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Abstract The calcium–aluminum-rich inclusions (CAIs) from chondritic meteorites are the first solids formed in the solar system. Rim formation around CAIs marks a time period in early solar system history when CAIs existed as free-floating objects and had not yet been incorporated into their chondritic parent bodies. The chronological data on these rims are limited. As seen in the limited number of analyzed inclusions, the rims formed nearly contemporaneously (i.e., <300,000 yr after CAI formation) with the host CAIs. Here we present the relative ages of rims around two type B CAIs from NWA 8323 CV3 (oxidized) carbonaceous chondrite using the 26 Al– 26 Mg chronometer. Our data indicate that these rims formed ∼2–3 Ma after their host CAIs, most likely as a result of thermal processing in the solar nebula at that time. Our results imply that these CAIs remained as free-floating objects in the solar nebula for this duration. The formation of these rims coincides with the time interval during which the majority of chondrules formed, suggesting that some rims may have formed in transient heating events similar to those that produced most chondrules in the solar nebula. The results reported here additionally bolster recent evidence suggesting that chondritic materials accreted to form chondrite parent bodies later than the early-formed planetary embryos, and after the primary heat source, most likely 26 Al, had mostly decayed away. 

Asteroid Ryugu and Ivuna-type carbonaceous meteorites may have originated from the outskirts of the Solar System. 

Abstract Oxygen 3‐isotope ratios of magnetite and carbonates in aqueously altered carbonaceous chondrites provide important clues to understanding the evolution of the fluid in the asteroidal parent bodies. We conducted oxygen 3‐isotope analyses of magnetite, dolomite, and breunnerite in two sections of asteroid Ryugu returned samples, A0058 and C0002, using a secondary ion mass spectrometer (SIMS). Magnetite was analyzed by using a lower primary ion energy that reduced instrumental biases due to the crystal orientation effect. We found two groups of magnetite data identified from the SIMS pit morphologies: (1) higher δ¹⁸O (from 3‰ to 7‰) and ∆¹⁷O (~2‰) with porous SIMS pits mostly from spherulitic magnetite, and (2) lower δ¹⁸O (~ −3‰) and variable ∆¹⁷O (0‰–2‰) mostly from euhedral magnetite. Dolomite and breunnerite analyses were conducted using multi‐collection Faraday cup detectors with precisions ≤0.3‰. The instrumental bias correction was applied based on carbonate compositions in two ways, using Fe and (Fe + Mn) contents, respectively, because Ryugu dolomite contains higher amounts of Mn than the terrestrial standard. Results of dolomite and breunnerite analyses show a narrow range of ∆¹⁷O; 0.0‰–0.3‰ for dolomite in A0058 and 0.2‰–0.8‰ for dolomite and breunnerite in C0002. The majority of breunnerite, including large ≥100 μm grains, show systematically lower δ¹⁸O (~21‰) than dolomite (25‰–30‰ and 23‰–27‰ depending on the instrumental bias corrections). The equilibrium temperatures between magnetite and dolomite from the coarse‐grained lithology in A0058 are calculated to be 51 ± 11°C and 78 ± 14°C, depending on the instrumental bias correction scheme for dolomite; a reliable temperature estimate would require a Mn‐bearing dolomite standard to evaluate the instrumental bias corrections, which is not currently available. These results indicate that the oxygen isotope ratios of aqueous fluids in the Ryugu parent asteroid were isotopically heterogeneous, either spatially, or temporary. Initial water ice accreted to the Ryugu parent body might have ∆¹⁷O > 2‰ that was melted and interacted with anhydrous solids with the initial ∆¹⁷O < 0‰. In the early stage of aqueous alteration, spherulitic magnetite and calcite formed from aqueous fluid with ∆¹⁷O ~ 2‰ that was produced by isotope exchange between water (∆¹⁷O > 2‰) and anhydrous solids (∆¹⁷O < 0‰). Dolomite and breunnerite, along with some magnetite, formed at the later stage of aqueous alteration under higher water‐to‐rock ratios where the oxygen isotope ratios were nearly at equilibrium between fluid and solid phases. Including literature data, δ¹⁸O of carbonates decreased in the order calcite, dolomite, and breunnerite, suggesting that the temperature of alteration might have increased with the degree of aqueous alteration.