Elevated Mercury Concentrations Research Articles

Exceptionally high levels of total mercury in deep-sea sharks of the Southeastern Mediterranean sea over the last ∼ 40 years

Deep-sea habitats are currently recognized as a hot spot for mercury (Hg) accumulation from anthropogenic sources, resulting in elevated concentrations of total mercury (THg) in deep-sea megafauna. Among them, deep-sea sharks (Class Chondrichthyes) are characterized by high trophic position and extended longevity and are, therefore, at high risk for mercury contamination. Despite this, sharks are overexploited by fishing activity in increasingly deeper water, worldwide, imposing health risks to human consumption. While it is imperative to better understand long-term mercury contamination in deep-sea megafauna, few historical data sets exist to capture this process. Here we explore four decades (1985–2022) of THg accumulation in five species of deep-sea sharks (G. melastomus, E. spinax, S. rostratus, C. granulosus, and D. licha) of the ultra-oligotrophic Southeastern Mediterranean Sea (SEMS) sampled during 19 research cruises. We exhibited exceptionally high THg levels (per length/weight), the highest as 16.6 μg g−1 (wet wt.), almost entirely (98.9 %; n = 298 specimens) exceeding the limit for safe consumption (0.3–0.5 μg THg g−1 wet wt.). The maximal THg levels of the long-lived species D. licha and C. granulosus in the SEMS were enriched by a factor of ∼ 7 and >10 compared to counterpart species from other oceanic areas, respectively. We attribute this to the ultra-oligotrophic conditions of the SEMS, which cause slower growth rates and dwarfism in deep-sea sharks, resulting in an extended exposure time to mercury contamination. In the long-lived species, C. granulosus and D. licha, a temporal increase of average THg levels of ∼ 80 % was recorded between 1987–1999 and 2021–2022. This likely reflects the long-term accumulation of historical anthropogenic Hg in deep-sea environments, which is further amplified in marginal seas such as the Mediterranean, impacted by global air pollution crossroads and surrounded by land-based pollution sources. Future consumption of products from deep-sea sharks is potentially high risk to human health.

Trophic magnification of Hg, PBDE and PCB in population of European perch with varying feeding ecology in the Baltic Sea

Marine ecosystems face a significant ecological challenge due to the introduction and cycling of hazardous substances. The recent stabilization of concentrations of specific hazardous substances, which were previously decreasing, indicates significant ongoing processes within the ecosystem. These processes continue to make these substances available within the food chain, even following the implementation of restrictions and the elimination of known anthropogenic sources. The present study investigated the transfer of mercury, PBDEs, PCBs and their congeners via trophic transfer by combining consumer dietary characteristics and concentrations of these pollutants using European perch (Perca fluviatilis) and its prey as model organisms.The elevated concentrations of mercury and the accelerated trophic magnification in the perch population at one of the sampling sites appear to be linked to the selective consumption of Decapoda. However, the frequency of occurrence of any particular prey item in the perch diet does not account for the declining magnification slopes of PCBs at the site. Furthermore, in the distant sampling sites, PCBs and PBDEs do not exhibit consistent trophic magnification slopes. This suggests the significance of pollution loads in the neighboring water bodies and the migration patterns of the assessed species.

Evaluation of Geology and Hydrochemistry of Nawfia-Agulu Axis of Anambra State, Southeastern Nigeria

The investigation of the geological, hydrochemical, and engineering characteristics of the Nawfia – Agulu area was carried out. The study aimed at mapping the geology through field data collection, outcrop logging, and laboratory analysis. Consequently, eleven soil and ten water samples were collected and analyzed through particle size distribution test; Atterberg limits tests and hydrochemical analysis to provide insights into the lithology, sediment characteristics, and water quality. The results indicated the dominance of the Ameki/Nanka Formation and Imo Formation as the underlying geology of the study area. The grain sizes of the sand samples ranged from medium to coarse grained, moderately to poorly sorted, and strongly positive to positively-skewed. The depositional environment was nearshore/beach, influenced by nearshore waves and turbulent currents. Engineering properties highlighted the prevalence of uniformly to well-graded soil and moderately to highly plastic behavior, as indicated by the mean plasticity index (PI) value of 26%. These findings suggest potential challenges for infrastructural development in some parts of the area. The water quality indicated slightly acidic water. The physical parameters and the major ions were within the permissible limits of World Health Organization (WHO) and the Nigerian Standard for Drinking Water Quality (NSDWQ). However, elevated concentrations of heavy metals, including lead, chromium, mercury, iron, and cadmium, in water sources exceeded the respective permissible limits for drinking water indicating contamination/pollution. The dominant water type was Ca2+ – Mg2+– SO42- – Cl– and the dominant hydrochemical process was simple dissolution or mixing and ion-exchange.

High resolution visualisation of tiemannite microparticles, essential in the detoxification process of mercury in marine mammals

The North Sea is an ecologically rich habitat for marine wildlife which has also been impacted by industrial developments and anthropogenic emissions of contaminants such as mercury. Marine mammals are particularly susceptible to mercury exposure, due to their trophic position, long lifespan, and dependence on (increasingly contaminated) aquatic prey species. To mitigate impact, marine mammals can detoxify methylmercury by binding it to selenium-containing biomolecules, creating insoluble mercury selenide granules. Here, liver, kidney, muscle, and brain samples from an adult male bottlenose dolphin (Tursiops truncatus) with known elevated mercury concentrations were analysed through scanning electron microscopy (SEM). Tiemannite (HgSe) deposits were identified in all organs, ranging from 400 nm to 5 μm in diameter, with particle size being organ-dependent. Although reported in other studies, this is the first time that the three-dimensional nature of tiemannite is captured in marine mammal tissue.

Reductions in plasma and urine mercury concentrations following N,N′bis-(2-mercaptoethyl) isophthalamide (NBMI) therapy: a post hoc analysis of data from a randomized human clinical trial

Environmental mercury exposure possesses a significant risk to many human populations. At present there are no effective treatments for acute mercury toxicity. A new compound, N,N′bis-(2-mercaptoethyl) isophthalamide (NBMI), a lipophilic chelating agent was created to tightly/irreversibly bind mercury. A post hoc dose-dependent analysis of NBMI therapy was undertaken on data from a randomized controlled NBMI human treatment trial on 36 Ecuadorian gold miners with elevated urinary mercury concentrations. Study subjects were randomly assigned to receive 100 milligram (mg) NBMI/day, 300 mg NBMI/day, or placebo for 14 days. For each study subject daily mg NBMI dose/Kilogram (Kg) bodyweight were determined and plasma and urine mercury concentrations (micrograms (µg)/Liter (L)) on study day 1 (pre-NBMI treatment), 15 (after 14 days of NBMI treatment) and 45 (30 days after NBMI treatment) were correlated with NBMI dosing using the linear regression statistic in SAS. Regression revealed significant inverse correlations between increasing per mg NBMI/Kg bodyweight/day and reduced concentrations of urinary and plasma mercury on study day 15 (reduced by in urine = 18–20 µg/L and plasma = 2 µg/L) and study day 30 (reduced by in urine = 15–20 µg/L and plasma = 4 µg/L) and significant correlations between reductions in mercury concentrations in urine and plasma. Significant 30% reductions in urinary mercury concentrations per mg NBMI/Kg bodyweight/day administered for 14 days were observed. This study supports the dose-dependent ability of NBMI therapy to significantly reduce mercury concentrations, particularly in the urine, in an acutely mercury exposed human population. NBMI therapy should be evaluated in other mercury exposed populations.

Home-produced eggs: An important pathway of methylmercury exposure for residents in mercury mining areas, southwest China

In light of the documented elevated concentrations of total mercury (Hg) and methylmercury (MeHg) in poultry originating from Hg-contaminated sites, a knowledge gap persists regarding the levels of Hg found in home-produced eggs (HPEs) and the associated dietary exposure risks in regions affected by Hg mining. To address this knowledge gap, a comprehensive investigation was undertaken with the primary objectives of ascertaining the concentrations of THg and MeHg in HPEs and evaluating the potential hazards associated with the consumption of eggs from the Wanshan Hg mining area in Southwest China. The results showed that THg concentrations in HPEs varied within a range of 10.5–809 ng/g (with a geometric mean (GM) of 64.1 ± 2.7 ng/g), whereas MeHg levels spanned from 1.3 to 291 ng/g (GM, 23.1 ± 3.4 ng/g). Remarkably, in half of all eggs, as well as those collected from regions significantly impacted by mining activities, THg concentrations exceeded the permissible maximum allowable value for fresh eggs (50 ng/g). Consumption of these eggs resulted in increased exposure risks associated with THg and MeHg, with GM values ranging from 0.024 to 0.17 µg/kg BW/day and 0.0089–0.066 µg/kg BW/day, respectively. Notably, the most substantial daily dosage was observed among children aged 2–3 years. The study found that consuming HPEs could result in a significant IQ reduction of 34.0 points for the whole mining area in a year. These findings highlight the potential exposure risk, particularly concerning MeHg, stemming from the consumption of local HPEs by residents in mining areas, thereby warranting serious consideration within the framework of Hg exposure risk assessment in mining locales.

First mercury and stable isotope assessment from an unusual mass stranding of rough-toothed dolphins (Steno bredanensis) (Artiodactyla: Delphinidae) in Azuero peninsula, Pacific coast of Panama

Introduction: Small cetaceans are good bioindicators of environmental contamination; however, knowledge about their ecotoxicological status in Central America is scarce. In Panama, access to samples from wild populations to determine the ecotoxicological status of oceanic dolphins is limited; therefore, stranding events provide an alternative for obtaining samples. In April 2016, a rare mass stranding event occurred in the Azuero Peninsula (Pacific coast of Panama), where 60 rough-toothed dolphins (Steno bredanensis) stranded, including ten which died on the beach.
 Objective: To assess total mercury (THg) concentrations, and δ13C and δ15N stable isotope values in rough-toothed dolphins for the first time in this region.
 Methods: Nine skin samples were collected from adults, stored in 70 % ethanol, and posteriorly analyzed to determine THg concentrations and stable isotope values.
 Results: THg concentrations ranged from 4 764 to 18 689 ng g-1 dry weight (dw) (mean = 12 841; SD = 5 083 ng g-1 dw), δ13C values ranged between −16.8 and −15.2 ‰ (mean = −16.2; SD = 0.6 ‰), and δ15N values ranged between 14.3 and 15.9 ‰ (mean = 15.0; SD = 0.5 ‰).
 Conclusions: High THg concentrations reported for this species in the Azuero Peninsula are consistent with values reported for rough-toothed dolphins in other areas worldwide, such as the central-northern Rio de Janeiro State in Brazil and La Guajira in the Colombian Caribbean. Elevated mercury (Hg) concentrations may be related to the rough-toothed dolphin diet, which according to δ15N values found here, appears to be based mainly on high trophic level prey that bioaccumulate more Hg in their tissues compared to lower trophic level organisms. However, additional dietary studies would be required to support these findings. Continuing monitoring of traditional dietary analysis, as well as contamination levels in fish and dolphins, is necessary to understand the dolphins’ ecotoxicology in Panama.

Detection of heavy metals and VOCs in streambed sediment indicates anthropogenic impact on intermittent streams of the U.S. Virgin Islands

Global surges in industrialization and human development have resulted in environmental contamination. Streambed sediment contamination threatens ecological and human health due to groundwater leaching and downstream contaminant mobilization. This is especially true in the wider Caribbean region, where streambed sediment contamination is understudied. In the current study, we assessed human impact on intermittent streams by measuring heavy metals and volatile organic compounds (VOCs) in streambed sediment on St. Croix in the United States Virgin Islands (USVI), where intermittent streams receive limited conservation and research attention. In contrast to our hypothesis that streambed sediment pollutant concentrations would be higher in developed, compared to undeveloped areas, contaminant concentrations did not vary significantly according to land cover. Elevated lead, mercury, and zinc concentrations were correlated with commercial building density, suggesting an unnatural origin of these elements in streambed sediment. At some sites, levels of arsenic, cadmium, chromium, nickel, lead, thallium, or zinc exceeded regulatory limits. The most prevalent VOCs at both developed and undeveloped sites were benzene and toluene. Sub-groups of heavy metals identified by principal component analysis indicated potential pollution sources, including fuel combustion (chromium, nickel, arsenic, selenium), vehicle exhaust, oil refining, and gasoline leaks (2-butanone and xylenes), and plastics (acetone and styrene). Our results suggest USVI intermittent streams require further research attention and intervention strategies for pollution reduction.

Variation in habitat use and its consequences for mercury exposure in two Eastern Ontario bat species, Myotis lucifugus and Eptesicus fuscus.

The St. Lawrence River in Eastern Ontario, Canada, has been a designated an area of concern due to past industrial contamination of sediment in some areas and transport of mercury from tributaries. Previous research using bats as sentinel species identified elevated concentrations of total mercury (THg) in fur of local bats and species-specific variation between little brown bats (Myotis lucifugus) and big brown bats (Eptesicus fuscus). Here, we investigated the mercury exposure pathways for these two species by testing the hypothesis that diet variation, particularly the reliance on aquatic over terrestrial insects, is a determinant of local bat mercury concentrations. We analyzed THg concentration and stable isotope ratios of δ15N and δ13C in fur of little and big brown bats, and in aquatic and terrestrial insects. Big brown bats, especially males, accumulated significantly higher THg concentrations in their fur compared to little brown bats. However, this difference was not related to diet because big brown bats consumed terrestrial insects, which were lower in mercury than aquatic insects, the primary prey for little brown bats. We also evaluated whether fur THg concentrations translate into molecular changes in tissues linked to (methyl)mercury toxicity by quantifying tissue changes in global DNA methylation and mitochondrial DNA abundance. No significant changes in DNA molecular markers were observed in relation to fur THg concentration, suggesting mercury exposure to local bats did not impact molecular level changes at the DNA level. Higher mercury in bats was not associated with local aquatic contamination or genotoxicity in this study area.

Mercury bioaccessiblity in freshwater fish species from northern Canada

Indigenous communities in northern Canada rely on locally harvested traditional foods, including fish, which provides them with nutritional, cultural, and social benefits. However, mercury exposure from fish consumption can pose a health risk for populations that consume large amounts of fish with elevated mercury concentrations. The bioaccessiblity of mercury in the tissue of northern Canadian freshwater fish is not yet known. To address this, samples from five commonly consumed freshwater fish species (Lake Trout, Northern Pike, Walleye, Lake Whitefish, and Burbot) caught from lakes in the Northwest Territories and Yukon, Canada were examined. Total mercury concentrations, fatty acid composition, and total mercury bioaccessibility differed significantly among fish species and lakes. Mean total mercury bioaccessibility using an in vitro gastrointestinal model ranged between 56 % and 96 % in muscle tissue across fish species and waterbodies examined and was 39 % in liver tissue from Burbot. Mean total mercury bioaccessibility was much lower (range: 38 % to 42 %) for a subset of samples run through only the gastric phase of the digestion model. Total mercury bioaccessibility was significantly lower (on average 40 % lower) in a subset of samples that were pan-fried in water. Thus, although cooking increased total mercury concentrations in pan-fried fish samples (likely due to moisture loss), bioaccessible concentrations of total mercury were lower (on average 32 % lower). Results from this study contribute to addressing a large knowledge gap in the literature regarding bioaccessibility of total mercury in northern freshwater fish species. To the best of our knowledge, this is the first study to examine mercury bioaccessibility in raw and cooked liver samples from freshwater fish. It also adds to the growing literature indicating that mercury bioaccessibility varies among fish species, locations, and cooking/preparation methods.

Distribution of Mercury in Drained Peatlands as the Effect of Secondary Transformation of Soil Organic Matter

Peat organic soils play a major role in the accumulation of soil organic matter (SOM) and the mercury (Hg) cycle. Large mercury resources in peatlands can be a source of methylmercury for many decades and centuries, even if deposition is significantly reduced. The organic matter of peatland soils drained for agricultural use is subject to secondary transformation, which may affect the accumulation and resources of mercury. The aim of our work is to assess the secondary transformation of organic matter in the soils of drained peatlands of the temperate climate zone and to examine whether it affects mercury resources and profile distribution in organic soils. Field research was conducted in peatlands located in eastern Poland. In the present study, evaluation of secondary transformations occurring after drainage was based on observations of soil morphological characteristics, physical and chemical properties as well as fractional composition of organic matter of the identified soil horizons (to depth 70 cm). Standard cold vapor atomic absorption spectrometry (CV-AAS) was used to measure the total mercury content. In our research, we found a significant effect of the secondary transformation of organic matter occurring in drained peatlands of the temperate climate zone on the total mercury content and stock in soils. The highest content and differentiation of mercury occurred in murshic horizons (up to a maximum depth of 43 cm). The average mercury content of the distinguished soil horizons is grouped in the following series (in μg kg−1): M1 (212.0) > M2 (182.8) > M3 (126.3) > Pt (84.9). The mercury stock, up to a depth of 70 cm in the tested soils, ranged from 17.5 to 39.6 mg m−2. As much as 82.2% of soil mercury was found in the upper murshic horizons. We found strong correlations between soil properties characteristically variable in the secondary transformation process and total mercury content. The increased content of humic substances in murshic horizons caused a significant increase in the total mercury content. Our research is of great importance for soil monitoring, as the amount of determined mercury was greatly influenced by the depth of sampling (up to 25 cm). The results of the research should be taken into account when planning the restoration of peatlands of the temperate climate zone. There is a potential risk that elevated mercury concentrations in the upper murshic horizons may be a source of methylmercury for a long period of time. In peat soils with a high concentration of mercury, the risk of contamination with this toxic metal should be determined before re-irrigation.

Biomarkers of seafood intake during pregnancy – Pollutants versus fatty acids and micronutrients

Intake of fish and seafood during pregnancy may have certain beneficial effects on fetal development, but measurement of intake using questionnaires is unreliable. Here, we assessed several candidate biomarkers of seafood intake, including long-chain omega 3 fatty acids (n-3 LCPUFA), selenium, iodine, methylmercury, and different arsenic compounds, in 549 pregnant women (gestational week 29) in the prospective birth cohort NICE (Nutritional impact on Immunological maturation during Childhood in relation to the Environment). Proportions of the fatty acids eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA) in erythrocytes were measured using gas chromatography with flame ionization detector. Selenium was measured in blood plasma and erythrocytes, mercury and arsenic in erythrocytes, and iodine and several arsenic compounds in urine, using inductively coupled plasma mass spectrometry, arsenic compounds after first being separated by ion exchange high-performance liquid chromatography (HPLC). Each biomarker was related to intake of total seafood and to intake of fatty and lean fish, and shellfish in third trimester, estimated from a semi-quantitative food frequency questionnaire filled out in gestational week 34. The pregnant women reported a median total seafood intake of 184 g/week (5th-95th percentiles: 34–465 g/week). This intake correlated most strongly with erythrocyte mercury concentrations (rho = 0.49, p < 0.001), consisting essentially of methylmercury, followed by total arsenic in erythrocytes (rho = 0.34, p < 0.001), and arsenobetaine in urine (rho = 0.33, p < 0.001), the main form of urinary arsenic. These biomarkers correlated well with intake of both fatty fish, lean fish, and shellfish. Erythrocyte DHA and plasma selenium correlated, although weakly, mainly with fatty fish (rho = 0.25 and 0.22, respectively, both p < 0.001). In conclusion, elevated concentrations of erythrocyte mercury and urinary arsenobetaine can be useful indicators of seafood intake, more so than the n-3 LCPUFAs. However, the relative importance of the biomarkers may differ depending on the type and amount of seafood consumed.

Mercury Contamination of Fish and Their Prey Across a Riverine Food Web

Lakes and reservoirs are frequently monitored by researchers for elevated mercury concentrations in sportfish. Rivers and streams, especially those of smaller orders, are less frequently monitored for mercury contamination and nonsport fishes and invertebrates, although important components of the food web, are rarely examined. We addressed this gap by surveying mercury levels in a stream community in the Kiamichi River in southeastern Oklahoma, U.S., by sampling fish and macroinvertebrates at ten sites in the river. We found elevated levels of mercury across taxa within the river including individuals of smallmouth bass populations 10–25 cm in length having concentrations (2986 ± 1053 ng/g dry weight) above the U.S. Environmental Protection Agency human limit. Furthermore, we observed high concentrations in darters and logperch (1133 ± 464 ng/g dry weight), nonsport fishes found predominantly in rivers and streams. Our results indicate mercury contamination can reach elevated concentrations in rivers and stream food webs, posing risks to both humans and wildlife.

Elevated Mercury Concentrations and Isotope Signatures (N, C, Hg) in Yellowfin Tuna (Thunnus albacares) from the Galápagos Marine Reserve and Waters off Ecuador

We examined how dietary factors recorded by C and N influence Hg uptake in 347 individuals of yellowfin tuna (Thunnus albacares), an important subsistence resource from the Galápagos Marine Reserve (Ecuador) and the Ecuadorian mainland coast in 2015-2016. We found no differences in total Hg (THg) measured in red muscle between the two regions and no seasonal differences, likely due to the age of the fish and slow elimination rates of Hg. Our THg concentrations are comparable to those of other studies in the Pacific (0.20-9.60 mg/kg wet wt), but a subset of individuals exhibited the highest Hg concentrations yet reported in yellowfin tuna. Mercury isotope values differed between Δ199 Hg and δ202Hg in both regions (Δ199 Hg = 2.86 ± 0.04‰ vs. Δ199 Hg = 2.33 ± 0.07‰), likely related to shifting food webs and differing photochemical processing of Hg prior to entry into the food web. There were significantly lower values of both δ15 N and δ13 C in tuna from Galápagos Marine Reserve (δ15 N: 8.5-14.2‰, δ13 C: -18.5 to -16.1‰) compared with those from the Ecuadorian mainland coast (δ15 N: 8.3-14.4‰, δ13 C: -19.4 to -11.9‰), of which δ13 C values suggest spatially constrained movements of tuna. Results from the pooled analysis, without considering region, indicated that variations in δ13 C and δ15 N values tracked changes of Hg stable isotopes. Our data indicate that the individual tuna we used were resident fish of each region and were heavily influenced by upwellings related to the eastern Pacific oxygen minimum zone and the Humboldt Current System. The isotopes C, N, and Hg reflect foraging behavior mainly on epipelagic prey in shallow waters and that food web shifts drive Hg variations between these populations of tuna. Environ Toxicol Chem 2022;41:2732-2744. © 2022 SETAC.

Factors related to fish mercury concentrations in Iowa lakes.

Mercury contamination in aquatic ecosystems is a global concern due to the health risks of consuming contaminated fishes. Fish mercury concentrations are influenced by a range of biotic and abiotic factors that vary among regions, but these complex interactions are difficult to disentangle. We collected bluegill (Lepomis macrochirus), white and black crappie (Pomoxis annularis; P. nigromaculatus), largemouth bass (Micropterus salmoides), walleye (Sander vitreus), muskellunge (Esox masquinongy), and northern pike (E. lucius) from waterbodies throughout Iowa and analyzed them for mercury concentrations. We used land use, water chemistry, and fish characteristics to explain variation in mercury concentrations among and within systems. Mercury concentrations were generally low and undetectable (< 0.05mg/kg) in 43% of fish analyzed. Detected mercury concentrations were highest in largemouth bass, muskellunge, northern pike, and walleye, lowest in black and white crappie and bluegill, and positively related to fish length and age. Mean lake depth, pH, watershed area to lake area ratio, and percent of watershed as open water were positively related to fish mercury concentrations whereas lake area and percent of watershed as agriculture, developed, forested, and grassland were negatively related to mercury concentrations. Additionally, mercury concentrations were higher in shallow natural lakes compared to other lake types. Our results indicate fish mercury concentrations are lower in Iowa lakes compared to other regions. Models we developed in this study can be used to identify other waterbodies that may have elevated mercury concentrations that can guide fish mercury monitoring programs.

Widespread elevated concentrations of gaseous elemental mercury in Guanajuato, Mexico, centuries after historical silver refining by mercury amalgamation

Silver (Ag) production in Hispanic America between the 16th and 19th centuries is thought to be one of the largest sources of anthropogenic mercury (Hg) emissions in history. Recent reviews of the chemistry behind the patio process, which used Hg amalgamation to extract Ag from ore, reveal that a large amount of the Hg may not have been immediately released to the atmosphere; instead, it may have been captured in the form of calomel (Hg2Cl2, in which Hg exists as monovalent HgI) and remained in the local environment. Here we show that Hg used in the patio process centuries ago in the Guanajuato Mining District of Mexico continues to elevate present-day concentrations of gaseous elemental mercury (GEM) throughout the region. In the ground-level air, GEM ranged from 8 to 454 ng m−3, exceeding the Northern Hemispheric average (~1.4 ng m−3) by up to two orders of magnitude. Much higher concentrations, up to 44,700 ng m−3, were found in the interstitial air of reprocessed mineral wastes, sediment, and soil. These highly elevated present-day GEM values are due, at least in part, to the disproportionation of legacy calomel, as supported by the presence of HgI in the reprocessed wastes and by the GEM release pattern from calomel disproportionation. Our results imply that the contribution of historical Ag refining to atmospheric Hg emissions must be re-evaluated to account for calomel and its subsequent disproportionation and releases of GEM to the present-day.

Decreasing mercury levels in consumer fish over the three decades of increasing mercury emissions in China

Fish consumption is the primary dietary route of human exposure to methylmercury. It has been well documented that elevated mercury concentration in fish in North America and Europe is linked to anthropogenic mercury emissions. China is the world’s largest producer, consumer, and emitter of mercury, as well as the world’s largest commercial fish producer and consumer. Although mercury pollution in fish in China is currently receiving much attention worldwide, its status remains largely unknown. Here, we conducted a meta-analysis on total mercury concentrations in marine and freshwater fish samples, covering 35,464 samples collected in China over the past 30 years. It is found that, opposite to the increasing emission and documented mercury contamination events, mercury levels in fish have gradually decreased in China over the past 30 years. The results were in sharp contrast to those found in North America and Europe. The mercury concentrations in fish were significantly anticorrelated with the fish catch and fish aquaculture and were inverse to trophic levels. Overfishing and the short lifecycle of aquaculture fish, both reducing the trophic level and the duration of mercury accumulation, were the most likely causes leading to the decline of mercury concentrations found in fish in China.

Elevated mercury and PCB concentrations in Dolly Varden (Salvelinus malma) collected near a formerly used defense site on Sivuqaq, Alaska

Environmental pollution causes adverse health effects in many organisms and contributes to health disparities for Arctic communities that depend on subsistence foods, including the Yupik residents of Sivuqaq (St. Lawrence Island), Alaska. Sivuqaq's proximity to Russia made it a strategic location for U.S. military defense sites during the Cold War. Two radar surveillance stations were installed on Sivuqaq, including at the Northeast Cape. High levels of persistent organic pollutants and toxic metals continue to leach from the Northeast Cape formerly used defense (FUD) site despite remediation efforts. We quantified total mercury (Hg) and polychlorinated biphenyl (PCB) concentrations, and carbon and nitrogen stable isotope signatures, in skin and muscle samples from Dolly Varden (Salvelinus malma), an important subsistence species. We found that Hg and PCB concentrations significantly differed across locations, with the highest concentrations found in fish collected near the FUD site. We found that 89% of fish collected from near the FUD site had Hg concentrations that exceeded the U.S. Environmental Protection Agency's (EPA) unlimited Hg-contaminated fish consumption screening level for subsistence fishers (0.049 μg/g). All fish sampled near the FUD site exceeded the EPA's PCB guidelines for cancer risk for unrestricted human consumption (0.0015 μg/g ww). Both Hg and PCB concentrations had a significant negative correlation with δ13C when sites receiving input from the FUD site were included in the analysis, but these relationships were insignificant when input sites were excluded. δ15N had a significant negative correlation with Hg concentration, but not with PCB concentration. These results suggest that the Northeast Cape FUD site remains a point source of Hg and PCB pollution and contributes to higher concentrations in resident fish, including subsistence species. Moreover, elevated Hg and PCB levels in fish near the FUD site may pose a health risk for Sivuqaq residents.

Efficient mercury sequestration from wastewaters using palm kernel and coconut shell derived biochars

Elevated mercury (Hg) concentrations in water bodies caused by illegal artisanal gold mining in Ghana is a serious health concern given the toxicity of Hg. As an ecofriendly cost-effective solution for removing Hg from these water bodies, we synthesized biochars using palm kernel (PB) and coconut shells (CB), which are dominant biomass wastes in Ghana. The biochars were sulfurized (SPB, SCB) and fabricated into polysulfone-based beads for Hg(II) sorption. The Hg(II) concentration, contact time, sorbent mass, and solution pH were investigated and were found to be influential on the sorption of Hg(II) from aqueous solution. The sulfurized biochars showed a faster Hg(II) removal (within 1h) compared to the pristine biochars. Sorption tests conducted using natural riverine water samples confirmed the potential use of the biochars, with SPB and SCB showing higher efficiencies than pristine PB and CB. The fabricated beads exhibited 70–90% efficiency in Hg(II) removal from 1.0 mg L−1 Hg solution and the sorption capacity was below 0.1 mg g−1, which we attribute to the mass of biochar used for the beads. The Hg(II) sorption mechanisms of PB and CB from spectroscopic analyses suggest that the biochars synthesized in this study can be used to treat Hg polluted waters and suitable for large-scale applications in natural water bodies.

Evidence that Pacific tuna mercury levels are driven by marine methylmercury production and anthropogenic inputs

Pacific Ocean tuna is among the most-consumed seafood products but contains relatively high levels of the neurotoxin methylmercury. Limited observations suggest tuna mercury levels vary in space and time, yet the drivers are not well understood. Here, we map mercury concentrations in skipjack tuna across the Pacific Ocean and build generalized additive models to quantify the anthropogenic, ecological, and biogeochemical drivers. Skipjack mercury levels display a fivefold spatial gradient, with maximum concentrations in the northwest near Asia, intermediate values in the east, and the lowest levels in the west, southwest, and central Pacific. Large spatial differences can be explained by the depth of the seawater methylmercury peak near low-oxygen zones, leading to enhanced tuna mercury concentrations in regions where oxygen depletion is shallow. Despite this natural biogeochemical control, the mercury hotspot in tuna caught near Asia is explained by elevated atmospheric mercury concentrations and/or mercury river inputs to the coastal shelf. While we cannot ignore the legacy mercury contribution from other regions to the Pacific Ocean (e.g., North America and Europe), our results suggest that recent anthropogenic mercury release, which is currently largest in Asia, contributes directly to present-day human mercury exposure.