Fluid chemistry and processes at the Porgera gold deposit, Papua New Guinea |
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| Authors: | J P Richards C J Bray D M DeR Channer E T C Spooner |
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| Institution: | (1) Department of Geology, University of Leicester, University Road, Leicester, LE1 7RH, UK, GB;(2) Department of Geology, University of Toronto, Earth Sciences Centre, 22 Russell St., Toronto, Ontario, M5S 3B1, Canada, CA |
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| Abstract: | The Porgera gold deposit in Papua New Guinea is a world-class example of an alkalic-type epithermal gold system (stage II),
which overprints a precursor stage of magmatic-hydrothermal gold mineralization (stage I). Gas and ion chromatographic analyses
of fluid inclusions contained in vein minerals from both mineralization stages have been carried out in order to constrain
the compositions of the fluids involved in, and the processes attending, ore deposition. These data indicate the presence
of three end-member liquids, the most dilute of which was present throughout the mineralization history and is interpreted
to represent evolved groundwater of meteoric origin. Its composition is estimated to have been approximately 500 mM Na+, 10 mM K+, 5 mM Li+, 250 mM Cl−, 0.15 mM Br−, and 0.01 mM I−, plus significant concentrations of dissolved gases. More saline liquids were also present during the two main stages of
ore formation, and although their compositions differ, both are interpreted to have been derived at least in part from magmatic
fluids, and to have been the media by which gold was introduced into the system. Stage I minerals contain fluid inclusions
which decrease in salinity towards this dilute end-member composition through the vein paragenesis, reflecting progressive
dilution at depth of the magmatic fluid source by groundwaters. Ore deposition is thought to have been caused largely by simple
cooling and/or wallrock reactions, although limited in situ fluid mixing may also have occurred. The most saline fluids, present
in early quartz and pyrite, contain at least 810 mM Na+, 530 mM Ca2+, 130 mM K+, 12 mM Li+, 87 mM SO4
2−, 960 mM Cl−, 1.1 mM Br−, and 0.05 mM I−, plus significant but variable concentrations of dissolved gases. Fluid inclusions from stage II hydraulic breccia veins
reveal the presence of two distinct liquids with contrasting salinities, which were present at different times during vein
formation. A higher salinity liquid appears to have predominated during mineralization, whereas lower salinity groundwaters
filled the structures during intervening periods. The ore-forming fluid may have been forcibly injected into the veins from
depth during fracturing and depressurization events, displacing the resident groundwaters in the process. The original composition
of this fluid is estimated to have been at least 1770 mM Na+, 59 mM K+, 180 mM Li+, 210 mM SO4
2−, 680 mM Cl−, 1.4 mM Br−, and 0.09 mM I−, plus 1.5 mol% CO2, 0.19 mol% CH4, and 0.04 mol% N2. Gas chromatographic analyses of fluid inclusions from stage II samples show a decrease in total gas content between early
unmineralized veins and post-mineralization vuggy quartz (suitable samples could not be obtained from the ore stage itself).
Post-mineralization samples plot along an experimental gas-saturation curve in the CO2-CH4-H2O-NaCl system, obtained at conditions similar to those attending stage II ore deposition at Porgera (200–300 bar, ˜165 °C).
These results are interpreted to indicate a period of depressurization-induced phase separation during hydraulic fracturing,
which resulted in rich ore deposition. Volatile gases such as CH4 and N2, in addition to CO2 in solution, are shown to have a significant negative effect on total gas solubility. This effect may be of critical importance
in lowering the temperature and increasing the depth (pressure) at which phase separation can occur in epithermal systems.
Received: 28 November 1995 / Accepted: 17 July 1996 |
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