Assessment of the water soluble ionic species of suspended particulate matter, collected at a coastal spot, De Haan, Belgium
Horemans, B.; Bencs, L.; Krata, A.; Buczynska, A.J.; Dirtu, A.; Van Meel, K.; Van Grieken, R. (2007). Assessment of the water soluble ionic species of suspended particulate matter, collected at a coastal spot, De Haan, Belgium, in: Mees, J. et al. (Ed.) VLIZ Young Scientists' Day, Brugge, Belgium 2 March 2007: book of abstracts. VLIZ Special Publication, 39: pp. 37 In: Mees, J.; Seys, J. (Ed.) (2007). VLIZ Young Scientists' Day, Brugge, Belgium 2 March 2007: book of abstracts. VLIZ Special Publication, 39. Vlaams Instituut voor de Zee (VLIZ): Oostende. IX, 82 pp., more In: VLIZ Special Publication. Vlaams Instituut voor de Zee (VLIZ): Oostende. ISSN 1377-0950, more | |
Available in | Authors | | Document type: Summary
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Keywords | Analysis > Biochemical analysis Ions Particulates > Suspended particulate matter ANE, Belgium, De Haan [Marine Regions] Marine/Coastal |
Authors | | Top | - Horemans, B.
- Bencs, L.
- Krata, A.
- Buczynska, A.J.
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Abstract | Chemical characterisation of suspended particulate matter (SPM) is very useful for broadening the knowledge concerning processes which are active in the atmosphere (e.g. Lin, 2002). Continental air-masses were found to contain high levels of anthropogenic emitted species, while these levels decreased when the influence changed to an oceanic atmosphere. The high levels of NH4 +, NO3 - and non-sea-salt (NSS) SO4 2- in the fine SPM fraction of continental air-masses (0.38, 0.15μg.N.m-3 and 0.59μg.m-3, respectively) stresses the importance of secondary aerosol formation as a source for SPM. The dominant appearances of Na+, Cl-, Mg2+ and Ca2+ in coarse maritime air masses show the presence of sea-salts and soil dust in the atmosphere at the coastal region. Neutralisation ratios higher than unity (1.20-1.59) for the fine SPM fraction suggested an excess of NH4 +, which was most probably present in the form of NH4Cl due neutralisation of HCl. The latter was formed in atmospheric reactions with sea-salt particles (Kadowaki, 1977), during which HCl escapes (0.13 and 0.58% lost sea-salt chloride for winter and summer, respectively). Correlation analysis showed that warm and dry summer conditions eliminated some influence of sea-salts on atmospheric processes, that where found to be active during winter. NSS SO4 2- was the dominant S-contributor in the fine fraction (83%). During winter, a total SOR value of 0.61 was reached, while summer gave a significant lower value (0.24). These values classified the sampling-site at the Belgian coast as a combined receptor-source area, accepting pollution from the continent and its local surroundings (Shaw and Rodhe, 1982). |
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