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Serpentinite plays a crucial role in element mobility during seawater hydrothermal alteration of mid-ocean ridge peridotite on the seafloor and fluid metasomatism of peridotite in the subduction zone. However, element mobility and Mg isotope fractionation during serpentinization of peridotites are still uncertain. In order to address this issue, we present a geochemical study of serpentinites and their associated peridotites in the Xigaze ophiolite from southern Tibet. The serpentinites have lower MgO contents and Mg/Si ratios than the peridotites. The low Mg/Si ratios in serpentinites, along with the Isocon calculation results, indicate the Mg loss during serpentinization. In terms of trace elements, the serpentinites have higher contents of Ba, U, Sr and Pb than the peridotites, though both types of ultramafic rocks exhibit similar REE distribution patterns and HFSE contents. The serpentine-magnetite O isotope thermometry yields a relatively low serpentinization temperatures of 200–300 °C. The trace element composition of the serpentinites is distinct from that of forearc serpentinites but consistent with that of mid-ocean ridge ones. The peridotites show mantle-like δ26Mg values of –0.27 to –0.23‰ with an average of –0.25 ± 0.03‰ (2SD, n = 6). In contrast, the serpentinites have systematically higher δ26Mg values of –0.21 to –0.09‰ with an average of –0.16 ± 0.09‰ (2SD, n = 8). The Mg isotope composition of serpentinites shows no correlations with either the chemical weathering proxy or the talc modal content, indicating that the Mg isotope fractionation between serpentinite and peridotite is not caused by chemical weathering of the serpentinites. Instead, it probably resulted from the serpentinization of peridotite on the seafloor. Thus, there is the loss of not only element Mg but also isotopically light Mg during the serpentinization of peridotites. The isotopically heavy Mg serpentinites can be carried to oceanic subduction zones, giving rise to higher δ26Mg mantle sources for various basalts. The isotopically light Mg can be released into the seawater, regulating the Mg isotope composition of seawater in geological history. Taking into account the sources and sinks of Mg in subduction zone fluids, the formation of isotopically heavy Mg serpentinites during seafloor serpentinization can be probably an important process in changing the Mg isotope composition of mantle sources. [ABSTRACT FROM AUTHOR]

The initial Hf isotope composition of zircon in high-grade metamorphic rocks is an important tracer for protolith origin as well as for the growth and evolution of continental crust. However, less attention has been paid to the behavior of Lu-Hf isotopes in peritectic reactions during partial melting of the continental crust. In this paper, we present a combined study of zircon U-Pb ages, Lu-Hf isotopes and trace elements as well as petrology and whole-rock geochemistry for migmatites close to the eastern Himalayan syntaxis in southeastern Tibet. The results show that peritectic zircons in the migmatites have significantly higher 176Hf/177Hf ratios than their protolith zircons. More interestingly, the 176Lu/177Hf ratios and the contents of high field strength elements (such as Nb, Ta, and Hf) and heavy rare earth elements are significantly elevated in the peritectic zircons compared to the protolith zircons. This suggests that garnets with high Lu/Hf ratios and other minerals (such as titanite, ilmenite, amphibole, and biotite) with moderate Lu/Hf ratios were decomposed during crustal anatexis, contributing to the Hf isotope composition of peritectic zircons. This is confirmed by petrographic observations that garnet and biotite occur as residues or remnants in mesosomes (biotite gneiss) and some leucosomes (felsic veins), but are absent in the melanosomes of the target migmatites. Therefore, the peritectic zircons were produced together with anatectic melts through peritectic reactions and acquired the elevated 176Lu/177Hf ratios compared to the inherited zircons from the protoliths if no peritectic garnet was coevally produced during the crustal anatexis. In this regard, the greatly elevated Hf isotope compositions of peritectic zircons in anatectic granites cannot faithfully reflect the Hf isotope composition of parental rocks. As such, great care must be taken when using Hf isotope ratios to trace the nature of parental rocks with respect to magmatic processes and crustal evolution. • Peritectic zircon have higher Lu/Hf and Hf isotopic ratios than protolith zircons. • Peritectic zircon also have higher HFSE contents than protolith zircons. • Minerals with high Lu/Hf ratios than zircon were decomposed during crustal anatexis. [ABSTRACT FROM AUTHOR]