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Lead (Pb) is one the 10 chemicals of major public health concern listed by the World Health Organization. One reason for Pb occurrence in food is agricultural practices. In this context, organic production systems are highlighted for not using pesticides, which may result in less chemical contamination in food. Considering that, this systematic review (SR) and meta-analysis was conducted aiming to investigate if there are differences in Pb levels in organic (OLV) and conventional leafy vegetables (CLV). This SR and its protocol (PROSPERO CRD42022306048) were based on PRISMA. Only analytical, cross-sectional studies which reported data on the analysis of Pb in OLV and CLV were included. Searches were conducted in 12 electronic databases besides manual searches in articles, directory, and archives of thesis and dissertations. No restrictions regarding language or publication period were applied. After the selection stages, 24 studies were included, of which 22 (91.67%) presented low risk of bias, while two (8.33%) presented medium risk. Significant difference (p = 0.008) was observed in the meta-analysis considering results in fresh weight (mean difference = 0.01 mg/kg), indicating an inferior concentration of Pb in OLV, being classified as evidence of 'moderate certainty', which answers our research question. [ABSTRACT FROM AUTHOR]

Sharks occupy all living environments of the marine realm as well as some freshwater systems. They display varied and flexible feeding behaviours, but understanding their diet remains challenging due to their elusive ecology and the invasiveness of stomach content analyses in regard of their threatened status. As a potential alternative, we discuss the variability in δ44/42Ca values recorded in the tooth enamel of size‐graded individuals belonging to three species of large sharks with distinct diets (Isurus oxyrinchus, Hexanchus griseus and Carcharodon carcharias). The preliminary results highlight shifts in diet linked to ontogeny (I. oxyrinchus and H. griseus) and spatial distribution (C. carcharias) characterizing feeding behaviour in these species at individual and population level. These outcomes agree with the results of traditional stomach analyses supporting that nontraditional stable isotopes thus represent new perspectives for the study of modern and extinct shark ecology. In addition, for the first time, the Sr/Ca elemental ratios measured in H. griseus reflect sexual differences that could be interpreted in terms of spatial segregation or physiological heterogeneities. [ABSTRACT FROM AUTHOR]

The Arab region is located in an arid environment and suffers from water scarcity and poor water quality which are expected to become more severe in coming years due to global warming. In this study, the groundwater quality of 205 wells in Qatar was investigated. The physical parameters of pH, electrical conductivity (EC), total dissolved solids (TDS), salinity, inorganic carbon (IC), and organic carbon (OC) were determined. The study characterized the concentrations of major anions of Cl, F, Br, NO3, PO4, and SO4, and major cations of Ca, K, Mg, and Na. Importantly, metals and metalloids including V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Ba, Pb, and U were determined. The results revealed that the groundwater of all wells is not drinkable due to high salinity (average TDS 4598 mg/L and salinity 0.4%, respectively). Additionally, average concentrations of major anions Cl, SO4, and F were 1472, 1064, and 1.9 mg/L, respectively, and all exceed the World Health Organization (WHO) guidelines for drinking water. However, NO3 concentration in 11 out of 205 wells was above the WHO guidelines of 50 mg/L due to intensive agriculture and fertilizer applications. Major cations of Ca, K, Mg, and Na were higher than WHO guidelines with average concentrations of 345, 63, 127, and 923 mg/L, respectively. All trace metals were much lower than the WHO guidelines for drinking water; however, the vanadium (V) average concentration in groundwater of all wells was 31 μg/L, which is five times higher than the Dutch guidelines (whereas the WHO has no guidelines for V). The groundwater of Qatar is dominated by Ca and Mg sulfates in Sabkha environments and dominated by NaCl in the coastal zones from evaporate environments consisting of coastal salt flats, salt pans, estuaries, and lagoons supersaturated by salts and the influence of sea water intrusion. [ABSTRACT FROM AUTHOR]

For proper functioning of the human body, several metals are required in different concentrations but if their concentration slightly elevates, because of any metal-contaminated environment or of other food sources, which leads to high toxicity and different chronic health issues. Different analytical techniques like atomic absorption spectroscopy, X-ray fluorescence, inductively coupled plasma- mass spectroscopy (ICP-MS) and flame atomic absorption spectroscopy are used for metals analysis present in different samples in different fields but nowadays neutron activation analysis (NAA) is preferred over other analytical techniques because it is an efficient, multi-elemental, nondestructive analytical technique having an ultralow minimum detection limit, therefore it can detect heavy metals (HMs) even if at a very trace level parts per billion (ppb) with a quite simple sample preparation technique. This technique is known as "referee technique" because of its accuracy and trustworthiness. There is a widespread use of this technique in biomedical science like in Alzheimer's disease, cancer, arthritis, metabolism study, brain tumor and in many more conditions where metals are actively present. For its typical sample sizes and due to a multitude of additional benefits, it also helps in mapping of pathophysiology of the disease. Besides all, mainly in biomedical science the biological samples can easily be analyzed irrespective of any form. In recent years NAA is preferred over other analytical techniques in several research fields, so this article focuses on the analytical technique, its general principle and recent applications. [ABSTRACT FROM AUTHOR]

Lead (Pb) is a non-essential and toxic metal for plants. Current study was planned to assess Pb-induced toxicity with and without NaCl in a halophyte Arthrocaulon macrostachyum. Three month old seedlings (after germination) were grown in pots containing quartz sand and sub-irrigated with 300 mM NaCl and different Pb(NO 3) 2 concentrations (0, 0.75, 3, 6 and 12 mM) in plastic trays where 0 mM NaCl and Pb(NO 3) 2 were taken as control for monitoring growth, physiological and biochemical characteristics. Plant growth (height and biomass) was optimized in 300 mM NaCl while progressive increases in fresh weights up to 3 mM Pb(NO 3) 2 may be related to better shoot turgor, succulence and more plant pigments. Growth was substantially reduced in 6 and 12 mM Pb(NO 3) 2 both with and without NaCl. Plant shoots accumulated higher levels of Pb and Na+ of up to 3 mM Pb;while root Pb increased in > 6 mM Pb(NO 3) 2 treatments. Decreased pigments, potential quantum yield (F v /F m) and yield of photosystem II (ɸ PSII) enhanced the accumulation of H 2 O 2 , electrolyte leakage and consequently reactive oxygen species (ROS) in 12 mM Pb(NO 3) 2. The scavenging of ROS was manifested with the increased in vitro activity of superoxide dismutase (SOD) of up to 6 mM Pb(NO 3) 2 ; whereas higher Guaiacol peroxidase (GPx) may be related to cell wall hardening and poor growth. The increases in SOD, marginal changes in catalase (CAT) and unchanged APX of up to 6 mM Pb(NO 3) 2 demonstrated the activation of stress-responsive metabolism in Arthrocaulon machrostachyum ; and Pb accumulation of up to 200 mg kg-1 making this species a useful candidate for Pb phytoremediation. [Display omitted] • Arthrocaulon macrostachyum plants were able to tolerate up to 6 mM while 12 mM Pb (NO 3) 2 concentration was highly inhibitory to growth. • Arthrocaulon macrostachyum plants accumulated up to 200 mg kg−1 Pb under saline conditions. • The dual stress tolerance to Pb and salts in Arthrocaulon macrostachyum was associated with optimised regulation of water balances, ion fluxes and antioxidant feedback. [ABSTRACT FROM AUTHOR]

The presence of residual antibiotics and the excessive accumulation of metals beyond permissible limits in milk represent significant health challenges. This study aimed to analyse the levels of heavy metals and trace elements in raw milk from Kurdistan province using inductively coupled plasma mass spectrometry (ICP‐MS) following digestion via thermal block. Subsequently, the samples were evaluated for contamination with MRSA (methicillin‐resistant Staphylococcus aureus), taking into account the potential correlation between methicillin‐resistant strains and metal accumulation. Finally, milk safety was assessed based on the presence of toxic metals. A total of 180 milk samples were examined. Among them, 13.34% were found to be contaminated with S. aureus, and of those, 62.48% tested positive for MRSA. The metal concentrations (mg/kg) were measured as follows: arsenic 7 × 10−2 ± 6 × 10−3, cadmium 4.70 × 10−1 ± 9.70 × 10−2, lead 7 × 10−2 ± 5 × 10−3, mercury 3 × 10−2 ± 9 × 10−3 and iron 4 × 10−2 ± 9 × 10−3. Interestingly, arsenic, cadmium and iron levels were found to be correlated with the presence of MRSA. Additionally, there was an inverse relationship between toxic metals and essential ones in samples sensitive to methicillin (P < 0.001). The Target Hazard Quotient (THQ) for cadmium is indicated at 9.94. Furthermore, the calculated Carcinogenic Risk (CR) parameters for cadmium and arsenic were 6.06 × 10−3 and 2.22 × 10−4, respectively, suggesting that their concentrations fall within the carcinogenic range. The coexistence of MRSA and metal contamination in raw milk highlights the potential risks linked to its consumption. Consequently, the adoption of rigorous hygiene protocols is imperative to effectively address these concerns. [ABSTRACT FROM AUTHOR]

Serpentine ecosystems are characterised by multiple environmental stressors: high levels of trace metals such as nickel (Ni), low availability of macronutrients and low water retention. These harsh environmental conditions exert a strong selective force on the vegetation, but their effect on community assembly processes and the functional trait composition remains unknown. In 26 plots on four serpentine sites on Lesbos Island (Greece), we measured six leaf functional traits related to resource acquisition and stress resistance on the 20 most abundant plant species. We quantified the proportion of variance explained by inter‐ and intraspecific trait differences and tested if individual species showed changes in trait values explained by soil Ni content. We investigated the adaptive value and the community level changes for each trait along the natural soil Ni gradient using a mixed model approach and functional diversity analyses. We tested the role of the abundant serpentine endemic and Ni‐hyperaccumulating species Odontarrhena lesbiaca in driving these patterns. Intraspecific variation explained by soil Ni content is smaller than 4%, and most of the variance is explained by interspecific differences in trait values. Most species do not show significant changes in trait values in response to soil Ni. At the community level, low specific leaf areas, small and thick leaves are selected on high Ni soils. Functional diversity analyses suggest a shift towards a stress tolerance syndrome (thick and small leaves with low SLA values) and an increase in functional diversity on Ni‐rich soils. However, these patterns are driven by the increasing abundance of O. lesbiaca. The endemic Ni hyperaccumulator has a stress tolerance strategy with small thick leaves and low SLA, while the community of broadly distributed species show an increase in trait values related to dominance and fast growth. Synthesis. Intraspecific variation in leaf trait responds little to soil metal toxicity. Endemic species harbour unique trait values compared to species with broad distribution which should justify their conservation as a priority. [ABSTRACT FROM AUTHOR]

Granite-related W-Sn ore systems are commonly associated with coeval Pb-Zn mineralization. It remains unclear whether these metals are derived from the same sources or not. Mercury (Hg) is a common minor component in such systems. Hg isotopes undergo unique mass-independent fractionation (expressed as Δ199Hg values), which is mainly generated during Hg photochemical reactions on Earth's surface and not affected by magmatic-hydrothermal processes, offering an excellent opportunity to trace metal sources in hydrothermal systems. We observed near-zero Δ199Hg values in wolframite (−0.10‰ to 0.08‰, n=11), and in skarn- (−0.17‰ to 0.12‰, n=48) and greisen-type (−0.12‰ to 0.10‰, n=11) bulk tin-tungsten ore from eight major ore deposits in South China. These values are identical to those of coeval highly evolved granites (−0.13‰ to 0.12‰, n=49), supporting that Hg in W-Sn ores were sourced from granite. However, sulfides (e.g., pyrite, chalcopyrite, arsenopyrite, galena, and sphalerite) in these deposits exhibit negative to near-zero Δ199Hg values (−0.42‰ to 0.09‰, n=124), which indicates a contribution of Hg and by inference other metals from both Precambrian basement rocks (Δ199Hg<0) and ore-related granites. The study demonstrates that multiple sources of metals were involved in the formation of the polymetallic W-Sn deposits, and further highlights that extraction of metals from basement rocks may be a critical control on the formation of economically important mineralization of base metal sulfides (e.g., Pb, Zn) in granite-related magmatic-hydrothermal systems. [ABSTRACT FROM AUTHOR]

BACKGROUND: The large amounts of iodine in brown seaweeds may contribute towards an adequate iodine intake, but also pose a food safety risk. In the current work we estimate the maximum amount of the cultivated brown seaweeds Saccharina latissima and Alaria esculenta (blanched and non‐blanched) that can be added to white loaf‐type wheat‐bread so European consumers are protected against excessive chronic intakes. We use data for high‐level consumers of bread with special ingredients added from the EFSA comprehensive European food consumption database to construct a conservative risk management model. We bake prototype seaweed bread and use the output from the model to assess exposure to iodine and trace metals. We also assess some bread quality parameters such as sensory characteristics, crumb firmness and specific volume. RESULTS: The maximum level of iodine in bread that would mitigate the European consumer from excess intakes was 857 μg I kg−1 bread. Assuming a typical 60% wheat flour per kilogram of bread, a maximum amount of 11.3 g of dried blanched A. esculenta (115 mg I kg−1 dry weight) could be incorporated per kilogram of wheat flour into the bread recipe whilst for non‐blanched S. latissima, which contained 3500 mg I kg−1 dry weight, only a minuscule 350 mg of seaweed was the limit. For prototype breads, seaweed addition had no significant impact on the specific volume and crumb firmness. Levels of cadmium and arsenic in the bread were also of low toxicological concern. CONCLUSION: A maximum 1–2% brown seaweed of total flour weight could be added to bread to contribute towards European consumers' adequate iodine intake without overexposure. © 2024 The Author(s). Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

The international GEOTRACES program has been instrumental in demonstrating how marine sediments are a critical source of dissolved Fe to the world's oceans. Here, we present dissolved iron (dFe) from the GEOTRACES North Pacific GP15 section, which, alongside other sediment‐source tracers (including dissolved δ56Fe, Mn, 228Ra, and particulate Fe), allows for identification of the dFe provenance of three distinct dFe depth maxima at the Alaskan margin. Two of these (shelf and abyssal depths) are of local Alaskan sedimentary origin. The third, a mid‐depth dFe maximum with an absence of 228Ra, is an advected signal that, based on tracer data from Western Pacific GEOTRACES transects and circulation models, must be advected from sedimentary sources on the Asian margin, ∼5,000 km away. This study illustrates the importance of measuring diagnostic sedimentary tracers like radium when assigning local margins as sedimentary sources of marine trace metal budgets. Plain Language Summary: Iron is an essential, yet limiting, micronutrient for marine primary producers, and thus influences patterns of global oceanic primary productivity and carbon exchange. In recent years, the International GEOTRACES program has highlighted that marine sediments, hydrothermal vents, and atmospheric dust all supply dissolved iron to the oceans. Here, we investigated the sources of dissolved iron to the Eastern North Pacific Ocean, using samples collected on the U.S. GEOTRACES GP15 Pacific Meridional Cruise that sailed from Alaska to Tahiti in 2018. We identified three elevated dissolved iron features close to the Alaskan continental margin, with two originating from local sedimentary sources (shelf and abyss). The third, an intermediate depth dissolved iron plume that extends south into the gyre, is not of local sedimentary origin, but instead results from long‐distance transport of dissolved iron from Asian marginal sediment sources. A critical aspect of this study is the use of multiple chemical tracers such as radium, iron, and manganese, coupled with ocean circulation models, to correctly attribute the sources of trace metals to the ocean. Key Points: Three distinct dFe maxima were identified close to the Alaskan margin at different depths. Two are of local origin (shelf and abyssal)An intermediate depth dFe plume with an absence of Mn and Ra, is a distal advected signal from Asian margin sedimentary sources (5,000 km away)A multiple tracer approach of Fe, Mn, and Ra was necessary to rule out what appeared to be a local margin source [ABSTRACT FROM AUTHOR]

Heavy metal contamination is a serious global issue that threatens both environmental and human health. This study investigated the levels of 12 heavy metals in sediments, roots, stems, and leaves of Phragmites australis (common reed) from a river in Iran, using an inductively coupled plasma optical emission spectrometer (ICP-OES). The sediment metal concentration order was: Aluminum (Al) > Iron (Fe) > Manganese (Mn) > Zinc (Zn) > Magnesium (Mg) > Nickel (Ni) > Chromium (Cr) > Lead (Pb) > Copper (Cu) > Arsenic (As) > Vanadium (V) with Cadmium (Cd) below detection limit. Concentrations of As, Ni, Pb, and Zn in the sediments exceeded background values. According to sediment quality guidelines (SQGs), metal concentrations were between the threshold effect level (TEL) and the probable effect level (PEL), remaining below the severe effect level (SEL), except for Ni. Average metal concentrations in plant tissues were lower than in sediment samples, with roots showing higher levels of Cd, V, Cu, Pb, Zn, As, Al, Mg, and Fe than in the shoots, while leaves had higher Ni, Cr, and Mn. The bioaccumulation factor of less than 1 (except for V) indicates limited bioavailibility of these metals. [ABSTRACT FROM AUTHOR]

Vermiculite is extensively utilized for several applications, including as a hydroponic substrate, for soil conditioning, oil cleansing, and addressing trace metal pollution. In this study, the expansion of natural vermiculite was easily achieved by utilizing hydrogen peroxide (H2O2) with the aid of microwave technology. The characterization of expanded vermiculite involved the use of X‐ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), nitrogen adsorption isotherm (BET), and energy dissipation X‐rays (EDX). The vermiculite has been enlarged to have a structure resembling flakes, and its surface area measures 73.9 m2/g. The adsorption of Alizarin Red S onto expanded vermiculite was investigated under varying conditions, such as pH, starting concentration, adsorbent content, and duration of exposure. The enlarged vermiculite achieved a maximum adsorption capacity of 182.5 mg/g for Alizarin Red S. Out of the three adsorption isotherm models, both the Freundlich and Temkin models accurately describe the adsorption of Alizarin Red S onto expanded vermiculite. When studying adsorption kinetics, the second‐order adsorption kinetic model is more appropriate than the first‐order adsorption kinetic model, as indicated by an R2 value of 0.8964. [ABSTRACT FROM AUTHOR]

This study was designed to evaluate the health risks faced by inhabitants living in the slum areas of Addis Ababa, Ethiopia. The levels of PM2.5 and PM10 and elemental composition of the PM10 were measured in indoors (in the kitchen and living room) and outdoors (at the roadside). A total of 75 sampling locations (45 indoor and 30 outdoor) were selected for the study. The levels of PM2.5 and PM10 were determined using an AROCET531S instrument, while an universal air pump was used for the sampling of PM10 for the determination of trace elements by inductively coupled plasma-optical emission spectroscopy (ICP‒OES). The health impacts of PMs on the inhabitants of twelve microenvironments (MEs), where they spend much of their daily time, were estimated. The total amounts of PM2.5 and PM10, and trace metals in PM10 found in the nine or twelve MEs ranged from 10.6–119, 128–185, and 0.007–0.197 μg m-3, respectively. According to the United States Environment Protection Agency (USEPA) guidelines, ten of the twelve MEs can cause significant health problems for inhabitants (HI > 1) due to PM2.5 and PM10. Thus, special attention should be given by stakeholders/inhabitants to minimize the health impacts on long-term exposure. This study assessed the risk of levels of trace elements on the inhabitants who spend most of their daily lives. The study revealed that the lifetime cancer risk values for the individual and cumulative trace elements were within the tolerable range set by the USEPA guidelines. [ABSTRACT FROM AUTHOR]

Aim Methods Results Conclusion Composts made from food waste will soon become more widespread on the market thanks to the upcoming enforcement of the legal obligation to sort biowaste. Our experiment aims at improving knowledge on the short‐term effects of these composts on soils’ physicochemical properties and vegetable crops.Three composts with contrasting characteristics were tested: a 100% v/v green waste compost (C1), and two composts composed of 50% v/v food waste and 50% v/v green waste, one prepared directly on the soil (C2) and the other from a competing producer who have the French NFU 44‐051 (AFNOR NF U 44‐051, 2006) certification for an organic amendment (C3). They were applied at a rate of 100 t ha−1 (dry matter) on two cropped soils with contrasting textures. Soil‐and‐compost mixes and compost‐free soil were planted with lettuce, radish, and potato.Seventy‐four days after planting, composts improved some soil physicochemical properties. The compost‐amended soils had better saturated hydraulic conductivity (Ks, 1 10−3–2.5 10−3 cm s−1) than the compost‐free soil (0.5 10−3 cm s−1), and water‐stable aggregates were higher than the initial value in C3 soil, equal to it in C2 soil, and lower in C1 soil. pH, total nitrogen, and organic carbon increased in all compost‐amended soils. Food waste compost stimulated crop production. The yields (dry matter) of all three crops were two to three times higher in the two soils amended with food waste compost compared to unamended soil, whereas they decreased almost two times in the soil amended with green waste compost due to nitrogen immobilization. Trace metals (particularly Pb and Cd) added by the composts, although present in edible parts of the plants, did not exceed the European rules for trace metals.Thus, food waste composts have positive effects on soils and vegetable crops, and the higher their organic matter content, the higher these positive effects. [ABSTRACT FROM AUTHOR]

The excessive accumulation of heavy metals has adverse effects on the human body. Here, magnetic iron oxide‐impregnated carboxymethyl‐β‐cyclodextrin was synthesized. The synthesized material was employed as a magnetic solid‐phase extracting adsorbent for specific heavy metals like lead (Pb), nickel (Ni), copper (Cu), and cobalt (Co). Characterization was performed by X‐ray diffraction, energy dispersive X‐ray spectroscopy, scanning electron microscopy, Brunauer–Emmett–Teller, and Fourier‐transform infrared spectroscopy. The analytical merits, like detection limits (Pb: 1.38 ng/mL, Ni: 0.5 ng/mL, Co: 0.14 ng/mL, and Cu: 0.55 ng/mL) and quantification limits (Pb: 4.14 ng/mL, Ni: 1.62 ng/mL, Co: 1.85 ng/mL, and Cu: 1.82 ng/mL) were calculated. Similarly, the preconcentration and enhancement factors (15) and relative standard deviation (Pb: 3.5, Ni: 0.92, Co: 2.7, and Cu: 1.5) were also calculated. The interfering study shows that the method is highly selective. For validation, it was applied to certified reference materials such as the Institute of Nuclear Chemistry and Technology ornamental Basma tobacco leaves and trace metal double addition 63.4 environmental water with good percent recovery values (92%–99%). Real water and food samples were also used with satisfactory (90%–99%) recovery results. [ABSTRACT FROM AUTHOR]

Understanding fish movement in river systems is essential in identifying habitats which are important for species to perpetuate. Water chemistry, paired with fish otoliths, can be used to trace movements among different habitats, although a detailed understanding of spatial variation in water chemistry is first required. To obtain this knowledge, we analysed surface water collected from 59 sites throughout the Clarence River Basin, a coastal river basin in northern New South Wales, Australia. The primary objective was to quantify the spatial variation of trace metals and strontium isotope ratios (87Sr:86Sr) for future and paired use with otolith microchemistry to track fish movement. Using ICP-OES, we identified that some trace metals, particularly strontium and barium as well as 87Sr:86Sr ratios, varied spatially when analysing all water samples and revealed three distinct regions centring around the estuary, interior and outer regions. These differences were driven by variation in the underlying surface geology between the Clarence–Moreton Basin and the New England Block. Tidal influence also affected trace metals and 87Sr:86Sr ratios throughout the estuarine area. We suggest that the level of differentiation identified in the current study has the potential to discriminate broad-scale fish movements among regions/habitats using otolith analysis, with fine scale movements best elucidated using complementary techniques. [ABSTRACT FROM AUTHOR]

Considering the urgency of resource utilization and environmental protection, the geochemistry of anomalous trace transition metal elements in coal formed in terrestrial environments has been studied using methods such as inductively coupled plasma atomic emission spectrometry analysis, electron probe micro-area analysis, sequential chemical extraction procedures, and correlation analysis. The results indicate that minerals in the coal samples included pyrite, kaolinite, quartz, dolomite, calcite, and celestite. Furthermore, compared with the average values of coals in China and the upper continental crust, the coal samples were rich in transition metal trace elements such as Ni, Cr, and Sr and were deficient in Be, Cd, Cu, Co, Ga, Mo, Sb, Tl, V, Zn, and Ti. We found that Ni preferentially occurred in the organic matter over minerals, while Cr primarily bonded with sulfide minerals and to a lesser extent with the iron-manganese oxide minerals. Sr had a low correlation with organic matter but adhered to clay minerals and celestite. Ni enrichment in coal samples was the result of terrigenous input, while the Cr enrichment was related to intrusion of magmatic hydrothermal fluids. Sr enrichment was caused by the presence of SO42- in the terrigenous debris and the influence of Sr-rich water underground. [ABSTRACT FROM AUTHOR]

The aim of this study is to evaluate the lubricating performance of various base oils in a hydrogen-enriched environment. Experiments were conducted wherein base oils were emulsified with meticulously calibrated hydrogen concentrations, followed by a series of friction and wear measurements. Elemental analysis was performed on the worn surfaces, providing further insight into the wear mechanism. The findings of this study highlight the pronounced effect of hydrogen on the lubrication of pure water emulsions of Class IV 4 base oils, with the Class V 5-1 base oils showing optimal lubricating performance in hydrogen-enriched conditions. SEM images at high magnification scanning revealed the presence of a protective friction film on the surfaces of the wear scars in each sample. X-ray photoelectron spectroscopy (XPS) identified traces of metal sulfide within the friction film, which may play a role in reducing friction. The formation of this friction film is likely a contributing factor to the enhanced lubricating performance of the base oil. These findings contribute a substantial foundation for the development of standards for evaluating the performance of hydrogen internal combustion engine oils. [Display omitted] • Study on water emulsification of oil in hydrogen internal combustion engine. • The participation of hydrogen plays an anti-wear and anti-friction effect. • The lubrication effect of hydrogen on class IV emulsion is significantly improved. • The lubrication effect of class V emulsion is the best in hydrogen environment. • The participation of hydrogen contributes to the formation of metal sulfide films. [ABSTRACT FROM AUTHOR]

This study aimed to observe changes in the diet of crab Eriphia gonagra due to the oil spill that occurred in 2019 on two beaches on the Pernambuco coast (Gaibu and Carneiros Beach) Northeastern, Brazil. Changes in the species feeding were investigated considering the periods before, during, and after of the spill and correlated with the analysis of sediment contamination Polycyclic Aromatic Hydrocarbons (PAHs) and Trace Metals (TM). 160 specimens were analysed. 24 food items were found, with a prevalence of Mollusca (fragment) and Macroalgae in the diet. There was no detection of oil fragments in the stomachs of animals, however, different patterns were observed in the feeding of the species studied in the BEF, DUR, and AFT periods of the spill. A generalist habit, it was possible to observe changes in captured items, thus we observed a diet with low nutritional levels caused mainly in impacted environments. Two factors may be prevalent in explaining the impacts caused by the feeding of E. gonagra in Carneiros Beach. The first was the decrease in prey that died after the arrival of the oil, the second was the lasting effects of contaminants on the predation capacity of the species. [ABSTRACT FROM AUTHOR]

Mercury, a trace metal, is a persistent environmental pollutant that can be detected even in remote regions, including high-mountain lakes. This study examined mercury concentrations in the sediment of two lakes in the French Pyrenees, the Legunabens and Labant lakes. Sediment samples were collected using a Hon-Kajak Sediment Corer, and mercury concentrations were measured following the EPA 7473 method with a direct mercury analyzer (DMA-80). Mercury levels reached up to 283 ng g−1 in the Legunabens lake and up to 110 ng g−1 in the Labant lake, possibly linked to the mining history of the Ariège department and atmospheric deposition from distant sources. These findings indicate significant contamination, ranging from an 8% to 42% probability of generating adverse biological effects according to Canadian standards, and approximately 90% higher concentrations compared to average mercury concentrations in other Pyrenean lakes. Such contamination poses potential risks to aquatic life and the environment due to mercury's toxicity and bioaccumulation in microorganisms. [ABSTRACT FROM AUTHOR]

Copper is an essential micronutrient and the ability to scavenge tightly bound or trace levels of copper ions at the host–pathogen interface is vital for fungal proliferation in animal hosts. Recent studies suggest that trace metal ion acquisition is critical for the establishment and propagation of Pseudogymnoascus destructans, the fungal pathogen responsible for white-nose syndrome (WNS), on their bat host. However, little is known about these metal acquisition pathways in P. destructans. In this study, we report the characterization of the P. destructans high-affinity copper transporter VC83_00191 (PdCTR1a), which is implicated as a virulence factor associated with the WNS disease state. Using Saccharomyces cerevisiae as a recombinant expression host, we find that PdCTR1a can efficiently traffic Cu ions into the yeast cytoplasm. Complementary studies in the native P. destructans fungus provide evidence that PdCTR1a transcripts and protein levels are dictated by Cu-bioavailability in the growth media. Our study demonstrates that PdCTR1a is a functional high-affinity copper transporter and is relevant to Cu homeostasis pathways in P. destructans. [ABSTRACT FROM AUTHOR]

Air pollution is the most important environmental problem in urban areas related to vehicular traffic and industrial activities. The widespread presence of common urban trees, such as Salix humboldtiana, and their ability to tolerate diverse environmental conditions make this species an especially promising candidate for assessing environmental metal contamination. Therefore, biomonitoring with vascular plants has been widely used to assess air pollution, especially the accumulation of trace metal concentrations. Therefore, for the first time, we analyzed the concentration of trace metals using Salix humboldtiana in twelve areas with different levels of pollution in a city in Southern Ecuador. For this purpose, samples were taken from each site to assess the accumulation of trace metals such as Zn, Mn, Fe, Cd, Cr, Pb, Cu, Al, and Ni. The results obtained showed significant differences in the concentrations of Zn, Mn, Fe, and Cd between the urban areas and the control area, indicating that the central areas were the most polluted by vehicular traffic. However, these findings suggest that Salix humboldtiana may not be a particularly effective tool for quantifying levels of environmental metal contamination such as Cu and Ni, at least in urban areas in the city of Loja. This study has demonstrated that Salix humboldtiana leaves can effectively monitor trace metals associated with road traffic emissions in areas with varying levels of vehicular activity, indicating that vascular plants can be utilized for this purpose in tropical cities. [ABSTRACT FROM AUTHOR]

Trace metals are required as cofactors in metalloproteins that are essential in microbial metabolism and growth. The microbial requirements of diverse metals and the capabilities of prokaryotic taxa to acquire these metals remain poorly understood. We present here results from metagenomic observations over an entire productive season in the region off Kerguelen Island (Indian Sector of the Southern Ocean). We observed seasonal patterns in the abundance of prokaryotic transporters of seven trace elements (zinc [Zn], manganese [Mn], nickel [Ni], molybdenum [Mo], tungsten [W], copper [Cu] and cobalt [Co]) and the consecutive spring and summer phytoplankton blooms were strong drivers of these temporal trends. Taxonomic affiliation of the functional genes revealed that Rhodobacteraceae had a broad repertoire of trace metal transporters (Mn, Zn, Ni, W and Mo) and a more restricted set was observed for other prokaryotic groups, such as Flavobacteriaceae (Zn), Nitrincolaceae (Ni and W) and Thioglobaceae (Mo). The prevalence of trace metal transporters within a prokaryotic group, as determined on the family level, was overall confirmed in representative metagenome‐assembled genomes. We discuss the potential involvement of prokaryotic groups in processes related to organic matter utilisation that require these metals and the consequences on carbon and trace metal cycling in surface waters of the Southern Ocean. [ABSTRACT FROM AUTHOR]

Background: The pathogenesis of Crohn's disease involves genetic and environmental factors, with the gut microbiome playing a crucial role. The Crohn's disease-associated variant rs13107325 in the SLC39A8 gene results in an A391T substitution in the ZIP8 metal ion transporter and has previously been linked to alterations in the colonic microbiome in variant carriers. We hypothesized that the A391T substitution alters metal ion homeostasis in the colonic mucosal–luminal interface, thereby inducing dysbiosis which may promote intestinal inflammation. Methods: To evaluate this hypothesis, we generated a SLC39A8 A393T mouse model (matching human A391T). We first examined trace element abundance in the colonic mucosal epithelium and lumen of homozygous A393T and wild-type (WT) mice to determine if the variant affected metal distribution. We also performed 16S rRNA gene sequencing on colon samples at 2 months, 3–4 months, and 12 months of age, and conducted histological scoring of colon tissue collected from 5-month and 10-month old mice. Results: Consistent with an effect of the variant on ZIP8 function, homozygous A393T mice exhibited increased cobalt in the colonic mucosa, but reduced iron, zinc, manganese, cobalt, copper, and cadmium in the colonic lumen. 16S rRNA gene sequencing of colon samples revealed variant-linked effects on microbiome beta diversity in 2-month-, 3–4-month-, and 12-month-old mice. Histological scoring showed spontaneous intestinal inflammation in 10-month but not in 5-month-old mice. Lastly, predicted pathway analysis of the microbiome samples revealed differential enrichment of iron-, zinc-, and cobalt-dependent pathways in A393T mice compared to wild-type controls. Conclusion: These results suggest that the variant in SLC39A8 primarily restricts metal availability to the microbiota, resulting in compositions that can adapt to the environment and that A393T-linked dysbiosis occurs prior to the onset of inflammation. This study paves the way for future studies investigating risk variants as microbiome-disease modifiers. [ABSTRACT FROM AUTHOR]

In fish, the gill plays a vital role in regulating the absorption of trace metals and is also highly susceptible to metal toxicity. Trace metals such as iron (Fe), copper (Cu), zinc (Zn), and manganese (Mn) are involved in various catalytic activities and molecular binding within the gill, thereby supporting a range of physiological processes in this organ. While beneficial at normal levels, these metals can become toxic when present in excess. Conversely, nonessential metals like cadmium (Cd) and lead (Pb) can gain entry into gill cells through similar metal transport pathways, potentially interfering with various cellular processes. The transepithelial transport of these metals across the gill epithelium is governed by a variety of metal transport and metal binding proteins. These include the Cu transporter 1 (CTR1), divalent metal transporter 1 (DMT1), and members of the Zrt-/Irt-like protein (ZIP) and zinc transport (ZnT) families. Additionally, some of these metals can compete with major ions (e.g., calcium, sodium) for absorption sites in the gill. This complex crosstalk suggests an interdependent mechanism that balances metal uptake to meet physiological needs while preventing excessive accumulation. In this article, I review the roles of trace metals in proteins/enzymes that support the different functions in the gill of teleost fish. I also discuss current understanding of the pathways involved in regulating the branchial uptake of metals and their influence on ionic regulation, and the potential detoxification mechanisms in the gill. Finally, I summarize knowledge gaps and potential areas for further investigation. [ABSTRACT FROM AUTHOR]

Digital light processing (DLP) 3DP, commercial acrylate-based photocurable resins, and thermally expandable microspheres-incorporated flexible photocurable resins were employed to fabricate an SPE column with a thermally expanded monolithic foam for extracting Mn, Co, Ni, Cu, Zn, Cd, and Pb ions prior to the determination using inductively coupled plasma mass spectrometry. After optimization of the thermally activated foaming, the design and fabrication of the SPE column, and the automatic analytical system, the DLP 3D-printed SPE column with the thermally expanded monolithic foam extracted the metal ions with up to 14.8-fold enhancement (relative to that without incorporating the microspheres), with absolute extraction efficiencies all higher than 95.6%, and method detection limits in the range from 0.5 to 5.2 ng L–1. We validated the reliability and applicability of this method by determination of the metal ions in several reference materials (CASS-4, SLRS-5, 1643f, and Seronorm Trace Elements Urine L-2) and spiked seawater, river water, ground water, and human urine samples. The results illustrated that to incorporate the thermally expandable microspheres into the photocurable resins with a post-printing heating treatment enabled the DLP 3D-printed thermally expanded monolithic foam to substantially improve the extraction of the metal ions, thereby extending the applicability of SPE devices fabricated by vat photopolymerization 3DP techniques. [ABSTRACT FROM AUTHOR]

Over the years, prostate cancer (PCa) research has been of great interest, and trace metals have attracted a lot of attention due to their association with prostate cancer development and progression. PCa has a complex etiology, with genetic, environmental, and lifestyle factors being implicated. Trace metals such as zinc (Zn), mercury (Hg), selenium (Se), lead (Pb), cadmium (Cd), manganese (Mn), arsenic (As), and nickel (Ni) have garnered much attention in recent years, suspected of having direct links to the modulation of cancer risk and progression through their impacts on prostate cancer omics (genomics, epigenetics, proteomics, and transcriptomics). This has led to them being the subject of extensive research in this regard. In this review, we explored the influence of trace metals and offered a comprehensive analysis of the current knowledge on how trace metals affect the biology of prostate cancer at a molecular level by integrating findings from the recent literature to help suggest possible directions for future research. [ABSTRACT FROM AUTHOR]

Copper is a vital trace element in oxidized and reduced forms. It plays crucial roles in numerous biological events such as redox chemistry, enzymatic reactions, mitochondrial respiration, iron metabolism, autophagy, and immune modulation. Maintaining the balance of copper in the body is essential because its deficiency and excess can be harmful. Abnormal copper metabolism has a two-fold impact on the development of tumors and cancer treatment. Cuproptosis is a form of cell death that occurs when there is excessive copper in the body, leading to proteotoxic stress and the activation of a specific pathway in the mitochondria. Research has been conducted on the advantageous role of copper ionophores and chelators in cancer management. This review presents recent progress in understanding copper metabolism, cuproptosis, and the molecular mechanisms involved in using copper for targeted therapy in cervical cancer. Integrating trace metals and minerals into nanoparticulate systems is a promising approach for controlling invasive tumors. Therefore, we have also included a concise overview of copper nanoformulations targeting cervical cancer cells. This review offers comprehensive insights into the correlation between cuproptosis-related genes and immune infiltration, as well as the prognosis of cervical cancer. These findings can be valuable for developing advanced clinical tools to enhance the detection and treatment of cervical cancer. [ABSTRACT FROM AUTHOR]

A novel method was developed for the rapid detection of heavy metals in firework solutions with high sensitivity and minimal pretreatment by enriching them with ethylenediaminetetraacetic acid (EDTA) reagent and analyzing them using microwave plasma torch mass spectrometry (MPT‐MS). Quantitative results showed that the limits of detection and quantification for heavy metals (Pb, Ba, Sr, and Ag) ranged from 0.05 to 0.25 and 0.38 to 0.71 μg·L−1, respectively. The linear dynamic ranges covered at least two orders of magnitude, with correlation coefficients exceeding 0.99. Fireworks from five regions in China were also analyzed quantitatively, detecting heavy metals including Pb, Ba, Sr, and Ag, with recovery rates ranging from 87.9% to 107.5%. Good separation between the firework samples from different regions was achieved by using element ratios and principal component analysis (PCA). These results from the preliminary study showed that the EDTA‐assisted MPT‐MS combined with PCA is a powerful tool for characterizing firework samples and tracing them back to their sources, which is valuable to effectively regulate and manage banned fireworks. [ABSTRACT FROM AUTHOR]

Efficient water treatment ideally combines ion exchange for the removal of hardness elements and toxic trace metals as well as ultrafiltration for the removal of particulate matter. Although promising for adsorption, many high‐surface‐area polymer materials cannot be easily processed into freestanding membranes or packed bed columns, due to poor solution processability and high back pressures, respectively. The preparation of hybrid membranes comprising sulfonated hypercrosslinked polymers entrapped in nanocellulose papers is described. The hybrid membranes are effective for simultaneous ultrafiltration and ion exchange. Increasing the polymer loading of the hybrid membrane produces synergy by increasing the permeance of the membranes while enhancing the ion adsorption capacity to values exceeding those of bulk hypercrosslinked polymers. The maximum ion adsorption capacity for copper is determined to be ≈100 mg g−1 outperforming that of pure polymer (71 mg g−1) and commercially available ion exchange resins. Competitive adsorption is tested in samples containing water hardness elements and trace toxic metal ions showing high ion‐exchange capacities. Even when fully loaded with water hardness elements, Ba2+ and Sr2+ are still removed from solution. [ABSTRACT FROM AUTHOR]

Two novel hydrophobic deep eutectic solvents (HDESs), composed of alkyl (=Hexyl, Nonan) ethylenediaminium and menthol (Men), namely Hexen/Men and Nonen/Men, were synthesized. Hexen and Nonen primarily act as hydrogen bond acceptors, with Men serving as the principal hydrogen bond donor. After the formation of HDES, the IR absorption peaks of Hexen, Nonen's–NH2, and Men–OH fused into a wider peak, the 1H-NMR spectra of Men–OH, shifted to a lower field. Furthermore, a significant redshift approximately 300 cm−1 was detected in the vibrational frequency of the Men–OH functional group when performing density functional theory (DFT) calculations for the HDESs. These results support the development of stronger O–H···N bonds between Hexen/Nonen–NH2 and Men–OH, and the calculated sum of hydrogen bonding energy was approximately 56 mol·kg–1, categorizing it as an intermediate-strength hydrogen bond. Both HDESs have ethylenediamine polar heads in their hydrogen bond acceptors, which have chelating characteristics that help them coordinate with transition metal ions. Metal ions such as Cu(II), Co(II), and Ni(II) were successfully extracted from aqueous solutions at a concentration of 10 mmol·L–1using HDESs. The Cu(II) and Ni(II) extraction efficiencies exceeded 90%, indicating their effectiveness. Notably, even at higher metal ion concentrations (100 mmol·L–1), the extraction efficiencies of all three metal ions remained consistently below 80%. This indicates that the HDESs can suitably collect trace metal ions. [ABSTRACT FROM AUTHOR]

With the development of industry and agriculture, eutrophication caused by increasing amounts of phosphorus in the environment has attracted people's attention. On the other hand, copper tailings (CT) is a kind of solid waste with large quantity, large area, and easy to cause groundwater and soil pollution. CT is also a potential resource because of its large specific surface area. CT is intended to be used as an adsorbent for removal phosphate in water, but trace heavy metals and a small amount of phosphate in CT may bring negative effects. Calcium hydroxide (Ca(OH)2) was used to modify CT (CCT), hoping to fix the heavy metals and phosphate in CT at the same time. It was found that the removal capacity of CCT was significantly higher than that of CT. The process of phosphate removal by CCT involves electrostatic sorption and surface precipitation, and there is a synergistic effect between CT and Ca(OH)2. The phosphate removal rate of CCT-0.4 increased with the increase of pH value under alkaline conditions. The XRD patterns of phosphate sorption by CCT mean that Ca3(PO4)2, Ca5(PO4)3(OH) and AlPO4 exist in CCT after phosphate removal, indicating that surface precipitation occurs during the removal process. In summary, the removal mechanism of phosphate by CCT is mainly electrostatic attraction and surface precipitation. [ABSTRACT FROM AUTHOR]

This study focused on treating acid mine drainage (AMD) from a Zn-sulfide mine with a composition that includes Al = 445 mg/L, Fe = 263 mg/L, Mn = 364 mg/L, Cd = 2.8 mg/L, and Zn = 4,830 mg/L. After treatment with regional alkaline minerals, the pH increased from 3.0 to 6.3 and metal concentrations decreased mainly by precipitation, falling below Mexico's permissible limits (MPL) for river discharges, except for Cd2+ and Zn2+, which exceeded their MPLs with concentrations of 0.4 and 1,110 mg/L, respectively. We tested the use of waste materials from a Mn mine containing Mn carbonates (R3) and Mn oxides (R6) for removal of these contaminants. Several Mn oxides have been reported as promising adsorbents and indeed the R6 waste was more efficient than the R3. At a ratio of 0.75 g/L of R6, with 30 h of contact or a ratio of 0.2 with 60 h of contact, Cd2+ and Zn2+ concentrations were decreased to below their MPLs. The evaluation of removal mechanisms was hindered by the complexity of the waste's composition. However, contact with the AMD increased the zeta potential from negative to positive values, indicating a cation sorption process. Mn wastes can be used without prior alkaline mineral treatment, but their technical and economic viability is less. The results suggest that this process is suitable for treating AMD at abandoned mines sites. Additionally, the Mn wastes can potentially be sold as a sorbent material for other processes, offering a recycling option. [ABSTRACT FROM AUTHOR]

Natural radioactivity and trace elements content of two brands of shaving power that are commonly used by men were determined, in order to evaluate their radiological effect and health risk. The activity concentrations of the radionuclides were measured using gamma spectrometer equipped with calibrated NaI(Tl) detector system while the trace metals were measured using atomic absorption spectrophotometric (AAS) and energy dispersive x-ray fluorescence (ED-XRF) techniques. The averaged activity concentrations of 238U, 232Th and 40K were 2445.97 ± 9.29 Bq kg-1, 315.16 ± 17.72 Bq kg-1 and 50.45 ± 1.79 Bq kg-1 for 40K, 232Th and 238U, respectively. The equivalent dose had a mean value of 2.94 mSv year-1. The results of the trace elements analysis from both AAS and ED-XRF showed that iron had the highest concentration while selenium had the least concentration. ED-XRF showed a better recovery of the trace elements than AAS. The levels of the radionuclides identified were above the normal background for humans and the average concentrations of most of the trace metals were also above the permissible exposure limits, which can constitute health hazard to users of the shaving power. [ABSTRACT FROM AUTHOR]

Wearable sensors for sweat trace metal monitoring have the challenges of effective sweat collection and the real-time recording of detection signals. The existing detection technologies are implemented by generating enough sweat through exercise, which makes detecting trace metals in sweat cumbersome. Generally, it takes around 20 min to obtain enough sweat, resulting in dallied and prolonged detection signals that cannot reflect the endogenous fluctuations of the body. To solve these problems, we prepared a multifunctional hydrogel as an electrolyte and combined it with a flexible patch electrode to realize real-time monitoring of sweat Zn2+. Such hydrogel has magnetic and porous properties, and the porous structure of hydrogel enables a fast absorption of sweat, and the magnetic property of the addition of fabricated Fe3O4 NPs not only improves the conductivity but also ensures the adjustable internal structures of the hydrogel. Such a sensing platform for sweat Zn2+ monitoring shows a satisfied linear relationship in the concentration range of 0.16–16 µg/mL via differential pulsed anodic striping voltammetry (DPASV) and successfully detects the sweat Zn2+ of four volunteers during exercise and resting, displaying a promising path for commercial application. [ABSTRACT FROM AUTHOR]

Sebkhat Soliman included in the Ramsar Convention is a wetland of international importance. This area is of great ecological interest considering the quality and the richness of the flora and the diversity of the avifauna. This site receives a large amount of water through the EL Bey River. In order to assess the levels of contamination, concentrations of six heavy metals, including Cr, Cu, Pb, Ni, Mn, and Zn, were examined in 25 surface sediment samples from El Bey Wadi. These concentrations, which were expressed in mg/kg of dry weight, showed that Pb ranged from 5.52 to 41.66, Zn from 26.94 to 1471.89, Cu from 91.97 to 260.05, Ni from 9.35 to 140.45, Cr from 25. It's important to note that the highest metal concentrations have been found in site 5 which is frequently exposed to local industrial pollutant sources and in sites that are frequently inundated by river water that is carrying away industrial waste from the cities of Grombalia and Bou-Argoub. The mean EF values for Cu, Mn and Ni were between 3 and 5 in the sediments of the El Bey River, suggesting moderate enrichment, while the mean EF values for Pb, Zn and Cr indicating respectively moderate to severe enrichment and very severe enrichment. CF values for Cr, Cu and Zn were > 6 in sediments taken from the fifth site, which denotes a very high contamination by these metals. At site 5, PLI value (4.09), reflecting that its sediment is heavily polluted. Hierarchical cluster analysis-based complementary statistical methods have demonstrated that Mn is lithogenic and other analyzed metals are anthropogenic. [ABSTRACT FROM AUTHOR]

In this work, the seven-step extraction procedure (SSEP) proposed by our laboratory team was modified to reduce the number of fractions from seven to five (FSEP) without affecting its effectiveness. By this way, the modified SSEP was investigated by comparing the quantity of trace (Cd, Co, Cr, Cu, Ni, Zn) and major (Ca, Fe, Mn) elements leached from two sediments (TH2 and T16). Compared to the SSEP, the shortened sequential test allows to reach the same results in terms of reproductibility. Results confirm that the water-soluble step is negligeable and can be omitted for the sediments. The percentage of the total leached elements Ca, Cd, Co, Cr, Cu, Fe, Mn, Ni and Zn were 23%, 13%, 58%, 55%, 92%, 63%, 81%, 65% and 80%, respectively, for both procedures SSEP and FSEP. However, merging the reducible fractions revealed for some elements a little reduction of the leached quantities in comparison to the original SSEP. Over reducible fraction, the leached Fe element in T16, achieves 4% for SSEP and 3% for FSEP. This was explained by the partial dissolution of the amorphous and crystalline irons. Based on the reduced number of fractions, the used extraction filters (28 Vs 20) and the extraction time (18 h Vs 13.5 h), FSEP appeared to be easier for manipulation without loss of its effectiveness. However, the choice of the FSEP must be deduced from the physicochemical properties of the sample and the aim of the envisaged study. [ABSTRACT FROM AUTHOR]

To gain insights into the spatial distribution, ecological risk and origins of heavy metals in surface sediments of lacustrine ecosystems in Cameroon, the content of 7 trace metals (Fe, Cr, Zn, Cu, Ni, Pb and Cd) in sediments from 60 sampling stations in 5 lacustrine environments of different formation contexts. The selected metals were investigated based on inductively coupled plasma mass spectrometry. The results revealed that the average concentrations of Cr, Cu and Cd were higher than the geochemical Threshold values. On the basis of the spatial variation, the studied metals vary quantitatively in the following order: Fe > Cr > Zn > Cu > Ni > Pb > Cd. The calculated enrichment factor (EF) and geo-accumulation index (Igeo) showed that, sediments from large cities and industrial sites had moderate enrichment (3 < EF ≤ 5) and were moderately to severely contaminated (2 < Igeo < 3) while those from low population and rural areas had minor enrichment (1 < EF ≤ 3) and were moderately contaminated (1 < Igeo < 2). With regards to cumulative pollution, the pollution load index (PLI) and the sediment pollution index (SPI) coupled with the potential ecological risk factor (Er) and the potential ecological risk index (RI), the sediments of the lakes are polluted (SPI and PLI > 1) to some extent but with a low ecological risk (Er < 40 and RI < 150). The results of Pearson correlation, principal component analysis (PCA), and cluster analysis (CA) identified three main sources: Ni would have a natural source; Pb from anthropogenic sources, and the other metals (Fe, Cr, Zn, Cu, and Cd) could have a mixed source (anthropogenic and natural). These findings serve as a scientific foundation for the advancement and use of these lake environments, which are the most attractive sites. [ABSTRACT FROM AUTHOR]

This study was conducted in a greenhouse pot experiment to assess the effects of biochar (BC) or activated carbon (AC) alone or in combination with arbuscular mycorrhizal fungus (AMF) Glomus mosseae or acid-producing bacteria (BA) Bacillus polymyxa on plant growth, EDTA-extractable Cd and Pb, and contents of heavy metals (Cd and Pb) and nutrients (Ca, Mg, K, and P) in maize (Zea mays L.) grown on sewage wastewater contaminated soil. The results showed that most treatments with BC, AC, or its co-application with microbial inoculation led significantly to greater nutrient uptake and promoted growth of maize than non-treated plants. Additionally, the soil additives used decreased the amounts of EDTA-extractable Cd (by 28.7%-100%) and Pb (by 22.8%-94.3%). The applied treatments caused significant decreases in Cd concentrations and the bioconcentration factor (BCF) of Zea mays. The highest shoot Cd reduction was observed for AC (53%), followed by AC+BA (36.9%) > AMF (34.5%) > AC+AMF (28.5) > BA (28.3%) > BC+BA (26.1%) > BC (22.7%). However, more Cd was accumulated in the roots of plants treated with AMF by 63.7% with a lower value of translocation factor (TF) compared to control soil. In contrast, the treatments increased the levels of Pb in the maize plants, and BC coupled with AMF showed the greatest Pb accumulation. It could be concluded that the investigated additives can be applied as immobilizing agents for Cd in the soil but maize plants as phytoextractants for both metals in sewage-contaminated soil are not feasible, as indicated by insufficient phytoextraction efficiency. [ABSTRACT FROM AUTHOR]

Pollution in the Noyyal river is a well-known and documented issue and recently, heavy metal contamination has become a serious issue requiring immediate attention. So, to understand the severity of heavy metal contamination in the surface water and sediments of the Noyyal river, a comprehensive study was conducted. About 27 surface water samples and 25 sediment samples were collected at different sites along the Noyyal river. The concentrations of heavy metals were determined using inductively coupled plasma mass spectrometry (ICP-MS). The Noyyal river's surface water showed significant variations with nickel (Ni), copper (Cu), and zinc (Zn) concentrations exceeding acceptable limits for irrigation and aquatic life. Lead (Pb) concentrations were within acceptable limits for irrigation but potentially harmful to aquatic organisms. Noyyal river sediments also contained varying concentrations of chromium (Cr), copper (Cu), nickel (Ni), zinc (Zn), and gallium (Ga). Various assessment indices were employed to assess the eco-biological and human health risks associated with heavy metal contamination. The results highlighted alarming ecological and biological risks due to the accumulation of trace metals. Sediments exhibited high ecological risk (ERI values ranging from 43.81 to 371.43), while surface water samples intended for irrigation and aquatic purposes displayed extreme risks (ERI values exceeding 1200) to agricultural crops and aquatic organisms. The probability of toxicity to aquatic organisms, particularly benthic communities, was over 76% according to the biological risk assessment. The study also identified potential non-carcinogenic risks associated with metals like chromium (Cr), copper (Cu), nickel (Ni), and zinc (Zn) in the sediments. Moreover, elevated levels of Cr, Ni, and Cu in both sediments and surface water were likely to pose significant carcinogenic risks to exposed adults. Additionally, the heavy metal toxicity load in both surface water and sediments exceeded permissible limits, highlighting the urgent need for efficient removal strategies. [ABSTRACT FROM AUTHOR]

The anomalous increases or deficits in the human body can be detected by the development of accurate and sensitive methods for metal quantification in low-level concentrations. Two digestion procedures have been tested on whole blood samples for use in inductively coupled plasma optical emission spectrometry trace metal analysis (ICP-OES). The two procedures are, (microwave digestion with nitric acid and hydrogen peroxide), and (simple dilution digestion with nitric acid, N-butanol, and Triton X-100). According to the findings, the overall recoveries of all determining metals for the microwave digestion were in the range of (96%) of the expected levels, whereas for simple dilution digestion they were in the range of (85–88%) of the expected levels. The results showed a significant difference in the recovery ratios in favor of lead (Pd) and cadmium (Cd) between simple dilution and microwave digestion procedures. The findings also show that the content of these metals may be reliably measured using simple dilution and microwave digestion procedures. Abbreviations: ICP-OES: Induction coupled optical emission spectroscopy; LOD: Limit of detection; LOQ: Limit quantification; AAPCC: American Association of Poison Control Centers; NAUSS: Naif Arab University for Security Sciences; %RSD: Relative standard deviation). [ABSTRACT FROM AUTHOR]

Concentrations of toxic metals (Hg, Pb, and Cd) were determined in the muscles of Lepomis macrochirus, Barbus callensis, and Barbus nasus caught from the Moulouya River of Morocco by graphite furnace (for Pb and Cd) and cold vapour (for Hg) atomic absorption spectrometry, after acid digestion. Although the concentration of metals in some species was relatively high, no health risk has been identified in comparison to the maximum limits as set by the European Commission. The order of increasing concentrations was Cd < Hg < Pb. Calculated Target Hazard Quotients and Hazard Indices were below 1, indicating that the intake of metals via consumption of the muscles of both fish species does not represent a hazard to human health. [ABSTRACT FROM AUTHOR]

Multi-channel dilution analysis (MCDA) is a new calibration method that performs multiple dilutions of a standard solution as it makes its way from an autosampler to an analytical instrument. MCDA is based on the standard dilution analysis (SDA) method that combines the traditional standard additions and internal standardization calibration methods, correcting for both matrix interferences and fluctuations in signal levels associated with variations in the sample environment. Analysts operate the instrument in the normal manner, as all dilutions are performed automatically by splitting the sample stream entering the instrument into multiple channels of different tubing diameters and lengths. This setup results in a signal "stairstep" as portions of solution are measured at different points in time. A calibration curve is prepared from the plateau regions of the signal stairstep. MCDA has been exhibited using inductively coupled plasma optical emission spectrometry, which is a workhorse for the determination of trace metals in solution. However, MCDA is applicable for any analyte of interest in any sample type, as long as the selected measurement technique accepts samples as a flowing liquid stream. MCDA is applied to the analysis of three certified reference materials by inductively coupled plasma optical emission spectrometry (ICP-OES). Percent recoveries for a suite of analytes range from 87--106%, with relative standard deviations on the order of 1%. MCDA simplifies the analysis process, increasing sample throughput by significantly decreasing the time required for solution preparation. [ABSTRACT FROM AUTHOR]

Fish constitutes the main protein source for the Amazonian population. However, the impact of different anthropogenic activities on trace element and metal accumulation in fish and their risks for human health at a regional scale remain largely unexplored. Here we assessed exposure levels of 10 trace elements and metals (Cr, Mn, Fe, Ni, Cu, Zn, As, Cd, Pb, and Hg) in 56 samples belonging to 11 different species of fish from the Brazilian Amazon. We studied the relationship between exposure levels, fish origin, and fish feeding habits, and assessed toxicological and carcinogenic risks for the Amazonian population. No significant correlation was found between sampling site and exposure levels to the studied elements, but a significant difference was found between the accumulation of some metals and the position of the fish species in the food chain. The concentrations of Cr and Hg in fish flesh were found to exceed the Brazilian limits for human consumption. This study shows that current fish consumption patterns can lead to estimated daily intakes of Hg, As and Cr that exceed the oral reference dose, thus posing a toxicological concern. Furthermore, carcinogenic risks may be expected due to the continued exposure to Cr and As. The results of this study show that the consumption of wild caught fish in the Amazon region should be controlled. Moreover, continued monitoring of trace element and metal contamination in fish and on the health of the Amazonian population is recommended, particularly for riverine and indigenous communities. [Display omitted] [ABSTRACT FROM AUTHOR]

Two strains of Fe/Mn oxidizing bacteria tolerant to high concentrations of multiple heavy metal(loid)s and efficient decontamination for them were screened. The surface of the bio-Fe/Mn oxides produced by the oxidation of Fe(II) and Mn(II) by Pseudomonas taiwanensis (marked as P4) and Pseudomonas plecoglossicida (marked as G1) contains rich reactive oxygen functional groups, which play critical roles in the removal efficiency and immobilization of heavy metal(loid)s in co-contamination system. The isolated strains P4 and G1 can grow well in the following environments: pH 5-9, NaCl 0-4%, and temperature 20-30°C. The removal efficiencies of Fe, Pb, As, Zn, Cd, Cu, and Mn are effective after inoculation of the strains P4 and G1 in the simulated water system (the initial concentrations of heavy metal(loid) were 1 mg/L), approximately reaching 96%, 92%, 85%, 67%, 70%, 54% and 15%, respectively. The exchangeable and carbonate bound As, Cd, Pb and Cu are more inclined to convert to the Fe-Mn oxide bound fractions in P4 and G1 treated soil, thereby reducing the phytoavailability and bioaccessible of heavy metal(loid)s. This research provides alternatives method to treat water and soil containing high concentrations of multi-heavy metal(loid)s. [Display omitted] [ABSTRACT FROM AUTHOR]

Dams and their environment, interrelate with a degree of complexity that often affects the availability of potable water. In Nigeria, dams are an important source of drinking water in many communities but are vulnerable to contamination from different sources. This study assessed the possible elemental (Cd, Cr, Cu, Fe, Ni, Pb, Mn, and Zn) contamination sources of selected dams in a total of 126 samples comprising 54 surface water, and 72 sediment samples collected from six main dams in Osun State using multivariate analyses like Principal Component Analysis (PCA) and Cluster Analysis (CA). Generally, the average elemental concentration was in the decreasing order of Cr > Ni > Cd > Pb > Cu > Fe > Zn > Mn and Pb > Cr > Ni > Cd > Zn > Mn > Fe > Cu for surface water and sediment samples respectively. Furthermore, statistical analysis showed that the average concentrations of the potentially toxic elements (PTEs) did not differ significantly (p < 0.05) across the sampling sites, indicating similar PTEs profiles. The PCA and CA revealed possible sources of elemental contamination to the dam quality as weathering of bedrocks, uncontrolled farming activities, abandoned equipment, boat fueling, maintenance, and repairs. Although only 13.9% of the hazard quotients (HQ) were higher than one for all the studied heavy metals in surface water, 91.7% of the hazard index (HI) were higher than one. This suggests an unacceptable risk of non-carcinogenic effects from the direct consumption of dam water. Furthermore, the oral target cancer risk, TCRoral in children > adults and > 1 × 10−4 for cancer risk set by USEPA, however, the % contribution of Cr to ∑TCRoral in adults which is > 1 × 10−4 ranged between 98.9 to 99.5%, indicating that Cr is the most dominant carcinogens in the overall cancer risk in adults. [ABSTRACT FROM AUTHOR]

In the context of the European Critical Raw Materials Act, this work attempts to demonstrate the potential of residual material flows from non-ferrous metallurgy and their possible contribution to the supply security of metals by locally available new secondary resources, assuming technically and economically viable processing. Based on the aluminium, zinc, copper and lead industries, the resulting waste streams are discussed and, in particular, the complex process consisting of physical, chemical and metallurgical steps is described. Their diversity, be it slags, dusts or even sludges, has a wide variety of morphologies and compositions due to the process of generation. In the past, many concepts for reprocessing were investigated, but the goal was usually only the recovery of one target element or to avoid landfilling by using it, for example, as a building material, whereby the metals contained are completely lost. If the target is the extraction of valuables, the required interdisciplinary process development must be based on an in-depth characterization to understand the behaviour of metals and trace elements in possible extraction steps and also to develop suitable strategies for influencing the behaviour of target elements with the aim of extraction. This starts with an in-depth comprehension of the formation process, which is the subject of this article and has a direct influence on the composition and morphology of the materials, thus forming the basis for understanding the behaviour in potential recycling processes. Furthermore, typical compositions of the residual material streams, sources and, if available, quantities are shown and, in summary, an attempt is made to evaluate the materials in a SWOT analysis and to address the challenges in developing extraction steps for processing. While mine tailings are mostly found outside of Europe, the potential of the residual materials from metallurgy is local due to the processing of the concentrates in Europe. This leads to several potential advantages in a possible reprocessing, such as no or shorter transport routes, which is linked to lower quantity of emissions, defined volume and known composition, no geopolitical risk, conservation of primary resources, and increasing Europe's sustainability through a more comprehensive use of the raw materials. This article is part of the discussion meeting issue 'Sustainable metals: science and systems'. [ABSTRACT FROM AUTHOR]

Nickel stable isotopes (δ60Ni) provide insight to Ni biogeochemistry in the modern and past oceans. Here, we present the first Pacific Ocean high‐resolution dissolved Ni concentration and δ60Ni data, from the US GEOTRACES GP15 cruise. As in other ocean basins, increases in δ60Ni toward the surface ocean are observed across the entire transect, reflecting preferential biological uptake of light Ni isotopes, however the observed magnitude of fractionation is larger in the tropical Pacific than the North Pacific Subtropical Gyre. Such surface ocean fractionation by phytoplankton should accumulate isotopically lighter Ni in the deep Pacific, yet we find that North Pacific deep ocean δ60Ni is similar to previously reported values from the deep Atlantic. Finally, we find that seawater dissolved δ60Ni in regions with hydrothermal input can be either higher or lower than background deep ocean δ60Ni, depending on vent geochemistry and proximity. Plain Language Summary: A habitable Earth relies on the growth of microscopic plants, called phytoplankton, in the ocean. Phytoplankton help regulate Earth's climate and their growth requires various nutrients in seawater, including a suite of metal elements such as iron, zinc, and nickel (Ni). These metals are called trace metals in the ocean because their concentrations are extremely low in seawater, yet they are essential micronutrients. Therefore, it is important to understand how much and how these elements are supplied to and removed out of the ocean, and how they are used by phytoplankton. To study this question, we analyzed Ni isotope ratios of hundreds of seawater samples collected from the Pacific Ocean—which is the ratio of naturally occurring Ni atoms with different numbers of neutrons and therefore slightly different masses. We find that surface seawater is more enriched in heavier Ni isotopes than the deep seawater, in particular around the tropical Pacific. The deep ocean has similar Ni isotope ratios across different ocean basins, from the Atlantic to the Pacific. Seawater Ni isotope ratios are impacted by rivers near Alaska, submarine volcanos near Hawaiʻi, and a submarine volcanic chain called the East Pacific Rise. Key Points: Enrichment of heavier Ni isotopes is observed in the surface ocean across the GP15 transect, particularly in the equatorial PacificNorth Pacific deep ocean Ni isotope composition is nearly homogeneous and similar to previously reported values from other ocean basinsHydrothermal activity can both decrease and increase seawater Ni isotope composition, depending on vent geochemistry and proximity [ABSTRACT FROM AUTHOR]