Fluid inclusions and C-H-O-S isotope systematics of early Permian porphyry Mo mineralization of the West Junggar region,NW China: the Suyunhe example

ABSTRACT

The Suyunhe porphyry Mo deposit, located in the West Junggar terrane, is the largest molybdenum deposit found in Xinjiang to date, with a proven reserve of 0.57 Mt. The Suyunhe deposit is associated with Early Permian granitic rocks, which emplaced into the volcano-sedimentary sequences of the Middle Devonian Barluk Formation. Four metallogenic stages are identified in this study. Stage I is marked by the quartz-magnetite-K-feldspar±biotite±pyrite±molybdenite veins, which mainly occurred in the intensively potassic alternation zone and were formed at high temperature (>481°C), high salinity (58.6?65.18 wt.%), and relatively high oxygen fugacity conditions with a fluid system of NaCl-H₂O-CO₂. Stage II is the main metallogenic stage and develops numerous quartz-molybdenite±pyrite veins associated with muscovite–chlorite alteration, which were formed by immiscible fluids at medium-high temperature (210?427°C), medium-high salinity (43.36?49.90 wt.%), and relatively low oxygen fugacity conditions with the fluid system of NaCl-H₂O-CO₂-CH₄-C₂H₆. After the main Mo-mineralization, quartz-polymetallic sulphides veins associated with quartz–sericite alteration were formed by fluids at medium-low temperature, low-salinity conditions with the fluid system of NaCl-H₂O-CO₂ in stage III. The following quartz-polymetallic sulphide veins are quartz-calcite±pyrite veins associated with calcite alteration, which were formed by fluids at low temperature and low-salinity conditions with a fluid system of NaCl-H₂O in stage IV.

The δ¹⁸O‰ values indicate that the ore fluids of stages I and II are dominated by magmatic water, whereas stages III and IV are dominated by meteoric water. A wide range of δ³⁴S‰ values (?7.1 to 3.4‰) of sulphides between stages I and II indicates that increasing the reducibility plays an important role in molybdenum mineralization. The δ¹³C_CH4 values suggest that CH₄ of the ore fluids mainly results from the assimilation–contamination of carbonaceous country rocks, and partly derives from magma. However, the δ¹³C_CO2 values suggest that CO₂ of the ore fluids mainly originates from magma, and minor derives from wall-rocks as well as meteoric water.