UPGRADING OF MAGMATIC SULFIDES, REVISITED

2020 ◽  
Vol 115 (8) ◽  
pp. 1827-1833
Author(s):  
James E. Mungall ◽  
M. Christopher Jenkins ◽  
Samuel J. Robb ◽  
Zhuosen Yao ◽  
James M. Brenan

Abstract There has been vigorous debate for several decades about whether the extreme enrichments of platinum group elements (PGEs) in some magmatic sulfide deposits could have resulted from simple equilibration of sulfide liquid with silicate melt. Key examples include the Ni-Cu-Pd mineralization in the Norilsk mining camp, the UG2 and Merensky reef Pt-Pd deposits in the Bushveld Complex, the Pd-rich J-M reef of the Stillwater Complex, and the Skaergaard Pd-Au mineralization. It was argued historically that the observed PGE tenors in these latter deposits are too high to be consistent with simple equilibration of sulfide and silicate melt. A commonly cited mechanism for increasing PGE tenor in magmatic sulfide is the upgrading of initially low tenor sulfide by allowing a small volume of sulfide to react with successive batches of fresh, previously undepleted silicate magma. Here we review several previous models for sulfide upgrading in light of recent changes in accepted values of the partition coefficients governing PGE exchange between sulfide and silicate, and we critically examine the physical scenarios implicit in each previous model. We show that, although sulfide upgrading may occur in natural settings such as fractional melting of the mantle, during the formation of sulfide accumulations from magmas it is unlikely to have effects that can be distinguished from simple one-stage batch equilibration. Even the most PGE-rich deposits currently known have compositions that can easily be accounted for by the simple one-stage batch process, with the possible exception of the Skaergaard Pd mineralization. It is generally not possible to use the measured composition of accumulations of magmatic sulfide to infer that sulfide upgrading has or has not occurred.

Author(s):  
Stephen J. Barnes ◽  
Chris Ryan ◽  
Gareth Moorhead ◽  
Rais Latypov ◽  
Wolfgang D. Maier ◽  
...  

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.


2021 ◽  
Vol 497 (1) ◽  
pp. 206-210
Author(s):  
N. S. Gorbachev ◽  
Yu. B. Shapovalov ◽  
A. V. Kostyuk ◽  
P. N. Gorbachev ◽  
A. N. Nekrasov ◽  
...  

2020 ◽  
Vol 536 ◽  
pp. 116162 ◽  
Author(s):  
Zhenjiang Wang ◽  
Zhenmin Jin ◽  
James E. Mungall ◽  
Xianghui Xiao
Keyword(s):  

2020 ◽  
Vol 55 (8) ◽  
pp. 1515-1534
Author(s):  
M. Moilanen ◽  
E. Hanski ◽  
J. Konnunaho ◽  
T. Törmänen ◽  
S.-H. Yang ◽  
...  

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.


2020 ◽  
Vol 115 (8) ◽  
pp. 1799-1826
Author(s):  
M. Christopher Jenkins ◽  
James E. Mungall ◽  
Michael L. Zientek ◽  
Paul Holick ◽  
Kevin Butak

Abstract In this contribution, we analyze 30 years of mine development data and quantitatively identify the processes that control the grade and tenor of the mineralized rock. An assay database of more than 60,000 samples was used to examine variations in ore grade and tenor of the sulfide mineralization in the J-M reef horizon of the Stillwater Complex along the strike and down the dip of the deposit in the area of the Stillwater mine. We compare these results with data from the East Boulder mine and whole-rock lithogeochemistry of samples collected along the entire strike length of the complex. We find significant variation in the composition of the reef sulfides in different spatial domains of the Stillwater mine area and between the Stillwater and East Boulder mines. Most of the variation in the grade and tenor can be explained by a variation in the mass of silicate magma with which the sulfide liquid equilibrated (i.e., R factor); however, geochemical and textural evidence suggests that parts of the reef may have experienced significant S loss following initial sulfide melt segregation. Some variability in the reef tenor and grade can be attributed to variable amounts of sulfur loss due to low-temperature hydrothermal fluids and the overestimation or underestimation of metal concentrations in reef assays due to the nugget effect. Furthermore, we address the Pd/Pt ratio of the reef samples and suggest that the lower solubility of Pt in the parental silicate melt may have caused the crystallization and removal of Pt alloys at some point before the melt reached sulfide saturation and Pt could partition into the sulfide liquid. This disparity between the prior evolution of Pt and Pd in the silicate melt resulted in the observed Pd/Pt ratio of ~3.65 across all areas of the reef—a value significantly larger than anticipated for primitive mantle-derived magmas.


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