Search Results (407)

Protected areas are essential for conserving biodiversity and sustaining ecosystems, yet their effective management requires a clear understanding of soil and water quality, which underpin ecological processes. This study evaluated 15 soil and seven water samples to assess their physico-chemical properties, focusing on heavy metal concentrations. Results showed that soils were generally neutral to alkaline, with Hashwan-2 exhibiting the highest concentrations of calcium (26.5 meq/L), magnesium (11.2 meq/L), carbonates (0.32 meq/L), bicarbonates (3.66 meq/L), and chloride (35.43 meq/L). Heavy metal analysis indicated elevated nickel (51.628 mg/kg) and chromium (76.29 mg/kg) at Albuyitlar-2, and chromium (68.015 mg/kg) at Shabak-Mateam-1 1 1, exceeding US-EPA permissible limits of 45 mg/kg for nickel and 64 mg/kg for chromium. Water samples revealed high levels of aluminum (12.681 mg/L), manganese (0.146 mg/L), and iron (7.055 mg/L), also exceeding the US-EPA thresholds of 0.2, 0.1, and 0.5 mg/L, respectively. In contrast, more toxic metals such as arsenic, cadmium, lead, and mercury remained within safe limits. These findings highlight localized concerns regarding heavy metal contamination that warrant continued monitoring to ensure ecosystem health. Full article

The impact of prenatal exposure to trace metal mixtures on children’s neurodevelopment remains debated. Many studies treat all trace metals as a single entity, overlooking the distinct biological roles of essential and toxic metals. This approach may highlight overall exposure but fails to capture their differential effects on neurodevelopment. This study aims to examine the associations between prenatal exposure to essential and toxic metals and children’s cognitive development, focusing on their independent effects. A cohort of 201 mother–infant pairs was analyzed. Maternal urinary metal levels were measured at 12 weeks of gestation, and children’s neurodevelopment was assessed at 4 years using the Wechsler Preschool and Primary Scale of Intelligence and the Developmental Neuropsychological Assessment. Generalized Additive Models (GAM), Restricted Cubic Spline (RCS), and Weighted Quantile Sum (WQS) regression were applied. GAM identified non-linear associations between essential metals (manganese and molybdenum) and cognitive outcomes, including verbal comprehension index (VCI), working memory index, full-scale IQ, and general ability index, which were confirmed by RCS. No non-linear relationships were observed for toxic metals. WQS showed negative associations between toxic metals and VCI (b = −1.07), processing speed index (b = −0.98), vocabulary acquisition index (b = −1.25), and verbal fluency (b = −0.23), mainly driven by cadmium (Cd) and antimony (Sb). Essential metal mixtures were not associated with cognitive outcomes. Prenatal exposure to toxic metals negatively affects children’s cognitive and neuropsychological development. Reducing maternal exposure during pregnancy is essential for protecting offspring development. Full article

Lithium-ion batteries (LIBs) are vital for modern energy storage applications. Lithium iron phosphate (LFP) is a promising cathode material due to its safety, low cost, and environmental friendliness compared to the widely used nickel manganese cobalt oxide (NMC), which contains hazardous nickel and cobalt compounds. However, challenges remain in enhancing the performance of LFP cathodes due to their low electronic and ionic conductivity. To improve both the safety and sustainability of the battery, this work presents a water-based LFP cathode utilizing the bio-based binder carboxymethyl cellulose (CMC), eliminating the need for polyvinylidene fluoride (PVDF) and the toxic solvent N-methyl-2-pyrrolidone (NMP). This study investigates the impact of different dispersing methods—dissolver mixing and wet jet milling—on slurry properties, electrode morphology, and battery performance. Slurries were characterized by rheology, particle size distribution, and sedimentation behavior, while coated and calendered electrodes were examined via thickness measurements and scanning electron microscopy (SEM). Electrochemical performance of the electrodes was evaluated by means of C-Rate testing. The results reveal that dispersing methods significantly influence slurry characteristics but marginally affect electrochemical performance. Compared to dissolver mixing, wet jet milling reduced the median particle size by 39% (ΔD50 = 3.1 µm) and lowered viscosity by 96% at 1 s⁻¹, 80% at 105 s⁻¹, and 64% at 1000 s⁻¹. In contrast, the electrochemical performance of the resulting electrodes differed only slightly, with discharge capacity varying by approximately 12.8% at 1.0 C (Δcapacity = 10.7 mAh g⁻¹). This research highlights the importance of optimizing not only material selection but also processing techniques to advance safer and more sustainable energy storage solutions. Full article

Over the next 5–10 years, the feedstock to lithium-ion battery recycling facilities will shift from Co- and Ni-rich chemistries to lower-value battery chemistries, such as lithium iron phosphate (LFP). Traditional recycling processes use toxic and corrosive inorganic acids for leaching, generating toxic waste streams. The low-value feedstocks will be LFP-rich with contamination from lithium cobalt oxide (LCO) and lithium–nickel–manganese–cobalt oxide (NMC) battery chemistries. Overall, the lower-value feedstock coupled with the need to reduce environmentally damaging waste streams requires the development of robust, green leaching processes capable of selectively targeting the LFP and LCO/NMC battery chemistries. This research concluded that a first-stage oxalic acid leach could selectively extract Al, Li, and P from the industrially sourced LFP-rich black mass. When operating at the optimal conditions (0.5 M oxalic acid, 5% solids, pH 0.8, and an agitation speed of 600 rpm), >99% of the Li and P and >97% of the Al were selectively extracted after 2 h, while Mn, Fe, Cu, Ni, and Co extractions were kept relatively low, namely, at 19%, <3%, <1%, 0%, and 0%. This research also explored a second-stage leach to treat the first-stage leach residue using ascorbic acid, citric acid, and glycine. It was concluded that when leaching with glycine (30 g/L glycine, a temperature of 40 °C, an agitation speed of 600 rpm, and 2% solids at pH 9.6), that >97% of the Co, >77% of the Ni, and 41% of the Mn were extracted, while the co-extraction percentages of Cu, Fe, and Al were <27%, <4%, and <2%. Full article

In this study, both trivalent and hexavalent forms of chromium were examined in urban and agricultural Mediterranean soils. Chromium partitioning in different soil fractions was studied. Pot experiments included contamination of soil samples using Cr solutions, as well as a further study regarding Cr distribution in naturally contaminated soils. The soils were subjected to quantitative determination of both the available and total Cr concentration, as well as Cu and Zn, which were naturally present in the soil samples. Metal concentrations in the soil fractions were quantified after the application of the BCR fractional extraction method. The numbers of both trivalent and hexavalent Cr ions in each extract were determined. Considerable discrepancies were noticed regarding the Cr content of each soil fraction in both municipal and cultivated soils, indicating the possible origin of the pollution. The increasing impact of pollution is a significant parameter for the availability of chromium ions in both agricultural and urban soils. Increased pollution durations resulted in a significant increase in the non-available fraction of toxic Cr (VI), mainly in urban soil. Variations were also observed in the chromium species, as changes in soil parameters and in the conditions of the experiment seem to affect the conversion of the less harmful trivalent chromium to the toxic hexavalent chromium. In urban soils, the amount of toxic Cr (VI) bound to iron and manganese oxides exceeds 37.8%, while in agricultural soils, the amount of Cr (VI) associated with soil organic matter reaches 35%. Knowing the mechanisms and variables influencing Cr availability in agricultural and urban Mediterranean soils is desirable, as safe living in ecologically acceptable fields and producing safe goods in healthy soil systems are paramount goals. Full article

Spirulina and Chlorella are nutrient-rich microalgae widely consumed as dietary supplements; however, their high biosorption capacity raises concerns regarding the accumulation of environmental contaminants. This study analyzed 52 commercially available Spirulina and Chlorella products (29 conventional, 23 organic) to assess the co-occurrence of heavy metals and pharmaceutical residues, as these two classes of contaminants represent distinct yet complementary indicators of environmental pollution—heavy metals reflect long-term inputs from natural and industrial sources, while pharmaceuticals signal more recent contamination linked to human activity and wastewater discharge. To the best of our knowledge, this is the first study to investigate the presence of pharmaceutical residues—including cardiovascular drugs, antidepressants, antibiotics, and sulfonamides—in both conventional and organic formulations of microalgae-based dietary supplements. The analyses were performed using Inductively Coupled Plasma Mass Spectrometry and liquid chromatography coupled to tandem mass spectrometry. Aluminum, manganese, strontium, and zinc were the dominant trace elements. All samples complied with EU regulatory limits for toxic metals. More importantly, a wide range of pharmaceutical residues was detected in the supplements. Caffeine was the most frequently found compound, followed by metronidazole, carbamazepine, benzocaine, and tramadol. Particular concern is raised by the calculated TWI (% of tolerable weekly intake) for aluminum. Principal Component Analysis revealed significant compositional differences between Spirulina and Chlorella products, with vanadium notably elevated in conventionally cultivated Spirulina. Surprisingly, no significant differences were observed between organic and conventional products within each algal type. Our findings provide a novel contribution to the field by highlighting the presence of pharmaceutical residues in microalgae-based supplements and addressing a critical knowledge gap concerning potential chronic exposure to these contaminants through dietary intake. Full article

Elevated exposure to manganese (Mn) has been linked to a broad spectrum of neurological disorders, including motor dysfunction. Neuroinflammation with excessively activated astrocytes plays a critical role in the pathogenesis and progression of neurodegenerative diseases. Astrocyte-mediated neuroinflammation plays a dual role due to distinct astrocyte phenotypes, including deleterious A1 and neuroprotective A2. Our previous studies have confirmed that Mn induces activation of astrocytes in the central nervous system, and endoplasmic reticulum (ER) stress has been verified to regulate A1 activation; however, the molecular mechanisms underlying Mn-induced neurotoxicity remain incompletely understood. We establish in vivo and in vitro Mn exposure models and observed that Mn induced A1 activation of astrocytes in both models, with upregulation of A1-specific markers. Sub-cellular morphological analysis showed Mn-induced ER stress in A1-type astrocytes. We found that EIF2α-PERK signaling pathways are activated in astrocytes and drive ER stress and mitochondrial impairment. Suppression of astrocytic PERK, using either ISRIB or GSK2606414, alleviates Mn-induced ER stress and A1 activation, which in turn mitigates the motor deficits induced by Mn exposure. These findings reveal that inhibition of PERK can ameliorate Mn-induced neurotoxicity by suppressing astrocyte activation and preserving organelle homeostasis, offering a potential therapeutic strategy to mitigate the harmful effects of Mn toxicity. Full article

The Puebla Metropolitan Area, one of the most industrialized regions in Mexico, shows severe contamination of both surface and groundwater. In this study a multi-tracer approach combining hydrochemistry with environmental isotopes (δ²H, δ¹⁸O, ³H) was applied to evaluate groundwater–surface water (GW–SW) interactions and their role in water quality degradation. Elevated concentrations of aluminum, iron, zinc, and lead were detected in the Alseseca and Atoyac Rivers, exceeding national standards, while arsenic, manganese, and lead in groundwater surpassed Mexican and WHO drinking water limits. The main sources of contamination include volcanic inputs from Popocatepetl activity (e.g., arsenic) and untreated discharges from industrial parks (e.g., lead), which together introduce significant loads of Potentially Toxic Elements (PTEs) into surface and groundwater. Isotopic analysis identified three sources for aquifer recharge: (1) recharge from high-altitude meteoric water, (2) mixed GW–SW water recharged at intermediate elevations with heavy metal presence, and (3) recharge from lower altitudes (evaporate water). Tritium confirmed both modern and old recharge, while isotope-based mixing models indicated surface water contributions to groundwater ranging from 18% to 72%. These interpretations were derived from the integrated analysis of hydrochemical and isotopic data, allowing the quantification of recharge sources, residence times, and mixing processes. The results demonstrate that hydraulic connectivity, enhanced by fractures and faults, facilitates contaminant transfer from polluted rivers into the aquifer. Full article

Capão da Roça, located in the municipality of Charqueadas, is one of the few areas of coal tailing deposits at the surface within the State of Rio Grande do Sul, Brazil that generates acid mine drainage (AMD). Over the course of 2007, the landfill was characterised in detail, and an active treatment plant involving pH neutralisation and metal precipitation operations was implemented to meet emission standards for mine water. In that year, based on the sulphur mass balance, it was estimated that the process of AMD generation would last for approximately two decades. The objective of this work was to study the temporal evolution of the parameters of the raw AMD. The effluent was analysed for 17 years on a monthly basis in regard to pH, acidity, metals (Fe, Al, and Mn), and sulphates. The results indicated an increase in pH (from 2.1 to 4.7), a decay in the concentration of metals (from 177.8 to 0.1 mg L⁻¹ for iron, 29.0 to 0.1 mg L⁻¹ for aluminium, and 3.1 to 0.6 mg L⁻¹ for manganese), sulphates (from 2023 to 307 mg L⁻¹), and acidity (from 539.5 mg CaCO₃ L⁻¹ to 3.96 mg CaCO₃ L⁻¹), which were adjusted to a first-order kinetic model in agreement with observations at some other mining sites. Over the years, the active lime neutralisation–precipitation treatment system has been efficient in treating the effluent. Today, most water quality parameters already meet emissions standards; however, the AMD treatment plant is still necessary to prevent pH fluctuations and to reduce the concentrations of manganese. For this reason, a transition from an active to a passive treatment system was considered. Pilot scale studies confirmed that channels filled with gravel-size limestone or slag enable the neutralisation/increase in the pH of the effluent and remove residual amounts of some metals, resulting in an effluent with no level of toxicity to the microcrustacean Daphnia magna. Full article

Cadmium (Cd), a pervasive and highly phytotoxic metal pollutant, poses severe threats to agricultural productivity, ecosystem stability, and human health through its entry into the food chain. Plants have evolved intricate defense mechanisms, among which the strategic manipulation of nutrient elements emerges as a critical physiological and biochemical strategy for mitigating Cd stress. This comprehensive review delves deeply into the multifaceted roles of essential macronutrient elements (nitrogen, phosphorus, potassium, calcium, magnesium, sulfur), essential micronutrient elements (zinc, iron, manganese, copper) and non-essential beneficial elements (silicon, selenium) in modulating plant responses to Cd toxicity. We meticulously dissect the physiological, biochemical, and molecular underpinnings of how these nutrients influence Cd bioavailability in the rhizosphere, Cd uptake and translocation pathways, sequestration and compartmentalization within plant tissues, and the activation of antioxidant defense systems. Nutrient elements exert their influence through diverse mechanisms: competing with Cd for root uptake transporters, promoting the synthesis of complexes that reduce Cd mobility, stabilizing cell walls and plasma membranes to restrict apoplastic flow and symplastic influx, modulating redox homeostasis by enhancing antioxidant enzyme activities and non-enzymatic antioxidant pools, regulating signal transduction pathways, and influencing gene expression profiles related to metal transport, chelation, and detoxification. The complex interactions between nutrients themselves further shape the plant’s capacity to withstand Cd stress. Recent advances elucidating nutrient-mediated epigenetic regulation, microRNA involvement, and the role of nutrient-sensing signaling hubs in Cd responses are critically evaluated. Furthermore, we synthesize the practical implications of nutrient management strategies, including optimized fertilization regimes, selection of nutrient-efficient genotypes, and utilization of nutrient-enriched amendments, for enhancing phytoremediation efficiency and developing low-Cd-accumulating crops, thereby contributing to safer food production and environmental restoration in Cd-contaminated soils. The intricate interplay between plant nutritional status and Cd stress resilience underscores the necessity for a holistic, nutrient-centric approach in managing Cd toxicity in agroecosystems. Full article

Lead (Pb) in soil poses serious environmental and health risks, and its removal requires complex and costly treatment methods to meet strict regulatory standards. To effectively address this challenge, innovative and efficient techniques are essential. Sepiolite-supported MnFe₂O₄ (MnFe₂O₄/SEP) composites were synthesized via a chemical co-precipitation method. The effects of MnFe₂O₄/SEP on soil pH, cation exchange capacity (CEC), available Pb content, Pb²⁺ uptake, and the activities of antioxidant enzymes in Brassica chinensis (Pak Choi) were examined. MnFe₂O₄/SEP showed superior Pb²⁺ adsorption compared to SEP alone, fitting Langmuir models, Dubinin-Radushkevich (D-R) models, Temkin models and pseudo-second-order kinetics. The maximum adsorption capacities at 298, 308, and 318 K were 459, 500 and 549 mg·g⁻¹, respectively. XPS analysis indicated that chemisorption achieved through ion exchange between Pb²⁺ and H⁺ was the main mechanism. MnFe₂O₄/SEP increased the soil pH by 0.2–1.5 units and CEC by 18–47%, while reducing available Pb by 12–83%. After treatment with MnFe₂O₄/SEP, acid-extractable and reducible Pb in the soil decreased by 14% and 39%, while oxidizable and residual Pb increased by 26% and 21%, respectively. In Brassica chinensis, MnFe₂O₄/SEP reduced Pb²⁺ uptake by 76%, increased chlorophyll content by 36%, and decreased malondialdehyde (MDA) levels by 36%. The activities of antioxidant enzymes—superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT)—were decreased by 29%, 38% and 17%, respectively. These findings demonstrate that MnFe₂O₄/SEP is an efficient Pb²⁺ adsorbent that immobilizes Pb in soil mainly through ion exchange, thereby providing a highly effective strategy for remediating Pb-contaminated soils and improving plant health. Full article

Reactive oxygen species (ROS) function as critical signaling molecules in cancer biology, promoting proliferation, angiogenesis, and metastasis at controlled levels while inducing lethal damage when exceeding the cell’s buffering capacity. To survive under this state of chronic oxidative stress, cancer cells become dependent on a hyperactive antioxidant shield, primarily orchestrated by the Nrf2, glutathione (GSH), and thioredoxin (Trx) systems. These defenses maintain redox homeostasis and sustain oncogenic signaling, notably through the oxidative inactivation of tumor-suppressor phosphatases, such as PTEN, which drives the PI3K/AKT/mTOR pathway. Targeting this addiction to a rewired redox state has emerged as a compelling therapeutic strategy. Pro-oxidant therapies aim to overwhelm cellular defenses, with agents like high-dose vitamin C and arsenic trioxide (ATO) showing significant tumor-selective toxicity. Inhibiting the master regulator Nrf2 with compounds such as Brusatol or ML385 disrupts the core antioxidant response. Disruption of the GSH system by inhibiting cysteine uptake with sulfasalazine or erastin potently induces ferroptosis, a non-apoptotic cell death driven by lipid peroxidation. Furthermore, the thioredoxin system is targeted by the repurposed drug auranofin, which irreversibly inhibits thioredoxin reductase (TrxR). Extensive preclinical data and ongoing clinical trials support the concept that this reliance on redox adaptation is a cancer-selective vulnerability. Moreover, novel therapeutic strategies, including the expanding field of redox-active metal complexes, such as manganese porphyrins, which strategically leverage the differential redox state of normal versus cancer cells through both pro-oxidant and indirect Nrf2-mediated antioxidative mechanisms (triggered by Keap1 oxidation), with several agents currently in advanced clinical trials, have also been discussed. Essentially, pharmacologically tipping the redox balance beyond the threshold of tolerance offers a rational and powerful approach to eliminate malignant cells, defining a novel frontier for targeted cancer therapy. Full article

Sulfonamides represent a versatile class of biologically active compounds, best known for their antibacterial activity, but increasingly investigated for their potential in oncology. Free sulfonamides themselves display cytotoxic properties; however, coordination with metal ions often enhances both selectivity and potency, while also introducing new mechanisms of action. Although numerous studies have reported sulfonamide–metal complexes with anticancer activity, a systematic overview linking biological properties to the central metal atom has been lacking. This review summarizes current research on sulfonamide complexes with transition metals and selected main-group elements, focusing on their pharmacological potential as anticancer agents. The compounds discussed include complexes of titanium, chromium, manganese, rhenium, ruthenium, osmium, iridium, palladium, platinum, copper, silver, gold, iron, cobalt, nickel, uranium, calcium, magnesium and bismuth. For each group, representative structures are presented along with cytotoxicity data against cancer cell lines, comparisons with reference drugs such as for example cisplatin, and where relevant, studies on carbonic anhydrase inhibition. The survey of available data demonstrates that many sulfonamide–metal complexes show cytotoxic activity comparable to or greater than existing chemotherapeutic agents, while in some cases exhibiting reduced toxicity toward non-cancerous cells. These findings highlight the promise of sulfonamide–metal complexes as a fertile area for anticancer drug development and provide a framework for future design strategies. This review covers the research on anti-cancer activity of sulfonamide complexes during the years 2007–2025. Full article

The invasive seaweed Caulerpa cylindracea is widespread in the Mediterranean and has notable ecological impacts, yet its nutritional potential remains underexplored. This study aimed to characterize the nutritional composition of C. cylindracea comprehensively. Samples were collected from the Northern Adriatic and analyzed for proximate composition, amino acids, minerals, vitamins, and fatty acids using standardized laboratory methods. The results revealed a balanced proximate profile with notable protein (11.8 g/100 g DW) and fiber (24.4 g/100 g DW) levels and relatively low carbohydrates (11.6 g/100 g DW). The seaweed exhibited a rich mineral content, including high levels of iron, magnesium, manganese, and potassium, while toxic heavy metals were absent. Vitamins B12 and E were present at elevated concentrations compared to related species. Amino acid analysis showed a well-balanced essential amino acid profile supporting its nutritional value. The high salt content (33.8 g/100 g DW) suggests the need for desalination prior to consumption to reduce sodium intake risks. These results indicate the potential of this invasive species as a novel dietary component, particularly for populations who may benefit from plant-based marine sources of essential nutrients in the Mediterranean region. This is the first comprehensive nutritional characterization of C. cylindracea from the Adriatic Sea, highlighting its potential for valorization as both an environmental management strategy and a novel dietary resource. Full article

The surging demand for lithium-ion batteries (LIBs) has intensified the need for sustainable recovery of critical metals such as lithium, manganese, cobalt, and nickel from spent cathodes. While conventional hydrometallurgical and pyrometallurgical methods are widely used, they involve high energy consumption, hazardous waste generation, and complex processing steps, underscoring the urgency of developing eco-friendly alternatives. This study presents a novel, water-enhanced deep eutectic solvent (DES) system composed of choline chloride and D-glucose for the efficient leaching of valuable metals from spent LiMn-based battery cathodes. The DES was synthesized under mild conditions and applied to dissolve cathode powder, with leaching performance optimized by varying temperature and duration. Under optimal conditions (100 °C, 24 h), exceptional recovery efficiencies were achieved: 98.9% for lithium, 98.4% for manganese, and 71.7% for nickel. Material characterization using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and inductively coupled plasma mass spectrometer (ICP-MS) confirm effective phase dissolution and metal release. Although this DES system requires relatively higher temperature and longer reaction time compared to traditional acid leaching, it offers clear advantages in terms of non-toxicity, biodegradability, and elimination of strong oxidizing agents. These results demonstrate the potential of water-enhanced choline chloride–glucose DES as a green alternative for future development in sustainable battery recycling, supporting circular economy objectives. Full article