Spatial Association Between Platinum Minerals and Magmatic Sulfides Imaged with the Maia Mapper and Implications for the Origin of the Chromite-Sulfide-PGE Association

ABSTRACT The spatial association between Pt minerals, magmatic sulfides, and chromite has been investigated using microbeam X-ray fluorescence (XRF) element mapping and the Maia Mapper. This lab-based instrument combines the Maia parallel energy dispersive (ESD) detector array technology with a focused X-ray beam generated from a liquid metal source. It proves to be a powerful technique for imaging Pt distribution at low-ppm levels on minimally prepared cut rock surfaces over areas of tens to hundreds of square centimeters, an ideal scale for investigating these relationships. Images of a selection of samples from the Bushveld Complex and from the Norilsk-Talnakh ore deposits (Siberia) show strikingly close association of Pt hotspots, equated with the presence of Pt-rich mineral grains, with magmatic sulfide blebs in all cases, except for a taxitic low-S ore sample from Norilsk. In all of the Bushveld samples, at least 75% of Pt hotspots (by number) occur at or within a few hundred microns of the outer edges of sulfide blebs. In samples from the leader seams of the UG2 chromitite, sulfides and platinum hotspots are also very closely associated with the chromite seams and are almost completely absent from the intervening pyroxenite. In the Merensky Reef, the area ratio of Pt hotspots to sulfides is markedly higher in the chromite stringers than in the silicate-dominated lithologies over a few centimeters either side. We take these observations as confirmation that sulfide liquid is indeed the prime collector for Pt and, by inference, for the other platinum group elements (PGEs) in all these settings. We further propose a mechanism for the sulfide-PGE-chromite association in terms of in situ heterogeneous nucleation of all these phases coupled with transient sulfide saturation during chromite growth and subsequent sulfide loss by partial re-dissolution. In the case of the amygdular Norilsk taxite, the textural relationship and high PGE/S ratio is explained by extensive loss of S to an escaping aqueous vapor phase.

Petrological and geochemical characterization of the arc-related Suru–Thasgam ophiolitic slice along the Indus Suture Zone, Ladakh Himalaya

The Ladakh Himalayan ophiolites preserve remnants of the eastern part of the Neo-Tethyan Ocean, in the form of Dras, Suru Valley, Shergol, Spongtang and Nidar ophiolitic sequences. In Kohistan region of Pakistan, Muslim Bagh, Zhob and Bela ophiolites are considered to be equivalents of Ladakh ophiolites. In western Ladakh, the Suru–Thasgam ophiolitic slice is highly dismembered and consists of peridotites, pyroxenites and gabbros, emplaced as imbricate blocks thrust over the Mesozoic Dras arc complex along the Indus Suture Zone. The Thasgam peridotites are partially serpentinized with relict olivine, orthopyroxene and minor clinopyroxene, as well as serpentine and iron oxide as secondary mineral assemblage. The pyroxenites are dominated by clinopyroxene followed by orthopyroxene with subordinate olivine and spinel. Gabbros are composed of plagioclase and pyroxene (mostly replaced by amphiboles), describing an ophitic to sub-ophitic textural relationship. Geochemically, the studied rock types show sub-alkaline tholeiitic characteristics. The peridotites display nearly flat chondrite-normalized rare earth element (REE) patterns ((La/Yb)N = 0.6–1.5), while fractionated patterns were observed for pyroxenites and gabbros. Multi-element spidergrams for peridotites, pyroxenites and gabbros display subduction-related geochemical characteristics such as enriched large-ion lithophile element (LILE) and depleted high-field-strength element (HFSE) concentrations. In peridotites and pyroxenites, highly magnesian olivine (Fo88.5-89.3 and Fo87.8-89.9, respectively) and clinopyroxene (Mg no. of 93–98 and 90–97, respectively) indicate supra-subduction zone (SSZ) tectonic affinity. Our study suggests that the peridotites epitomize the refractory nature of their protoliths and were later evolved in a subduction environment. Pyroxenites and gabbros appear to be related to the base of the modern intra-oceanic island-arc tholeiitic sequence.

Deciphering the brittle failure of eclogites at high-pressures: hydrofractures as fluid-escape pathways

<p>The Tsäkkok lens (northern Scandinavian Caledonides) represents the outermost part of the rifted Baltica passive margin and consists of sediments and pillow basalts of MORB affinity that were metamorphosed in eclogite facies. The Tsäkkok eclogites underwent metamorphism in a cold subduction regime (~8 °C/km) at the onset of the Iapetus Ocean closure. These rocks record pervasive high-pressure, fracturing during prograde dehydration at eclogite-facies conditions reaching up to 2.2 GPa and 590 ºC. Locally, the omphacite-dominated groundmass is transected by fractures sealed either by omphacitite or garnetite veins. Garnetite veins form a dense network that disrupt intact eclogite blocks, whereas omphacitite is found in rare, single veins. The garnetite veins are dominated by dense, poikiloblastic garnet clusters and display two chemically different zones, i.e., a high-Mn inner zone and a low-Mn outer zone. Detailed microstructural and geochemical mapping by EDS-EBSD SEM revealed that the high-Mn inner zone is disrupted and sealed by the low-Mn garnet zone. Garnets in the vein usually show little elongation and moderate intracrystalline substructure that is dominated by slightly changing misorientations without clear subgrain boundaries. By contrast, garnets of the sealed domain display an abrupt grain size reduction and anomalously high density of sharp intracrystalline misorientations in equant grains. The interstitial space between garnet grains in both of the inner and outer zones of the vein is infilled by omphacite + rutile + quartz + phengite + glaucophane.</p><p>The textural relationship between the inner- and outer zones of the garnetite vein implies syn-deformation growth of the outer zone, while the mineral assemblage attests for high-pressure conditions of the vein formation. Considering the lack of significant offset along the vein, we interpret the observed microstructures as formed during the sudden opening and closing of a brittle fracture, typical of hydrofracturing, and fast crystal growth assisted by high-pressure fluids. Presumably, these fractures constitute a fluid escape pathway during dehydration at prograde/peak conditions.</p><p>Research funded by NCN project no. 2019/33/N/ST10/01479 (M.Bukała) and no. 2014/14/E/ST10/00321 (J.Majka), as well as the The Polish National Agency for the Academic Exchange scholarship no. PPN/IWA/2018/1/00046/U/0001 given to M.Bukała.</p><p> </p>

MINERAL CHEMISTRY AND GEOCHEMISTRY OF HYPERSTHENE-BEARING DIORITE FROM ERUSU AKOKO, SOUTHWESTERN NIGERIA

Samples of mafic intrusive rock were analyzed for their mineralogical and chemical properties. The textural relationship was studied using the petrographic microscope, elemental composition of minerals was determined using the Electron Microprobe and the whole rock chemical analysis was done using the XRF and ICP-MS. The following minerals were observed in order of abundance; pyroxene, amphibole, plagioclase, biotite, opaque minerals, quartz and chlorite, with apatite and zircon occurring as accessory mineral. Two types of pyroxenes were observed; orthopyroxene (hypersthene) and clinopyroxene. Texturally, amphiboles have inclusions of plagioclase and pyroxene. The plagioclase has undergone sericitization. The chemical composition of the pyroxene is En51.95Fs44.53Wo3.52, biotite has Fe/(Fe+Mg):0.42, Mg/(Fe+Mg):0.59, and plagioclase is Ab63.5An34.55Or1.95. Whole rock chemistry shows a chemical composition; SiO2: 45.15 %, Al2O3: 14.04 %, Fe2O3: 16.01 %, MgO: 5.65 %, CaO: 7.58 % and TiO2: 3.59 %. There is an enrichment of LREE and a depletion of HREE. Based on the minerals, mineral chemistry and the geochemistry of the studied rock, the rock is mafic and hydrous minerals formed by hydration recrystallization of pyroxene. The rock has extensively retrogressed but has not been affected by any form of deformation.

Prograde polyphase regional metamorphism of pelitic rocks, NW of Jamshedpur, eastern India: constraints from textural relationship, pseudosection modelling and geothermobarometry

The study area belongs to the Singhbhum metamorphic belt of Jharkhand, situated in the eastern part of India. The spatial distribution of the index minerals in the pelitic schists of the area shows Barrovian type of metamorphism. Three isograds, viz. garnet, staurolite and sillimanite, have been delineated and the textural study of the schists has revealed a time relation between crystallization and deformation. Series of folds with shifting values of plunges in the supracrustal rocks having axial-planar schistosity to the folds have been widely cited. Development of these folds could be attributed to the second phase of deformation. In total, two phases of deformation, D1 and D2, in association with two phases of metamorphism, M1 and M2, have been lined up in the study area. Chemographic plots of reactant and product assemblages corresponding to various metamorphic reactions suggest that the pattern of metamorphic zones mapped in space is in coherence with the temporal-sequential change during prograde metamorphism. The prograde P–T evolution of the study area has been obtained using conventional geothermobarometry, internally consistent winTWQ program and Perple_X software in the MnNCKFMASHTO model system. Our observations suggest that the progressive metamorphism in the area is not related to granitic intrusion or migmatization but that it was possibly the ascending plume that resulted in the M1 phase of metamorphism followed by D1 deformation. The second and prime metamorphic phase, M2, with its possible heat source generated by crustal overloading, was preceded by D1 and it lasted until late- to post-D2 deformation.

Optical image and microchemical analysis of gold grains from a weathered profile of the Minvoul greenstone belt, northern Gabon

Morphological characterization and quantification of gold particles by optical image analysis (OIA) and by compositional analysis of microprobes using scanning electron microscope and electron microprobe analysis techniques were carried out on gold grains from the Minvoul area (Archean greenstone belt in Gabon). Large grains of almost pure gold were found throughout a weathering profile, which consisted of saprolite, mottled clay zone, iron duricrust, pisolitic gravels and yellow latosol. In the deeper horizons, gold was dissolved as shown by corrosion features on the surface of particles with average sizes of 2.6Φ and 2.35Φ in the saprolite and mottled clay zones, respectively. The occurrence of secondary gold in the duricrust was indicated by the larger size of the nuggets (average, 1.8Φ), the high fineness (> 995 in average) and the close textural relationship between gold and neoformed iron oxyhydroxides. The uppermost horizons composed of yellow latosol and pisolitic gravels were interpreted as transported materials based on their size distribution (average 0.85Φ and 1.34Φ), sorting and shape parameters. The best morphological parameter to describe the whole weathering profile was found to be the perimeter/area ratio. The highest ratios were recorded in the saprolite (average 0.192 μm−1), and decreased towards the surface (average 0.057 μm−1). The combination of the OIA technique and the microchemical analysis of gold grains allowed us to define specific morphological and compositional characteristics of the gold particles for each horizon. Both methods proved to be of great utility to understand gold concentration, dissolution and dispersion processes in supergene environments.