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赞比亚铜带省谦比希铜矿床成因:来自流体包裹体和H-O-S同位素地球化学证据
引用本文:胡乔帆,冯佐海,莫江平,方科,刘俊辰,蔡永丰,邓贵安,黄学强,白令安,覃鹏.赞比亚铜带省谦比希铜矿床成因:来自流体包裹体和H-O-S同位素地球化学证据[J].地球科学,2021,46(5):1554-1568.
作者姓名:胡乔帆  冯佐海  莫江平  方科  刘俊辰  蔡永丰  邓贵安  黄学强  白令安  覃鹏
作者单位:桂林理工大学广西隐伏金属矿产勘查重点实验室,广西桂林 541004;中国有色桂林矿产地质研究院有限公司,广西桂林 541004;桂林理工大学广西隐伏金属矿产勘查重点实验室,广西桂林 541004;中国有色桂林矿产地质研究院有限公司,广西桂林 541004;中国地质科学院矿产资源研究所,自然资源部成矿作用与资源评价重点实验室,北京 100037
基金项目:国家自然科学基金项目41572191国家自然科学基金项目41762007广西自然科学基金项目2017GXNSFBA198203广西自然科学基金项目2018GXNSFBA281069广西自然科学基金项目2019GXNSFDA245009广西隐伏金属矿产勘查重点实验室开放课题资助项目20-065-17-K02
摘    要:为揭示谦比希铜矿床的成矿流体性质、成矿物质来源及其演化特征,对其矿石和脉石矿物展开了流体包裹体和H-O-S同位素地球化学研究.结果显示,热液型脉状矿化石英流体包裹体均一温度变化于100~350 ℃,盐度变化于11%~19%NaCleqv;δDV-SMOW值为-64.0‰~-52.6‰,δ18OH2O值为1.57‰~2.97‰.热液型脉状和沉积型层状铜矿体δ34SCDT值分别变化于5.5‰~12.1‰和6.0‰~21.0‰.分析表明,热液型成矿流体属Cl-Na-Ca型水溶液,属中低密度流体;成矿流体受幔源和壳源岩浆混合,导致铜发生沉淀.沉积型层状矿化硫主要来自成岩硫化物和海水硫酸盐,硫酸盐以热化学还原为主,导致SO42-较彻底的变为H2S.整体看来,谦比希铜矿床热液型脉状矿化与新元古代中期岩浆活动密切相关,沉积型层状矿化主要与新元古代晚期大规模造山运动和区域变质作用有关. 

关 键 词:流体包裹体  H-O-S同位素  成矿流体  谦比希铜矿床  赞比亚  矿床学
收稿时间:2020-11-23

Genesis of Chambishi Copper Deposit in Copperbelt Province of Zambia:Evidence from Fluid Inclusions and H-O-S Isotope Geochemisty
Hu Qiaofan,Feng Zuohai,Mo Jiangping,Fang Ke,Liu Junchen,Cai Yongfeng,Deng Gui?an,Huang Xueqiang,Bai Ling?an,Qin Peng.Genesis of Chambishi Copper Deposit in Copperbelt Province of Zambia:Evidence from Fluid Inclusions and H-O-S Isotope Geochemisty[J].Earth Science-Journal of China University of Geosciences,2021,46(5):1554-1568.
Authors:Hu Qiaofan  Feng Zuohai  Mo Jiangping  Fang Ke  Liu Junchen  Cai Yongfeng  Deng Gui?an  Huang Xueqiang  Bai Ling?an  Qin Peng
Abstract:Fluid inclusions study and H-O-S isotopic geochemical analysis of ore and vein minerals were carried out in this study in order to reveal the characteristics of ore-forming fluid and material of the Chambishi copper deposit. The results of microscopic measurement of temperature show that the homogenization temperature and salinity of the fluid inclusions from hydrothermal fluid filling deposit mainly range from 100 to 350 ℃ and 11% to 19% NaCleqv, respectively. Analyses of H-O isotopic composition of the hydrothermal fluid filling deposit show that the values of δDV-SMOW and δ18OH2O are -64.0‰ to -52.6‰ and 1.57‰ to 2.97‰, respectively. Analyses of S isotopic composition show that the values of δ34SCDT from hydrothermal fluid filling orebodies and depositional orebodies are 5.5‰ to 12.1‰ and 6.0‰ to 21.0‰, respectively. The above data indicate that the ore-forming fluid of the hydrothermal fluid filling deposit is of medium-low temperature, low-middle salinity and density, and belongs to Cl-Na-Ca-type aqueous solution. The fluid is a mix of mantle and crust-derived magmas. Fluid mixing is the main reason for copper precipitation. Sulfur of the hydrothermal fluid filling deposit is similar to those of mantle-derived sulfur, whereas the sulfur of the depositional ore deposit is mainly sourced from diagenetic sulphide and seawater sulfate. The mechanism of sulfate reduction for both deposits is thermochemical reduction which resulted in the change of sulfur from SO42- to H2S. The mixed sources of ore-forming fluid and material indicate that mineralization of the hydrothermal fluid filling deposit is closely related to the middle Neoproterozoic magmatism, whereas mineralization of the depositional ore deposit is mainly related to the strong Late Neoproterozoic orogenesis and regional metamorphism. 
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