1. Trace Elements and Sulfur Isotopes of Sulfides in the Zhangquanzhuang Gold Deposit, Hebei Province, China: Implications for Physicochemical Conditions and Mineral Deposition Mechanisms.
- Author
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Zhen, Shimin, Wang, Dazhao, Yu, Xiaofei, Wang, Qingfei, Li, Yongsheng, Zha, Zhongjian, and Wang, Jiang
- Subjects
SULFUR isotopes ,GOLD ,SILVER sulfide ,TRACE elements ,MINERALS ,TELLURIDES ,SULFIDES - Abstract
The Zhangquanzhuang gold deposit is a special deposit in the Zhangjiakou district, on the northern margin of the North China Craton. It is characterized by the enrichment of sulfides, the scarcity of tellurides and zero to positive sulfur isotope compositions compared with the famous Dongping and Xiaoyingpan Te-Au-Ag deposit types of the same district. In this paper, we use the in-situ LA-(MC)-ICP-MS and bulk trace element concentrations of pyrite, and in-situ sulfur isotope compositions of sulfides, to study physicochemical conditions and mechanisms of mineral deposition in the Zhangquanzhuang deposit. Pyrite from stage I (PyI) contains high Te contents, pyrite from stage II (PyII) has the highest Co and Ni contents, and pyrite from stage III (PyIII) contains high Cr, Zn, Pb, Ag, Cu, Sb, Bi and Au contents. The calculated in-situ δ
34 SH2S values range from 0.9‰ to 6.1‰, and the values for stages I and II are higher than those for stage III. The mineral assemblages and trace element contents in pyrite show that large amounts of metals precipitated during stage III, in which the pH and logfO2 were constrained within the range of 4.1 to 5.2 and −36.9 to −32.1, respectively. Sulfidation and boiling derived from decreasing pressure may be the main mechanisms leading to mineral deposition in stage III. The Zhangquanzhuang gold deposit was formed in a mineral system that was different from the one that formed the Dongping and Xiaoyingpan Te-Au-Ag deposits, and should thus be called the "Zhangquanzhuang−type" deposit and considered a third gold deposit type in the Zhangjiakou ore field. [ABSTRACT FROM AUTHOR]- Published
- 2020
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