Assuming, then, that gold originally existed as a mineral salt, when and how did it take metallic form? Doubtless, just in the same manner as we now (by means of well-known reagents which are common in nature) precipitate it in the laboratory. With regard to that found in quartz lodes finely disseminated through the gangue, the change was brought about by the same agency which caused the silicic acid to solidify and take the form in which we now see it in the quartz veins. Silica is soluble in solutions of alkaline carbonates, as shown in New Zealand geysers; the solvent action being increased by heat and pressure, so also would be the silicate or sulphide of gold. When, however, the waters with their contents were released from internal pressure and began to lose their heat the gold would be precipitated together with the salts of some other metals, and would, where the waters could percolate, begin to accretionise, thus forming the heavy or specimen gold of some reefs. On this class of deposition I shall have more to say when treating of the origin of alluvial gold in the form of nuggets. Mr. G. F. Becker, of the United States Geological Survey, writing of the geology of the Comstock lode, says:--“Baron Von Richthofen was of opinion that fluorine and chlorine had played a large part in the ore deposition in the Comstock, and this the writer is not disposed to deny; but, on the other hand, it is plain that most of the phenomena are sufficiently accounted for on the supposition that the agents have been merely solutions of carbonic and hydrosulphuric acids. These reagents will attack the bisilicates and felspars. The result would be carbonates and sulphides of metals, earths, alkalies, and free quartz, but quartz and sulphides of the metals are soluble in solutions of carbonates and sulphides of the earths and alkalies, and the essential constituents of the ore might, therefore, readily be conveyed to openings in the vein where they would have been deposited on relief of pressure and diminution of temperature. An advance boring on the 3000 ft. level of the Yellow Jacket struck a powerful stream of water at 3065 ft. (in the west country), which was heavily charged with hydrogen sulphide, and had a temperature of 170° F., and there is equal evidence of the presence of carbonic acid in the water of the lower levels. A spring on the 2700 ft. level of the Yellow Jacket which showed a temperature of about 150° F., was found to be depositing a sinter largely composed of carbonates.”