Scheelite of the Bystrinskoe Skarn-Porphyry Cu–Au–Fe Deposit, Eastern Transbaikal Region, Russia: Genetic Implications

白钨矿 矽卡岩 矿化(土壤科学) 地质学 地球化学 辉钼矿 矿物 矿物学 阴极发光 黑钨矿 斑岩铜矿 电子探针 石英 硫化物 流体包裹体 化学 材料科学 有机化学 土壤水分 土壤科学 古生物学 光电子学 发光
作者
В. А. Коваленкер,O. Yu. Plotinskaya,G. D. Kiseleva,E. A. Minervina,С. Е. Борисовский,О. М. Zhilicheva,Yu. I. Yazykova
出处
期刊:Geology of Ore Deposits [Pleiades Publishing]
卷期号:61 (6): 559-579 被引量:8
标识
DOI:10.1134/s1075701519060035
摘要

The first results of optical microscopy, cathodoluminescence (CL), ultraviolet fluorescence (UV), electron-probe microanalysis (EPMA), and laser-ablation inductively-coupled plasma-mass spectrometry (LA-ICPMS) study of scheelite from quartz–molybdenite and quartz–carbonate–sulfide veins and veinlets (porphyry type), as well as the magnetite–sulfide massive, veinlets, and disseminated (skarn type) associations, of the Bystrinskoe skarn-porphyry Cu–Au–Fe deposit in the Eastern Transbaikal region, one of the largest gold–copper porphyry deposits in Russia, are reported. Despite the fact that scheelite is not a major ore mineral, it is found almost everywhere. This makes it possible to identify its crucial genetic features in both the two types of mineralization and the deposit as a whole. It is shown that scheelite from different types of mineralization has clearly determined individual characteristics, differing in abundance, associated minerals, CL and UV color, composition and concentrations of major and trace elements, and REE distribution patterns. These crucial features testify to a significant difference in the formation conditions of the studied mineralization types and reveal the dependence on the physicochemical and compositional parameters of the mineral-forming environment. This allows one to consider scheelite as a fundamentally important genetic indicator of the mineral-forming environments' evolution. Crucially important are the molybdenum concentration in scheelite and the type and shape of REE-spectra, which are generally controlled by mineral-forming fluid chemistry, the incorporation of REE in the structure of the mineral, and variations in the redox properties of the mineral-forming fluid.
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