Accumulation of metals in aquatic organisms is influenced by several factors, including the presence of other metals; therefore, there is a need to study the effects of mixtures of other metals on the accumulation of a particular metal on the organisms. In this study, the capacity for nickel (Ni) regulation by the juvenile decapod crustacean Penaeus vannamei was analyzed. The effects of both solely Ni exposure and in the presence of other metals such as zinc (Zn), lead (Pb), and cadmium (Cd) in a mixture were analyzed to determine any possible synergism. A previous study revealed that a metal mixture of Zn, Cd, and Pb without Ni induces a higher metal uptake in P. vannamei for all three metals, but in this study, no effect was observed for Ni. The results showed no change in the regulatory capacitance for Ni, even in the presence of other metals. The observed capacity of P. vannamei to regulate body concentrations of nickel prevents its use as a suitable biomonitor for this metal.

In this study, the effectiveness of subcritical water extraction (SCWE) was assessed by extracting four pesticides, namely diazinon, parathion, phenthoat, and EPN, from contaminated soil. The extraction efficiencies of different temperatures (25, 75, 100, 125, and 150 C); times (10, 20, 30, and 40 min); pressures (1, 2, and 3 MPa); and water flow rates (0.5, 0.7, 1.0, and 1.5 mL/min) were investigated. The optimum temperature, time, pressure, and flow rate were found to be 150 C, 20 min, 2 MPa, and 0.5 mL/min, respectively, in lab-scale. At this operating condition, the residual concentration of pesticide was less than 0.5 mg/kg, corresponding to an extraction efficiency of 99.9 %. The aim of this study was to also evaluate the removal efficiency on 30- and 167-fold scale-up extraction at optimum extraction condition obtained from lab-scale studies. The scale-up method considering constant ratio of the volume of water to soil mass was a feasible procedure. The results of our study suggest that SCWE is a promising option for effective disposal of pesticide- contaminated soil. © 2013 Springer Science+Business Media Dordrecht.

A better understanding of the effect of anthropogenic pollution on the formation of toxic Microcystis blooms is particularly important in regions with large urban centres where rivers, lakes, and estuaries receive large quantities of contaminated domestic and industrial wastes. The response of the bloom-forming cyanobacteria Microcystis aeruginosa CALU 972 and CALU 973 from Russian Karelia to pollution was investigated. The contaminants caused compensatory-adaptive changes that led to the retention of cell viability in the cyanobacterial cells. The adaptation to metals and 1,2,4-triazole was realised due to photosystem changes and the enhanced production of organic compounds, such as proteins and exopolysaccharides. Nutrients caused a significant increase in biomass production by M. aeruginosa. The exposure of M. aeruginosa to nutrients and zinc stimulated growth and contributed to enhanced microcystin concentrations. Variants of microcystins responded differently to pollution. Contaminants had pronounced effects on microcystin RR levels but less effects on microcystin LR levels. Heavy metals, 1,2,4-triazole and nitrogen influenced microcystin concentrations by affecting both the growth of Microcystis and hepatotoxin release into the environment.

The objectives of this study were to assess susceptibility to acidification and nitrogen (N) saturation caused by atmospheric deposition to northeastern US forests, evaluate the benefits and shortcomings of making critical load assessments using regional data, and assess the relationship between expected risk (exceedance) and forest health. We calculated the critical loads of nutrient N and of sulfur (S) + N using the steady-state mass balance method at >4,000 regional and national vegetation and soil monitoring network plots in the northeastern USA. Regional calculations of critical loads necessitate use of soil maps which provide a range for each soil characteristic resulting in a broad range of critical load of S + N and exceedance values. For the scenario most representative of regional conditions, over 80 % of the critical loads fell into the range of 850–2050 eq ha⁻¹ yr⁻¹; at 45 % of the plots, deposition exceeded the critical load. In contrast, the critical load for nutrient N, 200–300 eq ha⁻¹ yr⁻¹, was lower. Site measurements, especially to estimate soil weathering, would increase the certainty of the critical load. We observed significant negative correlations between critical load exceedance and growth (17 species) and crown density (4 species); we observed significant positive correlations of exceedance with declining vigor (four species), with crown dieback (six species) and crown transparency (seven species). Among the species which demonstrate the most significant detrimental responses to atmospheric deposition are balsam fir, red spruce, quaking aspen, and paper birch. These results indicate that significant detrimental responses to atmospheric deposition are being observed across the northeastern USA.

Pyrite, FeS₂, is the most common sulfide mineral. The aim of this work was to assess the oxidative ability of H₂O₂ in presence of natural pyrite by employing reactive black 5, acid red GR, and cationic red X-GRL as model pollutants. The effects of H₂O₂ dosage, pyrite loading, and initial pH on reaction were investigated. The results reveal that natural pyrite-promoted H₂O₂ has a great activity in the decoloration of azo dyes. About 85 % of reactive black 5 and acid red GR can be removed within 10 min when 0.3 mM H₂O₂ and 0.3 g/L pyrite are used with initial pH values ranging from 6.32 to 6.96. The discoloration efficiencies are demonstrated to be less sensitive to the initial solution pH value. Approximately 90 % of discoloration for reactive black 5 and acid red GR can be achieved when initial pH value ranges from 2 to 10. Ion leaching experiments show that high levels of ferrous iron and sulfate can be detected when natural pyrite is added to dye solution alone. To gain an understanding of the reaction mechanism and the role of natural pyrite takes in these processes, techniques including scanning electron microscope, X-ray diffraction, and X-ray photoelectron were employed to characterize the solid sample and ion leaching experiments were also carried out. Results indicate that the determined high levels of ions have resulted from the dissolution of FeSO₄·H₂O formed on the surface of pyrite and the homogeneous Fenton reaction initiated by ferrous iron in presence of H₂O₂ is mainly responsible for the observed fast color removal rate.

The sorption of chromium (Cr) species to soil has become the focus of research as it dictates the bioavailability and also the magnitude of toxicity of Cr. The sorption of two environmentally important Cr species [Cr(III) and Cr(VI)] was examined using batch sorption, and the data were fitted to Langmuir and Freundlich adsorption isotherms. The effects of soil properties such as pH, CEC, organic matter (OM), clay, water-extractable SO₄ ²– and PO₄ ³–, surface charge, and different iron (Fe) fractions of 12 different Australian representative soils on the sorption, and mobility of Cr(III) and Cr(VI) were examined. The amount of sorption as shown by K f was higher for Cr(III) than Cr(VI) in all tested soils. Further, the amount of Cr(III) sorbed increased with an increase in pH, CEC, clay, and OM of soils. Conversely, the chemical properties of soil such as positive charge and Fe (crystalline) had a noticeable influence on the sorption of Cr(VI). Desorption of Cr(VI) occurred rapidly and was greater than desorption of Cr(III) in soils. The mobility of Cr species as estimated by the retardation factor was higher for Cr(VI) than for Cr(III) in all tested soils. These results concurred with the results from leaching experiments which showed higher leaching of Cr(VI) than Cr(III) in both acidic and alkaline soils indicating the higher mobility of Cr(VI) in a wide range of soils. This study demonstrated that Cr(VI) is more mobile and will be bioavailable in soils regardless of soil properties and if not remediated may eventually pose a severe threat to biota.

To clarify the relationship between the transport distance of spheroidal carbonaceous particles (SCPs) and particle size, we investigated the spatial distribution of SCP sizes in swimming pool deposits in the central Osaka Plain, central Japan. Median particle size of SCPs generally decreases with distance (0 to ∼20 km) downwind from the local coastal industrial area where SCP sources are distributed widely. This suggests that most SCPs found in the study area are derived from the industrial area. Samples with >40 % of particles >20 μm were predominantly collected within 2 km of the industrial area, while samples with >40 % of particles <10 μm were mostly collected over 10 km from the industrial area. Based on the results of our study and previous studies, we conclude that a higher proportion of particles of size >20 μm indicates that the origin of SCPs is within a few kilometres upwind of the sample site, whereas the presence of higher proportion of particles <10 μm indicates that their source is generally further than 10 km upwind. However, other factors may affect the size distribution of SCPs at a given location (e.g. fuel type, quality of the particle precipitator and topography of the terrain). Pool deposits provide more suitable samples than lake sediments for investigating atmospheric precipitation.

The successive alkalinity-producing passive system (SAPPS) located in Gangneung, South Korea was designed to treat acid mine drainage. The performance of SAPPS has been monitored intensively for 3 years at the component level (influent, settling pond A, the successive alkalinity-producing system (SAPS), settling pond B, constructed wetland, and effluent). This study evaluated the ability of SAPPS to remove acidity and iron from influents at flow rates ranging from 17 to 160 m3/day. The concentration of soluble Fe total was the highest, and the pH was the lowest at low flow rates (≤61 m3/day). When flow rates were over 80 m3/day, concentrations decreased and Fetotal was removed primarily at the SAPS stage. For flow rates of less than 61 m3/day, Fetotal was removed at the SAPS stage as well as in settling pond B and at the constructed wetland. Hydraulic retention times of 1 and 2 days were found to be appropriate and economical for use with the SAPS stage and for settling pond B and the constructed wetland, respectively The treatment of acid mine drainage by conventional SAPPSs is limited by the availability of alkaline materials. However, the new proposed system can address this weakness through the provisioning of a suitable alkalinity supply. © 2013 Springer Science+Business Media Dordrecht.

Analytical measurements are commonly used to screen for toxicity or lack of toxicity from sediment-associated copper. Comparisons of analytical measurements with toxicological responses can be useful for determining the practicality of analytical measurements for assessing the toxicity of copper in sediments. The purpose of this research was to determine the utility of method detection limits (MDLs; i.e., minimum concentration of an analyte such as copper that can be measured with 99 % confidence with a specific analytical method and matrix) to predict the bioavailability of copper in five different sediments. The specific objectives of this research were to (1) select and characterize five sediments with different characteristics, (2) amend and measure a range of copper concentrations in the five sediments to determine MDLs and bioavailability of copper amendments in those sediments, (3) discern relationships with sediment characteristics to MDLs and bioavailability of copper in the five sediments, and (4) compare MDLs and observed toxicity to Hyalella azteca Saussure as an indicator of copper bioavailability in the five sediments. The lowest copper concentrations that elicited an observable adverse effect ranged from 15 to 550 mg Cu/kg, and the MDLs ranged from 1.5 to 6 mg Cu/kg. The MDLs and measured copper concentrations were not adequately predictive of the bioavailability and toxicity of copper in the five sediments. No adverse effects were observed for H. azteca exposed for 10 days to the sediment from California with simultaneously extractable metals > acid-volatile sulfides. Since the lowest observed effects concentrations of copper in the five sediments ranged two orders of magnitude, the National Oceanic and Atmospheric Administration screening values (threshold and probable effect levels) were not predictive of H. azteca responses to the copper-amended sediments.

Bisphenol-A (BPA) is an environmental contaminant used in the manufacturing of polycarbonate plastics and epoxy resins, which has been discovered in freshwater systemsworldwide as a result of effluent from manufacturing. This bioactive molecule is an estrogen mimic and has become a concern for exposure, especially during development, resulting in its removal from baby bottles and other consumer products. BPA is an endocrine disruptor in a variety of species and has been classified as a toxic substance in multiple countries. In this study, we examined the effect of BPA exposure on leukocyte counts in wild yellow perch, Perca flavescens. Yellow perch were exposed to either 2, 4, and 8 ppb BPA; Saprolegnia; or a blank control for a period of 7 days. Leukocyte blood counts were significantly higher in Saprolegnia, 4 ppb BPA, and 8 ppb BPA treatments compared to control. To test compound effects of BPA and Saprolegnia on leukocyte counts over a 7-day period, perch were exposed to either 4 ppb BPA, 4 ppb BPA+Saprolegnia, or control. Leukocyte counts were significantly higher in the 4 ppb BPA treatment relative to control. The 4 ppb BPA+Saprolegnia treatment was numerically elevated from the control, exhibiting a 153 % increase relative to control. BPA represents a contaminant with immunomodulatory properties that remain to be determined. © Springer Science+Business Media Dordrecht 2013.