Abstract

Platinum group elements are invaluable tracers for planetary accretion and differentiation and the formation of PGE sulfide deposits. Previous laboratory determinations of the sulfide liquid–basaltic melt partition coefficients of PGE ({D}_{PGE}^{SL/SM}) yielded values of 102–109, and values of >105 have been accepted by the geochemical and cosmochemical society. Here we perform measurements of {D}_{Pt,,Pd}^{SL/SM} at 1 GPa and 1,400 °C, and find that {D}_{Pt,,Pd}^{SL/SM} increase respectively from 3,500 to 3.5 × 105 and 1,800 to 7 × 105, as the Pt and Pd concentration in the sulfide liquid increases from 60 to 21,000 ppm and 26 to 7,000 ppm, respectively, implying non-Henrian behavior of the Pt and Pd partitioning. The use of {D}_{Pt,,Pd}^{SL/SM} values of 2,000–6,000 well explains the Pt and Pd systematics of Earth’s mantle peridotites and mid-ocean ridge basalts. Our findings suggest that the behavior of PGE needs to be reevaluated when using them to trace planetary magmatic processes.

Highlights

  • Platinum group elements are invaluable tracers for planetary accretion and differentiation and the formation of PGE sulfide deposits

  • We find that DPSLt;=PSdM increase with increasing CSPLt; Pd, and the use of DPSLt;=PSdM values of < 104, which correspond to the CSPLt; Pd in Earth’s magmatic systems, can well explain the observed Pt and Pd systematics of Earth’s mantle peridotites and mid-ocean ridge basalts (MORB)

  • Pt and Pd partitioning between sulfide liquid and basaltic melt

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Summary

Introduction

Platinum group elements are invaluable tracers for planetary accretion and differentiation and the formation of PGE sulfide deposits. Experimental determinations on the partition coefficients of PGE between sulfide liquid and silicate (basaltic) melt (DPSLG=ESM) have yielded widely discrepant results, with DPSLG=ESM values ranging from 102 to

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