The pollution of wastewater with antibiotics and antibiotics resistance genes has attracted public concerns about ecosystem and global health. Swine wastewater can contain high concentrations of antibiotics, especially sulfonamides, even after full-scale wastewater treatment. In this study, mesocosm-scale vertical flow constructed wetlands (VF-CWs) were applied to abate nutrients and antibiotics in swine wastewater containing sulfonamides. VF-CWs performed well in the removal of both nutrients and antibiotics. Sulfonamides did not influence total organic carbon (TOC) and total phosphorus (TP) removal, and even slightly enhanced NH₄⁺–N removal. High removal efficiencies (26.42–84.05%) were achieved for sulfadiazine (SDZ), sulfamethoxazole (SMX) and sulfamethazine (SMZ). Together with lab-scale sorption and biodegradation experiments, microbial degradation was found to be the most important removal mechanism for sulfonamides in VF-CWs. Sulfonamides addition increased bacterial alpha-diversity and changed microbial community structure. Moreover, antibiotics promoted antibiotic-resistant or -degrading bacteria. Bacillus, Geobacter and other seven genera were correlated with sulfonamides reduction under either aerobic or anaerobic condition. In summary, VF-CW is a suitable alternative for swine wastewater treatment, and biodegradation plays the key role in sulfonamides abatement.Main findings of the work.This was the first work to combine bacterial community analysis with microcosm experiments to uncover the major removal mechanism of sulfonamides in constructed wetlands.

Based on the goal of green and effective removal of chromium (Cr(VI)) pollution in water and the idea of treating waste with waste, rice straw (RS) was firstly and successfully used in enhancing the photoreduction of highly toxic Cr(VI) to less toxic Cr(III) by oxalic acid (Ox). Batch experiments (the effect of Ox concentration, initial Cr(VI) concentration, RS dosage and coexisting ions) in Ox + RS + UV photoreduction system were designed to investigate the reaction process. Through studying the effect of initial pH in the solution, the change of pH during the photoreduction process and the free radical scavenging test, the Cr(VI) photoreduction mechanism in Ox + RS + UV system was revealed. The role of RS in Ox + RS + UV system was also deduced by the analysis of FT-IR, XRD, Mott-Schottky and the verification test of the role of –OH and SiO₂ on RS. The results showed that RS could significantly synergize Ox to reduce Cr(VI) under UV, 1 mM Cr(VI) in aqueous solution was completely removed in 60 min by Ox + RS + UV system. The Cr(VI) photoreduction mechanism in Ox + RS + UV system consisted of multiple parts: the chemical reduction by Ox(few part), the photoreduction by Ox(some part), and the synergistic photoreduction by RS with Ox(large part). The synergism of RS in Ox + RS + UV system was mainly attributed to its components of SiO₂ and –OH of cellulose.

In this paper, the acute toxicity of monobutyl phthalate (MBP), the main hydrolysis product of dibutyl phthalate, on adult zebrafish liver antioxidant system was studied. Compared the toxicity effect of MBP and DBP by histopathology and apoptosis experiments, we speculated that the toxic effects of DBP on animals may be caused by its metabolite MBP. The results indicated that the antioxidant Nrf2-Keap1 pathway was insufficient to resist MBP-induced hepatotoxicity and led to an imbalance of membrane ion homeostasis and liver damage. Decreased cell viability, significant tissue lesions and early hepatocyte apoptosis were observed in the zebrafish liver in MBP exposure at high concentration (10 mg/L). The activities of antioxidant enzymes and ATPases in zebrafish liver were inhibited with increased malondialdehyde (MDA) content and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities. Integrated biomarker response (IBR) calculation results indicated that MBP mainly inhibited catalase (CAT) activity. Simultaneously, the expression of antioxidant-related genes (SOD, CAT, GPx, Nrf2, HO-1) was down-regulated, while apoptosis-related genes (p53, bax, cas3) were significantly up-regulated.

Bisphenol A (BPA) and bisphenol F (BPF) are widely distributed in the environment and daily consumptions, leading to exposure toward human and environmental animals. The potential risk of bisphenol analogs on pigment and skin health is not well documented. In this study, we found that 0.05 mg/L BPF (tolerated daily intake (TDI) value of BPA) affected the particle size and color density of zebrafish melanin. While BPA caused less depigmentation effect toward zebrafish with effective concentration of 5.0 mg/L. The downregulation of melanin synthases induced by BPF is associated with the reduction in melanin. Molecular dynamics indicated that both BPF and BPA could act as ligands of zebrafish and human Tyr family proteins; however, these compounds have completely different energetics and spatial steric effects, potentially explaining their varying depigmentation effects. Additionally, an in vitro assay using A375 melanoma cells demonstrated that the inhibitory effect of BPF on human melanin production was primarily attributed to Tyr inhibition. These findings provide an important basis for understanding the molecular mechanisms of BPF and BPA in melanin inhibition, and the results reflect the skin pigmentation interference risk of these compounds, which are ubiquitous in everyday personal products.

Halogenated polycyclic aromatic hydrocarbon (HPAH) concentrations in tissues from three tuna species Thunnus albacares (yellowfin tuna), Katsuwonus pelamis (skipjack tuna), and Auxis thazard (frigate tuna) were determined by high-resolution gas chromatography Orbitrap mass spectrometry. The tuna samples were collected from the Indian Ocean. The instrument conditions gave high mass accuracy at 0.9 m/z isolation width of the mass filter and a mass error of <±1.0 ppm for many HPAHs. A total of 29 of the 30 targets chlorinated PAHs (ClPAHs) and 20 of the 21 targets brominated PAHs (BrPAHs) were detected in the tuna muscle samples. The mean total ClPAH, BrPAH and PAH concentrations for tuna were 127.2, 156.6 and 682.8 ng/g lipid weight, respectively. The mean total ClPAH and BrPAH concentrations (ng/g lipid weight) in the tuna were considerably lower than that of PAH concentrations. The mean total ClPAH, BrPAH and PAH concentrations in T. albacares respectively were 185.8, 249.2 and 784.1 ng/g lipid weight, irrespective of the body sizes. The mean total ClPAH, BrPAH and PAH concentrations in K. pelamis respectively were 45.1, 24.8 and 555.6 ng/g lipid weight. The mean total ClPAH, BrPAH and PAH concentrations in A. thazard respectively were 34.09, 4.73 and 433.24 ng/g lipid weight. The total ClPAH concentrations and body weights significantly positively correlated for T. albacares. The mean total ClPAH concentration in white muscles was significantly higher (p < 0.05) for large than for small T. albacares. This suggests ClPAHs could bioaccumulate in T. albacares, possibly because they are poorly metabolized. The chlorinated phenanthrene and pyrene concentrations indicated tuna accumulate these compounds increasingly effectively as the tuna grow. This was the first time large numbers of HPAHs were found in biological samples. HPAHs may adversely affect the health of humans consuming tuna.

The increased occurrence of Mercury (Hg II) contaminant has caused environmental and health concerns worldwide. Removal of Hg(II) from water is of significant interest, in particular if these can be coupled in a manner of detection. Here, a novel activated carbon (AC) adsorbent and a fast detection device to form a closed-cycle strategy was developed. The synthesis of conjugates of streptavidin-biotinylated DNA probes modified gold nanoparticle was used with lateral flow biosensors for Hg(II) detection. A quantification was completed via a self-developed smartphone app and its limit of detection was 2.53 nM. Moreover, AC was activated with a new activating agent of diammonium hydrogen phosphate. The adsorbent was characterized and determined to have an amorphous microporous structure with a high surface area (1076.5 m² g⁻¹) and demonstrated excellent removal efficiency (99.99%) and adsorption capacity (∼100 mg g⁻¹) for Hg(II). The kinetics of the pseudo-second-order model and the mechanisms of electrostatic adsorption, ion exchange, and complex reactions are provided. The proposed closed-cycle strategy can be useful for early, fast, and mobile detection of Hg (II) pollution, followed by its effective removal during water treatment.

Anthropogenic pollution of the Arctic atmosphere is of great interest due to the vulnerability of the Arctic ecosystems, as well as the processes of global transport and accumulation of atmospheric aerosols at high latitudes under conditions of cold climate. The present work throws light upon chemical composition of Arctic snow as a natural deposition matrix for atmospheric semi-volatile pollutants taken from the northernmost Arctic archipelago - Franz Josef Land, which is least affected by local sources of pollution and being a unique unstudied environmental object. The used methodology involved the liquid-liquid extraction of snow samples with dichloromethane and combination of targeted and non-targeted analyses of semi-volatile organic compounds with comprehensive two-dimensional gas chromatography – high-resolution mass spectrometry. While almost none of the known priority pollutants (except three dialkylphthalates) were identified in the studied samples, non-targeted screening revealed a specific class of biomass burning biomarkers – fatty amides with oleamide being the major component among them. Some peculiar organic pollutants (N,N-dimethylcyclohexylamine and N,N-dimethylbenzylamine) were identified in few samples.First results on the semi volatile pollutants in Franz Joseph Land snow were obtained using the most reliable GC × GC-HRMS non-target analysis.

In shallow eutrophic lakes, metal remobilization is closely related to the resuspension and eutrophication. An improved understanding of metal dynamics by biogeochemical processes is essential for effective management strategies. We measured concentrations of nine metals (Cr, Cu, Zn, Ni, Pb, Fe, Al, Mg, and Mn) in water and sediments during seven periods from 2014 to 2018 in northern Lake Taihu, to investigate the metal pollution status, spatial distributions, mineral constituents, and their interactions with P. Moreover, an automatic weather station and online multi-sensor systems were used to measure meteorological and physicochemical parameters. Combining these measurements, we analyzed the controlling factors of metal dynamics. Shallow and eutrophic northern Lake Taihu presents more serious metal pollution in sediments than the average of lakes in Jiangsu Province. We found chronic and acute toxicity levels of dissolved Pb and Zn (respectively), compared with US-EPA “National Recommended Water Quality Criteria”. Suspended particles and sediment have been polluted in different degrees from uncontaminated to extremely contaminated according to German pollution grade by LAWA (Bund/Länder-Arbeitsgemeinschaft Wasser). Polluted particles might pose a risk due to high resuspension rate and intense algal activity in shallow eutrophic lakes. Suspended particles have similar mineral constituents to sediments and increased with increasing wind velocity. Al, Fe, Mg, and Mn in the sediment were rarely affected by anthropogenic pollution according to the geoaccumulation index. Among them, Mn dynamics is very likely associated with algae. Micronutrient uptake by algal will affect the migration of metals and intensifies their remobilization. Intensive pollution of most particulate metals were in the industrialized and down-wind area, where algae form mats and decompose. Moreover, algal decomposition induced low-oxygen might stimulate the release of metals from sediment. Improving the eutrophication status, dredging sediment, and salvaging cyanobacteria biomass are possible ways to remove or reduce metal contaminations.

The radial translocation of cadmium (Cd) from the root to the shoot is one of the major processes affecting Cd accumulation in rice (Oryza sativa L.) grains, but few studies have focused on Cd apoplastic transport in rice. The aim of this study was to determine how apoplastic barriers affect Cd translocation via the apoplastic pathway, Cd accumulation levels in upper parts (shoot and grains) of rice cultivars, and the possible mechanism involved. Hydroponic and soil pot trials were conducted to study the development and chemical constituents of apoplastic barriers and their permeability to bypass flow, and to determine Cd localization in the roots of rice cultivars with different Cd-accumulating characteristics. The Cd accumulation in upper parts was positively correlated with bypass flow in the root and the apparent Cd concentration in the xylem, indicating that the apoplastic pathway may play an important role in Cd root-shoot translocation in rice. Apoplastic barriers were deposited closer to the root tip and were thicker in low Cd-accumulating cultivars than in high Cd-accumulating cultivars. The amounts and rates of increase in lignin and suberin were significantly higher in ZD14 (a low Cd-accumulating cultivar) than in FYXZ (a high Cd-accumulating cultivar) under Cd stress, indicating that stronger barriers were induced by Cd in ZD14. The stronger and earlier formation of barriers in the low Cd-accumulating cultivar decreased bypass flow more efficiently, so that more Cd was retained in the root during apoplastic translocation. This was confirmed by localization analyses of Cd in root transverse sections. These results suggest that apoplastic barriers reduce Cd root-to-shoot translocation via the apoplastic pathway, leading to lower Cd accumulation in the upper parts of rice plants. Bypass flow may have the potential to be used as a rapid screening indicator for low Cd-accumulating rice cultivars.

The strict Clean Air Action Plan has been in place by central and local government in China since 2013 to alleviate haze pollution. In response to implementation of the Plan, daytime PM₂.₅ (particulate matter with aerodynamic diameter less than 2.5 μm) showed significant downward trends from 2015 to 2019, with the largest reduction during spring and winter in the North China Plain. Unlike PM₂.₅, O₃ (ozone) showed a general increasing trend, reaching 29.7 μg m⁻³ on summer afternoons. Increased O₃ and reduced PM₂.₅ simultaneously occurred in more than half of Chinese cities, increasing to approximately three-fourths in summer. Declining trends in both PM₂.₅ and O₃ occurred in only a few cities, varying from 19.1% of cities in summer to 33.7% in fall. Meteorological variables helped to decrease PM₂.₅ and O₃ in some cities and increase PM₂.₅ and O₃ in others, which is closely related to terrain. High wind speed and 24 h changing pressure favored PM₂.₅ dispersion and dilution, especially in winter in southern China. However, O₃ was mainly affected by 24 h maximum temperature over most cities. Soil temperature was found to be a key factor modulating air pollution. Its impact on PM₂.₅ concentrations depended largely on soil depth and seasons; spring and fall soil temperature at 80 cm below the surface had largely negative impacts. Compared with PM₂.₅, O₃ was more significantly affected by soil temperature, with the largest impact at 20 cm below the surface and with less seasonal variation.