Polyacrylonitrile polymer (PAN), a common representative textile material and a microplastic, has significant influence on phytoplankton algae, especially with co-exposure with other pollutants, e.g. Cu²⁺. In the present study, we carried out experiments to reveal the population size variation trends of Chlorella pyrenoidosa over time (during a whole growth cycle of 6 days) under PAN and/or Cu²⁺. The levels of pigments (chlorophyll a, b, total chlorophyll and carotenoids), chlorophyll a fluorescence parameters, and other physiological and biochemical indices, containing total protein measurements of H₂O₂, catalase (CAT), and malondialdehyde (MDA) under different treatment groups were measured to explain the physio-ecological mechanism of the effect of PAN and/or Cu²⁺ on the growth of C. pyrenoidosa. The results showed that PAN, Cu²⁺ and the combination of PAN and Cu²⁺ inhibited the growth of C. pyrenoidosa. Chlorophyll a and b decreased significantly with increasing levels of pollutants (PAN and/or Cu²⁺); however, the carotenoid levels increased with increasing levels of pollutants (PAN and/or Cu²⁺) for the first three cultivation days. The oxygen-evolving complexes (OECs) of C. pyrenoidosa had been damaged under Cu²⁺ pollution. The results also showed that CAT activity, MDA content and H₂O₂ activity of C. pyrenoidosa increased with increasing levels of pollutants (PAN and/or Cu²⁺); however, total protein content decreased with increasing levels of pollutants (PAN and/or Cu²⁺) at the first cultivation day. These results indicate that pollutants (PAN and/or Cu²⁺) are harmful to the growth of the C. pyrenoidosa population and negatively affect the levels and function of the pigments in C. pyrenoidosa by decreasing chlorophyll a and b levels, increasing carotenoid levels, and increasing antioxidant enzyme activity.

Etoxazole is an organofluorine insecticide widely used in agriculture. Exposure to insecticides is a serious environmental problem owing to their cytotoxic effects in humans and animals. Reproductive toxicity of various organofluorine insecticides have been shown in previous studies. However, few studies have evaluated the toxicity of etoxazole in mammals. We aimed to examine the toxic effects of etoxazole in porcine trophectoderm (pTr) and uterine luminal epithelial (pLE) cells. To estimate the effects of etoxazole, we conducted assays after treatment with multiple concentration of etoxazole (0, 2, 4, 6 and 9 μM) to pTr and pLE cells for 0–72 h. Etoxazole decreased the cell proliferation, viability, and migration of pTr and pLE cells. Further, etoxazole induced apoptosis via cell cycle arrest and disruption of mitochondrial membrane potential. We also found that pro-apoptotic proteins and endoplasmic reticulum (ER) stress-response proteins were activated in response to etoxazole. Finally, we observed that etoxazole altered the PI3K/AKT and MAPK signaling pathways and the mRNA expression of genes associated with implantation. Collectively, these results suggest that etoxazole disrupts normal cellular physiology and might cause early implantation failure.

A self-assembly method was adopted to synthesize loading architecture of ZnO/g-C₃N₄ heterojunction composites by hybridization of g-C₃N₄ nanosheets and ZnO nanoparticles utilizing a refluxing method at a low temperature. More importantly, we provided a novel route to regulate the π-π restacking thickness of the g-C₃N₄ nanosheets among ZnO/g-C₃N₄ composites by the controlling the refluxing time in the ethanol solution, which can optimize the surface hybrid structure, optical response and photocatalytic activity. Among all of samples, ZnO/g-C₃N₄ composites with a refluxing 12 h showed the enhancement of photocatalytic activity. The enhanced visible light photocatalytic activity of ZCN-12 composites can be ascribed to the synergistic effects of the construction of hybrid structures, reduction of structural defects of g-C₃N₄ nanosheets and suitable π-π restacking g-C₃N₄ nanosheets loading thickness.

Occurrence, behavior, and fate of 11 OPEs in multiple environmental matrices, which include air, rainwater, dustfall, paddy soil, irrigation water, and rice plants from nine subtropical paddy fields of South China, were investigated. The total concentrations of 11 OPEs (∑₁₁OPEs) in all matrices are generally higher in the urban areas than in rural areas, and they are higher in summer than in fall. However, both urban and rural areas showed a similar composition profile of OPEs, indicating that the OPEs come from similar sources in the two areas. Except for irrigation water, significant positive correlations of ∑₁₁OPEs were observed between air and the other five matrices. The exchange and partition of OPEs among air, soil, and water demonstrate that most of OPEs were transferred from air into water and soil, and from water into soil. Thus, the air may be an important source of OPEs in the paddy fields, and the soil may act as a principal environmental reservoir of OPEs. The contribution of air-soil exchange, atmospheric deposition (rainwater plus dustfall), and irrigation water to the total input fluxes of OPEs (2100 ± 980 ng/m²/day) reached an average of 19%, 38% (37% + 1%), and 43%, respectively. The water (rainwater plus irrigation water) is the primary medium transferring the OPEs into the paddy fields and contributed to the input flux by 80%. Output flux of OPEs via mature rice plants was about 220 μg/m², 2% of which were presented in rice, and the remaining 98% may be re-released into the environment through the pathway of straw turnover or burning. Dietary exposure via rice was much higher than inhalation exposure, dust ingestion, and dermal absorption via dust. However, no data shows that all of the intakes via the four exposure pathways could cause the risks to human health at present.

After exposure of soils to anthropogenic organic chemicals non-extractable residues (NER) can be formed. The quantitative proportion of a compound which remains non-extractable is operationally defined by the extraction procedure employed and can be quantified only when using isotope labelled compounds (e.g. ¹⁴C or ¹³C). In Germany and the EU, there is no standardised procedure, how to determine NER, especially when different legal regulations apply. Consequently, the comparability of NER data is low. Hence, a major task of this study was the development of a general approach for the quantification of non-extractable residues (NER) in soils using radiotracer analysis.For that, extraction efficiencies were determined for 42 non-labelled organic chemicals spiked onto 3 soils applying a number of extraction techniques and conditions, developing an extraction procedure which provides high extraction efficiencies and a low variability for a broad spectrum of analytes.Additionally, NER generated within soil transformation studies according to OECD 307 using ¹⁴C-triclosan, ¹⁴C-fenoxycarb and ¹⁴C-acetaminophen were analysed using sequential batch extraction and pressurised liquid extraction (PLE). Depending on the extraction procedure used, the NER fraction related to ¹⁴C-triclosan in a soil varied greatly between 96% and 28%.In this study a widely universal extraction procedure was developed to improve the comparability of the NER data and limit overestimation of NER, which can be of enormous consequence for the assessment of persistence and environmental risk of organic chemicals. Furthermore, silylation, EDTA-extraction and HCl-treatment were compared regarding a further analysis of NER using radiotracer analysis.

Mercury (Hg) is a toxic and persistent pollutant and has long-term impacts on ecological systems and human health. Coal-fired power plants (CFPPs) are the main source of anthropogenic Hg emission, and the emitted atmospheric Hg is deposited to the surrounding environments which causes soil pollution. To assess the effects of atmospheric Hg from CFPPs in China on the temperate steppe, Hg contents in the topsoil and subsoil were analyzed for samples collected from 80 sites in central Inner Mongolia during 2012–2015. The average content of Hg in topsoil and subsoil were 14.9 ± 10.4 μg kg⁻¹ and 8.9 ± 5.8 μg kg⁻¹, respectively. The principal components analysis (PCA) indicated that the soil organic matter content and atmospheric deposition were the main factors determining soil Hg content in Inner Mongolia. We used the power plant impact factor (PPIF) to evaluate the impacts of the surrounding CFPPs. The PPIF results showed the most positive correlation with Hg content in topsoil at more than 400 km distances, indicating that the contribution of the long-range transport of Hg emitted from CFPPs is regional in scale. Considering the potential of Hg accumulation in soil, long-term and regional measurements of soil Hg and stricter emission-limit standards for power plants should be implemented to control soil Hg pollution in China.

Abundance, composition, and distribution of macro-litter found on the seafloor of the Strait of Sicily between 10 and 800 m depth has been studied using data collected by bottom trawl surveys MEDITS from 2015 to 2019. Three waste categories based on the items use were considered: single-use, fishing-related and generic-use. Over 600 sampling sites, just 14% of these were litter-free. The five-years average density of seafloor litter was 79.6 items/km² and ranged between 46.8 in 2019 and 118.1 items/km² in 2015. The predominant waste type was plastic (58% of all items). Regardless of material type, single-use items were a dominant (60% of items) and widespread (79% of hauls) fraction of litter with a mean density of 48.4 items/km². Fishing-related items accounted for 12% of total litter items. Percentage of dirty hauls and litter density increased with depth. Analysis of the relation density-depth indicates a progressive increase of litter density beyond depth values situated within the interval 234–477 m depending on the litter category. A significant decrease in litter density by categories was observed over the period. Patterns of spatial distribution at the higher depths (200–80 0m) resulted stable over the years. Density hotspots of fishing-related items were found where the fishing activity that uses fish aggregating devices (FADs) is practised and in the proximity of rocky banks. Single-use and generic-use objects densities were greater on the seafloor along main maritime routes than other areas. Comparisons between the percentage of hauls littered with anthropic waste from the mid-1990s against those in 2018–19 highlighted an increase of about 10.8% and 15.3% for single-use items and fishing-related items respectively, and a decrease of 18.6% for generic-use items. This study provides a snapshot of the current situation of littering in the central Mediterranean Sea and represents a solid baseline against which the effectiveness of current and future mitigation strategies of the litter impact on marine environment can be measured.

Breaking of biochar during compaction of amended soil in roadside biofilters or landfill cover can affect infiltration and pollutant removal capacity. It is unknown how the initial biochar size affects the biochar breaking, clogging potential, and contaminant removal capacity of the biochar-amended soil. We compacted a mixture of coarse sand and biochar with sizes smaller than, similar to, or larger than the sand in columns and applied stormwater contaminated with E. coli. Packing columns with biochar pre-coated with a dye and analyzing the dye concentration in the broken biochar particles eluted from the columns, we proved that biochar predominantly breaks under compaction by disintegration or splitting, not by abrasion. Increases in biochar size decrease the likelihood of biochar breaking. We attribute this result to the effective dissipation of compaction energy through a greater number of contact points between a large biochar particle and the adjacent particles. Most of the broken biochar particles are deposited in the pore spaces of the background geomedia, resulting in an exponential decrease in hydraulic conductivity of amended sand with an increase in suspended sediment loading. The clogging rate was higher in the columns with small biochar. The columns with small biochar also exhibited high E. coli removal capacity, partly because of an increase in bacterial straining at reduced pore size after compaction. These results are useful in selecting appropriate biochar size for its application in soils and roadside biofilters for stormwater treatment.

Pesticides scarcely exist as individual compounds in the water ecosystem, but rather as mixtures of multiple chemicals at relatively low concentrations. In this study, we aimed to explore the mixture toxic effects of fludioxonil (FLU) and triadimefon (TRI) on zebrafish (Danio rerio) by employing different toxicological endpoints. Results revealed that the 96-h LC₅₀ values of FLU to D. rerio at multiple developmental stages ranged from 0.055 (0.039–0.086) to 0.61 (0.33–0.83) mg L⁻¹, which were less than those of TRI ranging from 3.08 (1.84–5.96) to 9.75 (5.99–14.78) mg L⁻¹. Mixtures of FLU and TRI exerted synergistic effects on embryonic zebrafish. Activities of total superoxide dismutase (T-SOD) and catalase (CAT) were markedly altered in most of the individual and pesticide mixture treatments compared with the control. The expressions of 16 genes involved in oxidative stress, cellular apoptosis, immune system and endocrine system displayed that embryonic zebrafish were affected by the individual pesticides and their mixtures, and greater variations of four genes (ERɑ, Tnf, IL and bax) were found when exposed to pesticide mixtures compared with their individual compounds. Therefore, more studies on mixture toxicities among different pesticides should be taken as a priority when evaluating their ecological risk.

To understand the effect of reaction temperature on sulfur during hydrothermal carbonization (HTC) of sewage sludge (SS), seven group of temperature (180–300 °C) were chosen to investigate the distributions and evolution of sulfur-containing compounds in hydrochar and the liquid products. Elemental analysis, X-ray photoelectron spectroscopy (XPS), and X-Ray powder diffraction (XRD) were used to characterize the distribution of sulfur in hydrochar. The concentrations of sulfate ions and sulfide were determined in the liquid sample. The experimental results showed that as the temperature increased, the O/C ratio decreased because of the improved carbonization degree of SS. After hydrothermal carbonization, 90% of the sulfur in SS remained in hydrochar. As the temperature increased, the amount of sulfur in the liquid, mainly in the form of sulfate ions, tended to decrease. However, the experimental results for the gas phase were the opposite of the liquid phase.