V012-02
Partitioning of chalcophile and Highly Siderophile Elements (HSEs) between sulfide and carbonated melts – Implications for HSE systematics of kimberlites and carbonatites
Abstract:
Here we experimentally determine the partitioning of HSEs and ChEs (Ni, Co, Mo, Os, Ru, Pd, Pt and Re) between sulfide melt and two type of carbonated melts (high CO2 and low CO2) at a pressure (P) of 3 GPa and temperatures (T) of 1300-1600 °C in graphite capsules. All experiments produced quenched Fe-sulfide melt blobs + carbonated silicate melt matrix. Concentrations of major elements were measured using electron microprobe and HSEs and ChEs are measured using LA-ICP-MS. We find that all the elements measured are compatible in the sulfide melt to varying degrees and their Dsulfide/carbonated melt sequence is Mo < Co < Ni < Re < Pt ≤ Pd < Ru ≤ Os, yet the D values for HSEs are lower than those in sulfide-silicate melt systems. Calculating bulk D for carbonated peridotite using our measured D values, we model the HSE contents of mantle derived low-degree partial melts and compare the primitive mantle normalized HSE patterns of our model melts with natural kimberlites and carbonatites. To explain the difference between our model low-degree melts and natural carbonatites and kimberlites, we calculate proportions of sub-continental lithospheric mantle (SCLM) xenolith detritus for kimberlite and carbonatite samples from Finland, South Africa, Canada, and North China by using mass balance calculations based on Ru concentration in the primary carbonated melt and the SCLM xenolith. Our calculations show that detritus proportion in natural kimberlites are 2-28% for Finland, 25-40% for South Africa, and 6-16% for Canada, which are comparable to modelled calculations by previous studies using various other proxies [1].
[1] Tappe et al., 2017, Chem. Geol.