Use of biomarkers in Nile tilapia (Oreochromis niloticus) to assess the impacts of pollution in Bolgoda Lake, an urban water body in Sri Lanka

The present study reports the first analysis of water pollutants in Sri Lankan waters using a suite of biomarkers in Nile tilapia (Oreochromis niloticus) residing in Bolgoda Lake which receives urban, industrial and domestic wastes from multiple sources. The fish were collected from the lake in the dry period (April 2005) and wet periods (September 2005, October 2006) and the levels of biomarkers viz. hepatic ethoxyresorufin O-deethylase (EROD), glutathione S-transferase (GST), metallothioneins, biliary fluorescent aromatic compounds, brain and muscle cholinesterases (ChE) were compared with those of the laboratory reared control fish and the fish obtained from a less polluted water body, Bathalagoda reservoir (reference site). The results revealed that biomarker levels of the fish collected from the reference site were not significantly different from the controls. Hepatic EROD and GST activities in fish from Bolgoda Lake were induced 4.2-16.6 folds and 1.4-3.3 folds respectively compared with the control fish. Analysis of bile in the lake fish revealed recent uptake of naphthalene, pyrene and benzo(a)pyrene type polycyclic aromatic hydrocarbons (PAHs). The induction of EROD activities in feral fish reflects the exposure of fish to aryl hydrocarbon receptor agonists including PAHs present as pollutants in the Bolgoda Lake. Cholinesterase activity in the fish inhabiting one sampling site of Bolgoda Lake was lower (22-40% inhibition) than the activity measured in the control fish indicating the presence of anticholinesterase pollutants in the area. Hepatic metallothionein levels in the lake fish were higher (1.9-3.2 folds) in comparison to the controls indicating metal exposure. The results support the potential use of these biomarkers in Nile tilapia in assessing pollution in tropical water bodies.     

Emission of nitrous oxide from rice-wheat systems of Indo-Gangetic plains of India

Nitrous oxide (N₂O) accounts for 5%of the total enhanced greenhouse effect and responsiblefor the destruction of the stratospheric ozone. The rice-wheat cropping system occupying 26 million ha ofproductive land in Asia could be a major source ofN₂O as most of the fertilizer N in this region isconsumed by this system. Emission of N₂O asinfluenced by application of urea, urea plus farm yardmanure (FYM), and urea plus dicyandiamide (DCD), anitrification inhibitor, was studied in rice-wheatsystems of Indo-Gangetic plains of India. Total emissionof N₂O-N from the rice-wheat systems varied between654 g ha^-1 in unfertilized plots and 1570 g ha^-1 in urea fertilized plots. Application of FYM and DCDreduced emission of N₂O-N in rice. The magnitude ofreduction was higher with DCD. In wheat also N₂O-Nemission was reduced by DCD. FYM applied in rice had noresidual effect on N₂O-N emission in wheat. In riceintermittent wetting and drying condition of soilresulted in higher N₂O-N emission than that ofsaturated soil condition. Treatments with 5 irrigationsgave higher emissions in wheat than those with 3irrigations. In rice-wheat system, typical of a farmer'sfield in Indo-Gangetic plains, where 240 kg N isgenerally applied through urea, N₂O-N emission is1570 g ha^-1 (0.38% of applied N) and application ofFYM and DCD reduced it to 1415 and 1096 g ha^-1,respectively.     

Distribution of Metals in the Edible Plants Grown at Jajmau, Kanpur (India) Receiving Treated Tannery Wastewater: Relation with Physico-Chemical Properties of the Soil

The implications of metal contamination of agricultural soils due to long term irrigation with treated industrial wastewater and their subsequent accumulation in the vegetables/crops growing on such soils has been assessed in an area of industrial complex, Jajmau, Kanpur (India). Physico-chemical properties of the soil were also studied. The soil and vegetables/crops were sampled from an area of 2100 acre agricultural land and analyzed for physico-chemical properties and metal accumulation in different parts of the plants. The comparison of the data of physico-chemical properties of control and contaminated soil showed that salinity, electrical conductivity, available phosphorous, sodium and potassium content (both water soluble and exchangeable) were found high in contaminated soil. The analysis of plant available metal content in the soil showed the highest level of Fe, which ranged from 529.02 to 2615 μg g⁻¹ dw and lowest level of Ni (3.12 to 10.51 μg g⁻¹ dw). The analysis of the results revealed that accumulation of toxic metal Cr in leafy vegetables was found more than fruit bearing vegetables/crops. Thus, it is recommended that the leafy vegetables are unsuitable to grow in such contaminated sites. It is important to note that toxic metal, Ni was not detected in all the plants. The edible part of the vegetables (under ground) such as, garlic (19.27 μg g⁻¹ dw), potato (11.81 μg g⁻¹ dw) and turmeric (20.86 μg g⁻¹ dw) has accumulated lowest level of toxic metal, Cr than leafy and fruit bearing vegetables. In some fruit part of vegetables such as, bitter gourd, egg plant, jack tree, maize and okra, the accumulation of Cr was not detected and may be grown in this area.     

Reduced Metals Concentrations of Water, Sediment and Hyalella Azteca from Lakes in the Vicinity of the Sudbury Metal Smelters, Ontario, Canada

Hyalella azteca (Crustacea: Amphipoda), water and sediments from 12 circum-neutral lakes between Sudbury and North Bay in Ontario, Canada were sampled in August 1998 and analyzed for 10 metals including Cu, Zn, Cd, Ni, Pb, Co, Mo, V, Ba and Ti. Statistical analyses showed that concentrations of the metals in H. azteca, water and sediment differed significantly (ANOVA, P<0.05) among lakes (except for Zn and Pb in H. azteca and Mo in water). There was a trend of declining metal concentration, especially for Cu, Ni and Co (in water, Hyalella and sediment), with distance from the smelters indicating the reduced impact of atmospheric pollution. Metal concentrations of lakes (water) in the Sudbury area were found to be lower compared to data from the 1970s and 1980s indicating an improvement in water quality. Metal concentrations in field-collected amphipods compared favorably with those measured in the laboratory in animals exposed to deep-water sediments, provided metal concentrations were not extremely low (e.g., Pb) and that water chemistry differences (e.g., pH) were taken into account for some metals (especially Cd). In general bioaccumulation of metals in H. azteca was predicted better from surface water than from sediment total metal.     

Carbon isotopic and biochemical fingerprints of sedimentary organic matter in lower Narmada and Tapi rivers,north-west coast of India

Sources of organic matter (OM) in lower Narmada and Tapi river-estuaries were examined using organic carbon to nitrogen ratio (C_org/N), stable carbon isotope ratio (δ¹³C_org) and lignin phenol biomarkers. The signature of lower C_org (av. 0.50%) and higher δ¹³C_org (av. –20.3‰) in Narmada and, higher C_org (av. 0.85%) and lower δ¹³C_org (av. –22.8‰) in Tapi highlight the difference in OM characteristics of both systems, nevertheless they flow adjacent to each other. The OM in Tapi was predominated by fresh plant tissues, as indicated by higher Λ8?=?1.2–3.2?mg/100?mg C_org, lower Ad/Al_v?=?0.22–0.46 and lower LPVI?=?17–23. The plant OM present in the sediments of Narmada was previously degraded and mixed with soil. The OM contribution from algae was restricted to estuarine stations in both the rivers, which was ～50% in Narmada and ～35% in Tapi. The contribution of OM from fresh vascular plant was higher (20% to 63%) in Tapi than Narmada (2% to 35%). This study illustrated the benefits of using lignin phenols along with C_org/N and δ¹³C_org to identify the potential OM sources in two large river–estuary systems of India, which highlighted the complex interaction of natural and anthropogenic processes acted on the terrestrial OM compositions.     

Derivation of motor vehicle tailpipe particle emission factors suitable for modelling urban fleet emissions and air quality assessments

Background, aim and scope  

Urban motor vehicle fleets are a major source of particulate matter pollution, especially of ultrafine particles (diameters < 0.1 μm), and exposure to particulate matter has known serious health effects. A considerable body of literature is available on vehicle particle emission factors derived using a wide range of different measurement methods for different particle sizes, conducted in different parts of the world. Therefore, the choice as to which are the most suitable particle emission factors to use in transport modelling and health impact assessments presented as a very difficult task. The aim of this study was to derive a comprehensive set of tailpipe particle emission factors for different vehicle and road type combinations, covering the full size range of particles emitted, which are suitable for modelling urban fleet emissions.     

Assessment of pollution in road runoff using a Bufo viridis biological assay

Road runoff is a major source of environmental pollution, significantly threatening nearby aquatic habitats. Chemical analyses indicate high pollutant concentrations in the road’s “first flush”, but bioassays are more advantageous for addressing the cumulative effects of the numerous pollutants within the runoff. We used Bufo viridis embryos and larvae to assess the toxicity of road runoff from two major highways in Israel. We show, for the first time, that exposure to midseason runoff not only has an adverse effect on growth and development rates of B. viridis larvae but can also lead to increased rates of morphological deformations. Seasonal first flushes, despite having higher metal concentrations, did not adversely affect the toad larvae, apparently due to a counter effect of organic matter that potentially served as a supplementary energy resource. Road runoff can be a major cause for a qualitative decrease in the quality of aquatic habitats threatening amphibians in Israel.     

Quantifying RDX biodegradation in groundwater using δ15N isotope analysis

Isotope analysis was used to examine the extent of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) biodegradation in groundwater along a ca. 1.35-km contamination plume. Biodegradation was proposed as a natural attenuating remediation method for the contaminated aquifer. By isotope analysis of RDX, the extent of biodegradation was found to reach up to 99.5% of the initial mass at a distance of 1.15–1.35 km down gradient from the contamination sources. A range of first-order biodegradation rates was calculated based on the degradation extents, with average half-life values ranging between 4.4 and 12.8 years for RDX biodegradation in the upper 15 m of the aquifer, assuming purely aerobic biodegradation, and between 10.9 and 31.2 years, assuming purely anaerobic biodegradation. Based on the geochemical data, an aerobic biodegradation pathway was suggested as the dominant attenuation process at the site. The calculated biodegradation rate was correlated with depth, showing decreasing degradation rates in deeper groundwater layers. Exceptionally low first-order kinetic constants were found in a borehole penetrating the bottom of the aquifer, with half life ranging between 85.0 to 161.5 years, assuming purely aerobic biodegradation, and between 207.5 and 394.3 years, assuming purely anaerobic biodegradation.The study showed that stable isotope fractionation analysis is a suitable tool to detect biodegradation of RDX in the environment. Our findings clearly indicated that RDX is naturally biodegraded in the contaminated aquifer. To the best of our knowledge, this is the first reported use of RDX isotope analysis to quantify its biodegradation in contaminated aquifers.