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Equal abundance of summertime natural and wintertime anthropogenic Arctic organic aerosols.
Moschos, Vaios; Dzepina, Katja; Bhattu, Deepika; Lamkaddam, Houssni; Casotto, Roberto; Daellenbach, Kaspar R; Canonaco, Francesco; Rai, Pragati; Aas, Wenche; Becagli, Silvia; Calzolai, Giulia; Eleftheriadis, Konstantinos; Moffett, Claire E; Schnelle-Kreis, Jürgen; Severi, Mirko; Sharma, Sangeeta; Skov, Henrik; Vestenius, Mika; Zhang, Wendy; Hakola, Hannele; Hellén, Heidi; Huang, Lin; Jaffrezo, Jean-Luc; Massling, Andreas; Nøjgaard, Jakob K; Petäjä, Tuukka; Popovicheva, Olga; Sheesley, Rebecca J; Traversi, Rita; Yttri, Karl Espen; Schmale, Julia; Prévôt, André S H; Baltensperger, Urs; El Haddad, Imad.
Afiliación
  • Moschos V; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Dzepina K; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Bhattu D; Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany.
  • Lamkaddam H; Center for Atmospheric Research, University of Nova Gorica, Ajdovscina, Slovenia.
  • Casotto R; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Daellenbach KR; Department of Civil and Infrastructure Engineering, Indian Institute of Technology Jodhpur, Jodhpur, India.
  • Canonaco F; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Rai P; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Aas W; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Becagli S; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Calzolai G; Datalystica Ltd, Villigen, Switzerland.
  • Eleftheriadis K; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, Villigen, Switzerland.
  • Moffett CE; Norwegian Institute for Air Research (NILU), Kjeller, Norway.
  • Schnelle-Kreis J; Department of Chemistry 'Ugo Schiff', University of Florence, Florence, Italy.
  • Severi M; Institute of Polar Sciences, ISP-CNR, Venice-Mestre, Italy.
  • Sharma S; National Institute for Nuclear Physics (INFN), Florence Division, Florence, Italy.
  • Skov H; Environmental Radioactivity Laboratory, NCSR Demokritos, Athens, Greece.
  • Vestenius M; Department of Environmental Science, Baylor University, Waco, TX USA.
  • Zhang W; Joint Mass Spectrometry Centre, Helmholtz Zentrum München, München, Germany.
  • Hakola H; Department of Chemistry 'Ugo Schiff', University of Florence, Florence, Italy.
  • Hellén H; Institute of Polar Sciences, ISP-CNR, Venice-Mestre, Italy.
  • Huang L; Climate Research Division, Environment and Climate Change Canada, Toronto, Canada.
  • Jaffrezo JL; Department of Environmental Science, iClimate, Aarhus University, Roskilde, Denmark.
  • Massling A; Atmospheric Composition Research, Finnish Meteorological Institute, Helsinki, Finland.
  • Nøjgaard JK; Climate Research Division, Environment and Climate Change Canada, Toronto, Canada.
  • Petäjä T; Atmospheric Composition Research, Finnish Meteorological Institute, Helsinki, Finland.
  • Popovicheva O; Atmospheric Composition Research, Finnish Meteorological Institute, Helsinki, Finland.
  • Sheesley RJ; Climate Research Division, Environment and Climate Change Canada, Toronto, Canada.
  • Traversi R; Institute of Environmental Geosciences, Université Grenoble Alpes, CNRS, Grenoble, France.
  • Yttri KE; Department of Environmental Science, iClimate, Aarhus University, Roskilde, Denmark.
  • Schmale J; The National Research Centre for the Working Environment, Copenhagen, Denmark.
  • Prévôt ASH; Institute for Atmospheric and Earth System Research/Physics, University of Helsinki, Helsinki, Finland.
  • Baltensperger U; Skobeltsyn Institute of Nuclear Physics, Lomonosov Moscow State University, Moscow, Russia.
  • El Haddad I; Department of Environmental Science, Baylor University, Waco, TX USA.
Nat Geosci ; 15(3): 196-202, 2022.
Article en En | MEDLINE | ID: mdl-35341076
Aerosols play an important yet uncertain role in modulating the radiation balance of the sensitive Arctic atmosphere. Organic aerosol is one of the most abundant, yet least understood, fractions of the Arctic aerosol mass. Here we use data from eight observatories that represent the entire Arctic to reveal the annual cycles in anthropogenic and biogenic sources of organic aerosol. We show that during winter, the organic aerosol in the Arctic is dominated by anthropogenic emissions, mainly from Eurasia, which consist of both direct combustion emissions and long-range transported, aged pollution. In summer, the decreasing anthropogenic pollution is replaced by natural emissions. These include marine secondary, biogenic secondary and primary biological emissions, which have the potential to be important to Arctic climate by modifying the cloud condensation nuclei properties and acting as ice-nucleating particles. Their source strength or atmospheric processing is sensitive to nutrient availability, solar radiation, temperature and snow cover. Our results provide a comprehensive understanding of the current pan-Arctic organic aerosol, which can be used to support modelling efforts that aim to quantify the climate impacts of emissions in this sensitive region.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Geosci Año: 2022 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Geosci Año: 2022 Tipo del documento: Article País de afiliación: Suiza
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