Search Results (488)

The influence of rootstocks on mineral nutrient composition in the edible tissue of citrus fruits has not been explored so far. This study assessed leaf and juice mineral nutrients of sweet orange (Citrus sinensis (L.) Osbeck) cultivars (‘Pusa Sharad’ and ‘Pusa Round’) grafted onto different rootstocks (‘RLC-6’, ‘C-35’, ‘X-639’, ‘Yamma Mikan’, ‘Soh Sarkar’, ‘RLC-7’, and ‘Jatti Khatti’). Deviation from optimum percentage (DOP) index was employed as an integrative measure to assess leaf mineral nutrient balance for specific scion–rootstock combinations. The relative abundance of leaf mineral nutrients was ranked as follows: Ca > K > P > S > Mg > Na > Fe > Mn > Zn > Cu. Overall, rootstock ‘X-639’ demonstrated superior mineral nutrient uptake efficiency across grafted plants of both scion cultivars, as indicated by higher leaf mineral nutrient concentrations. Juice mineral nutrient concentrations followed the order K (930.87–1362.17 mg L⁻¹), Ca (346.40–651.33 mg L⁻¹), P (116.23–236.97 mg L⁻¹), Mg (64.60–102.50 mg L⁻¹), S (49.35–74.34 mg L⁻¹), Na (25.61–47.88 mg L⁻¹), Fe (4.76–7.92 mg L⁻¹), Zn (1.79–4.34 mg L⁻¹), Mn (0.73–1.62 mg L⁻¹), and Cu (0.41–0.71 mg L⁻¹), indicating distinct differences in the accumulation pattern of macro- and micro-mineral nutrients in the edible tissues across the studied scion–rootstock combinations. Multivariate analysis revealed that the rootstocks significantly influenced juice mineral nutrient levels, indicating rootstock-mediated agronomic biofortification. Rootstock ‘RLC-6’ enhanced juice K levels, and ‘Soh Sarkar’ improved juice Mg contents, while ‘X-639’ improved juice micronutrient (Zn, Mn, Cu) accumulation in both cultivars. This study constitutes the first comprehensive investigation that explicitly evaluates the influence of rootstocks on the enhancement of mineral nutrient content in the edible tissues of citrus fruits. It further elucidates how rootstock selection can indirectly affect dietary mineral intake, thereby highlighting its potential role for improved nutrition. Full article

A nano-CuO/ZnO desulfurizer was successfully prepared via a homogeneous precipitation method, and the effects of Cu doping on its microstructure, oxygen species, desulfurization performance, and reaction mechanism were systematically investigated. The results show that an appropriate Cu doping amount (TZ2, Cu:Zn = 1:18.40) significantly reduces the particle size (to ~10.9 nm) compared with pure ZnO (14.3 nm), leading to an increased number of surface-active sites. XPS and TG analyses reveal that Cu incorporation increases the proportion of lattice oxygen and decreases the concentration of oxygen vacancies, indicating that the modification effect of Cu dominates over the particle size effect in regulating surface oxygen species. Despite the reduced oxygen vacancy concentration, the desulfurization performance is markedly enhanced, with TZ2 exhibiting the longest breakthrough time under oxygen-free conditions at room temperature. This improvement is attributed to the strong interaction between highly dispersed Cu species and the ZnO matrix, which promotes H₂S adsorption and activation. Mechanistic studies demonstrate that, unlike pure nano-ZnO, where oxygen vacancy-mediated reactions dominate, the CuO/ZnO system follows a chemisorption-driven pathway involving the formation of copper sulfides and highly reactive polysulfide intermediates. Furthermore, the presence of oxygen significantly influences the reaction behavior, with an optimal oxygen concentration (~10%) maximizing desulfurization performance by balancing the generation of reactive oxygen species and sulfur intermediates. This work provides new insights into the design of high-performance ZnO-based desulfurizers and highlights the critical role of Cu-induced mechanism transformation. Full article

Cs₃Cu₂I₅ single crystals are regarded as promising next-generation scintillators due to their large Stokes shift and low self-absorption characteristics. However, the cost-effective solution growth method faces critical challenges: the instability of colloidal precursors in solutions and the severe oxidation of Cu⁺ during crystal growth. This study innovatively introduces yttrium chloride (YCl₃) as a dual-functional additive to address both issues simultaneously. The hydrolysis of YCl₃ creates a controlled acidic environment, effectively suppressing the oxidation of Cu⁺; meanwhile, it enhances the stability of colloidal precursors by significantly increasing their surface charge and narrowing the particle size distribution. These synergistic effects enable the rapid growth (approximately 100 h) of near-centimeter-sized Cs₃Cu₂I₅ single crystals with high crystallinity, without the need for inert gas protection. The optimized crystals exhibit exceptional performance: a photoluminescence quantum yield (PLQY) of 93.22% ± 0.47%, a scintillation decay time of 210.04 ns, and a light yield of ~738.14 pe/MeV. This YCl₃-mediated growth strategy establishes an efficient approach for the solution-based synthesis of high-quality Cs₃Cu₂I₅ single crystals, holding great significance for advancing high-sensitivity, environment-stable radiation detection applications such as medical diagnostics and nuclear safety monitoring. Full article

Metal ion-based chemo-immunotherapy is often limited by rigid intracellular metal homeostasis, insufficient reactive oxygen species (ROS) accumulation, and an immunosuppressive tumor microenvironment (TME). To overcome these limitations, we engineered an ATP-responsive, core–shell bimetallic nanoreactor (Cu/ZIF@PDA, termed CZP) featuring a precisely controlled ~25 nm biomimetic polydopamine (PDA) coating. Triggered by elevated tumoral ATP levels, CZP undergoes coordination-induced disassembly and promotes oxidative stress amplification. Specifically, the PDA shell acts as a superoxide dismutase (SOD) mimetic to continuously supply H₂O₂, fueling Cu²⁺-mediated Fenton-like reactions to unleash highly toxic hydroxyl radicals (•OH) while aggressively depleting the intracellular glutathione (GSH) pool. This irreversible oxidative damage, coupled with Zn²⁺-induced mitochondrial dysfunction, triggers profound mitochondrial DNA (mtDNA) leakage. Crucially, this cytosolic DNA robustly activates the cGAS-STING signaling axis, driving a massive surge in immunogenic cell death (ICD) and significantly promoting dendritic cell (DC) maturation. Furthermore, CZP markedly inhibited primary tumor growth in vivo and showed protection in a tumor re-challenge model, accompanied by enhanced dendritic cell maturation. These findings support the potential of this ATP-responsive bimetallic nanoplatform to promote antitumor immune activation. Full article

Amygdala dysfunction is implicated in stress-related affective disorders, and astrocytes are key regulators of amygdalar neuroplasticity. Here, we examined whether running exercise modulates astrocyte number, morphology, proliferation, and excitatory synaptic contacts in the basolateral amygdala (BLA) and central amygdala (CeA) in rats exposed to chronic unpredictable stress (CUS). Anhedonia-like behaviors were evaluated using the sucrose preference test, while anxiety-related behaviors were assessed using the elevated plus maze and open field tests. Unbiased stereological three-dimensional quantification was used to assess amygdalar volume and estimate astrocyte numbers in BLA and CeA, and immunofluorescence with morphological reconstruction was performed to quantify astrocytic complexity, proliferation, and astrocyte-associated PSD95⁺ puncta. Running exercise significantly increased sucrose preference in CUS rats, whereas elevated plus maze and open field measures were not significantly changed. CUS reduced astrocyte number and proliferation, and induced astrocytic morphological atrophy in both subregions. These alterations were reversed by running. Moreover, running increased the number of excitatory synapses contacted by astrocytes in the BLA and CeA of CUS rats. These findings suggest that running promotes astrocyte-mediated structural remodeling in amygdalar subregions, which may contribute to the regulation of anhedonia-like behavioral alterations associated with chronic stress. Full article

Oral squamous cell carcinoma (OSCC) remains a major clinical challenge, highlighting the need for novel therapeutic strategies. Natural bioactive compounds such as curcumin (Cu) and cordycepin (Co) have shown anticancer potential; however, their effects on cancer cell morphology and behavior remain incompletely characterized. This study assessed the individual and combined effects of Cu and Co on oral squamous cell carcinoma cells (OECM-1) and normal human gingival epithelial cells (HGEpiC) over 24 and 48 h. Metabolic activity, membrane integrity, oxidative stress, apoptosis, and inflammatory responses were evaluated using MTT, LDH, ROS-H₂O₂, caspase 3/7, and NO assays. Label-free digital holographic microscopy enabled real-time monitoring of morphology, motility, and proliferation. Both compounds induced ROS-mediated cytotoxicity, but responses were notably more pronounced in OECM-1 than in HGEpiC cells. Real-time morphological profiling revealed distinct response patterns: Co primarily exerted cytostatic effects, whereas Cu induced cell shrinkage, impaired motility, and inhibited cell division. The combination treatment (CC) largely reflected Cu-driven morphological and functional changes, with Co coexisting without counteracting Cu’s effects. Taken together, these findings reveal compound-specific mechanisms of action for Cu and Co in OSCC therapy. Full article

Chronic urticaria (CU) is a mast cell-driven inflammatory skin disorder characterized by recurrent wheals, angioedema, or both lasting more than six weeks, often resulting in significant impairment of quality of life. Although CU has traditionally been regarded as a predominantly histamine-mediated condition, evidence accumulated over the past decade has redefined chronic spontaneous urticaria (CSU) as a complex immune-mediated disease with marked biological heterogeneity. Distinct pathogenic mechanisms involving autoimmune pathways, dysregulated mast cell activation, and chronic inflammatory networks have been identified, providing a mechanistic basis for disease persistence, variable severity, and therapeutic refractoriness. This review synthesizes current concepts in CSU pathophysiology, with emphasis on mast cell biology, autoimmune endotypes, and inflammatory amplification mechanisms. We further discuss emerging biomarkers with potential relevance for disease stratification and treatment prediction, as well as established and novel therapeutic strategies targeting key pathogenic pathways. By integrating mechanistic insights with clinical implications, this review highlights the transition toward endotype-driven and biomarker-guided management of chronic urticaria. Full article

The Beni Snassen belt (northeastern Morocco) hosts several Mississippi Valley-type Pb-Zn ± Cu occurrences localized along the Variscan basement/Lower Liassic carbonate interface within the Atlasic foreland system. This study integrates geological observations with organic petrography and C-O-S-Pb isotopic systematics to constrain the origin of mineralizing fluids, metal source, and ore-forming processes within a basin-scale metallogenic system. The host sequence consists of unmetamorphosed, dolomitized Pliensbachian carbonates with marl interbeds and organic-rich black shales. Mineralization is structurally focused along ENE-WSW and E-W faults and occurs as massive calcite-galena veins, “en échelon” tension gashes, vug fillings, and solution-collapse breccias. Ore-stage calcite exhibits restricted isotopic variability (δ¹³C = −4.7 to +1.2‰; δ¹⁸O = 14.9 to 19.7‰), consistent with rock-buffered basinal fluids and extensive fluid–carbonate interaction. Calculated δ¹⁸O_H2O values indicate precipitation from evolved saline brines variably mixed with meteoric waters. Galena δ³⁴S values (−20.9‰ to +10.3‰) reflect thermochemical sulfate reduction (TSR) under fluctuating redox conditions. Pb isotope compositions define a tight linear cluster between upper crust and orogene growth curves, indicating a predominantly upper crustal metal source, notably Triassic dolerite–diabase lithologies, with a possible contribution from organic-rich black shales. High-reflectance pyrobitumen (VR₀ up to 4%) indicates thermal conditions exceeding those predicted by local burial history, supporting long-distance migration of hydrocarbon-bearing metalliferous fluids from overpressured basin compartments, most plausibly the adjacent Neogene Guercif Basin. Fault reactivation during Late Miocene transtension fostered basin-scale fluid focusing and ore deposition. Hence, the Beni Snassen district represents a basin-integrated MVT system involving crustal metal leaching, organic-assisted metal transport, TSR-mediated sulfur reduction, and structurally focused fluid flow. These results refine metallogenic models for the Atlasic belts and highlight the exploration potential of structurally reactivated foreland basins hosting coupled hydrocarbon-hydrothermal systems. Full article

The management of diabetic chronic wounds (DFUs) is challenging due to persistent bacterial colonization, impaired neovascularization, and disordered inflammation. We engineered a multifunctional photothermal hydrogel (PPCS) by integrating CuS nanoparticles and high-concentration sucrose to establish a dual-action therapeutic cascade: potent antibacterial eradication followed by pro-angiogenic stimulation. Upon NIR irradiation, the PPCS system executes a combinatorial anti-infective mechanism: CuS-mediated photothermal effect and ROS generation are amplified by sucrose’s hyperosmotic pressure, achieving 99.3% bacterial eradication. Beyond sterilization, the hydrogel acts as a Cu²⁺ sustained-release depot, significantly promoting HUVEC proliferation and migration. This pro-angiogenic effect is mechanistically linked to the upregulation of HIF-1α/VEGF signaling, accelerating neovascularization. Furthermore, sucrose efficiently manages wound exudate, maintaining a repair-conducive microenvironment. In a diabetic rat model, the PPCS dressing demonstrated superior therapeutic efficacy, achieving an accelerated wound closure rate of 99.4% by Day 14, significantly surpassing the control group’s 78.9%. This work presents a tailored hydrogel platform that effectively targets both persistent infection and impaired vascularization, offering a precise and highly efficient therapeutic modality for the clinical management of diabetic chronic wounds. Full article

This study presents a quantitative investigation of substituent effects on the stability of 1:2 complexes formed between para-substituted 2-phenylbenzimidazole ligands and Cu(II) or Co(II) ions. The ligands, featuring hydroxyl (–OH), chloro (–Cl), and nitro (–NO₂) substituents, were synthesized via copper acetate-mediated oxidative cyclization. Stability constants (log K) were determined spectrophotometrically using both the Benesi–Hildebrand and Job methods, which yielded perfectly consistent results and confirmed ML₂ stoichiometry. For both metal series, the stability decreases in the order –OH > –Cl > –NO₂. Excellent linear correlations were obtained between log K and Hammett σ constants, yielding reaction constants of ρ = −0.79 for Cu(II) and ρ = −1.00 for Co(II). These negative ρ values confirm that electron-donating substituents enhance complex stability by increasing electron density on the donor nitrogen. Furthermore, the stability constants for Cu(II) complexes are approximately two orders of magnitude higher than those for Co(II), in agreement with the Irving–Williams series. This work establishes a clear, predictive structure–stability relationship and validates the combined methodological approach for quantifying metal–ligand interactions in tunable benzimidazole systems. Full article

The long-term accumulation of phosphogypsum (PG) stacks has caused combined pollution of total phosphorus (TP), fluoride (F⁻), metals and metalloids (MMs), posing a severe threat to regional ecological security. To clarify the migration characteristics of pollutants in PG stacks, water leaching experiments and environmental risk assessment were conducted in 21 typical PG stacks in Southwest China. The spatial differentiation and vertical migration characteristics of pollutants under various coverage measures (high-density polyethylene (HDPE) film covering, soil covering, a composite of film–soil covering, and open-air storage) at different pH conditions were systematically analyzed. Results indicated that under open-air stockpiling conditions, the surface accumulation of TP and F⁻ was the most significant among all covering measures, corresponding to the highest environmental risk. In contrast, the membrane–soil composite covering exhibited the optimal inhibitory effect on the surface diffusion of TP and F⁻, but was less effective for metal and metalloid enrichment. Under acidic conditions (pH < 6), the vertical migration capacity of TP, F⁻, and MMs (Cu, Cd, Cr, Pb, and Zn) increased, leading to enrichment in the deep layers of the stack. With the increase in pH, the calcium-mediated precipitation–adsorption effect created a “geochemical barrier”, facilitating the solid-phase fixation of pollutants. A significant positive correlation among pollutants indicates synergistic release and fixation behaviors. In addition, a pH-controlled P-F-MM source-to-sink conceptual model was established, outlining the dissolution, precipitation, adsorption, fixation and re-enrichment pathway from fresh stock to leachate. This work provides insights for optimizing cover designs and pollution control strategies. Full article

In permanently submerged coastal wetlands, interactions between biogeochemical processes and microbial communities strongly influence greenhouse gas (GHG) fluxes. To improve our understanding of how redox-driven processes shape GHG dynamics in these ecosystems, we investigated the relationships among iron (Fe) pools, microbial dynamics, and the potential GHG production in subaqueous soils from an interdunal wetland in San Vitale Park (Italy), permanently submerged and affected by seasonal oscillations of the saline water table. Two subaqueous soil columns (WAS-2 and WAS-4), collected from similar settings, were analyzed. Surface layers of WAS-4 showed higher salinity and carbonate content, whereas WAS-2 was characterized by overall higher Fe concentrations. Distinct vertical distributions of organic matter and sulfur (S) were shown along depth. Laboratory incubations revealed that nitrous oxide (N₂O) production was up to ten times higher in WAS-2 than in WAS-4, with peaks in the top 13–14 cm, consistent with more active nitrification-denitrification in surface layers. Methane (CH₄) and carbon dioxide (CO₂) fluxes decreased with depth, reflecting reduced availability of labile carbon. Methanomicrobiales dominated CH₄-producing layers, indicating hydrogenotrophic methanogenesis, while amoA-carrying Nitrosomonadales and Thaumarchaeota, occurred in shallow, organic-rich layers where ammonia supported nitrification and denitrification. Denitrifiers mainly belonged to α- and β-Proteobacteria, consistent with their direct contribution to N₂O peaks. Spearman’s correlations showed N₂O positively correlated to sulfur and labile carbon (C), supporting denitrification under moderately reducing conditions. CH₄ and CO₂ positively correlated with organic C (Corg), total nitrogen (TN), and reactive Fe forms, reflecting redox-mediated microbial respiration and methanogenesis. Trace elements (B, Cr, Cu, Ni) acted as micronutrients or inhibitors depending on concentration. Canonical correspondence analysis indicated depth-structured links among gas fluxes, soil chemistry (Corg, TN, S/C, CaCO₃, P), and microbial distributions: surface layers, rich in labile C and nutrients, supported active bacteria and archaea involved in decomposition, nitrification, and denitrification, whereas deeper layers hosted oligotrophic archaea adapted to inorganic substrates. Overall, Fe pools appeared to be associated with soil processes relevant to GHG dynamics, although the extent of their regulatory role remains uncertain due to potential alterations of redox-sensitive Fe fractions during sample handling. These results contribute to broader efforts to predict GHG emissions in submerged wetland soils by linking redox stratification, inorganic chemistry, and microbial functional groups. Full article

The mechanical behavior of metallic core–shell nanoparticles is critical for their use as reinforcement particles and additive manufacturing feedstocks, yet their deformation mechanisms remain incompletely understood. This study employs molecular dynamics simulations to investigate the compressive response of a Cu-core/Al-shell nanoparticle and compares it with solid Cu, solid Al, and a hollow Al shell of the same size under uniaxial loading along ⟨100⟩, ⟨110⟩, ⟨111⟩, and ⟨112⟩ directions. The single-material nanoparticles show strong anisotropy: solid Cu exhibits orientation-dependent transitions from dislocation slip to deformation twinning, while introducing a void to form a hollow Al shell reduces stiffness and strength, confines plasticity to the shell wall, and suppresses extended load-bearing twins. The Cu–Al core–shell nanoparticle combines these behaviors in an orientation-dependent manner. Under ⟨110⟩ and ⟨112⟩ loading, deformation is largely shell-dominated, whereas ⟨100⟩ and ⟨111⟩ loading more strongly activates the Cu core. Mechanistically, ⟨100⟩ is characterized by Shockley partial activity and junction/lock formation in the Al shell coupled with twinning in the Cu core; ⟨110⟩ shows primarily shell partials with limited core involvement; ⟨111⟩ promotes partial-dislocation activity in both shell and core; and ⟨112⟩ produces localized, twin-dominated bands in the Al shell with shell-thickness-dependent twin extension into the Cu core. These trends are rationalized using Schmid factor considerations for $\left\{111\right\}⟨110⟩$ slip and $\left\{111\right\}⟨112⟩$ partial/twinning shear, together with the effects of faceted free surfaces and the Cu–Al interface. The core–shell geometry enables two concurrent interface-mediated pathways, i.e., (i) stress transfer and reduced cross-interface transmission and (ii) circumferential bypass within the shell, which together yield only slight flow-stress increases over solid Al while markedly reducing stress serrations compared with both solid Cu and solid Al. Across all orientations, the core–shell structures also exhibit delayed yielding (higher yield strain) relative to solid Cu, indicating enhanced ductility. The results provide an atomistic basis for designing Cu–Al core–shell nanoparticles for robust particle-based processing and additive manufacturing feedstock, and for informing multiscale models with mechanism-resolved, orientation-dependent inputs. Full article

Green-synthesis routes for producing CuO nanoparticles offer a simplified, sustainable, and low-cost replacement for conventional chemical methods, eliminating the need for harsh chemicals and providing an easily scalable process for industrial-level production. Although numerous studies have investigated synthesizing CuO nanoparticles from single plant extracts, comparative assessments of multi-plant-mediated CuO nanoparticles alongside synthetic CuO remain limited. In this work, CuO nanoparticles were green-synthesized from three different plant sources, namely ginger, red onion peels, and garlic, and their physicochemical and biological properties were tested against the synthetic CuO. All plant extracts produced pure-phased monoclinic CuO nanoparticles as confirmed by UV–Vis, XRD, FTIR, and SEM/EDX analyses. SEM showed distinct nanoparticle morphologies, with CuO from ginger extract exhibiting uniform nanocubes, while nanoparticles from red onion and garlic extracts exhibited more aggregated and irregular structures. Their crystallite sizes were 8–9 nm lower than the ~11 nm observed for the synthetic CuO, highlighting the phytochemical role in shaping the nanoparticles’ morphology. The antibacterial efficacy against S. aureus and E. coli showed that ginger-derived and synthetic CuO had the strongest bacterial inhibition and bactericidal potency compared to onion- and garlic-derived CuO samples. However, synthetic CuO had the highest cytotoxicity risk, hindering its suitability for biological uses, while CuO-ginger maintained good cell viability at moderate concentrations. CuO-onion and CuO-garlic gave lower antibacterial cytocompatibility performance due to their thicker capping layers, which led to decreased Cu²⁺ release and ROS production. Ginger-derived CuO achieved an optimal trade-off between antibacterial and cytotoxic efficiency, highlighting its prospects as a candidate for biomedical applications. Full article

The electrochemical interaction between aggressive ions and metals plays a key role in corrosion failure processes. The Langmuir adsorption isotherm equation was employed to reveal that surface coverage remains largely unchanged at higher concentrations, with the concentration effect partially mediated by the dielectric properties of the solution. The work function and adsorption energy of two typical corrosive elements, Cl and S, adsorbed on the surfaces of two metals (Al and Cu) were systematically calculated. By adjusting solubilization parameters in different implicit solvent models, variations in dielectric properties at similar surface coverage under different concentrations were simulated. It was observed that as the solution concentration increased, the electrostatic shielding effect of the surface solution was enhanced, while the changes in adsorption energy were not statistically significant. However, the work function was found to increase by approximately 20–90 meV with increasing concentration, with the magnitude of this increase dependent on the metal type and surface orientation. This enhancement further strengthened the adsorbate–substrate interaction, thereby influencing the electrochemical reaction kinetics of the surface material. Full article