Journal of Metamorphic Geology · 2003 · 113 citations · 53 references
Natural SciencesEarth SciencesGeologyGeochemistryPetrologySedimentologyMetamorphic FaciesMetamorphic GeochemistryMetamorphic MineralsMetamorphic PetrologyMetamorphic ReactionsMetamorphic RocksMagnesite MineralogyMetamorphic EvolutionMetamorphic Mineral ReactionsMetamorphic MineralogyPetrological AnalysisSubduction Zone DeformationSubduction-zone MetamorphismUhp Metamorphism
Abstract The solid‐state reaction magnesite (MgCO 3 ) + calcite (aragonite) (CaCO 3 ) = dolomite (CaMg(CO 3 ) 2 ) has been identified in metapelites from western Tianshan, China. Petrological studies show that two metamorphic stages are recorded in the metapelites: (1) the peak mineral assemblage of magnesite and calcite pseudomorphs after aragonite which is only preserved as inclusions within dolomite; and (2) the retrograde glaucophane‐chloritoid facies mineral assemblage of glaucophane, chloritoid, dolomite, garnet, paragonite, chlorite and quartz. The peak metamorphic temperatures and pressures are calculated to be 560–600 °C, 4.95–5.07 GPa based on the calcite–dolomite geothermometer and the equilibrium calculation of the reaction dolomite = magnesite + aragonite, respectively. These give direct evidence in UHP metamorphic rocks from Tianshan, China, that carbonate sediments were subducted to greater than 150 km depth. This UHP metamorphism represents a geotherm lower than any previously estimated for subduction metamorphism (< 3.7 °C km −1 ) and is within what was previously considered a ‘forbidden’ condition within Earth. In terms of the carbon cycle, this demonstrates that carbonate sediments can be subducted to at least 150 km depth without releasing significant CO 2 to the overlying mantle wedge.
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Fluid Processes in Subduction Zones
Simon M. Peacock · Science · 1990 · 990 citations
Bernard E. Leake, Alan R. Woolley, C.E.S. Arps et al. · European Journal of Mineralogy · 1997 · 938 citations