Synthesis of inverse ringwoodite sheds light on the subduction history of Tibetan ophiolites

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作者
Luca Bindi
William L. Griffin
Wendy R. Panero
Ekaterina Sirotkina
Andrey Bobrov
Tetsuo Irifune
机构
[1] Università di Firenze,Dipartimento di Scienze della Terra
[2] CNR-Istituto di Geoscienze e Greorisorse,ARC Centre of Excellence for Core to Crust Fluid Systems and GEMOC, Department of Earth and Planetary Sciences
[3] Macquarie University,School of Earth Sciences
[4] Ohio State University,Department of Petrology, Geological Faculty
[5] Columbus,Geodynamics Research Center
[6] Vernadsky Institute of Geochemistry and Analytical Chemistry of Russian Academy of Sciences,undefined
[7] Moscow State University,undefined
[8] Institute of Experimental Mineralogy of Russian Academy of Sciences,undefined
[9] Ehime University,undefined
[10] Earth-Life Science Institute,undefined
[11] Tokyo Institute of Technology,undefined
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摘要
Tibetan ophiolites are shallow mantle material and crustal slabs that were subducted as deep as the mantle transition zone, a conclusion supported by the discovery of high-pressure phases like inverse ringwoodite in these sequences. Ringwoodite, Mg2SiO4, exhibits the normal spinel structure, with Mg in the octahedral A site and Si in the tetrahedral B site. Through A and B site-disorder, the inverse spinel has four-coordinated A cations and the six-coordinated site hosts a mixture of A and B cations. This process affects the density and impedance contrasts across the boundaries in the transition zone and seismic-wave velocities in this portion of the Earth. We report the first synthesis at high pressure (20 GPa) and high temperature (1600 °C) of a Cr-bearing ringwoodite with a completely inverse-spinel structure. Chemical, structural, and computational analysis confirm the stability of inverse ringwoodite and add further constraints to the subduction history of the Luobusa peridotite of the Tibetan ophiolites.
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