Ds. Covert et al., AEROSOL NUMBER SIZE DISTRIBUTIONS FROM 3 TO 500 NM DIAMETER IN THE ARCTIC MARINE BOUNDARY-LAYER DURING SUMMER AND AUTUMN, Tellus. Series B, Chemical and physical meteorology, 48(2), 1996, pp. 197-212
Aerosol physics measurements made onboard the Swedish icebreaker Oden
in the late Summer and early Autumn of 1991 during the International A
rctic Ocean Expedition (IAOE-91) have provided the first data on the s
ize distribution of particles in the Arctic marine boundary layer (MEL
) that cover both the number and mass modes of the size range from 3 t
o 500 nm diameter. These measurements were made in conjunction with at
mospheric gas and condensed phase chemistry measurements in an effort
to understand a part of the ocean-atmosphere sulfur cycle. Analysis of
the particle physics data showed that there were three distinct numbe
r modes in the submicrometric aerosol in the Arctic MEL. These modes h
ad geometric mean diameters of around 170 nm, 45 nm and 14 nm referred
to as accumulation, Aitken and ultrafine modes, respectively. There w
ere clear minima in number concentrations between the modes that appea
red at 20 to 30 nm and at 80 to 100 nm. The total number concentration
was most frequently between 30 and 60 particles cm(-3) with a mean va
lue of around 100 particles cm(-3), but the hourly average concentrati
on varied over two to three orders of magnitude during the 70 days of
the expedition. On average, the highest concentration was in the accum
ulation mode that contained about 45% of the total number, while the A
itken mode contained about 40%. The greatest variability was in the ul
trafine mode concentration which is indicative of active, nearby sourc
es (nucleation from the gas phase) and sinks; the Aitken and accumulat
ion mode concentrations were much less variable. The ultrafine mode wa
s observed about two thirds of the time and was dominant 10% of the ti
me. A detailed description and statistical analysis of the modal aeros
ol parameters is presented here.