Influence of the source formulation on modeling the atmospheric global distribution of sea salt aerosol

被引:111
作者
Guelle, W
Schulz, M
Balkanski, Y
Dentener, F
机构
[1] CEA, CNRS, Lab Sci Climat & Environm, F-91191 Gif Sur Yvette, France
[2] European Commiss, Joint Res Ctr, I-21020 Ispra, Italy
关键词
D O I
10.1029/2001JD900249
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Three different sea salt generation functions are investigated for use in global three-dimensional atmospheric models. Complementary observational data are used to validate an annual simulation of the whole size range (film, jet, and spume droplet derived particles). Aerosol concentrations are corrected for humidity growth and sampler inlet characteristics. Data from the North American deposition network are corrected for mineral dust to derive sea salt wet fluxes. We find that sea salt transport to inner continental areas requires substantial mass in the jet droplet range, which is best reproduced with the source of Monahan et al. [1986]. The results from this source formulation also shows the best agreement with aerosol concentration seasonality and sea salt size distributions below 4 mum dry radius. Measured wind speed dependence of coarse particle occurrence suggests that above 4 mum the source from Smith and Harrison [1998] is most appropriate. Such sea salt simulations are relevant for assessing heterogeneous chemistry and radiative effects. Sea salt aerosol provides on an annual average, in marine regions, an aggregate surface area equal to 1-10% of the area of the underlying Earth's surface. Together with mineral dust, sulfate, and carbonaceous aerosol the total aerosol surface area globally amounts to 13% of that of the Earth's surface. On the basis of atmospheric column burdens, sea salt represents 21% of the total global aerosol surface area. Equal partitioning of the aerosol surface area among the four components suggests that one has to consider all of them if the global aerosol impact is to be fully determined.
引用
收藏
页码:27509 / 27524
页数:16
相关论文
共 69 条
[1]   THE SPRAY CONTRIBUTION TO NET EVAPORATION FROM THE SEA - A REVIEW OF RECENT PROGRESS [J].
ANDREAS, EL ;
EDSON, JB ;
MONAHAN, EC ;
ROUAULT, MP ;
SMITH, SD .
BOUNDARY-LAYER METEOROLOGY, 1995, 72 (1-2) :3-52
[2]   SEA SPRAY AND THE TURBULENT AIR-SEA HEAT FLUXES [J].
ANDREAS, EL .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1992, 97 (C7) :11429-11441
[3]  
Andreas EL, 1998, J PHYS OCEANOGR, V28, P2175, DOI 10.1175/1520-0485(1998)028<2175:ANSSGF>2.0.CO
[4]  
2
[5]   Production and decay of ClNO2, from the reaction of gaseous N2O5 with NaCl solution: Bulk and aerosol experiments [J].
Behnke, W ;
George, C ;
Scheer, V ;
Zetzsch, C .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D3) :3795-3804
[6]  
BLANCHARD DC, 1984, TELLUS B, V36, P118, DOI 10.1111/j.1600-0889.1984.tb00233.x
[7]   Seasonal variation of aerosol composition at Cheju Island, Korea [J].
Carmichael, GR ;
Zhang, Y ;
Chen, LL ;
Hong, MS ;
Ueda, H .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (13) :2407-2416
[8]   AQUEOUS-PHASE CHEMICAL PROCESSES IN DELIQUESCENT SEA-SALT AEROSOLS - A MECHANISM THAT COUPLES THE ATMOSPHERIC CYCLES OF S AND SEA SALT [J].
CHAMEIDES, WL ;
STELSON, AW .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D18) :20565-20580
[9]   Modeling the mineralogy of atmospheric dust sources [J].
Claquin, T ;
Schulz, M ;
Balkanski, YJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D18) :22243-22256
[10]  
CLAQUIN T, 1999, THESIS U PARIS VI FB