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RESEARCH FRONT

Direct Measurements of New-Particle Fluxes in the Coastal Environment

Robert J. Flanagan A B , Michael Geever A and Colin D. O’Dowd A
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A Department of Experimental Physics and Environmental Change Institute, National University of Ireland, Galway, University Road, Galway, Ireland.

B Corresponding author. Email: robert.flanagan@nuigalway.ie

Environmental Chemistry 2(4) 256-259 https://doi.org/10.1071/EN05069
Submitted: 14 September 2005  Accepted: 12 October 2005   Published: 8 December 2005

Environmental Context. The formation of new secondary aerosol particles in the natural atmosphere is important in terms of controlling the background aerosol population, which significantly impacts on climate. The coastal zone is perhaps the strongest natural source of new secondary aerosol particles, driven by the release of biogenic vapours, which, after undergoing photochemical reactions, lead to the massive production of nucleation mode aerosols, with concentrations often reaching in excess of 106 cm−3. Quantification of this source strength is important, particularly on a regional scale, in terms of estimating the impact of aerosols on climate.

Abstract. Measurements of the flux of new secondary aerosol particles during nucleation events in the coastal environment using an eddy-correlation technique are reported for the first time. Events are divided into two types based on the prevailing wind direction. During tidal-related nucleation events, new-particle upward fluxes are typically of the order of 109–1010 particles m−2 s−1. A close correlation (r2 = 0.86) was found between total particle concentration and total (positive) flux when air masses were not affected by multiple sources. This would suggest that continuous measurements of particle number concentration at Mace Head can be translated into a flux using the resulting parameterization. It is expected that parameterizations obtained from similar data and analysis would be equally feasible at other coastal locations.

Keywords. : aerosol fluxes — aerosol nucleation — climate change — coastal aerosols


Acknowledgments

This work was supported by Enterprise Ireland under contract SC/2001/200, the European Commission under contract EVK-CT-2001-00127 (QUEST) and the Irish Environmental Protection Agency.


References


[1]   C. D. O’Dowd, T. Hoffmann, Environ. Chem. 2005, 2,  245.
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