Atmospheric sub-3 nm particles at high altitudes

被引:68
作者
Mirme, S. [1 ]
Mirme, A. [1 ]
Minikin, A. [2 ]
Petzold, A. [2 ]
Horrak, U. [1 ]
Kerminen, V. -M. [3 ]
Kulmala, M. [4 ]
机构
[1] Univ Tartu, Inst Phys, EE-50090 Tartu, Estonia
[2] Inst Phys Atmosphare, Deutsch Zentrum Luft & Raumfahrt DLR, Oberpfaffenhofen, Germany
[3] Finnish Meteorol Inst, FIN-00101 Helsinki, Finland
[4] Univ Helsinki, Dept Phys, Helsinki 00014, Finland
基金
芬兰科学院;
关键词
CLOUD CONDENSATION NUCLEI; AIR ION SPECTROMETER; AIRBORNE MEASUREMENTS; GROWTH-RATES; TROPOSPHERIC AEROSOLS; NUCLEATION EVENTS; SIZE; NANOPARTICLES; COUNTERS; CLUSTERS;
D O I
10.5194/acp-10-437-2010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Formation of new atmospheric aerosol particles is known to occur almost all over the world and the importance of these particles to climate and air quality has been recognized. Recently, it was found that atmospheric aerosol particle formation begins at the diameter of around 1.5-2.0 nm and a pool of sub-3 nm atmospheric particles - consisting of both charged and uncharged ones - was observed at the ground level. Here, we report on the first airborne observations of the pool of sub-3 nm neutral atmospheric particles. Between 2 and 3 nm, their concentration is roughly two orders of magnitude larger than that of the ion clusters, depending slightly on the altitude. Our findings indicate that new particle formation takes place throughout the tropospheric column up to the tropopause. Particles were found to be formed via neutral pathways in the boundary layer, and there was no sign of an increasing role by ion-induced nucleation toward the upper troposphere. Clouds, while acting as a source of sub-10 nm ions, did not perturb the overall budget of atmospheric clusters or particles.
引用
收藏
页码:437 / 451
页数:15
相关论文
共 50 条
[1]   Atmospheric aerosol and cloud condensation nuclei formation: A possible influence of cosmic rays? [J].
Arnold, F. .
SPACE SCIENCE REVIEWS, 2006, 125 (1-4) :169-186
[2]   Results of the first air ion spectrometer calibration and intercomparison workshop [J].
Asmi, E. ;
Sipila, M. ;
Manninen, H. E. ;
Vanhanen, J. ;
Lehtipalo, K. ;
Gagne, S. ;
Neitola, K. ;
Mirme, A. ;
Mirme, S. ;
Tamm, E. ;
Uin, J. ;
Komsaare, K. ;
Attoui, M. ;
Kulmala, M. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (01) :141-154
[3]   Small-scale cloud processes and climate [J].
Baker, Marcia B. ;
Peter, Thomas .
NATURE, 2008, 451 (7176) :299-300
[4]   The effects of airmass history on new particle formation in the free troposphere: case studies [J].
Benson, D. R. ;
Young, Li-Hao ;
Lee, Shan-Hu ;
Campos, T. L. ;
Rogers, D. C. ;
Jensen, J. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2008, 8 (12) :3015-3024
[5]   PARTICLE FORMATION IN THE UPPER TROPICAL TROPOSPHERE - A SOURCE OF NUCLEI FOR THE STRATOSPHERIC AEROSOL [J].
BROCK, CA ;
HAMILL, P ;
WILSON, JC ;
JONSSON, HH ;
CHAN, KR .
SCIENCE, 1995, 270 (5242) :1650-1653
[7]   Aerosol production and growth in the upper free troposphere [J].
de Reus, M ;
Ström, J ;
Curtius, J ;
Pirjola, L ;
Vignati, E ;
Arnold, F ;
Hansson, HC ;
Kulmala, M ;
Lelieveld, J ;
Raes, F .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2000, 105 (D20) :24751-24762
[8]   Do organics contribute to small particle formation in the Amazonian upper troposphere? [J].
Ekman, Annica M. L. ;
Krejci, Radovan ;
Engstrom, Anders ;
Strom, Johan ;
de Reus, Marian ;
Williams, Jonathan ;
Andreae, Meinrat O. .
GEOPHYSICAL RESEARCH LETTERS, 2008, 35 (17)
[9]  
Fuchs N.A., 1964, MECH AEROSOLS, DOI DOI 10.1002/QJ.49709138822
[10]  
FUCHS NA, 1971, TOPICS CURRENT AEROS, VH