Abstract
The partition of Mn and Mg between coexisting synthetic olivine, orthopyroxene and Ca-rich clinopyroxene was studied. The apparent equilibrium constant for the partition of Mn and Mg between olivine and orthopyroxene, K′ (=(Mn/Mg) Ol (Mg/Mn) Opx), was measured under the conditions of 1200 °C, 30 kb; 1000 °C, 30 kb; and 1050 °C, 0 kb. The pressure dependence of ln K′ was found to be −0.0040/kb (±0.0010) at 1000 °C in the composition range around Mn/(Mn+Mg) = 0.05. This value agrees quite well with the theoretical value, −0.0043/kb, based on unit cell parameter data. Composition and temperature dependences of K′ were also observed. In the systems containing Ca-rich clinopyroxene, the reaction rate was so small that no equilibrated samples were obtained. The formation condition of a garnet peridotite xenolith in South African kimberlite was estimated by thermodynamic analysis of the partition of MnMg and CoMg between olivine and orthopyroxene, assuming the binary regular solution model. It was concluded that the garnet peridotite xenolith had been formed at a temperature of about 100 °C lower and at a pressure of about 60 kb higher than the Itinomegata spinel lherzolite nodule. Unit cell parameters of synthetic MnMg olivine and orthopyroxene solid solutions are reported in the Appendix.
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