Search Results (25)

Artisanal and small-scale gold mining (ASGM) poses significant environmental challenges globally, particularly due to mercury (Hg) use. As an example, in Ecuador, Hg use still persists, despite its official ban in 2015. This study investigated the geogenic and anthropogenic contributions of potentially toxic elements (PTEs) in the Ponce Enriquez Mining District (PEMD), a region characterized by hydrothermally altered basaltic bedrock and Au-mineralized quartz veins. To assess local baseline values and identify PTE-bearing minerals, a comprehensive geochemical, mineralogical, and petrographic analysis was conducted on bedrock and mineralized veins. These findings reveal distinct origins for the studied PTEs, which include Hg, As, Cu, Ni, Cr, Co, Sb, Zn, and V. Specifically, Hg concentrations in stream sediments downstream (up to 50 ppm) far exceed natural bedrock levels (0.03–0.707 ppm), unequivocally indicating significant anthropogenic input from gold amalgamation. Furthermore, copper shows elevated concentration primarily linked to gold extraction. Conversely, other elements like As, Ni, Cr, Co, Sb, Zn, and V are primarily exhibited to be naturally abundant in basalts due to the presence of primary mafic minerals and to hydrothermal alterations, with elevated concentrations particularly seen in sulfides like pyrite and arsenopyrite. To distinguish natural geochemical anomalies from mining-related contamination, especially in volcanic terrains, this study utilizes Upper Continental Crust (UCC) normalization and local bedrock baselines. This multi-faceted approach effectively helped to differentiate basalt subgroups and assess natural concentrations, thereby avoiding misinterpretations of naturally elevated element concentrations as mining-related pollution. Crucially, this work establishes a robust local geochemical baseline for the PEMD area, providing a critical framework for accurate environmental risk assessments and sustainable mineral resource management, and informing national environmental quality standards and remediation efforts in Ecuador. It underscores the necessity of evaluating local geology, including inherent mineralization, when defining environmental baselines and understanding the fate of PTEs in mining-impacted environments. Full article

This research quantifies mercury use and models its transport in artisanal and small-scale gold mining (ASGM) in the Lom River during two key periods of intense mining activities and high water flow. Mercury concentrations from mining surfaces were estimated using a soil input function approach. Industrial mercury releases were assessed with a ratio-based approach using official gold production data and the mercury-to-gold ratio. The PEGASE model was applied to simulate mercury transport and pollution in the Lom River and to analyze the pressure–impact relationships of ASGM activities on surface water. Field measurements of the mercury concentrations in the Lom River during the dry and rainy seasons of 2021 were used to validate modeling results. The results indicate that volatilization has a more significant impact on the predicted mercury concentrations than photodissociation. Three scenarios were modeled for mercury use: whole ore amalgamation (WOA), combined whole and concentrate ore amalgamation (WOA + COA), and concentrate ore amalgamation (COA). Mercury use estimates ranged from 2250–7500 kg during intense activity to 1260–4200 kg during high water for the gold production of 750 and 525 kg, respectively. Industrial discharges dominated mercury pollution during the dry season while leaching from mining surfaces was the primary contributor during the rainy season. Full article

Background: Gaseous elemental mercury (Hg⁰ or GEM) is an atmospheric form of mercury (Hg)—a toxic heavy metal—that is naturally released in volcanic environments. Research with wild mice demonstrates that chronic exposure to a hydrothermal volcanic environment leads to the bioaccumulation of Hg in the lungs, but also in both the central (CNS) and peripheric (PNS) nervous systems, with marked indications of neurotoxicity. Studies addressing human exposure to volcanogenic Hg⁰ are scarce, hence its risks are still unknown. This study aims to evaluate the level of exposure to Hg⁰ in children living in a volcanically active environment. Methodology and main findings: Two groups of school-aged children (from 6 to 9 years old) were part of this study: one with children inhabiting a hydrothermal area (exposed group) and another with children inhabiting an area without volcanic activity (non-exposed group). Hair samples were collected from each individual for Hg level analysis. It was found that the levels of Hg in the hair of exposed children were 4.2 times higher than in that of non-exposed children (≈1797.84 ± 454.92 ppb vs. 430.69 ± 66.43 ppb, respectively). Conclusion: Given the vast health risks Hg poses, the need to monitor the health of populations inhabiting volcanically active areas is highlighted. Because little is known about the fate, modifications, and effects of Hg⁰ in the human body, particularly regarding its effects on the nervous system in children, the development of further research within the scope is strongly encouraged. Full article

The use of mercury in gold mining, as well as the presence of uncontrolled and illegal releases to the environment, continues to create severe pollution and public health risks for over 14 million people worldwide, particularly in developing countries. This study presents a modeling framework to estimate the fate and transport of mercury on a national-scale river network, where a physical-based conceptual model is implemented. Using the model, mercury concentrations are estimated for every river segment in the network, serving as a tool for effective management and control nationwide, enabling establishing intervention priorities. To test the framework’s suitability, it was applied to Colombia’s river network, a country with documented mercury pollution issues from gold mining. Results revealed persistent concentrations above 0.001 µg/L in all major basins, and concentrations close to 7 µg/L in active mining areas. The release of nearly 300 mines led to the contamination of river distance between 50 and 285 km downstream, exceeding local drinking water standards. The model results were validated with mercury concentration data of available studies in the country, showing small deviations between modeled and measured concentrations (<0.95 µg/L), confirming the robustness and suitability of the proposed framework as a screening assessment for national-scale mercury transport and fate. Full article

Active biomonitoring of mercury (Hg) using non-indigenous moss bags was performed for the first time within and around the former Hg mining area of Abbadia San Salvatore (Mt. Amiata, central Italy). The purpose was to discern the Hg spatial distribution, identify the most polluted areas, and evaluate the impacts of dry and wet deposition on mosses. The exposed moss bags consisted of a mixture of Sphagnum fuscum and Sphagnum tenellum from an external uncontaminated area. In each site, two different types of moss bags, one uncovered (to account for the wet + dry deposition) and one covered (to evaluate the dry deposition), were exposed. The behavior of arsenic (As) and antimony (Sb) in the mosses was investigated to assess the potential relationship with Hg. GEM (Gaseous Elemental Mercury) concentrations were also measured at the same sites where the mosses were exposed, although only as a reference in the initial stages of biomonitoring. The results revealed that the main Hg emissions sources were associated with the former mining area of Abbadia San Salvatore, in agreement with the measured GEM concentrations, while arsenic and antimony were related to soil enriched in As-Sb waste material. The three elements registered higher concentrations in uncovered mosses with respect to the covered ones, i.e., wet deposition was the key factor for their accumulation on the uncovered mosses, while dry deposition was especially important for the covered samples in the mining area. Hg was accumulated in the mosses via GEM adsorption, uptake of particulate Hg, and precipitation via raindrops/snowfall, with almost no loss and without post-deposition volatilization. The results testified that the chosen biomonitoring technique was an extremely useful tool for understanding Hg transport and fate in a contaminated area. Full article

The aim of this work was to determine the concentrations, distribution, and fate of potentially toxic elements [lead (Pb), zinc (Zn), nickel (Ni), copper (Cu), mercury (Hg), arsenic (As), and cadmium (Cd)] in sediments of a hydropower plant water reservoir located in the Brazilian Cerrado biome (used as system model). The purpose of this study was achieved with an analysis of the level of contamination based on the geoaccumulation index (Igeo) and factor contamination (FC) and comparisons with values established by environmental legislation. The physical–chemical–biological properties of sediment samples, the distribution, and the fate of potentially toxic elements (PTEs) in the basin of the stream studied were also investigated using Pearson’s correlation coefficient (r) and principal component analysis (PCA). Cu, Hg, and Cd concentrations in the sediment samples from most of the points analyzed were above level II of the categorization stipulated in environmental legislation, characterizing sediments of poor quality. Moreover, Igeo and FC values indicated potential pollution of the water reservoir sediment by Cd. Concentrations of Cd exceeding 0.34 mg kg⁻¹ surpassed the reference values for water quality established by Conama Resolution No. 454/2012, highlighting the urgent need for ongoing sediment quality monitoring strategies. Hence, the study water reservoir was classified as being moderately to extremely polluted due to the fate of potentially toxic metals in the sediment samples. Frequent monitoring of the sediment quality in watersheds with hydropower plants is indispensable for the assessment of water resources, considering the importance of the water supply and power generation for the population. Moreover, water contaminated by PTEs poses potential risks to river basins, as well as to human and animal health. The results of this work can assist in the investigation of other water reservoirs around the world. Full article

The Sea of Azov, an inland shelf sea bounding Ukraine and Russia, experiences the effects of ongoing and legacy pollution. One of the main contaminants of concern is the heavy metal mercury (Hg), which is emitted from the regional coal industry, former Hg refineries, and the historic use of mercury-containing pesticides. The aquatic biome acts both as a major sink and source in this cycle, thus meriting an examination of its environmental fate. This study collated existing Hg data for the SoA and the adjacent region to estimate current Hg influxes and cycling in the ecosystem. The mercury-specific model “Hg Environmental Ratios Multimedia Ecosystem Sources” (HERMES), originally developed for Canadian freshwater lakes, was used to estimate anthropogenic emissions to the sea and regional atmospheric Hg concentrations. The computed water and sediment concentrations (6.8 ng/L and 55.7 ng/g dw, respectively) approximate the reported literature values. The ongoing military conflict will increase environmental pollution in the region, thus further intensifying the existing (legacy) anthropogenic pressures. The results of this study provide a first insight into the environmental Hg cycle of the Sea of Azov ecosystem and underline the need for further emission control and remediation efforts to safeguard environmental quality. Full article

The global-scale impacts of mercury discharged from Artisanal Small-scale Gold Mining (ASGM) on soils have been poorly studied, unlike atmospheric emissions. This is a key point to understand the potential exposure to mercury pollution of ecosystems and populations living in the river basins where ASGM is practiced, since the largest fraction of the pollutant is poured into soil, independently of the amalgamation technique employed. ASGM activities emit into the atmosphere mercury in its elemental form, which reacts very slowly with the major oxidants. Therefore, the exact location of the ASGM sites has a limited impact on the atmospheric mercury fate. Conversely, this cannot be applied to the mercury discharged on top of the soil. Two ASGM inventories and the related distributions available in the literature along with two novel distributions based on the intersection of zones characterized by low population density and rural areas were compared using a newly introduced Vulnerability Index. The results from this comparison showed that a precise distribution of ASGM is crucial to effectively evaluate the fate of mercury, and therefore the resulting effects on the local ecosystems. Full article

Owing to various industrial applications of mercury (Hg), its release into the environment at high concentration is becoming a great threat to living organisms on a global scale. Human exposure to Hg is greatly correlated with contamination in the food chain through cereal crops and sea foods. Since Hg is a non-essential component and does not possess a biological role and exhibits carcinogenic and genotoxic behaviour, biomonitoring with a focus on biomagnification of higher living animals and plants is the need of the hour. This review traces the plausible relationship between Hg concentration, chemical form, exposure, bioavailability, bioaccumulation, distribution, and ecotoxicology. The toxicity with molecular mechanisms, oxidative stress (OS), protein alteration, genomic change, and enzymatic disruptions are discussed. In addition, this review also elaborates advanced strategies for reducing Hg contamination such as algal and phytoremediation, biochar application, catalytical oxidation, and immobilization. Furthermore, there are challenges to overcome and future perspectives considering Hg concentrations, biomarkers, and identification through the nature of exposures are recommended. Full article

Gas–particle partitioning between reactive gaseous mercury (RGM) and particle bound mercury (PBM) controls the fates of atmospheric oxidized mercury (namely reactive mercury, RM). We conducted a long-term observations of gaseous elemental mercury (GEM), RGM, PBM, and auxiliary parameters in Chongming Island, Shanghai, China, to understand the characteristics of speciated mercury and their gas–particle partitioning behaviors. The entire average abundances of GEM, RGM and PBM were 2.12 ± 0.94 ng/m³, 14.75 ± 9.94 pg/m³ and 21.81 ± 30.46 pg/m³, respectively. An observation data dependent empirical gas–particle partitioning relationship of partitioning coefficient and temperature log(1/K_P) = −2692.20/T + 10.57 was obtained, and it varied in different season being by the temperature. To further evaluate the influences of temperature, particulate matter (PM), relative humidity on RGM and PBM partitioning process, the particulate fraction (φ = PBM/(PBM + RGM)) was used in this study. High φ values (φ > 0.8) mainly occurred at low temperature domain (<281 K), and high PM concentration enhanced this influence. In addition, high relative humidity shifts RGM from atmosphere partitioning to PBM in response to the diurnal valley φ values at 13:00–16:00 in the summer. Photochemical reactions were proposed to play important roles on partitioning processes between RGM and PBM. This study will benefit for the understanding of oxidized mercury fate and influencing factors in the complex atmospheric pollutants. Full article

Gaseous exchanges of mercury (Hg) at the water–air interface in contaminated sites strongly influence its fate in the environment. In this study, diurnal gaseous Hg exchanges were seasonally evaluated by means of a floating flux chamber in two freshwater environments impacted by anthropogenic sources of Hg, specifically historical mining activity (Solkan Reservoir, Slovenia) and the chlor-alkali industry (Torviscosa dockyard, Italy), and in a pristine site, Cavazzo Lake (Italy). The highest fluxes (21.88 ± 11.55 ng m⁻² h⁻¹) were observed at Solkan, coupled with high dissolved gaseous mercury (DGM) and dissolved Hg (THg_D) concentrations. Conversely, low vertical mixing and saltwater intrusion at Torviscosa limited Hg mobility through the water column, with higher Hg concentrations in the deep layer near the contaminated sediments. Consequently, both DGM and THg_D in surface water were generally lower at Torviscosa than at Solkan, resulting in lower fluxes (19.01 ± 12.65 ng m⁻² h⁻¹). However, at this site, evasion may also be limited by high atmospheric Hg levels related to dispersion of emissions from the nearby chlor-alkali plant. Surprisingly, comparable fluxes (15.56 ± 12.78 ng m⁻² h⁻¹) and Hg levels in water were observed at Cavazzo, suggesting a previously unidentified Hg input (atmospheric depositions or local geology). Overall, at all sites the fluxes were higher in the summer and correlated to incident UV radiation and water temperature due to enhanced photo production and diffusivity of DGM, the concentrations of which roughly followed the same seasonal trend. Full article

Mercury (Hg) pollution in the environment is a global issue and the toxicity of mercury depends on its speciation. Chemical redox reactions of mercury in an aquatic environment greatly impact on Hg evasion to the atmosphere and the methylation of mercury in natural waters. Identifying the abiotic redox pathways of mercury relevant to natural waters is important for predicting the transport and fate of Hg in the environment. The objective of this review is to summarize the current state of knowledge on specific redox reactions of mercury relevant to natural waters at a molecular level. The rate constants and factors affecting them, as well as the mechanistic information of these redox pathways, are discussed in detail. Increasing experimental evidence also implied that the structure of natural organic matter (NOM) play an important role in dark Hg(II) reduction, dark Hg(0) oxidation and Hg(II) photoreduction in the aquatic environment. Significant photooxidation pathways of Hg(0) identified are Hg(0) photooxidation by hydroxyl radical (OH•) and by carbonate radical (CO₃⁻•). Future research needs on improving the understanding of Hg redox cycling in natural waters are also proposed. Full article

Carvone is a monoterpene compound that has been widely used as a pesticide for more than 10 years. However, little is known regarding the fate of carvone, or its degradation products, in the environment. We used GC-MS (gas chromatography–mass spectrometry) to study the fate of carvone and its degradation and photolysis products under different soil and light conditions. We identified and quantified three degradation products of carvone in soil and water samples: dihydrocarvone, dihydrocarveol, and carvone camphor. In soil, dihydrocarveol was produced at very low levels (≤0.067 mg/kg), while dihydrocarvone was produced at much higher levels (≤2.07 mg/kg). In water exposed to differing light conditions, carvone was degraded to carvone camphor. The photolysis rate of carvone camphor under a mercury lamp was faster, but its persistence was lower than under a xenon lamp. The results of this study provide fundamental data to better understand the fate and degradation of carvone and its metabolites in the environment. Full article

Industrial activities have resulted in severe environmental contamination that may expose rural and urban populations to unacceptable health risks. For example, chlor-alkali plants (CAPs) have historically contributed mercury (Hg) contamination in different environmental compartments. One such site (a burden from the Soviet Union) is located in an industrial complex in Pavlodar, Kazakhstan. Earlier studies showed the CAP operating in the second half of the twentieth century caused elevated Hg levels in soil, water, air, and biota. However, follow-up studies with thorough risk characterization are missing. The present study aims to provide a detailed risk characterization based on the data from a recent site assessment around the former CAP. The ⅀HI (hazard index) ranged from 9.30 × 10⁻⁴ to 0.125 (deterministic method) and from 5.19 × 10⁻⁴ to 2.54 × 10⁻² (probabilistic method). The results indicate acceptable excess human health risks from exposure to Hg contamination in the region, i.e., exposure to other Hg sources not considered. Air inhalation and soil ingestion pathways contributed to the highest ⅀HI values (up to 99.9% and 92.0%, respectively). The residential exposure scenario (among four) presented the greatest human health risks, with ⅀HI values ranging from 1.23 × 10⁻² to 0.125. Although the local urban and rural population is exposed to acceptable risks coming from exposure to Hg-contaminated environmental media, an assessment of contamination directly on the former CAP site on the industrial complex could not be performed due to access prohibition. Furthermore, the risks from ingesting contaminated fish were not covered as methyl-Hg was not targeted. An additional assessment may be needed for the scenarios of exposure of workers on the industrial complex and of the local population consuming fish from contaminated Lake Balkyldak. Studies on the fate and transport of Hg in the contaminated ecosystem are also recommended considering Hg methylation and subsequent bioaccumulation in the food chain. Full article

Generally white color of the skin is regarded as a feature of superiority and prettiness around the world. Both the males and females in Pakistan apply skin-lightening creams (SLC) but they do not know about the side-effects of their constituents. Skin-lightening products include SLC and related ointments. The SLC are made by mixing fates and water in standard procedure. Here, 20 SLC specimens were obtained and subjected to mercury, hydroquinone and the total plate count (TPC). The hydroquinone in SLC was determined using HPLC, mercury level was assessed by ICP OES and finally TPC were computing by utilizing nutrient media (Agar). The hydroquinone in SLC ranged from 0 to 7.14 ± 0.18% with a median value of 0.33%. In 25% of the studied samples, hydroquinone was not detected, 70% of the samples showed values within the limit and 5% of the samples (1 sample) had a hydroquinone concentration above the permissible limit defined by Pakistan (5%). The mercury ranged 0-7.7 ppm, with a median value of 2.5 ppm. Mercury was detected in 95% of the samples; thus, only 5% of the samples had no mercury. In turn, 20% had mercury within the limit value while 75% of the samples had concentration above the Pakistan standard limit (1 ppm). Moreover, TPC obtained in this study was less than the allowable value set according to European Union (EU). Hence, the SLC samples showed high concentration of toxic constituents which could cause deleterious skin diseases. Government must monitor such kind of cosmetic products regularly in order to reduce the danger. Full article