The comparison of fly ash generated from lignite combustion in a thermal power plant Kolubara A (Veliki Crljeni) and bottom and fly ash from coal waste combustion in a semi-industrial fluidized bed boiler (Vinča) was performed as the function of particle size. The average total concentrations of the 16 EPA priority PAHs in ash fractions are 0.49 mg kg⁻¹ of ash (thermal power plant) and 17.48 mg kg⁻¹ of ash (fluidized bed boiler). The sum of 3- and 4-ring PAHs accounts for more than 93% of overall PAHs concentration, and the most abundant among them is fluoranthene.The portions of PAHs groups defined based on their physico-chemical properties, as obtained from quantitative structure-activity relationship (QSAR) models included in the Vega platform, were determined. These portions, emission factors, and benzo[a]pyrene equivalence concentrations were further on used to estimate the potential environmental impact of ash disposal. The PAHs emission factors are higher compared to values in the air pollutant emission inventory guidebook of the cooperative program for monitoring and evaluation of the long-range transmission of air pollutants in Europe (EMEP/EEA). The overall emission factors of 16 PAHs for combustion of lignite and coal waste are determined to be 0.15 and 249.97 mg kg⁻¹ of fuel, respectively. Based on the ratios of benzo[a]pyrene equivalence concentrations of each ash and correspondent fuel, the disposal of fly ash from the cyclone of fluidized bed boiler represents the highest risk to the environment among tested ashes.

Effects of mining and metals production have been reported in freshwater lake sediments from around the world but are rarely quantified in saline lake sediments, despite the importance of these lake ecosystems. Here we used dated sediment cores from Great Salt Lake, Utah, USA, a large saline lake adjacent to one of the world’s largest copper mines, to measure historical changes in the deposition of 22 metals. Metal concentrations were low prior to the onset of mining in the catchment in 1860 CE. Concentrations of copper, lead, zinc, cadmium, mercury, and other metals began increasing in the late 1800s, with peaks in the 1950s, concomitant with enhanced mining and smelting activities. Sedimentary metal concentrations in the 1950s were 20-40-fold above background levels for copper, lead, silver, and molybdenum. Concentrations of most metals in surficial sediments have decreased 2-5-fold, reflecting: 1) storage and mineralization of sedimenting materials in a deep brine layer, thereby reducing metal transport to the sediments; 2) improved pollution control technologies, and; 3) reduction in mining activity beginning in the 1970s and 1980s. Despite reductions, concentrations of many metals in surficial sediments remain above acceptable contamination thresholds for aquatic ecosystems with migratory birds, and consumption advisories for mercury have been placed on three waterfowl species. The research also highlights that metal deposition in saline lakes is complicated by effects of hypersaline brines and deep-water anoxia in regulating sediment redox and release of metals to surface waters. Given the importance of saline lakes to migratory birds, metals contamination from mining and metals production should be a focus of saline lake remediation.

Naphthalene sulfonic acids (NSAs) are used extensively in industrial applications as dispersants in dyes, rubbers, and pesticides, and as anti-corrosive agents in coatings, gels, and sealants. This study examined the toxicity of three NSA congeners, barium dinonylnaphthalene sulfonate (BaDNS), calcium dinonylnaphthalene sulfonate (CaDNS), and dinonylnaphthalene disulfonic acid (DNDS), to two benthic species, Tubifex tubifex and Hyalella azteca. Two substrates with different levels of organic carbon (sediment [2%] and sand [0%]) were used in toxicity tests. Juvenile production was the most sensitive endpoint for T. tubifex: the 28-d EC50s were <18.2, 22.2, and 64.0 μg/g dw in sand and 281.3, 361.6, and 218.9 μg/g dw in sediment for BaDNS, CaDNS, and DNDS, respectively. The 28-d LC50s for H. azteca were similar among compounds: 115.3, 82.1, and 49.0 μg/g dry weight (dw) in sand, and 627.3, 757.9, and >188.5 μg/g dw in sediment, for BaDNS, CaDNS, and DNDS, respectively. However, when LC50s were estimated based on concentrations of NSAs measured in overlying water (which can be an important route of exposure for H. azteca), BaDNS and CaDNS were 3–4 orders of magnitude more toxic than DNDS. The NSAs examined were >3-fold more toxic when present in substrates with no organic carbon (e.g., sand) for all H. azteca endpoints where LC/EC50s could be calculated and for sublethal endpoints for T. tubifex. The organic carbon content of the sediment appears to have acted as a sink and reduced NSA toxicity by decreasing bioavailability. Environmental sediment samples were collected from 12 river sites across southern Ontario. The maximum concentration of CaDNS observed in sediment collected from this region was 2.8 μg/g dw in sediment with 2% organic carbon; 100-fold lower than the lowest EC10 in the current study.

This study aimed to evaluate the impacts of morphological-controlled ZnO nanoarchitectures on aerobic microbial communities during real wastewater treatment in an aerobic-photocatalytic system. Results showed that the antibacterial properties of ZnO nanoarchitectures were significantly more overwhelming than their photocatalytic properties. The inhibition of microbial activities in activated sludge by ZnO nanoarchitectures entailed an adverse effect on wastewater treatment efficiency. Subsequently, the 16S sequencing analysis were conducted to examine the impacts of ZnO nanoarchitectures on aerobic microbial communities, and found the significantly lower microbial diversity and species richness in activated sludge treated with 1D-ZnO nanorods as compared to other ZnO nanoarchitectures. Additionally, 1D-ZnO nanorods reduced the highest proportion of Proteobacteria phylum in activated sludge due to its higher proportion of active polar surfaces that facilitates Zn²⁺ ions dissolution. Pearson correlation coefficients showed that the experimental data obtained from COD removal efficiency and bacterial log reduction were statistically significant (p-value < 0.05), and presented a positive correlation with the concentration of Zn²⁺ ions. Finally, a non-parametric analysis of Friedman test and post-hoc analysis confirmed that the concentration of Zn²⁺ ions being released from ZnO nanoarchitectures is the main contributing factor for both the reduction in COD removal efficiency and bacterial log reduction.

The transmission and accumulation of trace metals in marine food webs have a profound influence on the structure and function of marine environment. In order to quantitatively assess the trophic transfer behaviors of eight common metals (As, Cd, Cr, Cu, Hg, Ni, Pb and Zn) in simplified five-trophic level marine food webs, a total of 9929 biological samples from 61 studies published between 2000 and 2019, involving 154 sampling sites of 33 countries/regions, were re-compiled using meta-analysis. Based on concentration-trophic level weighted linear regression and predator/prey comparison, the food web magnification factor (FWMF) and the biomagnification factor (BMF) were calculated, respectively. The results showed dissimilar trophic transfer behaviors of these metals in global marine food webs, in which As and Ni tended to be efficiently biodiluted with increasing trophic levels (FWMFs < 1, p < 0.01), while Hg, Pb and Zn trophically biomagnified (FWMFs > 1, p < 0.05). However, Cd, Cr and Cu presented no biomagnification or biodilution trend (p > 0.05). The values of FWMFs were ranked as: Hg (2.01) > Pb (1.81) > Zn (1.15) > Cu (1.13) > Cr (0.951) > Cd (0.850) > Ni (0.731) > As (0.494). In terms of specific predator-prey relationship, Pb showed significant biodilution from tertiary consumers (TC) to top predators (BMF < 1, p < 0.05), whereas Cd and Cu displayed obvious biomagnification from primary consumers (PC) to secondary consumers (SC) (BMFs >1, p < 0.05). Additionally, when Cu and Zn were transferred from SC to TC, and primary producers to PC, clear biodilution and biomagnification effects were observed, respectively (p < 0.05). Further analysis indicated that the average concentration of Hg in five-trophic level marine food webs of developed countries (0.904 mg kg⁻¹ dw) was more noticeable (p < 0.05) than that of developing countries (0.549 mg kg⁻¹ dw).

The application of roadway deicing salts is increasing the salinity of freshwater systems. Increased salinization from salts, such as NaCl, CaCl₂ and MgCl₂, can have direct, negative impacts on freshwater organisms at concentrations found in nature. Yet, our understanding of how these salts can indirectly impact freshwater organisms by altering important ecological interactions, such as those between hosts and their parasites, is limited. Using a larval amphibian and infectious free-living helminth (i.e. trematode) model, we examined whether exposure to environmentally relevant concentrations of NaCl, CaCl₂ and MgCl₂ 1) influence trematode mortality; 2) alter amphibian-trematode interactions; and 3) alter larval amphibian activity (a behavior associated with parasite avoidance). We found that exposure to CaCl₂ greatly reduced trematode survival across all Cl⁻ concentrations (230, 500, 860 and 1000 mg Cl⁻ L⁻¹) while NaCl and MgCl₂ had no effect. When both host and parasites were exposed to the salts, exposure to NaCl, but not MgCl₂ or CaCl₂, increased infection. The lack of effect of CaCl₂ on infection was likely driven by CaCl₂ reducing trematode survival. Exposure to NaCl increased infection at 500 mg Cl⁻ L⁻¹, but not 230 or 860 mg Cl⁻ L⁻¹. Increased infection was not due to salt exposure altering tadpole behavior. Our results suggest that NaCl can negatively impact amphibian populations indirectly by increasing trematode infections in tadpole hosts.

Microplastics have received growing attention as carriers of organic pollutants in the water environment. To better understand the contribution of hydrophobic interaction, hydrogen-bonding interaction, π-π interaction and electrostatic interaction on the adsorption of hydrophilic compounds on microplastics and their adsorption behavior in natural waters, polyethylene terephthalate (PET, <150 μm) was used as an adsorbent and 4-chlorophenol (MCP), 2,4-dichlorophenol (DCP) and 2,4,6-trichlorophenol (TCP) were used as adsorbates. The results of batch adsorption experiments showed that chlorophenols (CPs) reached adsorption sites of PET through film diffusion and intra-particle diffusion. pH greatly affected the adsorption capacity. Hydrophobic interaction was the main adsorption mechanism of undissociated CPs on PET. Hydrogen-bonding interaction was also an adsorption mechanism between undissociated CPs and PET, and the contribution of hydrogen-bonding interaction to adsorption decreased with the increase of chlorine content. Meanwhile, the increase of chlorine content was favorable to the hydrophobic interaction between undissociated CPs and PET. However, higher chlorine content CPs with lower pKₐ values tended to dissociate at neutral pH condition and resulted in stronger electrostatic repulsion with PET. The increase of solution ionic strength and fulvic acid content negatively affected the adsorption of DCP and TCP on PET, but did not show significant impacts on MCP adsorption. Similarly, the adsorption capacity obtained using Taihu lake water and Bohai seawater as matrices was much lower than that using laboratory water for both DCP and TCP, while the adsorption coefficient (Kd) of MCP remained at approximately 10.6 L/kg to 11.4 L/kg in the three different solution matrices. The Kd values exhibited using natural water matrices consistently followed the order of DCP > MCP > TCP. This study provides insights into the fate of CPs in the presence of microplastics and suggests that the potential risks posed by CPs and microplastics to aqueous ecosystems merit further investigation.

Microplastics have attracted much attention in recent years as they can interact with pollutants in water environment. However, nanoplastics (NPs) with or without the surface functionalization modification have not been thoroughly explored. Here, the sorption behaviors of two fluoroquinolones (FQs), including norfloxacin (NOR) and levofloxacin (LEV) on polystyrene NPs (nano-PS) and carboxyl-functionalized polystyrene NPs (nano-PS-COOH) were investigated. The results showed that sorption isotherms were nonlinear and well fitted by Langmuir model. The sorption capacities of NOR and LEV on nano-PS-COOH were higher than those on nano-PS, and their physical interactions, including polar interaction, electrostatic interaction and hydrogen bonding may be the dominant mechanisms. Moreover, the increase of pH firstly increased the sorption of two FQs on NPs and then decreased because NOR and LEV had a reverse charge at different pH values. Salinity and dissolved organic matter both inhibited the sorption process. These findings show that NPs with or without the surface functionalization modification have different sorption behaviors for environmental pollutants, which deserve our further concern.

Decades of large-scale production of per- and polyfluoroalkyl substances (PFASs) have resulted in their ubiquitous presence in the environment worldwide. Similarly to other persistent and bioaccumulative organic contaminants, some PFASs, particularly the long-chain congeners, can be biomagnified via food webs, making top predators vulnerable to elevated PFAS exposure. In this study, we measured seven classes of PFASs in bald eagle (Haliaeetus leucocephalus) eggs for the first time. The eggs (n = 22) were collected from the North American Great Lakes in 2000–2012. The ranges of total concentrations of perfluoroalkyl sulfonic acids (∑PFSAs) and perfluoroalkyl carboxylic acids (∑PFCAs) were 30.5–1650 and 5.4–216 ng/g wet weight (ww), respectively. In addition to these traditional PFAS compounds, 6:2 fluorotelomer sulfonic acid (6:2 FTS; median: 15.7 ng/g ww), perfluoro-4-ethylcyclohexanesulfonic acid (PFECHS; 0.22 ng/g ww), and 8-chloro-perfluorooctanesulfonic acid (Cl-PFOS, detected in wildlife for the first time; 0.53 ng/g ww) were also frequently detected. Bald eagle eggs from breeding areas located less than 8 km from a Great Lake shoreline or tributary had significantly greater total PFAS concentrations (∑PFASs) than those from breeding areas located further than 8 km (p < 0.05). In these samples, ∑PFASs rivalled the total concentration of brominated flame retardants, and were significantly greater than those of several other organic contaminants, such as dechlorane-related compounds, organophosphate esters, and flame retardant metabolites.

Microplastics have been increasingly documented in freshwater ecosystems in recent years, and growing concerns have been raised about their potential environmental health risks. To assess the current state of knowledge, with a focus on the UK, a literature review of existing freshwater microplastics studies was conducted. Sampling and analytical methodologies currently used to detect, characterise and quantify microplastics were assessed and microplastic types, sources, occurrence, transport and fate, and microplastic-biota interactions in the UK’s freshwater environments were examined. Just 32% of published microplastics studies in the UK have focused on freshwater environments. These papers cover microplastic contamination of sediments, water and biota via a range of methods, rendering comparisons difficult. However, secondary microplastics are the most common type, and there are point (e.g. effluent) and diffuse (non-point, e.g. sludge) sources. Microplastic transport over a range of spatial scales and with different residence times will be influenced by particle characteristics, external forces (e.g. flow regimes), physical site characteristics (e.g. bottom topography), the degree of biofouling, and anthropogenic activity (e.g. dam release), however, there is a lack of data on this. It is predicted that impacts on biota will mirror that of the marine environment. There are many important gaps in current knowledge; field data on the transport of microplastics from diffuse sources are less available, especially in England. We provide recommendations for future research to further our understanding of microplastics in the environment and their impacts on freshwater biota in the UK.