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AGU: Geophysical Research Letters

 

Keywords

  • carbon
  • mantle
  • ab initio

Index Terms

  • Mineralogy and Petrology: Reactions and phase equilibria
  • Mineral Physics: High-pressure behavior
  • Mineral Physics: Physical thermodynamics
  • Mineralogy and Petrology: Mineral and crystal chemistry
  • Mineralogy and Petrology: Mantle processes

Abstract

GEOPHYSICAL RESEARCH LETTERS, VOL. 35, L14307, 5 PP., 2008
doi:10.1029/2008GL034442

Mantle-wide sequestration of carbon in silicates and the structure of magnesite II

Wendy R. Panero

School of Earth Sciences, Division of Earth and Planetary Dynamics, Ohio State University, Columbus, Ohio, USA

Jason E. Kabbes

School of Earth Sciences, Division of Earth and Planetary Dynamics, Ohio State University, Columbus, Ohio, USA

The participation of the deep mantle in the global carbon cycle and its ability to sequester carbon over billion-year time scales depends upon the mineralogical host for carbon. Density-functional theory calculations for MgCO3-magnesite and structures with tetrahedrally coordinated carbon reveal the stability of magnesite up to ∼80 GPa, with a bulk modulus of 110 (±2) GPa. Magnesite undergoes a structural transition to a pyroxene-like structure at ∼80–100 GPa, with a density increase of 4.5–7.1%. Combined with thermodynamic models for the MgSiO3—MgCO3 system, the inter-solubility of MgCO3 with MgSiO3 orthoenstatite and perovskite constrains the carbon content in the silicates to an upper bound of 4 and 20 ppm (wt), respectively. The carbon content in lower mantle silicates is estimated to be no more than 1% of the mantle's total carbon budget for degassed regions, such that in even the mantle's most depleted regions, most carbon must be stored in carbonates or diamond.

Received 23 April 2008; accepted 20 June 2008; published 23 July 2008.

Citation: Panero, W. R., and J. E. Kabbes (2008), Mantle-wide sequestration of carbon in silicates and the structure of magnesite II, Geophys. Res. Lett., 35, L14307, doi:10.1029/2008GL034442.

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