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Rumurutiites (R chondrites) are rare, highly oxidized chondrites belonging to the noncarbonaceous superclan and characterized by low chondrule abundances. Although textural and chemical features of Rumurutiite chondrules resemble those of ordinary chondrites (OCs), their formation conditions and potential genetic link remain debated. Here, we report high-resolution elemental X-ray mapping analyses and in situ O isotopic measurements of olivine grains from five chondrules and eight isolated olivine grains (IOGs) in the NWA 12482 R3 chondrite. The chondrules show chemical zonings similar to their counterparts in ordinary and carbonaceous chondrites (CCs), implying that gas-melt interaction processes between chondrule precursors and SiO-and Mg-rich gas were operative throughout the circumsolar disk. Our isotopic data show that R chondrules are isotopically similar to ordinary chondrules, although differences in their abundances of relict olivine grains and chondrule textural characteristics suggest different formation environments, with R chondrules being formed from 16 O-poorer precursors. As with chondrules in OCs, the O isotopic characteristics of R chondrules and IOGs suggest limited transport between CC and noncarbonaceous reservoirs.

In carbonaceous chondrites, Mg‐spinel (MgAl2O4) grains are ubiquitous in refractory inclusions but rarely reported in chondrules, where they may correspond to minerals either (i) inherited from chondrule precursors or (ii) crystallized from chondrule melts. Here, we report high‐current quantitative electron microprobe measurements and secondary ion mass spectrometry oxygen isotopic analyses of Mg‐spinel‐bearing chondrules in the CV3 carbonaceous chondrites Northwest Africa 10235 and Allende. Compared to spinels in refractory inclusions, chondrule spinels are characterized by higher Cr contents and 16O‐poorer oxygen isotopic signatures (∆17O ≡ δ17O−0.52 × δ18O, from −2 to −6‰). Because the similar Δ17O values of chondrule olivine and spinel crystals imply their comagmatic origin, we applied a geothermometer based on the Al‐Cr distribution between these minerals to determine their crystallization temperatures. The calculated temperatures range from 1200 to 1640 °C (mean = 1470 °C), most being lower than the estimated liquidus temperature of porphyritic chondrules (~1600 °C). Our results suggest that chondrules experienced relatively slow cooling rates (slower than a few hundreds of °C h−1), which is in good agreement with models of chondrule formation invoking nonlinear or two‐stage cooling rates.

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