Controls on the solubility of rhenium in silicate melt: Implications for the osmium isotopic composition of Earth's mantle

The solubility of Re and Au in haplobasaltic melt has been investigated at 1673–2573K, 0.1MPa–2GPa and IW−1 to +2.5, in both carbon-saturated and carbon-free systems. Results extend the existing, low pressure and temperature, dataset to more accurately predict the results of metal-silicate equilibri...

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Veröffentlicht in:Earth and planetary science letters 2013-01, Vol.361, p.320-332
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description The solubility of Re and Au in haplobasaltic melt has been investigated at 1673–2573K, 0.1MPa–2GPa and IW−1 to +2.5, in both carbon-saturated and carbon-free systems. Results extend the existing, low pressure and temperature, dataset to more accurately predict the results of metal-silicate equilibrium at the base of a terrestrial magma ocean. Solubilities in run-product glasses were measured by laser ablation ICP-MS, which allows for the explicit assessment of contamination by metal inclusions. The Re and Au content of demonstrably contaminant-free glasses increases with temperature, and shows variation with oxygen fugacity (fO2) similar to previous results, although lower valence states for Re (1+, 2+) are suggested by the data. At 2GPa, and ΔIW of +1.75 to +2, the metal-silicate partition coefficient for Re (DMet/Sil) is defined by the relation LogDMet/SilRe=0.50(±0.022)×104/T(K)+3.73(±0.095) For metal-silicate equilibrium to endow Earth's mantle with the observed time-integrated chondritic Re/Os, (and hence 187Os/188Os), DMet/Sil for both elements must converge to a common value. Combined with previously measured DMet/Sil for Os, the estimated temperature at which this convergence occurs is 4500 (±900)K. At this temperature, however, the Re and Os content of the equilibrated silicate is ∼100-fold too low to explain mantle abundances. In the same experiments, much lower Dmet/sil values have been determined for Au, and require the metal-silicate equilibration temperature to be
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Results extend the existing, low pressure and temperature, dataset to more accurately predict the results of metal-silicate equilibrium at the base of a terrestrial magma ocean. Solubilities in run-product glasses were measured by laser ablation ICP-MS, which allows for the explicit assessment of contamination by metal inclusions. The Re and Au content of demonstrably contaminant-free glasses increases with temperature, and shows variation with oxygen fugacity (fO2) similar to previous results, although lower valence states for Re (1+, 2+) are suggested by the data. At 2GPa, and ΔIW of +1.75 to +2, the metal-silicate partition coefficient for Re (DMet/Sil) is defined by the relation LogDMet/SilRe=0.50(±0.022)×104/T(K)+3.73(±0.095) For metal-silicate equilibrium to endow Earth's mantle with the observed time-integrated chondritic Re/Os, (and hence 187Os/188Os), DMet/Sil for both elements must converge to a common value. Combined with previously measured DMet/Sil for Os, the estimated temperature at which this convergence occurs is 4500 (±900)K. At this temperature, however, the Re and Os content of the equilibrated silicate is ∼100-fold too low to explain mantle abundances. In the same experiments, much lower Dmet/sil values have been determined for Au, and require the metal-silicate equilibration temperature to be &lt;3200K, as hotter conditions result in an excess of Au in the mantle. Thus, the large disparity in partitioning between Re or Os, and Au at core-forming temperatures argues against their mantle concentrations set solely by metal-silicate equilibrium at the base of a terrestrial magma ocean. ► Re solubility in silicate melt increases with temperature and oxygen fugacity. ► An unexpectedly low 2+ valence state for dissolved Re is suggested. ► The solubility of Re is ∼3 orders of magnitude greater than that of Au. ► Re abundances in the mantle cannot be explained by metal-silicate equilibrium. ► The Re/Os ratio of the mantle cannot be set by equilibrium core formation.</description><identifier>ISSN: 0012-821X</identifier><identifier>EISSN: 1385-013X</identifier><identifier>DOI: 10.1016/j.epsl.2012.10.028</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>accretion ; Balancing ; core ; Glass ; Gold ; late veneer ; Mantle ; Melts ; Oceans ; partitioning ; rhenium ; Silicates ; Solubility</subject><ispartof>Earth and planetary science letters, 2013-01, Vol.361, p.320-332</ispartof><rights>2012 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a356t-29024b92941460e74f7ba0e23ea897baf926f7e6453423410b8c9673e30bbdfd3</citedby><cites>FETCH-LOGICAL-a356t-29024b92941460e74f7ba0e23ea897baf926f7e6453423410b8c9673e30bbdfd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0012821X12005973$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Bennett, Neil R.</creatorcontrib><creatorcontrib>Brenan, James M.</creatorcontrib><title>Controls on the solubility of rhenium in silicate melt: Implications for the osmium isotopic composition of Earth's mantle</title><title>Earth and planetary science letters</title><description>The solubility of Re and Au in haplobasaltic melt has been investigated at 1673–2573K, 0.1MPa–2GPa and IW−1 to +2.5, in both carbon-saturated and carbon-free systems. Results extend the existing, low pressure and temperature, dataset to more accurately predict the results of metal-silicate equilibrium at the base of a terrestrial magma ocean. Solubilities in run-product glasses were measured by laser ablation ICP-MS, which allows for the explicit assessment of contamination by metal inclusions. The Re and Au content of demonstrably contaminant-free glasses increases with temperature, and shows variation with oxygen fugacity (fO2) similar to previous results, although lower valence states for Re (1+, 2+) are suggested by the data. At 2GPa, and ΔIW of +1.75 to +2, the metal-silicate partition coefficient for Re (DMet/Sil) is defined by the relation LogDMet/SilRe=0.50(±0.022)×104/T(K)+3.73(±0.095) For metal-silicate equilibrium to endow Earth's mantle with the observed time-integrated chondritic Re/Os, (and hence 187Os/188Os), DMet/Sil for both elements must converge to a common value. Combined with previously measured DMet/Sil for Os, the estimated temperature at which this convergence occurs is 4500 (±900)K. At this temperature, however, the Re and Os content of the equilibrated silicate is ∼100-fold too low to explain mantle abundances. In the same experiments, much lower Dmet/sil values have been determined for Au, and require the metal-silicate equilibration temperature to be &lt;3200K, as hotter conditions result in an excess of Au in the mantle. Thus, the large disparity in partitioning between Re or Os, and Au at core-forming temperatures argues against their mantle concentrations set solely by metal-silicate equilibrium at the base of a terrestrial magma ocean. ► Re solubility in silicate melt increases with temperature and oxygen fugacity. ► An unexpectedly low 2+ valence state for dissolved Re is suggested. ► The solubility of Re is ∼3 orders of magnitude greater than that of Au. ► Re abundances in the mantle cannot be explained by metal-silicate equilibrium. ► The Re/Os ratio of the mantle cannot be set by equilibrium core formation.</description><subject>accretion</subject><subject>Balancing</subject><subject>core</subject><subject>Glass</subject><subject>Gold</subject><subject>late veneer</subject><subject>Mantle</subject><subject>Melts</subject><subject>Oceans</subject><subject>partitioning</subject><subject>rhenium</subject><subject>Silicates</subject><subject>Solubility</subject><issn>0012-821X</issn><issn>1385-013X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EEuXxA6y8g02CH4mbIDao4lGpEhuQ2FmOO1FdOXHwuEjw9SQta1Yzc-fckeYScsVZzhlXt9scBvS5YFyMQs5EdURmXFZlxrj8OCYzNm6ySvCPU3KGuGWMqVLVM_KzCH2KwSMNPU0boBj8rnHepW8aWho30LtdR11PcRStSUA78OmOLrthP7vQI21D3JsDdnsaQwqDs9SGbgjoJmi69mhi2lwj7UyfPFyQk9Z4hMu_ek7enx7fFi_Z6vV5uXhYZUaWKmWiZqJoalEXvFAM5kU7bwwDIcFU9di2tVDtHFRRykLIgrOmsrWaS5CsadbtWp6Tm8PdIYbPHWDSnUML3psewg41l7xUTFWiHlFxQG0MiBFaPUTXmfitOdNT0Hqrp6D1FPSkjUGPpvuDCcYnvhxEjdZBb2HtItik18H9Z_8FPx2I6w</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Bennett, Neil R.</creator><creator>Brenan, James M.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20130101</creationdate><title>Controls on the solubility of rhenium in silicate melt: Implications for the osmium isotopic composition of Earth's mantle</title><author>Bennett, Neil R. ; Brenan, James M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a356t-29024b92941460e74f7ba0e23ea897baf926f7e6453423410b8c9673e30bbdfd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>accretion</topic><topic>Balancing</topic><topic>core</topic><topic>Glass</topic><topic>Gold</topic><topic>late veneer</topic><topic>Mantle</topic><topic>Melts</topic><topic>Oceans</topic><topic>partitioning</topic><topic>rhenium</topic><topic>Silicates</topic><topic>Solubility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bennett, Neil R.</creatorcontrib><creatorcontrib>Brenan, James M.</creatorcontrib><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Earth and planetary science letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bennett, Neil R.</au><au>Brenan, James M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controls on the solubility of rhenium in silicate melt: Implications for the osmium isotopic composition of Earth's mantle</atitle><jtitle>Earth and planetary science letters</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>361</volume><spage>320</spage><epage>332</epage><pages>320-332</pages><issn>0012-821X</issn><eissn>1385-013X</eissn><abstract>The solubility of Re and Au in haplobasaltic melt has been investigated at 1673–2573K, 0.1MPa–2GPa and IW−1 to +2.5, in both carbon-saturated and carbon-free systems. Results extend the existing, low pressure and temperature, dataset to more accurately predict the results of metal-silicate equilibrium at the base of a terrestrial magma ocean. Solubilities in run-product glasses were measured by laser ablation ICP-MS, which allows for the explicit assessment of contamination by metal inclusions. The Re and Au content of demonstrably contaminant-free glasses increases with temperature, and shows variation with oxygen fugacity (fO2) similar to previous results, although lower valence states for Re (1+, 2+) are suggested by the data. At 2GPa, and ΔIW of +1.75 to +2, the metal-silicate partition coefficient for Re (DMet/Sil) is defined by the relation LogDMet/SilRe=0.50(±0.022)×104/T(K)+3.73(±0.095) For metal-silicate equilibrium to endow Earth's mantle with the observed time-integrated chondritic Re/Os, (and hence 187Os/188Os), DMet/Sil for both elements must converge to a common value. Combined with previously measured DMet/Sil for Os, the estimated temperature at which this convergence occurs is 4500 (±900)K. At this temperature, however, the Re and Os content of the equilibrated silicate is ∼100-fold too low to explain mantle abundances. In the same experiments, much lower Dmet/sil values have been determined for Au, and require the metal-silicate equilibration temperature to be &lt;3200K, as hotter conditions result in an excess of Au in the mantle. Thus, the large disparity in partitioning between Re or Os, and Au at core-forming temperatures argues against their mantle concentrations set solely by metal-silicate equilibrium at the base of a terrestrial magma ocean. ► Re solubility in silicate melt increases with temperature and oxygen fugacity. ► An unexpectedly low 2+ valence state for dissolved Re is suggested. ► The solubility of Re is ∼3 orders of magnitude greater than that of Au. ► Re abundances in the mantle cannot be explained by metal-silicate equilibrium. ► The Re/Os ratio of the mantle cannot be set by equilibrium core formation.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.epsl.2012.10.028</doi><tpages>13</tpages></addata></record>
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subjects accretion
Balancing
core
Glass
Gold
late veneer
Mantle
Melts
Oceans
partitioning
rhenium
Silicates
Solubility
title Controls on the solubility of rhenium in silicate melt: Implications for the osmium isotopic composition of Earth's mantle
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