Malathion is an organophosphate insecticide registered for use in cities throughout North America to control adult mosquitoes. The objective of this study was to determine the impact of urban malathion applications on the levels of malathion detected in bulk deposition. In 2010, malathion was applied by the City of Winnipeg’s Insect Control Branch for a total amount of 6632 kg in the city, as well as by the general public in relatively small amounts. In 2011, no malathion was applied by the city. Malathion was detected in 41 % of the samples in 2010 with deposition rates ranging from 0.5 to 107.7 μg/m²/week. Only 9 % of the samples contained malathion in 2011 with deposition rates always being <0.4 μg/m²/week. Between 6 and 25 % of the samples in 2010 exceeded the toxicological threshold levels of malathion to a range of freshwater amphipods, water fleas, and stoneflies, including Daphnia magna which is a bioindicator of good environmental health. The weekly maximum malathion concentration detected in this study (5.2 μg/L for a week in June 2010) was at least 26 times greater than the maximum concentration of malathion reported in other atmospheric deposition studies. For the two insect management areas (7.4 and 37.6 km²) where the bulk deposition samplers had been placed, calculations suggested that between 1.2 and 5.1 % of the malathion applied by the city became bulk deposition. Percutaneous absorption by humans of malathion in rainfall is unknown.

The internal concentration represented by the critical body residue (CBR) is an ideal indicator to reflect the intrinsic toxicity of a chemical. Whilst some studies have been performed on CBR, the effect of exposure route on internal toxicity has not been investigated for fish. In this paper, acute toxicity data to fish comprising LC₅₀ and LD₅₀ values were used to investigate CBR. The results showed that exposure route can significantly affect the internal concentration. LD₅₀ and CBR calculated from LC₅₀ and BCF both vary independently of hydrophobicity as expressed by log Kₒw; conversely, LC₅₀ is related to log Kₒw. A poor relationship was observed between LC₅₀ and LD₅₀, but the relationship can be improved significantly by introduction of log Kₒw because log CBR is positively related to log LD₅₀. The parallel relationship of log CBR-log Kₒw and log LD₅₀-log Kₒw indicates that LD₅₀ does not reflect the actual internal concentration. The average LD₅₀ is close to the average CBR for less inert and reactive compounds, but greater than the average CBR for baseline compounds. This difference is due to the lipid fraction being the major storage site for most of the baseline compounds. Investigation on the calculated and observed CBRs shows that calculated CBRs are close to observed CBRs for most of compounds. However, systemic deviations of calculated CBRs have been observed for some compounds. The reasons for these systemic deviations may be attributed to BCF, equilibrium time and experimental error of LC₅₀. These factors are important and should be considered in the calculation of CBRs.

The paper presents the results of antimony removal from the Dúbrava water resource using a pilot plant system capable of taking samples from different heights of adsorption materials. The adsorbents GEH, CFH12, CFH18, and Bayoxide E33 and two experimental stainless columns with bleeder valves located at heights of 20, 45, and 70 cm of the adsorption media and 91 cm (GEH), 94 cm (CFH18), 87 cm (CFH12), and 87 cm (Bayoxide E33) filter media high were used. The results of the experiments show that the most suitable material for removing antimony from water is GEH. For an antimony concentration of 78.4–108.0 μg/L in raw water and a filtration rate of 5.6–5.9 m/h, the limit concentration of 5 μg/L at the outlet of the 70-cm high adsorption media was reached at the bed volume 1788. In a case when the media height was 91 cm, the antimony concentration in the treated water would reach the limit value of 5 μg/L after a 672-h operation of the stainless column at the bed volume 4256. Under these conditions, the adsorption capacity was calculated at 184 μg/g. The adsorption capacities and bed volumes of the other adsorbents were lower in comparison to GEH.

This paper proposes an extraction procedure for the speciation analysis of inorganic antimony in sediment samples using slurry sampling and hydride generation atomic absorption spectrometry. The optimization step of extraction of the species was performed employing a full two-level factorial design (2³) and a Box-Behnken matrix where the studied factors in both experiments were: extraction temperature, ultrasonic radiation time, and hydrochloric acid concentration. Using the optimized conditions, antimony species can be extracted in closed system using a 6.0 M hydrochloric acid solution at temperature of 70 °C and an ultrasonic radiation time of 20 min. The determination of antimony is performed in presence of 2.0 M hydrochloric acid solution using HG AAS by external calibration technique with limits of detection and quantification of 5.6 and 19.0 ng L⁻¹ and a precision expressed as relative standard deviation of 5.6 % for an antimony solution with concentration of 6.0 μg L⁻¹. The accuracy of the method was confirmed by analysis of two certified reference materials of sediments. For a sample mass of sediment of 0.20 g, the limits of detection and quantification obtained were 0.70 and 2.34 ng g⁻¹, respectively. During speciation analysis, antimony(III) is determined in presence of citrate, while total antimony is quantified after reduction of antimony(V) to antimony(III) using potassium iodide and ascorbic acid. The method was applied for analysis of six sediment samples collected in São Paulo Estuary (Bahia State, Brazil). The antimony contents obtained varied from 45.3 to 89.1 ng g⁻¹ for total antimony and of 17.7 to 31.4 ng g⁻¹ for antimony(III). These values are agreeing with other data reported by the literature for this element in uncontaminated sediment samples.

This study examined a single underground coal mine and investigated two aspects of its operation: the disposal of the mine waste through a discharge to a nearby river and the impact of subsidence from an underground longwall to a small waterway above. Water quality of the two waterways was monitored over a 2-year period with a monthly investigation over a 6-month period, which included collection of stream macroinvertebrates. Both mine activities modified surface water geochemistry and macroinvertebrate communities. Mean electrical conductivity (EC) increased in surface waters below the mine discharge, rising 4.8 times from (186 μS/cm) upstream to 1078 μS/cm below the waste inflow. Mean EC increased in a small stream that was disturbed by subsidence from longwall mining, rising 3.8 times from (247 μS/cm) upstream to 1195 μS/cm below. The mineral constituents of the increased salinities were different. The coal mine wastewater discharge was enriched with sodium and bicarbonate ions compared to sodium and chloride ions in the subsidence affected creek. Both the waste discharge and the subsidence caused increases in the concentrations of zinc by about four times and nickel by 20 to 30 times the background levels. The subsidence reduced dissolved oxygen to ecologically stressful levels and increased iron and manganese concentrations by about 20 times the background levels. Two of the key changes in stream ecosystems were a reduction in the proportion of mayfly larvae downstream of the mine waste discharge and mosquito larvae dominating (60–70 % of total abundance) the invertebrate community in the subsidence affected creek.

The potential of agricultural waste materials for the removal bisphenol A (BPA) from aqueous solution was investigated. BPA is an endocrine-disrupting compound (EDC) used mainly in the plastic manufacturing industry. It may be hazardous to humans and animals because of its estrogenic activity. Agricultural wastes are sustainable adsorbents because of their low cost and availability. Hence, this study investigated the removal of BPA from water by adsorption onto treated coir pith, coconut shell and durian peel. The adsorption of BPA from water onto adsorbent was evaluated using field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET). The effects of morphology, functional groups, and surface area on adsorption before and after pretreatment with sulfuric acid and reaction were investigated, and it was found that the treated adsorbent were able to remove BPA. Carbonyl and hydroxyl groups had appear in large number in FTIR analysis. The present study indicates that coir pith had removed 72 % of BPA with adsorption capacity of 4.308 mg/g for 24 h, followed by durian peel (70 %, 4.178 mg/g) and coconut shell (69 %, 4.159 mg/g). The results proved that these modified phyto-waste were promising materials as alternative adsorbent for the removal of BPA from aqueous solution.

Nikola Tesla B power plant (TENT-B), located on the Sava River in Obrenovac, 52 km west from the Serbian’s capital, Belgrade, is the second largest coal-fired power plant in the country, consisting of two blocks of 620 MW each. Samples of fresh coal ash obtained by coal combustion in TENT-B, as well as coal ash samples from the surface and 1-m depth of active, currently filled, and passive, previously filled and not currently used, cassettes, were taken from the coal ash dump. Ultrasonic extracts of the samples were analyzed using gas chromatography with mass selective detection (GC/MSD) in order to identify and quantify 16 priority polycyclic aromatic hydrocarbons (PAHs). Two PAH extraction mechanisms during coal ash dumping and storage processes are discussed and significant differences between them were established. PAH concentrations in the ash samples were compared statistically. Correlations between samples and sampling points were established, and leaching potential of samples was examined. Concentrations of PAHs can be reduced in coal ash sediments by environmental influences only after long time periods, and PAHs with two six-membered rings pose danger to underground waters, while PAHs with three rings pose danger to soil sediments.

Grass from municipal roadside verges is a potential yet largely unused resource for bioenergy recovery, which is mainly due to its unknown elemental composition. Therefore, we measured the concentration of 16 elements (Ca, K, Mg, N, Na, P, S, Al, Cd, Cl, Cr, Cu, Mn, Pb, Si and Zn) in a material from the city of Kassel harvested in different management intensities. The element concentrations were mainly close to reference values of agricultural or nature conservation grassland and usually within the range of literature data. Concentrations of most elements, including heavy metals, were below limiting values. Only N and Cl concentrations in the raw material exceeded the limiting values for combustion, but washing and dewatering of the biomass with the “integrated generation of solid fuel and biogas from biomass” technique resulted in concentrations in the press cake well below the limiting values. Considering the element concentrations of grass from urban roadside verges, utilisation for energy recovery may be possible, provided an appropriate technology is applied.

Biochar is an organic carbon (OC) and plant nutrient-rich substance that may be an ideal amendment for bolstering soil organic matter and nutrient contents. Two biochars were produced by pyrolysis at 350 °C from pine chips (Pinus taeda) and swine manure solids (Sus scrofa domesticus). The biochar total elemental composition was quantified using inductively coupled plasma spectrometer and their surface chemical composition examined using a combination of scanning electron microscopy (SEM) and electron dispersive spectroscopy (EDS). The biochars were mixed into triplicate pots containing Lauderhill muck (Euic, hyperthermic Lithic Haplosaprist) at 0, 2.5, 5, and 10 % (dry mass). Four simulated water infiltration events were conducted during the 124-day incubation to assess the potential alteration in the leaching potential of soluble soil nutrients. At termination, the muck’s fertility characteristics were assessed, and dissolved cations were measured in water leachates. Neither biochars significantly increased the muck’s OC contents. Swine manure biochar contained higher K, Mg, Na, and P concentrations, and these differences were observable in SEM and EDS as differing amounts of surface-precipitated Mg and K salts. Correspondingly, swine manure biochar at all three applications rates significantly increased Mehlich 1-s K, P, Mg, and Na concentrations. Pine chip biochar only improved the Mehlich 1-extractable K concentration but did reduce soluble P concentrations. Water leachates from swine manure biochar treated wetland soil contained significantly higher soluble P concentrations that could create water quality issue in downstream ecosystems.