2020) Potassium isotope compositions of carbonaceous and ordinary chondrites: Implications on the origin of volatile depletion in the early solar system. Geochimica et Cosmochimica Acta, in press. ABSTRACT Among solar system materials there are variable degrees of depletion in moderately volatile elements (MVEs, such as Na, K, Rb, Cu, and Zn) relative to the proto-solar composition. Whether these depletions are due to nebular and/or parent-body (asteroidal or planetary) processes is still under debate. In order to help decipher the MVE abundances in early solar system materials, we conducted a systematic study of highprecision K stable isotopic compositions of a suite of whole-rock samples of wellcharacterized carbonaceous and ordinary chondrites. We analyzed 16 carbonaceous chondrites (CM1-2, CO3, CV3, CR2, CK4-5 and CH3) and 28 ordinary chondrites covering petrological types 3 to 6 and chemical groups H, L, and LL. We observed significant K isotope (δ 41 K) variations (−1.54 to 0.70 ‰) among the carbonaceous and ordinary chondrites. In general, the two major chondrite groups are distinct: The K isotope compositions of carbonaceous chondrites are largely higher than the Bulk Silicate Earth (BSE) value, whereas ordinary chondrites show K isotope compositions that are typically lower than the BSE value. Neither carbonaceous nor ordinary chondrites show clear/resolvable correlations between K isotopes and chemical groups, petrological types, shock levels, cosmic-ray exposure ages, fall/find occurrence, or terrestrial weathering. Importantly, the lack of a clear trend between K isotopes and K content among chondrites indicates that the K isotope fractionations were decoupled from the relative elemental K depletions, which is inconsistent with a single-stage partial vaporization or condensation process to account for these MVE depletion patterns among chondrites. The range of K isotope variations in the carbonaceous chondrites in this study is consistent with a fourcomponent (chondrule, refractory inclusion, matrix and water) mixing model that is able to explain the bulk elemental and isotopic compositions of the main carbonaceous chondrite groups, but requires a fractionation in K isotopic compositions in chondrules.We propose that the major control of the isotopic compositions of group averages is condensation and/or vaporization in pre-accretional (nebular) environments that is preserved in the compositional variation of chondrules. Parent-body processes, such as aqueous alteration, thermal metamorphism, and metasomatism, can mobilize K and affect the K isotopes in individual samples. In the case of the ordinary chondrites, the full range of K isotopic variations can only be explained by the combined effects of the size and relative abundances of chondrules, parent-body aqueous and thermal alteration, and possible sampling bias.compositions between different planetary materials (e.g., Earth and Moon) that were subsequently used to better understand the accretion mechanism of different planetary bodies.

The abundances of water and highly to moderately volatile elements in planets are considered critical to mantle convection, surface evolution processes, and habitability. From the first flyby space probes to the more recent “Perseverance” and “Tianwen-1” missions, “follow the water,” and, more broadly, “volatiles,” has been one of the key themes of martian exploration. Ratios of volatiles relative to refractory elements (e.g., K/Th, Rb/Sr) are consistent with a higher volatile content for Mars than for Earth, despite the contrasting present-day surface conditions of those bodies. This study presents K isotope data from a spectrum of martian lithologies as an isotopic tracer for comparing the inventories of highly and moderately volatile elements and compounds of planetary bodies. Here, we show that meteorites from Mars have systematically heavier K isotopic compositions than the bulk silicate Earth, implying a greater loss of K from Mars than from Earth. The average “bulk silicate” δ41K values of Earth, Moon, Mars, and the asteroid 4-Vesta correlate with surface gravity, the Mn/Na “volatility” ratio, and most notably, bulk planet H2O abundance. These relationships indicate that planetary volatile abundances result from variable volatile loss during accretionary growth in which larger mass bodies preferentially retain volatile elements over lower mass objects. There is likely a threshold on the size requirements of rocky (exo)planets to retain enough H2O to enable habitability and plate tectonics, with mass exceeding that of Mars.

Enstatite chondrites and aubrites are meteorites that show the closest similarities to the Earth in many isotope systems that undergo mass-independent and mass-dependent isotopic fractionations. Due to the analytical challenges to obtain high-precision K isotopic compositions in the past, potential differences in K isotopic compositions between enstatite meteorites and the Earth remained uncertain. We report the first high-precision K isotopic compositions of eight enstatite chondrites and four aubrites and find that there is a significant variation of K isotopic compositions among enstatite meteorites (from −2.34‰ to −0.18‰). However, K isotopic compositions of nearly all enstatite meteorites scatter around the Bulk Silicate Earth (BSE) value. The average K isotopic composition of the eight enstatite chondrites (−0.47 ±0.57‰) is indistinguishable from the BSE value (−0.48 ±0.03‰), thus further corroborating the isotopic similarity between Earth' building blocks and enstatite meteorite precursors. We found no correlation of K isotopic compositions with the chemical groups, petrological types, shock degrees, and terrestrial weathering conditions; however, the variation of K isotopes among enstatite meteorite can be attributed to the parent-body processing. Our sample of the main-group aubrite MIL 13004 is exceptional and has an extremely light K isotopic composition (δ 41 K=−2.34 ±0.12‰). We attribute this unique K isotopic feature to the presence of abundant djerfisherite inclusions in our sample because this K-bearing sulfide mineral is predicted to be enriched in 39 K during equilibrium exchange with silicates.