Composition and sources of carbonaceous aerosols in Northern Europe during winter
Artikel i vetenskaplig tidskrift, 2018

Sources of elemental carbon (EC) and organic carbon (OC) in atmospheric aerosols (carbonaceous aerosols) were investigated by collection of weekly aerosol filter samples at six background sites in Northern Europe (Birkenes, Norway; Vavihill, Sweden; Risoe, Denmark; Cabauw and Rotterdam in The Netherlands; Melpitz, Germany) during winter 2013. Analysis of 14 C and a set of molecular tracers were used to constrain the sources of EC and OC. During the four-week campaign, most sites (in particular those in Germany and The Netherlands) were affected by an episode during the first two weeks with high concentrations of aerosol, as continental air masses were transported westward. The analysis results showed a clear, increasing north to south gradient for most molecular tracers. Total carbon (TC = OC + EC) at Birkenes showed an average concentration of 0.5 ± 0.3 μg C m −3 , whereas the average concentration at Melpitz was 6.0 ± 4.3 μg C m −3 . One weekly mean TC concentration as high as 11 μg C m −3 was observed at Melpitz. Average levoglucosan concentrations varied by an order of magnitude from 25 ± 13 ng m −3 (Birkenes) to 249 ± 13 ng m −3 (Melpitz), while concentrations of tracers of fungal spores (arabitol and mannitol) and vegetative debris (cellulose) were very low, showing a minor influence of primary biological aerosol particles during the North European winter. The fraction of modern carbon generally varied from 0.57 (Melpitz) to 0.91 (Birkenes), showing an opposite trend compared to the molecular tracers and TC. Total concentrations of 10 biogenic and anthropogenic carboxylic acids, mainly of secondary origin, were 4–53 ng m −3 , with the lowest concentrations observed at Birkenes and the highest at Melpitz. However, the highest relative concentrations of carboxylic acids (normalized to TC) were observed at the most northern sites. Levels of organosulphates and nitrooxy organosulphates varied more than two orders of magnitude, from 2 to 414 ng m −3 , between individual sites and samples. The three sites Melpitz, Rotterdam and Cabauw, located closest to source regions in continental Europe, showed very high levels of organosulphates and nitrooxy organosulphates (up to 414 ng m −3 ) during the first two weeks of the study, while low levels ( < 7 ng m −3 ) were found at all sites except Melpitz during the last week. The large variation in organosulphate levels probably reflects differences in the presence of acidic sulphate aerosols, known from laboratory studies to accelerate the formation of these compounds. On average, the ratio of organic sulphate to inorganic sulphate was 1.5 ± 1.0% (range 0.1–3.4%). Latin-hypercube source apportionment techniques identified biomass burning as the major source of OC for all samples at all sites (typically > 40% of TC), while use and combustion of fossil fuels was the second most important source. Furthermore, EC from biomass burning accounted for 7–16% of TC, whereas EC from fossil sources contributed to < 2–23% of TC, of which the highest percentages were observed for low-concentration aerosol samples. Unresolved non-fossil sources (such as cooking and biogenic secondary organic aerosols) did not account for more than 5–12% of TC. The results confirm that wood combustion is a major source to OC and EC in Northern Europe during winter.

Carboxylic acids



Aerosol sources

Radiocarbon analysis

Source apportionment


M. Glasius

Aarhus Universitet

A. M.K. Hansen

Aarhus Universitet

M. Claeys

Universiteit Antwerpen

J. S. Henzing

Nederlandse Organisatie voor toegepast-natuurwetenschappelijk onderzoek (TNO)

A. D. Jedynska

Nederlandse Organisatie voor toegepast-natuurwetenschappelijk onderzoek (TNO)

A. Kasper-Giebl

Technische Universität Wien

M. Kistler

Technische Universität Wien

K. Kristensen

Aarhus Universitet

J. Martinsson

Lunds universitet

W. Maenhaut

Universiteit Gent

J. K. Nøjgaard

Aarhus Universitet

G. Spindler

Leibniz Institute for Tropospheric Research

K. Stenström

Lunds universitet

E. Swietlicki

Lunds universitet

S. Szidat

Universität Bern

David Simpson

Meteorologisk institutt

Rymd-, geo- och miljövetenskap, Mikrovågs- och optisk fjärranalys, Global miljömätteknik och modellering

K. E. Yttri

Norsk institutt for luftforskning (NILU)

Atmospheric Environment

1352-2310 (ISSN)

Vol. 173 127-141


Meteorologi och atmosfärforskning

Annan geovetenskap och miljövetenskap