the metal, cinnabar. The United States is -self-sufficient as far as mercury is concerned, producing just about as -much as it uses. The leading producers are Spain, Austria, Italy, and -the United States. Commercially mercury is quoted as quicksilver, and in -flasks of 75 pounds each. - - -Cinnabar -HgS -Pl. 27 - -Occurs in massive or earthy form, or in minute crystals in cavities; -hardness 2.5; specific gravity 8; color scarlet to dark red; streak -vermilion; luster adamantine; translucent on thin edges. - -The bright-red color and the streak are usually enough to identify this -mineral at once, but some of the darker varieties resemble hematite or -zincite in appearance, but both these have much greater hardness. When -in crystals they are tiny hexagonal prisms with pyramids on the end. -Cinnabar is usually found in or near metamorphic or igneous rocks, -either in veins leading from the igneous rocks, or in metamorphic rocks, -or it may occur disseminated through metamorphic rocks. It is associated -with quartz or calcite, and may occur with other sulphides like pyrite, -galena, argentite, etc. It is most abundant in California, but is also -found in Oregon, Washington, Idaho, Arizona, Nevada, Utah, Texas, and -Montana. - - - Tin - -Tin has been known since early Roman times, and the mines at Cornwall, -England, were worked from that time all through down to the present, but -now they are becoming of minor importance as they approach exhaustion. -The metal is silvery-white, does not easily tarnish, is malleable, but -has little ductility and little tensile strength. Tin is mostly used in -making tin plate, a thin sheet of steel covered with tin, the tin being -only 1 to 2% of the total weight. This tin plate is mostly made into tin -cans, and used as containers for food. Some tin is used in making -solder, tin-foil, tubes for paste, vaseline, etc., and around 1000 tons -per year for weighting silk. This “weighting” makes the silk heavier by -about 25% and gives it a “rustle,” which, while much in evidence, is -really indicative that the silk is not pure. The United States produces -very little tin, most of the world’s supply coming from the Malay -Peninsula, Dutch East Indies, China, and Bolivia, with small amounts -from several other countries. - - -Cassiterite -SnO₂ -Pl. 28 -_tin stone_ - -Occurs in tetragonal crystals, massive, or in grains and pebbles; -hardness 6.5; specific gravity 7; color black or dark-brown; streak -gray; luster adamantine; translucent on thin edges. - -The crystals are short prisms with pyramidal ends. Twinning is common. -Cassiterite also occurs in fibrous masses, and when it is weathered from -its original location, is so insoluble and hard, that it remains as -grains and pebbles, making placer-deposits, from which today three -quarters of the supply is obtained. If pure, the crystals would be -colorless, but impurities of iron and titanium give it the dark-brown to -black color. Cassiterite may appear very like rutile, the crystalline -forms being identical, but the reddish tinge of color in the rutile will -separate the two. - -Cassiterite is one of those minerals which result from deposition at -very high temperatures, probably from vapors, and is found in the veins -in igneous rocks, such as light-colored granites, gneisses, syenites, -etc. While not mined in this country it is found in small quantities in -Maine, Massachusetts, New Hampshire, Virginia, Alabama, Wyoming, -Montana, and California. - - - Titanium - -Titanium, as a metal, is a heavy, gray, iron-like powder, which is -chiefly useful as an alloy with iron, giving it toughness, and -preventing bubbles and cracks in casting. It is not as rare as some -other metals which have found a wider use. - - -Rutile -TiO₂ -Pl. 28 - -Occurs in tetragonal crystals, and in grains; hardness 6.5; specific -gravity 4.2; color red to reddish-brown; streak yellowish-brown; luster -metallic to adamantine; translucent on thin edges. - -Rutile usually occurs in crystals, which are either short and stout, or -in needle-like crystals. Twinning is common. In form and general -appearance it resembles cassiterite, but the reddish color, and the -yellowish-brown streak will distinguish the rutile. It is found in -similar rocks, granites, gneisses, syenites, and mica-schists, the two -minerals cassiterite and rutile often occurring together. This is also -true of the grains, which have been weathered out and are found in sands -and gravels of placer deposits. It is found in small quantities in all -the New England States, New York, and all down the Appalachian -Mountains, especially at Graves Mountain, Ga., and in Arkansas and -Alaska. - - -Ilmenite -FeTiO₃ - -Occurs in granular masses, as black sand, or as tabular hexagonal -crystals; hardness 5-6; specific gravity 4.7; color black; streak -brownish-red to black; luster metallic; opaque on thin edges. - -When ilmenite occurs in crystals they are tabular and resemble hematite -in its darker varieties, but the streak readily distinguishes the two. -In masses it looks like magnetite, but the lack of magnetism serves to -distinguish these two minerals. It is very likely to be associated with -cassiterite, rutile, or magnetite in grains which have weathered out of -the original rock, and have resisted solution and wear. Sands with a -large amount of the above mentioned minerals are termed “black sands,” -some of which are important for one or another of these minerals. - -Ilmenite is a mineral formed at high temperatures, and probably often -deposited from hot vapors. It is found in granites, syenites, and -gneisses. Among the better known localities are Orange, N. Y., -Litchfield, Conn., Florida, California, etc. - - - Platinum - -This metal is steel-gray in color, very malleable and ductile, almost -infusible and resists the action of acids. It is one of the “noble” -metals, much rarer than gold, and so has become popular for jewelry. It -is also used in the manufacture of sulphuric-acid, in nitrogen-fixation -plants, for chemical utensils, in the electrical industries, and in -dentistry. Platinum in its occurrence is associated with the certain -other equally rare elements, like iridium, palladium and osmium. Its use -has increased rapidly of late, but the supply has not kept up with the -demand, so that, whereas in 1906 platinum and gold were about equally -valuable, now the platinum brings about five times as much as the gold. - - -Platinum -Pt - -Occurs in grains or nuggets; hardness 4.5; specific gravity 19 (21 if -pure); color steel-gray; luster metallic; opaque. - -This rare metal is mostly found in placer-deposits, often with gold. It -comes originally from dark igneous rocks, like peridotite, pyroxenite, -etc., and platinum is found to be associated with the nickel ores of -Sudbury, Canada. While formerly 90% of the world’s supply of platinum -came from placer mines in the Ural Mountains, today more than half is -produced in Canada and about a fifth in Russia. In the United States it -is found in California, Oregon, Nevada, and Alaska. - - - The Magnesium Group - -Magnesium is a silvery-white metal, easily tarnished by exposure to -moist air. Because of its light weight, less than twice the weight of -water, and strength, it is being substituted for aluminum, especially in -airplanes, where the question of weight is crucial. It is also used in -automobile and ship production and other machine industries, and in the -manufacture of flares and incendiary bombs. Magnesium is obtained -chiefly from magnesite, dolomite, and in the United States as a result -of a recently developed process, from sea water. Magnesium has a -considerable number of minerals, of which three are taken up here and -several more under the head of silicates, where both magnesium and -silicon are combined in a mineral. - - -Spinel -MgAlO₄ -Pl. 29 - -Occurs mostly as isometric octahedrons; hardness 8; specific gravity -3.5; color, red, yellow, green, or black; streak white; luster vitreous; -transparent on thin edges. - -This is a rather rare mineral, but, when in clear crystals is considered -one of the gems. It was early confused with corundum, and the red -variety called ruby, as it was found in the same gem-bearing sands in -Ceylon, Burma, and Siam. However the form of the isometric octahedron as -compared with the hexagonal prism of the corundum, together with the -lesser hardness are sufficient to distinguish the two easily. The -crystals are usually octahedrons, but may have the corners cut or the -edges beveled. Twins are not uncommon. - -The standard color is a clear deep-red, and such a spinel is known in -the gem trade as a _spinel-ruby_. If the color is rose-red, it is a -_Balas ruby_; if orange, it is _rubicelle_, if of a violet tinge, -_almandine_. When small quantities of other elements replace the -magnesium, the color is greatly changed. For example a little iron -present gives the crystals a dark-green to black color, and the spinel -is known as _ceylonite_. If there is both iron and chromium present, the -color becomes yellowish or greenish-brown, and this variety is -_picotite_. When the impurities are iron and copper, the color becomes -grass-green, and it is called _chlorospinel_. A form, in which the -magnesium is completely replaced by iron, is black in color and termed -_hercynite_, and occurs fairly abundantly in Westchester Co., N. Y. From -Amity, N. Y., to Andover, N. J., there is a belt of granular limestone -in which spinel of all colors is found. St. Lawrence Co., N. Y., is also -a rich locality. Bolton, Mass., Newton, Sterling, and Sparta, N. J., -North Carolina, Alabama, and California all yield spinel. - - -Magnesite -MgCO₃ - -Occurs in cleavable or compact porcelain-like masses; hardness 4; -specific gravity 3.1; color white to gray; luster vitreous; translucent -on thin edges. - -Magnesite is white and brittle, and cleaves perfectly parallel to the -faces of the rhombohedron, but it seldom occurs in crystals. It will -effervesce in warm hydrochloric acid and has some resemblance to -calcite, but can be distinguished by the greater hardness. It is still -more like dolomite, both having the same color and cleavage, both -effervescing in warm hydrochloric acid; but the magnesite has half a -point greater hardness and the porcelainous appearance. Magnesite is -used in toilet preparations, paper making, and mixed with asbestos, as a -covering for heating pipes. - -Magnesite is found in Massachusetts, Pennsylvania, Texas, and in large -deposits in California and Washington. - - -Dolomite -(MgCa)CO₃ -Pl. 19 & 29 - -Occurs in crystals, or in cleavable or granular masses; hardness 3.5; -specific gravity 2.8; color white to pink or gray; streak white; luster -vitreous; transparent on thin edges. - -Dolomite crystallizes in the hexagonal system, in rhombohedrons -(hemihedral form), which are more or less modified by faces on the -corners or edges. The cleavage is parallel to the rhombohedron, and it -will effervesce in warm hydrochloric acid. Sometimes the crystal faces -are curved, and when this is the case, dolomite is easily determined. -Usually however dolomite resembles both calcite and magnesite. From the -calcite it is distinguished by the greater hardness, and from magnesite -by lesser hardness and not being porcelainous in appearance. Some of the -commoner forms are shown on Plate 29, crystals like C being found -embedded in anhydrite and gypsum. - -Magnesium is a common element and is likely to be present wherever lime -is being deposited, so dolomite crystals are common, and much of the -limestone is dolomitic. - -It may be found in almost any limestone section of the country. Some of -the finest crystals of dolomite however come from Roxbury, Vt., -Smithfield, R. I., Hoboken, N. J., Lockport, Rochester, and Niagara -Falls, N. Y., etc. - - - Silicon, Silica and the Silicates - -Silicon is one of the non-metallic elements, and does not occur as such -in Nature. When isolated it is either a dark-brown powder, or steel-gray -crystals. However silicon is next to oxygen in its importance in making -the crust of the earth. Forty-seven per cent of the surface rocks are -composed of oxygen, and 28% of silicon, the latter appearing in a host -of minerals. The oxide of silicon is termed silica (SiO₂), its crystal -form being quartz, the commonest of all minerals. In non-crystalline -form silica is also widely distributed, as chalcedony and opal, even -appearing in the tissues of animals and plants, as in the feathers of -birds, the shells of certain Protozoa (Radiolaria), the spicules of -sponges; and in plants, as the shells of diatoms, and in the stalks of -grasses, especially cereals and bamboo. Silica in the form of sand is -widely used in making glass, porcelain, china, etc., and in the various -cements. - -Then there are a considerable number of acids of silicon, which do not -occur in Nature, but their salts do, and make a host of minerals, which -are known as the silicates, such as mica, feldspar, hornblende, etc. -Either as quartz, or as silicates, silicon is represented in most all -the igneous and metamorphic rocks and in many of the sedimentary rocks. - - -Quartz -SiO₂ -Pl. 30 - -Occurs as hexagonal crystals, or in grains or masses; hardness 7; -specific gravity 2.65; colorless when pure; luster vitreous; transparent -on thin edges. - -Quartz is not hard to identify. Its hardness and the crystal-form -separate it from most all other minerals. It is the most common mineral, -making 12% of the earth’s crust. The usual crystal form is a hexagonal -prism with the sides horizontally striated, and a six-sided pyramid on -one or both ends. This six-sided pyramid is really two rhombohedrons, a -right-handed one and a left-handed one, so that the alternate faces of -the pyramid may show peculiarities, for instance three may be large and -three small, as in Fig. B, Plate 30, or the alternate ones may be duller -or etched in some manner. The crystals are clear and when pure -colorless, but there is a tendency for some slight impurity to color -them almost any hue. - -The most perfect double-ended crystals form only where growth is -possible in all directions, as in clay. In cavities and caves there is -an opportunity for the crystals to grow in toward the open spaces, and -in such places, one finds fine large crystals; the Alps, Brazil, Japan, -and Madagascar being especially famous localities. The largest quartz -crystal on record is one 25 feet in circumference which came from -Madagascar. In this country the caves at Little Rock, Ark., have -furnished some very fine large crystals. Smaller, but very clear -crystals, come from about Herkimer, N. Y. Some of these have been used -as “Rhine-stones” and as cheap imitations of diamonds. Clear quartz is -beautiful enough to be a gem, but it is too common to interest people as -jewelry, however many objects of art have been carved from it. One of -these took the form of crystal balls, which, through the Middle Ages -particularly, developed into a form of mysticism. The gazing into the -crystal ball was supposed to give some people supernatural vision. It -seems to be a form of hypnotism, gazing at the bright reflecting surface -tiring the eye, and making possible visions, which are subjective rather -than anything external. - -Silica is slightly soluble in water, especially when it is alkaline; so -that most river-, lake-, and sea-waters have some silica in solution, -and are carrying it from one place to another. The waters, which -percolate through the rocks, carry even more, and when they come out -into open spaces, they give up some of the silica, making crystals -lining these openings, whether fissures or cavities. Not infrequently -these silica-bearing waters dissolve out some other crystal, and then -deposit in its place silica, thus making a crystal which has the form of -what was dissolved, rather than that of quartz. Such a form is known as -a pseudomorph. - -When molten masses of igneous rock were cooling the quartz crystals had -their faces interfered with as they grew, and we have resulting -crystalline quartz, simply filling in the spaces between the other -crystals, such as feldspar and mica, in the granite. Quartz is a large -component in many igneous rocks, also in metamorphic rocks, and certain -sedimentary rocks like sandstone are almost wholly made up of quartz -grains. Quartz is also the gangue mineral in many veins. In this case it -seems to have been deposited from hot water or vapors, as they rose from -cooling magmas. With it are associated all sorts of metallic ores as has -been suggested. - -Quartz has been largely used to make imitations of other much rarer -minerals, sometimes in its crystalline form to imitate the diamond, at -other times ground and made into a “paste,” which is colored to imitate -other gems. This paste is a mixture of about 4 parts of quartz, 5 parts -of red lead and 1 part of potassium carbonate, melted and cooled slowly. -It is clear and has a brilliant luster like the diamond. If some -coloring matter is put into it it can be used for rubies, sapphires, -etc. When there is any reason to think that this is being used, it is -easily detected by being so much softer than any of the true gems, and -even than true quartz. Quartz will scratch glass readily, but this -imitation has only the hardness of very soft glass, or about 5. - - - Varieties of Quartz - -Rock crystal is the term applied to quartz when it is clear and -colorless. - -Milky quartz is the milky variety, the whiteness being due to -imperfections in the crystallization, such as cracks, bubbles, etc. - -Smoky quartz is the cloudy brown-colored variety, which results from the -presence of small quantities of organic matter (hydrocarbons) in the -quartz. If the color is so dark as to be almost black it is termed -morion. In the above cases the color will disappear if the stone is -heated. Pebbles of smoky quartz from Cairngorm, Scotland, have been so -widely used as semiprecious stones that they have come to be known as -cairngorms. - -Citrine, or false topaz, is a clear yellow variety, the color again due -to the presence of organic matter. It is distinguished from true topaz -by the lesser hardness, this having the hardness of 7, while true topaz -has a hardness of 8. - -Amethyst is quartz with a violet color, due to the presence of small -quantities of manganese. To be suitable for cutting into gems, the color -must be deep or the small pieces will appear almost colorless. It is -widely used today as a semiprecious stone in jewelry; and in the -fifteenth century it had the traditional virtue of making the wearer -sober-minded, whether he had taken too freely of wine, or was over -excited by love-passion. - -Rose quartz gets its pale-red color from the presence of a small amount -of titanium. It is widely distributed, but is more abundant in the Black -Hills of South Dakota. - -Aventurine is quartz which has inclosed tiny scales of mica or hematite -giving it a spangled appearance. - -Prase is a green quartz, the color being due to the inclusion of fibrous -crystals of green actinolite. - -Cat’s Eye is a quartz which has inclosed silky fibers of asbestos. When -this is cut parallel to the fibers, the effect is opalescent. The colors -are greenish, yellowish-gray, and brown. This form, however, is not to -be confused with the true or Oriental Cat’s Eye, which is chrysoberyl -and has the hardness of 8. - - -Chalcedony -SiO₂ - -Non-crystalline, occurring in botryoidal, stalactitic or concretionary -masses; hardness, 7; specific gravity, 2.65; color white when pure; -luster waxy; translucent to transparent on thin edges. - -In addition to the crystalline form, silica is freely deposited in an -amorphous or cryptocrystalline form which has the same properties as -quartz, except the crystal faces. This is called chalcedony, and it -occurs in seams, cavities and free surfaces. When the surface of a -chalcedony deposit is free it has a waxy luster. It is generally very -brittle and breaks in a peculiar splintery manner. Like quartz it also -has a great many varieties, according to the impurities present. Its -wide distribution, hardness, and the manner in which it can be chipped -have made this a most important stone in the history of the development -of civilization. The early men first broke it into rough tools, such as -knives, axes, spear points, etc., and used these as cutting tools, of -one sort or another, because they held their edge better than most -stones. We apply, to the people who used only these chipped stones as -tools, the term “_Men of the Old Stone Age_,” or the period is termed -the _Palæolithic Age_. Later men learned how to grind the edge to a -smoother outline, and this much shorter period is termed the _Neolithic -Age_. The use of flints for the first tools is world-wide, and the -American Indian when discovered was still using chalcedony in its -rough-hewn state. - - “There the ancient Arrow-maker - Made his arrow heads of sandstone, - Arrow heads of chalcedony, - Arrow heads of flint and jasper, - Smoothed and sharpened at the edges, - Hard and polished, keen and costly.” - -Chalcedony is the proper term to use when the color is white to -translucent, in which case the surfaces are usually botryoidal and waxy. - -Carnelian is chalcedony which is clear red in color and translucent. -This is one of the first stones used for ornamental purposes and for -engraving. Carnelians with figures engraved on them were used by the -Egyptians, Assyrians and The Children of Israel, at least 2000 B.C.; and -the Egyptian scarabs of the fifth or sixth century B.C., were often -carved from this variety of chalcedony, as well as from jasper and -agates. - -The brownish varieties are termed _sard_. - -Chrysoprase is an apple-green variety of chalcedony the color being due -to the presence of nickel oxide. This is by no means as common as most -of the varieties of chalcedony, and was long prized as a gem. - -Plasma is chalcedony with a leek- to emerald-green color, and the same -stone when it has small red spots of jasper in it is termed -_blood-stone_, or _heliotrope_. These red spots are said by tradition to -be drops of the blood of Christ. - -Jasper is a deep red chalcedony, the color being due to hematite, which -is so abundant as to make it opaque. A brown variety colored by limonite -is also called jasper, and even green jaspers are found. In all cases -the opaque character is common. - -Flint is an impure brown chalcedony, usually forming concretions. The -color is due to organic matter. Flint is mostly found in limestone or -chalk, and the concretions are the result of the small particles of -silica scattered through the rock being dissolved, and then -reprecipitated about some organic center. Generally the silica was -obtained by the dissolution of small fossils, like the shells of diatoms -or sponge spicules. - -Hornstone and Chert are simply impure varieties of flint, brown in -color, and with a splintery fracture. - -Agate, Plate 32, is a banded or cloudy chalcedony which has formed in a -cavity, the layers of different color representing deposition from -water, carrying first silica with one impurity, then later, silica with -another impurity. Gradually the cavity has been thus filled with silica; -and when the mass is freed by the weathering away of the surrounding -rock, these banded masses are found. Sometimes the manner of deposition -has changed, and while the outer part of the cavity was filled with -chalcedony, the central part will contain quartz crystals. On account of -the beauty of the colors, and the unusual way in which they may be -developed, agates are widely used for semiprecious jewelry and objects -of art, and this has been true since ancient times, the name itself -coming from the River Achates in Sicily. The center for cutting and -polishing agates is at Oberstein, Germany, where this work has been -carried on since the middle of the fifteenth century. In spite of the -many fine natural colors in agates, they are sometimes artificially -colored, in many cases by methods which are kept as “trade secrets.” The -color seldom penetrates far; so that even slight chipping reveals -whether an inferior agate has been taken and colored up, or whether the -stone is natural. Moss agates are chalcedony which has inclosed -dendritic masses of some one of the manganese compounds as shown under -manganite, p. 73. - -Onyx is a variety of agate where the bands are alternately black and -white; while sardonyx is agate with red or brown bands alternating with -the white. Such agates as these are especially desirable for cameo work, -where the figure is carved in the chalcedony of one color, and the other -color makes the background. - -Silicified or _agatized wood_ is a form of chalcedony, where silica has -replaced wood, molecule by molecule; so that in good specimens, all the -structure of the wood is still retained, and when thin sections are made -it can be studied under the microscope almost as well as modern wood. -This takes place under water, usually, if not always, in fresh water. -Such fossilized wood is widely distributed in the western United States, -the most famous cases being the Fossil Forest of Arizona, now a National -Reservation, and the fossil trees in the Yellowstone National Park. - - -Opal -SiO₂·H₂O -Pl. 33 - -Non-crystalline, massive, stalactitic or nodular; hardness, 6; specific -gravity 2; all colors; luster vitreous, resinous, or pearly; transparent -on thin edges. - -Opal differs from chalcedony in having water, usually about 10%, -incorporated in its structure. This is water of crystallization, and not -firmly held; so that, if opal is heated in a closed tube to above 100 -C., it is given off as a vapor. Opal is distinguished from chalcedony by -its lesser hardness, and the resinous to pearly luster. It forms in -cavities, in layers often of extreme thinness. - -Opal is originally the product of the dissolution of silicate minerals -in hot acid waters, the resulting gelatinous silica, when it is -deposited and hardened, becoming the opal. There are many varieties, -some of them highly prized as gems in spite of the moderate hardness and -opacity of the mineral. Gem-quality opal gets its opalescent character -from the successive deposition of thin films of opal, the light -penetrating and being reflected from different films. This breaks up the -white light and causes the play of colors which is the charm of this -gem. - -Precious opal, in which the play of colors is finest, comes mostly from -Hungary, Mexico, and Queensland. The opal was a favorite stone from -before Roman times, and in its early history was a charm against the -“evil eye.” During the nineteenth century for some reason it came to be -considered an unlucky stone. - -Fire opal is a hyacinth-red to honey-yellow variety, which has a -fire-like play of color, and is found in Mexico and Honduras. - -Common opal does not have the play of color, but comes in a variety of -colors; is waxy or greasy in luster; and occurs mostly as fillings of -seams or cavities, especially those in igneous rocks, like the steam -holes in lavas, etc. It is found in Cornwall, Penn., in Colorado, -California, etc. - -Opal-agate is a variety in which there are color bands, and it is widely -distributed. - -Opalized wood is formed in exactly the same manner as agatized wood, -much of the fossil wood called silicified being really opalized. - -Siliceous sinter is the porous mass of opal which is so frequently -deposited about hot springs and geysers. It is readily recognized by its -porous character. - -The shells of the diatoms, which are microscopic plants, are made of -opal; and while they are so small, there is certainly no other plant so -abundant or omnipresent, living as it does in every pool, lake, or sea -by the millions. These shells are very indestructible so that they -accumulate at the bottom of ponds, bogs, and sea-bottoms, making at -times extensive deposits. This material in quantities is termed -diatomaceous earth, or tripolite (from Tripoli where it was first used -commercially). It is used as a polishing powder for metals, marble, -glasses, etc. - - - The Feldspars - -The term feldspar is a family name for a large variety of very common -minerals, which altogether make up nearly 60% of the crust of the earth, -being the predominant part of granites, gneisses, and lavas. In -composition they are silicates of aluminum, together with potassium, -sodium and calcium, and their mixtures. They may be tabulated as -follows: - - 1. KAlSi₃O₈, _orthoclase_, the silicate of aluminum and potassium. - 2. NaAlSi₃O₈, _albite_, the silicate of aluminum and sodium. - 3. CaAlSi₂O₈, _anorthite_, the silicate of aluminum and calcium. - 4. Mixtures of 1 and 2 are _alkalic feldspar_. - 5. Mixtures of 2 and 3 are _plagioclase feldspar_. - -Orthoclase is monoclinic, but the rest of the feldspars are triclinic. -If crystals are available they may be short and stout, or tabular and -thin, but as the feldspars are mostly components of the igneous rocks, -where perfect crystals have not had a chance to grow, they are mostly -determined by their hardness and cleavage. The hardness of all the -feldspars is 6 or very close to it. - -They all have three planes of cleavage, two of which are good and -intersect either at 90° as in orthoclase, or at about 86° as in the -plagioclase series; while the third cleavage plane is imperfect. In -figure 1, Plate 34, a and b are the two perfect cleavages, while c is -the imperfect one. Breaking into such cleavage masses as the one -illustrated is characteristic of feldspar. The specific gravity ranges -from 2.55 to 2.75. The luster is vitreous, and the color white, ranging -to various shades of gray and pink, and, sometimes in recent lavas, -colorless. - -Twinning is very common and helps to distinguish orthoclase from the -plagioclase feldspars. In orthoclase the twins are simple, that is, only -two crystals growing together, and are united on one of the faces, as if -one of them had been revolved 180° with the other; or, while related to -each other as in the preceding case, they may seem to grow through each -other. On plate 34 are three orthoclase crystals showing this simple -type of twinning. The first (A) is a simple crystal; the second (B) -shows the simplest type of twinning where the left-hand crystal has -revolved 180° on the p face, and the end is composed, half of the upper -end of one crystal, and half of the lower end of the adjacent crystal. -The presence of reëntrant angles calls attention to the twinning. The -third figure (C) is a case of intergrowing crystals. - -In the plagioclase feldspars twinning is multiple, a large number of -crystals, each thin, sometimes as thin as paper, growing side by side, -the first one in normal position, the next at 180° with it, the third -revolved 180° to the second and thus parallel to the first, and so on. -The result is first of all a striated appearance, and second that, as -plagioclase crystals have their prism faces intersecting at 86°, there -is a series of low roofs and valleys, which are best seen by holding the -piece of feldspar so the light reflects from a cleavage face, when it -will appear striated; then by tilting it about 8 degrees a second set of -reflections, also appearing striated, will appear. The light was first -reflected from one side of the roofs, and in the second case from the -other side. Figure D, Pl. 34, is a diagram showing the relation of the -individual crystals in a multiple twinned piece of plagioclase, in which -the crystals are represented as rather large. Plate 35, under -labradorite, shows a photograph of a cleavage piece, on which is readily -seen the striation which is characteristic of the plagioclase feldspars. - -Mixtures of albite and anorthite occur in bewildering numbers, one or -the other predominating, and each mixture being uniform throughout the -crystal and in the whole mass; so each combination is a mineral, each -with its special properties; but the different plagioclase feldspars are -so similar in appearance, that by the naked eye it is impossible to -separate the closely related ones. This can be done under the microscope -by studying the angles at which light is cut off, and also by chemical -analyses. For our purposes six types will suffice to illustrate the -group, and their composition may be indicated as follows. - -Albite is albite with up to 15% of anorthite mixed with it. - -Oligoclase is albite with from 15-25% of anorthite mixed with it. - -Andesite is albite with from 25-50% of anorthite mixed with it. - -Labradorite is anorthite with from 25-50% of albite mixed with it. - -Bytownite is anorthite with from 15-25% of albite mixed with it. - -Anorthite is anorthite with up to 15% of albite mixed with it. - -The best method for distinguishing these feldspars of the plagioclase -group is to measure the angle between the two perfect cleavage faces, -and even this requires careful measurement. The angles between these -faces are as follows: - - Orthoclase 90° - Microcline 89° 30′ - Oligoclase 86° 32′ - Andesite 86° 14′ - Labradorite 86° 14′ - Bytownite 86° 14′ - Anorthite 86° 50′ - - -Orthoclase -KAlSi₃O₈ - -Occurs in granites, syenites, gneisses and light-colored lavas; -hardness, 6; specific gravity, 2.57; color white to gray or pink; -cleavage in two directions perfect and at 90°, in the third direction -imperfect; luster vitreous; translucent on thin edges. - -Orthoclase is monoclinic, and when formed in cavities develops as -crystals, but it is usually a constituent of igneous rocks, in which -case the crystals have not had the opportunity to develop the crystal -faces, and the orthoclase is in grains or irregular masses; and the best -way of determining the mineral is the cleavage, the two perfect cleavage -planes intersecting at right angles. Twinning is frequent but of the -simple type, only two crystals being united, similar to either B or C on -plate 34. - -It is found in granites, gneisses or lavas, wherever they occur, being -especially characteristic of the granites of the Rocky Mountains. - - -Microcline -KAlSi₃O₈ -Pl. 35 - -Occurs in granites and gneisses as crystals or irregular masses; -hardness, 6; specific gravity, 2.56; color white to gray, pink, or -greenish; luster vitreous; translucent on thin edges. - -Microcline has the same composition as orthoclase, but is in the -triclinic system, the c axis being inclined a half degree away from a -right angle with the b axis. This is best seen in the cleavage pieces, -the two perfect cleavage planes meeting at 89° 30′, and this is the only -test for determining this mineral by the unaided eye. Pike’s Peak is the -best known locality for microcline, and there it occurs in fine large -crystals of greenish color, which are known as _Amazon stone_. - - -Albite -NaAlSi₃O₈ - -Occurs in small crystals, or more often in lamellar masses in granites -or in seams in metamorphic rocks; hardness, 6; specific gravity, 2.62; -color white to gray; luster vitreous. - -Albite may occur in simple crystals, in which case the two perfect -cleavage planes meet at an angle of 86° 24′. However, it is much more -frequently found twinned in the multiple manner, the individual crystals -often being as thin as paper. This gives rise to a fine striation on the -end of a crystal, or on the surface made by the imperfect cleavage -plane. Where the crystals are extremely thin, the surface may have a -pearly luster. Albite types of granite often inclose secondary minerals, -that are prized as gems, such as topaz, tourmaline, and beryl. - -It is found at Paris, Me., Chesterfield, Mass., Acworth, N. H., Essex -Co., N. Y., Unionville, Penn., and in Virginia, and throughout the Rocky -Mountains. - - -Oligoclase -(NaCa)AlSi₃O₈ - -Generally found in cleavable masses in granites and lavas, rarely in -crystals; hardness, 6; specific gravity, 2.65; color white, greenish or -pink; luster vitreous; translucent on thin edges. - -Oligoclase is a plagioclase feldspar and is distinguished by its two -perfect cleavage planes meeting at an angle of 86° 32′, but otherwise it -is very like albite. Crystals are not common, and it occurs mostly in -masses, making one of the components of granite or lava. - -It is found in St. Lawrence Co., N. Y., Danbury and Haddam, Conn., -Chester, Mass., Unionville, Penn., Bakersville, N. C., etc. - - -Labradorite -(NaCa)AlSi₃O₈ -Pl. 35 - -Usually found in cleavable masses in granites and lavas; hardness, 6; -specific gravity, 2.71; color gray or white, often with a play of -colors; luster vitreous; translucent on thin edges. - -Labradorite is distinguished by having the two perfect cleavage planes -meet at 86° 14′. The iridescent play of color is also very -characteristic and is generally present. It is due to the inclusion of -minute impurities. This feldspar is usually associated with granites or -lavas in which the dark minerals predominate. It gets its name from -being the feldspar of the granites of Labrador, and is also found in the -granites of the central part of the Adirondack Mountains and the Wichita -Mountains of Arkansas. - - - The Pyroxene Group - -The minerals of this group are generally associated with feldspars, and -make the dark-colored component of granites, gneisses and lavas. This is -especially true of those which have some iron in the crystal. Pyroxenes -are salts of metasilicic acid (H₂SiO₃), in which the hydrogen (H) has -been replaced by calcium, magnesium, iron, etc. The commoner minerals -are orthorhombic or monoclinic, and all agree in their crystal habit, -being short stout prisms, with the vertical edges so beveled that a -cross section is eight-sided. The cleavage is good in two directions, -parallel to the beveling faces (m in figure b, Plate 36), and they -intersect at an angle of 87°. This is very characteristic, and if one -has a crystal broken across, it is easy to see and measure this angle of -intersection. These pyroxenes have the same chemical composition as the -corresponding series of amphiboles, but the two are distinguished by -several features. Pyroxenes are short and stout crystals, while -amphiboles are long and either blade- or needle-like; pyroxenes are -eight-sided in cross section, while amphiboles are six-sided; in -pyroxenes the cleavage planes intersect at 87°, while in amphiboles they -intersect at 55°. The minerals of this group are most frequently one of -the components of a lava or granite, and are less frequently associated -with metamorphic rocks. Three are common; enstatite, hypersthene, and -augite. - - -Enstatite -MgSiO₃ - -Usually occurs in lamellar or fibrous-lamellar masses in dark lavas; -hardness, 5.5; specific gravity, 3.3; color gray, bronze or brown; -luster vitreous, translucent on thin edges. - -Enstatite rarely occurs in crystals, but when it does they are -orthorhombic. Usually it is in irregular masses with the cleavage -angles, typical of pyroxene. The color is light, that is gray or -brownish, and the streak white or nearly so. In most respects it is -similar to hypersthene, which has the same composition, except that a -large part of the magnesium is replaced by iron, and there are all sorts -of gradations between the two minerals. When some iron takes the place -of magnesium, the color darkens to, or towards bronze, until when about -a third of the magnesium is so replaced, and the color is fully bronze, -this variety is called _bronzite_. Bronzite is present in some of the -dark lavas like gabbro and peridotite. Enstatite is found in the -Adirondack Mountains, at Brewster and Edwards, N. Y., etc. - - -Hypersthene -(MgFe)SiO₃ - -Occurs in cleavable masses in dark lavas; hardness, 5.5; specific -gravity, 3.4; color dark-brown or greenish-brown; luster vitreous; -translucent on thin edges. - -Hypersthene is a pyroxene in which magnesium and iron are present in -about equal quantities. It is similar to enstatite, except that the -color is darker, and the streak gray or brownish-gray in color. These -two minerals grade into each other, so that there are cases where it is -simply a matter of preference as to which name should be given to the -mineral. This form is associated with dark lavas, of the gabbro or -peridotite type, in such places as the Adirondack Mountains, Mount -Shasta in California, Buffalo Peaks, Colo., etc. - - -Augite -CaMg(SiO₃)₂, MgAlSiO₆ + Fe₂O₃ -Pl. 36 - -Usually occurs in short stout monoclinic crystals; hardness, 5.5; -specific gravity, 3.3; color dark-green to black; luster vitreous; -translucent on thin edges. - -Augite is a complex pyroxene having some iron and aluminum always -present in it, but the amount not a fixed quantity. It is by far the -commonest of the pyroxenes and has a wide distribution, both in the -sorts of lavas in which it appears, and in the world. It is commonly the -dark component of such lavas, as gabbros and peridotites, and also is -common in metamorphic rocks, especially impure crystalline limestones. -It is found at Raymond and Mumford, Me., Thetford, Vt., Canaan, Conn., -in Westchester, Orange, Lewis and St. Lawrence Counties of N. Y., in -Chester Co., Penn., at Ducktown, Tenn., Templeton, Canada, etc. - - - The Amphibole Group - -The amphiboles are a group of minerals made up of the same chemical -elements as the pyroxenes, but with the molecular arrangement different, -which appears in the forms of the crystals. The commoner ones are all -monoclinic but contrast with the pyroxenes as follows. Amphiboles are -long and slender crystals, while pyroxenes are short and stout; -amphiboles are six-sided, while pyroxenes are eight-sided; amphiboles -have the two perfect cleavages intersecting at 55° and 125°, while those -of pyroxene intersect at 87° and 93°. With the above in mind it is easy -to place the minerals in their proper group, but inside the group it is -not always so easy to distinguish one from another. This group is -associated rather with metamorphic rocks than with igneous rocks, with -which the pyroxenes are mostly associated. The three commoner minerals -of the group are tremolite, actinolite, and hornblende. - - -Tremolite -(CaMg)₃(SiO₃)₄ -Pl. 37 - -Occurs in long prismatic crystals or in columnar or fibrous masses; -hardness 5.5; specific gravity, 3; color white to gray; luster vitreous; -transparent on thin edges. - -The long prismatic crystals of tremolite occur especially where -dolomitic limestones have been altered by metamorphism. Sometimes these -crystals grow side by side, making fibrous masses, where the long -slender crystals can be picked apart with the fingers, and yet are -flexible, and tough enough so that they can be felted together. This is -termed asbestos, which, because it is infusible and a poor conductor of -heat, is much used to make insulators, fire-proof shingles, and all -sorts of fireproof materials. The varieties in which the crystals are -finer and silky in appearance, like the one illustrated on Plate 38 are -termed _amianthus_. There are other minerals, such as actinolite and -serpentine, which occur in the same manner, and are also called -asbestos, the serpentine variety being just now the most important -commercially. - -Tremolite is found at Lee, Mass., Canaan, Conn., Byram, N. J., in -Georgia, etc. - - -Actinolite -(CaMgFe)₃(SiO₃)₄ - -Occurs in radiating crystals, or in fibrous masses; hardness, 5.5; -specific gravity 3; color pale- to dark-green; luster vitreous; -translucent on thin edges. - -Except for its green color, this mineral is very like tremolite. The -difference between the two is due to the small amount of iron in the -actinolite. It is usually found in schists, and the radiating character -of the crystal groups is enough to determine the mineral, if it is -already clear that it is one of the amphiboles. Occasionally it occurs -with the crystals parallel to each other, making one of the forms of -asbestos. - -Actinolite is found at Warwick, Edenville, and Amity in Orange Co., N. -Y., at Franklin and Newton, N. J., Mineral Hill and Unionville, Penn., -Bare Hills, Md., Willis Mt., Va., etc. - - -Hornblende -(CaMgFe)₃(SiO₃)₄CaMgAl₂(SiO₄)₃ -Pl. 37 - -Occurs in well-defined crystals, in grains and in masses; hardness, 5.5; -specific gravity 3.2; color black, dark-green, or dark-brown; luster -vitreous; translucent on thin edges. - -In composition hornblende corresponds to augite, but occurs in long -slender, six-sided crystals with cleavage planes intersecting at 55°, so -that it is a typical amphibole. It occurs in a very wide range of rocks, -such as granite, syenite, diabase, and gabbro; and in such metamorphic -rocks as schists and gneisses; and sometimes igneous rocks are made up -almost entirely of hornblende, when they are known as amphibolites or -hornblendite. It is found all through the New England States, down along -the Piedmont Plateau, through the Blue Ridge Mountains, and in many of -the western mountainous areas. - - - The Garnet Group - -The garnets are a series of double silicates, which occur with -surprisingly uniform characters. They are all isometric, and occur -either as dodecahedrons, or as the 24-sided figure (the trapezohedron), -which is formed by the beveling of the edges of the dodecahedron, and -developing these new faces to the exclusion of the dodecahedron faces. -Combinations of the dodecahedron and trapezohedron (36 faces) may occur. -All the garnets have a hardness of 7 to 7.5, and the specific gravity -runs from 3.2 to 4.3, according to the composition. In size they run -from as small as a grain of sand up to as large as a boy’s marble, and -occasionally even to four inches in diameter. The color varies with the -composition, from colorless to yellow, red, violet, or green. There is -no cleavage, and the luster is always vitreous. - -Garnets are usually accessory minerals, found in metamorphic rocks, -though they are sometimes also present in granites and lavas. They are -always segregations which have taken place in the presence of high -temperatures. When clear and perfect several of the garnets are used as -gems. On the other hand some of the common garnets occur in such -quantities that they are crushed and used as abrasives, for such work as -dental polishes, or for leather and wood polishing. - -The following is the composition of some of the commoner garnets. - - Ca₃Al₂(SiO₄)₃ = grossularite - Mg₃Al₂(SiO₄)₃ = pyrope - Fe₃Al₂(SiO₄)₃ = almandite - Mn₃Al₂(SiO₄)₃ = spessartite - Ca₃Fe₂(SiO₄)₃ = andradite - Ca₃Cr₂(SiO₄)₃ = uvarovite - -Grossularite is chiefly found in crystalline limestones, which have -resulted either from contact with lavas, or from general metamorphism of -impure limestones. These garnets are colorless to white, or more often -shades of yellow, orange, pink, green or brown, according to traces of -impurity which they may contain. The cinnamon-colored variety from -Ceylon is termed _cinnamon stone_, and is a fairly popular gem. - -Pyrope is a deep-red color and when perfect is highly prized as a gem. -It is found in dark-colored igneous rocks, like lavas, or serpentines. -Some of the finest come from South Africa, where they are found in -company with the diamond. - -Almandite is dark-red to brown in color, the brownish-cast -distinguishing it from pyrope. It is one of the garnets known as “common -garnet.” In some cases it is clear and deep colored enough to be used as -a gem, but mostly it is muddy in appearance. The name almandite comes -from Alabanda, a city of the ancient district of Caria, Asia Minor, -whence garnets were traded to ancient Rome. The finest garnets “Sirian -garnets” came from the city of “Sirian” in Lower Burma, and were -supposed to have been found near there, but careful investigation shows -that no garnets occurred near there, and this town was therefore, even -at that early time, a distributing point for garnets, found probably -further to the east. The “Sirian” garnet had a violet cast and now the -term is used to indicate a type of garnet, rather than a locality. - -Spessartite is dark-hyacinth-red, or red with a violet-tinge, and is one -of the less-common garnets. It is usually found in granites. The finest -garnets of the type come from Amelia Court House, Va., which has yielded -some ranging from one up to a hundred carats. - -Andradite is another garnet which is termed “common garnet.” It is red -in color, but with a yellowish-cast which distinguishes it from -almandite, but these two are not easy to separate. It is found mostly in -metamorphosed limestones. One variety is black in color and called -_malanite_. It is found in lavas. The common yellowish-red garnets are -found through New England and the Piedmont Plateau. - -Uvarovite is a rare garnet of emerald-green color, found in association -with chromium ores. - -The number of localities for garnets is so great that a list would -suggest most of the regions where metamorphic rocks occur, as all over -New England, throughout the Piedmont Plateau, the Rocky Mountains, etc. -Certain fine clear garnets, found in Montana, northeastern Arizona, and -northwestern New Mexico are sold under the trade name of “Montana, -Arizona or New Mexico rubies.” These are of fine quality and are mostly -collected by the Indians from the ant hills and scorpion’s nests of -those regions. - -Garnets are among the earliest stones mentioned in ancient languages, as -would be expected from the way these hard and beautiful crystals weather -out of the much softer metamorphic rocks, like schists. In the past -they, with most any other translucent red stone, were included under the -name _carbuncle_. This, however, is not the name of any mineral, but -refers rather to a mode of cutting, _en cabochon_ or with a convex -surface. - - - Glucinum - -Glucinum is a rare metal, silvery-white in color, malleable, and melting -at a fairly low temperature. It is found in the mineral beryl, from -which has come the alternative name _beryllium_. The name comes from the -sweet taste of its salts. Except for beryl its minerals are rare, and -the metal has found but few uses for man. - - -Beryl -Gl₃Al₂(SiO₃)₆ -Pl. 39 - -Occurs in hexagonal crystals in granites, gneisses and mica schists; -hardness, 7.5; specific gravity, 2.7; color usually some tint of green; -luster vitreous; transparent on thin edges. - -When this mineral occurs in coarse hexagonal prisms, with or without -faces on the ends, it is known as beryl; when the crystals are clear and -perfect and of a dark-green color, they are of gem value and are termed -_emerald_; when of a light-green color, they are _aquamarine_; and when -bright-yellow in color, they are the _golden beryl_. There is little -difficulty in determining beryl, for only apatite occurs in such -crystals, and is green, and this latter mineral has a hardness of only -5. There is an imperfect basal cleavage. - -Ordinary beryl is fairly common in granites of the pegmatite sort, and -less common in gneisses and mica-schists. This type often furnishes -crystals of large size, up to two and three feet in diameter. - -Beryl which is free from cracks and inclosures, so it can be used as a -gem, is so rare, that the emerald has a value above that of the diamond, -and second only to the ruby. It is one of the gems with a long history, -having been quarried on the west coast of the Red Sea at least 1650 B.C. -by the Egyptians. To early people it had a power to quicken the prophet -instinct and made the wearer see more clearly. The Spanish -conquistadores found fine emeralds among the treasures of both Mexico -and Peru. In the United States, Stony Point, N. C., was a notable -locality for these gems, but now seems to have been exhausted. The name -emerald has been applied to many other green stones, usually with some -geographical modification, as “Oriental emerald” which is green -corundum, “Brazilian emerald” which is tourmaline, etc. - -Giant beryls have been found at Acworth and Grafton, N. H., and at -Royalston, Mass. Localities for ordinary beryl are Albany, Norway, -Bethel, Hebron, Paris, and Topsham, Me., Barre, Goshen and Chesterfield, -Mass., New Milford and Branchville, Conn., Chester and Mineral Hill, -Penn., Stony Point, N. C., and many other localities in the -Appalachians; also Mount Antero, Colo., and in the Black Hills of South -Dakota. - - -Sodalite -Na₄Al₃Cl(SiO₄)₃ - -Occurs in irregular masses, sometimes in dodecahedrons; hardness, 5.5-6; -specific gravity, 2.3; color deep-blue to colorless; streak white; -luster vitreous; translucent on thin edges. - -This striking mineral, with its deep-blue to azure color, is not easily -confused with any other. It is characteristic of soda-rich igneous rocks -such as syenite and some lavas. In this country it is found at -Litchfield, Me., and Salem, Mass. - - -Zircon -ZrSiO₄ -Pl. 39 - -Usually occurs in tetrahedral crystals in igneous rocks; hardness, 7.5; -specific gravity, 4.7; color brown; luster vitreous; translucent on thin -edges. - -Zircon, the mineral of the rare earth element zirconium, nearly always -occurs in light-colored igneous rocks, like syenite. It may occur in -schists or gneisses, but in these rocks the crystals are of microscopic -size. Because of their great hardness and insolubility, zircon crystals -resist weathering and are often found, along with gold, cassiterite, or -magnetite, in sands which have resulted from the disintegration of -syenite rocks. - -Zircon refracts and disperses light to a degree second only to the -diamond, so that clear crystals are sought as gems. They are often -called “Matura diamonds” because of their abundance at Matura, Ceylon. -When the crystals are colorless or smoky they are termed _jargons_ or -_jargoons_; when of a red-orange hue, they are _hyacinth_ or _jacinth_. -Most of the zircon of gem-quality comes from Ceylon, where it is picked -up as rolled-pebbles from the beds of brooks. - -The most remarkable American locality for zircon is near Green River, in -Henderson Co., N. C., where it is found abundantly in a decomposed -pegmatite dike, from which many tons have been obtained. It is also -found at Moriah, Warwick, Amity and Diana, N. Y., at Franklin Furnace, -and Trenton, N. J., in the gold-bearing sands of California, etc. - - -Cyanite -Al₂SiO₅ -Pl. 40 - -Occurs in long blade-like crystals in gneisses and schists; hardness, 7 -at right angles to the length, and 4.5 parallel to the length; specific -gravity, 3.6; color blue; luster vitreous; translucent on thin edges. - -There are only a few blue minerals, and the way in which cyanite occurs -in long thin blade-like crystals is entirely characteristic. If more is -still wanted to determine this mineral, its unique character in having -the great hardness 7 when scratched parallel to the length, and only 4.5 -when scratched crossways, will settle any doubts. - -The mineral _sillimanite_ has the same composition as cyanite, but is -fibrous in habit and has the hardness 6.5. If cyanite is heated to 1350° -C. it changes its character and becomes sillimanite. - -Cyanite is found as an accessory mineral in metamorphic rocks, such as -gneiss and schist, at Chesterfield, Mass., Litchfield and Oxford, Conn., -in Chester Co., Penn., in North Carolina, etc. - - - The Mica Group - -The micas are very common minerals, easily recognized by their very -perfect basal cleavage, as a result of which thin sheets, often less -than a thousandth of an inch in thickness, readily split off. These are -tough and elastic, which distinguishes mica from the chlorite group in -which there is similar basal cleavage, but the sheets are not elastic. - -Micas are complex silicates of aluminum, with potassium, iron, lithium, -magnesium and hydrogen. They are one of the principle components of many -granites, gneisses, and schists. This mineral is always crystalline, -being in the monoclinic system, but occurring in six-sided prisms. The -cleavage is so dominant a character that the crystal form is usually -overlooked, as it is seldom requisite in determining this mineral. The -size of the sheets of mica depend on the size of the crystals, the -larger sheets expressing great slowness in cooling from the original -magmas. Sometimes the crystals may be two or even three feet in -diameter. The hardness is not great, ranging between 2 and 3. The -specific gravity lies between 2.7 and 3.2. The color varies according to -the composition, from silvery-white, through gray, pink, and green to -black. The luster is vitreous to pearly, sometimes gleaming in the -darker-colored varieties. The commoner types of mica are as follows: - - Muscovite, H₂KAl₃(SiO₄)₃ or potash mica. - Lepidolite, LiK(Al₂OH·F)Al(SiO₃)₃ or lithia mica. - Biotite, (HK)₂(MgFe)₂Al₂(SiO₄)₃ or iron mica. - Phlogopite, H₂KMg₃Al(SiO₈)₃ or magnesia mica. - -Muscovite is colorless, silvery-white, gray or sometimes pale-green or -brown. It gets its name from Moscow where it was early used for window -panes, and it is still used for stove and furnace doors, as well as in -electric work, for a lubricant, etc. - -The best crystals occur in granites, in the coarse varieties of which -large crystals may be obtained. It is found also as small scales in -gneisses and schists, and when weathered from its original rocks it may -be present in sandstones and shales. Muscovite is always in its origin -an elementary component of deep-seated igneous rocks, like granite; but -is never a component of extruded lavas. _Sericite_ is muscovite which -has been secondarily produced by the alteration of other minerals into -muscovite, as when feldspar, cyanite, topaz, etc., have been modified by -the presence of heat and hot vapors, when near lavas that have come in -contact with other rocks. Muscovite is very resistant to alteration by -weathering, but when it does change, the greater part of it becomes -kaolin. It is found at Acworth and Grafton, N. H., in plates, sometimes -a yard across at Paris, Me., Chesterfield and Goshen, Mass., Portland -and Middletown, Conn., at Warwick, Edenville, etc., N. Y., and all down -the Appalachian Mts., also in the Rocky Mts., the Cascade Range, etc. - -Lepidolite is pink or lilac in color and occurs in scaly masses, mostly -in granites. It does not come in large crystals. Lepidolite is found at -Paris and Hebron, Me., Middletown, Conn., Pala, Calif., etc. - -Biotite is dark-brown or black mica. Like muscovite it is very common, -making one of the chief components of granites, gneisses and schists; -and, unlike muscovite, it may occur in extrusive lavas, like trachyte, -andesite, and basalt. It resists weathering much less than muscovite, so -that, when the rocks of which it is a component disintegrate, biotite is -usually altered to kaolin and other compounds. It is likely to occur in -good-sized crystals, especially at Topsam, Me., Moriah, N. Y., Easton, -Penn., etc. - -Phlogopite is pale-brown, often coppery in color, and is most likely to -occur in serpentines, or crystalline limestones or dolomites, often in -fine crystals, of good size. While one of the less abundant micas, this -is found at Gouverneur, Edwards, and Warwick, N. Y., Newton, N. J., and -Burgess, Canada. - - -Topaz -Al₂F₂SiO₄ -Pl. 41 - -Occurs in crystals mostly; hardness, 8; specific gravity, 3.5; colorless -to pale-yellow; luster vitreous; transparent on thin edges. - -Topaz may be colorless, but is more often some shade of yellow, and at -times brown or even blue. Its hardness is characteristic, there being -but few minerals as hard, and it is used to represent the hardness 8 in -the Moh’s scale. The crystals are orthorhombic prisms, with the edges of -the prism beveled and often striated. The ends of crystals usually -terminate with a basal plane, parallel to which there is good cleavage. -Between this basal plane and the prism faces there are usually several -sets of small faces as indicated on Plate 41. - -This mineral, as is also true of most minerals containing fluorine, is -one of those which have crystallized out from hot vapors, escaping from -igneous magmas. It is associated with such minerals, as tourmaline, -beryl, fluorite, and cassiterite, and occurs mostly in cavities or -seams, in or near granites. - -Ordinary topaz, which means crystals that are imperfect by reason of -tiny cracks and impurities is not very rare, but crystals which are -perfect and clear in color are considered gems. Most of the gem-topaz is -some shade of yellow, but may be brown or blue, never, however, pink, as -is often seen in jewelry. The “pinking” is artificial, and done by -packing yellow or brown topaz in magnesia, asbestos, or lime, and then -heating it slowly to red heat, after which it is cooled slowly. If -underheated the color is salmon, if overheated all color disappears. -Topaz has been a gem for centuries, the earliest records coming from -Egypt. The name comes from _topazios_, meaning to seek, because the -earliest known locality, from which it was gathered, was a little island -of that name in the Red Sea, and this island was often surrounded by fog -and hard for those early mariners to find. Here by mandate of the -Egyptian kings the inhabitants had to collect topazes, and deliver them -to the gem-cutters of Egypt for polishing. - -Several yellow stones are called topaz, as the “Oriental topaz” which is -corundum and more valuable than topaz itself; and several varieties of -yellow quartz, which go under such names as “Saxon,” “Scotch,” -“Spanish,” and “smoky” topaz. When topaz occurs colorless as in Siberia, -the Ural Mountains, and in the state of Minas Geraes, Brazil, in all of -which places it is found as pebbles in brooks, it goes under the name of -“slave’s diamonds.” Brazil is today the chief source of gem-quality -topaz. - -Ordinary topaz is found in this country at Trumbull, Conn., Crowder’s -Mt., N. C., Thomas Mts., Utah, in Colorado, Missouri, and California, -etc. - - -Staurolite -FeAl₅OH(SiO₆)₂ -Pl. 41 - -Occurs in orthorhombic crystals; hardness, 7.5; specific gravity, 3.7; -color brown; luster resinous; translucent on thin edges. - -This mineral occurs about equally abundantly in simple crystals similar -to the outline on Plate 41, and in twins which have grown through each -other either at 90° or at 60°. The color is either brown or -reddish-brown. In all cases it is an accessory mineral, occurring in -metamorphic rocks, usually schists, though less frequently in slates and -gneisses. - -From the seventeenth century on, it has been used as a baptismal stone, -and worn as a charm, legends stating that it fell from the heavens. Fine -crystals have been found in Patrick County, Va., and there is in this -region the legend, that when the fairies heard of the crucifixion of -Christ, they wept and their tears falling crystallized in the form of -crosses, such as the one shown on Plate 41. - -Staurolite is found in the schists of New England as at Windham, Me., or -Chesterfield, Mass., and all down the east side of the Appalachian -Mountains to Georgia. - - -Olivine -(MgFe)₂SiO₄ -_Peridot_ or _Chrysolite_ - -Occurs in grains and irregular masses in dark lavas; hardness 6.5 to 7; -specific gravity 3.3; color bottle- to olive-green; luster vitreous; -translucent on thin edges. - -Olivine rarely occurs in crystals, but when it does they belong to the -orthorhombic system. The dark-green grains or masses are recognized by -the color, considerable hardness and indistinct cleavage. Serpentine may -have a similar color, but its hardness is only 4. In hydrochloric acid -olivine decomposes to a gelatinous mass. - -Olivine is typically one of the constituents of the dark lavas, like -basalt, gabbro, or peridotite. It is also a common mineral in -meteorites. Olivine, in the presence of water, alters to other minerals, -especially serpentine, with great facility. - -It occurs fairly widely wherever the dark lavas are present, as in the -White Mountains of N. H., in Loudoun Co., Va., in Lancaster Co., Penn., -and in many localities in the Rocky Mountains and Cascade Range. - - -Epidote -Ca₂(AlOH)(AlFe₂)(SiO₄)₃ -Pl. 42 - -Occurs in grains or columnar masses; hardness, 6.5; specific gravity -3.4; color green, usually a pistachio or yellow-green; luster vitreous; -translucent on thin edges. - -Rarely epidote occurs in crystals, which belong to the monoclinic -system, and may be either short like the diagrams on plate 42 or long -and needle-like. The color and hardness will suffice to determine this -mineral, as almost no other has the peculiar yellowish-green color which -is characteristic of this form. - -Epidote occurs primarily in metamorphic rocks at or near the contact -with igneous rocks; or it may be a secondary mineral resulting from the -weathering of granites, especially along seams. It sometimes occurs with -hornblende in highly folded schists, as in New York City. It is often a -mineral which has resulted from the alteration of other minerals, as -pyroxene, amphibole, biotite, or even feldspars. - -It is found at Chester and Athol, Mass., Haddam, Conn., Amity, Munroe -and Warwick, N.Y., East Branch, Penn., in the Lake Superior region, in -the Rocky Mountains, etc. - - -Tourmaline -(FeCrNaKLi)₄Mg₁₂B₆Al₁₆H₈Si₁₂O₆₃ -Pl. 42 & frontispiece - -Occurs in three-sided prismatic crystals; hardness, 7; specific gravity, -3.1; colorless, red, green, brown, or black; luster vitreous; -transparent on thin edges. - -Tourmaline is readily distinguished from other minerals, as it always -occurs in long to short prisms, which are three-sided in cross section. -There is also a tendency for the sides to be curved as seen on the end -view of D, Pl. 42. Frequently the vertical edges of the prism are -beveled with one, two or three faces, grouped about each of the three -original edges, and there are often striations on the prism faces. The -ends are terminated by a low rhombohedron and again there may be a host -of modifying faces on the edges and corners of the end. The common -varieties are brown or black in color, but occasionally there may occur -green, red, yellow or almost any color. When the crystals are perfect, -that is free from impurities and without tiny cracks, tourmaline becomes -a gem of popularity and value. - -Tourmaline is very complex in composition and may vary considerably, the -sodium, potassium, lithium, magnesium, and iron being either more or -less abundant or even lacking. The color is to some extent dependent on -the proportions of these elements present, the dark varieties having -more iron, and the light colored tourmalines lacking it. This mineral is -one of those which form from superheated vapors, escaping from molten -magmas. It will therefore occur in veins, often associated with copper -minerals, in crystalline limestones, or in cavities in granites, where -it is associated with such minerals, as beryl, apatite, fluorite, topaz, -etc. - -If heated tourmaline crystals develop electricity, with the effect of -making one end a positive and the other a negative pole, and then will -attract bits of straw, ashes, etc. It was first introduced into Europe -about 1703 from India, and its vogue as a gem has greatly increased -since it was found on Mount Mica near Paris, Me. This Paris, Me., -locality was discovered by two boys, amateur mineralogists, Elijah L. -Hamlin and Ezekiel Holmes, who in 1820 were returning home from a trip -hunting for minerals, when, at the root of a tree, they discovered some -gleaming green substance. It proved to be gem-quality tourmaline. A snow -storm that night buried their “claim,” but next spring it was visited -and several fine crystals found. Later this locality was systematically -worked, and over $50,000 worth of tourmaline taken from the pegmatite -seam in the granite, which lay under the crystals found on the surface. -The figure in the frontispiece is one of the crystals from there. - -Well known localities are Paris and Hebron, Me., Goshen and -Chesterfield, Mass., Acworth and Grafton, N. H., Haddam and Munroe, -Conn., Edenville and Port Henry, N. Y., Jefferson Co., Colo., San Diego -Co., Calif., etc. - - -Kaolinite -H₄Al₂Si₂O₉ -_Kaolin_ - -Usually found in whitish clay-like masses; hardness, 2; specific -gravity, 2.6; color white to grayish or yellowish; luster dull. - -Kaolinite does not generally occur in crystals, though crystals of -microscopic size and monoclinic forms have been found. It is a secondary -mineral resulting from the decomposition by weathering of feldspars, the -calcium, potassium or sodium having been replaced by water. When found -in place it is generally white or nearly white, and is characterized by -its greasy feel. - -As granites or other feldspar-bearing rocks are weathered away, the -kaolin is washed out by water, and with other fine material is carried -down into lakes or the sea, where it settles to the bottom and is known -as clay. Clay is kaolin with more or less impurities. - -Pure kaolin is used for the manufacture of china and white porcelain -ware; but when it is impure, especially when it has iron in it, baking -causes the product to turn red or brown, so that it is only suitable for -making tile, bricks, etc. - -It is found almost anywhere that feldspar rocks are, or have been, -exposed to weathering. - - -Talc -H₂Mg₃(SiO₃)₄ - -Occurs in scales, or in fibrous, scaly or compact masses; hardness, 1; -specific gravity, 2.7; color white, gray or pale-green; luster pearly; -translucent on thin edges. - -This mineral is as soft as any, only graphite and molybdenite being of -the same hardness, but both these latter two have a black streak, while -the streak of talc is white. The greasy feel is also characteristic. -Talc is very seldom found in crystals, but if they are found, they will -appear like flakes and have a hexagonal cross section, though in reality -they belong to the monoclinic system. - -Talc is a secondary mineral which usually results from the exposure of -magnesium silicates, such as pyroxenes or amphiboles, to moisture. In -this case, in-as-much as the original rocks were metamorphic in origin, -the talc therefrom will occur in old metamorphic regions. Some talc is -also formed by the action of silica-bearing waters on dolomite. This is -likely to be the case near the contact between dolomite and igneous -rocks. Talc is closely related to serpentine and likely to be found in -the same regions. - -Talc has come to have a considerable use. Some of it is compact and then -called soapstone, and this was used by the ancient Chinese to make -images and ornaments; and our North American Indians used it to make -large pots, to serve as containers for liquids. Some of these pots have -been carved out with great skill, so as to be fairly light in proportion -to what they would hold. Pipes and images were also carved from -soapstone. Today we still cut soapstone into slabs to make mantels, -laundry tubs and sinks. The scaly and fibrous varieties are ground, and -used in making paper, paint, roofing, rubber, soap, crayons, toilet -powders, etc. The United States produce and use over half the world’s -production, our industries requiring over 100,000 tons of talc a year. -Of this 38% goes into paper, 23% into paint, 18% into roofing, and so on -down to toilet powder which uses 2½%, or 2,500 tons a year. - -Talc is found in metamorphosed regions, that is in New England, all down -the east side of the Appalachian Mts., in the Rocky Mts., and the -Cascade Ranges, with a large number of local occurrences. New York State -is the leading producer. - - -Serpentine -H₄Mg₃Si₂O₉ -Pl. 43 - -Occurs in compact, granular or fibrous masses; hardness, 3; specific -gravity, 2.6; color green; luster greasy; translucent on thin edges. -Serpentine is never in crystals. Its color and hardness serve to -distinguish it. Like talc it is a secondary mineral resulting from the -alteration, in the presence of moisture, of pyroxenes, amphiboles, and -especially, olivine. As these are often in metamorphic rocks, the -serpentine is likely to be associated with metamorphic rocks. Some -serpentine is also the result of the action of silica-bearing water on -dolomite, and this is likely to occur in areas of sedimentary rocks. The -fibrous variety of serpentine, _chrysolite_, usually occurs in seams or -veins, and when the fibers are long, it is used as asbestos. This form -of asbestos is the one most used commercially today, as there are -remarkably large deposits of it in the Province of Quebec, which provide -the major part of the world supply. In the United States it is also -found in California and Arizona but only in moderate quantities. - -Massive serpentine is used in considerable quantities as an ornamental -stone, the green color varied with streaks and blotches of white, yellow -and red, due to various impurities, making it very effective. It is, -however, only suitable for interior work as the weather quickly spoils -the polished surface. This is further discussed under serpentine rock, -page 245. - -Serpentine is found at Newfane, Vt., Newburyport, Mass., Brewster, -Antwerp, etc., N. Y., Hoboken, N. J., in Pennsylvania, Maryland, etc. - - -Chlorite -H₈(MgFe)₅Al₂(SiO₆)₃ -Pl. 43 - -Occurs in monoclinic crystals of six-sided outline, or in scaly flakes -or masses; hardness, 2; specific gravity 2.8; color green; luster pearly -on cleavage faces; translucent on thin edges. - -Chlorite is a family name, covering a series of closely related -minerals, so similar in appearance that they are best considered under -this common name. In many respects they resemble mica, in the shape of -the crystals and the remarkable basal cleavage. At first glance it is -easy to confuse the two, but chlorite scales are not elastic, and when -bent, stay bent, instead of snapping back like mica. In fact they look -like more or less rotted micas. This is more than appearance, for -chlorites form as a result of the alteration of micas in the presence of -moisture. They are then secondary, and will be found where mica-rocks -have been weathered, as in granites and schists. - -They may be expected anywhere that micas have been long exposed, as in -New England, the Rocky Mountains, or the Sierra Nevada or Cascade -Ranges. Special localities are Brewster, N. Y., Unionville and Texas, -Penn., etc. - - - The Zeolites - -The zeolites are a group of white minerals, with a pearly luster, light -weight, and easy solubility in acids; which, because their contained -water is lightly held, readily boil before the blowpipe. They are all -secondary minerals, which result from the decomposition of feldspars, -when exposed to weathering. They are almost universally found in seams -and cavities of disintegrating lavas. From a group of a dozen or so, -three are common enough to be considered here. They may be found by -watching such places, as where trap rock is being quarried for road -material, or being blasted for any reason. - - -Analcite -Na₃Al₂Si₄O₁₃ + 2H₂O -Pl. 44 - -Occurs as trapezohedrons in seams and cavities in lavas; hardness, 5.5; -specific gravity, 2.2; colorless, white or pink; luster vitreous; -transparent on thin edges. - -Analcite usually occurs in the 24-sided form, known as a trapezohedron, -as illustrated in figure A, Pl. 44; but it may also occur in cubes with -the three faces of the trapezohedron on each corner. Small crystals are -often colorless, but the larger ones are either white or pink, and are -opaque. While the form is the same as that of garnets, the color, lesser -hardness, and the occurrence in lavas will serve to distinguish this -mineral. If placed in hydrochloric acid analcite dissolves to a -gelatinous mass. - -It is always found in seams and cavities in lavas, as at Bergen Hill and -Weehawken, N. J., Westfield, Mass., in the Lake Superior region, etc. - - -Natrolite -Na₂Al₂Si₃O₁₀ + 2H₂O -Plate 44 - -Occurs as bristling crystals in seams and cavities in lavas; hardness, -5.5; specific gravity, 2.2; colorless; luster vitreous; transparent on -thin edges. - -Natrolite occurs as beautiful bristling tufts of needle-like crystals, -each crystal an orthorhombic prism with a very low pyramid on the end. -This mineral is so easily fusible that it can be melted in a candle -flame, giving to the flame the characteristic yellow color due to -sodium. In hydrochloric acid it dissolves to a gelatinous mass. It is -always a secondary mineral in cavities and seams in disintegrating -lavas, and the tuft-like manner of growth is so characteristic, that -once seen, it will always be recognized. - -Natrolite is found at Weehawken and Bergen Hill, N. J., at Westfield, -Mass., in the Lake Superior region, etc. - - -Stilbite -H₄(CaNa₂)Al₂(SiO₃)₆ + 4H₂O -Pl. 44 - -Usually occurs in sheaf-like bundles of fibrous crystals; hardness, 5.5; -specific gravity 2.2; colorless to white, yellow or brown; luster -vitreous; transparent on thin edges. - -Stilbite crystals are really monoclinic, but on account of almost -universal twinning, appear as if orthorhombic. Like the two foregoing -minerals, stilbite is found in the seams and cavities of disintegrating -lavas. It is readily recognized by its habit of forming in sheaf-like -bundles of fibrous crystals. It may also, but more rarely, occur in -radiating masses. In hydrochloric acid it is completely dissolved. It is -found in lavas, at Weehawken and Bergen Hill, N. J., in the Lake -Superior region, etc. - - - Calcium - -Calcium is one of the most abundant of metals, but never occurs as such -in nature, nor is it used as a metal by man. In its metallic form it is -yellowish-white, and intermediate between lead and gold in hardness. -Exposed to air it soon tarnishes by oxidation, and in water rapidly -decomposes the water, forming the oxide. However, it has a great -affinity for other elements, and makes a large number of minerals, the -most important of which are calcite, aragonite, gypsum and fluorite, -while it is an essential component of some garnets, anorthite, epidote, -amphibole and pyroxene. It is very widely distributed as limestone, and -is found in solution in most all natural waters, and in the shells and -bones of many animals and some plants. - - -Calcite -CaCO₃ -Pl. 45 - -Occurs in well defined crystals in incrustations, and in stalactitic, -oolitic, and granular masses; hardness, 3; specific gravity 2.7; -colorless to white, or when impure, yellow, brown, green, red or blue; -luster vitreous to dull; transparent on thin edges. - -Next to quartz, calcite is the most abundant of all minerals, and occurs -in an almost endless variety of forms, over 300 having been described. -It belongs to the hemihedral section of the hexagonal system, the form -of the crystals being all sorts of variations of the rhombohedron, and -combinations of left and right handed rhombohedrons. The cleavage is -entirely uniform, in three directions, parallel to the faces of the -rhombohedron, and at an angle of 74° 55′ with each other. Crystals may -occur in the form characteristic of the cleavage, but not often. The -commonest forms are a more or less elongated scalenohedron, made by -combining right and left handed rhombohedrons, so that the resulting -pyramid is six-sided, as in figure C, Plate 45. Such a scalenohedron may -be combined with other forms in a great variety of ways. The six-sided -prism with the ends terminated by one or more sets of rhombohedral faces -is also fairly common. Twinning occurs occasionally. - -The quickest way to determine calcite is by the hardness (3), combined -with the fact that it effervesces, when hydrochloric acid is dropped -upon it. - -An interesting feature of this mineral is its marked property of -deflecting light rays, so that a line or object placed behind a piece of -clear calcite appears double. It was with pieces of calcite from Iceland -that this was first seen; so that large transparent crystals of calcite -are still called _Iceland spar_; and such calcite is used to make the -Nichol’s prisms for microscopes, which are so useful in the study of -minerals. This power of refracting light is present in all minerals, but -not to such a marked degree as in calcite. The elongated scalenohedrons -of calcite are often called “dog-toothed spar” from a fancied -resemblance between them and the dog’s tooth. - -Calcite is present in solution in the water of the sea and most streams, -from which it is withdrawn by many animals and some plants, to make -their shells, and bones. The foraminifera, some sponges, the -echinoderms, corals and molluscs all draw large quantities from the -water in which they live, and build more or less permanent structures -from it. These shells when they fall to the bottom, or after being -broken to bits, accumulate on the bottom and make limestone, which is -widely distributed over the country. This same limestone, when -metamorphosed and crystalline, is marble. - -Calcite then is readily soluble in water, and streams flowing along -crevices and fissures in limestone dissolve out great cavities or caves, -like the Mammoth Cave of Kentucky. Other water, percolating through the -limestone, comes to these cavities saturated with lime in solution and -drips from the roofs and walls; then as part of the water evaporates, it -deposits part of its lime in icicle-like masses, hanging from the roof. -Such masses of non-crystalline calcite are called _stalactites_. Below -on the floor of the cave, conical masses are built up in the same manner -where the dripping water falls on the floor. These are _stalagmites_. In -these limestone caves and in smaller cavities many of the most beautiful -crystals grow. Somewhat similarly, when hot water from deep springs -comes to the surface, it cools and can not carry as much lime, and so -around the spring is laid down layer after layer of non-crystalline -calcite making a mass known as _travertine_. Sometimes this is colored -by iron or other impurities and a banded effect results. Such travertine -as the “Suisun marble” from California, “California onyx,” “Mexican -onyx,” and “satin spar” all belong to this class. - -The coral animals, especially in tropical waters precipitate an enormous -amount of lime, until whole reefs are built of lime in this -non-crystalline form. In places it is hundreds of feet thick and -hundreds of miles in extent. Some of this coral has become popular for -personal adornment. This is particularly a small, fine-grained variety, -_Corallum rubrum_, which lives almost exclusively in the Mediterranean -Sea. This coral is red in color, varying all the way from a deep red to -white. It grows in small masses, three pounds being a good sized mass, -in water 60 to 100 feet deep, requires some ten years to develop a -full-sized mass. The making of this into beads and ornaments is an -Italian industry. The demand is growing, while at the same time the -supply is diminishing, and search is being widely made for more such -coral, but up to the present time with little success. This precious -coral is much worn as a protection against the “evil eye” and is widely -imitated, apparently with as much protection to the wearer. When coral -beads are offered cheap, they are probably something else, red gypsum -being much used. This and all imitations can be readily detected by -trying a drop of acid in the bead. Coral will effervesce, but gypsum and -other substitutes will not. - -The bulk of the shells of most molluscs is made of lime, but the -mother-of-pearl layer inside is usually aragonite. The chalk of the -cliffs on either side of the English channel is lime, and composed of -the shells of single celled animals. See p. 213. When lime is deposited -in loose porous masses, as around grass, etc., and below hot springs, -this mass is termed _calcareous tufa_. - -Calcite will be found almost everywhere, some of the localities for the -finest crystals being Antwerp and Lockport, N. Y., Middletown, Conn., -the caves of Kentucky, Warsaw, Ill., Joplin, Mo., Hazel Green, Wis., -etc. - - -Aragonite -CaCO₃ -Pl. 46 - -Occurs in crystals, in columnar or fibrous masses, or incrustations; -hardness, 3.5; specific gravity, 2.9; colorless, white or amber; luster -vitreous; transparent on thin edges. - -Aragonite has the same chemical composition as calcite, but it -crystallizes in the orthorhombic system, either in simple forms like A -on Plate 46, or twinned, so as to make forms which seem hexagonal. When -in simple crystals its form easily distinguishes it from calcite and -dolomite, but when twinned it appears much like either of these two -minerals. From calcite it can then be distinguished by its greater -hardness and the fact that it has cleavage in one direction only, and -that imperfect. The cleavage is the only easy method of distinguishing -it from dolomite. However, aragonite is most always easily distinguished -by its habits, for it generally forms long slender crystals, which -appear more like fibers than crystals. Neither calcite nor dolomite is -at all fibrous. - -Aragonite is much less abundant than calcite, and has resulted, either -from deposition from hot waters, or from waters having sulphates in -solution as well as lime. Much of the travertine, and many stalagmites -and stalactites are composed of aragonites, forming as outlined under -calcite. The mother-of-pearl layer in the shells of bivalves is -generally aragonite. The pearly luster of this layer is due to its being -formed by the successive deposition of one thin layer upon another; so -that light falling on the mother-of-pearl, penetrates, part of it to one -layer and part to another, and is then reflected. Certain molluscs have -this layer composed of especially thin layers, one, the _Unios_ or -freshwater clams, the other, the “pearl oysters” or _Aviculidæ_, these -latter, however, being only distantly related to the edible oysters. In -the cases, where molluscs of either of these two families are of large -size, large pieces of mother-of-pearl can be recovered, and are used for -buttons, handles, and various ornamental objects. A further peculiarity -of these same molluscs is the formation of pearls in the sheet of flesh, -lining the shells. The pearls are round or rounded concretions of -aragonite. At the center there is a grain of sand, or more often a tiny -dead parasite. Either was an irritant to the mollusc, and to be rid of -it, a layer of aragonite was secreted around it. Then as the mollusc -continued to grow and secrete layers for its shell, it also added each -time another layer around the sand-grain or parasite, until in time a -pearl of noticeable, and then of considerable size resulted. These have -all the pearly luster of the mother-of-pearl in a sphere which tends to -make the luster even more marked. - -Pearls were in use as ornaments in China some twenty-three centuries -before Christ, and in India over 500 B.C. They were very highly prized -by the Romans and since their times the rulers of India have shown a -remarkable fondness for them. Today the finest come from the Gulf of -Persia and the Red Sea, while still others are found about Australia and -in the Caribbean Sea. In the United States not a few are collected every -year from the fresh water clams, some of them beautifully tinted with -pink or yellow. - -Aragonite is found widely, as at Haddam, Conn., Edenville, N. Y., -Hoboken, N. J., New Garden, Penn., Warsaw, Ill., etc. - - -Anhydrite -CaSO₄ -Pl. 46 - -Occurs in cleavable or granular masses, rarely in crystals; hardness, -3-3.5; specific gravity, 2.9; color white, gray, bluish or reddish; -luster pearly on cleavage faces; transparent on thin edges. - -When anhydrite occurs in crystals, they are orthorhombic, like the -diagram on Plate 46. Usually, however, it is found in beds or layers, -which were deposited by the evaporation of sea water, and so it is -associated with salt. Anhydrite has three cleavage planes which are at -right angles to one another, which produce rectangular or cube-like -forms. Mostly anhydrite is associated with gypsum, from which it differs -by its greater hardness, pseudo-cubic cleavage, and the fact that -anhydrite is not readily soluble in acid, while gypsum is. Chemically it -differs from gypsum in not having water of crystallization, which gypsum -does have. The anhydrite is likely to occur as veins and irregular -masses in beds of gypsum. Calcium sulphate is precipitated from sea -water when 37% of the water has been evaporated, and it may be deposited -either as anhydrite or as gypsum, the factors, which decide as to which -of these two minerals it will be, being as yet unknown. After -deposition, if exposed to moisture, the anhydrite may change to gypsum, -irregular masses often remaining unchanged. - -It is found in salt mines in Elsworth Co., Kan., in limestone cavities -at Lockport, N. Y., in veins in Shasta Co., Calif., etc. - - -Gypsum -CaSO₄ + 2H₂O -Pl. 47 - -Occurs in crystals, in cleavable masses, or in fibrous masses; hardness, -2; specific gravity, 2.3; colorless, white, amber, gray, or pink; luster -vitreous, silky or pearly; transparent on thin edges. - -Gypsum crystals are monoclinic as seen on Plate 47, the perfect ones -usually occurring in clay, as at Oxford, O., or in cavities; while -crystals of less perfect outline, but with fine cleavages, are found in -Utah, Kansas, and Colorado. The cleavage is very perfect in one -direction, making it possible to strip off thin sheets almost like mica, -and less perfect in two other directions, which appear on the smooth -surface of the first cleavage as lines intersecting at 66° 14′. Twinning -is also common in such a way, that the two united crystals make forms -similar to arrowheads. These cleavages and the twinning show nicely in -the photograph of gypsum on Plate 47. - -Gypsum is distinguished from anhydrite by its lesser hardness, its -cleavage and by being soluble in acids. - -Most gypsum occurs in beds or granular masses which were deposited from -evaporating sea-water, coming down when 37% of the water was lost. Such -beds are often very extensive and are quarried as a source of gypsum to -make plaster of Paris, stucco, neat plaster, Keene’s cement, plaster and -wall board, partition tiles, etc. The use of the gypsum for plaster of -Paris and all these other uses is based on its affinity for water of -crystallization. The gypsum is first heated to about 400° C., which -drives off the water of crystallization, and causes it to crumble to a -powder, which is the plaster of Paris. When water is added, it is taken -up and the powder “sets,” or recrystallizes back to gypsum. This simple -reaction has made it very useful, for making moulds, casts, hard finish -on walls, as stucco, etc. - -When the granular type of gypsum is fine grained, it is known as -_alabaster_, which is used for carving vases, statuettes, ornaments, -etc. The fibrous variety is called _satin spar_, and is sometimes used -for cheap jewelry and ornaments, but it is very soft and quickly wears -out. At Niagara Falls there is a considerable trade in objects carved -from this satin spar, tourists buying them on the assumption that the -mineral is native and comes from under the falls. Most of it, however, -comes from Wales, the small amount of gypsum of that region being mostly -granular. - -Gypsum is found all across the United States, as in New York, Michigan, -Virginia, Ohio, Alabama, South Dakota, Wyoming, Colorado, Utah, -California, etc. - - - The Strontium Group - -Strontium is a pale-yellow metal, ductile and malleable, but oxidizing -quickly when exposed to the air. It does not occur in its native state -in Nature, but always as some compound, usually either the carbonate or -sulphate. It resembles barium, but differs in giving to the flame a -brilliant red color, on which account the compounds of strontium are -used mostly in making red fire in fireworks. - - -Strontianite -SrCO₃ - -Occurs in needle-like crystals, or in columnar or fibrous masses; -hardness, 3.5-4; specific gravity, 3.6; color white, pale-green or pale -shades of yellow; luster vitreous; transparent on thin edges. - -Strontianite is orthorhombic, but appears as if hexagonal, since its -general habit is to have three twin crystals grow together in such a way -as to make a six-sided double pyramid. In this it is very like -witherite, both these minerals appearing externally much alike. They can -be readily distinguished, however, by holding a piece in the flame. If -it gives a red color to the flame it is strontianite, if green, it is -witherite. It effervesces readily in hydrochloric acid. - -Strontianite is found in veins and cavities in limestone, where it has -been deposited after being leached from the limestone by percolating -waters. Though known at several localities it is not now being mined in -this country, what we use being imported mostly from Germany. - -It is found at Schoharie, Chaumont Bay and Theresa, N. Y., in Mifflin -Co., Penn., etc. - - -Celestite -SrSO₄ - -Occurs in crystals, cleavable masses and fibrous; hardness, 3; specific -gravity, 3.9; colorless, white, pale-blue, or reddish; luster vitreous; -transparent on thin edges. - -Celestite, the sulphate of strontium, is very like barite in external -appearance and habit. It is orthorhombic and occurs in tabular crystals. -Its cleavage is perfect on the basal plane, and imperfect in one other -direction. The ready way of distinguishing celestite from barite is to -hold a piece in the flame. If it is celestite it will color the flame -red, if barite, green. - -Celestite is mostly found in veins or cavities in limestone, where it -has been deposited by percolating waters, after having been leached from -the limestone. Some years ago an important deposit of celestite was -found on Strontian Island in Lake Erie, but that was soon worked out and -now no veins are being worked in this country. It is also found at -Chaumont Bay, Schoharie and Lockport, N. Y., in Kansas, Texas, West -Virginia, Tennessee, etc. - - - The Barium Group - -Barium is another metal which does not occur in its native state in -Nature. It has only been isolated as a yellow powder, which, exposed to -air or water, soon changes to one of the oxides. Both barium and its -compounds are peculiar in causing a green color, whenever exposed to the -flame. Two of its compounds are fairly abundant, the sulphate, barite, -and the carbonate, witherite. The former is the more abundant and has -come to be fairly widely used, something over 100,000 tons being -annually consumed in the United States, to make the body in flat finish -paints for interior work and light colors, for a filler in rubber goods, -linoleum, oil cloth, glazed paper, and for a wide range of chemical -compounds. - - -Barite -BaSO₄ -Pl. 48 -_heavy spar_ - -Occurs in crystals or in lamellar, nodular or granular masses; hardness -3; specific gravity, 4.5; colorless, white or almost any color; luster -vitreous; transparent on thin edges. - -Barite occurs in orthorhombic crystals, which are tabular in form, and -usually have the edges beveled, as in figure A, Plate 48. There is -cleavage in three directions, a rather perfect basal cleavage, and two -less perfect cleavages, which are at right angles to the basal cleavage -plane, and intersect each other at 78°. - -The tabular form, the cleavage, the heavy weight, and the fact that a -piece of barite put into the flame colors it green, all serve to -distinguish this mineral. - -Barite is a secondary mineral of aqueous origin, which has been -deposited in veins and cavities in igneous, metamorphic, or sometimes -sedimentary rocks. It is most likely to occur in veins in igneous or -metamorphic rocks, the barium having been dissolved from certain -feldspars and micas by percolating water, and then redeposited in the -fissures, as the water came into them. If in sedimentary rocks, the -barite veins are usually in limestones. Barite is quite likely to be a -gangue mineral for the ores of lead. - -It is found at Hatfield and Leverett, Mass., Cheshire, Conn., Pillar -Point, N. Y., Cartersville, Ga., in Virginia, North Carolina, South -Carolina, Missouri, Kentucky, Tennessee, Alabama, Illinois, Wisconsin, -Nevada, California, Alaska, etc. - - -Witherite -BaCO₃ -Pl. 48 - -Occurs in crystals, or in granular or columnar masses; hardness, 3.5; -specific gravity, 4.3; color white to gray; luster vitreous; translucent -on thin edges. - -Witherite is not an abundant mineral. Its crystals are really -orthorhombic, but they are usually twinned, three crystals growing -through each other in such a manner that the resulting crystal appears -like a six-sided double pyramid, similar to the one figured on Plate 48. -The commonest mode of occurrence is in compact masses. Witherite -effervesces when cold acid is dropped upon it, which, with its heavy -weight, and the green color it gives to the flame, serves to distinguish -the mineral. It is used for medicines, in chemical industries, and a -considerable amount is made into rat poisons. The chief locality for -witherite is in northern England, but in this country it is found along -with barite, especially at Lexington, Ky., and in Michigan. - - - Carbon - -Carbon is an element widely distributed in nature, occasionally -appearing in its elementary form, as graphite or the diamond, but much -more important in its compounds. Small quantities are present in the air -as carbon dioxide, CO₂, immense quantities occurring in the carbonate -minerals, which have been considered under their respective metallic -salts, as calcite, malachite, siderite, cerrusite, smithsonite, -witherite, etc., and still other large quantities being represented in -organic compounds, which occur as rocks under the heads of petroleum, -coal, etc. The occurrence of limestones, graphite, coal or petroleum is -always indicative of the activity of living organisms, and in some cases -is the only indication of life in the earlier rocks. - - -Graphite -C -_Plumbago_ - -Occurs in hexagonal scales or flakes, in layered masses, or earthy -lumps; hardness, 1; specific gravity, 2.1; color black or steel-gray; -streak gray; luster metallic; opaque on thin edges. - -Like the diamond graphite is pure carbon, but in this case it is in -non-crystalline form. It occurs in both igneous and metamorphic rocks. -In the former case it is either in flakes in the rock, or in veins, and -has been derived directly from the molten magmas, having either -precipitated in the hardening granite or lava, or having been carried -into the fissures and there precipitated to make the veins of graphite. -In either case the graphite probably represents organic deposits which -have been melted into the igneous magma at the time of its formation. -Graphite may also occur in metamorphic rocks, beds of coal or other -organic deposits being altered by the heat. Such beds are often of -considerable extent and economic importance. - -The extreme softness, greasy feel, and the dark-gray streak readily -distinguish graphite. - -It is widely used in making crucibles and furnace linings for foundries, -lead pencils, paint, lubricating powders, etc. - -Graphite is found at Brandon, Vt., Sturbridge, Mass., Ashford, Conn., in -Essex, Warren and Washington Cos., N. Y., Clay, Chilton and Coosa Cos., -Ala., Raton, N. M., Dillon, Mont., etc. - - -Diamond -C - -Occurs in octahedral crystals; hardness, 10; specific gravity, 3.5; -colorless to yellow, brown, blue, etc., luster adamantine; transparent -on thin edges. - -Like graphite the diamond is pure carbon, but in this case in crystal -form. It is the hardest of all minerals, and as brilliant as any; so -that in spite of being by no means the rarest, it may easily be -considered the most popular of all gems. Tiny diamonds have been made -artificially under great heat and pressure; so that this mineral is -thought of as forming in Nature in dark igneous lavas at great depths. -The diamond has good cleavage parallel to the octahedron faces, and, in -spite of some traditions to the contrary, is brittle. - -There are not many diamond localities, the most famous being the -Kimberley district of South Africa, which produces many times as many -diamonds as all the others put together, though all the time some are -being found in Borneo and Brazil. A very few have been found in the -United States, only one locality however yielding them in the original -matrix. That is at Murfreesboro, Ark., where they are mined in a -disintegrating peridotite (a dark lava, mostly peridot), which has been -extruded through the sedimentary rocks of that region. This matrix is -similar to the “blue earth,” the matrix of the diamonds of South Africa, -which occurs in “pipes,” representing the necks of ancient volcanoes. -The American diamonds are of small size, averaging considerably less -than a third of a carat in weight, which does not allow great value to -the individual diamonds. - -From time to time, especially large diamonds have been found in -different parts of the world, the largest being the Cullinan diamond, -found at the Premier Diamond Mine of South Africa. It weighed 3025 -carats or about a pound and a quarter, and was valued at over -$3,000,000. It was presented to King Edward VII, who had it cut into 11 -brilliants, four of which are larger than any other diamond yet found. -Other famous diamonds, like the Kohinoor, 106 carats, found in India in -1304; the Regent, 136 carats, also found in India; the Orloff, 193 -carats, set in the eye of an Indian idol; the South Star, 125 carats, -the largest ever found in Brazil; the blue Hope, etc., have in many -cases romantic and interesting stories woven about them. - -Though for ages diamonds have been highly prized gems, it is only in -comparatively recent times that cutting and polishing have been resorted -to, for the purpose of enhancing their brilliancy. This is done by -grinding reflecting faces on the original stone, by the aid of discs of -iron or tin in which diamond dust has been embedded. Diamond chips and -cloudy or imperfect diamonds are used for making tools for cutting -glass, rock drills, etc. - - - Phosphorus - -The element phosphorus at ordinary temperatures is an almost colorless, -faintly yellow, solid substance of glistening appearance and waxy -consistency. In Nature it does not occur pure, but always as one of its -compounds. It is of great importance to man for it is one of the -essentials for plant growth and also for the higher animals, being -required for the bones and to some extent for nervous tissue. Originally -it is found in all the igneous rocks. Some of the phosphorus is removed -by solution and carried to other regions and to the sea. From this -distribution it comes into the sedimentary rocks, and, when they are -altered by heat, into the metamorphic rocks. Thus it has a wide, though -by no means even, distribution. The soils formed by disintegration of -these rocks probably all have some phosphorus in them; but where there -is vigorous plant growth, it soon tends to become exhausted, and must be -renewed. For this reason the use of phosphates has become of prime -importance in Agriculture. The possession of beds of rock carrying -phosphorus has come to be of international importance. The United States -is particularly fortunate in this respect, and produces over 25% of the -world’s supply of phosphates. Most all the phosphorus is recovered -either from phosphate minerals, the most important of which is apatite, -or from the non-crystalline and impure mixtures of phosphate minerals -and other substances, discussed under phosphate rock. - - -Apatite -Ca₅F(PO₄)₃ -Pl. 49 - -Occurs in crystals, concretionary nodules, or in bedded masses; -hardness, 5; specific gravity, 3.2; color reddish-brown or green, rarely -white or colorless; luster vitreous; translucent on thin edges. - -Apatite occurs in hexagonal prisms, usually with the ends truncated by a -basal plane, and with one or more sets of pyramidal faces between the -prism and the basal plane. Crystals range in size from tiny to over a -foot in diameter. There is but one cleavage and that is basal. The -crystal form, cleavage, and hardness will easily determine this mineral. -Apatite is usually associated with igneous or highly metamorphic rocks, -such as granites, gneisses, and crystalline limestones. While the -phosphoric acid of apatite is highly desirable for use in fertilizers, -the crystals do not occur in sufficient abundance to make them -commercially available, and non-crystalline phosphate rocks are resorted -to for this purpose. - -Crystals of apatite are found at Norwich and Bolton, Mass., Rossie and -Edenville, N. Y., Suckasunny and Hurdstown, N. J., Leiperville, Penn., -Wilmington, Del., etc. Templeton, Canada, is perhaps the best known -locality for fine apatite. - - -Turquois -H₅[Al(OH)₂]Cu(OH)(PO₄)₄ - -Occurs in seams and incrustations; hardness, 6; specific gravity, 2.7; -color bluish-green; streak blue; luster waxy; translucent to opaque on -thin edges. - -In this country this complex phosphate of aluminum and copper is found -in streaks and patches in volcanic rocks, but in Persia comes from -metamorphic rocks. To the Persians it was a magical stone, protecting -the wearer from injuries, and among the Pueblo Indians it was regarded -as of religious value in warding off evil. The best turquois comes from -Persia, but it has been found at several points in the United States, as -in Los Cerrillos and Burro Mts., N. M., in Mohave Co., Ariz., San -Bernardino Co., Cal., in Nevada and Colorado. - - - Fluorine - -At ordinary temperatures the element fluorine is a colorless gas, which -was not obtained pure until 1888, because it could not be contained in -vessels of glass, gold, platinum, etc. At that time it was made and kept -in a vessel composed of an alloy of platinum and iridium. Its most -important compound is hydrofluoric acid, a fuming liquid, which is -mostly used to etch or dissolve glass. It occurs in several minerals, -like tourmaline, turquois, etc., but the only one used to obtain the -hydrofluoric acid is fluorite. - - -Fluorite -CaF₂ -Pl. 50 -_Fluor spar_ - -Occurs in crystals and cleavable masses; hardness, 4; specific gravity, -3.2; colorless or some shade of violet, green, yellow, or rose; luster -vitreous; transparent on thin edges. - -Fluorite usually occurs in beautiful cubic crystals, often with the -edges and corners beveled by smaller faces, and occasionally in twins, -which seem to have grown through each other. There is perfect cleavage -parallel to each of the octahedral faces, which often, as in the -illustration on Plate 50, show as cracks cutting off the corners. - -Since fluorite loses weight and color on heating, it is concluded that -the colors are due to the presence of hydrocarbon compounds. The red and -the green fluorite when heated to above 212° F. become phosphorescent, -as may be seen if they are thus heated and exposed to the light, then -taken into the dark. - -Fluorite is quite commonly the gangue mineral associated with metallic -ores, and is also likely to occur with topaz, apatite, etc. It is -generally in such places that it seems to have been deposited from hot -vapors, rising from igneous magmas. - -It is the only mineral at all common from which fluorine can be -obtained, and is used for making hydrofluoric acid, and other chemical -compounds of this element. It is, however, of much greater importance as -a flux in reducing iron, silver, lead and copper ores. In the industries -it finds a place, being used to make apochromatic lenses, cheap jewelry, -and for the electrodes in flaming arc lamps. - -Fluorite is widely distributed, some of the better known localities -being Trumbull and Plymouth, Conn., Rossie and Muscalonge Lake, N. Y., -Gallatin Co., Ill., Thunder Bay, Lake Superior, Missouri, etc. - - -Halite -NaCl -Pl. 50 -_Salt_ - -Occurs in crystals, and in cleavable and granular masses; hardness, 2.5; -specific gravity, 2.1; colorless to white; luster vitreous; transparent -on thin edges. - -Halite is common salt, occurring in cubic crystals, with perfect cubic -cleavage. Its form, hardness, taste, and solubility in water make it -easy to determine. - -Halite is the most abundant salt in sea water, making about 2.5% out of -the total of 3.5% of solids in solution. It is also a prominent, when -not the leading, salt in solution in the waters of inland lakes, like -Great Salt Lake, or the Dead Sea, there being 20% of halite in the -former and 8% in the latter, though the total of solid in solution in -the water of the Dead Sea is greater than that in Great Salt Lake. - -The great salt deposits are mostly the result of the evaporation of the -water of arms or isolated portions of former oceans; the salt, gypsum, -etc., left by the drying sea, having been buried beneath later -sediments. Other bodies of salt represent the disappearance of ancient -lakes. There are also the curious “salt domes” of Louisiana and Texas, -which are immense, roughly circular, subterranean masses of salt -extending to as yet unknown depths which are thought to have been formed -by masses of salt from some deep source bed pushing their way upward -through the overlying formations by plastic flowage. As the upthrust -took place the sediments were arched into domes. Some of these domes are -today important sources of rock salt. - -There are extensive beds of salt under parts of New York, Michigan, -Ohio, Oklahoma, Kansas, etc., which are mostly worked by drilling wells -into the salt layer, then introducing hot water to dissolve the salt. -The brine thus formed is pumped to the surface, and the salt recovered -by evaporation in pans. During the process, skeleton crystals of salt -with concave faces may form, but in Nature the crystals are uniformly -solid cubes. - - -Boracite -Mg₇Cl₂B₁₆O₃₀ - -Occurs in small crystals or granular masses; hardness of crystals, 7; of -the masses, 4.5; specific gravity 3; colorless to white; luster -vitreous; transparent to translucent on thin edges. - -Small crystals, associated with salt and gypsum, occur in the beds and -incrustations, which result from the drying up of alkaline lakes, -especially in Nevada and southern California. The crystals are -orthorhombic, but appear like perfect cubes, with the edges beveled and -part of the corners cut. They are not easily dissolved in water, but -quickly go into solution in hydrochloric acid. - - -Colemanite -Ca₂B₆O₁₁ + 5H₂O - -Occurs in crystals or compact masses; hardness, 4.5; specific gravity, -2.4; colorless to white; luster vitreous; translucent on thin edges. - -The crystals when they occur, are monoclinic; but usually colemanite is -a bedded deposit, which has resulted from the drying up of a saline -lake. It was first found in Death Valley, Cal., in 1882, then near -Daggett, Cal., and since then in several similar locations in Nevada and -Oregon. The deposits are of all grades of purity, the colemanite being -mixed with varying quantities of mud. Today this mineral is the chief -source of borax, which is used in medicines, cosmetics, colored glazes, -enamel, and as a preservative. - - -Borax -NaB₄O₇ + 10H₂O - -Occurs in crystals or in powdery incrustations; hardness, 2; specific -gravity, 1.7; colorless to white; luster vitreous; translucent on thin -edges. - -The crystals are tiny and monoclinic, this mineral being usually -obtained by the evaporation of the saline waters of such lakes as Clear -and Borax Lakes in southern California, or from the muds of salt -marshes, like Searles Borax Marsh in California. Originally most of our -borax came from a large saline lake in Tibet, but now most of it is -obtained from colemanite. Borax is soluble in water, giving it a -sweetish taste. - - -Sulphur -S -Pl. 51 - -Occurs in crystals, incrustations or compact masses; hardness, 2; -specific gravity, 2; color yellow; streak yellow; luster resinous; -translucent on thin edges. - -Aside from the numerous compounds, such as the sulphides of the metals -like pyrite, galena, sphalerite, etc., and the sulphates, like gypsum, -barite, anglesite, etc., sulphur occurs in its elemental form in Nature. -In this case it may be in crystals, which are orthorhombic and usually -occur as octahedrons, with the upper and lower ends truncated, either by -a basal plane, or by a lower octahedron, or by both. Incrustations and -compact masses are, however, much the commoner mode of occurrence. The -incrustations are found mostly about volcanic regions, where the sulphur -has risen from the molten lavas as a sublimate, and on cooling has been -deposited in crevices or on the adjacent surfaces. Irregular masses of -sulphur are often found where sulphide minerals, like pyrite or galena -have been decomposed in such a way as to leave the sulphur behind. The -extensive beds of sulphur are usually associated with gypsum, and are -thought to be the result of water, containing bituminous matter, so -acting on gypsum as to remove the calcium and oxygen as lime, and leave -the sulphur. Finally many waters carry sulphates in solution, from which -the sulphur may be precipitated by certain sulphur bacteria, making thus -incrustations on the bottom of ponds or lakes. - -Sulphur is used for making matches, gunpowder, fireworks, insecticides, -in medicine, vulcanizing rubber, etc. It is widely distributed, however, -most of the present world’s production is from deposits associated with -the “salt domes” of Texas and Louisiana. A “caprock” of gypsum and -anhydrite overlies many of these which often contains elemental sulphur. -Wells are drilled into this, and the sulphur is melted by the -introduction of hot steam. This melted sulphur is then pumped to the -surface and run into molds. - -Some of the best known localities are Sulphurdale, Utah, Cody and -Thermopolis, Wyo., Santa Barbara Co., Cal., Humboldt Co., Nev., and -about the hot springs of the Yellowstone Park. - - -Ice -H₂O -Pl. 51 -_water_ - -Occurs solid as ice, snow and frost, or liquid as water; hardness, 2; -specific gravity, .92; colorless to white; luster adamantine; -transparent on thin edges. - -Though we seldom think of ice, and its liquid form, water, as a mineral, -still it is one, and perhaps the most important of all minerals, as well -as the most common. Ice melts at 32° F. and vaporizes at 212° F., being -then termed steam. Because it is so common and liquid at ordinary -temperatures it acts as a solvent for a host of other minerals, and is -therefore the agent by which they are transported from place to place -and redeposited in veins and beds. - -Not only does water act as a transportation agent for minerals in -solution, but is also the agent of erosion and weathering. Water -vaporizes slowly when exposed to the air at all temperatures above -freezing, and so it is slowly rising from the surface of the sea or -lakes or moist ground into the air, where it would accumulate until the -air was saturated, if the air would only keep still and at a uniform -temperature. The air will hold a given amount of water vapor, which is, -for example, 17 grams per cubic meter when the temperature is 68° F., -but at 59° F. it will hold only 12½ grams, or at 50° F. only 9 grams. -Thus the air is more or less completely saturated at higher -temperatures, and when the temperature is lowered the air can not hold -all it has taken up, and it is precipitated in dew, rain or snow, most -often as rain. When the rain falls it mechanically carries away, and -more or less slowly transports to other places particles of rock, being -thus the agent of erosion; and when it is slowed down, as on entering -the quiet water of a lake or the sea, it drops the mechanically carried -sediment and makes sedimentary deposits. - -Another very important and unique feature of water is that on freezing -it expands about ¹/₁₁th of its former bulk, so that, as a result, ice -floats, and also wherever water in crevices is frozen, the crevices are -enlarged. In locations where this freezing and melting take place -repeatedly throughout a year, there the breaking up of rocks is rapid. - -This is hardly the place to take up a complete discussion of water, but -its action as a solvent, mechanically, and in freezing, melting, and -vaporizing is the basis of a large part of the study of geology. - -When water crystallizes, as in forming ice, it is in the hexagonal -system. It tends to twinning and a snow-flake is made up of a large -number of twinned crystals, each diverging from the other at 60°. When -ice is formed in the air or on the surface of water it forms these -complex and beautiful multiple twins, of which but a couple are -suggested here. Beneath the surface the hexagonal crystals grow downward -into the water, parallel to each other, making a fibrous structure, -which is very apparent when ice is “rotten,” which is the time at which -the surfaces of the prisms are separating, because the molecules leave -the crystal in the reverse order to which they united with it. Frost in -marshy or spongy ground will often show this fibrous growth beautifully. - - - - - CHAPTER IV - THE ROCKS - - -Broadly speaking a rock is an essential part of the crust of the earth, -and includes loose material, like sand, mud, or volcanic ashes, as well -as compact and solid masses, like sandstone and granite. Rocks are -aggregates of minerals, either several minerals grouped together, as are -mica, quartz and feldspar to make granite, or large quantities of a -single mineral, like quartz grains to make sandstone. - -The rocks are most conveniently classified according to their mode of -origin, into three main groups, igneous, sedimentary, and metamorphic. -The igneous rocks are those which have solidified from a molten magma, -like lavas, granites, etc. The sedimentary rocks are those which -represent accumulations of fragments or grains, derived from various -sources, usually the weathering of other rocks, and deposited by such -agents as water, wind and organisms. Metamorphic rocks are those which -were originally either igneous or sedimentary, but have been altered by -the actions of heat, pressure and water, so that the primary character -has been changed, often to such an extent as to be obscured. - -Rocks once formed in any of the above ways are being constantly altered -in character by the various processes of nature. Those exposed on the -surface are weathered to pieces, and the fragments are transported by -wind or water to accumulate elsewhere as sedimentary rocks. Those buried -deep beneath the surface are affected by the high temperature and -pressure of the depths of the earth and thus metamorphosed. For instance -a granite exposed on the surface is slowly weathered, some parts being -carried away in solution by the rain water, others less soluble -remaining as grains of quartz, mica or kaolin. These are transported by -water and sorted, the finer kaolin being carried to still and deep -water, the quartz and mica accumulating in some lowland as sand. This -sand will in time be cemented to a sandstone, later slowly buried -beneath the surface. If buried deep it will feel the effect of the -interior temperature, which increases as one goes down at the rate of -one degree F. for every 50 feet. If this should be in a region where -folding and mountain-making takes place, the material under the folds -would be melted (because of the relief from pressure which would permit -the high temperature to act freely) and become igneous rock, either -coming to the surface as lava, or remaining below the surface and making -a granite or similar rock; while the sedimentary material not melted but -near enough to the molten material to be affected, would be -metamorphosed, in this case to a quartzite. Much of the interest and -profit in studying rocks, will come from the understanding which they -will give as to the history of that particular part of the earth’s crust -where they are found. - - - Igneous Rocks - -Igneous rocks are those which have formed from material that has been -melted, which involves temperatures around 1300° C.; or, if there is -water in the original material, temperatures as low as 800° C. will -suffice. Considering the increase of temperature to be a degree for -every 50 feet downward, this involves the rocks having been at depths of -5 to 10 miles below the surface. While at such depths the temperature -must be high enough to melt rocks, the great pressure of the overlying -rocks seems to keep them solid; for we know that the center of the earth -is solid, as is shown by a variety of observations, such as the rate at -which earthquake waves are transmitted through the earth, the lack of -tidal effects, etc. However, there is every reason to believe that if -the pressure is removed from the rocks which are five to ten miles below -the surface, there is heat enough at those depths to melt them. When the -crust of the earth is folded, as when mountain ranges are formed, the -areas under the arches or upward folds are relieved of pressure. Then -those rocks, which are under the arches and are relieved, become molten. -The molten magma may well up and fill the space beneath the arch where -it would cool again very slowly; or, if there is fissuring during the -folding, some of the molten material may be forced out through the -fissures and pour out over the surface as lava. Another area in which -pressures may be locally relieved is in the region of faulting, where -the crust of the earth is broken into blocks, between which there are -readjustments, some being tipped one way, some another, some uplifted. -Here again there would be areas of relieved pressure and molten magmas -would form, some of them solidifying in place, others rising to the -surface. - -The molten material is termed the magma, and when it reaches the -surface, great quantities of water vapor and other gases escape: or -these gases may even escape from magmas which do not reach the surface, -rising through fissures. As these hot vapors pass through the fissures, -they are cooled, and may deposit part or all of their dissolved -compounds in the fissure, making veins. Lava is the magma minus the -vapors. Magmas vary greatly from place to place, indicating that they -are formed locally and do not come from any general interior reservoir, -as has sometimes been suggested. - -When the molten magmas escape to the surface, they are termed extrusive, -and as they spread out in a layer this is termed a sheet. This rise and -overflow may be quiet, and from time to time one outpouring may follow -another making sheet after sheet. Or after one outpouring, the pressure -below may cease for a time and allow the lava to solidify and make a cap -or cover over the opening. Before more lava can rise, this cover must be -removed. This usually happens in an explosive manner, the lava below, -with the increasing pressure exerted by its expanding gases, finally -exerting enough pressure, so that the cover is broken, or shattered and -thrown in thousands of fragments into the air, as happened at Mt. Pelée -on the Island of Martinique in 1902. The fragments thrown into the air -are often termed volcanic ashes, though this is not a good word for -them, for they have not been burned. - -In case the molten magmas under the relieved areas do not reach the -surface they are termed intrusive. Such magmas may remain in the space -under a mountain fold, or be forced in fissures part way to the surface. -When the magma is forced into more or less vertical cracks and there -solidifies, and these are exposed by erosion, they are termed dikes. -Sometimes the magmas have risen part way to the surface and then pushed -their way between two horizontal layers of rock and there hardened, in -which case they are termed sills, when uncovered. The Palisades along -the Hudson River are the exposed edge of a sill. Again the molten magmas -may well up and spread between two horizontal layers, but come faster -than they can spread horizontally, and then the magma takes the form of -a half sphere, and the overlying layers of rock are domed up over it. -Such a mass is termed a laccolith. In all these cases the mass of -igneous rock is only discovered when the overlying rocks have been -eroded off. The great mass of molten magma under the arches of mountain -ranges simply cools slowly into a granitic type of rock. These masses -are exposed when the thousands of feet of overlying rock are eroded off. -When these masses are exposed, if of but a few miles in extent, they are -called stocks, but, if of many miles in length and breadth, they are -batholiths, and are very characteristic of the heart of mountain ranges. - -In all the above cases the exterior of the molten mass cools first, and -forms a shell around the rest. The shell determines the size of the -mass. As the cooling continues into the interior, it also solidifies, -and as all rocks shrink on cooling, cracks develop, separating the mass -into smaller pieces. There is usually no regularity about these cracks -and the mass is divided into blocks from six inches to three feet in -diameter. However, in some cases, especially in sills and laccoliths -where the cooling is slower, the shrinkage may be marked by a regular -system of cracks which bound the rock into more or less regular -hexagonal columns. The Palisades and the Devil’s Tower in Wyoming (See -Plate 52) show this structure. The Devil’s Tower is the remnant of a -laccolith, all except the central core of which has been eroded away. -All of the above terms have nothing to do with composition, but refer -entirely to the manner of occurrence. - -While the igneous rocks are classified according to their composition, -the rate at which they cooled has much to do with their texture, and -certain names apply to the texture. For instance when the molten lava -cools very rapidly, there is no time for the formation of crystals, and -the resulting rock is glassy or non-crystalline. If the cooling is slow -as in large bodies, crystals have time to form and grow to considerable -size as in granites. Between these all grades may occur; and one -classification of igneous rocks expresses their rate of cooling, in such -terms as the following. - -Glassy—lavas which have cooled so quickly that they are without distinct -crystallization, such as obsidian, pitchstone, etc. - -Dense or felsitic—lavas which have cooled less rapidly, so that crystals -have formed, but in which the crystals are too small to be identified by -the unaided eye, such as felsite or basalt. - -Porphyritic—magmas from which, in solidifying, one mineral has -crystallized out first and the crystals have grown to considerable size, -while the rest have remained small. - -Granitoid—magmas which have solidified slowly, so that all the minerals -have crystallized completely, and the component crystals are large -enough to be recognized readily, as in granite. - -Fragmental—a term applied to the fragments which have resulted from -explosive eruptions of igneous rocks. These fragments may be loose or -consolidated. Volcanic ashes are typical. - -Porous—a term applied to the lava near the upper surface, which is -filled with gas cavities, such as pumice. - -Amygdoloidal—is the term applied to porous lavas, when the cavities have -been filled by other minerals, such as calcite or some of the zeolites. - - -In determining a rock, first decide whether it is igneous, sedimentary -or metamorphic. The igneous character is recognized by its being either -glassy, or composed of masses of crystals irregularly arranged, there -being neither layering nor bedding. - - - CLASSIFICATION OF IGNEOUS ROCKS - - Texture Excess of light colored minerals Excess of dark colored minerals - - Glassy obsidian, perlite, pumice, pitchstone scorias, trachylyte, basalt-obsidian - - Feldspar orthoclase Feldspar Plagioclase No feldspar - Mica and/or hornblende and/or augite Mica and/or hornblende with pyroxene augite and/or hornblende - and/or mica - +quartz -quartz +quartz -quartz +olivine -olivine +olivine -olivine - - Dense rhyolite trachite dacite (felsite) andesite (felsite) basalt augitite or - hornblendite - Porphyritic rhyolite-porphyry trachite-porphyry dacite-porphyry andesite-porphyry basalt-porphyry augitite-porphyry - Granitoid granite syenite quartz-diorite diorite olivine-gabbro gabbro peridotite pyroxenite - Fragmental rhyolite, tuff trachite, tuff Dacite, tuff or andesite tuff or Basalt tuffs and breccias - or breccia or breccia breccia breccia - -When it is located as igneous, turn to the key on page 177 and decide as -to which type of texture is present. If glassy, the color, luster and -type of construction will place it. If the rock is crystalline, first -decide whether feldspar is present, and if present, what type: then -determine the dark mineral, and lastly whether quartz or olivine is -present. In dense rocks the presence of quartz may be determined by -trying the hardness, for none of the other constituents of igneous rocks -have so great hardness. For example, if it is found that a rock is -composed of orthoclase hornblende and quartz, and the texture is -granitoid, it is granite: or if the rock is plagioclase feldspar and -pyroxene of any sort, it is gabbro, etc. - - -Granite -Pl. 53 - -The combination of orthoclase feldspar (or microcline), quartz, and -either mica, hornblende or augite is termed granite, if the texture is -coarse enough so the individual minerals can be recognized with the -unaided eye. The rock is light-colored because the feldspar and quartz -dominate. Accessory minerals may be present such as apatite, zircon, -beryl or magnetite. Varieties of granite are distinguished according to -the dark mineral present. When this is muscovite, it is a -_muscovite-granite_; when it is biotite, a _biotite-granite_; if it is -hornblende, a _hornblende-granite_; etc. The size of crystals in granite -varies widely. When they are as small as ¹/₁₂ of an inch in diameter, it -is termed fine grained; from ¹/₁₂ to ¼ of an inch, it is medium-grained; -when larger, it is coarse-grained. In some cases the crystals may be -over a foot in diameter which is known as _giant granite_. - -Originally granite was a great mass of molten magma, which has cooled -very slowly, having been intruded or thrust up in great stocks or -batholiths beneath overlying rocks, which acted as a blanket to prevent -rapid cooling. These overlying rocks, in their turn, have been acted -upon by the heat and metamorphosed. Granite is particularly likely to -have been formed under mountain folds; so that, after the mountains have -been more or less completely eroded away, the great masses of granite -have come to the surface to mark the axes of the ranges; and even after -the mountains have been wholly worn away, the granite remains to mark -the sites on which they stood. - -In the granite mass itself, there are often veins and dikes, which -probably resulted from the shrinkage of the cooling granite, and they -are filled with a different and usually coarser granite known as -pegmatite. This pegmatite formed from the residual magmatic material, so -that as some of the elements had already crystallized out, the granite -in these dikes is of different composition. The extreme coarseness of -these pegmatites seems to be due to the character of the mineralizing -agents left in the dikes. In some of these pegmatites the feldspar and -quartz are so intergrown, that when broken along the cleavage surface of -the feldspar, the quartz appears like cuneiform characters, and this -variety has been given the name _graphic granite_ (See Plate 53). - -When granite is exposed to weathering, the feldspar is the first mineral -to be decomposed, altering eventually into carbonates, quartz and -kaolin. The dark minerals are only slightly less susceptible and they -break down into carbonates, iron oxides and kaolin. The original quartz -remains unchanged. Of these products the carbonates, some of the iron -oxide and a little of the quartz are carried away in solution. The -kaolin and some of the iron oxide is in fine particles and they are -carried by the water until it comes to the lakes or the sea. The quartz -is left in coarser grains, which are more slowly transported, and -deposited in coarser or finer sand and gravel beds. - -Granites are widely used for building stone, because they can be worked -readily in all directions, and have great strength and beauty. The color -depends largely on the color of the feldspar, which may be white or -pink, in which case the granite will be gray to pink. - -Granites occur throughout New England, the Piedmont Plateau, the Lake -Superior Region, the Black Hills, Rocky Mountains, Sierra Nevada, etc. - - -Syenite -Pl. 54 - -The combination of orthoclase and either mica, hornblende, or augite is -syenite, the texture being coarse enough so that the individual minerals -can be distinguished by the unaided eye. It differs from granite in the -absence of quartz. Syenite is a light-colored rock with the feldspar -predominating. Minerals like apatite, zircon, or magnetite may occur in -it, as accessory minerals. The foregoing would be an ideal syenite, but -usually there is some plagioclase feldspar also present. If this occurs -in such quantities as to nearly equal the orthoclase feldspar, the rock -is termed a _monzonite_; if it predominates, the rock becomes a diorite. -The presence of quartz would make this rock into a granite. Such a -compound rock has its type form, and when the proportions of the -component minerals are changed, it grades into other types. - -Like the granite, syenite is an intrusive rock, which occurs in stocks -and batholiths along the axes of present or past mountain ranges. The -original magma welled up under the mountain folds, where it cooled -slowly, metamorphosing the adjacent rocks. Like granite it has only been -exposed after a long period of erosion has removed the overlying layers -of rock. - -Syenites are not as abundant as granites, but they occur in the White -Mountains, near Little Rock, Ark., in Custer Co., Colo., etc. - - -Quartz-Diorite - -The combination of plagioclase feldspar, quartz and either mica or -hornblende makes quartz-diorite, sometimes called _tonalite_. The above -would be the typical quartz-diorite, but there is usually some -orthoclase present, which if it equals the plagioclase feldspar in -amount makes this into a monzonite; or if it dominates, it makes the -rock a granite. Quartz-diorite is darker colored than the two preceding -rocks, the dark minerals being about as abundant as the light-colored -ones, such as feldspar and quartz. For this reason the weight is also -somewhat greater. - -Like the others this is an intrusive rock, occurring in stocks and -batholiths, and indicative of great molten masses thrust up under -mountain folds, and only exposed after the overlying rocks have been -weathered away. It is by no means an abundant type of rock, but occurs -at Belchertown, Mass., Peekskill, N. Y., in the Yellowstone Park, etc. - - -Diorite - -Plagioclase feldspar with hornblende or mica, or with both, is known as -diorite. It is distinguished from quartz-diorite by the absence of -quartz. There is generally some augite in it, but if this should be -equal to, or exceed the hornblende, the rock is then a gabbro. There may -also be a small amount of orthoclase present, without taking this rock -out of the diorite class, but if the orthoclase feldspar becomes -dominant, then the rock is a syenite. Thus there is gradation into other -groups in all directions. Apatite, magnetite, zircon, and titanite often -occur in small quantities as accessory minerals. Generally the -hornblende is in excess of the feldspar, so that the rock is a -dark-colored one. - -Diorites occur in much the same manner as granites, being in stocks, -batholiths or dikes, and are often associated with granites and gabbros. -They are great intruded masses, associated with mountain making, and -like the preceding rocks, cooled far below the surface, and have been -exposed only after great thicknesses of overlying rocks have been -weathered away. - -Peekskill, N. Y., the Sudbury nickel district in Canada, Mt. Davidson -above the Comstock Lode in Nevada, etc., are typical localities for -finding diorite. - - -Olivine-Gabbro - -The combination of plagioclase feldspar with augite (or any of the -pyroxenes) and olivine makes olivine-gabbro. The feldspar is usually one -of those with considerable calcium in it, like labradorite; and as the -dark minerals predominate, the rock is dark-colored. It is an intrusive -rock, usually in dikes or stocks, where it solidified far below the -surface, and was only exposed after the overlying rocks were weathered -off. It is by no means an abundant type of rock, but is found in the -Lake Superior Region, and near Birch Lake, Minn. - - -Gabbro -Pl. 54 - -Plagioclase feldspar with any one of the pyroxenes, most commonly -augite, is gabbro. There is a wide range in the relative proportions of -the two minerals making gabbro. At one extreme are rocks made entirely, -or almost entirely, of plagioclase feldspar, which are known as -anorthosites, and occur in parts of the higher mountains of the -Adirondacks like Mt. Marcy, in several places in eastern Canada, etc. -Then there are the typical gabbros where the feldspar and augite are -more or less equally represented. At the other extreme come those -gabbros in which the pyroxene predominates, in the most marked cases the -feldspar being entirely lacking, and the rock being termed a pyroxenite. -When the pyroxene of a gabbro is either enstatite or hyposthene (usually -the latter) the gabbro is often called norite. Magnetite, biotite, and -hornblende may occur in small quantities as accessory minerals. - -Gabbro is a common intrusive rock, occurring in stocks, batholiths, and -dikes, and often varies considerably in different parts of the mass. -Like granite the mass solidified far below the surface, under some -mountain fold, and has only been exposed as the result of weathering -away the layers of overlying rock. Gabbros appear much like diorites, -but are distinguished by the fact that the dark mineral is one of the -pyroxenes, instead of an amphibole or a mica. They are widely -distributed, being found in the White Mountains, near Peekskill, N. Y., -Baltimore, Md., about Lake Superior, in Wyoming, the Rocky Mts., etc. - - -Peridotite - -A rock made up of olivine and augite (or any of the pyroxenes) is -peridotite. As it contains no feldspar, and both augite and olivine are -dark-green to black in color, these rocks are always dark green to black -in color and of considerable weight. They are usually rather coarsely -crystalline. Peridotite is usually associated with gabbro, making dikes -which lead from the main gabbro mass. Less frequently it occurs -independently, making up an intrusive mass. Hornblende and mica may be -present in small quantities, as accessory minerals. - -In general these are rather rare rocks, making dikes connected with -stocks or batholiths of gabbro. Peridotite is found near Baltimore, Md., -in Custer Co., Colo., in Kentucky, etc. - - -Pyroxenite - -This represents the extreme among coarsely crystalline igneous rocks, a -whole mass made up of one mineral, and that some one of the pyroxene -group. If the mineral can be exactly determined, the rock may be still -more definitely named. For instance if it is all augite, then the rock -would be called augitite. Like the preceding rocks, pyroxenite is an -intrusive rock, usually found in dikes, which are connected with gabbro, -and it represents the segregation of one mineral out of the gabbro, and -its solidification at one point. Hornblende, magnetite and pyrrhotite -may be present as accessory minerals. This is not a common rock, but it -illustrates the fact that all possible combinations do occur, if the -circumstances have warranted it. It is found near Baltimore, Md., -Webster, N. C., and in Montana. - - -Rhyolite - -This is a combination of orthoclase feldspar, quartz, and either -hornblende, mica or augite in which the crystals are of such small size -that they can not be identified with the naked eye. In composition it -corresponds to granite, but it is much finer in texture. It differs from -trachite by having quartz while the latter has none. This can usually be -determined by trying the hardness as none of the other minerals are as -hard as 7. It is much harder to distinguish it from dacite which differs -only in having plagioclase feldspar in place of the orthoclase, and only -the microscope will enable one to make this distinction. Where the -distinction cannot be made these light-colored lavas are often called -felsite. - -Rhyolite is usually an extrusive lava, occurring in sheets, but -sometimes it is intrusive, occurring in sills, dikes, and laccoliths. In -all these cases the lava has solidified so rapidly, that the crystals -are tiny, and only the general effect of a crystalline structure is -distinguishable. Rhyolites may occur with porphyritic structure, in -which case the presence of the larger feldspar crystals will help to -distinguish whether they are orthoclase or not, making the determination -easier. The color of rhyolites is green, red or gray, always a decided -light shade. - -Rhyolites are abundant in the western states, as in the Black Hills, the -Yellowstone Park, Colorado, Nevada, California, etc. - - -Trachite - -The combination of orthoclase feldspar with mica, hornblende or augite -is termed trachite, if the texture is dense. It is usually an extrusive -lava of light color (green, red or gray), and corresponds in composition -to syenite. It can be distinguished from rhyolite by having no quartz, -and so nothing to show a hardness above 5.5; but it is difficult to -distinguish it from andesite, which differs only in having plagioclase -feldspar in place of orthoclase. It sometimes occurs with a porphyritic -structure, in which case the feldspar crystals are usually large enough -to be distinguished. - -Trachites are not abundant in America, but some are found in the Black -Hills of South Dakota, in Custer Co., Colo., and in Montana. - - -Dacite - -The union of plagioclase feldspar, quartz, and either hornblende or mica -is termed dacite, if the texture is dense. It is an extrusive lava, -occurring mostly in sheets and dikes. It corresponds in composition to -quartz-diorite. As the texture is dense it is difficult to distinguish -dacite from rhyolite, for both have quartz and differ only in the -character of the feldspar, so it is quite common to use the term felsite -which does not distinguish between the two, and only states that the -rock is dense, light-colored and extrusive. When, as often occurs, the -texture is porphyritic, and the feldspars are the large crystals, then -exact determination is fairly easy. - -Dacites are rather common, occurring on McClelland Peak, Nev., in the -Eureka district, Nev., on Lassen’s Peak, Calif., Sepulchre Mt. in the -Yellowstone Park, etc. - - -Andesite - -The union of plagioclase feldspar with mica, hornblende or augite, makes -andesite if the texture is dense. The lack of quartz, and so no mineral -which has a hardness of over 5.5, makes it possible to distinguish -andesite from dacite or rhyolite, but it is hard to distinguish this -rock from trachite, which differs only on having orthoclase feldspar in -place of plagioclase. When the texture is porphyritic and the feldspars -are the large crystals, then it is easy to make the distinction. -Andesite gets its name from being the characteristic lava of the Andes -Mountains, and is the commonest of all the extruded, light-colored -lavas, being the lava of hundreds of flows throughout the western United -States. - -The union of plagioclase feldspar and biotite is the commonest type. -Plagioclase with hornblende or augite is less common, and, when they do -occur, they are usually distinguished as _hornblende-andesite_ or -_augite-andesite_. Magnetite, apatite and zircon may be present as -accessory minerals. - -The lavas of Mt. Hood, Shasta, Rainier and others of the volcanic peaks -of the Cascade Range, those at Eureka and Comstock in Nevada, in the -Yellowstone National Park, and the porphyries of many peaks in Colorado, -like the Henry Mts., etc., which are exposed laccolithic intrusions, are -all andesites, as are many more. - - -Basalt - -The combination of plagioclase feldspar with olivine and augite (or any -other pyroxene) makes a heavy, dark-colored, black to dark-brown rock -which, if its texture is dense or porphyritic, is termed basalt. This -usually has more or less magnetite in it as an accessory mineral, indeed -the magnetite may be so abundant as to be a component part of the rock. -This magnetite makes trouble for anyone trying to use a compass on or -about basalt rocks. These are extrusive or intrusive rocks and -correspond in composition to gabbro. - -Basalts are among the commonest of igneous rocks, and are popularly -designated “_trap_,” much used as a road ballast on account of its -toughness, which is largely due to its dense texture. The coast of New -England is seamed with dikes of basalt, and through the Adirondack and -White Mountains there are a host of these dikes. The crests of such -mountains, as the Holyoke Range, the Tom Range, the Talcott Mts., East -and West Rocks at New Haven, etc., are all basalt sheets. The Palisades, -First Wachung and Second Wachung Mountains of New Jersey are sills of -basalt. The Lake Superior region is crisscrossed with basalt dikes. That -greatest of all lava fields the Columbia Plateau, covering over 200,000 -square miles on the Snake and Columbia Rivers in Oregon, Washington and -Idaho, is all basalt. So it goes all down through Nevada, New Mexico and -California. - - -Porphyry -Pl. 55 - -This is a term which properly refers to texture alone, indicating a -lava, which has cooled in such a manner that one mineral has -crystallized out of the magma first and developed to a larger size, -while the mass of the material formed tiny crystals in which the larger -ones are embedded. The large crystals are technically known as -_phenocrysts_. The surrounding mass of tiny crystals is termed the -_matrix_. This porphyritic structure is especially characteristic of -lavas which have been extruded in large masses, and of intruded lavas in -such places as sills and laccoliths. - -The term porphyry today has the above precise meaning. It is a much -abused word, and has had all sorts of meanings. In the past it was first -used to refer to lavas in general, then it came to be applied to lavas -which had been erupted before Tertiary times, that is to all ancient -lava sheets. This idea soon proved incorrect, lavas being of the same -composition whether ancient or recent. In the West the word is often -colloquially used today to designate almost every kind of igneous rock -occurring in sheets or dikes, if in any way connected with ore deposits. - -When the composition of a rock with porphyritic textures can be -determined, the name due to the composition is coupled with that due to -texture, making such terms as _trachite-porphyry_, _basalt-porphyry_, -etc. - - -Tuff - -Tuff, a term not to be confused with tufa on page 215, is the name used -to designate the finer fragmental ejecta of volcanic eruptions, which -are also often referred to as “volcanic ash,” but the word, ash, conveys -the false impression that the rock is a remnant of something burned, and -is therefore not a good term. When first ejected, tuff is loose -material, but it is usually soon cemented to make a more or less firm -mass of rock, for which the term, tuff, is still retained. In some -cases, while still loose, it is carried by streams to a distance and -deposited in more or less sorted and layered beds: and the finer tuff is -often carried by the winds and laid down, at a considerable distance -from its source, in so called “ash beds.” In both these cases, -sedimentary characteristics have been added to the tuff, and layering -which is characteristic of sedimentary deposits, is present. These -transported tuff beds are really sedimentary, but as there is little -change in the material, they are referred to here and not again. These -tuff beds are not at all uncommon in the sedimentary deposits of -Tertiary age in the Rocky Mountain region. The coarser material of -volcanic eruptions usually goes under the head of breccia. - - -Breccia - -This term is used to describe the coarse fragmental ejecta of volcanic -eruptions. It is also used, in the section under sedimentary rocks, in a -broad sense to include all angular unworn fragmental material, whether -of igneous or sedimentary origin. For this reason, when dealing with -igneous rocks, it is usual to designate the fragments according to their -composition, making such terms as _trachite-breccia_, -_rhyolite-breccia_, etc. - -While still loose (and also even when cemented into beds of rock), it is -customary to designate the smaller fragments, from the size of a grain -of wheat up to an inch or two in diameter, as _lapilli_; the larger -fragments, from two inches up to a foot or so in diameter, as _bombs_; -and the largest masses, often tons in weight, as _volcanic blocks_. - - -Obsidian -Pl. 55 - -Lavas, which have cooled so quickly that crystals have not had time to -form, have a glassy appearance, and are termed obsidian. If the color is -dark, due to the presence of large amounts of those elements which make -dark minerals, this lava is termed _basalt-obsidian_. Obsidian is -characterized by its glassy texture, a hardness around 6, and by -breaking with a conchoidal fracture, so called because the surface is -marked by a series of concentric ridges, something like the lines of -growth on a shell. Obsidians vary greatly in color, but are usually red -or green to black, and translucent on thin edges. While glassy, all the -obsidians contain embryonic crystals, which appear like dust particles -floating in the glassy matrix, or there may even be a few larger -crystals present, which are often arranged in flow lines. Most all large -masses of obsidian have streaks or layers of stony material in them -where crystallization has set in, in a limited way. - -Near the upper surface, obsidians usually have gas cavities scattered -through them, and these may be small and few, or large and numerous. -Indeed the cavities may be so numerous as to dominate and give the rock -a frothy appearance. In this case, if the cavities are small and more or -less uniform, the rock is called _pumice_; if they are larger it is -_scoria_. If, as often happens when the lava is ancient and has been -buried beneath other rocks, the cavities have been filled with some -secondary mineral, then the lava is called an _amygdoloid_. - -Obsidian is found in many localities, especially where there are recent -volcanoes, the most famous places being the obsidian cliffs in the -Yellowstone Park, those near Mono Lake in California, and many other -localities in the Rocky Mountains, the Sierra Nevadas, and the Cascade -Mountains. - - -Pitchstone - -This is very like obsidian in appearance, but differs in that the glassy -material contains from five to ten per cent of water in its composition, -the most obvious effect of which is to make the luster resinous, instead -of vitreous, as is characteristic of obsidian. The colors are commonly -red, green or brown. Pitchstone is associated with recent volcanoes, and -some fine specimens have come from Silver Cliffs, Colo., and various -parts of New Mexico and Nevada. - - -Perlite -_pearlstone_ - -Perlite is a glassy lava, containing two to four per cent of water, -which, on cooling, has cracked into numerous rounded masses, with a -concentric structure, reminding one of the layers of an onion. - - -Scoria - -While lava is cooling, there is a constant escape of gases, mostly -steam, and as these rise through the molten mass they make cavities, -near the upper surface, that portion on top often becoming frothy. If -this solidifies quickly so that the gas cavities are preserved it is -scoria. When the gas cavities are small and uniformly distributed, the -rock is called pumice, and often used as a scouring agent. When the -cavities are large and irregular the term scoria is generally used. -Molten lavas may form various structures, according to the conditions -under which they cool, dripping through cracks or from the roof of -caves, which often form where the molten lava escapes from a hardened -shell, and making stalactites, stalagmites, etc. The very thin lava of -the Hawaiian volcanoes may even be blown by the wind into fine threads, -known as “Pele’s hair.” - -The presence of the gas cavities is so characteristic of the upper -surface of lavas which have been extruded; that, where one is dealing -with older lavas, now buried beneath other rocks, this fact helps to -determine whether the mass is a sheet, rather than a sill; for, in the -case of the sill, the lava was forced between layers of sedimentary -rocks, and the burden of the overlying rocks did not permit the escape -of steam and therefore the upper surface of sills does not have the -scoriaceous structure. - - -Amygdoloid -Pl. 56 - -When the upper surface of a lava is filled with steam holes, and this -lava has been buried beneath other rocks, the seeping waters slowly -bring such minerals as quartz, calcite and zeolites and fill the -cavities. Such a rock is known as an amygdoloid. It is often confused -with porphyry; but, if examined closely, it will be seen that the -outlines of the gas cavities are rounded, while the outlines of a -crystal, like a phenocryst, are always angular. This will be clear if -the amygdoloid on Plate 56 is compared with the porphyry on Plate 55. - - - The Sedimentary Rocks - -To this class belong all those rocks which have been laid down by water -or wind, or are the results of organic depositions. They include loose -material like sand or day, and also the same materials, when cemented -into more or less solid rocks, like sandstone or shale. So long as the -material has not been altered from what it was when laid down, the rock -is termed sedimentary. - -In general the material of which these rocks are composed comes from the -weathering and disintegration of other rocks. This does not apply to the -organic deposits, for each type of which there is a peculiar mode of -formation. To illustrate the typical formation of sedimentary rocks, we -may look at the fate of a granite when exposed. At once the surface is -attacked by changes of temperature, frost and rain. The various minerals -of the granite expand and contract with every change of temperature, but -each component mineral has a different coefficient of expansion under -heat, so that minute cracks are quickly formed between the minerals. -Water gets into these cracks and begins to dissolve the minerals. -Feldspar is the most easily attacked, part of it being dissolved and -carried away, a small part changing to quartz, and by far the largest -part changing to kaolin. The dark mineral is also attacked and partly -dissolved, and partly changed to kaolin and iron oxides. The quartz -resists solution almost completely. Of these products the kaolin and -iron oxides are carried far away and deposited in still water. The -quartz and perhaps some of the dark mineral are heavier and carried more -slowly, being deposited as sand. This happens to granite everywhere, but -in the regions where there is frost the action is greatly hastened; for -water gets into the cracks and expands every time it freezes and thus -widens the cracks rapidly, which greatly facilitates the entrance and -movement of water in the rock. In a similar way any original rock will -be disintegrated, and the residue, after the soluble part has been -carried away, becomes sand or clay or mud. - -Particles of quartz, kaolin, and lime, separately, or mixed, loose or -more or less cemented, with accompanying impurities, make up the great -bulk of the sedimentary rocks. They are usually arranged in layers, of -varying thickness, as they were laid down by water or the wind. In the -same way layered accumulations which are either products of plants or -animals, or parts of the plants or animals, are considered sedimentary, -as for instance, coal, chalk, petroleum, etc. - - - A Classification of Sedimentary Rocks - - Inorganic origin: - 1. Coarse fragmentary material talus - resulting from weathering - 2. The same fragmentary material breccia - cemented - 3. Unsorted material resulting from soil - rock weathering - 4. Coarse fragments rounded by the gravel - action of water and wind - 5. The same material cemented conglomerate - 6. Finer material deposited by water sand - or wind - 7. The same material cemented sandstone - 8. The finest material, mostly clay - kaolin, deposited by water - 9. The finest material, deposited by loess - wind - 10. The same material cemented shale - 11. Fine particles of lime, pure or marl - impure - 12. The same material cemented limestone - 13. Unassorted material left by the till - glacial ice - 14. The same material cemented tillite - Organic Origin: - 15. Limes made from shells, etc. coquina, chalk, coral rock, - etc. - 16. Silica from the shells of plants, diatomaceous earth, etc. - etc. - 17. Carbon from plants peat, lignite, coal, etc. - 18. Hydrocarbons from animals petroleum, asphalt, amber, - etc. - 19. Phosphates from animals guano, phosphate rock, etc. - - -Talus - -Where weathering is very active, especially on or below steep mountain -slopes, a mass of loose, angular fragments accumulates. This material is -termed talus, a term which refers only to the physical character of the -material, and not at all to its composition. If weathering continues -these fragments will be further broken up into one of the finer grained -rocks, which the water can carry away and deposit elsewhere. There is -little or no layering in talus. If the talus is not carried away but is -cemented where it was formed, the resulting mass is termed breccia, but -this is not very commonly the case. - - -Breccia -Pl. 58 - -The term breccia is used to cover all those rocks which are composed of -angular fragments, of any composition, and above sand in size, when they -are cemented into a solid mass, by any sort of cementing agent. Here the -term is used in its broad sense, as compared with the way it was used -under igneous rocks. - -Breccias may result from the cementing of talus, but more often the -breaking up of the material into angular fragments was due to other -causes, such as crushing along a fault plane, or in the movements -involved in mountain making. In such cases the breccia is of limited -extent, but may occur repeatedly in the same neighborhood. Limestone, -which has been crushed and then recemented, often makes a rock which -takes a good polish and is used in several localities as an ornamental -stone in place of marble, in fact often goes in trade circles under the -name of “marble.” The breccia figured on Plate 58 is such a limestone. - - -Soil - -Over most of the earth’s surface there is a covering of rock waste, the -product of weathering, some of which is unassorted, and some of it -sorted by water or wind. This is all termed soil. It is an ever-moving -cover resulting from the decomposition of the underlying rocks, to which -have been added in places layers of rock waste brought from afar by the -streams. Some soils are rock waste which had been carried clear to the -ocean and deposited on the floor of the sea, and is now above sea level, -because the floor of the sea has been elevated. Inasmuch as the -underlying rocks vary in composition, and as there are areas of -transported material, it is clear that the composition of soils must -vary from place to place, both as to composition and texture. - -Soils range from the finest, composed mostly of clay, to coarse ones, -composed of sand, gravel or even boulders. Clay, the finest grained -soil, is composed of particles only about ¹/₁₀₀₀th of a millimeter in -diameter, of which it would take 720,000 billion particles to make a -gram’s weight. Ordinary soils however have about 2 to 5 million -particles to the gram. - -The average specific gravity of soil with the usual amount of humus in -it is from 2.55 to 2.75. In this case however the specific gravity is of -less importance than is the volume weight. A cubic foot of water weighs -62½ pounds, that of soil from 75 to 80 pounds, the extremes being 30 lb. -for peaty soil and 110 lb. for calcareous sand. The terms “heavy” and -“light,” used in agriculture do not refer to the volume weight, for clay -which is actually relatively light (70-75 lb. per cubic foot) is classed -as a “heavy” soil; while sand, of much greater actual weight, is classed -as a “light” soil. These terms as used in agriculture refer to the ease -with which the soils are worked, and to their penetrability by plant -roots. - -Soil is usually divided into an upper darker-colored layer, termed loam, -and into a lower, lighter-colored layer, termed subsoil. The presence of -humus, resulting from the decomposition of plant and animal remains is -the factor which darkens the color and distinguishes the loam; so that -loam is a complex of inorganic rock particles plus more or less humus, -colloid compounds, bacteria, living plants and animals. The subsoil is -mainly rock particles. The distinctions between these two layers break -down in arid soils, and often also in swampy regions. - -It is this layer of soil on which the water of every rain and flood -works, picking part of it up and carrying it along, step by step, to the -sea. Though the amount moved on any one day is small, the sum of all the -soil transported is enormous, a large river carrying annual incredible -amounts. For instance the Mississippi annually deposits in the Gulf of -Mexico 476,900,000 metric tons (2204 lb. to the metric ton), of which -about a third is in solution. At this rate it takes about 7000 to 9000 -years to remove a foot from over the whole drainage basin. This is -considerably slower than is the case of some other rivers. While on the -one hand soil is being continuously carried away from the surface, on -the other hand it is being constantly renewed from below, by the -weathering action of water, air and temperature. - - -Gravel - -Gravel is a mass of loose fragments of rock, which have been rounded by -water and deposited with little or no sorting, so that larger and -smaller pebbles and sand all occur together. It is the deposit laid down -by comparatively fast water in inland lakes or along the storm-beaten -shores of the sea. Where a swift stream enters quiet water, as where it -empties into a lake, there it quickly drops its coarse material as -gravel, usually thus building a delta. Gravel also occurs in stream -beds, where for any reason the rate of flow is checked. During the -recent glacial period, the ice sheet brought down great masses of -unsorted material, which was deposited as till, or in moraines. Much of -this was then picked up by the running water and moved longer or shorter -distances, so that, all over the glaciated country of the northern and -eastern United States, there are unusually large numbers of gravel -deposits. Gravels are all water laid, and usually show more or less -clearly the bedded or stratified structure. - -The size of the component pebbles of gravel ranges from great boulders -to fine sand, and the finer gravels grade into the coarser sands, the -line between gravel and sand being drawn at about the size of a pea, the -coarser being gravel, the finer sand. - -Gravel is widely used as ballast for railroads and in making highways, -because of its tendence to pack well, while the hard pebbles resist -wear. It is also widely used in concrete work, bonding in well with the -cement, and making it go from three to five times as far. - - -Conglomerate -Pl. 58 - -Conglomerates are composed of rounded pebbles and sand of varying sizes, -cemented together into a solid rock. The pebbles may run up to boulders -in size, but they have all been more or less rounded by water, and -transported some distance. The pebbles may all be of the same -composition, or may represent a variety of rocks. When the pebbles are -all, or most all, of one sort, the resulting conglomerate is termed a -_quartz-conglomerate_, a _limestone-conglomerate_, a -_gneiss-conglomerate_, etc. So too the cementing material varies in -kind, silica, calcite and iron oxide being the commonest. The color will -depend on both the component pebbles and the cement, sometimes one -dominating, sometimes the other. There are some of the quartz- and -limestone-conglomerates which can be cut and polished to make very -handsome stone. - -Conglomerates represent consolidated gravels, and always indicate an -aqueous origin, quite often the delta of an ancient stream, or the -invasion of the sea over the land; so they have become of importance to -geologists in interpreting past events. - - -Sand - -Sand is a mass of small rock particles, from the size of a pea down to -¹/₅₀₀ of an inch in diameter. The material may be any sort of rock, or a -mixture of two or more kinds. Sand may be the result of the -disintegration of older rocks at the point where it is now found, in -which case the grains have the shapes they had in the original rock; but -more often the sand grains have been transported greater or lesser -distances, and in the process have been more or less rounded. - -Those sands, which lie where they were formed are called _residual_, and -such sand is usually composed of a mixture of angular grains, some -harder and others softer, such as quartz, feldspar, mica and hornblende, -all mixed together. Where the sand has been transported, only the more -resistant minerals have remained, such as quartz, magnetite, -cassiderite, etc.; with which there are at times rarer minerals, such as -gold, platinum, garnets or topaz. Such sands are known as -_gold-bearing_, _topaz-bearing_, etc. - -The sands from different localities differ greatly. The streams gather -the rock particles, and sort them according to the size, which the water -flowing at any given rate can carry. When the water is slowed down, it -drops all the particles above the size which the new rate of speed can -handle. The grains of sand from the bed of a stream are usually more or -less angular. The further they are carried, the more they are knocked -together and rounded; so that after being carried to the sea, and then -thrown up on the beaches, they have been well rounded, especially the -larger grains. As the air is less viscid than the water, sand which is -transported by the wind, is even more rounded; so that desert sands show -the most complete rounding, indeed are even polished; and this is true -even of the smaller grains. It is the wind-blown, or desert sands, which -flow so evenly in an hourglass. Between the angular residual sands and -the polished desert sands, there are of course all grades. Glacial sands -are angular or “sharp” almost to the degree characteristic of residual -sands; and lake-shore sands are between river sands and sea sands in the -degree of rounding. - -Sands made of particles of lime, _calcareous sands_, are less resistant -to wear than are those of quartz. In regions where the water is “soft” -(free from lime), they do not last long, as they are dissolved; but in a -limestone region where the water is “hard” (saturated with lime), the -grains are not so quickly dissolved and may accumulate into beds of -great thickness, as in Florida. Along some shores of the ocean, there -occur “green sands,” which are ordinary quartz sands mixed with the dark -green mineral glauconite, which is a potassium iron silicate, forming on -the ocean bottom as a result of the action of decaying animal matter on -iron-bearing clays and potassium-bearing silicates, like feldspar. This -is particularly characteristic of some of the sands along the coast of -New Jersey. - -In places, especially in the beds of rivers, there occur “quicksands.” -This is a deposit of fine sand, mixed with a considerable amount of -clay, and saturated with water; so that it will not support the weight -of a man or an animal. Much that goes under the name of quicksand is a -fluid mud, covered with a thin layer of sand. - -Sand is used for a wide variety of commercial purposes, and under these -conditions gets various trade names; for instance “glass sand” is a -pure, colorless to white, quartz sand, which is used as one of the -components in making glass. It must be free from impurities, as these -color the glass, and much of the sand used for this purpose is quartz, -crushed to a fine sand-like condition. “Moulding sand” is a rather -fine-grained quartz sand, with a small but very definite admixture of -clay, and this is used to make the moulds for castings in foundries. -“Polishing sand” is one composed of angular fragments of quartz, usually -from stream beds or glacial deposits, or even crushed quartz, and is -used for cutting and polishing marble, for sandpaper, and for polishing -wood and softer stones. There are many other special uses, like -building, ballast, filters, furnaces, etc., in which quartz sand is -used, being screened if necessary to get the right sizes. - - -Sandstone - -When sand of any sort is cemented so as to make a solid rock, it is -termed sandstone, which varies widely according to the size, color and -composition of the grains, and also with the sort and amount of the -cement. When the size of the grains is larger than that of a pea, -sandstone grades into conglomerate; when smaller than ¹/₅₀₀th of an -inch, especially if mixed with clay, it grades into shale. There are all -grades of firmness, due to the amount and kind of cement, ranging from -those which have little or no cement, but are compact as a result of the -pressure of the overlying rocks, to those in which the cement has filled -all the pore spaces. In general there is a considerable amount of space -between the grains of sand; so that a sandstone will absorb large -amounts of water, up to 25% of its bulk. In moist climates where it -freezes, this makes many sandstones unsuitable for use as building -stones, as they are likely to spale, or chip off, as is seen in the -“brown stone” so much used in New York City. - -Sandstones are usually bedded rocks and are relatively easy to quarry, -and most of them are not so firmly cemented, but that they can be -readily worked or cut into shape by the stone cutter; and so, certain -sandstones are very popular for building stone or for trimming on -buildings, where they are not too much exposed to the weather. - -Sandstone gets a variety of names according to the cement. - -Siliceous sandstone is cemented with silica and usually very hard. - -Calcareous sandstone is cemented with lime and usually rather soft. - -Ferruginous sandstone is cemented with one of the iron oxides. - -Argillaceous sandstone is held together with clay impurities, and is -usually both soft and of undesirable color. - -According to their composition there is also a number of varieties. - -Arkose is a sandstone composed of quartz and feldspar grains, usually -derived from the disintegration of granite and not transported far. - -Graywacke is a sandstone composed of quartz, feldspar, and some other -mineral, like hornblende-augite, etc., also derived from the -disintegration of granites and not transported far. - -Grit is a term applied to a coarse sandstone, composed of angular quartz -fragments, and used to a considerable extent for millstones. - -Flagstone is a thin bedded sandstone, often with mica, which splits -easily and uniformly along the bedding planes; so that it can be -quarried in large slabs. It was widely used for sidewalks before the -advent of concrete. - -Freestone is a thick-bedded sandstone, not over hard, so called, because -it can be worked freely and equally well in all directions. - - -Clay - -Clay is a term used to describe a mass of fine particles, the most -prominent property of which is plasticity when wet. Clays range from -masses of pure kaolin to masses of kaolin and related minerals mixed -with as much as 60% of impurities, which may be sand, lime, iron oxides, -etc. The particles of a fine clay range around ¹/₁₀₀₀ of a millimeter in -diameter, while the impurities may be, and usually are, of larger size, -up to the size of sand grains. - -All clays are of secondary origin, the result of weathering, especially -of feldspars, though clays may also result from the weathering of -serpentines, gabbros, etc. In some cases after the weathering of -feldspar or limestones, the clay may remain just where it was formed, as -a residual deposit; but, being so fine-grained, it is usually -transported by rain water or by the wind and deposited somewhere else as -a sedimentary bed. The quiet waters of a lake are favorable places for -such deposits, and many clay beds represent former lake bottoms. Impure -clays are often laid down on the flood plains of sluggish streams. In -fresh water the settling of the clay is a very slow process, requiring -days, or when very fine, weeks, before the water wholly clears. In salt -water, however, the clay sort of coagulates, the particles gathering -together in tiny balls, which settle rapidly, so that the water is soon -clear. - -According to their mode of origin clays are classified as residual, -sedimentary, marine, swamp, lake, flood-plain, eolian, etc. But when -their uses are considered a very different classification is made, based -mostly on their composition, and we speak of China clays or kaolins, -fire or refractory clays, paving-brick clays, sewer-pipe, stone-ware, -brick, gumbo and slip clays. - -The kaolin or china clays are residual clays, usually resulting from the -decomposition of pegmatite dikes. They must be white when burned, free -from iron oxides, and fairly plastic. A good deal of china clay is made -by crushing feldspar. - -Ball clays are sedimentary clays which remain white when burned, are -usually very plastic, and free from iron oxides. They are mostly used in -the making of various sorts of china. - -Fire clays may or may not have iron oxides in them, but they must be -free or nearly free from fluxing materials, such as lime, magnesia and -the alkalies (sodium and potassium compounds). They may be more or less -plastic, the essential quality being their ability to withstand high -temperatures without fusing. Silica (as sand) tends to diminish the -refractory quality; so that a clay otherwise suitable, if it has sand in -it, becomes at best a second grade fire clay. In coal mining sections it -is customary to term those beds of clay either above or below the coal, -“fire clay”; but this is an unfortunate designation, for though some of -them are true fire clays, the most of them are not. - -Stone-ware clays are those with considerable sand and up to five per -cent of fluxing materials. They must be plastic enough to be readily -worked, and then burn to a dense body at comparatively low temperatures. - -Sewer-pipe clays must be plastic, and carry a considerable amount of -fluxing material, as the surface of the pipe is expected to vitrify in -the burning. - -Brick clays are low grade clays and vary greatly in composition. The -main requisites are that they mould easily and bake hard at relatively -low temperatures with as little warping and cracking as possible. As -most clays shrink both in the air drying and in the baking, sand is -added when the clay is being mixed. The color is mostly due to the -presence of iron impurities. If there are iron oxides and little or no -lime, the brick bakes to a red color, but if there is an excess of lime -over the iron oxides, it bakes to a cream or buff color, which on -vitrifying turns green. - -Paving-brick clays range from surface clays, to semirefractory clays, -shale being often used. The essential component is enough fluxing -material, so that the bricks shall begin to vitrify, or fuse, at not too -high temperatures. - -Slip clays are those with a high percentage of fluxing material; so -that, when baked at moderate temperatures, the surface fuses into a -glassy brown or green glaze. - -Adobe is an impure calcareous clay, widely used in the western United -States for making sun-dried bricks. - -Gumbo is a term applied to fine-grained plastic clays which shrink too -much in the burning to be useful in manufactures. They can be burned to -make an excellent ballast for railroads and highways. They are -especially abundant in the Middle Western States. - - -Loess - -This is the name given to a fine grained homogeneous clay-like material, -which is a mixture of clay, fine angular fragments of sand, flakes of -mica and more or less calcareous matter. It is usually without -stratification, and cleaves vertically, so that, when eroded, it forms -steep cliffs. Loess covers great areas in the Mississippi Valley, in the -Rhine Valley, and in North Central China. By some it is thought to be an -accumulation of dust in those regions where the prevailing winds were of -diminished velocity and where the grass or other vegetation has served -to catch and hold the material; by others it is thought of as a river -and lake deposit; and by still others it is thought to be due to the -combination of the two modes, wind and flood. The writer inclines to the -first view expressed. - - -Shale -Pl. 59 - -When pure or impure clays, or loess, are consolidated, they are all -grouped under the name shale. It usually possesses a layered or -stratified structure, which makes it possible to split it into thin -layers. Of all the sedimentary rocks shale is the commonest, and it may -occur in all the places where clay could occur, but the most widely -distributed shale is that which made the sea bottom of former times and -is more or less calcareous, like the piece on Plate 59, in which bits of -shells are still visible. Shale has the same wide variation in -composition as has clay, the various types being designated according to -the impurity which is present, as: - -_argillaceous shale_, made mostly of clay, - -_arenaceous shale_, shale with more or less sand as an impurity, - -_calcareous shale_, or one with more or less lime as an impurity, - -_ferruginous shale_, or one with iron compounds as impurities, - -_bituminous shale_, or one colored black by the presence of organic -matter, remains of either plants or animals. - -While of no value as building material, shale may be ground or crushed, -and used as a substitute for any corresponding clay, and thus many -manufacturers use shale in making fire-clay products, bricks, tile, etc. - - -Marl - -Where limestones or shells of any sort have been pulverized, and mixed -with more or less impurities, especially clay, the resulting -unconsolidated mass is known as marl. It is usually associated with -marine formations, and is the finer débris which has settled on the -ocean bottom well out from shore, that is out beyond the sandy and mud -deposits. Finding it therefore usually indicates a sea bottom recently -elevated. It is very characteristic of the southern coastal states, from -Maryland all along to Texas. - - -Limestone - -Any mass of marl, or aggregate of calcareous shells, corals, etc., which -has become consolidated is known as limestone. It may, and usually does, -have a wide range of impurities, chief of which are clay, sand, iron -oxides, and bituminous matter, like plant or animal remains. Pure -limestone is white, but due to impurities it ranges through grays, -greens, browns, to black, and even red, but this last is rarer. It is -easily identified by the presence of calcium carbonate, which -effervesces in hydrochloric acid. It most often represents deposits in -fairly deep water on ocean bottoms of the past, but there is also a wide -range of limestones which were formed in fresh water. - -Limestone is often burned at temperatures just above 900° C, at which -point carbon dioxide goes off as a gas, and leaves calcium oxide, or -lime. When this is mixed with water it makes calcium hydroxide, or -slaked lime, which is mixed with sand to give it body, and is used as -mortar. When exposed to the air, the slaked lime gives up water, and -takes back from the air carbon dioxide, and again becomes calcium -carbonate with its original hardness. Limestone is also used as one of -the elements in all cements. It is also considerably used as a building -stone, which, however, suffers in moist climates from the solution of -its lime by rains, but has stood up very well in dry climates. - -The varieties of limestone are mostly distinguished according to their -mode of origin, some of them being as follows. - -Bog Lime is a white calcareous powdery deposit on the bottom of ponds in -limestone regions, a deposit precipitated from solution by the action of -the plants inhabiting the ponds. - -Coquina (Plate 59) is the rock formed by the rather loose consolidation -of shells and shell fragments. It is particularly characteristic of -tropical regions, and is very abundant near St. Augustine, Fla., in -which region it was, and still is, cut into blocks and used for building -stone. In that mild climate it has stood very well. - -Chalk (Plate 60) is a soft fine-grained limestone, formed in the ocean -by the accumulation of myriads of the tiny shells of Foramenifera, which -are single celled animals, living either a floating life near the -surface of the sea, or a creeping life on the bottom. Chalk is composed -mostly of the shells of floating Foramenifera, which when the animals -died, settled to the bottom and there accumulated, mostly at depths of -600 feet or more. When the mass of unconsolidated shells is dredged up -from depths of 50 to 2000 fathoms, it is known as _Foramenifera ooze_. -Chalk beds are then indications of an uplifted sea bottom. When -consolidated, if pure or nearly so, it makes a white chalk, and the beds -may be of considerable thickness, as is the case of the famous cliffs -near Dover on either side of the English Channel. One of Huxley’s most -famous lectures is the one on chalk, found in his _Essays and Lay -Sermons_. - -Coral Rock is made by the cementation of fragments of corals. The -binding material, as in most stones, is lime; and this sort of rock is -associated with coral reefs of either the past or the present. One of -the best illustrations of this being the “Dolomite Mountains” in Tyrol. -Coral rock, like coquina, has been cut into blocks and used as building -stone, as in Bermuda. - -Encrinal Limestone (Plate 60) is a rock made by the cementation of -fragments of the skeleton of crinoids. These animals belong to the -group, echinoderms, and are now extinct except for a few so called -“sea-lilies.” They were animals with a central mouth surrounded by long, -jointed, flexible arms in multiples of five, and below this a small body -inclosed in calcareous plates, all at the top of a long jointed stem. -They lived in the sea and in the earlier geological times must have been -very abundant; for their remains are so common in places as to make -whole layers of limestone. - -Hydraulic Limestone is a fine-grained, compact, yellowish limestone with -from 13 to 17% of sand, and some clay; which, when it is burned at a -temperature a little higher than that used in burning lime, makes a -product, that, while not as strong as Portland cement, still like it -sets under water. - -Lithographic Limestone is a very fine-grained, compact limestone with -clay impurities, the finest of the grain making it usable for making the -stone plates used in lithographic printing. On slabs of this limestone -figures are drawn in reverse with a special crayon. Then the slab is -treated with acid, those parts which are not protected by the drawing -being etched away, while the points protected by the drawing remain in -low relief. From this slab figures can then be printed. - -Travertine is a general name, applied to calcareous deposits from fresh -water lakes or streams, and has been precipitated either as a result of -cooling or evaporation. Some travertines are porous, while others are -dense; some are white, while others are colored, often beautifully, by -impurities in the water. - -Porous deposits of travertine, when made on grass or other like -substances, are known as tufa or _calc sinter_. Such masses are common -around Caledonia, N. Y., Mammoth Hot Springs in the Yellowstone Park, -etc. - -Onyx marble is a dense travertine, usually formed as a result of the -deposition of lime from the water of springs. It is often banded, due to -the presence of impurities in the water at one time, and their absence -at other times. - - -Till - -Till is an unconsolidated mass of boulders, pebbles, sand and fine clay, -the unsorted material left behind by glaciers when they melted. The -boulders and pebbles, while they show some wear, are not rounded like -those that have been transported by streams, but have a more or less -angular shape; and some of them are polished or striated on one side, -where, while frozen in the ice, they were rubbed along the bottom. - -One of the most recent geological events in America was the extension of -the ice sheet, now covering Greenland, down over north and northeastern -North America, until it extended as far south as northern New Jersey, -the Ohio River and the Missouri River, and as far west as the Rocky -Mountains, but not over the Great Basin, the Cascade Ranges or Alaska. -This great mass of ice, thousands of feet thick, moved from two centers, -one either side of Hudson Bay, scraping up the loose soil, and grinding -off the exposed surfaces of the underlying rock. All this material it -carried southward, until the melting along its lower margin equaled the -rate at which it advanced. When the melting was faster than the advance -the glacial sheet retreated. At the southern limit of the advance this -débris was dropped, either making long ridges (moraines) or while the -ice was retreating, thicker or thinner sheets. This deposited débris is -till. - -The soil, and especially the subsoil, in all the regions formerly -covered by the ice sheet, is made up very largely of this till; which, -where it is undisturbed is often called “hardpan.” When till is mixed -with humus it becomes loam. This mixture of material, varying all the -way from the fine powdered products of the ice grinding to the great -boulder it picked up and carried south, is characteristic of this or any -other glaciated country. When this section of country was settled, the -boulders and stone were a hindrance to cultivation, and were picked up -and piled into stone walls, which are one of the first features to -strike the eye. - - -Tillite - -When till is consolidated into solid rock, it is known as tillite. In -several cases it has been found buried far beneath the more recent -sedimentary rocks; testifying that there were other glacial periods -beside the last one which furnished the till. - - - The Coal Series - -Disregarding minor constituents, the plants are largely made up of -cellulose, which is a combination of carbon, hydrogen, and oxygen, -(C₆H₁₀O₅). If this is heated in the air, where there is plenty of -oxygen, it disintegrates, or burns, making carbon dioxide and water; but -if the heating is done where the oxygen is excluded, as in a kiln, the -hydrogen and oxygen will be driven off and the carbon will remain behind -as charcoal. In Nature similar reactions go on, but more slowly. -Vegetable matter, exposed to the air, disintegrates into carbon dioxide -and water, and there is no solid residue. However, if the vegetable -matter is under water, which excludes the air more or less completely -including the oxygen in it, then disintegration still takes place, but -the products formed are water, (H₂O) marsh gas (CH₄), and some carbon -dioxide (CO₂), but a considerable part of the carbon remains behind and -accumulates. - -Thus in bogs, swamps and ponds, where dead vegetation, especially that -growing in the water, piles up, the oxidation is incomplete; so that -there gradually accumulates on the bottom a layer of brown to black mud, -known as _peat_. More plant remains are constantly being added, and the -layer may increase to several feet in thickness. The decomposition is -incomplete and some oxygen and hydrogen remain, but the carbon is in a -constantly increasing ratio and in proportion far above that in -cellulose. In the cold northern climates sphagnum moss is the most -efficient peat producing plant, but in temperate and tropical climates -the moss is replaced by the leaves, twigs, trunks, etc., of trees, -bushes, and vines. - -If these peat beds are buried beneath a layer or layers of sediment, -especially clay, the peat is sealed up and oxidation stops almost -entirely. With the pressure of the superincumbent beds, the peat becomes -more and more compact, and changes to a dark-brown or black color. It is -then known as _lignite_. If this lignite is buried still deeper, with -consequently more pressure and more time, it changes into the still -denser black _bituminous coal_. This is as far as it will go unless some -new agent is added to the forces already working. - -The next step in the series of changes forming coal is associated with -mountain making. In case the layers of rock containing beds of coal are -folded, and that presupposes at least a moderate increase in heat, the -bituminous coal is altered to _anthracite_, which is still denser, and -so hard that it breaks with a conchoidal fracture. Alteration may be -carried a step still farther, in case the rocks between which lie beds -of coal are effected by such high temperatures as accompany -metamorphism. Then all the associated hydrogen, oxygen and moisture are -driven off, and only the carbon remains, which is then known as -_graphite_. All steps between the stages especially designated occur. -The following represent steps only in the series of changes. - - -Peat - -Peat is a mass of unconsolidated vegetable matter, which has accumulated -under water, and in which the original plant remains are still, at least -in part, discernible. It contains a large amount of water, so that -before it can be used as a fuel, it is cut out in blocks, which are -piled up and left for a time to dry before using. It burns with a long -flame and considerable smoke. This country is so well supplied with -other fuels, that so far peat has been but little used. - - -Lignite -_brown coal_ - -Lignite is more compact than peat, and is found buried to some depth -under layers of clay or sandstone. It is dark brown to black in color, -and still retains pretty clear traces of the plants from which it was -derived. It also usually contains a considerable amount of moisture, and -when this is dried out, it tends to crumble badly, so that it is -undesirable to handle it much, or to ship it far, before using. It has a -fair fuel value and is fairly widely used; but it is very desirable that -some method be found, by which lignite could be treated to obtain its -by-products, and at the same time make it more compact, so it would not -crumble with the handling incident to using it in furnaces. There are -extensive lignite deposits in this country in North and South Dakota, -Montana, Wyoming, Colorado, New Mexico, Texas, Louisiana, and -Mississippi. - - -Bituminous Coal -_soft coal_ - -This type of coal is compact, black in color, and breaks readily, but -does not crumble as badly as lignite. It contains considerable water, -and still has some hydrogen and oxygen compounds in it. Bituminous coal -is the product of plant remains which have been preserved for long -periods, (millions of years), sealed from the air by the overlying beds -of rock. The pressure has made it compact, and nearly all traces of the -original plants have disappeared. - -Bituminous coal is our most abundant fuel, occurring the world over in -seams from less than an inch in thickness to some over fifteen feet -thick. The United States is peculiarly fortunate in the abundant and -easily accessible deposits of this type of coal, in Pennsylvania, West -Virginia, Ohio, Kentucky, Tennessee, Indiana, Illinois, Michigan, Iowa, -Missouri, Kansas, Nebraska, Texas, Utah, and Colorado. - -The volatile constituents, hydrogen and oxygen compounds, of bituminous -coal may be driven off by heating the coal in closed ovens, and the -residual mass is known as _coke_, almost pure carbon. This is -distillation, and the ovens in which this is done, without trying to -save the volatile products, are called bee-hive ovens, while the more -modern ovens which save the by-products are called by-products ovens. A -ton of bituminous coal treated in the typical by-products oven, will -yield on the average 1410 lb. of coke, 7.1 gallons of tar, 18.9 pounds -of ammonia sulphate, etc., 2.4 gallons of light oils, 10440 cubic feet -of illuminating gas, about half of this last being used to furnish the -heat for the distillation. The coal-tar dye industry is built on the tar -thus produced. Toluol, benzol, etc., come from the light oils; and half -the gas produced is available for household illumination, etc. Coke is -demanded, as it is a superior fuel for melting iron ores, iron and -steel, and is made regardless of whether the by-products are used. The -coke thus produced is hard, clean, and vesicular; but for some reason as -yet unknown, by no means all bituminous coal will produce a coke which -has this porous structure. These latter are known as “non-coking,” and -are of little use to the steel industry. - - -Cannel Coal - -This is a compact variety of non-coking bituminous coal, with a dull -luster and a conchoidal fracture. It contains the largest proportion of -volatile hydrocarbon compounds of any variety of coal; so that when the -supply of petroleum and natural gas gives out, this will be one of the -important sources of obtaining substitutes. Cannel coals occur in Ohio, -Indiana, and eastern Kentucky. This cannel coal owes its peculiar fatty -nature to the material from which it is derived, it being supposed to -have resulted from the accumulation of the spores of lycopod trees, and -their conversion to jelly-like masses by bacteria in the fresh-water -marshes of those ancient days. - - -Anthracite -_hard coal_ - -Anthracite coal is hard, black, has a luster, and breaks with a -conchoidal fracture. It contains but a low percentage of volatile -matter, and so burns with a short flame, and less smoke, than is the -case with the other coals. It is always associated with folded rocks, -and appears to have been formed as a result of the combined pressure and -the higher temperatures, which accompanied mountain making. Still the -temperature was not high enough to metamorphose the adjacent rocks. Most -of our anthracite comes from northeastern Pennsylvania. - - -Carbonite - -Carbonite is natural coke. It occurs in coal seams which have been cut -by dikes or intrusions of igneous rocks, the coal having been thus coked -by natural processes. It is not vesicular like artificial coke, for -which reason it is not useful as a fuel. Some carbonite is found in the -Cerillos coal field of New Mexico, in Colorado, and Virginia. - - -Jet - -Jet is a dense variety of lignite, a fossil wood of black color, which -takes a high polish and cuts easily into various ornamental shapes. It -has been used for ornaments since early ancient times, beads of jet -being found in the early bronze period in England, the supply probably -coming from the Yorkshire coast, whence the principal supply comes even -to the present day. In Switzerland and Belgium it was used still -earlier, even as far back as the Palæolithic age. Jet seems then to have -had a talismanic value, and to have been worn to protect the owner. -About 700 A.D. crosses and rosaries began to be made of jet, the custom -starting at Whitby Abbey, the material being obtained nearby, so that it -came to be known as “Whitby jet,” and in the eighteenth century became -very popular. In recent times it has been used mostly as jewelry -suitable for mourning. - - -Amber -Pl. 61 - -Amber is a gum which oozed from coniferous trees and was petrified. It -is associated with lignite beds of middle Tertiary age. It is usually -pale-yellow in color, but at times has a reddish or brownish tinge, and -is more or less transparent. It occurs in rounded irregular lumps, up to -ten pounds in weight, though most pieces are smaller; and is mostly -picked up along certain coasts where it is washed ashore by the waves. -Since the earliest records amber has been cast up on the shores of the -Baltic, and it was used by peoples as early as in the stone age for -ornaments and amulets. It has been found among the remains of the cave -dwellers of Switzerland, in Assyrian and Egyptian ruins of prehistoric -age, and in Mycenæ in the prehistoric graves of the Greeks, the first -recorded reference to it being in Homer, and the Greek name for amber -being _elektron_ from which our word electricity comes. All these finds -were of Baltic amber which was doubtless gathered and traded by those -early men. Even down to the present many men make their living, riding -along the shore at low tide and hunting for the amber washed ashore by -the waves. As early as 1860 the German geologists concluded that the -source of the amber must be lignite beds outcropping beneath the sea -level, and started mining for the amber with fair success, so that today -two types of Baltic amber are distinguished, “sea stone” which is washed -ashore, and “mine stone” taken from the mines. Beside the Baltic -locality, it is found along the shores of the Adriatic, Sicily, France, -China, and occasionally of North America. - -Some pieces of amber are found with insects inclosed and preserved -almost as perfectly as if collected yesterday. They were apparently -entangled in the gum while still viscid and completely embedded, before -fossilization. - - - The Petroleum Series - -Certain sedimentary rocks contain larger or smaller quantities of -natural gas, petroleum, mineral tar and asphalt. These are compounds of -carbon and hydrogen, or hydrocarbons, and range from gases to solids, -each being a mixture of two or more hydrocarbon compounds. The crude -petroleum may have either a paraffin base or an asphalt base: in the -former case, when the gas, gasoline, kerosene, etc., have been removed -by distillation, the solid residue will be paraffin, as in most of the -Pennsylvania crude oils; while in the latter case, the solid residue -will be an asphalt, as in most of the California and Texas crude oils. -In the case of the paraffin series all the compounds belong to the -paraffin group, while the asphalt is due to the presence, in addition to -the paraffin group, of some of the benzine series of hydrocarbons. - -Petroleum is found in sands and shales, which were originally deposited -on ancient sea bottoms, the shales generally being the real source of -the petroleum. The oil was once the fatty portion of animal bodies -(perhaps to some extent of plant bodies), and was separated during -decomposition as a result of bacterial activity. Oil thus produced is in -tiny droplets, which have a great affinity for clay. After being freed -by the bacteria, the oil droplets in muddy water attach themselves to -particles of clay, and as the clay settles the oil is carried down with -it, the two eventually making a bituminous shale. In clear water, or in -water which is in motion, the oil droplets rise to the surface and -eventually distill into the air. - -The oil, or petroleum, may stay diffused through the shales, in which -case we have _oil-bearing shales_, with sometimes as much as 20% of oil. -Were there but ¹/₁₀₀₀ of a per cent of oil in a layer of shale 1500 feet -thick, this would amount to 750,000 barrels per square mile which is -equal to a rich production from wells. When the oil in shale amounts to -three per cent or more, it is commercially usable. There are large -stretches of petroleum-bearing rocks in New York, Pennsylvania, Ohio, -Indiana, and all the way out to the Pacific coast, some of them with oil -so abundant, that a blow of the hammer will cause them to smell of -petroleum. - -In case these oil-bearing shales have been heavily overburdened and -compressed, the petroleum may have been more or less completely pressed -out of them. Then the droplets uniting have formed a liquid, which has -moved out from the shale, and gone wherever it could find open spaces. -Sandstones have frequently offered their pore space, and as it filled, -have been thus saturated with petroleum. If the sandstones were open to -the air, or if fissures extended from them to the surface, the oil has -escaped to the surface and evaporated into the air. But in those cases -where the sandstone (or other permeable rocks) was covered by an -impervious layer, like a dense shale or clay, the oil was confined below -the covering layer of rock. Crude oil is lighter than water; so that -when natural gas, petroleum and water were all present in the rocks, the -gas lies on top, the petroleum next, and the water underneath. With this -in mind it is easy to see, that in slightly folded or undulating layers -of rock, the gas and petroleum would be caught under upraised folds and -domes. This is the basis of prospecting for oil. - -If petroleum-bearing layers are depressed far enough beneath the surface -to be affected by the high temperatures of the earth’s interior, or have -been near volcanic activity, of course the petroleum has been distilled -by natural processes, and at most only the residues, like paraffin or -asphalt, have remained. For this reason it is impossible to find -petroleum in igneous or metamorphic rocks. - - -Natural gas - -Natural gas is the lightest portion of crude oil, and consists mostly of -marsh gas (“fire damp,” CH₄) together with other light hydrocarbons, -like ethane (C₂H₆), ethylene (C₂H₄), and some carbon dioxide and -monoxide. It is colorless, odorless, and burns with a luminous flame. -Mixed with air it is explosive. It is found in sedimentary rocks, mostly -sandstones, either with or without petroleum. Usually it is under -considerable pressure, and escapes with great force wherever a hole -permits. In time the gas all escapes through the hole or well, and then -the well “runs out.” If petroleum is present under the natural gas, the -hole may become an “oil well,” from which petroleum may be pumped, until -it in turn is exhausted. The end of an oil supply is usually indicated -by the appearance of water in the well. Natural gas is mostly associated -with oil districts, as in Pennsylvania, Ohio, Illinois, Texas, -California, etc. - - -Petroleum Crude Oil -Pl. 61 - -Petroleum is a mixture of paraffin compounds all the way from the gases, -through gasoline, kerosene, lubricating oils, and vasoline to paraffin. -In some of the crude oils there is also an admixture of compounds from -the benzine series, in which case, when all the volatile compounds have -been distilled off, an asphalt remains. The different components of -petroleum may be separated out by heating the crude oil in closed tanks, -and drawing off the various substances at the proper temperatures. - -Petroleum occurs in sedimentary rocks of marine origin, usually rocks -which also contain the shells of some of the animals, the soft parts of -which made the oil. To have been preserved the millions of years since -the petroleum was first formed, the oil-bearing layers must have been -covered by some impervious layer of rock, beneath the domes and -anticlines of which the oil has lain ever since. When such a dome or -anticlinal fold is perforated by a well, the released oil flows to the -surface with a greater or less rush, according to the pressure. Wells -may keep flowing for 20 years, sometimes more, sometimes much less. -Those which flow with the greatest pressure usually are relatively short -lived, at times lasting only a year or two. When this easily obtained -oil is exhausted, there is an even greater supply to be obtained by the -distillation of the bituminous shales. Petroleum never occurs in igneous -or metamorphic rocks, but is found in either sandstones or shales, in -places favorable for accumulation, all across that great stretch of -ancient sea bottoms, extending from the Appalachian Mountains to the -Rocky Mountains, and in the Great Basin between the Rocky Mountains and -the Sierra Nevada Range, and also to the west of the Sierras. - - -Bitumen - -Where petroleum has escaped through pores in the rocks, or by way of -fissures, and has come to the surface of the earth, the lighter -components, thus exposed to the air, have vaporized and escaped, leaving -behind a more or less solid residue, which is known as bitumen. If the -escape was through a fissure, the bitumen may have accumulated in the -fissure until it was filled, making vein bitumen. Or the escape may have -been so rapid that the petroleum formed a pool or lake from the surface -of which evaporation took place. In time such a pool will give off the -gases and volatile compounds, only a residue remaining to make a pitch -lake, like the one at Rancho Le Brea near Los Angeles, or an asphalt -lake like the one on the island of Trinidad. On account of their varying -hardness and composition, some of these bitumens have received special -names; as: - -Albertite, a black bitumen with a brilliant luster on broken surfaces, a -hardness between 1 and 2, and a specific gravity a shade over 1. - -Grahamite, a black bitumen, which is brittle, but has a dull luster, a -hardness of 2, and a specific gravity of 1.15. - -Gilsonite or Uintaite, a black bitumen with a brilliant luster and a -conchoidal fracture, a hardness of 2 to 2½, and a specific gravity of -1.06. - -Malta is a semi-liquid viscid natural bitumen, which has a considerable -distribution in California. - -The above varieties of bitumen look a good deal like coal, but are -easily distinguished by their lightness (weight about half that of -coal), and the fact that with only moderate heat they melt, and become a -thick liquid like tar. - - -Guano - -Guano is the accumulation of the excrement of birds (or of other animals -like bats) on areas so dry that, though soluble, it is not leached and -washed away. It may also contain some of the bones and mummified -carcasses of the birds which died on the spot. The greatest of these -deposits are on several small islands, just off the west coast of Peru, -and now “farmed” by the Peruvian government. In this country there are -no true guano beds, except a few accumulations of bat guano in certain -caves of Kentucky and Texas, but these are not large enough to become of -commercial importance. - - -Phosphate Rock - -Phosphate rock is one composed chiefly of calcium phosphate along with -various impurities, such as clay and lime. It occurs in beds, irregular -masses, or as concretionary nodules in limestone or sand. - -The bedded varieties are in the older sedimentary rocks, in which the -phosphate runs from a small percentage up to as high as 85%. Ultimately -the phosphate came from either animal excrement, or from bacterial -decomposition of animal carcasses and bones. In all the beds it seems to -be true that in the first instance the phosphate was laid down as a -disseminated deposit in marine beds, usually limestones. Later by the -action of water leaching through the rocks, the phosphate was dissolved, -and then redeposited elsewhere in a more concentrated form. This may be -either in the underlying sandstones, but is more often in limestones, -replacing the original lime. - -In these secondary deposits, if the phosphate has been laid down in -cavities, the resulting phosphate will be in nodular masses. In the case -of the Florida and Carolina deposits, these nodules have been freed from -their matrix and washed along the river beds, remaining as pebbles in -the river sands. The bed deposits are mostly in Kentucky and Idaho. The -commercial use for such phosphate rocks is of course the making of -fertilizers. - - -Diatomaceous Earth -Pl. 62 - -Diatoms are tiny single-celled plants living in uncounted millions in -the fresh and salt water. Each diatom builds around itself two shells -which fit into each other like the cover and box of a pill-box, and each -shell is marvelously ornamented. The shells are composed of silica of -the opal type. In size the diatoms range from ¹/₅₀₀₀ of an inch in -diameter up to the size of a pin head, and they live in such numbers -that ordinary surface waters have hundreds of them to the quart, and -where they are flourishing up to 250,000 in a quart. When the plants -die, or in order to reproduce abandon the shells, these shells fall to -the bottom of the pond or the sea, and there accumulate, often making a -layer from a few inches thick up to hundreds of feet in extreme cases. -If unconsolidated, this mass of tiny shells is known as diatomaceous -earth; but if they are consolidated it is called tripolite, so named -because the first of them used commercially came from Tripoli. - -As the shells are tiny and uniform in size and have a hardness of 6, the -diatomaceous earth is used to make a great variety of polishes, scouring -soaps, tooth paste, as a filler in certain kinds of paper, in making -waterglass, as an absorbent for nitroglycerine, and as packing in -insulating compounds, where asbestos would otherwise be used. - -Deposits of freshwater diatoms are found all over the United States, -usually in thin layers of limited extent, especially in Massachusetts, -New York, Michigan, etc. The marine deposits of diatoms are on a much -larger scale, there being beds of diatoms in Anne Arundel, Calvert and -Charles Counties, Md., up to 25 or 30 feet in thickness. In Santa -Barbara County, Cal., there is one bed 2400 feet thick and another 4700 -feet thick, beside many other smaller ones. The enormous former wealth -of life indicated by these great deposits may be suggested, when it is -remembered that it takes about 120,000,000 to make an ounce in weight. -They reproduce on an average about once in five days, so that from a -single diatom the offspring possible under favorable conditions would -amount to over 16,000,000 in four months or over 60 tons in a year. Of -such an order is the potential increase of animals or plants, no matter -how small, if the rate of reproduction is high. - - - Metamorphic Rocks - -Either a sedimentary or an igneous rock, which has been altered by the -combined activities of heat, pressure and chemical action, becomes a -metamorphic rock. The process is essentially one, during which the -layers of rock come under the influence of such temperatures as are -associated with the formation of granite or lavas. Such material as is -actually melted becomes igneous rock, but adjacent to the masses -actually melted are other rocks which do not melt but, according to the -temperature, are more or less changed, and these are the metamorphic -rocks. At a distance from the molten masses the changes are minor, but -close to the molten magmas extensive changes take place. Though not -actually melted the rock near the heat center may be softened, usually -is, in which case pebbles and grains or even crystals become soft and -plastic, and, as a result of the great pressure, are flattened, giving -the rock, when it cools again, a striated appearance. At these high -temperatures the water in the rock and also some other substances -vaporize, and the hot steam and vapor are active agents in making a -great many chemical changes. In some cases material like clay is changed -into micas, or chlorite, etc.; in other cases the elements of a mineral -will be segregated and large crystals will appear scattered through the -metamorphic rock, such as garnets, staurolites, etc. - -If one studies a layer of rock both near and far from the molten mass, -all grades of change will appear. For example, at a distance a -conglomerate maybe unaltered; somewhat nearer the molten mass, the heat -and steam may have softened (but not melted) the pebbles and then the -pressure has flattened them as though they were dough; and nearest the -molten mass, the outlines of the pebbles are lost, only a layered effect -remaining, and many of the materials have changed into new minerals, -like mica, garnets, etc., but still the layered effect is preserved. - -One of the effects of heat and pressure is to flatten the component -particles of the rock, so that it tends to split in a direction at right -angles to the direction of the pressure, just as particles of flour are -softened and flattened under the pressure of the roller; and then when -the crust is baked it splits or cleaves at right angles to the direction -in which the pressure was exerted by the roller. This tendency to split -is not to be confused with either the layering, characteristic of -sedimentary rocks, nor the cleavage characteristic of minerals. It has -nothing to do with the way the particles were originally deposited, nor -with their cleavage; but is due to the pressure, and resembles the pie -crust splitting, being irregular and flaky. This is designated -_schistosity_ if irregular and _slaty cleavage_ if regular. Schistosity -refers to the flaky manner of splitting into thin scales as in mica -schists. Slaty cleavage is more regular, this being due to the fact that -the material of which slate is made is small particles of clay of -uniform size. - -The metamorphic rocks are generally more or less folded, as they are -always associated with mountain making. These major folds are of large -size, from a hundred feet across to several miles from one side to the -other. Such folds may also occur in sedimentary rocks or even in igneous -rocks and simply express the great lines of yielding, or movement of the -crust of the earth. In addition to this there is minor folding or -contorting which is characteristic of metamorphic rocks only. When the -rocks were heated by their nearness to the molten igneous magmas, they -must expand, but being overburdened by thick layers of other rocks, -there is no opportunity for yielding vertically, so the layers crumple, -making minor folds from a fraction of an inch to a few feet across. Such -crumpling, which is so very conspicuous especially where there are bands -of quartzite in the rock, is entirely characteristic of metamorphic -rocks. It is seen on hosts of the rocks about New York City, all over -New England, and in any other metamorphic region. Plate 63 is a -photograph of such a crumpled rock which has been smoothed by the -glacial ice. - -The metamorphic rocks are the most difficult of all the rocks to -determine and understand, because the amount of change through which -they have gone is greatest, but for this same reason they offer the most -interest, for the agents which caused the changes are of the most -dramatic type of any that occur in Nature. From one place to another a -single layer of metamorphic rock changes according to the greater or -less heat to which it was subjected, making a series of related rocks of -the same composition but with varied amount of alteration. For this -reason in naming metamorphic rocks, a type is named, and from that there -will be gradations in one or more directions, both according to -composition, and according to amount of heat involved. If it is possible -to follow a given layer of metamorphic rock from one place to another -this is of great interest; for by this means, many variations in the -type will be found, both those resulting from a different amount of -heat, and those due to the local changes in the composition of the -original rock. - -One further consideration has to be kept in mind. When a rock is -metamorphosed the high temperatures either drive off all water, or the -water may be used up in the making of some of the complex minerals. When -such a metamorphic rock later comes near the surface and is exposed to -the presence of ground water, and that leaching down from the surface -into the rocks, several of the minerals formed at high temperatures will -take up this water and make new minerals such as serpentine, chlorite, -etc. They are always associated with metamorphic rocks, and have been -metamorphic rocks, but since then have become hydrated, forming minerals -not at all characteristic of high temperature. - -The following shows the relation of the sedimentary and igneous rocks to -their metamorphic equivalents. - - _Loose sediment_ _Consolidated sediment_ _Metamorphic - equivalent_ - - gravel conglomerate gneiss - sand (quartz) sandstone quartzite - mud (sand and clay) shale schist - clay shale slate or phyllite - marl limestone marble - peat bituminous coal anthracite to - graphite - coarse igneous rocks such as gneiss - granite, syenite, etc. - fine igneous rocks such as schist - trachite, rhyolite, etc. - -In working out the past history of any given region, much of it is done -on the basis of this series of equivalents. The finding of limestone, -for instance, indicates that the given area was at one time under the -sea to a considerable depth, that is from 100 to 1000 feet, but not -ocean-bottom depths which run in tens of thousands of feet. Marble -indicates the same thing, and so one can go on through all these types -of rock. - - -Gneiss -Pl. 64 - -Gneiss is an old word used by the Saxon miners, and is often very -loosely used. Here it is used in its structural sense, and a gneiss may -be defined as: a banded metamorphic rock, derived either from a -sedimentary or an igneous rock, and is composed of feldspar, quartz, and -mica or hornblende, and is coarse enough, so that the constituent -minerals can be determined by the eye. It corresponds to a granite, or -some sedimentary rock like gravel or conglomerate. - -Due to the action of pressure, all the gneisses are banded, and the -original constituent particles or crystals are distorted. The lines of -banding may be long or short, straight, curved or contorted. When the -banding is not conspicuous, the gneiss tends toward a granite. When the -banding is thin and the structure appears flaky, the gneiss tends toward -a schist. The color varies according to the constituent minerals, from -nearly white, through red, gray, brown, or green to nearly black. Plate -64 shows one gneiss which is in a less advanced stage, the pebbles being -simply flattened and the matrix partly altered to micaceous minerals, -and a second gneiss which is so far advanced that the original -constituents are all altered to other minerals and only the banded -structure remains. This latter type would have required but little more -heat to have completed the melting and changed this to a granite. - -Gneisses are very compact and have little or no pore space in them. They -are hard and strong and resist weathering well, so that they are widely -used as building stone: but they are not as good as granite for this -purpose, as they split more readily in one direction and can not -therefore be worked so uniformly as can granite. - -There are many varieties of gneiss, based either on their origin, -composition, or their structure, as follows: - - Granite-gneiss is one derived by metamorphism from granite. - Syenite-gneiss is one derived by metamorphism from syenite. - Diorite-gneiss is one derived by metamorphism from diorite. - Gabbro-gneiss is one derived by metamorphism from gabbro. - Biotite-gneiss is one composed of quartz, feldspar and biotite. - Muscovite-gneiss is one composed of quartz, feldspar and muscovite. - Hornblende-gneiss is one composed of quartz, feldspar and hornblende. - Banded-gneiss is one in which the banded structure shows clearly. - Foliated-gneiss is one in which there is thin irregular layering. - Augen-gneiss is one which has concretionary lumps scattered through - it. - -Gneisses have a wide distribution over all New England, most of Canada, -the Piedmont Plateau, the Lake Superior region, the Rocky Mountains, the -Sierra Nevada and the Cascade Ranges. - - -Quartzite - -Quartzite is metamorphosed sand or sandstone, and frequently grades into -one or the other. It is a hard compact crystalline rock, which breaks -with a splintery or conchoidal fracture. It is distinguished from -sandstone by the almost complete lack of pore spaces, its greater -hardness and by its crystalline structure. In practice it may be -distinguished by the fact that a sandstone in breaking separates between -the grains of sand, while a quartzite breaks through the grains. - -Some quartzites are almost pure quartz, but others contain impurities of -clay, lime or iron, which were in the original sandstone. These alter in -the metamorphism to such accessory minerals as feldspar, mica, cyanite, -magnetite, hematite, calcite, graphite, etc. The color of quartzite when -pure is white, but may be altered to red, yellow, or green by the -presence of these accessory minerals. - -On account of the difficulty of working the quartzites, they are not -much used in building, though they are very durable. When crushed they -often make excellent road ballast, or filling for concrete work. The -pure varieties are sometimes ground and used in the manufacture of -glass. - -According to the accessory mineral, the following varieties may be -distinguished; chloritic-quartzite, micaceous-quartzite, -feldspathic-quartzite, etc. - -Quartzites are common in the New England, the Piedmont Plateau, and Lake -Superior metamorphic regions, and also in many western localities. - - -Schist -Pl. 65 - -Schist is a loosely used term, but is used here in its structural sense. -It includes those metamorphic rocks which are foliated or composed of -thin scaly layers, all more or less alike. The principle minerals are -recognizable with the naked eye. In general schists lack feldspar, but -there are some special cases in which it may be present. Quartz is an -abundant component of schists; and with it there will be one or more -minerals of the following groups: mica, chlorite, talc, amphibole or -pyroxene. Frequently there are also accessory minerals present, like -garnet, staurolite, tourmaline, pyrite, magnetite, etc. - -All schists have the schistose structure, and split in one direction -with a more or less smooth, though often irregular, surface. At right -angles to this surface they break with greater or less difficulty and -with a frayed edge. As they get coarser, the schists may grade into -gneisses, losing their scaly structure: while on the other side, as the -constituent minerals become finer and so small as to be difficult of -recognition, schists may grade into slates. - -The varieties of schist are based on the mineral associated with the -quartz; as mica-schist, chlorite-schist, hornblende-schist, talc-schist, -etc. - -The color also is due to the constituent minerals other than quartz and -ranges widely, mica-schists being white to brown or nearly black, -chlorite-schists some shade of green, hornblende-schists from dark green -to black, talc-schists white, pale-green, yellowish or gray, etc. - -Schists are found all over the same regions as gneisses and quartzites, -_i.e._, New England (especially good exposures of schist being seen -about New York City), the Lake Superior region, Rocky Mountains, etc. -Beside these regions where it occurs native, there are boulders of -schist all over the glaciated areas of eastern and northern United -States. - - -Slate - -Slate is a metamorphic rock which will split into thin or thick sheets, -and is composed of grains so fine as to be indistinguishable to the -unaided eye. The cleavage is the result of pressure during metamorphism, -and has nothing to do with the bedding or stratification of the -sedimentary rock from which it was derived. The original bedding planes -may appear as streaks, often more or less plicated, and running at any -angle with the cleavage. If these bedding streaks are abundant or very -marked, they may make a slate unsuitable for commercial uses. The slaty -cleavage may be very perfect and smooth so that the rock splits into -fine sheets, in which case it is often used for roofing slate; but by -far the greater part of the slates have a cleavage which is not smooth -or perfect enough so that they can be so used. Slates are the -metamorphic equivalents of shales and muds, and represent the effect of -great pressure but with less heat than is associated with schists or -phyllite, and consequently with less alteration of the original mineral -grains. - -The color ranges from gray through red, green and purple to black. The -grays and black are due to the presence of more or less carbonaceous -material in the original rock, the carbon compounds having changed to -graphite. The reds and purple are due to the presence of iron oxides, -and the green to the presence of chlorite. - -While the particles of slate are so small as to be indistinguishable to -the unaided eye, the use of thin sections under the microscope shows -that slate is composed mostly of quartz and mica, with a wide range of -accessory minerals, like chlorite, feldspar, magnetite, hematite, -pyrite, calcite, graphite, etc. - -According to their chief constituents slates may be distinguished as -argillaceous-slate or _argillite_, bituminous-slate, calcareous-slate, -siliceous-slate, etc. - -Slate will be found here and there in the metamorphic areas of New -England, the Piedmont Plateau, the Lake Superior region, and in many -places in the west. - - -Phyllite -Pl. 66 - -Phyllite is a thinly cleavable, finely micaceous rock of uniform -composition, which is intermediate between slate and mica schist. In -this case the flakes of mica are large enough to be distinguishable to -the eye, but most of the rest of the material can only be identified -with the aid of a microscope. It is mostly quartz and sericite. Phyllite -represents a degree of metamorphism greater than for slate, but less -than for schist; and it may grade into either of these other rocks. -Garnets, pyrite, etc., may be present as accessory minerals. The color -ranges from nearly white to black, and it is likely to occur in the same -places as do slates. - - -Marble -Pl. 66 - -This is a broad term, and includes all those rocks composed essentially -of calcium carbonate (limestones) or its mixture with magnesium -carbonate (dolomite), which are crystalline, or of granular structure, -as a result of metamorphism. It takes less heat to metamorphose a -limestone, and for this reason the marbles have a more crystalline -structure than most metamorphic rocks; and they do not have the tendency -to split or cleave which is so characteristic of most metamorphic rocks. -It is only when there is a large amount of mica present that the typical -schistosity appears. Commercially the term marble is used to include -true marble and also those limestones which will take a high polish; but -in this book, and geologically speaking, no rock is a marble unless it -has crystalline structure. - -Marbles range widely in color according to their impurities. Pure marble -is white. Carbonaceous material in the antecedent limestone is changed -to graphite in the metamorphic process, and makes the marble black, but -appears usually in streaks or spots, rather than in any uniform color. -An all black “marble” is usually a limestone. The presence of iron -colors the marble red or pink. Chlorite makes it green, etc. - -Various accessory minerals are common in marbles, such as mica, -pyroxene, amphibole, grossularite among the garnets, magnetite, spinel, -pyrite, etc., through a long list. - -Because it cuts readily in all directions and takes a high polish, -marble is widely used as a building stone. In the moist climate of the -United States it suffers in being soluble in rain water when used on the -outside of a building: but for interior decoration it furnishes some of -the finest effects. - -The largest marble quarries are developed in Vermont, Massachusetts, New -York, Pennsylvania, Georgia, Alabama, Colorado, California, and -Washington. - - -Steatite -_Soapstone_ - -Steatite is a rock composed essentially of talc, which is associated -with more or less impurities, such as mica, tremolite, enstatite, -quartz, magnetite, etc. It is found in and with metamorphic rocks, and -is a rock which has been modified by hydration from a metamorphic -predecessor. It was probably first a tremolite or enstatite schist, in -which, after the metamorphic rock came into the zone where ground water -exists, the tremolite or enstatite was altered to talc, the impurities -remaining much as they were in the first place. - -It is bluish-gray to green in color, often soft enough to cut with a -knife, and has a greasy feel. It is very resistant to heat and acids; -for which reasons it has proved very useful commercially in making -hearthstones, laundry tubs, and fire backs; and, when powdered, in -making certain lubricants. The Indians, in the days before Columbus, -took advantage of the ease with which it is cut, to make from it large -pots for holding liquids, which are today among the greatest treasures -in collections of Indian relics. They also carved pipe-bowls and various -ornaments and amulets from soapstone. - -It is found in Vermont, Massachusetts, New York, New Jersey, -Pennsylvania, Maryland, Virginia, North Carolina, Georgia and -California. - - -Serpentine -Pl. 67 - -Pure serpentine is the hydrated silicate of magnesium, as described -among the minerals on page 138. Serpentine rock is serpentine with more -or less impurities, such as pyroxene, amphibole, olivine, magnetite, -chromite, calcite, magnesite, etc. It often also contains mica and such -garnets as pyrope, as accessory minerals. Serpentine, like steatite, -always occurs in and with metamorphic rocks, and was originally a -metamorphic rock, but has since been changed by the hydration of its -silicates, when it came into the zone in which ground water is present. -In the first instance it was some sort of shale, clay and dolomite, -which was metamorphosed to an amphibole or pyroxene schist. When this -was exposed to the action of ground water, the amphibole or pyroxene -minerals were changed to serpentine, resulting in a rock composed mostly -of serpentine, but retaining the impurities which were in the -metamorphic rock, and perhaps adding to them such amphiboles and -pyroxenes as were not altered during the hydration process. The above is -the commonest type of serpentine rock. It can and sometimes has been -formed in a similar way from an igneous predecessor, by the hydration of -its silicate minerals. In this latter case the serpentine would not be a -modified metamorphic rock, but a modified igneous one. It is a case -where such a rock as a diorite or a gabbro is exposed to ground water -and the pyroxene present altered to serpentine. A serpentine formed in -this way would be a very impure one. - -Serpentine rock is used as an ornamental stone for interior decoration, -because it takes a high polish and has pleasing colors, various shades -of green. It is however decidedly soft and will stand very little -exposure to weather, and it is also filled with seams which make it -difficult to get out large slabs. - -Serpentine rock occurs fairly commonly in the metamorphic belt of New -England and the Piedmont Plateau, and in some of the western states, -especially California, Oregon, and Washington. - - -Ophiolite -_Ophicalcite_ - -This name is given to marbles which are streaked and spotted with -serpentine. They are a mixture of green serpentine and a white or nearly -white calcite, magnesite or dolomite in variable proportions. - -Ophicalcite occurs in and with metamorphic rocks, and represents an -impure limestone which has been metamorphised, the lime becoming marble, -and the impurities becoming such silicates as pyroxene, amphibole, or -olivine. This metamorphic rock has then come into the zone of -ground-water and the silicate minerals have been changed by hydration to -serpentine. Ophicalcite is then a metamorphic rock, in which secondary -chemical changes have since taken place. It may have a wide range of -accessory minerals present, such as magnetite, chromite, pyrope among -the garnets, olivine, etc. Verde antique is a trade name for one of the -ophiolites. - -While not abundant, ophicalcite is in good demand as an ornamental stone -for interior work; for it takes a high polish, and is beautiful; but, on -the other hand, it will not stand exposure to the weather for the -calcite is soluble, and there are numerous seams and cracks in it making -it difficult to obtain large slabs. - -It occurs in Quebec, Canada, in the Green Mountains of Vermont, and in -the Adirondack Mountains. - - - - - CHAPTER V - MISCELLANEOUS ROCKS - - -There are a few rocks which do not fit into any of the three groups -described, such as concretions, geodes, meteorites, etc., and they are -gathered together here. There is also one type of rock, which really -belongs among the minerals, but is likely not to be so recognized at -first glance, and that is the material filling veins. These last are -sometimes designated “vein rocks,” but are really massive deposits of -one, two or more minerals, and should be referred to the minerals when -found. - - - Concretions - -In the sedimentary rocks there frequently occur inclusions of a nature -different from the surrounding rock. In shape they are usually rounded, -nodular, spherical, discoidal, ovate, flattened, elongated or -ring-shaped, or combinations of the foregoing, making often curious and -fantastic forms. In size they range from a fraction of an inch in -diameter to several feet through. When broken, they may show a nucleus, -around which more or less concentric layers have formed, or neither -nucleus nor concentric structure may be visible. The layered structure -of the surrounding rock in some cases continues right through the -nodular mass. These structures are called concretions, and their -formation in all cases is at least due to similar reactions. - -In general the concretions differ from the surrounding rock in -composition, but are usually composed of some one of its impurities, of -lime in the clays or silica in limestones, of iron oxide in sandstone, -etc. They seem to have originated as a result of the solution of the -minor mineral, and then its redeposition around some center or nucleus. -In many cases the nucleus is organic, such as a leaf, a shell, a bone, -etc., so that when the concretion is split, in its center will be found -the perfect imprint of the leaf, or the shell of a mollusk, or a bone of -a higher animal, sometimes a whole skeleton. Again the nucleus may be -inorganic like a grain of sand; and in still other cases no nucleus can -be found, though there was probably one in the beginning. What has -happened is somewhat like the case of accessory minerals in igneous and -metamorphic rocks. A layer of sediment was laid down, including in it, -here and there, something foreign to the run of the rock. Later when the -water leaches through this rock, impregnated with lime for instance, it -comes to the point where a leaf is decomposing. The products of the leaf -decomposition are different from what is already present in solution, -and may precipitate some of the lime in that neighborhood. As long as -leaf decomposition continues the precipitation in that region will -continue and increase the size of the concretion. This sort of action -accounts for many of the concretions, especially those about organic -remains. In some other cases where there is no nucleus, as the flint in -chalk, what has taken place is that the small amounts of silica in the -lime have been dissolved, and then around some center has constantly -been added more and more non-crystalline silica until a mass of flint -has accumulated. There may be a considerable variety of ways to account -for different concretions, but in all cases solutions of one mineral -have come in contact with solutions of a different kind, and -precipitation about a center has resulted. - - -Clay stones -Pl. 68 - -Of all the concretions these are perhaps the commonest, being found in -the clays of all types and in many regions. They are made of lime and -precipitated around some nucleus of foreign matter. The shapes vary -widely, usually discs, flattened ovals or even rings, in most all cases -however flattened. This is indicative of the water moving though the -clay more freely in some layers than others. Often clay stones occur so -abundantly that two or more have grown together making fantastic shapes, -sometimes resembling animals, and all sorts of fancied but unrelated -objects. As the clay stones have grown the clay has not been pushed -aside, but has been incorporated within the concretion; so that when a -concretion is dissolved in acid, it yields not only the lime, which is -its reason for being, but also a large amount of clay. - -Claystones are found in clays most anywhere, usually occurring in -certain layers and being absent from others. - - -Lime concretions - -These are found mostly in shales which carry a high percentage of clay -as impurities, and are characteristic of the older geological -formations, especially ancient sea bottoms. They are likely to have as a -nucleus some shell, fish bone, or a leaf, which when the concretion is -split, reveals a wonderfully preserved portion of an animal or a plant, -which was buried millions of years ago. The lime concretion is closely -related to the claystone, and is really a claystone which has been -buried so long that the surrounding matrix has changed to a shale -instead of remaining clay. - -One of the most famous localities for these lime concretions is Mazon -Creek, Illinois, where thousands of these concretions have been picked -up and split to study the organic remains included. The commonest -objects found are fern leaves, like the one on Plate 68. But about once -in a thousand times they inclose a spider or insect, and once in ten -thousand times the skeleton of an amphibian, which is of especial -interest, as here have been thus found the remains of the very earliest -of the land animals. These remains were inclosed in these concretions -during the coal age, probably 50,000,000 years ago, and once inclosed -all the hard parts have been as well preserved after that long interval, -as they were immediately after being inclosed in the concretion. Lime -concretions range from less than an inch in diameter to several feet -through. They are not confined to shales, but sometimes occur in -sandstones, in this case also usually having as a nucleus either a -shell, or the bone, or bones, of some animal. - -They are likely to be found anywhere in the limestone belt, from the -Appalachian Mountains to the Rocky Mountains, or in the Great Basin, or -on the Pacific Coast. Often they have been mistaken for turtles and -other objects. A good many of the cases where the head or body of -animals “petrified with all the flesh” are reported, it is one of these -concretions which has a shape sufficiently like the part described, for -the imagination to construct the rest. - - -Septeria -Pl. 69 - -Septeria are lime concretions, which, after they had formed, have shrunk -and developed a series of cracks running through them in all sorts of -directions, and since then the cracks have been filled with various -minerals, such as calcite, dolomite, and siderite. These make a series -of veins which intersect the concretion, in a sort of network. Septeria -are mostly of considerable size, ranging from six inches in diameter to -several feet through. They are characteristic of the shales of ancient -sea bottoms, especially those of Devonian age in New York, and -Pennsylvania, and those of Cretaceous age in Wyoming, Montana and the -Dakotas. - - -Flint concretions - -The silica in limestones is often segregated into nodular masses of -varying sizes, to make concretions of flint. Such masses have grown in -the limestone, and, while growing, have either pushed away, or dissolved -the adjacent limestone, so that the flint nodule is pure silica. They -are especially characteristic of the chalk beds, and of ancient -limestones which formed on the floor of the sea, like the Helderberg -Limestone of New York, Pennsylvania, Ohio, etc. When thin sections are -cut through these flints, and examined under the microscope, many -remnants of the shells of plants and animals are still recognizable. A -nucleus is seldom found, but in some cases there is a fossil in the -nodule about which the concretion doubtless formed. The spicules of -sponges, shells of diatoms, and of radiolarians seem to have contributed -most of the material from which flint concretions are formed. In -addition to the silica there are frequently inclosed in these nodules -the horny jaws of various sea worms, and a host of spiny balls the -relationships of which are still unknown. - - -Sandstone concretions - -There are two types of sandstone concretions, first those which are -cemented with lime, and second those cemented with iron oxide. The -concretions bound by lime are especially characteristic of sandstones -which were laid down as river deposits, either in the channels or on the -flood plains, and also the sandy deposits resulting from wind -deposition. In these cases the concretions will mostly be found to have -formed around some organic nucleus, most frequently about a bone, or -group of bones, of some ancient animal. In this country they are mostly -found in the arid and semiarid sections of the West, where the present -day wind erosion exposes the harder parts of bluffs, etc. - -The second type of sandstone concretion is the one in which the cement -is most often limonite, less often hematite. These concretions are less -dense than the lime ones, and in some cases the limonite is only -precipitated at a distance from the nucleus, which has resulted in the -formation of a hollow shell, filled with loose sand. This is especially -characteristic of certain concretions, found in a gravel or coarse sand -in the region of Middletown, Del. - - -Oolites - -In large bodies of water like the sea and some larger lakes we find -concretions which have formed, or are still forming, about tiny grains -of sand, which are still being moved about by the waves and currents. In -such cases not only are great masses of concretions formed but they have -very clearly marked the concentric layering, which shows that they have -increased in size, sometimes more rapidly and sometimes more slowly. -Where great masses of such concretions have formed the resulting rock -appears like a great mass of small eggs, whence the term oolite. The -cement may be any one of several substances, but lime, silica, and -hematite are perhaps the most common. Here and there are found larger or -smaller masses of this oolite. In some cases it would appear that the -material was precipitated by the action of bacteria. Such for instance -is probably the origin of the Clinton iron ore, a bed of oolitic -hematite, extending from New York State all down the Appalachian -Mountains to Alabama. - - -Pisolite -Pl. 69 - -When the concretions, formed in exactly the same manner as in the case -of oolite, are of a size bigger than a pea, then the rock is known as -pisolite. - - - Other Concretions - -Though less abundant concretion may form from still other substances. -Hematite has been mentioned, and when concretions are made of this -material, either they have been deposited by bacteria, or were formed as -limonite and the water of crystallization of this latter mineral driven -off. - -Manganese concretions are found on the floor of the ocean at maximum -depths, and brought to the surface by dredging. - - - Geodes - -Geodes are nodules, which, when broken open, are found to be hollow and -the cavity lined with one or more minerals. They represent a special -case of minerals in a cave. There was in the first place a cavity in the -surrounding rock, usually of sand or clay. As the water leached through -the surrounding rock, it became saturated with one or more minerals and -then coming into the cavity, deposited the minerals, either as crystals, -or as a non-crystalline mass, lining the cavity. Thus the inside is -often a beautiful cluster of bristling crystals, or it may be simply -layer on layer of chalcedony of any color. Before this process had gone -so far as to completely fill the cavity, erosion had dislodged the mass, -and it has been found. One usually recognizes that it is a geode by the -fact that it is far too light to be a solid rock, and then it may be -carefully broken. They are characteristic of certain formations; so that -having accidentally broken the first one, others can be carefully opened -to display the beauty of the interior. The geode illustrated on Plate 70 -is lined with quartz crystals, but near by were found many others, some -of which had chalcedony and some jasper as a lining. Such crystallined -nodules are usually called geodes so long as they occur in a softer -matrix so that they are easily dislodged, and until they reach a size of -three or four feet in diameter. - - - Pebbles - -When picked up either from brook beds, sea beaches, or the open plain, -there are few forms of rock which tell a story of the past more -completely than do pebbles; and any one, who enjoys reading a story -written in form, structure and composition, will find in pebbles one of -the most satisfying and at the same time testing exercises. The story -may be complex or simple according to what has happened to the parent -rock, and to that is added what happened since the pebble left the ledge -where it was a part of a great mass. One must not forget to take into -consideration where the pebble was found and the character of its -associates. This sort of exercise is recommended to all interested in -rocks. It will yield something upon first trying, and more on prolonged -study; and the fullness with which it is done will test one’s knowledge -of the meaning of rocks as nothing else will do. As a sample of this -sort of exercise let us take the two pebbles illustrated on Plate 71. - -The upper one is a common quartz pebble picked up in a New England brook -bed. Such pebbles are common all over the country formerly covered by -the glacial ice sheet. It is crystalline quartz, but the individual -crystals are not distinguishable, and such quartz is typical as the -filling of veins. It therefore goes back to a time when the rocks were -fissured, probably in connection with the folding accompanying mountain -making far to the north in Canada. Into the fissures thus formed seeped -the water which had been leaching through the adjacent rocks, and it was -saturated with silica which it had dissolved from those rocks. In the -open fissure the quartz was deposited as crystals, which grew finally -filling the fissure and crowding each other so that all the faces were -obliterated. The quartz vein was complete, but it must have been far -below the surface of the ground. Time must have passed, thousands of -years of it, until, in the weathering away of the mountain system, the -many feet of overlying rock were removed and this vein was brought to -the surface. As the quartz is harder than the adjacent rocks, the vein -soon projected as a ledge. The effect of changes of temperature in -alternately expanding and contracting the rocks developed cracks, into -which water worked its way, and then the breaking was hastened by the -expansion which takes place when water freezes, and in exposed regions -is so effective, because the freezing and thawing are so often repeated. -Finally an angular fragment of quartz was dislodged and lay on the -surface, resistant to the solvent power of the rain. In this case this -happened just before the advance of the great ice sheet. When that came -to the place where the fragment lay, it was picked up along with all -other loose material and partly shoved in front of, but probably mostly -carried frozen in the ice, and journeyed one, two, three hundred, -perhaps a thousand miles. This took many years for the ice moved only a -few feet a day. Finally however it came to the point where the ice -melted as fast as it advanced, and our quartz fragment was dropped at -the front of the ice sheet along with other great masses of till. Here -there was abundant water, partly from the melting of the ice, and partly -from the storms which must develop where there are such contrasts in -temperature, as there would be over the ice, on one hand, and over the -bare land in front of the ice on the other hand. A torrent picked up our -fragment and started it on a second journey, banging against other -stones as it rolled along down the stream bed, every time it struck -another stone bruising the corners which soon became rounded. Thus from -time to time during high water the quartz fragment, becoming rounder -every time it moved, journeyed down stream, until it came to the point -where the stream emptied into a lake. Here the current was checked and -the stone dropped to the bottom along with other larger stones to make -the delta at the mouth of the stream. There it lay as long as the lake -existed, and would be lying now, but that in New England a tilting -movement of the land tipped the north end of the lake up and the water -all ran out. Then the stream began to flow over its own delta and in -time of freshet tore a channel down through the old delta carrying the -pebble still further down, until it came to the level stretch which -represented the old lake’s bottom and there it dropped the pebble in its -bed. And there it was found and picked up to become the pebble which -told the above story of its life, and to repeat it as often as anyone -will look at it with a seeing eye. - - -The second pebble is quite a different one. It was picked up in a gravel -bank along a railroad cut, just at the foot of Mt. Toby in -Massachussetts, and the writer has used it many times to test his -students, to see if they could read the story which it tells. - -It consists of two sorts of rock, the one, angular fragments of a -hornblende schist, the other, a fine-grained granite filling all the -spaces between the fragments of schist, even in cracks less than a -quarter of an inch wide. The schist is the older rock and in its first -appearance represents a deposit of mud (clay and sand) on the floor of -the ocean, well out from the shore, and somewhere off to the east of Mt. -Toby, perhaps ten miles, perhaps more, from the place where it was -found. This was back in early Palæozoic times, millions of years ago. - -This deposit was buried by further layers of sediment on the sea bottom -and cemented into a shale. Then during a mountain making period the -region was folded, and the sediments were altered by the combined -pressure and heat, our layer of rock becoming a hornblende schist. After -that happened considerable time must have passed, but just how much is -not indicated by the pebble, before another period of disturbance took -place, during which this deep seated schist was faulted, and shattered -to fragments along the line of breaking. This accounts for the angular -fragments. Then into the fissure thus formed was pressed a molten magma, -which while liquid enough to flow and be squeezed into every opening -could not have been very hot; for not even the corners of the schist -fragments are melted or altered, so as to appear any different from the -mass of the schist. The molten magma cooled rather slowly, making a -fine-grained granite. This must all have taken place far below the -surface, or the magma would have cooled into a felsite or dense lava. - -Again a long time must have elapsed, while the rock overlying our piece -was eroded away, so it could come to the surface. Just about the time it -did come to the surface, the Connecticut Valley was formed by a great -block, 95 miles long by fifteen to twenty miles wide, dropping down six -or eight thousand feet (probably not all at once but by one or two -hundred feet at a time) between two north and south faults. This took -place in the Triassic Period. Of course the streams then began to wash -sand and stones of all sizes into the hole. Our pebble was one of these. -While still an angular fragment, lying perhaps ten miles east of the -Connecticut Valley, a stream started it moving, and as it rolled along -the brook bed, it was battered and rounded to its present shape, and -finally tumbled over a waterfall to the bottom of the great hole, which -had been formed as described above. Here with other stones it formed -part of a coarse gravel, coarsest near the sides of the hole, and finer -toward the middle; for the material was further distributed in the -bottom of the valley. Our stone stayed pretty near the side and was soon -buried beneath hundreds of feet of similar material. The leaching water -dissolved enough iron rust so that this acted on the lower layers as a -cement and bound the whole mass into a conglomerate. - -Here for some millions of years our pebble rested, while above it was -piled sand and gravel and a couple of sheets of lava, until the hole was -filled, and our pebble was near the bottom of the mass. Later movements -of the land raised the whole region, fully six thousand feet, and -erosion went on for other millions of years. The conglomerate and -sandstone wore away faster than the metamorphosed rocks on either side -of the filled valley, so that a new valley, the present Connecticut -Valley, came into existence. - -When our pebble finally came near to the surface on the side of Mt. Toby -(a mound of conglomerate which somehow was protected and wore down a -little less rapidly than the conglomerate on either side of it), it was -just about the time of the glacial period. The great ice sheet went over -the mountain removing all the loose material and some more of the solid -conglomerate. This brought our pebble to the surface, but too late to be -moved by the ice. However as soon as the ice left the Mt. Toby region, -the rains fell, and in the further weathering of the conglomerate, the -cement holding our pebble in place was dissolved and it was freed. At -once a tiny brook started it rolling down the side of the mountain, a -brook so small that when the pebble reached the foot of the slope it did -not have power to carry it further. Here there gathered a fan-shaped -mound of such pebbles, known as an alluvial fan. It rested here not over -a couple of thousand years, when the Central Vermont R. R. cut a groove -through the fan, using the material for ballast, and here the pebble was -found and brought home. - - - Meteorites - -Meteorites can hardly be called common, but there is always a chance of -finding one, and their interest is so great, that none should escape -because unrecognized. - -Meteorites are visitors to the earth from space, and they bring to us -knowledge of the composition of planets and solar systems, other than -our own. It is of interest to note, that while they have brought to us -some combinations of elements which do not occur in the earth, still -they have not brought any element with which we were not already -familiar. They are popularly known as “falling” or “shooting stars,” -though of course they are not stars, but only small masses of matter -which are entirely invisible until they come inside our atmosphere. - -In space there are many small (compared with the size of the earth) -chunks of matter, each pursuing its solitary way around the sun, or -wandering through space along paths entirely unrelated to the sun. From -time to time one of these passes near enough to the earth, so as to be -influenced by its attraction, and then comes rushing toward it at -tremendous speed, 20 to 30 miles per second. As soon as it comes into -the atmosphere, even the very attenuated atmosphere, a couple of hundred -miles above the surface, friction heats the surface of the meteor until -it glows, and by that light we see the so-called shooting star, often -with a trail of luminous matter streaming out behind. Of course in using -this term “shooting star,” we understand the meteor is no star, for they -are bodies as big as our sun, shining at distances billions of miles -away. - -As the meteor rushes through the atmosphere it may all burn up, no large -fragment reaching the earth’s surface. The luminous matter streaming out -behind is material which has melted and dripped off the main mass. As -this oxidizes and cools, that part which did not become gaseous will -finally fall to the earth as fine dust. When however a meteor actually -falls to the earth, its surface is still hot, though probably there has -not been time enough for much heat to be transmitted to the interior. At -any rate they do not show any alteration due to this cause. On landing -and sometimes before they land meteors break into two or more pieces. -When found the surface always shows the effects of the heat generated by -the friction of passing through the air, the surface being smoothed, and -covered with stream lines and melted out pits and hollows, and the outer -surface consisting of a thin crust, making an appearance, which once -seen, can hardly be mistaken. - -There are two types of meteorites, those made wholly or largely of iron -with some nickel, and appearing like great chunks of iron, and those -which are stony and resemble a granite boulder. In collections the first -sort, _i.e._ iron meteorites, are most abundantly represented, because -most easily recognized when found. They consist of masses of iron and -nickel with small amounts of other elements, ranging in size from the -Cape York meteorite, which fell in northern Greenland in 1894 and was -later brought by Peary to the American Museum, and weighs some 36 tons, -down to small grains as small as a grain of wheat. The largest one which -has fallen in the United States was the Willamette meteorite weighing -some 15 tons, and falling 19 miles south of Portland, Oregon. These and -all iron meteorites have the iron in crystalline form which is readily -seen if the meteorite is cut, and the surface thus made polished, then -etched with acid, which is put on and quickly washed off. Every -meteorite has its particular pattern, as illustrated on Plate 72, and by -these patterns can be identified. Meteorites have a high value and are -eagerly sought by certain large institutions and collectors. Since the -crystalline structure is so characteristic of each fall, when a new -meteorite is found, it is usually cut in two, and one part retained by -the finder or some institution; while the other part is cut into small -pieces, an inch or two on a side and a quarter of an inch thick, but -each large enough to show the characteristic pattern. These are -distributed largely by sale to other collectors. Thus a great meteorite -collection consists of a few large meteorites and a great many small -portions of other meteorites. - -The second type of meteorite is the stony meteorite. Where meteorites -have been located as they fell and recovered, the majority of them were -of this type, so that probably more than half of the meteorites which -fall are of the stony type. However when the stony meteorite is exposed -to weathering it takes only a very short time before the surface is -eroded off and then such a meteorite looks like any other boulder and -probably most of them fail to be recognized, and so have been lost. -Because they have so much greater variety, they are in many ways of -greater interest than the iron type. - -It is desirable that every one have his eye out for meteorites, and when -found it is desirable that the fact should be reported to some one of -the great institutions which collect them, such as the National Museum -in Washington, or the American Museum in New York. Each one should be on -record even if it is desired to keep it in a private collection. - - - Fossils - -In the sedimentary rocks one is apt to find remains of some of the -animals and plants that lived at the time the rock was forming. While -the soft parts of animals decompose rapidly, shells and bones are likely -to be buried in the sediments, and if the conditions have been -favorable, these remains may be preserved more or less perfectly. All -through the millions of years that sedimentary rocks have been forming -in the sea, in lakes, on river flood plains and in wind swept deserts, -there was an abundance of life, as much as there is today; and our -knowledge of that life is derived from these buried fossil remains, so -that fossils have a great historic interest. - -However as there have lived and died several times as many different -kinds of animals as live today, the study of fossils becomes a separate -subject, which cannot be treated in this book. Should any collector of -rocks and minerals come upon fossils, he is opening a new field, and it -will be necessary to turn to other sources for their identification. -General books on this subject are scarce, but one or two are given in -the literature list. - - - A List of the Elements, the Abbreviations Used for Them, and Their - Atomic Weight, Which Is Approximately the Number of Times Heavier They - Are Than Hydrogen. - - Name Oxygen = 16 - - Aluminium, Al 27 - Antimony, Sb 122 - Argon, Ar 40 - Arsenic, As 75 - Barium, Ba 137 - Beryllium, Be 9 - Bismuth, Bi 209 - Boron, B 11 - Bromine, Br 80 - Cadmium, Cd 112 - Cæsium, Cs 132 - Calcium, Ca 40 - Carbon, C 12 - Cerium, Ce 140 - Chlorine, Cl 35 - Chromium, Cr 52 - Cobalt, Co 59 - Columbium, Cb 93 - Copper, Cu 64 - Dysprosium, Dy 162 - Erbium, Er 167 - Europium, Eu 152 - Fluorine, F 19 - Gadolinium, Gd 157 - Gallium, Ga 70 - Germanium, Ge 63 - Glucinum, Gl 9 - Gold, Au 197 - Hafnium, Hf 179 - Helium, He 4 - Holmium, Ho 165 - Hydrogen, H 1 - Indium, In 115 - Iodine, I 127 - Iridium, Ir 193 - Iron, Fe 56 - Krypton, Kr 84 - Lanthanum, La 139 - Lead, Pb 207 - Lithium, Li 7 - Lutecium, Lu 175 - Magnesium, Mg 24 - Manganese, Mn 55 - Mercury, Hg 201 - Molybdenum, Mo 96 - Neodymium, Nd 144 - Neon, Ne 20 - Nickel, Ni 59 - Nitrogen, N 14 - Osmium, Os 190 - Oxygen, O 16 - Palladium, Pd 107 - Phosphorus, P 31 - Platinum, Pt 195 - Potassium, K 39 - Præseodymium, Pr 141 - Protoactinium, Pa 231 - Radium, Ra 226 - Radon, Rn 222 - Rhenium, Re 186 - Rhodium, Rh 103 - Rubidium, Rb 85 - Ruthenium, Ru 102 - Samarium, Sm 150 - Scandium, Sc 45 - Selenium, Se 79 - Silicon, Si 28 - Silver, Ag 108 - Sodium, Na 23 - Strontium, Sr 88 - Sulphur, S 32 - Tantalum, Ta 181 - Tellurium, Te 128 - Terbium, Tb 159 - Thallium, Tl 204 - Thorium, Th 232 - Thulium, Tu 169 - Tin, Sn 119 - Titanium, Ti 48 - Tungsten, W 184 - Uranium, U 238 - Vanadium, V 51 - Xenon, Xe 131 - Ytterbium, Yt 173 - Yttrium, Y 89 - Zinc, Zn 65 - Zirconium, Zr 91 - - - Table of Geologic Time - - _Eras_ - _Periods and their _Important Physical _Important - Duration in Millions Events_ Organic Events_ - of Years_ - - Cenozoic - Quaternary - Recent Youthful land forms Dominance of man. - having high relief - formed. - Pleistocene Epoch 2 M.Y. Period of Heidelberg, - glaciation; four Neanderthal, and - great ice advances. Crô-Magnon man; - extinction of - large mammals. - Tertiary - Pliocene Epoch 10 M.Y. Continuing Intermigration of - world-wide land North and South - elevation. American mammals. - Transformation of - ape to man. - Miocene Epoch 18 M.Y. Cordilleras, Alps, Culmination of - Himalayas formed. modern types of - Widespread mammals. Apes - vulcanism-basalt appear in Old - flows in World. - northwestern United - States. - Oligocene Epoch 10 M.Y. Land dominant; seas Carnivores and - marginal. ungulates develop - into importance. - Eocene Epoch 20 M.Y. Extensive Dawn of the - sedimentation; seas dominance of - marginal. mammals. Reptiles - subordinate. - Cretaceous 65 M.Y. Widespread Climax and - epicontinental culmination of - seas. Laramide reptiles, - revolution at close especially - of period—Rocky dinosaurs; first - Mountains formed. flowering plants - and grasses. - Mesozoic - Jurassic 38 M.Y. Continent emergent; Rise of birds and - shallow seas on flying reptiles, - western North first modern - America. trees. - Triassic 35 M.Y. Continent emergent; Rise of - seas marginal. dinosaurs, - cycads, and - ammonites. - Paleozoic - Permian 35 M.Y. World-wide Extinction of - continental uplift most Paleozoic - and mountain fauna and flora. - building. First modern - Widespread insects. - glaciation. - Pennsylvanian 48 M.Y. Continent Great - alternately rising coal-forming - and sinking. forests, of ferns - and seed-ferns. - Mississippian 35 M.Y. Low lands and Culmination of - widespread crinoids, - submergence. numerous sharks. - Devonian 40 M.Y. Widespread First known land - submergence, local animals, first - vulcanism. forests. - Silurian 28 M.Y. Widespread First lung fishes - submergence, local and scorpions, - deserts. abundant corals. - Ordovician 65 M.Y. 60% of North Climax of - America below sea. invertebrate - dominance, first - vertebrate. - Cambrian 105 M.Y. Widespread First abundant - submergence. invertebrate - fauna, trilobites - dominant. - Proterozoic 700 ± M.Y. Long periods of Bacteria and - granite intrusion, seaweeds present. - sedimentation, and Most - mountain building. invertebrates - probably present, - but remains are - lacking. - Archeozoic 800 ± M.Y. World-wide Blue-green algae - intrusive igneous present, - activity; some primitive - sediments. one-celled plants - and animals - probably present. - - - - - BIBLIOGRAPHY - - - MINERALOGY - -_Getting Acquainted with Mineralogy._ By G. L. English, 1936, - McGraw-Hill Book Co. A beginning textbook of mineralogy. - -_Introduction to the Study of Minerals and Rocks._ 3rd Edition, by A. F. - Rogers, 1937, McGraw-Hill Book Co. Describes the commoner minerals - systematically. - -_Dana’s Textbook of Mineralogy._ 4th Edition, revised by W. E. Ford, - 1932, John Wiley and Sons. Detailed descriptions of minerals, their - physical properties, and their occurrence. - -_Manual of Mineralogy._ 15th Edition, by E. S. Dana, revised by C. S. - Hurlburt, 1941, John Wiley and Sons. A textbook of mineralogy. - - - MINERAL ECONOMICS, GEOPOLITICS - -_World Minerals and World Peace._ By C. K. Leith, J. W. Furness, and - Cleona Lewis, 1943, The Brookings Institution. Physical, economic, - and political trends in the mineral industry. - -_Minerals in World Affairs._ By T. S. Lovering, 1943, Prentice-Hall. - -_Minerals Yearbook._ U. S. Bureau of Mines. An annual volume presenting - statistical data on the production of the mineral resources of the - United States. Reports on individual minerals or rocks may be had - separately. - - - ECONOMIC GEOLOGY - -_Mineral Deposits._ 4th Edition, by W. Lindgren, 1933, McGraw-Hill Book - Co. The manner of occurrence and origin of mineral deposits. - -_Elements of Engineering Geology._ 2nd Edition, by H. Ries and T. L. - Watson, 1947, John Wiley and Sons. - -_This Fascinating Oil Business._ By M. W. Ball, 1940, Bobbs-Merrill Co. - A simple and elementary description of the petroleum industry. - -_Geology of Coal._ By O. Stutzer and A. C. Noe, 1940, University of - Chicago Press. - - - GENERAL GEOLOGY - -_Down to Earth._ By C. Croneis and W. C. Krumbein, 1936, University of - Chicago Press. An introduction to geology, profusely illustrated. - -_Textbook of Geology Part I—Physical Geology._ 4th Edition, by C. R. - Longwell, A. Knopf, and R. F. Flint, 1939, John Wiley and Sons. A - standard text on geology. - -_Field Geology._ 4th Edition, by F. H. Lahee, 1941, McGraw-Hill Book Co. - Recognition and interpretation of geologic structures and - topographic forms as they are observed, and methods of geologic - work. - - - PRECIOUS STONES - -_A Book of Precious Stones._ By J. Wodiska, 1910, G. P. Putnam’s Sons. - Written for jewelers, but of general interest. - -_The Curious Lore of Precious Stones._ By G. F. Kunz, 1913, Lippincott. - Legends and stories of the gem minerals. - -_The Magic of Jewels and Charms._ By G. F. Kunz, 1915, Lippincott. - -_Popular Gemology._ By R. M. Pearl, 1948, John Wiley and Sons. - Scientific and industrial uses of gems, current information about - their locality and production. - - - FOSSILS - -_An Introduction to the Study of Fossils._ By H. W. Shimer, 1933, - Macmillan Co. An introductory textbook about fossil plants and - animals. - -_Invertebrate Paleontology._ By W. H. Twenhofel and R. P. Shrock, 1935, - McGraw-Hill Book Co. - -_Textbook of Geology Part II—Historical Geology._ 4th Edition, by C. - Schuchert and C. O. Dunbar, 1941, John Wiley and Sons. The story of - the development of life through the ages. - - - - - INDEX - - - A - Actinolite, 120 - Adobe, 210 - Agate, 107 - Agate, moss, 73, 108 - Alabaster, 152 - Albertite, 229 - Albite, 110, 113, 115 - Almandine, 97 - Almandite, 122, 123 - Aluminum bronze, 74 - Aluminum group, 73 - Amazon stone, 114 - Amber, 223 - Amethyst, 104 - Amethyst, Oriental, 75 - Amianthus, 120 - Amphibole group, 119 - Amygdoloid, 194 - Amygdoloidal, 176 - Analcite, 141 - Andesite, 113, 187 - Andradite, 122, 124 - Anglesite, 62 - Anhydrite, 149 - Anorthite, 110, 113 - Anorthosite, 183 - Anthracite, 218, 222 - Antimony, 81 - Antimony, gray, 81 - Apatite, 160 - Aquamarine, 125 - Aragonite, 147 - Argentite, 35 - Argillite, 242 - Arkose, 206 - Arsenic group, 78 - Arsenopyrite, 79 - Asbestos, 120, 140 - Augite, 118 - Aventurine, 104 - Azurite, 46 - - - B - Barite, 154 - Barium group, 154 - Basalt, 188 - Batholith, 174 - Bauxite, 77 - Beryl, 125 - Beryl, golden, 125 - Beryllium, 125 - Bibliography, 270 - Biotite, 129, 130 - Bitumen, 228 - Black jack, 65 - Bloodstone, 106 - Bog lime, 213 - Bombs, 191 - Boracite, 164 - Borax, 165 - Bornite, 41 - Brass, 64 - Breccia, 191, 198 - Brittania metal, 81 - Bronze, 38 - Bronze Age, 38 - Bronzite, 118 - Bytownite, 113 - - - C - Calamine, 68 - Calaverite, 30 - Calcite, 144 - Calcium, 143 - Carbon, 156 - Carbonite, 222 - Carbuncle, 124 - Carnelian, 106 - Carnotite, 90 - Cassiterite, 93 - Cat’s eye, 104 - Celestite, 153 - Cerargyrite, 37 - Cerrusite, 61 - Ceylonite, 97 - Chalcedony, 104, 106 - Chalcocite, 42 - Chalcopyrite, 40 - Chalcotrichite, 45 - Chalk, 213 - Chert, 107 - Chlorite, 140 - Chlorospinel, 98 - Chromite, 87 - Chromium, 86 - Chrysocola, 47 - Chrysolite, 134, 140 - Chrysoprase, 106 - Cinnabar, 91 - Cinnamon stone, 123 - Citrine, 103 - Clay, 207 - Clay, ball, 208 - Clay, brick, 209 - Clay, china, 208 - Clay, fire, 208 - Clay, paving brick, 209 - Clay, sewer-pipe, 209 - Clay, slip, 209 - Clay, stoneware, 209 - Clay stones, 250 - Cleavage, 21 - Cleavage, slaty, 234 - Coal, 217 - Coal, bituminous, 212, 220 - Coal, cannel, 221 - Coal, hard, 222 - Coal, soft, 220 - Cobalt, 84 - Cobalt bloom, 85 - Cobalt glance, 85 - Cobalt gray ore, 85 - Cobaltite, 83 - Coke, 220 - Colemanite, 165 - Collecting, 5, 7 - Color, 23 - Concretions, 248 - Concretions, flint, 253 - Concretions, lime, 251 - Concretions, other, 255 - Concretions, sandstone, 253 - Conglomerate, 202 - Copper, 37, 39 - Copper, blushing, 42 - Copper, glance, 42 - Copper, grey, 43 - Copper, peacock, 42 - Copper, plush, 45 - Copper, purple, 41 - Copper, red, 44 - Copper, variegated, 42 - Copper, yellow, 40 - Coquina, 213 - Coral, 146 - Coral rock, 214 - Corundum, 75 - Crude oil, 227 - Cryolite, 78 - Crystal balls, 101 - Crystal formation, 14 - Crystal rock, 103 - Crystal structure, 11 - Crystal systems, 13-18 - Cuprite, 44 - Cyanite, 128 - - - D - Dacite, 187 - Dense, 176 - Diamond, 157 - Diamonds, Matura, 127 - Diamonds, slave’s, 133 - Diatoms, 231 - Dikes, 174 - Diorite, 182 - Dog-tooth spar, 145 - Dolomite, 99 - Dry bone, 68 - - - E - Earth, diatomaceous, 23 - Elements, listed, 267 - Emerald, 125 - Emerald, Oriental, 75 - Emery, 76 - Enstatite, 117 - Epidote, 134 - Equipment, 7 - Erubescite, 42 - Extrusive, 173 - - - F - Feldspar, 110 - Feldspar, alkalic, 111 - Felsite, 186 - Felsitic, 176 - Ferromanganese, 70 - Flagstone, 207 - Flint, 106 - Fluorine, 162 - Fluorite, 162 - Fossils, 266 - Fragmental, 176 - Franklinite, 69 - Freestone, 207 - - - G - Gabbro, 183 - Galena, 60 - Garnet group, 121 - Garnet, Sirian, 123 - Geodes, 255 - German silver, 82 - Gilsonite, 229 - Glassy, 176 - Glucinum, 125 - Gneiss, 237 - Goethite, 51, 52 - Gold, 31 - Gold foil, 64 - Gold group, 29 - Gossan, 50 - Granite, 178 - Granite, graphic, 179 - Granitoid, 176 - Graphite, 156, 219 - Gravel, 201 - Graywacke, 206 - Grit, 206 - Grossularite, 122, 123 - Guano, 230 - Gumbo, 210 - Gypsum, 150 - - - H - Halite, 163 - Hardness, 20 - Hardpan, 216 - Heavy spar, 154 - Heliotrope, 106 - Hematite, 53 - Hemihedral forms, 19 - Hercynite, 98 - Hexagonal system, 18 - Hornblende, 121 - Hornstone, 107 - Hyacinth, 127 - Hypersthene, 118 - - - I - Ice, 167 - Iceland spar, 145 - Ice stone, 78 - Ilmenite, 94 - Intrusive, 174 - Iron, 47 - Iron, bog, 50 - Iron, chromic, 87 - Iron, magnetic, 54 - Iron pyrites, 56 - Iron, spathic, 55 - Iron, specular, 53 - Isometric system, 13 - - - J - Jacinth, 127 - Jargons, 127 - Jargoons, 127 - Jasper, 106 - Jet, 222 - - - K - Kaolin, 137, 208 - Kaolinite, 137 - - - L - Labels, 5 - Labradorite, 113, 116 - Laccolith, 174 - Lapilli, 191 - Lava, 173 - Lead, 59 - Lead glance, 60 - Lead, green ore, 63 - Lead, white ore, 61 - Lepidolite, 129, 130 - Lignite, 218, 219 - Limestone, 212 - Limestone, encrinal, 214 - Limestone, hydraulic, 214 - Limestone, lithographic, 214 - Limonite, 49, 51 - Loess, 210 - Luster, 23 - - - M - Magma, 173 - Magnesite, 98 - Magnesium group, 96 - Magnetite, 54 - Malachite, 45 - Malanite, 124 - Malta, 229 - Manganese group, 70 - Manganite, 72 - Marble, 243 - Marble, Suisun, 146 - Marcasite, 57 - Marl, 211 - Mercury, 90 - Meteorites, 262 - Mica group, 128 - Microcline, 113, 114 - Millerite, 83 - Mineral tables, 25 - Minerals, defined, 10 - Molybdenite, 81 - Molybdenum, 80 - Monoclinic system, 17 - Monzonite, 181 - Morion, 103 - Mother-of-pearl, 148 - Muscovite, 129 - - - N - Natrolite, 142 - Natural gas, 227 - Needle iron stone, 52 - Niccolite, 83 - Nickel, copper, 83 - Nickel group, 82 - - - O - Obsidian, 191 - Ochre red, 54 - Ochre yellow, 49 - Oligoclase, 113, 115 - Olivine, 134 - Olivine-gabbro, 183 - Onyx, 108 - Onyx, Californian, 146 - Onyx marble, 215 - Onyx, Mexican, 146 - Oolites, 254 - Opal, 108 - Opal-agate, 109 - Opal, common, 109 - Opal, fire, 109 - Opal, precious, 109 - Ophicalcite, 246 - Ophiolite, 246 - Orpiment, 80 - Orthoclase, 110, 113 - Orthorhombic system, 16 - - - P - Paste, 103 - Pearls, 148 - Pearlstone, 193 - Peat, 218, 219 - Pebbles, 256 - Pegmatite, 179 - Peridot, 134 - Peridotite, 184 - Perlite, 193 - Petroleum series, 224, 227 - Pewter, 60 - Phenocrysts, 189 - Phlogopite, 129, 131 - Phosphate, 160, 230 - Phosphorus, 159 - Phyllite, 242 - Picotite, 97 - Pisolite, 255 - Pitchstone, 193 - Plagioclase, 111 - Plasma, 106 - Platinum, 95 - Plumbago, 156 - Porous, 176 - Porphyritic, 176 - Porphyry, 189 - Prase, 104 - Prousite, 36 - Psilomelane, 72 - Pumice, 193 - Pyrargyrite, 35 - Pyrite, 56 - Pyrite, capillary, 83 - Pyrite, magnetic, 58 - Pyrite, white, 57 - Pyritohedron, 56, 318 - Pyrolusite, 71 - Pyromorphite, 63 - Pyrope, 122, 123 - Pyroxene group, 116 - Pyroxenite, 185 - Pyrrhotite, 58 - - - Q - Quartz, 100 - Quartz-diorite, 181 - Quartz, milky, 103 - Quartz, rose, 104 - Quartz, smoky, 103 - Quartzite, 239 - Quicksands, 204 - Quicksilver, 90 - - - R - Radium, 89 - Realgar, 80 - Rhinestones, 101 - Rhodochrosite, 73 - Rhyolite 185 - Rock, phosphate, 230 - Rocks, 170 - Rocks, defined, 10 - Rocks, igneous, 172 - Rocks, igneous, classified, 177 - Rocks, metamorphic, 232 - Rocks, metamorphic, classified, 236 - Rocks, sedimentary, 194 - Rocks, sedimentary, classified, 196 - Rubicelle, 97 - Ruby, 75 - Ruby, Balas, 97 - Ruby mica, 52 - Rutile, 94 - - - S - Salt, 163 - Sand, 202 - Sandstone, 205 - Sapphire, 75 - Sapphire, Oriental white, 75 - Sardonyx, 108 - Satin spar, 146 - Schist, 240 - Schistosity, 234 - Scoria, 192, 193 - Septeria, 252 - Sericite, 130 - Serpentine, 139, 245 - Shale, 210 - Shale, oil-bearing, 225 - Sheet, 173 - Siderite, 55 - Silica, 99 - Silicates, 99 - Silicon, 99 - Sill, 174 - Sillimanite, 128 - Silver, 34 - Silver, dark red, 35 - Silver, German, 65 - Silver glance, 35 - Silver group, 32 - Silver, horn, 37 - Silver, light red, 36 - Silver, ruby, 35 - Sinter, 110 - Slate, 241 - Smalt, 84 - Smaltite, 85 - Smithsonite, 68 - Soapstone, 244 - Sodalite, 126 - Soil, 198 - Solder, 60 - Specific gravity, 22 - Speigeleisen, 70 - Spelter, 64 - Spessartite, 122, 123 - Sphalerite, 65 - Spinel, 97 - Spinel-ruby, 97 - Stalactites, 146 - Stalagmites, 146 - Staurolite, 133 - Steatite, 244 - Stellite, 84, 88 - Stibnite, 81 - Stilbite, 143 - Stock, 174 - Streak, 23 - Strontianite, 152 - Strontium group, 152 - Sulphur, 166 - Syenite, 180 - Sylvanite, 30 - - - T - Talc, 138 - Talus, 197 - Tetragonal system, 15 - Tetrahedrite, 43 - Tile ore, 45 - Till, 215 - Tillite, 217 - Time chart, 268 - Tin, 92 - Tin stone, 93 - Titanium, 93 - Tonalite, 181 - Topaz, 131 - Topaz, false, 103 - Topaz, Oriental, 75 - Topaz, Saxon, 132 - Topaz, Scotch, 132 - Topaz, smoky, 132 - Topaz, Spanish, 132 - Tourmaline, 135 - Trachite, 186 - Trap, 188 - Travertine, 146, 215 - Tremolite, 120 - Triclinic system, 18 - Tripolite, 110 - Tufa, calcareous, 147 - Tuff, 190 - Tungsten, 87 - Turgite, 51 - Turquois, 161 - Twinning, 19 - Type metal, 60 - - - U - Uintaite, 229 - Uranium, 89 - Uvarovite, 122, 123 - - - V - Vanadium, 89 - Verde antique, 247 - Volcanic ash, 190 - Volcanic blocks, 191 - - - W - Water, 167 - White metal, 64 - Willemite, 67 - Witherite, 153 - Wolframite, 88 - Wood, agatized, 108 - Wood, opalized, 109 - Wood, silicified, 108 - - - X - Xanthosiderite, 51 - - - Z - Zeolites, 141 - Zinc, 63 - Zinc blende, 65 - Zinc red ore, 66 - Zinc, ruby, 65 - Zincite, 66 - Zircon, 127 - - -Plate Frontispiece - - [Illustration: Tourmaline crystals, growing amid feldspar crystals - in a cavity in granite, from Paris, Me.] - - -Plate 5 - - [Illustration: Gold in quartz, from California] - - -Plate 6 - - [Illustration: Native silver in calcite] - - [Illustration: Argentite, the black masses throughout the white - quartz] - - -Plate 7 - - [Illustration: Pyrargyrite as it appears after moderate exposure to - the light.] - - [Illustration: Crystal form of Pyrargyrite] - - [Illustration: Prousite as it appears after moderate exposure to the - light] - - -Plate 8 - - [Illustration: Native copper from Michigan] - - [Illustration: Chalcopyrite in tetrahedrons and an occasional - octahedron.] - - -Plate 9 - - [Illustration: Chalcocite crystals with the bluish tarnish] - - [Illustration: Tetrahedrite crystals] - - -Plate 11 - - [Illustration: Cuprite, the red crystals showing characteristic - color, other showing the green tarnish of malachite] - - [Illustration: Malachite (green) and azurite (blue), the two - minerals shown together as they very commonly occur] - - -Plate 12 - - [Illustration: Limonite] - - [Illustration: The crystal form in which goethite is found, _p_ is - the prism faces, _b_ and _c_ are faces formed by beveling the edges - of the prism, _o_ is the pyramidal face characteristic of the ends] - - -Plate 13 - - [Illustration: Hematite, Clinton iron ore, oolitic] - - [Illustration: Siderite crystals] - - -Plate 15 - - [Illustration: Pyrite crystals] - - [Illustration: Marcasite in concretionary form with radiate - structure] - - -Plate 17 - - [Illustration: Galena in crystals] - - [Illustration: Pyromorphite crystals (green)] - - -Plate 19 - - [Illustration: Sphalerite, some the normal yellow and some crystals - with the reddish tinge. (White is dolomite)] - - [Illustration: Zincite] - - -Plate 21 - - [Illustration: Smithsonite in yellow crystals] - - [Illustration: Franklinite in octahedral crystals] - - -Plate 24 - - [Illustration: Arsenopyrite, showing crystals massed so as to be - incompletely developed] - - [Illustration: Realgar as it usually occurs in powdery - incrustations] - - -Plate 25 - - [Illustration: Large crystal of stibnite, the light colored face is - the one parallel to which cleavage occurs] - - [Illustration: Niccolite as a vein in slate] - - -Plate 26 - - [Illustration: Cobaltite, silver color, with pink tinge] - - [Illustration: Smaltite, pink is cobalt bloom] - - -Plate 27 - - [Illustration: Carnotite from southwest Colorado] - - [Illustration: Cinnabar] - - -Plate 31 - - [Illustration: Amethyst, not however deep enough colored for gems] - - [Illustration: Jasper, with botryoidal surface] - - -Plate 32 - - [Illustration: Banded Agate from Brazil] - - -Plate 33 - - [Illustration: Common Opal from Arizona] - - [Illustration: Siliceous sinter or Geyserite from The Yellowstone - Park] - - -Plate 35 - - [Illustration: A group of Microcline crystals from Pike’s Peak, - Colo.] - - [Illustration: Labradorite, showing multiple twinning (the - striation), and the iridescent play of colors] - - -Plate 36 - - [Illustration: Crystal form of a pyroxene; _a_ and _b_ prism faces, - _m_ the beveled edge between two prism faces] - - [Illustration: Cross section of a pyroxene crystal showing the lines - of intersection of the two cleavage planes] - - [Illustration: Cross sections of pyroxenes, showing typical forms - taken by crystals] - - [Illustration: Augite crystals, in crystalline limestone] - - -Plate 38 - - [Illustration: The dodecahedron and the 24-sided figure - characteristic of garnets] - - [Illustration: The garnet, grossularite] - - [Illustration: The garnet alamandite] - - -Plate 39 - - [Illustration: Beryl of gem quality] - - [Illustration: Zircon in syenite] - - -Plate 40 - - [Illustration: Cyanite crystals in schist] - - [Illustration: A crystal of mica, showing basal cleavage] - - -Plate 41 - - [Illustration: Crystal form typical of topaz] - - [Illustration: A topaz crystal from Brazil] - - [Illustration: Crystal form typical of staurolite when simple] - - [Illustration: A typical twin of staurolite] - - -Plate 43 - - [Illustration: Serpentine] - - [Illustration: Chlorite] - - -Plate 49 - - [Illustration: Apatite crystals in crystalline calcite] - - [Illustration: The ends of apatite crystals showing common modes of - termination] - - -Plate 50 - - [Illustration: A group of fluorite crystals] - - [Illustration: A group of halite crystals] - - -Plate 61 - - [Illustration: Amber] - - [Illustration: Two bottles of petroleum, the left hand one with a - paraffin base, the right hand one with an asphalt base] - - -Plate 65 - - [Illustration: Mica schist, with garnets] - - [Illustration: Chlorite schist] - - -Plate 67 - - [Illustration: Serpentine, composed of serpentine, hematite, and - some calcite] - - -Plate 1 - - - Basal forms of the isometric system - - [Illustration: Cube] - - [Illustration: Octahedron] - - [Illustration: Dodecahedron] - - -Plate 2 - - - Basal forms of the tetragonal system - - [Illustration: A square prism] - - [Illustration: Octahedron] - - - Basal forms of the orthorhombic system - - [Illustration: A Rectangular prism] - - [Illustration: Octahedron] - - -Plate 3 - - - Basal forms of the monoclinic system - - [Illustration: The rectangular prism askew] - - [Illustration: The octahedron] - - [Illustration: A cross section of the prism with its edges beveled - so that the _b_ faces are obliterated by the _m_ faces, and a - six-sided prism is formed (pseudo-hexagonal)] - - [Illustration: Basal form of the triclinic system] - - -Plate 4 - - - Basal forms of the hexagonal system - - [Illustration: The six-sided prism] - - [Illustration: The double pyramid] - - [Illustration: The rhombohedron] - - -Plate 10 - - [Illustration: Tetrahedrons showing characteristic manner in which - tetrahedrite occurs] - - [Illustration: A cube with the edges beveled and the corners cut in - a form characteristic of cuprite] - - -Plate 30 - - [Illustration: Two intergrowing or twinned quartz crystals] - - [Illustration: Diagram of the typical quartz crystal, _p_ prism - faces, _l_ left hand rhombohedron, _r_ right hand rhombohedron] - - [Illustration: A quartz crystal on which the left hand rhombohedron - is represented by small faces while the right hand rhombohedron has - large faces] - - -Plate 14 - - [Illustration: Crystal forms of hematite, _A_ the rhombohedron with - the edges beveled; _B_ the tabular form, resulting from the - excessive development of the two _o_ faces opposite each other] - - [Illustration: A typical crystal of magnetite] - - [Illustration: The rhombohedron typical of siderite] - - -Plate 16 - - [Illustration: The pyritohedron] - - [Illustration: The pyritohedron with certain of its edges beveled by - the cube faces, to show the relationship of these two forms] - - -Plate 18 - - - Typical forms for cerrusite - - [Illustration: The pyramid, _n_ the prism face, _m_ the beveled - prism, _p_ the octahedral face, and _o_ the edge of the octahedral - faces beveled] - - [Illustration: The simple type of twinning] - - [Illustration: A multiple twin where three crystals grow through - each other] - - [Illustration: Forms in which anglesite occurs: _l_ the pyramid - face, _p_ the prism face, _o_ the vertical edge of the prism - beveled, _m_ the horizontal edge of the prism beveled, _n_ a further - beveling of the horizontal edge of the prism. _D_ the tabular, _E_ - the prismatic form] - - -Plate 20 - - [Illustration: A characteristic form in which sphalerite may occur; - being the combination of, _d_ the dodecahedron, _o_ the octahedron, - and _t_, a 24-sided figure] - - [Illustration: Characteristic form for zincite crystals, _n_ the - hexagonal prism, and _p_ pyramidal faces on it] - - [Illustration: Typical form of crystal of willemite: _p_ the prism, - _r_ rhombohedron faces on end, ½ _r_ a second lower rhombohedron] - - -Plate 22 - - [Illustration: Moss agates, showing the dendritic growth of - manganitic minerals, like manganite or pyrolusite] - - [Illustration: Moss agates] - - [Illustration: Crystal form of manganite] - - -Plate 23 - - [Illustration: Crystals of green corundum in syenite, from Montana] - - [Illustration: Typical crystal forms of corundum: _A_ the elongated - prism with the alternate corners cut by rhombohedral faces, _B_ the - tabular prism, _C_ the double pyramid] - - -Plate 28 - - [Illustration: Cassiterite, twinned crystals] - - [Illustration: The crystal form in which both cassiterite and rutile - occur when in simple crystals, _p_ prism faces, _m_ beveling of the - prism, _o_ octahedral face, _n_ beveling of the edge between - octahedral faces] - - [Illustration: Multiple twinning characteristic of rutile] - - -Plate 29 - - [Illustration: Crystal of Spinel] - - - Crystal forms in which dolomite occurs - - [Illustration: _A_ the cleavage form, rhombohedron with the faces - curved] - - [Illustration: _B_ the rhombohedron with the corners cut, as it - often occurs] - - [Illustration: _C_ the form found in gypsum or anhydrite] - - -Plate 34 - - [Illustration: Orthoclase, a cleavage piece, _a_ and _b_ the perfect - cleavage planes, and _c_ the imperfect cleavage plane] - - - Crystal forms of orthoclase - - [Illustration: _A_ the simple crystal] - - [Illustration: _B_ the twinned form] - - [Illustration: _C_ the twinned form in which the crystals are - intergrowing] - - [Illustration: Diagram of a multiple twin of a plagioclase feldspar] - - -Plate 37 - - - Diagrams of amphibole crystals - - [Illustration: _A_ a typical crystal] - - [Illustration: _B_ cross section showing the intersection of - cleavage planes] - - [Illustration: _C_ and _D_ cross sections to show variations in - outline] - - [Illustration: Tremolite in silky fibrous crystals. Asbestos] - - [Illustration: Hornblende crystals in quartzite] - - -Plate 42 - - [Illustration: Epidote crystals] - - [Illustration: Typical forms of epidote crystals; _p_ prism faces, - _m_, _n_, _x_, and _y_ beveled edges of the prism, _o_ octahedral - faces] - - - Typical forms of tourmaline - - [Illustration: _A_ side view; _B_ and _C_ ends to show terminations; - _p_ prism faces, _m_ beveling of prism edges, _r_ a low rhombohedron - on the end, _s_ the opposite rhombohedron, _b_ basal face, and the - other faces represent bevelings] - - -Plate 48 - - [Illustration: A group of barite crystals] - - [Illustration: Outline of the typical tabular barite crystal] - - [Illustration: The six-sided double pyramid, composed of three - interpenetrating crystals, typical of witherite and strontianite] - - -Plate 44 - - [Illustration: The typical form of analcite] - - [Illustration: A typical natrolite crystal] - - [Illustration: The typical crystal form of stilbite] - - [Illustration: A sheaf-like bundle of fibrous crystals, typical of - stilbite] - - -Plate 45 - - [Illustration: A group of calcite crystals] - - - Typical forms of calcite - - [Illustration: _A_ the rhombohedron formed by cleavage] - - [Illustration: _B_ a rhombohedral crystal truncated by the basal - plane] - - [Illustration: _C_ the scalenohedron] - - [Illustration: _D_ the scalenohedron truncated by the rhombohedron] - - [Illustration: _E_ the scalenohedron on a prism] - - -Plate 46 - - - Typical forms of aragonite - - [Illustration: _A_ the simple crystal] - - [Illustration: _B_ a needle-like form, twinned] - - [Illustration: _C_ cross section to show how the form may appear - six-sided] - - [Illustration: Typical form of the anhydrite crystal] - - -Plate 47 - - [Illustration: A piece of gypsum looking on the surface of the - perfect cleavage, and showing the two other cleavages as lines, - intersecting at 66°. Twinning is also shown] - - [Illustration: A simple crystal of gypsum] - - [Illustration: Twin crystals of gypsum] - - -Plate 51 - - [Illustration: Sulphur crystals] - - [Illustration: Ice crystals, the top one, the end of a hexagonal - prism; the two lower figures multiple twins as in snow flakes] - - -Plate 52 - - [Illustration: The Devil’s Tower, Wyoming, an example of igneous - rock with columnar structure, and resting on sedimentary rocks. - Courtesy of the U. S. Geological Survey] - - -Plate 53 - - [Illustration: A coarse granite] - - [Illustration: Graphic granite] - - -Plate 54 - - [Illustration: Syenite] - - [Illustration: Gabbro] - - -Plate 55 - - [Illustration: Basalt-porphyry. The large white crystals are - phenocrysts of plagioclase feldspar] - - [Illustration: Basalt-obsidian] - - -Plate 56 - - [Illustration: Amgydoloid] - - -Plate 57 - - [Illustration: The north face of Scott’s Bluff, Neb., showing - sedimentary sandstones above and clays below. The type of erosion is - characteristic of arid regions. Courtesy of the U. S. Geological - Survey] - - -Plate 58 - - [Illustration: Breccia] - - [Illustration: Conglomerate] - - -Plate 59 - - [Illustration: Calcareous shale] - - [Illustration: Coquina] - - -Plate 60 - - [Illustration: Foramenifera from Chalk; enlarged about 25 diameters] - - [Illustration: Encrinal Limestone; fragments of the stems, arms and - body of Crinoids] - - -Plate 62 - - [Illustration: _A_ diatomaceous earth magnified 50 times] - - [Illustration: _B_ and _C_ two diatoms from the above enlarged 250 - times. After Gravelle, by the courtesy of Natural History] - - -Plate 63 - - [Illustration: A metamorphic rock, showing the contortion of layers - due to expansion under heat] - - -Plate 64 - - [Illustration: A conglomerate partly metamorphosed to a gneiss. Note - the flattened pebbles and the alternation of the intermediate - material to mica scales, etc.] - - [Illustration: A typical gneiss] - - -Plate 66 - - [Illustration: Phyllite] - - [Illustration: A white marble, with black streaks due to graphite] - - -Plate 68 - - [Illustration: Claystones, simple and compound] - - [Illustration: A line concretion, which on splitting disclosed a - fern leaf of the age of the coal measures] - - -Plate 69 - - [Illustration: A septeria from Seneca Lake, N. Y.] - - [Illustration: Pisolite] - - -Plate 70 - - [Illustration: A geode filled with quartz crystals] - - -Plate 71 - - [Illustration: A quartz pebble from the bed of a New England brook] - - [Illustration: A pebble of schist and granite from the foot of Mt. - Toby, Mass.] - - -Plate 72 - - [Illustration: An iron-nickel meteorite, of 23 lbs. which fell in - Claiborne Co., Tenn.] - - [Illustration: An etched slice of an iron meteorite which fell in - Reed City, Osceola Co., Mich.] - - -Plate 73 - - [Illustration: A stony meteorite, about natural size, which fell in - 1875, in Iowa Co., Iowa] - - - PUTNAM’S - NATURE FIELD BOOKS - Companion books to this one - - Mathews American Wild Flowers - American Trees and Shrubs - Wild Birds and Their Music - Durand Wild Flowers in Homes and Gardens - My Wild Flower Garden - Common Ferns - Lutz Insects - Loomis Rocks and Minerals - Eliot Birds of the Pacific Coast - Armstrong Western Wild Flowers - Alexander Birds of the Ocean - Anthony North American Mammals - Thomas Common Mushrooms - Sturgis Birds of the Panama Canal Zone - Miner Seashore Life - Breder Marine Fishes of the Atlantic Coast - Morgan Ponds and Streams - Longyear Rocky Mountain Trees and Shrubs - Olcott Field Book of the Skies - Putnam - Beebe The Shore Fishes of Bermuda - Tee-Van - Schrenkeisen Fresh-Water Fishes of North America North of - Mexico - - - - - Transcriber’s Notes - - -—Retained publication information from the printed edition: this eBook - is public-domain in the country of publication. - -—In the text versions only, text in italics is delimited by - _underscores_. - -—Silently corrected a few typos. - -—Reconstructed an image caption (Pisolite) on Plate 69. - -—Generated a cover image based on elements in the book. - - - - - - - -End of the Project Gutenberg EBook of Field Book of Common Rocks and Minerals, by -Frederic Brewster Loomis and Walter Everett Corbin - -*** END OF THIS PROJECT GUTENBERG EBOOK FIELD BOOK OF COMMON ROCKS *** - -***** This file should be named 55382-0.txt or 55382-0.zip ***** -This and all associated files of various formats will be found in: - http://www.gutenberg.org/5/5/3/8/55382/ - -Produced by Stephen Hutcheson, Dave Morgan and the Online -Distributed Proofreading Team at http://www.pgdp.net - -Updated editions will replace the previous one--the old editions will -be renamed. - -Creating the works from print editions not protected by U.S. copyright -law means that no one owns a United States copyright in these works, -so the Foundation (and you!) can copy and distribute it in the United -States without permission and without paying copyright -royalties. 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} -p.biblio { text-align:justify; margin-left:2em; text-indent:-2em; } - -dl.biblio dt { margin-top:.6em; margin-left:2em; text-indent:-2em; text-align:justify; clear:both; } -dl.biblio dt div { display:block; float:left; margin-left:-6em; width:6em; clear:both; } -dl.biblio dt.center { margin-left:0em; text-align:center; text-indent:0; } -dl.biblio dd { margin-top:.3em; margin-left:3em; text-align:justify; font-size:90%; } -.clear { clear:both; } -p.book { margin-left:2em; text-indent:-2em; } -p.review { margin-left:2em; text-indent:-2em; font-size:80%; } -p.pcap { margin-left:0em; text-indent:0; text-align:center; margin-top:0; font-weight:bold; } -p.pcapc { margin-left:4.7em; text-indent:0em; text-align:justify; } -span.pn { display:inline-block; width:4.7em; text-align:left; margin-left:0; text-indent:0; }</style> -</head> -<body> - - -<pre> - -The Project Gutenberg EBook of Field Book of Common Rocks and Minerals, by -Frederic Brewster Loomis and Walter Everett Corbin - -This eBook is for the use of anyone anywhere in the United States and most -other parts of the world at no cost and with almost no restrictions -whatsoever. You may copy it, give it away or re-use it under the terms of -the Project Gutenberg License included with this eBook or online at -www.gutenberg.org. If you are not located in the United States, you'll have -to check the laws of the country where you are located before using this ebook. - -Title: Field Book of Common Rocks and Minerals - For identifying the Rocks and Minerals of the United States - and interpreting their Origins and Meanings - -Author: Frederic Brewster Loomis - Walter Everett Corbin - -Release Date: August 18, 2017 [EBook #55382] - -Language: English - -Character set encoding: UTF-8 - -*** START OF THIS PROJECT GUTENBERG EBOOK FIELD BOOK OF COMMON ROCKS *** - - - - -Produced by Stephen Hutcheson, Dave Morgan and the Online -Distributed Proofreading Team at http://www.pgdp.net - - - - - - -</pre> - -<div id="cover" class="img"> -<img id="coverpage" src="images/cover.jpg" alt="Field Book of Common Rocks and Minerals" width="468" height="901" /> -</div> -<div class="box"> -<h1>Field Book <i>of</i> -<br />Common Rocks -<br /><i>and</i> Minerals</h1> -<hr /> -<p class="center"><b>For identifying the Rocks and Minerals of the United States and interpreting their Origins and Meanings</b></p> -<hr /> -<p class="center">By -<br /><span class="large"><b>Frederic Brewster Loomis</b></span> -<br /><span class="small">Late Professor of Mineralogy and Geology -<br />in Amherst College</span></p> -<p class="tbcenter"><span class="small">With 47 Colored Specimens and over 100 other Illustrations from Photographs by W. E. Corbin and drawings by the Author</span></p> -<p class="tbcenter"><b><span class="large">G. P. Putnam’s Sons</span> -<br />New York and London</b></p> -</div> -<p class="center small">FIELD BOOK -<br />OF -<br />COMMON ROCKS AND MINERALS</p> -<p class="center small">Copyright, 1923, 1948 -<br />by -<br />Frederick Brewster Loomis</p> -<p class="center small">Twenty-sixth Impression -<br />Revised 1948</p> -<p class="center small">All rights reserved. This book, or parts thereof, must not be reproduced in any form without permission.</p> -<p class="center small">Made in the United States of America</p> -<p class="tbcenter"><span class="sc">Dedicated</span> -<br /><span class="small">TO</span> -<br /><span class="large">MY MOTHER</span> -<br /><span class="small">WHO ENCOURAGED ME WHILE A BOY TO GATHER MINERALS, ROCKS AND FOSSILS.</span></p> -<div class="pb" id="Page_vii">vii</div> -<h2 id="c1"><span class="h2line1">PREFACE</span></h2> -<p>Everyone, who is alert as he wanders about -this world, wants to know what he is seeing -and what it is all about. Here and there with -the aid of capable guides a few have been introduced -into the sphere of that wide and fascinating -knowledge of Nature which has been so rapidly -accumulated during this and the latter part of -the last century. It is a full treasure house -constantly being enriched, but unfortunately the -few who have been initiated have soon acquired -a technical language and habit, so that their -knowledge and new acquisitions are communicated -to but few. The public at large, not having -the language nor an interpreter at hand, has -come almost at once to a barrier which few have -the time or patience to surmount.</p> -<p>Latterly it has become clear that the largest -progress cannot be made if the knowledge of -any branch of Science is confined to a few only. -The most rapid advances have been made where -many men are interested and enthusiastic. In -no science should there be a difficult barrier -between the amateur and the professional student. -All Nature is equally open for everyone -to study, and there should never be created obstacles -as by the use of terminology not easily -acquired by anyone. Of late these barriers have -<span class="pb" id="Page_viii">viii</span> -been in part broken down and competent students -have written guides which anyone can -follow, and soon begin to know the plants, trees, -birds, insects, etc. So far no one has attempted -to make the study of minerals and rocks so direct -and simple that everyone can get a start. Most -books on minerals, and practically all those on -rocks are written for school courses, and to say -the least chill any enthusiasm which is naturally -aroused by the finding of interesting looking -rocks or minerals.</p> -<p>The purpose of this book is first of all to provide -a means of identifying minerals and rocks by -such methods as are practical without elaborate -equipment or previous training: and second to -suggest the conditions under which the various -minerals and rocks were formed, so that, at the -first contact, one may get a conception of the -events which have anteceded the mineral or -rock which has been found. For this purpose -keys have been worked out for determining the -rocks and minerals by such obvious features as -color, hardness, etc. Each mineral or rock is -introduced by a summary of its characters, then -the features by which it may be distinguished -from any other similar mineral are given, after -which its mode of origin and its meanings are -considered. For those interested in the composition -of the minerals, it is given in chemical -symbols with each mineral. Most classifications -of minerals are based on the composition, all the -sulphides, carbonates, etc., being grouped together, -but in this book, because the popular -interest and commercial uses are primarily in -<span class="pb" id="Page_ix">ix</span> -the metal present, the minerals are grouped in -each case about the chief metal, all the minerals -of iron being grouped together, for instance.</p> -<p>A few minerals and rocks which are not strictly -common have been included such as gems and -meteorites; the gems because they are of intense -interest to their owners and are often simply -perfect examples of a fairly common mineral; -and such forms as meteorites because it is important -that, if one should run across one, it should -be recognized, and so not lost to the world.</p> -<p>The book is freely illustrated, those minerals -in which color is important for identification -being illustrated in colors, and those which are -black, or in which the color is not a determining -factor, are shown in either photographic or -outline figures.</p> -<p>In the introductory chapter there are explanations -of the terms used in describing minerals, -and of the systems in which they are grouped. -A knowledge of the systems may not be a -necessity, but it is a great help in determining -minerals, and is very important in understanding -why the individual minerals take the varied -forms which are characteristic of them. These -systems will be better understood after a few -minerals have been gathered and examined.</p> -<p>It is hoped the book will help those who have -already some knowledge of rocks and minerals, -and especially that it will tempt many to begin -an acquaintance with the rocks and minerals -which are all about them, and are the foundation -on which our material progress is built. Rocks -and minerals have some advantages over most -<span class="pb" id="Page_x">x</span> -objects which are collected in that they neither -require special preparation before they can be -kept, nor do they deteriorate with time.</p> -<p>The author will appreciate corrections or -suggestions as to better presentation of the -material in this book.</p> -<p><span class="lr">F. B. L.</span></p> -<p><span class="sc">Amherst, Mass.</span></p> -<div class="pb" id="Page_xi">xi</div> -<h2 class="center">CONTENTS</h2> -<dl class="toc"> -<dt><span class="small">PAGE</span></dt> -<dt><a href="#c1"><span class="sc">Preface</span></a> vii</dt> -<dt class="jl"><span class="small">CHAPTER</span></dt> -<dt><a href="#c2"><span class="cn">I.—</span><span class="sc">An Introduction</span></a> 3</dt> -<dt><a href="#c3"><span class="cn">II.—</span><span class="sc">On the Forms and Properties of Minerals</span></a> 10</dt> -<dt><a href="#c4"><span class="cn">III.—</span><span class="sc">The Minerals</span></a> 25</dt> -<dt><a href="#c5"><span class="cn">IV.—</span><span class="sc">The Rocks</span></a> 170</dt> -<dt><a href="#c6"><span class="cn">V.—</span><span class="sc">Miscellaneous Rocks</span></a> 248</dt> -<dt><a href="#c7"><span class="cn"> </span><span class="sc">Bibliography</span></a> 270</dt> -<dt><a href="#c8"><span class="cn"> </span><span class="sc">Index</span></a> 273</dt> -</dl> -<div class="pb" id="Page_xiii">xiii</div> -<h2><span class="h2line1">LIST OF PLATES</span> -<br /><span class="h2line2">(AT END OF BOOK)</span></h2> -<dl class="toc"> -<dt><span class="small">PAGE</span></dt> -<dt><a href="#Plate_Frontispiece">Tourmaline crystals, growing amid feldspar crystals in a cavity in granite, from Paris, Me.</a> 279</dt> -<dt><a href="#Plate_1"><span class="sc">Plate</span> 1.—Basal forms of the isometric system</a> 311</dt> -<dt><a href="#Plate_2"><span class="sc">Plate</span> 2.—Basal forms of the tetragonal system. Basal forms of the orthorhombic system</a> 312</dt> -<dt><a href="#Plate_3"><span class="sc">Plate</span> 3.—Basal forms of the monoclinic system. A cross section of the prism with its edges beveled so that a six-sided prism is formed (pseudo-hexagonal). Basal form of the triclinic system.</a> 313</dt> -<dt><a href="#Plate_4"><span class="sc">Plate</span> 4.—Basal forms of the hexagonal system</a> 314</dt> -<dt><a href="#Plate_5"><span class="sc">Plate</span> 5.—Gold in quartz from California (<i>in color</i>)</a> 280</dt> -<dt><a href="#Plate_6"><span class="sc">Plate</span> 6.—Native silver in calcite. Argentite, the black masses throughout the white quartz (<i>in color</i>)</a> 281</dt> -<dt><a href="#Plate_7"><span class="sc">Plate</span> 7.—Pyrargyrite as it appears after moderate exposure to the light; streak at left. Crystal form of pyrargyrite. Prousite as it appears after moderate exposure to the light; streak at left (<i>in color</i>)</a> 282</dt> -<dt><a href="#Plate_8"><span class="sc">Plate</span> 8.—Native copper from Michigan. Chalcopyrite in tetrahedrons and an occasional octahedron; streak to the left (<i>in color</i>)</a> 283</dt> -<dt><a href="#Plate_9"><span class="sc">Plate</span> 9.—Chalcocite crystals with the bluish tarnish. Tetrahedrite crystals; streak to left (<i>in color</i>)</a> 284</dt> -<dt><a href="#Plate_10"><span class="sc">Plate</span> 10.—Tetrahedrons showing characteristic manner in which tetrahedrite occurs. A cube with the edges beveled and the corners cut in a form characteristic of cuprite</a> 315</dt> -<dt><a href="#Plate_11"><span class="sc">Plate</span> 11.—Cuprite, the red crystals showing characteristic color, others showing the green tarnish of malachite. Malachite (green) and azurite (blue), the two minerals shown together as they very commonly occur (<i>in color</i>)</a> 285</dt> -<dt><a href="#Plate_12"><span class="sc">Plate</span> 12.—Limonite. The crystal form in which goethite is found (<i>in color</i>)</a> 286</dt> -<dt><a href="#Plate_13"><span class="sc">Plate</span> 13.—Hematite. Clinton iron ore, oolitic. Siderite crystals (<i>in color</i>)</a> 287</dt> -<dt><a href="#Plate_14"><span class="sc">Plate</span> 14.—Crystal forms of hematite. A typical crystal of magnetite. The rhombohedron typical of siderite</a> 317</dt> -<dt><a href="#Plate_15"><span class="sc">Plate</span> 15.—Pyrite crystals. Marcasite in concretionary form with radiate structure (<i>in color</i>)</a> 288</dt> -<dt><a href="#Plate_16"><span class="sc">Plate</span> 16.—The pyritohedron. The pyritohedron with certain of its edges beveled by the cube faces, to show the relationship of these two forms</a> 318</dt> -<dt><a href="#Plate_17"><span class="sc">Plate</span> 17.—Galena in crystals. Pyromorphite crystals (Green) (<i>in color</i>)</a> 289</dt> -<dt><a href="#Plate_18"><span class="sc">Plate</span> 18.—Typical forms for cerrusite. Forms in which anglesite occurs</a> 319</dt> -<dt><a href="#Plate_19"><span class="sc">Plate</span> 19.—Sphalerite, some the normal yellow and some crystals with the reddish tinge. (White is dolomite.) Zincite, streak to the left (<i>in color</i>)</a> 290</dt> -<dt><a href="#Plate_20"><span class="sc">Plate</span> 20.—A characteristic form in which sphalerite may occur. Characteristic form for zincite crystals. Typical form of crystal of willemite</a> 320</dt> -<dt><a href="#Plate_21"><span class="sc">Plate</span> 21.—Smithsonite in yellow crystals. Franklinite in octahedral crystals, streak to left (<i>in color</i>)</a> 291</dt> -<dt><a href="#Plate_22"><span class="sc">Plate</span> 22.—Moss agates, showing the dendritic growth of manganitic minerals, like manganite or pyrolusite. Crystal form of manganite</a> 321</dt> -<dt><a href="#Plate_23"><span class="sc">Plate</span> 23.—Crystals of green corundum in syenite, from Montana. Typical crystal forms of corundum</a> 322</dt> -<dt><a href="#Plate_24"><span class="sc">Plate</span> 24.—Arsenopyrite, showing crystals massed so as to be incompletely developed. Realgar as it usually occurs in powdery incrustations (<i>in color</i>)</a> 292</dt> -<dt><a href="#Plate_25"><span class="sc">Plate</span> 25.—Large crystals of stibnite; the light colored face is the one parallel to which cleavage occurs. Niccolite is a vein in slate (<i>in color</i>)</a> 293</dt> -<dt><a href="#Plate_26"><span class="sc">Plate</span> 26.—Cobaltite, silver color, with pink tinge. Smaltite, pink is cobalt bloom (<i>in color</i>)</a> 294</dt> -<dt><a href="#Plate_27"><span class="sc">Plate</span> 27.—Carnotite from Southwest Colorado. Cinnabar (<i>in color</i>)</a> 295</dt> -<dt><a href="#Plate_28"><span class="sc">Plate</span> 28.—Cassiterite, twinned crystals. The crystal form in which both cassiterite and rutile occur when in simple crystals. Multiple twinning characteristic of rutile</a> 323</dt> -<dt><a href="#Plate_29"><span class="sc">Plate</span> 29.—Crystal of spinel. Crystal forms in which dolomite occurs</a> 324</dt> -<dt><a href="#Plate_30"><span class="sc">Plate</span> 30.—Two intergrowing or twinned quartz crystals. Diagram of the typical quartz crystal. A quartz crystal on which the left hand rhombohedron is represented by small faces, while the right hand rhombohedron has large faces</a> 316</dt> -<dt><a href="#Plate_31"><span class="sc">Plate</span> 31.—Amethyst, not however deep enough colored for gems. Jasper, with botryoidal surface (<i>in color</i>)</a> 296</dt> -<dt><a href="#Plate_32"><span class="sc">Plate</span> 32.—Banded agate from Brazil (<i>in color</i>)</a> 297</dt> -<dt><a href="#Plate_33"><span class="sc">Plate</span> 33.—Common opal from Arizona. Siliceous sinter or geyserite from Yellowstone Park (<i>in color</i>)</a> 298</dt> -<dt><a href="#Plate_34"><span class="sc">Plate</span> 34.—Orthoclase, a cleavage piece. Crystal forms of orthoclase. Diagram of a multiple twin of a plagioclase feldspar</a> 325</dt> -<dt><a href="#Plate_35"><span class="sc">Plate</span> 35.—A group of microcline crystals from Pike’s Peak, Colo. Labradorite, showing multiple twinning (the striation) and the iridescent play of colors (<i>in color</i>)</a> 299</dt> -<dt><a href="#Plate_36"><span class="sc">Plate</span> 36.—Crystal form of a pyroxene. Cross sections of a pyroxene crystal showing the lines of intersection of two cleavage planes. Cross sections of pyroxenes, showing typical forms taken by crystals. Augite crystals, in crystalline limestone (<i>in color</i>)</a> 300</dt> -<dt><a href="#Plate_37"><span class="sc">Plate</span> 37.—Diagrams of amphibole crystals. Tremolite in silky fibrous crystals, asbestos. Hornblende crystals in quartzite</a> 326</dt> -<dt><a href="#Plate_38"><span class="sc">Plate</span> 38.—The dodecahedron and the 24-sided figure characteristic of garnets. The garnet, grossularite. The garnet, alamandite (<i>in color</i>)</a> 301</dt> -<dt><a href="#Plate_39"><span class="sc">Plate</span> 39.—Beryl of gem quality. Zircon in syenite (<i>in color</i>)</a> 302</dt> -<dt><a href="#Plate_40"><span class="sc">Plate</span> 40.—Cyanite crystals in schist. A crystal of mica, showing basal cleavage (<i>in color</i>)</a> 303</dt> -<dt><a href="#Plate_41"><span class="sc">Plate</span> 41.—Crystal form typical of topaz. A topaz crystal from Brazil. Crystal form typical of staurolite when simple. A typical twin of staurolite (<i>in color</i>)</a> 304</dt> -<dt><a href="#Plate_42"><span class="sc">Plate</span> 42.—Epidote crystals. Typical forms of epidote crystals. Typical forms of tourmaline</a> 327</dt> -<dt><a href="#Plate_43"><span class="sc">Plate</span> 43.—Serpentine. Chlorite (<i>in color</i>)</a> 305</dt> -<dt><a href="#Plate_44"><span class="sc">Plate</span> 44.—The typical form of analcite. A typical natrolite crystal. The typical crystal form of stilbite. A sheaf-like bundle of fibrous crystals, typical of stilbite</a> 329</dt> -<dt><a href="#Plate_45"><span class="sc">Plate</span> 45.—A group of calcite crystals. Typical forms of calcite</a> 330</dt> -<dt><a href="#Plate_46"><span class="sc">Plate</span> 46.—Typical forms of aragonite. Typical form of the anhydrite crystal</a> 331</dt> -<dt><a href="#Plate_47"><span class="sc">Plate</span> 47.—A piece of gypsum looking on the surface of the perfect cleavage, and showing the two other cleavages as lines, intersecting at 66°. Twinning is also shown. A simple crystal of gypsum. Twin crystals of gypsum.</a> 332</dt> -<dt><a href="#Plate_48"><span class="sc">Plate</span> 48.—A group of barite crystals. Outline of the typical tabular barite crystal. The six-sided double pyramid, composed of three interpenetrating crystals, typical of witherite and strontianite</a> 328</dt> -<dt><a href="#Plate_49"><span class="sc">Plate</span> 49.—Apatite crystals in crystalline calcite. The ends of apatite crystals showing common modes of termination (<i>in color</i>)</a> 306</dt> -<dt><a href="#Plate_50"><span class="sc">Plate</span> 50.—A group of fluorite crystals. A group of halite crystals (<i>in color</i>)</a> 307</dt> -<dt><a href="#Plate_51"><span class="sc">Plate</span> 51.—Sulphur crystals. Ice crystals, the top one, the end of a hexagonal prism; the two lower figures multiple twins as in snow flakes</a> 333</dt> -<dt><a href="#Plate_52"><span class="sc">Plate</span> 52.—The Devil’s Tower, Wyoming, an example of igneous rock with columnar structure, and resting on sedimentary rocks</a> 334</dt> -<dd>Courtesy of the U. S. Geological Survey</dd> -<dt><a href="#Plate_53"><span class="sc">Plate</span> 53.—A coarse granite. Graphic granite</a> 335</dt> -<dt><a href="#Plate_54"><span class="sc">Plate</span> 54.—Syenite. Gabbro</a> 336</dt> -<dt><a href="#Plate_55"><span class="sc">Plate</span> 55.—Basalt-porphyry. The large white crystals are phenocrysts of plagioclase feldspar. Basalt-obsidian</a> 337</dt> -<dt><a href="#Plate_56"><span class="sc">Plate</span> 56.—Amgydoloid</a> 338</dt> -<dt><a href="#Plate_57"><span class="sc">Plate</span> 57.—The north face of Scott’s Bluff, Neb., showing sedimentary sandstones above and clays below. The type of erosion is characteristic of arid regions</a> 339</dt> -<dd>Courtesy of the U. S. Geological Survey</dd> -<dt><a href="#Plate_58"><span class="sc">Plate</span> 58.—Breccia. Conglomerate</a> 340</dt> -<dt><a href="#Plate_59"><span class="sc">Plate</span> 59.—Calcareous shale. Coquina</a> 341</dt> -<dt><a href="#Plate_60"><span class="sc">Plate</span> 60.—Foramenifera from chalk; enlarged about 25 diameters. Encrinal limestone; fragments of the stems, arms and body of crinoids</a> 342</dt> -<dt><a href="#Plate_61"><span class="sc">Plate</span> 61.—Amber. Two bottles of petroleum, the left hand one with a paraffin base, the right hand one with an asphalt base (<i>in color</i>)</a> 308</dt> -<dt><a href="#Plate_62"><span class="sc">Plate</span> 62.—Diatomaceous earth magnified 50 times. Two diatoms from the above enlarged 250 times</a> 343</dt> -<dd>After Gravelle, by the courtesy of Natural History</dd> -<dt><a href="#Plate_63"><span class="sc">Plate</span> 63.—A metamorphic rock, showing the contortion of layers due to expansion under heat</a> 344</dt> -<dt><a href="#Plate_64"><span class="sc">Plate</span> 64.—A conglomerate partly metamorphosed to a gneiss. A typical gneiss</a> 345</dt> -<dt><a href="#Plate_65"><span class="sc">Plate</span> 65.—Mica schist, with garnets. Chlorite schist (<i>in color</i>)</a> 309</dt> -<dt><a href="#Plate_66"><span class="sc">Plate</span> 66.—Phyllite. A white marble, with black streaks due to graphite</a> 346</dt> -<dt><a href="#Plate_67"><span class="sc">Plate</span> 67.—Serpentine composed of serpentite, hematite, and some calcite (<i>in color</i>)</a> 310</dt> -<dt><a href="#Plate_68"><span class="sc">Plate</span> 68.—Claystones, simple and compound. A lime concretion, which on splitting disclosed a fern leaf of the age of the coal measures</a> 347</dt> -<dt><a href="#Plate_69"><span class="sc">Plate</span> 69.—A septeria from Seneca Lake, N. Y. Pisolite from Nevada</a> 348</dt> -<dt><a href="#Plate_70"><span class="sc">Plate</span> 70.—A geode filled with quartz crystals</a> 349</dt> -<dt><a href="#Plate_71"><span class="sc">Plate</span> 71.—A quartz pebble from the bed of a New England brook. A pebble of schist and granite from the foot of Mt. Toby, Mass.</a> 350</dt> -<dt><a href="#Plate_72"><span class="sc">Plate</span> 72.—An iron-nickel meteorite, of 23 lbs., which fell in Claiborne Co., Tenn. An etched slice of an iron meteorite which fell in Reed City, Osceola, Co., Mich.</a> 351</dt> -<dt><a href="#Plate_73"><span class="sc">Plate</span> 73.—A stone meteor, about natural size, which fell in 1875 in Iowa Co., Iowa</a> 352</dt> -</dl> -<div class="pb" id="Page_xix">xix</div> -<h1 title="">FIELD BOOK OF -<br />COMMON ROCKS AND MINERALS</h1> -<div class="pb" id="Page_3">3</div> -<h2 id="c2"><span class="h2line1">CHAPTER I</span> -<br /><span class="h2line2">AN INTRODUCTION</span></h2> -<h3>Why</h3> -<p>Why should one be interested in -rocks and minerals? Because the -whole world is made of rocks and minerals. -They are the foundations on which we build. -From them we draw all our metals, and the -extent to which we utilize our minerals is a -measure of the advance of our civilization. Fragments -of rock are the soil from which, by way -of the plants, we draw our food, and ultimately -our life. The rocks make wild or gentle scenery, -one at least of the sources of pleasure. Knowledge -of rocks and minerals is then knowledge of -fundamentals, of ultimate sources. Between -finding the raw materials and their present uses -there are usually many steps (so many that we -forget that the beginning and end are united), -as for instance in your watch. It is made of gold, -brass, steel, agate, glass, and perhaps has luminous -radium paint on the hands. It is a long way -from finding and mining gold, chalcopyrite, -hematite, carnotite, etc., through the raw materials, -gold, copper, iron, etc., to the finished -watch, but the minerals are the foundations of -the watch; and it took centuries to find them and -learn one by one how to use them, from the gold -<span class="pb" id="Page_4">4</span> -10,000 years ago down to the radium within the -last fifty years. Then too there is joy in going -out into Nature’s wild and raw places, joy in -being on the foundations of the earth, joy in the -scenery, in the beauty of the minerals themselves.</p> -<p>But why collect the rocks and minerals? First -because this is the way to know them. Both -mineral and rocks require careful examination -in order to see all those fine points by which they -are distinguished. It is often necessary to -compare one with another to get in mind the -differences of form, color, streak, though with -increasing familiarity these characteristics are -recognized at first sight. It is the repeated -examination which makes a rock tell the story -of the country from which it came. Our first -attempts to read the story give us only the most -general facts. Nature’s book, written in the -rocks, has to be read closely, often between the -lines. Until we are used to the characters in -which the words are written, we read slowly. -When they look at Nature’s book, always open, -most people do not read; for they do not know -their letters. Every mineral is a letter, every -rock a word, and we learn to read as we learn the -minerals and rocks, and every time we go over -them we get more facts coming out. The place -where a rock or mineral occurs is of course the -relation between them, and is involved in reading -the story. No one today is a perfect reader. -We are all learning to see more in the rocks day -by day. So it is important to have the rocks -and minerals where they can be handled and -<span class="pb" id="Page_5">5</span> -repeatedly examined, where we can turn to them -in our leisure moments. Don’t stop when you -have learned the name of a mineral or rock. -You need more. See what it means. Secondly, -minerals have beauties of form, color, and structure, -and they do not fade. They will be as -perfect in ten years as when found. We are all -naturally crows, and love to gather the objects -which interest us. It is not a bad habit, and only -needs directing. Cultivate it. Have a hobby, -and minerals and rocks are a good one; for they -are like treasures in Heaven which “neither moth -nor rust doth corrupt.” Not only will they give -you pleasure, but they will be a constructive -education, training the eye to see, and the mind -to think straight. No one ever regretted the -time and effort spent in collecting either minerals -or rocks.</p> -<h3>Collecting</h3> -<p>In order to make a collection valuable -two or three rules must be observed. -In the case of rocks, collect large enough -samples so that they will be characteristic, and -clear in their make-up. The standard size for -rocks is 3 × 4 inches on top and one to two inches -thick according to the nature of the rock. Tiny -fragments do not give the character of the rock -as well, and they are all the time getting into -confusion. <b>Every specimen should be labeled</b>, -with at least its name and the exact locality from -which it came. Composition, structural features, -associations, and classification may be added, the -more the better; for each item adds to the information -and interest of the specimen. One may -<span class="pb" id="Page_6">6</span> -make his own labels or have printed blanks, -and may put as much care and art into the -labels as desired, the more the better. One thing -is very important and that is to have a number -on the label with a corresponding one on the -specimen, so that in case they should get separated, -they may be readily brought together, -even by one who is not familiar with the individual -specimens. Lastly, give your collection -as good a place as possible, either in drawers, -boxes or in a case. The specimens are worth -being kept in order and where they can be readily -seen and compared. Nature is systematic, and -there is a reason for the order in which rocks and -minerals are taken up. It is desirable either that -this order, or some one of the orders of Nature -appear in the collection. In this book the metals -are the basis of classification, all those minerals -primarily related to one of the metals being -grouped together.</p> -<p>In collecting minerals, the size of the specimens -can not be so regularly followed, but it -should be followed when collecting non-crystalline -minerals, and when possible. Crystals -however are chosen from a variety of points of -view, as perfection of form, color, examples of -cleavage, twinning, etc.; so that in many cases -smaller or larger examples must appear in the -collection. It is always desirable that as many -variations of a rock or mineral as possible should -appear in the collection, and in many cases -examples of the matrix from which the crystals -came. When crystals are tiny, it is well to place -them in vials, that they may not be lost.</p> -<div class="pb" id="Page_7">7</div> -<h3>Where</h3> -<p>Where shall we start in making a -collection? Near home. Get the -local minerals and rocks first, and then range as -widely as possible. The best places are bare and -exposed rocks, especially where fresh and un-weathered -surfaces are available. Quarries and -where there has been blasting along roads offer -fine opportunities. Fissures and cavities in the -rocks are especially likely to have fine crystals, -and in all localities continued search will reveal -a surprising number of different minerals. The -greatest variety occur in metamorphic rocks, or -where igneous rocks come in contact with other -rocks, but even the sedimentary rocks have a -goodly range of minerals. All through the -glaciated regions of the northern United States -lie scattered boulders brought from afar, which -will yield a surprising number of minerals and -variety of rocks.</p> -<h3>Equipment</h3> -<p>One may start with a very simple -equipment, a geologist’s or stone -mason’s hammer which can be obtained at any -hardware store, being sufficient for field work. -Rocks should be broken, so as to show fresh -surfaces and to get below the disintegrating -effects of weathering. At home one should have -a streak plate (a piece of unglazed porcelain), a -set of hardness minerals (see <a href="#Page_20">page 20</a>), and a -small bottle each of hydrochloric and nitric acid. -A pocket lens is useful in order to see more clearly -the form of small minerals. These things can be -purchased of any Naturalist’s Supply Co., like -Ward’s Natural Science Establishment, P.O. 24, -<span class="pb" id="Page_8">8</span> -Beachwood Sta., Rochester, N. Y., or the Kny-Scheerer -Corp., 483 First Ave., New York City. -Success depends upon a quick eye, and persistent -hunting. When traveling, opportunities -are offered at frequent intervals to see and get -new specimens.</p> -<h3>Study Your Collection</h3> -<p>Be sure and see the meaning in -each rock and mineral. The history -of the country is revealed in its -rocks and minerals. Note whether the rocks are -horizontal or folded, whether they change character -from place to place, or vertically. In going -over a piece of country you may locate an ancient -mountain system now leveled, by noting a -series of metamorphic rocks, with a central core -of granite, the roots of former mountains. Don’t -be afraid to draw conclusions from what you see. -Later, when the opportunity offers, look up the -region in the geological folio, bulletin, or map of -that section, and check up your findings. These -geological folios and bulletins, of which there is -one for nearly every region, are a great help to -collectors in suggesting where to look for various -rocks and minerals. Write to the Director of -the U. S. Geological Survey, Washington, D. C., -for a catalogue of the publications of the United -States Survey, or find out from him what are the -maps or folios for the region in which you are -interested. These U. S. publications cost but -little. When opportunity presents itself, visit -other collections. In them you will see some of -the minerals or rocks which have puzzled you, -and there is nothing quite so satisfactory as -<span class="pb" id="Page_9">9</span> -seeing the rocks or minerals themselves. No -description can always be so convincing. Then -too you will get suggestions as to localities that -you can visit.</p> -<h3>Literature</h3> -<p>As your collection grows, if you -find you have special interest in one -or another branch of the field, you can get books -giving more details in that line; and at the back -of this book will be found a list of such books.</p> -<div class="pb" id="Page_10">10</div> -<h2 id="c3"><span class="h2line1">CHAPTER II</span> -<br /><span class="h2line2">ON THE FORMS AND PROPERTIES OF MINERALS</span></h2> -<h3>Rocks</h3> -<p>All we know of the earth by direct -observation is confined to less than -four miles depth; though by projecting downward -the layers of rock that come to the surface, we -may fairly assume a knowledge of the structure -down to six or eight miles depth. This outer -portion is often referred to as the “crust of the -earth,” but the idea that the deeper portions are -molten is no longer held. This outer portion is -made of rocks, and a rock may be defined as, <i>a -mass of material, loose or solid, which makes up an -integral part of the earth</i>, as granite, limestone, or -sand. The rocks (except glassy igneous ones) -are aggregates of one or more minerals; either in -their original form like the quartz, feldspar and -mica of granite, or in a secondary grouping, -resulting from the units having been dislodged -from their primary position and regrouped a -second time, as in sandstone or clay.</p> -<h3>Minerals</h3> -<p>Since the rocks are aggregates of -minerals, it is best to take up the -minerals first. A mineral may be defined as <i>a -natural inorganic substance of definite chemical -composition</i>. It is usually solid, generally has -<span class="pb" id="Page_11">11</span> -crystalline structure, and may or may not be -bounded by crystal faces. <i>A crystal is a mineral, -bounded by symmetrically grouped faces, which -have definite relationships to a set of imaginary -lines called axes.</i> There are between 1100 and -1200 minerals, of which 30 are so frequently -present, and so dominant in making up the rocks, -that they are termed <i>rock-forming minerals</i>. -About 150 more occur frequently enough so that -they can be termed common minerals, and one -may expect to find a fairly large proportion of -them. Some of these are abundant in one part -of the country and rare in others, but this book is -written to cover the United States, and so all -those which have a fair abundance are included, -though some will only be found in the west and -others mostly in the east. Then there are some -more minerals which are really rare, but which -are cherished because of their beauty of color, -and are used as gems. These are mentioned, and -many of the gems are simply clear and beautiful -examples of minerals, which in dark or cloudy -forms are much more common. If one finds any -of these rare minerals which are not mentioned -in this book, he must turn to one of the larger -mineralogies mentioned in the literature list to -determine them.</p> -<h3>Crystal Structure</h3> -<p>A crystal is a mass of molecules, -all of the same composition. A molecule -in its turn is made up of atoms, -and each atom is a unit mass of an element. -Thus the calcite molecule is made up of one -unit or atom of calcium, one of carbon, and three -<span class="pb" id="Page_12">12</span> -of oxygen (CaCO₃). These atoms are held together -by an attraction, and make a molecule, -and for the study of minerals the molecule is the -unit. The mineral, calcite, is a mass of molecules -all like the one above, and each molecule -so small as to be invisible even with the aid of the -most powerful microscope. When calcite is in -crystal form, the molecules, like ranks of soldiers, -are arranged each in its place, each at a definite -distance from the other. While each molecule -may vibrate or wiggle within certain limits it -does not leave its place. (The comparison with -soldiers is a good one for the molecules of one -layer, but it must be remembered that in a -crystal there are also like spacings and ranks up -and down as well.) As long as the molecules -remain in fixed ranks, up and down, forward and -back, and sideways, the crystal is perfect. Calcite -may be heated until it melts and becomes -liquid. Then the molecules leave their definite -arrangement and move about in all sorts of directions, -like the soldiers after ranks have broken. -So long as the molecules are thus free to move -about but keep together, the substance is a -liquid. There are cases when the molecules in -this disorder take fixed positions without falling -into ranks. Such minerals are non-crystalline -and usually appear glassy. If still greater heat -is applied to the mineral in liquid form, a point -is reached (the vapor point), above which the -molecules go flying away from each (like soldiers -in a panic), each seeking to get as far from the -other as possible, so only a container will prevent -their dissipation. When in this condition a -<span class="pb" id="Page_13">13</span> -mineral is gaseous. When cooled, the reverse -order obtains. The molecules of gas gather into -a miscellaneous mob or liquid: and if this is -further cooled (but not too suddenly), they fall -into ranks and make a crystal. This may be -illustrated with water. When above 212° F. it is -steam (molecules wildly dissipated); when between -212° and 32° it is water (molecules close -to each other, but milling like a herd of cattle); -and when below 32° it is ice, the molecules ranged -in perfect order, rank on rank.</p> -<h3>Crystal Systems</h3> -<p>With all the possible forms that -crystals can and do take, there are -six systems of arrangement. First -there is the case where ranks, files, and vertical -rows are all equal, and now to be scientific, instead -of talking about ranks, files, etc., we use -the term axes to express these ideas; the files or -arrangements from front to back, being called -the <i>a axis</i>, the ranks, or side to side arrangement -the <i>b axis</i>, and the vertical arrangement -the <i>c axis</i>. (See <a href="#Plate_1">Plate 1</a>.) These axes are imaginary -lines, but they represent real forces.</p> -<h3>Isometric system</h3> -<p>When the axes are all equal and -at right angles to each other, a -crystal is said to be in the <b>isometric -system</b>. The cube is the basal form -and each side is known as a face. The ends -of the axes come to the middle of the cube -faces. The essential feature of this system is -that whatever happens to one axis must happen -to all, which is another way of saying that all -<span class="pb" id="Page_14">14</span> -the axes are equal. If we think of the cube as -having the corners cut off, we would have a new -face on each of the eight corners, in addition -to the six cube faces. Then if each of these -new faces were enlarged until they met and -obliterated the cube faces, an eight-sided figure, -the octahedron, would result. In this the axes -would ran to the corners. Another modification -of the cube would be to bevel each of its twelve -edges, making twelve new faces in addition to -the six cube faces. If we think of these new -faces being developed until they meet and -obliterate the cube faces, there will result a -twelve-sided figure, the dodecahedron. And -the 24 edges of the dodecahedron could be -beveled to make a 24-sided figure, and so on. -Of course in Nature the corners are not cut, nor -the edges beveled, but as a result of the interaction -of the forces expressed by the axes and -the distribution of the molecules, the molecules -arrange themselves in a cube, octahedron, dodecahedron -or combination of these basal forms.</p> -<h3>Crystal formation</h3> -<p>Crystals are formed in liquids as -they cool or evaporate and can no -longer hold the minerals in solution. -Crystals start about a center or nucleus, and -molecule by molecule, the orderly arrangement -is increased and the crystal grows, there being -no size which is characteristic. If free in the -liquid the crystal grows perfectly on all sides, but -if crystals are growing side by side, there comes a -time when they interfere with each other. Then -the free faces continue to grow and the orderly -<span class="pb" id="Page_15">15</span> -internal arrangement is maintained, though -externally there is interference.</p> -<h3>Tetragonal system</h3> -<p>In the second or <b>tetragonal system</b> -one axis (the c axis) is different from -the other two, but all three are still -at right angles with each other. This is saying -scientifically that the lines of force are greater -or less in one direction than in the other two, but -they act at right angles to each other. The a -and the b axes are equal and anything that -happens to one of these two must happen to the -other, but need not happen to the c axis. Thinking -of the molecules that arrange themselves -under this system of forces, it is clear that the -simplest form will be a square prism, <i>i.e.</i>, front -to back, and from side to side the numbers of -molecules will be equal, but up and down there -will be a greater or lesser number. If the eight -corners of this prism were cut, and these corner -faces increased in size until they met, the resulting -octahedron would be longer (or shorter) from -top to bottom than from side to side or front to -back, but the measurement from front to back -would be equal to the one from side to side. In -this system we may have the vertical edges of the -prism beveled, and not have to bevel the horizontal -ones, or we may bevel the horizontal edges -and not the vertical ones. There is no dodecahedron -in this system or in any other system -than the isometric. The forms in this tetrahedral -system are really a combination of the four -sides of the square prism with such modifications -as equally affect them all, with two ends which -<span class="pb" id="Page_16">16</span> -may be flat, or pyramidal, or modified pyramidal -faces.</p> -<h3>Orthorhombic system</h3> -<p>The third system has all three axes -unequal, but all three are still at -right angles with each other. This -is saying that the lines of force in the crystals -are all at right angles to each other but of unequal -value. The faces in this case are all in -pairs. What happens at one end of an axis -must happen at the opposite end, but does not -need to happen at the ends of any of the other -axes. We are dealing with pairs of faces (one -at either end of an axis), and if three such -pairs are combined in the simplest manner, the -resulting figure will be a rectangular prism. If -we cut the eight corners of this prism and enlarge -the faces until they meet, the result is -an octahedron, in which the distance from top -to bottom, from side to side, or from front to -back is not the same in any two cases. (See -<a href="#Plate_2">Plate 2</a>.) In this system if a face is made by -beveling one edge of the prism there must be a -corresponding face on the edge diagonally -opposite, but there does not have to be one on -any of the other edges. However if a corner is -cut, that face affects all the axes and so all the -corners must be cut. A great many crystals -occur in this system, and some of them which -are prismatic in shape may give trouble, for it is -not uncommon for the vertical edges of the prism -to be so beveled, that two of the original prism -faces are obliterated, and the two remaining faces -added to the four new faces make a six-sided -prism, which at first glance seems to belong to the -<span class="pb" id="Page_17">17</span> -hexagonal system. (See <a href="#Plate_3">Plate 3</a>, fig. 3.) Close -examination however will show that, instead of -all the prism faces being alike, as would be -necessary for the hexagonal system, they are -really in pairs, and one pair at least will be -distinguished in some way, such as being striated, -pitted, or duller.</p> -<h3>Monoclinic system</h3> -<p>The fourth system has all the axes -unequal, the a axis and the b axis -at right angles to each other, but -the c axis is inclined to the a axis, meeting it -at some other than a right angle. The <b>monoclinic -system</b> is like the orthorhombic system -except that it leans, or is askew, in one direction. -The result is that the faces at the ends -of the b axis are rhombohedral, while the others -are rectangular. As in the foregoing system, -the faces are in pairs at opposite ends of the -axes; and as in the orthorhombic system, a -face may occur on one edge and only have to -be repeated on the edge diagonally opposite. -The simplest form in this system will be made -by combining the three pairs of faces at the -opposite ends of the axes, which gives a prism, -which is rectangular in cross section, but leans -backward (or forward) if placed on end. As -in all the systems, if a corner is cut, all must -be cut; and if these corner faces are extended -to meet each other, an octahedron results, in -which, as in the prism, no two axes are equal. -If this octahedron is properly orientated (<i>i.e.</i> -with the a and b axes horizontal), it will lean -forward or backward. Many minerals belong to -<span class="pb" id="Page_18">18</span> -this system; and, as in the orthorhombic system, -it is not uncommon to have the vertical edges so -beveled that two of the prism faces are obliterated, -and the remaining two prism faces with -the four new faces make a six-sided prism, which -seems hexagonal. (See <a href="#Plate_3">plate 3</a>, figure 3.) However, -such a pseudo-hexagonal prism may be -recognized by at least one pair of the faces having -distinguishing marks (striæ, pits, or dullness), -instead of all being just alike.</p> -<h3>Triclinic system</h3> -<p>The fifth or <b>triclinic system</b> has -all the axes unequal, and no two of -them intersect at right angles. As -in the two preceding systems the faces occur -in pairs at the opposite ends of the axes. This -is the most difficult system in which to orientate -a crystal, but fortunately only a few crystals -occur in this system, such as the feldspars.</p> -<h3>Hexagonal system</h3> -<p>Lastly there is a group of crystals -which have four axes, one vertical, -and three in the horizontal plane -which intersect each other at angles of 60°, -all these three being equal to each other, but -different from the vertical axis. The simplest -form in this system is the six-sided prism. If -one corner of this prism is cut all must be, -and if these corner faces are extended to meet -each other, a double-six-sided pyramid results. -In this system if one of the vertical edges of -the prism is beveled, all must be, but the horizontal -edges need not be; or the horizontal edges -may be beveled and the vertical ones not. The -ends as they are related to the c axis may be -<span class="pb" id="Page_19">19</span> -developed independently of the prism, and so -the prism may be simply truncated by a flat end, -or have pyramids on either end.</p> -<h3>Hemihedral forms</h3> -<p>In this system it is quite common -to have forms which result from the -development of each alternate face of -either the prism or the double pyramid. In the -case of the prism, if every alternate face is developed -(and the others omitted) a three-sided -prism results, as in tourmaline. In the case of -the double pyramid if the three alternate faces -above are united with the three alternate faces -below, a six-sided figure is formed, which is -known as the rhombohedron, as all the faces are -rhombohedral in out-line and all equal. These -forms in which only half the faces are developed -are known as <b>hemihedral forms</b>. The same sort -of thing may happen in the isometric system in -the case of the octahedron, and also in the case -of the octahedron of other systems. When half -the faces of the octahedron are developed, two -above unite with two below and make a four-sided -figure, known as a tetrahedron. (See <a href="#Plate_10">plate 10</a>.) -While tetrahedrons may occur in any of -the first five systems they are not common outside -the isometric system.</p> -<h3>Twinning</h3> -<p>Another modification of the simple -forms which will be met occasionally -is <b>twinning</b>. By this is meant two crystals -growing together as though placed side by side -on some one of the faces, and then revolved until -the two axes which would normally be parallel -are at some definite angle with each other, 60°, or -<span class="pb" id="Page_20">20</span> -180° which is commoner. The surface of contact -between the two crystals is called the <i>composition -face</i>, and as no more material can be added on -that face the crystals continue to grow developing -the other faces, and we find faces in contact -with each other which should be at the opposite -end or other side of the crystals. This contact of -faces which should not come in contact, and the -presence of reentrant angles are indications of -twinning. In some minerals the twinning may -be repeated time and again, and if the twinning -is on one of the end faces a branching structure -results, as in frost and snow crystals, or the -multiple twinning may be of crystals growing -side by side when the final form will approximate -a series of thin sheets placed side by side as in -some feldspars. The peculiar forms characteristic -of individual minerals are taken up under -the respective minerals.</p> -<p>Other important properties of minerals are -hardness, cleavage, specific gravity, streak, luster, -and color.</p> -<h3>Hardness</h3> -<p><b>Hardness</b> may be defined as the -mineral’s resistance to abrasion or -scratching. It is measured by comparing a -mineral with Moh’s scale, a set of ten minerals -arranged in the order of increasing hardness, as -follows:</p> -<dl class="undent"><dt>1 <a href="#species_Talc">talc</a></dt> -<dt>2 <a href="#species_Gypsum">gypsum</a></dt> -<dt>3 <a href="#species_Calcite">calcite</a></dt> -<dt>4 <a href="#species_Fluorite">fluorite</a></dt> -<dt>5 <a href="#species_Apatite">apatite</a></dt> -<dt>6 <a href="#species_Feldspar">feldspar</a></dt> -<dt>7 <a href="#species_Quartz">quartz</a></dt> -<dt>8 <a href="#species_Topaz">topaz</a></dt> -<dt>9 <a href="#species_Corundum">corundum</a></dt> -<dt>10 <a href="#species_Diamond">diamond</a></dt></dl> -<div class="pb" id="Page_21">21</div> -<p>A set for measuring hardness may be purchased -from any dealer in mineral supplies. For rough -determination, as in the field, the following -objects have the hardness indicated; the finger -nail 2¼, a penny 3, a knife blade about 5.5, and -glass not over 6. In testing, a mineral is harder -than the one it will scratch, and softer than the -one by which it is scratched. For instance, if a -mineral will scratch calcite and is scratched by -fluorite, it is between 3 and 4 in hardness, say -3.5. When two samples mutually scratch each -other they are of equal hardness. Care must be -used in determining hardness, especially with the -harder minerals; for often, when testing a mineral, -the softer one will leave a streak of powder -on the harder one, which is not a scratch. One -should always rub the mark to make sure it is -really a groove made by scratching.</p> -<h3>Cleavage</h3> -<p><b>Cleavage</b> is the tendency, characteristic -of most minerals, and due -to the arrangement of their molecules, to cleave -or break along definite planes. The cleavage of -any mineral is not irregular or indefinite, but -characteristic for each mineral, and always -parallel to possible or actual faces on the crystal, -and always so described. For instance galena -has three cleavages, all equally good, and -parallel to the cube faces; so it is said to have -cubic cleavage. In the same way fluorite has -octahedral cleavage, and calcite rhombic cleavage. -In some minerals cleavage is well developed -in one plane, and less developed in other -planes, or it may be lacking altogether. The -<span class="pb" id="Page_22">22</span> -varying degrees of perfection by which a -mineral cleaves are expressed as, perfect -or imperfect, distinct or indistinct, good or -poor, etc.</p> -<h3>Specific gravity</h3> -<p>The <b>specific gravity</b> of a mineral -is its weight compared with the -weight of an equal volume of water, -and is therefore the expression of how many -times as heavy as water the mineral is. For -instance the specific gravity of pyrite is 5.1, -which is saying it is 5.1 times as heavy as -water. In a pure mineral the specific gravity -is constant, and an important factor in making -final determinations. As ordinarily obtained, -a piece of pure mineral is weighed in air, -which value may be called x. It is then immersed -in water and again weighed, and this -value is called y. The difference between the -weight in air and that in water is the weight -of an equal volume of water. Then we have -the following formula:</p> -<div class="center">specific gravity = <table class="inline"><tr><td>x</td></tr><tr><td class="ol">x-y</td></tr></table>.</div> -<p>Various balances have been devised for making -these measurements, but any balance which will -weigh small objects accurately, may be adapted -to specific gravity work, by hanging a small pan -under the regular weighing pan. When using -this balance, care is taken to see that the lower -pan is always submerged in water, even while -the mineral is being weighed in air, so that -when weighed in water in the lower pan, -the weight of this lower pan has already been -considered.</p> -<div class="pb" id="Page_23">23</div> -<h3>Streak</h3> -<p>By <b>streak</b> is meant the color of the -mineral when powdered. For some -minerals, especially metallic ores, it is of great -importance, for it remains constant, though the -color of the surface of the mineral changes -materially. It is most readily determined by -rubbing a corner of the mineral on a piece of -unglazed porcelain. Small plates, known as -“streak plates” are made for this purpose.</p> -<h3>Luster</h3> -<p>The <b>luster</b> of a mineral is the -appearance of its surface by reflected -light, and it is an important aid in determining -many minerals. Two types of luster are -recognized; metallic, the luster of metals, most -sulphides and some oxides, all of which are -opaque on their thin edges; and non-metallic, -the luster of minerals which are more or less -transparent on their thin edges, and most of -which are light colored. The common non-metallic -lusters are; vitreous, the luster of glass; -resinous, the appearance of resin; greasy, -oily appearance; pearly, the appearance of -mother-of-pearl; silky, like silk due to the -fibrous structure; adamantine, brilliant like a -diamond; and dull, as is chalk.</p> -<h3>Color</h3> -<p>When used with caution <b>color</b> is -of the utmost importance in determining -minerals, especially in making rapid -determinations. In metallic minerals it is constant -and dependable; but in the non-metallic -minerals it may vary, due to the presence of -small amounts of impurities which act as pigments. -<span class="pb" id="Page_24">24</span> -Color depends on chemical composition, -and when not influenced by impurities is termed -<i>natural</i>; but when the color is due to some inclosed -impurity it is termed <i>exotic</i>. In this latter -case caution must be used in making determinations. -Many minerals are primarily colorless, -but take on exotic colors as a result of the -presence of small quantities of impurities; for -instance, pure corundum is colorless, but with a -trace of iron oxide present becomes red, and is -called the ruby, or with a trace of cobalt becomes -blue and is called sapphire.</p> -<div class="pb" id="Page_25">25</div> -<h2 id="c4"><span class="h2line1">CHAPTER III</span> -<br /><span class="h2line2">THE MINERALS</span></h2> -<h4>KEY TO THE MINERALS, BASED ON HARDNESS, COLOR, ETC.</h4> -<table class="center" summary=""> -<tr class="th"><th colspan="5">OPAQUE COLORS</th></tr> -<tr class="th"><th><span class="sc">Color</span> </th><th><span class="sc">Hardness</span> </th><th><span class="sc">Streak</span> </th><th><span class="sc">Remarks</span> </th><th><span class="sc">Mineral</span></th></tr> -<tr><td class="l">Red</td></tr> -<tr><td class="l"><span class="hst">scarlet</span> </td><td class="l">2.5 </td><td class="l">scarlet </td><td class="l">surface tarnishes black </td><td class="l"><a href="#species_Prousite">prousite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">vermilion </td><td class="l">surface scarlet to dark red </td><td class="l"><a href="#species_Cinnabar">cinnabar</a></td></tr> -<tr><td class="l"><span class="hst">ochre</span> </td><td class="l">7 </td><td class="l">white </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Jasper">jasper</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">ochre red </td><td class="l">color red to almost black </td><td class="l"><a href="#species_Hematite">hematite</a></td></tr> -<tr><td class="l"><span class="hst">rose</span> </td><td class="l">4 </td><td class="l">white </td><td class="l">effervesces in warm acid </td><td class="l"><a href="#species_Rhodochrosite">rhodochrosite</a></td></tr> -<tr><td class="l"><span class="hst">dark</span> </td><td class="l">4 </td><td class="l">orange </td><td class="l"> </td><td class="l"><a href="#species_Zincite">zincite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">purplish red </td><td class="l">surface tarnishes black </td><td class="l"><a href="#species_Pyrargyrite">pyrargyrite</a></td></tr> -<tr><td class="l"><span class="hst">brownish</span> </td><td class="l">3.5 </td><td class="l">brownish red </td><td class="l"> </td><td class="l"><a href="#species_Cuprite">cuprite</a></td></tr> -<tr><td class="l">Orange </td><td class="l">3.5 </td><td class="l">white to yellowish </td><td class="l"> </td><td class="l"><a href="#species_Pyromorphite">pyromorphite</a></td></tr> -<tr><td class="l"> </td><td class="l">1-1½ </td><td class="l">orange </td><td class="l"> </td><td class="l"><a href="#species_Realgar">realgar</a></td></tr> -<tr><td class="l">Blue </td><td class="l">5.5-6 </td><td class="l">white </td><td class="l">in igneous rocks </td><td class="l"><a href="#species_Sodalite">sodalite</a></td></tr> -<tr><td class="l"><span class="hst">azure</span> </td><td class="l">4 </td><td class="l">azure </td><td class="l"> </td><td class="l"><a href="#species_Azurite">azurite</a></td></tr> -<tr><td class="l"><span class="hst">sky</span> </td><td class="l">7 & 4.5 </td><td class="l">white </td><td class="l">blade-like crystals </td><td class="l"><a href="#species_Cyanite">cyanite</a></td></tr> -<tr><td class="l"><span class="hst">turquoise</span> </td><td class="l">6 </td><td class="l">blue </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Turquois">turquois</a></td></tr> -<tr><td class="l"> </td><td class="l">2-4 </td><td class="l">white </td><td class="l"> </td><td class="l"><a href="#species_Chrysocolla">chrysocolla</a></td></tr> -<tr><td class="l">Green</td></tr> -<tr><td class="l"><span class="hst">malachite</span> </td><td class="l">3.5 </td><td class="l">lighter green </td><td class="l"> </td><td class="l"><a href="#species_Malachite">malachite</a></td></tr> -<tr><td class="l"><span class="hst">olive</span> </td><td class="l">6.5-7 </td><td class="l">white </td><td class="l">in igneous rocks </td><td class="l"><a href="#species_Olivine">olivine</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">white to yellow </td><td class="l"> </td><td class="l"><a href="#species_Pyromorphite">pyromorphite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">white </td><td class="l">mica-like cleavage </td><td class="l"><a href="#species_Chlorite">chlorite</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">white </td><td class="l">greasy feel, color light to dark olive green </td><td class="l"><a href="#species_Talc">talc</a></td></tr> -<tr><td class="l"><span class="hst">yellowish</span> </td><td class="l">6.5 </td><td class="l">white </td><td class="l"> </td><td class="l"><a href="#species_Epidote">epidote</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5-4 </td><td class="l">white </td><td class="l">color yellow green to olive </td><td class="l"><a href="#species_Serpentine">serpentine</a></td></tr> -<tr><td class="l">Yellow</td></tr> -<tr><td class="l"><span class="hst">golden</span> </td><td class="l">2.5 </td><td class="l">shining </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Gold">gold</a></td></tr> -<tr><td class="l"><span class="hst">brassy</span> </td><td class="l">6 </td><td class="l">greenish-black </td><td class="l">usually crystalline </td><td class="l"><a href="#species_Pyrite">pyrite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">greenish-gray </td><td class="l">color pale brassy yellow, usually non-crystalline </td><td class="l"><a href="#species_Marcasite">marcasite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">greenish-black </td><td class="l">colors nitric acid green </td><td class="l"><a href="#species_Millerite">millerite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">greenish-black </td><td class="l">color golden similar to gold </td><td class="l"><a href="#species_Chalcopyrite">chalcopyrite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">dark brown </td><td class="l">purplish tarnish on surface </td><td class="l"><a href="#species_Tetrahedrite">tetrahedrite</a></td></tr> -<tr><td class="l"><span class="hst">bronze</span> </td><td class="l">5.5 </td><td class="l">pale brownish-black </td><td class="l">color with coppery cast </td><td class="l"><a href="#species_Niccolite">niccolite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">dark gray-black </td><td class="l">with speedy black tarnish </td><td class="l"><a href="#species_Pyrrhotite">pyrrhotite</a></td></tr> -<tr><td class="l"> </td><td class="l">3 </td><td class="l">gray-black </td><td class="l">brownish with bluish tarnish </td><td class="l"><a href="#species_Bornite">bornite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">shining </td><td class="l">coppery red color </td><td class="l"><a href="#species_Copper">copper</a></td></tr> -<tr><td class="l"><span class="hst">sulphur</span> </td><td class="l">3.5 </td><td class="l">white to yellowish </td><td class="l">compact masses </td><td class="l"><a href="#species_Pyromorphite">pyromorphite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">yellow </td><td class="l"> </td><td class="l"><a href="#species_Sulphur">sulphur</a></td></tr> -<tr><td class="l"> </td><td class="l">1-3 </td><td class="l"> </td><td class="l">earthy masses </td><td class="l"><a href="#species_Carnotite">carnotite</a></td></tr> -<tr class="pbtr"><td colspan="5"> -</td></tr> -<tr><td class="l">Brown</td></tr> -<tr><td class="l"><span class="hst">violet</span> </td><td class="l">1½ </td><td class="l">shining </td><td class="l">tarnishes black </td><td class="l"><a href="#species_Cerargyrite">cerargyrite</a></td></tr> -<tr><td class="l"><span class="hst">yellowish</span> </td><td class="l">7.5 </td><td class="l">white </td><td class="l">4-sided prisms </td><td class="l"><a href="#species_Zircon">zircon</a></td></tr> -<tr><td class="l"> </td><td class="l">6.5 </td><td class="l">gray </td><td class="l"> </td><td class="l"><a href="#species_Cassiterite">cassiterite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">ochre yellow </td><td class="l">compact to earthy masses </td><td class="l"><a href="#species_Limonite">limonite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">brownish-yellow </td><td class="l"> </td><td class="l"><a href="#species_Goethite">goethite</a></td></tr> -<tr><td class="l"> </td><td class="l">4.5 </td><td class="l">black </td><td class="l"> </td><td class="l"><a href="#species_Wolframite">wolframite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">yellowish-brown </td><td class="l"> </td><td class="l"><a href="#species_Sphalerite">sphalerite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">white </td><td class="l"> </td><td class="l"><a href="#species_Siderite">siderite</a></td></tr> -<tr><td class="l"><span class="hst">grayish</span> </td><td class="l">7.5 </td><td class="l">white </td><td class="l">often twinned </td><td class="l"><a href="#species_Staurolite">staurolite</a></td></tr> -<tr><td class="l"> </td><td class="l">6.5 </td><td class="l">pale brown </td><td class="l"> </td><td class="l"><a href="#species_Rutile">rutile</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">white to yellowish </td><td class="l">earthy masses </td><td class="l"><a href="#species_Pyromorphite">pyromorphite</a></td></tr> -<tr><td class="l"><span class="hst">reddish</span> </td><td class="l">7 </td><td class="l">white </td><td class="l">dodecahedrons & trapezohedrons </td><td class="l"><a href="#species_Garnet">garnet</a></td></tr> -<tr><td class="l">Black </td><td class="l">6.5 </td><td class="l">gray </td><td class="l"> </td><td class="l"><a href="#species_Cassiterite">cassiterite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">reddish-brown </td><td class="l"> </td><td class="l"><a href="#species_Franklinite">franklinite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">black </td><td class="l">magnetic </td><td class="l"><a href="#species_Magnetite">magnetite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">dark brown </td><td class="l"> </td><td class="l"><a href="#species_Chromite">chromite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">black </td><td class="l">yellow precipitate in sulphuric acid </td><td class="l"><a href="#species_Wolframite">wolframite</a></td></tr> -<tr><td class="l"> </td><td class="l">5-6 </td><td class="l">black </td><td class="l">non-magnetic </td><td class="l"><a href="#species_Ilmenite">ilmenite</a></td></tr> -<tr><td class="l"> </td><td class="l">5-6 </td><td class="l">brownish-black </td><td class="l">compact masses </td><td class="l"><a href="#species_Psilomelane">psilomelane</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">brownish-yellow </td><td class="l">surface often brownish </td><td class="l"><a href="#species_Goethite">goethite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">dark brown </td><td class="l">tetrahedrons </td><td class="l"><a href="#species_Tetrahedrite">tetrahedrite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">silvery </td><td class="l">fresh surfaces silver color </td><td class="l"><a href="#species_Silver">silver</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">scarlet </td><td class="l">fresh surfaces bright red </td><td class="l"><a href="#species_Prousite">prousite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">purplish red </td><td class="l">fresh surfaces red </td><td class="l"><a href="#species_Pyrargyrite">pyrargyrite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">black </td><td class="l">earthy masses </td><td class="l"><a href="#species_Pyrolusite">pyrolusite</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">steel gray </td><td class="l">greasy feel </td><td class="l"><a href="#species_Graphite">graphite</a></td></tr> -<tr><td class="l">Metallic Gray </td><td class="l">2.5 </td><td class="l">black </td><td class="l">tarnishes black, bluish, or green </td><td class="l"><a href="#species_Chalcocite">chalcocite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">lead gray </td><td class="l">sectile </td><td class="l"><a href="#species_Argentite">argentite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">lead gray </td><td class="l">cubic cleavage </td><td class="l"><a href="#species_Galena">galena</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">lead gray </td><td class="l">long prismatic crystals </td><td class="l"><a href="#species_Stibnite">stibnite</a></td></tr> -<tr><td class="l"> </td><td class="l">1.5 </td><td class="l">bluish gray </td><td class="l">in scales </td><td class="l"><a href="#species_Molybdenite">molybdenite</a></td></tr> -<tr><td class="l"><span class="hst">steel</span> </td><td class="l">5.5 </td><td class="l">gray black </td><td class="l">rose color in nitric acid </td><td class="l"><a href="#species_Smaltite">smaltite</a></td></tr> -<tr><td class="l"> </td><td class="l">4.5 </td><td class="l">steel gray </td><td class="l">very heavy </td><td class="l"><a href="#species_Platinum">platinum</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">reddish black </td><td class="l">often in striated prisms </td><td class="l"><a href="#species_Manganite">manganite</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">gray </td><td class="l">with greasy feel </td><td class="l"><a href="#species_Graphite">graphite</a></td></tr> -<tr><td class="l"><span class="hst">silvery</span> </td><td class="l">5.5 </td><td class="l">black </td><td class="l"> </td><td class="l"><a href="#species_Arsenopyrite">arsenopyrite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">silvery </td><td class="l">tarnishes black on exposure </td><td class="l"><a href="#species_Silver">silver</a></td></tr> -<tr><td class="l"><span class="hst">reddish</span> </td><td class="l">5.5 </td><td class="l">gray black </td><td class="l">rose color in nitric acid </td><td class="l"><a href="#species_Cobaltite">cobaltite</a></td></tr> -<tr><td class="l"><span class="hst">pearly</span> </td><td class="l">1-1½ </td><td class="l">shining </td><td class="l">exposed surfaces violet brown </td><td class="l"><a href="#species_Cerargyrite">cerargyrite</a></td></tr> -<tr><td class="l">White, with impurities </td><td class="l">4 </td><td class="l">white </td><td class="l">porcelainous masses, effervesces in acid </td><td class="l"><a href="#species_Magnesite">magnesite</a></td></tr> -<tr><td class="l"><span class="hst">grayish or yellowish</span> </td><td class="l">2 </td><td class="l">white </td><td class="l">earthy masses, greasy feel </td><td class="l"><a href="#species_Kaolinite">kaolinite</a></td></tr> -<tr><td class="l"> </td><td class="l">1-3 </td><td class="l">white </td><td class="l">earthy masses </td><td class="l"><a href="#species_Bauxite">bauxite</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">white </td><td class="l">greasy feel, fibrous or scaly </td><td class="l"><a href="#species_Talc">talc</a></td></tr> -</table> -<div class="pb" id="Page_27">27</div> -<table class="center" summary=""> -<tr class="th"><th colspan="4">TRANSPARENT OR TRANSLUCENT COLORS</th></tr> -<tr class="th"><th><span class="sc">Color</span> </th><th><span class="sc">Hardness</span> </th><th><span class="sc">Remarks</span> </th><th><span class="sc">Mineral</span></th></tr> -<tr><td colspan="4" class="l">Colorless or with faint tinges of color due to impurities</td></tr> -<tr><td class="l"> </td><td class="l">10 </td><td class="l">in octahedrons </td><td class="l"><a href="#species_Diamond">diamond</a></td></tr> -<tr><td class="l"> </td><td class="l">9 </td><td class="l">in hexagonal prisms </td><td class="l"><a href="#species_Corundum">corundum</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">in hexagonal prisms </td><td class="l"><a href="#species_Topaz">topaz</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">in three-sided prisms </td><td class="l"><a href="#species_Tourmaline">tourmaline</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">in hexagonal prisms </td><td class="l"><a href="#species_Quartz">quartz</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Chalcedony">chalcedony</a></td></tr> -<tr><td class="l"> </td><td class="l">7 or 4.5 </td><td class="l">cubes with beveled edges </td><td class="l"><a href="#species_Boracite">boracite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">non-crystalline, pearly luster </td><td class="l"><a href="#species_Opal">opal</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">rhombohedrons </td><td class="l"><a href="#species_Willemite">willemite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">trapezohedrons </td><td class="l"><a href="#species_Analcite">analcite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">tufts of needle-like crystals </td><td class="l"><a href="#species_Natrolite">natrolite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">sheaf-like bundles of crystals </td><td class="l"><a href="#species_Stilbite">stilbite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">hexagonal prisms with basal cleavage </td><td class="l"><a href="#species_Apatite">apatite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">effervesces in acid </td><td class="l"><a href="#species_Smithsonite">smithsonite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">becomes jelly-like in acid </td><td class="l"><a href="#species_Calamine">calamine</a></td></tr> -<tr><td class="l"> </td><td class="l">4.5 </td><td class="l">monoclinic prisms </td><td class="l"><a href="#species_Colemanite">colemanite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">in cubes </td><td class="l"><a href="#species_Fluorite">fluorite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, but one cleavage </td><td class="l"><a href="#species_Aragonite">aragonite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, heavy </td><td class="l"><a href="#species_Cerrusite">cerrusite</a></td></tr> -<tr><td class="l"> </td><td class="l">3 </td><td class="l">effervesces in acid, rhomboidal cleavage </td><td class="l"><a href="#species_Calcite">calcite</a></td></tr> -<tr><td class="l"> </td><td class="l">3 </td><td class="l">no effervescence, but soluble in nitric acid </td><td class="l"><a href="#species_Anglesite">anglesite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">in cubes tastes of salt </td><td class="l"><a href="#species_Halite">halite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">soluble in water, sweetish taste </td><td class="l"><a href="#species_Borax">borax</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">1 perfect cleavage, and two imperfect cleaves at 66 with each other </td><td class="l"><a href="#species_Gypsum">gypsum</a></td></tr> -<tr><td colspan="4" class="l">White or with faint tinges of color due to impurities, such as pink, bluish, etc.</td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Quartz">quartz</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Chalcedony">chalcedony</a></td></tr> -<tr><td class="l"> </td><td class="l">7 or 4.5 </td><td class="l">cubes with beveled edges </td><td class="l"><a href="#species_Boracite">boracite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">non-crystalline, pearly luster </td><td class="l"><a href="#species_Opal">opal</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">cleavage in 3 directions, good in 2 and imperfect in the other </td><td class="l"><a href="#species_Feldspar">feldspar</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">short eight-sided prisms </td><td class="l"><a href="#species_Pyroxene">pyroxene</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">long six-sided prisms </td><td class="l"><a href="#species_Amphibole">amphibole</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">trapezohedrons </td><td class="l"><a href="#species_Analcite">analcite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">tufts of needle-like crystals </td><td class="l"><a href="#species_Natrolite">natrolite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">sheaf-like bundles of crystals </td><td class="l"><a href="#species_Stilbite">stilbite</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">rhombohedrons </td><td class="l"><a href="#species_Willemite">willemite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">effervesces in acid </td><td class="l"><a href="#species_Smithsonite">smithsonite</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">becomes jelly-like in acid </td><td class="l"><a href="#species_Calamine">calamine</a></td></tr> -<tr><td class="l"> </td><td class="l">4.5 & 7 </td><td class="l">cubes with beveled edges </td><td class="l"><a href="#species_Boracite">boracite</a></td></tr> -<tr><td class="l"> </td><td class="l">4.5 </td><td class="l">monoclinic prisms </td><td class="l"><a href="#species_Colemanite">colemanite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">effervesces in acid, porcelainous </td><td class="l"><a href="#species_Magnesite">magnesite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5-4 </td><td class="l">effervesces in acid, heavy, red color in flame </td><td class="l"><a href="#species_Strontianite">strontianite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, heavy, green color in flame </td><td class="l"><a href="#species_Witherite">witherite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in warm acid, rhomboidal cleavage </td><td class="l"><a href="#species_Dolomite">dolomite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, cleavage in one direction only </td><td class="l"><a href="#species_Aragonite">aragonite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, heavy, does not color flame </td><td class="l"><a href="#species_Cerrusite">cerrusite</a></td></tr> -<tr><td class="l"> </td><td class="l">3-3.5 </td><td class="l">no effervescence, cleavage in three directions at right angles </td><td class="l"><a href="#species_Anhydrite">anhydrite</a></td></tr> -<tr class="pbtr"><td colspan="5"> -</td></tr> -<tr><td class="l"> </td><td class="l">3 </td><td class="l">effervesces in acid, rhomboidal cleavage </td><td class="l"><a href="#species_Calcite">calcite</a></td></tr> -<tr><td class="l"> </td><td class="l">3 </td><td class="l">tabular crystals, heavy, green color in flame </td><td class="l"><a href="#species_Barite">barite</a></td></tr> -<tr><td class="l"> </td><td class="l">2-3 </td><td class="l">cleaves in thin elastic sheets </td><td class="l"><a href="#species_Mica">mica</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">cleaves in cubes </td><td class="l"><a href="#species_Cryolite">cryolite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5 </td><td class="l">cubes, soluble in water, salty taste </td><td class="l"><a href="#species_Halite">halite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">1 perfect cleavage, and 2 less perfect ones </td><td class="l"><a href="#species_Gypsum">gypsum</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">cleaves in thin non-elastic sheets </td><td class="l"><a href="#species_Chlorite">chlorite</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">soluble in water, tastes sweet </td><td class="l"><a href="#species_Borax">borax</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">greasy feel </td><td class="l"><a href="#species_Talc">talc</a></td></tr> -<tr><td class="l">Green </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">oriental emerald</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">octahedrons </td><td class="l"><a href="#species_Spinel">spinel</a></td></tr> -<tr><td class="l"> </td><td class="l">7.5 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Beryl">beryl</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">three-sided prisms </td><td class="l"><a href="#species_Tourmaline">tourmaline</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">dodecahedrons or trapezohedrons </td><td class="l"><a href="#species_Garnet">garnet</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Prase">prase</a> or <a href="#species_Plasma">plasma</a></td></tr> -<tr><td class="l"> </td><td class="l">6.5-7 </td><td class="l">non-crystalline, olive color </td><td class="l"><a href="#species_Olivine">olivine</a></td></tr> -<tr><td class="l"> </td><td class="l">6.5 </td><td class="l">yellow green color, rather opaque </td><td class="l"><a href="#species_Epidote">epidote</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">non-crystalline, pearly luster </td><td class="l"><a href="#species_Opal">opal</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">short eight-sided prisms </td><td class="l"><a href="#species_Pyroxene">pyroxene</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">long six-sided prisms </td><td class="l"><a href="#species_Amphibole">amphibole</a></td></tr> -<tr><td class="l"> </td><td class="l">5 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Apatite">apatite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">cubes </td><td class="l"><a href="#species_Fluorite">fluorite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid </td><td class="l"><a href="#species_Cerrusite">cerrusite</a></td></tr> -<tr><td class="l"> </td><td class="l">2.5-4 </td><td class="l">somewhat greasy feel, massive or fibrous </td><td class="l"><a href="#species_Serpentine">serpentine</a></td></tr> -<tr><td class="l"> </td><td class="l">2 </td><td class="l">in mica-like scales, non-elastic </td><td class="l"><a href="#species_Chlorite">chlorite</a></td></tr> -<tr><td class="l"> </td><td class="l">1 </td><td class="l">greasy feel, fibrous or scaly </td><td class="l"><a href="#species_Talc">talc</a></td></tr> -<tr><td class="l">Red </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">ruby</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">octahedrons </td><td class="l"><a href="#species_Spinel">spinel</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">three-sided prisms </td><td class="l"><a href="#species_Tourmaline">tourmaline</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">dodecahedrons or trapezohedrons </td><td class="l"><a href="#species_Garnet">garnet</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">hexagonal </td><td class="l"><a href="#species_RoseQuartz">rose quartz</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Jasper">jasper</a> or <a href="#species_Carnelian">carnelian</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">pearly luster </td><td class="l"><a href="#species_FireOpal">fire opal</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">cubes, rose tints </td><td class="l"><a href="#species_Fluorite">fluorite</a></td></tr> -<tr><td class="l"> </td><td class="l">2-3 </td><td class="l">pink mica-like scales </td><td class="l"><a href="#species_Mica">lepidolite</a></td></tr> -<tr><td class="l">Blue </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">sapphire</a></td></tr> -<tr><td class="l"> </td><td class="l">7 & 4.5 </td><td class="l">blade-like crystals </td><td class="l"><a href="#species_Cyanite">cyanite</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">non-crystalline masses </td><td class="l"><a href="#species_Turquois">turquois</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5-6 </td><td class="l">in igneous rocks </td><td class="l"><a href="#species_Sodalite">sodalite</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">azure color </td><td class="l"><a href="#species_Azurite">azurite</a></td></tr> -<tr><td class="l"> </td><td class="l">3.5 </td><td class="l">effervesces in acid, heavy </td><td class="l"><a href="#species_Cerrusite">cerrusite</a></td></tr> -<tr><td class="l"> </td><td class="l">2-4 </td><td class="l">earthy masses, turquoise color </td><td class="l"><a href="#species_Chrysocolla">chrysocolla</a></td></tr> -<tr><td class="l">Violet </td><td class="l">7 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Amethyst">amethyst</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">cubes </td><td class="l"><a href="#species_Fluorite">fluorite</a></td></tr> -<tr><td class="l">Yellow </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">oriental topaz</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">octahedrons </td><td class="l"><a href="#species_Spinel">spinel</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Topaz">topaz</a></td></tr> -<tr><td class="l"> </td><td class="l">4 </td><td class="l">cubes </td><td class="l"><a href="#species_Fluorite">fluorite</a></td></tr> -<tr><td class="l">Brown </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">corundum</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">octahedrons </td><td class="l"><a href="#species_Spinel">spinel</a></td></tr> -<tr><td class="l"> </td><td class="l">7.5 </td><td class="l">four-sided prisms </td><td class="l"><a href="#species_Zircon">zircon</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_SmokyQuartz">smoky quartz</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">three-sided prisms </td><td class="l"><a href="#species_Tourmaline">tourmaline</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Flint">flint</a></td></tr> -<tr><td class="l"> </td><td class="l">6 </td><td class="l">non-crystalline </td><td class="l"><a href="#species_Opal">opal</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">short eight-sided prisms </td><td class="l"><a href="#species_Pyroxene">pyroxene</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">long six-sided prisms </td><td class="l"><a href="#species_Amphibole">amphibole</a></td></tr> -<tr><td class="l"> </td><td class="l">2-3 </td><td class="l">cleaves into thin sheets </td><td class="l"><a href="#species_Mica">mica</a></td></tr> -<tr><td class="l">Black </td><td class="l">9 </td><td class="l">hexagonal prisms </td><td class="l"><a href="#species_Corundum">corundum</a></td></tr> -<tr><td class="l"> </td><td class="l">8 </td><td class="l">octahedrons </td><td class="l"><a href="#species_Spinel">spinel</a></td></tr> -<tr><td class="l"> </td><td class="l">7 </td><td class="l">three-sided prisms </td><td class="l"><a href="#species_Tourmaline">tourmaline</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">short eight-sided prisms </td><td class="l"><a href="#species_Pyroxene">pyroxene</a></td></tr> -<tr><td class="l"> </td><td class="l">5.5 </td><td class="l">long six-sided prisms </td><td class="l"><a href="#species_Amphibole">amphibole</a></td></tr> -<tr><td class="l"> </td><td class="l">2-3 </td><td class="l">cleaves in thin sheets </td><td class="l"><a href="#species_Mica">mica</a></td></tr> -</table> -<div class="pb" id="Page_29">29</div> -<h3 class="center"><span class="sc">The Gold Group</span></h3> -<p>Gold was undoubtedly the first metal to be -used by primitive man; for, occurring as it did -in the stream beds, its bright color quickly -attracted the eye, and it was so soft, that it was -easily worked into various shapes, which, because -they did not tarnish, became permanent ornaments. -The metal is associated with the very -earliest civilizations, being found in such ancient -tombs as those at Kertsch in Crimea and in -northern Africa and Asia Minor. It was used -in the cloisonné work of Egypt 3000 years <span class="small">B.C.</span> -In America the Indians, especially to the south, -were using it long before the continent was -discovered.</p> -<p>Of all the metals gold is the most malleable, -and its ductility is remarkable, for a piece of a -grain’s weight (less than the size of a pin head) -can be drawn out into a wire 500 feet long; and -<span class="pb" id="Page_30">30</span> -it can be beaten into a thin leaf as thin as ¹/₂₅₀₀₀₀ -of an inch in thickness, and thus a bit, weighing -only a grain, can thus be spread over 56 square -inches.</p> -<p>It forms very few compounds, but has a -considerable tendency to make alloys (<i>i.e.</i>, mixtures -with other metals without the resulting -compound losing its metallic character). In -Nature gold is never entirely pure, but is an -alloy, usually with silver, there being from a -fraction of 1% up to 30% of the silver with the -gold, the more silver in the alloy, the paler the -color of the gold. Australian gold is the purest, -having but about .3% of silver in it, while -Californian gold has around 10% and Hungarian -gold runs as high as 30% of silver. Another -alloy fairly abundant in Nature is that with -tellurium, such as <i>calaverite</i> (AuTe₂) which is a -pale brassy yellow, similar to pyrite, but with the -hardness of but 2.5. Another combination -includes gold, silver and tellurium, <i>sylvanite</i>, -(AuAgTe₄) a silvery white mineral with a hardness -of but 2. Such combinations are known -as tellurides and the calaverite is mined as a source -of gold at Cripple Creek, Colo., while the sylvanite -is one of the important ores of gold in South -Africa. Occasionally gold is also found alloyed -with platinum, copper, iron, etc. Jewelers make -several alloys, “red gold” being 3 parts gold and -1 of copper, “green gold” being the same proportions -of gold and silver, and “blue gold” -being the combination of gold and iron. Our -gold coins are alloys, nine parts gold and one of -copper, to give them greater durability. Most of -<span class="pb" id="Page_31">31</span> -the gold recovered from nature is found native, -<i>i.e.</i>, the pure metal, or with some alloy.</p> -<h3><a id="species_Gold">Gold</a> -<br />Au -<br /><a href="#Plate_5">Pl. 5</a></h3> -<p>Usually non-crystalline, but occasionally -showing cube or octahedral -faces of the isometric system; hardness -2.5; specific gravity 19.3; color golden yellow; -luster metallic; opaque.</p> -<p>Gold is mostly found as the metal and is -readily recognized by its color, considerable -weight, hardness, malleability, and the fact that -it does not tarnish. It usually occurs in quartz -veins in fine to thick threads, scales or grains, -and occasionally in larger masses termed “nuggets.” -It is insoluble in most liquids so that -when weathered from its original sites, it was -often washed down into stream beds, to be found -later in the sands or gravels, or even in the sea -beaches. When thus found it is termed “placer -gold,” and its recovery is placer mining. Most -of the original discoveries of gold have been in -these placer deposits; and from them it has -been traced back to the ledges from which it -originally weathered. In the placer deposits the -size of the particles varies from fine “dust” -up to large nuggets, the largest found in California -weighing 161 pounds; but the largest one -found in the world was the “Welcome Nugget,” -found in Australia, and weighing 248 pounds. -When gold was discovered in California in 1848, -this became the chief source for the world, but -later this distinction went to Australia, and now -belongs to South Africa, which today yields over -half the annual supply.</p> -<div class="pb" id="Page_32">32</div> -<p>The ultimate source of gold is from the lighter -colored igneous rocks, like granites, syenites, -and diorites, throughout which it is diffused in -quantities too small to be either visible or worth -while to extract. It becomes available only -when it has been dissolved out by percolating -waters and segregated in fissures or veins, either -in or leading from these igneous rocks. Generally -this transfer of gold has taken place when -the rocks were at high temperatures, and by the -aid of water (and perhaps other solvents) which -was also at high temperatures. The presence -of gold in sandstones, limestones, etc., is secondary, -as is also its presence in sea water, in which -there is reported to be nearly a grain (about five -cents worth) in every ton of water. Beside the -direct recovery of gold from gold mining, a great -deal is obtained from its association with iron, -copper, silver, lead and zinc sulphides, in which -it is included in particles too fine to be visible, -but in quantities large enough to be separated -from the other metals after they are smelted.</p> -<p>In the United States gold is found in the -Cordilleran region from California to Alaska, in -Colorado, Nevada, Arizona, Utah, the Black -Hills of South Dakota, and in small quantities -in the metamorphosed slates of North and South -Carolina, Georgia, and in Nova Scotia.</p> -<h3 class="center"><span class="sc">The Silver Group</span></h3> -<p>Though much commoner than gold, silver did -not attract the eye of man as early, probably -because it tarnishes when exposed to air or any -other agent having sulphur compounds in it, -<span class="pb" id="Page_33">33</span> -and a black film of silver sulphide covers the -surface. Its first use was for ornaments, and -some of these found in the ruins of ancient Troy -indicate its use as early as 2500 <span class="small">B.C.</span> A thousand -years later it was being used to make basins, -vases and other vessels.</p> -<p>Silver is next to gold in malleability and -ductility, so that a grain of silver can be drawn -out into a wire 400 feet long, or beaten into -leaves ¹/₁₀₀₀₀₀ of an inch in thickness. As a -conductor of electricity it is unsurpassed, being -rated at 100% while copper rates 93%. Silver -is also like gold in the freedom with which it -alloys with other metals, such as gold, copper, -iron, platinum, etc. All our silver coins, tableware, -etc., have some copper alloyed with the -silver to give it greater hardness and durability.</p> -<p>Unlike gold, silver freely enters into compounds -with the non-metals, which is the reason -that it is not found primarily in its native state, -but usually as a sulphide. Its ultimate source -is in the igneous rocks, few granites or lavas, on -analysis, failing to show at least traces of silver. -Before it is available as an ore, or mineral, it has -been dissolved from the original magma, and -segregated in fissures or veins, along with such -minerals, as quartz, fluorite, calcite, etc. This -seems to have taken place while the igneous -rocks were still hot, and by the agency of vapors -and liquids which were also hot. The presence -of silver in sedimentary and metamorphic rocks, -or even in sea water, is secondary.</p> -<p>The primary deposition of silver is usually in -the form of sulphides, the commoner of which -<span class="pb" id="Page_34">34</span> -are, argentite or silver sulphide, pyrargyrite -or silver and antimony sulphide, and prousite, or -silver and arsenic sulphide. Its occurrence as -native silver, or the chloride, cerargyrite, is -secondary and due to the reactions which have -taken place when sulphide deposits have been -subjected to weathering agents.</p> -<p>The United States produces about 25% of the -world’s supply, Mexico some 35%. It is especially -found along the Cordilleran ranges of both -North and South America.</p> -<h3><a id="species_Silver">Silver</a> -<br />Ag -<br /><a href="#Plate_6">Pl. 6</a></h3> -<p>Usually non-crystalline, but -occasionally showing cube or octahedron -faces of the isometric system; -hardness 2.5; specific gravity 10.5; color silvery -white; luster metallic; opaque.</p> -<p>When found in its native state silver is usually -in wirey, flakey, or mossy masses; but sometimes -masses of considerable size occur, the most -famous being an 800 pound nugget found in Peru, -and another of 500 pounds weight found at -Konsberg, Norway, and now preserved in Copenhagen. -When exposed to the air the surface -soon tarnishes and takes on a black color which -must be scraped off to see the real color.</p> -<p>Like gold, silver is usually found associated -with other metals, like iron, copper, lead and -zinc; and much of the silver recovered is obtained -in connection with the mining, especially -of copper and lead. Some lead ores have so -much silver in them that they are better worth -mining for the silver; galena, for instance, under -such circumstances being termed argentiferous -<span class="pb" id="Page_35">35</span> -galena. Native silver is a secondary mineral, -having been formed by the reduction of some one -of its sulphides by water, carrying various elements -which had a greater affinity for the sulphur.</p> -<p>Silver is found along with copper in the Lake -Superior region, and in Idaho, Nevada, and -California.</p> -<h3><a id="species_Argentite">Argentite</a> -<br />AgS -<br /><a href="#Plate_6">Pl. 6</a> -<br /><i>silver glance</i></h3> -<p>Usually in irregular masses, but -sometimes in cubes; hardness 2.5; -specific gravity 7.3; color and streak -lead gray; luster metallic; opaque on thin edges.</p> -<p>Argentite, the simple sulphide of silver, is the -chief source from which silver is obtained. It -looks like galena, and has the same hardness, -streak and specific gravity, but can be distinguished -by the galena having a very perfect -cubic cleavage while the argentite has no cleavage. -Argentite is easily cut with a knife (sectile). -It is usually found in irregular masses, but sometimes -in cubes which make very choice cabinet -specimens; and is associated with such other -minerals as galena, sphalerite, chalcopyrite, -pyrite, fluorite, quartz, and calcite.</p> -<p>It occurs in fissures and veins all through the -Cordilleran regions, especially in California, -Colorado, Nevada (Comstock Lode), Arizona -(Silver King Mine) and about the shores of -Lake Superior.</p> -<h3><a id="species_Pyrargyrite">Pyrargyrite</a> -<br />Ag₃SbS₃ -<br /><a href="#Plate_7">Pl. 7</a> -<br /><i>ruby silver</i> or <i>dark red silver</i></h3> -<p>Usually occurs in irregular masses; -hardness 2.5; specific gravity 5.8; -color dark red to black; streak purplish -red; luster metallic to adamantine; -translucent on thin edges.</p> -<div class="pb" id="Page_36">36</div> -<p>Pyrargyrite, the sulphide of silver and antimony, -is distinguished by its dark red color and -the purplish streak. It may look like prousite, -but is easily distinguished from the latter which -has a scarlet streak. It also at times looks like -hematite and cinnabar, but the hematite has a -hardness of 6, and the latter has the bright red -color throughout, while pyrargyrite turns black -when exposed to the light, so that the characteristic -red color will be seen only on fresh -surfaces. The characteristic red color can only -be kept on the mineral if it is constantly protected -from the light.</p> -<p>Sometimes pyrargyrite occurs in crystals and -these belong to the hexagonal system, and are -prisms with low faces on the ends, as on <a href="#Plate_7">plate 7</a>, -and the mineral is peculiar in that the faces on -the opposite ends are unlike.</p> -<p>Pyrargyrite is found mostly in fissures and -veins of quartz, fluorite, calcite, etc., and associated -with pyrite, chalcopyrite, galena, etc. -It is fairly common in Colorado in Gunnison -and Ouray counties, in Nevada, New Mexico, -Arizona, etc.</p> -<h3><a id="species_Prousite">Prousite</a> -<br />Ag₃ AsS₃ -<br /><a href="#Plate_7">Pl. 7</a> -<br /><i>light red</i> -<br /><i>silver</i></h3> -<p>Usually occurs in irregular masses; -hardness 2.5; specific gravity 5.6; -color scarlet to vermilion; streak -the same; luster adamantine; transparent -on thin edges.</p> -<p>In general this mineral is very like pyrargyrite, -but has the scarlet color and streak which are -entirely characteristic. It is likely to have the -surface tarnished black, which happens on exposure -<span class="pb" id="Page_37">37</span> -to light, so that it is essential to be sure -that fresh surfaces are being examined. Occasionally -it is found in crystals, of the same -type as the preceding mineral. It is generally -found associated with pyrargyrite.</p> -<h3><a id="species_Cerargyrite">Cerargyrite</a> -<br />AgCl -<br /><i>horn silver</i></h3> -<p>Usually found in irregular masses -or incrustations; hardness 1 to 1½; -specific gravity 5.5; color pearly gray, -grayish green to colorless, but turning violet -brown on exposure to light; luster resinous; -transparent on thin edges.</p> -<p>This mineral is usually found in thin seams -or waxy incrustations, but it may occur in crystals -in which case they are cubes. It is very -soft and easily cut with a knife, which with its -tendency to turn violet-brown on exposure to -light, makes it easy to identify. Cerargyrite is a -secondary mineral, resulting from the action of -chlorine-bearing water on some one of the -sulphides of silver. It is found in the upper -portions of mines, especially those in arid regions.</p> -<h3 class="center"><span class="sc">The Copper Group</span></h3> -<p>After gold the next metal to be utilized was -copper. About 4000 <span class="small">B.C.</span> our early forefathers -found that by heating certain rocks, they obtained -a metal which could be pounded, ground -and carved into useful shapes. Curiously enough -the rocks which had the copper also had some -tin in them, so that this first-found copper was -not pure, but had from five to ten per cent of tin -in it, making the resulting metal harder, and -<span class="pb" id="Page_38">38</span> -what we call bronze. It was some thousands of -years later before they distinguished the copper -as a pure metal, but it worked and made good -tools. The newly found metal was not as ornamental -as gold; but, because it could be made -into tools, it had a tremendous influence on -man’s development. As the bronze tools began -to take the place of the stone implements, the -“Age of Bronze” was ushered in. In America -the Indians in the Lake Superior region found -native copper weathered out of the rocks and -later mined it, and they too pounded it into -knives, axes, needles, and ornaments, but probably -never learned to melt it and mold their -tools. At any rate they were not as far advanced -in using this metal when Columbus -landed as were the southern Europeans 6500 -years earlier. Since the use of iron became -general, copper has not held such a dominant -place, but it still is “the red metal” which holds -the second most important place.</p> -<p>It is malleable and ductile, though not equal -to gold or silver in these respects. It is a good -conductor of electricity and a very large amount -of copper is used in electrical manufacture, -roofing, wire, etc. It alloys with other metals; -ten parts copper and one of tin being bronze, ten -of copper and one of zinc is brass, and copper -with aluminum is aluminum bronze.</p> -<p>Like silver and gold, copper is widely diffused -through the igneous rocks, but before it is available, -it must be leached out by solvents and concentrated -in veins, fissures, or definite parts of -the lavas or granites. The primary ores are -<span class="pb" id="Page_39">39</span> -those which, while the igneous rock was still -hot, were carried by hot vapors and liquids into -the fissures and there deposited, mostly as sulphides. -There is a long list of these, but in this -country, the following are the commoner ones; -chalcocite the sulphide of copper, chalcopyrite -the sulphide of copper and iron, bornite another -combination of copper, iron and sulphur, and -tetrahedrite copper and antimony sulphide. -When these primary ores are near enough to the -surface to come in contact with waters carrying -oxygen, carbon dioxide or silica in solution, they -may give up their sulphur and take some one of -these new elements and we have such forms as -cuprite, the oxide of copper, malachite and -azurite, carbonates of copper, or chrysocolla, -the silicate of copper. Native copper is also a -secondary deposit laid down in its present state -by a combination of circumstances which deprived -it of its original sulphur. In general -copper mining can not be profitably carried on -for ores with anything less than a half of one -percent in them; and the use of such low grade -ores has only been possible for a few years, as -the result of inventing most delicate processes -in the smelting.</p> -<p>The United States produces about a quarter of -the world’s supply of copper, with Chile ranking -second with about 17%.</p> -<h3><a id="species_Copper">Copper</a> -<br />Cu -<br /><a href="#Plate_8">Pl. 8</a></h3> -<p>Usually in irregular masses; hardness -2.5; specific gravity 8.9; color -copper red; luster metallic; opaque. -Native copper, easily determined by its color -<span class="pb" id="Page_40">40</span> -and hardness, is generally found in irregular -grains, sheets, or masses, on which may sometimes -be detected traces of a cube or an octahedral -face, showing that it belongs to the -isometric system. The most famous locality is -the Upper Peninsula of Michigan which may be -taken as typical. Here, long before it was known -historically, the Indians found and dug out copper -to make knives, awls, and ornaments.</p> -<p>In this region, beds of lava alternate with -sandstones and conglomerates. The copper was -originally in the lavas, but has been dissolved -out, and now fills cracks and gas cavities in the -lavas, and also the spaces between the pebbles -of the conglomerate. This locality has been -very famous both because of the quantity mined, -and also because of the strikingly large masses -sometimes found. Today but little of the ore -runs above 2 percent copper, and it is mined -if it has as little as ½ of one percent.</p> -<p>While nowhere near as abundant, native -copper occurs in the same way in cavities and -cracks in the trap rocks of New Jersey, and along -the south shore of the Bay of Fundy. It is also -known from Oregon, the White River region of -Alaska, and in Arctic Canada.</p> -<h3><a id="species_Chalcopyrite">Chalcopyrite</a> -<br />CuFeS₂ -<br /><a href="#Plate_8">Pl. 8</a> -<br /><i>copper pyrites</i> or <i>yellow copper ore</i></h3> -<p>Occurs in crystals of irregular -masses; hardness 4; specific gravity -4.2; color bronze yellow; streak -greenish black; luster metallic; -opaque on thin edges.</p> -<p>Chalcopyrite resembles pyrite, but -its color is a more golden yellow, and its surface -<span class="pb" id="Page_41">41</span> -tarnishes with iridescent colors. Then too the -hardness of chalcopyrite is but 4 as compared -with 6 for pyrite. When in crystals this mineral -belongs to the tetrahedral system as the c axis -is but .985 in length as compared with I for the -two other axes. This difference is so little that, -to the eye, the octahedron appears to belong to -the isometric system. Chalcopyrite occurs in -octahedrons and tetrahedrons (as on <a href="#Plate_8">plate 8</a>), -the latter being the form where but half of -the octahedral faces are developed. However -by far the most frequent mode of occurrence -is in irregular masses.</p> -<p>This is the most important primary ore of -copper, and is widely distributed, being found -either in lavas, or in veins, or in fissures connected -with igneous rocks. Apparently the -deposits were made, either at the time of eruptive -disturbances or shortly afterward, from -vapors or hot solutions carrying the copper -sulphides (and other sulphides) from the molten -igneous rocks. Chalcopyrite is usually associated -with pyrite, galena, sphalerite and chalcocite, as -well as quartz, fluorite and calcite. It is found in -all the New England States, in New York, New -Jersey, Pennsylvania, Maryland, Virginia, North -Carolina, Tennessee, Missouri, and all the Rocky -Mountain and Pacific Coast States.</p> -<h3><a id="species_Bornite">Bornite</a> -<br />Cu₃FeS₃ -<br /><i>purple copper ore</i></h3> -<p>Occurs in granular or compact -masses; hardness 3; specific gravity, -5; color bronze-brown with a bluish -tarnish; streak gray-black; luster -metallic; opaque on thin edges.</p> -<div class="pb" id="Page_42">42</div> -<p>Bornite is also known as erubescite, blushing -ore, variegated copper, peacock copper, etc., -all of which names refer to the highly iridescent -tarnish which fresh faces soon take on when -exposed to the air. Though usually in masses, -it is sometimes found in rough cubes of the isometric -system. In this country it is not abundant -enough to be used as an ore, but is likely to be -found with other ores like chalcopyrite or chalcocite. -In the east it has been found at Bristol, -Conn., and near Wilkesbarre, Penn., while in -the west it may be expected to occur wherever -other sulphide minerals of copper are found.</p> -<h3><a id="species_Chalcocite">Chalcocite</a> -<br />Cu₂S -<br /><a href="#Plate_9">Pl. 9</a> -<br /><i>copper glance</i></h3> -<p>Occurs in fine grained compact -masses; hardness 2.5; specific gravity -5.7; color dark leaden gray; -streak black; luster metallic; opaque -on thin edges.</p> -<p>Chalcocite is one of the important ores of -copper, especially in Arizona and the Butte -District of Montana. It resembles argentite -in color and general appearance, but is readily -distinguished by being brittle and having a -tendency to tarnish to bluish or greenish colors -on fresh surfaces. Occasionally it occurs in -crystals which are in the orthorhombic system; -but the edges of the prism are so beveled that -there are six sides and the prism resembles a -hexagonal prism (see <a href="#Page_16">page 16</a>).</p> -<p>In the Butte, Mont., district, the most important -copper region in the United States, fully 50% -of the ore is chalcocite, which is a derivative of -the originally deposited chalcopyrite, the latter -<span class="pb" id="Page_43">43</span> -having lost its iron. In the veins of this district -chalcopyrite, bournite, tetrahedrite, and several -other copper minerals not described in this book, -occur all together, and with them also gold, -silver and arsenic minerals. The gold amounts -to about 2¼ cents per pound of copper, and the -silver is in somewhat less quantity. These veins -were first opened to get the silver ores, which -were the more important ones down to a depth -of 200 to 400 feet. Below these depths the -copper became much more important. It was -the weathering which had removed a large part -of the copper minerals in the upper levels of the -veins, but had left a large part of the silver. -Chalcocite is also important in most of the Utah -and Arizona mines.</p> -<p>In the east it has been found at Bristol, Simsbury -and Cheshire, Conn., and in the west it is -found in all the Cordilleran States.</p> -<h3><a id="species_Tetrahedrite">Tetrahedrite</a> -<br />Cu₃SbS₃ -<br />Pl. <a href="#Plate_9">9</a> & <a href="#Plate_10">10</a> -<br /><i>gray copper ore</i></h3> -<p>Occurs in irregular masses and in -tetrahedrons of the isometric system; -hardness 3.5; specific gravity 4.7; -streak dark brown; luster metallic; -opaque on thin edges.</p> -<p>In its crystalline form the tetrahedrite occurs -in tetrahedrons, which generally have faces -formed by beveling the edges and by cutting the -corners, as in the two figures of <a href="#Plate_10">plate 10</a>. Chalcopyrite -may also occur in tetrahedrons, but -its golden yellow color is entirely different from -the gray-black of the tetrahedrite. When in -masses the hardness and the streak which is dark -brown, are very characteristic.</p> -<div class="pb" id="Page_44">44</div> -<p>In England and Bolivia tetrahedrite is an -important ore of copper, but in this country it is -simply a copper mineral which is widely distributed, -and associated with most of the mining -enterprises, but is in no case the important ore. -It has been found sparingly through the New -England States, at the Kellogg Mines in -Arkansas, and abundantly in Colorado, Montana, -Utah, Arizona, Nevada and New Mexico.</p> -<h3><a id="species_Cuprite">Cuprite</a> -<br />Cu₂O -<br />Pl. <a href="#Plate_9">9</a> & <a href="#Plate_10">10</a> -<br /><i>red copper ore</i></h3> -<p>Occurs in isometric cubes, octahedrons, -and dodecahedrons, or in -masses; hardness 3.5; specific gravity -6; color dark brownish-red; -streak brownish-red; luster metallic; translucent -on thin edges.</p> -<p>When in crystals cuprite is easily determined, -but when in masses its fresh surfaces may suggest -prousite, but the streak and hardness are -quite different in the two cases. Sometimes its -color suggests hematite, but the latter has the -hardness of 6. When found it is often coated -with a thin film of green, which is malachite.</p> -<p>Except when found as native copper, the ore -which contains the greatest percentage of copper -is cuprite with 88.8% of copper. It is likely to -occur in any of the deposits of copper ore, where -they are in arid climates and above the level of -the underground water, and is very frequently -associated with malachite and azurite. In the -Bisbee, Arizona, district cuprite is one of the -important ores.</p> -<p>Besides the normal occurrence described -above, cuprite may be found in two other varieties; -<span class="pb" id="Page_45">45</span> -one where the crystals have grown side by -side and so only the ends have been free for -continuous additions of the mineral, which has -resulted in a fibrous mass known as “plush -copper ore” or chalcotrichite; the other an -earthy mixture of limonite and cuprite, which is -brick red in color, and termed “tile ore.”</p> -<p>Cuprite is found sparingly in New England, -more abundantly at such places as Summerville -and Flemington, N. J., Cornwall, Penn., in the -Lake Superior region, and fairly abundantly in -the Cordilleran States.</p> -<h3><a id="species_Malachite">Malachite</a> -<br />CuCO₃·Cu(OH)₂ -<br /><a href="#Plate_11">Pl. 11</a></h3> -<p>Usually occurs in nodular or incrusting -masses; hardness 3.5; -specific gravity 4; color green; streak -a lighter green; luster adamantine, silky or dull; -translucent on thin edges.</p> -<p>The vivid green of malachite is usually enough -to determine it at once, but one may be sure -by trying a drop of acid on it, in which case it -effervesces as is characteristic of so many carbonates, -but this is the only carbonate which is -vivid green. Generally the malachite is in -irregular masses, but crystals are occasionally -found. These are extremely small and needle-like, -and belong to the monoclinic system. In -the Ural Mountains there is a locality where -these crystals grow in fibrous masses, usually -radiating from the center. Malachite in such -nodules has a silky luster. These rare nodules -have furnished the rulers of Russia with a unique -and much prized material for making royal gifts. -In European museums and palaces one finds -<span class="pb" id="Page_46">46</span> -many objects carved from this form of malachite, -and marked as gifts of the czars of Russia.</p> -<p>In the United States malachite is widely -distributed, appearing as green streaks and -stains where copper minerals have been exposed -to the air. It is the green tarnish which appears -on bronze and copper when exposed to the -weather. It is found in large quantities in New -Jersey, Pennsylvania, Wisconsin, Nevada, Arizona, -Utah, New Mexico, etc. The Bisbee mine -in Arizona is the place that has furnished museums -with so many of the handsome specimens -of malachite associated with azurite. These are -the most striking specimens for the vividness of -their colors that appear in any collections.</p> -<p>Malachite has been known since about 4000 -<span class="small">B.C.</span>, the Egyptians having mines where they -obtained it between the Suez and Mt. Sinai. -In those early days it was particularly a child’s -charm, protecting the wearer from evil spirits. -It is still used as a stone of lesser value in -making some sorts of jewelry.</p> -<h3><a id="species_Azurite">Azurite</a> -<br />2CuCO₃·Cu(OH)₂ -<br /><a href="#Plate_11">Pl. 11</a></h3> -<p>Occurs as short prismatic or tabular -crystals of the monoclinic system; -hardness 4; specific gravity 3.8; -color azure blue; streak lighter blue; luster -vitreous; translucent on thin edges.</p> -<p>Azurite is another very striking mineral fully -characterized by its color and streak. Like -malachite it effervesces in acid. It is very near -to malachite in composition, and by increasing -its water content, can and freely does change to -the green mineral; so that few specimens of -<span class="pb" id="Page_47">47</span> -azurite are without traces of malachite. It is -found in the same places as malachite, but is -not as abundant in the east.</p> -<p>Azurite with the accompanying malachite is -cut and polished to make semi-precious stones -for some forms of jewelry.</p> -<h3><a id="species_Chrysocolla">Chrysocolla</a> -<br />CuSiO₃·2H₂O</h3> -<p>Never occurs in crystals, but in -seams and incrustations; hardness -2-4; specific gravity 2.1; color bluish-green; streak -white; luster vitreous; translucent on thin edges.</p> -<p>This rather rare mineral often appears in opal- -or enamel-like incrustations, and its color is -variable ranging from the typical bluish-green to -sky-blue or even turquoise blue. This is a -mineral resulting from the action of silica bearing -waters, coming in contact with most any of -the copper minerals, and is found accompanying -cuprite, malachite, azurite, etc. It is never in -large enough quantities to be used as an ore, but -its striking color attracts attention and it can be -found fairly frequently, especially in the west.</p> -<h3 class="center"><span class="sc">The Iron Group</span></h3> -<p>Pure iron is a chemical curiosity which looks -very much like silver. As obtained from its ores, -or as it occurs in Nature, iron always has some -impurities with it, such as carbon, silicon, sulphur -and phosphorus, and these are highest in the -crudest iron such as “pig-iron.” Its malleability -and ductility are only a little less than for gold -and silver, and so it has a wide range of qualities -for use by man. It is only rarely found native in -minute grains in some of the dark lavas. There -<span class="pb" id="Page_48">48</span> -is however one remarkable exception to this -statement, in that on Disco Island, Greenland, -there is a basaltic rock, from which are weathered -great boulders of native iron up to 20 tons in -weight. This iron is very like that occurring in -meteorites, and probably came from great depths -in the earth’s interior. The specific gravity of -iron is 7.8. It makes up around 5% of the crust -of the earth, and probably occurs in much larger -percentages in the interior of the earth.</p> -<p>Iron was discovered by man later than gold or -silver or copper, about 1000 <span class="small">B.C.</span>; but once found -it was so much more abundant than any of -these that it soon dominated over copper, and -from Roman times to the present has been the -basis of progress in civilization, and these times -are well called “the iron age.”</p> -<p>Iron unites freely with the non-metals, and -occurs as sulphides, oxides, carbonates, etc., and -is also present as a secondary metal in that -great group of minerals known as the silicates -(see <a href="#Page_97">page 97</a>). It alloys with a wide range of -other metals, every combination altering the -properties of the iron, and thus making it useful -in a still greater range of manufacture. The -introduction of ¼ to 2½% of carbon into iron -makes steel, which is harder (in proportion to the -amount of carbon) and stronger than the pure iron.</p> -<p>Iron compounds are among the most numerous -and important of the colors in Nature’s paint -box, limonite furnishing the browns which color -the soil and so many of the rocks, hematite giving -the red color to other abundant rocks, and -magnetite often coloring igneous rocks black, -<span class="pb" id="Page_49">49</span> -while the chlorophyll which gives the green -color to plants is an iron compound, as is also the -hemoglobin which gives the red to our blood.</p> -<p>Iron is present in all igneous rocks, and -secondarily in the sedimentary and metamorphic -rocks. It is soluble in water, and so is being -constantly transferred from place to place, and -changes from one compound to another, according -to the circumstances in which it is placed.</p> -<p>The primary forms are pyrite, magnetite and -the silicates. When in weathered rocks the iron -is changed to limonite, siderite or hydrated silicates. -Hematite is an intermediate oxide from -which the water contained in limonite has been -driven off by moderate heat or bacterial action.</p> -<h3><a id="species_Limonite">Limonite</a> -<br />2Fe₂O₃·3H₂O -<br /><a href="#Plate_12">Pl. 12</a></h3> -<p>Never crystalline, occurs in mammillary, -botryoidal and stalactitic -forms, or in fibrous, compact, oolitic, -nodular or earthly masses; hardness 5.5; specific -gravity 3.8; color yellow-brown to black; streak -yellow-brown; luster metallic to dull; opaque.</p> -<p>Limonite is a very common mineral, the color, -streak and hardness identifying it readily. Iron -rust is its most familiar form. When powdered -it is the ochre yellow used in paints. Being so -universally distributed, it is to be expected it will -occur in a variety of ways. First, there is the -fibrous type found lining cavities, in geodes, or -hanging in stalactites in caves. This has a -silky luster, an opalescent, glazed or black surface, -and is in mammillated or botryoidal masses. -Second, it may occur in compact masses in veins, -where it was deposited by waters; which, circulating -<span class="pb" id="Page_50">50</span> -through the adjacent rocks, gathered it -from the rocks, and, on reaching the open seams, -gave it up again. Third, it may occur in beds -on the bottom of ponds, where it was deposited -by waters which gathered it as they flowed over -the surface of the country rocks. Measurements -in Sweden show that it may accumulate in such -places as much as six inches in the course of -twenty years. In ponds and swamps, the decaying -vegetation forms organic compounds, which -cause the precipitation of the iron from the water, -as it is brought in by the streams. This sort of -iron in the bottom of ponds or swamps is also -known as “bog iron.” Another form in which -limonite may occur in ponds, lakes, or even the -sea, is in oolitic masses. In this case the iron -forms in tiny balls, with perhaps a grain of sand -at the center, and one coat of iron after another -formed around it, like the layers of an onion. If -the resulting balls are tiny this is called oolitic -(like fish eggs), but if the balls are larger it is -pisolitic (like peas). Bacteria probably have a -good deal to do with the precipitation of limonite -in this manner. Fourth, limonite occurs in -earthy masses, usually mixed with impurities -like clay and sand, which are the residue left -behind, where limestones have been dissolved by -weathering. The fifth mode of occurrence is -known as gossan, or “the iron hat,” which is a -mass of limonite capping a vein of some sulphide -mineral, like pyrite, chalcopyrite or pyrrhotite, -which has been exposed to weathering; and in -these minerals the sulphur has been removed, -leaving a mass of limonite over the vein. This is -<span class="pb" id="Page_51">51</span> -particularly common in the west. Limonite is -quite easily fusible and so was probably the -first ore from which early man extracted iron.</p> -<p>Limonite is iron oxide, with 3 molecules of -water of crystallization (or constitution) associated -with every 2 molecules of the oxide. If -limonite is moderately heated the water is -driven out and the resulting compound is hematite, -the same oxide, but without the water. In -this case and many other similar cases, as -gypsum, opal, etc., we have two or more minerals -resulting from the presence or absence of water -in the mineral. The water molecules have a -definite place in the arrangement of molecules -which determines the structure of the mineral. -Sometimes the water is driven out at a temperature -around 212 F., in which case it is called, -water of crystallization, but in other cases as -gypsum, a considerably higher temperature is -required to drive out the water, and then it is -called, water of constitution. In all cases the -removal of the water changes the arrangement of -molecules and a new mineral results, with -characteristics of its own.</p> -<p>In this case limonite is only one of a series of -minerals which have the Fe₂O₃ molecule as a -basis, and that incorporate more or less water -into their molecular construction as follows:</p> -<table class="center" summary=""> -<tr><td class="lbottom">Turgite </td><td class="lbottom">2Fe₂O₃·H₂O</td></tr> -<tr><td class="lbottom">Goethite </td><td class="lbottom">Fe₂O₃·H₂O</td></tr> -<tr><td class="lbottom">Limonite </td><td class="lbottom">2Fe₂O₃·3H₂O</td></tr> -<tr><td class="lbottom">Xanthosiderite </td><td class="lbottom">Fe₂O₃·2H₂O</td></tr> -<tr><td class="lbottom">Limonite </td><td class="lbottom">Fe₂O₃·3H₂O</td></tr> -</table> -<div class="pb" id="Page_52">52</div> -<p>Of these goethite is crystalline, the others non-crystalline. -They may occur pure or in all -sorts of mixtures, the mixtures usually being -lumped under limonite. The limonite is far -the commonest of the series, goethite is fairly -common, but the others are rare as pure -minerals.</p> -<p>Limonite is found in all parts of all states and -in every country. Though so common, it is by -no means an important source of iron today, -only about one percent of the iron mined in this -country coming from this source, though in Germany, -Sweden and Scotland it is relatively much -more important.</p> -<h3><a id="species_Goethite">Goethite</a> -<br />Fe₂O₃·H₂O -<br /><a href="#Plate_12">Pl. 12</a></h3> -<p>Occurs in lustrous brown to black -orthorhombic prisms, usually terminated -by low pyramids; hardness -5; specific gravity 4; color brown to black; streak -brownish-yellow; luster imperfect adamantine; -opaque.</p> -<p>Goethite, named for the poet Goethe, who was -interested in mineralogy, is much less abundant -than limonite or hematite, but occurs with -them, when they are in veins. Its usual form -is an orthorhombic prism with the edges beveled, -and a low pyramid on either end. The crystals -usually grow in clusters, making a fibrous mass, -often radiated, in which case it is known as -“needle iron stone”; or the prisms may be so -short as to be almost scales; when, because of the -yellowish-red color, it is called “ruby mica”. It -is found in many states, including Connecticut, -Michigan, Colorado, etc.</p> -<div class="pb" id="Page_53">53</div> -<h3><a id="species_Hematite">Hematite</a> -<br />Fe₂O₃ -<br />Pl. <a href="#Plate_13">13</a> & <a href="#Plate_14">14</a> -<br /><i>specular iron</i></h3> -<p>Occurs in compact, mammillary, -botryoidal, or stalactitic masses of -dark red to black color, or in earthy -masses of bright to dark red; hardness -6; specific gravity 5.2; color ochre red to -black; streak cherry red to dark red; luster -metallic, vitreous, or dull; opaque on thin edges.</p> -<p>Hematite is readily distinguished from other -red minerals by its hardness and streak. It may -occur in crystals, which belong to the hexagonal -system, and are usually hemihedral forms of the -double pyramid, or rhombohedrons. These -rhombohedrons usually have the edges beveled, -as in <a href="#Plate_13">Pl. 13</a>, A; or are tabular in form as a result -of the beveling of two of the opposite edges to -such an extent that a form like <a href="#Plate_13">Pl. 13</a> B results. -However the usual occurrence is in non-crystalline -masses, which represent transformations -from limonite by the loss of water of crystallization -on the part of the limonite. In such -cases we have fibrous, oolitic or compact masses, -according to the form in which the limonite -occurred. The transformation from limonite into -hematite involves some heat to drive out the -water of crystallization, but nothing like what is -involved in metamorphism.</p> -<p>Hematite is the source of 90% of the iron -mined in this country. Part of it comes from -the famous Clinton iron ore, a layer a foot or -more in thickness; starting in New York State, -and extending all down the Appalachian Mountains -to Alabama, where it is ten or more feet -thick and the basis of the Birmingham iron -industries. Then there are tremendous deposits -<span class="pb" id="Page_54">54</span> -of earthy to compact hematite, probably -derived from limonite, around the west end of -Lake Superior. This latter region yields today -around 75% of the iron for this country.</p> -<p>Loose earthy masses of hematite are often -known as “ochre red,” and were used by the -Indians for war paint. Today the same sort of -material is obtained by powdering hematite -and using it for red paint. The red color in -great stretches of rock is due to the presence of -small amounts of hematite, acting as cementing -material. The red of the ruby, garnet, spinel, -and the pink of feldspars and calcite are due to -traces of hematite.</p> -<p>This mineral is very common and found in -every state.</p> -<h3><a id="species_Magnetite">Magnetite</a> -<br />Fe₃O₄ -<br /><a href="#Plate_14">Pl. 14</a> -<br /><i>Magnetic iron ore</i></h3> -<p>Occurs in masses or in isometric -octahedrons or dodecahedrons; -hardness 6; specific gravity 5.8; -color black; streak black; luster -metallic; opaque on thin edges.</p> -<p>Magnetite is another important ore of iron, -and is peculiar in being strongly magnetic; its -name being derived, according to Pliny, from -that of the shepherd Magnes, who found his -iron pointed staff attracted by the mineral when -he was wandering on Mount Ida. This magnetic -property has been repeatedly used to locate -beds of magnetite, and is very helpful in separating -magnetite from the “black sands,” of which -it so often forms a part. These sands however -generally have magnetite with so much titanium -in it that they are unfit for smelting.</p> -<div class="pb" id="Page_55">55</div> -<p>Magnetite is found in association with igneous -or metamorphic rocks, and often represents -limonite or hematite which has been altered as -the result of high temperatures. Some of it, -in the igneous rocks especially, was undoubtedly -in the molten magma and has crystallized out -from the magma while it was still hot. It is the -form of iron always indicative of former high -temperatures. It is an ore mineral for about -3% of the iron in this country, but in Scandinavia -and some other countries, it plays a leading -role as the source of iron.</p> -<p>It is found in the Adirondack Mountains, in -New Jersey, Pennsylvania, Arkansas, North -Carolina, New Mexico, and California.</p> -<h3><a id="species_Siderite">Siderite</a> -<br />FeCO₃ -<br />Pl. <a href="#Plate_13">13</a> & <a href="#Plate_14">14</a> -<br /><i>Spathic iron</i></h3> -<p>Occurs in fibrous botryoidal -masses or rhombohedral crystals, -sometimes with curved faces; hardness -3.5; specific gravity 3.8; color -gray-brown; streak white; luster vitreous; translucent -on thin edges.</p> -<p>Like hematite this mineral belongs to the -hexagonal system, and crystallizes in hemihedral -form, making the rhombohedron. Its -faces are often curved, which is rare in minerals, -only a few forms like this and dolomite having -other than plane faces. When siderite crystals -grow in clusters, the crowding often results in -growth on one face only, making a mass of -fibrous character, and in such cases the surface -of the mass is botryoidal in contour. The -mineral is likely to oxidize, losing its gray-brown -color, and becoming limonite. In the United -<span class="pb" id="Page_56">56</span> -States it is scarcely ever used as an ore for iron, -but in Germany and England a great deal of iron -is smelted from this mineral.</p> -<p>It occurs in Massachusetts, Connecticut, New -York, throughout the Appalachian Mountains, -and also in Ohio.</p> -<h3><a id="species_Pyrite">Pyrite</a> -<br />FeS₂ -<br />Pl. <a href="#Page_15">15</a> & <a href="#Page_16">16</a> -<br /><i>iron pyrites</i></h3> -<p>Occurs as cubes, octahedrons and -pyritohedrons, or in compact masses, -scales or grains; hardness 6; specific -gravity 5.1; color brassy yellow; -streak greenish-black; luster metallic; opaque -on thin edges.</p> -<p>This is one of the commonest of all minerals. -It is found in all kinds of rocks, with all kinds -of associations, in all parts of the world. Its -crystals are isometric, and cubes and octahedrons -are abundant. The pyritohedron is also a common -form, and characteristic of this mineral. -It is a hemihedral form derived from a 24-sided -form, <i>i.e.</i> the cube with four faces on each -side. On this 24-sided form each alternate face -has developed and the others have disappeared, -resulting in a 12-sided form, known as the -pyritohedron, which differs from the dodecahedron -in that each of its faces is five-sided instead -of rhomboidal. When in crystals pyrite can not -be easily confused with any other mineral; but -when in masses it is often mistaken for gold, -chalcopyrite, pyrrhotite or marcasite. From -the first two, the color should be sufficient to -distinguish it, for they are golden yellow. -Pyrrhotite is bronze yellow, and marcasite is -paler yellow. Then too in hardness pyrite is -<span class="pb" id="Page_57">57</span> -much harder than any of these minerals except -marcasite. This last is the one which is most -likely to cause real difficulty. Its lighter color, -and the fact that it usually comes in fibrous -masses are the best distinctions.</p> -<p>In spite of being so abundant pyrite is scarcely -ever used as an ore for iron, because the sulphur -makes the metal “short,” or brittle, and the sulphur -is not easily gotten entirely out of the iron; -but pyrite is used largely in the manufacture of -sulphuric acid, so important to many of our -industries.</p> -<p>Other sulphides are commonly mixed with -pyrite, such as chalcopyrite, arsenopyrite, -argentite, etc.; but the most important impurity -is gold, which is often scattered through the -pyrite in invisible particles, and sometimes in -quantities enough to make it worth while to -smelt it for the gold.</p> -<p>Pyrite is particularly the form in which the -sulphur compounds of iron appear in rocks which -have been highly heated, and is to be expected in -metamorphic rocks and also igneous rocks, -especially in fissures and veins leading from the -igneous rocks. It may occur in sedimentary -rocks, but in these last it is usually marcasite.</p> -<h3><a id="species_Marcasite">Marcasite</a> -<br />FeS₂ -<br /><a href="#Plate_15">Pl. 15</a> -<br /><i>white pyrite</i></h3> -<p>Occurs in orthorhombic crystals, -usually grouped to make fibrous or -radiating masses, or non-crystalline -in masses; hardness 6; specific gravity -4.8; color pale brassy-yellow; streak greenish-gray; -luster metallic; opaque on thin edges.</p> -<p>Marcasite has the same chemical composition, -<span class="pb" id="Page_58">58</span> -as pyrite, and looks like it, but is lighter colored -and usually occurs in fibrous masses. It is the -commoner form in limestones and shales, while -pyrite is more likely to occur in igneous and -metamorphic rocks. It seems probable that -marcasite is due to a more hasty precipitation -from cold solutions, while pyrite is deposited -more slowly from hot solutions.</p> -<p>Isolated crystals of marcasite are rare; but, if -formed, they belong to the orthorhombic system. -Usually some form of twinning is present, and -because of the multiple character of the twinning, -marcasite crystals usually show a ragged outline, -with reentrant angles. It is most abundant -in radiated masses, which appear fibrous on the -broken surfaces. It decomposes easily, taking -oxygen from the air and forming, even in -museum cases, a white efflorescence or “flower,” -which is iron sulphate or melanterite. In moist -air it takes water and decomposes to sulphuric -acid which may change the surrounding limestone -to gypsum. Marcasite is found wherever -limestones and shales are the country rock.</p> -<h3><a id="species_Pyrrhotite">Pyrrhotite</a> -<br />Fe₁₁S₁₂ -<br /><i>Magnetic pyrites</i></h3> -<p>Occurs in masses; hardness 4; -specific gravity 4.6; color bronze; -streak grayish-black; luster metallic; -opaque on thin edges.</p> -<p>Tabular crystals are known, but are very rare. -They belong to the hexagonal system. This -form is easily distinguished from the other yellow -minerals by being magnetic. It is by no means -as abundant as the two preceding sulphides of -iron, but does occur fairly frequently in veins -<span class="pb" id="Page_59">59</span> -in igneous rocks, and less frequently in limestones, -large quantities of sulphuric acid being -made from a deposit in limestone at Ducktown, -Tenn. It will be found in most states. When -associated with nickel it is an important source -for the latter mineral, as at Sudbury, Canada. -Pyrrhotite is very like a substance found in -meteorites, known as troilite.</p> -<h3 class="center"><span class="sc">The Lead Group</span></h3> -<p>After learning how to get iron from the rocks -by rude smelting methods, the early peoples tried -heating various rocks, and some time around 500 -<span class="small">B.C.</span> stumbled upon lead, which is rather easily -separated from its ores. This metal was used -through Roman times to make pipes, gutters, etc.</p> -<p>Lead is a soft metal, fairly malleable, but with -little ductility, and still less tensile strength. -Though one of the commoner metals, it does not -occur as pure metal in Nature. It is diffused in -minute quantities through the igneous rocks, and -also is found in the sedimentary rocks and in -the sea water. Its minerals are few, galena, the -sulphide of lead, being the commonest, and at -the same time the form in which lead is primarily -deposited. Galena may also represent a secondary -deposition. The other minerals, cerrusite, -anglesite, and pyromorphite are results of modification -of the galena when it lies near enough to -the surface to be acted on by weathering agents, -like water and air. Lead minerals are usually -associated with zinc minerals, there being but few -places where the minerals of the one group occur -<span class="pb" id="Page_60">60</span> -without the other. Most lead when first smelted -from its ore, contains a greater or less amount of -silver in it, sometimes enough so that the lead ore -is better worth working for the silver than for the -lead.</p> -<p>Lead is used in making pipes, gutters, bullets, -etc., and in its oxide forms in the manufacture of -paints and glass. Eighty-three parts of lead -with 17 parts of antimony make type metal. -Lead and tin alloy to make solder. Lead and -tin with small amounts of copper, zinc and -antimony make pewter. The United States -produce about 20% of the world’s supply of this -metal.</p> -<h3><a id="species_Galena">Galena</a> -<br />PbS -<br /><a href="#Plate_17">Pl. 17</a> -<br /><i>lead glance</i></h3> -<p>Occurs in cubes or cleavable -masses; hardness 2.5; specific gravity -7.5; color lead-gray; streak lead-gray; -luster metallic; opaque.</p> -<p>While there is quite a group of lead-gray minerals, -galena is easily identified by its cleavage, -which is perfect in three directions parallel to -the cube faces. Even a moderate blow of the -hammer will shatter a mass of galena into small -cubic pieces. The crystals often have the corners -cut by octahedral faces, and occasionally the -edges are beveled by dodecahedral faces. It is -not uncommon to find crystals of large size, -several inches across. If galena has 1 to 2% of -bismuth as an impurity, curiously enough, the -cleavage changes to octahedral, but this is a rare -occurrence.</p> -<p>Galena may occur as a primary mineral in veins -associated with igneous intrusions, or in irregular -<span class="pb" id="Page_61">61</span> -masses in metamorphic rocks; but it is more often -found in irregular masses in limestones, where the -limestone has been dissolved, and the cavities -thus formed, filled with secondary deposits of -galena. It also occurs at the contact between -igneous rocks and the adjacent rock, whatever -this may be. Sometimes it is found in residual -clays.</p> -<p>Among the most important lead deposits are -the Cœur d’Alene district in Idaho, where -galena with a high percentage of silver is mined; -the Leadville, Colo., district where lead, silver -and gold occur together in veins; the Joplin, -Mo., district, where lead and zinc ores occur -together in irregular masses in limestones; and -the Wisconsin district of similar character.</p> -<p>When found galena is usually associated with -sphalerite, argentite chalcopyrite, pyrite and -calcite. It will be found in every state.</p> -<h3><a id="species_Cerrusite">Cerrusite</a> -<br />PbCO₃ -<br /><a href="#Plate_18">Pl. 18</a> -<br /><i>White lead ore</i></h3> -<p>Occurs in fibrous or compact -masses, or in orthorhombic crystals, -usually on galena; hardness 3.5; -specific gravity 6.5; colorless; streak -white; luster adamantine; transparent on thin -edges.</p> -<p>While the crystals of this mineral simulate -hexagonal, they are actually orthorhombic, the -simple form being an octahedron with two of its -edges beveled, making double six-sided pyramids -(see <a href="#Plate_18">Pl. 18</a> A.) Usually prism faces are present. -Twinning is common, both the simple contact -sort, as shown on <a href="#Plate_18">Plate 18</a> B, and also the sort -in which three crystals have grown through each -<span class="pb" id="Page_62">62</span> -other, so as to make a six-rayed crystal. The -considerable weight, and the fact that it -effervesces in acid serve to identify cerrusite. -When pure it is colorless, but impurities cause it -to appear white, gray or grayish-black, and -sometimes it has a tinge of blue or green.</p> -<p>It is likely to occur wherever galena is found, -as a secondary mineral derived from the galena. -In this country it is not used as an ore, for, as in -the Leadville district, veins which have cerrusite -near the surface change at moderate depths, and -galena takes the place of the cerrusite. It is -found all down the Appalachian Mountains, and -in all the Cordilleran States. Especially fine -specimens have come from the Cœur d’Alene -district in Idaho.</p> -<h3><a id="species_Anglesite">Anglesite</a> -<br />PbSO₄ -<br /><a href="#Plate_18">Pl. 18</a></h3> -<p>Occurs in grains and masses, or in -tabular and prismatic orthorhombic -crystals; hardness 3; specific gravity -6.3; colorless; luster adamantine; transparent on -thin edges.</p> -<p>Two modes of occurrence are characteristic, -one in cavities in galena, the other in concentric -layers around a nucleus of galena. In the former -case fine crystals are developed, in the latter the -mineral is in masses. The crystals look like -those of barite, but are soluble in nitric acid -while the barite is insoluble. Sometimes the -crystals are prismatic with pyramidal faces -instead of the tabular form.</p> -<p>It is found in the lead mines associated with -galena, and in this country is not used as an ore -for lead, but in Mexico and Australia it is -<span class="pb" id="Page_63">63</span> -abundant enough to be mined as an ore. Exposed -to water which has carbon dioxide in it, -and most surface waters have some, it readily -changes to cerrusite. It is found in Missouri, -Wisconsin, Kansas, Colorado, and Mexico.</p> -<h3><a id="species_Pyromorphite">Pyromorphite</a> -<br />Pb₅Cl(PO₄)₃ -<br /><a href="#Plate_17">Pl. 17</a> -<br /><i>Green lead ore</i></h3> -<p>Occurs in small barrel-shaped -hexagonal crystals, and in fibrous or -earthly masses; hardness 3.5; specific -gravity 7; color green to brown; -luster resinous; translucent on thin edges.</p> -<p>Pyromorphite is found in the upper levels of -lead mines, and is formed by the decomposition -of galena. Its green color (sometimes shading -off toward brown), considerable weight and -resinous luster, serve to distinguish this mineral. -The crystal form is that of a simple hexagonal -prism, with the ends truncated. It is found in -Phœnixville, Penn., Missouri, Wisconsin, Colorado, -New Mexico, etc.</p> -<h3 class="center"><span class="sc">The Zinc Group</span></h3> -<p>Zinc and copper made the brass of early -Roman times; but even then, zinc was not known -as a separate metal, the brass being made by -smelting rocks in which both zinc and copper -occurred, the zinc never being isolated until -much later. Some time in the later Roman -times it seems to have been obtained separately, -but then and all down through the Middle Ages -zinc and bismuth were confused. Our earliest -record of zinc being smelted, as we know it today, -was about 1730 in England. In those earlier -<span class="pb" id="Page_64">64</span> -days, the product, zinc, or bismuth, or both -together, were known as “spelter,” and this -name has clung to zinc in mining and commercial -circles; so that today, if one looks for quotations -in the newspaper, he often finds zinc under the -head of spelter.</p> -<p>Zinc, like lead, is diffused in small quantities -through all the igneous rocks. In places it is -segregated in fissures or veins leading from the -igneous rocks, along the contact between igneous -rocks and either sedimentary or metamorphic -rocks, in limestones where solution cavities have -been formed and later filled with zinc minerals, -and as a residue where limestones have been -weathered away. In all these places it is closely -associated with lead.</p> -<p>The sulphide, sphalerite, is the primary -mineral, and the other minerals, like zincite, -smithsonite, calamine, willemite, franklinite, etc., -are secondary, resulting from modifications of -the original sphalerite. In connection with zinc -minerals the region of Franklin Furnace, N. J., -is especially interesting, for at that place are -found two large metamorphosed deposits containing -a wide range of zinc minerals, several of -which are not found anywhere else.</p> -<p>Zinc is soft and malleable, but is only slightly -ductile, and has little tensile strength. It alloys -with several metals, and in this form is most -useful today; three parts of copper to one of -zinc making brass; four or more parts of copper -and one of zinc, making “gold foil”; copper and -zinc (a little more zinc than copper) making -“white metal”; three parts of copper to one of -<span class="pb" id="Page_65">65</span> -zinc and one of nickel making German silver; -etc. Zinc is also used in large quantities in -galvanizing iron, sheets of iron being dipped -into melted zinc and thus thinly coated. It is -also used in batteries and a wide range of chemical -industries.</p> -<h3><a id="species_Sphalerite">Sphalerite</a> -<br />ZnS -<br />Pl. <a href="#Page_19">19</a> & <a href="#Page_20">20</a> -<br /><i>zinc blende, black jack</i></h3> -<p>Occurs in grains, in fibrous or -layered masses, or in isometric crystals; -hardness 3.5; specific gravity -4; color yellow-brown to almost -black; streak light yellow to brownish; -luster resinous to adamantine; translucent -on thin edges.</p> -<p>When in crystals sphalerite occurs most commonly -either in dodecahedrons or in tetrahedrons -(hemihedral forms of the isometric octahedron). -The cleavage is fairly good and parallel to the -faces of the dodecahedron. The difficulty -usually is to get large enough crystalline masses -to see this cleavage clearly, but by examining -the angles between the faces of cleavage pieces -they will be found to be the same as those on a -dodecahedron. When the mineral is pure, it has -the color of resin, but sometimes it is reddish -to red-brown, and then it is called “ruby zinc,” -more often it is dark brown due to the presence of -iron as an impurity. This is what the miners -call “black-jack.” The presence of iron also -tends to make the streak darker. The hardness, -streak and cleavage will usually determine this -mineral readily.</p> -<p>Sphalerite is the primary ore of zinc and is -usually found in fissures and veins leading from -<span class="pb" id="Page_66">66</span> -masses of igneous rocks, or along the surface of -contact where igneous rocks like granite or lavas -come against such metamorphic rocks as gneisses, -schists, or crystalline limestones. In the -region of Joplin, Mo., however, the sphalerite is -of secondary character, having been gathered by -waters circulating through the limestones, and -deposited in them in irregular pockets. This -Joplin district has produced more zinc than any -other in the world. The United States annually -produces about 25% of the world’s supply of this -metal.</p> -<p>Sphalerite is always associated with galena, -and such other minerals as argentite, pyrite, -chalcopyrite, fluorite, quartz, calcite and barite, -are very apt to be present. It will be found in -almost every state, especially in fissures and -veins, and less frequently in cavities in limestones.</p> -<h3><a id="species_Zincite">Zincite</a> -<br />ZnO -<br />Pl. <a href="#Page_19">19</a> & <a href="#Page_20">20</a> -<br /><i>red zinc ore</i></h3> -<p>Usually occurs massive, but may -be found in crystals; hardness 4; -specific gravity 5.6; color deep red; -streak orange; luster subadamantine; -translucent on thin edges.</p> -<p>When in crystals zincite forms in hexagonal -prisms with hexagonal pyramids on the ends. -This is rather rare, most of the zincite being -found in massive form. The cleavage is parallel -to the prism faces and perfect. The deep red -color and orange streak are wholly -characteristic.</p> -<p>This mineral is so common at Franklin Furnace, -N. J., as to be an important ore, but it is -very seldom found elsewhere. This district, as -<span class="pb" id="Page_67">67</span> -mentioned before, is a peculiar one for zinc -minerals. The zinc beds are in a metamorphosed -limestone, and into this are intruded -numerous dikes of granite. Probably the zinc -was originally present in the bed of limestone -as smithsonite, calamine and other secondary -minerals of zinc. When intruded by the hot -granite the smithsonite (carbonate) may well -have been altered to the oxide, zincite; while the -calamine (hydrous silicate) became the simple -silicate, willemite.</p> -<h3><a id="species_Willemite">Willemite</a> -<br />ZnSiO₄ -<br /><a href="#Plate_20">Pl. 20</a></h3> -<p>Occurs in masses or in crystals; -hardness 5.5; specific gravity 4.1; -color pale yellow when pure; luster -resinous; translucent on thin edges.</p> -<p>Willemite is another of the minerals which are -distinctively characteristic of Franklin Furnace, -and found elsewhere very rarely. It is so common -there as to be one of the principal ores, and -mostly occurs in irregular masses, but is also -found in crystals. These are hexagonal prisms, -with a three-sided (rhombohedral) pyramid on -the ends. The color when pure is whitish or -greenish-yellow, but with small amounts of -impurities it may be flesh-red, grayish-white or -yellowish-brown. When in crystals it is easily -determined; but when massive it looks like -calamine, and can only be distinguished by placing -a bit of the mineral in a closed tube and -heating it, in which case calamine will give off -water vapor, while willemite will not.</p> -<p>This mineral is one of those resulting from -metamorphic alteration and is derived from -<span class="pb" id="Page_68">68</span> -calamine, when the latter loses its water of -crystallization. It is common at Franklin -Furnace, N. J., and also found occasionally -elsewhere, as at Salida, Colo., and in Socorro Co., -New Mexico.</p> -<h3><a id="species_Calamine">Calamine</a> -<br />Zn₂(OH)₂·SiO₃</h3> -<p>Occurs as crystalline linings in -cavities, or as botryoidal or stalactitic -masses; hardness 5; specific gravity 3.4; colorless -to white; luster vitreous.</p> -<p>Calamine resembles both smithsonite and -willemite when in non-crystalline masses. From -the smithsonite it is easily separated by the -fact that in nitric acid the smithsonite effervesces -and the calamine does not. From willemite it is -harder to distinguish, but a piece may be placed -in a closed tube and heated. If it is calamine -water vapor will be given off, if willemite nothing -happens. When calamine occurs in crystals -these are orthorhombic and mostly tabular, and -the crystals are peculiar in that the two ends are -terminated differently.</p> -<p>Both this and smithsonite are secondary -minerals and usually occur together when zinc is -found in limestones. It is abundant at Franklin -Furnace and Sterling Hill, N. J., and also found -at Phœnixville, Penn., in Wythe Co., Va., and -Granby, Mo.</p> -<h3><a id="species_Smithsonite">Smithsonite</a> -<br />ZnCO₃ -<br /><a href="#Plate_21">Pl. 21</a> -<br /><i>Dry bone</i></h3> -<p>Usually occurs as incrustations, -grains, earthy or compact masses, -and as crystals; hardness 5; specific -gravity 4.4; color white, yellow, -greenish or bluish; streak white; luster vitreous; -transparent on thin edges.</p> -<div class="pb" id="Page_69">69</div> -<p>When pure this mineral is colorless, but, as it -occurs, it is usually white, or tinged with some -shade of yellow, green, or blue, but in all cases its -streak is white. The crystals are rhombohedrons -often with edges beveled or corners cut by other -faces. It resembles calamine and willemite, but -is readily separated from either of these by the -acid test, for smithsonite effervesces when acid -is placed on it.</p> -<p>Next to sphalerite, smithsonite is the commonest -of the zinc minerals. It is a secondary -mineral, resulting from the action of lime-charged -water acting on sphalerite, and so is -likely to be found wherever zinc minerals occur -in a limestone region. In the Wisconsin-Illinois-Iowa -district it serves as a minor ore of zinc, and -is termed here “dry bone.” It is also found in -the Missouri and Arkansas districts, and in -Europe is an important ore for zinc.</p> -<h3><a id="species_Franklinite">Franklinite</a> -<br />(ZnMn)Fe₂O₄ -<br /><a href="#Plate_21">Pl. 21</a></h3> -<p>Occurs in compact grains or -masses, and in isometric octahedrons; -hardness 6; specific gravity -5; color black; streak reddish-brown; luster -metallic; opaque on thin edges.</p> -<p>This is a mineral peculiar to the Franklin Furnace -region, from which it gets its name. It -looks like magnetite, but its reddish-brown -streak and lack of magnetism distinguish it. -When it occurs in octahedrons, the edges are -rounded, while those of magnetite are sharp. It -is a complex and variable oxide of zinc, iron and -manganese, which has resulted from the metamorphism -of the beds in which it occurred -<span class="pb" id="Page_70">70</span> -probably being originally something quite -different.</p> -<h3 class="center"><span class="sc">The Manganese Group</span></h3> -<p>Though manganese was known in the mineral -pyrolusite in early times, it was then thought to -be magnetite or magnetic iron ore. It was not -until 1774 that it was isolated and recognized -as a distinct element.</p> -<p>Manganese is one of the lesser elements in the -crust of the earth, making less than .07 of one -percent, but as an alloy with other metals, -especially iron, it has attained a considerable -importance to man. It is used chiefly with iron, -20% of manganese making the alloy, spiegeleisen, -a combination which occurs in Nature in Germany, -and from 20% to 80% making ferromanganese. -These alloys are in great demand -because they make an especially tough steel essential -in the manufacture of munitions. The -sources for manganese are the oxide ores, manganite, -pyrolusite and psilomelane, which have -been formed as secondary minerals, as a result of -the weathering of silicates which carry manganese. -They occur widely enough, but throughout -the United States the deposits are small, and this -is one of the elements in which this country is not -self-sufficient. The largest producer of manganese -is Russia; however she consumes almost all of her -output at home, and our supply comes from the -next largest producers, India, the Union of South -Africa, and the Gold Coast. A shift in trade may -be expected when Brazil’s recently discovered ore -body in Matto Grosso is brought into full production. -<span class="pb" id="Page_71">71</span> -Besides being used as an alloy, manganese is -employed in making paints and dyes, for clearing -glass, and for some types of electric batteries.</p> -<h3><a id="species_Pyrolusite">Pyrolusite</a> -<br />MnO₂</h3> -<p>Occurs in earthy or fibrous masses; -hardness 1-2; specific gravity 4.8; -color black; streak black; luster -dull; opaque.</p> -<p>Pyrolusite occurs in soft masses and incrustations, -usually leaving a sooty mark on the fingers. -Sometimes it seems to be in crystals, but these -are pseudomorphs which have the form of manganite, -from which the pyrolusite has formed as a -result of the water having been driven from the -manganite. Frequently pyromorphite and manganite -will be found together, and in some cases -the outer part of a mass or crystal will be pyrolusite, -while the center is still manganite. Psilomelane -is another oxide of manganese with -water and may appear very like pyrolusite, but -both manganite and psilomelane have much -greater hardness than does pyrolusite. If there -is difficulty in deciding about pyrolusite, it may -be placed in a closed tube and heated. It will -not be affected by the heat, while, under the -same circumstances, both manganite and psilomelane -will give off water vapor.</p> -<p>Pyrolusite usually occurs in black streaks or -pockets in residual clays which have formed as a -result of the decomposition of limestones. It -may also occur in dendritic forms in seams and -crevices (see manganite). It is found in Vermont, -Massachusetts, Virginia, Arkansas, Colorado, -California, etc.</p> -<div class="pb" id="Page_72">72</div> -<h3><a id="species_Psilomelane">Psilomelane</a> -<br />MnO₂·H₂O</h3> -<p>Occurs in compact botryoidal or -stalactitic masses; hardness 5-6; -specific gravity 4.2; color black; -streak brownish-black; luster metallic; opaque -on thin edges.</p> -<p>Psilomelane is very like pyrolusite, and often -occurs with it. It is distinguished by its greater -hardness, and the fact, that when heated in a -closed tube, it gives off water vapor. From -manganite it is more easily distinguished, for it -never occurs in crystals, while the manganite is -usually crystalline. This and pyrolusite are the -principal ores of manganese.</p> -<p>Wad is an impure form of psilomelane, having -some iron oxide mixed with the manganese oxide, -usually limonite; or the impurity may take the -form of a copper, cobalt, lithium or barium -oxide.</p> -<p>Psilomelane is found at Brandon, Vt., in -Arkansas, Colorado, California, etc.</p> -<h3><a id="species_Manganite">Manganite</a> -<br />Mn₂O₃·H₂O -<br /><a href="#Plate_22">Pl. 22</a></h3> -<p>Occurs in prismatic crystals, or in -columnar or fibrous masses; hardness -4; specific gravity 4.4; color -steel gray; streak reddish-black; luster submetallic; -opaque on thin edges.</p> -<p>This is the form taken by manganese oxide -when it crystallizes in the presence of moisture, -and pyrolusite frequently changes to manganite -when exposed to moisture. The crystals are -orthorhombic prisms, with striated sides and the -ends truncated. These prisms usually occur in -bundles and give the mineral a fibrous appearance. -Manganite is not hard to identify, the -<span class="pb" id="Page_73">73</span> -striations on the crystals and the streak being -very characteristic.</p> -<p>In seams and tiny crevices this mineral, and -often pyrolusite, grows in a branching manner, -resembling tree-like or “mossy” masses. This is -termed dendritic, and the growths of manganese -minerals are called dendrites. One of the most -curious of these is when the “mossy” growth is -inclosed in chalcedony, making the so-called <i>moss -agate</i>. These moss agates are abundant through -the Rocky Mountains and are frequently cut for -semi-precious stones. The finest ones however -come from India and China.</p> -<p>Manganite is found in the Lake Superior -region, Colorado, etc.</p> -<h3><a id="species_Rhodochrosite">Rhodochrosite</a> -<br />MnCO₃</h3> -<p>Occurs in compact cleavable -masses; hardness 4; specific gravity -3.5; color rose to dark red; streak -white; luster vitreous; translucent on thin edges.</p> -<p>This usually occurs in pink to red masses which -cleave readily parallel to the faces of the rhombohedron. -When it is found in crystals, which -are rare, these too are rhombohedrons. It is -usually found in veins as a gangue mineral with -copper, silver or zinc ores. Its beautiful color and -the fact that it effervesces in acid serve to distinguish -this mineral. It is found at Branchville, -Conn., at Franklin Furnace, N. J., and in veins -with silver in Colorado, Nevada, and Montana.</p> -<h3 class="center"><span class="sc">The Aluminum Group</span></h3> -<p>Though aluminum is one of the most abundant -of all the metals, making some 8% of the crust of -<span class="pb" id="Page_74">74</span> -the earth, its union with other elements is so -firm, that only recently have methods been -found for getting the metal free. It was first -isolated in 1846, but up to 1890 the extraction of -aluminum was so expensive, that it could not be -widely used. About that time electrical processes -were applied to its extraction, and since then the -price has steadily dropped, until now it is under -$.20 per pound. It is very malleable, and ductile, -and has high tensile strength. Exposed to -the air, water or ordinary gases, it does not -tarnish; and it is very light, an equal bulk weighing -about a third as much as iron. The combination -of lightness and strength, and the fact -that it is a good conductor of electricity, have -made it available for a wide range of uses, such -as electrical apparatus, delicate instruments, -boats, aeroplanes, and domestic utensils.</p> -<p>It is an essential component of all the important -rocks, except sandstone and limestone, and -combines to a greater or less degree in a host of -minerals. Though present in clays, shales, -argillites, feldspars, and micas, it is only from -bauxite that it has been successfully extracted. -Aside from the small number of simple compounds -of aluminum grouped here, it also takes -a part in the make-up of a large series of minerals -termed silicates, treated a little further on in -this book.</p> -<p>It alloys with other metals, especially copper. -The union of copper and a small amount of -aluminum makes aluminum-bronze, which looks -like gold and is used for watch chains, pencil-cases, -etc., and also for the antifriction bearings -<span class="pb" id="Page_75">75</span> -of heavy machinery. A small amount added to -steel prevents air holes and cracks in casting.</p> -<h3><a id="species_Corundum">Corundum</a> -<br />Al₂O₃ -<br /><a href="#Plate_23">Pl. 23</a></h3> -<p>Occurs in cleavable masses or in -hexagonal crystals; hardness 9; -specific gravity 4; colorless, red, -yellow, blue, or gray; luster vitreous to adamantine; -translucent to transparent on thin -edges.</p> -<p>Corundum is readily recognized by its hardness, -second only to that of the diamond. The -crystals may be simple six-sided prisms, hexagonal -pyramids or combinations of the two. -The cleavage is usually described as parting, for -it is by no means perfect, but when it is recognizable -it is parallel to the faces of a rhombohedron, -and cleavage pieces may appear almost cubic.</p> -<p>When in clear and perfect crystals this mineral -is one of the most highly prized of all the gems. -Clear and colorless it is known as the “<i>Oriental -white sapphire</i>”; when tinged with blue it is the -<i>sapphire</i>; when colored yellow, the “<i>Oriental -topaz</i>”; when green, the “<i>Oriental emerald</i>”; -when purple, the “<i>Oriental amethyst</i>” and when -red, the <i>ruby</i>. Sapphires range from colorless -to deep blue, the value depending on the shade -of the blue, and increasing as the color deepens. -The Oriental topaz can easily be confused with -the true topaz, which is a much commoner and -less valuable gem, but can be distinguished by -the hardness, topaz having a hardness of but 8. -The name emerald is applied to several green -gems, mostly to beryl, which is not so hard and -is the true emerald. The Oriental emeralds have -<span class="pb" id="Page_76">76</span> -a value about the same as diamonds. Rubies of -clear and deep color are the rarest of all gems, -ranging in value about three times as high as -diamonds of equal size. The most sought-for -shade is the so-called “pigeon-blood red,” and -the value of a stone of this sort is almost dependent -on the whim of the buyer. The best of -the rubies come from granites or metamorphosed -limestones in Burma; the best sapphires from -Ceylon, though both of these, and some of the -other corundums of gem quality, have been -found in North Carolina and Montana.</p> -<p>Around these stones, which have been used so -long among the Hindus, Persians, Jews, Egyptians, -and Christians, a wealth of lore has been -woven. The sapphire was Saturn’s stone, and a -talisman to attract Divine favor. Where tradition -makes the stone on which the ten commandments -were written the sapphire, it is probable -that, what was really meant, is lapis lazuli, -as is also the case when sapphires are mentioned -as building stones for the celestial gates. The -ruby in ancient lore is termed “lord of stones,” -“gem of gems” etc., and so protected its wearer -that he was safe from injury in peace or war.</p> -<p>When corundum is colored brown by impurities -of iron, it is termed <i>corundum</i>, when black -by greater quantities of iron, it is <i>emery</i>. These -varieties are far the commonest form in which -corundum occurs, and when ground to finer or -coarser powder make the commercial emery. -Emery is likely to be found in sands, making so-called -“black sands,” where it has accumulated -as a result of the weathering to bits corundum-bearing -<span class="pb" id="Page_77">77</span> -rocks. In some one of its forms, corundum -is found in Massachusetts, Connecticut, -New York, New Jersey, and all down the Appalachian -Mountains, also in Colorado, Montana, -California, etc.</p> -<h3><a id="species_Bauxite">Bauxite</a> -<br />Al₂O₃·2H₂O</h3> -<p>Occurs in grains, or oolitic or -clay-like masses; hardness 1-3; specific -gravity 2.5; color white to yellowish-white -or reddish-brown.</p> -<p>Bauxite never comes in crystals, but is usually -in earthy masses, which have resulted from the -decomposition of granitic or volcanic rocks, in -circumstances where hot alkaline waters were -present. This explanation seems to apply -especially to the deposits in France, which were -first the chief source of the bauxite, and may be -applicable to those in Georgia and Alabama. -Some of the other deposits, however, do not -seem to have had any hot water available, and -the deposit appears more like simple decomposition -of the underlying rocks by alkaline -waters.</p> -<p>In many cases bauxite resembles limonite in -being a mixture of two or more aluminum oxides -with water of crystallization, such as Al₂O₃·H₂O, -Al₂O₃·2H₂O and Al₂O₃·3H₂O. This is particularly -true of the bauxite which resulted from -the decomposition of rocks by surface water.</p> -<p>Bauxite is the ore from which aluminum is -obtained. The deposits are not large, but the -United States has its share of them. It is found -in Alabama, Arkansas, Georgia, Missouri, Tennessee, -and California.</p> -<div class="pb" id="Page_78">78</div> -<h3><a id="species_Cryolite">Cryolite</a> -<br />Na₃AlF₆ -<br /><i>Ice stone</i></h3> -<p>Occurs in pseudo-cubic crystals or -massive; hardness 2.5; specific gravity -3; color white; luster vitreous; -transparent on thin edges.</p> -<p>Cryolite is a relatively soft mineral, colorless -to white as snow; for which reason, and partly -also because it comes mostly from Greenland -it is called “ice stone.” It is really monoclinic -but the inclination of the c axis is so slight, that, -unless examined carefully, the crystals appear -to be cubic. Until about 1900 great quantities -of this mineral were shipped from West Greenland, -and from them the metal aluminum was -extracted. When bauxite was discovered, it was -found to be considerably cheaper to make the -aluminum from that mineral, and now cryolite -is no longer sought. Aside from its occurrence -in Greenland some cryolite is found in Colorado, -near Pike’s Peak.</p> -<h3 class="center"><span class="sc">The Arsenic Group</span></h3> -<p>The metal, arsenic, is a dark steel gray in -color, when the surface is fresh, but it soon tarnishes. -It is very brittle and easily powdered -under the hammer, and its only use as a metal, -is for an alloy with lead in making shot. Its -compounds find a wider use. The white powder -called “arsenic” is arsenous acid, and is used -mostly in making poisons, which fortunately -are easily detected in animal tissues. Copper -arsenate, (<i>Scheele’s green</i>) is a pigment used in -making green paint, and formerly in the green -colors of wall paper. A combination of arsenous -acid, copper oxide and acetic acid is the well -<span class="pb" id="Page_79">79</span> -known <i>Paris Green</i>, so much used for an insecticide. -Beside these uses, arsenic serves a large -number of other purposes, as in making glass -and enamel, embalming fluids, and various -medicines.</p> -<p>Curiously arsenic plays a double part, acting -part of the time as a metal, as in the two following -minerals, and part of the time as a non-metal, -as in cobaltite, niccolite, etc.</p> -<h3><a id="species_Arsenopyrite">Arsenopyrite</a> -<br />FeAsS -<br /><a href="#Plate_24">Pl. 24</a></h3> -<p>Occurs in well formed crystals, -grains, or masses; hardness 5.5; -specific gravity 6; color silver-white; -streak black; luster metallic; opaque on thin edges.</p> -<p>When in crystals, they are usually short prisms -of the orthorhombic system, either end being -terminated with a low roof. Though usually -described as silver-white in color, there is always -a brassy cast to the color. Its appearance is -much like cobaltite and smaltite, but it can be -easily distinguished from both these by putting -a piece in nitric acid. The arsenopyrite will not -materially change the color of the fluid, but the -other two turn it rose-red, and all give off the -smell of sulphur. It looks sometimes like marcasite, -but that is yellower, and has the fibrous -structure, not found in arsenopyrite.</p> -<p>It is found in veins or in metamorphic rocks, -associated with argentite, galena, sphalerite, -chalcopyrite and pyrite. It is distinctly a -mineral formed by deposition from hot vapors or -hot water rising from either lavas, or in the -course of metamorphism.</p> -<p>It is found in New Hampshire, Vermont, -<span class="pb" id="Page_80">80</span> -Massachusetts, Connecticut, New York, New -Jersey, California, etc.</p> -<h3><a id="species_Realgar">Realgar</a> -<br />AsS -<br /><a href="#Plate_24">Pl. 24</a></h3> -<p>Occurs in incrustations or scattered -grains; hardness 1.5 to 2; specific -gravity 3.5; color orange; streak -orange; luster resinous; opaque on thin edges.</p> -<p>Crystals are very rare, but when found are -short monoclinic prisms. The color is aurora-red, -changing to orange as soon as it is exposed -to the air. This and the streak are entirely -characteristic. It is a mineral associated with -hot vapors or hot waters, and is found about -volcanoes, as deposits from the hot water of the -geysers in Norris Basin, Yellowstone Park, and -in veins, associated with barite, stibnite, quartz, -etc., as in Massachusetts, Utah, California, etc.</p> -<h3><a id="species_Orpiment">Orpiment</a> -<br />As₂S₃</h3> -<p>Occurs as incrustations or -powdery masses; hardness 1 to 2; -specific gravity 3.5; color lemon -yellow; streak yellow; luster resinous.</p> -<p>This mineral is very like realgar in its physical -properties, and likely to occur with it. It gives -the lemon yellow color to the basins about hot -springs, as in the Yellowstone Park, and about -volcanoes. It also comes in veins with realgar.</p> -<h3 class="center"><span class="sc">Molybdenum</span></h3> -<p>Molybdenum is a rare metal, silvery-white in -color, brittle and very difficult to fuse. It is used -mostly as an alloy of steel, to make certain -grades of tool steel. The world’s greatest supply -is obtained from Climax, Colorado, where the -principal ore mineral is molybdenite.</p> -<div class="pb" id="Page_81">81</div> -<h3><a id="species_Molybdenite">Molybdenite</a> -<br />MoS₂</h3> -<p>Occurs in scales or scaly masses, -occasionally in tabular hexagonal -crystals; hardness 1.5; specific gravity -4.7; color lead-gray; streak bluish-gray; -luster metallic; opaque.</p> -<p>This mineral is the chief source for the metal -molybdenum. Its extreme softness and greasy -feel will distinguish it at once from any other -mineral except graphite, which has much the -same qualities, but its scaly character and the -more bluish tinge in streak and color will distinguish -these two.</p> -<p>It occurs in granites, gneisses, and metamorphic -rocks in Colorado, New Mexico, Maine, -Connecticut, New Hampshire, New York, Pennsylvania, -etc.</p> -<h3 class="center"><span class="sc">Antimony</span></h3> -<p>Antimony is another hard, brittle metal, of -bluish-white color. Exposed to the air at ordinary -temperatures it does not tarnish; and this -combined with its hardness make it useful for -such alloys as Britannia metal, type metal, and -pewter. Only one of its minerals, stibnite, is -common enough for mention.</p> -<h3><a id="species_Stibnite">Stibnite</a> -<br />Sb₂S₃ -<br /><a href="#Plate_25">Pl. 25</a> -<br /><i>gray antimony</i></h3> -<p>Occurs in prismatic or needle-like -crystals; hardness 2; specific gravity -4.5; color lead-gray; streak lead-gray; -luster metallic; opaque.</p> -<p>The crystals of stibnite are orthorhombic -and usually elongated, -the sides striated and the ends with low pyramids -<span class="pb" id="Page_82">82</span> -on them. Sometimes the long crystals are -curved or even twisted. There is a well-developed -cleavage parallel to face b in the figure. -While the color is similar to that of galena, the -form and cleavage are so different that stibnite -is easily determined.</p> -<p>The ancients used stibnite to color their eyebrows, -now it is the source for the metal antimony. -Hungary and Japan are famous for the -fine large crystals they produce; but moderate -sized crystals may be found in this country. It -occurs in veins along with pyrite, galena, cinnabar, -and realgar, with quartz, calcite or barite -as gangue minerals.</p> -<p>Stibnite has been found in Arkansas, California, -Nevada, and Utah.</p> -<h3 class="center"><span class="sc">The Nickel Group</span></h3> -<p>Nickel as a metal is silvery-white in color, -rather hard, and does not tarnish when exposed -to the air. When pure it is malleable and fairly -ductile. It is highly useful for plating other -metals to protect their surfaces. Alloyed with -steel, it makes a product of extreme hardness. -Copper, zinc, and nickel make the well known -German silver.</p> -<p>Nickel has a fairly large range of minerals, -but they do not occur with any abundance in -the United States, so that we have to import -most all of our nickel. In the earlier days New -Caledonia produced most of the world’s supply, -but recently since the finding of large nickel -deposits near Sudbury, Canada, this locality has -<span class="pb" id="Page_83">83</span> -not only outstripped New Caledonia, but now -produces four-fifths of the world’s supply. In -this country but two nickel minerals will be -found at all common.</p> -<h3><a id="species_Niccolite">Niccolite</a> -<br />NiAs -<br /><a href="#Plate_25">Pl. 25</a> -<br /><i>copper nickel</i></h3> -<p>Occurs in masses; hardness 5.5; -specific gravity 7.4; color pale coppery-yellow; -streak pale brownish-black; -luster metallic; opaque on thin edges.</p> -<p>Niccolite is very seldom in crystals, but if -they do occur they are hexagonal. The mineral -looks a little like smaltite, but in case there is -any question of the determination, dissolve a -piece in nitric acid, and if niccolite, it will color -the solution green.</p> -<p>Niccolite is usually associated with copper -and silver ores, and in this country has been -found at Chatham, Conn., and Silver Cliff, -Colo. It may be associated with pentlandite, a -sulphide of iron and nickel, which is similar in -appearance, but not so hard, and occurs in small -grains throughout dark lavas. The particles of -pentlandite are however so small, that they are -seldom noticeable, but at Sudbury, Canada, this -is the chief ore of nickel.</p> -<h3><a id="species_Millerite">Millerite</a> -<br />NiS -<br /><i>capillary pyrites</i></h3> -<p>Occurs in needle-like or fibrous -crystals; hardness 3.5; specific gravity -5.5; color brass-yellow; streak -greenish black; luster metallic; -opaque on thin edges.</p> -<p>The fibrous crystals of millerite belong to the -orthorhombic system. The color and streak -suggest pyrite, but the crystals are long and -<span class="pb" id="Page_84">84</span> -slender, while pyrite is in cubes, octahedrons, -etc. If there is any doubt of the identity of this -form, place a piece in nitric acid, and if it is -millerite, it will color the acid green.</p> -<p>It may occur in veins associated with cobalt -and silver minerals, or as a secondary mineral as -at Gap Mine, Penn., or in cavities in sedimentary -rocks. In the last case it usually is in -needle-like crystals growing through calcite -crystals, as at St. Louis, Mo., Keokuk, Iowa, -and Antwerp, N. Y.</p> -<h3 class="center"><span class="sc">The Cobalt Group</span></h3> -<p>As a metal, cobalt is hard, brittle, and of a -grayish color, tinged with red. It was not recognized -as a separate element until 1735, and -even today is one of the minor metals. Cobalt, -chromium and a little tungsten make the alloy -stellite, which has come into large use in making -high-speed tools. The oxide of cobalt (CoO) is -“smalt,” used to give the blue color to porcelain, -pottery, glass, tiles, etc. Invisible ink is made by -diluting cobalt chloride in a large quantity of -water. This solution is a faint pink color and -practically invisible on paper, but if heated it -loses water and turns blue in color, and is perfectly -visible.</p> -<p>Cobalt is another of the metals, of which the -United States does not have an adequate supply. -Sweden, Norway and India were the chief -sources of supply until cobalt was found near the -town of Cobalt in Ontario, Canada, and now -this district furnishes 90% of the world’s supply.</p> -<div class="pb" id="Page_85">85</div> -<h3><a id="species_Cobaltite">Cobaltite</a> -<br />CoAsS -<br /><a href="#Plate_26">Pl. 26</a> -<br /><i>cobalt glance</i></h3> -<p>Usually crystalline in cubes, pyritohedrons -or octahedrons; hardness -5.5; specific gravity 6.1; color reddish -silver-white; streak grayish-black; -luster metallic; opaque on thin edges.</p> -<p>In color cobaltite may appear very like arsenopyrite, -especially if the reddish tinge is not -strong, in which case the mineral can be definitely -determined by putting a piece in nitric -acid. If it is cobaltite the solution will be -colored rose-red, if arsenopyrite there will be no -change of color. The forms of the crystals are -the same as those of pyrite, but the color will -easily distinguish cobaltite from pyrite. This -pink color is characteristically present either in -or about cobalt minerals, being sometimes called -“cobalt bloom.” It is a cobalt-arsenic-oxide -with water of crystallization (Co₃As₂O₈·8H₂O), -which results from the exposure of cobalt and -arsenic minerals to air and moisture. It is the -pink color on the figures of both cobaltite and -smaltite. In Sweden, Norway and India, this is -the chief ore for cobalt, but in the United States -it is rather rare, but is found in Oregon, and at -Cobalt, Canada.</p> -<h3><a id="species_Smaltite">Smaltite</a> -<br />(CoNi)As₂ -<br /><a href="#Plate_26">Pl. 26</a> -<br /><i>gray cobalt ore</i></h3> -<p>Usually occurs in masses; hardness -5.5; specific gravity 6.2; color -tin-white to steel-gray; streak grayish-black; -luster metallic; opaque -on thin edges.</p> -<p>While very like cobaltite, smaltite is almost -never found in crystals, but when crystals are -found, they are cubes. The color is tin-white -<span class="pb" id="Page_86">86</span> -but there is usually a pink tinge visible due to the -presence of small amounts of “cobalt bloom.” -If in any doubt about the determination of this -mineral, put a piece in nitric acid. If it colors -the acid rose-pink, and is non-crystalline it is -pretty surely smaltite; if the acid is not affected -it is arsenopyrite.</p> -<p>Smaltite is found in Kentucky, Missouri, -Colorado, Idaho, California, and at Cobalt in -Canada.</p> -<h3 class="center"><span class="sc">Chromium</span></h3> -<p>This metal gets its name in recognition of the -many colors (<i>chroma</i> “color”), in which its -compounds appear. Chromic oxide is a vivid -green, used to color porcelains, pottery, tiles, -etc., and also as a substitute for the arsenical -greens formerly used in wall-paper. The chromate -of lead is the pigment, well known to artists -as “chrome yellow,” and the bichromate of -potassium is bright red. The metal is obtained -in at least two different forms; one hard, brittle -and so resistant to heat as to be infusible at -temperatures which would volatilize platinum; -the other as a powder which burns brightly if -heated in air. While used in paints, dyes, etc., -its greatest importance is for the making of -ferro-chrome steel, which is used where resistance -to sudden shock is required, as in armor -plate, automobile springs, ball bearings, etc. -With tungsten and cobalt it makes the alloy, -stellite, as noted above.</p> -<p>Chromium was used in relatively small quantities -<span class="pb" id="Page_87">87</span> -before the first world war, and we imported -our supplies from Turkey, India, New Caledonia, -and Rhodesia. During the last war we started a -large-scale development of low-grade ores in -Montana, and can now supply all of our needs -from this source.</p> -<h3><a id="species_Chromite">Chromite</a> -<br />FeCr₂O₄ -<br /><i>chromic iron</i></h3> -<p>Occurs in grains, masses, or isometric -octahedrons; hardness 5.5; -specific gravity 4.4; color black; -streak dark-brown; luster submetallic; opaque -on thin edges.</p> -<p>In form, color and streak chromite resembles -magnetite and franklinite. From the magnetite -it is distinguished by being non-magnetic; from -the franklinite, by being insoluble in hydrochloric -acid, while the franklinite is soluble. -Chromite furnishes practically all the chromium -used in the arts and manufactures. It is a -mineral associated with high temperatures, and -therefore found in dark lavas, serpentine, and -olivine. It occurs in Pennsylvania, Maryland, -New Jersey, Montana, Oregon, Wyoming, and -California.</p> -<h3 class="center"><span class="sc">Tungsten</span></h3> -<p>This element is obtained either as a heavy -dark-gray metal, which is very hard and difficult -<span class="pb" id="Page_88">88</span> -to fuse, or as a dark-gray powder. It is used as -an alloy with iron, one part of tungsten to nine -of steel, to make the ferrotungsten, which has -extraordinary hardness, and is used mostly for -high-speed tools. Tungsten is also one of the -three metals (cobalt, chromium and tungsten) -which are alloyed together to make stellite. -Some of the tungsten supply is also used to -make the films in incandescent lamps, and in -some of the chemical industries. It has but one -important ore, wolframite, and this is found in -the United States in but small quantities; so -that we ordinarily have to import the greater -part of what we use. During the last war, under -the stimulus of high prices and the urge of necessity, -we did find and produce substantial quantities -of tungsten. China is the world’s largest -producer of tungsten ore with Burma second, and -the United States a poor third.</p> -<h3><a id="species_Wolframite">Wolframite</a> -<br />(FeMn)WO₄</h3> -<p>Occurs in monoclinic crystals or -in crystalline masses; hardness 5.5; -specific gravity 7.4; color dark-brown -to black; streak nearly black; luster -submetallic; opaque on thin edges.</p> -<p>If in crystals the form will serve to distinguish -this mineral from cassiterite and ilmenite, the -two which it most resembles; but if it is massive -the only sure way to decide is to put a piece in -strong sulphuric acid; if it dissolves and throws -down a yellow precipitate (tungstic acid) it is -wolframite.</p> -<div class="pb" id="Page_89">89</div> -<p>Like the two other minerals mentioned above -it occurs in veins in igneous rocks, being associated -with high temperatures. As it is almost -insoluble in water, like cassiterite and ilmenite, -it is likely to occur with them in the sands which -are the result of the disintegration of the rocks -which carried the minerals; and so a large part -of the supply today comes from placer deposits.</p> -<p>It is found in Connecticut, North Carolina, -Missouri, Colorado, and California.</p> -<h3 class="center"><span class="sc">Radium, Uranium and Vanadium</span></h3> -<p>These three metals are all rare and occur -together. Radium, discovered in 1898, is a -heavy metal which has proved very useful -because of its radio-activity, that is, its power of -giving off or radiating tiny particles of matter -known as <i>X-rays</i>, part of which are charged with -positive electricity, and part of them with -negative electricity. The ability of these rays -to pass through other substances has made -possible photographing the denser substances -within those less dense, as the bones within the -flesh, or metal within leather or wood, etc. -The rays have proved of great value medicinally, -and are also used to make objects luminous in -the dark. These X-rays are also used in the -study of the ultimate structure of matter, as it -can be thus obtained in such small units.</p> -<p>Uranium is another element which is radio-active -and can be used for many of the same -purposes as radium.</p> -<p>Vanadium, the third of these associated metals, -<span class="pb" id="Page_90">90</span> -and the commonest of the group, is not radio-active. -It is a silvery-white metal, mostly used -as an alloy with steel to give it great hardness.</p> -<h3><a id="species_Carnotite">Carnotite</a> -<br />K₂O·2U₂O₃·V₂O₅·3H₂O -<br /><a href="#Plate_27">Pl. 27</a></h3> -<p>Occurs in earthy masses; color yellow.</p> -<p>This mineral is included here, not -because it is common, but because -it is of such great interest. It is the chief source -of supply in the United States of radium, uranium -and vanadium. It is a lemon-yellow earth -or powder, which looks a little like orpiment. -It is however found in a sandstone, instead of -where hot waters have deposed minerals. From -a ton of this ore about 10 pounds of uranium -oxide, 55 pounds of vanadium and ¹/₁₀₀₀th of a -gram of radium are obtained. Carnotite is found -in south-west Colorado and south-east Utah, and -on Carrizo Mountain on the line between Arizona -and New Mexico.</p> -<h3 class="center"><span class="sc">Mercury</span></h3> -<p>Mercury, or quicksilver, is the only metal -which is liquid at ordinary temperatures. It is -silvery-white in color, with a striking metallic -luster, and at the low temperature of 662° F., -boils and changes to a colorless vapor. Mercury -alloys with certain metals, these alloys being -<span class="pb" id="Page_91">91</span> -known as amalgams. In this way it is especially -useful for the recovery of gold and silver, the -mercury being added to crushed ore, the gold or -silver uniting with the mercury in a liquid amalgam, -which is then drawn off and heated to a -temperature above 662° F., at which temperature -the mercury volatilizes and is recovered, while -the gold or silver remains behind. Mercury -also forms a solid amalgam with tin which is -used to coat glass, the high metallic luster -making the most effective looking glass. It is -also used in medicines (calomel, corrosive sublimate, -etc.), for scientific instruments (thermometers, -barometers, etc.), in cosmetics, in -paints for ship bottoms, etc.</p> -<p>Though there are some 25 minerals of mercury, -only one is common or important as a -source of the metal, cinnabar. The United -States is self-sufficient as far as mercury is concerned, -producing just about as much as it -uses. The leading producers are Spain, Austria, -Italy, and the United States. Commercially -mercury is quoted as quicksilver, and in flasks -of 75 pounds each.</p> -<h3><a id="species_Cinnabar">Cinnabar</a> -<br />HgS -<br /><a href="#Plate_27">Pl. 27</a></h3> -<p>Occurs in massive or earthy form, -or in minute crystals in cavities; -hardness 2.5; specific gravity 8; -color scarlet to dark red; streak vermilion; -luster adamantine; translucent on thin edges.</p> -<p>The bright-red color and the streak are usually -enough to identify this mineral at once, but some -of the darker varieties resemble hematite or -zincite in appearance, but both these have much -<span class="pb" id="Page_92">92</span> -greater hardness. When in crystals they are -tiny hexagonal prisms with pyramids on the end. -Cinnabar is usually found in or near metamorphic -or igneous rocks, either in veins leading -from the igneous rocks, or in metamorphic rocks, -or it may occur disseminated through metamorphic -rocks. It is associated with quartz or -calcite, and may occur with other sulphides -like pyrite, galena, argentite, etc. It is most -abundant in California, but is also found in -Oregon, Washington, Idaho, Arizona, Nevada, -Utah, Texas, and Montana.</p> -<h3 class="center"><span class="sc">Tin</span></h3> -<p>Tin has been known since early Roman times, -and the mines at Cornwall, England, were worked -from that time all through down to the present, -but now they are becoming of minor importance -as they approach exhaustion. The metal is -silvery-white, does not easily tarnish, is -malleable, but has little ductility and little -tensile strength. Tin is mostly used in making -tin plate, a thin sheet of steel covered with tin, -the tin being only 1 to 2% of the total weight. -This tin plate is mostly made into tin cans, and -used as containers for food. Some tin is used in -making solder, tin-foil, tubes for paste, vaseline, -etc., and around 1000 tons per year for weighting -silk. This “weighting” makes the silk heavier -by about 25% and gives it a “rustle,” which, -while much in evidence, is really indicative that -the silk is not pure. The United States produces -very little tin, most of the world’s supply coming -<span class="pb" id="Page_93">93</span> -from the Malay Peninsula, Dutch East Indies, -China, and Bolivia, with small amounts from -several other countries.</p> -<h3><a id="species_Cassiterite">Cassiterite</a> -<br />SnO₂ -<br /><a href="#Plate_28">Pl. 28</a> -<br /><i>tin stone</i></h3> -<p>Occurs in tetragonal crystals, -massive, or in grains and pebbles; -hardness 6.5; specific gravity 7; -color black or dark-brown; streak gray; luster -adamantine; translucent on thin edges.</p> -<p>The crystals are short prisms with pyramidal -ends. Twinning is common. Cassiterite also -occurs in fibrous masses, and when it is weathered -from its original location, is so insoluble and -hard, that it remains as grains and pebbles, -making placer-deposits, from which today three -quarters of the supply is obtained. If pure, the -crystals would be colorless, but impurities of -iron and titanium give it the dark-brown to -black color. Cassiterite may appear very like -rutile, the crystalline forms being identical, but -the reddish tinge of color in the rutile will -separate the two.</p> -<p>Cassiterite is one of those minerals which result -from deposition at very high temperatures, -probably from vapors, and is found in the veins -in igneous rocks, such as light-colored granites, -gneisses, syenites, etc. While not mined in this -country it is found in small quantities in Maine, -Massachusetts, New Hampshire, Virginia, Alabama, -Wyoming, Montana, and California.</p> -<h3 class="center"><span class="sc">Titanium</span></h3> -<p>Titanium, as a metal, is a heavy, gray, iron-like -powder, which is chiefly useful as an alloy -<span class="pb" id="Page_94">94</span> -with iron, giving it toughness, and preventing -bubbles and cracks in casting. It is not as rare as -some other metals which have found a wider use.</p> -<h3><a id="species_Rutile">Rutile</a> -<br />TiO₂ -<br /><a href="#Plate_28">Pl. 28</a></h3> -<p>Occurs in tetragonal crystals, -and in grains; hardness 6.5; specific -gravity 4.2; color red to reddish-brown; -streak yellowish-brown; luster metallic -to adamantine; translucent on thin edges.</p> -<p>Rutile usually occurs in crystals, which are -either short and stout, or in needle-like crystals. -Twinning is common. In form and general -appearance it resembles cassiterite, but the -reddish color, and the yellowish-brown streak -will distinguish the rutile. It is found in similar -rocks, granites, gneisses, syenites, and mica-schists, -the two minerals cassiterite and rutile -often occurring together. This is also true of the -grains, which have been weathered out and are -found in sands and gravels of placer deposits. -It is found in small quantities in all the New -England States, New York, and all down the -Appalachian Mountains, especially at Graves -Mountain, Ga., and in Arkansas and Alaska.</p> -<h3><a id="species_Ilmenite">Ilmenite</a> -<br />FeTiO₃</h3> -<p>Occurs in granular masses, as -black sand, or as tabular hexagonal -crystals; hardness 5-6; specific gravity -4.7; color black; streak brownish-red to -black; luster metallic; opaque on thin edges.</p> -<p>When ilmenite occurs in crystals they are -tabular and resemble hematite in its darker -varieties, but the streak readily distinguishes the -two. In masses it looks like magnetite, but the -lack of magnetism serves to distinguish these -<span class="pb" id="Page_95">95</span> -two minerals. It is very likely to be associated -with cassiterite, rutile, or magnetite in grains -which have weathered out of the original rock, -and have resisted solution and wear. Sands with -a large amount of the above mentioned minerals -are termed “black sands,” some of which are -important for one or another of these minerals.</p> -<p>Ilmenite is a mineral formed at high temperatures, -and probably often deposited from hot -vapors. It is found in granites, syenites, and -gneisses. Among the better known localities -are Orange, N. Y., Litchfield, Conn., Florida, -California, etc.</p> -<h3 class="center"><span class="sc">Platinum</span></h3> -<p>This metal is steel-gray in color, very malleable -and ductile, almost infusible and resists the -action of acids. It is one of the “noble” metals, -much rarer than gold, and so has become popular -for jewelry. It is also used in the manufacture -of sulphuric-acid, in nitrogen-fixation plants, for -chemical utensils, in the electrical industries, and -in dentistry. Platinum in its occurrence is -associated with the certain other equally rare -elements, like iridium, palladium and osmium. -Its use has increased rapidly of late, but the -supply has not kept up with the demand, so -that, whereas in 1906 platinum and gold were -about equally valuable, now the platinum brings -about five times as much as the gold.</p> -<h3><a id="species_Platinum">Platinum</a> -<br />Pt</h3> -<p>Occurs in grains or nuggets; -hardness 4.5; specific gravity 19 -(21 if pure); color steel-gray; luster -metallic; opaque.</p> -<div class="pb" id="Page_96">96</div> -<p>This rare metal is mostly found in placer-deposits, -often with gold. It comes originally -from dark igneous rocks, like peridotite, pyroxenite, -etc., and platinum is found to be associated -with the nickel ores of Sudbury, Canada. While -formerly 90% of the world’s supply of platinum -came from placer mines in the Ural Mountains, -today more than half is produced in Canada and -about a fifth in Russia. In the United States it -is found in California, Oregon, Nevada, and -Alaska.</p> -<h3 class="center"><span class="sc">The Magnesium Group</span></h3> -<p>Magnesium is a silvery-white metal, easily -tarnished by exposure to moist air. Because of -its light weight, less than twice the weight of -water, and strength, it is being substituted for -aluminum, especially in airplanes, where the -question of weight is crucial. It is also used in -automobile and ship production and other machine -industries, and in the manufacture of flares -and incendiary bombs. Magnesium is obtained -chiefly from magnesite, dolomite, and in the -United States as a result of a recently developed -process, from sea water. Magnesium has a -<span class="pb" id="Page_97">97</span> -considerable number of minerals, of which three -are taken up here and several more under the -head of silicates, where both magnesium and -silicon are combined in a mineral.</p> -<h3><a id="species_Spinel">Spinel</a> -<br />MgAlO₄ -<br /><a href="#Plate_29">Pl. 29</a></h3> -<p>Occurs mostly as isometric octahedrons; -hardness 8; specific gravity -3.5; color, red, yellow, green, or -black; streak white; luster vitreous; transparent -on thin edges.</p> -<p>This is a rather rare mineral, but, when in -clear crystals is considered one of the gems. It -was early confused with corundum, and the red -variety called ruby, as it was found in the same -gem-bearing sands in Ceylon, Burma, and Siam. -However the form of the isometric octahedron -as compared with the hexagonal prism of the -corundum, together with the lesser hardness -are sufficient to distinguish the two easily. -The crystals are usually octahedrons, but may -have the corners cut or the edges beveled. -Twins are not uncommon.</p> -<p>The standard color is a clear deep-red, and -such a spinel is known in the gem trade as a -<i>spinel-ruby</i>. If the color is rose-red, it is a -<i>Balas ruby</i>; if orange, it is <i>rubicelle</i>, if of a violet -tinge, <i>almandine</i>. When small quantities of -other elements replace the magnesium, the color -is greatly changed. For example a little iron -present gives the crystals a dark-green to black -color, and the spinel is known as <i>ceylonite</i>. If -there is both iron and chromium present, the -color becomes yellowish or greenish-brown, and -this variety is <i>picotite</i>. When the impurities -<span class="pb" id="Page_98">98</span> -are iron and copper, the color becomes grass-green, -and it is called <i>chlorospinel</i>. A form, in -which the magnesium is completely replaced by -iron, is black in color and termed <i>hercynite</i>, and -occurs fairly abundantly in Westchester Co., -N. Y. From Amity, N. Y., to Andover, N. J., -there is a belt of granular limestone in which -spinel of all colors is found. St. Lawrence Co., -N. Y., is also a rich locality. Bolton, Mass., -Newton, Sterling, and Sparta, N. J., North -Carolina, Alabama, and California all yield -spinel.</p> -<h3><a id="species_Magnesite">Magnesite</a> -<br />MgCO₃</h3> -<p>Occurs in cleavable or compact -porcelain-like masses; hardness 4; -specific gravity 3.1; color white to -gray; luster vitreous; translucent on thin -edges.</p> -<p>Magnesite is white and brittle, and cleaves -perfectly parallel to the faces of the rhombohedron, -but it seldom occurs in crystals. It will -effervesce in warm hydrochloric acid and has -some resemblance to calcite, but can be distinguished -by the greater hardness. It is still -more like dolomite, both having the same color -and cleavage, both effervescing in warm hydrochloric -acid; but the magnesite has half a point -greater hardness and the porcelainous appearance. -Magnesite is used in toilet preparations, -paper making, and mixed with asbestos, as a -covering for heating pipes.</p> -<p>Magnesite is found in Massachusetts, Pennsylvania, -Texas, and in large deposits in California -and Washington.</p> -<div class="pb" id="Page_99">99</div> -<h3><a id="species_Dolomite">Dolomite</a> -<br />(MgCa)CO₃ -<br />Pl. <a href="#Plate_19">19</a> & <a href="#Plate_29">29</a></h3> -<p>Occurs in crystals, or in cleavable -or granular masses; hardness 3.5; -specific gravity 2.8; color white to -pink or gray; streak white; luster vitreous; -transparent on thin edges.</p> -<p>Dolomite crystallizes in the hexagonal system, -in rhombohedrons (hemihedral form), which are -more or less modified by faces on the corners or -edges. The cleavage is parallel to the rhombohedron, -and it will effervesce in warm hydrochloric -acid. Sometimes the crystal faces are -curved, and when this is the case, dolomite is -easily determined. Usually however dolomite -resembles both calcite and magnesite. From the -calcite it is distinguished by the greater hardness, -and from magnesite by lesser hardness and not -being porcelainous in appearance. Some of the -commoner forms are shown on <a href="#Plate_29">Plate 29</a>, crystals -like C being found embedded in anhydrite and -gypsum.</p> -<p>Magnesium is a common element and is likely -to be present wherever lime is being deposited, -so dolomite crystals are common, and much of -the limestone is dolomitic.</p> -<p>It may be found in almost any limestone -section of the country. Some of the finest -crystals of dolomite however come from Roxbury, -Vt., Smithfield, R. I., Hoboken, N. J., -Lockport, Rochester, and Niagara Falls, N. Y., -etc.</p> -<h3 class="center"><span class="sc">Silicon, Silica and the Silicates</span></h3> -<p>Silicon is one of the non-metallic elements, and -does not occur as such in Nature. When isolated -<span class="pb" id="Page_100">100</span> -it is either a dark-brown powder, or steel-gray -crystals. However silicon is next to oxygen in -its importance in making the crust of the earth. -Forty-seven per cent of the surface rocks are -composed of oxygen, and 28% of silicon, the -latter appearing in a host of minerals. The -oxide of silicon is termed silica (SiO₂), its crystal -form being quartz, the commonest of all minerals. -In non-crystalline form silica is also widely distributed, -as chalcedony and opal, even appearing -in the tissues of animals and plants, as in the -feathers of birds, the shells of certain Protozoa -(Radiolaria), the spicules of sponges; and in -plants, as the shells of diatoms, and in the stalks -of grasses, especially cereals and bamboo. Silica -in the form of sand is widely used in making -glass, porcelain, china, etc., and in the various -cements.</p> -<p>Then there are a considerable number of acids -of silicon, which do not occur in Nature, but their -salts do, and make a host of minerals, which are -known as the silicates, such as mica, feldspar, -hornblende, etc. Either as quartz, or as -silicates, silicon is represented in most all the -igneous and metamorphic rocks and in many of -the sedimentary rocks.</p> -<h3><a id="species_Quartz">Quartz</a> -<br />SiO₂ -<br /><a href="#Plate_30">Pl. 30</a></h3> -<p>Occurs as hexagonal crystals, or -in grains or masses; hardness 7; -specific gravity 2.65; colorless when -pure; luster vitreous; transparent on thin edges.</p> -<p>Quartz is not hard to identify. Its hardness -and the crystal-form separate it from most all -other minerals. It is the most common mineral, -<span class="pb" id="Page_101">101</span> -making 12% of the earth’s crust. The usual -crystal form is a hexagonal prism with the sides -horizontally striated, and a six-sided pyramid on -one or both ends. This six-sided pyramid is -really two rhombohedrons, a right-handed one -and a left-handed one, so that the alternate -faces of the pyramid may show peculiarities, for -instance three may be large and three small, as -in Fig. B, <a href="#Plate_30">Plate 30</a>, or the alternate ones may be -duller or etched in some manner. The crystals -are clear and when pure colorless, but there is a -tendency for some slight impurity to color them -almost any hue.</p> -<p>The most perfect double-ended crystals form -only where growth is possible in all directions, -as in clay. In cavities and caves there is an -opportunity for the crystals to grow in toward -the open spaces, and in such places, one finds -fine large crystals; the Alps, Brazil, Japan, and -Madagascar being especially famous localities. -The largest quartz crystal on record is one 25 -feet in circumference which came from Madagascar. -In this country the caves at Little Rock, -Ark., have furnished some very fine large crystals. -Smaller, but very clear crystals, come from about -Herkimer, N. Y. Some of these have been used -as “Rhine-stones” and as cheap imitations of -diamonds. Clear quartz is beautiful enough to -be a gem, but it is too common to interest people -as jewelry, however many objects of art have -been carved from it. One of these took the form -of crystal balls, which, through the Middle -Ages particularly, developed into a form of -mysticism. The gazing into the crystal ball was -<span class="pb" id="Page_102">102</span> -supposed to give some people supernatural -vision. It seems to be a form of hypnotism, -gazing at the bright reflecting surface tiring the -eye, and making possible visions, which are -subjective rather than anything external.</p> -<p>Silica is slightly soluble in water, especially -when it is alkaline; so that most river-, lake-, and -sea-waters have some silica in solution, and are -carrying it from one place to another. The -waters, which percolate through the rocks, carry -even more, and when they come out into open -spaces, they give up some of the silica, making -crystals lining these openings, whether fissures or -cavities. Not infrequently these silica-bearing -waters dissolve out some other crystal, and then -deposit in its place silica, thus making a crystal -which has the form of what was dissolved, rather -than that of quartz. Such a form is known as a -pseudomorph.</p> -<p>When molten masses of igneous rock were -cooling the quartz crystals had their faces interfered -with as they grew, and we have resulting -crystalline quartz, simply filling in the spaces -between the other crystals, such as feldspar and -mica, in the granite. Quartz is a large component -in many igneous rocks, also in metamorphic -rocks, and certain sedimentary rocks -like sandstone are almost wholly made up of -quartz grains. Quartz is also the gangue mineral -in many veins. In this case it seems to have been -deposited from hot water or vapors, as they rose -from cooling magmas. With it are associated -all sorts of metallic ores as has been suggested.</p> -<p>Quartz has been largely used to make imitations -<span class="pb" id="Page_103">103</span> -of other much rarer minerals, sometimes -in its crystalline form to imitate the diamond, -at other times ground and made into a “paste,” -which is colored to imitate other gems. This -paste is a mixture of about 4 parts of quartz, -5 parts of red lead and 1 part of potassium carbonate, -melted and cooled slowly. It is clear and -has a brilliant luster like the diamond. If some -coloring matter is put into it it can be used for -rubies, sapphires, etc. When there is any reason -to think that this is being used, it is easily -detected by being so much softer than any of the -true gems, and even than true quartz. Quartz -will scratch glass readily, but this imitation has -only the hardness of very soft glass, or about 5.</p> -<h3 class="center"><span class="sc">Varieties of Quartz</span></h3> -<p><b>Rock crystal</b> is the term applied to quartz when -it is clear and colorless.</p> -<p><b>Milky quartz</b> is the milky variety, the whiteness -being due to imperfections in the crystallization, -such as cracks, bubbles, etc.</p> -<p><b><a id="species_SmokyQuartz">Smoky quartz</a></b> is the cloudy brown-colored -variety, which results from the presence of small -quantities of organic matter (hydrocarbons) in -the quartz. If the color is so dark as to be almost -black it is termed <b>morion</b>. In the above cases -the color will disappear if the stone is heated. -Pebbles of smoky quartz from Cairngorm, Scotland, -have been so widely used as semiprecious -stones that they have come to be known as -<b>cairngorms</b>.</p> -<p><b>Citrine</b>, or <b>false topaz</b>, is a clear yellow variety, -the color again due to the presence of organic -<span class="pb" id="Page_104">104</span> -matter. It is distinguished from true topaz by -the lesser hardness, this having the hardness of -7, while true topaz has a hardness of 8.</p> -<p><b><a id="species_Amethyst">Amethyst</a></b> is quartz with a violet color, due to -the presence of small quantities of manganese. -To be suitable for cutting into gems, the color -must be deep or the small pieces will appear almost -colorless. It is widely used today as a -semiprecious stone in jewelry; and in the fifteenth -century it had the traditional virtue of making the -wearer sober-minded, whether he had taken too -freely of wine, or was over excited by love-passion.</p> -<p><b><a id="species_RoseQuartz">Rose quartz</a></b> gets its pale-red color from the -presence of a small amount of titanium. It is -widely distributed, but is more abundant in the -Black Hills of South Dakota.</p> -<p><b>Aventurine</b> is quartz which has inclosed tiny -scales of mica or hematite giving it a spangled -appearance.</p> -<p><b><a id="species_Prase">Prase</a></b> is a green quartz, the color being due to the -inclusion of fibrous crystals of green actinolite.</p> -<p><b>Cat’s Eye</b> is a quartz which has inclosed silky -fibers of asbestos. When this is cut parallel to -the fibers, the effect is opalescent. The colors -are greenish, yellowish-gray, and brown. This -form, however, is not to be confused with the -true or Oriental Cat’s Eye, which is chrysoberyl -and has the hardness of 8.</p> -<h3><a id="species_Chalcedony">Chalcedony</a> -<br />SiO₂</h3> -<p>Non-crystalline, occurring in botryoidal, -stalactitic or concretionary -masses; hardness, 7; specific gravity, -2.65; color white when pure; luster waxy; translucent -to transparent on thin edges.</p> -<div class="pb" id="Page_105">105</div> -<p>In addition to the crystalline form, silica is -freely deposited in an amorphous or cryptocrystalline -form which has the same properties as -quartz, except the crystal faces. This is called -chalcedony, and it occurs in seams, cavities and -free surfaces. When the surface of a chalcedony -deposit is free it has a waxy luster. It is generally -very brittle and breaks in a peculiar splintery -manner. Like quartz it also has a great -many varieties, according to the impurities present. -Its wide distribution, hardness, and the -manner in which it can be chipped have made -this a most important stone in the history of the -development of civilization. The early men first -broke it into rough tools, such as knives, axes, -spear points, etc., and used these as cutting tools, -of one sort or another, because they held their -edge better than most stones. We apply, to the -people who used only these chipped stones as -tools, the term “<i>Men of the Old Stone Age</i>,” or the -period is termed the <i>Palæolithic Age</i>. Later men -learned how to grind the edge to a smoother -outline, and this much shorter period is termed -the <i>Neolithic Age</i>. The use of flints for the first -tools is world-wide, and the American Indian -when discovered was still using chalcedony in its -rough-hewn state.</p> -<div class="verse"> -<p class="t2">“There the ancient Arrow-maker</p> -<p class="t0">Made his arrow heads of sandstone,</p> -<p class="t0">Arrow heads of chalcedony,</p> -<p class="t0">Arrow heads of flint and jasper,</p> -<p class="t0">Smoothed and sharpened at the edges,</p> -<p class="t0">Hard and polished, keen and costly.”</p> -</div> -<div class="pb" id="Page_106">106</div> -<p><b>Chalcedony</b> is the proper term to use when the -color is white to translucent, in which case the -surfaces are usually botryoidal and waxy.</p> -<p><b><a id="species_Carnelian">Carnelian</a></b> is chalcedony which is clear red in -color and translucent. This is one of the first -stones used for ornamental purposes and for engraving. -Carnelians with figures engraved on -them were used by the Egyptians, Assyrians -and The Children of Israel, at least 2000 <span class="small">B.C.</span>; -and the Egyptian scarabs of the fifth or sixth -century <span class="small">B.C.</span>, were often carved from this variety -of chalcedony, as well as from jasper and agates.</p> -<p>The brownish varieties are termed <i>sard</i>.</p> -<p><b><a id="species_Chrysoprase">Chrysoprase</a></b> is an apple-green variety of -chalcedony the color being due to the presence -of nickel oxide. This is by no means as common -as most of the varieties of chalcedony, and was -long prized as a gem.</p> -<p><b><a id="species_Plasma">Plasma</a></b> is chalcedony with a leek- to emerald-green -color, and the same stone when it has small -red spots of jasper in it is termed <i>blood-stone</i>, -or <i>heliotrope</i>. These red spots are said by tradition -to be drops of the blood of Christ.</p> -<p><b><a id="species_Jasper">Jasper</a></b> is a deep red chalcedony, the color being -due to hematite, which is so abundant as to make -it opaque. A brown variety colored by limonite -is also called jasper, and even green jaspers are -found. In all cases the opaque character is -common.</p> -<p><b><a id="species_Flint">Flint</a></b> is an impure brown chalcedony, usually -forming concretions. The color is due to organic -matter. Flint is mostly found in limestone or -chalk, and the concretions are the result of the -small particles of silica scattered through the -<span class="pb" id="Page_107">107</span> -rock being dissolved, and then reprecipitated -about some organic center. Generally the silica -was obtained by the dissolution of small fossils, -like the shells of diatoms or sponge spicules.</p> -<p><b><a id="species_Hornstone">Hornstone</a></b> and <b><a id="species_Chert">Chert</a></b> are simply impure varieties -of flint, brown in color, and with a splintery -fracture.</p> -<p><b><a id="species_Agate">Agate</a></b>, <a href="#Plate_32">Plate 32</a>, is a banded or cloudy chalcedony -which has formed in a cavity, the layers of -different color representing deposition from -water, carrying first silica with one impurity, -then later, silica with another impurity. Gradually -the cavity has been thus filled with silica; -and when the mass is freed by the weathering -away of the surrounding rock, these banded -masses are found. Sometimes the manner of -deposition has changed, and while the outer part -of the cavity was filled with chalcedony, the -central part will contain quartz crystals. On -account of the beauty of the colors, and the unusual -way in which they may be developed, -agates are widely used for semiprecious jewelry -and objects of art, and this has been true since -ancient times, the name itself coming from the -River Achates in Sicily. The center for cutting -and polishing agates is at Oberstein, Germany, -where this work has been carried on since the -middle of the fifteenth century. In spite of the -many fine natural colors in agates, they are sometimes -artificially colored, in many cases by methods -which are kept as “trade secrets.” The -color seldom penetrates far; so that even slight -chipping reveals whether an inferior agate has -been taken and colored up, or whether the stone -<span class="pb" id="Page_108">108</span> -is natural. Moss agates are chalcedony which -has inclosed dendritic masses of some one of the -manganese compounds as shown under manganite, -<a href="#Page_73">p. 73</a>.</p> -<p><b><a id="species_Onyx">Onyx</a></b> is a variety of agate where the bands are -alternately black and white; while <b>sardonyx</b> is -agate with red or brown bands alternating with -the white. Such agates as these are especially -desirable for cameo work, where the figure is -carved in the chalcedony of one color, and the -other color makes the background.</p> -<p><b>Silicified</b> or <i>agatized wood</i> is a form of chalcedony, -where silica has replaced wood, molecule -by molecule; so that in good specimens, all the -structure of the wood is still retained, and when -thin sections are made it can be studied under -the microscope almost as well as modern wood. -This takes place under water, usually, if not always, -in fresh water. Such fossilized wood is -widely distributed in the western United States, -the most famous cases being the Fossil Forest of -Arizona, now a National Reservation, and the -fossil trees in the Yellowstone National Park.</p> -<h3><a id="species_Opal">Opal</a> -<br />SiO₂·H₂O -<br /><a href="#Plate_33">Pl. 33</a></h3> -<p>Non-crystalline, massive, stalactitic -or nodular; hardness, 6; specific -gravity 2; all colors; luster vitreous, -resinous, or pearly; transparent on thin -edges.</p> -<p>Opal differs from chalcedony in having water, -usually about 10%, incorporated in its structure. -This is water of crystallization, and not firmly -held; so that, if opal is heated in a closed tube to -above 100 C., it is given off as a vapor. Opal is -<span class="pb" id="Page_109">109</span> -distinguished from chalcedony by its lesser hardness, -and the resinous to pearly luster. It forms -in cavities, in layers often of extreme thinness.</p> -<p>Opal is originally the product of the dissolution -of silicate minerals in hot acid waters, the resulting -gelatinous silica, when it is deposited and -hardened, becoming the opal. There are many -varieties, some of them highly prized as gems in -spite of the moderate hardness and opacity of -the mineral. Gem-quality opal gets its opalescent -character from the successive deposition -of thin films of opal, the light penetrating and -being reflected from different films. This breaks -up the white light and causes the play of colors -which is the charm of this gem.</p> -<p><b>Precious opal</b>, in which the play of colors is -finest, comes mostly from Hungary, Mexico, and -Queensland. The opal was a favorite stone from -before Roman times, and in its early history was -a charm against the “evil eye.” During the -nineteenth century for some reason it came to be -considered an unlucky stone.</p> -<p><b><a id="species_FireOpal">Fire opal</a></b> is a hyacinth-red to honey-yellow -variety, which has a fire-like play of color, and -is found in Mexico and Honduras.</p> -<p><b>Common opal</b> does not have the play of color, -but comes in a variety of colors; is waxy or greasy -in luster; and occurs mostly as fillings of seams or -cavities, especially those in igneous rocks, like -the steam holes in lavas, etc. It is found in -Cornwall, Penn., in Colorado, California, etc.</p> -<p><b>Opal-agate</b> is a variety in which there are -color bands, and it is widely distributed.</p> -<p><b>Opalized wood</b> is formed in exactly the same -<span class="pb" id="Page_110">110</span> -manner as agatized wood, much of the fossil wood -called silicified being really opalized.</p> -<p><b>Siliceous sinter</b> is the porous mass of opal -which is so frequently deposited about hot -springs and geysers. It is readily recognized by -its porous character.</p> -<p>The shells of the diatoms, which are microscopic -plants, are made of opal; and while they -are so small, there is certainly no other plant so -abundant or omnipresent, living as it does in -every pool, lake, or sea by the millions. These -shells are very indestructible so that they -accumulate at the bottom of ponds, bogs, and -sea-bottoms, making at times extensive deposits. -This material in quantities is termed diatomaceous -earth, or <b>tripolite</b> (from Tripoli where it was -first used commercially). It is used as a polishing -powder for metals, marble, glasses, etc.</p> -<h3 class="center"><span id="species_Feldspar" class="sc">The Feldspars</span></h3> -<p>The term feldspar is a family name for a large -variety of very common minerals, which altogether -make up nearly 60% of the crust of the -earth, being the predominant part of granites, -gneisses, and lavas. In composition they are -silicates of aluminum, together with potassium, -sodium and calcium, and their mixtures. They -may be tabulated as follows:</p> -<dl class="undent"><dt>1. KAlSi₃O₈, <i>orthoclase</i>, the silicate of aluminum and potassium.</dt> -<dt>2. NaAlSi₃O₈, <i>albite</i>, the silicate of aluminum and sodium.</dt> -<dt>3. CaAlSi₂O₈, <i>anorthite</i>, the silicate of aluminum and calcium.</dt> -<dt>4. Mixtures of 1 and 2 are <i>alkalic feldspar</i>.</dt> -<dt>5. Mixtures of 2 and 3 are <i>plagioclase feldspar</i>.</dt></dl> -<div class="pb" id="Page_111">111</div> -<p>Orthoclase is monoclinic, but the rest of the -feldspars are triclinic. If crystals are available -they may be short and stout, or tabular and thin, -but as the feldspars are mostly components of the -igneous rocks, where perfect crystals have not -had a chance to grow, they are mostly determined -by their hardness and cleavage. The hardness -of all the feldspars is 6 or very close to it.</p> -<p>They all have three planes of cleavage, two of -which are good and intersect either at 90° as in -orthoclase, or at about 86° as in the plagioclase -series; while the third cleavage plane is imperfect. -In figure 1, <a href="#Plate_34">Plate 34</a>, a and b are the two perfect -cleavages, while c is the imperfect one. Breaking -into such cleavage masses as the one illustrated -is characteristic of feldspar. The specific gravity -ranges from 2.55 to 2.75. The luster is vitreous, -and the color white, ranging to various shades -of gray and pink, and, sometimes in recent lavas, -colorless.</p> -<p>Twinning is very common and helps to distinguish -orthoclase from the plagioclase feldspars. -In orthoclase the twins are simple, that is, only -two crystals growing together, and are united -on one of the faces, as if one of them had been -revolved 180° with the other; or, while related to -each other as in the preceding case, they may -seem to grow through each other. On <a href="#Plate_34">plate 34</a> -are three orthoclase crystals showing this simple -type of twinning. The first (A) is a simple crystal; -the second (B) shows the simplest type of twinning -where the left-hand crystal has revolved -<span class="pb" id="Page_112">112</span> -180° on the p face, and the end is composed, half -of the upper end of one crystal, and half of the -lower end of the adjacent crystal. The presence -of reëntrant angles calls attention to the twinning. -The third figure (C) is a case of intergrowing -crystals.</p> -<p>In the plagioclase feldspars twinning is multiple, -a large number of crystals, each thin, -sometimes as thin as paper, growing side by side, -the first one in normal position, the next at 180° -with it, the third revolved 180° to the second and -thus parallel to the first, and so on. The result -is first of all a striated appearance, and second -that, as plagioclase crystals have their prism -faces intersecting at 86°, there is a series of low -roofs and valleys, which are best seen by holding -the piece of feldspar so the light reflects from a -cleavage face, when it will appear striated; then -by tilting it about 8 degrees a second set of reflections, -also appearing striated, will appear. -The light was first reflected from one side of the -roofs, and in the second case from the other -side. Figure D, <a href="#Plate_34">Pl. 34</a>, is a diagram showing the -relation of the individual crystals in a multiple -twinned piece of plagioclase, in which the crystals -are represented as rather large. <a href="#Plate_35">Plate 35</a>, -under labradorite, shows a photograph of a cleavage -piece, on which is readily seen the striation -which is characteristic of the plagioclase feldspars.</p> -<p>Mixtures of albite and anorthite occur in bewildering -numbers, one or the other predominating, -and each mixture being uniform throughout -the crystal and in the whole mass; so each combination -is a mineral, each with its special properties; -<span class="pb" id="Page_113">113</span> -but the different plagioclase feldspars are -so similar in appearance, that by the naked eye -it is impossible to separate the closely related -ones. This can be done under the microscope by -studying the angles at which light is cut off, and -also by chemical analyses. For our purposes six -types will suffice to illustrate the group, and their -composition may be indicated as follows.</p> -<p>Albite is albite with up to 15% of anorthite -mixed with it.</p> -<p>Oligoclase is albite with from 15-25% of -anorthite mixed with it.</p> -<p>Andesite is albite with from 25-50% of anorthite -mixed with it.</p> -<p>Labradorite is anorthite with from 25-50% -of albite mixed with it.</p> -<p>Bytownite is anorthite with from 15-25% of -albite mixed with it.</p> -<p>Anorthite is anorthite with up to 15% of -albite mixed with it.</p> -<p>The best method for distinguishing these -feldspars of the plagioclase group is to measure -the angle between the two perfect cleavage faces, -and even this requires careful measurement. The -angles between these faces are as follows:</p> -<table class="center" summary=""> -<tr><td class="l">Orthoclase </td><td class="l">90°</td></tr> -<tr><td class="l">Microcline </td><td class="l">89° 30′</td></tr> -<tr><td class="l">Oligoclase </td><td class="l">86° 32′</td></tr> -<tr><td class="l">Andesite </td><td class="l">86° 14′</td></tr> -<tr><td class="l">Labradorite </td><td class="l">86° 14′</td></tr> -<tr><td class="l">Bytownite </td><td class="l">86° 14′</td></tr> -<tr><td class="l">Anorthite </td><td class="l">86° 50′</td></tr> -</table> -<h3><a id="species_Orthoclase">Orthoclase</a> -<br />KAlSi₃O₈</h3> -<p>Occurs in granites, syenites, -gneisses and light-colored lavas; -hardness, 6; specific gravity, 2.57; -color white to gray or pink; cleavage in two directions -<span class="pb" id="Page_114">114</span> -perfect and at 90°, in the third direction -imperfect; luster vitreous; translucent on thin -edges.</p> -<p>Orthoclase is monoclinic, and when formed in -cavities develops as crystals, but it is usually a -constituent of igneous rocks, in which case the -crystals have not had the opportunity to develop -the crystal faces, and the orthoclase is in grains -or irregular masses; and the best way of determining -the mineral is the cleavage, the two -perfect cleavage planes intersecting at right -angles. Twinning is frequent but of the simple -type, only two crystals being united, similar to -either B or C on <a href="#Plate_34">plate 34</a>.</p> -<p>It is found in granites, gneisses or lavas, wherever -they occur, being especially characteristic -of the granites of the Rocky Mountains.</p> -<h3><a id="species_Microcline">Microcline</a> -<br />KAlSi₃O₈ -<br /><a href="#Plate_35">Pl. 35</a></h3> -<p>Occurs in granites and gneisses -as crystals or irregular masses; hardness, -6; specific gravity, 2.56; color -white to gray, pink, or greenish; luster vitreous; -translucent on thin edges.</p> -<p>Microcline has the same composition as orthoclase, -but is in the triclinic system, the c axis -being inclined a half degree away from a right -angle with the b axis. This is best seen in the -cleavage pieces, the two perfect cleavage planes -meeting at 89° 30′, and this is the only test for -determining this mineral by the unaided eye. -Pike’s Peak is the best known locality for microcline, -and there it occurs in fine large crystals -of greenish color, which are known as <i>Amazon -stone</i>.</p> -<div class="pb" id="Page_115">115</div> -<h3><a id="species_Albite">Albite</a> -<br />NaAlSi₃O₈</h3> -<p>Occurs in small crystals, or more -often in lamellar masses in granites -or in seams in metamorphic rocks; -hardness, 6; specific gravity, 2.62; color white to -gray; luster vitreous.</p> -<p>Albite may occur in simple crystals, in which -case the two perfect cleavage planes meet at an -angle of 86° 24′. However, it is much more -frequently found twinned in the multiple manner, -the individual crystals often being as thin as -paper. This gives rise to a fine striation on the -end of a crystal, or on the surface made by the -imperfect cleavage plane. Where the crystals -are extremely thin, the surface may have a pearly -luster. Albite types of granite often inclose -secondary minerals, that are prized as gems, such -as topaz, tourmaline, and beryl.</p> -<p>It is found at Paris, Me., Chesterfield, Mass., -Acworth, N. H., Essex Co., N. Y., Unionville, -Penn., and in Virginia, and throughout the -Rocky Mountains.</p> -<h3><a id="species_Oligoclase">Oligoclase</a> -<br />(NaCa)AlSi₃O₈</h3> -<p>Generally found in cleavable -masses in granites and lavas, rarely -in crystals; hardness, 6; specific -gravity, 2.65; color white, greenish or pink; luster -vitreous; translucent on thin edges.</p> -<p>Oligoclase is a plagioclase feldspar and is distinguished -by its two perfect cleavage planes -meeting at an angle of 86° 32′, but otherwise it is -very like albite. Crystals are not common, and -it occurs mostly in masses, making one of the -components of granite or lava.</p> -<p>It is found in St. Lawrence Co., N. Y., Danbury -<span class="pb" id="Page_116">116</span> -and Haddam, Conn., Chester, Mass., -Unionville, Penn., Bakersville, N. C., etc.</p> -<h3><a id="species_Labradorite">Labradorite</a> -<br />(NaCa)AlSi₃O₈ -<br /><a href="#Plate_35">Pl. 35</a></h3> -<p>Usually found in cleavable masses -in granites and lavas; hardness, 6; -specific gravity, 2.71; color gray or -white, often with a play of colors; -luster vitreous; translucent on thin edges.</p> -<p>Labradorite is distinguished by having the two -perfect cleavage planes meet at 86° 14′. The -iridescent play of color is also very characteristic -and is generally present. It is due to the -inclusion of minute impurities. This feldspar -is usually associated with granites or lavas in -which the dark minerals predominate. It gets -its name from being the feldspar of the granites -of Labrador, and is also found in the granites of -the central part of the Adirondack Mountains -and the Wichita Mountains of Arkansas.</p> -<h3 class="center"><span class="sc">The <a id="species_Pyroxene">Pyroxene</a> Group</span></h3> -<p>The minerals of this group are generally associated -with feldspars, and make the dark-colored -component of granites, gneisses and -lavas. This is especially true of those which -have some iron in the crystal. Pyroxenes are -salts of metasilicic acid (H₂SiO₃), in which the -hydrogen (H) has been replaced by calcium, -magnesium, iron, etc. The commoner minerals -are orthorhombic or monoclinic, and all agree in -their crystal habit, being short stout prisms, with -the vertical edges so beveled that a cross section -is eight-sided. The cleavage is good in two directions, -<span class="pb" id="Page_117">117</span> -parallel to the beveling faces (m in figure -b, <a href="#Plate_36">Plate 36</a>), and they intersect at an angle of -87°. This is very characteristic, and if one has a -crystal broken across, it is easy to see and measure -this angle of intersection. These pyroxenes -have the same chemical composition as the corresponding -series of amphiboles, but the two are -distinguished by several features. Pyroxenes -are short and stout crystals, while amphiboles -are long and either blade- or needle-like; pyroxenes -are eight-sided in cross section, while -amphiboles are six-sided; in pyroxenes the cleavage -planes intersect at 87°, while in amphiboles -they intersect at 55°. The minerals of this group -are most frequently one of the components of a -lava or granite, and are less frequently associated -with metamorphic rocks. Three are common; -enstatite, hypersthene, and augite.</p> -<h3><a id="species_Enstatite">Enstatite</a> -<br />MgSiO₃</h3> -<p>Usually occurs in lamellar or fibrous-lamellar -masses in dark lavas; -hardness, 5.5; specific gravity, 3.3; -color gray, bronze or brown; luster vitreous, -translucent on thin edges.</p> -<p>Enstatite rarely occurs in crystals, but when it -does they are orthorhombic. Usually it is in irregular -masses with the cleavage angles, typical -of pyroxene. The color is light, that is gray or -brownish, and the streak white or nearly so. In -most respects it is similar to hypersthene, which -has the same composition, except that a large -part of the magnesium is replaced by iron, and -there are all sorts of gradations between the two -minerals. When some iron takes the place of -<span class="pb" id="Page_118">118</span> -magnesium, the color darkens to, or towards -bronze, until when about a third of the magnesium -is so replaced, and the color is fully bronze, -this variety is called <i>bronzite</i>. Bronzite is present -in some of the dark lavas like gabbro and -peridotite. Enstatite is found in the Adirondack -Mountains, at Brewster and Edwards, N. Y., etc.</p> -<h3><a id="species_Hypersthene">Hypersthene</a> -<br />(MgFe)SiO₃</h3> -<p>Occurs in cleavable masses in -dark lavas; hardness, 5.5; specific -gravity, 3.4; color dark-brown or -greenish-brown; luster vitreous; translucent on -thin edges.</p> -<p>Hypersthene is a pyroxene in which magnesium -and iron are present in about equal quantities. -It is similar to enstatite, except that the -color is darker, and the streak gray or brownish-gray -in color. These two minerals grade into -each other, so that there are cases where it is -simply a matter of preference as to which name -should be given to the mineral. This form is -associated with dark lavas, of the gabbro or -peridotite type, in such places as the Adirondack -Mountains, Mount Shasta in California, Buffalo -Peaks, Colo., etc.</p> -<h3><a id="species_Augite">Augite</a> -<br />CaMg(SiO₃)₂, MgAlSiO₆ + Fe₂O₃ -<br /><a href="#Plate_36">Pl. 36</a></h3> -<p>Usually occurs in short stout -monoclinic crystals; hardness, 5.5; -specific gravity, 3.3; color dark-green -to black; luster vitreous; -translucent on thin edges.</p> -<p>Augite is a complex pyroxene having some iron -and aluminum always present in it, but the -amount not a fixed quantity. It is by far the -<span class="pb" id="Page_119">119</span> -commonest of the pyroxenes and has a wide distribution, -both in the sorts of lavas in which it -appears, and in the world. It is commonly -the dark component of such lavas, as gabbros and -peridotites, and also is common in metamorphic -rocks, especially impure crystalline limestones. -It is found at Raymond and Mumford, Me., -Thetford, Vt., Canaan, Conn., in Westchester, -Orange, Lewis and St. Lawrence Counties of N. -Y., in Chester Co., Penn., at Ducktown, Tenn., -Templeton, Canada, etc.</p> -<h3 class="center"><span class="sc">The <a id="species_Amphibole">Amphibole</a> Group</span></h3> -<p>The amphiboles are a group of minerals made -up of the same chemical elements as the pyroxenes, -but with the molecular arrangement different, -which appears in the forms of the crystals. -The commoner ones are all monoclinic but contrast -with the pyroxenes as follows. Amphiboles -are long and slender crystals, while pyroxenes -are short and stout; amphiboles are six-sided, -while pyroxenes are eight-sided; amphiboles -have the two perfect cleavages intersecting at -55° and 125°, while those of pyroxene intersect -at 87° and 93°. With the above in mind it is -easy to place the minerals in their proper group, -but inside the group it is not always so easy to -distinguish one from another. This group is -associated rather with metamorphic rocks than -with igneous rocks, with which the pyroxenes are -mostly associated. The three commoner minerals -of the group are tremolite, actinolite, and -hornblende.</p> -<div class="pb" id="Page_120">120</div> -<h3><a id="species_Tremolite">Tremolite</a> -<br />(CaMg)₃(SiO₃)₄ -<br /><a href="#Plate_37">Pl. 37</a></h3> -<p>Occurs in long prismatic crystals -or in columnar or fibrous masses; -hardness 5.5; specific gravity, 3; -color white to gray; luster vitreous; transparent -on thin edges.</p> -<p>The long prismatic crystals of tremolite occur -especially where dolomitic limestones have been -altered by metamorphism. Sometimes these -crystals grow side by side, making fibrous masses, -where the long slender crystals can be picked -apart with the fingers, and yet are flexible, and -tough enough so that they can be felted together. -This is termed asbestos, which, because it is -infusible and a poor conductor of heat, is much -used to make insulators, fire-proof shingles, and -all sorts of fireproof materials. The varieties in -which the crystals are finer and silky in appearance, -like the one illustrated on <a href="#Plate_38">Plate 38</a> are -termed <i>amianthus</i>. There are other minerals, -such as actinolite and serpentine, which occur in -the same manner, and are also called asbestos, the -serpentine variety being just now the most important -commercially.</p> -<p>Tremolite is found at Lee, Mass., Canaan, -Conn., Byram, N. J., in Georgia, etc.</p> -<h3><a id="species_Actinolite">Actinolite</a> -<br />(CaMgFe)₃(SiO₃)₄</h3> -<p>Occurs in radiating crystals, or -in fibrous masses; hardness, 5.5; -specific gravity 3; color pale- to dark-green; -luster vitreous; translucent on thin edges.</p> -<p>Except for its green color, this mineral is very -like tremolite. The difference between the two is -due to the small amount of iron in the actinolite. -It is usually found in schists, and the radiating -<span class="pb" id="Page_121">121</span> -character of the crystal groups is enough to -determine the mineral, if it is already clear that -it is one of the amphiboles. Occasionally it occurs -with the crystals parallel to each other, making -one of the forms of asbestos.</p> -<p>Actinolite is found at Warwick, Edenville, and -Amity in Orange Co., N. Y., at Franklin and -Newton, N. J., Mineral Hill and Unionville, -Penn., Bare Hills, Md., Willis Mt., Va., etc.</p> -<h3><a id="species_Hornblende">Hornblende</a> -<br />(CaMgFe)₃(SiO₃)₄CaMgAl₂(SiO₄)₃ -<br /><a href="#Plate_37">Pl. 37</a></h3> -<p>Occurs in well-defined crystals, in -grains and in masses; hardness, 5.5; -specific gravity 3.2; color black, -dark-green, or dark-brown; luster -vitreous; translucent on thin edges.</p> -<p>In composition hornblende corresponds to -augite, but occurs in long slender, six-sided -crystals with cleavage planes intersecting at 55°, -so that it is a typical amphibole. It occurs in a -very wide range of rocks, such as granite, syenite, -diabase, and gabbro; and in such metamorphic -rocks as schists and gneisses; and sometimes -igneous rocks are made up almost entirely of -hornblende, when they are known as amphibolites -or hornblendite. It is found all through the -New England States, down along the Piedmont -Plateau, through the Blue Ridge Mountains, -and in many of the western mountainous areas.</p> -<h3 class="center"><span class="sc">The <a id="species_Garnet">Garnet</a> Group</span></h3> -<p>The garnets are a series of double silicates, -which occur with surprisingly uniform characters. -They are all isometric, and occur either -<span class="pb" id="Page_122">122</span> -as dodecahedrons, or as the 24-sided figure (the -trapezohedron), which is formed by the beveling -of the edges of the dodecahedron, and developing -these new faces to the exclusion of the dodecahedron -faces. Combinations of the dodecahedron -and trapezohedron (36 faces) may occur. All -the garnets have a hardness of 7 to 7.5, and the -specific gravity runs from 3.2 to 4.3, according to -the composition. In size they run from as small -as a grain of sand up to as large as a boy’s marble, -and occasionally even to four inches in diameter. -The color varies with the composition, from colorless -to yellow, red, violet, or green. There is no -cleavage, and the luster is always vitreous.</p> -<p>Garnets are usually accessory minerals, found -in metamorphic rocks, though they are sometimes -also present in granites and lavas. They are -always segregations which have taken place in -the presence of high temperatures. When clear -and perfect several of the garnets are used as -gems. On the other hand some of the common -garnets occur in such quantities that they are -crushed and used as abrasives, for such work -as dental polishes, or for leather and wood -polishing.</p> -<p>The following is the composition of some of the -commoner garnets.</p> -<table class="center" summary=""> -<tr><td class="l">Ca₃Al₂(SiO₄)₃ </td><td class="l">= grossularite</td></tr> -<tr><td class="l">Mg₃Al₂(SiO₄)₃ </td><td class="l">= pyrope</td></tr> -<tr><td class="l">Fe₃Al₂(SiO₄)₃ </td><td class="l">= almandite</td></tr> -<tr><td class="l">Mn₃Al₂(SiO₄)₃ </td><td class="l">= spessartite</td></tr> -<tr><td class="l">Ca₃Fe₂(SiO₄)₃ </td><td class="l">= andradite</td></tr> -<tr><td class="l">Ca₃Cr₂(SiO₄)₃ </td><td class="l">= uvarovite</td></tr> -</table> -<div class="pb" id="Page_123">123</div> -<p><b>Grossularite</b> is chiefly found in crystalline -limestones, which have resulted either from -contact with lavas, or from general metamorphism -of impure limestones. These garnets are -colorless to white, or more often shades of yellow, -orange, pink, green or brown, according to traces -of impurity which they may contain. The -cinnamon-colored variety from Ceylon is termed -<i>cinnamon stone</i>, and is a fairly popular gem.</p> -<p><b>Pyrope</b> is a deep-red color and when perfect -is highly prized as a gem. It is found in dark-colored -igneous rocks, like lavas, or serpentines. -Some of the finest come from South Africa, where -they are found in company with the diamond.</p> -<p><b>Almandite</b> is dark-red to brown in color, the -brownish-cast distinguishing it from pyrope. -It is one of the garnets known as “common garnet.” -In some cases it is clear and deep colored -enough to be used as a gem, but mostly it is -muddy in appearance. The name almandite -comes from Alabanda, a city of the ancient district -of Caria, Asia Minor, whence garnets were -traded to ancient Rome. The finest garnets -“Sirian garnets” came from the city of “Sirian” -in Lower Burma, and were supposed to have been -found near there, but careful investigation shows -that no garnets occurred near there, and this -town was therefore, even at that early time, a -distributing point for garnets, found probably -further to the east. The “Sirian” garnet had a -violet cast and now the term is used to indicate a -type of garnet, rather than a locality.</p> -<p><b>Spessartite</b> is dark-hyacinth-red, or red with a -violet-tinge, and is one of the less-common garnets. -<span class="pb" id="Page_124">124</span> -It is usually found in granites. The finest -garnets of the type come from Amelia Court -House, Va., which has yielded some ranging -from one up to a hundred carats.</p> -<p><b>Andradite</b> is another garnet which is termed -“common garnet.” It is red in color, but with a -yellowish-cast which distinguishes it from almandite, -but these two are not easy to separate. -It is found mostly in metamorphosed limestones. -One variety is black in color and called <i>malanite</i>. -It is found in lavas. The common yellowish-red -garnets are found through New England and the -Piedmont Plateau.</p> -<p><b>Uvarovite</b> is a rare garnet of emerald-green -color, found in association with chromium ores.</p> -<p>The number of localities for garnets is so great -that a list would suggest most of the regions -where metamorphic rocks occur, as all over New -England, throughout the Piedmont Plateau, the -Rocky Mountains, etc. Certain fine clear garnets, -found in Montana, northeastern Arizona, and -northwestern New Mexico are sold under the -trade name of “Montana, Arizona or New -Mexico rubies.” These are of fine quality and -are mostly collected by the Indians from the ant -hills and scorpion’s nests of those regions.</p> -<p>Garnets are among the earliest stones mentioned -in ancient languages, as would be expected -from the way these hard and beautiful -crystals weather out of the much softer metamorphic -rocks, like schists. In the past they, -with most any other translucent red stone, were -included under the name <i>carbuncle</i>. This, however, -is not the name of any mineral, but refers -<span class="pb" id="Page_125">125</span> -rather to a mode of cutting, <i>en cabochon</i> or with -a convex surface.</p> -<h3 class="center"><span class="sc">Glucinum</span></h3> -<p>Glucinum is a rare metal, silvery-white in -color, malleable, and melting at a fairly low -temperature. It is found in the mineral beryl, -from which has come the alternative name <i>beryllium</i>. -The name comes from the sweet taste of -its salts. Except for beryl its minerals are rare, -and the metal has found but few uses for man.</p> -<h3><a id="species_Beryl">Beryl</a> -<br />Gl₃Al₂(SiO₃)₆ -<br /><a href="#Plate_39">Pl. 39</a></h3> -<p>Occurs in hexagonal crystals in -granites, gneisses and mica schists; -hardness, 7.5; specific gravity, 2.7; -color usually some tint of green; luster vitreous; -transparent on thin edges.</p> -<p>When this mineral occurs in coarse hexagonal -prisms, with or without faces on the ends, it is -known as beryl; when the crystals are clear and -perfect and of a dark-green color, they are of gem -value and are termed <i>emerald</i>; when of a light-green -color, they are <i>aquamarine</i>; and when -bright-yellow in color, they are the <i>golden beryl</i>. -There is little difficulty in determining beryl, for -only apatite occurs in such crystals, and is green, -and this latter mineral has a hardness of only 5. -There is an imperfect basal cleavage.</p> -<p>Ordinary beryl is fairly common in granites of -the pegmatite sort, and less common in gneisses -and mica-schists. This type often furnishes -crystals of large size, up to two and three feet in -diameter.</p> -<div class="pb" id="Page_126">126</div> -<p>Beryl which is free from cracks and inclosures, -so it can be used as a gem, is so rare, that the -emerald has a value above that of the diamond, -and second only to the ruby. It is one of the -gems with a long history, having been quarried -on the west coast of the Red Sea at least 1650 -<span class="small">B.C.</span> by the Egyptians. To early people it had a -power to quicken the prophet instinct and made -the wearer see more clearly. The Spanish conquistadores -found fine emeralds among the treasures -of both Mexico and Peru. In the United -States, Stony Point, N. C., was a notable locality -for these gems, but now seems to have been exhausted. -The name emerald has been applied to -many other green stones, usually with some geographical -modification, as “Oriental emerald” -which is green corundum, “Brazilian emerald” -which is tourmaline, etc.</p> -<p>Giant beryls have been found at Acworth and -Grafton, N. H., and at Royalston, Mass. Localities -for ordinary beryl are Albany, Norway, -Bethel, Hebron, Paris, and Topsham, Me., Barre, -Goshen and Chesterfield, Mass., New Milford -and Branchville, Conn., Chester and Mineral -Hill, Penn., Stony Point, N. C., and many other -localities in the Appalachians; also Mount -Antero, Colo., and in the Black Hills of South -Dakota.</p> -<h3><a id="species_Sodalite">Sodalite</a> -<br />Na₄Al₃Cl(SiO₄)₃</h3> -<p>Occurs in irregular masses, sometimes -in dodecahedrons; hardness, -5.5-6; specific gravity, 2.3; color -deep-blue to colorless; streak white; luster vitreous; -translucent on thin edges.</p> -<div class="pb" id="Page_127">127</div> -<p>This striking mineral, with its deep-blue to -azure color, is not easily confused with any other. -It is characteristic of soda-rich igneous rocks -such as syenite and some lavas. In this country -it is found at Litchfield, Me., and Salem, Mass.</p> -<h3><a id="species_Zircon">Zircon</a> -<br />ZrSiO₄ -<br /><a href="#Plate_39">Pl. 39</a></h3> -<p>Usually occurs in tetrahedral crystals -in igneous rocks; hardness, 7.5; -specific gravity, 4.7; color brown; -luster vitreous; translucent on thin edges.</p> -<p>Zircon, the mineral of the rare earth element -zirconium, nearly always occurs in light-colored -igneous rocks, like syenite. It may occur in -schists or gneisses, but in these rocks the crystals -are of microscopic size. Because of their great -hardness and insolubility, zircon crystals resist -weathering and are often found, along with gold, -cassiterite, or magnetite, in sands which have -resulted from the disintegration of syenite rocks.</p> -<p>Zircon refracts and disperses light to a degree -second only to the diamond, so that clear crystals -are sought as gems. They are often called “Matura -diamonds” because of their abundance -at Matura, Ceylon. When the crystals are -colorless or smoky they are termed <i>jargons</i> or -<i>jargoons</i>; when of a red-orange hue, they are -<i>hyacinth</i> or <i>jacinth</i>. Most of the zircon of gem-quality -comes from Ceylon, where it is picked up -as rolled-pebbles from the beds of brooks.</p> -<p>The most remarkable American locality for -zircon is near Green River, in Henderson Co., -N. C., where it is found abundantly in a decomposed -pegmatite dike, from which many tons -have been obtained. It is also found at Moriah, -<span class="pb" id="Page_128">128</span> -Warwick, Amity and Diana, N. Y., at Franklin -Furnace, and Trenton, N. J., in the gold-bearing -sands of California, etc.</p> -<h3><a id="species_Cyanite">Cyanite</a> -<br />Al₂SiO₅ -<br /><a href="#Plate_40">Pl. 40</a></h3> -<p>Occurs in long blade-like crystals -in gneisses and schists; hardness, 7 -at right angles to the length, and -4.5 parallel to the length; specific gravity, 3.6; -color blue; luster vitreous; translucent on thin -edges.</p> -<p>There are only a few blue minerals, and the -way in which cyanite occurs in long thin blade-like -crystals is entirely characteristic. If more -is still wanted to determine this mineral, its -unique character in having the great hardness 7 -when scratched parallel to the length, and only -4.5 when scratched crossways, will settle any -doubts.</p> -<p>The mineral <i>sillimanite</i> has the same composition -as cyanite, but is fibrous in habit and has the -hardness 6.5. If cyanite is heated to 1350° C. -it changes its character and becomes sillimanite.</p> -<p>Cyanite is found as an accessory mineral in -metamorphic rocks, such as gneiss and schist, at -Chesterfield, Mass., Litchfield and Oxford, Conn., -in Chester Co., Penn., in North Carolina, etc.</p> -<h3 class="center"><span class="sc">The <a id="species_Mica">Mica</a> Group</span></h3> -<p>The micas are very common minerals, easily -recognized by their very perfect basal cleavage, -as a result of which thin sheets, often less than a -thousandth of an inch in thickness, readily split -off. These are tough and elastic, which distinguishes -<span class="pb" id="Page_129">129</span> -mica from the chlorite group in which -there is similar basal cleavage, but the sheets are -not elastic.</p> -<p>Micas are complex silicates of aluminum, with -potassium, iron, lithium, magnesium and hydrogen. -They are one of the principle components -of many granites, gneisses, and schists. This -mineral is always crystalline, being in the monoclinic -system, but occurring in six-sided prisms. -The cleavage is so dominant a character that the -crystal form is usually overlooked, as it is seldom -requisite in determining this mineral. The size -of the sheets of mica depend on the size of the -crystals, the larger sheets expressing great slowness -in cooling from the original magmas. Sometimes -the crystals may be two or even three feet -in diameter. The hardness is not great, ranging -between 2 and 3. The specific gravity lies between -2.7 and 3.2. The color varies according to -the composition, from silvery-white, through -gray, pink, and green to black. The luster is -vitreous to pearly, sometimes gleaming in the -darker-colored varieties. The commoner types -of mica are as follows:</p> -<dl class="undent"><dt>Muscovite, H₂KAl₃(SiO₄)₃ or potash mica.</dt> -<dt>Lepidolite, LiK(Al₂OH·F)Al(SiO₃)₃ or lithia mica.</dt> -<dt>Biotite, (HK)₂(MgFe)₂Al₂(SiO₄)₃ or iron mica.</dt> -<dt>Phlogopite, H₂KMg₃Al(SiO₈)₃ or magnesia mica.</dt></dl> -<p><b>Muscovite</b> is colorless, silvery-white, gray or -sometimes pale-green or brown. It gets its name -from Moscow where it was early used for window -<span class="pb" id="Page_130">130</span> -panes, and it is still used for stove and furnace -doors, as well as in electric work, for a lubricant, -etc.</p> -<p>The best crystals occur in granites, in the -coarse varieties of which large crystals may be -obtained. It is found also as small scales in -gneisses and schists, and when weathered from -its original rocks it may be present in sandstones -and shales. Muscovite is always in its origin an -elementary component of deep-seated igneous -rocks, like granite; but is never a component of -extruded lavas. <i>Sericite</i> is muscovite which has -been secondarily produced by the alteration of -other minerals into muscovite, as when feldspar, -cyanite, topaz, etc., have been modified by the -presence of heat and hot vapors, when near lavas -that have come in contact with other rocks. -Muscovite is very resistant to alteration by -weathering, but when it does change, the greater -part of it becomes kaolin. It is found at Acworth -and Grafton, N. H., in plates, sometimes a yard -across at Paris, Me., Chesterfield and Goshen, -Mass., Portland and Middletown, Conn., at -Warwick, Edenville, etc., N. Y., and all down the -Appalachian Mts., also in the Rocky Mts., the -Cascade Range, etc.</p> -<p><b>Lepidolite</b> is pink or lilac in color and occurs in -scaly masses, mostly in granites. It does not -come in large crystals. Lepidolite is found -at Paris and Hebron, Me., Middletown, Conn., -Pala, Calif., etc.</p> -<p><b>Biotite</b> is dark-brown or black mica. Like -muscovite it is very common, making one of the -chief components of granites, gneisses and schists; -<span class="pb" id="Page_131">131</span> -and, unlike muscovite, it may occur in extrusive -lavas, like trachyte, andesite, and basalt. It -resists weathering much less than muscovite, so -that, when the rocks of which it is a component -disintegrate, biotite is usually altered to kaolin -and other compounds. It is likely to occur in -good-sized crystals, especially at Topsam, Me., -Moriah, N. Y., Easton, Penn., etc.</p> -<p><b>Phlogopite</b> is pale-brown, often coppery in -color, and is most likely to occur in serpentines, -or crystalline limestones or dolomites, often in -fine crystals, of good size. While one of the less -abundant micas, this is found at Gouverneur, -Edwards, and Warwick, N. Y., Newton, N. J., -and Burgess, Canada.</p> -<h3><a id="species_Topaz">Topaz</a> -<br />Al₂F₂SiO₄ -<br /><a href="#Plate_41">Pl. 41</a></h3> -<p>Occurs in crystals mostly; hardness, -8; specific gravity, 3.5; colorless -to pale-yellow; luster vitreous; -transparent on thin edges.</p> -<p>Topaz may be colorless, but is more often some -shade of yellow, and at times brown or even blue. -Its hardness is characteristic, there being but few -minerals as hard, and it is used to represent the -hardness 8 in the Moh’s scale. The crystals are -orthorhombic prisms, with the edges of the -prism beveled and often striated. The ends of -crystals usually terminate with a basal plane, -parallel to which there is good cleavage. Between -this basal plane and the prism faces there -are usually several sets of small faces as indicated -on <a href="#Plate_41">Plate 41</a>.</p> -<p>This mineral, as is also true of most minerals -containing fluorine, is one of those which have -<span class="pb" id="Page_132">132</span> -crystallized out from hot vapors, escaping from -igneous magmas. It is associated with such -minerals, as tourmaline, beryl, fluorite, and cassiterite, -and occurs mostly in cavities or seams, -in or near granites.</p> -<p>Ordinary topaz, which means crystals that are -imperfect by reason of tiny cracks and impurities -is not very rare, but crystals which are perfect -and clear in color are considered gems. Most of -the gem-topaz is some shade of yellow, but may -be brown or blue, never, however, pink, as is often -seen in jewelry. The “pinking” is artificial, and -done by packing yellow or brown topaz in magnesia, -asbestos, or lime, and then heating it -slowly to red heat, after which it is cooled slowly. -If underheated the color is salmon, if overheated -all color disappears. Topaz has been a gem for -centuries, the earliest records coming from Egypt. -The name comes from <i>topazios</i>, meaning to seek, -because the earliest known locality, from which -it was gathered, was a little island of that name -in the Red Sea, and this island was often surrounded -by fog and hard for those early mariners -to find. Here by mandate of the Egyptian kings -the inhabitants had to collect topazes, and deliver -them to the gem-cutters of Egypt for polishing.</p> -<p>Several yellow stones are called topaz, as the -“Oriental topaz” which is corundum and more -valuable than topaz itself; and several varieties of -yellow quartz, which go under such names as -“Saxon,” “Scotch,” “Spanish,” and “smoky” -topaz. When topaz occurs colorless as in Siberia, -the Ural Mountains, and in the state of Minas -<span class="pb" id="Page_133">133</span> -Geraes, Brazil, in all of which places it is found -as pebbles in brooks, it goes under the name of -“slave’s diamonds.” Brazil is today the chief -source of gem-quality topaz.</p> -<p>Ordinary topaz is found in this country at -Trumbull, Conn., Crowder’s Mt., N. C., Thomas -Mts., Utah, in Colorado, Missouri, and California, -etc.</p> -<h3><a id="species_Staurolite">Staurolite</a> -<br />FeAl₅OH(SiO₆)₂ -<br /><a href="#Plate_41">Pl. 41</a></h3> -<p>Occurs in orthorhombic crystals; -hardness, 7.5; specific gravity, 3.7; -color brown; luster resinous; translucent -on thin edges.</p> -<p>This mineral occurs about equally abundantly -in simple crystals similar to the outline on <a href="#Plate_41">Plate 41</a>, -and in twins which have grown through each -other either at 90° or at 60°. The color is either -brown or reddish-brown. In all cases it is an -accessory mineral, occurring in metamorphic -rocks, usually schists, though less frequently -in slates and gneisses.</p> -<p>From the seventeenth century on, it has been -used as a baptismal stone, and worn as a charm, -legends stating that it fell from the heavens. -Fine crystals have been found in Patrick County, -Va., and there is in this region the legend, that -when the fairies heard of the crucifixion of Christ, -they wept and their tears falling crystallized in -the form of crosses, such as the one shown on -<a href="#Plate_41">Plate 41</a>.</p> -<p>Staurolite is found in the schists of New England -as at Windham, Me., or Chesterfield, Mass., -and all down the east side of the Appalachian -Mountains to Georgia.</p> -<div class="pb" id="Page_134">134</div> -<h3><a id="species_Olivine">Olivine</a> -<br />(MgFe)₂SiO₄ -<br /><i>Peridot</i> or <i>Chrysolite</i></h3> -<p>Occurs in grains and irregular -masses in dark lavas; hardness 6.5 -to 7; specific gravity 3.3; color -bottle- to olive-green; luster vitreous; -translucent on thin edges.</p> -<p>Olivine rarely occurs in crystals, but when it -does they belong to the orthorhombic system. -The dark-green grains or masses are recognized -by the color, considerable hardness and indistinct -cleavage. Serpentine may have a similar -color, but its hardness is only 4. In hydrochloric -acid olivine decomposes to a gelatinous mass.</p> -<p>Olivine is typically one of the constituents of -the dark lavas, like basalt, gabbro, or peridotite. -It is also a common mineral in meteorites. -Olivine, in the presence of water, alters to -other minerals, especially serpentine, with great -facility.</p> -<p>It occurs fairly widely wherever the dark lavas -are present, as in the White Mountains of N. H., -in Loudoun Co., Va., in Lancaster Co., Penn., -and in many localities in the Rocky Mountains -and Cascade Range.</p> -<h3><a id="species_Epidote">Epidote</a> -<br />Ca₂(AlOH)(AlFe₂)(SiO₄)₃ -<br /><a href="#Plate_42">Pl. 42</a></h3> -<p>Occurs in grains or columnar -masses; hardness, 6.5; specific gravity -3.4; color green, usually a -pistachio or yellow-green; luster -vitreous; translucent on thin edges.</p> -<p>Rarely epidote occurs in crystals, which belong -to the monoclinic system, and may be either -short like the diagrams on <a href="#Plate_42">plate 42</a> or long and -needle-like. The color and hardness will suffice -to determine this mineral, as almost no other has -<span class="pb" id="Page_135">135</span> -the peculiar yellowish-green color which is -characteristic of this form.</p> -<p>Epidote occurs primarily in metamorphic -rocks at or near the contact with igneous rocks; -or it may be a secondary mineral resulting from -the weathering of granites, especially along seams. -It sometimes occurs with hornblende in highly -folded schists, as in New York City. It is often -a mineral which has resulted from the alteration -of other minerals, as pyroxene, amphibole, -biotite, or even feldspars.</p> -<p>It is found at Chester and Athol, Mass., -Haddam, Conn., Amity, Munroe and Warwick, -N.Y., East Branch, Penn., in the Lake Superior -region, in the Rocky Mountains, etc.</p> -<h3><a id="species_Tourmaline">Tourmaline</a> -<br />(FeCrNaKLi)₄Mg₁₂B₆Al₁₆H₈Si₁₂O₆₃ -<br /><a href="#Plate_42">Pl. 42</a> & <a href="#Plate_Frontispiece">frontispiece</a></h3> -<p>Occurs in three-sided prismatic -crystals; hardness, 7; specific gravity, -3.1; colorless, red, green, brown, -or black; luster vitreous; transparent -on thin edges.</p> -<p>Tourmaline is readily distinguished -from other minerals, as it -always occurs in long to short prisms, which are -three-sided in cross section. There is also a -tendency for the sides to be curved as seen on -the end view of D, <a href="#Plate_42">Pl. 42</a>. Frequently the vertical -edges of the prism are beveled with one, two -or three faces, grouped about each of the three -original edges, and there are often striations on -the prism faces. The ends are terminated by a -low rhombohedron and again there may be a -host of modifying faces on the edges and corners -of the end. The common varieties are brown or -<span class="pb" id="Page_136">136</span> -black in color, but occasionally there may occur -green, red, yellow or almost any color. When -the crystals are perfect, that is free from impurities -and without tiny cracks, tourmaline becomes -a gem of popularity and value.</p> -<p>Tourmaline is very complex in composition -and may vary considerably, the sodium, potassium, -lithium, magnesium, and iron being either -more or less abundant or even lacking. The color -is to some extent dependent on the proportions -of these elements present, the dark varieties -having more iron, and the light colored tourmalines -lacking it. This mineral is one of those -which form from superheated vapors, escaping -from molten magmas. It will therefore occur in -veins, often associated with copper minerals, in -crystalline limestones, or in cavities in granites, -where it is associated with such minerals, as -beryl, apatite, fluorite, topaz, etc.</p> -<p>If heated tourmaline crystals develop electricity, -with the effect of making one end a positive -and the other a negative pole, and then will attract -bits of straw, ashes, etc. It was first introduced -into Europe about 1703 from India, and -its vogue as a gem has greatly increased since it -was found on Mount Mica near Paris, Me. This -Paris, Me., locality was discovered by two boys, -amateur mineralogists, Elijah L. Hamlin and -Ezekiel Holmes, who in 1820 were returning -home from a trip hunting for minerals, when, at -the root of a tree, they discovered some gleaming -green substance. It proved to be gem-quality -tourmaline. A snow storm that night buried -their “claim,” but next spring it was visited and -<span class="pb" id="Page_137">137</span> -several fine crystals found. Later this locality -was systematically worked, and over $50,000 -worth of tourmaline taken from the pegmatite -seam in the granite, which lay under the crystals -found on the surface. The figure in the <a href="#Plate_Frontispiece">frontispiece</a> -is one of the crystals from there.</p> -<p>Well known localities are Paris and Hebron, -Me., Goshen and Chesterfield, Mass., Acworth -and Grafton, N. H., Haddam and Munroe, -Conn., Edenville and Port Henry, N. Y., Jefferson -Co., Colo., San Diego Co., Calif., etc.</p> -<h3><a id="species_Kaolinite">Kaolinite</a> -<br />H₄Al₂Si₂O₉ -<br /><i>Kaolin</i></h3> -<p>Usually found in whitish clay-like -masses; hardness, 2; specific -gravity, 2.6; color white to grayish -or yellowish; luster dull.</p> -<p>Kaolinite does not generally occur in crystals, -though crystals of microscopic size and monoclinic -forms have been found. It is a secondary -mineral resulting from the decomposition by -weathering of feldspars, the calcium, potassium -or sodium having been replaced by water. When -found in place it is generally white or nearly -white, and is characterized by its greasy feel.</p> -<p>As granites or other feldspar-bearing rocks are -weathered away, the kaolin is washed out by -water, and with other fine material is carried -down into lakes or the sea, where it settles to the -bottom and is known as clay. Clay is kaolin -with more or less impurities.</p> -<p>Pure kaolin is used for the manufacture of -china and white porcelain ware; but when it is -impure, especially when it has iron in it, baking -causes the product to turn red or brown, so -<span class="pb" id="Page_138">138</span> -that it is only suitable for making tile, bricks, -etc.</p> -<p>It is found almost anywhere that feldspar -rocks are, or have been, exposed to weathering.</p> -<h3><a id="species_Talc">Talc</a> -<br />H₂Mg₃(SiO₃)₄</h3> -<p>Occurs in scales, or in fibrous, -scaly or compact masses; hardness, -1; specific gravity, 2.7; color white, -gray or pale-green; luster pearly; translucent on -thin edges.</p> -<p>This mineral is as soft as any, only graphite -and molybdenite being of the same hardness, but -both these latter two have a black streak, while -the streak of talc is white. The greasy feel is -also characteristic. Talc is very seldom found in -crystals, but if they are found, they will appear like -flakes and have a hexagonal cross section, though -in reality they belong to the monoclinic system.</p> -<p>Talc is a secondary mineral which usually -results from the exposure of magnesium silicates, -such as pyroxenes or amphiboles, to moisture. -In this case, in-as-much as the original rocks were -metamorphic in origin, the talc therefrom will -occur in old metamorphic regions. Some talc is -also formed by the action of silica-bearing waters -on dolomite. This is likely to be the case near -the contact between dolomite and igneous rocks. -Talc is closely related to serpentine and likely -to be found in the same regions.</p> -<p>Talc has come to have a considerable use. -Some of it is compact and then called soapstone, -and this was used by the ancient Chinese to make -images and ornaments; and our North American -Indians used it to make large pots, to serve as -<span class="pb" id="Page_139">139</span> -containers for liquids. Some of these pots have -been carved out with great skill, so as to be fairly -light in proportion to what they would hold. -Pipes and images were also carved from soapstone. -Today we still cut soapstone into slabs -to make mantels, laundry tubs and sinks. The -scaly and fibrous varieties are ground, and used -in making paper, paint, roofing, rubber, soap, -crayons, toilet powders, etc. The United States -produce and use over half the world’s production, -our industries requiring over 100,000 tons of talc -a year. Of this 38% goes into paper, 23% into -paint, 18% into roofing, and so on down to toilet -powder which uses 2½%, or 2,500 tons a year.</p> -<p>Talc is found in metamorphosed regions, that -is in New England, all down the east side of the -Appalachian Mts., in the Rocky Mts., and the -Cascade Ranges, with a large number of local -occurrences. New York State is the leading producer.</p> -<h3><a id="species_Serpentine">Serpentine</a> -<br />H₄Mg₃Si₂O₉ -<br /><a href="#Plate_43">Pl. 43</a></h3> -<p>Occurs in compact, granular or -fibrous masses; hardness, 3; specific -gravity, 2.6; color green; luster -greasy; translucent on thin edges. Serpentine -is never in crystals. Its color and hardness -serve to distinguish it. Like talc it is a secondary -mineral resulting from the alteration, in -the presence of moisture, of pyroxenes, amphiboles, -and especially, olivine. As these are often -in metamorphic rocks, the serpentine is likely to -be associated with metamorphic rocks. Some -serpentine is also the result of the action of silica-bearing -water on dolomite, and this is likely to -<span class="pb" id="Page_140">140</span> -occur in areas of sedimentary rocks. The fibrous -variety of serpentine, <i>chrysolite</i>, usually occurs in -seams or veins, and when the fibers are long, it is -used as asbestos. This form of asbestos is the -one most used commercially today, as there are -remarkably large deposits of it in the Province of -Quebec, which provide the major part of the -world supply. In the United States it is also -found in California and Arizona but only in -moderate quantities.</p> -<p>Massive serpentine is used in considerable -quantities as an ornamental stone, the green -color varied with streaks and blotches of white, -yellow and red, due to various impurities, making -it very effective. It is, however, only suitable -for interior work as the weather quickly spoils -the polished surface. This is further discussed -under serpentine rock, <a href="#Page_245">page 245</a>.</p> -<p>Serpentine is found at Newfane, Vt., Newburyport, -Mass., Brewster, Antwerp, etc., N. Y., -Hoboken, N. J., in Pennsylvania, Maryland, etc.</p> -<h3><a id="species_Chlorite">Chlorite</a> -<br />H₈(MgFe)₅Al₂(SiO₆)₃ -<br /><a href="#Plate_43">Pl. 43</a></h3> -<p>Occurs in monoclinic crystals of -six-sided outline, or in scaly flakes -or masses; hardness, 2; specific -gravity 2.8; color green; luster pearly -on cleavage faces; translucent on thin edges.</p> -<p>Chlorite is a family name, covering a series of -closely related minerals, so similar in appearance -that they are best considered under this common -name. In many respects they resemble mica, in -the shape of the crystals and the remarkable -basal cleavage. At first glance it is easy to confuse -the two, but chlorite scales are not elastic, -<span class="pb" id="Page_141">141</span> -and when bent, stay bent, instead of snapping -back like mica. In fact they look like more or -less rotted micas. This is more than appearance, -for chlorites form as a result of the alteration of -micas in the presence of moisture. They are -then secondary, and will be found where mica-rocks -have been weathered, as in granites and -schists.</p> -<p>They may be expected anywhere that micas -have been long exposed, as in New England, the -Rocky Mountains, or the Sierra Nevada or Cascade -Ranges. Special localities are Brewster, -N. Y., Unionville and Texas, Penn., etc.</p> -<h3 class="center"><span class="sc">The Zeolites</span></h3> -<p>The zeolites are a group of white minerals, -with a pearly luster, light weight, and easy solubility -in acids; which, because their contained -water is lightly held, readily boil before the blowpipe. -They are all secondary minerals, which -result from the decomposition of feldspars, when -exposed to weathering. They are almost universally -found in seams and cavities of disintegrating -lavas. From a group of a dozen or so, -three are common enough to be considered here. -They may be found by watching such places, as -where trap rock is being quarried for road material, -or being blasted for any reason.</p> -<h3><a id="species_Analcite">Analcite</a> -<br />Na₃Al₂Si₄O₁₃ + 2H₂O -<br /><a href="#Plate_44">Pl. 44</a></h3> -<p>Occurs as trapezohedrons in seams -and cavities in lavas; hardness, 5.5; -specific gravity, 2.2; colorless, white -or pink; luster vitreous; transparent -on thin edges.</p> -<div class="pb" id="Page_142">142</div> -<p>Analcite usually occurs in the 24-sided form, -known as a trapezohedron, as illustrated in figure -A, <a href="#Plate_44">Pl. 44</a>; but it may also occur in cubes with the -three faces of the trapezohedron on each corner. -Small crystals are often colorless, but the larger -ones are either white or pink, and are opaque. -While the form is the same as that of garnets, the -color, lesser hardness, and the occurrence in -lavas will serve to distinguish this mineral. If -placed in hydrochloric acid analcite dissolves -to a gelatinous mass.</p> -<p>It is always found in seams and cavities in -lavas, as at Bergen Hill and Weehawken, N. J., -Westfield, Mass., in the Lake Superior region, etc.</p> -<h3><a id="species_Natrolite">Natrolite</a> -<br />Na₂Al₂Si₃O₁₀ + 2H₂O -<br /><a href="#Plate_44">Plate 44</a></h3> -<p>Occurs as bristling crystals in -seams and cavities in lavas; hardness, -5.5; specific gravity, 2.2; colorless; -luster vitreous; transparent on -thin edges.</p> -<p>Natrolite occurs as beautiful bristling tufts of -needle-like crystals, each crystal an orthorhombic -prism with a very low pyramid on the end. -This mineral is so easily fusible that it can be -melted in a candle flame, giving to the flame the -characteristic yellow color due to sodium. In -hydrochloric acid it dissolves to a gelatinous -mass. It is always a secondary mineral in cavities -and seams in disintegrating lavas, and the -tuft-like manner of growth is so characteristic, -that once seen, it will always be recognized.</p> -<p>Natrolite is found at Weehawken and Bergen -Hill, N. J., at Westfield, Mass., in the Lake -Superior region, etc.</p> -<div class="pb" id="Page_143">143</div> -<h3><a id="species_Stilbite">Stilbite</a> -<br />H₄(CaNa₂)Al₂(SiO₃)₆ + 4H₂O -<br /><a href="#Plate_44">Pl. 44</a></h3> -<p>Usually occurs in sheaf-like -bundles of fibrous crystals; hardness, -5.5; specific gravity 2.2; colorless -to white, yellow or brown; luster -vitreous; transparent on thin edges.</p> -<p>Stilbite crystals are really monoclinic, but on -account of almost universal twinning, appear as -if orthorhombic. Like the two foregoing minerals, -stilbite is found in the seams and cavities of -disintegrating lavas. It is readily recognized by -its habit of forming in sheaf-like bundles of -fibrous crystals. It may also, but more rarely, -occur in radiating masses. In hydrochloric acid -it is completely dissolved. It is found in lavas, -at Weehawken and Bergen Hill, N. J., in the -Lake Superior region, etc.</p> -<h3 class="center"><span class="sc">Calcium</span></h3> -<p>Calcium is one of the most abundant of metals, -but never occurs as such in nature, nor is it used -as a metal by man. In its metallic form it is -yellowish-white, and intermediate between lead -and gold in hardness. Exposed to air it soon -tarnishes by oxidation, and in water rapidly decomposes -the water, forming the oxide. However, -it has a great affinity for other elements, -and makes a large number of minerals, the most -important of which are calcite, aragonite, gypsum -and fluorite, while it is an essential component -of some garnets, anorthite, epidote, amphibole -and pyroxene. It is very widely distributed -as limestone, and is found in solution in most all -natural waters, and in the shells and bones of -many animals and some plants.</p> -<div class="pb" id="Page_144">144</div> -<h3><a id="species_Calcite">Calcite</a> -<br />CaCO₃ -<br /><a href="#Plate_45">Pl. 45</a></h3> -<p>Occurs in well defined crystals -in incrustations, and in stalactitic, -oolitic, and granular masses; hardness, -3; specific gravity 2.7; colorless to white, or -when impure, yellow, brown, green, red or blue; -luster vitreous to dull; transparent on thin -edges.</p> -<p>Next to quartz, calcite is the most abundant of -all minerals, and occurs in an almost endless -variety of forms, over 300 having been described. -It belongs to the hemihedral section of the hexagonal -system, the form of the crystals being all -sorts of variations of the rhombohedron, and -combinations of left and right handed rhombohedrons. -The cleavage is entirely uniform, in three -directions, parallel to the faces of the rhombohedron, -and at an angle of 74° 55′ with each other. -Crystals may occur in the form characteristic of -the cleavage, but not often. The commonest -forms are a more or less elongated scalenohedron, -made by combining right and left handed rhombohedrons, -so that the resulting pyramid is six-sided, -as in figure C, <a href="#Plate_45">Plate 45</a>. Such a scalenohedron -may be combined with other forms in a -great variety of ways. The six-sided prism with -the ends terminated by one or more sets of -rhombohedral faces is also fairly common. -Twinning occurs occasionally.</p> -<p>The quickest way to determine calcite is by -the hardness (3), combined with the fact that it -effervesces, when hydrochloric acid is dropped -upon it.</p> -<p>An interesting feature of this mineral is its -marked property of deflecting light rays, so that -<span class="pb" id="Page_145">145</span> -a line or object placed behind a piece of clear -calcite appears double. It was with pieces of -calcite from Iceland that this was first seen; so -that large transparent crystals of calcite are still -called <i>Iceland spar</i>; and such calcite is used to -make the Nichol’s prisms for microscopes, which -are so useful in the study of minerals. This -power of refracting light is present in all minerals, -but not to such a marked degree as in calcite. -The elongated scalenohedrons of calcite are often -called “dog-toothed spar” from a fancied resemblance -between them and the dog’s tooth.</p> -<p>Calcite is present in solution in the water of -the sea and most streams, from which it is withdrawn -by many animals and some plants, to -make their shells, and bones. The foraminifera, -some sponges, the echinoderms, corals and molluscs -all draw large quantities from the water in -which they live, and build more or less permanent -structures from it. These shells when they fall -to the bottom, or after being broken to bits, -accumulate on the bottom and make limestone, -which is widely distributed over the country. -This same limestone, when metamorphosed and -crystalline, is marble.</p> -<p>Calcite then is readily soluble in water, and -streams flowing along crevices and fissures in -limestone dissolve out great cavities or caves, -like the Mammoth Cave of Kentucky. Other -water, percolating through the limestone, comes -to these cavities saturated with lime in solution -and drips from the roofs and walls; then as part -of the water evaporates, it deposits part of its -lime in icicle-like masses, hanging from the roof. -<span class="pb" id="Page_146">146</span> -Such masses of non-crystalline calcite are called -<i>stalactites</i>. Below on the floor of the cave, conical -masses are built up in the same manner where the -dripping water falls on the floor. These are -<i>stalagmites</i>. In these limestone caves and in -smaller cavities many of the most beautiful -crystals grow. Somewhat similarly, when hot -water from deep springs comes to the surface, -it cools and can not carry as much lime, and so -around the spring is laid down layer after layer -of non-crystalline calcite making a mass known -as <i>travertine</i>. Sometimes this is colored by iron -or other impurities and a banded effect results. -Such travertine as the “Suisun marble” from -California, “California onyx,” “Mexican onyx,” -and “satin spar” all belong to this class.</p> -<p>The coral animals, especially in tropical waters -precipitate an enormous amount of lime, until -whole reefs are built of lime in this non-crystalline -form. In places it is hundreds of feet thick -and hundreds of miles in extent. Some of this -coral has become popular for personal adornment. -This is particularly a small, fine-grained -variety, <i>Corallum rubrum</i>, which lives almost -exclusively in the Mediterranean Sea. This coral -is red in color, varying all the way from a deep -red to white. It grows in small masses, three -pounds being a good sized mass, in water 60 -to 100 feet deep, requires some ten years to -develop a full-sized mass. The making of this -into beads and ornaments is an Italian industry. -The demand is growing, while at the same time -the supply is diminishing, and search is being -widely made for more such coral, but up to the -<span class="pb" id="Page_147">147</span> -present time with little success. This precious -coral is much worn as a protection against the -“evil eye” and is widely imitated, apparently -with as much protection to the wearer. When -coral beads are offered cheap, they are probably -something else, red gypsum being much used. -This and all imitations can be readily detected by -trying a drop of acid in the bead. Coral will effervesce, -but gypsum and other substitutes will not.</p> -<p>The bulk of the shells of most molluscs is made -of lime, but the mother-of-pearl layer inside is -usually aragonite. The chalk of the cliffs on -either side of the English channel is lime, and -composed of the shells of single celled animals. -See <a href="#Page_213">p. 213</a>. When lime is deposited in loose porous -masses, as around grass, etc., and below hot -springs, this mass is termed <i>calcareous tufa</i>.</p> -<p>Calcite will be found almost everywhere, some -of the localities for the finest crystals being Antwerp -and Lockport, N. Y., Middletown, Conn., -the caves of Kentucky, Warsaw, Ill., Joplin, Mo., -Hazel Green, Wis., etc.</p> -<h3><a id="species_Aragonite">Aragonite</a> -<br />CaCO₃ -<br /><a href="#Plate_46">Pl. 46</a></h3> -<p>Occurs in crystals, in columnar or -fibrous masses, or incrustations; -hardness, 3.5; specific gravity, 2.9; -colorless, white or amber; luster vitreous; transparent -on thin edges.</p> -<p>Aragonite has the same chemical composition -as calcite, but it crystallizes in the orthorhombic -system, either in simple forms like A on <a href="#Plate_46">Plate 46</a>, -or twinned, so as to make forms which seem hexagonal. -When in simple crystals its form easily -distinguishes it from calcite and dolomite, but -<span class="pb" id="Page_148">148</span> -when twinned it appears much like either of -these two minerals. From calcite it can then be -distinguished by its greater hardness and the fact -that it has cleavage in one direction only, and -that imperfect. The cleavage is the only easy -method of distinguishing it from dolomite. However, -aragonite is most always easily distinguished -by its habits, for it generally forms long -slender crystals, which appear more like fibers -than crystals. Neither calcite nor dolomite is at -all fibrous.</p> -<p>Aragonite is much less abundant than calcite, -and has resulted, either from deposition from hot -waters, or from waters having sulphates in solution -as well as lime. Much of the travertine, and -many stalagmites and stalactites are composed -of aragonites, forming as outlined under calcite. -The mother-of-pearl layer in the shells of bivalves -is generally aragonite. The pearly luster of this -layer is due to its being formed by the successive -deposition of one thin layer upon another; so -that light falling on the mother-of-pearl, penetrates, -part of it to one layer and part to another, -and is then reflected. Certain molluscs have this -layer composed of especially thin layers, one, the -<i>Unios</i> or freshwater clams, the other, the “pearl -oysters” or <i>Aviculidæ</i>, these latter, however, -being only distantly related to the edible oysters. -In the cases, where molluscs of either of these two -families are of large size, large pieces of mother-of-pearl -can be recovered, and are used for buttons, -handles, and various ornamental objects. -A further peculiarity of these same molluscs is -the formation of pearls in the sheet of flesh, lining -<span class="pb" id="Page_149">149</span> -the shells. The pearls are round or rounded -concretions of aragonite. At the center there is -a grain of sand, or more often a tiny dead parasite. -Either was an irritant to the mollusc, and -to be rid of it, a layer of aragonite was secreted -around it. Then as the mollusc continued to -grow and secrete layers for its shell, it also added -each time another layer around the sand-grain -or parasite, until in time a pearl of noticeable, -and then of considerable size resulted. These -have all the pearly luster of the mother-of-pearl -in a sphere which tends to make the luster even -more marked.</p> -<p>Pearls were in use as ornaments in China some -twenty-three centuries before Christ, and in -India over 500 <span class="small">B.C.</span> They were very highly -prized by the Romans and since their times the -rulers of India have shown a remarkable fondness -for them. Today the finest come from the -Gulf of Persia and the Red Sea, while still -others are found about Australia and in the -Caribbean Sea. In the United States not a few -are collected every year from the fresh water -clams, some of them beautifully tinted with -pink or yellow.</p> -<p>Aragonite is found widely, as at Haddam, -Conn., Edenville, N. Y., Hoboken, N. J., New -Garden, Penn., Warsaw, Ill., etc.</p> -<h3><a id="species_Anhydrite">Anhydrite</a> -<br />CaSO₄ -<br /><a href="#Plate_46">Pl. 46</a></h3> -<p>Occurs in cleavable or granular -masses, rarely in crystals; hardness, -3-3.5; specific gravity, 2.9; color -white, gray, bluish or reddish; luster pearly on -cleavage faces; transparent on thin edges.</p> -<div class="pb" id="Page_150">150</div> -<p>When anhydrite occurs in crystals, they are -orthorhombic, like the diagram on <a href="#Plate_46">Plate 46</a>. -Usually, however, it is found in beds or layers, -which were deposited by the evaporation of sea -water, and so it is associated with salt. Anhydrite -has three cleavage planes which are at right -angles to one another, which produce rectangular -or cube-like forms. Mostly anhydrite is associated -with gypsum, from which it differs by its -greater hardness, pseudo-cubic cleavage, and the -fact that anhydrite is not readily soluble in acid, -while gypsum is. Chemically it differs from gypsum -in not having water of crystallization, which -gypsum does have. The anhydrite is likely to -occur as veins and irregular masses in beds of -gypsum. Calcium sulphate is precipitated from -sea water when 37% of the water has been evaporated, -and it may be deposited either as anhydrite -or as gypsum, the factors, which decide -as to which of these two minerals it will be, being -as yet unknown. After deposition, if exposed to -moisture, the anhydrite may change to gypsum, -irregular masses often remaining unchanged.</p> -<p>It is found in salt mines in Elsworth Co., Kan., -in limestone cavities at Lockport, N. Y., in veins -in Shasta Co., Calif., etc.</p> -<h3><a id="species_Gypsum">Gypsum</a> -<br />CaSO₄ + 2H₂O -<br /><a href="#Plate_47">Pl. 47</a></h3> -<p>Occurs in crystals, in cleavable -masses, or in fibrous masses; hardness, -2; specific gravity, 2.3; colorless, -white, amber, gray, or pink; -luster vitreous, silky or pearly; transparent on -thin edges.</p> -<p>Gypsum crystals are monoclinic as seen on -<span class="pb" id="Page_151">151</span> -<a href="#Plate_47">Plate 47</a>, the perfect ones usually occurring in -clay, as at Oxford, O., or in cavities; while crystals -of less perfect outline, but with fine cleavages, -are found in Utah, Kansas, and Colorado. -The cleavage is very perfect in one direction, -making it possible to strip off thin sheets almost -like mica, and less perfect in two other directions, -which appear on the smooth surface of the first -cleavage as lines intersecting at 66° 14′. Twinning -is also common in such a way, that the two -united crystals make forms similar to arrowheads. -These cleavages and the twinning show -nicely in the photograph of gypsum on <a href="#Plate_47">Plate 47</a>.</p> -<p>Gypsum is distinguished from anhydrite by its -lesser hardness, its cleavage and by being soluble -in acids.</p> -<p>Most gypsum occurs in beds or granular -masses which were deposited from evaporating -sea-water, coming down when 37% of the water -was lost. Such beds are often very extensive and -are quarried as a source of gypsum to make plaster -of Paris, stucco, neat plaster, Keene’s cement, -plaster and wall board, partition tiles, etc. The -use of the gypsum for plaster of Paris and all -these other uses is based on its affinity for water -of crystallization. The gypsum is first heated to -about 400° C., which drives off the water of crystallization, -and causes it to crumble to a powder, -which is the plaster of Paris. When water is -added, it is taken up and the powder “sets,” or -recrystallizes back to gypsum. This simple -reaction has made it very useful, for making -moulds, casts, hard finish on walls, as stucco, etc.</p> -<p>When the granular type of gypsum is fine -<span class="pb" id="Page_152">152</span> -grained, it is known as <i>alabaster</i>, which is used for -carving vases, statuettes, ornaments, etc. The -fibrous variety is called <i>satin spar</i>, and is sometimes -used for cheap jewelry and ornaments, but -it is very soft and quickly wears out. At Niagara -Falls there is a considerable trade in objects -carved from this satin spar, tourists buying them -on the assumption that the mineral is native and -comes from under the falls. Most of it, however, -comes from Wales, the small amount of gypsum -of that region being mostly granular.</p> -<p>Gypsum is found all across the United States, -as in New York, Michigan, Virginia, Ohio, Alabama, -South Dakota, Wyoming, Colorado, -Utah, California, etc.</p> -<h3 class="center"><span class="sc">The Strontium Group</span></h3> -<p>Strontium is a pale-yellow metal, ductile and -malleable, but oxidizing quickly when exposed -to the air. It does not occur in its native state -in Nature, but always as some compound, usually -either the carbonate or sulphate. It resembles -barium, but differs in giving to the -flame a brilliant red color, on which account the -compounds of strontium are used mostly in -making red fire in fireworks.</p> -<h3><a id="species_Strontianite">Strontianite</a> -<br />SrCO₃</h3> -<p>Occurs in needle-like crystals, or -in columnar or fibrous masses; hardness, -3.5-4; specific gravity, 3.6; -color white, pale-green or pale shades of yellow; -luster vitreous; transparent on thin edges.</p> -<p>Strontianite is orthorhombic, but appears as -if hexagonal, since its general habit is to have -<span class="pb" id="Page_153">153</span> -three twin crystals grow together in such a way -as to make a six-sided double pyramid. In this -it is very like witherite, both these minerals appearing -externally much alike. They can be -readily distinguished, however, by holding a -piece in the flame. If it gives a red color to the -flame it is strontianite, if green, it is witherite. -It effervesces readily in hydrochloric acid.</p> -<p>Strontianite is found in veins and cavities in -limestone, where it has been deposited after -being leached from the limestone by percolating -waters. Though known at several localities it is -not now being mined in this country, what we -use being imported mostly from Germany.</p> -<p>It is found at Schoharie, Chaumont Bay and -Theresa, N. Y., in Mifflin Co., Penn., etc.</p> -<h3><a id="species_Celestite">Celestite</a> -<br />SrSO₄</h3> -<p>Occurs in crystals, cleavable -masses and fibrous; hardness, 3; -specific gravity, 3.9; colorless, white, -pale-blue, or reddish; luster vitreous; transparent -on thin edges.</p> -<p>Celestite, the sulphate of strontium, is very like -barite in external appearance and habit. It is -orthorhombic and occurs in tabular crystals. -Its cleavage is perfect on the basal plane, and -imperfect in one other direction. The ready way -of distinguishing celestite from barite is to hold a -piece in the flame. If it is celestite it will color -the flame red, if barite, green.</p> -<p>Celestite is mostly found in veins or cavities in -limestone, where it has been deposited by percolating -waters, after having been leached from -the limestone. Some years ago an important -<span class="pb" id="Page_154">154</span> -deposit of celestite was found on Strontian Island -in Lake Erie, but that was soon worked out and -now no veins are being worked in this country. -It is also found at Chaumont Bay, Schoharie -and Lockport, N. Y., in Kansas, Texas, West -Virginia, Tennessee, etc.</p> -<h3 class="center"><span class="sc">The Barium Group</span></h3> -<p>Barium is another metal which does not occur -in its native state in Nature. It has only been -isolated as a yellow powder, which, exposed to -air or water, soon changes to one of the oxides. -Both barium and its compounds are peculiar in -causing a green color, whenever exposed to the -flame. Two of its compounds are fairly abundant, -the sulphate, barite, and the carbonate, -witherite. The former is the more abundant and -has come to be fairly widely used, something -over 100,000 tons being annually consumed in the -United States, to make the body in flat finish -paints for interior work and light colors, for a -filler in rubber goods, linoleum, oil cloth, glazed paper, -and for a wide range of chemical compounds.</p> -<h3><a id="species_Barite">Barite</a> -<br />BaSO₄ -<br /><a href="#Plate_48">Pl. 48</a> -<br /><i>heavy spar</i></h3> -<p>Occurs in crystals or in lamellar, -nodular or granular masses; hardness -3; specific gravity, 4.5; colorless, -white or almost any color; luster -vitreous; transparent on thin edges.</p> -<p>Barite occurs in orthorhombic crystals, which -are tabular in form, and usually have the edges -beveled, as in figure A, <a href="#Plate_48">Plate 48</a>. There is cleavage -in three directions, a rather perfect basal -cleavage, and two less perfect cleavages, which -<span class="pb" id="Page_155">155</span> -are at right angles to the basal cleavage plane, -and intersect each other at 78°.</p> -<p>The tabular form, the cleavage, the heavy -weight, and the fact that a piece of barite put -into the flame colors it green, all serve to distinguish -this mineral.</p> -<p>Barite is a secondary mineral of aqueous origin, -which has been deposited in veins and cavities -in igneous, metamorphic, or sometimes sedimentary -rocks. It is most likely to occur in -veins in igneous or metamorphic rocks, the -barium having been dissolved from certain feldspars -and micas by percolating water, and then -redeposited in the fissures, as the water came into -them. If in sedimentary rocks, the barite veins -are usually in limestones. Barite is quite likely -to be a gangue mineral for the ores of lead.</p> -<p>It is found at Hatfield and Leverett, Mass., -Cheshire, Conn., Pillar Point, N. Y., Cartersville, -Ga., in Virginia, North Carolina, South -Carolina, Missouri, Kentucky, Tennessee, Alabama, -Illinois, Wisconsin, Nevada, California, -Alaska, etc.</p> -<h3><a id="species_Witherite">Witherite</a> -<br />BaCO₃ -<br /><a href="#Plate_48">Pl. 48</a></h3> -<p>Occurs in crystals, or in granular -or columnar masses; hardness, 3.5; -specific gravity, 4.3; color white to -gray; luster vitreous; translucent on thin edges.</p> -<p>Witherite is not an abundant mineral. Its -crystals are really orthorhombic, but they are -usually twinned, three crystals growing through -each other in such a manner that the resulting -crystal appears like a six-sided double pyramid, -similar to the one figured on <a href="#Plate_48">Plate 48</a>. The commonest -<span class="pb" id="Page_156">156</span> -mode of occurrence is in compact -masses. Witherite effervesces when cold acid is -dropped upon it, which, with its heavy weight, -and the green color it gives to the flame, serves -to distinguish the mineral. It is used for medicines, -in chemical industries, and a considerable -amount is made into rat poisons. The chief -locality for witherite is in northern England, -but in this country it is found along with barite, -especially at Lexington, Ky., and in Michigan.</p> -<h3 class="center"><span class="sc">Carbon</span></h3> -<p>Carbon is an element widely distributed in -nature, occasionally appearing in its elementary -form, as graphite or the diamond, but much more -important in its compounds. Small quantities -are present in the air as carbon dioxide, CO₂, immense -quantities occurring in the carbonate -minerals, which have been considered under their -respective metallic salts, as calcite, malachite, -siderite, cerrusite, smithsonite, witherite, etc., -and still other large quantities being represented -in organic compounds, which occur as rocks -under the heads of petroleum, coal, etc. The -occurrence of limestones, graphite, coal or petroleum -is always indicative of the activity of living -organisms, and in some cases is the only indication -of life in the earlier rocks.</p> -<h3><a id="species_Graphite">Graphite</a> -<br />C -<br /><i>Plumbago</i></h3> -<p>Occurs in hexagonal scales or -flakes, in layered masses, or earthy -lumps; hardness, 1; specific gravity, -2.1; color black or steel-gray; streak gray; luster -metallic; opaque on thin edges.</p> -<div class="pb" id="Page_157">157</div> -<p>Like the diamond graphite is pure carbon, but -in this case it is in non-crystalline form. It -occurs in both igneous and metamorphic rocks. -In the former case it is either in flakes in the rock, -or in veins, and has been derived directly from -the molten magmas, having either precipitated -in the hardening granite or lava, or having been -carried into the fissures and there precipitated -to make the veins of graphite. In either case -the graphite probably represents organic deposits -which have been melted into the igneous magma -at the time of its formation. Graphite may also -occur in metamorphic rocks, beds of coal or other -organic deposits being altered by the heat. Such -beds are often of considerable extent and economic -importance.</p> -<p>The extreme softness, greasy feel, and the -dark-gray streak readily distinguish graphite.</p> -<p>It is widely used in making crucibles and furnace -linings for foundries, lead pencils, paint, -lubricating powders, etc.</p> -<p>Graphite is found at Brandon, Vt., Sturbridge, -Mass., Ashford, Conn., in Essex, Warren and -Washington Cos., N. Y., Clay, Chilton and -Coosa Cos., Ala., Raton, N. M., Dillon, Mont., -etc.</p> -<h3><a id="species_Diamond">Diamond</a> -<br />C</h3> -<p>Occurs in octahedral crystals; -hardness, 10; specific gravity, 3.5; -colorless to yellow, brown, blue, etc., -luster adamantine; transparent on thin edges.</p> -<p>Like graphite the diamond is pure carbon, but -in this case in crystal form. It is the hardest of -all minerals, and as brilliant as any; so that in -<span class="pb" id="Page_158">158</span> -spite of being by no means the rarest, it may -easily be considered the most popular of all gems. -Tiny diamonds have been made artificially under -great heat and pressure; so that this mineral is -thought of as forming in Nature in dark igneous -lavas at great depths. The diamond has good -cleavage parallel to the octahedron faces, and, -in spite of some traditions to the contrary, is -brittle.</p> -<p>There are not many diamond localities, the -most famous being the Kimberley district of -South Africa, which produces many times as -many diamonds as all the others put together, -though all the time some are being found in -Borneo and Brazil. A very few have been found -in the United States, only one locality however -yielding them in the original matrix. That is at -Murfreesboro, Ark., where they are mined in a -disintegrating peridotite (a dark lava, mostly -peridot), which has been extruded through the -sedimentary rocks of that region. This matrix -is similar to the “blue earth,” the matrix of the -diamonds of South Africa, which occurs in -“pipes,” representing the necks of ancient volcanoes. -The American diamonds are of small -size, averaging considerably less than a third of -a carat in weight, which does not allow great -value to the individual diamonds.</p> -<p>From time to time, especially large diamonds -have been found in different parts of the world, -the largest being the Cullinan diamond, found -at the Premier Diamond Mine of South Africa. -It weighed 3025 carats or about a pound and a -quarter, and was valued at over $3,000,000. It -<span class="pb" id="Page_159">159</span> -was presented to King Edward VII, who had it -cut into 11 brilliants, four of which are larger -than any other diamond yet found. Other famous -diamonds, like the Kohinoor, 106 carats, -found in India in 1304; the Regent, 136 carats, -also found in India; the Orloff, 193 carats, set in -the eye of an Indian idol; the South Star, 125 -carats, the largest ever found in Brazil; the blue -Hope, etc., have in many cases romantic and -interesting stories woven about them.</p> -<p>Though for ages diamonds have been highly -prized gems, it is only in comparatively recent -times that cutting and polishing have been resorted -to, for the purpose of enhancing their -brilliancy. This is done by grinding reflecting -faces on the original stone, by the aid of discs of -iron or tin in which diamond dust has been embedded. -Diamond chips and cloudy or imperfect -diamonds are used for making tools for cutting -glass, rock drills, etc.</p> -<h3 class="center"><span class="sc">Phosphorus</span></h3> -<p>The element phosphorus at ordinary temperatures -is an almost colorless, faintly yellow, solid -substance of glistening appearance and waxy -consistency. In Nature it does not occur pure, -but always as one of its compounds. It is of -great importance to man for it is one of the essentials -for plant growth and also for the higher -animals, being required for the bones and to some -extent for nervous tissue. Originally it is found -in all the igneous rocks. Some of the phosphorus -is removed by solution and carried to other regions -<span class="pb" id="Page_160">160</span> -and to the sea. From this distribution it -comes into the sedimentary rocks, and, when -they are altered by heat, into the metamorphic -rocks. Thus it has a wide, though by no means -even, distribution. The soils formed by disintegration -of these rocks probably all have some -phosphorus in them; but where there is vigorous -plant growth, it soon tends to become exhausted, -and must be renewed. For this reason the use of -phosphates has become of prime importance in -Agriculture. The possession of beds of rock -carrying phosphorus has come to be of international -importance. The United States is particularly -fortunate in this respect, and produces -over 25% of the world’s supply of phosphates. -Most all the phosphorus is recovered either -from phosphate minerals, the most important -of which is apatite, or from the non-crystalline -and impure mixtures of phosphate minerals -and other substances, discussed under phosphate -rock.</p> -<h3><a id="species_Apatite">Apatite</a> -<br />Ca₅F(PO₄)₃ -<br /><a href="#Plate_49">Pl. 49</a></h3> -<p>Occurs in crystals, concretionary -nodules, or in bedded masses; hardness, -5; specific gravity, 3.2; color -reddish-brown or green, rarely white or colorless; -luster vitreous; translucent on thin -edges.</p> -<p>Apatite occurs in hexagonal prisms, usually -with the ends truncated by a basal plane, and -with one or more sets of pyramidal faces between -the prism and the basal plane. Crystals range in -size from tiny to over a foot in diameter. There -is but one cleavage and that is basal. The crystal -<span class="pb" id="Page_161">161</span> -form, cleavage, and hardness will easily -determine this mineral. Apatite is usually associated -with igneous or highly metamorphic -rocks, such as granites, gneisses, and crystalline -limestones. While the phosphoric acid of apatite -is highly desirable for use in fertilizers, the crystals -do not occur in sufficient abundance to -make them commercially available, and non-crystalline -phosphate rocks are resorted to for -this purpose.</p> -<p>Crystals of apatite are found at Norwich and -Bolton, Mass., Rossie and Edenville, N. Y., -Suckasunny and Hurdstown, N. J., Leiperville, -Penn., Wilmington, Del., etc. Templeton, Canada, -is perhaps the best known locality for fine -apatite.</p> -<h3><a id="species_Turquois">Turquois</a> -<br />H₅[Al(OH)₂]Cu(OH)(PO₄)₄</h3> -<p>Occurs in seams and incrustations; -hardness, 6; specific gravity, -2.7; color bluish-green; streak blue; -luster waxy; translucent to opaque on thin -edges.</p> -<p>In this country this complex phosphate of -aluminum and copper is found in streaks and -patches in volcanic rocks, but in Persia comes -from metamorphic rocks. To the Persians it was -a magical stone, protecting the wearer from injuries, -and among the Pueblo Indians it was -regarded as of religious value in warding off evil. -The best turquois comes from Persia, but it has -been found at several points in the United States, -as in Los Cerrillos and Burro Mts., N. M., in -Mohave Co., Ariz., San Bernardino Co., Cal., -in Nevada and Colorado.</p> -<div class="pb" id="Page_162">162</div> -<h3 class="center"><span class="sc">Fluorine</span></h3> -<p>At ordinary temperatures the element fluorine -is a colorless gas, which was not obtained pure -until 1888, because it could not be contained in -vessels of glass, gold, platinum, etc. At that -time it was made and kept in a vessel composed -of an alloy of platinum and iridium. Its most -important compound is hydrofluoric acid, a fuming -liquid, which is mostly used to etch or dissolve -glass. It occurs in several minerals, like -tourmaline, turquois, etc., but the only one used -to obtain the hydrofluoric acid is fluorite.</p> -<h3><a id="species_Fluorite">Fluorite</a> -<br />CaF₂ -<br /><a href="#Plate_50">Pl. 50</a> -<br /><i>Fluor spar</i></h3> -<p>Occurs in crystals and cleavable -masses; hardness, 4; specific gravity, -3.2; colorless or some shade of violet, -green, yellow, or rose; luster vitreous; transparent -on thin edges.</p> -<p>Fluorite usually occurs in beautiful cubic -crystals, often with the edges and corners beveled -by smaller faces, and occasionally in twins, -which seem to have grown through each other. -There is perfect cleavage parallel to each of the -octahedral faces, which often, as in the illustration -on <a href="#Plate_50">Plate 50</a>, show as cracks cutting off the -corners.</p> -<p>Since fluorite loses weight and color on heating, -it is concluded that the colors are due to the -presence of hydrocarbon compounds. The red -and the green fluorite when heated to above -212° F. become phosphorescent, as may be seen -if they are thus heated and exposed to the light, -then taken into the dark.</p> -<p>Fluorite is quite commonly the gangue mineral -<span class="pb" id="Page_163">163</span> -associated with metallic ores, and is also likely -to occur with topaz, apatite, etc. It is generally -in such places that it seems to have been deposited -from hot vapors, rising from igneous -magmas.</p> -<p>It is the only mineral at all common from -which fluorine can be obtained, and is used for -making hydrofluoric acid, and other chemical -compounds of this element. It is, however, of -much greater importance as a flux in reducing -iron, silver, lead and copper ores. In the industries -it finds a place, being used to make apochromatic -lenses, cheap jewelry, and for the -electrodes in flaming arc lamps.</p> -<p>Fluorite is widely distributed, some of the -better known localities being Trumbull and Plymouth, -Conn., Rossie and Muscalonge Lake, -N. Y., Gallatin Co., Ill., Thunder Bay, Lake -Superior, Missouri, etc.</p> -<h3><a id="species_Halite">Halite</a> -<br />NaCl -<br /><a href="#Plate_50">Pl. 50</a> -<br /><i>Salt</i></h3> -<p>Occurs in crystals, and in cleavable -and granular masses; hardness, -2.5; specific gravity, 2.1; colorless to -white; luster vitreous; transparent on thin edges.</p> -<p>Halite is common salt, occurring in cubic -crystals, with perfect cubic cleavage. Its form, -hardness, taste, and solubility in water make it -easy to determine.</p> -<p>Halite is the most abundant salt in sea water, -making about 2.5% out of the total of 3.5% of -solids in solution. It is also a prominent, when -not the leading, salt in solution in the waters of -inland lakes, like Great Salt Lake, or the Dead -Sea, there being 20% of halite in the former and -<span class="pb" id="Page_164">164</span> -8% in the latter, though the total of solid in -solution in the water of the Dead Sea is greater -than that in Great Salt Lake.</p> -<p>The great salt deposits are mostly the result of -the evaporation of the water of arms or isolated -portions of former oceans; the salt, gypsum, etc., -left by the drying sea, having been buried beneath -later sediments. Other bodies of salt represent -the disappearance of ancient lakes. -There are also the curious “salt domes” of -Louisiana and Texas, which are immense, roughly -circular, subterranean masses of salt extending to -as yet unknown depths which are thought to have -been formed by masses of salt from some deep -source bed pushing their way upward through the -overlying formations by plastic flowage. As the -upthrust took place the sediments were arched -into domes. Some of these domes are today important -sources of rock salt.</p> -<p>There are extensive beds of salt under parts of -New York, Michigan, Ohio, Oklahoma, Kansas, -etc., which are mostly worked by drilling wells -into the salt layer, then introducing hot water to -dissolve the salt. The brine thus formed is -pumped to the surface, and the salt recovered by -evaporation in pans. During the process, skeleton -crystals of salt with concave faces may form, -but in Nature the crystals are uniformly solid -cubes.</p> -<h3><a id="species_Boracite">Boracite</a> -<br />Mg₇Cl₂B₁₆O₃₀</h3> -<p>Occurs in small crystals or granular -masses; hardness of crystals, 7; -of the masses, 4.5; specific gravity -3; colorless to white; luster vitreous; transparent -to translucent on thin edges.</p> -<div class="pb" id="Page_165">165</div> -<p>Small crystals, associated with salt and gypsum, -occur in the beds and incrustations, which -result from the drying up of alkaline lakes, -especially in Nevada and southern California. -The crystals are orthorhombic, but appear like -perfect cubes, with the edges beveled and part of -the corners cut. They are not easily dissolved in -water, but quickly go into solution in hydrochloric -acid.</p> -<h3><a id="species_Colemanite">Colemanite</a> -<br />Ca₂B₆O₁₁ + 5H₂O</h3> -<p>Occurs in crystals or compact -masses; hardness, 4.5; specific gravity, -2.4; colorless to white; luster -vitreous; translucent on thin edges.</p> -<p>The crystals when they occur, are monoclinic; -but usually colemanite is a bedded deposit, -which has resulted from the drying up of a saline -lake. It was first found in Death Valley, Cal., -in 1882, then near Daggett, Cal., and since then in -several similar locations in Nevada and Oregon. -The deposits are of all grades of purity, the colemanite -being mixed with varying quantities of -mud. Today this mineral is the chief source of -borax, which is used in medicines, cosmetics, -colored glazes, enamel, and as a preservative.</p> -<h3><a id="species_Borax">Borax</a> -<br />NaB₄O₇ + 10H₂O</h3> -<p>Occurs in crystals or in powdery -incrustations; hardness, 2; specific -gravity, 1.7; colorless to white; -luster vitreous; translucent on thin edges.</p> -<p>The crystals are tiny and monoclinic, this -mineral being usually obtained by the evaporation -of the saline waters of such lakes as Clear and -Borax Lakes in southern California, or from the -muds of salt marshes, like Searles Borax Marsh -<span class="pb" id="Page_166">166</span> -in California. Originally most of our borax -came from a large saline lake in Tibet, but now -most of it is obtained from colemanite. Borax is -soluble in water, giving it a sweetish taste.</p> -<h3><a id="species_Sulphur">Sulphur</a> -<br />S -<br /><a href="#Plate_51">Pl. 51</a></h3> -<p>Occurs in crystals, incrustations or -compact masses; hardness, 2; specific -gravity, 2; color yellow; streak -yellow; luster resinous; translucent on thin edges.</p> -<p>Aside from the numerous compounds, such as -the sulphides of the metals like pyrite, galena, -sphalerite, etc., and the sulphates, like gypsum, -barite, anglesite, etc., sulphur occurs in its elemental -form in Nature. In this case it may be in -crystals, which are orthorhombic and usually -occur as octahedrons, with the upper and lower -ends truncated, either by a basal plane, or by a -lower octahedron, or by both. Incrustations and -compact masses are, however, much the commoner -mode of occurrence. The incrustations -are found mostly about volcanic regions, where -the sulphur has risen from the molten lavas as a -sublimate, and on cooling has been deposited -in crevices or on the adjacent surfaces. Irregular -masses of sulphur are often found where sulphide -minerals, like pyrite or galena have been decomposed -in such a way as to leave the sulphur -behind. The extensive beds of sulphur are usually -associated with gypsum, and are thought to -be the result of water, containing bituminous -matter, so acting on gypsum as to remove the -calcium and oxygen as lime, and leave the -sulphur. Finally many waters carry sulphates -in solution, from which the sulphur may be -<span class="pb" id="Page_167">167</span> -precipitated by certain sulphur bacteria, making -thus incrustations on the bottom of ponds or lakes.</p> -<p>Sulphur is used for making matches, gunpowder, -fireworks, insecticides, in medicine, vulcanizing -rubber, etc. It is widely distributed, -however, most of the present world’s production -is from deposits associated with the “salt domes” -of Texas and Louisiana. A “caprock” of gypsum -and anhydrite overlies many of these which often -contains elemental sulphur. Wells are drilled into -this, and the sulphur is melted by the introduction -of hot steam. This melted sulphur is then pumped -to the surface and run into molds.</p> -<p>Some of the best known localities are Sulphurdale, -Utah, Cody and Thermopolis, Wyo., Santa -Barbara Co., Cal., Humboldt Co., Nev., and about -the hot springs of the Yellowstone Park.</p> -<h3><a id="species_Ice">Ice</a> -<br />H₂O -<br /><a href="#Plate_51">Pl. 51</a> -<br /><i>water</i></h3> -<p>Occurs solid as ice, snow and frost, -or liquid as water; hardness, 2; -specific gravity, .92; colorless to -white; luster adamantine; transparent on thin -edges.</p> -<p>Though we seldom think of ice, and its liquid -form, water, as a mineral, still it is one, and -perhaps the most important of all minerals, as -well as the most common. Ice melts at 32° F. -and vaporizes at 212° F., being then termed -steam. Because it is so common and liquid at -ordinary temperatures it acts as a solvent for a -host of other minerals, and is therefore the agent -by which they are transported from place to -place and redeposited in veins and beds.</p> -<div class="pb" id="Page_168">168</div> -<p>Not only does water act as a transportation -agent for minerals in solution, but is also the -agent of erosion and weathering. Water vaporizes -slowly when exposed to the air at all temperatures -above freezing, and so it is slowly rising -from the surface of the sea or lakes or moist -ground into the air, where it would accumulate -until the air was saturated, if the air would only -keep still and at a uniform temperature. The air -will hold a given amount of water vapor, which -is, for example, 17 grams per cubic meter when -the temperature is 68° F., but at 59° F. it will -hold only 12½ grams, or at 50° F. only 9 grams. -Thus the air is more or less completely saturated -at higher temperatures, and when the temperature -is lowered the air can not hold all it has -taken up, and it is precipitated in dew, rain or -snow, most often as rain. When the rain falls it -mechanically carries away, and more or less -slowly transports to other places particles of -rock, being thus the agent of erosion; and when it -is slowed down, as on entering the quiet water of -a lake or the sea, it drops the mechanically carried -sediment and makes sedimentary deposits.</p> -<p>Another very important and unique feature of -water is that on freezing it expands about ¹/₁₁th of -its former bulk, so that, as a result, ice floats, -and also wherever water in crevices is frozen, the -crevices are enlarged. In locations where this -freezing and melting take place repeatedly -throughout a year, there the breaking up of -rocks is rapid.</p> -<p>This is hardly the place to take up a complete -discussion of water, but its action as a solvent, -<span class="pb" id="Page_169">169</span> -mechanically, and in freezing, melting, and -vaporizing is the basis of a large part of the -study of geology.</p> -<p>When water crystallizes, as in forming ice, it is -in the hexagonal system. It tends to twinning -and a snow-flake is made up of a large number of -twinned crystals, each diverging from the other -at 60°. When ice is formed in the air or on the -surface of water it forms these complex and -beautiful multiple twins, of which but a couple -are suggested here. Beneath the surface the -hexagonal crystals grow downward into the -water, parallel to each other, making a fibrous -structure, which is very apparent when ice is -“rotten,” which is the time at which the surfaces -of the prisms are separating, because the molecules -leave the crystal in the reverse order to -which they united with it. Frost in marshy or -spongy ground will often show this fibrous growth -beautifully.</p> -<div class="pb" id="Page_170">170</div> -<h2 id="c5"><span class="h2line1">CHAPTER IV</span> -<br /><span class="h2line2">THE ROCKS</span></h2> -<p>Broadly speaking a rock is an essential part -of the crust of the earth, and includes loose material, -like sand, mud, or volcanic ashes, as well -as compact and solid masses, like sandstone and -granite. Rocks are aggregates of minerals, -either several minerals grouped together, as are -mica, quartz and feldspar to make granite, or -large quantities of a single mineral, like quartz -grains to make sandstone.</p> -<p>The rocks are most conveniently classified -according to their mode of origin, into three main -groups, igneous, sedimentary, and metamorphic. -The igneous rocks are those which have solidified -from a molten magma, like lavas, granites, etc. -The sedimentary rocks are those which represent -accumulations of fragments or grains, derived -from various sources, usually the weathering -of other rocks, and deposited by such agents -as water, wind and organisms. Metamorphic -rocks are those which were originally either igneous -or sedimentary, but have been altered -by the actions of heat, pressure and water, so -that the primary character has been changed, -often to such an extent as to be obscured.</p> -<p>Rocks once formed in any of the above ways -are being constantly altered in character by the -<span class="pb" id="Page_171">171</span> -various processes of nature. Those exposed on -the surface are weathered to pieces, and the fragments -are transported by wind or water to accumulate -elsewhere as sedimentary rocks. Those -buried deep beneath the surface are affected by -the high temperature and pressure of the depths -of the earth and thus metamorphosed. For instance -a granite exposed on the surface is slowly -weathered, some parts being carried away in -solution by the rain water, others less soluble -remaining as grains of quartz, mica or kaolin. -These are transported by water and sorted, the -finer kaolin being carried to still and deep water, -the quartz and mica accumulating in some lowland -as sand. This sand will in time be cemented -to a sandstone, later slowly buried beneath the -surface. If buried deep it will feel the effect -of the interior temperature, which increases as -one goes down at the rate of one degree F. for -every 50 feet. If this should be in a region where -folding and mountain-making takes place, the -material under the folds would be melted (because -of the relief from pressure which would -permit the high temperature to act freely) and -become igneous rock, either coming to the surface -as lava, or remaining below the surface and -making a granite or similar rock; while the -sedimentary material not melted but near -enough to the molten material to be affected, -would be metamorphosed, in this case to a quartzite. -Much of the interest and profit in studying -rocks, will come from the understanding which -they will give as to the history of that particular -part of the earth’s crust where they are found.</p> -<div class="pb" id="Page_172">172</div> -<h3 class="center"><span class="sc">Igneous Rocks</span></h3> -<p>Igneous rocks are those which have formed -from material that has been melted, which involves -temperatures around 1300° C.; or, if -there is water in the original material, temperatures -as low as 800° C. will suffice. Considering -the increase of temperature to be a degree for -every 50 feet downward, this involves the rocks -having been at depths of 5 to 10 miles below the -surface. While at such depths the temperature -must be high enough to melt rocks, the great -pressure of the overlying rocks seems to keep -them solid; for we know that the center of the -earth is solid, as is shown by a variety of observations, -such as the rate at which earthquake waves -are transmitted through the earth, the lack of -tidal effects, etc. However, there is every reason -to believe that if the pressure is removed from -the rocks which are five to ten miles below the -surface, there is heat enough at those depths to -melt them. When the crust of the earth is -folded, as when mountain ranges are formed, the -areas under the arches or upward folds are relieved -of pressure. Then those rocks, which are -under the arches and are relieved, become molten. -The molten magma may well up and fill the -space beneath the arch where it would cool again -very slowly; or, if there is fissuring during the -folding, some of the molten material may be -forced out through the fissures and pour out over -the surface as lava. Another area in which pressures -may be locally relieved is in the region of -faulting, where the crust of the earth is broken -<span class="pb" id="Page_173">173</span> -into blocks, between which there are readjustments, -some being tipped one way, some another, -some uplifted. Here again there would be areas -of relieved pressure and molten magmas would -form, some of them solidifying in place, others -rising to the surface.</p> -<p>The molten material is termed the <b>magma</b>, -and when it reaches the surface, great quantities -of water vapor and other gases escape: or these -gases may even escape from magmas which do -not reach the surface, rising through fissures. -As these hot vapors pass through the fissures, -they are cooled, and may deposit part or all of -their dissolved compounds in the fissure, making -veins. <b>Lava</b> is the magma minus the vapors. -Magmas vary greatly from place to place, indicating -that they are formed locally and do not -come from any general interior reservoir, as has -sometimes been suggested.</p> -<p>When the molten magmas escape to the surface, -they are termed <b>extrusive</b>, and as they -spread out in a layer this is termed a <b>sheet</b>. This -rise and overflow may be quiet, and from time -to time one outpouring may follow another making -sheet after sheet. Or after one outpouring, -the pressure below may cease for a time and -allow the lava to solidify and make a cap or -cover over the opening. Before more lava can -rise, this cover must be removed. This usually -happens in an explosive manner, the lava below, -with the increasing pressure exerted by its expanding -gases, finally exerting enough pressure, -so that the cover is broken, or shattered and -thrown in thousands of fragments into the air, -<span class="pb" id="Page_174">174</span> -as happened at Mt. Pelée on the Island of Martinique -in 1902. The fragments thrown into the -air are often termed volcanic ashes, though this -is not a good word for them, for they have not -been burned.</p> -<p>In case the molten magmas under the relieved -areas do not reach the surface they are termed -<b>intrusive</b>. Such magmas may remain in the -space under a mountain fold, or be forced in -fissures part way to the surface. When the magma -is forced into more or less vertical cracks and -there solidifies, and these are exposed by erosion, -they are termed <b>dikes</b>. Sometimes the magmas -have risen part way to the surface and then -pushed their way between two horizontal layers -of rock and there hardened, in which case they -are termed <b>sills</b>, when uncovered. The Palisades -along the Hudson River are the exposed edge of -a sill. Again the molten magmas may well up -and spread between two horizontal layers, but -come faster than they can spread horizontally, -and then the magma takes the form of a half -sphere, and the overlying layers of rock are -domed up over it. Such a mass is termed a -<b>laccolith</b>. In all these cases the mass of igneous -rock is only discovered when the overlying rocks -have been eroded off. The great mass of molten -magma under the arches of mountain ranges simply -cools slowly into a granitic type of rock. -These masses are exposed when the thousands of -feet of overlying rock are eroded off. When -these masses are exposed, if of but a few miles in -extent, they are called stocks, but, if of many -miles in length and breadth, they are <b>batholiths</b>, -<span class="pb" id="Page_175">175</span> -and are very characteristic of the heart of -mountain ranges.</p> -<p>In all the above cases the exterior of the molten -mass cools first, and forms a shell around the -rest. The shell determines the size of the mass. -As the cooling continues into the interior, it also -solidifies, and as all rocks shrink on cooling, -cracks develop, separating the mass into smaller -pieces. There is usually no regularity about -these cracks and the mass is divided into blocks -from six inches to three feet in diameter. However, -in some cases, especially in sills and laccoliths -where the cooling is slower, the shrinkage -may be marked by a regular system of cracks -which bound the rock into more or less regular -hexagonal columns. The Palisades and the -Devil’s Tower in Wyoming (See <a href="#Plate_52">Plate 52</a>) show -this structure. The Devil’s Tower is the remnant -of a laccolith, all except the central core of -which has been eroded away. All of the above -terms have nothing to do with composition, but -refer entirely to the manner of occurrence.</p> -<p>While the igneous rocks are classified according -to their composition, the rate at which they -cooled has much to do with their texture, and -certain names apply to the texture. For instance -when the molten lava cools very rapidly, there is -no time for the formation of crystals, and the -resulting rock is glassy or non-crystalline. If the -cooling is slow as in large bodies, crystals have -time to form and grow to considerable size as -in granites. Between these all grades may occur; -and one classification of igneous rocks expresses -their rate of cooling, in such terms as the following.</p> -<div class="pb" id="Page_176">176</div> -<p><b>Glassy</b>—lavas which have cooled so quickly -that they are without distinct crystallization, -such as obsidian, pitchstone, etc.</p> -<p><b>Dense or felsitic</b>—lavas which have cooled less -rapidly, so that crystals have formed, but in -which the crystals are too small to be identified -by the unaided eye, such as felsite or basalt.</p> -<p><b>Porphyritic</b>—magmas from which, in solidifying, -one mineral has crystallized out first and the -crystals have grown to considerable size, while -the rest have remained small.</p> -<p><b>Granitoid</b>—magmas which have solidified -slowly, so that all the minerals have crystallized -completely, and the component crystals are large -enough to be recognized readily, as in granite.</p> -<p><b>Fragmental</b>—a term applied to the fragments -which have resulted from explosive eruptions -of igneous rocks. These fragments may be loose -or consolidated. Volcanic ashes are typical.</p> -<p><b>Porous</b>—a term applied to the lava near the -upper surface, which is filled with gas cavities, -such as pumice.</p> -<p><b>Amygdoloidal</b>—is the term applied to porous -lavas, when the cavities have been filled by other -minerals, such as calcite or some of the zeolites.</p> -<p class="tb">In determining a rock, first decide whether it -is igneous, sedimentary or metamorphic. The -igneous character is recognized by its being either -glassy, or composed of masses of crystals irregularly -arranged, there being neither layering nor -bedding.</p> -<div class="pb" id="Page_177">177</div> -<h4>CLASSIFICATION OF IGNEOUS ROCKS</h4> -<table class="border" summary=""> -<tr class="th"><th><span class="sc">Texture</span> </th><th colspan="4">Excess of light colored minerals </th><th colspan="4">Excess of dark colored minerals</th></tr> -<tr><td class="l">Glassy </td><td colspan="4" class="l"><a href="#species_Obsidian">obsidian</a>, <a href="#species_Perlite">perlite</a>, <a href="#species_Scoria">pumice</a>, <a href="#species_Pitchstone">pitchstone</a> </td><td colspan="4" class="l"><a href="#species_Scoria">scorias</a>, <a href="#species_Trachite">trachylyte</a>, <a href="#species_Obsidian">basalt-obsidian</a></td></tr> -<tr class="th"><th> </th><th colspan="2">Feldspar orthoclase </th><th colspan="4">Feldspar Plagioclase </th><th colspan="2">No feldspar</th></tr> -<tr class="th"><th> </th><th colspan="2">Mica and/or hornblende and/or augite </th><th colspan="2">Mica and/or hornblende </th><th colspan="2">with pyroxene </th><th colspan="2">augite and/or hornblende and/or mica</th></tr> -<tr class="th"><th> </th><th>+quartz </th><th>-quartz </th><th>+quartz </th><th>-quartz </th><th>+olivine </th><th>-olivine </th><th>+olivine </th><th>-olivine</th></tr> -<tr><td class="l">Dense </td><td class="l"><a href="#species_Rhyolite">rhyolite</a> </td><td class="l"><a href="#species_Trachite">trachite</a> </td><td class="l"><a href="#species_Dacite">dacite</a> (felsite) </td><td class="l"><a href="#species_Andesite">andesite</a> (felsite) </td><td class="l"><a href="#species_Basalt">basalt</a> </td><td class="l"> </td><td class="l"> </td><td class="l"><a href="#species_Pyroxenite">augitite</a> or <a href="#species_Hornblende">hornblendite</a></td></tr> -<tr><td class="l">Porphyritic </td><td class="l"><a href="#species_Porphyry">rhyolite-porphyry</a> </td><td class="l"><a href="#species_Porphyry">trachite-porphyry</a> </td><td class="l"><a href="#species_Porphyry">dacite-porphyry</a> </td><td class="l"><a href="#species_Porphyry">andesite-porphyry</a> </td><td class="l"><a href="#species_Porphyry">basalt-porphyry</a> </td><td class="l"> </td><td class="l"> </td><td class="l"><a href="#species_Porphyry">augitite-porphyry</a></td></tr> -<tr><td class="l">Granitoid </td><td class="l"><a href="#species_Granite">granite</a> </td><td class="l"><a href="#species_Syenite">syenite</a> </td><td class="l"><a href="#species_QuartzDiorite">quartz-diorite</a> </td><td class="l"><a href="#species_Diorite">diorite</a> </td><td class="l"><a href="#species_OlivineGabbro">olivine-gabbro</a> </td><td class="l"><a href="#species_Gabbro">gabbro</a> </td><td class="l"><a href="#species_Peridotite">peridotite</a> </td><td class="l"><a href="#species_Pyroxenite">pyroxenite</a></td></tr> -<tr><td class="l">Fragmental </td><td class="l"><a href="#species_Rhyolite">rhyolite</a>, <a href="#species_Tuff">tuff</a> or <a href="#species_Breccia">breccia</a> </td><td class="l"><a href="#species_Trachite">trachite</a>, <a href="#species_Tuff">tuff</a> or <a href="#species_Breccia">breccia</a> </td><td class="l"><a href="#species_Dacite">Dacite</a>, <a href="#species_Tuff">tuff</a> or <a href="#species_Breccia">breccia</a> </td><td class="l">andesite <a href="#species_Tuff">tuff</a> or <a href="#species_Breccia">breccia</a> </td><td colspan="4" class="l">Basalt <a href="#species_Tuff">tuffs</a> and <a href="#species_Breccia">breccias</a></td></tr> -</table> -<div class="pb" id="Page_178">178</div> -<p>When it is located as igneous, turn to the key -on <a href="#Page_177">page 177</a> and decide as to which type of texture -is present. If glassy, the color, luster and -type of construction will place it. If the rock is -crystalline, first decide whether feldspar is present, -and if present, what type: then determine -the dark mineral, and lastly whether quartz or -olivine is present. In dense rocks the presence -of quartz may be determined by trying the hardness, -for none of the other constituents of igneous -rocks have so great hardness. For example, if it -is found that a rock is composed of orthoclase -hornblende and quartz, and the texture is granitoid, -it is granite: or if the rock is plagioclase feldspar -and pyroxene of any sort, it is gabbro, etc.</p> -<h3><a id="species_Granite">Granite</a> -<br /><a href="#Plate_53">Pl. 53</a></h3> -<p>The combination of orthoclase -feldspar (or microcline), quartz, and -either mica, hornblende or augite is -termed granite, if the texture is coarse enough so -the individual minerals can be recognized with -the unaided eye. The rock is light-colored because -the feldspar and quartz dominate. Accessory -minerals may be present such as apatite, -zircon, beryl or magnetite. Varieties of granite -are distinguished according to the dark mineral -present. When this is muscovite, it is a <i>muscovite-granite</i>; -when it is biotite, a <i>biotite-granite</i>; if -it is hornblende, a <i>hornblende-granite</i>; etc. The -size of crystals in granite varies widely. When -they are as small as ¹/₁₂ of an inch in diameter, it -is termed fine grained; from ¹/₁₂ to ¼ of an inch, -it is medium-grained; when larger, it is coarse-grained. -In some cases the crystals may be over -a foot in diameter which is known as <i>giant -granite</i>.</p> -<div class="pb" id="Page_179">179</div> -<p>Originally granite was a great mass of molten -magma, which has cooled very slowly, having -been intruded or thrust up in great stocks or -batholiths beneath overlying rocks, which acted -as a blanket to prevent rapid cooling. These -overlying rocks, in their turn, have been acted -upon by the heat and metamorphosed. Granite -is particularly likely to have been formed under -mountain folds; so that, after the mountains -have been more or less completely eroded away, -the great masses of granite have come to the surface -to mark the axes of the ranges; and even -after the mountains have been wholly worn away, -the granite remains to mark the sites on which -they stood.</p> -<p>In the granite mass itself, there are often veins -and dikes, which probably resulted from the -shrinkage of the cooling granite, and they are -filled with a different and usually coarser granite -known as <b>pegmatite</b>. This pegmatite formed -from the residual magmatic material, so that as -some of the elements had already crystallized -out, the granite in these dikes is of different composition. -The extreme coarseness of these pegmatites -seems to be due to the character of the -mineralizing agents left in the dikes. In some of -these pegmatites the feldspar and quartz are so -intergrown, that when broken along the cleavage -surface of the feldspar, the quartz appears -like cuneiform characters, and this variety has -been given the name <i>graphic granite</i> (See <a href="#Plate_53">Plate 53</a>).</p> -<p>When granite is exposed to weathering, the -feldspar is the first mineral to be decomposed, -<span class="pb" id="Page_180">180</span> -altering eventually into carbonates, quartz and -kaolin. The dark minerals are only slightly less -susceptible and they break down into carbonates, -iron oxides and kaolin. The original quartz -remains unchanged. Of these products the carbonates, -some of the iron oxide and a little of the -quartz are carried away in solution. The kaolin -and some of the iron oxide is in fine particles and -they are carried by the water until it comes to -the lakes or the sea. The quartz is left in coarser -grains, which are more slowly transported, and -deposited in coarser or finer sand and gravel beds.</p> -<p>Granites are widely used for building stone, -because they can be worked readily in all directions, -and have great strength and beauty. The -color depends largely on the color of the feldspar, -which may be white or pink, in which case the -granite will be gray to pink.</p> -<p>Granites occur throughout New England, the -Piedmont Plateau, the Lake Superior Region, -the Black Hills, Rocky Mountains, Sierra Nevada, -etc.</p> -<h3><a id="species_Syenite">Syenite</a> -<br /><a href="#Plate_54">Pl. 54</a></h3> -<p>The combination of orthoclase -and either mica, hornblende, or -augite is syenite, the texture being -coarse enough so that the individual minerals can -be distinguished by the unaided eye. It differs -from granite in the absence of quartz. Syenite -is a light-colored rock with the feldspar predominating. -Minerals like apatite, zircon, or magnetite -may occur in it, as accessory minerals. -The foregoing would be an ideal syenite, but -usually there is some plagioclase feldspar also -<span class="pb" id="Page_181">181</span> -present. If this occurs in such quantities as to -nearly equal the orthoclase feldspar, the rock is -termed a <i>monzonite</i>; if it predominates, the rock -becomes a diorite. The presence of quartz would -make this rock into a granite. Such a compound -rock has its type form, and when the proportions -of the component minerals are changed, it grades -into other types.</p> -<p>Like the granite, syenite is an intrusive rock, -which occurs in stocks and batholiths along the -axes of present or past mountain ranges. The -original magma welled up under the mountain -folds, where it cooled slowly, metamorphosing the -adjacent rocks. Like granite it has only been -exposed after a long period of erosion has removed -the overlying layers of rock.</p> -<p>Syenites are not as abundant as granites, but -they occur in the White Mountains, near Little -Rock, Ark., in Custer Co., Colo., etc.</p> -<h3><a id="species_QuartzDiorite">Quartz-Diorite</a></h3> -<p>The combination of plagioclase -feldspar, quartz and either mica or -hornblende makes quartz-diorite, -sometimes called <i>tonalite</i>. The above would -be the typical quartz-diorite, but there is usually -some orthoclase present, which if it equals -the plagioclase feldspar in amount makes this -into a monzonite; or if it dominates, it makes -the rock a granite. Quartz-diorite is darker -colored than the two preceding rocks, the dark -minerals being about as abundant as the light-colored -ones, such as feldspar and quartz. For -this reason the weight is also somewhat greater.</p> -<p>Like the others this is an intrusive rock, occurring -<span class="pb" id="Page_182">182</span> -in stocks and batholiths, and indicative -of great molten masses thrust up under mountain -folds, and only exposed after the overlying rocks -have been weathered away. It is by no means an -abundant type of rock, but occurs at Belchertown, -Mass., Peekskill, N. Y., in the Yellowstone -Park, etc.</p> -<h3><a id="species_Diorite">Diorite</a></h3> -<p>Plagioclase feldspar with hornblende -or mica, or with both, is -known as diorite. It is distinguished from -quartz-diorite by the absence of quartz. There is -generally some augite in it, but if this should be -equal to, or exceed the hornblende, the rock is -then a gabbro. There may also be a small -amount of orthoclase present, without taking this -rock out of the diorite class, but if the orthoclase -feldspar becomes dominant, then the rock is a -syenite. Thus there is gradation into other -groups in all directions. Apatite, magnetite, -zircon, and titanite often occur in small quantities -as accessory minerals. Generally the hornblende -is in excess of the feldspar, so that the -rock is a dark-colored one.</p> -<p>Diorites occur in much the same manner as -granites, being in stocks, batholiths or dikes, -and are often associated with granites and gabbros. -They are great intruded masses, associated -with mountain making, and like the preceding -rocks, cooled far below the surface, and have -been exposed only after great thicknesses of -overlying rocks have been weathered away.</p> -<p>Peekskill, N. Y., the Sudbury nickel district -in Canada, Mt. Davidson above the Comstock -<span class="pb" id="Page_183">183</span> -Lode in Nevada, etc., are typical localities for -finding diorite.</p> -<h3><a id="species_OlivineGabbro">Olivine-Gabbro</a></h3> -<p>The combination of plagioclase -feldspar with augite (or any of the -pyroxenes) and olivine makes olivine-gabbro. -The feldspar is usually one of those -with considerable calcium in it, like labradorite; -and as the dark minerals predominate, the rock -is dark-colored. It is an intrusive rock, usually -in dikes or stocks, where it solidified far below -the surface, and was only exposed after the overlying -rocks were weathered off. It is by no -means an abundant type of rock, but is found in -the Lake Superior Region, and near Birch Lake, -Minn.</p> -<h3><a id="species_Gabbro">Gabbro</a> -<br /><a href="#Plate_54">Pl. 54</a></h3> -<p>Plagioclase feldspar with any one -of the pyroxenes, most commonly -augite, is gabbro. There is a wide -range in the relative proportions of the two minerals -making gabbro. At one extreme are rocks -made entirely, or almost entirely, of plagioclase -feldspar, which are known as <b>anorthosites</b>, and -occur in parts of the higher mountains of the -Adirondacks like Mt. Marcy, in several places in -eastern Canada, etc. Then there are the typical -gabbros where the feldspar and augite are more or -less equally represented. At the other extreme -come those gabbros in which the pyroxene predominates, -in the most marked cases the feldspar -being entirely lacking, and the rock being termed -a pyroxenite. When the pyroxene of a gabbro is -either enstatite or hyposthene (usually the latter) -<span class="pb" id="Page_184">184</span> -the gabbro is often called <b>norite</b>. Magnetite, -biotite, and hornblende may occur in small -quantities as accessory minerals.</p> -<p>Gabbro is a common intrusive rock, occurring -in stocks, batholiths, and dikes, and often varies -considerably in different parts of the mass. Like -granite the mass solidified far below the surface, -under some mountain fold, and has only been -exposed as the result of weathering away the -layers of overlying rock. Gabbros appear much -like diorites, but are distinguished by the fact -that the dark mineral is one of the pyroxenes, -instead of an amphibole or a mica. They are -widely distributed, being found in the White -Mountains, near Peekskill, N. Y., Baltimore, -Md., about Lake Superior, in Wyoming, the -Rocky Mts., etc.</p> -<h3><a id="species_Peridotite">Peridotite</a></h3> -<p>A rock made up of olivine and -augite (or any of the pyroxenes) is -peridotite. As it contains no feldspar, and both -augite and olivine are dark-green to black in -color, these rocks are always dark green to black -in color and of considerable weight. They are -usually rather coarsely crystalline. Peridotite is -usually associated with gabbro, making dikes -which lead from the main gabbro mass. Less -frequently it occurs independently, making up -an intrusive mass. Hornblende and mica may be -present in small quantities, as accessory minerals.</p> -<p>In general these are rather rare rocks, making -dikes connected with stocks or batholiths of -gabbro. Peridotite is found near Baltimore, Md., -in Custer Co., Colo., in Kentucky, etc.</p> -<div class="pb" id="Page_185">185</div> -<h3><a id="species_Pyroxenite">Pyroxenite</a></h3> -<p>This represents the extreme among -coarsely crystalline igneous rocks, a -whole mass made up of one mineral, and that -some one of the pyroxene group. If the mineral -can be exactly determined, the rock may be still -more definitely named. For instance if it is all -augite, then the rock would be called augitite. -Like the preceding rocks, pyroxenite is an intrusive -rock, usually found in dikes, which are -connected with gabbro, and it represents the segregation -of one mineral out of the gabbro, and -its solidification at one point. Hornblende, -magnetite and pyrrhotite may be present as -accessory minerals. This is not a common -rock, but it illustrates the fact that all possible -combinations do occur, if the circumstances -have warranted it. It is found -near Baltimore, Md., Webster, N. C., and in -Montana.</p> -<h3><a id="species_Rhyolite">Rhyolite</a></h3> -<p>This is a combination of orthoclase -feldspar, quartz, and either hornblende, -mica or augite in which the crystals are -of such small size that they can not be identified -with the naked eye. In composition it corresponds -to granite, but it is much finer in texture. -It differs from trachite by having quartz while -the latter has none. This can usually be determined -by trying the hardness as none of the other -minerals are as hard as 7. It is much harder to -distinguish it from dacite which differs only in -having plagioclase feldspar in place of the orthoclase, -and only the microscope will enable one to -make this distinction. Where the distinction -<span class="pb" id="Page_186">186</span> -cannot be made these light-colored lavas are -often called <b>felsite</b>.</p> -<p>Rhyolite is usually an extrusive lava, occurring -in sheets, but sometimes it is intrusive, occurring -in sills, dikes, and laccoliths. In all these cases -the lava has solidified so rapidly, that the crystals -are tiny, and only the general effect of a -crystalline structure is distinguishable. Rhyolites -may occur with porphyritic structure, in -which case the presence of the larger feldspar -crystals will help to distinguish whether they -are orthoclase or not, making the determination -easier. The color of rhyolites is green, red or -gray, always a decided light shade.</p> -<p>Rhyolites are abundant in the western states, -as in the Black Hills, the Yellowstone Park, -Colorado, Nevada, California, etc.</p> -<h3><a id="species_Trachite">Trachite</a></h3> -<p>The combination of orthoclase -feldspar with mica, hornblende or -augite is termed trachite, if the texture is dense. -It is usually an extrusive lava of light color -(green, red or gray), and corresponds in composition -to syenite. It can be distinguished from -rhyolite by having no quartz, and so nothing to -show a hardness above 5.5; but it is difficult to -distinguish it from andesite, which differs only -in having plagioclase feldspar in place of orthoclase. -It sometimes occurs with a porphyritic -structure, in which case the feldspar crystals are -usually large enough to be distinguished.</p> -<p>Trachites are not abundant in America, but -some are found in the Black Hills of South Dakota, -in Custer Co., Colo., and in Montana.</p> -<div class="pb" id="Page_187">187</div> -<h3><a id="species_Dacite">Dacite</a></h3> -<p>The union of plagioclase feldspar, -quartz, and either hornblende or -mica is termed dacite, if the texture is dense. -It is an extrusive lava, occurring mostly in sheets -and dikes. It corresponds in composition to -quartz-diorite. As the texture is dense it is -difficult to distinguish dacite from rhyolite, for -both have quartz and differ only in the character -of the feldspar, so it is quite common to use the -term felsite which does not distinguish between -the two, and only states that the rock is dense, -light-colored and extrusive. When, as often -occurs, the texture is porphyritic, and the feldspars -are the large crystals, then exact determination -is fairly easy.</p> -<p>Dacites are rather common, occurring on McClelland -Peak, Nev., in the Eureka district, -Nev., on Lassen’s Peak, Calif., Sepulchre Mt. in -the Yellowstone Park, etc.</p> -<h3><a id="species_Andesite">Andesite</a></h3> -<p>The union of plagioclase feldspar -with mica, hornblende or augite, -makes andesite if the texture is dense. The lack -of quartz, and so no mineral which has a hardness -of over 5.5, makes it possible to distinguish -andesite from dacite or rhyolite, but it is hard to -distinguish this rock from trachite, which differs -only on having orthoclase feldspar in place of -plagioclase. When the texture is porphyritic and -the feldspars are the large crystals, then it is easy -to make the distinction. Andesite gets its name -from being the characteristic lava of the Andes -Mountains, and is the commonest of all the extruded, -light-colored lavas, being the lava of -<span class="pb" id="Page_188">188</span> -hundreds of flows throughout the western United -States.</p> -<p>The union of plagioclase feldspar and biotite -is the commonest type. Plagioclase with hornblende -or augite is less common, and, when they -do occur, they are usually distinguished as -<i>hornblende-andesite</i> or <i>augite-andesite</i>. Magnetite, -apatite and zircon may be present as accessory -minerals.</p> -<p>The lavas of Mt. Hood, Shasta, Rainier and -others of the volcanic peaks of the Cascade -Range, those at Eureka and Comstock in Nevada, -in the Yellowstone National Park, and -the porphyries of many peaks in Colorado, like -the Henry Mts., etc., which are exposed laccolithic -intrusions, are all andesites, as are many -more.</p> -<h3><a id="species_Basalt">Basalt</a></h3> -<p>The combination of plagioclase -feldspar with olivine and augite (or -any other pyroxene) makes a heavy, dark-colored, -black to dark-brown rock which, if its -texture is dense or porphyritic, is termed basalt. -This usually has more or less magnetite in it as an -accessory mineral, indeed the magnetite may be -so abundant as to be a component part of the -rock. This magnetite makes trouble for anyone -trying to use a compass on or about basalt rocks. -These are extrusive or intrusive rocks and correspond -in composition to gabbro.</p> -<p>Basalts are among the commonest of igneous -rocks, and are popularly designated “<i>trap</i>,” much -used as a road ballast on account of its toughness, -which is largely due to its dense texture. The -<span class="pb" id="Page_189">189</span> -coast of New England is seamed with dikes of -basalt, and through the Adirondack and White -Mountains there are a host of these dikes. The -crests of such mountains, as the Holyoke Range, -the Tom Range, the Talcott Mts., East and West -Rocks at New Haven, etc., are all basalt sheets. -The Palisades, First Wachung and Second Wachung -Mountains of New Jersey are sills of -basalt. The Lake Superior region is crisscrossed -with basalt dikes. That greatest of all lava fields -the Columbia Plateau, covering over 200,000 -square miles on the Snake and Columbia Rivers -in Oregon, Washington and Idaho, is all basalt. -So it goes all down through Nevada, New Mexico -and California.</p> -<h3><a id="species_Porphyry">Porphyry</a> -<br /><a href="#Plate_55">Pl. 55</a></h3> -<p>This is a term which properly refers -to texture alone, indicating a -lava, which has cooled in such a -manner that one mineral has crystallized out of -the magma first and developed to a larger size, -while the mass of the material formed tiny crystals -in which the larger ones are embedded. The -large crystals are technically known as <i>phenocrysts</i>. -The surrounding mass of tiny crystals -is termed the <i>matrix</i>. This porphyritic structure -is especially characteristic of lavas which -have been extruded in large masses, and of -intruded lavas in such places as sills and -laccoliths.</p> -<p>The term porphyry today has the above precise -meaning. It is a much abused word, and -has had all sorts of meanings. In the past it was -first used to refer to lavas in general, then it came -<span class="pb" id="Page_190">190</span> -to be applied to lavas which had been erupted -before Tertiary times, that is to all ancient lava -sheets. This idea soon proved incorrect, lavas -being of the same composition whether ancient -or recent. In the West the word is often colloquially -used today to designate almost every -kind of igneous rock occurring in sheets or dikes, -if in any way connected with ore deposits.</p> -<p>When the composition of a rock with porphyritic -textures can be determined, the name -due to the composition is coupled with that due -to texture, making such terms as <i>trachite-porphyry</i>, -<i>basalt-porphyry</i>, etc.</p> -<h3><a id="species_Tuff">Tuff</a></h3> -<p>Tuff, a term not to be confused -with tufa on <a href="#Page_215">page 215</a>, is the name -used to designate the finer fragmental ejecta of -volcanic eruptions, which are also often referred -to as “volcanic ash,” but the word, ash, conveys -the false impression that the rock is a remnant -of something burned, and is therefore not a good -term. When first ejected, tuff is loose material, -but it is usually soon cemented to make a more -or less firm mass of rock, for which the term, tuff, -is still retained. In some cases, while still loose, -it is carried by streams to a distance and deposited -in more or less sorted and layered beds: -and the finer tuff is often carried by the winds -and laid down, at a considerable distance from -its source, in so called “ash beds.” In both these -cases, sedimentary characteristics have been -added to the tuff, and layering which is characteristic -of sedimentary deposits, is present. -These transported tuff beds are really sedimentary, -<span class="pb" id="Page_191">191</span> -but as there is little change in the material, -they are referred to here and not again. These -tuff beds are not at all uncommon in the sedimentary -deposits of Tertiary age in the Rocky -Mountain region. The coarser material of -volcanic eruptions usually goes under the head -of breccia.</p> -<h3><a id="species_Breccia">Breccia</a></h3> -<p>This term is used to describe the -coarse fragmental ejecta of volcanic -eruptions. It is also used, in the section under -sedimentary rocks, in a broad sense to include -all angular unworn fragmental material, whether -of igneous or sedimentary origin. For this -reason, when dealing with igneous rocks, it is -usual to designate the fragments according to -their composition, making such terms as <i>trachite-breccia</i>, -<i>rhyolite-breccia</i>, etc.</p> -<p>While still loose (and also even when cemented -into beds of rock), it is customary to designate -the smaller fragments, from the size of a grain of -wheat up to an inch or two in diameter, as -<i>lapilli</i>; the larger fragments, from two inches -up to a foot or so in diameter, as <i>bombs</i>; and the -largest masses, often tons in weight, as <i>volcanic -blocks</i>.</p> -<h3><a id="species_Obsidian">Obsidian</a> -<br /><a href="#Plate_55">Pl. 55</a></h3> -<p>Lavas, which have cooled so -quickly that crystals have not had -time to form, have a glassy appearance, -and are termed obsidian. If the color -is dark, due to the presence of large amounts of -those elements which make dark minerals, this -lava is termed <i>basalt-obsidian</i>. Obsidian is -<span class="pb" id="Page_192">192</span> -characterized by its glassy texture, a hardness -around 6, and by breaking with a conchoidal -fracture, so called because the surface is marked -by a series of concentric ridges, something like -the lines of growth on a shell. Obsidians vary -greatly in color, but are usually red or green to -black, and translucent on thin edges. While -glassy, all the obsidians contain embryonic -crystals, which appear like dust particles floating -in the glassy matrix, or there may even be a few -larger crystals present, which are often arranged -in flow lines. Most all large masses of obsidian -have streaks or layers of stony material in them -where crystallization has set in, in a limited -way.</p> -<p>Near the upper surface, obsidians usually have -gas cavities scattered through them, and these -may be small and few, or large and numerous. -Indeed the cavities may be so numerous as to -dominate and give the rock a frothy appearance. -In this case, if the cavities are small and more or -less uniform, the rock is called <i>pumice</i>; if they -are larger it is <i>scoria</i>. If, as often happens -when the lava is ancient and has been buried -beneath other rocks, the cavities have been -filled with some secondary mineral, then the -lava is called an <i>amygdoloid</i>.</p> -<p>Obsidian is found in many localities, especially -where there are recent volcanoes, the most -famous places being the obsidian cliffs in the -Yellowstone Park, those near Mono Lake in -California, and many other localities in the -Rocky Mountains, the Sierra Nevadas, and the -Cascade Mountains.</p> -<div class="pb" id="Page_193">193</div> -<h3><a id="species_Pitchstone">Pitchstone</a></h3> -<p>This is very like obsidian in -appearance, but differs in that the -glassy material contains from five to ten per cent -of water in its composition, the most obvious -effect of which is to make the luster resinous, -instead of vitreous, as is characteristic of obsidian. -The colors are commonly red, green or -brown. Pitchstone is associated with recent -volcanoes, and some fine specimens have come -from Silver Cliffs, Colo., and various parts of -New Mexico and Nevada.</p> -<h3><a id="species_Perlite">Perlite</a> -<br /><i>pearlstone</i></h3> -<p>Perlite is a glassy lava, containing -two to four per cent of water, which, -on cooling, has cracked into numerous -rounded masses, with a concentric structure, -reminding one of the layers of an onion.</p> -<h3><a id="species_Scoria">Scoria</a></h3> -<p>While lava is cooling, there is a -constant escape of gases, mostly -steam, and as these rise through the molten -mass they make cavities, near the upper surface, -that portion on top often becoming frothy. If -this solidifies quickly so that the gas cavities are -preserved it is scoria. When the gas cavities are -small and uniformly distributed, the rock is -called pumice, and often used as a scouring -agent. When the cavities are large and irregular -the term scoria is generally used. Molten lavas -may form various structures, according to the -conditions under which they cool, dripping -through cracks or from the roof of caves, which -often form where the molten lava escapes from a -hardened shell, and making stalactites, stalagmites, -<span class="pb" id="Page_194">194</span> -etc. The very thin lava of the Hawaiian -volcanoes may even be blown by the wind into -fine threads, known as “Pele’s hair.”</p> -<p>The presence of the gas cavities is so characteristic -of the upper surface of lavas which have -been extruded; that, where one is dealing with -older lavas, now buried beneath other rocks, this -fact helps to determine whether the mass is a -sheet, rather than a sill; for, in the case of the -sill, the lava was forced between layers of -sedimentary rocks, and the burden of the overlying -rocks did not permit the escape of steam -and therefore the upper surface of sills does not -have the scoriaceous structure.</p> -<h3><a id="species_Amygdoloid">Amygdoloid</a> -<br /><a href="#Plate_56">Pl. 56</a></h3> -<p>When the upper surface of a lava -is filled with steam holes, and this -lava has been buried beneath other -rocks, the seeping waters slowly bring such -minerals as quartz, calcite and zeolites and fill -the cavities. Such a rock is known as an -amygdoloid. It is often confused with porphyry; -but, if examined closely, it will be seen -that the outlines of the gas cavities are rounded, -while the outlines of a crystal, like a phenocryst, -are always angular. This will be clear if -the amygdoloid on <a href="#Plate_56">Plate 56</a> is compared with -the porphyry on <a href="#Plate_55">Plate 55</a>.</p> -<h3 class="center"><span class="sc">The Sedimentary Rocks</span></h3> -<p>To this class belong all those rocks which have -been laid down by water or wind, or are the -results of organic depositions. They include -<span class="pb" id="Page_195">195</span> -loose material like sand or day, and also the -same materials, when cemented into more or -less solid rocks, like sandstone or shale. So long -as the material has not been altered from what -it was when laid down, the rock is termed -sedimentary.</p> -<p>In general the material of which these rocks -are composed comes from the weathering and -disintegration of other rocks. This does not -apply to the organic deposits, for each type of -which there is a peculiar mode of formation. -To illustrate the typical formation of sedimentary -rocks, we may look at the fate of a granite -when exposed. At once the surface is attacked -by changes of temperature, frost and rain. The -various minerals of the granite expand and contract -with every change of temperature, but each -component mineral has a different coefficient of -expansion under heat, so that minute cracks are -quickly formed between the minerals. Water -gets into these cracks and begins to dissolve the -minerals. Feldspar is the most easily attacked, -part of it being dissolved and carried away, a -small part changing to quartz, and by far the -largest part changing to kaolin. The dark -mineral is also attacked and partly dissolved, -and partly changed to kaolin and iron oxides. -The quartz resists solution almost completely. -Of these products the kaolin and iron oxides -are carried far away and deposited in still water. -The quartz and perhaps some of the dark mineral -are heavier and carried more slowly, being -deposited as sand. This happens to granite -everywhere, but in the regions where there is -<span class="pb" id="Page_196">196</span> -frost the action is greatly hastened; for water gets -into the cracks and expands every time it freezes -and thus widens the cracks rapidly, which greatly -facilitates the entrance and movement of water -in the rock. In a similar way any original rock -will be disintegrated, and the residue, after the -soluble part has been carried away, becomes sand -or clay or mud.</p> -<p>Particles of quartz, kaolin, and lime, separately, -or mixed, loose or more or less cemented, -with accompanying impurities, make up the -great bulk of the sedimentary rocks. They -are usually arranged in layers, of varying thickness, -as they were laid down by water or the -wind. In the same way layered accumulations -which are either products of plants or animals, -or parts of the plants or animals, are considered -sedimentary, as for instance, coal, chalk, petroleum, -etc.</p> -<h3 class="center"><span class="sc">A Classification of Sedimentary Rocks</span></h3> -<table class="center" summary=""> -<tr><td colspan="2" class="l">Inorganic origin:</td></tr> -<tr><td class="r">1. </td><td class="l">Coarse fragmentary material resulting from weathering </td><td class="l">talus</td></tr> -<tr><td class="r">2. </td><td class="l">The same fragmentary material cemented </td><td class="l">breccia</td></tr> -<tr><td class="r">3. </td><td class="l">Unsorted material resulting from rock weathering </td><td class="l">soil</td></tr> -<tr><td class="r">4. </td><td class="l">Coarse fragments rounded by the action of water and wind </td><td class="l">gravel</td></tr> -<tr><td class="r">5. </td><td class="l">The same material cemented </td><td class="l">conglomerate</td></tr> -<tr><td class="r">6. </td><td class="l">Finer material deposited by water or wind </td><td class="l">sand</td></tr> -<tr><td class="r">7. </td><td class="l">The same material cemented </td><td class="l">sandstone</td></tr> -<tr><td class="r">8. </td><td class="l">The finest material, mostly kaolin, deposited by water </td><td class="l">clay</td></tr> -<tr><td class="r">9. </td><td class="l">The finest material, deposited by wind </td><td class="l">loess</td></tr> -<tr><td class="r">10. </td><td class="l">The same material cemented </td><td class="l">shale</td></tr> -<tr><td class="r">11. </td><td class="l">Fine particles of lime, pure or impure </td><td class="l">marl</td></tr> -<tr><td class="r">12. </td><td class="l">The same material cemented </td><td class="l">limestone</td></tr> -<tr><td class="r">13. </td><td class="l">Unassorted material left by the glacial ice </td><td class="l">till</td></tr> -<tr><td class="r">14. </td><td class="l">The same material cemented </td><td class="l">tillite</td></tr> -<tr><td colspan="2" class="l">Organic Origin:</td></tr> -<tr><td class="r">15. </td><td class="l">Limes made from shells, etc. </td><td class="l">coquina, chalk, coral rock, etc.</td></tr> -<tr><td class="r">16. </td><td class="l">Silica from the shells of plants, etc. </td><td class="l">diatomaceous earth, etc.</td></tr> -<tr><td class="r">17. </td><td class="l">Carbon from plants </td><td class="l">peat, lignite, coal, etc.</td></tr> -<tr><td class="r">18. </td><td class="l">Hydrocarbons from animals </td><td class="l">petroleum, asphalt, amber, etc.</td></tr> -<tr><td class="r">19. </td><td class="l">Phosphates from animals </td><td class="l">guano, phosphate rock, etc.</td></tr> -</table> -<div class="pb" id="Page_197">197</div> -<h3><a id="species_Talus">Talus</a></h3> -<p>Where weathering is very active, -especially on or below steep mountain -slopes, a mass of loose, angular fragments -accumulates. This material is termed talus, a -term which refers only to the physical character -of the material, and not at all to its composition. -If weathering continues these fragments will be -<span class="pb" id="Page_198">198</span> -further broken up into one of the finer grained -rocks, which the water can carry away and deposit -elsewhere. There is little or no layering in -talus. If the talus is not carried away but is -cemented where it was formed, the resulting -mass is termed breccia, but this is not very -commonly the case.</p> -<h3><a id="species_Breccia_rock">Breccia</a> -<br /><a href="#Plate_58">Pl. 58</a></h3> -<p>The term breccia is used to cover -all those rocks which are composed -of angular fragments, of any composition, -and above sand in size, when they are -cemented into a solid mass, by any sort of -cementing agent. Here the term is used in its -broad sense, as compared with the way it was -used under igneous rocks.</p> -<p>Breccias may result from the cementing of -talus, but more often the breaking up of the -material into angular fragments was due to -other causes, such as crushing along a fault -plane, or in the movements involved in mountain -making. In such cases the breccia is of limited -extent, but may occur repeatedly in the same -neighborhood. Limestone, which has been -crushed and then recemented, often makes a -rock which takes a good polish and is used in -several localities as an ornamental stone in place -of marble, in fact often goes in trade circles -under the name of “marble.” The breccia -figured on <a href="#Plate_58">Plate 58</a> is such a limestone.</p> -<h3><a id="species_Soil">Soil</a></h3> -<p>Over most of the earth’s surface -there is a covering of rock waste, -the product of weathering, some of which is -<span class="pb" id="Page_199">199</span> -unassorted, and some of it sorted by water or -wind. This is all termed soil. It is an ever-moving -cover resulting from the decomposition -of the underlying rocks, to which have been -added in places layers of rock waste brought -from afar by the streams. Some soils are rock -waste which had been carried clear to the ocean -and deposited on the floor of the sea, and is now -above sea level, because the floor of the sea -has been elevated. Inasmuch as the underlying -rocks vary in composition, and as there are -areas of transported material, it is clear that -the composition of soils must vary from place to -place, both as to composition and texture.</p> -<p>Soils range from the finest, composed mostly -of clay, to coarse ones, composed of sand, gravel -or even boulders. Clay, the finest grained soil, -is composed of particles only about ¹/₁₀₀₀th of a -millimeter in diameter, of which it would take -720,000 billion particles to make a gram’s weight. -Ordinary soils however have about 2 to 5 million -particles to the gram.</p> -<p>The average specific gravity of soil with the -usual amount of humus in it is from 2.55 to 2.75. -In this case however the specific gravity is of -less importance than is the volume weight. A -cubic foot of water weighs 62½ pounds, that of -soil from 75 to 80 pounds, the extremes being -30 lb. for peaty soil and 110 lb. for calcareous -sand. The terms “heavy” and “light,” used -in agriculture do not refer to the volume weight, -for clay which is actually relatively light (70-75 -lb. per cubic foot) is classed as a “heavy” soil; -while sand, of much greater actual weight, is -<span class="pb" id="Page_200">200</span> -classed as a “light” soil. These terms as used -in agriculture refer to the ease with which the -soils are worked, and to their penetrability by -plant roots.</p> -<p>Soil is usually divided into an upper darker-colored -layer, termed loam, and into a lower, -lighter-colored layer, termed subsoil. The presence -of humus, resulting from the decomposition -of plant and animal remains is the factor which -darkens the color and distinguishes the loam; so -that loam is a complex of inorganic rock particles -plus more or less humus, colloid compounds, -bacteria, living plants and animals. The subsoil -is mainly rock particles. The distinctions -between these two layers break down in arid -soils, and often also in swampy regions.</p> -<p>It is this layer of soil on which the water of -every rain and flood works, picking part of it up -and carrying it along, step by step, to the sea. -Though the amount moved on any one day is -small, the sum of all the soil transported is -enormous, a large river carrying annual incredible -amounts. For instance the Mississippi -annually deposits in the Gulf of Mexico 476,900,000 -metric tons (2204 lb. to the metric ton), of -which about a third is in solution. At this rate -it takes about 7000 to 9000 years to remove a foot -from over the whole drainage basin. This is -considerably slower than is the case of some -other rivers. While on the one hand soil is -being continuously carried away from the surface, -on the other hand it is being constantly -renewed from below, by the weathering action of -water, air and temperature.</p> -<div class="pb" id="Page_201">201</div> -<h3><a id="species_Gravel">Gravel</a></h3> -<p>Gravel is a mass of loose fragments -of rock, which have been -rounded by water and deposited with little or no -sorting, so that larger and smaller pebbles and -sand all occur together. It is the deposit laid -down by comparatively fast water in inland lakes -or along the storm-beaten shores of the sea. -Where a swift stream enters quiet water, as -where it empties into a lake, there it quickly -drops its coarse material as gravel, usually thus -building a delta. Gravel also occurs in stream -beds, where for any reason the rate of flow is -checked. During the recent glacial period, the -ice sheet brought down great masses of unsorted -material, which was deposited as till, or in -moraines. Much of this was then picked up by -the running water and moved longer or shorter -distances, so that, all over the glaciated country -of the northern and eastern United States, there -are unusually large numbers of gravel deposits. -Gravels are all water laid, and usually show more -or less clearly the bedded or stratified structure.</p> -<p>The size of the component pebbles of gravel -ranges from great boulders to fine sand, and the -finer gravels grade into the coarser sands, the line -between gravel and sand being drawn at about -the size of a pea, the coarser being gravel, the -finer sand.</p> -<p>Gravel is widely used as ballast for railroads -and in making highways, because of its tendence -to pack well, while the hard pebbles resist wear. -It is also widely used in concrete work, bonding -in well with the cement, and making it go from -three to five times as far.</p> -<div class="pb" id="Page_202">202</div> -<h3><a id="species_Conglomerate">Conglomerate</a> -<br /><a href="#Plate_58">Pl. 58</a></h3> -<p>Conglomerates are composed of -rounded pebbles and sand of varying -sizes, cemented together into a -solid rock. The pebbles may run up to boulders -in size, but they have all been more or less -rounded by water, and transported some distance. -The pebbles may all be of the same -composition, or may represent a variety of rocks. -When the pebbles are all, or most all, of one sort, -the resulting conglomerate is termed a <i>quartz-conglomerate</i>, -a <i>limestone-conglomerate</i>, a <i>gneiss-conglomerate</i>, -etc. So too the cementing material -varies in kind, silica, calcite and iron oxide being -the commonest. The color will depend on both -the component pebbles and the cement, sometimes -one dominating, sometimes the other. -There are some of the quartz- and limestone-conglomerates -which can be cut and polished to -make very handsome stone.</p> -<p>Conglomerates represent consolidated gravels, -and always indicate an aqueous origin, quite -often the delta of an ancient stream, or the -invasion of the sea over the land; so they have -become of importance to geologists in interpreting -past events.</p> -<h3><a id="species_Sand">Sand</a></h3> -<p>Sand is a mass of small rock particles, -from the size of a pea down to -¹/₅₀₀ of an inch in diameter. The material may -be any sort of rock, or a mixture of two or more -kinds. Sand may be the result of the disintegration -of older rocks at the point where it -is now found, in which case the grains have the -shapes they had in the original rock; but more -<span class="pb" id="Page_203">203</span> -often the sand grains have been transported -greater or lesser distances, and in the process -have been more or less rounded.</p> -<p>Those sands, which lie where they were formed -are called <i>residual</i>, and such sand is usually composed -of a mixture of angular grains, some harder -and others softer, such as quartz, feldspar, mica -and hornblende, all mixed together. Where the -sand has been transported, only the more resistant -minerals have remained, such as quartz, -magnetite, cassiderite, etc.; with which there -are at times rarer minerals, such as gold, -platinum, garnets or topaz. Such sands are -known as <i>gold-bearing</i>, <i>topaz-bearing</i>, etc.</p> -<p>The sands from different localities differ -greatly. The streams gather the rock particles, -and sort them according to the size, which the -water flowing at any given rate can carry. -When the water is slowed down, it drops all the -particles above the size which the new rate of -speed can handle. The grains of sand from the -bed of a stream are usually more or less angular. -The further they are carried, the more they are -knocked together and rounded; so that after -being carried to the sea, and then thrown up on -the beaches, they have been well rounded, -especially the larger grains. As the air is less -viscid than the water, sand which is transported -by the wind, is even more rounded; so that desert -sands show the most complete rounding, indeed -are even polished; and this is true even of the -smaller grains. It is the wind-blown, or desert -sands, which flow so evenly in an hourglass. Between -the angular residual sands and the -<span class="pb" id="Page_204">204</span> -polished desert sands, there are of course all -grades. Glacial sands are angular or “sharp” -almost to the degree characteristic of residual -sands; and lake-shore sands are between river -sands and sea sands in the degree of rounding.</p> -<p>Sands made of particles of lime, <i>calcareous -sands</i>, are less resistant to wear than are those -of quartz. In regions where the water is “soft” -(free from lime), they do not last long, as they -are dissolved; but in a limestone region where -the water is “hard” (saturated with lime), the -grains are not so quickly dissolved and may -accumulate into beds of great thickness, as in -Florida. Along some shores of the ocean, there -occur “green sands,” which are ordinary quartz -sands mixed with the dark green mineral glauconite, -which is a potassium iron silicate, forming -on the ocean bottom as a result of the action of -decaying animal matter on iron-bearing clays -and potassium-bearing silicates, like feldspar. -This is particularly characteristic of some of the -sands along the coast of New Jersey.</p> -<p>In places, especially in the beds of rivers, there -occur “quicksands.” This is a deposit of fine -sand, mixed with a considerable amount of clay, -and saturated with water; so that it will not -support the weight of a man or an animal. -Much that goes under the name of quicksand is -a fluid mud, covered with a thin layer of sand.</p> -<p>Sand is used for a wide variety of commercial -purposes, and under these conditions gets various -trade names; for instance “glass sand” is a pure, -colorless to white, quartz sand, which is used as -one of the components in making glass. It must -<span class="pb" id="Page_205">205</span> -be free from impurities, as these color the glass, -and much of the sand used for this purpose is -quartz, crushed to a fine sand-like condition. -“Moulding sand” is a rather fine-grained quartz -sand, with a small but very definite admixture of -clay, and this is used to make the moulds for -castings in foundries. “Polishing sand” is one -composed of angular fragments of quartz, usually -from stream beds or glacial deposits, or even -crushed quartz, and is used for cutting and -polishing marble, for sandpaper, and for polishing -wood and softer stones. There are many -other special uses, like building, ballast, filters, -furnaces, etc., in which quartz sand is used, being -screened if necessary to get the right sizes.</p> -<h3><a id="species_Sandstone">Sandstone</a></h3> -<p>When sand of any sort is cemented -so as to make a solid rock, it is -termed sandstone, which varies widely according -to the size, color and composition of the -grains, and also with the sort and amount of -the cement. When the size of the grains is -larger than that of a pea, sandstone grades into -conglomerate; when smaller than ¹/₅₀₀th of an -inch, especially if mixed with clay, it grades into -shale. There are all grades of firmness, due to -the amount and kind of cement, ranging from -those which have little or no cement, but are -compact as a result of the pressure of the overlying -rocks, to those in which the cement has -filled all the pore spaces. In general there is -a considerable amount of space between the -grains of sand; so that a sandstone will absorb -large amounts of water, up to 25% of its bulk. -<span class="pb" id="Page_206">206</span> -In moist climates where it freezes, this makes -many sandstones unsuitable for use as building -stones, as they are likely to spale, or chip off, as -is seen in the “brown stone” so much used in -New York City.</p> -<p>Sandstones are usually bedded rocks and are -relatively easy to quarry, and most of them are -not so firmly cemented, but that they can be -readily worked or cut into shape by the stone -cutter; and so, certain sandstones are very -popular for building stone or for trimming on -buildings, where they are not too much exposed -to the weather.</p> -<p>Sandstone gets a variety of names according -to the cement.</p> -<p><b>Siliceous sandstone</b> is cemented with silica -and usually very hard.</p> -<p><b>Calcareous sandstone</b> is cemented with lime -and usually rather soft.</p> -<p><b>Ferruginous sandstone</b> is cemented with one -of the iron oxides.</p> -<p><b>Argillaceous sandstone</b> is held together with -clay impurities, and is usually both soft and of -undesirable color.</p> -<p>According to their composition there is also a -number of varieties.</p> -<p><b>Arkose</b> is a sandstone composed of quartz and -feldspar grains, usually derived from the disintegration -of granite and not transported far.</p> -<p><b>Graywacke</b> is a sandstone composed of quartz, -feldspar, and some other mineral, like hornblende-augite, -etc., also derived from the disintegration -of granites and not transported far.</p> -<p><b>Grit</b> is a term applied to a coarse sandstone, -<span class="pb" id="Page_207">207</span> -composed of angular quartz fragments, and used -to a considerable extent for millstones.</p> -<p><b>Flagstone</b> is a thin bedded sandstone, often -with mica, which splits easily and uniformly -along the bedding planes; so that it can be quarried -in large slabs. It was widely used for sidewalks -before the advent of concrete.</p> -<p><b>Freestone</b> is a thick-bedded sandstone, not -over hard, so called, because it can be worked -freely and equally well in all directions.</p> -<h3><a id="species_Clay">Clay</a></h3> -<p>Clay is a term used to describe a -mass of fine particles, the most -prominent property of which is plasticity when -wet. Clays range from masses of pure kaolin -to masses of kaolin and related minerals mixed -with as much as 60% of impurities, which may -be sand, lime, iron oxides, etc. The particles of a -fine clay range around ¹/₁₀₀₀ of a millimeter in diameter, -while the impurities may be, and usually -are, of larger size, up to the size of sand grains.</p> -<p>All clays are of secondary origin, the result of -weathering, especially of feldspars, though clays -may also result from the weathering of serpentines, -gabbros, etc. In some cases after the -weathering of feldspar or limestones, the clay -may remain just where it was formed, as a -residual deposit; but, being so fine-grained, it is -usually transported by rain water or by the wind -and deposited somewhere else as a sedimentary -bed. The quiet waters of a lake are favorable -places for such deposits, and many clay beds -represent former lake bottoms. Impure clays -are often laid down on the flood plains of sluggish -<span class="pb" id="Page_208">208</span> -streams. In fresh water the settling of the -clay is a very slow process, requiring days, or -when very fine, weeks, before the water wholly -clears. In salt water, however, the clay sort of -coagulates, the particles gathering together in -tiny balls, which settle rapidly, so that the water -is soon clear.</p> -<p>According to their mode of origin clays are -classified as residual, sedimentary, marine, -swamp, lake, flood-plain, eolian, etc. But when -their uses are considered a very different classification -is made, based mostly on their composition, -and we speak of China clays or kaolins, fire -or refractory clays, paving-brick clays, sewer-pipe, -stone-ware, brick, gumbo and slip clays.</p> -<p>The <b>kaolin</b> or <b>china clays</b> are residual clays, -usually resulting from the decomposition of -pegmatite dikes. They must be white when -burned, free from iron oxides, and fairly plastic. -A good deal of china clay is made by crushing -feldspar.</p> -<p><b>Ball clays</b> are sedimentary clays which remain -white when burned, are usually very plastic, and -free from iron oxides. They are mostly used in -the making of various sorts of china.</p> -<p><b>Fire clays</b> may or may not have iron oxides in -them, but they must be free or nearly free from -fluxing materials, such as lime, magnesia and the -alkalies (sodium and potassium compounds). -They may be more or less plastic, the essential -quality being their ability to withstand high temperatures -without fusing. Silica (as sand) tends -to diminish the refractory quality; so that a clay -otherwise suitable, if it has sand in it, becomes at -<span class="pb" id="Page_209">209</span> -best a second grade fire clay. In coal mining -sections it is customary to term those beds of clay -either above or below the coal, “fire clay”; but -this is an unfortunate designation, for though -some of them are true fire clays, the most of them -are not.</p> -<p><b>Stone-ware clays</b> are those with considerable -sand and up to five per cent of fluxing materials. -They must be plastic enough to be readily -worked, and then burn to a dense body at comparatively -low temperatures.</p> -<p><b>Sewer-pipe clays</b> must be plastic, and carry -a considerable amount of fluxing material, as the -surface of the pipe is expected to vitrify in the -burning.</p> -<p><b>Brick clays</b> are low grade clays and vary greatly -in composition. The main requisites are that -they mould easily and bake hard at relatively -low temperatures with as little warping and -cracking as possible. As most clays shrink both -in the air drying and in the baking, sand is added -when the clay is being mixed. The color is -mostly due to the presence of iron impurities. -If there are iron oxides and little or no lime, the -brick bakes to a red color, but if there is an excess -of lime over the iron oxides, it bakes to a cream -or buff color, which on vitrifying turns green.</p> -<p><b>Paving-brick clays</b> range from surface clays, -to semirefractory clays, shale being often used. -The essential component is enough fluxing material, -so that the bricks shall begin to vitrify, or -fuse, at not too high temperatures.</p> -<p><b>Slip clays</b> are those with a high percentage of -fluxing material; so that, when baked at moderate -<span class="pb" id="Page_210">210</span> -temperatures, the surface fuses into a glassy -brown or green glaze.</p> -<p><b>Adobe</b> is an impure calcareous clay, widely -used in the western United States for making -sun-dried bricks.</p> -<p><b>Gumbo</b> is a term applied to fine-grained plastic -clays which shrink too much in the burning to -be useful in manufactures. They can be burned -to make an excellent ballast for railroads and -highways. They are especially abundant in the -Middle Western States.</p> -<h3><a id="species_Loess">Loess</a></h3> -<p>This is the name given to a fine -grained homogeneous clay-like material, -which is a mixture of clay, fine angular -fragments of sand, flakes of mica and more or -less calcareous matter. It is usually without -stratification, and cleaves vertically, so that, -when eroded, it forms steep cliffs. Loess covers -great areas in the Mississippi Valley, in the Rhine -Valley, and in North Central China. By some -it is thought to be an accumulation of dust in -those regions where the prevailing winds were of -diminished velocity and where the grass or other -vegetation has served to catch and hold the -material; by others it is thought of as a river -and lake deposit; and by still others it is thought -to be due to the combination of the two modes, -wind and flood. The writer inclines to the first -view expressed.</p> -<h3><a id="species_Shale">Shale</a> -<br /><a href="#Plate_59">Pl. 59</a></h3> -<p>When pure or impure clays, or -loess, are consolidated, they are all -grouped under the name shale. It -usually possesses a layered or stratified structure, -<span class="pb" id="Page_211">211</span> -which makes it possible to split it into thin -layers. Of all the sedimentary rocks shale is the -commonest, and it may occur in all the places -where clay could occur, but the most widely -distributed shale is that which made the sea -bottom of former times and is more or less calcareous, -like the piece on <a href="#Plate_59">Plate 59</a>, in which bits -of shells are still visible. Shale has the same -wide variation in composition as has clay, the -various types being designated according to the -impurity which is present, as:</p> -<p><i>argillaceous shale</i>, made mostly of clay,</p> -<p><i>arenaceous shale</i>, shale with more or less sand -as an impurity,</p> -<p><i>calcareous shale</i>, or one with more or less lime -as an impurity,</p> -<p><i>ferruginous shale</i>, or one with iron compounds -as impurities,</p> -<p><i>bituminous shale</i>, or one colored black by the -presence of organic matter, remains of either -plants or animals.</p> -<p>While of no value as building material, shale -may be ground or crushed, and used as a substitute -for any corresponding clay, and thus many -manufacturers use shale in making fire-clay -products, bricks, tile, etc.</p> -<h3><a id="species_Marl">Marl</a></h3> -<p>Where limestones or shells of any -sort have been pulverized, and -mixed with more or less impurities, especially -clay, the resulting unconsolidated mass is known -as marl. It is usually associated with marine -formations, and is the finer débris which has -settled on the ocean bottom well out from shore, -<span class="pb" id="Page_212">212</span> -that is out beyond the sandy and mud deposits. -Finding it therefore usually indicates a sea -bottom recently elevated. It is very characteristic -of the southern coastal states, from -Maryland all along to Texas.</p> -<h3><a id="species_Limestone">Limestone</a></h3> -<p>Any mass of marl, or aggregate of -calcareous shells, corals, etc., which -has become consolidated is known as limestone. -It may, and usually does, have a wide range of -impurities, chief of which are clay, sand, iron -oxides, and bituminous matter, like plant or -animal remains. Pure limestone is white, but -due to impurities it ranges through grays, greens, -browns, to black, and even red, but this last is -rarer. It is easily identified by the presence of -calcium carbonate, which effervesces in hydrochloric -acid. It most often represents deposits -in fairly deep water on ocean bottoms of the past, -but there is also a wide range of limestones -which were formed in fresh water.</p> -<p>Limestone is often burned at temperatures -just above 900° C, at which point carbon dioxide -goes off as a gas, and leaves calcium oxide, or -lime. When this is mixed with water it makes -calcium hydroxide, or slaked lime, which is -mixed with sand to give it body, and is used as -mortar. When exposed to the air, the slaked -lime gives up water, and takes back from the air -carbon dioxide, and again becomes calcium -carbonate with its original hardness. Limestone -is also used as one of the elements in all cements. -It is also considerably used as a building stone, -which, however, suffers in moist climates from -<span class="pb" id="Page_213">213</span> -the solution of its lime by rains, but has stood up -very well in dry climates.</p> -<p>The varieties of limestone are mostly distinguished -according to their mode of origin, -some of them being as follows.</p> -<p><b>Bog Lime</b> is a white calcareous powdery deposit -on the bottom of ponds in limestone regions, -a deposit precipitated from solution by the -action of the plants inhabiting the ponds.</p> -<p><b>Coquina</b> (<a href="#Plate_59">Plate 59</a>) is the rock formed by the -rather loose consolidation of shells and shell fragments. -It is particularly characteristic of tropical -regions, and is very abundant near St. -Augustine, Fla., in which region it was, and still -is, cut into blocks and used for building stone. -In that mild climate it has stood very well.</p> -<p><b>Chalk</b> (<a href="#Plate_60">Plate 60</a>) is a soft fine-grained limestone, -formed in the ocean by the accumulation -of myriads of the tiny shells of Foramenifera, -which are single celled animals, living either a -floating life near the surface of the sea, or a -creeping life on the bottom. Chalk is composed -mostly of the shells of floating Foramenifera, -which when the animals died, settled to the -bottom and there accumulated, mostly at depths -of 600 feet or more. When the mass of unconsolidated -shells is dredged up from depths of -50 to 2000 fathoms, it is known as <i>Foramenifera -ooze</i>. Chalk beds are then indications of an -uplifted sea bottom. When consolidated, if -pure or nearly so, it makes a white chalk, and the -beds may be of considerable thickness, as is the -case of the famous cliffs near Dover on either -side of the English Channel. One of Huxley’s -<span class="pb" id="Page_214">214</span> -most famous lectures is the one on chalk, found -in his <i>Essays and Lay Sermons</i>.</p> -<p><b>Coral Rock</b> is made by the cementation of fragments -of corals. The binding material, as in most -stones, is lime; and this sort of rock is associated -with coral reefs of either the past or the present. -One of the best illustrations of this being the -“Dolomite Mountains” in Tyrol. Coral rock, -like coquina, has been cut into blocks and used as -building stone, as in Bermuda.</p> -<p><b>Encrinal Limestone</b> (<a href="#Plate_60">Plate 60</a>) is a rock made -by the cementation of fragments of the skeleton -of crinoids. These animals belong to the group, -echinoderms, and are now extinct except for a -few so called “sea-lilies.” They were animals -with a central mouth surrounded by long, jointed, -flexible arms in multiples of five, and below this a -small body inclosed in calcareous plates, all at -the top of a long jointed stem. They lived in -the sea and in the earlier geological times must -have been very abundant; for their remains are -so common in places as to make whole layers of -limestone.</p> -<p><b>Hydraulic Limestone</b> is a fine-grained, compact, -yellowish limestone with from 13 to 17% -of sand, and some clay; which, when it is burned -at a temperature a little higher than that used in -burning lime, makes a product, that, while not -as strong as Portland cement, still like it sets -under water.</p> -<p><b>Lithographic Limestone</b> is a very fine-grained, -compact limestone with clay impurities, the -finest of the grain making it usable for making -the stone plates used in lithographic printing. -<span class="pb" id="Page_215">215</span> -On slabs of this limestone figures are drawn in -reverse with a special crayon. Then the slab is -treated with acid, those parts which are not protected -by the drawing being etched away, while -the points protected by the drawing remain in low -relief. From this slab figures can then be printed.</p> -<p><b>Travertine</b> is a general name, applied to calcareous -deposits from fresh water lakes or -streams, and has been precipitated either as a -result of cooling or evaporation. Some travertines -are porous, while others are dense; some are -white, while others are colored, often beautifully, -by impurities in the water.</p> -<p>Porous deposits of travertine, when made on -grass or other like substances, are known as tufa -or <i>calc sinter</i>. Such masses are common around -Caledonia, N. Y., Mammoth Hot Springs in the -Yellowstone Park, etc.</p> -<p><b>Onyx marble</b> is a dense travertine, usually -formed as a result of the deposition of lime from -the water of springs. It is often banded, due -to the presence of impurities in the water at one -time, and their absence at other times.</p> -<h3><a id="species_Till">Till</a></h3> -<p>Till is an unconsolidated mass of -boulders, pebbles, sand and fine clay, -the unsorted material left behind by glaciers -when they melted. The boulders and pebbles, -while they show some wear, are not rounded like -those that have been transported by streams, -but have a more or less angular shape; and some -of them are polished or striated on one side, -where, while frozen in the ice, they were rubbed -along the bottom.</p> -<div class="pb" id="Page_216">216</div> -<p>One of the most recent geological events in -America was the extension of the ice sheet, now -covering Greenland, down over north and northeastern -North America, until it extended as far -south as northern New Jersey, the Ohio River -and the Missouri River, and as far west as the -Rocky Mountains, but not over the Great Basin, -the Cascade Ranges or Alaska. This great -mass of ice, thousands of feet thick, moved from -two centers, one either side of Hudson Bay, -scraping up the loose soil, and grinding off the -exposed surfaces of the underlying rock. All -this material it carried southward, until the -melting along its lower margin equaled the rate -at which it advanced. When the melting was -faster than the advance the glacial sheet retreated. -At the southern limit of the advance -this débris was dropped, either making long ridges -(moraines) or while the ice was retreating, thicker -or thinner sheets. This deposited débris is till.</p> -<p>The soil, and especially the subsoil, in all the -regions formerly covered by the ice sheet, is made -up very largely of this till; which, where it is -undisturbed is often called “hardpan.” When -till is mixed with humus it becomes loam. This -mixture of material, varying all the way from the -fine powdered products of the ice grinding -to the great boulder it picked up and carried -south, is characteristic of this or any other -glaciated country. When this section of country -was settled, the boulders and stone were a hindrance -to cultivation, and were picked up and -piled into stone walls, which are one of the first -features to strike the eye.</p> -<div class="pb" id="Page_217">217</div> -<h3><a id="species_Tillite">Tillite</a></h3> -<p>When till is consolidated into solid -rock, it is known as tillite. In -several cases it has been found buried far beneath -the more recent sedimentary rocks; testifying -that there were other glacial periods beside the -last one which furnished the till.</p> -<h3 class="center"><span class="sc">The Coal Series</span></h3> -<p>Disregarding minor constituents, the plants -are largely made up of cellulose, which is a -combination of carbon, hydrogen, and oxygen, -(C₆H₁₀O₅). If this is heated in the air, where -there is plenty of oxygen, it disintegrates, or -burns, making carbon dioxide and water; but if -the heating is done where the oxygen is excluded, -as in a kiln, the hydrogen and oxygen -will be driven off and the carbon will remain -behind as charcoal. In Nature similar reactions -go on, but more slowly. Vegetable matter, -exposed to the air, disintegrates into carbon -dioxide and water, and there is no solid residue. -However, if the vegetable matter is under -water, which excludes the air more or less -completely including the oxygen in it, then -disintegration still takes place, but the products -formed are water, (H₂O) marsh gas (CH₄), and -some carbon dioxide (CO₂), but a considerable -part of the carbon remains behind and -accumulates.</p> -<p>Thus in bogs, swamps and ponds, where dead -vegetation, especially that growing in the water, -piles up, the oxidation is incomplete; so that -there gradually accumulates on the bottom a -<span class="pb" id="Page_218">218</span> -layer of brown to black mud, known as <i>peat</i>. -More plant remains are constantly being added, -and the layer may increase to several feet in -thickness. The decomposition is incomplete -and some oxygen and hydrogen remain, but the -carbon is in a constantly increasing ratio and -in proportion far above that in cellulose. In -the cold northern climates sphagnum moss is -the most efficient peat producing plant, but in -temperate and tropical climates the moss is -replaced by the leaves, twigs, trunks, etc., of -trees, bushes, and vines.</p> -<p>If these peat beds are buried beneath a layer or -layers of sediment, especially clay, the peat is -sealed up and oxidation stops almost entirely. -With the pressure of the superincumbent beds, -the peat becomes more and more compact, and -changes to a dark-brown or black color. It is -then known as <i>lignite</i>. If this lignite is buried -still deeper, with consequently more pressure -and more time, it changes into the still denser -black <i>bituminous coal</i>. This is as far as it will -go unless some new agent is added to the forces -already working.</p> -<p>The next step in the series of changes forming -coal is associated with mountain making. In -case the layers of rock containing beds of coal are -folded, and that presupposes at least a moderate -increase in heat, the bituminous coal is altered -to <i>anthracite</i>, which is still denser, and so hard -that it breaks with a conchoidal fracture. -Alteration may be carried a step still farther, -in case the rocks between which lie beds of coal -are effected by such high temperatures as accompany -<span class="pb" id="Page_219">219</span> -metamorphism. Then all the associated -hydrogen, oxygen and moisture are driven -off, and only the carbon remains, which is -then known as <i>graphite</i>. All steps between -the stages especially designated occur. The -following represent steps only in the series of -changes.</p> -<h3><a id="species_Peat">Peat</a></h3> -<p>Peat is a mass of unconsolidated -vegetable matter, which has -accumulated under water, and in which the -original plant remains are still, at least in part, -discernible. It contains a large amount of -water, so that before it can be used as a fuel, it is -cut out in blocks, which are piled up and left -for a time to dry before using. It burns with a -long flame and considerable smoke. This country -is so well supplied with other fuels, that so -far peat has been but little used.</p> -<h3><a id="species_Lignite">Lignite</a> -<br /><i>brown coal</i></h3> -<p>Lignite is more compact than -peat, and is found buried to some -depth under layers of clay or sandstone. -It is dark brown to black in color, and -still retains pretty clear traces of the plants -from which it was derived. It also usually contains -a considerable amount of moisture, and -when this is dried out, it tends to crumble badly, -so that it is undesirable to handle it much, or to -ship it far, before using. It has a fair fuel value -and is fairly widely used; but it is very desirable -that some method be found, by which lignite -could be treated to obtain its by-products, and at -the same time make it more compact, so it would -<span class="pb" id="Page_220">220</span> -not crumble with the handling incident to using -it in furnaces. There are extensive lignite -deposits in this country in North and South -Dakota, Montana, Wyoming, Colorado, New -Mexico, Texas, Louisiana, and Mississippi.</p> -<h3><a id="species_BituminousCoal">Bituminous Coal</a> -<br /><i>soft coal</i></h3> -<p>This type of coal is compact, black -in color, and breaks readily, but does -not crumble as badly as lignite. It -contains considerable water, and still has some -hydrogen and oxygen compounds in it. Bituminous -coal is the product of plant remains -which have been preserved for long periods, -(millions of years), sealed from the air by the -overlying beds of rock. The pressure has made -it compact, and nearly all traces of the original -plants have disappeared.</p> -<p>Bituminous coal is our most abundant fuel, -occurring the world over in seams from less -than an inch in thickness to some over fifteen -feet thick. The United States is peculiarly -fortunate in the abundant and easily accessible -deposits of this type of coal, in Pennsylvania, -West Virginia, Ohio, Kentucky, Tennessee, -Indiana, Illinois, Michigan, Iowa, Missouri, -Kansas, Nebraska, Texas, Utah, and Colorado.</p> -<p>The volatile constituents, hydrogen and oxygen -compounds, of bituminous coal may be -driven off by heating the coal in closed ovens, -and the residual mass is known as <i>coke</i>, almost -pure carbon. This is distillation, and the ovens -in which this is done, without trying to save the -volatile products, are called bee-hive ovens, -while the more modern ovens which save the -<span class="pb" id="Page_221">221</span> -by-products are called by-products ovens. A -ton of bituminous coal treated in the typical -by-products oven, will yield on the average 1410 -lb. of coke, 7.1 gallons of tar, 18.9 pounds of -ammonia sulphate, etc., 2.4 gallons of light oils, -10440 cubic feet of illuminating gas, about half -of this last being used to furnish the heat for -the distillation. The coal-tar dye industry is -built on the tar thus produced. Toluol, benzol, -etc., come from the light oils; and half the gas -produced is available for household illumination, -etc. Coke is demanded, as it is a superior fuel -for melting iron ores, iron and steel, and is made -regardless of whether the by-products are used. -The coke thus produced is hard, clean, and -vesicular; but for some reason as yet unknown, -by no means all bituminous coal will produce a -coke which has this porous structure. These -latter are known as “non-coking,” and are of -little use to the steel industry.</p> -<h3><a id="species_CannelCoal">Cannel Coal</a></h3> -<p>This is a compact variety of non-coking -bituminous coal, with a dull -luster and a conchoidal fracture. It -contains the largest proportion of volatile hydrocarbon -compounds of any variety of coal; so that -when the supply of petroleum and natural gas -gives out, this will be one of the important -sources of obtaining substitutes. Cannel coals -occur in Ohio, Indiana, and eastern Kentucky. -This cannel coal owes its peculiar fatty nature -to the material from which it is derived, it being -supposed to have resulted from the accumulation -of the spores of lycopod trees, and their conversion -<span class="pb" id="Page_222">222</span> -to jelly-like masses by bacteria in the -fresh-water marshes of those ancient days.</p> -<h3><a id="species_Anthracite">Anthracite</a> -<br /><i>hard coal</i></h3> -<p>Anthracite coal is hard, black, -has a luster, and breaks with a -conchoidal fracture. It contains but -a low percentage of volatile matter, and so burns -with a short flame, and less smoke, than is the -case with the other coals. It is always associated -with folded rocks, and appears to have -been formed as a result of the combined pressure -and the higher temperatures, which accompanied -mountain making. Still the temperature was -not high enough to metamorphose the adjacent -rocks. Most of our anthracite comes from -northeastern Pennsylvania.</p> -<h3><a id="species_Carbonite">Carbonite</a></h3> -<p>Carbonite is natural coke. It -occurs in coal seams which have been -cut by dikes or intrusions of igneous rocks, the -coal having been thus coked by natural processes. -It is not vesicular like artificial coke, for which -reason it is not useful as a fuel. Some carbonite -is found in the Cerillos coal field of New Mexico, -in Colorado, and Virginia.</p> -<h3><a id="species_Jet">Jet</a></h3> -<p>Jet is a dense variety of lignite, a -fossil wood of black color, which -takes a high polish and cuts easily into various -ornamental shapes. It has been used for -ornaments since early ancient times, beads of jet -being found in the early bronze period in England, -the supply probably coming from the -Yorkshire coast, whence the principal supply -<span class="pb" id="Page_223">223</span> -comes even to the present day. In Switzerland -and Belgium it was used still earlier, even as far -back as the Palæolithic age. Jet seems then -to have had a talismanic value, and to have been -worn to protect the owner. About 700 <span class="small">A.D.</span> crosses -and rosaries began to be made of jet, the custom -starting at Whitby Abbey, the material being -obtained nearby, so that it came to be known as -“Whitby jet,” and in the eighteenth century became -very popular. In recent times it has been -used mostly as jewelry suitable for mourning.</p> -<h3><a id="species_Amber">Amber</a> -<br /><a href="#Plate_61">Pl. 61</a></h3> -<p>Amber is a gum which oozed from -coniferous trees and was petrified. -It is associated with lignite beds of -middle Tertiary age. It is usually pale-yellow -in color, but at times has a reddish or brownish -tinge, and is more or less transparent. It -occurs in rounded irregular lumps, up to ten -pounds in weight, though most pieces are -smaller; and is mostly picked up along certain -coasts where it is washed ashore by the waves. -Since the earliest records amber has been cast -up on the shores of the Baltic, and it was used by -peoples as early as in the stone age for ornaments -and amulets. It has been found among -the remains of the cave dwellers of Switzerland, -in Assyrian and Egyptian ruins of prehistoric -age, and in Mycenæ in the prehistoric graves of -the Greeks, the first recorded reference to it being -in Homer, and the Greek name for amber being -<i>elektron</i> from which our word electricity comes. -All these finds were of Baltic amber which was -doubtless gathered and traded by those early -<span class="pb" id="Page_224">224</span> -men. Even down to the present many men -make their living, riding along the shore at low -tide and hunting for the amber washed ashore -by the waves. As early as 1860 the German -geologists concluded that the source of the -amber must be lignite beds outcropping beneath -the sea level, and started mining for the -amber with fair success, so that today two types -of Baltic amber are distinguished, “sea stone” -which is washed ashore, and “mine stone” -taken from the mines. Beside the Baltic locality, -it is found along the shores of the Adriatic, -Sicily, France, China, and occasionally of -North America.</p> -<p>Some pieces of amber are found with insects -inclosed and preserved almost as perfectly as if -collected yesterday. They were apparently -entangled in the gum while still viscid and -completely embedded, before fossilization.</p> -<h3 class="center"><span class="sc">The Petroleum Series</span></h3> -<p>Certain sedimentary rocks contain larger or -smaller quantities of natural gas, petroleum, -mineral tar and asphalt. These are compounds -of carbon and hydrogen, or hydrocarbons, and -range from gases to solids, each being a mixture -of two or more hydrocarbon compounds. The -crude petroleum may have either a paraffin base -or an asphalt base: in the former case, when the -gas, gasoline, kerosene, etc., have been removed -by distillation, the solid residue will be paraffin, -as in most of the Pennsylvania crude oils; while -in the latter case, the solid residue will be an -<span class="pb" id="Page_225">225</span> -asphalt, as in most of the California and Texas -crude oils. In the case of the paraffin series all -the compounds belong to the paraffin group, -while the asphalt is due to the presence, in addition -to the paraffin group, of some of the benzine -series of hydrocarbons.</p> -<p>Petroleum is found in sands and shales, which -were originally deposited on ancient sea bottoms, -the shales generally being the real source of the -petroleum. The oil was once the fatty portion -of animal bodies (perhaps to some extent of plant -bodies), and was separated during decomposition -as a result of bacterial activity. Oil thus produced -is in tiny droplets, which have a great -affinity for clay. After being freed by the -bacteria, the oil droplets in muddy water attach -themselves to particles of clay, and as the clay -settles the oil is carried down with it, the two -eventually making a bituminous shale. In clear -water, or in water which is in motion, the oil -droplets rise to the surface and eventually distill -into the air.</p> -<p>The oil, or petroleum, may stay diffused -through the shales, in which case we have <i>oil-bearing -shales</i>, with sometimes as much as 20% -of oil. Were there but ¹/₁₀₀₀ of a per cent of oil -in a layer of shale 1500 feet thick, this would -amount to 750,000 barrels per square mile which -is equal to a rich production from wells. When -the oil in shale amounts to three per cent or more, -it is commercially usable. There are large -stretches of petroleum-bearing rocks in New -York, Pennsylvania, Ohio, Indiana, and all the -way out to the Pacific coast, some of them with -<span class="pb" id="Page_226">226</span> -oil so abundant, that a blow of the hammer will -cause them to smell of petroleum.</p> -<p>In case these oil-bearing shales have been -heavily overburdened and compressed, the -petroleum may have been more or less completely -pressed out of them. Then the droplets -uniting have formed a liquid, which has moved -out from the shale, and gone wherever it could -find open spaces. Sandstones have frequently -offered their pore space, and as it filled, have -been thus saturated with petroleum. If the -sandstones were open to the air, or if fissures -extended from them to the surface, the oil has -escaped to the surface and evaporated into the -air. But in those cases where the sandstone -(or other permeable rocks) was covered by an -impervious layer, like a dense shale or clay, the -oil was confined below the covering layer of -rock. Crude oil is lighter than water; so that -when natural gas, petroleum and water were all -present in the rocks, the gas lies on top, the -petroleum next, and the water underneath. -With this in mind it is easy to see, that in slightly -folded or undulating layers of rock, the gas and -petroleum would be caught under upraised folds -and domes. This is the basis of prospecting for -oil.</p> -<p>If petroleum-bearing layers are depressed far -enough beneath the surface to be affected by the -high temperatures of the earth’s interior, or have -been near volcanic activity, of course the petroleum -has been distilled by natural processes, -and at most only the residues, like paraffin or -asphalt, have remained. For this reason it is -<span class="pb" id="Page_227">227</span> -impossible to find petroleum in igneous or metamorphic -rocks.</p> -<h3><a id="species_NaturalGas">Natural gas</a></h3> -<p>Natural gas is the lightest portion -of crude oil, and consists mostly of -marsh gas (“fire damp,” CH₄) together with other -light hydrocarbons, like ethane (C₂H₆), ethylene -(C₂H₄), and some carbon dioxide and -monoxide. It is colorless, odorless, and burns -with a luminous flame. Mixed with air it is -explosive. It is found in sedimentary rocks, -mostly sandstones, either with or without petroleum. -Usually it is under considerable pressure, -and escapes with great force wherever -a hole permits. In time the gas all escapes -through the hole or well, and then the well -“runs out.” If petroleum is present under -the natural gas, the hole may become an “oil -well,” from which petroleum may be pumped, -until it in turn is exhausted. The end of an -oil supply is usually indicated by the appearance -of water in the well. Natural gas is mostly -associated with oil districts, as in Pennsylvania, -Ohio, Illinois, Texas, California, etc.</p> -<h3><a id="species_PetroleumCrudeOil">Petroleum Crude Oil</a> -<br /><a href="#Plate_61">Pl. 61</a></h3> -<p>Petroleum is a mixture of paraffin -compounds all the way from the -gases, through gasoline, kerosene, -lubricating oils, and vasoline to paraffin. In -some of the crude oils there is also an admixture -of compounds from the benzine series, in which -case, when all the volatile compounds have been -distilled off, an asphalt remains. The different -components of petroleum may be separated out -<span class="pb" id="Page_228">228</span> -by heating the crude oil in closed tanks, and -drawing off the various substances at the proper -temperatures.</p> -<p>Petroleum occurs in sedimentary rocks of marine -origin, usually rocks which also contain the -shells of some of the animals, the soft parts of -which made the oil. To have been preserved -the millions of years since the petroleum was -first formed, the oil-bearing layers must have -been covered by some impervious layer of rock, -beneath the domes and anticlines of which the -oil has lain ever since. When such a dome or -anticlinal fold is perforated by a well, the -released oil flows to the surface with a greater or -less rush, according to the pressure. Wells may -keep flowing for 20 years, sometimes more, sometimes -much less. Those which flow with the -greatest pressure usually are relatively short -lived, at times lasting only a year or two. When -this easily obtained oil is exhausted, there is an -even greater supply to be obtained by the distillation -of the bituminous shales. Petroleum -never occurs in igneous or metamorphic rocks, -but is found in either sandstones or shales, in -places favorable for accumulation, all across that -great stretch of ancient sea bottoms, extending -from the Appalachian Mountains to the Rocky -Mountains, and in the Great Basin between the -Rocky Mountains and the Sierra Nevada Range, -and also to the west of the Sierras.</p> -<h3><a id="species_Bitumen">Bitumen</a></h3> -<p>Where petroleum has escaped -through pores in the rocks, or by way -of fissures, and has come to the surface of the -<span class="pb" id="Page_229">229</span> -earth, the lighter components, thus exposed to -the air, have vaporized and escaped, leaving -behind a more or less solid residue, which is -known as bitumen. If the escape was through a -fissure, the bitumen may have accumulated in -the fissure until it was filled, making vein bitumen. -Or the escape may have been so rapid that -the petroleum formed a pool or lake from the -surface of which evaporation took place. In -time such a pool will give off the gases and -volatile compounds, only a residue remaining -to make a pitch lake, like the one at Rancho Le -Brea near Los Angeles, or an asphalt lake like -the one on the island of Trinidad. On account -of their varying hardness and composition, some -of these bitumens have received special names; as:</p> -<p><b>Albertite</b>, a black bitumen with a brilliant -luster on broken surfaces, a hardness between 1 -and 2, and a specific gravity a shade over 1.</p> -<p><b>Grahamite</b>, a black bitumen, which is brittle, -but has a dull luster, a hardness of 2, and a specific -gravity of 1.15.</p> -<p><b>Gilsonite</b> or <b>Uintaite</b>, a black bitumen with a -brilliant luster and a conchoidal fracture, a -hardness of 2 to 2½, and a specific gravity of -1.06.</p> -<p><b>Malta</b> is a semi-liquid viscid natural bitumen, -which has a considerable distribution in California.</p> -<p>The above varieties of bitumen look a good -deal like coal, but are easily distinguished by -their lightness (weight about half that of coal), -and the fact that with only moderate heat they -melt, and become a thick liquid like tar.</p> -<div class="pb" id="Page_230">230</div> -<h3><a id="species_Guano">Guano</a></h3> -<p>Guano is the accumulation of the -excrement of birds (or of other animals -like bats) on areas so dry that, though -soluble, it is not leached and washed away. It -may also contain some of the bones and mummified -carcasses of the birds which died on the spot. -The greatest of these deposits are on several small -islands, just off the west coast of Peru, and now -“farmed” by the Peruvian government. In this -country there are no true guano beds, except a -few accumulations of bat guano in certain caves -of Kentucky and Texas, but these are not large -enough to become of commercial importance.</p> -<h3><a id="species_PhosphateRock">Phosphate Rock</a></h3> -<p>Phosphate rock is one composed -chiefly of calcium phosphate along -with various impurities, such as clay -and lime. It occurs in beds, irregular masses, -or as concretionary nodules in limestone or sand.</p> -<p>The bedded varieties are in the older sedimentary -rocks, in which the phosphate runs -from a small percentage up to as high as 85%. -Ultimately the phosphate came from either -animal excrement, or from bacterial decomposition -of animal carcasses and bones. In all the -beds it seems to be true that in the first instance -the phosphate was laid down as a disseminated -deposit in marine beds, usually limestones. -Later by the action of water leaching through -the rocks, the phosphate was dissolved, and then -redeposited elsewhere in a more concentrated -form. This may be either in the underlying -sandstones, but is more often in limestones, -replacing the original lime.</p> -<div class="pb" id="Page_231">231</div> -<p>In these secondary deposits, if the phosphate -has been laid down in cavities, the resulting -phosphate will be in nodular masses. In the case -of the Florida and Carolina deposits, these -nodules have been freed from their matrix and -washed along the river beds, remaining as -pebbles in the river sands. The bed deposits -are mostly in Kentucky and Idaho. The commercial -use for such phosphate rocks is of course -the making of fertilizers.</p> -<h3><a id="species_DiatomaceousEarth">Diatomaceous Earth</a> -<br /><a href="#Plate_62">Pl. 62</a></h3> -<p>Diatoms are tiny single-celled -plants living in uncounted millions -in the fresh and salt water. Each -diatom builds around itself two shells which fit -into each other like the cover and box of a pill-box, -and each shell is marvelously ornamented. -The shells are composed of silica of the opal -type. In size the diatoms range from ¹/₅₀₀₀ of an -inch in diameter up to the size of a pin head, and -they live in such numbers that ordinary surface -waters have hundreds of them to the quart, and -where they are flourishing up to 250,000 in a -quart. When the plants die, or in order to -reproduce abandon the shells, these shells fall -to the bottom of the pond or the sea, and there -accumulate, often making a layer from a few -inches thick up to hundreds of feet in extreme -cases. If unconsolidated, this mass of tiny -shells is known as diatomaceous earth; but if -they are consolidated it is called tripolite, so -named because the first of them used commercially -came from Tripoli.</p> -<p>As the shells are tiny and uniform in size and -<span class="pb" id="Page_232">232</span> -have a hardness of 6, the diatomaceous earth is -used to make a great variety of polishes, scouring -soaps, tooth paste, as a filler in certain kinds of -paper, in making waterglass, as an absorbent for -nitroglycerine, and as packing in insulating compounds, -where asbestos would otherwise be used.</p> -<p>Deposits of freshwater diatoms are found all -over the United States, usually in thin layers of -limited extent, especially in Massachusetts, New -York, Michigan, etc. The marine deposits of -diatoms are on a much larger scale, there being -beds of diatoms in Anne Arundel, Calvert and -Charles Counties, Md., up to 25 or 30 feet in -thickness. In Santa Barbara County, Cal., -there is one bed 2400 feet thick and another 4700 -feet thick, beside many other smaller ones. The -enormous former wealth of life indicated by these -great deposits may be suggested, when it is -remembered that it takes about 120,000,000 to -make an ounce in weight. They reproduce on an -average about once in five days, so that from a -single diatom the offspring possible under favorable -conditions would amount to over 16,000,000 -in four months or over 60 tons in a year. Of -such an order is the potential increase of animals -or plants, no matter how small, if the rate of -reproduction is high.</p> -<h3 class="center"><span class="sc">Metamorphic Rocks</span></h3> -<p>Either a sedimentary or an igneous rock, -which has been altered by the combined activities -of heat, pressure and chemical action, -becomes a metamorphic rock. The process is -<span class="pb" id="Page_233">233</span> -essentially one, during which the layers of rock -come under the influence of such temperatures -as are associated with the formation of granite -or lavas. Such material as is actually melted -becomes igneous rock, but adjacent to the -masses actually melted are other rocks which do -not melt but, according to the temperature, are -more or less changed, and these are the metamorphic -rocks. At a distance from the molten masses -the changes are minor, but close to the molten -magmas extensive changes take place. Though -not actually melted the rock near the heat center -may be softened, usually is, in which case pebbles -and grains or even crystals become soft and plastic, -and, as a result of the great pressure, are -flattened, giving the rock, when it cools again, a -striated appearance. At these high temperatures -the water in the rock and also some other -substances vaporize, and the hot steam and -vapor are active agents in making a great many -chemical changes. In some cases material like -clay is changed into micas, or chlorite, etc.; in -other cases the elements of a mineral will be -segregated and large crystals will appear -scattered through the metamorphic rock, such as -garnets, staurolites, etc.</p> -<p>If one studies a layer of rock both near and far -from the molten mass, all grades of change will -appear. For example, at a distance a conglomerate -maybe unaltered; somewhat nearer the -molten mass, the heat and steam may have softened -(but not melted) the pebbles and then the -pressure has flattened them as though they were -dough; and nearest the molten mass, the outlines -<span class="pb" id="Page_234">234</span> -of the pebbles are lost, only a layered effect -remaining, and many of the materials have -changed into new minerals, like mica, garnets, -etc., but still the layered effect is preserved.</p> -<p>One of the effects of heat and pressure is to -flatten the component particles of the rock, so -that it tends to split in a direction at right angles -to the direction of the pressure, just as particles -of flour are softened and flattened under the -pressure of the roller; and then when the crust -is baked it splits or cleaves at right angles to -the direction in which the pressure was exerted -by the roller. This tendency to split is not to be -confused with either the layering, characteristic of -sedimentary rocks, nor the cleavage characteristic -of minerals. It has nothing to do with the -way the particles were originally deposited, nor -with their cleavage; but is due to the pressure, -and resembles the pie crust splitting, being -irregular and flaky. This is designated <i>schistosity</i> -if irregular and <i>slaty cleavage</i> if regular. -Schistosity refers to the flaky manner of splitting -into thin scales as in mica schists. Slaty -cleavage is more regular, this being due to the -fact that the material of which slate is made is -small particles of clay of uniform size.</p> -<p>The metamorphic rocks are generally more or -less folded, as they are always associated with -mountain making. These major folds are of -large size, from a hundred feet across to several -miles from one side to the other. Such folds may -also occur in sedimentary rocks or even in igneous -rocks and simply express the great lines of yielding, -or movement of the crust of the earth. In -<span class="pb" id="Page_235">235</span> -addition to this there is minor folding or contorting -which is characteristic of metamorphic rocks -only. When the rocks were heated by their -nearness to the molten igneous magmas, they -must expand, but being overburdened by thick -layers of other rocks, there is no opportunity for -yielding vertically, so the layers crumple, making -minor folds from a fraction of an inch to a few -feet across. Such crumpling, which is so very -conspicuous especially where there are bands of -quartzite in the rock, is entirely characteristic of -metamorphic rocks. It is seen on hosts of the -rocks about New York City, all over New England, -and in any other metamorphic region. -<a href="#Plate_63">Plate 63</a> is a photograph of such a crumpled rock -which has been smoothed by the glacial ice.</p> -<p>The metamorphic rocks are the most difficult -of all the rocks to determine and understand, -because the amount of change through which -they have gone is greatest, but for this same -reason they offer the most interest, for the -agents which caused the changes are of the most -dramatic type of any that occur in Nature. -From one place to another a single layer of metamorphic -rock changes according to the greater -or less heat to which it was subjected, making -a series of related rocks of the same composition -but with varied amount of alteration. For this -reason in naming metamorphic rocks, a type is -named, and from that there will be gradations -in one or more directions, both according to -composition, and according to amount of heat -involved. If it is possible to follow a given layer -of metamorphic rock from one place to another -<span class="pb" id="Page_236">236</span> -this is of great interest; for by this means, many -variations in the type will be found, both those -resulting from a different amount of heat, and -those due to the local changes in the composition -of the original rock.</p> -<p>One further consideration has to be kept in -mind. When a rock is metamorphosed the -high temperatures either drive off all water, or -the water may be used up in the making of some -of the complex minerals. When such a metamorphic -rock later comes near the surface and is -exposed to the presence of ground water, and -that leaching down from the surface into the -rocks, several of the minerals formed at high -temperatures will take up this water and make -new minerals such as serpentine, chlorite, etc. -They are always associated with metamorphic -rocks, and have been metamorphic rocks, but -since then have become hydrated, forming minerals -not at all characteristic of high temperature.</p> -<p>The following shows the relation of the -sedimentary and igneous rocks to their metamorphic -equivalents.</p> -<table class="center" summary=""> -<tr class="th"><th><i>Loose sediment</i> </th><th><i>Consolidated sediment</i> </th><th><i>Metamorphic equivalent</i></th></tr> -<tr><td class="l"><a href="#species_Gravel">gravel</a> </td><td class="l"><a href="#species_Conglomerate">conglomerate</a> </td><td class="l"><a href="#species_Gneiss">gneiss</a></td></tr> -<tr><td class="l"><a href="#species_Sand">sand</a> (<a href="#species_Quartz">quartz</a>) </td><td class="l"><a href="#species_Sandstone">sandstone</a> </td><td class="l"><a href="#species_Quartzite">quartzite</a></td></tr> -<tr><td class="l">mud (<a href="#species_Sand">sand</a> and <a href="#species_Clay">clay</a>) </td><td class="l"><a href="#species_Shale">shale</a> </td><td class="l"><a href="#species_Schist">schist</a></td></tr> -<tr><td class="l"><a href="#species_Clay">clay</a> </td><td class="l"><a href="#species_Shale">shale</a> </td><td class="l"><a href="#species_Slate">slate</a> or <a href="#species_Phyllite">phyllite</a></td></tr> -<tr><td class="l"><a href="#species_Marl">marl</a> </td><td class="l"><a href="#species_Limestone">limestone</a> </td><td class="l"><a href="#species_Marble">marble</a></td></tr> -<tr><td class="l"><a href="#species_Peat">peat</a> </td><td class="l"><a href="#species_BituminousCoal">bituminous coal</a> </td><td class="l"><a href="#species_Anthracite">anthracite</a> to <a href="#species_Graphite">graphite</a></td></tr> -<tr><td class="l"> </td><td class="l">coarse igneous rocks such as <a href="#species_Granite">granite</a>, <a href="#species_Syenite">syenite</a>, etc. </td><td class="l"><a href="#species_Gneiss">gneiss</a></td></tr> -<tr><td class="l"> </td><td class="l">fine igneous rocks such as <a href="#species_Trachite">trachite</a>, <a href="#species_Rhyolite">rhyolite</a>, etc. </td><td class="l"><a href="#species_Schist">schist</a></td></tr> -</table> -<div class="pb" id="Page_237">237</div> -<p>In working out the past history of any given -region, much of it is done on the basis of this -series of equivalents. The finding of limestone, -for instance, indicates that the given area was -at one time under the sea to a considerable depth, -that is from 100 to 1000 feet, but not ocean-bottom -depths which run in tens of thousands of -feet. Marble indicates the same thing, and so -one can go on through all these types of rock.</p> -<h3><a id="species_Gneiss">Gneiss</a> -<br /><a href="#Plate_64">Pl. 64</a></h3> -<p>Gneiss is an old word used by the -Saxon miners, and is often very -loosely used. Here it is used in its -structural sense, and a gneiss may be defined -as: a banded metamorphic rock, derived either -from a sedimentary or an igneous rock, and is -composed of feldspar, quartz, and mica or hornblende, -and is coarse enough, so that the constituent -minerals can be determined by the eye. -It corresponds to a granite, or some sedimentary -rock like gravel or conglomerate.</p> -<p>Due to the action of pressure, all the gneisses -are banded, and the original constituent particles -or crystals are distorted. The lines of -banding may be long or short, straight, curved or -contorted. When the banding is not conspicuous, -the gneiss tends toward a granite. -When the banding is thin and the structure -appears flaky, the gneiss tends toward a schist. -The color varies according to the constituent -minerals, from nearly white, through red, gray, -brown, or green to nearly black. <a href="#Plate_64">Plate 64</a> shows -one gneiss which is in a less advanced stage, the -pebbles being simply flattened and the matrix -<span class="pb" id="Page_238">238</span> -partly altered to micaceous minerals, and a -second gneiss which is so far advanced that the -original constituents are all altered to other -minerals and only the banded structure remains. -This latter type would have required but little -more heat to have completed the melting and -changed this to a granite.</p> -<p>Gneisses are very compact and have little or -no pore space in them. They are hard and -strong and resist weathering well, so that they -are widely used as building stone: but they are -not as good as granite for this purpose, as they -split more readily in one direction and can not -therefore be worked so uniformly as can -granite.</p> -<p>There are many varieties of gneiss, based -either on their origin, composition, or their -structure, as follows:</p> -<dl class="undent"><dt><b>Granite-gneiss</b> is one derived by metamorphism from granite.</dt> -<dt><b>Syenite-gneiss</b> is one derived by metamorphism from syenite.</dt> -<dt><b>Diorite-gneiss</b> is one derived by metamorphism from diorite.</dt> -<dt><b>Gabbro-gneiss</b> is one derived by metamorphism from gabbro.</dt> -<dt><b>Biotite-gneiss</b> is one composed of quartz, feldspar and biotite.</dt> -<dt><b>Muscovite-gneiss</b> is one composed of quartz, feldspar and muscovite.</dt> -<dt><b>Hornblende-gneiss</b> is one composed of quartz, feldspar and hornblende.</dt> -<dt><b>Banded-gneiss</b> is one in which the banded structure shows clearly.</dt> -<dt><b>Foliated-gneiss</b> is one in which there is thin irregular layering.</dt> -<dt><b>Augen-gneiss</b> is one which has concretionary lumps scattered through it.</dt></dl> -<div class="pb" id="Page_239">239</div> -<p>Gneisses have a wide distribution over all New -England, most of Canada, the Piedmont Plateau, -the Lake Superior region, the Rocky Mountains, -the Sierra Nevada and the Cascade Ranges.</p> -<h3><a id="species_Quartzite">Quartzite</a></h3> -<p>Quartzite is metamorphosed sand -or sandstone, and frequently grades -into one or the other. It is a hard compact -crystalline rock, which breaks with a splintery or -conchoidal fracture. It is distinguished from -sandstone by the almost complete lack of pore -spaces, its greater hardness and by its crystalline -structure. In practice it may be distinguished -by the fact that a sandstone in breaking separates -between the grains of sand, while a quartzite -breaks through the grains.</p> -<p>Some quartzites are almost pure quartz, but -others contain impurities of clay, lime or iron, -which were in the original sandstone. These -alter in the metamorphism to such accessory -minerals as feldspar, mica, cyanite, magnetite, -hematite, calcite, graphite, etc. The color of -quartzite when pure is white, but may be altered -to red, yellow, or green by the presence of these -accessory minerals.</p> -<p>On account of the difficulty of working the -quartzites, they are not much used in building, -though they are very durable. When crushed -they often make excellent road ballast, or filling -for concrete work. The pure varieties are sometimes -<span class="pb" id="Page_240">240</span> -ground and used in the manufacture of glass.</p> -<p>According to the accessory mineral, the following -varieties may be distinguished; chloritic-quartzite, -micaceous-quartzite, feldspathic-quartzite, -etc.</p> -<p>Quartzites are common in the New England, -the Piedmont Plateau, and Lake Superior metamorphic -regions, and also in many western -localities.</p> -<h3><a id="species_Schist">Schist</a> -<br /><a href="#Plate_65">Pl. 65</a></h3> -<p>Schist is a loosely used term, but -is used here in its structural sense. -It includes those metamorphic rocks -which are foliated or composed of thin scaly -layers, all more or less alike. The principle -minerals are recognizable with the naked eye. -In general schists lack feldspar, but there are -some special cases in which it may be present. -Quartz is an abundant component of schists; and -with it there will be one or more minerals of the -following groups: mica, chlorite, talc, amphibole -or pyroxene. Frequently there are also accessory -minerals present, like garnet, staurolite, -tourmaline, pyrite, magnetite, etc.</p> -<p>All schists have the schistose structure, and -split in one direction with a more or less smooth, -though often irregular, surface. At right angles -to this surface they break with greater or less -difficulty and with a frayed edge. As they get -coarser, the schists may grade into gneisses, -losing their scaly structure: while on the other -side, as the constituent minerals become finer -and so small as to be difficult of recognition, -schists may grade into slates.</p> -<div class="pb" id="Page_241">241</div> -<p>The varieties of schist are based on the mineral -associated with the quartz; as mica-schist, -chlorite-schist, hornblende-schist, talc-schist, etc.</p> -<p>The color also is due to the constituent minerals -other than quartz and ranges widely, mica-schists -being white to brown or nearly black, -chlorite-schists some shade of green, hornblende-schists -from dark green to black, talc-schists -white, pale-green, yellowish or gray, etc.</p> -<p>Schists are found all over the same regions as -gneisses and quartzites, <i>i.e.</i>, New England -(especially good exposures of schist being seen -about New York City), the Lake Superior region, -Rocky Mountains, etc. Beside these regions -where it occurs native, there are boulders of -schist all over the glaciated areas of eastern -and northern United States.</p> -<h3><a id="species_Slate">Slate</a></h3> -<p>Slate is a metamorphic rock which -will split into thin or thick sheets, -and is composed of grains so fine as to be indistinguishable -to the unaided eye. The cleavage -is the result of pressure during metamorphism, -and has nothing to do with the bedding or -stratification of the sedimentary rock from -which it was derived. The original bedding -planes may appear as streaks, often more or less -plicated, and running at any angle with the -cleavage. If these bedding streaks are abundant -or very marked, they may make a slate -unsuitable for commercial uses. The slaty -cleavage may be very perfect and smooth so -that the rock splits into fine sheets, in which case -it is often used for roofing slate; but by far the -<span class="pb" id="Page_242">242</span> -greater part of the slates have a cleavage which is -not smooth or perfect enough so that they can be -so used. Slates are the metamorphic equivalents -of shales and muds, and represent the effect of -great pressure but with less heat than is associated -with schists or phyllite, and consequently with -less alteration of the original mineral grains.</p> -<p>The color ranges from gray through red, green -and purple to black. The grays and black are due -to the presence of more or less carbonaceous -material in the original rock, the carbon compounds -having changed to graphite. The reds -and purple are due to the presence of iron oxides, -and the green to the presence of chlorite.</p> -<p>While the particles of slate are so small as to -be indistinguishable to the unaided eye, the use -of thin sections under the microscope shows that -slate is composed mostly of quartz and mica, -with a wide range of accessory minerals, like -chlorite, feldspar, magnetite, hematite, pyrite, -calcite, graphite, etc.</p> -<p>According to their chief constituents slates -may be distinguished as argillaceous-slate or -<i>argillite</i>, bituminous-slate, calcareous-slate, siliceous-slate, -etc.</p> -<p>Slate will be found here and there in the metamorphic -areas of New England, the Piedmont -Plateau, the Lake Superior region, and in many -places in the west.</p> -<h3><a id="species_Phyllite">Phyllite</a> -<br /><a href="#Plate_66">Pl. 66</a></h3> -<p>Phyllite is a thinly cleavable, -finely micaceous rock of uniform -composition, which is intermediate -between slate and mica schist. In this case the -<span class="pb" id="Page_243">243</span> -flakes of mica are large enough to be distinguishable -to the eye, but most of the rest of the -material can only be identified with the aid of a -microscope. It is mostly quartz and sericite. -Phyllite represents a degree of metamorphism -greater than for slate, but less than for schist; -and it may grade into either of these other rocks. -Garnets, pyrite, etc., may be present as accessory -minerals. The color ranges from nearly white to -black, and it is likely to occur in the same places -as do slates.</p> -<h3><a id="species_Marble">Marble</a> -<br /><a href="#Plate_66">Pl. 66</a></h3> -<p>This is a broad term, and includes -all those rocks composed essentially -of calcium carbonate (limestones) or -its mixture with magnesium carbonate (dolomite), -which are crystalline, or of granular -structure, as a result of metamorphism. It -takes less heat to metamorphose a limestone, and -for this reason the marbles have a more crystalline -structure than most metamorphic rocks; -and they do not have the tendency to split or -cleave which is so characteristic of most metamorphic -rocks. It is only when there is a large -amount of mica present that the typical schistosity -appears. Commercially the term marble is -used to include true marble and also those -limestones which will take a high polish; but in -this book, and geologically speaking, no rock is a -marble unless it has crystalline structure.</p> -<p>Marbles range widely in color according to -their impurities. Pure marble is white. Carbonaceous -material in the antecedent limestone -is changed to graphite in the metamorphic -<span class="pb" id="Page_244">244</span> -process, and makes the marble black, but appears -usually in streaks or spots, rather than in -any uniform color. An all black “marble” is usually -a limestone. The presence of iron colors the -marble red or pink. Chlorite makes it green, etc.</p> -<p>Various accessory minerals are common in -marbles, such as mica, pyroxene, amphibole, -grossularite among the garnets, magnetite, spinel, -pyrite, etc., through a long list.</p> -<p>Because it cuts readily in all directions and -takes a high polish, marble is widely used as a -building stone. In the moist climate of the -United States it suffers in being soluble in rain -water when used on the outside of a building: but -for interior decoration it furnishes some of the -finest effects.</p> -<p>The largest marble quarries are developed in -Vermont, Massachusetts, New York, Pennsylvania, -Georgia, Alabama, Colorado, California, -and Washington.</p> -<h3><a id="species_Steatite">Steatite</a> -<br /><i>Soapstone</i></h3> -<p>Steatite is a rock composed -essentially of talc, which is associated -with more or less impurities, -such as mica, tremolite, enstatite, quartz, -magnetite, etc. It is found in and with metamorphic -rocks, and is a rock which has been -modified by hydration from a metamorphic -predecessor. It was probably first a tremolite -or enstatite schist, in which, after the metamorphic -rock came into the zone where ground -water exists, the tremolite or enstatite was -altered to talc, the impurities remaining much -as they were in the first place.</p> -<div class="pb" id="Page_245">245</div> -<p>It is bluish-gray to green in color, often soft -enough to cut with a knife, and has a greasy -feel. It is very resistant to heat and acids; for -which reasons it has proved very useful commercially -in making hearthstones, laundry tubs, -and fire backs; and, when powdered, in making -certain lubricants. The Indians, in the days -before Columbus, took advantage of the ease -with which it is cut, to make from it large pots -for holding liquids, which are today among the -greatest treasures in collections of Indian relics. -They also carved pipe-bowls and various ornaments -and amulets from soapstone.</p> -<p>It is found in Vermont, Massachusetts, New -York, New Jersey, Pennsylvania, Maryland, -Virginia, North Carolina, Georgia and -California.</p> -<h3><a id="species_Serpentine_Rock">Serpentine</a> -<br /><a href="#Plate_67">Pl. 67</a></h3> -<p>Pure serpentine is the hydrated -silicate of magnesium, as described -among the minerals on <a href="#Page_138">page 138</a>. -Serpentine rock is serpentine with more or less -impurities, such as pyroxene, amphibole, olivine, -magnetite, chromite, calcite, magnesite, etc. -It often also contains mica and such garnets as -pyrope, as accessory minerals. Serpentine, like -steatite, always occurs in and with metamorphic -rocks, and was originally a metamorphic rock, -but has since been changed by the hydration of -its silicates, when it came into the zone in which -ground water is present. In the first instance it -was some sort of shale, clay and dolomite, which -was metamorphosed to an amphibole or pyroxene -schist. When this was exposed to the action of -<span class="pb" id="Page_246">246</span> -ground water, the amphibole or pyroxene minerals -were changed to serpentine, resulting in a -rock composed mostly of serpentine, but retaining -the impurities which were in the metamorphic -rock, and perhaps adding to them such -amphiboles and pyroxenes as were not altered -during the hydration process. The above is -the commonest type of serpentine rock. It can -and sometimes has been formed in a similar -way from an igneous predecessor, by the hydration -of its silicate minerals. In this latter case -the serpentine would not be a modified metamorphic -rock, but a modified igneous one. It is -a case where such a rock as a diorite or a gabbro -is exposed to ground water and the pyroxene -present altered to serpentine. A serpentine -formed in this way would be a very impure one.</p> -<p>Serpentine rock is used as an ornamental -stone for interior decoration, because it takes a -high polish and has pleasing colors, various -shades of green. It is however decidedly soft -and will stand very little exposure to weather, -and it is also filled with seams which make it -difficult to get out large slabs.</p> -<p>Serpentine rock occurs fairly commonly in the -metamorphic belt of New England and the -Piedmont Plateau, and in some of the western -states, especially California, Oregon, and -Washington.</p> -<h3><a id="species_Ophiolite">Ophiolite</a> -<br /><i>Ophicalcite</i></h3> -<p>This name is given to marbles -which are streaked and spotted with -serpentine. They are a mixture of -green serpentine and a white or nearly white -<span class="pb" id="Page_247">247</span> -calcite, magnesite or dolomite in variable -proportions.</p> -<p>Ophicalcite occurs in and with metamorphic -rocks, and represents an impure limestone which -has been metamorphised, the lime becoming -marble, and the impurities becoming such silicates -as pyroxene, amphibole, or olivine. This -metamorphic rock has then come into the zone -of ground-water and the silicate minerals have -been changed by hydration to serpentine. Ophicalcite -is then a metamorphic rock, in which -secondary chemical changes have since taken -place. It may have a wide range of accessory -minerals present, such as magnetite, chromite, -pyrope among the garnets, olivine, etc. Verde -antique is a trade name for one of the ophiolites.</p> -<p>While not abundant, ophicalcite is in good -demand as an ornamental stone for interior -work; for it takes a high polish, and is beautiful; -but, on the other hand, it will not stand exposure -to the weather for the calcite is soluble, and there -are numerous seams and cracks in it making it -difficult to obtain large slabs.</p> -<p>It occurs in Quebec, Canada, in the Green -Mountains of Vermont, and in the Adirondack -Mountains.</p> -<div class="pb" id="Page_248">248</div> -<h2 id="c6"><span class="h2line1">CHAPTER V</span> -<br /><span class="h2line2">MISCELLANEOUS ROCKS</span></h2> -<p>There are a few rocks which do not fit into -any of the three groups described, such as concretions, -geodes, meteorites, etc., and they are -gathered together here. There is also one type -of rock, which really belongs among the minerals, -but is likely not to be so recognized at first -glance, and that is the material filling veins. -These last are sometimes designated “vein -rocks,” but are really massive deposits of one, -two or more minerals, and should be referred -to the minerals when found.</p> -<h3 class="center"><span class="sc">Concretions</span></h3> -<p>In the sedimentary rocks there frequently -occur inclusions of a nature different from the -surrounding rock. In shape they are usually -rounded, nodular, spherical, discoidal, ovate, -flattened, elongated or ring-shaped, or combinations -of the foregoing, making often curious and -fantastic forms. In size they range from a -fraction of an inch in diameter to several feet -through. When broken, they may show a -nucleus, around which more or less concentric -<span class="pb" id="Page_249">249</span> -layers have formed, or neither nucleus nor -concentric structure may be visible. The layered -structure of the surrounding rock in some cases -continues right through the nodular mass. -These structures are called concretions, and -their formation in all cases is at least due to -similar reactions.</p> -<p>In general the concretions differ from the -surrounding rock in composition, but are usually -composed of some one of its impurities, of lime -in the clays or silica in limestones, of iron oxide -in sandstone, etc. They seem to have originated -as a result of the solution of the minor mineral, -and then its redeposition around some center or -nucleus. In many cases the nucleus is organic, -such as a leaf, a shell, a bone, etc., so that when -the concretion is split, in its center will be found -the perfect imprint of the leaf, or the shell of a -mollusk, or a bone of a higher animal, sometimes -a whole skeleton. Again the nucleus may -be inorganic like a grain of sand; and in still -other cases no nucleus can be found, though -there was probably one in the beginning. What -has happened is somewhat like the case of accessory -minerals in igneous and metamorphic rocks. -A layer of sediment was laid down, including in -it, here and there, something foreign to the run -of the rock. Later when the water leaches -through this rock, impregnated with lime for -instance, it comes to the point where a leaf is -decomposing. The products of the leaf decomposition -are different from what is already -present in solution, and may precipitate some -of the lime in that neighborhood. As long as leaf -<span class="pb" id="Page_250">250</span> -decomposition continues the precipitation in -that region will continue and increase the size -of the concretion. This sort of action accounts -for many of the concretions, especially those -about organic remains. In some other cases -where there is no nucleus, as the flint in chalk, -what has taken place is that the small amounts -of silica in the lime have been dissolved, and -then around some center has constantly been -added more and more non-crystalline silica -until a mass of flint has accumulated. There -may be a considerable variety of ways to account -for different concretions, but in all cases solutions -of one mineral have come in contact with -solutions of a different kind, and precipitation -about a center has resulted.</p> -<h3><a id="species_ClayStones">Clay stones</a> -<br /><a href="#Plate_68">Pl. 68</a></h3> -<p>Of all the concretions these are -perhaps the commonest, being found -in the clays of all types and in many -regions. They are made of lime and precipitated -around some nucleus of foreign matter. The -shapes vary widely, usually discs, flattened ovals -or even rings, in most all cases however flattened. -This is indicative of the water moving -though the clay more freely in some layers than -others. Often clay stones occur so abundantly -that two or more have grown together making -fantastic shapes, sometimes resembling animals, -and all sorts of fancied but unrelated objects. -As the clay stones have grown the clay has not -been pushed aside, but has been incorporated -within the concretion; so that when a concretion -is dissolved in acid, it yields not only the lime, -<span class="pb" id="Page_251">251</span> -which is its reason for being, but also a large -amount of clay.</p> -<p>Claystones are found in clays most anywhere, -usually occurring in certain layers and being -absent from others.</p> -<h3><a id="species_LimeConcretions">Lime concretions</a></h3> -<p>These are found mostly in shales -which carry a high percentage of -clay as impurities, and are characteristic -of the older geological formations, especially -ancient sea bottoms. They are likely -to have as a nucleus some shell, fish bone, or a -leaf, which when the concretion is split, reveals a -wonderfully preserved portion of an animal or a -plant, which was buried millions of years ago. -The lime concretion is closely related to the -claystone, and is really a claystone which has -been buried so long that the surrounding matrix -has changed to a shale instead of remaining -clay.</p> -<p>One of the most famous localities for these -lime concretions is Mazon Creek, Illinois, where -thousands of these concretions have been picked -up and split to study the organic remains included. -The commonest objects found are fern -leaves, like the one on <a href="#Plate_68">Plate 68</a>. But about once -in a thousand times they inclose a spider or -insect, and once in ten thousand times the skeleton -of an amphibian, which is of especial interest, -as here have been thus found the remains of the -very earliest of the land animals. These remains -were inclosed in these concretions during -the coal age, probably 50,000,000 years -ago, and once inclosed all the hard parts have -<span class="pb" id="Page_252">252</span> -been as well preserved after that long interval, -as they were immediately after being inclosed -in the concretion. Lime concretions range from -less than an inch in diameter to several feet -through. They are not confined to shales, but -sometimes occur in sandstones, in this case also -usually having as a nucleus either a shell, or the -bone, or bones, of some animal.</p> -<p>They are likely to be found anywhere in the -limestone belt, from the Appalachian Mountains -to the Rocky Mountains, or in the Great Basin, -or on the Pacific Coast. Often they have been -mistaken for turtles and other objects. A good -many of the cases where the head or body of -animals “petrified with all the flesh” are reported, -it is one of these concretions which has a -shape sufficiently like the part described, for the -imagination to construct the rest.</p> -<h3><a id="species_Septeria">Septeria</a> -<br /><a href="#Plate_69">Pl. 69</a></h3> -<p>Septeria are lime concretions, -which, after they had formed, have -shrunk and developed a series of -cracks running through them in all sorts of directions, -and since then the cracks have been -filled with various minerals, such as calcite, -dolomite, and siderite. These make a series of -veins which intersect the concretion, in a sort of -network. Septeria are mostly of considerable -size, ranging from six inches in diameter to -several feet through. They are characteristic of -the shales of ancient sea bottoms, especially -those of Devonian age in New York, and Pennsylvania, -and those of Cretaceous age in Wyoming, -Montana and the Dakotas.</p> -<div class="pb" id="Page_253">253</div> -<h3><a id="species_FlintConcretions">Flint concretions</a></h3> -<p>The silica in limestones is often -segregated into nodular masses of -varying sizes, to make concretions of -flint. Such masses have grown in the limestone, -and, while growing, have either pushed away, or -dissolved the adjacent limestone, so that the -flint nodule is pure silica. They are especially -characteristic of the chalk beds, and of ancient -limestones which formed on the floor of the sea, -like the Helderberg Limestone of New York, -Pennsylvania, Ohio, etc. When thin sections -are cut through these flints, and examined under -the microscope, many remnants of the shells of -plants and animals are still recognizable. A -nucleus is seldom found, but in some cases there -is a fossil in the nodule about which the concretion -doubtless formed. The spicules of sponges, -shells of diatoms, and of radiolarians seem to -have contributed most of the material from -which flint concretions are formed. In addition -to the silica there are frequently inclosed in these -nodules the horny jaws of various sea worms, -and a host of spiny balls the relationships of -which are still unknown.</p> -<h3><a id="species_SandstoneConcretions">Sandstone concretions</a></h3> -<p>There are two types of sandstone -concretions, first those which are -cemented with lime, and second -those cemented with iron oxide. The concretions -bound by lime are especially characteristic -of sandstones which were laid down as river -deposits, either in the channels or on the flood -plains, and also the sandy deposits resulting -from wind deposition. In these cases the concretions -<span class="pb" id="Page_254">254</span> -will mostly be found to have formed -around some organic nucleus, most frequently -about a bone, or group of bones, of some ancient -animal. In this country they are mostly found -in the arid and semiarid sections of the West, -where the present day wind erosion exposes the -harder parts of bluffs, etc.</p> -<p>The second type of sandstone concretion is -the one in which the cement is most often -limonite, less often hematite. These concretions -are less dense than the lime ones, and in some -cases the limonite is only precipitated at a distance -from the nucleus, which has resulted in the -formation of a hollow shell, filled with loose -sand. This is especially characteristic of certain -concretions, found in a gravel or coarse sand in -the region of Middletown, Del.</p> -<h3><a id="species_Oolites">Oolites</a></h3> -<p>In large bodies of water like the -sea and some larger lakes we find -concretions which have formed, or are still -forming, about tiny grains of sand, which are -still being moved about by the waves and currents. -In such cases not only are great masses of -concretions formed but they have very clearly -marked the concentric layering, which shows -that they have increased in size, sometimes more -rapidly and sometimes more slowly. Where -great masses of such concretions have formed the -resulting rock appears like a great mass of small -eggs, whence the term oolite. The cement may -be any one of several substances, but lime, silica, -and hematite are perhaps the most common. -Here and there are found larger or smaller masses -<span class="pb" id="Page_255">255</span> -of this oolite. In some cases it would appear -that the material was precipitated by the action -of bacteria. Such for instance is probably the -origin of the Clinton iron ore, a bed of oolitic -hematite, extending from New York State all -down the Appalachian Mountains to Alabama.</p> -<h3><a id="species_Pisolite">Pisolite</a> -<br /><a href="#Plate_69">Pl. 69</a></h3> -<p>When the concretions, formed in -exactly the same manner as in the -case of oolite, are of a size bigger -than a pea, then the rock is known as pisolite.</p> -<h3 class="center"><span class="sc">Other Concretions</span></h3> -<p>Though less abundant concretion may form -from still other substances. Hematite has been -mentioned, and when concretions are made of -this material, either they have been deposited by -bacteria, or were formed as limonite and the -water of crystallization of this latter mineral -driven off.</p> -<p>Manganese concretions are found on the floor -of the ocean at maximum depths, and brought to -the surface by dredging.</p> -<h3 class="center"><span class="sc">Geodes</span></h3> -<p>Geodes are nodules, which, when broken open, -are found to be hollow and the cavity lined with -one or more minerals. They represent a special -case of minerals in a cave. There was in the -first place a cavity in the surrounding rock, -usually of sand or clay. As the water leached -through the surrounding rock, it became saturated -<span class="pb" id="Page_256">256</span> -with one or more minerals and then coming -into the cavity, deposited the minerals, either as -crystals, or as a non-crystalline mass, lining the -cavity. Thus the inside is often a beautiful -cluster of bristling crystals, or it may be simply -layer on layer of chalcedony of any color. -Before this process had gone so far as to completely -fill the cavity, erosion had dislodged -the mass, and it has been found. One usually -recognizes that it is a geode by the fact that it -is far too light to be a solid rock, and then it -may be carefully broken. They are characteristic -of certain formations; so that having accidentally -broken the first one, others can be -carefully opened to display the beauty of the -interior. The geode illustrated on <a href="#Plate_70">Plate 70</a> is -lined with quartz crystals, but near by were -found many others, some of which had chalcedony -and some jasper as a lining. Such crystallined -nodules are usually called geodes so long -as they occur in a softer matrix so that they are -easily dislodged, and until they reach a size of -three or four feet in diameter.</p> -<h3 class="center"><span class="sc">Pebbles</span></h3> -<p>When picked up either from brook beds, sea -beaches, or the open plain, there are few forms -of rock which tell a story of the past more completely -than do pebbles; and any one, who enjoys -reading a story written in form, structure and -composition, will find in pebbles one of the most -satisfying and at the same time testing exercises. -The story may be complex or simple according -<span class="pb" id="Page_257">257</span> -to what has happened to the parent rock, and -to that is added what happened since the pebble -left the ledge where it was a part of a great mass. -One must not forget to take into consideration -where the pebble was found and the character -of its associates. This sort of exercise is recommended -to all interested in rocks. It will yield -something upon first trying, and more on prolonged -study; and the fullness with which it is -done will test one’s knowledge of the meaning of -rocks as nothing else will do. As a sample of this -sort of exercise let us take the two pebbles illustrated -on <a href="#Plate_71">Plate 71</a>.</p> -<p>The upper one is a common quartz pebble -picked up in a New England brook bed. Such -pebbles are common all over the country formerly -covered by the glacial ice sheet. It is crystalline -quartz, but the individual crystals are not distinguishable, -and such quartz is typical as the -filling of veins. It therefore goes back to a time -when the rocks were fissured, probably in connection -with the folding accompanying mountain -making far to the north in Canada. Into -the fissures thus formed seeped the water which -had been leaching through the adjacent rocks, -and it was saturated with silica which it had -dissolved from those rocks. In the open fissure -the quartz was deposited as crystals, which -grew finally filling the fissure and crowding each -other so that all the faces were obliterated. The -quartz vein was complete, but it must have been -far below the surface of the ground. Time must -have passed, thousands of years of it, until, in -the weathering away of the mountain system, -<span class="pb" id="Page_258">258</span> -the many feet of overlying rock were removed -and this vein was brought to the surface. As -the quartz is harder than the adjacent rocks, the -vein soon projected as a ledge. The effect of -changes of temperature in alternately expanding -and contracting the rocks developed cracks, into -which water worked its way, and then the breaking -was hastened by the expansion which takes -place when water freezes, and in exposed regions -is so effective, because the freezing and thawing -are so often repeated. Finally an angular -fragment of quartz was dislodged and lay on the -surface, resistant to the solvent power of the -rain. In this case this happened just before the -advance of the great ice sheet. When that came -to the place where the fragment lay, it was -picked up along with all other loose material and -partly shoved in front of, but probably mostly -carried frozen in the ice, and journeyed one, two, -three hundred, perhaps a thousand miles. This -took many years for the ice moved only a few -feet a day. Finally however it came to the point -where the ice melted as fast as it advanced, and -our quartz fragment was dropped at the front -of the ice sheet along with other great masses of -till. Here there was abundant water, partly -from the melting of the ice, and partly from the -storms which must develop where there are such -contrasts in temperature, as there would be over -the ice, on one hand, and over the bare land in -front of the ice on the other hand. A torrent -picked up our fragment and started it on a second -journey, banging against other stones as it -rolled along down the stream bed, every time it -<span class="pb" id="Page_259">259</span> -struck another stone bruising the corners which -soon became rounded. Thus from time to time -during high water the quartz fragment, becoming -rounder every time it moved, journeyed down -stream, until it came to the point where the -stream emptied into a lake. Here the current -was checked and the stone dropped to the bottom -along with other larger stones to make the delta -at the mouth of the stream. There it lay as long -as the lake existed, and would be lying now, -but that in New England a tilting movement of -the land tipped the north end of the lake up and -the water all ran out. Then the stream began to -flow over its own delta and in time of freshet -tore a channel down through the old delta carrying -the pebble still further down, until it came -to the level stretch which represented the old -lake’s bottom and there it dropped the pebble -in its bed. And there it was found and picked -up to become the pebble which told the above -story of its life, and to repeat it as often as anyone -will look at it with a seeing eye.</p> -<p class="tb">The second pebble is quite a different one. -It was picked up in a gravel bank along a railroad -cut, just at the foot of Mt. Toby in Massachussetts, -and the writer has used it many times -to test his students, to see if they could read the -story which it tells.</p> -<p>It consists of two sorts of rock, the one, angular -fragments of a hornblende schist, the other, -a fine-grained granite filling all the spaces between -the fragments of schist, even in cracks -less than a quarter of an inch wide. The schist -<span class="pb" id="Page_260">260</span> -is the older rock and in its first appearance -represents a deposit of mud (clay and sand) on -the floor of the ocean, well out from the shore, -and somewhere off to the east of Mt. Toby, -perhaps ten miles, perhaps more, from the place -where it was found. This was back in early -Palæozoic times, millions of years ago.</p> -<p>This deposit was buried by further layers of -sediment on the sea bottom and cemented into a -shale. Then during a mountain making period -the region was folded, and the sediments were -altered by the combined pressure and heat, our -layer of rock becoming a hornblende schist. -After that happened considerable time must have -passed, but just how much is not indicated by -the pebble, before another period of disturbance -took place, during which this deep seated schist -was faulted, and shattered to fragments along -the line of breaking. This accounts for the -angular fragments. Then into the fissure thus -formed was pressed a molten magma, which while -liquid enough to flow and be squeezed into every -opening could not have been very hot; for not -even the corners of the schist fragments are -melted or altered, so as to appear any different -from the mass of the schist. The molten magma -cooled rather slowly, making a fine-grained -granite. This must all have taken place far -below the surface, or the magma would have -cooled into a felsite or dense lava.</p> -<p>Again a long time must have elapsed, while -the rock overlying our piece was eroded away, -so it could come to the surface. Just about the -time it did come to the surface, the Connecticut -<span class="pb" id="Page_261">261</span> -Valley was formed by a great block, 95 miles -long by fifteen to twenty miles wide, dropping -down six or eight thousand feet (probably not -all at once but by one or two hundred feet at a -time) between two north and south faults. This -took place in the Triassic Period. Of course the -streams then began to wash sand and stones of -all sizes into the hole. Our pebble was one of -these. While still an angular fragment, lying -perhaps ten miles east of the Connecticut Valley, -a stream started it moving, and as it rolled along -the brook bed, it was battered and rounded to its -present shape, and finally tumbled over a waterfall -to the bottom of the great hole, which had -been formed as described above. Here with -other stones it formed part of a coarse gravel, -coarsest near the sides of the hole, and finer -toward the middle; for the material was further -distributed in the bottom of the valley. Our -stone stayed pretty near the side and was soon -buried beneath hundreds of feet of similar material. -The leaching water dissolved enough iron -rust so that this acted on the lower layers as a -cement and bound the whole mass into a conglomerate.</p> -<p>Here for some millions of years our pebble -rested, while above it was piled sand and gravel -and a couple of sheets of lava, until the hole was -filled, and our pebble was near the bottom of the -mass. Later movements of the land raised the -whole region, fully six thousand feet, and erosion -went on for other millions of years. The conglomerate -and sandstone wore away faster than -the metamorphosed rocks on either side of the -<span class="pb" id="Page_262">262</span> -filled valley, so that a new valley, the present -Connecticut Valley, came into existence.</p> -<p>When our pebble finally came near to the -surface on the side of Mt. Toby (a mound of -conglomerate which somehow was protected -and wore down a little less rapidly than the -conglomerate on either side of it), it was just -about the time of the glacial period. The great -ice sheet went over the mountain removing all -the loose material and some more of the solid -conglomerate. This brought our pebble to the -surface, but too late to be moved by the ice. -However as soon as the ice left the Mt. Toby -region, the rains fell, and in the further weathering -of the conglomerate, the cement holding our -pebble in place was dissolved and it was freed. -At once a tiny brook started it rolling down the -side of the mountain, a brook so small that when -the pebble reached the foot of the slope it did -not have power to carry it further. Here there -gathered a fan-shaped mound of such pebbles, -known as an alluvial fan. It rested here not -over a couple of thousand years, when the Central -Vermont R. R. cut a groove through the -fan, using the material for ballast, and here the -pebble was found and brought home.</p> -<h3 class="center"><span class="sc">Meteorites</span></h3> -<p>Meteorites can hardly be called common, but -there is always a chance of finding one, and their -interest is so great, that none should escape -because unrecognized.</p> -<div class="pb" id="Page_263">263</div> -<p>Meteorites are visitors to the earth from space, -and they bring to us knowledge of the composition -of planets and solar systems, other than -our own. It is of interest to note, that while -they have brought to us some combinations of -elements which do not occur in the earth, still -they have not brought any element with which -we were not already familiar. They are popularly -known as “falling” or “shooting stars,” -though of course they are not stars, but only -small masses of matter which are entirely invisible -until they come inside our atmosphere.</p> -<p>In space there are many small (compared -with the size of the earth) chunks of matter, each -pursuing its solitary way around the sun, or -wandering through space along paths entirely -unrelated to the sun. From time to time one of -these passes near enough to the earth, so as to -be influenced by its attraction, and then comes -rushing toward it at tremendous speed, 20 to 30 -miles per second. As soon as it comes into the -atmosphere, even the very attenuated atmosphere, -a couple of hundred miles above the -surface, friction heats the surface of the meteor -until it glows, and by that light we see the so-called -shooting star, often with a trail of luminous -matter streaming out behind. Of course in -using this term “shooting star,” we understand -the meteor is no star, for they are bodies as big -as our sun, shining at distances billions of miles -away.</p> -<p>As the meteor rushes through the atmosphere -it may all burn up, no large fragment reaching -the earth’s surface. The luminous matter -<span class="pb" id="Page_264">264</span> -streaming out behind is material which has -melted and dripped off the main mass. As this -oxidizes and cools, that part which did not -become gaseous will finally fall to the earth as -fine dust. When however a meteor actually -falls to the earth, its surface is still hot, though -probably there has not been time enough for -much heat to be transmitted to the interior. -At any rate they do not show any alteration due -to this cause. On landing and sometimes before -they land meteors break into two or more pieces. -When found the surface always shows the effects -of the heat generated by the friction of passing -through the air, the surface being smoothed, and -covered with stream lines and melted out pits -and hollows, and the outer surface consisting of -a thin crust, making an appearance, which once -seen, can hardly be mistaken.</p> -<p>There are two types of meteorites, those made -wholly or largely of iron with some nickel, and -appearing like great chunks of iron, and those -which are stony and resemble a granite boulder. -In collections the first sort, <i>i.e.</i> iron meteorites, -are most abundantly represented, because most -easily recognized when found. They consist of -masses of iron and nickel with small amounts of -other elements, ranging in size from the Cape -York meteorite, which fell in northern Greenland -in 1894 and was later brought by Peary to the -American Museum, and weighs some 36 tons, -down to small grains as small as a grain of wheat. -The largest one which has fallen in the United -States was the Willamette meteorite weighing -some 15 tons, and falling 19 miles south of Portland, -<span class="pb" id="Page_265">265</span> -Oregon. These and all iron meteorites have -the iron in crystalline form which is readily seen -if the meteorite is cut, and the surface thus made -polished, then etched with acid, which is put on -and quickly washed off. Every meteorite has -its particular pattern, as illustrated on <a href="#Plate_72">Plate 72</a>, -and by these patterns can be identified. Meteorites -have a high value and are eagerly sought by -certain large institutions and collectors. Since -the crystalline structure is so characteristic of -each fall, when a new meteorite is found, it is -usually cut in two, and one part retained by the -finder or some institution; while the other part -is cut into small pieces, an inch or two on a side -and a quarter of an inch thick, but each large -enough to show the characteristic pattern. -These are distributed largely by sale to other -collectors. Thus a great meteorite collection -consists of a few large meteorites and a great -many small portions of other meteorites.</p> -<p>The second type of meteorite is the stony -meteorite. Where meteorites have been located -as they fell and recovered, the majority of them -were of this type, so that probably more than half -of the meteorites which fall are of the stony type. -However when the stony meteorite is exposed to -weathering it takes only a very short time before -the surface is eroded off and then such a meteorite -looks like any other boulder and probably -most of them fail to be recognized, and so have -been lost. Because they have so much greater -variety, they are in many ways of greater interest -than the iron type.</p> -<p>It is desirable that every one have his eye out -<span class="pb" id="Page_266">266</span> -for meteorites, and when found it is desirable that -the fact should be reported to some one of the -great institutions which collect them, such as -the National Museum in Washington, or the -American Museum in New York. Each one -should be on record even if it is desired to keep -it in a private collection.</p> -<h3 class="center"><span class="sc">Fossils</span></h3> -<p>In the sedimentary rocks one is apt to find -remains of some of the animals and plants that -lived at the time the rock was forming. While -the soft parts of animals decompose rapidly, -shells and bones are likely to be buried in the -sediments, and if the conditions have been -favorable, these remains may be preserved more -or less perfectly. All through the millions of -years that sedimentary rocks have been forming -in the sea, in lakes, on river flood plains and in -wind swept deserts, there was an abundance of -life, as much as there is today; and our knowledge -of that life is derived from these buried -fossil remains, so that fossils have a great historic -interest.</p> -<p>However as there have lived and died several -times as many different kinds of animals as live -today, the study of fossils becomes a separate -subject, which cannot be treated in this book. -Should any collector of rocks and minerals come -upon fossils, he is opening a new field, and it will -be necessary to turn to other sources for their -identification. General books on this subject -are scarce, but one or two are given in the -literature list.</p> -<div class="pb" id="Page_267">267</div> -<h3 class="center"><span class="sc">A List of the Elements, the Abbreviations Used for Them, and Their Atomic Weight, Which Is Approximately the Number of Times Heavier They Are Than Hydrogen.</span></h3> -<table class="center" summary=""> -<tr class="th"><th>Name </th><th>Oxygen = 16</th></tr> -<tr><td class="l">Aluminium, Al </td><td class="r">27</td></tr> -<tr><td class="l">Antimony, Sb </td><td class="r">122</td></tr> -<tr><td class="l">Argon, Ar </td><td class="r">40</td></tr> -<tr><td class="l">Arsenic, As </td><td class="r">75</td></tr> -<tr><td class="l">Barium, Ba </td><td class="r">137</td></tr> -<tr><td class="l">Beryllium, Be </td><td class="r">9</td></tr> -<tr><td class="l">Bismuth, Bi </td><td class="r">209</td></tr> -<tr><td class="l">Boron, B </td><td class="r">11</td></tr> -<tr><td class="l">Bromine, Br </td><td class="r">80</td></tr> -<tr><td class="l">Cadmium, Cd </td><td class="r">112</td></tr> -<tr><td class="l">Cæsium, Cs </td><td class="r">132</td></tr> -<tr><td class="l">Calcium, Ca </td><td class="r">40</td></tr> -<tr><td class="l">Carbon, C </td><td class="r">12</td></tr> -<tr><td class="l">Cerium, Ce </td><td class="r">140</td></tr> -<tr><td class="l">Chlorine, Cl </td><td class="r">35</td></tr> -<tr><td class="l">Chromium, Cr </td><td class="r">52</td></tr> -<tr><td class="l">Cobalt, Co </td><td class="r">59</td></tr> -<tr><td class="l">Columbium, Cb </td><td class="r">93</td></tr> -<tr><td class="l">Copper, Cu </td><td class="r">64</td></tr> -<tr><td class="l">Dysprosium, Dy </td><td class="r">162</td></tr> -<tr><td class="l">Erbium, Er </td><td class="r">167</td></tr> -<tr><td class="l">Europium, Eu </td><td class="r">152</td></tr> -<tr><td class="l">Fluorine, F </td><td class="r">19</td></tr> -<tr><td class="l">Gadolinium, Gd </td><td class="r">157</td></tr> -<tr><td class="l">Gallium, Ga </td><td class="r">70</td></tr> -<tr><td class="l">Germanium, Ge </td><td class="r">63</td></tr> -<tr><td class="l">Glucinum, Gl </td><td class="r">9</td></tr> -<tr><td class="l">Gold, Au </td><td class="r">197</td></tr> -<tr><td class="l">Hafnium, Hf </td><td class="r">179</td></tr> -<tr><td class="l">Helium, He </td><td class="r">4</td></tr> -<tr><td class="l">Holmium, Ho </td><td class="r">165</td></tr> -<tr><td class="l">Hydrogen, H </td><td class="r">1</td></tr> -<tr><td class="l">Indium, In </td><td class="r">115</td></tr> -<tr><td class="l">Iodine, I </td><td class="r">127</td></tr> -<tr><td class="l">Iridium, Ir </td><td class="r">193</td></tr> -<tr><td class="l">Iron, Fe </td><td class="r">56</td></tr> -<tr><td class="l">Krypton, Kr </td><td class="r">84</td></tr> -<tr><td class="l">Lanthanum, La </td><td class="r">139</td></tr> -<tr><td class="l">Lead, Pb </td><td class="r">207</td></tr> -<tr><td class="l">Lithium, Li </td><td class="r">7</td></tr> -<tr><td class="l">Lutecium, Lu </td><td class="r">175</td></tr> -<tr><td class="l">Magnesium, Mg </td><td class="r">24</td></tr> -<tr><td class="l">Manganese, Mn </td><td class="r">55</td></tr> -<tr><td class="l">Mercury, Hg </td><td class="r">201</td></tr> -<tr><td class="l">Molybdenum, Mo </td><td class="r">96</td></tr> -<tr><td class="l">Neodymium, Nd </td><td class="r">144</td></tr> -<tr><td class="l">Neon, Ne </td><td class="r">20</td></tr> -<tr><td class="l">Nickel, Ni </td><td class="r">59</td></tr> -<tr><td class="l">Nitrogen, N </td><td class="r">14</td></tr> -<tr><td class="l">Osmium, Os </td><td class="r">190</td></tr> -<tr><td class="l">Oxygen, O </td><td class="r">16</td></tr> -<tr><td class="l">Palladium, Pd </td><td class="r">107</td></tr> -<tr><td class="l">Phosphorus, P </td><td class="r">31</td></tr> -<tr><td class="l">Platinum, Pt </td><td class="r">195</td></tr> -<tr><td class="l">Potassium, K </td><td class="r">39</td></tr> -<tr><td class="l">Præseodymium, Pr </td><td class="r">141</td></tr> -<tr><td class="l">Protoactinium, Pa </td><td class="r">231</td></tr> -<tr><td class="l">Radium, Ra </td><td class="r">226</td></tr> -<tr><td class="l">Radon, Rn </td><td class="r">222</td></tr> -<tr><td class="l">Rhenium, Re </td><td class="r">186</td></tr> -<tr><td class="l">Rhodium, Rh </td><td class="r">103</td></tr> -<tr><td class="l">Rubidium, Rb </td><td class="r">85</td></tr> -<tr><td class="l">Ruthenium, Ru </td><td class="r">102</td></tr> -<tr><td class="l">Samarium, Sm </td><td class="r">150</td></tr> -<tr><td class="l">Scandium, Sc </td><td class="r">45</td></tr> -<tr><td class="l">Selenium, Se </td><td class="r">79</td></tr> -<tr><td class="l">Silicon, Si </td><td class="r">28</td></tr> -<tr><td class="l">Silver, Ag </td><td class="r">108</td></tr> -<tr><td class="l">Sodium, Na </td><td class="r">23</td></tr> -<tr><td class="l">Strontium, Sr </td><td class="r">88</td></tr> -<tr><td class="l">Sulphur, S </td><td class="r">32</td></tr> -<tr><td class="l">Tantalum, Ta </td><td class="r">181</td></tr> -<tr><td class="l">Tellurium, Te </td><td class="r">128</td></tr> -<tr><td class="l">Terbium, Tb </td><td class="r">159</td></tr> -<tr><td class="l">Thallium, Tl </td><td class="r">204</td></tr> -<tr><td class="l">Thorium, Th </td><td class="r">232</td></tr> -<tr><td class="l">Thulium, Tu </td><td class="r">169</td></tr> -<tr><td class="l">Tin, Sn </td><td class="r">119</td></tr> -<tr><td class="l">Titanium, Ti </td><td class="r">48</td></tr> -<tr><td class="l">Tungsten, W </td><td class="r">184</td></tr> -<tr><td class="l">Uranium, U </td><td class="r">238</td></tr> -<tr><td class="l">Vanadium, V </td><td class="r">51</td></tr> -<tr><td class="l">Xenon, Xe </td><td class="r">131</td></tr> -<tr><td class="l">Ytterbium, Yt </td><td class="r">173</td></tr> -<tr><td class="l">Yttrium, Y </td><td class="r">89</td></tr> -<tr><td class="l">Zinc, Zn </td><td class="r">65</td></tr> -<tr><td class="l">Zirconium, Zr </td><td class="r">91</td></tr> -</table> -<div class="pb" id="Page_268">268</div> -<h3 class="center"><span class="sc">Table of Geologic Time</span></h3> -<table class="center" summary=""> -<tr class="th"><th colspan="3"><i>Eras</i></th></tr> -<tr class="th"><th> </th><th colspan="2"><i>Periods and their Duration in Millions of Years</i> </th><th> </th><th><i>Important Physical Events</i> </th><th><i>Important Organic Events</i></th></tr> -<tr><td colspan="3" class="l">Cenozoic</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Quaternary</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Recent </td><td class="r"> </td><td class="l">Youthful land forms having high relief formed. </td><td class="l">Dominance of man.</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Pleistocene Epoch </td><td class="r">2 M.Y. </td><td class="l">Period of glaciation; four great ice advances. </td><td class="l">Heidelberg, Neanderthal, and Crô-Magnon man; extinction of large mammals.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Tertiary</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Pliocene Epoch </td><td class="r">10 M.Y. </td><td class="l">Continuing world-wide land elevation. </td><td class="l">Intermigration of North and South American mammals. Transformation of ape to man.</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Miocene Epoch </td><td class="r">18 M.Y. </td><td class="l">Cordilleras, Alps, Himalayas formed. Widespread vulcanism-basalt flows in northwestern United States. </td><td class="l">Culmination of modern types of mammals. Apes appear in Old World.</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Oligocene Epoch </td><td class="r">10 M.Y. </td><td class="l">Land dominant; seas marginal. </td><td class="l">Carnivores and ungulates develop into importance.</td></tr> -<tr><td class="l"> </td><td class="l"> </td><td class="l">Eocene Epoch </td><td class="r">20 M.Y. </td><td class="l">Extensive sedimentation; seas marginal. </td><td class="l">Dawn of the dominance of mammals. Reptiles subordinate.</td></tr> -<tr><td colspan="3" class="l">Cretaceous </td><td class="r">65 M.Y. </td><td class="l">Widespread epicontinental seas. Laramide revolution at close of period—Rocky Mountains formed. </td><td class="l">Climax and culmination of reptiles, especially dinosaurs; first flowering plants and grasses.</td></tr> -<tr class="pbtr"><td colspan="6"> -</td></tr> -<tr><td colspan="3" class="l">Mesozoic</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Jurassic </td><td class="r">38 M.Y. </td><td class="l">Continent emergent; shallow seas on western North America. </td><td class="l">Rise of birds and flying reptiles, first modern trees.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Triassic </td><td class="r">35 M.Y. </td><td class="l">Continent emergent; seas marginal. </td><td class="l">Rise of dinosaurs, cycads, and ammonites.</td></tr> -<tr><td colspan="3" class="l">Paleozoic</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Permian </td><td class="r">35 M.Y. </td><td class="l">World-wide continental uplift and mountain building. Widespread glaciation. </td><td class="l">Extinction of most Paleozoic fauna and flora. First modern insects.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Pennsylvanian </td><td class="r">48 M.Y. </td><td class="l">Continent alternately rising and sinking. </td><td class="l">Great coal-forming forests, of ferns and seed-ferns.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Mississippian </td><td class="r">35 M.Y. </td><td class="l">Low lands and widespread submergence. </td><td class="l">Culmination of crinoids, numerous sharks.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Devonian </td><td class="r">40 M.Y. </td><td class="l">Widespread submergence, local vulcanism. </td><td class="l">First known land animals, first forests.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Silurian </td><td class="r">28 M.Y. </td><td class="l">Widespread submergence, local deserts. </td><td class="l">First lung fishes and scorpions, abundant corals.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Ordovician </td><td class="r">65 M.Y. </td><td class="l">60% of North America below sea. </td><td class="l">Climax of invertebrate dominance, first vertebrate.</td></tr> -<tr><td class="l"> </td><td colspan="2" class="l">Cambrian </td><td class="r">105 M.Y. </td><td class="l">Widespread submergence. </td><td class="l">First abundant invertebrate fauna, trilobites dominant.</td></tr> -<tr><td colspan="3" class="l">Proterozoic </td><td class="r">700 ± M.Y. </td><td class="l">Long periods of granite intrusion, sedimentation, and mountain building. </td><td class="l">Bacteria and seaweeds present. Most invertebrates probably present, but remains are lacking.</td></tr> -<tr><td colspan="3" class="l">Archeozoic </td><td class="r">800 ± M.Y. </td><td class="l">World-wide intrusive igneous activity; some sediments. </td><td class="l">Blue-green algae present, primitive one-celled plants and animals probably present.</td></tr> -</table> -<div class="pb" id="Page_270">270</div> -<h2 id="c7"><span class="h2line1">BIBLIOGRAPHY</span></h2> -<h3 class="biblio">MINERALOGY</h3> -<p class="biblio"><i>Getting Acquainted with Mineralogy.</i> By G. L. English, -1936, McGraw-Hill Book Co. A beginning textbook -of mineralogy.</p> -<p class="biblio"><i>Introduction to the Study of Minerals and Rocks.</i> 3rd -Edition, by A. F. Rogers, 1937, McGraw-Hill Book -Co. Describes the commoner minerals systematically.</p> -<p class="biblio"><i>Dana’s Textbook of Mineralogy.</i> 4th Edition, revised by -W. E. Ford, 1932, John Wiley and Sons. Detailed -descriptions of minerals, their physical properties, and -their occurrence.</p> -<p class="biblio"><i>Manual of Mineralogy.</i> 15th Edition, by E. S. Dana, revised -by C. S. Hurlburt, 1941, John Wiley and Sons. -A textbook of mineralogy.</p> -<h3 class="biblio">MINERAL ECONOMICS, GEOPOLITICS</h3> -<p class="biblio"><i>World Minerals and World Peace.</i> By C. K. Leith, J. W. -Furness, and Cleona Lewis, 1943, The Brookings Institution. -Physical, economic, and political trends in -the mineral industry.</p> -<p class="biblio"><i>Minerals in World Affairs.</i> By T. S. Lovering, 1943, -Prentice-Hall.</p> -<p class="biblio"><i>Minerals Yearbook.</i> U. S. Bureau of Mines. An annual -volume presenting statistical data on the production -of the mineral resources of the United States. Reports -on individual minerals or rocks may be had -separately.</p> -<h3 class="biblio">ECONOMIC GEOLOGY</h3> -<p class="biblio"><i>Mineral Deposits.</i> 4th Edition, by W. Lindgren, 1933, -McGraw-Hill Book Co. The manner of occurrence -and origin of mineral deposits.</p> -<p class="biblio"><i>Elements of Engineering Geology.</i> 2nd Edition, by H. -Ries and T. L. Watson, 1947, John Wiley and Sons.</p> -<p class="biblio"><i>This Fascinating Oil Business.</i> By M. W. Ball, 1940, -Bobbs-Merrill Co. A simple and elementary description -of the petroleum industry.</p> -<p class="biblio"><i>Geology of Coal.</i> By O. Stutzer and A. C. Noe, 1940, -University of Chicago Press.</p> -<h3 class="biblio">GENERAL GEOLOGY</h3> -<p class="biblio"><i>Down to Earth.</i> By C. Croneis and W. C. Krumbein, -1936, University of Chicago Press. An introduction -to geology, profusely illustrated.</p> -<div class="pb" id="Page_271">271</div> -<p class="biblio"><i>Textbook of Geology Part I—Physical Geology.</i> 4th Edition, -by C. R. Longwell, A. Knopf, and R. F. Flint, -1939, John Wiley and Sons. A standard text on -geology.</p> -<p class="biblio"><i>Field Geology.</i> 4th Edition, by F. H. Lahee, 1941, -McGraw-Hill Book Co. Recognition and interpretation -of geologic structures and topographic forms as -they are observed, and methods of geologic work.</p> -<h3 class="biblio">PRECIOUS STONES</h3> -<p class="biblio"><i>A Book of Precious Stones.</i> By J. Wodiska, 1910, G. P. -Putnam’s Sons. Written for jewelers, but of general -interest.</p> -<p class="biblio"><i>The Curious Lore of Precious Stones.</i> By G. F. Kunz, -1913, Lippincott. Legends and stories of the gem -minerals.</p> -<p class="biblio"><i>The Magic of Jewels and Charms.</i> By G. F. Kunz, 1915, -Lippincott.</p> -<p class="biblio"><i>Popular Gemology.</i> By R. M. Pearl, 1948, John Wiley -and Sons. Scientific and industrial uses of gems, -current information about their locality and production.</p> -<h3 class="biblio">FOSSILS</h3> -<p class="biblio"><i>An Introduction to the Study of Fossils.</i> By H. W. -Shimer, 1933, Macmillan Co. An introductory textbook -about fossil plants and animals.</p> -<p class="biblio"><i>Invertebrate Paleontology.</i> By W. H. Twenhofel and R. -P. Shrock, 1935, McGraw-Hill Book Co.</p> -<p class="biblio"><i>Textbook of Geology Part II—Historical Geology.</i> 4th -Edition, by C. Schuchert and C. O. Dunbar, 1941, -John Wiley and Sons. The story of the development -of life through the ages.</p> -<div class="pb" id="Page_273">273</div> -<h2 id="c8"><span class="h2line1">INDEX</span></h2> -<p class="center"><a href="#index_A" class="ab">A</a> <a href="#index_B" class="ab">B</a> <a href="#index_C" class="ab">C</a> <a href="#index_D" class="ab">D</a> <a href="#index_E" class="ab">E</a> <a href="#index_F" class="ab">F</a> <a href="#index_G" class="ab">G</a> <a href="#index_H" class="ab">H</a> <a href="#index_I" class="ab">I</a> <a href="#index_J" class="ab">J</a> <a href="#index_K" class="ab">K</a> <a href="#index_L" class="ab">L</a> <a href="#index_M" class="ab">M</a> <a href="#index_N" class="ab">N</a> <a href="#index_O" class="ab">O</a> <a href="#index_P" class="ab">P</a> <a href="#index_Q" class="ab">Q</a> <a href="#index_R" class="ab">R</a> <a href="#index_S" class="ab">S</a> <a href="#index_T" class="ab">T</a> <a href="#index_U" class="ab">U</a> <a href="#index_V" class="ab">V</a> <a href="#index_W" class="ab">W</a> <a href="#index_X" class="ab">X</a> <span class="ab">Y</span> <a href="#index_Z" class="ab">Z</a></p> -<dl class="index"> -<dt class="center b" id="index_A">A</dt> -<dt>Actinolite, <a href="#Page_120">120</a></dt> -<dt>Adobe, <a href="#Page_210">210</a></dt> -<dt>Agate, <a href="#Page_107">107</a></dt> -<dt>Agate, moss, <a href="#Page_73">73</a>, <a href="#Page_108">108</a></dt> -<dt>Alabaster, <a href="#Page_152">152</a></dt> -<dt>Albertite, <a href="#Page_229">229</a></dt> -<dt>Albite, <a href="#Page_110">110</a>, <a href="#Page_113">113</a>, <a href="#Page_115">115</a></dt> -<dt>Almandine, <a href="#Page_97">97</a></dt> -<dt>Almandite, <a href="#Page_122">122</a>, <a href="#Page_123">123</a></dt> -<dt>Aluminum bronze, <a href="#Page_74">74</a></dt> -<dt>Aluminum group, <a href="#Page_73">73</a></dt> -<dt>Amazon stone, <a href="#Page_114">114</a></dt> -<dt>Amber, <a href="#Page_223">223</a></dt> -<dt>Amethyst, <a href="#Page_104">104</a></dt> -<dt>Amethyst, Oriental, <a href="#Page_75">75</a></dt> -<dt>Amianthus, <a href="#Page_120">120</a></dt> -<dt>Amphibole group, <a href="#Page_119">119</a></dt> -<dt>Amygdoloid, <a href="#Page_194">194</a></dt> -<dt>Amygdoloidal, <a href="#Page_176">176</a></dt> -<dt>Analcite, <a href="#Page_141">141</a></dt> -<dt>Andesite, <a href="#Page_113">113</a>, <a href="#Page_187">187</a></dt> -<dt>Andradite, <a href="#Page_122">122</a>, <a href="#Page_124">124</a></dt> -<dt>Anglesite, <a href="#Page_62">62</a></dt> -<dt>Anhydrite, <a href="#Page_149">149</a></dt> -<dt>Anorthite, <a href="#Page_110">110</a>, <a href="#Page_113">113</a></dt> -<dt>Anorthosite, <a href="#Page_183">183</a></dt> -<dt>Anthracite, <a href="#Page_218">218</a>, <a href="#Page_222">222</a></dt> -<dt>Antimony, <a href="#Page_81">81</a></dt> -<dt>Antimony, gray, <a href="#Page_81">81</a></dt> -<dt>Apatite, <a href="#Page_160">160</a></dt> -<dt>Aquamarine, <a href="#Page_125">125</a></dt> -<dt>Aragonite, <a href="#Page_147">147</a></dt> -<dt>Argentite, <a href="#Page_35">35</a></dt> -<dt>Argillite, <a href="#Page_242">242</a></dt> -<dt>Arkose, <a href="#Page_206">206</a></dt> -<dt>Arsenic group, <a href="#Page_78">78</a></dt> -<dt>Arsenopyrite, <a href="#Page_79">79</a></dt> -<dt>Asbestos, <a href="#Page_120">120</a>, <a href="#Page_140">140</a></dt> -<dt>Augite, <a href="#Page_118">118</a></dt> -<dt>Aventurine, <a href="#Page_104">104</a></dt> -<dt>Azurite, <a href="#Page_46">46</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_B">B</dt> -<dt>Barite, <a href="#Page_154">154</a></dt> -<dt>Barium group, <a href="#Page_154">154</a></dt> -<dt>Basalt, <a href="#Page_188">188</a></dt> -<dt>Batholith, <a href="#Page_174">174</a></dt> -<dt>Bauxite, <a href="#Page_77">77</a></dt> -<dt>Beryl, <a href="#Page_125">125</a></dt> -<dt>Beryl, golden, <a href="#Page_125">125</a></dt> -<dt>Beryllium, <a href="#Page_125">125</a></dt> -<dt>Bibliography, <a href="#Page_270">270</a></dt> -<dt>Biotite, <a href="#Page_129">129</a>, <a href="#Page_130">130</a></dt> -<dt>Bitumen, <a href="#Page_228">228</a></dt> -<dt>Black jack, <a href="#Page_65">65</a></dt> -<dt>Bloodstone, <a href="#Page_106">106</a></dt> -<dt>Bog lime, <a href="#Page_213">213</a></dt> -<dt>Bombs, <a href="#Page_191">191</a></dt> -<dt>Boracite, <a href="#Page_164">164</a></dt> -<dt>Borax, <a href="#Page_165">165</a></dt> -<dt>Bornite, <a href="#Page_41">41</a></dt> -<dt>Brass, <a href="#Page_64">64</a></dt> -<dt>Breccia, <a href="#Page_191">191</a>, <a href="#Page_198">198</a></dt> -<dt>Brittania metal, <a href="#Page_81">81</a></dt> -<dt>Bronze, <a href="#Page_38">38</a></dt> -<dt>Bronze Age, <a href="#Page_38">38</a></dt> -<dt>Bronzite, <a href="#Page_118">118</a></dt> -<dt>Bytownite, <a href="#Page_113">113</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_C">C</dt> -<dt>Calamine, <a href="#Page_68">68</a></dt> -<dt>Calaverite, <a href="#Page_30">30</a></dt> -<dt>Calcite, <a href="#Page_144">144</a></dt> -<dt>Calcium, <a href="#Page_143">143</a></dt> -<dt>Carbon, <a href="#Page_156">156</a></dt> -<dt>Carbonite, <a href="#Page_222">222</a></dt> -<dt>Carbuncle, <a href="#Page_124">124</a></dt> -<dt>Carnelian, <a href="#Page_106">106</a></dt> -<dt>Carnotite, <a href="#Page_90">90</a></dt> -<dt>Cassiterite, <a href="#Page_93">93</a></dt> -<dt>Cat’s eye, <a href="#Page_104">104</a></dt> -<dt>Celestite, <a href="#Page_153">153</a></dt> -<dt>Cerargyrite, <a href="#Page_37">37</a></dt> -<dt>Cerrusite, <a href="#Page_61">61</a></dt> -<dt>Ceylonite, <a href="#Page_97">97</a></dt> -<dt class="pb" id="Page_274">274</dt> -<dt>Chalcedony, <a href="#Page_104">104</a>, <a href="#Page_106">106</a></dt> -<dt>Chalcocite, <a href="#Page_42">42</a></dt> -<dt>Chalcopyrite, <a href="#Page_40">40</a></dt> -<dt>Chalcotrichite, <a href="#Page_45">45</a></dt> -<dt>Chalk, <a href="#Page_213">213</a></dt> -<dt>Chert, <a href="#Page_107">107</a></dt> -<dt>Chlorite, <a href="#Page_140">140</a></dt> -<dt>Chlorospinel, <a href="#Page_98">98</a></dt> -<dt>Chromite, <a href="#Page_87">87</a></dt> -<dt>Chromium, <a href="#Page_86">86</a></dt> -<dt>Chrysocola, <a href="#Page_47">47</a></dt> -<dt>Chrysolite, <a href="#Page_134">134</a>, <a href="#Page_140">140</a></dt> -<dt>Chrysoprase, <a href="#Page_106">106</a></dt> -<dt>Cinnabar, <a href="#Page_91">91</a></dt> -<dt>Cinnamon stone, <a href="#Page_123">123</a></dt> -<dt>Citrine, <a href="#Page_103">103</a></dt> -<dt>Clay, <a href="#Page_207">207</a></dt> -<dt>Clay, ball, <a href="#Page_208">208</a></dt> -<dt>Clay, brick, <a href="#Page_209">209</a></dt> -<dt>Clay, china, <a href="#Page_208">208</a></dt> -<dt>Clay, fire, <a href="#Page_208">208</a></dt> -<dt>Clay, paving brick, <a href="#Page_209">209</a></dt> -<dt>Clay, sewer-pipe, <a href="#Page_209">209</a></dt> -<dt>Clay, slip, <a href="#Page_209">209</a></dt> -<dt>Clay, stoneware, <a href="#Page_209">209</a></dt> -<dt>Clay stones, <a href="#Page_250">250</a></dt> -<dt>Cleavage, <a href="#Page_21">21</a></dt> -<dt>Cleavage, slaty, <a href="#Page_234">234</a></dt> -<dt>Coal, <a href="#Page_217">217</a></dt> -<dt>Coal, bituminous, <a href="#Page_212">212</a>, <a href="#Page_220">220</a></dt> -<dt>Coal, cannel, <a href="#Page_221">221</a></dt> -<dt>Coal, hard, <a href="#Page_222">222</a></dt> -<dt>Coal, soft, <a href="#Page_220">220</a></dt> -<dt>Cobalt, <a href="#Page_84">84</a></dt> -<dt>Cobalt bloom, <a href="#Page_85">85</a></dt> -<dt>Cobalt glance, <a href="#Page_85">85</a></dt> -<dt>Cobalt gray ore, <a href="#Page_85">85</a></dt> -<dt>Cobaltite, <a href="#Page_83">83</a></dt> -<dt>Coke, <a href="#Page_220">220</a></dt> -<dt>Colemanite, <a href="#Page_165">165</a></dt> -<dt>Collecting, <a href="#Page_5">5</a>, <a href="#Page_7">7</a></dt> -<dt>Color, <a href="#Page_23">23</a></dt> -<dt>Concretions, <a href="#Page_248">248</a></dt> -<dt>Concretions, flint, <a href="#Page_253">253</a></dt> -<dt>Concretions, lime, <a href="#Page_251">251</a></dt> -<dt>Concretions, other, <a href="#Page_255">255</a></dt> -<dt>Concretions, sandstone, <a href="#Page_253">253</a></dt> -<dt>Conglomerate, <a href="#Page_202">202</a></dt> -<dt>Copper, <a href="#Page_37">37</a>, <a href="#Page_39">39</a></dt> -<dt>Copper, blushing, <a href="#Page_42">42</a></dt> -<dt>Copper, glance, <a href="#Page_42">42</a></dt> -<dt>Copper, grey, <a href="#Page_43">43</a></dt> -<dt>Copper, peacock, <a href="#Page_42">42</a></dt> -<dt>Copper, plush, <a href="#Page_45">45</a></dt> -<dt>Copper, purple, <a href="#Page_41">41</a></dt> -<dt>Copper, red, <a href="#Page_44">44</a></dt> -<dt>Copper, variegated, <a href="#Page_42">42</a></dt> -<dt>Copper, yellow, <a href="#Page_40">40</a></dt> -<dt>Coquina, <a href="#Page_213">213</a></dt> -<dt>Coral, <a href="#Page_146">146</a></dt> -<dt>Coral rock, <a href="#Page_214">214</a></dt> -<dt>Corundum, <a href="#Page_75">75</a></dt> -<dt>Crude oil, <a href="#Page_227">227</a></dt> -<dt>Cryolite, <a href="#Page_78">78</a></dt> -<dt>Crystal balls, <a href="#Page_101">101</a></dt> -<dt>Crystal formation, <a href="#Page_14">14</a></dt> -<dt>Crystal rock, <a href="#Page_103">103</a></dt> -<dt>Crystal structure, <a href="#Page_11">11</a></dt> -<dt>Crystal systems, <a href="#Page_13">13</a>-18</dt> -<dt>Cuprite, <a href="#Page_44">44</a></dt> -<dt>Cyanite, <a href="#Page_128">128</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_D">D</dt> -<dt>Dacite, <a href="#Page_187">187</a></dt> -<dt>Dense, <a href="#Page_176">176</a></dt> -<dt>Diamond, <a href="#Page_157">157</a></dt> -<dt>Diamonds, Matura, <a href="#Page_127">127</a></dt> -<dt>Diamonds, slave’s, <a href="#Page_133">133</a></dt> -<dt>Diatoms, <a href="#Page_231">231</a></dt> -<dt>Dikes, <a href="#Page_174">174</a></dt> -<dt>Diorite, <a href="#Page_182">182</a></dt> -<dt>Dog-tooth spar, <a href="#Page_145">145</a></dt> -<dt>Dolomite, <a href="#Page_99">99</a></dt> -<dt>Dry bone, <a href="#Page_68">68</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_E">E</dt> -<dt>Earth, diatomaceous, <a href="#Page_23">23</a></dt> -<dt>Elements, listed, <a href="#Page_267">267</a></dt> -<dt>Emerald, <a href="#Page_125">125</a></dt> -<dt>Emerald, Oriental, <a href="#Page_75">75</a></dt> -<dt>Emery, <a href="#Page_76">76</a></dt> -<dt>Enstatite, <a href="#Page_117">117</a></dt> -<dt>Epidote, <a href="#Page_134">134</a></dt> -<dt>Equipment, <a href="#Page_7">7</a></dt> -<dt>Erubescite, <a href="#Page_42">42</a></dt> -<dt>Extrusive, <a href="#Page_173">173</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_F">F</dt> -<dt>Feldspar, <a href="#Page_110">110</a></dt> -<dt>Feldspar, alkalic, <a href="#Page_111">111</a></dt> -<dt>Felsite, <a href="#Page_186">186</a></dt> -<dt>Felsitic, <a href="#Page_176">176</a></dt> -<dt>Ferromanganese, <a href="#Page_70">70</a></dt> -<dt>Flagstone, <a href="#Page_207">207</a></dt> -<dt>Flint, <a href="#Page_106">106</a></dt> -<dt class="pb" id="Page_275">275</dt> -<dt>Fluorine, <a href="#Page_162">162</a></dt> -<dt>Fluorite, <a href="#Page_162">162</a></dt> -<dt>Fossils, <a href="#Page_266">266</a></dt> -<dt>Fragmental, <a href="#Page_176">176</a></dt> -<dt>Franklinite, <a href="#Page_69">69</a></dt> -<dt>Freestone, <a href="#Page_207">207</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_G">G</dt> -<dt>Gabbro, <a href="#Page_183">183</a></dt> -<dt>Galena, <a href="#Page_60">60</a></dt> -<dt>Garnet group, <a href="#Page_121">121</a></dt> -<dt>Garnet, Sirian, <a href="#Page_123">123</a></dt> -<dt>Geodes, <a href="#Page_255">255</a></dt> -<dt>German silver, <a href="#Page_82">82</a></dt> -<dt>Gilsonite, <a href="#Page_229">229</a></dt> -<dt>Glassy, <a href="#Page_176">176</a></dt> -<dt>Glucinum, <a href="#Page_125">125</a></dt> -<dt>Gneiss, <a href="#Page_237">237</a></dt> -<dt>Goethite, <a href="#Page_51">51</a>, <a href="#Page_52">52</a></dt> -<dt>Gold, <a href="#Page_31">31</a></dt> -<dt>Gold foil, <a href="#Page_64">64</a></dt> -<dt>Gold group, <a href="#Page_29">29</a></dt> -<dt>Gossan, <a href="#Page_50">50</a></dt> -<dt>Granite, <a href="#Page_178">178</a></dt> -<dt>Granite, graphic, <a href="#Page_179">179</a></dt> -<dt>Granitoid, <a href="#Page_176">176</a></dt> -<dt>Graphite, <a href="#Page_156">156</a>, <a href="#Page_219">219</a></dt> -<dt>Gravel, <a href="#Page_201">201</a></dt> -<dt>Graywacke, <a href="#Page_206">206</a></dt> -<dt>Grit, <a href="#Page_206">206</a></dt> -<dt>Grossularite, <a href="#Page_122">122</a>, <a href="#Page_123">123</a></dt> -<dt>Guano, <a href="#Page_230">230</a></dt> -<dt>Gumbo, <a href="#Page_210">210</a></dt> -<dt>Gypsum, <a href="#Page_150">150</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_H">H</dt> -<dt>Halite, <a href="#Page_163">163</a></dt> -<dt>Hardness, <a href="#Page_20">20</a></dt> -<dt>Hardpan, <a href="#Page_216">216</a></dt> -<dt>Heavy spar, <a href="#Page_154">154</a></dt> -<dt>Heliotrope, <a href="#Page_106">106</a></dt> -<dt>Hematite, <a href="#Page_53">53</a></dt> -<dt>Hemihedral forms, <a href="#Page_19">19</a></dt> -<dt>Hercynite, <a href="#Page_98">98</a></dt> -<dt>Hexagonal system, <a href="#Page_18">18</a></dt> -<dt>Hornblende, <a href="#Page_121">121</a></dt> -<dt>Hornstone, <a href="#Page_107">107</a></dt> -<dt>Hyacinth, <a href="#Page_127">127</a></dt> -<dt>Hypersthene, <a href="#Page_118">118</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_I">I</dt> -<dt>Ice, <a href="#Page_167">167</a></dt> -<dt>Iceland spar, <a href="#Page_145">145</a></dt> -<dt>Ice stone, <a href="#Page_78">78</a></dt> -<dt>Ilmenite, <a href="#Page_94">94</a></dt> -<dt>Intrusive, <a href="#Page_174">174</a></dt> -<dt>Iron, <a href="#Page_47">47</a></dt> -<dt>Iron, bog, <a href="#Page_50">50</a></dt> -<dt>Iron, chromic, <a href="#Page_87">87</a></dt> -<dt>Iron, magnetic, <a href="#Page_54">54</a></dt> -<dt>Iron pyrites, <a href="#Page_56">56</a></dt> -<dt>Iron, spathic, <a href="#Page_55">55</a></dt> -<dt>Iron, specular, <a href="#Page_53">53</a></dt> -<dt>Isometric system, <a href="#Page_13">13</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_J">J</dt> -<dt>Jacinth, <a href="#Page_127">127</a></dt> -<dt>Jargons, <a href="#Page_127">127</a></dt> -<dt>Jargoons, <a href="#Page_127">127</a></dt> -<dt>Jasper, <a href="#Page_106">106</a></dt> -<dt>Jet, <a href="#Page_222">222</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_K">K</dt> -<dt>Kaolin, <a href="#Page_137">137</a>, <a href="#Page_208">208</a></dt> -<dt>Kaolinite, <a href="#Page_137">137</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_L">L</dt> -<dt>Labels, <a href="#Page_5">5</a></dt> -<dt>Labradorite, <a href="#Page_113">113</a>, <a href="#Page_116">116</a></dt> -<dt>Laccolith, <a href="#Page_174">174</a></dt> -<dt>Lapilli, <a href="#Page_191">191</a></dt> -<dt>Lava, <a href="#Page_173">173</a></dt> -<dt>Lead, <a href="#Page_59">59</a></dt> -<dt>Lead glance, <a href="#Page_60">60</a></dt> -<dt>Lead, green ore, <a href="#Page_63">63</a></dt> -<dt>Lead, white ore, <a href="#Page_61">61</a></dt> -<dt>Lepidolite, <a href="#Page_129">129</a>, <a href="#Page_130">130</a></dt> -<dt>Lignite, <a href="#Page_218">218</a>, <a href="#Page_219">219</a></dt> -<dt>Limestone, <a href="#Page_212">212</a></dt> -<dt>Limestone, encrinal, <a href="#Page_214">214</a></dt> -<dt>Limestone, hydraulic, <a href="#Page_214">214</a></dt> -<dt>Limestone, lithographic, <a href="#Page_214">214</a></dt> -<dt>Limonite, <a href="#Page_49">49</a>, <a href="#Page_51">51</a></dt> -<dt>Loess, <a href="#Page_210">210</a></dt> -<dt>Luster, <a href="#Page_23">23</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_M">M</dt> -<dt>Magma, <a href="#Page_173">173</a></dt> -<dt>Magnesite, <a href="#Page_98">98</a></dt> -<dt>Magnesium group, <a href="#Page_96">96</a></dt> -<dt>Magnetite, <a href="#Page_54">54</a></dt> -<dt>Malachite, <a href="#Page_45">45</a></dt> -<dt>Malanite, <a href="#Page_124">124</a></dt> -<dt>Malta, <a href="#Page_229">229</a></dt> -<dt>Manganese group, <a href="#Page_70">70</a></dt> -<dt>Manganite, <a href="#Page_72">72</a></dt> -<dt>Marble, <a href="#Page_243">243</a></dt> -<dt>Marble, Suisun, <a href="#Page_146">146</a></dt> -<dt class="pb" id="Page_276">276</dt> -<dt>Marcasite, <a href="#Page_57">57</a></dt> -<dt>Marl, <a href="#Page_211">211</a></dt> -<dt>Mercury, <a href="#Page_90">90</a></dt> -<dt>Meteorites, <a href="#Page_262">262</a></dt> -<dt>Mica group, <a href="#Page_128">128</a></dt> -<dt>Microcline, <a href="#Page_113">113</a>, <a href="#Page_114">114</a></dt> -<dt>Millerite, <a href="#Page_83">83</a></dt> -<dt>Mineral tables, <a href="#Page_25">25</a></dt> -<dt>Minerals, defined, <a href="#Page_10">10</a></dt> -<dt>Molybdenite, <a href="#Page_81">81</a></dt> -<dt>Molybdenum, <a href="#Page_80">80</a></dt> -<dt>Monoclinic system, <a href="#Page_17">17</a></dt> -<dt>Monzonite, <a href="#Page_181">181</a></dt> -<dt>Morion, <a href="#Page_103">103</a></dt> -<dt>Mother-of-pearl, <a href="#Page_148">148</a></dt> -<dt>Muscovite, <a href="#Page_129">129</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_N">N</dt> -<dt>Natrolite, <a href="#Page_142">142</a></dt> -<dt>Natural gas, <a href="#Page_227">227</a></dt> -<dt>Needle iron stone, <a href="#Page_52">52</a></dt> -<dt>Niccolite, <a href="#Page_83">83</a></dt> -<dt>Nickel, copper, <a href="#Page_83">83</a></dt> -<dt>Nickel group, <a href="#Page_82">82</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_O">O</dt> -<dt>Obsidian, <a href="#Page_191">191</a></dt> -<dt>Ochre red, <a href="#Page_54">54</a></dt> -<dt>Ochre yellow, <a href="#Page_49">49</a></dt> -<dt>Oligoclase, <a href="#Page_113">113</a>, <a href="#Page_115">115</a></dt> -<dt>Olivine, <a href="#Page_134">134</a></dt> -<dt>Olivine-gabbro, <a href="#Page_183">183</a></dt> -<dt>Onyx, <a href="#Page_108">108</a></dt> -<dt>Onyx, Californian, <a href="#Page_146">146</a></dt> -<dt>Onyx marble, <a href="#Page_215">215</a></dt> -<dt>Onyx, Mexican, <a href="#Page_146">146</a></dt> -<dt>Oolites, <a href="#Page_254">254</a></dt> -<dt>Opal, <a href="#Page_108">108</a></dt> -<dt>Opal-agate, <a href="#Page_109">109</a></dt> -<dt>Opal, common, <a href="#Page_109">109</a></dt> -<dt>Opal, fire, <a href="#Page_109">109</a></dt> -<dt>Opal, precious, <a href="#Page_109">109</a></dt> -<dt>Ophicalcite, <a href="#Page_246">246</a></dt> -<dt>Ophiolite, <a href="#Page_246">246</a></dt> -<dt>Orpiment, <a href="#Page_80">80</a></dt> -<dt>Orthoclase, <a href="#Page_110">110</a>, <a href="#Page_113">113</a></dt> -<dt>Orthorhombic system, <a href="#Page_16">16</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_P">P</dt> -<dt>Paste, <a href="#Page_103">103</a></dt> -<dt>Pearls, <a href="#Page_148">148</a></dt> -<dt>Pearlstone, <a href="#Page_193">193</a></dt> -<dt>Peat, <a href="#Page_218">218</a>, <a href="#Page_219">219</a></dt> -<dt>Pebbles, <a href="#Page_256">256</a></dt> -<dt>Pegmatite, <a href="#Page_179">179</a></dt> -<dt>Peridot, <a href="#Page_134">134</a></dt> -<dt>Peridotite, <a href="#Page_184">184</a></dt> -<dt>Perlite, <a href="#Page_193">193</a></dt> -<dt>Petroleum series, <a href="#Page_224">224</a>, <a href="#Page_227">227</a></dt> -<dt>Pewter, <a href="#Page_60">60</a></dt> -<dt>Phenocrysts, <a href="#Page_189">189</a></dt> -<dt>Phlogopite, <a href="#Page_129">129</a>, <a href="#Page_131">131</a></dt> -<dt>Phosphate, <a href="#Page_160">160</a>, <a href="#Page_230">230</a></dt> -<dt>Phosphorus, <a href="#Page_159">159</a></dt> -<dt>Phyllite, <a href="#Page_242">242</a></dt> -<dt>Picotite, <a href="#Page_97">97</a></dt> -<dt>Pisolite, <a href="#Page_255">255</a></dt> -<dt>Pitchstone, <a href="#Page_193">193</a></dt> -<dt>Plagioclase, <a href="#Page_111">111</a></dt> -<dt>Plasma, <a href="#Page_106">106</a></dt> -<dt>Platinum, <a href="#Page_95">95</a></dt> -<dt>Plumbago, <a href="#Page_156">156</a></dt> -<dt>Porous, <a href="#Page_176">176</a></dt> -<dt>Porphyritic, <a href="#Page_176">176</a></dt> -<dt>Porphyry, <a href="#Page_189">189</a></dt> -<dt>Prase, <a href="#Page_104">104</a></dt> -<dt>Prousite, <a href="#Page_36">36</a></dt> -<dt>Psilomelane, <a href="#Page_72">72</a></dt> -<dt>Pumice, <a href="#Page_193">193</a></dt> -<dt>Pyrargyrite, <a href="#Page_35">35</a></dt> -<dt>Pyrite, <a href="#Page_56">56</a></dt> -<dt>Pyrite, capillary, <a href="#Page_83">83</a></dt> -<dt>Pyrite, magnetic, <a href="#Page_58">58</a></dt> -<dt>Pyrite, white, <a href="#Page_57">57</a></dt> -<dt>Pyritohedron, <a href="#Page_56">56</a>, <a href="#Page_318">318</a></dt> -<dt>Pyrolusite, <a href="#Page_71">71</a></dt> -<dt>Pyromorphite, <a href="#Page_63">63</a></dt> -<dt>Pyrope, <a href="#Page_122">122</a>, <a href="#Page_123">123</a></dt> -<dt>Pyroxene group, <a href="#Page_116">116</a></dt> -<dt>Pyroxenite, <a href="#Page_185">185</a></dt> -<dt>Pyrrhotite, <a href="#Page_58">58</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_Q">Q</dt> -<dt>Quartz, <a href="#Page_100">100</a></dt> -<dt>Quartz-diorite, <a href="#Page_181">181</a></dt> -<dt>Quartz, milky, <a href="#Page_103">103</a></dt> -<dt>Quartz, rose, <a href="#Page_104">104</a></dt> -<dt>Quartz, smoky, <a href="#Page_103">103</a></dt> -<dt>Quartzite, <a href="#Page_239">239</a></dt> -<dt>Quicksands, <a href="#Page_204">204</a></dt> -<dt>Quicksilver, <a href="#Page_90">90</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_R">R</dt> -<dt>Radium, <a href="#Page_89">89</a></dt> -<dt>Realgar, <a href="#Page_80">80</a></dt> -<dt>Rhinestones, <a href="#Page_101">101</a></dt> -<dt>Rhodochrosite, <a href="#Page_73">73</a></dt> -<dt class="pb" id="Page_277">277</dt> -<dt>Rhyolite 185</dt> -<dt>Rock, phosphate, <a href="#Page_230">230</a></dt> -<dt>Rocks, <a href="#Page_170">170</a></dt> -<dt>Rocks, defined, <a href="#Page_10">10</a></dt> -<dt>Rocks, igneous, <a href="#Page_172">172</a></dt> -<dt>Rocks, igneous, classified, <a href="#Page_177">177</a></dt> -<dt>Rocks, metamorphic, <a href="#Page_232">232</a></dt> -<dt>Rocks, metamorphic, classified, <a href="#Page_236">236</a></dt> -<dt>Rocks, sedimentary, <a href="#Page_194">194</a></dt> -<dt>Rocks, sedimentary, classified, <a href="#Page_196">196</a></dt> -<dt>Rubicelle, <a href="#Page_97">97</a></dt> -<dt>Ruby, <a href="#Page_75">75</a></dt> -<dt>Ruby, Balas, <a href="#Page_97">97</a></dt> -<dt>Ruby mica, <a href="#Page_52">52</a></dt> -<dt>Rutile, <a href="#Page_94">94</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_S">S</dt> -<dt>Salt, <a href="#Page_163">163</a></dt> -<dt>Sand, <a href="#Page_202">202</a></dt> -<dt>Sandstone, <a href="#Page_205">205</a></dt> -<dt>Sapphire, <a href="#Page_75">75</a></dt> -<dt>Sapphire, Oriental white, <a href="#Page_75">75</a></dt> -<dt>Sardonyx, <a href="#Page_108">108</a></dt> -<dt>Satin spar, <a href="#Page_146">146</a></dt> -<dt>Schist, <a href="#Page_240">240</a></dt> -<dt>Schistosity, <a href="#Page_234">234</a></dt> -<dt>Scoria, <a href="#Page_192">192</a>, <a href="#Page_193">193</a></dt> -<dt>Septeria, <a href="#Page_252">252</a></dt> -<dt>Sericite, <a href="#Page_130">130</a></dt> -<dt>Serpentine, <a href="#Page_139">139</a>, <a href="#Page_245">245</a></dt> -<dt>Shale, <a href="#Page_210">210</a></dt> -<dt>Shale, oil-bearing, <a href="#Page_225">225</a></dt> -<dt>Sheet, <a href="#Page_173">173</a></dt> -<dt>Siderite, <a href="#Page_55">55</a></dt> -<dt>Silica, <a href="#Page_99">99</a></dt> -<dt>Silicates, <a href="#Page_99">99</a></dt> -<dt>Silicon, <a href="#Page_99">99</a></dt> -<dt>Sill, <a href="#Page_174">174</a></dt> -<dt>Sillimanite, <a href="#Page_128">128</a></dt> -<dt>Silver, <a href="#Page_34">34</a></dt> -<dt>Silver, dark red, <a href="#Page_35">35</a></dt> -<dt>Silver, German, <a href="#Page_65">65</a></dt> -<dt>Silver glance, <a href="#Page_35">35</a></dt> -<dt>Silver group, <a href="#Page_32">32</a></dt> -<dt>Silver, horn, <a href="#Page_37">37</a></dt> -<dt>Silver, light red, <a href="#Page_36">36</a></dt> -<dt>Silver, ruby, <a href="#Page_35">35</a></dt> -<dt>Sinter, <a href="#Page_110">110</a></dt> -<dt>Slate, <a href="#Page_241">241</a></dt> -<dt>Smalt, <a href="#Page_84">84</a></dt> -<dt>Smaltite, <a href="#Page_85">85</a></dt> -<dt>Smithsonite, <a href="#Page_68">68</a></dt> -<dt>Soapstone, <a href="#Page_244">244</a></dt> -<dt>Sodalite, <a href="#Page_126">126</a></dt> -<dt>Soil, <a href="#Page_198">198</a></dt> -<dt>Solder, <a href="#Page_60">60</a></dt> -<dt>Specific gravity, <a href="#Page_22">22</a></dt> -<dt>Speigeleisen, <a href="#Page_70">70</a></dt> -<dt>Spelter, <a href="#Page_64">64</a></dt> -<dt>Spessartite, <a href="#Page_122">122</a>, <a href="#Page_123">123</a></dt> -<dt>Sphalerite, <a href="#Page_65">65</a></dt> -<dt>Spinel, <a href="#Page_97">97</a></dt> -<dt>Spinel-ruby, <a href="#Page_97">97</a></dt> -<dt>Stalactites, <a href="#Page_146">146</a></dt> -<dt>Stalagmites, <a href="#Page_146">146</a></dt> -<dt>Staurolite, <a href="#Page_133">133</a></dt> -<dt>Steatite, <a href="#Page_244">244</a></dt> -<dt>Stellite, <a href="#Page_84">84</a>, <a href="#Page_88">88</a></dt> -<dt>Stibnite, <a href="#Page_81">81</a></dt> -<dt>Stilbite, <a href="#Page_143">143</a></dt> -<dt>Stock, <a href="#Page_174">174</a></dt> -<dt>Streak, <a href="#Page_23">23</a></dt> -<dt>Strontianite, <a href="#Page_152">152</a></dt> -<dt>Strontium group, <a href="#Page_152">152</a></dt> -<dt>Sulphur, <a href="#Page_166">166</a></dt> -<dt>Syenite, <a href="#Page_180">180</a></dt> -<dt>Sylvanite, <a href="#Page_30">30</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_T">T</dt> -<dt>Talc, <a href="#Page_138">138</a></dt> -<dt>Talus, <a href="#Page_197">197</a></dt> -<dt>Tetragonal system, <a href="#Page_15">15</a></dt> -<dt>Tetrahedrite, <a href="#Page_43">43</a></dt> -<dt>Tile ore, <a href="#Page_45">45</a></dt> -<dt>Till, <a href="#Page_215">215</a></dt> -<dt>Tillite, <a href="#Page_217">217</a></dt> -<dt>Time chart, <a href="#Page_268">268</a></dt> -<dt>Tin, <a href="#Page_92">92</a></dt> -<dt>Tin stone, <a href="#Page_93">93</a></dt> -<dt>Titanium, <a href="#Page_93">93</a></dt> -<dt>Tonalite, <a href="#Page_181">181</a></dt> -<dt>Topaz, <a href="#Page_131">131</a></dt> -<dt>Topaz, false, <a href="#Page_103">103</a></dt> -<dt>Topaz, Oriental, <a href="#Page_75">75</a></dt> -<dt>Topaz, Saxon, <a href="#Page_132">132</a></dt> -<dt>Topaz, Scotch, <a href="#Page_132">132</a></dt> -<dt>Topaz, smoky, <a href="#Page_132">132</a></dt> -<dt>Topaz, Spanish, <a href="#Page_132">132</a></dt> -<dt>Tourmaline, <a href="#Page_135">135</a></dt> -<dt>Trachite, <a href="#Page_186">186</a></dt> -<dt>Trap, <a href="#Page_188">188</a></dt> -<dt>Travertine, <a href="#Page_146">146</a>, <a href="#Page_215">215</a></dt> -<dt class="pb" id="Page_278">278</dt> -<dt>Tremolite, <a href="#Page_120">120</a></dt> -<dt>Triclinic system, <a href="#Page_18">18</a></dt> -<dt>Tripolite, <a href="#Page_110">110</a></dt> -<dt>Tufa, calcareous, <a href="#Page_147">147</a></dt> -<dt>Tuff, <a href="#Page_190">190</a></dt> -<dt>Tungsten, <a href="#Page_87">87</a></dt> -<dt>Turgite, <a href="#Page_51">51</a></dt> -<dt>Turquois, <a href="#Page_161">161</a></dt> -<dt>Twinning, <a href="#Page_19">19</a></dt> -<dt>Type metal, <a href="#Page_60">60</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_U">U</dt> -<dt>Uintaite, <a href="#Page_229">229</a></dt> -<dt>Uranium, <a href="#Page_89">89</a></dt> -<dt>Uvarovite, <a href="#Page_122">122</a>, <a href="#Page_123">123</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_V">V</dt> -<dt>Vanadium, <a href="#Page_89">89</a></dt> -<dt>Verde antique, <a href="#Page_247">247</a></dt> -<dt>Volcanic ash, <a href="#Page_190">190</a></dt> -<dt>Volcanic blocks, <a href="#Page_191">191</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_W">W</dt> -<dt>Water, <a href="#Page_167">167</a></dt> -<dt>White metal, <a href="#Page_64">64</a></dt> -<dt>Willemite, <a href="#Page_67">67</a></dt> -<dt>Witherite, <a href="#Page_153">153</a></dt> -<dt>Wolframite, <a href="#Page_88">88</a></dt> -<dt>Wood, agatized, <a href="#Page_108">108</a></dt> -<dt>Wood, opalized, <a href="#Page_109">109</a></dt> -<dt>Wood, silicified, <a href="#Page_108">108</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_X">X</dt> -<dt>Xanthosiderite, <a href="#Page_51">51</a></dt> -</dl> -<dl class="index"> -<dt class="center b" id="index_Z">Z</dt> -<dt>Zeolites, <a href="#Page_141">141</a></dt> -<dt>Zinc, <a href="#Page_63">63</a></dt> -<dt>Zinc blende, <a href="#Page_65">65</a></dt> -<dt>Zinc red ore, <a href="#Page_66">66</a></dt> -<dt>Zinc, ruby, <a href="#Page_65">65</a></dt> -<dt>Zincite, <a href="#Page_66">66</a></dt> -<dt>Zircon, <a href="#Page_127">127</a></dt> -</dl> -<div class="pb" id="Page_279">279</div> -<h3 class="plate" id="Plate_Frontispiece">Plate Frontispiece</h3> -<div class="img" id="fig1"> -<img src="images/p01.jpg" alt="" width="539" height="901" /> -<p class="pcap">Tourmaline crystals, growing amid feldspar crystals in a -cavity in granite, from Paris, Me.</p> -</div> -<div class="pb" id="Page_280">280</div> -<h3 class="plate" id="Plate_5">Plate 5</h3> -<div class="img" id="fig2"> -<img src="images/p02.jpg" alt="" width="600" height="518" /> -<p class="pcap">Gold in quartz, from California</p> -</div> -<div class="pb" id="Page_281">281</div> -<h3 class="plate" id="Plate_6">Plate 6</h3> -<div class="img" id="fig3"> -<img src="images/p02a.jpg" alt="" width="600" height="475" /> -<p class="pcap">Native silver in calcite</p> -</div> -<div class="img" id="fig4"> -<img src="images/p02b.jpg" alt="" width="600" height="467" /> -<p class="pcap">Argentite, the black masses throughout the white quartz</p> -</div> -<div class="pb" id="Page_282">282</div> -<h3 class="plate" id="Plate_7">Plate 7</h3> -<div class="img" id="fig5"> -<img src="images/p03.jpg" alt="" width="600" height="577" /> -<p class="pcap">Pyrargyrite as it appears after moderate exposure -to the light.</p> -</div> -<div class="img" id="fig6"> -<img src="images/p03a.jpg" alt="" width="300" height="425" /> -<p class="pcap">Crystal form of Pyrargyrite</p> -</div> -<div class="img" id="fig7"> -<img src="images/p03b.jpg" alt="" width="500" height="511" /> -<p class="pcap">Prousite as it appears after moderate exposure to the light</p> -</div> -<div class="pb" id="Page_283">283</div> -<h3 class="plate" id="Plate_8">Plate 8</h3> -<div class="img" id="fig8"> -<img src="images/p03d.jpg" alt="" width="600" height="463" /> -<p class="pcap">Native copper from Michigan</p> -</div> -<div class="img" id="fig9"> -<img src="images/p03e.jpg" alt="" width="600" height="468" /> -<p class="pcap">Chalcopyrite in tetrahedrons and an occasional octahedron.</p> -</div> -<div class="pb" id="Page_284">284</div> -<h3 class="plate" id="Plate_9">Plate 9</h3> -<div class="img" id="fig10"> -<img src="images/p04.jpg" alt="" width="600" height="555" /> -<p class="pcap">Chalcocite crystals with the bluish tarnish</p> -</div> -<div class="img" id="fig11"> -<img src="images/p04a.jpg" alt="" width="600" height="506" /> -<p class="pcap">Tetrahedrite crystals</p> -</div> -<div class="pb" id="Page_285">285</div> -<h3 class="plate" id="Plate_11">Plate 11</h3> -<div class="img" id="fig12"> -<img src="images/p04c.jpg" alt="" width="600" height="520" /> -<p class="pcap">Cuprite, the red crystals showing characteristic color, -other showing the green tarnish of malachite</p> -</div> -<div class="img" id="fig13"> -<img src="images/p04d.jpg" alt="" width="600" height="468" /> -<p class="pcap">Malachite (green) and azurite (blue), the two minerals -shown together as they very commonly occur</p> -</div> -<div class="pb" id="Page_286">286</div> -<h3 class="plate" id="Plate_12">Plate 12</h3> -<div class="img" id="fig14"> -<img src="images/p05.jpg" alt="" width="600" height="386" /> -<p class="pcap">Limonite</p> -</div> -<div class="img" id="fig15"> -<img src="images/p05a.jpg" alt="" width="300" height="495" /> -<p class="pcap">The crystal form in which goethite is found, -<i>p</i> is the prism faces, <i>b</i> and <i>c</i> are -faces formed by beveling the edges of the prism, <i>o</i> is -the pyramidal face characteristic of the ends</p> -</div> -<div class="pb" id="Page_287">287</div> -<h3 class="plate" id="Plate_13">Plate 13</h3> -<div class="img" id="fig16"> -<img src="images/p05c.jpg" alt="" width="600" height="404" /> -<p class="pcap">Hematite, Clinton iron ore, oolitic</p> -</div> -<div class="img" id="fig17"> -<img src="images/p05d.jpg" alt="" width="600" height="514" /> -<p class="pcap">Siderite crystals</p> -</div> -<div class="pb" id="Page_288">288</div> -<h3 class="plate" id="Plate_15">Plate 15</h3> -<div class="img" id="fig18"> -<img src="images/p06.jpg" alt="" width="600" height="494" /> -<p class="pcap">Pyrite crystals</p> -</div> -<div class="img" id="fig19"> -<img src="images/p06a.jpg" alt="" width="600" height="586" /> -<p class="pcap">Marcasite in concretionary form with radiate structure</p> -</div> -<div class="pb" id="Page_289">289</div> -<h3 class="plate" id="Plate_17">Plate 17</h3> -<div class="img" id="fig20"> -<img src="images/p06c.jpg" alt="" width="600" height="437" /> -<p class="pcap">Galena in crystals</p> -</div> -<div class="img" id="fig21"> -<img src="images/p06d.jpg" alt="" width="600" height="566" /> -<p class="pcap">Pyromorphite crystals (green)</p> -</div> -<div class="pb" id="Page_290">290</div> -<h3 class="plate" id="Plate_19">Plate 19</h3> -<div class="img" id="fig22"> -<img src="images/p07.jpg" alt="" width="600" height="430" /> -<p class="pcap">Sphalerite, some the normal yellow and some crystals with -the reddish tinge. (White is dolomite)</p> -</div> -<div class="img" id="fig23"> -<img src="images/p07a.jpg" alt="" width="600" height="473" /> -<p class="pcap">Zincite</p> -</div> -<div class="pb" id="Page_291">291</div> -<h3 class="plate" id="Plate_21">Plate 21</h3> -<div class="img" id="fig24"> -<img src="images/p07c.jpg" alt="" width="600" height="476" /> -<p class="pcap">Smithsonite in yellow crystals</p> -</div> -<div class="img" id="fig25"> -<img src="images/p07d.jpg" alt="" width="600" height="478" /> -<p class="pcap">Franklinite in octahedral crystals</p> -</div> -<div class="pb" id="Page_292">292</div> -<h3 class="plate" id="Plate_24">Plate 24</h3> -<div class="img" id="fig26"> -<img src="images/p08.jpg" alt="" width="600" height="497" /> -<p class="pcap">Arsenopyrite, showing crystals massed so as to be incompletely -developed</p> -</div> -<div class="img" id="fig27"> -<img src="images/p08a.jpg" alt="" width="600" height="473" /> -<p class="pcap">Realgar as it usually occurs in powdery incrustations</p> -</div> -<div class="pb" id="Page_293">293</div> -<h3 class="plate" id="Plate_25">Plate 25</h3> -<div class="img" id="fig28"> -<img src="images/p08c.jpg" alt="" width="600" height="218" /> -<p class="pcap">Large crystal of stibnite, the light colored face is the one -parallel to which cleavage occurs</p> -</div> -<div class="img" id="fig29"> -<img src="images/p08d.jpg" alt="" width="600" height="489" /> -<p class="pcap">Niccolite as a vein in slate</p> -</div> -<div class="pb" id="Page_294">294</div> -<h3 class="plate" id="Plate_26">Plate 26</h3> -<div class="img" id="fig30"> -<img src="images/p09.jpg" alt="" width="600" height="539" /> -<p class="pcap">Cobaltite, silver color, with pink tinge</p> -</div> -<div class="img" id="fig31"> -<img src="images/p09a.jpg" alt="" width="600" height="408" /> -<p class="pcap">Smaltite, pink is cobalt bloom</p> -</div> -<div class="pb" id="Page_295">295</div> -<h3 class="plate" id="Plate_27">Plate 27</h3> -<div class="img" id="fig32"> -<img src="images/p09d.jpg" alt="" width="600" height="322" /> -<p class="pcap">Carnotite from southwest Colorado</p> -</div> -<div class="img" id="fig33"> -<img src="images/p09e.jpg" alt="" width="600" height="577" /> -<p class="pcap">Cinnabar</p> -</div> -<div class="pb" id="Page_296">296</div> -<h3 class="plate" id="Plate_31">Plate 31</h3> -<div class="img" id="fig34"> -<img src="images/p10.jpg" alt="" width="600" height="503" /> -<p class="pcap">Amethyst, not however deep enough colored for gems</p> -</div> -<div class="img" id="fig35"> -<img src="images/p10a.jpg" alt="" width="424" height="600" /> -<p class="pcap">Jasper, with botryoidal surface</p> -</div> -<div class="pb" id="Page_297">297</div> -<h3 class="plate" id="Plate_32">Plate 32</h3> -<div class="img" id="fig36"> -<img src="images/p10b.jpg" alt="" width="600" height="755" /> -<p class="pcap">Banded Agate from Brazil</p> -</div> -<div class="pb" id="Page_298">298</div> -<h3 class="plate" id="Plate_33">Plate 33</h3> -<div class="img" id="fig37"> -<img src="images/p11.jpg" alt="" width="600" height="441" /> -<p class="pcap">Common Opal from Arizona</p> -</div> -<div class="img" id="fig38"> -<img src="images/p11a.jpg" alt="" width="600" height="485" /> -<p class="pcap">Siliceous sinter or Geyserite from The Yellowstone Park</p> -</div> -<div class="pb" id="Page_299">299</div> -<h3 class="plate" id="Plate_35">Plate 35</h3> -<div class="img" id="fig39"> -<img src="images/p11b.jpg" alt="" width="600" height="439" /> -<p class="pcap">A group of Microcline crystals from Pike’s Peak, Colo.</p> -</div> -<div class="img" id="fig40"> -<img src="images/p11d.jpg" alt="" width="600" height="395" /> -<p class="pcap">Labradorite, showing multiple twinning (the striation), -and the iridescent play of colors</p> -</div> -<div class="pb" id="Page_300">300</div> -<h3 class="plate" id="Plate_36">Plate 36</h3> -<div class="img" id="fig41"> -<img src="images/p12.jpg" alt="" width="289" height="356" /> -<p class="pcap">Crystal form of a pyroxene; <i>a</i> -and <i>b</i> prism faces, <i>m</i> the beveled -edge between two prism faces</p> -</div> -<div class="img" id="fig42"> -<img src="images/p12a.jpg" alt="" width="312" height="313" /> -<p class="pcap">Cross section of a pyroxene crystal showing the lines of intersection -of the two cleavage planes</p> -</div> -<div class="img" id="fig43"> -<img src="images/p12b.jpg" alt="" width="600" height="209" /> -<p class="pcap">Cross sections of pyroxenes, showing typical forms taken by crystals</p> -</div> -<div class="img" id="fig44"> -<img src="images/p12g.jpg" alt="" width="600" height="507" /> -<p class="pcap">Augite crystals, in crystalline limestone</p> -</div> -<div class="pb" id="Page_301">301</div> -<h3 class="plate" id="Plate_38">Plate 38</h3> -<div class="img" id="fig45"> -<img src="images/p12h.jpg" alt="" width="659" height="318" /> -<p class="pcap">The dodecahedron and the 24-sided figure characteristic of garnets</p> -</div> -<div class="img" id="fig46"> -<img src="images/p12i.jpg" alt="" width="600" height="524" /> -<p class="pcap">The garnet, grossularite</p> -</div> -<div class="img" id="fig47"> -<img src="images/p12j.jpg" alt="" width="600" height="338" /> -<p class="pcap">The garnet alamandite</p> -</div> -<div class="pb" id="Page_302">302</div> -<h3 class="plate" id="Plate_39">Plate 39</h3> -<div class="img" id="fig48"> -<img src="images/p13.jpg" alt="" width="489" height="600" /> -<p class="pcap">Beryl of gem quality</p> -</div> -<div class="img" id="fig49"> -<img src="images/p13a.jpg" alt="" width="600" height="479" /> -<p class="pcap">Zircon in syenite</p> -</div> -<div class="pb" id="Page_303">303</div> -<h3 class="plate" id="Plate_40">Plate 40</h3> -<div class="img" id="fig50"> -<img src="images/p13c.jpg" alt="" width="600" height="306" /> -<p class="pcap">Cyanite crystals in schist</p> -</div> -<div class="img" id="fig51"> -<img src="images/p13d.jpg" alt="" width="600" height="524" /> -<p class="pcap">A crystal of mica, showing basal cleavage</p> -</div> -<div class="pb" id="Page_304">304</div> -<h3 class="plate" id="Plate_41">Plate 41</h3> -<div class="img" id="fig52"> -<img src="images/p14.jpg" alt="" width="300" height="547" /> -<p class="pcap">Crystal form typical of topaz</p> -</div> -<div class="img" id="fig53"> -<img src="images/p14a.jpg" alt="" width="439" height="600" /> -<p class="pcap">A topaz crystal from Brazil</p> -</div> -<div class="img" id="fig54"> -<img src="images/p14b.jpg" alt="" width="157" height="300" /> -<p class="pcap">Crystal form typical of staurolite when simple</p> -</div> -<div class="img" id="fig55"> -<img src="images/p14d.jpg" alt="" width="500" height="501" /> -<p class="pcap">A typical twin of staurolite</p> -</div> -<div class="pb" id="Page_305">305</div> -<h3 class="plate" id="Plate_43">Plate 43</h3> -<div class="img" id="fig56"> -<img src="images/p14e.jpg" alt="" width="600" height="450" /> -<p class="pcap">Serpentine</p> -</div> -<div class="img" id="fig57"> -<img src="images/p14f.jpg" alt="" width="600" height="316" /> -<p class="pcap">Chlorite</p> -</div> -<div class="pb" id="Page_306">306</div> -<h3 class="plate" id="Plate_49">Plate 49</h3> -<div class="img" id="fig58"> -<img src="images/p15.jpg" alt="" width="600" height="413" /> -<p class="pcap">Apatite crystals in crystalline calcite</p> -</div> -<div class="img" id="fig59"> -<img src="images/p15a.jpg" alt="" width="500" height="325" /> -<p class="pcap">The ends of apatite crystals showing common modes of termination</p> -</div> -<div class="pb" id="Page_307">307</div> -<h3 class="plate" id="Plate_50">Plate 50</h3> -<div class="img" id="fig60"> -<img src="images/p15b.jpg" alt="" width="600" height="500" /> -<p class="pcap">A group of fluorite crystals</p> -</div> -<div class="img" id="fig61"> -<img src="images/p15d.jpg" alt="" width="600" height="415" /> -<p class="pcap">A group of halite crystals</p> -</div> -<div class="pb" id="Page_308">308</div> -<h3 class="plate" id="Plate_61">Plate 61</h3> -<div class="img" id="fig62"> -<img src="images/p16.jpg" alt="" width="600" height="340" /> -<p class="pcap">Amber</p> -</div> -<div class="img" id="fig63"> -<img src="images/p16a.jpg" alt="" width="600" height="751" /> -<p class="pcap">Two bottles of petroleum, the left hand one with a paraffin -base, the right hand one with an asphalt base</p> -</div> -<div class="pb" id="Page_309">309</div> -<h3 class="plate" id="Plate_65">Plate 65</h3> -<div class="img" id="fig64"> -<img src="images/p16c.jpg" alt="" width="600" height="451" /> -<p class="pcap">Mica schist, with garnets</p> -</div> -<div class="img" id="fig65"> -<img src="images/p16d.jpg" alt="" width="600" height="473" /> -<p class="pcap">Chlorite schist</p> -</div> -<div class="pb" id="Page_310">310</div> -<h3 class="plate" id="Plate_67">Plate 67</h3> -<div class="img" id="fig66"> -<img src="images/p17.jpg" alt="" width="563" height="800" /> -<p class="pcap">Serpentine, composed of serpentine, hematite, and some calcite</p> -</div> -<div class="pb" id="Page_311">311</div> -<h3 class="plate" id="Plate_1">Plate 1</h3> -<h4 class="plate">Basal forms of the isometric system</h4> -<div class="img" id="fig67"> -<img src="images/p17a.jpg" alt="" width="500" height="415" /> -<p class="pcap">Cube</p> -</div> -<div class="img" id="fig68"> -<img src="images/p17c.jpg" alt="" width="498" height="655" /> -<p class="pcap">Octahedron</p> -</div> -<div class="img" id="fig69"> -<img src="images/p17d.jpg" alt="" width="500" height="500" /> -<p class="pcap">Dodecahedron</p> -</div> -<div class="pb" id="Page_312">312</div> -<h3 class="plate" id="Plate_2">Plate 2</h3> -<h4 class="plate">Basal forms of the tetragonal system</h4> -<div class="img" id="fig70"> -<img src="images/p18.jpg" alt="" width="324" height="382" /> -<p class="pcap">A square prism</p> -</div> -<div class="img" id="fig71"> -<img src="images/p18c.jpg" alt="" width="347" height="350" /> -<p class="pcap">Octahedron</p> -</div> -<h4 class="plate">Basal forms of the orthorhombic system</h4> -<div class="img" id="fig72"> -<img src="images/p18d.jpg" alt="" width="373" height="409" /> -<p class="pcap">A Rectangular prism</p> -</div> -<div class="img" id="fig73"> -<img src="images/p18e.jpg" alt="" width="278" height="376" /> -<p class="pcap">Octahedron</p> -</div> -<div class="pb" id="Page_313">313</div> -<h3 class="plate" id="Plate_3">Plate 3</h3> -<h4 class="plate">Basal forms of the monoclinic system</h4> -<div class="img" id="fig74"> -<img src="images/p18f.jpg" alt="" width="262" height="532" /> -<p class="pcap">The rectangular prism askew</p> -</div> -<div class="img" id="fig75"> -<img src="images/p18g.jpg" alt="" width="141" height="340" /> -<p class="pcap">The octahedron</p> -</div> -<div class="img" id="fig76"> -<img src="images/p18h.jpg" alt="" width="345" height="207" /> -<p class="pcap">A cross section of the prism with its edges beveled so that -the <i>b</i> faces are obliterated by the <i>m</i> faces, and a six-sided prism -is formed (pseudo-hexagonal)</p> -</div> -<div class="img" id="fig77"> -<img src="images/p18i.jpg" alt="" width="376" height="551" /> -<p class="pcap">Basal form of the triclinic system</p> -</div> -<div class="pb" id="Page_314">314</div> -<h3 class="plate" id="Plate_4">Plate 4</h3> -<h4 class="plate">Basal forms of the hexagonal system</h4> -<div class="img" id="fig78"> -<img src="images/p19.jpg" alt="" width="260" height="582" /> -<p class="pcap">The six-sided prism</p> -</div> -<div class="img" id="fig79"> -<img src="images/p19a.jpg" alt="" width="297" height="527" /> -<p class="pcap">The double pyramid</p> -</div> -<div class="img" id="fig80"> -<img src="images/p19d.jpg" alt="" width="334" height="340" /> -<p class="pcap">The rhombohedron</p> -</div> -<div class="pb" id="Page_315">315</div> -<h3 class="plate" id="Plate_10">Plate 10</h3> -<div class="img" id="fig81"> -<img src="images/p19f.jpg" alt="" width="532" height="222" /> -<p class="pcap">Tetrahedrons showing characteristic manner in which -tetrahedrite occurs</p> -</div> -<div class="img" id="fig82"> -<img src="images/p19g.jpg" alt="" width="464" height="413" /> -<p class="pcap">A cube with the edges beveled and -the corners cut in a form characteristic of cuprite</p> -</div> -<div class="pb" id="Page_316">316</div> -<h3 class="plate" id="Plate_30">Plate 30</h3> -<div class="img" id="fig83"> -<img src="images/p20.jpg" alt="" width="600" height="601" /> -<p class="pcap">Two intergrowing or twinned quartz crystals</p> -</div> -<div class="img" id="fig84"> -<img src="images/p20b.jpg" alt="" width="300" height="547" /> -<p class="pcap">Diagram of the typical quartz crystal, <i>p</i> prism faces, -<i>l</i> left hand rhombohedron, <i>r</i> right hand rhombohedron</p> -</div> -<div class="img" id="fig85"> -<img src="images/p20c.jpg" alt="" width="300" height="516" /> -<p class="pcap">A quartz crystal on which the left hand rhombohedron -is represented by small faces while the right hand rhombohedron has large faces</p> -</div> -<div class="pb" id="Page_317">317</div> -<h3 class="plate" id="Plate_14">Plate 14</h3> -<div class="img" id="fig86"> -<img src="images/p20d.jpg" alt="" width="500" height="284" /> -<p class="pcap">Crystal forms of hematite, <i>A</i> the rhombohedron with -the edges beveled; <i>B</i> the tabular form, resulting from the -excessive development of the two <i>o</i> faces opposite each -other</p> -</div> -<div class="img" id="fig87"> -<img src="images/p20e.jpg" alt="" width="400" height="382" /> -<p class="pcap">A typical crystal of magnetite</p> -</div> -<div class="img" id="fig88"> -<img src="images/p20f.jpg" alt="" width="300" height="325" /> -<p class="pcap">The rhombohedron typical of siderite</p> -</div> -<div class="pb" id="Page_318">318</div> -<h3 class="plate" id="Plate_16">Plate 16</h3> -<div class="img" id="fig89"> -<img src="images/p21.jpg" alt="" width="542" height="498" /> -<p class="pcap">The pyritohedron</p> -</div> -<div class="img" id="fig90"> -<img src="images/p21d.jpg" alt="" width="534" height="465" /> -<p class="pcap">The pyritohedron with certain of its edges beveled by the cube faces, to -show the relationship of these two forms</p> -</div> -<div class="pb" id="Page_319">319</div> -<h3 class="plate" id="Plate_18">Plate 18</h3> -<h4 class="plate">Typical forms for cerrusite</h4> -<div class="img" id="fig91"> -<img src="images/p21e.jpg" alt="" width="293" height="417" /> -<p class="pcap">The pyramid, <i>n</i> the -prism face, <i>m</i> the beveled prism, <i>p</i> the octahedral -face, and <i>o</i> the edge of the octahedral faces beveled</p> -</div> -<div class="img" id="fig92"> -<img src="images/p21f.jpg" alt="" width="219" height="332" /> -<p class="pcap">The simple type of twinning</p> -</div> -<div class="img" id="fig93"> -<img src="images/p21g.jpg" alt="" width="374" height="424" /> -<p class="pcap">A multiple twin where three crystals grow through each other</p> -</div> -<div class="img" id="fig94"> -<img src="images/p21i.jpg" alt="" width="500" height="531" /> -<p class="pcap">Forms in which anglesite occurs: <i>l</i> the pyramid face, <i>p</i> -the prism face, <i>o</i> the vertical edge of the prism beveled, -<i>m</i> the horizontal edge of the prism beveled, <i>n</i> a further -beveling of the horizontal edge of the prism. <i>D</i> the -tabular, <i>E</i> the prismatic form</p> -</div> -<div class="pb" id="Page_320">320</div> -<h3 class="plate" id="Plate_20">Plate 20</h3> -<div class="img" id="fig95"> -<img src="images/p22.jpg" alt="" width="515" height="519" /> -<p class="pcap">A characteristic form in which sphalerite -may occur; being the combination of, <i>d</i> the -dodecahedron, <i>o</i> the octahedron, and <i>t</i>, a 24-sided figure</p> -</div> -<div class="img" id="fig96"> -<img src="images/p22b.jpg" alt="" width="351" height="393" /> -<p class="pcap">Characteristic form for zincite -crystals, <i>n</i> the hexagonal -prism, and <i>p</i> pyramidal faces on it</p> -</div> -<div class="img" id="fig97"> -<img src="images/p22d.jpg" alt="" width="221" height="437" /> -<p class="pcap">Typical form of crystal of willemite: -<i>p</i> the prism, <i>r</i> rhombohedron faces on -end, ½ <i>r</i> a second lower rhombohedron</p> -</div> -<div class="pb" id="Page_321">321</div> -<h3 class="plate" id="Plate_22">Plate 22</h3> -<div class="img" id="fig98"> -<img src="images/p22f.jpg" alt="" width="600" height="569" /> -<p class="pcap">Moss agates, showing the dendritic growth -of manganitic minerals, like manganite or pyrolusite</p> -</div> -<div class="img"> -<img src="images/p22g.jpg" alt="Moss agates" width="600" height="321" /> -</div> -<div class="img" id="fig99"> -<img src="images/p22n.jpg" alt="" width="247" height="400" /> -<p class="pcap">Crystal form of manganite</p> -</div> -<div class="pb" id="Page_322">322</div> -<h3 class="plate" id="Plate_23">Plate 23</h3> -<div class="img" id="fig100"> -<img src="images/p23.jpg" alt="" width="600" height="439" /> -<p class="pcap">Crystals of green corundum in syenite, from Montana</p> -</div> -<div class="img" id="fig101"> -<img src="images/p23a.jpg" alt="" width="479" height="601" /> -<p class="pcap">Typical crystal forms of corundum: <i>A</i> the elongated -prism with the alternate corners cut by -rhombohedral faces, <i>B</i> the tabular prism, <i>C</i> the -double pyramid</p> -</div> -<div class="pb" id="Page_323">323</div> -<h3 class="plate" id="Plate_28">Plate 28</h3> -<div class="img" id="fig102"> -<img src="images/p23e.jpg" alt="" width="600" height="694" /> -<p class="pcap">Cassiterite, twinned crystals</p> -</div> -<div class="img" id="fig103"> -<img src="images/p23f.jpg" alt="" width="274" height="395" /> -<p class="pcap">The crystal form in which both -cassiterite and rutile occur when in -simple crystals, <i>p</i> prism faces, <i>m</i> -beveling of the prism, <i>o</i> octahedral -face, <i>n</i> beveling of the edge between -octahedral faces</p> -</div> -<div class="img" id="fig104"> -<img src="images/p23g.jpg" alt="" width="255" height="380" /> -<p class="pcap">Multiple twinning characteristic of rutile</p> -</div> -<div class="pb" id="Page_324">324</div> -<h3 class="plate" id="Plate_29">Plate 29</h3> -<div class="img" id="fig105"> -<img src="images/p24a1.jpg" alt="" width="600" height="474" /> -<p class="pcap">Crystal of Spinel</p> -</div> -<h4 class="plate">Crystal forms in which dolomite occurs</h4> -<div class="img" id="fig106"> -<img src="images/p24a2.jpg" alt="" width="365" height="296" /> -<p class="pcap"><i>A</i> the cleavage form, rhombohedron with the faces curved</p> -</div> -<div class="img" id="fig107"> -<img src="images/p24a4.jpg" alt="" width="338" height="256" /> -<p class="pcap"><i>B</i> the rhombohedron with the corners cut, as it often occurs</p> -</div> -<div class="img" id="fig108"> -<img src="images/p24a5.jpg" alt="" width="158" height="268" /> -<p class="pcap"><i>C</i> the form found in gypsum or anhydrite</p> -</div> -<div class="pb" id="Page_325">325</div> -<h3 class="plate" id="Plate_34">Plate 34</h3> -<div class="img" id="fig109"> -<img src="images/p24b1.jpg" alt="" width="600" height="485" /> -<p class="pcap">Orthoclase, a cleavage piece, <i>a</i> and <i>b</i> the perfect -cleavage planes, and <i>c</i> the imperfect cleavage plane</p> -</div> -<h4 class="plate">Crystal forms of orthoclase</h4> -<div class="img" id="fig110"> -<img src="images/p24b2.jpg" alt="" width="169" height="283" /> -<p class="pcap"><i>A</i> the simple crystal</p> -</div> -<div class="img" id="fig111"> -<img src="images/p24b4.jpg" alt="" width="170" height="284" /> -<p class="pcap"><i>B</i> the twinned form</p> -</div> -<div class="img" id="fig112"> -<img src="images/p24b5.jpg" alt="" width="167" height="282" /> -<p class="pcap"><i>C</i> the twinned form in which the crystals are intergrowing</p> -</div> -<div class="img" id="fig113"> -<img src="images/p24b6.jpg" alt="" width="356" height="428" /> -<p class="pcap">Diagram of a multiple twin of a plagioclase feldspar</p> -</div> -<div class="pb" id="Page_326">326</div> -<h3 class="plate" id="Plate_37">Plate 37</h3> -<h4 class="plate">Diagrams of amphibole crystals</h4> -<div class="img" id="fig114"> -<img src="images/p25.jpg" alt="" width="194" height="501" /> -<p class="pcap"><i>A</i> a typical crystal</p> -</div> -<div class="img" id="fig115"> -<img src="images/p25a.jpg" alt="" width="295" height="454" /> -<p class="pcap"><i>B</i> cross section showing the intersection of cleavage planes</p> -</div> -<div class="img" id="fig116"> -<img src="images/p25a2.jpg" alt="" width="360" height="297" /> -<p class="pcap"><i>C</i> and <i>D</i> cross sections to show variations in outline</p> -</div> -<div class="img" id="fig117"> -<img src="images/p25b1.jpg" alt="" width="600" height="335" /> -<p class="pcap">Tremolite in silky -fibrous crystals. Asbestos</p> -</div> -<div class="img" id="fig118"> -<img src="images/p25b2.jpg" alt="" width="600" height="530" /> -<p class="pcap">Hornblende crystals in quartzite</p> -</div> -<div class="pb" id="Page_327">327</div> -<h3 class="plate" id="Plate_42">Plate 42</h3> -<div class="img" id="fig119"> -<img src="images/p25b3.jpg" alt="" width="600" height="368" /> -<p class="pcap">Epidote crystals</p> -</div> -<div class="img" id="fig120"> -<img src="images/p25c3.jpg" alt="" width="406" height="372" /> -<p class="pcap">Typical forms of epidote crystals; -<i>p</i> prism faces, <i>m</i>, <i>n</i>, <i>x</i>, and -<i>y</i> beveled edges of the prism, -<i>o</i> octahedral faces</p> -</div> -<h4 class="plate">Typical forms of tourmaline</h4> -<div class="img" id="fig121"> -<img src="images/p25c4.jpg" alt="" width="600" height="642" /> -<p class="pcap"><i>A</i> side view; <i>B</i> -and <i>C</i> ends to show terminations; -<i>p</i> prism faces, -<i>m</i> beveling of prism -edges, <i>r</i> a low rhombohedron -on the end, <i>s</i> the opposite rhombohedron, <i>b</i> basal -face, and the other faces represent bevelings</p> -</div> -<div class="pb" id="Page_328">328</div> -<h3 class="plate" id="Plate_48">Plate 48</h3> -<div class="img" id="fig122"> -<img src="images/p26.jpg" alt="" width="600" height="474" /> -<p class="pcap">A group of barite crystals</p> -</div> -<div class="img" id="fig123"> -<img src="images/p26a.jpg" alt="" width="461" height="169" /> -<p class="pcap">Outline of the typical tabular barite crystal</p> -</div> -<div class="img" id="fig124"> -<img src="images/p26b.jpg" alt="" width="230" height="336" /> -<p class="pcap">The six-sided double pyramid, -composed of three interpenetrating -crystals, typical of witherite and strontianite</p> -</div> -<div class="pb" id="Page_329">329</div> -<h3 class="plate" id="Plate_44">Plate 44</h3> -<div class="img" id="fig125"> -<img src="images/p26c.jpg" alt="" width="330" height="343" /> -<p class="pcap">The typical form of analcite</p> -</div> -<div class="img" id="fig126"> -<img src="images/p26d.jpg" alt="" width="194" height="376" /> -<p class="pcap">A typical natrolite crystal</p> -</div> -<div class="img" id="fig127"> -<img src="images/p26e.jpg" alt="" width="175" height="432" /> -<p class="pcap">The typical crystal form of stilbite</p> -</div> -<div class="img" id="fig128"> -<img src="images/p26f.jpg" alt="" width="213" height="438" /> -<p class="pcap">A sheaf-like bundle of fibrous crystals, typical of stilbite</p> -</div> -<div class="pb" id="Page_330">330</div> -<h3 class="plate" id="Plate_45">Plate 45</h3> -<div class="img" id="fig129"> -<img src="images/p27.jpg" alt="" width="600" height="388" /> -<p class="pcap">A group of calcite crystals</p> -</div> -<h4 class="plate">Typical forms of calcite</h4> -<div class="img" id="fig130"> -<img src="images/p27a.jpg" alt="" width="321" height="259" /> -<p class="pcap"><i>A</i> the rhombohedron formed by cleavage</p> -</div> -<div class="img" id="fig131"> -<img src="images/p27b.jpg" alt="" width="304" height="223" /> -<p class="pcap"><i>B</i> a rhombohedral crystal truncated by the basal plane</p> -</div> -<div class="img" id="fig132"> -<img src="images/p27c.jpg" alt="" width="194" height="384" /> -<p class="pcap"><i>C</i> the scalenohedron</p> -</div> -<div class="img" id="fig133"> -<img src="images/p27d.jpg" alt="" width="185" height="273" /> -<p class="pcap"><i>D</i> the scalenohedron truncated by the rhombohedron</p> -</div> -<div class="img" id="fig134"> -<img src="images/p27g.jpg" alt="" width="197" height="398" /> -<p class="pcap"><i>E</i> the scalenohedron on a prism</p> -</div> -<div class="pb" id="Page_331">331</div> -<h3 class="plate" id="Plate_46">Plate 46</h3> -<h4 class="plate">Typical forms of aragonite</h4> -<div class="img" id="fig135"> -<img src="images/p27i.jpg" alt="" width="194" height="371" /> -<p class="pcap"><i>A</i> the simple crystal</p> -</div> -<div class="img" id="fig136"> -<img src="images/p27l.jpg" alt="" width="75" height="386" /> -<p class="pcap"><i>B</i> a needle-like form, twinned</p> -</div> -<div class="img" id="fig137"> -<img src="images/p27m.jpg" alt="" width="178" height="197" /> -<p class="pcap"><i>C</i> cross section to show how the form may appear six-sided</p> -</div> -<div class="img" id="fig138"> -<img src="images/p27n.jpg" alt="" width="290" height="129" /> -<p class="pcap">Typical form of the anhydrite crystal</p> -</div> -<div class="pb" id="Page_332">332</div> -<h3 class="plate" id="Plate_47">Plate 47</h3> -<div class="img" id="fig139"> -<img src="images/p28.jpg" alt="" width="600" height="436" /> -<p class="pcap">A piece of gypsum looking on the surface of the perfect -cleavage, and showing the two other cleavages as lines, -intersecting at 66°. Twinning is also shown</p> -</div> -<div class="img" id="fig140"> -<img src="images/p28c.jpg" alt="" width="250" height="576" /> -<p class="pcap">A simple crystal of gypsum</p> -</div> -<div class="img" id="fig141"> -<img src="images/p28d.jpg" alt="" width="300" height="579" /> -<p class="pcap">Twin crystals of gypsum</p> -</div> -<div class="pb" id="Page_333">333</div> -<h3 class="plate" id="Plate_51">Plate 51</h3> -<div class="img" id="fig142"> -<img src="images/p28e.jpg" alt="" width="600" height="570" /> -<p class="pcap">Sulphur crystals</p> -</div> -<div class="img" id="fig143"> -<img src="images/p28f.jpg" alt="" width="500" height="484" /> -<p class="pcap">Ice crystals, the top one, the end of a hexagonal prism; -the two lower figures multiple twins as in snow flakes</p> -</div> -<div class="pb" id="Page_334">334</div> -<h3 class="plate" id="Plate_52">Plate 52</h3> -<div class="img" id="fig144"> -<img src="images/p29.jpg" alt="" width="465" height="901" /> -<p class="pcap">The Devil’s Tower, Wyoming, an example of igneous -rock with columnar structure, and resting on sedimentary -rocks. Courtesy of the U. S. Geological Survey</p> -</div> -<div class="pb" id="Page_335">335</div> -<h3 class="plate" id="Plate_53">Plate 53</h3> -<div class="img" id="fig145"> -<img src="images/p29b.jpg" alt="" width="600" height="406" /> -<p class="pcap">A coarse granite</p> -</div> -<div class="img" id="fig146"> -<img src="images/p29c.jpg" alt="" width="600" height="365" /> -<p class="pcap">Graphic granite</p> -</div> -<div class="pb" id="Page_336">336</div> -<h3 class="plate" id="Plate_54">Plate 54</h3> -<div class="img" id="fig147"> -<img src="images/p30.jpg" alt="" width="600" height="554" /> -<p class="pcap">Syenite</p> -</div> -<div class="img" id="fig148"> -<img src="images/p30a.jpg" alt="" width="600" height="457" /> -<p class="pcap">Gabbro</p> -</div> -<div class="pb" id="Page_337">337</div> -<h3 class="plate" id="Plate_55">Plate 55</h3> -<div class="img" id="fig149"> -<img src="images/p30c.jpg" alt="" width="600" height="429" /> -<p class="pcap">Basalt-porphyry. The large white crystals are phenocrysts -of plagioclase feldspar</p> -</div> -<div class="img" id="fig150"> -<img src="images/p30d.jpg" alt="" width="600" height="529" /> -<p class="pcap">Basalt-obsidian</p> -</div> -<div class="pb" id="Page_338">338</div> -<h3 class="plate" id="Plate_56">Plate 56</h3> -<div class="img" id="fig151"> -<img src="images/p31.jpg" alt="" width="600" height="482" /> -<p class="pcap">Amgydoloid</p> -</div> -<div class="pb" id="Page_339">339</div> -<h3 class="plate" id="Plate_57">Plate 57</h3> -<div class="img" id="fig152"> -<img src="images/p31a.jpg" alt="" width="500" height="887" /> -<p class="pcap">The north face of Scott’s Bluff, Neb., showing sedimentary -sandstones above and clays below. The type of -erosion is characteristic of arid regions. Courtesy of -the U. S. Geological Survey</p> -</div> -<div class="pb" id="Page_340">340</div> -<h3 class="plate" id="Plate_58">Plate 58</h3> -<div class="img" id="fig153"> -<img src="images/p32.jpg" alt="" width="600" height="503" /> -<p class="pcap">Breccia</p> -</div> -<div class="img" id="fig154"> -<img src="images/p32a.jpg" alt="" width="600" height="470" /> -<p class="pcap">Conglomerate</p> -</div> -<div class="pb" id="Page_341">341</div> -<h3 class="plate" id="Plate_59">Plate 59</h3> -<div class="img" id="fig155"> -<img src="images/p32c.jpg" alt="" width="600" height="531" /> -<p class="pcap">Calcareous shale</p> -</div> -<div class="img" id="fig156"> -<img src="images/p32d.jpg" alt="" width="600" height="374" /> -<p class="pcap">Coquina</p> -</div> -<div class="pb" id="Page_342">342</div> -<h3 class="plate" id="Plate_60">Plate 60</h3> -<div class="img" id="fig157"> -<img src="images/p33.jpg" alt="" width="600" height="497" /> -<p class="pcap">Foramenifera from Chalk; enlarged about 25 diameters</p> -</div> -<div class="img" id="fig158"> -<img src="images/p34.jpg" alt="" width="600" height="483" /> -<p class="pcap">Encrinal Limestone; fragments of the stems, arms and -body of Crinoids</p> -</div> -<div class="pb" id="Page_343">343</div> -<h3 class="plate" id="Plate_62">Plate 62</h3> -<div class="img" id="fig159"> -<img src="images/p35.jpg" alt="" width="483" height="502" /> -<p class="pcap"><i>A</i> diatomaceous earth magnified 50 times</p> -</div> -<div class="img" id="fig160"> -<img src="images/p36.jpg" alt="" width="279" height="600" /> -<p class="pcap"><i>B</i> and <i>C</i> two diatoms from -the above enlarged 250 times. After -Gravelle, by the courtesy of Natural History</p> -</div> -<div class="pb" id="Page_344">344</div> -<h3 class="plate" id="Plate_63">Plate 63</h3> -<div class="img" id="fig161"> -<img src="images/p38.jpg" alt="" width="900" height="480" /> -<p class="pcap">A metamorphic rock, showing the contortion of layers due to expansion under heat</p> -</div> -<div class="pb" id="Page_345">345</div> -<h3 class="plate" id="Plate_64">Plate 64</h3> -<div class="img" id="fig162"> -<img src="images/p38a.jpg" alt="" width="600" height="349" /> -<p class="pcap">A conglomerate partly metamorphosed to a gneiss. Note -the flattened pebbles and the alternation of the intermediate -material to mica scales, etc.</p> -</div> -<div class="img" id="fig163"> -<img src="images/p38d.jpg" alt="" width="600" height="659" /> -<p class="pcap">A typical gneiss</p> -</div> -<div class="pb" id="Page_346">346</div> -<h3 class="plate" id="Plate_66">Plate 66</h3> -<div class="img" id="fig164"> -<img src="images/p39.jpg" alt="" width="600" height="400" /> -<p class="pcap">Phyllite</p> -</div> -<div class="img" id="fig165"> -<img src="images/p39a.jpg" alt="" width="600" height="643" /> -<p class="pcap">A white marble, with black streaks due to graphite</p> -</div> -<div class="pb" id="Page_347">347</div> -<h3 class="plate" id="Plate_68">Plate 68</h3> -<div class="img" id="fig166"> -<img src="images/p39c.jpg" alt="" width="600" height="512" /> -<p class="pcap">Claystones, simple and compound</p> -</div> -<div class="img" id="fig167"> -<img src="images/p39d.jpg" alt="" width="600" height="564" /> -<p class="pcap">A line concretion, which on splitting disclosed a fern leaf -of the age of the coal measures</p> -</div> -<div class="pb" id="Page_348">348</div> -<h3 class="plate" id="Plate_69">Plate 69</h3> -<div class="img" id="fig168"> -<img src="images/p40.jpg" alt="" width="600" height="542" /> -<p class="pcap">A septeria from Seneca Lake, N. Y.</p> -</div> -<div class="img" id="fig169"> -<img src="images/p40a.jpg" alt="" width="600" height="666" /> -<p class="pcap">Pisolite</p> -</div> -<div class="pb" id="Page_349">349</div> -<h3 class="plate" id="Plate_70">Plate 70</h3> -<div class="img" id="fig170"> -<img src="images/p40c.jpg" alt="" width="600" height="622" /> -<p class="pcap">A geode filled with quartz crystals</p> -</div> -<div class="pb" id="Page_350">350</div> -<h3 class="plate" id="Plate_71">Plate 71</h3> -<div class="img" id="fig171"> -<img src="images/p41.jpg" alt="" width="600" height="472" /> -<p class="pcap">A quartz pebble from the bed of a New England brook</p> -</div> -<div class="img" id="fig172"> -<img src="images/p41a.jpg" alt="" width="600" height="527" /> -<p class="pcap">A pebble of schist and granite from the foot of Mt. Toby, -Mass.</p> -</div> -<div class="pb" id="Page_351">351</div> -<h3 class="plate" id="Plate_72">Plate 72</h3> -<div class="img" id="fig173"> -<img src="images/p41c.jpg" alt="" width="600" height="436" /> -<p class="pcap">An iron-nickel meteorite, of 23 lbs. which fell in Claiborne -Co., Tenn.</p> -</div> -<div class="img" id="fig174"> -<img src="images/p41d.jpg" alt="" width="600" height="524" /> -<p class="pcap">An etched slice of an iron meteorite which fell in Reed -City, Osceola Co., Mich.</p> -</div> -<div class="pb" id="Page_352">352</div> -<h3 class="plate" id="Plate_73">Plate 73</h3> -<div class="img" id="fig175"> -<img src="images/p42.jpg" alt="" width="800" height="562" /> -<p class="pcap">A stony meteorite, about natural size, which fell in 1875, in Iowa Co., Iowa</p> -</div> -<hr /> -<h3 class="center">PUTNAM’S -<br />NATURE FIELD BOOKS -<br />Companion books to this one</h3> -<table class="center" summary=""> -<tr><td class="l">Mathews </td><td class="l">American Wild Flowers</td></tr> -<tr><td class="l"> </td><td class="l">American Trees and Shrubs</td></tr> -<tr><td class="l"> </td><td class="l">Wild Birds and Their Music</td></tr> -<tr><td class="l">Durand </td><td class="l">Wild Flowers in Homes and Gardens</td></tr> -<tr><td class="l"> </td><td class="l">My Wild Flower Garden</td></tr> -<tr><td class="l"> </td><td class="l">Common Ferns</td></tr> -<tr><td class="l">Lutz </td><td class="l">Insects</td></tr> -<tr><td class="l">Loomis </td><td class="l">Rocks and Minerals</td></tr> -<tr><td class="l">Eliot </td><td class="l">Birds of the Pacific Coast</td></tr> -<tr><td class="l">Armstrong </td><td class="l">Western Wild Flowers</td></tr> -<tr><td class="l">Alexander </td><td class="l">Birds of the Ocean</td></tr> -<tr><td class="l">Anthony </td><td class="l">North American Mammals</td></tr> -<tr><td class="l">Thomas </td><td class="l">Common Mushrooms</td></tr> -<tr><td class="l">Sturgis </td><td class="l">Birds of the Panama Canal Zone</td></tr> -<tr><td class="l">Miner </td><td class="l">Seashore Life</td></tr> -<tr><td class="l">Breder </td><td class="l">Marine Fishes of the Atlantic Coast</td></tr> -<tr><td class="l">Morgan </td><td class="l">Ponds and Streams</td></tr> -<tr><td class="l">Longyear </td><td class="l">Rocky Mountain Trees and Shrubs</td></tr> -<tr><td class="l">Olcott<br />Putnam </td><td class="l">Field Book of the Skies</td></tr> -<tr><td class="l">Beebe<br />Tee-Van </td><td class="l">The Shore Fishes of Bermuda</td></tr> -<tr><td class="l">Schrenkeisen </td><td class="l">Fresh-Water Fishes of North America North of Mexico</td></tr> -</table> -<h2>Transcriber’s Notes</h2> -<ul> -<li>Retained publication information from the printed edition: this eBook is public-domain in the country of publication.</li> -<li>In the text versions only, text in italics is delimited by _underscores_.</li> -<li>Silently corrected a few typos.</li> -<li>Reconstructed an image caption (Pisolite) on Plate 69.</li> -<li>Generated a cover image based on elements in the book.</li> -</ul> - - - - - - - -<pre> - - - - - -End of the Project Gutenberg EBook of Field Book of Common Rocks and Minerals, by -Frederic Brewster Loomis and Walter Everett Corbin - -*** END OF THIS PROJECT GUTENBERG EBOOK FIELD BOOK OF COMMON ROCKS *** - -***** This file should be named 55382-h.htm or 55382-h.zip ***** -This and all associated files of various formats will be found in: - http://www.gutenberg.org/5/5/3/8/55382/ - -Produced by Stephen Hutcheson, Dave Morgan and the Online -Distributed Proofreading Team at http://www.pgdp.net - -Updated editions will replace the previous one--the old editions will -be renamed. - -Creating the works from print editions not protected by U.S. copyright -law means that no one owns a United States copyright in these works, -so the Foundation (and you!) can copy and distribute it in the United -States without permission and without paying copyright -royalties. 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