The aqueous flux of inorganic Hg and monomethyl Hg from sediments to the wa
ter column was determined at several sites in Lavaca Bay, an estuary along
the Texas Coast, historically impacted by Hg discharges. Diffusive fluxes w
ere calculated at 15 sites using interstitial pore water gradients and comp
ared to direct flux measurements obtained at two sites using benthic flux c
hambers. 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 MMH
g fluxes varied seasonally; maximal fluxes occurred in late winter to early
spring. Flux chamber deployments at an impacted site revealed that MMHg wa
s 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 MMH
g 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 biolog
ical and/or chemical processes near the sediment-water interface were stron
gly mediating the sediment-water exchange of MMHg.