Genesis of Kanggur Gold Deposit in Eastern Tianshan Orogenic Belt, NW China: Fluid Inclusion and Oxygen and Hydrogen Isotope Constraints
Zhiliang Wang, Neng Jiang, Yitian Wang, Jingwen Mao, Jianmin Yang
Abstract
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Zhiliang Wang, Neng Jiang, Yitian Wang, Jingwen Mao, Jianmin Yang
Abstract
Open-access reader
Abstract. Primary fluid inclusions in quartz and carbonates from the Kanggur gold deposit are dominated by aqueous inclusions, with subsidiary CO2‐H2O inclusions that have a constant range in CO2 content (10–20 vol %). Microthermometric results indicate that total homogenization temperatures have a wide but similar range for both aqueous inclusions (120d̀ to 310d̀C) and CO2‐H2O inclusions (140d̀ to 340d̀C). Estimates of fluid salinity for CO2‐H2O inclusions are quite restricted (5.9∼10.3 equiv. wt% NaCl), whereas aqueous inclusions show much wider salinity ranging from 2.2 to 15.6 equivalent wt %NaCl. The 6D values of fluid inclusions in carbonates vary from ‐45 to ‐61 %, in well accord with the published δD values of fluid inclusions in quartz (‐46 to ‐66 %). Most of the δ18O and δD values of the ore‐forming fluids can be achieved by exchanged meteoric water after isotopic equilibration with wall rock by fluid/rock interaction at a low water/rock ratio. However, the exchanged meteoric water alone cannot explain the full range of δ18O and δD values, magmatic and/or meta‐morphic water should also be involved. The wide salinity in aqueous inclusions may also result from mixing of meteoric water and magmatic and/or metamorphic water.
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Abstract. Primary fluid inclusions in quartz and carbonates from the Kanggur gold deposit are dominated by aqueous inclusions, with subsidiary CO2‐H2O inclusions that have a constant range in CO2 content (10–20 vol %). Microthermometric results indicate that total homogenization temperatures have a wide but similar range for both aqueous inclusions (120d̀ to 310d̀C) and CO2‐H2O inclusions (140d̀ to 340d̀C). Estimates of fluid salinity for CO2‐H2O inclusions are quite restricted (5.9∼10.3 equiv. wt% NaCl), whereas aqueous inclusions show much wider salinity ranging from 2.2 to 15.6 equivalent wt %NaCl. The 6D values of fluid inclusions in carbonates vary from ‐45 to ‐61 %, in well accord with the published δD values of fluid inclusions in quartz (‐46 to ‐66 %). Most of the δ18O and δD values of the ore‐forming fluids can be achieved by exchanged meteoric water after isotopic equilibration with wall rock by fluid/rock interaction at a low water/rock ratio. However, the exchanged meteoric water alone cannot explain the full range of δ18O and δD values, magmatic and/or meta‐morphic water should also be involved. The wide salinity in aqueous inclusions may also result from mixing of meteoric water and magmatic and/or metamorphic water.
Key concepts: Fluid inclusions, Meteoric water, Geology, Quartz, Salinity, Geochemistry, Magmatic water, Inclusion (mineral)