This article evaluates various extraction techniques’ suitability for soil mercury phytoavailable fraction assessment, including DGT method and extraction with microscopic filamentous fungi metabolites, MgCl₂, rainwater, and EDTA. After mercury extraction from contaminated soils by these techniques, the obtained data were compared to mercury accumulation by shoots of barley (Hordeum vulgare L.). Comparison of these values showed that DGT method is able to separate soil mercury with the best agreement to total mercury concentration in shoots of barley. However, comparing mercury extraction efficiency of selected techniques to extraction efficiency of barley, statistical significance at 0.05 significance level was proved for fungal Cladosporium sp. and Alternaria alternata metabolites. Our results indicate that these extraction techniques are suitable for risk assessment of mercury phytoavailability in contaminated areas.

The electrokinetic transport of sulfate was investigated as a means of treating and restoring a sulfate-accumulating saline soil. The electrokinetic treatment decreased the electrical conductivity of the soil, an indicator of soil salinity, to 58.6, 73.1, and 83.5 % for 7, 14, and 21 days, respectively. More than 96 % of the chloride and nitrate were removed within 7 days. However, the removal of sulfate was highly influenced by the anode material. An iron anode removed sulfate effectively, whereas sulfate was hyper-accumulated in the anodic region when an inert anode was used. The iron anode was oxidized in a sacrificial anodic reaction, which competed with the electrolysis reaction of water at the anode, and finally, the reaction prevented the severe acidification of the soil in the anodic region. However, the competing reactions produced hydrogen ions at the anode and the ions were transported toward the cathode, which, in turn, acidified the soil, especially in the anodic region. The acidification switched the surface charge of the soil from negative to positive, increasing the interaction between the soil surface and sulfate and thus inhibiting the transport of sulfate under the electric field. The zeta potential analysis of the soil provided an explanation. The results indicate that preventing severe acidification is an important factor which influences the transport of anions and iron anode for the enhanced removal of anionic pollutants by electrokinetic remediation.

Phytoremediation has been proven to be an environmentally sound alternative for the recovery of contaminated soils, and the economic profit that comes along with the process might stimulate its field use. This study investigated cadmium (Cd) transfer and detoxification mechanisms in a soil–mulberry–silkworm system to estimate the suitability of the mulberry and silkworm as an alternative method for the remediation of Cd-polluted soil; it also explored the underlying mechanisms regulating the trophic transfer of Cd. The results show that both the mulberry and silkworm have high Cd tolerance. The transfer factor suggests that the mulberry has high potential for Cd extraction from polluted soil. The subcellular distribution and chemical forms of Cd in mulberry leaves show that cell wall deposition and vacuolar compartmentalization play important role in Cd tolerance. In the presence of increasing Cd concentrations in silkworm food, detoxification mechanisms (excretion and homeostasis) were activated so that excess Cd was excreted in fecal balls, and metallothionein levels in the mid-gut, the posterior of the silk gland, and the fat body of silkworms were enhanced. And, the Cd concentrations in silk are at a low level, ranging from 0.02 to 0.21 mg kg⁻¹. Therefore, these mechanisms of detoxification can regulate Cd trophic transfer, and mulberry planting and silkworm breeding has high phytoremediation potential for Cd-contaminated soil.

The directive 2008/105/EC suggests the use of sediment or biota matrix for long-term monitoring of specific priority pollutants that tend to accumulate. But, the intermittent nature of flow in the majority of the Mediterranean rivers results in large variability of biological communities and especially fish, making advantageous the examination of pollution trend in sediment matrix and not in living organisms (biota). In this study, sediment environmental quality standards (EQSs) and sediment quality indicators (SQIs) were used to assess pollution by heavy metals (cadmium, nickel, lead, mercury, arsenic, chromium, copper, and zinc) and polycyclic aromatic hydrocarbons (PAHs) in Evrotas River, South Greece, monitored seasonally for 2 years (2009–2010) in five sampling sites. The results showed that, based on SQIs (geoaccumulation index (Igeo), enrichment factor (EF), and modified degree of contamination (mCd)), sediments of the Evrotas River can be classified as “low polluted,” with some exceptions of “extreme pollution.” EQS assessment revealed heavy metal pollution ranging from “low” to “medium high.” Furthermore, based on the Hakanson’s ecological risk index (RI) method, heavy metal potential risk was classified from “low” to “extreme.” Cadmium showed the highest RI values, while mercury reached “moderate” pollution level. The average ΣPAH concentration (24.4 ng g⁻¹) was lower than both the reported EQSs and the values found in literature for unpolluted or moderately polluted river sediments. Increased heavy metal and PAH concentrations were found in sites where mixing of freshwater with reclaimed water occurred. EQSs are suggested to be supplemented with the RI or EF index that consider the natural background to assist a first ecorisk assessment and should be foreseen by 2008/105/EC directive. Sediments can be considered as a valuable matrix in assessing the spatial and temporal trends of several contaminants and should be included in the monitoring program of temporary river management plans. Special attention should be given when defining reference sites and the sampling period. Decreasing flow period at the beginning of the spring prevailed in order to diminish any disturbance by flash flood events.

The large spatial heterogeneity in soil physico-chemical and microbial parameters challenges our ability to predict and model pesticide leaching from agricultural land. Microbial mineralization of pesticides is an important process with respect to pesticide leaching since mineralization is the major process for the complete degradation of pesticides without generation of metabolites. The aim of our study was to determine field-scale variation in the potential for mineralization of the herbicides glyphosate, bromoxyniloctanoate, diflufenican, and bentazone and to investigate whether this variation can be predicted by variations in basic soil parameters. Sixty-five soil samples were sampled from an agricultural, loamy field in Silstrup, Denmark, from a 60 × 165 m rectangular grid. The mineralization potential of the four pesticides was determined using a 96-well microplate ¹⁴C-radiorespirometric method. Initial mineralization rates were determined using first-order kinetics for glyphosate and bromoxyniloctanoate and zero-order kinetics for diflufenican and bentazone. The mineralization rates of the four pesticides varied between the different pesticides and the different soil samples, but we could not establish correlations between the pesticide mineralization rates and the measured soil parameters. Only the glyphosate mineralization rates showed slightly increasing mineralization potentials towards the northern area of the field, with increasing clay and decreasing OC contents. The mineralization potentials for glyphosate and bentazone were compared with 9-years leaching data from two horizontal wells 3.5 m below the field. The field-scale leaching patterns, however, could not be explained by the pesticide mineralization data. Instead, field-scale pesticide leaching may have been governed by soil structure and preferential flow events.

The objectives of the survey were to analyse the structure of the mollusc communities in the mining subsidence reservoirs that were created as a result of land subsidence over exploited hard coal seams and to determine the most predictive environmental factors that influence the distribution of mollusc species. The reservoirs are located in urbanised and industrialised areas along the Trans-Regional Highway, which has a high volume of vehicular traffic. They all have the same sources of supply but differ in the physical and chemical parameters of the water. In total, 15 mollusc species were recorded including four bivalve species. Among them Anodonta cygnea is classified as Endangered according to the Polish Red Data Book of Animals and also as Near Threatened according to the European Red List of Non-marine Molluscs. Eleven of the 15 mollusc species are included on the European Red List of Non-marine Molluscs as Least Concern. Conductivity, pH and the concentration of calcium were the parameters most associated with the distribution of mollusc species. Canonical correspondence analysis showed that Potamopyrgus antipodarum, Radix balthica, Physella acuta, Gyraulus crista and Pisidium casertanum were associated with higher conductivity and lower pH values. A. cygnea, Anodonta anatina and Ferrissia fragilis were negatively influenced by these parameters of the water. The results of this survey showed that the mining subsidence reservoirs located in urbanised and industrialised areas provide refuges for rare and legally protected species and that they play an essential role in the dispersal of alien species as well.

An erythromycin-degrading bacterium was isolated from the activated sludge of a sewage treatment plant (STP). Based on the morphological and physiological characteristics, the isolated strain was identified and named as Pseudomonas sp. ERY-E. In an inorganic salt medium inoculated at 1 % (v/v) of ERY-E strain containing 50 mg/L of erythromycin (ERY), the removal efficiency of ERY as high as 83.7 % was obtained under the optimum conditions with temperature of 30 °C, pH of 7.0, and 10 mg/L of yeast as the external carbon source. Subsequently, the ERY-E strain was used for bioaugmenting a biological aerated filter (BAF) to treat surface water containing low-concentration ERY. The influence of hydraulic retention time (HRT) and air-liquid ratio (A/L) on the performance of BAF was investigated. The average removal efficiencies of ERY and permanganate index (CODMₙ) were about 60.6 and 26.1 % in bioaugmented system (BAF₂) and 26.9 and 26.0 % in unbioaugmented system (BAF₁), respectively, under the optimum conditions with HRT of 4.0 h and A/L of 4:1 at steady state. Due to the stable removal of CODMₙ in BAF₂ as compared with BAF₁, it can be concluded that the introduction of ERY-E strain could collaborate with the indigenous microorganisms to attain a better ERY removal efficiency. As a result, the bioaugmented BAF method can be considered as an alternative technology for the treatment of surface water containing low-concentration emerging pollutants.

The effect of humic acid (HA), on the adsorption and transport of arsenic (As) onto and within a model iron oxide-based adsorbent, iron oxide-coated diatomite (IOCD), is investigated. Experimental results indicate that the adsorption of both As and HA is highly pH-dependent. As uptake was suppressed by HA, with the level of suppression increasing with HA concentration. The suppression is attributed to the partial coverage of the adsorption sites, as confirmed by elemental analysis. Adsorption energy analysis indicates that for As(III), the main interaction with IOCD is physical adsorption, whereas for As(V), it is more likely ion exchange. The presence of HA may alter the adsorption energy and interaction of As with the adsorbent, particularly at higher HA concentrations. Kinetic results indicate that HA did not affect the diffusional transport of As in systems with both As and HA. However, for IOCD preloaded with HA, the adsorption kinetics of As was significantly slower, although the As uptake was similar to the conditions of co-sorption with HA. The slower kinetics and similar equilibrium uptake of As in the HA-preloaded IOCD system may be attributed to the partial blockage of the intraparticular pores within IOCD, which slowed down the diffusion of As.

Early-life exposure to pollutants, such as lead, may have long-lasting consequences on health, behavior, and cognition. However, experiments on delayed effects of specific pollutants are very rare in wild animals. We experimentally exposed wild nestling great tits (Parus major) to dietary lead (high, low, or control group) in levels relevant to exposure levels of wild populations in Europe and studied delayed effects on phenotypic and behavioral traits in captivity. We also included a group of birds from a vicinity of a copper smelter, exposed to a mixture of toxic metals and altered food supply during development. This experimental setup allowed us to compare the strength of direct (exposure to lead per se) and indirect (pollution-related changes in diet) effects of pollutants. Our experimental lead treatment significantly increased lead levels in bone and feces compared with controls. However, we found no carry-over effect of early-life dietary lead on morphology, plumage coloration, or heat shock proteins. Treatment did not affect activity, exploration, neophobia, or success in learning and spatial memory task. We conclude that with the exposure levels and relatively short exposure period used, delayed effects on the measured traits were not found. However, it is important to further study other types of behavioral traits and ultimately fitness effects.

This study assessed the suitability of passive sampler extracts for use with a GC-MS-database rapid screening technique for around 940 organic chemicals. Chemcatcher™ passive sampler systems containing either Empore™ SDB-XC or C18FF disks were deployed at 21 riverine sites in and near Melbourne, Victoria, Australia, for a period of 28 days during September–October 2008. Methanolic elution of the SDB-XC and C18FF disks produced an extract that, after evaporation and inversion into hexane, was compatible with the GC-MS-database method enabling over 30 chemicals to be observed. The sources of the non-agricultural chemicals are still unclear, but this study was conducted in a relatively dry season where total rainfall was approximately 40 % lower than the long-term mean for the catchment during the study period. Thus, the risks may be greater in wetter seasons, as greater quantities of chemicals are likely to reach waterways as the frequency, extent and intensity of surface run-off events increase. This study provides valuable information for policy and decision-makers, both in Australia and other regions of the world, in that passive sampling can be conveniently used prior to analysis by multi-residue techniques to produce data to assess the likely risks trace organic chemicals pose to aquatic ecosystems.