| Literature DB >> 23430652 |
Markku Kulmala1, Jenni Kontkanen, Heikki Junninen, Katrianne Lehtipalo, Hanna E Manninen, Tuomo Nieminen, Tuukka Petäjä, Mikko Sipilä, Siegfried Schobesberger, Pekka Rantala, Alessandro Franchin, Tuija Jokinen, Emma Järvinen, Mikko Äijälä, Juha Kangasluoma, Jani Hakala, Pasi P Aalto, Pauli Paasonen, Jyri Mikkilä, Joonas Vanhanen, Juho Aalto, Hannele Hakola, Ulla Makkonen, Taina Ruuskanen, Roy L Mauldin, Jonathan Duplissy, Hanna Vehkamäki, Jaana Bäck, Aki Kortelainen, Ilona Riipinen, Theo Kurtén, Murray V Johnston, James N Smith, Mikael Ehn, Thomas F Mentel, Kari E J Lehtinen, Ari Laaksonen, Veli-Matti Kerminen, Douglas R Worsnop.
Abstract
Atmospheric nucleation is the dominant source of aerosol particles in the global atmosphere and an important player in aerosol climatic effects. The key steps of this process occur in the sub-2-nanometer (nm) size range, in which direct size-segregated observations have not been possible until very recently. Here, we present detailed observations of atmospheric nanoparticles and clusters down to 1-nm mobility diameter. We identified three separate size regimes below 2-nm diameter that build up a physically, chemically, and dynamically consistent framework on atmospheric nucleation--more specifically, aerosol formation via neutral pathways. Our findings emphasize the important role of organic compounds in atmospheric aerosol formation, subsequent aerosol growth, radiative forcing and associated feedbacks between biogenic emissions, clouds, and climate.Year: 2013 PMID: 23430652 DOI: 10.1126/science.1227385
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728