Toxic Hg Research Articles

Gluten-Free Cereals and Pseudocereals as a Potential Source of Exposure to Toxic Elements among Polish Residents.

Background: Nutritional food quality plays a crucial role in maintaining human health. However, food and drinking water, along with occupational exposure, are the main routes of exposure to toxic elements for humans. The main aim of this study was to determine the content of As, Cd, Pb and Hg in naturally gluten-free grains and products made from buckwheat, millet, maize, quinoa and oat. The safety of consumption of the products tested was also assessed. Methods: The contents of As, Cd and Pb were determined using inductively coupled plasma mass spectrometry (ICP-MS). To measure Hg, an atomic absorption spectrometry method (AAS) with the amalgamation technique was applied. To assess the level of consumption of the tested products, an online survey was conducted. To estimate health risk, three indicators were used: the target hazard quotient (THQ), cancer risk (CR) and hazard index (HI). The research material obtained 242 different samples without replications. Results: The highest average content of As, Cd, Pb and Hg were observed for the following groups of products: oat (10.19 µg/kg), buckwheat (48.35 µg/kg), millet (74.52 µg/kg) and buckwheat (1.37 µg/kg), respectively. For six samples, exceedance of established limits was found—three in the case of Cd and three of Pb. Due to the lack of established limits, As and Hg content of the tested products was not compared. Generally, no increased health risks were identified. Conclusions: Based on the obtained results, the consumption of gluten-free cereals and pseudocereals available on the Polish market seems to be safe. However, there is a great need to establish maximum levels of the toxic elements, especially As and Hg in cereal products in European legislation.

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

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

Differential Detection of Bioavailable Mercury and Cadmium Based on a Robust Dual-Sensing Bacterial Biosensor.

Genetically programmed biosensors have been widely used to monitor bioavailable heavy metal pollutions in terms of their toxicity to living organisms. Most bacterial biosensors were initially designed to detect specific heavy metals such as mercury and cadmium. However, most available biosensors failed to distinguish cadmium from various heavy metals, especially mercury. Integrating diverse sensing elements into a single genetic construct or a single host strain has been demonstrated to quantify several heavy metals simultaneously. In this study, a dual-sensing construct was assembled by employing mercury-responsive regulator (MerR) and cadmium-responsive regulator (CadR) as the separate sensory elements and enhanced fluorescent protein (eGFP) and mCherry red fluorescent protein (mCherry) as the separate reporters. Compared with two corresponding single-sensing bacterial sensors, the dual-sensing bacterial sensor emitted differential double-color fluorescence upon exposure to 0–40 μM toxic Hg(II) and red fluorescence upon exposure to toxic Cd(II) below 200 μM. Bioavailable Hg(II) could be quantitatively determined using double-color fluorescence within a narrow concentration range (0–5 μM). But bioavailable Cd(II) could be quantitatively measured using red fluorescence over a wide concentration range (0–200 μM). The dual-sensing biosensor was applied to detect bioavailable Hg(II) and Cd(II) simultaneously. Significant higher red fluorescence reflected the predominant pollution of Cd(II), and significant higher green fluorescence suggested the predominant pollution of Hg(II). Our findings show that the synergistic application of various sensory modules contributes to an efficient biological device that responds to concurrent heavy metal pollutants in the environment.

Risk assessment of potentially toxic trace elements via consumption of dairy products sold in the city of Yerevan, Armenia

The study aimed to investigate the potentially toxic trace elements (PTEs) Pb, Cd, Hg, Mo, and Cu in dairy products sold in Yerevan's markets and to assess the related exposure and possible health risks among the adult population residing in the capital city of Armenia, Yerevan.The PTEs contents were determined in widely consumed dairy products (pasteurized milk, sour cream, matsoun and cheese from cow milk) using graphite furnace atomic absorption spectrometry. PTE contents were in the range of 7.90E-04 (Pb in pasteurized milk) to 6.75E-01 (Cu in cheese) mg/kg. Food consumption was assessed by the 24-h dietary recall method. The PTE daily intakes and margin of exposure (MOE) were calculated by the deterministic approach.The results indicated potential health concerns for the contribution of dairy products to the overall dietary intake of Pb and Cd. MOEs of Pb and Cd (8.71 and 8.80, respectively) estimated for high consumers of cheese (90 g/day and more) were lower than 10. The pilot data set provides the first comprehensive appraisal on the dairy products contamination by PTEs in the Caucasus region. The results point out further attention to sources of Pb and Cd in Armenian dairy products, including environment and farm characteristics.

ACCUMULATION OF CHEMICAL ELEMENTS BY MEDICINAL PLANTS IN THE NERCHINSK STEPPE (TRANS-BAIKAL TERRITORY)

A number of valuable medicinal plants will grow in the Trans-Baikal Territory, but there is not enough information on the content of chemical elements in them, including vital and toxic ones. The aim of the work was to study the content of chemical elements in medicinal plants in one of the districts of the Trans-Baikal Territory. The concentration of 43 chemical elements in the roots of Saposhnikovia divaricata, Paeonia lactiflora and Phlojodicarpus sibiricus growing in the Nerchinsk steppe (Eastern Transbaikalia) was studied. Soil samples were taken at the plant growth sites to analyze the granulometric composition, pH, content of mobile forms N, P, K, and a number of trace elements. The ecological conditions of the habitat were noted: the height above sea level, the exposure and steepness of the slope, the type and floral composition of the plant community. The roots of the plants, after being released from the ground, were placed in cloth bags and dried. At each site, a mixed sample of 5–15 roots was taken, depending on the weight of the root. Chemical analysis of the soil and plants was carried out in certified laboratories in Moscow. Kostroma and Khabarovsk. In the roots of plants, the concentration of Ti, Cr, Sc, La, Ce, Li, Nb and a number of other elements was found to be high relative to the Clark of terrestrial plants, and the content of Mn, Tl, Se, Cd and other elements was relatively low. The concentration of toxic elements Pb, Cd and Hg did not exceed the MPC in the medicinal raw materials, and the accumulation of As exceeded the MPC in the medicinal raw materials by 4–6 times. The studies conducted in this area were conducted for the first time, they allow us to judge the quality of medicinal raw materials, and in the future, to compare the results with other areas of plant growth.

Sol-Gel Synthesis and Characterization of Highly Selective Poly(N-methyl pyrrole) Stannous(II)Tungstate Nano Composite for Mercury (Hg(II)) Detection

The sol-gel process was used to create a new type of polypyrrole-Stannous(II)tungstate nanocomposite by poly(N-methyl pyrrole (PNMPy) sol in Stannous(II)tungstate gel, produced separately using sodium silicotungstic acid and Tn(II)chloride. Tin(II)tungstate (SnWO3) was made by changing the mixing volume ratios of SnWO3 and with a constant amount of an organic polymer. The composite was characterized by TGA, XRD, FTIR, and SEM measurements. A commercially available glassy carbon electrode (GCE) was modified with PNMPy/nano-Stannous(II)WO3 nanocomposites to create a chemical sensor for selective detection of Hg2+ ions using an effective electrochemical methodology. In the I-V technique, selectively toxic Hg2+ ion was targeted selectively, which shows a rapid reaction toward PNMPy/nano-Stannous(II)WO3/Nafion/GCE sensor. It also demonstrates long-term stability, an ultra-low detection limit, exceptional sensitivity, and excellent reproducibility and repeatability. For 0.1 mM to 1.0 nM aqueous Hg2+ ion solution, a linear calibration plot (r2: 0.9993) was achieved, with a suitable sensitivity value of 2.8241 AM−1 cm−2 and an extraordinarily low detection limit (LOD) of 3.40.1 pM (S/N = 3). As a result, the cationic sensor modified by PNMPy/nano-Stannous(II)WO3/GCE could be a promising electrode.

Probe anchored porous organic polymer monolithic architectures as optical sensor for ultra-trace analysis of Hg2+ in water samples

In this article, we have demonstrated an effective strategy to detect and remove the toxic Hg2+ by an ion-selective optical sensor using chromoionophoric receptor that is homogenously dispersed onto the surface of porous organic polymer (POP) template. Herein, we present a detailed summation of the synthesis of different POPs by employing various kinds of monomers and crosslinkers to discover excellent structural property materials that could cater to the needs of an optical sensor. The resultant POP from the bulk polymerization of N,N-dimethyl allylamine (DMA), and trimethylolpropane triacrylate (TMPTA), i.e., poly(DMA-co-TMPTA), manifested a higher surface area with pore size, thus has been utilized as the substrate material for the fabrication of the sensor. Further, the chromoionophoric coordinating ligand, i.e., 7-4(diethylamino)phenyldiazenyl quinolin-8-ol (DPDQ), is immobilized as receptor molecules onto the POP template for ultra-trace detection of Hg2+. The surface dispersed receptor forms stable 1:1 charge-transfer complexes [Hg2+-DPDQ] with a striking naked-eye color transition from pale orange to bright reddish-brown. The developed optical sensor offers an ultra-fast, selective response for Hg2+ with a lower detection limit of 0.1 μg/L (ppb) in the linear range of 0–100 μg/L. The regeneration of the sensor is envisaged with 0.02 M HCl and can be reused for up to six sensing cycles. Actual water samples from different geographical locations of India are tested using the developed sensor, and the method proved effective for real-time monitoring of Hg2+.

Design of a dual responsive receptor with oxochromane hydrazide moiety to monitor toxic Hg2+ and Cd2+ ions: Usage on real samples and live cells

In this work, we report a facile receptor OMB [N′,N”’-(3-((4-oxochroman-3-yl)methylene)pentane-2,4- diylidene)bis(4-methoxybenzohydrazide)] for the simultaneous detection of toxic analytes (Hg2+ and Cd2+ ions) in environment and biological samples. The receptor OMB exhibits an excellent selectivity and sensitivity which was determined using absorption and emission spectra. The receptor OMB shows rapid detection with lowest LOD (0.62 nM for Hg2+ ions and 0.77 nM for Cd2+ ions) and LOQ (2.08 nM for Hg2+ ions and 2.57 nM for Cd2+ ions) values. In addition, the receptor OMB exhibits 1:1 binding stoichiometry towards Hg2+ and Cd2+ ions with binding constant values of 5.5 × 106 M−1 and 4.6 × 106 M−1. Moreover, the synthesized receptor OMB possess ability to detect these analytes (Hg2+ and Cd2+ ions) in realistic samples (food and water) which was recognized using photoluminescence spectroscopy technique. In addition, the receptor OMB is also utilized to detect both the analytes in live HeLa cells. Thus, the overall results indicate that the receptor OMB was more suitable to detect the toxic analytes (Hg2+ and Cd2+ ions) present in the environment.

Triazine-Based Functionalized Activated Carbon Prepared from Water Hyacinth for the Removal of Hg2+, Pb2+, and Cd2+ Ions from Water.

A novel chelating adsorbent, based on the functionalization of activated carbon (AC) derived from water hyacinth (WH) with melamine thiourea (MT) to form melamine thiourea-modified activated carbon (MT-MAC), is used for the effective removal of Hg2+, Pb2+, and Cd2+ from aqueous solution. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET) theory confirm the successful functionalization of AC with the melamine thiourea chelating ligand through the amidation reaction between the carboxyl groups of oxidized activated carbon (OAC) and the amino groups of melamine thiourea (MT) in the presence of dicyclohexylcarbodiimide (DCC) as a coupling agent. The prepared MT-MAC exhibited extensive potential for the adsorption of the toxic metal ions Hg2+, Pb2+, and Cd2+ from wastewater. The MT-MAC showed high capacities for the adsorption of Hg2+ (292.6 mg·g–1), Pb2+ (237.4 mg·g–1), and Cd2+ (97.9 mg·g–1) from aqueous solution. Additionally, 100% removal efficiency of Hg2+ at pH 5.5 was observed at very low initial concentrations (25–1000 ppb).The experimental sorption data could be fitted well with the Langmuir isotherm model, suggesting a monolayer adsorption behavior. The kinetic data of the chemisorption mechanism realized by the melamine thiourea groups grafted onto the activated carbon surface have a perfect match with the pseudo-second-order (PSO) kinetic model. In a mixed solution of metal ions containing 50 ppm of each ion, MT-MAC showed a removal of 97.0% Hg2+, 68% Pb2+, 45.0% Cd2+, 17.0% Cu2+, 7.0% Ni2+, and 5.0% Zn2+. Consequently, MT-MAC has exceptional selectivity for Hg2+ ions from the mixed metal ion solutions. The MT-MAC adsorbent showed high stability even after three adsorption–desorption cycles. According to the results obtained, the use of the MT-MAC adsorbent for the adsorption of Pb2+, Hg2+, and Cd2+ metal ions from polluted water is promising.

Potentially toxic elements and microplastics in muscle tissues of different marine species from the Persian Gulf: Levels, associated risks, and trophic transfer

Selected potentially toxic elements (PTEs), including As, Cd, Co, Cr, Cu, Hg, Ni, Pb, Se, and Zn, along with microplastic particles (MPs) were characterized in the muscle of seafood species in order to study potential health risk and also investigate biomagnification of the contaminants. The results revealed high levels of the analyzed PTEs and MPs in crustaceans. The cancer risk among the consumer population (adult and children) posed by As is higher than the acceptable lifetime risk of 10−4. Portunus plagicus and Platycephalus indicus had the highest and lowest amount of MP particles in their muscles, respectively, among investigated species. Finally, PTEs (except Hg) and MPs are not biomagnified in the collected species. The results of this research emphasize the importance of accounting for health risks posed by potential pollutants via consumption of contaminated seafood.

New Eco-Sustainable Feed in Aquaculture: Influence of Insect-Based Diets on the Content of Potentially Toxic Elements in the Experimental Model Zebrafish (Danio rerio).

According to the concept of circular economy, insects represent good candidates as aquafeed ingredients. Nevertheless, there are some potential chemical risks linked with insect consumption. In this study, we reared the teleost Danio rerio, used as an experimental model, with five experimental diets characterized by increasing levels (0%, 25%, 50%, 75%, and 100%) of full-fat Hermetia illucens (Hi) prepupae, substituting for fish meal (FM) and fish oil (FO). We investigated the presence of potentially toxic elements (PTEs) Cd, Pb, Ni, As, and Hg in larval (20 days), juvenile (2 months), and adult (6 months) fish. Quantitative determinations of Cd, Pb, Ni, and As were made with an atomic absorption spectrometer; the total mercury content was determined by a direct mercury analyzer. The substitution of FM and FO with Hermetia illucens meal led to a reduction in the content of some PTEs, such as Pb, As, and Ni, in fishfeed, leading to concentrations below the legal limit of undesirable substances in animal feed. By increasing the Hi meal dietary content, we observed in the Danio rerio specimens an increase in Cd, Pb, and Ni content and a reduction in As content for all life stages. Moreover, a general increase in the content of Cd, Pb, Hg, and Ni from larvae to juvenile was measured, while the shift of Danio rerio from the juvenile to the adult stage involved a significant increase in the content of Pb, Hg, and Ni. Larvae had a reduced ability to bioaccumulate metal(loid)s compared to juveniles and adults. In conclusion, the content of PTEs in Danio rerio is influenced both by the type of diet administered and by the life stage of the animal itself. This research demonstrates the possibility of using Hi prepupae as an aquafeed ingredient without exposing fish to a chemical risk and, in perspective, allows applying these eco-sustainable diets for the breeding of edible fish species, without endangering human health.

Demand-oriented construction of Mo3S13-LDH: A versatile scavenger for highly selective and efficient removal of toxic Ag(I), Hg(II), As(III), and Cr(VI) from water

Inspired by the classic ion-exchange reaction, a single phase material of Mg0.66Al0.34(OH)2(Mo3S13)0.03(NO3)0.14(CO3)0.07·H2O (Mo3S13-LDH) was masterly constructed by intercalating Mo3S132− into the MgAl-LDH gallery. Prepared Mo3S13-LDH displays excellent binding affinity and high selectivity for Ag(I) and Hg(II) in a mixed solution, in which an apparent selectivity order of Hg(II) > Ag(I) ≫ Pb(II), Cu(II), Ni(II), Co(II), Cd(II), and Mn(II) is observed. Enormous capture capacities (qmAg = 446.4 mg/g, qmHg = 354.6 mg/g) and fast equilibration time (within 60 min) place Mo3S13-LDH in the upper ranks of materials for such removal. For oxoanions, As(III) (HAsO32−) and Cr(VI) (CrO42−) can be specifically trapped by Mo3S13-LDH with comparable loading ability (qmAs = 61.8 mg/g, qmCr = 90.6 mg/g) in the coexistence of multiple interfering anions. Notably, high Hg(II) and Cr(VI) concentrations are finally reduced below the safe limit of drinking water. The excellent capture capacity of Mo3S13-LDH benefits from the rational design by following two aspects: (i) the multiple sulfur ligands in Mo3S132− groups give place to various capture modes and different affinity orders for target ions, and (ii) large-sized Mo3S132− groups widen the interlayer spacing of LDH, thereby accelerating the mass transfer process. Furthermore, the satisfactory structural stability of Mo3S13-LDH is also reflected through the unchanged hexagonal prismatic shape after adsorption. All of these highlight the great potential of Mo3S13-LDH for the application in water remediation.

Synthesis of sulfonamide based chemosensor for sensing of toxic Hg2+ ions in soil extract

Schiff base (3) was synthesized through single step condensation of sulfanilamide and isatin and characterized with 1H NMR, 13C NMR, FT-IR and mass spectrometry analysis. The probe (3) was evaluated as the fluorometric and colorimetric sensor for toxic Hg2+ ions in semi aqueous medium. The LOD and LOQ were found to be 110 and 368 nM, respectively for Hg2+ ions. Binding stoichiometry of the (3):[Hg2+] was establised to be 1:1 (with B-H and Job’s plot), which was also supported by mass spectrometry. Computational studies (TD-DFT) further confirmed the complexation of the (3) and Hg2+ ions with UPBEPBE/6-311G (d.p) level of theory. Finally recuperation studies of probe (3) were carried out with the help of EDTA and showed reusability of (3) upto 6 cycles. Also these studies assist to develp a INHIBIT molecular logic gate. The probe (3) was practically used against spiked soil extract samples and resulted good amount of recovery.

A dual-functional chemosensor based on phenazine derivative for detecting toxic ions in water samples and cosmetic

ABSTRACT Selective monitoring and targeted identification of various noxious ions have received significant attention in biology, industry and environments. Herein, we developed an easily available colorimetric and fluorescence sensor (PZ) based on phenazine derivative, successfully achieving the discriminative detection of Hg2+ and CN− ions. Compared with other interfering ions, PZ had high sensitivity and specificity towards Hg2+ and CN−. The lowest limits of Hg2+ and CN- by PZ were 1.52 × 10−8 M and 7.05 × 10−7 M, respectively. Significantly, this chemosensor PZ allowed visual monitoring of toxic Hg2+ and CN− ions in a few seconds, presenting a great potential in the practical application (skin-whitening cosmetic, water samples, and nutlet). Such an effective strategy is expected to offer some guidance for distinguishing the identification of toxic ions in optical sensing.

Содержание микроэлементов в дальневосточной мойве Mallotus catervarius (Pisces: Osmeridae) из прибрежных вод юго-западной части о. Сахалин

The content of Fe, As, Cu, Mn, Cr, Ni, Pb, Hg and Cd in the muscles and gonads of the Pacific capelin sampled in 2020 in the coastal waters of the southwestern part of Sakhalin Island was estimated. The highest content of As is noted in muscles, Mn – in fish eggs, Hg – in muscles and milt. The content of trace elements in fish muscles and gonads decreases in the range Fe – Cd or Hg. The concentrations of normalized toxic elements Pb, Cd, As and Hg in the muscles and gonads of the Pacific capelin are safe according to hygienic requirements for food products. The data obtained indirectly indicate a favorable ecological situation in terms of the content of normalized toxic elements in the waters near southwest Sakhalin.

Open questions on toxic heavy metals Cd, Hg and Pb binding small components of DNA and nucleobases. Are there any predictable trends?

In this perspective article, we provide a bibliographic compilation of experimental and theoretical work on Cd, Hg, and Pb, and analyze in detail the bonding of M2+ and CH3M+ (M = Zn, Cd, Hg, Pb) with urea and thiourea as suitable models for larger biochemical bases. Through the use of DFT calculations, we have found that although in principle binding energies decrease according to ionic size (Zn2+ > Cd2+ > Pb2+), Hg2+ largely breaks the trend. Through the use of EDA (Energy Decomposition Analysis) it is possible to explain this behavior, which is essentially due to the strong contribution of polarization to the binding. This conclusion is ratified by the NEDA (Natural Energy Decomposition Analysis) formalism, showing that the charge transfer term is very large in all cases, but particularly in the case of the mercury-thiourea system. The general trends observed for the interactions with CH3M+ monocations show however CH3Hg+ binding energies systematically smaller than the CH3Zn+ ones, likely because the relativistic contraction of the Hg orbitals is very much attenuated by the attachment to the methyl group. Finally, we have investigated the gas-phase reactivity between EtHg+ and uracil to compare it with that exhibited by CH3Hg+ and n-ButHg+ previously described in the literature. This comparison gathers new information that highlights the importance of the length of the alkyl chain attached to the metal on the mechanisms of these reactions. For methyl mercury, only the alkyl transfer process is allowed; for butyl mercury, protonation is clearly favored, and for ethyl mercury, both paths are competitive experimentally.

Hybrid photoluminescent material from lanthanide fluoride and graphene oxide with strong luminescence intensity as a chemical sensor for mercury ions

In this work, we employed NaxLiyGdF4:Tb3+@PMA@Phen@GO nanocomposite as chemical sensor for selective and sensitive luminescence sensing of toxic Hg2+ metal ion.

Plasmonic Gold Nanoparticles Stain Hydrogels for the Portable and High-Throughput Monitoring of Mercury Ions.

The hybrid of l-cysteine and agarose can reduce HAuCl4 and support the rapid growth of plasmonic gold nanoparticles (Au NPs) in the hydrogel phase. The l-cysteine-doped agarose hydrogel (C-AGH) not only offers the substrate the capacity to reduce Au(III) ions but also stabilizes and precisely modulates the in situ grown Au NPs with high repeatability, easy operation, and anti-interference performance. Herein, before the incubation of HAuCl4, the improved hydrogel is preincubated in the aqueous solution containing mercury ions, and the cysteine can specifically conjugate with mercury via the thiol groups. Subsequently, the responsive allochroic bands from dark blue to red can be identified in the solid hydrogel after the incubation of HAuCl4, which is attributed to the formation of regulated Au-Hg nanoamalgams. As a proof-of-concept, toxic Hg2+ ions are exploited as targets for constructing novel sensing assays based on the improved C-AGH protocol. Based on naked-eye recognition, Hg2+ could be rapidly and simply measured. Additionally, the high-throughput and trace analysis with a low limit of detection (3.7 nM) is performed using a microplate reader. On the basis of the filtering technique and remodeling of hydrogels, C-AGH working as the filtering membrane can even achieve the integration of enrichment and measurement with enhanced sensitivity. Significantly, the strategy of using an allochroic hydrogel with the staining of Au NPs can promote the rapid and primary assessment of water quality in environmental analysis.

Risk Assessment of Contaminants in Sewage Sludge Applied on Norwegian Soils

Risk Assessment of Contaminants in Sewage Sludge Applied on Norwegian Soils

Ecological risk of heavy metals in lake sediments of China: A national-scale integrated analysis

Intensive anthropogenic activities, specifically, industrial and agricultural production, have resulted in heavy metal enrichment in lake sediment and threats to aquatic ecosystems and human health. Evaluating the potential ecological risk of heavy metals in lake sediment is essential for promoting appropriate lake management in aquatic ecosystems. Large-spatial scale risk evaluations of heavy metal pollution in lake sediment in densely populated countries such as China are lacking. We compiled sediment heavy metal (Cu, Pb, Zn, Ni, Cr, As, Hg, and Cd) data from 190 lakes distributed across five geographic zones in China published between 2000 and 2019, evaluated the potential ecological risk and identified heavy metal sources through positive matrix factorization. Five conclusions were drawn. (1) Regarding the eight collected heavy metals, 6.1–40.4% of 190 lakes exhibited higher concentrations than the Chinese soil background value, and the concentration in 6.2% of lakes exceeded the probable effect concentration. (2) Based on the potential ecological risk index (PERI) and sum of toxic units (STU), Cd and Hg were the major pollutants. (3) The PERI value notably decreased with increasing lake surface area, and small lakes (<10 km2) generally yielded high PERI values. Among the five Chinese geographic zones, the Eastern Plain Lake Zone and Inner Mongolia-Xinjiang Lake Zone exhibited higher potential ecological risk. Compared to natural lakes, urban lakes and reservoirs posed higher ecological risks, while freshwater lakes yielded higher PERI values than saltwater lakes and saline lakes. (4) In all lakes, lake sediment pollutants Cu and Zn mainly originated from traffic sources; Cd originated from agricultural activities; Pb and Hg were related to industrial activities; and Ni, Cr and As indicated mixed sources. (5) In the Eastern Plain Lake Zone, Yunnan-Guizhou Plateau Lake Zone and Northeast Plain and Mountain Lake Zone, industry was the dominant source of heavy metals in lake sediment, while in the Tibetan Plateau Lake Zone and Inner Mongolia-Xinjiang Lake Zone, except for industrial sources, agricultural sources played an important role. Our national-scale integrated analysis provides valuable references for both macroscale policy formulation and polluted lake restoration.