Water partitioning between nominally anhydrous minerals in the MgO-SiO2-H2O system up to 24 GPa: implications for the distribution of water in the Earth's mantle
N. Bolfan-casanova et al., Water partitioning between nominally anhydrous minerals in the MgO-SiO2-H2O system up to 24 GPa: implications for the distribution of water in the Earth's mantle, EARTH PLAN, 182(3-4), 2000, pp. 209-221
Multi-anvil experiments have been conducted in the MgO-SiO2-H2O system at p
ressures of 15-24 CPa and temperatures of 1200-1600 degreesC to investigate
the partitioning of water between mantle phases. The water contents were o
btained from Fourier transform infrared spectroscopy on doubly polished and
clear crystals. Most of the mineral phases coexisted with a hydrous melt.
The results show that among all magnesium silicate phases (1) MgSiO3-perovs
kite is the only phase which does not dissolve a detectable amount of water
and (2) the high-pressure polymorphs of Mg2SiO4, wadsleyite and ringwoodit
e, dissolve about one order of magnitude more water than the polymorphs of
MgSiO3 (clinoenstatite, majorite and akimotoite). The following partition c
oefficients of water were measured: D-wadsleyite/clinoenstatite = 3.8 at 15
GPa and 1300 degreesC, D-ringwoodite/akimotoite = 21 at 19 GPa and 1300 de
greesC, D-akimotoite/perovskite >> 1 at 24 GPa and 1600 degreesC, and D-per
ielase/perovskite > 1 at 24 GPa and 1500 degreesC. These results suggest th
at most of the water in the Earth's mantle is partitioned in the transition
zone. (C) 2000 Elsevier Science B.V. Ail rights reserved.