Frequent ultrafine particle formation and growth in Canadian Arctic marine and coastal environments

• Published in: Atmospheric Chemistry and Physics
• Main Authors: D. B. Collins, J. Burkart, R. Y.-W. Chang, M. Lizotte, A. Boivin-Rioux, M. Blais, E. L. Mungall, M. Boyer, V. E. Irish, G. Massé, D. Kunkel, J.-É. Tremblay, T. Papakyriakou, A. K. Bertram, H. Bozem, M. Gosselin, M. Levasseur, J. P. D. Abbatt
• Format: Article in Journal/Newspaper
• Language: English
• Published: Copernicus Publications 2017
• Subjects: Physics; QC1-999; Chemistry; QD1-999; Arctic; Sea ice
• Online Access: https://doi.org/10.5194/acp-17-13119-2017; https://doaj.org/article/b26ec1a3d51b49c08d0ccd11948b7110

The source strength and capability of aerosol particles in the Arctic to act as cloud condensation nuclei have important implications for understanding the indirect aerosol–cloud effect within the polar climate system. It has been shown in several Arctic regions that ultrafine particle (UFP) formation and growth is a key contributor to aerosol number concentrations during the summer. This study uses aerosol number size distribution measurements from shipboard expeditions aboard the research icebreaker CCGS Amundsen in the summers of 2014 and 2016 throughout the Canadian Arctic to gain a deeper understanding of the drivers of UFP formation and growth within this marine boundary layer. UFP number concentrations (diameter > 4 nm) in the range of 10 1 –10 4 cm −3 were observed during the two seasons, with concentrations greater than 10 3 cm −3 occurring more frequently in 2016. Higher concentrations in 2016 were associated with UFP formation and growth, with events occurring on 41 % of days, while events were only observed on 6 % of days in 2014. Assessment of relevant parameters for aerosol nucleation showed that the median condensation sink in this region was approximately 1.2 h −1 in 2016 and 2.2 h −1 in 2014, which lie at the lower end of ranges observed at even the most remote stations reported in the literature. Apparent growth rates of all observed events in both expeditions averaged 4.3 ± 4.1 nm h −1 , in general agreement with other recent studies at similar latitudes. Higher solar radiation, lower cloud fractions, and lower sea ice concentrations combined with differences in the developmental stage and activity of marine microbial communities within the Canadian Arctic were documented and help explain differences between the aerosol measurements made during the 2014 and 2016 expeditions. These findings help to motivate further studies of biosphere–atmosphere interactions within the Arctic marine environment to explain the production of UFP and their growth to sizes relevant for cloud droplet activation.