Although many studies have examined effects of metal mine effluents (MMEs) on receiving environments, few have compared the roles of individual and mixed metals relative to whole effluents. The objective of the present set of studies was to examine whether Cu, Ni, or Se, alone or in a mixture, causes comparable effects to those observed in fathead minnows (Pimephales promelas) exposed to an environmentally relevant MME (45 % process water effluent [PWE]). Metal bioaccumulation, fathead minnow (FHM) morphometrics, and egg production were compared between treatments over a 21-day exposure. FHMs were exposed to similar waterborne concentrations and species of metals in single and mixed metal treatments relative to 45 % PWE. FHMs were also exposed to similar concentrations of metals in single and mixed metal treatments relative to 45 % PWE through the diet (Chironomus dilutus — a representative prey species). However, only FHMs exposed to 45 % PWE had reduced egg production (60–80 % less than controls). Our findings indicate that Cu, Ni, and Se exposures and bioaccumulation did not contribute to decreased reproductive output in FHMs under the conditions that were examined. We also found no evidence to believe that these metals were responsible for decreased egg production in PWE. It is therefore reasonable to suggest that these metals have limited potential to cause reproductive effects in MMEs with similar composition and water chemistry conditions. Overall, this study highlights the importance of examining single and mixed metal exposures prior to suggesting that adverse effects in fish exposed to MMEs occur due to bioaccumulation of metal(s).

Total atmospheric bulk mercury (Hg) concentration and deposition were measured from August 2008 to November 2010 at nine locations in the Northern Great Plains, USA using passive bulk mercury samplers. Monthly mercury concentrations ranged from 1.3 to 51.0 ng L⁻¹ with an overall volume weighted mean of 12.9 ng L⁻¹. Normalized daily Hg fluxes ranged from 0.43 to 110 ng m⁻² day⁻¹ with higher rates occurring during high precipitation months as rainfall during spring and summer. Annual deposition rates ranged from 5.82 to 9.21 μg m⁻² year⁻¹ and were comparable to studies performed at similar latitudes and to estimates from the Mercury Deposition Network (MDN). There was no significant difference (p > 0.05) between measured atmospheric mercury for one colocated bulk Hg sampler and an existing MDN wet-only sampler at Eagle Butte, South Dakota, demonstrating measurement unity between the two sampling techniques in this geographic area.

The development of human society entails increased industrial activity and consequently the release of a large number of chemical substances including solvents, detergents and pharmaceutical products which reach water bodies through the discharge of industrial effluents, damaging the organisms living in these ecosystems. This study aimed to determine oxidative stress induced on the common carp Cyprinus carpio by effluent from a pharmaceutical plant that manufactures nonsteroidal anti-inflammatory drugs. The median lethal concentration and subsequently the lowest observed adverse effect level were determined. Carp were exposed to the latter value (0.1173 %) for different exposure periods (12, 24, 48, 72 and 96 h), and the following biomarkers were evaluated in gill, brain, liver and blood: hydroperoxide content (HPC), lipid peroxidation (LPX), protein carbonyl content (PCC), and the activity of the antioxidant enzymes superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx). Statistically significant increases with respect to the control group (P < 0.05) were observed in HPC, LPX and PCC particularly in gill of effluent-exposed specimens. SOD, CAT and GPx activity in gill also increased with respect to the control group. This particular industrial effluent is therefore concluded to induce oxidative stress on C. carpio, this damage being most evident in gill. © 2013 Springer Science+Business Media Dordrecht.

Two methods to measure mercury concentration in soil are compared, and their compliance with international standards is determined: cold vapour atomic absorption spectrometry and thermal decomposition, amalgamation and atomic absorption spectrophotometry. The detection limit, quantification limit and uncertainty of these two analytical methods were evaluated and compared. The results indicated that thermal decomposition, amalgamation and atomic absorption spectrophotometry had a lower quantification limit and uncertainty than cold vapour atomic absorption spectrometry (quantification limit, 0.27 vs. 0.63 mg kg⁻¹; expanded uncertainty, 9.30 % vs. 10.8 %, respectively). Thermal decomposition, amalgamation and atomic absorption spectrophotometry allowed the determination of the base values for the concentration of mercury in soil recommended by international standards, achieving a lower detection limit than cold vapour atomic absorption spectrometry under the study conditions. In addition, thermal decomposition, amalgamation and atomic absorption spectrophotometry represent a more environmentally friendly alternative for mercury determination because this method uses fewer reagents and therefore generates less waste.

In this study, arsenate removal by apricot stone-based activated carbon (IAC) modified with iron (oxy-hydr)oxides was carried out. For this purpose, hybrid adsorbents based on Fe²⁺-loaded activated carbon (IAC–Fe(II)) and Fe³⁺-loaded activated carbon (IAC–Fe(III)) were synthesized by precipitation method. A three-level, three-factor Box–Behnken experimental design combined with response surface methodology (RSM) was employed to find the optimum combination of process parameters for maximizing the As(V) adsorption capacity of activated carbon-based iron-containing hybrid adsorbent. Three important operation parameters, namely, initial pH of solution (3.0–7.0), temperature (25–65 °C), and initial As(V) concentration (0.5–8.5 mg L⁻¹), were chosen as the independent variables, while the As(V) adsorption capacities of hybrid adsorbents were designated as dependent variables. Lack of fit test showed that the quadratic model provided the best fit to experimental data for both adsorbents with the highest coefficients of determination (R ²), adjusted R ², and p-values for lack of fit. The standardized effects of the independent variables and their interactions were tested by analysis of variance and Pareto chart. The model F-values (F IAC–Fₑ₍II₎=330.39 and F IAC–Fₑ₍III₎=36.19) and R ² values (R ² IAC–Fₑ₍II₎=0.9977 and R ² IAC–Fₑ₍III₎=0.9789) of second-order polynomial regression equations indicated the significance of the regression models. Optimum process conditions for As(V) adsorption onto IAC–Fe(II) were 63.68 °C, pH 3.10, and 8.4 mg L⁻¹ initial arsenic concentration, while 25.22 °C, pH 3.07, and 8.28 mg L⁻¹ initial As(V) concentration were found to be optimum conditions for IAC–Fe(III).

Arsenic (As) toxicity and the effects of nitric oxide (NO), supplied as sodium nitroprusside (SNP), were analyzed in Pistia stratiotes. The plants, which were grown in nutrient solution at pH 6.5, were exposed to four treatments for 24 h: control; SNP (0.1 mg L-1); As (1.5 mg L-1); and As + SNP (1.5 and 0.1 mg L-1). As accumulated primarily in the roots, indicating the low translocation factor of P. stratiotes. The As accumulation triggered a series of changes with increasing production of reactive oxygen intermediates and damage to cell membranes. The application of SNP was able to mitigate the harmful effects of As. This attenuation was probably due to the action of the SNP as an antioxidant, reducing the superoxide anion concentration, and as a signaling agent. Acting as a signal transducer, SNP increased the activity of enzymatic antioxidants (POX, CAT, and APX) in the leaves and stimulated the entire phytochelatins biosynthetic pathway in the roots (increased sulfate uptake and synthesis of amino acids, non-proteinthiols, and phytochelatins). The As also stimulated the phytochelatins biosynthesis, but this effect was limited, probably because plants exposed only to pollutant showed small increments in the sulfate uptake. Thus, NO also may be involved in gene regulation of sulfate carriers. © 2013 Springer Science+Business Media Dordrecht.

Oxidative degradation of ethylenediaminetetraacetic acid (EDTA) in aqueous solution at normal temperature and pressure by the bimetallic Fe–Cu was investigated in this work. The results showed that the removal efficiency of EDTA, total organic carbon (TOC), and total nitrogen (TN) could be about 95, 62.5, and 39 %, respectively, after 3-h reaction. The degradation of EDTA followed the pseudo-first-order reaction kinetics and would not be affected by the continuous use of bimetallic Fe–Cu. The degradation products were iminodiacetate, formate, and acetate determined by ion chromatogram. The effects of initial pH, initial concentration of EDTA, Cu content, Fe–Cu loading, and atmosphere were also investigated. Significantly, the bimetallic Fe–Cu process exhibited higher reactivity than ZEA process for the degradation of EDTA and it would not cause new heavy metal pollution in effluent. Reactive oxygen species (ROS) of OH was generated in situ. The evidence of oxidative degradation of EDTA was verified by electron spin resonance (ESR) spectroscopy and the product of para-hydroxybenzoic acid (p-HBA) by OH and benzoic acid (BA).

The purpose of this study was to determine the effect of soil contamination with tri- and hexavalent chromium and soil application of compost, zeolite, and CaO on the mass of oats and content of nitrogen compounds in different organs of oats. The oats mass and content of nitrogen compounds in the crop depended on the type and dose of chromium and alleviating substances incorporated to soil. In the series without neutralizing substances, Cr(VI), unlike Cr(III), had a negative effect on the growth and development of oats. The highest doses of Cr(VI) and Cr(III) stimulated the accumulation of total nitrogen but depressed the content of N-NO₃ ⁻ in most of organs of oats. Among the substances added to soil in order to alleviate the negative impact of Cr (VI) on the mass of plants, compost had a particularly beneficial effect on the growth and development of oats. The application of compost, zeolite, and CaO to soil had a stronger effect on the content of nitrogen compounds in grain and straw than in roots. Soil enrichment with either of the above substances usually raised the content of nitrogen compounds in oats grain and straw, but decreased it in roots.

Knowledge of the levels of both total metal content and metal bioavailability is critical for understanding the long-term effects of liming on soil chemistry and potential metal uptake by biota. In the present study, the long-term effects of liming on metal bioavailability in soils contaminated by smelter emissions were assessed in eroded and stable uplands in the Sudbury region, Ontario, Canada. Analytical results revealed that total metal and nutrient contents of the soil matrix are not dominantly in forms available for plant uptake for these soils. On average, only 1 and 1.1 % of total copper and nickel, respectively, were phytoavailable. Landscape topography, site stability, and smelter proximity all play an important role in metal accumulation in the surface organic and mineral horizons of regional soils. The levels of total and bioavailable elements for eroded sites were always smaller for stable and reference sites. The pH in limed sites was significantly higher, ranging from 4.12 to 6.75, in the humus form compared to unlimed areas, even 20 to 30 years following applications of the crushed dolostone (liming). No significant differences between limed and unlimed areas were found for total metal and nutrient contents. Interestingly, in the higher pH limed areas, the levels of bioavailable Al, Co, Cu, Fe, K, Mn, Ni, and Sr were lower than on unlimed areas. © 2013 Springer Science+Business Media Dordrecht.

Wild birds have been shown to be significant sources of numerous types of pathogens that are relevant to humans and agriculture. The presence of large numbers of migratory birds in such a sensitive and important ecosystem as the Platte River in central Nebraska, USA, could potentially serve a significant source of bird-derived pathogens in the water/sediment and riverine environment. In 2009 and 2010, a study was completed to investigate the potential water-quality impacts of Sandhill Cranes and Snow Geese on the microbial water quality of the central Platte River during their spring migration period. Fecal material, river-bottom sediment, and water samples were collected from January through May of each year during the spring migration season of Sandhill Cranes in the Central Flyway of North America. Results indicate that several types of fecal indicator bacteria and from a range of viral, protozoan, and bacterial pathogens, Campylobacter jejuni were present in Sandhill Crane excreta, and at significantly higher frequency and densities in water and sediments when the Sandhill Cranes were present, particularly during evening roosts within the Platte River environment. Therefore, further investigation of the health significance of avian pathogens is warranted for the Platte River in Central Nebraska during migration of Sandhill Cranes and other waterfowl.