Co-precipitation of gold and base metal sulfides during fluid boiling triggered by fault-valve processes in orogenic gold deposits

Abstract

The extreme fluctuations in pressure during earthquakes are widely regarded as responsible for gold mineralization in quartz-vein-hosted gold deposits. However, it is barely noticed that base metal sulfides can precipitate together with gold during these processes. Here we present the phenomenon and unravel the mechanism of the co-precipitation of Au and base metal sulfides during the fluid boiling via geological study and thermodynamic modeling, respectively. The Bangbu deposit, a lode-type orogenic gold deposit in Tibet shows two mineralization substages of pyrite. The pyrite formed in the later substage is hosted in the wall rock selvages of laminated crack-seal quartz veins formed by the fault-valve processes. The pyrite grains are characterized by anhedral small crystals with porous textures and abundant native gold, chalcopyrite, galena, and sphalerite inclusions. They also contain higher concentrations of Cu, Pb, Ag, Sb, and Au, and lower concentrations of Co and Ni, compared to the euhedral large-grained pyrite formed in the initial substage. The textural and trace element characteristics of the pyrite indicate that vigorous boiling occurred during fault-valve behavior, which decreased the solubilities of Au, Cu, Pb, and Zn in the ore fluid in Bangbu. The co-precipitation of Au and base metal sulfides triggered by fluid boiling has also been reported in other orogenic gold deposits worldwide.Thermodynamic models are designed to acquire the predominant species and solubility of Au, Cu, Pb, and Zn in orogenic ore fluids under varied chemical conditions. The results show that Au, Cu, Pb, and Zn are dominantly transported as hydrosulfide complexes under lower mesozonal to epizonal deposit conditions. At temperatures of about above 350 °C, Au hydrosulfide species still predominates, but the predominant Cu, Pb, and Zn species change from hydrosulfide to chloride complexes. A sudden decrease in the reduced sulfur concentration during fluid boiling may be the most important mechanism controlling the precipitation of Au, Cu, Pb, and Zn in lower mesozonal to epizonal deposits. The decrease of logfS2 during fluid boiling can increase the fluid pH, resulting in the decrease of solubilities of base metal chloride complexes and thus explain the co-precipitation of Au and base metal sulfides in hypozonal deposits.