EGU23-14320, updated on 30 Jun 2023
https://doi.org/10.5194/egusphere-egu23-14320
EGU General Assembly 2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.

Aerosol source identification in the spring and summertime central Arctic Ocean using high-resolution mass spectrometry during MOSAiC.

Benjamin Heutte1, Lubna Dada1,2, Hélène Angot1,4, Imad El Haddad2, Gang Chen2,5, Kaspar R. Dällenbach2, Jakob B. Pernov1, Ivo Beck1, Lauriane Quéléver3, Tiia Laurila3, Tuija Jokinen3,6, and Julia Schmale1
Benjamin Heutte et al.
  • 1Extreme Environments Research Laboratory, Ecole Polytechnique Fédérale de Lausanne, Sion, Switzerland
  • 2Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen, Switzerland
  • 3Insitute for Atmospheric and Earth System Research, INAR/Physics, FI-00014 University of Helsinki, Helsinki, Finland
  • 4CNRS, INRAE, IRD, Grenoble INP, IGE, University Grenoble Alpes, 38000 Grenoble, France
  • 5MRC Centre for Environment and Health, Environmental Research Group, Imperial College London, London, U.K.
  • 6Climate and Atmosphere Research Centre (CARE-C), The Cyprus Institute, 1645 Nicosia, Cyprus

The Arctic region is undergoing considerable changes and is warming at a rate three to four times as fast as the rest of the world. Aerosols, which can originate from natural or anthropogenic sources, both of which can be locally emitted or long-range transported, play a crucial role in the Arctic radiative balance by directly absorbing or scattering incoming solar radiation or indirectly by changing cloud properties and modulating cloud formation mechanisms. Here, we investigate the sources of anthropogenic and natural aerosols in the central Arctic Ocean, using data collected during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition with a high-resolution time-of-flight aerosol mass spectrometer. Using positive matrix factorization on the organic fraction of aerosols during spring and summertime (March – July), we identified six distinct chemical sources of organic aerosols (OA): a hydrocarbon-like factor, a Haze factor, two factors related to two extreme events of warm and moist air mass intrusions (WAMI) in mid-April, an Arctic oxygenated factor, and a Marine factor. We also describe the geographical origin of these factors, inferred from a potential source contribution function applied on 3-hourly back-trajectories. Together, these results suggest that OA from Eurasian anthropogenic origin (including the two extreme WAMI events in mid-April) dominate the central Arctic OA budget until at least the month of May, where episodic spikes in naturally-sourced marine OA, originating from the Fram Strait marginal ice-zone start to become important through June and July. We also highlight a hitherto unreported highly-oxygenated organic factor, whose temporal variability is closely related to that of particulate ammonium (maximum concentration in May) and whose geographical origin, in the Canadian archipelagoes, could indicate a co-emission mechanism of organic aerosols and ammonia from Arctic seabird colonies.

How to cite: Heutte, B., Dada, L., Angot, H., El Haddad, I., Chen, G., Dällenbach, K. R., B. Pernov, J., Beck, I., Quéléver, L., Laurila, T., Jokinen, T., and Schmale, J.: Aerosol source identification in the spring and summertime central Arctic Ocean using high-resolution mass spectrometry during MOSAiC., EGU General Assembly 2023, Vienna, Austria, 23–28 Apr 2023, EGU23-14320, https://doi.org/10.5194/egusphere-egu23-14320, 2023.