Dimethyl sulfide (DMS), sulfur dioxide, non-sea-salt sulfate, and vari
ous aerosol properties were measured during three field programs (two
airborne and one ground-based) near Barrow and Deadhorse (Prudhoe Bay)
, Alaska. The two airborne sampling programs took place in spring and
early summer, and the ground-based measurements spanned an entire summ
er. DMS concentrations in the Arctic atmosphere ranged from a few part
s per trillion by volume (pptv) in spring and fall to higher values in
summer (generally a few tens of pptv with occasional peaks of 100 to
300 pptv). In addition, DMS concentrations were measured during the sp
ring near Resolute in seawater below the ice and in ice-algae and kelp
cultures. The seawater samples taken from below the ice in spring had
DMS concentrations comparable to those in other oceanic regions. Take
n together, these measurements show that the Arctic Ocean is potential
ly a substantial source of DMS, which likely becomes important as sea
ice melts in the early summer. Local atmospheric concentrations increa
sed throughout the summer, peaking in August. In regions where accumul
ation mode aerosols have been scavenged (e.g., by low-level stratus cl
ouds, which are common during the Arctic summer), evidence of rapid ne
w particle production was observed. The seasonal cycle of atmospheric
DMS closely resembles that of fine particles observed at Barrow, Alask
a, and Alert, Northwest Territories, Canada. This finding indicates th
at DMS is likely an important precursor to the types of particles that
dominate the background arctic aerosol in summertime. These results,
together with those from several recently published studies of arctic
aerosol, are combined to yield a consistent picture of the role of loc
ally emitted DMS in the production of atmospheric aerosols in the Arct
ic in summer.