Accretion and Preservation of Organic Matter in Carbonaceous Chondrites as Revealed by NanoSIMS Imaging.

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1060 Planetary Geochemistry (5405, 5410, 5704, 5709, 6005, 6008), 3617 Alteration And Weathering Processes (1039), 3662 Meteorite Mineralogy And Petrology (1028, 6240), 6213 Dust, 6240 Meteorites And Tektites (1028, 3662)

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Carbonaceous chondrites are the most primitive known meteorites. Their parent bodies accreted several discrete components of the early solar system: CAIs, other silicates, oxides, sulfides, ice, organics, and noble gases. Radioactive decay of short live radionucleides quickly heated these parent bodies and drove thermal metamorphism and aqueous alteration of their constituents. Despite this post-acretionary modification, at least some components of the organic matter in the carbaceous chondrites retained distinctive isotopic and molecular properties that may relate to their pre-acretionary origins in the protosolar nebula or in the molecular cloud that gave birth to it [1]. These processes that gave rise to early solar-system organic matter and the extent to which it was modified by parent body processes are still a matter of debate [2]. We have acquired NanoSIMS images of matrices of several CI, CM, CR and CV chondrites to document, in- situ, the distribution of organics and their textural and chemical relationships to co-existing inorganic components. Importantly, we performed these analyses on essentially unmodified fragments of matrix material pressed into indium, rather than on extracts, which have been the focus of most previous work on meteoritic organic matter. Specifically, we simultaneously collected H, D, 12C, 18O, 26CN, 28Si and 32S with a spatial resolution of 200 nm. Inorganic constituents of the imaged domains were determined by SEM imaging and EDS analysis. We identify two textural classes of organic constituents: diffuse organic matter and organic particles ~ 1 micron in diameter. The particles are common and do not exhibit any textural association with any inorganic matrix constituent. This distribution is consistent with previous observations by fluorescence optical microscopy [3]. These organic particles are likely primarily composed of insoluble organic matter (IOM) that grew prior to accretion as pure organic particules and was preserved in the matrix. In contrast to some observations of nm-scale HRTEM observations of chondritic matrices [4], organics do not seem to be associated with sulfides or sulfates. Instead, they are found intermixed with clay minerals within the matrix. We also found that a subset of organic particles in the matrices of CI, CM and CR chondrites are D rich (as previously reported by [5]). Profiles across these particles reveal that no significant isotopic exchange has occurred between these D-rich organic grains and the surrounding clays. This suggests that the isotopic composition of these grains remained unchanged during the parent body evolution, in contrast with conclusions from bulk measurements [2]. It has been previously suggested that relatively D-depleted water circulated through the parent bodies of the volatile-rich carbonaceous chondrites for 3 My. Known rates of water mobility through polymerized organic compounds and of D/H exchange between organic hydrogen and water lead one to predict that organic particles should have fully equilibrated with their surrounding phases in much less time than this. We speculate that this paradox might be evidence for exceptionally refractory character of H-C bonds in meteoritic IOM, or extreme D-exchange behavior of some organic moieties like radicals evidenced in IOM. [1] Pizzarello et al. (2006) in MESS II 625-651; [2] Alexander et al. (2007) GCA 71, 4380-4403 ; [3] Alpern and Benkheiri (1973) EPSL 19, 422-428; [4] Brearley and Abreu 32th LPSC; [5] Busemann et al (2006) Science 312, 727-730.

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