1. New insights into aerosol and climate in the Arctic
- Author
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Abbatt, Jonathan P. D., Leaitch, W. Richard, Aliabadi, Amir A., Bertram, Alan K., Blanchet, Jean-Pierre, Boivin-Rioux, Aude, Bozem, Heiko, Burkart, Julia, Chang, Rachel Y. W., Charette, Joannie, Chaubey, Jai P., Christensen, Robert J., Cirisan, Ana, Collins, Douglas B., Croft, Betty, Dionne, Joelle, Evans, Greg J., Fletcher, Christopher G., Ghahremaninezhad, Roghayeh, Girard, Eric, Gong, Wanmin, Gosselin, Michel, Gourdal, Margaux, Hanna, Sarah J., Hayashida, Hakase, Herber, Andreas B., Hesaraki, Sareh, Hoor, Peter, Huang, Lin, Hussherr, Rachel, Irish, Victoria E., Keita, Setigui A., Kodros, John K., Köllner, Franziska, Kolonjari, Felicia, Kunkel, Daniel, Ladino, Luis A., Law, Kathy S., Levasseur, Maurice, Libois, Quentin, Liggio, John, Lizotte, Martine, Macdonald, Katrina M., Mahmood, Rashed, Martin, Randall V., Mason, Ryan H., Miller, Lisa A., Moravek, Alexander, Mortenson, Eric, Mungall, Emma L., Murphy, Jennifer G., Namazi, Maryam, Norman, Ann-Lise, O'Neill, Norman T., Pierce, Jeffrey R., Russell, Lynn M., Schneider, Johannes, Schulz, Hannes, Sharma, Sangeeta, Si, Meng, Staebler, Ralf M., Steiner, Nadja S., Gali, Marti, Thomas, Jennie L., von Salzen, Knut, Wentzell, Jeremy J. B., Willis, Megan D., Wentworth, Gregory R., Xu, Jun-Wei, Yakobi-Hancock, Jacqueline D., Department of Chemistry [University of Toronto], University of Toronto, Environment and Climate Change Canada, School of Engineering [Guelph], University of Guelph, Department of Chemistry [Vancouver] (UBC Chemistry), University of British Columbia (UBC), Département des sciences de la terre et de l'atmosphère [Montréal] (SCTA), Université du Québec à Montréal = University of Québec in Montréal (UQAM), Institut des Sciences de la MER de Rimouski (ISMER), Université du Québec à Rimouski (UQAR), Institute for Atmospheric Physics [Mainz] (IPA), Johannes Gutenberg - Universität Mainz (JGU), Aerosol Physics and Environmental Physics [Vienna], University of Vienna [Vienna], Department of Physics and Atmospheric Science [Halifax], Dalhousie University [Halifax], Department of Chemistry [Lewisburg], Bucknell University, Department of Chemical Engineering and Applied Chemistry (CHEM ENG), Department of Geography and Environmental Management [Waterloo], University of Waterloo [Waterloo], Departement de Biologie [Québec], Université Laval [Québec] (ULaval), School of Earth and Ocean Sciences [Victoria] (SEOS), University of Victoria [Canada] (UVIC), Alfred-Wegener-Institut, Helmholtz-Zentrum für Polar- und Meeresforschung (AWI), Centre d'Applications et de Recherches en TELédétection (CARTEL), Université de Sherbrooke [Sherbrooke], Department of Atmospheric Science [Fort Collins], Colorado State University [Fort Collins] (CSU), Particle Chemistry Department [Mainz], Max Planck Institute for Chemistry (MPIC), Max-Planck-Gesellschaft-Max-Planck-Gesellschaft, Centro de Ciencias de la Atmosfera [Mexico], Universidad Nacional Autónoma de México (UNAM), TROPO - LATMOS, Laboratoire Atmosphères, Milieux, Observations Spatiales (LATMOS), Sorbonne Université (SU)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Sorbonne Université (SU)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS), Department of Biology [Québec], Air Quality Processes Research Section, Canadian Centre for Climate Modelling and Analysis (CCCma), Institute of Ocean Sciences [Sidney] (IOS), Fisheries and Oceans Canada (DFO), Department of Mathematics [Isfahan], University of Isfahan, Department of Physics and Astronomy [Calgary], University of Calgary, Scripps Institution of Oceanography (SIO), University of California [San Diego] (UC San Diego), University of California-University of California, Lawrence Berkeley National Laboratory [Berkeley] (LBNL), and National Research Council of Canada (NRC)
- Subjects
[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph] ,[SDU.STU.CL]Sciences of the Universe [physics]/Earth Sciences/Climatology - Abstract
International audience; Motivated by the need to predict how the Arctic atmosphere will change in a warming world, this article summarizes recent advances made by the research consortium NETCARE (Network on Climate and Aerosols: Addressing Key Uncertainties in Remote Canadian Environments) that contribute to our fundamental understanding of Arctic aerosol particles as they relate to climate forcing. The overall goal of NETCARE research has been to use an interdisciplinary approach encompassing extensive field observations and a range of chemical transport, earth system, and biogeochemical models. Several major findings and advances have emerged from NETCARE since its formation in 2013 . (1) Unexpectedly high summertime dimethyl sulfide (DMS) levels were identified in ocean water and the overlying atmosphere in the Canadian Arctic Archipelago (CAA). Furthermore, melt ponds, which are widely prevalent, were identified as an important DMS source. (2) Evidence was found of widespread particle nucleation and growth in the marine boundary layer in the CAA in the summertime. DMS-oxidation-driven nucleation is facilitated by the presence of atmospheric ammonia arising from sea bird colony emissions, and potentially also from coastal regions, tundra, and biomass burning. Via accumulation of secondary organic material (SOA), a significant fraction of the new particles grow to sizes that are active in cloud droplet formation. Although the gaseous precursors to Arctic marine SOA remain poorly defined, the measured levels of common continental SOA precursors (isoprene and monoterpenes) were low, whereas elevated mixing ratios of oxygenated volatile organic compounds were inferred to arise via processes involving the sea surface microlayer. (3) The variability in the vertical distribution of black carbon (BC) under both springtime Arctic haze and more pristine summertime aerosol conditions was observed. Measured particle size distributions and mixing states were used to constrain, for the first time, calculations of aerosol–climate interactions under Arctic conditions. Aircraft- and ground-based measurements were used to better establish the BC source regions that supply the Arctic via long-range transport mechanisms. (4) Measurements of ice nucleating particles (INPs) in the Arctic indicate that a major source of these particles is mineral dust, likely derived from local sources in the summer and long-range transport in the spring. In addition, INPs are abundant in the sea surface microlayer in the Arctic, and possibly play a role in ice nucleation in the atmosphere when mineral dust concentrations are low. (5) Amongst multiple aerosol components, BC was observed to have the smallest effective deposition velocities to high Arctic snow.
- Published
- 2018