重金属汞

Mercury (Hg) is a global contaminant affecting aquatic ecosystems' health. Chronic exposure to Hg has shown that the normal development of zebrafish embryo-larvae is affected. However, the molecular mechanisms behind the toxicity of Hg on fish embryonic development are still poorly understood. This work aimed to investigate the effects of Hg exposure on zebrafish embryo-larvae using a combined approach at individual (mortality, embryo development and locomotor behavior) and biochemical (neurotoxicity and oxidative stress enzymatic activities and protein phosphatase expression) levels. The Fish Embryo Toxicity assay followed the Organization for Economic Cooperation and Development Guideline 236 and used a concentration range between 13 and 401 μg Hg/L. Lethal and developmental endpoints were examined at 24, 48, 72 and 96 hpf. Biochemical markers, including Acetylcholinesterase (AChE), Catalase (CAT), Glutathione Reductase (GR), and Glutathione-S-Transferase (GST) activities and, for the first time, the expression of the protein phosphatase 1 gamma (PP1γ) was assessed after 24, 48, 72 and 96 h of exposure to 10 and 100 μg Hg/L. The behavioral effects of a sublethal range of Hg (from 0.8 to 13 μg Hg/L) were assessed using an automated video tracking system at 120 hpf. Several developmental abnormalities on zebrafish embryos and larvae, including pericardial edema, spin and tail deformities and reduced rate of consumption of the yolk sac, were found after exposure to Hg (LC50 at 96 hpf of 139 μg Hg/L) with EC50 values for total malformations ranging from 22 to 264 μg Hg/L. After 96 hpf, no significant effects were observed in the CAT and GR activities. However, an increase in the GST activity in a concentration and time-dependent manner was found, denoting possible stress-related adaptation of zebrafish embryos to deleterious effects of Hg exposure. The AchE activity showed a response pattern in line with the behavioral responses. At the lowest concentration tested, no significant effects were found for the AChE activity, whereas a decrease in AChE activity was observed at 100 μg Hg/L, suggesting that exposure to Hg induced neurotoxic effects in zebrafish embryos which in turn may explain the lack of equilibrium found in this study (EC50 at 96 hpf of 83 μg Hg/L). Moreover, a decrease in the PP1γ expression was found after 96 h of exposure to 10 and 100 μg Hg/L. Thus, we suggest that Hg may be an inhibitor of PP1γ in zebrafish embryos-larvae and thus, along with the alterations in the enzymatic activity of GST, explain some of the developmental malformations observed, as well as the lack of equilibrium. Hence, in this study, we propose the use of PP1 expression, in combination with apical and biochemical endpoints, as a precursor for assessing Hg's toxic mechanism on embryonic development.

Mercury or mercury (Hg) is a type of metal as an organic and inorganic compound that can be found in nature and is spread in rocks, ores, soil, water and air. Mercury in the body can be detected in biological materials such as urine, blood, breast milk and hair. This study aims to analyze the content and toxicity of mercury (Hg) in biological samples such as blood, hair, urine and breast milk with various analytical methods including CV-AAS, AAS, CV-AFS, ICP-MS, FI-CV-AAS, and Mercury Analyzers. Data collection was based on the Literature Review by collecting several published research journals both at national and international levels which were filtered according to inclusion and exclusion criteria using the PRISMA method (Preferred Reporting Item for Systematic Review and Meta-Analysis). The method used depends on the needs of the analysis, its sensitivity and availability. Of the several methods used, AAS or atomic absorption spectrophotometry is the most commonly used method, because this method is simple and considered fast for analyzing mercury levels in biological samples.

Here, we subjected the marine copepod Tigriopus japonicus to environmentally-relevant concentrations of microplastics (MPs) and mercury (Hg) for three generations (F0-F2) to investigate their physiological and molecular responses. Hg accumulation and phenotypic traits were measured in each generation, with multi-omics analysis conducted in F2. The results showed that MPs insignificantly impacted the copepod's development and reproduction, however, which were significantly compromised by Hg exposure. Interestingly, MPs significantly increased Hg accumulation and consequently aggravated this metal toxicity in T. japonicus, demonstrating their carrier role. Multi-omics analysis indicated that Hg pollution produced numerous toxic events, e.g., induction of apoptosis, damage to cell/organ morphogenesis, and disordered energy metabolism, ultimately resulting in retarded development and decreased fecundity. Importantly, MPs enhanced Hg toxicity mainly via increased oxidative apoptosis, compromised cell/organ morphogenesis, and energy depletion. Additionally, phosphoproteomic analysis revealed extensive regulation of the above processes, and also impaired neuron activity under combined MPs and Hg exposure. These alterations adversely affected development and reproduction of T. japonicus. Overall, our findings should offer novel molecular insights into the response of T. japonicus to long-term exposure to MPs and Hg, with a particular emphasis on the carrier role of MPs on Hg toxicity.

Due to human activities, high abundances of nano/microplastics (N/MPs) concurrent with metal pollution have become a serious problem in the global marine environment. Because of displaying a high surface-area-to-volume ratio, N/MPs can serve as the carriers of metals and thus increase their accumulation/toxicity in marine biota. As one of the most toxic metals, mercury (Hg) causes adverse effects on marine organisms but whether environmentally relevant N/MPs can play a vector role of this metal in marine biota, as well as their interaction, is poorly known. To evaluate the vector role of N/MPs in Hg toxicity, we first performed the adsorption kinetics and isotherms of N/MPs and Hg in seawater, as well as ingestion/egestion of N/MPs by marine copepod Tigriopus japonicus, and second, the copepod T. japonicus was exposed to polystyrene (PS) N/MPs (500-nm, 6-μm) and Hg in isolation, combined, and incubated forms at environmentally relevant concentrations for 48 h. Also, the physiological and defense performance including antioxidant response, detoxification/stress, energy metabolism, and development-related genes were assessed after exposure. The results indicated N/MPs significantly increased Hg accumulation and thus its toxicity effects in T. japonicus as exemplified by decreased transcription of genes related to development and energy metabolism and increased transcriptional levels of genes functioning in antioxidant and detoxification/stress defense. More importantly, NPs were superimposed onto MPs and produced the most vector effect in Hg toxicity to T. japonicus, especially in the incubated forms. Overall, this study highlighted the role of N/MPs as a potential risk factor for increasing the adverse effects of Hg pollution, and emphasized the adsorption forms of contaminants by N/MPs should doubly be considered in the continuing researches.

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Mercury (Hg) is a heavy metal (HM) that affects crop growth and productivity. In a previous study, we found that application of exogenous abscisic acid (ABA) alleviated growth inhibition in Hg-stressed wheat seedlings. However, the physiological and molecular mechanisms underlying ABA-mediated Hg detoxification remained unclear. In this study, Hg exposure reduced the plant fresh and dry weights and root numbers. Exogenous ABA treatment significantly resumed the plant growth, increased the plant height and weight, and enriched the roots numbers and biomass. The application of ABA enhanced Hg absorption and raised the Hg levels in the roots. In addition, exogenous ABA decreased Hg-induced oxidative damage and significantly brought down the activities of antioxidant enzymes, such as SOD, POD and CAT. Global gene expression patterns in the roots and leaves exposed to HgCl2 and ABA treatments were examined via RNA-Seq. The data showed that genes related to ABA-mediated Hg detoxification were enriched in functions related to cell wall formation. Weighted gene co-expression network analysis (WGCNA) further indicated that the genes implicated in Hg detoxification were related to cell wall synthesis. Under Hg stress, ABA significantly induced expression of the genes encoding cell wall synthesis enzymes, regulated the activity of hydrolase, and increased the concentrations of cellulose and hemicellulose, hence promoting cell wall synthesis. Taken together, these results suggest that exogenous ABA could alleviate Hg toxicity in wheat by promoting cell wall formation and suppressing translocation of Hg from roots to shoots.

The continuous fragmentation of plastics and release of synthetic nanoplastics from products have been aggravating nanoplastic pollution in the marine ecosystem. The carrier role of nanoplastics may increase the bioavailability and toxicity effects of toxic metals, e.g., mercury (Hg), which is of growing concern. Here, the copepod Tigriopus japonicus was exposed to polystyrene nanoplastics (PS NPs) and Hg (alone or combined) at environmental realistic concentrations for three generations (F0-F2). Then, Hg accumulation, physiological endpoints, and transcriptome were analyzed. The results showed that the copepod's reproduction was significantly inhibited under PS NPs or Hg exposure. The presence of PS NPs caused significantly higher Hg accumulation, lower survival, and lower offspring production in copepods relative to Hg exposure, suggesting an increased threat to the copepod's survivorship and health. From the molecular perspective, combined PS NPs and Hg caused a graver effect on the DNA replication, cell cycle, and reproduction pathways relative to Hg exposure, linking to lower levels of survivorship and reproduction. Taken together, this study provides an early warning of nanoplastic pollution for the marine ecosystem not only because of their adverse effect per se but also their carrier role for increasing Hg bioaccumulation and toxicity in copepods.

Growing evidence demonstrates that global change can modulate mercury (Hg) toxicity in marine organisms; however, the consensus on such effect is lacking. Here, we conducted a meta-analysis to evaluate the effects of global change stressors on Hg biotoxicity according to the IPCC projections (RCP 8.5) for 2100, including ocean acidification (-0.4 units), warming (+4 °C), and their combination (acidification-warming). The results indicated an overall aggravating effect (ln RRΔ = -0.219) of global change on Hg toxicity in marine organisms, while the effect varied with different stressors; namely, acidification potentially alleviates Hg biotoxicity (ln RRΔ = 0.117) while warming and acidification-warming have an aggravating effect (ln RRΔ = -0.328 and -0.097, respectively). Moreover, warming increases Hg toxicity in different trophic levels, i.e., primary producers (ln RRΔ = -0.198) < herbivores (ln RRΔ = -0.320) < carnivores (ln RRΔ = -0.379), implying increasing trends of Hg biomagnification through the food web. Notably, ocean hypoxia appears to boost Hg biotoxicity, although it was not considered in our meta-analysis because of the small sample size. Given the persistent global change and combined effects of these stressors in marine environments, multigeneration and multistressor research is urgently needed to fully disclose the impacts of global change on Hg pollution and its risk.

The growing use of plastics, including microplastics (MPs), has enhanced their potential release into aquatic environments, where microalgae represent the basis of food webs. Due to their physicochemical properties, MPs may act as carriers of organic and inorganic pollutants. The present study aimed to determine the toxicity of polyethylene MPs (plain and oxidized) and the model pollutants chlorpyrifos (CPF) and mercury (Hg) on the red microalgae Rhodomonas lens, to contribute to the understanding of the effects of MPs and associated pollutants on marine ecosystems, including the role of MPs as vectors of potentially harmful pollutants to marine food webs. R. lens cultures were exposed to MPs (1-1000 μg/L; 25-24,750 particles/mL), CPF (1-4900 μg/L), Hg (1-500 μg/L), and to CPF- and Hg-loaded MPs, for 96 h. Average specific growth rate (ASGR, day-1), cellular viability and pigment concentration (chlorophyll a, c2 and carotenoids) were measured at 48 and 96 h. No significant effects were observed on the growth pattern of the microalgae after 96-h exposure to plain and oxidized MPs. However, a significant increase in cell concentration was detected after 48-h exposure to plain MPs. A decrease of the ASGR was noticed after exposure to CPF, Hg and to CPF/Hg-loaded MPs, whereas viability was affected by exposure to MPs, CPF and Hg, alone and in combination. Chlorophyll a and c2 significantly decreased when microalgae were exposed to plain MPs and CPF, while both pigments significantly increased when exposed to CPF-loaded MPs. Similarly, chlorophyll and carotenoids content significantly decreased after exposure to Hg, whereas a significant increase in chlorophyll a was observed after 48-h exposure to Hg-loaded MPs, at the higher tested concentration. Overall, the presence of MPs modulates the toxicity of Hg and CPF to these microalgae, decreasing the toxic effects on R. lens, probably due to a lower bioavailability of the contaminants.

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The present study addresses existing data on the affinity and conjugation of sulfhydryl (thiol; -SH) groups of low- and high-molecular-weight biological ligands with mercury (Hg). The consequences of these interactions with special emphasis on pathways of Hg toxicity are highlighted. Cysteine (Cys) is considered the primary target of Hg, and link its sensitivity with thiol groups and cellular damage. In vivo, Hg complexes play a key role in Hg metabolism. Due to the increased affinity of Hg to SH groups in Cys residues, glutathione (GSH) is reactive. The geometry of Hg(II) glutathionates is less understood than that with Cys. Both Cys and GSH Hg-conjugates are important in Hg transport. The binding of Hg to Cys mediates multiple toxic effects of Hg, especially inhibitory effects on enzymes and other proteins that contain free Cys residues. In blood plasma, albumin is the main Hg-binding (Hg2+, CH3Hg+, C2H5Hg+, C6H5Hg+) protein. At the Cys34 residue, Hg2+ binds to albumin, whereas other metals likely are bound at the N-terminal site and multi-metal binding sites. In addition to albumin, Hg binds to multiple Cys-containing enzymes (including manganese-superoxide dismutase (Mn-SOD), arginase I, sorbitol dehydrogenase, and δ-aminolevulinate dehydratase, etc.) involved in multiple processes. The affinity of Hg for thiol groups may also underlie the pathways of Hg toxicity. In particular, Hg-SH may contribute to apoptosis modulation by interfering with Akt/CREB, Keap1/Nrf2, NF-κB, and mitochondrial pathways. Mercury-induced oxidative stress may ensue from Cys-Hg binding and inhibition of Mn-SOD (Cys196), thioredoxin reductase (TrxR) (Cys497) activity, as well as limiting GSH (GS-HgCH3) and Trx (Cys32, 35, 62, 65, 73) availability. Moreover, Hg-thiol interaction also is crucial in the neurotoxicity of Hg by modulating the cytoskeleton and neuronal receptors, to name a few. However, existing data on the role of Hg-SH binding in the Hg toxicity remains poorly defined. Therefore, more research is needed to understand better the role of Hg-thiol binding in the molecular pathways of Hg toxicology and the critical role of thiols to counteract negative effects of Hg overload.

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Mercury (Hg) is an environmental pollutant that threatens aquatic life. Many environmental factors, including water temperature, are reported to influence the toxicity of dissolved chemicals in the aquatic ecosystem. Therefore, we investigated the impact of thermal stress on Hg-induced subchronic toxicity in Nile tilapia (Oreochromis niloticus). Fish were randomly allocated into five groups. Group I served as the control and kept at 25 °C. Groups II, III, IV, and V were reared at 25, 28, 31, and 34 °C, respectively, and co-exposed to HgCl2 (1/10 LC50) for 42 days. Blood and tissue samples were collected after 21 and 42 days. All HgCl2-exposed groups exhibited significant elevations in serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea, and creatinine, along with decreases in the serum total protein and albumin. In addition, marked reductions in antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSPx), were observed. Remarkable increases in Hg tissue concentrations were detected along with increases in heat shock protein (HSP) 70 mRNA expression. Interestingly, the patterns data that were recorded were more coincident with the water temperature than the period of exposure. In conclusion, water temperature and exposure period are two crucial factors modulating HgCl2-induced toxicity and bioaccumulation in Nile tilapia. Our findings provide new insights concerning the impact of thermal stress as an environmental factor on Hg toxicity and bioaccumulation in Nile tilapia and, in turn, on fish and fish consumer health.

The present study reveals the effect of mercury (Hg) and sodium nitroprusside (SNP) on plant growth and metabolism in soybean cultivars (Pusa-24, Pusa-37and Pusa-40). Mercury stress decreased growth and biomass yield, and gas exchange attributes in all soybean cultivars. External supplementation of SNP mitigated Hg toxicity by improving growth and gas exchange parameters. Electrolyte leakage (EL) increased accompanied with elevated levels of malondialdehyde (MDA) and H2O2 under Hg stress, however, they were found to be reduced in all cultivars upon the exogenous application of SNP. The activities of anti-oxidative enzymes, superoxide dismutase and catalase (SOD and CAT) and those enzymes involved in the ascorbate-glutathione pathway were impaired by Hg stress, but they were regulated by the application of SNP. Accumulation of Hg and NO in the shoots and roots were also regulated by the application of NO. Although, all three cultivars were affected by Hg stress, Pusa-37 was relatively less affected. Mercury stress affected the growth and development of different soybean cultivars, but Pusa-37 being tolerant was less affected. Pusa-37 was found to be more responsive to SNP than Pusa-24, Pusa-40 under Hg toxicity. The external supplementation of SNP could be a sustainable approach to economically utilize Hg affected soils.

The heavy metals lead (Pb), cadmium (Cd) and mercury (Hg) are common environmental pollutants that can be detected simultaneously in blood, serum, and urine samples from the general human population. However, there is limited information regarding toxicity of low-level exposure to Pb, Cd, and Hg mixtures. Our previous research showed the interaction of these three elements at low concentrations in vitro. In this study, we further evaluate early effects of low dose exposure to Pb, Cd, and Hg mixtures on the brain, heart, liver, kidney, and testicle in rats. Pregnant rats were exposed to various concentrations of heavy metal mixtures (MM) in drinking water, during gestation and lactation, and the impacts on offspring were measured at postnatal day 23. Our results showed that the concentrations of Pb, Cd, and Hg in the blood of rat pups were similar to those in the blood of the general human population. Additionally, the MM concentrations in their blood and brain significantly increased in a dose-dependent manner. MM exposure caused histopathological changes in the brain, liver, kidney and testicle. Statistically significant increases in liver CYP450 and PON1, kidney KIM1, and decrease in testicle SDH were observed. In the brain, significant increases were detected in oxidative stress, intracellular free calcium, and cell apoptosis. Further neurobehavioral testing revealed that MM exposure caused dose-dependent impairments in learning and memory as well as sensory perception. MM exposure also disrupted synapse remodeling, which may be associated with pathways involved in dendritic spine growth, maintenance, and elimination. These results suggested that exposure to Pb, Cd, and Hg mixtures, at human environmental exposure related levels, caused damage to multiple organs as well as impairments in neurobehavioral functions of rats. Our findings emphasize the need to control and regulate potential sources of heavy metal contamination.

Mercury (Hg) is one of the most toxic heavy metals with strong negative effects on the plant growth and functions. Salicylic acid (SA) is an important signaling molecule which confers tolerance to metal toxicities but little is known about the mechanisms of SA-mediated alleviation of Hg stress. Here, physiochemical and molecular responses of Hg-stressed lemon balm (Melissa officinalis L.) to exogenous SA were investigated to reveal SA-induced tolerance mechanisms. The CHLG gene of lemon balm which encodes chlorophyll synthase was also partly isolated and sequenced for the first time. Hg stress markedly decreased growth, relative water content (RWC) and photosynthetic pigments of the plant. However, exogenous SA significantly mitigated the toxic effects of mercury on the growth and RWC and enabled plant to maintain chlorophylls to the similar levels of unstressed plants. Hg-induced oxidative damage was also reduced following treatment with SA and treated plants showed the lower extent of lipid peroxidation which was accompanied with the higher free proline and phenolics contents and elevation of the antioxidant capacity as evidenced by DPPH radical scavenging and FRAP assays. Moreover, SA treatment resulted in up-regulation of CHLG and phenylalanine ammonia-lyase (PAL) genes as key components of chlorophyll and phenylpropanoid routes, respectively. Our results collectively indicate the ameliorative effects of exogenous SA in mercury toxicity through coordinated alternations in plant metabolic processes which provide insights to better understand mechanisms of Hg tolerance in lemon balm plant.

Marine biota have been co-challenged with ocean warming and mercury (Hg) pollution over many generations because of human activities; however, the molecular mechanisms to explain their combined effects are not well understood. In this study, a marine planktonic copepod Pseudodiaptomus annandalei was acutely exposed to different temperature (22 and 25 °C) and Hg (0 and 118 μg/L) treatments in a 24-h cross-factored experiment. Hg accumulation and its subcellular fractions were determined in the copepods after exposure. The expression of the genes of superoxide dismutase (SOD), glutathione peroxidase (GPx), metallothionein1 (mt1), heat shock protein 70 (hsp70), hsp90, hexokinase (hk), and pyruvate kinase (pk) was also analyzed. Both the Hg treatment alone and the combined exposure of warmer temperature plus Hg pollution remarkably facilitated Hg bioaccumulation in the exposed copepods. Compared with the Hg treatment alone, the combined exposure increased total Hg accumulation and also the amount of Hg stored in the metal-sensitive fractions (MSF), suggesting elevated Hg toxicity in P. annandalei under a warmer environment, given that the MSF is directly related to metal toxicity. The warmer temperature significantly up-regulated the mRNA levels of mt1, hsp70, hsp90, and hk, indicating the copepods suffered from thermal stress. With exposure to Hg, the mRNA level of SOD increased strikingly but the transcript levels of hsp90, hk, and pk decreased significantly, indicating that Hg induced toxic events (e.g., oxidative damage and energy depletion). Particularly, in contrast to the Hg treatment alone, the combined exposure significantly down-regulated the mRNA levels of SOD and GPx but up-regulated the mRNA levels of mt1, hsp70, hsp90, hk, and pk. Collectively, the results of this study indicate that ocean warming will potentially boost Hg toxicity in the marine copepod P. annandalei, which is information that will increase the accuracy of the projections of marine ecosystem responses to the joint effects of climate change stressors and metal pollution on the future ocean.

This study provides information on mercury (Hg) localization, speciation and ligand environment in edible mushrooms: Boletus edulis, B. aereus and Scutiger pes-caprae collected at non-polluted and Hg polluted sites, by LA-ICP-MS, SR-μ-XRF and Hg L3-edge XANES and EXAFS. Mushrooms (especially young ones) collected at Hg polluted sites can contain more than 100 μg Hg g-1 of dry mass. Imaging of the element distribution shows that Hg accumulates mainly in the spore-forming part (hymenium) of the cap. Removal of hymenium before consumption can eliminate more than 50% of accumulated Hg. Mercury is mainly coordinated to di-thiols (43-82%), followed by di-selenols (13-35%) and tetra-thiols (12-20%). Mercury bioavailability, as determined by feeding the mushrooms to Spanish slugs (known metal bioindicators owing to accumulation of metals in their digestive gland), ranged from 4% (S. pes-caprae) to 30% (B. aereus), and decreased with increasing selenium (Se) levels in the mushrooms. Elevated Hg levels in mushrooms fed to the slugs induced toxic effects, but these effects were counteracted with increasing Se concentrations in the mushrooms, pointing to a protective role of Se against Hg toxicity through HgSe complexation. Nevertheless, consumption of the studied mushroom species from Hg polluted sites should be avoided.

The present study aimed to evaluate the protective role of Selenium (Se) (0.1 ppm) on the male reproductive system of the catfish Clarias gariepinus exposed to sublethal doses of Mercury (Hg) (0.04 and 0.12 ppm) for 30 days. Indicators of seminal and gonadal hormone disruption (testosterone, estradiol and 11 keto testosterone), antioxidants (total antioxidant capacity (TAO), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx)), oxidative stress biomarkers (lipid peroxidation (LPO), percentage of DNA fragmentation, carbonylated proteins (CP) and nitric oxide (NO)) and histopathological alterations in testicles of Clarias gariepinus were determined. The exposure to Hg resulted in a high accumulation of residues of this metal in testicular tissues. The results showed a significant decrease in sperm count, activity and motility and in all gonadal hormones in Hg exposed groups. Hg exposure also induced a decline in TAO, SOD, CAT and GPx, whereas LPO, DNA fragmentation, CP and NO significantly increased in testicles of C. gariepinus respect to the control group. Although exposure to Se did not reduce the degree of mercury bioconcentration in the testicles, the sperm quality parameters were recovered. Moreover, TAO levels and GPx activity significantly increased after fish exposure to Se, whereas CP levels decreased. LPO, NO, CAT and SOD were also partially normalized when compared with the groups exposed to only Hg. In conclusion, the results showed that Hg, even in the small doses is capable to induce reproductive toxicity in the male catfish. Se exposure partially restored the values of biochemical parameters and sperm quality in Hg-treated fish suggesting protective effects against Hg reproductive toxicity.

Simple Summary This investigation was executed to establish the threshold level of inorganic and organic mercury incorporated in the diet of juvenile olive flounder in relation to the broken-line regression model for the percentage of weight gain of fish. Organic mercury incorporated diet resulted in more toxic behavior than its counterpart inorganic mercury in olive flounder. Mercury was found to be more biomagnified in kidney tissue than liver and gill tissues of fish. The study has importance in terms of knowledge on mercury toxicity in marine fish. Abstract Mercury as one of the most toxic elements can be present in organic or inorganic form in marine fishes, which may cause a potential threat to public health. In this study, we investigated to determine the dietary organic (O-Hg) and inorganic (I-Hg) mercury threshold levels on induced mercury toxicity in juvenile olive flounder, Paralichthys olivaceus as a marine fish model. Twenty-eight fish averaging 3.1 ± 0.05 g (mean ± SD) were arbitrarily assigned to each of 27 tanks. Each tank was arbitrarily restricted to triplicates of nine experimental diets for eight weeks. The experimental diets were manufactured to contain 0 (Control), 10 (I-Hg10, O-Hg10), 20 (I-Hg20, O-Hg20), 40 (I-Hg40, O-Hg40) and 160 (I-Hg160, O-Hg160) mg/kg diet in organic form as methylmercury (MeHg) or in inorganic form as mercuric chloride (HgCl2). At the termination of the experimental trial, weight gains (WGs) of fish fed the control and 10 (I-Hg10, O-Hg10) diets were remarkably higher than those of fish fed the 20 (I-Hg20, O-Hg20), 40 (I-Hg40, O-Hg40) and 160 (I-Hg160, O-Hg160) (p < 0.05). Specific growth rate and feed efficiency of fish fed control and 10 (I-Hg10, O-Hg10) diets were significantly higher than those of fish fed 40 (I-Hg40, O-Hg40) and 160 (I-Hg160, O-Hg160) diets. In comparison to the dietary inorganic mercury, dietary MeHg bioaccumulation rates were significantly higher in the tissue levels according to the dietary inclusion levels. MeHg accumulated mostly in kidney, followed by liver and gill tissues. HgCl2 accumulated in tissues, in decreasing order, liver > kidney > gills. A broken-line regression model for percentage of WG indicated that the threshold toxicity level for an Hg-incorporated diet of juvenile olive flounder could be 13.5 mg Hg/kg in the form of HgCl2 and 8.7 mg Hg/kg in the form of MeHg.

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Aims: Lactobacillus strains have protective effects against heavy metals while relieving oxidative stress and modulating the immune response. Mechanisms that ameliorate heavy metal toxicity and the relationship between probiotics and gut barrier protection in the process of heavy metal pathogenesis was poorly understood. Methods and Results: In this study, Lactobacillus brevis 23017 (LAB, L. brevis 23017), a selected probiotics strain with strong mercury binding capacities, was applied to evaluate the efficiency against mercury toxicity in a mouse model. Histopathological results along with HE stains show that L. brevis 23017 protects the integrity of the small intestinal villus, which slows weight loss in response to Hg exposure. The qRT-PCR results demonstrate that L. brevis 23017 maintains a normal mucosal barrier via modulation of tight junction proteins. Importantly, the present study demonstrates that L. brevis 23017 effectively ameliorates injury of the small intestine by reducing intestinal inflammation and alleviating oxidative stress in animal models. Moreover, L. brevis 23017 blocks oxidative stress and inflammation through MAPK and NF-κB pathways, as shown by western blot. Conclusions: Together, these results reveal that L. brevis 23017 may have applications in the prevention and treatment of oral Hg exposure with fermented functional foods by protecting gut health in daily life.

Contamination by mercury (Hg) is a worldwide concern because of Hg toxicity and biomagnification in aquatic food webs. Nevertheless, bioavailability and cellular toxicity pathways of inorganic (IHg) and methyl-Hg (MeHg) remain poorly understood. We analyzed the uptake, transcriptomic, and physiological responses in the microalga Chlamydomonas reinhardtii exposed to IHg or MeHg. Bioavailability of MeHg was up to 27× higher than for IHg. Genes involved in cell processes, energy metabolism and transport were dysregulated by both Hg species. Physiological analysis revealed an impact on photosynthesis and reduction–oxidation reaction metabolism. Nevertheless, MeHg dysregulated a larger number of genes and with a stronger fold-change than IHg at equivalent intracellular concentration. Analysis of the perturbations of the cell’s functions helped to derive a detailed mechanistic understanding of differences in cellular handling of IHg and MeHg resulting in MeHg having a stronger impact. This knowledge is central for the prediction of impact of toxicants on organisms.

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A number of observations indicate that heavy metals are able to alter cellular metabolic pathways through induction of a prooxidative state. Nevertheless, the outcome of heavy metal-mediated effects in the development of human diseases is debated and needs further insights. Cancer is a well-established DNA mutation-linked disease; however, epigenetic events are perhaps more important and harmful than genetic alterations. Unfortunately, we do not have reliable screening methods to assess/validate the epigenetic (promoter) effects of a physical or a chemical agent. We propose a mechanism of action whereby mercury acts as a possible promoter carcinogen. In the present contribution, we resume our previous studies on mercury tested at concentrations comparable with its occurrence as environmental pollutant. It is shown that Hg(II) elicits a prooxidative state in keratinocytes linked to inhibition of gap junction-mediated intercellular communication and proinflammatory cytokine production. These combined effects may on one hand isolate cells from tissue-specific homeostasis promoting their proliferation and on the other hand tamper the immune system defense/surveillance checkmating the whole organism. Since Hg(II) is not a mutagenic/genotoxic compound directly affecting gene expression, in a broader sense, mercury might be an example of an epigenetic tumor promoter or, further expanding this concept, a “metagenetic” effector.

Background The scientific discoveries of health risks resulting from methylmercury exposure began in 1865 describing ataxia, dysarthria, constriction of visual fields, impaired hearing, and sensory disturbance as symptoms of fatal methylmercury poisoning. Objective Our aim was to examine how knowledge and consensus on methylmercury toxicity have developed in order to identify problems of wider concern in research. Data sources and extraction We tracked key publications that reflected new insights into human methylmercury toxicity. From this evidence, we identified possible caveats of potential significance for environmental health research in general. Synthesis At first, methylmercury research was impaired by inappropriate attention to narrow case definitions and uncertain chemical speciation. It also ignored the link between ecotoxicity and human toxicity. As a result, serious delays affected the recognition of methylmercury as a cause of serious human poisonings in Minamata, Japan. Developmental neurotoxicity was first reported in 1952, but despite accumulating evidence, the vulnerability of the developing nervous system was not taken into account in risk assessment internationally until approximately 50 years later. Imprecision in exposure assessment and other forms of uncertainty tended to cause an underestimation of methylmercury toxicity and repeatedly led to calls for more research rather than prevention. Conclusions Coupled with legal and political rigidity that demanded convincing documentation before considering prevention and compensation, types of uncertainty that are common in environmental research delayed the scientific consensus and were used as an excuse for deferring corrective action. Symptoms of methylmercury toxicity, such as tunnel vision, forgetfulness, and lack of coordination, also seemed to affect environmental health research and its interpretation.

Methylmercury, the causative agent of Minamata disease, can easily penetrate the brain, and adult-type Minamata disease patients showed neurological symptoms according to the brain regions where the neurons, mainly in the cerebrum and cerebellum, were damaged. In addition, fetuses are exposed to methylmercury via the placenta from maternal fish consumption, and high-level exposure to methylmercury causes damage to the brains of infants. Typical patients with fetal-type Minamata disease (i.e., serious poisoning caused by in utero exposure to methylmercury) were born during the period of severe methylmercury pollution in 1955-1959, although they showed no abnormality during gestation nor at delivery. However, they showed difficulties in head control, sitting, and walking, and showed disturbances in mental development, these symptoms that are similar to those of cerebral palsy, during the growth periods after birth. The impaired development of fetal-type Minamata disease patients was one of the most tragic and characteristic feature of Minamata disease. In this review, we first summarize 1) the effects of prenatal methylmercury exposure in Minamata disease. Then, we introduce the studies that were conducted mainly by Sakamoto et al. as follows: 2) a retrospective study on temporal and regional variations of methylmercury pollution in Minamata area using preserved umbilical cord methylmercury, 3) decline in male sex ratio observed in Minamata area, 4) characteristics of hand tremor and postural sway in fetal-type Minamata disease patients, 5) methylmercury transfer from mothers to infants during gestation and lactation (the role of placenta), 6) extrapolation studies using rat models on the effects of prenatal methylmercury exposure on the human brain, and 7) risks and benefits of fish consumption.

Mercury (Hg) and vitamin A (VitA) are two environmental factors with potential health impacts, especially during pregnancy and early childhood. Fish and seafood may present elevated levels of methylmercury (MeHg), the major Hg derivative, and VitA. This study aimed to evaluate the transgenerational effects of exposure to MeHg and/or VitA on epigenetic and toxicological parameters in a Wistar rat model. Our findings revealed persistent toxicological effects in generations F1 and F2 following low/mild doses of MeHg and/or VitA exposure during dams' (F0) gestation and breastfeeding. Toxicological effects observed in F2 included chronic DNA damage, bone marrow toxicity, altered microglial content, reduced neuronal signal, and diminished male longevity. Sex-specific patterns were also observed. Co-exposure to MeHg and VitA showed both synergistic and antagonistic effects. Additionally, the study demonstrated that MeHg and VitA affected histone methylation and caused consistent effects in F2. While MeHg exposure has been associated with transgenerational inheritance effects in other organisms, this study provides the first evidence of transgenerational inheritance of MeHg and VitA-induced toxicological effects in rodents. Although the exact mechanism is not yet fully understood, these findings suggest that MeHg and VitA may perpetuate their impacts across generations. The study highlights the need for remedial policies and interventions to mitigate the potential health problems faced by future generations exposed to MeHg or VitA. Further research is warranted to investigate the transgenerational effects beyond F2 and determine the matrilineal or patrilineal inheritance patterns.

Widespread mercury (Hg) contamination of freshwater systems, due primarily to deposition of atmospheric inorganic Hg (IHg), poses a potential threat to recreational fisheries. In aquatic ecosystems, IHg is converted by bacteria to methylmercury (MeHg), a potent toxin that bioaccumulates in consumers and biomagnifies through the food web, reaching elevated concentrations in fish. Methylmercury has concentration‐dependent sublethal effects on fish, including reductions in reproductive output. In the present study, we conducted the first analysis of the potential health risks of MeHg contamination to largemouth bass (Micropterus salmoides), a popular game fish, in the southeastern United States. To assess the potential health risk posed by MeHg to largemouth bass, we compared MeHg concentrations in three sizes of adult largemouth bass to benchmarks associated with the onset of adverse health effects in fish. We also determined how the risk posed by MeHg to largemouth bass varied spatially throughout the southeastern United States. Our study suggests that in the southeastern United States MeHg poses a potential risk to largemouth bass health and that MeHg contamination may be detrimental to the fisheries of this economically important species of game fish. Environ Toxicol Chem 2023;42:1755–1762. © 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

The Atrato River basin is one of the most biodiverse areas worldwide, and paradoxically, it is one of the sites in Colombia with the highest environmental impact from gold mining. This study assessed the distribution of Hg, As, Pb, and Cd in 47 fish species (n = 1372) and the accumulative human health risk in inhabitants (n = 2325) from 13 municipalities located along the Atrato River basin. The results revealed that Hg and As in fish present a high potential human health risk based on their mean concentrations. Estimated daily intake (EDI) calculations showed that humans could present detrimental health effects, while that target hazard quotient (THQ) above 1 showed that the exposed population might experience noncarcinogenic health risks, mainly from the accumulative effects of Hg (80.4%) and As (18.2%). The species that would most affect the health of the inhabitants are carnivorous H. malabaricus, A. pardalis, P. schultzi, R. quelen, and C. kraussii, which are among the fourteen most consumed in the region. These species had values of estimated weekly intake (EWI) above the provisional tolerable weekly intake thresholds for MeHg (PTWI of 1.6 and 3.2 μg/kg bw/week for adults and children, respectively) in 7 of the 13 localities evaluated. According to the surveys, the calculated weekly allowable fish amount (MFW) showed that carnivorous fish may generate adverse effects on the consumers because the allowed MeHg is about 2 times higher than the upper reference limit. Other results indicate a significant carcinogenic health risk, mainly from As, in 8 of the 13 localities evaluated. Due to the high rates of unsatisfied basic needs and the monetary poverty in the region, the possibility that inhabitants can replace fish as the principal source of protein is low. Therefore, a food guidance is required to avoid risks, obtain nutritional benefits, and sustain fish populations.

In line with the 1000-day initiative and the Sustainable Development Goals (SDG) 2 and 3, we present a cross-sectional analysis of maternal health, infant nutrition, and methylmercury exposure within hard-to-reach indigenous communities in the state of Pará, Brazilian Amazon. We collected data from all women of childbearing age (i.e., 12–49) and their infants under two years old in three Munduruku communities (Sawré Muybu, Sawré Aboy, and Poxo Muybu) along the Tapajos River. We explored health outcomes through interviews, vaccine coverage and clinical assessment, and determined baseline hair methylmercury (H-Hg) levels. Hemoglobin, infant growth (Anthropometric Z scores) and neurodevelopment tests results were collected. We found that 62% of women of childbearing age exceeded the reference limit of 6.0 μg/g H-Hg (median = 7.115, IQR = 4.678), with the worst affected community (Sawré Aboy) registering an average H-Hg concentration of 12.67 μg/g. Half of infants aged under 24 months presented with anemia. Three of 16 (18.8%) infants presented H-Hg levels above 6.0 µg/g (median: 3.88; IQR = 3.05). Four of the 16 infants were found to be stunted and 38% of women overweight, evidencing possible nutritional transition. No infant presented with appropriate vaccination coverage for their age. These communities presented with an estimated Infant Mortality Rate (IMR) of 86.7/1000 live births. The highest H-Hg level (19.6 µg/g) was recorded in an 11-month-old girl who was found to have gross motor delay and anemia. This already vulnerable indigenous Munduruku community presents with undernutrition and a high prevalence of chronic methylmercury exposure in women of childbearing age. This dual public health crisis in the context of wider health inequalities has the potential to compromise the development, health and survival of the developing fetus and infant in the first two critical years of life. We encourage culturally sensitive intervention and further research to focus efforts.

This paper is an exploratory study that examines the illegal goldmining impacts on Munduruku communities’ “Good-Living” (Xipan Jewewekukap) and explores the possible relationship between chronic methylmercury (MeHg) exposure and the worsening mental health conditions in three villages in the Middle-Tapajós River, Brazilian Amazon. The region has been experiencing a long-lasting threat of goldminers’ invasions. A total of 109 people were interviewed and evaluated. Total mercury (THg) exposure levels were evaluated through hair samples analysis, from which MeHg exposure levels were calculated. The Geriatric Depression Scale—Short Form (GDS-SF) was used as a screening tool in order to assess mental health indicators. Brief non-structured interviews were carried out to investigate how goldmining is impacting the communities Good-Living. A Poisson regression model was used to estimate the possible association between mental health indicators (assessed through the GDS-SF) and the following independent variables: (i) mercury exposure level (<10.0 μg/g vs. ≥10.0 μg/g), (ii) self-reported nervousness, (iii) self-reported irritability, (iv) age group, and (v) monthly income. The analysis revealed high levels of mercury in hair samples (median: 7.4 µg/g, range 2.0–22.8; 70% and 28% of the participants had THg levels ≥6.0 and ≥10.0 µg/g, respectively) and pointed to a tendency in which higher levels of methylmercury exposure (Hg ≥ 10.0 µg/g) could be linked to worse mental health indicators. Although the GDS-SF has presented limitations due to the Munduruku sociocultural context, our findings suggest a tendency of worse mental health indicators in participants presenting high levels of MeHg exposure. Despite this limitation, the qualitative approach indicates an evident association between the impacts of goldmining and the Munduruku people’s decreasing autonomy to maintain a Good-Living on their own terms, pointing to the importance of carrying out new investigations, especially considering longitudinal studies with qualitative methodologies and ethnographic approaches.

The environmental contamination by methylmercury (MeHg) is a major concern for public health. The effects of MeHg in the central nervous system (CNS) of adult animals have been extensively investigated; however, little is known about the effects of MeHg exposure during intrauterine and lactation periods on motor and cognitive functions of adolescent rats. Therefore, this study aimed to investigate the effect of MeHg exposure during intrauterine life and lactation on both motor and cognitive functions of offspring rats. Ten female Wistar rats were exposed to 40 μg/kg/day of MeHg through cookie treats from the first day of pregnancy until the last day of breastfeeding. Both motor and cognitive functions of offspring male rats were assessed by open field, rotarod, and step-down inhibitory avoidance tests. Forty-one days after birth, the hippocampus and cerebellum were collected to determine total Hg content, antioxidant capacity against peroxyl radicals (ACAP), reduced glutathione (GSH) levels, lipid peroxidation (LPO), and nitrite levels. MeHg exposure during CNS development increased Hg levels in both hippocampal and cerebellar parenchymas, triggered oxidative stress throughout ACAP and GSH decrease, increased LPO and nitrite levels. These alterations resulted in reduced spontaneous and stimulated locomotion and short- and long-term memory deficits. Therefore, damages triggered by MeHg exposure during intrauterine life and lactation had detrimental effects on oxidative biochemistry and motor and cognitive functions of offspring rats.

Emerging studies have indicated that the consumption of rice could be the major methylmercury (MeHg) contributor to human mercury (Hg) exposure. Nonetheless, few studies are available on Hg in rice around the world, especially in countries with heavy rice diet. In this study, total Hg (THg) and MeHg levels in rice samples (n = 172) across Nepal were first investigated. The geometric mean THg was 7.05 ± 7.71 µg/kg with a range of 0.622 µg/kg to 158 µg/kg, and the maximum THg level was up to 791% of the Chinese National Standard Limit for THg in rice (20 µg/kg). The geometric mean MeHg was 0.820 ± 0.660 µg/kg with a range of 0.189 µg/kg to 8.59 µg/kg. Overall, the mean MeHg exposure (0.00445 ± 0.00477 µg/kg bw/day) and inorganic Hg (IHg) exposure (0.0360 ± 0.0739 µg/kg bw/day) were lower than the reference dose (RfD) of 0.1 µg/kg bw/day for MeHg and the provisional tolerable weekly intake (PTWI) of 0.571 µg/kg bw/day for IHg, respectively. Concerning different groups of vulnerable populations, the highest MeHg exposure (0.126 µg/kg bw/day) and IHg exposure (1.57 µg/kg bw/day) of preschoolers (37-50 months old) were approximately 126% of the RfD for MeHg and 275% of the PTWI for IHg. When the pregnant mothers eat the rice without awareness of the Hg content in rice, the mean and highest intelligence quotients (IQs) losses were 9554 and 118659 points, respectively, and the corresponding economic costs due to IQ loss could be 15.1 million USD and 188 million USD in Nepal. The results of rice THg and MeHg levels and corresponding exposure in populations highlighted the occurrence of rice THg and MeHg pollution issues in Nepal. More efforts should be made to protect younger groups in Nepal from high rice Hg exposure. CAPSULE: Owing to the high rice consumption rates relative to body mass, preschoolers (37-50 months) may meet the 126% reference dose (0.1 µg/kg bw/day) for MeHg and 275% provisional tolerable weekly intake (0.571 µg/kg bw/day) for IHg exposure in Nepal.

Three Gorges Dam (TGD) is the largest hydroelectric construction in the world, and its potential impacts on the ecological environment and human health risks have invoked considerable global concern. However, as a mercury (Hg) sensitive system, limited work was conducted on the Hg exposure level of local residents around the Three Gorges Reservoir (TGR). Thus, 540 human hair samples and 22 species of local food samples were collected to assess the Hg exposure and human health risk to the residents located in the Three Gorges Reservoir Region (TGRR) and to investigate their dietary exposure to Hg. The results showed that the geometric mean concentrations of total mercury (THg) and methylmercury (MeHg) in hair were 0.42 ± 0.43 μg g-1 and 0.23 ± 0.32 μg g-1, respectively, lower than the reference level (1.0 μg g-1) recommended by the United States Environmental Protection Agency (US EPA), indicating a low level Hg exposure for residents around the TGR. No significant difference in the accumulation of Hg in hair between the gender subgroups was observed, whereas age difference, smoking and alcohol drinking behavior, and fish consumption frequency were significant predictors of hair Hg level. Besides, THg and MeHg of all the investigated food samples did not exceed the corresponding Chinese national standard. The average probable daily intakes (PDIs) of THg and MeHg were 0.032 μg kg-1 day-1 and 0.007 μg kg-1 day-1, which were obviously below the recommended values of 0.57 μg kg-1 day-1 and 0.1 μg kg-1 day-1, respectively. The cereal (mainly rice) contribution of THg (76.0%) and MeHg (74.4%) intakes to the local residents around the TGR was much higher than that of fish (10.7% and 22.9%, respectively) due to the considerable rice consumption. Overall, residents around the TGR were at a low Hg exposure and rice consumption was the major pathway for Hg exposure.

Colombia is one of the countries with the highest emissions of mercury (Hg) to the environment, due to its use in gold mining. This study evaluated the human health risk from exposure to Hg through fish consumption in 11 municipalities located in the Mojana region, northern Colombia. The study participants (n = 839) were categorized into three population groups: children (CHD), women of childbearing age (WCHA) and the rest of population (RP). Total Hg (THg) and methylmercury (MeHg) concentrations were evaluated in the top ten most consumed fish species (n = 292). Median concentrations (range: 0.22-0.58 μg/g ww) of the five carnivorous fish species exceeded the reference limit established by FAO/WHO (0.2 μg/g ww) for vulnerable populations. For 6 of the 10 studied fish species, the estimated weekly intake (EWI) in children was above the provisional tolerable weekly intake (PTWI, 1.6 μg/kg bw/week) of MeHg established by JECFA. EWI values for WCHA were above PTWI in 4 fish species, whereas in general, for RP group values were below PTWI (3.2 μg/kg bw/week). Our assessment of potential risks to MeHg exposure indicated that most of the consumed fish could generate negative effects in vulnerable groups, because according to ingestion rate, MeHg permissible is, in some cases, up to 4 times higher than reference limits. Consumption advisories should be a guidance to avoid risk, gain nutritional benefits, and sustain fish populations. Because its high MeHg levels as well as high ingestion, it is recommended that inhabitants of this region should stop eating certain kinds of fish and the whole fish as a single meal. To reduce its harmful intake, we have proposed a didactic strategy based on marbles that control the portion of fish they are eating.

Rice methylmercury (MeHg) contamination has attracted global attention, especially in countries where rice is considered a staple food. The daily rice intake rate in Bangladesh ranks first in the world; however, no attention has been paid to rice MeHg contamination in Bangladesh. Total Hg (THg) and MeHg concentrations of commercial rice (n = 172) from Bangladesh were first analyzed to accurately evaluate both rice MeHg and inorganic Hg (IHg) exposure in different age-gender groups of Bangladeshis. The corresponding adverse health impacts and associated economic loss were also assessed. The results showed that THg concentration in all samples ranged from 0.42 to 14.4 ng/g, with an average of 2.48 ± 1.41 ng/g, while the MeHg concentration ranged from 0.026 to 7.47 ng/g, with an average of 0.83 ± 0.60 ng/g. The highest average MeHg and IHg were both recorded in rice from Chittagong. The highest mean MeHg and IHg exposures were observed in 2-5 years-old group and were 16.2% of the reference dose (RfD) of 0.1 μg/kg/day for MeHg and 7.09% of the provisional tolerable weekly intake (PTWI) of 0.571 μg/kg/day for IHg. Surprisingly, MeHg exposure of the 2-5 year-old children could be up to 93.7% of the RfD at a high percentile (P99.9). The total intelligence quotient reduction caused by rice MeHg exposure could be 54700 points, and the associated economic loss is approximately 42.5 million USD. To avoid high rice MeHg exposure, it was suggested that diet structure be improved. More attention should be paid to residents with long-term rice MeHg exposure, especially children in the 2-5 year-old group.

China is the largest rice producer and consumer in the world, and mercury (Hg) levels, particularly methylmercury (MeHg), in rice and health exposure risks are public concerns. Total Hg (THg) and MeHg levels in 767 (domestic = 709 and abroad = 58) Chinese commercial rice were investigated to evaluate Hg pollution level, dietary exposures and risks of IHg and MeHg. The mean rice THg and MeHg levels were 3.97 ± 2.33 μg/kg and 1.37 ± 1.18 μg/kg, respectively. The highest daily intake of MeHg and IHg were obtained in younger groups, accounted for 6% of the reference dose-0.1 μg/kg bw/day for MeHg, 0.3% of the provisional tolerance week intake-0.571 μg/kg bw/day for IHg. Residents in Central China and Southern China meet the highest rice Hg exposure, which were more than 7 times of those in Northwest China. Lower concentrations than earlier studies were observed along the implementations of strict policies since 2007. This may indicate that a declining temporal trend of Hg in Chinese grown rice and associated exposures could be obtained with the implementations of strict policies. Though there exist Hg pollution in commercial rice, Hg levels in Chinese commercial rice is generally safe compared with Hg polluted sites. Populations dwelling in China have relatively a quite low and safe MeHg and IHg exposure via the intake of commercial rice. Strict policies contributed to the decrease in THg and MeHg levels in Chinese-grown rice. More attention should be paid to younger groups.

Previous research has found that women and children living in rural, interior communities in Suriname have high concentrations of mercury in hair. Freshwater fish from these areas also have high concentrations of mercury. Artisanal and small-scale gold mining operations in parts of the country use elemental mercury to extract gold from soils and sediments. Total mercury and methylmercury concentrations have been determined in hair and blood from pregnant women across the country. Pregnant women from interior communities have significantly higher concentrations of both total and methylmercury in hair (median total mercury in hair 3.64 µg/g) compared with pregnant women from two urban coastal cities, Paramaribo (0.63 µg/g) and Nickerie (0.74 µg/g). Total and methylmercury concentrations in blood and hair are highly correlated ( r  = 0.986, r  = 0.974) with methylmercury making up 86% of the total in blood and 97% of the total in hair. Most women in the interior regions rely heavily on local fish as part of their regular diet, and many live outsides of areas with active ASGM operations. This study demonstrates that diet and fish consumption largely govern mercury exposures in pregnant women in Suriname.

Neurotoxic methylmercury (MeHg) in environments poses substantial risks to human health. Saturated sediments are basic sources of MeHg in food chains; however, distribution patterns and environmental drivers of MeHg at a global scale remain largely unexplored. Here, we characterized global patterns of MeHg distribution and environmental drivers of MeHg production based on 495 sediment samples across five typical ecosystems from the literature (1995-2018) and our own field survey. Our results showed the MeHg concentration ranged from 0.009 to 55.7 μg kg-1 across the different ecosystems, and the highest MeHg concentration and Hg methylation potential were from the sediments of paddy and marine environments, respectively. Further, using combined analysis of random forest and structural equation modeling, we identified temperature and precipitation as important regulators of MeHg production after accounting for the well-known drivers including Hg availability and sediment geochemistry. More importantly, we found increased MeHg production in sediments with elevated mean annual Hg precipitation, and warmer temperature could also accelerate MeHg production by facilitating activities of microbial methylators. Together, this work advances our understanding of global MeHg distribution in sediments and environmental drivers, which are fundamental to the prediction and management of MeHg production and its potential health risk globally.

Worldwide environmental tragedies of anthropogenic origin causing massive release of metals and other pollutants have been increasing considerably. These pollution outbreaks affect the ecosystems and impact human health. Among those tragedies, recent large-scale environmental disasters in Brazil strongly affected riverside populations, leading to high-risk exposure to methylmercury (MeHg). MeHg is highly neurotoxic to the developing brain. This toxicant causes neural stem cell dysfunction and neurodevelopmental abnormalities. However, less is known about the effects of MeHg in the postnatal neurogenic niche, which harbors neural stem cells and their progeny, in the adult brain. Therefore, taking in consideration the impact of MeHg in human health it is urgent to clarify possible associations between exposure to mercury, accelerated cognitive decline, and neurodegenerative diseases. In this perspectives paper, we discuss the neurotoxic mechanisms of MeHg on postnatal neurogenesis and the putative implications associated with accelerated brain aging and early-onset cognitive decline in populations highly exposed to this environmental neurotoxicant.

Background: Methylmercury exposure is a common health risk resulting from daily fish intake. However, studies addressing the link between methylmercury and infertility are limited and also inconsistent. In addition, no previous epidemiological studies have accounted for the interaction between methylmercury and selenium. We aimed to investigate the association between environmental exposures to metals and female fertility. Methods: This case‐control study included 98 infertile women receiving fertility treatment (infertile group) and 43 female workers in their thirties (control group) who provided blood samples and returned a questionnaire on lifestyles and dietary characteristics. Blood levels of mercury, lead, cadmium, arsenic, manganese, zinc, and selenium were compared between the groups. Spearman correlation analyses between anti‐Müllerian hormone and the metals were conducted. Results: The mean selenium level in blood (± SD) and the selenium/mercury molar ratio were significantly lower in the infertile group (189 ± 25 &mgr;g/L and 94.6 ± 44.3, respectively) than in the control group (200 ± 25 &mgr;g/L and 118.4 ± 70.5). By contrast, blood mercury levels after adjusting for blood selenium and age were significantly higher in the infertile group than in the control group. Multiple logistic regression analyses with the adjustment for the other metals and potential confounders confirmed significant associations of infertility with elevated mercury and reduced selenium levels. No significant correlations were observed between anti‐Müllerian hormone and metals. Conclusions: Methylmercury and selenium exposures appear to have adverse and protective effects on female fertility, respectively. This is the first report to suggest the antagonistic interaction between methylmercury and selenium in relation to human female fertility.

Abstract The decline in marine and freshwaters catches in recent years in Colombia has led to a change in dietary habits, with an increase in the purchase and consumption of imported fish. This is of particular concern as fish are sometimes caught in mercury‐contaminated waters, and are subsequently sold canned or uncanned. In addition, canned tuna has received little attention as it is widely assumed that concentrations are low. In this study, total mercury (THg) and methylmercury (MeHg) concentrations were evaluated in three imported fish species marketed in Colombia, Prochilodus lineatus, Prochilodus reticulatus, and Pangasianodon hypophthalmus, plus four brands of canned tuna and one of sardines. One brand of tuna showed the highest mean concentrations of THg (0.543 ± 0.237 &mgr;g/g, wet weight, ww) and MeHg (0.518 ± 0.337 &mgr;g/g ww), while concentrations in P. hypophthalmus were approximately 30 times lower (≈0.02 &mgr;g/g ww). The estimated weekly intake (EWI) in children was above the provisional tolerable weekly intake (PTWI) of MeHg established by the Joint FAO/World Health Organization (WHO) Expert Committee on Food Additives (JECFA) in 2007, 1.6 &mgr;g/kg body weight (bw) per week, for all the canned tuna brands. Values for adults were below PTWI, whereas for women of childbearing age, values were above PTWI only for brand D of canned tuna. The estimate of the potential risk indicated that MeHg levels in canned tuna can generate negative effects in vulnerable groups, while the EWI of fresh fish did not pose a threat to the general population. Therefore, establishing strategies to address the high consumption of canned tuna, and continuous monitoring to control commercial food, are recommended to decrease Hg exposure. HighlightsLevels of Hg species in the most popular imported fish were studied in Colombia.Mean concentrations do not exceeded the maximum levels of Hg permitted in fish.The estimated weekly intakes suggest that children should not eat any can of tuna.Pregnant woman should eat no more than 2 cans of tuna per week (one can from brand D).

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Methylmercury (MeHg) is a globally ubiquitous and persistent environmental toxicant that negatively affects animal behavior, health, and reproduction. In birds, MeHg is transferred from female to egg, contaminating embryos during sensitive stages of early embryonic development and growth. This toxic exposure in the prenatal environment not only induces mortality but also possible lasting impacts on physiology, health, and survival, even once hatched. The purpose of our study was to further elucidate the negative effects of MeHg exposure during avian embryonic development and explore how such exposure can impact offspring development, growth, and survival, both in ovo and posthatch. To assess this, we experimentally dosed fertile mallard and wood duck eggs with MeHg II chloride and reared developing embryos and ducklings to various endpoints. We found that embryos not only readily accumulated MeHg throughout incubation, but they also displayed varying dose-dependent disparities in body mass and morphometrics, with control individuals being larger during early and late embryonic stages of development (p < 0.05). Furthermore, hatched offspring exposed to MeHg exhibited increasingly slower growth rates between 7 to 10 and 10 to 15 days posthatch (p < 0.05), and were found to have lower survival probabilities both under controlled laboratory conditions (p < 0.005), and in the natural environment (p < 0.05). Our findings on the detrimental effects of MeHg on avian embryos and hatchlings emphasize the need for more proactive means of environmental protection and remediation to protect vulnerable avian populations and the ecosystems they inhabit.

No abstract available

From a public health perspective, there is growing concern about dietary mercury intake as the most important source of mercury exposure. This study was performed to estimate dietary mercury exposure and to analyze the association between mercury intake and blood mercury levels in Koreans. The study subjects were 553 adults, comprising a 10% representative subsample of the Korean National Environmental Health Survey (KoNEHS) 2012–2014, who completed a health examination, a face-to-face interview, and a three-day food record. Dietary mercury and methylmercury intakes were assessed from the three-day food record, and blood mercury concentration was measured using a mercury analyzer. The association between dietary mercury intake and blood mercury levels was analyzed by comparing the odds ratios for the blood mercury levels above the Human BioMonitoring (HBM) I value (5 μg/L) among the three groups with different mercury intakes. The average total mercury intake was 4.74 and 3.07 μg/day in males and females, respectively. The food group that contributed most to mercury intake was fish and shellfish, accounting for 77.8% of total intake. The geometric mean of the blood mercury concentration significantly and linearly increased with the mercury and methylmercury intakes (p < 0.001). The odds ratios for blood mercury levels above the HBM I value in the highest mercury and methyl mercury intake group were 3.27 (95% Confidence Interval (CI) 1.79–5.95) and 3.20 (95% CI 1.77–5.79) times higher than that of the lowest intake group, respectively. Our results provide compelling evidence that blood mercury level has a strong positive association with dietary intake, and that fish and shellfish contribute most to the dietary mercury exposure.

ABSTRACT Microbial production of methylmercury from inorganic mercury in rice paddies poses health risks to consumers of this essential dietary staple. Although mercury-methylating communities are well characterized, the microbial guilds contributing to methylmercury accumulation in rice paddies remain unclear. Here, we collected paddy soils across a mercury concentration gradient throughout the rice-growing season to identify microbial and environmental factors influencing methylmercury dynamics. We show that hgcA gene abundance, the key gene required for methylation, was not a significant predictor of methylmercury concentration in paddy soils. We also show that the merB gene abundance correlated with methylmercury in mercury-polluted rhizosphere samples. Methane cycling genes were actively expressed, and their beta-diversity was significantly associated with methylmercury levels. Methanogen abundance correlated with higher methylmercury under elevated total mercury concentrations. Analysis of the methanotroph-associated mbnT gene, implicated in demethylation, revealed an unexpected positive correlation with methylmercury. Multiple regression and machine learning models converged on mercury bioavailability and methanogen/methanotroph abundances as key predictors of methylmercury, with methanogen-associated hgcA gene abundance and methanogen-methanotroph interactions highlighted under flooded, low-redox conditions. These findings suggest that methane-cycling microbes play key roles in methylmercury cycling dynamics and point to management strategies that could simultaneously mitigate mercury pollution and greenhouse gas emissions. IMPORTANCE Methylmercury is a microbially derived neurotoxin that accumulates in the food staple rice (Oryza sativa). Mitigating the health effects of methylmercury exposure requires predicting mercury cycling dynamics in rice paddies. This task is challenging because of the complex interplay of microbial and environmental factors. Our study coupled genomic and geochemical measurements with machine learning models to identify the key biological indicators of methylmercury accumulation. We demonstrated that the abundance of methanogens and methanotrophs is a major microbial predictor of methylmercury variability. This predictive framework, which considers the interactions between these coupled microbial guilds, offers greater power than methods relying only on mercury methylation genes. These findings inform better management and remediation strategies for rice paddies, offering a path to reduce methylmercury exposure and mitigate greenhouse gas emissions. Methylmercury is a microbially derived neurotoxin that accumulates in the food staple rice (Oryza sativa). Mitigating the health effects of methylmercury exposure requires predicting mercury cycling dynamics in rice paddies. This task is challenging because of the complex interplay of microbial and environmental factors. Our study coupled genomic and geochemical measurements with machine learning models to identify the key biological indicators of methylmercury accumulation. We demonstrated that the abundance of methanogens and methanotrophs is a major microbial predictor of methylmercury variability. This predictive framework, which considers the interactions between these coupled microbial guilds, offers greater power than methods relying only on mercury methylation genes. These findings inform better management and remediation strategies for rice paddies, offering a path to reduce methylmercury exposure and mitigate greenhouse gas emissions.

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Despite legal safeguards, the Yanomami community faces challenges such as unauthorized incursions by gold miners, resulting in environmental degradation, particularly from mercury. This jeopardizes the health and food security of indigenous individuals, especially due to the consumption of contaminated fish. Ethnic and racial disparities persist in indigenous healthcare, marked by troubling health indicators such as malnutrition, anemia, and infectious diseases. This cross-sectional study, conducted in October 2022 in the Yanomami Indigenous Territory in the Amazon Forest, Brazil, presented clinical, laboratory, and neurodevelopmental findings in Yanomami children chronically exposed to methylmercury. The results revealed that Yanomami children exhibited weights and heights below expectations (median Z-scores of −1.855 for weight for age and −2.7 for height for age), a high prevalence of anemia (25%), low vaccination coverage (15%), and low IQ (average 68.6). The Total Hair Mercury (Total Hg) levels ranged from 0.16 µg/g to 10.20 µg/g (mean: 3.30 µg/g; median: 3.70 µg/g). Of 117 children tested, 93 children (79.4%) had levels ≥ 2.0 µg/g (had no significant difference between sex). Among the 58 children for whom it was possible to estimate the Total Intelligence Quotient (TIQ), the average value was 68.6, ranging from 42 to 92 points (median: 69.5; standard deviation: 10.5). Additionally, the lowest score on the IQ test was associated with 5 times the risk of having high levels of mercury in their hair, 2,5 fold the risk of having an older age, and almost 8 times the risk of consuming fish, adjusting for nut consumption. Notwithstanding the study’s limitations, results suggest that mercury contamination from illegal mining activities on indigenous lands may negatively impact neurodevelopment in older indigenous children, particularly those fish consumers, despite the inherent benefits of fish consumption. Addressing other socio-environmental concerns is crucial for enhancing the overall health of the population.

Mitigating mercury (Hg) risk in the rice-paddy system is crucial for safeguarding food safety and human health, as rice is a main source of human exposure to neurotoxic methylmercury (MeHg). Current mitigation strategies predominantly focus on reducing the availability of inorganic Hg (IHg) for Hg methylation, achieved primarily through Hg emission control and in situ Hg immobilization. While these IHg-targeted approaches have effectively reduced MeHg bioaccumulation and subsequent human exposure, their efficacy is largely undermined by Hg transformations and fluctuating environmental conditions due to the complex and protracted pathway linking IHg from environmental sources to MeHg at the point of human exposure. In light of recent advancements in MeHg-related transformations, we emphasize the development of MeHg-targeted strategies to improve the overall efficiency of Hg risk management in rice-paddy systems. MeHg-targeted strategies include microbial regulation to diminish net MeHg production, facilitating MeHg demethylation in soils, and promoting the in vivo MeHg degradation within rice plants. Although these approaches are still in their nascent stages, they hold significant promise due to their potential high mitigation efficacy and reduced uncertainties, owing to the shorter pathway between MeHg production and human exposure. Integrating IHg- and MeHg-targeted strategies offers a comprehensive and synergistic approach, paving the way for more effective mitigation of human exposure to MeHg in rice-paddy systems.

The presence of lake ice cover alters the subglacial water environment, thereby influencing the migration and transformation of mercury (Hg) and methylmercury (MeHg) within the ice-water-sediment media of lakes. This study investigated the occurrence characteristics of mercury and methylmercury in various environmental compartments within lakes located at high latitudes in cold regions during the freezing period. To this end, Wuliangsuhai Lake, the largest freshwater lake situated at 40°N in China, was selected as the study site. The contents of mercury and methylmercury in lake ice were determined for the first time. The percentage of methylmercury (MeHg%) and ice-water partition coefficient were analyzed. The pollution situation and health risk were evaluated by single factor pollution index. The results show that the ice body and water body of Wuliangsuhai are not polluted by mercury and methylmercury, but some sampling points in the sediment are slightly polluted. The mercury content in sediment is negatively correlated with the ice thickness, and the methylmercury content in water is positively correlated with the methylmercury content in sediment, but negatively correlated with the ice thickness. The migration ability of methylmercury in ice-water system is stronger than that of mercury. The MeHg% of water in ice period is higher than that in non-freezing period, which is different from other lakes without ice sheet. The results show that in the dynamic equilibrium of methylation and demethylation in the high-latitude lake water, the methylation is higher in the ice period than in the non-freezing period due to the influence of light intensity, while the mercury in the non-freezing period is more susceptible to the demethylation.

Mercury (Hg) is a conspicuous and persistent global pollutant. Ionic Hg can be methylated into noxious methylmercury (CH3Hg), which biomagnifies in marine tropic webs and poses a health risk to humans and organisms. Sediment Hg methylation rates are variable, and the output flux of created CH3Hg are dependent on sediment characteristics and environmental factors. Thus, uncertainties remain about the formation and flux of CH3Hg from sediment, and how this could contribute to the bioaccumulative burden for coastal organisms in shallow ecosystems. Cores were collected from 3 estuarine locations along the Eastern USA to examine how sediments characteristics influence the introduction of Hg and CH3Hg into the base of the food chain. Stable isotopes of inorganic 200Hg and CH3199Hg were injected into sediments of individual cores, with cultured diatoms constrained to overlying waters. Five different treatments were done on duplicate cores, spiked with: (1) no Hg isotopes (control); (2) inorganic 200Hg; (3) CH3199Hg; (4) both 200Hg and CH3199Hg isotopes, (5) both 200Hg and CH3199Hg into overlying waters (not sediment). Experimental cores were incubated for 3 days under temperature and light controlled conditions. These results demonstrate that upper sediments characteristics lead to high variability in Hg cycling. Notably, sediments which contained abundant and peaty organic material (∼28 %LOI), had the highest pore water DOC (3206 μM) and displayed bands of sulfur reducing bacteria yielded the greatest methylation rate (1.97 % day-1) and subsequent diatom uptake of CH3200Hg (cell quota 0.18 amol/cell) in the overlying water.

Elevated CO2 levels and methylmercury (MeHg) pollution are important environmental issues faced across the globe. However, the impact of elevated CO2 on MeHg production and its biological utilization remains to be fully understood, particularly in realistic complex systems with biotic interactions. Here, a complete paddy wetland microcosm, namely, the rice-fish-snail co-culture system, was constructed to investigate the impacts of elevated CO2 (600 ppm) on MeHg formation, bioaccumulation, and possible health risks, in multiple environmental and biological media. The results revealed that elevated CO2 significantly increased MeHg concentrations in the overlying water, periphyton, snails and fish, by 135.5%, 66.9%, 45.5%, and 52.1%, respectively. A high MeHg concentration in periphyton, the main diet of snails and fish, was the key factor influencing the enhanced MeHg in aquatic products. Furthermore, elevated CO2 alleviated the carbon limitation in the overlying water and proliferated green algae, with subsequent changes in physico-chemical properties and nutrient concentrations in the overlying water. More algal-derived organic matter promoted an enriched abundance of Archaea-hgcA and Deltaproteobacteria-hgcA genes. This consequently increased the MeHg in the overlying water and food chain. However, MeHg concentrations in rice and soil did not increase under elevated CO2, nor did hgcA gene abundance in soil. The results reveal that elevated CO2 exacerbated the risk of MeHg intake from aquatic products in paddy wetland, indicating an intensified MeHg threat under future elevated CO2 levels.

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As an extremely dangerous environmental contaminant, methylmercury (MeHg) results in detrimental health effects in human brain nervous system, one of its main targets. However, as a developmental toxicant, the brain of offspring is vulnerable to MeHg during pregnancy and lactation exposure. Unfortunately, mechanisms of neurodevelopmental injuries induced by MeHg have not been fully elucidated. N-acetylcysteine (NAC) has been used for several decades as an antioxidant to antagonize oxidative stress. However, the molecular mechanisms of NAC alleviating MeHg-induced neurodevelopmental toxicity are not clear. Here, for evaluation of the dose-dependent effects of MeHg exposure on neurodevelopmental injuries of offspring, and the possible protective effects of NAC, the pregnant female mice were exposed to MeHg (4, 8, 12 mg/L, respectively) and NAC (50, 100, 150 mg/kg, respectively) from gestational day 1 (GD1) to postnatal day 21 (PND21). Our results indicated that administering MeHg caused behavioral impairment and neuronal injuries in the cerebral cortex of newborn mice. MeHg dose-dependently caused reactive oxygen species (ROS) overproduction and oxidative stress aggravation, together with expression of Nrf2, HO-1, Notch1, and p21 up-regulation, and CDK2 inhibition. NAC treatment dose-dependently antagonized MeHg-induced oxidative stress that may contribute to alleviating neurobehavioral and neurodevelopmental impairments. These results give insight into that NAC can protect against MeHg-induced neurodevelopmental toxicity by its antioxidation capacity.

Methylmercury (MeHg) contamination in rice via paddy soils is an emerging global environmental issue. An understanding of mercury (Hg) transformation processes in paddy soils is urgently needed in order to control Hg contamination of human food and related health impacts. Sulfur (S)-regulated Hg transformation is one important process that controls Hg cycling in agricultural fields. In this study, Hg transformation processes, such as methylation, demethylation, oxidation, and reduction, and their responses to S input (sulfate and thiosulfate) in paddy soils with a Hg contamination gradient were elucidated simultaneously using a multi-compound-specific isotope labeling technique (200HgII, Me198Hg, and 202Hg0). In addition to HgII methylation and MeHg demethylation, this study revealed that microbially mediated reduction of HgII, methylation of Hg0, and oxidative demethylation–reduction of MeHg occurred under dark conditions; these processes served to transform Hg between different species (Hg0, HgII, and MeHg) in flooded paddy soils. Rapid redox recycling of Hg species contributed to Hg speciation resetting, which promoted the transformation between Hg0 and MeHg by generating bioavailable HgII for fuel methylation. Sulfur input also likely affected the microbial community structure and functional profile of HgII methylators and, therefore, influenced HgII methylation. The findings of this study contribute to our understanding of Hg transformation processes in paddy soils and provide much-needed knowledge for assessing Hg risks in hydrological fluctuation-regulated ecosystems.

Methylmercury (MeHg) is a potent neurotoxin and has great adverse health impacts on humans. Organisms and sunlight-mediated demethylation are well-known detoxification pathways of MeHg, yet whether abiotic environmental components contribute to MeHg degradation remains poorly known. Here, we report that MeHg can be degraded by trivalent manganese (Mn(III)), a naturally occurring and widespread oxidant. We found that 28 ± 4% MeHg could be degraded by Mn(III) located on synthesized Mn dioxide (MnO2-x) surfaces during the reaction of 0.91 μg·L-1 MeHg and 5 g·L-1 mineral at an initial pH of 6.0 for 12 h in 10 mM NaNO3 at 25 °C. The presence of low-molecular-weight organic acids (e.g., oxalate and citrate) substantially enhances MeHg degradation by MnO2-x via the formation of soluble Mn(III)-ligand complexes, leading to the cleavage of the carbon-Hg bond. MeHg can also be degraded by reactions with Mn(III)-pyrophosphate complexes, with apparent degradation rate constants comparable to those by biotic and photolytic degradation. Thiol ligands (cysteine and glutathione) show negligible effects on MeHg demethylation by Mn(III). This research demonstrates potential roles of Mn(III) in degrading MeHg in natural environments, which may be further explored for remediating heavily polluted soils and engineered systems containing MeHg.

The past decade witnessed the initiation and boom of the Artisanal and Small-scale Gold Mining (ASGM) activities in the hyper-arid southern Egypt. The ores are mined in the Eastern Desert and then transported to the densely populated farming communities in the Nile Valley, where the river provides the water resources needed for ore processing. In search for economic benefits, the poorly educated farmers with limited technical resources transformed their cultivated lands into ASGM operations, exposing themselves, their families, the residents, and the Nile ecosystems to several environmental and occupational health problems. Using integrated remote sensing, field, geochemical, and isotopic analyses, we report the first inventory of ASGM-related total mercury (THg) and methylmercury (MeHg) levels in tailings, amalgamation-tailing ponds, and surface and groundwater with emphasis on the Edfu city and its surroundings. The field and remote sensing-based mapping of ASGM activities reveals clustering around the Nile waterways and suggests interaction of Hg contamination sources with their surrounding receptors. Common ASGM practices include release of contaminated water from unlined amalgamation-tailing ponds into irrigation and drainage canals, and spreading of tailings over cultivated soils. In a short period (10 years), the released Hg contaminated multiple media, including the surface water, the shallow and deep aquifers, and possibly the soil, crops, and livestock. THg levels in amalgamation-tailing ponds (1200–8470 ng/L) are fourfold higher than US EPA and eightfold the WHO thresholds. The contaminated waters released from amalgamation-tailing ponds raised THg levels in surface water (irrigation canals: 50–100 ng/L; drainage canals: THg: > 200 ng/L) and groundwater (shallow and deep aquifers: 80–500 ng/L). Our findings highlight the need to extend the adopted approach to cover the entire length of the Nile River and its valley and the importance of conducting awareness campaigns to educate residents and health care providers about potential ASGM-related environmental and health hazards. Graphical Abstract

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The outputs of Hg0 and HgII gas generators were validated by isotope dilution with a dynamically generated 199Hg enriched gas standard produced by continuous cold vapour and ICP-MS detection, thereby providing SI-traceability with primary standards.

Throughout the past four decades, most projects related to mercury in Artisanal Gold Mining (AGM) have been dedicated to monitoring the environmental and health impacts of the activity without actually proposing effective solutions to tackle the issue. Recently, the UN and a few NGOs have been dedicated to bringing solutions to artisanal gold miners, but the outcomes remain modest, given the funds expended and the considerable effort invested by interventionists. This commentary paper critiques some of the interventions observed in the last four decades and suggests some technical strategies to approach artisanal miners to reduce mercury losses. It is stressed that mercury elimination is a consequence of good engagement with miners that creates opportunities to show them how to produce more gold with cleaner methods. We recommend that academics educate a new generation of engineers working with AGM to adopt a more practical approach, ensuring they understand the needs, motivations, and skills of artisanal miners before proposing solutions.

Mercury ion (Hg2+), a highly toxic metal pollutant, is widely found in the environment and can enter the human body through the food chain, causing various health issues. Sensitive and accurate methods for monitoring Hg2+ are highly desirable for ensuring food safety. Herein, we propose a self-sustainable multiple amplification system (MAS) for Hg2+ determination through the reciprocal activation between catalytic hairpin assembly (CHA) and rolling circle amplification (RCA). The thymine-encoded recognition element specifically recognizes Hg2+, triggering the exposure of the initiator. The initiator then motivates the mutual activation of CHA and RCA to accelerate the production of an exponentially amplified signal. The MAS method achieved a low detection limit of 11 pM. Due to its reliable target recognition and robust amplification efficiency, the MAS circuit facilitated the highly efficient and accurate analysis of low-abundance Hg2+ in milk and snakehead samples, thus providing a potentially new tool for food safety control.

Due to rapid industrialization coupled with indiscriminate release of pollutants, the number of polluted rivers in Malaysia has been steadily increasing over the years. Regular monitoring of contaminants, particularly heavy metals, is not feasible due to the steep cost of instrumental monitoring alone. In this study, a rapid inhibitive enzyme assay using the molybdenum-reducing enzyme from the bacterial isolate 34XW was developed for monitoring mercury. The Mo-reducing enzyme from this bacterium was very sensitive to mercury, with an IC₅₀ confidence interval of 0.0025–0.0029. The inhibition model followed a log(inhibitor) vs. response with variable slope, enabling detection of mercury at the Maximum Permissible Limit (MPL) set by the Malaysian Department of Environment. Comparisons with established assays, using IC₅₀ values and confidence intervals, confirmed the superior sensitivity of the developed method. Hierarchical clustering identified patterns of enzyme sensitivity, with assays grouped by IC₅₀ intervals. Isolate 34XW was an outlier with exceptional sensitivity. K-Means clustering grouped assays into sensitivity tiers, with the clustering of the molybdenum-reducing enzyme from the bacterial isolate 34XW into a unique cluster due to the level of its sensitivity. Juru industrial estate water samples tested using the assay revealed its capability in detecting low concentrations of mercury. These findings underscore the assay’s utility in detecting elevated mercury concentrations in environmental samples and its broader implications for environmental monitoring and biochemical applications. As a preliminary screening tool for heavy metal monitoring on a large scale, the assay is quick and easy to use.

Potentially toxic elements (PTEs) have become a significant global concern due to their detrimental effects on both ecological and public health. Monitoring these elements is crucial in areas suspected of having high concentrations. In Camarines Norte, small-scale gold mining (SSGM) activities have been linked to elevated mercury levels in soils and sediments, as it is commonly used in the gold extraction process. In this study, six (6) SSGM wastes from Camarines Norte were collected, analyzed, characterized, and assessed for pollution by eight (8) PTEs: arsenic (As), cadmium (Cd), chromium (Cr), copper (Cu), nickel (Ni), lead (Pb), zinc (Zn), and mercury (Hg). Analytical techniques such as energy dispersive x-ray fluorescence (EDXRF), x-ray diffraction (XRD), inductively coupled plasma – mass spectrometry (ICP-MS), and direct mercury analyzer (DMA) were utilized. Analysis shows quartz (SiO?) as the primary mineral among all samples, with some also containing albite, biotite, kaolinite, microcline, and sphalerite. Pollution was assessed using enrichment factor (EF) and index of geoaccumulation (Igeo), which showed that the SSGM waste samples were extremely enriched and contaminated with As, Cd, Cu, Hg, Pb, and Zn. Gold concentrations were also measured, revealing high levels of enrichment in the samples. Furthermore, one of the SSGM waste samples underwent Hg leaching using environmentally friendly solvents, including deep eutectic solvents (DES). The reduced mercury concentrations after leaching demonstrate the potential application of DES for mercury remediation.

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Summary Pollution, causing millions of deaths annually, disproportionally affects low- and middle-income countries (LMICs). Mercury ranks among the three main chemicals of major public health concern, and even low levels can cause cardiovascular and nervous outcomes, with children and indigenous populations being especially vulnerable. Nearly 80% of all emissions in South America originate from the Amazon. Brazil, the fifth-largest contributor to global mercury emissions, exemplifies the challenges faced by LMICs in effectively monitoring and addressing mercury exposure/intoxication. Despite having powerful tools such as SINAN (a digital platform for compulsory disease reporting), and Community Health Agents, data reveals significant underreporting, especially in the Amazon. Furthermore, SINAN has important delays in its update: for instance, 196 cases of Munduruku Indigenous people in 2019 have only been included in 2023. In this Personal View, we outline insightful recommendations to enhance public health surveillance and implement enduring, effective strategies to monitor, report and address mercury exposure/intoxication, focusing on the Brazilian Amazon. Although these recommendations are tailored to the challenges of this country, they hold potential for adaptation by other Amazonian countries facing similar issues (high mercury emissions and the presence of vulnerable populations, among others).

Heavy metal ion pollution poses a significant threat to environmental and human health. We developed a highly selective and sensitive electrochemical sensor for mercury(II) detection, utilizing a synthesized nickel(II) complex, [(5,10,15,20-tetrakis(p-bromophenyl)porphyrinato] Nickel(II) [Ni(TBrPP)]. The structural integrity, composition, and physicochemical properties of [Ni(TBrPP)] were characterized using a comprehensive set of analytical techniques, including Proton nuclear magnetic resonance, UV-Vis spectroscopy, and infrared spectroscopy, confirming structural integrity and optical properties. Its chemical structure and functional groups were elucidated, and its photophysical properties were investigated to assess optical behavior and electronic transitions. Electrochemical performance of the sensor was evaluated using cyclic voltammetry and differential pulse voltammetry, revealing an optimal response at pH 5. The sensor demonstrated exceptional selectivity for mercury(II), exhibiting minimal interference from competing metal ions such as Cadmium(II), Zinc(II), Copper(II), Manganese(II), and Lead(II) at 10 µM concentrations. With a detection limit of 6 nM, a linear response range of 0.006–10 µM, and a sensitivity of 6.939 µA/µM, the sensor proves highly effective for mercury detection. Excellent stability and reproducibility in real sample analysis yielded recovery rates between 96% and 103%, underscoring its robustness and accuracy for practical applications.

Mercury (Hg) is an environmentally hazardous metal and pollutant in key European legislation pertaining to the marine environment (the Water Framework Directive WFD and the Marine Strategy Framework Directive - MSFD).Despite the environmental importance of Hg there is limited knowledge on levels in Greek waters. This paper presents the first attempt to evaluate THg (total Mercury) levels in the coastal waters of Greece in a decade of monitoring (2012-2022) and identify trends and spatial patterns. These results represent the first seawater Hg data reported by Greece under the WFD, highlighting the importance of this work in understanding Hg pollution in Greek coastal waters. The THg levels measured in all areas were well below the European Legislation threshold of 70 ng/L (EC 2013/39). The overall dataset median was 1.65 ng/L. Increased levels of Hg were found, as expected, near the major cities of Greece (Athens, Thessaloniki) and the major rivers of Northern Greece as well as in some of smaller ports (Piraeus, Rafina, Lavrio etc.). The area that stands out as a distinct 'hot spot' is the Saronikos Gulf, particularly Elefsina Bay, where Hg concentrations are significantly elevated.

South Africa stands out as a prominent global contributor of mercury (Hg) emissions, a matter of great concern due to its toxic nature and potential serious health effects on biota if it enters the environment. Mercury enters freshwater systems through various anthropogenic activities, such as emissions from coal-fired power stations and artisanal gold mining. Studies have indicated that bivalves accumulate metals from their aquatic environment. The freshwater bivalve genus Corbicula is widely distributed across South Africa and is relatively abundant. Given the widespread presence of Corbicula clams in South Africa, they have the potential to serve as bioindicators for Hg pollution in freshwater ecosystems. A total of 34 sites were sampled across the northeastern part of South Africa, with Corbicula clams found at 15 of these sites. At each site, a minimum of five clams were collected, alongside water and sediment samples. Total Hg (THg) concentrations were determined in sediment and clam samples using a flow injection mercury system. Total Hg concentrations in sediment samples correlated with different land-use activities, where sites closer to Hg sources had higher THg concentrations. This study also found higher environmental THg concentrations in the Olifants, and Inkomati Water Management Areas as reported 12 years ago. Clam THg concentrations were found to be higher than in the corresponding sediment samples, specifically in larger clams, suggesting longer Hg exposure at some sites. A weak positive correlation was found between sediment and clam THg concentrations, suggested that bioaccumulation may be influenced more by exposure period, rather than exposure concentrations. This study highlights the potential for these clams to serve as effective bioindicators since the accumulation of THg in their tissue can provide a better overview of the bioavailable THg in the aquatic system, compared to abiotic environmental samples alone.

The aim of the work is to study mercury pollution of components of aquatic ecosystems of the Lower Don, since mercury is a widespread pollutant in water bodies with high toxicity for living organisms and the ability to bioaccumulate. Materials and methods . The results of studies of mercury content in water, bottom sediments and aquatic organisms in the lower reaches of the Don River, collected at 10-25 stations during the period 1995-2024 in the spring, summer and autumn seasons, are presented. Mercury was determined using the cold vapor atomic absorption method. Results : in 1995-2005, the mercury concentration in the water of the Lower Don was high on average, then for 15 years its content was at a low level, and from 2020 to 2024, cases of high mercury concentrations began to be recorded again, with maximums in the area of the Romanovskaya station (up to 62 MPC) and the city of Semikarakorsk (up to 140 MPC). In 2022, in the spring-summer period of the year in the area of st. Romanovskaya, mercury accumulation was detected not only in the water, but also in bottom sediments. In the modern period, a higher mercury content has been noted in the muscles of predatory fish species without exceeding the permissible level. The novelty : for the first time, data on mercury content in water and bottom sediments of the Lower Don over 30 years of observations and aquatic bioresources in the modern period (2020-2024) were summarized and analyzed. Practical significance : the obtained results were used to establish safety criteria for the waters of the Lower Don and commercial fish in accordance with the standard of maximum permissible mercury concentration for fishery waters adopted in Russia and the requirements of the Technical Regulations of the Customs Union.

Since black-tailed gulls derive energy for egg production around their habitat, analyzing concentration of chemicals in the eggs reveals the local environmental pollution. This is, however, complex due to the diversity of seabird diets across multiple ecosystems. This study determined the influence of food source and trophic position (TP) on the mercury concentration ([Hg]) in eggs and subsequently mitigated these influences by adjusting through [Hg]-TP relationship, thereby enabling spatial and temporal comparisons among individuals. Following TP adjustment, the [Hg] that previously exhibited significant regional differences no longer displayed such a variation. Moreover, by normalizing to trophic level 4, as suggested by the European Union (EU), the total [Hg] was standardized from 1001 ± 415 ng g-1 to 1347 ± 516 ng g-1 in all the egg samples, far exceeding the EU criteria. These two approaches provide valuable insights for the effective monitoring of marine pollution and past environmental reconstruction by adjusting/normalizing [Hg] in seabird eggs.

In the southeast and east coasts of the Republic of Korea, it is essential to monitor mercury accumulation in coastal organisms in view of the higher mercury distribution in sediments and human samples. However, mercury pollution monitoring in organisms, especially higher trophic-level organisms that can exhibit high mercury accumulation, is limited. Here, we examined the applicability of the eggs of the black-tailed gull (Larus crassirostris), which belongs to a high trophic level, for mercury monitoring in coastal areas. Breeding sites were selected in West, Southeast, and East Seas with different mercury concentrations in other matrices (sediment and biological samples of residents). The 5-year mean total mercury concentration in eggs collected during the breeding seasons from 2016 to 2020 was lower in Baengnyeongdo (705 ± 81 ng/g dry weight (dry), West Sea) than in Hongdo (1,207 ± 214 ng/g dry, Southeast Sea) and Ulleungdo (1,095 ± 95 ng/g dry, East Sea). The different patterns of mercury concentration in gull eggs among the breeding sites was consistent with those in the other matrices among the coastal areas. These results support the applicability of the black-tailed gull egg as an indicator for establishing a monitoring framework in the coastal areas of the Republic of Korea.

Mercury (Hg) is a global pollutant that is a major public health concern due to its mobility, stability and toxicity behavior in the environment. In this study Hg concentrations were determined in beach sediment samples (n = 43) collected from the South Durban Coast, South Africa. A human health risk assessment was also carried out to comprehend the potential health effects of incidental ingestion/direct contact with contaminated sediments in a recreational setting. Hg concentrations ranged between 0.62 and 4.88 mg kg-1 dw., exceeding all background and regulatory limits. Numerical values of calculated exposure pathways represented dermal contact with the sediments as one of the potential paths in both adults and children. Hazard Index (HI) values were found to be less than unity signifying no adverse health effects. This study validates the critical need for long-term monitoring of Hg in various scenarios in order to incorporate better public health management strategies.

The goal of this paper is to assess the current status and trends of total mercury (THg) contamination of the atmosphere and terrestrial ecosystems in Poland. The study shows that the reduced domestic and worldwide atmospheric emission of Hg resulted in decreased THg level in the terrestrial biotope and biosphere. Considering that Poland is one of the main Hg emitters in Europe, the THg concentrations in its abiotic environment are still elevated. However, the THg level in terrestrial organisms is relatively low, which is because a large proportion of Hg deposited on land is accumulated in organic-rich soils. Regarding the THg concentration, consumption of wildlife and livestock from Poland is safe for humans. Nevertheless, the authors indicate the need for effective environmental monitoring, based on selected bioindicators, which is crucial considering the slowing reduction of Hg emission combined with the consequences of the changing climate.

With increasing industrial activities, mercury has been largely discharged into environment and caused serious environmental problems. The growing level of mercury pollution has become a huge threat to human health due to its significant biotoxicity. Therefore, the simple and fast means for on-site monitoring discharged mercury pollution are highly necessary to protect human beings from its pernicious effects in time. Herein, a "turn off" fluorescent biosensor (mCherry L199C) for sensing Hg2+ was successfully designed based on direct modification of the chromophore environment of fluorescent protein mCherry. For rapid screening and characterization, the designed variant of mCherry (mCherry L199C) was directly expressed on outer-membrane of  Escherichia coli cells by cell surface display technique. The fluorescent biosensor was characterized to have favorable response to Hg2+ at micromole level among other metal ions and over a broad pH range. Further, the cells of the fluorescent biosensor were encapsulated in alginate hydrogel to develop the cells-alginate hydrogel-based paper. The cells-alginate hydrogel-based paper could detect mercury pollution in 5 min with simple operation process and inexpensive equipment, and it could keep fluorescence and activity stable at 4 °C for 24 hr, which would be a high-throughput screening tool in preliminarily reporting the presence of mercury pollution in natural setting.

This article presents the initiation and implementation of a systematic scientific and political cooperation in the Arctic related to environmental pollution and climate change, with a special focus on the role of the Arctic Monitoring and Assessment Programme (AMAP). The AMAP initiative has coordinated monitoring and assessments of environmental pollution across countries and parameters for the entire Arctic region. Starting from a first scientific assessment in 1998, AMAP's work has been fundamental in recognizing, understanding and addressing environmental and human health issues in the Arctic, including those of persistent organic pollutants (POPs), mercury, radioactivity, oil, acidification and climate change. These scientific results have contributed at local and international levels to define and take measures towards reducing the pollution not only in the Arctic, but of the whole globe, especially the contaminant exposure of indigenous and local communities with a traditional lifestyle. The results related to climate change have documented the rapid changes in the Arctic and the strong feedback between the Arctic and the rest of the world. The lessons learned from the work in the Arctic can be beneficial for other regions where contaminants may accumulate and affect local and indigenous peoples living in a traditional way, e.g. in the Himalayas. Global cooperation is indispensable in reducing the long-range transported pollution in the Arctic.

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This paper discusses the results of the monitoring of anthropogenic mercury contamination of the upper part of Bratsk reservoir. The paper shows that in the long-term, (1998-2018) there is an ongoing decrease of Hg concentration in the surface layer of bottom sediments. At the same time the study demonstrates that 20 years after the cessation of mercury electrolysis at the Usoliehimprom chemical plant, Hg concentration in the bottom sediments exceeds background levels by 5 to 54 times. Significant part of the Hg in the bottom sediments is stored in organic form, which is potentially dangerous since it may cause secondary contamination of aquatic environment and hydrobionts. The high amplitude of water-level fluctuations in the reservoir is one of the main factors influencing the distribution of mercury in the surface layer of bottom sediments and preventing the sealing of contaminated bottom sediments by terrigenous material.

This article discusses the results of a pilot research strategy for monitoring environmental hazards derived from the use of mercury in artisanal gold mining in the Alto Cauca region, Colombia. During 2016 and 2017, a transdisciplinary approach was established to inquire on the health, environment, and territorial problems originated from artisanal mining. In this article, we specifically focus on how this particular issue affects women in the area. We establish a closed-loop approach for integrating social action research with analytical sciences/engineering to understand risks associated with Hg2+ levels in artisanal and small-scale gold mining in the Cauca department. We develop a platform known as closed-loop integration of social action and analytical chemistry research.

Global mercury pollution has markedly and consistently grown over the past 70 years (although with regional variations in trends) and is a source of major concern. Mercury contamination is particularly prevalent in biota of the mesopelagic layers of the open ocean, but these realms are little studied, and we lack a large scale picture of contamination in living organisms of this region. The Bulwer's petrel Bulweria bulwerii, a species of migratory seabird, is a highly specialised predator of mesopelagic fish and squid, and therefore can be used as a bioindicator for the mesopelagic domain. Mercury accumulated by the birds through diet is excreted into feathers during the moulting process in adults and feather growth in chicks, reflecting contamination in the non-breeding and breeding periods, respectively, and hence the influence of different, largely non-overlapping breeding and non-breeding ranges. We studied mercury in feathers and the trophic position in two colonies from the Atlantic Ocean (Portugal and Cape Verde) and two colonies from the Pacific Ocean (Japan and Hawaii). We found significantly lower levels of mercury in adult and chick samples from the Pacific Ocean compared with samples from the Atlantic Ocean. However, we did not detect differences in trophic position of chicks among colonies and oceans, suggesting that differences in mercury measured in feathers reflect levels of environmental contamination, rather than differences in the structure of the trophic chain in different oceans. We conclude that despite a reduction in mercury levels in the Atlantic in recent decades, mesopelagic organisms in this ocean remain more heavily contaminated than in the Pacific at tropical and subtropical latitudes. We suggest that Bulwer's petrel is a highly suitable species to monitor the global contamination of mercury in the mesopelagic domain.

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Studies on the monitoring of mercury accumulation using high trophic-level predators of the marine ecosystem have been scarce in South Korea. In this study, we compared the mercury concentrations of the eggs of the black-tailed gulls, a higher-order predator, breeding in two coastal areas. Breeding sites with varying mercury concentrations in land-origin freshwater fish and freshwater and marine sediments were selected in the southeastern (Hongdo Island) and western (Baengnyeongdo Island) seas. The 5-year mean total mercury concentration in eggs collected during the breeding seasons from 2012 to 2016 was higher in those collected from Hongdo than in those collected from Baengnyeongdo. This difference in mercury concentration in eggs was observed for each year. In addition, the total mercury concentration in eggs was consistently higher on Hongdo, which also had higher mercury pollution, than on Baengnyeongdo Island. These results support the suitability of black-tailed gull eggs for monitoring of mercury pollution.

Potentially toxic metals pollution in the Straits of Malacca warrants the development of rapid, simple and sensitive assays. Enzyme-based assays are excellent preliminary screening tools with near real-time potential. The heavy-metal assay based on the protease ficin was optimized for mercury detection using response surface methodology. The inhibitive assay is based on ficin action on the substrate casein and residual casein is determined using the Coomassie dye-binding assay. Toxic metals strongly inhibit this hydrolysis. A central composite design (CCD) was utilized to optimize the detection of toxic metals. The results show a marked improvement for the concentration causing 50% inhibition (IC50) for mercury, silver and copper. Compared to one-factor-at-a-time (OFAT) optimization, RSM gave an improvement of IC50 (mg/L) from 0.060 (95% CI, 0.030–0.080) to 0.017 (95% CI, 0.016–0.019), from 0.098 (95% CI, 0.077–0.127) to 0.028 (95% CI, 0.022–0.037) and from 0.040 (95% CI, 0.035–0.045) to 0.023 (95% CI, 0.020–0.027), for mercury, silver and copper, respectively. A near-real time monitoring of mercury concentration in the Straits of Malacca at one location in Port Klang was carried out over a 4 h interval for a total of 24 h and validated by instrumental analysis, with the result revealing an absence of mercury pollution in the sampling site.

An important provision of the Minamata Convention on Mercury is to monitor and evaluate the effectiveness of the adopted measures and its implementation. Here, we describe for the first time currently available biotic mercury (Hg) data on a global scale to improve the understanding of global efforts to reduce the impact of Hg pollution on people and the environment. Data from the peer-reviewed literature were compiled in the Global Biotic Mercury Synthesis (GBMS) database (>550,000 data points). These data provide a foundation for establishing a biomonitoring framework needed to track Hg concentrations in biota globally. We describe Hg exposure in the taxa identified by the Minamata Convention: fish, sea turtles, birds, and marine mammals. Based on the GBMS database, Hg concentrations are presented at relevant geographic scales for continents and oceanic basins. We identify some effective regional templates for monitoring methylmercury (MeHg) availability in the environment, but overall illustrate that there is a general lack of regional biomonitoring initiatives around the world, especially in Africa, Australia, Indo-Pacific, Middle East, and South Atlantic and Pacific Oceans. Temporal trend data for Hg in biota are generally limited. Ecologically sensitive sites (where biota have above average MeHg tissue concentrations) have been identified throughout the world. Efforts to model and quantify ecosystem sensitivity locally, regionally, and globally could help establish effective and efficient biomonitoring programs. We present a framework for a global Hg biomonitoring network that includes a three-step continental and oceanic approach to integrate existing biomonitoring efforts and prioritize filling regional data gaps linked with key Hg sources. We describe a standardized approach that builds on an evidence-based evaluation to assess the Minamata Convention’s progress to reduce the impact of global Hg pollution on people and the environment.

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Long-term monitoring of data of ambient mercury (Hg) on a global scale to assess its emission, transport, atmospheric chemistry, and deposition processes is vital to understanding the impact of Hg pollution on the environment. The Global Mercury Observation System (GMOS) project was funded by the European Commission (http://www.gmos.eu) and started in November 2010 with the overall goal to develop a coordinated global observing system to monitor Hg on a global scale, including a large network of ground-based monitoring stations, ad hoc periodic oceanographic cruises and measurement flights in the lower and upper troposphere as well as in the lower stratosphere. To date, more than 40 ground-based monitoring sites constitute the global network covering many regions where little to no observational data were available before GMOS. This work presents atmospheric Hg concentrations recorded worldwide in the framework of the GMOS project (2010-2015), analyzing Hg measurement results in terms of temporal trends, seasonality and comparability within the network. Major findings highlighted in this paper include a clear gradient of Hg concentrations between the Northern and Southern hemispheres, confirming that the gradient observed is mostly driven by local and regional sources, which can be anthropogenic, natural or a combination of both.

Low-level pollution accidents are keeping increasing and difficult to monitor in real time. In our current study, zebrafish are used as a common freshwater model to monitor low-level concentrations of 0.05 mg·L−1 mercuric chloride (HgCl2). Avoidance (swimming increased and closely gathered) was the first response, but those abnormal behaviour just lasted 15~20 min and then recovered to the original level with much more fluctuation. In order to quantitative evaluate the first stress responses of fish exposed to lower concentration of toxicant, entropy is proposed for detecting the first responses. The use of entropy contributed to the reliability and precision for detecting toxicant at lower concentration pollution.

Many researchers have developed selective catalytic reduction (SCR) and activated carbon injection (ACI) technologies to control gaseous mercury emissions from coal‐fired power plants, which pose serious risks to human health and ecosystems. This study employs life cycle assessment (LCA) to compare the environmental impacts of SCR and ACI for gaseous elemental mercury (Hg 0 ) removal. To eliminate annual mercury emissions equivalent to 78 kg‐Hg 0 , SCR (0.027 kPt) exhibits a substantially lower environmental burden than ACI (0.483 kPt), which requires greater material and energy inputs. Sensitivity analysis identifies key parameters—catalyst replacement cycle (2–4 years), vanadium content (1%–2.5%), adsorbent efficiency (50%–100%), adsorbent performance (2.36–44.84 μg‐Hg 0 /g‐Biochar), and biomass sourcing (free supply, rice husk, and wheat straw)—all of which, except biomass sourcing, show an inverse correlation with total environmental impact. Notably, the long‐term environmental burden of ACI exceeds that of untreated mercury emissions, primarily due to high diesel consumption for landfill maintenance. Overall, the results suggest that SCR represents a more sustainable option for mercury emission control in coal‐fired power plants.

In order to comprehensively evaluate the environmental impact of multi-media mercury pollution under differentiated emission control strategies in China, a literature review and case studies were carried out. Increased human exposure to methylmercury was assessed through the dietary intake of residents in areas surrounding a typical coal-fired power plant and a zinc (Zn) smelter, located either on acid soil with paddy growth in southern China, or on alkaline soil with wheat growth in northern China. Combined with knowledge on speciated mercury in flue gas and the fate of mercury in the wastewater or solid waste of the typical emitters applying different air pollution control devices, a simplified model was developed by estimating the incremental daily intake of methylmercury from both local and global pollution. Results indicated that air pollution control for coal-fired power plants and Zn smelters can greatly reduce health risks from mercury pollution, mainly through a reduction in global methylmercury exposure, but could unfortunately induce local methylmercury exposure by transferring more mercury from flue gas to wastewater or solid waste, then contaminating surrounding soil, and thus increasing dietary intake via crops. Therefore, tightening air emission control is conducive to reducing the comprehensive health risk, while the environmental equity between local and global pollution control should be fully considered. Rice in the south tends to have higher bioconcentration factors than wheat in the north, implying the great importance of strengthening local pollution control in the south, especially for Zn smelters with higher contribution to local pollution.

Optimum control of mercury released from the coal-fired power plant is evaluated by determining its efficiency and appropriateness in reducing emissions and ambient air concentrations. The 2400 MW power plant fueled by lignite located in Thailand is demonstrated in this study. Emissions of mercury from the coal-fired power plant are calculated under 3 major scenarios. The first scenario is the amount of mercury released under the existing operation of the power plant. Emission rate of mercury is calculated as 41 g/h which indicates a co-benefit of mercury removal from the installation of existing conventional air pollution treatment systems (electrostatic precipitator and wet flue gas desulfurization) as compare with the 2nd scenario of without equipping of air pollution control devices at the power plant (374 g/h of mercury emission). Adding controlling measures to existing operation of the power plant can lead to decreasing of mercury emissions at different levels. The relationship between changing of emissions affected to ambient air concentrations of mercury is evaluated using the CALPUFF air dispersion model. Results indicate small decreasing of predicted ambient concentrations after applying additional mercury control measures to the BAU of the power plant. This study reveals the co-benefit of existing air pollution treatment devices in controlling mercury emission. It also illustrates that the efficiency and appropriateness of current air pollution control system is in an optimal and acceptable levels in mercury control. Finding and methodology in this study can be used as a case study in quantitative evaluation of the effectiveness and appropriateness of environmental control mitigation measures added to the existing operations. It clearly illustrates the need to analyze the co-benefit of current air pollution control system towards the accomplishment on controlling emissions of other emerging air pollutants which will provide the best optimum air pollution control to the emission source.

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Anthropogenic mercury (Hg) emission inventories are crucial for the effectiveness evaluation of the Minamata Convention on Mercury. In this study, we developed an integrated Dynamic Inventory for Mercury Emission (DIME) model and improved the accuracy of emission estimates for primary sources in China. Long-term historical speciated Hg emission inventories for China were established. The total Hg emissions increased from 217.0 t in 1980 to 357.8 t in 2020 with a peak value of 506.6 t in 2010. Three stages with distinct leading drivers were identified. At Stage 1 (1980-1997), Hg emissions doubled with the rapid growth of economy; the driver was offset by the increase of dust and SO2 control measures at Stage 2 (1997-2010) except for cement production; and co-benefits from strict control measures induced the decoupling of Hg emissions from the economy at Stage 3 (2010-2020). The ultralow emission (ULE) retrofits in key industries had pronounced Hg removal efficiencies. Large emission reduction potential still exists in the cement industry. The improved emission estimation methods for key sectors, the consistency in methodology for historical Hg emission inventories, and the more accurate spatial distribution of speciated Hg emissions in this study provide a practical toolkit for the effectiveness evaluation of the Minamata Convention.

Coal-fired industrial boilers (CFIBs) are a priority for air pollution control and the leading sources of mercury (Hg) emissions. However, specific quantitative research on its impact on emission reduction remains limited. The spatial and temporal evolution of atmospheric Hg emissions from CFIBs in China was investigated in detail by establishing atmospheric Hg emission inventories at the technology level and facility level for the years 2000-2019 and 2020-2060. In addition, the impacts of various measures on atmospheric Hg emissions were quantitatively assessed. Results indicated that there was a 54 % rise in atmospheric Hg emissions between 2000 and 2012, followed by an 87 % decline between 2012 and 2020. During this period, the proportion of atmospheric Hg emissions increased by 10.3 % during the winter months. From 2020-2060, atmospheric Hg emissions were projected to decline annually, resulting in a total reduction ranging from 37.2 % to 58.8 %. The rate of decline was higher in general areas than in focus areas during this period. Our findings offer a more precise and detailed atmospheric Hg emission inventory from Chinese CFIBs, enabling the development of targeted control strategies and the management of atmospheric Hg emissions with regional differentiation.

Mercury pollution has attracted worldwide attention due to its toxicity, bioaccumulation and persistence. Cement clinker production is the top emitter of atmospheric mercury in China and the emissions from raw mill systems account for about 85% of all emissions. However, the mercury emission characteristics and mechanisms as a function of time during an operation cycle are still unclear. This study aims to reveal the mercury emission characteristics and mechanisms in cement plants by comprehensively using offline and online field measurements, control experiments and heat transfer analysis. Research results indicated that an intermediate temperature (300-500 °C) desorption and the heterogeneous oxidation of mercury in the precalciner, the selective adsorption of oxidized gaseous mercury (Hg2+) to raw meal, and Hg2+ re-vaporization in the conditioning tower jointly caused an increase in the Hg2+ ratio (15.3%-83.6%) during the mill-off mode. In addition, mercury concentrations remained at approximately 6.5 μg/Nm3 during the mill-on mode while the values reached a peak of 1835.4 μg/Nm3 during the mill-off mode. Thus, atmospheric mercury emissions during the mill-off mode accounted for 35.0%- 71.7% of the emissions during the entire cycle, although the mill-off period only lasted for 5%- 17% of the whole cycle. Our results therefore suggest that supervisory monitoring of mercury in cement clinker production should specify the operating status of raw mills. Mercury control technologies targeting a relatively short period for the mill-off mode can substantially reduce mercury emissions from cement clinker production, and thus, the related impacts on ecosystems and human health.

Nonferrous metal smelting (NFMS) is one of the key sources of mercury (Hg) emissions to the air and cross-media Hg transfer in China. In this study, a "Hg removal compensation effect" between upstream and downstream air pollution control devices (APCDs) in NFMS was uncovered based on the investigation of field test data. The relationships between the Hg concentration in flue gas and the Hg removal efficiencies of typical APCDs were established, and an advanced probabilistic mass flow model regarding this effect was developed. Model comparison shows that the probabilistic essence of the advanced model prevents the underestimation of the deterministic model caused by using the geometric means of the Hg contents of metal concentrates, and the consideration of the removal compensation effect leads to more accurate estimation of the overall Hg removal efficiency of cascaded APCDs. The Hg emission abatement in the NFMS sector from 2010 to 2017 was evaluated to be 55.6 t, which was 13.5% higher than the estimate without considering the Hg removal compensation effect. The overall uncertainty of the improved model was reduced. This study provides a new methodology for more accurate evaluation of the effectiveness of the national implementation plan for the Minamata Convention on Mercury.

We evaluated mercury (Hg) behavior in a full-scale sewage sludge torrefaction plant with a capacity of 150 wet tons/day, which operates under a nitrogen atmosphere at a temperature range of 250-350 °C. Thermodynamic calculations and monitoring results show that elemental Hg (Hg0) was the dominant species in both the pyrolysis gas during the torrefaction stage and in the flue gas from downstream air pollution control devices. A wet scrubber (WS) effectively removed oxidized Hg from the flue gas and moved Hg to wastewater, and an electrostatic precipitator (ESP) removed significant particulate-bound Hg but showed a limited capacity for overall Hg removal. Hg bound to total suspended solids had a much higher concentration than that of dissolved Hg in wastewater. Total suspended solid removal from wastewater is therefore recommended to reduce Hg discharge. Existing air pollution control devices, which consist of a cyclone, WS, and ESP, are not sufficient for Hg removal due to the poor Hg0 removal performance of the WS and ESP; a further Hg0 removal unit is necessary. A commercial packed tower with sorbent polymer catalyst composite material was effective in removing Hg (83.3%) during sludge torrefaction.

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Coal-derived mercury is the dominant anthropogenic source of mercury emissions. Current sector-specific control may lead to emission leakage via unaccounted cross-sector transfers, particularly during waste treatment. Here, we traced mercury flows across the entire coal-use industrial chain─from production and trade to utilization and waste disposal─offering a comprehensive view of emissions. In 2017, global coal use released 1362 tonnes of mercury, with 705 tonnes emitted into the atmosphere (including 221 tonnes re-emitted from waste disposal), 316 tonnes retained in stock, 275 tonnes stabilized, and the rest discharged into water or soil. Based on the mercury flow, our study identified country-specific key priorities for emission control. Southeast Asian and African nations urgently need advanced end-of-pipe control technologies to reduce emissions. The U.S. (grappling with solid waste stockpiling) and China (facing secondary waste emissions) must improve stabilization methods. Major coal importers like Japan should limit mercury content in imported coal, and countries with strong regulations, such as the EU, must align energy reforms with climate targets. Our study provides a novel, system-wide perspective on mercury pollution throughout the coal life cycle, supporting whole-process control in coal use and the implementation of the Minamata Convention.

As the world's largest energy-related mercury emitter, proper reduction policy is urgently needed in China. However, a quantitative analysis on how different factors affect China's national and regional mercury emissions has been lacking, which hinders the design and implementation of mercury control strategies. To fill the knowledge gap, this study applies a temporal and spatial logarithmic mean divisia index (LMDI) model to reveal the important determinants of mercury emissions across China from 2007 to 2015. The results show a descendant trend generally in energy-related mercury emissions at both national and regional level. Economic scale is the main driving factor while its effect is largely offset by the decreasing mercury emission and energy intensities. However, Jiangsu and Shanxi in 2012-2015 are exceptions with emission growth because of their rebounded emission factors and energy intensities. Moreover, a decoupling effect between energy-related mercury emissions and GDP growth is found, reflecting that there is ongoing green energy transition in China. The spatial decomposition verifies that effects of economic scale and energy intensity are the mainly determinants for mercury emission differences between national average and provincial emissions. Other factors' effects are prominent in several provinces such as Xinjiang, Chongqing and Heilongjiang, where the emission gap is primarily resulted by the differences between national and local mercury intensities. By identifying the determinants of emission changes as well as the differences between the national average and provincial emissions, this study provides insights for formulating more targeted mercury mitigation strategies.

Mercury is a toxic and persistent pollutant that cycles through the atmosphere, hydrosphere, and pedosphere. Understanding temporal trends and driving factors of multimedia mercury emissions is crucial for effective mercury pollution control. This study employed material flow analysis to quantify multimedia mercury emissions─to air, water, and waste─from coal-fired power plants, coal-fired industrial boilers, nonferrous metal smelting, cement production, and municipal solid waste incineration in China during1978-2021. Additionally, the logarithmic mean Divisia index decomposition was used to analyze the drivers of changes in these emissions. Over this period, China's multimedia mercury emissions increased significantly. Mercury entering waste rose from 14.6 to 1662.1 tons, and aquatic releases grew from 0.30 to 31.3 tons. Atmospheric emissions increased from 91.3 tons in 1978 to a peak of 468.9 tons in 2011, before declining to 288.8 tons in 2021. Economic growth dominated multimedia emission increases, whereas structural adjustments partially offset them. End-of-pipe control was the main factor reducing atmospheric mercury emissions and aquatic mercury releases, but it led to the cross-media transfer of mercury to waste. Notably, 80% of multimedia mercury emissions originated from 10% of the total point sources in 2021, highlighting the need for whole-process mercury pollution control targeting key point sources.

Mercury (Hg) emissions from landfill cover soils are an important source of atmospheric Hg affecting local and regional atmospheric Hg budget. To date, soil Hg emissions have been extensively studied, whereas the photoreduction rate of cover soil Hg(II) under various conditions is rarely studied. Herein, two experimental control systems were built to investigate the effect of varying soil Hg(II) concentrations, moistures, and temperature on soil Hg emission in order to obtain the photoreduction rate of soil Hg(II) under varying environmental conditions. The results showed that high soil Hg(II) concentration and high soil temperature can facilitate Hg emission; however, high moisture inhibited Hg emission. In addition, solar radiation is an extremely critical factor for Hg emission and solar radiation-driven photoreduction is an important contribution process for Hg emission; moreover, soil Hg emission is controlled by multiple environmental factors and varies with environmental factors. Through the data fitting and formula calculation, the photoreduction rates under varying conditions are in the range of 1.49-8.54 × 10-10 m2 s-1 W-1, which can be helpful for the construction of a process-based model of soil Hg emission and Hg management in landfills.

Gaseous oxidized mercury (GOM) dry deposition measurements using surrogate surface passive samplers were collected at six sites in the Four Corners area, U.S.A., for the two-year period August, 2017-August, 2019, after the implementation of large power plant mercury emission reductions across the U.S.A. Two-year baseline GOM dry deposition measurements at the same six sites in the Four Corners area, taken before the implementation of U.S.A. power plant mercury control regulations, were conducted earlier from August, 2009-August, 2011. The GOM dry deposition rate estimate decreased at the Four Corners area high elevation remote mountain site of Molas Pass, Colorado (3249 m asl) from 0.4 ng/m2h for August, 2009-August, 2011 to 0.3 ng/m2h for August, 2017-August, 2019. In contrast, GOM dry deposition rate estimates for the remaining five sites increased for August, 2017-August, 2019, ranging from 0.8-1.3 ng/m2h, up from the August, 2009-August, 2011 range of 0.6-1.0 ng/m2h. Comparisons of median GOM dry deposition values showed a statistically significant decrease of 17 ng/m2 at the Molas Pass site between August, 2009-August, 2011 and August, 2017-August, 2019, and a statistically significant increase of 66 ng/m2 and 64 ng/m2, respectively, at the Mesa Verde National Park and Farmington Substation sites between August, 2009-August, 2011 and August, 2017-August, 2019. For the four years of GOM dry deposition data collected in the Four Corners area annual GOM dry deposition levels ranged from 2237 ng/m2yr (at the Molas Pass high elevation remote mountain site) to 11542 ng/m2yr (at the Mesa Verde National Park site), and the estimates were generally higher in magnitude in the spring and summer compared to the fall and winter. In light of the unexpected increases in GOM dry deposition rates at the non-remote sites, it is suggested that large regional wildfires and local anthropogenic mercury emission sources from cities and oil/gas production areas are possible notable contributors to the GOM dry deposition measurements collected in the Four Corners area.

China's energy dependents on coal due to the abundance and low cost of coal. Coal provides a secure and stable energy source in China. Over-dependence on coal results in the emission of Hazardous Trace Elements (HTEs) including selenium (Se), mercury (Hg), lead (Pb), arsenic (As), etc., from Coal-Fired Power Plants (CFPPs), which are the major toxic air pollutants causing widespread concern. For this reason, it is essential to provide a succinct analysis of the main HTEs emission control techniques while concurrently identifying the research prospects framework and specifying future research directions. The study herein reviews various techniques applied in China for the selected HTEs emission control, including the technical, institutional, policy, and regulatory aspects. The specific areas covered in this study include health effects, future coal production and consumption, the current situation of HTEs in Chinese coal, the chemistry of selected HTEs, control techniques, policies, and action plans safeguarding the emission control. The review emphasizes the fact that China must establish and promote efficient and clean ways to utilize coal in order to realize sustainable development. The principal conclusion is that cleaning coal technologies and fuel substitution should be great potential HTEs control technologies in China. Future research should focus on the simultaneous removal of HTEs, PM, SOx, and NOx in the complex flue gas.

Emission limit is a significant index of pollution control in most countries. However, the determination of a reasonable limit value and corresponding supported technical paths is always a challenge during the implementation procedure. In this study, we developed an emission-limit-oriented strategy which links the emission limit with reduction amount via technical paths, so as to control the Hg emissions in the coal-fired power plants in China. Results indicate that tightening the emission limit does not always guarantee the reduction of Hg amounts, especially when coal consumptions keep increasing during the economic growth period. By comprehensively considering the feasibility of different technical paths, the emission limit of 5 μg/m3 is recommended to be executed in 2025. Under the guidance of this limit, the reduction amount of emitted Hg will reach as large as 63 t during 2015-2025 by primarily using multipollutant control measures. During 2025-2030, both alternative energy measures and specific Hg removal measures will be applied to achieve the emission limit of 1 μg/m3 in 2030. The assessment method developed in this study can be used to establish the emission-limit-oriented control strategies in other countries or industries, which will assist the success of the Minamata Convention on Mercury.

The legally binding Minamata Convention was ratified by the Chinese government in 2017, implying that mercury emission mitigation policy design has become an urgent task ever since. As each provincial region has different energy structures and technology levels, their mercury emission profiles may have heterogeneity, thus requiring targeted regional control polices. Therefore, this study investigates the provincial energy-related mercury emissions and identifies their underlying socioeconomic factors during 2007-2012, by combining structural decomposition analysis (SDA) with the multi-regional input-output analysis (MRIO). Results show that the rising consumption per capita and decreasing emission factor are the largest contributors to emission growth and decline, respectively. However, their contributions vary significantly across regions. The rising consumption per capita leads to nearly 20 t emission increase in Shandong and Jiangsu, but less than 1 t in Qinghai. The decreasing emission factor's negative effect on mercury emission reduction is extremely important in Jiangsu, Shandong and Guangdong, but not so obvious in most western provinces. Energy efficiency is another critical contributor to mercury reduction in all provinces except Guizhou, as the coal consumption in Guizhou nearly doubled during 2007-2010. Moreover, production structure and consumption structure have opposite effects during 2007-2010 and 2010-2012: they first drive energy-related mercury emissions growing in most provinces, then inhibit the emissions especially in Shandong and Guangdong. These findings point to targeted mercury mitigation strategies (for example: improving energy efficiency in Guizhou and Liaoning, optimizing economic structure in Henan and Sichuan) for each province.

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The Wuda Coalfield, Inner Mongolia suffers from serious coal fires for more than half a century. Fire-extinguishing projects have been carried out to suppress the coal fires since the last decade, but sporadic surface fires still occur and underground fires are more prevailing. Here, we used a real-time RA-915M Mercury Analyzer with modified inlet to monitor gaseous Hg concentrations in fumes emitted from boreholes that were designed to detect and control the underground coal fires. Meanwhile, offline methods were used to collect the fumes and analyze the contents of the gases including CO, CO2, CH4, C2H6, C2H4 and C2H2. The results showed that gaseous Hg concentrations in fumes from boreholes ranged from 6.42 ± 0.73 to 123.53 ± 34.66 ng m-3, with an average value of 49 ± 44 ng m-3. We suggest that the amounts of coal left for burning or smoldering mainly accounted for the large variation in fume Hg concentrations of underground coal fires. The gaseous Hg concentrations in near-surface air surrounding boreholes varied from 2.38 ± 0.28 to 13.10 ± 0.97 ng m-3, with a mean value of 6.68 ± 3.09 ng m-3. They were higher than the ambient air Hg concentrations measured at a background site near the Yellow River (<2 ng m-3), suggesting underground coal fires were one significant Hg pollution source. Importantly, we found that gaseous Hg concentrations in the boreholes had significantly positive correlations with temperatures and CO (a traditional coal-fire index gas) contents, implying that Hg has the potential to serve as an index gas to monitor the occurrences of underground coal fires in mining goafs.

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China has applied the ultra-low emission technology in coal-fired power plants to control traditional air pollutants and to reduce Hg emissions synergically. In this study, we applied field experiment, model calculation, and literature review to evaluate the Hg control effect of ultra-low emission technology and the potential cross-media effect comprehensively. The dominant ultra-low emission technology significantly improves the atmospheric Hg removal efficiency from 75% to 87%. Such improvement mainly comes from the effect of dust removal devices. Based on the calculated distribution characteristic of Hg content of wastes, we find out that the improvement of Hg control effect of air pollution control devices significantly increase the Hg content of fly ash, which rises from 0.16 mg/kg to 0.33 mg/kg. However, the Hg content of gypsum decreases from 0.75 mg/kg to 0.51 mg/kg. Whether or not to carry out ultra-low emission retrofits, Hg contents of wastes from coal-fired power plants are overall lower than the limit of 25 mg/kg which is intended to be set as the limit for Hg-containing wastes. However, the embodied more than two hundreds of tons Hg in these wastes still require policies to guide the disposal of these wastes.

Controlling anthropogenic mercury emissions is an ongoing effort and the effect of atmospheric mercury mitigation is expected to be impacted by accelerating climate change. The lockdown measures to restrict the spread of Coronavirus Disease 2019 (COVID-19) and the following unfavorable meteorology in Beijing provided a natural experiment to examine how air mercury responds to strict control measures when the climate becomes humid and warm. Based on a high-time resolution emission inventory and generalized additive model, we found that air mercury concentration responded almost linearly to the changes in mercury emissions when excluding the impact of other factors. Existing pollution control and additional lockdown measures reduced mercury emissions by 16.7 and 12.5 kg/d during lockdown, respectively, which correspondingly reduced the concentrations of atmospheric mercury by 0.10 and 0.07 ng/m3. Emission reductions from cement clinker production contributed to the largest decrease in atmospheric mercury, implying potential mitigation effects in this sector since it is currently the number one emitter in China. However, changes in meteorology raised atmospheric mercury by 0.41 ng/m3. The increases in relative humidity (9.5%) and temperature (1.2 °C) significantly offset the effect of emission reduction by 0.17 and 0.09 ng/m3, respectively, which highlights the challenge of air mercury control in humid and warm weather and the significance of understanding mercury behavior in the atmosphere and at atmospheric interfaces, especially the impact from relative humidity.

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ABSTRACT In the past decade, China has motivated proactive emission control measures that have successfully reduced emissions of many air pollutants. For atmospheric mercury, which is a globally transported neurotoxin, much less is known about the long-term changes in its concentrations and anthropogenic emissions in China. In this study, over a decade of continuous observations at four Chinese sites show that gaseous elemental mercury (GEM) concentrations continuously increased until the early 2010s, followed by significant declines at rates of 1.8%–6.1% yr−1 until 2022. The GEM decline from 2013 to 2022 (by 38.6% ± 12.7%) coincided with the decreasing concentrations of criteria air pollutants in China and were larger than those observed elsewhere in the northern hemisphere (5.7%–14.2%). The co-benefits of emission control measures contributed to the reduced anthropogenic Hg emissions and led to the GEM decline in China. We estimated that anthropogenic GEM emissions in China were reduced by 38%–50% (116–151 tons) from 2013 to 2022 using the machine-learning and relationship models.

Coal-fired power plants, as the largest source of human-made mercury emissions, often lack specialized mercury emission control devices. Therefore, developing cost-effective adsorbents and studying their regeneration properties are highly important for mercury removal from flue gas. In this study, the regeneration efficiency and stability of a composite material made from polymetallic Fe/Cu-doped modified biochar combined with the MOF material Cu-BTC were investigated. Based on the analysis of microscopic characteristics, the molecular structure of the regenerated composites was modeled, and the adsorption and regeneration process of Hg0 on their surface was simulated using density functional theory. This helped uncover the underlying mechanisms of mercury removal and regeneration. The results indicate that the optimal regeneration temperature and atmosphere were 350 °C and 5% O2, resulting in the formation of a derived carbon material. The regeneration efficiency reached 92% of that of the original mercury adsorption capacity, and over 80% efficiency was maintained after 10 regeneration cycles. The regenerated samples adsorbed Hg0 through the combined action of surface metal oxides, the metal element Cu, and oxygen-containing functional groups.

China took aggressive air pollution control measures from 2013-2017, leading to the mitigation of atmospheric mercury pollution as a co-benefit. This study is the first to systematically evaluate the effect of five major air pollution control measures in reducing mercury emissions, the total gaseous mercury (TGM) concentration and mercury deposition flux (FLX) for unit emissions reduction. From 2013-2017, China's mercury emissions decreased from 571 to 444 tons, resulting in a 0.29 ng m-3 decrease in the TGM concentration, on average, and in a 17 μg m-2 yr-1 decrease in FLX. Ultra-low emission renovations of coal-fired power plants are identified as the most effective emission abatement measure. As a result of this successful measure, coal-fired power plants are no longer the main mercury emitters. In 2017, the cement clinker sector became the largest emitter due to the use of less effective mercury removal measures. However, in terms of the mitigated TGM concentration and FLX levels per unit emission abatement, newly built wet flue gas desulfurization (WFGD) systems in coal-fired industrial boilers have become particularly effective in decreasing FLX levels. Therefore, to effectively reduce atmospheric mercury pollution in China, prioritizing mercury emissions control of cement clinkers and coal-fired industrial boilers is recommended.

ABSTRACT  Mandatory waste sorting policy in Beijing (2020) lowered mercury inputs to the representative MSWI plant by 67.7 % versus 2019 through removal of batteries and other Hg-rich articles. The front-end change propagated through the entire system, cutting stack emissions 82 % (1.35 ± 0.6 → 0.24 ± 0.05 µg m/³) and decreasing the Hg²⁺ fraction from 45.5 % to 28 %. Higher post-sorting plastic loads elevated chlorine, promoting in-furnace oxidation of Hg0; the resultant Hg²⁺ was efficiently captured by existing wet scrubbing/fabric filters. Mass-balance and speciation data show that source separation functions as a chemical pre-treatment that shifts mercury toward easily removable forms, amplifying downstream control performance without hardware retrofits. Implications: This study provides the first field-scale proof that waste-classification policy can govern mercury emission chemistry. By altering waste composition at the source, mandatory sorting oxidizes elemental mercury and enhances removal efficiency, offering decision-makers a low-cost, proactive tool to meet stringent Hg limits while advancing circular-economy goals.

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Anthropogenic elemental mercury (Hg0) emission is a serious worldwide environmental problem due to the extreme toxicity of the heavy metal to humans, plants and wildlife. Development of an accurate and cheap microsensor based online monitoring system which can be integrated as part of Hg0 removal and control processes in industry is still a major challenge. Here, we demonstrate that forming Au nanospike structures directly onto the electrodes of a quartz crystal microbalance (QCM) using a novel electrochemical route results in a self-regenerating, highly robust, stable, sensitive and selective Hg0 vapor sensor. The data from a 127 day continuous test performed in the presence of volatile organic compounds and high humidity levels, showed that the sensor with an electrodeposted sensitive layer had 260% higher response magnitude, 3.4 times lower detection limit (~22 μg/m3 or ~2.46 ppbv) and higher accuracy (98% Vs 35%) over a Au control based QCM (unmodified) when exposed to a Hg0 vapor concentration of 10.55 mg/m3 at 101°C. Statistical analysis of the long term data showed that the nano-engineered Hg0 sorption sites on the developed Au nanospikes sensitive layer play a critical role in the enhanced sensitivity and selectivity of the developed sensor towards Hg0 vapor.

Coal combustion is a major contributor to environmental pollution, releasing various harmful pollutants, including mercury, which poses significant risks to soil and water quality through atmospheric deposition. For this reason, some countries have established regulatory limits on mercury emissions from coal combustion, requiring the use of advanced pollution control technologies to capture and effectively reduce mercury emission. In this study, the mercury content in coal, coal ash samples and flue gas from the Kolubara A thermal power plant is determined. The results show that the mercury concentration in coal was 0.73 mg/kg, whereas the concentrations in fly ash and bottom ash were 0.02 mg/kg and 0.03 mg/kg, respectively. The mercury concentrations in coal and coal byproducts were in accordance with existing literature. In addition, the overall mercury content in flue gas was 38.73 µg/Nm³, falling within the permissible emission limit for thermal waste treatment in Serbia. The calculated mercury emission factor was below the lower limit specified in the Air Pollutant Emission Inventory Guideline of the European Monitoring and Evaluation of Air Pollutants (EMEP/EEA). These findings provide useful data for long-term environmental monitoring and regulation of mercury emission from coal combustion in Serbia.

ABSTRACT In this study, the mercury (Hg) emission, speciation, and mass distribution of four coal-fired power plants (CFPPs) located at central, southern, and northern Taiwan with various types of air pollution control devices were investigated. Gaseous Hg in the coal-combustion flue gas was sampled by using the Ontario Hydro method, and the solid and liquid samples were collected for understanding the Hg mass balance. The experimental results showed that the total Hg concentrations in flue gases at the inlets of selective catalytic reduction (SCR) varied from 2.984 to 4.692 μg Nm−3, while the total Hg concentrations in the flue gases at the stacks ranged from 0.240 to 0.675 μg Nm−3. These four CFPPs showed similar Hg speciation results at the stacks. The average Hg removal efficiencies of Plants 1 (SCR + electrostatic precipitator [ESP] + wet flue gas desulfurization [WFGD]), 2 (SCR + ESP + WFGD), 3 (SCR + bag filter (BF) + seawater flue gas desulfurization [SWFGD]) and 4 (SCR + BF + SWFGD) were 92.4%, 90.1%, 85.9%, and 84.8%, respectively. Coal was the major raw material in Hg input of CFPPs with a mass flow rate ranging 5.87–12.05 g hr−1. Elemental Hg (Hg0), accounting for 66.4%−97.1% of the total Hg, was the dominant species emitted to the atmosphere. The Hg mass balances for the four CFPPs varied from 86.0% to 117% of the Hg input, suggesting that good mass balances were obtained from the tested CFPPs. Implications: Mercury emissions from coal-fired power plant (CFPPs) have been greatly concerned and should thus be better comprehended. The present study examined the mercury speciation and mass distribution of four CFPPs located at Taiwan. Overall, these CFPPs had similar Hg speciation results at stack and Hg0 was the dominant species emitted to the atmosphere. The selective catalytic reduction (SCR) + electrostatic precipitator (ESP) + wet flue gas desulfurization (WFGD) system had the highest Hg removal efficiency and the Hg mass balances for the four CFPPs varied from 86.0 to 117%. This study helps better understanding the Hg emission inventory of CFPPs and provides useful information for selecting adequate air pollution control devices (APCDs) for Hg control.

Anthropogenic activities, including combustion of fossil fuels, coal, and gold mining, are significant sources of mercury (Hg) emissions into aquatic ecosystems. South Africa is a major contributor to global Hg emissions (46.4 tons Hg in 2018), with coal-fired power stations as the main source. Atmospheric transport of Hg emissions is the dominant cause of contamination, especially in the east coast of southern Africa where the Phongolo River Floodplain (PRF) is located. The PRF is the largest floodplain system in South Africa, with unique wetlands and high biodiversity, and provides essential ecosystem services to local communities who rely on fish as a protein source. We assessed the bioaccumulation of Hg in various biota, the trophic positions and food webs, as well as the biomagnification of Hg through the food webs from the PRF. Elevated Hg concentrations were found in sediments, macroinvertebrates and fish from the main rivers and associated floodplains in the PRF. Mercury biomagnification was observed through the food webs, with the apex predator tigerfish, Hydrocynus vittatus, having the highest Hg concentration. Our study shows that Hg in the PRF is bioavailable, accumulates in biota and biomagnifies in food webs.

Environmental context Mercury (Hg) is a non-essential metal that can accumulate in aquatic biota, including top predators such as elasmobranchs (sharks and rays) and biomagnifying along the trophic web. This study provides data on Hg total, methylmercury (MeHg) and stable isotopes (δ13C and δ15N) for 13 elasmobranch taxa in the Equatorial Western Atlantic Ocean, relating biological and ecological properties with Hg concentrations and the estimated human consumption risk. Rationale Elasmobranchs widely consume fish, making understanding Hg bioaccumulation crucial. Little is known about Hg distribution in their bodies beyond muscle tissue and the associated health risks for both animals and humans who consume them. Methodology This study evaluated Hg, methyl-Hg (MeHg) and stable isotopes (δ13C and δ15N) in the muscle, liver and brain of 13 elasmobranch taxa landed by artisanal fisheries on the Western Equatorial Atlantic Ocean. Results The study revealed that Hg concentrations were highest in muscle tissue, whereas the brain exhibited the greatest percentage of MeHg. Significant correlations between Hg levels and body size, as well as between muscle and brain Hg concentrations, were observed in sharks. Stable isotope values indicated dietary and habitat diversity, and a significant correlation between Hg (log10) and δ15N was found. Mercury concentrations exceeded thresholds for harmful effects in ~76% of the analysed taxa and were also detected in embryos. These taxa also surpassed the local consumption limits, highlighting a potential risk. Discussion The results demonstrated bioaccumulation and biomagnification of Hg in the studied taxa. Muscle Hg was a good predictor of brain Hg levels as a result of the significant correlation between these variables. The high proportion of MeHg in the brain indicates rapid transport of Hg to this organ. Observed Hg concentrations in juveniles and adults may affect their health, whereas concentrations in embryos indicate possible transfer of Hg from the mother to the embryos. This study advises caution when consuming various elasmobranchs, depending on the consumer’s weight and meal frequency.

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The methylated form of mercury, MeHg, is a neurotoxin that bioaccumulates and biomagnifies through aquatic food webs, reaching high concentrations in top trophic species. Many seabird species are wide-ranging and feed on forage fish, so they can be used as sentinel species to assess the level of mercury in pelagic or coastal food webs because they integrate the signal from large areas and from lower trophic levels. The Gulf of Maine provides habitat for many seabirds, including endangered roseate terns (Sterna dougalii), common terns (Sterna hirundo), and the southernmost breeding population of black guillemots (Cepphus grylle). Hg levels were assessed in down of newly hatched chicks of three seabird species to determine pre-hatching Hg exposure. Stable isotopes (δ15N, δ13C) in down and chick contour feathers grown after hatching were used as indicators of adult female diet in the period before laying the egg (down) and pre-fledging chick diet (contour feathers). Black guillemot down THg concentrations were 10.07 ± 2.88 μg/g (mean ± 1SD), 5.5× higher than common tern down (1.82 ± 0.436 μg /g), and 7.4× higher than roseate tern down (1.37 ± 0.518 μg/g). Black guillemots also had higher down feather δ15N values (15.1 ± 0.52 ‰) compared to common (13.0 ± 0.72 ‰) or roseate terns (12.8 ± 0.25 ‰), and in black guillemot down feathers, higher Hg concentrations were correlated with δ15N, an indicator of trophic level. Repeated testing of the same tissue types across multiple years is needed to monitor THg exposure for seabirds in the Gulf of Maine; additionally, monitoring species composition and Hg presence in prey species of the black guillemot population would help to determine the source of high THg concentrations in this species.

Simple Summary Managing aquatic systems is becoming increasingly complex due to human impacts, multiple and competing water needs and climate variability. Considering the Hg concentration present in the top layers of sediment (~20 cm around 30 to 40 years) with the outer layers in the tree cores tree rings cores and in the sediment’s cores from Pacoti estuary and the Ceará estuary, overall data indicate an increase in mercury in recent years. A positive and significant correlation (p < 0.05) was revealed between Hg trends in sediments and Hg trends in annular tree rings. This shared Hg pattern reflects local environmental conditions. The results of this work reinforce the indicators previously described in the semiarid NE region of Brazil, showing that global climate change and some anthropogenic factors are key drivers to Hg exposure and biomagnification for wildlife and humans. Possible climate-induced shifts in these aquatic systems highlight the need for accurate and regionally specific metrics of change in the past in response to climate and for improved understanding of response to climate factors. These processes are inducing a greater mobilization of bioavailable Hg, which could allow an acceleration of the biogeochemical transformation of Hg. Abstract Due to global warming, in the northeastern semiarid coastal regions of Brazil, regional and global drivers are responsible for decreasing continental runoff and increasing estuarine water residence time, which promotes a greater mobilization of bioavailable mercury (Hg) and allows increasing fluxes and/or bioavailability of this toxic trace element and an acceleration of biogeochemical transformation of Hg. In this work, an application of dendrochemistry analysis (annular tree rings analysis) was developed for the reconstruction of the historical pattern of mercury contamination in a contaminated area, quantifying chronological Hg contamination trends in a tropical semiarid ecosystem (Ceará River Estuary, northeastern coast of Brazil) through registration of mercury concentration on growth rings in specimens of Rhizophora mangle L. and using the assessment in sediments as a support for the comparison of profiles of contamination. The comparison with sediments from the same place lends credibility to this type of analysis, as well as the relationship to the historical profile of contamination in the region, when compared with local data about industries and ecological situation of sampling sites. In order to evaluate the consequences of the described increase in Hg bioavailability and bioaccumulation in aquatic biota, and to assess the biological significance of Hg concentrations in sediments to fish and wildlife, muscle and liver from a bioindicator fish species, S. testudineus, were also analyzed. The results of this work reinforce the indicators previously described in the semiarid NE region of Brazil, which showed that global climate change and some anthropogenic factors are key drivers of Hg exposure and biomagnification for wildlife and humans. Considering the Hg concentration present in the top layers of sediment (~20 cm around 15 to 20 years) with the outer layers in the tree ring cores and in the sediment’s cores from Pacoti estuary and the Ceará estuary, overall the data indicate an increase in mercury in recent years in the Hg surface sediments, especially associated with the fine sediment fraction, mainly due to the increased capacity of small particles to adsorb Hg. There was revealed a positive and significant correlation (p < 0.05) between Hg trends in sediments and Hg trends in annular tree rings. This shared Hg pattern reflects local environmental conditions. The Hg concentration values in S. testudineus from both study areas are not restrictive to human consumption, being below the legislated European limit for Hg in foodstuffs. The results from S. testudineus muscles analysis suggest a significant and linear increase in Hg burden with increasing fish length, indicating that the specimens are accumulating Hg as they grow. The results from both rivers show an increase in BSAF with fish growth. The [Hg] liver/[Hg] muscles ratio >1, which indicates that the S. testudineus from both study areas are experiencing an increase in Hg bioavailability. Possible climate-induced shifts in these aquatic systems processes are inducing a greater mobilization of bioavailable Hg, which could allow an acceleration of the biogeochemical transformation of Hg.

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Given their worldwide distribution and toxicity to aquatic organisms, methylmercury (MeHg) and microplastics (MP) are major pollutants in marine ecosystems. Although they commonly co-exist in the ocean, information on their toxicological interactions is limited. Therefore, to understand the toxicological interactions between MeHg and MP (6-μm polystyrene), we investigated the bioaccumulation of MeHg, its cytotoxicity, and transcriptomic modulation in the brackish water flea Diaphanosoma celebensis following single and combined exposure to MeHg and MP. After single exposure to MeHg for 48-h, D. celebensis showed high Hg accumulation (34.83 ± 0.40 μg/g dw biota) and cytotoxicity, which was reduced upon co-exposure to MP. After transcriptomic analysis, 2, 253, and 159 differentially expressed genes were detected in the groups exposed to MP, MeHg, and MeHg+MP, respectively. Genes related to metabolic pathways and the immune system were significantly affected after MeHg exposure, but the effect of MeHg on these pathways was alleviated by MP co-exposure. However, MeHg and MP exhibited synergistic effects on the expression of gene related to DNA replication. These findings suggest that MP can reduce the toxicity of MeHg but that their toxicological interactions differ depending on the molecular pathway.

One of the dangerous heavy metals that can build up in aquatic biota is mercury (Hg). The purpose of this study was to evaluate the environmental health condition in possibly polluted areas near Pelangan Village, Sekotong Subdistrict, West Lombok, and to ascertain the heavy metal level in Gracilaria sp. Using samples taken from Pelangan, Elak-Elak, and Mentigi, the Atomic Absorption Spectrophotometer (AAS) method was used to analyze non-essential heavy metal pollution in Gracilaria sp. According to the findings, Gracilaria samples taken from the Sekotong Subdistrict's coastline area had the greatest levels of mercury pollution, with 0.05 mg/kg in Elak-Elak and 0.14 mg/kg in Pelangan. On the other hand, samples of Gracilaria sp. from the Mentigi coast in North Lombok did not exhibit any mercury contamination (0.00 mg/kg). The levels of mercury accumulation in Gracilaria sp. are classified as dangerous since they surpass the 0.03 mg/kg maximum permissible limit for mercury in consumable products established by the Indonesian National Standard (SNI 7387:2009). Additionally, Gracilaria substrate samples from Pelangan had a mercury contamination level of 0.05 mg/kg, greater than that of Mentigi and Elak-Elak (both at 0.00 mg/kg). The proximate content of Graciaria sp was influenced by the sampling location but was not influenced by mercury contamination.

Mercury (Hg) contamination is a serious environmental problem due to its toxicity and bioaccumulation in aquatic communities. In the Amazon, hydrological fluctuations influence plankton structure and abundance, while gold mining constitutes an important anthropogenic source of Hg, releasing the metal into the water column and facilitating its incorporation by biota. In this study, we assessed total Hg (THg), methylmercury (MeHg), and the MeHg:THg ratio in the planktonic community of the upper Madeira River basin (Brazil) over a 10-year period. Mean concentrations of THg, MeHg, and MeHg:THg were 0.144 ± 0.138 mg kg-1, 0.035 ± 0.049 mg kg-1, and 0.283 ± 0.245, respectively. THg concentrations were higher during the rising-water period, particularly in larger zooplankton, reflecting seasonal hydrological inputs and changes in plankton composition. MeHg concentrations in total plankton were lower during the rising-water period, likely due to dilution effects and reduced bioavailability. When stratified by mesh size, MeHg concentrations were primarily determined by organism size, with larger zooplankton exhibiting higher levels than phytoplankton. The highest MeHg:THg ratios in total plankton and zooplankton were observed during low-water periods, likely driven by lower THg concentrations rather than by increased MeHg production alone. Across all seasons, larger zooplankton consistently exhibited higher MeHg:THg ratios than phytoplankton, indicating size-dependent bioaccumulation patterns. Our results demonstrate that Hg dynamics in plankton are strongly modulated by the hydrological cycle and exacerbated by anthropogenic inputs, emphasizing the importance of long-term monitoring to assess ecological risks in tropical river systems.

Increased lake eutrophication, influenced by changing climate and land use, alters aquatic cycling and bioaccumulation of mercury (Hg). Additionally, seasonally dynamic lake circulation and plankton community composition can confound our ability to predict changes in biological Hg concentrations and sources. To assess temporal variation, we examined seasonal total Hg (THg) and methylmercury (MeHg) concentrations and stable isotope values in seston, waters, sediments, and fish from two adjacent urban eutrophic lakes in Madison, Wisconsin. In Lake Monona, surface sediment THg concentrations were elevated due to comparably higher urbanization and historical industrial inputs, whereas Lake Mendota sediments had lower concentrations corresponding with largely agricultural and suburban surrounding watershed. Surface water THg and MeHg were similar between lakes and seasonally dynamic, but water profiles exhibited elevated concentrations in the meta- and hypolimnia, highlighting water column MeHg production. Seston MeHg concentrations were often highest at shoulder seasons, possibly owing to metalimnetic MeHg delivery, but also differences in biomass and water clarity. The Δ199Hg and δ202Hg values in seston were similar between lakes, despite differing sediment THg concentrations and isotope values, suggesting a shared bioaccumulated source of MeHg. Measurement of MeHg stable isotopes further elucidated that seston and fish predominantly bioaccumulated pelagic-sourced MeHg.

Although estuaries are critical habitats for many aquatic species, the spatial trends of toxic methylmercury (MeHg) in biota from fresh to marine waters are poorly understood. Our objective was to determine if MeHg concentrations in biota changed along a salinity gradient in an estuary. Fourspine Stickleback (Apeltes quadracus), invertebrates (snails, amphipods, and chironomids), sediments, and water were collected from ten sites along the Saint John River estuary, New Brunswick, Canada in 2015 and 2016, with salinities ranging from 0.06 to 6.96. Total mercury (proxy for MeHg) was measured in whole fish and MeHg was measured in a subset of fish, pooled invertebrates, sediments, and water. Stable sulfur (δ34S), carbon (δ13C), and nitrogen (δ15N) isotope values were measured to assess energy sources (S, C) and relative trophic level (N). There were increases in biotic δ13C and δ34S from fresh to more saline sites and these measures were correlated with salinity. Though aqueous MeHg was higher at the freshwater than more saline sites, only chironomid MeHg increased significantly with salinity. In the Saint John River estuary, there was little evidence that MeHg and its associated risks increased along a salinity gradient.

Mercury pollution in aquatic products poses critical risks due to bioaccumulation and biomagnification in the food chain, necessitating tools for rapid, sensitive and accurate detection of mercury in food samples. Herein, we developed a mix-and-read, enzyme-free amplified method for one-pot detection of mercury pollution in aquatic products based on mid-toehold mediated- DNA strand displacement reaction. The key innovation of the method lies in the design of a pre-quenched T-rich duplex probe that enables Hg2+-activated strand displacement through T-Hg2+-T coordination, releasing two fluorophores per binding event to achieve intrinsic signal amplification. This design achieved a detection limit of 4.17 nM with 5.9-fold enhanced sensitivity via the amplification, and allowed to complete Hg2+ quantification within 30 min. Validation in shrimp and salmon yielded 85.70-104.38 % recoveries, shows high accuracy for detecting mercury in food samples. The enzyme-free amplified assay can serve as an efficient tool for monitoring mercury contamination in aquatic products.

Mercury (Hg) is a serious concern for aquatic ecosystems because it may biomagnify to harmful concentrations within food webs and consequently end up in humans that eat fish. However, the trophic transfer of mercury through the aquatic food web may be impacted by several factors related to network complexity and the ecology of the species present. The present study addresses the interplay between trophic ecology and mercury contamination in the fish communities of two lakes in a pollution‐impacted subarctic watercourse, exploring the role of both horizontal (feeding habitat) and vertical (trophic position) food web characteristics as drivers for the Hg contamination in fish. The lakes are located in the upper and lower parts of the watercourse, with the lower site located closer to, and downstream from, the main pollution source. The lakes have complex fish communities dominated by coregonids (polymorphic whitefish and invasive vendace) and several piscivorous species. Analyses of habitat use, stomach contents, and stable isotope signatures (δ15N, δ13C) revealed similar food web structures in the two lakes except for a few differences chiefly related to ecological effects of the invasive vendace. The piscivores had higher Hg concentrations than invertebrate‐feeding fish. Concentrations increased with size and age for the piscivores and vendace, whereas habitat differences were of minor importance. Most fish species showed significant differences in Hg concentrations between the lakes, the highest values typically found in the downstream site where the biomagnification rate also was higher. Mercury levels in piscivorous fish included concentrations that exceed health authorization limits, with possible negative implications for fishing and human consumption. Our findings accentuate the importance of acquiring detailed knowledge of the drivers that can magnify Hg concentrations in fish and how these may vary within and among aquatic systems, to provide a scientific basis for adequate management strategies. Environ Toxicol Chem 2023;42:873–887. © 2023 SETAC

As apex predators, giant otters (Pteronura brasiliensis) are susceptible to the bioaccumulation of heavy metals, particularly in regions where gold-mining contributes to mercury (Hg) pollution. This is the broadest-scale study assessing Hg and selenium (Se) concentrations in the Pantanal. Samples from 10 sites across the Pantanal were analysed using inductively coupled plasma mass spectrometry. We constructed a two-factor generalized additive model (GAM) to investigate the relationship between Hg concentrations in giant otters and their location along river courses in gold-mining areas. To determine the feasibility of merging the dataset from the present study with the dataset of a previous study carried out by our group during 2016–2017, we included the datasets as a factor in the analysis. The GAM results supported the feasibility of merging the datasets. Additionally, we measured Se concentrations due to their potential to mitigate Hg toxicity. Higher Hg levels were found in otters from watercourses near gold-mining areas, with concentrations decreasing downstream, revealing a contamination gradient and the extensive impact of local pollution on wetlands. The highest Hg concentration was recorded in the Bento Gomes River, within a gold-mining area, whereas otters from unconnected sites exhibited lower Hg levels.

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The increasing frequency and severity of wildfires are among the most visible impacts of climate change. However, the effects of wildfires on mercury (Hg) transformations and bioaccumulation in stream ecosystems are poorly understood. We sampled soils, water, sediment, in-stream leaf litter, periphyton, and aquatic invertebrates in 36 burned (one-year post fire) and 21 reference headwater streams across the northwestern U.S. to evaluate the effects of wildfire occurrence and severity on total Hg (THg) and methylmercury (MeHg) transport and bioaccumulation. Suspended particulate THg and MeHg concentrations were 89 and 178% greater in burned watersheds compared to unburned watersheds and increased with burn severity, likely associated with increased soil erosion. Concentrations of filter-passing THg were similar in burned and unburned watersheds, but filter-passing MeHg was 51% greater in burned watersheds, and suspended particles in burned watersheds were enriched in MeHg but not THg, suggesting higher MeHg production in burned watersheds. Among invertebrates, MeHg in grazers, filter-feeders, and collectors was 33, 48, and 251% greater in burned watersheds, respectively, but did not differ in shredders or predators. Thus, increasing wildfire frequency and severity may yield increased MeHg production, mobilization, and bioaccumulation in headwaters and increased transport of particulate THg and MeHg to downstream environments.

Background: Pollution of aquatic environments with heavy metals causes severe adverse effects on fish, invertebrates, and human. The importance of this study lies in the fact that long-term ingestion of heavy metal-contaminated fish can result in the accumulation of harmful metals in numerous organs and pose a major risk to human health. Aim: The current study was designed to investigate the concentrations of toxic arsenic (As), lead (Pb), and mercury (Hg) in the liver, gills, and muscles of highly consumed aqua cultured common carp (Cyprinus carpio L.) in Baqubah city, to evaluate the toxicopathological bioaccumulation of As, Pb, and Hg in consumed fish and the potential human health risk after consumption and give clear indication for a status of heavy metal contamination for water used in aquaculture of common carp (C. carpio L.). Methods: A total of 10 Fresh fish of common carp (C. carpio L.) were randomly selected from local Baqubah markets/Diyala province/Iraq in different interval from September 2022 to January 2023. The source of fish in Baqubah’s local markets is fish aquacultured in earthen ponds as well as cages in the Tigris River in Diyala province. Flame atomic absorption spectrometer was used to estimate the level of As, Pb, and Hg in liver, gills, and muscles of collected fish. Histopathological sections were prepared for evaluation of toxic pathological effects of metals on C. carpio organs. Results: Bioaccumulation of arsenic and lead in liver, gill, and muscle samples was within and less than the permissible limit set by WHO while the bioaccumulation of mercury exceeds the permissible limits set by WHO. Histopathological findings of the gill section showed telangictatisis and epithelial lifting in secondary lamellae with hemorrhage and blood congestion and central venous dilation and epithelium hyperplasia with complete fusion of the secondary lamellae and edema in the filamentary epithelium in addition to mononuclear cells infiltration. Histopathological findings of liver revealed degenerative and necrotic changes in liver tissue distinguished by pyknosis with the existence of necrosis in cells and dilation of the sinusoids with cytoplasmic vacuolation. Conclusion: The bioaccumulation of mercury is higher than permitted levels in common carp (C. carpio) which indicates high contamination level of main sources for fresh waters in Diyala province mainly from Diyala and Tigris rivers.

The present study investigates the bioaccumulation of heavy metals and associated histopathological alterations in Clarias batrachus (walking catfish) from selected aquatic ecosystems in Durg District, Chhattisgarh. This region, characterized by increasing industrial and agricultural activities, presents potential sources of metal contamination in freshwater bodies. Water, sediment, and fish samples were collected from three sites (high, moderate, and low contamination zones) and analyzed for cadmium (Cd), lead (Pb), mercury (Hg), chromium (Cr), and zinc (Zn) using Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Tissues (gills, liver, kidney, and muscle) of fish were examined for bioaccumulated metals and subjected to histopathological analysis. Results indicated significant bioaccumulation, particularly in metabolically active tissues such as the liver and kidneys. Correlation analysis revealed strong positive relationships between metal concentrations and lesion severity, with Hg and Cd showing the highest correlation in liver and gill tissues, respectively. Histopathological findings included epithelial lifting, lamellar necrosis, hepatocyte vacuolation, and tubular degeneration. Principal Component Analysis (PCA) highlighted the clustering of specific metals with organ-specific damage, while ANOVA confirmed significant differences in lesion severity across sites. This study affirms Clarias batrachus as an effective bioindicator and highlights histopathological biomarkers as sensitive tools for early detection of aquatic toxicity. The findings underscore the ecological risk posed by heavy metal pollution and stress the need for regulatory intervention, routine monitoring, and ecotoxicological assessments to safeguard both aquatic biodiversity and public health in Chhattisgarh and similar regions.

Mercury (Hg) is a potent neurotoxicant and poses a risk to human health through the ingestion of Hg-contaminated fish. Mercury, especially in its organic form methylmercury (MeHg), biomagnifies up food chains such that even small aqueous concentrations of Hg can result in significant concentrations of total Hg in fish. Understanding the ecological and human health risks associated with Hg and MeHg exposure requires an understanding of the factors that affect its bioaccumulation in aquatic species. We compiled estimates of three biokinetic parameters: uptake rate (ku), assimilation efficiency (AE), and efflux rate (ke). These parameters describe contaminant uptake from aqueous (ku) and dietary (AE) exposure and the rate of excretion (ke). We found parameter values for 38 and 34 different species of fish and aquatic invertebrates, respectively, and collected 502 parameter values in total. We used a machine learning technique to establish the relationships between experimental and physiological variables and these parameter values. We found differences in which variables were associated with biokinetic parameter values for fish and aquatic invertebrates. The form of Hg was the most impactful variable, influencing values of all parameters except ku for invertebrates, for which aqueous exposure time was the only significant predicator variable. The parameter ke were the only values significantly influenced by more than one variable, with water type (freshwater, brackish, or marine), organism weight, and form of Hg significantly impacting parameter values for fish and/or invertebrates. To our knowledge, this study represents the most extensive review of biokinetic parameters of Hg and MeHg accumulation in aquatic organisms. Environmental parameters found to significantly impact Hg and MeHg bioaccumulation in past studies were not identified as important in our analyses across aquatic ecosystems and species. Our dataset and analysis reveal novel patterns that may help us better understand and manage Hg bioaccumulation.

This study evaluated -for the first time- the occurrence and distribution of total Hg in abiotic (dissolved and particulate water fractions) and biotic (gills and muscle tissues of six commercial fish species) compartments within a South American coastal environment with anthropogenic pressure. This study dealt with environmental issues on developing countries which, as they are in continuous growth, face the highest rate of coastal transformation. Total Hg content was determined by acid digestion and measured using a cold vapor atomic absorption spectrophotometer. Results revealed that dissolved Hg exceeded the recommended levels for superficial saline waters in 67% of the cases. Hg concentrations varied among fish species and its tissues. The results suggested that metal burden in fishes achieved a mean maximum accumulation towards the muscle, with concentrations below the international maximum permitted values. The estimated daily intakes calculated suggest that people would not experience significant health risks through fish consumption.

In the natural ecosystem, aquatic organisms are exposed to a cocktail of chemicals that may result in toxicological responses differing from those of individual chemicals. In the present study, mussels were exposed using a semi-static and triplicated design to either control (no added metal), 50 µg l-1 (Hg alone), 50 µg l-1 (Cd alone), or 50 µg l-1 Hg plus 50 µg l-1 Cd (Hg + Cd) mixture for 14 days. Tissues were collected on days 0, 2, 4, 8, and 14 for metal analysis and sub-lethal responses using a suite of assays. Tissue metal concentrations were not significantly different in the single metal (Hg or Cd) compared to the Hg plus Cd mixture treatment for all tissues, apart from the gill of the Cd alone treatment. At the end of the experiment, the gill Cd concentration was significantly increased in the Hg plus Cd mixture compared to the Cd alone treatment, suggesting the influence of Hg on Cd uptake. The percentage increases of the Hg plus Cd mixture compared to the arithmetic sum of the individual metals were ( %): 20.2, 9.3, 25.1, 23.8, 10.7, and 12.4 for adductor muscle, digestive gland, gill, gonad, remaining soft tissue, and haemolymph, respectively. There were no observed treatment effects on total haemocyte count, haemolymph protein, or glucose concentration in the cell-free haemolymph. Neither was there any treatment effect on osmotic pressure, ions in the tissues, or in the cell-free haemolymph. At the end of the experiment, Hg-mediated oxidative damage, as an increase of thiobarbituric reactive substances (TBARS) and apparent depletion of total glutathione. This was observed in the gill and digestive gland of the Hg alone and Hg plus Cd mixture. Histopathology examination showed similar pathology in the Hg alone and the Hg plus Cd treatment. In conclusion, despite some oxidative stress and pathology during metal exposure, the accumulation of metals and effects on mussel health were similar between single exposures and a mixture of Hg plus Cd. In terms of risk assessment, regulations for the individual metals should suffice to protect against the mixture of Hg plus Cd, at least for adult M. edulis in full-strength seawater.

Mercury (Hg) in high exposures can be a potent life threatening heavy metal that bioaccumulate in aquatic food-chain mainly as organic methylmercury (MeHg). In this regard, fish and seafood consumptions could be the primary sources of MeHg exposure for human and fish-eating animals. The objective of the present study was to elucidate the effects of dietary supplementation of some antioxidants on induced mercury toxicity in mice model. In this study, a 30-day long investigation has been conducted to evaluate the dietary effect of selenium (Se) in combination with vitamin C and vitamin E on methylmercury induced toxicity in mice. Total 54 mice fed the diets with three levels of Hg (0, 50 or 500 μg kg-1) and two levels of Se in combination with vitamin C and E (Se: 0, 2 mg kg-1; vitamin C: 0, 400 mg kg-1; vitamin E: 0, 200 mg kg-1) in triplicates. The results show that Hg accumulated in blood and different tissues such as muscle, liver and kidney tissues of mice on dose dependent manner. The bioaccumulation pattern of dietary Hg, in decreasing order, kidney > liver > muscle > blood. Superoxide dismutase levels in blood serum showed no significant differences in mice fed the diets. However, dietary antioxidants significantly reduced the levels of thiobarbituric acid reactive substances in mice fed the mercury containing diets. Cytochrome c oxidase enzyme activities showed no significant differences as the mercury level increases in liver and kidney tissues of mice. Kaplan-Meier curve showed a dose- and time-dependent survivability of mice. Cumulative survival rate of Hg intoxicated mice fed the antioxidant supplemented diets were increased during the experimental period. Overall, the results showed that dietary Se, vitamin C and vitamin E had no effect on reducing the mercury bioaccumulation in tissues but reduced the serum lipid peroxidation as well as prolonged the cumulative survival rate in terms of high Hg exposures in mice.

Mercury distribution and bioaccumulation in aquatic ecosystems of tropical Australia is poorly characterised. Barramundi (Lates calcarifer), a widespread high-order predator in both fresh and coastal marine waters of the region, fulfils requirements for a bio-indicator of mercury contamination. In a study of the Mary River system of the Northern Territory, total mercury in the muscle tissue of 300 specimens gathered over four years (2013-2017, across both wet and dry seasons) was determined by direct combustion-atomic absorption spectrometry. Source of nutrition and trophic position of barramundi in the food web was also estimated via carbon and nitrogen isotopes (δ13C and δ15N), respectively, in tissue by stable isotope mass spectrometry, and determination of strontium isotopes (87Sr/86Sr) in otoliths by laser ablation-ICPMS differentiated between freshwater and saltwater residence. Results showed that fish moving into freshwater floodplain wetlands concentrated mercury in muscle tissue at approximately twice the level of those that remained in saline habitats. Resolving life histories through otolith analyses demonstrated diversity in mercury bioaccumulation for individual fish of the same migratory contingent on the floodplains. Although trophic level (δ15N), capture location, source of nutrition (δ13C), and age or size partly predicted mercury concentrations in barramundi, our results suggest that individual variability in diets, migration patterns and potentially metabolism are also influential. Using a migratory fish as a bio-indicator, and tracking its life history and use of resources, proved valuable as a tool to discern hot spots in a coastal waterway for a contaminant, such as mercury.

Sediments represent the main reservoir of mercury (Hg) in aquatic environments and may act as a source of Hg to aquatic food webs. Yet, accumulation routes of Hg from the sediment to benthic organisms are poorly constrained. We studied the bioaccumulation of inorganic and methylmercury (HgII and MeHg, respectively) from different geochemical pools of Hg into four groups of benthic invertebrates (amphipods, polychaetes, chironomids, and bivalves). The study was conducted using mesocosm experiments entailing the use of multiple isotopically enriched Hg tracers and simulation of estuarine systems with brackish water and sediment. We applied different loading regimes of nutrients and terrestrial organic matter and showed that the vertical localization and the chemical speciation of HgII and MeHg in the sediment, in combination with the diet composition of the invertebrates, consistently controlled the bioaccumulation of HgII and MeHg into the benthic organisms. Our results suggest a direct link between the concentration of MeHg in the pelagic planktonic food web and the concentration of MeHg in benthic amphipods and, to some extent, in bivalves. In contrast, the quantity of MeHg in benthic chironomids and polychaetes seems to be driven by MeHg accumulation via the benthic food web. Accounting for these geochemical and dietary drivers of Hg bioaccumulation in benthic invertebrates will be important to understand and predict Hg transfer between the benthic and the pelagic food web, under current and future environmental scenarios.

Riverine sediments are important sites of mercury methylation and benthic invertebrates may be indicators of Hg exposure to higher organisms. From 2014 to 2018, sediments and invertebrates were collected along a mercury gradient in the Toce River (Northern Italy) and analyzed for THg and MeHg. Concentrations in invertebrates, separated according to taxon and to Functional Feeding Group, ranged from 20 to 253 µg kg−1 dry weight (d.w.) for THg, increasing from grazers (Leuctra, Baetis, Serratella) to predators (Perla). MeHg ranged from 3 to 88 µg kg−1 d.w. in biota, representing 6–53% of THg, while in sediments it was mostly below LOD (0.7 µg kg−1), accounting for ≤3.8% of THg. The Biota-Sediment Accumulation Factor (BSAF, ranging 0.2–4.6) showed an inverse relation to exposure concentrations (THg in sediments, ranging 0.014–0.403 µg kg−1 d.w.) and to organic carbon. THg in invertebrates (up to 73 µg kg−1 wet weight), i.e., at the basal levels of the aquatic trophic chain, exceeded the European Environmental Quality Standard for biota (20 µg kg−1 w.w.), posing potential risks for top predators. Concentrations in adult insects were close to those in aquatic stages, proving active mercury transfer even to terrestrial food chains.

The bioaccumulation of mercury (Hg) and polyunsaturated fatty acids (PUFA) in zoobenthos varies across aquatic food webs. In this field study, contents of total Hg (THg), methylmercury (MeHg) and PUFA were investigated in zoobenthos of Chinese reservoirs and Swedish lakes, with contrasting environmental characteristics and algal diet sources, which can result in difference of Hg and PUFA in zoobenthos from these two habits. Using PUFA as dietary biomarkers of algae in zoobenthos, we evaluated effects of environmental factors and algal diet sources on the accumulation of THg, MeHg, and the highly required PUFA eicosapentaenoic (EPA, 20: 5n-3) and docosahexaenoic acid (DHA, 22:6n-3) in zoobenthos. Average THg and MeHg in zoobenthos were higher in Chinese reservoirs than Swedish lakes (p < 0.05). Average EPA content of zoobenthos was similar in these two habitats (p > 0.05), yet average DHA content of zoobenthos was higher in Chinese reservoirs than Swedish lakes (p < 0.05). Total Hg and MeHg contents of zoobenthos in Swedish lakes were predicted by environmental factors; e.g., negatively with pH and positively with dissolved organic carbon (DOC) concentrations, yet had no significant relationship with the algal dietary. In Chinese reservoirs, however, no environmental factor correlated well with THg contents in zoobenthos, and only DOC concentrations showed positive correlation with MeHg contents in zoobenthos. Besides, the algal dietary was also positively correlated with MeHg contents in zoobenthos. EPA and DHA contents of zoobenthos in Swedish lakes primarily associated with algal diet. By contrast, in Chinese reservoirs, EPA and DHA contents of zoobenthos were affected by both environmental factors and algal diet.

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A model capable to estimate the mercury (Hg) removal efficiency in the fabric filter of a real Waste-to-Energy plant with dynamic operating conditions has been developed. The mathematical model is based on Langmuir equation and Hg mass balance on mercury, in both gaseous and adsorbed phases, along the growing filter cake and inside the activated carbon particles. The activated carbon properties and the Langmuir isotherm parameters have been obtained by fitting the model to real plant data, characterized by variable mercury inlet concentrations. The model is then validated on another dataset coming from the same plant. The obtained Hg removal efficiency falls within ± 3 % error band and with a mean absolute percentage error equal to 0.87 %. The model is suitable for the development of a data-driven activated carbon feed control strategy to increase the economic and environmental sustainability of the WtE plants as well as in the development of virtual sensors to use as a replacement when the continuous stack mercury monitors fail.

Detrimental effects of mercury (Hg) on ecosystems and human health have been well-documented. Whereas emissions of gaseous elemental mercury (GEM) from e-waste recycling have been reported in developed countries, much less is known about the situation in the Global South. Using a total of 132 passive air samplers, seasonally resolved concentrations of GEM in air were measured continuously at 32 informal e-waste recycling facilities and background location in Pakistan for a period of one year between September 2020 and December 2021. Annual average GEM concentrations at the studied locations ranged from 1.8 to 92 ng m-3. Among the studied cities, higher concentrations were measured in Karachi (mean ± s.d: 17 ± 22, range: 4.2-92 ng m-3), Lahore (16 ± 4.2, 8.2-22 ng m-3) and Peshawar (15 ± 17, 4.9-80 ng m-3), while lower levels were measured in Hyderabad (6.9 ± 6.2, 3.1-25 ng m-3), consistent with a higher rate of informal recycling activities in metropolitan areas. Seasonally, higher GEM levels occurred during autumn (15 ± 16: 3.3-92 ng m-3) and summer (13 ± 8.7: 1.8-80 ng m-3) than in winter (12 ± 8.4: 2.5-49 ng m-3) and spring (9.2 ± 7.3: 1.8-80 ng m-3), possibly reflecting enhanced volatilization at higher temperatures and/or varying magnitude of recycling operations in different seasons. Policies and strict regulations related to e-waste management should be developed and implemented urgently in the country.

A novel biochar involving pyrolysis of dewatered algal waste combined with KOH and residual FeCl3 co-activation was synthesized as an efficient sorbent specifically for Hg0 removal from coal-fired flue gas. It was found that the SBET of biochar co-activated by KOH and FeCl3 (BCFK) was 195.82 m2 g-1, much higher than that of single FeCl3 activated biochar (BCF) of 133.38 m2 g-1 and un-activated biochar (UBC) of 20.36 m2 g-1. Furthermore, BCFK exhibited higher magnetization characteristics as well as elemental Fe and Cl contents of 2.71% and 10.33%, respectively, based on the combined characterization of XPS and VSM, etc., which is a jump of about 10-fold compared to BCF. This allows BCFK to show the best Hg0 removal capability of 689.66 μg g-1 under the inlet Hg0 concentration of 100 μg m-3 and 150 °C, according to pseudo-second-order kinetic model. Further analysis by XPS and Hg-TPD (Temperature Programmed Desorption) revealed that oxidation by Cl∗ radicals and C-Cl as well as weak chemisorption contributed to the removal of Hg0. Eventually, this efficient, simply prepared, low-cost and easily separable biochar distinguished itself in comparison to other materials. This will undoubtedly promote the valorization of algae and provide a reliable alternative material for the treatment of coal-fired flue gas.

Landfills harbor ideal conditions for microbial mercury methylation. However, the levels and distribution of mercury (Hg) and methylmercury (MeHg), potential microbial Hg methylation, and their linkage within landfills are largely unknown. In the present study, total mercury (THg), MeHg, the Hg methylation gene (hgcA) and mer operon were quantified in 30 waste samples from different depths (0-30 m) at 5 locations within a large-scale landfill in China. The average concentrations of THg and MeHg in the solid waste samples were 1422.91 ng/g and 3.15 ng/g, respectively. THg (up to 14405.29 ng/g) and MeHg (up to 10.42 ng/g) have high concentrations in the middle part (10-15 m) along the depth profiles. The concentration of THg was strongly positively (both p < 0.05) correlated with the MeHg concentration and the relative abundance of hgcA, indicating that the THg concentration can play an important role in microbial Hg methylation. The hgcA genes were detected in most samples and mer operon were detected in all samples. Combined hgcA qPCR and metagenomics data showed that Archaea Methanofollis may mainly account for Hg methylation within landfills. These findings provide fundamental knowledge on Hg cycles in landfills.

Small incinerators of dangerous wastes, including those from hospitals, are a source of emissions of highly variable compositions and concentrations. Mercury is a very dangerous pollutant causing neurotoxicity in human organism. The effect of HCl concentration on adsorption of mercury on activated carbon-based sorbent was studied for the incineration of hospital waste in a 250 kg/h capacity unit. The maximum concentration of adsorbed mercury on activated carbon was determined as a function of concentration of Hg and HCl in combustion products. Based on the expected chemical reactions and the thermodynamics, the adsorption of mercury from flue gases in oxidising atmosphere has been explained. The activated carbon-based sorbent was also capable of adsorbing acid gases like HCl. The efficiency of removal of mercury from combustion products increased up to 85-87% with the concentration of HCl in flue gases. The addition of calcium hydroxide increased the amount of mercury trapped on the sorbent only by about 10%. These tests proved that an entrained flow adsorber is a suitable unit for the removal of mercury from combustion products. The consumption of activated carbon for the mercury removal was from 0.1 to 0.15 mg/Nm3 of flue gas. The advantage of an entrained flow adsorber lies in its easy continuous operation. Therefore, it is a suitable unit for small and medium size incinerators of municipal and hospital waste.

Modeling approaches are generally used to describe mercury transformations in a single step of flue gas treatment processes. However, less attention has been given to the interactions between the different process stages. Accordingly, the mercury removal performance of a full-scale solid waste incineration plant, equipped with a dry flue gas treatment line was investigated using two complementary modeling strategies: a thermochemical equilibrium approach to study the mercury transformation mechanisms and speciation in the flue gas, and a kinetic approach to describe the mercury adsorption process. The modeling observations were then compared to real-operation full-scale data. Considering the typical flue gas composition of waste incineration facilities (high concentrations of HCl compared to Hg), it was found that a process temperature decrease results in better mercury removal efficiencies, associated with a higher oxidation extent of Hg in HgCl2, and the enhancement of the sorbent capacity. Improvements can also be attained by increasing the sorbent injection rate to the process, or the solid/gas separation cycles. An empirical correlation to predict the mercury removal efficiency from the main operating parameters of dry flue gas treatment units was proposed, representing a useful tool for waste incineration facilities. The presented modeling approach proved to be suitable to evaluate the behavior of full-scale gas treatment units, and properly select the most adequate adjustments in operating parameters, in order to respect the increasingly constraining mercury emissions regulations.

This study describes the main mechanisms that take part in the mercury homogeneous oxidation pathway in presence of some of the main reactive compounds formed during waste incineration processes (O2, HCl, SO2 and NO). Series of model, synthetic dry flue gases were used to elucidate the effects of HCl, SO2, NO and their proportions in the gas on mercury behaviour. Three samples of fly ash collected from a MSWI facility were characterized and evaluated both for Hg heterogeneous oxidation and Hg removal in a laboratory scale device. The results obtained in this study showed that homogeneous mercury oxidation in the models MSWI and coal combustion flue gas atmospheres was 52 ± 5% and 25%, respectively. SO2, NO and HCl have a synergetic effect in Hg oxidation in presence of oxygen, but the main differences found are mainly caused by the strong influence of HCl and the likely inhibitory oxidation effects of SO2. Surface area together with carbon and chloride content of the fly ashes were correlated with their capacity for Hg-heterogeneous oxidation and adsorption. The sample of fly ash with relatively high content of unburnt carbon and chlorine, and with BET surface (2.42 m2/g) was able to remove up to 100% of Hg0 (g) during 300 min. The results obtained in this study provide a complete overview of the behaviour of mercury during MSWI processes and may help to clarify the fate/behaviour of mercury in a filter (e.g. electrostatic precipitator) providing a deeper knowledge about the impacts of fly ash properties on mercury fate in waste incineration.

The principle of recycling materials has been adopted as part of the cement industry's contribution to the transition from linear to circular economy. This study examines mercury flow in a cement plant and investigates the impact of circular economy policies on mercury emissions. The raw material analysis indicate that steel industry sludge is the main mercury source (40.9 %), followed by limestone (23.0 %) and silica sand (13.4 %). Recycled materials, with a mercury content of 0.267 mg/kg, contribute more mercury than raw materials (0.065 mg/kg). The intermediates in the production process enrich mercury, with raw mill fly ash containing 19.7 mg/kg. Mercury output is primarily via flue gas (98.8 %), with a mass flow rate of 16.34 g/hr, while clinker accounts for only 1.1 %. The emission factor from the raw mill stack is 165 mg Hg/ton clinker, higher than those reported in previous studies. The mass balance is 130 %, within the acceptable range (70-130 %). While adopting circular economy policy is beneficial for waste management, it increases overall mercury emission from cement plants, necessitating improved recycled material quality and air pollution control measures.

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There is a crucial need to understand the outlook for changes in mercury supply and demand in response to the 2017 entry into force of the Minamata Convention on Mercury. If demand exceeds supply there will be a shortage, but if supply exceeds demand there will be excess mercury, and ultimately the need to prepare for the final disposal of elemental mercury. This study estimates global mercury supply and demand from 2010 to 2050, by region, and projects excess mercury based on recent trends and consideration of impacts of the Convention. The analysis notes a downward trend in both supply and demand, but the supply of mercury from primary mining has not decreased as much as initially expected, while mercury recovery from by-products of nonferrous production has not yet been implemented extensively. Under a business-as-usual projection, there is excess supply until a shortage appears around 2030, but a surplus returns after 2035, and there is a projected excess supply of 59 tons annually in 2050. Relying on the level of mercury recovery in the nonferrous sector, global cumulative stock of excess mercury is projected at 14,439–20,943 tons in 2050.

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The environmental risk assessment and the factors influencing heavy metals (HM) in the soil at the municipal solid waste landfill sites (MSWLs) were studied by literature review, field survey, and statistical methods. The results indicated that the dominant HM contamination in the soil at the MSWLs was caused by chromium (Cr) with the Nemero index values (PI) from 22.7 to 44.3 and zinc (Zn) with the PI from 0.7 to 9.8. There were significant differences in the Cr, mercury (Hg), lead (Pb), Zn, and arsenic (As) concentrations between soil samples from sanitary and non-sanitary landfills (NSLs) where HM contamination (PI = 10.9) was more obvious. As (CRAAs = 2.35 × 10-4) and cadmium (Cd) (CRACd = 1.45 × 10-4) posed potential carcinogenic health effects. The soil Cd concentration had a significant negative correlation (r = -0.476**) with the landfill age. The soil As concentration had a significant positive correlation (r = 0.472**) with rainfall in NSLs. There were significant differences in the As (P = 0.042) and copper (Cu) (P = 0.042) concentrations between soil samples from the surrounding areas of MSWLs and the base where soil had higher HM concentrations. For the efficient prevention of HM ecological risk, a scientific site selection, undamaged coverage and anti-seepage systems, standardized management, and ongoing monitoring are required.

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The progressive decarbonisation of industry is leading to a reduction in coal consumption and the substitution for coal with other types of fuels, including waste-derived alternative fuels. These fuels are characterised by high variation in the content of highly toxic mercury. Co-combustion with coal can cause significant emissions, exceeding mercury emission limits. Various alternative fuels (refuse-derived fuel (RDF), waste paper, textiles, plastics, film, tires and their char, and sewage sludge) were examined for mercury content. The mercury content in analysed alternative fuels ranged from 0.4 to 92.0 µg Hg/MJ, with an average of 17.7 µg Hg/MJ. The fuels with the highest mercury content were RDFs (2.0-79.3 µg Hg/MJ) and sewage sludge (42.3-92.0 µg Hg/MJ). An acceptable amount of RDF added to hard coal which would remain within the emission limits was estimated to be 9-24% of the chemical energy in the blend. For sewage sludge, this amount was estimated to be 5-13%. For brown coal, with a much higher mercury content than hard coal, co-combustion with alternative fuels has a positive effect on reducing mercury emissions. It is possible to meet the mercury emission limits with a 95% contribution of the chemical energy coming from RDF. The blending of various types of waste supported by mild pyrolysis of high-mercury waste allows alternative fuels with relatively low mercury content to be produced. Such fuels may contribute a reduction in mercury emissions from coal-fired power plants in Poland.

Heavy metals in leachate during food waste composting may produce different degrees of pollution hazards and further induce environment costs, when the concentrations of heavy metals exceed the discharging quality standards. Quantitative evaluation of heavy metals' pollution hazards and estimation of such environmental costs are under-represented in the existing literature. This paper uses a logistic function approach to evaluate the extent of pollution hazards of heavy metals such as cadmium (Cd), chromium (Cr), mercury (Hg), lead (Pb) and arsenic (As) and to estimate heavy metals' environmental costs in leachate during food waste composting from Minhang food waste treatment plant located in northern Shanghai, China. Major findings of this study are: (1) The pollution hazards rate of Cd amounts to 94.03%, probably because Cd-containing materials such as plastics are mixed with food waste; (2) With the comprehensive pollution hazards rate estimated as 94.48%, the environmental costs caused by heavy metals in leachate during food waste composting amount to US$0.52 per tonne. This magnitude of environmental costs is meaningful and significant, considering that it is equivalent to 2.97% of Shanghai's food waste treatment charges.

In 1989, the two major sources of mercury emissions to the atmosphere in the U.S. were coal-fired power plants (80 tons Hg) and waste to energy power plants (82 tons Hg). This paper examines what has happened to these two major sources of mercury emissions since 1989. A comparison within the waste management industry is, also, provided. The 2014 total anthropogenic emissions of mercury in the U.S. were 51.8 t. The results of the analysis of emissions by industrial sector showed that the largest source of anthropogenic mercury were coal-fired power plants. Among industrial processes, the ferrous metals recycling and the cement industries were the largest emitters of mercury. With regard to waste-to-energy power plants, all of which, since the nineties, have installed advanced emission control systems, the results have been very satisfactory: The authors obtained mercury emission data from operators of most of the waste-to-energy (WTE) power plants in the US. The results showed that in 2014 the 77 U.S. WTE plants in total emitted 0.4 tons of mercury, corresponding to 0.77% of the U.S. total. This number was one half of that reported by the National Emissions Inventory (NEI) for "municipal waste combustion'' (0.64 t) due to the fact that the NEI survey included incinerators without energy recovery. A 2002 Earth Engineering Center study had shown that the mercury emissions of the U.S. WTE industry decreased from 81.8 t in 1989 to 2.2 t in 2001. The present study showed that between 2001 and 2014 the U.S. WTE industry mercury emissions were reduced further, by a factor of seven.

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One of the main issues in the fluorescent lamp recycling sector is the mercury contamination of output fractions and occupational exposure associated with recycling operations. The aim of this study is to carry out effective mercury mass balance determinations and improve mercury recovery by finding the optimal levels for the recycling process parameters. These optimizations will allow upstream mercury emissions to be reduced, which will help to avoid mercury exposure among WEEE recycling workers. Firstly, the distribution of mercury was assessed in new and spent lamps. For new fluorescent tubes, the mean percentage of mercury in the solid phase is lower in new fluorescent tubes (19.5% with 5.5% in glass, 9.7% in end caps and 4.3% in luminescent powder) than in spent tubes (33.3% with 8.3% in glass, 12.9% in end caps and 12.1% in luminescent powder). The parametric study also shows that the finer the grains of glass, the higher the concentration of mercury (1.2 µg Hg/g for glass size particle >1000 µm and 152.0 µg Hg/g for glass size particle <100 µm); the crushing time required for the optimal removal of mercury from spent tubes is 24 h; on average 71% of the mercury is desorbed at a temperature of 400 °C. The effects of air flow rate, rotation speed and number of balls could not be determined due to wide variations in the results. It is recommended that recycling companies employ processes combining as heating and mixing techniques for the recovery of mercury from lamps in order to both (i) remove as much of the mercury as possible in vapor form and (ii) avoid adsorption of the mercury at new sites created during the crushing process.

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ABSTRACT Conversion of sewage sludge to activated carbon is attractive as an alternative method to ocean dumping for the disposal of sewage sludge. Injection of activated carbon upstream of particulate matter control devices has been suggested as a method to remove elemental mercury from flue gas. Activated carbon was prepared using various activation temperatures and times and was tested for their mercury adsorption efficiency using lab-scale systems. To understand the effect of the physical property of the activated carbon, its mercury adsorption efficiency was investigated as a function of its Brunauer–Emmett–Teller (BET) surface area. Two simulated flue gas conditions, (1) without hydrogen chloride (HCl) and (2) with 20 ppm HCl, were used to investigate the effect of flue gas composition on the mercury adsorption capacity of activated carbon. Despite very low BET surface area of the prepared sewage sludge activated carbons, their mercury adsorption efficiencies were comparable under both simulated flue gas conditions to those of pinewood and coal activated carbons. After injecting HCl into the simulated flue gas, all sewage sludge activated carbons demonstrated high adsorption efficiencies, that is, more than 87%, regardless of their BET surface area. Implications: We tested activated carbons prepared from dried sewage sludge to investigate the effect of their physical properties on their mercury adsorption efficiency. Using two simulated flue gas conditions, we conducted mercury speciation for the outlet gas. We found that the sewage sludge activated carbon had mercury adsorption efficiency comparable to pinewood and coal activated carbons, and the presence of HCl minimized the effect of physical property of the activated carbon on its mercury adsorption efficiency.

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Landfills are considered important sources of mercury for surrounding ecosystems. Methylmercury (MeHg) levels in waste layers have been studied extensively; however, the levels of MeHg in cover soils remain undefined. Here, total mercury (THg) and MeHg concentrations in surface cover soils and soil cores from two landfills in China and possible factors affecting Hg methylation were studied. The mean MeHg concentration in surface cover soils from both landfills was 0.048 ng g-1, suggesting that cover soil layers are not active sites of MeHg production. Soil MeHg concentrations in both landfills were affected little by closure time. In the Jiangcungou landfill, no correlations between MeHg concentration and the measured environmental factors (e.g., THg, soil pH, organic matter (OM), and S) were observed that indicated that these parameters might have indirect effects on MeHg concentration. However, in the Laogang landfill, significant correlations were found between MeHg concentration and the measured environmental factors. The results showed that MeHg concentration in the surface cover soil from area D of the Laogang landfill is regulated mainly by soil pH, OM, and S, and that its vertical distribution in areas C and D is regulated mainly by soil pH and soil OM, respectively. These findings fill a knowledge gap regarding MeHg levels in cover soils and they advance our understanding of Hg cycling in landfills, presenting positive implications for landfill management and risk assessment of MeHg.