Characterization and Identification of the Sources of Chromium, Zinc, Lead, Cadmium, Nickel, Manganese and Iron in Pm10 Particulates at the Two Sites of Kolkata, India

Monitoring of ambient PM₁₀ (particulate matter which passes through a size selective impactor inlet with a 50% efficiency cut-off at 10 μm aerodynamic diameter) has been done at residential (Kasba) and industrial (Cossipore) sites of an urban region of Kolkata during November 2003 to November 2004. These sites were selected depending on the dominant anthropogenic activities. Metal constituents of atmospheric PM₁₀ deposited on glass fibre filter paper were estimated using Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES). Chromium (Cr), zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), manganese (Mn) and iron (Fe) are the seven toxic trace metals quantified from the measured PM₁₀ concentrations. The 24 h average concentrations of Cr, Zn, Pb, Cd, Ni, Mn and Fe from ninety PM₁₀ particulate samples of Kolkata were found to be 6.9, 506.1, 79.1, 3.3, 7.4, 2.4 and 103.6 ng/m³, respectively. The 24 h average PM₁₀ concentration exceeded national ambient air quality standard (NAAQS) as specified by central pollution control board, India at both residential (Kasba) and industrial (Cossipore) areas with mean concentration of 140.1 and 196.6 μg/m³, respectively. A simultaneous meteorology study was performed to assess the influence of air masses by wind speed, wind direction, rainfall, relative humidity and temperature. The measured toxic trace metals generally showed inverse relationship with wind speed, relative humidity and temperature. Factor analysis, a receptor modeling technique has been used for identification of the possible sources contributing to the PM₁₀. Varimax rotated factor analysis identified four possible sources of measured trace metals comprising solid waste dumping, vehicular traffic with the influence of road dust, road dust and soil dust at residential site (Kasba), while vehicular traffic with the influence of soil dust, road dust, galvanizing and electroplating industry, and tanning industry at industrial site (Cossipore).     

Seasonal variations in species composition,abundance, biomass and production rate of tintinnids (Ciliata: Protozoa) along the Hooghly (Ganges) River Estuary,India: a multivariate approach

The study is the first documentation of seasonal variations in species composition, abundance and diversity of tintinnid (Ciliata: Protozoa), in relation to water quality parameters along the stretch of the Hooghly (Ganges) River Estuary (HRE), eastern coastal part of India. A total of 26 species (22 agglomerated and 4 non-agglomerated) belonging to 8 genera has been identified from 8 study sites where Tintinnopsis (17 species) represented the most dominant genera, contributing up to 65 % of total tintinnid community followed by Tintinnidium (2 species), Leprotintinnus (2 species) and Dadayiella, Favella, Metacylis, Eutintinnus and Helicostomella (each with solitary species). The maximum (1,666 ind.?l^?1) and minimum (62 ind.?l^?1) abundance of tintinnids was recorded during post-monsoon and monsoon, respectively. A distinct seasonal dynamics in terms of biomass (0.005–2.465 μg C l^?1) and daily production rate (0.04–3.13 μg C l^?1 day^?1) was also noticed, accounting highest value during pre-monsoon. Chlorophyll a and nitrate were found to be potential causative factors for the seasonal variations of tintinnids as revealed by a stepwise multiple regression model. The result of ANOVA showed a significant variation between species abundance and months (F?=?2.36, P?≤?0.05). k-dominance curves were plotted to determine the comparison of tintinnid dominance between the investigated stations. Based on a principal component analysis (PCA), three main groups were delineated with tintinnid ciliates and environmental parameters. The changes in lorica morphology in terms of temperature and salinity, recorded for three dominant species, provided information on the ecological characteristics of the species assemblage in this estuarine system.     

Trace elements in surface sediments of the Hooghly (Ganges) estuary: distribution and contamination risk assessment

Our objective was to evaluate distribution and accumulation of trace elements (TEs) in surface sediments along the Hooghly (Ganges) River Estuary, India, and to assess the potential risk with view to human health. The TE concentrations (mg kg^?1 dry weight) exhibited a wide range in the following order: Al (31.801 ± 15.943) > Fe (23.337 ± 7584) > Mn (461 ± 147) > S (381 ± 235) > Zn (54 ± 18) > V (43 ± 14) > Cr (39 ± 15) > As (34 ± 15) > Cu (27 ± 11) > Ni (24 ± 9) > Se (17 ± 8) > Co (11 ± 3) > Mo (10 ± 2) > Hg (0.02 ± 0.01). Clay, silt, iron, manganese and sulphur were important for the accumulation of TE in the sediments as confirmed by factor analysis and Pearson correlation. The accumulation and dispersal of TEs were most likely to be governed by both tide-induced processes and anthropogenic inputs from point and non-point sources. Enrichment factor analysis and geoaccumulation index revealed serious contamination of the sediments with Se and As, while comparing the consensus-based sediment quality guidelines (SQGs), adverse biological effects to benthic fauna might be caused by As, Cu, Ni and Cr. This investigation may serve as a model study and recommends continuous monitoring of As, Se, Cu, Ni and Cr to ascertain that SQGs with respect to acceptable levels of TEs to safeguard geochemical health and ecology in the vicinity of this estuary.     

Bioaccumulation of heavy metals in fish tissues of a freshwater lake of Bhopal

Contamination of heavy metals, namely, lead, cadmium, zinc, nickel, copper, chromium and mercury was evaluated in the samples of water and tissues of Labeo rohita and Ctenopharyngodon idella of Upper Lake of Bhopal collected during summer, rainy and winter seasons of 2005–2006. Different organs of the fishes accumulated varying quantities of different heavy metals. In L. rohita, accumulation of heavy metals was in the sequence liver > kidney > gills > muscles, and in C. idella, it was gills > liver > kidney > muscles. Zn was the highest accumulating metal in fish, whilst Hg was the lowest and was well corroborated with those of water. The values of heavy metals were so far well within the maximum permissible standard value of heavy metals for drinking water and for fish culture as prescribed by various national and international agencies.     

Cross-reactivity of anti-Salmonella egg-yolk antibodies to Salmonella serovars

The cross-reactivity of egg yolk antibodies specific to antigens of Salmonella Enteritidis and Salmonella Typhimurium to killed bacterial cells of common Salmonella serovars were tested using an indirect Enzyme Linked Immunosorbent Assay (ELISA). Egg yolk antibodies were produced against purified fimbriae, flagella and lipopolysaccharide (LPS) of S. Enteritidis strain ATCC13076 and flagella, LPS and outer membrane proteins (OMP) of S. Typhimurium strain ATCC13311. For immunological specificity of egg yolk antibodies against killed bacterial cells, we found that the titers of the anti-S. Enteritidis egg yolk antibodies were higher than those of the anti-S. Typhimurium antibodies. In the evaluation of cross-reactivity of these egg yolk antibodies to various Salmonella serovars, we observed that the anti-S. Enteritidis antibodies exhibited more specific affinity than those of the anti-S. Typhimurium antibodies. All S. Enteritidis strains reacted specifically with the anti-S. Enteritidis fimbrial and flagellar egg yolk antibody whereas anti-S. Enteritidis LPS and anti-S. Typhimurium LPS, OMP and flagellar antibodies displayed non-specific reactivity to all Salmonella serovars used in this study. This finding suggests that it may be possible to design a anti-fimbrial egg yolk antibody of S. Enteritidis as a diagnostic tool and a cocktail of OMP and LPS antigens of S. Enteritidis and S. Typhimurium could be used for administering broad spectrum passive immunity to protect against the colonization of pathogenic Salmonella strains in food animals.     

Quantification of ionophores in aged poultry litter using liquid chromatography tandem mass spectrometry

Veterinary anticoccidials, biochemically known as ionophores, are widely used in poultry feed at therapeutic levels to treat Coccidiosis and at sub-therapeutic levels for growth- promotion. Commonly used ionophores in the US poultry industry are monensin, salinomycin, lasalocid and narasin. There is an increasing concern regarding the persistence of these anticoccidials in the environment. However, little attention has been directed to methods development for quantitatively measuring ionophores in complex environmental matrices such as poultry litters that are land applied. Here, we describe a rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS)-based method developed for simultaneous quantification of monensin, lasalocid, salinomycin, and narasin in aged poultry litter samples. Results show significant level of monensin (97.8 ± 3.2?μg kg(-1)), lasalocid (19.2 ± 6.6?μg kg(-1)), salinomycin (70 ± 2.7?μg kg(-1)) and narasin (57.3 ± 2.6?μg kg(-1)) in poultry litter stored for over three years at < 5°C. Our findings indicate that even after several years of unmanaged storage of poultry litter, ionophores may continue to persist in this matrix, raising the possibility of prolonged release into the environment.     

Preparation of Economically Viable and Environment Friendly Composites from Effluents of Aleuritic Acid Industry

The synthesis of aleuritic acid from shellac is associated with generation of huge quantity of waste whose disposal leads to clogging of the sewage system and contaminates the water bodies into which the drain leads. The shellac waste, which was collected from the factory site and Jute fiber has been used to form a sustainable, eco-efficient and economical composite. Characterization of the resin and composite was done by FTIR, TG, DSC and SEM. Mechanical properties of the composites like tensile strength and impact strength etc. were measured.     

Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase

A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT). The effect of pH was examined in the reduction step: at pH 6 the reaction occurred much more rapidly than at pH 8. In the second step, optimal pH and substrate ratio, minimal enzyme concentration and effect of polyethylene glycol (PEG) as an additive for greater than 95% conversion of DAT, over a 3h reaction period were determined using high performance liquid chromatography. Two enzymes were investigated and compared: Arthromyces ramosus peroxidase (ARP) and soybean peroxidase (SBP). The optimal pH values were 5.4 and 5.2 for ARP and SBP, respectively, but SBP was more resistant to mild acid whereas ARP was more stable in neutral solutions. SBP was found to have a greater hydrogen peroxide demand (optimal peroxide/DAT molar ratio for SBP: 2.0 and 3.0 for 2,4-diaminotoluene (2,4-DAT) and 2,6-diaminotoluene (2,6-DAT), respectively; for ARP: 1.5 and 2.75 for 2,4-DAT and 2,6-DAT, respectively) but required significantly less enzyme (0.01 and 0.1 U ml(-1) for 2,4-DAT and 2,6-DAT, respectively) to convert the DAT than ARP (0.4 and 1.5 U ml(-1) for 2,4-DAT and 2,6-DAT, respectively). PEG was shown to have no effect upon the degree of substrate conversion for either enzyme.