Impact of anthropogenic atmospheric nitrogen and sulfur deposition on ocean acidification and the inorganic carbon system

  1. Scott C. Doney*,,
  2. Natalie Mahowald,
  3. Ivan Lima*,
  4. Richard A. Feely§,
  5. Fred T. Mackenzie,
  6. Jean-Francois Lamarque, and
  7. Phil J. Rasch
  1. *Marine Chemistry and Geochemistry Department, Woods Hole Oceanographic Institution, 266 Woods Hole Road, Woods Hole, MA 02543;
  2. Divisions of Climate and Global Dynamics and
  3. Atmospheric Chemistry, National Center for Atmospheric Research, 1850 Table Mesa Drive, Boulder, CO 80303;
  4. §Pacific Marine Environmental Laboratory, National Oceanic and Atmospheric Administration, 7600 Sand Point Way NE, Seattle, WA 98115-6349; and
  5. Department of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii at Manoa, 100 Pope Road, Honolulu, HI 96822
  1. Edited by Michael L. Bender, Princeton University, Princeton, NJ, and approved July 9, 2007 (received for review March 9, 2007)

  1. Fig. 1.

    Model-estimated anthropogenic (1990–2000 minus preindustrial) atmospheric deposition fluxes for carbon, nitrogen, and sulfur (mol·m−2·y−1); alkalinity; and potential alkalinity, assuming complete nitrification of NH4 + + NH3 (eq·m−2·y−1).


  2. Fig. 2.

    Perturbations to simulated global vertical profiles due to 10 years of anthropogenic atmospheric nitrogen and sulfur deposition. (Upper) Alkalinity (solid lines) and DIC (dashed lines). (Lower) NO3 (solid lines) and NH4 + (dashed lines). Case 1 is forced with alkalinity flux from Fig. 1, case 2 with the potential alkalinity flux (assuming complete nitrification), and case 3 with alkalinity and nitrogen fluxes allowing for biological feedbacks.


  3. Fig. 3.

    Perturbation maps of simulated surface water pH, DIC, and total alkalinity trends and air–sea CO2 flux due to anthropogenic atmospheric nitrogen and sulfur deposition.


Footnotes

  • To whom correspondence should be addressed. E-mail: sdoney{at}whoi.edu
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