Serpentinite dehydration in the subducted lithosphere produces no B isotopic fractionation
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BORIS DOI
Date of Publication
February 2025
Publication Type
Article
Division/Institute
Author
Ulrich, M. | |
Chatterjee, S. | |
De Hoog, J. |
Subject(s)
Series
Geochemical Perspectives Letters
ISSN or ISBN (if monograph)
2410-3403
Publisher
European Association of Geochemistry
Language
English
Publisher DOI
Description
The fate of boron (B) and its isotopes during serpentinite dehydration is a matter of debate. To contribute to a better understanding of the B isotopic fractionation upon serpentinite dehydration, we present in situ δ11B analyses of antigorite and olivine from subducted high pressure serpentinites from the Western Alps (Zermatt-Saas and Erro-Tobbio). The different isotopic compositions of antigorite in different parts of the units (δ11B of −5 to +10 ‰ and +13 to +19 ‰ for Zermatt-Saas, and δ11B of up to +26 ‰ for Erro-Tobbio) are inherited from variable serpentinisation conditions on the sea floor. Serpentinite dehydration via the brucite-out reaction during subduction produces metamorphic olivine in oxygen (O) isotopic equilibrium with antigorite. This olivine shows near zero B isotopic fractionation with coexisting antigorite (Δ11BOl-Atg of −0.7 ± 3.4 ‰), which implies little B isotopic fractionation during serpentinite dehydration. In contrast, significant B isotopic disequilibrium (Δ11BOl-Atg of +25 ‰) is found between antigorite and olivine formed in shear bands, shear zones and veins, indicating influx of channelled external fluids, including serpentinite-derived fluids from a protolith with a different isotopic composition.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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Ulrich_Boron_GPL2507_SI.pdf | text | Adobe PDF | 30.57 MB | published |