HR: 08:25h
AN: A51G-02 [Abstracts]
TI: Uncertainties in Global Aerosol Simulations: Assessment Using Three Meteorological Datasets
AU: * Liu, X
EM: xhliu@engin.umich.edu
AF: University of Michigan, Dept. of Atmos., Oceanic and Space Sciences, 2455 Hayward, Ann Arbor, MI 48109
United States
AU: Penner, J
EM: penner@umich.edu
AF: University of Michigan, Dept. of Atmos., Oceanic and Space Sciences, 2455 Hayward, Ann Arbor, MI 48109
United States
AU: Das, B
EM: bdas@calvin.gsfc.nasa.gov
AF: NASA, Goddard Space Flight Center, Greenbelt, MD 20771
United States
AU: Bergmann, D
EM: dbergmann@llnl.gov
AF: Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, CA 94551
United States
AU: Rodriguez, J
EM: jrodriguez@aurora.gsfc.nasa.gov
AF: NASA, Goddard Space Flight Center, Greenbelt, MD 20771
United States
AU: Strahan, S
EM: strahan@hyperion.gsfc.nasa.gov
AF: NASA, Goddard Space Flight Center, Greenbelt, MD 20771
United States
AU: Wang, M
EM: minghuai@umich.edu
AF: University of Michigan, Dept. of Atmos., Oceanic and Space Sciences, 2455 Hayward, Ann Arbor, MI 48109
United States
AU: Feng, Y
EM: fengy@umich.edu
AF: University of Michigan, Dept. of Atmos., Oceanic and Space Sciences, 2455 Hayward, Ann Arbor, MI 48109
United States
AB:
Current global aerosol models use different physical and chemical schemes and parameters, different meteorological fields,
and often different emission sources. Since the physical and chemical parameterization schemes are often tuned to obtain
results that are consistent with observations, it is difficult to assess the true uncertainty due to meteorology alone. Under
the framework of the NASA global modeling initiative (GMI), the differences and uncertainties in aerosol simulations (for
sulfate, organic carbon, black carbon, dust and sea salt) solely due to different meteorological fields are analyzed and
quantified. Three meteorological datasets available from the NASA DAO GCM, the GISS-II GCM, and the NASA finite volume GCM
(FVGCM) are used to drive the same aerosol model. The global sulfate and mineral dust burdens with FVGCM fields are 40% and
20% less than those with DAO and GISS fields, respectively due to its heavier rainfall. Meanwhile, the sea salt burden
predicted with FVGCM fields is 56% and 43% higher than those with DAO and GISS, respectively, due to its stronger
convection especially over the Southern Hemispheric Ocean. Sulfate concentrations at the surface in the Northern Hemisphere
extratropics and in the middle to upper troposphere differ by more than a factor of 3 between the three meteorological
datasets. The agreement between model calculated and observed aerosol concentrations in the industrial regions (e.g., North
America and Europe) is quite similar for all three meteorological datasets. Away from the source regions, however, the
comparisons with observations differ greatly for DAO, FVGCM and GISS, and the performance of the model using different
datasets varies largely depending on sites and species. Global annual average aerosol optical depth at 550 nm is 0.120-0.131
for the three meteorological datasets. However, the contributions from different aerosol components differ significantly,
which reflects differences in the aerosol spatial distributions. The global annual average anthropogenic and all-sky aerosol
direct forcing at the top-of- the atmosphere is estimated to be -0.75, -0.35, -0.40 W m-2 respectively for DAO, FVGCM, and
GISS fields.
DE: 0305 Aerosols and particles (0345, 4801, 4906)
DE: 0368 Troposphere: constituent transport and chemistry
SC: Atmospheric Sciences [A]
MN: Fall Meeting 2005