A092-0009
Long-term Trends for Marine Sulfur Aerosol in the Alaskan Arctic and Relationships with Temperature

Thursday, 10 December 2020
Poster
Claire Elizabeth Elizabeth Moffett1, Tate Edward Barrett2, Jun Liu3, Matthew Gunsch4, Lucia Upchurch5, Patricia Quinn5, Kerri Pratt6 and Rebecca J Sheesley7, (1)Baylor University, Department of Environmental Science, Waco, TX, United States, (2)Baylor University, Department of Geography and the Environment, Denton, TX, United States, (3)Zhejiang University, Hangzhou, China, (4)University of Michigan Ann Arbor, Ann Arbor, MI, United States, (5)Atmospheric Chemistry Group & TPOS 2020 project, University of Washington/JISAO & NOAA/PMEL, Seattle, WA 98115, Seattle, WA, United States, (6)University of Michigan Ann Arbor, Department of Chemistry and Department of Earth & Environmental Sciences, Ann Arbor, MI, United States, (7)Baylor University, Environmental Science, Waco, TX, United States
Abstract:
Marine aerosol can play an important role in cloud-aerosol interactions in the Arctic summer. Increases in temperature and decreases in sea ice extent have the potential to affect marine biogenic aerosol sources. Concentrations in marine sulfur aerosol, such as methanesulfonic acid (MSA) and non-sea-salt sulfate (nss-SO42-), are likely to change as a result. Long term studies of aerosol composition in the Arctic are vital to understand these changes as well as potential interactions with the Arctic climate. Aerosol samples were collected over three summers at two coastal sites on the North Slope of Alaska: Utqiaġvik and Oliktok Point. Results show concentrations of MSA followed previously reported seasonal trends with marine primary productivity influencing both sites. The data was then combined with a data set collected at Utqiaġvik for a 20-year record (1997-2017). Concentrations of MSA had an increase of +2.5% per year, while concentrations of nss-SO42- had an increase of +2.1% per year over the 2 decades. Analysis of meteorological parameters indicates that ambient temperature may be an influence on MSA concentrations, likely related to other factors including sea surface temperature, sea ice extent, and temperature dependent chemical reactions. Analysis of samples at Oliktok Point suggest that having consistent air mass source regions is necessary to observe this relationship with temperature. Individual particle analysis at Oliktok Point also highlight the connection between marine and oil field emissions in the region. The results of this study show how vital continued study and understanding of MSA and other marine sulfur aerosol in the Arctic is.