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Geology of gold ore deposits  105

            Table 2.3 Temperature±salinity conditions for selected hydrothermal ore deposits
            (after Huston, 1997)

            Temperature        Salinity               Ore type

            High (>300 ëC)     High (>10wt% NaCl)     Porphyry Cu-Au-Mo
            Low (<200ëC)       High (>10wt% NaCl)     MVT; Shale-hosted Pb-Zn-Ag
            Moderate (200±300ëC)  Moderate (5±10wt% NaCl)  VHMS Cu-Pb-Zn-Ag-Au
            High (>300 ëC)     Low (0±5 wt% NaCl)     Mesothermal Au
            Moderate (200±300ëC)  Low (0±5 wt% NaCl)  Epithermal Au-Ag



            Table 2.4 Relationships between temperature and redox conditions for selected
            hydrothermal type deposits (after Huston, 1997)

            Redox conditions  Gangue    Temperature           Ore type
            Highly oxidised  Hematite   Moderate (200±300 ëC)  Cu-U-hemitate
            (SO 4 -rich fluids)
            Oxidised        Magnetite/  High (>300 ëC)        Cu-Au-Fe oxide
            (SO 4 -rich fluids)  hematite
            Oxidised        Hematite/   Low (<200ëC)          Sediment-hosted
            (SO 4 -rich fluids)  pyrite
            Reduced         Pyrite      Moderate (200±300 ëC)  Au + pyrite; no Cu
            (H 2 S-rich fluids)
            Highly reduced  Pyrrhotite  High (>300 ëC)        Au-Cu-pyrrhotite
            (H 2 S-rich fluids)


            many times that value. The average values of selected country rocks from
            various sources are shown in Table 2.5.


            Fluid composition
            The relative concentrations of components such as sodium, potassium, calcium
            and magnesium reflect the equilibrium of fluid and rock within the hydrothermal
            system and can be used as geothermometers during geothermal exploration and
            exploitation (Giggenbach, 1992). Fluid compositions in steam heated waters in
            the surficial zone of active systems are strongly to moderately acid. Sulphate
            (derived from near surface oxidation of H 2 S) or bicarbonate dominate over
            chloride as the principal anion (Heinrich, 1989a).
              Phase separation resulting in the evolution of a gaseous systems phase is an
            important factor in gold ore formation due to significant changes to the
            chemistry of the residual brine, mainly through loss of volatiles such as H 2 S,
            CO 2 and H 2 and cooling of the residual brine. H 2 S loss causes Au deposition in
            dilute, low to moderate temperature, near-neutral fluids transporting Au as thio-
            complexes, for example in adularia-sericite epithermal systems.
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