¹Timo Hopp,¹Christian Vollmer
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12991]
¹Institut für Planetologie, Westfälische Wilhelms-Universität Münster, Münster, Germany
Published by arrangement with John Wiley & Sons

Nanoscale amorphous silicates are a major component in primitive carbonaceous chondrite matrices and anhydrous interplanetary dust particles. Owing to their metastability and sensitive response to reactions with water, this material is of particular interest in understanding nebular and parent body processes in the early solar system. Here we investigated the amorphous silicate matrix (ASM) in the ungrouped carbonaceous chondrite Acfer 094 regarding its texture, chemical composition, and Fe oxidation state. We applied transmission electron microscopy techniques on six, focused ion beam technique-prepared, electron-transparent lamellae of Acfer 094 to determine the textures of this material. Furthermore, we used energy-dispersive X-ray analysis and electron energy loss spectroscopy to quantify the Fe content and the Fe oxidation state of the ASM. Textural investigations reveal differences in sulfide content, porosity, and distribution of the ASM among the samples, as well as evidence for rare recrystallization of phyllosilicate fibers. The chemical composition reveals mobilization of Fe. Furthermore, the determined Fe3+/ΣFe ratios of the ASM in the six samples display a homogeneously high oxidation state (0.66–0.73). This high and homogeneous Fe oxidation state in the ASM of Acfer 094 disagrees with its formation as a primary phase in a reduced solar gas and must have been induced in a later stage process. Most likely, this process was aqueous alteration on the Acfer 094 parent body, which led to hydration and oxidation of the ASM, which is supported by textural and chemical evidence of aqueous alteration.

^1,2C. Aponte,³Neyda M. Abreu,¹Daniel P. Glavin,¹Jason P. Dworkin,¹Jamie E. Elsila
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12959]
¹Solar System Exploration Division, Code 691, NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
²Department of Chemistry, Catholic University of America, Washington, DC, USA
³Earth Science Program, Pennsylvania State University—Du Bois Campus, Du Bois, Pennsylvania, USA
Published by arrangement with John Wiley & Sons

The analysis of water-soluble organic compounds in meteorites provides valuable insights into the prebiotic synthesis of organic matter and the processes that occurred during the formation of the solar system. We investigated the concentration of aliphatic monoamines present in hot acid water extracts of the unaltered Antarctic carbonaceous chondrites, Dominion Range (DOM) 08006 (CO3) and Miller Range (MIL) 05013 (CO3), and the thermally altered meteorites, Allende (CV3), LAP 02206 (CV3), GRA 06101 (CV3), Allan Hills (ALH) 85002 (CK4), and EET 92002 (CK5). We have also reviewed and assessed the petrologic characteristics of the meteorites studied here to evaluate the effects of asteroidal processing on the abundance and molecular distributions of monoamines. The CO3, CV3, CK4, and CK5 meteorites studied here contain total concentrations of amines ranging from 1.2 to 4.0 nmol g−1 of meteorite; these amounts are 1–3 orders of magnitude below those observed in carbonaceous chondrites from the CI, CM, and CR groups. The low-amine abundances for CV and CK chondrites may be related to their extensive degree of thermal metamorphism and/or to their low original amine content. Although the CO3 meteorites, DOM 08006 and MIL 05013, do not show signs of thermal and aqueous alteration, their monoamine contents are comparable to those observed in moderately/extensively thermally altered CV3, CK4, and CK5 carbonaceous chondrites. The low content of monoamines in pristine CO carbonaceous chondrites suggests that the initial amounts, and not asteroidal processes, play a dominant role in the content of monoamines in carbonaceous chondrites. The primary monoamines, methylamine, ethylamine, and n-propylamine constitute the most abundant amines in the CO3, CV3, CK4, and CK5 meteorites studied here. Contrary to the predominance of n-ω-amino acid isomers in CO3 and thermally altered meteorites, there appears to be no preference for the larger n-amines.