Recycled materials were used in three types of green sorption media for nutrient removal and possible recovery in high nutrient-laden agricultural discharge and stormwater runoff. The three types of green sorption media included in this comparative study were two new aluminum-based green environmental media (AGEM) and one existing iron-filings based green environmental media (IFGEM). The corresponding adsorption isotherm, thermodynamics, and kinetics models were simulated based on isotherm studies to determine their removal efficiency and potential for recovery of nitrate, phosphate, and ammonia when used as a soil amendment in crop fields or in a filter for water treatment. AGEM-2 exhibited the shortest contact time required to achieve nutrient removal above 80% with an average of 7 h, followed by AGEM-1 and IFGEM with 10.6 and 28 h, respectively. Natural soil was included as a control and exhibited minimal nutrient removal. Ammonia, which may be recovered as fertilizer for drop fields in a soil-water-waste nexus, was generated by all three green sorption media mixes, therefore indicating their potential for use as soil amendments in agricultural and forested land after engineering filter applications. The kinetics analysis indicated that nitrate adsorption follows pseudo-first-order kinetics, while phosphate adsorption follows pseudo-second-order kinetics. The Gibbs free energy indicated that most of the adsorption reactions proceeded as exothermic. Lastly, a few equilibrium models, including the Langmuir, Freundlich, First Modified Langmuir, Temkin, Jovanovic, and Elovich models, were ranked and three were selected for use with IFGEM, AGEM-1, and AGEM-2, respectively, as below: (1) Langmuir, (2) Freundlich, and (3) First Modified Langmuir, according to three indices.

PFASs are highly persistent in both natural and living environment, and pose a significant risk for wildlife and human beings. The present study was carried out to determine the inhibitory behaviours of fourteen PFASs on metabolic activity of two major isoforms of carboxylesterases (CES). The probe substrates 2-(2-benzoyl-3-methoxyphenyl) benzothiazole (BMBT) for CES1 and fluorescein diacetate (FD) for CES2 were utilized to determine the inhibitory potentials of PFASs on CES in vitro. The results demonstrated that perfluorododecanoic acid (PFDoA), perfluorotetradecanoic acid (PFTA) and perfluorooctadecanoic acid (PFOcDA) strongly inhibited CES1 and CES2. The half inhibition concentration (IC₅₀) value of PFDoA, PFTA and PFOcDA for CES1 inhibition was 10.6 μM, 13.4 μM and 12.6 μM, respectively. The IC₅₀ for the inhibition of PFDoA, PFTA and PFOcDA towards CES2 were calculated to be 9.56 μM, 17.2 μM and 8.73 μM, respectively. PFDoA, PFTA and PFOcDA exhibited noncompetitive inhibition towards both CES1 and CES2. The inhibition kinetics parameters (Kᵢ) were 27.7 μM, 26.9 μM, 11.9 μM, 4.04 μM, 29.1 μM, 27.4 μM for PFDoA-CES1, PFTA-CES1, PFOcDA-CES1, PFDoA-CES2, PFTA-CES2, PFOcDA-CES2, respectively. In vitro-in vivo extrapolation (IVIVE) predicted that when the plasma concentrations of PFDoA, PFTA and PFOcDA were greater than 2.77 μM, 2.69 μM and 1.19 μM, respectively, it might interfere with the metabolic reaction catalyzed by CES1 in vivo; when the plasma concentrations of PFDoA, PFTA and PFOcDA were greater than 0.40 μM, 2.91 μM, 2.74 μM, it might interfere with the metabolic reaction catalyzed by CES2 in vivo. Molecular docking was used to explore the interactions between PFASs and CES. In conclusion, PFASs were found to cause inhibitory effects on CES in vitro, and this finding would provide an important experimental basis for further in vivo testing of PFASs focused on CES inhibition endpoints.

Short-chain chlorinated paraffin (SCCP) concentrations in 419 food samples (from 59 species) from Republic of Korea were determined. The SCCP concentrations and lipid contents in whole foods positively correlated and the highest SCCP concentration (891 ng/g wet weight) was observed in fats and oils. The SCCP concentrations were higher in benthic fish/shellfish and demersal fish than other fish and shellfish. The SCCP concentrations were higher in duck meat and eggs than meat and eggs of other species. The chlorine-based congener group patterns were related to the lipid contents of the foods. SCCPs in eggs (high lipid content) were dominated by more-chlorinated SCCPs (particularly Cl₈-SCCPs, which contributed 43% of the total) but SCCPs in seaweed (low lipid content) were dominated by less-chlorinated SCCPs (particularly Cl₆-SCCPs, which contributed 46%). Dietary SCCP intakes were calculated using the median SCCP concentrations and estimated 888 and 781 ng/kg/d for male and female Korean adults, respectively. The predominant contributing foods to SCCP dietary exposure differed according to sex and age. Dairy products contributed most (about 50%) for infants/children (1–5 y old), but meat and dairy products contributed most for adult males and females, respectively. Grain contributed most for ≥65 y old.

In the last decade many studies have described the ingestion of plastic in marine animals. While most studies were dedicated to understanding the pre-ingestion processes involving decision-making foraging choices based on visual and olfactory cues of animals, our knowledge in the post-ingestion consequences remains limited. Here we proposed a theoretical complementary view of post-ingestion consequences, attempting to connect plastic ingestion with plastic-induced satiety. We analyzed data of plastic ingestion and dietary information of 223 immature green turtles (Chelonia mydas) from tropical Brazilian reefs in order to understand the impacts of plastic ingestion on foraging behavior. Generalized linear mixing models and permutational analysis of variance suggested that plastic accumulations in esophagus, stomach and intestine differed in their impact on green turtle’s food intake. At the initial stages of plastic ingestion, where the plastic still in the stomach, an increase in food intake was observed. The accumulation of plastic in the gastrointestinal tract can reduce food intake likely leading to plastic-induced satiety. Our results also suggest that higher amounts of plastics in the gastrointestinal tract may led to underweight and emaciated turtles. We hope that adopting and refining our proposed framework will help to clarify the post-ingestion consequences of plastic ingestion in wildlife.

Emissions of major reactive nitrogen compounds, including nitric oxide (NO), nitrogen dioxide (NO₂) and ammonia (NH₃), from heavy-duty diesel vehicles (HDDVs) place substantial pressure on air quality for many large cities in China. To control nitrogen oxide (NOX) emissions from HDDVs, selective catalytic reduction (SCR) systems have been widely used since the China IV standards. To investigate the impacts of aftertreatment technologies and driving conditions on real-world emissions of reactive nitrogen compounds, a portable emissions measurement system was employed to test eighteen heavy-duty diesel trucks in China. The results showed that the China IV and China V HDDVs with appropriate SCR functionality could reduce NOX emissions by 36% and 53%, respectively, compared to the China III results, although their real-world emissions were still higher than the corresponding emission limits for regulatory engine tests. For these HDDVs, five samples were tested with NH₃ emissions, ranging from 1.67 ppm to 51.49 ppm. The NH₃ emission rates tended to significantly increase under high-speed driving conditions. The results indicate that the current SCR technology may have certain risks in exceeding the future China VI NH₃ limit. However, five China IV/V HDDVs were found to have SCR temperature sensors that were intentionally tampered with, resulting in comparable or even higher NOX emissions and zero NH₃ emissions. Increased NO₂ emissions due to the adoption of diesel oxidation catalysts and diesel particulate filters were also found from our experiments. This study highlights the importance of enhancing in-use compliance requirements and eliminating aftertreatment tampering for China IV and China V HDDVs.

There has been a growing concern with the environmental influences of nanomaterials due to recent developments in nanotechnology. This study investigates the impact and fate of hematite nanoparticles (α-Fe₂O₃ NPs) (∼14 nm in size) on a crop species, barley (Hordeum vulgare L.). For this purpose, hematite NPs (50, 100, 200, and 400 mg/L) were hydroponically applied to barley at germination and seedling stages (three weeks). Inductively coupled plasma mass spectrophotometry (ICP-MS) along with vibrating sample magnetometer (VSM) techniques were used to track the NPs in plant tissues. The effects of NPs on the root cells were observed by scanning electron microscopy (SEM) and confocal microscopy. Results revealed that α-Fe₂O₃ NPs significantly reduced the germination rate (from 80% in control to 30% in 400 mg/L), as well as chlorophyll (36–39%) and carotenoid (37%) contents. Moreover, the treatment led to a significant decline in the quantum yield of photosystem II (Fv/Fm). Leaf VSM analysis indicated a change in magnetic signal for NPs-treated samples compared with untreated ones, which is mostly attributed to the iron (Fe) ions incorporated within the leaf tissue. Besides, Fe content in the roots and leaf had gradually increased by the increasing doses of NPs, which was confirming NPs’ translocation to the aerial parts. Microscopic observations revealed that α-Fe₂O₃ NPs altered root cell morphology and led to the injury of cell membranes. This study, in the light of our findings, shows that α-Fe₂O₃ NPs (∼14 nm in size) are taken up by the roots of the barley plants, and migrate to the plant leaves. Besides, NPs are phytotoxic for barley as they inhibit germination and pigment biosynthesis. This inhibition is probably due to the injury of the cell membranes in the roots. Therefore, the use of hematite NPs in agriculture and thereby their environmental diffusion must be addressed carefully.

Traditional toxicity tests assess stressor effects on individuals, while protection goals are focused on the population-level and above. Additionally, these tests ignore common ecological factors such as resource levels and population growth phase. The objective of this research was to explore effects of – and interactions between – resource availability and stress response at the individual and population levels using Daphnia magna as a model. We hypothesized that density-dependent changes in resources at various phases of population growth would cause different population responses to the same toxicant stress. Laboratory populations of Daphnia magna were exposed to a 48-h pulse of 20 or 30 μg/l pyraclostrobin in one of four distinct phases of laboratory population cycles: growth, peak, decline, and stable. Population size and recovery were observed throughout the 51-day study. Populations exposed to pyraclostrobin during the growth phase had the least mortality and fastest recovery, while populations in the peak phase had the greatest mortality and slowest recovery. These data suggested that high density and low food at the peak phase resulted in more sensitive daphnids. To further test this hypothesis, a resource-amended acute toxicity study was conducted to quantify the effects of food resource on pyraclostrobin toxicity to Daphnia magna. Three age classes of Daphnia magna (neonate, subadult, adult) were fed low or high food levels and exposed to pyraclostrobin for 48 h. Toxicity was greater, as shown by lower 48 h LC50s, for smaller Daphnia magna age classes and lower food levels comporting results in the population study. Importantly, the acute toxicity studies generally yielded lower effect levels than the population studies suggesting that while the standard acute studies are ecologically unrealistic, they may be protective of toxicity under some circumstances. Collectively, these data point to the importance of population phase and the resource environment in modulating toxicity.

Contamination by polycyclic aromatic hydrocarbons (PAHs) has been observed at high elevation environments; however, the occurrence and spatial variation of PAHs in alpine lakes of China is not well understood. We measured 15 priority PAHs in the sediments of Lake Qinghai in the Qinghai-Tibet Plateau, and assessed their distribution, source, and ecological risks. The total PAH concentration ranged from 30.4 to 125.2 ng g⁻¹. Low molecular weight PAHs were dominant in the sediments, suggesting a local source for the emissions. Sediment sites closer to local settlements and rivers had higher concentration of PAHs. The concentration of PAHs was significantly correlated with pH, probably as a result of the high salinity of the lake, while it was not significantly correlated with organic matter content. Molecular diagnostic ratio analysis indicated that PAHs were derived mainly from coal and biomass combustion. Specifically, the positive matrix factorization model showed that petrogenic sources, vehicular emissions, biomass combustion, and coal combustion contributed for 11.6, 16.3, 23.6, and 48.5% of the PAHs, respectively. The risk quotient method was used to assess ecological risk of PAHs individually. The results indicate that indeno[1,2,3-cd]pyrene, benzo[b]fluoranthene, benzo[a]pyrene, phenanthrene, and anthracene would produce moderate ecological risks in 5, 20, 65, 100, and 100% of the sediment sites, respectively, while the other 10 PAH homologues would scarcely produce any serious ecological risk. We used the hierarchical Archimedean copula integral assessment model to evaluate the integral risk of PAHs. The result showed that 10, 40, and 50% of the sediment sites belong to mid-high, low, and mid-low risk levels, respectively. The current concentration and risk levels of PAHs in this study might be used as a baseline to assess the influence of future anthropogenic activities.

Phytoextraction using Celosia argentea Linn. can potentially decontaminate Cd-contaminated soils. However, most earlier studies have been conducted at laboratory scale and for a relatively short remediation period. To evaluate the phytoextraction efficiency of C. argentea combined with different soil amendments (ammonium chloride, Bacillus megaterium, and citric acid), an 18-month field experiment was carried out in a farmland soil contaminated with 3.68 mg kg⁻¹ Cd by mine tailings in southern China. Soil Cd concentrations were decreased by 6.34 ± 0.73% after the three harvestings (with no amendments), which was 2.27 times that of the no-planting control (p < 0.05). Application of ammonium chloride, B. megaterium, and citric acid increased the overall Cd reduction rate in soil by 40.5%, 46.1%, and 105%, respectively. The application of citric acid decreased total Cd in soil by up to 16.9% in the rhizosphere soil and 13.0% in the bulk soil. The highest annual shoot biomass yield and Cd extraction amount reached 8.79 t ha⁻¹ and 273 g ha⁻¹. Acid-soluble Cd fraction in the rhizosphere was significantly lower compared to that in the bulk soil (p < 0.05), which indicates that mobile Cd in the rhizosphere was taken up by the roots vastly. C. argentea phytoextraction also improved soil metabolic functions by increasing the activities of soil enzymes (urease, invertase, phosphatase, and catalase). These findings demonstrate that Cd phytoextraction using C. argentea with the application of soil amendments can greatly improve the quality of Cd-contaminated soils.

A compound system involving three matrices (water, sediment, and paddy soil) was conceived to determine the potential sources of metal(loid)s (Ti, Fe, Co, Ni, Cu, Zn, As, Cd, Pb, and U) and synthetically evaluate their pollution levels in the Le’an River basin. The result indicated that the established background values (BVs) of paddy soil and sediment in the compound system were obviously higher than those of the upper continental crust (UCC) and soils from Jiangxi Province, a difference which was especially marked for sediment. The concentrations of Cu, Zn, As, Cd in the system had high coefficients of variation (CVs), and metal(loid)s in sediment showed higher levels than those in paddy soil, except for Pb. Cd and Cu in the system had the highest Ef levels, which probably pose a high risk to organisms and the health of local residents. There were significantly linear relationships between the site rank index (SRI) for water and that for sediment or paddy soil, revealing that matrices in the system interacted with each other. Principal component analysis (PCA) and absolute principal component scores and multiple linear regression model (APCS-MLR) results demonstrated that Cu, Zn, As, Cu, Pb, and U enrichments in the system were mainly affected by mining activities and were predominately deposited in sediment. Point pollution sources rather than non-point pollution sources such as mining activities, contributed most of the anthropogenic metal(loid)s to sediment. Both SRI and Hierarchical cluster analysis (HCA) results visually showed that S5, S8, S9, S10, S11, and S12 severe pollution grouped together and scattered through areas with extensive mining activities, while other sites with moderate pollution were spread along the main stream of the Le’an River.