Microplastic (MP) pollution in the environment has aroused great concern. However, our knowledge of MP abundance and distribution in soil environment is scarce. This work investigated the MPs in the farmland and grassland at a remote area of China, namely, the eastern area of the Qinghai–Tibet Plateau (QTP). The average numbers of MPs were 53.2 ± 29.7 and 43.9 ± 22.3 items/kg in shallow and deep soil, respectively, from 35 soil samples. A remarkable difference in MP abundances was observed among soil samples from mulch farmland, greenhouses, farmland without covering, and grassland. The MPs were mostly in the form of a film and transparent in color in this study. The dominant polymers of MPs in the soil samples were polyester (PE) and polypropylene (PP). This study revealed the characteristics of MP distribution among different land use at the QTP, and MPs may stem from the fragmentation of plastic mulch in farmland soil. Notably, MP abundance increased with the increase in mulching time in facility agriculture. Additionally, human disturbances and increased mulching time in facility agriculture promote the fragmentation of soil MPs. This study provides important data for follow-up research on MPs in a plateau terrestrial ecosystem.

Coastal harmful algal blooms (HABs) in China’s seas have attracted researchers’ attention for decades. Among the four seas of China, the HAB frequency is the highest in the East China Sea (ECS). The impact of climate change and anthropogenic dominant factors on HABs is not well quantified and the response of HABs to the changing climate is also not clear. Here, we compiled a time series of observation-based HAB events since the 1980s and performed a regional assessment to elucidate the dominant drivers of HAB events in the ECS. The results showed that the increase in the frequency of HAB events in the ECS between 2000 and 2003 was associated with increases in dissolved inorganic phosphorus and sea surface temperature anomalies as well as decreasing summer precipitation. The declining annual frequency in HAB events in the ECS after 2003 was associated with the two climatological factors, most notably, precipitation. Under the “business-as-usual” scenario, climate change will increase the annual HAB events in the ECS from the historical frequency (1985–2013) by more than five-fold by the end of 21st century. These findings demonstrated that management strategies based on reducing nutrient loading also need to consider the effects of climate change in the future.

The emissions of tyre wear particles (TWPs) into the environment are increasing and have negative impacts on the environment and human health. The aim of this study was therefore to establish a mass balance for vehicle tyres und TWP emissions in Austria using static material flow analysis, which enabled a quantification of mass flows of rubber including carbon black as the most mass-relevant tyre filler. Vehicle-specific and mileage-dependent emission factors were used to calculate the TWP emissions. The results for the year 2018 indicate that 80% of the tyre rubber remained in use, while 14% was re-treaded, recycled, incinerated or exported as end-of-life tyres and 6% was emitted as TWPs to air, soil or surface water. Of these 21,200 t/y released and dissipative lost TWPs, 6% were microscale, with a possible size between 0.1 and 10 μm, and 0.3% were nanoscale below 0.1 μm. The mass balance on the substance level shows that the TWPs contained 5,500 t/y of carbon black emitted in the form of airborne TWPs (6%) or entering in the soil or surface waters (47% each). Regarding air pollution from road vehicles, about 3,600 t/y were non-exhaust emissions, including tyre, brake and road-surface wear, which contributed to 9% of total dust emissions across Austria. Scenario analysis for 2050 with regard to e-mobility and the European Green Deal reveals that non-exhaust emissions can only be significantly reduced by a general reduction of the mileage or an environmentally friendly tyre design. This modelling approach provides a solid basis for decision makers in traffic planning as well as for chemical risk assessment. However, dynamic models with higher temporal and spatial resolution are needed to predict future mass flows of TWPs and their environmental fate, including their degradation products and possible accumulation effects.

General population are concurrently and extensively exposed to many volatile organic compounds (VOCs), including some Group 1 human carcinogens, such as 1,3-butadiene. However, only a few studies assessed internal exposure levels of VOCs; particularly, very limited studies have examined associations between the urinary concentrations of multiple VOC metabolites (mVOCs) and oxidative stress biomarkers (OSBs) among the general population. In this study, 21 mVOCs and three OSBs including 8-hydroxy-2′-deoxyguanosine (8-OHdG; for DNA), 8-hydroxyguanosine (8-OHG; for RNA), and 4-hydroxy nonenal mercapturic acid (HNEMA; for lipid) were measured in 406 urine samples collected from 128 healthy adults during autumn and winter of 2018 in Wuhan, central China, including repeated samples taken in 3 d from 75 volunteers. Inter-day reproducibility for most mVOCs was good to excellent; urinary concentrations of mVOCs in winter were generally higher than those in autumn. Risk assessment was conducted by calculating hazard quotients for the parent compounds, and the results suggested that acrolein, 1,3-butadiene, and cyanide should be considered as high-priority hazardous ones for management. After false-discovery adjustment, 16 of the studied mVOCs were positively associated with 8-OHdG and 8-OHG (β values ranged from 0.04 to 0.48), and four mVOCs were positively associated with HNEMA (β values ranged from 0.21 to 0.78). Weighted quantile sum regression analyses were used to assess associations of mVOC mixture and OSBs, and we found significantly positive associations between the mixture index and OSBs, among which the strongest mVOC contributors for the associations were 2-methylhippuric acid for both DNA (20%) and RNA (17%) oxidative damage, and trans,trans-muconic acid (50%) for lipid peroxidation. This study firstly reported good to excellent short-term reproducibility, seasonal difference in autumn and winter, and possible health risk in urinary concentrations of multiple mVOCs among the general population.

Vast areas of Europe were contaminated by the fallout of ¹³⁷Cs and other radionuclides, as a result of the Chernobyl accident in 1986. The post-fallout redistribution of Chernobyl-derived ¹³⁷Cs was associated with erosion and sediment transport processes within the fluvial system. Bottom sediments from lakes and reservoirs can provide a valuable source of information regarding the post-fallout redistribution and fate of ¹³⁷Cs released by the Chernobyl accident. A detailed investigation of sediment-associated ¹³⁷Cs in the bottom sediments of a reservoir in a Chernobyl-affected area in Central Russia has been undertaken. A new approach, based on the vertical distribution of ¹³⁷Cs activity concentrations in the reservoir bottom sediment makes it possible to separate the initially deposited bottom sediment, where the ¹³⁷Cs activity reflects the direct fallout of Chernobyl-derived ¹³⁷Cs to the reservoir surface and its subsequent incorporation into sediment deposited immediately after the accident, from the sediment mobilized from the catchment deposited subsequently. The deposits representing direct fallout from the atmosphere was termed the “Chernobyl peak”. Its shape can be described by a diffusion equation and it can be distinguished from the remaining catchment-derived ¹³⁷Cs associated with sediment accumulated with sediments during the post-Chernobyl period. The ¹³⁷Cs depth distribution above the "Chernobyl peak" was used to provide a record of changes in the concentration of sediment-associated ¹³⁷Cs transported from the upstream catchment during the post-Chernobyl period. It was found that the ¹³⁷Cs activity concentration in the sediment deposited in the reservoir progressively decreased during the 30-year period after the accident due to a reduction in the contribution of sediment eroded from the arable land in the catchment. This reflects a reduction in both the area of cultivated land area and the reduced incidence of surface runoff from the slopes during spring snowmelt due to climate warming.

Trace organic compounds (TOrCs) and microplastics (MPs) have been recognized as emerging pollutants that cause severe water pollution related problems due to their non-degradable and bio-accumulative nature. Many studies on oxidation processes such as ozone have been conducted to efficiently remove TOrCs in water treatment. However, there has been a lack of research on the removal efficiency of TOrCs in the oxidation process when they co-exist with MPs and form transformation byproducts (TBPs) during this process. This study evaluates the effects of MPs on TOrC removal during ozonation at various ozone concentrations and based on the mass of MP particles in distilled water. The adsorption of TBPs and TOrCs was also evaluated using the Freundlich and Langmuir isotherm equations. The toxicity of these compounds was evaluated to confirm the risk to aquatic ecosystems. The results show that triclosan (TCS) had the highest absorption capacity amongst the TOrCs and TBPs tested. Polyvinylchloride exhibited the highest adsorption efficiency compared with polyethylene and polyethyleneterephthalate (TCS 0.341 mg/g) due to its high adsorption capacity and hydrophobicity. In the toxicity test, 2,4-dichlorophenol and 4-chloroaniline as TBPs had a relatively higher toxicity to Vibrio fischeri (a marine bacterial species) than Daphnia magna (a freshwater plankton species).

Tea plant is capable of hyper-accumulating fluoride (F) in leaves, suggesting drinking tea may cause excessive F intake in our body and threaten the health. This study investigated the changes in the structure, composition, and F content in the leaf cell wall of the tea (Camellia sinensis) under different F conditions to demonstrate the role of cell wall in F enrichment in tea plants. The cell wall was shown as the main part for F accumulation (67%–92%), with most of F distributed in the pectin fraction (56%–71%). With increasing F concentration, a significant increase (p < 0.05) was observed in the F content of cell wall and its components, the level of cell wall metal ions (i.e. Cu, Mg, Zn, Al, Ca, Ba, Mn), as well as the content of total cell wall materials, cellulose, and pectin. Meanwhile, the level of Cu, Mg, Zn, pectin, and cellulose was significantly positively correlated with the F content in the leaf cell wall. F addition was shown to increase the fluorescence intensity of LM19 and 2F4 antibody-labeled low-methylesterified homogalacturonans (HGs), while decrease LM20-labeled high-methylesterified HGs, coupled with an increase in the activity and gene expression of pectin methyl esterases (PMEs) in tea leaves. All these results suggest that F addition can increase pectin content and demethylesterification, leading to increased absorption of metal cations and chelation of F in the cell wall through the action of metal ions.

Dioxins are highly injurious environmental pollutants with proven toxicological effects on both animals and humans, but to date their effects on plants still need to be studied in detail. We identified a dioxin-inducible caleosin/peroxygenase isoform, PdPXG4, that is mostly expressed in leaves of date palm seedlings and exhibits a specific reductase activity towards the 13-hydroperoxide of C18:2 and C18:3 (HpODE and HpOTrE, respectively). After exposure to TCDD, lipid droplets (LDs) isolated from TCDD-exposed leaves were about 6.5–15.7-fold more active in metabolizing 13-HpOTrE compared with those isolated from non-exposed leaves. A characteristic spectrum of leaf dioxin-responsive oxylipins (LDROXYL) was detected in dioxin-exposed seedlings. Of particular importance, a group of these oxylipins, referred to as Class I, comprising six congeners of hydroxides fatty acids derived from C18:2 and C18:3, was exclusively found in leaves after exposure to TCDD. The TCDD-induced oxylipin pattern was confirmed in vitro using terbufos, a typical inhibitor towards the PdPXG4 peroxygenase activity. Of particular interest, the response of terbufos-pretreated protoplasts to TCDD was drastically reduced. Together, these findings suggest that PdPXG4 is implicated in the establishment of a dioxin-specific oxylipin signature in date palm leaves soon after their exposure to these pollutants.

Endocrine-disrupting chemicals (EDCs) in diet are a health concern and their monitoring in food has been introduced in the European Union. In developing countries, EDC dietary exposure data are scarce, especially from areas perceived as pollution hotspots, including industrialized countries like India. Several persistent organic pollutants (POPs) act as EDCs and pose a pressure to human health mainly through dietary exposure. In the present study, a range of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), dioxins and furans were measured in several food items collected from Indian urban (Delhi) and peri-urban (Dehradun) areas. Food basket contamination data were used to estimate EDC dietary exposure and compare it with that of the average European population estimated from available monitoring data. All the target contaminants were found in most food items, especially in dairies and meat products. OCPs were the main contributers to the measured EDC contamination. Food supplied to Delhi's markets had higher EDC contamination than that supplied to the peri-urban market in Dehradun. Despite lax compliance and control measures, Indian dietary exposure of OCPs and PBDEs were comparable with that of Europe and were lower for PCBs and dioxins. Higher meat consumption in Europe only partly explained this pattern which was driven also by the higher EDC residues in some European food items. A substantial part of endocrine disrupting potential in the diet derives from food and animal feeds internationally traded between developed and developing countries. With increasingly globalized food systems, internationally harmonized policies on EDC content in food can lead to better protection of health in both these contexts.

We investigated the fates of seven neonicotinoids (NNIs) in full-scale drinking water treatment plants and assessed human exposure to NNIs through consuming drinking water. The total NNI concentrations in raw water and treated water samples from the drinking water treatment plants were 20.4–166 ng/L (median 118 ng/L) and 1.11–94.7 ng/L (median 20.4 ng/L), respectively. The dinotefuran (DIN) concentrations in raw water collected in different seasons were different, and the highest DIN concentration was found in summer. The drinking water treatment processes removed >91% of the NNIs except DIN and thiamethoxam (THIAM), for which the mean removal rates were 70% and 74%, respectively. The removal rates for all of the NNIs were higher for the granular activated carbon filtration process (mean 83.5%) than the other drinking water treatment plant processes (coagulation/sedimentation 22.3%, ozonation 29.2%). However, the removal rates in the granular activated carbon process were lower for DIN and THIAM (61.0% and 59.2%, respectively) than the other NNIs. Significant correlations were found between the NNI removal rates and physicochemical properties (solubility in water and log (octanol–water partition coefficient)). The estimated mean human exposure to NNIs in drinking water was 0.528 ng/(kg body weight d).