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JOURNAL OF GEOPHYSICAL RESEARCH,
VOL. 108, NO. D2,
8237,
doi:10.1029/2001JD001468,
2003
An assessment of ozone photochemistry in the central/eastern North Pacific as determined from multiyear airborne field studies
B. DiNunno
Department of Earth and Atmospheric Science,
Georgia Institute of Technology,
Atlanta,
Georgia,
USA
D. Davis
Department of Earth and Atmospheric Science,
Georgia Institute of Technology,
Atlanta,
Georgia,
USA
G. Chen
Department of Earth and Atmospheric Science,
Georgia Institute of Technology,
Atlanta,
Georgia,
USA
J. Crawford
NASA Langley Research Center,
Hampton,
Virginia,
USA
J. Olson
NASA Langley Research Center,
Hampton,
Virginia,
USA
S. Liu
Institute of Earth Sciences,
Academica Sinica,
Taipei,
Taiwan
Abstract
In this study, the photochemistry of ozone is examined for the central/eastern North Pacific (CENP), a region bounded by 180°–120°W
and 0°–45°N. Measurements of ozone precursors have been made in this region during 10 previous airborne studies covering the
last two decades. The two seasons for which the most extensive analysis has been possible are spring (March–May) and fall
(September–November). Box model results have been displayed in the form of latitudinal/altitudinal plots for ozone formation,
destruction, and net tendency. They indicate that for both seasons of the year, significant net destruction is found for altitudes
in the 0–4 km range; whereas, at higher altitudes, the ozone tendency calculations lead to small values of net production.
For both seasons, however, the total column integrated ozone trend is one of net destruction. The largest difference between
seasons was in the value for ozone destruction. During springtime, this value was significantly larger than for fall. This
trend coincides with higher average springtime ozone levels. The trends in CENP ozone were also compared to those for the
western Pacific using measurements recorded during PEM-West A (fall 1991) and PEM-West B (spring 1994). While the PEM-West
A results revealed a neutral ozone column tendency, those from PEM-West B showed net production at all altitudes. Both results
are in sharp contrast to those reported here for the CENP region showing net destruction. This suggests that while lightning
and surface emissions of NOx from the northwestern Pacific Rim have a strong influence on the ozone tendency in the surrounding region, due to the combined
effects of dispersion and chemical loss most of this NOx does not reach the CENP region. Hence, ozone in the central Pacific is typically destroyed by photochemistry.
Published 15
January
2003.
Index Terms: 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry; 1610 Global Change: Atmosphere (0315, 0325); 9355 Information Related to Geographic Region: Pacific Ocean.
Read Full Article (file size: 636294 bytes) Cited by
Citation: DiNunno, B., D. Davis, G. Chen, J. Crawford, J. Olson, and S. Liu
(2003),
An assessment of ozone photochemistry in the central/eastern North Pacific as determined from multiyear airborne field studies,
J. Geophys. Res.,
108(D2),
8237,
doi:10.1029/2001JD001468.
Copyright 2003 by the American Geophysical Union.
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