Ore genesis of the Fule Pb-Zn deposit and its relationship with the Emeishan Large Igneous Province: Evidence from mineralogy, bulk C-O-S and in situ S-Pb isotopes

被引:74
作者
Zhou, Jia-Xi [1 ,3 ,6 ]
Luo, Kai [1 ,2 ]
Wang, Xuan-Ce [3 ]
Wilde, Simon A. [3 ]
Wu, Tao [4 ,6 ]
Huang, Zhi-Long [1 ]
Cui, Yin-Liang [5 ]
Zhao, Jian-Xin [6 ]
机构
[1] Chinese Acad Sci, Inst Geochem, Stake Key Lab Ore Deposit Geochem, Guiyang 550081, Guizhou, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Curtin Univ, Inst Geosci Res, Dept Appl Geol, GPO Box U7987, Perth, WA 6845, Australia
[4] Zhejiang Univ, Sch Earth Sci, Hangzhou 310027, Zhejiang, Peoples R China
[5] Yunnan Nonferrous Met Geol Bur, Kunming 650051, Yunnan, Peoples R China
[6] Univ Queensland, Sch Earth & Environm Sci, Radiogen Isotope Facil, Brisbane, Qld 4072, Australia
基金
中国国家自然科学基金;
关键词
NanoSIMS in situ S isotopes; Fs LA-MC-ICPMS in situ Pb isotopes; Role of Emeishan magmatism; Carbonate-hosted Pb-Zn deposits in the ELIP; South China; THERMOCHEMICAL SULFATE REDUCTION; LEAD-ZINC DEPOSITS; SOUTHWEST CHINA; YUNNAN PROVINCE; GUIZHOU PROVINCE; SULFIDE MINERALS; FLOOD-BASALTS; HYDROTHERMAL CALCITE; NORTHEASTERN YUNNAN; INDOSINIAN OROGENY;
D O I
10.1016/j.gr.2017.11.004
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Magmatic activity plays an important role in mineralization, but little is understood of its role with respect to carbonate-hosted stratabound epigenetic Pb-Zn deposits. The Fule Pb-Zn deposit (similar to 10 Mt of sulfide ore with mean grades of 15-20 wt% Zn + Pb), is stratigraphically placed in middle Permian strata and spatially (similar to 1 m) associated with late Permian continental flood basalts of the Emeishan Large Igneous Province (ELIP). It thus provides an ideal case to investigate its genetic relationship with the ELIP. In addition, the Fule deposit is characterized by high concentrations of Ag, Cd, Ge and Ga, and contains a variety of Cu and Ni sulfide minerals. Syn-ore calcite (delta C-13 = +2.57-+ 3.01 parts per thousand) and associated fluids (delta C-13 = +2.96-+ 3.40 parts per thousand) have delta C-13 values similar to those of fresh limestone (delta C-13 = +1.58-+ 2.63 parts per thousand), but the delta O-18 values of calcite (+16.83-+ 19.92 parts per thousand) and associated fluids (+7.80-+ 10.89 parts per thousand) are distinctly lower than those of limestone (delta O-18 = +21.85-+23.61 parts per thousand). This means that C is mainly derived from limestone, whereas the O isotope signature may be related to water/rock (W/R) interaction between mantle and/or metamorphic fluids and limestone. delta S-34 values of sulfide minerals obtained by in situ NanoSIMS and conventional bulk techniques record a range of +9.8- +23.1 parts per thousand and +10.04-+ 16.43 parts per thousand, respectively, reflecting the enrichment of heavy S isotopes in the ore-forming fluids and ther-mochemical sulfate reduction (TSR) is the principal mechanism for the formation of S2-. Cores of sulfide crystals have much higher delta S-34 values than their rims, indicating a probable mixture of multiple S reservoirs and/or a dynamic fractionation of S isotopes occurred during sulfide precipitation. The uniform femtosecond (fs) LA-MC-ICPMS in situ Pb isotopic data for galena plot in the field that differs from any of the three potential sources in the region. Such signatures demonstrate that metal Pb was most likely derived from a well-mixed source of basalts, sedimentary rocks and basement rocks. We propose that (a) the enrichment in Ag, Cu, Ni, Cd, Ge and Ga, and the isotope signatures of hydrothermal minerals in the Fule region are related to fluids derived from or flowed through multiple reservoirs; (b) Emeishan magmatism provided heat, elements and associated fluids, and its basalts acted as an impermeable and protective layer; and (c) fluid mixing caused TSR, and then resulted in W/R interaction and CO2 degassing, all of which played a key role in the precipitation of hydrothermal minerals. (C) 2017 International Association for Gondwana Research. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 179
页数:19
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