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GLOBAL BIOGEOCHEMICAL CYCLES,
VOL. 20,
GB4003,
doi:10.1029/2005GB002672,
2006
Nitrogen and sulfur deposition on regional and global scales: A multimodel evaluation
F. Dentener
European Commission, Institute for Environment and Sustainability, Joint Research Centre, Ispra, Italy
J. Drevet
Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland
J. F. Lamarque
Atmospheric Chemistry Division, National Center of Atmospheric Research, Boulder, Colorado, USA
I. Bey
Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland
B. Eickhout
Netherlands Environmental Assessment Agency (RIVM), Bilthoven, Netherlands
A. M. Fiore
Geophysical Fluid Dynamics Laboratory, NOAA, Princeton, New Jersey, USA
D. Hauglustaine
Laboratoire des Sciences du Climat et de l'Environnement, CEA/CNRS, Gif-sur-Yvette, France
L. W. Horowitz
Geophysical Fluid Dynamics Laboratory, NOAA, Princeton, New Jersey, USA
M. Krol
European Commission, Institute for Environment and Sustainability, Joint Research Centre, Ispra, Italy
U. C. Kulshrestha
Analytical and Environmental Chemistry Division, Indian Institute of Chemical Technology, Hyderabad, India
M. Lawrence
Max Planck Institute for Chemistry, Mainz, Germany
C. Galy-Lacaux
Laboratoire d'Aérologie, Observatoire Midi-Pyrénées, Toulouse, France
S. Rast
Max Planck Institute for Meteorology, Hamburg, Germany
D. Shindell
NASA-Goddard Institute for Space Studies, New York, USA
D. Stevenson
School of Geosciences, Institute for Atmospheric and Environmental Science, University of Edinburgh, UK
T. Van Noije
Atmospheric Composition, Climate Research and Seismology Department, Royal Netherlands Meteorological Institute (KNMI), De
Bilt, Netherlands
C. Atherton
Atmospheric Science Division, Lawrence Livermore National Laboratory, Livermore, California, USA
N. Bell
NASA-Goddard Institute for Space Studies, New York, USA
D. Bergman
Atmospheric Science Division, Lawrence Livermore National Laboratory, Livermore, California, USA
T. Butler
Max Planck Institute for Chemistry, Mainz, Germany
J. Cofala
International Institute for Applied Systems Analysis (IIASA), Laxenburg, Austria
B. Collins
Met Office, Exeter, UK
R. Doherty
School of Geosciences, Institute for Atmospheric and Environmental Science, University of Edinburgh, UK
K. Ellingsen
Department of Geosciences, University of Oslo, Oslo, Norway
J. Galloway
Department of Environmental Sciences, University of Virginia, Charlottesville, Virginia, USA
M. Gauss
Department of Geosciences, University of Oslo, Oslo, Norway
V. Montanaro
Dipartimento di Fisica, Università L'Aquila, Aquila, Italy
J. F. Müller
Belgian Institute for Space Aeronomy, Brussels, Belgium
G. Pitari
Dipartimento di Fisica, Università L'Aquila, Aquila, Italy
J. Rodriguez
Goddard Earth Science and Technology Center (GEST), Baltimore, Maryland, USA
M. Sanderson
Met Office, Exeter, UK
F. Solmon
Laboratoire d'Aérologie, Observatoire Midi-Pyrénées, Toulouse, France
S. Strahan
Goddard Earth Science and Technology Center (GEST), Baltimore, Maryland, USA
M. Schultz
Max Planck Institute for Meteorology, Hamburg, Germany
K. Sudo
Atmospheric Composition Research Program, Frontier Research Center for Global Change (JAMSTEC), Yokohama, Japan
S. Szopa
Laboratoire des Sciences du Climat et de l'Environnement, CEA/CNRS, Gif-sur-Yvette, France
O. Wild
Atmospheric Composition Research Program, Frontier Research Center for Global Change (JAMSTEC), Yokohama, Japan
Abstract
We use 23 atmospheric chemistry transport models to calculate current and future (2030) deposition of reactive nitrogen (NOy, NHx) and sulfate (SOx) to land and ocean surfaces. The models are driven by three emission scenarios: (1) current air quality legislation (CLE);
(2) an optimistic case of the maximum emissions reductions currently technologically feasible (MFR); and (3) the contrasting
pessimistic IPCC SRES A2 scenario. An extensive evaluation of the present-day deposition using nearly all information on wet
deposition available worldwide shows a good agreement with observations in Europe and North America, where 60–70% of the model-calculated
wet deposition rates agree to within ±50% with quality-controlled measurements. Models systematically overestimate NHx deposition in South Asia, and underestimate NOy deposition in East Asia. We show that there are substantial differences among models for the removal mechanisms of NOy, NHx, and SOx, leading to ±1 σ variance in total deposition fluxes of about 30% in the anthropogenic emissions regions, and up to a factor of 2 outside.
In all cases the mean model constructed from the ensemble calculations is among the best when comparing to measurements. Currently,
36–51% of all NOy, NHx, and SOx is deposited over the ocean, and 50–80% of the fraction of deposition on land falls on natural (nonagricultural) vegetation.
Currently, 11% of the world's natural vegetation receives nitrogen deposition in excess of the “critical load” threshold of
1000 mg(N) m−2 yr−1. The regions most affected are the United States (20% of vegetation), western Europe (30%), eastern Europe (80%), South Asia
(60%), East Asia (40%), southeast Asia (30%), and Japan (50%). Future deposition fluxes are mainly driven by changes in emissions,
and less importantly by changes in atmospheric chemistry and climate. The global fraction of vegetation exposed to nitrogen
loads in excess of 1000 mg(N) m−2 yr−1 increases globally to 17% for CLE and 25% for A2. In MFR, the reductions in NOy are offset by further increases for NHx deposition. The regions most affected by exceedingly high nitrogen loads for CLE and A2 are Europe and Asia, but also parts
of Africa.
Received 13
December
2005;
accepted 8
May
2006;
published 28
October
2006.
Keywords: aerosols;
modeling;
nitrogen cycle.
Index Terms: 0469 Biogeosciences: Nitrogen cycling; 0466 Biogeosciences: Modeling; 0545 Computational Geophysics: Modeling (4255).
Read Full Article (file size: 4460347 bytes) Cited by
Citation: Dentener, F., et al.
(2006),
Nitrogen and sulfur deposition on regional and global scales: A multimodel evaluation,
Global Biogeochem. Cycles,
20,
GB4003,
doi:10.1029/2005GB002672.
Copyright 2006 by the American Geophysical Union.
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