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Lessons learnt from the first EMEP intensive measurement periods

Authors :
Aas, W.
Tsyro, S.
Bieber, E.
Bergström, Robert
Ceburnis, D.
Ellermann, T.
Fagerli, H.
Froelich, M.
Gehrig, R.
Makkonen, U.
Nemitz, E.
Otjes, R.
Perez, N.
Perrino, C.
Prevot, A. S. H.
Putaud, J. -P
Simpson, D.
Spindler, G.
Vana, M.
Yttri, K. E.
Aas, W.
Tsyro, S.
Bieber, E.
Bergström, Robert
Ceburnis, D.
Ellermann, T.
Fagerli, H.
Froelich, M.
Gehrig, R.
Makkonen, U.
Nemitz, E.
Otjes, R.
Perez, N.
Perrino, C.
Prevot, A. S. H.
Putaud, J. -P
Simpson, D.
Spindler, G.
Vana, M.
Yttri, K. E.
Publication Year :
2012

Abstract

The first EMEP intensive measurement periods were held in June 2006 and January 2007. The measurements aimed to characterize the aerosol chemical compositions, including the gas/aerosol partitioning of inorganic compounds. The measurement program during these periods included daily or hourly measurements of the secondary inorganic components, with additional measurements of elemental- and organic carbon (EC and OC) and mineral dust in PM1, PM2.5 and PM10. These measurements have provided extended knowledge regarding the composition of particulate matter and the temporal and spatial variability of PM, as well as an extended database for the assessment of chemical transport models. This paper summarise the first experiences of making use of measurements from the first EMEP intensive measurement periods along with EMEP model results from the updated model version to characterise aerosol composition. We investigated how the PM chemical composition varies between the summer and the winter month and geographically. The observation and model data are in general agreement regarding the main features of PM10 and PM2.5 composition and the relative contribution of different components, though the EMEP model tends to give slightly lower estimates of PM10 and PM2.5 compared to measurements. The intensive measurement data has identified areas where improvements are needed. Hourly concurrent measurements of gaseous and particulate components for the first time facilitated testing of modelled diurnal variability of the gas/aerosol partitioning of nitrogen species. In general, the modelled diurnal cycles of nitrate and ammonium aerosols are in fair agreement with the measurements, but the diurnal variability of ammonia is not well captured. The largest differences between model and observations of aerosol mass are seen in Italy during winter, which to a large extent may be explained by an underestimation of residential wood burning sources. It should be noted that both primary and s

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1233798935
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.5194.acp-12-8073-2012