PRECIOUS VAPOR: METAL TRANSPORT IN MAGMATIC-HYDROTHERMAL SYSTEMS
New formulations of metal solubility in low- and intermediate-density fluids based on experimental data [2-5], allow for the thermodynamic modeling of metal solubility and mineral precipitation during cooling and decompression of a magmatic high temperature volatile phase [6]. Geochemical simulations were performed using GEM-Selektor [7] and metal mobility was modeled in the context of Cu-Au-Mo porphyry and Au-Ag epithermal ore formation. Metal solubility as a function of T, P, redox condition, sulfur and HCl contents was evaluated, showing the interplay of these variables in dictating metal budgets and zoning in ore deposits. During cooling and decompression of an intermediate-density fluid, Au concentration reaches a maximum at 460 °C and Cu at 540 °C, whereas Mo and Ag concentrations decrease with decreasing T and P. The solubility maximum of gold occurs at 340 °C at lower fluid density indicating a potential for remobilization/redistribution of gold to shallower, and more distal environments. The redox condition at high temperatures is buffered by the vein mineral assemblage of magnetite-rutile-anhydrite or magnetite-rutile-anhydrite-pyrite. The presence of pyrite indicates that sulfur contents of the magmatic fluids are as high as 4-6 wt.%, whereas anhydrite stability occurs at sulfur contents of 0.2 wt.%. The sulfur content and redox condition control the metal ratios of the magmatic fluids and therefore the overall metal budget of the ore deposit.
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