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.

Oil-contaminated soils resulted from drilling activities can cause significant damages to the environment, especially for living organisms. Treatment and management of these soils are the necessity for environmental protection. The present study investigates the field study of seven oil-contaminated soils treated by different stabilization/solidification (S/S) methods, and the selection of the best treated site and treatment method. In this study, first, the ratios of consumed binders to the contaminated soils (w/w) and the treatment times for each unit of treated soils were evaluated. The ratios of consumed binders to the contaminated soils were between 6 and 10% and the treatment times for each unit of treated soils were between 4.1 and 18.5 min/m³. Physicochemical characteristics of treated soils were also determined. Although S/S methods didn’t change the water content of treated soils, they increased the porosity of soils. Unexpectedly, the cement-based S/S methods didn’t increase the pH of the treated soils. The highest and the lowest leaching of petroleum hydrocarbons was belonging to S/S using diatomaceous earth (DE) and the combination of Portland cement, sodium silicate and DE (CS-DE), respectively. The best acid neutralization capacity was obtained for soils treated using the combination of Portland cement and sodium silicate (CS). Based on the best-worst multi-criteria decision-making method (BWM-MCDM), the soils treated using CS-DE was select as the best. The BWM-MCDM can be used as an effective tool for the selection of the best alternative in all areas of environmental decontamination.

Decabromodiphenyl ether (DecaBDE) is a brominated flame retardant belonging to the group of polybrominated diphenyl ethers. DecaBDE has been widely used for various applications, such as plastics, textiles, and building and construction materials. Limited information on DecaBDE production and usage inventory has been elaborated, however. Therefore, this work aimed to produce a preliminary emissions inventory of DecaBDE in mainland China by estimating production and consumption amounts of DecaBDE, and characterizing its emission factors during production and usage, based on industrial investigation and theoretical prediction. It was indicated that the total production of DecaBDE reached 464.68 thousand metric tons (kt), of which 62.72 kt were exported, since the beginning of its production. Shandong and Jiangsu provinces dominate the production, with proportions of 77.95% and 18.45%, respectively. The production stage releases most of the DecaBDE to the atmosphere, with an emissions factor of 23 ± 1.9 kg/t, followed by 20 ± 0.9 kg/t DecaBDE to waste water and 16 ± 1.0 kg/t DecaBDE as solid residue. DecaBDE emissions in the consumption stage—namely the plastic production process—are 0.17 ± 0.06–0.23 ± 0.08 kg DecaBDE to the atmosphere and 1.72 ± 0.58–2.29 ± 0.77 kg DecaBDE to solid residue, for each metric ton of plastic produced. The total annual DecaBDE emissions to waste water are 93.98–1140.9 mg—negligible. The results showed that the sources of DecaBDE environmental pollution are its manufacturing and flame-retardant plastic modification plants, which are easily overlooked by both the government and the public. Yet DecaBDE emissions elimination and the environmentally sound management of the DecaBDE waste generated from these two processes are crucial for environmental protection.

In this study, levels of dechlorane plus (DP) in breast milk and matched adipose tissue samples were measured from 54 women living in Wenling, China. Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were measured simultaneously for comparison. The levels of ∑DPs/∑PBDEs varied from less than one to several dozens of ng g⁻¹ lipid weight (lw) in matrices and the levels of ∑PCBs varied between several to hundreds of ng g⁻¹ lw. In the same matrix, ∑DPs and ∑PCBs/∑PBDEs showed a significant relationship (p < 0.05), indicating that they shared common sources. Accordingly, there was a strong association of lipid-adjusted concentrations of individual compounds (BDE-209 excluded) between matrices (p < 0.001), suggesting that breast milk could be a proxy for adipose tissue in human bioburden monitoring of these compounds. The predicted lipid-adjusted milk/adipose ratios varied from 0.62 to 1.5 but showed significant differences (p<0.001) between compounds, suggesting a compound-specific transfer between milk lipids and adipose tissue lipids. Specifically, the milk/adipose ratios for syn-DP and anti-DP (−1.40 and 1.3, respectively) were significantly higher than those of CB congeners and hexa/hepta-BDE congeners (p < 0.05). In addition, unlike PCBs/PBDEs (excluding BDE-209), DP’s hydrophobicity might not be responsible for its preferable distribution in milk lipids. Instead, the interaction with nonlipid factors played a key role. The fraction of anti-DP between the two kinds of matrices was not significantly different, suggesting that the biochemical transfer processes may not be efficient enough to distinguish DP isomers. Nevertheless, the congener patterns of PCBs/PBDEs gave a clue about the compound-specific transfer between milk and adipose tissue. To our knowledge, this is the first to report the relationships of DP between adipose tissue and breast milk. These results could provide useful and in-depth information on biomonitoring of DP and facilitate the understanding of the accumulation and excretion potentials of DP and its distribution-related mechanism in humans.

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.

Cadmium (Cd) as a highly toxic heavy metal can cause seriously harmful to human health. Rice consumption is a major source of Cd intake by Chinese. Reduce the Cd accumulation by rice is the key for reducing Cd hazard. Therefore, fly ash (FA) was used as raw material in this study, after the process of simplifying hydrothermal synthesis the zeolite (ZE), which was named as low-temperature-alkali roasting, a new intermediate materials (IP) was got. And the three mentioned materials (FA, IP and ZE) were used for a two-year field experiment. The study demonstrated that, application of IP and ZE could promote rice growth, as well as increase soil pH, and improve available Si content. The rice production increased by 36.1% and 29.8% in 2017 by IP and ZE applied, enhanced 35.9% and 31.7% in 2018, respectively. Meanwhile, the bio-available Cd decreased by 26.9% and 26% in 2017, reduced by 22.9% and 28% in 2018, respectively. Generally, the passivators could promote the conversion of acid-exchangeable fraction Cd to reducible fraction Cd. It can be conclude that, IP and ZE have good remediation effect on contaminated soil, and alleviated effects on Cd accumulation by rice, even though no significant difference was detected between IP and ZE. The synthesis process of IP of is simpler than ZE. The impact of IP on contaminated soil needs further exploration.

3-Acetyldeoxynivalenol (3-Ac-DON), the acetylated derivative of deoxynivalenol (DON), has been reported to be coexisted with DON in various cereal grains. Ingestion of grain-based food products contaminated by 3-Ac-DON might exert deleterious effects on the health of both humans and animals. However, the biological toxicity of 3-Ac-DON on macrophages and the underlying mechanisms remain largely unknown. In the present study, we showed that RAW 264.7 macrophages treated with 0.75 or 1.50 μg/mL of 3-Ac-DON resulted in DNA damage and the related cell cycle arrest at G1 phase and cell death, activation of the ribotoxic stress and the endoplasmic reticulum (ER) stress responses. The 3-Ac-DON-induced cell death was accompanied by a protective autophagy, because gene silencing of Atg5 using the small interfering RNA enhanced cell death. Results of further experiments revealed a role for lysosomal membrane permeabilization in the 3-Ac-DON triggered inhibition of autophagic flux. Additional work also showed that increased lysosomal biogenesis and leakage of cathepsin B (CTSB) from lysosomes to cytosol was critical for the 3-Ac-DON-induced cell death. Importantly, 3-Ac-DON-induced DNA damage and cell death were rescued by CA-074-me, a CTSB inhibitor. Collectively, these results indicated a critical role of lysosomal membrane permeabilization in the 3-Ac-DON-induced apoptosis of RAW 264.7 macrophages.

Metals sequestered in coastal sediments are normally considered to be stable, but this investigation shows – somewhat surprisingly – that mercury concentrations in a previously contaminated area, Harboøre Tange, Denmark, have decreased since the 1980s. Mercury concentrations were determined in sediment and benthic biota and present values were compared to values in the 1980s and values from areas without known; history of mercury contamination. Concentrations in both the upper 20 cm of the sediments and; biota are considerably lower now compared to latest monitoring (1980s). Sediment.concentrations at most locations have decreased from the 100–300 ng Hg g⁻¹ dry weight (dw) level to levels below the Background Concentration (BC) of 50 ng Hg g⁻¹ dw defined by Oslo-Paris Convention for the Protection of the Marine Environment of the North-East Atlantic; some stations are at the 2–10 ng Hg g⁻¹ dw level characteristic of Danish coastal sediments with no known history of mercury contamination. Concentrations of mercury in the benthic biota along Harboøre Tange have also decreased since the 1980s but despite the lowered mercury concentrations in the sediments, concentrations in most samples of benthic invertebrate fauna still exceed those in uncontaminated coastal areas and also the Environmental Quality Standard (EQS) of 20 ng Hg g⁻¹ wet weight (≈100 ng Hg g⁻¹ dry weight) defined by the European Union’s Water Framework Directive. Concentration ranges in selected organisms are: (Harboøre Tange l980s/Harboøre Tange now/uncontaminated areas - given in ng Hg g⁻¹ dw): Periwinkles Littorina littorea 9000/150–450/55-77, blue mussels Mytilus edulis up to 9000/300–500/40–170, cockles Cerastoderma edule up to 8000/400–1200/200, brown shrimp Crangon crangon 700–2200/150-450/47, eelgrass Zostera marina up to 330/25–70/12. The present results - together with a literature review - show that a simple and straight forward relationship between the concentrations of mercury in sediment and benthic organisms does not necessarily exist.

In this study, the seasonal characteristics of microbial community compositions at different sites in a river under anthropogenic disturbances (Maozhou River) were analyzed using Illumina HiSeq sequencing. Taxonomic analysis revealed that Proteobacteria was the most abundant phylum in all sites, followed by Actinobacteria, Bacteroidetes, Chloroflexi, Acidobacteria and Firmicutes. The variations of the community diversities and compositions between the seasons were not significant. However, significant differences between sites as well as water and sediment samples were observed. These results indicated that sites under different levels of anthropogenic disturbances have selected distinct bacterial communities. pH, dissolved oxygen (DO), concentrations of total nitrogen (TN) and heavy metals were the main factors that influence the diversity and the composition of bacterial community. Specifically, the relative abundance of Proteobacteria was negatively correlated with pH and DO and positively correlated with TN, while Actinobacteria and Verrucomicrobia showed the opposite pattern. Moreover, positive correlations between the relative abundances of Firmicutes and Bacteroidetes and the concentration of heavy metals were also found. Results of functional prediction analysis showed no significant differences of the carbon, nitrogen and phosphorus metabolism across the sites and seasons. Potential pathogens such as Vibrio, Arcobacter, Acinetobacter and Pseudomonas were found in these samples, which may pose potential risks for environment and human health. This study reveals the effect of anthropogenic activities on the riverine bacterial community compositions and provides new insights into the relationships between the environmental factors and the bacterial community distributions in a freshwater ecosystem under anthropogenic disturbances.

This study aimed to investigate the relationship between outdoor, indoor, and personal PM₂.₅ exposure in the retired adults and explore the effects of potential determinants in two Chinese megacities. A longitudinal panel study was conducted in Nanjing (NJ) and Beijing (BJ), China, and thirty-three retired non-smoking adults aged 43–86 years were recruited in each city. Repeated measurements of outdoor-indoor-personal PM₂.₅ concentrations were measured for five consecutive 24-h periods during both heating and non-heating seasons using real-time and gravimetric methods. Time-activity and household characteristics were recorded. Mixed-effects models were applied to analyze the determinants of personal PM₂.₅ exposure. In total, 558 complete sets of collocated 24-h outdoor-indoor-personal PM₂.₅ concentrations were collected. The median 24-h personal PM₂.₅ exposure concentrations ranged from 43 to 79 μg/m³ across cities and seasons, which were significantly greater than their corresponding indoor levels (ranging from 36 to 68 μg/m³, p < 0.001), but significantly lower than outdoor levels (ranging from 43 to 95 μg/m³, p < 0.001). Indoor and outdoor PM₂.₅ concentrations were the strongest determinants of personal exposures in both cities and seasons, with RM² ranging from 0.814 to 0.915 for indoor and from 0.698 to 0.844 for outdoor PM₂.₅ concentrations, respectively. The personal-outdoor regression slopes varied widely among seasons, with a pronounced effect in BJ (NHS: 0.618 ± 0.042; HS: 0.834 ± 0.023). Ventilation status, indoor PM₂.₅ sources, personal characteristics, and meteorological factors, were also found to influence personal exposure levels. The city and season-specific models developed here are able to account for 89%–93% of the variance in personal PM₂.₅ exposure. A LOOCV analysis showed an R² (RMSE) of 0.80–0.90 (0.21–0.36), while a 10-fold CV analysis demonstrated a R² (RMSE) of 0.83–0.90 (0.20–0.35). By incorporating potentially significant determinants of personal exposure, this modeling approach can improve the accuracy of personal PM₂.₅ exposure assessment in epidemiologic studies.