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Solubility and stability of beryl in granitic melts

Beryllium contents of granitic melts at saturation in beryl (± chrysoberyl, phenakite, or quartz) have been determined by forward- and reverse-direction experiments at 650-850°C and 200 MPa using natural beryl or the compositionally equivalent mixture of phenakite + alumina + quartz added to metalum...

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Published in:The American mineralogist 1999-06, Vol.84 (5-6), p.733-745
Main Authors: Evensen, Joseph M, London, David, Wendlandt, Richard F
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description Beryllium contents of granitic melts at saturation in beryl (± chrysoberyl, phenakite, or quartz) have been determined by forward- and reverse-direction experiments at 650-850°C and 200 MPa using natural beryl or the compositionally equivalent mixture of phenakite + alumina + quartz added to metaluminous haplogranite, peraluminous haplogranite, and macusanite (a peraluminous Li, B, F, and P enriched rhyolite obsidian from Macusani, Peru). Chrysoberyl coexists with beryl ± quartz in moderately to strongly peraluminous systems (ASI approximately ≥1.05); the assemblage phenakite + beryl + chrysoberyl is stable in silica-undersaturated bulk composition. The BeO content of the melts, which ranged between 0.03-0.40 wt%, varies principally with temperature (the solubility of beryl falls with decreasing T) and with the activity product of beryl, (αBeO)3(αAl2O3)(αSiO2)6. Beryllia contents are lowest in strongly peraluminous and quartz-saturated haplogranite melts; however, the highest BeO content measured in glass products occurs for the strongly peraluminous macusanite at 850°C (4016 ppm); we infer that the greater solubility of beryl in macusanite melt results from melt speciation reactions involving Li, F, B, and P. For all bulk compositions studied, the BeO content of melt projects to a narrow range of similar values at low T, near the solidus of haplogranite. Thus, metaluminous to peraluminous granitic magmas with and without common volatile and fluxing components will, if cooled to subsolidus temperatures, have similarly low BeO requirements for beryl saturation. The small BeO content of melt near the solidus of haplogranite results in a minor (10°C) depression of the freezing point. Compared to Be-free haplogranite melt, the mean melt composition at the beryl-saturated granite minimum shifts slightly toward quartz. Beryl is common in peraluminous granitic rocks in part because lower BeO contents are required to saturate these melts in beryl, and possibly because these melts acquire higher BeO contents by mica melting reactions at their sources. Beryl is also a common constituent of border-facies assemblages in granitic pegmatite dikes, regardless of their ASI values. This early crystallization of beryl results from the low BeO content required to saturate any granitic melt in beryl at the low T-environments in which pegmatite dikes solidify.
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Chrysoberyl coexists with beryl ± quartz in moderately to strongly peraluminous systems (ASI approximately ≥1.05); the assemblage phenakite + beryl + chrysoberyl is stable in silica-undersaturated bulk composition. The BeO content of the melts, which ranged between 0.03-0.40 wt%, varies principally with temperature (the solubility of beryl falls with decreasing T) and with the activity product of beryl, (αBeO)3(αAl2O3)(αSiO2)6. Beryllia contents are lowest in strongly peraluminous and quartz-saturated haplogranite melts; however, the highest BeO content measured in glass products occurs for the strongly peraluminous macusanite at 850°C (4016 ppm); we infer that the greater solubility of beryl in macusanite melt results from melt speciation reactions involving Li, F, B, and P. For all bulk compositions studied, the BeO content of melt projects to a narrow range of similar values at low T, near the solidus of haplogranite. Thus, metaluminous to peraluminous granitic magmas with and without common volatile and fluxing components will, if cooled to subsolidus temperatures, have similarly low BeO requirements for beryl saturation. The small BeO content of melt near the solidus of haplogranite results in a minor (10°C) depression of the freezing point. Compared to Be-free haplogranite melt, the mean melt composition at the beryl-saturated granite minimum shifts slightly toward quartz. Beryl is common in peraluminous granitic rocks in part because lower BeO contents are required to saturate these melts in beryl, and possibly because these melts acquire higher BeO contents by mica melting reactions at their sources. Beryl is also a common constituent of border-facies assemblages in granitic pegmatite dikes, regardless of their ASI values. 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Chrysoberyl coexists with beryl ± quartz in moderately to strongly peraluminous systems (ASI approximately ≥1.05); the assemblage phenakite + beryl + chrysoberyl is stable in silica-undersaturated bulk composition. The BeO content of the melts, which ranged between 0.03-0.40 wt%, varies principally with temperature (the solubility of beryl falls with decreasing T) and with the activity product of beryl, (αBeO)3(αAl2O3)(αSiO2)6. Beryllia contents are lowest in strongly peraluminous and quartz-saturated haplogranite melts; however, the highest BeO content measured in glass products occurs for the strongly peraluminous macusanite at 850°C (4016 ppm); we infer that the greater solubility of beryl in macusanite melt results from melt speciation reactions involving Li, F, B, and P. For all bulk compositions studied, the BeO content of melt projects to a narrow range of similar values at low T, near the solidus of haplogranite. Thus, metaluminous to peraluminous granitic magmas with and without common volatile and fluxing components will, if cooled to subsolidus temperatures, have similarly low BeO requirements for beryl saturation. The small BeO content of melt near the solidus of haplogranite results in a minor (10°C) depression of the freezing point. Compared to Be-free haplogranite melt, the mean melt composition at the beryl-saturated granite minimum shifts slightly toward quartz. Beryl is common in peraluminous granitic rocks in part because lower BeO contents are required to saturate these melts in beryl, and possibly because these melts acquire higher BeO contents by mica melting reactions at their sources. Beryl is also a common constituent of border-facies assemblages in granitic pegmatite dikes, regardless of their ASI values. This early crystallization of beryl results from the low BeO content required to saturate any granitic melt in beryl at the low T-environments in which pegmatite dikes solidify.</description><subject>alkaline earth metals</subject><subject>beryl</subject><subject>Beryllium</subject><subject>Chemical elements</subject><subject>chrysoberyl</subject><subject>dikes</subject><subject>experimental studies</subject><subject>framework silicates</subject><subject>granites</subject><subject>igneous rocks</subject><subject>intrusions</subject><subject>ion probe</subject><subject>mass spectroscopy</subject><subject>melts</subject><subject>Metals</subject><subject>mineral assemblages</subject><subject>Mineralogy</subject><subject>Minerals</subject><subject>nesosilicates</subject><subject>orthosilicates</subject><subject>oxides</subject><subject>pegmatite</subject><subject>phenakite</subject><subject>phenakite group</subject><subject>plutonic rocks</subject><subject>quartz</subject><subject>ring silicates</subject><subject>silica minerals</subject><subject>silicates</subject><subject>solubility</subject><subject>spectra</subject><subject>spectroscopy</subject><subject>Temperature</subject><issn>0003-004X</issn><issn>1945-3027</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpNkEtLAzEURoMoWKtL94Nbid7cvCZLKVqFggu7cBcymUxJmUdNpkj_vVPahavLhcP54BByz-AJGS-fXUeZMYZKqkBekBkzQlIOqC_JDAA4BRDf1-Qm5y0AIpdmRvjX0O6r2MbxULi-LvLozt_QFFVIh7aIfbFJro9j9EUX2jHfkqvGtTncne-crN9e14t3uvpcfixeVtQJVCOtjZMe0QEooT1HrRstBXrPvffIROCmkk1ZS1BY16hLEIFp5EJhhbrhc_Jw0u7S8LMPebTbYZ_6adEin6QlUzhB9AT5NOScQmN3KXYuHSwDe6xiXWePVay0U5WJfzzxmzBkH0Pvw--Q2vqfe0plQSglDP8DVHxiVA</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Evensen, Joseph M</creator><creator>London, David</creator><creator>Wendlandt, Richard F</creator><general>Mineralogical Society of America</general><general>Walter de Gruyter GmbH</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>F1W</scope><scope>H96</scope><scope>L.G</scope></search><sort><creationdate>19990601</creationdate><title>Solubility and stability of beryl in granitic melts</title><author>Evensen, Joseph M ; London, David ; Wendlandt, Richard F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a426t-d9a5c22a00647c3277f7542cc3ccc214e39b5f8d5062dd27804e1723462b27f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>alkaline earth metals</topic><topic>beryl</topic><topic>Beryllium</topic><topic>Chemical elements</topic><topic>chrysoberyl</topic><topic>dikes</topic><topic>experimental studies</topic><topic>framework silicates</topic><topic>granites</topic><topic>igneous rocks</topic><topic>intrusions</topic><topic>ion probe</topic><topic>mass spectroscopy</topic><topic>melts</topic><topic>Metals</topic><topic>mineral assemblages</topic><topic>Mineralogy</topic><topic>Minerals</topic><topic>nesosilicates</topic><topic>orthosilicates</topic><topic>oxides</topic><topic>pegmatite</topic><topic>phenakite</topic><topic>phenakite group</topic><topic>plutonic rocks</topic><topic>quartz</topic><topic>ring silicates</topic><topic>silica minerals</topic><topic>silicates</topic><topic>solubility</topic><topic>spectra</topic><topic>spectroscopy</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evensen, Joseph M</creatorcontrib><creatorcontrib>London, David</creatorcontrib><creatorcontrib>Wendlandt, Richard F</creatorcontrib><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy &amp; Non-Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><jtitle>The American mineralogist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evensen, Joseph M</au><au>London, David</au><au>Wendlandt, Richard F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solubility and stability of beryl in granitic melts</atitle><jtitle>The American mineralogist</jtitle><date>1999-06-01</date><risdate>1999</risdate><volume>84</volume><issue>5-6</issue><spage>733</spage><epage>745</epage><pages>733-745</pages><issn>0003-004X</issn><eissn>1945-3027</eissn><coden>AMMIAY</coden><abstract>Beryllium contents of granitic melts at saturation in beryl (± chrysoberyl, phenakite, or quartz) have been determined by forward- and reverse-direction experiments at 650-850°C and 200 MPa using natural beryl or the compositionally equivalent mixture of phenakite + alumina + quartz added to metaluminous haplogranite, peraluminous haplogranite, and macusanite (a peraluminous Li, B, F, and P enriched rhyolite obsidian from Macusani, Peru). Chrysoberyl coexists with beryl ± quartz in moderately to strongly peraluminous systems (ASI approximately ≥1.05); the assemblage phenakite + beryl + chrysoberyl is stable in silica-undersaturated bulk composition. The BeO content of the melts, which ranged between 0.03-0.40 wt%, varies principally with temperature (the solubility of beryl falls with decreasing T) and with the activity product of beryl, (αBeO)3(αAl2O3)(αSiO2)6. Beryllia contents are lowest in strongly peraluminous and quartz-saturated haplogranite melts; however, the highest BeO content measured in glass products occurs for the strongly peraluminous macusanite at 850°C (4016 ppm); we infer that the greater solubility of beryl in macusanite melt results from melt speciation reactions involving Li, F, B, and P. For all bulk compositions studied, the BeO content of melt projects to a narrow range of similar values at low T, near the solidus of haplogranite. Thus, metaluminous to peraluminous granitic magmas with and without common volatile and fluxing components will, if cooled to subsolidus temperatures, have similarly low BeO requirements for beryl saturation. The small BeO content of melt near the solidus of haplogranite results in a minor (10°C) depression of the freezing point. Compared to Be-free haplogranite melt, the mean melt composition at the beryl-saturated granite minimum shifts slightly toward quartz. Beryl is common in peraluminous granitic rocks in part because lower BeO contents are required to saturate these melts in beryl, and possibly because these melts acquire higher BeO contents by mica melting reactions at their sources. Beryl is also a common constituent of border-facies assemblages in granitic pegmatite dikes, regardless of their ASI values. This early crystallization of beryl results from the low BeO content required to saturate any granitic melt in beryl at the low T-environments in which pegmatite dikes solidify.</abstract><cop>Washington</cop><pub>Mineralogical Society of America</pub><doi>10.2138/am-1999-5-605</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects alkaline earth metals
beryl
Beryllium
Chemical elements
chrysoberyl
dikes
experimental studies
framework silicates
granites
igneous rocks
intrusions
ion probe
mass spectroscopy
melts
Metals
mineral assemblages
Mineralogy
Minerals
nesosilicates
orthosilicates
oxides
pegmatite
phenakite
phenakite group
plutonic rocks
quartz
ring silicates
silica minerals
silicates
solubility
spectra
spectroscopy
Temperature
title Solubility and stability of beryl in granitic melts
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