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Platinum-group element geochemistry of the Forest Reef Volcanics, southeastern Australia: Implications for porphyry Au-Cu mineralisation

dc.contributor.authorLowczak, Jessica N.
dc.contributor.authorCampbell, Ian H.
dc.contributor.authorCocker, Helen
dc.contributor.authorPark, Jung-Woo
dc.contributor.authorCooke, David R.
dc.date.accessioned2018-01-08T05:01:11Z
dc.date.issued2018
dc.description.abstractPlatinum-group element concentrations in felsic to intermediate rocks from the Forest Reef Volcanics, Cadia-Neville region, southeastern Australia have been analysed by the Ni-S fire assay-isotope dilution method. The Forest Reef Volcanics are shoshonitic to calc-alkaline in composition and fractionated to produce a wide range of compositions, with MgO varying between 9.7 and 1.8 wt.%. The interest in this suite is that it is coeval with Au-Cu porphyry-style mineralisation in the Cadia mineral district. This study uses PGE geochemistry to determine the timing of sulfide saturation, relative to volatile (ore-fluid) saturation, in the magma that gave rise to the Forest Reef Volcanics and, in turn, to assess how this timing affected the mineralisation potential of the evolving magmatic system. The Forest Reef Volcanics can be subdivided, on the basis of their contrasting PGE geochemistry, into high-Mg (>6.8 wt.% MgO) and low-Mg suites (≤6.8 wt.% MgO). Platinum, Pd and Re concentrations increase in the high-Mg samples, whereas Ir and Ru decrease and Rh concentrations remain steady, with decreasing MgO. The coupled Ir, Ru and Rh depletion is attributed to the partitioning of these elements into magnetite. The rate of Pt and Pd enrichment is not possible by closed-system fractional crystallisation alone, which suggests that the parent magma was replenished by a Pt-Pd-rich melt. In contrast, the PGE concentrations in the low-Mg samples decrease with decreasing MgO indicating the onset of sulfide saturation at 6.8 wt.% MgO, which is confirmed by the presence of spheroidal sulfide inclusions in liquidus crystals (i.e. clinopyroxene, plagioclase, magnetite). The rate of Pd depletion is appreciably less than for any other sulfide saturated felsic system for which data are available. This requires either that the amount of sulfide melt to have precipitated was unusually low, or that the rate of Pd depletion was limited by the mass of silicate melt the sulfide melt reached equilibrium with, or both. In any event, the fraction of sulfide melt that precipitated was too small to have had a significant effect on the Cu and Au content of the magma so that both Cu and Au were available to enter the ore-forming fluid when the magma became volatile saturated at, or shortly after, it reached ca. 2.9 wt.% MgO.en_AU
dc.description.sponsorshipThis research was funded by a Newcrest Mining LTD Grant to Ian Campbell.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0016-7037en_AU
dc.identifier.urihttp://hdl.handle.net/1885/139092
dc.publisherElsevieren_AU
dc.rights© 2017 Elsevier B.V. http://www.sherpa.ac.uk/romeo/issn/0016-7037/..."Author's post-print on open access repository after an embargo period of between 12 months and 48 months" from SHERPA/RoMEO site (as at 8/01/18).en_AU
dc.sourceGeochimica et Cosmochimica Actaen_AU
dc.titlePlatinum-group element geochemistry of the Forest Reef Volcanics, southeastern Australia: Implications for porphyry Au-Cu mineralisationen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.lastpage406en_AU
local.bibliographicCitation.startpage385en_AU
local.contributor.affiliationLowczak, J. N., Research School of Earth Sciences, The Australian National Universityen_AU
local.contributor.affiliationCampbell, I. H., Research School of Earth Sciences, The Australian National Universityen_AU
local.contributor.affiliationCocker, H., Research School of Earth Sciences, The Australian National Universityen_AU
local.contributor.affiliationPark, J.-W., Research School of Earth Sciences, The Australian National Universityen_AU
local.identifier.ariespublicationu4351680xPUB339
local.identifier.citationvolume220en_AU
local.identifier.doi10.1016/j.gca.2017.09.052en_AU
local.publisher.urlhttps://www.elsevier.com/en_AU
local.type.statusAccepted Versionen_AU

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