Uptake and Dupuration of Petroleum Hydrocarbons By the Backwater Clam,Meretrix Casta Chemnitz

Meretrix casta were experimentally exposed to water soluble fractions of refined and crude oil and their rate of accumulation of the petroleum hydrocarbons including total and individual aromatics viz., naphthalene, methylnaphthalene and dimethylnaphthalene, was studied. Subsequent transfer to clean waters in the laboratory and field resulted in depuration of the accumulated hydrocarbons from tissues. in general, the rate of discharge was found to be dependent on the concentration that the animals had been earlier exposed to and also the alkylation of aromatic hydrocarbons. Occasional increases were observed in the hydrocarbon values of clams which were placed in the field, compared to their laboratory counterparts, suggesting an intermittent source of petroleum hydrocarbon input into the environment. the influence on the rate of uptake, release and retention of hydrocarbons in the clams is discussed.     

Biosorption of hexavalent chromium and malachite green from aqueous effluents,using Cladophora sp.

Biosorption potential of green macroalgae Cladophora sp., (GAC) for the removal of hexavalent chromium (Cr(VI)) and malachite green (MG) from aqueous medium was investigated. Optimal conditions for biosorption experiments were determined as a function of initial pH, GAC dosage, temperature and initial concentration of Cr(VI) and MG. The biosorption equilibrium data were fitted with the isotherm models of Langmuir, Freundlich, Kiselev, Frumkin and Jovanovic, while the experimental data were analysed using the kinetic models such as pseudo-first-order, pseudo-second-order, Ritchie's and intraparticle diffusion. The Langmuir maximum biosorption capacity was calculated as 100.00?mg/g (Cr(VI)) and 142.85?mg/g (MG). The biosorption kinetic data showed better agreement with the pseudo-second-order kinetic model. The thermodynamic parameters indicated spontaneous and endothermic nature of the biosorption process for Cr(VI) removal, whereas exothermic in the case of MG removal. Furthermore, the biosorption efficiencies of the GAC reusability were found significant up to five cycles and tested using 0.1, 0.5 and 1.0?M HCl, respectively. The results of the present study indicated that GAC is a suitable biosorbent for the sequestration of Cr(VI) and MG from aqueous solutions.     

Plasmid mediated antibiotic resistance in marine bacteria

This research work was conducted in Uppanar estuary to ascertain the role of plasmids in the antibiotic resistance of bacteria. Water and sediment samples were collected for a period of three months. When tested against 20 antibiotics 22 MAR strains were isolated from the samples, which were found resistant to 5-13 antibiotics. They belong to 7 genera and 10 species. Gram-negative bacteria namely Neisseria mucosa, N. sicca, Branhamella catarrhalis, Klebsiella ozaenae, Citrobacterintermedius, Pseudomonas fluorescens and Enterobacter aerogenes were isolated. Gram-positive bacteria were of Bacillus subtilis, B. megaterium and Micrococcus luteus. When plasmid curing was done using acredine orange, the resistance against penicillin-G, ampicillin, tetracycline, amoxycillin, kanamycin, and chloramphenicol were totally lost in all strains, which confirmed the role of plasmid in these strains against antibiotics. Ten strains belong to different species were selected for the plasmid isolation and electrophoresis was done. Presence of plasmids in all strains was confirmed and the molecular weight was in the range of 2850 to 3170 bp. The study revealed that MAR strains are common in Uppanar estuary and they are plasmid mediated. This environment is seemed to be deteriorating at an alarming rate.     

Lab-on-a-chip technologies for food safety,processing, and packaging applications: a review

Environmental Chemistry Letters - The advent of microfluidic systems has led to significant developments in lab-on-a-chip devices integrating several functions onto a single platform. Over the...     

Ammonia in the atmosphere: a review on emission sources, atmospheric chemistry and deposition on terrestrial bodies

Gaseous ammonia (NH₃) is the most abundant alkaline gas in the atmosphere. In addition, it is a major component of total reactive nitrogen. The largest source of NH₃ emissions is agriculture, including animal husbandry and NH₃-based fertilizer applications. Other sources of NH₃ include industrial processes, vehicular emissions and volatilization from soils and oceans. Recent studies have indicated that NH₃ emissions have been increasing over the last few decades on a global scale. This is a concern because NH₃ plays a significant role in the formation of atmospheric particulate matter, visibility degradation and atmospheric deposition of nitrogen to sensitive ecosystems. Thus, the increase in NH₃ emissions negatively influences environmental and public health as well as climate change. For these reasons, it is important to have a clear understanding of the sources, deposition and atmospheric behaviour of NH₃. Over the last two decades, a number of research papers have addressed pertinent issues related to NH₃ emissions into the atmosphere at global, regional and local scales. This review article integrates the knowledge available on atmospheric NH₃ from the literature in a systematic manner, describes the environmental implications of unabated NH₃ emissions and provides a scientific basis for developing effective control strategies for NH₃.     

A comparative evaluation of passive and active samplers for measurements of gaseous semi-volatile organic compounds in the tropical atmosphere

The polyurethane foam (PUF) disk-based passive air samplers (PAS), mounted inside two aluminium bowls to buffer the air flow to the disk and to shield it from precipitation and sunlight, were used for the collection of atmospheric SVOCs in Singapore during April 2008–June 2008. Data obtained from PAS measurements are compared to those from active high-volume air sampling (AAS). Single factor ANOVA tests show that there were no significant differences in chemical distribution profiles between actively and passively collected samples (PAHs, F = 3.38 × 10^?8 < F_critical = 4.17 with p > 0.05; OCPs, F = 2.71 × 10^?8 < F_critical = 4.75 with p > 0.05). The average air-side mass transfer coefficient (k_A) for PAS, determined from the loss of depuration compounds such as 13C₆ – HCB (1000 ng), 13C₁₂ – 4,4′ DDT (1000 ng) and 13C₁₂ – PCB 101 (1000 ng)spiked on the disks prior to deployment, was 0.12 ± 0.04 m s^?1. These values are comparable to those reported previously in the literature. The average sampling rate was 3.78 ± 1.83 m³ d^?1 for the 365 cm² PUF disk. Throughout the entire sampling period (～68 d), most of the PAHs and all OCPs exhibited a linear uptake trend on PAS, while naphthalene, acenaphthylene, acenaphthene and fluorene reached the curvilinear phase after the first ～30 d exposure. Theoretically estimated times to equilibrium (t_eq) ranged from around one month for Acy to hundreds of years for DB(ah)A. Sampling rates, based on the time integrated active sampling-derived concentrations and masses collected by PUF disks during the linear uptake phase, were determined for all target compounds with the average values of 2.50 m³ d^?1 and 3.43 m³ d^?1 for PAHs and OCPs, respectively. More variations were observed as compared to those from the depuration study. These variation were most likely due to the difference of physicochemical properties of individual species. Lastly, multiple linear regression models were developed to estimate the log-transformed gaseous concentration of an individual compound in air based on the mass collection rate of the gaseous SVOCs measured using the PAS and the molecular weight (MW) of the particular compound for both PAHs and OCPs, respectively.     

Sublethal effect of silver and chromium in the green mussel Perna viridis with reference to alterations in oxygen uptake, filtration rate and membrane bound ATPase system as biomarkers

Perna viridis is an ideal animal for studying the impairment caused by the effects of heavy metals that are often detected in coastal areas. Preliminary bioassay tests revealed that the lethal (LC(100)), median lethal (LC(50)) and sublethal (LC(0)) concentration of silver and chromium to P. viridis were 6.5, 4.0, 2.0 mg l(-1) and 4.5, 2.5, 1.0 mg l(-1), respectively. Toxic effect of silver and chromium was evaluated in the green mussel P. viridis, with reference to oxygen consumption, filtration rate and ATPase system in laboratory experiments. These parameters were selected as the end point of sublethal stress. Oxygen consumption and filtration rates were calculated as a measure of decline in the dissolved oxygen level and algal concentration (feed) in the aquaria water, respectively. Silver and chromium affects both oxygen consumption and filtration rate significantly (P<0.01) at 96 h when compared to control. The activity of ATPases system in the gills, hepatopancreas, ovary and muscle of mussels were inhibited by silver and chromium indicating that metals exerted significant toxic effect. The inhibition of Na(+)K(+) ATPase, Ca(2+) ATPase and Mg(2+) ATPase in the mussels were significant (P<0.05) for silver and highly significant (P<0.01) for chromium, which indicates that chromium was more toxic to mussels when compared to silver. The assessment of oxygen consumption, filtration and ATPases system can thus be used as a valid biomarker in aquatic ecotoxicology studies.     

Weather integrated malaria prediction system using Bayesian structural time series model for northeast states of India

Environmental Science and Pollution Research - Malaria is an endemic disease in India and targeted to eliminate by the year 2030. The present study is aimed at understanding the epidemiological...