The marine environment of coastal Shandong Peninsula has been significantly influenced by anthropogenic activities due to the rapid industrialization and economic development in the past decades. However, the sedimentary records of PTEs in the North Yellow Sea have rarely been reported. In this study, a 209-cm-long sediment core was collected off the northern coast of Shandong Peninsula, analyzed for grain size and elemental compositions, and assessed using EF, Igₑₒ and several numerical Sediment Quality Guidelines (SQGs). The EF and Igₑₒ results suggested that sediment profile could be slightly to moderately polluted with As and Sb, while ecological risk assessment using SQGs showed that As, Cr, Sb and Ni in the sediment profile may have a moderate incidence of toxicity. Our results highlighted the nonnegligible ecological risk of Sb in sediments of North Yellow Sea, and great importance should be attached to the fact that many PTEs may also pose a potential ecological risk to the aquatic organisms, even though their concentrations meet the standards of the Marine Sediments Quality (MSQ). Moreover, the reconstructed PTEs record showed a dramatic increase over the past 250 years, which could be related to the intense anthropogenic activities since the Industrial Revolution. The multivariate statistical analysis results indicated that Co, Cr, Cu, Pb, Ni and Zn may be mainly related to the natural origin, while As and Sb could be influenced by both natural weathering sources and anthropogenic activities. This study provides more insights into the historical record of PTEs in the North Yellow Sea, and lays foundation for future comparison of PTEs sedimentary records.

To date, knowledge of internal human exposure to BPA and its analogues (particularly bisphenol S and bisphenol F, etc.) remains limited. In the present study, a method involving dispersive solid-phase extraction and LC/MS was proposed to investigate the contamination levels of 28 precursor bisphenols and 9 major metabolites in serum. The critical variables of preparation method were screened out by Plackett-Burman design and further optimized by central composite design. Left in optimal conditions, a total of 286 samples consisting of 153 males and 133 females were analyzed. The results showed that BPA dominated over all the cases with the highest positive rate (82.2% of all the surveyed people), and totally four metabolites (BPA β-D-glucuronide, BPA monosulfate, BPA bis-(β-D-glucuronide) and BPS monosulfate) were detectable. The occurrence of BPA bis-(β-D-glucuronide) in serum is reported for the first time and its higher positive rate and contamination concentrations suggested that it may be a more important metabolite of BPA than others. Negligible potential risk of health effects to blood donors was observed, since the estimated exposure levels (mean 32.1 ng/kg bw/day, 95th 123.2 ng/kg bw/day) were well below far less than the temporary tolerable reference dose of BPA that recommended by the European Food Safety Authority (4 μg/kg bw/day by). The reference level of BPA for healthy population was determined to be 4.09 μg/L via the percentile method.

Antibiotic resistance genes (ARGs) are abundantly shed in feces. Thus, it is crucial to identify their host sources so that ARG pollution can be effectively mitigated and aquatic ecosystems can be properly conserved. Here, spatiotemporal variations and sources of ARGs in the Longjiang watershed of South China were investigated by linking them with microbial source tracker (MST) indicators. The most frequently detected ARGs (>90%) were sulI, sulII, blaTEM, tetW, ermF, and the mobile element intI1. Spatial distribution analyses showed that tributaries contributed significantly more sulI, sulII, and ermF contamination to the Longjiang watershed than the main channel. MST indicator analysis revealed that the Longjiang watershed was contaminated mainly by human fecal pollution. Livestock- and poultry-associated fecal pollution significantly declined after the swine fever outbreak. The occurrence of most ARGs is largely explained by human fecal pollution. In contrast, pig fecal pollution might account for the prevalence of tetO. Moreover, combined human-pig fecal pollution contributed to the observed blaNDM₋₁ distribution in the Longjiang watershed. Subsequent analysis of the characteristics of MST markers disclosed that the relatively lower specificities of BacHum and Rum-2-Bac may lead to inaccurate results of tracking ARG pollution source. The present study determined spatiotemporal variations and ARG origins in the Longjiang watershed by combining MST markers. It also underscored the necessity of using multiple MST markers simultaneously to identify and characterize ARG pollution sources accurately.

Wastewater treatment plants (WWTPs) are considered one of the important sources of aquatic/terrestrial microplastic (MP) pollution. Therefore, the abundance and properties of MPs in the wastewater and sludge of an urban WWTP in Bursa Turkey were investigated. The amount, properties, and removal of MPs were evaluated. The results showed that the average abundance of MPs was 135.3 ± 28.0 n/L in the influent and 8.5 ± 4.7 n/L in the effluent, with a 93.7% removal rate, MP was removed and transferred to the sludge. The daily MP amount released in the aquatic environment is calculated as 525 million MPs, and the annual amount is 1.9 × 10¹¹ MPs. The abundance of MPs in the sludge thickening and sludge filter cake is 17.9 ± 2.3 and 9.5 ± 2.3 n/g dry weight (dw), respectively. The sludge disposal amount of WWTP is 81.5 tons/day and the approximate amount of MP accumulated in the sludge per year is calculated as 2.8 × 10¹¹ MPs. In wastewater and sludge samples, fragment dominant shape, black main colour, and 500–1000 μm sizes are the most common size. The main MP types in wastewater samples at the influent are polypropylene (PP, 36.8%), polyethylene (PE, 31.0%), polystyrene (PS, 11.8%), polyethylene terephthalate (PET, 8.0%), and polyamide (PA, 7.1%), at the effluent (PE, 33.0%), (PP, 52.5%), and (PS, 8.2%). In the sludge cake, the distribution is (PE, 40.8%), (PP, 27.6%), (PS, 18.7%) and (PET, 8.0%). The results of this study show that MPs are removed from wastewater with high efficiency by treatment processes and a significant amount accumulates in the sludge. Therefore, it is suggested that to integrate advanced treatment processes into urban WWTPs and use effective sludge disposal management practices to reduce the amount of MP released into the environment with effluent and sludge.

Mulch film (MF) residues is an important source of microplastics (MPs) in farmland, but its transportation risk to the wider environment was still unknown. Some researches have pursued the sources of MPs found in exorheic rivers. Even so, a systematic study depicting the occurrence, source and fate of microplastics derived from mulch films (MPMF), the crucial component of MPs in farmlands, in exorheic rivers still lacking. Here, the combination of UV–Vis Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) was used to identify the full-size MPMF (1–5000 μm) in field sediment samples collected by single-diagonal systematic sampling. This study verified that MPMF, a polyethylene-matrix composite doped with additives, contributed a considerable part of MPs detected in upstream farmland soil and riverine sediments, and even had an abundance of 38 ± 11 items/kg to 82 ± 15 items/kg, accounting for 9.0%–13.7% of the total MPs in estuary sediments. Notably, upstream farmland was identified to the main source of the riverine MPMF by partial least square path modeling (PLS-PM), contributing to 94.7% of MPMF in riverside sediments and 85.0% of MPMF in estuary sediments. Our study first demonstrates that MPMF constitutes a non-negligible component of MPs in estuarine sediments and underlines the urgency of strengthening the management of MPs pollution in drainage areas with a high agricultural intensity.

Although biochar supports were widely adopted to fabricate the biochar (BC) supported layered double hydroxides (LDHs) composites (LDH-BC) for efficient environmental remediation, few studies focus on the important role of biochar support in alleviating the stacking of LDHs and enhancing LDH-BC's performance. Through the analysis of the material structure-performance relationship, the “support effect” of fine biochar prepared by ball milling was carefully explored. Compared with the original LDHs on LDH-BC, the LDHs on ball milled biochar (LDH-BMBC) had smaller particle size (from 1123 nm to 586 nm), crystallite size (from 20.5 nm to 6.56 nm), more abundant O-containing functional groups, and larger surface area (370 m² g⁻¹) and porous structure. The Langmuir model revealed that the maximum theoretical phosphate adsorption capacity of LDH-BMBC (56.2 mg P g⁻¹) was significantly higher than that of LDH-BC (27.6 mg P g⁻¹). The leaching experiment proved that the addition of LDH-BMBC in calcareous soil could significantly reduce the release of soil total phosphate (46.1%) and molybdate reactive phosphate (40.4%), even though pristine BC and BMBC significantly enhanced the soil phosphate leaching. This work fabricated high-performance and eco-friendly LDH-BMBC for phosphate adsorption in solution and phosphate retention in soil and also provide valuable insights into fine biochar support effect on LDHs exfoliation, extending the practical use of the engineered ball milled biochars in environment remediation.

Paraquat (PQ) is one of the most commonly used herbicides, but it has polluted the environment and threatened human health through extensive and improper usage. Here, a new naked-eye PQ immunochromatographic strip was developed to recognize PQ in domestic water and real human samples within 10 min based on a novel custom-designed anti-PQ antibody. The PQ test strip could recognize PQ at a concentration as low as 10 ng/ml, reaching the high-efficiency time-of-flight mass spectrometry detection level and identifying trace amounts of PQ in samples treated with a diquat (DQ) and PQ mixture. Notably, both the performance evaluation and clinical trial of the proposed PQ strips were validated in multiple hospitals and public health agencies. Taken together, our study firstly provide the clinical PQ-targeted colloidal gold immunochromatographic test strip designed both for environment water and human sample detection with multiple advantages, which are ready for environmental monitoring and clinical practice.

The removal of excessive ammonium from water is vital for preventing eutrophication of surface water and ensuring drinking water safety. Several studies have explored the use of biochar for removing ammonium from water. However, the efficacy of pristine biochar is generally weak, and various biochar modification approaches have been proposed to enhance adsorption capacity. In this study, biochar obtained from giant reed stalks (300, 500, 700 °C) was modified by sulfonation, and the ammonium adsorption capabilities of both giant reed biochars (RBCs) and sulfonated reed biochars (SRBCs) were assessed. The ammonium adsorption rates of SRBCs were much faster than RBCs, with equilibrium times of ∼2 h and ∼8 h for SRBCs and RBCs, respectively. The Langmuir maximum adsorption capacities of SRBCs were 4.20–5.19 mg N/g for SRBCs, significantly greater than RBCs (1.09–1.92 mg N/g). Physical-chemical characterization methods confirmed the increased levels of carboxylic and sulfonic groups on sulfonated biochar. The reaction of ammonium with these O-containing functional groups was the primary mechanism for the enhancement of ammonium adsorption by SRBCs. To conclude, sulfonation significantly improved the adsorption performance of biochar, suggesting its potential application for ammonium mitigation in water.

Iron particles present in drinking water distribution systems (DWDSs) could cause discoloration, while organic pollutants in DWDSs, such as perfluorooctanoic acid (PFOA), could be enriched by iron particles. However, little is known about the enhanced effects of PFOA and iron particles in DWDSs. To fill in these knowledge gaps, herein, iron-PFOA (FEP) particles were generated using residual chlorine as an oxidant in drinking water conditions and then separated into different sizes (ranging from small to large: FEP-S, FEP-M ，and FEP-L). FEP-S harbored the greatest cytotoxicity among the sizes. Interestingly, our data revealed that the PFOA released from FEP particles transformed into PFOS (perfluorooctane sulfonate) upon digestion in the gastrointestinal environment (GI), and FEP-L bored the strongest transformation, showing a toxicity profile that was distinct from that of FEP-S. Furthermore, mechanistic studies revealed that FEP per se should be accountable for the conversion of PFOA to PFOS dependent on the generation of hydroxyl radicals (·OH) in GI, and that FEP-L revealed the greatest production of ·OH. Collectively, these results showed how iron particles and PFOA could result in enhanced toxicity effects in drinking water: (i) PFOA could increase the toxicity of iron particles by reducing particle size and inducing higher generation of ·OH; (ii) iron particles could induce the transformation of PFOA into more toxic PFOS through digestion.

The negative influence of agrochemicals (pesticides: insecticide, fungicide, and herbicide) on biodiversity is a major ecological concern. In recent decades, many insect species are reported to have rapidly declined worldwide, and pesticides, including neonicotinoids and fipronil, are suspected to be partially responsible. In Japan, application of systemic insecticides to nursery boxes in rice paddies is considered to have caused rapid declines in Sympetrum (Odonata: Libellulidae) and other dragonfly and damselfly populations since the 1990s. In addition to the direct lethal effects of pesticides, agrochemicals indirectly affect Odonata populations through reductions in macrophytes, which provide a habitat, and prey organisms. Due to technical restrictions, most previous studies first selected target chemicals and then analyzed their influence on focal organisms at various levels, from the laboratory to the field. However, in natural and agricultural environments, various chemicals co-occur and can act synergistically. Under such circumstances, targeted analyses might lead to spurious correlations between a target chemical and the abundance of organisms. To address such problems, in this study we adopted a novel technique, “Comprehensive Target Analysis with an Automated Identification and Quantification System (CTA-AIQS)” to detect wide range of agrochemicals in water environment. The relationships between a wide range of pesticides and lentic Odonata communities were surveyed in agricultural and non-agricultural areas in Saga Plain, Kyushu, Japan. We detected significant negative relationships between several insecticides, i.e., acephate, clothianidin, dinotefuran, flubendiamide, pymetrozine, and thiametoxam (marginal for benthic odonates) and the abundance of lentic Epiprocta and benthic Odonates. In contrast, the herbicides we detected were not significantly related to the abundance of aquatic macrophytes, suggesting a lower impact of herbicides on aquatic vegetation at the field level. These results highlight the need for further assessments of the influence of non-neonicotinoid insecticides on aquatic organisms.