Abstract
The phase equilibria on the join MgSiO3–MnSiO3 were determined experimentally in the pressure – temperature range 1–25 kb and 600–1150°C. The following phase assemblages were encountered from MgSiO3 side to MnSiO3 component, the single phase of orthopyroxeneSS, orthopyroxene + clinopyroxene, clinopyroxeneSS (kanoite), clinopyroxene + pyroxmangite, pyroxmangiteSS, pyroxmangite + rhodonite, and rhodoniteSS. Below 700°C, olivine is present and the following two fields are encountered; olivine + clinopyroxene + quartz and olivine + quartz + pyroxmangite.
Rhodonite has a limited field (95 mol% MnSiO3) for all pressures and temperatures. Solubility of MgSiO3 in pyroxmangite increases linearly with increasing temperature, at least below 10 kb, and that of MnSiO3 in orthopyroxene increases with increasing pressure. Unit cell constants of the pyroxenes increase linearly with increasing MnSiO3 content. The clinopyroxene is indexed in the space group P21/c, analogous to the natural kanoite. The miscibility gaps observed in our study are consistent with those in natural samples from Tatehira mine, Hokkaido, Japan.