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Details

Autor(en) / Beteiligte
Titel
A European aerosol phenomenology – 3: Physical and chemical characteristics of particulate matter from 60 rural, urban, and kerbside sites across Europe
Ist Teil von
  • Atmospheric environment (1994), 2010-03, Vol.44 (10), p.1308-1320
Ort / Verlag
Kidlington: Elsevier Ltd
Erscheinungsjahr
2010
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • This paper synthesizes data on aerosol (particulate matter, PM) physical and chemical characteristics, which were obtained over the past decade in aerosol research and monitoring activities at more than 60 natural background, rural, near-city, urban, and kerbside sites across Europe. The data include simultaneously measured PM 10 and/or PM 2.5 mass on the one hand, and aerosol particle number concentrations or PM chemistry on the other hand. The aerosol data presented in our previous works ( Van Dingenen et al., 2004; Putaud et al., 2004) were updated and merged to those collected in the framework of the EU supported European Cooperation in the field of Scientific and Technical action COST633 ( Particulate matter: Properties related to health effects). A number of conclusions from our previous studies were confirmed. There is no single ratio between PM 2.5 and PM 10 mass concentrations valid for all sites, although fairly constant ratios ranging from 0.5 to 0.9 are observed at most individual sites. There is no general correlation between PM mass and particle number concentrations, although particle number concentrations increase with PM 2.5 levels at most sites. The main constituents of both PM 10 and PM 2.5 are generally organic matter, sulfate and nitrate. Mineral dust can also be a major constituent of PM 10 at kerbside sites and in Southern Europe. There is a clear decreasing gradient in SO 4 2− and NO 3 − contribution to PM 10 when moving from rural to urban to kerbside sites. In contrast, the total carbon/PM 10 ratio increases from rural to kerbside sites. Some new conclusions were also drawn from this work: the ratio between ultrafine particle and total particle number concentration decreases with PM 2.5 concentration at all sites but one, and significant gradients in PM chemistry are observed when moving from Northwestern, to Southern to Central Europe. Compiling an even larger number of data sets would have further increased the significance of our conclusions, but collecting all the aerosol data sets obtained also through research projects remains a tedious task.

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