HR: 1340h
AN: A23A-0771 [Abstracts]
TI: Role of Asian plumes and forest fire smoke on background O3 in the Northeast Pacific/western
U.S.
AU: * Jaffe, D
EM: djaffe@u.washington.edu
AF: University of Washington, 18115 Campus Way NE, Bothell, WA 98011
United States
AU: Weiss-Penzias, P
EM: pweiss@bothell.washington.edu
AF: University of Washington, 18115 Campus Way NE, Bothell, WA 98011
United States
AU: Swartzendruber, P
EM: pswartzendruber@uwb.edu
AF: University of Washington, 18115 Campus Way NE, Bothell, WA 98011
United States
AU: Bertschi, I
EM: isaacpb@u.washington.edu
AF: University of Washington, 18115 Campus Way NE, Bothell, WA 98011
United States
AU: Dennison, J
EM: dennison@u.washington.edu
AF: University of Washington, 18115 Campus Way NE, Bothell, WA 98011
United States
AU: Prestbo, E
EM: ericp@frontiergeosciences.com
AF: Frontier Geosciences, 414 Pontius Ave N, Seattle, WA 98109
United States
AB:
There is some evidence that background ozone in the Northeast Pacific/western U.S. is increasing [Jaffe et al., 2003],
however the exact cause for this increase remains unclear. This is especially true given the multiple sources for
tropospheric O3 in the region. Using ground or airborne datasets the traditional analysis method is to examine the entire
dataset for correlations and relationships. However because of the multiple sources, the correlation of various tracers is
often very weak in the entire dataset and important relationships are masked by atmospheric mixing and chemistry.
An alternate approach is to segregate the dataset into portions with an identifiable influence from an individual source or
group of sources. To do this segregation, we have tried various approaches including trajectories, chemical transport models
and some combination of these with the observations. The enhancement ratios of various species (especially CO to ozone)
then give specific information on the contribution of that source to the regional ozone budget. To investigate the
composition of background O3 and aerosols in the Northeast Pacific/western U.S. our team recently established a new free
tropospheric sampling site on the summit of Mt. Bachelor in central Oregon at 2.7 km above sea level. Because of its
elevation Asian plumes and stratospheric O3 can be more readily identified. In addition, we have also identified
enhancements due to emissions from forest fires in Alaska, Siberia and the western U.S. However even when selecting out one
source type, the ratios still have a large deal of variability, likely reflecting variations in emissions and chemical
processing during transport. For example, during the spring of 2004, we identified numerous episodes of enhanced CO, ozone,
aerosols and elemental mercury associated with sources in Eurasia. During these episodes, we measured enhancement ratios for
ozone to CO and mercury to CO of 0.18 +/- 0.20 ppbv/ppbv and 0.0037 +/- .0031 ng/m3/ppbv (n=10), respectively. By
comparison, plumes from biomass burning emissions have much higher aerosol/CO enhancement ratios and lower Hg/CO ratios.
Based on a comparison of this enhancement ratio with the source ratios, we propose that the Hg/CO ratio is our most specific
indicator of the degree of Asian influence on background air in the western U.S.
DE: 0345 Pollution--urban and regional (0305)
DE: 0365 Troposphere--composition and chemistry
DE: 0368 Troposphere--constituent transport and chemistry
SC: Atmospheric Sciences [A]
MN: 2004 AGU Fall Meeting