Total Hg Concentrations Research Articles

The First Exposure Assessment of Mercury Levels in Hair among Pregnant Women and Its Effects on Birth Weight and Length in Semarang, Central Java, Indonesia.

(1) Background: Methylmercury (MeHg) exposure during pregnancy is an important issue due to its possible adverse health effects on fetus. To contribute the development of assessment system of Hg exposure through fish consumption and health effects on children, we examined the hair Hg levels in pregnant women and birth weight and length. (2) Methods: In 2018, a cohort study was conducted on 118 pregnant women-infant pairs from six community health centers in the northern coastal area in Central Java Indonesia. Data on mothers’ characteristics during pregnancy, birth outcomes, and fish consumption were collected. Total Hg concentrations were determined from hair samples. (3) Results: The median (min-max) of the maternal hair Hg level was 0.434 (0.146–8.105) µg/g. Pregnant women living in lowland areas, near the sea, showed higher hair Hg concentration and fish consumption than those in highland areas {[0.465 (0.146–8.105) vs. 0.385 (0.150–1.956) µg/g; p = 0.043] and [(85.71 (0–500.0) vs. 49.76 (0.0–428.57) g/day; p < 0.01], respectively}. The maternal hair Hg level had no association with baby’s birth weight and length. (4) Conclusions: The median maternal hair Hg is at a low level and had no association with infant birth weight and length in this study subjects.

Differences in Mercury Concentrations in Water and Hydrobionts of the Crimean Saline Lakes: Does Only Salinity Matter?

Of significant scientific and public concern is the high toxicity, significant bioaccumulation, and magnified concentration within the food web of mercury (Hg). Hg content both dissolved and in suspended forms in water as well as in biomass of different hydrobiont taxa was studied in 18 saline lakes in Crimea from 2012 to 2021. The impact of different factors (salinity, seasonality, anthropogenic activities, geological background, etc.) was analyzed. The generalization of data for all lakes showed that the average concentration of Hg in dissolved form was 129 ng L−1, varying over a wide range. The content of Hg in total suspended substrates was an average of 151 ng L−1, and the total content of Hg in lake water averaged 291 ng L−1. Geological background and anthropogenic activities can determine the total Hg content in lakes. In most lakes, a significant positive correlation was noted between the concentration of one, two, or all three indicators of Hg content and the month of the year, with indicators increasing from winter through to autumn. When analyzing the entire data array, a significant positive correlation was found between the concentration of the suspended form of Hg and salinity; such correlation between the concentration of the dissolved form of Hg and salinity was absent. The highest average Hg concentrations in biomasses were noted in Artemia and were the lowest in plants. Geological background and human activity contribute to high Hg content in lakes. Hydrobionts can significantly influence the distribution and behavior of Hg, being an important factor of its cycle in the lakes.

Risk assessment of mercury through dietary exposure in China

Mercury (Hg) is a widespread heavy metal causing various damages to health, while insufficient studies assessed its exposure risk across China. This study explored concentrations in food items and dietary exposure risks across China by comprehensively analyzing the researches on total Hg (THg) in eight food items and methylmercury (MeHg) in aquatic foods published between 1980 and 2021. According to the included 695 studies, the average THg concentration in all food items was 0.033 mg/kg (ranging from 0.004 to 0.185 mg/kg), with the highest concentration in edible fungi. The average daily dietary THg exposure from all foods was 12.9 μg/day. Plant-based foods accounted for 62.7% of the dietary THg exposure. Cereals and vegetables were the primary source of THg exposure. The MeHg concentration in aquatic foods was 0.08 mg/kg, and the average dietary exposure was 3.8 μg/day. Monte Carlo simulations of the dietary exposure risk assessment of THg and MeHg showed that approximately 6.4 and 7.0% of residents exceeded the health-based guidance value set by the European Food Safety Authority, with higher exposure risk in Southwest and South China. The nationwide target hazard quotient index of THg was greater than 1, suggesting that the non-carcinogenic risk of dietary exposure to THg needed further concern. In summary, this study has a comprehensive understanding of dietary Hg exposure risks across China, which provide a data basis for Hg exposure risk assessment and policy formulation.

Distribution of Mercury and Methylmercury in Farmland Soils Affected by Manganese Mining and Smelting Activities.

Manganese (Mn)-related activities would affect the mercury (Hg) cycling in farmlands, whereas this was not well understood. Here, one of the largest Mn ores in China was selected to study the effects of Mn-related activities on the accumulation and distribution of total Hg (THg) and methylmercury (MeHg) in farmland soils. The soil THg concentrations in the mining area were 0.56 ± 0.45, 0.56 ± 0.45, 0.53 ± 0.44, and 0.50 ± 0.46 mg kg−1 in the 0–10, 10–20, 20–30, and 30–40 cm layers, respectively, while they were increased to 0.75 ± 0.75, 0.72 ± 0.60, 0.62 ± 0.46, and 0.52 ± 0.38 mg kg−1 in the smelting area. Similarly, the soil MeHg concentrations in the smelting area were also elevated by 1.04–1.34 times as compared to those in the mining area. Concentrations of THg (0.59 ± 0.50 mg kg−1) and MeHg (0.64 ± 0.82 μg kg−1) in soils were higher than the regional background value but lower than in vicinal Hg-mining areas, while they were largely elevated at the intersection of two rivers in the smelting area. Significant positive Mn-THg relationship (p < 0.01) and negative Mn-MeHg relationship (p < 0.01) favored the conclusion that soil Mn could promote Hg accumulation while inhibiting MeHg production. Approximately 70% of soil Hg was distributed in the residual phase, and the environmental hazard was not elevated according to a geochemical model. Overall, mining and smelting activities of Mn ores have resulted in obvious and distinct effects on the accumulation and methylation of Hg in farmland soils, but the environmental hazards are currently manageable.

Occurrence of mercury in polychaete species (Annelida) and their associated sediments from an important Southern Atlantic Ocean Bay

In the present study, the Hg levels in freshly collected polychaete species and their associated sediments were evaluated from Todos os Santos Bay, Northeastern Brazil. Additionally, it was also measured the Hg distribution along the annelids' body parts (anterior region, abdomen, and posterior region). Total Hg concentration was as follows: 13.6–144 μg kg−1 (Scolelepis chilensis, deposit feeder), 8.2–122 μg kg−1 (Laeonereis acuta, deposit feeder), 95–612 μg kg−1 (Armandia agilis, deposit feeder); 96.6–206 μg kg−1 (Lumbrineris sp., carnivorous), 75.3–112 μg kg−1 (Goniada echinulate, carnivorous), and 115–198 μg kg−1 (Branchiomma sp., suspension feeder). In turn, Hg levels in sediments ranged from 2.77 ± 0.24 to 6.38 ± 0.15 μg kg−1. Hg concentrations found in polychaete soft tissues were higher than those found in the sediments. Specific habits, feeding behavior, trophic level, and stressful environmental conditions are the main factors affecting the Hg levels in the species studied. The bioaccumulation factor (BAF), contamination factor (CF), and ecological risk assessment (Er) were calculated. The BAF values were higher than 1 for all studied species, indicating Hg bioaccumulation in the annelids, but the low levels of CF e Er showed those Hg levels present low to no significant ecological risk for the biota and benthonic organisms living in the sediments. Finally, no statistically significant difference was observed for Hg concentration levels along the polychaete body parts.

Global health impact of atmospheric mercury emissions from artisanal and small-scale gold mining

SummaryArtisanal and small-scale gold mining (ASGM) is the leading source of mercury (Hg), a global neurotoxin. Past research has focused on the health impacts on miners and nearby residents; here, we estimate the risk for global general populations by employing a comprehensive atmosphere-land-ocean-ecosystem and exposure-risk-valuation model framework. Our results suggest that ASGM sources contribute 12%, 10%, and 0.63% to the atmospheric Hg deposition, plankton methylmercury concentrations, and soil total Hg concentrations at present day, respectively, and cause 5.8×105 points of intelligence quotient decrements and 1,430 deaths for global general populations per year. The monetized global health impact of ASGM ($154 billion) is 1.5 times its local impact and accounts for half of the total revenue of ASGM ($319 billion). A major spatial decoupling between the health impact and economic gains is also revealed, suggesting that intervention measures such as awareness-raising, capacity-building, and technology transfer funded by the Global North are cost-effective.

Comparative assessment of blood mercury in American alligators (Alligator mississippiensis) from Coastal North Carolina and Florida.

Mercury (Hg) is a widespread and harmful persistent pollutant of aquatic ecosystems. Except for the northern most populations of American alligators (Alligator Mississippiensis) found in North Carolina, the potential adverse health impacts of Hg on ecosystems and humans consuming alligator meat have been studied for over three decades. Now that alligators are being recreationally hunted and consumed across their range, it is especially important to monitor toxic contaminant levels to best understand possible adverse impacts of exposures on alligator populations and human health. In this study, we determined blood Hg concentrations in American alligators from an urbanized site in Wilmington, NC, a nearby site at Lake Waccamaw, NC, and a site on the St Johns River in Florida. Median blood total Hg (tHg) concentrations were particularly high at Lake Waccamaw (526 ng/g, range 152-946 ng/g), resulting in median muscle concentrations (0.48 mg/kg, range 0.13-0.88 mg/kg) well above US EPA screening values for fish consumption. Median concentrations at the Wilmington site (69 ng/g, range 22-336 ng/g) were generally low, and Hg concentrations from the St Johns River site (143 ng/g, range 54-244 ng/g) were comparable to those reported in previous studies. Analysis of relationships between tHg concentrations and a panel of blood chemistry biomarkers found only modest concentration-dependent impact on biomarkers of renal function. The results of this study reveal that local environmental factors greatly impact Hg bioaccumulation in alligators, findings that reaffirm local contaminant biomonitoring in alligator populations will be critical for affective management and determination of guidelines for safe consumption of harvested alligators.

Element concentrations of cultured fish in the Black Sea: selenium-mercury balance and the risk assessments for consumer health.

Fish are a powerful model for risk-benefit analyses to explore the impact of elements on human health among all accessible species. The sea bream (Sparus aurata), sea bass (Dicentrarchus labrax), turbot (Scophthalmus maximus), and weights of > 1kg large rainbow trout registered as "Turkish Salmon," (Oncorhynchus mykiss) are four economically important cultured species in the Black Sea In this research, it is aimed (1) to determine the value of the elements, (2) to determine total Hg and Se concentrations, Se/Hg molar ratios, and the HBVSe index, and (3) to calculate the consumer's possible health risk in the edible tissues of cultivated four economically important Black Sea fish species. Fish and diet samples from all species were obtained in 2020 from aquaculture locations in the Black Sea (Sinop, Samsun, and Trabzon cites of Turkey). At the end of the study, the elements in all edible tissues and all the parameters analyzed [Se/Hg, estimated daily intake (EDI), target hazard quotient (THQ), maximum allowable consumption rate (CRlim and CRmm)] in cultured fish tissues were below permissible values. Additionally, when compared with the data of the World Health Organization and The National Academy of Sciences, it determined that consuming cultured fish in the Black Sea adequately meets the daily elemental requirement.

Effect of body size, feeding ecology and maternal transfer on mercury accumulation of vulnerable silky shark Carcharhinus falciformis in the eastern tropical pacific

The silky shark Carcharhinus falciformis is a large pelagic species distributed in the global oceans and was recently listed as “Vulnerable” by the IUCN because of its decline in population due to overfishing. As an apex predator, the silky shark can accumulate elevated quantities of mercury (Hg), posing a potential risk to its remaining population. In this study, total Hg (THg) concentrations were determined in silky shark muscle, liver, dermis, red blood cells (RBC) and plasma sampled from the eastern tropical Pacific, and δ15N values were measured to explore the influence of feeding ecology on Hg accumulation. The highest THg concentrations were in muscle (7.81 ± 6.70 μg g−1 dry weight (dw) or 2.14 ± 1.83 μg g−1 wet weight (ww)) and liver (7.88 ± 10.22 μg g−1 dw or 4.66 ± 6.04 μg g−1 ww) rather than dermis, RBC and plasma. The THg concentrations in all tissue types were significantly correlated with fork length and showed faster accumulation rates after maturity. Maternal THg transfer was observed in silky sharks with embryos having 33.16% and 1.98% in muscle and liver compared with their respective mothers. The potentially harmful THg concentrations in silky shark tissues and embryos may lead to health problems of sharks and consumers. THg concentrations were negatively correlated with δ15N values for all tissues, indicating likely baseline variations in δ15N values that reflect changes in the foraging habitats or regions of silky sharks with size or age. Lastly, strong correlations were observed among THg concentrations of all tissue types, indicating that nonlethal sampling of muscle and dermis tissue can be used effectively to quantify THg concentration of other internal tissues.

Hg in the hydrothermal fluids and gases in Baia di Levante, Vulcano, Italy

The importance of fluid and gaseous mercury (Hg) emissions from hydrothermal systems in the shallow, coastal ocean is poorly constrained. However, there are indicators that they could be a significant natural Hg source. We evaluated the hydrothermal Hg emissions around Vulcano Island, Aeolian Arc, Italy, which is host to a marine shallow-water hydrothermal system (MSWHS) in Baia di Levante. Fluids were collected with porewater probes, and gases were collected into Tedlar© bags. Total Hg (THg) concentrations in the hydrothermal fluids ranged from 2.9 to 2888 pM. The concentrations of volatile Hg were below 8 pM and trended positively with increasing temperature. Monomethyl Hg (MMHg) was not detected. Total Hg in the gases ranged from 0.03 to 1.82 μmol/m3.High concentrations of THg were associated with low Cl-concentrations, low pH-values, and high K/Cl and Mg/Cl ratios. Concentrations of THg in the hydrothermal fluids resulted from mixing between meteoric water, seawater, condensed fumarolic vapor, and a deep hydrothermal fluid. However, not all low-Cl fluids were high THg samples. Samples taken along the coast of the La Fossa crater contained substantially less THg (2.9 to 29.4 pM), despite similar hydrothermal indicators as those in the Baia di Levante samples. These data support subsurface circulation models, which discuss the downslope flow of condensed La Fossa crater gases to the coast. In the hydrothermally active area of Baia di Levante, concentrations of THg were elevated relative to background surface seawater, ranging from 40 to 5110 pM. In comparison, the remainder of the bay ranged from 0.8 to 2.4 pM.The flux of Hg to the atmosphere from surface waters was calculated through dissolved Hg concentrations. The flux at each sampled site ranged from 0 to 19.6 pmol/m2/hr. The highest flux rates were determined for those areas with visible hydrothermal activity, particularly those with high gaseous emission rates. Surface water concentrations declined rapidly away from point sources, indicating atmospheric emission, dilution through mixing, or scavenging and sedimentation. In hydrothermally active areas, Baia di Levante sediments contained THg concentrations of 2.42 nmol/g and 49.52 nmol/g, which were significantly above background (0.03 nmol/g).The largest gaseous point source, Bambino, released >2 L of gas per second. Although, Hg concentrations in the gas were low (113 to 122 nmol/m3) relative to other measured point sources near the beach (1768 to 1817 nmol/m3), due to the volume of discharge, surface water concentrations were elevated (131 pM).The Hg present in the hydrothermal system of Vulcano contributes Hg to the atmosphere and local seawater as a natural source.

Mercury Accumulation in a Stream Ecosystem: Linking Labile Mercury in Sediment Porewaters to Bioaccumulative Mercury in Trophic Webs

Mercury (Hg) deposition and accumulation in the abiotic and biotic environments of a stream ecosystem were studied. This study aimed to link labile Hg in porewater to bioaccumulative Hg in biota. Sediment cores, porewaters, and biota were sampled from four sites along the Fourmile Branch (SC, USA) and measured for total Hg (THg) and methyl-Hg (MHg) concentrations. Water quality parameters were also measured at the sediment–water interface (SWI) to model the Hg speciation. In general, Hg concentrations in porewaters and bulk sediment were relatively high, and most of the sediment Hg was in the solid phase as non-labile species. Surface sediment presented higher Hg concentrations than the medium and bottom layers. Mercury methylation and MHg production in the sediment was primarily influenced by sulfate levels, since positive correlations were observed between sulfate and Hg in the porewaters. The majority of Hg species at the SWI were in non-labile form, and the dominant labile Hg species was complexed with dissolved organic carbon. MHg concentrations in the aquatic food web biomagnified with trophic levels (biofilm, invertebrates, and fish), increasing by 3.31 times per trophic level. Based on the derived data, a modified MHg magnification model was established to estimate the Hg bioaccumulation at any trophic level using Hg concentrations in the abiotic environment (i.e., porewater).

A Simplified Drying Procedure for Analysing Hg Concentrations

Mercury (Hg) in peatlands remains a problem of global interest. To mitigate the risks of this neurotoxin, accurate assessments of Hg in peat are needed. Treatment of peat that will be analysed for Hg is, however, not straightforward due to the volatile nature of Hg. The drying process is of particular concern since Hg evasion increases with the temperature. Samples are, therefore, often freeze-dried to limit Hg loss during the drying processes. A problem with freeze-drying is that cost and equipment resources can limit the number of samples analysed in large projects. To avoid this bottleneck, we tested if drying in a 60 °C-degree oven could be an acceptable alternative to freeze-drying. We both freeze-dried and oven-dried (60 °C) 203 replicate pairs of peat samples, and then examined the differences in total Hg concentration. The Hg concentration differed significantly between the two drying methods with a median Hg deficit in oven-dried samples of 4.2%. Whether a 4.2% deficit of Hg depends on one’s purpose. The lower median Hg concentration in oven-dried samples has to be weighed against the upside efficiently drying large sets of peat samples. By freeze-drying a subset of the samples, we fitted a function to correct for Hg loss during oven-drying (y=0.96x+0.08). By applying this correction, the freeze-drying bottleneck could oven-dry large-scale inventories of total Hg in peatlands with results equivalent to freeze-drying, but only have to freeze-dry a subset.

Presence of nano-sized mercury-containing particles in seafoods, and an estimate of dietary exposure

The toxicity of nano-sized particles of mercury (NP–Hg), which are thought to be generated during the detoxification of methyl mercury (MeHg), may differ from that of MeHg, elemental Hg (Hg0), and inorganic Hg (I–Hg). From a human health perspective, it is important to evaluate the presence of NP-Hg in seafoods. We investigated the in vivo formation of NP-Hg in fish and shellfish, which are the main sources of Hg exposure in humans. NP-Hg was measured in 90 fish samples with single-particle inductively coupled plasma mass spectrometry (spICP-MS) after enzyme degradation with pancreatin and lipase. In addition to NP-Hg, total Hg (T-Hg), MeHg, and selenium (Se) concentrations were evaluated. Transient Hg signals were detected as nanoparticles from almost all samples by using spICP-MS. Higher particle number concentrations (CPN) were observed in the tuna–swordfish group than in the shellfish group (17.7 × 107 vs. 1.2 × 106 particles/g, respectively). Although the CPN and maximum particle mass increased significantly with increasing T-Hg concentration, the increase in CPN was greater than those in maximum particle mass. Assuming that the NP-Hg detected was HgSe (tiemannite) and spherical based on previous reports, the maximum particle diameter was estimated to be 89 nm. The mean dietary exposures to NP-Hg, T-Hg, and MeHg were estimated to be 0.067, 5.75, and 5.32 μg/person per day, respectively. Generation of NP-Hg was inferred to be widespread in marine animals, with a preferential increase in the number of particles rather than an increase in particle size. The mean dietary exposure to NP-Hg in Japanese people was estimated to be 1.2 ng/kg body weight (BW) per day. Compared to PTWI of 4 μg/kg BW per week (0.57 μg/kg BW per day) derived by JECFA (2011), the health risk from redissolved I–Hg from NP-Hg is small.

Effect of Biochar on Metal Distribution and Microbiome Dynamic of a Phytostabilized Metalloid-Contaminated Soil Following Freeze-Thaw Cycles.

In the present paper the effectiveness of biochar-aided phytostabilization of metal/metalloid-contaminated soil under freezing–thawing conditions and using the metal tolerating test plant Lolium perenne L. is comprehensively studied. The vegetative experiment consisted of plants cultivated for over 52 days with no exposure to freezing–thawing in a glass greenhouse, followed by 64 days under freezing–thawing in a temperature-controlled apparatus and was carried out in initial soil derived from a post-industrial urban area, characterized by the higher total content of Zn, Pb, Cu, Cr, As and Hg than the limit values included in the classification provided by the Regulation of the Polish Ministry of Environment. According to the substance priority list published by the Toxic Substances and Disease Registry Agency, As, Pb, and Hg are also indicated as being among the top three most hazardous substances. The initial soil was modified by biochar obtained from willow chips. The freeze–thaw effect on the total content of metals/metalloids (metal(-loid)s) in plant materials (roots and above-ground parts) and in phytostabilized soils (non- and biochar-amended) as well as on metal(-loid) concentration distribution/redistribution between four BCR (community bureau of reference) fractions extracted from phytostabilized soils was determined. Based on metal(-loid)s redistribution in phytostabilized soils, their stability was evaluated using the reduced partition index (Ir). Special attention was paid to investigating soil microbial composition. In both cases, before and after freezing–thawing, biochar increased plant biomass, soil pH value, and metal(-loid)s accumulation in roots, and decreased metal(-loid)s accumulation in stems and total content in the soil, respectively, as compared to the corresponding non-amended series (before and after freezing–thawing, respectively). In particular, in the phytostabilized biochar-amended series after freezing–thawing, the recorded total content of Zn, Cu, Pb, and As in roots substantially increased as well as the Hg, Cu, Cr, and Zn in the soil was significantly reduced as compared to the corresponding non-amended series after freezing–thawing. Moreover, exposure to freezing–thawing itself caused redistribution of examined metal(-loid)s from mobile and/or potentially mobile into the most stable fraction, but this transformation was favored by biochar presence, especially for Cu, Pb, Cr, and Hg. While freezing–thawing greatly affected soil microbiome composition, biochar reduced the freeze–thaw adverse effect on bacterial diversity and helped preserve bacterial groups important for efficient soil nutrient conversion. In biochar-amended soil exposed to freezing–thawing, psychrotolerant and trace element-resistant genera such as Rhodococcus sp. or Williamsia sp. were most abundant.

Mercury (Hg) geochemistry of mid-ocean ridge sediments on the Central Indian Ridge: Chemical forms and isotopic composition

To geochemically characterize mercury (Hg) in the deep-sea ridge environment, the total concentration, chemical forms (sequential leaching extraction), and isotopic compositions of Hg in surface sediments from the middle portion of the Central Indian Ridge were investigated. Highly elevated Hg concentrations (up to 13,000 ng/g) in sediments near the hydrothermal vent are associated with intense hydrothermal activity driven by serpentinization. The hydrothermal impact on these sediments is also evident in the REECN fractionation pattern with a remarkably strong positive europium (Eu) anomaly. Most volcanic and hydrothermal Hg in the study area is preferentially precipitated with sulfides; in the hydrothermal vent area, however, scavenging by Fe-Mn hydroxides is another significant removal pathway of Hg. Thus, such precipitation and production of sulfides and hydroxides are a major cause of local enrichment of Hg around the mid-ocean ridge. Most sediments show limited or no mass-independent fractionation (Δ199Hg = +0.02 ± 0.21‰, 2σ, n = 15), indicating that syngenetic magmatic or mantle-derived materials are the dominant Hg source. However, the large variation in mass-dependent fractionation was observed, especially in the vent-distal sediments (δ202Hg = −1.10 ± 0.80‰, 2σ, n = 11), which occurred mainly during the formation of the sulfides and may be associated with preferential precipitation of lighter isotopes. Our study demonstrates that an off-axis high-temperature hydrothermal system driven by exothermic serpentinization of ultramafic mantle rocks may serve as a significant Hg source and provides further insights into grasping the behavior of hydrothermal and volcanogenic Hg in active deep-sea ridge systems.

Concentrations and Species of Mercury in Municipal Sludge of Selected Chinese Cities and Potential Mercury Emissions From Sludge Treatment and Disposal

Municipal sewage has been identified as an important source of mercury (Hg) to the environment, and sewage sludge is the major sink of sewage-borne Hg. Knowledge of Hg species in sludge and potential Hg emissions during sludge treatment/disposal is still limited. A survey on Hg concentrations and species in sewage sludge of 16 provinces and municipalities in China was conducted. Hg was detected in all sewage sludge samples, with total Hg (THg) concentrations ranging from 0.3 to 7.7 mg/kg. Results from sequential chemical extractions (SCE) indicated that sludge-borne Hg mainly occurred in the form of Hg sulfide, with a small amount of organo-chelated Hg (Hg-OM) and HgO, and a negligible amount of soluble Hg. Thermal decomposition results indicated that Hg is generally released from sludge at a temperature range of 200–400°C, with the highest release at 250–350°C (38%–86%), consistent with the thermal decomposition of HgS, Hg-OM, and HgO. THg in sewage samples under ventilation at room temperature remained constant over a month period, indicating negligible Hg emission under such conditions. The mass loading of sludge-borne THg in China for year 2019 was estimated to be 30 tons, about 3.6% of the total anthropogenic THg released (including direct and secondary anthropogenic releases) in China. At the temperature range for sludge incineration, sludge carbonization, and sludge/brick/cement production, most of the Hg in sludge will be released to air due to thermal decomposition of Hg compounds. As such, Hg-capture systems are essential in sludge treatment processes involving high temperatures.

Mercury in the brain (tumor tissues) and in markers (hair and blood) of exposure in Western Amazonia patients

BackgroundCentral nervous system tumors (CNSTs) represent the second most frequent form of malignant tumors in childhood and the second leading cause of death associated with neurological diseases, affecting individuals of all age groups. In adults, CNSTs are the sixth most common cause of death in patients with malignant tumors. Additionally, the brain is the most sensitive and studied organ for mercury (Hg) toxicity. MethodWe studied total Hg (THg) in tissue samples (of benign and malignant CNSTs) and explored its associations with THg in exposure markers (hair and blood) from 65 patients (40 females and 25 males) who underwent surgical treatment. ResultsNo statistically significant differences were found in THg concentrations in brain tumors or in blood and hair from these patients (classified as malignant/benign or glioma/non-glioma); also, there were no statistically significant differences between males and females. However, statistically significant correlations were found between THg in CNSTs and in hair (rs = 0.4967; p = 0.0001) and in blood (rs = 0.4702; p = 0.0058); but no significant correlations were found between THg in hair and blood (rs = 0.1229; p = 0.5332). In the Western Amazon, with endemic exposure to fish-methylmercury, these urban patients were low to moderate fish consumers; THg concentrations in blood (median: 0.645 µg.L−1; range: 8.01–21.02 µg.L−1; n = 56) and hair (median: 0.686 µg.g-1; range: 0.01–10.02 µg.g−1; n = 65) were relatively low, whereas THg levels in brain tumors (median: 8.194 ng.g−1; range: <0.10–69.16 ng.g−1; n = 65) were within range of published studies in brain autopsies. Additionally, no statistically significant correlations (p = 0.4828) were observed between frequency of fish consumption and THg in the brain. ConclusionAlthough no significant THg concentrations in the type of brain tumors (benign versus malignant) were found, the significantly positive correlation between markers of THg exposure (hair and blood) and THg in the brain tissues indicates its usefulness as a marker/proxy for brain-THg load. These findings confirm the value of using hair and blood as constructs of THg in the brain of exposed populations.

Tracing concealed gold deposits using mercury isotopes in surface soils: A study from the Shuiyindong gold deposit, Guizhou province, China

Surface soil sampling has been proved to be an effective and low-cost mineral exploration method in covered terrains. The critical question is to determine whether the surface anomalies originated from the mineralization at depth. Mercury isotope signatures have recently been employed as a tool for understanding the sources of Hg anomalies. Meanwhile, Hg is a traditional pathfinder for Au exploration. Can Hg isotopes be applied to trace the sources of Au anomalies in topsoils in covered areas? This is the first study that employed Hg isotopes as an exploration proxy for Au mineralization at depth. Surface soil samples over the concealed Shuiyindong Au deposit, China, were collected and their total Au (TAu), total Hg (THg) contents, and Hg isotope compositions were analyzed. Gold and Hg surface positive anomalies display high correlation indexes along the sampled traverse above the Shuiyindong Au deposit. Moreover, the Hg anomaly is significantly stronger than that of Au. Soils from deep ores-related areas show clearly positive δ202Hg values (−0.78‰ to −0.23‰, averaging −0.46 ± 0.19‰, n = 10, 1SD) compared with those from the background areas (−1.67‰ to −0.66‰, averaging −1.07 ± 0.28‰, n = 10, 1SD). δ202Hg and 1/THg in deep ores-related soils have been altered by the ascending geogas from the mineralized rocks of the Longtan Fm. Soil positive Au anomalies detected in the study area are sourced at depth in the Shuiyindong Au deposit. However, it is not feasible to apply Δ199Hg to trace the anomalous Au sources in topsoils, because Hg(II) photoreduction can imprint the Δ199Hg signature, leading to negative Δ199Hg values in the soils. Semi-volatile Hg and ultra-fine Au particles are mobile and could continuously migrate from the depth to the surface through macro-structures and micro-fractures with the ascending geogas, then most of them are absorbed by the surface soils. Overall, this study successfully traced the Au deposit at >650 m depth using δ202Hg, which is significant for mineral exploration of deep-seated Au deposits, especially in unknown covered areas.

Using dissolved organic matter fluorescence to predict total mercury and methylmercury in forested headwater streams, Sleepers River, VermontUSA

AbstractAqueous transport of mercury (Hg) across the landscape is closely linked to dissolved organic matter (DOM). Both quantity and quality of DOM affect Hg mobility, as well as the formation and transport of toxic methylmercury (MeHg), but only a limited number of field studies have investigated Hg and MeHg with respect to specific DOM components. We investigated these interactions at the 41‐ha forested W‐9 catchment at Sleepers River, Vermont, which has a long history of mercury and other biogeochemical research. We examined spatial and temporal patterns of filtered Hg fractions and dissolved organic carbon (DOC) concentration, DOM quality, and major solutes at 12 stream sites within W‐9 and the downstream W‐3 gage (837 ha) over five sampling campaigns including a large (79 mm) fall storm, spring snowmelt, and three seasonally contrasting base flow periods. Filtered total Hg (THg), MeHg, and DOC concentrations increased in order base flow &lt; snowmelt &lt; fall storm, except that MeHg remained at baseflow levels during snowmelt. Ranges of median concentrations across sites for the five campaigns were THg, &lt;0.2–4.1 ng L−1; MeHg, &lt;0.03–0.45 ng L−1; and DOC, 0.8–14.0 mg L−1. Humic‐like DOM fluorescence components, as determined by parallel factor analysis (PARAFAC), dominated the fluorescence across sites and sampling campaigns. THg correlated strongly (r &gt; 0.94) with these humic components, but even more strongly with bulk DOC and absorbance at 254 nm (UV254;r &gt; 0.96), and less strongly with protein‐like DOM (0.7 &lt; r &lt; 0.9). MeHg correlated in the same order but less strongly with humic‐ (0.8 &lt; r &lt; 0.9) and protein‐like (0.6 &lt; r &lt; 0.8) DOM. MeHg increased in summer, potentially in response to enhanced microbial production in warmer periods. MeHg formation may have been linked to protein‐like DOM, but its transport was linked to humic‐like DOM.

Accumulation of the Toxic Metal Mercury in Multiple Tissues of Marine-Associated Birds from South Florida.

One of the best studied global "hot spots" for ecological mercury (Hg) contamination is south Florida (USA), where elevated Hg concentrations in environmental media and regional wildlife were first described over thirty years ago. While Hg contamination has lessened in this region, it is still critical to monitor Hg uptake and potential risks in south Florida wildlife, especially in marine-associated birds, which are known to accumulate potentially toxic Hg levels. In this study, total Hg (THg) concentrations were measured in liver, kidney, muscle, and feathers of 101 individuals from seven species of south Florida birds: brown pelican Pelecanus occidentalis, double-crested cormorant Phalacrocorax auratus, herring gull Larus argentatus, laughing gull Leucophaeus atricilla, northern gannet Morus bassanus, royal tern Thalasseus maximus, and osprey Pandion halietus. A sizeable proportion of individuals (> 40%) were found to contain THg concentrations in internal tissues that exceeded estimated toxicity thresholds for Hg-related effects. Certain species, especially osprey, were found to exhibit a higher rate of threshold exceedances than others and should continue to be monitored for Hg-related effects in future studies. Feather THg concentrations exhibited a lower rate of toxicity threshold exceedances (12%) and were not significantly correlated with those in internal tissues in most cases, suggesting that they may not be well suited for monitoring Hg exposure in these species unless sources of data variation can be better understood. The results of the present study contribute significantly to our understanding of trends in Hg accumulation and Hg-related health risks in south Florida marine-associated birds.