Abstract
Since the first discovery of extraordinary oxygen isotope compositions in carbonaceous meteorites by Clayton et al. [Clayton, R.N., Grossman, L., Mayeda, T.K., 1973. Science 182, 485–488], numerous studies have been done to explain the unusual mass-independent isotope fractionation, but the problem is still unresolved to this day. Clayton's latest interpretation [Clayton, R.N., 2002. Nature 415, 860–861] sheds new light on the problem, and possible hypotheses now seem to be fairly well defined. A key issue is to resolve whether the oxygen isotopes in the Solar System represented by the Sun (solar oxygen) are the same as oxygen isotopes in planetary objects such as bulk meteorites, Mars, Earth, and Moon, or whether the solar oxygen is more similar to the lightest oxygen isotopes observed in CAIs (Calcium Aluminum-rich Inclusions) in primitive meteorites. Here, we examined the problem using oxygen isotope analytical data of about 400 bulk meteorite samples of various classes or types (data compiled by K. Lodders). We used in our discussion exclusively the parameter ΔO17, a direct measure of the degree of mass-independent isotope fractionation of oxygen isotopes. When ΔO17 is arranged according to a characteristic size of their host planetary object, it shows a systematic trend: (1) ΔO17 values scatter around zero; (2) the scatter from the mean (ΔO17=0) decreases with increasing representative size of the respective host planetary object. This systematic trend is easily understood on the basis of a hierarchical scenario of planetary formation, that is, larger planetary objects have formed by progressive accretion of planetesimals by random sampling over a wide spectrum of proto-solar materials. If this progressive random sampling of planetesimals were the essential process of planetary formation, the isotopic composition of planetary oxygen should approach that of the solar oxygen. To test this random sampling hypothesis, we applied a multiscale, multistep bootstrap statistical method [Shimodaira, H., 2004. Ann. Statist. 32, 2616–2641] to the meteorite oxygen isotope data, and deduced a σ–N relation, where σ is the standard deviation of ΔO17, and N is the representative size of a host planetary object. If we assign 200 and 500 km as a representative sizes of the chondrite and achondrite parent bodies, the observed σ of ΔO17 agree well with the values predicted by the σ–N relation. A common mean value of ΔO17=0 for all planetary objects also agrees with the progressive random sampling process. Therefore, we conclude that the solar oxygen is the same as planetary oxygen, but differs from CAI oxygen. The conclusion implies that a massive enrichment in 17O and 18O resulting from CO self-shielding, a current influential interpretation of CAI-O, did not occur.
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