The present study aims to investigate the EDTA catalyzed reduction of nitrate (NO 3 − ) by zero-valent bimetallic (Fe–Ag) nanoparticles (ZVBMNPs) in aqueous medium and to enumerate the effect of temperature, solution pH, ZVBMNPs dose and EDTA concentration on NO 3 − reduction. Batch experimental data were generated using a four-factor Box–Behnken design. Optimization modeling was performed using the response surface method for maximizing the reduction of NO 3 − by ZVBMNPs. Significance of the independent variables and their interactions were tested by the analysis of variance and t test statistics. The model predicted maximum reduction capacity (340.15 mg g−1 NO 3 − ) under the optimum conditions of temperature, 60 °C; pH 4; dose, 1.0 g l−1; and EDTA concentration, 2.0 mmol l−1 was very close to the experimental value (338.62 mg g−1) and about 16 % higher than the experimentally determined capacity (291.32 mg g−1). Study demonstrated that ZVBMNPs had higher reduction efficiency than Fe0 nanoparticles for NO 3 − . EDTA significantly enhanced the NO 3 − reduction by ZVBMNPs. The EDTA catalyzed reduction of NO 3 − by ZVBMNPs can be employed for the effective decontamination of water.

INTRODUCTION: Concentrations of alkylphenolic compounds (APCs) in water and sediments were related to the composition and functional descriptors of the benthic community (biofilm and macroinvertebrates). MATERIALS AND METHODS: Samples were collected in four sampling campaigns at seven sampling points in the lower Llobregat catchment area (NE Spain). Water and sediment samples underwent chemical target analysis for nine APCs, which are known to disrupt the endocrine system. RESULTS AND DISCUSSIONS: APCs were the main stressors on the diatom community but not on the macroinvertebrate community. CONCLUSIONS: Benthic invertebrates were mostly affected by the general physicochemical water characteristics (where conductivity was a surrogate). Nonylphenol only had an influence on the diatom community in water but not in the remaining compartments, probably because of the low concentrations observed in the environment.

This study investigated the effects of pH (6–10) and ozone dose [0.4–3.0 mg O3/mg dissolved organic carbon (DOC)] on the content and structure of haloacetic acid (HAA) precursors in groundwater rich in natural organic matter (NOM; DOC 9.85 ± 0.18 mg/L) during drinking water treatment. The raw water was ozonated in a 2 L glass column. NOM fractionation was carried out using XAD resins. HAA formation potential (HAAFP) was determined according to standard EPA Method 552. NOM characterization revealed it is mostly hydrophobic (65 % fulvic and 14 % humic acids). Hydrophobic NOM significantly influences HAA formation, as confirmed by the high HAAFP (309 ± 15 μg/L). Ozonation at pH 6–10 led to changes in NOM structure, i.e. complete humic acid oxidation, and increased the hydrophilic NOM fraction content (65–90 % achieved using 3.0 mg O3/mg DOC). The highest degree of NOM oxidation and HAA precursor removal was achieved at pH 10 (up to 68 % HAAFP). Ozonation pH influenced the distribution of HAA precursor content, as increasing the pH from 6 to 10 increased the reactivity of the hydrophilic fraction, with the HAAFP increasing from 19.1 ± 6.0 μg/mg DOC in raw water to 152 ± 8 μg/mg DOC in ozonated water. The degree of HAA precursor removal depends on the dominant oxidation mechanism, which is related to the applied ozone dose and the pH of the oxidation process. Ozonation at pH 10 favours the mechanism of radical NOM oxidation and was the most effective for HAAFP reduction, with the efficacy of the process improving with increasing ozone dose.

INTRODUCTION: The toxic effect of the oxidation hair dyes on Phanerochaete chrysosporium was investigated by exposure of this fungus in a nitrogen-limited culture medium to various concentrations of the oxidation hair dyes. RESULTS: The results showed that both the size and the dry weight of the mycelial pellets of P. chrysosporium could be reduced when the concentration of the oxidation hair dyes was higher than 300 mg/L. By using the AFLP analysis and the UPGMA dendrogram, the DNA damage of P. chrysosporium by the oxidation hair dyes was also detected. Comparing with that in the control, the percent polymorphism under different concentrations of the oxidation hair dyes increased. In the meantime, the DNA similarity was decreased, which meant that the DNA damage was aggravated with an increase in the concentrations of the oxidation hair dyes. CONCLUSION: Thus, as an environmental pollutant, the oxidation hair dyes have a toxic effect on P. chrysosporium at both cellular and molecular levels.

INTRODUCTION: In Egypt, the picture of threats to humans and the environment from the exposure to organic pollutants is still incomplete. Thus the objectives of this study were to assess the occurrence and distribution of polychlorinated biphenyls (PCBs), organochlorine pesticides, and chlorpyrifos in sediments and mussels of Abu Qir Bay and their risks for environment and human health. MATERIALS AND METHODS: Twenty-three different compounds organochlorines were determined in 20 surfacial sediment and 10 mussel samples by gas chromatography-electron capture detector. A Screening Level Ecological Risk Assessment (SLERA) and a Human Health Risk Assessment (HHRA) were performed with the data. RESULTS AND DISCUSSION: ΣDDT (DDT, DDE, DDD) (average concentration 27 µg/kg dw) dominated the detected organic pollutants in the sediments, followed by CHLs (chlordane, heptachlor, heptachloro epoxide), hexachlorocyclohexane, chlorpyrifos, endosulfane, dieldrine, Σ6 PCBs, aldrine, hexachlorobenzene, pentachlorobenzene, methoxychlor, and mirex. In general, concentrations of Σ6 PCBs in mussels were higher than their corresponding sediment concentrations reflecting their relatively high bioavailability and bioaccumulative potential. However, concentrations of the organochlorine pesticides in mussels were lower than their corresponding sediment samples. Nevertheless, the SLERA on the bay sediments revealed that adverse ecological effects to benthic species are expected to occur whereas the HHRA showed that adverse health effects are not expected to occur from the consumption of the mussels. CONCLUSIONS: With the help of a SLERA, it was possible to indicate which class of chlorinated organic compounds is of highest concern to assess and to improve the environmental quality of the bay. Monitoring of organochlorines and chlorpyrifos would be needed to control the future trend of pollution.

INTRODUCTION: The accelerated biodegradation of 3-nitrophenol (3-NP) in the rhizosphere of giant duckweed (Spirodela polyrrhiza) was investigated. MATERIALS AND METHODS: Biodegradation of 3-nitrophenol in the rhizosphere of a floating aquatic plant, S. polyrrhiza, was investigated by using three river water samples supplemented with 10 mg l−1 of 3-NP. Isolation and enrichment culture of 3-NP-degrading bacteria were performed in basal salts medium containing 3-NP (50 mg l−1). The isolated strains were physiologically and phylogenetically characterized by using an API20NE kit and 16S rRNA gene sequencing. RESULTS AND DISCUSSION: Accelerated removal of 3-NP (100%) was observed in river water samples with S. polyrrhiza compared with their removal in plant-free river water. Also, 3-NP persisted in an autoclaved solution with aseptic plants, suggesting that the accelerated 3-NP removal resulted largely from degradation by bacteria inhabiting the plant rather than from adsorption and uptake by the plant. We successfully isolated six and four strains of 3-NP-degrading bacteria from the roots of S. polyrrhiza and plant-free river water, respectively. Phylogenetic analysis based on 16S rRNA gene divided the 3-NP-degrading bacteria into two taxonomic groups: the genera Pseudomonas and Cupriavidus. The strains belonging to the genus Cupriavidus were only isolated from the roots of duckweed. All strains isolated from the roots utilized 3-NP (0.5 mM) as a sole carbon and energy source, indicating that they could have contributed to the accelerated degradation of 3-NP in the rhizosphere of S. polyrrhiza. CONCLUSIONS: The rhizoremediation using S. polyrrhiza and its rhizosphere bacteria can be an effective strategy for cleaning up the 3-NP-contaminated surface waters.

INTRODUCTION: Initial geosmin degradation was closely related to water temperature and natural geosmin concentration of sampling environment. Here, for the first time, we evaluated the biodegradation of geosmin by microorganisms in biofilm from biological treatment unit of actual potable water treatment plant. MATERIALS AND METHODS: At an initial geosmin concentration of 2,500 ng/l, efficient geosmin removal was confirmed throughout the year. Furthermore, in the presence of mixed musty odor compounds (geosmin and MIB) as carbon source, geosmin degradation was enhanced compared to sole carbon source (geosmin alone). RESULTS AND DISCUSSION: PCR-DGGE analysis revealed a rich community structure within the biofilm during rapid geosmin removal period, April. PCA revealed that the significant change in bacterial communities occurred from day 1 to day 2. Two novel geosmin-degrading bacteria were isolated from the biofilm of the biological treatment unit of Kasumigaura Water Purification, Waterworks Department, Japan. They belong to Methylobacterium sp. and Oxalobacteraceae bacterium, respectively. CONCLUSIONS: These studies provide further insights into the unknown microbiological processes that occur during the biological removal of geosmin through water treatment and could facilitate the geosmin bioremediation in contaminated habitats.

Chaohu Lake, one of the most eutrophicated lakes in China, has been suffering from long-term outside pollution, urban sewage, river outflows, and agricultural runoff which expectedly have been the main contributors of hydrocarbons. However, the contributions from these various sources have not been specified. The present study is aimed at identifying the potential sources of hydrocarbons in surface sediment around the whole lake and assessing the relative contributions using principal components analysis–multiple linear regression (PCA-MLR). Sixty-one surface sediments covering the whole Chaohu Lake and three main estuaries of inflowing rivers were collected, dried, extracted, and analyzed for 27 normal alkanes (n-alkanes, from C12 to C38, defined Σ27AH) and unresolved complex mixture (UCM) by GC/MS. Diagnostic ratios and PCA-MLR were utilized to apportion their sources. The concentrations of Σ27AH and UCM ranged from 434 to 3,870 ng/g and 11.9 to 325 μg/g dry weight, respectively, for all samples. The concentrations of Σ27AH in western region and estuary of Nanfei River were slightly higher but without statistical significance than those from eastern region and estuaries of Yuxi River and Hangbu River. The concentration of UCM from western region was significantly higher than that obtained from eastern region. These results reflect the importance of input of urban runoff by Nanfei River and serious eutrophication in western region. Aliphatic hydrocarbons in Chaohu Lake were mainly derived from high plant wax with mixed sources of phytoplankton and petroleum. Weak microbial decomposition of n-alkanes would be expected to occur from the low ratios of isoprenoid hydrocarbons pristine (pri) and phytane (phy) to n-C17 and n-C18, respectively. Higher plant, fossil combustion, petroleum residue, and phytoplankton were proposed as the main origines of aliphatic hydrocarbons by PCA while the contributions of individual n-alkane homologues, pri and phy from the identified sources (31 % from higher plant, 30 % from fossil combustion, 26 % from petroleum, and 19 % from phytoplankton) were well predicted using MLR. The distribution profile and corresponding diagnostic ratios of normal alkanes show the promising potential as a useful proxy for estimating the source and loading of pollutants in Chaohu Lake.

BDE-47 is one of the most widely found congeners of PBDEs in marine environments. The potential immunomodulatory effects of BDE-47 on fish complement system were studied using the marine medaka Oryzias melastigma as a model fish. Three-month-old O. melastigma were subjected to short-term (5 days) and long-term (21 days) exposure to two concentrations of BDE-47 (low dose at 290 ± 172 ng/day; high dose at 580 ± 344 ng/day) via dietary uptake of BDE-47 encapsulated in Artemia nauplii. Body burdens of BDE-47 and other metabolic products were analyzed in the exposed and control fish. Only a small amount of debrominated product, BDE-28, was detected, while other metabolic products were all under detection limit. Transcriptional expression of six major complement system genes involved in complement activation: C1r/s (classical pathway), MBL-2 (lectin pathway), CFP (alternative pathway), F2 (coagulation pathway), C3 (the central component of complement system), and C9 (cell lysis) were quantified in the liver of marine medaka. Endogenous expression of all six complement system genes was found to be higher in males than in females (p < 0.05). Upon dietary exposure of marine medaka to BDE-47, expression of all six complement genes were downregulated in males at day 5 (or longer), whereas in females, MBl-2, CFP, and F2 mRNAs expression were upregulated, but C3 and C9 remained stable with exposure time and dose. A significant negative relationship was found between BDE-47 body burden and mRNA expression of C1r/s, CFP, and C3 in male fish (r = −0.8576 to −0.9447). The above findings on changes in complement gene expression patterns indicate the complement system may be compromised in male O. melastigma upon dietary exposure to BDE-47. Distinct gender difference in expression of six major complement system genes was evident in marine medaka under resting condition and dietary BDE-47 challenge. The immunomodulatory effects of BDE-47 on transcriptional expression of these complement components in marine medaka were likely induced by the parent compound instead of biotransformed products. Our results clearly demonstrate that future direction for fish immunotoxicology and risk assessment of immunosuppressive chemicals must include parallel evaluation for both genders.

Phosphorus concentration in rivers results from both external inputs and internal loading from the bottom sediments. Seasonal, spatial, and multi-annual dynamics of phosphorus forms in bottom sediments and their interstitial water for the river Prut (Moldova) were evaluated. In order to determine content of total phosphorus in the bottom sediments, fresh (wet) samples were subjected to persulfate oxidation. The content of inorganic phosphorus was determined after acidic oxidation of samples. The amount of organic phosphorus was obtained by subtracting inorganic phosphorus from the amount of total phosphorus. Content of phosphorus forms in interstitial water was determined after centrifugation of fresh (wet) sediments. In general, the shape of dynamics of the amounts of inorganic phosphorus in sediments was close during years 2009, 2010, and 2011, with registered higher contents of this form on the middle course of the river. The spatial dynamics of organic phosphorus is less homogeneous along the Prut River. During 2009, higher amounts of organic phosphorus were recorded on the middle sector. During the spring of year 2010, the content of organic phosphorus in sediments was practically not changed along the river. The ratio of inorganic/organic phosphorus in bottom sediments was similar during the researched years, with the predominance of the inorganic phosphorus being recorded. Also, the increasing tendency of the percentage of organic phosphorus from spring to summer was identified. Generally, appropriate spatial and seasonal dynamics of phosphorus forms in bottom sediments and their interstitial water were recorded, although sometimes with some differences.