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Calculation of oxygen isotope fractionation in hydroxyl-bearing silicates
Authors:Yong-Fei Zheng
Institution:

aInstitute for Mineralogy, Petrology and Geochemistry, University of Tübingen, Wilhelmstrasse 56, D-72074 Tübingen, Germany

bGeochemical Institute, University of Göttingen, Goldschmidtstrasse 1, D-37077 Göttingen, Germany

Abstract:The modified increment method has been applied to the calculation of oxygen isotope fractionation factors for hydroxyl-bearing silicate minerals. The order of 18O enrichment obtained in common rock-forming minerals is: pyrophyllite > kaolinite > tourmaline greater-or-equal, slanted talc > prehnite greater-or-equal, slanted topaz > illite > phengite > lepidolite greater-or-equal, slanted muscovite greater-or-equal, slanted staurolite > epidote > glaucophane > serpentine greater-or-equal, slanted chlorite > tremolite > hornblende > phlogopite greater-or-equal, slanted biotite > humite > norbergite > ilvaite. Hydroxyl-bearing silicates are enriched in 18O relative to hydroxyl groups but depleted in 18O relative to anhydrous counterparts.

Three sets of self-consistent fractionation factors: between quartz and the hydroxyl-bearing silicate minerals, between calcite and the silicate minerals, and between the silicate minerals and water, have been calculated for a temperature range of 0–1200°C. The fractionation factors calculated for mineral pairs are applicable to isotopic geothermometry in igneous, metamorphic and sedimentary petrology. They can be used as a test of isotopic equilibrium or disequilibrium in natural mineral assemblages over all temperature ranges of geological interest. The difference in oxygen isotope composition between the hydroxyl-bearing mineral and the OH group is quantitatively demonstrated to be temperature dependent and, therefore, can be used as a single-mineral geothermometer.

Keywords:
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