Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-26T10:50:51.511Z Has data issue: false hasContentIssue false

Clay Alteration in Copper Deposits Associated with Granodiorites

Published online by Cambridge University Press:  01 January 2024

Charles Meyer*
Affiliation:
University of California, USA
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Recent development at deep levels in the Mt. Con Mine at Butte, Montana, has revealed a structurally early alteration type characterized by K-rich alkali feldspar, brown and green biotite, and 2M muscovite (sericite). This is similar to the K-rich biotite assemblage in numerous porphyry coppers as emphasized by Anderson, Gilluly, Creasey, and Rose. In Butte, and in some of the porphyry coppers, the assemblage is demonstrably earlier than the common feldspar-free, muscovite-quartz-pyrite assemblage which envelops pyrite-rich veinlets. On the other hand, few consistent mineral assemblages or detailed distribution patterns have yet emerged for argillic alteration, where illite, kaolinite, montmorillonite, and locally allophane and pyrophyllite are prominent phases. Probably much of the confusion results from extensive supergene alteration, though even this cannot be proved at present.

In supergene and in hypogene alteration at least below 300°C, supersaturation of SiO2 in the aqueous phase may play an important role in determining alteration assemblages. Some reactions affected ar. (1) the hydrolysis of K-spar to K-mica. (2) albite to montmorillonite. (3) silica-rich illite or montmorillonite to kaolinite, an. (4) pyrophyllite to kaolinite.

The encroachment of the sericitic zone on the argillic zone at Butte may be controlled by changes in ionic species of the veinward migrating SiO2 liberated by argillization of plagioclase. Within the sericitic zone and the veins, silica in solution is probably in equilibrium with quartz.

Type
Symposium on Mechanism of Emplacement (Formation) of Clay Minerals
Copyright
Copyright © The Clay Minerals Society 1963