Experimentally determined partition coefficients for minor and trace elements in peridotite minerals and carbonatitic melt, and their relevance to natural carbonatites
Experimentally determined partition coefficients for minor and trace elements in peridotite minerals and carbonatitic melt, and their relevance to natural carbonatites (in Eighth international symposium on Experimental mineralogy, petrology and geochemistry, Anonymous)
European Journal of Mineralogy (October 2001) 13 (5): 815-827
- alkaline earth metals
- amphibole group
- basaltic composition
- carbonatites
- chain silicates
- chemical composition
- clinopyroxene
- concentration
- electron probe data
- enrichment
- equilibrium
- experimental studies
- garnet group
- geochemistry
- high pressure
- high temperature
- ICP mass spectra
- igneous rocks
- laser ablation
- laser methods
- magmas
- mantle
- mass spectra
- melts
- metals
- mineral composition
- minor elements
- nesosilicates
- orthosilicates
- partial melting
- partition coefficients
- peridotites
- plutonic rocks
- pressure
- pyroxene group
- silicates
- spectra
- temperature
- trace elements
- ultramafics
- magnesiocabonatitic melts
A laser ablation microprobe coupled to an ICP-MS was used to determine K, Rb, Cs, Sr, Ba, Ti, Zr, Hf, Nb, La, Ce, Ho, Yb and Lu in garnet, clinopyroxene, amphibole and magnesiocarbonatitic melt produced at 1050 degrees C and 2.5 GPa from a synthetic composition designed to simulate the melting of natural peridotite. Crystal/melt partition coefficients were then used to calculate minor and trace element contents in a hypothetical carbonatitic melt equilibrated with a garnet-amphibole lherzolite of primitive mantle composition. The melt is strongly enriched in alkaline earths and REE relative to HFSE and alkalis, and plots within the compositional range of natural carbonatites. The fractionation of alkaline earths and REE from alkalis and HFSE, however, is usually larger in natural carbonatites than for the calculated composition. Processes in addition to peridotite melting (such as crystal fractionation, wall rock reactions and variations in source chemistry) are needed to fully account for the minor and trace element characteristics of carbonatites.