The mineral topaz is found in Cornwall and in the British Isles generally; also in Siberia, India, South America and many other localities, some of the finest stones coming from Saxony, Bohemia, and Brazil, especially the last-named. The cleavage is perfect and parallel to the basal plane. It crystallises in the 4th (rhombic) system; in lustre it is vitreous; it is transparent, or ranging from that to translucent; the streak is white or colourless.

Its colour varies very much -some stones are straw-colour, some are grey, white, blue, green, and orange. A very favourite colour is the pink, but in most cases this colour is not natural to the stone, but is the result of “burning,” or “pinking” as the process is called technically, which process is to raise the temperature of a yellow stone till the yellow tint turns to a pink of the colour desired.

The topaz is harder than quartz, as will be seen on reference to the “Hardness” table, and is composed of a silicate of aluminium, fluorine taking the place of some of the oxygen. Its composition averages 16.25 per cent. of silica, 55.75 per cent. of alumina, or oxide of aluminium, and fluoride of silicium, 28 per cent. Its formula is [Al(F,OH)]2 SiO4, or (AlF)2SiO4.

From this it will be understood that the fluorine will be evolved when the stone is fused. It is, however, very difficult to fuse, and alone it is infusible under the blowpipe, but with microcosmic salt it fuses and evolves fluorine, and the glass of the tube in the open end of which the stone is fixed is bitten with the gas.

Such experiments with the topaz are highly interesting, and if we take a little of the powdered stone and mix with it a small portion of the microcosmic salt, we may apply the usual test for analysing and proving aluminium, thus: a strongly brilliant mass is seen when hot, and if we moisten the powder with nitrate of cobalt and heat again, this time in the inner flame, the mass becomes blue.

Other phenomena are seen during the influence of heat. Some stones, as stated, become pink on heating, but if the heating is continued too long, or too strongly, the stone is decoloured.

Others, again, suffer no change, and this has led to a slight difference of opinion amongst chemists as to whether the colour is due to inorganic or organic matter. Heating also produces electricity, and the stone, and even splinters of it, will give out a curious phosphorescent light, which is sometimes yellow, sometimes blue, or green. Friction or pressure produces strong electrification; thus the stones may be electrified by shaking a few together in a bag, or by the tumbling of the powdered stone-grains over each other as they roll down a short inclined plane. The stones are usually found in the primitive rocks, varying somewhat in different localities in their colour; many of the Brazilian stones, when cut as diamonds, are not unlike them.

In testing, besides those qualities already enumerated, the crystalline structure is specially perfect and unmistakable. It is doubly refractive, whereas spinel and the diamond, which two it closely resembles, are singly refractive. Topaz is readily electrified, and, if perfect at terminals, becomes polarised; also the commercial solution of violets, of which a drop only need be taken for test, is turned green by adding to it a few grains of topaz dust, or of a little splinter crushed to fine powder.

In the ordinary varieties this is somewhat poor, being mostly blue, or a dirty or a greenish yellow; the better kinds, however, possess magnificent colour and variety, such as in the aquamarine, emerald, etc.

The cleavage is parallel to the basal plane. Its lustre is sometimes resinous, sometimes vitreous, and it crystallises in the 2nd (hexagonal) system. It occurs in somewhat long, hexagonal prisms, with smooth, truncated planes, and is often found in granite and the silt brought down by rivers from granite, gneiss, and similar rocks.

It is found in Great Britain and in many parts of Europe, Asia, and America, in crystals of all sizes, from small to the weight of several tons. The common kinds are too opaque and colourless to be used as gems and are somewhat difficult of fusion under the blowpipe, on the application of which heat some stones lose their colour altogether, others partly; others, which before heating were somewhat transparent, become clouded and opaque; others suffer no change in colour, whilst some are improved. In almost every case a slight fusion is seen on the sharp edges of fractures, which become smooth, lose their sharpness, and have the appearance of partly fused glass.

The hardness varies from 7-1/4 to 8, the crystals being very brittle, breaking with a fracture of great unevenness. The better varieties are transparent, varying from that to translucent, and are called the “noble” beryls. Transparent beryl crystals are used by fortune-tellers as “gazing stones,” in which they claim to see visions of future events.

In colour it is blue or greenish-blue, sometimes opaque, varying between that and feeble translucency, though it should be said that in all forms, even those considered opaque, a thin cutting of the stone appears almost transparent, so that the usual classing of it among the opaque stones must be done with this reservation.

In composition it contains about 20 per cent. of water, about a third of its substance being phosphoric acid, or phosphorus-pentoxide; sometimes nearly half of it is alumina, with small quantities of iron in the form of variously coloured oxides, with oxide of manganese.

The great proportion of water, which it seems to take up during formation, is mostly obtained in the cavities of weathered and moisture-decomposing rocks. Its average formula may be said to be Al2O3P2O5 + 5H2O, and sometimes Al2O3 FeOP2O5 + 5H2O.

It must therefore follow that when the stone is heated, this water will separate and be given off in steam, which is found to be the case. The water comes off rapidly, the colour of the stone altering meanwhile from its blue or blue-green to brown. If the heat is continued sufficiently long, this brown will deepen to black, while the flame is turned green. This is one of the tests for turquoise, but as the stone is destroyed in the process, the experiment should be made on a splinter from it.

This stone is of very ancient origin, and many old turquoise deposits, now empty, have been discovered in various places. History records a magnificent turquoise being offered in Russia for about £800 a few centuries ago, which is a very high price for these comparatively common stones.

Owing to the presence of phosphorus in bones, it is not uncommon to find, in certain caves which have been the resort of wild animals, or into which animals have fallen, that bones in time become subjected to the oozing and moisture of their surroundings; alumina, as well as the oxides of copper, manganese and iron, are often washed across and over these bones lying on the cave floor, so that in time, this silt acts on the substance of the bones, forming a variety of turquoise of exactly the same composition as that just described, and of the same colour.

So that around the bones there eventually appears a beautiful turquoise casing; the bone centre is also coloured like its casing, though not entirely losing its bony characteristics, so that it really forms a kind of ossified turquoise, surrounded by real turquoise, and this is called the “bone turquoise” or “odontolite.”