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Pitfalls in geothermobarometry of eclogites: Fe3+ and changes in the mineral chemistry of omphacite at ultrahigh pressures
Authors:Alexander?Proyer  author-information"  >  author-information__contact u-icon-before"  >  mailto:alexander.proyer@uni-graz.at"   title="  alexander.proyer@uni-graz.at"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Edgar?Dachs,Catherine?McCammon
Affiliation:(1) Institut für Mineralogie und Petrologie, Universität Graz, Universitätsplatz 2, 8010 Graz, Austria;(2) Institut für Mineralogie, Universität Salzburg, Hellbrunnerstrasse 34, 5020 Salzburg, Austria;(3) Bayerisches Geoinstitut, Universität Bayreuth, 95440 Bayreuth, Germany
Abstract:The relatively low-variance mineral assemblage of a talc-kyanite eclogite from Dabie Shan enabled application of both conventional geothermobarometers (garnet-clinopyroxene geothermometer and the garnet-omphacite-phengite geobarometer) and a multi-equilibrium method to determine peak P-T conditions (THERMOCALC, ldquoaverage PTrdquo). The results were highly discrepant: 840 °C / 31.1 kbar vs. 590 °C / 29.8 kbar. Mössbauer spectroscopy showed that Fe3+/Fetotal in omphacite was significantly higher than the value obtained from standard formula recalculation. When the activities were corrected for Fe endmembers, geothermobarometry gave consistent results (606 °C / 31.3 kbar vs. 585 °C / 30.8 kbar). These are close to those obtained earlier by ldquoaverage PTrdquo, confirming the robustness of the multi-equilibrium approach. The high Fe3+ concentration in omphacite is best explained using a Ca-eskola endmember Ca0.5[]0.5AlSi2O6and allowing corresponding vacancies in the omphacite structure.Editorial responsibility: W. Schreyer
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