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NOAA Research 2007 Outstanding Scientific Paper Awards
“Large upper tropospheric ozone enhancements above midlatitude
North America during summer: In situ evidence from the IONS and MOZAIC
ozone measurement network”
Owen R. Cooper, Andreas Stohl, Michael Trainer, Anne
M. Thompson, Jacquelyn C. Witte, Samuel J. Oltmans, Gary Morris, Kenneth
E. Pickering, James H. Crawford, Gao Chen, Ronald C. Cohen, Timothy H. Bertram,
Paul J. Wooldridge, Anne E. Perring, William H. Brune, John Merrill, Jennie
L. Moody, David Tarasick, Philippe Nédélec, Gerry Forbes, Michael
J. Newchurch, Frank J. Schmidlin, Bryan J. Johnson Solene Turquety, Steven
L. Baughcum, Xinrong Ren, Fred. C. Fehsenfeld, James F. Meagher, Nicole Spichtinger,
Clyde C. Brown, Stuart A. McKeen, I. Stuart McDermid, and Thierry Leblanc
ABSTRACT
The most extensive set of free tropospheric ozone measurements ever compiled
across midlatitude North America was measured with daily ozonesondes, commercial
aircraft and a lidar at 14 sites during July-August 2004. The model estimated
stratospheric ozone was subtracted from all profiles, leaving a tropospheric
residual ozone. On average the upper troposphere above midlatitude eastern
North America contained 15 ppbv more tropospheric residual ozone than the
more polluted layer between the surface and 2 km above sea level. Lowest
ozone values in the upper troposphere were found above the two upwind sites
in California. The upper troposphere above midlatitude eastern North America
contained 16 ppbv more tropospheric residual ozone than the upper troposphere
above three upwind sites, with the greatest enhancement above Houston,
Texas, at 24 ppbv. Upper tropospheric CO measurements above east Texas
show no statistically significant enhancement compared to west coast measurements,
arguing against a strong influence from fresh surface anthropogenic emissions
to the upper troposphere above Texas where the ozone enhancement is greatest.
Vertical mixing of ozone from the boundary layer to the upper troposphere
can only account for 2 ppbv of the 16 ppbv ozone enhancement above eastern
North America; therefore the remaining 14 ppbv must be the result of in
situ ozone production. The transport of NOx tracers from North
American anthropogenic, biogenic, biomass burning, and lightning emissions
was simulated for the upper troposphere of North America with a particle
dispersion model. Additional box model calculations suggest the 24 ppbv
ozone enhancement above Houston can be produced over a 10 day period from
oxidation reactions of lightning NOx and background mixing ratios
of CO and CH4. Overall, we estimate that 69–84% (11–13
ppbv) of the 16 ppbv ozone enhancement above eastern North America is due
to in situ ozone production from lightning NOx with the remainder
due to transport of ozone from the surface or in situ ozone production
from other sources of NOx. FULL
TEXT
Cumulative
lightning N emissions from CG and IC flashes between 21 June and 15 August
2004. (larger image)
Locations of the fourteen ozone profile sites in 2004:
T, Trinidad Head; L, Table Mountain/MOZAIC; H, Houston; V, Huntsville;
A, Atlanta; W, Wallops Island; D, Washington DC; Y, New York City; N, Narragansett;
B, research vessel Ronald H. Brown; S, Sable Island; M, Montreal; O, Ontario;
and P, Pellston. The locations of the tropical portions of the MOZAIC flights
to and from Caracas (C) during 1999–2004 are also shown. (larger
image)
Distributions of measured NOx (blue) from the
DC8 above eastern North America during 1 July to 15 August 2004 and the
corresponding FLEXPART lightning NOx tracer values (red). Shown
are the median values (solid lines) and the 10th and 90th percentiles (dashed
lines) with modeled NOx lifetimes of (a) 1 day, (b) 2 days,
and (c) 4 days. (larger image)
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10/22/07