A framework for predicting global silicate weathering and CO2 drawdown rates over geologic time-scales

  1. George E. Hilleya,1 and
  2. Stephen Porderb
  1. aDepartment of Geological and Environmental Sciences, Stanford University, Stanford, CA 94062; and
  2. bDepartment of Ecology and Evolutionary Biology, Brown University, Providence, RI 02912
  1. Edited by Robert A. Berner, Yale University, New Haven, CT, and approved August 27, 2008 (received for review February 15, 2008)

Abstract

Global silicate weathering drives long-time-scale fluctuations in atmospheric CO2. While tectonics, climate, and rock-type influence silicate weathering, it is unclear how these factors combine to drive global rates. Here, we explore whether local erosion rates, GCM-derived dust fluxes, temperature, and water balance can capture global variation in silicate weathering. Our spatially explicit approach predicts 1.9–4.6 × 1013 mols of Si weathered globally per year, within a factor of 4–10 of estimates of global silicate fluxes derived from riverine measurements. Similarly, our watershed-based estimates are within a factor of 4–18 (mean of 5.3) of the silica fluxes measured in the world's ten largest rivers. Eighty percent of total global silicate weathering product traveling as dissolved load occurs within a narrow range (0.01–0.5 mm/year) of erosion rates. Assuming each mol of Mg or Ca reacts with 1 mol of CO2, 1.5–3.3 × 108 tons/year of CO2 is consumed by silicate weathering, consistent with previously published estimates. Approximately 50% of this drawdown occurs in the world's active mountain belts, emphasizing the importance of tectonic regulation of global climate over geologic timescales.

Footnotes

  • 1To whom correspondence should be addressed. E-mail: hilley{at}stanford.edu
  • Author contributions: G.E.H. and S.P. designed research; G.E.H. and S.P. performed research; G.E.H. contributed new reagents/analytic tools; G.E.H. and S.P. analyzed data; and G.E.H. and S.P. wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0801462105/DCSupplemental.

  • Freely available online through the PNAS open access option.

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