LOW-TEMPERATURE AQUEOUS ALTERATION ON THE CR CHONDRITE PARENT BODY: IMPLICATIONS FROM IN SITU OXYGEN-ISOTOPE ANALYSES

1,2Christine E. Jilly-Rehak, 2Gary R. Huss, 2Kazu Nagashima, 3Devin L. Schrader
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2017.10.007]
1Department of Geology & Geophysics, University of Hawai‘i at Mānoa, 1680 East-West Rd. POST 517A, Honolulu HI 96822, USA
2Hawai‘i Institute of Geophysics and Planetology, University of Hawai‘i at Mānoa, 1680 East-West Rd. POST 602, Honolulu HI 96822, USA
3Center for Meteorite Studies, School of Earth and Space Exploration, Arizona State University, PO Box 871404, Tempe AZ 85287, USA
Copyright Elsevier

The presence of hydrated minerals in chondrites indicates that water played an important role in the geologic evolution of the early Solar System; however, the process of aqueous alteration is still poorly understood. Renazzo-like carbonaceous (CR) chondrites are particularly well-suited for the study of aqueous alteration. Samples range from being nearly anhydrous to fully altered, essentially representing snapshots of the alteration process through time. We studied oxygen isotopes in secondary-minerals from six CR chondrites of varying hydration states to determine how aqueous fluid conditions (including composition and temperature) evolved on the parent body. Secondary minerals analyzed included calcite, dolomite, and magnetite. The O-isotope composition of calcites ranged from δ18O ≈ 9 to 35 ‰, dolomites from δ18O ≈ 23 to 27 ‰, and magnetites from δ18O ≈ -18 to 5 ‰. Calcite in less-altered samples showed more evidence of fluid evolution compared to heavily altered samples, likely reflecting lower water/rock ratios. Most magnetite plotted on a single trend, with the exception of grains from the extensively hydrated chondrite MIL 090292. The MIL 090292 magnetite diverges from this trend, possibly indicating an anomalous origin for the meteorite. If magnetite and calcite formed in equilibrium, then the relative 18O fractionation between them can be used to extract the temperature of co-precipitation. Isotopic fractionation in Al Rais carbonate-magnetite assemblages revealed low precipitation temperatures (∼60°C). Assuming that the CR parent body experienced closed-system alteration, a similar exercise for parallel calcite and magnetite O-isotope arrays yields “global” alteration temperatures of ∼55 to 88 °C. These secondary mineral arrays indicate that the O-isotopic composition of the altering fluid evolved upon progressive alteration, beginning near the Al Rais water composition of Δ17O ∼ 1 ‰ and δ18O ∼ 10 ‰, and becoming increasingly 16O-enriched toward a final fluid composition of Δ17O ∼ -1.2 ‰ and δ18O ∼ -15 ‰.

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