A model of the 3-μm hydration band with Exponentially Modified Gaussian (EMG) profiles: Application to hydrated chondrites and asteroids

1S.Potin,2S.Manigand,1,3P.Beck,1 C.Wolters,1B.Schmitt
Icarus (in Press) Link to Aricle [https://doi.org/10.1016/j.icarus.2020.113686]
1Université Grenoble Alpes, CNRS, IPAG, 414 rue de la Piscine, 38400 Saint-Martin d’Hères, France
2Niels Bohr Institute & Centre for Star and Planet Formation, University of Copenhagen, Øster Voldgade 5–7, DK-1350 Copenhagen K., Denmark
3Institut Universitaire de France, Paris, France
Copyright Elsevier

We present here a new method to model the shape of the 3-μm absorption band in the reflectance spectra of meteorites and small bodies. The band is decomposed into several OH/H2O components using Exponentially Modified Gaussian (EMG) profiles, as well as possible organic components using Gaussian profiles when present. We compare this model to polynomial and multiple Gaussian profile fits and show that the EMGs model returns the best rendering of the shape of the band, with significantly lower residuals. We also propose as an example an algorithm to estimate the error on the band parameters using a bootstrap method. We then present an application of the model to two spectral analyses of smectites subjected to different H2O vapor pressures, and present the variations of the components with decreasing humidity. This example emphasizes the ability of this model to coherently retrieve weak bands that are hidden within much stronger ones.

Carbon isotopic evolution of aqueous fluids in CM chondrites: Clues from in-situ isotope analyses within calcite grains in Yamato-791198

1Wataru Fujiya,1Yuto Aoki,2Takayuki Ushikubo,1Ko Hashizume,3Akira Yamaguchi
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2020.02.003]
1Faculty of Science, Ibaraki University, 2-1-1 Bunkyo, Mito, 310-8512 Ibaraki, Japan
2Kochi Institute for Core Sample Research, Japan Agency for Marine-Earth Science and Technology, 200 Monobe-otsu, Nankoku, Kochi 783-8502, Japan
3National Institute for Polar Research, Midoricho10-3, Tachikawa, Tokyo 190-8518, Japan
Copyright Elsevier

We report the variability in carbon and oxygen isotopic compositions, chemical compositions, and cathodoluminescence intensities within calcite grains in the Yamato-791198 CM chondrite measured by secondary ion mass spectrometry. To understand the change in carbon isotopic compositions during calcite formation, the carbon isotope-analyses were performed on a series of crystal growth bands of each calcite grain. The crystal growth of calcite grains was inferred from comprehensive analyses of oxygen isotopes, chemical compositions, and cathodoluminescence characteristics.

The observed δ18O variations within individual grains are as large as 13‰. The oxygen-isotope data plot on a single straight line with a slope of 0.61 ± 0.06 (2σ) in an oxygen three-isotope diagram. This slope steeper than that of the terrestrial fractionation line indicates that the oxygen isotopic compositions of aqueous fluids evolved from higher δ18O and Δ17O to lower δ18O and Δ17O compositions due to the oxygen-isotope exchange between water and anhydrous silicates in the parent body. Thus, calcite crystals grew from higher Δ17O to lower Δ17O areas. The crystal growth inferred from oxygen isotopic compositions is corroborated by the morphology and cathodoluminescence characteristics of the calcite grains. The minor element concentrations of the calcite grains did not increase/decrease monotonically during calcite formation.

The δ13C variations within individual grains are no more than 4‰ except for one grain. The intra-grain δ13C variations observed here are much smaller than inter-grain δ13C variations of ∼80‰ previously reported. These observations indicate that the carbon isotopic compositions of dissolved carbon species did not change during calcite formation and that they were locally heterogeneous which reflects variable proportions of carbon reservoirs with different isotopic compositions.