Mercury and Methylmercury Dynamics in a Coastal Plain Watershed, New Jersey, USA

被引:23
作者
Barringer, Julia L. [1 ]
Riskin, Melissa L. [1 ]
Szabo, Zoltan [1 ]
Reilly, Pamela A. [1 ]
Rosman, Robert [1 ]
Bonin, Jennifer L. [1 ]
Fischer, Jeffrey M. [1 ]
Heckathorn, Heather A. [1 ]
机构
[1] US Geol Survey, W Trenton, NJ 08628 USA
关键词
Mercury; Methylmercury; Wetlands; Streamwater; Groundwater; Land use; DISSOLVED ORGANIC-CARBON; SOUTHERN NEW-JERSEY; IN-GROUND WATER; NORTHERN WISCONSIN; FLORIDA EVERGLADES; HUMIC SUBSTANCES; TRANSPORT; MATTER; DEPOSITION; CHEMISTRY;
D O I
10.1007/s11270-010-0340-1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The upper Great Egg Harbor River watershed in New Jersey's Coastal Plain is urbanized but extensive freshwater wetlands are present downstream. In 2006-2007, studies to assess levels of total mercury (THg) found concentrations in unfiltered streamwater to range as high as 187 ng/L in urbanized areas. THg concentrations were < 20 ng/L in streamwater in forested/wetlands areas where both THg and dissolved organic carbon concentrations tended to increase while pH and concentrations of dissolved oxygen and nitrate decreased with flushing of soils after rain. Most of the river's flow comes from groundwater seepage; unfiltered groundwater samples contained up to 177 ng/L of THg in urban areas where there is a history of well water with THg that exceeds the drinking water standard (2,000 ng/L). THg concentrations were lower (< 25 ng/L) in unfiltered groundwater from downstream wetland areas. In addition to higher THg concentrations (mostly particulate), concentrations of chloride were higher in streamwater and groundwater from urban areas than in those from downstream wetland areas. Methylmercury (MeHg) concentrations in unfiltered streamwater ranged from 0.17 ng/L at a forest/wetlands site to 2.94 ng/L at an urban site. The percentage of THg present as MeHg increased as the percentage of forest + wetlands increased, but also was high in some urban areas. MeHg was detected only in groundwater < 1 m below the water/sediment interface. Atmospheric deposition is presumed to be the main source of Hg to the wetlands and also may be a source to groundwater, where wastewater inputs in urban areas are hypothesized to mobilize Hg deposited to soils.
引用
收藏
页码:251 / 273
页数:23
相关论文
共 67 条
[1]  
*AC NAT SCI, 1994, 9315F AC NAT SCI
[2]  
BAE Systems, 2003, BAE SYST ADR DIG COL
[3]   Redox chemistry in Minnesota streams during episodes of increased methylmercury discharge [J].
Balogh, SJ ;
Nollet, YH ;
Swain, EB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (19) :4921-4927
[4]   Effects of dissolved organic carbon and salinity on bioavailability of mercury [J].
Barkay, T ;
Gillman, M ;
Turner, RR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) :4267-4271
[5]  
Barringer J.L., 1997, 95475 US GEOL SURV
[6]   Mercury concentrations in water from an unconfined aquifer system, New Jersey coastal plain [J].
Barringer, JL ;
Szabo, Z ;
Kauffman, LJ ;
Barringer, TH ;
Stackelberg, PE ;
Ivahnenko, T ;
Rajagopalan, S ;
Krabbenhoft, DP .
SCIENCE OF THE TOTAL ENVIRONMENT, 2005, 346 (1-3) :169-183
[7]   Overview of investigations into mercury in ground water, soils, and septage, New Jersey coastal plain [J].
Barringer, Julia L. ;
Szabo, Zoltan .
WATER AIR AND SOIL POLLUTION, 2006, 175 (1-4) :193-221
[8]   Mercury in ground water, septage, leach-field effluent, and soils in residential areas, New Jersey coastal plain [J].
Barringer, Julia L. ;
Szabo, Zoltan ;
Schneider, Donald ;
Atkinson, William D. ;
Gallagher, Robert A. .
SCIENCE OF THE TOTAL ENVIRONMENT, 2006, 361 (1-3) :144-162
[9]   THE EFFECTS OF PH AND CHLORIDE CONCENTRATION ON MERCURY SORPTION .1. BY GOETHITE [J].
BARROW, NJ ;
COX, VC .
JOURNAL OF SOIL SCIENCE, 1992, 43 (02) :295-304
[10]  
BELT K, 2008, NAT WAT QUAL MON COU