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Open access publications by faculty, postdocs, and graduate students in the Department of Earth Sciences.
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Browsing Open Access Publications by Author "Birner, Suzanne K."
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Item Hydrothermal alteration of seafloor peridotites does not influence oxygen fugacity recorded by spinel oxybarometry(Geological Society of America, 2016-06-01) Birner, Suzanne K.; Warren, Jessica M.; Cottrell, Elizabeth; Davis, Fred A.; Suzanne K. Birner, Jessica M. Warren, Elizabeth Cottrell, and Fred A. Davis; Warren, Jessica M.Olivine, orthopyroxene, and spinel compositions within seafloor peridotites yield important information about the nature of Earth’s mantle. Major element compositions of these minerals can be used to calculate oxygen fugacity, a thermodynamic property critical to understanding phase equilibria in the upper mantle. This study examines how hydrothermal alteration at the seafloor influences peridotite chemistry. The Tonga Trench (South Pacific Ocean) exposes lithospheric forearc peridotites that range from highly altered to completely unaltered and provides an ideal sample suite for investigating the effect of alteration on spinel peridotite major element chemistry and calculated oxygen fugacity. Using the Tonga peridotites, we develop a qualitative alteration scale rooted in traditional point-counting methodology. We show that high degrees of serpentinization do not affect mineral parameters such as forsterite number in olivine, iron site occupancy in orthopyroxene, and Fe3+/SFe ratio in spinel. Additionally, while serpentinization is a redox reaction that leaves behind an oxidized residue, the oxygen fugacity recorded by mantle minerals is unaffected by nearby low-temperature serpentinization. As a result, oxygen fugacity measured by spinel oxybarometry in seafloor peridotites is representative of mantle processes, rather than an artifact of late-stage seafloor alteration.Item Revisiting the electron microprobe method of spinel-olivine-orthopyroxene oxybarometry applied to spinel peridotites(Mineralogical Society of America, 2017-02-09) Davis, Fred A.; Cottrell, Elizabeth; Birner, Suzanne K.; Warren, Jessica M.; Lopez, Oscar G.; Fred A. Davis, Elizabeth Cottrell, Suzanne K. Birner, Jessica M. Warren, and Oscar G. Lopez; Warren, Jessica M.Natural peridotite samples containing olivine, orthopyroxene, and spinel can be used to assess the oxygen fugacity (fO2) of the upper mantle. The calculation requires accurate and precise quantification of spinel Fe3+/∑Fe ratios. Wood and Virgo (1989) presented a correction procedure for electron microprobe (EPMA) measurements of spinel Fe3+/∑Fe ratios that relies on a reported correlation between the difference in Fe3+/∑Fe ratio by Mössbauer spectroscopy and by electron microprobe (ΔFe3+/∑FeMöss-EPMA) and the Cr# [Cr/(Al+Cr)] of spinel. This procedure has not been universally adopted, in part, because of debate as to the necessity and effectiveness of the correction. We have performed a series of replicate EPMA analyses of several spinels, previously characterized by Mössbauer spectroscopy, to test the accuracy and precision of the Wood and Virgo correction. While we do not consistently observe a correlation between Cr# and ΔFe3+/∑FeMöss-EPMA in measurements of the correction standards, we nonetheless find that accuracy of Fe3+/ZFe ratios determined for spinel samples treated as unknowns improves when the correction is applied. Uncorrected measurements have a mean ΔFe3+/∑FeMöss-EPMA = 0.031 and corrected measurements have a mean ΔFe3+/∑FeMöss-EPMA = −0.004. We explain how the reliance of the correction on a global correlation between Cr# and MgO concentration in peridotitic spinels improves the accuracy of Fe3+/ZFe ratios despite the absence of a correlation between ΔFe3+/∑FeMöss-EPMA and Cr# in some analytical sessions. Precision of corrected Fe3+/∑Fe ratios depends on the total concentration of Fe, and varies from ±0.012 to ±0.032 (1σ) in the samples analyzed; precision of uncorrected analyses is poorer by approximately a factor of two. We also present an examination of the uncertainties in the calculation contributed by the other variables used to derive fO2. Because there is a logarithmic relationship between the activity of magnetite and logfO2, the uncertainty in fO2 relative to the QFM buffer contributed by the electron microprobe analysis of spinel is asymmetrical and larger at low ferric Fe concentrations (+0.3/−0.4 log units, 1σ, at Fe3+/∑Fe = 0.10) than at higher ferric Fe concentrations (±0.1 log units, 1σ, at Fe3+/EFe = 0.40). Electron microprobe analysis of olivine and orthopyroxene together contribute another ±0.1 to ±0.2 log units of uncertainty (1σ). Uncertainty in the temperature and pressure of equilibration introduce additional errors on the order of tenths of log units to the calculation of relative fO2. We also document and correct errors that appear in the literature when formulating fO2 that, combined, could yield errors in absolute fO2 of greater than 0.75 log units—even with perfectly accurate Fe3+/∑Fe ratios. Finally, we propose a strategy for calculating the activity of magnetite in spinel that preserves information gained during analysis about the ferric iron content of the spinel. This study demonstrates the superior accuracy and precision of corrected EPMA measurements of spinel Fe3+/∑Fe ratios compared to uncorrected measurements. It also provides an objective method for quantifying uncertainties in the calculation of fO2 from spinel peridotite mineral compositions.