Mineralogy, geochemistry and emplacement of the Conakry Igneous Complex, Guinea: implications for the Ni–Cu–PGE mineralization

2018 ◽  
Vol 82 (3) ◽  
pp. 593-624
Author(s):  
Thierry Augé ◽  
Éric Gloaguen ◽  
Matthieu Chevillard ◽  
Laurent Bailly
Keyword(s):  
Dynamic Environment ◽  
Massive Sulfide ◽  
Sulfide Liquid ◽  
Form Complex ◽  
Igneous Complex ◽  
Almost Everywhere ◽  
Platinum Group Minerals ◽  
Pge Mineralization ◽  
Ultramafic Intrusion ◽  
Magmatic Sulfide

ABSTRACTThe Conakry Igneous Complex is a mafic-ultramafic intrusion emplaced contemporaneously with the opening of the Atlantic, forming a complex, 55 km x 5 km dyke-like body within which three main episodes of injection have been recognized, characterized by a lack of mineral layering. Unit 1 consists of dunite and related facies, Unit 2 of wehrlite and pyroxene peridotite and Unit 3 corresponds to various gabbro facies. Units 1 and 2 constitute the Kaloum Peninsula; Unit 3 is its NW extension, forming the 1010 m high Mount Kakoulima. Unit 3 intrudes the two previous units and corresponds to a tholeiitic liquid that crystallized in an almost closed system, and thus exhibits a strong differentiation trend, in contrast to Units 1 and 2. Mineral compositions suggest the existence of a deeper magma chamber where a first stage of differentiation occurred.Disseminated base-metal sulfides (BMS) are present in all units of the complex and earlier descriptions have mentioned a “massive sulfide layer” with 2 to 4 g/t PGE. Platinum-group minerals (PGM) are almost everywhere included in or attached to composite Ni–Fe–Cu sulfides. Most PGM grains form complex associations resulting either from exsolution or alteration. It is characteristic of the Conakry Igneous Complex PGM, described here for the first time, to be dominated by (Pd,Pt)(Te,Bi) minerals with rare Pd,Sn and Pd,Pb compositions and an absence of Pt,Pd sulfides and Pt,Pd antimonides.The constant association of the PGM with the BMS shows that the magmatic sulfide liquid acts as an efficient collector of PGE. In such a dynamic environment, the process leading to the formation of massive sulfides must be sought in the accumulation of sulfides in the conduit following host-rock assimilation. Accordingly, considering the multiple injection processes that characterize the whole intrusion, the potential for discovering additional Ni–Cu–PGE mineralization in the Conakry Igneous Complex remains high.

Ni-Cu sulfide mineralization and PGM from the Samapleu mafic-ultramafic intrusion, Yacouba complex, western Ivory Coast

2021 ◽  
Vol 59 (4) ◽  
pp. 631-665
Author(s):  
Franck Gouedji ◽  
Christian Picard ◽  
Marc Antoine Audet ◽  
Thierry Augé ◽  
Jorge Spangenberg
Keyword(s):  
Ivory Coast ◽  
Massive Sulfide ◽  
Sulfide Mineralization ◽  
Platinum Group Minerals ◽  
Thermo Fisher Scientific ◽  
Mass Spectrometer System ◽  
Ultramafic Intrusion ◽  
Platinum Group ◽  
Mineralizing Process ◽  
Spectrometer System

ABSTRACT The mafic-ultramafic Samapleu deposits of the Yacouba complex, which host nickel, copper sulfides, and platinum-group minerals, are located in the Biankouma-Silipou region, western Ivory Coast. These intrusions originate from the mantle and would have been established during the Proterozoic (2.09 Ga) around 22 km deep within the Archean granulites (3.6–2.7 Ga) which at least partially contaminated them. Platinum-group and sulfide minerals from the Samapleu deposits were studied using optical microscopy, scanning electron microscopy, the electronic microprobe, X-ray fluorescence, fire assay, and a Thermo Fisher Scientific Delta S isotope ratio mass spectrometer system. The sulfide mineralization (mainly pyrrhotite, pentlandite, chalcopyrite ± pyrite) is mainly disseminated with, in places, semi-massive to massive sulfide veins. It is especially abundant in pyroxenite horizons with net or breccia textures. The isotopic ratios of sulfur measured from the sulfides (an average of 0.1‰), the R factor (between 1500 and 10,000), and the Cu/Pd ratios indicate a mantle source. Thus, the sulfides would have formed from sulfide liquids produced by immiscibility from the silicate mantle magma under mafic-ultramafic intrusion emplacement conditions and with possible geochemical modification of the magmas by assimilation of the surrounding continental crust. The platinum-group minerals (michenerite, merenskyite, moncheite, Co-rich gersdorffite, irarsite, and hollingworthite) are mainly associated with the sulfide phases. The nature of the platinum-group minerals is indicative of the probable role of late-magmatic hydrothermal fluids during the mineralizing process.

scholarly journals Composition of iron oxides in Archean and Paleoproterozoic mafic-ultramafic hosted Ni-Cu-PGE deposits in northern Fennoscandia: application to mineral exploration

2020 ◽  
Vol 55 (8) ◽  
pp. 1515-1534
Author(s):  
M. Moilanen ◽  
E. Hanski ◽  
J. Konnunaho ◽  
T. Törmänen ◽  
S.-H. Yang ◽  
...  
Keyword(s):  
Trace Element ◽  
Iron Oxides ◽  
Oxide Phase ◽  
Massive Sulfide ◽  
Sulfide Liquid ◽  
Monosulfide Solid Solution ◽  
Sulfide Deposits ◽  
Northern Fennoscandia ◽  
Pge Mineralization ◽  
Wide Range

Abstract Using electron probe microanalyzer (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), we analyzed major and trace element compositions of iron oxides from Ni-Cu-PGE sulfide deposits hosted by mafic-ultramafic rocks in northern Fennoscandia, mostly focusing on Finland. The main research targets were the Archean Ruossakero Ni-(Cu) deposit; Tulppio dunite and related Ni-PGE mineralization; Hietaharju, Vaara, and Tainiovaara Ni-(Cu-PGE) deposits; and Paleoproterozoic Lomalampi PGE-(Ni-Cu) deposit. In addition, some reference samples from the Pechenga (Russia), Jinchuan (China), and Kevitsa (Finland) Ni-Cu-PGE sulfide deposits, and a barren komatiite sequence in the Kovero area (Finland) were studied. Magnetite and Cr-magnetite show a wide range of trace element compositions as a result of the variation of silicate and sulfide melt compositions and their post-magmatic modification history. Most importantly, the Ni content in oxide shows a positive correlation with the Ni tenor of the sulfide phase in equilibrium with magnetite, regardless of whether the sulfide assemblage is magmatic or post-magmatic in origin. The massive sulfide samples contain an oxide phase varying in composition from Cr-magnetite to magnetite, indicating that Cr-magnetite can crystallize directly from sulfide liquid. The Mg concentration of magnetites in massive sulfide samples is lowest among the samples analyzed, and this can be regarded as a diagnostic feature of an oxide phase crystallized together with primitive Fe-rich MSS (monosulfide solid solution). Our results show that magnetite geochemistry, plotted in appropriate discrimination diagrams, together with petrographical observations could be used as an indicator of potential Ni-(Cu-PGE) mineralization.

Compositions and Ni-Cu-Platinum Group Element Tenors of Nova-Bollinger Ores with Implications for the Origin of Pt Anomalies in Platinum Group Element-Poor Massive Sulfides

2022 ◽  
Author(s):  
Stephen J. Barnes ◽  
Clifford R. Stanley ◽  
Valentina Taranovic
Keyword(s):  
Platinum Group Element ◽  
Massive Sulfide ◽  
Group Element ◽  
Sulfide Liquid ◽  
Partial Explanation ◽  
Sampling Artifacts ◽  
Platinum Group Minerals ◽  
Liquid Fractionation ◽  
Platinum Group ◽  
Relative Errors

Abstract The Nova-Bollinger Ni-Cu-platinum group element (PGE) deposit in the Fraser zone of the Albany-Fraser orogen consists of two main orebodies, Nova and Bollinger, hosted by the same tube-shaped intrusion but having distinctly different Ni tenors of around 6.5 and 4.8 wt %, respectively. Nova is also higher in Pd, but Cu and Pt tenors are similar. Both deposits have very low PGE tenors, with average Pd concentrations of 110 ppb in massive sulfide at Bollinger and 136 ppb at Nova. The Nova and Bollinger orebodies show relatively little internal differentiation overall on deposit scale but show strong differentiation into chalcopyrite-rich and chalcopyrite-poor regions at a meter scale. This differentiation is more prevalent at Nova, where massive sulfide-filled vein arrays are more extensively developed, and in massive ores, particularly veins, than in net-textured ores. Net-textured and disseminated ores have on average Ni and Cu grades and tenors similar to those of massive, semimassive, and breccia ores in the same orebody but a smaller range of variation, largely due to a more limited extent of sulfide liquid fractionation and higher average concentrations of Pt and Pd than adjacent massive ores. Unusually for differentiated magmatic sulfides, there is no systematic positive correlation between Pt, Pd, and Cu. A partial explanation for the lack of a Pd-Cu correlation is that Pd was partitioned into peritectic pentlandite in the middle stages of sulfide liquid solidification. This explanation is not applicable to Pt, as Pt characteristically forms its own phases rather than residing in base metal sulfides. PGE tenors are very low in both orebodies, very similar to those observed in other Ni-Cu-Co sulfide ores in orogenic settings, notably the Savannah and Savannah North orebodies. This depletion is attributed to sulfide retention in the mantle source of the parent magmas rather than to previous fractional extraction of sulfide liquid in staging chambers or feeder networks. The higher Ni and Pd tenors at Nova are attributed to reworking and upgrading of precursor sulfide liquid originally deposited upstream at the Bollinger site. Replicate analyses of multiple jaw-crusher splits returned highly variable Pt and Au assays but much smaller relative errors in the other PGEs. The poor Pt and Au reproducibilities are attributed to nugget effects, explicable by much of the Pt and Au in the samples being present in sparse Pt- and Au-rich grains. This is principally true for Pt in massive rather than disseminated ores, accounting for a strong contrast in the distribution of Pt/Pd ratios between the two ore types. Numerical simulation suggests that Pt is predominantly resident in Pt-rich platinum group minerals with grain diameters of 100 μm or more and that at the low (<100 ppb) concentrations in these ores, this results in most assays significantly underreporting Pt. This is likely to be true in other low-PGE ores, such that apparent negative Pt anomalies in massive ores may in such cases be attributable to sampling artifacts.

Genesis of sulfide vein mineralization at the Sakatti Ni-Cu-PGE deposit, Finland

2021 ◽  
Vol 59 (6) ◽  
pp. 1485-1510
Author(s):  
Fabian Fröhlich ◽  
Janne Siikaluoma ◽  
Inga Osbahr ◽  
Jens Gutzmer
Keyword(s):  
Solid Solution ◽  
Base Metal ◽  
Platinum Group Element ◽  
Group Element ◽  
Sulfide Liquid ◽  
Intermediate Solid Solution ◽  
Platinum Group Minerals ◽  
Magmatic Sulfide ◽  
Platinum Group ◽  
Residual Melt

ABSTRACT The Sakatti Ni-Cu-platinum-group element deposit is situated in northern Finland and comprises massive, disseminated, and vein sulfide mineralization. A stockwork is formed by chalcopyrite-rich sulfide veins, which contain exceptionally high platinum-group elements and Au grades. The mineralogy and geochemistry of this stockwork zone ore is documented in this investigation. The results are used to develop the first robust genetic concept and its relationship to massive and disseminated mineralization of the Sakatti deposit. This model is similar to that proposed for many Cu-rich magmatic sulfide ores, most importantly the Cu-rich footwall veins described from the Sudbury Complex in Canada and the Cu-rich ore at Noril'sk-Talnakh in Russia. Detailed petrographic studies using a sample suite from exploration drill core intersecting vein-style mineralization revealed a classic magmatic sulfide assemblage of chalcopyrite ± pyrrhotite, pentlandite, and pyrite. More than 1000 platinum-group mineral grains belonging almost exclusively to the moncheite (PtTe2) – merenskyite (PdTe2) – melonite (NiTe2) solid solution series were identified in the studied samples. Notably, almost two thirds of the platinum-group element-bearing minerals consist of melonite. Some of the platinum-group minerals contain inclusions of Ag-rich gold (AgAu2) and muthmannite (AuAgTe2). Most of the platinum-group minerals occur as inclusions in chalcopyrite, although a few grains are located at base-metal sulfide grain boundaries and in fractures in base-metal sulfides. The whole-rock compositions of the stockwork veins are Cu-rich and are interpreted to represent a fractionated Cu-rich sulfide liquid enriched in Pt, Pd, Au, Ag, As, Bi, Pb, Se, Te, Zn, which separated from a monosulfide solid solution (mss). An intermediate solid solution (iss) solidified from the Cu-rich sulfide liquid, recrystallizing chalcopyrite at <550 °C. Simultaneously, small volumes of intercumulus residual melt contained mainly the precious metals, Bi, and Te due to their incompatibility in iss. Solitary and composite platinum-group minerals as well as Au-minerals crystallized first from the residual melt (<600 °C), followed by a succession of various Bi-, Ag-, and Pb-tellurides (∼540 °C), and finally sphalerite and galena. Melonite crystallized as mostly large, solitary grains exsolved directly from Ni-bearing intermediate solid solution (∼600 °C), shortly after the formation of moncheite and merenskyite from the residual melt. Finally, remobilization of the platinum-group minerals occurred at temperatures of <300 °C, as suggested by the presence of minor amounts of Cl-bearing minerals and ragged grain shapes.

Sulfide mineral chemistry and platinum-group minerals of the UG-2 chromitite in the northern limb of the Bushveld Igneous Complex, South Africa

2021 ◽  
Vol 59 (6) ◽  
pp. 1339-1362
Author(s):  
Malose M. Langa ◽  
Pedro J. Jugo ◽  
Matthew I. Leybourne ◽  
Danie F. Grobler
Keyword(s):  
Platinum Group Element ◽  
Mineral Chemistry ◽  
Sulfide Mineral ◽  
Sulfide Minerals ◽  
Group Element ◽  
Igneous Complex ◽  
Northern Limb ◽  
Platinum Group Minerals ◽  
Platinum Group ◽  
Bushveld Igneous Complex

ABSTRACT The UG-2 chromitite layer, with its elevated platinum-group element content, is a key marker horizon in the eastern and western limbs of the Bushveld Igneous Complex and the largest platinum-group element chromite-hosted resource of its kind in the world. In contrast, much less is known about its stratigraphic equivalent in the northern limb, the “UG-2 equivalent” (UG-2E) chromitite. Recent studies on chromite mineral chemistry show similarities between the UG-2 and sections of the UG-2E, but also that the UG-2E was partially contaminated by assimilation of local metasedimentary rocks. Here, we provide a detailed characterization of sulfide minerals and platinum-group minerals in a suite of samples from the UG-2E and compare the results with data obtained from a reference suite of samples from the UG-2. Results from petrographic observations, electron probe microanalysis, laser ablation-inductively coupled plasma-mass spectrometry, quantitative evaluation of materials by scanning electron microscopy, and δ34S isotopes show that: (1) sulfide minerals in the UG-2E and UG-2 consist mainly of pentlandite-chalcopyrite-pyrrhotite, but pyrrhotite is significantly more abundant in the UG-2E and almost absent in the UG-2; (2) iron contents in pentlandite from the UG-2E are significantly higher than in the UG-2; (3) platinum-group element contents within sulfide minerals are different between the two chromitites; (4) UG-2E platinum-group minerals are dominated by arsenides and bismuthotellurides, and by alloys and platinum-group element-sulfide minerals in the UG-2; (5) sulfide mineral chemistry and δ34S values indicate some crustal contamination of the UG-2E; and (6) sulfide mineral and secondary silicate mineral textures in both the UG-2E and UG-2 are indicative of minor, millimeter- to centimeter-scale, hydrothermal alteration. From our observations and results, we consider the UG-2E chromitite in the northern limb to be the equivalent to the UG-2 in the eastern and western limbs that has been contaminated by assimilation of Transvaal Supergroup footwall rocks during emplacement. The contamination resulted in UG-2E sulfide mineral elemental contents and platinum-group mineral types and abundances that are distinct from those of the UG-2 in the rest of the Bushveld.

scholarly journals Suitability of surficial media for Ni-Cu-PGE exploration in an established mining camp: a case study from the South Range of the Sudbury Igneous Complex, Canada

2021 ◽  
pp. geochem2021-051
Author(s):  
Sarah Hashmi ◽  
Matthew I. Leybourne ◽  
Stewart Hamilton ◽  
Daniel Layton-Matthews ◽  
M. Beth McClenaghan
Keyword(s):  
Anthropogenic Contamination ◽  
The South ◽  
Aqua Regia ◽  
Content Type ◽  
Igneous Complex ◽  
Sudbury Igneous Complex ◽  
Geochemical Study ◽  
Pge Mineralization ◽  
Supplementary Material

A geochemical study over the southwestern part of the South Range of the Sudbury Igneous Complex (SIC) was completed to assess the suitability of surficial media (humus, B-horizon soil and C-horizon soil) for delineating geochemical anomalies associated with Ni-Cu-PGE mineralization. Another objective was to test whether Na pyrophosphate can eliminate the effects of anthropogenic contamination in humus. Results of this study suggest that the natural geochemical signature of humus is strongly overprinted by anthropogenic contamination. Despite no indication of underlying or nearby mineralization, metal concentrations in humus samples by aqua regia collected downwind from smelting operations are higher compared to background, including up to 13 times higher for Pt, 12 times higher for Cu and 9 times higher for Ni. The high anthropogenic background masks the geogenic signal such that it is only apparent in humus samples collected in the vicinity of known Ni-Cu-PGE deposits. Results of this study also demonstrate that anthropogenically-derived atmospheric fallout also influences the upper B-horizon soil; however, lower B-horizon soil (at > 20 cm depth) and C-horizon soil (both developed in till) are not affected. Glacial dispersal from Ni-Cu-PGE mineralization is apparent in C-horizon till samples analyzed in this study. Compared to the background concentrations, the unaffected C-horizon till samples collected immediately down-ice of the low-sulfide, high precious metal (LSHPM) Vermilion Cu-Ni-PGE deposit are enriched over 20 times in Pt (203 ppb), Au (81 ppm) and Cu (963 ppm), and over 30 times in Ni (1283 ppm).Supplementary material:https://doi.org/10.6084/m9.figshare.c.5691080

scholarly journals Assessing the extent of local crust assimilation within the Flatreef, northern limb of the Bushveld Igneous Complex, using sulfur isotopes and trace element geochemistry

2020 ◽  
Author(s):  
Evan Keir-Sage ◽  
Matthew I. Leybourne ◽  
Pedro J. Jugo ◽  
Danie F. Grobler ◽  
Cédric C. Mayer
Keyword(s):  
Trace Element ◽  
Primitive Mantle ◽  
Trace Element Geochemistry ◽  
Isotopic Data ◽  
Igneous Complex ◽  
Merensky Reef ◽  
Northern Limb ◽  
Geochemical Parameters ◽  
Pge Mineralization ◽  
Bushveld Igneous Complex

Abstract The proximity to metasedimentary footwall rocks relative to platinum group element (PGE) mineralized intrusive rocks in the northern limb of the Bushveld Igneous Complex (BIC) has resulted in complex local contamination in the intrusions. To assess the extent of incorporation of non-magmatic material and its effects on PGE mineralization, major element, trace element, and S isotopic data were collected from drill core UMT094 on the Turfspruit farm, where core logging has shown that the mineralized Platreef, forming the Flatreef deposit, is located stratigraphically well above local sedimentary footwall rocks. The S isotopic data combined with whole rock geochemistry data (including CaO/Al2O3, (V/Ti)PM, (Ni/Cr)PM, S/Se, loss on ignition) were used to assess incorporation of a range of local footwall material. The δ34S data show a steady decrease from the footwall assimilation zone (δ34S typically + 8 to + 9‰, maximum 12‰) to near constant δ34S values (δ34S < + 4‰) below the main PGE reef. Similar values have been documented for the Merensky Reef in the eastern and western limbs of the BIC (δ34S ~ 0 to + 3.5‰). Other geochemical parameters, such as S/Se and CaO/Al2O3, also match the ranges documented for the Merensky Reef elsewhere in the BIC. In addition, parameters such as whole rock V/Ti, normalized to primitive mantle (V/Ti)PM, are shown to be useful indicators of contamination and the type of contaminant with 1 < (V/Ti)PM < 2 for uncontaminated magmatic units; [V/Ti]pm > 2 for shale assimilation; and [V/Ti]pm < 1 for carbonate assimilation. The results suggest that the main PGE mineralization in the Flatreef deposit formed without significant in situ contamination and that the primary mechanism of PGE mineralization in the Platreef at Turfspruit was no different than the mechanism that generated the Merensky Reef in the eastern and western limbs of the BIC.

scholarly journals Introduction to the special issue on the Flatreef PGE-Ni-Cu deposit, northern limb of the Bushveld Igneous Complex

2020 ◽  
Author(s):  
Wolfgang D. Maier ◽  
Marina Yudovskaya ◽  
Pedro Jugo
Keyword(s):  
Ore Deposits ◽  
Special Issue ◽  
Ore Formation ◽  
Igneous Complex ◽  
Northern Limb ◽  
Pge Mineralization ◽  
World Class ◽  
Bushveld Igneous Complex ◽  
Mine Development ◽  
Host Rocks

AbstractMore than 30 years ago, Cox and Singer (1986) suggested that magmatic platinum-group element (PGE)-Ni-Cu deposits are amongst the best understood of ore deposits, yet the origin of PGE mineralization in the Bushveld Igneous Complex (BIC) remains controversial after a century of study. In the northern limb of the BIC, the unravelling of ore formation proved particularly difficult due to relatively poor outcrop, which is typically affected by contamination of the intruding magmas with the host rocks and expressed in the form of abundant xenoliths, footwall rafts and disturbance of magmatic stratigraphy. In this thematic issue, we present contributions on the Flatreef, a recently discovered world-class PGE-Ni-Cu deposit constituting a downdip extension of the mineralized unit of the Platreef of the northern limb. Two deep shafts are currently being sunk, making the Flatreef one of the most significant new mine development on the Bushveld in several decades.

The Samapleu mafic-ultramafic intrusion and its Ni-Cu-PGE mineralization: an Eburnean (2.09 Ga) feeder dyke to the Yacouba layered complex (Man Archean craton, western Ivory Coast)

2014 ◽  
Vol 185 (6) ◽  
pp. 393-411 ◽  
Author(s):  
Franck Gouedji ◽  
Christian Picard ◽  
Yacouba Coulibaly ◽  
Marc-Antoine Audet ◽  
Thierry Auge ◽  
...  
Keyword(s):  
Hybrid Zone ◽  
Ivory Coast ◽  
Country Rock ◽  
Parental Magma ◽  
Massive Sulfide ◽  
Contact Metamorphism ◽  
Sulfide Deposit ◽  
Sulfide Liquid ◽  
Melt Composition ◽  
Layered Complex

Abstract The Yacouba layered complex intrudes the Archean (3.5–2.7 Ga) Kenema-Man craton in the Samapleu-Yorodougou area, western Ivory Coast. In Samapleu area, the complex was recognized in drill holes at three locations: Samapleu Main (SM); Samapleu Extension 1 (E1) and Yorodougou (Yo). It comprises websterites, peridotites and gabbro-norites arranged symmetrically with mafic layers at the center and ultramafic layers at both margins. The complex is inclined at 70–80° to the SE. The thickness of individual layers varies from 2 to 60 m and the total thickness is 120 to 200 m. At the E1 site, the complex extends to depths &gt; 500 m. Contacts with the country rock gneiss are characterized by a hybrid zone that is a few meters thick and composed of plagioclase-orthopyroxene bearing metabasites, and locally (E1 site) a metamorphic assemblage of sapphirine-cordierite-sillimanite-spinel ± rutile. This assemblage is attributed to contact metamorphism during intrusion of the complex in the lower crust at a depth of about 25 km. Zircons in country rock gneisses and granulites, as well as in the hybrid facies, yield Archean ages of ~ 2.78 Ga, similar to ages reported in the Man craton. Rutiles in the hybrid zone give a U-Pb age of 2.09 Ga, which is interpreted as the age of contact metamorphism and emplacement of the intrusion. The Samapleu Main and Samapleu Extension 1 sites contain Ni and Cu sulfide deposit with reserves estimated as more than 40 million tons grading 0.25% Ni and 0.22% Cu (Sama Nickel-CI, August 2013). The Ni-Cu mineralization is composed of pentlandite, chalcopyrite, pyrrhotite and rare pyrite, which is disseminated mainly in pyroxenite or occurs as subvertical and semi-massive to massive sulfide veins. The sulfide textures range from matrix ore, net-textured, droplets or breccia textures. Zones enriched in PGM, particularly Pd, are associated with the sulfides and several chromite bands are also present. These observations suggest that an immiscible sulfide liquid formed from a parental silicate liquid and percolated through the crystal pile. The parental melt composition, determined using the Chai and Naldrett [1992] method, has a SiO2-rich mafic composition with 53% SiO2 and 10% MgO. This result, the presence of the hybrid zone, and the trace-element signature determined using the Bedard [1994] method, suggest a mantle-derived basaltic parental magma that had assimilated abundant continental crust. These observations indicate that Samapleu intrusion corresponds to a magmatic conduit of the Yacouba complex as at Jinchuan (China), Voisey’s bay (Canada), Kabanga (Tanzania) or Nkomati (South Africa).

Concentrations of Te, As, Bi, Sb (TABS) and Se in the Marginal Zone of the Bushveld Complex: evidence for crustal contamination and the nature of the magma that formed the Merensky Reef

2020 ◽  
Author(s):  
Eduardo Mansur ◽  
Sarah-Jane Barnes
Keyword(s):  
Marginal Zone ◽  
Bushveld Complex ◽  
Crustal Contamination ◽  
Sulfide Minerals ◽  
Sulfide Liquid ◽  
Liquid Component ◽  
Merensky Reef ◽  
Chalcophile Elements ◽  
Magmatic Sulfide ◽  
Primary Magmas

&lt;p&gt;The association of platinum-group elements (PGE) and the chalcophile elements Te, As, Bi, Sb and Sn (TABS) has been documented in several magmatic sulfide deposits. These groups of elements are either hosted within sulfide minerals, or combine to form discrete platinum-group minerals (PGM) associated with sulfide minerals. However, the concentration of TABS in parental magmas from which magmatic sulfide deposits formed was still missing. This study presents the distribution of TABS and Se in B-1, B-2 and B-3 rocks of the Marginal Zone of the Bushveld Complex. These rocks have been proposed as representative of the parental liquids from which the Bushveld Complex crystallized, thus allowing us to assess the concentration of Se and TABS in the liquids from which some of the largest PGE deposits in the world have formed. Concentrations of As and Sb in the initial Bushveld liquid (B-1) are significantly higher than in primary magmas, whereas the Se and TABS of later magmas (B-2 and B-3) are similar to primary magmas. We attribute the difference due upper crustal contamination of the B-1 magma, whereas the B-2 and B-3 magmas were most likely contaminated with a plagioclase-rich residuum formed upon the partial melting of the upper crust. Moreover, we modeled the concentrations of the TABS in the Merensky Reef using a mixture of two of the magma types present in the Marginal Zone (the B-1 and B-2) as the initial silicate liquid. The modeled concentrations closely resemble the measured values obtained for a section across the Merensky Reef at the Impala mine. This supports the B-1 and B-2 mixture as an appropriate initial liquid for the crystallization of the Merensky Reef. The modeling also shows that the distributions of Se, Te and Bi across the Merensky Reef are controlled by the sulfide liquid component. In contrast, As and Sb distributions are influenced both by the amount of silicate melt component in the cumulates and the sulfide liquid component. This is because Se, Te and Bi are moderately to strongly chalcophile elements, but As and Sb are only slightly chalcophile elements. Consequently, the effect of crustal contamination for elements with high partition coefficients between sulfide and silicate liquid (Te, Bi and Se) is obscured by the interaction of sulfides with a large volume of silicate magma. Therefore, the concentrations of these elements are higher in samples with greater proportions of sulfide minerals. In contrast, for elements with lower partition coefficients (As and Sb), the whole-rock concentrations are not upgraded by the presence of sulfide minerals, and thus the effect of crustal contamination can be more readily assessed.&lt;/p&gt;

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