Mass concentrations of total, organic and black carbon were derived by anal
yzing the super-micron and submicron aerosol fractions of shipboard collect
ed samples in the eastern Atlantic Ocean as part of the second Aerosol Char
acterization Experiment (ACE-2). These analyses were complemented by experi
ments intended to estimate the water-soluble fraction of the submicron carb
onaceous material. Our results can be summarized as follows. Depending on t
he sample, between 35% and 80% of total aerosol carbon is associated with t
he submicron fraction. Total submicron carbon was well correlated with blac
k carbon, a unique tracer for incomplete combustion. These correlations and
the approximately constant total to black carbon ratios, suggest that the
majority of submicron total carbon is of primary combustion derived origin.
No systematic relationship between total submicron aerosol carbon and sulf
ate concentrations was found. Sulfate concentrations were, with a few excep
tions, significantly higher than total carbon. Our experiments have demonst
rated that water exposure removed between 36% and 72% of total carbon from
the front filter, suggesting that a substantial fraction of the total submi
cron aerosol organic carbon is water-soluble. An unexpected result of this
study is that water exposure of filter samples caused substantial removal o
f, nominally insoluble, submicron black carbon. Possible reasons for this o
bservation are discussed.