Experimental study of the dehydration of 10-Å phase, with implications for its H2O content and stability in subducted lithosphere
The 10-Å phase (TAP) is a hydrous magnesium silicate that forms from the reaction of talc with H 2 O at high pressures. Its high-pressure, low-temperature stability means that it could be a storage site for H 2 O in subduction zones. We have determined the position of the TAP dehydration reaction, T...
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description | The 10-Å phase (TAP) is a hydrous magnesium silicate that forms from the reaction of talc with H
2
O at high pressures. Its high-pressure, low-temperature stability means that it could be a storage site for H
2
O in subduction zones. We have determined the position of the TAP dehydration reaction, TAP = enstatite + coesite + H
2
O, in phase-equilibrium experiments from 5.0 to 7.1 GPa. Because previous studies had suggested that the composition of TAP is a function of synthesis duration, we used a TAP sample that was synthesised for 392 h. Over the pressure interval of our experiments, the dehydration reaction is isothermal, occurring at a temperature of ~690°C. It is coincident, within experimental uncertainty, with the position of the dehydration reaction of TAP synthesised in short experiments (up to 46 h). Above 7.5 GPa, TAP breaks down to enstatite + stishovite + H
2
O. This reaction has a negative d
P
/d
T
and terminates at an invariant point involving the 3.65-Å phase at ~9.5 GPa, 500°C. The zero volume change implied by the isothermal reaction TAP = enstatite + coesite + H
2
O was used to calculate the interlayer H
2
O content of TAP along the reaction. A best-fit H
2
O content of 1 H
2
O pfu was obtained. This H
2
O content is independent of TAP synthesis conditions, suggesting that variations in previously measured H
2
O contents of TAP occur during quenching and decompression of the samples. The stability of TAP in the Earth is probably limited to cold subduction zones, but in these, it could persist to 300 km depth. |
doi_str_mv | 10.1007/s00410-011-0653-0 |
format | Article |
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2
O at high pressures. Its high-pressure, low-temperature stability means that it could be a storage site for H
2
O in subduction zones. We have determined the position of the TAP dehydration reaction, TAP = enstatite + coesite + H
2
O, in phase-equilibrium experiments from 5.0 to 7.1 GPa. Because previous studies had suggested that the composition of TAP is a function of synthesis duration, we used a TAP sample that was synthesised for 392 h. Over the pressure interval of our experiments, the dehydration reaction is isothermal, occurring at a temperature of ~690°C. It is coincident, within experimental uncertainty, with the position of the dehydration reaction of TAP synthesised in short experiments (up to 46 h). Above 7.5 GPa, TAP breaks down to enstatite + stishovite + H
2
O. This reaction has a negative d
P
/d
T
and terminates at an invariant point involving the 3.65-Å phase at ~9.5 GPa, 500°C. The zero volume change implied by the isothermal reaction TAP = enstatite + coesite + H
2
O was used to calculate the interlayer H
2
O content of TAP along the reaction. A best-fit H
2
O content of 1 H
2
O pfu was obtained. This H
2
O content is independent of TAP synthesis conditions, suggesting that variations in previously measured H
2
O contents of TAP occur during quenching and decompression of the samples. The stability of TAP in the Earth is probably limited to cold subduction zones, but in these, it could persist to 300 km depth.</description><identifier>ISSN: 0010-7999</identifier><identifier>EISSN: 1432-0967</identifier><identifier>DOI: 10.1007/s00410-011-0653-0</identifier><identifier>CODEN: CMPEAP</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Dehydration ; Earth and Environmental Science ; Earth Sciences ; Geology ; Geophysics ; Lithosphere ; Low temperature ; Magnesium silicates ; Mineral Resources ; Mineralogy ; Original Paper ; Petrology ; Pressure</subject><ispartof>Contributions to mineralogy and petrology, 2011-12, Vol.162 (6), p.1279-1289</ispartof><rights>Springer-Verlag 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-bd0ac39f9e447703daa0faecd94e80b2637d6bdb1fa8c470d59df032268e59a13</citedby><cites>FETCH-LOGICAL-c315t-bd0ac39f9e447703daa0faecd94e80b2637d6bdb1fa8c470d59df032268e59a13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00410-011-0653-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00410-011-0653-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Pawley, Alison R.</creatorcontrib><creatorcontrib>Chinnery, Nicholas J.</creatorcontrib><creatorcontrib>Clark, Simon M.</creatorcontrib><creatorcontrib>Walter, Michael J.</creatorcontrib><title>Experimental study of the dehydration of 10-Å phase, with implications for its H2O content and stability in subducted lithosphere</title><title>Contributions to mineralogy and petrology</title><addtitle>Contrib Mineral Petrol</addtitle><description>The 10-Å phase (TAP) is a hydrous magnesium silicate that forms from the reaction of talc with H
2
O at high pressures. Its high-pressure, low-temperature stability means that it could be a storage site for H
2
O in subduction zones. We have determined the position of the TAP dehydration reaction, TAP = enstatite + coesite + H
2
O, in phase-equilibrium experiments from 5.0 to 7.1 GPa. Because previous studies had suggested that the composition of TAP is a function of synthesis duration, we used a TAP sample that was synthesised for 392 h. Over the pressure interval of our experiments, the dehydration reaction is isothermal, occurring at a temperature of ~690°C. It is coincident, within experimental uncertainty, with the position of the dehydration reaction of TAP synthesised in short experiments (up to 46 h). Above 7.5 GPa, TAP breaks down to enstatite + stishovite + H
2
O. This reaction has a negative d
P
/d
T
and terminates at an invariant point involving the 3.65-Å phase at ~9.5 GPa, 500°C. The zero volume change implied by the isothermal reaction TAP = enstatite + coesite + H
2
O was used to calculate the interlayer H
2
O content of TAP along the reaction. A best-fit H
2
O content of 1 H
2
O pfu was obtained. This H
2
O content is independent of TAP synthesis conditions, suggesting that variations in previously measured H
2
O contents of TAP occur during quenching and decompression of the samples. The stability of TAP in the Earth is probably limited to cold subduction zones, but in these, it could persist to 300 km depth.</description><subject>Dehydration</subject><subject>Earth and Environmental Science</subject><subject>Earth Sciences</subject><subject>Geology</subject><subject>Geophysics</subject><subject>Lithosphere</subject><subject>Low temperature</subject><subject>Magnesium silicates</subject><subject>Mineral Resources</subject><subject>Mineralogy</subject><subject>Original Paper</subject><subject>Petrology</subject><subject>Pressure</subject><issn>0010-7999</issn><issn>1432-0967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kM1KxDAUhYMoOI4-gLvg2upN_9IsZRgdYWA2ug5pk9gMnaYmKTpbwSfzxcxYwZWryz33nHPhQ-iSwA0BoLceICeQACEJlEWWwBGakTxLE2AlPUYzgHiljLFTdOb9FuJesWKGPpbvg3Jmp_ogOuzDKPfYahxahaVq99KJYGx_kGL-6xMPrfDqGr-Z0GKzGzrT_Bg81tZhEzxepRvc2D7EQix6GStFbToT9tj02I-1HJugJI5Ka_3QKqfO0YkWnVcXv3OOnu-XT4tVst48PC7u1kmTkSIktQTRZEwzleeUQiaFAC1UI1muKqjTMqOyrGVNtKianIIsmNSQpWlZqYIJks3R1dQ7OPs6Kh_41o6ujy85g7SgjAKLJjKZGme9d0rzIdIRbs8J8ANpPpHmkTQ_kOYQM-mU8dHbvyj3V_x_6BvipoNG</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Pawley, Alison R.</creator><creator>Chinnery, Nicholas J.</creator><creator>Clark, Simon M.</creator><creator>Walter, Michael J.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TN</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H96</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L.G</scope><scope>L6V</scope><scope>M2O</scope><scope>M2P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>R05</scope></search><sort><creationdate>20111201</creationdate><title>Experimental study of the dehydration of 10-Å phase, with implications for its H2O content and stability in subducted lithosphere</title><author>Pawley, Alison R. ; Chinnery, Nicholas J. ; Clark, Simon M. ; Walter, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-bd0ac39f9e447703daa0faecd94e80b2637d6bdb1fa8c470d59df032268e59a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Dehydration</topic><topic>Earth and Environmental Science</topic><topic>Earth Sciences</topic><topic>Geology</topic><topic>Geophysics</topic><topic>Lithosphere</topic><topic>Low temperature</topic><topic>Magnesium silicates</topic><topic>Mineral Resources</topic><topic>Mineralogy</topic><topic>Original Paper</topic><topic>Petrology</topic><topic>Pressure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pawley, Alison R.</creatorcontrib><creatorcontrib>Chinnery, Nicholas J.</creatorcontrib><creatorcontrib>Clark, Simon M.</creatorcontrib><creatorcontrib>Walter, Michael J.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oceanic Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Engineering Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><jtitle>Contributions to mineralogy and petrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pawley, Alison R.</au><au>Chinnery, Nicholas J.</au><au>Clark, Simon M.</au><au>Walter, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental study of the dehydration of 10-Å phase, with implications for its H2O content and stability in subducted lithosphere</atitle><jtitle>Contributions to mineralogy and petrology</jtitle><stitle>Contrib Mineral Petrol</stitle><date>2011-12-01</date><risdate>2011</risdate><volume>162</volume><issue>6</issue><spage>1279</spage><epage>1289</epage><pages>1279-1289</pages><issn>0010-7999</issn><eissn>1432-0967</eissn><coden>CMPEAP</coden><abstract>The 10-Å phase (TAP) is a hydrous magnesium silicate that forms from the reaction of talc with H
2
O at high pressures. Its high-pressure, low-temperature stability means that it could be a storage site for H
2
O in subduction zones. We have determined the position of the TAP dehydration reaction, TAP = enstatite + coesite + H
2
O, in phase-equilibrium experiments from 5.0 to 7.1 GPa. Because previous studies had suggested that the composition of TAP is a function of synthesis duration, we used a TAP sample that was synthesised for 392 h. Over the pressure interval of our experiments, the dehydration reaction is isothermal, occurring at a temperature of ~690°C. It is coincident, within experimental uncertainty, with the position of the dehydration reaction of TAP synthesised in short experiments (up to 46 h). Above 7.5 GPa, TAP breaks down to enstatite + stishovite + H
2
O. This reaction has a negative d
P
/d
T
and terminates at an invariant point involving the 3.65-Å phase at ~9.5 GPa, 500°C. The zero volume change implied by the isothermal reaction TAP = enstatite + coesite + H
2
O was used to calculate the interlayer H
2
O content of TAP along the reaction. A best-fit H
2
O content of 1 H
2
O pfu was obtained. This H
2
O content is independent of TAP synthesis conditions, suggesting that variations in previously measured H
2
O contents of TAP occur during quenching and decompression of the samples. The stability of TAP in the Earth is probably limited to cold subduction zones, but in these, it could persist to 300 km depth.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><doi>10.1007/s00410-011-0653-0</doi><tpages>11</tpages></addata></record> |
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subjects | Dehydration Earth and Environmental Science Earth Sciences Geology Geophysics Lithosphere Low temperature Magnesium silicates Mineral Resources Mineralogy Original Paper Petrology Pressure |
title | Experimental study of the dehydration of 10-Å phase, with implications for its H2O content and stability in subducted lithosphere |
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