It was investigated the potential of Rhodococcus erythropolis AW3 as a biosorbent for the removal of crystal violet (CV) dye from natural water and real effluents. The biosorbent was characterized by flow cytometry, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy X-ray dispersive spectroscopy (EDS), and point of zero charge (pHZPC). Batch biosorption experiments were performed to optimize different parameters involved in the biosorption process. The equilibrium was reached at 90 min at the optimum biosorbent dose of 0.50 g L⁻¹ and pH of 9.0. Results indicated that Langmuir isotherm model was the most suitable to represent the experimental data, and the highest biosorption capacity was 289.8 mg g⁻¹. Kinetic data were well fitted with the pseudo-second-order model. The thermodynamic study showed that the process was favorable, exothermic, and associated with an increase of entropy. Finally, it was demonstrated that the biosorption process using Rhodococcus erythropolis AW3 could be successfully applied to remove CV from natural water and effluents derived from clinical and industrial activities.

In pastures, the application of limestone is often performed after removal of the animals for proper development and establishment of regrowth. Together with this practice, the use of picloram in high concentrations for dicotyledonous weeds is common. Therefore, the evaluation of the behavior of this herbicide in these conditions is critical. The objective of this study was to determine the leaching of the picloram, in the soil with different pH and cultivated with Urochloa brizantha (signalgrass) trimmed or not. The experiment was plotted in a subdivided plot with four repetitions, where the plots were constituted by factors pH (5.3 and 6.4) and Urochloa brizantha managements (trimmed and no trimmed). The subplots were composed by depths (0 to 50 cm). The picloram was applied to the top of the columns after 65 days after emergency. A rain of intensity of 60 mm was simulated 12 h after the herbicide application. Picloram concentration was quantified by the high-performance liquid chromatography. Besides that, a control treatment was added without the presence of the signalgrass, for each substrate. The picloram was not detected in the percolated water through the columns. Picloram leached to deeper layers in the soil with pH 6.4, independently of the signalgrass management. The signalgrass reduced the leaching of the picloram, and those no-trimmed demonstrate a higher capacity to retain the herbicide in superficial layers. The liming of the soil increases the pH and reduces the amount of organic matter in the soil, which favors the leaching of picloram to the layer of 30–35 cm. Trimming of Urochloa brizantha reduces the capacity of this forage to reduce the leaching of picloram.

Despite the widespread use of the insecticide imidacloprid (IMI), a neonicotinoid, there is an urgent need for documenting information related to its acute toxicity. Therefore, this study aims to explore the markers of IMI acute toxicity in the testes of the red palm weevil (Rhynchophorus ferrugineus). The LC₅₀ of IMI was determined at 15.7 ppm for male R. ferrugineus. We assessed biochemical alterations in the testes resulting from treatment with four IMI concentrations (10, 15, 20, and 30 ppm). A reduction in glutathione content and acetylcholine esterase activity followed the IMI concentration in a dependent manner. Catalase activity was inhibited only at 20 ppm, while it increased significantly at 30 ppm. Lipid peroxidation increased steadily as the IMI concentrations increased. Based on ultrastructural analyses of spermiogenic stages, acute IMI toxicity produced swelling and degeneration of spermatid mitochondria indicating structural imbalances in their membranes. Further, abnormal chromatin condensation in nuclei and even loss of sperm were also apparent. This study provides biochemical and ultrastructural indicators for acute toxicity resulting from IMI.

This study enabled the assessment of indoor CO₂ levels and evaluated the relationship between occupancy numbers with CO₂ levels in a Taiwan hospital. The measurements were conducted over four seasons for five working days (Monday to Friday), with sampling conducted simultaneously from 09:00 am to 5:00 pm and across six locations (for spatial variability): hall (H), registration and cashier (RC), waiting area (WA), occupational therapy room (OT), physical therapy room (PT), and outdoors (O). Based on the analysis, three of the five indoor sampling sites showed significant differences in seasonal CO₂ concentrations (p < 0.0001). Based on our result, the physical therapy room had the highest level of CO₂ concentration that exceeded the IAQ standard in Taiwan Environmental Protection Agency (EPA) in all seasons, in that the number of occupants contributing to nearly 40% of the variation in CO₂ measured. Our results also showed that the indoor/outdoor (I/O) ratios of CO₂ concentration for all locations and seasons exceeded 1 in ~ 100% of those locations. The median I/O ratio at sites WA and OT was 2.37 and 2.08 during four seasons, respectively. The highest median I/O ratio was found at site PT, with a calculated range of 2.69 in spring to 3.90 in fall. The highest correlation of occupancy number and CO₂ concentration also occurred in PT which correlation coefficients were estimated at 0.47, 0.65, 0.63, and 0.40 in spring, summer, fall, and winter. The findings of the present study can be used to understand occupancy number and its effect on CO₂ levels in a hospital environment, as well as the effect of time of day (Monday to Friday) on the number of patients admitted.

High-surface-area activated carbons were prepared from an agroindustrial residue, Bertholletia excelsa capsules known as capsules of Para cashew (CCP), that were utilized for removing amoxicillin from aqueous effluents. The activated carbons were prepared with the proportion of CCP:ZnCl₂ 1:1, and this mixture was pyrolyzed at 600 (CCP-600) and 700 °C (CCP700). The CCP.600 and CCP.700 were characterized by CHN/O elemental analysis, the hydrophobic/hydrophilic ratio, FTIR, TGA, Boehm titration, total pore volume, and surface area. These analyses show that the adsorbents have different polar groups, which confers a hydrophilic surface. The adsorbents presented surface area and total pore volume of 1457 m² g⁻¹ and 0.275 cm³ g⁻¹ (CCP.600) and 1419 m² g⁻¹ and 0.285 cm³ g⁻¹ (CCP.700). The chemical and physical properties of the adsorbents were very close, indicating that the pyrolysis temperature of 600 and 700 °C does not bring relevant differences in the physical and chemical properties of these adsorbents. The adsorption data of kinetics and equilibrium were successfully adjusted to Avrami fractional-order and Liu isotherm model. The use of the adsorbents for treatment of simulated hospital effluents, containing different organic and inorganic compounds, showed excellent removals (up to 98.04% for CCP.600 and 98.60% CCP.700). Graphical abstract

Nanofiltration polyamide membranes naturally tend towards biofouling, due to their surface physicochemistries. Nisin, a type of short cationic amphiphilic peptide with antimicrobial properties, has been recognized as a safe antimicrobial for food biopreservation and biomedical applications. This study investigates the impact of nisin on the initial bacterial attachment to membranes, its anti-biofouling properties, and characterizes a non-monotonic correlation between nisin concentration and biofilm inhibition. Nisin was found to inhibit B. subtilis (G+) and P. aeruginosa (G−) attachment to both the nanofiltration membrane and the PES membrane. To determine the mechanism of action, we investigated the polysaccharides, protein, and eDNA as target components. We found that the quantities of polysaccharides and eDNA were significantly changed, resulting in bacterial death and anti-adhesion to membrane. However, there were no discernable impacts on protein. We postulated that nisin could prevent irreversible biofouling by decreasing adhesion, killing bacteria, and reducing biofilm formation. We examined membrane flux behavior through bench-scale cross-flow experiments at a set concentration of nisin (100 μg mL⁻¹), with membrane behavior being confirmed using CLSM images. Results showed that nisin could enhance anti-biofouling properties through both anti-adhesive and anti-bacterial effects, and therefore could be a novel strategy against biofouling of membranes.

In this study, the impact of the curing temperature on leaching behaviour and durability of GGBS-MgO-CaO (GMC)-stabilized/GMC-solidified Pb/Zn-contaminated clay soils was investigated. Toxicity characteristic leaching procedure (TCLP) test, wetting-drying cycles, freeze-thaw cycles and unconfined compression strength (UCS) test were carried out. The influence of curing temperature, binder dosage and curing time on the performance of these samples was investigated. The results show that the leachability and the durability of all samples were improved by increasing curing temperature, curing time and binder dosage. GMCs are more functional in immobilizing Pb compared with Zn, especially in immobilizing high Pb–contaminated soils. The mass loss and Pb/Zn leachability of all samples increased, while their strength decreased after cyclic wetting-drying and cyclic freeze-thaw. Furthermore, curing at 21 °C and 45 °C, the freeze-thaw resistance of 10% GMC-treated soil (GMC10) was found better than that of 10% Portland cement–treated soil (PC10). After 10 cycles of wetting-drying, GMC10 is more chemically stable than PC10.

Copper (Cu) and cadmium (Cd) are ordinary heavy metals. Unreasonable development and utilization of these heavy metals will cause severe pollution to the soils and consequently bring damage to human health. Therefore, recovering soils polluted by heavy metals is crucial. An indoor pot experiment was carried out involving seven treatments, namely, low-concentration Cu stress (Cu1), high-concentration Cu stress (Cu2), low-concentration Cd stress (Cd1), high-concentration Cd stress (Cd2), low-concentration Cu–Cd combined stress (Cu1Cd1), and high-concentration Cu–Cd combined stress (Cu2Cd2), and an uncontaminated soil as a control. Results demonstrated that the net photosynthetic rate and chlorophyll content are approximately 8.36–72.51% and 7.22–36.50%, respectively, lower under the Cu, Cd, and Cu–Cd combined stresses than under the control. The net photosynthetic rates are higher under Cu2 and Cd2 than under Cu1 and Cd1; by contrast, the net photosynthetic rate of leaves is lower under Cu2Cd2 than under Cu1Cd1. The net photosynthesis rate of Cinnamomum camphora is significantly positively correlated with superoxide dismutase activity but is significantly negatively correlated with the total chlorophyll, malondialdehyde, soluble sugar, and proline contents. Young Cinnamomum camphora grows well under Cu, Cd, and Cu–Cd combined stresses and is applicable in ecologically restoring heavy metal–contaminated soils.

The aim of this study was to investigate the effect of autochthonous microorganisms present in soil collected from heavy metal (HM) uncontaminated (Pb ≈ 59 mg kg⁻¹, Cd ≈ 0.4 mg kg⁻¹, Zn ≈ 191 mg kg⁻¹), moderately (Pb ≈ 343 mg kg⁻¹, Cd ≈ 12 mg kg⁻¹, Zn ≈ 1876 mg kg⁻¹), and highly (Pb ≈ 1586 mg kg⁻¹, Cd ≈ 57 mg kg⁻¹, Zn ≈ 3280 mg kg⁻¹) contaminated sites on Zea mays elemental composition, physiological status, and growth parameters. For this purpose, half of the collected soil was sterilized and soil characterization was performed. After 45 days of cultivation, the presence of HM in the soil negatively affected photosynthesis and transpiration rates, relative chlorophyll content, anthocyanins index, chlorophyll fluorescence parameters, and content of oxidative stress products (H₂O₂ and Malondialdehyde) of Zea mays, while soil sterilization had a positive effect on those parameters. Average percentage of colonization of root segments by arbuscular mycorrhiza fungi decreased with an increase of HM contamination in the soil. The increase in shoot concentration of HMs, particularly Cd and Zn, was a result of contaminated soils sterilization. Aboveground biomass of maize cultivated on sterilized soil was 3-fold, 1.5-fold, and 1.5-fold higher for uncontaminated, moderately contaminated and highly contaminated soils respectively when compared to nonsterilized soils. Contrary to our expectation, autochthonous microflora did not improve plant growth and photosynthetic performance; in fact, they had a negative effect on those processes although they did reduce concentration of HMs in the shoots grown on contaminated soils.

Surplus phosphorus (P) above agronomic requirements can negatively affect the water status of connected surface and subsurface water bodies. The in situ stabilization of soil P through soil amendment has been recognized as an efficient way to reduce this environmental pressure. However, the mechanism of how P is stabilized during this process and how plant available P is affected are unknown. This can be achieved by sequential chemical extraction and synchrotron-based X-ray absorption near-edge structure (XANES) spectroscopy investigations. Therefore, in the present study, P-enriched calcareous and red soils were amended with alum, dolomite, and a 1:1 mixture of alum and dolomite (MAD) at a 20 g/kg soil rate, and soil properties and P fractions were measured after a 45-day period. Results showed that alum amendment significantly decreased CaCl₂-P and Olsen-P contents in calcareous and red soils when compared with dolomite. However, dolomite incorporation maintained relatively high P availability and even increased CaCl₂-P and Olsen-P contents by 1.32% and 40.5% in red soil, respectively, compared to control. Amendment with MAD was not as effectively as the alum in P stabilization. Sequential inorganic P extraction indicated that alum dominantly contributed labile P transformed to Al-P in both soils. P K-edge XANES spectroscopy measurements further explained that alum adsorbed phosphate in calcareous soil and precipitated phosphate as AlPO₄ in red soil. Results of P fractionation and Mehlich-3-extracted Ca showed that dolomite mainly adsorbed loosely bound P in calcareous soil and red soil. However, dolomite incorporation in red soil led to Al-P and Fe-P release. The P sorption isotherms showed that dolomite and alum increased soil P sorption maxima and decreased the degree of P saturation (DPS) in both soils, while dolomite declined the Langmuir bonding energy in red soil. Differences in P stabilization by alum and dolomite addition across soil types were closely related to their characteristics, and soil properties changed, especially soil pH.