Incorporation of tetrahedral ferric iron into hydrous ringwoodite

Author:

Thomson Andrew R.12,Piltz Ross O.3,Crichton Wilson A.2,Cerantola Valerio34,Ezad Isra S.15,Dobson David P.16,Wood Ian G.1,Brodholt John P.17

Affiliation:

1. Department of Earth Sciences, University College London, London WC1E 6BT, U.K.

2. ESRF, The European Synchrotron, 38043 Grenoble, France

3. Australian Centre for Neutron Scattering, Lucas Heights, New South Wales 2234, Australia

4. European XFEL, Holzkoppel 4, 22869 Schenefeld, Germany

5. Department of Earth and Environmental Sciences, Macquarie University, Sydney, New South Wales 2109, Australia

6. Bayeriches Geoinstitut, University of Bayreuth, 95440 Bayreuth, Germany

7. Centre for Earth Evolution and Dynamics, University of Oslo, N-0316 Oslo, Norway

Abstract

Abstract Hydrous Fo91 ringwoodite crystals were synthesized at 20 GPa and high-temperature conditions using a multi-anvil press. Recovered crystals were analyzed using electron microprobe analysis, Raman spectroscopy, infrared spectroscopy, synchrotron Mössbauer spectroscopy, single-crystal X-ray diffraction, and single-crystal Laue neutron diffraction, to carefully characterize the chemistry and crystallography of the samples. Analysis of the combined data sets provides evidence for the presence of tetrahedrally coordinated ferric iron and multiple hydrogen incorporation mechanisms within these blue-colored iron-bearing ringwoodite crystals. Tetrahedral ferric iron is coupled with cation disorder of silicon onto the octahedrally coordinated site. Cation disorder in mantle ringwoodite minerals may be promoted in the presence of water, which could have implications for current models of seismic velocities within the transition zone. Additionally, the presence of tetrahedrally coordinated ferric iron may cause the blue color of many ringwoodite and other high-pressure crystals.

Publisher

Mineralogical Society of America

Subject

Geochemistry and Petrology,Geophysics

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