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Letters to Nature
Nature 408, 951-954 (21 December 2000) | doi:10.1038/35050058; Received 20 June 2000; Accepted 6 November 2000
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Endowed Professorship
- Washington University School of Medicine in St. Louis
- St. Louis, MO 63110 United States
Faculty - Plant Cellular & Molecular Biology, Molecular Genetics & the Plant Molecular Biology / Biotechnology Program
- The Ohio State University
- Columbus, Ohio
The influence of rivers on marine boron isotopes and implications for reconstructing past ocean pH
D. Lemarchand, J. Gaillardet, É. Lewin & C. J. Allègre
- Laboratoire de Géochimie et Cosmochimie, Institut de Physique du globe de Paris, 4 place Jussieu, 75252 Paris Cedex 05
Correspondence to: D. Lemarchand Correspondence and requests for materials should be addressed to D.L. (e-mail: Email: lemarcha@ipgp.jussieu.fr).
Abstract
Ocean pH is particularly sensitive to atmospheric carbon dioxide content1, 2, 3. Records of ocean pH can therefore be used to estimate past atmospheric carbon dioxide concentrations. The isotopic composition of boron (
11B) contained in the carbonate shells of marine organisms varies according to pH, from which ocean pH can be reconstructed4, 5, 6, 7, 8, 9, 10, 11. This requires independent estimates of the
11B of dissolved boron in sea water through time. The marine
11B budget, however, is still largely unconstrained. Here we show that, by incorporating the global flux of riverine boron (as estimated from
11B measurements in 22 of the world's main rivers), the marine boron isotope budget can be balanced. We also derive ocean
11B budgets for the past 120 Myr. Estimated isotope compositions of boron in sea water show a remarkable consistency with records of
11B in foraminiferal carbonates9, 10, 11, suggesting that foraminifera
11B records may in part reflect changes in the marine boron isotope budget rather than changes in ocean pH over the Cenozoic era.
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