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      Direct Observations of Atmospheric Aerosol Nucleation

      1 , 1 , 1 , 1 , 1 , 1 , 2 , 1 , 1 , 1 , 1 , 1 , 1 ,   1 , 1 , 1 , 1 , 1 , 1 , 3 , 3 , 4 , 5 , 5 , 1 , 1 , 6 , 1 , 1 , 7 , 8 , 9 , 1 , 10 , 11 , 8 , 12 , 1 , 13 , 13 , 5 , 8 , 5 , 8 , 1 , 1 , 5 , 8 , 14
      Science
      American Association for the Advancement of Science (AAAS)

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          Aerosol Formation

          Most atmospheric aerosol particles result from a growth process that begins with atmospheric molecules and clusters, progressing to larger and larger sizes as they acquire other molecules, clusters, and particles. The initial steps of this process involve very small entities—with diameters of less than 2 nanometers—which have been difficult to observe. Kulmala et al. (p. [Related article:]943 ; see the Perspective by [Related article:]Andreae ) developed a sensitive observational protocol that allows these tiny seeds to be detected and counted, and they mapped out the process of aerosol formation in detail.

          Abstract

          Detailed aerosol measurements provide a consistent framework for the formation of particles from atmospheric gases. [Also see Perspective by [Related article:]Andreae ]

          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.

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          Most cited references63

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          Nucleation and growth of nanoparticles in the atmosphere.

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            Impact of nucleation on global CCN

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              The Role of Sulfuric Acid in Atmospheric Nucleation

              Nucleation is a fundamental step in atmospheric new-particle formation. However, laboratory experiments on nucleation have systematically failed to demonstrate sulfuric acid particle formation rates as high as those necessary to account for ambient atmospheric concentrations, and the role of sulfuric acid in atmospheric nucleation has remained a mystery. Here, we report measurements of new particles (with diameters of approximately 1.5 nanometers) observed immediately after their formation at atmospherically relevant sulfuric acid concentrations. Furthermore, we show that correlations between measured nucleation rates and sulfuric acid concentrations suggest that freshly formed particles contain one to two sulfuric acid molecules, a number consistent with assumptions that are based on atmospheric observations. Incorporation of these findings into global models should improve the understanding of the impact of secondary particle formation on climate.
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                Author and article information

                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                February 22 2013
                February 22 2013
                : 339
                : 6122
                : 943-946
                Affiliations
                [1 ]Department of Physics, University of Helsinki, Finland.
                [2 ]Helsinki Institute of Physics, Helsinki, Finland.
                [3 ]Airmodus Oy, Helsinki, Finland.
                [4 ]SMEAR Station II, Hyytiälä, Finland.
                [5 ]Finnish Meteorological Institute, Finland.
                [6 ]University of Colorado at Boulder, Boulder, CO, USA.
                [7 ]Department of Forest Sciences, University of Helsinki, Finland.
                [8 ]University of Eastern Finland, Kuopio, Finland.
                [9 ]University of Stockholm, Stockholm, Sweden.
                [10 ]Department of Chemistry, University of Helsinki, Finland.
                [11 ]University of Delaware, Newark, DE, USA.
                [12 ]National Center for Atmospheric Research, Boulder, CO, USA.
                [13 ]Forschungszentrum Juelich, IEK-8, 52425 Juelich, Germany.
                [14 ]Aerodyne Research, Billerica, MA, USA.
                Article
                10.1126/science.1227385
                23430652
                ac99b683-6567-4a11-adad-d9fd4370748a
                © 2013
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