The principal aim of this study was to understand the enrichment patterns of elements in water from typical coal mine and irrigation areas. For this study, samples of surface water, shallow water, and deep water were collected from Handan, Jining, and Heze cities and their surrounding areas in the central North China Plain. The results showed that the hydrochemical characteristics were dominated by Ca–Mg–Cl and Ca–HCO₃. Elements in the studied surface water, including strontium, iron and boron, were anomalously enriched at levels more than 654, 294 and 134 times their global river water averages, respectively. The concentrations of elements in the studied area were influenced by both natural processes and anthropogenic sources, but the dominant origins of the anomalous enriched elements were bedrock weathering and soil leaching. The deep well water quality in the Handan coal mining area was good, while the poor-quality water samples in the study area were mainly distributed in the alluvial plain, which is characterized by Neogene-Quaternary sediments and aquifers. The measured hazard quotient and hazard index values indicate that the arsenic and nickel in the studied samples could pose a noncarcinogenic risk to the health of local residents, especially children. The leading source of the high arsenic levels is influenced by natural process. Monitoring plans for arsenic, iron, manganese, nitrate and other potentially harmful elements in surface water and groundwater and effective health education on pollution by these elements are essential.

The effects of the continuous accumulation of Zinc (Zn) on the fate of antibiotic resistance genes (ARGs) in constructed wetland-microbial fuel cells (CW-MFCs) remain unclear. In this study, the impacts of Zn addition and a circuit mode on antibiotic removal, occurrence of ARGs, the bacterial community, and bacterial functions were investigated in three groups of CW-MFCs. The results showed that continuous Zn exposure enriched the target ARGs during the initial stage, while excessive Zn accumulation decreased antibiotic removal and the abundance of ARGs. A principal component analysis demonstrated that ARGs and the bacterial community distribution characteristics were significantly impacted by the mass accumulation of antibiotics and Zn, as well as the circuit mode. A redundancy analysis, partial least squares path modeling, and Procrustes analysis revealed that the accumulation of antibiotics and Zn, the composition of the bacterial community, the circuit mode, and the abundance of intI associated with horizontal gene transfer jointly contributed to the distributions of ARGs in the electrodes and effluent. Moreover, continuous exposure to Zn decreased the bacterial diversity and changed the composition and function of the bacterial community predicted using PICRUSt tool. The co-occurrence of ARGs, their potential hosts and bacterial functions were further revealed using a network analysis. A variation partition analysis also showed that the accumulation of target pollutants and the circuit mode had a significant impact on the bacterial community composition and functions. Therefore, the interaction among ARGs, the bacterial community, bacterial functions, and pollutant accumulations in the CW-MFC was complex. This study provides useful implications for the application of CW-MFCs for the treatment of wastewater contaminated with antibiotics and heavy metals.

Soil application of Zn fertilizer is an effective approach to improve yield and Zn accumulation in wheat grain. However, it remains unclear whether repeated Zn application can result in high accumulation of heavy metals (HMs) in soils and grains and thus represents a potential risk for human consumption. This study aimed to evaluate the health risk assessment of HMs in a wheat production system which had continuously received 8 years of Zn application at varying rates (0, 2.3, 5.7, 11.4, 22.7, 34.1 kg Zn ha⁻¹). The results showed that Zn application significantly increased the soil total Zn concentration without affecting concentrations of As, Pb, Cd, Cu and Cr. Across Zn rates, Zn application increased grain concentrations of Zn, Pb and Cd by 75%, 51% and 14%, respectively, and reduced grain As concentration by 14%. The human health risk assessment revealed that the threshold hazard quotients for the individual HM were below 1, independent of Zn rates. The hazard index (HI) values at Zn rates of 11.4, 22.7 and 34.1 kg Zn ha⁻¹ were significantly greater than that at null Zn treatment. Furthermore, exposures to As, Cu and Zn accounted for 97% of HI at all Zn rates. Analysis of the threshold cancer risk with Pb and As showed that ingestion of wheat grain even from highest Zn application rate wouldn’t bring the lifetime carcinogenic risk. In contrast, long-term Zn application significantly reduced the carcinogenic risk of As by 9.7–26.5%. In conclusion, repeated soil applications of Zn at optimal rate (5.7 kg Zn ha⁻¹) didn’t cause health risk for Zn, Cu, Cd, Pb, Cr, and As, while improving productivity and grain Zn concentration of wheat to meet human recruitment. Our study highlights the importance of appropriate Zn fertilizer management in improving grain quality while reducing HMs risks from human consumption.

A few experimental studies suggest that atmospheric pollutants could affect the endocrine system, and in particular stress hormones and the hypothalamic-hypophyseal-ovarian axis, which could in turn influence menstrual cycle function. We aimed to study the possible short-term effects of atmospheric pollutants on the length of the follicular and luteal phases and on the duration of the menstrual cycle in humans. To do so, from a nation-wide study on couples’ fecundity, we recruited 184 women not using contraception who collected urine samples at least every other day during one menstrual cycle, from which a progesterone metabolite was assayed, allowing estimation of the duration of the follicular and luteal phases of the cycle. Atmospheric pollution (nitrogen dioxide and particulate matter with an aerodynamical diameter below 10 μm, PM₁₀) levels were estimated from a dispersion model with a 1-km resolution combined with permanent monitoring stations measurements, allowing to estimate exposures in the 30-day, 1–10 and 11-30-day periods before the start of the menstrual cycle. Regression models allowed to quantify the change in cycle duration associated with atmospheric pollutants and adjusted for potential confounders. Follicular phase duration increased on average by 0.7 day (95% confidence interval, CI, 0.2; 1.3) for each increase by 10 μg/m³ in NO₂ concentration averaged over the 30 days before the cycle and by 1.6 day (95% CI, 0.3; 2.9) for each increase by 10 μg/m³ in PM₁₀. There was no strong evidence of associations of exposures in this time window with luteal phase or with total menstrual cycle durations (p > 0.2). Exposures in the 1–10 day period before the cycle start were also associated with increased follicular phase duration. This study is one of the first prospective studies to suggest short-term alterations in follicular phase duration following atmospheric pollutants exposure.

The Bohai Sea is a shallow-water, semi-enclosed marginal sea of the Northwest Pacific. Since the late 1990s, it has suffered from nutrient over-enrichment. To better understand the eutrophication characteristics of this important coastal sea, we examined four survey datasets from summer (June 2011), late autumn (November 2011), winter (January 2016), and early spring (April 2018). Nutrient conditions in the Bohai Sea were subject to seasonal and regional variations. Survey-averaged N/P ratios in estuarine and nearshore areas were 20–133. In contrast, the central Bohai Sea had mean N/P ratios of 16.9 ± 3.4 in late autumn, 16.1 ± 3.0 in winter and 13.5 ± 5.8 in early spring, which are close to the traditional N:P Redfield ratio of 16. In summer, both dissolved inorganic nitrogen (DIN) and dissolved inorganic phosphate (DIP) were used up in the surface waters of the central Bohai Sea, suggesting that the biological consumption of DIN and DIP may also follow the Redfield ratio. Wintertime nutrient budgets of the central Bohai Sea water were then established based on a mass balance study. Our results suggest that the adjacent North Yellow Sea supplied additional DIP to the central Bohai Sea via wintertime water intrusion, balancing terrigenous excess DIN that was introduced in summer. A water-mixing simulation combining these two nutrient sources with atmospheric nitrogen deposition suggests that eutrophication in the central Bohai Sea will likely be enhanced by the large-scale accumulation of anthropogenic nitrogen in adjacent open oceans. Such changes in nutrients may have fundamentally contributed to the recent development of algal blooms and seasonal hypoxia in the central Bohai Sea.

Vehicle emissions are a major contributor to air pollution in China. In this study, a high-resolution inventory of eight on-road vehicle-emitted pollutants in 53 cities within the North China Plain (NCP) was established for 152 sub-sources. Monthly emission factors were then simulated using the COPERT v5 model and their spatial distribution at 4 km × 4 km resolution was allocated based on the transportation network. In 2017, emissions of BC, CO, NH₃, NMVOCs, NOₓ, PM₁₀, PM₂.₅, and SO₂ were 38.3, 2900, 21.8, 578, 2460, 113, 85.9, and 4.7 kt, respectively. These emissions and their sources differed between cities, mainly due to different vehicle populations, fleet compositions, emission share rates of different vehicle types, and emission standards in each city. Small-medium petrol passenger cars and both 20–26 t and 40–50 t heavy-duty diesel trucks of China 3 and 4 emissions standards were the main contributors for all pollutants. Higher cold-start emission factors caused higher emissions of CO, NMVOCs, NOₓ, and PM₂.₅ in winter. The cities of Beijing, Zhengzhou, Tianjin, Tangshan, Xuzhou, Qingdao, Jinan, Jining, and Zibo had the highest emission intensities. Overall, emissions decreased from the city centers toward surrounding areas. The higher contributions of heavy-duty trucks meant that higher emissions appeared along highways in a vein-like distribution. These results provide a theoretical basis for the effective prevention and control of air pollution in the NCP.

As emerging pollutants, the occurrence and risks of organophosphate esters (OPEs) in mariculture farms should be concerned; however, information is limited. Beibu Gulf is one of the essential mariculture zones in China. This study aimed to investigate the occurrence of OPEs in mariculture farms of the Beibu Gulf, their phase distribution and bioaccumulation among sediment, organisms (shrimp, crab, and oyster), water, and feed. Human exposure to OPEs through seafood consumption was also assessed. The total concentrations of the 11 target OPEs (∑₁₁OPEs) in the water samples ranged 32.9–227 ng L⁻¹. It was significantly higher in water from the culture ponds (mean 122 ng L⁻¹) than in water from the estuaries and nearshore areas (mean 51.1 ng L⁻¹) (nonparametric test, p < 0.05). ∑₁₁OPEs in the feeds averaged 46.0 (range 21.7–84.5) ng g⁻¹ dw, which is similar to the level in the organism samples (mean 55.5, range 21.3–138 ng g⁻¹ dw) and 4.4 times higher than that in the sediment (mean 10.9, range 35–22.1 ng g⁻¹ dw). The ∑₁₁OPEs released from the feeds to the culture ponds was estimated to be 49 μg m⁻² per three-month period. In the aquaculture ponds, the sediment-water distribution coefficient (log KOC), and the bioaccumulation factors from the water (log BWAFs) or the feed (log BFAFs) to the organisms, depend linearly on the hydrophobicity (log KOW) of OPEs. The log BWAFs and log BFAFs increased with increasing log KOW within the log KOW range of 1–7. The human exposure to OPEs through consumption of shrimp, crab, and oysters from the mariculture farms does not pose a health risk at present.

The imprudent agricultural practices are leading to an increasing load of pesticides in agricultural fields. Thus, there is a need to minimize the harmful effect of pesticides by adopting sustainable strategies. In the recent past decade, kinetin, a plant synthetic hormone, has been reported as a pesticide toxicity alleviator in higher plants. But its role in mitigating pesticide toxicity in cyanobacteria is still limited. Thus, in current study an attempt has been made to investigate the potential of kinetin in regulating cypermethrin, an insecticide, induced toxicity in Anabaena PCC 7120 and Nostoc muscorum ATCC 27893. Cypermethrin (Cyp₁; 2 μg ml⁻¹ and Cyp₂; 4 μg ml⁻¹) showed negative impact on growth, photosynthetic pigments, photosynthetic O₂-evolution and primary photochemistry of PS II (Phi_P₀, Psi_₀, Phi_E₀) resulting in decrease in performance index (PIABS). However, under similar conditions, increases in energy flux parameters (ABS/RC, TR₀/RC, ET₀/RC and DI₀/RC) were noticed. Cypermethrin at both the doses enhanced the level of oxidative stress biomarkers (SOR, H₂O₂, and MDA equivalent contents) despite of increased antioxidant enzymatic activity (SOD, POD, CAT and GST).Under similar condition, cypermethrin at tested doses caused substantial decrease in non-enzymatic antioxidant contents (proline, cysteine and NP-SH). Nevertheless, kinetin treatment attenuated cypermethrin induced oxidative stress by further up-regulating the activity of enzymatic antioxidants and by enhancing the contents of non-enzymatic antioxidants. Thus, with the application of kinetin improved photochemistry of PS II and growth yield of both the cyanobacteria were observed even in the presence of cypermethrin. Current results establish that cypermethrin induces toxicity on photosynthesis, photosynthetic pigments and growth, and this effect was more pronounced in Anabaena PCC 7120 than Nostoc muscorum ATCC 27893. Furthermore, the potential role of kinetin in mitigating the toxicity of cypermethrin in both the cyanobacteria provides an insight to be used in paddy fields for sustainable agricultural practices.

This study investigates the influence of meteorology, land use, built environment, and traffic characteristics on near-road ultrafine particle (UFP) concentrations. To achieve this objective, minute-level UFP concentrations were measured at various locations along a major arterial road in the Greater Toronto Area (GTA) between February and May 2019. Each location was visited five times, at least once in the morning, mid-day, and afternoon. Each visit lasted for 30 min, resulting in 2.5 h of minute-level data collected at each location. Local traffic information, including vehicle class and turning movements, were processed using computer vision techniques. The number of fast-food restaurants, cafes, trees, traffic signals, and building footprint, were found to have positive impacts on the mean UFP, while distance to the closest major road was negatively associated with UFP. We employed the Extreme Gradient Boosting (XGBoost) method to develop prediction models for UFP concentrations. The Shapley additive explanation (SHAP) measures were used to capture the influence of each feature on model output. The model results demonstrated that minute-level counts of local traffic from different directions had significant impacts on near-road UFP concentrations, model performance was robust under random cross-validation as coefficients of determination (R²) ranged from 0.63 to 0.69, but it revealed weaknesses when data at specific locations were eliminated from the training dataset. This result indicates that proper cross-validation techniques should be developed to better evaluate machine learning models for air quality predictions.

Cigarette butts (CBs) are the most common littered items in the environment and may contain high amounts of polycyclic aromatic hydrocarbons (PAHs) from incomplete tobacco leave burning. The potential relevance of PAHs stemming from CBs for aquatic systems remain unclear since to date there is no systematic study on PAHs leaching from CBs. Therefore, in this study the leaching concentrations of 16 EPA-PAHs (except benzo(ghi)perylene) in 3 different types of water were measured. The concentrations of ΣPAHs leachates from 4 h to 21 days ranged from 3.9 to 5.7, 3.3–5.5, and 3.0–5.0 μg L⁻¹ for deionized, tap, and river waters, respectively. For all contact times, there were no substantial differences of the leachate concentrations of PAHs among different water types. Lighter PAHs had the highest concentrations among the detected PAHs and they were detected in the leachates already after 4 h. Concentrations of indeno(1,2,3-cd)pyrene, and dibenz(a,h)anthracene were below the limit of detection in all water samples at different contact times. At all contact times naphthalene and fluorene had the highest concentrations among the studied PAHs. Tap and river water samples with addition of sodium azide as chemical preservative contained significantly higher concentration of ΣPAHs. Our leaching data showed that leached concentrations of PAHs exceeded the Water Framework Directive (WFD) standards and considering the number of CBs annually littered this may pose a risk to aquatic organisms and potentially also humans.