Evasion of mercury from coastal and open waters of the Atlantic Ocean and the Mediterranean Sea

被引:111
作者
Gårdfeldt, K
Sommar, J
Ferrara, R
Ceccarini, C
Lanzillotta, E
Munthe, J
Wängberg, I
Lindqvist, O
Pirrone, N
Sprovieri, F
Pesenti, E
Strömberg, D
机构
[1] Gothenburg Univ, Dept Chem, S-41296 Gothenburg, Sweden
[2] CNR, Inst Biophys, Area Ric, I-56010 Ghezzano, Pisa, Italy
[3] Swedish Environm Res Inst, IVL, S-40258 Gothenburg, Sweden
[4] CNR, Inst Atmospher Pollut, I-87036 Arcavacata Di Rende, Italy
[5] Gothenburg Univ, Dept Environm & Conservat Sci, S-41296 Gothenburg, Sweden
关键词
emissions; mercury; DGM; natural sources; anthropogenic sources; biogeochemical; Mediterranean Sea;
D O I
10.1016/S1352-2310(03)00238-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Dissolved gaseous mercury (DGM) was measured in coastal Atlantic seawater and in the Mediterranean Sea. The Atlantic measurements were performed during September 1999 at the Mace Head Atmospheric Research Station, situated on the Irish west coast. The measurements in the Mediterranean Sea were made along a 6000km cruise path from 14 July to 9 August 2000 in the framework of the Med-Oceanor project. Total gaseous mercury (TGM) concentrations in air were continuously measured with a 5 min time resolution using an automated mercury analyser (Tekran 2537A) during both expeditions. Paired TGM and DGM samples from all campaigns showed that the Surface water was supersaturated with elemental mercury. The mercury evasion was estimated using a gas exchange model (J. Geophys. Res. 97 (1992) 7373), which uses salinity, wind speed and water temperature as independent parameters. The predicted average mercury evasion from the coastal Atlantic water was 2.7ng m(-2) h(-1) implying that the concentration of TGM in the Atlantic air is enhanced by mercury evasion from the sea. Measurements in different regions of the Mediterranean Sea showed spatial variations in DGM concentrations. The highest DGM concentration (similar to90 pg l(-1)) was observed at a location in the Strait of Sicily (37degrees16N 11degrees52E). The mercury evasion in the eastern sector of the Mediterranean Sea (area: 32-36degreesN, 17-28degreesE) was generally higher (7.9 ng m(-2) h(-1)) than that observed in the Tyrrhenian Sea (4.2 ng m(-2) h(-1)) or in the western sector (2.5 ng m(-2) h(-1)) (areas: 38-42degreesN, 8-13degreesE and 38-41degreesN, 7-8degreesE, respectively). Estimations of mercury evasion were also made at Mediterranean coastal sites using a dynamic chamber technique. In addition, a newly developed method making continuous in situ DGM measurements possible was tested. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
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页码:S73 / S84
页数:12
相关论文
共 55 条
[1]   ABIOTIC REDUCTION OF MERCURY BY HUMIC SUBSTANCES IN AQUATIC SYSTEM - AN IMPORTANT PROCESS FOR THE MERCURY CYCLE [J].
ALLARD, B ;
ARSENIE, I .
WATER AIR AND SOIL POLLUTION, 1991, 56 :457-464
[2]   Distribution and transformation of elemental mercury in the St. Lawrence River and Lake Ontario [J].
Amyot, M ;
Lean, DRS ;
Poissant, L ;
Doyon, MR .
CANADIAN JOURNAL OF FISHERIES AND AQUATIC SCIENCES, 2000, 57 :155-163
[3]  
[Anonymous], 1991, PRINCIPLES ENV TOXIC
[4]  
Asher W. E., 1995, AIR WATER GAS TRANSF, P227
[5]   Elemental mercury concentrations and formation rates in the Scheldt estuary and the North Sea [J].
Baeyens, W ;
Leermakers, M .
MARINE CHEMISTRY, 1998, 60 (3-4) :257-266
[6]   DETERMINATION OF VOLATILE MERCURY SPECIES AT THE PICOGRAM LEVEL BY LOW-TEMPERATURE GAS-CHROMATOGRAPHY WITH COLD-VAPOR ATOMIC FLUORESCENCE DETECTION [J].
BLOOM, N ;
FITZGERALD, WF .
ANALYTICA CHIMICA ACTA, 1988, 208 (1-2) :151-161
[7]   THE BEHAVIOR OF MERCURY IN THE PHYSICAL-ENVIRONMENT [J].
BROSSET, C .
WATER AIR AND SOIL POLLUTION, 1987, 34 (02) :145-166
[8]   The distribution and cycling of mercury species in the western Mediterranean [J].
Cossa, D ;
Martin, JM ;
Takayanagi, K ;
Sanjuan, J .
DEEP-SEA RESEARCH PART II-TOPICAL STUDIES IN OCEANOGRAPHY, 1997, 44 (3-4) :721-740
[9]  
Cossa D, 1996, NATO ASI 2, V21, P229
[10]   Photoreduction of mercury in sea water and its possible implications for Hg0 air-sea fluxes [J].
Costa, M ;
Liss, PS .
MARINE CHEMISTRY, 1999, 68 (1-2) :87-95