{"title":"上升过程中板坯衍生流体的成分演变:含水熔体与不含 Cl 或富含 Cl 的含水流体之间的痕量元素分配所产生的影响","authors":"Hajime Taniuchi, Tatsuhiko Kawamoto, Takayuki Nakatani, Osamu Ishizuka, Toshihiro Suzuki, Akihiko Tomiya","doi":"10.1007/s00410-024-02122-3","DOIUrl":null,"url":null,"abstract":"<div><p>Slab-derived supercritical liquids separate into aqueous fluids and hydrous melts during their migration. Separated aqueous fluids further release melt components that cannot be dissolved during ascent. During these processes, elemental partitioning occurs, which may contribute to the geochemical evolution of subduction-zone fluids. Here, we report new experimental results of partition coefficients between a hydrous dacitic melt and Cl-free or Cl-rich aqueous fluids (D<sup>fluid/melt</sup>) for 26 elements at a temperature of 1100°C and pressures of 0.3 and 0.7 GPa using internally-heated pressure vessels. Our results reveal that high-field strength elements (HFSE), except Th, are hardly partitioned into aqueous fluids, regardless of their salinity and pressure conditions. In contrast, the partitioning of other elements varies depending on the fluid salinity. D<sup>fluid/melt</sup> of large-ion lithophile elements (LILE) and U increases with salinity, whereas that of rare earth elements (REE) and Th decreases. These results predict that slab-derived aqueous fluids can evolve to become richer in LILE and U and poorer in HFSE and REE by separating melt components, which explains the LILE- and U-rich and HFSE- and REE-poor characteristics of subduction-zone magmas. This also explains the higher LILE/HFSE and LILE/REE ratios in frontal-arc basalts than in rear-arc basalts: frontal-arc basalts can be generated by the addition of aqueous fluids that sufficiently separate the melt components at shallower depths, whereas rear-arc basalts are generated by the addition of supercritical liquids or aqueous fluid that insufficiently separate the melt components at greater depths. Such separation of melt components from ascending slab-derived fluid can determine the geochemical signature and across-arc compositional variation of subduction-zone magmas.</p></div>","PeriodicalId":526,"journal":{"name":"Contributions to Mineralogy and Petrology","volume":"179 5","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Compositional evolution of slab-derived fluids during ascent: implications from trace-element partition between hydrous melts and Cl-free or Cl-rich aqueous fluids\",\"authors\":\"Hajime Taniuchi, Tatsuhiko Kawamoto, Takayuki Nakatani, Osamu Ishizuka, Toshihiro Suzuki, Akihiko Tomiya\",\"doi\":\"10.1007/s00410-024-02122-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Slab-derived supercritical liquids separate into aqueous fluids and hydrous melts during their migration. Separated aqueous fluids further release melt components that cannot be dissolved during ascent. During these processes, elemental partitioning occurs, which may contribute to the geochemical evolution of subduction-zone fluids. Here, we report new experimental results of partition coefficients between a hydrous dacitic melt and Cl-free or Cl-rich aqueous fluids (D<sup>fluid/melt</sup>) for 26 elements at a temperature of 1100°C and pressures of 0.3 and 0.7 GPa using internally-heated pressure vessels. Our results reveal that high-field strength elements (HFSE), except Th, are hardly partitioned into aqueous fluids, regardless of their salinity and pressure conditions. In contrast, the partitioning of other elements varies depending on the fluid salinity. D<sup>fluid/melt</sup> of large-ion lithophile elements (LILE) and U increases with salinity, whereas that of rare earth elements (REE) and Th decreases. These results predict that slab-derived aqueous fluids can evolve to become richer in LILE and U and poorer in HFSE and REE by separating melt components, which explains the LILE- and U-rich and HFSE- and REE-poor characteristics of subduction-zone magmas. This also explains the higher LILE/HFSE and LILE/REE ratios in frontal-arc basalts than in rear-arc basalts: frontal-arc basalts can be generated by the addition of aqueous fluids that sufficiently separate the melt components at shallower depths, whereas rear-arc basalts are generated by the addition of supercritical liquids or aqueous fluid that insufficiently separate the melt components at greater depths. Such separation of melt components from ascending slab-derived fluid can determine the geochemical signature and across-arc compositional variation of subduction-zone magmas.</p></div>\",\"PeriodicalId\":526,\"journal\":{\"name\":\"Contributions to Mineralogy and Petrology\",\"volume\":\"179 5\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Contributions to Mineralogy and Petrology\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00410-024-02122-3\",\"RegionNum\":2,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Contributions to Mineralogy and Petrology","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s00410-024-02122-3","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
Compositional evolution of slab-derived fluids during ascent: implications from trace-element partition between hydrous melts and Cl-free or Cl-rich aqueous fluids
Slab-derived supercritical liquids separate into aqueous fluids and hydrous melts during their migration. Separated aqueous fluids further release melt components that cannot be dissolved during ascent. During these processes, elemental partitioning occurs, which may contribute to the geochemical evolution of subduction-zone fluids. Here, we report new experimental results of partition coefficients between a hydrous dacitic melt and Cl-free or Cl-rich aqueous fluids (Dfluid/melt) for 26 elements at a temperature of 1100°C and pressures of 0.3 and 0.7 GPa using internally-heated pressure vessels. Our results reveal that high-field strength elements (HFSE), except Th, are hardly partitioned into aqueous fluids, regardless of their salinity and pressure conditions. In contrast, the partitioning of other elements varies depending on the fluid salinity. Dfluid/melt of large-ion lithophile elements (LILE) and U increases with salinity, whereas that of rare earth elements (REE) and Th decreases. These results predict that slab-derived aqueous fluids can evolve to become richer in LILE and U and poorer in HFSE and REE by separating melt components, which explains the LILE- and U-rich and HFSE- and REE-poor characteristics of subduction-zone magmas. This also explains the higher LILE/HFSE and LILE/REE ratios in frontal-arc basalts than in rear-arc basalts: frontal-arc basalts can be generated by the addition of aqueous fluids that sufficiently separate the melt components at shallower depths, whereas rear-arc basalts are generated by the addition of supercritical liquids or aqueous fluid that insufficiently separate the melt components at greater depths. Such separation of melt components from ascending slab-derived fluid can determine the geochemical signature and across-arc compositional variation of subduction-zone magmas.
期刊介绍:
Contributions to Mineralogy and Petrology is an international journal that accepts high quality research papers in the fields of igneous and metamorphic petrology, geochemistry and mineralogy.
Topics of interest include: major element, trace element and isotope geochemistry, geochronology, experimental petrology, igneous and metamorphic petrology, mineralogy, major and trace element mineral chemistry and thermodynamic modeling of petrologic and geochemical processes.