Highly active nanozyme based on nitrogen-doped graphene quantum dots and iron ion nanocomposite for selective colorimetric detection of hydroquinone.

Inspired by the iron porphyrin structure of natural horseradish peroxidase (HRP), an efficient carbon-based nanozyme was fabricated using nitrogen-doped graphene quantum dots (NGQDs) and iron ion (Fe3+) nanocomposite, enabling selective distinguishment of hydroquinone (HQ) from its isomers. NGQDs with good dispersibility and uniform size were synthesized via a one-step hydrothermal process. NGQDs lacked peroxidase-like activity but the formed nanocomposite (Fe3+-NGQDs) upon Fe3+ addition possessed high peroxidase-like activity. Fe3+-NGQDs nanocomposite exhibited shuttle-shaped structure (∼30 nm), the lattice structure of NGQDs and electron transfer between Fe3+ and NGQDs. The Fe3+-NGQDs nanocomposite can catalyze the production of superoxide radicals (•O2-) from H2O2. The Michaelis constant (Km) of Fe3+-NGQDs (0.115 mM) was lower than that of natural HRP (0.434 mM) with 3,3',5,5'-tetramethylbenzidine (TMB) as the substrate and the maximum initial reaction rate (Vmax, 16.47 × 10-8 M/s) was nearly 4 times higher than that of HRP using H2O2 substrate. HQ, unlike its isomers catechol (CC) and resorcinol (RE), could consume •O2- generated from the decomposition of H2O2 catalyzed by Fe3+-NGQDs nanocomposite, reducing the oxidation of TMB. This principle enabled selective colorimetric determination of HQ ranged from 1 µM to 70 µM and a limit of detection (LOD) of 0.2 µM. Successful determination of HQ in pond water was also realized.

Micro-droplet printed ion-selective membrane sensors for in situ monitoring of marine heavy metal ions.

Fast, accurate, and reliable techniques for marine toxic heavy metal ions (HMI) detection are critical for the ecological environment and human health. One of the fatal drawbacks of traditional ion selective electrochemical sensors is that the modification of electrode cannot be accurately quantified, resulting in poor repeatability of the detection electrode and large error between the multi-electrode detection results. In order to tackle this challenge, this study presents ultra-fine micro-droplet printed electrodes for the in-situ detection of Cd2+, a carcinogenic and toxic HMI commonly found in the ocean. The ion selective membrane casting liquid was dispersed into tiny droplets with a diameter of micron through microfluidic technology, and the microdroplets were precisely arranged on the electrode surface. As a result, the modification error of electrode was reduced to pL level (accurate to 10 pL), which greatly improved the repeatability between electrodes prepared in different batches. The results of experiments with pure electrolyte, interference ions and artificial seawater indicated that the micro-droplet printed sensors possessed excellent properties of accuracy, precision, repeatability, and anti-interference. This novel micro-droplet printed sensor has the potential to capture an accurate picture of nearshore HMI in heterogeneous environments under shock conditions.

Efficient hydrogenation of Nitrocyclohexane to cyclohexanone oxime over CuFeAl-Layered Double Hydroxide: The promoting role of FeOx.

Nitrocyclohexane (NCH) hydrogenation to cyclohexanone oxime (CHO) is of great significance in the production of caprolactam. In this work, CuFeAl-Layered Double Hydroxide (CuFeAl-LDH) catalysts with lamellar structure were prepared by co-precipitation method and applied for NCH hydrogenation, and the promoting role of FeOx was discussed. It was found that FeOx species promote the reduction of Cu2+ and control the ratio of Cu+ to Cu0. In situ DRIFT and density-functional theory (DFT) calculation results confirm that the presence of FeOx species can act as lewis base site to reduce the acid sites and facilitate the isomerization of nitrosocyclohexane to CHO, and promotes the adsorption of NCH and the desorption of the formed CHO to prevent its further reaction to form byproducts. CuFe0.05Al shows the best catalytic performance of 100 % NCH conversion and 93.35 % selectivity to CHO under mild conditions. This work provides a new idea for the design of non-noble metal-based catalysts with high activity for the selective hydrogenation of nitro compounds.

Trimetallic Ni-CuCoN0.6 Ohmic junction for the enhanced oxidation of methanol and urea.

Methanol oxidation reaction (MOR) and urea oxidation reaction (UOR) can be utilized as effective alternatives to the anodic oxygen evolution reaction (OER) in overall water-splitting. Nevertheless, the development of cost-effective, highly efficient and durable electrocatalysts for MOR and UOR remains a significant challenge. Herein, the Ohmic junction (Ni-CuCoN0.6@CC) comprising CuCoN0.6 nanosheets and Ni nanoparticles anchored on carbon cloth (CC) was successfully synthesized via a two-step hydrothermal process followed by pyrolysis. The Ni-CuCoN0.6@CC demonstrates exceptional performance in both MOR (1.334 V@10 mA cm-2) and UOR (1.335 V@10 mA cm-2), coupled with outstanding durability, maintaining 88.70 % current density for MOR and 88.92 % for UOR after a rigorous 50-h stability test. Furthermore, the Ni-CuCoN0.6@CC demonstrates a high selectivity for oxidizing methanol to formic acid, achieving Faraday efficiencies exceeding 90 % at various current densities in the context of MOR. The outstanding performance of Ni-CuCoN0.6@CC in terms of MOR and UOR either surpasses or closely approaches the levels reported in previous literature, primarily due to the synergistic effect resulting from the Ohmic junction: in this system, Ni serves as the principal active component, Co augments catalytic activity and diminishes onset potential, while Cu enhances long-term durability. Moreover, CuCoN0.6 nanosheets effectively modulate electronic structure and optimize the morphology of Ni, leading to the exposure of numerous defects that provide a wealth of active sites for the reaction. Additionally, the exceptional hydrophilic and aerophobic surface promotes enhanced mass transfer. Density functional theory (DFT) calculations show that Ni-CuCoN0.6@CC enhances reactant adsorption and product desorption, reducing energy barriers and expediting MOR and UOR kinetics.

Magnetic modulation on chiroptical activities of nematically assembled carbon dots.

Effectively harnessing the assembly of achiral carbon dots into a chiral manner is a prominent step for applying carbon dots into the area of stereoselective optoelectronics and theranostics. Herein, magnetic-modulated and circularly polarized luminescence (CPL)-active photonic thin films were presented in this article via co-assembly and magnetic-mediation strategy of cellulose nanocrystals, carbon dots and magnetic nanoparticles. The photonic bandgap of the composite films is modulated via interfacial interactions between the building blocks, and more efficiently via external magnetic field which can further enhance the selective reflection of the films with a maximum CPL anisotropic factor as high as -0.92, indicating the optimized condition for achieving CPL signals is basically when the photonic bandgap (PBG) are close to the emission peaks of nanocomposite films, which may essentially facilitate the selective reflection effect and leads to the output of opposite CPL signals. Such strategy would inevitably boost the development of carbon dots based chiral devices and reagents into the realm of chirality-related biological issues and next generation chiral optoelectronics.

Molecularly imprinted polymer based on covalent organic framework coated steel substrate as the mass spectrometric ionization source for the direct detect of aflatoxins in complex food matrices.

Ambient mass spectrometry allows direct analysis of various sample types with minimal or no pretreatment. However, due to the influence of matrix effects, there are sensitivity and issues in analyzing trace analytes in complex food samples. In this work, we developed a spray mass spectrometry platform based on SSS@TPBD-TPA@MIPs (Stainless steel substrate (SSS), terephthalaldehyde (TPA), N, N, N', N'-tetrakis(p-aminophenyl)-p-phenylenediamine (TPBD), molecularly imprinted polymer (MIP)), for rapid, in situ, high-throughput, highly enrichment efficiency and highly selective trace analysis of aflatoxins. By simplifying the sample pretreatment and directly applying high voltage for ESI-MS, the analysis can be completed within 1 min. The established method base on SSS@TPBD-TPA@MIPs exhibited high sensitivity and accuracy when determine trace level AFs in maize and peanuts. The results demonstrated a good linear relationship within the range of 0.01-10 µg/L, with the determination coefficient (R2) ≥ 0.9956. The limits of detection (LODs) was 0.035-0.3 ng/mL and limits of quantitation (LOQs) was 0.12-0.99 ng/mL, with acceptable recovery rate of 82.09-115.66 % and good repeatability represented by the relative standard deviation (RSD) less than 17.43 %. Furthermore, SSS@TPBD-TPA@MIPs exhibited excellent reusability, with more than 8 repeated uses, and showed good adsorption performance.

La1-xSrxFeO3-δ Perovskite Oxide Nanoparticles for Low-Temperature Aerobic Oxidation of Isobutane to tert-Butyl Alcohol.

The development of reusable solid catalysts based on naturally abundant metal elements for the liquid-phase selective oxidation of light alkanes under mild conditions to obtain desired oxygenated products, such as alcohols and carbonyl compounds, remains a challenge. In this study, various perovskite oxide nanoparticles were synthesized by a sol-gel method using aspartic acid, and the effects of A- and B-site metal cations on the liquid-phase oxidation of isobutane to tert-butyl alcohol with molecular oxygen as the sole oxidant were investigated. Iron-based perovskite oxides containing Fe4+ such as BaFeO3-δ, SrFeO3-δ, and La1-xSrxFeO3-δ exhibited catalytic performance superior to those of other Fe3+- and Fe2+-based iron oxides and Mn-, Ni-, and Co-based perovskite oxides. The partial substitution of Sr for La in LaFeO3 significantly enhanced the catalytic performance and durability. In particular, the La0.8Sr0.2FeO3-δ catalyst could be recovered by simple filtration and reused several times without an obvious loss of its high catalytic performance, whereas the recovered BaFeO3-δ and SrFeO3-δ catalysts were almost inactive. La0.8Sr0.2FeO3-δ promoted the selective oxidation of isobutane even under mild conditions (60 °C), and the catalytic activity was comparable to that of homogeneous systems, including halogenated metalloporphyrin complexes. On the basis of mechanistic studies, including the effect of Sr substitution in La1-xSrxFeO3-δ on surface redox reactions, the present oxidation proceeds via a radical-mediated oxidation mechanism, and the surface-mixed Fe3+/Fe4+ valence states of La1-xSrxFeO3-δ nanoparticles likely play an important role in promoting C-H activation of isobutane as well as decomposition of tert-butyl hydroperoxide.

Scale-Dependent Growth Modes of Selective Area Grown III-V Nanowires.

Due to their flexible geometry, in-plane selective area grown (SAG) nanowires (NWs) encompass the advantages of vapor-liquid-solid NWs and planar structures. The complex interplay of growth kinetics and NW dimensions provides new pathways for crystal engineering; however, their growth mechanisms remain poorly understood. We analyze the growth mechanisms of GaAs(Sb) and InGaAs/GaAs(Sb) in-plane SAG NWs using molecular beam epitaxy (MBE). While GaAs(Sb) NWs consistently follow a layer-by-layer growth, the InGaAs/GaAs(Sb) growth transitions from step-flow to layer-by-layer and layer-plus-island depending on the InGaAs thickness and the NW dimensions. We extract the diffusion lengths of Ga adatoms along the [11̅0] and [110] directions under As2 during GaAs(Sb) growth. Our results indicate that Sb may inhibit the layer-by-layer to step-flow transition. Our findings show that different growth modes can be achieved in the MBE of in-plane SAG NWs grown on the same substrate and highlight the importance of the interplay with NW dimensions.

Evaluation of the results of closed kinetic chain exercises applied in the conservative treatment of patellofemoral pain syndrome by means of shear wave elastography: A randomized controlled trial.

PURPOSE: Non-selective closed kinetic chain exercises (NSKCE) and or selective closed kinetic chain exercises (SCKCE) has been shown to increase Vastus medialis obliquus (VMO) muscle power in patellofemoral pain syndrome (PFPS). However, the superiority of the exercises to each other has not been shown. This study aimed to evaluating the effects of different exercises on the stiffness of the VMO and vastus lateralis (VL) muscles, pain management, functional scores, and thigh circumferences. METHODS: One hundred 60 knees of 80 patients followed up in our outpatient clinic between December 2016 and February 2018 were included in the study. Patients were divided into two groups as 40 patients with single-sided PFPS (20 male and 20 female patients) and 40 healthy controls (20 male and 20 female patients). The patients in each group were divided into subgroups according to NSCKCE or SCKCE. VMO and VL muscles were measured by shear wave elastography (SWE) before and after a 6-weeks therapy. RESULTS: There was a significant decrease in Visual Analog Scale (VAS) score while a significant increase was found in Lysholm Knee Scale (LKS), however, no statistically difference was found between the two exercise groups in PFPS patients. The effect of both exercises on pain and functional improvement was similar. CONCLUSION: Decrease in VAS scores, increase in LKS scores, increase in thigh circumference measurements, and increase in the stiffness of VMO and VL muscles were observed in both groups who received SCKCE and NSCKCE on PFPS patients. TRIAL REGISTRATION: Study registered at ClinicalTrials.gov (registration number: NCT05427357). DESIGN: Randomized controlled trial.

Mandible Reconstruction With Custom-Made Plates in Medication-Related Osteonecrosis of the Jaw-A Case Series.

Background: Restoration of the mandibular region after segmental resection surgery is crucial for masticatory function and facial aesthetics. The precision of three-dimensional printers has advanced in recent years, enabling the development of fully customized reconstruction plates. In recent years, three-dimensional printing technology has been applied in the field of dental and oral surgery. Among these, the selective laser melting method has been developed. This case report was aimed at exploring the utility in restoring mandibular morphology. Cases: Patients diagnosed with medication-related osteonecrosis of the jaw (MRONJ) in Oral and Maxillofacial Surgery at Kanazawa Medical University Hospital who underwent mandibular disarticulation and immediate completely customized reconstruction plate (COSMOFIX) were included. Case 1 involved a female in her 70s with MRONJ on the right side of the mandible. Case 2 involved a female who received bisphosphonates for extensive metastatic breast cancer, resulting in MRONJ affecting the bilateral mandible. Case 3 involved a woman who developed MRONJ on the right side of the mandible during alendronate treatment for osteoporosis. Completely customized reconstruction plates were used for reconstruction after segmental resections. Findings: The three patients adapted to the remaining bone. The reconstructed and preoperative mandibular morphologies were similar. Conclusions: In conclusion, the use of completely customized reconstruction plates obviates the need for bending and other adaptations, reduces surgical time, and improves postoperative aesthetics. Of significance, preparing completely customized reconstruction plate requires about 3 weeks; thus, careful case selection and scheduling are indispensable.

Medicinal chemistry insights in neuronal nitric oxide synthase inhibitors containing nitrogen heterocyclic compounds: a mini review.

Many scientific reports over the last two decades have focused on the discovery and development of novel nNOS inhibitors. The structural identity of isoforms, bioavailability, pharmacokinetic, and safety profile issues remain major obstacles in the discovery of more potent and selective nNOS inhibitors. This review aims to provide an in-depth overview of the molecular interaction patterns between nNOS active site and inhibitors containing structurally diverse nitrogen heterocyclic compounds and highlight the structural properties needed to develop selective nNOS inhibitors. Previously published data allowed the usage of the structure-driven approach in the designing of selective nNOS inhibitors, which relies on the specific structural features required to achieve isoform-selectivity towards nNOS. The incorporation of chiral pyrrolidine ring, two aminopyridine heads, or a specific amino tail group, along with the inhibitor's capacity to adopt the curled conformation in the nNOS environment significantly strengthens the molecular interaction between the inhibitor and nNOS residues by forming specific electrostatic interactions and non-bonded contacts that are vital for isoform selectivity. Additional structure-activity relationship investigations are necessary to elucidate more structural characteristics that will ultimately resolve the exact structural basis required for isoform-selective inhibition of nNOS.

Insight into the Efficient Selective Reduction of Cr(VI) in Sulfite/UV Process under Near-Neutral Conditions: The Critical Role of In Situ-Generated Sulfite Radical.

Efficient removal of contaminants in complex water matrices under mild conditions is highly desirable but still challenging. In this study, we unraveled the overlooked but crucial role of sulfite radical (SO3·-) in the efficient selective reduction of toxic Cr(VI) under near-neutral conditions. Fast removal of Cr(VI) at around pH 7 in sulfite/UV was found to be attributable to high reactivity of SO3·- toward HCrO4- (∼5.3 × 106 M-1 s-1). Furthermore, SO3·- was fast generated in situ via one-electron oxidation of S(IV) by transient reactive protonated Cr(V) and Cr(IV) intermediates. Therefore, the specific reactivity of SO3·- and its in situ generation together resulted in the surprisingly positive effect of nitrate and the efficient reduction of Cr(VI) in authentic surface water and industrial wastewater. A mathematical model was developed to simulate Cr(VI) removal in the process, and thus quantitatively demonstrated the roles of reactive species, i.e., SO3·- contributed to ∼93% of Cr(VI) reduction in surface water. Overall, this study provides an insight into the pivotal role of SO3·- in Cr(VI) reduction, and underscores its significance in selective reduction and detoxification of contaminants.

Revealing Anion Exchange in Two-Dimensional Nanocrystals.

Ion exchange is a powerful postsynthesis tool for the design of functional nanomaterials. However, achieving anion exchange while maintaining the original morphology and crystal structure, as well as elucidating the mechanism, remains challenging. Here, we developed an anion-exchange strategy under mild conditions and revealed an unusual ion-exchange mechanism in the semiconductor nanoplatelets. Kinetic studies have demonstrated that the transformation follows first-order kinetics, with the ligand restricting the guest anion from diffusing only in one-dimensional directions. By monitoring the reaction process, we demonstrated that the anion exchange reaction occurs selectively on the polar surface of the NPLs and exhibits asymmetry at the two polar end faces. Theoretical simulations further confirmed that anion exchange began from the chalcogenide-dominated facet. The thermodynamic data suggest that guest ions diffuse into the crystal interior via a direct exchange mechanism. This study provides a pathway for anion exchange and the construction of functional nanocrystals and a platform for studying the optoelectronic behavior of single-sheet heterojunctions.

Low Fouling Molecular Selective Channels through Self-assembly of Cross-linked Block Copolymer Micelles for Selective Separation of Dye and Salt.

We report the solvent-evaporation and ionic cross-linking mediated self-assembly of the shell cross-linked micelles of the amphiphilic triblock copolymer containing middle poly(methyl methacrylate) block (hydrophobic) and poly(2-dimethylamino)ethyl methacrylate end blocks (hydrophilic) on the membrane substrate to create molecular selective channels. The formation of selective channels on the substrate is attributed to the local increase of micelle concentration upon solvent evaporation, which leads to the core-core hydrophobic interaction. The post-ionic cross-linking of the shell part further reduces the intermicelle distance, thereby creating interstices for selective separation. The TUF-1:1 membrane prepared by the self-assembly of the cross-linked micelles (triblock copolymer:halide-terminated PEG-based = 1:1 w w-1) and by the post-ionic cross-linking shows molecular weight cutoff of 3000 g mol-1 and pure water permeance of 52 L m-2 h-1 bar-1. The membrane shows 99.5-99.9% rejection of Congo red and Direct red-80 in the presence or absence of salts and Na2SO4 to dye separation factor of about 900. The added functionality (PEG) in the micelle structure provides good fouling-resistant properties toward dye and bovine serum albumin. This work provides the membrane formation mechanism and the advantages of the membrane for fractionation and resource recovery applications.

Cold plasma irradiation of chitosan: A straight pathway to selective antitumor therapy.

Plasma-activated chitosan (PAC) colloids for cancer treatment were obtained by using the cold atmospheric plasma technique. Chitosan solutions were irradiated by plasma ignited in argon gas and in a mixture of argon with nitrogen and oxygen gases in certain ratios. The structural modifications of chitosan and the chemical species generated in plasma were investigated by EPR, LC-MS/MS, XRD, DLS, and TGA methods. The cell viability test showed a selective cytotoxic effect on human breast carcinoma cells (MCF-7), while the human mammary epithelial cells (MCF-10A) were left unharmed. The cytotoxic effect was attributed mainly to chitooligosaccharides, but also to a synergistic effect with other compounds generated in very low concentrations in plasma, such as glyceric acid, ethyl acetate, or tricarballylic acid. The plasma irradiation improved the antioxidant activity and mucoadhesivity, while not affecting the hemocompatibility investigated by a standard hemolysis ex vivo test on mice blood. Moreover, the in vivo biocompatibility investigation at intraperitoneal administration of PAC in mice showed no statistically significant changes in the hematologic, biochemical, and immune system parameters, and no morphologic alterations of the liver and kidney. All these data indicate the cold plasma activation of chitosan as a straight method to produce biocompatible, antitumor systems.

Quasi-modified-Newton method-based selective harmonic elimination in cascaded H bridge inverters.

Multilevel converters have gained significant popularity in medium-voltage and high-power applications due to their numerous advantages over traditional two-level converters. These advantages include reduced harmonic distortion, improved efficiency, and lower stress on power semiconductors. Selective harmonic elimination (SHE) is a modulation method that can be employed with multilevel converters to achieve high-quality output voltage waveforms. In this work, an extension of Broyden's method, known as the Quasi-Modified Newton Method, is implemented for selective harmonic elimination and accurate calculation of switching angles for a wide range of modulation indices. The proposed method is applied to cascaded H bridge inverters operating at levels 5, 7, and 9. The method offers simplicity, reduced computational burden, and faster convergence, making it easily implementable, reducing total harmonic distortion (THD), and reducing RMSE and MAD errors. The paper includes simulation and experimental results that validate the accuracy and effectiveness of the proposed approach.

Does selective root canal retreatment preserve the tooth's fracture resistance? An ex-vivo study.

OBJECTIVES: To assess the tooth's fracture resistance when submitted to a selective root canal retreatment compared to the conventional approach. METHODS: 33 intact permanent mandibular first molars were selected according to specific criteria. After teeth mounting, the primary root canal treatment was conducted and followed by thermo-mechanical aging procedures to mimic a few clinical conditions. The specimens were randomly divided into three groups (n = 11); a control group in which intact teeth were used and two experimental groups according to the retreatment approach: conventional non-surgical retreatment (Conventional-NSR), and selective non-surgical retreatment (Selective-NSR). Later, the teeth were submitted to a final thermo-mechanical aging procedure and tested regarding their fracture resistance (static fracture test). The maximum load to fracture was recorded as were the types of failure modes (repairable or non-repairable fracture). A proper statistical analysis was conducted, considering a significance level of 5%. RESULTS: The Conventional-NSR group showed a mean failure load of 867.7 ± 108.9 N while the Selective-NSR group had 1106.8 ± 159.8 N (P = 0.012). Both retreatment groups showed significantly lower results when compared to the control group. Additionally, the Conventional-NSR group showed higher proportions of non-repairable fractures (54.5%) when compared to both the Selective-NSR (36.4%) and control (18.2%) groups. CONCLUSIONS: Selective root canal retreatment preserved the tooth's fracture resistance compared to the conventional retreatment approach. CLINICAL TRIAL NUMBER: Non-applicable. Conducting the current experiment was limited to obtaining approval from the local Research Ethics Committee at the Faculty of Dentistry, Minia University (Committee No. 105, Registration No. 902, Date: 26/3/2024).

Selective adsorption of arsenic by water treatment residuals cross-linked chitosan in co-existing oxyanions competition system.

Selective adsorption of arsenic in co-existing oxyanions competition systems remains a significant challenge in water treatment due to the limitations of adsorbent materials that often overlook competitive adsorption, resulting in an overestimation of their actual purification potential for target contaminants. In this study, a novel hydrogel bead adsorbent, composed of water treatment residuals (WTRs) and chitosan (Chi), was developed to selectively remove arsenic, while minimizing the interference from phosphate, which is the strongest and most representative competitor in multi-oxyanion systems. The WTRs-Chi beads (WCB) adsorbents were optimized by adjusting the ratios of WTRs:Chi, with characterization results indicating that increased WTR doping improved the degree of crosslinking and the formation of bidentate complexes with enhanced electrostatic selectivity. Importantly, the co-existence of phosphate had minimal adverse effects on arsenic removal compared to other reported adsorbents. The maximum adsorption capacity for As (V) in the binary system was 34.12 mg/g, and the adsorption behavior was fitted well by the pseudo-second-order kinetic model and the extended Langmuir isotherm model. The experimental results, supported by X-ray photoelectron spectroscopy analysis (XPS), revealed that both As (V) and P (V) adsorption in the single system were driven by electrostatic attraction and ligand exchange. However, in the binary system, the inhibition of P (V) adsorption was attributed to competitive desorption caused by electrostatic repulsion, which hindered the formation of inner-sphere complexes. This study provides a practical approach for developing selective adsorbents to address arsenic contamination in complex water environments and promotes the recycling of municipal solid waste.

Determinant genetic markers of semen quality in livestock.

The reproductive efficiency of livestock is crucial for agricultural productivity and economic sustainability. One critical factor in successful fertilization and the viability of offspring is the quality of semen. Poor semen quality, especially in frozen-thawed semen used in artificial insemination (AI) have been shown to influence conception outcomes, resulting a negative impact on livestock production. Recent advancements in genetic research have identified specific markers linked to semen quality traits in various livestock species, such as cattle, sheep, goats, pigs, buffalo, and equines. These genetic markers are essential in screening males for breeding suitability, which in turn enhances selective breeding programs. Understanding these markers is crucial for improving reproductive performance and increasing productivity in livestock populations. This review offers a comprehensive overview of the genetic markers associated with semen quality in key livestock. It explores the underlying genetic mechanisms and their practical implications in animal breeding and management. The review underscores the importance of integrating genetic insights into breeding strategies to optimize reproductive efficiency and ensure the sustainable development of livestock industries.

Autophagy: A New Avenue and Biochemical Mechanisms to Mitigate the Climate Change.

Autophagy is a preserved process in eukaryotes that allows large material degeneration and nutrient recovery via vacuoles or lysosomes in cytoplasm. Autophagy starts from the moment of induction during the formation of a phagophore. Degradation may occur in the autophagosomes even without fusion with lysosome or vacuole, particularly in microautophagosomes. This process is arbitrated by the conserved machinery of basic autophagy-related genes (ATGs). In selective autophagy, specific materials are recruited by autophagosomes via receptors. Selective autophagy targets a vast variety of cellular components for degradation, i.e., old or damaged organelles, aggregates, and inactive or misfolded proteins. In optimal conditions, autophagy in plants ensures cellular homeostasis, proper plant growth, and fitness. Moreover, autophagy is essential during stress responses in plants and aids in survival of plants. Several biotic and abiotic stresses, i.e., pathogen infection, nutrient deficiency, plant senescence, heat stress, drought, osmotic stress, and hypoxia induce autophagy in plants. Cell death is not a stress, which induces autophagy but in contrast, sometimes it is a consequence of autophagy. In this way, autophagy plays a vital role in plant survival during harsh environmental conditions by maintaining nutrient concentration through elimination of useless cellular components. This review discussed the recent advances regarding regulatory functions of autophagy under normal and stressful conditions in plants and suggests future prospects in mitigating climate change. Autophagy in plants offers a viable way to increase plant resilience to climate change by increasing stress tolerance and nutrient usage efficiency.