Abstract

This paper reviews a database of about 1500 published and 1000 unpublished microprobe analyses of platinum-group minerals (PGM) from chromite deposits associated with ophiolites and Alaskan-type complexes of the Urals. Composition, texture, and paragenesis of unaltered PGM enclosed in fresh chromitite of the ophiolites indicate that the PGM formed by a sequence of crystallization events before, during, and probably after primary chromite precipitation. The most important controlling factors are sulfur fugacity and temperature. Laurite and Os–Ir–Ru alloys are pristine liquidus phases crystallized at high temperature and low sulfur fugacity: they were trapped in the chromite as solid particles. Oxygen thermobarometry supports that several chromitites underwent compositional equilibration down to 700 °C involving increase of the Fe3/Fe2 ratio. These chromitites contain a great number of PGM including—besides laurite and alloys—erlichmanite, Ir–Ni–sulfides, and Ir–Ru sulfarsenides formed by increasing sulfur fugacity. Correlation with chromite composition suggests that the latest stage of PGM crystallization might have occurred in the subsolidus. If platinum-group elements (PGE) were still present in solid chromite as dispersed atomic clusters, they could easily convert into discrete PGM inclusions splitting off the chromite during its re-crystallization under slow cooling-rate. The presence of primary PGM inclusions in fresh chromitite of the Alaskan-type complexes is restricted to ore bodies crystallized in equilibrium with the host dunite. The predominance of Pt–Fe alloys over sulfides is a strong indication for low sulfur fugacity, thereby early crystallization of laurite is observed only in one deposit. In most cases, Pt–Fe alloys crystallized and were trapped in chromite between 1300 and 1050 °C. On-cooling equilibration to ~900 °C may produce lamellar unmixing of different Pt–Fe phases and osmium. Precipitation of the Pt–Fe alloys locally is followed by an increase of sulfur fugacity leading to crystallize erlichmanite and Ir–Rh–Ni–Cu sulfides, occurring as epitaxic overgrowth on the alloy. There is evidence that the system moved quickly into the stabilization field of Pt–Fe alloys by an increase of the oxygen fugacity marked by an increase of the magnetite component in the chromite. In summary, the data support that most of the primary PGM inclusions in the chromitites of the Urals formed in situ, as part of the chromite precipitation event. However, in certain ophiolitic chromitites undergoing annealing conditions, there is evidence for subsolidus crystallization of discrete PGM from PGE atomic-clusters occurring in the chromite. This mechanism of formation does not require a true solid solution of PGE in the chromite structure.

Highlights

  • Ever since pioneer geochemical surveys of ultramafic rocks [1,2,3,4,5,6,7,8,9,10,11,12,13], chromitite has been recognized as a potential concentrator of platinum-group elements (PGE = Os, Ir, Ru, Rh, Pt, Pd)

  • Most authors have divided the platinum-group minerals (PGM) into two genetically distinct categories, based on their textural relations: (1) the “primary” PGM occurring enclosed in fresh chromite far from cracks and alteration zones, and (2) the “secondary” PGM being invariably associated with low-temperature assemblages, either included in the ferrianchromite rim of chromite grains, or in the interstitial silicate matrix. In this overview we have focused our attention on the paragenetic characters of the primary PGM occurring enclosed in fresh chromite thereby reflecting high temperature conditions of formation, having been preserved from low-temperature alteration

  • The review based on examination of more than 2500 analyses of PGM associated with ophiolitic and Alaskan-type chromitites of the Urals reveals that mineralogy of PGM crystallizing at high temperature is controlled by: (1) the nature of the parent melt and relative concentrations of PGE; (2) the presence of melt-soluble clusters of PGE in the parent melt; and (3) by the chemical-physical conditions such as temperature, sulfur- and oxygen-fucagity, prevailing during their precipitation

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Summary

Introduction

Mineralogical investigations carried out between 1996 and 2016 have described in detail the diverse PGM assemblages of the chromitites, thereby establishing a close consistency between the geochemistry and mineralogy of the PGE [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45] The results of these studies, did not lead to a conclusive model able to adequately explain the primary origin of PGM inclusions in the chromite. Comparison of PGE-PGM data with chromite composition allows us to explore the possible correlation between the type of PGM mineralization and conditions invoked for the precipitation of chromite at high magmatic Minerals 2018, 8, 379 temperature, or the influence of chromite on-cooling equilibration in the subsolidus stage

Geological and Provenance microprobeSetting analyses of Sample
Geological
The paragenesisofand composition of these
Back-scattered
Relationships with Chromite Composition
Discarding unrealistic
Primary
The Role of Oxygen Fugacity and Temperature
Thermodynamic Conditions for Precipitation of Primary Pt–Fe Alloys
Findings
Conclusions
Full Text
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