Chasing quicksilver:: Modeling the atmospheric lifetime of Hg0(g) in the marine boundary layer at various latitudes

被引:77
作者
Hedgecock, IM [1 ]
Pirrone, N [1 ]
机构
[1] CNR, Inst Atmospher Pollut, UNICAL, I-87036 Arcavacata Di Rende, Italy
关键词
D O I
10.1021/es034623z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The lifetime of elemental mercury in the marine boundary layer (MBL) has been studied using AMCOTS (Atmospheric Mercury Chemistry Over The Sea), a box model of MBL photochemistry including aerosols and detailed mercury chemistry. Recently measured Hg-(g)(0) oxidation reactions have been included, and the studies were performed as a function of latitude, time of year, boundary layer liquid water content (LWC) and cloud optical depth. The results show that Hg has the shortest lifetime when air temperatures are low and sunlight and deliquescent aerosol particles are plentiful. Thus the modeled lifetime for clear-sky conditions is actually shorter at mid-latitudes and high latitudes than near the equator, and for a given latitude and time of year, cooler temperatures enhance the rate of Hg oxidation. Under typical summer conditions (for a given latitude) of temperature and cloudiness, the lifetime (tau) of Hg-(g)(0) in the MBL is calculated to be around 10 days at all latitudes between the equator and 60degrees N. This is much shorter than the generally accepted atmospheric residence time for Hg-(g)(0) of a year or more. Given the relatively stable background concentrations of Hg-(g)(0) which have been measured, continual replenishment of Hg-(g)(0) must take place, suggesting a "multihop" mechanism for the distribution of Hg, rather than solely aeolian transport with little or no chemical transformation between source and receptor. Inclusion of an empirical Hg-(g)(0) emission factor related to insolation was used to stabilize the Hg-(g)(0) concentration in the model, and the emission rates necessarily agree well with estimated emission fluxes for the open ocean.
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页码:69 / 76
页数:8
相关论文
共 29 条
[1]  
[Anonymous], 2001, WATER AIR SOIL POLL, DOI DOI 10.1023/A:1013171509022
[2]   Reactions of gaseous mercury with atomic and molecular halogens: Kinetics, product studies, and atmospheric implications [J].
Ariya, PA ;
Khalizov, A ;
Gidas, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (32) :7310-7320
[3]   Vertical distribution of gaseous elemental mercury in Canada [J].
Banic, CM ;
Beauchamp, ST ;
Tordon, RJ ;
Schroeder, WH ;
Steffen, A ;
Anlauf, KA ;
Wong, HKT .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2003, 108 (D9)
[4]   Gas phase elemental mercury: a comparison of LIF detection techniques and study of the kinetics of reaction with the hydroxyl radical [J].
Bauer, D ;
D'Ottone, L ;
Campuzano-Jost, P ;
Hynes, AJ .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2003, 157 (2-3) :247-256
[5]  
European Commission, 2001, AMB AIR POLL MERC PO
[6]   Evasion of mercury from coastal and open waters of the Atlantic Ocean and the Mediterranean Sea [J].
Gårdfeldt, K ;
Sommar, J ;
Ferrara, R ;
Ceccarini, C ;
Lanzillotta, E ;
Munthe, J ;
Wängberg, I ;
Lindqvist, O ;
Pirrone, N ;
Sprovieri, F ;
Pesenti, E ;
Strömberg, D .
ATMOSPHERIC ENVIRONMENT, 2003, 37 :S73-S84
[7]   Reactive gaseous mercury in the marine boundary layer: modelling and experimental evidence of its formation in the Mediterranean region [J].
Hedgecock, IM ;
Pirrone, N ;
Sprovieri, F ;
Pesenti, E .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (37) :S41-S49
[8]   Mercury and photochemistry in the marine boundary layer-modelling studies suggest the in situ production of reactive gas phase mercury [J].
Hedgecock, IM ;
Pirrone, N .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (17) :3055-3062
[9]  
*ISCCP, 2002, INT SAT CLOUD CLIM P
[10]   The atmospheric cycling and air-sea exchange of mercury species in the South and equatorial Atlantic Ocean [J].
Lamborg, CH ;
Rolfhus, KR ;
Fitzgerald, WF ;
Kim, G .
DEEP-SEA RESEARCH PART II-TOPICAL STUDIES IN OCEANOGRAPHY, 1999, 46 (05) :957-977