Yu-Wei She , Jian Sun , Zhi-Yong Zhu , Qiu-Hong Xie , Chen-Xu Pan
{"title":"Origin of rodingites in the Xigaze ophiolite, SW Tibet: Constraints from Ca and Sr isotopes","authors":"Yu-Wei She , Jian Sun , Zhi-Yong Zhu , Qiu-Hong Xie , Chen-Xu Pan","doi":"10.1016/j.chemgeo.2025.123071","DOIUrl":null,"url":null,"abstract":"<div><div>Rodingites, extremely calcium-rich but sodium- and silicon-poor rocks forming through fluid-rock reactions, are crucial for understanding the oceanic cycling of materials. However, the source of calcium in rodingites remains debated. Here, we investigate whole rock Ca and Sr isotopic compositions of samples collected across a continuous section of a rodingite dyke from the Xigaze ophiolite, SW Tibet. The rodingite dyke exhibits progressive metasomatism from core to margin, defining central, transitional, and marginal zones. The dyke displays a wide range of δ<sup>44/40</sup>Ca values from 0.28 ‰ to 1.63 ‰ but limited variation in Sr isotope (<sup>87</sup>Sr/<sup>86</sup>Sr<sub>(<em>i</em>)</sub> = 0.70308–0.70438). The slightly metasomatized central rodingites exhibit lower δ<sup>44/40</sup>Ca values (0.53 ‰ to 0.68 ‰) than MORB, whereas the moderately metasomatized transitional rodingites display significantly lighter Ca isotope compositions (δ<sup>44/40</sup>Ca = 0.28 ‰ to 0.61 ‰). The intensively metasomatized marginal rodingites show the highest δ<sup>44/40</sup>Ca values (0.64 ‰ to 1.63 ‰). The transverse profile of δ<sup>44/40</sup>Ca values across the rodingite dyke reveals clear oscillatory zoning, suggesting multiple fluid sources for Ca during rodingitization. In the early-stage, the mafic dyke was metasomatized by a carbonate-bearing fluid characterized by low δ<sup>44/40</sup>Ca values, which originated from the mixing of deserpentinization-related fluids with marine carbonates during subduction. Subsequently, the dyke experienced more intense metasomatism by a high-δ<sup>44/40</sup>Ca serpentinizing fluid, leading to additional Ca input and an elevation of δ<sup>44/40</sup>Ca values. The gradual increase in <sup>87</sup>Sr/<sup>86</sup>Sr<sub>(<em>i</em>)</sub> ratios from the central zone to the marginal zone indicates that the primary fluids were derived from seawater-triggered serpentinization. This study proposes that during the initial stages of subduction fluids released by serpentinite dehydration dissolved sedimentary carbonates on the subducted oceanic slab. As subduction progressed, extensive dehydration of the surrounding serpentinites produced high-δ<sup>44/40</sup>Ca serpentinizing fluids, which further elevated both δ<sup>44/40</sup>Ca and <sup>87</sup>Sr/<sup>86</sup>Sr<sub>(<em>i</em>)</sub> values of the dyke. The highly variable δ<sup>44/40</sup>Ca values of rodingites from diverse tectonic settings support the model involving multiple fluid contributions with distinct Ca isotopic compositions during rodingitization.</div></div>","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"695 ","pages":"Article 123071"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Geology","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009254125004619","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}
Origin of rodingites in the Xigaze ophiolite, SW Tibet: Constraints from Ca and Sr isotopes
Rodingites, extremely calcium-rich but sodium- and silicon-poor rocks forming through fluid-rock reactions, are crucial for understanding the oceanic cycling of materials. However, the source of calcium in rodingites remains debated. Here, we investigate whole rock Ca and Sr isotopic compositions of samples collected across a continuous section of a rodingite dyke from the Xigaze ophiolite, SW Tibet. The rodingite dyke exhibits progressive metasomatism from core to margin, defining central, transitional, and marginal zones. The dyke displays a wide range of δ44/40Ca values from 0.28 ‰ to 1.63 ‰ but limited variation in Sr isotope (87Sr/86Sr(i) = 0.70308–0.70438). The slightly metasomatized central rodingites exhibit lower δ44/40Ca values (0.53 ‰ to 0.68 ‰) than MORB, whereas the moderately metasomatized transitional rodingites display significantly lighter Ca isotope compositions (δ44/40Ca = 0.28 ‰ to 0.61 ‰). The intensively metasomatized marginal rodingites show the highest δ44/40Ca values (0.64 ‰ to 1.63 ‰). The transverse profile of δ44/40Ca values across the rodingite dyke reveals clear oscillatory zoning, suggesting multiple fluid sources for Ca during rodingitization. In the early-stage, the mafic dyke was metasomatized by a carbonate-bearing fluid characterized by low δ44/40Ca values, which originated from the mixing of deserpentinization-related fluids with marine carbonates during subduction. Subsequently, the dyke experienced more intense metasomatism by a high-δ44/40Ca serpentinizing fluid, leading to additional Ca input and an elevation of δ44/40Ca values. The gradual increase in 87Sr/86Sr(i) ratios from the central zone to the marginal zone indicates that the primary fluids were derived from seawater-triggered serpentinization. This study proposes that during the initial stages of subduction fluids released by serpentinite dehydration dissolved sedimentary carbonates on the subducted oceanic slab. As subduction progressed, extensive dehydration of the surrounding serpentinites produced high-δ44/40Ca serpentinizing fluids, which further elevated both δ44/40Ca and 87Sr/86Sr(i) values of the dyke. The highly variable δ44/40Ca values of rodingites from diverse tectonic settings support the model involving multiple fluid contributions with distinct Ca isotopic compositions during rodingitization.
期刊介绍:
Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry.
The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry.
Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry.
The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.