DISSIPATION OF 2,4-D DMA AND BEE FROM WATER,MUD, AND FISH AT LAKE SEMINOLE,GEORGIA1

ABSTRACT: Four 10-ha plots in dense watermilfoil beds of Lake Seminole, Georgia, were each treated with either 2,4-D DMA or 2,4-D BEE at rates of 22.5 and 45 kg a.e./ha. Both formulations were shown to be rapidly converted to the 2,4-D acid form, with no detection of 2,4-D DMA or 2,4-D BEE in the water within less than 24 hours after treatment. The maximum detected 2,4-D concentrations in the high rate 2,4-D DMA and 2,4-D BEE plots were 3.6 and 0.68 mg/, respectively. However, all but seven samples at a 2,4-D BEE plot showed nondetectable herbicide levels by day 7, with all water samples showing nondetectable levels by day 13. Dimethylnitrosamine and 2,4-dichlorophenol, potentially toxic transformation products of the herbicide formulations, were at nondetectable levels in all water samples. Sediment samples showed no significant net accumulation of 2,4-D, 2,4-D BEE, or 2,4-dichlorophenol during the summer monitoring; dimethylnitrosamine remained at nondetectable levels. There was no accumulation of 2,4-D in fish collected from the two plots treated with 2,4-D DMA. Four of 24 game fish from the 2,4-D BEE treatment plots contained low levels of 2,4-D in muscle tissue, with a maximum value of 0.29 μg/g. In contrast, 18 of 20 gizzard shad collected from these plots through day 13 contained detectable 2,4-D in the muscle, with a maximum concentration of 6.9 μg/g. All fish collected after day 13 contained nondetectable levels of 2,4-D. Small decreases in dissolved oxygen and pH, associated with the complete watermilfoil control in all plots, had returned to normal summer values by day 28.     

HERBICIDES AND TRANSFORMATION PRODUCTS IN SURFACE WATERS OF THE MIDWESTERN UNITED STATES1

ABSTRACT: Most herbicides applied to crops are adsorbed by plants or transformed (degraded) in the soil, but small fractions are lost from fields and either move to streams in overland runoff, near surface flow, or subsurface drains, or they infiltrate slowly to ground water. Herbicide transformation products (TPs) can be more or less mobile and more or less toxic in the environment than their source herbicides. To obtain information on the concentrations of selected herbicides and TPs in surface waters of the Midwestern United States, 151 water samples were collected from 71 streams and five reservoir outflows in 1998. These samples were analyzed for 13 herbicides and 10 herbicide TPs. Herbicide TPs were found to occur as frequently or more frequently than source herbicides and at concentrations that were often larger than their source herbicides. Most samples contained a mixture of more than 10 different herbicides or TPs. The ratios of TPs to herbicide concentrations can be used to determine the source of herbicides in streams. Results of a two‐component mixing model suggest that on average 90 percent or more of the herbicide mass in Midwestern streams during early summer runoff events originates from the runoff and 10 percent or less comes from increased ground water discharge.     

EFFECTS OF SELECTED HERBICIDES ON BACTERIAL POPULATIONS IN NONTREATED AND TREATED WATER1

ABSTRACT: Bacterial populations in nontreated and herbicide-treated waters were subjected to three different herbicides. Diuron, dichlobenil, and diquat were added (100 mg/l) to water samples from two fresh water lakes and two herbicide-treated ponds. Total numbers of bacteria were monitored. Bacterial populations in fresh lake water decreased after herbicide additions; however, final populations were significantly greater than the controls. Similar observations were recorded for bacteria in dichlobenil- and diuron-treated waters. Selective enrichment is probably expressed in these experiments.     

Seasonal variation of herbicide concentrations in prairie farm dugouts

Prairie farm dugouts are frequently constructed for use as potable water sources. Consequently, cumulative pesticide inputs via atmospheric deposition and surface runoff may constitute a risk to human health. Since, relative to other pesticides, herbicides are used in greatest amount on the Canadian prairies, herbicide concentrations were intensively monitored in three dugouts over three growing seasons. Herbicides were detected in the water of all three dugouts each growing season which may reflect cumulative inputs from atmospheric and surface processes over the lifetimes of the dugouts, which varied from 11 to 22 yr. Detections, which were not continuous, tended to be seasonal in nature. During the 3-yr study, detections were most frequent during the spring application period and late fall following dugout turnover. Between these periods, herbicide concentrations generally decreased to below detection limits. The reappearance of herbicides in the dugout water during fall turnover and in concentrations generally greater than those present during the spring application period suggest that, under appropriate environmental conditions, the bottom sediments may act as a source of herbicides to the water column. In general, herbicide inputs due to deposition of application drift did not result in detectable concentrations of herbicides in the dugouts. In the only year that winter samples were monitored, herbicides were also detected during ice cover. On the basis of monthly sampling over each growing season, median concentrations of 9 of the 10 herbicides monitored were less than 0.05 microg L(-1). The exception, 2,4-D, which has been used extensively on the Canadian prairies for more than 50 yr and in greatest amounts, was the most frequently detected herbicide. In no case did herbicide concentrations exceed Canadian drinking water guidelines; however, on occasion maximum herbicide concentrations did exceed aquatic life and irrigation water guidelines.     

HERBICIDES AND DEGRADATES IN SHALLOW AQUIFERS OF ILLINOIS: SPATIAL AND TEMPORAL TRENDS1

ABSTRACT: During the fall of 2000, the occurrence was examined of 16 herbicides and 13 herbicide degradates in samples from 55 wells in shallow aquifers underlying grain producing regions of Illinois. Herbicide compounds with concentrations above 0.05 μg/L were detected in 56 percent of the samples. No concentrations exceeded regulatory drinking water standards. The six most frequently detected compounds were degradates. Water age was an important factor in determining vulnerability of ground water to transport of herbicide compounds. Unconsolidated aquifers, which were indicated to generally contain younger ground water than bedrock aquifers, had a higher occurrence of herbicides (73 percent of samples) than bedrock aquifers (22 percent). Temporal analysis to determine if changes in concentrations of selected herbicides and degradates could be observed over a near decadal period indicated a decrease in detection frequency (25 to 18 percent) between samplings in 1991 and 2000. Over this period, significant differences in concentrations were observed for atrazine (decrease) and total acetochlor (increase). The increase in acetochlor compound concentrations corresponds to an increase in acetochlor use during the study period, while the decrease in atrazine concentrations corresponds to relatively consistent use of atrazine. Changes in frequency of herbicide detection and concentration do not appear related to changes in land use near sampled wells.     

REGRESSION MODELS OF HERBICIDE CONCENTRATIONS IN OUTFLOW FROM RESERVOIRS IN THE MIDWESTERN USA, 1992–19931

ABSTRACT: Reservoirs are used to store water for public water supply, flood control, irrigation, recreation, hydropower, and wildlife habitat, but also often store undesirable substances such as herbicides. The outflow from 76 reservoirs in the midwestern USA, was sampled four times in 1992 and four times in 1993. At least one herbicide was detected in 82.6 percent of all samples, and atrazine was detected in 82.1 percent of all samples. Herbicide properties; topography, land use, herbicide use, and soil type in the contributing drainage area; residence time of water in reservoirs; and timing of inflow, release, and rainfall all can affect the concentration of herbicides in reservoirs. A GIS was used to quantify characteristics of land use, agricultural chemical use, climatic conditions, topographic character, and soil type by reservoir drainage basins. Multiple linear and logistic regression equations were used to model mean herbicide concentrations in reservoir outflow as a function of these characteristics. Results demonstrate a strong association between mean herbicide concentrations in reservoir outflow and herbicide use rates within associated drainage basins. Results also demonstrate the importance of including soils and basin hydrologic characteristics in models used to estimate mean herbicide concentrations.     

PERCOLATE WATER AND BROMIDE MOVEMENT IN THE ROOT ZONE OF EFFLUENT IRRIGATION SITES1

ABSTRACT: A bromide tracer was used to evaluate percolate water and ion movement in the upper 1.2 m of soil at a proposed sewage effluent irrigation site located in the Missouri Ozarks. Two plots representing Doniphan silt loam and Crider silt loam soils were sprinkler irrigated with local ground water at a rate of 7.62 cm/week from June through August 1976. Soil water potential, percent soil moisture by volume, and background levels of bromide in soil water, ground water, and precipitation were measured at the study plots. Bromide exchange properties and saturated hydraulic conductivity of the soils were determined in the laboratory. During two selected time periods, irrigation water, was spiked with NaBr (5.0 mg/l Br). Bromide movement through the upper profile was quantified by soil water samples and post-sampling neutron activation analysis. Soil moisture was near saturatin in both soils when the Br tracer was applied. Bromide concentrations above background levels (0.023 mg/l Br, Doniphan silt loam and 0.016 mg/l Br, Crider silt loam) were detected within 2.60 hours at 0.9 m in the Doniphan soil and within 3.75 hours at that depth in the Crider soil. The rate of Br movement in the profile was greater in both soils than the measured saturated hydraulic conductivity, Bromide concentrations above background levels were present in soil water from the study plots for a minimum of 21 days after irrigation with the Br tracer.     

无机高分子絮凝剂聚合氯化铁的制备与应用

综述了分别以氯化铁、硫铁矿烧渣和酸洗废液为原料制备无机高分子絮凝剂聚合氯化铁的方法，以及其在低浊度水、合成洗涤剂废水和印染废水等水处理方面的应用。指出了聚合氯化铁絮凝剂在制备及应用上的发展趋势。     

PHOSPHORUS LOSSES FROM CROPLAND AS AFFECTED BY TILLAGE SYSTEM AND FERTILIZER APPLICATION METHOD1

ABSTRACT: A rainfall simulator was used to study the effectiveness of no-till and fertilizer application method on reducing phosphorus (P) losses from agricultural lands. Simulated rainfall was applied to 12 experimental field plots, each 0.01 ha in size. The plots were divided into no-till and conventional tillage systems. Two fertilizer application methods, subsurface injection and surface application, were investigated for the two tillage systems. Phosphorus fertilizer was applied at a rate of 46 kg/ha, 24 to 48 hours before the start of rain simulation. Water samples were collected from the base of each plot and analyzed for sediment and P content. No-till was found to be very effective in reducing runoff and sediment losses. No-till reduced sediment loss and total runoff volume by 92 and 67 percent, respectively. Subsurface injection of fertilizer, as compared to surface application, reduced PO₄ losses by 39 percent for no-till and by 35 percent for conventional tillage. The effect of tillage system on PO₄ losses was not significant. Reductions in total-P (P_T) losses due to no-till compared to the conventional tillage system were 89 and 91 percent for surface application and subsurface injection methods, respectively. Averaged across all fertilizer treatments, an equivalent of 0.9 and 8.9 percent of the P applied to the plots were lost from the no-till and conventional tillage plots, respectively.     

Removal of an anionic dye (Acid Blue 92) by coagulation–flocculation using chitosan

Chitosan (a biopolymer) is an aminopolysaccharide that can be used for the treatment of colored solutions by coagulation–flocculation (as an alternative to more conventional processes such as sorption). Acid Blue 92 (a sulfonic dye) was selected as a model dye for verifying chitosan's ability to treat textile wastewater. A preliminary experiment demonstrated that chitosan was more efficient at color removal in tap water than in demineralized water, and that a substantially lower concentration of chitosan could be used with tap water. Dye removal reached up to 99% under optimum concentration; i.e., in terms of the acidic solutions and the stoichiometric ratio between the amine groups of the biopolymer and the sulfonic groups in the dye. The flocs were recovered and the dye was efficiently removed using alkaline solutions (0.001–1 M NaOH solutions) and the biopolymer, re-dissolved in acetic acid solution, was reused in a further treatment cycle.     

PESTICIDES AND PESTICIDE DEGRADATION PRODUCTS IN STORMWATER RUNOFF: SACRAMENTO RWER BASIN,CALIFORNIA1

ABSTRACT: Pesticides in stormwater runoff, within the Sacramento River Basin, California, were assessed during a storm that occurred in January 1994. Two organophosphate insecticides (diazinon and methidathion), two carbamate pesticides (molinate and carbofuran), and one triazine herbicide (simazine) were detected. Organophosphate pesticide concentrations increased with the rising stage of the hydrographs; peak concentrations were measured near peak discharge. Diazinon oxon, a toxic degradation product of diazinon, made up approximately 1 to 3 percent of the diazinon load. The Feather River was the principal source of organophosphate pesticides to the Sacramento River during this storm. The concentrations of molinate and carbofuran, pesticides applied to rice fields during May and June, were relatively constant during and after the storm. Their presence in surface water was attributed to the flooding and subsequent drainage, as a management practice to degrade rice stubble prior to the next planting. A photo-degradation product of molinate, 4-keto molinate, was in all samples where molinate was detected and made up approximately 50 percent of the total molinate load. Simazine, a herbicide used in orchards and to control weeds along the roadways, was detected in the storm runoff, but it was not possible to differentiate the two sources of that pesticide to the Sacramento River.     

Atrazine and alachlor transport in claypan soils as influenced by differential antecedent soil water content

Increased attention to ground water contamination has encouraged an interest in mechanisms of solute transport through soils. Few studies have investigated the effect of the initial soil water content on the transport and degradation of herbicides for claypan soils. We investigated the effect of claypan soils at initial field capacity vs. permanent wilting level on atrazine and alachlor transport. The soil studied was Mexico silt loam (fine, smectitic, mesic Aeric Vertic Epiaqualf) with a subsoil clay content, primarily montmorillonite, of >40%. Strontium bromide, atrazine, and alachlor were applied to plots; half were at field capacity (Wet treatment), and half were near the permanent wilting point (Dry treatment). Soil cores were removed at selected depths and times, and cores were analyzed for bromide and herbicide concentrations. Bromide, atrazine, and alachlor were detected at the 0.90-m depth in dry plots within 15 d after experiment initiation. Bromide was detected 0.15 m deeper (P < 0.05) in the Dry compared with the Wet treatment at 1, 7, and 60 d after application and >0.30 m deeper (P < 0.01) in the Dry treatment at 15 and 30 d after application; similar treatment results were found for atrazine and alachlor, although on fewer dates with significant differences. The mobility order of the applied chemicals was bromide > atrazine > alachlor. The atrazine apparent half-life was significantly longer in the Dry plots compared with the Wet plots. The retardation factor determined from the relative velocity of each herbicide to that of bromide was higher for alachlor than for atrazine. This study identifies the impact that shrinkage cracks have for different moisture conditions on preferential transport of herbicides in claypan soils.     

NUTRIENT AND β17‐ESTRADIOL LOSS IN RUNOFF WATER FROM POULTRY LITTERS1

ABSTRACT: A main water quality concern is accelerated eutrophication of fresh waters from nonpoint source pollution, particularly nutrient transport in surface runoff from agricultural areas and confined animal feeding operations. This study examined nutrient and β₁₇‐estradiol concentrations in runoff from small plots where six poultry litters were applied at a rate of about 67 kg/ha of total phosphorus (TP). The six poultry litter treatments included pelleted compost, pelleted litter, raw litter, alum (treated) litter, pelleted alum litter, and normal litter (no alum). Four replicates of the six poultry litter treatments and a control (plots without poultry litter application) were used in this study. Rainfall simulations at intensity of 50 mm/hr were conducted immediately following poultry litter application to the plots and again 30 days later. Composite runoff samples were analyzed for soluble reactive phosphorus (SRP), ammonia (NH₄), nitrate (NO₃), TP, total nitrogen (TN) and β₁₇‐estradiol concentrations. In general, poultry litter applications increased nutrient and β₁₇‐estradiol concentrations in runoff water. Ammonia and P concentrations in runoff water from the first simulation were correlated to application rates of water extractable NH₄ (R²= 0.70) and P (R²= 0.68) in the manure. Results suggest that alum applications to poultry litter in houses in between flocks is an effective best management practice for reducing phosphorus (P) and β₁₇‐estradiol concentrations in runoff and that pelleted poultry litters may increase the potential for P and β₁₇‐estradiol loss in runoff water. Inferences regarding pelleted poultry litters should be viewed cautiously, because the environmental consequence of pelleting poultry litters needs additional investigation.     

Leaching of three imidazolinone herbicides during sprinkler irrigation

Some imidazolinone herbicides have been shown to be mobile in soil, raising concern about their possible movement to ground water. Three imidazolinone herbicides (imazamethabenz-methyl, 497 g ha(-1); imazethapyr, 14.7 g ha(-1); and imazamox, 14.7 g ha(-1)) commonly used in crop production on the Canadian prairies were applied to a tile-drained field to assess their susceptibility to leach when subjected to sprinkler irrigation using a center pivot. Tile-drain flow began when the water table rose above tile-drain depth, and peak flow rates corresponded to the greatest depths of ground water above the tile drains. Interception of irrigation water by the tile drains in each quadrant of the field varied from ～11 to 20% of the water applied. Under a worst-case scenario in which irrigation began the day after herbicide application and irrigation water was applied at 25 mm d(-1) for 12 d, there was evidence of preferential flow of all three herbicides and hydrolysis of imazamethabenz-methyl to imazamethabenz in the initial samples of tile-drain effluent. In subsequent samples, concentrations (analysis by LC-MS-MS) of the summation of imazamethabenz-methyl (25-24,000 ng L(-1)) plus its hydrolysis product imazamethabenz (63-26,500 ng L(-1)) greatly exceeded those of imazethapyr (<13-1260 ng L) and imazamox (19-599 ng L(-1)), thus reflecting relative application rates. In contrast, estimates of total transport of each herbicide from the root zone, which varied in each quadrant and ranged from 0.06 to 2.3% for imazamethabenz-methyl plus imazamethabenz, 0.71 to 3.1% for imazethapyr, and 0.61 to 2.8% for imazamox, did not reflect application rates. In shallow ground water (piezometer samples), there was inconsistent and infrequent detection all four compounds. With the frequency and amount of rainfall typically encountered in the prairie region of Canada, contamination of shallow ground water with detectable concentrations of the three imidazolinone herbicides would be unlikely.     

REAL-TIME MANAGEMENT OF WATER QUALITY IN THE SAN JOAQUIN RWER BASIN,CALIFORNIA1

ABSTRACT: In the San Joaquin River Basin, California, a realtime water quality forecasting model was developed to help improve the management of saline agricultural and wetland drainage to meet water quality objectives. Predicted salt loads from the water quality forecasting model, SJRIODAY, were consistently within ± 11 percent of actual, within ± 14 percent for seven-day forecasts, and within ± 26 percent for 14-day forecasts for the 16- month trial period. When the 48 days dominated by rainfall/runoff events were eliminated from the data set, the error bar decreased to ± 9 percent for the model and ± 11 percent and ± 17 percent for the seven-day and 14-day forecasts, respectively. Constraints on the use of the model for salinity management on the San Joaquin River include the number of entities that control or influence water quality and the lack of a centralized authority to direct their activities. The lack of real-time monitoring sensors for other primary constituents of concern, such as selenium and boron, limits the application of the model to salinity at the present time. A case study describes wetland drainage releases scheduled to coincide with high river flows and significant river assimilative capacity for salt loads.     

ARSENIC CONSUMPTION AND HEALTH RISK PERCEPTIONS IN A RURAL WESTERN U.S. AREA1

ABSTRACT: Churchill County, Nevada, has approximately 23,000 residents, among whom an estimated 13,500 relied on private wells for water supply in 2002. This study examined exposure to arsenic in water supplies among residents with private domestic wells and factors related to householder choice to consume tap water. It compared opinions and concerns about water quality with consumption habits and observed concentrations from tap water samples. The results from 351 households indicated that a majority (75 percent) of respondents consumed tap water and that a minority (38 percent) applied treatment. Approximately 66 percent of those who consumed tap water were exposed to concentrations of arsenic that exceeded 10 ppb. Water consumption was related to application of treatment. Among 98 respondents who were not at all concerned about the health effects of aqueous arsenic, 59 (60 percent) reported consuming tap water with concentrations of arsenic exceeding 10 ppb. Conversely, among 86 respondents who were highly concerned about arsenic, 33 (37 percent) consumed tap water with concentrations of arsenic exceeding 10 ppb. Results from a national sampling effort showed that 620 of 5,304 private wells sampled (11.7 percent) had arsenic concentrations above 10 ppb. The paradox of awareness of arsenic in water supplies coupled with consumption of aqueous arsenic in concentrations greater than 10 ppb may be common in other parts of the nation. Enhanced educational efforts, especially related to tap water sampling and explanations of efficacy of available treatment, may be useful means of reducing exposure through private water supplies.     

REGRESSION MODELS FOR ESTIMATING HERBICIDE CONCENTRATIONS IN U.S. STREAMS FROM WATERSHED CHARACTERISTICS1

ABSTRACT: Regression models were developed for estimating stream concentrations of the herbicides alachlor, atrazine, cyanazine, metolachior, and trilluralin from use‐intensity data and watershed characteristics. Concentrations were determined from samples collected from 45 streams throughout the United States during 1993 to 1995 as part of the U.S. Geological Survey's National Water‐Quality Assessment (NAWQA). Separate regression models were developed for each of six percentiles (10th, 25th, 50th, 75th, 90th, 95th) of the annual distribution of stream concentrations and for the annual time‐weighted mean concentration. Estimates for the individual percentiles can be combined to provide an estimate of the annual distribution of concentrations for a given stream. Agricultural use of the herbicide in the watershed was a significant predictor in nearly all of the models. Several hydrologic and soil parameters also were useful in explaining the variability in concentrations of herbicides among the streams. Most of the regression models developed for estimation of concentration percentiles and annual mean concentrations accounted for 50 percent to 90 percent of the variability among streams. Predicted concentrations were nearly always within an order of magnitude of the measured concentrations for the model‐development streams, and predicted concentration distributions reasonably matched the actual distributions in most cases. Results from application of the models to streams not included in the model development data set are encouraging, but further validation of the regression approach described in this paper is needed.     

Fate of polydimethylsilicone in biosolids-amended field plots

This research examined the fate of polydimethylsilicones (PDMS) in agricultural test plots amended with municipal biosolids. This 4 yr field study involved addition of 0, 15, and 100 Mg ha(-1) of municipal biosolids, which contained ambient concentrations of PDMS (1272 mg kg(-1) biosolids), to corn and soybean test plots. Soil samples collected at intermittent time intervals were analyzed for soil water, soil organic C, extractable PDMS and PDMS hydrolysis products. Above normal precipitation during the field study maintained soil water levels in excess of 100 g kg(-1) for most of the testing period of 1994-1998. Under these conditions half-lives for PDMS (based on field dissipation data) ranged from 876 to 1443 d. When biosolids amended soil samples were brought into the laboratory and subjected to more rapid drying, >80% of the PDMS was transformed to lower molecular weight hydrolysis products within 20 d. No difference in relative PDMS transformation rates were evident for soils that received PDMS in the form of a biosolids amendment or directly dosed to the soil (in the absence of biosolids) indicating little if any effect of direct PDMS-biosolids interactions on PDMS transformation rates. These results support that the overriding factor controlling the fate of PDMS in field soils is the soil moisture content.     

地面水中叶枯灵的高效液相色谱测定

本文采用反相高效液相色谱法，在质控条件下，对河水，塘水两种地面水中叶枯灵的检验方法进行了测试，用Shimapck ODS柱为分析柱，以甲醇：水＝50：50为流动相，并用冰醋酸调PH至4－5，紫外检测波长281nm，两种水样的平均回收率分别为91．7－96．3％，90－95．8％，相对标准偏差为4．3％，最低检出限为0．0261mg/l，为地面水中叶枯灵卫生标准的实施提供了简便，灵敏，正确的配套测试手段。     

EFFECT OF SULFOMETURON METHYL ON GROUND WATER AND STREAM QUALITY IN COASTAL PLAIN FOREST WATERSHEDS1

ABSTRACT: Sulfometuron methyl [methyl 2-[[[[4,6-dimethly 2-(pyrimidinyl) a-mino] carbony l]amino] sulfonyl] benzoate] was applied by a ground sprayer at a maximum labeled rate of 0.42 kg ha^-1 a.i. to a 4 ha Coastal Plain flatwoods watershed as site preparation for tree planting. Herbicide residues were detected in Streamflow for only seven days after treatment and did not exceed 7 mg m^-3. Sulfometuron methyl was not detected in any stormflow and was not found in any sediment (both bedload and suspended). Sampling of a shallow ground water aquifer, > 1.5 m below ground surface, did not detect any sulfometuron methyl residues for 203 days after herbicide application. Lack of herbicide residue movement was attributed to low application rates, rapid hydrolysis in acidic soils and water and dilution in streamflow.