Source Of Mercury Research Articles

Nano mercury selenide as a source of mercury for rice

Mercury (Hg) is a persistent and toxic metal while mercury selenide (HgSe) is generally considered as the environmental sink of Hg in its biogeochemical cycle. Recent studies found nano-sized HgSe (nano-HgSe) could be transformed by certain bacteria. This raises safety concerns about the application of selenium (Se) to curb Hg contamination in farmlands. Therefore, hydroponic experiments were performed in which rice plants were cultured with different concentrations of nano-HgSe and micro-sized HgSe (micro-HgSe) to explore their bioavailability and toxicity. It was found that both nano-HgSe and micro-HgSe did not affect the germination of rice seeds but affected the growth of rice seedlings. However, nano-HgSe could be more readily absorbed by roots and transferred to the aboveground parts compared to micro-HgSe. The highest Hg and Se levels were found to be 5255.67 ± 2496.14 μg/g and 1743.75 ± 61.87 μg/g, respectively in roots when exposed to 5000 mg/L nano-HgSe. Besides, small portion (1.2%) of methylmercury (MeHg) to total Hg was found accumulated in rice stem when exposed to 100 mg/L nano-HgSe, suggesting that nano-HgSe could be decomposed. Furthermore, nano-HgSe exposure brought oxidative damage to rice with decreased chlorophyll content and GSH-Px activity. In all, nano-HgSe was found to be more absorbable, transportable and methylated in rice plant compared to micro-HgSe. This suggests that although Se application in Hg contaminated farmland is an effective way to reduce the bioavailability of Hg, the risk of the possible remobilization of HgSe should not be neglected. Besides, the finding that nano-HgSe can act as an environmental source of Hg for plants deepens the understanding of biogeochemical cycle of Hg. More works are required to study the factors affecting the formation of nano-HgSe in the environment and the mechanisms of Hg methylation in rice plants after exposure to nano-HgSe.

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.

English

Since the Minamata conference, the scientific and professional worlds (gold industry, metal extraction, health) have come together to conduct research and raise awareness of the effects of mercury (Hg) in the environment, particularly on public health. Africa has not remained on the sidelines of these events, which have a planetary scope due to the long-range transport of various anthropogenic and natural sources of mercury. Since then, scientific data has been produced both in Africa and other continents in the world on the knowledge of the properties of mercury (Hg) as a poison that can migrate through all the links in the food chain. This scientific article is an analysis of mercury (Hg), its sources, its distribution, its health and environmental impacts (terrestrial, aquatic, atmospheric ecosystems, etc.) in Africa. It also aims to present the recent development in this field in the form of a general analysis and to present the measures taken at the political level to control mercury flows in developing countries while highlighting the shortcomings of these policies at the national level in some African countries. Keys words: Mercury, pollution, anthropogenic sources, health effects, Africa.

Mercury sources, contaminations, mercury cycle, detection and treatment techniques: A review

Mercury is considered a toxic pollutant harmful to our human health and the environment. Mercury is highly persistent, volatile and bioaccumulated and enters into the food chain, destroying our ecosystem. The levels of mercury in the water bodies as well as in the atmosphere are affected by anthropogenic and natural activities. In this review, the mercury species as well as the mercury contamination towards water, soil and air are discussed in detail. In addition to that, the sources of mercury and the mercury cycle in the aquatic system are also discussed. The determination of mercury with various methods such as with modified electrodes and nanomaterials was elaborated in brief. The treatment in the removal of mercury such as adsorption, electrooxidation and photocatalysis were explained with recent ideologies and among them, adsorption was considered one of the efficient techniques in terms of cost and mercury removal.

Mercury concentration and speciation in benthic organisms from Isfjorden, Svalbard.

Polar regions are an important part of the global mercury cycle and interesting study sites due to different possible mercury sources. The full understanding of mercury transformations in the Arctic is difficult because this region is the systems in transition -where the effects of the global climate change are the most prominent. Benthic organisms can be valuable bioindicators of heavy metal contamination. In July 2018, selected benthic organisms: macroalgae, brittle stars, sea urchins, gastropods, and starfish were collected in Isfjorden, Spitsbergen. Two of the sampling stations were located inside the fjord system and one at the entrance to the fjord. The results showed that the starfish were the most contaminated with mercury. Total mercury concentrations in these organisms were at least 10 times higher than in other organisms. However, they effectively deal with mercury by transporting it to hard tissue. The dominant form of mercury was the labile form.

The Release and Reduction of Mercury from Solid Fuels through Thermal Treatment Prior to Combustion

The main source of mercury (Hg) anthropogenic emissions is the combustion of hard and lignite coal in power plants. Reduction of Hg emissions from coal-based power production systems involves Hg removal from the fuel before combustion/gasification by thermal treatment (i.e., low-temperature pyrolysis). Herein, we present the results of laboratory and bench-scale studies on Hg removal from coal via thermal fuel treatment. The influence of the process temperature and coal residence time in the reaction zone on Hg removal efficiency and fuel parameters is studied. The properties of the process products are analyzed as follows: proximate and ultimate analysis for solids as well as H2, N2, CO, CO2, CH4, organic compounds C2–C5, density, and HHV for gaseous. The results show a substantial reduction of Hg in the fuel using a low-temperature pyrolysis process. At moderate pyrolysis temperature provided Hg removal efficiencies of up to 50% for hard coal and over 90% for lignite, with a moderate decrease in the chemical enthalpy of the fuel.

Mercury isotopic evidence for the importance of particles as a source of mercury to marine organisms.

The origin of methylmercury in pelagic fish remains unclear, with many unanswered questions regarding the production and degradation of this neurotoxin in the water column. We used mercury (Hg) stable isotope ratios of marine particles and biota to elucidate the cycling of methylmercury prior to incorporation into the marine food web. The Hg isotopic composition of particles, zooplankton, and fish reveals preferential methylation of Hg within small (< 53 µm) marine particles in the upper 400 m of the North Pacific Ocean. Mass-dependent Hg isotope ratios (δ202Hg) recorded in small particles overlap with previously estimated δ202Hg values for methylmercury sources to Pacific and Atlantic Ocean food webs. Particulate compound specific isotope analysis of amino acids (CSIA-AA) yield δ15N values that indicate more-significant microbial decomposition in small particles compared to larger particles. CSIA-AA and Hg isotope data also suggest that large particles (> 53 µm) collected in the equatorial ocean are distinct from small particles and resemble fecal pellets. Additional evidence for Hg methylation within small particles is provided by a statistical mixing model of even mass-independent (Δ200Hg and Δ204Hg) isotope values, which demonstrates that Hg within near-surface marine organisms (0-150 m) originates from a combination of rainfall and marine particles. In contrast, in meso- and upper bathypelagic organisms (200-1,400 m), the majority of Hg originates from marine particles with little input from wet deposition. The occurrence of methylation within marine particles is supported further by a correlation between Δ200Hg and Δ199Hg values, demonstrating greater overlap in the Hg isotopic composition of marine organisms with marine particles than with total gaseous Hg or wet deposition.

Mercury and methylmercury in Baltic Sea sediments, and Polish and Lithuanian soils

We review the current environmental pollution by mercury in the soils of Poland and Lithuania and in the sediments of the Baltic Sea. Mercury is documented to have many negative impacts on the environment as a toxic trace element. In many different chemical forms, it is being released into the environment by both geogenic and anthropogenic activities, with most being released from anthropogenic sources. Methylmercury is considered one of the most toxic forms found in the environment. Mercury levels in sediment and various point sources increased after World War II in the Baltic Sea, which was used as a dumpsite. Previous studies show noticeable differences in total mercury in the Baltic Sea. In the Warta and Odra rivers in Poland, mercury levels are also higher than the background value, though recent findings suggest that river sediments are not the main source of mercury to marine sediments. Concentrations in soils in Poland and Lithuania were below the level of limit values (1 and 1.5 mg/ kg −1 respectively), but Upper Silesia showed concentrations (up to 4.01 mg·kg −1 ) above the limit values. Furthermore, between 1992 and 2006, mercury levels in Wrocław dropped dramatically. The dominant trees in the area can affect mercury accumulation. No data were available for comparison with the soils in Estonia and Latvia.

Optimization and application of passive air sampling method for gaseous elemental mercury in Ulsan, South Korea.

We compared uptake rates and concentrations of gaseous elemental mercury (GEM) by passive sampling conditions and investigated the spatial distribution of GEM in Ulsan, the largest industrial city in South Korea. For the optimization of sampling conditions, two outer sampling containers (cylindrical polyethylene terephthalate and two stainless steel bowls), two different sulfur contents of the sorbent (16.3% and 26.3%), and three sampling periods (1, 2, and 3months) were considered. The uptake rates of GEM were not statistically different by the sampling container, but they were increased with the sulfur contents of activated carbon. A sampling condition using two stainless bowls and lower sulfur contents of activated carbon for 2-3months was preferred with the highest precision of GEM concentrations. With the same method, passive air samples were collected for 3months in duplicate from 10 sites in Ulsan. The concentrations of GEM ranged from 3.13 to 11.2ng/m3 (mean 4.65ng/m3), and the highest concentration was measured at a non-ferrous industrial complex. A zinc smelter in the non-ferrous industrial complex was identified as a major mercury source in Ulsan. This study is the first passive air sampling study investigating the spatial distributions of GEM in different types of industrial areas as well as residential areas of Ulsan.

Editorial: Novel insights into mercury sources and behavior in the surface earth environment

Editorial: Novel insights into mercury sources and behavior in the surface earth environment

Near-global mapping of TGM based on aircraft measurements from intercontinental flights

Atmospheric mercury sources are numerous and complex. Accessing and understanding the strength of each source is important for understanding mercury cycling between the various environmental compartments as it affects atmospheric loadings.In this regard, this study presents an upper tropospheric near-global source evaluation of total gaseous mercury (TGM) and its impacts on atmospheric loadings are therefore examined using TGM measurements from a container aboard intercontinental passenger flights between 2005 and 2016. The trove of measurements performed on board of IAGOS-CARIBIC was exploited through developed receptor models, assuring a high likelihood of extracting the maximal amount of information from the collected data. We reconstructed atmospheric mercury concentrations and assessed the contribution of the major natural and anthropogenic sources, explaining 98% of the observations with a correlation of 82% and a significance level of 0.001 (p-value).The results show that Asia stands out as the main hotspot of TGM, mainly loaded by factors linked to industrial and SO2-related sources. Contribution and geolocation strength of industrial, volcanic, biogenic, biomass burning, and petrogenic-related sources were quantified, identified and presented.The improved data analysis tools as probability mass factorization methods provide additional insights into the nature of the mercury source that can then guide the development of more effective mercury-related management strategies.

Characteristics, Treatment, and Prognosis of Elemental Mercury Intoxication in Children: A Single-Center Retrospective Study.

Mercury exposure is common and can be toxic, especially in children. Children are often drawn to elemental mercury because of its density, color, and proclivity to form beads. We present data on 49 children with mercury intoxication (MI) and 60 children with mercury exposure from Turkey. The most common source of mercury was broken thermometer in schools. Inhaling mercury vapor was the most common route of exposure. The median exposure time was 6 (6-16) hours in the MI group, and the time to 1st symptoms was 10 (0-24) hours. In the MI group, the median blood mercury level was 21 μg/L (13-32.3), the median spot urine mercury level was 40 μg/L (7.66-78), and the median 24-hour urine mercury level was 25.8 μg/L (11-64). The most common symptoms in patients with MI were malaise, muscle pain, muscle cramps, abdominal pain, nausea, headache, and decreased appetite. The patients were treated with n-acetyl cysteine, 2,3-dimercaptopropane sulfonic acid, D-penicillamine, and meso 2,3-dimercaptosuccinic acid. A positive correlation was found between exposure time and urinary mercury level in the MI group (r = 0.793, P < 0.001). A positive moderate correlation was found between exposure time and blood level in the mercury exposure group (r = 0.535, P < 0.00). The neurological and systemic examinations of patients were all normal at the 1st follow-up visit 1 month after discharge. Diagnosis, removal of the exposure source, and use of chelation therapy can result in complete resolution of the signs and symptoms of MI.

Health Remedies as a Source of Lead, Mercury, and Arsenic Exposure, New York City, 2010-2019.

Objectives. To describe the types of health remedies collected during poisoning investigations in New York City over a 10-year period that were found to contain high levels of lead, mercury, or arsenic. Methods. Between 2010 and 2019, the New York City Department of Health and Mental Hygiene collected 584 samples of health remedies during poisoning investigations and store surveys for lead, mercury, or arsenic analysis. Results. There was a significant association between blood lead levels and estimated cumulative daily lead exposures among adult users of rasa shastra Ayurvedic medications. Also, average blood lead levels among adult rasa shastra users were significantly higher than levels among those using other types of non-Ayurvedic health remedies. Conclusions. Rasa shastra Ayurvedic medications can contain very high levels of lead, mercury, and arsenic. This underscores the importance of screening for lead, mercury, and arsenic exposures within at-risk populations. Public Health Implications. The general ease of accessibility to rasa shastra medications raises concerns. There is a need for systemic change that results in primary prevention, that is, removal of the source through policy development and regulatory enforcement in the country of origin. (Am J Public Health. 2022;112(S7):S730-S740. https://doi.org/10.2105/AJPH.2022.306906).

Dispersion of airborne mercury species emitted from the cement plant

The cement industry is the second largest source of anthropogenic mercury (Hg) emissions in Europe, accounting for 11% of global anthropogenic Hg emissions. The main objective of this study was to examine the influence of Hg emissions from the Salonit Anhovo cement plant on Hg levels measured in the ambient air at Vodarna, 1 km downwind from the flue gas chimney. The findings reveal that the plant raw mill operational status plays an important role in Hg concentrations in the flue gas emitted from the plant. Emitted total gaseous mercury was, on average, higher (49.4 μg/m3) when raw mills were in the direct mode (both raw mills-off) and lower (23.4 μg/m3) in the combined mode (both raw mills-on). The average Hg concentrations in Vodarna were 3.14 ng/m3 for gaseous elemental mercury, 53.7 pg/m3 for gaseous oxidised mercury, and 41.9 pg/m3 for particulate bound mercury for the whole measurement period. Atmospheric Hg speciation in Vodarna, coupled with plant emissions and wind data, has revealed that the total gaseous mercury emitted from the cement plant is clearly related to all Hg species measured in Vodarna. Wind blowing from the northeastern quadrant (mostly NE, ENE) is responsible for the elevated Hg levels in Vodarna, where gaseous oxidised mercury levels are highly linked to the cement plant emissions. However, elevated levels of Hg species in the absence of northeastern winds indicate potential inputs from other unknown local sources as well as inputs from regional and global transport mechanisms.

Chemical significance of atmospheric mercury at fishing port compared to urban and suburb in an offshore island

This study explored the chemical significance, spatiotemporal variation, and source origins of atmospheric speciated mercury (ASM) at three contexts (urban, suburb, and fishing port) at the Penghu Islands in the Taiwan Strait. Continuous monitoring of 5-min total gaseous mercury (TGM) was used to determine its hourly, daily, and seasonal concentrations. Manual sampling of 12-h gaseous oxidixed mercury (GOM) and particulate bound mercury (PBM) was used to resolve their diurnal and seasonal variation. ASM further correlated with meteorological parameters and criteria air pollutants. Backward trajectories coped with regional fire maps to identify the potential sources of atmospheric mercury. The yearly mean TGM concentration was about 2.9 times higher than the background level (1.4 ng/m3) of Northern Hemisphere. The highest and lowest seasonal TGM concentration appeared in spring and summer, respectively. Asian continental outflows (ACOs) containing mercury-laden contaminants (MLCs) in spring, while polluted air masses were blown from southern Taiwan where heavily industrial complex had in summer, causing the second highest ASM level. In fall, MLCs emitted from the coastal industrial and urban areas were blown from the Korea Peninsula by Asian Northeastern Monsoons (ANMs). In terms of gas-particle partition, TGM was superior to PBM. Moreover, the highest TGM concentration was observed at the fishing port site, and followed by the suburb and urban sites. High TGM concentration peaks were regularly observed at the fishing port site due to the exhausts of fishing boats.

Pollution Characteristics and Risk Assessments of Mercury in Jiutai, a County Region Thriving on Coal Mining in Northeastern China

Among human activities, coal mining and the combustion of fossil fuels are important sources of mercury in the environment. Research on mercury pollution in coal mining areas and surrounding cities, especially in densely populated areas, has always been at the forefront of this research field. In order to study the characteristics of environmental mercury pollution in small and medium-sized coal mining areas and surrounding towns in China, this study selected the main urban area of Jiutai District, a typical mining town in the Changchun City circle industrial base in northeast China, as the research object. In this study, the geo-accumulation index (Igeo) was used to study the soil mercury pollution degree in Jiutai District, the potential ecological risk index (Er) was used to evaluate the potential ecological risk of soil mercury in the study area, and the human exposure risk assessment model was used to evaluate the non-carcinogenic risk of soil mercury to the human body. The results showed that 32% of the soil samples in the study area had a higher mercury content than the regional soil background value of Jilin Province (0.04 mg·kg−1). According to the Igeo, 19% of the sample sites in the study area were polluted (index &gt; 0). In general, the soil mercury pollution level in Jiutai District is low, and the polluted areas are mainly concentrated in the northeast of the study area. The Er of the soil mercury in the study area ranged from 7.2 to 522.0, with 32% of the sampling sites having a moderate or above potential ecological risk (Er &gt; 40), and the potential ecological risk level of the soil mercury was higher in the northeast of the study area. The non-carcinogenic risk index (HQ) and total non-carcinogenic risk value (HI) of the soil mercury were all far less than 1, indicating that soil mercury pollution in the study area did not harm the health of local adults. The oral ingestion of soil mercury is the main form of human exposure to mercury.

Structural equation modelling of mercury intra-skeletal variability on archaeological human remains

Archaeological burial environments are useful archives to investigate the long-term trends and the behaviour of mercury. In order to understand the relationship between mercury, skeletons and soil, we applied Partial Least Squares - Structural Equation Modelling (PLS-SEM) to a detailed, multisampling (n = 73 bone samples +37 soil samples) design of two archaeological graves dating to the 6th to 7th centuries CE (A Lanzada site, NW Spain). Mercury content was assessed using a DMA-80, and data about bone structure and the grave soil/sediments were obtained using FTIR-ATR spectroscopy. The theoretical model is supported by proxies of bone structure, grave soil/sediments, and location of the bone within the skeleton. The general model explained 61 % of mercury variance. Additionally, Partial Least Square – Prediction Oriented Segmentation (PLS-POS) was also used to check for segmentation in the dataset. POS revealed two group of samples depending on the bone phase (hydroxyapatite or collagen) controlling the Hg content, and the corresponding models explained 86 % and 76 % of Hg variance, respectively. The results suggest that mercury behaviour in the graves is complex, and that mercury concentrations were influenced by i) the ante-mortem status of the bone matrix, related to the weight of each bone phase; ii) post-mortem evolution of bone crystallinity, where bone loses mercury with increasing alteration; and iii) the proximity of the skeletal pieces to mercury target organs, as decomposition and collapse of the thoracic and abdominal soft tissues causes a secondary mercury enrichment in bones from the body trunk during early post-mortem. Skeletons provide a source of mercury to the soil whereas soil/sediments contribute little to skeletal mercury content.

Mercury exposure, neopterin profile, and tryptophan degradation in dental technicians

AbstractAmalgam has been widely used as a restorative dental material for over 150 years. Most standard dental amalgam formulations contain approximately 50% elemental mercury in a mixture of copper, tin, silver, and zinc. Mercury is a highly volatile metal, which can easily vaporize to a colorless and odorless gas. It has been demonstrated that mercury is released from dental amalgam, which is increased by chewing, eating, brushing, and drinking hot liquids. Besides this, amalgam is the main occupational exposure source of mercury for dental workers. It is known that mercury exposure causes immune modulation in humans. In this study, it was aimed to evaluate the changes in neopterin levels and tryptophan (Trp) degradation in dental technicians. It was observed that low levels of occupational mercury exposure resulted in decreased neopterin, kynurenine (Kyn), and Kyn/Trp levels. Moreover, mercury and neopterin levels had a significant positive correlation in workers. The lower neopterin levels and Kyn/Trp in dental technicians compared to an unexposed group indicates a possible immune suppression with low level of occupational mercury exposure during amalgam preparation. The relationship between urinary mercury levels as an indicator of occupational mercury exposure and neopterin reminded an effect on T-cell-mediated immune response.

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.

Mercury Sources and Processes Implied by Other Pollutants Distributions in Surface Water and Sediments of a Subtropical Estuary in Southern China

Mercury Sources and Processes Implied by Other Pollutants Distributions in Surface Water and Sediments of a Subtropical Estuary in Southern China