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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>2018-01-15T18:41:36Z</responseDate> <request identifier=oai:HAL:hal-00644524v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-00644524v1</identifier> <datestamp>2018-01-11</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdu</setSpec> <setSpec>subject:sde</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:INSU</setSpec> <setSpec>collection:SDE</setSpec> <setSpec>collection:GM</setSpec> <setSpec>collection:GIP-BE</setSpec> <setSpec>collection:MNHN</setSpec> <setSpec>collection:AGROPOLIS</setSpec> <setSpec>collection:UNIV-LORRAINE</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:OTELO-UL</setSpec> <setSpec>collection:B3ESTE</setSpec> <setSpec>collection:UNIV-MONTPELLIER</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Volatile-rich Metasomatism in Montferrier Xenoliths (Southern France): Implications for the Abundances of Chalcophile and Highly Siderophile Elements in the Subcontinental Mantle</title> <creator>Alard, Olivier</creator> <creator>Lorand, Jean-Pierre</creator> <creator>Reisberg, Laurie</creator> <creator>Bodinier, Jean-Louis</creator> <creator>Dautria, Jean-Marie</creator> <creator>O'Reilly, Suzanne Y.</creator> <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>Laboratoire de minéralogie du Muséum National d'Histoire Naturelle (LMMNHN) ; Muséum National d'Histoire Naturelle (MNHN) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Centre de Recherches Pétrographiques et Géochimiques (CRPG) ; Université de Lorraine (UL) - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>ARC National Key Centre for Geochemical Evolution and Metallogeny of Continents (GEMOC) ; Macquarie University</contributor> <description>International audience</description> <source>ISSN: 0022-3530</source> <source>EISSN: 1460-2415</source> <source>Journal of Petrology</source> <publisher>Oxford University Press (OUP)</publisher> <identifier>hal-00644524</identifier> <identifier>https://hal.archives-ouvertes.fr/hal-00644524</identifier> <source>https://hal.archives-ouvertes.fr/hal-00644524</source> <source>Journal of Petrology, Oxford University Press (OUP), 2011, 52 (10), pp.2009-2045. 〈10.1093/petrology/egr038〉</source> <identifier>DOI : 10.1093/petrology/egr038</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/petrology/egr038</relation> <language>en</language> <subject lang=en>peridotite</subject> <subject lang=en>sulphide</subject> <subject lang=en>metasomatism</subject> <subject lang=en>mantle</subject> <subject lang=en>highly siderophile elements</subject> <subject lang=en>chalcophile elements</subject> <subject>[SDU.STU.GC] Sciences of the Universe [physics]/Earth Sciences/Geochemistry</subject> <subject>[SDE.MCG] Environmental Sciences/Global Changes</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>Despite a relatively 'uniform' fertile composition (Al2O3 = 2 center dot 19-4 center dot 47 wt %; Fo% = 89 center dot 2 +/- 0 center dot 3%; Cr#(Spl) = 8 center dot 9 +/- 1 center dot 5%), the Montferrier peridotite xenoliths show a wide range of S contents (22-590 ppm). Most sulphides are interstitial and show peculiar pyrrhotite-pentlandite intergrowths and low abundances of Cu-rich phases. Sulphide-rich samples are characterized by strong enrichment in the light rare earth elements and large ion lithophile elements without concomitant enrichment of the high field strength elements. Such trace-element fractionation is commonly ascribed to metasomatism by volatile-rich melts and/or carbonatitic melts. S and Se (11-67 ppb), as well as S/Se (up to approximate to 12 000), are correlated with La/Sm. Cu, however, remains broadly constant (30 +/- 5 ppm). These features strongly suggest that the percolation-reaction of such volatile-rich fluids has led to sulphide enrichment with an atypical signature marked by strong fractionation of the chalcophile elements (i.e. S vs Se and Cu). S-rich xenoliths are also characterized by high (Pd/Ir)(N) (1 center dot 2-1 center dot 9; where subscript N indicates normalized to chondrite), (Pd/Pt)(N) between 1 center dot 5 and 2 center dot 2, and (Os/Ir)(N) up to 1 center dot 85. Despite the relative uniform fertile composition of the xenoliths, Re/Os ranges between 0 center dot 02 and 0 center dot 18. Os-187/Os-188 is extremely variable even within a single sample and can be as high as 0 center dot 1756 for the most S-rich samples. Sulphides show highly fractionated and variable abundances of the highly siderophile elements (HSE) [0 center dot 03 (Pd/Ir)(N) < 1283] and Re-Os isotopic composition (0 center dot 115 < Os-187/Os-188 < 0 center dot 172). Such variation can be observed at the thin-section scale. Whole-rock and in situ sulphide data demonstrate that chalcophile and HSE systematics and the Os isotopic composition of the upper mantle could be significantly modified through metasomatism, even with volatile-rich fluids. These features highlight the complex behaviour of the HSE in fluid-rock percolation-reaction models and suggest a complex interplay between sulphide addition (crystallization or sulphidation) and partial equilibration of pre-existing sulphide. The specific fractionations observed in chemical proxies such as S and Se, Os and Ir, and Pd and Pt, as well as the low abundance of Cu-rich sulphides, suggest that sulphide addition may not have occurred via sulphide melts. Rather, we infer that S was present as a dissolved species in a (supercritical) oxidizing, volatile-rich fluid (C-O-H-S +/- Cl) along with other chalcophile and siderophile elements such as Os, Pd, Re and Au. The highly radiogenic Os composition of this fluid ( Os-187/ Os-188 > 0 center dot 17) would imply that such fluids are derived from an uncommon type of mantle source possibly related to carbonatite melts.</description> <date>2011</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>