Human interferences have caused groundwater contamination in alluvial aquifers which subsequently affects the health of exposed population. In the present study, 74 groundwater samples from the semi-arid region of Panipat district, falling under Yamuna sub-basin, India was evaluated to know the potential non-carcinogenic human health risk in local adult and child population. The major objective of the present study was to know the non-carcinogenic human health risk due to intake of fluoride and nitrate contaminated water, using two different approaches: deterministic and probabilistic (Monte Carlo simulation). The values of hazard quotient (HQ) determined by deterministic as well as probabilistic approach were nearly identical. The hazard index (HI) value of 40.8% samples was above the unity in case of adults while 69.7% samples indicated HI value greater than unity for children thus indicating children are more prone to non-carcinogenic health risk than the adult population. Sensitivity analysis was performed to identify the influence of the non-carcinogenic human health risk predictor variables for the prediction of risk and concentration factor (CF) was the most influential variable. Multivariate statistical techniques were employed to know the positive and negative relationship of fluoride and nitrate with other parameters. Results of principal component analysis/factor analysis (PCA/FA) indicated that the concentration of fluoride is controlled by the presence of calcium due to their negative correlation in groundwater samples. The hierarchical agglomerative cluster analysis (HCA) also supported the outcome of PCA/FA and both indicated anthropogenic sources of fluoride and nitrate in groundwater.

Dibutyl phthalate (DBP) is widely used as plasticizer and has been detected in the environment, posing a threat to animal health. However, the effects of DBP on agricultural microbiomes are not known. In this study, DBP levels in black soil were evaluated, and the impact of DBP contamination on the uptake and metabolism of sugars in microbes was assessed by glucose absorption tests, metaproteomics, metabolomics, enzyme activity assays and computational simulation analysis. The results indicated that DBP contamination accelerated glucose consumption and upregulated the expression of porins and periplasmic monosaccharide ATP-binding cassette (ABC) transporter solute-binding proteins (SBPs). DBP and its metabolic intermediates (carboxymuconate and butanol) may form a stable complex with sugar transporters and enhance the rigidity and stability of these proteins. Sugar metabolism resulting in the generation of ATP and reducing agent (NADPH), as well as the expression of some key enzymes (dehydrogenases) were also upregulated by DBP treatment. Moreover, a diverse bacterial community appears to utilize sugar, suggesting that there are widespread effects of DBP contamination on soil microbial ecosystems. The results of this study provide a theoretical basis for investigating the toxicological effects of DBP on microbes in black soil.

Microplastics (MPs) pollution in the marine environment has attracted considerable global attention. However, the colonization of microorganisms on mariculture-derived MPs and their effects on mariculture remain poorly understood. In this study, the MPs (fishing nets, foams and floats) and a natural substrate, within size ranges (1–4 mm), were then incubated for 21 days in Sungo Bay (China), and the composition and diversity of bacterial communities attached on all substrates were investigated. Results showed that bacterial communities on MPs mainly originated from their surrounding seawater and sediment, with an average contribution on total MPs adherent population of 47.91% and 37.33%, respectively. Principle coordinate analysis showed that community similarity between MPs and surrounding seawater decreased with exposure time. In addition, lower average bacterial community diversity and higher relative abundances of bacteria from the genera Vibrio, Pseudoalteromonas and Alteromonas on MPs than those in their surrounding seawater and sediments indicated that MPs might enrich potential pathogens and bacteria related with carbohydrate metabolism. They are responsible for the significant differences in KEGG Orthology pathways (infectious disease and carbohydrate metabolism) between MPs and seawater. The KO pathway (Infectious Diseases) associated with MPs was also significantly higher than those with feathers in the nearshore area. MPs might be vectors for enrichment of potentially pathogenic Vibrio, and enhance the ecological risk of MPs to mariculture industry.

This study assessed the sources, magnitudes, and chemical compositions of household air pollution (HAP) and personal exposure in traditional Tibetan households. We measured 24-h personal exposures to PM₂.₅ and kitchen area black carbon (BC) concentrations, using MicroPEMs and microAeths, respectively. Particulate polycyclic aromatic hydrocarbon (PAH) and inorganic element concentrations were quantified via post analyses of a subset of MicroPEM sample filters. Household surveys regarding participant demographics, cookstove usage, household fuel, cooking behaviors, and lifestyles were collected. The results reaffirm that burning firewood and yak dung, mainly for cooking, leads to high PM₂.₅ and BC exposures. The geometric mean concentration (95% confidence interval, CI) was 74.3 (53.6, 103) μg/m³ for PM₂.₅ and the arithmetic mean ± standard deviation (SD) concentration was 4.90 ± 5.01 μg/m³ for BC and 292 ± 364 ng/m³ for 15 identified PAHs, respectively. The arithmetic mean ± SD of mass concentrations of 24 detected elements ranged from 0.76 ± 0.91 ng/m³ (Co) to 1.31 ± 1.35 μg/m³ (Si). Our statistical analyses further illustrated that the high concentrations of PM₂.₅, BC, and most PAHs and metals, are significantly associated with nomadic village, poorer stove/chimney conditions and yak dung burning. The results from this study show that substantial HAP exposure is prevalent in Tibetan households and requires immediate actions to mitigate potential negative environmental health impacts. The observational data also revealed the possibility of other important sources (e.g. traffic and garbage burning) that have contributed to personal exposures. These findings improve our understanding of HAP exposure and potential health risks in Tibetan communities and will help inform strategies for reducing HAP in Tibetan households and beyond.

Clonal plants can share information and resources among connected ramets (asexual individuals). Such clonal integration can promote ramet growth, which may further influence soil microbial communities in the rooting zone. Crude oil contamination can negatively affect plant growth and alter soil microbial community composition. However, we still know little about how clonal integration affects soil microbial communities, especially under crude oil contamination. In a coastal wetland, ramets of the rhizomatous plant Phragmites australis in circular plots (60 cm in diameter) were subjected to 0, 5 and 10 mm depth of crude oil, and the rhizomes at the edge of the plots were either severed (preventing clonal integration) or left intact (allowing clonal integration). After three years of treatment, we analysed in each plot soil physiochemical properties and soil microbial community composition. The alpha-diversity of the soil microbial communities did not differ between intact and severed plots, but was overall lower in 10-mm than in 0-mm and 5-mm oil plots. Considering all three oil treatments together, soil microbial community dissimilarity (beta-diversity) was positively correlated with soil property distance in both severed and intact plots. Considering the three oil treatments separately, this pattern was also observed in 10-mm oil plots, but not in 0-mm or 5-mm oil plots. The soil microbial community composition was more sensitive to the oil addition than to the clonal integration. Moreover, the relative abundance of the nitrogen-cycling bacterial taxa was lower in intact than in severed plots, and that of the oil-degrading bacterial taxa increased with increasing oil-addition levels. Our results indicate that clonal integration and oil contamination can influence soil microbial communities independently through changing the relative abundance of the component bacteria taxa, which has important implications for ecosystem functions of the soil food web mediated by clonal plants.

In this study, the light absorption properties of fine organic aerosols from the burning emissions of four biomass materials were examined using UV-spectrophotometry and Aethalometer-measurements, respectively. For wood chips and palm trees, the burning experiments were carried out with different combustion temperatures (200, 250, and 300 οC) in an adjustable, electrically heated combustor. The light absorptions of water and methanol extracts of aerosols, and smoke particles showed strong spectral dependence on the burning emissions of all biomass materials. However, the burning aerosols of wood chips showed stronger absorption than those of the other biomass burning (BB) emissions. For the burning aerosols of wood chips and palm trees, organic carbon/elemental carbon (OC/EC) decreased as the combustion temperature increased from 200 to 300 °C. Absorption Ångström exponent (AAE) values tended to decrease when combustion temperature increased for smoke aerosols and methanol extracts in smoke samples. The mass absorption efficiency at 365 nm (MAE₃₆₅, m² g⁻¹∙C⁻¹) of water- and methanol-extractable OC fractions was highest in wood chip burning smoke samples. MAE₃₆₅ values of methanol extracts for rice straw, pine needles, wood chips, and palm trees burning emission samples were 1.35, 0.92, 2.36–3.37, and 0.86–1.42, respectively. For wood chip and palm tree burning emissions, AAE₃₂₀–₄₃₀ₙₘ values of methanol extracts were strongly correlated with OC/EC (i.e., combustion temperature) with slopes of 0.11 (p < 0.001) and 0.02 (p < 0.001), and R² values of 0.87 and 0.74, respectively. Moreover, a linear regression between MAE₃₆₅ of methanol extractable OC and OC/EC showed slopes of −0.05 (p < 0.001) and −0.004 (p < 0.001) and R² of 0.72 and 0.74, respectively. The results of this study clearly demonstrate that burning condition and biomass type influence the light absorption properties of organic aerosols from BB emissions.

Triphenyl phosphate (TPHP) is an organophosphate ester (OPE) used as a flame retardant (FR) and plasticizer. TPHP has previously been shown to disrupt behaviour in fish and mammals, but to our knowledge, this is the first study on the behavioural effects of TPHP in birds. Early life stage Japanese quail (Coturnix japonica) were exposed to nominal doses of 0 ng/g (vehicle-control), 5 ng/g (low dose), 50 ng/g (mid dose), and 100 ng/g (high dose) TPHP, both as embryos (via air cell injection prior to incubation) and as chicks (via daily gavage until 5 days post-hatch). The low dose reflects TPHP levels recorded in wild avian eggs, but actual environmental exposure levels may be higher given that TPHP is known to be rapidly metabolized in birds. We previously reported that the chicks exposed to TPHP in this study experienced reduced growth and resting metabolic rate, and sex-specific changes in thyroid function. The current study focuses on behavioural endpoints. We found that high-TPHP chicks exhibited less neophobia than vehicle-controls, and low-TPHP chicks exhibited more aggression towards conspecifics. No differences were observed in the responses of Japanese quail chicks to activity or tonic immobility (fear response) tests. These data add weight of evidence to previous findings suggesting that TPHP, among other OPEs, can disrupt ecologically-relevant behaviours in exposed vertebrates.

Nanoplastics are inevitably released into aquatic environments due to their extensive use and the continuous fragmentation of plastics. Therefore, it is imperative to understand the aggregation behaviours that determine the transport and fate of nanoplastics in aquatic environments. In this study, the effects of various metal cations, pH, aging and extracellular polymeric substances (EPS) on the aggregation of polystyrene nanoplastics (nano-PS) in aqueous solutions were systematically evaluated based on aggregation kinetics experiments and Derjaguin–Landau–Verwey–Overbeek (DLVO) theoretical calculation. The concentration, valence and hydration ability of metal cations jointly affected the aggregation of nano-PS. The critical coagulation concentration (CCC) of nano-PS was significantly higher than the ionic strengths in aquatic environments, indicating that the aggregation rate of nano-PS is relatively low in aquatic environments. The results of the aggregation kinetics experiments were consistent with DLVO theory, which showed that the energy barrier of nano-PS was dependent on electrostatic repulsion forces and van der Waals forces, and increased with pH. Nano-PS was artificially aged by UV-H₂O₂, which reduced the hydrophobic nature of the particle surfaces, consequently enhancing the stability of the nanoplastics. EPS (excreted from Chlorella pyrenoidosa) decreased the aggregation rates of nano-PS due to steric effects, which was confirmed by the extend DLVO model. Our results highlight the high stability of nano-PS in aquatic environments, which could help facilitate the evaluation of their environmental impact.

Photocatalysis is a promising method to eliminate hexavalent uranium (U(Ⅵ)) and recycle it from wastewater. However, most of researched photocatalysts are metal-contained, inactive in visible light, and inconvenient to recycle, which unfortunately impedes the further utilization of photocatalytic technology in U(Ⅵ) pollution treatment. Herein, g-C₃N₄ isotype heterojunction with interpenetrated tri-s-triazine structure (ipCN) was prepared by inserting urea into the interlayer of tri-s-triazine planes of thiourea-derived g-C₃N₄ and in-site thermal treating. The synthesized nanocomposites were used to convert soluble U(Ⅵ) ions into U(Ⅳ) sediment under visible light. Experimental and characterization results reveal that ipCN possess larger BET surface area, more negative-charged surface, higher U(Ⅵ) adsorption capability, and more efficient mass diffusion and charges transfer properties. With these excellent characteristics, nearly 98% U(Ⅵ) could be removed within 20 min over ipCN₅:₁ and 92% photoreduction efficiency could also be kept after 7 cycle uses, which were equal to or even superior than most reported metal-based photocatalysts. It is also proven that the configuration of U(Ⅵ) and photogenerated ·O₂⁻ play a significant role in the photocatalytic U(Ⅵ) reduction process, with (UO₂)ₓ(OH)y²ˣ⁻ʸ are more prone to be adsorbed and the photoinduced process of ·O₂⁻ will steal electrons from photocatalysts. Furthermore, with the self-generated ·O₂⁻ and H₂O₂, a green and facile regeneration process of photocatalysts was proposed This work provides a promising scheme to extract U(Ⅵ) from the perspectives of photocatalysts exploitation, photocatalytic reduction, and photocatalysts regeneration, which is meaningful for the sustainable U(Ⅵ) resource recovery and U(Ⅵ) pollution purification.