Experimental investigation of groundwater contamination by surface sources: Determination of adsorption capacity,diffusion, and sorption potential of selected anions in different soils

The present study investigated the fate and transport of two significant anions through soil to explore their potential as groundwater contaminants. The retention properties of chloride and sulfate in soils having several significantly different characteristics (soil‐1 and soil‐2) were determined using adsorption test and adsorption‐diffusion column experiments. The maximum adsorption capacity of chloride was 3.7 and 1.16 mg/g, respectively, in soil‐1 and soil‐2, with organic matter (OM) content of 3.92% and 4.69%, respectively. The sulfate adsorption obtained was 24.09% and 13.83%, respectively, in the two soils. The anions exhibited monolayer adsorption in the soils with replacement of hydroxyl ions from soils as the major mechanism of adsorption. On the other hand, the adsorption capacities obtained from the adsorption‐diffusion column experiment were about 100 times lower compared to that of the column tests of both of the soils. The maximum adsorption capacity of chloride was 0.03 mg/g and 0.01 mg/g, respectively, in soil‐1 and soil‐2, whereas that of sulfate was 0.04 mg/g and 0.03 mg/g. The empirical relation for depth of penetration (d) from a known spillage onto the soil surface was determined as a function of sorption capacity (S) and initial anion concentration (C) as d = 0.0073e^(?57S)C and d = 0.0038e^(?35S)C for chloride and sulfate, respectively.     

Size exclusion chromatography for the removal of pigments from extracellular ligninolytic enzyme extracts from decayed wheat straw

Solid-state fermentation of wheat straw was carried out by a native white rot basidiomycete Daedaleopsis flavida strain 5A. Extract prepared from the 12-day decayed wheat straw contained extracellular ligninolytic enzymes like manganese peroxidase (MnP), manganese-independent peroxidase (MIP), lignin peroxidase (LiP) and laccase along with straw-degraded products and pigments. Sephacryl S-200 size exclusion chromatography in 16/100 column was used for the separation of these ligninolytic enzymes and straw-degraded products and pigments. Recovery of pigment-free ligninolytic enzyme activities as protein was 40% of the total proteins loaded and specific LiP activity increased 34 fold after size exclusion chromatography. Thus accurate estimation of LiP by veratryl alcohol oxidation assay was possible only after the removal of interfering pigments. The reproducibility of size exclusion chromatography is adjudged satisfactory from the consistent results obtained after seven repetitive uses of matrices.     

Destruction of cyanide waste solutions using chlorine dioxide,ozone and titania sol

Increasingly, there are severe environmental controls in the mining industry. Because of lack of technological advances, waste management practices are severely limited. Most of the wastes in the milling industrial effluents are known to contain cyanides and it is recognized that after extraction and recovery of precious metals, substantial amounts of cyanide are delivered to tailings ponds. The toxicity of cyanide creates serious environmental problems. In this paper we describe several methods for the treatment of cyanide solutions. These include: (1) cyanide destruction by oxidation with chlorine dioxide (ClO(2)) in a Gas-Sparged Hydrocyclone (GSH) reactor; (2) destruction of cyanide by ozone (O(3)) using a stirred batch reactor, and finally, (3) the photolysis of cyanide with UV light in presence of titania sol. In all cases excellent performance were observed as measured by the extent and of the destruction.     

Role of blue green algae biofertilizer in ameliorating the nitrogen demand and fly-ash stress to the growth and yield of rice (Oryza sativa L.) plants

Rice is a major food crop throughout the world; however, accumulation of toxic metals and metalloids in grains in contaminated environments is a matter of growing concern. Field experiments were conducted to analyze the growth performance, elemental composition (Fe, Si, Zn, Mn, Cu, Ni, Cd and As) and yield of the rice plants (Oryza sativa L. cv. Saryu-52) grown under different doses of fly-ash (FA; applied @ 10 and 100 tha(-1) denoted as FA(10) and FA(100), respectively) mixed with garden soil (GS) in combination with nitrogen fertilizer (NF; applied @ 90 and 120 kg ha(-1) denoted as NF(90) and NF(120), respectively) and blue green algae biofertilizer (BGA; applied @ 12.5 kg ha(-1) denoted as BGA(12.5)). Significant enhancement of growth was observed in the plants growing on amended soils as compared to GS and best response was obtained in amendment of FA(10)+NF(90)+BGA(12.5). Accumulation of Si, Fe, Zn and Mn was higher than Cu, Cd, Ni and As. Arsenic accumulation was detected only in FA(100) and its amendments. Inoculation of BGA(12.5) caused slight reduction in Cd, Ni and As content of plants as compared to NF(120) amendment. The high levels of stress inducible non-protein thiols (NP-SH) and cysteine in FA(100) were decreased by application of NF and BGA indicating stress amelioration. Study suggests integrated use of FA, BGA and NF for improved growth, yield and mineral composition of the rice plants besides reducing the high demand of nitrogen fertilizers.     

Spatial and temporal variations of PM(2.5) concentration and composition throughout an urban area with high freeway density-the Greater Cincinnati study

The PM(2.5) concentration and its elemental composition were measured in the Cincinnati metropolitan area, which is characterized by intense highway traffic. The spatial and temporal variations were investigated for various chemical elements that contributed to the PM(2.5) fraction during a 1-year-long measurement campaign (December 2001-November 2002). The ambient aerosol monitoring was performed in 11 locations around the city during nine measurement cycles. During each cycle, four Harvard-type impactors were operating in parallel in specific locations to explore various factors affecting the PM(2.5) elemental concentrations. The sampling was performed during business days, thus assuring traffic uniformity. The 24-h PM(2.5) samples were collected on Teflon and quartz filters. Teflon filters were analyzed by X-ray fluorescence (XRF) analysis while quartz filters were analyzed by thermal-optical transmittance (TOT) analysis. In addition to PM(2.5) measurements, particle size-selective sampling was performed in two cycles using micro-orifice uniform deposit impactor; the collected fractionated deposits were analyzed by XRF. It was found that PM(2.5) concentration ranged from 6.70 to 48.3 mug m(-3) and had low spatial variation (median coefficient of variation, CV=11.3%). The elemental concentrations demonstrated high spatial variation, with the median CV ranged from 38.2% for Fe to 68.7% for Ni. For traffic-related trace metals, the highest concentration was detected in the city center site, which was close to a major highway. The particle size selective measurement revealed that mass concentration of the trace metals, such as Zn, Pb, Ni, as well as that of sulfur reach their peak values in the particle size range of 0.32-1.0 mum. Meteorological parameters and traffic intensity were not found to have a significant influence on the PM(2.5) elemental concentrations.     

Oxidisability of environmental sulphur under different catalytic conditions

The oxidation of elemental sulphur in the catalytic presence of selected metal ions [Cr(III), Ce(III), Cu(II), Hg(II), Ni(II), Co(II), Mo(VI), Cd(II), Zn(II), Ti(IV), and V(V)], and hydrocarbons (benzene, gasoline, and kerosene) was studied in an alkaline medium buffered by marble powder. The catalytic efficiencies of metal ions were: Cr(III) > Ce(III) > Cu(II) > Hg(II) > Ni(II). The oxidation process was inhibited in the presence of other ions, and the inhibitive effect was in the following order: Co(II) < Mo(VI) < Cd(II) < Zn(II) < Ti(IV) < V(V). In the case of hydrocarbons, the efficiencies were as follows: gasoline > benzene > kerosene. The oxidation of sulphur in sulphur-loaded soils obtained from near a textile mill and a distillery were also carried out in the c both cases was significantly enhanced.To whom all correspondence should be addressed.     

Metals in feathers of sooty tern, white tern, gray-backed tern, and brown noddy from islands in the North Pacific

Levels of heavy metals are usuallyhigher in adult than young birds because they eatlarger, more contaminated prey, or because they havehad longer to accumulate metals in their tissues.Further, levels of contaminants are usually less inbirds nesting on remote, offshore islands than inbirds breeding closer to mainland areas that areurbanized and industrialized. We examined the featherlevels of arsenic, cadmium, chromium, lead, manganese,mercury, and selenium in adult sooty terns (Sterna fuscata), gray-backed terns (Sterna lunata), and brown noddy (Anous stolidus, and adult and young white terns (Gygis alba, fromMidway Atoll, and in adult and young sooty terns andadult brown noddy from Manana Island, Hawaii (chicksof other terns were not available). We tested andrejected the null hypotheses that metal levels are notsignificantly different among species, ages, andlocations. Despite their small size, adult white ternshad the highest levels of lead, arsenic and tin. Brownnoddies had the highest levels of cadmium, chromium,manganese, and selenium. Sooty and white terns had thehighest levels of mercury. Sooty tern adults hadsignificantly higher levels of cadmium, mercury, andselenium than young, while young had significantlyhigher levels of arsenic and manganese. White ternadults had significantly higher levels of selenium andtin than young, while young had higher levels ofcadmium and mercury than adults. Except for mercury,there were significant inter-location differenceswithin species in all heavy metals. Contrary toexpectation, where the differences were great, metalsgenerally were higher in the feathers of terns andnoddies from Midway than from Manana.     

Experimental investigation of solar still with opaque north triangular face

Developing a compact, simple, and productive solar still is a main challenge. This paper describes a simple modification of the solar still that significantly enhances its productivity. A laboratory scale of modified single effect double slope glass solar still with the opaque triangular north wall has been developed and tested for enhancement of productivity in sunny days of the summer season in the month of April. The experiments on still have been carried out under three levels of water depths from 1 to 3 cm and compared it with the performance of conventional still of double slope single effect solar still of the same size. It is clear from the observations that opaque type still gave maximum distillate of 1793 ml at 1 cm depth of water while conventional still could produce only 1519 ml for the same depth of water. Also, for 2 and 3 cm depth of water, the opaque type still found to be more productive than conventional double slope solar still. As the former produced 1532 and 1464 ml while the latter produced 1328 and 1235 ml, for 2 and 3 cm depth of water, respectively.     

Changing lichen diversity in and around urban settlements of Garhwal Himalayas due to increasing anthropogenic activities

Decrease in lichen diversity is an important biometric tool to assess the prevailing environmental condition in an area. An attempt has been made to explore the utility of lichen diversity in the monitoring of air pollution in the city of Pauri and Srinagar, Garhwal Himalayas, Uttaranchal. Eighty five lichen species were recorded from Pauri and Srinagar (Garhwal) in June 2005. It was observed that polluted sites had very low lichen diversity, mostly dominated by members of lichen family Physciaceae. Kiyonkaleshwar area is the site with maximum lichen diversity (46 lichen taxa) located in a more or less pollution-free area of Pauri city. Two-dimensional principal components analysis plot revealed significant positive contribution of natural (unaltered) sites towards lichen biodiversity, thus affirming the utility of lichen diversity in biomonitoring studies in a wide geographical area.     

Hydrogeochemistry for the assessment of groundwater quality in Varanasi: a fast-urbanizing center in Uttar Pradesh, India

The hydrogeochemical parameters for groundwater samples of the Varanasi area, a fast-urbanizing region in India, were studied to evaluate the major ion chemistry, weathering and solute acquisition processes controlling water composition, and suitability of water quality for domestic and irrigation uses. Sixty-eight groundwater samples were collected randomly from dug wells and hand pumps in the urban Varanasi area and analyzed for various chemical parameters. Geologically, the study area comprises Quaternary alluvium made up of an alternating succession of clay, silty clay, and sand deposits. The Total dissolved solids classification reveals that except two locations, the groundwater samples are desirable for drinking, and all are useful for irrigation purposes. The cationic and anionic concentrations indicated that the majority of the groundwater samples belong to the order of Na > Ca > Mg > K and HCO₃ > Cl > SO₄ types, respectively. Geochemical classification of groundwater based on the Chadha rectangular diagram shows that the majority (81%) of groundwater samples belong to the calcium?Cbicarbonate type. The HCO₃/ (HCO₃ + SO₄) ratio (0.87) indicates mostly carbonic acid weathering process due to presence of kankar carbonate mixed with clay/fine sand. The high nitrate concentration (>45?mg/l) of about 18% of the groundwater samples may be due to the local domestic sewage, leakage of septic tanks, and improper management of sanitary landfills. In general, the calculated values of sodium adsorption ratio, percent sodium, residual sodium carbonate, and permeability index indicate good to permissible use of water for irrigation, and only a few locations demand remedial measures for better crop yields.