Fe-Mg Partitioning between Olivine and High-magnesian Melts and the Nature of Hawaiian Parental Liquids

We conducted 1 atm experiments on a synthetic Hawaiian picrite at f O2 values ranging from the quartz-fayalite-magnetite (QFM) buffer to air and temperatures ranging from 1302 to 1600°C. Along the QFM buffer, olivine is the liquidus phase at ∼1540°C and small amounts of spinel (

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Veröffentlicht in:Journal of petrology 2011-01, Vol.52 (7-8), p.1243-1263
Hauptverfasser: Matzen, Andrew K., Baker, Michael B., Beckett, John R., Stolper, Edward M.
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Baker, Michael B.
Beckett, John R.
Stolper, Edward M.
description We conducted 1 atm experiments on a synthetic Hawaiian picrite at f O2 values ranging from the quartz-fayalite-magnetite (QFM) buffer to air and temperatures ranging from 1302 to 1600°C. Along the QFM buffer, olivine is the liquidus phase at ∼1540°C and small amounts of spinel (
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Along the QFM buffer, olivine is the liquidus phase at ∼1540°C and small amounts of spinel (&lt; 0·2 wt %) are present in experiments conducted at and below 1350°C. The olivine becomes progressively more ferrous with decreasing temperature [Fo92 · 3 to Fo87 · 3, where Fo = 100 × Mg/(Mg + Fe), atomic]; compositions of coexisting liquids reflect the mode and composition of the olivine with concentrations of SiO2, TiO2, Al2O3, and CaO increasing monotonically with decreasing temperature, those of NiO and MgO decreasing, and FeO* (all Fe as FeO) remaining roughly constant. An empirical relationship based on our data, T(°C) = 19·2 × (MgO in liquid, wt %) + 1048, provides a semi-quantitative geothermometer applicable to a range of Hawaiian magma compositions. The olivine-liquid exchange coefficient,  = (FeO/MgO)ol/(FeO/MgO)liq, is 0·345 ± 0·009 (1σ ) for our 11 experiments. A literature database of 446 1 atm experiments conducted within 0·25 log units of the QFM buffer (QFM ± 0·25) yields a median of 0·34; values from single experiments range from 0·41 to 0·13 and are correlated with SiO2 and alkalis in the liquid, as well as the forsterite (Fo) content of the olivine. For 78 experiments with broadly tholeiitic liquid compositions (46-52 wt % SiO2 and  3 wt % Na2O + K2O) coexisting with Fo92 - 80 olivines, and run near QFM (QFM ± 0·25), is approximately independent of composition with a median value of 0·340 ± 0·012 (error is the mean absolute deviation of the 78 olivine-glass pairs from the database that meet these compositional criteria), a value close to the mean value of 0·343 ± 0·008 from our QFM experiments. Thus, over the composition range encompassed by Hawaiian tholeiitic lavas and their parental melts,  ∼ 0·34 and, given the redox conditions and a Fo content for the most magnesian olivine phenocrysts, a parental melt composition can be reconstructed. The calculated compositions of the parental melts are sensitive to the input parameters, decreasing by ∼1 wt % MgO for every log unit increase in the selected f O2 , every 0·5 decrease in the Fo-number of the target olivine, and every 0·015 decrease in . For plausible ranges in redox conditions and Fo-number of the most MgO-rich olivine phenocrysts, the parental liquids for Hawaiian tholeiites are highly magnesian, in the range of 19-21 wt % MgO for Kilauea, Mauna Loa and Mauna Kea.</description><identifier>ISSN: 0022-3530</identifier><identifier>EISSN: 1460-2415</identifier><identifier>DOI: 10.1093/petrology/egq089</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>Journal of petrology, 2011-01, Vol.52 (7-8), p.1243-1263</ispartof><rights>The Author 2011. Published by Oxford University Press. All rights reserved. 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Along the QFM buffer, olivine is the liquidus phase at ∼1540°C and small amounts of spinel (&lt; 0·2 wt %) are present in experiments conducted at and below 1350°C. The olivine becomes progressively more ferrous with decreasing temperature [Fo92 · 3 to Fo87 · 3, where Fo = 100 × Mg/(Mg + Fe), atomic]; compositions of coexisting liquids reflect the mode and composition of the olivine with concentrations of SiO2, TiO2, Al2O3, and CaO increasing monotonically with decreasing temperature, those of NiO and MgO decreasing, and FeO* (all Fe as FeO) remaining roughly constant. An empirical relationship based on our data, T(°C) = 19·2 × (MgO in liquid, wt %) + 1048, provides a semi-quantitative geothermometer applicable to a range of Hawaiian magma compositions. The olivine-liquid exchange coefficient,  = (FeO/MgO)ol/(FeO/MgO)liq, is 0·345 ± 0·009 (1σ ) for our 11 experiments. A literature database of 446 1 atm experiments conducted within 0·25 log units of the QFM buffer (QFM ± 0·25) yields a median of 0·34; values from single experiments range from 0·41 to 0·13 and are correlated with SiO2 and alkalis in the liquid, as well as the forsterite (Fo) content of the olivine. For 78 experiments with broadly tholeiitic liquid compositions (46-52 wt % SiO2 and  3 wt % Na2O + K2O) coexisting with Fo92 - 80 olivines, and run near QFM (QFM ± 0·25), is approximately independent of composition with a median value of 0·340 ± 0·012 (error is the mean absolute deviation of the 78 olivine-glass pairs from the database that meet these compositional criteria), a value close to the mean value of 0·343 ± 0·008 from our QFM experiments. Thus, over the composition range encompassed by Hawaiian tholeiitic lavas and their parental melts,  ∼ 0·34 and, given the redox conditions and a Fo content for the most magnesian olivine phenocrysts, a parental melt composition can be reconstructed. The calculated compositions of the parental melts are sensitive to the input parameters, decreasing by ∼1 wt % MgO for every log unit increase in the selected f O2 , every 0·5 decrease in the Fo-number of the target olivine, and every 0·015 decrease in . For plausible ranges in redox conditions and Fo-number of the most MgO-rich olivine phenocrysts, the parental liquids for Hawaiian tholeiites are highly magnesian, in the range of 19-21 wt % MgO for Kilauea, Mauna Loa and Mauna Kea.</description><issn>0022-3530</issn><issn>1460-2415</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkDFPwzAQhS0EEqWwM3pHoefYSZMRVZQitZQB5uianF2j1GltF9R_T0oRK9PTvXvvDR9jtwLuBZRytKXou7YzhxGZHRTlGRsIlUOSKpGdswFAmiYyk3DJrkL4ABC9DwNmppQsDH9FH220nbPO8BXFLyLHl639tI44uobPrFknGzSOgkXHF9TG8POIa-IvGPeeeKf5DL_QHgP9ILmILZ_b3d424ZpdaGwD3fzqkL1PH98ms2S-fHqePMwTVAJiogqUCLWqdS4JqCSFRY5ZriTo1TjVGQjZX3UtQOtGrbIaMB9rKguAphgrOWRw2q19F4InXW293aA_VAKqI6jqD1R1AtVX7k6Vbr_9P_0NKFJvwg</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Matzen, Andrew K.</creator><creator>Baker, Michael B.</creator><creator>Beckett, John R.</creator><creator>Stolper, Edward M.</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110101</creationdate><title>Fe-Mg Partitioning between Olivine and High-magnesian Melts and the Nature of Hawaiian Parental Liquids</title><author>Matzen, Andrew K. ; Baker, Michael B. ; Beckett, John R. ; Stolper, Edward M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a410t-48a3a0c4cf63e0e9e4a86a56430fb72f5013564cc10ffd4b5c0a67fe9800d8743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matzen, Andrew K.</creatorcontrib><creatorcontrib>Baker, Michael B.</creatorcontrib><creatorcontrib>Beckett, John R.</creatorcontrib><creatorcontrib>Stolper, Edward M.</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of petrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matzen, Andrew K.</au><au>Baker, Michael B.</au><au>Beckett, John R.</au><au>Stolper, Edward M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fe-Mg Partitioning between Olivine and High-magnesian Melts and the Nature of Hawaiian Parental Liquids</atitle><jtitle>Journal of petrology</jtitle><date>2011-01-01</date><risdate>2011</risdate><volume>52</volume><issue>7-8</issue><spage>1243</spage><epage>1263</epage><pages>1243-1263</pages><issn>0022-3530</issn><eissn>1460-2415</eissn><abstract>We conducted 1 atm experiments on a synthetic Hawaiian picrite at f O2 values ranging from the quartz-fayalite-magnetite (QFM) buffer to air and temperatures ranging from 1302 to 1600°C. Along the QFM buffer, olivine is the liquidus phase at ∼1540°C and small amounts of spinel (&lt; 0·2 wt %) are present in experiments conducted at and below 1350°C. The olivine becomes progressively more ferrous with decreasing temperature [Fo92 · 3 to Fo87 · 3, where Fo = 100 × Mg/(Mg + Fe), atomic]; compositions of coexisting liquids reflect the mode and composition of the olivine with concentrations of SiO2, TiO2, Al2O3, and CaO increasing monotonically with decreasing temperature, those of NiO and MgO decreasing, and FeO* (all Fe as FeO) remaining roughly constant. An empirical relationship based on our data, T(°C) = 19·2 × (MgO in liquid, wt %) + 1048, provides a semi-quantitative geothermometer applicable to a range of Hawaiian magma compositions. The olivine-liquid exchange coefficient,  = (FeO/MgO)ol/(FeO/MgO)liq, is 0·345 ± 0·009 (1σ ) for our 11 experiments. A literature database of 446 1 atm experiments conducted within 0·25 log units of the QFM buffer (QFM ± 0·25) yields a median of 0·34; values from single experiments range from 0·41 to 0·13 and are correlated with SiO2 and alkalis in the liquid, as well as the forsterite (Fo) content of the olivine. For 78 experiments with broadly tholeiitic liquid compositions (46-52 wt % SiO2 and  3 wt % Na2O + K2O) coexisting with Fo92 - 80 olivines, and run near QFM (QFM ± 0·25), is approximately independent of composition with a median value of 0·340 ± 0·012 (error is the mean absolute deviation of the 78 olivine-glass pairs from the database that meet these compositional criteria), a value close to the mean value of 0·343 ± 0·008 from our QFM experiments. Thus, over the composition range encompassed by Hawaiian tholeiitic lavas and their parental melts,  ∼ 0·34 and, given the redox conditions and a Fo content for the most magnesian olivine phenocrysts, a parental melt composition can be reconstructed. The calculated compositions of the parental melts are sensitive to the input parameters, decreasing by ∼1 wt % MgO for every log unit increase in the selected f O2 , every 0·5 decrease in the Fo-number of the target olivine, and every 0·015 decrease in . For plausible ranges in redox conditions and Fo-number of the most MgO-rich olivine phenocrysts, the parental liquids for Hawaiian tholeiites are highly magnesian, in the range of 19-21 wt % MgO for Kilauea, Mauna Loa and Mauna Kea.</abstract><pub>Oxford University Press</pub><doi>10.1093/petrology/egq089</doi><tpages>21</tpages><oa>free_for_read</oa></addata></record>
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title Fe-Mg Partitioning between Olivine and High-magnesian Melts and the Nature of Hawaiian Parental Liquids
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