Five field trips were conducted in the San Francisco Bay-Delta between May 2000 and October 2001 to investigate the sediment-water exchange of total mercury (Hg) and monomethyl mercury (MMHg). Solid-phase Hg averaged ϳ1 nmol g Ϫ1 and did not show any variability with depth or time or among sites. In contrast, solid-phase MMHg showed considerable vertical, temporal, and spatial variability (0.4-66 pmol g Ϫ1 ), with the highest values occurring at a peat-rich environment in May 2001, suggesting that MMHg production was largely controlled by temporal factors and habitat type. In pore water, both Hg and MMHg concentrations were generally elevated near the sediment-water interface during warm months. Sediment-water exchange flux of MMHg, determined with benthic chamber deployments, ranged from Ϫ92 to 850 pmol m Ϫ2 d Ϫ1 , with higher values occurring in May. In most cases, diffusional fluxes of Hg and MMHg, estimated with the use of interfacial concentration gradients, constituted only a minor portion of the measured fluxes, suggesting the importance of advective processes on sediment-water exchange. Surface-water transect and time series studies conducted in Franks Tract support the commonly held belief that wetland and marsh regions are major sources for MMHg within the Delta. The integrated sediment-water fluxes of Hg and MMHg in the study area were estimated to be 130 and 6 mmol d Ϫ1 , respectively, and the benthic input was as important a source of Hg and MMHg as the riverine input within the Delta during low-flow months.

We assessed monomethylmercury (MeHg) dynamics in a tidal wetland over three seasons using a novel method that employs a combination of in situ optical measurements as concentration proxies. MeHg concentrations measured over a single spring tide were extended to a concentration time series using in situ optical measurements. Tidal fluxes were calculated using modeled concentrations and bi-directional velocities obtained acoustically. The magnitude of the flux was the result of complex interactions of tides, geomorphic features, particle sorption, and random episodic events such as wind storms and precipitation. Correlation of dissolved organic matter quality measurements with timing of MeHg release suggests that MeHg is produced in areas of fluctuating redox and not limited by buildup of sulfide. The wetland was a net source of MeHg to the estuary in all seasons, with particulate flux being much higher than dissolved flux, even though dissolved concentrations were commonly higher. Estimated total MeHg yields out of the wetland were approximately 2.5 mg m 22 yr 21 -4-40 times previously published yields-representing a potential loading to the estuary of 80 g yr 21 , equivalent to 3% of the river loading. Thus, export from tidal wetlands should be included in mass balance estimates for MeHg loading to estuaries. Also, adequate estimation of loads and the interactions between physical and biogeochemical processes in tidal wetlands might not be possible without long-term, high-frequency in situ measurements.

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Recent studies indicate significant amounts of mercury (Hg) are annually transported into the San Francisco Bay-Delta (Bay-Delta) as a result of historic gold and Hg mining activities. We examined temporal and spatial variation in concentrations of total Hg (Hg(T)) and monomethylmercury (MMHg) in surficial sediments of various ecosystem types in the Bay-Delta. We sampled surficial sediments across the Bay-Delta system and found Hg(T) sediment concentrations in the central Delta were generally 100-200 ng g(-1) and increased westward through Suisun Bay to 250-350 ng g(-1). MMHg concentrations in the central Delta were between 1 and 3 ng g(-1), while those in sediments in the perimeter waterways and adjacent bays were less than 1 ng g(-1). Six sites were monitored monthly for over a year to identify seasonal changes in Hg sediment concentrations. Hgtau sediment concentrations ranged from 48 to 382 ng g(-1) and varied as a function of location not season. However, MMHg concentrations varied seasonally, increasing from 1 ng g(-1) during winter months to 6 ng g(-1) during spring and summer. Transects conducted at three marshes in the central Delta revealed MMHg sediment concentrations of 4-8 ng g(-1) at the interior and 2 ng g(-1) at the exterior of the marshes. Habitat type was a major factor controlling MMHg concentration and the MMHg to Hg(T) ratio in sediments of the Bay-Delta. MMHg was significantly correlated to Hgt (r2 = 0.49) in marsh sediments.

Total mercury (HgT) and monomethyl mercury (MMHg) concentrations in fog collected from 4 locations in and around Monterey Bay, California during June‐August of 2011 were 10.7 ± 6.8 and 3.4 ± 3.8 ng L−1respectively. In contrast, mean HgT and MMHg concentrations in rain water from March‐June, 2011 were 1.8 ± 0.9 and 0.1 ± 0.04 ng L−1 respectively. Using estimates of fog water deposition from 6 sites in the region using a standard fog water collector (SFC), depositions of HgT and MMHg via fog were found to range from 42–4600 and 14–1500 ng m−2 y−1, which accounted for 7–42% of HgT and 61–99% of MMHg in total atmospheric deposition (fog, rain, and dry deposition), estimated for the coastal area. These initial measurements suggest that fog precipitation may constitute an important but previously overlooked input of MMHg to coastal environments. Preliminary comparisons of these data with associated chemical, meteorological and oceanic data suggest that biotically formed MMHg from coastal upwelling may contribute to the MMHg in fog water.