<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li L</submitter><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>4273</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11794889</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Sulfur (S), an essential volatile in subduction zone magmatism, exhibits higher solubility in aqueous fluids compared to silicate melts. Despite its importance, the partitioning of S between aqueous fluids and silicate melts under the conditions of subduction zone, critical for magma generation and evolution, remains poorly understood. To address this knowledge gap, we performed piston-cylinder experiments at a temperature of 950 ℃ and pressures of 1 and 2 GPa, investigating the effects of various parameters including oxygen fugacity, melt composition, fluid composition (salinity) and pressure on S partitioning between aqueous fluid and silicate melt (D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup>). Our results indicate that the D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> is always large (> > 1), and S prefers to enter the aqueous fluid at high pressures. However, the D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> decreases with increasing pressure from 1 to 2 GPa. Specifically, under reducing conditions (Ni-NiO buffer), D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> decreased from 147 ± 40 to 20 ± 2, whereas under moderately oxidizing conditions (Re-ReO&lt;sub>2&lt;/sub> buffer), it decreased from 27 ± 1 to 20 ± 2. These results stress the strong affinity of S for aqueous fluids at high pressures. Together with the great capacity for S dissolution in the H&lt;sub>2&lt;/sub>O-rich magma within the deep Earth, fluid-saturated felsic magma efficiently transports substantial amounts of S from deep to shallow regions in subduction zone settings. This process plays a crucial role in the formation of giant porphyry deposits and provides a potential source of excess S released during explosive volcanic eruptions.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Sulfur partitioning between aqueous fluids and felsic melts at high pressures: Implications for sulfur migration in subduction zones.</pubmed_title><pmcid>PMC11794889</pmcid><funding_grant_id>41921003</funding_grant_id><funding_grant_id>42250710679</funding_grant_id><funding_grant_id>42073057</funding_grant_id><funding_grant_id>92062222</funding_grant_id><funding_grant_id>42250202</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Xu T</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Xiong X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sulfur partitioning between aqueous fluids and felsic melts at high pressures: Implications for sulfur migration in subduction zones.</name><description>Sulfur (S), an essential volatile in subduction zone magmatism, exhibits higher solubility in aqueous fluids compared to silicate melts. Despite its importance, the partitioning of S between aqueous fluids and silicate melts under the conditions of subduction zone, critical for magma generation and evolution, remains poorly understood. To address this knowledge gap, we performed piston-cylinder experiments at a temperature of 950 ℃ and pressures of 1 and 2 GPa, investigating the effects of various parameters including oxygen fugacity, melt composition, fluid composition (salinity) and pressure on S partitioning between aqueous fluid and silicate melt (D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup>). Our results indicate that the D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> is always large (> > 1), and S prefers to enter the aqueous fluid at high pressures. However, the D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> decreases with increasing pressure from 1 to 2 GPa. Specifically, under reducing conditions (Ni-NiO buffer), D&lt;sub>S&lt;/sub>&lt;sup>fluid/melt&lt;/sup> decreased from 147 ± 40 to 20 ± 2, whereas under moderately oxidizing conditions (Re-ReO&lt;sub>2&lt;/sub> buffer), it decreased from 27 ± 1 to 20 ± 2. These results stress the strong affinity of S for aqueous fluids at high pressures. Together with the great capacity for S dissolution in the H&lt;sub>2&lt;/sub>O-rich magma within the deep Earth, fluid-saturated felsic magma efficiently transports substantial amounts of S from deep to shallow regions in subduction zone settings. This process plays a crucial role in the formation of giant porphyry deposits and provides a potential source of excess S released during explosive volcanic eruptions.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-04T02:09:46.25Z</modification><creation>2025-04-04T02:09:46.25Z</creation></dates><accession>S-EPMC11794889</accession><cross_references><pubmed>39905166</pubmed><doi>10.1038/s41598-025-88649-2</doi></cross_references></HashMap>