Reactive gaseous mercury in the marine boundary layer: modelling and experimental evidence of its formation in the Mediterranean region

被引:46
作者
Hedgecock, IM [1 ]
Pirrone, N [1 ]
Sprovieri, F [1 ]
Pesenti, E [1 ]
机构
[1] UNICAL, CNR, Inst Atmospher Pollut, I-87036 Arcavacata Di Rende, Italy
关键词
atmospheric mercury; reactive gaseous mercury; Mediterranean; modelling; MBL;
D O I
10.1016/S1352-2310(03)00236-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Reactive gaseous mercury (RGM) concentrations have been modelled using a photochemical box model of the marine boundary layer (MBL) and compared to measured data obtained during a research cruise. The model has been constrained by using measured concentrations of elemental Hg and ozone, as well as measured temperature and relative humidity. The results show good qualitative agreement both during the rough weather encountered on the first part of the voyage and the second, calmer period of the campaign. Quantitative agreement is obtained using a box height of 100m during the first leg of the campaign. The modelled and measured results from the second leg agree as far as the nocturnal RGM concentration minima are concerned but underestimate the daytime maxima by a factor of two. The comparison of the modelled with measured results supports the hypothesis that there are daytime mercury oxidation reactions occurring which have not yet been identified. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:S41 / S49
页数:9
相关论文
共 27 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]   Oxidation of elemental mercury in the atmosphere; Constraints imposed by global scale modelling [J].
Bergan, T ;
Rodhe, H .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2001, 40 (02) :191-212
[4]   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
[5]  
HEDGECOCK IM, 2001, P 8 EUR S PHYS CHEM
[6]   On the long-range transport of air pollutants from Europe to Africa [J].
Kallos, G ;
Kotroni, V ;
Lagouvardos, K ;
Papadopoulos, A .
GEOPHYSICAL RESEARCH LETTERS, 1998, 25 (05) :619-622
[7]   Development and characterization of an annular denuder methodology for the measurement of divalent inorganic reactive gaseous mercury in ambient air [J].
Landis, MS ;
Stevens, RK ;
Schaedlich, F ;
Prestbo, EM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (13) :3000-3009
[8]   Observation of filterable bromine variabilities during Arctic tropospheric ozone depletion events in high (1hour) time resolution [J].
Langendörfer, U ;
Lehrer, E ;
Wagenbach, D ;
Platt, U .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1999, 34 (01) :39-54
[9]   Aqueous phase reactions of mercury with free radicals and chlorine: Implications for atmospheric mercury chemistry [J].
Lin, CJ ;
Pehkonen, SO .
CHEMOSPHERE, 1999, 38 (06) :1253-1263
[10]   Aqueous free radical chemistry of mercury in the presence of iron oxides and ambient aerosol [J].
Lin, CJ ;
Pehkonen, SO .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (24) :4125-4137