用户名: 密码: 验证码:
Brines related to Ag deposition in the Zgo
详细信息      PDF全文下载
摘要

The Zgounder ores occur in sets of quartz-calcite veinlets, cross-cutting the Middle-Precambrian volcanosedimentary formations of Sirwa (Anti-Atlas, Morocco). Two major stages of mineralization are distinguished: i) A first stage is characterized by the deposition of quartz (biotite) together with As-Co minerals. This stage is also characterized by a variety of H 2 O-CO 2 -CH 4 fluids with moderate densities, interpreted as fluids equilibrated with metasediments. These fluids are trapped under rather high temperatures (around 400-450 degrees C) and a rather wide range of pressures attesting to probable pressure fluctuations from hydrostatic to lithostatic conditions. In addition to pressure and temperature drops, aqueous-carbonic fluids have probably undergone episodic immiscibility, the latter process likely being related to the deposition of metals. ii) The second stage corresponds to the major (Cu-Zn)-Ag(Hg) ore deposition and clearly postdates the As-Co assemblage. Silver deposition occurs after the crystallization of quartz-sphalerite-chalcopyrite veins, but both Cu-Zn and Ag(Hg) ore-bearing fluids are NaCl-CaCl 2 brines (24 to 40 wt.% eq. NaCl + CaCl 2 ). Brines occur as several fluid inclusion types (L+V+ or -halite cube), and were trapped under minimum temperatures of around 160-200 degrees C. The ion chemistry of the fluid inclusions determined by crush-leach analysis shows that brines display typical features of sedimentary fluids which interacted with evaporites: Na/K ratio ranges from 10 to 12, Na/Ca from 1.9 to 2.4, Na/Li from 220 to 445, Cl/Br from 300 to 380 and Cl/SO 4 from 1100 to 2100. Fluids at the origin of the Zgounder Ag mineralization are thus Na-Ca brines unrelated to the earlier As-Co ores. Dilution and slight cooling are the two main driving mechanisms for silver deposition, as in several other examples from Anti-Atlas or Canada.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700