Biomonitoring of mercury in the Kastela Bay using transplanted mussels

Kastela Bay, located on the central part of east Adriatic coast, is heavily contaminated by mercury. The main source of contamination was a chlor-alkali plant, which was operating for 40 years since 1949. Previous studies showed that mercury concentrated in the sediment close to the plant is being dispersed throughout the bay by remobilization processes. Subsequent remobilization of mercury buried in the sediment may be harmful to various marine organisms. In order to assess the availability of remobilised mercury to marine organisms and to assess the health risk of consumption of shellfish species from the bay, a monitoring programme was initiated in September 1997. One thousand six hundred specimens of mussels (Mytilus galloprotincialis) of the same size and age, collected in a very clean area, were transferred to four stations in the bay 1.5 m above the sea bottom. Every month during the summer period and every second month in the winter period, 50 mussels were taken from each station for the analysis of mercury and monomethylmercury (MeHg) content. The results obtained during 1 year of biomonitoring suggest that the equilibrium concentration in transplanted mussels was established in a relative short period of time. The digestive gland is preferential organ for the accumulation of total mercury. Seasonal variation of mercury content both in the whole soft tissue, and organs (gills and digestive gland) was observed at all stations. However, methyl mercury is more concentrated in soft tissues than in digestive gland and gills, despite the fact that it is absorbed through these organs. The mercury levels in tissues were below accepted limits for human consumption. Obtained results showed that the implantation of mussels in an area containing sediment contaminated by mercury may be a good monitoring tool for the assessment of the availability of remobilised mercury to marine organisms.     

Mercury distribution in a polluted marine area. Concentrations of methyl mercury in sediments and some marine organisms

Methyl mercury concentrations were measured in various parts of Kastela Bay in the Central Adriatic, which is polluted with inorganic mercury. The values obtained, on a wet weight basis, for sediments were from 2 to 20 micrograms methyl mercury kg-1; for the mussel Mytilus galloprovincialis from 10 to 110 micrograms kg-1; and for various species of fish from 102 to 1448 micrograms kg-1. The methyl mercury content increases by three orders of magnitude going from sediment to fish. The distribution of methyl mercury in relation to the depth of the sediment and the different organs of the mussel is presented. On the basis of the results obtained, it may be concluded that non-migratory species of fish are more suitable for methyl mercury monitoring in the marine environment than are sediment and mussels.     

Methylmercury in rivers draining cultivated watersheds

Total mercury (THg) concentrations in streams draining cultivated watersheds in Minnesota, USA are strongly correlated with total suspended sediment (TSS) concentrations, varying widely in response to precipitation-driven inputs of soil-derived suspended sediments. Methylmercury (MeHg) concentrations in these waterways have not been studied, and little is known about mercury uptake mechanisms in resident fish populations. To begin to identify factors influencing MeHg concentrations and loadings in these streams, we measured THg and MeHg concentrations in unfiltered whole water samples from the Minnesota River and two of its major tributaries, the Blue Earth and Le Sueur Rivers. Land use in the watersheds of these rivers is over 90% row-crop agriculture, and extensive artificial drainage systems deliver runoff and associated solids quickly to local streams and rivers. THg concentrations were elevated (>10 ng/l) during much of Spring 2000 and part of the summer when runoff from precipitation events increased stream discharge and carried soil materials into the streams. Reduced precipitation resulted in low flow conditions from August through October, and THg concentrations decreased to <4.0 ng/l in all three rivers. MeHg concentrations in the Le Sueur River ranged from 0.07 to 0.42 ng/l between June and December. Higher MeHg concentrations (>0.2 ng/l) were measured during summer months when THg and TSS concentrations were high after precipitation events. Elevated MeHg concentrations were also observed in late October after leaf litter inputs. Conditions on the Blue Earth River were different, with elevated MeHg concentrations (>0.5 ng/l) observed during low flow in August and September. These higher concentrations coincided with a period of enhanced microbial growth stimulated by high late-summer temperatures. A late-October increase in MeHg concentration attributed to leaf litter inputs was also observed in this river. MeHg concentration trends in the Minnesota River were similar to those in the Blue Earth River. Indicators of biological productivity (chlorophyll a, volatile suspended solids, and total Kjeldahl nitrogen) were higher in the Blue Earth and Minnesota Rivers compared to the Le Sueur River, which may signal a connection between higher biological activity and increased MeHg concentrations.     

Assessment of mercury and methylmercury pollution with zebra mussel (Dreissena polymorpha) in the Ebro River (NE Spain) impacted by industrial hazardous dumps

Large amounts of industrial waste containing high concentrations of mercury (up to 436 microg/g) are dumped in a reservoir adjacent to a chlor-alkali plant in Flix (Catalonia, Spain), on the lower Ebro River. In order to assess the spatial redistribution of mercury from the point source and its bioavailability to the aquatic food web, zebra mussels (Dreissena polymorpha) were collected at several sites. The highest total Hg (THg) and methylmercury (MeHg) concentrations ever reported for zebra mussels were found (THg: 0.02 to 0.81 microg/g ww; MeHg: 0.22 to 0.60 microg/g ww). At the most polluted site, close to the waste dump, the mean values were 20 times greater than the local background level. Concentrations decreased with increasing mussel size at all sites. The MeHg/THg ratio was ca. 60% (range: 50-80%). A comparison of similar size classes clearly indicated the hot spots of Hg bioavailability to the aquatic food web and downstream transport.     

The burning question: does burning before flooding lower methyl mercury production and bioaccumulation?

Production of methyl mercury (MeHg) is elevated in new hydroelectric reservoirs because organic carbon stimulates methylation of inorganic mercury (Hg) stored in the terrestrial system. This can cause adverse health in fish and in organisms that eat fish. We expected that burning vegetation before flooding would decrease the amount of Hg and organic carbon and thereby lower MeHg production. We conducted a replicated field experiment to investigate the effects of burning vegetation and soil before flooding on MeHg production and bioaccumulation. Vegetation and soil were added to mesocosms in the following combinations: unburned vegetation and unburned soil (Fresh treatments), burned vegetation and unburned soil (Partial Burn treatments), and burned vegetation and burned soil (Complete Burn treatments). Controls had no added vegetation or soil. During combustion with propane torches, a large percentage of the total Hg (THg) and MeHg was lost from vegetation and soil. THg and MeHg concentrations were highest in the surface water of Fresh treatments, lower in Partial Burn treatments and lowest in Complete Burn treatments and controls. Differences in concentrations of MeHg in biota were consistent among treatments, but did not follow aqueous concentrations. On the final sample date, MeHg concentrations in biota of Controls and Partial Burn treatments were greater than in Complete Burn and Fresh treatments. The lack of relationship between MeHg in biota and MeHg in water may have been due to modification of the bioavailability of MeHg by dissolved organic matter as the ratios of MeHg in biota to water were inversely correlated with concentrations of dissolved organic carbon. Although burning before flooding decreased MeHg concentrations in the water, it did not lower MeHg accumulation in the lower food web.     

Horizontal and vertical variability of mercury species in pore water and sediments in small lakes in Ontario

Mary Lake, St. George Lake, and Philips Lake are located in the Greater Toronto Area, Ontario, Canada. These lakes are relatively small and have no direct inflow and outflow channels. Mercury (Hg) input to the lakes comes mainly from atmospheric deposition. Sediment cores from the points of the maximum lake depth and surface sediment samples from the points of maximum lake depth to the bank of each lake were collected in October 2005. Total and methyl mercury concentrations in the pore water and sediments of these samples were determined. In these small lakes with high organic content, there was no correlation between organic content and total mercury (THg) in the samples throughout the entire sediment cores while strong positive correlation between these two parameters was observed in all the surface sediments. Compared with typical methylmercury (MeHg) depth-profiles of sediment cores in other studies, where MeHg concentrations and methylation rates decreased sharply with increasing depth, MeHg distributions in the sediment cores in this study showed that MeHg might have been produced not only in the upper sediment but also in the deeper sediments, which resulted in a larger MeHg reservoir in the sediment. Organic matter, to some extent, affected MeHg distributions in the samples throughout the entire sediment cores. Concentrations of MeHg in all the surface sediments, however, were not controlled by organic matter, whereas they were largely a function of water column depths. Total mercury concentrations in pore water were relatively homogenous in both the sediment cores and surface sediment while MeHg in pore water generally deceased with increasing depth in the sediment cores and increasing distance from the centre of the lakes in surface sediments. Methylmercury contributed 1% to 76% of THg in the pore water samples. Concentrations and distributions of MeHg in overlying water and sediment-surface water in Mary Lake and St. George Lake suggested that both in situ production of MeHg in lake water and the release of MeHg from sediment contributed to high MeHg in deep anoxic water.     

Effect of watershed parameters on mercury distribution in different environmental compartments in the Mobile Alabama River Basin, USA

Total mercury (THg) and mono-methylmercury (MeHg) levels in water, sediment, and largemouth bass (LMB) (Micropterus salmoides) were investigated at 52 sites draining contrasting land use/land cover and habitat types within the Mobile Alabama River Basin (MARB). Aqueous THg was positively associated with iron-rich suspended particles and highest in catchments impacted by agriculture. Sediment THg was positively associated with sediment organic mater and iron content, with the highest levels observed in smaller catchments influenced by wetlands, followed by those impacted by agriculture or mixed forest, agriculture, and wetlands. The lowest sediment THg levels were observed in main river channels, except for reaches impacted by coal mining. Sediment MeHg levels were a positive function of sediment THg and organic matter and aqueous nutrient levels. The highest levels occurred in agricultural catchments and those impacted by elevated sulfate levels associated with coal mining. Aqueous MeHg concentrations in main river channels were as high as those in smaller catchments impacted by agriculture or wetlands, suggesting these areas were sources to rivers. Elevated Hg levels in some LMB were observed across all types of land use and land cover, but factors such as shallow water depth, larger wetland catchment surface area, low aqueous potassium levels, and higher Chl a concentrations were associated with higher Hg burdens, particularly in the Coastal Plain province. It is suggested that the observed large variability in LMB Hg burdens is linked to fish displacement by anglers, differences in food web structure, and sediment biogeochemistry, with surficial sediment iron oxides buffering the flux of MeHg from sediments to deeper water pelagic food webs.     

Accumulation of mercury in the tissues of the common octopus Octopus vulgaris (L.) in two localities on the Portuguese coast

Mercury concentrations were measured in tissues of 12 individuals of Octopus vulgaris, captured by the commercial fishery at two points along the Portuguese coast, Viana do Castelo and Cascais, in spring 2002. Concentrations were determined in six tissues (digestive gland, branchial hearts, gills, mantle, arms, and gonads). Correlations between mercury concentrations in different tissues were examined as were correlations between mercury levels and total length, mantle length, weight, gonadosomatic index, digestive gland index, and state of maturation. Differences between sexes and localities were analysed. The concentration of mercury in the digestive gland (Viana, 0.58+/-0.08, and Cascais, 3.43+/-2.57 mg/kg dry weight) was higher than in the other tissues, and values were generally similar to those recorded in previous studies on octopods. Arm muscle contained most of the mercury with 56% of the total body burden followed by the digestive gland with 31%, mantle with 11%, gills with 0.8%, gonad with 0.5%, and branchial heart with 0.2%. In all tissues, mercury concentrations were slightly higher in samples from Cascais than in Viana do Castelo, which is consistent with higher concentrations recorded in seawater at Cascais. Levels of mercury determined in octopus were within the range of values legally defined as safe for human consumption.     

Bioaccumulation of mercury in benthic communities of a river ecosystem affected by mercury mining

The presence of mercury in the river Idrijca (Slovenia) is mainly due to 500 years of mercury mining in this region. In order to understand the cycling of mercury in the Idrijca ecosystem it is crucial to investigate the role of biota. This study is part of an ongoing investigation of mercury biogeochemistry in the river Idrijca, focusing on the accumulation and speciation of mercury in the lower levels of the food chain, namely filamentous algae, periphyton and macroinvertebrates. Mercury analysis and speciation in the biota and in water were performed during the spring, summer and autumn seasons at four locations on the river, representing different degrees of mercury contamination. Total (THg) and methyl mercury (MeHg) were measured. The results showed that the highest THg concentrations in biota correlate well with THg levels in sediments and water. The level of MeHg is spatially and seasonally variable, showing higher values at the most contaminated sites during the summer and autumn periods. The percentage of Hg as MeHg increases with the trophic level from water (0.1-0.8%), algae (0.5-1.3%), periphyton (1.6-8.8%) to macroinvertebrates (0.1-100%), which indicates active transformation, accumulation and magnification of mercury in the benthic organism of this heavily contaminated torrential river.     

Mercury empirical relationships in sediments from three Ontario lakes

Total mercury (THg), methyl mercury (MeHg), total organic carbon (TOC), sediment bulk density (SBD), redox potential (Eh) and percent fines measurements were made on sediment cores collected along transects from littoral to profundal depths in Harp, Dickie, and Blue Chalk lake located on the Canadian Shield near Dorset, Ontario, Canada to determine whether empirical relationships exist among these sediment properties.MeHg was positively correlated with THg in all sediments with a MeHg:THg ratio (0.004 ± 0.004) comparable to other uncontaminated profundal lakes. MeHg, MeHg:THg and TOC decreased with sediment depth within the core for all lakes, whereas THg only showed a decrease in Harp Lake. MeHg:THg ratio in surficial sediments was positively correlated with Eh and negatively correlated with TOC [MeHg:THg = − 0.009 ? TOC (%) + 0.001 ? Eh (mV) − 1.902, p = 0.026]; whereas THg was positively correlated with TOC [log THg (ppb) = 0.026 ? TOC (%) + 1.400, p < 0.0001].     

Total mercury and methylmercury in high altitude surface snow from the French Alps

Surface snow samples were collected weekly from the 31st of December 2008 to the 21st of June 2009 from Lake Bramant in the French Alps. Total mercury (THg), total dissolved mercury (THgD), methylmercury (MeHg) and particle distributions in surface snow were analyzed. Results showed that THg concentrations, MeHg concentrations and particle load increased with snow surface temperature, which is an indicator of rising temperatures as the season progresses. Significant correlations between MeHg and snow surface temperature and MeHg and total particles greater than 10 μm were observed. This suggests that the MeHg found in the snow originates from atmospheric deposition processes rather than in situ snowpack sources. This study suggests that an important post-winter atmospheric deposition of MeHg and THg occurs on summital zones of the French Alps and it is likely that this contamination originates from the surrounding valleys.     

Total arsenic, lead, cadmium, copper, and zinc in some salt rivers in the northern Andes of Antofagasta, Chile

Lake Velenje is located in one of the most polluted regions in Slovenia, the Salek Valley. The major source of pollution in the valley is the coal-fired thermal power plant in Sostanj (STPP, capacity 775 MW). It has five separate units. All units have electrostatic precipitators for fly ash removal. Unit 4 also has installed a wet flue gas desulfurisation system (FGD system). Total mercury (THg) concentrations were measured in lignite, slag and ash samples from the STPP. In flue gas, different mercury species (THg, MeHg, Hg2+, Hg0) were determined separately for unit 4 and unit 5 which use different flue gas cleaning technology. Mercury and methyl mercury (MeHg) concentrations were also measured in lake water at different depths, in inflow water, outflow water, rain, snow and lake sediments in order to establish the influence of the power plant on the lake. Most mercury emitted from the power plant is in the elemental form. The ratio between oxidised and elemental Hg depends on the flue gas cleaning technology. Mass balance calculations have been performed for the STPP. The results show that the major sources of mercury in Lake Velenje are wet deposition and lake inflows. Total and MeHg concentrations in the water column are very low and can be compared to other non-contaminated freshwater lakes in the world.     

Trace element concentrations in the Pacific harbor seal (Phoca vitulina richardii) in central and northern California

To determine concentrations of trace elements (THg, MeHg, Se, and Pb) in tissues of the Pacific harbor seal (Phoca vitulina richardii), live (n=186) and dead seals (n=53) were sampled throughout central and northern California from March 2003 to January 2005. There were significant differences in THg concentrations in blood and hair based on age (p<0.001). Adult male harbor seals had greater THg concentrations in their hair than adult female harbor seals (p<0.003). THg concentrations in liver increased linearly with age and delta15N (p<0.001); whereas, MeHg concentrations in liver increased exponentially until approximately 5 years of age with an asymptote at 1.3 microg/g wet weight. MeHg expressed as a percentage of THg (%MeHg) was best described by a decay function (r2=0.796, p<0.001), decreasing to a minimum at 4 years of age. Hepatic Se increased with age and was in equimolar ratios with THg in adults; whereas, molar ratio of Se:THg in pups deviated from a 1:1 ratio. Significant differences among study locations in THg concentrations in blood and hair were not detected. Assessing the possible effect of sampling location on Hg concentrations, however, was confounded and limited by lack of equal sample sizes for basic age and sex cohorts, a common dilemma in pinniped research.     

Total and methyl mercury transformations and mass loadings within a wastewater treatment plant and the impact of the effluent discharge to an alkaline hypereutrophic lake

Concerns over the fate and bioaccumulation of mercury (Hg) inputs to Onondaga Lake, a hypereutrophic lake in central New York, prompted an investigation into the concentrations and fluxes of Hg discharge from the Onondaga County Metropolitan Wastewater Treatment Plant (METRO WWTP). Discharge of methyl Hg (MeHg) is of concern because it is the form of Hg that readily bioaccumulates along the aquatic food chain. This study incorporated clean protocols for sampling and Hg analysis to evaluate: seasonal patterns in the concentrations of total Hg (THg) and MeHg in the WWTP unit processes; the production of MeHg within the unit processes of the WWTP; the overall fate of THg and MeHg within the WWTP; and the relative impact of the Hg discharged from the WWTP to Onondaga Lake. Concentrations of THg (range: 80-860 ng/L) and MeHg (0.7-17 ng/L) in raw sewage were highly variable, with higher concentrations observed in the summer months. The dynamics of THg though the WWTP were correlated with total suspended solids (TSS). As a result, the majority of the THg removal (55%) occurred during primary treatment. Overall, about 92% of the THg entering the plant was removed as sludge, with volatilization likely a minor component of the overall Hg budget. The transformation of MeHg through the plant differed from THg in that MeHg was not correlated with TSS, and displayed strong seasonal differences between winter (November to April) and summer (May-October) months. During the summer months, substantial net methylation occurred in the activated sludge secondary treatment, resulting in higher MeHg concentrations in secondary effluent. Net demethylation was the dominant mechanism during tertiary treatment, resulting in removal of substantial MeHg from the secondary effluent. The overall MeHg removal efficiency through the plant was about 70% with more efficient removal during summer months. Sediment trap collections made below the epilimnion of Onondaga Lake indicated average deposition rates of 12 μg/m²-day for THg and 0.33 μg/m²-day for MeHg. These deposition rates are more than an order of magnitude higher than the thermocline area normalized external loads from METRO effluent (0.85 μg/m²-day for THg, 0.05 μg/m²-day for MeHg). Our findings indicate that the impact of the discharge from METRO is relatively small, contributing about 10-15% of Hg to the total gross Hg input to the hypolimnion of the lake.     

Mercury distribution in a polluted marine area, ratio of total mercury, methyl mercury and selenium in sediments, mussels and fish

Total mercury, methyl mercury and selenium concentrations were determined in sediments and organisms from the Kaštela bay in the Central Adriatic, polluted with inorganic mercury by a chlor-alkali plant. Sediments and mussels (Mytilus galloprovincialis) contained high total mercury concentrations, especially in the vicinity of the source of pollution. The percentage of mercury in the methyl form increased from surface sediments (up to 1.37%) to the edible parts of mussels (0.1–27%, negatively correlated with total mercury concentrations) and to the fish, in which methyl mercury accounted for most of the mercury in the muscle tissue.     

Mercury concentrations in muscle, brain and bone of Western Alaskan waterfowl

Total mercury (THg), which includes both inorganic (Hg(2+)) and methylmercury (MeHg) species, has been reported for seabirds in the North Pacific and Alaska. For the Yup'ik and Aleut people of Alaska, waterfowl are a small but important seasonal component of the diet, but many Alaskan species have not been studied extensively for the presence of mercury. Birds are good subjects for examination of mercury concentrations because they feed at different trophic levels, they can be long-lived, and many are both abundant and widely distributed. In this study, we present the levels of mercury in muscle, brain, and bone tissue of 140 birds taken by subsistence food users across Western Alaska. THg wet weight mean concentrations in the 18 species of waterfowl surveyed ranged from 0.8 to 268.6 ng/g in muscle, from 0.4 to 197.7 ng/g in brain and from 0.7 to 422.9 ng/g in bone. The null hypothesis that there are no interspecific differences in the level of total mercury in the 18 species of Alaska birds surveyed was not supported. We found interspecific differences with the Lesser Scaup (Aythya affinis), and the Black Scoter (Melanitta nigra), having the highest muscle tissue levels of THg. In general, THg mean levels were higher in muscle than in brain with the exceptions of the Bar-tailed Godwit and Northern Shoveler. Bone THg were highest in the Black Scoter. The mean values for THg in the species studied are unlikely to cause adverse reproductive or behavioral effects in the birds.     

The variations of mercury in sediment profiles from a historically mercury-contaminated reservoir, Guizhou province, China

Baihua Reservoir in Guizhou Province, China, experienced serious Hg contamination from Guizhou Organic Chemical Plant (GOCP) between 1971 and 1997. However, the biogeochemical cycling of Hg in this reservoir is not well studied. Sediment cores were collected in fall 2002, spring 2003 and in spring and fall 2004. THg and MeHg concentrations in all sediment profiles ranged from 0.26 to 38.9 mg/kg and from 0.5 to 27.5 μg/kg (d.w.), respectively. The distribution of THg in sediment cores was characterized by a few peaks, which may correspond to the Hg-containing wastewater discharge history of the GOCP. The average THg concentrations in sediments cores decreased from upstream to downstream due to the deposition of particulate Hg, which is the major form of Hg in water. THg and MeHg concentrations in pore water varied from 6.1 to 5860 ng/L and from 0.3 to 15.4 ng/L, respectively, which were significantly higher than levels in the overlying water column. Average diffusive flux from sediment to water is 1642 and 36 ng/m²/day for THg and MeHg. The spatial distribution of THg in pore water from upstream to downstream showed the same trend as the sediment, but MeHg in pore water did not show a declining pattern with distance from the GOCP. These results suggested that sediments experienced serious contamination of Hg, and the contaminated sediment is an important Hg contamination source to the overlying water.     

Mercury and methylmercury concentrations in high altitude lakes and fish (Arctic charr) from the French Alps related to watershed characteristics

Total mercury (THg) and methylmercury (MeHg) concentrations were measured in the muscle of Arctic charr (Salvelinus alpinus) and in the water column of 4 lakes that are located in the French Alps. Watershed characteristics were determined (6 coverage classes) for each lake in order to evaluate the influence of watershed composition on mercury and methylmercury concentrations in fish muscle and in the water column. THg and MeHg concentrations in surface water were relatively low and similar among lakes and watershed characteristics play a major role in determining water column Hg and MeHg levels. THg muscle concentrations for fish with either a standardized length of 220 mm, a standardized age of 5 years or for individualuals did not exceed the 0.5 mg kg^− 1 fish consumption advisory limit established for Hg by the World Health Organization (WHO, 1990). These relatively low THg concentrations can be explained by watershed characteristics, which lead to short Hg residence time in the water column, and also by the short trophic chain that is characteristic of mountain lakes. Growth rate did not seem to influence THg concentrations in fish muscles of these lakes and we observed no relationship between fish Hg concentrations and altitude. This study shows that in the French Alps, high altitude lakes have relatively low THg and MeHg concentrations in both the water column and in Arctic charr populations. Therefore, Hg does not appear to present a danger for local populations and the fishermen of these lakes.     

Mercury in the Mackenzie River delta and estuary: Concentrations and fluxes during open-water conditions

Estimates of mercury (Hg) loadings to the Arctic Ocean from circumpolar rivers have not considered biogeochemical changes that occur when river water is temporarily stored in large deltas (delta effect). There are also few data describing Hg changes across the freshwater-saltwater transition zone (FSTZ) of these rivers. We assessed temporal changes in unfiltered total mercury (THg) and methylmercury (MeHg) concentrations during open-water 2004 in the Mackenzie River upstream of the Mackenzie River delta, and in 6 floodplain lakes across an elevation gradient. These data were used to calculate Hg fluxes from the Mackenzie River and to evaluate a delta effect on Hg using an estimate of delta river water storage and a mixing analysis. Mean THg concentrations were highest in river water (9.17 ± 5.51 ng/L) and decreased up the lake elevation gradient. Mean MeHg concentrations were highest in lakes periodically connected to the river (0.213 ± 0.122 ng/L) and MeHg concentrations in elevated lakes showed a mid-summer peak. Results from the mixing analysis showed that the delta effect may be large enough to affect Hg loadings to the Arctic Ocean. THg concentrations exiting the delta (10.2 ng/L) were 16% lower than those entering (12.1 ng/L), whereas MeHg showed little change. We calculated 2.5-month (open-water) THg and MeHg fluxes from the Mackenzie River of 1208 and 8.4 kg. These fluxes are similar in magnitude to previous annual estimates in the arctic literature suggesting that previously published annual Hg fluxes from the Mackenzie River may be large underestimates. We also assessed changes in Mackenzie River water THg and MeHg concentrations as it crossed the FSTZ during an open-water cruise. THg decreased non-conservatively across the estuary from 3.8-0.6 ng/L, possibly due to mixing and particle settling. MeHg concentrations were variable and near detection. Our results show that the Mackenzie River estuary is a dynamic environment and may have important controls on Hg delivered to the Arctic Ocean.     

Distributions of total mercury and methylmercury in surface sediments and fishes in Lake Shihwa, Korea

The concentrations of total mercury (THg) and methylmercury (MeHg) in the sediments of Lake Shihwa, an artificial salt lake in Korea located near two large industrial complexes, were determined to investigate the state of Hg contamination in the lake sediments and the effect of local Hg source. THg and MeHg concentrations in the sediments, monitored for 2 years, ranged from 0.02 to 0.28 µg g^− 1 and ≤ 0.026 to 0.67 ng g^− 1, respectively. The overall distribution of Hg in lake sediments showed higher values near industrial complexes and in the central part of the lake. However, the correlations between Hg and environmental factors, such as organic material (OM) content, and acid volatile sulfide (AVS), were weak and did not clearly explain the variation in Hg distribution. The spatial distribution of sediment Hg and monthly precipitation data during the sampling period showed that the amount of runoff following rain events and water gate operation may be additional important factors regulating Hg level and distribution in lake sediments. The levels of THg in fish species in this lake ranged from 9.8 to 35 ng g^− 1, suggesting that the bioavailability of sediment Hg in the lake may be low. Although the THg concentrations in Lake Shihwa sediment were lower than those in other foreign study sites, they were higher than in neighboring coastal regions, and are constantly increasing. This result indicates that the nearby industrial complexes may be the major source of Hg found in the sediments of Lake Shihwa.