22 research outputs found

    Mobilization of the platinum group elements by low-temperature fluids: Implications for mineralization and the iridium controversy

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    Geochemical investigations on the widely dispersed Late Proterozoic Acraman impact ejecta horizon and its host marine shales in the Adelaide Geosyncline provide strong evidence for low-temperature mobilization of the platinum group elements (PGE), including Ir. The ejecta horizon was formed when the middle Proterozoic dacitic volcanics in the Gawler Ranges, central South Australia, were impacted by a very large (ca. 4 km) meteorite. The resulting structure, now represented by Lake Acraman, is Australia's largest meteorite impact structure. Debris from the impact was blasted for many hundreds of kilometers, some falling into the shallow sea of the Adelaide Geosyncline, some 300 km to the east of the impact site

    Extreme enrichment of Se, Te, PGE and Au in Cu sulfide microdroplets: evidence from LA-ICP-MS analysis of sulfides in the Skaergaard Intrusion, east Greenland

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    The Platinova Reef, in the Skaergaard Intrusion, east Greenland, is an example of a magmatic Cu–PGE–Au sulfide deposit formed in the latter stages of magmatic differentiation. As is characteristic with such deposits, it contains a low volume of sulfide, displays peak metal offsets and is Cu rich but Ni poor. However, even for such deposits, the Platinova Reef contains extremely low volumes of sulfide and the highest Pd and Au tenor sulfides of any magmatic ore deposit. Here, we present the first LA-ICP-MS analyses of sulfide microdroplets from the Platinova Reef, which show that they have the highest Se concentrations (up to 1200 ppm) and lowest S/Se ratios (190–700) of any known magmatic sulfide deposit and have significant Te enrichment. In addition, where sulfide volume increases, there is a change from high Pd-tenor microdroplets trapped in situ to larger, low tenor sulfides. The transition between these two sulfide regimes is marked by sharp peaks in Au, and then Te concentration, followed by a wider peak in Se, which gradually decreases with height. Mineralogical evidence implies that there is no significant post-magmatic hydrothermal S loss and that the metal profiles are essentially a function of magmatic processes. We propose that to generate these extreme precious and semimetal contents, the sulfides must have formed from an anomalously metal-rich package of magma, possibly formed via the dissolution of a previously PGE-enriched sulfide. Other processes such as kinetic diffusion may have also occurred alongside this to produce the ultra-high tenors. The characteristic metal offset pattern observed is largely controlled by partitioning effects, producing offset peaks in the order Pt+Pd>Au>Te>Se>Cu that are entirely consistent with published D values. This study confirms that extreme enrichment in sulfide droplets can occur in closed-system layered intrusions in situ, but this will characteristically form ore deposits that are so low in sulfide that they do not conform to conventional deposit models for Cu–Ni–PGE sulfides which require very high R factors, and settling of sulfide liquids

    Major and minor elements composition of 5 manganese nodules and 2 sediment samples merged with compilation of previous manganese nodules analyses

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    Five manganese nodules from a range of deep-sea and fossil environments were selected for this study. Most samples were prepared for bulk analysis by grinding the material finely with a pestle in a porcelain mortar. However for samples Z2140 (ELT36.039-BT) and Timor (Wai_Bua_A) the nodule cores were discarded. Depending upon the chemical elements a varied range of analytical methods were used: X-Ray fluorescence, neutron activation, mass spectrometry and atomic absorption spectrometry. All samples were dried at 110°C for the determination of H2O+ loss. Structural water H2O- was determined by ignition at 1200°C (LOI) and total CO2 was measured by a Leco gasometric technique

    Analytical results on palagonite samples and manganese crusts from the Mid-Atlantic Ridge

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    A suite of three palagonites from pillowed basalts collected from within the Mid-Atlantic Ridge rift valley between 25°N and 30°N wer analysed along with another suite of two hydrothermally altered basaltic breccias and four hydrothermal manganese crusts collected from the TAG hydrothermal field at 26°N on the Mid-Atlantic Ridge. These specimen were collected during Trans-Atlantic Geotraverse (TAG) NOAA cruises using the R/V Discoverer. Two more hydrogenous ferromanganese crusts wer also analysed. They were collected from the eastern extension of the Atlantis Fracture Zone aboard the R/V Kurchatov in 1975. Radiochemical neutron activation analysis has been used to determine Tl, Rb. Cs. Co and Cr. Iron, Mn, and Mg concentrations in the crystalline samples and Mn crusts have been determined by AAS. K was determined by flame photometry, and S in these samples (as well as five glasses) has been determined with a Leco Automatic Sulfur titrator

    Analytical results on basalt samples from the Mid-Atlantic Ridge

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    A suite of eight glassy rims and six crystalline interiors from pillowed basalts was collected from within the Mid-Atlantic Ridge rift valley between 25°N and 30°N during Trans-Atlantic Geotraverse (TAG) NOAA cruises using the R/V Discoverer. Radiochemical neutron activation analysis has been used to determine Tl, Rb. Cs. Co and Cr. Major element and S analyses of the glasses were determined by electron probe microanalysts of small polished chips of glass

    Sulfur and selenium systematics of the subcontinental lithospheric mantle : inferences from the Massif Central xenolith suite (France)

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    Selenium has been analyzed in addition to S in 58 spinel peridotite xenoliths collected in Cenozoic alkali basalts from the Massif Central (France). The S concentration range now available for this suite, calculated from 123 samples, is the largest ever reported for alkali basalt-hosted xenoliths (<3–592 ppm). Likewise, the Se concentrations range between 0.2 and 67 ppb. No partial melting signature can be identified from the S and Se systematic. Half of the analyzed xenoliths have lost S during supergene weathering. By contrast, neither surficial alteration, nor loss of chalcophile elements during eruption can explain the regional-scale variations of S and Se concentrations. A first group of lherzolite xenoliths sampled in Southern Massif Central, from volcanic centers older and spatially unrelated to the Massif Central plume that triggered the Cenozoic volcanism, contains between 20 and 250 ppm S (with occasional S concentrations up to 592 ppm) and 12–67 ppb Se. It is clear that the highest S values, originally interpreted as representing S abundances in the primitive mantle, were in fact enriched by metasomatism. Highly variable S and Se contents (<5–360 ppm; 9–52 ppb) have also been observed in peridotite xenoliths collected in the Northern Massif Central, from volcanic centers mostly older than the plume. Like Group I xenoliths, these Group II xenoliths were strongly metasomatized by volatile-rich carbonated/silicated melts which precipitated Cu-rich sulfides. A third group of xenoliths from Plio-Quaternary basalts spatially related to the Massif Central Plume are uniformly poor in S (10–60 ppm) and Se (9–29 ppb). In this Group III, poikiloblastic textured xenoliths have lost most of their S and Se budget by peridotite-melt interactions at high melt/rock ratios. Taken as a whole, the Massif Central xenolith suite provides further evidence for strong heterogeneities in the S and Se budget of the sub-continental lithospheric mantle. However, the few LREE-depleted fertile lherzolites that escaped strong metasomatic alterations suggest a S- and Se-depleted primitive mantle reservoir compared to currently accepted primitive mantle estimates.15 page(s

    Rhenium-osmium systematics of the Mount Isa copper orebody and the Eastern Creek Volcanics, Queensland, Australia : implications for ore genesis

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    The syn-tectonic breccia-hosted Mount Isa Cu deposit in northwest Queensland is the largest sediment-hosted Cu deposit in Australia. Whole-rock samples of chalcopyrite-rich Cu ore form an isochron with a Re–Os age of 1,372 ± 41 Ma. This age is more than 100 Ma younger than the previously accepted age of Cu ore formation, an Ar–Ar mineral age for biotite separated from the host rocks within the alteration envelope to the Cu orebody. This discrepancy cannot be unequivocally resolved due to a lack of other absolute geochronological constraints for Cu mineralisation or the deformation event associated with Cu emplacement. The 1,372 ± 41 Ma date may reflect (a) the time of Cu deposition, (b) the time of a hydrothermal event that reset the Re–Os signature of the Cu ore or (c) mixing of the Re–Os isotope systematics between the host rocks and Cu-bearing fluids. However, a range of published Ar–Ar and Rb–Sr dates for potassic alteration associated with Cu mineralisation also records an event between 1,350 and 1,400 Ma and these are consistent with the 1,372 Ma Re–Os age. The 1.8 Ga Eastern Creek Volcanics are a series of tholeiitic basalts with a primary magmatic Cu enrichment which occur adjacent to the Mount Isa Cu deposit. The whole-rock Os isotopic signature of the Eastern Creek Volcanics ranges from mantle-like values for the upper Pickwick Member, to more radiogenic/crustal values for the lower Cromwell Member. The Re–Os isotope signature of the Cu ores overlaps with those calculated for the two volcanic members at 1,372 Ma; hence, the Os isotope data are supportive of the concept that the Os in the Cu ores was sourced from the Eastern Creek Volcanics. By inference, it is therefore postulated that the Eastern Creek Volcanics are the source of Cu in the Mount Isa deposit, as both Os and Cu are readily transported by oxidised hydrothermal fluids, such as those that are thought to have formed the Cu orebody. The Pickwick Member yields a Re–Os isochron age of 1,833 ± 51 Ma, which is within error of previously reported age constraints. The initial ¹⁸⁷Os/¹⁸⁸Os isotopic ratio of 0.114 ± 0.067 (γOs = −0.7) is slightly subchondritic, and together with other trace element geochemical constraints, is consistent with a subcontinental lithospheric mantle source. The Pickwick Member records a minimum age of ca. 1.95 Ga for melt depletion in the subcontinental lithospheric mantle beneath the Mount Isa Inlier prior to the extraction of the magmas which formed the Eastern Creek Volcanics. This corresponds with the end of subduction-related magmatism along the eastern margin of the Northern Australian Craton, which included the Mount Isa Inlier.21 page(s
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