Future Inorganic Aerosol Levels 4th GEOS-Chem Users’ Meeting 9 April 2009 Havala Pye* 1 , Hong Liao 2 , Shiliang Wu 3,5 , Loretta Mickley 3 , Daniel Jacob 3 , Daven Henze 4,6 , John Seinfeld 1 1 California Institute of Technology, 2 Chinese Academy of Sciences , 3 Harvard University, 4 Columbia University 5 now at Michigan Technological University 6 now at University of Colorado at Boulder
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Future Inorganic Aerosol Levels 4th GEOS-Chem Users’ Meeting 9 April 2009 Havala Pye* 1, Hong Liao 2, Shiliang Wu 3,5, Loretta Mickley 3, Daniel Jacob.
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Future Inorganic Aerosol Levels
4th GEOS-Chem Users’ Meeting9 April 2009
Future Inorganic Aerosol Levels
4th GEOS-Chem Users’ Meeting9 April 2009
Havala Pye*1, Hong Liao2, Shiliang Wu3,5, Loretta Mickley3, Daniel Jacob3, Daven Henze4,6, John
Seinfeld1
1California Institute of Technology, 2Chinese Academy of Sciences,
3Harvard University, 4Columbia University
5 now at Michigan Technological University6 now at University of Colorado at Boulder
Havala Pye*1, Hong Liao2, Shiliang Wu3,5, Loretta Mickley3, Daniel Jacob3, Daven Henze4,6, John
Seinfeld1
1California Institute of Technology, 2Chinese Academy of Sciences,
3Harvard University, 4Columbia University
5 now at Michigan Technological University6 now at University of Colorado at Boulder
Determine the effect of climate and emissions changes on future sulfate-nitrate-ammonium (SNA) aerosols with a focus on surface concentrations in the U.S.
Objective
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GISS GCM meteorology(year 2000 or 2050)
Anthropogenic emissions(year 2000 or 2050)
GEOS-Chem with ISORROPIA II
sulfatenitrate
ammonium
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Inorganic AerosolsFrom Gas Phase Precursors
DMS gas phase chemistry
SO2 Chemistry
SO42-
Aerosol Phase in Thermodynamic Equilibrium: ISORROPIA II
DMS emission
SO4 emission
SO2 emission
NH4+
water
NH3
NH3 emission
NO3-
HNO3
Na+ Cl-Ca2+
Mg2+K+
NOX chemistry
NOX emission
Sea salt emission
Simulated Present-dayNitrate Concentrations
[µg/m3]
DJF MAM
JJA SON
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Nitrate Predictions Compared to Observations
Sim
ula
ted [
µg/m
3]
Measured [µg/m3]
Sim
ula
ted [
µg/m
3]
Measured [µg/m3]
DJF MAM
JJA SON
• Agreement with observations improved compared to previous ISORROPIA
• Sensitivity tests performed for conditions representative of JJA in So. California
– Predictions not very sensitive to total ammonia available
– Possible model limitation at low RH
Predicted Change in total SNA due to Changes in Climate Alone
(anthropogenic emissions at present-day levels)
Multiple changes potentially important for aerosols including changes in:
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Conclusions
• Climate change alone is predicted to lead to improvements in air quality in the SE U.S. but degraded air quality in the MW and NE– Sulfate increases in the MW and NE– Nitrate generally decreases
• Predicted changes in SNA levels in the U.S. are more strongly influenced by changes in emissions than changes in climate (for the scenario considered here)– SNA levels are generally predicted to be lower due to domestic SO2
emission reductions– Nitrate levels are generally predicted to be higher due to increased NH3
emissions and lower sulfate despite decreasing NOX emissions
• The response of SNA aerosols to climate change depends on the anthropogenic emissions for the MW and NE
For more information see: Pye et al. J. Geophys. Res. 2009
Acknowledgements
This work was supported by the U.S. Environmental Protection Agency’s STAR Program (grants RD830959 and RD833370). Havala Pye was supported by a NSF Graduate Research Fellowship. Hong Liao acknowledges support from the National Natural Science Foundation of China (grant 40775083). Discussions with Becky Alexander and Athanasios Nenes are greatly appreciated.