Lake Hallstättersee is a holomictic alpine lake, which is influenced by salt mining since the middle Bronze Age. Beside the constant saline waste water load, two massive brine spills loaded the lake with additional 16,900 tons sodium chloride (≈10,250 tons Cl−) from 1977 to 1979 and 3,000 tons salt (≈1,820 tons Cl−) in 2005. The effect of waste water intrusions from salt mining on stratification of Lake Hallstättersee was analysed over a period of 40 years. Water density, dissolved oxygen and total phosphorus (TP) concentrations were measured and an exponential model was fitted to describe the wash-out of chloride from Lake Hallstättersee after the brine spills. Furthermore, the time required returning to holomixis and steady chloride content after the second brine spill was estimated. During the whole sampling period the minimum and maximum volume-weighted annual mean chloride concentrations were 23.58 mg/L in 1979 and 3.19 mg/L in 1998. However, the mixing regime of Lake Hallstättersee, as well as the chloride concentrations, varied considerably and exhibited three holomictic and three meromictic periods between 1970 and 2009. Holomictic periods were observed when the yearly density gradient was below 0.06 kg/m3, deepwater oxygen in spring above 4 mg/L and consequently declining TP concentration in the deepest water layer below 60 mg/m3, otherwise meromictic periods were observed. Our study showed that Hallstättersee was 13 years ectogenic meromictic and 27 years holomictic during the study period.

Poorly constructed wells (leaky or without a gravel pack) and abandoned wells can behave as conduits for the interconnection of aquifers at different depths and facilitate the transfer of contaminants between these aquifers. This is the case with Campo de Cartagena (SE Spain) where the primary land use is intensive irrigated agriculture, along with a high density of wells. The unconfined aquifer is heavily impacted by a high concentration of nitrate associated with agricultural activities. The present work provides a methodological approach to evaluate the impact of the unconfined aquifer on the water quality of the confined aquifer caused by leaky wells in high-density areas of production wells. The research approach included the use of geochemical and isotopic tools; specifically, nitrate was used as a tracer for evaluating the impact, and the code MIX_PROGRAM was used for mixing calculations. Results show an increase of the impact of the unconfined aquifer on the confined aquifer along the groundwater flow direction toward the coast, although this general pattern is controlled by local factors (pumping, intensity of agricultural practices, density of wells, and groundwater residence time).

The adsorption of lead onto date palm fibers (palm fibers) and leaf base of palm (petiole) has been examined in aqueous solution by considering the influence of various parameters such as contact time, solution pH, adsorbent dosage, particle sizes, ionic strength, and temperature. The adsorption of Pb(II) increased with an increase of contact time. The optimal range of pH for Pb(II) adsorption is 3.0-4.5. The linear Langmuir and Freundlich models were applied to describe the equilibrium isotherms, and both models fitted well. The monolayer adsorption capacity of Pb(II) on palm fibers and petiole was found as 18.622 and 20.040 mg/g, respectively, at pH 4.5 and 25°C. Dubinin-Radushkevich (D-R) isotherm model was also applied to equilibrium data. The mean free energy of adsorption (2.397 and 4.082 kJ/mol) onto palm fibers and petiole, respectively, may be carried out via physisorption mechanism. Pseudo-first-order rate equation and pseudo-second-order rate equation were applied to study the adsorption kinetics. In comparison to first-order kinetic model, pseudo-second-order model described well the adsorption kinetics of Pb(II) onto palm fibers and petiole from aqueous solution. From the results of the thermodynamic analysis, Gibbs free energy ΔG, enthalpy change ΔH, and entropy ΔS were determined. The positive value of ΔH suggests that interaction of Pb(II) adsorbed by palm fibers is endothermic. In contrast, the negative value of ΔH indicates that interaction of Pb(II) ions by petiole is exothermic. The negative value of ΔG indicates that the adsorption of Pb(II) ions on both palm fibers and petiole is a spontaneous process.

Nitrogen fertilizers used in agriculture often cause nitrate leaching towards shallow groundwater, especially in lowland areas where the flat topography minimize the surface run off. In order to introduce good agricultural practices that reduce the amount of nitrate entering the groundwater system, it is important to quantify the kinetic control on nitrate attenuation capacity. With this aim, a series of anaerobic batch experiments, consisting of loamy soils and nitrate-contaminated groundwater, were carried out using acetate and natural dissolved organic matter as electron donors. Acetate was chosen because it is the main intermediate species in many biodegradation pathways of organic compounds, and it is a suitable carbon source for denitrification. Sorption of acetate was also determined, fitting a Langmuir isotherm in both natural and artificially depleted organic matter soils. Experiments were performed in quadruplicate to account for the spatial variability of soil parameters. The geochemical code PHREEQC (version 2) was used to simulate kinetic denitrification using Monod equation, equilibrium Langmuir sorption of acetate, and equilibrium reactions of gas and mineral phases (calcite). The reactive modeling results highlighted a rapid acetate and nitrate mineralization rate, suggesting that the main pathway of nitrate attenuation is through denitrification while calcite acted as a buffer for pH. However, in the absence of acetate, the natural content of organic matter did not allow to complete the denitrification process leading to nitrite accumulation. Reactive modeling is thought to be an efficient and robust tool to quantify the complex biogeochemical reactions which can take place in underground environments.

Sulphuric acid-modified bagasse has been used as low-cost adsorbent for the removal of methylene blue (MB) dye from aqueous solution. In order to remove organic compounds that contribute to chemical oxygen demand (COD), pretreatment with thorough washing of adsorbent using boiling distilled water was performed instead of conventional washing using distilled water at room temperature only. This has resulted in the highest efficiency of color removal of 99.45% and COD reduction of 99.36% for MB dye solution at pH 9. Effects of initial pH, dye concentration, adsorbent dosage, temperature, and contact time have been studied. The adsorption of MB dye was pH dependent. Langmuir and Freundlich isotherm models were tested on the adsorption data. The kinetic experimental data were analyzed using pseudo-first order, pseudo-second order, and the intraparticle diffusion model in order to examine the adsorption mechanisms. The adsorption process followed the Langmuir isotherm as well as the Freundlich isotherm and pseudo-second-order kinetic model. The process was found to be endothermic in nature.

Among the most extensively used compounds for the pest control in Argentinean crops is the organochlorine endosulfan. The sublethal effects of the commercial endosulfan formulation on hematology and lipid peroxidation (LPO) of the neotropical fish Prochilodus lineatus were investigated. Firstly, we calculated acute toxicity (LC50) in order to define sublethal concentrations (0, 1.2, and 2.4 μg L−1). Hematological and oxidative stress responses were assessed at 24, 48, and 96 h. Endosulfan exposure significantly diminished the hemoglobin concentration, mean cell hemoglobin, and total plasma protein and increased white blood cells count and plasma glucose after 96 h. Exposed fish showed an alteration of the differential leukocytes count, evidenced by more thrombocytes and monocytes and less lymphocytes and neutrophils. Endosulfan increased LPO levels in intestine, liver, and brain in both sublethal concentrations. The present results suggest that endosulfan produces biochemical and physiological alterations, including immunological disorders, and it is a good inductor of oxidative stress in P. lineatus.

Surface coastal sediments (0–10 cm) collected from three natural environments on the Spanish Northern Atlantic Coast were analyzed so as to determine concentrations of 6 marker polychlorinated biphenyls (PCBs), 12 dioxin-like PCBs (dl-PCBs) and 17 polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs). An analytical procedure based on Soxhlet extraction followed by an automated cleanup and final high-resolution gas chromatography coupled to high-resolution mass spectrometry was applied for the determination of the persistent organic pollutants. Marker PCB levels ranged from 385.5 to 4,060.9 pg/g dry weight (d.w.) showing a similar congener pattern in all sediments dominated by the less volatile congeners PCB 153 and PCB 138. Linear correlations were found between marker and dl-PCBs. Toxicity equivalent values were calculated for PCDD/Fs and dl-PCBs reaching its maximum at 0.52 pg WHO1998-TEQ/g d.w., with an average dl-PCBs contribution on the toxicity of the samples of 75%, and showing to be in good agreement with background levels in the North-East Atlantic Ocean Coasts of nearly 1 pg/g WHO1998-TEQ d.w. Dimensionless environmental quality criteria were much lower than 1 indicating the low probability to induce ecotoxicological impacts.

In the present investigation, treatment of metal cutting wastewater (MCW) using electrocoagulation (EC) process is designed and analyzed using response surface methodology (RSM). RSM is applied to optimize the operating variables viz. initial pH, current density, and operating time on the treatment of MCW in a batch mode by EC process using iron and aluminum electrodes. Quadratic models are developed for the responses such as chemical oxygen demand (COD), total organic carbon (TOC), and turbidity, and operating cost is calculated with respect to energy, electrode, and chemical consumptions. The actual COD, TOC, and turbidity removal efficiencies at optimized conditions are found to be 93.0%, 83.0%, and 99.8% for Fe electrode and 93.5%, 85.2%, and 99.9% for Al electrode, respectively, which agree well with the predicted response. The proposed model fits very well with the experimental data with R 2 adjusted correlation coefficients of 0.927 for COD, 0.924 for TOC, and 0.968 for turbidity removal for Al and 0.904 for COD, 0.976 for TOC, and 0.989 for turbidity removal for Fe electrodes, respectively. This study clearly shows that RSM is one of the suitable methods to optimize the operating conditions and maximize the COD, TOC, and turbidity removal efficiencies for both electrodes while keeping the operating costs to minimal (0.371 <euro>/m3 for Fe and 0.337 <euro>/m3 for Al electrodes).

In order to evaluate fixation potential of schwertmannite for fluvial transport of various toxic elements, we examined bottom precipitates and stream waters collected from the rivers contaminated with acid mine drainage (AMD), which arose from the abandoned Nishinomaki mine (Shimonita, Gunma, Japan). Mineralogical and morphological observations revealed that schwertmannite was the main mineral of the precipitates. The affinity of various toxic ions to schwertmannite was evaluated on the basis of (1) apparent solid–liquid partition coefficients (K d’s) between precipitates and stream waters, (2) coprecipitation behaviors during schwertmannite formation in a laboratory test, and (3) consideration on coprecipitation processes using partial charge model (PCM). As a result, oxyanions of V, As, Mo and Sb, K d’s of which were relatively large (>104 (ml g−1)), were considered to be immobilized by schwertmannite precipitates. A laboratory test also demonstrated that these ions except Mo coprecipitated with schwertmannite. In addition, partial charges and average electronegativities predicted on the basis of PCM suggested that the oxyanions of V, As, Mo, and Sb could create stable inner sphere complexes with schwertmannite embryos, which results in their high affinity to schwertmannite. On the other hand, cationic ions of Mn, Cu, Zn, Sr, Cs, and U, K d’s of which were relatively small (<104 (ml g−1)), were thought to have a tendency to flow downstream without uptake by schwertmannite precipitates. All these results suggested that schwertmannite has high fixation potential for fluvial transport of various toxic oxyanions in AMD-contaminated rivers.

Two commercially available aerobic bioremediation methods (Daramend® and BioSan) were utilized to study the aerobic biodegradation of polycyclic aromatic hydrocarbons (PAH) and the effect of the simultaneously present arsenic. The soil was collected at an old wood preservation site, and the initial PAH₁₆-concentration was 46 mg/kg, with mainly high molecular weight congeners. The As concentration was 105 mg/kg with low availability as assessed with sequential extraction. To enhance the availability of PAH, the effect of a nonionic surfactant was evaluated. Degradation of both low and high molecular weight PAH was observed; however, after 30 weeks, the degradation was generally low and no treatment was significantly better than the others. The treatments had, on the other hand, an effect on As remobilization, with increased As concentration in the available fraction after treatment. This may be due to both the microbial activity and the presence of anoxic microsites in the soil. The overall efficiency of the biological treatment was further evaluated using the standardized ecotoxicity test utilizing Vibrio fischeri (Microtox®). The toxicity test demonstrated that the bioremediation led to an increase in toxicity, especially in treatments receiving surfactant. The surfactant implied an increase in contaminant availability but also a decrease in surface tension, which might have contributed to the overall toxicity increase.