Monday, 15 January 2001: 1:45 PM
William H. Brune, Penn State University, University Park, PA
The
hydroxyl radical, OH, drives atmospheric oxidation by reacting with chemicals
emitted from Earth's surface, thus creating new chemicals that are more
easily scavenged and removed by aerosols, clouds, and rain. In the oxidation
process, the hydroperoxyl radical, HO
2, is created. Its reaction
with nitric oxide, NO, leads to ozone production. Both atmospheric oxidation
(OH abundance) and ozone production initially increase as NO is added to
the atmosphere, but then decrease as more NO is added. The peak value of
both atmospheric oxidation and ozone production depends not only on NO,
but also on the production rate of the sum of OH and HO
2, called
HO
x.
Recent atmospheric chemistry field studies included measurements of
a large suite of meteorological variables and chemical species, including
the hydroxyl radical, the hydroperoxyl radical, and nitric oxide. The NO
levels and HOx production rates varied widely for the
sampled environments, which include air in remote Pacific Ocean troposphere,
the upper troposphere and lower stratosphere at high latitudes, a moderately
rural forest, and a polluted city. With observations in these diverse environments,
we can examine the fundamental relationships among atmospheric oxidation,
ozone production, NO, and HOx production. This examination involves
both the comparison of observations to photochemical models and the determination
of the functional dependence of the observed OH, HO2, and ozone
production on NOx.
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