Long-term irrigation with recycled water (RW) that contains high salt may pollute groundwater. The HYDRUS-1D model was texted against soil water content and electrical conductivity (ECe) observed in a summer maize and winter wheat rotational field irrigated with ground water (GW) and RW; then, the risk for polluting groundwater in two regions of Beijing was evaluated. The comparisons indicated that the simulated soil water content and ECe values were generally in agreement with the field observations, indicating the reliability of HYDRUS-1D in soils irrigated with GW and RW. The regional prediction results of the proposed simulation model indicated that the average soil ECe at the bottom of vadose zones ranged from 0.400 to 0.896 dS m⁻¹, and the values in the Tongzhou and Daxing Districts irrigated with RW were 1.40 and 1.09 times, respectively, higher than that irrigated with GW over the next 50 years. Five risk indicators represent salt transporting time and values were used. The results of the proposed evaluation model showed that the risk scores ranged from 3.04 to 9.32. In the Tongzhou and Daxing Districts, the risk scores of RW irrigation for polluting groundwater were 1.06 and 1.08 times, respectively, higher than that GW irrigation. The risk scores of GW or RW irrigation for polluting groundwater in the Tongzhou District were 1.75 or 1.72 times, respectively, higher than that in the Daxing District. Considering the small risk difference between GW and RW irrigations, RW can be used in both regions. Due to the different vadose zone structures, the Daxing District is more suitable for RW irrigation. The long-term use of RW for irrigation should consider the salt content of RW and vadose zone structure.

The competitive/simultaneous adsorption of arsenite (As(III)) and arsenate (As(V)) onto ferrihydrite is one of main processes controlling the distribution of arsenic under oxidizing conditions in the natural environment. Adsorption reactions of As(III) and As(V) with ferrihydrite were investigated by employing a combination of batch adsorption experiments and Fourier transform infrared (FTIR) spectroscopy measurements in single and binary systems, i.e., both As species were present at the same time. Isotherm studies showed that the adsorption of As(III) in the binary system was less than that in single system, indicating that As(V) hindered As(III) adsorption. The presence of As(III) had almost no impact on As(V) adsorption at pH 5 in the binary systems. Freundlich model described the equilibrium data well (R ² > 0.94), and the adsorption affinity onto ferrihydrite was in the following order: As(III)-single > As(III)-binary > As(V)-single > As(V)-binary. Kinetic data of As(III) and As(V) from single and binary systems were both well described by pseudo-second-order equation (R ² > 0.98). FTIR showed that after adsorbing of either As species, a new peak occurred at 826 cm⁻¹ due to the formation of Fe-O-As bonds, indicating that competition between As(III) and As(V) could take place on the surface sites as a result of the formation of a similar surface complexes.

In this study, the decolorization of a dye solution via bio-Fenton process with in situ generation of H₂O₂ by enzymatic catalyzed oxidation of glucose was investigated. For this purpose, magnetite was synthesized and was used as the support for glucose oxidase immobilization. The particle size of the magnetite was estimated to be around 42 nm according to the obtained scanning electron microscope images. The magnetite crystal size was obtained approximately 26 nm by X-ray diffraction spectrum. Effective variables on immobilization were investigated. The best immobilization conditions were achieved at pH 6, temperature of 10 °C, glucose oxidase/support ratio of 1800 U/g, and time of 2.5 h. In these conditions, 450 U of glucose oxidase was immobilized per grams of magnetite. The immobilized glucose oxidase was used for the decolorization of acid yellow 12 in batch experiments. Decolorization conditions were optimized by response surface methodology. Four parameters including pH, temperature, glucose, and Fe²⁺ concentrations in five levels were investigated. The optimum conditions were obtained as follows: pH = 4.5, T = 29 °C, initial glucose concentration of 1.5 g/L, and Fe⁺² concentration of 1.4 g/L. Decolorization efficiency after 120 min at optimal conditions in the presence of 0.3 g immobilized enzyme (450 U/g) in 100 cm³ solution was observed to be equal to 62.27 %.

Lead (Pb) has progressively become a widespread contaminant in the environment because of its intensive use and inherent stability. The contamination of Pb in agricultural soils is a major environmental problem. This paper considers the use of weathered coal humic acids for in situ remediation of Pb-contaminated soils. The effectiveness of acid rain on leaching in soil column was investigated. To determine the mobility and availability of Pb, we also investigated the soil pH and available soil Pb content from different depths in addition to the leachate pH and Pb concentrations at different times. Weathered coal has the potential to adjust the soil pH and leachate pH through metal-bridging mechanisms and deprotonation processes. We found that weathered coal humic acid and simulated acid rain significantly decreased the available surface soil Pb concentrations. The decrease in the available Pb concentrations in the surface layers of the soil was related to a significant increase in the available Pb concentrations in the middle layers of the soil. The application of weathered coal humic acid could reduce the Pb concentration of soil leachates. The removal of Pb was efficient, particularly at the 1000-mg-kg⁻¹ Pb pollution level, with a maximum decrease of 85.8 %.

Detecting and separating specific effects of contaminants in a multi-stress field context remain a major challenge in ecotoxicology. In this context, the aim of this study was to assess the usefulness of a non-invasive transcriptomic method, by means of a complementary DNA (cDNA) microarray comprising 1000 candidate genes, on caudal fin clips. Fin gene transcription patterns of European eels (Anguilla anguilla) exposed in the laboratory to cadmium (Cd) or a polychloro-biphenyl (PCBs) mixture but also of wild eels from three sampling sites with differing contamination levels were compared to test whether fin clips may be used to detect and discriminate the exposure to these contaminants. Also, transcriptomic profiles from the liver and caudal fin of eels experimentally exposed to Cd were compared to assess the detection sensitivity of the fin transcriptomic response. A similar number of genes were differentially transcribed in the fin and liver in response to Cd exposure, highlighting the detection sensitivity of fin clips. Moreover, distinct fin transcription profiles were observed in response to Cd or PCB exposure. Finally, the transcription profiles of eels from the most contaminated site clustered with those from laboratory-exposed fish. This study thus highlights the applicability and usefulness of performing gene transcription assays on non-invasive tissue sampling in order to detect the in situ exposure to Cd and PCBs in fish.

The objective of this study was to assess the impact of metal contamination on microbial functional diversity and enzyme activity in forest soils. This study involved the evaluation of the influence of the texture, carbon content and distance to the source of contamination on the change in soil microbial activity, which did not investigate in previous studies. The study area is located in southern Poland near the city of Olkusz around the flotation sedimentation pond of lead and zinc at the Mining and Metallurgical Company “ZGH Bolesław, Inc.”. The central point of the study area was selected as the middle part of the sedimentation pond. The experiment was conducted over a regular 500 × 500-m grid, where 33 sampling points were established. Contents of organic carbon and trace elements (Zn, Pb and Cd), pH and soil texture were investigated. The study included the determination of dehydrogenase and urease activities and microbial functional diversity evaluation based on the community-level physiological profiling approach by Biolog EcoPlate. The greatest reduction in the dehydrogenase and urease activities was observed in light sandy soils with Zn content >220 mg · kg⁻¹ and a Pb content > 100 mg · kg⁻¹. Soils with a higher concentration of fine fraction, despite having the greatest concentrations of metals, were characterized by high rates of Biolog®-derived parameters and a lower reduction of enzyme activity.

We measured the concentrations of dissolved inorganic nitrogen (DIN; nitrate, ammonium, and nitrite) in stream water in a paddy-dominated agricultural basin in a snowfall area from August 2009 to October 2010 to facilitate evaluation of stream water eutrophication from nitrogen during the non-irrigated period. We compared the nitrogen budget in a paddy field between irrigated and non-irrigated periods, from information about nitrogen fertilizer, denitrification, harvested rice, and atmospheric nitrogen deposition. We also estimated stream nitrogen exports from DIN concentrations and stream flow rates. DIN concentrations in stream water were higher during the non-irrigated period (October–March) than during the irrigated period (April–September). Stream flow was also higher during the non-irrigated period (5.9 mm day⁻¹) than during the irrigated period (2.5 mm day⁻¹), which possibly reflects snow melting. Although nitrogen fertilizer was applied during the irrigated period, the amount of nitrogen removed by the rice harvest and denitrification was sufficiently large to reduce nitrogen exports from paddy fields. Atmospheric nitrogen deposition was higher during the non-irrigated period (755 kg N km⁻²) than during the irrigated period (410 kg N km⁻²). DIN exports were also higher in the non-irrigated period (860 kg N km⁻²) than in the irrigated period (120 kg N km⁻²). The higher exports in the non-irrigated period may reflect the lack of nitrogen removal by a rice harvest and denitrification and increased runoff and higher atmospheric nitrogen deposition. Our study highlights the important contribution of the non-irrigated period to nitrogen eutrophication in stream water in this particular environment.

Microcystis aeruginosa is a common cause of algal bloom outbreaks in Chinese lakes. This study investigated the effects of phosphate loading on the algal growth and extracellular organic matter (EOM) production of M. aeruginosa. The cell density was monitored by cell counting, and EOMs were characterized by dissolved organic carbon (DOC), carbohydrate, protein, and excitation/emission matrix fluorescence spectroscopy (EEM). DOC concentration peaked during the stationary phase and was contributed primarily by amino acid- and fulvic-like substances. Carbohydrate was a substantially larger fraction than protein. Phosphate showed positive influence on the cell growth and EOMs. As its concentration increased, the EOMs concentration increased. So did EOM and β-ionone as typical taste and odor compounds. Whatever the phosphate concentration was, the peak of β-ionone concentration exceeded its odor threshold (7.0 ng/L), resulting in a severe fruit-like odor. Additionally, the disinfection by-products involved with EOM were evaluated in both chlorination and chloramination, indicating that trihalomethanes were the dominated toxic by-products and the chloramination showed more significant effect on its formation as an interesting result.

Pilot scale thin film plate reactors (TFPR) were fabricated to study the solar photocatalytic treatment of wastewater obtained from the secondary treatment plant of a sugar refinery. Silver-impregnated titanium dioxide (TiO₂) was prepared by a facile chemical reduction method, characterized, and immobilized onto the surface of ceramic tiles used in the pilot scale reactors. On 8 h of solar irradiation, percentage reduction of chemical oxygen demand (COD) of the wastewater by Ag/TiO₂, pure TiO₂, and control (without catalyst) TFPR was about 95, 86, and 22 % respectively. The effects of operational parameters such as, flow rate, pH, and addition of hydrogen peroxide (H₂O₂) were optimized as they influence the rate of COD reduction. Under 3 h of solar irradiation, 99 % COD reduction was observed at an optimum flow rate of 15 L h⁻¹, initial pH of 2, and addition of 5 mM of H₂O₂. The results show that Ag/TiO₂ TFPR could be effectively used for the tertiary treatment of sugar refinery effluent using sunlight as the energy source. The treated water could be reused for industrial purposes, thus reducing the water footprint of the industry. Graphical Abstract Sugar refinery effluent treatment by solar photocatalytic TFPR

The chemical reduction of hexavalent chromium (Cr(VI)) by combined zerovalent magnesium (ZVMg) and ultrasound (US) was studied under batch conditions. Results have demonstrated that the reduction of Cr(VI) mediated by ZVMg enhanced significantly with the ultrasonic effect. The percent reduction of Cr(VI) by ZVMg (5 g/L) was about 20 % after 60 min, but its complete reduction was attained within an hour when ultrasound was applied at a power of 100 W. The efficiency of Cr(VI) reduction increased with increasing ultrasonic power and magnesium dose. The synergy of the combined treatment has been attributed to the surface activation of ultrasonic treatment. Scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), atomic absorption spectrophotometer (AAS), pH, and X-ray diffraction (XRD) analyses have revealed that magnesium and chromium hydroxides and hydroxide ion were three major by-products during the reduction of Cr(VI) by US/ZVMg under pH-uncontrolled conditions. The proposed method does not require acid and buffer addition and has an advantage of removing Cr(VI) and its by-product (Cr(III)) simultaneously.