An Overview of Lagrangian Chemical Measurements During ASTEX/MAGE


B.J. Huebert, A.C. Clarke, L. Zhuang, and J. Porter
Department of Oceanography
University of Hawaii
Honolulu, HI 96822
808-956-6896
huebert@hokulea.soest.hawaii.edu
K.J. Noone, S. Howell, and K.B. Noone
Center for Atmospheric Chemistry Studies
Graduate School of Oceanography
University of Rhode Island
Narragansett, Rl 02882
401-792-6622
A. Bandy, D. Thornton, and B. Blomquist
Department of Chemistry
Drexel University
Philadelphia, PA 19104
215-95 2640
A.BANDY/OMNET
A. Pszenny NOAA/AOML/OCD
4301 Rickenbacker Causeway
Miami, FL 33149-1026
305-361-4388
A.PSZENNY/OMNET

ABSTRACT



During the June, 1992 ASTEX/MAGE experimental program in the Azores we studied the evolution of marine boundary layer chemistry using a Lagrangian strategy. On two occasions we tagged air parcels by launching constant-volume balloons carrying GPS receivers from the R/V Oceanus. Perfluorinated tracers were also released into the tagged air. We then repeatedly sampled in the vicinity of the balloons from aircraft for a period of almost two days, observing the evolution of gas and aerosol chemistry, cloud microphysics, and boundary layer structure with time. The NOAA ship Malcolm Baldrige characterized the air at the end of the trajectories.

We have determined the principal terms in both the total ammonia and non-seasalt sulfate budgets during the two days we followed a polluted European air mass. From the ammonia budget we have estimated the surface emission of ammonia vapor. We have also evaluated the inert tracer data, and have confirmed that some tracer was present in the target air at the end of the two-day trajectory.



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