Our world is awash with plastic. The massive increase in plastics production, combined with a shift to single-use, disposable plastics and widespread mismanagement of plastic waste, has created a huge “tragedy of the commons” (Hardin, 1968) in our oceans, seas and waterways. Plastics pollution is now a global externality that damages ecosystems, curtails biodiversity and ultimately has the potential to affect everyone on the planet. Although waste output is often modelled separately from environmental pollution in research, in the case of plastics, the waste problem has become one of global pollution. In this paper, we model the relationship between mismanaged plastic waste1 and income per capita for 151 countries, and for the first time find empirical support for the environmental Kuznets curve using plastics pollution data. Further, we find support for the hypothesis that a key instrument for reducing plastics pollution is investment in scientific and technological research. The paper concludes with a discussion of the results, limitations, and implications for future research and practice.

The heavy metal ion adsorption performance of birnessite (a layer-structured manganese oxide) can be enhanced by decreasing the Mn average oxidation state (Mn AOS) and dissolution−recrystallization during electrochemical redox reactions. However, the electrochemical adsorption processes of heavy metal ions by tunnel-structured manganese oxides are still enigmatic. Here, tunnel-structured manganese oxides including pyrolusite (2.3 Å × 2.3 Å tunnel), cryptomelane (4.6 Å × 4.6 Å tunnel) and todorokite (6.9 Å × 6.9 Å tunnel) were synthesized, and their electrochemical adsorptions for Cd²⁺ were performed through galvanostatic charge−discharge. The influence of both supporting ion species in the tunnel and tunnel size on the electrochemical adsorption performance was also studied. The adsorption capacity of tunnel-structured manganese oxides for Cd²⁺ was remarkably enhanced by electrochemical redox reactions. Relative to K⁺ in the tunnel of cryptomelane, the supporting ion H⁺ was more favorable to the electrochemical adsorption of Cd²⁺. With increasing initial pH and specific surface area, the electrochemical adsorption capacity of cryptomelane increased. The cryptomelane electrode could be regenerated by galvanostatic charge−discharge in Na₂SO₄ solution. Due to the differences in their tunnel size and supporting ion species, the tunnel-structured manganese oxides follow the order of cryptomelane (192.0 mg g⁻¹) > todorokite (44.8 mg g⁻¹) > pyrolusite (13.5 mg g⁻¹) in their electrochemical adsorption capacities for Cd²⁺.

Malaysia depends heavily on rivers as a source for water supply, irrigation, and sustaining the livelihood of local communities. The evolution of land use in urban areas due to rapid development and the continuous problem of illegal discharge have had a serious adverse impact on the health of the country's waterways. Klang River requires extensive rehabilitation and remediation before its water could be utilised for a variety of purposes. A reliable and rigorous remediation work plan is needed to identify the sources and locations of streams that are constantly polluted. This study attempts to investigate the feasibility of utilising a temporal and spatial risk quotient (RQ) based analysis to make an accurate assessment of the current condition of the tributaries in the Klang River catchment area. The study relies on existing data sets on Biochemical Oxygen Demand (BOD), Chemical Oxygen Demand (COD), Total Suspended Solids (TSS), and Ammonia (NH₃) to evaluate the water quality at thirty strategic locations. Analysis of ammonia pollution is not only based on the limit established for river health but was expanded to include the feasibility of using the water for water intake, recreational activities, and sustaining fish population. The temporal health of Klang River was evaluated using the Risk Matrix Approach (RMA) based on the frequency of RQ > 1 and associated colour-coded hazard impacts. By using the developed RMA, the hazard level for each parameter at each location was assessed and individually mapped using Geographic Information System (GIS). The developed risk hazard mapping has high potential as one of the essential tools in making decisions for a cost-effective river restoration and rehabilitation.

There is a growing interest in the occurrence and sources of pharmaceutical substances in the environment. This paper reports the first detailed transect of pharmaceutical occurrence along the River Thames, UK, from source to sea, undertaken during a period of high flow in 2016. In 37 samples a total of 41 pharmaceuticals and 2 lifestyle compounds (cocaine and sucralose) were detected. Total concentration of pharmaceuticals ranged from 0.0012 μg/l to 10.24 μg/l with a median of 2.6 μg/l. Sucralose concentrations varied from <0.01 to 5.9 μg/l with a median concentration of 1.93 μg/l and was detected in every sample except the groundwater-dominated sources of the Thames. Antimicrobials, including those on the surface water watch list (erythromycin, clarithromycin and azithromycin) were detected in every site downstream of the Thames source. Diclofenac, recently on the surface water watch list, was detected in 97% of Thames samples and above the proposed EQS of 0.1 μg/l in 12 samples. Distinct increases in concentration and number of pharmaceuticals were found downstream of the Oxford, Mogdon and Hogsmill wastewater treatment works (WWTW) but were more subdued downstream of the Crossness and Beckton WWTW due to the tidal nature of the Thames and combined sewer outflows. Sucralose was found to be an excellent tracer of wastewaters (treated and untreated) and can be used as a proxy for many pharmaceuticals. Paracetamol and ibuprofen were tracers of untreated wastewater inputs to the Thames due to their high biodegradation within WWTWs.

The government of China has announced an ambitious plan to expand the mandatory use of ethanol blended gasoline fuels by 2020. Given the dissimilarity in fuel properties between China and other countries with ethanol blending practices, it is necessary to assess the energy and environmental impacts of ethanol blending. In this study, we prepared two types of ethanol blended fuels (E10, with ethanol contents of approximately 10%) with lower contents of aromatics (ELA) and olefins (ELO), respectively, compared with the market China 5 gasoline. Nine in-use gasoline vehicles varying by manufacturer, engine technology, model year, and emission standard level were analyzed using a chassis dynamometer, which followed the Worldwide Harmonized Light Vehicles Test Cycle (WLTC). Two major positive effects from using E10 fuels could be observed in this study. First, tested turbocharged gasoline direct injection (GDI) vehicles could gain reductions in CO₂ emission, fuel consumption and energy consumption by switching to the higher-octane-number ELO. This finding, along with the engine development trends in the automotive industry (e.g., downsizing and higher compression ratio), may have a synergistic effect to deliver greater energy efficiency in the future. Second, the two ethanol blended fuels could be more effective in reducing the particle mass (PM) and particle number (PN) emissions than the levels of using China 5 gasoline. Notably, the benefit of using ELO was more significant, with average emission reductions of 35% for the PM and of 44% for the PN. However, ELA and ELO possibly increased emissions of gaseous pollutants for certain vehicles in the study, but the intra-vehicle differences between the various fuel groups were not statistically significant (not significant, p > 0.05, t-test). We suggest that more measurements under various environmental conditions and comprehensive air quality simulations should be conducted to better understand the environmental impacts of ethanol blending in China.

Mobile genetic elements (MGEs) play critical roles in transferring antibiotic resistance genes (ARGs) among different microorganisms in the environment. This study aimed to explore the fate of MGEs during chicken manure (CM) and bovine manure (BM) composting to assess horizontal transfer risks of ARGs. The results showed that the removal efficiency of MGEs during CM composting was significantly higher than that during BM composting, because the potential host bacteria of MGEs were eliminated largely during CM composting. Meanwhile, these potential host bacterial communities are significantly influenced by pH, NH4+, NO3− and total N, which can be used to regulate host bacterial communities to remove MGEs during composting. Projection pursuit regression further confirmed that composting can effectively reduce the horizontal transfer risk of ARGs, especially for CM composting. These results identified the critical roles of host bacterial communities in MGEs removal during composting of different animal manures.

Thousands of chemicals exist in hydraulic-fracturing (HF) fluids and wastewater from unconventional oil gas development. The carcinogenicity of these chemicals in HF fluids and wastewater has never been systematically evaluated.In this study, we assessed the carcinogenicity of 1,173 HF-related chemicals in the HF chemical data from the US Environmental Protection Agency (EPA).We linked the HF chemical data with the agent classification data from the International Agency for Research on Cancer (IARC) at the World Health Organization (WHO) (N = 998 chemicals) to evaluate human carcinogenic risk of the chemicals and with the Carcinogenic Potency Database (CPDB) from Toxnet (N = 1,534 chemicals) to evaluate potential carcinogenicity of the chemicals.The Chemical Abstract Service Registry Numbers (CASRNs) for chemicals were used for data linkage. Among 1,173 chemicals, 1,039 were identified only in HF fluids, 97 only in wastewater, and 37 in both. Compared with IARC, we found information of 104 chemicals, and 48 of them may have potentially carcinogenic risk to human, among which 14 are definitely carcinogenic, 7 probably carcinogenic, and 27 possibly carcinogenic. Using the CPDB data, it suggests that 66 chemicals are potentially carcinogenic based on rats and mouse models.Conclusions Our evaluation suggests that exposure to some chemicals in HF fluids and wastewater may increase cancer risk, and the identified chemicals could be selected as the priority list for drinking water exposure assessment or cancer-related health studies.

This study investigated the potential of biochar filters as a replacement for, or complement to, sand filters for removal of per- and polyfluoroalkyl substances (PFASs) from wastewater in on-site wastewater treatment systems (OWTSs). Concentrations and removal of nine perfluoroalkyl carboxylates (PFCAs; C₃₋₁₁) and three perfluoroalkane sulfonates (PFSAs; C₄, ₆, ₈) and one perfluorooctanesulfonamide (FOSA; C₈) were investigated over 22 weeks in four treatments with column filters: biochar (BC) without biofilm (BC-no-biofilm), biochar with active biofilm (BC-active-biofilm), biochar with inactive biofilm (BC-inactive-biofilm) and sand with active biofilm (Sand-active-biofilm). The filters were operated under hydraulic loading (50 L m⁻² day⁻¹) to mimic the loading rate in on-site filtration beds. The initial concentrations of the ΣPFASs in the influent were in the range of 1500–4900 ng L⁻¹. In BC-no-biofilm, the removal efficiency (20–60%) and adsorption capacity (0–88 ng ΣPFASs g⁻¹ BC) of short-chain PFCAs (C₃₋₆) and PFSA (C₄) was low, whereas the removal efficiency (90–99%) and the adsorption capacity (73–168 ng g⁻¹) was high for C₇-C₁₁ PFCAs, C₆, C₈ PFSAs and FOSA. The relative removal was generally lower for C₃₋₉ PFCAs and C₄, C₆, C₈ PFSAs using BC-active-biofilm and BC-inactive-biofilm compared with BC-no-biofilm. This can be explained by the presence of biofilm and solids in BC-active-biofilm and the presence of wastewater solids in BC-inactive-biofilm, which decreased the availability and number of adsorption sites for PFASs compared with BC-no-biofilm. On the other hand, inactivation of the biofilm resulted in lower removal efficiencies for C₅₋₁₁ PFCAs, C₄, C₆, C₈ PFSAs and FOSA, probably because the biofilm degraded organic matter and thus increased the availability and number of adsorption sites compared with BC-inactive-biofilm. Sand-active-biofilm showed poor removal (0–70%) for all PFASs except FOSA (90%) and its adsorption capacity was low (0.0–7.5 ng g⁻¹). In general, for all biochar treatments, shorter-chain PFASs were more resistant to removal than longer-chain PFASs. In addition, C₄, C₆ and C₈ PFSAs showed 10–30%, 10–50% and 20–30% higher average removal efficiency, respectively, than PFCAs with corresponding perfluoroalkyl chain length. In conclusion, biochar is a promising filter medium for removal of PFASs in OWTSs, especially for PFASs with a perfluorocarbon chain longer than C₆.

As a developed city in North China, Tsingtao is believed to be suffering from the pollution of polybrominated diphenyl ethers (PBDEs) due to the rapid industrialization and urbanization in recent years. In this work, 8 PBDE congeners were detected in sediments from Moshui River, Tsingtao. BDE-209 and sum of 7 low brominated PBDE congeners (∑₇PBDEs, excluding BDE-209) ranged from 10.2 × 10⁻³ to 237 × 10⁻³ mg kg⁻¹ and from 1.62 × 10⁻³ to 23.1 × 10⁻³ mg kg⁻¹ d.w., respectively. PBDE concentrations decreased in the order of midstream > downstream > upstream, attributing to the discrepancies in anthropogenic activities among these areas. Principal component analysis coupled with multiple linear regression (PCA-MLR) revealed that 24.4% of PBDEs were derived from surface runoff of contaminated soils, 58.2% from direct discharge of local sources and 17.4% from atmospheric deposition. The probabilistic health risk assessment of PBDEs was performed by using Monte Carlo simulation. The carcinogenic and non-carcinogenic risks based on total PBDEs were low for children and teens, whilst severe for adults. However, based on bioaccessible PBDEs (in vitro gastrointestinal model), there was no obvious health risk for the three age groups. To the best of our knowledge, the present study was the first attempt to assess the health risk by using bioaccessible PBDEs in sediments.

Cigarette smoke is an important indoor air pollutant which has deleterious effects on human health. Continued daily exposure to cigarette smoke has been attributed to the risk factor of ocular surface diseases. However, the mechanisms underlying the ocular surface damage are not fully elucidated. In this study, exposure to cigarette smoke extract (CSE) induced a dose- and time-dependent cytotoxicity in human corneal epithelial (HCE) cells, supported by the observation of reduced cell viability, increased apoptotic cells, elevated intracellular oxidative stress and loss of mitochondrial transmembrane potential. In addition, CSE exposure led to the impairment of proteostasis and autophagy, which resulted in the accumulation of ubiquitinated proteins as aggregates in peri-nuclear spaces. Furthermore, the autophagy inducer, cysteamine was shown to attenuate the CSE induced cell damage, oxidative stress and mitochondrial dysfunction in HCE cells. Moreover, cysteamine inhibited the formation of ubiquitin-positive aggregates around the peri-nuclear region, through regulating the autophagic activity of HCE cells. Similar to in vitro experiments, cigarette smoke induced proteostasis and autophagy impairment in corneal epithelial cells could be rescued by cysteamine in a cigarette smoke-exposed murine model. Therefore, this study may provide first evidence that dysfunction of autophagy contributes to the pathogenesis of ocular surface diseases associated with cigarette smoke exposure. Besides, it also suggests the potential therapeutic value of cysteamine in the prevention and treatment of cigarette smoke induced ocular surface injury.CSE induces cytotoxicity and accumulation of ubiquitinated proteins in HCE cells due to impairment of proteostasis and autophagy, which can be rescued by cysteamine.