Mercury (Hg) bioaccumulation and depuration potential was assessed in the glass eel Anguilla anguilla over a 30-day period, through a mesocosm experiment. During exposure period, glass eels exhibited a significant increase in Hg concentration compared with the control ones, revealing great accumulation capability. Distinct bioaccumulation kinetics were observed depending on the exposure concentrations: a saturation model and a linear accumulation model were achieved for low and high Hg levels, respectively. After 72 h of depuration, glass eels lost around 2 and 10 % of the Hg previously accumulated; however, until the end of the experiment, they never reached the original baseline condition. Most importantly, organisms exposed to high Hg concentrations still retained contaminant levels exceeding the European threshold regulating human food consumption. This may raise serious health concerns, due to the species’ rising interest in the international cuisine.

Two lakes, one from the remote high altitude on the southern slope of the Himalaya (Lake Gosainkunda) and another from the urban mid-hill area (Lake Phewa) were studied for evaluating anthropogenic inputs of the pollutants, particularly mercury (Hg) and other trace elements (TEs) (such as Al, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb). A total of 77 water samples, 24 from Lake Gosainkunda and 53 from Lake Phewa were collected from different depth profiles during October/November 2010. Concentrations of Hg were significantly higher in Lake Gosainkunda compared to Lake Phewa probably due to long-range transport of Hg and its deposition on high altitudes of the Himalayas, in addition to the probable natural geological sources. Some of the TEs (such as Al, V, Cr, Mn, Fe, and Co) show crustal origin in Lake Gosainkunda, whereas others such as Ni, Cu, Zn, Cd, and Pb indicate possible anthropogenic origin (enrichment factor (EF) > 4). On the other hand, Al, V, Cr, Ni, and Cu show crustal origin in Lake Phewa and the remaining TEs (Mn, Fe, Co, Zn, Cd, and Pb) showed high EF values relative to the crustal elements suggesting potential anthropogenic inputs of the pollutants. The study further indicates that two studied lakes have different potential sources for Mn, Fe, Co, Ni, and Cu regarding TE pollution. A high enrichment of Cd and Pb in high-altitude lake (with less anthropogenic activities) compared to the low-altitude lake (with high anthropogenic activities) indicates atmospheric long-range transportation of the pollutants in remote areas of the Himalayas which might be possible as air masses pass through the industrial areas and deposit in the high altitudes.

A comprehensive chemical characterisation of the ionic and metallic composition of PM₂.₅fraction of suburban aerosol collected with high‐volume aerosol samplers at a coastal suburban site of northwest Atlantic European is studied over a 1.5-year period (from March 2011 to August 2012). The monthly mean PM₂.₅mass concentrations (after gravimetric measurement) ranged from 13 to 26 μg m⁻³. Eighteen samples, which provide information pertaining to the monthly variation in chemistry, were analyzed. Trace metals (Al, As, Ba, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sr, V and Zn) were analysed in PM₂.₅fraction after acid extraction (total metallic concentration) and after sonication-assisted water extraction (aqueous soluble fraction). Major inorganic ions (Cl⁻, NO₃⁻, SO₄²⁻, Na⁺, K⁺, Ca²⁺, Mg²⁺, NH₄⁺and C₂O₄²⁻) were also analysed in the aqueous fraction of PM₂.₅. Trace metal extractability in water was in the range 50–67 % with exception of Al (∼2 %), Fe (∼4 %) and Cr (∼18 %). After univariate, cluster (CA) and principal component (PCA) analyses and air mass backward trajectory analysis, marine, crustal and anthropogenic (including road traffic) sources were found for the inorganic composition of PM₂.₅. Results also suggest a great influence of cleaner Atlantic air masses and ubiquitous sources for K⁺, Mg²⁺, Fe, Ni and V.

2,3-Dihydroxybenzaldehyde modified silica gel (SGDHB) was prepared and then used for the removal of boron. Adsorption of boron on the SGDHB was examined with respect to the equilibrium adsorption, kinetics and as a function of pH. Boron is strongly retained on the SGDHB between pH 7 and pH 9. The results indicated that the adsorption equilibrium was well described by the Langmuir equation. The SGDHB exhibited an excellent sorption capacity with 3.812 mmol B/g SGDHB under experimental conditions. The material shows reasonably rapid sorption ability, with boron in 25 mL of 0.01 M H₃BO₃ solution being removed almost completely within 30 min of contact time with 0.12 g of the modified silica gel. The SGDHB was demonstrated to be an efficient sorbent for the removal of boron.

Nitrogen- heterocyclic polycyclic aromatic hydrocarbons (N-PAHs) are ubiquitous constituents of contaminated sites in which their high water solubility and lower k ₒw values imply greater mobility and impacts. Biodegradation is a major route of loss for organic contaminants in soil. In this study, microbial degradation was investigated in soil artificially contaminated with N-PAHs and monitored for over 200 days. The results showed that all the aromatic chemicals exhibited loss with increasing incubation time; however, only 0.05 ± 0.04 mg kg day⁻¹ loss was observed for N-PAHs at 10 mg kg⁻¹ amendments over the first 30 days incubation, with the exception of 4,7-phenanthroline which recorded 0.19 ± 0.03 mg kg day⁻¹. The study showed that soil microflora have the potential to degrade N-PAHs since all of the aromatics recorded chemical losses under aerobic condition. However, degradation rates varied between chemicals and this was attributed to N-atom position and/or number of N-substituents. Further, relatively little or no biodegradation was observed in B[h]Q amended soils with increasing concentration; indicating that B[h]Q is more resistance to biodegradation in soil.

Inactivation of pathogens present in animal manure prior to land application has justified the use of advanced technologies. However, some alternatives are expensive or not effective due to the organic material and suspended solids present in the effluent (e.g., ozone, UV light). The use of hydrated lime (calcium hydroxide, Ca(OH)₂) is an attractive wastewater treatment option due to the ability of lime to kill pathogens and to extract phosphorus from manure at an alkaline pH. The present study aimed to evaluate the soluble phosphorus removal and pathogen inactivation (Escherichia coli, Salmonella enterica serovar typhymurium and Porcine circovirus type 2), in the liquid fraction and in the solid generated after Ca(OH)₂ addition in swine wastewater, exposed for 3 and 24 h at different pH conditions: 9.0, 9.5, and 10.0. The results showed the efficiency of pH elevation with Ca(OH)₂ in the removal of soluble P at pH 9.0 and the total inactivation of E. coli, Salmonella, and P. circovirus type 2 at pH 10.0. The liquid fraction (reuse water) could be safely used for cleaning the swine production facilities, and the solid fraction (precipitated P) could be used as a secondary product and fertilizer.

High levels of marine salt deposition present in coastal areas have a relevant effect on road runoff characteristics. This study assesses this effect with the purpose of identifying the relationships between monitored water quality parameters and intrinsic site variables. To achieve this objective, an extensive monitoring program was conducted on a Portuguese coastal highway. The study included 30 rainfall events, in different weather, traffic, and salt deposition conditions. The evaluations of various water quality parameters were carried out in over 200 samples. In addition, the meteorological, hydrological, and traffic parameters were continuously measured. The salt deposition rates were determined by means of a wet candle device, which is an innovative feature of the monitoring program. The relation between road runoff pollutants and independent variables associated with weather, traffic, and salt deposition conditions was assessed. Significant correlations among pollutants were observed. A high salinity concentration and its influence on the road runoff were confirmed. Furthermore, the concentrations of the most relevant pollutants seemed to be very dependent on some meteorological variables, particularly the duration of the antecedent dry period prior to each rainfall event and the average wind speed.

In the present work, goethite (α-FeO(OH)) impregnated calcium alginate (Cal-Alg-Goe) beads were used to sorb the arsenic from groundwater without disturbing its physicochemical characteristics. Beads were formed by dropwise addition of homogenized mixer of goethite and 4 % sodium alginate solution in 0.2 M CaCl₂solution. Charge, size, and morphology of sorbents were characterized by using various techniques. The results of batch sorption experiments suggest that Cal-Alg-Goe beads are very effective for removal of arsenic in the pH range 3.0 to 7.5, and sorption was more than 95 % in the concentration range of 10–10,000 ng mL⁻¹. Beads were successfully tested for groundwater samples collected from areas having elevated levels of arsenic. Equilibrium sorption follows Langmuir isotherm model, and the maximum arsenic uptake calculated was 30.44 mg g⁻¹. The sorption kinetics could be explained by pseudo-first-order model, and the time needed for equilibrium was 24 h.

Cs is a common radionuclide present in nuclear wastes and released from nuclear power plant accidents. It is hard to be removed from water with traditional technology. The current study aimed at developing of efficient cost-effective adsorbent for removing Cs with modified MCM-41 with specific functional groups –SH. Mesoporous material MCM-41 was selected due to its large surface area and tunable pore structure. Functional –SH groups were grafted into the pores of MCM-41 to enhance its capability of selective adsorption of Cs from multi-element (Co, Sr) water solution. The adsorption results showed that the maximum adsorption capacity was 29.24 mg/g. Both Langmuir and Freundlich models described the adsorption processes of Cs, indicating co-existence of both monolayer and multilayer adsorption in the surface and inner pores of the materials. TEM, FTIR, and Raman spectroscopy analyses indicated that –SH groups were successfully bounded into the pores of MCM-41. The present study approved the surface functional modified MCM-41 which might be a good alternative candidate for cleaning up of radionuclide Cs from nuclear power plant accidents and relevant nuclear accident events.

The aim of the study was to estimate the influence of soil pH on the uptake of copper, zinc, and manganese by Valeriana officinalis. Preliminary studies involved soil analyses to determine acidity, organic matter content, and copper, zinc, and manganese total and bioavailable forms. The study involved atomic absorption spectrometry to determine the concentration of the elements, and mineral soil of pH = 5.1 was used in the study, as being typical for central Poland. The copper, zinc, and manganese contents were determined in plants grown in soils which had been modified to cover a wide range of pH values 3÷13. The intensity of germination was strongly pH dependent with the highest yield obtained in original, unmodified soil. Surprisingly, high soil alkalinity stimulated copper and manganese uptake while at the same time resulting in a decrease in zinc content.