Atmospheric nucleation: highlights of the EUCAARI project and future directions

被引:108
作者
Kerminen, V. -M. [1 ,2 ]
Petaja, T. [1 ]
Manninen, H. E. [1 ]
Paasonen, P. [1 ]
Nieminen, T. [1 ]
Sipila, M. [1 ]
Junninen, H. [1 ]
Ehn, M. [1 ]
Gagne, S. [1 ]
Laakso, L. [1 ,12 ]
Riipinen, I. [1 ,13 ]
Vehkamaki, H. [1 ]
Kurten, T. [1 ]
Ortega, I. K. [1 ]
Dal Maso, M. [1 ,6 ]
Brus, D. [2 ]
Hyvarinen, A. [2 ]
Lihavainen, H. [2 ]
Leppa, J. [2 ]
Lehtinen, K. E. J. [2 ,11 ]
Mirme, A. [3 ]
Mirme, S. [3 ]
Horrak, U. [3 ]
Berndt, T. [4 ]
Stratmann, F. [4 ]
Birmili, W. [4 ]
Wiedensohler, A. [4 ]
Metzger, A. [5 ]
Dommen, J. [5 ]
Baltensperger, U. [5 ]
Kiendler-Scharr, A. [6 ]
Mentel, T. F. [6 ]
Wildt, J. [6 ]
Winkler, P. M. [7 ]
Wagner, P. E. [7 ]
Petzold, A. [8 ]
Minikin, A. [8 ]
Plass-Duelmer, C. [9 ]
Poeschl, U. [10 ]
Laaksonen, A. [1 ,11 ]
Kulmala, M. [1 ]
机构
[1] Univ Helsinki, Dept Phys, FIN-00014 Helsinki, Finland
[2] Finnish Meteorol Inst, FIN-00101 Helsinki, Finland
[3] Univ Tartu, Inst Phys, EE-50090 Tartu, Estonia
[4] Leibniz Nstitute Tropospharenforsch, D-04318 Leipzig, Germany
[5] Paul Scherrer Inst, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
[6] Forschungszentrum Julich, Inst Chem & Dynam Geosphare ICG, D-52425 Julich, Germany
[7] Univ Vienna, Fak Phys, A-1090 Vienna, Austria
[8] Inst Phys Atmosphare, Deutsch Zentrum Luft & Raumfarhr, Oberpfaffenhofen, Germany
[9] Hohenpeissenberg Meteorol Observ, Deutsch Wetterdienst, Germany
[10] Max Planck Inst Chem, Biogeochem Dept, D-55128 Mainz, Germany
[11] Univ Eastern Finland, Dept Math & Phys, Kuopio 70211, Finland
[12] North West Univ, Sch Phys & Chem Sci, Potchefstroom, South Africa
[13] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
基金
芬兰科学院;
关键词
ION-INDUCED NUCLEATION; CONDENSATION PARTICLE COUNTERS; CHARGED AEROSOL-PARTICLES; ACID-WATER NUCLEATION; HIGH-ALTITUDE SITE; SULFURIC-ACID; BOREAL FOREST; BOUNDARY-LAYER; GROWTH-RATES; SPECTROMETER MEASUREMENTS;
D O I
10.5194/acp-10-10829-2010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Within the project EUCAARI (European Integrated project on Aerosol Cloud Climate and Air Quality interactions), atmospheric nucleation was studied by (i) developing and testing new air ion and cluster spectrometers, (ii) conducting homogeneous nucleation experiments for sulphate and organic systems in the laboratory, (iii) investigating atmospheric nucleation mechanism under field conditions, and (iv) applying new theoretical and modelling tools for data interpretation and development of parameterisations. The current paper provides a synthesis of the obtained results and identifies the remaining major knowledge gaps related to atmospheric nucleation. The most important technical achievement of the project was the development of new instruments for measuring sub-3 nm particle populations, along with the extensive application of these instruments in both the laboratory and the field. All the results obtained during EUCAARI indicate that sulphuric acid plays a central role in atmospheric nucleation. However, also vapours other than sulphuric acid are needed to explain the nucleation and the subsequent growth processes, at least in continental boundary layers. Candidate vapours in this respect are some organic compounds, ammonia, and especially amines. Both our field and laboratory data demonstrate that the nucleation rate scales to the first or second power of the nucleating vapour concentration(s). This agrees with the few earlier field observations, but is in stark contrast with classical thermodynamic nucleation theories. The average formation rates of 2-nm particles were found to vary by almost two orders of magnitude between the different EUCAARI sites, whereas the formation rates of charged 2-nm particles varied very little between the sites. Overall, our observations are indicative of frequent, yet moderate, ion-induced nucleation usually outweighed by much stronger neutral nucleation events in the continental lower troposphere. The most concrete outcome of the EUCAARI nucleation studies are the new semi-empirical nucleation rate parameterizations based on field observations, along with updated aerosol formation parameterizations.
引用
收藏
页码:10829 / 10848
页数:20
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