The emission of mercury (Hg) from cropland soil greatly affects the global Hg cycle. Combinations of different crop cultivars and planting densities will result in different light transmittance under canopies, which directly affects the solar and heat radiation flux received by the soil surface below crops. In turn, this might lead to differences in the soil–air total gaseous mercury (TGM) exchange under different cropping patterns. However, soil–air TGM exchange fluxes in croplands under differing canopies have been poorly investigated. Here, a one-year observation of TGM exchange flux was conducted for cropland soils covering five different crop cultivars and three planting densities in North China Plain using the dynamic flux chamber method. The results showed that light transmittance under the canopies was the key control on soil–air TGM exchange fluxes. High light transmittance can enhance soil TGM emission rates and increase the magnitude of diurnal variations in soil–air TGM exchange fluxes. Furthermore, we found that there were piecewise–function relationships (Peak function–constant equation) between light transmittance under the different canopies and the numbers of days after crop sowing. The soil–air TGM exchange fluxes showed a parabolic response to changes in light transmittance under the different canopies. A second-order model was established for the response relationship between soil–air TGM exchange flux and soil Hg concentration, total solar radiation above the canopy, and numbers of days after sowing. The estimated annual average soil–air TGM exchange flux was 5.46 ± 21.69 ng m⁻² h⁻¹ at corn–wheat rotation cropland with 30 cm row spacing using this second-order model. Our results might a data reference and a promising foundation for future model development of soil–air TGM exchange in croplands under different crop cultivars and planting densities.

Next to the city of Huelva (SW of Spain), around 100 Mt of phosphogypsum (PG) are stored in stacks on the salt-marshes of the Tinto River estuary covering a surface of about 1000 ha. Due to the high content of ²³⁸U series natural radionuclides of the PG, its acidic nature (pH about 3), and the fact that PG stacks were disposed without any kind of isolation from the substrate, they could produce a potential radioactive impact into the underlying sediments.The aim of this work is to assess the pollution of the underlying sediments by natural radionuclides coming from the PG stacks. To this end, seven cores were taken, and PG and sediments samples collected at different depths were analysed. The activity concentrations of the main long half-live natural radionuclides of interest were determined by applying both gamma-ray and alpha-particle spectrometry radiometric techniques.The results of this study showed that the first decimeters of salt-marsh sediment act as a “barrier” for the radionuclides coming from the PG stacks decreasing rapidly its activity concentration in depth, affecting mainly sediments located in the first 20 cm below the contact due to mixing processes. While ²³⁰Th, ²²⁶Ra and ²¹⁰Pb pollution is mainly restricted to the first 20 cm of sediments, U-isotopes can reach higher depths (up to around 50 cm) by leaching processes due to their lower reactivity and higher concentration in the polluted leachates. The obtained results have high relevance for the design of the perimeter channel which is projected to build in the restoration project, suggesting that should has around 1 m deep under the base of the PG stacks, to ensure the full collection of polluting leachates, and to prevent their release into the estuary of the Tinto River.

Herein, a new peroxymonosulfate (PMS) activation system was established using a biochar (BC)-supported Co₃O₄ composite (Co₃O₄-BC) as a catalyst to enhance chloramphenicols degradation. The effects of the amount of Co₃O₄ load on the BC, Co₃O₄-BC amount, PMS dose and solution pH on the degradation of chloramphenicol (CAP) were investigated. The results showed that the BC support could well disperse Co₃O₄ particles. The degradation of CAP (30 mg/L) was enhanced in the Co₃O₄-BC/PMS system with the apparent degradation rate constant increased to 5.1, 19.4 and 7.2 times of that in the Co₃O₄/PMS, BC/PMS and PMS-alone control systems, respectively. Nearly complete removal of CAP was achieved in the Co₃O₄-BC/PMS system under the optimum conditions of 10 wt% Co₃O₄ loading on BC, 0.2 g/L Co₃O₄-BC, 10 mM PMS and pH 7 within 10 min. The Co₃O₄/BC composites had a synergistic effect on the catalytic activity possibly because the conducting BC promoted electron transfer between the Co species and HSO₅⁻ and thus accelerated the Co³⁺/Co²⁺redox cycle. Additionally, over 85.0 ± 1.5% of CAP was still removed in the 10th run. Although both SO₄⁻ and OH were identified as the main active species, SO₄⁻ played a dominant role in CAP degradation. In addition, two other chloramphenicols, i.e., florfenicol (FF) and thiamphenicol (TAP), were also effectively degraded with percentages of 86.4 ± 1.3% and 71.8 ± 1.0%, respectively. This study provides a promising catalyst Co₃O₄-BC to activate PMS for efficient and persistent antibiotics degradation.

The co-contamination of arsenic (As) and cadmium (Cd) in soils is a common problem. Selenium (Se) can reduce the uptake of As and Cd in plants, and in practice, the alternate wetting and drying is a common culture mode in rice production. However, it is unknown whether Se can efficiently reduce As and Cd concentrations in crops suffering from a high-level contamination of As and Cd under different soil water conditions. In this study, we assessed the efficiency and risks of selenite [Se(IV)], in a pot experiment, to reduce the uptake of As and Cd in a rice plant (YangDao No 6) growing in a heavily contaminated soil by As and Cd (pH 7.28) under different soil water conditions. The results showed that Se(IV) failed to control the grain total As and Cd concentrations within their individual limited standard (0.2 mg kg⁻¹) despite that Se(IV) significantly reduced the grain total As and Cd concentrations. The soil drying treatment alone could reduce the accumulation of arsenite [As(III)] in the grains, but additional Se(IV) stimulated the accumulation of As(III) in the grains under soil drying conditions. In addition, the addition of Se(IV) enhanced the As and Cd concentrations in the shoots and/or roots of rice plants under certain conditions. The above results all suggested that the utilization of Se(IV) in a high contaminated soil by As and Cd cannot well control the total concentrations of As and Cd in plants. In this study, the available concentrations of As and Cd in the rhizosphere soil, the rhizosphere soil pH, the formation of root iron/manganese plaques and the concentrations of essential elements in the grains were monitored, and the related mechanisms on the changes of these parameters were also discussed. This study will give a guideline for the safe production of rice plants in a heavily co-contaminated soil by As and Cd.

Microplastics are widespread across the global oceans, yet the potential risks of the ubiquitous environmental contaminant to marine organisms has been less known. Accumulation of microplastics and associated contaminants in marine fish, may pose adverse impacts to human health via seafood consumption. This study evaluated microplastic contamination in 24 fish species collected from Beibu Gulf, one of the world’s largest fishing grounds in South China Sea. Microplastics were detected in 12 fish species at an abundance of 0.027–1.000 items individual⁻¹ and found in fish stomach, intestines and gills with the count percentage of 57.7%, 34.6% and 7.7%, respectively. Transparent fibers were observed as the predominant microplastics, which might be ingested accidently by fish or transferred through other animals at lower trophic levels. Majority of microplastics were identified as polyester (44%) and nylon (38%), whereas polypropylene (6%), polyethylene (6%), and acrylics (6%) were also found. Relatively, higher microplastic abundances were found in demersal fish compared to the pelagic species. Overall, the abundance of microplastics was documented as relatively low in the commercial fish collected from the open water of Beibu Gulf, South China Sea.

The strict environmental management has been implemented in Taihu Basin to reduce the surface water contamination; however, the effectiveness of the management actions has not been comprehensively evaluated. In the present study, 364 samples were collected during four campaigns over a span of one year from surface water, municipal wastewater treatment plants (MWWTPs), industrial wastewater treatment plants (IWWTPs), industrial enterprises, and aquaculture in a typical region in the Upper Taihu Basin. Overall concentration, temporal variation and spatial distribution of 16 PAHs in surface water and various pollution sources were evaluated and the potential pollution sources were identified. Results showed that concentrations of individual PAHs in the surface water ranged from less than the limit of quantification (LOQ) to 949 ng L⁻¹, indicating a reduction of PAH contamination level after the implementation of environmental management actions. Influent of MWWTPs and wastewater from industrial enterprises exhibited relatively high ∑PAHs concentrations (mean: 880 ng L⁻¹ and 642 ng L⁻¹, respectively); these samples also exhibited a similar seasonal variation as well as composition of PAH congeners to those found in surface water, and therefore were designated as the main emission sources of PAHs in the studied region. Additional source apportionment using principal component analysis was also conducted to verify the proposed sources and diagnose other pollution sources. The findings provided a thorough understanding of PAH pollution, especially its major emission sources, in a typical region with pollution-intensive industries after the implementation of strict environmental management.

This work aimed at predicting the toxic effects of phenolic compounds in Ba River on the health of female sharpbelly (Hemiculter lucidus) by the de novo transcriptomic analysis of the liver. Sharpbelly, a native fish living in freshwater ecosystem of East Asia, were sampled upstream, near, and downstream of a wastewater discharge to the Ba river. Based on the occurrence of bisphenol A (BPA), nonylphenol (NP), and 4-tert-octylphenol (4-t-OP) in the water and fish sampled from each site, up-, mid-, and down-stream were interpreted as control, high, and low treatment groups, respectively. In the mid-stream group the Fulton’s condition factor (CF) and body weight were remarkably increased by approximate 20%; the gonado-somatic index (GSI) and hepatosomatic index (HSI) in mid-stream fish showed a similar increasing trend but lacking of statistical difference. Exposure to wastewater effluent caused 160 and 162 differentially expressed genes (DEGs) in up-mid and down-mid stream groups, respectively. Two sets of DEGs were primarily enriched in the signaling pathways of drug metabolism, endocrine system, cellular process, and lipid metabolism in the mid-stream sharpbelly, which may alter the fish behavior, disrupt the reproductive function, and lead to hypothyroidism, hepatic steatosis, etc. Taken together, our results linked the disrupted signaling pathways with activities of phenolic compounds to predict the potential effects of wastewater effluent on the health of wild fish.

Particulate matter (PM) pollution is a serious environmental problem in most of the cities in the Yangtze River Delta region. Plants can effectively filter ambient air by adsorbing PM. However, only a few studies have paid attention to the dynamic changes and seasonal differences in particle retention capacities of plants under long-term pollution. In this study, we investigated the dynamic changes in particle retention capabilities of the evergreen, broad-leaved, greening plants—Euonymus japonicus var. aurea-marginatus and Pittosporum tobira—in spring and summer. We employed an open-top chamber to simulate the severity of the tail gas pollution. The results showed that, both the plants reached a saturated state in 18–21 days, under continuous exposure to pollution (daily concentration of PM₂.₅: 214.64 ± 321.33 μg·cm⁻³). This was 6–8 days longer than that in the field experiments. In spring, the maximum retention of total particulate matter per unit leaf area of E. japonicus var. aurea-marginatus and P. tobira was 188.47 ± 3.72 μg cm⁻² (18 days) and 67.63 ± 2.86 μg cm⁻² (21 days), respectively. In summer, E. japonicus var. aurea-marginatus and P. tobira reached the maximum retention of the particle on the 21st day, with a net increase of 94.10 ± 3.77 μg cm⁻² and 27.81 ± 3.57 μg cm⁻², respectively. Irrespective of season, the particle retention capacity of E. japonicus var. aurea-marginatus was higher than that of P. tobira, and it showed a better effect on reducing the concentration of fine particles in the atmosphere. The particle retention of the two plants was higher in spring than that in summer. E. japonicus var. aurea-marginatus displayed a significant difference in particle retention between the seasons, while P. tobira did not show much difference. These results will provide a foundation for future studies on the dynamic changes and mechanism of particle retention in plants and management practices by employing plants for particle retention in severely polluted areas.

The automatic identification (location, segmentation, and classification) by UAV- based optical imaging of spills of transparent floating Hazardous and Noxious Substances (HNS) benefits the on-site response to spill incidents, but it is also challenging. With a focus on the on-site optical imaging of HNS, this study explores the potential of single spectral imaging for HNS identification using the Faster R-CNN architecture. Images at 365 nm (narrow UV band), blue channel images (visible broadband of ∼400–600 nm), and RGB images of typical HNS (benzene, xylene, and palm oil) in different scenarios were studied with and without Faster R-CNN. Faster R-CNN was applied to locate and classify the HNS spills. The segmentation using Faster R-CNN-based methods and the original masking methods, including Otsu, Max entropy, and the local fuzzy thresholding method (LFTM), were investigated to explore the optimal wavelength and corresponding image processing method for the optical imaging of HNS. We also compared the classification and segmentation results of this study with our previously published studies on multispectral and whole spectral images. The results demonstrated that single spectral UV imaging at 365 nm combined with Faster R-CNN has great potential for the automatic identification of transparent HNS floating on the surface of the water. RGB images and images using Faster R-CNN in the blue channel are capable of HNS segmentation.

The optical properties of light-absorbing carbonaceous aerosols have caused increasing concerns due to their significant impacts on local and regional climates. In this study, particles from biomass burning in home stoves were collected and evaluated for their optical properties. The absorption Ångström exponent (AAE) values ranged from 1.17 to 2.92 and negatively correlated with the modified combustion efficiency, indicatinging more brown carbon in combustion emissions with relatively low combustion efficiencies. The average contribution of brown carbon to the total aerosol absorption at 370 nm was equally as important as that of black carbon (BC), with the average relative contribution fraction of 50% varying from 10% to 84% for different biomasses. The average value of the mass absorption efficiency (MAE) of BC (MAEBC) at 880 nm was positively correlated with the ratio of organic carbon to elemental carbon, indicating the significant coating effects of organic aerosols. The MAE values of BrC at 370 nm were in the range of 1.1–11.3 m²/g, with an average of 5.1 ± 2.2 m²/g. The estimated absorption emission factors at 370 nm and 880 nm were 3.75 ± 3.45 and 0.84 ± 0.78 m²/kg, respectively. Optical property information of particles emitted from real-world biomass burning are imperative in future modeling studies of biomass burning impacts on climate. The limitation of the relatively small sample size for each subgroup fuel calls for more field- and lab-based emission characterization research.