MALTE - model to predict new aerosol formation in the lower troposphere

被引:51
作者
Boy, M.
Hellmuth, O.
Korhonen, H.
Nilsson, E. D.
ReVelle, D.
Turnipseed, A.
Arnold, F.
Kulmala, M.
机构
[1] Univ Helsinki, Dept Phys Sci, Div Atmospher Sci, FIN-00014 Helsinki, Finland
[2] NCAR, ASP ACD, Boulder, CO 80305 USA
[3] Leibniz Inst Tropospher Res, D-04318 Leipzig, Germany
[4] Finnish Meteorol Inst, Helsinki 00880, Finland
[5] Univ Stockholm, Dept Meteorol, S-10691 Stockholm, Sweden
[6] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[7] NCAR, ACD, Boulder, CO 80305 USA
[8] Max Planck Inst Nucl Phys, Atmospher Phys Div, D-69029 Heidelberg, Germany
关键词
D O I
10.5194/acp-6-4499-2006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The manuscript presents a detailed description of the meteorological and chemical code of Malte - a model to predict new aerosol formation in the lower troposphere. The aerosol dynamics are achieved by the new developed UHMA (University of Helsinki Multicomponent Aerosol Model) code with kinetic limited nucleation as responsible mechanism to form new clusters. First results indicate that the model is able to predict the on- and offset of new particle formation as well as the total aerosol number concentrations that were in good agreement with the observations. Further, comparison of predicted and measured H2SO4 concentrations showed a satisfactory agreement. The simulation results indicated that at a certain transitional particle diameter (2-7 nm), organic molecules can begin to contribute significantly to the growth rate compared to sulphuric acid. At even larger particle sizes, organic molecules can dominate the growth rate on days with significant monoterpene concentrations. The intraday vertical evolution of newly formed clusters and particles in two different size ranges resulted in two maxima at the ground. These particles grow around noon to the detectable size range and agree well with measured vertical profiles.
引用
收藏
页码:4499 / 4517
页数:19
相关论文
共 59 条
[51]   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
[52]   LONG-PERIOD MODELING OF PHOTOCHEMICAL OXIDANTS IN EUROPE - MODEL-CALCULATIONS FOR JULY 1985 [J].
SIMPSON, D .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1992, 26 (09) :1609-1634
[53]   New-particle formation events in a continental boundary layer: first results from the SATURN experiment [J].
Stratmann, F ;
Siebert, H ;
Spindler, G ;
Wehner, B ;
Althausen, D ;
Heintzenberg, J ;
Hellmuth, O ;
Rinke, R ;
Schmieder, U ;
Seidel, C ;
Tuch, T ;
Uhrner, U ;
Wiedensohler, A ;
Wandinger, U ;
Wendisch, M ;
Schell, D ;
Stohl, A .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2003, 3 :1445-1459
[54]  
Stull RB, 1997, INTRO BOUNDARY LAYER
[55]   LONG-WAVE RADIATION FROM CLEAR SKIES [J].
SWINBANK, WC .
QUARTERLY JOURNAL OF THE ROYAL METEOROLOGICAL SOCIETY, 1963, 89 (381) :339-348
[56]   Eddy covariance fluxes of peroxyacetyl nitrates (PANs) and NOy to a coniferous forest -: art. no. D09304 [J].
Turnipseed, AA ;
Huey, LG ;
Nemitz, E ;
Stickel, R ;
Higgs, J ;
Tanner, DJ ;
Slusher, DL ;
Sparks, JP ;
Flocke, F ;
Guenther, A .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2006, 111 (D9)
[57]   Measured atmospheric new particle formation rates: Implications for nucleation mechanisms [J].
Weber, RJ ;
Marti, JJ ;
McMurry, PH ;
Eisele, FL ;
Tanner, DJ ;
Jefferson, A .
CHEMICAL ENGINEERING COMMUNICATIONS, 1996, 151 :53-64
[58]   The contribution of sulfuric acid and non-volatile compounds on the growth of freshly formed atmospheric aerosols -: art. no. L17810 [J].
Wehner, B ;
Petäjä, T ;
Boy, M ;
Engler, C ;
Birmili, W ;
Tuch, T ;
Wiedensohler, A ;
Kulmala, M .
GEOPHYSICAL RESEARCH LETTERS, 2005, 32 (17) :1-4