Salinity stress is one of the most detrimental abiotic factors affecting plant development, harming vast swaths of agricultural land worldwide. Silicon is one element that is obviously crucial for the production and health of plants. With the advent of nanotechnology in agricultural sciences, the application of silicon oxide nanoparticles (SiO-NPs) presents a viable strategy to enhance sustainable crop production. The aim of this study was to assess the beneficial effects of SiO-NPs on the morpho-physio-biochemical parameters of rice (Oryza sativa L., variety: DRR Dhan 73) under both normal and saline conditions. To create salt stress during transplanting, 50 mM NaCl was injected through the soil. 200 mM SiO-NPs were sprayed on the leaves 25 days after sowing (DAS). It was evident that salt stress significantly hindered rice growth because of the reductions in shot length (41 %), root length (38 %), shot fresh mass (40 %), root fresh mass (47 %), shoot dry mass (48 %), and root dry mass (39 %), when compared to controls. Together with this growth inhibition, elevated oxidative stress markers including a 78 % increase in malondialdehyde (MDA) and a 67 % increase in hydrogen peroxide (H2O2) indicating enhanced lipid peroxidation were noted. Increasing the chlorophyll content (14 %), photosynthetic rate (11 %), protein levels, total free amino acids (TFAA; 13 %), and total soluble sugars (TSS; 11 %), all help to boost nitrogen (N; 16 %), phosphorous (P; 14 %), potassium (K; 12 %), and vital nutrients. The adverse effects of salt stress were significantly reduced by exogenous application of SiO-NPs. Additionally; SiO-NPs dramatically raised the activity of important antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POX), and catalase (CAT), improving the plant's ability to scavenge reactive oxygen species (ROS) and thereby lowering oxidative damage brought on by salt. This study highlights SiO-NPs' potential to develop sustainable farming practices and provides significant new insights into how they enhance plant resilience to salinity, particularly in salt-affected regions worldwide.

Emerging contaminants and climate change are major challenges that soil organisms are facing today. Triclosan (TCS), an antibacterial agent, is widespread and hazardous in terrestrial environments, but there is a lack of information on how its toxicity will change because of climate change. The aim of the study was to evaluate the short-term effects of increased temperature, decreased soil moisture content (drought), and their complex interaction on triclosan-induced biochemical changes in Eisenia fetida (as well as growth and survival). Four different treatments were used in TCS-contaminated soil tests with E. fetida (10-750 mg TCS kg-1): C (21 degrees C + 60 % water holding capacity (WHC)), D (21 degrees C and 30 % WHC), T (25 degrees C + 60 % WHC), and T + D (25 degrees C + 30 % WHC). The more prominent TCS effect on the survival was seen only after two weeks and at the high TCS concentrations, though a negative effect on weight growth was recorded after one week of exposure at all tested TCS concentrations and climate conditions. Under standard (C) conditions, an activated E. fetida antioxidative system effectively reduced the oxidative stress induced by TCS. Changes in the climatic conditions influenced E. fetid a's biochemical response to TCS-induced oxidative stress. Despite the enhanced activity of antioxidant enzymes, the combination of drought (D) and TCS caused significant lipid peroxidation in E. fetida. Under elevated temperature, E. fetida experienced oxidative stress and a considerable rise in lipid peroxidation due to insufficient activation or inhibition of antioxidant enzymes.

Excessive fluorine accumulation poses a significant threat to soil ecology and even human health, yet its impact on soil fauna, especially earthworms, remains poorly understood. This study employed multi-omics and biomarkers to investigate high fluorine-induced biochemical changes that cause tissue damages in Eisenia fetida. The results demonstrated that earthworms exhibited obvious damage with fluorine addition exceeding 200 mg kg(-1), with stress levels escalating as fluorine contents increased. Further analysis of the underlying mechanisms revealed that fluorine could upregulate genes encoding mitochondrial respiratory chain complexes I-III and downregulate those for IV-V, leading to reactive oxygen species (ROS) accumulation despite antioxidant system activation. The resulting ROS interfered with deoxyribonucleoside triphosphate synthesis, prompting homologous recombination as the main DNA repair mechanism. Additionally, fluorine-induced ROS also attacked and disrupted protein and lipid related metabolisms ultimately causing oxidative damages. These cumulative oxidative damages from high fluorine contents subsequently triggered autophagy or apoptosis, resulting in tissue ulceration and epithelial exfoliation. Therefore, high fluorine could threaten earthworms by inducing ROS accumulation and subsequent biomolecule damages.

Due to the unregulated handling of e-waste, the co-existence of PBDEs and heavy metals in water bodies and soil has been detected with high frequency. However, the combined toxicity for aquatic creatures remains unclear. This study investigated the single and combined stress of BDE3 and copper on the photosynthesis and antioxidant enzyme system of Salvinia natans (L.). The results indicated that there were no negative effects on photosynthetic pigments under single stress of BDE3 or combined stress with copper. However, to deal with oxidative stress, antioxidant defense enzymes, including SOD and CAT, were activated in S. natans. SOD was sensitive in the first stage, while CAT activity was significantly increased until the end of 14 days of incubation. Malondialdehyde content increased significantly, which indicated that excessive reactive oxygen species from pollution of BDE3 or coexistence with copper could not be eliminated. BDE3 concentration in the aqueous phase declined with time, while copper was accumulated over time in S. natans, with BCF increasing to 0.31 +/- 0.073 at the end. Our study indicated that the co-existence of copper could exacerbate the damage caused by BDE3 to S. natans in aqueous environment.

Plastic pollution is a universal problem, and microbial management of plastic waste represents a promising area of biotechnological research. This study investigated the ability of bacterial strains which were isolated from landfill soil to degrade Low-Density Polyethylene (LDPE). Strains obtained via serial dilution were screened for LDPE degradation on Minimal Essential Medium (MEM) with hexadecane. Nine isolates producing clearance zones on hexadecane-supplemented MEM were further tested for biofilm formation on LDPE sheets. High cell surface hydrophobicity isolates (>10%) were selected for detailed biodegradation studies. The C-8 bacterial isolate showed the highest LDPE weight loss (3.57%) and exhibited maximum laccase (0.0219 U/mL) and lipase activity (19 mm) among all bacterial isolates after 30 days. Weight loss was further validated by FTIR and SEM analysis. FTIR analysis revealed that in comparison to control, changes in peak were observed at 719 cm-1 (C-H bending), 875.67 cm-1 (C-C vibrations), 1307.07 cm-1 (C-O stretching), 1464.21 cm-1 (C-H bending), 2000-1650 cm-1 (C-H bending), 2849.85 cm-1 (C-H stretching) in microbial treated LDPE sheets. The treated LDPE also displayed increase in carbonyl index (upto 2.5 to 3 folds), double bond index (1 to 2-fold) and internal double bond index (2 to 2.5-fold) indicating oxidation and chain scission in the LDPE backbone. SEM analysis showed substantial micrometric surface damage on the LDPE film, with visible cracks and grooves. Using 16S rRNA gene sequencing, the C-8, C-11, C-15 and C-19 isolate were identified as Bacillus paramycoides, Micrococcus luteus, Bacillus siamensis and Lysinibacillus capsica, respectively.

The global escalation of soil salinization has led to increased water erosion, adversely impacting plant growth and development. Heat shock proteins (HSPs) are highly conserved proteins found across a wide range of organisms. When biological organisms are stimulated by the external environment, they will express themselves in large quantities. HSPs play a pivotal role in mediating plant responses to abiotic stress. This study identified 22 members of the PcHsp20 gene family with complete open reading frames (ORFs) through transcriptomic analysis conducted under Pugionium cornutum salt stress, and evaluated their expression levels. Notably, PcHsp18.1 was significantly upregulated in the leaves of Pugionium cornutum (L.) Gaertn. Based on this, we cloned the PcHsp18.1 gene and determined through subcellular localization that PcHsp18.1 is localized in both the cytoplasm and nuclear membrane. Subsequently, we transformed the PcHsp18.1 gene into Arabidopsis thaliana to investigate its involvement in the response to salt stress. The results indicated that the overexpressing (OE) plants exhibited improved growth conditions, higher seed germination rates, increased root lengths, a greater number of lateral roots, reduced relative conductivity, and elevated relative chlorophyll content compared to the wild-type (WT) plants. These findings suggesting that the transgenic line possesses enhanced salt tolerance. Moreover, the concentrations of malondialdehyde (MDA) and relative conductivity in the overexpressing (OE) plants were significantly lower than those observed in the wild-type (WT) plants, suggesting a reduced extent of damage to their cell membranes. In comparison to the wild type (WT), the transgenic line (OE) exhibited elevated activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), along with increased proline content, suggesting that the transgenic plants possess enhanced resistance to abiotic stress and a greater capacity for scavenging reactive oxygen species (ROS). Meanwhile, salt treatment resulted in the significant expression of stress-related genes in the transgenic plants. These results indicate that PcHsp18.1 positively regulates salt stress in Arabidopsis.

Fusarium graminearum poses a major threat to barley production worldwide. While seed priming is a promising strategy to enhance plant defense, the use of unconventional priming agents remains underexplored. This study investigates the protective effects of pre-infection camel urine seed priming on barley seedlings challenged with Fusarium graminearum, focusing on growth, disease resistance, oxidative stress, and defense-related responses. Barley grains were primed with camel urine and grown in both Fusarium-infested and uninfested soils. Fusarium infection initially triggered a sharp increase in oxidative stress markers reflecting an early oxidative burst commonly associated with defense signaling. However, in hydro-primed seedlings, this response persisted, leading to sustained oxidative damage and growth suppression. In contrast, camel urine priming modulated the oxidative burst effectively, initially permitting H2O2 accumulation for defense activation, followed by a rapid decline, resulting in an 84.53 % reduction in disease severity and maintenance of seedling growth under infection. This was accompanied by enhanced antioxidant defenses, as indicated by significantly increased activities of antioxidant enzymes, and a 145 % increase in total antioxidant capacity compared to control. Camel urine priming also showed a reduction in shikimic acid levels under infection, suggesting increased metabolic flux toward the phenylpropanoid pathway. Thus, phenylalanine ammonia-lyase activity, phenolic compounds, and flavonoids were significantly elevated. Antifungal enzymes, beta-glucanase and chitinase, also remained high in camel urine-primed seedlings, in contrast to their sharp decline in hydro-primed controls. These findings highlight camel urine priming as a promising, sustainable approach for managing Fusarium in barley.

Recycled aggregates (RA) from construction and demolition waste have many shortcomings such as high porosity and low strength due to adhered mortar and defects inside. If the defects (micropores and microcracks) of RA were repaired, the quality of RA could be improved greatly and its application could be further enlarged. Our previous study has proposed a new modification method, enzyme-induced carbonate precipitation (EICP), to repair the internal defects of RA. In this study, the efforts were focused on the optimization of the EICP treatment. It was found that the two-step immersion method, consisting of preimmersing in CO(NH2)2-Ca(NO3)2 solution for 24 h, then adding urease solution at once with single treatment duration of 5 days and cycling two treatments, was the optimal treatment. Compared with the untreated RA, the water absorption and crush value of treated recycled concrete aggregates (T-CA) were decreased by 7.01% and 9.91%, respectively, and 21.59% and 14.40% for treated recycled mixed aggregates (T-MA), respectively. By use of the optimized EICP-treated RA, the compressive strength of concrete increased by 6.05% (T-CA concrete) and 9.23% (T-MA concrete), and the water absorption of concrete decrease by 11.46% (T-CA concrete) and 18.62% (T-MA concrete). This indicates that the optimized EICP treatment could reduce the porosity and improve the strength of aggregates, thus enhancing the mechanical properties and impermeability of recycled concrete.

Inappropriate fertilization and poor management practices in citrus orchards can cause soil acidification, which may result in potential proton (H+) toxicity to citrus roots. It has been reported that boron (B) can mediate H+ detoxification in citrus; however, the mechanisms remain limited. Herein, a hydroponic experiment was employed to unravel the alleviation mechanism of B on H+ toxicity at pH 4 in trifoliate (Poncirus trifoliate (L.) Raf.) seedlings. H+ toxicity reduced cytoplasmic pH from 7.2 (control) to 6.9 and vacuolar pH from 5.6 (control) to 5.4. This severely damaged the plasma membrane (PM) and inhibited root activity by 35%. However, B supplementation restored cytoplasmic pH to 7.1 and vacuolar pH to 5.6, enhancing root activity by 52% and reducing membrane permeability (relative conductivity decreased by 28%). Mechanistically, B upregulated phosphorylated-type adenosine triphosphatase activity by 14%; conversely, it suppressed vacuolar-type adenosine triphosphatase hyperactivity by 9% to stabilize vacuolar pH. Furthermore, B restored PM integrity by increasing phospholipid (40%), glycolipid (50%) and sulfhydryl group (28%) content, critical for membrane structure and function. It is concluded that B can alleviate root growth inhibition induced by H+ toxicity via increasing the content of key components of PM, which not only repairs the damaged PM but also maintains cellular pH homeostasis through enzyme regulation. The improvement of citrus growth correspondingly safeguards the production capacity.

Soil nitrogen-hydrolyzing enzymes catalyzes a key rate-limiting step in regulating the circulation of soil nutrient elements. The response of soil nitrogen (N)-hydrolyzing enzyme activities to environmental changes has been investigated in different geographic scales or ecosystems. Global warming has increased the frequency of soil freeze-thaw (FT) events, resulting in drastic changes in soil enzyme activities. Clarifying the changes in soil N-hydrolyzing enzymes under freeze-thaw conditions is essential for improving the N cycling and utilization efficiency in soil. However, how soil N-hydrolyzing enzymes respond to FT remains unclear. This study was aimed to analyze the influence of FT on soil N-hydrolyzing enzyme activity in Mollisols. The results showed that soil physicochemical properties and enzyme activities were changed after freeze-thaw events, and freeze-thaw temperature (FTF) had a greater impact on these properties than the number of freeze-thaw cycles (FTC). Correlation analysis showed that total organic carbon (TOC), total nitrogen (TN), total phosphorus (TP) and pH were the major factors affecting enzyme activities in FT events. Soil N-hydrolyzing enzyme activity was mainly regulated by environmental factors, which can directly and indirectly affect the soil enzyme activity. In the soil ecosystem, pH, TOC, TN and TP were important factors in counteracting damage to enzyme activity from FT effects and a suitable environment and adequate nutrients can limit damage to enzymes from FT events. The findings will better predictions the changing patterns of climate change on soil N-hydrolyzing enzyme activity.