Seasonal and interannual variations of nitrate and chloride in stream waters related to spatial and temporal patterns of groundwater concentrations in agricultural catchments

Nitrate concentrations in streamwater of agricultural catchments often exhibit interannual variations, which are supposed to result from land‐use changes, as well as seasonal variations mainly explained by the effect of hydrological and biogeochemical cycles. In catchments on impervious bedrock, seasonal variations of nitrate concentrations in streamwater are usually characterized by higher nitrate concentrations in winter than in summer. However, intermediate or inverse cycles with higher concentrations in summer are sometimes observed. An experimental study was carried out to assess the mechanisms that determine the seasonal cycles of streamwater nitrate concentrations in intensive agricultural catchments. Temporal and spatial patterns of groundwater concentrations were investigated in two adjacent catchments located in south‐western Brittany (France), characterized by different seasonal variations of streamwater nitrate concentrations. Wells were drilled across the hillslope at depths ranging from 1·5 to 20 m. Dynamics of the water table were monitored and the groundwater nitrate and chloride concentrations were measured weekly over 2 years. Results highlighted that groundwater was partitioned into downslope domains, where denitrification induced lower nitrate concentrations than into mid‐slope and upslope domains. For one catchment, high subsurface flow with high nitrate concentrations during high water periods and active denitrification during low water periods explained the higher streamwater nitrate concentrations in winter than in summer. For the other catchment, the high contribution of groundwater with high nitrate concentrations smoothed or inverted this trend. Increasing bromide/chloride ratio and nitrate concentrations with depth argued for an effect of past agricultural pressure on this catchment. The relative contribution of flows in time and correlatively the spatial origin of waters, function of the depth and the location on the hillslope, and their chemical characteristics control seasonal cycles of streamwater nitrate concentrations and can influence their interannual trends. Copyright © 2004 John Wiley & Sons, Ltd.     

Assessing background ground water chemistry beneath a new unsewered subdivision

Previous site-specific studies designed to assess the impacts of unsewered subdivisions on ground water quality have relied on upgradient monitoring wells or very limited background data to characterize conditions prior to development. In this study, an extensive monitoring program was designed to document ground water conditions prior to construction of a rural subdivision in south-central Wisconsin. Previous agricultural land use has impacted ground water quality; concentrations of chloride, nitrate-nitrogen, and atrazine ranged from below the level of detection to 296 mg/L, 36 mg/L, and 0.8 microg/L, respectively, and were highly variable from well to well and through time. Seasonal variations in recharge, surface topography, aquifer heterogeneities, surficial loading patterns, and well casing depth explain observed variations in ground water chemistry. This variability would not have been detected if background conditions were determined from only a few monitoring wells or inferred from wells located upgradient of the subdivision site. This project demonstrates the importance of characterizing both ground water quality and chemical variability prior to land-use change to detect any changes once homes are constructed.     

Predicting ground water nitrate concentration from land use

Ground water nitrate concentrations on Nantucket Island, Massachusetts, were analyzed to assess the effects of land use on ground water quality. Exploratory data analysis was applied to historic ground water nitrate concentrations to determine spatial and temporal trends. Maximum likelihood Tobit and logistic regression analyses of explanatory variables that characterize land use within a 1000-foot radius of each well were used to develop predictive equations for nitrate concentration at 69 wells. The results demonstrate that historic nitrate concentrations downgradient from agricultural land are significantly higher than nitrate concentrations elsewhere. Tobit regression results demonstrate that the number of septic tanks and the percentages of forest, undeveloped, and high-density residential land within a 1000-foot radius of a well are reliable predictors of nitrate concentration in ground water. Similarly, logistic regression revealed that the percentages of forest, undeveloped, and low-density residential land are good indicators of ground water nitrate concentration > 2 mg/L. The methodology and results outlined here provide a useful tool for land managers in communities with shallow water tables overlain with highly permeable materials to evaluate potential effects of development on ground water quality.     

Variations of bromide in potable ground water in the United States

Concentrations of bromide in potable ground water that has <10 mg/L chloride range from 0.0032 to 0.058 mg/L with a median value of 0.016 mg/L. The chloride/bromide mass ratio for the same water ranges from 43 to 285 with a median value of 101. The ratios, which resulted from screening approximately 165 analyses of water from 32 locations in 24 states in the United States, show a distinct geographic variation with highest values near the coast and trending toward a value of approximately 50 in the continental interior.     

Hydrogen Peroxide Treatment of Septic Systems and Its Negative Effects on Shallow Ground Water

Soil-solution samplers and shallow ground water monitoring wells were utilized to monitor nitrate movement to ground water following H₂O₂ application to a clogged soil absorption system. Nitrate-nitrogen concentrations in soil water and shallow ground water ranged from 29 to 67 mg/L and 9 to 22 mg/L, respectively, prior to H₂O₂ treatment. Mean nitrate-nitrogen concentrations in soil water and ground water increased and ranged from 67 to 115 mg/L and 23 to 37 mg/L, respectively, one week after H₂O₂ application. Elevated concentrations of nitrate-nitrogen above background persisted for several weeks following H₂O₂ treatment. The H₂O₂ treatment was unsuccessful in restoring the infiltrative capacity of a well-structured soil. Application of H₂O₂ to the soil absorption system poses a threat of nitrate contamination of ground water and its usefulness should be fully evaluated before rehabilitation is attempted.     

Characterising deep vadose zone water movement and solute transport under typical irrigated cropland in the North China Plain

Understanding the dynamics and mechanisms of soil water movement and solute transport is essential for accurately estimating recharge rates and evaluating the impacts of agricultural activities on groundwater resources. In a thick vadose zone (0–15 m) under irrigated cropland in the piedmont region of the North China Plain, soil water content, matric potential, and solute concentrations were measured. Based on these data, the dynamics of soil water and solutes were analysed to investigate the mechanisms of soil water and solute transport. The study showed that the 0–15‐m vadose zone can be divided into three layers: an infiltration and evaporation layer (0–2 m), an unsteady infiltration layer (2–6 m), and a quasi‐steady infiltration layer (6–15 m). The chloride, nitrate, and sulphate concentrations all showed greater variations in the upper soil layer (0–1 m) compared to values in the deep vadose zone (below 2 m). The average concentrations of these three anions in the deep vadose zone varied insignificantly with depth and approached values of 125, 242, and 116 mg/L. The accumulated chloride, sulphate, and nitrate were 2,179 ± 113, 1,760 ± 383, and 4,074 ± 421 kg/ha, respectively. The soil water potential and solute concentrations indicated that uniform flow and preferential flow both occurred in the deep vadose zone, and uniform flow was the dominant mechanism of soil water movement in this study. The piston‐like flow velocity of solute transport was 1.14 m per year, and the average value of calculated leached nitrate nitrogen was 107 kg/ha?year below the root zone. The results can be used to better understand recharge processes and improve groundwater resources management.     

High-permeability layers for remediation of ground water; go wide, not deep

A nitrate-reactive porous media layer comprising wood particles with very high hydraulic conductivity (K approximately 1 cm/s) was used to successfully treat nitrate in a shallow sand-and-gravel aquifer in southern Ontario. Nitrate concentrations of 1.3 to 14 mg/L as N in the aquifer were attenuated to <0.5 mg/L as N in the reactive layer. Borehole dilution testing indicated that ground water velocities in the reactive layer, although variable, averaged five times higher than in the surrounding aquifer, suggesting that the layer was capturing ground water flow from deeper in the aquifer. The use of high-K reactive media opens up the possibility of installing permeable reactive barriers as horizontal layers in the shallow water table zone that do not necessarily have to penetrate the full depth of a contaminant plume to be effective. Model simulations show that the depth of capture of a high-K layer increases as the layer width in the direction of flow increases. Shallower emplacement could decrease barrier costs at some sites.     

Assessing herbicide concentrations in the saturated and unsaturated zone of a Chalk aquifer in southern England

The behavior of the herbicides isoproturon (IPU) and chlortoluron (CTU) in ground water and shallow unsaturated zone sediments were evaluated at a site situated on the Chalk in southern England. Concentrations of IPU in ground water samples varied from < 0.05 to 0.23 microgram/L over a five-year period of monitoring, and were found to correlate with application of the pesticide. Concentrations of pesticides in ground water samples collected during periods of rising water table were significantly higher than pumped samples and suggest that rapidly infiltrating recharge water contains higher herbicide concentrations than the native ground water. Significant variations in herbicide concentrations were observed over a three-month period in ground water samples collected by an automated system, with concentrations of IPU ranging from 0.1 to 0.5 microgram/L, and concentrations of a recent application of CTU ranging from 0.2 to 0.8 microgram/L. Different extraction methods were used to assess pore water concentrations of herbicides in the unsaturated zone, and samples were analyzed by standard HPLC analysis and immunoassay (ELISA) methods. These data indicated highly variable concentrations of herbicide ranging from 4 to 200 g/ha for HPLC and 0.01 to 0.04 g/ha for ELISA, but indicate a general pattern of decreasing concentrations with depth. The results of this study indicate that transport of IPU and CTU through the unsaturated zone to shallow ground water occurs and that this transport increases immediately following herbicide application. Measured concentrations of herbicides are generally lower than specified by the European Union Drinking Water Directive, but are observed to spike above this limit. These results imply that, while delivery of pesticides to ground water can occur as a result of normal agricultural practices, the impact on potable supplies is likely to be negligible due to the potential for degradation during the relatively long travel time through the unsaturated zone and high degree of dilution that occurs within the aquifer. As a result of the wide variation in concentrations detected by different techniques, it is suggested that for future site investigations more than one sampling strategy be employed to characterize the occurrence of pesticide residues and elucidate the transport mechanisms.     

Sources of Ground Water Salinization in Parts of West Texas

Abstract
Determination of chemical constituent ratios allows distinction between two salinization mechanisms responsible for shallow saline ground water and vegetative-kill areas in parts of west Texas. Mixing of deep-basin (high Cl) salt water and shallow (low Cl) ground water results in saline waters with relatively low Ca/Cl, Mg/Cl, SO₄4/ Cl, Br/Cl, and NO₃/Cl ratios. In scattergrams of major chemical constituents vs. chloride, plots of these waters indicate trends with deep-basin brines as high Cl end members. Evaporation of ground water from a shallow water table, in contrast, results in saline water that has relatively high Ca/Cl, Mg/Cl, SO₄/Cl, and Br/CL ratios. Trends indicated by plots of this water type do not coincide with trends indicated by plots of sampled brines. Leaching of soil nitrate in areas with a shallow water table accounts for high NO₃ concentrations in shallow ground water.     

Estimating background and threshold nitrate concentrations using probability graphs

Because of the ubiquitous nature of anthropogenic nitrate (NO3(-)) in many parts of the world, determining background concentrations of NO3(-) in shallow ground water from natural sources is probably impossible in most environments. Present-day background must now include diffuse sources of NO3(-) such as disruption of soils and oxidation of organic matter, and atmospheric inputs from products of combustion and evaporation of ammonia from fertilizer and livestock waste. Anomalies can be defined as NO3(-) derived from nitrogen (N) inputs to the environment from anthropogenic activities, including synthetic fertilizers, livestock waste, and septic effluent. Cumulative probability graphs were used to identify threshold concentrations separating background and anomalous NO(3)-N concentrations and to assist in the determination of sources of N contamination for 232 spring water samples and 200 well water samples from karst aquifers. Thresholds were 0.4, 2.5, and 6.7 mg/L for spring water samples, and 0.1, 2.1, and 17 mg/L for well water samples. The 0.4 and 0.1 mg/L values are assumed to represent thresholds for present-day precipitation. Thresholds at 2.5 and 2.1 mg/L are interpreted to represent present-day background concentrations of NO(3)-N. The population of spring water samples with concentrations between 2.5 and 6.7 mg/L represents an amalgam of all sources of NO3(-) in the ground water basins that feed each spring; concentrations > 6.7 mg/L were typically samples collected soon after springtime application of synthetic fertilizer. The 17 mg/L threshold (adjusted to 15 mg/L) for well water samples is interpreted as the level above which livestock wastes dominate the N sources.     

Effects of Agriculture on Ground-Water Quality in Five Regions of the United States

Water-quality conditions in surficial unconsolidated aquifers were assessed in five agricultural regions in the United States. The assessment covers the Delmarva Peninsula, and parts of Long Island, Connecticut, Kansas, and Nebraska, and is based on water-quality and ancillary data collected during the 1980s. Concentrations of nitrate in ground water in these areas have increased because of applications of commercial fertilizers and manure. Nitrate concentrations exceed the maximum contaminant level (MCL) for drinking water of 10 milligrams per liter as nitrogen established by the U.S. Environmental Protection Agency in 12 to 46 percent of the wells sampled in the agricultural regions. Concentrations of nitrate are elevated within the upper 100 to 200 feet of the surficial aquifers. Permeable and sandy deposits that generally underlie the agricultural areas provide favorable conditions for vertical leaching of nitrate to relatively deep parts of the aquifers. The persistence of nitrate at such depths is attributed to aerobic conditions along ground-water-flow paths. Concentrations of nitrate are greatest in areas that are heavily irrigated or areas that are underlain by well-drained sediments; more fertilizer is typically applied on land with well-drained sediments than on poorly drained sediments because well-drained sediments have a low organic-matter content and low moisture capacity. Concentrations of other inorganic constituents related to agriculture, such as potassium and chloride from potash fertilizers, and calcium and magnesium from liming, also are significantly elevated in ground water beneath the agricultural areas. These constituents together impart a distinctive agricultural-chemical trademark to the ground water, different from natural water.     

Die Nitratsituation in der Bundesrepublik Deutschland

Altogether 10… 20 kg/ha·a N from precipitation are introduced into the soil. The fertilization of the agriculturally used area increased from 50 to 120 kg/ha·a N between 1950 and 1982. The nitrogen concentration is theoretically increased by 0.4 mg/l due to infiltration of surface water and wastewaters. The data prove agriculture to the main source of the nitrate load of groundwater, especially in regions with predominantly intensive agricultural use there is delivered drinking water with nitrate concentrations of more than 50 mg/l. The fixing of the limit value for drinking water at 50 mg/l nitrate (value recommended by the EC: 25 mg/l) is justified by new findings. Since the technology of nitrate elimination from water is very expensive, mainly the preventing of too high nitrate concentrations should be aimed at by agricultural measures of ground-water protection.     

Chloride source delineation in an urban-agricultural watershed: Deicing agents versus agricultural contributions

Analyses (n = 525) of chloride (Cl⁻), bromide (Br⁻), nitrate as nitrogen (NO₃-N), sodium (Na⁺), calcium (Ca²⁺) and potassium (K⁺) in stream water, tile-drain water and groundwater were conducted in an urban-agricultural watershed (10% urban/impervious, 87% agriculture) to explore potential differences in the signature of Cl⁻ originating from an urban source as compared with an agricultural source. Only during winter recharge events did measured Cl⁻ concentrations exceed the 230 mg/L chronic threshold. At base flow, nearly all surface water and tile water samples had Cl⁻ concentrations above the calculated background threshold of 18 mg/L. Mann–Whitney U tests revealed ratios of Cl⁻ to Br⁻ (p = .045), to NO₃-N (p < .0001), to Ca²⁺ (p < .0001), and to Na⁺ (p < .0001) to be significantly different between urban and agricultural waters. While Cl⁻ ratios indicate that road salt was the dominant source of Cl⁻ in the watershed, potassium chloride fertilizer contributed as an important secondary source. Deicing in watersheds where urban land use is minimal had a profound impact on Cl⁻ dynamics; however, agricultural practices contributed Cl⁻ year-round, elevating stream base flow Cl⁻ concentrations above the background level.     

Geologic controls on the chemical behaviour of nitrate in riverside alluvial aquifers,Korea

To investigate the origin and behaviour of nitrate in alluvial aquifers adjacent to Nakdong River, Korea, we chose two representative sites (Wolha and Yongdang) having similar land‐use characteristics but different geology. A total of 96 shallow groundwater samples were collected from irrigation and domestic wells tapping alluvial aquifers. About 63% of the samples analysed had nitrate concentrations that exceeded the Korean drinking water limit (44·3 mg l^?1 NO₃^?), and about 35% of the samples had nitrate concentrations that exceeded the Korean groundwater quality standard for agricultural use (88·6 mg l^?1 NO₃^?). Based on nitrogen isotope analysis, two major nitrate sources were identified: synthetic fertilizer (about 4‰ δ¹⁵N) applied to farmland, and animal manure and sewage (15–20‰ δ¹⁵N) originating from upstream residential areas. Shallow groundwater in the farmland generally had higher nitrate concentrations than those in residential areas, due to the influence of synthetic fertilizer. Nitrate concentrations at both study sites were highest near the water table and then progressively decreased with depth. Nitrate concentrations are also closely related to the geologic characteristics of the aquifer. In Yongdang, denitrification is important in regulating nitrate chemistry because of the availability of organic carbon from a silt layer (about 20 m thick) below a thin, sandy surface aquifer. In Wolha, however, conservative mixing between farmland‐recharged water and water coming from a village is suggested as the dominant process. Mixing ratios estimated based on the nitrate concentrations and the δ¹⁵N values indicate that water originating from the village affects the nitrate chemistry of the shallow groundwater underneath the farmland to a large extent. Copyright © 2003 John Wiley & Sons, Ltd.     

On the Toxicity and Biodegradation of Cationic Surfactants Über die Toxizität und den biologischen Abbau kationischer Tenside

Three ammonium halide type surfactants were tested under standard laboratory condition for biodegradability and acute toxicity to Daphnia magna and in the Microtox test with the luminescent bacterium Photobacterium phosphoreum. The tested compounds are dimethyldistearylammonium chloride (DSDMAC), cetyltrimethylammonium bromide (HTMAB) and cetylbenzyldimethylammonium chloride (HBDMAC). The results indicate DSDMAC is less toxic than the other two surfactants and that it biodegrades rapidly at both lower (2.5 mg/L) and higher (10 mg/L) concentrations.     

Denitrification in a Deep Basalt Aquifer: Implications for Aquifer Storage and Recovery

Aquifer storage and recovery (ASR) can provide a means of storing water for irrigation in agricultural areas where water availability is limited. A concern, however, is that the injected water may lead to a degradation of groundwater quality. In many agricultural areas, nitrate is a limiting factor. In the Umatilla Basin in north central Oregon, shallow alluvial groundwater with elevated nitrate‐nitrogen of <3 mg/L to >9 mg/L is injected into the Columbia River Basalt Group (CRBG), a transmissive confined aquifer(s) with low natural recharge rates. Once recovery of the injected water begins, however, NO₃‐N in the recovered water decreases quickly to <3 mg/L (Eaton et al. 2009), suggesting that NO₃‐N may not persist within the CRBG during ASR storage. In contrast to NO₃‐N, other constituents in the recovered water show little variation, inconsistent with migration or simple mixing as an explanation of the NO₃‐N decrease. Nitrogen isotopic ratios (δ¹⁵N) increase markedly, ranging from +3.5 to > +50, and correlate inversely with NO₃‐N concentrations. This variation occurs in <3 weeks and recovery of <10% of the originally injected volume. TOC is low in the basalt aquifer, averaging <1.5 mg/L, but high in the injected source water, averaging >3.0 mg/L. Similar to nitrate concentrations, TOC drops in the recovered water, consistent with this component contributing to the denitrification of nitrate during storage.     

Relating nitrogen sources and aquifer susceptibility to nitrate in shallow ground waters of the United States

Characteristics of nitrogen loading and aquifer susceptibility to contamination were evaluated to determine their influence on contamination of shallow ground water by nitrate. A set of 13 explanatory variables was derived from these characteristics, and variables that have a significant influence were identified using logistic regression (LR). Multivariate LR models based on more than 900 sampled wells predicted the probability of exceeding 4 mg/L of nitrate in ground water. The final LR model consists of the following variables: (1) nitrogen fertilizer loading (p-value = 0.012); (2) percent cropland-pasture (p < 0.001); (3) natural log of population density (p < 0.001); (4) percent well-drained soils (p = 0.002); (5) depth to the seasonally high water table (p = 0.001); and (6) presence or absence of a fracture zone within an aquifer (p = 0.002). Variables 1-3 were compiled within circular, 500 m radius areas surrounding sampled wells, and variables 4-6 were compiled within larger areas representing targeted land use and aquifers of interest. Fitting criteria indicate that the full logistic-regression model is highly significant (p < 0.001), compared with an intercept-only model that contains none of the explanatory variables. A goodness-of-fit test indicates that the model fits the data well, and observed and predicted probabilities of exceeding 4 mg/L nitrate in ground water are strongly correlated (r2 = 0.971). Based on the multivariate LR model, vulnerability of ground water to contamination by nitrate depends not on any single factor but on the combined, simultaneous influence of factors representing nitrogen loading sources and aquifer susceptibility characteristics.     

Water quality assessment for sustainable agriculture in the Wet Tropics--a community-assisted approach

A number of studies in north Queensland over the past two decades have concluded that large amounts of nutrients and sediments are exported from agricultural watersheds, particularly during wet season rainfall events. With the co-operation of a number of growers, runoff from Queensland Wet Tropics banana and cane farm paddocks in two distinct tropical river catchments was examined to provide an estimate of nutrient and sediment concentrations and export, with comparison to water quality of flow through a small urban lakes system. Median total nitrogen concentrations in cane drainage runoff (3110 microg N/L) were higher than for banana paddock drainage (2580 microg N/L), although the maximum concentration was recorded from a banana paddock (20,900 microg N/L). Nitrogen losses during post-event drainage flow were supplemented by high proportions of NO(X) (nitrate + nitrite) sourced from groundwater inputs. Banana paddocks had the highest maximum and median total phosphorus and TSS concentrations (5120 and 286 microg P/L, and 7250 and 75 mg/L respectively) compared to the cane farms (1430 and 50 microg P/L, and 1840 and 14 mg/L respectively). The higher phosphorus and TSS concentrations in the banana runoff were attributed to higher paddock slopes and a greater proportion of exposed ground surface during the wet season. Highest nutrient and TSS concentrations corresponded with samples collected near the peak discharge periods; however, the rising stage of the drainage flows, where the highest nutrient and TSS concentrations are often reported, were difficult to target because of the manual sampling strategy used. This study shows that high concentrations of nutrients and TSS occur in the runoff from cane and banana paddocks. Median total nitrogen, total phosphorus and TSS concentrations in flow through the urban lakes were 369 microg N/L, 16 microg P/L and 11 mg/L, respectively. Flux estimates of 9.2 kg N, 0.8 kg P and 126 kg TSS/ha were determined for drainage runoff from a banana paddock during a single intensive storm event.     

Estimating Aquifer Sensitivity to Nitrate Contamination Using Geochemical Information

Methods for predicting aquifer sensitivity to contamination typically ignore geochemical factors that affect the occurrence of contaminants such as nitrate. Use of geochemical information offers a simple and accurate method for estimating aquifer sensitivity to nitrate contamination. We developed a classification method in which nitrate-sensitive aquifers have dissolved oxygen concentrations > 1.0 mg/L, Eh values >250 mV, and either reduced iron concentrations < 0.1 mg/L or total iron concentrations < 0.7 mg/L. We tested the method in four Minnesota aquifer systems having different geochemical and hydrologic conditions. A surficial sand aquifer in central Minnesota exhibited geochemical zonation, with a rapid shift from aerobic to anaerobic conditions 5 m below the water table. A fractured bedrock aquifer in east-central Minnesota remained aerobic to depths of 50 m, except in areas where anaerobic ground water discharged upward from an underlying aquifer. A bedrock aquifer in southeast Minnesota exhibited aerobic conditions when overlain by surficial deposits lacking shale, whereas anaerobic conditions occurred under deposits that contained shale. Surficial sand aquifers in northwest Minnesota contained high concentrations of sulfate and were anaerobic throughout their extent. Nitrate-nitrogen was detected at concentrations exceeding 1 mg/L in 135 of 149 samples classified as sensitive. Nitrate was not detected in any of the 109 samples classified as not sensitive. We observed differences between our estimates of sensitivity and existing sensitivity maps, which are based on methods that do not consider aquifer geochemistry. Because dissolved oxygen, reduced iron, and Eh are readily measured in the field, use of geochemistry provides a quick and accurate way of assessing aquifer sensitivity to nitrate contamination.     

Contamination of the Sandstone Aquifer of Prince Edward Island, Canada by Aldicarb and Nitrogen Residues

Prince Edward Island is wholly dependent upon ground water from a highly permeable fractured sandstone aquifer for all industrial, domestic, agricultural, and potable uses. The contamination of this aquifer by agricultural residues, principally aldicarb and nitrate, has caused concern among Islanders. Ground water quality was monitored between 1985 and 1988 beneath two potato fields to which aldicarb (Temik) was applied at planting once or twice between 1983 and 1986. In May of 1988,12 percent of 48 monitoring well samples exceeded the drinking water guideline of 9μg/L for total aldicarb. Furthermore 32 percent of all samples exceeded the nitrate guideline of 10 mg/L. Aldicarb persistence appears related to its application at planting when soil temperatures are low and recharge is high and to the inhibiting pH effect that ammonium (from fertilizers and soil organic nitrogen) oxidation has on its degradation. Therefore, based on the research of others, it is recommended that aldicarb be applied at plant emergence when degradation is more rapid and recharge is lower.