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JOURNAL OF GEOPHYSICAL RESEARCH,
VOL. 111,
D19306,
doi:10.1029/2006JD007100,
2006
Multimodel simulations of carbon monoxide: Comparison with observations and projected near-future changes
D. T. Shindell
NASA Goddard Institute for Space Studies, Columbia University, New York, New York, USA
G. Faluvegi
NASA Goddard Institute for Space Studies, Columbia University, New York, New York, USA
D. S. Stevenson
School of Geosciences, University of Edinburgh, Edinburgh, UK
M. C. Krol
Space Research Organisation Netherlands, Utrecht, Netherlands
L. K. Emmons
Atmospheric Chemistry Division, National Center for Atmospheric Research, Boulder, Colorado, USA
J.-F. Lamarque
Atmospheric Chemistry Division, National Center for Atmospheric Research, Boulder, Colorado, USA
G. Pétron
Global Monitoring Division, Earth System Research Laboratory, NOAA, Boulder, Colorado, USA
F. J. Dentener
Joint Research Centre, Institute for Environment and Sustainability, European Commission, Ispra, Italy
K. Ellingsen
Department of Geosciences, University of Oslo, Oslo, Norway
M. G. Schultz
Max Planck Institute for Meteorology, Hamburg, Germany
O. Wild
Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, Yokohama, Japan
M. Amann
International Institute for Applied Systems Analysis, Laxenburg, Austria
C. S. Atherton
Atmospheric Science Division, Lawrence Livermore National Laboratory, Livermore, California, USA
D. J. Bergmann
Atmospheric Science Division, Lawrence Livermore National Laboratory, Livermore, California, USA
I. Bey
Ecole Polytechnique Fédéral de Lausanne, Lausanne, Switzerland
T. Butler
Max Planck Institute for Chemistry, Mainz, Germany
J. Cofala
Max Planck Institute for Meteorology, Hamburg, Germany
W. J. Collins
Met Office, Exeter, UK
R. G. Derwent
rdscientific, Newbury, UK
R. M. Doherty
School of Geosciences, University of Edinburgh, Edinburgh, UK
J. Drevet
Ecole Polytechnique Fédéral de Lausanne, Lausanne, Switzerland
H. J. Eskes
Atmospheric Composition Research, Royal Netherlands Meteorological Institute, De Bilt, Netherlands
A. M. Fiore
Geophysical Fluid Dynamics Laboratory, NOAA, Princeton, New Jersey, USA
M. Gauss
Department of Geosciences, University of Oslo, Oslo, Norway
D. A. Hauglustaine
Laboratoire des Sciences du Climat et de l'Environnement, Gif-sur-Yvette, France
L. W. Horowitz
Geophysical Fluid Dynamics Laboratory, NOAA, Princeton, New Jersey, USA
I. S. A. Isaksen
Department of Geosciences, University of Oslo, Oslo, Norway
M. G. Lawrence
Max Planck Institute for Chemistry, Mainz, Germany
V. Montanaro
Dipartimento di Fisica, Università L'Aquila, L'Aquila, Italy
J.-F. Müller
Belgian Institute for Space Aeronomy, Brussels, Belgium
G. Pitari
Dipartimento di Fisica, Università L'Aquila, L'Aquila, Italy
M. J. Prather
Department of Earth System Science, University of California, Irvine, California, USA
J. A. Pyle
Centre for Atmospheric Science, University of Cambridge, Cambridge, UK
S. Rast
Max Planck Institute for Meteorology, Hamburg, Germany
J. M. Rodriguez
Goddard Earth Science and Technology Center, Greenbelt, Maryland, USA
M. G. Sanderson
Max Planck Institute for Chemistry, Mainz, Germany
N. H. Savage
Centre for Atmospheric Science, University of Cambridge, Cambridge, UK
S. E. Strahan
Goddard Earth Science and Technology Center, Greenbelt, Maryland, USA
K. Sudo
Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, Yokohama, Japan
S. Szopa
Laboratoire des Sciences du Climat et de l'Environnement, Gif-sur-Yvette, France
N. Unger
NASA Goddard Institute for Space Studies, Columbia University, New York, New York, USA
T. P. C. van Noije
Atmospheric Composition Research, Royal Netherlands Meteorological Institute, De Bilt, Netherlands
G. Zeng
Centre for Atmospheric Science, University of Cambridge, Cambridge, UK
Abstract
We analyze present-day and future carbon monoxide (CO) simulations in 26 state-of-the-art atmospheric chemistry models run
to study future air quality and climate change. In comparison with near-global satellite observations from the MOPITT instrument
and local surface measurements, the models show large underestimates of Northern Hemisphere (NH) extratropical CO, while typically
performing reasonably well elsewhere. The results suggest that year-round emissions, probably from fossil fuel burning in
east Asia and seasonal biomass burning emissions in south-central Africa, are greatly underestimated in current inventories
such as IIASA and EDGAR3.2. Variability among models is large, likely resulting primarily from intermodel differences in representations
and emissions of nonmethane volatile organic compounds (NMVOCs) and in hydrologic cycles, which affect OH and soluble hydrocarbon
intermediates. Global mean projections of the 2030 CO response to emissions changes are quite robust. Global mean midtropospheric
(500 hPa) CO increases by 12.6 ± 3.5 ppbv (16%) for the high-emissions (A2) scenario, by 1.7 ± 1.8 ppbv (2%) for the midrange
(CLE) scenario, and decreases by 8.1 ± 2.3 ppbv (11%) for the low-emissions (MFR) scenario. Projected 2030 climate changes
decrease global 500 hPa CO by 1.4 ± 1.4 ppbv. Local changes can be much larger. In response to climate change, substantial
effects are seen in the tropics, but intermodel variability is quite large. The regional CO responses to emissions changes
are robust across models, however. These range from decreases of 10–20 ppbv over much of the industrialized NH for the CLE
scenario to CO increases worldwide and year-round under A2, with the largest changes over central Africa (20–30 ppbv), southern
Brazil (20–35 ppbv) and south and east Asia (30–70 ppbv). The trajectory of future emissions thus has the potential to profoundly
affect air quality over most of the world's populated areas.
Received 20
January
2006;
accepted 30
June
2006;
published 14
October
2006.
Keywords: carbon monoxide;
climate change;
emissions.
Index Terms: 0368 Atmospheric Composition and Structure: Troposphere: constituent transport and chemistry; 0322 Atmospheric Composition and Structure: Constituent sources and sinks; 0478 Biogeosciences: Pollution: urban, regional and global (0345, 4251); 1610 Global Change: Atmosphere (0315, 0325).
Read Full Article (file size: 4431963 bytes) Cited by
Citation: Shindell, D. T., et al.
(2006),
Multimodel simulations of carbon monoxide: Comparison with observations and projected near-future changes,
J. Geophys. Res.,
111,
D19306,
doi:10.1029/2006JD007100.
Copyright 2006 by the American Geophysical Union.
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