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-*** START OF THE PROJECT GUTENBERG EBOOK 60990 ***
-
-[Illustration:
-
-_PLATE I_
-_Frontispiece_
-
-GEM-STONES]
-
-
-
-
- GEM-STONES
-
- AND THEIR DISTINCTIVE CHARACTERS
-
-
- BY
-
- G. F. HERBERT SMITH
- M.A., D.Sc.
- OF THE BRITISH MUSEUM (NATURAL HISTORY)
-
-
- WITH MANY DIAGRAMS AND THIRTY-TWO PLATES
- OF WHICH THREE ARE IN COLOUR
-
-
- THIRD EDITION
-
-
- METHUEN & CO. LTD.
- 36 ESSEX STREET W.C.
- LONDON
-
-
- _First Published_ _March 21st 1910_
- _Second Edition_ _June_ _1913_
- _Third Edition_ _1919_
-
-
-
-
- PREFACE
-
-
-In this edition the opportunity has been taken to correct a few
-misprints and mistakes that have been discovered in the first, and to
-alter slightly one or two paragraphs, but otherwise no change has been
-made. G. F. H. S. WANDSWORTH COMMON, S.W.
-
-
-
-
- PREFACE TO THE FIRST EDITION
-
-
-It has been my endeavour to provide in this book a concise, yet
-sufficiently complete, account of the physical characters of the
-mineral species which find service in jewellery, and of the methods
-available for determining their principal physical constants to enable
-a reader, even if previously unacquainted with the subject, to have
-at hand all the information requisite for the sure identification of
-any cut stone which may be met with. For several reasons I have dealt
-somewhat more fully with the branches of science closely connected with
-the properties of crystallized matter than has been customary hitherto
-in even the most comprehensive books on precious stones. Recent years
-have witnessed many changes in the jewellery world. Gem-stones are no
-longer entirely drawn from a few well-marked mineral species, which
-are, on the whole, easily distinguishable from one another, and it
-becomes increasingly difficult for even the most experienced eye to
-recognize a cut stone with unerring certainty. So long as the only
-confusion lay between precious stones and paste imitations an ordinary
-file was the solitary piece of apparatus required by the jeweller, but
-now recourse must be had to more discriminative tests, such as the
-refractive index or the specific gravity, the determination of which
-calls for a little knowledge and skill. Concurrently, a keener interest
-is being taken in the scientific aspect of gem-stones by the public at
-large, who are attracted to them mainly by æsthetic considerations.
-
-While the treatment has been kept as simple as possible, technical
-expressions, where necessary, have not been avoided, but their meanings
-have been explained, and it is hoped that their use will not prove
-stumbling-blocks to the novice. Unfamiliar words of this kind often
-give a forbidding air to a new subject, but they are used merely to
-avoid circumlocution, and not, like the incantations of a wizard, to
-veil the difficulties in still deeper gloom. For actual practical work
-the pages on the refractometer and its use and the method of heavy
-liquids for the determination of specific gravities, and the tables of
-physical constants at the end of the book, with occasional reference,
-in case of doubt, to the descriptions of the several species alone
-are required; other methods—such as the prismatic mode of measuring
-refractive indices, or the hydrostatic way of finding specific
-gravities—which find a place in the ordinary curriculum of a physics
-course are described in their special application to gem-stones, but
-they are not so suitable for workshop practice. Since the scope of the
-book is confined mainly to the stones as they appear on the market,
-little has been said about their geological occurrence; the case of
-diamond, however, is of exceptional interest and has been more fully
-treated. The weights stated for the historical diamonds are those
-usually published, and are probably in many instances far from correct,
-but they serve to give an idea of the sizes of the stones; the English
-carat is the unit used, and the numbers must be increased by about 2½
-per cent. if the weights be expressed in metric carats. The prices
-quoted for the various species must only be regarded as approximate,
-since they may change from year to year, or even day to day, according
-to the state of trade and the whim of fashion.
-
-The diagram on Plate II and most of the crystal drawings were made
-by me. The remaining drawings are the work of Mr. H. H. Penton. He
-likewise prepared the coloured drawings of cut stones which appear
-on the three coloured plates, his models, with two exceptions, being
-selected from the cut specimens in the Mineral Collection of the
-British Museum by permission of the Trustees. Unfortunately, the
-difficulties that still beset the reproduction of pictures in colour
-have prevented full justice being done to the faithfulness of his
-brush. I highly appreciate the interest he took in the work, and the
-care and skill with which it was executed. My thanks are due to the
-De Beers Consolidated Mines Co. Ltd., and to Sir Henry A. Miers,
-F.R.S., Principal of the University of London, for the illustrations
-of the Kimberley and Wesselton diamond mines, and of the methods and
-apparatus employed in breaking up and concentrating the blue ground;
-to Messrs. I. J. Asscher & Co. for the use of the photograph of the
-Cullinan diamond; to Mr. J. H. Steward for the loan of the block of the
-refractometer; and to Mr. H. W. Atkinson for the illustration of the
-diamond-sorting machine. My colleague, Mr. W. Campbell Smith, B.A., has
-most kindly read the proof-sheets, and has been of great assistance in
-many ways. I hope that, thanks to his invaluable help, the errors in
-the book which may have escaped notice will prove few in number and
-unimportant in character. To Mr. Edward Hopkins I owe an especial debt
-of gratitude for his cheerful readiness to assist me in any way in
-his power. He read both the manuscript and the proof-sheets, and the
-information with regard to the commercial and practical side of the
-subject was very largely supplied by him. He also placed at my service
-a large number of photographs, some of which—for instance, those
-illustrating the cutting of stones—he had specially taken for me, and
-he procured for me the jewellery designs shown on Plates IV and V.
-
-If this book be found by those engaged in the jewellery trade helpful
-in their everyday work, and if it wakens in readers generally an
-appreciation of the variety of beautiful minerals suitable for gems,
-and an interest in the wondrous qualities of crystallized substances, I
-shall be more than satisfied.
- G. F. H. S.
- WANDSWORTH COMMON, S.W.
-
-
-
-
- CONTENTS
-
-
- CHAP. PAGE
- I. INTRODUCTION 1
-
-
- PART I—SECTION A
-
- THE CHARACTERS OF GEM-STONES
-
- II. CRYSTALLINE FORM 6
-
- III. REFLECTION, REFRACTION, AND DISPERSION 14
-
- IV. MEASUREMENT OF REFRACTIVE INDICES 21
-
- V. LUSTRE AND SHEEN 37
-
- VI. DOUBLE REFRACTION 40
-
- VII. ABSORPTION EFFECTS: COLOUR, DICHROISM,ETC. 53
-
- VIII. SPECIFIC GRAVITY 63
-
- IX. HARDNESS AND CLEAVABILITY 78
-
- X. ELECTRICAL CHARACTERS 82
-
-
- PART I—SECTION B
-
- THE TECHNOLOGY OF GEM-STONES
-
- XI. UNIT OF WEIGHT 84
-
- XII. FASHIONING OF GEM-STONES 88
-
- XIII. NOMENCLATURE OF PRECIOUS STONES 109
-
- XIV. MANUFACTURED STONES 113
-
- XV. IMITATION STONES 124
-
-
- PART II—SECTION A
-
- PRECIOUS STONES
-
- XVI. DIAMOND 128
-
- XVII. OCCURRENCE OF DIAMOND 137
-
- XVIII. HISTORICAL DIAMONDS 157
-
- XIX. CORUNDUM (_Sapphire_, _Ruby_) 172
-
- XX. BERYL (_Emerald_, _Aquamarine_, _Morganite_) 184
-
-
- PART II—SECTION B
-
- SEMI-PRECIOUS STONES
-
- XXI. TOPAZ 197
-
- XXII. SPINEL (_Balas-Ruby_, _Rubicelle_) 203
-
- XXIII. GARNET 207
-
- (_a_) HESSONITE (_Grossular_, _Cinnamon-Stone_,
- _Hyacinth_, _Jacinth_) 211
-
- (_b_) PYROPE (‘_Cape-Ruby_’) 212
-
- (_c_) RHODOLITE 214
-
- (_d_) ALMANDINE (_Carbuncle_) 214
-
- (_e_) SPESSARTITE 216
-
- (_f_) ANDRADITE (_Demantoid_, _Topazolite_, ‘_Olivine_’) 216
-
- (_g_) UVAROVITE 218
-
- XXIV. TOURMALINE (_Rubellite_) 219
-
- XXV. PERIDOT 225
-
- XXVI. ZIRCON (_Jargoon_, _Hyacinth_, _Jacinth_) 228
-
- XXVII. CHRYSOBERYL (_Chrysolite_, _Cat’s-Eye_, _Cymophane_,
- _Alexandrite_) 233
-
- XXVIII. QUARTZ (_Rock-Crystal_, _Amethyst_, _Citrine_,
- _Cairngorm_, _Cat’s-Eye_, _Tiger’s-Eye_) 238
-
- XXIX. CHALCEDONY, AGATE, ETC. 246
-
- XXX. OPAL (_White Opal_, _Black Opal_, _Fire-Opal_) 249
-
- XXXI. FELSPAR (_Moonstone_, _Sunstone_, _Labradorite_,
- _Amazon-Stone_) 254
-
- XXXII. TURQUOISE, ODONTOLITE, VARISCITE 257
-
- XXXIII. JADE (NEPHRITE OR GREENSTONE, _Jadeite_) 260
-
- XXXIV. SPODUMENE (_Kunzite_, _Hiddenite_), IOLITE, BENITOITE 265
-
- XXXV. EUCLASE, PHENAKITE, BERYLLONITE 269
-
- XXXVI. ENSTATITE (‘_Green Garnet_’), DIOPSIDE, KYANITE,
- ANDALUSITE, IDOCRASE, EPIDOTE, SPHENE, AXINITE,
- PREHNITE, APATITE, DIOPTASE 271
-
- XXXVII. CASSITERITE, ANATASE, PYRITES, HEMATITE 281
-
- XXXVIII. OBSIDIAN, MOLDAVITE 283
-
-
- PART II—SECTION C
-
- ORNAMENTAL STONES
-
- XXXIX. FLUOR, LAPIS LAZULI, SODALITE, VIOLANE, RHODONITE,
- AZURITE, MALACHITE, THULITE, MARBLE, APOPHYLLITE,
- CHRYSOCOLLA, STEATITE OR SOAPSTONE, MEERSCHAUM,
- SERPENTINE 285
-
-
- PART II—SECTION D
-
- ORGANIC PRODUCTS
-
- XL. PEARL, CORAL, AMBER 291
-
-
- TABLES
-
- I. CHEMICAL COMPOSITION OF GEM-STONES 300
-
- II. COLOUR OF GEM-STONES 301
-
- III. REFRACTIVE INDICES OF GEM-STONES 302
-
- IV. COLOUR-DISPERSION OF GEM-STONES 303
-
- V. CHARACTER OF THE REFRACTION OF GEM-STONES 303
-
- VI. DICHROISM OF GEM-STONES 304
-
- VII. SPECIFIC GRAVITIES OF GEM-STONES 305
-
- VIII. DEGREES OF HARDNESS OF GEM-STONES 305
-
- IX. DATA 306
-
-
- INDEX 307
-
-
-
-
- LIST OF PLATES
-
-
- PAGE
- I. GEM-STONES (in colour) _Frontispiece_
-
- II. REFRACTIVE INDEX DIAGRAM 36
-
- III. INTERFERENCE FIGURES 48
-
- IV. JEWELLERY DESIGNS 62
-
- V. JEWELLERY DESIGNS 88
-
- VI. APPLIANCES USED FOR POLISHING DIAMONDS 102
-
- VII. POLISHING DIAMONDS 103
-
- VIII. SLITTING AND POLISHING COLOURED STONES 104
-
- IX. FACETING MACHINE 105
-
- X. LAPIDARY’S WORKSHOP AND OFFICE IN ENGLAND 106
-
- XI. LAPIDARY’S WORKSHOP IN RUSSIA 107
-
- XII. FRENCH FAMILY CUTTING STONES 108
-
- XIII. INDIAN LAPIDARY 109
-
- XIV. BLOWPIPE USED FOR THE MANUFACTURE OF RUBIES
- AND SAPPHIRES 118
-
- XV. KIMBERLEY MINE, 1871 140
-
- XVI. KIMBERLEY MINE, 1872 141
-
- XVII. KIMBERLEY MINE, 1874 142
-
- XVIII. KIMBERLEY MINE, 1881 143
-
- XIX. KIMBERLEY MINE AT THE PRESENT DAY 144
-
- XX. WESSELTON (open) MINE 145
-
- XXI. LOADING THE BLUE GROUND ON THE FLOORS, AND PLOUGHING IT
- OVER 146
-
- XXII. WASHING-MACHINES FOR CONCENTRATING THE BLUE GROUND 147
-
- XXIII. DIAMOND-SORTING MACHINES 148
-
- XXIV. KAFIRS PICKING OUT DIAMONDS 149
-
- XXV. CULLINAN DIAMOND (natural size) 168
-
- XXVI. LARGE AQUAMARINE CRYSTAL (one-sixth natural size),
- FOUND AT MARAMBAYA, MINAS GERAES, BRAZIL 196
-
- XXVII. GEM-STONES (in colour) 226
-
- XXVIII. OPAL MINES, WHITE CLIFFS, NEW SOUTH WALES 252
-
- XXIX. GEM-STONES (in colour) 256
-
- XXX. NATIVES DRILLING PEARLS 294
-
- XXXI. METAL FIGURES OF BUDDHA INSERTED IN A PEARL-OYSTER 296
-
- XXXII. SECTIONS OF CULTURE PEARL 297
-
-
-
-
- GEM-STONES
-
-
-
-
- CHAPTER I
-
- INTRODUCTION
-
-
-Beauty, durability, and rarity: such are the three cardinal virtues
-of a perfect gem-stone. Stones lacking any of them cannot aspire to
-a high place in the ranks of precious stones, although it does not
-necessarily follow that they are of no use for ornamental purposes. The
-case of pearl, which, though not properly included among gem-stones,
-being directly produced by living agency, yet holds an honoured place
-in jewellery, constitutes to some extent an exception, since its
-incontestable beauty atones for its comparative want of durability.
-
-That a gem-stone should be a delight to the eye is a truism that need
-not be laboured; for such is its whole _raison d’être_. The members
-of the Mineral Kingdom that find service in jewellery may be divided
-into three groups, according as they are transparent, translucent,
-or opaque. Of these the first, which is by far the largest and the
-most important, may itself be further sub-divided into two sections:
-stones which are devoid of colour, and stones which are tinted. Among
-the former, diamond reigns supreme, since it alone possesses that
-marvellous ‘fire,’ oscillating with every movement from heavenly blue
-to glowing red, which is so highly esteemed and so much besought.
-Other stones, such as ‘fired’ zircon, white sapphire, white topaz, and
-rock-crystal, may dazzle with brilliancy of light reflected from the
-surface or emitted from the interior, but none of them, like diamond,
-glow with mysterious gleams. No hint of colour, save perhaps a trace
-of the blue of steel, can be tolerated in stones of this category;
-above all is a touch of the jaundice hue of yellow abhorred. It taxes
-all the skill of the lapidary to assure that the disposition of the
-facets be such as to reveal the full splendour of the stone. A coloured
-stone, on the other hand, depends for its attractiveness more upon its
-intrinsic hue than upon the manner of its cutting. The tint must not be
-too light or too dark in shade: a stone that has barely any colour has
-little interest, and one which is too dark appears almost opaque and
-black. The lapidary can to some extent remedy these defects by cutting
-the former deep and the latter shallow. In certain curious stones—for
-instance tourmaline—the transparency, and in others—such as ruby,
-sapphire, and one of the recent additions to the gem world, kunzite—the
-colour, varies considerably in different directions. The colours that
-are most admired—the fiery red of ruby, the royal blue of sapphire,
-the verdant green of emerald, and the golden yellow of topaz—are pure
-tints, and the absorption spectra corresponding to them are on the
-whole continuous and often restricted. They therefore retain the purity
-of their colour even in artificial light, though certain sapphires
-transmit a relatively larger amount of red, and consequently turn
-purple at night. Of the small group of translucent stones which pass
-light, but are not clear enough to be seen through, the most important
-is opal. It and certain others of the group owe their merit to the
-same optical effect as that characterizing soap-bubbles, tarnished
-steel, and so forth, and not to any intrinsic coloration. Another
-set of stones—moonstone and the star-stones—reflect light from the
-interior more or less regularly, but not in such a way as to produce
-a play of colour. The last group, which comprises opaque stones, has
-a single representative among ordinary gem-stones, namely, turquoise.
-In this case light is scattered and reflected from layers immediately
-contiguous to the surface, and the colour is due to the resulting
-absorption. The apparent darkness of a deep-coloured stone follows from
-a different cause: the light passing into the stone is wholly absorbed
-within it, and, since none is emitted, the stone appears black. The
-claims of turquoise are maintained by the blue variety; there is little
-demand for stones of a greenish tinge.
-
-It is evidently desirable that any stones used in jewellery should be
-able to resist the mechanical and chemical actions of everyday life. No
-one is anxious to replace jewels every few years, and the most valuable
-stones are expected to endure for all time. The mechanical abrasion
-is caused by the minute grains of sand that are contained in ordinary
-dust, and gem-stones should be at least as hard as they—a condition
-fulfilled by all the principal species with the exception of opal,
-turquoise, peridot, and demantoid. Since the beauty of the first named
-does not depend on the brilliancy of its polish, scratches on the
-surface are not of much importance; further, all four are only slightly
-softer than sand. It may be noted that the softness of paste stones,
-apart from any objections that may be felt to the use of imitations,
-renders them unsuitable for jewellery purposes. The only stones that
-are likely to be chemically affected in the course of wear are those
-which are in the slightest degree porous. It is hazardous to immerse
-turquoises in liquids, even in water, lest the bluish green colour be
-oxidized to the despised yellowish hue. The risk of damage to opals,
-moonstones, and star-stones by the penetration of dirt or grease into
-the interior of the stones is less, but is not wholly negligible.
-Similar remarks apply with even greater force to pearls. Their charm,
-which is due to a peculiar surface-play of light, might be destroyed by
-contamination with grease, ink, or similar matter; they are, moreover,
-soft. For both reasons their use in rings is much to be deprecated.
-Nothing can be more unsightly than the dingy appearance of a pearl ring
-after a few years’ wear.
-
-It cannot be gainsaid that mankind prefers the rare to the beautiful,
-and what is within reach of all is lightly esteemed. It is for this
-reason that garnet and moonstone lie under a cloud. Purchasers can
-readily be found for a ‘Cape-ruby’ or an ‘olivine,’ but not for a
-garnet; garnets are so common, is the usual remark. Nevertheless,
-the stones mentioned are really garnets. If science succeeded in
-manufacturing diamonds at the cost of shillings instead of the pounds
-that are now asked for Nature’s products—not that such a prospect is at
-all probable or even feasible—we might expect them to vanish entirely
-from fashionable jewellery.
-
-A careful study of the showcases of the most extensive jewellery
-establishment brings to light the fact that, despite the apparent
-profusion, the number of different species represented is restricted.
-Diamond, ruby, emerald, sapphire, pearl, opal, turquoise, topaz,
-amethyst are all that are ordinarily asked for. Yet, as later pages
-will show, there are many others worthy of consideration; two among
-them—peridot and tourmaline—are, indeed, slowly becoming known. For
-the first five of the stones mentioned above, the demand is relatively
-steady, and varies absolutely only with the purchasing power of the
-world; but a lesser known stone may suddenly spring into prominence
-owing to the caprice of fashion or the preference of some great lady
-or leader of fashion. Not many years ago, for instance, violet was the
-favourite colour for ladies’ dresses, and consequently amethysts were
-much worn to match, but with the change of fashion they speedily sank
-to their former obscurity. Another stone may perhaps figure at some
-royal wedding; for a brief while it becomes the vogue, and afterwards
-is seldom seen.
-
-Except that diamond, ruby, emerald, and sapphire, and, we should add,
-pearl, may indisputably be considered to occupy the first rank, it is
-impossible to form the gem-stones in any strict order. Every generation
-sees some change. The value of a stone is after all merely what it will
-fetch in the open market, and its artistic merits may be a matter of
-opinion. The familiar aphorism, _de gustibus non est disputandum_, is a
-warning not to enlarge upon this point.
-
-
-
-
- PART I—SECTION A
-
- THE CHARACTERS OF GEM-STONES
-
-
-
-
- CHAPTER II
-
- CRYSTALLINE FORM
-
-
-With the single exception of opal, the whole of the principal mineral
-species used in jewellery are distinguished from glass and similar
-substances by one fundamental difference: they are crystallized matter,
-and the atoms composing them are regularly arranged throughout the
-structure.
-
-The words crystal and glass are employed in science in senses differing
-considerably from those in popular use. The former of them is derived
-from the Greek word κρύος, meaning ice, and was at one time used in
-that sense. For instance, the old fourteenth-century reading of Psalm
-cxlvii. 17, which appears in the authorized version as “He giveth his
-ice like morsels,” ran “He sendis his kristall as morcels.” It was
-also applied to the beautiful, lustrous quartz found among the eternal
-snows of the Alps, since, on account of their limpidity, these stones
-were supposed, as Pliny tells us, to consist of water congealed by the
-extreme cold of those regions; such at the present day is the ordinary
-meaning of the word. But, when early investigators discovered that a
-salt solution on evaporation left behind groups of slender glistening
-prisms, each very similar to the rest, they naturally—though, as we
-now know, wrongly—regarded them as representing yet another form
-of congealed water, and applied the same word to such substances.
-Subsequent research has shown that these salts, as well as mineral
-substances occurring with natural faces in nature, have in common the
-fundamental property of regularity of arrangement of the constituent
-atoms, and science therefore defines by the word crystal a substance in
-which the structure is uniform throughout, and all the similar atoms
-composing it are arranged with regard to the structure in a similar way.
-
-The other word is yet more familiar; it denotes the transparent,
-lustrous, hard, and brittle substance produced by the fusion of sand
-with soda or potash or both which fills our windows and serves a
-variety of useful purposes. Research has shown that glass, though
-apparently so uniform in character, has in reality no regularity of
-molecular arrangement. It is, in fact, a kind of mosaic of atoms,
-huddled together anyhow, but so irregular is its irregularity that
-it simulates perfect regularity. Science uses the word glass in this
-widened meaning. Two substances may, as a matter of fact, have the
-same chemical composition, and one be a crystal and the other a glass.
-For example, quartz, if heated to a high temperature, may be fused and
-converted into a glass. The difference in the two types of structure
-may be illustrated by a comparison between a regiment of soldiers
-drawn up on parade and an ordinary crowd of people.
-
-The crystalline form is a visible sign of the molecular arrangement,
-and is intimately associated with the directional physical properties,
-such as the optical characters, cleavage, etc. A study of it is not
-only of interest in itself, but also of great importance to the
-lapidary who wishes to cut a stone to the best advantage, and it is,
-moreover, of service in distinguishing stones when in the rough state.
-
-[Illustration: FIG. 1.—Cubo-Octahedra.]
-
-The development of natural faces on a crystal is far from being
-haphazard, but is governed by the condition that the angles between
-similar faces, whether on the same crystal or on different crystals,
-are equal, however varying may be the shapes and the relative sizes
-of the faces (Fig. 1), and by the tendency of the faces bounding
-the crystal to fall into series with parallel edges, such series
-being termed zones. Each species has a characteristic type of
-crystallization, which may be referred to one of the following six
-systems:—
-
-1. _Cubic._—Crystals in this system can be referred to three edges,
-which are mutually at right angles, and in which the directional
-characters are identical in value. These principal edges are known
-as axes. Some typical forms are the cube (Fig. 2), characteristic
-of fluor; the octahedron (Fig. 3), characteristic of diamond and
-spinel; the dodecahedron (Fig. 4), characteristic of garnet; and the
-triakisoctahedron, or three-faced octahedron (Fig. 5).
-
-[Illustration: FIG. 2.—Cube.]
-
-[Illustration: FIG. 3.—Octahedron.]
-
-[Illustration: FIG. 4.—Dodecahedron.]
-
-All crystals belonging to this system are singly refractive.
-
-2. _Tetragonal._—Such crystals can be referred to three axes, which are
-mutually at right angles, but in only two of them are the directional
-characters identical. A typical form is a four-sided prism, _mm_, of
-square section, terminated by four triangular faces, _p_ (Fig. 6), the
-usual shape of crystals of zircon and idocrase.
-
-[Illustration: FIG. 5.—Triakisoctahedron, or Three-faced Octahedron.]
-
-[Illustration: FIG. 6.—Tetragonal Crystal.]
-
-Crystals belonging to this system are doubly refractive and uniaxial,
-_i.e._ they have one direction of single refraction (cf. p. 45), which
-is parallel to the unequal edge of the three mentioned above.
-
-[Illustration: FIG. 7.—Two alternative sets of Axes in the Hexagonal
-System.]
-
-3. _Hexagonal._—Such crystals can be referred alternatively either
-to a set of three axes, _X_, _Y_, _Z_ (Fig. 7), which lie in a plane
-perpendicular to a fourth, _H_, and are mutually inclined at angles of
-60°, or to a set of three, _a_, _b_, _c_, which are not at right angles
-as in the cubic system, but in which the directional characters are
-identical. The fourth axis in the first arrangement is equally inclined
-to each in the second set of axes. Many important species crystallize
-in this system—corundum (sapphire, ruby), beryl (emerald, aquamarine),
-tourmaline, quartz, and phenakite. The crystals usually display a
-six-sided prism, terminated by a single face, _c_, perpendicular to the
-edge of the prism _m_ (Fig. 8), _e.g._ emerald, or by six or twelve
-inclined faces, _p_ (Fig. 9), _e.g._ quartz, crystals of which are so
-constant in form as to be the most familiar in the Mineral Kingdom.
-Tourmaline crystals (Fig. 10) are peculiar because of the fact that
-often one end is obviously to the eye flatter than the other.
-
-[Illustration: FIGS. 8-10.—Hexagonal Crystals.]
-
-Crystals belonging to this system are also doubly refractive and
-uniaxial, the direction of single refraction being parallel to the
-fourth axis mentioned above, and therefore also parallel to the prism
-edge. Hence deeply coloured tourmaline, which strongly absorbs the
-ordinary ray, must be cut with the table-facet parallel to the edge of
-the prism.
-
-[Illustration: FIG. 11.—Relation of the two directions of single
-Refraction to the Axes in an Orthorhombic Crystal.]
-
-4. _Orthorhombic._—Such crystals can be referred to three axes, which
-are mutually at right angles, but in which each of the directional
-characters are different. The crystals are usually prismatic in shape,
-one of the axes being parallel to the prism edge. Topaz, peridot, and
-chrysoberyl are the most important species crystallizing in this system.
-
-Crystals belonging to this system are doubly refractive and biaxial,
-_i.e._ they have two directions of single refraction (cf. p. 45). The
-three axes _a_, _b_, _c_ (Fig. 11) are parallel respectively to the two
-bisectrices of the directions of single refraction, and the direction
-perpendicular to the plane containing those directions.
-
-5. _Monoclinic._—Such crystals can be referred to three axes, one
-of which is at right angles to the other two, which are, however,
-themselves not at right angles. Spodumene (kunzite) and some moonstone
-crystallize in this system.
-
-Crystals belonging to this system are doubly refractive and biaxial,
-but in this case the first axis alone is parallel to one of the
-principal optical directions.
-
-6. _Triclinic._—Such crystals have no edges at right angles, and the
-optical characters are not immediately related to the crystalline form.
-Some moonstone crystallizes in this system.
-
-[Illustration: FIG. 12.—Twinned Octahedron.]
-
-Crystals are often not single separate individuals. For instance,
-diamond and spinel are found in flat triangular crystals with their
-girdles cleft at the corners (Fig. 12). Each of such crystals is
-really composed of portions of two similar octahedra, which are placed
-together in such a way that each is a reflection of the other. Such
-composite crystals are called twins or macles. Sometimes the twinning
-is repeated, and the individuals may be so minute as to call for a
-microscope for their perception.
-
-A composite structure may also result from the conjunction of
-numberless minute individuals without any definite orientation, as in
-the case of chalcedony and agate. So by supposing the individuals to
-become infinitesimally small, we pass to a glass-like substance.
-
-It is often a peculiarity of crystals of a species to display a typical
-combination of natural faces. Such a combination is known as the habit
-of the species, and is often of service for the purpose of identifying
-stones before they are cut. Thus, a habit of diamond and spinel is
-an octahedron, often twinned, of garnet a dodecahedron, of emerald a
-flat-ended hexagonal prism, and so on.
-
-It is one of the most interesting and remarkable features connected
-with crystallization that the composition and the physical
-characters—for instance, the refractive indices and specific
-gravity—may, without any serious disturbance of the molecular
-arrangement, vary considerably owing to the more or less complete
-replacement of one element by another closely allied to it. That is
-the cause of the range of the physical characters which has been
-observed in such species as tourmaline, peridot, spinel, etc. The
-principal replacements in the case of the gem-stones are ferric oxide,
-Fe_{2}O_{3}, by alumina, Al_{2}O_{3}, and ferrous oxide, FeO, by
-magnesia, MgO.
-
-A list of the principal gem-stones, arranged by their chemical
-composition, is given in Table I at the end of the book.
-
-
-
-
- CHAPTER III
-
- REFLECTION, REFRACTION, AND DISPERSION
-
-
-It is obvious that, since a stone suitable for ornamental use must
-appeal to the eye, its most important characters are those which depend
-upon light; indeed, the whole art of the lapidary consists in shaping
-it in such a way as to show these qualities to the best advantage. To
-understand why certain forms are given to a cut stone, it is essential
-for us to ascertain what becomes of the light which falls upon the
-surface of the stone; further, we shall find that the action of a
-stone upon light is of very great help in distinguishing the different
-species of gem-stones. The phenomena displayed by light which impinges
-upon the surface separating two media[1] are very similar in character,
-whatever be the nature of the media.
-
-Ordinary experience with a plane mirror tells us that, when light is
-returned, or reflected, as it is usually termed, from a plane or flat
-surface, there is no alteration in the size of objects viewed in this
-way, but that the right and the left hands are interchanged: our right
-hand becomes the left hand in our reflection in the mirror. We notice,
-further, that our reflection is apparently just as far distant from the
-mirror on the farther side as we are on this side. In Fig. 13 _MM´_
-is a section of the mirror, and _O´_ is the image of the hand _O_ as
-seen in the mirror. Light from _O_ reaches the eye _E_ by way of _m_,
-but it appears to come from _O´_. Since _OO´_ is perpendicular to the
-mirror, and _O_ and _O´_ lie at equal distances from it, it follows
-from elementary geometry that the angle _i´_, which the reflected ray
-makes with _mn_, the normal to the mirror, is equal to _i_, the angle
-which the incident ray makes with the same direction.
-
-[Illustration: FIG. 13.—Reflection at a Plane Mirror.]
-
-Again, everyday experience tells us that the case is less simple when
-light actually crosses the bounding surface and passes into the other
-medium. Thus, if we look down into a bath filled with water, the
-bottom of the bath appears to have been raised up, and a stick plunged
-into the water seems to be bent just at the surface, except in the
-particular case when it is perfectly upright. Since the stick itself
-has not been bent, light evidently suffers some change in direction as
-it passes into the water or emerges therefrom. The passage of light
-from one medium to another was studied by Snell in the seventeenth
-century, and he enunciated the following laws:—
-
-1. The refracted ray lies in the plane containing the incident ray and
-the normal to the plane surface separating the two media.
-
-It will be noticed that the reflected ray obeys this law also.
-
-2. The angle _r_, which the refracted ray makes with the normal, is
-related to the angle _i_, which the incident ray makes with the same
-direction, by the equation
-
- _n_ sin _i_ = _n´_ sin _r_, (_a_)
-
-where _n_ and _n´_ are constants for the two media which are known as
-the indices of refraction, or the refractive indices.
-
-This simple trigonometrical relation may be expressed in geometrical
-language. Suppose we cut a plane section through the two media at right
-angles to the bounding plane, which then appears as a straight line,
-_SOS´_ (Fig. 14), and suppose that _IO_ represents the direction of
-the incident ray; then Snell’s first law tells us that the refracted
-ray _OR_ will also lie in this plane. Draw the normal _NON´_, and with
-centre _O_ and any radius describe a circle intersecting the incident
-and refracted rays in the points _a_ and _b_ respectively; let drop
-perpendiculars _ac_ and _bd_ on to the normal _NON´_. Then we have
-_n.ac = n´.bd_, whence we see that if _n_ be greater than _n´_, _ac_
-is less than _bd_, and therefore when light passes from one medium
-into another which is less optically dense, in its passage across the
-boundary it is bent, or refracted, away from the normal.
-
-[Illustration: FIG. 14.—Refraction across a Plane Surface.]
-
-We see, then, that when light falls on the boundary of two different
-media, some is reflected in the first and some is refracted into the
-second medium. The relative amounts of light reflected and refracted
-depend on the angle of incidence and the refractive indices of the
-media. We shall return to this point when we come to consider the
-lustre of stones.
-
-We will proceed to consider the course of rays at different angles of
-incidence when light passes out from a medium into one less dense—for
-instance, from water into air. Corresponding to light with a small
-angle of incidence such as _I_{1}O_ (Fig. 15), some of it is reflected
-in the direction _OI´_{1}_ and the remainder is refracted out in the
-direction _OR_{1}_. Similarly, for the ray _I_{2}O_ some is reflected
-along _OI´_{2}_ and some refracted along _OR_{2}_. Since, in the case
-we have taken, the angle of refraction is greater than the angle of
-incidence, the refracted ray corresponding to some incident, ray
-_I_{c}O_ will graze the bounding surface, and corresponding to a
-ray beyond it, such as _I_{3}O_, which has a still greater angle of
-incidence, there is no refracted ray, and all the light is wholly
-or totally reflected within the dense medium. The critical angle
-_I_{c}ON_, which is called the angle of total-reflection, is very
-simply related to the refractive indices of the two media; for, since
-_r_ is now a right angle, sin _r_ = 1, and equation (_a_) becomes
-
- _n_ sin _i_ = _n´_ (_b_)
-
-Hence, if the angle of total-reflection is measured and one of the
-indices is known, the other can easily be calculated.
-
-[Illustration: FIG. 15.—Total-Reflection.]
-
-The phenomenon of total-reflection may be appreciated if we hold a
-glass of water above our head, and view the light of a lamp on a table
-reflected from the under surface of the water. This reflection is
-incomparably more brilliant than that given by the upper surface.
-
-The refractive index of air is taken as unity; strictly, it is that of
-a vacuum, but the difference is too small to be appreciated even in
-very delicate work. Every substance has different indices for light
-of different colour, and it is customary to take as the standard the
-yellow light of a sodium flame. This happens to be the colour to
-which our eyes are most sensitive, and a flame of this kind is easily
-prepared by volatilizing a little bicarbonate of soda in the flame of
-a bunsen burner. A survey of Table III at the end of the book shows
-clearly how valuable a measurement of the refractive index is for
-determining the species to which a cut stone belongs. The values found
-for different specimens of the species do in cases vary considerably
-owing to the great latitude possible in the chemical constitution
-due to the isomorphous replacement of one element by another. Some
-variation in the index may even occur in different directions within
-the same stone; it results from the remarkable property of splitting up
-a beam of light into two beams, which is possessed by many crystallized
-substances. This forms the subject of a later chapter.
-
-Upon the fact that the refractive index of a substance varies for
-light of different colours depends such familiar phenomena as the
-splendour of the rainbow and the ‘fire’ of the diamond. When white
-light is refracted into a stone it no longer remains white, but is
-split up into a spectrum. Except in certain anomalous substances the
-refractive index increases progressively as the wave-length of the
-light decreases, and consequently a normal spectrum is violet at one
-end and passes through green and yellow to red at the other end. The
-width of the spectrum, which may be measured by the difference between
-the refractive indices for the extreme red and violet rays, also
-varies, though on the whole it increases with the refractive index. It
-is the dispersion, as this difference is termed, that determines the
-‘fire’—a character of the utmost importance in colourless transparent
-stones, which, but for it, would be lacking in interest. Diamond excels
-all colourless stones in this respect, although it is closely followed
-by zircon, the colour of which has been driven off by heating; it is,
-however, surpassed by two coloured species: sphene, which is seldom
-seen in jewellery, and demantoid, the green garnet from the Urals,
-which often passes under the misnomer ‘olivine.’ The dispersion of the
-more prominent species for the _B_ and _G_ lines of the solar spectrum
-is given in Table IV at the end of the book.
-
-We will now proceed to discuss methods that may be used for the
-measurement of the refractive indices of cut stones.
-
-
-
-
- CHAPTER IV
-
- MEASUREMENT OF REFRACTIVE INDICES
-
-
-The methods available for the measurement of refractive indices are of
-two kinds, and make use of two different principles. The first, which
-is based upon the very simple relation found in the last chapter to
-subsist at total-reflection, can be used with ease and celerity, and is
-best suited for discriminative purposes; but it is restricted in its
-application. The second, which depends on the measurement of the angle
-between two facets and the minimum deviation experienced by a ray of
-light when traversing a prism formed by them, is more involved, entails
-the use of more elaborate apparatus, and takes considerable time, but
-it is less restricted in its application.
-
-
- (1) THE METHOD OF TOTAL-REFLECTION
-
-We see from equation _b_ (p. 18), connecting the angle of
-total-reflection with the refractive indices of the adjacent media,
-that, if the denser medium be constant, the indices of all less dense
-media may be easily determined from a measurement of the corresponding
-critical angle. In all refractometers the constant medium is a glass
-with a high refractive index. Some instruments have rotatory parts, by
-means of which this angle is actually measured. Such instruments give
-very good results, but suffer from the disadvantages of being neither
-portable nor convenient to handle, and of not giving a result without
-some computation.
-
-[Illustration: FIG. 16.—Refractometer (actual size).]
-
-For use in the identification of cut stones, a refractometer with a
-fixed scale, such as that (Fig. 16) devised by the author, is far
-more convenient. In order to facilitate the observations, a totally
-reflecting prism has been inserted between the two lenses of the
-eyepiece. The eyepiece may be adjusted to suit the individual eyesight;
-but for observers with exceptionally long sight an adapter is provided,
-which permits the eyepiece being drawn out to the requisite extent.
-The refractometer must be held in the manner illustrated in Fig.
-17, so that the light from a window or other source of illumination
-enters the instrument by the lenticular opening underneath. Good,
-even illumination of the field may also very simply be secured by
-reflecting light into the instrument from a sheet of white paper laid
-on a table. On looking down the eyepiece we see a scale (Fig. 18), the
-eyepiece being, if necessary, focused until the divisions of the scale
-are clearly and distinctly seen. Suppose, for experiment, we smear a
-little vaseline or similar fatty substance on the plane surface of the
-dense glass, which just projects beyond the level of the brass plate
-embracing it. The field of view is now no longer uniformly illuminated,
-but is divided into two parts (Fig. 19): a dark portion above, which
-terminates in a curved edge, apparently green in colour, and a bright
-portion underneath, which is composed of totally reflected light. If
-we tilt the instrument downwards so that light enters the instrument
-from above through the vaseline we find that the portions of the field
-are reversed, the dark portion being underneath and terminated by
-a red edge. It is possible so to arrange the illumination that the
-two portions are evenly lighted, and the common edge becomes almost
-invisible. It is therefore essential for obtaining satisfactory results
-that the plate and the dense glass be shielded from the light by the
-disengaged hand. The shadow-edge is curved, and is, indeed, an arc of a
-circle, because spherical surfaces are used in the optical arrangements
-of the refractometer; by the substitution of cylindrical surfaces it
-becomes straight, but sufficient advantage is not secured thereby to
-compensate for the greatly increased complexity of the construction.
-The shadow-edge is coloured, because the relative dispersion,
- _n{v}_ − _n{r}_
- ——————————————— (_n{v}_ and _n{r}_ being the refractive indices for
- _n_
-the extreme violet and red rays respectively), of the vaseline differs
-from that of the dense glass. The dispersion of the glass is very
-high, and exceeds that of any stone for which it can be used. Certain
-oils have, however, nearly the same relative dispersion, and the edges
-corresponding to them are consequently almost colourless. A careful eye
-will perceive that the coloured shadow-edge is in reality a spectrum,
-of which the violet end lies in the dark portion of the field and the
-red edge merges into the bright portion. The yellow colour of a sodium
-flame, which, as has already been stated, is selected as the standard
-for the measurement of refractive indices, lies between the green and
-the red, and the part of the spectrum to be noted is at the bottom of
-the green, and practically, therefore, at the bottom of the shadow,
-because the yellow and red are almost lost in the brightness of the
-lower portion of the field. If a sodium flame be used as the source of
-illumination, the shadow-edge becomes a sharply defined line. The scale
-is so graduated and arranged that the reading where this line crosses
-the scale gives the corresponding refractive index, the reading, since
-the line is curved, being taken in the middle of the field on the
-right-hand side of the scale. The refractometer therefore gives at
-once, without any intermediate calculation, a value of the refractive
-index to the second place of decimals, and a skilled observer
-may, by estimating the tenths of the intervals between successive
-divisions, arrive at the third place; to facilitate this estimation
-the semi-divisions beyond 1·650 have been inserted. The range extends
-nearly to 1·800; for any substance with a higher refractive index the
-field is dark as far as the limit at the bottom.
-
-[Illustration: FIG. 17.—Method of Using the Refractometer.]
-
-[Illustration: FIG. 18.—Scale of the Refractometer.]
-
-[Illustration: FIG. 19.—Shadow-edge given by a singly refractive
-Substance.]
-
-A fat, or a liquid, wets the glass, _i.e._ comes into intimate contact
-with it, but if a solid substance be tested in the same way, a film of
-air would intervene and entirely prevent an observation. To displace
-it, a drop of some liquid which is more highly refractive than the
-substance under test must first be applied to the plane surface
-of the dense glass. The most convenient liquid for the purpose is
-methylene iodide, CH_{2}I_{2}, which, when pure, has at ordinary room
-temperatures a refractive index of 1·742. It is almost colourless when
-fresh, but turns reddish brown on exposure to light. If desired, it
-may be cleared in the manner described below (p. 66), but the film
-of liquid actually used is so thin that this precaution is scarcely
-necessary. If we test a piece of ordinary glass—one of the slips used
-by microscopists for covering thin sections is very convenient for
-the purpose—first applying a drop of methylene iodide to the plane
-surface of the dense glass of the refractometer (Fig. 20), we notice a
-coloured shadow-edge corresponding to the glass-slip at about 1·530 and
-another, almost colourless, at 1·742, which corresponds to the liquid.
-If the solid substance which is tested is more highly refractive than
-methylene iodide, only the latter of the shadow-edges is visible, and
-we must utilize some more refractive liquid. We can, however, raise
-the refractive index of methylene iodide by dissolving sulphur[2] in
-it; the refractive index of the saturated liquid lies well beyond
-1·800 and the shadow-edge corresponding to it, therefore, does not
-come within the range of the refractometer. The pure and the saturated
-liquids can be procured with the instrument, the bottles containing
-them being japanned on the outside to exclude light and fitted with
-dipping-stoppers, by means of which a drop of the liquid required is
-easily transferred to the surface of the glass of the instrument.
-So long as the liquid is more highly refractive than the stone, or
-whatever may be the substance under examination, its precise refractive
-index is of no consequence. The facet used in the test must be flat,
-and must be pressed firmly on the instrument, so that it is truly
-parallel to the plane surface of the dense glass; for good results,
-moreover, it must be bright.
-
-[Illustration: FIG. 20.—Faceted Stone in Position on the Refractometer.]
-
-[Illustration: FIG. 21.—Shadow-edges given by a doubly refractive
-substance.]
-
-We have so far assumed that the substance which we are testing is
-simple and gives a single shadow-edge; but, as may be seen from Table
-V, many of the gem-stones are doubly refractive, and such will,
-in general, show in the field of the refractometer two distinct
-shadow-edges more or less widely separated. Suppose, for example, we
-study the effect produced by a peridot, which displays the phenomenon
-to a marked degree. If we revolve the stone so that the facet under
-observation remains parallel to the plane surface of the dense glass
-of the refractometer and in contact with it, we notice that both the
-shadow-edges in general move up or down the scale. In particular cases,
-depending upon the relation of the position of the facet selected to
-the crystalline symmetry, one or both of them may remain fixed, or
-one may even move across the other. But whatever facet of the stone
-be used for the test, and however variable be the movements of the
-shadow-edges, the highest and lowest readings obtainable remain the
-same; they are the principal indices of refraction, such as are stated
-in Table III at the end of the book, and their difference measures
-the maximum amount of double refraction possessed by the stone. The
-procedure is therefore simplicity itself; we have merely to revolve
-the stone on the instrument, usually through not more than a right
-angle, and note the greatest and least readings. It will be noticed
-that the shadow-edges cross the scale symmetrically in the critical and
-skewwise in intermediate positions. Fig. 21 represents the effect when
-the facet is such as to give simultaneously the two readings required.
-The shadow-edges _a_ and _b_, which are coloured in white light,
-correspond to the least and greatest respectively of the principal
-refractive indices, while the third shadow-edge, which is very faint,
-corresponds to the liquid used—methylene iodide. It is possible, as we
-shall see in a later chapter, to learn from the motion, if any, of the
-shadow-edges something as to the character of the double refraction.
-Since, however, each shadow-edge is spectral in white light, they will
-not be distinctly separate unless the double refraction exceeds the
-relative dispersion. Topaz, for instance, appears in white light to
-yield only a single shadow-edge, and may thus easily be distinguished
-from tourmaline, in which the double refraction is large enough for
-the separation of the two shadow-edges to be clearly discerned. In
-sodium light, however, no difficulty is experienced in distinguishing
-both the shadow-edges given by substances with small amount of double
-refraction, such as chrysoberyl, quartz, and topaz, and a skilled
-observer may detect the separation in the extreme instances of apatite,
-idocrase, and beryl. The shadow-edge corresponding to the greater
-refractive index is always less distinct, because it lies in the bright
-portion of the field. If the stone or its facet be small, it must
-be moved on the plane surface of the dense glass until the greatest
-possible distinctness is imparted to the edge or edges. If it be moved
-towards the observer from the further end, a misty shadow appears to
-move down the scale until the correct position is reached, when the
-edges spring into view.
-
-Any facet of a stone may be utilized so long as it is flat, but the
-table-facet is the most convenient, because it is usually the largest,
-and it is available even when the stone is mounted. That the stone need
-not be removed from its setting is one of the great advantages of this
-method. The smaller the stone the more difficult it is to manipulate;
-caution especially must be exercised that it be not tilted, not only
-because the shadow-edge would be shifted from its true position and an
-erroneous value of the refractive index obtained, but also because a
-corner or edge of the stone would inevitably scratch the glass of the
-instrument, which is far softer than the hard gem-stones. Methylene
-iodide will in time attack and stain the glass, and must therefore be
-wiped off the instrument immediately after use.
-
-
- (2) THE METHOD OF MINIMUM DEVIATION
-
-If the stone be too highly refractive for a measurement of its
-refractive index to be possible with the refractometer just described,
-and it is desired to determine this constant, recourse must be had
-to the prismatic method, for which purpose an instrument known as
-a goniometer[3] is required. Two angles must be measured; one the
-interior angle included between a suitable pair of facets, and the
-other the minimum amount of the deviation produced by the pair upon a
-beam of light traversing them.
-
-[Illustration: FIG. 22.—Path at Minimum Deviation of a Ray traversing a
-Prism formed of two Facets of a Cut Stone.]
-
-Fig. 22 represents a section of a step-cut stone perpendicular to a
-series of facets with parallel edges; _t_ is the table, and _a, b, c_,
-are facets on the culet side. The path of light traversing the prism
-formed by the pair of facets, _t_ and _b_, is indicated. Suppose that
-_A_ is the interior angle of the prism, _i_ the angle of incidence of
-light at the first facet and _i´_ the angle of emergence at the second
-facet, and _r_ and _r´_ the angles inside the stone at the two facets
-respectively. Then at the first facet light has been bent through an
-angle _i - r_, and again at the second facet through an angle _i´ -
-r´_; the angle of deviation, _D_, is therefore given by
-
- _D = i + i´ - (r + r´)_.
-
-We have further that
-
- _r + r´ = A_,
-
-whence it follows that
-
- _A + D = i + i´._
-
-If the stone be mounted on the goniometer and adjusted so that the
-edge of the prism is parallel to the axis of rotation of the instrument
-and if light from the collimator fall upon the table-facet and the
-telescope be turned to the proper position to receive the emergent
-beam, a spectral image of the object-slit, or in the case of a doubly
-refractive stone in general, two spectral images, will be seen in
-white light; in the light of a sodium flame the images will be sharp
-and distinct. Suppose that we rotate the stone in the direction of
-diminishing deviation and simultaneously the telescope so as to retain
-an image in the field of view, we find that the image moves up to and
-then away from a certain position, at which, therefore, the deviation
-is a minimum. The image moves in the same direction from this position
-whichever way the stone be rotated. The question then arises what are
-the angles of incidence and refraction under these special conditions.
-It is clear that a path of light is reversible; that is to say, if a
-beam of light traverses the prism from the facet _t_ to the facet _b_
-it can take precisely the same path from the facet _b_ to the facet
-_t_. Hence we should be led to expect that, since experiment teaches us
-that there is only one position of minimum deviation corresponding to
-the same pair of facets, the angles at the two facets must be equal,
-_i.e._ _i = i´_, and _r = r´_. It is, indeed, not difficult to prove by
-either geometrical or analytical methods that such is the case.
-
- _A_ _A_ + _D_
-Therefore at minimum deviation _r_ = ——— and _i_ = —————————, and,
- 2 2
-since sin _i_ = _n_ sin _r_, where _n_ is the refractive index of
-the stone, we have the simple relation—
- _A_ + _D_
- sin —————————
- 2
- _n_ = —————————————
- _A_
- sin ———
- 2
-
-This relation is strictly true only when the direction of minimum
-deviation is one of crystalline symmetry in the stone, and holds
-therefore in general for all singly refractive stones, and for the
-ordinary ray of a uniaxial stone; but the values thus obtained even in
-the case of biaxial stones are approximate enough for discriminative
-purposes. If then the stone be singly refractive, the result is the
-index required; if it be uniaxial, one value is the ordinary index
-and the other image gives a value lying between the ordinary and the
-extraordinary indices; if it be biaxial, the values given by the two
-images may lie anywhere between the greatest and the least refractive
-indices. The angle _A_ must not be too large; otherwise the light will
-not emerge at the second facet, but will be totally reflected inside
-the stone: on the other hand, it must not be too small, because any
-error in its determination would then seriously affect the accuracy of
-the value derived for the refractive index. Although the monochromatic
-light of a sodium flame is essential for precise work, a sufficiently
-approximate value for discriminative purposes is obtained by noting the
-position of the yellow portion of the spectral image given in white
-light.
-
-In the case of a stone such as that depicted in Fig. 22 images are
-given by other pairs of facets, for instance _ta_ and _tc_, unless the
-angle included by the former is too large. There might therefore be
-some doubt, to which pair some particular image corresponded; but no
-confusion can arise if the following procedure be adopted.
-
-[Illustration: FIG. 23.—Course of Observations in the Method of Minimum
-Deviation.]
-
-The table, or some easily recognizable facet, is selected as the facet
-at which light enters the stone. The telescope is first placed in the
-position in which it is directly opposite the collimator (_T_{0}_ in
-Fig. 23), and clamped. The scale is turned until it reads exactly
-zero, 0° or 360°, and clamped. The telescope is released and revolved
-in the direction of increasing readings of the scale to the position
-of minimum deviation, _T_. The reading of the scale gives at once the
-angle of minimum deviation, _D_. The holder carrying the stone is now
-clamped to the scale, and the telescope is turned to the position,
-_T_{1}_,in which the image given by reflection from the table facet is
-in the centre of the field of view; the reading of the scale is taken.
-The telescope is clamped, and the scale is released and rotated until
-it reads the angle already found for _D_. If no mistake has been made,
-the reflected image from the second facet is now in the field of view.
-It will probably not be quite central, as theoretically it should be,
-because the stone may not have been originally quite in the position
-of minimum deviation, a comparatively large rotation of the stone
-producing no apparent change in the position of the refracted image at
-minimum deviation, and further, because, as has already been stated,
-the method is not strictly true for biaxial stones. The difference in
-readings, however, should not exceed 2°. The reading, _S_, of the scale
-is now taken, and it together with 180° subtracted from the reading for
-the first facet, and the value of _A_, the interior angle between the
-two facets, obtained.
-
-Let us take an example.
-
- Reading _T_ (= _D_) 40° 41´ Reading T_{1} 261° 35´
- less 180° 180 0
- ———————
- 81 35
- Reading _S_ 41 30
- ———————
- ½_D_ 20 20½ _A_ 40 5
- ½_A_ 20 2½ ½_A_ 20 2½
- ———————
- ½(_A_ + _D_) 40 23
-
- Log sin 40° 23´ 9.81151
- Log sin 20 2½ 9.53492
- ———————
- Log _n_ 0.27659
-
- _n_ = 1.8906.
-
-The readings _S_ and _T_ are very nearly the same, and therefore we may
-be sure that no mistake has been made in the selection of the facets.
-
-In place of logarithm-tables we may make use of the diagram on Plate
-II. The radial lines correspond to the angles of minimum deviation and
-the skew lines to the prism angles, and the distance along the radial
-lines gives the refractive index. We run our eye along the line for the
-observed angle of minimum deviation and note where it meets the curve
-for the observed prism angle; the refractive index corresponding to the
-point of intersection is at once read off.
-
-This method has several obvious disadvantages: it requires the use
-of an expensive and elaborate instrument, an observation takes
-considerable time, and the values of the principal refractive indices
-cannot in general be immediately determined.
-
-Table III at the end of the book gives the refractive indices of the
-gem-stones.
-
-[Illustration: _PLATE II_
-
-REFRACTIVE INDEX DIAGRAM]
-
-
-
-
- CHAPTER V
-
- LUSTRE AND SHEEN
-
-
-It has been already stated that whenever light in one medium falls
-upon the surface separating it from another medium some of the light
-is reflected within the first, while the remainder passes out into
-the second medium, except when the first is of lower refractivity
-than the second and light falls at an angle greater than that of
-total-reflection. Similarly, when light impinges upon a cut stone
-some of it is reflected and the remainder passes into the stone. What
-is the relative amount of reflected light depends upon the nature of
-the stone—its refractivity and hardness—and determines its lustre;
-the greater the amount the more lustrous will the stone appear. There
-are different kinds of lustre, and the intensity of each depends on
-the polish of the surface. From a dull, _i.e._ an uneven, surface the
-reflected light is scattered, and there are no brilliant reflections.
-All gem-stones take a good polish, and have therefore, so long as the
-surface retains its polish, considerable brilliancy; turquoise, on
-account of its softness, is always comparatively dull.
-
-The different kinds of lustre are—
-
- (1) Adamantine, characteristic of diamond.
- (2) Vitreous, as seen on the surface of fractured glass.
- (3) Resinous, as shown by resins.
-
-Zircon and demantoid, the green garnet called by jewellers “olivine,”
-alone among gem-stones have a lustre approaching that of diamond. The
-remainder all have a vitreous lustre, though varying in degree, the
-harder and the more refractive species being on the whole the more
-lustrous.
-
-Some stones—for instance, a cinnamon garnet—appear to have a certain
-greasiness in the lustre, which is caused by stray reflections from
-inclusions or other breaks in the homogeneity of the interior. A pearly
-lustre, which arises from cleavage cracks and is typically displayed
-by the cleavage face of topaz, would be seen in a cut stone only when
-flawed.
-
-Certain corundums when viewed in the direction of the
-crystallographical axis display six narrow lines of light radiating at
-angles of 60° from a centre in a manner suggestive of the conventional
-representations of stars. Such stones are consequently known as
-asterias, or more usually star-stones—star-rubies or star-sapphires, as
-the case may be, and the phenomenon is called asterism. These stones
-have not a homogeneous structure, but contain tube-like cavities
-regularly arranged at angles of 60° in planes at right angles to the
-crystallographical axis. The effect is best produced when the stones
-are cut _en cabochon_ perpendicular to that axis.
-
-Chatoyancy is a somewhat similar phenomenon, but in this case the
-fibres or cavities are parallel to a single direction, and a single
-broadish band is displayed at right angles to it. Cat’s-eyes, as these
-stones are termed, are cut _en cabochon_ parallel to the fibres. The
-true cat’s-eye (Plate XXIX, Fig. 1) is a variety of chrysoberyl, but
-the term is also often applied to quartz showing a similar appearance.
-The latter is really a fibrous mineral, such as asbestos, which has
-become converted into silica. The beautiful tiger’s-eye from South
-Africa is a silicified crocidolite, the original blue colour of which
-has been altered by oxidation to golden brown. Recently tourmalines
-have been discovered which are sufficiently fibrous in structure to
-display an effective chatoyancy.
-
-The milky sheen of moonstone (Plate XXIX, Fig. 4) owes its effect to
-reflections from twin lamellæ. The wonderful iridescence which is
-the glory of opal, and is therefore termed opalescence, arises from
-a structure which is peculiar to that species. Opal is a solidified
-jelly; on cooling it has become riddled with extremely thin cracks,
-which were subsequently filled with similar material of slightly
-different refractivity, and thus it consists of a series of films. At
-the surface of each film interference of light takes place just as
-at the surface of a soap-bubble, and the more evenly the films are
-spaced apart the more uniform is the colour displayed, the actual tint
-depending upon the thickness of the films traversed by the light giving
-rise to the phenomenon.
-
-
-
-
- CHAPTER VI
-
- DOUBLE REFRACTION
-
-
-The optical phenomenon presented by many gem-stones is complicated
-by their property of splitting up a beam of light into two with, in
-general, differing characters. In this chapter we shall discuss the
-nature of double refraction, as it is termed, and methods for its
-detection. The phenomenon is not one that comes within the purview of
-everyday experience.
-
-So long ago as 1669 a Danish physician, by name Bartholinus, noticed
-that a plate of the transparent mineral which at that time had
-recently been brought over from Iceland, and was therefore called
-“Iceland-spar,” possessed the remarkable property of giving a double
-image of objects close to it when viewed through it. Subsequent
-investigation has shown that much crystallized matter is doubly
-refractive, but in calcite—to use the scientific name for the species
-which includes Iceland-spar—alone among common minerals is the
-phenomenon so conspicuous as to be obvious to the unaided eye. The
-apparent separation of the pair of images given by a plate cut or
-cleaved in any direction depends upon its thickness. The large mass,
-upwards of two feet (60 cm.) in thickness, which is exhibited at
-the far end of the Mineral Gallery of the British Museum (Natural
-History), displays the separation to a degree that is probably unique.
-
-[Illustration: FIG. 24.—Apparent doubling of the Edges of a Peridot
-when viewed through the Table-Facet.]
-
-Although none of the gem-stones can emulate calcite in this character,
-yet the double refraction of certain of them is large enough to be
-detected without much difficulty. In the case of faceted stones the
-opposite edges should be viewed through the table-facet, and any signs
-of doubling noted. The double refraction of sphene is so large, viz.
-0·08, that the doubling of the edges is evident to the unaided eye.
-In peridot (Fig. 24), zircon (b), and epidote the apparent separation
-of the edges is easily discerned with the assistance of an ordinary
-lens. A keen eye can detect the phenomenon even in the case of such
-substances as quartz with small double refraction. It must, however, be
-remembered that in all such stones the refraction is single in certain
-directions, and the amount of double refraction varies therefore
-with the direction from nil to the maximum possessed by the stone.
-Experiment with a plate of Iceland-spar shows that the rays transmitted
-by it have properties differing from those of ordinary light. On
-superposing a second plate we notice that there are now two pairs of
-images, which are in general no longer of equal brightness, as was the
-case before. If the second plate be rotated with respect to the first,
-two images, one of each pair, disappear, and then the other two, the
-plate having turned through a right angle between the two positions of
-extinction; midway between these positions the images are all equally
-bright. This variation of intensity implies that each of the rays
-emerging from the first plate has acquired a one-sided character, or,
-as it is usually expressed, has become plane-polarized, or, shortly,
-polarized.
-
-[Illustration: FIG. 25.—Wave-Motion.]
-
-Before the discovery of the phenomenon of double refraction the
-foundation of the modern theory of light had been laid by the genius of
-Huygens. According to this theory light is the result of a wave-motion
-(Fig. 25) in the ether, a medium that pervades the whole of space
-whether occupied by matter or not, and transmits the wave-motion at a
-rate varying with the matter with which it happens to coincide. Such
-a medium has been assumed because it explains satisfactorily all the
-phenomena of light, but it by no means follows that it has a concrete
-existence. Indeed, if it has, it is so tenuous as to be imperceptible
-to the most delicate experiments. The wave-motion is similar to that
-observed on the surface of still water when disturbed by a stone flung
-into it. The waves spread out from the source of disturbance; but,
-although the waves seem to advance, the actual particles of water
-merely move up and down, and have no motion at all in the direction
-in which the waves are moving. If we imagine similar motion to take
-place in any plane and not only the horizontal, we form some idea
-of the nature of ordinary light. But after passing through a plate
-of Iceland-spar, light no longer vibrates in all directions, but in
-each beam the vibrations are parallel to a particular plane, the two
-planes being at right angles. The exact relation of the direction of
-the vibrations to the plane of polarization is uncertain, although it
-undoubtedly lies in the plane containing the direction of the ray of
-light and the perpendicular to the plane of polarization. The waves for
-different colours differ in their length, _i.e._ in the distance, 2
-_bb_ (Fig. 25), from crest to crest, while the velocity, which remains
-the same for the same medium, is proportional to the wave-length. The
-intensity of the light varies as the square of the amplitude of the
-wave, _i.e._ the height, _ab_, of the crest from the mean level.
-
-Various methods have been proposed for obtaining polarized light. Thus
-Seebeck found in 1813 that a plate of brown tourmaline cut parallel
-to the crystallographic axis and of sufficient thickness (cf. p. 11)
-transmits only one ray, the other being entirely absorbed within the
-plate. Another method was to employ a glass plate to reflect light at a
-certain critical angle. The most efficient method, and that in general
-use at the present day, is due to the invention of Nicol. A rhomb of
-Iceland-spar (Fig. 26), of suitable length, is sliced along the longer
-diagonal, _dd_, and the halves are cemented together by means of canada
-balsam. One ray, _ioo_, is totally reflected at the surface separating
-the mineral and the cement, and does not penetrate into the other half;
-while the other ray, _iee_, is transmitted with almost undiminished
-intensity. Such a rhomb is called a Nicol’s prism after its inventor,
-or briefly, a nicol.
-
-[Illustration: FIG. 26.—Nicol’s Prism.]
-
-If one nicol be placed above another and their corresponding principal
-planes be at right angles no light is transmitted through the pair.
-In the polarizing microscope one such nicol, called the polarizer, is
-placed below the stage, and the other, called the analyser, is either
-inserted in the body of the microscope or placed above the eyepiece,
-and the pair are usually set in the crossed position so that the field
-of the microscope is dark. If a piece of glass or a fragment of some
-singly refractive substance be placed on the stage the field still
-remains dark; but in case of a doubly refractive stone the field is
-no longer dark except in certain positions of the stone. On rotation
-of the plate, or, if possible, of the nicols together, the field
-passes from darkness to maximum brightness four times in a complete
-revolution, the relative angular intervals between these positions
-being right angles. These positions of darkness are known as the
-positions of extinction, and the plate is said to extinguish in them.
-This test is exceedingly delicate and reveals the double refraction
-even when the greatest difference in the refractive indices is too
-small to be measured directly.
-
-Doubly refractive substances are of two kinds: uniaxial, in which
-there is one direction of single refraction, and biaxial, in which
-there are two such directions. In the case of the former the direction
-of one, the ordinary ray, is precisely the same as if the refraction
-were single, but the refractive index of the other ray varies from
-that of the ordinary ray to a second limiting value, the extraordinary
-refractive index, which may be either greater or less. If the
-extraordinary is greater than the ordinary refractive index the double
-refraction is said to be positive; if less, to be negative. A biaxial
-substance is more complex. It possesses three principal directions,
-viz., the bisectrices of the directions of single refraction and the
-perpendicular to the plane containing them. The first two correspond
-to the greatest and least, and the last to the mean of the principal
-indices of refraction. If the acute bisectrix corresponds to the
-least refractive index, the double refraction is said to be positive,
-and if to the greatest, negative. The relation of the directions of
-single refraction, _s_, to the three principal directions, _a, b, c_,
-is illustrated in Fig. 27 for the case of topaz, a positive mineral.
-The refractive indices of the rays traversing one of the principal
-directions have the values corresponding to the other two. In the
-direction _a_ we should measure the greatest and the mean of the
-principal refractive indices, in the direction _b_ the greatest and the
-least, and in the direction _c_ the mean and the least. The maximum
-amount of double refraction is therefore in the direction _b_.
-
-[Illustration: FIG. 27.—Relation of the two Directions of single
-Refraction to the principal Optical Directions in a Biaxial Crystal.]
-
-In the examination of a faceted stone, of the most usual shape, the
-simplest method is to lay the large facet, called the table, on a glass
-slip and view the stone through the small parallel facet, the culet.
-Should the latter not exist, it may frequently happen that owing to
-internal reflection no light emerges through the steeply inclined
-facets. This difficulty is easily overcome by immersing the stone in
-some highly refracting oil. A glass plate held by hand over the stone
-with a drop of the oil between it and the plate serves the purpose, and
-is perhaps a more convenient method. A stone which does not possess a
-pair of parallel facets should be viewed through any pair which are
-nearly parallel.
-
-We have stated that a plate of glass has no effect on the field.
-Suppose, however, it were viewed when placed between the jaws of a
-tightened vice and thus thrown into a state of strain, it would then
-show double refraction, the amount of which would depend on the strain.
-Natural singly refractive substances frequently show phenomena of a
-similar kind. Thus diamond sometimes contains a drop of liquid carbonic
-acid, and the strain is revealed by the coloured rings surrounding
-the cavity which are seen when the stone is viewed between crossed
-nicols. Double refraction is also common in diamond even when there is
-no included matter to explain it, and is caused by the state of strain
-into which the mineral is thrown on release from the enormous pressure
-under which it was formed. Other minerals which display these so-called
-optical anomalies, such as fluor and garnet, are not really quite
-singly refractive at ordinary temperatures; each crystal is composed
-of several double refractive individuals. But all such phenomena
-cannot be confused with the characters of minerals which extinguish
-in the ordinary way, since the stone will extinguish in small patches
-and these will not be dark all at the same time; further, the double
-refraction is small, and on revolving the stone between crossed nicols
-the extinction is not sharp. Paste stones are sometimes in a state of
-strain, and display slight, but general, double refraction. Hence the
-existence of double refraction does not necessarily prove that the
-stone is real and not an imitation. Stones may be composed of two or
-more individuals which are related to each other by twinning, in which
-case each individual would in general extinguish separately. Such
-individuals would be larger and would extinguish more sharply than the
-patches of an anomalous stone.
-
-[Illustration: FIG. 28.—Interference of Light.]
-
-An examination in convergent light is sometimes of service. An
-auxiliary lens is placed over the condenser so as to converge the light
-on to the stone. Light now traverses the stone in different directions;
-the more oblique the direction the greater the distance traversed in
-the stone. If it be doubly refractive, in any given direction there
-will be in general two rays with differing refractive indices and the
-resulting effect is akin to the well-known phenomenon of Newton’s
-rings, and is an instance of what is termed interference. It may be
-mentioned that the interference of light (Fig. 28) explains such common
-phenomena as the colours of a soap-bubble, the hues of tarnished steel,
-the tints of a layer of oil floating on water, and so on. Light, after
-diverging from the stone, comes to focus a little beneath the plane
-in which the image of the stone is formed. An auxiliary lens must,
-therefore, be inserted to bring the focal planes together, so that the
-interference picture may be viewed by means of the same eyepiece.
-
-If a uniaxial crystal be examined along the crystallographic axis in
-convergent light an interference picture will be seen of the kind
-illustrated on Plate III. The arms of a black cross meet in the centre
-of the field, which is surrounded by a series of circular rings,
-coloured in white light. Rotation of the stone about the axis
-produces no change in the picture.
-
-[Illustration: _PLATE III_
-
-1. UNIAXIAL
-
-2. UNIAXIAL (_Circular Polarization_)
-
-3. BIAXIAL (_Crossed Brushes_)
-
-4. BIAXIAL (_Hyperbolic Brushes_)
-
-INTERFERENCE FIGURES]
-
-A biaxial substance possesses two directions (_the optic axes_) along
-which a single beam is transmitted. If such a stone be examined along
-the line bisecting the acute angle between the optic axes (_the acute
-bisectrix_) an interference picture[4] will be seen which in particular
-positions of the stone with respect to the crossed nicols takes the
-forms illustrated on Plate III. As before, there is a series of rings
-which are coloured in white light; they, however, are no longer circles
-but consist of curves known as lemniscates, of which the figure of 8
-is a special form. Instead of an unchangeable cross there are a pair
-of black “brushes” which in one position of the stone are hyperbolæ,
-and in that at right angles become a cross. On rotating the stone we
-find that the rings move with it and are unaltered in form, whereas the
-brushes revolve about two points, called the “eyes,” where the optic
-axes emerge. If the observation were made along the obtuse bisectrix
-the angle between the optic axes would probably be too large for the
-brushes to come into the field, and the rings might not be visible in
-white light, though they would appear in monochromatic light. In the
-case of a substance like sphene the figure is not so simple, because
-the positions of the optic axes vary greatly for the different colours
-and the result is exceedingly complex; in monochromatic light, however,
-the usual figure is visible.
-
-It would probably not be possible in the case of a faceted stone
-to find a pair of faces perpendicular to the required direction.
-Nevertheless, so long as a portion of the figures described is in the
-field of view, the character of the double refraction, whether uniaxial
-or biaxial, may readily be determined.
-
-There is yet another remarkable phenomenon which must not be passed
-over. Certain substances, of which quartz is a conspicuous example and
-in this respect unique among the gem-stones, possess the remarkable
-property of rotating the plane of polarization of a ray of light which
-is transmitted parallel to the optic axis. If a plate of quartz be
-cut at right angles to the axis and placed between crossed nicols in
-white light, the field will be coloured, the hue changing on rotation
-of one nicol with respect to the other. Examination in monochromatic
-light shows that the field will become dark after a certain rotation of
-the one nicol with respect to the other, the amount of which depends
-on the thickness of the plate. If the plate be viewed in convergent
-light, an interference picture is seen as illustrated on Plate III,
-which is similar to, and yet differs in some important particulars
-from the ordinary interference picture of a uniaxial stone. The cross
-does not penetrate beyond the innermost ring and the centre of the
-field is coloured in white light. If a stone shows such a picture, it
-may be safely assumed to be quartz. It is interesting to note that
-minerals which possess this property have a spiral arrangement of the
-constituent atoms.
-
-It has already been remarked (p. 28) that if a faceted doubly
-refractive stone be rotated with one facet always in contact with the
-dense glass of the refractometer the pair of shadow-edges that are
-visible in the field move up or down the scale in general from or
-to maximum and minimum positions. The manner in which this movement
-takes place depends upon the character of the double refraction and
-the position of the facet under observation with regard to the optical
-symmetry of the stone. In the case of a uniaxial stone, if the facet
-be perpendicular to the crystallographic axis, i.e. the direction
-of single refraction, neither of the shadow-edges will move. If the
-facet be parallel to that direction, one shadow-edge will move up and
-coincide with the other, which remains invariable in position, and
-away from it to a second critical position; the latter gives the value
-of the extraordinary refractive index, and the invariable shadow-edge
-corresponds to the ordinary refractive index. This phenomenon is
-displayed by the table-facet of most tourmalines, because for
-reasons given above (p. 11) they are as a rule cut parallel to the
-crystallographic axis. In the case of facets in intermediate positions,
-the shadow-edge corresponding to the extraordinary refractive index
-moves, but not to coincidence with the invariable shadow-edge. The case
-of a biaxial stone is more complex. If the facet be perpendicular to
-one of the principal directions one shadow-edge remains invariable in
-position, corresponding to one of the principal refractive indices,
-whilst the other moves between the critical values corresponding
-to the remaining two of the principal refractive indices. In the
-interesting case in which the facet is parallel to the two directions
-of single refraction, the second shadow-edge moves across the one which
-is invariable in position. In intermediate positions of the facet
-both shadow-edges move, and give therefore critical values. Of the
-intermediate pair, _i.e._ the lower maximum and the higher minimum,
-one corresponds to the mean principal refractive index, and the other
-depends upon the relation of the facet to the optical symmetry. If it
-is desired to distinguish between them, observations must be made on
-a second facet; but for discriminative purposes such exactitude is
-unnecessary, since the least and the greatest refractive indices are
-all that are required.
-
-The character of the refraction of gem-stones is given in Table V at
-the end of the book.
-
-
-
-
- CHAPTER VII
-
- ABSORPTION EFFECTS: COLOUR, DICHROISM, ETC.
-
-
-When white light passes through a cut stone, colour effects result
-which arise from a variety of causes. The most obvious is the
-fundamental colour of the stone, which is due to its selective
-absorption of the light passing through it, and would characterize
-it before it was cut. Intermingled with the colour in a transparent
-stone is the dispersive effect known as ‘fire,’ which has already
-been discussed (p. 20). In many instances the want of homogeneity is
-responsible for some peculiar effects such as opalescence, chatoyancy,
-and asterism. These phenomena will now be considered in fuller detail.
-
-
- COLOUR
-
-All substances absorb light to some extent. If the action is slight and
-affects equally the whole of the visible spectrum, the stone appears
-white or colourless. Usually some portion is more strongly absorbed
-than the rest, and the stone seems to be coloured. What is the precise
-tint depends not only upon the portions transmitted through the stone,
-but also upon their relative intensities. The eye, unlike the ear, has
-not the power of analysis and it cannot of itself determine how a
-composite colour has been made up. Indeed, so far as it is concerned,
-any colour may be exactly matched by compounding in certain proportions
-three simple primary colours—red, yellow, and violet. Alexandrite, a
-variety of chrysoberyl, is a curious and instructive case. The balance
-in the spectrum of light transmitted through it is such that, whereas
-in daylight such stones appear green, in artificial light, especially
-in gas-light, they are a pronounced raspberry-red (Plate XXVII,
-Figs. 11, 13). The phenomenon is intensified by the strong dichroism
-characteristic of this species.
-
-The colour is the least reliable character that may be employed for the
-identification of a stone, since it varies considerably in the same
-species, and often results from the admixture of some metallic oxide,
-which has no essential part in the chemical composition and is present
-in such minute quantities as to be almost imperceptible by analysis.
-Who would, for instance, imagine from their appearance that stones so
-markedly diverse in hue as ruby and sapphire were really varieties of
-the same species, corundum? Again, quartz, in spite of the simplicity
-of its composition, displays extreme differences of tint. Nevertheless,
-certain varieties do possess a distinctive colour, emerald being
-the most striking example, and in other cases the trained eye can
-appreciate certain characteristic subtleties of shade. At any rate, the
-colour is the most obvious of the physical characters, and serves to
-provide a rough division of the species, and accordingly in Table II at
-the end of the book the gem-stones are arranged by their usual tints.
-
-
- DICHROISM
-
-The two rays into which a doubly refractive stone splits up a ray of
-light are often differently absorbed by it, and in consequence appear
-on emergence differently coloured; such stones are said to be dichroic.
-The most striking instance is a deep-brown tourmaline, which, except
-in very thin sections, is quite opaque to the ordinary ray. The light
-transmitted by a plate cut parallel to the crystallographic axis is
-therefore plane-polarized; before the invention by Nicol of the prism
-of Iceland-spar known by his name this was the ordinary method of
-obtaining light of this character (cf. p. 43). Again, in the case of
-kunzite and cordierite the difference in colour is so marked as to be
-obvious to the unaided eye; but where the contrast is less pronounced
-we require the use of an instrument called a dichroscope, which enables
-the twin colours to be seen side by side.
-
-[Illustration: FIG. 29.—Dichroscope (actual size).]
-
-[Illustration: FIG. 30.—Field of the Dichroscope.]
-
-Fig. 29 illustrates in section the construction of a dichroscope. The
-instrument consists essentially of a rhomb of Iceland-spar, _S_, of
-such a length as to give two contiguous images (Fig. 30) of a square
-hole, _H_, in one end of the tube containing it. In some instruments
-the terminal faces of the rhomb are ground at right angles to its
-length, but usually, as in that depicted, prisms of glass, _G_, are
-cemented on to the two ends. A cap _C_, with a slightly larger hole,
-which is circular in shape, fits on the end of the tube, and can be
-moved up and down it and revolved round it, as desired. The stone, _R_,
-to be tested may be directly attached to it by means of some kind of
-wax or cement in such a way that light which has traversed it passes
-into the window, _H_, of the instrument; the cap at the same time
-permits of the rotation of the stone about the axis of the main tube of
-the instrument. The dichroscope shown in the figure has a still more
-convenient arrangement: it is provided with an additional attachment,
-_A_, by means of which the stone can be turned about an axis at right
-angles to the length of the tube, and thus examined in different
-directions. At the other end of the main tube is placed a lens, _L_, of
-low power for viewing the twin images: the short tube containing it can
-be pushed in and out for focusing purposes. Many makers now place the
-rhomb close to the lens, _L_, and thereby require a much smaller piece
-of spar; material suitable for optical purposes is fast growing scarce.
-
-Suppose that a plate of tourmaline cut parallel to its crystallographic
-axis is fastened to the cap and the latter rotated. We should notice,
-on looking through the instrument, that in the course of a complete
-revolution there are two positions, orientated at right angles to
-one another, in which the tints of the two images are identical, the
-positions of greatest contrast of tint being midway between. If we
-examine a uniaxial stone in a direction at right angles to its optic
-axis we obtain the colours corresponding to the ordinary and the
-extraordinary rays. In any direction less inclined to the axis we
-still have the colour for the ordinary ray, but the other colour is
-intermediate in tint between it and that for the extraordinary ray.
-The phenomenon presented by a biaxial stone is more complex. There
-are three principal colours which are visible in differing pairs in
-the three principal optical directions; in other directions the tints
-seen are intermediate between the principal colours. Since biaxial
-stones have three principal colours, they are sometimes said to be
-trichroic or pleochroic, but in any single direction they have two
-twin colours and show dichroism. No difference at all will be shown in
-directions in which a stone is singly refractive, and it is therefore
-always advisable to examine a stone in more than one direction lest
-the first happens to be one of single refraction. For determinative
-purposes it is not necessary to note the exact shades of tint of the
-twin colours, because they vary with the inherent colour of the stone,
-and are therefore not constant for the same species; we need only
-observe, when the stone is tested with the dichroscope, whether there
-is any variation of colour, and, if so, its strength. Dichroism is a
-result of double refraction, and cannot exist in a singly refractive
-stone. The converse, however, is not true and it by no means follows
-that, because no dichroism can be detected in a stone, it is singly
-refractive. A colourless stone, for instance, cannot possibly be
-dichroic, and many coloured, doubly refractive stones—for example,
-zircon—exhibit no dichroism, or so little that it is imperceptible.
-The character is always the better displayed, the deeper the inherent
-colour of the stone. The deep-green alexandrite, for instance, is far
-more dichroic than the lighter coloured varieties of chrysoberyl.
-
-If the stone is attached to the cap of the instrument, the table should
-be turned towards it so as to assure that the light passing into the
-instrument has actually traversed the stone. If little light enters
-through the opposite coign, a drop of oil placed thereon will overcome
-the difficulty (cf. p. 46). It is also necessary, for reasons mentioned
-above, to examine the stone in directions as far as possible across
-the girdle also. A convenient, though not strictly accurate, method
-is to lay the stone with the table facet on a table and examine the
-light which has entered the stone and been reflected at that facet. The
-stone may easily be rotated on the table, and observations thus made
-in different directions in the stone. Care must be exercised in the
-case of a faceted stone not to mistake the alteration in colour due to
-dispersion for a dichroic effect, and the stone must be placed close to
-the instrument during an observation, because otherwise the twin rays
-traversing the instrument may have taken sensibly different directions
-in the stone.
-
-Dichroism is an effective test in the case of ruby; its twin
-colours—purplish and yellowish red—are in marked contrast, and readily
-distinguish it from other red stones. Again, one of the twin colours
-of sapphire is distinctly more yellowish than the other; the blue
-spinel, of which a good many have been manufactured during recent
-years, is singly refractive, and, of course, shows no difference of
-tint in the dichroscope.
-
-Table VI at the end of the book gives the strength of the dichroism of
-the gem-stones.
-
-
- ABSORPTION SPECTRA
-
-A study of the chromatic character of the light transmitted by a
-coloured stone is of no little interest. As was stated above, the eye
-has not the power of analysing light, and to resolve the transmitted
-rays into their component parts an instrument known as a spectroscope
-is needed. The small ‘direct-vision’ type has ample dispersion for this
-purpose. It is advantageous to employ by preference the diffraction
-rather than the prism form, because in the former the intervals in the
-resulting spectrum corresponding to equal differences of wave-length
-are the same, whereas in the latter they diminish as the wave-length
-increases and accordingly the red end of the spectrum is relatively
-cramped.
-
-The absorptive properties of all doubly refractive coloured substances
-vary more or less with the direction in which light traverses them
-according to the amount of dichroism that they possess, but the
-variation is not very noticeable unless the stone is highly dichroic.
-If the light transmitted by a deep-coloured ruby be examined with a
-spectroscope it will be found that the whole of the green portion of
-the spectrum is obliterated (Fig. 31), while in the case of a sapphire
-only a small portion of the red end of the spectrum is absorbed.
-Alexandrite affords especial interest. In the spectrum of the light
-transmitted by it, the violet and the yellow are more or less strongly
-absorbed, depending upon the direction in which the rays have passed
-through the stone (Fig. 31), and the transmitted light is mainly
-composed of two portions—red and green. The apparent colour of the
-stone depends, therefore, upon which of the two predominates. In
-daylight the resultant colour is green flecked with red and orange,
-the three principal absorptive tints (cf. p. 235), but in artificial
-light, which is relatively stronger in the red portion of the spectrum,
-the resultant colour is a raspberry-red, and there is less apparent
-difference in the absorptive tints (cf. Plate XXVII, Figs. 11, 13).
-
-[Illustration: FIG. 31.—Absorption Spectra.]
-
-In all the spectra just considered, and in all like them, the portions
-that are absorbed are wide, the passage from blackness to colour is
-gradual, and the edges deliminating them are blurred. In the spectra of
-certain zircons and in almandine garnet the absorbed portions, or bands
-as they are called, are narrow, and, moreover, the transition from
-blackness to colour is sharp and abrupt; such stones are therefore said
-to display absorption-bands. Church in 1866 was the first to notice
-the bands shown by zircon (Fig. 31). Sorby thought they portended the
-existence of a new element, to which he gave the name jargonium, but
-subsequently discovered that they were caused by the presence of a
-minute trace of uranium. A yellowish-green zircon shows the phenomenon
-best, and it has all the bands shown in the figure. The spectrum varies
-slightly but almost imperceptibly with the direction in the stone.
-Others show the bands in the yellow and green, while others show only
-those in the red, and some only one of them. The bands are not confined
-to stones of any particular colour, or amount of double refraction.
-Again, many zircons show no bands at all, so that their absence by no
-means precludes the stone from being a zircon.
-
-Almandine is characterized by a different spectrum (Fig. 31). The band
-in the yellow is the most conspicuous, and is no doubt responsible for
-the purple hue of a typical almandine. The spectrum varies in strength
-in different stones. Rhodolite (p. 214), a garnet lying between
-almandine and pyrope, displays the same bands, and indications of them
-may be detected in the spectra of pyropes of high refraction.
-
-[Illustration: _PLATE IV_
-
-JEWELLERY DESIGNS]
-
-
-
-
- CHAPTER VIII
-
- SPECIFIC GRAVITY
-
-
-It is one of our earliest experiences that different substances of
-the same size have often markedly different weights; thus, there is
-a great difference between wood and iron, and still greater between
-wood and lead. It is usual to say that iron is heavier than wood,
-but the statement is misleading, because it would be possible by
-selecting a large enough piece of wood to find one at least as heavy
-as a particular piece of iron. We have, in fact, to compare equal
-volumes of the two substances, and all ambiguity is removed if we
-speak of relative density or specific gravity—the former term being
-usually applied to liquids and the latter to solids—instead of weight
-or heaviness. The density of water at 4° C. is taken as unity, that
-being the temperature at which it is highest; at other temperatures it
-is somewhat lower, as will be seen from Table IX given at the end of
-the book. The direct determination of the volume of an irregular solid
-presents almost insuperable difficulty; but, fortunately, for finding
-the specific gravity it is quite unnecessary to know the volume, as
-will be shown when we proceed to consider the methods in use.
-
-The specific gravity of a stone is a character which is within narrow
-limits constant for each species, and is therefore very useful for
-discriminative purposes. It can be determined whatever be the shape
-of the stone, and it is immaterial whether it be transparent or not;
-but, on the other hand, the stone must be unmounted and free from the
-setting.
-
-The methods for the determination of the specific gravity are of two
-kinds: in the first a liquid is found of the same, or nearly the same,
-density as the stone, and in the second weighings are made and the use
-of an accurate balance is required.
-
-
- (1) HEAVY LIQUIDS
-
-Experiment tells us that a solid substance floats in a liquid denser
-than itself, sinks in one less dense, and remains suspended at any
-level in one of precisely the same density. If the stone be only
-slightly less dense than the liquid, it will rise to the surface; if
-it be just as slightly denser, it will as surely sink to the bottom,
-a physical fact which has added so much to the difficulty and danger
-of submarine manœuvring. If then we can find a liquid denser than the
-stone to be tested, and place the latter in it, the stone will float on
-the surface. If we take a liquid which is less dense than the stone and
-capable of mixing with the heavier liquid, and add it to the latter,
-drop by drop, gently stirring so as to assure that the density of
-the combination is uniformly the same throughout, a stage is finally
-reached when the stone begins to move downwards. It has now very nearly
-the density of the liquid, and, if we find by some means this density,
-we know simultaneously the specific gravity of the stone.
-
-Various devices and methods are available for ascertaining the density
-of liquids—for instance, Westphal’s balance; but, apart from the
-inconvenience attending such a determination, the density of all
-liquids is somewhat seriously affected by changes in the temperature,
-and it is therefore better to make direct comparison with fragments
-of substances of known specific gravity, which are termed indicators.
-If of two fragments differing slightly in specific gravity one floats
-on the surface of a uniform column of liquid and the other lies at
-the bottom of the tube containing the liquid, we may be certain that
-the density of the liquid is intermediate between the two specific
-gravities. Such a precaution is necessary because, if the liquid be a
-mixture of two distinct liquids, the density would tend to increase
-owing to the greater volatility of the lighter of them, and in any case
-the density is affected by change of temperature. The specific gravity
-of stones is not much altered by variation in the temperature.
-
-A more convenient variation of this method is to form a diffusion
-column, so that the density increases progressively with the depth.
-If the stone under test floats at a certain level in such a column
-intermediate between two fragments of known specific gravity, its
-specific gravity may be found by elementary interpolation. To form a
-column of this kind the lighter liquid should be poured on to the top
-of the heavier. Natural diffusion gives the most perfect column, but,
-being a lengthy process, it may conveniently be quickened by gently
-shaking the tube, and the column thus formed gives results sufficiently
-accurate for discriminative purposes.
-
-By far the most convenient liquid for ordinary use is methylene
-iodide, which has already been recommended for its high refraction.
-It has, when pure, a density at ordinary room-temperatures of 3·324,
-and it is miscible in all proportions with benzol, whose density is
-O·88, or toluol, another hydrocarbon which is somewhat less volatile
-than benzol, and whose density is about the same, namely, 0·86. When
-fresh, methylene iodide has only a slight tinge of yellow, but it
-rapidly darkens on exposure to light owing to the liberation of iodine
-which is in a colloidal form and cannot be removed by filtration.
-The liquid may, however, be easily cleared by shaking it up with any
-substance with which the iodine combines to form an iodide removable
-by filtration. Copper filings answer the purpose well, though rather
-slow in action; mercury may also be used, but is not very satisfactory,
-because a small amount may be dissolved and afterwards be precipitated
-on to the stone under test, carrying it down to the bottom of the tube.
-Caustic potash (potassium hydroxide) is also recommended; in this case
-the operation should preferably be carried out in a special apparatus
-which permits the clear liquid to be drawn off underneath, because
-water separates out and floats on the surface. In Fig. 32 three cut
-stones, a quartz (_a_), a beryl (_b_), and a tourmaline (_c_) are shown
-floating in a diffusion column of methylene iodide and benzol. Although
-the beryl is only slightly denser than the quartz, it floats at a
-perceptibly lower level. These three species are occasionally found as
-yellow stones of very similar tint.
-
-[Illustration: FIG. 32.—Stones of different Specific Gravities floating
-in a Diffusion Column of heavy Liquid.]
-
-Various other liquids have been used or proposed for the same
-purpose, of which two may be mentioned. The first of them is a
-saturated solution of potassium iodide and mercuric iodide in water,
-which is known after the discoverer as Sonstadt’s solution. It is a
-clear mobile liquid with an amber colour, having at 12° C. a density
-of 3·085; it may be mixed with water to any extent, and is easily
-concentrated by heating; moreover, it is durable and not subject to
-alteration of any kind; on the other hand, it is highly poisonous and
-cauterizes the skin, not being checked by albumen; it also destroys
-brass-ware by amalgamating the metal. The second is Klein’s solution,
-a clear yellow liquid which has at 15° C. a density of 3·28. It
-consists of the boro-tungstate of cadmium, of which the formula is
-9WO_{3}.B_{2}O_{3}.2CdO.2H_{2}O + 16Aq, dissolved in water, with which
-it may be diluted. If the salt be heated, it fuses at 75° C. in its
-own water of crystallization to a yellow liquid, very mobile, with a
-density of 3·55. Klein’s solution is harmless, but it cannot compare
-for convenience of manipulation with methylene iodide.
-
-The most convenient procedure is to have at hand three glass tubes,
-fitted with stoppers or corks, to contain liquids of different
-densities—
-
-(_a_) Methylene iodide reduced to 2·7; using as indicators orthoclase
-2·55, quartz 2·66, and beryl 2·74.
-
-(_b_) Methylene iodide reduced to 3·1; indicators, beryl 2·74 and
-tourmaline 3·10.
-
-(_c_) Methylene iodide, undiluted, 3·32.
-
-The pure liquid in the last tube should on no account be diluted; but
-the density of the other two liquids may be varied slightly, either
-by adding benzol in order to lower it, or by allowing benzol, which
-has far greater volatility than methylene iodide, to evaporate, or by
-adding methylene iodide, in order to increase it. The density of the
-liquids may be ascertained approximately from the indicators.
-
-A glance at the table of specific gravities shows that as regards the
-gem-stones methylene iodide is restricted in its application, since
-it can be used to test only moonstone, quartz, beryl, tourmaline, and
-spodumene; opal and turquoise, being amorphous and more or less porous,
-should not be immersed in liquids, lest the appearance of the stone be
-irretrievably injured. Methylene iodide readily serves to distinguish
-the yellow quartz from the true topaz, with which jewellers often
-confuse it, the latter stone sinking in the liquid; again aquamarine
-floats, but the blue topaz, which is often very similar to it, sinks in
-methylene iodide.
-
-By saturating methylene iodide with iodine and iodoform, we have a
-liquid (_d_) of density 3·6; a fragment of topaz, 3·55, may be used to
-indicate whether the liquid has the requisite density. Unfortunately
-this saturated solution is so dark as to be almost opaque, and is,
-moreover, very viscous. Its principal use is to distinguish diamond,
-3·535, from the brilliant colourless zircon, with which, apart from
-a test for hardness, it may easily be confused. It is easy to see
-whether the stone floats, as it would do if a diamond. To recover a
-stone which has sunk, the only course is to pour off the liquid into
-another tube, because it is far too dark for the position of the stone
-to be seen.
-
-It is possible to employ a similar method for still denser stones by
-having recourse to Retgers’s salt, silver-thallium nitrate. This double
-salt is solid at ordinary room-temperatures, but has the remarkable
-property of melting at a temperature, 75° C., which is well below the
-point of fusion of either of its constituents, to a clear, mobile
-yellow liquid, which is miscible in any proportion with water, and
-has, when pure, a density of 4·6. The salt may be purchased, or it may
-be prepared by mixing 100 grams of thallium nitrate and 64 grams of
-silver nitrate, or similar proportions, in a little water, and heating
-the whole over a water-bath, keeping it constantly stirred with a
-glass rod until it is liquefied. The two salts must be mixed in the
-correct proportions, because otherwise the mixture might form other
-double salts, which do not melt at so low a temperature. A glance at
-the table of specific gravities shows that Retgers’s salt may be used
-for all the gem-stones with the single exception of zircon (b). There
-are, however, some objections to its use. It is expensive, and, unless
-kept constantly melted, it is not immediately available. It darkens on
-exposure to strong sunlight like all silver salts, stains the skin a
-peculiar shade of purple which is with difficulty removed, and in fact
-only by abrasion of the skin, and, like all thallium compounds, is
-highly poisonous.
-
-It is convenient to have three tubes, fitted as before with stoppers
-or corks, to contain the following liquids, when heated:—
-
-(_e_) Silver-thallium nitrate, reduced to 3·5; using as indicators,
-peridot or idocrase 3·40 and topaz 3·53.
-
-(_f_) Silver-thallium nitrate, reduced to 4·0; indicators, topaz 3·53
-and sapphire 4·03.
-
-(_g_) Silver-thallium nitrate, undiluted, 4·6.
-
-The tubes must be heated in some form of water-bath; an ordinary glass
-beaker serves the purpose satisfactorily. The pure salt should never be
-diluted; but the density of the contents of tubes (_e_) and (_f_) may
-be varied at will, water being added in order to lower the density, and
-concentration by means of evaporation or addition of the nitrate being
-employed in order to increase it. To avoid the discoloration of the
-skin, rubber finger-stalls may be used, and the stones should not be
-handled until after they have been washed in warm water. The staining
-may be minimized if the hands be well washed in hot water before being
-exposed to sunlight. It is advisable to warm the stone to be tested
-in a tube containing water beforehand lest the sudden heating develop
-cracks. A piece of platinum, or, failing that, copper wire is of
-service for removing stones from the tubes; a glass rod, spoon-shaped
-at one end, does equally well. It must be noted that although Retgers’s
-salt is absolutely harmless to the ordinary gem-stones—with the
-exception of opal and turquoise, which, as has already been stated,
-being to some extent porous, should not be immersed in liquids—it
-attacks certain substances, for instance, sulphides and cannot be
-applied indiscriminately to minerals.
-
-The procedure described above is intended only as a suggestion;
-the method may be varied to any extent at will, depending upon the
-particular requirements. If such tests are made only occasionally, a
-smaller number of tubes may be used. Thus one tube may be substituted
-for the two marked _a_ and _b_, the liquid contained in it being
-diluted as required, and a series of indicators may be kept apart in
-small glass tubes. On the other hand, any one having constantly to test
-stones might increase the number of tubes with advantage, and might
-find it useful to have at hand fragments of all the principal species
-in order to make direct comparison.
-
-
- (2) DIRECT WEIGHING
-
-The balance which is necessary in both the methods described under this
-head should be capable of giving results accurate to milligrams, _i.e._
-the thousandth part of a gram, and consistent with that restriction
-the beam may be as short as possible so as to give rapid swings and
-thus shorten the time taken in the observations. A good assay balance
-answers the purpose admirably. Of course, it is never necessary to wait
-till the balance has come to rest. The mean of the extreme readings of
-the pointer attached to the beam will give the position in which it
-would ultimately come to rest. Thus, if the pointer just touches the
-eighth division on the right-hand side and the second on the other,
-the mean position is the third division on the right-hand side (½(8 −
-2) = 3). Instead of the ordinary form of chemical balance, Westphal’s
-form or Joly’s spring-balance may be employed. Weighings are made more
-quickly, but are not so accurate.
-
-In refined physical work the practice known as double-weighing is
-employed to obviate any slight error there may be in the suspension
-of the balance. A counterpoise which is heavier than anything to be
-weighed is placed in one pan, and weighed. The counterpoise is retained
-in its pan throughout the whole course of the weighings. Any substance
-whose weight is to be found is placed in the other pan, and weights
-added till the balance swings truly again. The difference between
-the two sets of weights evidently gives the weight of the substance.
-Balances, however, are so accurately constructed that for testing
-purposes such refined precautions are not really necessary.
-
-It is immaterial in what notation the weighings are made, so long as
-the same is used throughout, but the metric system of weights, which
-is in universal use in scientific work, should preferably be employed.
-Jewellers, however, use carat weights, and a subdivision to the base
-2 instead of decimals, the fractions being ½, ¼, ⅛, 1/16, 1/32, 1/64.
-If these weights be employed, it will be necessary to convert these
-fractions into decimals, and write ½ = ·500, ¼ ·250, ⅛ = ·125, 1/16 =
-·062, 1/32 = ·031, 1/64 = ·016.
-
-
- (a) _Hydrostatic Weighing_
-
-The principle of this method is very simple. The stone, the specific
-gravity of which is required, is first weighed in air and then when
-immersed in water. If _W_ and _W´_ be these weights respectively, then
-_W_ − _W´_ is evidently the weight of the water displaced by the stone
-and having therefore the same volume as it, and the specific gravity is
- _W_
-therefore equal to ———————————.
- _W_ − _W^r_
-
-If the method of double-weighing had been adopted, the formula would
-be slightly altered. Thus, suppose that _c_ corresponds to the
-counterpoise, _w_ and _w´_ to the stone weighed in air and water
-respectively; then we have _W_ = _c_ − _w_ and _W´_ = _c_ − _w´_, and
- _c_ − _w_
-therefore the specific gravity is equal to ——————————.
- _w´_ − _w_
-
-[Illustration: FIG. 33.—Hydrostatic Balance.]
-
-Some precautions are necessary in practice to assure an accurate
-result. A balance intended for specific gravity work is provided with
-an auxiliary pan (Fig. 33), which hangs high enough up to permit of
-the stone being suspended underneath. The weight of anything used for
-the suspension must, of course, be determined and subtracted from the
-weight found for the stone, both when in air and when in water. A piece
-of fine silk is generally used for suspending the stone in water,
-but it should be avoided, because the water tends to creep up it and
-the error thus introduced affects the first place of decimals in the
-case of a one-carat stone, the value being too high. A piece of brass
-wire shaped into a cage is much to be preferred. If the same cage be
-habitually used, its weight in air and when immersed in water to the
-customary extent in such determinations should be found once for all.
-
-Care must also be taken to remove all air-bubbles which cling to the
-stone or the cage; their presence would tend to make the value too low.
-The surface tension of water which makes it cling to the wire prevents
-the balance swinging freely, and renders it difficult to obtain a
-weighing correct to a milligram when the wire dips into water. This
-difficulty may be overcome by substituting a liquid such as toluol,
-which has a much smaller surface tension.
-
-As has been stated above, the density of water at 4° C. is taken as
-unity, and it is therefore necessary to multiply the values obtained
-by the density of the liquid, whatever it be, at the temperature of
-the observation. In Table IX, at the end of the book, are given the
-densities of water and toluol at ordinary room-temperatures. It will be
-noticed that a correct reading of the temperature is far more important
-in the case of toluol.
-
-
- _Example of a Hydrostatic Determination of Specific Gravity—_
-
- Weight of stone in air = 1·471 gram
- Weight of stone in water = 1·067 „
- 1·471 1·471
- Specific gravity = ————————————— = —————
- 1·471 − 1·067 0·404.
-
-Allowing for the density of water at the temperature of the room, which
-was 16° C., the specific gravity is 3·637. Had no such allowance been
-made, the result would have been four units too high in the third place
-of decimals. For discriminative purposes, however, such refinement is
-unnecessary.
-
-
- (b) _Pycnometer, or Specific Gravity Bottle_
-
-The specific gravity bottle is merely one with a fairly long neck on
-which a horizontal mark has been scratched, and which is closed by
-a ground glass stopper. The pycnometer is a refined variety of the
-specific gravity bottle. It has two openings: the larger is intended
-for the insertion of the stone and the water, and is closed by a
-stopper through which a thermometer passes, while the other, which is
-exceedingly narrow, is closed by a stopper fitting on the outside, and
-is graduated to facilitate the determination of the height of the water
-in it.
-
-The stone is weighed as in the previous method. The bottle is then
-weighed, and filled with water up to the mark and weighed again. The
-stone is now introduced into the bottle, and the surplus water removed
-with blotting-paper or otherwise until it is at the same level as
-before, and the bottle with its contents is weighed. Let _W_ be the
-weight of the stone, _w_ the weight of the bottle, _W_´ the weight of
-the bottle and the water contained in it, and _W_″ the weight of the
-bottle when containing the stone and the water. Then _W_´ − _w_ is the
-weight of the water filling the bottle up to the mark, and
-_W_″ − _w_ − _W_ is the reduced weight of water after the stone has
-been inserted; the difference, _W_ + _W_´ − _W_″, is the weight of the
- _W_
-water displaced. The specific gravity is therefore ——————————————————.
- _W_ + _W_´ − _W_″
-As in the previous method, this value must be multiplied by the density
-of the liquid at the temperature of the experiment. If the method of
-double-weighing be adopted, the formula will be slightly modified.
-
- • • • • •
-
-Of the above methods, that of heavy liquids, as it is usually termed,
-is by far the quickest and the most convenient for stones of ordinary
-size, the specific gravity of which is less than the density of pure
-methylene iodide, namely, 3·324, and by its aid a value may be obtained
-which is accurate to the second place of decimals, a result quite
-sufficient for a discriminative test. The method is applicable no
-matter how small the stone may be, and, indeed, for very small stones
-it is the only trustworthy method; for large stones it is inconvenient,
-not only because of the large quantity of liquid required, but also
-on account of the difficulty in estimating with sufficient certainty
-the position of the centre of gravity of the stone. A negative
-determination may be of value, especially if attention be paid to the
-rate at which the stone falls through the liquid; the denser the stone
-the faster it will sink, but the rate depends also upon the shape of
-the stone. Retgers’s salt is less convenient because of the delay
-involved in warming it and of the almost inevitable staining of the
-hands, but its use presents no difficulty whatever.
-
-Hydrostatic weighing is always available, unless the stone be very
-small, but the necessary weighings occupy considerable time, and care
-must be taken that no error creeps into the computation, simple though
-it be. Even if everything is at hand, a determination is scarcely
-possible under a quarter of an hour.
-
-The third method, which takes even longer, is intended primarily for
-powdered substances, and is not recommended for cut stones, unless
-there happen to be a number of tiny ones which are known to be exactly
-of the same kind.
-
-The specific gravities of the gem-stones are given in Table VII at the
-end of the book.
-
-
-
-
- CHAPTER IX
-
- HARDNESS AND CLEAVABILITY
-
-
-Every possessor of a diamond ring is aware that diamond easily
-scratches window-glass. If other stones were tried, it would be
-found that they also scratched glass, but not so readily, and, if
-the experiment were extended, it would be found that topaz scratches
-quartz, but is scratched by corundum, which in its turn yields to
-the all-powerful diamond. There is therefore considerable variation
-in the capacity of precious stones to resist abrasion, or, as it is
-usually termed, in their hardness. To simplify the mode of expressing
-this character the mineralogist Mohs about a century ago devised the
-following arbitrary scale, which is still in general use.
-
-
- MOHS’S SCALE OF HARDNESS
-
- 1. Talc
- 2. Gypsum
- 3. Calcite
- 4. Fluor
- 5. Apatite
- 6. Orthoclase
- 7. Quartz
- 8. Topaz
- 9. Corundum
- 10. Diamond
-
-A finger-nail scratches gypsum and softer substances. Ordinary
-window-glass is slightly softer than orthoclase, and a steel knife is
-slightly harder; a hardened file approaches quartz in hardness, and
-easily scratches glass.
-
-By saying that a stone has hardness 7 we merely mean that it will not
-scratch quartz, and quartz will not scratch it. The numbers indicate
-an order, and have no quantitative significance whatever. This is an
-important point about which mistakes are often made. We must not, for
-instance, suppose that diamond has twice the hardness of apatite.
-As a matter of fact, the interval between diamond and corundum is
-immensely greater than that between the latter and talc, the softest
-of mineral substances. Intermediate degrees of hardness are expressed
-by fractions. The number 8½ for chrysoberyl means that it scratches
-topaz as easily as it itself is scratched by corundum. Pyrope garnet is
-slightly harder than quartz, and its hardness is said therefore to be
-7¼.
-
-Delicate tests show that the structure of all crystallized substances
-is more or less grained, like that of wood, and the hardness for the
-same stone varies in different directions. Kyanite is unique in this
-respect, since its hardness ranges from 5 to 7; it can therefore
-be scratched by a knife in some directions, but not in others. In
-most substances, however, the range is so small as to be quite
-imperceptible. Slight variation is also apparent in the hardness of
-different specimens of the same species. The diamonds from Borneo and
-New South Wales are so distinctly harder than those from South Africa
-and other localities that, when first discovered, some difficulty was
-experienced in cutting them. Again, lapidaries find that while Ceylon
-sapphires are harder than rubies, Kashmir sapphires are softer.
-
-Hardness is a character of fundamental importance in a stone intended
-for ornamental wear, since upon it depends the durability of the polish
-and brilliancy. Ordinary dust is largely composed of grains of sand,
-which is quartz in a minute form, and a gem-stone should therefore
-be at least as hard as that. Paste imitations are little harder than
-5, and consequently, as experience shows, their polish does not
-survive a few weeks’ wear. Hardness is, however, of little use as a
-discriminative test except for distinguishing between topaz or harder
-stone and paste. Diamond is so much harder than other stones that it
-will leave a cut in glass quite different from the scratch of even
-corundum. Paste, being so soft, readily yields to the file, and is thus
-easily distinguished from genuine stones. In applying the test to a
-cut stone, it is best to remove it from its mount and try the effect
-on the girdle, because any scratch would be concealed afterwards by
-the setting. Any mark should be rubbed with the finger to assure that
-it is not due to powder from the scratching agent; confusion may often
-be caused in this way when the two substances are of nearly the same
-hardness.
-
-The degrees of hardness of the gem-stones are given in Table VIII at
-the end of the book.
-
- • • • • •
-
-It must not be overlooked that extreme hardness is compatible with
-cleavability in certain directions intimately connected with the
-crystalline structure; the property, in fact, characterizes many
-mineral species of different degrees of hardness. Diamond can be split
-in four directions parallel to the faces of the regular octahedron,
-a property utilized by the lapidary for shaping a stone previous to
-cutting it. Topaz cleaves with considerable ease at right angles to the
-principal crystallographic axis. Felspar has two directions of cleavage
-nearly at right angles to one another. The new gem-stone, kunzite,
-needs cautious handling owing to the facility with which it splits in
-two directions mutually inclined at about 70°.
-
-All stones are more or less brittle, and will be fractured by a
-sufficiently violent blow, but the irregular surface of a fracture
-cannot be mistaken for the brilliant flat surface given by a cleavage.
-The cleavage is by no means induced with equal facility in the species
-mentioned above. A considerable effort is required to split diamond,
-but in the case of topaz or kunzite incipient cleavage in the shape of
-flaws may be started if the stone be merely dropped on to a hard floor.
-
-
-
-
- CHAPTER X
-
- ELECTRICAL CHARACTERS
-
-
-The definite orientation of the molecular arrangement of crystallized
-substances leads in many cases to attributes which vary with the
-direction and are revealed by the electrical properties. If a
-tourmaline crystal be heated in a gas or alcohol flame it becomes
-charged with electricity, and, since it is at the same time a bad
-conductor, static charges of opposite sign appear at the two ends.
-Topaz shows similar characters, but in a lesser degree. Quartz, if
-treated in the same way, shows charges of opposite sign on different
-sides, but the phenomenon may be masked by intimate twinning and
-consequent overlapping of the contrary areas. The phenomenon may
-also be seen when the stones are cut. The most convenient method for
-detecting the existence of the electrical charges is that devised
-by Kundt. A powder consisting of a mixture of red lead and sulphur
-is placed in a bellows arrangement and blown through a sieve at one
-end on to the stone. Owing to the friction the particles become
-electrified—red lead positively and sulphur negatively—and are
-attracted by the charges of opposing sign, which will therefore be
-betrayed by the colour of the dust at the corresponding spot. The
-powder must be kept dry; otherwise a chemical reaction may occur
-leading to the formation of lead sulphide, recognizable by its black
-colour. Bücker has suggested as an alternative the use of sulphur,
-coloured red with carmine, the negative element, and yellow lycopodium,
-the positive element.
-
-Diamond, topaz, and tourmaline are powerful enough, when electrified
-by friction with a cloth, to attract fragments of paper, the
-electrification being positive. Amber develops considerable negative
-electricity when treated in a similar manner.
-
-Diamond is translucent to the Röntgen (X) rays; glass, on the other
-hand, is opaque to them, and this test distinguishes brilliants from
-paste imitations. Diamond also, unlike glass, phosphoresces under the
-influence of radium, a property characterizing also kunzite.
-
-It will be seen that the electrical characters, although of
-considerable interest to the student, are, on account of their
-limited application and difficulty of test, of little service for the
-discrimination of gem-stones.
-
-
-
-
- PART I—SECTION B
-
- THE TECHNOLOGY OF GEM-STONES
-
-
-
-
- CHAPTER XI
-
- UNIT OF WEIGHT
-
-
-The system in use for recording the weights of precious stones is
-peculiar to jewellery. The unit, which is known as the carat, bears no
-simple relation to any unit that has existed among European nations,
-and indubitably has been introduced from the East. When man in early
-days sought to record the weights of small objects, he made use of the
-most convenient seeds or grains which were easily obtainable and were
-at the same time nearly uniform in size. In Europe the smallest unit of
-weight was the barley grain. Similarly in the East the seeds of some
-leguminous tree were selected. Those of the locust-tree, _Ceratonia
-siliqua_, which is common in the countries bordering the Mediterranean,
-on the average weigh so nearly a carat that they almost certainly
-formed the original unit. It is, indeed, from the Greek κεράτιον,
-little horn, which refers to the shape of the pods, that the word carat
-is derived.
-
-It is one of the eccentricities of the jewellery trade that precision
-should not have been given to the unit of weight. Not only does it
-vary at most of the trade centres in the world, but it is not even
-always constant at each centre. The difference is negligible in the
-case of single stones of ordinary size, but becomes a matter of serious
-importance when large stones, or parcels of small stones, are bought
-and sold, particularly when the stones are very costly. Attempts have
-been made at various times to secure a uniform standard, but as yet
-with only partial success. In 1871 the carat defined as the equivalent
-of 0·20500 gram was suggested at a meeting of the principal jewellers
-of Paris and London, and was eventually accepted in Paris, New York,
-Leipzig, and Borneo. It has, however, recently been recognized that
-in view of the gradual spread of the metric system of weights and
-measures the most satisfactory unit is the metric carat of one-fifth
-(0·2) gram. This has now been constituted the legal carat of France
-and Belgium, and no doubt other countries will follow their example.
-The carat weight obtaining in London weighs about 0·20530 gram, and
-the approximate equivalents in the gram at other centres are as
-follows:—Florence 0·19720, Madrid 0·20539, Berlin 0·20544, Amsterdam
-0·20570, Lisbon 0·20575, Frankfort-on-Main 0·20577, Vienna 0·20613,
-Venice 0·20700, and Madras 0·20735. The gram itself is inconveniently
-large to serve as a unit for the generality of stones met with in
-ordinary jewellery.
-
-The notation for expressing the sub-multiples of the carat forms
-another curious eccentricity. Fractions are used which are powers of
-the half: thus the half, the half of that, _i.e._ the quarter, and so
-on down to the sixty-fourth, and the weight of a stone is expressed
-by a series of fractions, _e.g._ 3½ ⅛ 1/64 carats. In the case of
-diamond a single unreduced fraction to the base 64 is substituted in
-place of the series of single fractions, and the weight of a stone is
-stated thus, 4-40/64 carats. With the introduction of the metric
-carat the more convenient and rational decimal notation would, of
-course, be simultaneously adopted.
-
-[Illustration: Figs. 34-39.—Exact Sizes of Brilliants of various
-Weights.]
-
-Figs. 34-39 illustrate the exact sizes of diamonds of certain weights,
-when cut as brilliants. The sizes of other stones depends upon their
-specific gravity, the weight varying as the volume multiplied by the
-specific gravity. Quartz, for instance, has a low specific gravity and
-would be perceptibly larger, weight for weight; zircon, on the other
-hand, would be smaller.
-
-It has been found more convenient to select a smaller unit in the case
-of pearls, namely, the pearl-grain, four of which go to the carat.
-
-Stencil gauges are in use for measuring approximately the weight in
-carats of diamond brilliants and of pearls, which in both instances
-must be unmounted. A more accurate method for determining the weight
-of diamonds has been devised by Charles Moe, which is applicable to
-either unmounted or mounted stones. By means of callipers, which read
-to three-tenths of a millimetre, the diameter and the depth of the
-stone are measured, and by reference to a table the corresponding
-weight is found; allowance is made for the varying fineness of the
-girdle, and, in the case of large stones, for the variation from a
-strictly circular section.
-
- • • • • •
-
-Since this chapter was written the movement in favour of the metric
-carat has made rapid progress, and this unit will soon have been
-adopted as the legal standard all over the world, even in countries,
-such as the British Isles and the United States, where the metric
-system is not in use. The advantage of an international unit is too
-obvious to need arguing.
-
-
-
-
- CHAPTER XII
-
- FASHIONING OF GEM-STONES
-
-
-Although many of the gem-stones have been endowed by nature with
-brilliant lustrous faces and display scintillating reflections from
-their surfaces, yet their form is never such as to reveal to full
-perfection the optical qualities upon which their charm depends.
-Moreover, the natural faces are seldom perfect; as a rule the stones
-are broken either through some convulsion of the earth’s crust or in
-course of extraction from the matrix in which they have lain, or they
-are roughened by attrition against matter of greater hardness, or worn
-by the prolonged action of water, or etched by solvents. Beautiful
-octahedra of diamond or spinel have been mounted without further
-embellishment, but even their appearance might have been much improved
-at the lapidary’s hands.
-
-By far the oldest of the existing styles of cutting is the rounded
-shape known as cabochon, a French word derived from the Latin _cabo_,
-a head. In the days of the Roman Empire the softer stones were often
-treated in this manner; such stones were supposed to be beneficial
-to those suffering from short-sightedness, the reason no doubt being
-that transparent stones when cut as a double cabochon formed a convex
-lens. According to Pliny, Nero had an emerald thus cut, through
-which he was accustomed to view the gladiatorial shows. This style of
-cutting was long a favourite for coloured stones, such as emerald,
-ruby, sapphire, and garnet, but has been abandoned in modern practice
-except for opaque, semi-opaque, and imperfect stones. The crimson
-garnet, which was at one time known by the name carbuncle, was so
-systematically thus cut that the word has come to signify a red garnet
-of this form. It was a popular brooch-stone with our grandmothers, but
-is no longer in vogue. The East still retains a taste for stones cut
-in the form of beads and drilled through the centre; the beads are
-threaded together, and worn as necklaces. The native lapidaries often
-improve the colour of pale emeralds by lining the hole with green paint.
-
-[Illustration: _PLATE V_
-
-JEWELLERY DESIGNS]
-
-[Illustration: FIG. 40.—Double (Convex) Cabochon.]
-
-[Illustration: FIG. 41.—Simple Cabochon.]
-
-The cabochon form may be of three different kinds. In the first, the
-double cabochon (Fig. 40), both the upper and the under sides of the
-stones are curved. The curvature, however, need not be the same in
-each case; indeed, it is usually markedly different. Moonstones and
-starstones are generally cut very steep above and shallow underneath.
-Occasionally a ruby or a sapphire is, when cut in this way, set with
-the shallow side above, because the light that has penetrated into the
-stone from above is more wholly reflected from a steep surface with
-consequent increase in the glow of colour from the stone. Opals are
-always cut higher on the exposed side, but the slope of the surface
-varies considerably; they are generally cut steeply when required for
-mounting in rings. Chrysoberyl cat’s-eyes are invariably cut with
-curved bases in order to preserve the weight as great as possible.
-The double cabochon form with a shallow surface underneath merges
-into the second kind (Fig. 41) in which the under side is plane, the
-form commonly employed for quartz cat’s-eyes, and occasionally also
-for carbuncles. In this type the plane side is invariably mounted
-downwards. In the third form (Fig. 42) the curvature of the under
-surface is reversed, and the stone is hollowed out into a concave
-shape. This style is reserved for dark stones, such as carbuncles,
-which, if cut at all thick, would show very little colour. A piece of
-foil is often placed in the hollow in order to increase the reflection
-of light, and thus to heighten the colour effect.
-
-[Illustration: FIG. 42.—Double (Concavo-convex) Cabochon.]
-
-In early days it was supposed that the extreme hardness of diamond
-precluded the possibility of fashioning it, and up to the fifteenth
-century all that was done was to remove the gum-like skin which
-disfigured the Indian stones and to polish the natural facets.
-The first notable advance was made in 1475, when Louis de Berquem
-discovered, as it is said quite by accident, that two diamonds if
-rubbed together ground each other. With confident courage he essayed
-the new art upon three large stones entrusted to him by Charles the
-Bold, to the entire satisfaction of his patron. The use of wheels
-or discs charged with diamond dust soon followed, but at first the
-lapidaries evinced their victory over such stubborn material by
-grinding diamond into divers fantastic shapes, and failed to realize
-how much might be done to enhance the intrinsic beauty of the stones by
-the means now at their disposal. The Indian lapidaries arrived at the
-same discovery independently, and Tavernier found, when visiting the
-country in 1665, a large number of diamond cutters actively employed.
-If the stone were perfectly clear, they contented themselves with
-polishing the natural facets; but if it contained flaws or specks, they
-covered it with numerous small facets haphazardly placed. The stone was
-invariably left in almost its original shape, and no effort was made to
-improve the symmetry.
-
-[Illustration: FIG. 43.—Table Cut (top view).]
-
-[Illustration: FIG. 44.—Table Cut (side view).]
-
-For a long time little further progress was made, and even nearly a
-century after Berquem the only regular patterns known to Kentmann, who
-wrote in 1562, were the diamond-point and the diamond-table (Figs.
-43-44). The former consisted of the natural octahedron facets ground
-to regular shape, and was long employed for the minute stones which
-were set in conjunction with large coloured stones in rings. The table
-represented considerably greater labour. One corner of the regular
-octahedron was ground down until the artificial facet thus produced was
-half the width of the stone, while the opposite corner was slightly
-ground.
-
-Still another century elapsed before the introduction of the rose
-pattern, which comprised twenty-four triangular facets and a flat base
-(Figs. 45-46), the stone being nearly hemispherical in shape. This
-style is said to have been the invention of Cardinal Mazarin, but
-probably he was the first to have diamonds of any considerable size cut
-in this form. At the present day only tiny stones are cut as roses.
-
-[Illustration: FIG. 45.—Rose Cut (top view).]
-
-A few more years passed away, and at length at the close of the
-seventeenth century diamond came by its own when Vincenzio Peruzzi, a
-Venetian, introduced the brilliant form of cutting, and revealed for
-the first time its amazing ‘fire.’ Except for minor changes this form
-remains to this day the standard style for the shape of diamond, and
-the word brilliant is commonly employed to denote diamond cut in this
-way. So obviously and markedly superior is the style to all others
-that upon its discovery the owners of large roses had them re-cut as
-brilliants despite the loss in weight necessitated by the change.
-
-[Illustration: FIG. 46.—Rose Cut (side view).]
-
-The brilliant form is derived from the old table by increasing the
-number of facets and slightly altering the angles pertaining to the
-natural octahedron. In a perfect brilliant (Figs. 47-49) there are
-altogether 58 facets, 33 above and 25 below the girdle, as the edge
-separating the upper and lower portions of the stone is termed, which
-are arranged in the following manner. Eight star-facets, triangular
-in shape, immediately surround the large table-facet. Next come four
-large templets or bezels, quadrilateral in form, arranged in pairs
-on opposite sides of the table-facet, the four quoins or lozenges,
-similar in shape, coming intermediately between them; in modern
-practice, however, these two sets are identical in shape and size,
-and there are consequently eight facets of the same kind instead of
-two sets of four. The eight cross or skew facets and the eight skill
-facets, in both sets the shape being triangular, form the boundary
-of the girdle; modern brilliants usually have instead sixteen facets
-of the same shape and size. The above 33 facets lie above the girdle
-and form the crown of the stone. Immediately opposite and parallel to
-the table is the tiny culet. Next to the latter come the four large
-pavilion facets with the four quoins intermediately between them,
-both sets being five-sided but nearly quadrilateral in shape; these
-again are usually combined into eight facets of the same size. Eight
-cross facets and eight skill facets, both sets, like those in the
-crown, being triangular in shape, form the lower side of the girdle;
-these also are generally united into a set of sixteen similar facets.
-These 25 facets which lie below the girdle comprise the ‘pavilion,’
-or base of the stone. In a regular stone properly cut a templet is
-nearly parallel to a pavilion, and an upper to a lower cross facet. The
-contour of the girdle is usually circular, but occasionally assumes
-less symmetrical shapes, as for instance in drop-stones or pendeloques,
-and the facets are at the same time distorted. The number of facets may
-with advantage be increased in the case of large stones. An additional
-set of eight star facets is often placed round the culet, the total
-number then being 66. It may be mentioned that the largest stone cut
-from the Cullinan has the exceptional number of 74 facets.
-
-[Illustration: FIG. 47.—Brilliant Cut (top view).]
-
-[Illustration: FIG. 48.—Brilliant Cut (base view).]
-
-[Illustration: FIG. 49.—Brilliant Cut (side view).]
-
-In order to secure the finest optical effect certain proportions have
-been found necessary. The depth of the crown must be one-half that of
-the base, and therefore one-third the total depth of the stone, and the
-width of the table must be slightly less than half that of the stone.
-The culet should be quite small, not more in width than one-sixth of
-the table; it is, in fact, not required at all except to avoid the
-danger of the point splintering. The girdle should be as thin as is
-compatible with strength sufficient to prevent chipping in the process
-of mounting the stone; if it were left thick, the rough edge would be
-visible by reflection at the lower facets, and would, especially if at
-all dirty, seriously affect the quality of the stone. The shape of the
-stone is largely determined by the sizes of the templets in the crown
-and the pavilions in the base as compared with that of the table, or,
-what comes to the same thing, by the inclinations at which they are cut
-to that facet. If the table had actually half the width of the stone,
-the angle[5] between it and a templet would be exactly half a right
-angle or 45°; it is, however, made somewhat smaller, namely, about 40°.
-A pavilion, being parallel to a templet, makes a similar angle with the
-culet. The cross facets are more steeply inclined, and make an angle
-of about 45° with the table or the culet, as the case may be. The star
-facets, on the other hand, slant perceptibly less, and make an angle of
-only about 26° with the table. A latitude of some 4° or 5° is possible
-without seriously affecting the ‘fire’ of the stone.
-
-The object of the disposition of the facets on a brilliant is to assure
-that all the light that enters the stone, principally by way of the
-table, is wholly reflected from the base and emerges through the crown,
-preferably by way of the inclined facets. A brilliant-cut diamond, if
-viewed with the table between the observer and the light, appears quite
-dark except for the small amount of light escaping through the culet.
-Light should therefore fall on the lower facets at angles greater
-than the critical angle of total-reflection, which for diamond is 24°
-26´. The pavilions should be inclined properly at double this angle,
-or 48° 52´, to the culet; but a ray that emerges at a pavilion in the
-actual arrangement entered the table at nearly grazing incidence, and
-the amount of light entering this facet at such acute perspective is
-negligible. On the other hand, after reflection at the base light must,
-in order to emerge, fall on the crown at less than the critical angle
-of total-reflection. In Fig. 50 are shown diagrammatically the paths
-of rays that entered the table in divers ways. The ray emerging again
-at the table suffers little or no dispersion and is almost white,
-but those coming out through the inclined facets are split up into
-the rainbow effect, known as ‘fire,’ for which diamond is so famous.
-It is in order that so much of the light entering by the table may
-emerge through the inclined facets of the crown that the pavilions are
-inclined at not much more than 40° to the culet. It might be suggested
-that instead of being faceted the stone should be conically shaped,
-truncated above and nearly complete below. The result would no doubt
-be steadier, but, on the other hand, far less pleasing. It is the
-ever-changing nuance that chiefly attracts the eye; now a brilliant
-flash of purest white, anon a gleam of cerulean blue, waxing to
-richest orange and dying in a crimson glow, all intermingled with the
-manifold glitter from the surface of the stone. Absolute cleanliness is
-essential if the full beauty of any stone is to be realized, but this
-is particularly true of diamond. If the back of the stone be clogged
-with grease and dirt, as so often happens in claw-set rings, light is
-no longer wholly reflected from the base; much of it escapes, and the
-amount of ‘fire’ is seriously diminished.
-
-[Illustration: FIG. 50.—Course of the Rays of Light passing through a
-Brilliant.]
-
-Needless to state, lapidaries make no careful angular measurements
-when cutting stones, but judge of the position of the facets entirely
-by eye. It sometimes therefore happens that the permissible limits
-are overstepped, in which event the stone is dead and may resist all
-efforts to vivify it short of the heroic course of re-cutting it, too
-expensive a treatment in the case of small stones.
-
-The factors that govern the properties of a brilliant-cut stone are
-large colour-dispersion, high refraction, and freedom from any trace of
-intrinsic colour. The only gem-stone that can vie with diamond in these
-respects is zircon. Although it is rare to find a zircon naturally
-without colour, yet many kinds are easily deprived of their tint by
-the application of heat. A brilliant-cut zircon is, indeed, far from
-readily distinguished by eye from diamond, and has probably often
-passed as one, but it may easily be identified by its large double
-refraction (cf. p. 41) and inferior hardness. The remaining colourless
-stones, such as white sapphire, topaz, and quartz (rock-crystal), have
-insufficient refractivity to give total-reflection at the base, and,
-moreover, they are comparatively deficient in ‘fire.’
-
-[Illustration: FIG. 51.—Step- or Trap-Cut (top view).]
-
-[Illustration: FIG. 52.—Step- or Trap-Cut (side view).]
-
-A popular style of cutting which is much in vogue for coloured stones
-is the step- or trap-cut, consisting of a table and a series of
-facets with parallel horizontal edges (Figs. 51-52) above and below
-the girdle; in recent jewellery, however, the top of the stone is
-often brilliant-cut. The contour may be oblong, square, lozenge, or
-heart-shaped, or have less regular forms. The table is sometimes
-slightly rounded. Since the object of this style is primarily to
-display the intrinsic colour of the stone and not so much a brilliant
-play of light from the interior, no attempt is made to secure
-total-reflection at the lower facets. The stone therefore varies in
-depth according to its tint; if dark, it is cut shallow, lest light
-be wholly absorbed within, and the stone appear practically opaque,
-but if light, it is cut deep, in order to secure fullness of tint.
-Much precision in shape and disposition of the facets is not demanded,
-and the stones are usually cut in such a way that, provided the
-desired effect is obtained, the weight is kept as great as possible;
-we may recall that stones are sold by weight. In considering what
-will be the optical effect of any particular shape, regard must be
-had to the effective colour of the transmitted light. For instance,
-although sapphire and ruby belong to the same species and have the
-same refractive indices, yet, since the former transmits mainly blue
-and the latter red light, they have for practical purposes appreciably
-different indices, and lapidaries find it therefore possible to cut
-the base of ruby thicker than that of sapphire, and thus keep the
-weight greater. It is instructive too what can be done with the most
-unpromising material by the exercise of a little ingenuity. Thus Ceylon
-sapphires are often so irregularly coloured that considerable skill
-is called for in cutting them. A stone may, for instance, be almost
-colourless except for a single spot of blue; yet, if the stone be
-cut steeply and the spot be brought to the base, the effect will be
-precisely the same as if the stone were uniformly coloured, because all
-the light emerging from the stone has passed through the spot at the
-base and therefore been tinted blue.
-
-The mechanism employed in the fashioning of gem-stones is simple in
-character, and comprises merely metal plates or wheels for slitting,
-and discs or laps for grinding and polishing the stones, the former
-being set vertically and rotated about horizontal spindles, and the
-latter set horizontally and rotated about vertical spindles. Mechanical
-power is occasionally used for driving both kinds of apparatus, but
-generally, especially in slitting and in delicate work, hand-power is
-preferred. In the East native lapidaries make use of vertical wheels
-(Plate XIII) also for grinding and polishing stones, which explains why
-native-cut stones never have truly plane facets; it will be noticed
-from the picture that a long bow is used to drive the spindle.
-
-Owing to the unique hardness of diamond it can be fashioned only by
-the aid of its own powder. The process differs therefore materially
-from the cutting of the remaining gem-stones, and will be described
-separately. Indeed, so different are the two classes of work that firms
-seldom habitually undertake both.
-
-The discovery of the excellent cleavage of diamond enormously reduced
-the labour of cutting large stones. A stone containing a bad flaw may
-be split to convenient shape in as many minutes as the days or even
-weeks required to grind it down. The improvement in the appliances and
-the provision of ample mechanical power has further accelerated the
-process and reduced the cost. Two years were occupied in cutting the
-diamond known as the Pitt or Regent, whereas in only six months the
-colossal Cullinan was shaped into two large and over a hundred smaller
-stones with far less loss of material.
-
-Although the brilliant form was derived from the regular octahedron, it
-by no means follows that, because diamond can be cleaved to the latter
-form, such is the initial step in fashioning the rough mass. The aim of
-the lapidary is to cut the largest possible stone from the given piece
-of rough, and the finished brilliant usually bears no relation whatever
-to the natural octahedron. The cleavage is utilized only to free the
-rough of an awkward and useless excrescence, or of flaws. Although the
-octahedron is one of the common forms in which diamond is found, it is
-rarely regular, and oftener than not one of the larger faces is made
-the table.
-
-The old method, which is still in use, for roughly fashioning diamonds
-is that known as bruting, from the French word, _brutage_, for the
-process, or as shaping. Two stones of about the same size are selected,
-and are firmly attached by means of a hard cement to the ends of
-two holders, which are held one in each hand, and rubbed hard, one
-against the other, until surfaces of the requisite size are developed
-on each stone. During the process the stones are held over a small
-box, which catches the precious powder. A fine sieve at the bottom
-of the box allows the powder to fall through into a tray underneath,
-but holds back anything larger. By means of two vertical pins placed
-one on each side of the box the holders are retained more easily in
-the desired position, and the work is thrown mainly on the thumbs.
-This work continued day after day has a very disfiguring effect upon
-the hands despite the thick gloves that are worn to protect them; the
-skin of the thumbs grows hard and horny, and the first and second
-fingers become swollen and distorted. When the surfaces have thus been
-formed, the stone is handed to the polisher, who works them into the
-correct shape and afterwards polishes them, the stone passing backwards
-and forwards several times between the cutter and the polisher. The
-table, four templets, culet and four pavilions are first formed and
-polished, so that the table has a square shape. Next the quoins are
-developed and polished, and finally the small facets are polished on,
-not being shaped first. In modern practice the process of bruting has
-been modified in some cases by the introduction of machinery, and the
-facets are ground on, with considerable improvement in the regularity
-of their size and disposition, and reduction in the amount of polishing
-required. Moreover, to obviate the loss of material resulting from
-continued grinding, large stones are first sliced by means of
-rapidly-revolving copper wheels charged with diamond powder.
-
-The laps used for polishing diamonds are made of a particular kind
-of soft iron, which is found to surpass any other metal in retaining
-the diamond powder. They are rotated at a high rate of speed, which
-is about 2000 to 2500 revolutions a minute, and the heat developed by
-the friction at this speed is too great for a cement to be used; a
-solder or fusible alloy, composed of one part tin to three parts lead,
-therefore takes its place. The solder is held in a hollow cup of brass
-which is from its shape called a ‘dop,’ an old Dutch word meaning
-shell. Its external diameter is ordinarily about 1½ in. (4 cm.), but
-larger dops are, of course, used for large stones. A stout copper stalk
-is attached to the bottom of the dop; it is visible in the view of the
-dop shown at _e_ on Plate VI, and two slabs of solder are seen lying in
-front of the dop. The dop containing the solder is placed in the midst
-of a non-luminous flame and heated until the solder softens, when it is
-removed by means of the small tongs, _c_, and placed upright on a stand
-such as that shown at _a_. The long tongs, _d_, are used for shaping
-the solder into a cone at the apex of which the diamond is placed. The
-solder is worked well over the stone so that only the part to undergo
-polishing is exposed. A diamond in position is shown at _f_. The top of
-the stand is saucer-shaped to catch the stone should it accidentally
-fall off the dop, and to prevent pieces of solder falling on the hand.
-While still hot, the dop with the diamond in position on the solder is
-plunged into cold water in order to cool it. The fact that the stone
-withstands this drastic treatment is eloquent testimony to its good
-thermal conductivity; other gem-stones would promptly split into
-fragments. It may be remarked that so high is the temperature at which
-diamond burns that it may be placed in the gas flame without any fear
-of untoward results. The dop is now ready for attachment to an arm
-such as that shown at _b_; the stalk of the dop is placed in a groove
-running across the split end of the arm, and is gripped tight by means
-of a screw worked by the nut which is visible in the picture.
-
-[Illustration: _PLATE VI_
-
-APPLIANCES USED FOR POLISHING DIAMONDS.]
-
-[Illustration: _PLATE VII_
-
-POLISHING DIAMONDS]
-
-Four such arms, each with a dop, are used with the polishing lap (Plate
-VII), and each stands on two square legs on the bench. Pins, _p_, in
-pairs are fixed to the bench to prevent the arms being carried round by
-the friction; one near the lap holds the arm not far from the dop, and
-the other engages in a strong metal tongue, which is best seen at the
-end of the arm _b_ on Plate VI. Though the arm, which is made of iron,
-is heavy, yet for polishing purposes it is insufficient, and additional
-lead weights are laid on the top of it, as in the case of the arm
-at the back on Plate VII. The copper stalk is strong, yet flexible,
-and can be bent to suit the position of the facet to be polished; on
-Plate VII the dops _a_ and _b_ are upright, but the other two are
-inclined. In addition to the powder resulting from bruting, boart,
-_i.e._ diamonds useless for cutting, are crushed up to supply polishing
-material, and a little olive oil is used as a lubricant. Owing to the
-friction so much heat is developed that even the solder would soften
-after a time, and therefore, as a precaution, the dop is from time
-to time cooled by immersion in water. The stone has constantly to be
-re-set, about six being the maximum even of the tiny facets near the
-girdle that can be dealt with by varying the inclination of the dop.
-As the work approaches completion the stone is frequently inspected,
-lest the polishing be carried too far for the development of the proper
-amount of ‘fire.’ When finished, the stones are boiled in sulphuric
-acid to remove all traces of oil and dirt.
-
-The whole operation is evidently rough and ready in the extreme; but
-such amazing skill do the lapidaries acquire, that even the most
-careful inspection by eye alone would scarce detect any want of proper
-symmetry in a well-cut stone.
-
-The fashioning of coloured stones, as all the gem-stones apart from
-diamond are termed in the jewellery trade, is on account of their
-inferior hardness a far less tedious operation. They are easily
-slit, for which purpose a vertical wheel (Plate VIII) made of soft
-iron is used; it is charged with diamond dust and lubricated with
-oil, generally paraffin. When slit to the desired size, the stone is
-attached to a conveniently shaped holder by means of a cement, the
-consistency of which varies with the hardness of the stone. It is
-set in the cement in such a way that the plane desired for the table
-facet is at right angles to the length of the holder, and the whole of
-the upper part or crown is finished before the stone is removed from
-the cement. The lower half or base is treated in a similar manner.
-Thus in the process of grinding and polishing the stone is only once
-re-set; as was stated above, diamond demands very different treatment.
-Again, all coloured stones are ground down without any intermediate
-operation corresponding to bruting. The holder is merely held in the
-hand, but to maintain its position more exactly its other end,
-which is pointed, is inserted in one of the holes that are pierced at
-intervals in a vertical spindle placed at a convenient distance from
-the lap (Plate VIII), which one depending upon the inclination of the
-facet to be formed. For hard stones, such as ruby and sapphire, diamond
-powder is generally used as the abrasive agent, while for the softer
-stones emery, the impure corundum, is selected; in recent years the
-artificially prepared carborundum, silicide of carbon corresponding to
-the formula CSi, which is harder than corundum, has come into vogue
-for grinding purposes, but it is unfortunately useless for slitting,
-because it refuses to cling to the wheel. To efface the scratches left
-by the abrasive agent and to impart a brilliant polish to the facets,
-material of less hardness, such as putty-powder, pumice, or rouge, is
-employed; in all cases the lubricant is water. The grinding laps are
-made of copper, gun-metal, or lead; and pewter or wooden laps, the
-latter sometimes faced with cloth or leather, are used for polishing.
-As a general rule, the harder the stone the greater the speed of the
-lap.
-
-[Illustration: _PLATE VIII_
-
-SLITTING COLOURED STONES
-
-POLISHING COLOURED STONES]
-
-[Illustration: _PLATE IX_
-
-FACETING MACHINE]
-
-As in the case of diamond, the lapidary judges of the position of the
-facet entirely by eye and touch, but a skilled workman can develop
-a facet very close to the theoretical position. During recent years
-various devices have been invented to enable him to do his work with
-greater facility. A machine of this kind is illustrated on Plate IX.
-The stone is attached by means of cement to the blunt end, _d_, of
-the holder, _b_, which is of the customary kind, while the other end
-is inserted in a hole in a wooden piece, _a_, which is adjustable in
-height by means of the screw above it. The azimuthal positions of the
-facets are arranged by means of the octagonal collar, _c_, the sides
-of which are held successively in turn against the guide, _e_. The
-stand itself is clamped to the bench. The machine is, however, little
-used except for cheap stones, because it is too accurate and leads to
-waste of material. Stones are sold by weight, and so long as the eye is
-satisfied, no attempt is made to attain to absolute symmetry of shape.
-
-The pictures on Plates X-XIII illustrate lapidaries’ workshops in
-various parts of the world. The first two show an office and a workshop
-situated in Hatton Garden, London; in the former certain of the staff
-are selecting from the parcels stones suitable for cutting. The third
-depicts a more primitive establishment at Ekaterinburg in the Urals.
-The fourth shows a typical French family—_père_, _mère_, _et fils_—in
-the Jura district, all busily engaged; on the table will be noticed a
-faceting machine of the kind described above. In the fifth picture a
-native lapidary in Calcutta is seen at work with the driving bow in his
-right, and the stone in his left, hand.
-
-A curious difference exists in the systems of charging for cutting
-diamonds and coloured stones. The cost of cutting the latter is
-reckoned by the weight of the finished stone, the rate varying from
-1s. to 8s. a carat according to the character of the stone and the
-difficulty of the work; while in the case of diamonds, on the other
-hand, the weight of the rough material determines the cost, the rate
-being about 10s. to 40s. a carat according to the size, which on the
-average is equivalent to about 30s. to 120s. a carat calculated on
-the weight of the finished stone. The reason of the distinction is
-obviously because the proper proportions in a brilliant-cut diamond
-must be maintained, whatever be the loss in weight involved; in
-coloured stones the shape is not of such primary importance.
-
-[Illustration: _PLATE X_
-
-LAPIDARY’S WORKSHOP AND OFFICE IN ENGLAND]
-
-[Illustration: _PLATE XI_
-
-LAPIDARY’S WORKSHOP IN RUSSIA]
-
-When finished, the stone finds its way with others akin to it to the
-manufacturing jeweller’s establishment, where it is handed to the
-setter, who mounts it in a ring, necklace, brooch, or whatever article
-of jewellery it is intended for. The metal used in the groundwork of
-the setting is generally gold, but platinum is also employed where an
-unobtrusive and untarnishable metal is demanded, and silver finds a
-place in cheaper jewellery, although it is seriously handicapped by
-its susceptibility to the blackening influence of the sulphurous fumes
-present in the smoke-laden atmosphere of towns. The stone may be either
-embedded in the metal or held by claws. The former is by far the safer,
-but the latter the more elegant, and it has the advantage of exposing
-the stone _à jour_, to use the French jewellers’ expression, so that
-its genuineness is more evidently testified. It is very important
-that the claw setting be periodically examined, lest the owner one
-day experience the mortification of finding that a valuable stone has
-dropped out; gold, owing to its softness, wears away in course of time.
-
-Up to quite recent years modern jewellery was justly open to the
-criticism that it was lacking in variety, that little attempt was made
-to secure harmonious association in either the colour or the lustre of
-the gem-stones, and that the glitter of the gold mount was frequently
-far too obtrusive. Gold consorts admirably with the rich glow of
-ruby, but is quite unsuited to the gleaming fire of a brilliant. Where
-the metal is present merely for the mechanical purpose of holding the
-stones in position, it should be made as little noticeable as possible.
-The artistic treatment of jewellery is, however, receiving now adequate
-attention in the best Paris and London houses. Some recent designs are
-illustrated on Plates IV and V.
-
-[Illustration: _PLATE XII_
-
-FRENCH FAMILY CUTTING STONES]
-
-[Illustration: _PLATE XIII_
-
-INDIAN LAPIDARY]
-
-
-
-
- CHAPTER XIII
-
- NOMENCLATURE OF PRECIOUS STONES
-
-
-The names in popular use for the principal gem-stones may be traced
-back to very early times, and, since they were applied long before
-the determinative study of minerals had become a science, their
-significance has varied at different dates, and is even now far from
-precise. No ambiguity or confusion could arise if jewellers made use
-of the scientific names for the species, but most of them are unknown
-or at least unfamiliar to those unversed in mineralogy, and to banish
-old-established names is undesirable, even if the task were not
-hopeless. The name selected for a gem-stone may have a very important
-bearing on its fortunes. When the love-sick Juliet queried ‘What’s
-in a name?’ her mind was wandering far from jewels; for them a name
-is everything. The beautiful red stones that accompany the diamond
-in South Africa were almost a drug in the market under their proper
-title—garnet, but command a ready sale under the misnomer ‘Cape-ruby.’
-To many minds there is a subtle satisfaction in the possession of a
-stone which is assumed to be a sort of ruby that would be destroyed by
-the knowledge that the stone really belonged to the cinderella species
-of gem-stones—the despised garnet. For similar reasons it was deemed
-advisable to offer the lustrous green garnet found some thirty and odd
-years ago in the Ural Mountains as ‘olivine,’ not a happy choice since
-their colour is grass- rather than olive-green, apart from the fact
-that the term is in general use in science for the species known in
-jewellery as peridot.
-
-The names employed in jewellery are largely based upon the colour, the
-least reliable from a determinative point of view of all the physical
-characters of gem-stones. Qualifying terms are employed to distinguish
-stones of obviously different hardness. ‘Oriental’ distinguishes
-varieties of corundum, but does not imply that they necessarily came
-from the East; the finest gem-stones originally reached Europe by that
-road, and the hardest coloured stones consequently received that term
-of distinction.
-
-Nearly all red stones are grouped under the name ruby, which is derived
-from a Latin word, _ruber_, meaning red, or under other names adapted
-from it, such as rubellite, rubicelle. It is properly applied to red
-corundum; ‘balas’ ruby is spinel, which is associated with the true
-ruby at the Burma mines and is similar in appearance to it when cut,
-and ‘Cape’ ruby, is, as has been stated above, a garnet from South
-Africa. Rubellite is the lovely rose-pink tourmaline, fine examples of
-which have recently been discovered in California, and rubicelle is a
-less pronouncedly red spinel. Sapphire is by far the oldest and one
-of the most interesting of the words used in the language of jewels.
-It occurs in Hebrew and Persian, ancient tongues, and means blue.
-It was apparently employed for lapis lazuli or similar substance,
-but was transferred to the blue corundum upon the discovery of this
-splendid stone. Oblivious of the real meaning of the word, jewellers
-apply it in a quasi-generic sense to all the varieties of corundum
-with the exception of the red ruby, and give vent to such incongruous
-expressions as ‘white sapphire,’ ‘yellow sapphire’; it is true such
-stones often contain traces of blue colour, but that is not the reason
-of the terms. ‘Brazilian’ sapphire is blue tourmaline, a somewhat rare
-tint for this species. The curious history of the word topaz will be
-found below in the chapter dealing with the species of that name. It
-has always denoted a yellow stone, and at the present day is applied
-by jewellers indiscriminately to the true topaz and citrine, the
-yellow quartz, the former, however, being sometimes distinguished by
-the prefix ‘Brazilian.’ ‘Oriental’ topaz is corundum, and ‘occidental’
-topaz is a term occasionally employed for the yellow quartz. Emerald,
-which means green, was first used for chrysocolla, an opaque greenish
-stone (p. 288), but was afterwards applied to the priceless green
-variety of beryl, for which it is still retained. ‘Oriental’ emerald
-is corundum, ‘Brazilian’ emerald in the eighteenth century was a
-common term for the green tourmaline recently introduced to Europe,
-and ‘Uralian’ emerald has been tentatively suggested for the green
-garnet more usually known as ‘olivine.’ Amethyst is properly the violet
-quartz, but with the prefix ‘oriental’ it is also applied to violet
-corundum, though some jewellers use it for the brilliant quartz, with
-purple and white sectors, from Siberia. Almandine, which is derived
-from the name of an Eastern mart for precious stones, has come to
-signify a stone of columbine-red hue, principally garnet, but with
-suitable qualification corundum and spinel also.
-
-The nomenclature of jewellery tends to suggest relations between the
-gem-stones for which there is no real foundation, and to obscure
-the essential identity, except from the point of view of colour, of
-sapphire and ruby, emerald and aquamarine, cairngorm and amethyst.
-
-
-
-
- CHAPTER XIV
-
- MANUFACTURED STONES
-
-
-The initial step in the examination of a crystallized substance is
-to determine its physical characters and to resolve it by chemical
-analysis into its component elements; the final, and by far the
-hardest, step is to build it up or synthetically prepare it from its
-constituents. Unknown to the world at large, work of the latter kind
-has long been going on within the walls of laboratories, and as the
-advance in knowledge placed in the hands of experimenters weapons more
-and more comparable with those wielded by nature, their efforts have
-been increasingly successful. So stupendous, however, are the powers
-of nature that the possibility of reproducing, by human agency, the
-treasured stones which are extracted from the earth in various parts
-of the globe at the cost of infinite toil and labour has always been
-derided by those ignorant of what had already been accomplished. Great,
-therefore, was the consternation and the turmoil when concrete evidence
-that could not be gainsaid showed that man’s restless efforts to
-bridle nature to his will were not in vain, and congresses of all the
-high-priests of jewellery were hastily convened to ban such unrighteous
-products, with what ultimate success remains to be seen.
-
-Crystallization may be caused in four different ways, of which the
-second alone has as yet yielded stones large enough to be cut—
-
-1. By the separation of the substance from a saturated solution. In
-nature the solvent may not be merely hot water, or water charged with
-an acid, but molten rock, and the temperature and the pressure may be
-excessively high.
-
-2. By the solidification of the liquefied substance upon cooling. Ice
-is a familiar example of this type.
-
-3. By the sublimation of the vapour of the substance, which means the
-direct passage from the vapour to the solid state without traversing
-the usually intervening liquid state. It is usually the most difficult
-of attainment of the four methods; the most familiar instance is snow.
-
-4. By the precipitation of the substance from a solution when set free
-by chemical action.
-
-Other things being equal, the simpler the composition the greater is
-the ease with which a substance may be expected to be formed; for,
-instead of one complex substance, two or more different substances
-may evolve, unless the conditions are nicely arranged. Attempts,
-for instance, to produce beryl might result instead in a mixture of
-chrysoberyl, phenakite, and quartz.
-
-By far the simplest in composition of all the precious stones is
-diamond, which is pure crystallized carbon; but its manufacture is
-attended by well-nigh insuperable difficulties. If carbon be heated
-in air, it burns at a temperature well below its melting point;
-moreover, unless an enormously high pressure is simultaneously applied,
-the product is the other form of crystallized carbon, namely, the
-comparatively worthless graphite. Moissan’s interesting course of
-experiments were in some degree successful, but the tiny diamonds were
-worthless as jewels, and the expense involved in their manufacture was
-out of all proportion to any possible commercial value they might have.
-
-Next to diamond the simplest substances among precious stones are
-quartz (crystallized silica) and corundum (crystallized alumina). The
-crystallization of silica has been effected in several ways, but the
-value in jewellery of quartz, even of the violet variety, amethyst, is
-not such as to warrant its manufacture on a commercial scale. Corundum,
-on the other hand, is held in high esteem; rubies and sapphires, of
-good colour and free from flaws, have always commanded good prices. The
-question of their production by artificial means has therefore more
-than academic interest.
-
-Ever since the year 1837, when Gaudin produced a few tiny flakes,
-French experimenters have steadily prosecuted their researches in the
-crystallization of corundum. Frémy and Feil, in 1877, were the first
-to meet with much success. A portion of one of their crucibles lined
-with glistening ruby flakes is exhibited in the British Museum (Natural
-History).
-
-[Illustration: FIG. 53.—Verneuil’s Inverted Blowpipe.]
-
-In 1885 the jewellery market was completely taken by surprise by the
-appearance of red stones, emanating, so it is alleged, from Geneva;
-having the physical characters of genuine rubies, they were accepted
-as, and commanded the prices of, the natural stones. It was eventually
-discovered that they had resulted from the fusion of a number of
-fragments of natural rubies in the oxy-hydrogen flame. The original
-colour was driven off at that high temperature, but was revived by the
-previous addition of a little bichromate of potassium. Owing to the
-inequalities of growth, the cracks due to rapid cooling, the inclusion
-of air-bubbles, often so numerous as to cause a cloudy appearance,
-and, above all, the unnatural colour, these reconstructed stones, as
-they are termed, were far from satisfactory, but yet they marked such
-an advance on anything that had been accomplished before that for some
-time no suspicion was aroused as to their being other than natural
-stones.
-
-A notable advance in the synthesis of corundum, particularly of ruby,
-was made in 1904, when Verneuil, who had served his apprenticeship
-to science under the guidance of Frémy, invented his ingenious
-inverted form of blowpipe (Fig. 53), which enabled him to overcome the
-difficulties that had baffled earlier investigators, and to manufacture
-rubies vying in appearance after cutting with the best of nature’s
-productions. The blowpipe consisted of two tubes, of which the upper,
-_E_, wide above, was constricted below, and passing down the centre of
-the lower, _F_, terminated just above the orifice of the latter in
-a fine nozzle. Oxygen was admitted at _C_ through the plate covering
-the upper end of the tube, _E_. A rod, which passed through a rubber
-collar in the same plate, supported inside the tube, _E_, a vessel,
-_D_, and at the upper end terminated in a small plate, on which was
-fixed a disc, _B_. The hammer, _A_, when lifted by the action of an
-electromagnet and released, fell by gravity and struck the disc. The
-latter could be turned about a horizontal axis placed eccentrically,
-so that the height through which the hammer fell and the consequent
-force of the blow could be regulated. The rubber collar, which was
-perfectly gas-tight, held the rod securely, but allowed the shocks to
-be transmitted to the vessel, _D_, an arrangement of guides maintaining
-the slight motion of the vessel strictly vertical. This vessel, which
-carried the alumina powder used in the manufacture of the stone, had as
-its base a cylindrical sieve of fine mesh. The succession of rapid taps
-of the hammer caused a regular feed of powder down the tube, the amount
-being regulated by varying the height through which the hammer fell.
-Hydrogen or coal-gas was admitted at _G_ into the outer tube, _F_, and
-in the usual way met the oxygen just above the orifice, _L_. To exclude
-irregular draughts, the flame was surrounded by a screen, _M_, which
-was provided with a mica window, and a water-jacket, _K_, protected the
-upper part of the apparatus from excessive heating.
-
-[Illustration: FIG. 54.—‘Boule,’ or Pear-shaped Drop.]
-
-The alumina was precipitated from a solution of pure ammonia—alum,
-(NH_{4})_{2}SO_{4}.Al_{2}(SO_{4})_{3}.24H_{2}O, in distilled water
-by the addition of pure ammonia, sufficient chrome-alum also being
-dissolved with the ammonia-alum to furnish about 2½ per cent. of
-chromic oxide in the resulting stone. The powder, carefully prepared
-and purified, was placed, as has been stated above, in the vessel,
-_D_, and on reaching the flame at the orifice it melted, and fell
-as a liquid drop, _N_, upon the pedestal, _P_, which was formed of
-previously fused alumina. This pedestal was attached by a platinum
-sleeve to an iron rod, _Q_, which was provided with the necessary screw
-adjustments, _R_ and _S_, for centring and lowering it as the drop
-grew in size. Great care was exercised to free the powder from any
-trace of potassium, which, if present, imparted a brownish tinge to
-the stone. The pressure of the oxygen, low initially both to prevent
-the pedestal from melting, and to keep the area of the drop in contact
-with the pedestal as small as possible, because otherwise flaws tended
-to start on cooling, was gradually increased until the flame reached
-the critical temperature which kept the top of the drop melted, but
-not boiling. The supply of powder was at the same time carefully
-proportioned to the pressure. The pedestal, _P_, was from time to time
-lowered, and the drop grew in the shape of a pear (Fig. 54), the apex
-of which was downwards and adhered to the pedestal by a narrow stalk.
-As soon as the drop reached the maximum size possible with the size of
-the flame, the gases were sharply and simultaneously cut off. After ten
-minutes or so the drop was lowered from the chamber, _M_, by the screw,
-_S_, and when quite cold was removed from the pedestal.
-
-Very few changes have been made in the method when adapted to
-commercial use. Coal-gas has, however, entirely replaced the
-costly hydrogen, and the hammer is operated by a cam instead of an
-electromagnet, while, as may be seen from the view of a gem-stone
-factory (Plate XIV), a number of blowpipes are placed in line so that
-their cams are worked by the same shaft, _a_. The fire-clay screen,
-_b_, surrounding the flame is for convenience of removal divided into
-halves longitudinally, and a small hole is left in front for viewing
-the stone during growth, a red glass screen, _c_, being provided in
-front to protect the eyes from the intense glare. Half the fire-clay
-screen of the blowpipe in the centre of the Plate has been removed to
-show the arrangement of the interior. The centring and the raising
-and lowering apparatus, _d_, have been modified. The process is so
-simple that one man can attend to a dozen or so of these machines, and
-it takes only one hour to grow a drop large enough to be cut into a
-ten-carat stone.
-
-[Illustration: _PLATE XIV_
-
-BLOWPIPE USED FOR THE MANUFACTURE OF RUBIES AND SAPPHIRES]
-
-The drops, unless the finished stone is required to have a similar
-pear shape, are divided longitudinally through the central core into
-halves, which in both shape and orientation are admirably suited to the
-purposes of cutting; as a general rule, the drop splits during cooling
-into the desired direction of its own accord.
-
-[Illustration: FIG. 55.—Bubbles and Curved Striæ in Manufactured Ruby.]
-
-Each drop is a single crystalline individual, and not, as might have
-been anticipated, an alumina glass or an irregular aggregation of
-crystalline fragments, and, if the drop has cooled properly, the
-crystallographic axis is parallel to the core of the pear. The cut
-stone will therefore have not only the density and hardness, but also
-all the optical characters—refractivity, double refraction, dichroism,
-etc.—pertaining to the natural species, and will obey precisely the
-same tests with the refractometer and the dichroscope. Were it not for
-certain imperfections it would be impossible to distinguish between the
-stones formed in Nature’s vast workshop and those produced within the
-confines of a laboratory. The artificial stones, however, are rarely,
-if ever, free from minute air-bubbles (Fig. 55), which can easily be
-seen with an ordinary lens. Their spherical shape differentiates them
-from the plane-sided cavities not infrequently visible in a natural
-stone (Fig. 56). Moreover, the colouring matter varies slightly, but
-imperceptibly, in successive shells, and consequently in the finished
-stone a careful eye can discern the curved striations (Fig. 55)
-corresponding in shape to the original shell. In a natural stone, on
-the other hand, although zones of different colours or varying shades
-are not uncommon, the resulting striations are straight (Fig. 56),
-corresponding to the plane faces of the original crystal form. By
-sacrificing material it might be possible to cut a small stone free
-from bubbles, but the curved striations would always be present to
-betray its origin.
-
-[Illustration: FIG. 56.—Markings in Natural Ruby.]
-
-The success that attended the manufacture of ruby encouraged efforts to
-impart other tints to crystallized alumina. By reducing the percentage
-amount of chromic oxide, pink stones were turned out, in colour not
-unlike those Brazilian topazes, the original hue of which has been
-altered by the application of heat. These artificial stones have
-therefore been called ‘scientific topaz’; of course, quite wrongly,
-since topaz, which is properly a fluo-silicate of aluminium, is quite a
-different substance.
-
-Early attempts made to obtain the exquisite blue tint of the true
-sapphire were frustrated by an unexpected difficulty. The colouring
-matter, cobalt oxide, was not diffused evenly through the drop, but
-was huddled together in splotches, and it was found necessary to add a
-considerable amount of magnesia as a flux before a uniform distribution
-of colour could be secured. It was then discovered that, despite the
-colour, the stones had the physical characters, not of sapphire, but
-of the species closely allied to it, namely, spinel, aluminate of
-magnesium. By an unsurpassable effort of nomenclature these blue stones
-were given the extraordinary name of ‘Hope sapphire,’ from fanciful
-analogy with the famous blue diamond which was once the pride of the
-Hope collection. A blue spinel is occasionally found in nature, but the
-actual tint is somewhat different. These manufactured stones have the
-disadvantage of turning purple in artificial light. By substituting
-lime for magnesia as a flux, Paris, a pupil of Verneuil’s, produced
-blue stones which were not affected to the same extent. The difficulty
-was at length overcome at the close of 1909, when Verneuil, by
-employing as tinctorial agents 0·5 per cent. of titanium oxide and 1·5
-per cent. of magnetic iron oxide, succeeded in producing blue corundum;
-it, however, had not quite the tint of sapphire. Stones subsequently
-manufactured, which were better in colour, contained about 0·12 per
-cent. of titanium oxide, but no iron at all.
-
-By the addition to the alumina of a little nickel oxide and vanadium
-oxide respectively, yellow and yellowish green corundums have been
-obtained. The latter have in artificial light a distinctly reddish
-hue, and have therefore been termed ‘scientific alexandrite’; of
-course, quite incorrectly, since the true alexandrite is a variety of
-chrysoberyl, aluminate of beryllium, a very different substance.
-
-If no colouring matter at all be added and the alum be free from
-potash, colourless stones or white sapphires are formed, which pass
-under the name ‘scientific brilliant.’ It is scarcely necessary to
-remark that they are quite distinct from the true brilliant, diamond.
-
-The high prices commanded by emeralds, and the comparative success that
-attended the reconstruction of ruby from fragments of natural stones,
-suggested that equal success might follow from a similar process with
-powdered beryl, chromic oxide being used as the colouring agent. The
-resulting stones are, indeed, a fair imitation, being even provided
-with flaws, but they are a beryl glass with lower specific gravity and
-refractivity than the true beryl, and are wrongly termed ‘scientific
-emerald.’ Moreover, recently most of the stones so named on the market
-are merely green paste.
-
-It is unfortunate that the real success which has been achieved in the
-manufacture of ruby and sapphire should be obscured by the ill-founded
-claims tacitly asserted in other cases.
-
-At the time the manufactured ruby was a novelty it fetched as much as
-£6 a carat, but as soon as it was discovered that it could easily
-be differentiated from the natural stone, a collapse took place, and
-the price fell abruptly to 30s., and eventually to 5s. and even 1s.
-a carat. The sapphires run slightly higher, from 2s. to 7s. a carat.
-The prices of the natural stones, which at first had fallen, have now
-risen to almost their former level. The extreme disparity at present
-obtaining between the prices of the artificial and the natural ruby
-renders the fraudulent substitution of the one for the other a great
-temptation, and it behoves purchasers to beware where and from whom
-they buy, and to be suspicious of apparently remarkable bargains,
-especially at places like Colombo and Singapore where tourists abound.
-It is no secret that some thousands of carats of manufactured rubies
-are shipped annually to the East. _Caveat emptor._
-
-
-
-
- CHAPTER XV
-
- IMITATION STONES
-
-
-The beryl glass mentioned in the previous chapter marks the transition
-stage between manufactured stones which in all essential characters
-are identical with those found in nature, and artificial stones which
-resemble the corresponding natural stone in outward appearance only. In
-a sense both sorts may be styled artificial, but it would be misleading
-to confound them under the same appellation.
-
-Common paste,[6] which is met with in drapery goods and cheap ornaments
-in general—hat-pins, buckles, and so forth—is composed of ordinary
-crown-glass or flint-glass, the refractive indices being about 1·53 and
-1·63 respectively. The finest quality, which is used for imitations of
-brilliants, is called ‘strass.’ It is a dense lead flint-glass of high
-refraction and strong colour-dispersion, consisting of 38·2 per cent.
-of silica, 53·3 red lead (oxide of lead), and 7·8 potassium carbonate,
-with small quantities of soda, alumina, and other substances. How
-admirable these imitations may be, a study of the windows of a shop
-devoted to such things will show. Unfortunately the addition of
-lead, which is necessary for imparting the requisite refraction and
-‘fire’ to the strass, renders the stones exceedingly soft. All glass
-yields to the file, but strass stones are scratched even by ordinary
-window-glass. If worn in such a way that they are rubbed, they
-speedily lose the brilliance of their polish, and, moreover, they are
-susceptible to attack by the sulphurous fumes present in the smoky air
-of towns, and turn after a time a dirty brown in hue. When coloured
-stones are to be imitated, small quantities of a suitable metallic
-oxide are fused with the glass; cobalt gives rise to a royal-blue tint,
-chromium a ruby red, and manganese a violet. Common paste is not highly
-refractive enough to give satisfactory results when cut as a brilliant,
-and the bases are therefore often coated with quicksilver, or, in the
-case of old jewellery, covered with foil in the setting, in order to
-secure more complete reflection from the interior. The fashioning of
-these imitation stones is easy and cheap. Being moulded, they do not
-require cutting, and the polishing of the facets thus formed is soon
-done on account of the softness of the stones.
-
-A test with a file readily differentiates paste stones from the natural
-stones they pretend to be. Being necessarily singly refractive, they
-are, of course, lacking in dichroism, and their refractivity seldom
-accords even approximately with that of the corresponding natural stone.
-
-In order to meet the test for hardness the doublet was devised. Such
-a stone is composed of two parts—the crown consisting of colourless
-quartz or other inexpensive real and hard stone, and the base being
-made up of coloured glass. When the imitation, say of a sapphire, is
-intended to be more exact, the crown is made of a real sapphire, but
-one deficient in colour, the requisite tint being obtained from the
-paste forming the under part of the doublet. In case the base should
-also be tested for hardness the triplet has been devised. In this the
-base is made of a real stone also, and the coloured paste is confined
-to the girdle section, where it is hidden by the setting. Sapphires and
-emeralds of indifferent colour are sometimes slit across the girdle;
-the interior surfaces are polished, and colouring matter is introduced
-with the cement, generally Canada balsam, which is used to re-unite the
-two portions of the stone together. All such imitations may be detected
-by placing the stone in oil, when the surfaces separating the portions
-of the composite stone will be visible, or the binding cement may be
-dissolved by immersing the stone, if unmounted, in boiling water, or in
-alcohol or chloroform, when the stone will fall to pieces.
-
-The glass imitations of pearls, which have become very common in recent
-years, may, apart from their inferior iridescence, be detected by
-their greater hardness, or by the apparent doubling of, say, a spot of
-ink placed on the surface, owing to reflection from the inner surface
-of the glass shell. They are made of small hollow spheres formed by
-blowing. Next to the glass comes a lining of parchment size, and next
-the under lining, which is the most important part of the imitation,
-consisting of a preparation of fish scales called _Essence d’Orient_,
-When the lining is dry, the globe is filled with hot wax to impart the
-necessary solidity. In cheap imitations the glass balls are not lined
-at all, but merely heated with hydrochloric acid to give an iridescence
-to the surface; sometimes they are coated with wax, which can be
-scraped off with a knife.
-
-
-
-
- PART II—SECTION A
-
- PRECIOUS STONES
-
-
-
-
- CHAPTER XVI
-
- DIAMOND
-
-
-Diamond has held pride of place as chief of precious stones ever
-since the discovery of the form of cutting known as the ‘brilliant’
-revealed to full perfection its amazing qualities; and justly so,
-since it combines in itself extreme hardness, high refraction, large
-colour-dispersion, and brilliant lustre. A rough diamond, especially
-from river gravels, has often a peculiar greasy appearance, and is
-no more attractive to the eye than a piece of washing-soda. It is
-therefore easy to understand why the Persians in the thirteenth century
-placed the pearl, ruby, emerald, and even peridot before it, and
-writers in the Middle Ages frequently esteemed it below emerald and
-ruby. The Indian lapidaries, who were the first to realize that diamond
-could be ground with its own powder, discovered what a wonderful
-difference the removal of the skin makes in the appearance of a stone.
-They, however, made no attempt to shape a stone, but merely polished
-the natural facets, and only added numerous small facets when they
-wished to conceal flaws or other imperfections; indeed, the famous
-traveller, Tavernier, from whom most of our knowledge of early mining
-in India is obtained, invariably found that a stone covered with many
-facets was badly flawed. The full radiant beauty of a diamond comes to
-light only when it is cut in brilliant form.
-
-Of all precious stones diamond has the simplest composition; it is
-merely crystallized carbon, another form of which is the humble and
-useful graphite, commonly known as ‘black-lead.’ Surely nature has
-surpassed all her marvellous efforts in producing from the same element
-substances with such divergent characters as the hard, brilliant, and
-transparent diamond and the soft, dull, and opaque graphite. It is,
-however, impossible to draw any sharp dividing line between the two;
-soft diamond passes insensibly into hard graphite, and vice versa.
-Boart, or bort, as it is sometimes written, is composed of minute
-crystals of diamond arranged haphazardly; it possesses no cleavage,
-its hardness is greater than that of the crystals, and its colour is
-greyish to blackish. Carbon, carbonado, or black diamond, which is
-composed of still more minute crystals, is black and opaque, and is
-perceptibly harder than the crystals. It passes into graphite, which
-varies in hardness, and may have any density between 2·O and 3·O.
-Jewellers apply the term boart to crystals or fragments which are of no
-service as gems; such pieces are crushed to powder and used for cutting
-and polishing purposes.
-
-Diamonds, when absolutely limpid and free from flaws, are said to be
-of the ‘first water,’ and are most prized when devoid of any tinge of
-colour except perhaps bluish (Plate I, Fig. 1). Stones with a slight
-tinge of yellow are termed ‘off-coloured,’ and are far less valuable.
-Those of a canary-yellow colour (Plate I, Fig. 3), however, belong to a
-different category, and have a decided attractiveness. Greenish stones
-also are common, though it is rare to come across one with a really
-good shade of that colour. Brown stones, especially in South Africa,
-are not uncommon. Pink stones are less common, and ruby-red and blue
-stones are rare. Those of the last-named colour have usually what is
-known as a ‘steely’ shade, _i.e._ they are tinged with green; stones of
-a sapphire blue are very seldom met with, and such command high prices.
-
-[Illustration: FIGS. 57—59.—Diamond Crystals.]
-
-Diamond crystallizes (Figs. 57—59 and Plate I, Fig. 2) in octahedra
-with brilliant, smooth faces, and occasionally in cubes with rough
-pitted faces; sometimes three or six faces take the place of each
-octahedron face, and the stone is almost spherical in shape. The
-surfaces of the crystals are often marked with equilateral triangles,
-which are supposed to represent the effects of incipient combustion.
-Twinned crystals, in which the two individuals may be connected by a
-single plane or may be interpenetrating, a star shape often resulting
-in the latter case, are common; sometimes, if of the octahedron type,
-they are beautifully symmetrical. The rounded crystals are frequently
-covered with a peculiar gum-like skin which is somewhat less hard than
-the crystal itself. A large South African stone, weighing 27 grams (130
-carats) and octahedral in shape, which was the gift of John Ruskin,
-and named by him the ‘Colenso’ after the first bishop of Natal, is
-exhibited in the British Museum (Natural History); its appearance is,
-however, marred by its distinctly ‘off-coloured’ tint.
-
-The refraction of diamond is single, but local double refraction is
-common, indicating a state of strain which can often be traced to an
-included drop of liquid carbonic acid; so great is the strain that many
-a fine stone has burst to fragments on being removed from the ground
-in which it has lain. The refractive index for the yellow light of a
-sodium flame is 2·4175, and the slight variation from this mean value
-that has been observed, amounting only to 0·0001, testifies to the
-purity of the composition. The colour-dispersion is large, being as
-much as 0·044, in which respect it surpasses all colourless stones,
-but is exceeded by sphene and the green garnet from the Urals (cf. p.
-217). The lustre of diamond, when polished, is so characteristic as to
-be termed adamantine, and is due to the combination of high refraction
-and extreme hardness. Diamond is translucent to the X (Röntgen) rays;
-it phosphoresces under the action of radium, and of a high-tension
-electric current when placed in a vacuum tube, and sometimes even when
-exposed to strong sunlight. Some diamonds fluoresce in sunlight,
-turning milky, and a few even emit light when rubbed. Crookes found
-that a diamond buried in radium bromide for a year had acquired a
-lovely blue tint, which was not affected even by heating to redness.
-The specific gravity is likewise constant, being 3·521, with a possible
-variation from that mean value of 0·005; but a greater range, as might
-be expected, is found in the impure boart.
-
-Diamond is by far the hardest substance in nature, being marked 10 in
-Mohs’s scale of hardness, but it varies in itself; stones from Borneo
-and New South Wales are so perceptibly harder than those usually in
-the lapidaries’ hands, that they can be cut only with their own and
-not ordinary diamond powder, and some difficulty was experienced in
-cutting them when they first came into the market. It is interesting
-to note that the metal tantalum, the isolation of which in commercial
-amount constituted one of the triumphs of chemistry of recent years,
-has about the same hardness as diamond. Despite its extreme hardness
-diamond readily cleaves under a heavy blow in planes parallel to the
-faces of the regular octahedron, a property utilized for shaping the
-stone previous to cutting it. The fallacious, but not unnatural,
-idea was prevalent up to quite modern times that a diamond would,
-even if placed on an anvil, resist a blow from a hammer: who knows
-how many fine stones have succumbed to this illusory test? The fact
-that diamond could be split was known to Indian lapidaries at the
-time of Tavernier’s visit, and it would appear from De Boodt that in
-the sixteenth century the cleavability of diamond was not unknown in
-Europe, but it was not credited at the time and was soon forgotten.
-Early last century Wollaston, a famous chemist and mineralogist,
-rediscovered the property, and, so it is said, used his knowledge to
-some profit by purchasing large stones, which because of their awkward
-shape or the presence of flaws in the interior were rejected by the
-lapidaries, and selling them back again after cleaving them to suitable
-forms.
-
-It has already been remarked (p. 79) that the interval in hardness
-between diamond and corundum, which comes next to it in Mohs’s scale,
-is enormously greater than that between corundum and the softest of
-minerals. Diamond can therefore be cut only with the aid of its own
-powder, and the cutting of diamond is therefore differentiated from
-that of other stones, the precious-stone trade being to a large extent
-divided into two distinct groups, namely, dealers in diamonds, and
-dealers in all other gem-stones.
-
-The name of the species is derived from the popular form, _adiamentem_,
-of the Latin _adamantem_, itself the alliterative form of the Greek
-ἀδάμας, meaning the unconquerable, in allusion not merely to the
-great hardness but also to the mistaken idea already mentioned. Boart
-probably comes from the Old-French _bord_ or _bort_, bastard.
-
-At the present day diamonds are usually cut as brilliants, though
-the contour of the girdle may be circular, oval, or drop-shaped to
-suit the particular purpose for which the stone is required, or to
-keep the weight as great as possible. Small stones for bordering a
-large coloured stone may also be cut as roses or points. A perfect
-brilliant has 58 facets, but small stones may have not more than 44,
-and exceptionally large stones may with advantage have many more; for
-instance, on the largest stone cut from the Cullinan diamond there are
-no fewer than 74 facets.
-
-The description of the properties of diamond would not be complete
-without a reference to the other valuable, if utilitarian, purposes
-to which it is put. Without its aid much of modern engineering work
-and mining operations would be impossible except at the cost of almost
-prohibitive expenditure of time and money.
-
-Boring through solid rock has been greatly facilitated by the use of
-the diamond drill. For this purpose carbonado or black diamond is more
-serviceable than single crystals, and the price of the former has
-consequently advanced from a nominal figure up to £3 to £12 a carat.
-The actual working part of the drill consists of a cast-steel ring.
-The crown of it has a number of small depressions at regular intervals
-into which the carbonados are embedded. On revolution of the drill an
-annular ring is cut, leaving a solid core which can be drawn to the
-surface. For cooling the drill and for washing away the detritus water
-is pumped through to the working face. The duration of the carbonados
-depends on the nature of the rock and the skill of the operator. The
-most troublesome rock is a sandstone or one with sharp differences in
-hardness, because the carbonados are liable to be torn out of their
-setting. An experienced operator can tell by the feel of the drill the
-nature of the rock at the working face, and by varying the pressure can
-mitigate the risk of damage to the drill.
-
-The tenacity of diamond renders it most suitable for wire-drawing. The
-tungsten filaments used in many of the latest forms of incandescent
-electric lamps are prepared in this manner.
-
-Diamond powder is used for cutting and turning the hardened steel
-employed in modern armaments and for other more peaceful purposes.
-
-Although nearly all the gem-stones scratch glass, diamond alone can be
-satisfactorily employed to cut it along a definite edge. Any flake at
-random will not be suitable, because it will tear the glass and form a
-jagged edge. The best results are given by the junction of two edges
-which do not meet in too obtuse an angle; two edges of the rhombic
-dodecahedron meet the requirements admirably. The stones used by the
-glaziers are minute in size, being not much larger than a pin’s head,
-and thirty of them on an average go to the carat. They are set in
-copper or brass. Some little skill is needed to obtain the best results.
-
-The value of a diamond has always been determined largely by the size
-of the stone, the old rule being that the rate per carat should be
-multiplied by the square of the weight in carats; thus, if the rate be
-£10, the cost of a two-carat stone is four times this sum, or £40, of
-a three-carat stone £90, and so on. For a century, from 1750 to 1850,
-the rate remained almost constant at £4 for rough, £6 for rose-cut,
-and £8 for brilliant-cut diamonds. Since the latter date, owing to
-the increase in the supply of gold, the growth of the spending power
-of the world, and the gradual falling off in the productiveness of
-the Brazilian fields, the rate steadily increased about 10 per cent.
-each year, until in 1865 the rate for brilliants was £18. The rise was
-checked by the discovery of the South African mines; moreover. since
-comparatively large stones are plentiful in these mines, the rule
-of the increase in the price of a stone by the square of its weight
-no longer holds. The rate for the most perfect stones still remains
-high, because such are not so common in the South African mines. The
-classification[7] adopted by the syndicate of London diamond merchants
-who place upon the market the output of the De Beers group of mines is
-as follows:—(_a_) Blue-white, (_b_) white, (_c_) silvery Cape, (_d_)
-fine Cape, (_e_) Cape, (_f_) fine bywater, (_g_) bywater, (_h_) fine
-light brown, (_i_) light brown, (_j_) brown, (_k_) dark brown. Bywaters
-or byes are stones tinged with yellow.
-
-The rate per carat for cut stones in the blue-white and the bywater
-groups is:—
-
- BLUE-WHITE. BYWATER.
- 5-carat stone £40-60 £20-25
- 1 „ 30-40 10-15
- ½ „ 20-25 8-12
- ¼ „ 15-18 6-10
- Mêlée 12-15 5-8
-
-Mêlée are stones smaller than a quarter of a carat. It will be noticed
-that the prices depart largely from the old rule; thus taking the rate
-for a carat blue-white stone, the price of a five-carat stone should
-be from £150-200 a carat, and for a quarter-carat stone only £7, 10s.
-to £10 a carat. There happens to be at the time of writing very little
-demand for five-carat stones. Of course, the prices given are subject
-to constant fluctuation depending upon the supply and demand, and the
-whims of fashion.
-
-
-
-
- CHAPTER XVII
-
- OCCURRENCE OF DIAMOND
-
-
-The whole of the diamonds known in ancient times were obtained from
-the so-called Golconda mines in India. Golconda itself, now a deserted
-fortress near Hyderabad, was merely the mart where the diamonds were
-bought and sold. The diamond-bearing district actually spread over a
-wide area on the eastern side of the Deccan, extending from the Pinner
-River in the Madras Presidency northwards to the Rivers Son and Khan,
-tributaries of the Ganges, in Bundelkhand. The richest mines, where
-the large historical stones were found, are in the south, mostly
-near the Kistna River. The diamonds were discovered in sandstone,
-or conglomerate, or the sands and gravels of river-beds. The mines
-were visited in the middle of the seventeenth century by the French
-traveller and jeweller, Tavernier, when travelling on a commission
-for Louis XIV, and he afterwards published a careful description of
-them and of the method of working them. The mines seem to have been
-exhausted in the seventeenth century; at any rate, the prospecting,
-which has been spasmodically carried on during the last two centuries,
-has proved almost abortive. With the exception of the Koh-i-nor, all
-the large Indian diamonds were probably discovered not long before
-Tavernier’s visit. The diamonds known to Pliny, and in his time, were
-quite small, and it is doubtful if any stones of considerable size came
-to light before A.D. 1000.
-
-India enjoyed the monopoly of supplying the world’s demand for diamonds
-up to the discovery, in 1725, of the precious stone in Brazil. Small
-stones were detected by the miners in the gold washings at Tejuco,
-about eighty miles (129 km.) from Rio de Janeiro, in the Serro do Frio
-district of the State of Minas Geraes. The discovery naturally caused
-great excitement. So many diamonds were found that in 1727 something
-like a slump took place in their value. In order to keep up prices, the
-Dutch merchants, who mainly controlled the Indian output, asserted that
-the diamonds had not been found in Brazil at all, but were inferior
-Indian stones shipped to Brazil from Goa. The tables were neatly turned
-when diamonds were actually shipped from Brazil to Goa, and exported
-thence to Europe as Indian stones. This course and the continuous
-development of the diamond district in Brazil rendered it impossible
-to hoodwink the world indefinitely. The drop in prices was, however,
-stayed by the action of the Portuguese government, who exacted such
-heavy duties and imposed such onerous conditions that finally no one
-would undertake to work the mines. Accordingly, in 1772 diamond-mining
-was declared a royal monopoly in Brazil, and such it remained until
-the severance of Brazil from Portugal in 1834, when private mining was
-permitted by the new government subject to the payment of reasonable
-royalties. The industry was enormously stimulated by the discovery, in
-1844, of the remarkably rich fields in the State of Bahia, especially
-at Serra da Cincorá, where carbonado, or black diamond, first came to
-light, but after a few years, owing to the difficulties of supplying
-labour, the unhealthiness of the climate, and the high cost of living,
-the yield fell off and gradually declined, until the importance of the
-fields was finally eclipsed by the rise of the South African mines.
-The Brazilian mines have proved very productive, but chiefly in small
-diamonds, stones above a carat in weight being few in comparison. The
-largest stone, to which the name, the Star of the South, was applied,
-weighed in the rough 254½ carats; it was discovered at the Bagagem
-mines in 1853. The quality of the diamonds is good, many of them having
-the highly-prized bluish-white colour. The principal diamond-bearing
-districts of Brazil centre at Diamantina, as Tejuco was re-named
-after the discovery of diamonds, Grão Magor, and Bagagem in the State
-of Minas Geraes, at Diamantina in the State of Bahia, and at Goyãz
-and Matto Grosso in the States of the same names. The diamonds occur
-chiefly in _cascalho_, a gravel, containing large masses of quartz
-and small particles of gold, which is supposed to be derived from a
-quartzose variety of micaceous slate known as itacolumite. The mines
-are now to some extent being worked by systematic dredging of the
-river-beds.
-
-Early in 1867 the children of a Boer farmer, Daniel Jacobs, who dwelt
-near Hopetown on the banks of the Orange River, picked up in the course
-of play near the river a white pebble, which was destined not only to
-mark the commencement of a new epoch in the record of diamond mines,
-but to change the whole course of the history of South Africa. This
-pebble attracted the attention of a neighbour, Schalk van Niekerk, who
-suspected that it might be of some value, and offered to buy it. Mrs.
-Jacobs, however, gave it him, laughingly scouting the idea of accepting
-money for a mere pebble. Van Niekerk showed it to a travelling trader,
-by name John O’Reilly, who undertook to obtain what he could for it on
-condition that they shared the proceeds. Every one he met laughed to
-scorn the idea that the stone had any value, and it was once thrown
-away and only recovered after some search in a yard, but at length he
-showed it to Lorenzo Boyes, the Acting Civil Commissioner at Colesberg,
-who, from its extreme hardness, thought it might be diamond and sent
-it to the mineralogist, W. Guybon Atherston, of Grahamstown, for
-determination. So uncertain was Boyes of its value that he did not even
-seal up the envelope containing it, much less register the package.
-Atherston found immediately that the long-scorned pebble was really
-a fine diamond, weighing 21-3/16 carats, and with O’Reilly’s consent
-he submitted it to Sir Philip Wodehouse, Governor at the Cape. The
-latter purchased it at once for £500, and dispatched it to be shown
-at the Paris Exhibition of that year. It did not, however, attract
-much attention; chimerical tales of diamond finds in remote parts of
-the world are not unknown. Indeed, for some time only a few small
-stones were picked up beside the Orange River, and no one believed in
-the existence of any extensive diamond deposit. However, all doubt as
-to the advisibility of prospecting the district was settled by the
-discovery of the superb diamond, afterwards known as the ‘Star of
-South Africa,’ which was picked up in March 1869 by a shepherd boy
-on the Zendfontein farm near the Orange River. Van Niekerk, on the
-alert for news of further discoveries, at once hurried to the spot and
-purchased the stone from the boy for five hundred sheep, ten oxen, and
-a horse, which seemed to the boy untold wealth, but was not a tithe of
-the £11,200 which Lilienfeld Bros., of Hopetown, gave Van Niekerk.
-
-[Illustration: _PLATE XV_
-
-KIMBERLEY MINE, 1871]
-
-[Illustration: _PLATE XVI_
-
-KIMBERLEY MINE, 1872]
-
-This remarkable discovery attracted immediate attention to the
-potentialities of a country which produced diamonds of such a size, and
-prospectors began to swarm into the district, gradually spreading up
-the Vaal River. For some little time not much success was experienced,
-but at length, early in 1870, a rich find was made at Klipdrift,
-now known as Barkly West, which was on the banks of the Vaal River
-immediately opposite the Mission camp at Pniel. The number of miners
-steadily increased until the population on the two sides of the river
-included altogether some four or five thousand people, and there was
-every appearance of stability in the existing order of things. But a
-vast change came over the scene upon the discovery of still richer
-mines lying to the south-east and some distance from the river. The
-ground was actually situated on the route traversed by parties hurrying
-to the Vaal River, but no one dreamed of the wealth that lay under
-their feet. The first discovery was made in August 1870 at the farm
-Jagersfontein, near Fauresmith in Orange River Colony, by De Klerk,
-the intelligent overseer, who noticed in the dry bed of a stream a
-number of garnets, and, knowing that they often accompanied diamond,
-had the curiosity to investigate the point. He was immediately
-rewarded by finding a fine diamond weighing 50 carats. In the following
-month diamonds were discovered about twenty miles from Klipdrift
-at Dutoitspan on the Dorstfontein farm, and a little later also on
-the contiguous farm of Bultfontein; a diamond was actually found in
-the mortar used in the homestead of the latter farm. Early in May
-1871 diamonds were found about two miles away on De Beers’ farm,
-Vooruitzigt, and two months later, in July, a far richer find was made
-on the same farm at a spot which was first named Colesberg Kopje, the
-initial band of prospectors having come from the town of that name
-near the Orange River, but was subsequently known as Kimberley after
-the Secretary of State for the Colonies at that time. Soon a large
-and prosperous town sprang up close to the mines; it rapidly grew
-in size and importance, and to this day remains the centre of the
-diamond-mining industry. Subsequent prospecting proved almost blank
-until the discovery of the Premier or Wesselton mine on Wesselton
-farm, about four miles from Kimberley, in September 1890; it received
-the former name after Rhodes, who was Premier of Cape Colony at that
-date. No further discovery of any importance was made until, in 1902,
-diamonds were found about twenty miles north-west-north of Pretoria in
-the Transvaal, at the new Premier mine, now famed as the producer of
-the gigantic Cullinan diamond.
-
-[Illustration: _PLATE XVII_
-
-KIMBERLEY MINE, 1874]
-
-[Illustration: _PLATE XVIII_
-
-KIMBERLEY MINE, 1881]
-
-The Kimberley mines were at first known as the ‘dry diggings’ on
-account of their arid surroundings in contradistinction to the ‘river
-diggings’ by the Vaal. The dearth of water was at first one of the
-great difficulties in the way of working the former mines, although
-subsequently the accumulation of underground water at lower levels
-proved a great obstacle to the working of the mines. The ‘river
-diggings’ were of a type similar to that met with in India and Brazil,
-the diamonds occurring in a gravelly deposit of limited thickness
-beneath which was barren rock, but the Kimberley mines presented a
-phenomenon hitherto without precedent in the whole history of diamond
-mining. The diamonds were found in a loose surface deposit, which was
-easily worked, and for some time the prospectors thought that the
-underlying limestone corresponded to the bedrock of the river gravel,
-until at length one more curious than his fellows investigated the
-yellowish ground underneath, and found to his surprise that it was even
-richer than the surface layer. Immediately a rush was made back to the
-deserted claims, and the mines were busier than ever. This ‘yellow
-ground,’ as it is popularly called, was much decomposed and easy,
-therefore, to work and sift. About fifty to sixty feet (15-18 m.) below
-the surface, however, it passed into a far harder rock, which from its
-colour is known as the ‘blue ground’; this also, to the unexpected
-pleasure of the miners, turned out to contain diamonds. Difficulties
-arose as each claim, 30 by 30 Dutch feet (about 31 English feet or
-9·45 metres square) in area, was worked downwards. In the Kimberley
-mine (Plate XVI) access to the various claims was secured by retaining
-parallel strips, 15 feet wide, each claim being, therefore, reduced
-in width to 22½ feet, to form roadways running from side to side of
-the mine in one direction. These, however, soon gave way, not only
-because of the falling of the earth composing them, but because they
-were undermined and undercut by the owners of the adjacent claims.
-By the end of 1872 the last roadway had disappeared, and the mine
-presented the appearance of a vast pit. In order to obtain access to
-the claims without intruding on those lying between, and to provide for
-the hauling of the loads of earth to the surface, an ingenious system
-of wire cables in three tiers (Plate XVII) was erected, the lowest
-tier being connected to the outermost claims, the second to claims
-farther from the edge, and the highest to claims in the centre of the
-pit. The mine at that date presented a most remarkable spectacle,
-resembling an enormous radiating cobweb, which had a weird charm by
-night as the moonlight softly illuminated it, and by day, owing to
-the perpetual ring of the flanged wheels of the trucks on the running
-wires, twanged like some gigantic æolian harp. This system fulfilled
-its purpose admirably until, with increasing depth of the workings,
-other serious difficulties arose. Deprived of the support of the hard
-blue ground, the walls of the mine tended to collapse, and additional
-trouble was caused by the underground water that percolated into the
-mine. By the end of 1883 the floor of the Kimberley mine was almost
-entirely covered by falls of ‘reef’ (Plate XVIII), as the surrounding
-rocks are termed, the depth then being about 400 feet (122 m.). In the
-De Beers mine, in spite of the precaution taken to prevent falls of
-reef by cutting the walls of the mine back in terraces, falls occurred
-continuously in 1884, and by 1887, at a depth of 350 feet (107 m.),
-all attempts at open working had to be abandoned. In the Dutoitspan
-mine buttresses of blue ground were left, which held back the reef for
-some years, but ultimately the mine became unsafe, and in March 1886 a
-disastrous fall took place, in which eighteen miners—eight white men
-and ten Kafirs—lost their lives. The Bultfontein mine was worked to the
-great depth of 500 feet (152 m.), but falls occurred in 1889 and put
-an end to open working. In all cases, therefore, the ultimate end was
-the same: the floor of the mine became covered with a mass of worthless
-reef, which rendered mining from above ground dangerous, and, indeed,
-impossible except at prohibitive cost. It was then clearly necessary
-to effect access to the diamond-bearing ground by means of shafts sunk
-at a sufficient distance from the mine to remove any fear of falls of
-reef. For such schemes co-operative working was absolutely essential.
-Plate XIX illustrates the desolate character of the Kimberley mine
-above ground and the vastness of the yawning pit, which is over 1000
-feet (300 m.) in depth.
-
-[Illustration: _PLATE XIX_
-
-KIMBERLEY MINE AT THE PRESENT DAY]
-
-[Illustration: _PLATE XX_
-
-WESSELTON (_open_) MINE]
-
-A certain amount of linking up of claims had already taken place, but,
-although many men must have seen that the complete amalgamation of the
-interests in each mine was imperative, two men alone had the capacity
-to bring their ideas to fruition. C. J. Rhodes was the principal agent
-in the formation in April 1880 of the De Beers Mining Company, which
-rapidly absorbed the remaining claims in the mine, and was re-formed
-in 1887 as the De Beers Consolidated Mining Company. Meantime, Barnett
-Isaacs, better known by the cognomen Barnato, which had been adopted by
-his
-
-brother Henry when engaged in earning his livelihood in the diamond
-fields as an entertainer, had secured the major interests in the
-Kimberley mine. Rhodes saw that, for effective working of the two
-mines by any system of underground working, they must be under one
-management, but to all suggestions of amalgamation Barnato remained
-deaf, and at last Rhodes determined to secure control of the Kimberley
-mine at all costs. The story of the titanic struggle between these
-two men forms one of the epics of finance. Eventually, when shares
-in the Kimberley mine had been boomed to an extraordinary height,
-and the price of diamonds had fallen as low as 18s. a carat, Barnato
-gave way, and in July 1889 the Kimberley mine was absorbed by the De
-Beers Company on payment of the enormous sum of £5,338,650. Shortly
-afterwards they undertook the working of the Dutoitspan and the
-Bultfontein mines, and in January 1896 they acquired the Premier or
-Wesselton mine. The interests in the Jagersfontein mine were in 1888
-united in the New Jagersfontein Mining and Exploration Company, and
-the mine is now worked also by the De Beers Company. Thus, until the
-development of the new Premier mine in the Transvaal, the De Beers
-Company practically controlled the diamond market. The development
-of this last mine was begun so recently, and its size is so vast—the
-longest diameter being half a mile—that open-cut working is likely to
-continue for some years.
-
-[Illustration: _PLATE XXI_
-
-LOADING THE BLUE GROUND ON THE FLOORS, AND PLOUGHING IT OVER]
-
-[Illustration: _PLATE XXII_
-
-WASHING-MACHINES FOR CONCENTRATING THE BLUE GROUND]
-
-Though varying slightly in details, the methods of working the mines
-are identical in principle. From the steeply inclined shaft horizontal
-galleries are run diagonally right across the mine, the vertical
-interval between successive galleries being 40 feet. From each
-gallery side galleries are run at right angles to it and parallel to
-the working face. The blue ground is worked systematically backwards
-from the working face. The mass is stoped, _i.e._ drilled and broken
-from the bottom upwards, until only a thin roof is left. As soon as the
-section is worked out and the material removed, the roof is allowed
-to fall in, and work is begun on the next section of the same level;
-at the same time the first section on the level next below is opened
-out. Thus work is simultaneously carried on in several levels, and a
-vertical plane would intersect the working faces in a straight line
-obliquely inclined to the vertical direction (Fig. 60). When freshly
-mined, the blue ground is hard and compact, but it soon disintegrates
-under atmospheric influence. Indeed, the yellow ground itself was
-merely decomposed blue ground. No immediate attempt is made, therefore,
-to retrieve the precious stones. The blue ground is spread on to
-the ‘floors’ (Plate XXI), _i.e._ spaces of open veldt which have
-been cleared of bushes and inequalities, to the depth of a couple of
-feet, and remains there for periods ranging from six months to two
-years, depending on the quality of the blue ground and the amount of
-rainfall. To hasten the disintegration the blue ground is frequently
-ploughed over and occasionally watered, a remarkable introduction of
-agricultural methods into mining operations. No elaborate patrolling
-or guarding is required, because the diamonds are so sparsely, though
-regularly, scattered through the mass that even of the actual workers
-in the mines but few have ever seen a stone in the blue ground. When
-sufficiently broken up, it is carted to the washing and concentrating
-machines, by means of which the diamonds and the heavier constituents
-are separated from the lighter material.
-
-[Illustration: FIG. 60.—Vertical Section of Diamond Pipe, showing
-Tunnels and Stopes.]
-
-Formerly the diamonds were picked out from the concentrates by means
-of the keen eyes of skilled natives; but the process has been vastly
-simplified and the risk of theft entirely eliminated by the remarkable
-discovery made in 1897 by F. Kirsten, of the De Beers Company, that
-of all the heavy constituents of the blue ground diamond alone, with
-the exception of an occasional corundum and zircon, which are easily
-sorted out afterwards, adheres to grease more readily than to water.
-In this ingenious machine, the ‘jigger’ or ‘greaser’ (Plate XXIII) as
-it is commonly termed, the concentrates are washed over a series of
-galvanized-iron trays, which are covered with a thick coat of grease.
-The trays are slightly inclined downwards, and are kept by machinery
-in constant sideways motion backwards and forwards. So accurate is the
-working of this device that few diamonds succeed in getting beyond
-the first tray, and none progress as far as the third, which is added
-as an additional precaution. The whole apparatus is securely covered
-in so that there is no risk of theft during the operation. The trays
-are periodically removed, and the grease is scraped off and boiled to
-release the diamonds, the grease itself being used over again on the
-trays. This is the first time in the whole course of extraction from
-the mines that the diamonds are actually handled. The stones are now
-passed on to the sorters, who separate them into parcels according to
-their size, shape, and quality.
-
-[Illustration: _PLATE XXIII_
-
-DIAMOND-SORTING MACHINES]
-
-[Illustration: _PLATE XXIV_
-
-KAFIRS PICKING OUT DIAMONDS]
-
-The classification at the mines is first into groups by the shape:
-(1) close goods, (2) spotted stones, (3) rejection cleavage, (4)
-fine cleavage, (5) light brown cleavage, (6) ordinary and rejection
-cleavage, (7) flats, (8) macles, (9) rubbish, (10) boart. Close goods
-are whole crystals which contain no flaws and can be cut into single
-stones. Spotted stones, as their name suggests, contain spots which
-necessitate removal, and cleavage includes stones which are so full of
-flaws that they have to be cleaved or split into two or more stones.
-Flats are distorted octahedra, and macles are twinned octahedra.
-Rubbish is material which can be utilized only for grinding purposes,
-and boart consists of round dark stones which are invaluable for
-rock-drills. These groups are afterwards graded into the following
-subdivisions, depending on increasing depth of yellowish tint: (_a_)
-blue-white, (_b_) first Cape, (_c_) second Cape, (_d_) first bye, (_e_)
-second bye, (_f_) off-colour, (_g_) light yellow, (_h_) yellow. It is,
-however, only the first group that is so minutely subdivided. After
-being purchased, the parcels are split up again somewhat differently
-for the London market (cf. p. 136), and the dealers re-arrange the
-stones according to the purpose for which they are required. Formerly
-a syndicate of London merchants took the whole of the produce of the
-Kimberley mines at a previously arranged price per carat, but at
-the present time the diamonds are sold by certain London firms on
-commission.
-
-The products of each mine show differences in either form or colour
-which enable an expert readily to recognize their origin. The old
-diggings by the Vaal River yielded finer and more colourless stones
-than those found in the dry diggings and the mines underlying them. The
-South African diamonds, taken as a whole, are always slightly yellowish
-or ‘off-coloured’; the mines are, indeed, remarkable for the number of
-fine and large, canary-yellow and brown, stones produced. The Kimberley
-mine yields a fair percentage of white, and a large number of twinned
-and yellow stones. The yield of the De Beers mine comprises mostly
-tinted stones—yellow and brown, occasionally silver capes, and very
-seldom stones free from colour. The Dutoitspan mine is noted for its
-harvest of large yellow diamonds; it also produces fine white cleavage
-and small white octahedra. The stones found in the Bultfontein mine are
-small and spotted, but, on the other hand, the yield has been unusually
-regular. The Premier or Wesselton mine yields a large proportion
-of flawless octahedra, but, above all, a large number of beautiful
-deep-orange diamonds. Of all the South African mines the Jagersfontein
-in the Orange River Colony alone supplies stones of the highly-prized
-blue-white colour and steely lustre characteristic of the old Indian
-stones. The new Premier mine in the Transvaal is prolific, but mostly
-in off-coloured and low-grade stones, the Cullinan diamond being a
-remarkable exception.
-
-To illustrate the amazing productiveness of the South African mines,
-it may be mentioned that, according to Gardner F. Williams, the
-Kimberley group of mines in sixteen years yielded 36 million carats
-of diamonds, and the annual output of the Jagersfontein mine averages
-about a quarter of a million carats, whereas the total output of the
-Brazil mines, for the whole of the long period during which they have
-been worked, barely exceeds 13 million carats. The average yield of the
-South African mines, however, perceptibly diminishes as the depth of
-the mines increases.
-
-The most interesting point connected with the South African diamond
-mines, viewed from the scientific standpoint, is the light that they
-have thrown on the question of the origin of the diamond, which
-previously was an incomprehensible and apparently insoluble problem.
-In the older mines, just as at the river diggings by the Vaal, the
-stones are found in a gravelly deposit that has resulted from the
-disintegration of the rocks through which the adjacent river has
-passed, and it is clear that the diamond cannot have been formed _in
-situ_ here; it had been suspected, and now there is no doubt, that the
-itacolumite rock of Brazil has consolidated round the diamonds which
-are scattered through it, and that it cannot be the parent rock. The
-occurrence at Kimberley is very different. These mines are funnels
-which go downwards to unknown depths; they are more or less oval in
-section, becoming narrower with increasing depth, and are evidently the
-result of some eruptive agency. The Kimberley mine has been worked to
-a depth of nearly 4000 feet (1200 m.), and no signs of a termination
-have as yet appeared. The blue ground which fills these ‘pipes,’ as
-they are termed, must have been forced up from below, since it is
-sharply differentiated from the surrounding country rocks. This blue
-ground is a brecciated peridotite of peculiar constitution, to which
-the well-known petrologist, Carvil Lewis, who made a careful study
-of it, gave the name kimberlite. The blue colour testifies to its
-richness in iron, and it is to the oxidation of the iron constituent,
-that the change of colour to yellow in the upper levels is due. Owing
-to the shafts that have been sunk for working the mines, the nature
-of the surrounding rocks is known to some depth. Immediately below
-the surface is a decomposed ferriferous basalt, about 20 to 90 feet
-(6-27 m.) thick, next a black slaty shale, 200 to 250 feet (60-75 m.)
-thick, then 10 feet (3 m.) of conglomerate, next 400 feet (120 m.)
-of olivine diabase, then quartzite, about 400 feet (120 m.) thick,
-and lastly a quartz porphyry, which has not yet been penetrated. The
-strata run nearly horizontal, and there are no signs of upward bending
-at the pipes. The whole of the country, including the mines, was
-covered with a red sandy soil, and there was nothing to indicate the
-wealth that lay underneath. The action of water had in process of time
-removed all signs of eruptive activity. The principal minerals which
-are associated with diamond in the blue ground are magnetite, ilmenite,
-chromic pyrope, which is put on the market as a gem under the misnomer
-‘Cape-ruby,’ ferriferous enstatite, which also is sometimes cut,
-olivine more or less decomposed, zircon, kyanite, and mica.
-
-The evidence produced by an examination of the blue ground and the
-walls of the pipes proves that the pipes cannot have been volcanoes
-such as Vesuvius. There is no indication whatever of the action of any
-excessive temperature, while, on the other hand, there is every sign of
-the operation of enormous pressure; the diamonds often contain liquid
-drops of carbonic acid. Crookes puts forward the plausible theory that
-steam has been the primary agency in propelling the diamond and its
-associates up into the channel through which it has carved its way to
-freedom, and holds that molten iron has been the solvent for carbon
-which has crystallized out as diamond under the enormous pressures
-obtaining in remote depths of the earth’s crust. It is pertinent to
-note that, by dissolving carbon in molten iron, the eminent chemist,
-Moissan, was enabled to manufacture tiny diamond crystals. Water
-trickling down from above would be immediately converted into steam at
-very high pressure on coming into contact with the molten iron, and, in
-its efforts to escape, the steam would drive the iron and its precious
-contents, together with the adjacent rocks, upwards to the surface. The
-ferriferous nature of the blue ground and the yellow tinge so common
-to the diamonds lend confirmation to this theory. The process by which
-the carbon was extracted from shales or other carboniferous rocks and
-dissolved in iron still awaits elucidation.
-
-Diamonds were found in New South Wales as long ago as 1851 on Turon
-River and at Reedy Creek, near Bathurst, about ninety miles (145 km.)
-from Sydney, but the find was of little commercial importance. A more
-extensive deposit came to light in 1867 farther north at Mudgee. In
-1872 diamonds were discovered in the extreme north of the State, at
-Bingara near the Queensland border. Another discovery was made in 1884
-at Tingha, and still more recently in the tin gravels of Inverell in
-the same region. In their freedom from colour and absence of twinning
-the New South Wales diamonds resemble the Brazilian stones. The average
-size is small, running about five to the carat when cut; the largest
-found weighed nearly 6 carats when cut. They are remarkable for their
-excessive hardness; they can be cut only with their own dust, ordinary
-diamond dust making no impression.
-
-The Borneo diamonds are likewise distinguished by their exceptional
-hardness. They mostly occur by the river Landak, near Pontianak on the
-west coast of the island. They are found in a layer of rather coarse
-gravel, variable, but rarely exceeding a yard (1 m.), in depth, and are
-associated with corundum and rutile, together with the precious metals
-gold and platinum. Indeed, it is no uncommon sight to see natives
-wearing waistcoats ornamented with gold buttons, in each of which a
-diamond is set. The diamonds are well crystallized and generally of
-pure water; yellowish and canary-yellow stones are also common, but
-rose-red, bluish, smoky, and black stones are rare. They seldom exceed
-a carat in weight; but stones of 10 carats in weight are found, and
-occasionally they attain to 20 carats. In 1850 a diamond weighing 77
-carats was discovered. The Rajah of Mattan is said to possess one of
-the purest water weighing as much as 367 carats, but no one qualified
-to pronounce an opinion regarding its genuineness has ever seen it.
-
-In Rhodesia small diamonds have been found in gravel beds resting on
-decomposed granite near the Somabula forest, about 12 miles (19 km.)
-west of Gwelo, in association with chrysoberyl in abundance, blue
-topaz, kyanite, ruby, sapphire, tourmaline, and garnet.
-
-The occurrence of diamond in German South-West Africa is very peculiar.
-Large numbers of small stones are found close to the shore near
-Luderitz Bay in a gravelly surface layer, which is nowhere more than a
-foot in depth. They are picked by hand by natives and washed in sieves.
-In shape they are generally six-faced octahedra or twinned octahedra,
-simple octahedra being rare, and in size they run about four or five
-to the carat, the largest stone as yet found being only 2 carats in
-weight. Their colour is usually yellowish.
-
-Several isolated finds of diamonds have been reported in California
-and other parts of the United States, but none have proved of any
-importance. The largest stone found weighed 23¾ carats uncut; it was
-discovered at Manchester in Virginia.
-
-
-
-
- CHAPTER XVIII
-
- HISTORICAL DIAMONDS
-
-
-The number of diamonds which exceed a hundred carats in weight when
-cut is very limited. Their extreme costliness renders them something
-more than mere ornaments; in a condensed and portable form they
-represent great wealth and all the potentiality for good or ill thereby
-entailed, and have played no small, if sinister, rôle in the moulding
-of history. In bygone days when despotic government was universal, the
-possession of a splendid jewel in weak hands but too often precipitated
-the aggression of a greedy and powerful neighbour, and plunged whole
-countries into the horrors of a ruthless and bloody war. In more
-civilized days a great diamond has often been pledged as security for
-money to replenish an empty treasury in times of stress. The ambitions
-of Napoleon might have received a set-back but for the funds raised
-on the security of the famous Pitt diamond. The history of such
-stones—often one long romance—is full of interest, but space will not
-permit of more than a brief sketch here.
-
-If we except the colossal Cullinan stone, the mines of Brazil and South
-Africa cannot compare with the old mines of India as the birthplace of
-large and perfect diamonds of world-wide fame.
-
-
- (1) KOH-I-NOR
-
-[Illustration: FIG. 61.—Koh-i-nor (top view).]
-
-[Illustration: FIG. 62.—Koh-i-nor (side view).]
-
-The history of the famous stone called the Koh-i-nor, meaning Mound of
-Light, is known as far back as the year 1304, when it fell into the
-hands of the Mogul emperors, and legend even traces it back some four
-thousand years previously. It remained at Delhi until the invasion of
-North-West India by Nadir Shah in 1739, when it passed together with an
-immense amount of spoil into the hands of the conqueror. At his death
-the empire which he had so strenuously founded fell to pieces, and
-the great diamond after many vicissitudes came into the possession of
-Runjit Singh at Lahore. His successors kept it until upon the fall of
-the Sikh power in 1850 it passed to the East India Company, in whose
-name it was presented by Lord Dalhousie to Queen Victoria. At this
-date the stone still retained its original Indian form, but in 1862 it
-was re-cut into the form of a shallow brilliant (Fig. 62), the weight
-thereby being reduced from 186-1/16 to 106-1/16 carats. The wisdom
-of this course has been severely criticized; the stone has not the
-correct shape of a brilliant and is deficient in ‘fire,’ and it has
-with the change in shape lost much of its old historical interest.
-The Koh-i-nor is the private property of the English Royal Family, the
-stone shown in the Tower being a model. It is valued at £100,000.
-
-
- (2) PITT OR REGENT
-
-[Illustration: FIG. 63.—Pitt or Regent (top view).]
-
-[Illustration: FIG. 64.—Pitt or Regent (side view).]
-
-This splendid stone was discovered in 1701 at the famous diamond mines
-at Partial, on the Kistna, about 150 miles (240 km.) from Golconda,
-and weighed as much as 410 carats in the rough. By devious ways it
-came into the hands of Jamchund, a Parsee merchant, from whom it was
-purchased by William Pitt, governor of Fort St. George, Madras, for
-£20,400. On his return to England Pitt had it cut into a perfect
-brilliant (Fig. 63), weighing 163⅞ carats, the operation occupying
-the space of two years and costing £5000; more than £7000 is said to
-have been realized from the sale of the fragments left over. Pitt
-had an uneasy time and lived in constant dread of theft of the stone
-until, in 1717, after lengthy negotiations, he parted with it to the
-Duc d’Orléans, Regent of France, for the immense sum of three and
-three-quarter million francs, about £135,000. With the remainder of the
-French regalia it was stolen from the Garde-meuble on August 17, 1792,
-in the early days of the French Revolution, but was eventually restored
-by the thieves, doubtless because of the impossibility of disposing of
-such a stone, at least intact, and it is now exhibited in the Apollo
-Gallery of the Louvre at Paris. It measures about 30 millimetres in
-length, 25 in width, and 19 in depth, and is valued at £480,000.
-
-
- (3) ORLOFF
-
-[Illustration: FIG. 65.—Orloff (top view).]
-
-[Illustration: FIG. 66.—Orloff (side view).]
-
-One of the finest diamonds existing, this large stone forms the top
-of the imperial sceptre of Russia. It is rose-cut (Fig. 65), the base
-being a cleavage face, and weighs 194¾ carats. It is said to have
-formed at one time one of the eyes of a statue of Brahma which stood
-in a temple on the island of Sheringham in the Cavery River, near
-Trichinopoli, in Mysore, and to have been stolen by a French soldier
-who had somehow persuaded the priests to appoint him guardian of the
-temple. He sold it for £2000 to the captain of an English ship, who
-disposed of it to a Jewish dealer in London for £12,000. It changed
-hands to a Persian merchant, Raphael Khojeh, who eventually sold it to
-Prince Orloff for, so it is said, the immense sum of £90,000 and an
-annuity of £4000. It was presented by Prince Orloff to Catherine II of
-Russia.
-
-
- (4) GREAT MOGUL
-
-This, the largest Indian diamond known, was found in the Kollur mines,
-about the year 1650. Its original weight is said to have been 787½
-carats, but it was so full of flaws that the Venetian, Hortensio
-Borgis, then in India, in cutting it to a rose form reduced its weight
-to 240 carats. It was seen by Tavernier at the time of his visit
-to India, but it has since been quite lost sight of. It has been
-identified with both the Koh-i-nor and the Orloff, and it is even
-suggested that both these stones were cut from it.
-
-
- (5) SANCY
-
-The history of this diamond is very involved, and probably two or more
-stones have been confused. It may have been the one cut by Berquem for
-Charles the Bold, from whose body on the fatal day of Nancy, in 1477,
-it was snatched by a marauding soldier. It was acquired by Nicholas
-Harlai, Seigneur de Sancy, who sold it to Queen Elizabeth at the close
-of the sixteenth century. A hundred years later, in 1695, it was sold
-by James II to Louis XIV. The stone in the French regalia, according
-to the inventory taken in 1791, weighed 53¾ carats. It was never
-recovered after the theft of the regalia in the following year, but
-may be identical with the diamond which was in the possession of the
-Demidoff family and was sold by Prince Demidoff in 1865 to a London
-firm who were said to have been acting for Sir Jamsetjee Jeejeebhoy, a
-wealthy Parsee of Bombay. It was shown at the Paris Exhibition of 1867.
-It was almond-shaped, and covered all over with tiny facets by Indian
-lapidaries.
-
-
- (6) GREAT TABLE
-
-This mysterious stone was seen by Tavernier at Golconda in 1642, but
-has quite disappeared. It weighed 242-3/16 carats.
-
-
- (7) MOON OF THE MOUNTAINS
-
-This diamond is often confused with the Orloff. It was captured by
-Nadir Shah at Delhi, and after his murder was stolen by an Afghan
-soldier who disposed of it to an Armenian, by name Shaffrass. It was
-finally acquired by the Russian crown for an enormous sum.
-
-
- (8) NIZAM
-
-A large diamond, weighing 340 carats, belonged to the Nizam of
-Hyderabad; it was fractured at the beginning of the Indian Mutiny.
-Whether the weight is that previous to fracture or not, there seems to
-be no information.
-
-
- (9) DARYA-I-NOR
-
-This fine diamond, rose-cut and 186 carats in weight, is of the purest
-water and merits its title of ‘River of Light.’ It seems to have been
-captured by Nadir Shah at Delhi, and is now the largest diamond in the
-Persian collection.
-
-
- (10) SHAH
-
-This fine stone, of the purest water, was presented to the Czar
-Nicholas by the Persian prince Chosroes, younger son of Abbas Mirza, in
-1843. At that time it still retained three cleavage faces which were
-engraved with the names of three Persian sovereigns, and weighed 95
-carats. It was, however, subsequently re-cut with the loss of 9 carats,
-and the engraving has disappeared in the process.
-
-
- (11) AKBAR SHAH, OR JEHAN GHIR SHAH
-
-Once the property of the great Mogul, Akbar, this diamond was engraved
-on two faces with Arabic inscriptions by the instructions of his
-successor, Jehan. It disappeared, but turned up again in Turkey
-under the name of ‘Shepherd’s Stone’; it still retained its original
-inscriptions and was thereby recognized. In 1866 it was re-cut, the
-weight being reduced from 116 to 71 carats, and the inscriptions
-destroyed. The stone was sold to the Gaekwar of Baroda for 3½ lakhs of
-rupees (about £23,333).
-
-
- (12) POLAR STAR
-
-A beautiful, brilliant-cut stone, weighing 40 carats, which is known by
-this name, is in the Russian regalia.
-
-
- (13) NASSAK
-
-The Nassak diamond, which weighed 89¾ carats, formed part of the
-Deccan booty, and was put up to auction in London in July 1837. It
-was purchased by Emanuel, a London jeweller, who for £7200 shortly
-afterwards sold it to the Duke of Westminster, in whose family it still
-remains. It was originally pear-shaped, but was re-cut to a triangular
-form with a reduction in weight to 78⅝ carats.
-
-
- (14) NAPOLEON
-
-This diamond was purchased by Napoleon Buonaparte for £8000, and worn
-by him at his wedding with Josephine Beauharnais in 1796.
-
-
- (15) CUMBERLAND
-
-This stone, which weighs 32 carats, was purchased by the city of London
-for £10,000 and presented to the Duke of Cumberland after the battle of
-Culloden; it is now in the possession of the Duke of Brunswick.
-
-
- (16) PIGOTT
-
-A fine Indian stone, weighing 47½ carats, this diamond was brought
-to England by Lord Pigott in 1775 and sold for £30,000. It came into
-the possession of Ali Pacha, Viceroy of Egypt, and was by his orders
-destroyed at his death.
-
-
- (17) EUGÉNIE
-
-This fine stone, weighing 51 carats, was given by the Czarina Catherine
-II of Russia to her favourite, Potemkin. It was purchased by Napoleon
-III as a bridal gift for his bride, and on his downfall was bought by
-the Gaekwar of Baroda.
-
-
- (18) WHITE SAXON
-
-Square in contour, measuring 1-1/12 in. (28 mm.), and weighing 48¾
-carats, this stone was purchased by Augustus the Strong for a million
-thalers (about £150,000).
-
-
- (19) PACHA OF EGYPT
-
-This 40-carat brilliant was purchased by Ibrahim, Viceroy of Egypt, for
-£28,000.
-
-
- (20) STAR OF ESTE
-
-Though a comparatively small stone, in weight 25½ carats, it is noted
-for its perfection of form and quality. It belongs to the Archduke
-Franz Ferdinand of Austrian-Este, eldest son of the Archduke Karl
-Ludwig.
-
-
- (21) TUSCANY, OR AUSTRIAN YELLOW
-
-The beauty of this large stone, 133¾ carats in weight, is marred by
-the tinge of yellow, which is sufficiently pronounced to impair its
-brilliancy; it is a double rose in form. At one time the property of
-the Grand Dukes of Tuscany, it is now in the possession of the Emperor
-of Austria. King mentions a tale that it was bought at a curiosity
-stall in Florence for an insignificant sum, the stone being supposed to
-be only yellow quartz.
-
-
- (22) STAR OF THE SOUTH
-
-This, the largest of the Brazilian diamonds, was discovered at the
-mines of Bagagem in July 1853. Perfectly transparent and without tint,
-it was dodecahedral in shape and weighed 254½ carats, and was sold in
-the rough for £40,000. It was cut as a perfect brilliant, being reduced
-in weight to 125½ carats.
-
-
- (23) ENGLISH DRESDEN
-
-This beautiful stone, which weighed 119½ carats in the rough, was found
-at the Bagagem mines, in Brazil, in 1857, and came into the possession
-of Mr. E. Dresden. It was cut as a long, egg-shaped brilliant, weighing
-76½ carats.
-
-
- (24) STAR OF SOUTH AFRICA
-
-The first considerable stone to be found in South Africa, it was
-discovered at the Vaal River diggings in 1869, and weighed 83½ carats
-in the rough. It was cut to a triangular brilliant of 46½ carats. It
-was finally purchased by the Countess of Dudley for £25,000.
-
-
- (25) STEWART
-
-This large diamond, weighing in the rough 288⅜ carats, was found at the
-Vaal River diggings in 1872, and was first sold for £6000 and shortly
-afterwards for £9000; it was reduced on cutting to 120 carats. Like
-many South African stones, it has a faint yellowish tinge.
-
-
- (26) PORTER-RHODES
-
-This blue-white stone, which weighed 150 carats, was found in a claim
-belonging to Mr. Porter-Rhodes in the Kimberley mine in February 1880.
-
-
- (27) IMPERIAL, VICTORIA, OR GREAT WHITE
-
-This large diamond weighed as much as 457 carats in the rough, and 180
-when cut; it is quite colourless. It was brought to Europe in 1884, and
-was eventually sold to the Nizam of Hyderabad for £20,000.
-
-
- (28) DE BEERS
-
-A pale yellowish stone, weighing 428½ carats, was found in the De Beers
-mine in 1888. It was cut to a brilliant weighing 228½ carats, and
-was sold to an Indian prince. A still larger stone of similar tinge,
-weighing 503¼ carats, was discovered in 1896, and among other large
-stones supplied by the same mine may be mentioned one of 302 carats
-found in 1884, and another of 409 carats found in early years.
-
-
- (29) EXCELSIOR
-
-This, which prior to the discovery of the ‘Cullinan,’ was by far the
-largest South African stone, was found in the Jagersfontein mine on
-June 30, 1893; bluish-white in tint, it weighed 969½ carats. From
-it were cut twenty-one brilliants, the larger stones weighing 67⅞,
-45-13/16, 45-11/16, 39-3/16, 34, 27⅞, 25⅝, 23-11/16, 16-11/32, 13½
-carats respectively, and the total weight of the cut stones amounting
-to 364-3/32 carats.
-
-
- (30) JUBILEE
-
-Another large stone was discovered in the Jagersfontein mine in
-1895. It weighed 634 carats in the rough, and from it was obtained a
-splendid, faultless brilliant weighing 239 carats. It was shown at the
-Paris Exhibition of 1900.
-
-
- (31) STAR OF AFRICA, OR CULLINAN
-
-[Illustration: FIG. 67.—Cullinan No. 1.]
-
-All diamonds pale into insignificance when compared with the colossal
-stone that came to light at the Premier mine near Pretoria in the
-Transvaal on January 25, 1905. It was first called the ‘Cullinan’ after
-Sir T. M. Cullinan, chairman of the Premier Diamond Mine (Transvaal)
-Company, but has recently, by desire of King George V, received the
-name ‘Star of Africa.’ The rough stone weighed 621·2 grams or 3025¾
-carats (about 1⅓ lb.); it displayed three natural faces (Plate XXV)
-and one large cleavage face, and its shape suggested that it was
-a portion of an enormous stone more than double its size; it was
-transparent, colourless, and had only one small flaw near the surface.
-This magnificent diamond was purchased by the Transvaal Government for
-£150,000, and presented to King Edward VII on his birthday, November 9,
-1907.
-
-[Illustration: _PLATE XXV_
-
-CULLINAN DIAMOND
-
-(_Natural size_)]
-
-[Illustration: FIG. 68.—Cullinan No. 2.]
-
-The Cullinan was entrusted to the famous firm, Messrs. I. J. Asscher
-& Co., of Amsterdam, for cutting on January 23, 1908, just three
-years after its discovery. On February 10 it was cleaved into two
-parts, weighing respectively 1977½ and 1040½ carats, from which the
-two largest stones have been cut, one being a pendeloque or drop
-brilliant in shape (Fig. 67) and weighing 516½ carats, and the other
-a square brilliant (Fig. 68) weighing 309-3/16 carats. The first
-has been placed in the sceptre, and the second in the crown of the
-regalia. Besides these there are a pendeloque weighing 92 carats, a
-square-shaped brilliant 62, a heart-shaped stone 18⅜, two marquises
-8-9/16 and 11¼, an oblong stone 6⅝, a pendeloque 4-9/32, and 96 small
-brilliants weighing together 7⅜; the total weight of the cut stones
-amounts to 1036-5/32 carats. The largest stone has 74 and the second 66
-facets. The work was completed and the stones handed to King Edward in
-November 1908.
-
-Although the Premier mine has yielded no worthy compeer of the
-Cullinan, it can, nevertheless, boast of a considerable number of
-large stones which but for comparison with that giant would be thought
-remarkable for their size, no fewer than seven of them having weights
-of over 300 carats, viz. 511, 487¼, 458¾, 391½, 373, 348, and 334
-carats.
-
-
- (32) STAR OF MINAS
-
-This large diamond, which was found in 1911 at the Bagagem mines, Minas
-Geraes, Brazil, had the shape of a dome with a flat base, and weighed
-in the rough 35·875 grams (174¾ carats).
-
- • • • • •
-
-The large stone called the ‘Braganza,’ in the Portuguese regalia, which
-is supposed to be a diamond, is probably a white topaz; it weighs 1680
-carats. The Mattan stone, pear-shaped and weighing 367 carats, which
-was found in the Landak mines near the west coast of Borneo in 1787, is
-suspected to be quartz.
-
-
- COLOURED DIAMONDS
-
-
- (1) HOPE
-
-[Illustration: FIG. 69.—Hope.]
-
-The largest of coloured diamonds, the Hope, weighs 44⅛ carats, and has
-a steely- or greenish-blue, and not the royal-blue colour of the glass
-models supposed to represent it. It is believed to be a portion of a
-drop-form stone (_d’un beau violet_) which was said to have been found
-at the Kollur mines, and was secured by Tavernier in India in 1642 and
-sold by him to Louis XIV in 1668; it then weighed 67 carats. This stone
-was stolen with the remainder of the French regalia in 1792 and never
-recovered. In 1830 the present stone (Fig. 69) was offered for sale
-by Eliason, a London dealer, and was purchased for £18,000 by Thomas
-Philip Hope, a wealthy banker and a keen collector of gems. Probably
-the apex of the original stone had been cut off, reducing it to a
-nearly square stone. The slight want of symmetry of the present stone
-lends confirmation to this view, and two other blue stones are known,
-which, together with the Hope, make up the weight of the original
-stone. At the sale of the Hope collection at Christie’s in 1867 the
-blue diamond went to America. In 1908 the owner disposed of it to Habib
-Bey for the enormous sum of £80,000. It was put up to auction in Paris
-in 1909, and bought by Rosenau, the Paris diamond merchant, for the
-comparatively small sum of 400,000 francs (about £16,000), and was sold
-in January 1911 to Mr. Edward M’Lean for £60,000. The stone is supposed
-to bring ill-luck in its train, and its history has been liberally
-embellished with fable to establish the saying.
-
-
- (2) DRESDEN
-
-A beautiful apple-green diamond, faultless, and of the purest water, is
-contained in the famous Green Vaults of Dresden. It weighs 40 carats,
-and was purchased by Augustus the Strong in 1743 for 60,000 thalers
-(about £9000).
-
-
- (3) PAUL I
-
-A fine ruby-red diamond, weighing 10 carats, is included among the
-Russian crown jewels.
-
-
- (4) TIFFANY
-
-The lovely orange brilliant, weighing 125⅜ carats, which is in the
-possession of Messrs. Tiffany & Co., the well-known jewellers of New
-York, was discovered in the Kimberley mine in 1878.
-
-
-
-
- CHAPTER XIX
-
- CORUNDUM
-
- (_Sapphire_, _Ruby_)
-
-
-Ranking in hardness second to diamond alone, the species known to
-science as corundum and widely familiar by the names of its varieties,
-sapphire and ruby, holds a pre-eminent position among coloured
-gem-stones. The barbaric splendour of ruby (Plate I, Fig. 13) and the
-glorious hue of sapphire (Plate I, Fig. 11) are unsurpassed, and it
-is remarkable that the same species should boast such different, but
-equally magnificent, tints. They, however, by no means exhaust the
-resources of this variegated species. Fine yellow stones (Plate I,
-Fig. 12), which compare with topaz in colour and are its superior in
-hardness, and brilliant colourless stones, which are unfortunately
-deficient in ‘fire’ and cannot therefore approach diamond, are to
-be met with, besides others of less attractive hues, purple, and
-yellowish, bluish, and other shades of green. Want of homogeneity in
-the coloration of corundum is a frequent phenomenon; thus, the purple
-stones on close examination are found to be composed of alternate blue
-and red layers, and stones showing patches of yellow and blue colour
-are common. Owing to the peculiarity of their interior arrangement
-certain stones display when cut _en cabochon_ a vivid six-rayed star of
-light (Plate I, Fig. 15). Sapphire and ruby share with diamond, pearl,
-and emerald the first rank in jewellery. They are popular stones,
-especially in rings; their comparative rarity in large sizes, apart
-from the question of expense, prevents their use in the bigger articles
-of jewellery. The front of the stones is usually brilliant-cut and the
-back step-cut, but Indian lapidaries often prefer to cover the stone
-with a large number of triangular facets, especially if the stone be
-flawed; star-stones are cut more or less steeply _en cabochon_.
-
-In composition corundum is alumina, oxide of aluminium, corresponding
-to the formula Al_{2}O_{3}, but it usually contains in addition small
-quantities, rarely more than 1 per cent., of ferric oxide, chromic
-oxide, and perhaps other metallic oxides. When pure, it is colourless;
-the splendid tints which are its glory have their origin in the minute
-traces of the other oxides present. No doubt chromic oxide is the
-cause of the ruddy hue of ruby, since it is possible, as explained
-above (p. 117), closely to imitate the ruby tint by this means, but
-nothing approaching so large a percentage as 2½ has been detected in
-a natural stone. The blue colour of sapphire may be due to titanic
-oxide, and ferric oxide may be responsible for the yellow hue of
-the ‘oriental topaz,’ as the yellow corundum is termed. Sapphires,
-when of considerable size, are rarely uniform in tint throughout the
-stone. Alternations of blue and red zones, giving rise to an apparent
-purple or violet tint, and the conjunction of patches of blue and
-yellow are common. Perfectly colourless stones are less common, a
-slight bluish tinge being usually noticeable, but they are not in much
-demand because, on account of their lack of ‘fire,’ they are of little
-interest when cut. The tint of the red stones varies considerably in
-depth; jewellers term them, when pale, pink sapphires, but, of course,
-no sharp distinction can be drawn between them and rubies. The most
-highly prized tint is the so-called pigeon’s blood, a shade of red
-slightly inclined to purple. The prices for ruby of good colour run
-from about 25s. a carat for small stones to between £60 and £80 a
-carat for large stones, and still higher for exceptional rubies. The
-taste in sapphires has changed of recent times. Formerly the deep blue
-was most in demand, but now the lighter shade, that resembling the
-colour of corn-flower, is preferred, because it retains a good colour
-in artificial light. Large sapphires are more plentiful than large
-rubies, and prices run lower; even for large perfect stones the rate
-does not exceed £30 a carat. Large and uniform ‘oriental topazes’ are
-comparatively common, and realize moderate prices, about 2s. to 30s.
-a carat according to quality and size. Green sapphires are abundant
-from Australia, but their tint, a kind of deep sage-green, is not very
-pleasing. Brown stones with a silkiness of structure are also known.
-
-The name of the species comes through the French _corindon_ from an
-old Hindu word, _korund_, of unknown significance, and arose from the
-circumstance that the stones which first found their way to Europe came
-from India. At the present day the word corundum is applied in commerce
-to the opaque stones used for abrasive purposes, to distinguish the
-purer material from emery, which is corundum mixed with magnetite and
-other heavy stones of lower hardness. The origin of the word sapphire,
-which means blue, has been discussed in an earlier chapter (p. 110).
-Jewellers use it in a general sense for all corundum except ruby. Ruby
-comes from the Latin _ruber_, red. The prefix ‘oriental’ (p. 111)
-is often used to distinguish varieties of corundum, since it is the
-hardest of ordinary coloured stones and the finest gem-stones in early
-days reached Europe by way of the East.
-
-Corundum crystallizes either in six-sided prisms terminated by flat
-faces (Plate I, Fig. 10), which are often triangularly marked, or with
-twelve inclined faces, six above and six below, meeting in a girdle
-(Plate I, Fig. 14). Ruby favours the former and the other varieties
-the latter type. A fine crystal of ruby—the ‘Edwardes,’ so named by
-the donor, John Ruskin, after Sir Herbert Edwardes—which weighs 33·5
-grams (163 carats), is exhibited in the Mineral Gallery of the British
-Museum (Natural History), and is tilted in such a way that the light
-from a neighbouring window falls on the large basal face, and reveals
-the interesting markings that nature has engraved on it. From its type
-of symmetry corundum is doubly refractive with a direction of single
-refraction running parallel to the edge of the prism. Owing to the
-relative purity of the chemical composition the refractive indices
-are very constant; the ordinary index ranges from 1·766 to 1·774 and
-the extraordinary index from 1·757 to 1·765, the double refraction
-remaining always the same, 0·009. The amount of colour-dispersion is
-small, and therefore colourless corundum displays very little ‘fire.’
-The difference between the indices for red and blue light is, however,
-sufficiently great that the base of a ruby may be left relatively
-thicker than that of a sapphire to secure an equally satisfactory
-effect (cf. p. 98)—a point of some importance to the lapidary, since
-stones are sold by weight and it is his object to keep the weight as
-great as possible. When a corundum is tested on the refractometer in
-white light a wide spectrum deliminates the two portions of the field
-because of the smallness of the colour-dispersion (cf p. 25). The
-dichroism of both ruby and sapphire is marked, the twin colours given
-by the former being red and purplish-red, and by the latter blue and
-yellowish-blue, the second colour in each instance corresponding to
-the extraordinary ray. Tests with the dichroscope easily separate ruby
-and sapphire from any other red or blue stone. This character has an
-important bearing on the proper mode of cutting the stones. The ugly
-yellowish tint given by the extraordinary ray of sapphire should be
-avoided by cutting the stone with its table-facet at right angles to
-the prism edge, which is the direction of single refraction. Whether
-a ruby should be treated in the same way is a moot point. No doubt
-if the colour is deep, it is the best plan, because the amount of
-absorption of light is thereby sensibly reduced, but otherwise the
-delightful nuances distinguishing ruby are best secured by cutting
-the table-facet parallel to the direction of single refraction.
-Yellow corundum also shows distinct dichroism, but by a variation
-more of the depth than of the tint of the colour; the phenomenon is
-faint compared with the dichroic effect of a yellow chrysoberyl. The
-specific gravity also is very constant, varying only from 3·95 to 4·10;
-sapphire is on the whole lighter than ruby. Corundum has the symbol 9
-on Mohs’s scale, but though coming next to diamond it is a very poor
-second (cf. p. 79). As is usually the case, the application of heat
-tends to lighten the colour of the stones: those of a pale violet or
-a yellow colour lose the tint entirely, and the deep violet stones
-turn a lovely rose colour. On the other hand the action of radium has,
-as was shown by Bordas, an intensifying action on the colour, and
-even develops it in a colourless stone. From the latter reaction it
-may be inferred that often in an apparently colourless stone two or
-more selective influences are at work which ordinarily neutralize one
-another, but, being unequally stimulated by the action of radium, they
-thereupon give rise to colour. The stellate appearance of asterias
-or star-stones—star-ruby and star-sapphire—results from the regular
-arrangement either of numerous small channels or of twin-lamellæ in the
-stone parallel to the six sides of the prisms; light is reflected from
-the interior in the form of a six-rayed star (p. 38). Some stones from
-Siam possess a markedly fibrous or silky structure.
-
-The synthetical manufacture of ruby, sapphire, and other varieties of
-corundum has already been described (p. 116).
-
-Besides its use in jewellery corundum is on account of its hardness of
-great service for many other purposes. Small fragments are extensively
-employed for the bearing parts of the movements of watches, and both
-the opaque corundum and the impure kind known as emery are in general
-use for grinding and polishing softer stones, and steel and other
-metal-work.
-
-The world’s supply of fine rubies is drawn almost entirely from the
-famous ruby mines near Mogok, situated about 90 miles (145 km.) in
-a north-easterly direction from Mandalay in Upper Burma and at an
-elevation of about 4000 ft. (1200 m.) above sea-level. It is from this
-district that the stones of the coveted carmine-red, the so-called
-‘pigeon’s blood,’ colour are obtained. The ruby occurs in a granular
-limestone or calcite in association with the spinel of nearly the
-same appearance—the ‘balas-ruby,’ oriental topaz (yellow corundum),
-tourmaline, and occasionally sapphire. Some stones are found in
-the limestone on the sides of the hills, but by far the largest
-quantity occur in the alluvial deposits, both gravel and clay, in the
-river-beds; the ruby ground is locally known as ‘_byon_.’ The stones
-are as a rule quite small, averaging only about four to the carat.
-Before the British annexation of the country in 1885 the mines were a
-monopoly of the Burmese sovereigns and were worked solely under royal
-licence. They are known to be of great antiquity, but otherwise their
-early history is a mystery. It is said that an astute king secured the
-priceless territory in 1597 from the neighbouring Chinese Shans in
-exchange for a small and unimportant town on the Irrawaddy; if that
-be so, he struck an excellent bargain. The mines were allotted to
-licensed miners, _twin-tsas_ (eaters of the mine) as they were called
-in the language of the country, who not only paid for the privilege,
-but were compelled to hand over to the king all stones above a certain
-weight. As might be anticipated this injunction caused considerable
-trouble, and the royal monopolists constantly suspected the miners of
-evading the regulation by breaking up stones of exceptional size; from
-subsequent experience, it is probable that large stones were in reality
-seldom found. Since 1887 the mines have been worked by arrangement with
-the Government of India by the Ruby Mines, Ltd., an English company.
-Its career has been far from prosperous, but during recent years, in
-consequence of the improved methods of working the mines and of the
-more generous terms afterwards accorded by the Government, greater
-success has been experienced; the future is, however, to some extent
-clouded by the advent of the synthetical stone, which has even made its
-way out to the East.
-
-Large rubies are far from common, and such as were discovered in the
-old days were jealously hoarded by the Burmese sovereigns. According to
-Streeter the finest that ever came to Europe were a pair brought over
-in 1875, at a time when the Burmese king was pressed for money. One,
-rich in colour, was originally cushion-shaped and weighed 37 carats;
-the other was a blunt drop in form and weighed 47 carats. Both were cut
-in London, the former being reduced to 32-5/16 carats and the latter
-to 38-9/16 carats, and were sold for £10,000 and £20,000 respectively.
-A colossal stone, weighing 400 carats, is reported to have been found
-in Burma; it was broken into three pieces, of which two were cut and
-resulted in stones weighing 70 and 45 carats respectively, and the
-third was sold uncut in Calcutta for 7 lakhs of rupees (£46,667). The
-finder of another large stone broke it into two parts, which after
-cutting weighed 98 and 74 carats respectively; he attempted in vain to
-evade the royal acquisitiveness, by giving up the larger stone to the
-king and concealing the other. A fine stone, known by the formidable
-appellation of ‘Gnaga Boh’ (Dragon Lord), weighed 44 carats in the
-rough and 20 carats after cutting. Since the mines were taken over
-by the Ruby Mines, Ltd., a few large stones have been discovered. A
-beautiful ruby was found in the Tagoungnandaing Valley, and weighed
-18½ carats in the rough and 11 carats after cutting; perfectly clear
-and of splendid colour, it was sold for £7000, but is now valued at
-£10,000. Another, weighing 77 carats in the rough, was found in 1899,
-and was sold in India in 1904 for 4 lakhs of rupees (£26,667). A stone,
-weighing 49 carats, was discovered in 1887, and an enormous one,
-weighing as much as 304 carats, in 1890.
-
-The ruby, as large as a pigeon’s egg, which is amongst the Russian
-regalia was presented in 1777 to the Czarina Catherine by Gustav III of
-Sweden when on a visit to St. Petersburg. The large red stone in the
-English regalia which was supposed to be a ruby is a spinel (cf p. 206).
-
-Comparatively uncommon as sapphires are in the Burma mines a faultless
-stone, weighing as much as 79½ carats, has been discovered there.
-
-Good rubies, mostly darker in colour than the Burmese stones, are
-found in considerable quantity near Bangkok in Siam, Chantabun
-being the centre of the trade, where, just as in Burma, they are
-intimately associated with the red spinel. Because of the difference
-in tint and the consequent difference in price, jewellers draw a
-distinction between Burma and Siam rubies; but that, of course, does
-not signify any specific difference between them. Siam is, however,
-most distinguished as the original home of splendid sapphires. The
-district of Bo Pie Rin in Battambang produces, indeed, more than
-half the world’s supply of sapphires. In the Hills of Precious
-Stones, such being the meaning of the native name for the locality, a
-number of green corundums are found. Siam also produces brown stones
-characterized by a peculiar silkiness of structure. Rubies are found in
-Afghanistan at the Amir’s mines near Kabul and also to the north of the
-lapis lazuli mines in Badakshan.
-
-The conditions in Ceylon are precisely the converse of those obtaining
-in Burma; sapphire is plentiful and ruby rare in the island. They are
-found in different rocks, sapphire occurring with garnet in gneiss, and
-ruby accompanying spinel in limestone, but they come together in the
-resulting gravels, the principal locality being the gem-district near
-Ratnapura in the south of the island. The largest uncut ruby discovered
-in Ceylon weighed 42½ carats; it had, however, a decided tinge of
-blue in it. Ceylon is also noted for the magnificent yellow corundum,
-‘oriental topaz,’ or, as it is locally called, ‘king topaz,’ which it
-produces.
-
-Beautiful sapphires occur in various parts of India, but particularly
-in the Zanskar range of the north-western Himalayas in the state of
-Kashmir, where they are associated with brown tourmaline. Probably most
-of the large sapphires known have emanated from India. By far the most
-gigantic ever reported is one, weighing 951 carats, said to have been
-seen in 1827 in the treasury of the King of Ava. The collection at the
-Jardin des Plantes contains two splendid rough specimens; one, known as
-the ‘Rospoli,’ is quite flawless and weighs 132-1/16 carats, and the
-other is 2 inches in length and 1½ inches in thickness. The Duke of
-Devonshire possesses a fine cut stone, weighing 100 carats, which is
-brilliant-cut above and step-cut below the girdle. An image of Buddha,
-which is cut out of a single sapphire, is exhibited, mounted on a gold
-pin, in the Mineral Gallery of the British Museum (Natural History).
-
-For some years past a large quantity of sapphires have come into the
-market from Montana, U.S.A., especially from the gem-district about
-twelve miles west of Helena. The commonest colour is a bluish green,
-generally pale, but blue, green, yellow and occasionally red stones are
-also found; they are characterized by their almost metallic lustre.
-With them are associated gold, colourless topaz, kyanite, and a
-beautiful red garnet which is found in grains and usually mistaken for
-ruby. Rubies are also found in limestone at Cowee Creek, North Carolina.
-
-Blue and red corundum, of rather poor quality, has come from the
-Sanarka River, near Troitsk, and from Miask, in the Government of
-Orenburg, Russia, and similar stones have been known at Campolongo, St.
-Gothard, Switzerland.
-
-The prolific gem-district near Anakie, Queensland, supplies examples of
-every known variety of corundum except ruby; blue, green, yellow, and
-parti-coloured stones, and also star-stones, are plentiful. Leaf-green
-corundum is known father south, in Victoria. The Australian sapphire is
-too dark to be of much value.
-
-Small rubies and sapphires are found in the gem-gravels near the
-Somabula Forest, Rhodesia.
-
-
-
-
- CHAPTER XX
-
- BERYL
-
- (_Emerald_, _Aquamarine_, _Morganite_)
-
-
-The species to be considered in this chapter includes the varieties
-emerald and aquamarine, as well as what jewellers understand by beryl.
-It has many incontestable claims on the attention of all lovers of the
-beautiful in precious stones. The peerless emerald (Plate I, Fig. 5),
-which in its verdant beauty recalls the exquisite lawns that grace the
-courts and quadrangles of our older seats of learning, ranks to-day
-as the most costly of jewels. Its sister stone, the lovely aquamarine
-(Plate I, Fig. 4), which seems to have come direct from some mermaid’s
-treasure-house in the depths of a summer sea, has charms not to be
-denied. Pliny, speaking of this species, truly says, “There is not a
-colour more pleasing to the eye”; yet he knew only the comparatively
-inferior stones from Egypt, and possibly from the Ural Mountains.
-Emeralds are favourite ring-stones, and would, no doubt, be equally
-coveted for larger articles of jewellery did not the excessive cost
-forbid, and nothing could be more attractive for a central stone than
-a choice aquamarine of deep blue-green hue. Emeralds are usually
-step-cut, though Indian lapidaries often favour the _en cabochon_
-form; aquamarines, on the other hand, are brilliant-cut in front and
-step-cut at the back.
-
-Beryl, to use the name by which the species is known to science, is
-essentially a silicate of aluminium and beryllium corresponding to the
-formula, Be_{3}Al_{2}(SiO_{3})_{6}. The beryllia is often partially
-replaced by small amounts of the alkaline earths, caesia, potash, soda,
-and lithia, varying from about 1½ per cent. in beryl from Mesa Grande
-to nearly 5 in that from Pala and Madagascar, and over 6, of which 3·6
-is caesia, in beryl from Hebron, Maine; also, as usual, chromic and
-ferric oxides take the place of a little alumina; from 1 to 2 per cent.
-of water has been found in emerald. The element beryllium was, as its
-name suggests, first discovered in a specimen of this species, the
-discovery being made in 1798 by the chemist Vauquelin; it is also known
-as glucinum in allusion to the sweet taste of its salts.
-
-When pure, beryl is colourless, but it is rarely, if ever, free
-from a tinge of blue or green. The colour is usually some shade of
-green—grass-green, of that characteristic tint which is in consequence
-known as emerald-green, or blue-green, yellowish green (Plate I, Fig.
-6), and sometimes yellow, pink, and rose-red. The peculiar colour of
-emerald is supposed to be caused by chromic oxide, small quantities
-of which have been detected in it by chemical analysis; moreover,
-experiment shows that glass containing the same percentage amount of
-chromic oxide assumes the same splendid hue. Emerald, on being heated,
-loses water, but retains its colour unimpaired, which cannot therefore
-be due, as has been suggested, to organic matter. The term aquamarine
-is applied to the deep sea-green and blue-green stones, and jewellers
-restrict the term beryl to paler shades and generally other colours,
-such as yellow, golden, and pink, but Kunz has recently proposed the
-name morganite to distinguish the beautiful rose beryl such as is
-found in Madagascar. The varying shades of aquamarine are due to the
-influence of the alkaline earths modified by the presence of ferric
-oxide or chromic oxide; the beautiful blushing hue of morganite is no
-doubt caused by lithia.
-
-[Illustration: FIG. 70.—Emerald Crystal.]
-
-The name of the species is derived from the Greek βήρυλλος, an ancient
-word, the meaning of which has been lost in the mists of time. The
-Greek word denoted the same species in part as that now understood
-by the name. Emerald is derived from a Persian word which appeared
-in Greek as σμάραγδος, and in Latin as _smaragdus_; it originally
-denoted chrysocolla, or similar green stone, but was transferred upon
-the introduction of the deep-green beryl from Upper Egypt. The name
-aquamarine was suggested by Pliny’s exceedingly happy description of
-the stones “which imitate the greenness of the clear sea,” although it
-was not actually used by him. That emerald and beryl were one species
-was suspected by Pliny, but the identity was not definitely established
-till about a century ago. Morganite is named after John Pierpont Morgan.
-
-The natural crystals have the form of a six-sided prism, and in the
-case of emerald (Fig. 70, and Plate I, Fig. 8) invariably, if whole,
-end in a single face at right angles to the length of the prism;
-aquamarines have in addition a number of small inclined faces, and
-stones from both Russia and Brazil often taper owing to the effects
-of corrosion. The sixfold character of the crystalline symmetry
-necessarily entails that the double refraction, which is small in
-amount, 0·006, is uniaxial in character, and, since the ordinary
-is greater than the extraordinary refractive index, it is negative
-in sign. The values of the indices range between 1·567 and 1·590,
-and 1·572 and 1·598 respectively, in the two cases, the pink beryl
-possessing the highest values. The dichroism is distinct in the South
-American emerald, the twin colours being yellowish and bluish green,
-but otherwise is rather faint. The specific gravity varies between
-2·69 and 2·79, and is therefore a little higher than that of quartz.
-If, therefore, a beryl and a quartz be floating together in a tube
-containing a suitable heavy liquid, the former will always be at a
-sensibly lower level (cf. Fig. 32). The hardness varies from 7½ to
-8, emerald being a little softer than the other varieties. There is
-no cleavage, but like most gem-stones beryl is very brittle, and can
-easily be fractured. Stones rendered cloudy by fissures are termed
-‘mossy.’ When heated before the blowpipe beryl is fusible with
-difficulty; it resists the attack of hydrofluoric acid as well as of
-ordinary acids.
-
-In all probability the whole of the emeralds known in ancient times
-came from the so-called Cleopatra emerald mines in Upper Egypt. For
-some reason they were abandoned, and their position was so completely
-lost that in the Middle Ages it was maintained that emeralds had never
-been found in Egypt at all, but had come from America by way of the
-East. All doubts were set at rest by the re-discovery of the mines
-early last century by Cailliaud, who had been sent by the Viceroy of
-Egypt to search for them. They were, however, not much worked, and
-after a few years were closed again, and were re-opened only about ten
-years ago. The principal mines are at Jebel Zabara and at Jebel Sikait
-in northern Etbai, about 10 miles (16 km.) apart and distant about 15
-miles (24 km.) from the Red Sea, lying in the range of mountains that
-run for a long distance parallel to the west coast of the Red Sea and
-rise to over 1800 feet (550 m.) above sea-level. There are numerous
-signs of considerable, but primitive, workings at distinct periods.
-Both emeralds and beryls are found in micaceous and talcose schists.
-The emeralds are not of very good quality, being cloudy and rather
-light in colour. Finer emeralds have been found in a dark mica-schist,
-together with other beryllium minerals, chrysoberyl and phenakite, and
-also topaz and tourmaline on the Asiatic side of the Ural Mountains,
-near the Takowaja River, which flows into the Bolshoi Reft River, one
-of the larger tributaries of the Pyschma River, about fifty miles (80
-km.) east of Ekaterinburg, a town which is chiefly concerned with the
-mining and cutting of gem-stones. The mine was accidentally discovered
-by a peasant, who noticed a few green stones at the foot of an uprooted
-tree in 1830. Two years later the mine was regularly worked, and
-remained open for twenty years, when it was closed. It has recently
-been re-opened owing to the high rates obtaining for emeralds. Very
-large crystals have been produced here, but in colour they are much
-inferior to the South American stones; small Siberian emeralds, on the
-other hand, are of better colour than small South American emeralds,
-the latter being not so deep in tint. Emeralds have been found in a
-similar kind of schist at Habachtal, in the Salzburg Alps. About thirty
-years ago well-formed green stones were discovered with hiddenite at
-Stony Point, Alexander County, in North Carolina, but not much gem
-material has come to light.
-
-The products of none of the mines that have just been mentioned can
-on the whole compare with the beautiful stones which have come from
-South America. At the time when the Spaniards grimly conquered Peru
-and ruthlessly despoiled the country of the treasures which could be
-carried away, immense numbers of emeralds—some of almost incredible
-size—were literally poured into Spain, and eventually found their
-way to other parts of Europe. These stones were known as Spanish or
-Peruvian emeralds, but in all probability none of them were actually
-mined in Peru. Perhaps the most extraordinary were the five choice
-stones which Cortez presented to his bride, the niece of the Duke de
-Bejar, thereby mortally offending the Queen, who had desired them for
-herself, and which were lost in 1529 when Cortez was shipwrecked on
-his disastrous voyage to assist Charles V at the siege of Algiers.
-All five stones had been worked to divers fantastic shapes. One was
-cut like a bell with a fine pearl for a tongue, and bore on the rim,
-in Spanish, “Blessed is he who created thee.” A second was shaped
-like a rose, and a third like a horn. A fourth was fashioned like a
-fish, with eyes of gold. The fifth, which was the most valuable and
-the most remarkable of all, was hollowed out into the form of a
-cup, and had a foot of gold; its rim, which was formed of the same
-precious metal, was engraved with the words, “Inter natos mulierum non
-surrexit major.” As soon as the Spaniards had seized nearly all the
-emeralds that the natives had amassed in their temples or for personal
-adornment, they devoted their attention to searching for the source
-of these marvels of nature, and eventually in 1558 they lighted by
-accident upon the mines in what is now the United States of Colombia,
-which have been worked almost continuously since that time. Since the
-natives, who naturally resented the gross injustice with which they
-had been treated, and penetrated the greed that prompted the actions
-of the Spaniards, hid all traces of the mines, and refused to give any
-information as to their position, it is possible that other emerald
-mines may yet be found. The present mines are situated near the
-village of Muzo, about 75 miles (120 km.) north-north-west of Bogota,
-the capital of Colombia. The emeralds occur in calcite veins in a
-bituminous limestone of Cretaceous age. The Spaniards formerly worked
-the mines by driving adits through the barren rock on the hillsides to
-the gem-bearing veins, but at the present day the open cut method of
-working is employed. A plentiful supply of water is available, which
-is accumulated in reservoirs and allowed at the proper time to sweep
-the debris of barren rock away into the Rio Minero, leaving the rock
-containing the emeralds exposed. Stones, of good quality, which are
-suited for cutting, are locally known as _canutillos_, inferior stones,
-coarse or ill-shaped, being called _morallons_.
-
-Emerald, unlike some green stones, retains its purity of colour in
-artificial light; in fact, to quote the words of Pliny, “For neither
-sun nor shade, nor yet the light of candle, causeth to change and lose
-their lustre.” Many are the superstitions that have been attached to
-it. Thus it was supposed to be good for the eyes, and as Pliny says,
-“Besides, there is not a gem or precious stone that so fully possesseth
-the eye, and yet never contenteth it with satiety. Nay, if the sight
-hath been wearied and dimmed by intentive poring upon anything else,
-the beholding of this stone doth refresh and restore it again.” The
-idea that it was fatal to the eyesight of serpents appears in Moore’s
-lines—
-
- “Blinded like serpents when they gaze
- Upon the emerald’s virgin blaze.”
-
-The crystals occur attached to the limestone, and are therefore never
-found doubly terminated. The crystal form is very simple, merely a
-hexagonal prism with a flat face at the one end at right angles to it.
-They are invariably flawed, so much so that a flawless emerald has
-passed into proverb as unattainable perfection. The largest single
-crystal which is known to exist at the present day is in the possession
-of the Duke of Devonshire (Fig. 71). In section it is nearly a regular
-hexagon, about 2 inches (51 mm.) in diameter from side to side, and
-the length is about the same; its weight is 276·79 grams (9¾ oz. Av.,
-or 1347 carats). It is of good colour, but badly flawed. It was given
-to the Duke of Devonshire by Dom Pedro of Brazil, and was exhibited
-at the Great Exhibition of 1851. A fine, though much smaller crystal,
-but of even better colour, which weighs 32·2 grams (156½ carats), and
-measures 1⅛ inch (28 mm.) in its widest cross-diameter, and about the
-same in length, was acquired with the Allan-Greg collection by the
-British Museum, and is exhibited in the Mineral Gallery of the British
-Museum (Natural History). The finest cut emerald is said to be one
-weighing 30 carats, which belongs to the Czar of Russia. A small, but
-perfect and flawless, faceted emerald, which is set in a gold hoop, is
-also in the British Museum (Natural History). It is shown, without the
-setting, about actual size, on Plate I, Fig. 5.
-
-[Illustration: FIG. 71.—Duke of Devonshire’s Emerald.
-
-(Natural size.)]
-
-The ever great demand and the essentially restricted supply have forced
-the cost of emeralds of good quality to a height that puts large stones
-beyond the reach of all but a privileged few who have purses deep
-enough. The rate per carat may be anything from £15 upwards, depending
-upon the purity of the colour and the freedom from flaws, but it
-increases very rapidly with the size, since flawless stones of more
-than 4 carats or so in weight are among the rarest of jewels; a perfect
-emerald of 4 carats may easily fetch £1600 to £2000. It seems anomalous
-to say that it has never been easier to procure fine stones than during
-recent years, but the reason is that the high prices prevailing have
-tempted owners of old jewellery to realize their emeralds. On the other
-hand, pale emeralds are worth only a nominal sum.
-
-The other varieties of beryl are much less rare, and, since they
-usually attain to more considerable, and sometimes even colossal, size,
-far larger stones are obtainable. An aquamarine, particularly of good
-deep blue-green colour, is a stone of great beauty, and it possesses
-the merit of preserving its purity of tint in artificial light. It is a
-favourite stone for pendants, brooches, and bracelets, and all purposes
-for which a large blue or green stone is desired. The varying tints are
-said to be due to the presence of iron in different percentages, and
-possibly in different states of oxidation. Unlike emerald, the other
-varieties are by no means so easily recognized by their colour. Blue
-aquamarines may easily be mistaken for topaz, or vice versa, and the
-yellow beryl closely resembles other yellow stones, such as quartz,
-topaz, or tourmaline. Stones which are colourless or only slightly
-tinted command little more than the price of cutting, but the price of
-blue-green stones rapidly advances with increasing depth of tint up
-to £2 a carat. The enormous cut aquamarine which is exhibited in the
-Mineral Gallery of the British Museum (Natural History), affords some
-idea of the great size such stones reach; a beautiful sea-green in
-colour, it weighs 179·5 grams (875 carats), and is table-cut with an
-oval contour.
-
-The splendid six-sided columns which have been discovered in various
-parts of Siberia are among the most striking specimens in any large
-mineral collection. The neighbourhood of Ekaterinburg in the Urals
-is prolific in varieties of aquamarine; especially at Mursinka have
-fine stones been found, in association with topaz, amethyst, and
-schorl, the black tourmaline. Good stones also occur in conjunction
-with topaz at Miask in the Government of Orenburg. It is found in the
-gold-washings of the Sanarka River, in the Southern Urals, but the
-stones are not fitted for service as gems. Magnificent blue-green and
-yellow aquamarines are associated with topaz and smoky quartz in the
-granite of the Adun-Tschilon Mountains, near Nertschinsk, Transbaikal.
-Stones have also been found at the Urulga River in Siberia. Most
-of the bluish-green aquamarines which come into the market at the
-present time have originated in Brazil, particularly in Minas Novas,
-Minas Geraes, where clear, transparent stones, of pleasing colour, in
-various shades, are found in the utmost profusion; beautiful yellow
-stones also occur at the Bahia mines. Aquamarine was obtained in very
-early times in Coimbatore District, Madras, India, and yellow beryl
-comes from Ceylon. Fine blue crystals occur in the granite of the
-Mourne Mountains, Ireland, but they are not clear enough for cutting
-purposes; similar stones are found also at Limoges, Haute Vienne,
-France. Aquamarines of various hues abound in several places in the
-United States, among the principal localities being Stoneham in Maine,
-Haddam in Connecticut, and Pala and Mesa Grande in San Diego County,
-California. The last-named state is remarkable for the numerous stones
-of varying depth of salmon-pink that have been found there. It is,
-however, surpassed by Madagascar, which has recently produced splendid
-stones of perfect rose-red tint and of the finest gem quality, some of
-them being nearly 100 carats in weight. These stones, which have been
-assigned a special name, morganite (cf. _supra_), are associated with
-tourmaline and kunzite. Pink and yellow beryls and deep blue-green
-aquamarines occur in the island in quantity. The pink beryls from
-California are generally pale or have a pronounced salmon tint, and
-seldom approach the real rose-red colour of morganite; one magnificent
-rose-red crystal, weighing nearly 9 lb. (4·05 kg.), has, however, been
-recently discovered in San Diego County, California, and is now in the
-British Museum (Natural History). Blue-green beryl, varying in tint
-from almost colourless to an emerald-green, occurs with tin-stone and
-topaz about 9 miles (14½ km.) north-east of Emmaville in New South
-Wales, Australia.
-
-Probably the largest and finest aquamarine crystal ever seen was one
-found by a miner on March 28, 1910, at a depth of 15 ft. (5 m.) in a
-pegmatite vein at Marambaya, near Arassuahy, on the Jequitinhonha
-River, Minas Geraes, Brazil. It was greenish blue in colour, and a
-slightly irregular hexagonal prism, with a flat face at each end, in
-form; it measured 19 in. (48·5 cm.) in length and 16 in. (41 cm.) in
-diameter, and weighed 243 lb. (110·5 kg.); and its transparency was so
-perfect that it could be seen through from end to end (Plate XXVI). The
-crystal was transported to Bahia, and sold for $25,000 (£5133).
-
-[Illustration: _PLATE XXVI_
-
-LARGE AQUAMARINE CRYSTAL (_one-sixth natural size_), FOUND AT
-MARAMBAYA, MINAS GERAES, BRAZIL]
-
-
-
-
- PART II—SECTION B
-
- SEMI-PRECIOUS STONES
-
-
-
-
- CHAPTER XXI
-
- TOPAZ
-
-
-Topaz is the most popular yellow stone in jewellery, and often
-forms the principal stone in brooches or pendants, especially in
-old-fashioned articles. It is a general idea that all yellow stones
-are topazes, and all topazes are yellow; but neither statement is
-correct. A very large number of yellow stones that masquerade as
-topaz are really the yellow quartz known as citrine. The latter is,
-indeed, almost universally called by jewellers topaz, the qualification
-‘Brazilian’ being used by them to distinguish the true topaz. Many
-species besides those mentioned yield yellow stones. Thus corundum
-includes the beautiful ‘oriental topaz’ or yellow sapphire, and yellow
-tourmalines are occasionally met with; the yellow chrysoberyl always
-has a greenish tinge. Topaz is generally brilliant-cut in front and
-step-cut at the back, and the table facet is sometimes rounded, but
-the colourless stones are often cut as small brilliants; it takes an
-excellent and dazzling polish.
-
-Topaz is a silicate of aluminium corresponding to the formula
-[Al(F,OH)]_{2}SiO_{4}, which was established in 1894 by Penfield and
-Minor as the result of careful research. Contrary to the general
-idea, topaz is usually colourless or very pale in tint. Yellow hues
-of different degrees, from pale to a rich sherry tint (Plate I, Fig.
-9), are common, and pure pale blue (Plate I, Fig. 7) and pale green
-stones, which often pass as aquamarine, are far from rare. Natural,
-red and pink, stones are very seldom to be met with. It is, however, a
-peculiarity of the brownish-yellow stones from Brazil that the colour
-is altered by heating to a lovely rose-pink. Curiously, the tint is not
-apparent when the stone is hot, but develops as it cools to a normal
-temperature; the colour seems to be permanent. Such stones are common
-in modern jewellery. Although the change in colour is accompanied by
-some slight rearrangement of the constituent molecules, since such
-stones are invariably characterized by high refraction and pronounced
-dichroism, the crystalline symmetry, however, remaining unaltered,
-the cause must be attributed to some change in the tinctorial agent,
-probably oxidation. The yellow stones from Ceylon, if treated in a
-similar manner, lose their colour entirely. The pale yellow-brown
-stones from Russia fade on prolonged exposure to strong sunlight, for
-which reason the superb suite of crystals from the Urulga River, which
-came with the Koksharov collection to the British Museum, are kept
-under cover.
-
-The name of the species is derived from _topazion_ (τοπάζειν, to
-seek), the name given to an island in the Red Sea, which in olden
-times was with difficulty located, but it was applied by Pliny and
-his contemporaries to the yellowish peridot found there. The term
-was applied in the Middle Ages loosely to any yellow stone, and was
-gradually applied more particularly to the stone that was then more
-prevalent, the topaz of modern science. As has already been pointed out
-(p. 111), the term is still employed in jewellery to signify any yellow
-stone. The true topaz was probably included by Pliny under the name
-_chrysolithus_.
-
-[Illustration: FIG. 72.—Topaz Crystal.]
-
-The symmetry is orthorhombic, and the crystals are prismatic in shape
-and terminated by numerous inclined faces, and usually by a large
-face perpendicular to the prism edge (Fig. 72). Topaz cleaves with
-great readiness at right angles to the prism edge; owing to its facile
-cleavage, flaws are easily started, and caution must be exercised
-not to damage a stone by knocking it against hard and unyielding
-substances. The dichroism of a yellow topaz is always perceptible,
-one of the twin colours being distinctly more reddish than the other,
-and the phenomenon is very marked in the case of stones the colour of
-which has been artificially altered to pink. The values of the least
-and the greatest of the principal indices of refraction vary from 1·615
-to 1·629, and from 1·625 to 1·637, respectively, the double refraction
-being about 0·010 in amount, and positive in sign. The high values
-correspond to the altered stones. The specific gravity, the mean value
-of which is 3·55 with a variation of 0·05 on either side, is higher
-than would be expected from the refractivity. A cleavage flake exhibits
-in convergent polarized light a wide-angled biaxial picture, the ‘eyes’
-lying outside the field of view. The relation of the principal optical
-directions and the directions of single refraction to the crystal
-are shown in Fig. 27. The hardness is 8 on Mohs’s scale, and in this
-character it is surpassed only by chrysoberyl, corundum, and diamond.
-Topaz is pyro-electric, in which respect tourmaline alone exceeds it,
-and it may be strongly electrified by friction.
-
-Although the range of refraction overlaps that of tourmaline, there
-is no risk of confusion, because the latter has nearly thrice the
-amount of double refraction (cf. p. 29). Apart from the difference in
-refraction, a yellow topaz ought never to be confused with a yellow
-quartz, because the former sinks, and the latter floats in methylene
-iodide. The same test distinguishes topaz from beryl, and, indeed, from
-tourmaline also.
-
-Judged by the criterion of price, topaz is not in the first rank of
-precious stones. Stones of good colour and free from flaws are now,
-however, scarce. Pale stones are worth very little, possibly less than
-4s. a carat, but the price rapidly advances with increase in colour,
-reaching 20s. for yellow, 80s. for pink and blue stones. Since topazes
-are procurable in all sizes customary in jewellery, the rates vary but
-slightly, if at all, with the size.
-
-Topaz occurs principally in pegmatite dykes and in cavities in granite,
-and is interesting to petrologists as a conspicuous instance of the
-result of the action of hot acid vapours upon rocks rich in aluminium
-silicates. Magnificent crystals have come from the extensive mining
-district which stretches along the eastern flank of the Ural Mountains,
-and from the important mining region surrounding Nertschinsk, in the
-Government of Transbaikal, Siberia. Fine green and blue stones have
-been found at Alabashka, near Ekaterinburg, in the Government of Perm,
-and at Miask in the Ilmen Mountains, in the Government of Orenburg.
-Topazes of the rare reddish hue have been picked out from the gold
-washings of the Sanarka River, Troitsk, also in the Government of
-Orenburg. Splendid pale-brown stones have issued from the Urulga River,
-near Nertschinsk, and good crystals have come from the Adun-Tschilon
-Mountains. Kamchatka has produced yellow, blue, and green stones. In
-the British Isles, beautiful sky-blue, waterworn crystals have been
-found at Cairngorm, Banffshire, in Scotland, and colourless stones in
-the Mourne Mountains, Ireland, and at St. Michael’s Mount, Cornwall.
-Most of the topazes used in jewellery of the present day come from
-either Brazil or Ceylon. Ouro Preto, Villa Rica, and Minas Novas, in
-the State of Minas Geraes, are the principal localities in Brazil.
-Numerous stones, often waterworn, brilliant and colourless or tinted
-lovely shades of blue and wine-yellow, occur there; reddish stones also
-have been found at Ouro Preto. Ceylon furnishes a profusion of yellow,
-light-green, and colourless, waterworn pebbles. The colourless stones
-found there are incorrectly termed by the natives ‘water-sapphire,’ and
-the light-green stones are sold with beryl as aquamarines; the stones
-locally known as ‘king topaz’ are really yellow corundum (cf. p. 181).
-Colourless crystals, sometimes with a faint tinge of colour, have
-been discovered in many parts of the world, such as Ramona, San Diego
-County, California, and Pike’s Peak, Colorado, in the United States,
-San Luis Potosi in Mexico, and Omi and Otami-yama in Japan.
-
-
-
-
- CHAPTER XXII
-
- SPINEL
-
- (_Balas-Ruby_, _Rubicelle_)
-
-
-Spinel labours under the serious disadvantage of being overshadowed at
-almost all points by its opulent and more famous cousins, sapphire and
-ruby, and is not so well known as it deserves to be. The only variety
-which is valued as a gem is the rose-tinted stone called balas-ruby
-(Plate XXVII, Fig. 3), which is very similar to the true ruby in
-appearance; they are probably often confused, especially since they
-are found in intimate association in nature. Spinels of other colours
-are not very attractive to the eye, and are not likely to be in much
-demand. Blue spinel (Plate XXVII, Fig. 4) is far from common, but the
-shade is inclined to steely-blue, and is much inferior to the superb
-tint of the true sapphire. Spinel is very hard and eminently suitable
-for a ring-stone, but is seldom large and transparent enough for larger
-articles of jewellery.
-
-Spinel is an aluminate of magnesium corresponding to the formula
-MgAl_{2}O_{4}, and therefore is closely akin to corundum, alumina, and
-chrysoberyl, aluminate of beryllium. The composition may, however,
-vary considerably owing to the isomorphous replacement of one element
-by another; in particular, ferrous oxide or manganese oxide often
-takes the place of some magnesia, and ferric oxide or chromic oxide is
-found instead of part of the alumina. When pure, spinel is devoid of
-colour, but such stones are exceedingly rare. No doubt chromic oxide is
-responsible for the rose-red hue of balas-ruby, and also, when tempered
-by ferric oxide, for the orange tint of rubicelle, and manganese is
-probably the cause of the peculiar violet colour of almandine-spinel.
-It is scarcely possible to define all the shades between blue and red
-that may be assumed by spinel. Stones which are rich in iron are known
-as pleonaste or ceylonite; they are quite opaque, but are sometimes
-used for ornamental wear.
-
-The name of the species comes from a diminutive form of σπῖνος, a
-spark, and refers to the fiery red colour of the most valued kind
-of spinel. It may be noted that the Latin equivalent of the word,
-_carbunculus_, has been applied to the crimson garnet when cut
-_en cabochon_. Balas is derived from _Balascia_, the old name for
-Badakshan, the district from which the finest stones were brought in
-mediæval times.
-
-[Illustration: FIGS. 73, 74.—Spinel Crystals.]
-
-Spinel, like diamond, belongs to the cubic system of crystalline
-symmetry, and occurs in beautiful octahedra, or in flat
-triangular-shaped plates (Figs. 73, 74) the girdles of which are
-cleft at each corner, these plates being really twinned octahedra.
-The refraction is, of course, single, and there is therefore no
-double refraction or dichroism; this test furnishes the simplest
-way of discriminating between the balas and the true ruby. Owing to
-isomorphous replacement the value of the refractive index may lie
-anywhere between 1·716 and 1·736. The lower values, about 1·720,
-correspond to the most transparent red and blue stones; the deep
-violet stones have values above 1·730. Spinel possesses little
-colour-dispersion, or ‘fire.’ In the same way the values of the
-specific gravity, even of the transparent stones, vary between 3·5
-and 3·7, but the opaque ceylonite has values as high as 4·1. Spinel
-is slightly softer than sapphire and ruby, and has the symbol 8 on
-Mohs’s scale, and it is scarcely inferior in lustre to these stones.
-Spinel is easily separated from garnet of similar colour by its lower
-refractivity. Spinels run from 10s. to £5 a carat, depending on their
-colour and quality, and exceptional stones command a higher rate.
-
-Spinel always occurs in close association with corundum. The balas
-and the true ruby are mixed together in the limestones of Burma and
-Siam. Curiously enough, the spinel despite its lower hardness is found
-in the river gravels in perfect crystals, whereas the rubies are
-generally waterworn. Fine violet and blue spinels occur in the prolific
-gem-gravels of Ceylon. A large waterworn octahedron and a rough mass,
-both of a fine red colour, are exhibited in the Mineral Gallery of the
-British Museum (Natural History), and a beautiful faceted blue stone is
-shown close by.
-
-The enormous red stone, oval in shape, which is set in front of the
-English crown, is not a ruby, as it was formerly believed to be,
-but a spinel. It was given to the gallant Black Prince by Pedro the
-Cruel after the battle of Najera in 1367, and was subsequently worn
-by Henry V upon his helmet at the battle of Agincourt. As usual with
-Indian-fashioned stones it is pierced through the middle, but the hole
-is now hidden by a small stone of similar colour.
-
-The British Regalia also contains the famous stone called the Timur
-Ruby or Khiraj-i-Alam (Tribute of the World), which weighs just over
-352 carats, and is the largest spinel-ruby known. It is uncut, but
-polished. Its history goes back to 1398, when it was captured by the
-Amir Timur at Delhi. On the wane of the Tartar empire the stone became
-the property of the Shahs of Persia, until it was given by Abbas I to
-his friend and ally, the Mogul Emperor, Jehangir. It remained at Delhi
-until, on the sack of that city by Nadir Shah in 1739, it, together
-with immense booty, including the Koh-i-nor, fell into the hands of
-the conqueror. Like the great diamond, it eventually came into the
-possession of Runjit Singh at Lahore, and on the annexation of the
-Punjab in 1850 passed to the East India Company. It was shown at the
-Great Exhibition of 1851, and afterwards presented to Queen Victoria.
-
-Mention has been made above (p. 121) of the blue spinel which is
-manufactured in imitation of the true sapphire. The artificial stone is
-quite different in tint from the blue spinel found in nature.
-
-
-
-
- CHAPTER XXIII
-
- GARNET
-
-
-The important group of minerals which are known under the general name
-of garnet provides an apt illustration of the fact that rarity is an
-essential condition if a stone is to be accounted precious. Owing to
-the large quantity of Bohemian garnets, of a not very attractive shade
-of yellowish red, that have been literally poured upon the market
-during the past half-century the species has become associated with
-cheap and often ineffective jewellery, and has acquired a stigma which
-completely prevents its attaining any popularity with those professing
-a nice taste in gem-stones. It must not, however, be supposed that
-garnet has entirely disappeared from high-class jewellery although the
-name may not readily be found in a jeweller’s catalogue. Those whose
-business it is to sell gem-stones are fully alive to the importance of
-a name, and, as has already been remarked (p. 109), they have been fain
-to meet the prejudices of their customers by offering garnets under
-such misleading guises as ‘Cape-ruby,’ ‘Uralian emerald,’ or ‘olivine.’
-
-Garnets may, moreover, figure under another name quite unintentionally.
-Probably many a fine stone masquerades as a true ruby; the
-impossibility of distinguishing these two species in certain cases by
-eye alone is perhaps not widely recognized. An instructive instance
-came under the writer’s notice a few years ago. A lady one day had
-the misfortune to fracture one of the stones in a ruby ring that had
-been in the possession of her family for upwards of a century, and
-was originally purchased of a leading firm of jewellers in London.
-She took the ring to her jeweller, and asked him to have the stone
-replaced by another ruby. A day or two later he sent word that it was
-scarcely worth while to put a ruby in because the stones in the ring
-were paste. Naturally distressed at such an opinion of a ring which had
-always been held in great esteem by her family, the lady consulted a
-friend, who suggested showing it to the writer. A glance was sufficient
-to prove that if the ring had been in use so long the stones could not
-possibly be paste on account of the excellent state of their polish,
-but a test with the refractometer showed that the stones were really
-almandine-garnets, which so often closely resemble the true ruby in
-appearance. Beautiful as the stones were, the ring was probably not
-worth one-tenth what the value would have been had the stones been
-rubies.
-
-To the student of mineralogy garnet is for many reasons of peculiar
-interest. It affords an excellent illustration of the facility which
-certain elements possess for replacing one another without any great
-disturbance of the crystalline form. Despite their apparent complexity
-in composition all garnets conform to the same type of formula: lime,
-magnesia, and ferrous and manganese oxides, and again alumina and
-ferric and chromic oxides may replace each other in any proportion,
-iron being present in two states of oxidation, and it would be rare
-to find a stone which agrees in composition exactly with any of the
-different varieties of garnet given below.
-
-[Illustration: FIGS. 75, 76.—Garnet Crystals.]
-
-Garnet belongs to the cubic system of crystalline symmetry.
-Its crystals are commonly of two kinds, both of which are very
-characteristic, the regular dodecahedron, _i.e._ twelve-faced figure
-(Fig. 75), and the tetrakis-octahedron or three-faced octahedron (Fig.
-76); the latter crystals are, especially when weather- or water-worn,
-almost spherical in shape. Closer and more refined observations have
-shown that garnet is seldom homogeneous, being usually composed of
-several distinct individuals of a lower order of symmetry. Although
-singly refractive as far as can be determined with the refractometer or
-by deviation through a prism, yet when examined under the polarizing
-microscope, garnets display invariably a small amount of local double
-refraction. The transition from light to darkness is, however, not
-sharp as in normal cases, but is prolonged into a kind of twilight.
-In hardness, garnet is on the whole about the same as quartz, but
-varies slightly; hessonite and andradite are a little softer, pyrope,
-spessartite, and almandine are a little harder, while uvarovite is
-almost the same. All the varieties except uvarovite are fusible when
-heated before the blowpipe, and small fragments melt sufficiently on
-the surface in the ordinary bunsen flame to adhere to the platinum
-wire holding them. This test is very useful for separating rough red
-garnets, pyrope or almandine, from red spinels or zircons of very
-similar appearance. Far greater variation occurs in the other physical
-characters. The specific gravity may have any value between 3·55 and
-4·20, and the refractive index ranges between 1·740 and 1·890. Both the
-specific gravity and the refractive index increase on the whole with
-the percentage amount of iron.
-
-Garnet is a prominent constituent of many kinds of rocks, but the
-material most suitable for gem purposes occurs chiefly in crystalline
-schists or metamorphic limestones. Pyrope and demantoid are furnished
-by peridotites and the serpentines resulting from them; almandine and
-spessartite come mostly from granites.
-
-The name of the species is derived from the Latin _granatus_,
-seed-like, and is suggested by the appearance of the spherical crystals
-when embedded in their pudding-like matrix.
-
-The varieties most adapted to jewellery are the fiery-red pyrope and
-the crimson and columbine-red almandine; the closer they approach the
-ruddy hue of ruby the better they are appreciated. Hessonite was at one
-time in some demand, but it inclines too much to the yellowish shade
-of red and possesses too little perfection of transparency to accord
-with the taste of the present day. Demantoid provides beautiful, pale
-and dark emerald-green stones, of brilliant lustre and high dispersion,
-which are admirably adapted for use in pendants or necklaces; on
-account of their comparative softness it would be unwise to risk them
-in rings. In many stones the colour takes a yellowish shade, which
-is less in demand. Uvarovite also occurs in attractive emerald-green
-stones, but unfortunately none as yet have been found large enough for
-cutting. A few truly magnificent spessartites are known—one, a splendid
-example, weighing 6¾ carats, being in the possession of Sir Arthur
-Church; but the species is far too seldom transparent to come into
-general use. The price varies per carat from 2s. for common garnet to
-10s. for stones most akin to ruby in colour, and exceptional demantoids
-may realize even as much as £10 a carat. The old style of cutting was
-almost invariably rounded or _en cabochon_, but at the present day the
-brilliant-cut front and the step-cut back is most commonly adopted.
-
-The several varieties will now be considered in detail.
-
-
- (_a_) HESSONITE
-
- (_Grossular_, _Cinnamon-Stone_, _Hyacinth_, _Jacinth_)
-
-This variety, strictly a calcium-aluminium garnet corresponding to
-the formula Ca_{3}Al_{2}(SiO_{4})_{3}, but generally containing some
-ferric oxide and therefore tending towards andradite, is called by
-several different names. In science it is usually termed grossular, a
-word derived from _grossularia_, the botanical name for gooseberry, in
-allusion to the colour and appearance of many crystals, or hessonite,
-and less correctly essonite, words derived from the Greek ἥσσων
-in reference to the inferior hardness of these stones as compared
-with zircon of similar colour; in jewellery it is better known as
-cinnamon-stone, if a golden-yellow in colour, or hyacinth or jacinth.
-The last word, which is indiscriminately used for hessonite and yellow
-zircon, but should more properly be applied to the latter, is derived
-from an old Indian word (cf. p. 229); jewellers, however, retain it for
-the garnet.
-
-Only the yellow and orange shades of hessonite (Plate XXIX, Fig. 5)
-are used for jewellery. Neither the brownish-green kind, to which the
-term grossular may properly be applied, nor the rose-red is transparent
-enough to serve as a gem-stone. Hessonite may mostly be recognized,
-even when cut, by the curiously granular nature of its structure, just
-as if it were composed of tiny grains imperfectly fused together; this
-appearance, which is very characteristic, may readily be perceived if
-the interior of the stone be viewed through a lens of moderate power.
-
-The specific gravity varies from 3·55 to 3·66, and the refractive index
-from 1·742 to 1·748. The hardness is on the whole slightly below that
-of quartz. When heated before a blowpipe it easily fuses to a greenish
-glass.
-
-The most suitable material is found in some profusion in the
-gem-gravels of Ceylon, in which it is mixed up with zircon of an almost
-identical appearance; both are called hyacinth. Hessonites from other
-localities, although attractive as museum specimens, are not large and
-clear enough for cutting purposes. Switzerland at one time supplied
-good stones, but the supply has long been exhausted.
-
-
- (_b_) PYROPE
-
- (‘_Cape-Ruby_’)
-
-Often quite ruby-red in colour (Plate XXIX, Fig. 6), this variety
-is probably the most popular of the garnets. It is strictly
-a magnesium-aluminium garnet corresponding to the formula
-Mg_{3}Al_{2}(SiO_{4})_{3}, but usually contains some ferrous oxide
-and thus approaches almandine. Both are included among the precious
-garnets. Its name is derived from πυρωπός, fire-like, in obvious
-allusion to its characteristic colour.
-
-Although at its best pyrope closely resembles ruby, its appearance is
-often marred by a tinge of yellow which decidedly detracts from its
-value. Pyrope generally passes as a variety of ruby, and under such
-names as ‘Cape-ruby,’ ‘Arizona-ruby,’ depending on the origin of the
-stones, commands a brisk sale. The specific gravity varies upwards
-from 3·70, depending upon the percentage amount of iron present, and
-similarly the refractive index varies upwards from 1·740; in the higher
-values pyrope merges into almandine. Its hardness is slightly greater
-than that of quartz, and may be expressed on Mohs’s scale by the symbol
-7¼.
-
-An enormous quantity of small red stones, mostly with a slight tinge of
-yellow, have been brought to light at Teplitz, Aussig, and other spots
-in the Bohemian Mittelgebirge, and a considerable industry in cutting
-and marting them has grown up at Bilin. Fine ruby-red stones accompany
-diamond in the ‘blue ground’ of the mines at Kimberley and also at the
-Premier mine in the Transvaal. Similar stones are also found in Arizona
-and Colorado in the United States, and in Australia, Rhodesia, and
-elsewhere.
-
-Although commonly quite small in size, pyrope has occasionally attained
-to considerable size. According to De Boodt the Kaiser Rudolph II had
-one in his possession valued at 45,000 thalers (about £6750). The
-Imperial Treasury at Vienna contains a stone as large as a hen’s egg.
-Another about the size of a pigeon’s egg is in the famous Green Vaults
-at Dresden, and the King of Saxony has one, weighing 468½ carats, set
-in an Order of the Golden Fleece.
-
-
- (_c_) RHODOLITE
-
-This charming pale-violet variety was found at Cowee Creek and at
-Mason’s Branch, Macon County, North Carolina, U.S.A., but in too
-limited amount to assume the position in jewellery it might otherwise
-have expected. In composition it lies between pyrope and almandine,
-and may be supposed to contain a proportion of two molecules of the
-former to one of the latter. Its specific gravity is 3·84, refractive
-index 1·760, and hardness 7¼. It exhibits in the spectroscope the
-absorption-bands characteristic of almandine.
-
-
- (_d_) ALMANDINE
-
- (_Carbuncle_)
-
-This variety is iron-aluminium garnet corresponding to the formula
-Fe_{3}Al_{2}(SiO_{4})_{3}, but the composition is very variable. In
-colour it is deep crimson and violet or columbine-red (Plate XXIX, Fig.
-8), but with increasing percentage amount of ferric oxide it becomes
-brown and black, and opaque, and quite unsuitable for jewellery. The
-name of the variety is a corruption of Alabanda in Asia Minor, where
-in Pliny’s time the best red stones were cut. Almandine is sometimes
-known as Syriam, or incorrectly Syrian garnet, because at Syriam, once
-the capital of the ancient kingdom of Pegu, which now forms part of
-Lower Burma, such stones were cut and sold. Crimson stones, cut in the
-familiar _en cabochon_ form and known as carbuncles, were extensively
-employed for enriching metalwork, and a half-century or so ago were
-very popular for ornamental wear, but their day has long since gone.
-Such glowing stones are aptly described by their name, which is derived
-from the Latin _carbunculus_, a little spark. In Pliny’s time, however,
-the term was used indiscriminately for all red stones. It has already
-been remarked that the word spinel has a similar significance.
-
-The specific gravity varies from 3·90 for transparent stones to 4·20
-for the densest black stones, and the refractive index may be as high
-as 1·810. Almandine is one of the hardest of the garnets, and is
-represented by the symbol 7½ on Mohs’s scale. The most interesting and
-curious feature of almandine lies in the remarkable and characteristic
-absorption-spectrum revealed when the transmitted light is examined
-with a spectroscope (p. 61). The phenomenon is displayed most vividly
-by the violet stones, and is, indeed, the cause of their peculiar
-colour.
-
-Although a common mineral, almandine of a quality fitted for jewellery
-occurs in comparatively few localities. It is found in Ceylon, but
-not so plentifully as hessonite. Good stones are mined in various
-parts of India, and are nearly all cut at Delhi or Jaipur. Brazil
-supplies good material, especially in the Minas Novas district of
-Minas Geraes, where it accompanies topaz, and Uruguay also furnishes
-serviceable stones. Almandine is found in Australia, and in many parts
-of the United States. Recently small stones of good colour have been
-discovered at Luisenfelde in German East Africa.
-
-
- (_e_) SPESSARTITE
-
-Properly a manganese-aluminium garnet corresponding to the formula
-Mn_{3}Al_{2}(SiO_{4})_{3}, this variety generally contains iron in
-both states of oxidation. If only transparent and large enough its
-aurora-red colour would render it most acceptable in jewellery. Two
-splendid stones have, indeed, been found in Ceylon (p. 211), and good
-stones rather resembling hessonites have been quarried at Amelia
-Court House in Virginia, and others have come from Nevada; otherwise,
-spessartite is unknown as a gem-stone.
-
-The specific gravity ranges from 4·0 to 4·3, and the refractive index
-is about 1·81, both characters being high; the hardness is slightly
-greater than that of quartz.
-
-
- (_f_) ANDRADITE
-
- (_Demantoid_, _Topazolite_, ‘_Olivine_’)
-
-Andradite is strictly a calcium-iron garnet corresponding to the
-formula Ca_{3}Fe_{2}(SiO_{4})_{3}, but as usual the composition varies
-considerably. It is named after d’Andrada, a Portuguese mineralogist,
-who made a study of garnet more than a century ago.
-
-Once contemptuously styled common garnet, andradite suddenly sprang
-into the rank of precious stones upon the discovery some thirty
-years ago of the brilliant, green stones (Plate XXIX, Fig. 7) in the
-serpentinous rock beside the Bobrovka stream, a tributary of the
-Tschussowaja River, in the Sissersk district on the western side of
-the Ural Mountains. The shade of green varies from olive through
-pistachio to a pale emerald, and is probably due to chromic oxide. Its
-brilliant lustre, almost challenging that of diamond, and its enormous
-colour-dispersion, in which respect it actually transcends diamond,
-raise it to a unique position among coloured stones. Unfortunately
-its comparative softness limits it to such articles of jewellery as
-pendants and necklaces, where it is not likely to be rubbed. When first
-found it was supposed to be true emerald, which does actually occur
-near Ekaterinburg, and was termed ‘Uralian emerald.’ When analysis
-revealed its true nature, it received from science the slightly
-inharmonious name of demantoid in compliment to its adamantine lustre.
-Jewellers, however, prefer to designate it ‘olivine,’ not very happily,
-because the stones usually cut are not olive-green and the name is
-already in extensive use in science for a totally distinct species (p.
-225); they recognized the hopelessness of endeavouring to find a market
-for them as garnets. The yellow kind of andradite known as topazolite
-would be an excellent gem-stone if only it were found large and
-transparent enough. Ordinary andradite is brown or black, and opaque;
-it has occasionally been used for mourning jewellery.
-
-The specific gravity varies from 3·8 to 3·9, being about 3·85 for
-demantoid, which has a high refractive index, varying from 1·880 to
-1·890, and may with advantage be cut in the brilliant form. It is the
-softest of the garnets, being only 6½ on Mohs’s scale.
-
-
- (_g_) UVAROVITE
-
-This variety, which is altogether unknown in jewellery, is
-a calcium-iron garnet corresponding mainly to the formula
-Ca_{3}Cr_{2}(SiO_{4})_{3}, but with some alumina always present, and
-was named after a Russian minister. It has an attractive green colour,
-and is, moreover, hard, being about on Mohs’s scale, but it has never
-yet come to light of a size suitable for cutting. The specific gravity
-is low, varying from 3·41 to 3·52. Unlike the kindred varieties it
-cannot be fused by heating before an ordinary blowpipe.
-
-
-
-
- CHAPTER XXIV
-
- TOURMALINE
-
- (_Rubellite_)
-
-
-Tourmaline is unsurpassed even by corundum in variety of hue, and
-it has during recent years rapidly advanced in public favour,
-mainly owing to the prodigal profusion in which nature has formed
-it in that favoured State, California, the garden of the west. Its
-comparative softness militates against its use in rings, but its
-gorgeous coloration renders it admirably fitted for service in any
-article of jewellery, such as a brooch or a pendant, in which a large
-central stone is required. Like all coloured stones it is generally
-brilliant-cut in front and step-cut at the back, but occasionally it is
-sufficiently fibrous in structure to display, when cut _en cabochon_,
-pronounced chatoyancy.
-
-The composition of this complex species has long been a vexed
-question among mineralogists, but considerable light was
-recently thrown on the subject by Schaller, who showed that all
-varieties of tourmaline may be referred to a formula of the type
-12SiO_{2}.3B_{2}O_{3}.(9-_x_)[(Al,Fe)_{2}O_{3}].3_x_[(Fe,Mn,Ca,
-Mg,K_{2},Na_{2},Li_{2},H_{2})O].3H_{2}O. The ratios of boric oxide,
-silica, and water are nearly constant in all analyses, but great
-variation is possible in the proportions of the other constituents.
-Having regard to this complexity, it is not surprising to find that
-the range in colour is so great. Colourless stones, to which the name
-achroite is sometimes given, were at one time exceedingly rare, but
-they are now found in greater number in California. Stones which are
-most suited to jewellery purposes are comparatively free from iron, and
-apparently owe their wonderful tints to the alkaline earths; lithia,
-for instance, is responsible for the beautiful tint of the highly
-prized rubellite, and magnesia, no doubt, for the colour of the brown
-stones of various tints. Tourmaline rich in iron is black and almost
-opaque. It is a striking peculiarity of the species that the crystals
-are rarely uniform in colour throughout, the boundaries between the
-differently coloured portions being sharp and abrupt, and the tints
-remarkably in contrast. Sometimes the sections are separated by planes
-at right angles to the length of the crystal, and sometimes they are
-zonal, bounded by cylindrical surfaces running parallel to the same
-length. In the latter case a section perpendicular to the length shows
-zones of at least three contrasting tints. In the Brazilian stones the
-core is generally red, bounded by white, with green on the exterior,
-while the reverse is the case in the Californian stones, the core being
-green or yellow, bounded by white, with red on the exterior. Tourmaline
-may, indeed, be found of almost every imaginable tint, except,
-perhaps, the emerald green and the royal sapphire-blue. The principal
-varieties are rose-red and pink (rubellite) (Plate XXVII, Fig. 1),
-green (Brazilian emerald), indigo-blue (indicolite), blue (Brazilian
-sapphire), yellowish green (Brazilian peridot) (Plate XXVII, Fig. 2),
-honey-yellow (Ceylonese peridot), violet-red (siberite), and brown
-(Plate XXVII, Fig. 8). The black, opaque stones are termed schorl.
-
-The name of the species is derived from the Ceylonese word, _turamali_,
-and was first employed when a parcel of gem-stones was brought to
-Amsterdam from Ceylon in 1703; in Ceylon, however, the term is applied
-by native jewellers to the yellow zircon commonly found in the island.
-Schorl, the derivation of which is unknown, is the ancient name for the
-species, and is still used in that sense by miners, but it has been
-restricted by science to the black variety. The ‘Brazilian emerald’
-was introduced into Europe in the seventeenth century and was not
-favourably received, possibly because the stones were too dark in
-colour and were not properly cut; that they should have been confused
-with the true emerald is eloquent testimony to the extreme ignorance
-of the characters of gem-stones prevalent in those dark ages. Achroite
-comes from the Greek, ἄχροος, without colour.
-
-[Illustration: FIG. 77.—Tourmaline Crystal.]
-
-To the crystallographer tourmaline is one of the most interesting of
-minerals. If the crystals, which are usually prismatic in form, are
-doubly terminated, the development is so obviously different at the
-two ends (Fig. 77) as to indicate that directional character in the
-molecular arrangement, termed the polarity, which is borne out by other
-physical properties. Tourmaline is remarkably dichroic, A brown stone,
-except in very thin sections, is practically opaque to the ordinary
-ray, and consequently a section cut parallel to the crystallographic
-axis, _i.e._ to the length of a crystal prismatically developed,
-transmits only the extraordinary ray. Such sections were in use for
-yielding plane-polarized light before Nicol devised the calcite prism
-known by his name (cf. p. 44). It is evident that tourmaline, unless
-very light in tint, must be cut with the table facet parallel to that
-axis, because otherwise the stone will appear dark and lifeless. The
-values of the extraordinary and ordinary refractive indices range
-between 1·614 and 1·638, and 1·633 and 1·669 respectively; the double
-refraction, therefore, is fairly large, amounting to 0·025, and,
-since the ordinary exceeds the extraordinary ray, its character is
-negative. The specific gravity varies from 3·0 to 3·2. The lower values
-in both characters correspond to the lighter coloured stones used in
-jewellery; the black stones, as might be expected from their relative
-richness in iron, are the densest. The hardness is only about the same
-as that of quartz, or perhaps a little greater, varying from 7 to 7½.
-It will be noticed that the range of refractivity overlaps that of
-topaz (_q.v._) but the latter has a much smaller double refraction,
-and may thus be distinguished (p. 29). Unmounted stones are still more
-easily distinguished, because tourmaline floats in methylene iodide,
-while topaz sinks. The pyro-electric phenomenon (cf. p. 82) for which
-tourmaline is remarkable, although of little value as a test in the
-case of a cut stone, is of great scientific interest, because it is
-strong evidence of the peculiar crystalline symmetry pertaining to its
-molecular arrangement. Tourmalines range in price from 5s. to 20s. a
-carat according to their colour and quality, but exceptional stones may
-command a higher rate.
-
-Tourmaline is usually found in the pegmatite dykes of granites, but
-it also occurs in schists and in crystalline limestones. Rubellite
-is generally associated with the lithia mica, lepidolite; the groups
-of delicate pink rubellite bespangling a background of greyish
-white lepidolite are among the most beautiful of museum specimens.
-Magnificent crystals of pink, blue, and green tourmaline have been
-found in the neighbourhood of Ekaterinburg, principally at Mursinka, in
-the Urals, Russia, and fine rubellite has come from the Urulga River,
-and other spots near Nertschinsk, Transbaikal, Asiatic Russia. Elba
-produces pink, yellowish, and green stones, frequently particoloured;
-sometimes the crystals are blackened at the top, and are then known
-locally as ‘nigger-heads.’ Ceylon supplies small yellow stones—the
-original tourmaline—which are confused with the zircon of a similar
-colour, and rubellite accompanies the ruby at Ava, Burma. Beautiful
-crystals, green and red, often diversely coloured, come from various
-parts, such as Minas Novas and Arassuahy, of the State of Minas Geraes,
-Brazil. Suitable gem material has been found in numerous parts of
-the United States. Paris and Hebron in Maine have produced gorgeous
-pink and green crystals, and Auburn in the same state has supplied
-deep-blue, green, and lilac stones. Fine crystals, mostly green, but
-also pink and particoloured, occur in an albite quarry near the Conn
-River at Haddam Neck, Connecticut. All former localities have, however,
-been surpassed by the extraordinary abundance of superb green, and
-especially pink, crystals at Pala and Mesa Grande in San Diego County,
-California. As elsewhere, many-hued stones are common. The latter
-locality supplies the more perfectly transparent crystals. Kunz states
-that two remarkable rubellite crystals were found there, one being 45
-mm. in length and 42 mm. in diameter, and the other 56 mm. in length
-and 24 mm. in diameter. Madagascar, which has proved of recent years
-to be rich in gem-stones, supplies green, yellow, and red stones, both
-uniformly tinted and particoloured, which in beauty, though perhaps not
-in size, bear comparison with any found elsewhere.
-
-
-
-
- CHAPTER XXV
-
- PERIDOT
-
-
-The beautiful bottle-green stone, which from its delicate tint has
-earned from appreciative admirers the poetical _sobriquet_ of the
-evening emerald, and which has during recent years crept into popular
-favour and now graces much of the more artistic jewellery, is named
-as a gem-stone peridot—a word long in use among French jewellers, the
-origin and meaning of which has been forgotten—but is known to science
-either as olivine, on account of the olive-green colour sometimes
-characterizing it, or as chrysolite. It is of interest to note that the
-last word, derived from χρυσός, golden, and λίθος, stone, was in use at
-the time of Pliny, but was employed for topaz and other yellow stones,
-while his topaz, curiously enough, designated the modern peridot (cf.
-p. 199), an inversion that has occurred in other words. The true
-olivine must not be confused with the jewellers’ ‘olivine,’ which is a
-green garnet from the Ural Mountains (p. 217). Peridot is comparatively
-soft, the hardness varying from 6½ to 7 on Mohs’s scale, and is
-suitable only for articles which are not likely to be scratched; the
-polish of a peridot worn in a ring would soon deteriorate. The choicest
-stones are in colour a lovely bottle-green (Plate XXIX, Fig. 2) of
-various depths; the olive-green stones (Plate XXIX, Fig. 3) cannot
-compare with their sisters in attractiveness. The step form of cutting
-is considered the best for peridot, but it is sometimes cut round or
-oval in shape, with brilliant-cut fronts.
-
-Peridot is a silicate of magnesium and iron, corresponding to the
-formula (Mg,Fe)_{2}SiO_{4}, ferrous iron, therefore, replacing
-magnesia. To the ferrous iron it is indebted for its colour, the
-pure magnesium silicate being almost colourless, and the olive tint
-arises from the oxidation of the iron. The latitude in the composition
-resulting from this replacement is evinced in the considerable range
-that has been observed in the physical characters, but the crystalline
-symmetry persists unaltered; the lower values correspond to the stones
-that are usually met with as gems. Peridot belongs to the orthorhombic
-system of crystalline symmetry, and the crystals, which display a
-large number of faces, are prismatic in form and generally somewhat
-flattened. The stones, however, that come into the market for cutting
-as gems are rarely unbroken. The dichroism is rather faint, one of the
-twin colours being slightly more yellowish than the other, but it is
-more pronounced in the olive-tinted stones. The values of the least
-and greatest of the principal indices of refraction vary greatly,
-from 1·650 and 1·683 to 1·668 and 1·701, but the double refraction,
-amounting to 0·033, remains unaffected. Peridot, though surpassed by
-sphene in extent of double refraction, easily excels all the ordinary
-gem-stones in this respect, and this character is readily recognizable
-in a cut stone by the apparent doubling of the opposite edges when
-viewed through the table facet (cf. p. 41). An equally large
-variation occurs in the specific gravity, namely, from 3·3 to 3·5.
-
-[Illustration: _PLATE XXVII_
-
- 1. RUBELLITE
- 2. TOURMALINE
- 3. BALAS-RUBY
- 4. BLUE SPINEL
- 5. QUARTZ
- 6. WHITE OPAL
- 7. AMETHYST
- 8. TOURMALINE
- 9. BLACK OPAL
- 10. FIRE OPAL
- 11. ALEXANDRITE (_By daylight_)
- 12. CHRYSOBERYL
- 13. ALEXANDRITE (_By artificial light_)
-
-GEM-STONES]
-
-Peridots of deep bottle-green hue command moderate prices at the
-present day, about 30s. a carat being asked for large stones; the paler
-tinted stones run down to a few shillings a carat. The rate per carat
-may be very much larger for stones of exceptional size and quality.
-
-Olivine, to use the ordinary mineralogical term, is a common and
-important constituent of certain kinds of igneous rocks, and it is
-also found in those strange bodies, meteorites, which come to us
-from outer cosmical space. Except in basaltic lavas, it occurs in
-grains and rarely in well-shaped crystals. Stones that are large and
-transparent enough for cutting purposes come almost entirely from the
-island Zebirget or St. John situated on the west coast of the Red Sea,
-opposite to the port of Berenice. This island belongs to the Khedive of
-Egypt, and is at present leased to a French syndicate. It is believed
-to be the same as the mysterious island which produced the ‘topaz’
-of Pliny’s time. Magnificent stones have been discovered here, rich
-green in colour, and 20 to 30, and occasionally as much as 80, carats
-in weight when cut; a rough mass attained to the large weight of 190
-carats. Pretty, light-green stones are supplied by Queensland, and
-peridots of a less pleasing dark-yellowish shade of green, and without
-any sign of crystal form, have during recent years come from North
-America. Stones rather similar to those from Queensland have latterly
-been found in the Bernardino Valley in Upper Burma, not far from the
-ruby mines.
-
-
-
-
- CHAPTER XXVI
-
- ZIRCON
-
- (_Jargoon_, _Hyacinth_, _Jacinth_)
-
-
-Zircon, which, if known at all in jewellery, is called by its variety
-names, jargoon and hyacinth or jacinth, is a species that deserves
-greater recognition than it receives. The colourless stones rival
-even diamond in splendour of brilliance and display of ‘fire’; the
-leaf-green stones (Plate XXIX, Fig. 13) possess a restful beauty
-that commends itself; the deep-red stones (Plate XXIX, Fig. 14), if
-somewhat sombre, have a certain grandeur; and no other species produces
-such magnificent stones of golden-yellow hue (Plate XXIX, Fig. 12).
-Zircon is well known in Ceylon, which supplies the world with the
-finest specimens, and is highly appreciated by the inhabitants of that
-sunny isle, but it scarcely finds a place in jewellery elsewhere. The
-colourless stones are cut as brilliants, but brilliant-cut fronts with
-step-cut backs is the usual style adopted for the coloured stones.
-
-Zircon is a silicate of zirconium corresponding to the formula
-ZrSiO_{4}, but uranium and the rare earths are generally present in
-small quantities. The aurora-red variety is known as hyacinth or
-jacinth, and the term jargoon is applied to the other transparent
-varieties, and especially to the yellow stones. The most attractive
-colours shown by zircon are leaf-green, golden-yellow, and deep red.
-Other common colours are brown, greenish, and sky-blue. Colourless
-stones are not found in nature, but result from the application of heat
-to the yellow and brown stones.
-
-The name of the species is ancient, and comes from the Arabic _zarqūn_,
-vermilion, or the Persian _zarqūn_, gold-coloured. From the same
-source in all probability is derived the word jargoon through the
-French _jargon_ and the Italian _giacone_. Hyacinth (cf. p. 211) is
-transliterated from the Greek ὑάκινθος, itself adapted from an old
-Indian word; it is in no way connected with the flower of the same
-name. The last word has seen some changes of meaning. In Pliny’s time
-yellow zircons were indiscriminately classified with other yellow
-stones as chrysolite. His hyacinth was used for the sapphire of the
-present day, but was subsequently applied to any transparent corundum.
-Upon the introduction of the terms, sapphire and ruby, for the blue and
-the red corundum hyacinth became restricted to the other varieties, of
-which the yellow was the commonest. In the darkness of the Middle Ages
-it was loosely employed for all yellow stones emanating from India,
-and was finally, with increasing discernment in the characters of
-gem-stones, assigned to the yellow zircon, since it was the commonest
-yellow stone from India.
-
-[Illustration: FIG. 78.—Zircon Crystal.]
-
-Considered from the scientific point of view, zircon is by far the most
-interesting and the most remarkable of the gem-stones. The problem
-presented by its characters and constitution is one that still awaits
-a satisfactory solution. Certain zircons, which are found as rolled
-pebbles in Ceylon and never show any trace of crystalline faces, have
-very nearly single refraction, and the values of the refractive index
-vary from 1·790 to 1·840, and the specific gravity is about 4·00 to
-4·14, and the hardness is slightly greater than that of quartz, being
-about 7¼. On the other hand, such stones as the red zircons from
-Expailly have remarkably different properties. They show crystalline
-faces with tetragonal symmetry, the faces present being four prismatic
-faces mutually intersecting at right angles and four inclined faces at
-each end (Fig. 78). They have large double refraction, varying from
-0·044 to 0·062, which is readily discerned in a cut stone (cf. p.
-41), and the refractive indices are high, the ordinary index varying
-from 1·923 to 1·931 and the extraordinary from 1·967 to 1·993. Since
-the ordinary is less than the extraordinary index the sign of the
-double refraction is positive. The specific gravity likewise is much
-higher, varying from 4·67 to 4·71. The second type, therefore, sinks
-in molten silver-thallium nitrate, whereas the first type floats. The
-second type is also slightly harder, being about 7½ on Mohs’s scale.
-By heating either of these types the physical characters are not much
-altered, except that the colour is weakened or entirely driven off and
-some change takes place in the double refraction. But between these
-two types may be found zircons upon which the effect of heating is
-striking. They seem to contract in size so that the specific gravity
-increases as much as three units in the first place of decimals, and a
-corresponding increase takes place in the refractive indices, and in
-the amount of double refraction. The cause of these changes remains a
-matter of speculation. Evidently a third type of zircon exists which
-is capable of most intimate association with either of the other
-types, and which is very susceptible to the effect of heat. It may be
-noted that stones of the intermediate type are usually characterized
-by a banded or zonal structure suggesting a want of homogeneity. The
-theory has been advanced that zircon contains an unknown element which
-has not yet been separated from zirconium. Zircon of the first type
-favours green, sky-blue, and golden-yellow colours; honey-yellow, light
-green, blue, and red colours characterize the second type; and the
-intermediate stones are mostly yellowish green, cloudy blue, and green.
-
-It is another peculiarity of zircon that it sometimes shows in the
-spectroscope absorption bands (p. 61), which were observed in 1866 by
-Church. Many zircons do not exhibit the bands at all, and others only
-display the two prominent bands in the red end of the spectrum.
-
-Of all the gem-stones zircon alone approaches diamond in brilliance of
-lustre, and it also possesses considerable ‘fire’; it can, of course,
-be readily distinguished by its inferior hardness, but a judgment based
-merely on inspection by eye might easily be erroneous.
-
-According to Church, who has made a lifelong study of zircon, the green
-and yellowish stones of the first variety emit a brilliant orange light
-when being ground on a copper wheel charged with diamond dust, and
-the golden stones of the intermediate type glow with a fine orange
-incandescence in the flame of a bunsen burner; the latter phenomenon is
-supposed to be due to the presence of thoria.
-
-The leaf-green stones almost invariably show a series of parallel bands
-in the interior.
-
-Zircons vary from 5s. to 15s. a carat, but exceptional stones may be
-worth more.
-
-By far the finest stones come from Ceylon. The colourless stones are
-there known as ‘Matura diamonds,’ and the hyacinth includes garnet
-(hessonite) of similar colour, which is found with it in the same
-gravels. The stones are always water-worn. Small hyacinths and deep-red
-stones come from Expailly, Auvergne, France, and yellowish-red crystals
-are found in the Ilmen Mountains, Orenburg, Russia. Remarkably fine
-red stones have been discovered at Mudgee, New South Wales, and
-yellowish-brown stones accompany diamond at the Kimberley mines, South
-Africa.
-
-
-
-
- CHAPTER XXVII
-
- CHRYSOBERYL
-
- (_Chrysolite_, _Cat’s-Eye_, _Cymophane_, _Alexandrite_)
-
-
-Chrysoberyl has at times enjoyed fleeting popularity on account of the
-excellent cat’s-eyes cut from the fibrous stones, and in the form of
-alexandrite it meets with a steadier, if still limited, demand. It is a
-gem-stone that is seldom met with in ordinary jewellery, although its
-considerable hardness befits it for all such purposes.
-
-Chrysoberyl is in composition an aluminate of beryllium corresponding
-to the formula BeAl_{2}O_{4}, and is therefore closely akin to spinel.
-It usually contains some ferric and chromic oxides in place of alumina,
-and ferrous oxide in place of beryllia, and it is to these accessory
-constituents that its tints are due. Other gem-stones containing the
-uncommon element beryllium are phenakite and beryl. Pale yellowish
-green, the commonest colour, is supposed to be caused by ferrous
-oxide; such stones are known to jewellers as chrysolite (Plate XXVII,
-Fig. 12). Cat’s-eyes (Plate XXIX, Fig. 1) have often also a brownish
-shade of green. The bluish green and dark olive-green stones known
-as alexandrite (Plate XXVII, Figs. 11, 13) differ in appearance so
-markedly from their fairer sisters that their common parentage seems
-almost incredible. The dull fires that glow within them, and the
-curious change that comes over them at night, add a touch of mystery to
-these dark stones. Chromic oxide is held responsible for their colour.
-The cat’s-eyes are, of course, always cut _en cabochon_, but otherwise
-chrysoberyl is faceted.
-
-The name of the species is composed of two Greek words, χρυσός, golden,
-and βήρυλλος, beryl, and etymologically more correctly defines the
-lighter-coloured stones, which were, indeed, at one time the only kind
-known. Chrysolite from χρυσὁς, golden, and λίθος, stone, has much the
-same significance. This name is preferred by jewellers, but in science
-it is applied to an entirely different species, which is known in
-jewellery as peridot. Cymophane, from κῦμα, wave, and φαίνειν, appear,
-refers to the peculiar opalescence characteristic of cat’s-eyes; it
-is sometimes used to designate these stones, but does not find a
-place within the vocabulary of jewellery. Alexandrite is named after
-Alexander II, Czar of Russia, because it first came to light on his
-birthday. That circumstance, coupled with its display of the national
-colours, green and red, and its at one time restriction to the mining
-district near Ekaterinburg, renders it dear to the heart of all loyal
-Russians.
-
-Chrysoberyl crystallizes in the orthorhombic system, and occurs in
-rather dull, complex crystals, which are sometimes so remarkably
-twinned, especially in the variety called alexandrite, as to simulate
-hexagonal crystals. In keeping with the crystalline symmetry it
-is doubly refractive and biaxial, having two directions of single
-refraction. The least and the greatest of the principal indices of
-refraction may have any values between 1·742 and 1·749, and 1·750 and
-1·757, respectively, the maximum amount of double refraction remaining
-always the same, namely, 0·009. The mean principal refractive index
-is close to the least; the sign of the double refraction is therefore
-positive, and the shadow-edge corresponding to the lower index, as
-seen in the refractometer, has little, if any, perceptible motion
-when the stone is rotated. The converse is the case with corundum;
-the sign is negative, and it is the shadow-edge corresponding to the
-greater refractive index that remains unaltered in position on rotation
-of the stone. This test would suffice to separate chrysoberyl from
-yellow corundum, even if the refractive indices of the former were
-not sensibly lower than those of the latter. Also, the dichroism of
-chrysolite is stronger than that of yellow sapphires. In alexandrite
-this phenomenon is most prominent; the absorptive tints, columbine-red,
-orange, and emerald-green, corresponding to the three principal
-optical directions, are in striking contrast, and the first differs
-so much from the intrinsic colour of the stone as to be obvious to
-the unaided eye, and is the cause of the red tints visible in a cut
-stone. The curious change in colour of alexandrite, from leaf-green to
-raspberry-red, that takes place when the stone is seen by artificial
-light, is due to a different cause, as has been pointed out above (p.
-54). The effect is illustrated by Figs. 11, 13 on Plate XXVII, which
-represent a fine Ceylon stone as seen by daylight and artificial light;
-the influence of dichroism may be noticed in the former picture. The
-specific gravity of chrysoberyl varies from 3·68 to 3·78. In hardness
-this species ranks above spinel and comes next to corundum, being
-given the symbol 8½ on Mohs’s scale. Certain stones contain a multitude
-of microscopic channels arranged in parallel position. When the stones
-are cut with their rounded surface parallel to the channels, a broadish
-band of light is visible running across the stone at right angles
-to them, and suggests the pupil of a cat’s eye, whence the common
-name for the stones. The fact that the channels are hollow causes an
-opalescence, which is absent from the quartz cat’s-eye.
-
-The most important locality for the yellowish chrysoberyl is the rich
-district of Minas Novas, Minas Geraes, Brazil, where it occurs in the
-form of pebbles, and excellent material is also supplied by Ceylon,
-in both crystals and rounded pebbles. Other places for chrysolite are
-Haddam, Connecticut, and Greenfield, Saratoga County, New York, in
-the United States, and recently in the gem-gravels near the Somabula
-Forest, Rhodesia. Ceylon supplies some of the best cat’s-eyes.
-Alexandrite was first discovered, as already stated, at the emerald
-mines near Ekaterinburg, in the Urals; but the supply is now nearly
-exhausted. A poorer quality comes from Takowaja, also in the Urals.
-Good alexandrite has come to light in Ceylon, and most of the stones
-that are placed on the market at the present day have emanated from
-that island. The Ceylon stones reach a considerable size, often as much
-as from 10 to 20 carats in weight; the Russian stones have a better
-colour and are more beautiful, but they are less transparent, and
-rarely exceed a carat in weight. Good chrysolite may be worth from 10s.
-to £2 a carat, and cat’s-eye runs from £1 to £4 a carat, depending
-upon the quality. Alexandrites meet with a steady demand in Russia, and
-fine stones are scarce; flawless stones about a carat in weight are
-worth as much as £30 a carat, and even quite ordinary stones fetch £4 a
-carat.
-
-From Ceylon, that interesting home of gems, have originated some
-magnificent chrysoberyls, including a superb chrysolite, 80¾ carats
-in weight, and another, a splendid brownish yellow in colour and
-very even in tint, and two large alexandrites, green in daylight and
-a rich red by night, weighing 63⅜ and 28-23/32 carats. The finest
-cut chrysolite existing is probably the one exhibited in the Mineral
-Gallery of the British Museum (Natural History). Absolutely flawless
-and weighing 43¾ carats, it was formerly contained in the famous Hope
-collection, and is described on page 56 and figured on Plate XXI of
-the catalogue prepared by B. Hertz, which was published in 1839; the
-weight there given includes the brilliants and the ring in which it
-was mounted. It is shown, about actual size, in Plate XXVII, Fig. 12.
-A magnificent cat’s-eye, 35·5 by 35 mm. in size, which also formed
-part of the Hope collection, was included in the crown jewels taken
-from the King of Kandy in 1815. The crystalline markings in the cut
-stone are so arranged that the lower half shows an altar overhung by a
-torch. The stone has been famous in Ceylon for many ages. It was set
-in gold with rubies cut _en cabochon_. Two fine Ceylon alexandrites of
-exceptional merit, weighing 42 and 26¾ carats, are also exhibited in
-the Mineral Gallery of the British Museum (Natural History). The former
-is illustrated in Plate XXVII, Figs. 11, 13, as seen in daylight and in
-artificial light.
-
-
-
-
- CHAPTER XXVIII
-
- QUARTZ
-
- (_Rock-Crystal_, _Amethyst_, _Citrine_, _Cairngorm_, _Cat’s-Eye_,
- _Tiger’s-Eye_)
-
-
-Although the commonest and, in its natural form, the most easily
-recognizable of mineral substances, quartz nevertheless holds a not
-inconspicuous position among gem-stones, because, as amethyst (Plate
-XXVII, Fig. 7), it provides stones of the finest violet colour;
-moreover, the yellow quartz (Plate XXVII, Fig. 5) so ably vies with the
-true topaz that it is universally known to jewellers by the name of the
-latter species, and is too often confounded with it, and the lustrous,
-limpid rock-crystal even aspires to the local title of ‘diamond.’
-For all purposes where a violet or yellow stone is required, quartz
-is admirably suited; it is hard and durable, and it has the merit,
-or possibly to some minds the drawback, of being moderate in price.
-Despite its comparative lack of ‘fire,’ rock-crystal might replace
-paste in rings and buckles with considerable advantage from the point
-of view of durability. The chatoyant quartz, especially in the form
-known as tiger’s-eye, will for beauty bear comparison with the true
-cat’s-eye, which is a variety of chrysoberyl. Except that cat’s-eye is
-cut _en cabochon_, quartz is step- or sometimes brilliant-cut.
-
-Ranking with corundum next to diamond as the simplest in composition
-of the gem-stones, quartz is the crystallized form of silica, oxide
-of silicon, corresponding to the formula SiO_{2}. When pure, it
-is entirely devoid of the faintest trace of colour and absolutely
-water-clear. Such stones are called rock-crystal, and it is easy to
-understand why in early days it was supposed to represent a form
-of petrified water. It is these brilliant, transparent stones that
-are, when small, known in many localities as ‘diamonds.’ Before
-the manufacture of glass was discovered and brought to perfection,
-rock-crystal was in considerable use for fashioning into cups, vases,
-and so forth. The beautiful tints characterizing quartz are due to the
-usual metallic oxides. To manganese is given the credit of the superb
-purple or violet colour of amethyst, which varies considerably in
-depth. Jewellers are inclined to distinguish the deep-coloured stones
-with the prefix ‘oriental,’ but the practice is to be deprecated, since
-it might lead to confusion with the true oriental amethyst, which is
-a purple sapphire, one of the rarest varieties of corundum. Quartz
-of a yellow hue is properly called citrine, but, as already stated,
-jewellers habitually prefer the name ‘topaz’ for it, and distinguish
-the true topaz by the prefix Brazilian—not a very happy term, since
-both the yellow topaz and the yellow quartz occur plentifully in
-Brazil. Sometimes the yellow quartz is termed occidental, Spanish,
-or false topaz. Stones with a brownish or smoky tinge of yellow are
-called cairngorm, or Scotch topaz. The colour of the yellow stones
-is doubtless due to a trace of ferric oxide. Stones of a smoky brown
-colour are known as smoky-quartz. Rose-quartz, which is rose-red or
-pink in colour and hazy in texture, is comparatively rare; strange
-to say, it has never been found in distinct crystals. The tint,
-which may be due to titanium, is fugitive, and fades on exposure to
-strong sunlight. In milky quartz, as the name suggests, the interior
-is so hazy as to impart to the stone a milky appearance. It has
-frequently happened that quartz has crystallized after the formation
-of other minerals, with the result that the latter are found inside
-it. Prase, or mother-of-emerald, which at one time was supposed to
-be the mother-rock of emerald, is a quartz coloured leek-green by
-actinolite fibres in the interior. Specimens containing hair-like
-fibres of rutile—the so-called _flêches d’amour_—are common in mineral
-collections, and are sometimes to be seen worked. When enclosing a
-massive, light-coloured, fibrous mineral, the stones have a chatoyant
-effect, and display, when suitably cut, a fine cat’s-eye effect; in
-tiger’s-eye the enclosed mineral is crocidolite, an asbestos, the
-original blue hue of which has been changed to a fine golden-brown
-by oxidation. Quartz which contains scales of mica, hematite, or
-other flaky mineral has a vivid spangled appearance, and is known
-as aventurine; it has occasionally been employed for brooches or
-similar articles of jewellery. Rainbow-quartz, or iris, is a quartz
-which contains cracks, the chromatic effect being the result of the
-interference of light reflected from them; it has been artificially
-produced by heating the stone and suddenly cooling it.
-
-The name of the species is an old German mining term of unknown
-meaning which has been in general use in all languages since the
-sixteenth century. Amethyst is derived from ἀμέθυστος, not drunken,
-possibly from a foolish notion that the wearer was exempt from the
-usual consequences of unrestrained libations. Pliny suggests as an
-alternative explanation that its colour approximates to, but does not
-quite reach, that of wine. Aventurine, from _aventura_, an accident,
-was first applied to glass spangled with copper, the effect being
-said to have been accidentally discovered owing to a number of copper
-filings falling into a pot of molten glass in a Venetian factory.
-
-[Illustration: FIG. 79.—Quartz Crystal.]
-
-Quartz belongs to the hexagonal system of crystalline symmetry,
-and crystallizes in the familiar six-sided prisms terminated by
-six inclined, often triangular, faces (Fig. 79); twins are common,
-though they are not always obvious from the outward development. In
-accordance with the symmetry the refraction is double, and there is one
-direction of single refraction, namely, that parallel to the edge of
-the prism. The ordinary refractive index has the value 1·544, and the
-extraordinary 1·553, and since the latter is the greater, the sign of
-the double refraction is positive. The double refraction is small in
-amount, but is large enough to enable the apparent doubling of certain
-of the opposite edges of a faceted stone to be perceptible when viewed
-with a lens through the table-facet. The dichroism of the deep-coloured
-stones is quite distinct. Quartz has only about the same amount of
-colour dispersion as ordinary glass, and lacks, therefore, ‘fire.’
-The application of strong heat tends, as usual, to weaken or drive
-off the colour. Thus the dense smoky-quartz found in Spain, Brazil,
-and elsewhere is converted into stones of a colour varying from light
-yellow to reddish brown according to the amount and duration of the
-application. In the case of amethyst the colour is changed to a deep
-orange, or entirely driven off if the temperature be high enough. Its
-density is very constant, varying only from 2·654 to 2·660; the purest
-stones are the lightest. To it has been assigned the symbol 7 on Mohs’s
-scale of hardness.
-
-To physicists quartz is one of the most interesting of minerals because
-of its power of rotating, to an extent depending upon the thickness of
-the section, the plane of polarization of a beam of light traversing it
-in a direction parallel to the prism edge. It appears, moreover, from
-a study of the pyro-electric and general physical characters, that its
-molecular structure has a helical arrangement, which, like all screws,
-may have a right- or left-handed character. Amethyst is, in fact,
-invariably composed of separate twin individuals, alternately right-
-and left-handed; in some remarkable crystals the section at right
-angles to the prism edge is composed of triangular sectors, alternately
-of different hands and of different tints—purple and white. To the
-twinning is due the rippled fracture and the feathery inclusions so
-characteristic of amethyst.
-
-Besides its use for ornamental purposes, quartz finds a place as the
-material for lenses intended for delicate photographic work, because
-its transparency to the ultra-violet light is so much greater than
-that of glass. Spectacle lenses made of it are in demand, because they
-are not liable to scratches, and retain, therefore, their polish
-indefinitely. When fused in the oxyhydrogen flame, quartz becomes a
-silica glass, of specific gravity 2·2 and hardness 5 on Mohs’s scale,
-which has proved of great service for laboratory ware, because it
-withstands sudden and unequal heating without any danger of fracture;
-it has also in fine threads been invaluable for delicate torsion work,
-because it acquires not the smallest amount of permanent twist, in this
-respect being superior to the finest silk threads.
-
-Clear rock-crystal fetches little more than the cost of the cutting;
-citrine and amethyst are worth from 1s. to 5s. a carat, depending
-upon the quality and size of the stone; smoky-quartz is practically
-valueless; rose-quartz realizes less than 1s. a carat; and the value
-of cat’s-eye is also small—only 1s. to 2s. 6d. a carat. Tiger’s-eye at
-one time commanded as much as 25s. a carat, but the supply exceeded the
-demand, with the consequent collapse in the price.
-
-Beautiful, brilliant, and limpid rock-crystal is found in various parts
-of the world: in the Swiss Alps, at Bourg d’Oisans in the Dauphiné
-Alps, France, in the famous Carrara marble, in the Marmaros Comitat
-of Hungary, and in the United States, Brazil, Madagascar, and Japan.
-Small lustrous stones, known in their localities as ‘Isle of Wight,’
-‘Cornish,’ or ‘Bristol diamonds,’ are found in our own country. Brazil
-supplies stones out of which have been cut the clear balls used in
-crystal-gazing. The finest amethysts come from Brazil—especially the
-State of Rio Grande do Sul—and from Uruguay, India, and the gem-gravels
-of Ceylon; good stones also occur at Ekaterinburg, in the Ural
-Mountains. A splendid Brazilian amethyst, weighing 334 carats, and
-two Russian stones—one hexagonal in contour, weighing 88 carats, and
-the other, a deep purple in colour with a circular table, weighing 73
-carats—are exhibited in the British Museum (Natural History). Cairngorm
-is known from the place of that name in Banffshire, Scotland, whence
-fine specimens have emanated; it is a gem much valued in that country.
-Fine cairngorm has also originated from Pike’s Peak, Colorado. Splendid
-yellow stones have had their birth in the States of Minas Geraes, São
-Paulo, and Goyãz, of Brazil—especially in the last. The fine Spanish
-smoky-quartz, which, as already stated, turns yellow on heating, comes
-from Hinojosa, in the Province of Cordova. The delicate rose-quartz
-is known at Bodenmais in Bavaria, Paris in Maine, United States, and
-Ekaterinburg in the Ural Mountains. The finest cat’s-eyes are found in
-India and Ceylon, and are high in favour with the natives. Greenish
-stones of an inferior quality are brought from the Fichtelgebirge in
-Bavaria, and are sold as ‘Hungarian cat’s-eyes,’ despite the fact
-that no such stone occurs in Hungary—another instance of jewellers’
-disdain for accuracy. Tiger’s-eye occurs in considerable quantity in
-the neighbourhood of Griquatown, Griqualand West, South Africa. A
-silicified crocidolite, in which the blue colour is retained, comes
-also from Salzburg, and is known as sapphire- or azure-quartz, or
-siderite.
-
-Certain of the pebbles found on the seashore of our coasts, especially
-off the Isle of Wight and North Wales, cut into attractive, clear
-stones, more or less yellow in colour; but examples suitable for the
-purpose are not so numerous as might be supposed, and do not reward any
-casual search. _Les affaires sont les affaires._ The local lapidary,
-instead of explaining that the pebbles brought to him are not worth
-cutting, finds it more convenient and profitable to substitute for
-them other, inferior and badly cut, stones, bought by the gross, or
-even paste stones; the customer, on the other hand, is contented with
-a pretty bauble, and is not grateful for the information that it might
-have been obtained for a fraction of the sum paid.
-
-
-
-
- CHAPTER XXIX
-
- CHALCEDONY, AGATE, ETC.
-
-
-Chalcedony and agate, and their endless varieties, are composed
-mainly of silica, but the separate individual crystals are so small
-as to be invisible to the unaided eyesight, and occasionally are
-so extremely minute that the structure is almost amorphous. The
-colour and appearance vary greatly, depending upon the impurities
-contained in the stone, and, since both have been made a criterion for
-differentiation of types, a host of names have come into use, none of
-which are susceptible of strict definition. On the whole, these stones
-may be divided into two groups: chalcedony, in which the structure is
-concretionary and the colour comparatively uniform, and agate, in which
-the arrangement takes the form of bands, varying greatly in tint and
-colour.
-
-The refraction, though double in the individual, is irregular over the
-stone as a whole, and the indices approximate to 1·550. The specific
-gravity ranges from 2·62 to 2·64, depending upon the impurities
-present. The degree of hardness is about the same as that of quartz,
-namely, 7 on Mohs’s scale. All kinds are more or less porous, and
-stones of a dull colour are therefore artificially tinted after being
-worked.
-
-The term chalcedony, derived from χαλκηδών the name of a town in
-Asia Minor, is usually confined to stones of a greyish tinge. Stones
-artificially coloured an emerald green have been cut and put upon
-the market as ‘emeraldine.’ Carnelian is a clear red chalcedony,
-and sard is somewhat similar, but brownish in tint. Chrysoprase is
-apple-green in colour, nickel oxide being supposed to be the agent.
-Prase (cf. p. 240), which is a dull leek-green in hue, may also in
-part be referred here; the name comes from πράσμον, a leek. Plasma,
-which may have the same derivation, is a brighter leek-green. Jasper
-is a chalcedony coloured blood-red by iron oxide, while bloodstone is
-a green chalcedony spotted with jasper; they are popular stones for
-signet rings. Flint, an opaque chalcedony, breaks with a sharp cutting
-edge, and was much in request with early man as a tool or a weapon; its
-property of giving sparks when struck with steel rendered it invaluable
-before the invention of matches. Hornstone is somewhat similar, but
-more brittle, while chert is a flinty rock.
-
-Agate, named after the river Achates in Sicily, where it was found at
-the time of Theophrastus, has a peculiar banded structure, the bands
-being usually irregular in shape, following the configuration of the
-cavity in which it was formed. Moss-agate, or mocha-stone, contains
-moss-like inclusions of some fibrous mineral. Onyx is an agate with
-regular bands, the layers having sharply different colours; when black
-and white, it has, in days gone by, been employed for cameos. Sardonyx
-is similar in structure, but red and white in colour. Agate is used in
-delicate balances for supporting the steel knife-edges of the balance
-itself and of the panholders, and is largely employed—especially when
-artificially coloured—for umbrella handles and similar articles.
-
-Chalcedony and agate are found the whole world over, but India, and
-particularly Brazil, are noted for their fine carnelians and agates.
-
-
-
-
- CHAPTER XXX
-
- OPAL
-
- (_White Opal_, _Black Opal_, _Fire-Opal_)
-
-
-That opal in early times excited keen admiration is evident from
-Pliny’s enthusiastic description of these stones: “For in them you
-shall see the burning fire of the carbuncle, the glorious purple of the
-amethyst, the green sea of the emerald, all glittering together in an
-incredible mixture of light.” During much of last century, owing to the
-foolish superstition that ill-luck dogs the footsteps of the wearer,
-the species lay under a cloud, which has even now not quite dispersed,
-but exercises a prejudicial effect upon the fortunes of the stone. It
-has, however, recently attracted considerable attention owing to the
-discovery of the splendid black opals in Australia; at one moment black
-with the darkness of night, at the next by a chance movement glowing
-with vivid crimson flame, such stones may justly be considered the most
-remarkable in modern jewellery. At the present day opal is divided by
-jewellers roughly into two main groups: ‘white’ (Plate XXVII, Fig. 6)
-and ‘black’ (Plate XXVII, Fig. 9), according as the tint is light or
-dark, fire-opal (Plate XXVII, Fig. 10) standing in a separate category.
-
-Opal differs from the rest of the principal gem-stones in being
-not a crystalline body, but a solidified jelly, and it depends for
-its attractiveness upon the characteristic play of colour, known,
-in consequence, as opalescence (cf. p. 39), which arises from a
-peculiarity in the structure. Opal is mainly silica, SiO_{2}, in
-composition, but contains in addition an amount of water varying in
-precious opal from 6 to 10 per cent. As the original jelly cooled, it
-became riddled throughout with cracks, which were afterwards generally
-filled with opal matter, containing a different amount of water,
-and therefore differing slightly in refractivity from the original
-substance. The structure not being quite homogeneous, each crack has
-the same action upon light as a soap-film, and gives rise to precisely
-similar phenomena; the thinner and more uniform the cracks, the greater
-the splendour of the chromatic display, the particular tint depending
-upon the direction in which the stone is viewed. The cracks in certain
-opals were not filled up, and therefore contain air. Such stones appear
-opaque and devoid of opalescence until plunged into water; they are
-consequently known as hydrophane, from ὕδωρ, water, and φαίνεσθαι, to
-make appear. Owing to the effect of total-reflection, light was stopped
-on the hither side of the cracks before they were filled with water,
-which is not far inferior to opal in refractivity; it is surprising how
-much water these stones will absorb.
-
-Opal is colourless when pure, but is nearly always more or less milky
-and opaque, or tinted various dull shades by ferric oxide, magnesia
-or, alumina. The so-called black opal is generally a dark grey or
-blue, and very rarely quite black. That the coloration is not due
-to ordinary absorption, but to the action of cracks in the stone,
-is shown by the fact that the transmitted light is complementary to
-the reflected light; the blue opal is, for instance, a yellow when
-held up so that light has passed through it. In many black opals the
-opalescent material occurs in far too tiny pieces to be cut separately,
-and the whole iron-stained matrix is cut and polished and sold under
-the name ‘opal-matrix.’ The reddish and orange-coloured stones known
-as fire-opal have pronounced colour and only slight milkiness; they
-display the customary opalescence in certain directions. These stones
-are often faceted, but otherwise opals are cut _en cabochon_, either
-flat or steep—generally the former in brooches and pendants, and the
-latter in rings. Opal is somewhat soft, varying from 5 to 6½ on Mohs’s
-scale, and is therefore easily scratched. The specific gravity ranges
-from 2·10 to 2·20, and the refractive index from 1·444 to 1·464, the
-refraction, of course, being always single. It is unwise to immerse
-opals in liquids on account of their porosity.
-
-The name opal comes to us through the Latin _opallus_, which was used
-for the same species as understood by the term at the present day, but
-the word has a far older origin, which has not been traced. The Romans
-also called the mineral _pæderos_, the Greek form of Cupid, a name
-applied to all rosy stones. The name cacholong, for the bluish-white
-porcelain variety, which is very porous and adheres to the tongue, is
-of Tartar origin; the stone is highly valued in the East.
-
-The oldest mines, which up to quite a recent date were the only
-extensive deposit of opal known, were at Cserwenitsa, near Kashau,
-in Hungary. From them in all probability emanated the opals known to
-the Romans. The opals from this locality were generally quite small,
-and large pieces were rare and commanded high prices. The Hungary
-mines, however, proved quite unable to compete with the rich fields
-at White Cliffs, New South Wales, in spite of the efforts that were
-made to depreciate and exclude from the market the new stones, and at
-the present time few of the opals on the market come from them. As so
-often happens, the White Cliffs deposit was discovered by accident.
-In 1889 a hunter, when tracking a wounded kangaroo, chanced to pick
-up an attractively coloured opal. The district is so waterless and
-forbidding that, but for such a chance, the opals might have long lain
-hidden. They occur in seams in deposits of Cretaceous Age in a variety
-of ways, filling cavities in rocks or sandstones, or cracks in wood, or
-replacing wood, saurian bones, and some spiky mineral, which may have
-been glauberite. In recent years, another rich deposit was discovered
-farther north, on both sides of the boundary between Queensland and
-New South Wales. The field is remarkable for the darkness of its
-opals, which are called ‘black opal’ in contradistinction to the
-lighter-coloured stones previously known. From Lightning Ridge in
-New South Wales come stones stained deep black which quite merit the
-designation black opal. The sandstone in which they are found is
-rich in iron, and this is no doubt responsible for the deepness of
-their tint. Mexico is noted for the fire-opal, which is found at
-Esperanza, Queretaro, and Zimapan; but other kinds of opal also are
-found at these places.
-
-[Illustration: _PLATE XXVIII_
-
-OPAL MINES, WHITE CLIFFS, NEW SOUTH WALES]
-
-The price of opal varies greatly, according to the intrinsic colour
-and the uniformity and brilliance of the opalescence. Common opal can
-be bought at as low a rate as 1s. a carat, while black opal ranges
-from 10s. to £8 a carat; but a good dark stone displaying a flaming
-opalescence commands a fancy figure, fine stones of this class being
-exceedingly rare. Fire-opal enjoys only a limited popularity now,
-though a few years ago it was in some demand; the price runs from 2s.
-to 10s. a carat.
-
-
-
-
- CHAPTER XXXI
-
- FELSPAR
-
- (_Moonstone, Sunstone, Labradorite, Amazon-Stone_)
-
-
-Though second to none among minerals in scientific interest, whether
-regarded from the point of view of their crystalline characters or
-the important part they play in the formation of rocks, the group
-included under the general name felspar occupies but a humble place
-in jewellery. It consists of three distinct species, orthoclase,
-albite, and anorthite, which are silicates of aluminium, and potassium,
-sodium, or calcium, corresponding to the formulae KAlSi_{3}O_{8},
-NaAlSi_{3}O_{8}, and CaAl_{2}Si_{2}O_{8} respectively, and also of
-species intermediate in composition between albite and orthoclase, or
-albite and anorthite. While differing in crystalline symmetry, all
-are characterized by two directions of cleavage which are nearly at
-right angles to one another. The double refraction, which is slight in
-amount, is biaxial in character and variable in sign. The values of the
-least and greatest of the indices of refraction range between 1·52 and
-1·53, and 1·53 and 1·55 respectively, the double refraction at the same
-time varying from 0·007 to 0·012. The specific gravity lies between
-2·48 and 2·66, and the hardness ranges between the degrees 6 and 7 on
-Mohs’s scale.
-
-Moonstone (Plate XXIX, Fig. 4), which is mainly pure orthoclase, alone
-is at all common in jewellery. It forms such an admirable contrasting
-frame for large coloured stones that it deserves greater popularity;
-no doubt the cheapness of the stones militates against their proper
-appreciation. The milky, bluish opalescence from which they take their
-name is caused by the reflection of light at the thin twin-lamellæ
-of which the structure is composed. They are always cut more or less
-steeply _en cabochon_. The finest stones were at one time cut from
-the felspar that came from the St. Gothard district in Switzerland
-and was in consequence known as adularia from the neighbouring Adular
-Mountains, somewhat incorrectly, since none occurs at the latter
-locality. At the present day practically all the moonstones on the
-market come from Ceylon. They run in price from £3 to £20 per oz. (28
-grams).
-
-Sunstone is a felspar containing flakes of hematite or goethite which
-impart a spangled bronze appearance to the stones. Good material occurs
-in parts of Norway. The remarkable sheen of labradorite or blue felspar
-has its origin in the interference of light at lamellar surfaces in
-the interior; the uniformity of the colour over comparatively large
-areas testifies to the regularity of the lamellar arrangement. The
-finest specimens were brought from the Isle of St. Paul off the coast
-of Labrador, where they were first discovered in 1770; large masses
-also occur on the coast itself. Amazon-stone is an opaque green felspar
-which occurs in the Ilmen Mountains, Orenburg, Russia, and at Pike’s
-Peak, Colorado, United States. It obtains its name from the Amazon
-River, where, however, none has ever been found; there may have been
-some confusion with a jade or similar stone.
-
-Occasionally clear colourless felspar has been faceted, and then
-closely resembles rock-crystal. A careful determination of the
-refractive indices and the specific gravity serves to discriminate
-between them.
-
-[Illustration: _PLATE XXIX_
-
- 1. CAT’S EYE
- 2. PERIDOT
- 3. PERIDOT
- 4. MOONSTONE
- 5. HESSONITE
- 6. PYROPE
- 7. DEMANTOID
- 8. ALMANDINE
- 9. SPODUMENE
- 10. KUNZITE
- 11. HIDDENITE
- 12. ZIRCON
- 13. ZIRCON
- 14. ZIRCON
- 15. ANDALUSITE
- 16. NEPHRITE
- 17. TURQUOISE
- 18. JADEITE
-
-GEM-STONES]
-
-
-
-
- CHAPTER XXXII
-
- TURQUOISE, ODONTOLITE, VARISCITE
-
-
-Of all the opaque stones turquoise (Plate XXIX, Fig. 17) alone finds a
-prominent place in jewellery and can aspire to rank with the precious
-stones. The colour varies from a sky-blue or a greenish blue to a
-yellowish green or apple-green. Only the former tints, which are at
-the same time the rarer, are in general demand, and they possess the
-great advantage of harmonizing with the tint of the gold setting.
-The blue colours are, especially in the case of the Siberian stones,
-by no means permanent, and fade in course of time. Turquoise is
-amorphous and seldom crystalline, and is therefore somewhat porous; it
-should consequently never be immersed in liquids or be contaminated
-with greasy and dirty matter lest the dreaded change of colour be
-brought about. The stones are translucent in thin sections, and a
-good observation is possible with the refractometer if the back of
-the stone is flat and polished, since only the section immediately
-adjacent to the instrument is concerned; the refractive index is about
-1·61. The specific gravity varies from 2·75 to 2·89. Turquoise has a
-hardness of slightly under 6 on Mohs’s scale, and takes a good polish,
-which is fairly durable, since on account of the comparative opacity
-of the stones scratches on the surface are not very noticeable.
-In composition it is a complex phosphate of aluminium and copper,
-corresponding to the formula CuOH.[6Al(OH)_{2}].H{5}.(PO_{4})_{4},
-with ferric oxide replacing some alumina. The blue colour is due to
-the copper constituent, and the predominance of iron may cause the
-greenish shades; but the water contained in the stones plays no mean
-part, since they turn a dirty green when it is driven off. The faded
-colour can sometimes be restored by immersion of the stone in ammonia
-and subsequent application of grease, but the effect is not lasting.
-Attempts are sometimes made to improve inferior stones by impregnating
-them with Berlin blue, but with only qualified success. Turquoises are
-said to be affected by the perspiration from the skin.
-
-The name of the species comes from a French word meaning Turkish, and
-arises from the fact that the gem-stone first reached Europe by way of
-Turkey. Another, but less obvious, suggestion is that it is derived
-from the Persian name for the species, _piruzeh_. Our turquoise and
-other phosphates of similar appearance were probably known to Pliny
-under the three names _callais_, _callaina_, and _callaica_.
-
-The finest turquoise still comes from the famous mines near Nishapur in
-the Persian province of Khorassan, where it was known in very ancient
-times; it is found with limonite filling the cracks and cavities
-in a brecciated porphyritic trachyte. Pieces of the turquoise and
-limonite from here are sometimes cut without removal of the latter,
-and sold as ‘turquoise-matrix,’ when the precious stones are too tiny
-to be worth separate working. It also occurs at Serbâl in the Sinai
-Peninsula. Among the more recent localities may be mentioned Los
-Cerillos Mountains, New Mexico; Sierra Nevada, Nevada, where pale blue
-and green stones are found; San Bernardino County, California, where
-again the stones are rather pale; and Arizona, where it occurs in pale
-greenish-blue stones.
-
-Some of the stones that have been seen are not the true turquoise but
-odontolite, or bone turquoise, which consists of the teeth and bones
-of mastodon or other extinct animals, phosphate of iron being the
-colouring material. These stones may easily be recognized by their
-organic structure, which is clearly visible if viewed with a strong
-lens or under the microscope. Moreover, odontolite invariably contains
-some calcium carbonate, and effervescence takes place if it be touched
-with hydrochloric acid. Turquoise dissolves in hydrochloric acid, but
-without effervescence, and since it contains copper, a fine blue colour
-is imparted to the solution by the addition of ammonia. Odontolite has
-a higher specific gravity, 3·0 to 3·5, but lower hardness, 5 on Mohs’s
-scale.
-
-Variscite, the hydrated phosphate of aluminium, corresponding to the
-formula AlPO_{4} + 2H_{2}O, is found in masses resembling a greenish
-turquoise, but it is much softer, being only 4 on Mohs’s scale. The
-specific gravity is 2·55. Round nodular masses of variscite are found
-in Utah.
-
-
-
-
- CHAPTER XXXIII
-
- JADE
-
-
-Though not usually accounted precious among European nations or in
-Western civilization in general, jade was held in extraordinary
-esteem by primitive man, and was fashioned by him into ornaments and
-utensils, often of considerable beauty, and even at the present day
-it ranks among the Chinese and Japanese peoples above all precious
-stones; indeed, the Chinese word _Yu_ and the Japanese words _Giyuku_
-or _Tama_ signify both jade and precious stones in general. According
-to the Chinese, jade is the prototype of all gems, and unites in
-itself the five cardinal virtues—_Jin_, charity; _Gi_, modesty; _Yu_,
-courage; _Ketsu_, justice; and _Chi_, wisdom. When powdered and mixed
-with water, it is supposed to be a powerful remedy for all kinds of
-internal disorders, to strengthen the frame and prevent fatigue, to
-prolong life, and, if taken in sufficient quantity just before death,
-to prevent decomposition.
-
-Jade is a general term that includes properly two distinct mineral
-species, nephrite or greenstone, and jadeite, which are very similar
-in appearance, both being fibrous and tough in texture, and more or
-less greenish in colour; but it is also applied to other species such
-as saussurite, californite, bowenite, and plasma, which have somewhat
-similar characters. The word jade is a corruption of the Spanish
-_pietra di hijada_, kidney-stone, in allusion to its supposed efficacy
-in diseases of that organ.
-
-Nephrite or greenstone (Plate XXIX, Fig. 16) is the commoner of
-the two jades. It is closely allied to the mineral hornblende, a
-silicate of magnesium, iron, and calcium corresponding to the formula
-Ca(Mg,Fe)_{3}(SiO_{3})_{4}, the magnesia being replaceable by ferrous
-oxide. Microscopic examination shows that the structure consists of
-innumerable independent fibres foliated or matted together, the former
-character giving rise to a slaty and the latter to a horny appearance
-in the stone as seen by the unaided eye. The colour varies from grey
-to leaf- and dark-green, the tint deepening as the relative amount of
-iron in the composition increases, and brown tints result from the
-oxidation of the iron along cracks in the stone. The hardness is 6½ on
-Mohs’s scale; nephrite is therefore about as hard as ordinary glass and
-softer than quartz. When polished, it always acquires a greasy lustre.
-The specific gravity ranges from 2·9 to 3·1. The least and greatest of
-the principal refractive indices are 1·606 and 1·632 respectively, the
-double refraction being biaxial and negative; the coloured fibres also
-display dichroism. All these differential effects are, however, masked
-in the stone because of the irregularity of the aggregation. Nephrite
-is fusible before the blowpipe, but only with difficulty. Its name is
-derived from the Greek word νεφρός, kidney, the allusion being the same
-as for jade.
-
-Many of the prehistoric implements found in Mexico and in the Swiss
-Lake Habitations are composed of nephrite, but it is uncertain where
-the mineral was obtained. Much of the material used by the Chinese
-at the present time comes from spots near the southern boundary of
-Eastern Turkestan, especially in the valleys of the rivers Karakash and
-Yarkand in the Kwen Lun range of mountains; it is also found farther
-north at the river Kashgar. It occurs in various provinces of China,
-namely, Shensi, Kwei Chau, Kwang Tung, Yunnan, and Manchuria. Gigantic
-waterworn boulders have been found in the Government of Irkutsk, near
-Lake Baikal, in eastern Siberia, the first discovery being made in the
-bed of the Onot stream by the explorer and prospector J. P. Alibert,
-in 1850. A large boulder of this kind, weighing over half a ton (1156
-lb., or 524·5 kg.), is exhibited in the Mineral Gallery of the British
-Museum (Natural History). An enormous mass, weighing over 2 tons (4718
-lb., or 2140 kg.), was discovered at Jordansmühl, Silesia, by Dr.
-G. F. Kunz, and is now in the magnificent collection of jade formed
-by Mr. Heber R. Bishop. Beautiful greenstone occurs in New Zealand,
-particularly in the Middle Island. The Maoris have long used it for
-various useful and ornamental purposes, the most common being indicated
-by their general name for the species, _punamu_, axe-stone; _kawakawa_
-is the ordinary green variety, a fine section of which is shown on the
-wall of the Mineral Gallery of the British Museum (Natural History),
-while _inanga_, a grey variety, and _kahurangi_, a pale-green and
-translucent variety, are rare and highly prized.
-
-Jadeite (Plate XXIX, Fig. 18) is by far the rarer of the two jades,
-and is the choicest gem with the Chinese. In composition it is a
-silicate of sodium and aluminium with the formula NaAl(SiO_{3})_{2},
-corresponding to the lithium mineral spodumene (p. 265). It has the
-same toughness and greasy lustre as nephrite, but is harder, being
-represented by the symbol 7 on Mohs’s scale, and thus only slightly,
-if at all, softer than quartz. The other characters are also higher;
-the specific gravity is about 3·34, and the least and greatest of the
-principal refractive indices are 1·66 and 1·68, the double refraction
-being biaxial and negative. The colour varies from white to almost
-an emerald green, the latter being especially prized, and often the
-green colour runs in streaks through the white. Jadeite fuses readily
-before the blowpipe to blebby glass, more easily than is the case with
-nephrite.
-
-The finest jadeite comes from the Mogaung district in Upper Burma,
-where it is found in boulders and also with albite in dykes in a
-dark-green serpentine. The export trade to China, which absorbs
-practically the whole of the output, is exceedingly valuable, and
-realizes nearly as much as the produce of the ruby mines. Jadeite is
-also found in the Shensi and Yunnan provinces of China, and in Tibet.
-
- • • • • •
-
-A few words may be said about the other jade-like minerals. Saussurite,
-which is named after H. B. de Saussure, has resulted from the
-decomposition of a felspar, and is nearly akin to the mineral zoisite.
-It has the customary toughness of structure, and is greenish grey to
-white in colour. Its specific gravity is about 3·2, and hardness 6½ to
-7 on Mohs’s scale. It occurs near Lake Geneva. Bowenite is a green
-serpentine (p. 289) which is found at Smithfield, Rhode Island, U.S.A.,
-and in New Zealand and Afghanistan. Californite and plasma are compact
-varieties of idocrase (p. 275) and chalcedony (p. 247) respectively.
-Verdite is a stone of rich green colour which is found in the form of
-large boulders in the North Kaap River, South Africa; it is composed of
-green mica (fuchsite) and some clayey matter.
-
-Jade has of recent years been imitated in glass, but the latter is
-recognizable by its vitreous lustre and inferior hardness, and sooner
-or later by its frangibility.
-
-
-
-
- CHAPTER XXXIV
-
- SPODUMENE, IOLITE, BENITOITE
-
-
- SPODUMENE
-
- (_Kunzite_, _Hiddenite_)
-
-Till a few years ago scarcely known outside the ranks of mineralogists,
-spodumene suddenly leaped into notice in 1903 upon the discovery of the
-lovely lilac-coloured stones (Plate XXIX, Fig. 10) at Pala, San Diego
-County, California; they shortly afterwards received the name kunzite
-after the well-known expert in gems, Dr. G. F. Kunz. The stones were
-found here in a pegmatite dyke, and were of all shades, ranging from
-pale pink to deep lilac, and at times as much as 150 carats in weight.
-Paler kunzite occurs with beryl and tourmaline at Coahuila Mountain
-in Riverside County, California, and colourless stones have recently
-come to light in Madagascar. Kunzite is remarkable for its wonderful
-dichroism; the beautiful violet tint that springs out in one direction
-comes with greater surprise because of the uninteresting yellowish
-tints in other directions. Unlike spodumene in general, kunzite is
-phosphorescent under the influence of radium.
-
-The emerald-green variety (Plate XXIX, Fig. 11), named hiddenite after
-Mr. W. E. Hidden, who discovered in 1881 the only known occurrence, in
-Alexander County, North Carolina, would no doubt have become popular
-had the supply of material not been so very limited; few stones were
-found, and the variety has never come to light elsewhere. The colour is
-supposed to be due to chromic acid. Hiddenite being also dichroic, the
-tint varies with the direction.
-
-Spodumene is ordinarily rather a pale yellowish in hue, and, as its
-name (which is derived from σποδίος, ash-coloured) suggests, is not
-very attractive. Clear, lemon-yellow stones (Plate XXIX, Fig. 9) are
-found in Brazil and Madagascar.
-
-The species is interesting scientifically because it contains the
-rare element lithium; it is a silicate of aluminium and lithium,
-corresponding to the formula LiAl(SiO_{3})_{2}. The double refraction
-is biaxial in character and positive in sign, the least and greatest
-of the refractive indices being 1·660 and 1·675; the specific gravity
-is 3·185, and hardness 6½ to 7 on Mohs’s scale. Spodumene has an easy
-cleavage, and the cut stones call therefore for careful handling, lest
-they be flawed or fractured. Two faceted stones, a beautiful kunzite
-and a fine hiddenite, weighing 60 and 2½ carats respectively, are
-exhibited in the British Museum (Natural History).
-
-
- IOLITE
-
-Known also by various other names—cordierite, dichroite, and
-water-sapphire (_saphire d’eau_)—this species owes its interest
-to the remarkable dichroism characterizing it, the principal
-colours—smoky-blue and yellowish white—being in such contrast as to
-be obvious to the unaided eye. The stones that are usually worked have
-intrinsically a smoky-blue colour, and are found in waterworn masses
-in the river-gravels of Ceylon, whence is the origin of the name
-water-sapphire. Iolite, from ἴον, violet, and λίθος, stone, refers to
-the colour; cordierite is named after Cordier, a French geologist, who
-first studied the crystallography of the species; and dichroite, of
-course, alludes to the most prominent character of the species.
-
-Iolite is a silicate of aluminium and of magnesium and iron
-corresponding to the formula H_{2}(Mg,Fe)_{4}Al_{8}Si_{10}O_{37}.
-The double refraction is small in amount, biaxial in character, and
-negative in sign, the least and greatest of the refractive indices
-being 1·543 and 1·551; the specific gravity is 2·63, and hardness 7 on
-Mohs’s scale. Iolite, if used, is worked and polished; it is seldom
-faceted. A large worked piece, weighing 177 grams, which was formerly
-in the Hawkins Collection, is exhibited in the British Museum (Natural
-History).
-
-
- BENITOITE
-
-The babe among gem-stones, benitoite first saw the light of day a few
-years ago, early in 1907. It occurs with the rare mineral neptunite,
-which was previously known only from Greenland, in narrow veins of
-natrolite in Diablo Range near the head-waters of the San Benito River,
-San Benito County, California. Despite careful search the species has
-not been found except within the original restricted area. To science
-it is interesting both because of its composition, a silico-titanate
-of barium, corresponding to the formula BaTiSi_{3}O_{9}, and because
-its crystals belong to a class of crystalline symmetry which has
-hitherto not been represented among minerals. The double refraction
-is uniaxial, and since the ordinary index of refraction is 1·757 and
-the extraordinary 1·804, it is positive in sign and large in amount,
-namely, 0·047. The stones are characterized by strong dichroism, the
-colour corresponding to the ordinary ray being white, and to the
-extraordinary greenish blue to indigo depending upon the tint of the
-stone. To obtain the best effect the stone must therefore be cut with
-the table-facet parallel to the crystallographic axis. The specific
-gravity is 3·65, and hardness 6½ on Mohs’s scale. When first discovered
-the species was supposed to be sapphire, and many stones were cut and
-sold as such. It is, however, much softer than sapphire, and is readily
-distinguished by its optical characters, since it possesses greater
-double refraction and of differing sign, so that, when tested with the
-refractometer, the shadow-edge corresponding to the lower index of
-refraction remains fixed in the case of benitoite, whereas the contrary
-happens with sapphire. Benitoite also, unlike sapphire, fuses easily
-to a transparent glass. Its blue colour, which is supposed to be due
-to a small amount of free titanic acid present, appears to be stable.
-Several stones as large as 1½ to 2 carats in weight have been found.
-The largest of all, perfectly flawless, weighs just over 7 carats, and
-is remarkable because it is about three times the next largest in point
-of weight; it is the property of Mr. G. Eacret, of San Francisco.
-
-
-
-
- CHAPTER XXXV
-
- EUCLASE, PHENAKITE, BERYLLONITE
-
-
- EUCLASE
-
-This species comes near beryl in chemical composition, being a
-silicate of aluminium and beryllium corresponding to the formula
-Be(AlOH)SiO_{4}, and closely resembles aquamarine in colour and
-appearance when cut. Owing to the rarity of the mineral good specimens
-command high prices for museum collections, and it is seldom worth
-while cutting it for jewellery. It derives its name from its easy
-cleavage, εὖ easily, and κλάσις fracture. The double refraction is
-biaxial in character and positive in sign, the least and greatest of
-the refractive indices being 1·651 and 1·670 respectively; the specific
-gravity is 3·07, and the hardness 7½ on Mohs’s scale. The colour is
-usually a sea-green, but sometimes blue. Euclase occurs with topaz at
-the rich mineral district of Minas Novas, Minas Geraes, Brazil, and has
-also been found in the Ural district, Russia.
-
-
- PHENAKITE
-
-Another beryllium mineral, phenakite owes its name to the frequency
-with which it has been mistaken for quartz, being derived from φέναξ,
-deceiver. The clear, colourless crystals, somewhat complex in form,
-have at times been cut, but they lack ‘fire,’ and despite their
-brilliant lustre meet with little demand. The composition is a silicate
-of beryllium corresponding to the formula Be_{2}SiO_{4}. The double
-refraction is uniaxial, and since the ordinary, 1·652, is less than
-the extraordinary index, 1·667, it is positive in sign; the specific
-gravity is 2·99, and the hardness is almost equal to that of topaz,
-being about 7½ to 8 on Mohs’s scale.
-
-Fine stones have long been known near Ekaterinburg in the Ural
-Mountains, and have recently been discovered in Brazil.
-
-
- BERYLLONITE
-
-As its name suggests, this mineral also contains beryllium, being
-a soda phosphate corresponding to the formula NaBePO_{4}. Clear,
-colourless stones, which occur at Stoneham, Maine, U.S.A., have been
-cut, but the lack of ‘fire,’ the easy cleavage, and comparative
-softness, the symbol being 5½ on Mohs’s scale, unfit it for use in
-jewellery. The double refraction is biaxial in character and negative
-in sign, the least and the greatest of the refractive indices being
-1·553 and 1·565 respectively.
-
-
-
-
- CHAPTER XXXVI
-
- ENSTATITE, DIOPSIDE, KYANITE, ANDALUSITE, IDOCRASE, EPIDOTE,
- SPHENE, AXINITE, PREHNITE, APATITE, DIOPTASE
-
-
- ENSTATITE
-
- (‘_Green Garnet_’)
-
-The small green stones which accompany the diamond in South Africa have
-been cut and put on the market as ‘green garnet.’ They are, however,
-in no way connected with garnet, but belong to a mineral species
-called enstatite, which is a silicate of magnesium corresponding to
-the formula MgSiO_{3}; the green colour is due to a small amount of
-ferrous oxide which replaces magnesia. The double refraction is biaxial
-in character and positive in sign, the least and greatest of the
-refractive indices being 1·665 and 1·674 respectively; the specific
-gravity ranges from 3·10 to 3·13, and the hardness is only about 5½
-on Mohs’s scale. The dichroism is perceptible, the twin-colours being
-yellowish and green, and, as usual, is more pronounced the deeper the
-colour of the stone. There is also a good cleavage in two different
-directions.
-
-With increasing percentage amount of iron enstatite passes into
-hypersthene. The colour becomes a dark brownish green, and an increase
-takes place in the physical constants, the least and greatest of the
-refractive indices attaining to 1·692 and 1·705 respectively, and
-the specific gravity ranging from 3·4 to 3·5. Hypersthene is never
-sufficiently transparent for faceting, but when spangled with small
-scales of brookite it is sometimes cut _en cabochon_.
-
-The name enstatite is derived from ἐνστάτης, an opponent, referring to
-the infusibility of the mineral before the blowpipe, and hypersthene
-comes from ὑπερσθένος, very tough.
-
-An altered enstatite, leek-green in colour and with nearly the
-composition of serpentine (p. 289), has been cut _en cabochon_. It has
-much lower specific gravity, only 2·6, and lower hardness, 3½ to 4 on
-Mohs’s scale. It is named bastite from Baste in the Harz Mountains,
-where it was first discovered.
-
-
- DIOPSIDE
-
-This species, which is also known as malacolite and alalite, provides
-stones of a leaf-green colour which have occasionally been cut. It
-is a silicate of calcium and magnesium corresponding to the formula
-MgCa(SiO_{3})_{2}, but usually contains in place of magnesia some
-ferrous oxide, to which it owes its colour; with increase in the
-percentage amount of iron the colour deepens and the physical constants
-change. The double refraction is large in amount, 0·028, biaxial
-in character, and positive in sign. The least and greatest of the
-refractive indices corresponding to the stones suitable for jewellery
-range about 1·671 and 1·699 respectively, but they may be as high as
-1·732 and 1·750 in the two cases. The specific gravity varies from 3·20
-to 3·38, and the hardness from 5 to 6 on Mohs’s scale. Dichroism is
-noticeable in deep-coloured stones, but is not very marked.
-
-The name diopside comes from δίς, double, and ὄψις, appearance, in
-allusion to the effect resulting from the double refraction; malacolite
-is derived from μαλακός, soft, because the mineral is softer than the
-felspar associated with it; and alalite is named after the principal
-locality, Ala Valley, Piedmont, Italy.
-
-
- KYANITE
-
-Kyanite, also known as disthene, is interesting for two reasons. Its
-structure is so grained in character that the hardness varies in the
-same stone from 5 to 7 on Mohs’s scale; it can therefore be scratched
-by a knife in some directions, but not in others (p. 79). It has the
-same chemical composition as andalusite, both being silicates of
-aluminium corresponding to the formula Al_{2}SiO_{5}, but possesses
-very different physical characters, a fact which shows how large
-a share the molecular grouping has in determining the aspect of
-crystallized substances. It is biaxial with small negative double
-refraction, the least and greatest of the refractive indices being
-1·72 and 1·73 respectively; the specific gravity is 3·61. It occurs in
-sky-blue prismatic crystals, whitish at the edges, in schist near St.
-Gothard, Switzerland. It is seldom cut.
-
-Kyanite is derived from its colour, κύανος blue, and disthene, from its
-variable hardness, δίς, twice, and σθένος, strong.
-
-
- ANDALUSITE
-
-Andalusite bears no resemblance whatever to kyanite, although, as has
-been stated above, the composition of the two species is essentially
-the same. It is usually light bottle-green in colour, and more rarely
-brown and reddish. Its extreme dichroism is its most remarkable
-character, the twin colours being olive-green and red. The reddish
-gleams that are reflected from the interior are in sharp contrast with
-the general colour of the stone, and impart to it a weird effect (Plate
-XXIX, Fig. 15). Cut stones are often confused with tourmalines, and
-can, indeed, only be distinguished from the latter with certainty by
-noting on the refractometer the smaller amount of double refraction
-and the difference in its character. The least and greatest of the
-refractive indices are 1·62 and 1·643 respectively, and the double
-refraction, 0·011, about half that of tourmaline, is biaxial and
-negative; the specific gravity is 3·18, and hardness 7½ on Mohs’s scale.
-
-Good stones are found at Minas Novas, Minas Geraes, Brazil, and in
-the gem-gravels of Ceylon. It was first known from the province of
-Andalusia, Spain, whence is the origin of its name.
-
-
- IDOCRASE
-
- (_Vesuvianite_, _Californite_)
-
-Idocrase, also known as vesuvianite, is occasionally found in the
-form of transparent, leaf-green, and yellowish-brown stones which,
-when cut, may be mistaken for diopside and epidote respectively, but
-are distinguishable from both by the extreme smallness of their
-double refraction. Californite is a compact variety which has all the
-appearances of a jade; its colour is green, or nearly colourless with
-green streaks.
-
-In composition idocrase is a silicate of aluminium and calcium, the
-precise formula of which is uncertain, but may be—
-
- (Ca,Mn,Mg,Fe)_{2}[(Al,Fe)(OH,F)]Si_{2}O_{7}.
-
-The double refraction, which is uniaxial in character and negative in
-sign, may be less than 0·001, and never exceeds 0·006, so that it is
-not easily detected with the refractometer, even in sodium light. The
-refractive indices vary enormously in value, from 1·702 to 1·726 for
-the ordinary, and from 1·706 to 1·732 for the extraordinary ray. The
-specific gravity varies from 3·35 to 3·45, and the hardness is about 6½
-on Mohs’s scale.
-
-The name idocrase, from εἴδος, form, and κρᾶσις, mixture, was assigned
-to the species by Haüy, but his reasons have little meaning at the
-present day. The other names are taken from the localities where the
-species and the variety were first discovered.
-
-Bright, green crystals come from Russia, and also from Ala Valley,
-Piedmont, and Mount Vesuvius, Italy. Californite is found in large
-masses in Siskiyon and Fresno Counties, California.
-
-
- EPIDOTE
-
- (_Pistacite_)
-
-Epidote often possesses a peculiar shade of yellowish green, similar
-to that of the pistachio-nut—hence the origin of its alternative
-name—which is unique among minerals, though scarcely pleasing enough
-to recommend it to general taste. Its ready cleavage renders it liable
-to flaws; nevertheless, it is occasionally faceted. The name epidote,
-from ἐπίδοσις, increase, was given to it by Haüy, but not on very
-precise crystallographical grounds.
-
-In composition this species is a silicate of calcium and aluminium,
-with some ferric oxide in place of alumina, corresponding to the
-complex formula, Ca_{2}(Al,Fe)_{2}[(Al,Fe)OH](SiO_{4})_{3}. It
-occurs in monoclinic, prismatic crystals richly endowed with natural
-faces. The colour deepens with increase in the percentage amount of
-iron, and the stones become almost opaque. The double refraction is
-large in amount, 0·031, biaxial in character, and negative in sign.
-The dichroism is conspicuous in transparent stones, the twin-tints
-corresponding to the principal optical directions being green, brown,
-and yellow. The values of the least and greatest of the refractive
-indices given by transparent stones are 1·735 and 1·766 respectively;
-the specific gravity varies from 3·25 to 3·50, and the hardness from 6
-to 7 on Mohs’s scale.
-
-Transparent crystals have come from Knappenwand, Untersulzbachtal,
-Salzburg, Austria; Traversella, Piedmont, Italy; and Arendal, Nedenäs,
-Norway. Magnificent, but very dark, crystals were discovered about ten
-years ago on Prince of Wales Island, Alaska.
-
-
- SPHENE
-
- (_Titanite_)
-
-The clear, green, yellow, or brownish stones provided by this species
-would be welcomed in jewellery because of their brilliant and
-almost adamantine lustre, but, unfortunately, they are too soft to
-withstand much wear, the hardness being only 5½ on Mohs’s scale. In
-composition sphene is a silico-titanate of calcium corresponding to
-the formula CaTiSiO_{5}, and in this respect comes near the recently
-discovered gem-stone, benitoite. The refractive indices lie outside
-the range of the refractometer, the values of the least and the
-greatest of the refractive indices varying from 1·888 and 1·917 to
-1·914 and 2·053 respectively. It is to this high refraction that it
-owes its brilliant lustre. The double refraction, which is biaxial in
-character and positive in sign, is so large that the apparent doubling
-of the opposite edges of a cut stone when viewed through one of the
-faces is obvious to the unaided eye (cf. p. 41). Cut stones have
-additional interest on account of the vivid dichroism displayed, the
-twin-tints, colourless, yellow, and reddish yellow, corresponding to
-the three principal optical directions, being in strong contrast. The
-specific gravity ranges from 3·35 to 3·45. The negative test with the
-refractometer (cf p. 26), the softness, and the large amount of double
-refraction suffice to distinguish this species from gem-stones of
-similar appearance.
-
-The name sphene, from σφήν, wedge, alludes to the shape of the natural
-crystals. The alternative name is obviously due to the fact that the
-species contains titanium.
-
-Good stones have come from the St. Gothard district, Switzerland.
-
-
- AXINITE
-
-Called axinite from the shape of its crystals—ἀξίνη, axe—this species
-supplies small, clear, clove-brown, honey-yellow, and violet stones
-which can be cut for those who care for a stone out of the ordinary.
-The composition is a boro-silicate of aluminium and calcium, with
-varying amounts of iron and manganese, corresponding to the formula
-(Ca,Fe)_{3}Al_{2}(B.OH)Si_{4}O_{15}. Axinite is interesting on
-account of its strong dichroism, the twin-tints corresponding to the
-principal optical directions being violet, brown, and green. The double
-refraction is biaxial in character and negative in sign, the least and
-greatest of the refractive indices being 1·674 and 1·684; the specific
-gravity is 3·28, and hardness about 6½ to 7, or rather under that of
-quartz.
-
-The best examples have been found at St. Cristophe, Bourg d’Oisans, in
-the Dauphiné, France. Violet axinite is a novelty that has come within
-recent years from Rosebery, Montagu County, Tasmania.
-
-
- PREHNITE
-
-This species, which is named after its discoverer, Colonel Prehn, is
-found in nodular, yellow and oil-green stones, of which the latter
-have very occasionally been cut. It is a little soft, the hardness
-being only 6 on Mohs’s scale. The double refraction is large in amount,
-0·033, biaxial in character, and positive in sign, the least and the
-greatest of the refractive indices being 1·616 and 1·649 respectively;
-the specific gravity varies from 2·81 to 2·95. In composition prehnite
-is a silicate of aluminium and calcium corresponding to the formula
-H_{2}Ca_{2}Al_{2}(SiO_{4})_{3}.
-
-The best material has been found at St. Cristophe, Bourg d’Oisans,
-Dauphiné, France.
-
-
- APATITE
-
-This interesting mineral is found occasionally in attractive green,
-blue, or violet stones, but is unfortunately too soft for extensive use
-in jewellery, the hardness being only 5 on Mohs’s scale. In composition
-it is a fluo-chloro-phosphate of calcium, corresponding to the formula
-Ca_{4}[Ca(F,Cl)](PO_{4})_{3}. When pure, it is devoid of colour,
-the tints being due to the presence of small amounts of tinctorial
-agents. The double refraction is uniaxial in character and negative in
-sign, the ordinary index being 1·642 and the extraordinary 1·646; the
-specific gravity varies from 3·17 to 3·23. The dichroism is usually
-feeble, but sometimes is strong; for instance, in the stones from the
-Burma ruby mines (yellow, blue-green). A cut stone might be mistaken
-for tourmaline, but is distinguished by its softness, or, when tested
-on the refractometer, by its inferior double refraction. It received
-its name from ἀπατάειν, deceive, because it was wrongly assigned to at
-least half a dozen different species in early days. Moroxite is a name
-sometimes given to blue-green apatite.
-
-Beautiful violet stones are found at Ehrenfriedersdorf, Saxony;
-Schlaggenwald, Bohemia; and Mount Apatite, Auburn, Androscoggin County,
-Maine, U.S.A.; and blue stones come from Ceylon.
-
-
- DIOPTASE
-
-Though of a pretty, emerald-green colour, dioptase has never been
-found in large enough crystals for gem purposes, and it is, moreover,
-rather soft, the hardness being only 5 on Mohs’s scale, and has an
-easy cleavage. In composition it is a hydrous silicate of copper
-corresponding to the formula CuH_{2}SiO_{4}. The double refraction,
-which is large in amount, is uniaxial in character, and positive in
-sign, the ordinary refractive index being 1·667 and the extraordinary
-1·723. Its colour and softness distinguish it from peridot or diopside,
-which have about the same refractivity. The name was assigned to the
-species by Haüy, from διὰ, through, and ὄπτομαι, see, because the
-cleavage directions were distinguishable by looking through the stone.
-
-Dioptase has been found near Altyn-Tübe in the Kirghese Steppes, at
-Rezbánya in Hungary, and Copiapo in Chili, and at the mine Mindouli,
-near Comba, in the French Congo.
-
-
-
-
- CHAPTER XXXVII
-
- CASSITERITE, ANATASE, PYRITES, HEMATITE
-
-
- CASSITERITE
-
-Though usually opaque, this oxide of tin, corresponding to the formula
-SnO_{2}, has occasionally, but very rarely, been found in small,
-transparent, yellow and reddish stones suitable for cutting. The lustre
-is adamantine. The refraction is uniaxial in character and positive
-in sign, the ordinary index being 1·997 and extraordinary 2·093. The
-specific gravity is high, ranging from 6·8 to 7·1. The hardness is on
-the whole less than that of quartz, being about 6 to 7 on Mohs’s scale.
-
-
- ANATASE
-
-This mineral, which is one of the three crystallized forms of titanium
-oxide, TiO_{2}, occurs often in small, brown, transparent stones which
-occasionally find their way into the market. The lustre is adamantine.
-The refraction is uniaxial in character and negative in sign, the
-extraordinary index being 2·493 and ordinary 2·554. The specific
-gravity varies from 3·82 to 3·95, and the hardness is about 5½ to 6 on
-Mohs’s scale.
-
-
- PYRITES, HEMATITE
-
-These two metallic minerals were employed in ancient jewellery. The
-former, sulphide of iron, FeS_{2}, is brass-yellow in colour, and has
-a specific gravity 5·2, and hardness 6½ on Mohs’s scale. It is found,
-when fresh, in brilliant cubes. The latter, oxide of iron, Fe_{2}O_{3},
-has a black metallic lustre, but, when powdered, is red in colour—a
-mode of distinguishing it from other minerals of similar appearance.
-Its specific gravity is 5·3, and hardness 6½ on Mohs’s scale. In modern
-times it has been cut in spherical form to imitate black pearls, but
-can easily be recognized by its greater density and hardness. Hematite
-is used for signet stones, often with an intaglio engraving.
-
-
-
-
- CHAPTER XXXVIII
-
- OBSIDIAN, MOLDAVITE
-
-
-Two forms of natural glass have been employed for ornamental purposes.
-Obsidian results from the solidification without crystallization of
-lava, and corresponds in composition to a granite. The structure
-is seldom clear and transparent, and usually contains inclusions
-or streaks. The colour is in the mass jet-black, but smoky in thin
-fragments, and occasionally greenish. Its property of breaking with a
-keen cutting edge, in the same way as ordinary glass, rendered it of
-extreme utility to primitive man, who was ignorant of the artificial
-substance. The refraction is, of course, single, and the refractive
-index approximates to 1·50. The specific gravity varies from 2·3 to
-2·5. The hardness is 5 on Mohs’s scale, the same as ordinary glass.
-
-Obsidian is obtained wherever there has been volcanic activity. Vast
-mines of great antiquity exist in the State of Hidalgo, Mexico.
-
-Moldavite, which differs in no respect from ordinary green
-bottle-glass, is of interest on account of its problematical origin.
-Its occurrence in various parts of Bohemia and Moravia cannot be
-explained as the result of volcanic agency. It may possibly be the
-product of old and forgotten glass factories which at one time existed
-on the site. Even meteorites have been suggested as the source. The
-physical characters are the same as those of ordinary glass: refraction
-single, index 1·51; specific gravity 2·50 and hardness 5½ on Mohs’s
-scale. Moldavite also passes under the names of bottle-stone, or
-water-chrysolite. A natural glass of the same character has been found
-in water-worn fragments in Ceylon, and has been sold as peridot, which
-it resembles in colour, but is readily distinguished from it by its
-very different physical properties.
-
-
-
-
- PART II—SECTION C
-
- ORNAMENTAL STONES
-
-
-
-
- CHAPTER XXXIX
-
- FLUOR, LAPIS LAZULI, SODALITE, VIOLANE, RHODONITE, AZURITE,
- MALACHITE, THULITE, MARBLE, APOPHYLLITE, CHRYSOCOLLA,
- STEATITE OR SOAPSTONE, MEERSCHAUM, SERPENTINE
-
-
-Space will not permit of more than a few words concerning the more
-prominent of the numerous mineral species which are employed for
-ornamental purposes in articles of virtu or in architecture, but which
-for various reasons cannot take rank as gem-stones.
-
-Fluor, a beautiful mineral which is found in its greatest perfection in
-England, has enjoyed well-deserved popularity when worked into vases
-or other articles. The finest material, deep purple in colour, known
-as ‘Blue John,’ came from Derbyshire, but the supply is now exhausted.
-The crystallized examples, from Durham, Devonshire, and Cornwall, form
-some of the most attractive of museum specimens. The crystals take the
-shape of cubes, often twinned, and have an easy octahedral cleavage.
-The refraction is single, the index being 1·433. Fluor is noted for its
-property of appearing of differing colour by reflected and transmitted
-light, and the phenomenon is in consequence known as fluorescence. The
-specific gravity is 3·18, and the hardness 4 on Mohs’s scale. Owing to
-its low refraction and softness, fluor is not suitable for jewellery.
-Clear colourless material is in demand for particular lenses of
-microscope objectives.
-
-The lovely blue stone known as lapis lazuli has since the earliest
-times been applied to all kinds of decorative purposes, for mosaic
-and inlaid work and as the material for vases, boxes, and so on, and
-was the original sapphire of the ancients. When ground to powder it
-furnishes a fine blue paint, but it has now been entirely superseded
-for this purpose by an artificial product. Although to the eye so
-homogeneous and uniform in structure, lapis lazuli has been shown
-by microscopic examination to be composed of calcite coloured by
-three blue minerals in varying proportions. All three belong to the
-cubic class of symmetry, and are mainly soda aluminium silicates
-in composition; their hardness varies from 5 to 6 on Mohs’s scale.
-Lazurite, Na_{4}(NaS_{3}.Al)Al_{2}Si_{3}O_{12}, has specific gravity
-varying from 2·38 to 2·45, and hardness about 5 to 5½; haüynite,
-(Na_{2},Ca)_{2}(NaSO_{4},Al)Al_{2}Si_{3}O_{12}, is about the same in
-specific gravity, 2·4 to 2·5, but slightly harder, 5½ to 6; while
-sodalite, Na_{4}(AlCl)Al_{2}Si_{3}O_{12}, is the lightest in density,
-2·14 to 2·30, with hardness 5½ to 6, and has a refractive index 1·483.
-
-By far the oldest mines are in the Badakshan district of Afghanistan,
-a few miles above Firgamu in the valley of the Kokcha, a branch of
-the Oxus, where ruby and spinel are found. It is also found at the
-southern end of Lake Baikal, Siberia, and in the Chilian Andes.
-
-Sodalite occurs in beautiful blue masses at Dungannon, Hastings County,
-Ontario, Canada, and at Litchfield, Maine, U.S.A. They make excellent
-polished stones.
-
-Violane, a massive, dark violet-blue diopside from San Marcel,
-Piedmont, Italy, also makes a handsome polished stone.
-
-Rhodonite, silicate of manganese, MnSiO_{3}, possesses a fine red
-colour, and makes an attractive stone when cut and polished. It has
-very slight biaxial double refraction, the refractivity being about
-1·73; the specific gravity is 3·6, and hardness 6. It is found in large
-masses near Ekaterinburg in the Ural Mountains, and is quarried as an
-ornamental stone.
-
-Both the copper carbonates, azurite or chessylite, and malachite, make
-effective polished stones. The latter is also worked into various
-ornamental objects; it occurs in fibrous masses, the grained character
-of which look well in the polished section. Its colour is a bright
-green, to which it owes its name, from μαλακή, mallows. Its composition
-is represented by the formula CuCO_{3}.Cu(OH)_{2}, and it is the more
-stable form, since azurite is frequently found altered to it. It
-has biaxial double refraction, and the indices are about 1·88; the
-specific gravity is 4·01, and hardness about 3½ to 4 on Mohs’s scale.
-It is found in large masses at the copper mines of Nizhni Tagilsk in
-the Ural Mountains, where it is mined as an ornamental stone; it also
-accompanies the copper ores in many parts of the world, for instance
-Cuba, Chili, and Australia. Azurite, so called on account of its
-beautiful blue colour, is rarer, but, unlike malachite, is generally in
-the form of crystals. Beautiful specimens have come from Chessy, near
-Lyons, France, and Bisbee, Arizona, U.S.A. The composition corresponds
-to the formula 2CuCO_{3}, Cu(OH)_{2}. The specific gravity is 3·80, and
-hardness about 3½ to 4.
-
-Chrysocolla occurs in blue and bluish-green earthy masses, with
-an enamel-like texture, which in some instances can be worked and
-polished. Being the result of the decomposition of copper ores, it
-varies considerably in hardness, ranging from 2 to 4 on Mohs’s scale.
-Its composition approaches to the formula CuSiO_{3}.2H_{2}O, but it
-invariably contains impurities. It is very light, the density being
-only about 2·2.
-
-Steatite, or soapstone, is a massive foliated silicate of magnesium
-corresponding to the formula H_{2}Mg_{3}Si_{4}O_{12}, which is one of
-the softest of mineral substances, representing the degree 1 on Mohs’s
-scale, but in massive pieces is harder owing to the intermixture of
-other substances with it. It has a peculiar greasy feeling to the
-touch, due to its softness. The specific gravity is about 2·75. The
-Chinese carve images out of the yellowish and brownish pieces.
-
-Meerschaum, a silicate of magnesium corresponding to the formula
-H_{4}Mg_{2}Si_{3}O_{10}, is familiar to every smoker as a material for
-pipe-bowls. It is very light, the specific gravity being only 2·0, and
-soft, the hardness being about 2 to 2½ on Mohs’s scale. When found,
-it is pure white in colour, and answers to its name, a German word
-signifying sea-foam. It comes from Asia Minor.
-
-Serpentine has been largely used for decorative purposes, as well
-as for cameos and intaglios, and formed most of the famous ‘verde
-antique.’ Being the result of the decomposition of other silicates
-it varies enormously in appearance and characters, but the most
-attractive stones are a rich oil-green in colour and resemble jade. The
-composition approximates to the formula H_{4}Mg_{3}Si_{2}O_{9}, but it
-invariably contains other elements. The hardness varies from 2½ to 4
-on Mohs’s scale, according to the minerals contained in the stone; the
-specific gravity is about 2·60 and the refractivity 1·570.
-
-The beautiful rose-red stone, thulite, makes a handsome decorative
-stone. It has nearly the same composition as epidote (p. 275), and like
-it has strong dichroism, the principal colours being yellow, light
-rose, and deep rose. The colour is due to manganese. Its refractive
-index is about 1·70, specific gravity 3·12, and hardness 6 to 6½ on
-Mohs’s scale; it possesses an easy cleavage. Fine specimens come from
-Telemark, Norway, and it is therefore called after the old name for
-Norway, Thule.
-
-Marble is a massive calcite, carbonate of lime, with the formula
-CaCO_{3}. When pure it is white, but it is usually streaked with other
-substances which impart a pleasing variety to its appearance. It is
-always readily recognized by the immediate effervescence set up when
-touched with a drop of acid. Calcite is highly doubly refractive (cf.
-p. 40), the extraordinary index being 1·486, and ordinary 1·658, a
-difference of 0·172; the specific gravity is 2·71, and hardness 3 on
-Mohs’s scale. Lumachelle, or fire-marble, is a limestone containing
-shells from which a brilliant, fire-like chatoyancy is emitted
-when light is reflected at the proper angle. It sometimes resembles
-opal-matrix, but is easily distinguished by its lower hardness and by
-its effervescent action with acid. Choice specimens come from Bleiberg
-in Carinthia, and from Astrakhan.
-
-Apophyllite has not many characters to commend it, being at the best
-faintly pinkish in colour, and always imperfectly transparent. It is
-a hydrous silicate of potassium and calcium with the complex formula
-(H,K)_{2}Ca(SiO_{3})_{2}.H_{2}O. Its refractivity is about 1·535,
-specific gravity 2·5, and hardness 4½ on Mohs’s scale; it possesses
-an easy cleavage. It occurs in the form of tetragonal crystals at
-Andreasberg in the Harz Mountains, and in the Syhadree Mountains,
-Bombay, India.
-
-
-
-
- PART II—SECTION D
-
- ORGANIC PRODUCTS
-
-
-
-
- CHAPTER XL
-
- PEARL, CORAL, AMBER
-
-
-Although none of the substances considered in this chapter come within
-the strict definition of a stone, since they are directly the result of
-living agency, yet pearl at least cannot be denied the title of a gem.
-Both pearl and coral contain calcium carbonate in one or other of its
-crystallized forms, and both are gathered from the sea; but otherwise
-they have nothing in common. Amber is of vegetable origin, and is a
-very different substance.
-
-
- PEARL
-
-From that unrecorded day when some scantily clothed savage seeking for
-succulent food opened an oyster and found to his astonishment within
-its shell a delicate silvery pellet that shimmered in the light of a
-tropical sun, down to the present day, without intermission, pearl has
-held a place all its own in the rank of jewels. Though it be lacking in
-durability, its beauty cannot be disputed, and large examples, perfect
-in form and lustre, are sufficiently rare to tax the deepest purse.
-
-The substance composing the pearl is identical with the iridescent
-lining—mother-o’-pearl or nacre, as it is termed—of the shell.
-Tortured by the intrusion of some living thing, a boring parasite,
-a worm, or a small fish, or of a grain of sand or other inorganic
-substance, and without means to free itself, the mollusc perforce
-neutralizes the irritant matter by converting it into an object of
-beauty that eventually finds its way into some jewellery cabinet. Built
-up in a haphazard manner and not confined by the inexorable laws of
-intermolecular action, a pearl may assume any and every variety of
-shape from the regular to the fantastic. It may be truly spherical,
-egg- or pear-shaped—pear-drops or pear-eyes, as they are termed—or it
-may be quite irregular—the so-called baroque or barrok pearls. The
-first is the most prized, but a well-shaped drop-pearl is in great
-demand for pendants or ear-rings. The colour is ordinarily white, or
-faintly tinged yellowish or bluish, and somewhat rarely, salmon-pink,
-reddish, or blackish grey. Perfect black pearls are valuable, but not
-as costly as the finest of the white. Though not transparent, pearl is
-to a varying extent translucent, and its characteristic lustre—‘orient’
-in the language of jewellery—is due to the same kind of interaction
-of light reflected from different layers that has been remarked upon
-in the case of opal and certain other stones. The translucency varies
-in degree, and some jewellers speak of the ‘water’ of pearls just as
-in the case of diamonds. If a pearl be sliced across the middle and
-the section be examined under the microscope, it will be seen that
-the structure consists of concentric shells and resembles that of an
-onion. These shells are alternately composed of calcium carbonate in
-its crystallized form, aragonite, and of a horny organic matter known
-as conchiolin, and they evidently represent the result of intermittent
-growth. Because of their composite character, pearls have a specific
-gravity ranging from 2·65 to 2·69-2·84-2·89 in the case of pink
-pearls—which is appreciably less than that of aragonite, 2·94: the
-hardness is about the same, namely, 3½ to 4 on Mohs’s scale. That the
-arrangement of the mineral layers is approximately parallel is evinced
-by the distinctness of the shadow-edges shown on examination with the
-refractometer. Pearls require very careful handling, both because they
-are comparatively soft and therefore apt to be scratched, and because
-they are chemically affected by acids, and even by the perspiration
-from the skin. Acids attack only the calcium carbonate, not the
-organic matter; the well-known story therefore of Cleopatra dissolving
-a valuable pearl in vinegar, which is moreover, too weak an acid to
-effect the solution quickly, must not be accepted too literally.
-Pearls are not cut like stones, and therefore as soon as the precious
-bloom has once gone, nothing can be done to revive it. Attempts are
-sometimes made in the case of valuable pearls to remove the dull skin
-and lay bare another iridescent layer underneath, but the operation is
-exceedingly delicate. Even with the best of care pearls must in process
-of time perish owing to the decay of the organic constituent. Pearls
-that have been discovered in ancient tombs crumbled to dust at a touch,
-and those formerly in ancient rings have vanished or only remain as
-a brown powder, while the garnets or other stones set with them are
-little the worse for the centuries that have passed by.
-
-The largest known pearl was at one time in the famous collection
-belonging to the banker, Henry Philip Hope. Cylindrical in form, with
-a slight swelling at one end, it measures 50 mm. (2 inches) in length,
-and 115 mm. (4½ inches) in circumference about the thicker, and 83
-mm. (3¼ inches) about the thinner end, and weighs 454 carats. About
-three-quarters of it is white in colour with a fine ‘orient,’ and the
-remainder is bronze in tint. It is valued at upwards of £12,000. A
-large pearl, 300 carats in weight, is in the imperial crown of the
-Emperor of Austria, and another, pear-shaped, is in the possession of
-the Shah of Persia. A beautiful white India pearl, a perfect sphere in
-shape, and 28 carats in weight, is in the Museum of Zosima in Moscow;
-it is known as ‘La Pellegrina.’ The ‘Great Southern Cross,’ which
-consists of nine large pearls naturally joined together in the shape of
-a cross, was discovered in an oyster fished up in 1886 off the beds of
-Western Australia. The collection of jewels in the famous Green Vaults
-at Dresden contains a number of pearls of curious shapes.
-
-Large pearls are sold separately, while the small pearls known as
-‘seed’ pearls come into the market bored and strung on silk in
-‘bunches.’ The unit of weight is the pearl grain, which is a quarter
-of a carat, and the rate of price depends on the square of the weight
-in grains. The rate per unit or base varies from 6d. to 50s. according
-to the shape and quality of the pearl. Spherical pearls command the
-best prices, next the pearl-drops, and lastly the buttons; but whatever
-the shape, it is imperative that the pearl have ‘orient,’ without which
-it is valueless. The cheaper grades of pearls are sold by the carat.
-
-[Illustration: _PLATE XXX_
-
-NATIVES DRILLING PEARLS]
-
-For use in necklaces and pendants pearls are bored with a steel drill,
-and threaded with silk, an easy operation on account of their softness.
-They harmonize well with diamonds. Small pearls are often set as a
-frame to large coloured stones, to which they form an admirable foil.
-Pearls set in rings or anywhere where the upper half alone would show
-are generally sawn in halves; ‘button’ pearls find an extensive use in
-modern rings.
-
-Any mollusc, whether of the bi-valve or the uni-valve type, which
-possesses a nacreous shell, has the power of producing pearls,
-but only two, the pearl-oyster, _Meleagrina margaritifera_, and
-the pearl-mussel, _Unio margarifer_, repay the cost of systematic
-fishing. The outside of the shell is formed of the horny matter called
-conchiolin; while the inside is composed of two coats, of which
-the outer consists of alternate layers of conchiolin and calcium
-carbonate in its crystallized form, calcite, and the inner of the same
-organic matter, but with calcium carbonate in its other crystallized
-form, aragonite. The latter coat forms the nacreous lining known as
-mother-o’-pearl, which is identical in consistency with pearl, but
-somewhat more transparent. The iridescence of mother-o’-pearl is due
-not only to the fact that it is composed of a succession of thin
-translucent layers, but also to the fact that these layers overlap
-like slates on a house, and form a series of fine parallel lines on
-the surface; diffraction therefore as well as interference of light
-takes place, and a similar diffraction phenomenon is displayed even
-by a cast of the inside of the shell. The animal has the property of
-secreting calcium carbonate, which it absorbs from the sea-water, in
-both its crystallized conditions as well as conchiolin. At the outer
-rim it secretes conchiolin, further in calcite, and at the very inside
-aragonite. The shape and appearance of a pearl therefore depend on
-the position in which the intruding substance is situated within the
-shell. The most perfect pearl has been in intermittent motion in the
-interior of the mollusc, and has received successive coats according
-to the position in which it happened to be. A parasite that bores
-into the shell is walled up at the point of entrance, and a wart- or
-blister-pearl results. The thinner the successive coats the finer
-the lustre. Pearls have even been discovered embedded in the animal
-itself. The number of pearls found in a shell depends on the number of
-times the living host was compelled to seal up some irritant object,
-and may vary from one up to the eighty-seven which are said to have
-been found in an Indian oyster. That an oyster thus distinguished has
-not led a happy existence is testified by the distorted shape of its
-shell, a clue that guides the pearl-fishers in their search. Moreover,
-pearl-oysters never have thick nacreous shells, and on the other hand
-molluscs with fine mother-o’-pearl seldom contain pearls.
-
-Beautiful white and silvery pearls are found in a small oyster that
-lives at a depth of 6 to 13 fathoms (11-24 m.) in the Gulf of Manaar,
-off the coast of Ceylon. About seven-eighths, however, of the pearls
-that come into the market are obtained from a larger oyster which
-has its home on the Arabian coast of the Persian Gulf. These famous
-fisheries have been known since very early times. The pearls found
-here are more yellowish than those from Ceylon, but are nevertheless
-of excellent quality. The pearl fisheries off the north-west coast of
-Western Australia and off Venezuela are also not unimportant, and fine
-black pearls have been supplied by molluscs from the Gulf of Mexico.
-
-[Illustration: _PLATE XXXI_
-
-METAL FIGURES OF BUDDHA INSERTED IN A PEARL-OYSTER]
-
-[Illustration: _PLATE XXXII_
-
-FIG. 1
-
-FIG. 2
-
-SECTIONS OF CULTURE PEARL
-
-FIG. 1. IN THE OYSTER. FIG. 2. WHEN FINISHED.
-
-A. PEARLY DEPOSIT. B. PIECE OF MOTHER-O’-PEARL INSERTED IN THE OYSTER.
-C. OUTER SHELL OF THE OYSTER. D. MOTHER-O’-PEARL BACK ADDED.]
-
-The Chinese have long made a practice of introducing into the shell of
-a pearl-oyster little tin images of Buddha in order that they may be
-coated with the nacreous secretion. The Japanese have during recent
-years made quite an industry of stimulating the efforts of the mollusc
-by cementing small pieces of mother-o’-pearl to the interior surface
-of the shell (Plate XXXII, Fig. 1); these ‘culture’ pearls, as they
-are termed, are recognizable by examination of the back. About a year
-has to elapse before a coating of a tenth of a millimetre is formed,
-and another two years must pass before the thickness is doubled. After
-removal the piece of mother-o’-pearl, which is now coated with several
-nacreous layers, is cemented to a piece of ordinary mother-o’-pearl,
-and the lower portion is ground to the usual symmetrical shape (Plate
-XXXII, Fig. 2). Blister pearls are often similarly treated. In both
-cases, however, the ‘orient’ is deficient in quality.
-
-The finest mother-o’-pearl is supplied by a mollusc found in the sea
-near the islands lying between Borneo and the Philippines, and fine
-material is found at Shark Bay and off Thursday Island.
-
-
- CORAL
-
-Coral ranks far below pearl and meets with but limited appreciation.
-It is common enough in warm seas, but the only kind which finds its
-way into jewellery is the rose or red-coloured coral—the noble coral,
-_Corallium nobile_ or _rubrum_. It consists of the axial skeleton of
-the coral polyp, and is built up of hollow tubes fitting one within
-the other. The composition is mainly calcium carbonate with a little
-magnesium carbonate and a small amount of organic matter. The former
-of the mineral substances is in the form of calcite, and the crystals
-are arranged in fibrous form radiating at right angles to the axis of
-the coral. The specific gravity varies from 2·6 to 2·7, being slightly
-under that of calcite, and the hardness is somewhat greater, being
-about 3¾ on Mohs’s scale.
-
-The best red coral is found in the Mediterranean Sea off Algiers and
-Tunis in Africa, and Sicily and the Calabrian Coast of Italy. The
-industry of shaping and fashioning the coral is carried on almost
-entirely in Italy. Coral is usually cut into beads, either round or
-egg-shaped, and used for necklaces, rosaries, and bracelets. The best
-quality fetches from 20s. to 30s. per carat.
-
-
- AMBER
-
-This fossil resin, yellow and brownish-yellow in tint, finds an
-extensive use as the material for mouthpieces of pipes, cigar and
-cigarette-holders, umbrella-handles, and so on, and is even locally
-cut for jewellery, although its extreme softness, its hardness being
-only 2½ on Mohs’s scale, quite unfits it for such a purpose. It is
-only slightly denser than water, the specific gravity being about
-1·10. Since the structure is amorphous the refraction is single, the
-index being about 1·540. Amber, being a very bad conductor of heat, is
-perceptibly warm to the touch. Its property of becoming electrified by
-friction attracted early attention, and from the Greek name for it,
-ἤλεκτρον, is derived our word electricity.
-
-Amber is washed up by the sea off the coasts of Sicily and Prussia,
-and of Norfolk and Suffolk in England. The finest examples, which are
-picked up off the shore of Catania in Sicily, are distinguished by a
-fine bluish fluorescence, resembling that seen in lubricating oil; such
-pieces command good prices.
-
-A recent resin, pale yellow in colour, known as kauri-gum, is found in
-New Zealand, where it is highly valued.
-
-
-
-
- TABLES
-
-
- TABLE I
-
- _Chemical Composition of Gem-Stones_
-
- (_a_) ELEMENTS—
-
- Diamond C
-
- (_b_) OXIDES—
-
- Corundum Al_{2}O_{3}
- Quartz SiO_{2}
- Chalcedony SiO_{2}
- Opal SiO_{2}.nH_{2}O
-
- (_c_) ALUMINATES—
-
- Spinel MgAl_{2}O_{4}
- Chrysoberyl BeAl_{2}O_{4}
-
- (_d_) SILICATES—
-
- Phenakite Be_{2}SiO_{4}
- Dioptase H_{2}CuSiO_{4}
- Peridot Mg_{2}SiO_{4}
- Zircon ZrSiO_{4}
- Enstatite MgSiO_{3}
- Diopside CaMg(SiO_{3})_{2}
- Nephrite CaMg_{3}(SiO_{3})_{4}
- Sphene CaTiSiO_{5}
- Benitoite BaTiSi_{3}O_{9}
- Andalusite Al(AlO)SiO_{4}
- Kyanite (AlO)_{2}SiO_{3}
- Topaz [Al(F,OH)]_{2}SiO_{4}
- Epidote Ca_{2}(Al,Fe)_{2}(AlOH)(SiO_{4})_{3}
- Euclase Be(AlOH)SiO_{4}
- Prehnite H_{2}Ca_{2}Al_{2}(SiO_{4})_{3}
- Iolite H_{2}(Mg,Fe)_{4}Al_{8}Si_{10}O_{37}
- { Hessonite Ca_{3}Al_{2}(SiO_{4})_{3}
- _Garnet_ { Pyrope Mg_{3}Al_{2}(SiO_{4})_{3}
- { Almandine Fe_{3}Al_{2}(SiO_{4})_{3}
- { Andradite Ca_{3}Fe_{2}(SiO_{4})_{3}
- Beryl Be_{3}Al_{2}(SiO_{3})_{6}
- Spodumene LiAl(SiO_{3})_{2}
- Jadeite NaAl(SiO_{3})_{2}
- Moonstone KAlSi_{3}O_{8}
- Tourmaline{12SiO_{2}.3B_{2}O_{3}.(9-x)[(Al,Fe)_{2}O_{3}].3x[
- {(Fe,Mn,Ca,Mg,K_{2},Na_{2},Li_{2},H_{2})O].3H_{2}O
- Axinite HCa_{3}Al_{2}B(SiO_{4})_{4}
- Idocrase (Ca,Mn,Mg,Fe)_{2}(Al,Fe)(OH,F)]Si_{2}O_{7}
-
- (_e_) PHOSPHATES—
-
- Beryllonite NaBePO_{4}
- Apatite Ca_{5}(F,Cl)(PO_{4})_{3}
- Turquoise CuOH.6[Al(OH)_{2}].H_{5}.(PO_{4})_{4}
-
-
- TABLE II
-
- _Colour of Gem-Stones_
-
- _Colourless and White._—Diamond, corundum (white sapphire), topaz,
- quartz (rock-crystal), zircon (when ‘fired’), moonstone; rarely
- beryl, tourmaline; among the less common species, phenakite,
- spodumene (colourless kunzite), beryllonite.
-
- _Yellow._—Diamond, topaz, corundum (yellow sapphire), quartz
- (citrine, Scotch or occidental topaz), tourmaline, zircon,
- sphene, spodumene, beryl.
-
- _Pink and Lilac._—Corundum (pink sapphire), spinel (balas-ruby),
- tourmaline (rubellite), topaz (usually when ‘fired’), spodumene
- (kunzite), beryl (morganite), quartz (rose-quartz).
-
- _Red._—Corundum (ruby), garnet (pyrope, almandine), spinel
- (balas-ruby), tourmaline (rubellite), zircon, opal (fire-opal).
-
- _Green._—Beryl (emerald, aquamarine), peridot, corundum,
- tourmaline, chrysoberyl (including alexandrite), zircon, garnet
- (demantoid); among less common species, spodumene (hiddenite),
- euclase, diopside, idocrase, epidote, apatite, obsidian; rarely
- diamond; also semi-opaque, turquoise, jade.
-
- _Blue._—Corundum (sapphire), spinel, topaz, tourmaline, zircon;
- among the less common species, kyanite, iolite, benitoite,
- apatite; rarely diamond; also semi-opaque, turquoise, lapis
- lazuli, sodalite.
-
- _Violet and Purple._—Quartz (amethyst), corundum (oriental
- amethyst), spinel (almandine-spinel), garnet (almandine),
- spodumene (kunzite), apatite.
-
- _Brown._—Diamond, tourmaline, quartz (smoky-quartz); among the less
- common species, andalusite, axinite, sphene.
-
-
- TABLE III
-
- _Refractive Indices of Gem-Stones_[8]
-
- Opal 1·454
- Moonstone 1·53 1·54
- Iolite 1·543 1·551
- Quartz 1·544 1·553
- Beryllonite 1·553 1·565
- Beryl 1·578 1·585
- Turquoise 1·61 1·65
- Topaz 1·618 1·627
- Andalusite 1·632 1·643
- Tourmaline 1·626 1·651
- Apatite 1·642 1·646
- Phenakite 1·652 1·667
- Euclase 1·651 1·670
- Spodumene 1·660 1·675
- Enstatite 1·665 1·674
- Peridot 1·659 1·697
- Axinite 1·674 1·684
- Diopside 1·685 1·705
- Idocrase 1·714 1·719
- Spinel 1·726
- Kyanite 1·72 1·73
- Epidote 1·735 1·766
- Garnet (Hessonite) 1·745
- Chrysoberyl 1·746 1·753
- Garnet (Pyrope) 1·755
- Benitoite 1·757 1·804
- Corundum 1·761 1·770
- Garnet (Almandine) 1·790
- Zircon (a) 1·815
- Garnet (Demantoid) 1·885
- Sphene 1·901 1·985
- Zircon (b) 1·927 1·980
- Diamond 2·417
-
-
- TABLE IV
-
- _Colour-Dispersion of Gem-Stones_[9]
-
- Moonstone ·012
- Quartz ·013
- Beryl ·014
- Topaz ·014
- Chrysoberyl ·015
- Tourmaline ·017
- Spodumene ·017
- Corundum ·018
- Peridot ·020
- Spinel ·020
- Garnet (Almandine) ·024
- Garnet (Pyrope) ·027
- Garnet (Hessonite) ·028
- Zircon ·038
- Diamond ·044
- Sphene ·051
- Garnet (Demantoid) ·057
-
-
- TABLE V
-
- _Character of the Refraction of Gem-Stones_
-
-
- (_a_) SINGLE—
-
- Diamond, spinel, garnet, opal.
- Diamond and garnet frequently display local double refraction.
-
- (_b_) UNIAXIAL, POSITIVE—
-
- Quartz ·009
- Phenakite ·015
- Benitoite ·047
- Zircon (b) ·053
- Quartz exhibits circular polarization.
-
- (_c_) UNIAXIAL, NEGATIVE—
-
- Apatite ·004
- Idocrase ·005
- Beryl ·007
- Corundum ·009
- Tourmaline ·025
-
- (_d_) BIAXIAL, POSITIVE—
-
- Chrysoberyl ·007
- Topaz ·009
- Enstatite ·009
- Spodumene ·015
- Euclase ·019
- Diopside ·020
- Peridot ·038
- Sphene ·084
-
- (_e_) BIAXIAL, NEGATIVE—
-
- Moonstone ·006
- Iolite ·008
- Axinite ·010
- Andalusite ·011
- Beryllonite ·012
- Kyanite ·016
- Epidote ·031
-
-
- TABLE VI
-
- _Dichroism of Gem-Stones_
-
- (_a_) STRONG
-
- Corundum, tourmaline, alexandrite, spodumene, andalusite, iolite,
- epidote, axinite.
-
- (_b_) DISTINCT
-
- Emerald, topaz, quartz, peridot, chrysoberyl, enstatite, euclase,
- idocrase, kyanite, sphene, apatite.
-
- (_c_) WEAK
-
- Beryl, diopside.
-
-
- TABLE VII
-
- _Specific Gravities of Gem-Stones_
-
- Opal 2·15
- Moonstone 2·57
- Iolite 2·63
- Quartz 2·66
- Beryl 2·74
- Turquoise 2·82
- Beryllonite 2·84
- Phenakite 2·99
- Euclase 3·07
- Tourmaline 3·10
- Enstatite 3·10
- Andalusite 3·18
- Spodumene 3·18
- Apatite 3·20
- Axinite 3·28
- Diopside 3·29
- Epidote 3·37
- Peridot 3·40
- Idocrase 3·40
- Sphene 3·40
- Diamond 3·52
- Topaz 3·53
- Spinel 3·60
- Kyanite 3·61
- Garnet (Hessonite) 3·61
- Benitoite 3·64
- Chrysoberyl 3·73
- Garnet (Pyrope) 3·78
- Garnet (Demantoid) 3·84
- Corundum 4·03
- Garnet (Almandine) 4·05
- Zircon (a) 4·20
- Zircon (b) 4·69
-
-
- TABLE VIII
-
- _Degrees of Hardness of Gem-Stones_
-
- 5. Kyanite (5-7), apatite, lapis lazuli
- 5½. Enstatite, beryllonite, sphene
- 6. Opal, moonstone, turquoise, diopside
- 6½. Spodumene, peridot, garnet (demantoid), benitoite, idocrase,
- epidote, axinite, jade (nephrite)
- 7. Iolite, quartz, tourmaline, jade (jadeite)
- 7¼. Garnet (hessonite, pyrope)
- 7½. Beryl, garnet (almandine), zircon, phenakite, euclase, andalusite
- 8. Topaz, spinel
- 8½. Chrysoberyl
- 9. Corundum
- 10. Diamond
-
-
- TABLE IX.—DATA
-
- _Densities of Water and Toluol at Ordinary Temperatures_
-
- +-----------------------------+----------+----------+
- | TEMPERATURE | WATER | TOLUOL |
- +-----------------------------+----------+----------+
- | Centigrade | Fahrenheit | | |
- | | | | |
- | 14° | 57·2° | 0·9994 | 0·8697 |
- | 15° | 59·0° | 0·9992 | 0·8687 |
- | 16° | 60·8° | 0·9990 | 0·8677 |
- | 17° | 62·6° | 0·9988 | 0·8667 |
- | 18° | 64·4° | 0·9986 | 0·8657 |
- | 19° | 66·2° | 0·9985 | 0·8647 |
- | 20° | 68·0° | 0·9983 | 0·8637 |
- | 21° | 69·0° | 0·9981 | 0·8627 |
- | 22° | 71·6° | 0·9979 | 0·8617 |
- | 23° | 73·4° | 0·9977 | 0·8607 |
- +-----------------------------+----------+----------+
-
- 1 English carat = 0·2053 gram
- 1 Metric carat = 0·2000 (one-fifth) gram
- 1 oz. Av. = 28·35 grams
- 1 lb. Av. = 0·4536 kilogram
- 1 inch = 25·4 millimetres
- 1 foot = 0·3048 metre
- 1 yard = 0·9144 metre
- 1 mile = 1·6093 kilometre
-
-
-
-
- INDEX
-
-
- Absorption, 53, 59
-
- Absorption spectra, 59
-
- Achroite, 220, 221
-
- Adularia, 255
-
- Agate, 247
-
- Akbar Shah diamond, 163
-
- Alalite, 272
-
- Albite, 254
-
- Alexandrite, 54, 60, 233
- Scientific, 122
-
- Almandine, 60, 214
- Oriental, 112, 172
- spinel, 112, 204
-
- Amazon-stone, 255
-
- Amber, 83, 298
-
- Amethyst, 239, 242
- Oriental, 111, 172, 239
-
- Anatase, 281
-
- Andalusite, 274
-
- Andradite, 216
-
- Anomalous refraction, 47
-
- Anorthite, 254
-
- Apatite, 279
-
- Apophyllite, 290
-
- Aquamarine, 184, 193
-
- Arizona-ruby, 213
-
- Artificial stones, 124
-
- Asteria, 38, 177
-
- Asterism, 38
-
- Australia stones, 154, 174, 182, 195, 213, 216, 227, 232, 252,
- 288
-
- Austrian Yellow diamond, 165
-
- Aventurine, 240, 241
-
- Axes, Crystallographic, 9
- Optic, 49
-
- Axinite, 278
-
- Azure-quartz, 244
-
- Azurite, 287
-
-
- Balas-ruby, 203
-
- Barnato, Barnett, 145
-
- Baroque, Barrok, pearls, 292
-
- Bastite, 272
-
- Benitoite, 267
-
- Berquem, Louis de, 90, 161
-
- Beryl, 184
-
- Beryllonite, 270
-
- Bezel facet, 92
-
- Biaxial double refraction, 45, 49, 57
-
- Bisectrix, 45, 49
-
- Black diamond, 129
-
- Black lead, 129
-
- Black opal, 249, 250
-
- Black Prince’s ruby, 206
-
- Blister-pearl, 296
-
- Bloodstone, 247
-
- Blue felspar, 255
-
- Blue ground, 143, 147
-
- Blue John, 285
-
- Boart, 103, 129, 133
-
- Bohemian garnet (pyrope), 207, 212
-
- Bone turquoise, 259
-
- Boodt, A. B. de, 132, 213
-
- Borgis, Hortensio, 161
-
- Borneo stones, 154, 170
-
- Bort, _v._ Boart, 103, 129, 133
-
- Bottle-stone, 284
-
- Boule, 118
-
- Bowenite, 263
-
- Braganza diamond, 170
-
- Brazil stones, 138, 165, 166, 169, 194 _et seq._, 201, 215, 223,
- 236, 243, 244, 248, 266, 269, 270, 274
-
- Brazilian emerald, 111, 220, 221
- peridot, 221
- sapphire, 111, 221
- topaz, 111, 197
-
- Brilliant form of cutting, 92
-
- Brilliant, Scientific, 122
-
- Bristol diamonds, 243
-
- Bruting, 100
-
- Burma stones, 178, 205, 223, 227, 263
-
- Button-pearl, 295
-
- Byes, Bywaters, 136, 150
-
-
- Cabochon form of cutting, 88
-
- Cacholong, 251
-
- Cairngorm, 239
-
- Callaica, callaina, callais, 258
-
- Calcite, 40, 289
-
- California stones, 156, 195, 202, 224, 259, 265, 267, 275
-
- Californite, 264, 275
-
- Cape-ruby, 213
-
- Carat weight, 72, 84
-
- Carbon, 129
-
- Carbonado, 129
-
- Carborundum, 105
-
- Carbuncle, 89, 215
-
- Carnelian, 247
-
- Cascalho, 139
-
- Cassiterite, 281
-
- Cat’s-eye (chrysoberyl), 38, 90, 233
- (quartz), 39, 90, 240
- (tourmaline), 39, 219
- Hungarian, 244
-
- Ceylon stones, 181, 195, 201, 205, 212, 215, 216, 223, 232, 236,
- 237, 243, 244, 255, 267, 274, 279, 284
-
- Ceylonese peridot (tourmaline), 221
-
- Ceylonite, 204
-
- Chalcedony, 246
-
- Chatoyancy, 38
-
- Chert, 247
-
- Chessylite, 287
-
- Chrysoberyl, 233
-
- Chrysocolla, 288
-
- Chrysolite (chrysoberyl), 233
- (peridot), 225
-
- Chrysoprase, 247
-
- Church, Sir Arthur, 61, 211, 231
-
- Cinnamon-stone, 211
-
- Citrine, 239
-
- Cleavage, 80, 100, 149
-
- Close goods, 149
-
- Colenso diamond, 131
-
- Colour, 53
-
- Colour dispersion, 20, 97
-
- Conchiolin, 293
-
- Coral, 298
-
- Cordierite, 266
-
- Cornish diamonds, 243
-
- Corundum, 172
-
- Crocidolite, 39, 240
-
- Crookes, Sir William, 132, 153
-
- Cross facet, 93
-
- Crystal, 6, 7, 8
- Rock-, 97
-
- Cubic system, 8
-
- Culet facet, 93
-
- Cullinan diamond, 94, 100, 168
-
- Culture pearls, 297
-
- Cumberland diamond, 164
-
- Cyanite (Kyanite), 79, 273
-
- Cymophane, 234
-
-
- Darya-i-nor diamond, 162
-
- De Beers diamonds, 167
-
- Demantoid, 216
-
- Density, 63
-
- Deviation, Minimum, 30
-
- Diamond, Characters of, 128
- cutting, 90
- gauges, 86
- Glaziers’, 135
- mining, 146
- Occurrence of, in—
- Borneo, 154
- Brazil, 139
- German South-West Africa, 155
- India, 138
- New South Wales, 154
- Rhodesia, 155
- South Africa, 139
- Origin of, 151
- -point, 91
- -rose, 92
- -table, 91
-
- Diamonds, Classification of, 136, 149
- Historical, 157
- Prices of, 135
-
- Dichroism, 55
-
- Dichroite, 266
-
- Dichroscope, 55
-
- Diffusion column, 65
-
- Diopside, 272
-
- Dioptase, 280
-
- Dispersion, Colour, 20, 24, 97
-
- Disthene, 273
-
- Dop, 102
-
- Double refraction, 28, 40
-
- Doublet, 125
-
- Dresden diamond, 171
-
- Drop-stone, 94
-
- Duke of Devonshire’s emerald, 191
-
-
- Edwardes ruby, 175
-
- Electrical characters, 82
-
- Emerald, 89, 184
- Brazilian, 220, 221
- Evening, 225
- Oriental, 111, 172
- Scientific, 122
- Uralian, 216
-
- Emeraldine, 247
-
- Emery, 175
-
- English Dresden diamond, 166
-
- Enstatite, 271
-
- Epidote, 275
-
- Essence d’Orient, 126
-
- Essonite (Hessonite), 211
-
- Euclase, 269
-
- Eugénie diamond, 164
-
- Evening emerald, 225
-
- Excelsior diamond, 167
-
- Extinction, 45
-
-
- Faceting machine, 105
-
- False topaz, 239
-
- Felspar, 254
-
- Fire, 20, 96
-
- Fire-marble, 289
-
- Fire-opal, 251
-
- Flats, 150
-
- Flêches d’amour, 240
-
- Flint, 247
-
- Floors, 147
-
- Fluor, 285
-
- Frémy, E., 115
-
-
- Garnet, 207
- Green, 271
-
- Gaudin, M. A. A., 115
-
- Gauges, Diamond, 86
-
- Girdle, 92
-
- Glass, 7, 124
-
- Gnaga Boh ruby, 180
-
- Goniometer, 30
-
- Grain, Pearl, 86
-
- Graphite, 129
-
- Greaser, 149
-
- Great Mogul diamond, 161
-
- Great Southern Cross group of pearls, 294
-
- Great Table diamond, 162
-
- Great White diamond, 167
-
- Green garnet, 271
-
- Greenstone, 261
-
- Grossular, 211
-
-
- Habit, 12
-
- Hardness, 78
-
- Haüynite, 286
-
- Heavy liquids, 64
-
- Hematite, 282
-
- Hessonite, 211
-
- Hexagonal system, 10
-
- Hiddenite, 266
-
- Hope cat’s-eye, 237
- chrysolite, 237
- diamond, 170
- pearl, 294
- sapphire, 121
-
- Hornstone, 247
-
- Hungarian cat’s-eye, 244
-
- Hyacinth, 211, 228
-
- Hydrophane, 250
-
- Hydrostatic weighing, 72
-
- Hypersthene, 271
-
-
- Iceland-spar, 40, 44
-
- Idocrase, 274
-
- Imitation stones, 124
-
- Imperial diamond, 167
-
- Index of refraction, 16
-
- India stones, 137, 181, 194, 215, 243, 244, 248, 290
-
- Indicators, 65
-
- Indicolite, 221
-
- Interference of light, 39, 48
-
- Iolite, 266
-
- Iris, 240
-
- Isle of Wight diamonds, 243
-
- Isomorphous replacement, 13, 19
-
-
- Jacinth, 211, 228
-
- Jade, 260
-
- Jadeite, 262
-
- Jargoon, 228
-
- Jasper, 247
-
- Jehan Ghir Shah diamond, 163
-
- Jigger, 149
-
- Jubilee diamond, 167
-
-
- Kauri-gum, 299
-
- Khiraj-i-Alam ruby, 206
-
- Kimberlite, 152
-
- King topaz, 181, 201
-
- Klein’s solution, 67
-
- Koh-i-nor diamond, 137, 158
-
- Kunz, Dr. G. F., 186, 224, 262, 265
-
- Kunzite, 265
-
- Kyanite, 79, 273
-
-
- Labradorite, 255
-
- La Pellegrina pearl, 294
-
- Lapis lazuli, 286
-
- Lazurite, 286
-
- Lozenge facet, 93
-
- Lumachelle, 289
-
- Lustre, 37
-
-
- Maacles, Macles, 12, 150
-
- Madagascar stones, 195, 224, 243, 265, 266
-
- Malachite, 287
-
- Malacolite, 272
-
- Manufactured stones, 113
-
- Marble, 289
-
- Mattan diamond, 155, 170
-
- Matura diamonds, 232
-
- Mazarin, Cardinal, 92
-
- Meerschaum, 288
-
- Mêlée, 136
-
- Methylene iodide, 26, 66
-
- Metric carat, 85, 87
-
- Milky-quartz, 240
-
- Minimum deviation, 30
-
- Mocha-stone, 247
-
- Moe’s gauge, 87
-
- Mohs’s scale of hardness, 78
-
- Moissan, Henri, 153
-
- Moldavite, 283
-
- Monoclinic system, 11
-
- Moon of the Mountains diamond, 162
-
- Moonstone, 39, 255
-
- Morganite, 186, 195
-
- Moroxite, 279
-
- Moss-agate, 247
-
- Mother-of-emerald, 240
-
- Mother-o’-pearl, 292
-
-
- Nacre, 292
-
- Napoleon diamond, 164
-
- Nassak diamond, 163
-
- Negative double refraction, 45
-
- Nephrite, 261
-
- Nicol’s prism, 44
-
- Nizam diamond, 162
-
-
- Obsidian, 283
-
- Occidental topaz, 111, 239
-
- Odontolite, 259
-
- Off-coloured diamonds, 130
-
- Olivine (demantoid), 216
- (peridot), 225
-
- Onyx, 247
-
- Opal, 39, 249
- Fire, 251
- -matrix, 251
-
- Opalescence, 39
-
- Optical anomalies, 47
-
- Optic axes, 49
-
- Oriental almandine, 112, 172
- amethyst, 111, 172
- emerald, 111, 172
- topaz, 111, 172
-
- Orient of pearls, 292
-
- Orloff diamond, 160
-
- Orthoclase, 254
-
- Orthorhombic system, 11
-
-
- Pacha of Egypt diamond, 165
-
- Paste, 47, 124
-
- Paul I diamond, 171
-
- Pavilion, 93
-
- Pavilion facet, 93
-
- Pear-drop pearls, 292
-
- Pear-eye pearls, 292
-
- Pearl, 291
- grain, 86
- imitations, 126
-
- Pendeloque, 94
-
- Peridot, 225
- Brazilian, 221
- Ceylonese, 221
-
- Peruzzi, Vincenzio, 92
-
- Phenakite, 269
-
- Pigott diamond, 164
-
- Pipes, 152
-
- Pistacite, 275
-
- Pitt diamond, 100, 159
-
- Plasma, 247, 264
-
- Pleochroism, 57
-
- Pleonaste, 204
-
- Pliny, 6, 88, 138, 184, 191, 241, 249
-
- Polar Star diamond, 163
-
- Polarization, 42
-
- Porter-Rhodes diamond, 166
-
- Positive double refraction, 45
-
- Prase, 240, 247
-
- Prehnite, 278
-
- Pycnometer, 75
-
- Pyrites, 282
-
- Pyrope, 212
-
-
- Quartz, 50, 238
-
- Quoin facet, 93
-
-
- Rainbow-quartz, 240
-
- Reconstructed stones, 116
-
- Reef, 144
-
- Reflection of light, 14
-
- Refraction of light, 15
-
- Refractive index, 16
-
- Refractometer, 22, 50
-
- Regent diamond, 100, 159
-
- Retgers’s salt, 69
-
- Rhodes, Cecil J., 145
-
- Rhodesia stones, 155, 183, 213, 236
-
- Rhodolite, 62, 214
-
- Rhodonite, 287
-
- Rock-crystal, 97, 239
-
- Rock-drill, 134
-
- Röntgen rays, 83
-
- Rose form of cutting, 91
-
- Rose-quartz, 240
-
- Rospoli sapphire, 182
-
- Rotation of plane of polarization, 50
-
- Rubellite, 220, 223
-
- Rubicelle, 203
-
- Ruby, 98, 110, 172
- Balas-, 203
- Cape-, 213
-
-
- Sancy diamond, 161
-
- Sapphire, 98, 110, 172
- Brazilian (tourmaline), 221
- -quartz, 244
- Water- (iolite), 266
- Water- (topaz), 201
-
- Sard, 247
-
- Sardonyx, 247
-
- Saussurite, 263
-
- Schorl, 221
-
- Scientific alexandrite, 122
- brilliant, 122
- emerald, 122
- topaz, 121
-
- Scotch topaz, 239
-
- Seed pearls, 294
-
- Serpentine, 289
-
- Setting of gem-stones, 107
-
- Shah diamond, 163
-
- Sheen, 39
-
- Shepherd’s Stone diamond, 163
-
- Siam stones, 180
-
- Siberia and Asiatic Russia stones, 182, 188, 194, 201, 217, 223,
- 236, 244, 256, 262, 269, 270, 287
-
- Siberite, 221
-
- Siderite, 244
-
- Silver-thallium nitrate, 69
-
- Skew facet, 93
-
- Skill facet, 93
-
- Smoky quartz, 240
-
- Snell’s laws, 16
-
- Soapstone, 288
-
- Sodalite, 286, 287
-
- Sonstadt’s solution, 67
-
- South Africa stones, 139 _et seq._, 166, 167 _et seq._, 213,
- 232, 244, 264, 271
-
- Spanish topaz, 239
-
- Specific gravity, 63
-
- Specific-gravity bottle, 75
-
- Spectroscope, 59
-
- Spectrum, 20, 25
-
- Spectrum, Absorption, 59
-
- Spessartite, 216
-
- Sphene, 276
-
- Spinel, 203
-
- Spodumene, 265
-
- Spotted stones, 149
-
- Star-facet, 92
-
- Star of Africa diamond, 168
-
- Star of Este diamond, 165
-
- Star of Minas diamond, 169
-
- Star of South Africa diamond, 141, 166
-
- Star of the South diamond, 139, 165
-
- Starstones, 38, 177
-
- Steatite, 288
-
- Step form of cutting, 98
-
- Stewart diamond, 166
-
- Strass, 124
-
- Sunstone, 255
-
- Synthetical stones, 113
-
- Syriam, Syrian, garnet, 215
-
-
- Table facet, 92
-
- Table form of cutting, 91
-
- Tavernier, J. B., 91, 129, 137, 161, 162, 170
-
- Templet facet, 92
-
- Tetragonal system, 9
-
- Thulite, 289
-
- Tiffany diamond, 171
-
- Tiger’s-eye, 39, 240
-
- Timur ruby, 206
-
- Titanite, 276
-
- Topaz, 197
- Brazilian, 197
- False, 239
- Occidental, 111, 239
- Oriental, 111, 173
- Scientific, 121
- Scotch, 239
- Spanish, 239
-
- Topazolite, 216
-
- Total-reflection, 18, 21
-
- Tourmaline, 43, 219
-
- Trap form of cutting, 98
-
- Trichroism, 57
-
- Triclinic system, 12
-
- Triplet, 126
-
- Turquoise, 257
-
- Turquoise-matrix, 258
-
- Tuscany diamond, 165
-
- Twinning, 12, 47
-
-
- Uniaxial double refraction, 45, 48 57
-
- Uralian emerald, 217
-
- Uvarovite, 218
-
-
- Variscite, 259
-
- Verdite, 264
-
- Verneuil, A. V. L., 116
-
- Vesuvianite, 274
-
- Victoria diamond, 167
-
- Violane, 287
-
-
- Wart-pearl, 296
-
- Water (of diamonds), 129
- (of pearls), 292
-
- Water-chrysolite, 284
- -sapphire (iolite), 266
- -sapphire (topaz), 201
-
- White opal, 249
-
- White Saxon diamond, 165
-
- Wollaston, W. H., 133
-
-
- X-rays, 83
-
-
- Yellow ground, 143
-
-
- Zircon, 228
-
-
- _Printed by_ MORRISON & GIBB LIMITED, _Edinburgh_
-
-
- +--------------------------------------------------------------------+
- | FOOTNOTES: |
- | |
- | [1] The word medium is employed by physicists to express any |
- | substance through which light passes, and includes solids such as |
- | glass, liquids such as water, and gases such as air; the nature |
- | of the substance is not postulated. |
- | |
- | [2] Methylene iodide must be heated almost to boiling-point to |
- | enable it to absorb sufficient sulphur; but caution must be |
- | exercised in the operation to prevent the liquid boiling over |
- | and catching fire, the resulting fumes being far from pleasant. |
- | It is advisable to verify by actual observation that the liquid |
- | is refractive enough not to show any shadow-edge in the field of |
- | view of the refractometer. |
- | |
- | [3] γωνία, angle; μέτρον, measure. For details of the |
- | construction, adjustment, and use of this instrument the reader |
- | should refer to textbooks of mineralogy or crystallography. |
- | |
- | [4] A cleavage flake of topaz may conveniently be used to show |
- | the phenomenon, but owing to the great width of the angle the |
- | “eyes” are invisible. |
- | |
- | [5] In accordance with the usual custom the angle between the |
- | facets is taken as that between their normals, or the supplement |
- | of the salient angle. |
- | |
- | [6] The word paste is derived from the Italian, _pasta_, food, |
- | being suggested by the soft plastic nature of the material used |
- | to imitate gems. |
- | |
- | [7] Cf. below, p. 149. |
- | |
- | [8] The least and the greatest of the refractive indices of |
- | doubly refractive species are given. |
- | |
- | [9] The dispersion is the difference of the refractive indices |
- | corresponding to the B and G lines of the solar spectrum. The |
- | value for crown-glass is ·016. |
- | |
- +--------------------------------------------------------------------+
-
-
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-End of the Project Gutenberg EBook of Gem-Stones and their Distinctive
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