Environmental monitoring of carbaryl applied in urban areas to control the glassy-winged sharpshooter in California

Carbaryl insecticide was applied by ground spray to plants in urban areas to control a serious insect pest the glassy-winged sharpshooter, Homalodisca coagulata (Say), newly introduced inCalifornia. To assure there are no adverse impacts to human health and the environment from the carbaryl applications, carbaryl was monitored in tank mixtures, air, surface water, foliage and backyard fruits and vegetables.Results from the five urban areas – Porterville, Fresno, Rancho Cordova, Brentwood and Chico – showed there were no significanthuman exposures or impacts on the environment. Spray tank concentrations ranged from 0.1–0.32%. Carbaryl concentrationsin air ranged from none detected to 1.12 g m^-3, well below the interim health screening level in air of 51.7 g m^-3. There were three detections of carbaryl in surface water nearapplication sites: 0.125 ppb (parts per billion) from a water treatment basin; 6.94 ppb from a gold fish pond; and 1737 ppbin a rain runoff sample collected from a drain adjacent to a sprayed site. The foliar dislodgeable residues ranged from 1.54–7.12 g cm^-2, comparable to levels reported forsafe reentry of 2.4 to 5.6 g cm^-2 for citrus. Carbarylconcentrations in fruits and vegetables ranged from no detectableamounts to 7.56 ppm, which were below the U.S.EPA tolerance, allowable residue of 10 ppm.     

Formation and Emission of N2O and CH4 from Compost Heaps of Organic Household Waster

Composting can be a source of N₂O andCH₄ production. In this investigation, differentcompost heaps of organic household waste weremonitored with the focus on potential formation ofCH₄ and N₂O in the heaps and emission ofthese gases from the heaps. The studied compost heapshad different compost ages, turning intervals andcompost sizes. The analysed compost gases containedbetween 1–3421 L of N₂O-N L^-1 and 0–470 mL of CH₄ L^-1. The emission rates ofN₂O and CH₄ from the compost heaps werebetween 1–1464 mg N₂O m^-2 day^-1 and0–119 000 mg CH₄ m^-2 day^-1. These verylarge differences in compost gas composition andemission indicate the importance of compostmanagement. The results also give an understanding ofwhere in the composting process an increasing emissionof N₂O and CH₄ can occur.     

Atrazine and Alachlor Inputs to Surface and Ground Waters in Irrigated Corn Cultivation Areas of Castilla-Leon Region, Spain

The inputs of atrazine and alachlor herbicides to surface and ground waters from irrigated areas dedicated to corn cultivation in the Castilla-León (C-L) region (Spain) as related to the application of both herbicides were studied. Enzyme-linked immunosorbent assays (ELISA) were used for monitoring the atrazine and alachlor concentrations in 98 water samples taken from these areas. Seventy-nine of the samples were of ground waters and 19 were of surface waters. The concentration ranges of the herbicides detected in the study period (October 1997–October 1998) were 0.04–25.3 g L^–1 in the surface waters and 0.04–3.45 g L^–1 in the ground waters for atrazine, and 0.06–31.9 g L^–1 in the surface waters and 0.05–4.85 g L^–1 in the ground waters in the case of alachlor. The highly significant correlation observed between the concentrations of both herbicides in the surface waters (r = 0.89, p < 0.001) pointed to a parallel transport of atrazine and alachlor to these waters. A study was made of the temporal evolution of the concentrations of both herbicides, and it was found a maximum recharge of atrazine in the ground waters for April 1998 and of alachlor in October 1997 and October 1998. The temporal evolution of the concentrations of both herbicides in surface waters was parallel. The highly significant correlations observed between atrazine concentrations determined by ELISA and by HPLC (r = 0.92, p < 0.001) and between alachlor concentrations also determined by both methods (r = 0.96, p < 0.001) confirmed the usefulness of ELISA for monitoring both herbicides in an elevated number of samples. Using HPLC, the presence in some waters of the alachlor ethanesulfonate (ESA) metabolite was found at a concentration range of 0.52–4.01 g L^–1. However the interference of ESA in the determination of alachlor by ELISA was negligible. The inputs of atrazine and alachlor to waters found in this study, especially the inputs to ground waters, could pose a risk for human health considering that some waters, though sporadically, are even used for human consumption.     

Distribution of heavy metals in plants and fish of the Yamuna river (India)

The distribution of cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), manganese (Mn), nickel (Ni), lead (Pb) and zinc (Zn) in the plants and fish of Yamuna river from Delhi to Allahabad, a distance of about 840 km, at five sampling stations was determined in the year 1981. The results have shown wide variations in the heavy metal levels from one sampling station to the other. The concentrations of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn in the plants (Eicchornia crassipes) were found to be 0.02–0.12, 2.7–21.3, 4.6–64.8, 9.8–114.0, 193.0–1835.0, 380.0–1443.0, 4.4–83.0, 4.8–30.2, and 22.1–356.5 g g^-1 respectively whereas in the fish (Heteropnuestes fossilis) were found to be ND-0.40, 2.3–13.7, 3.7–26.9, 8.33–58.1, 278.3–1108.0, 81.3–213.8, 2.8–32.7, 1.4–12.8 and 101.8–364.8 gg^-1 respectively on dry weight basis.     

Concentrations of Cadmium, Mercury and Selenium in Blood, Liver and Kidney of Common Eider Ducks from the Canadian Arctic

We determined concentrations of selected trace elements inlivers, kidneys and blood samples from common eiders (Somateria mollissima borealis) from the eastern Canadianarctic during 1997 and 1998. Concentrations of totalmercury and organic mercury were generally low in the liversof these birds (less than 6 and 4 g g^–1 dry wt,respectively). Selenium ranged between 11–47 g g^–1 inlivers. Renal cadmium concentrations were among the highestever published for this species (range: 47–281 g g^–1). The regressions of log-transformed concentrations ofthese trace elements in blood samples on those in liver orkidney were significant (all P-values < 0.05) andpositive. However, except for organic mercury (RM ² = 0.83), the co-efficients of determination were low tomoderate (range of R ²: 0.26–0.52), suggesting poorto moderate predictive capability. Furthermore, therelationships between total mercury in blood and liverchanged between 1997 and 1998, suggesting that it would notbe possible to predict consistently, concentrations ofmercury in blood from those in liver based on samples takenin one year. Blood samples can be used to determineconcentrations of these trace elements in common eiders (andprobably other sea duck species as well). The use of bloodsamples is especially warranted when it is undesirable tokill the animal such as when working with rare or endangeredsea duck species or when the objective is to relate traceelement exposure to annual survival rates. However, thepredictive equations developed here should not be used topredict expected concentrations in one type of tissue fromthose in the other.     

Nitrogen isotope ratios in pine bark as an indicator of N emissions from anthropogenic sources

The article describes the use of Scots pine bark to identifynitrogen sources in eastern Germany, as well as background areas in Russia and Bulgaria, by using natural isotope ratios of total nitrogen (N_t) and individual N compoundssuch as ammonium (NH₄ ⁺), nitrate (NO₃ ^-)and amid nitrogen (amide-N). The samples collected were analysed using an elemental analyser in connection with a gas isotope mass spectrometer (EA-IRMS). Natural ¹⁵N abundances in pine bark from impact areas suggest that the ammonium accumulated on the surface of the bark is releasedfrom livestock management. Bark of Scots pines growing near agricultural land had highly depleted ¹⁵N_t values (between –8 and –12), while bark from background areas (unpolluted areas) displayed slightly negative ¹⁵N_t values (mean ¹⁵N_t = –3.8). It is assumed that part of the N adsorbed on the bark surface is mainly derived from ammonia(mean ¹⁵N_t = –40.3) escaping from livestock housing and during the application of manure. This assumption is confirmed by experiments under controlled conditions in which manure samples were spread on soil. In addition, temporal and spatial variations of ¹⁵N_t abundances in pine bark from various locations in eastern Germany as wellas pine stands in Nature Park Dübener Heath are discussed.     

A Survey of Trace Metals in Vegetation, Soil and Lower Animal Along Some Selected Major Roads in Metropolitan City of Lagos

The concentration of trace metals (Cd, Cu, Pb and Zn) in a total of 144 samples of grass, soil and lower animal (earthworm, Lybrodrilus violaceous) were collected and analysed for their metallic content. Levels of cadmium ranged from 0.01–0.07 g g^–1; 0.01–0.12 g g^–1 and from trace–0.05 g g^–1 dry weight for plant, soil and animal samples respectively. Mean concentration of copper ranged 0.10–1.48 g g^–1; 0.10–2.90 g g^–1 and 0.01–0.08 g g^–1 for samples in similar order as above. The levels of Pb varied from 0.01–0.14 g g^–1; 0.02–0.23 g g^–1 and from trace–0.07 g g^–1 while that of Zn ranged from 0.19–1.80 g g^–1; 0.51–3.35 g g^–1and 0.01–0.08 g g^–1 also in the same order of samples as mentioned above. Levels of metals in soil samples were higher than the background levels with the exception of Zn but lower than European Union (EU) limits. The results generally revealed the presence of metals in plant and animal samples and metal dynamics up the food chain is highly possible. Acceptable recoveries of the spiking experiment validate the experimental protocol.     

Organochlorines and selenium in California night-heron and egret eggs

Exceptionally high concentrations of DDE were found in black-crowned night-heron (Nycticorax nycticorax) (geometric mean 8.62 g g^–1 wet wt.) and great egret (Casmerodius albus) (24.0 g g^–1) eggs collected from the Imperial Valley (Salton Sea), California in 1985. DDE concentrations in 14 of the 87 (16%) randomly selected night-heron eggs from six colonies (two in San Francisco Bay, three in the San Joaquin Valley, and one at Salton Sea) were higher than those associated with reduced reproductive success of night-herons (8 g g^–1). In addition, mean shell thickness of night-heron eggs collected from the San Joaquin Valley and from San Francisco Bay during 1982–1984 was significantly less than pre-DDT thickness and was negatively correlated (r=–0.50, n=75, P<0.0001) with DDE concentration. Mean selenium concentration in night-heron eggs from Salton Sea (1.10 g g^–1) was significantly higher than in eggs from three locations in the San Joaquin Valley, and in egret eggs from Salton Sea.     

Pesticide Contamination of Jamaican Environment. II. Insecticide Residues in the Rivers and Shrimps of Rio Cobre Basin, 1982–1996

Only organochlorine (OC) residues were monitored by gas chromatographyin water, sediment and shrimp samples collected everymonth between July 1982 and August 1983 from therivers of Rio Cobre basin. In samples collected everyfour months during 1989–1990, and seven times duringJuly 1995–March 1996, OC and OP (organophosphates)residues were monitored. Carbamate and pyrethroidresidues were not monitored. The detection ofresidues in 1982–1983 was 54 to 100% in water andsediment, and 83 to 100% in shrimp samples fromvarious sampling stations in the four rivers. In otheryears, it ranged from about 40 to 100% in the threetypes of samples.In 1982–1983, DDE and dieldrin residues were found tobe much higher than those of lindane and - and-endosulfan in Black River, Rio Pedro, ThomasRiver and Rio Cobre in the watershed. The ranges ofmeans of each residue in water (g L^-1), sediment(ng g^-1) and shrimp (ng g^-1) samples, respectively, were:DDE, 0.059–102.0, 3.44–13.97, 0.344–14.57;dieldrin, 0.026–173.6, 1.21–2.75, 0.427–5.59;-endosulfan, bdl, 1.75–4.00, bdl;-endosulfan, bdl (below detectable limits), 2.51–9.48, bdl;and lindane, (bdl), 0.110–0.319, 2.90.In 1989–1990 and 1995–1996, residues of six OCs and two OPs were detected quite regularly. DDE, dieldrinand Chlorpyrifos residues were much higher than thoseof the other insecticides. The range of their meansin water (g L^-1), sediment and shrimp (ng g^-1),respectively, were: DDE, 1.66–19.76, 0.941–5.84,1.11–8.32; dieldrin, 0.077–7.22, 0.425–3.31,0.385–1.59; -endosulfan, 0.034–1.25, 0.021–1.22, 0.032–3.62; -endosulfan, 0.665–1.23,0.008–3.60, 0.005–3.97; endosulfan sulphate, 0.959–1.34, 0.035–3.08, 0.012–1.80; lindane, bdl,0.005–0.82, 1.19–1.56; chlorpyrifos, 0.702–4.06,0.005–1.51, 0.156–7.04; and diazinon, bdl, 0–0.150, 0.001–0.006. At the mouth of the river, whereit discharges into the sea, the levels of almost allthe residues were higher than upstream.     

Behaviour and fluxes of trace and toxic elements in creek sediment near Mumbai,India

Studies on marine sediments are extremely important since they act as ultimate sink of anthropogenic pollutants. The present study was conducted near Mumbai city of India to understand andassess the behaviour and fluxes of trace and toxic elements increek sediment. Seven sediment core samples were collected andanalysed for trace and toxic elements such as Fe, Cu, Pb, Zn, Rb and Sr in different sections of the core using EDXRF technique. The fluxes of the elements in each section of the core were calculated using the mass sedimentation rates derivedfrom ²¹⁰Pb dating technique and the sediment density at each location. The estimated depositional fluxes of Fe, Rb and Sr in Zone-1 and Zone-3 are in the ranges of 0.4–0.5% cm^-2yr^-1; 4–6 g cm^-2 yr^-1 and 10–20 g cm^-2 yr^-1 respectively, where as they were about 3–4 times higher in zone-2 for the same elements. The depositionalfluxes of elements Cu (40–60 g cm^-2 yr^-1), Zn (35–43 g cm^-2 yr^-1) and Pb (6–12 g cm^-2 yr^-1) were also found to be higher in zone-2 compared tozone-1 and zone-3 which can be attributed to the release from thenewly developed chemical zone of Thane-Belapur industrial belt.     

Regional monitoring of lead and cadmium contamination in a tropical grazing land site,Thailand

An investigation was carried out to monitor Pb and Cd contamination in grazing land located near a highway. Environmental media at different distances fromhighway (soil, grass, water, cow's forage, fertilizer,manure and milk samples) were collected from three samplinglocations. Soil and grass were characterized by high metalmobility (soil with Pb: 5.25±0.71–14.59±1.17 mgkg^-1, dry mass and Cd: 0.038–0.33±0.04 mg kg^-1, dry mass and grass with Pb: 0.76±0.05–6.62±0.18 mg kg^-1, dry mass and Cd: 0.17±0.01–0.73±0.09 mg kg^-1, dry mass). One-way analysis of variane (ANOVA) was applied to find out the correlation between metal (total and bioavailable) concentrationsin the soil and the distance from roadside. In most cases, the finding showed that plants growing nearer to the highway are usually exposed to more heavy metal accumulations than those awayfrom the highway. In addition, a correlation was established between plant available metal concentrations and plant metaluptake concentrations.Analysis of fertilizer and manure showed considerable amountof metals (fertilizer with Pb: 1.53±0.06 mg kg^-1 andCd: 0.038 mg kg^-1 and manure with Pb: 2.55–3.34 mgkg^-1 and Cd: 0.14–0.31 mg kg^-1). Long termsimultaneous application of fertilizer and manure on thecommercial farm showed higher metal accumulation in the soiland plants than those of co-operative farm Considerableconcentrations of metals (Pb: 1.60–2.94 mg kg^-1 andCd: 0.025–0.19 mg kg^-1) were observed in fodder. The finding clearly demonstrated that there are seasonalvariation in total daily metal intake by individual cow (Pb:109.37 mg day^-1 (dry), 273.47 mg day^-1 (rainy) andCd: 2.02 mg day^-1 (dry), 19.62 mg day^-1 (rainy)).The provisional tolerable weekly intake of heavy metals incows is 390 g Pb and 28 g Cd per kg bodyweight in the rainy season and 156 g Pb and 2 gCd per kg body weight in the dry season. The levels of metals (Pb: 0.014 mg L^-1 and Cd: not detectable) and bio-transferfactor (10^-5–10^-4) in raw milk were found to be well below the Codex Alimentarius Commissions Draft (1997). Ouranalysis revealed that improvements on farm management give significant reduction in elevated levels of Pb and Cdin soil and plants, and however leads to minimize the amountof Pb and Cd in consumed milk.     

Bioindicator organisms: Heavy metal pollution evaluation in the Ionian Sea (Mediterranean Sea—Italy)

Trace metal concentrations of mercury, cadmium, lead and chromium in Patella caerulea, and Mullus barbatus were investigated to provide information on pollution of Ionian Sea, since these metals have the highest toxic potential. High chromium levels (0.47–0.97 g g^–1 ww) were registered in limpet samples collected from two station near the Gulf of Taranto, while elevated concentration of mercury (0.31–1.50 g g^–1 ww) were found in mullet specimens from Sicily. The metal concentrations recorded at the clean stations may be considered as useful background levels to which to refer for comparison within the Mediterranean area. On the contrary, the high levels of chromium and mercury found respectively in the areas near the Gulf of Taranto and at Capo Passero being of concern in terms of environmental health need frequent monitoring.     

Long term monitoring of pollutants in eggs of Yellow-legged Herring Gull from Capraia island (Tuscan Archipelago)

Chlorinated hydrocarbons (hexachlorobenzene, lindane, ppDDE, polychlorinated biphenyls) and trace elements (Hg, Se, Cd, Pb) were determined in eggs of Yellow-legged Herring Gull (Larus cachinnans) collected in an island of the Tyrrhenian Sea during the period 1981–1986. PCBs levels vary on the average between 30.4g g^–1 d.w. in 1981 to 56.1 g g^–1 d.w. in 1983. The capillary chromatograms revealed the presence of about 30 somers of PCBs without significant variations in the eggs of the same year; more than 50% of the residues is made up only three isomers: the 22'44'55', the 22'344'5' and the 22'344'55'. Average DDE residues were 7–8 times lower than those of PCBs and declined during the period (from 9.2 g g^–1 d.w. in 1981 to 4.5 g g^–1 d.w. in 1986). Cadmium and lead are present in low concentrations. The average levels of mercury and selenium are around 2–2.5 g g^–1 d.w., and a cumulative correlation, on a molar basis, exists between these two elements.     

Remote measurement of NO2 in the brown cloud over Albuquerque,New Mexico

Remote measurements of nitrogen dioxide (NO₂) were recorded in the brown cloud over Albuquerque, NM, using absorption spectroscopy in the winter of 1987-88 and summer of 1989. The NO₂ burdens (optical densities) measured in this manner were found to be in excess of 100 ppm-m. These long pathlength measurements correspond to total concentrations of approximately 5–10 ppb over the integrated observation pathlengths, which ranged from 10–20 km. These concentrations compare well with single location, independent NO _x analyses. Using two correlation (absorption) spectrometers simultaneously, it was shown that the NO₂ distribution is not uniform over the city and can change on the order of minutes in the boundary layer late in the day, demonstrating the advantages of NO₂ optical measurements for assessing the location and extent of urban nitrogen dioxide levels in the boundary layer.     

CHANGES IN ACID PRECIPITATION-RELATED WATER CHEMISTRY OF LAKES FROM SOUTHWESTERN NEW BRUNSWICK, CANADA, 1986–2001

Between 1986 and 2001, thirty-nine lakes in southwestern New Brunswick in Atlantic Canada were surveyed for acid precipitation-related water quality changes. Most of the study lakes are located on granite bedrock and represent the most acid sensitive lakes in the province. Between 1987 and 1992, hydrogen ion deposition to the lake study area averaged 452 eq ha^–1 yr^–1, compared to 338 eq ha^–1 yr^–1 between 1993 and 2000, a 25% reduction. The lake chemistry data were evaluated by dividing the lakes into four clusters for each survey year based on their acid neutralizing capacity. Twenty percent of the lakes (cluster IV) had an average ANC of 40 eq L^–1or greater and maintained an average pH of greater than 6 over the duration of the study period. A pH of 6 or greater is considered a healthy benchmark for maintaining biodiversity. The remaining 31 lakes (clusters I to III) had an average ANC of less than 40 eq L^–1and maintained an average pH of less than 6. Other lake chemistry changes included a general decline in lake sulphate and colour over the duration of the survey period, followed by more recent improvements in calcium ion, pH and ANC, and notably higher but declining aluminum levels in lower ANC and pH lakes. Nitrate accounted for 37% of the acid deposition to the study area, however it was not detectable in the lakes. Although acid deposition has declined and these lakes are beginning to show signs of acid recovery, 80% of the study lakes remain acid sensitive having little buffering capacity with low calcium, pH and ANC.     

Heavy metal concentration in the moss Pleurozium schreberi in the Niepołomice Forest,Poland: changes during 20 years

The Niepoomice Forest is a large forestcomplex (110 km²) situated in southern Poland 10 to 30 kmto the east of the urban industrial Kraków agglomeration andsteelworks, which was built up on the outskirts of the city in1950. Due to prevailing westerly winds, the forest is affectedby pollutants emitted by both the steelworks and the city. Thelevel of heavy metal contamination in the Niepoomice Forestwas described using a sensitive bioindicator – the moss Pleurozium schreberi. Mean concentrations of metals in mosscollected in the Niepoomice Forest were Cd – 0.71, Cr – 2.4,Cu – 8.6, Fe – 673, Pb – 12.7, and Zn – 61 mg/kg.Concentrations of heavy metals in moss in the NiepoomiceForest decreased in time. As compared with the relatively cleanarea in north-eastern Poland (Puszcza Biaowieska), the concentration of Fe was 2–9 fold and Pb 4–6 fold higher in theNiepoomice Forest in 1975, while in 1998 4 fold and 2 fold,respectively. In both 1975 and 1998 the most polluted by heavymetals was the western part of the Niepoomice Forest (closestto the pollution sources) and the area along the roads insidethe forest complex.     

The prevalence of bacterial resistance in clinical, food, water and some environmental samples in Southwest Nigeria

The resistance pattern and mechanisms of bacterial isolates obtained from clinical origin, soil, industrial effluent, orange juice products and drinking water were studied using commonly used antibiotics. The microbial load of the water samples, industrial effluent and orange juice products were 1.0 × 10¹–2.25 × 10⁶, 2.15 × 10⁵, and 3.5 × 10⁴–2.15 × 10⁵ cfu mL^–1, respectively. The faecal coliform test revealed that only two out of twenty orange juice products had MPN of 2 and 20, the MPN of water ranged from 1–1800, while the effluent had MPN of 1800. The bacterial isolates that were isolated include E. coli, S. aureus, P. vulgaris, S. marcescens, S. pyogenes, B. cereus, B. subtilis, Micrococcus sp., Klebsiella sp., P. aeruginosa, and Enterobacter sp. Also, clinical and soil isolates of P. aeruginosa were used in the study. Among the eight antibiotics tested for resistance on five strains of each bacterium, seven different resistance patterns were observed among the bacterial isolates obtained from water, effluent and orange juice products. Among the clinical and soil isolates of P. aeruginosa, four multiple-drug resistance patterns were obtained. Thirty strains of E. coli and S. aureus were tested for -lactamase production and fourteen strains, seven each of E. coli and S. aureus that had high Minimum Inhibitory Concentration values (MIC) for both Amoxycillin and Cloxacillin were positive.     

Factors affecting N and P losses from small catchments (Lithuania)

Most of the important factors causing differences in nutrient losses and their interaction were analysed in three small catchments that are located in partially different geographic and climatic conditions in Lithuania. The investigation revealed that climatic factors change the amount and pattern of water discharge over year (larger water discharge during winter in the catchment located closer to the sea), but nutrient leaching is more dependent on land use. Agricultural factors, such as larger cultivated area and excessive fertilisation in one catchment cause larger nitrogen losses (15 kg N ha^–1 year^–1). Large area of non-intensively used grassland leads to very small nitrogen losses (5.7 kg N ha^–1 year^–1) in another catchment. However, larger water discharge combined with loamy sandy soils leads to comparatively high nitrogen losses (12 kg N ha^–1 year^–1). The highest P losses (0.318 kg P ha^–1 year^–1) occurred in the catchment with hilly relief and clay soil texture. In summary, extensive agriculture in the post-Soviet countries has reduced the importance of agricultural activity for the extent of nutrient losses and agricultural factors (cultivation, fertilisation and livestock density) are responsible for the losses only in the region of sufficient agricultural activity (N input – 71.5 kg N ha^–1, livestock density – 0.87 LU ha^–1).     

Quality of drinking water in the Aligarh Muslim University Campus,Aligarh, U.P. (India) with respect to heavy metals

The physico-chemical characteristics of the drinking water in nine residential halls of the Aligarh Muslim University, Aligarh, U.P. (India), were studied. Nine samples each of running and standing water were taken four times over a period of one month at weekly intervals from all of the residential halls and were analysed for physico-chemical characteristics and heavy metal contents. The temperature, pH and electrical conductivity of water samples ranged between 20.0–26.0°C; 7.00–8.00 and 116.00–199.04 micromhos cm^–1 respectively whereas the values of total alkalinity, total hardness, Cl^–, SO ₄ ^– , F^–, NH₃–N, NO₂–N; NO₃–N were found between 261.00–396.00; 128.00–200.00; 8.00–69.00; 12.00–46.00; 0.90–1.35; 0.20–0.44; ND; 1.60–6.50 mg l^–1 respectively. The ranges of heavy metal concentrations in the running water samples were as follows: Cd (0.70–3.75); Cr (ND-5.00); Co (9.50–18.75); Cu (0.75–15.00); Fe (ND-13.50); Mn (3.50–51.00); Ni (7.00–17.50); Pb (0.50–2.50) and Zn (10.00–176.50) g l^–1. The heavy metal concentrations in standing water samples were found to be: Cd (1.20–4.90); Cr (ND-10.00); Co (10.25–19.00); Cu (1.75–20.00); Fe (ND-18.00); Mn (5.00–66.50); Ni (8.75–19.75); Pb (0.75–5.50) and Zn (28.60–364.00) g l^–1. The concentrations of heavy metals in drinking water supplies of the Aligarh Muslim University campus were well below the guidelines for drinking water quality as prescribed by World Health Organisation (1984). It is evident from the results that the drinking water may not cause any significant health hazard to water consumers due to heavy metals but these may be hazardous if they get accumulated in the body due to continuous consumption of water.     

DNA adducts as early bioindicators of chemical exposure

Sensitive analytical methods indicate the presence of hundreds of chemical contaminants in our environment. However, concentration of these pollutants is usually at the low parts per million or parts per billion level. At such low levels, toxicants induce long-term (chronic) rather than short-term (acute) toxicities. Experiments are designed to evaluate chronic toxicity using early bioindicators. Recently, fish have been used as experimental animals because some species show early (weeks as opposed to years in other research animals), sensitive responses. Thus, medaka (Oryzias latipes), following exposure to diethylnitrosamine (DEN), exhibited liver tumors in several weeks; more interestingly its DNA was modified (to a DNA-adduct) after only 24–48 hours exposure. Such adducts show promise as early bioindicators because they are formed within hours of exposure. The formation of DNA-adducts were monitored in medaka and rainbow trout (Salmo gairdneri) exposed to DEN by aqueous or intra-peritoneal routes. Using HPLC-Fluorimetry, O ⁶-ethylguanine (O ⁶-EtGua) was detected and monitored in acid thermal hydrolysates of DNA isolates. (Detection limit for O ⁶-EtGua was as low as 3 ng, 1.7×10^-11 moles). Fourier transform cyclotron resonance mass spectrometry with IR laser desorption/ionization was used advantageously to establish the structure of nucleotides, bases and nucleosides directly, without further cumbersome derivatizations. Other aspects of DNA-adducts are discussed.