Constraining olivine abundance and water content of the mantle at the 410-km discontinuity from the elasticity of olivine and wadsleyite
2019
EARTH AND PLANETARY SCIENCE LETTERS
DOI
10.1016/j.epsl.2019.04.018
Velocity and density jumps across the 410-km seismic discontinuity generally indicate olivine contents of similar to 30 to 50 vol.% on the basis of the elastic properties of anhydrous olivine and wadsleyite, which is considerably less than the similar to 60% olivine in the widely accepted pyrolite model for the upper mantle. A possible explanation for this discrepancy is that water dissolved in olivine and wadsleyite affects their elastic properties in ways that can reconcile the pyrolitic model with seismic observations. In order to more fully constrain the olivine content of the upper mantle near the 410-km discontinuity, and to place constraints on the mantle water content at this depth, we determined the full elasticity of hydrous wadsleyite at the P-T conditions of the discontinuity based on density functional theory calculations. Together with previous determinations for the effect of water on olivine elasticity, we simultaneously modeled the density and seismic velocity jumps (Delta(rho), Delta V-p, Delta V-S) across the olivine-wadsleyite transition. Our models allow for several scenarios that can well reproduce the density and seismic velocity jumps across the 410-km discontinuity when compared to globally averaged seismic models. When the water content of olivine and wadsleyite is assumed to be equal as in a simple binary system, our modeling indicates a best fit for low water contents (<0.1 wt.%) with an olivine proportion of similar to 50%, suggesting a relatively dry, non-pyrolitic mantle at depths of the 410-km discontinuity. However, our modeling can be reconciled with a pyrolitic mantle if the water content in wadsleyite is similar to 0.9 wt.% and that in olivine is at its storage capacity of similar to 500-1500 ppm. The result would be consistent with a hydrous melt phase produced at depths just above the phase transition. (C) 2019 Elsevier B.V. All rights reserved.