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Daily PM10 and PM2.5 samples were collected between April 2009 and July 2010 at a rural site (Sinop) situated on the coast of the Central Black Sea. The concentrations of PM10 and PM2.5 were 23.2 +/- 16.7 and 9.8 +/- 6.9 mu g m(-3), respectively. Coarse and fine filters were analyzed for Cl-, NO3 (-), SO4 (2-), C2O4 (2-), PO4 (3-), Na+, NH4 (+), K+, Mg2+, and Ca2+ by using ion chromatography. Elemental and organic carbon content in bulk quartz filters were also analyzed. The highest PM2.5 contribution to PM10 was found in summer with a value of 0.54 due to enhanced secondary aerosols in relation to photochemistry. Cl-, Na+, and Mg2+ illustrated their higher concentrations and variability during winter. Chlorine depletion was chiefly attributed to nitrate. Higher nssCa(2+) concentrations were ascribed to episodic mineral dust intrusions from North Africa into the region. Crustal material (31 %) and sea salt (13 %) were found to be accounted for the majority of the PM10. The ionic mass (IM), particulate organic matter (POM), and elemental carbon (EC) explained 13, 20, and 3 % of the PM10 mass, correspondingly. The IM, POM, and EC dominated the PM2.5 (similar to 74 %) mass. Regarding EU legislation, the exceeded PM2.5 values were found to be associated with secondary aerosols, with a particular dominance of POM. For the exceeded PM10 values, six of the events were dominated by dust while two and four of these exceedances were caused by sea salt and mix events, respectively.

Daily PM10 and PM2.5 samples were collected between April 2009 and July 2010 at a rural site (Sinop) situated on the coast of the Central Black Sea. The concentrations of PM10 and PM2.5 were 23.2 +/- 16.7 and 9.8 +/- 6.9 mu g m(-3), respectively. Coarse and fine filters were analyzed for Cl-, NO3 (-), SO4 (2-), C2O4 (2-), PO4 (3-), Na+, NH4 (+), K+, Mg2+, and Ca2+ by using ion chromatography. Elemental and organic carbon content in bulk quartz filters were also analyzed. The highest PM2.5 contribution to PM10 was found in summer with a value of 0.54 due to enhanced secondary aerosols in relation to photochemistry. Cl-, Na+, and Mg2+ illustrated their higher concentrations and variability during winter. Chlorine depletion was chiefly attributed to nitrate. Higher nssCa(2+) concentrations were ascribed to episodic mineral dust intrusions from North Africa into the region. Crustal material (31 %) and sea salt (13 %) were found to be accounted for the majority of the PM10. The ionic mass (IM), particulate organic matter (POM), and elemental carbon (EC) explained 13, 20, and 3 % of the PM10 mass, correspondingly. The IM, POM, and EC dominated the PM2.5 (similar to 74 %) mass. Regarding EU legislation, the exceeded PM2.5 values were found to be associated with secondary aerosols, with a particular dominance of POM. For the exceeded PM10 values, six of the events were dominated by dust while two and four of these exceedances were caused by sea salt and mix events, respectively.

Although particulate organic and elemental carbon (OC and EC) are important constituents of the suspended atmospheric particulate matter (PM), measurements of OC and EC are much less common and more uncertain than measurements of e.g. the ionic components of PM. In the framework of atmospheric research infrastructures supported by the European Union, actions have been undertaken to determine and mitigate sampling artefacts, and assess the comparability of OC and EC data obtained in a network of 10 atmospheric observatories across Europe. Positive sampling artefacts (from 0.4 to 2.8 μg C/m3) and analytical discrepancies (between −50% and +40% for the EC/TC ratio) have been taken into account to generate a robust data set, from which we established the phenomenology of carbonaceous aerosols at regional background sites in Europe. Across the network, TC and EC annual average concentrations range from 0.4 to 9 μg C/m3, and from 0.1 to 2 μg C/m3, respectively. TC/PM10 annual mean ratios range from 0.11 at a Mediterranean site to 0.34 at the most polluted continental site, and TC/PM2.5 ratios are slightly greater at all sites (0.15–0.42). EC/TC annual mean ratios range from 0.10 to 0.22, and do not depend much on PM concentration levels, especially in winter. Seasonal variations in PM and TC concentrations, and in TC/PM and EC/TC ratios, differ across the network, which can be explained by seasonal changes in PM source contributions at some sites.

International audience ; Although particulate organic and elemental carbon (OC and EC) are important constituents of the suspended atmospheric particulate matter (PM), measurements of OC and EC are much less common and more uncertain than measurements of e.g. the ionic components of PM. In the framework of atmospheric research infrastructures supported by the European Union, actions have been undertaken to determine and mitigate sampling artefacts, and assess the comparability of OC and EC data obtained in a network of 10 atmospheric observatories across Europe. Positive sampling artefacts (from 0.4 to 2.8 μg C/m 3 ) and analytical discrepancies (between -50% and +40% for the EC/TC ratio) have been taken into account to generate a robust data set, from which we established the phenomenology of carbonaceous aerosols at regional background sites in Europe. Across the network, TC and EC annual average concentrations range from 0.4 to 9 μg C/m 3 , and from 0.1 to 2 μg C/m 3 , respectively. TC/PM 10 annual mean ratios range from 0.11 at a Mediterranean site to 0.34 at the most polluted continental site, and TC/PM 2.5 ratios are slightly greater at all sites (0.15-0.42). EC/TC annual mean ratios range from 0.10 to 0.22, and do not depend much on PM concentration levels, especially in winter. Seasonal variations in PM and TC concentrations, and in TC/PM and EC/TC ratios, differ across the network, which can be explained by seasonal changes in PM source contributions at some sites.

International audience ; Although particulate organic and elemental carbon (OC and EC) are important constituents of the suspended atmospheric particulate matter (PM), measurements of OC and EC are much less common and more uncertain than measurements of e.g. the ionic components of PM. In the framework of atmospheric research infrastructures supported by the European Union, actions have been undertaken to determine and mitigate sampling artefacts, and assess the comparability of OC and EC data obtained in a network of 10 atmospheric observatories across Europe. Positive sampling artefacts (from 0.4 to 2.8 μg C/m 3 ) and analytical discrepancies (between -50% and +40% for the EC/TC ratio) have been taken into account to generate a robust data set, from which we established the phenomenology of carbonaceous aerosols at regional background sites in Europe. Across the network, TC and EC annual average concentrations range from 0.4 to 9 μg C/m 3 , and from 0.1 to 2 μg C/m 3 , respectively. TC/PM 10 annual mean ratios range from 0.11 at a Mediterranean site to 0.34 at the most polluted continental site, and TC/PM 2.5 ratios are slightly greater at all sites (0.15-0.42). EC/TC annual mean ratios range from 0.10 to 0.22, and do not depend much on PM concentration levels, especially in winter. Seasonal variations in PM and TC concentrations, and in TC/PM and EC/TC ratios, differ across the network, which can be explained by seasonal changes in PM source contributions at some sites.

Although particulate organic and elemental carbon (OC and EC) are important constituents of the suspended atmospheric particulate matter (PM), measurements of OC and EC are much less common and More uncertain than measurements of e.g. the ionic components of PM. In the framework of atmospheric research infrastructures supported by the European Union, actions have been undertaken to determine and mitigate sampling artefacts, and assess the comparability of OC and EC data obtained in a network of 10 atmospheric observatories across Europe. Positive sampling artefacts (from 0:4 to 2.8 mu g C/m(3)) and analytical discrepancies (between -50% and +40% for the EC/TC ratio) have been taken into account to generate a robust data set, from which we established the phenomenology of carbonaceous aerosols at regional background sites in Europe. Across the network, TC and EC annual average concentrations range from 0.4 to 9 mu g C/m(3), and from 0.1 to 2 mu g C/m(3), respectively. TC/PM10 annual mean ratios range from 0.11 at a Mediterranean site to 0.34 at the most polluted continental site, and TC/PM2.5 ratios are slightly greater at all sites (0.15-0.42). EC/TC annual mean ratios range from 0.10 to 0.22, and do not depend much on PM concentration levels, especially in winter. Seasonal variations in PM and TC concentrations, and in TC/PM and EC/TC ratios, differ across the network, which can be explained by seasonal changes in PM source contributions at some sites. (C) 2016 The Authors. Published by Elsevier Ltd. ; Peer reviewed