Sediment-water fluxes of mercury in Lavaca Bay, Texas

被引:144
作者
Gill, GA
Bloom, NS
Cappellino, S
Driscoll, CT
Dobbs, C
McShea, L
Mason, R
Rudd, JWM
机构
[1] Texas A&M Univ, Dept Oceanog, Lab Oceanog & Environm Res, Galveston, TX 77551 USA
[2] Frontier Geosci Inc, Seattle, WA 98109 USA
[3] Parametrix Inc, Houston, TX 77099 USA
[4] Syracuse Univ, Dept Civil & Environm Engn, Syracuse, NY 13244 USA
[5] ALCOA, Point Comfort, TX 77978 USA
[6] Univ Maryland, Chesapeake Biol Lab, Solomons, MD 20688 USA
[7] Fisheries & Oceans Canada, Inst Freshwater, Winnipeg, MB R3T 2N6, Canada
关键词
D O I
10.1021/es980380c
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The aqueous flux of inorganic Hg and monomethyl Hg from sediments to the water column was determined at several sites in Lavaca Bay, an estuary along the Texas Coast, historically impacted by Hg discharges. Diffusive fluxes were calculated at 15 sites using interstitial pore water gradients and compared to direct flux measurements obtained at two sites using benthic flux chambers. The diffusive flux of monomethyl mercury (MMHg), when modeled as a chloride species, varied over 3 orders of magnitude from 0.2 to 1500 ng m(-2) day(-1). Diffusive fluxes determined at a single site revealed that MMHg fluxes varied seasonally; maximal fluxes occurred in late winter to early spring. Flux chamber deployments at an impacted site revealed that MMHg was the Hg species entering the water column from sediments and the flux was not in steady-state; there was a strong diurnal signal with most of the MMHg flux occurring during dark periods. The flux of inorganic Hg was smaller and not as easily discernible by this method. The MMHg flux during the dark period (830 ng m(-2) day(-1)) was about 6 times greater than the estimated diffusional flux (140 ng m(-2) day(-1)) for MMHgCl, suggesting that biological and/or chemical processes near the sediment-water interface were strongly mediating the sediment-water exchange of MMHg.
引用
收藏
页码:663 / 669
页数:7
相关论文
共 32 条
[1]   SEASONAL-VARIATIONS IN PRODUCTION AND CONSUMPTION RATES OF DISSOLVED ORGANIC-CARBON IN AN ORGANIC-RICH COASTAL SEDIMENT [J].
ALPERIN, MJ ;
ALBERT, DB ;
MARTENS, CS .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1994, 58 (22) :4909-4930
[2]   Behavior of mercury in the Patuxent River estuary [J].
Benoit, JM ;
Gilmour, CC ;
Mason, RP ;
Riedel, GS ;
Riedel, GF .
BIOGEOCHEMISTRY, 1998, 40 (2-3) :249-265
[4]   Speciation and cycling of mercury in Lavaca Bay, Texas, sediments [J].
Bloom, NS ;
Gill, GA ;
Cappellino, S ;
Dobbs, C ;
McShea, L ;
Driscoll, C ;
Mason, R ;
Rudd, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (01) :7-13
[5]   DETERMINATION OF MERCURY IN SEAWATER AT SUB-NANOGRAM PER LITER LEVELS [J].
BLOOM, NS ;
CRECELIUS, EA .
MARINE CHEMISTRY, 1983, 14 (01) :49-59
[6]   RATE OF MERCURY LOSS FROM CONTAMINATED ESTUARINE SEDIMENTS [J].
BOTHNER, MH ;
JAHNKE, RA ;
PETERSON, ML ;
CARPENTER, R .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1980, 44 (02) :273-285
[7]   The diffusive tortuosity of fine-grained unlithified sediments [J].
Boudreau, BP .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (16) :3139-3142
[8]  
GAYNON C, 1996, LIMNOL OCEANOGR, V41, P428
[9]   MERCURY METHYLATION IN AQUATIC SYSTEMS AFFECTED BY ACID DEPOSITION [J].
GILMOUR, CC ;
HENRY, EA .
ENVIRONMENTAL POLLUTION, 1991, 71 (2-4) :131-169
[10]   Methylmercury concentrations and production rates across a trophic gradient in the northern Everglades [J].
Gilmour, CC ;
Riedel, GS ;
Ederington, MC ;
Bell, JT ;
Benoit, JM ;
Gill, GA ;
Stordal, MC .
BIOGEOCHEMISTRY, 1998, 40 (2-3) :327-345