The Corocoro copper deposits of Bolivia occur in beds of sandstone with no igneous rocks in the vicinity. However, they are all closely associated with a fault plane, igneous rocks occur at distances of a few miles, and the general mineralization is coextensive with the belt of igneous rocks; the deposits are therefore ascribed to a magmatic source rather than to sedimentary processes. Toward the surface the copper is in part in the form of sulphides, somewhat altered to oxide minerals, and farther down it is entirely native copper, associated with gypsum. This is the only district outside of Lake Superior where native copper has been mined on an important scale.
General comments. In general, the commercially prominent copper deposits show a close relationship to igneous rocks in place, time, and origin. Seldom do the ores extend more than 1,000 feet away from the igneous rock.
The common downward order in sulphide deposits is: first, a weathered zone, originally formed mainly above the water table, consisting above of a leached portion and below of oxides and carbonates of copper in a gangue of quartz or clay; second, a zone of secondary sulphide enrichment, characterized by chalcocite coatings, chalcopyrite, and pyrite, with a gangue of quartz and igneous rock or limestone; and third, a zone of primary deposition with similar gangue, characterized by chalcopyrite, and at Butte by enargite and chalcocite. The oxide zone as a whole may be rich or lean in values, depending on the nature of the associated gangue material and country rock. When these are more soluble than the copper—as is commonly the case in limestone—the copper may be residually concentrated, notwithstanding the fact that much copper originally present has been carried off in solution. When the associated gangue and country rock are less soluble than the copper—as is common with quartz and igneous rocks—the oxide zone is likely to be depleted of values.
The zones formed by weathering and secondary enrichment are extremely irregular, both in distribution and depth, in any one deposit, and they overlap and grade into one another in a very complex fashion. In many places the primary zone is too lean to be mined to commercial advantage; but in other places, as at Butte, and in the limestone deposits of Bingham, the primary ores are of considerable importance.
When evidence of secondary sulphide enrichment was first recognized there was a tendency to magnify its effectiveness, and to assume that in most cases the values were due to this process; that the primary zones would be found to be valueless. In recent years the emphasis is being somewhat changed because of the recognizing in many camps of rich primary zones. While some chalcocite is clearly the result of secondary enrichment from above, other chalcocite seems to have been related closely to the primary deposition. The quantitative discrimination of the two is a matter of great difficulty.
It has come to be recognized that the zonal arrangement caused by enrichment from the surface has been imposed usually on a zonal arrangement caused by the primary hot solutions and not related to the surface but to the source of the solutions. In some districts, as illustrated by Butte and Bingham, the copper-bearing minerals seem to have been deposited nearest the igneous source, while the lead, zinc, gold, and silver minerals have been deposited farther away,—suggesting the cooling of the solutions with increasing distance from the igneous source. The further investigation of this primary zonal arrangement promises interesting results with a practical bearing on exploration and development.
One of the newer features of the investigation of copper deposits has been the recognition of the cyclic nature of the secondary concentration. This process has been related not only to the present erosion surface, but to older surfaces now partly buried under later rocks. Ransome's[33] summary of conditions at the Ray-Miami camp has a somewhat general application.
Supergene enrichment has generally been treated as a continuously progressive process. There is considerable probability, however, that it is essentially cyclic, although the cyclic character may not be patent in all deposits. A full development of the cycle can take place only under a certain equilibrium of a number of factors, including climate, erosion, topography, and character of rock. The essential fact appears to be that as enrichment progresses and chalcocite increases the process of enrichment becomes slower in action, and erosion may, in some circumstances, overtake it. With the removal of some of the protecting zone of chalcocite the protore is again exposed to oxidation and a second cycle of enrichment begins.
Although much of the enriched ore is now below ground-water level, it probably was once above that level, and enrichment is believed to have taken place mainly in the zone of rock above any general water table.
Where the old erosion surface roughly coincides with the present erosion surface, the deposits follow more or less the topography. Where the old erosion surface pitches below later sediments, the ores pitch with it, and therefore do not follow the present topography. The recognition of the cyclic nature of secondary concentration is obviously of great significance in exploration and development.