Modeling sea-salt aerosols in the atmosphere .2. Atmospheric concentrations and fluxes

被引:105
作者
Gong, SL
Barrie, LA
Prospero, JM
Savoie, DL
Ayers, GP
Blanchet, JP
Spacek, L
机构
[1] UNIV MIAMI, ROSENSTIEL SCH MARINE & ATMOSPHER SCI, MIAMI, FL 33149 USA
[2] CSIRO, DIV ATMOSPHER RES, MORDIALLOC, VIC 3195, AUSTRALIA
[3] UNIV QUEBEC, DIV EARTH SCI, MONTREAL, PQ H3C 3P8, CANADA
关键词
D O I
10.1029/96JD03401
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Atmospheric sea-salt aerosol concentrations are studied using both long-term observations and model simulations of Na+ at seven stations around the globe. Good agreement is achieved between observations and model predictions in the northern hemisphere. A stronger seasonal variation occurs in the high-latitude North Atlantic than in regions close to the equator and in high-latitude southern hemisphere. Generally, concentrations are higher for both boreal and austral winters. With the model, the production flux and removal flux at the atmosphere-ocean interface was calculated and used to estimate the global sea-salt budget. The flux also shows seasonal variation similar to that of sea-salt concentration. Depending on the geographic location, the model predicts that dry deposition accounts for 60-70% of the total sea-salt removed from the atmosphere while in-cloud and below-cloud precipitation scavenging accounts for about 1% and 28-39% of the remainder, respectively. The total amount of sea-salt aerosols emitted from the world oceans to the atmosphere is estimated to be in the vicinity of 1.17 X 10(16) g yr(-1). Approximately 99% of the sea-salt aerosol mass generated by wind falls back to the sea with about 1-2% remaining in the atmosphere to be exported from the original grid square (300 x 300 km). Only a small portion of that exported (similar to 4%) is associated with submicron particles that are likely to undergo long-range transport.
引用
收藏
页码:3819 / 3830
页数:12
相关论文
共 21 条
[1]   CHEMICAL-COMPONENTS OF LOWER TROPOSPHERIC AEROSOLS IN THE HIGH ARCTIC - 6 YEARS OF OBSERVATIONS [J].
BARRIE, LA ;
BARRIE, MJ .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1990, 11 (03) :211-226
[2]   ARCTIC AEROSOL SIZE-SEGREGATED CHEMICAL OBSERVATIONS IN RELATION TO OZONE DEPLETION DURING POLAR SUNRISE EXPERIMENT 1992 [J].
BARRIE, LA ;
STAEBLER, R ;
TOOM, D ;
GEORGI, B ;
DENHARTOG, G ;
LANDSBERGER, S ;
WU, D .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D12) :25439-25451
[3]  
Barrie LA, 1995, NATO ASI SER SER I, V30, P1
[4]  
Baumgartner A., 1975, The world water balance: Mean annual global continental and maritime precipitation, evaporation and run-off
[5]  
Blanchard D.C., 1963, Prog. Oceanogr, V1, P71, DOI [DOI 10.1016/0079-6611, 10.1016/0079-6611(63)90004-1, DOI 10.1016/0079-6611(63)90004-1]
[6]   SEASONAL ESTIMATES OF GLOBAL ATMOSPHERIC SEA-SALT DISTRIBUTIONS [J].
ERICKSON, DJ ;
MERRILL, JT ;
DUCE, RA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1986, 91 (D1) :1067-1072
[7]   ON THE GLOBAL FLUX OF ATMOSPHERIC SEA SALT [J].
ERICKSON, DJ ;
DUCE, RA .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1988, 93 (C11) :14079-14088
[8]   THE YEARLY CIRCULATION OF CHLORIDE AND SULFUR IN NATURE - METEOROLOGICAL, GEOCHEMICAL AND PEDOLOGICAL IMPLICATIONS .1. [J].
ERIKSSON, E .
TELLUS, 1959, 11 (04) :375-403
[9]   THE YEARLY CIRCULATION OF CHLORIDE AND SULFUR IN NATURE - METEOROLOGICAL, GEOCHEMICAL AND PEDOLOGICAL IMPLICATIONS .2. [J].
ERIKSSON, E .
TELLUS, 1960, 12 (01) :63-109
[10]  
Fergusson JE., 1982, INORGANIC CHEM EARTH