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Subduction of oceanic plates releases large amounts of chlorine and fluorine into the mantle. These halogens are transported into the crust through hydrous melting, where they may be incorporated into minerals such as biotite, apatite, and amphibole. Halogen concentrations are measured in volcanic or plutonic material, while the concentration of Cl and F released from the subducting slab must be calculated based upon the amount of crystallized material and the partition coefficients of each mineral. As amphibole is the most common halogen bearing igneous mineral, it is commonly studied as a bearer of Cl and F. However, the partition coefficient of F between amphibole and a hydrous melt has not been agreed upon by previous studies. Here we show that F is moderately to highly compatible in amphibole, in agreement with other experiments performed at crustal conditions. As amphibole may be able to incorporate a large amount of F, cryptic amphibole crystallization may raise the Cl/F ratio of residual magma, which will then be transported to the surface bearing this geochemical signature, even with little crystallized amphibole present in erupted material. This provides further evidence for the occurrence of cryptic amphibole crystallization, previously predicted based on REE studies and phase equilibria. A better understanding of the halogen reservoirs present in the crust will allow for more accurate estimates of the amount of Cl and F released by subducting slabs. 

A set of 11 clinoamphibole standards with known Fe3+/ΣFe were analyzed for X-ray absorption spectra at the Advanced Photon Source at Argonne National Laboratory. Fe3+/ΣFe of each sample is known from Mössbauer data, and span from 0% to 100% Fe3+/ΣFe. Due to the extreme absorption anisotropy of crystals, we determined the orientation of clinoamphiboles crystals using single-crystal X-ray diffraction and spindle stage techniques. Clinoamphiboles crystal were then analyzed with the beam propagation and polarization axes along known direction relative to the crystallographic basis. Absorption anisotropy was then interpolated to predict the range of absorption magnitudes a clinoamphibole may exhibit at each energy. Partial least square fits for Fe3+/ΣFe indicate predictions are closest to the known Fe3+/ΣFe when comparing the same orientation of each sample in the dataset. Predictions including all orientations, while less accurate, still yield strong results with an R-squared of 0.9 and RMSE of 4.7. The results from this dataset demonstrate the efficacy of XAS as a microanalytical technique for crystalline materials, and functions as a reference dataset to research in oxybarometry. 

Oxygen fugacity is an important but difficult parameter to constrain for primitive arc magmas. In this study, the partitioning behavior of Fe3+/Fe2+ between amphibole and glass synthesized in piston cylinder and cold-seal apparatus experiments is developed as an oxybarometer using x-ray absorption spectroscopy. The amphibole oxybarometer is applicable to hydrous magmas at subduction zone settings, and is here applied to amphibole in mafic enclaves, cumulates, and a basaltic tephra erupted from Shiveluch volcano in Kamchatka with measured Fe3+/FeTotal. The fO2 of primitive melts at the volcano is approximately NNO+2 and is faithfully recorded in amphibole from an amphibole-rich cumulate and the basaltic tephra. Apparently higher fO2 recorded by amphibole in mafic enclaves likely results from partial dehydrogenation of amphibole during residence in a shallow andesite storage region. Using a combination of the new oxybarometer and diffusion modeling, we identify three pulses of mafic magma recharge within two weeks of, a month before, and two to three months before eruption, and find that, at each of these times, the host andesite was recharged by at least two magmas at varying stages of differentiation. Application of the amphibole oxybarometer not only gives insight to magmatic fO2 but also potentially details of shallow magmatic processes. 

Abstract Anisotropic absorption in crystals is routinely observed in many spectroscopic methods and is recognized in visible light optics as pleochroism in crystalline materials. As with other spectrosco-pies, anisotropy in Fe K-edge X-ray absorption spectroscopy (XAS) can serve both as an indicator of the general structural arrangement and as a conundrum in quantifying the proportions of absorbers in crystals. In materials containing multiple absorbers, observed anisotropies can typically be represented by a linear relationship between measured spectroscopic peak intensities and relative absorber concentrations. In this study, oriented XAS analysis of pyroxenes demonstrates that the macroscopic theory that describes visible light absorption anisotropy of triaxially anisotropic materials can also be applied to X-ray absorption in pyroxenes, as long as the orientation and magnitude of the characteristic absorption vectors are known for each energy. Oriented single-crystal XAS analysis of pyroxenes also shows that the measured magnitude of characteristic absorption axes at a given orientation is energy-dependent and cannot be reproduced by linear combination of intermediate spectra. Although the macroscopic model describes a majority of the anisotropy, there is distinct discordance between the observed and interpolated spectra in the pre-edge between 7109 and 7115 eV, which is marked by spikes in RMSE/mean intensity ratio. Absorption indicatrices for samples analyzed in the visible and at X-ray wavelengths are modeled with a three-dimensional (3D) pedal surface, which functions as an empirical way of interpolating between the observed absorption data. This surface only requires a maximum of three coefficients, and results from the summation of 3D lemniscates. An absorption indicatrix model can be used to characterize anisotropic absorption in crystals and provides a way of comparing XAS spectra from randomly oriented crystals, such as those from polished sections, to a database of characterized crystals.