Ore-forming processes of giant carbonate-hosted ZnPb deposit and Ge enrichment mechanism in Zhugongtang, Guizhou Province, China: Constraints from trace element and isotopic compositions of sulfides

IF 3.4 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Journal of Geochemical Exploration Pub Date : 2024-12-18 DOI:10.1016/j.gexplo.2024.107666
Qing Yang , Shao-Yong Jiang , Suo-Fei Xiong , Jun-Jie Hou
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Abstract

The Zhugongtang ZnPb deposit, with >3.27 million tons of Zn + Pb averaging 6.76 % Zn and 2.27 % Pb, along with 592 tons of Ge, is a newly discovered giant ZnPb deposit in northwest Guizhou Province of the Sichuan-Yunnan-Guizhou metallogenic region, Southwest China. This deposit is hosted in Devonian, Carboniferous, and Permian carbonate rocks. Three stages of hydrothermal mineralization were identified: (1) the pyrite-sphalerite-quartz stage, (2) the sphalerite-galena-pyrite-calcite stage, and (3) the carbonate stage, and three generations of sphalerite (Sp-1, Sp-2, and Sp-3) were identified. In this study, analyses of in situ trace element compositions in sphalerite and SPb isotopic compositions of sulfides were conducted to determine the origin and mineralization processes of the Zhugongtang deposit. Sphalerite is characterized by enrichment of Ge (mean = 109 ppm), Cd (mean = 875 ppm), and Ga (mean = 30 ppm) and depletion of In, Sn, and Co, with increasing Ge and Cu and decreasing Mn, Ag and Pb from the early to late stages. Ge incorporates into sphalerite via a coupled substitution of 3Cu+ + Sb3+ + Ge4+ ↔ 5Zn2+. The temperature and sulfur fugacity (fS2) are estimated from the trace element concentrations in sphalerite, which indicate medium- to low-temperature and intermediate-sulfidation conditions with decreasing temperature and fS2 from Sp-1 to Sp-3. The pyrite, sphalerite, and galena have δ34S values ranging from 11.3 to 17.8 ‰, 10.2 to 17.3 ‰, and 8.4 to 14.7 ‰, respectively, indicating that the reduced sulfur likely originated from the thermochemical reduction of sulfate (TSR) with multiple sources. High-precision in situ Pb isotope ratios of 208Pb/204Pb, 207Pb/204Pb, and 206Pb/204Pb range from 39.609 to 40.230, 15.860 to 16.042, and 18.768 to 18.984, respectively, which implies that the lead was sourced primarily from the host rock and basement strata. On the basis of a comprehensive analysis of ore geology and geochemical data, the Zhugongtang deposit is classified as an MVT deposit. With the gradual decrease in temperature and fS2, sphalerite (Sp-2 and Sp-3) precipitated in large quantities with significant enrichment of Ge (mean 147 ppm).

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来源期刊
Journal of Geochemical Exploration
Journal of Geochemical Exploration 地学-地球化学与地球物理
CiteScore
7.40
自引率
7.70%
发文量
148
审稿时长
8.1 months
期刊介绍: Journal of Geochemical Exploration is mostly dedicated to publication of original studies in exploration and environmental geochemistry and related topics. Contributions considered of prevalent interest for the journal include researches based on the application of innovative methods to: define the genesis and the evolution of mineral deposits including transfer of elements in large-scale mineralized areas. analyze complex systems at the boundaries between bio-geochemistry, metal transport and mineral accumulation. evaluate effects of historical mining activities on the surface environment. trace pollutant sources and define their fate and transport models in the near-surface and surface environments involving solid, fluid and aerial matrices. assess and quantify natural and technogenic radioactivity in the environment. determine geochemical anomalies and set baseline reference values using compositional data analysis, multivariate statistics and geo-spatial analysis. assess the impacts of anthropogenic contamination on ecosystems and human health at local and regional scale to prioritize and classify risks through deterministic and stochastic approaches. Papers dedicated to the presentation of newly developed methods in analytical geochemistry to be applied in the field or in laboratory are also within the topics of interest for the journal.
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