E. Hostettler , J.D. Barnes , J.C. Lassiter , B. Dragovic , A. Satkoski
{"title":"Origins of rodingite-forming fluids from the seafloor to exhumed terranes: Insights from calcium, strontium, and oxygen isotopes","authors":"E. Hostettler , J.D. Barnes , J.C. Lassiter , B. Dragovic , A. Satkoski","doi":"10.1016/j.chemgeo.2025.122775","DOIUrl":null,"url":null,"abstract":"<div><div>Rodingites are metasomatic Ca-rich, Si-poor rocks typically formed on the seafloor during interaction of a gabbroic dike with seawater. However, rodingites are also common in exhumed metamorphic terranes, in which their formation and tectonic history are more complex. Here we measure the O, Ca, and Sr isotope compositions of seafloor and Alpine rodingites from various tectonic settings (obducted oceanic lithosphere, subducted oceanic lithosphere, fossil rifted margins). We focus on andradite-grossular garnet, one of the first phases to crystallize during rodingitization, and clinopyroxene to discern the origins of rodingite-forming fluids and thus the tectonic setting of rodingitization. δ<sup>44/40</sup>Ca values of plagioclase (pl), clinopyroxene (cpx), and calculated whole rock (WR) from altered gabbro (i.e., rodingite protoliths) from the Mid-Atlantic Ridge span a range of ∼0.2 ‰ (1.24 to 1.40 ‰ for pl, <em>n</em> = 2; 1.30 ‰ for cpx, <em>n</em> = 1; 1.29 ‰ for WR, n = 1), whereas, garnet (grt), cpx, and WR from the Western and Central Alpine rodingites span ∼2.8 ‰ (0.01 to 2.52 ‰ for grt, <em>n</em> = 9; −0.32 to 1.58 ‰ for cpx, n = 9; −0.22 to 1.92 ‰ for WR, n = 9). <sup>87</sup>Sr/<sup>86</sup>Sr ratios of mineral separates from the seafloor span from 0.702606 to 0.703700 (0.703516 to 0.703700 for pl, <em>n</em> = 2; 0.702606 for cpx, <em>n</em> = 1) and 0.70330 to 0.710559 for Alpines rodingites (0.704756 to 0.710559 for grt, <em>n</em> = 9; 0.70330 to 0.707080 cpx, n = 9). Lastly, δ<sup>18</sup>O values span ∼1.6 ‰ for the seafloor (5.7 to 6.4 ‰ for pl, <em>n</em> = 2; 4.8 ‰ for cpx. n = 2) and ∼ 6.4 ‰ for Alpine rodingites (−0.4 to 4.5 ‰ for grt, <em>n</em> = 9; 1.7 to 6.0 ‰ for cpx, <em>n</em> = 8). Isotope mass balance modeling shows that these data are overall consistent with rodingitization of a gabbroic dike via seawater on the seafloor and subsequent recrystallization with limited isotopic modification during subduction. A few Alpine rodingites with distinctly high or low δ<sup>44/40</sup>Ca values compared to mantle values (e.g., δ<sup>44/40</sup>Ca<sub>WR</sub> = 1.92 ‰ at Erro-Tobbio and δ<sup>44/40</sup>Ca<sub>WR</sub> = −0.22 ‰ at Lago di Cigana) cannot be explained via metasomatism by seawater using the model presented here, requiring either evolution of the fluid source during rodingitization and associated serpentinization and/or Ca isotope disequilibrium.</div></div>","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"683 ","pages":"Article 122775"},"PeriodicalIF":3.6000,"publicationDate":"2025-04-03","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/S0009254125001652","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}
引用次数: 0
Abstract
Rodingites are metasomatic Ca-rich, Si-poor rocks typically formed on the seafloor during interaction of a gabbroic dike with seawater. However, rodingites are also common in exhumed metamorphic terranes, in which their formation and tectonic history are more complex. Here we measure the O, Ca, and Sr isotope compositions of seafloor and Alpine rodingites from various tectonic settings (obducted oceanic lithosphere, subducted oceanic lithosphere, fossil rifted margins). We focus on andradite-grossular garnet, one of the first phases to crystallize during rodingitization, and clinopyroxene to discern the origins of rodingite-forming fluids and thus the tectonic setting of rodingitization. δ44/40Ca values of plagioclase (pl), clinopyroxene (cpx), and calculated whole rock (WR) from altered gabbro (i.e., rodingite protoliths) from the Mid-Atlantic Ridge span a range of ∼0.2 ‰ (1.24 to 1.40 ‰ for pl, n = 2; 1.30 ‰ for cpx, n = 1; 1.29 ‰ for WR, n = 1), whereas, garnet (grt), cpx, and WR from the Western and Central Alpine rodingites span ∼2.8 ‰ (0.01 to 2.52 ‰ for grt, n = 9; −0.32 to 1.58 ‰ for cpx, n = 9; −0.22 to 1.92 ‰ for WR, n = 9). 87Sr/86Sr ratios of mineral separates from the seafloor span from 0.702606 to 0.703700 (0.703516 to 0.703700 for pl, n = 2; 0.702606 for cpx, n = 1) and 0.70330 to 0.710559 for Alpines rodingites (0.704756 to 0.710559 for grt, n = 9; 0.70330 to 0.707080 cpx, n = 9). Lastly, δ18O values span ∼1.6 ‰ for the seafloor (5.7 to 6.4 ‰ for pl, n = 2; 4.8 ‰ for cpx. n = 2) and ∼ 6.4 ‰ for Alpine rodingites (−0.4 to 4.5 ‰ for grt, n = 9; 1.7 to 6.0 ‰ for cpx, n = 8). Isotope mass balance modeling shows that these data are overall consistent with rodingitization of a gabbroic dike via seawater on the seafloor and subsequent recrystallization with limited isotopic modification during subduction. A few Alpine rodingites with distinctly high or low δ44/40Ca values compared to mantle values (e.g., δ44/40CaWR = 1.92 ‰ at Erro-Tobbio and δ44/40CaWR = −0.22 ‰ at Lago di Cigana) cannot be explained via metasomatism by seawater using the model presented here, requiring either evolution of the fluid source during rodingitization and associated serpentinization and/or Ca isotope disequilibrium.
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.