Hg Concentrations Research Articles

Heterogeneous effects of Medicaid coverage on cardiovascular risk factors: secondary analysis of randomized controlled trial

ObjectivesTo investigate whether health insurance generated improvements in cardiovascular risk factors (blood pressure and hemoglobin A1c (HbA1c) levels) for identifiable subpopulations, and using machine learning to identify characteristics of people...

Geochemical baseline establishment and accumulation characteristics of soil heavy metals in Sabaochaqu watershed at the source of Yangtze River, Qinghai-Tibet Plateau

The establishment of soil geochemical baseline and heavy metal pollution assessment in the Qinghai-Tibet Plateau is of great significance for guiding environmental management in the high-cold and high-altitude regions. A total of 126 topsoil samples (0–20 cm) were collected and the contents of Cu, Pb, Zn, Ni, Cr, Cd, As and Hg were determined in the Sabaochaqu basin of the Tuotuo River, the source of the Yangtze River, in the Tibetan Plateau. The baseline values of 8 heavy metals were determined by mathematical statistics, iterative 2times standard deviation method, cumulative frequency and reference element standardization, and the soil heavy metal pollution in the study area was assessed by enrichment factor method and pollution index method. The results showed that the average contents of As, Cd, Cr, Cu, Hg, Ni, Pb and Zn were 31.84, 0.29, 66.07, 17.35, 0.021, 27.86, 49.35 and 88.56 mg/kg, respectively. Baseline values were 22.24, 0.217, 64.16, 15.69, 0.0191, 26.46, 34.91, and 68.62 mg/kg, respectively. There is a great difference between the baseline value of soil heavy metals in study area and the Xizang soil background value, especially the baseline value of Cd was 2.68 times of its background value. The results of the pollution evaluation based on the baseline values showed that the 8 heavy metals were slightly enriched, and the overall pollution status was light pollution, and measures should be taken to control and manage them. The research results can provide a reference value for the evaluation of soil heavy metal pollution in the source region of the Yangtze River, and also provide a theoretical basis for the construction of soil heavy metal baseline values in similar high-cold and high-altitude regions.

Spatial variation of mercury contamination in yellow-legged gulls (Larus michahellis) in the Western Mediterranean

Mercury (Hg) is a global pollutant of major concern in marine and coastal environments. In the Mediterranean Sea, Hg concentrations in biota are higher than in other seas, even when seawater concentrations are similar. Seabirds, as marine top predators, can reflect Hg contamination on a large spatial scale. By sampling seabirds at 17 different breeding colonies, we evaluated Hg concentrations of yellow-legged gulls (Larus michahellis) in the occidental Mediterranean basin in 2021 and 2022. More specifically, we investigated spatial variation of Hg contamination in both chicks and adults as well as associated toxicological risks through the use of blood and feathers, which reflect contamination over different periods of the year. The highest concentrations in chicks were found in Djerba (Tunisia) with blood Hg values of (mean ± SD) 1.69 ± 0.51 μg g−1 dry weight (dw). Adults were most contaminated in Djerba and Dragonera (Balearic Islands, Spain) with blood Hg concentrations of respectively 3.78 ± 2.54 and 5.25 ± 3.73 μg g−1 dw. Trophic ecology was investigated using stable isotope analyses (δ13C, δ15N and δ34S as proxies of feeding habitat and diet), and showed that spatial variation in Hg was mainly driven by foraging habitat in both chicks and adults. Low Hg concentrations were related to the use of anthropogenic food sources. An effect of colony location was also found, suggesting spatial differences in local environmental pollution transfer up to seabirds. Our results also supported the use of δ34S to discriminate between marine and continental foraging habitats in generalist seabirds. This study provides new insights onto the spatial distribution of Hg contamination in a widespread seabird, reporting some of the highest Hg values recorded for this species. Populations with highest concentrations are of potential concern regarding toxicological risks.

Trophic stoichiometry of macroelements and metals in a terrestrial food web

In order to understand the transfer of macroelements and toxic metals in the terrestrial food web, barn swallows, terrestrial frogs, and insects were collected from farmlands in the Leizhou Peninsula, and analyzed for macroelements carbon (C), nitrogen (N), phosphorus (P), and sulfur (S) and trace metals nickel (Ni), zinc (Zn), selenium (Se), copper (Cu), chromium (Cr), cadmium (Cd), lead (Pb), and mercury (Hg). The multi-element ecological stoichiometry was discussed to trace the food web flow of nutrients and toxicants. The percentage contents of C, N, P, and S were 35.43–59.91%, 6.89–12.11%, 0.49–4.66%, and 0.44–2.19%, respectively. The concentrations of Ni, Zn, Se, Cu, Cr, Cd, Pb, and Hg were 0.163–116 mg/kg, 38.7–227 mg/kg, 0.0453–3.82 mg/kg, 3.11–141 mg/kg, not detected—79.6 mg/kg, 0.0203–0.358 mg/kg, 0.148–4.57 mg/kg, and 0.00159–1.46 mg/kg, respectively. Organisms at high trophic levels had higher contents of N, P, and S, and lower contents of C. Significant correlations were observed between δ15N and ratios of C: N, C: P, C: S, N: P, N: S, and S: P, indicating selective transfer of biogenic elements for predators in the terrestrial food web. Most metals including Ni, Zn, Se, Cu, Cr, Pb, and Hg had biomagnification factors and trophic magnification factors higher than 1, because the whole body of organisms rather than tissues were used. The negative correlations between the detoxification ratios of Se: X (each toxic metal) and metal concentrations suggest potential adverse effect of metals on terrestrial organisms.

Effective remediation of mercury (II) from aqueous solutions using CS-MnFe2O4-CoS-MWCNTs: Box-Behnken design optimization and adsorption isotherm, kinetics, and thermodynamics evaluation.

Mercury (Hg) is a hazardous heavy metal, non-biodegradable and toxic, posing a serious threat to aquatic life and human health. Therefore, the removal of Hg ions from contaminated water using effective and eco-friendly adsorbents is necessary. In the present study, three magnetic chitosan-based organic-inorganic nanocomposites, such as CS-MnFe2O4, CS-MnFe2O4-CoS, and CS-MnFe2O4-CoS-MWCNTs, were designed and constructed to investigate their capacity for adsorbing Hg ions from aqueous solutions. The physicochemical properties of prepared composites were characterized by various analyses. The BET analyses indicated their high surface area and porous structure, and the N2 adsorption-desorption showed that the modification of CS in three stages by MnFe2O4 and crosslinking reaction, CoS preparation, and MWCNT incorporation resulted in increased N2 adsorption. The XRD confirms the synthesis of MnFe2O4 and CoS in the CS matrix and also the distinct peaks of MWCNTs. The CS-MnFe2O4-CoS-MWCNTs showed acceptable thermal stability with 45% char yields and superparamagnetic properties with magnetic saturation (Ms) of 16 emu g-1. The interactive impacts of independent variables (pH, contact time, and adsorbent dosage) on the removal percentage of Hg(II) onto three prepared adsorbents, as well as the process optimization, were assessed by the Box-Behnken design. The optimum conditions were identified, and the data from the analysis of variance showed that the three independent factors (pH, contact time, and adsorbent dosage) significantly influenced the adsorption of Hg(II). The adsorption isotherm and thermodynamics analysis investigation showed that at low concentrations of Hg(II), the adsorption process was both endothermic and spontaneous for the studied adsorbents.

Mercury enrichments as a paleo-volcanism proxy: Sedimentary bias and a critical analysis across the end-Triassic

Mercury (Hg) anomalies in sedimentary rocks have been increasingly used in paleoclimatology studies for tracing volcanic signals, as Hg emissions from volcanic activity can cause contemporaneous sedimentary Hg enrichment. However, non-volcanic sedimentary controls on Hg have clear potential to mask these signals. These factors include host phase variability linked to environmentally controlled sourcing and settling changes, and/or variable preservation conditions associated with weathering, oxidation and diagenesis. Such factors can limit the efficacy of Hg as a paleo-volcanism proxy. In this study, sedimentary effects on Hg concentration within a complex depositional system in southwest England (St. Audrie's Bay) across the end-Triassic have been analyzed, together with published data from coeval end-Triassic sections globally – an interval of time coeval with the Central Atlantic Magmatic Province (CAMP). Our statistical analysis of Hg and associated geochemical data highlights significant fluctuations in sedimentary Hg due to relative supply differences in Hg and host phases, as well as the changing types and preservation conditions of host phases. End-Triassic sections globally show a consistent undersupply of Hg relative to organic matter across the end-Triassic mass extinction (ETME). To better assess the magnitude and significance of possible Hg enrichments in sedimentary rocks, we present a statistical method for quantifying Hg anomalies to robustly distinguish Hg variations linked to host phase/depositional changes from paleo-volcanism. Our method supports the existence of transient but asynchronous Hg anomalies linked to volcanism from the CAMP across the end-Triassic in most global sections, albeit not in the St. Audrie's Bay section.

Retrieval of chromium and mercury concentrations in agricultural soils: Using spectral information, environmental covariates, or a fusion of both?

The universal contamination of arable land with potentially toxic elements (PTEs) poses a severe threat to food security and jeopardizes worldwide efforts to meet the United Nations Sustainable Development Goals (SDGs). How to obtain more reliable concentrations of PTEs in regional agricultural soils is a priority problem to be solved. Multispectral satellite remote sensing, with its advantages of high spatial and temporal resolution, broad coverage, and low cost, offers the potential to acquire spatial distribution of PTEs in agricultural soils over large areas. However, owing to the complexity of soil environments and the insufficiency of spectral information, the mechanism for retrieving concentrations of PTEs in agricultural soils via multispectral satellites is not yet clear, and the accuracy needs to be improved. In this study, we aimed to assess whether employing a fusion of spectral information and environmental covariates, results in more accurate retrievals of PTEs, specifically chromium (Cr) and mercury (Hg), in croplands than does employing spectral information alone. Three machine learning algorithms—kernel-based support vector machine (SVM), neural network-based back propagation neural network (BPNN), and tree-based extreme gradient boosting (XGBoost)—were developed to retrieve Cr and Hg concentrations in agricultural soils. The results showed that the fusion of spectral information and environmental covariates combined with the XGBoost model performed best in retrieving both Cr and Hg concentrations in agricultural soils with coefficient of determination (R2) values of 0.73 and 0.74, respectively. Environmental covariates were important variables for determining Cr and Hg concentrations in agricultural soils, but the ability to retrieve these element concentrations by utilizing spectral information alone was limited. High Cr concentrations occurred in central towns and southern hilly mountains. High Hg concentrations were detected in the northwestern region and southern hilly mountains. The potential of fusing spectral information and environmental covariates to precisely retrieve PTE concentrations in agricultural soils can serve as a reference for agricultural soil health information monitoring worldwide.

Impact of climatic seasons on the dynamics of carbon, nitrogen and mercury in soils of Brazilian biomes affected by gold mining

Land use change, especially mining activities, contributes to anthropic CO2 emissions, leading to decreased carbon (C) storage and loss of biodiversity. Artisanal gold mining associated with the use of mercury (Hg) for amalgamation may change soil organic matter (SOM) contents, and the release of Hg into the environment generates serious environmental problems. Changes in soil biogeochemistry due to C loss and seasonal climate fluctuations affect Hg dynamics and can either increase or decrease its availability. Therefore, our objective was to evaluate the impact of mining on SOM and Hg geochemistry in four Brazilian biomes. We evaluated the dynamics of C and Hg in the dry and rainy seasons of mining and pasture areas by combining spectroscopic, thermogravimetric, and chemical extraction. The critical role of SOM in Hg retention and the influence of climatic seasons on C and nitrogen (N) stocks were highlighted, along with the availability of Hg in solution. Key findings indicated a 50 % reduction in soil C stocks in mined areas, exacerbated during dry seasons, which also saw up to a 70 % increase in bioavailable Hg. SOM played a critical role in Hg retention, with Hg availability closely linked to soil C stability. These results highlight the environmental degradation linked to mining and suggest strategies to mitigate these impacts by increasing SOM and immobilizing Hg. Amalgamation of gold directly into ore, as in the Amazon, has generated great soil Hg stocks, while Hg availability appeared to be governed by soil C stability. This information can serve as a basis for choosing strategies to mitigate environmental degradation caused by changes in land use in mining activities to promote increase in SOM and to immobilize Hg contents.

Mercury isotope fractionation and mercury source analysis in coal

Understanding the sources of mercury (Hg) in coal is crucial for understanding the natural Hg cycle in the Earth's system, as coal is a natural Hg reservoir. We conducted analyses on the mass-dependent fractionation (MDF), reported as δ202Hg, and mass-independent fractionation (MIF), reported as Δ199Hg, of Hg isotopes among individual Hg species and total Hg (THg) in Chinese coal samples. This data, supplemented by a review of prior research, allowed us to discern the varying trend of THg isotope fractionation with coal THg content. The Hg isotopic composition among identified Hg species in coal manifests notable disparities, with species exhibiting higher thermal stability tending to have heavier δ202Hg values, whereas HgS species typically display the most negative Δ199Hg values. The sources of Hg in coal are predominantly attributed to Hg accumulation from the original plant material and subsequent input from hydrothermal activity. Hg infiltrates peat swamps via vegetation debris, thus acquiring a negative Δ199Hg isotopic signature. Large-scale lithospheric Hg recycling via plate tectonics facilitates the transfer of Hg with a positive Δ199Hg from marine reservoirs to the deep crust. The later-stage hydrothermal input of Hg with a positive Δ199Hg enhances coal Hg content. This process has resulted in an upward trend of Δ199Hg values corresponding with the increase in coal THg content, ultimately leading to near-zero Δ199Hg in high-Hg coals. Coal Hg reservoirs are affected by large-scale natural Hg cycling, which involves the exchange of Hg between continents and seas.

Trace element concentrations and associated human health risk assessment in canned tuna, city of Neyshabur, Iran

Seafood is considered a healthy and nutritious food, but the presence of toxic substances in such foods is a serious problem. The present study aimed to analyze the concentration of some toxic metals in seafood and evaluate their noncarcinogenic risks to consumers. Samples were digested according to the Association of Official Agricultural Chemists (AOAC) standard. The heavy metals concentration of Cd, Ni, Hg, Pb, and Sn in 30 canned tuna samples were determined using an inductively coupled plasma optical emission spectroscopy (ICP-OES). The mean concentrations of Cd, Ni, Sn, Pb, and Hg were 0.7, 0.49, 1.03, 0.31, and 0.12 µg g− 1, respectively. Based on these results, the concentrations of Cd, Sn, and Hg in samples met the required standards. However, the concentrations of Ni and Pb in some samples were higher than the permissible limits. The mean values of Sn, Ni, Pb, Hg, and Cd in samples followed a decreasing order. Since the values of the health risk index for these samples were lower than the HI and HRI risk threshold (<1), they can be consumed without any problems arising. Highlights The metal concentration was measured in the four most popular brands of canned fish sold in Neyshabur City, Iran. Some samples exceeded the maximum permissible level of nickel (Ni) and lead (Pb). A significant correlation was observed between Ni concentration with Pb and Hg concentrations and Pb concentration with Cd concentration. The values of the health risk index (HRI) for noncarcinogenic health risks were lower than 1. The calculated Hazard index (HI) for adult and child consumers was less than 1. The HI values were greater for children than for adults.

Heavy metal contents in water extracts of selected medicinal plants used in the folk medicine of Jordan

BackgroundContamination of medicinal plants with heavy metals from environmental sources may severely impact the quality and safety of botanical products. The consumption of botanicals that are contaminated with heavy metals represents a severe health-threatening danger. Study designThe present toxicological study was conducted to determine the heavy metal concentrations of Cd, Pb, Ni, Cr, Hg, As, and Cu in selected medicinal plants and their water extracts (infusions) of Achillea santolina L., Amygdalus communis L., Artemisia herba-alba Asso., Crataegus aronia L., Viscum cruciatum Sieb., and Nepeta involucrata (Bunge) Bornm. collected from different regions in the south of Jordan, including Birkhdad (site 1), Al-Rashadihya (site 2), and Ain-Lahda (sites 3 and 4). MethodsHeavy metal concentrations in the medicinal herbs and their infusions were determined by Inductively Coupled Plasma Optical Emission Spectrometric Analysis (ICP-OES). The correlation between the content of heavy metals in the studied plants, their water extracts, and the surrounding soil environment was also studied. ResultsHigh concentrations of Ni, Cr, and Cu were detected at all investigated sites of soil. They were in the ranges of 8.46 ± 0.02 to 18.36 ± 0.02 ppm (for Ni), 9.47 ± 0.02 to 24.97 ± 0.06 ppm (for Cr), and 9.53 ± 0.01 to 17.05 ± 1.32 ppm (for Cu), respectively. The high levels of Ni, Cr, and Cu are mainly due to the presence of a highway road that is nearby site 3 and the location of a cement factory that is nearby site 2. The potentially toxic elements of Cd, Pb, and As were non-detectable, and very low concentrations of Hg were observed in the range of 0.17 ± 0.01 to 1.82 ± 0.25 ppm in Artemisia herba-alba collected from all studied locations. High Cu concentrations (20.53 to 23.80 ppm) were detected in A. herba-alba collected from sites 1, 2, and 3 and were higher than the reported normal range of (4 to 15 ppm). On the other hand, the raw materials of all studied plants had low Ni, and Cr concentrations within the range of 0.38 (± 0.01) to 4.05 (± 0.16) ppm and 0.35 (± 0.01) to 2.82 (± 0.01) ppm, respectively. Cd and As were non-detectable in all water extracts of all studied plants. The highest Cu contents were observed in the water extracts of A. herba-alba collected from sites 2 and 3 at concentrations of 64.54 ± 6.41 ppm and 62.43 ± 1.85 ppm, respectively. ConclusionsThe heavy metal contamination in a panel of herbal samples was below the legal limit values, except for those plants harvested close to a highway with heavy traffic or a cement factory. This points to the necessity to selecting suitable locations to culture medicinal plants for therapeutic purposes. We recommend monitoring the herbal quality concerning heavy metal contamination on a routine basis to assure the safety of herbal products for the sake of patients in Jordan and elsewhere.

Atmospheric Mercury Concentrations and Isotopic Compositions Impacted by Typical Anthropogenic Mercury Emissions Sources.

Coal-fired power plants (CFPPs) and cement plants (CPs) are important anthropogenic mercury (Hg) emission sources. Mercury speciation profiles in flue gas are different among these sources, leading to significant variations in local atmospheric Hg deposition. To quantify the impacts of Hg emissions from CFPPs and CPs on local-scale atmospheric Hg deposition, this study determined concentrations and isotopes of ambient gaseous elemental mercury (GEM), particulate-bound mercury (PBM), and precipitation total Hg (THg) at multiple locations with different distances away from a CFPP and a CP. Higher concentrations of GEM and precipitation THg in the CFPP area in summer were caused by higher Hg emission from the CFPP, resulting from higher electricity demand. Higher concentrations of GEM, PBM, and precipitation THg in the CP area in winter compared to those in summer were related to the higher output of cement. Atmospheric Hg concentration peaked near the CFPP and CP and decreased with distance from the plants. Elevated GEM concentration in the CFPP area was due to flue gas Hg0 emissions, and high PBM and precipitation Hg concentrations in the CP area were attributed to divalent Hg emissions. It was estimated that Hg emissions from the CFPP contributed 58.3 ± 20.9 and 52.3 ± 25.9% to local GEM and PBM, respectively, and those from the CP contributed 47.0 ± 16.7 and 60.0 ± 25.9% to local GEM and PBM, respectively. This study demonstrates that speciated Hg from anthropogenic emissions posed distinct impacts on the local atmospheric Hg cycle, indicating that Hg speciation profiles from these sources should be considered for evaluating the effectiveness of emission reduction policies. This study also highlights the Hg isotope as a useful tool for monitoring environmental Hg emissions.

Tree Rings Mercury Controlled by Atmospheric Gaseous Elemental Mercury and Tree Physiology.

Tree rings are an emerging atmospheric mercury (Hg) archive. Questions have arisen, though, regarding their mechanistic controls and reliability. Here, we report contrasting tree-ring Hg records in three collocated conifer species: Norway spruce (Picea abies), Scots pine (Pinus sylvestris), and European larch (Larix decidua), which are from a remote boreal forest. Centennial atmospheric Hg trends at the site, derived from varved lake sediments, peats, and atmospheric monitoring, indicated a steady rise from the 1800s, peaking in the 1970s, and then declining. Prior to ca. 2005, larch and spruce tree rings reproduced the peak in the atmospheric Hg trend, while pine tree rings peaked in the 1930s, likely due to the prolonged sapwood period and ambiguity in the heartwood-sapwood boundary of pine. Since ca. 2005, tree rings from all species showed increasing Hg concentrations in the physiologically active outer rings despite declining atmospheric Hg concentrations. The good agreement between Hg and nitrogen concentrations in active tree-ring cells indicates a similar transport mechanism and cautions against their applicability as atmospheric Hg archives. Our results suggest that tree-ring Hg records are controlled by atmospheric Hg and tree physiology. We provide recommendations for using tree-ring Hg archives that take tree physiology into account.

EVALUATION AND RISK ASSESSMENT OF TRACE METAL IN Solanum aethiopicum GROWN AROUND MECHANIC WORKSHOPS IN UMUAHIA ABIA STATE, NIGERIA.

The careless dumping of waste from automobile workshops has significantly increased the concentration of trace metals in the surrounding environment. This study investigated the health risk assessment associated with Solanum aethiopicum fruit consumption. Soil and Solanum aethiopicum, plant from Umuahia automobile workshop were analyzed for As, Cd, Cr, Cu, Fe, Hg, Li, Ni, Pb and Zn. This was done using Inductively Coupled Plasma Optical Emission Spectrophotometer (ICP-OES), while Hg was analysed using a Cold Vapour Atomic Fluorescence Spectrophotometer (CV-AFS) after acid digestion. The average concentration of As, Cd, Cu, Zn, Fe, Pb, Ni, Hg, Li and Cr in the fruit were 7.16±0.03, 1.68±0.16, 5.03±0.03, 19.45±0.32, 76.21±0.73, 6.23±0.45, 3.87±0.17, 0.0003±0.0001, 0.003±0.001 and 15.35±0.22 mg/kg, respectively. The HRI obtained for Cd was the highest 1.821 while the THQ was 1.82135. Fruit had trace metal concentrations higher than the USEPA, WHO, and FAO's approved permitted standards. Cd, Cr and Pb were determined to be the primary contributing factor linked to the development of health hazards and carcinogenic risk based on the results of the risk assessment. It is therefore appropriate to educate the public on the potential risks associated with consuming garden eggs from Umuahia automobile workshop.

Pollution Characteristics and Source Apportionment of Heavy Metals in Topsoil of Counties Along the Shandong Section of the Yellow River

The 25 counties along the Shandong section of the Yellow River are the core areas for promoting the ecological protection and high-quality development of the Yellow River in Shandong Province. Moreover, it is of great significance to study the current situation, sources, and potential risks of heavy metal pollution in the topsoil in this region. In this study, 103 soil samples were collected from the 25 counties along the Shandong section of the Yellow River, and the contents of eight heavy metals （As, Cu, Pb, Cr, Zn, Ni, Cd, and Hg） were determined. The pollution characteristics of heavy metals were analyzed and evaluated using the geological accumulation index and potential ecological risk index. Correlation analysis and the positive matrix factorization （PMF） model were used to analyze the sources of heavy metals. The results showed that the average contents of Cu and Cr were lower than that of the background values of soils, whereas the average contents of As, Pb, Zn, Ni, Cd, and Hg were 1.16, 1.42, 1.05, 1.14, 2.29, and 1.85 times higher than that of the background values, respectively, and the average contents of all eight elements were lower than the screening value of soil pollution risk in agricultural land. In terms of different heavy metal variations, the coefficient of variation （CV） of Cu and Cd was higher than 0.500, indicating high variations, whereas As, Pb, Cr, Zn, Ni, and Hg showed moderate variation. Cd and Hg were slightly polluted, whereas the other six elements were not polluted. Cd and Hg had a moderate potential ecological risk level, whereas the other six elements were at a low level. Correlation analysis and PMF model showed that the sources of heavy metals in the study area were influenced by four factors, i.e., agricultural activities, natural sources, industrial emissions, and atmospheric dust from coal combustion and vehicle exhaust emissions, and the relative contribution rates were 32.4%, 34.9%, 16.5%, and 16.2%, respectively.

Unexpectedly high wet mercury deposition observed in the Yarlung Tsangpo Grand canyon

Situated in the south edge of the Tibetan Plateau, the Himalayas is expected to receive direct anthropogenic Hg perturbations from South Asia, yet the measurements of atmospheric Hg deposition in the Himalayan region remain scarce. Here we report wet Hg deposition measured in the Yarlung Tsangpo Grand Canyon of the Eastern Himalayas, which is the deepest and longest canyon on earth. The precipitation Hg concentration (56.3 ng L−1) and wet Hg deposition flux (84.7 μg m−2 yr−1) from the Motuo station were observed among the highest ever reported for the Tibetan Plateau. Together with analysis of principal component suggesting Hg was mainly clustered with anthropogenic ions and backward trajectories indicating 88.8% of air masses came from South Asia, our results show that transboudary pollution influences from South Asia could be largely responsible for the unexpectedly high levels of wet Hg deposition. Moreover, the wet Hg flux measurements (84.7 μg m−2 yr−1) are found an order of magnitude (∼13 times) higher than the GEOS-Chem estimates (6.8 μg m−2 yr−1), most likely due to the underestimation of transboundary Hg pollution influence by this model. Our study has important implications for better understanding Hg dynamics and verifying atmospheric Hg models in the Tibetan Plateau and Himalayas region.

Offshore wind farm operation contributed to a slight improvement in seawater quality along the Jiangsu Coast, China

The rapid growth of offshore wind farms (OWFs) is driven by concerns for energy security and climate change mitigation. However, their impact on marine environments remains poorly understood due to limited research. This study analyzes the effects of an OWF along China's Jiangsu Coast on seawater quality using data from different development phases. Results show the major pollutants were different across phases. Heavy metal pollution reached alert levels during construction compared to the safe levels observed in the pre-construction and operational phases, mainly due to increases in Pb, Cd, and Hg concentrations. Eutrophication was mild throughout all periods but exhibited a continuous decrease, primarily attributed to reductions in PH and COD concentrations. As a result, the comprehensive pollution level during construction was increased, but it was improved to a clean level during the operational phase. Besides, significant variations were observed in the spatial distribution patterns of major pollutant indices across different scenarios. These changes may stem from a combination effect of land-based pollution, aquaculture, OWF-induced disturbances to atmosphere and hydrodynamics, OWF-related drain and leakage contamination, and marine management policies. Understanding these effects informs OWF optimization, rational wind resource utilization, and marine ecology protection.

Exposure assessment of pesticide residues, heavy metals, and veterinary drugs through consumption of Egyptian fish samples

Environmental contaminants may enter seafood products either through water and sediments or via feed and feed additives or may be introduced during fish processing and storage. The study focused on the nutritional and toxicological significance of heavy metals, antibiotics, and pesticide residues in 48 fish samples collected from the Kafr-ElSheikh governorate in Egypt. Various analytical instruments are used to determine and detect heavy metals, antibiotics, and pesticides. These include Liquid Chromatography Tandem Mass Spectrometer (LC-MS/MS), Inductively Coupled Plasma Mass Spectrometer (ICP-MS), and Gas Chromatography-Mass Spectrometer (GC-MS). The following metals were discovered in fish species: arsenic (As), cadmium (Cd), cobalt (Co), copper (Cu), iron (Fe), mercury (Hg), manganese (Mn), and zinc (Zn). Each of these metals was detected 47 times. Chromium (Cr) was detected 40 times, nickel (Ni) was detected 27 times, and lead (Pb) was detected 6 times. The mean concentrations of As, Cd, Cr, Co, Cu, Fe, Ni, Mn, Hg, Pb, and Zn were determined to be 0.025, 0.02, 0.501, 0.50, 0.81, 12.56, 0.5, 0.689, 0.051, 0.031, and 5.78 mg/kg, respectively. All levels of cadmium, mercury, and lead detected in fish samples were significantly lower than the maximum permissible limits set by Egyptian and European standards. Furthermore, in this study, antibiotics and pesticide residues were found to be not detected in all analyzed fish samples. Based on the estimated daily intake and hazard quotient values, the concentration levels of metals found in fish samples seem to pose no significant threat to public health.

Impact of inorganic mercury on carotenoids in freshwater algae: Insights from single-cell resonance Raman spectroscopy

The influence of inorganic mercury (Hg(II)) exposure on photosynthetic microorganisms and their pigments remains understudied. Here, we employed resonance Raman (RR) spectroscopy to investigate the responses of two freshwater phytoplankton species, the green alga Chlamydomonas reinhardtii and the diatom Cyclotella meneghiniana to Hg(II) exposure. We selectively recorded the spectral RR signature of carotenoids in intact cells exposed to concentrations of 10 nM and 100 nM of Hg(II), representative for contaminated environment and unexposed control cells. A two-hour exposure of C. reinhardtii resulted in a slight decrease in lutein and β-carotene levels, while total carotenoids RR band broadening, as revealed by the FWHM of the υ1(C=C) stretching mode from averaged RR spectra, suggested conformational changes in pigments. Higher Hg(II) concentration induced more pronounced conformational changes. Similarly, a two-hour exposure of C. meneghiniana resulted in slight decreased level of the fucoxanthin, while diadinoxanthin showed an opposite trend compared to control: when fucoxanthin decreased, diadinoxanthin increased under 10 nM Hg (II) exposure. At higher concentrations, the decrease in fucoxanthin was less pronounced, accompanied by a broadening of the band area, (with FHHM increased), indicating possible conformer occurrence in response to Hg-induced stress. The changes in the main carotenoid species of the two algae are species-specific, Hg(II) concentration-specific, and dependent on exposure time. The calculated spectral differences in absorbances from UV–VIS spectra of methanol extracts from each group supported the main findings obtained by RR, though with caution due to the selective extraction efficiency of the respective carotenoids. This study highlighted for a first time the capability of single-cell RR spectroscopy as a valuable tool for toxicity assessment and for comprehending early-stage alterations in carotenoid metabolism due to toxic metal exposure in vivo.

Distribution characteristics, sources and risk assessment of heavy metals in the surface sediments from the largest tributary of the Lancang River in the Tibet Plateau, China.

Angqu, positioned in the eastern expanse of the Tibet Plateau, claims the title of the largest tributary to the Lancang River. In October and December of 2018, in the sediment of Angqu, a comprehensive investigation was conducted on nine heavy metals-arsenic (As), manganese (Mn), chromium (Cr), cadmium (Cd), lead (Pb), mercury (Hg), copper (Cu), zinc (Zn), and nickel (Ni). This investigation aimed to scrutinize the spatial and temporal distribution patterns of these metals, assess the pollution status and ecological risks associated with the sediments, and delve into the sources contributing to their presence. The research results indicate that the average concentrations of As, Hg, and Cd in Angqu sediments exceed the soil background values of Tibet, while the concentrations of other heavy metals are below the soil background values of Tibet. Notably, arsenic poses potential ecological risks. In Angqu sediments, the concentrations of Mn, Cu, Ni, and Pb are generally higher in the wet season, but the seasonal variations of heavy metals in Angqu sediments are not significant. The sediments in the Angqu Basin are predominantly affected by mercury Hg, Cd, and As, with varying degrees of pollution at different sampling points. In the main stream of Angqu (City section), Hg pollution has reached above a moderate level, whereas As pollution near the tributary is only slightly polluted. The analysis of heavy metal sources reveals that there are five primary contributors to heavy metals in surface sediments of Angqu: parent material, agricultural activities, groundwater, atmospheric deposition, and other unidentified sources. Mn, Cr, Pb, and Ni are mainly derived from soil parent material, accounting for more than 50%. About 60.82% of As comes primarily from groundwater. Zn and Cd are mainly sourced from agricultural activities, accounting for 41.25% and 34.33%, respectively. Additionally, 20.6% of Hg originates from atmospheric deposition.