¹Yogita Kadlag, ¹Harry Becker
Chemie der Erde (in Press) Link to Article [http://dx.doi.org/10.1016/j.chemer.2017.01.004]
¹Institut für Geologische Wissenschaften, Freie Universität Berlin, Malteserstrasse 74-100, D-12249 Berlin, Germany
Copyright Elsevier

Osmium isotopic compositions, abundances of highly siderophile elements (HSE: platinum group elements, Re and Au), the chalcogen elements S, Se and Te and major and minor elements were analysed in physically separated size fractions and components of the ordinary chondrites WSG 95300 (H3.3, meteorite find) and Parnallee (LL3.6, meteorite fall). Fine grained magnetic fractions are 268-65 times enriched in HSE compared to the non-magnetic fractions. A significant deviation of some fractions of WSG 95300 from the 4.568 Ga 187Re-187Os isochron was caused by redistribution of Re due to weathering of metal. HSE abundance patterns show that at least four different types of HSE carriers are present in WSG 95300 and Parnallee. The HSE carriers display (i) CI chondritic HSE ratios, (ii) variable Re/Os ratios, (iii) lower than CI chondritic Pd/Ir and Au/Ir and (iv) higher Pt/Ir and Pt/Ru than in CI chondrites. These differences between components clearly indicate the loss of refractory HSE carrier phases before accretion of the components. Tellurium abundances correlate with Pd and are decoupled from S, suggesting that most Te partitioned into metal during the last high-temperature event. Tellurium is depleted in all fractions compared to CI chondrite normalized Se abundances. The depletion of Te is likely associated with the high temperature history of the metal precursors of H and LL chondrites and occurred independent of the metal loss event that depleted LL chondrites in siderophile elements. Most non-magnetic and slightly magnetic fractions have S/Se close to CI chondrites. In contrast, the decoupling of Te and Se from S in magnetic fractions suggests the influence of volatility and metal-silicate partitioning on the abundances of the chalcogen elements. The influence of terrestrial weathering on chalcogen element systematics of these meteorites appears to be negligible.

¹C.M.O’D. Alexander, ²G.D. Cody, ³B.T. De Gregorio, ¹L.R. Nittler, ³R.M. Stroud
Chemie der Erde (in Press) Link to Article [http://dx.doi.org/10.1016/j.chemer.2017.01.007]
¹Dept. Terrestrial Magnetism, Carnegie Institution of Washington, 5241 Broad Branch Road, Washington, DC 20015, USA
²Geophysical Laboratory, Carnegie Institution of Washington, 5251 Broad Branch Road, Washington, DC 20015, USA
³Materials Science and Technology Division, U.S. Naval Research Laboratory, Washington, DC 20375, USA
Copyright Elsevier

All chondrites accreted ∼3.5 wt.% C in their matrices, the bulk of which was in a macromolecular solvent and acid insoluble organic material (IOM). Similar material to IOM is found in interplanetary dust particles (IDPs) and comets. The IOM accounts for almost all of the C and N in chondrites, and a significant fraction of the H. Chondrites and, to a lesser extent, comets were probably the major sources of volatiles for the Earth and the other terrestrial planets. Hence, IOM was both the major source of Earth’s volatiles and a potential source of complex prebiotic molecules.

Large enrichments in D and 15N, relative to the bulk solar isotopic compositions, suggest that IOM or its precursors formed in very cold, radiation-rich environments. Whether these environments were in the interstellar medium (ISM) or the outer Solar System is unresolved. Nevertheless, the elemental and isotopic compositions and functional group chemistry of IOM provide important clues to the origin(s) of organic matter in protoplanetary disks. IOM is modified relatively easily by thermal and aqueous processes, so that it can also be used to constrain the conditions in the solar nebula prior to chondrite accretion and the conditions in the chondrite parent bodies after accretion.

Here we review what is known about the abundances, compositions and physical nature of IOM in the most primitive chondrites. We also discuss how the IOM has been modified by thermal metamorphism and aqueous alteration in the chondrite parent bodies, and how these changes may be used both as petrologic indicators of the intensity of parent body processing and as tools for classification. Finally, we critically assess the various proposed mechanisms for the formation of IOM in the ISM or Solar System.

¹Romy D. Hanna, ¹Richard A. Ketcham
Chemie der Erde (in Press) Link to Article [http://dx.doi.org/10.1016/j.chemer.2017.01.006]
¹Jackson School of Geosciences, University of Texas, 2275 Speedway Stop C9000, Austin, TX 78712, USA
Copyright Elsevier

X-ray computed tomography (XCT) is a powerful 3D imaging technique that has been used to investigate meteorites, mission-returned samples, and other planetary materials of all scales from dust particles to large rocks. With this technique, a 3D volume representing the X-ray attenuation (which is sensitive to composition and density) of the materials within an object is produced, allowing various components and textures to be observed and quantified. As with any analytical technique, a thorough understanding of the underlying physical principles, system components, and data acquisition parameters provides a strong foundation for the optimal acquisition and interpretation of the data. Here we present a technical overview of the physics of XCT, describe the major components of a typical laboratory-based XCT instrument, and provide a guide for how to optimize data collection for planetary materials using such systems. We also discuss data processing, visualization and analysis, including a discussion of common data artifacts and how to minimize them. We review a variety of recent studies in which XCT has been used to study extraterrestrial materials and/or to address fundamental problems in planetary science. We conclude with a short discussion of anticipated future directions of XCT technology and application.