Toward Direct Measurement of Atmospheric Nucleation

Author:

Kulmala Markku12345,Riipinen Ilona12345,Sipilä Mikko12345,Manninen Hanna E.12345,Petäjä Tuukka12345,Junninen Heikki12345,Maso Miikka Dal12345,Mordas Genrik12345,Mirme Aadu12345,Vana Marko12345,Hirsikko Anne12345,Laakso Lauri12345,Harrison Roy M.12345,Hanson Ian12345,Leung Carl12345,Lehtinen Kari E. J.12345,Kerminen Veli-Matti12345

Affiliation:

1. Department of Physical Sciences, University of Helsinki, Post Office Box 64, FI-00014, Helsinki, Finland.

2. Institute of Environmental Physics, University of Tartu, Ülikooli 18, EE-50090, Tartu, Estonia.

3. Division of Environmental Health and Risk Management, School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

4. Department of Physics, University of Kuopio and Finnish Meteorological Institute, Kuopio Unit, Post Office Box 1627, 70211 Kuopio, Finland.

5. Finnish Meteorological Institute, Post Office Box 503, FI-00101, Helsinki, Finland.

Abstract

Atmospheric aerosol formation is known to occur almost all over the world, and the importance of these particles to climate and air quality has been recognized. Although almost all of the processes driving aerosol formation take place below a particle diameter of 3 nanometers, observations cover only larger particles. We introduce an instrumental setup to measure atmospheric concentrations of both neutral and charged nanometer-sized clusters. By applying the instruments in the field, we come to three important conclusions: (i) A pool of numerous neutral clusters in the sub–3 nanometer size range is continuously present; (ii) the processes initiating atmospheric aerosol formation start from particle sizes of ∼1.5 nanometers; and (iii) neutral nucleation dominates over the ion-induced mechanism, at least in boreal forest conditions.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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