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.     

The effects of salinity,temperature and sediment on the toxicity of copper to juvenile Hediste (Nereis) diversicolor (O. F. Muller)

Without sediment, increasing salinity (7.3 to 29.2) and increasing temperature (12 to 22 °C) reduced the toxicity of copper to juvenile Hediste diversicolor. The LC₅₀ values ranged from 357 gL^-1 in 7.3 to 513 g L^-1 in 29.2 at 12°C and from 247 to 500 g L^-1 at 22°C. In deionized water all the juvenile were dead in all solutions to which copper was added (100 to 600 g L^-1). Dead worms were swollen and everted their pharynxs. In higher doses of copper (500 to 600 g L^-1) the worms were abnormal in behaviour in all salinities (0 to 29.2). The ability to swim or crawl was disturbed.With sediments increasing temperature and increasing salinity increased the toxicity of copper to the worms. The LC₅₀ values ranged from 3200 to 4100 g L^-1 at 22°C. The response of the juvenile to copper was antagonistic to increasing temperature and salinity and synergistic to increasing salinity and increasing temperature without and with the sediment respectively.     

Characterization of atmospheric dust at Gurushikar,Mt. Abu,Rajasthan

The nature of atmospheric aerosols at Gurushikar, Mt. Abu, Rajasthan where a gamma ray telescope is to be installed, was investigated. Air particulate samples collected on filters were used to estimate the total suspended particulate matter (TSPM) and its elemental composition. The TSPM varied from 31 to 103 g/m³ during January to March 1994. The heighest loads were observed during the months of May and June (80–100 g/m³) and lowest during October (20–60 g/m³). The dust was also examined for size, shape and nature of the mineral matter. The particle sizes varied from 100 m to 5 m. The course particles (>50 m) are irregular shaped quartz grains. Some of the medium size (=50 m) particles were spherical and were highly conducting. These particles were rich in iron content. Correlation coefficients among various elements in the dust showed that it is made up of mainly two components-wind blown ground dust and particulate arising out of wood and coal burning.     

Respiratory Suspended Particulate (RSP) Concentration and its Implications to Roadside Workers: A Case Study of Hong Kong

The adsorption behaviour of Diphenylamine (DPAM), napthylamine ( NAM), napthylamine ( NAM)and aniline on pyrolusite and activated carbon has been studied.Pyrolusite shows remarkable sorption capacity for DPAM and NAM as compared to aniline; (the adsorption followed theorder:Activated Carbon: DPAM = NAM > AnilinePyrolusite: DPAM: NAM > NAM> Aniline)The maximum adsorption of NAM occurred in theconcentration range 4–20 g mL^-1 on pyrolusite (95%)and 4–50 g mL^-1 on activated carbon (100%). Theeffect of various doses of activated carbon on the adsorption of NAM confirm Langmuir and Freundlich isotherms where asFreundlich isotherm is obeyed by pyrolusite. The adsorption of NAM on both the absorbents is not affected in presence ofDPAM over a wide range of their initial concentrations (20–60g mL^-1). The desorption studies of NAM onpyrolusite was carried out by batch as well as column processes.Excellent results were obtained when a mixture of n-hexane andisopropanol (91:1) was used as eluent.     

Insecticide Contamination of Jamaican Environment. V. Island-Wide Rapid Survey of Residues in Surface and Ground Water

Residues of organochlorines and organophosphates were determined by gas chromatography in water and sediment from 26 locations in 17 major rivers, 7 natural springs and 13 wells across Jamaica. Samples were collected on only one occasion between May and July, 1994. Residues of endosulfan were detected in all but three rivers; -endosulfan in 15 samples of sediment (0.9–108.1, mean = 28.93, S.E. = 7.198 g kg-1) and 13 of water (0.01–0.35, mean = 0.11, S.E. = 0.035 g L-1), -endosulfan in 5 sediment (15.29–49.35, mean = 30.56, S.E. = 7.132 g kg-1) and 12 water (0.05–0.31, mean = 0.14, S.E. = 0.031 g L-1) samples, and endosulfan sulphate in waters of three rivers (0.003–0.244 g L-1). Chlorpyrifos was present in 9 sediment (0.423-135.2, mean = 18.38, S.E. = 10.699 g kg-1) and two water (0.001–0.022 g L-1) samples, diazinon and ethoprophos in the sediment of one river each. Mean levels (g L-1) of and isomers and sulphate of endosulfan were 0.16 (S.E. = 0.057), 0.12 (S.E. = 0.036) and 0.15 (S.E. = 0.089), respectively, in four of the seven springs and 0.23 (S.E. = 0.052), 0.11 (S.E. = 0.029) and 0.26 (S.E. = 0.088), respectively, in seven of the thirteen wells monitored.     

Environmental Contaminants in Blood, Hair, and Tissues of Ocelots from the Lower Rio Grande Valley, Texas, 1986–1997

The ocelot (Felis pardalis) isan endangered neotropical cat distributed within asmall range in the Lower Rio Grande Valley (LRGV), inTexas, U.S.A. Studies of the impacts of environmentalcontaminants in wild cats are few. Approximately onefourth of the estimated population (about 100) ofocelots in the LRGV was sampled to evaluate theimpacts of chlorinated pesticides, polychlorinatedbiphenyls, and trace elements on the population. Hairwas collected from 32 ocelots trapped between 1986–1992,and blood was collected from 20 ocelots trappedbetween 1993–1997. A few blood samples were obtainedfrom individuals recaptured two or three times. Tissue samples from 4 road-killed ocelots were alsoanalyzed. DDE, PCBs, and Hg were some of the mostcommon contaminants detected in hair and blood. MeanHg levels in hair ranged from 0.5 to 1.25 g g^-1 dw,Se from 1.5 to 3.48 g g^-1 dw, and Pb from 0.56 to26.8 g g^-1 dw. Mean DDE concentrations in plasma ranged from 0.005 g g^-1 ww to 0.153 g g^-1 ww, and PCBs ranged from 0.006 g g^-1 ww to 0.092 g g^-1 ww. Mean Hg levels in red blood cells rangedfrom 0.056 g g^-1 dw to 0.25 g g^-1 dw. Concentrations of DDE, PCBs, or Hg, did not increasesignificantly with age, although the highestconcentrations of DDE and Hg were found in olderanimals. Overall, concentrations of DDE, PCBs, and Hgwere low and at levels that currently do not pose anythreat to health or survival of the ocelot. This isfurther supported by good reproduction of the ocelotin the LRGV, where adult females averaged about 1.5kittens/litter. Thus, it seems that the current majorthreat to recovery of the ocelot in the LRGV may behabitat loss, although potential impacts of newgeneration pesticides, such as organophosphorus andcarbamate insecticides need further study.     

Aldehyde Concentrations in Ambient Air of Coastal Georgia, U.S.A.

Aldehydes are an airborne byproduct of many industrialprocesses, vehicle transportation, and emissions fromnumerous natural sources. To characterize aldehydeconcentrations in ambient air of the Savannah, Georgiaarea, air samples for 3 aldehydes (formaldehyde,acetaldehyde, and propionaldehyde) were collected atfive sites on a monthly basis over a 12-month periodfrom December of 1995 through November 1996. Four ofthe sites were in central Savannah and the fifth sitewas located in a rural area about 56 km south ofSavannah. During each 24-hr sampling episode, sampleswere collected in two 12-hr periods approximatingdaylight and nighttime hours, following U.S. EPAMethod TO-11. Formaldehyde concentrations ranged from0.17 to 6.80 g m^-3, acetaldehydeconcentrations ranged from 0.07 to7.60 g m^-3, and propionaldehyde levels rangedfrom 0.02 to 9.10 g m^-3. On average, thefour sites in Savannah had higher aldehydeconcentrations than the rural site (2.0 versus1.2 g m^-3 for formaldehyde, 2.3 versus1.7 g m^-3 for acetaldehyde, and 1.2 versus1.0 g m^-3 for propionaldehyde). The daytimeconcentrations for formaldehyde and acetaldehyde werehigher than the nighttime levels. The data from allthe sites were within published worldwide backgroundvalues for aldehydes.     

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.     

The monitoring of cadmium,zinc and copper in the kidneys and liver of humans deceased in the region of Cracow (Poland)

Cadmium, zinc and copper levels were determined in the renal cortex and liver of 60 inhabitants of Cracow, Poland. Cadmium levels in the renal cortex were contained in broad limits of 5–176 g/g, mean 50.6 g/g (wet weight). Maximum levels were found in the age group of about 50–60 years. The levels were slightly higher in men (53 g/g) than in women (45 g/g), with no effect of location within the region. The levels in smokers (62 g/g) were much higher than in non-smokers (32 g/g). The above relations were less pronounced for cadmium levels in the liver. Whole body retention of cadmium followed the pattern of cadmium in renal cortex. The level of zinc in renal cortex reflected those of cadmium. A significant proportion of the population (54% in smokers, 9% in non-smokers) showed cadmium levels in renal cortex exceeding the reference level of 50 g/g recently accepted for general population. In the view of the authors the exposure to cadmium of the population of Cracow is excessive and calls for attention.The study was performed under a KBN grant No 40106 91 01.     

Trihalomethane Formation Potential and Concentration Changes During Water Treatment at Mumbai (India)

The treated water at the outlet oftreatment plants and representative servicereservoirs of Mumbai city have been evaluatedfor trihalomethane formation potential in1995–1996. Chloroform, dichlorobromomethane,chlorodibromomethane and bromoform have beenmonitored during monsoon, winter and summer.The levels of chloroform are found above theregulated WHO guideline value of 200 g L^-1 in final water during postmonsoon atGhatkopar (226 g L^-1), Malbar (210.3 g L^-1) and Tulsi (231.26 g L^-1).     

Roadside Concentration of Gaseous and Particulate Matter Pollutants and Risk Assessment in Dar-Es-Salaam, Tanzania

This study used manual air sampling method to assess the contribution of road traffic to air pollution level in Dar-es-Salaam City, Tanzania. Samples were collected from 11 different sites. Parameters measured were: sulphur dioxide using pararosaniline method, nitrogen dioxide using saltzman method, particulate matter and particulate lead using filtration method and atomic absorption spectrometric method, respectively. Results showed that hourly average sulphur dioxide concentration range from 127 to 1385 g/m³. The measured values of sulphur dioxide were above the recommended WHO guidelines with an hourly objective value of 350 g/m³ at 87% of the sampling sites. The hourly average nitrogen dioxide concentration ranged from 18 to 53 g/m³. The maximum hourly nitrogen dioxide concentration at 53 g/m³ was below the WHO guideline value of 200 g/m³. The hourly average suspended particulate matter (SPM) ranged from 98 to 1161 g/m³, exceeding the recommended value of 230 g/m³ by WHO at 87% of the sampling sites. The hourly average lead concentration was found to range from 0.60 to 25.6 g/m³, exceeding again the WHO guideline value of 1.5 g/m³at 83% of the sampling sites. Results predicted by Gaussian model when compared with the measured values were found to have a correlation coefficient of 0.8, signifying a good correlation. The risk assessment was undertaken considering the people who spend a significant portion of their time near the roads, such as the Uhuru primary school pupils and the adult population who reside by the roadside. The unit risk realised was 18.2 × 10^–6 for adult population and 2.2 × 10^–6 for pupils, both scenarios showing risk higher than the United Sates of America Environmental Protection Agency (USEPA) acceptable limit of 1× 10^–6. Considering the magnitude of the problem at hand, this study recommends an introduction of mandatory emission tests of SPM, lead and sulphur dioxide (SO₂). The study further recommends the introduction of continuous and/or regular air quality monitoring and the use non-leaded petrol in Tanzania.     

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.     

Measurements of Ozone Concentrations in Zagreb

Ozone concentrations were measured in Zagreb at four sites from May 1999 to April 2001 in order to categorize the air quality with respect to ozone. In the summer of 2000, the ozone measurements were also extended to four sites in the suburbs of Zagreb. Methods of active and passive sampling with nitrite ion as a reagent were used. In the northern part of the town ozone was analyzed by an automatic device. Automatic device measurements in the years 1999 and 2000 showed that hourly averages of ozone concentrations did not exceed the Croatian recommended value of the 98th percentile (180 g m^–3). Over the two-year period, 24-h averages occasionally exceed 110 g m^–3 in city center and in the northern part of the town. Regardless of these isolated examples, ozone was well within acceptable concentrations. Ozone concentrations measured in summer 2000 were higher in the suburbs of Zagreb than in the city. The 98th percentile values higher than 110 g m^–3 were recorded at three sites.     

Methane in ocean waters: Concentration and carbon isotope variability at East Pacific Rise and in the Arabian Sea

Methane concentrations and stable carbon isotope ratios of water samples from the East Pacific Rise (EPR) at 21°S and the Arabian Sea (24°N, 65°E) have been determined. EPR surface water is in equilibrium (ca. 50 nl/L and –50<¹³CH₄<–46) with atmospheric methane. Deep background water has the signature of the remaining fraction of atmospheric methane partially oxidized in the water column by bacteria. Bottom near, hydrothermally influenced vent methane (>100nl/L and –30<¹³CH₄<–22) is detectable only close to the seep site. There is no input of hydrothermal methane into the atmosphere. EPR water is considered to be rather a sink than a source of atmospheric methane. Surface waters of the Arabian Sea are enriched in methane relative to the atmosphere (source for atmospheric methane). Carbon isotope ratios point to a bacterial origin of methane (¹³CH₄<–55) that is generated in the surface waters. Concentration changes and variations of carbon isotope ratios also suggest that methane seeping from the sea floor sediments of the Arabian Sea is oxidized by bacterial activity and does not reach the atmosphere.     

Effect of Common Pesticides Used in the Niger Delta Basin of Southern Nigeria on Soil Microbial Populations

The effects of eleven pesticides on the populations of bacteria, actinomycetes, fungi and protozoa was investigated by treating a garden soil with their recommended rates. The microbial populations were estimated using the standard plate-count technique. Of the ll pesticides investigated, phenylmercuric acetate (agrosan) at 50 g g^-1 inhibited bacterial density the most, i.e. from 4,600,000 to 220 cells g^-1. The pesticides were Pentachloronitrobenzene (PCNB), tetramethylmethylthiuram disulphide (thiram),1- naphthylmethylcarbamate (Vetox 85), 1,2,3,4,5,6-hexachlorocyclohexane (Gammalin 20), phenylmercuric acetate (Agrosan), tetrachloroterephthalic acid (Dacthal), 4-nitrophenyl –2-nitro-4-trifluoromethylphenyl ether (Preforan), 2-ethyl-6-methyl –N-2-methoxy –1-methyl ethyl-chloroacetanide (Dual), Benlate, Brestan and Gramoxone. Pentachloronitrobenzene (PCNB) at 240,000 g g^-1 reduced bacterial population from 4,600,000 to 2,100 cells g^-1, whereas tetramethylthiuram disulphide (thiram) at 100 g g^-1 suppressed it by 2 log orders of magnitude. Soil application of 1-naphthylmethylcarbamate (Vetox 85) at 100 g g^-1 and 1,2,3,4,5,6,-hexachlorocyclohexane (Gamalin 20) at 1,300 g g^-1 repressed the bacterial numbers by 2 log orders of magnitude each. Pentachloronitrobenzene reduced the actinomycetes density from 340,000 to 320 cells g^-1 and completely eliminated all fungal and protozoan propagules from the soil. The Gammalin 20 completely wiped out all the fungi, whereas phenylmercuric acetate totally eliminated all the protozoa and reduced the fungal population from 34,000 to 60 cells g^-1. In general, protozoa and fungi were more susceptible to fungicides than bacteria and actinomycetes. Pentachloronitrobenzene, 1,2,3,4,5,6,-hexachlorocyclohexane and phenylmercuric acetate were toxic particularly to soil microorganisms, whereas the herbicides dacthal, Preforan and Dual were quite harmless in soil at application rates of 0.1, 0.06 and 0.02 g g^-1 respectively.     

Using Mussel Isotope Ratios to Assess Anthropogenic Nitrogen Inputs to Freshwater Ecosystems

Stable nitrogen isotope ratios (¹⁵N) of freshwater mussels from a series of lakes and ponds wererelated to watershed land use characteristics to assess their utility in determining the source ofnitrogen inputs to inland water bodies. Nitrogen isotope ratiosmeasured in freshwater musselsfrom 19 lakes and ponds in Rhode Island, U.S.A., ranged from4.9–12.6 and were found tosignificantly correlate with the fraction of residential development in 100 and 200 m bufferzones around the ponds. Mussel ¹⁵N values in 12 of the 19 ponds also showed significantcorrelation with average dissolved nitrate concentrations, which ranged from 23–327 g L^-1.These observations, in light of previous studies which link elevated¹⁵N values of nitrogenderived from septic wastewater with those seen in biota, suggest that mussel isotope ratios mayreflect nitrogen source in freshwater ecosystems. We followed aniterative approach usingmultiple regression analysis to assess the relationship between mussel¹⁵N and the land usecategories fraction residential development, fraction feedlotagriculture, fraction row-cropagriculture, and fraction natural vegetation in 100 and 200 m bufferzones and pond watersheds.From this we developed a simple regression model to predict mussel¹⁵N from the fraction ofresidential development in the 200 m buffer zone around the pond.Subsequent testing with datafrom 16 additional sites in the same ecoregion led us to refine themodel by incorporating thefraction of natural vegetation. The overall average absolute differencebetween measured andpredicted ¹⁵N values using the two-parameter model was 1.6. Potential sources of error inthe model include differences in the scale and categorization ofland-use data used to generate andtest the model, differences in physical characteristics, such asretention time and range ofresidential development, and exclusion of sources of enrichednitrogen such as runoff from feedlot operations or increased nitrogen loading from inefficient or failed septic systems.     

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.     

Monitoring for 2,4-residues in fish species resident in treated lakes in east-central Ontario 1977–80

Authorized use of 2,4-D by cottage owners in Buckhorn Lake for the years 1977 to 1980 ranged from 124 to 280 kg of active ingredient, annually. This would give predicted average water concentrations of 2 to 4 g L^–1 during the June–July period. However, higher residues were observed in the Lake. Between 1977 and 1980, 353 individual fish, of eight species, were caught for analysis in Buckhorn and Chemong lakes. These fish belonged to eight edible species. Twelve percent of the fish caught during the pre-treatment period (i.e. May), had detectable residues of 2,4-D. Mean residues by species and year ranged from <5 to 30 g kg^–1 2,4-D. In the early post-treatment period (i.e. July), 69% of fish caught had mean residues by species which ranged from <5 to 136 g kg^–1 2,4-D. In the late post-treatment period (i.e. October), 19% of fish caught by year had detectable residues of 2,4-D. Mean residues by species during this period ranged from <5 to 60 g kg^–1 2,4-D. While 15 (i.e. 4%) of the 353 fish and fish composites had 2,4-D above the maximum residue limit of 100 g kg^–1 only six were of edible size.     

Intake of Chromium by the Adult Population of Mumbai City

Electro Thermal Atomic Absorption Spectrophotometry (ET-AAS), is used for the determination of chromium (Cr) in a variety of environmental matrices. The detection limit for the estimation of Cr is 2 pg absolute for a volume injection of 20 l. The precision of the method is established by analysing Cr from a synthetic mixture containing various elements in different qualities (0.5–10 ppm) and is found to be within ± 8%. The reliability of estimation is further assessed through the analysis of Standard Reference Materials (SRMs) of soil, hay, milk powder and lake sediment obtained from IAEA.The total intake of Cr through air, water and food works out to be 54 g/day for the adult population of Mumbai city. The dietary intake through food is the major contributor to the total intake of Cr. The concentration of Cr in atmospheric air and drinking water collected from different suburbs showed geometric mean concentrations of 0.09 g/m³ and 0.3 g/l, respectively. The daily intake of Cr, though lower, is closer to the lower bound of the recommended value of 50–200 g/day.     

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.