Abstract

Mechanisms and kinetics of exsolution of majoritic garnet from Ca–Tschermak-rich clinopyroxene were examined at 14.0–15.6 GPa, 1250–1590 °C, and H 2O-undersaturated conditions (800–1170 wt. ppm H 2O) by time-resolved in situ synchrotron X-ray diffraction measurements. Textural observations of recovered samples revealed that majoritic garnet had exsolved along the grain boundaries of parent clinopyroxene. Analyses of the kinetic data obtained indicate that exsolved majoritic garnet grew by diffusion-controlled growth, and the growth kinetics can be described by k 2 (m 2/s) = 7.4 × 10 −5 exp[−389(kJ mol −1)/ RT]. The exsolution of majoritic garnet from clinopyroxene would be kinetically inhibited at temperatures below ∼800 °C in geological time scales (10 5–10 6 years) when the parent grain size is larger than 1 mm. We constructed possible phase relations of subducting mid-ocean ridge basalt (MORB) taking the exsolution kinetics into consideration. When the effect of reaction kinetics is considered, the density contrast between the MORB component of a subducting slab and surrounding mantle becomes significantly reduced relative to that calculated for the equilibrium MORB assemblage.

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