BACKGROUND, AIM AND SCOPE: The Pego-Oliva Marsh is the second most important wetland in the Valencian Community (Spain). It is included in the RAMSAR agreement and represents one key point for migratory birds. Emerging contaminants from the human pressure, such as pharmaceuticals, illicit drugs and personal care product, are not included in the list of priority contaminants of the Water Framework Directive yet, and are neither monitored nor controlled. However, pollution of emerging contaminants can threaten the environment and even human health. In order to understand the status of the emerging contamination and recommend future rationalization of countermeasures, the occurrence of illicit drugs was investigated. MATERIAL AND METHODS: Samples were collected at 23 sites from the main irrigation channels and the marsh. Illicit drugs were extracted using solid phase extraction and determined by liquid chromatography tandem mass spectrometry. The method detection limits ranged from 0.01 to 1.54 ng l−1 and the recoveries from 57% to 120%. RESULTS AND DISCUSSION: 3,4-Methylenedioxymethamphetamine, ketamine, morphine, benzoylecgonine, cocaine, methadone, 6-acetylmorphine and nor-9-carboxy-tetrahydrocannabinol were detected. The mean concentrations were 0.62, 21.33, 1.30, 1.92, 2.25, 0.32, 0.04 and 0.07 ng l−1, respectively. The highest concentrations were in the north of Pego-Oliva Marsh. CONCLUSIONS: The pollution status by illicit drugs of the Pego-Oliva Marsh has been established. However, contamination levels in all the area of the natural park were low compared with those reported in other superficial waters.

Di-isopropylnaphthalene (DIPN) has highly persistent and bioaccumulative properties, and a large amount of DIPN is used as a PCB substitute in Japan. However, DIPN in the environment has not been thoroughly investigated. In addition, mono-isopropylnaphthalene (MIPN) and tri-isopropylnaphthalene (TIPN), which are the homologues of DIPN, have similar properties to DIPN. In this study, simultaneous analytical methods for MIPN, DIPN, and TIPN for air, environmental water, sediment, and biological samples were developed, and the resultant contamination caused by each in the environment was investigated. DIPN was detected at 1.1 ± 0.38 ng/m3 in air and between < 1.9 and 9.8 ng/L in river water, but MIPN and TIPN were not. In Lateolabrax japonicas (Japanese sea perch), TIPN was detected from only females at between 0.65 and 1.4 ng/g-wet. DIPN was detected from all perches at between 1.2 and 3.4 ng/g-wet. DIPN and TIPN isomer fingerprints in females were different from those in the reference standard stock solution ones. In sediments, MIPN, DIPN, and TIPN were detected at between < 0.16 and 8.6 ng/g-dry, between < 1.1 and 4400 ng/g-dry, and between < 0.83 and 500 ng/g-dry, respectively. The contamination trend of DIPN in the sediments was similar to that of PCBs.

INTRODUCTION: Trends in precipitation pH and conductivity during 1992–2009, and in ionic compositions from January 2007 to June 2009, are reported from Lushan Mountain, one of the highest mountains in mid-east China. Annual mean pH was in the range of 4.35–5.01 and showed a statistically very significant (P < 0.01) decreasing trend with time. Annual mean conductivity showed a statistically significant (P < 0.05) increasing trend, although this was not the case for non-H conductivity. Increasing rainwater acidity was mainly caused by increasing amounts of acid substances entering the rain. The trends in precipitation pH and conductivity were directly associated with energy consumption. RESULTS AND DISCUSSIONS: Over the period of study, Lushan Mountain received more rainfall in spring and summer. The pH values varied seasonally with winter minima. The winter multiyear seasonal mean pH was 4.35. The corresponding summer value was 4.88. SO 4 2− and NO 3 − were the main anions, and NH 4 + and Ca2+ the main cations. The anion to cation ratio was 0.8–1.0, and that of [SO 4 2− ] to [NO 3 − ] was 2.4-3.0, much lower than that of the 1980s. However, sulfuric acid was still the main acid present. The ratio of [NH 4 + ] to [Ca2+] was about 1.0, suggesting that these two alkaline substances provided close acid neutralizing capacity. The ratio of [Cl−] to [Na+] was about 0.67, somewhat lower than that of natural precipitation. CONCLUSIONS: Ionic composition varied seasonally and was closely correlated to the amounts of rainfall and pollution. Trajectory analyses showed that the trajectories to Lushan Mountain could be classified in six clusters and trajectories originating from the South Sea and the areas surrounding Lushan Mountain had the greatest impacts on precipitation chemistry.

Bioaugmentation for the removal of polyaromatic hydrocarbons (PAHs) from wastewater using bacteria and yeasts is considered environment-friendly and a cost-effective technique. The effectiveness of this biodegradation system depends on the stability of inoculated microorganisms and the availability of nutrients. This study is aimed to investigate the removal of high molecular weight (HMW)-PAHs from biologically treated produced water using different biological systems. Three systems, inoculated with activated sludge (AS), the mixture of five yeast strains (MY), and the mixture of AS and the five yeast strains (SY), respectively, were constructed, and their performance for the removal of HMW-PAHs was compared over 10 weeks. The effluent of the biologically treated produced water from an oilfield was used as the influent after chrysene and benzo(a)pyrene were spiked as HMW-PAHs. Polymerase chain reaction-based denaturing gradient gel electrophoresis (PCR-DGGE) and fluorescent in situ hybridization (FISH) techniques were used to examine the changes in the structures and abundances of the bacterial and yeast communities in these three systems. Only SY and MY systems were capable to remove chrysene (90.7 % and 98.5 %, respectively) and benzo(a)pyrene (80.7 % and 95.2 %, respectively). PCR-DGGE analysis confirmed that all of the five yeast strains inoculated remained in the SY and MY systems, while FISH results showed that the relative abundance of yeast in the SY and MY systems (10.6 % to 21.9 %, respectively) were significantly higher than AS system (2.3 % to 7.8 %, respectively). The relative abundances of the catechol 2,3-dioxygenase (C23O) indicated that the copy number ratios of benzene ring cleavage gene C23O in the yeast amended systems were much higher than that in the AS system. In this study, all of the three systems were effective in removing the low molecular weight (LMW)-PAHs, while HMW-PAHs including chrysene and benzo(a)pyrene were efficiently removed by MY and SY systems, not by AS system. The high HMW-PAHs removal in the MY and SY bioaugmentation systems possibly attributed to the inoculation of the mixed yeast culture. By combining the PCR-DGGE results with the FISH analyses, it was found that yeast probably consisting mainly of the five inoculated strains inhabited in the two bioaugmentation systems as a dominant population. The relatively higher performance of the SY system might be attributed to the suspended growth type which permitted a more efficient contact between microbial cells and contaminants. The bioaugmentation systems (SY and MY) were successfully established by inoculating with five nonindigenous yeast strains and demonstrated high performance in removal of HMW-PAHs.

BACKGROUND AND PURPOSES: The pathways used by microorganisms for the metabolism of every xenobiotic substrate are specific. The catabolism of a xenobiotic goes through a series of intermediate steps and lower intermediates (metabolites) appear in sequence. The structure of the metabolites can be similar to the parents due to kinship. The purposes of this study were to examine if the degradation pathways that were developed for a parent xenobiotic are effective to degrade the parent’s lower metabolites, and if the reverse is true. MATERIALS AND METHODS: The xenobiotic substrates, 2,4-dichlorophenoxyacetic acid (2,4-D, the parent xenobiotic) and its metabolite 2,4-dichlorophenol (2,4-DCP), were independently subjected to acclimation and degradation tests by the biomasses of mixed-culture activated sludge and a pure culture of Arthrobacter sp. RESULTS: Activated sludge and Arthrobacter sp. that were acclimated to 2,4-D effectively degraded 2,4-D and the lower metabolites of 2,4-D, typically 2,4-DCP. During the degradation of 2,4-D, accumulations of the lower metabolites of 2,4-D were not found. The degradation pathways acquired from acclimation to 2,4-D are effective for all the metabolites of 2,4-D. However, pathways acquired from acclimation to 2,4-DCP are not effective in the degradation of the parent 2,4-D. CONCLUSIONS: Microorganisms acclimated to 2,4-D evolve their degradation pathways by a scheme that is different from the scheme the microorganisms employ when they are acclimated to the metabolites of 2,4-D.

PURPOSE AND AIM: Removal of an anionic azo dye Brilliant Yellow has been carried out from its aqueous solutions by using hen feathers as potential adsorbent. MATERIALS AND METHODS: Hen feathers procured from local poultry were cut, washed, and activated. Detailed chemical and physical analysis of hen feathers and its characterization through scanning electron microscopy, X-ray diffraction, and infrared measurements have been made. Procured dye has been adsorbed over under batch measurements and adsorption process is monitored using UV spectrophotometer. RESULTS: Optimum parameters for the adsorption of Brilliant Yellow over hen feathers have been determined by studying the effect of pH, temperature, concentration of dye, and amount of adsorbent. On the basis of Langmuir adsorption, isotherms feasibility of the ongoing adsorption has been ascertained and thermodynamic parameters have been calculated. Attempts have also been made to verify Freundlich, Tempkin, and Dubinin–Radushkevich adsorption isotherm models. It is found that during adsorption, uniform distribution of binding energy takes place due to interaction of the dye molecules and the ongoing adsorption process is chemisorptions. The kinetic measurements indicate dominance of pseudo-second-order process during the adsorption. The mathematical treatment on the kinetic data reveals the rate-determining step to be governed through particle diffusion at 8 × 10−5 M and involvement of film diffusion mechanism at higher concentration at temperatures at all the temperatures. CONCLUSIONS: The developed process is highly efficient and it can be firmly concluded that hen feather exhibits excellent adsorption capacity towards hazardous azo dye Brilliant Yellow.

PURPOSE: The objective of this paper is to assess the regulation of the accumulation of heavy metals in the aquatic environment and different fish species. METHODS: Water and fish samples were collected from upper to lower reaches of the Yangtze River. The heavy metal (Cd, Cr, Cu, Hg, Pb, Zn) concentrations in the muscle tissue of seven fishes were measured. Additionally, the relationships between heavy metal concentrations in fish tissue and fish size (length and weight), condition factor, water layer distribution, and trophic level were investigated. RESULTS: Metal concentrations (milligrams per kilogram wet weight) were found to be distributed differently among different fish species. The highest concentrations of Cu (1.22 mg/kg) and Zn (7.55 mg/kg) were measured in Pelteobagrus fulvidraco, the highest concentrations of Cd (0.115 mg/kg) and Hg (0.0304 mg/kg) were measured in Silurus asotus, and the highest concentrations of Pb (0.811 mg/kg) and Cr (0.239 mg/kg) were measured in Carassius auratus and Cyprinus carpio. A positive relationship was found between fish size and metal level in most cases. The variance of the relationships may be the result of differences in habitat, swimming behavior, and metabolic activity. In this study, fishes living in the lower water layer and river bottom had higher metals concentrations than in upper and middle layers. Benthic carnivorous and euryphagous fish had higher metals concentrations than phytoplankton and herbivorous fish. Generally, fish caught from the lower reach had higher metals concentrations than those from the upper reach. CONCLUSIONS: Cadmium and lead concentrations in several fishes exceeded the permissible food consumption limits, this should be considered to be an important warning signal.

INTRODUCTION: The present work is aimed to understand direct radiation effects due to aerosols over Delhi in the Indo-Gangetic Basin (IGB) region, using detailed chemical analysis of surface measured aerosols during the year 2007. METHODS: An optically equivalent aerosol model was formulated on the basis of measured aerosol chemical compositions along with the ambient meteorological parameters to derive radiatively important aerosol optical parameters. The derived aerosol parameters were then used to estimate the aerosol direct radiative forcing at the top of the atmosphere, surface, and in the atmosphere. RESULTS: The anthropogenic components measured at Delhi were found to be contributing ∼72% to the composite aerosol optical depth (AOD0.5 ∼0.84). The estimated mean surface and atmospheric forcing for composite aerosols over Delhi were found to be about −69, −85, and −78 W m−2 and about +78, +98, and +79 W m−2 during the winter, summer, and post-monsoon periods, respectively. The anthropogenic aerosols contribute ∼90%, 53%, and 84% to the total aerosol surface forcing and ∼93%, 54%, and 88% to the total aerosol atmospheric forcing during the above respective periods. The mean (±SD) surface and atmospheric forcing for composite aerosols was about −79 (±15) and +87 (±26) W m−2 over Delhi with respective anthropogenic contributions of ∼71% and 75% during the overall period of observation. CONCLUSIONS: Aerosol induced large surface cooling, which was relatively higher during summer as compared to the winter suggesting an increase in dust loading over the station. The total atmospheric heating rate at Delhi averaged during the observation was found to be 2.42 ± 0.72 K day−1, of which the anthropogenic fraction contributed as much as ∼73%.

BACKGROUND AND AIMS: Because of the widespread use of pesticides for domestic and industrial applications, the evaluation of their toxic effects is of major concern to public health. The aim of the present study was to investigate the propensity of dimethoate (DM), an organophosphorus pesticide, to cause oxidative damage in the liver and kidney of mice and its associated genotoxic effect. METHODS: DM was administered intraperitoneally at doses of 1, 5, 10, 15, and 30 mg/kg body weight for 30 consecutive days in BALB/c mice. Oxidative stress was monitored in the kidney and liver by measuring malondialdehyde level, protein carbonyl concentration, and the catalase activity. The genotoxicity of DM was assessed by the comet assay in vivo. RESULTS AND DISCUSSION: Our results indicated that DM inhibited acetylcholinesterase activities in the liver and kidney of treated mice. DM increased lipid peroxidation and protein carbonyl levels in the liver and kidney in a dose-dependent manner. Catalase activity was found to be significantly increased in the liver and kidney at doses higher than 5 mg/kg body weight. CONCLUSIONS: Our study demonstrated that DM induced DNA damage in the liver and kidney of treated mice in a dose-dependent manner; this induction was associated to DM-induced oxidative stress. Further investigations are needed to prove the implication of oxidative stress in genotoxicity induced by DM.

INTRODUCTION: Artisanal fisheries in tropical estuaries are an important economic activity worldwide. However, gear (e.g. ropes, nets, buoys, crates) and vessels are often in use under dangerous conditions. Polyfilament nylon ropes are used until they are well beyond human and environmental safety limits. Severe wear and tear results in the contamination of the environment with micro-fragments. The spread of these fragments in the marine environment and their ingestion by the biota are documented in the scientific literature and are increasing concerns. The aim of this study was to evaluate the ingestion of plastic fragments by two fish (drum) species in relation to seasonal, habitat and fish size–class variation. MATERIALS AND METHODS: The stomach contents of 569 individuals of Stellifer brasiliensis and Stellifer stellifer from the main channel of the Goiana Estuary were examined to identify variation in the number and the weight of plastic fragments and relate this variation to differences among the seasons (early dry, late dry, early rainy and late rainy), the habitats within the estuary (upper, middle and lower) and the size classes of the fish (juveniles, sub-adults and adults). RESULTS: Plastic fragments were found in 7.9% of the individuals of these two drum species captured from December 2005 to August 2008. Nylon fragments occurred in 9.2% of S. stellifer and 6.9% of S. brasiliensis stomachs. The highest number of nylon fragments ingested was observed in adults during the late rainy season in the middle estuary. DISCUSSION: Blue polyfilament nylon ropes are used extensively in fisheries and can be lost, inappropriately discarded or damaged during use in the estuary. These fragments were the only type of plastic detected during this study. The ingestion of nylon fragments by fish probably occurred during the animals’ normal feeding activities. During the rainy season, the discharge of freshwater transports nylon fragments to the main channel and makes the fragments more available to fish. Fishery activities are responsible for a significant amount of the marine debris found in the estuary. CONCLUSIONS: The ingestion of fragments of nylon threads by fish is a demonstrated form of pollution in the Goiana Estuary. The physiological and toxicological consequences of the ingestion of this type of debris are unknown, as is the actual extent of the problem worldwide. The solutions to the problem are in the hands of authorities and communities alike because the good care and timely replacement of gear requires education, investment and effective policies.