Item talk:Q236915
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{
"USGS Publications Warehouse": { "@context": "https://schema.org", "@type": "Article", "additionalType": "Journal Article", "name": "Sulfur isotope fractionation between fluid and andesitic melt: An experimental study", "identifier": [ { "@type": "PropertyValue", "propertyID": "USGS Publications Warehouse IndexID", "value": "70178523", "url": "https://pubs.usgs.gov/publication/70178523" }, { "@type": "PropertyValue", "propertyID": "USGS Publications Warehouse Internal ID", "value": 70178523 }, { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.1016/j.gca.2014.07.015", "url": "https://doi.org/10.1016/j.gca.2014.07.015" } ], "journal": { "@type": "Periodical", "name": "Geochimica et Cosmochimica Acta", "volumeNumber": "142", "issueNumber": null }, "inLanguage": "en", "isPartOf": [ { "@type": "CreativeWorkSeries", "name": "Geochimica et Cosmochimica Acta" } ], "datePublished": "2014", "dateModified": "2016-11-22", "abstract": "Glasses produced from decompression experiments conducted by Fiege et al. (2014a) were used to investigate the fractionation of sulfur isotopes between fluid and andesitic melt upon magma degassing. Starting materials were synthetic glasses with a composition close to a Krakatau dacitic andesite. The glasses contained 4.55\u20137.95\u00a0wt% H2O, \u223c140 to 2700\u00a0ppm sulfur (S), and 0\u20131000\u00a0ppm chlorine (Cl). The experiments were carried out in internally heated pressure vessels (IHPV) at 1030\u00a0\u00b0C and oxygen fugacities (fO2) ranging from QFM+0.8 log units up to QFM+4.2 log units (QFM: quartz\u2013fayalite\u2013magnetite buffer). The decompression experiments were conducted by releasing pressure (P) continuously from \u223c400\u00a0MPa to final P of 150, 100, 70 and 30\u00a0MPa. The decompression rate (r) ranged from 0.01 to 0.17\u00a0MPa/s. The samples were annealed for 0\u201372\u00a0h (annealing time, tA) at the final P and quenched rapidly from 1030\u00a0\u00b0C to room temperature (T).The decompression led to the formation of a S-bearing aqueous fluid phase due to the relatively large fluid\u2013melt partitioning coefficients of S. Secondary ion mass spectrometry (SIMS) was used to determine the isotopic composition of the glasses before and after decompression. Mass balance calculations were applied to estimate the gas\u2013melt S isotope fractionation factor \u03b1g-m.No detectable effect of r and tA on \u03b1g-m was observed. However, SIMS data revealed a remarkable increase of \u03b1g-m from \u223c0.9985\u00a0\u00b1\u00a00.0007 at >QFM+3 to \u223c1.0042\u00a0\u00b1\u00a00.0042 at \u223cQFM+1. Noteworthy, the isotopic fractionation at reducing conditions was about an order of magnitude larger than predicted by previous works. Based on our experimental results and on previous findings for S speciation in fluid and silicate melt a new model predicting the effect of fO2 on \u03b1g-m (or \u039434Sg\u2013m) in andesitic systems at 1030\u00a0\u00b0C is proposed. Our experimental results as well as our modeling are of high importance for the interpretation of S isotope signatures in natural samples (e.g., melt inclusions or volcanic gases).", "description": "21 p.", "publisher": { "@type": "Organization", "name": "Elsevier" }, "author": [ { "@type": "Person", "name": "Fiege, Adrian", "givenName": "Adrian", "familyName": "Fiege", "affiliation": [ { "@type": "Organization", "name": "Department of Earth and Environmental Sciences, University of Michigan, Ann Arbor" } ] }, { "@type": "Person", "name": "Holtz, Fran\u00e7ois", "givenName": "Fran\u00e7ois", "familyName": "Holtz" }, { "@type": "Person", "name": "Shimizu, Nobumichi", "givenName": "Nobumichi", "familyName": "Shimizu", "affiliation": [ { "@type": "Organization", "name": "Woods Hole Oceanographic Institution," } ] }, { "@type": "Person", "name": "Behrens, Harald", "givenName": "Harald", "familyName": "Behrens" }, { "@type": "Person", "name": "Knipping, Jaayke L.", "givenName": "Jaayke L.", "familyName": "Knipping", "affiliation": [ { "@type": "Organization", "name": "Department of Earth and Environmental Sciences, University of Michigan, Ann Arbor" } ] }, { "@type": "Person", "name": "Mandeville, Charlie cmandeville@usgs.gov", "givenName": "Charlie", "familyName": "Mandeville", "email": "cmandeville@usgs.gov", "identifier": { "@type": "PropertyValue", "propertyID": "ORCID", "value": "0000-0002-8485-3689", "url": "https://orcid.org/0000-0002-8485-3689" }, "affiliation": [ { "@type": "Organization", "name": "Office of the AD Hazards", "url": "https://www.usgs.gov/mission-areas/natural-hazards" } ] } ], "funder": [ { "@type": "Organization", "name": "Volcano Hazards Program", "url": "https://www.usgs.gov/programs/VHP" } ] }, "OpenAlex": { "abstract_inverted_index": { "Glasses": [ 0 ], "produced": [ 1 ], "from": [ 2, 78, 100, 118, 140, 222 ], "decompression": [ 3, 91, 114, 148 ], "experiments": [ 4, 60, 92 ], "conducted": [ 5, 94 ], "by": [ 6, 95, 250 ], "Fiege": [ 7 ], 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], "0\u201372": [ 128 ], "h": [ 129 ], "(annealing": [ 130 ], "time,": [ 131 ], "tA)": [ 132 ], "quenched": [ 138 ], "rapidly": [ 139 ], "room": [ 144 ], "temperature": [ 145 ], "(T).": [ 146 ], "led": [ 149 ], "formation": [ 152 ], "S-bearing": [ 155 ], "aqueous": [ 156 ], "phase": [ 158 ], "due": [ 159 ], "relatively": [ 162 ], "large": [ 163 ], "fluid\u2013melt": [ 164 ], "partitioning": [ 165 ], "coefficients": [ 166 ], "S.": [ 168 ], "Secondary": [ 169 ], "ion": [ 170 ], "mass": [ 171 ], "spectrometry": [ 172 ], "(SIMS)": [ 173 ], "was": [ 174, 211, 241 ], "determine": [ 177 ], "isotopic": [ 179, 236 ], "before": [ 184 ], "after": [ 186 ], "decompression.": [ 187 ], "Mass": [ 188 ], "balance": [ 189 ], "calculations": [ 190 ], "applied": [ 192 ], "estimate": [ 194 ], "gas\u2013melt": [ 196 ], "S": [ 197, 263, 306 ], "isotope": [ 198, 307 ], "factor": [ 200 ], "\u03b1g-m.": [ 201 ], "No": [ 202 ], "detectable": [ 203 ], "effect": [ 204, 275 ], "r": [ 206 ], "tA": [ 208 ], "on": [ 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