M. Posfai et al., COMPOSITIONAL VARIATIONS OF SEA-SALT-MODE AEROSOL-PARTICLES FROM THE NORTH-ATLANTIC, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 100(D11), 1995, pp. 23063-23074
Individual sea-salt-mode aerosol particles collected during the Atlant
ic Stratocumulus Transition Experiment/Marine Aerosol and Gas Exchange
(ASTEX/MAGE) experiment in June 1992 were studied using transmission
electron microscopy in both imaging and analysis modes. The set of eig
ht samples provided an opportunity to compare ''clean,'' ''intermediat
e,'' and ''dirty'' oceanic aerosols. In the clean samples, major speci
es include NaCl, mixed-cation (Na, Mg, K, and Ca) sulfates, and in som
e particles, NaNO3. The same compounds also occur in intermediate samp
les, but compositional groups can be distinguished that are characteri
zed by low- and high-Cl losses from sea salt. In these samples, most C
l loss is compensated by NaNO3 formation. Several compositional groups
occur in the dirty samples; these include, in addition to the particl
e types in clean and intermediate samples, Na2SO4 (with minor Mg, K, a
nd Ca), (NH4)(2)SO4, and silicates. The uniform compositions of sea-sa
lt-mode particles in the clean samples suggest that the same process w
as acting on all particles. Their excess sulfate and nitrate probably
formed through the oxidation of SO2 in the sea-salt aerosol water and
by reactions between NOx and NaCl. On the other hand, distinct composi
tional groups in the dirty samples reveal that long-range transport of
continental air masses resulted in the mixing of aerosols that were e
xposed to different conditions. In addition to O-3 oxidation, cloud pr
ocessing may have contributed to the formation of excess sulfate in th
ese samples.