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Molybdenum isotopic composition as a tracer for low-medium temperature hydrothermal ore-forming systems: A case study on the Dajiangping pyrite deposit, western Guangdong Province, China TEXT SIZE: A A A

Little is known about the range or controls on the molybdenum isotopic composition of low-medium temperature hydrothermal ore-forming systems. We present molybdenum isotope data from 12 hydrothermal syndepositional silicalite and carbonaceous slate samples from the Dajiangping pyrite deposit in western Guangdong Province, South China. The delta (97/95) Mo values from Orebody III range from -0.02aEuro degrees to 0.29aEuro degrees, with an average of 0.18aEuro degrees. In contrast, the composition values from Orebody IV display a larger variation from -0.70aEuro degrees to 0.62aEuro degrees. However, the five samples from the main ore bed all show strong negative values. This indicates that the significant variation in molybdenum isotopic composition supports different hydrothermal ore-forming metallogenesis and a metallogenic environment between the two orebodies. Orebody III is likely to have been deposited from submarine exhalative hydrothermal fluids under a relatively strong reducing environment and Orebody IV may have also been influenced by hydrothermal superimposition in a more oxidized disequilibrium condition. In addition, the delta (97/95) Mo values of Orebody IV are clearly negative, together with the values increasing stratigraphically upward in the ore beds, suggesting that the metallogenic environment of Orebody IV is different from the open oceanic systems. There might be dynamic fractionation in this restricted environment. Therefore, the molybdenum isotope can be used as an effective tracer for the ore-forming fluid and metallogenic environment.

 Publication name  CHINESE SCIENCE BULLETIN Volume:56  Issue:21  Pages:2221-2228  Published:JUL 2011
 Author(s)  Song ShiMing; Hu Kai; Wen HanJie; Zhang YuXu; Li Kuang; Fan HaiFeng
 Corresponding author  

 HU Kai
 kaihu@nju.edu.cn
 Nanjing Univ, Sch Earth & Engn, State Key Lab Mineral Deposits Res, Nanjing 210093, Peoples R China

 Author(s) from IGCAS  WEN Hanjie,  ZHANG Yuxu,  FAN Haifeng

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