The contribution of boundary layer nucleation events to total particle concentrations on regional and global scales

被引:267
作者
Spracklen, D. V.
Carslaw, K. S.
Kulmala, M.
Kerminen, V. -M.
Mann, G. W.
Sihto, S. -L.
机构
[1] Univ Leeds, Sch Earth & Environm, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Helsinki, Dept Phys Sci, FIN-00014 Helsinki, Finland
[3] Finnish Meteorol Inst, FIN-00101 Helsinki, Finland
关键词
D O I
10.5194/acp-6-5631-2006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The contribution of boundary layer (BL) nucleation events to total particle concentrations on the global scale has been studied by including a new particle formation mechanism in a global aerosol microphysics model. The mechanism is based on an analysis of extensive observations of particle formation in the BL at a continental surface site. It assumes that molecular clusters form at a rate proportional to the gaseous sulfuric acid concentration to the power of 1. The formation rate of 3 nm diameter observable particles is controlled by the cluster formation rate and the existing particle surface area, which acts to scavenge condensable gases and clusters during growth. Modelled sulfuric acid vapour concentrations, particle formation rates, growth rates, coagulation loss rates, peak particle concentrations, and the daily timing of events in the global model agree well with observations made during a 22-day period of March 2003 at the SMEAR II station in Hyytiala, Finland. The nucleation bursts produce total particle concentrations (>3 nm diameter) often exceeding 10(4) cm(-3), which are sustained for a period of several hours around local midday. The predicted global distribution of particle formation events broadly agrees with what is expected from available observations. Over relatively clean remote continental locations formation events can sustain mean total particle concentrations up to a factor of 8 greater than those resulting from anthropogenic sources of primary organic and black carbon particles. However, in polluted continental regions anthropogenic primary particles dominate particle number and formation events lead to smaller enhancements of up to a factor of 2. Our results therefore suggest that particle concentrations in remote continental regions are dominated by nucleated particles while concentrations in polluted continental regions are dominated by primary particles. The effect of BL particle formation over tropical regions and the Amazon is negligible. These first global particle formation simulations reveal some interesting sensitivities. We show, for example, that significant reductions in primary particle emissions may lead to an increase in total particle concentration because of the coupling between particle surface area and the rate of new particle formation. This result suggests that changes in emissions may have a complicated effect on global and regional aerosol properties. Overall, our results show that new particle formation is a significant component of the aerosol particle number budget.
引用
收藏
页码:5631 / 5648
页数:18
相关论文
共 79 条
[51]  
Napari I, 2002, J GEOPHYS RES-ATMOS, V107, DOI 10.1029/2002JD002132
[52]  
Nilsson ED, 2001, TELLUS B, V53, P441, DOI 10.1034/j.1600-0889.2001.d01-31.x
[53]   On the photochemical production of new particles in the coastal boundary layer [J].
O'Dowd, C ;
McFiggans, G ;
Creasey, DJ ;
Pirjola, L ;
Hoell, C ;
Smith, MH ;
Allan, BJ ;
Plane, JMC ;
Heard, DE ;
Lee, JD ;
Pilling, MJ ;
Kulmala, M .
GEOPHYSICAL RESEARCH LETTERS, 1999, 26 (12) :1707-1710
[54]   Vertical variability of aerosol properties observed at a continental site during the Lindenberg Aerosol Characterization Experiment (LACE 98) -: art. no. 8128 [J].
Petzold, A ;
Fiebig, M ;
Flentje, H ;
Keil, A ;
Leiterer, U ;
Schröder, F ;
Stifter, A ;
Wendisch, M ;
Wendling, P .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D21)
[55]   Global evaluation of CCN formation by direct emission of sea salt and growth of ultrafine sea salt [J].
Pierce, JR ;
Adams, PJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2006, 111 (D6)
[56]   NUMERICAL ADVECTION BY CONSERVATION OF 2ND-ORDER MOMENTS [J].
PRATHER, MJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1986, 91 (D6) :6671-6681
[57]   A modeling study of size- and chemically resolved aerosol thermodynamics in a global chemical transport model [J].
Rodriguez, MA ;
Dabdub, D .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D2)
[58]   Aerosol states in the free troposphere at northern midlatitudes -: art. no. 8126 [J].
Schröder, F ;
Kärcher, B ;
Fiebig, M ;
Petzold, A .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D21)
[59]   Atmospheric sulphuric acid and aerosol formation:: implications from atmospheric measurements for nucleation and early growth mechanisms [J].
Sihto, S. -L. ;
Kulmala, M. ;
Kerminen, V. -M. ;
Dal Maso, M. ;
Petaja, T. ;
Riipinen, I. ;
Korhonen, H. ;
Arnold, F. ;
Janson, R. ;
Boy, M. ;
Laaksonen, A. ;
Lehtinen, K. E. J. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2006, 6 :4079-4091
[60]   Tethered balloon measurements of biogenic volatile organic compounds at a Boreal forest site [J].
Spirig, C ;
Guenther, A ;
Greenberg, JP ;
Calanca, P ;
Tarvainen, V .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2004, 4 :215-229