New-particle formation, growth and climate-relevant particle production in Egbert, Canada: analysis from 1 year of size-distribution observations
-
Published:2014-08-26
Issue:16
Volume:14
Page:8647-8663
-
ISSN:1680-7324
-
Container-title:Atmospheric Chemistry and Physics
-
language:en
-
Short-container-title:Atmos. Chem. Phys.
Author:
Pierce J. R.ORCID, Westervelt D. M., Atwood S. A., Barnes E. A., Leaitch W. R.
Abstract
Abstract. Aerosol particle nucleation, or new-particle formation, is the dominant contributor to particle number in the atmosphere. However, these particles must grow through condensation of low-volatility vapors without coagulating with the larger, preexisting particles in order to reach climate-relevant sizes (diameters larger than 50–100 nm), where the particles may affect clouds and radiation. In this paper, we use 1 year of size-distribution measurements from Egbert, Ontario, Canada to calculate the frequency of regional-scale new-particle-formation events, new-particle-formation rates, growth rates and the fraction of new particles that survive to reach climate-relevant sizes. Regional-scale new-particle-formation events occur on 14–31% of the days (depending on the stringency of the classification criteria), with event frequency peaking in the spring and fall. New-particle-formation rates and growth rates are similar to those measured at other midlatitude continental sites. We calculate that roughly half of the climate-relevant particles (with diameters larger than 50–100 nm) at Egbert are formed through new-particle-formation events. With the addition of meteorological and SO2 measurements, we find that new-particle formation at Egbert often occurs under synoptic conditions associated with high surface pressure and large-scale subsidence that cause sunny conditions and clean-air flow from the north and west. However, new-particle formation also occurs when air flows from the polluted regions to the south and southwest of Egbert. The new-particle-formation rates tend to be faster during events under the polluted south/southwest flow conditions.
Publisher
Copernicus GmbH
Subject
Atmospheric Science
Reference46 articles.
1. Boy, M., Kulmala, M., Ruuskanen, T. M., Pihlatie, M., Reissell, A., Aalto, P. P., Keronen, P., Dal Maso, M., Hellen, H., Hakola, H., Jansson, R., Hanke, M., and Arnold, F.: Sulphuric acid closure and contribution to nucleation mode particle growth, Atmos. Chem. Phys., 5, 863–878, https://doi.org/10.5194/acp-5-863-2005, 2005. 2. Charlson, R. J., Schwartz, S. E., Hales, J. M., Cess, R. D., Coakley, J. A., Hansen, J. E., and Hofman, D. J.: Climate forcing by anthropogenic aerosols, Science, 255, 423–430, 1992. 3. Crippa, P. and Pryor, S. C.: Spatial and temporal scales of new particle formation events in eastern North America, Atmos. Environ., available from: http://www.sciencedirect.com/science/article/pii/S1352231013003051 75, 257–264, 2013. 4. Croft, B., Pierce, J. R., and Martin, R. V.: Interpreting aerosol lifetimes using the GEOS-Chem model and constraints from radionuclide measurements, Atmos. Chem. Phys. Discuss., 13, 32391–32421, https://doi.org/10.5194/acpd-13-32391-2013, 2013. 5. Dal Maso, M., Kulmala, M., Dal Maso, M., Riipinen, I., Wagner, R., Hussein, T., Aalto, P., and Lehtinen, K. E. J.: Formation and growth of fresh atmospheric aerosols: eight years of aerosol size distribution data from SMEAR II, Hyytiala, Finland, Boreal Env. Res., 10, 323–336, 2005.
Cited by
45 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|