Factors controlling atmospheric DMS and its oxidation products (MSA and nssSO42-) in the aerosol at Terra Nova Bay, Antarctica

This paper presents the results on simultaneous high time resolution measurements of biogenic aerosol (methane sulfonic acid-MSA, non-sea salt sulfate nssSO 4 2- ) with its gaseous precursor dimethylsulfide (DMS) performed at the Italian coastal base Mario Zucchelli Station (MZS) in Terra Nova Bay (...

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Main Authors: Becagli, Silvia, Barbaro, Elena, Bonamano, Simone, Caiazzo, Laura, Sarra, Alcide, Feltracco, Matteo, Grigioni, Paolo, Heintzenberg, Jost, Lazzara, Luigi, Legrand, Michel, Madonia, Alice, Marcelli, Marco, Melillo, Chiara, Meloni, Daniela, Nuccio, Caterina, Pace, Giandomenico, Park, Ki-Tae, Preunkert, Suzanne, Severi, Mirko, Vecchiato, Marco, Zangrando, Roberta, Traversi, Rita
Format: Text
Language:English
Published: 2022
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Online Access:https://doi.org/10.5194/acp-2022-195
https://acp.copernicus.org/preprints/acp-2022-195/
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Summary:This paper presents the results on simultaneous high time resolution measurements of biogenic aerosol (methane sulfonic acid-MSA, non-sea salt sulfate nssSO 4 2- ) with its gaseous precursor dimethylsulfide (DMS) performed at the Italian coastal base Mario Zucchelli Station (MZS) in Terra Nova Bay (MZS) during two summer campaigns (2018–2019 and 2019–2020). The study provides information on marine biological activity in the nearby polynya in the Ross Sea and on the influence of biogenic and atmospheric processes on biogenic aerosol formation. Data on atmospheric DMS concentration are scarce especially in Antarctica. The DMS-maximum at MZS occurs in December, one month earlier than at other Antarctic stations. The maximum of DMS concentration is connected with the phytoplanktonic senescent phase following the bloom of Phaeocystis antarctica that occurs in the polynya when sea ice opens up. The second plankton bloom occurs in January and, despite the high Dimethylsulfopropionate (DMSP) concentration in sea water, atmospheric DMS remains low probably due to its fast biological turnover in sea water in this period. The intensity and timing of the DMS evolution during the two years suggests that only the portion of the polynya close to the sampling site produces a discernible effect on the measured DMS. The closeness to the DMS source area, and the occurrence of air masses containing DMS and freshly formed oxidation products allow to study the kinetic of biogenic aerosol formation and the reliable derivation of the branch ratio between MSA and nssSO 4 2- from DMS oxidation that is estimated to be 0.84 ± 0.06. Conversely, for aged airmasses with low DMS content, an enrichment of nssSO 4 2- with respect to MSA, due to the presence of background concentration of nssSO 4 2- from volcanic origin (Erebus) or from long range transport, takes place. Therefore, the aged air mass presents an MSA / nssSO 4 2- ratio lower than in newly formed biogenic aerosol. By considering the sum of MSA and biogenic nssSO 4 2- , we estimate that the mean contribution of biogenic particulate matter to PM 10 is 17 %, with a maximum of 56 %. The high contribution of biogenic aerosol to the total PM 10 mass in summer in this area highlights the dominant role of the polynya on biogenic aerosol formation. Finally, due to the regional and year-to year variability of DMS and related biogenic aerosol formation, we stress the need of long-term measurements of atmospheric DMS and biogenic aerosol along the Antarctic coast and in the Southern Ocean.