Introduction Chlorimuron-ethyl has been widely used for the soybean production of China, but less information is available on the possible risk of long-term application of this herbicide. Materials and methods In this paper, soil samples were collected from the plots having been received 30 g active component of chlorimuron-ethyl/ha per year for 5 and 10 years in a continuously cropped soybean field of Northeast China, with their microbial community analyzed by plate counting, PCR-DGGE, and cloning library. Chlorimuron-ethyl had a higher accumulation in test soils, and the accumulation decreased the CFU of soil bacteria and increased the CFU of soil fungi significantly. The CFU of soil actinomycetes only had a significant decrease in the plot having been received chlorimuron-ethyl for 10 years. Results and discussion Under the long-term stress of chlorimuron-ethyl, the diversity and evenness of soil microbial community decreased, and more importantly, some bacterial and fungal species that possibly benefited soybean's growth, e.g., Acidobacteria, γ-proteobacteria, Cortinarius violaceu, Acarospora smaragdula, and Xerocomus chrysenteron decreased or demised, while some species that could induce the obstacle of soybean's continuous cropping, e.g., Fusarium oxysporum, Rhizoctonia solani, and Phytophthora sojae, increased or appeared. Some actinomycetes were inhibited having negative effects on the antagonism between soil microbes. It is considered that due to the longer half-life of chlorimuron-ethyl in soil and the resistance and resilience of soil microbes to short-term environmental stress, long-term in situ investigation rather than laboratory microcosm test or short-term field experiment would be more appropriate to the accurate assessment of the ecological risk of long-term chlorimuron-ethyl application. Further studies should be made on the application mode and duration of chlorimuron-ethyl to reduce the possible ecological risk of applying this herbicide on continuously cropped soybean field.

BACKGROUND: Soil samples from remote Alpine areas were analyzed for polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans and polychlorinated biphenyls by high-resolution gas chromatography/high-resolution gas spectrometry. Additionally, the EROD micro-assay and a genetically modified yeast estrogen bioassay were carried out to determine persistent aryl hydrocarbon receptors (AhR) and estrogen receptors (ER) agonists, respectively. Regarding the AhR agonists, the toxicity equivalents of analytical and EROD determined values were compared, targeting both altitude of samples and their soil organic content. The ratio between bioassay derived equivalents and analytical determinations suggested no significant contribution of unknown AhR inducers in these sampling sites and some antagonism in soils with relatively high PCB loading. More CYP1A1 expression was induced at the highest sites or about 1400–1500 m a.s.l. along the altitude profiles. Surprisingly, no clear tendencies with the soil organic content were found for dioxin-like compounds. Mean values obtained in the present study were for ER agonists, 0.37 ± 0.12 pg 17ß-estradiol EQ g⁻¹ dry soil and 6.1 ± 4.2 pg TCDD-EQ g⁻¹ dry soil for AhR agonists. CONCLUSION: Low bioassay responses with a higher relative amount of AhR inducers than ER disrupters were detected, indicating the higher abundance of persistent dioxin-like than estrogen-like compounds in these forested mountainous areas.

INTRODUCTION: It is predicted that demand for electricity in Islamic Republic of Iran will continue to increase dramatically in the future due to the rapid pace of economic development leading to construction of new power plants. At the present time, most of electricity is generated by burning fossil fuels which result in emission of great deal of pollutants and greenhouse gases (GHG) such as SO₂, NOₓ, and CO₂. The power industry is the largest contributor to these emissions. Due to minimal emission of GHG by renewable and nuclear power plants, they are most suitable replacements for the fossil-fueled power plants. However, the nuclear power plants are more suitable than renewable power plants in providing baseload electricity. The Bushehr Nuclear Power Plant, the only nuclear power plant of Iran, is expected to start operation in 2010. This paper attempts to interpret the role of Bushehr nuclear power plant (BNPP) in CO₂ emission trend of power plant sector in Iran. MATERIALS AND METHODS: In order to calculate CO₂ emissions from power plants, National CO₂ coefficients have been used. The National CO₂ emission coefficients are according to different fuels (natural gas, fuels gas, fuel oil). RESULTS AND DISCUSSION: By operating Bushehr Nuclear Power Plant in 2010, nominal capacity of electricity generation in Iran will increase by about 1,000 MW, which increases the electricity generation by almost 7,000 MWh/year (it is calculated according to availability factor and nominal capacity of BNPP). CONCLUSIONS: Bushehr Nuclear Power Plant will decrease the CO₂ emission in Iran power sector, by about 3% in 2010.

PURPOSE: Heterocyclic aromatic compounds containing nitrogen, sulfur, or oxygen heteroatoms (NSO-HET) have been detected in air, soil, marine, and freshwater systems. However, only few publications are available investigating NSO-HET using in vitro bioassays. To support better characterization of environmental samples, selected NSO-HET were screened for dioxin-like activity in two bioassays. METHODS: The present study focuses on the identification and quantification of dioxin-like effects of 12 NSO-HET using the DR-CALUX assay, and the 7-ethoxyresorufin-O-deethylase (EROD) assay with the permanent fish liver cell line RTL-W1. Changes of the total medium compound concentrations during the test procedure due to, e.g., sorption or volatilization were quantified using GC/MS. RESULTS: The NSO-HET benzofuran, 2,3-dimethylbenzofuran, dibenzofuran, dibenzothiophen, acridine, xanthene, and carbazole caused a response in the DR-CALUX assay. Only benzofuran and 2,3-dimethylbenzofuran were also positive in the EROD assay. All other compounds were inactive in the EROD assay. Relative potency (REP) values ranged from (2.80 ± 1.32) · 10−8 to (3.26 ± 2.03) · 10−6 in the DR-CALUX and from (3.26 ± 0.91) · 10−7 to (4.87 ± 1.97) · 10−7 in the EROD assay. CONCLUSIONS: The REP values were comparable to those of larger polycyclic aromatic hydrocarbons, e.g., fluoranthene and pyrene. Thus, and because of the ubiquitous distribution of heterocyclic aromatic compounds in the environment, the provided data will further facilitate the bioanalytical and analytical characterization of environmental samples towards these toxicants.

PURPOSE: The purpose this research is to investigate the interaction of Cr(VI) species, present as Cr₂O₇ ²⁻, at ambient temperature with brick clay pre-fired at different temperatures. METHODS: A multi-technique approach was used for this investigation. Experiments such as surface titrations, Langmuir and Freundlich adsorption isotherms, mass-firing temperature investigation, scanning electron microscopy, Fourier transform infrared spectra, X-ray fluorescence spectra, and X-ray diffraction were conducted in this investigation. RESULTS: Fired brick clay, which bears a negative charge according to surface titration measurements, shows affinity towards Cr(VI) species despite the negative charge of the source of Cr(VI). The Cr(VI)—brick clay heterogeneous system, which shows the strongest interaction with brick clay fired at 200°C, obeys both the Langmuir and the Freundlich adsorption isotherms with high regression coefficients. Investigation on surface charge, constituents of brick clay, acid treatment of clay particles, and the effect of firing temperature suggests that the reduction of Cr(VI) to Cr(III) by reducing agents present in brick clay makes a significant contribution for adsorption of chromium species followed by subsequent removal. Scanning electron microscopic images support the adsorption of chromium species, and further, many metal ions are released as a result of Cr(VI)—brick clay interaction according to X-ray fluorescence studies. CONCLUSION: It is concluded that fired brick clay shows strong adsorption capacity on Cr(VI), having the maximum interaction with brick clay fired at 200°C. It is proposed that this methodology be extended for treatment of effluents containing Cr(VI) species.

Background aim and scope The objective of the study was to determine the effects of ca. 35 years of pesticide contamination (pesticide dump--PD) of Lake Szeląg Wielki (located in the north-eastern Poland) on changes in the microbial communities of aquatic ecosystems. In the years 2008-2009, analyses were carried out for seasonal changes in the quantity and composition of bacterioplankton in the lake examined, which is of high significance to the tourism and fishing industries and is located in the vicinity of an area subjected to reclamation after a pesticide dump. Methods Bacterioplankton composition was assayed by fluorescence in situ hybridisation technique for the contribution of major groups of the Bacteria domain: ά-, β- and γ-Proteobacteria, Cytophaga-Flavobacterium and Actinobacteria as well as bacteria capable of degrading pesticides in an aquatic environment--Pseudomonas spp. Seasonal patterns of the total number of bacteria were determined by direct counting of 4′,6-diamidino-2-phenylindole (DAPI)-stained cells. Results The percentage of the detected Eubacteria (EUB 338 probe) relative to all the DAPI-stained bacteria in Lake Szeląg Wielki ranged from 46% to 63%. Bacteria capable of degrading pesticides in an aquatic environment--Pseudomonas spp.--were identified with a highly specific probe PEA 998. The highest mean values of this parameter reached 5.1%. In the spring, Pseudomonas spp. bacteria accounted for up to 80% of all Gamma-Proteobacteria microbes. Conclusion The study showed that the qualitative and quantitative changes in the bacterioplankton of the lake can be characterised by tendencies which are typical of a eutrophic water reservoir. However, a higher contribution of microorganisms capable of degrading sparingly degradable, toxic compounds and pesticides was determined in bacterioplankton from the PD-contaminated lake, as compared to microbial communities of a lake not contaminated with pesticides.

BACKGROUND AND SCOPE: Effect-directed analysis is increasingly used for the identification of key toxicants in environmental samples and there is a growing need for in vivo biotests as diagnostic tools. Within this study, we performed an in vivo sediment contact test, applicable on both native field samples and their extracts or fractions, in order to be able to compare the results from both field and laboratory studies. MATERIAL AND METHODS: A sediment contact test with the prosobranch snail, Potamopyrgus antipodarum, was carried out on extracts and fractions of field sediments from three European river basins. The results were compared with previous results of the native field samples. RESULTS: In contrast to the native sediments, the extracts of the samples led to an overall decrease in reproduction. Even the chosen reference sites had an adverse effect on the snails' reproduction. It appeared that a higher bioavailability in the organic extracts, together with a changing composition of compounds could have lead to this change in effects. The fractionation of the extracts partly led to a more differentiated picture, but the resolution was not high enough to see any distinct effects on the snails' reproduction. DISCUSSION AND CONCLUSION: Our results highlight the importance of the use of in vivo biotests and point out the relevance of bioavailability in native sediments. For further fractionation studies, a more realistic extraction procedure, together with a higher resolution fractionation, would be appropriate in order to separate individual bioavailable compounds more efficient.

INTRODUCTION: Through leaching experiments and simulated rainfall experiments, characteristics of vertical leaching of exogenous rare earth elements (REEs) and phosphorus (P) and their losses with surface runoff during simulated rainfall in different types of soils (terra nera soil, cinnamon soil, red soil, loess soil, and purple soil) were investigated. RESULTS AND ANALYSES: Results of the leaching experiments showed that vertical transports of REEs and P were relatively low, with transport depths less than 6 cm. The vertical leaching rates of REEs and P in the different soils followed the order of purple soil > terra nera soil > red soil > cinnamon soil > loess soil. Results of the simulated rainfall experiments (83 mm h⁻¹) revealed that more than 92% of REEs and P transported with soil particles in runoff. CONCLUSION: The loss rates of REEs and P in surface runoff in the different soil types were in the order of loess soil > terra nera soil > cinnamon soil > red soil > purple soil. The total amounts of losses of REEs and P in runoff were significantly correlated.

Background and aim Many rivers have to receive treated or untreated wastewater as the main water sources in the world, especially in the countries facing with water shortage. For instance, the Haihe and Huaihe River Basin, which are among areas facing crises for water resources in China, receive 33,400 million tons of wastewater per year. As the sediment has large capacity for sorbing hydrophobic organic pollutants such as polycyclic aromatic hydrocarbons (PAHs), it can act as a natural repository for the contaminants. This means pollutants can release into water phase again under some conditions, such as resuspension, sediment dredging, etc. The objective of this research was to study the trends of PAH release from sediments in rivers receiving much wastewater, such as Yongding New River (YD), Northsewer (NS), and Southsewer (SS) from Haihe River Basin. These rivers received most of the wastewater from Tianjin, China and merge into Bohai Bay finally. Methods Sediments (namely YD, NS, and SS) were collected from Yongding New River, Northsewer, and Southsewer, respectively. The physical and chemical properties of the sediments, including particle size distribution, total organic carbon (TOC) and black carbon (BC) contents, elemental compositions, organic functional groups analyzed from Fourier transformed infrared (FTIR), and nuclear magnetic resonance (NMR) spectra, were characterized. PAH desorption from the sediments was measured with the Tenax shaken slurry desorption method. Results The NS sediment had a greatly higher TOC and BC contents, while lower BC-to-TOC ratio than YD and SS sediments. NMR and FTIR analysis showed that aliphatic carbons were more abundant in NS sediment than SS sediment. The desorption experiments showed that PAHs desorbed more rapidly from YD and NS sediments than from SS sediment. PAH fraction desorbed after each interval during the experiment except 0.8 day was significantly correlated with PAH properties among all the three sediments. Discussion The higher BC-to-TOC ratio in SS sediment corresponded to slower desorption rate and less desorption extent of PAHs from SS sediment among the three sediments. This probably could be explained by the extremely strong sorption ability of BC. It also proved that the sequestration of PAHs in sediment was not simply the result of higher organic carbon content. Conclusions Considering the physical and chemical characterization of the sediments and PAH desorption properties comprehensively, BC-to-TOC ratio was a more important factor controlling the behavior of PAHs in sediments than absolute TOC or BC content.

BACKGROUND, AIM, AND SCOPE: Ferro-cyanide is one of the commonly found species at cyanide-contaminated soils and groundwater. Unlike botanical metabolism of KCN via the β-cyanoalanine pathway, processes involved in the plant-mediated assimilation of ferro-cyanide are still unclear. The objective of this study was to investigate a possible mechanism involved in uptake and assimilation of ferro-cyanide by plants. MATERIALS AND METHODS: Detached roots of plants were exposed to ferro-cyanide in a closed-dark hydroponic system amended with HgCl2, AgNO3, LaCl3, tetraethylammonium chloride (TEACl), or Na3VO4, respectively, at 25 ± 0.5°C for 24 h. Total CN, free CN-, and dissolved Fe2+ were analyzed spectrophotometrically. Activity of β-cyanoalanine synthase involved in cyanide assimilation was also assayed using detached roots of plants in vivo. RESULTS: Dissociation of ferro-cyanide [FeII(CN)6]-4 to free CN- and Fe2+ in solution was negligible. The applied inhibitors did not show any significant impact on the uptake of ferro-cyanide by soybean (Glycine max L. cv. JD 1) and hybrid willows (Salix matsudana Koidz × alba L.; p > 0.05), but rice (Oryza sativa L. cv. JY 98) was more susceptible to the inhibitors compared with the controls (p < 0.05). However, TEACl had the most severe effect on the assimilation of ferro-cyanide by soybean, hybrid willows, and maize (Zea mays L. cv. PA 78; p < 0.01), whereas AgNO3 was the most sensitive inhibitor to rice (p < 0.01). No measurable difference in β-cyanoalanine synthase activity of roots exposed to ferro-cyanide was observed compared with the control without any cyanides (p > 0.05), whereas roots exposed to KCN showed a considerable increase in enzyme activity (p < 0.05). CONCLUSIONS: Plants take up Fe2+ and CN- as a whole complex, and in vivo dissociation to free CN- is not prerequisite during the botanical assimilation of ferro-cyanide. Ferro-cyanide is likely metabolized by plants directly through an unknown pathway rather than the β-cyanoalanine pathway.