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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:31:08Z</responseDate> <request identifier=oai:HAL:hal-01121606v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01121606v1</identifier> <datestamp>2018-01-11</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdu</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:GM</setSpec> <setSpec>collection:AGROPOLIS</setSpec> <setSpec>collection:INSU</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:B3ESTE</setSpec> <setSpec>collection:UNIV-MONTPELLIER</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Fe3+ partitioning systematics between orthopyroxene and garnet in mantle peridotite xenoliths and implications for thermobarometry of oxidized and reduced mantle rocks</title> <creator>Nimis, Paolo</creator> <creator>Goncharov, Alexey</creator> <creator>IONOV, Dmitri</creator> <creator>Mccammon, Catherine</creator> <contributor>Dipartimento di Geoscienze [Padova] ; Universita degli Studi di Padova</contributor> <contributor>Institute of Earth Sciences, Saint Petersburg</contributor> <contributor>Géosciences Montpellier ; Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Manteau et Interfaces ; Géosciences Montpellier ; Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS) - Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Bayerisches Geoinstitut ; Universität Bayreuth</contributor> <description>International audience</description> <source>ISSN: 0010-7999</source> <source>EISSN: 1432-0967</source> <source>Contributions to Mineralogy and Petrology</source> <publisher>Springer Verlag (Germany)</publisher> <publisher>Springer Verlag</publisher> <identifier>hal-01121606</identifier> <identifier>https://hal.archives-ouvertes.fr/hal-01121606</identifier> <source>https://hal.archives-ouvertes.fr/hal-01121606</source> <source>Contributions to Mineralogy and Petrology, Springer Verlag, 2015, 169 (1), pp.6. 〈10.1007/s00410-014-1101-8〉</source> <identifier>DOI : 10.1007/s00410-014-1101-8</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s00410-014-1101-8</relation> <language>en</language> <subject lang=en>Thermobarometry</subject> <subject lang=en>Orthopyroxene</subject> <subject lang=en>Garnet</subject> <subject lang=en>Mantle xenoliths</subject> <subject lang=en>Ferric iron</subject> <subject>[SDU.STU.GC] Sciences of the Universe [physics]/Earth Sciences/Geochemistry</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>We have investigated the partitioning of Fe3+ between orthopyroxene (Opx) and garnet (Grt) in well-equilibrated mantle xenoliths using Mössbauer spectroscopy. The samples cover a wide range of P–T conditions (2.1–6.6 GPa, 690–1,412 °C) and geothermal gradients, and are thus representative for Earth’s upper mantle in both on-craton and off-craton continental settings. Garnet has Fe3+/Fetot ratios of 0.03–0.13 and Fe2O3 contents of 0.24–1.00 wt%. Orthopyroxene has, on average, lower Fe3+/Fetot ratios (0.01–0.09) and Fe2O3 contents (0.05–0.63 wt%). In low-pressure, high-temperature samples, however, Opx is systematically richer in Fe2O3 than the coexisting Grt. The Fe3+ Opx/Grt partition coefficient (DOpx/GrtFe3+) shows no obvious relationship with temperature, but increases with decreasing pressure and with increasing NaOpx. The observed Opx/Grt Fe3+ systematics imply that the Opx–Grt Fe–Mg exchange thermometer is not robust against redox changes if total Fe is treated as Fe2+. An approximate evaluation of errors on T estimates due to redox effects predicts negligible deviations for strongly reduced conditions (<65 °C), but potentially large deviations (> to ≫100 °C) for strongly oxidized conditions, especially at very high pressure and when both P and T are calculated by iteration.</description> <date>2015-01</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>