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 ?????, 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 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 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. 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 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. 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. 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 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. 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 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. 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 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, Fe2O3, by alumina, Al2O3, 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. |