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  Particulate trimethylamine in the summertime Canadian high Arctic lower troposphere

Köllner, F., Schneider, J., Willis, M. D., Klimach, T., Helleis, F., Bozem, H., et al. (2017). Particulate trimethylamine in the summertime Canadian high Arctic lower troposphere. Atmospheric Chemistry and Physics Discussions, 17.

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Köllner, F.1, Autor           
Schneider, J.1, Autor           
Willis, Megan D., Autor
Klimach, T.1, Autor           
Helleis, F.2, Autor           
Bozem, Heiko, Autor
Kunkel, Daniel, Autor
Hoor, Peter, Autor
Burkart, Julia, Autor
Leaitch, W. Richard, Autor
Aliabadi, Amir A., Autor
Abbatt, Jonathan P. D., Autor
Herber, B., Autor
Borrmann, S.1, Autor           
Affiliations:
1Particle Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826291              
2Max Planck Institute for Chemistry, Max Planck Society, ou_1826284              

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 Zusammenfassung: Size-resolved and vertical profile measurements of single particle chemical composition (sampling altitude range 50–3000 m) were conducted in July 2014 in the Canadian high Arctic during the aircraft-based measurement campaign NETCARE 2014. We deployed the single particle laser ablation aerosol mass spectrometer ALABAMA (vacuum aerodynamic diameter range approximately 200–1000 nm) to identify different particle types and their mixing states. On basis of the single particle analysis, we found that a significant fraction (23 %) of all analyzed particles (in total: 7412) contained trimethylamine (TMA). The identification of TMA in ambient mass spectra was confirmed by laboratory measurements. From the maximum occurrence of particulate TMA in the Arctic boundary layer and the higher abundance of smaller TMA-containing particles (maximum in the size distribution at 300 nm), we conclude that the TMA component of these particles resulted from emissions within the Arctic boundary layer. Air mass history according to FLEXPART backward simulations and associated wind data give evidence of a marine-biogenic influence on particulate TMA. The marine influence on particle chemical composition in the summertime Arctic is further demonstrated by the existence of larger sodium and chloride ("Na/Cl-") containing particles which are mainly abundant in the boundary layer. Some of these sea spray particles were internally mixed with carbohydrates (e.g., cellulose) which likely originated from a sea surface microlayer enriched with microorganisms and organic compounds. The external mix of sea spray particles and TMA-containing particles suggests the latter result from secondary conversion of precursor gases from marine inner-Arctic sources. In contrast to TMA- and Na/Cl-containing aerosol types, particles with biomass-burning markers (such as levoglucosan) showed a higher fraction at higher altitudes, thereby indicating long-range transport as their source. Our measurements highlight the importance of natural, marine inner-Arctic sources for summertime Arctic aerosol.

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Sprache(n): eng - English
 Datum: 2017
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.5194/acp-2017-505
 Art des Abschluß: -

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Titel: Atmospheric Chemistry and Physics Discussions
  Kurztitel : Atmos. Chem. Phys. Discuss.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: Katlenburg-Lindau, Germany : European Geophysical Society, Copernicus Publ.
Seiten: 28 Band / Heft: 17 Artikelnummer: - Start- / Endseite: - Identifikator: ISSN: 1680-7367
CoNE: https://pure.mpg.de/cone/journals/resource/111076360006006