Saskia Erdmann, Michel Pichavant, Fabrice Gaillard
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引用次数: 0
Abstract
If primitive arc magmas are primarily oxidized or if they acquire their oxidizing character during crustal evolution remains debated. Mineral-melt V partitioning is extremely redox sensitive and has the potential to resolve this debate, but critical low-temperature, hydrous experimental partitioning data are limited. We present new experimental V partitioning data for olivine-melt, spinel-melt, and clinopyroxene-melt based on the ≤ 1200 °C, hydrous basalt phase equilibrium experiments of Pichavant et al. (Geochim Cosmochim Acta 66:2193–2209, 2002) and Pichavant and Macdonald (Contrib Mineral Petrol 154:535–558, 2007). Combined with published experimental data, we use our olivine-melt V partitioning coefficients to show that—contrary to previous conclusions—hydrous melt composition, i.e. melt H2O concentration in addition to the concentration of other melt components, affects V partitioning and thus calculated fO2, systematically overestimating fO2 for olivine-melt equilibrated at high melt H2O concentration. False absolute fO2 values and false oxidation or reduction trends may be inferred. Based on these findings, we have calibrated a set of new olivine-melt oxybarometers applicable to hydrous arc magmas partially crystallized at ~ 1025–1350 °C. In a case study on a high-Mg basalt from St. Vincent, Lesser Antilles, we show that olivine-melt V oxybarometry records oxidizing near-liquidus conditions (~ QFM + 1.8) and possibly limited oxidation (~ 0.3 log units) during intermittent crustal magma storage.
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.