喀尔巴阡山脉中西部塔特拉山脉波兰部分的热液矿化

IF 0.4 Q4 ENVIRONMENTAL SCIENCES
Magdalena Sitarz, B. Gołębiowska, K. Nejbert, D. Dimitrova, R. Milovský
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引用次数: 2

摘要

在西塔特拉山脉的波兰部分有几个热液矿化区。块状和浸染的硫化物,主要是来自四面体群和黄铜矿的矿物,填满石英脉,伴随着菱铁矿、白云石和重晶石,其中许多是在16至18世纪之间开采的。本文介绍了常见硫化物的矿物学资料,并对四面体中硫的同位素组成和热液流体的成因进行了初步研究。矿石中最常见的原生硫化物矿物为四面体-(Zn)和四面体-(Fe),对应的Zn范围为1.83 ~ 5.87 wt.% (0.47 ~ 1.44 apfu), Fe范围为1.63 ~ 5.05 wt.% (0.48 ~ 1.52 apfu)。用As代替Sb,砷含量最高可达7.25 wt.% (1.588 apfu), Sb/(Sb+As) = 0.60。2个品种的Bi和Hg含量分别上升0.6 wt.% (0.049 apfu)和0.96 wt.% (0.081 apfu);976 ppm), Cd(最大;735 ppm), In(最大;14 ppm)。黄铜矿、黄铁矿和方铅矿的组成接近理想公式。所研究的四面体和黄铜矿中微量元素含量的差异可以用元素分配来解释。矿石中铟、镓、锡的分布特征表明成矿作用形成于低温低压条件下。石英原生包裹体均一温度在120 ~ 174℃范围内,表明成矿源处于低温阶段,来自低矿化度流体(高达17.92 wt.% NaCl eq)。四面体群矿物的稳定δ34S同位素表明,火成岩流体可能是矿石结晶的来源之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrothermal ore mineralization from the Polish part of the Tatra Mts., Central Western Carpathians
Several areas with hydrothermal ore mineralization are present in the Polish part of the Western Tatra Mts. Massive and disseminated sulfides, mainly minerals from the tetrahedrite group and chalcopyrite, fill quartz veins accompanied by siderite, dolomite and baryte – many of these were mined between the 16th and 18th century. This paper presents information on the mineralogy of the common sulfides and the preliminary studies of both the isotopic composition of sulfur in tetrahedrite as well as the origin of hydrothermal fluids. The most common primary sulfide minerals in the ores are tetrahedrite-(Zn) and tetrahedrite-(Fe) corresponding to Zn ranges from 1.83 to 5.87 wt.% (0.47–1.44 apfu), and Fe from 1.63 to 5.05 wt.% (0.48–1.52 apfu). The substitution of As for Sb shows maximum As content of 7.25 wt.% (1.588 apfu) which corresponds to the Sb/(Sb+As) = 0.60. Both varieties show substitutions of Bi and Hg, up 0.6 wt.% (0.049 apfu) and 0.96 wt.% (0.081 apfu), respectively, and content of trace elements: Co (max. 976 ppm), Cd (max. 735 ppm), In (max. 14 ppm). Chalcopyrite, pyrite, and galena show compositions close to the ideal formula. Differences in the content of trace elements in the studied tetrahedrite and chalcopyrite were explained by element partitioning between these minerals. The distributions of In, Ga and Sn in the studied minerals indicate that the mineralization was formed at low temperature and pressure. The homogenization temperature of the primary inclusions in quartz in the range of 120–174°C indicate the origin of mineralization in low-temperature stage from low salinity fluids (up to 17.92 wt.% NaCl eq.). Stable δ34S isotopes in minerals of the tetrahedrite group suggest that the igneous fluids might be one of the sources from which ores were crystallized.
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