The present study investigated the effect of copper on photosynthesis, antioxidant potential, and anatomical response of aquatic fern, Salvinia cucullata, with a view to ascertain its phytoremediation potential. Plants were exposed in hydroponics for 21 days to different Cu concentrations (10, 15, 20, and 30 mg/L). Significant declines in chlorophyll, carotenoids, and soluble proteins, as a function of Cu proportion were observed. Lipid peroxidation was also evident, which implied reactive oxygen species (ROS) generation. However, both root and leaf tissues responded remarkably to the ROS produced, by inducing superoxide dismutase (1.6–6.5 times), catalase (1.5–5.4 times), guaicol peroxidase (1.5–7.2 times), and ascorbyl peroxidase (1.3–4.7 times) over the control. The plant showed best phytoremedial activity within Cu range of 10–15 mg/L, with maximum accumulation of 2956 ± 82.6 μg/g dw., at 15 mg Cu/L and showed efficient root to shoot translocation (translocation factor, TF > 1) at this range, which is the stipulated minimum requirement to be a hyperaccumulator. The capacity of metal extraction from environment to leaf (extraction coefficient, EC) was also high (EC = 73–197). However, at higher doses (20–30 mg/L), the plant resorted to an exclusion strategy, whereby, more metal accumulation was observed in root than in leaf. The plant conferred suitable remediation attributes by showing minimal root and leaf anatomical damages along with high Ca peaks in both the tissues, and rapid leaf stomatal closure, all of which probably helped in the Cu induced stress mitigation. Due to its widespread availability, fast growth, ability to grow in myriads of polluted environment, and having hardy physiology, this plant can be suggested for use as a suitable Cu phytoremediator.

Magnetic cerium-doped mesoporous titanium dioxide was synthesized by combining sol–gel method and calcination using tetrabutanate and ammonium cerium nitrate as precursors and Pluronic P123 as a template coating on iron oxide covered with carbon in ethanol. The magnetic Ce-doped catalyst showed only anatase structure with a slight increase in lattice parameters compared to the undoped catalyst. The Ce LIII-edge X-ray absorption near-edge spectroscopy (XANES) spectra showed Ce³⁺, and the cerium substitution doping into titanium dioxide was proposed. Degradation of S-metolachlor in aqueous magnetic photocatalyst suspension followed (pseudo) first-order kinetics in the presence of 0.5 g L⁻¹ of γ-Fe₂O₃@[email protected] mol% Ce-mTiO₂ with a half-life of 55.18 ± 1.63 min. Fifteen degradation products were identified, and their transformation routes of the photocatalytic degradation were then proposed. Complementary toxicity assessment of the treated S-metolachlor solution was undertaken with Environment Canada’s algal microplate assay measuring growth inhibition (72-h IC₅₀) in the freshwater chlorophyte Pseudokirchneriella subcapitata. This test method revealed a significant decrease in toxicity (1.7-fold reduction after 180 min of irradiation treatment), thereby confirming that the by-products formed following photocatalysis would be less harmful from an environmental point of view. Photocatalytic degradation of S-metolachlor thus appears to hold promise as a cost-effective treatment technology to diminish the presence of this herbicide in aquatic systems.

In this work, the main objectives were to assess the mutagenic and genotoxic effects of fine particulate matter collected in an industrial influenced site in comparison with a non-industrial influenced one (rural site) and to relate the particulate matter (PM) composition to the observed genotoxic effects. At the industrial influenced site, higher concentrations of phosphates, trace metals, and polycyclic aromatic hydrocarbons (PAHs) in particles could be related to the contributions of quarries, fertilizer producer, cement plants, and tires burning. Gasoline and diesel combustion contributions were evidenced in particles collected at both sites. Particles collected under industrial influence showed a higher mutagenic potential on three tested strains of Salmonella typhimurium (TA98, YG1041, and TA102), and especially on the YG1041, compared to particles from the rural site. Furthermore, only particles collected in the vicinity of the industrial site showed a tendency to activate the SOS responses in Escherichia coli PQ37, which is indicative of DNA damage as a result of exposure of the bacteria cells to the action of mutagenic samples. The mutagenicity and genotoxicity of the industrial PM₂.₅–₀.₃ particulates may be attributed to its composition especially in organic compounds. This study showed that proximity of industries can affect local PM composition as well as PM genotoxic and mutagenic potential.

Nitrite is present as a noxious contaminant in drinking water and causes oxidative damage in various tissues of humans and animals. It is a well-known methemoglobin-forming agent that has been shown to damage blood cells. The protective effect of taurine, a semi-essential sulfur-containing amino acid, was studied on sodium nitrite (NaNO₂)-induced oxidative damage in human erythrocytes. Erythrocytes were incubated with NaNO₂, in the presence and absence of taurine, and changes in oxidative stress parameters determined. Pretreatment with taurine significantly ameliorated NaNO₂-induced oxidative damage to lipids, proteins, and plasma membrane. It also reduced the NaNO₂-induced increase in methemoglobin levels and ROS production. Taurine improved the antioxidant capacity of cells, restored the alterations in the activities of various metabolic enzymes, and prevented morphological changes in erythrocytes. Thus, taurine can be potentially used as a protective agent against the damaging effects of nitrite.

Fe(II)-mediated autotrophic denitrification with four different microbial cultures under different pH and EDTA/Fe(II) conditions was investigated in batch bioassays. Initially, the highest nitrate removal (72%) was achieved with an activated sludge inoculum. The use of pure cultures of Pseudogulbenkiania strain 2002 and Thiobacillus denitrificans resulted in a 55 and 52% nitrate removal, respectively. No denitrification was observed for a mixed culture dominated by Thiobacillus thioparus and T. denitrificans. A longer enrichment on Fe(II) and the supplementation of thiosulfate as additional electron donor were needed to stimulate the denitrifying activity of the Thiobacillus-mixed culture. A second subculture on Fe(II) as sole electron donor resulted in higher denitrification efficiencies for all microbial cultures. In particular, nitrate removal reached up to 84% with a specific nitrate removal rate of 1.160 mM·(g VSS·day)⁻¹ in the bioassays seeded with the Thiobacillus-mixed culture. All cultures were favored by decreasing the EDTA/Fe(II) molar ratio from 2.0 to 0.5. The most significant denitrification enhancement was observed for the Pseudogulbenkiania species, indicating a lower tolerance to EDTA. The two pure cultures effectively maintained denitrification at pH 7.0 and were more sensitive to a pH decrease. Conversely, the optimal pH was 6.0 for the Thiobacillus-mixed and activated sludge cultures.

In this study, the photocatalytic removal of an emerging contaminant, diclofenac (DCF) sodium, was performed using the nitrogen-doped WO₃/TiO₂-coupled oxide catalyst (WO₃/TiO₂-N). The catalyst synthesis was accomplished by a sol–gel method using tetrabutyl orthotitanate (C₁₆H₃₆O₄Ti), ammonium p-tungstate [(NH₄)₁₀H₂W₁₂O₄₂·4H₂O] and ammonium nitrate (NH₄NO₃) as the nitrogen source. For comparison, TiO₂ and WO₃/TiO₂ were also prepared under similar conditions. Analysis by X-ray diffraction (XRD), N₂ adsorption–desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV–Vis spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS) were conducted to characterize the synthesized materials. The photocatalytic efficiency of the semiconductors was determined in a batch reactor irradiated with simulated solar light. Residual and mineralized DCF were quantified by high-performance liquid chromatography, total organic carbon analysis and ion exchange chromatography. The results indicated that the tungsten atoms were dispersed on the surface of TiO₂ as WO₃. The partial substitution of oxygen by nitrogen atoms into the lattice of TiO₂ was an important factor to improve the photocatalytic efficiency of WO₃/TiO₂. Therefore, the best photocatalytic activity was obtained with the WO₃/TiO₂-N₀.₁₈ catalyst, reaching 100% DCF transformation at 250 kJ m⁻² and complete mineralization at 400 kJ m⁻² of solar-accumulated energy.

The accumulation, distribution, and speciation of contaminants, such as arsenic, in rice can be affected by soil microorganisms such as arbuscular mycorrhizal fungi (AMF). As a potential measure to control contaminant acquisition in rice, the status and performance of AMF in the field need to be investigated. Root samples of rice plants were collected in seven different cities in Guangdong, Jiangxi, Hubei, and Jiangsu Provinces in China in order to investigate the colonization rate of AMF. The total DNA of the roots was extracted, followed by PCR and sequencing, and further confirmed the existence of AMF. The highest colonization rates (19.5 ± 7.2%) were observed in samples from Huizhou City, Guangdong Province. Sequences of ribosomal DNA derived from Pingtan (PT) and Shuikou (SK) in Huizhou shared a similarity of 73 and 86% to Glomus cf. clarum Att894-7 (FM865542) and “uncultured fungus” (EF434122.1), respectively. The moisture tolerance of the AMF from different sources was tested by subjecting to different levels of water content in the soil. Only AMF from PT, SK, and LJ colonized rice under a condition of 100% of the soil water holding capacity (WHC), but not those isolated from upland plants. The AM colonization rate could be governed by the lighting conditions and temperature. AMF isolated in paddy fields has been shown to have more tolerance to moisture than other upland species. Radial oxygen loss (species and stress dependent) could be an essential factor influencing the colonization rate and requires more investigation.

Microbial fuel cells (MFCs) can use nitrate as a cathodic electron acceptor for electrochemical denitrification, yet there is little knowledge about how to apply them into current wastewater treatment process to achieve efficient nitrogen removal. In this study, two dual-chamber MFCs were integrated with an aerobic membrane bioreactor to construct a novel membrane bioelectrochemical reactor (MBER) for simultaneous nitrification and denitrification under specific aeration. The effects of chemical oxygen demand (COD) loading rate, COD/N ratio, hydraulic retention time (HRT), and external resistance on the system performance were investigated. High effluent quality was obtained in the MBER in terms of COD and ammonium. During the operation, denitrification simultaneously occurred with nitrification at the bio-cathode of the MBER, achieving a maximal nitrogen removal efficiency of 84.3 %. A maximum power density of 1.8 W/m³ and a current density of 8.5 A/m³ were achieved with a coulombic efficiency of 12.1 %. Furthermore, compared to the control system, the MBER exhibited lower membrane fouling tendency due to mixed liquor volatile suspended solids (MLVSSs) and extracellular polymeric substance (EPS) reductions, EPSp/EPSc ratio decrease, and particle size increase of the sludge. These results suggest that the MBER holds potential for efficient nitrogen removal, electricity production, and membrane fouling mitigation.

This review summarizes the environmental occurrence of new brominated flame retardants (NBFRs) and organophosphate compounds (OPs) in the environment of developing countries since 2000. The ban on the production and use of commercial formulations of polybrominated diphenyl ethers (PBDEs) have paved the way for the high use of NBFRs and OPs in consumer products to fulfill the fire safety regulations. Recent studies have shown that the ever increasing production volumes and extensive use of these chemicals as additive FRs and plasticizers have resulted into their ubiquitous occurrence in all environmental compartments. Although presumed to be safe for use and the environment, recent studies on their occurrence and persistence in the environment have raised questions. Due to the lack of awareness, research interest, and availability of technical facilities, limited scientific data is available on the occurrence of these chemicals in developing countries. In this study, we collected reported data and provide an overview of environmental occurrence of NBFRs and OPs in abiotic and biotic matrices of different developing countries. Finally, research gaps were identified with recommendations for future research work and would be useful towards the environmental management of these toxic chemicals.