Toxic Hg Research Articles

A Review on Pyridine Based Colorimetric and Fluorometric Chemosensor for Detection of Hg2+ ion.

Pyridine, N-containing heterocyclic organic compound, displays strong coordination capabilities with various metal ions. It can be synthesized through various methods, such as Friedlander synthesis, heterocumulene synthesis, cross-coupling reactions, the Radziszewski reaction, Bonnemann cyclization, as well as cobalt-catalyzed synthesis. Experimental and spectroscopic analyses have demonstrated a strong binding affinity between pyridine and several heavy metal ions, including Pb2+, Hg2+, and Cd2+ ions. The escalating environmental pollution caused by the disposal of heavy metal ions in rivers, open air, and water reservoirs poses a significant threat to both ecosystem and human health. To address these environmental challenges, a cost-effective and easily synthesized chemosensor has been prepared for identifying toxic heavy metal ions in various samples. Pyridine's photophysical properties make it an effective sensor for detecting Hg2+ ions, displaying fluorescence quenching or enhancement in their presence. The coordination between pyridine and Hg2+ ions lead to shifts in the absorption spectra. The pyridine-based sensor has been evaluated for its sensitivity, selectivity, and detection limits under different experimental conditions. Pyridine's solubility and environmental stability make it applicable for real-time detection, making pyridine probes valuable tool for monitoring toxic Hg2+ ions in the environment. The results demonstrate that the pyridine-based chemosensor exhibits good selectivity and sensitivity for targeting Hg2+ ions, with detection limits within acceptable ranges. This review (from years 2011 to 2023) emphasizes the preparation of various substituted pyridine compounds as selective, sensitive, and specific sensors for real-time detection of Hg2+ ions.

Assessment of Gold and Mercury Losses in an Artisanal Gold Mining Site in Nigeria and Its Implication on the Local Economy and the Environment

The objective of this work was to establish the gold and mercury losses in an artisanal mining deposit (Uke) in Nigeria to convince miners about their inefficiency and suggest changes in their gold extraction practices. Samples of feeds and tailings from five sluice box concentration processes previously ground in hammer mills below 1 mm (P80 = 0.5 mm) were systematically sampled every 15 min. for 4 h and sent for gold analyses by a fire assay and intensive cyanidation. Dry grain size analyses of primary and amalgamation tailings allowed us to find out in which size fraction gold and mercury are lost. Total mercury losses in sixteen operations were obtained by weighing mercury at the beginning and in all steps of the concentrates’ amalgamation. After analyses, the average gold grade in the feed resulted in 3.80 ± 1.52 ppm (two standard deviations). The gold recovery was 29.24 ± 13.24%, which is low due to a lack of liberation of the fine gold particles from the gangue (silicates). Finer grinding would be necessary. The mercury balance revealed that 42% of the mercury added is lost, in which 26% involves tailings and 16% evaporated. The HgLost-to-AuProduced ratio was found to be 3.35 ± 9.46, which is exceedingly high for this type of amalgamation process that should have this ratio around 1. One reason is the excessive amount of mercury in the amalgams, 76.5 ± 38.12%, when the normal is around 40%–50%. Mercury lost by evaporation in open bonfires is clearly contaminating amalgamation operators (usually children), neighbours, and the environment. The Hg-contaminated tailings and primary tailings are sold to local cyanidation plants, and this can form toxic soluble Hg(CN)2 in the process. The results of this research were brought to the attention of the miners and other stakeholders, including the regulatory agencies of the government. The % gold recovery by amalgamation was established in this study, but if this process recovers 50 to 60% of the liberated gold particles in a concentrate and 30% of gold was recovered in the sluice boxes, then the total gold recovery should be between 15 and 20; i.e., 80 to 85% of gold mined is lost. On average, an operation produces 8.26 g of gold/month, which is split to six miners, representing USD 69/month/miner or USD 2.3/day. It was discussed with miners, authorities, and community members (in particular female miners) how to avoid exposure to mercury, how to improve gold recovery without mercury, and the health and environmental effects of this pollutant.

Anthraquinone Schiff base and SDS-based visual detection for environmental safety: Targeting triphosgene and Hg2+ with secondary focus on detection of BSA

New sensing techniques with exceptional performance, i.e., high sensitivity, high selectivity, and dependability, are needed to meet the growing demand for quick and accurate environmental pollution prevention and monitoring. A novel Schiff base probe synthesized from anthraquinone and 4-(diethylamino)-2-hydroxybenzaldehyde (coded as AQHB) was synthesized and subsequently combined with anionic surfactant Sodium dodecyl sulfate (SDS) assemblies to form highly fluorescent AQHB@SDS ensemble. The zeta potential of ensemble AQHB@SDS is −52.6 mV confirm the encapsulation of AQHB (-17.3 mV) in SDS micelles. This formed fluorescent AQHB@SDS ensemble further practical applications in detection of toxic triphosgene and Hg2+ ions via naked eye color change and fluorescence quenching mechanism. The fluorescence of in-situ formed AQHB@SDS+Hg2+ complex restored by the addition of BSA. The optimized system demonstrates detection limits of 0.60, 0.68, and an impressive 0.028 nM for triphosgene, Hg2+, BSA respectively. Control experiments revealed that the -OH and -NH groups in AQHB along with anionic surfactant played crucial roles in the sensing mechanism. Moreover, the ensemble AQHB@SDS system efficiently detected triphosgene and Hg2+ in real samples, such as water and soil, highlighting its practical applicability.

Overexpression of bacterial γ-glutamylcysteine synthetase increases toxic metal(loid)s tolerance and accumulation in Crambe abyssinica.

Transgenic Crambe abyssinica lines overexpressing γ-ECS significantly enhance tolerance to and accumulation of toxic metal(loid)s, improving phytoremediation potential and offering an effective solution for contaminated soil management. Phytoremediation is an attractive environmental-friendly technology to remove metal(loid)s from contaminated soils and water. However, tolerance to toxic metals in plants is a critical limiting factor. Transgenic Crambe abyssinica lines were developed that overexpress the bacterial γ-glutamylcysteine synthetase (γ-ECS) gene to increase the levels of non-protein thiol peptides such as γ-glutamylcysteine (γ-EC), glutathione (GSH), and phytochelatins (PCs) that mediate metal(loid)s detoxification. The present study investigated the effect of γ-ECS overexpression on the tolerance to and accumulation of toxic As, Cd, Pb, Hg, and Cr supplied individually or as a mixture of metals. Compared to wild-type plants, γ-ECS transgenics (γ-ECS1-8 and γ-ECS16-5) exhibited a significantly higher capacity to tolerate and accumulate these elements in aboveground tissues, i.e., 76-154% As, 200-254% Cd, 37-48% Hg, 26-69% Pb, and 39-46% Cr, when supplied individually. This is attributable to enhanced production of GSH (82-159% and 75-87%) and PC2 (27-33% and 37-65%) as compared to WT plants under AsV and Cd exposure, respectively. The levels of Cys and γ-EC were also increased by 56-67% and 450-794% in the overexpression lines compared to WT plants under non-stress conditions, respectively. This likely enhanced the metabolic pathway associated with GSH biosynthesis, leading to the ultimate synthesis of PCs, which detoxify toxic metal(loid)s through chelation. These findings demonstrate that γ-ECS overexpressing Crambe lines can be used for the enhanced phytoremediation of toxic metals and metalloids from contaminated soils.

Assessment of Essential and Toxic Element Levels in the Toenails of Children with Autism Spectrum Disorder.

Autism spectrum disorder (ASD) has become a global public health concern, impacting the quality of life. The question of gene-environment interaction in the emergence of ASD remains a subject of ongoing debate, and exploring its pathophysiology is thoroughly related to metals as a risk factor. Therefore, this study aims to assess the levels of toxic (Al, Cd, Hg, and Pb) and essential (Cr, Mn, Fe, Ni, Cu, Zn, and Se) elements in toenail samples collected in children with ASD and neurotypical children, by ICP-MS. Parallelly, we will discuss the use of toenails as an exposure indicator. The study involved 208 children aged 3 to 14 from Marrakech, Morocco. One hundred two were diagnosed with ASD and 106 were neurotypical children. Significant statistical differences in the concentration of Cr, Mn, and Fe were documented between the two groups. Higher levels of Pb in toenails compared to reference values have been reported. No association was established between concentrations of elements and age. Spearman correlation coefficients revealed a significantly different pattern of mutual dependence for toxic and essential elements between the two groups. The strongest positive correlations were found in the neurotypical group (Fe-Mn (ρ = 0.750), and Se-Zn (ρ = 0.800)). These results provide additional, although inconclusive, evidence on the probable role of element disturbance in the pathogenesis of ASD. Further studies should be performed to explore other nutritional, cultural, sociodemographic, environmental, and methodological factors that may impact the levels of these elements in the nails and their possible correlation with the incidence of ASD.

Association "neurotoxicity" of Toxic Metal Mercury in Hair with Autism Spectrum Disorders in Children

Autism spectrum disorder is a complicated neurological disease that is identified by the occurrence of two defining characteristics present in people with ASD, notably social deficits and repetitive and stereotypical behaviors. This review aims to systematically investigate the relationship between the levels of toxic and trace element Hg in hair and the developments of ASD.. The objective of this review is to Methodically investigate the connection Amidst ASD" emergence, also" hair' levels of hazardous, also trace elements Hg.. Through Original articles that reported on the amounts of trace elements Hair was incorporated. The majority of studies' interests change grave not harmful state of being gathered or focused components "in the hair" of kids with neurodevelopmental disorders like ASD. A survey of field medicine describes demonstrated mercury exposure, whether organic, or inorganic can result in the development of characteristics symptoms that characterize or are frequently observed in autism spectrum disorders (ASD). The (DSM-IV) diagnostic criteria of autism include deficits with interpersonal relationships, having trouble expressing oneself, and engaging in behaviors that are both stereotypical and repetitious , all of which be brought on by mercury.

Comparative biomonitoring of airborne potentially toxic elements using mosses (Hypnum cupressiforme, Brachythecium spp.) and lichen (Evernia prunastri) over remote areas.

The selection of the appropriate biomonitor species is a crucial criterion for biomonitoring on a broad spatial scale. Mosses Hypnum cupressiforme and Brachythecium spp. and lichen Evernia prunastri were sampled at 22 remote sites over Serbia aiming interspecies comparison of their bioconcentration capacities. The concentration of 16 potentially toxic elements (PTEs), Al, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, P, Pb, S, Sr, V, and Zn, was measured in the samples. Between the co-located mosses, linear regression analysis (type II) showed significant determination coefficients only for a couple of the elements (Cd and S), while for H. cupressiforme vs. lichen, significant regression lines were obtained for a broader set of elements (Ba, Cd, Fe, Hg, Mn, Ni, Sr). The ratio of the PTEs in the mosses discovered higher concentrations in H. cupressiforme than in another moss at some sites and vice versa at other sites. According to the PTE ratios, H. cupressiforme accumulated much more element content than the lichen, but followed a similar spatial pattern. In addition, principal component analysis (PCA) pointed out a different grouping of the PTEs depending on the species tested. The poor correlation of the moss-moss data is perhaps because several species of the genus Brachythecium were sampled, which possibly influenced the average genus accumulation capacity. In addition, morphological features of the mosses (concave vs. flat leaflets, creeping vs. cushiony life form) presumably delegate differences in PTE accumulation. To conclude, it should be careful with using more biomonitor species, even of the same genus, within the same study.

Multifunctional antibacterial enhanced amoxicillin carbon nanodots for the detection of Hg (II) and methanol in edible alcohol

Amoxicillin was used as the sole precursor to rapidly synthesize amoxicillin carbon nanodots via a one-step microwave method. The diameter of the amoxicillin carbon nanodots was concentrated at 1.8 ± 0.6 nm, with fluorescence excitation-dependent characteristics. After characterization, the carbon nanodots retained some of the amoxicillin structure, exhibiting low biological toxicity and good antibacterial activity. Due to the formation of the carbon dots structure, the hydrophilicity and water solubility of the amoxicillin carbon nanodots improved. An antibacterial plate experiment further showed that the antibacterial performance of the amoxicillin carbon nanodots was higher than that of the original amoxicillin. The amoxicillin carbon nanodots could quickly and conveniently detect Hg2+ via changes in their fluorescence intensity. Moreover, several aliphatic alcohols could be distinguished and quantified based on the fluorescence intensity increase of the amoxicillin carbon nanodots. Most importantly, the amoxicillin carbon nanodots quickly identified and quantified methanol mixed in edible alcohol. These multifunctional amoxicillin carbon nanodots have broad application prospects in antibiosis, toxic Hg2+ detection, and identification and detection of several aliphatic alcohols, especially the microfluorometric determination of methanol in edible alcoholic beverages.

A new Eosin Y-based ‘turn[sbnd]on’ fluorescent sensor for ratiometric sensing of toxic mercury ion (Hg2+) offering unaided eye detection and its antibacterial activity

A unique fluorescent molecule (ND-S) was obtained from Eosin Y in two simple yet high yielding steps (1). ND-S has special metal ion sensing ability, such that it can selectively detect toxic Hg2+ present in very low concentration in aqueous solutions in the presence of other competing metal ions. The host-guest complexation is ratiometric and is associated with significant increase in fluorescence during the process. Isothermal titration calorimetry (ITC) experiments provided thermodynamic parameters related to interaction between ND-S and Hg2+. Using inductively coupled plasma mass spectrometry (ICP-MS), the Hg2+(aq) removal efficiency of ND-S was estimated to be 99.88%. Appreciable limit of detection (LOD = 7.4 nM) was observed. Other competing ions did not interfere with the sensing of Hg2+ by ND-S. The effects of external stimuli (temperature and pH) were studied. Besides, the complex (ND-M), formed by 1:1 coordination of ND-S and Hg2+ was found to be effective against the survival of Gram-positive bacteria (S. aureus and B. subtilis) with a high selectivity index. Moreover, bacterial cell death mechanism was studied systematically. Overall, we have shown the transformation of a toxic species (Hg2+), extracted from polluted water by a biocompatible sensor (ND-S), into an effective and potent antibacterial agent (ND-M).

CHEMICAL ELEMENTAL COMPOSITION OF DATURA STRAMONIUM L. GROWING IN UZBEKISTAN

Inductively coupled argon plasma mass spectrometry (ICP-MS) was used to study the elemental composition of the underground and aboveground parts of the Datura stramonium growing on the territory of the Republic of Uzbekistan. The obtained data show that 41 elements were found in the composition of the vegetative organs of the D. stramonium, including 6 macroelements (Ca, P, K, Na, S, Mg), 8 essential microelements (Co, Cr, Cu, Fe, Mn, Se, Zn, Mo), and 6 conditionally essential. Moreover, 6 trace elements (B, Si, Ni, V, As, Li), 16 toxic (Pb, Cd, Ge, Sr, Zr, Tl, Bi, Sn, Sb, W, Ag, Ba, Al, Ga, Ti, Be) and 5 little studied elements (Nb, Cs, Ta, Rb, Re) were identified. It was revealed that among the detected elements in D. stramonium, 3 macroelements (Ca, K and Fe) are contained in a concentration of more than 1000 mg/kg, 4 elements (P, S, Mg, Si) are from 100 to 1000 mg/kg, 3 elements (Na, Mn, B), ranging from 10 to 100 mg/kg and the rest were in the range of less than 10 mg/kg. The macroelements were located between each other in the following order: in the roots of the plant Ca (40%)>K (39%)>P (9%)>Mg (6%)>S (4%)>Na (2%), and in the aerial part of the plant Ca (50%)>K (30%)>Mg (9%)>P (7%)>S (3%)>Na (1%). The highest content of essential trace elements in the composition of the roots and aboveground parts of the D. stramonium falls on the share of Fe (n/h 2015.4521 mg/kg, n/h 1516.3041 mg/kg), and among the conditionally essential microelements Si (n/h 397.8607, n/ch 234.4246). It has been established that the higher content of toxic elements in the composition in the underground part of D. stramonium falls on the proportion of A1 (36.92%) and Ti (35.54%), and in the aboveground part of Ga (48.57%) and Al (17.37%), relative to the total content toxic elements. According to the content of salts of heavy metals of the D. stramonium growing in Uzbekistan meets the requirements established by the Global Fund XIV and WHO. Salts of toxic elements Hg were not found. Comparative data showed that in both organs of D. stramonium growing in Uzbekistan, the content of the considered elements is lower than amount of the element of D. stramonium growing in Kazakhstan and South Africa.

Biocompatible Folic-Acid-Strengthened Ag-Ir Quantum Dot Nanozyme for Cell and Plant Root Imaging of Cysteine/Stress and Multichannel Monitoring of Hg2+ and Dopamine.

To boost the enzyme-like activity, biological compatibility, and antiaggregation effect of noble-metal-based nanozymes, folic-acid-strengthened Ag-Ir quantum dots (FA@Ag-Ir QDs) were developed. Not only did FA@Ag-Ir QDs exhibit excellent synergistic-enhancement peroxidase-like activity, high stability, and low toxicity, but they could also promote the lateral root propagation of Arabidopsis thaliana. Especially, ultratrace cysteine or Hg2+ could exclusively strengthen or deteriorate the inherent fluorescence property with an obvious "turn-on" or "turn-off" effect, and dopamine could alter the peroxidase-like activity with a clear hypochromic effect from blue to colorless. Under optimized conditions, FA@Ag-Ir QDs were successfully applied for the turn-on fluorescence imaging of cysteine or the stress response in cells and plant roots, the turn-off fluorescence monitoring of toxic Hg2+, or the visual detection of dopamine in aqueous, beverage, serum, or medical samples with low detection limits and satisfactory recoveries. The selective recognition mechanisms for FA@Ag-Ir QDs toward cysteine, Hg2+, and dopamine were illustrated. This work will offer insights into constructing some efficient nanozyme sensors for multichannel environmental analyses, especially for the prediagnosis of cysteine-related diseases or stress responses in organisms.

Methylmercury Effect and Distribution in Two Extremophile Microalgae Strains Dunaliella salina and Coccomyxa onubensis from Andalusia (Spain).

The main entrance point of highly toxic organic Hg forms, including methylmercury (MeHg), into the aquatic food web is phytoplankton, which is greatly represented by various natural microalgal species. Processes associated with MeHg fate in microalgae cells such as uptake, effects on cells and toxicity, Hg biotransformation, and intracellular stability are detrimental to the process of further biomagnification and, as a consequence, have great importance for human health. The study of MeHg uptake and distribution in cultures of marine halophile Dunaliella salina and freshwater acidophilic alga Coccomyxa onubensis demonstrated that most of the MeHg is imported inside the cell, while cell surface adhesion is insignificant. Almost all MeHg is removed from the culture medium after 72 h. Significant processes in rapid MeHg removal from liquid medium are its abiotic photodegradation and volatilization associated with algal enzymatic activity. The maximum intracellular accumulation for both species was in 80 nM MeHg-exposed cultures after 24 h of exposure for D. salina (from 27 to 34 µg/gDW) and at 48 h for C. onubensis (up to 138 µg/gDW). The different Hg intakes in these two strains could be explained by the lack of a rigid cell wall in D. salina and the higher chemical ability of MeHg to pass through complex cell wall structures in C. onubensis. Electron microscopy studies on the ultrastructure of both strains demonstrated obvious microvacuolization in the form of many very small vacuoles and partial cell membrane disruption in 80 nM MeHg-exposed cultures. Results further showed that Coccomyxa onubensis is a good candidate for MeHg-contaminated water reclamation due to its great robustness at nanomolar concentrations of MeHg coupled with its very high intake and almost complete Hg removal from liquid medium at the MeHg levels tested.

Nitric oxide alleviates mercury toxicity by changing physiological and biochemical pathways in maize (Zea mays L.) seedlings

Like all life forms, plants suffer from high levels of mercury (Hg), known as one of the most harmful heavy metals in soil. The present study was performed to explore the effects of exogenous nitric oxide (NO) on Hg toxicity in maize (Zea mays L., cv. Arifiye-2) seedlings. Plants were grown in a hydroponic system containing 1/2 diluted Hoagland at 16 h day length, 25/20 °C (day/night) and 60% relative humidity. Eight day-old maize seedlings were first treated with NO (as 0.1 µM sodium nitroprusside) and then they were exposed to Hg toxicity (as 100 µM HgCl2) after 24 h. The toxic Hg decreased seedling growth, chlorophyll content, proline content, calcium and manganese contents, non-enzymatic antioxidant contents, cell membrane viscosity, and antioxidant enzyme activities (superoxide dismutase, catalase, peroxidases, and glutathione reductase) while it increased the generation of reactive oxygen species (ROS) such as hydrogen peroxide (H2O2) and super oxide anion (O2.-), and lipid peroxidation (as malondialdehyde, MDA) content and the amount of sodium ion (Na+) in the seedlings. However, NO treatment markedly enhanced the growth parameters (dry and fresh weight, and plant height) and manganese and potassium contents as well as contents of antioxidants and chlorophyll thus alleviating the negative effects caused by the Hg stress. Also, it decreased the generation of ROS and lipid peroxidation level by activating the antioxidant enzymes. These results show that NO in maize seedlings under Hg toxicity may improve stress response and mitigate oxidative stress by stimulating the antioxidant system and modulating ion homeostasis.

Multifunctional Biomass-Based Ionic Liquids/CuCl-Catalyzed CO2-Promoted Hydration of Propargylic Alcohols: A Green Synthesis of α-Hydroxy Ketones.

α-Hydroxy ketones are a class of vital organic skeletons that generally exist in a variety of natural products and high-value chemicals. However, the traditional synthetic route for their production involves toxic Hg salts and corrosive H2SO4 as catalysts, resulting in harsh conditions and the undesired side reaction of Meyer-Schuster rearrangement. In this study, CO2-promoted hydration of propargylic alcohols was achieved for the synthesis of various α-hydroxy ketones. Notably, this process was catalyzed using an environmentally friendly and cost-effective biomass-based ionic liquids/CuCl system, which effectively eliminated the side reaction. The ionic liquids utilized in this system are derived from natural biomass materials, which exhibited recyclability and catalytic activity under 1 bar of CO2 pressure without volatile organic solvents or additives. Evaluation of the green metrics revealed the superiority of this CuCl/ionic liquid system in terms of environmental sustainability. Further mechanistic investigation attributed the excellent performance to the ionic liquid component, which exhibited multifunctionality in activating substrates, CO2 and the Cu component.

Analysis of soil fertility and toxic metal characteristics in open-pit mining areas in northern Shaanxi

The study specifically focused on the Hongliulin mining area, where a total of 40 soil samples were meticulously collected and analyzed from within a 1000 m radius extending from the tailings dam. The findings revealed that soil pH within the 0–1000 m range generally leaned towards the alkaline side. In terms of soil nutrient content, encompassing factors such as soil organic matter (SOM), total nitrogen (TN), total phosphorus (TP), total potassium (TK), alkali nitrogen (AK), available phosphorus (AP), and quick-acting potassium (AK), the variations fell within the following ranges: 2.23–13.58 g/kg, 0.12–0.73 g/kg, 0.18–1.15 g/kg, 9.54–35.82 g/kg, 2.89–6.76 mg/kg, 3.45–11.25 mg/kg, and 5.86–130.9 mg/kg. Collectively, these values indicate relatively low levels of soil nutrients. Within the 0–500 m range of soil samples, the average concentrations of Cd, Hg, Pb, and As were 0.778, 0.198, 24.87, and 17.92 mg/kg, respectively. These concentrations exceeded the established soil background values of Shaanxi Province and emerged as the primary pollutants in the study area. Within this same range, the mean values of eight toxic metals (Pi) were ranked in the following descending order: 1.726 (Hg), 1.400 (As), 1.129 (Cr), 1.109 (Pb), 0.623 (Zn), 0.536 (Cd), 0.309 (Cu), and 0.289 (Ni). With the exception of Hg, As, Cr, and Pb, which exhibited slight pollution, the other toxic metals were found to be within acceptable pollution limits for this sampling range, in line with the results obtained using the geo-accumulation index method. The average potential ecological risk index for the eight toxic metals in the study area stood at 185.0, indicating a moderate overall pollution level. When assessing individual elements, the proportions of ecological risk attributed to Hg, As, Pb, and Cd were 34.57%, 27.44%, 25.11%, and 23.11%, respectively. This suggests that the primary potential ecological risk elements in the study area are Hg and As, followed by Cd and Pb. Notably, toxic metals Hg and Pb, as well as As and Pb, exhibited significant positive correlations within the sampling area, suggesting a common source. An analysis of the relationship between soil physicochemical properties and toxic metals indicated that soil pH, SOM, TN, and TP were closely linked to toxic metal concentrations. The toxic metal elements in the research area's soil exhibit moderate variability (0.16 < CV < 0.36) to high variability (CV > 0.36). Within the range of 0–200 m, the CV values for Cd and Hg exceed 1, indicating a high level of variability. The coefficient of variation for SOM, TP, AP, AK and TK is relatively high with the of 2.93, 2.36, 2.36, 21.01, 7.54. The soil in the sampling area has undergone significant disturbances due to human activities, resulting in toxic metal pollution and nutrient deficiencies.

Metallopeptide-inspired pyridine-bis-tyrosine peptide conjugate mediated facile room temperature synthesis of ultrafine solid mercury nanoparticles for plausible applications

Metallopeptide-inspired, pyridine-bis-tyrosine short peptide conjugate was developed which coordinates Hg(II) ions and hence was further used for the formation of solid mercury nanoparticles at ambient conditions. The formation of solid mercury nanoparticles was obtained from the transformation of stable mercury nanodrops which are guided by peptide nanostructures. Our results showed that initially Hg(II) ions get converted into Hg(0) nanodrops(HgNDs) and stabilized by peptide envelope which subsequently transformed into solid HgNPs with the help of time-dependent electron beam exposure under peptide nanostructure envelope. The solid HgNPs exhibit remarkable rhombohedral morphology and are found crystalline at room temperature. To the best of our knowledge, this is the first report of peptide-mediated electron beam-induced facile synthesis of solid mercury nanoparticles from less toxic Hg(II) ions at room temperature.

Potentially toxic metals in seawater, sediment and seaweeds: bioaccumulation, ecological and human health risk assessment.

This study assesses the bioaccumulation, ecological, and health risks associated with potentially toxic metals (PTMs), including Pb, Hg, Cd, As, and Cr in Hare Island, Thoothukudi. The results revealed that the concentration of PTMs in sediment, seawater, and S. wightii ranged from 0.095 to 2.81mgkg-1, 0.017 to 1.515mgL-1, and 0.076 to 5.713mgkg-1, respectively. The highest concentrations of PTMs were found in the S. wightii compared to seawater and sediment. The high bioaccumulation of Hg and As in S. wightii suggests that it can be used as a bioindicator for these elements in this region. The ecological risk indices, which include individual, complex, biological, and ecological pollution indices, suggest that Hare Island had moderate contamination with Hg and Cd. However, there are no human health risks associated with PTMs. This study examines the current ecological and health risks associated with PTMs and emphasizes the importance of regular monitoring.

Total body burden of neurotoxicant Hg in Chinese mitten crab (Eriocheir sinensis) - Considerations of distribution and human risk assessment

The Chinese mitten crab (Eriocheir sinensis) is considered one of the 100 most invasive alien species in the world. Despite this, its role in ecosystems, among others, in the trophodynamics of pollutants including mercury, is still not fully understood. Becoming an increasingly important and widespread element of the trophic chain in new areas arouses interest from humans as consumers. Hence it is important to determine the level of contaminants (including Hg) in alien species. In the present study, great attention was paid separately to the soft tissues and hard tissues of the exoskeleton, which may play an important role in the detoxification of the crab's body from toxic Hg. The study was conducted on crabs collected in 2011–2021 in the Vistula Lagoon. Concentrations of total mercury and its forms were carried out using a Direct Mercury Analyzer, DMA-80 (Milestone, Italy). The present study showed that mercury accumulation of the crab's body largely occurred through the gills, followed by the oral route. The distribution of Hg in the crab's organs was related to the trophic origin of the mercury, while halide-bound mercury and semilabile forms from the respiration (filtration) process were redistributed into the crab's exoskeleton. Male crabs, compared to females, had a higher Hg burden on internal organs such as their hepatopancreas and gonads. Hg concentration in hard tissues was closely related to the type of mineralization of the carapace. The elimination of Hg from the muscles and from the hepatopancreas into the carapace was one of the important detoxification processes of the crab's body. Thus, moulting crabs effectively remove Hg protecting its body from the neurotoxin. As a result, a smaller Hg load is biomagnified, making the crab's muscle tissue fit for human consumption. The observed decrease in Hg concentrations from 2011 to 2021, as well as the spatial variability of Hg in the crab's muscles, testify that the crab can serve as a biomonitor for ecosystem changes.

A novel triphenylamine based push–pull fluorophore bearing a 2-thiohydantoin unit for toxic Hg2+ ion detection: exploring its potential for live cell imaging

A novel triphenylamine based push–pull fluorophore (TPA-2TH) bearing a 2-thiohydantoin unit for detection of toxic Hg2+ ion and its live cell imaging in Zebrafish.

Rational construction of MoSx via defect engineering for efficient removal of mercury ions from aqueous solution

Mercury ions (Hg2+) are one of the most physiologically toxic heavy metal ions in water. Developing adsorbents for separating and removing mercury ions from aquatic systems has important environmental and social significance. Owing to the hard-soft-acid-base interaction between mercury and sulfur (S) atoms, two-dimensional layered MoS2 holds great promise in capture physiologically toxic Hg2+ from water, but most S atoms are located inside the bulk MoS2, hindering the effective contact with mercury. Defects engineering is considered as an effective way to adjust the structure and achieve superior performance of MoS2. However, reasonable and fine defect modulation to enhance the mercury adsorption performance remains a challenging task. Herein, we reported that molybdenum sulfide with Mo-vacancy structure (MV-MoSx) was fabricated via hydrothermal method and employed to uptake Hg2+. The results showed that this defect type significantly increased the concentration of Mo stripping defects, exposed more active S atoms, and provided MoSx with excellent adsorption performance in adsorption capacity, adsorption kinetics, distribution coefficient, selectivity and so on. In particular, MV-MoSx demonstrates a substantial actual adsorption capacity for mercury, reaching as high as 3723.3 mg/g, which is in close proximity to its theoretical adsorption capacity of 3945.95 mg/g. More importantly, a functionalized composite aerogel system based on MV-MoSx was constructed, which successfully reduced the concentration of Hg2+ solution below the concentration permitted by drinking water standards. Our study not only provide a theoretical basis for the design of novel defect engineering, but also expand the application of transition metal sulfides in the enrichment and separation of heavy metal ions.