¹Jennifer Hanley, ²Vincent F. Chevrier, ³R. Scott Barrows, ⁴Chase Swaffer, ²Travis S. Altheide
¹Department of Space Studies, Southwest Research Institute, Boulder, Colorado, USA
²Arkansas Center for Space and Planetary Sciences, University of Arkansas, Fayetteville, Arkansas, USA
³Center for Astrophysics and Space Astronomy, University of Colorado, Boulder, Colorado, USA

The presence and distribution of oxychlorine salts (e.g. chlorates and perchlorates) on Mars has implications for the stability of water, most notably that they lower the freezing temperature. To date, elemental chlorine has been measured by all lander missions, with the perchlorate ion identified at both the Phoenix and Curiosity landing sites, but detection by near-infrared (NIR) and mid-infrared (MIR) remote sensing has been limited to deposits of anhydrous chlorides. Given that oxychlorine salts can form numerous hydrated phases, we have measured their NIR and MIR reflectance spectra from 1–25 µm for comparison to data collected from orbiting spectrometers. Anhydrous oxychlorine salts show almost no features in the NIR, except for small bands of residual adsorbed water. However, hydrated oxychlorine salts show numerous features due to water in the NIR, specifically at ~1.4 and ~1.9 µm. Increasing the hydration state increases the depth and width of the water bands. All oxychlorine salts exhibit an additional feature at ~2.2 µm due to a Cl-O combination or overtone feature, though it is less prominent in the hydrated perchlorate salts, likely overwhelmed by the ClO4-H2O feature at 2.14 µm. All oxychlorine salts show features in the MIR, due to the fundamental vibrations of Cl-O longward of ~8 µm. The NIR spectral features of hydrated oxychlorine salts are similar to other hydrated salts, especially hydrated sulfates, thus identification from orbit may be ambiguous; however, by utilizing the NIR and MIR laboratory data presented here for comparison, oxychlorine salts may be detectable by orbiting spectrometers.

Reference
Hanley J, Chevrier VF, Barrows RS, Swaffer C, Altheide TS (2015) Near- and mid-infrared reflectance spectra of hydrated oxychlorine salts with implications for Mars. Journal of Geophysical Research (Planets) (in Press)
Link to Article [DOI: 10.1002/2013JE004575]
Published by arrangement with John Wiley & Sons

¹Mario Fischer-Gödde, ^1,2Christoph Burkhardt, ¹Thomas S. Kruijer, ¹Thorsten Kleine
¹Institut für Planetologie, Westfälische Wilhelms-Universität Münster, Wilhelm-Klemm-Str. 10, 48149 Münster, Germany
²Origins Laboratory, Department of Geophysical Sciences, The University of Chicago, IL 60637, USA

Nucleosynthetic isotope anomalies in bulk chondrites and differentiated meteorites reflect variable proportions of isotopically diverse presolar components in bulk planetary bodies, but the origin of these heterogeneities is not well understood. Here, the Ru isotope composition of a comprehensive suite of iron meteorites and bulk samples of ordinary, enstatite and carbonaceous chondrites, as well as acid leachates and an insoluble residue of the Allende chondrite are examined using newly developed multi-collector inductively coupled plasma mass spectrometry techniques. Except for IAB iron meteorites and enstatite chondrites, all investigated meteorites show well-resolved Ru isotope anomalies. Of these, within-group Ru isotopic variations observed for samples from a given chemical group of iron meteorites reflect secondary neutron capture induced during prolonged cosmic ray-exposure. After correction of these cosmogenic effects using Pt isotopes as a neutron-dose monitor, the remaining Ru isotope anomalies are nucleosynthetic in nature and are consistent with a deficit in s-process Ru in iron meteorite parent bodies. Similarly, Ru isotope anomalies in bulk ordinary and carbonaceous chondrites also reflect a deficiency in s-process Ru. The sequential dissolution of Allende reveals the presence of an HF-soluble s-process carrier, which is either an unidentified presolar phase or a component that incorporated s-process Ru liberated from SiC grains during nebular or parent body processes. We show that varying proportions of the s-process carrier identified in Allende resulted in the correlated Ru isotope anomalies observed for bulk meteorites, and that all meteorites (except possibly IAB irons and enstatite chondrites) are depleted in this s-process component relative to Ru from the Earth’s mantle. Bulk meteorites exhibit correlated Ru and Mo isotope anomalies, reflecting variable deficits of a common s-process component, but some iron meteorites and carbonaceous chondrites appear to deviate from this correlation. This may reflect unaccounted cosmic effects on Mo isotopes in iron meteorites, sample heterogeneities in carbonaceous chondrites or nebular and parent body processes acting differently on presolar Mo and Ru components.
The identification of s-deficits in Ru isotopes in almost all iron meteorites and chondrites investigated so far implies that meteorites do not seem to represent the material delivered to the Earth’s mantle as a late veneer after cessation of core formation. However, additional analyses of a more comprehensive set of chondrites are necessary to firmly arrive at this conclusion.

Reference
Fischer-Gödde M, Burkhardt C, Kruijer TS, Kleine T (2015) Ru isotope heterogeneity in the solar protoplanetary disk. Geochimica et Cosmochimica Act (in Press)
Link to Article [doi:10.1016/j.gca.2015.07.032]
Copyright Elsevier