中国长江下游金属成矿带独特的姚家岭锌-金-铜矿床硫化物的硫同位素和微量元素地球化学:对成矿过程和勘探的影响

IF 3.4 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Yu Wang , Xiaoyong Yang , Xuanyang Feng , Huishan Zhang , Shasha Liu , Fangyue Wang
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引用次数: 0

摘要

姚家岭锌-铜-铜矿床是斑岩-矽卡岩-热液脉型复合矿床,由热液脉型铅锌银矿体、矽卡岩型锌-铜-金矿体、斑岩型铜-金矿体由浅到深组成。我们通过研究三种矿体中硫化物(黄铁矿、闪锌矿、黄铜矿和方铅矿)的微量元素和 S 同位素组成,破译了其来源和成矿机制。采集到的黄铁矿可分为两种类型。黄铁矿与黄铜矿共生,黄铁矿与闪锌矿或方铅矿共生。此外,PyI 又分为 PyIa(从斑岩铜矿体中采集)和 PyIb(从矽卡岩铜矿体中采集)。PyII又可分为PyIIa(采集自矽卡岩型铅锌矿体)和PyIIb(采集自地层中的脉状铅锌矿体)。黄铁矿和闪锌矿微量元素温度计显示,成矿流体的温度从斑岩矿体的 500 ℃至 600 ℃下降到矽卡岩矿体的 300 ℃至 360 ℃,再下降到浅部脉岩矿体的 240 ℃至 280 ℃。从深部到浅部采集到的黄铁矿中 Co 和 Ni 含量的下降可能表明,成矿热液系统后期析出了陨石水。流体的快速结晶和物理化学状态(如温度、pH值、fO2和地球化学成分)的变化,导致八面体黄铁矿颗粒形成明显的振荡带。这也影响了微量金属元素的溶解度,并导致这些元素选择性地进入黄铁矿。PyII 也表现出明显的分带特征,而不是振荡分带,这表明黄铁矿的生长速度相对较慢。此外,两种黄铁矿中金和砷含量的关系也不同。PyI 是耦合的,而 PyII 则是解耦的。我们认为,这种现象是由于成矿流体体系中 As 含量较高,可能会抑制黄铁矿表面对 Au 的吸收,而不是由于 PyII 中 As 含量的快速增加和非振荡分带造成的 Au 和 As 的解耦。根据各种硫化物的硫同位素分析,固体证据表明姚家岭矿床各类矿体的成矿物质主要来源于岩浆-热液过程,硫同位素的分馏是岩浆-热液演化引起的物理化学条件变化的结果,而不是外来硫源加入的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sulfur isotope and trace element geochemistry of sulfides from the unique Yaojialing Zn-Au-Cu deposit, Lower Yangtze River Metallogenic Belt, China: Implications for ore-forming process and exploration

Sulfur isotope and trace element geochemistry of sulfides from the unique Yaojialing Zn-Au-Cu deposit, Lower Yangtze River Metallogenic Belt, China: Implications for ore-forming process and exploration

The Yaojialing Zn-Au‑Cu deposit is a porphyry-skarn-epithermal vein-type compound deposit that consists of epithermal vein-type lead‑zinc‑silver orebodies, skarn Zn-Cu-Au orebodies, and porphyry CuAu orebodies from shallow level to depth. We decipher the source and metallogenic mechanism by studying the trace element and S isotopic compositions of sulfides (pyrite, sphalerite, chalcopyrite, and galena) from three types of orebodies. The collected pyrite can be divided into two types. PyI coexists with chalcopyrite, and PyII coexists with sphalerite or galena. In addition, PyI was further divided into PyIa (collected from porphyry copper bodies) and PyIb (collected from skarn copper bodies). PyII can be further divided into PyIIa (collected from skarn-type lead‑zinc ore body) and PyIIb (collected from vein lead‑zinc ore body in strata). Sphalerite and galena from skarn-type PbZn ore bodies and shallow vein-type PbZn ore bodies are named SpI and GnI, and SpII and GnII, respectively.

Pyrite and sphalerite trace element thermometers revealed that the temperature of the ore-forming fluids decreased from 500 to 600 °C in the porphyry ore body to 300– 360 °C in the skarn ore body and then to 240– 280 °C in the shallow vein ore body. The decrease in the Co and Ni contents of pyrite collected from deep to shallow depths may indicate that meteoric water precipitated in the late ore-forming hydrothermal system. Rapid crystallization and variations in the physicochemical states (such as temperature, pH, fO2, and geochemical composition) of the fluids resulted in an obvious oscillating zone of euhedral PyI pyrite particles. It also affects the solubility of trace metal elements and leads to the selective entry of these elements into pyrite. PyII also shows obvious zonation characteristics rather than oscillating zonation, indicating that the growth rate of pyrite is relatively slow. Moreover, the relationships between the Au and As contents in the two types of pyrite are different. PyI is coupled, while PyII shows decoupling. We believe that this phenomenon is due to the high content of As in ore-forming fluid systems, which may inhibit the absorption of Au on the surface of pyrite rather than the decoupling of Au and As caused by rapid crystallization, based on the rapid increase in As content and non-oscillating zonation in PyII. According to the analysis of the sulfur isotopes of various sulfides, the solid evidences suggest that the ore-forming materials of each type of orebody in the Yaojialing deposit were mainly derived from magmatic-hydrothermal processes and that the fractionation of sulfur isotopes was the result of variations in physicochemical conditions caused by magma-hydrothermal evolution rather than the addition of foreign sulfur sources.

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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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