Elephant Moraine 96029, a very mildly aqueously altered and heated CM carbonaceous chondrite: Implications for the drivers of parent body processing

Elephant Moraine (EET) 96029 is a CMcarbonaceous chondrite regolith breccia with evidence for unusually mild aqueous alteration, a later phase of heating and terrestrial weathering. The presence of phyllosilicates and carbonates within chondrules and the fine-grained matrix indicates that this meteorite was aqueously altered in its parent body. Features showing that water-mediated processing was arrested at a very early stage include a matrix with a low magnesium/iron ratio, chondrules whose mesostasis contains glass and/or quench crystallites, and a gehlenite-bearing calcium- and aluminium-rich inclusion. EET 96029 is also rich in Fe,Ni metal relative to other CM chondrites, and more was present prior to its partial replacement by goethite during Antarctic weathering. In combination, these properties indicate that EET 96029 is one of the least aqueously altered CMs yet described (CM2.7) and so provides new insights into the original composition of its parent body. Following aqueous alteration, and whilst still in the parent body regolith, the meteorite was heated to ~400–600 °C by impacts or solar radiation. Heating led to the amorphisation and dehydroxylation of serpentine, replacement of tochilinite by magnetite, loss of sulphur from the matrix, and modification to the structure of organic matter that includes organic nanoglobules. Significant differences between samples in oxygen isotope compositions, and water/hydroxyl contents, suggests that the meteorite contains lithologies that have undergone different intensities of heating. EET 96029 may be more representative of the true nature of parent body regoliths than many other CM meteorites, and as such can help interpret results from the forthcoming missions to study and return samples from C-complex asteroids

Characterising the CI and CI-like carbonaceous chondrites using thermogravimetric analysis and infrared spectroscopy

The CI and CI-like chondrites provide a record of aqueous alteration in the early solar system. However, the CI-like chondrites differ in having also experienced a late stage period of thermal metamorphism. In order to constrain the nature and extent of the aqueous and thermal alteration, we have investigated the bulk mineralogy and abundance of H2O in the CI and CI-like chondrites using thermogravimetric analysis and infrared spectroscopy. The CI chondrites Ivuna and Orgueil show significant mass loss (28.5–31.8 wt.%) upon heating to 1000 °C due to dehydration and dehydroxylation of abundant phyllosilicates and Fe-(oxy)hydroxides and the decomposition of Fe-sulphides, carbonates and organics. Infrared spectra for Ivuna and Orgueil have a prominent 3-μm feature due to bound −OH/H2O in phyllosilicates and Fe-(oxy)hydroxides and only a minor 11-μm feature from anhydrous silicates. These characteristics are consistent with previous studies indicating that the CI chondrites underwent near-complete aqueous alteration. Similarities in the total abundance of H2O and 3 μm/11 μm ratio suggest that there is no difference in the relative degree of hydration experienced by Ivuna and Orgueil. In contrast, the CI-like chondrites Y-82162 and Y-980115 show lower mass loss (13.8–18.8 wt.%) and contain >50 % less H2O than the CI chondrites. The 3-μm feature is almost absent from spectra of Y-82162 and Y-980115 but the 11-μm feature is intense. The CI-like chondrites experienced thermal metamorphism at temperatures >500 °C that initially caused dehydration and dehydroxylation of phyllosilicates before partial recrystallization back into anhydrous silicates. The surfaces of many C-type asteroids were probably heated through impact metamorphism and/or solar radiation, so thermally altered carbonaceous chondrites are likely good analogues for samples that will be returned by the Hayabusa-2 and OSIRIS-REx missions

Abundances of presolar silicon carbide grains in primitive meteorites determined by NanoSIMS

It has been suggested that the matrices of all chondrites are dominated by a common material with Ivuna-like (CI) abundances of volatiles, presolar grains and insoluble organic matter (IOM) (e.g., Alexander, 2005). However, matrix-normalized abundances of presolar silicon carbide (SiC) grains estimated from their noble gas components show significant variations in even the most primitive chondrites (Huss and Lewis, 1995, Huss et al., 2003), in contradiction to there being a common chondrite matrix material. Here we report presolar SiC abundances determined by NanoSIMS raster ion imaging of IOM extracted from primitive members of different meteorite groups. We show that presolar SiC abundance determinations are comparable between NanoSIMS instruments located at three different institutes, between residues prepared by different demineralization techniques, and between microtomed and non-microtomed samples. Our derived SiC abundances in CR chondrites are comparable to those found in the CI chondrites (∼30 ppm) and are much higher than previously determined by noble gas analyses. The revised higher CR SiC abundances are consistent with the CRs being amongst the most primitive chondrites in terms of the isotopic compositions and disordered nature of their organic matter. Similar abundances between CR1, CR2, and CR3 chondrites indicate aqueous alteration on the CR chondrite parent body has not progressively destroyed SiC grains in them. A low SiC abundance for the reduced CV3 RBT 04133 can be explained by parent body thermal metamorphism at an estimated temperature of ∼440 °C. Minor differences between primitive members of other meteorite classes, which did not experience such high temperatures, may be explained by prolonged oxidation at lower temperatures under which SiC grains formed outer layers of SiO2 that were not thermodynamically stable, leading to progressive degassing/destruction of SiC

Mid-infrared study of the molecular structure variability of insoluble organic matter from primitive chondrites

International audienceInsoluble Organic Matter (IOM) found in primitive meteorites was formed in the Early Solar System and subsequently processed on the parent asteroids. The location, temporal sequence and processes of formation of this IOM are still a matter of debate. In particular, there is no consensus on the actual effect of post-accretional aqueous alteration processes on the chemical composition and structure of IOM. In the most primitive chondrites (types 1 and 2), these alterations have so far been either neglected or generically assigned to oxidation processes induced by fluid circulation. A series of IOM samples extracted from 14 chondrites with extensively documented post-accretional histories have been studied by infrared spectroscopy. Aqueous alteration shows no detectable effect on the chemical composition and structure of IOM within or across chondrite classes. Indeed, the most effective post-accretional process appears to be a high-temperature short-duration heating event and concerns essentially type 2 chondrites. In any case, post-accretional processes cannot account for all the chemical and structural variations of IOM. Chondrites from the CI, CR and CM classes accreted IOM precursors with moderately variable compositions, suggesting a chemical heterogeneity of the protosolar disk. The 3.4 μm band, and possibly its overtones and combinations in the near-infrared range, appear to be tracer(s) of the chemical class and possibly of surface heating processes triggered by impacts

Presolar SiC abundances in primitive meteorites by NanoSIMS raster ion imaging of insoluble organic matter

Here we present results obtained with NanoSIMS raster ion imaging to determine the abundance of presolar SiC in the insoluble organic matter (IOM) extracted from a number of different classes of chondrites (both carbonaceous and ordinary). This builds on previous work [1] aimed at obtaining SiC abundances in primitive meteorites by SIMS and comparing them with noble gas analyses. Both IOM and presolar grains are found in similar CI-like relative abundances in the matrices of the most primitive chondrites [2, 3], indicating that a homogeneous mixture of grains was incorporated in the various parent bodies [3]. Both are then subjected to thermal and hydrothermal processing after parent body formation [4]. However, there are significant variations in the matrix-normalized abundances of SiC grains estimated from noble gases carried by presolar grains, which suggest that the primitive chondrites did not form from a well-mixed reservoir of presolar grains. Variations in the source material were attributed to the destruction of presolar grains by heating in the solar nebula (temperatures that may have exceeded 700°C) and were linked to the volatile element fractionations in chondrites [5]. The CR chondrites have amongst the lowest matrix-normalized SiC abundances, and largest volatile element ractionations, reported in the carbonaceous chondrites [5]. However, they contain the most primitive IOM of any chondrite class [6-7], which has experienced peak temperatures of <300°C [8]. These lowtemperatures could not have affected the SiC grains or their noble gas concentrations, indicating that either the IOM escaped heating (implying that it is not presolar)or SiC was degassed/destroyed at low temperatures, perhaps during parent body processing [3]. Thus, in order to resolve this contradiction, it is necessary to determine SiC abundances independently of noble gases. Ion imaging of SiC grains is a direct technique that has been shown to successfully identify presolar SiC grains amongst others

Micrometeorites soluble organic mixture analysed by Nanospray Ion Source Orbitrap mass spectrometry

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The Multiple Origins of Insoluble Organic Matter from Primitive Chondrites

We present a study by IR and Raman of the insoluble organic matter from 28 CI, CR, CM and ung-C2 chondrites. We evidence a chemical heterogeneity of the solar nebula and that thermal heating was the sole parent body process that modified IOM

Micrometeorites soluble organic mixture analysed by Nanospray Ion Source Orbitrap mass spectrometry

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Laboratory Simulation of Pluto's Atmosphere and Aerosols

International audienceWe will present laboratory investigation of Pluto's atmosphere and its aerosols formation to help understand the data provided by the New Horizons spacecraft

Characterization of laboratory analogs of interstellar/cometary organic residues using very high resolution mass spectrometry

WOS:000324035800012International audienceStudying the chemical composition of organic matter in astrophysical environments is an important means to improve our understanding of its origin and evolution. This organic matter evolves from molecular clouds to protoplanetary disks, and as a final destination, takes part in the formation of many objects of our solar system, such as primitive chondritic material, planetesimals and finally planets. In this contribution, we perform experimental simulations based on the VUV irradiation and warming-up of primitive interstellar ice analogs (CH3OH:NH3:H2O), and characterize, for the first time, the resulting refractory residue, using very high resolution mass spectrometry (VHRMS) with an LTQ-orbitrap-XL instrument. An electrospray source allows ionizing all the molecules having proton donor or acceptor chemical functions, while limiting as much as possible their damages. Thus, this method provides the analysis of the whole ionizable molecules making up the residue. The analysis of the spectra shows that these residues contain a large number of molecules formed of CHNO elements, including macromolecular entities beyond 4000 Da. The average elemental composition of the residue is of H/C = 1.5, N/C = 0.4, O/C = 0.4. These first results are tentatively compared to VHRMS analyses of the soluble organic matter (SOM) present in the Murchison's meteorite, a primitive chondrite of the CM class. The molecular richness observed can be considered as the "first step" of the complex abiotic organic matter in extraterrestrial media. This initial matter, that may be rather universal, could then evolve toward more processed materials in parent bodies, such as comets and asteroids, materials that are then observed and subsequently analyzed in meteorites found on Earth. In addition to providing some insight on the mixture complexity, VHRMS allows for the search of specific molecules. For instance, hexamethylenetetramine (HMT) and some of its derivatives are identified in these residues. With the possibility to characterize the whole residue as well as some specific molecules, we consider that VHRMS is a powerful analytical tool for the understanding of the chemical evolution of organic matter in astrophysical environments. (C) 2013 Elsevier Ltd. All rights reserved