Contribution of Isoprene Oxidation Products to Marine Aerosol over the North-East Atlantic
Author(s) -
T. Anttila,
B. Langmann,
Saji Varghese,
Colin O’Dowd
Publication year - 2010
Publication title -
advances in meteorology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.482
H-Index - 32
eISSN - 1687-9317
pISSN - 1687-9309
DOI - 10.1155/2010/482603
Subject(s) - isoprene , aerosol , total organic carbon , environmental science , environmental chemistry , atmospheric sciences , chemistry , meteorology , geography , geology , organic chemistry , copolymer , polymer
Secondary organic aerosol (SOA) formation through isoprene oxidation was investigated with the regional-scale climate model REMOTE. The applied modeling scheme includes a treatment for marine primary organic aerosol emissions, aerosol microphysics, and SOA formation through the gas/particle partitioning of semivolatile, water-soluble oxidation products. The focus was on SOA formation taking place over the North-East Atlantic during a period of high biological activity. Isoprene SOA concentrations were up to ~5 ng m−3 over North Atlantic in the base case model runs, and isoprene oxidation made a negligible contribution to the marine organic aerosol (OA) mass. In particular, isoprene SOA did not account for the observed water-soluble organic carbon (WSOC) concentrations over North Atlantic. The performed model calculations, together with results from recent field measurements, imply a missing source of SOA over remote marine areas unless the isoprene oxidation products are considerably less volatile than the current knowledge indicates
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom