Hg Concentrations In Water Research Articles

Sources, Fates, and Geochemical Cycling of Mercury in Geothermal Fields: Insights From Mercury Isotopes

AbstractGeothermal fields emit remarkable amounts of mercury (Hg) to the environment. To address the source, fate and geochemical cycling of Hg in geothermal fields, we investigated Hg concentrations and isotopic compositions of hot spring water and fumarole gases from Rehai and Dagejia in SW‐China. Elevated Hg concentrations in fumarole gases (10.0–167 ng m−3) and hot spring water (3.44–84.5 ng L−1) were observed, suggesting that both geothermal fields are of environmental concern. The variation in Δ199Hg (−0.06 to 0.23‰) and Δ200Hg (−0.09 to 0.19‰) in hot spring water supports Hg likely originating from endogenous volcanic degassing and/or rainwater. Negative and nearly zero Δ199Hg in fumarole gases (−0.32 to 0.03‰) supports volcanic degassing and background atmosphere origin. The ranges of δ202Hg in fumarole gases (−0.74 to 0.59‰) and hot spring water (−1.29 to 0.52‰) could reflect limited fluids boiling in geothermal fields. This study, thus, fills an important knowledge gap regarding Hg global cycling.

The effect of phytoremediation on the reduction of mercury-contaminated water from gold processing using water kale (Ipomoea aquatica Forsk)

Gold ore processing is carried out by amalgamation techniques where mercury (Hg) is used as a medium to bind gold which results in water pollution around the processing area, so it is necessary to remediate water. One way in managing mercury-contaminated water is phytoremediation of the use of water kale (ipomoea aquatica forsk) and to help the phytoremediation process, ingredients are needed that can help the growth of water kale in increasing the absorption of Hg concentrations, namely the addition of liquid NPK fertilizer. This study aims to analyze water kale without liquid NPK fertilizer, and use liquid NPK fertilizer against water kale in reducing the concentration of Hg, pH and TSS metals in water. This study used an experimental method with an experimental box (container) consisting of 4 treatments, then an Analysis of Variance (ANOVA) test of 5% and Duncan Multiple Rang Test were carried out. The results showed that liquid NPK fertilizer had an influence on reducing the concentration of Hg, pH and TSS in water. Based on the results of experiments using liquid NPK fertilizer, the best treatment results were obtained in mercury absorption by water kale and reducing Hg concentration in water, namely treatment D (contaminated water + water kale + liquid NPK fertilizer) on the 14th day, as evidenced by a decrease in Hg concentration in water by 0.56 mg / l to 0.00486 mg / l, pH 10.1 to 6.86 and TSS 1695 mg / l to 1 mg / l and an increase in nitrate levels, Phosphate and potassium in water can accelerate absorption by water kale.

Bionanomaterial composed of Bradyrhizobium japonicum and graphene oxide for determination of mercury in water and fruit juice samples

In the present work, the synthesis of a novel hybrid bionanomaterial formed by the bacteria Bradyrhizobium japonicum (BJ) and the graphene oxide (GO) nanomaterial implemented in the miniaturized dispersive microsolid phase extraction technique (D-μ-SPE) was reported for the first time for the preconcentration and determination of Hg in water and fruit juice samples after a multivariate optimization. Selective Hg extraction was achieved by forming a complex with ammonium pyrrolidinedithiocarbamate (APDC) reagent and a multivariate study was performed to optimize the experimental conditions. The optimal Hg extraction conditions for 25 mL of sample were 3 mg of BJ@GO, NaNO3 at 1% (w/v), 6 min of vortex agitation and 9 min of centrifugation. For back extraction, 500 µL of 14 mol L−1 HNO3, 6 min of vortex agitation and 6 min of centrifugation were used followed by detection by cold vapor atomic fluorescence spectrophotometry (CV-AFS). Under optimized experimental conditions, an extraction efficiency of 98%, a detection limit of 0.08 µg L−1, a relative standard deviation of 3.5% (at 1 µg L−1 of Hg, n = 10), and a linear range of 0.26 - 4.0 µg L−1 were obtained. In addition, the sustainability of the method developed through the use of the Analytical GREEnness calculator (AGREE) software was evaluated, obtaining a greenness degree of 0.59. This work reports the first application of BJ@GO along with the D-μ-SPE technique for trace Hg determination water and fruit juice samples. In this way, this research work allows the exact and precise determination of low Hg concentrations in water and juice samples, which allows the evaluation of the contamination degree by this toxic metal in beverages widely consumed by the population.

Field method for preservation of total mercury in waters, including those associated with artisanal scale gold mining.

Analysis of mercury (Hg) in natural water samples has routinely been impractical in many environments, for example, artisanal and small-scale gold mines (ASGM), where difficult conditions make monitoring of harmful elements and chemicals used in the processes highly challenging. Current sampling methods require the use of hazardous or expensive materials, and so difficulties in sample collection and transport are elevated. To solve this problem, a solid-phase extraction-based method was developed for the sampling and preservation of dissolved Hg in natural water samples, particularly those found around ASGM sites. Recoveries of 85% ± 10% total Hg were obtained during 4 weeks of storage in refrigerated (4 °C, dark) and unrefrigerated (16 °C, dark) conditions, and from a representative river water spiked to 1 μg L-1 Hg2+, 94% ± 1% Hg recovery was obtained. Solid-phase extraction loading flow rates were tested at 2, 5, and 10 mL min-1 with no breakthrough of Hg, and sorbent stability showed no breakthrough of Hg up to 2 weeks after functionalisation. The method was deployed across five artisanal gold mines in Kakamega gold belt, Kenya, to assess Hg concentrations in mine shaft water, ore washing ponds, and river and stream water, including drinking water sources. In all waters, Hg concentrations were below the WHO guideline limit value of 6 μg L-1, but drinking water sources contained trace concentrations of up to 0.35 μg L-1 total Hg, which may result in negative health effects from long-term exposure. The SPE method developed and deployed here is a robust sampling method that can therefore be applied in future Hg monitoring, toxicology, and environmental work to provide improved data that is representative of total dissolved Hg in water samples.

Geochemical dynamics of phosphorus and metals in sediments of a shallow coastal lake (Xuño Lake, Galicia-NW Iberian Peninsula)

The shallow lakes are important freshwater ecosystems, since they support much of biodiversity and ecosystem services of life on land. Shallow lakes are highly dynamic ecological entities that can exist in several alternative stable states through regime shift caused by a natural or human disturbance that exceeds ecological thresholds for biological communities composition and structure equilibria. The sediment as a reservoir has a key role in the limnological regulation of wetlands linked to the fluxes of nutrients and elements in the biogeochemical interplay with the water and macrophytes. For this reason, the role of sediment in the limnology of the shallow coastal lake of Xuño (NW Iberian Peninsula) was explored by seasonally monitoring the chemical composition of water and sediments, also according to macrophyte species. The shallow depth determines the high availability of light in the bottom and a well-mixed water column maintain the surface of the water–sediment interface oxygenated. The oxic conditions of the bottom implies a top-down regulation of the water column in the Xuño shallow lake that limits the diffusion of phosphorus and trace metals (Fe, Mn, Cu, and Co) to the water, buffering eutrophication or contamination levels by immobilization in the sediments. In fact, the concentration of Hg in the lake water in spring, and also its bioavailability, are high due to its release from the sediment in suboxic conditions. The cover of helophyte species Phragmites Australis and Schoenoplectus Lacustris showed differences in the assimilation of organic monoester and diester phosphorus forms in the sediment. However, the water of the Xuño Lake shows an eutrophic status by the nutrient input associated with the birds populations as indicated by microbiological data.

Human health risk assessment due to mercury use in gold mining areas in the Ecuadorian Andean region

Mining activity drives economic development and has established itself as one of the main industrial spheres globally. However, illegal, and artisanal gold mining, which uses mercury (Hg), is a major source of global pollution. Hg is highly toxic and persistent in the environment, affecting human health and the ecosystem. The objective of this research is to; (a) analyze Hg concentrations in surface waters of nine provinces of the Andean region of Ecuador and compare them with the maximum permissible limits of Ecuadorian regulations, and (b) evaluate the health risk of people exposed to waters with high Hg content through residential and recreational scenarios. In this study, 147 water samples from rivers and streams were analyzed. The results revealed worrying levels of Hg, especially in the provinces of Azuay and Loja where Hg values of up to 0.0913 mg/L and 0.0387 mg/L, respectively, were detected. In addition, it was found that 45% of the samples did not meet the water quality criteria for the preservation of aquatic life, which represents a severe risk to the ecosystem. The probabilistic risk analysis yielded values that exceeded the acceptable exposure limit for adults and children in residential settings in Azuay and Loja, while in the recreational scenario the safe exposure limit was exceeded for both receptors only in the province of Azuay. The elevated presence of Hg in the provinces, mainly in Azuay and Loja, possibly related to illegal gold mining activity, represents a threat to water quality and aquatic life in the Andean region of Ecuador. Children are especially vulnerable, and effective regulation is required to ensure the safety of the population. This study provides valuable information for decision makers regarding the risk associated with Hg exposure in areas of mining activity in the Ecuadorian Andean region. In addition, it can contribute to the development of policies and strategies to control contamination in mining environments and protect human and environmental health in the region.

Coastal streams and sewage outfalls: Hot spots of mercury discharge, pollution and cycling in nearshore environments

The coastal streams (CSs) and sewage outfalls (SOs) are widely distributed and direct anthropogenic stress on global coastal ecosystems. However, the CS/SO-associated mercury (Hg) discharge, pollution and cycle in nearshore environment are less quantified. Here, we report that total Hg (THg) and methylmercury (MMHg) concentrations in waters of CSs (n = 8) and SOs (n = 15) of the northern China were ∼102 to 103 times of coastal surface waters and 10 to 102 times of major rivers in China and other regions. The CS/SO discharges resulted in the increase of total organic carbon (TOC) contents, THg and MMHg concentrations and TOC-normalized THg and MMHg concentrations in sediments of CS/SO-impacted coasts. The laboratory experiments further illustrated that the CS/SO-impacted sediments characterized with high potentials of dissolved THg and MMHg productions and releases. Our findings indicate that the layout optimization of SOs is able to reduce the Hg risk in coastal environment.

Seasonal characterization of mercury contamination along the Portuguese coast: human health and environmental risk assessment

A seasonal characterization of mercury (Hg) accumulation in three different estuaries along the Portuguese coast (i.e. Ria de Aveiro, Tagus estuary and Ria Formosa) was done. For that, it was evaluated: (1) Hg concentrations in abiotic (water) and biotic matrices (flora and fauna); (2) the risk of consumption of local seafood species (e.g. bivalves) to human health; and (3) the environmental risk to Hg exposure. During 1 year, water and biological samples were collected during low tide, in each system for Hg quantification. Our findings revealed that total Hg concentrations in surface waters were higher in Ria de Aveiro and Tagus estuary than in Ria Formosa. In Ria de Aveiro, a particular attention should be given in autumn periods, where Hg levels (≈ 100 µg L−1) were considered quite high according to European quality parameters. The same was observed for the Tagus estuary during spring time. Regarding macrofauna Hg levels, no clear seasonal trend was observed. Also, total Hg concentrations in edible species (< 0.5 µg. g−1 ww) represent no risk for consumption. However, considering the environmental risk, in Ria de Aveiro, there is a moderate risk (RQ > 0.1) in autumn periods, which can be a matter of concern.

Mercury and methylmercury in Hg-contaminated paddy soil and their uptake in rice as regulated by DOM from different agricultural sources.

In this study, from the perspectives of structural and compositional variations of soil-dissolved organic matter (DOM), we explored the effects of agricultural DOM inputs on methylmercury (MeHg) accumulation in the soil and mercury (Hg) bioaccumulation in rice grains. Pot experiments with the addition of DOMs from maize straw (MaS), rape straw (RaS), rice straw (RiS), composted rice straw (CRiS), cow dung (CD), and composted cow dung (CCD) were then conducted. Results showed that, relative to the control, the DOM amendment from each agricultural source elevated MeHg concentrations in the soil, with an increase of 18-227%, but only parts of DOMs elevated total dissolved Hg (DHg) and MeHg (DMeHg) concentrations in pore water. Among all DOM species, RiS, CRiS, and CCD significantly increased total Hg (THg) and MeHg contents in rice grains by 34-64% and 32-118%, respectively. Compared with RiS, THg and MeHg contents in rice grains in the CRiS treatment decreased slightly, which was consistent with the distributions of DHg and DMeHg concentrations in pore water and the aromaticity variation of soil DOM. In contrast, the CCD input significantly enhanced the enrichment of THg and MeHg in rice grains relative to CD because it significantly reduced the humification of soil DOM at all rice-growing stages while increasing the low-molecular-weight fractions in soil DOM. The THg and MeHg contents in the rice grains were significantly lower treated by RaS than those by MaS and RiS, which may be related to the higher sulfur-containing compounds such as sulfate and cysteine in rape straw or its DOM solution. Overall, DOM amendment from different agricultural sources resulted in significantly discriminative effects on the MeHg accumulation in soil and Hg enrichment in rice in the Hg-contaminated paddy field by shaping soil DOM properties.

Understanding drivers of mercury in lake trout (Salvelinus namaycush), a top-predator fish in southwest Alaska's parklands

Mercury (Hg) is a widespread element and persistent pollutant, harmful to fish, wildlife, and humans in its organic, methylated form. The risk of Hg contamination is driven by factors that regulate Hg loading, methylation, bioaccumulation, and biomagnification. In remote locations, with infrequent access and limited data, understanding the relative importance of these factors can pose a challenge. Here, we assessed Hg concentrations in an apex predator fish species, lake trout (Salvelinus namaycush), collected from 14 lakes spanning two National Parks in southwest Alaska, U.S.A. We then examined factors associated with the variation in fish Hg concentrations using a Bayesian hierarchical model. We found that total Hg concentrations in water were consistently low among lakes (0.11–0.50 ng L−1). Conversely, total Hg concentrations in lake trout spanned a thirty-fold range (101–3046 ng g−1 dry weight), with median values at 7 lakes exceeding Alaska's human consumption threshold. Model results showed that fish age and, to a lesser extent, body condition best explained variation in Hg concentration among fish within a lake, with Hg elevated in older, thinner lake trout. Other factors, including plankton methyl Hg content, fish species richness, volcano proximity, and glacier loss, best explained variation in lake trout Hg concentration among lakes. Collectively, these results provide evidence that multiple, hierarchically nested factors control fish Hg levels in these lakes.

Efficient and selective removal of Hg(II) from water using recyclable hierarchical MoS2/Fe3O4 nanocomposites

Developing practical and cost-effective adsorbents with satisfactory mercury (Hg) remediation capability is indispensable for aquatic environment safety and public health. Herein, a recyclable hierarchical MoS2/Fe3O4 nanocomposite (by in-situ growth of MoS2 nanosheets on the surface of Fe3O4 nanospheres) is presented for the selective removal of Hg(II) from aquatic samples. It exhibited high adsorption capacity (∼1923.5 mg g −1), fast kinetics (k2 ∼ 0.56 mg g −1 min−1), broad working pH range (2–11), excellent selectivity (Kd > 1.0 × 107 mL g −1), and great reusability (removal efficiency > 90% after 20 cycles). In particular, removal efficiencies of up to ∼97% for different Hg(II) concentrations (10–1000 μg L −1) in natural water and industrial effluents confirmed the practicability of MoS2/Fe3O4. The possible mechanism for effective Hg(II) removal was discussed by a series of characterization analyses, which was attributed to the alteration of the MoS2 structure and the surface coordination of Hg-S. The accessibility of surface sulfur sites and the diffusion of Hg(II) in the solid-liquid system were enhanced due to the advantage of the expanded interlayer spacing (0.96 nm) and the hierarchical structure. This study suggests that MoS2/Fe3O4 is a promising material for Hg(II) removal in actual scenarios and provides a feasible approach by rationally constructing hierarchical structures to promote the practical applications of MoS2 in sustainable water treatments.

Mercury in Selected Abiotic and Biotic Elements in Two Lakes in Poland: Implications for Environmental Protection and Food Safety

Mercury, which tends to bioaccumulate and biomagnify in aquatic food webs, poses a potential health risk to wildlife and to consumers of predatory fish in particular. Its concentration in biota can be high even at low environmental concentrations. Therefore, the aim of this study was to determine mercury in both abiotic (water and sediment) and biotic elements (common reed (Phragmites australis) and fish: pike (Esox lucius), bream (Abramis brama) and roach (Rutilus rutilus)) in the context of assessing the pollution of two lakes in Poland and the safety of fish consumers. The possibility of Hg biomagnification in fish was also considered. Mercury was determined by means of cold vapor atomic absorption spectrometry (CVAAS). The concentrations of Hg in water and bottom sediments of Lake Ińsko were lower than in Lake Wisola. In the bottom sediments of both lakes, a positive correlation was found between the Hg content and organic matter. The concentration of mercury in the organs of common reed did not exceed 0.017 mg/kg dry weight (dw), and its distribution can be presented as follows: root > leaves > stems > rhizomes. In fish organs from both lakes, the average mercury content did not exceed 0.086 mg/kg of wet weight (ww) and in most cases it was the highest in pike. Higher values were only observed in the muscles and skin of roach. This indicates a lack of biomagnification in the relationships between planktivorous-predatory and benthivores-predatory fish. Based on the maximum levels of mercury in fish and the calculated parameters, i.e., estimated daily intake (EDI), target hazard quotient (THQ) and tolerable weekly intake (TWI), the muscles of the examined fish were found to be safe for consumption. The average dietary exposure to total mercury (THg) and methylmercury (MeHg) was below 0.3% of the TWI.

Mercury migration to surface water from remediated mine waste and impacts of rainfall in a karst area – Evidence from Hg isotopes

Mine waste (MW) in historical mercury (Hg) mining areas continuously emits Hg into local environment, including aquatic ecosystems. Tracing Hg migration process from MW and determining its relative contribution to Hg pollution is critical for understanding the environmental impact of MW remediation. In this study, we combined data of Hg concentration, speciation, and isotope to address this issue in the Wanshan Hg mining area in southwest China. We found that rainfall can elevate Hg concentrations in river water and control the partitioning and transport of Hg in karst fissure zones through changing the hydrological conditions. A consistently large offset of δ202Hg (1.24‰) was observed between dissolved Hg (DHg) and particulate Hg (PHg) in surface water during the low-flow period (LFP), which may have been related to the relatively stable hydrologic conditions and unique geological background (karst fissure zones) of the karst region (KR). Results from the ternary Hg isotopic mixing model showed that, despite an order of magnitude reduction in Hg concentration and flux in river water after remediation, the remediated MW is still a significant source of Hg pollution to local aquatic ecosystems, accounting for 49.3 ± 11.9% and 37.8 ± 11.8% of river DHg in high flow period (HFP) and LFP, respectively. This study provides new insights into Hg migration and transportation in aquatic ecosystem and pollution source apportionment in Hg polluted area, which can be used for making polices for future remediation actions.

Mercury Sources, Emissions, Distribution and Bioavailability along an Estuarine Gradient under Semiarid Conditions in Northeast Brazil

In the semiarid coast of northeast Brazil, climate change and changes in land use in drainage basins affect river hydrodynamics and hydrochemistry, modifying the estuarine environment and its biogeochemistry and increasing the mobilization of mercury (Hg). This is particularly relevant to the largest semiarid-encroached basin of the region, the Jaguaribe River. Major Hg sources to the Jaguaribe estuary are solid waste disposal, sewage and shrimp farming, the latter emitting effluents directly into the estuary. Total annual emission reaches 300 kg. In that estuary, the distribution of Hg in sediment and suspended particulate matter decreases seaward, whereas dissolved Hg concentrations increase sharply seaward, suggesting higher mobilization at the marine-influenced, mangrove-dominated portion of the estuary, mostly in the dry season. Concentrations of Hg in rooted macrophytes respond to Hg concentrations in sediment, being higher in the fluvial endmember of the estuary, whereas in floating aquatic macrophytes, Hg concentrations followed dissolved Hg concentrations in water and were also higher in the dry season. Animals (fish and crustaceans) also showed higher concentrations and bioaccumulation in the marine-influenced portion of the estuary. The variability of Hg concentrations in plants and sediments agrees with continental sources of Hg. However, Hg fractionation in water and contents in the animals respond to higher Hg availability in the marine-dominated end of the estuary. The results suggest that the impact of anthropogenic sources on Hg bioavailability is modulated by regional and global environmental changes and results from a conjunction of biological, ecological and hydrological characteristics. Finally, increasing aridity due to global warming, observed in northeast Brazil, as well as in other semiarid littorals worldwide, in addition to increased water overuse, augment Hg bioavailability and environmental risk and exposure of the local biota and the tradition of human populations exploiting the estuary's biological resources.

Geochemical Characterisation and Health Concerns of Mineral Bottled Waters in Catalonia (North-Eastern Spain)

Spain currently produces around 7000 million litres of mineral water a year, of which about 20% is produced in Catalonia, and there is a need for greater regulation and research into bottled waters and their impact on human health. A total of 29 samples were analysed from different brands of commercially bottled water, and 71 chemical elements were determined in each sample. The aim was to classify each brand based on composition, compare lithological origins, verify compliance with international standards for drinking water, and report benefits for human health. More than 60% of the samples were of the calcium bicarbonate type, had a low mineral content, and were associated with granitic aquifers, ranging from leucogranites to granodiorites. In contrast, 17% were of the sodium bicarbonate type, had harder waters, and were related to thermal springs. The thermal springs of the bottled waters from the Montseny-Guilleres massif (Vichy Catalán, Malavella, and San Narciso) emerge at a temperature of 60 °C with their own natural gas. Two samples exceeded European standards for As and Hg concentrations in water for human consumption, while one showed a concentration of U greater than that set out in international recommendations.

Effects of illegal gold mining on Hg concentrations in water, Pistia stratiotes, suspended particulate matter, and bottom sediments of two impacted rivers (Paraíba do Sul River and Muriaé River), Southeastern, Brazil.

Recent reports of illegal small-scale alluvial gold mining activities (locally called garimpo) by miners working on rafts in the Paraíba do Sul River (PSR) and in one of its tributaries (Muriaé River (MR)) have raised concerns about Hg contamination. This study aimed to evaluate the impact of garimpo activities on Hg contamination in three environmental compartments. Water, sediment, and aquatic macrophytes (Pistia stratiotes) were sampled during the rainy season in PSR, forming a 106-km transect from the point where garimpo rafts were seen and/or seized by the Federal Police. They were also sampled in the MR. Total and dissolved mercury (Hg) concentrations in water and total Hg in the suspended particulate matter (SPM) sampled in the PSR increased by 1.7, 1.5, and 2.1 times at the points where the rafts were seen compared to the point immediately upstream. In the MR, Hg concentrations were higher than those in the PSR, but most values in the environmental compartments were below the safe limits (174–486 ng∙g−1, threshold and probable effect level, respectively), with the exception of Hg in the SPM of one of the MR sampling points (256 ng∙g−1) and the mining tailings (197 ng∙g−1). Sediment granulometry was exponentially associated with Hg concentrations in the sediment (R2 = 0.75, p < 0.0001) and is also essential to understand the physical impacts of garimpo on PSR. Future studies should focus on assessing the seasonal variability of Hg concentrations in the studied compartments, especially if garimpo is identified during the dry season.Supplementary InformationThe online version contains supplementary material available at 10.1007/s10661-022-10477-y.

Mercury, organic matter, iron, and sulfur co-cycling in a ferruginous meromictic lake

Mercury (Hg) speciation in natural waters is controlled by redox conditions and microbiological activity. Water columns of meromictic lakes have large and stable redox chemical and biological gradients that allow the investigation of many Hg chemical transformations. In this study, Hg speciation (elemental Hg = Hg0, methylated Hg = MeHg) and partitioning between truly dissolved (<3 kDa), colloidal (<0.45 μm and >3 kDa), and particulate (>0.45 μm) fractions, were determined throughout a high-resolution water column profile in the ferruginous meromictic Lake Pavin (Massif Central, France) in July 2018. Total Hg concentrations (THg) in water ranged between 0.4 and 8.8 pmol L−1. The particulate phase represented 10–70% of the THg, with a peak found in the mesolimnion associated with the particulate organic carbon maximum. In the mesolimnion, the colloidal fraction represented 12–68% of THg, and the highest value was found at the top of the sulfidic zone, whereas the truly dissolved Hg species (70 ± 9%) dominated in all the rest of the sulfidic zone. MeHg ranged from less than 10% of THg in the oxic mixolimnion to more than 90% in the anoxic monimolimnion. The Hg methylation was most active within the suboxic zone where iron and sulfate reduction are occurring. These results, associated with those of the partition of organic matter (OM), sulfur, and iron, in conjunction with thermodynamic calculations, allow us to present a conceptual scheme for the Hg cycle in the lake. Atmospheric Hg deposited onto surface waters of the lake is partially photo-reduced and returned to the air, another part is scavenged by biogenic particulate matter and conveyed at depth by settling organic material. Water stratification and redox changes create a sequence of reactions from oxic to ferruginous waters where Hg is successively (i) desorbed from particulate OM where mineralization occurs, (ii) adsorbed onto iron-oxy(hydr)oxides, (iii) desorbed where they dissolved, (iv) precipitate as HgS, (v) methylated, and (vi) reduced as Hg0 in the deepest part of the lake. In brief, the (micro)biological uptake, OM, iron and sulfur recycling, through associated microbial consortia, control the Hg cycling in the Pavin waters.

Elimination of Hg (II) in Water by Adsorption through Banana

Banana peel is a low-cost resource that can be used in a wide range of chemical and industrial processes. The novelty of this research is the use of dehydrated and sieved banana peel to remove mercury from water. The main objective of this research is to evaluate the capacity of the banana peel as an adsorbent capable of removing mercury from contaminated water. It has been shown to be an efficient, low-cost, and environmentally friendly process because banana peel is an environmental waste. To determine the ability of the banana peel to adsorb mercury, the following variables were considered: Hg concentration in water (10, 20, 30, 40, 50, 60, 70, 80, 90 and 100 ppb), particle size of the banana peel (100, 150, 200, 250 and 300 microns), quantity of banana peel per 125 ml of solution contaminated with Hg (2 and 5 grams), the contact time was (20, 40 and 60 minutes); it was not necessary to modify the pH of the solutions to obtain high % of mercury removal. The minerals and fatty acids present in the banana peel were also analyzed to improve the interpretation of the adsorption results. A higher adsorption capacity of mercury was perceived with a banana peel sieved at 150 microns; the results are consistent with other research works such as Cd (II) adsorption according to Azarpira et al. [1] where absorption is improved by decreasing the particle size of the filter material. The effectiveness of bioadsorption depends on the initial concentration of mercury ions and the filter material, the particle size of the filter material, the contact time between the mercury ions and the filter material and the pH (although in this project it is not this variable has been intervened). This study demonstrates that the banana peel used as an adsorbent is very efficient and inexpensive for removing mercury from wastewater. It became possible to demonstrate that the amount of Hg adsorbed per unit mass of absorbent increases with increasing initial Hg concentration in contaminated water, as in other metals [1]. The results of this study have confirmed the viability of using banana peel as an effective alternative for removing mercury from mercury-contaminated waters. Future studies will help to evaluate the economic use of this bioadsorbent and the identification of the main active elements it possesses in mercury adsorption. This study will allow a deeper understanding of the mercury absorption process and will verify the potential possibilities of methods to improve the adsorption process.

Pollution and risk assessment of heavy metals in rivers in the antimony capital of Xikuangshan

Xikuangshan (XKS) is the world's largest antimony mining region, and its exploitation for hundreds of years has also resulted in serious soil erosion, fragile ecology, contaminated water, and shortage water. Through systematic and scientific collection samples from the rivers in XKS, the Nemerow index (NI), modified heavy metal pollution index (m-HPI), ecological risk index, and health risk indexeswere used to evaluate and analyze the water quality, pollution levels and risks of heavy metals (Sb, As, Mn, Pb, Zn, Hg, Cd) to ecology and humans in XKS. The results showed that the average concentrations of TN, TP, Sb, As and Hg in surface water were 0.48 mg/L (0–4.34 mg/L), 2.58 mg/L (0–4.34 mg/L), 1.05 mg/L (0.0009–5.33 mg/L), 1.06 mg/L (BDL–19.60 mg/L) and 0.00084 mg/L (LDBL–0.0036 mg/L), respectively, exceeding the limits of the Chinese surface water quality standards. Based on the m-HPI method, only 8.57% of the sampling points are classified as the worst water quality. However, according to the NI method, about 7.14% and 87.16% of the sampling points in the study area are moderately and severely polluted, respectively. The results of heavy metal pollution based on the NI evaluation is were more serious than that on the m-HPI method. The values of ecological risk assessment varied from 22.69 to 7351.20, revealed that heavy metals pose a very serious risk to the surface water ecosystem at more than 50% of the sampling sites, and Sb and As are the main pollutants, followed by Hg. The total non-carcinogenic risk index (TCR) for adults and children were 47.70 and 90.10 respectively, Sb and As is the main non-carcinogenic risk factor. For adults and children, the average carcinogenic risk (CR) of As was 6.49 × 10–3 and 1.05 × 10–2, respectively, and exceeded the threshold of 1 × 10–4, indicating a high carcinogenic risk.

Spatial-temporal variations and pollution risks of mercury in water and sediments of urban lakes in Guangzhou City, South China.

This study aims to investigate the spatial and temporal characteristics, pollution degrees, and potential ecological risks of mercury (Hg) in urban lake waters and sediments in Guangzhou, where is a typical area of Hg emission and population-economic-industrial concentration in South China. In different districts of this city, the water from 15 lakes were collected continuously from June 2020 to May 2021, and the sediments from 9 lakes were collected in 2015 and 2021. The seasonal changes of Hg concentration (Hg-C) in the water were found to be high in winter and low in summer. The spatial distribution of Hg-C in sediments showed that it was high in urban central areas and low in suburbs. The Nemero index and geological accumulation index showed that there were uncontaminated of Hg in the collected lake water, and above moderately contaminated in the lake sediments in urban center, respectively. The Hg pollution potential ecological risk index showed that there was low risk in the collected water, high and extremely high risk in the lake sediments in urban center, respectively. The principal component analysis (PCA) and correlation analysis (CA) of Hg and meteorological factors showed that precipitation, temperature, and vapor pressure had negative effects on the seasonal changes of Hg-C in water, and air pressure and wind direction had positive effects. The PCA and CA of Hg and other geochemical elements showed that anthropogenic emissions may be the main sources of Hg in sediments, which was also supported by the data of population density, road density, and motor vehicles per 1000 people. This study provided a reference for urban lake pollution treatment, resident health, and ecological environment protection.