The study presented here focuses on the use of monolayer covers for reclaiming two acid-generating tailings sites located in Quebec, Canada. One of these covers is made of non-acid-generating tailings, and the other is made of a silty sand (till). The covers are part of the closure plans that aim at controlling acid mine (rock) drainage at these two sites. Reactive tailings and cover material samples were collected in situ and characterised in the laboratory. Large-size columns (230 cm in height) were set up to evaluate the hydrogeological and geochemical response of the tailings and cover systems. Monthly wetting and drying cycles were repeated over nearly 2 years to simulate climatic conditions. Water content, suction, and oxygen concentrations were monitored, and chemical analyses were performed on the leachate collected at the base during each cycle to follow the evolution of water quality, in terms of pH and concentrations of sulfates and metals. In addition, small columns (45 cm in height) were also set up, with a similar testing program, to assess the hydrogeochemical behaviour of exposed tailings. The specific objective of this experimental program was to evaluate the hydrogeological and geochemical behaviour of the tailings-cover systems under controlled conditions. The results indicate that, for the imposed conditions, the monolayer covers became significantly desaturated, thus insufficiently limiting the oxygen diffusion flux. Consequently, these covers do not efficiently prevent sulfide oxidation within the tailings. The implications of these results are also discussed.

The influence of structure on degradation of five halogenated phenols (XPs) by UV/H₂O₂process was investigated. The combined influence of type or number of substituents and UV/H₂O₂process parameters (pH and [H₂O₂]) on the degradation kinetics of 2-fluorophenol (2-FP), 2-chlorophenol (2-CP), 2-bromophenol (2-BP), 2,4-dichlorophenol (2,4-DCP), and 2,4,6-trichlorophenol (2,4,6-TCP) was studied using modified miscellaneous 3³full factorial design and response surface modeling (RSM). Studied XPs obey first-order degradation kinetics within the investigated range of process parameters. Determined degradation rate constants (kₒbₛ) were correlated with process and structural parameters by the quadratic polynomial models. Analysis of variance (ANOVA) demonstrated RSM models’ accuracy and showed that, in addition to pH and [H₂O₂], model terms related with the pollutant structure are highly influential. kₒbₛof mono-XPs follow the decreasing order 2-FP, 2-CP, and 2-BP, while CPs follow the decreasing order 2-CP, 2,4-DCP, and 2,4,6-TCP. Biodegradability (biochemical oxygen demand (BOD)₅/chemical oxygen demand (COD)) and toxicity (TU) were evaluated prior to the treatment and at the reference time intervals. The observed differences are correlated with the structural characteristics of studied XPs.

This study evaluates the degree of pollution of marine sediments using two methods: standard (physico-chemical parameters) and instrumental techniques: thermogravimetric analysis (TG) and infrared spectroscopy (ATR-FTIR). ATR-FTIR proved to be a tool capable of identifying the organic and inorganic compounds in sediments such as organic carbon, clay, and carboxylate groups which can bind metal contaminants. TG results of 14 sediment samples were compared with organic matter (OM), organic carbon (OC), total nitrogen (TN), clay, and carbonate (CaCO₃) contents obtained by standard methods. The results showed that weight losses for a specific range of temperatures are closely correlated with the content of OM (R ² = 0.92), OC (R ² = 0.82), TN (R ² = 0.96), clay content (R ² = 0.87), and CaCO₃ (R ² = 0.9) for sediment samples. It is concluded that TG and ATR-FTIR allows a simultaneous, rapid, and reliable screening of sediment properties.

A nitrate-dominant synthetic wastewater simulating slightly polluted water with low C/N and poor biochemical availability was treated in lab-scale vertical-flow (VF)-constructed wetlands, which had Phragmites australis planted with different types of external carbon sources: Platanus acerifolia leaf litters, P. australis litters, glucose and a blank test with no external carbon sources. A comparison of the TN removal and N₂O flux performances among the four wetland reactors indicated higher TN removal efficiencies and N₂O release fluxes in the VF wetland columns with external carbon sources, as measured by the percentage removal of TN (P. acerifolia leaf litters 82.49 %, P. australis litters 70.55 %, glucose 62.50 % and blank 46.45 %) and N₂O flux (P. acerifolia leaf litters 2275.22 μg · m⁻² · h⁻¹, P. australis litters 1920.53 μg · m⁻² · h⁻¹, glucose 1598.57 μg · m⁻² · h⁻¹and blank 1192.08 μg · m⁻² · h⁻¹). This was primarily because of an improved supply of organic carbon from the external carbon sources for heterotrophic denitrification. And, the nitrogen released from the decomposition of plant materials resulted in the N₂O release fluxes to some extent. However, employing P. acerifolia leaf litters and P. australis litters as external carbon sources caused net increases in organics of the final effluent water. Overall, the results not only demonstrated the potential of using external plant carbon sources in VF wetlands to enhance the TN removal efficiency but also showed a risk of excessive organic release and greater N₂O flux feedback to global warming. Hence, future studies are needed to optimise the quantity and method for adding external carbon sources to VF-constructed wetlands so that sufficient nitrate removal efficiency is achieved and the N₂O flux and organic pollution are minimised.

Oil spills impose serious damage to the environment. A spilled crude oil or its products affect aquatic flora and fauna and influence the atmosphere as well. Such pollutants are especially dangerous for the water ecosystems, where biological self-purification processes are slower (for example the Baltic Sea), than in warmer regions. In this paper, we evaluate a sorption capacity of ecologically friendly natural sorbents, when the crude oil and diesel are spilled on the surface of water. The experiments are carried out in the laboratory, and the water from the Lithuanian Baltic Sea coastline and Curonian Lagoon is used. Moss, straw, wool, sawdust, and peat are the natural sorbents evaluated during the experiments. Chromatographic analysis of crude oil and diesel during the process of sorption was conducted as well. An experiment with some synthetic sorbents was carried out to compare the results with natural ones. The experiments showed that the most suitable material for crude oil or diesel fuel spilled on the water surface is peat. As well, Lagergren’s model was adopted to the case of the sorption processes we have investigated. It can be exploited as a decision support tool while deciding the required time interval to achieve maximum sorption capacity of the sorbent in use.

The present study was conducted to maximize the biosorption of dye by utilizing the native (untreated) pellets of Aspergillus lentulus. The native (55.0 mg/g) and heat-treated (56.7 mg/g) pellets showed excellent dye biosorption capacity which declined upon alginate immobilization (27.2 mg/g). Fourier transform infrared and EDX spectra revealed that phosphate and –CH₃groups are important in determining the biosorption capacity of the pretreated fungal biomass. The operating conditions of the aerated fed batch reactor were optimized and 90 % removal of Acid Blue 120 in 12 h was achieved after five biosorption–desorption cycles. At the end of the fifth cycle, 508.57 mg/L dye could be removed in 60 h with the removal rate of 8.48 mg/L/h. Further, the potential utilization of fungal biomass for the treatment of complex effluent was validated by studying the dye removal from unprocessed textile effluent wherein 58.0 % dye was removed within 4 h of contact.

Aluminium is used in diverse anthropogenic processes at the origin of pollution events in aquatic ecosystems. In the Champagne region (France), high concentrations of aluminium (Al) are detected due to vine-growing practices. In fish, little is known about the possible immune-related effects at relevant environmental concentrations. The present study analyzes the simultaneous effects of aluminium and bacterial lipopolysaccharide (LPS), alone and in combination, on toxicological biomarkers in the freshwater fish species Rutilus rutilus. For this purpose, roach treated or not with LPS were exposed to environmental concentrations of aluminium (100 μg/L) under laboratory-controlled conditions for 2, 7, 14 and 21 days. After each exposure time, we assessed hepatic lipoperoxidation, catalase activity, glutathione reductase activity and total glutathione content. We also analyzed cellular components related to the LPS-induced inflammatory response in possible target tissues, i.e. head kidney and spleen. Our results revealed a significant prooxidant effect in the liver cells and head kidney leukocytes of roach exposed to 100 μg of Al/L for 2 days. In liver, we observed more lipoperoxidation products and lower endogenous antioxidant activity levels such as glutathione reductase activity and total glutathione content. These prooxidant effects were associated with a higher oxidative burst in head kidney leukocytes, and they were all the more important in fish stimulated by LPS injection. These findings demonstrate that environmental concentrations of Al induce oxidative and immunotoxic effects in fish and are associated to an immunomodulatory process related to the inflammatory response.

Natural resource habitats, which are isolated from the surface water bodies, are often unregulated and face a higher risk of degradation. Vernal pools, habitats for amphibians, are vulnerable to external stressors that often lead to decline in biodiversity. There is a need to protect these through conservation measures at a spatially targeted level. This study is conducted in the Middle Connecticut River Watershed of Massachusetts State. We evaluate the risk faced by isolated vernal pools at the subwatershed scale. The assessment involves the impact of agricultural intensity and vernal pool distribution in proximity to agriculture parcels. This is performed using geoprocessing techniques within a geographic information system (GIS). The spatial data are used in a nonlinear regression model to evaluate potential stressors to vernal pool existence. The model included land use, geographic features, and hydrographic factors. Agriculture and open land positively influence vernal pool existence, because of vernal pool association with low-lying areas. In addition, elevation showed a negative influence on the number of vernal pool habitats. The results of the spatial risk evaluation of habitat are helpful to target efforts on specific subwatersheds in conserving vernal pool habitats.

A novel mesoporous, nanocomposite, magnetically separable adsorbent, namely activated alumina (γ-Al₂O₃)/ferrite (Ni₀.₅Zn₀.₅Fe₂O₄) microfibers have been successfully prepared by the sol–gel process. These nanocomposite γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers are formed after calcination of the precursor at 450 °C for 3 h, and characterized with high aspect ratios and uniform diameters of 1–10 μm. In the nanocomposite γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers, the spherical γ-Al₂O₃particles are homogeneously embedded on the microfiber. Their specific surface areas and magnetic properties are significantly influenced by the γ-Al₂O₃content and calcination conditions. With the designed γ-Al₂O₃mass fraction of 0.2 and the calcination temperature of 550 °C, the γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers possess a high specific surface area of 118.3 m²/g and saturation magnetization (Mₛ) of 20.4 Am² kg⁻¹, respectively. The adsorption behaviors of the nanocomposite γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers were examined using the Congo red and methyl blue dyes as the adsorbate. The adsorption kinetics, effects of the adsorbent dosage and solution pH, adsorption isotherms, and regeneration of the microfiber adsorbents were investigated. The pseudo-second-order model can be used to describe the adsorption kinetics. The resultant isotherm data are well fitted by the Temkin model, implying that the dyes adsorption on the γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers is a multilayer adsorption combined with some degrees of chemical interactions. Considering the simple synthesis process, high adsorption and unique magnetic property, these mesoporous, magnetic, nanocomposite γ-Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers can be used as a highly efficient, fast, and convenient adsorbent for dyes removal.Highlights The magnetic mesoporous Al₂O₃/Ni₀.₅Zn₀.₅Fe₂O₄microfibers were synthesized. Adsorption kinetics and adsorption isotherms were investigated. The separation, regeneration, and adsorption efficiency were enhanced.

Heavy metals are determinant factors in increasing environmental pollution, and chromium is considered to be of highest concern because of its genotoxicity in microorganisms, animals, and humans. Relatively few studies are focused on the injury induced in plant genetic material. Therefore, the main objective of this work was to evaluate the extent of the cytogenetic damage induced in root meristems of barley (Hordeum vulgare L.) after short-term seed exposure to 10, 100, 250, and 500 μM K₂Cr₂O₇(Cr(VI) concentration is 1.04, 10.39, 25.99, and 51.99 μg ml⁻¹) and 10, 100, 250, and 500 μM CrCl₃(Cr(III) concentration is 0.52, 5.19, 12.99, and 25.99 μg ml⁻¹). Chromium genotoxic potential was proved by significant increases in the rates of the ana-telophase chromosomal aberrations (1.3–2.3 times higher for K₂Cr₂O₇and 1.7–2.2 times higher for CrCl₃, as compared to the control; p < 0.05, p < 0.01) and of metaphase disturbances (5.0–7.5 times more numerous in chromium-treated groups than in control; p < 0.001). The pattern of the chromosomal aberrations is constituted by chromatid bridges, complex aberrations, lagging, and vagrant chromosomes, while the abnormal metaphases are c-like metaphases, sticky metaphases, and metaphases with chromosomes expulsed from equatorial plate. The mitotic indices and the growth of the barley plantlets in the early ontogeny were stimulated by chromium. The changes induced in the frequency of division stages mainly consisted in prophase and telophase accumulation and diminution of metaphase and anaphase proportion.