Les chondrites carbonées de type 1 et 2 comprennent les météorites les plus primitives d’un point de vue chimique et pétrologique. Ce caractère primitif est associé à l’abondance de matière organique qui est une phase privilégiée pour l’étude des phénomènes concernant l’héritage du matériel présolaire et sa transformation dans la nébuleuse puis sur les premiers corps. L’objet de cette thèse est l’étude de l’influence des processus post-accrétionnels sur les caractéristiques moléculaires de la matière organique et en particulier la mesure des effets d’oxydation dus à l’altération aqueuse. Nous avons mené une étude comparative basée sur la structure carbonée et l’analyse des fonctions oxygénées et soufrées d’une dizaine de météorites dont les histoires géologiques ont été déterminées par ailleurs. Le degré d’oxydation du soufre, hétéroatome mineur dans la fraction insoluble, a été mesuré par micro-spectrométrie SK-Xanes. La spectroscopie FT-IR a permis la description des structures fines des chaines carbonées et des fonctions riches en oxygène, hétéroatome majeur. La spectrométrie de masse à très haute résolution Orbitrap a été utilisée pour décrire la diversité hétéroatomique des molécules solubles de la chondrite Renazzo (CR2). Les chaines carbonées des chondrites de classe CI et Murchison se différencient de celle des autres météorites par une abondance en groupements terminaux méthyles à la fois supérieure et invariable. Les chondrites de type 1 sont les seules porteuses de fonctions soufrées oxydées acides alors que la spéciation du soufre dans les chondrites de type 2 est invariable. De la même façon, et cette fois pour l’ensemble des chondrites étudiées, les groupements carbonyles sont majoritairement dans les fonctions cétones, en proportion indépendante du degré d’altération aqueuse. Tous les paramètres mesurés dans cette étude nous poussent à conclure que la variabilité moléculaire au sein des chondrites carbonées de type 1 et 2 trouve moins son origine dans l’empreinte de l’hydrothermalisme que dans une hétérogénéité du précurseur organique accrété par chaque corps parent. En particulier, nos mesures invalident l’hypothèse selon laquelle l’altération serait à l’origine d’une conversion oxydative des chaines carbonées en fonctions acides carboxyliques. / Type 1 and 2 carbonaceous chondrites include the most chemically and petrologically pristine meteorites. This intactness goes along with the abundance of organic matter which is a phase of choice to investigate the presolar material processing in the nebula and then on the first bodies. The purpose of this thesis is to study the influence of post-accretional processes on the molecular characteristics of organic matter and in particular the extent of oxidation effects due to aqueous alteration. We have carried out a comparative study based on the carbon structure and functional analysis of more than ten meteorites whose geologic histories were independently determined. The redox degree of sulfur in the insoluble fraction was measured by SK-Xanes spectroscopy. FT-IR spectroscopy gave access to the fine structures of aliphatic chains and oxygen-rich functions. Orbitrap very high resolution mass spectrometry was used to describe the heteroatomic diversity of soluble molecules in the Renazzo (CR2) chondrite. The aliphatic chains of CI chondrites and Murchison differ from others by a higher and unchanging abundance of methyl groups. Type 1 chondrites are the only carriers of oxidized sulfur functions whereas the sulfur speciation in type 2 chondrites is invariable. For all studied chondrites, the carbonyl groups are mainly under the form of ketones and their abundance can’t be related to the degree of aqueous alteration. Any parameters we have measured in this study lead us to conclude that the molecular variability among type 1 and 2 carbonaceous chondrites are less due to the footprint left by the hydrothermal activity than due to the heterogeneity of an organic precursor accreted by each parent body. In particular, our measurements invalidate the hypothesis that the alteration would cause an oxidative conversion of aliphatic chains to carboxylic acid functions.

Les astéroïdes sont des vestiges datant de la formation de notre Système stellaire. Ils nous offrent une opportunité unique de comprendre la mécanique de formation d'un système planétaire habité, le Système Solaire. Une méthode de caractérisation de ces petits corps couramment utilisé est la spectroscopie en réflectance, qui permet à, depuis la Terre ou lors de missions spatiales, d'obtenir des informations sur la minéralogie de ces objets. L'objet de cette thèse est de participer à une meilleure compréhension de cette technique de caractérisation, ainsi que d'étudier, via les météorites, les processus d'altérations ayant modifiés la composition initiale. Pour ce faire nous avons utilisé différentes méthodes d'analyses sur des chondrites carbonées (qui proviennent d'astéroïdes primitifs) afin de caractériser leur chimie et leur minéralogie. Nous avons ainsi étudié les phases hydratées, la teneur en eau, la structure des silicates et l'état d'oxydation du fer de ces météorites. Toutes ces analyses combinées nous ont permis de mieux comprendre l'évolution de la minéralogie en fonction des processus d'altérations hydrothermaux. Ces études ont également permis d'apporter des contraintes quantitatives et qualitatives sur les caractéristiques contrôlant les spectres en réflectance de ces mêmes météorites. Nous avons étudié et comparé de nombreux paramètres entre eux pour permettre de quantifier l'eau et proposons celui qui nous semble le plus adapté pour quantifier les phases hydratés à la surface des petits corps sombres du Système Solaire. / Asteroids are relics from the early Solar System. Some of them are extremely primitive and can help in understanding the mechanic of Solar System formation, and ultimately the scenario that led to the formation of a habited planetary system. Reflectance spectroscopy is now a classical and useful method to analyze asteroid composition from the Earth or during space mission. In this PhD thesis, we tried to improve our understanding of the spectral properties of asteroids by looking at naturally delivered fragments, meteorites. We have used different analytical methods on carbonaceous chondrites (pieces of primitive asteroids) to characterized their chemical and mineralogical composition. We studied the nature of hydrated phases, water budget, phyllosilicate structures and the speciation of iron on these meteorites. All these analyses permit an improved understanding of the transformation of the mineralogy by parent body (asteroidal) alteration. Furthermore, these analyses provide quantitative and qualitative constraints to understand the factors controlling the reflectance measurement performed on the same meteorite. We compared different analytical parameters to quantify the water abundance and suggest a method to quantify hydrated phases on dark asteroids.

The discovery of Ni-, Cu-, and Zn-bearing Fe-sulfides from comet 81P/Wild 2 represents the strongest evidence, in the Stardust collection, of grains that formed in an aqueous environment. Crystalline sulfide assemblages from Wild 2 and the hydrothermally altered CI chondrite Orgueil were investigated. Structural and compositional characterizations of the sulfide grains from both collections reveal similarities. The Stardust samples include a cubanite (CuFe₂S₃) grain, a pyrrhotite [(Fe,Ni)₁₋ₓS]/pentlandite [(Fe,Ni)₉S₈] assemblage, and a pyrrhotite/sphalerite [(Fe,Zn)S] assemblage. Similarly, the CI-chondrite sulfides include individual cubanite and pyrrhotite grains, cubanite/pyrrhotite assemblages, pyrrhotite/pentlandite assemblages, as well as possible sphalerite inclusions within pyrrhotite grains. The cubanite is the low temperature orthorhombic form, which constrains temperature to a maximum of 210°C. The Stardust and Orgueil pyrrhotites are the 4C monoclinic polytype, which is not stable above ~250°C. The combinations of cubanite and pyrrhotite, as well as pyrrhotite and pentlandite, signify even lower temperatures. The crystal structures, compositions, and petrographic relationships of these sulfides constrain formation and alteration conditions. Taken together, these constraints attest to low-temperature hydrothermal processing. The hydrothermal conditions under which cubanite forms were investigated through thermodynamic modeling and experimental synthesis. A thermodynamic model for cubanite was developed to constrain its formation environment. Cubanite was synthesized under hydrothermal conditions consistent with those predicted for the CI-chondrite parent body. The similarity between Stardust and CI-chondrite sulfides suggest similar fluid conditions may have existed on the comet at some point in its history. The presence of cubanite in the Stardust collection has implications for large scale issues such as: heat sources in the comet-forming region; aqueous activity on cometary bodies; and the extent and mechanisms of radial mixing of material in the early nebula. The Wild 2 sulfides are most likely the products of low-temperature aqueous alteration and provide evidence of radial mixing of material from the inner solar system to the comet-forming region and possible secondary aqueous processing on the cometary body.

Volatiles are critical in understanding the history of the solar system. We conducted two case studies intended to further this understanding. First, we analyzed the presence of CO2 on Iapetus. Second, we evaluated aqueous alteration in CM chondrites.We studied the distribution, stability and production of CO2 on Saturn's moon Iapetus. We determined that CO2 is concentrated exclusively on Iapetus' dark material with an effective thickness of 31 nm. The total CO2 on Iapetus' surface is 2.3x108 kg. However, CO2 should not be present because it has a limited residence time on the surface of Iapetus. Our thermal calculations and modeling show that CO2 in the form of frost will not remain on Iapetus' surface beyond a few hundred years. Thus, it must be complexed with dark material. However, photodissociation will destroy the observed inventory in ~1/2 an Earth year.The lack of thermal and radiolytic stability requires an active source. We conducted experiments showing UV radiation generates CO2 under Iapetus-like conditions. We created a simulated regolith by mixing crushed water ice with isotopically labeled carbon. We then irradiated it with UV light at low temperature and pressure, producing 1.1x1015 parts m-2 s-1. Extrapolating to Iapetus, photolysis could generate 8.4x107 kg y-1, which makes photolytic production a good candidate for the source of the CO2 detected on Iapetus.We also studied the aqueous alteration of metal-bearing assemblages in CM chondrites. We examined Murchison, Cold Bokkeveld, Nogoya, and Murray using microscopy, electron microprobe analysis and scanning electron microscopy. Alteration on CM meteorites occurred within at least three microchemical environments: S-rich water, Si-rich water and water without substantial reactive components. Kamacite alters into tochilinite, cronstedtite, or magnetite. Sulfur associated alteration can form accessory minerals: P-rich sulfides, eskolaite and schreibersite.Additionally, we determined that there were two alteration events for some CM chondrites. The first formed a hydrated matrix prior to accretion, indicated by unaltered kamacite surrounded by a hydrated matrix. The second occurred after parent body formation. This event is indicated by large regions with consistent alteration features, surrounded by other regions of less altered material.

Chondritic meteorites are undifferentiated fragments of asteroids that contain the oldest solids formed in our Solar System. Their primitive, solar-like chemical compositions indicate that they experienced very little processing following accretion to their parent bodies. As such, they retain the best records of chemical and physical processes active in the protoplanetary disk during planet formation. Chondritic meteorites are depleted relative to the sun in volatile elements such as S and O. In addition to being important components of organic material, these elements exert a strong influence on the behavior of other more refractory species and the composition of planets. Understanding their distribution is therefore of key interest to the scientific community. While the bulk abundance of volatile elements in solid phases present in meteorites is below solar values, some meteorites record volatile-rich gas phases. The Rumuruti (R) chondrites record environments rich in both S and O, making them ideal probes for volatile enhancement in the early Solar System. Disentangling the effects of parent-body processing on pre-accretionary signatures requires unequilibrated meteorite samples. These samples are rare in the R chondrites. Here, I report analyses of unequilibrated clasts in two thin sections from the same meteorite, PRE 95404 (R3.2 to R4). Data include high resolution element maps, EMP chemical analyses from silicate, sulfide, phosphate, and spinel phases, SIMS oxygen isotope ratios of chondrules, and electron diffraction patterns from Cu-bearing phases. Oxygen isotope ratios and chondrule fO2 levels are consistent with type II chondrules in LL chondrites. Chondrule-sized, rounded sulfide nodules are ubiquitous in both thin sections. There are multiple instances of sulfide-silicate relationships that are petrologically similar to compound chondrules, suggesting that sulfide nodules and silicate chondrules formed as coexisting melts. This hypothesis is supported by the presence of phosphate inclusions and Cu-rich lamellae in both sulfide nodules and sulfide assemblages within silicate chondrules. Thermodynamic analyses indicate that sulfide melts reached temperatures up to 1138 °C and fS2 of 2 x 10^(-3) atm. These conditions require total pressures on the order of 1 atm, and a dust- or ice-rich environment. Comparison with current models suggest that either the environmental parameters used to model chondrule formation prior to planetesimal formation should be adjusted to meet this pressure constraint, or R chondrite chondrules may have formed through planetesimal bow shocks or impacts. The pre-accretionary environment recorded by unequilibrated R chondrites was therefore highly sulfidizing, and had fO2 higher than solar composition, but lower than the equilibrated R chondrites.Chalcopyrite is rare in meteorites, but forms terrestrially in hydrothermal sulfide deposits. It was previously reported in the R chondrites. I studied thin sections from PRE 95411 (R3 or R4), PCA 91002 (R3.8 to R5), and NWA 7514 (R6) using Cu X-ray maps and EMP chemical analyses of sulfide phases. I found chalcopyrite in all three samples. TEM electron diffraction data from a representative assemblage in PRE 95411 are consistent with this mineral identification. TEM images and X-ray maps reveal the presence of an oxide vein. A cubanite-like phase was identified in PCA 91002. Electron diffraction patterns are consistent with isocubanite. Cu-rich lamellae in the unequilibrated clasts of PRE 95404 are the presumed precursor materials for chalcopyrite and isocubanite. Diffraction patterns from these precursor phases index to bornite. I hypothesize that bornite formed during melt crystallization prior to accretion. Hydrothermal alteration on the parent body by an Fe-rich aqueous phase between 200 and 300°C resulted in the formation of isocubanite and chalcopyrite. In most instances, isocubanite may have transformed to chalcopyrite and pyrrhotite at temperatures below 210°C. This environment was both oxidizing and sulfidizing, suggesting that the R chondrites record an extended history of volatile-rich interaction. These results indicate that hydrothermal alteration of sulfides on the R chondrite parent body was pervasive and occurred even in low petrologic types. This high temperature aqueous activity is distinct from both the low temperature aqueous alteration of the carbonaceous chondrites and the high temperature, anhydrous alteration of the ordinary chondrites.

Ordinary chondrites are the most common type of meteorite to fall to Earth and are composed of lithified primitive nebular materials which have experienced variable extents of thermal metamorphism and shock processing. They were subjected to radiogenic heating by incorporation of unstable short lived radionuclides such as 26Al in the early solar system. The relationship between metamorphism and impact processing in ordinary chondrites is not fully understood. An unresolved issue in the study of ordinary chondrites is whether their original parent bodies were fragmented by impacts into rubble-pile bodies while they were still hot, or whether they retained their onion-shell structures until they had shed their radiogenic heat. Heat is lost more quickly due to catastrophic impacts because warm material from the interior is exposed directly to the space environment until the impact debris re-accretes into a rubble-pile body, and is then distributed evenly between the surface and the interior of the new rubble-pile body. The extent of retrograde metamorphism possible in ordinary chondrites would therefore largely be dictated by the extent to which their parent bodies were broken up by impacts. Disaggregation caused by an impact would record fast cooling between the temperature at the time of breakup and the temperature at the time of re-accretion. In this thesis project, five H6 chondrites (Butsura, Estacado, Kernouve, Portales Valley, Queen's Mercy) and five L6 chondrites (Bruderheim, Holbrook, Leedey, Morrow County, Park) were subjected to three different thermometry analyses (pyroxene, olivine spinel, and metallographic) to determine their cooling profiles and evaluate same set of samples. Cooling rates for pyroxene and olivine--spinel thermometry systems are determined using the formulation of Dodson (1973) as modified by Ganguly & Tirone (1999). Cooling rates for the metallographic system are determined using the method developed by Wood (1967) as modified by Willis & Goldstein (1981). At temperatures higher than ~600 degrees C, all samples experienced cooling rates which are orders of magnitude faster (100's to 1000's of degrees C/kyr) than what is predicted for onion--shell thermal evolution (10's of degrees C/Myr) by e.g. Monnereau et al. (2013). At temperatures below ~600 degrees C, i.e. those recorded by the metals, cooling rates are much slower in comparison to the silicate/oxide systems, with the exception of Park, which continued to cool quickly. The discrepancy between high-- and low--temperature cooling rates for both H-- and L--chondrites can best be accounted for by a catastrophic impact which occurred while each body was still near its peak metamorphic temperature, followed by re--accretion into a rubble--pile, which would then cool slowly due to the poor thermal conductivity of rubble--piles. Shock heating does not appear to affect silicate--oxide thermometers.

Relationships between organic molecules and inorganic minerals are investigated in five carbonaceous chondrites, Northwest Africa 852 (CR2), Tagish Lake (C2-ungroupped), Orgueil (CI1), Sutter's Mill (CM), and Murchison (CM2), with micron spatial resolution using synchrotron-based imaging micro-FTIR spectroscopy. Correlations based on absorption strength for various constituents are determined using statistical correlation analysis. Silicate band is found to be positively correlated with stretching modes of aliphatic hydrocarbons in NWA 852 and Tagish Lake. The former is highly correlated with the hydration band in all meteorites. Negative correlation is observed between water+organics and carbonate bands in all meteorites. Two dimensional infrared maps for NWA 852 and Orgueil show that carbonates are spatially separated from water+organic combination, silicates, OH, and CH distributions. Overlapping of the latter three in NWA 852 and Tagish Lake suggests a possible catalytic role of phyllosilicates in the formation of organics. Additionally, spectroscopic analyses on Sutter's Mill meteorite fragments present multiple distinct mineralogies. Spatial and spectral evidences on this regolith breccia suggest mixing of multiple parent bodies. Ratios of asymmetric CH2 and CH3 band strengths for NWA 852, Tagish Lake, and Sutter's Mill are similar to the average ratio of interplanetary dust particles and Wild 2 cometary dust particles, however significantly exceeds that of interstellar medium objects and several aqueously altered carbonaceous chondrites such as Orgueil. This suggests distinct formation regions and/or parent body processing of organics for these meteorites. Our infrared spectro-microtomography measurements on Murchison meteorite, representing the first such measurement on any kind of meteorite, comprise of three-dimensional reconstructions of specific molecular functional groups for understanding the spatial distributions of these groups.

Analyzing the constituents of meteorites has played an important role in forming the contemporary theories of solar system evolution, planets formation, and stellar evolution. Meteorites are often a complex mixture of common rock forming silicates, such as olivines and pyroxenes, with a range of exotic species including hydrated silicates, and in some cases organic compounds. We used Micro-Raman spectroscopy to analyze the compositions of three carbonaceous chondrites: NWA852, Murchison and Allende. Raman spectra were measured using laser sources with different excitation wavelengths: HeNe 633 nm and Nd:YAG 532 nm. We were able to detect 9 minerals in NWA852, 3 minerals in Murchison and 4 minerals in Allende. Some of these minerals like pyrite in NWA852 and magnetite in NWA852 and Murchison provide evidence for potential previous organic life. Other minerals like ringwoodite in Allende and lizardite in NWA852 reveal information about previous astrophysical and geological events experienced by the meteorites. The detection of graphite in the Murchison and Allende reveals information about the microstructure of these meteorites.

Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Earth and Planetary Science, 1980. / Microfiche copy available in Archives and Science. / Bibliography: leaves 77-80. / by Dushan Stephen Bukvic. / M.S.

La formation des planètes a laissé derrière elle des matériaux dont la nature primordiale a été préservée. Ces astéroïdes primitifs de la ceinture principale sont aujourd'hui échantillonnés par la diversité de météorites chondritiques dans nos collections qui nous permettent d'étudier les premiers instants du Système Solaire. Cependant, beaucoup d'entre elles présentent des traces d'altération hydrothermale qui ont modifié leur minéralogie, et ainsi occulté ces informations primordiales. Ce processus de modification de la roche via l'interaction avec un fluide a été grandement étudié au cours des dernières décennies, notamment dans les chondrites carbonées de type CM, dont la minéralogie témoigne de plusieurs épisodes d'altération dans différents degrés d'intensité. Comprendre l'évolution de l'eau ainsi que l'influence de ce processus sur la matière organique dans ces astéroïdes est essentiel du fait de leur éventuelle contribution à l'origine de la vie sur Terre. Afin de mieux contraindre les conditions géochimique et chronologique dans lesquelles est survenu ce processus, les travaux de cette thèse ont été focalisés sur les chondrites de type CM et les phases secondaires qu'ils contiennent. Des mesures in situ des isotopes de l'oxygène dans les carbonates des CM nous ont permis de développer une méthode d'estimation de leurs températures de précipitation. Nos résultats indiquent une gamme de températures bien plus étendue que celles estimées auparavant, s'étalant de -50 à environ 300 °C avec une température moyenne de 113 +/- 54°C (2σ). Afin d'approfondir notre étude des conditions géochimiques de l'altération nous avons conduit une étude détaillée de la chondrite de Boriskino. La texture atypique de cette chondrite, due à ses nombreux clastes aux frontières nettes et aux degrés d'altération variables, nous a permis d'explorer l'hypothèse d'un lien entre les processus à l'origine de la formation des brèches et l'altération hydrothermale. L'utilisation de notre nouvelle méthode sur les carbonates de cette chondrite a mis en évidence un rôle secondaire de la température dans l'intensité du processus d'altération. De plus, nos travaux suggèrent que les épisodes d'altération sont antérieurs à la formation du corps-parent final et que la quantité de glace initialement accrétée peut être le facteur dominant de l'efficacité du processus d'altération. Néanmoins cette hypothèse ne prend pas en compte l'influence que peut avoir la durée d'exposition de la roche au fluide. Afin de tester cette dernière hypothèse, notre dernier projet devait permettre d'estimer l'âge des carbonates dans des CM présentant différents degrés d'altération. La datation de ces objets repose sur la décroissance radioactive du radioisotope 53Mn en 53Cr. Cependant, l'absence de standards de carbonates adéquats pour ces mesures nous a conduit dans un premier temps à les synthétiser. Pour ce faire nous avons abordé le problème en nous éloignant des méthodes traditionnelles de précipitation de carbonates sur substrat ayant conduit à des minéraux très hétérogènes, et nous avons effectué nos synthèses à haute pression et haute température grâce à une presse piston-cylindre. / Chondrites are leftover solids from the evolution of the solar protoplanetary disk that enable for its primordial conditions to be studied. However, many chondrites have seen their mineralogy modified by the circulation of fluids during hydrothermal alteration events, thereby blurring the primordial informations retained in it. CM carbonaceous chondrites have been extensively studied, mainly because of the various episodes and extent of hydrothermal alteration they exhibit. The understanding of the evolution of water and the influence of alteration on organic matter in those asteroids is essential as they might be the source of life on Earth. In order to better understand the geochemical conditions and the chronology of this process in carbonaceous asteroids, we focused this project on CM chondrites and the secondary phases they contain. We developped a methodology to estimate the precipitation temperatures of carbonates in CM chondrites relying only on in situ measurements of their O-isotopic composition. Our results yield precipitation temperatures in a larger range than what has previsouly been estimated, i.e. from -50 to approximatively 300°C with an average temperature of 113 +/- 54°C (2σ). To further our study of the geochemical conditions of hydrothermal alteration we extensively studied the CM of Boriskino. The peculiar texture of this meteorite, due to its numerous clasts with sharp boundaries and their various degrees of aqueous alteration, enable to investigate the reccurent question of a genetic link between brecciation and aqueous alteration. Using the same methodology as in our first project we concluded that temperatures in which the process took place could not account for the various extent of aqueous alteration that we observe. In addition, Our work suggest that aqueous alteration in this chondrite was discontinuous and preceeded brecciationand that instead the initial quantity of accreted ice could be the controlling parameter of aqueous alteration. However, this study neglect the contribution of the duration of exposure of the rock to the fluid to the extent of aqueous alteration. Therefore, our last project was to determine the age of carbonates in several CM chondrites of various degrees of aqueous alteration. The datation of these minerals in chondrites relies on the radiochronometer 53Mn-53Cr. However, the lack of a suitable carbonate standard for these SIMS analyses pushed us to synthetize carbonates with the adequat cristallinity and chemical composition first. To do so, we experimentated at high pressure and high temperature using a piston-cylinder apparatus.