Atmos. Chem. Phys. Discuss., 8, 7805-7846, 2008
www.atmos-chem-phys-discuss.net/8/7805/2008/
doi:10.5194/acpd-8-7805-2008
© Author(s) 2008. This work is distributed
under the Creative Commons Attribution 3.0 License.
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This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Sources of organic carbon in PM1 in Helsinki urban air
S. Saarikoski1, H. Timonen1, K. Saarnio1, M. Aurela1, L. Järvi2, P. Keronen2, V.-M. Kerminen1, and R. Hillamo1
1Finnish Meteorological Institute, Air Quality, P.O. Box 503, 00101 Helsinki, Finland
2University of Helsinki, Department of Physics, P.O. Box 64, 00014 Helsinki, Finland

Abstract. A major fraction of fine particle matter consists of organic carbon (OC) but its origin is still inadequately known. In this study the sources of OC were investigated in the northern European urban environment in Helsinki, Finland. Measurements were carried out over one year and they included both filter (PM1) and online methods. From the filter samples OC, elemental carbon (EC), water-soluble OC (WSOC), levoglucosan and major ions were analyzed. Filter data together with the concentrations of inorganic gases were analyzed by Positive matrix factorization (PMF) method in order to find the sources of OC (and WSOC) on an annual as well as on a seasonal basis. In order to study the diurnal variation of sources, OC and EC were measured by a semicontinuous OC/EC analyzer and major ions were determined by a Particle-into-Liquid Sampler coupled to ion chromatographs. According to PMF, OC concentrations were impacted by four sources: biomass combustion, traffic, long-range transport and secondary production. On an annual basis the OC concentration was dominated by secondary organic aerosol (SOA). Its contribution to OC was as high as 64% in summer, which may result besides anthropogenic sources also from the large biogenic VOC emissions in the boreal region. In winter biomass combustion constituted the largest fraction in OC due to domestic wood combustion for heating purposes. Traffic contributed to OC from 15 to 27%. Regarding the diurnal variation, the contribution of traffic was higher from 08:00 to 18:00 on weekdays than on weekends. The contribution of long-range transport to OC was 24% on average. All four sources influenced also on the WSOC concentrations, however, the contribution of SOA was significantly larger to WSOC than to OC.

Citation: Saarikoski, S., Timonen, H., Saarnio, K., Aurela, M., Järvi, L., Keronen, P., Kerminen, V.-M., and Hillamo, R.: Sources of organic carbon in PM1 in Helsinki urban air, Atmos. Chem. Phys. Discuss., 8, 7805-7846, doi:10.5194/acpd-8-7805-2008, 2008.
 
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