Contribution of isoprene oxidation products to marine aerosol over the north-east atlantic

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 partitio...

Full description

Bibliographic Details
Published in:Advances in Meteorology
Main Authors: Anttila, Tatu, Langmann, Baerbel, Varghese, Saji, O'Dowd, Colin
Format: Article in Journal/Newspaper
Language:unknown
Published: Hindawi Limited 2010
Subjects:
Online Access:http://hdl.handle.net/10379/10264
https://doi.org/10.1155/2010/482603
Description
Summary: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 similar to 5ng 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.