Masanao Abe

Abstract Understanding the processes of aqueous alteration within primitive bodies is crucial for unraveling the complex history of early planetesimals. To better identify the signs of this process and its consequences, we have studied the heterogeneity at a micrometric scale of the structure of the aliphatic organic compounds and its relationship to its mineralogical environment. Here, we report an analysis performed on two micrometric grains of Ryugu (C0002‐FC027 and C0002‐FC028). The samples were crushed in a diamond compression cell and analyzed using high‐spatial resolution Fourier Transform InfraRed (FT‐IR) hyperspectral imaging measurements conducted in transmission mode. We showed here the spatial distributions of the main components and the structural heterogeneity of the aliphatic organic matter highlighting a micrometer‐scale variability in the methylene‐to‐methyl ratio. Moreover, we connected this heterogeneity to the one of the phyllosilicate band positions. Our findings indicate that the organic matter within Ryugu's micrometric grains underwent varying degrees of aqueous alteration in distinct microenvironments resulting in an elongation of the length of their aliphatic chains, and/or a reduction in their branching and/or cross‐linking.

Abstract Nucleosynthetic isotope variations are powerful tracers to determine genetic relationships between meteorites and planetary bodies. They can help to link material collected by space missions to known meteorite groups. The Hayabusa 2 mission returned samples from the Cb‐type asteroid (162173) Ryugu. The mineralogical, chemical, and isotopic characteristics of these samples show strong similarities to carbonaceous chondrites and in particular CI chondrites. The nucleosynthetic isotope compositions of Ryugu overlap with CI chondrites for several elements (e.g., Cr, Ti, Fe, and Zn). In contrast to these isotopes, which are of predominately supernovae origin, s‐process variations in Mo isotope data are similar to those of carbonaceous chondrites, but even more s‐process depleted. To further constrain the origin of this depletion and test whether this signature is also present for other s‐process elements, we report Zr isotope compositions for three bulk Ryugu samples (A0106, A0106‐A0107, C0108) collected from the Hayabusa 2 mission. The data are complemented with that of terrestrial rock reference materials, eucrites, and carbonaceous chondrites. The Ryugu samples are characterized by distinct ⁹⁶Zr enrichment relative to Earth, indicative of a s‐process depletion. Such depletion is also observed for carbonaceous chondrites and eucrites, in line with previous Zr isotope work, but it is more extreme in Ryugu, as observed for Mo isotopes. Since s‐process Zr and Mo are coupled in mainstream SiC grains, these distinct s‐process variations might be due to SiC grain depletion in the analyzed materials, potentially caused by incomplete sample digestion, because the Ryugu samples were dissolved on a hotplate only to avoid high blank levels for other elements (e.g., Cr). However, local depletion of SiC grains cannot be excluded. An alternative, equally possible scenario is that aqueous alteration redistributed anomalous, s‐process‐depleted, Zr on a local scale, for example, into Ca‐phosphates or phyllosilicates.