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The solar oxygen‐isotopic composition: Predictions and implications for solar nebula processes
Author(s) -
WIENS R. C.,
HUSS G. R.,
BURNETT D. S.
Publication year - 1999
Publication title -
meteoritics and planetary science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.09
H-Index - 100
eISSN - 1945-5100
pISSN - 1086-9379
DOI - 10.1111/j.1945-5100.1999.tb01735.x
Subject(s) - formation and evolution of the solar system , chondrite , meteorite , solar system , chemical composition , gas composition , composition (language) , presolar grains , ordinary chondrite , carbonaceous chondrite , mineralogy , analytical chemistry (journal) , astrophysics , astrobiology , chemistry , physics , thermodynamics , environmental chemistry , linguistics , philosophy
— The outer layers of the Sun are thought to preserve the average isotopic and chemical composition of the solar system. The solar O‐isotopic composition is essentially unmeasured, though models based on variations in meteoritic materials yield several predictions. These predictions are reviewed and possible variations on these predictions are explored. In particular, the two‐component mixing model of Clayton and Mayeda (1984) (slightly revised here) predicts solar compositions to lie along an extension of the calcium‐aluminum‐rich inclusion (CAI) 16 O line between (δ 18 O, δ 17 O) = (16.4, 11.4)%0 and (12.3, 7.5)%0. Consideration of data from ordinary chondrites suggests that the range of predicted solar composition should extend to slightly lower δ 18 O values. The predicted solar composition is critically sensitive to the solid/gas ratio in the meteorite‐forming region, which is often considered to be significantly enriched over solar composition. A factor of two solid/gas enrichment raises the predicted solar (δ 18 O, δ 17 O) values along an extension of the CAI 16 O line to (33, 28)%0. The model is also sensitive to the nebular O gas phase. If conversion of most of the gaseous O from CO to H 2 O occurred at relatively low temperatures and was incomplete at the time of CM aqueous alteration, the predicted nebular gas composition (and hence the solar composition) would be isotopically heavier along a slope 1/2 line. The likelihood of having a single solid nebular O component is discussed. A distribution of initial solid compositions along the CAI 16 O line (rather than simply as an end‐member) would not significantly change the predictions above in at least one scenario. Even considering these variations within the mixing model, the predicted range of solar compositions is distinct from that expected if the meteoritic variations are due to non‐mass‐dependent fractionation. Thus, a measurement of the solar O composition to a precision of several permil would clearly distinguish between these theories and should clarify a number of other important issues regarding solar system formation.