¹Robbin Visser, ¹Timm John, ¹Martina Menneken, ²Markus Patzek, ²Addi Bischoff
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2018.08.037]
¹Freie Universität Berlin, Institut für Geologische Wissenschaften, Malteserstr. 74-100, 12249 Berlin
²Institut für Planetologie, WWU Münster, Wilhelm-Klemm-Str. 10, D-48149 Münster, Germany
Copyright Elsevier

An important question regarding the formation of the solar system is how planetary bodies developed from dust and ice into the planets and planetary bodies. A particularly interesting topic is the thermal evolution of carbonaceous chondrites and volatile-rich clasts that could have originated from CM- and CI-like parent bodies. Two types of these volatile-rich clasts, which are a particular type of dark clasts, can be found. These clasts are mineralogically very similar to CM and CI chondrites and can occasionally be found in achrondritic meteorites. Mineral assemblages suggest that both CM and CI chondrites as well as volatile-rich clasts experienced low peak temperatures. However, these mineral assemblages only offer large estimated temperature ranges to describe the thermal history of CM and CI chondrites, and the thermal history of volatile-rich clasts has not been previously described. In this study, to gain a better understanding of the thermal history of both CM and CI chondrites and volatile-rich clasts, we estimated peak temperatures of 30 volatile-rich clasts (16 CI-, and 14 CM-like) in 10 different host meteorites (4 polymict ureilites, 5 polymict eucrites and 1 howardite) by Raman carbon thermometry. An automated method was developed in order to describe over 4000 collected Raman spectra using four pseudovoigt functions. The full width half maximum (FWHM) of the D1-band was then used to calculate peak temperatures. Results were then compared to Raman data of 8 different well-studied carbonaceous chondrites (including CI and CM chondrites) to evaluate the suggestion that volatile-rich clasts are composed of similar material to the equivalent CI and CM chondrites. Our results show that the peak temperatures experienced by CI-like clasts range between 30-110 °C with an average of about 65 ± 25 °C; the peak temperatures experienced by CM-like clasts range from 50-110 °C with an average of about 70 ± 25 °C. Six of the 8 studied carbonaceous chondrites (CM, CI, CR or C2ungr) also plot in the same low-temperature range between 50 °C and 75 °C and can thus be considered to have formed under similar temperature conditions as the volatile-rich clasts. This is in agreement with previous suggestions, based on their mineral compositions that volatile-rich clasts and CI and CM carbonaceous chondrites are composed of similar materials. The peak temperatures for carbonaceous chondrites determined in this study considerably reduce the range of temperature estimates proposed previously for these chondrites by different methods. By highlighting the ability of our methodology to evaluate data in an automated way, this study shows that Raman carbon thermometry is a good analytical technique for obtaining information about peak temperatures in small and delicate samples.

¹E.Quirico et al. (>10)
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2018.08.029]
¹University Grenoble Alpes, CNRS, Institut de Planétologie et Astrophysique de Grenoble (IPAG), UMR 5274, Grenoble F-38041, France
Copyright Elsevier

Chondrites are exhumed from their parent bodies by impacts, which at the same time can result in heating and mechanical modification (compaction, deformation, fracturing, etc.). However, whether impacts are responsible for the occurrence of heated C2s remains controversial since radiogenic and solar heating have also been invoked to explain them. Here we report a Raman and infrared study of the composition and structure of Insoluble Organic Matter (IOM) in a series of 39 CM and C2-ungrouped chondrites. These parameters are tracers of the extent and nature of thermal metamorphism a meteorite has experienced and reflect the degree to which the thermally driven and irreversible carbonization of IOM has proceeded. We propose a carbon-based classification of heated C2 chondrites that reveals a high occurrence frequency of thermally processed C2 chondrites (> 36 %). This classification is in agreement with the mineralogical classification scheme of [Nakamura (2005) Post-hydration thermal metamorphism of carbonaceous chondrites. J. Mineral. Petrol. Sci. 100, 260–272]. Strongly heated C2 chondrites (PCA 02012, PCA 91008, Y 96720) display an IOM structural evolution that is dissimilar to that of type 3 chondrites that experienced long duration radiogenic thermal metamorphism. These differences almost certainly reflect kinetic constraints on IOM modification during short duration heating events. QUE 93005 is a weakly heated chondrite that experienced a retrograde aqueous alteration. Its very aliphatic-rich IOM points to a parent body hydrogenation through interactions with water. The closed-system conditions required by this mechanism could be satisfied by a kinetic confinement during a very short duration impact. MET 01072, a heavily compacted and uni-axially deformed chondrite, did not experience post-accretional heating. In this case, the deformation features probably reflect a low-velocity impact. In contrast, the weakly metamorphosed chondrite EET 96029 experienced one or several low pressure impacts that triggered mild heating and partial dehydration without deformation features. The study of a series of lithologies from the Tagish Lake C2-ungrouped chondrite confirms the coexistence of various degrees of post-accretional alteration, the most altered lithologies having experienced a moderate degree of heating. Overall, the high prevalence of heating in C2 chondrites, the evidence of short-duration heating in the most heated C2s and the ability of low velocity collisions to trigger heating favor impacts (against solar heating), as the dominant heating mechanism. Finally, our set of data does not support the action of a low temperature oxidation process that would control the aliphatic abundance in unheated primitive C2s.