Transport of ozone and pollutants from North America to the North AtlanticOcean during the 1996 Atmosphere/Ocean Chemistry Experiment (AEROCE) intensive
Ai. Prados et al., Transport of ozone and pollutants from North America to the North AtlanticOcean during the 1996 Atmosphere/Ocean Chemistry Experiment (AEROCE) intensive, J GEO RES-A, 104(D21), 1999, pp. 26219-26233
Research flights were conducted to investigate the episodic occurrence of e
nhanced ozone mixing ratios over the North Atlantic Ocean (NAO) during the
spring as part of the Atmosphere/Ocean Chemistry Experiment(AEROCE). We mea
sured meteorological variables, trace gases, and aerosol light scattering f
rom the University of Wyoming King Air research aircraft during 16 research
flights in April and early May 1996. The flights were conducted over easte
rn North America and over the NAO between the United States and Bermuda. On
April 28, a cold front was located just west of Bermuda while a second sys
tem developed over the Midwest and central United States. In the midtroposp
here, polluted layers with up to 250 ppbv CO, 150 pptv NO, and 1.8 ppbv NOy
were observed within a deeper layer of enhanced O-3 mixing ratios (up to 8
8 ppbv) over the NAO at around 32 degrees N, 64-68 degrees W. These aircraf
t observations, when coupled with ozone sondes, back trajectories, and sate
llite image loops, indicate two distinct meteorological mechanisms that com
bine to yield the observed chemical signature of the air. There is substant
ial meteorological evidence, supported by ozone sonde observations and earl
ier King Air flights, indicating that stratosphere/troposphere exchange ass
ociated with the upstream frontal system injects and advects dry, ozone-ric
h air into midtropospheric regions over the continent. These subsiding air
masses have the potential to result in deep layers of enhanced ozone in the
offshore postfrontal area. Convection from the developing (upwind) system
appears to lift air from the continental boundary layer into the area of su
bsidence in the mid to upper troposphere. The result is high concentrations
of gaseous and particulate pollutants along with elevated quantities of oz
one. Ozone mixing ratios exceed those attributable to boundary layer ventin
g or in-transit photochemical production. These meteorological processes le
ad to pollution and enhanced ozone from the stratosphere cooccurring in pos
tfrontal air masses over the NAO.