The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition

Autor: M. Boyer, D. Aliaga, L. L. J. Quéléver, S. Bucci, H. Angot, L. Dada, B. Heutte, L. Beck, M. Duetsch, A. Stohl, I. Beck, T. Laurila, N. Sarnela, R. C. Thakur, B. Miljevic, M. Kulmala, T. Petäjä, M. Sipilä, J. Schmale, T. Jokinen
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Atmospheric Chemistry and Physics, Vol 24, Pp 12595-12621 (2024)
Druh dokumentu: article
ISSN: 1680-7316
1680-7324
DOI: 10.5194/acp-24-12595-2024
Popis: In this study, we present and analyze the first continuous time series of relevant aerosol precursor vapors from the central Arctic (north of 80° N) during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition. These precursor vapors include sulfuric acid (SA), methanesulfonic acid (MSA), and iodic acid (IA). We use FLEXPART simulations, inverse modeling, sulfur dioxide (SO2) mixing ratios, and chlorophyll a (chl a) observations to interpret the seasonal variability in the vapor concentrations and identify dominant sources. Our results show that both natural and anthropogenic sources are relevant for the concentrations of SA in the Arctic, but anthropogenic sources associated with Arctic haze are the most prevalent. MSA concentrations are an order of magnitude higher during polar day than during polar night due to seasonal changes in biological activity. Peak MSA concentrations were observed in May, which corresponds with the timing of the annual peak in chl a concentrations north of 75° N. IA concentrations exhibit two distinct peaks during the year, namely a dominant peak in spring and a secondary peak in autumn, suggesting that seasonal IA concentrations depend on both solar radiation and sea ice conditions. In general, the seasonal cycles of SA, MSA, and IA in the central Arctic Ocean are related to sea ice conditions, and we expect that changes in the Arctic environment will affect the concentrations of these vapors in the future. The magnitude of these changes and the subsequent influence on aerosol processes remains uncertain, highlighting the need for continued observations of these precursor vapors in the Arctic.
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