Total gaseous mercury concentration and flux over a coastal saltmarsh vegetation in Connecticut, USA

被引:49
作者
Lee, X [1 ]
Benoit, G [1 ]
Hu, XZ [1 ]
机构
[1] Yale Univ, Sch Forestry & Environm Studies, New Haven, CT 06511 USA
关键词
gaseous mercury; mercury cycle; wetland; S; patens; Long Island sound; micrometeorology; evapotranspiration;
D O I
10.1016/S1352-2310(99)00487-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The objective of this study is to characterize the ambient total gaseous mercury (TGM) concentration (C) at a coastal salt marsh and the TGM flux (F) between the marsh and the atmosphere using data collected on a near-continuous basis from 5 Jun to 8 July, 1997 and from 8 March to 23 July, 1998. In general, C was lower in the afternoon than at night, which is believed to be a result of diurnal variation in the mixing efficiency of the atmospheric boundary layer. The lack of a significant upward trend from March to July 1998 implies that TGM was removed from the boundary layer at a rate equal or greater than the surface emission. Three episodes of low C (0-1 ng m(-3)) occurred in July 1998, each lasting about 3 h. The TGM flux, F, was determined with the micrometeorological aerodynamic method. An episodic event of large positive F (emission) occurred in early spring of 1998 and appears to have been triggered by ice melting. It is proposed that three competing mechanisms - Hg vaporization, oxygen transport via roots, and diffusion into plants via stomata - may have played a role in the Hg exchange over other periods, resulting in bi-directional exchange of Hg with the atmosphere. Extrapolation of the 1998 data to the whole year suggests a weak sink removing 4 +/- 7 mu g Hg m(-2) yr(-1) from the atmosphere, a rate similar in magnitude to wet or particulate deposition to the site but much smaller than the rate of Hg accumulation in the sediment. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4205 / 4213
页数:9
相关论文
共 48 条
[1]   Radiosonde boundary layer budgets above a boreal forest [J].
Barr, AG ;
Betts, AK .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D24) :29205-29212
[2]   FORMATION OF METHYL MERCURY FROM PURE MERCURIC SULPHIDE IN AEROBIC ORGANIC SEDIMENT [J].
FAGERSTR.T ;
JERNELOV, A .
WATER RESEARCH, 1971, 5 (03) :121-&
[3]  
Fitzgerald W., 1983, TRACE METALS SEA WAT
[4]  
Fitzgerald W.F., 1989, CHEM OCEANOGR, P151
[5]   ATMOSPHERIC CYCLING AND AIR-WATER EXCHANGE OF MERCURY OVER MIDCONTINENTAL LACUSTRINE REGIONS [J].
FITZGERALD, WF ;
MASON, RP ;
VANDAL, GM .
WATER AIR AND SOIL POLLUTION, 1991, 56 :745-767
[6]   HIGH-LEVELS OF MERCURY CONTAMINATION IN MULTIPLE MEDIA OF THE CARSON RIVER DRAINAGE-BASIN OF NEVADA - IMPLICATIONS FOR RISK ASSESSMENT [J].
GUSTIN, MS ;
TAYLOR, GE ;
LEONARD, TL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 (09) :772-778
[7]   Effect of temperature and air movement on the flux of elemental mercury from substrate to the atmosphere [J].
Gustin, MS ;
Taylor, GE ;
Maxey, RA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D3) :3891-3898
[8]   THE GAS-PHASE OXIDATION OF ELEMENTAL MERCURY BY OZONE [J].
HALL, B .
WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) :301-315
[9]   FOLIAR EXCHANGE OF MERCURY-VAPOR - EVIDENCE FOR A COMPENSATION POINT [J].
HANSON, PJ ;
LINDBERG, SE ;
TABBERER, TA ;
OWENS, JG ;
KIM, KH .
WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) :373-382
[10]  
HE H, 1998, THESIS YALE U