Elevated Mercury Concentrations Research Articles

Dietary Advice on Inuit Traditional Food Use Needs to Balance Benefits and Risks of Mercury, Selenium, and n3 Fatty Acids

Elevated concentrations of mercury (Hg) are commonly found in the traditional foods, including fish and marine mammals, of Inuit living in Canada's Arctic. As a result, Inuit often have higher dietary Hg intake and elevated Hg blood concentrations. However, these same traditional foods are excellent sources of essential nutrients. The goals of this study were 1) to identify the traditional food sources of Hg exposure for Inuit, 2) to estimate the percentage of Inuit who meet specific nutrient Dietary Reference Intakes and/or exceed the Toxicological Reference Values (TRVs), and 3) to evaluate options that maximize nutrient intake while minimizing contaminant exposure. A participatory cross-sectional survey was designed in consultation with Inuit in 3 Canadian Arctic jurisdictions (Nunatsiavut, Nunavut, and the Inuvialuit Settlement Region). Estimated intakes for EPA (20:5n3) and DHA (22:6n3) met suggested dietary targets, and estimated selenium (Se) intake fell within the Acceptable Range of Oral Intake. Estimated intakes of Hg (rs = 0.41, P < 0.001), Se (rs = 0.44, P < 0.001), EPA (rs = 0.32, P < 0.001), and DHA (rs = 0.28, P < 0.001) were correlated with their respective blood concentrations. Mean estimated Hg intake (7.9 μg · kg−1 · wk−1) exceeded the TRV of 5.0 μg · kg−1 · wk−1, with 35% of the population above this guideline. Because the estimated intakes of each of the nutrients were strongly correlated (Se: rs = 0.92, P < 0.001; EPA: rs = 0.82, P < 0.001; DHA: rs = 0.81, P < 0.001) with estimated Hg intake, efforts to decrease Hg exposure must emphasize the overall healthfulness of traditional foods and be designed to prevent concomitant harm to the nutrient intakes of Inuit.

Comparison of laser induced breakdown spectroscopy and spark induced breakdown spectroscopy for determination of mercury in soils

Mercury is a toxic element found throughout the environment. Elevated concentrations of mercury in soils are quite hazardous to plants growing in these soils and also the runoff of soils to nearby water bodies contaminates the water, endangering the flora and fauna of that region. This makes continuous monitoring of mercury very essential. This work compares two potential spectroscopic methods (laser induced breakdown spectroscopy (LIBS) and spark induced breakdown spectroscopy (SIBS)) at their optimum experimental conditions for mercury monitoring. For LIBS, pellets were prepared from soil samples of known concentration for generating a calibration curve while for SIBS, soil samples of known concentration were used in the powder form. The limits of detection (LODs) of Hg in soil were calculated from the Hg calibration curves. The LOD for mercury in soil calculated using LIBS and SIBS is 483ppm and 20ppm, respectively. The detection range for LIBS and SIBS is discussed.

Forestry Influence by Stump Harvest and Site Preparation on Methylmercury, Total Mercury and Other Stream Water Chemistry Parameters Across a Boreal Landscape

Forestry has been reported to cause elevated mercury (Hg) concentrations in runoff water. However, the degree to which forestry operations influence Hg in runoff varies among sites. A synoptic study, covering 54 catchments distributed all over Sweden, subjected to either stump harvest (SH), site preparation (SP) or no treatment (Ref), was undertaken to reveal the degree of forestry impact and causes of eventual variation. All streams were sampled twice, in autumn 2009 and summer 2010. There were no significant differences in total mercury (THg) and methylmercury (MeHg) concentrations between the three treatments in either 2009 or 2010. However, when pooling the treated catchments (that is, SH and SP) and taking catchment properties such as latitude into account, the treatment had a significant influence on the THg and MeHg concentrations. Although the treatment effect on THg and MeHg did not differ between SH and SP, the study did reveal significant forestry effects on potassium (K) and total nitrogen (TN) that were greater in the SH catchments and lower in the SP catchments. Partial least square (PLS) regressions indicated that organic matter was the most important variable influencing both the THg and MeHg concentrations. There were no significant differences between the treatment groups when comparing the ratios of THg/total organic carbon (TOC) and MeHg/TOC, suggesting that the high concentrations of THg and MeHg observed at some of the treated catchments are associated with increased concentrations of TOC rather than new methylation or increased mobilization caused by factors other than TOC.

Mining, Metallurgy and the Historical Origin of Mercury Pollution in Lakes and Watercourses in Central Sweden

In Central Sweden an estimated 80% of the lakes contain fish exceeding health guidelines for mercury. This area overlaps extensively with the Bergslagen ore region, where intensive mining of iron ores and massive sulfide ores occurred over the past millennium. Although only a few mines still operate today, thousands of mineral occurrences and mining sites are documented in the region. Here, we present data on long-term mercury pollution in 16 sediment records from 15 lakes, which indicate that direct release of mercury to lakes and watercourses was already significant prior to industrialization (<AD 1800). Thirteen of our lakes show increases in mercury from 3-fold-equivalent to the enrichment factor in many remote lakes today-to as much as 60-fold already during the period AD 1500-1800, with the highest values in the three lakes most closely connected to major mines. Although the timing and magnitude of the historical increases in mercury are heterogeneous among lakes, the data provide unambiguous evidence for an incidental release of mercury along with other mining metals to lakes and watercourses, which suggests that the present-day problem of elevated mercury concentrations in the Bergslagen region can trace its roots back to historical mining.

Mercury Stable Isotopes in Seabird Eggs Reflect a Gradient from Terrestrial Geogenic to Oceanic Mercury Reservoirs

Elevated mercury concentrations ([Hg]) were found in Alaskan murre (Uria spp.) eggs from the coastal embayment of Norton Sound relative to insular colonies in the northern Bering Sea-Bering Strait region. Stable isotopes of Hg, carbon, and nitrogen were measured in the eggs to investigate the source of this enrichment. Lower δ(13)C values in Norton Sound eggs (-23.3‰ to -20.0‰) relative to eggs from more oceanic colonies (-20.9‰ to -18.7‰) indicated that a significant terrestrial carbon source was associated with the elevated [Hg] in Norton Sound, implicating the Yukon River and smaller Seward Peninsula watersheds as the likely Hg source. The increasing [Hg] gradient extending inshore was accompanied by strong decreasing gradients of δ(202)Hg and Δ(199)Hg in eggs, indicating lower degrees of mass-dependent (MDF) and mass-independent Hg fractionation (MIF) (respectively) in the Norton Sound food web. Negative or zero MDF and MIF signatures are typical of geological Hg sources, which suggests murres in Norton Sound integrated Hg from a more recent geological origin that has experienced a relatively limited extent of aquatic fractionation relative to more oceanic colonies. The association of low δ(202)Hg and Δ(199)Hg with elevated [Hg] and terrestrial δ(13)C values suggested that Hg stable isotopes in murre eggs effectively differentiated terrestrial/geogenic Hg sources from oceanic reservoirs.

Seafood Consumption and Blood Mercury Concentrations in Jamaican Children With and Without Autism Spectrum Disorders

Mercury is a toxic metal shown to have harmful effects on human health. Several studies have reported high blood mercury concentrations as a risk factor for autism spectrum disorders (ASDs), while other studies have reported no such association. The goal of this study was to investigate the association between blood mercury concentrations in children and ASDs. Moreover, we investigated the role of seafood consumption in relation to blood mercury concentrations in Jamaican children. Based on data for 65 sex- and age-matched pairs (2-8years), we used a General Linear Model to test whether there is an association between blood mercury concentrations and ASDs. After controlling for the child's frequency of seafood consumption, maternal age, and parental education, we did not find a significant difference (P=0.61) between blood mercury concentrations and ASDs. However, in both cases and control groups, children who ate certain types of seafood (i.e., salt water fish, sardine, or mackerel fish) had significantly higher (all P<0.05) geometric means blood mercury concentration which were about 3.5 times that of children living in the US or Canada. Our findings also indicate that Jamaican children with parents who both had education up to high school are at a higher risk of exposure to mercury compared to children with at least one parent who had education beyond high school. Based on our findings, we recommend additional education to Jamaican parents regarding potential hazards of elevated blood mercury concentrations, and its association with seafood consumption and type of seafood.

Elevated Mercury Concentrations in Humans of Madre de Dios, Peru

The enormous increase in practically unregulated mining in Madre de Dios Peru is leading to massive release of liquid elemental mercury to the environment. Rapidly increasing global prices for gold are causing a massive upsurge in artisanal mining in the Peruvian Amazon, considered to be one of the most biodiverse places on the planet. This study identifies the current levels of mercury in the human population, through identifying levels of total mercury in human hair in mining zones of Madre de Dios Department and in the nearby city of Puerto Maldonado. A regression analysis reveals that fish consumption, gender, and location of residence were significant indicators of mercury levels; while duration of residence and age had no significant relationship to mercury levels. Increased fish consumption levels were the strongest indicators of increased total mercury levels across the entire population. The levels of total mercury in hair was significantly (α = 0.05) higher in mining zones, than Puerto Maldonado. In both areas men had significantly higher levels than women, likely due to a difference in metabolism or varying levels of direct involvement in gold mining- a male predominated industry. This is the first study to show the health threat that mercury poses to this region, however further research needs to be done to gain a more refined understanding of the predominant routes of exposure in this population.

The fate of mercury in Arctic terrestrial and aquatic ecosystems, a review

Environmental contextMercury, in its methylated form, is a neurotoxin that biomagnifies in marine and terrestrial foodwebs leading to elevated levels in fish and fish-eating mammals worldwide, including at numerous Arctic locations. Elevated mercury concentrations in Arctic country foods present a significant exposure risk to Arctic people. We present a detailed review of the fate of mercury in Arctic terrestrial and marine ecosystems, taking into account the extreme seasonality of Arctic ecosystems and the unique processes associated with sea ice and Arctic hydrology. AbstractThis review is the result of a series of multidisciplinary meetings organised by the Arctic Monitoring and Assessment Programme as part of their 2011 Assessment ‘Mercury in the Arctic’. This paper presents the state-of-the-art knowledge on the environmental fate of mercury following its entry into the Arctic by oceanic, atmospheric and terrestrial pathways. Our focus is on the movement, transformation and bioaccumulation of Hg in aquatic (marine and fresh water) and terrestrial ecosystems. The processes most relevant to biological Hg uptake and the potential risk associated with Hg exposure in wildlife are emphasised. We present discussions of the chemical transformations of newly deposited or transported Hg in marine, fresh water and terrestrial environments and of the movement of Hg from air, soil and water environmental compartments into food webs. Methylation, a key process controlling the fate of Hg in most ecosystems, and the role of trophic processes in controlling Hg in higher order animals are also included. Case studies on Eastern Beaufort Sea beluga (Delphinapterus leucas) and landlocked Arctic char (Salvelinus alpinus) are presented as examples of the relationship between ecosystem trophic processes and biologic Hg levels. We examine whether atmospheric mercury depletion events (AMDEs) contribute to increased Hg levels in Arctic biota and provide information on the links between organic carbon and Hg speciation, dynamics and bioavailability. Long-term sequestration of Hg into non-biological archives is also addressed. The review concludes by identifying major knowledge gaps in our understanding, including: (1) the rates of Hg entry into marine and terrestrial ecosystems and the rates of inorganic and MeHg uptake by Arctic microbial and algal communities; (2) the bioavailable fraction of AMDE-related Hg and its rate of accumulation by biota and (3) the fresh water and marine MeHg cycle in the Arctic, especially the marine MeHg cycle.

Blood mercury levels among fish consumers residing in areas with high environmental burden

Mercury is a ubiquitous, persistent toxicant found in the environment. In water, mercury bioaccumulates up the food chain and leads to high concentrations in fish. Consumption of contaminated fish is the major source of exposure to mercury in the US. The objective of this study was to enroll persons living in areas selected by the Environmental Protection Agency (EPA) to have high mercury concentrations and who consume at least 6oz of locally caught fish per week to determine the feasibility of monitoring future trends among a population identified as highly exposed. Blood samples were collected at time of interview and analyzed for mercury. Participants (n=287) were enrolled from North Carolina, Maryland, and South Dakota. Participants reported eating an average of five servings of fish per week. The overall geometric mean for total mercury was 0.75μgL−1, with North Carolina having the highest mean level (2.02μgL−1). Overall, 42% of the study population had levels greater than the US geometric mean 0.83μgL−1. The number of servings of fish consumed was not found to be associated with blood mercury levels. We were able to identify some persons with elevated mercury concentrations living in areas identified by EPA; however, identifying and monitoring a highly exposed population over time would be challenging.

Environmental geochemistry studies in the area of Idrija mercury mine, Slovenia

Five centuries of mining and processing of mercury ore in the Idrija area have resulted in widespread contamination of different environmental compartments. Environmental impacts on a regional and local scale, caused by atmospheric emissions from the Idrija ore roasting plant, were established in the investigations of mercury spatial distribution in soil and attic dust in 160 km(2) area. Very high values were determined in the Idrijca River valley, and they decrease exponentially with the distance from Idrija. Mercury concentrations in attic dust are higher than in surrounding soils and the attic dust/soil ratio changes with distance. Measurements of mercury in the air confirmed widespread dispersion of mercury and showed highly elevated mercury concentrations around roasting plant and mine ventilation shaft. Beside, systematic monitoring of mercury contents in the stream sediments has demonstrated that huge amounts of mercury are stored in areas where ancient overbank sediments were deposited, and there was no decrease in mercury concentration in active sediments during the last 15 years. Recently, interesting and extremely polluted locations of historical small-scale roasting sites in the Idrija surroundings were discovered. Ongoing geochemical study aims to determine the extreme pollution and significance of these sites for wider contamination of soils and aquatic systems. Presented studies have shown that Hg mining in Idrija caused intense pollution of local and regional environment including the aquatic systems in the Gulf of Trieste, which is seen as the final sink of a major part of the Hg stored in soils and river sediments in the Idrija area.

Why are hatching and emergence success low? Mercury and selenium concentrations in nesting leatherback sea turtles (Dermochelys coriacea) and their young in Florida

Leatherback sea turtles (Dermochelys coriacea) have low hatching and emergence success compared to other sea turtle species. Postmortem examinations of hatchlings showed degeneration of heart and skeletal muscle that was similar to that found in other neonates with selenium deficient mothers. Selenium deficiency can result from elevated concentrations of bodily mercury. Ingested mercury is detoxified by the liver through mercury–selenium compound formation. In animals persistently exposed to mercury, the liver’s ability to detoxify this element may decrease, especially if dietary selenium is insufficient. We measured mercury and selenium concentrations in nesting female leatherbacks and their hatchlings from Florida and compared the levels to hatching and emergence success. Both liver selenium and the liver selenium-to-mercury ratio positively correlated with leatherback hatching and emergence success. This study provides the first evidence for the roles of mercury and selenium in explaining low reproductive success in a globally imperiled species, the leatherback sea turtle.

The tropical African mercury anomaly: Lower than expected mercury concentrations in fish and human hair

Mercury is a neurotoxin and global pollutant, and wetlands and newly flooded areas are known to be sites of enhanced production of monomethylmercury, the form of mercury that is readily biomagnified in aquatic food chains to potentially toxic levels. The Okavango Delta in Botswana, Southern Africa, is the largest inland delta in the world and a wetland ecosystem that experiences dramatic annual flooding of large tracts of seasonal floodplains. The Delta was, therefore, expected to be home to high mercury levels in fish and to be an area where local subsistence fishing communities would be at substantial risk of mercury toxicity from fish consumption. Total mercury concentrations measured in 27 species of fish from the Okavango Delta averaged (mean ± s.d., wet weight) 19 ± 19 ng g −1 in non-piscivorous fish, and 59 ± 53 ng g −1 in piscivorous fish. These mercury concentrations are similar to those reported for fish from lakes in other areas of tropical Africa, demonstrating that not all wetlands are sites of elevated mercury concentrations in biota. Even more intriguing is that concentrations of mercury in fish from across tropical Africa are systematically and substantially lower than those typically reported for fish from freshwater ecosystems elsewhere globally. The reasons for this apparent “African mercury anomaly” are unclear, but this finding poses a unique opportunity to improve our understanding of mercury's biogeochemical cycling in the environment. Mercury concentrations measured in human hair collected in subsistence fishing communities in the Okavango Delta were similarly low (0.21 ± 0.22 μg g −1 dry weight) despite high levels of fish consumption, and reflect the low mercury concentrations in the fish here.

Use of biogenic and abiotic elemental selenium nanospheres to sequester elemental mercury released from mercury contaminated museum specimens

Mercuric chloride solutions have historically been used as pesticides to prevent bacterial, fungal and insect degradation of herbarium specimens. The University of Manchester museum herbarium contains over a million specimens from numerous collections, many preserved using HgCl 2 and its transformation to H g v 0 represents a health risk to herbarium staff. Elevated mercury concentrations in work areas (∼1.7 μg m −3) are below advised safe levels (<25 μg m −3) but up to 90 μg m −3 mercury vapour was measured in specimen boxes, representing a risk when accessing the samples. Mercury vapour release correlated strongly with temperature. Mercury salts were observed on botanical specimens at concentrations up to 2.85 wt% (bulk); XPS, SEM–EDS and XANES suggest the presence of residual HgCl 2 as well as cubic HgS and HgO. Bacterially derived, amorphous nanospheres of elemental selenium effectively sequestered the mercury vapour in the specimen boxes (up to 19 wt%), and analysis demonstrated that the H g v 0 was oxidised by the selenium to form stable HgSe on the surface of the nanospheres. Biogenic Se 0 can be used to reduce H g v 0 in long term, slow release environments.

Potential impact of rainfall on the air-surface exchange of total gaseous mercury from two common urban ground surfaces

Abstract The impact of rainfall on total gaseous mercury (TGM) flux from pavement and street dirt surfaces was investigated in an effort to determine the influence of wet weather events on mercury transport in urban watersheds. Street dirt and pavement are common urban ground surfaces that concentrate many substances (eroded soil, leaf and vegetation litter, automobile debris, industrial atmospheric fallout) which can contain elevated mercury concentrations. In this study, the primary analyses included (i) observing the time series flux of TGM from pavement and street dirt following surface wetting and (ii) determining if wet deposition provides a fresh source of mercury that is available for release (emission) when applied to these surfaces. Application of de-ionized water (DI) and rainwater both induced an immediate 65% increase in TGM emission from pavement (from 0.5 to 1.4 ng m−2 h−1 [based on averages]). For street dirt, an immediate 70% increase in emission was induced following DI water application (from 3.0 to 9.0 ng m−2 h−1 [based on averages]) and an immediate 30% increase in emission following rainwater application (from 4.5 to 6.5 ng m−2 h−1 [based on averages]). Both surfaces showed continuous elevated release of TGM following the initial water application stage. There was a decrease in emission as the pavement surface dried. Despite the difference in immediate TGM emission from street dirt using both solutions, statistical evaluation indicated there was no prolonged difference. This suggests that mercury in rainwater was not available for re-emission when applied to these surfaces, at least for the time frame studied (2 h after water application). Therefore, it is likely that the elevated TGM emission following water application resulted primarily from pre-existing mercury. Removal of pre-existing mercury by water application followed a zero order process for both surfaces; however, removal rates were much different for each surface (k = 0.26 ng m−2 min−1 for street dirt; k = 0.03 ng m−2 min−1 for pavement). Results from laboratory surface washing experiments revealed only 0.1% of all available surface-bound mercury on pavement was removed by surface emission 90 min after a simulated light rainfall event (0.13 cm of rainfall).

Rapid Monitoring of Mercury in Air from an Organic Chemical Factory in China Using a Portable Mercury Analyzer

A chemical factory, using a production technology of acetaldehyde with mercury catalysis, was located southeast of Qingzhen City in Guizhou Province, China. Previous research showed heavy mercury pollution through an extensive downstream area. A current investigation of the mercury distribution in ambient air, soils, and plants suggests that mobile mercury species in soils created elevated mercury concentrations in ambient air and vegetation. Mercury concentrations of up to 600 ng/m3 in air over the contaminated area provided evidence of the mercury transformation to volatile Hg(0). Mercury analysis of soil and plant samples demonstrated that the mercury concentrations in soil with vaporized and plant-absorbable forms were higher in the southern area, which was closer to the factory. Our results suggest that air monitoring using a portable mercury analyzer can be a convenient and useful method for the rapid detection and mapping of mercury pollution in advanced field surveys.

Influence of Physiochemical and Watershed Characteristics on Mercury Concentration in Walleye, Sander vitreus, M.

Elevated mercury concentration has been documented in a variety of fish and is a growing concern for human consumption. Here, we explore the influence of physiochemical and watershed attributes on mercury concentration in walleye (Sander vitreus, M.) from natural, glacial lakes in South Dakota. Regression analysis showed that water quality attributes were poor predictors of walleye mercury concentration (R² = 0.57, p = 0.13). In contrast, models based on watershed features (e.g., lake level changes, watershed slope, agricultural land, wetlands) and local habitat features (i.e., substrate composition, maximum lake depth) explained 81% (p = 0.001) and 80% (p = 0.002) of the variation in walleye mercury concentration. Using an information theoretic approach we evaluated hypotheses related to water quality, physical habitat and watershed features. The best model explaining variation in walleye mercury concentration included local habitat features (W(i) = 0.991). These results show that physical habitat and watershed features were better predictors of walleye mercury concentration than water chemistry in glacial lakes of the Northern Great Plains.

The Effect of Contaminated Prey on Feeding, Activity, and Growth of Young-of-the-Year Bluefish, Pomatomus saltatrix, in the Laboratory

Young-of-the-year (YOY) bluefish, Pomatomus saltatrix, reside in some contaminated estuaries of the mid-Atlantic bight during their early life history, and as a result of this exposure, they may bioaccumulate high levels of contaminants, including polychlorinated biphenyls (PCBs), pesticides, and methyl mercury. Young-of-the-year bluefish from the Tuckerton, NJ, area of Great Bay (TK) were fed daily in a laboratory with common prey fish, menhaden, and mummichog from two sites: TK (reference) or Hackensack River (HR) (contaminated). Bluefish fed HR prey and the HR prey themselves had significantly elevated concentrations of PCBs, pesticides, and total mercury compared to TK counterparts. The bluefish fed contaminated prey for 4 months displayed significantly reduced feeding, spontaneous activity, and growth compared to the bluefish fed TK prey. Alterations of bluefish behavior and growth from exposure to contaminants may have detrimental effects on migration, overwinter survival, and recruitment success.

Temporal and spatial trends of organochlorines and mercury in fishes from the St. Clair River/Lake St. Clair corridor, Canada

The temporal and spatial relationships of a suite of organochlorine contaminants and mercury were examined in various fish species of the St. Clair River/Lake St. Clair corridor, Canada, in order to evaluate the effectiveness of remediation efforts and to assess the risk to human and wildlife fish consumers. In Lake St. Clair, fish tissue concentrations of mercury, polychlorinated biphenyls (PCBs), octachlorostyrene (OCS), hexachlorobenzene (HCB), and dichlorodiphenyltrichloroethane (DDT) decreased consistently from the 1970s until the 1980s and 1990s, after which the rate of contaminant decline slowed or concentrations stabilized. This trend was consistent in up to 13 species (both young-of-the-year and adult fishes) comprising different trophic positions and dietary habits, suggesting that the changes were reflective of ambient conditions rather than food web processes. Elevated concentrations of mercury, PCBs, OCS, HCB, and DDT were detected in St. Clair River young-of-the-year spottail shiner compared with fish from Lake Huron, indicating that non-atmospheric inputs of these chemicals, likely originating from sediment, remain in the St. Clair River. Current concentrations of mercury and PCBs, and mercury, PCBs, and DDT remain of concern to human and wildlife fish consumers, respectively. Given that contaminant decreases have generally stabilized in fish, we suggest that further natural recovery of contaminants in St. Clair corridor fishes will be slow since contaminants will likely continue to be influenced by sediment levels.

Elevated Concentrations of Methyl Mercury in Streams after Forest Clear-Cut: A Consequence of Mobilization from Soil or New Methylation?

Concentrations of inorganic, mercuric mercury (Hg(II)), methyl mercury (MeHg) and ancillary chemistry measured in first-order streams draining 0-4 (N = 20) and 4-10 (N = 27) year-old clear-cuts of former Norway Spruce Picea abies (Karst.) forest stands were compared with concentrations in streams draining >70 year-old Norway Spruce reference stands (N = 10). Concentrations of MeHg, and ratios of MeHg TOC(-1) and Hg(II) TOC(-1), were significantly (p < 0.01) elevated in 0-4 year-old clear-cuts, as compared to references. The only ancillary variable showing a significant elevation for 0-4 year-old clear-cuts was Mn (p < 0.02). The 4-10 year-old clear-cuts showed intermediate concentrations with nonsignificant differences as compared to references. pH, nitrate, sulfate, Ca, Fe, TOC, TON, and the aromaticity of TOC (SUVA(254 nm)) showed nonsignificant differences between clear-cut age classes and references. Assuming that MeHg and Hg(II) are mobilized from soil to stream to a similar relative extent as a consequence of clear-cutting, a calculation showed that (1)/(6) of the elevated MeHg concentration was due to enhanced mobilization from soil and (5)/(6) was due to new methylation of Hg(II) 0-4 years after clear-cut. New methylation after clear-cut is suggested to be stimulated by an increased availability of electron donors for methylating bacteria, as a consequence of degradation of logging residue ("slash") and soil organic matter. A subdivision of sites situated above and below the highest postglacial coastline (HC) revealed a significant elevation of MeHg, MeHg TOC(-1) and Hg(II) TOC(-1) (p < 0.05) beyond their references in 0-4 year-old clear-cuts above (but not below) the HC. This suggests that postglacial deposits of FeS(s) and FeS(2)(s) were not an important factor for elevation of MeHg after clear-cut.

Activated carbon for mercury control: Implications for fly ash management

As more utilities begin to use activated carbon injection (ACI) for mercury control, the potential for the presence of elevated concentrations of mercury, other air toxic elements, and activated carbon to impact fly ash management needs to be evaluated. Several Energy & Environmental Research Center (EERC) projects have allowed the collection of comparative baseline fly ash samples and associated fly ash–activated carbon (AC) samples from full-scale demonstrations of ACI for mercury emission control. These samples were evaluated for mercury and air toxic element content and mobility and for performance criteria to facilitate a better understanding of the impact of these components to specific utilization applications, including use as a mineral admixture in concrete. These data are compared with published data from samples collected at similar large-scale mercury emission control tests. The data presented are in agreement with previous results from the EERC, the U.S. Environmental Protection Agency, and elsewhere that mercury associated with fly ash is stable and unlikely to be released under most management conditions. Additionally, this paper will discuss the potential for fly ash–AC samples to be used as a mineral admixture in concrete and other large-volume use applications.