1986
DOI: 10.2113/gsecongeo.81.8.2008
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Anomalous sulfur isotope compositions in the Golden Mile, Kalgoorlie

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Cited by 48 publications
(14 citation statements)
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“…Those with δ 34 S values more negative than -3 ‰ are variably accompanied by hypogene sulfate minerals (Sasaki et al, 1984;Goldfarb et al, 1991). Phillips et al (1986) found that the highly negative δ 34 S values for pyrites in gold-bearing quartz veins may occur under relatively oxidizing conditions of ore formation. However, no hypogene sulfate minerals have been identified in the veins or their igneous wall rocks in the Dongping deposit.…”
Section: Sulfur Isotopesmentioning
confidence: 99%
“…Those with δ 34 S values more negative than -3 ‰ are variably accompanied by hypogene sulfate minerals (Sasaki et al, 1984;Goldfarb et al, 1991). Phillips et al (1986) found that the highly negative δ 34 S values for pyrites in gold-bearing quartz veins may occur under relatively oxidizing conditions of ore formation. However, no hypogene sulfate minerals have been identified in the veins or their igneous wall rocks in the Dongping deposit.…”
Section: Sulfur Isotopesmentioning
confidence: 99%
“…Golden Mile mineralization is hosted by a differentiated basic igneous intrusion (the Golden Mile Dolerite), and has two well-documented features which are found in only a small number of Archean gold deposits. One is the presence of pyrite with moderately negative δ 34 S isotope values (-10 to -2‰; Lambert et al, 1984;Phillips et al, 1986;Cameron and Hattori, 1987;Bateman and Hagemann, 2004). Such negative values differ from the 0 ± 4 per mil values for pyrite in the Paringa basalt adjacent to the Golden Mile Dolerite, the Mount Charlotte deposit, which is also in the Golden Mile Dolerite within the Kalgoorlie gold field, and most other Archean greenstone gold deposits (Lambert et al, 1984).…”
Section: Introductionmentioning
confidence: 99%
“…The negative sulfur isotopes have been interpreted as a record of the presence of aqueous sulfate during ore deposition (Golding and Wilson, 1983;Phillips et al, 1986). The sulfate is thought to have been a product of oxidization that also produced hematite from preexisting magnetite; however, the cause of the oxidation and the role that it played in ore deposition is not well known (compare Phillips et al, 1986, andCameron, 1988).…”
Section: Introductionmentioning
confidence: 99%
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“…7), because sulphides in oxidised systems can display substantial negative fractionation from the ~34S value of the fluid. However, such systems commonly also show a wide isotopic range (Large 1975, Scott et al 1985, Phillips et al 1986. In this instance the narrow negative range may therefore favour a thermally-degraded organic sulphur source, or dissolution of "open system" biogenic pyrite.…”
Section: "mentioning
confidence: 99%