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1.
Pesticide movement to subsurface drains was monitored in two typical crop production areas in Germany. Field trials were conducted on two subsurfacedrained soils, a silt loam and a poorly structured sandy soil, under different climatic conditions. Over a period of one year, the drainflow was measured and the drain water was analysed for all applied herbicides. Different leaching behaviour was observed at the two field sites. Following autumn application of pendimethalin and isoproturon to the Soester Börde soil, maximum concentrations of about 62 μg litre?1 for isoproturon and 0.7 μg litre?1 for pendimethalin were observed in drainflow from this silt loam. The early occurrence of both herbicides in the drain water only two days after application is consistent with fast flow through macropores. In contrast, on the subsurfacedrained sandy soil in Brandenburg, isoproturon did not reach the drains until two months after autumn application and was found at maximum concentrations of only 1.4 μg litre?1; pendimethalin was not detected in the drain water. Pesticide movement after spring application seemed to be of minor importance. At both locations, spring application led to low concentrations of pesticides in the drainflow (pendimethalin < 0.01 μ litre?1; metolachlor ? 0.05 μ litre?1; chloridazon ? 0.15 μ litre?1; metamitron ? 0.02 μg litre?1; terbuthylazine ? 1.4 μ litre?1).  相似文献   

2.
A method is described for the analysis of the herbicide bromoxynil and its octanoate in soils. Following extraction with aqueous acidic acetonitrile, the octanoate was separated from the phenolic bromoxynil by solvent partitioning. The ester and the phenol were assayed by gas-liquid chromatography without further modification or preparation of a derivative. Recoveries in excess of 93% were obtained from soils treated with the phenol and the ester at levels of 0.5 or 0.1 μg g?1. The persistence of bromoxynil octanoate applied at a rate of 3 μg g?1 was studied in the laboratory on a heavy clay and a sandy loam at 85% of field capacity moisture and 20°1°C, both alone and in the presence of 2,4-D (2 μg g?1); MCPA (2 μg g?1); MCPA+asulam (both at 2 μg g?1); and MCPA+difenzoquat (both at 2 μg g?1). In each soil there was a rapid conversion of bromoxynil octanoate to the free phenol, which then underwent a rapid degradation, so that after 7 days, over 90% of the original treatment had disappeared. There appeared to be no effect on bromoxynil breakdown by any of the herbicides added in combination. Small field plots were treated, in early May 1977 and 1978 at two locations in Saskatchewan, with a combination of commercial formulations containing asulam, bromoxynil octanoate, and MCPA at rates of 1 kg ha?1 each. After 10 weeks the plots were sampled and analysis showed that in all cases, no asulam, bromoxynil, or bromoxynil octanoate could be extracted from the top 10 cm of soil.  相似文献   

3.
A CIPAC/AOAC test with tomato plants is used to specify the volatility ratings of herbicide ester formulations. This work compares the tomato plant test with an alternative chemical one. The concentrations of esters and the effective molecular weight and density of each formulation were used with the ester vapour pressures to calculate its herbicide vapour pressure as complete, and evaporated formulations. The range was from 28.8 mPa (at 257deg;C) for a mixture of 2,4–D esters to 0–07 mPa (at 25°C) for a 2,4,5–T-(iso-octyl) formulation, as complete formulations, and 35-5 and 0–16 mPa (at 25°C) as evaporated ones. A value of 0–6 mPa (at 25°C) was selected on the basis of the tomato plant test as the cut-off area for low-volatile esters and is recommended to be included in specifications for herbicide esters. Formulations with a herbicide vapour pressure above 3.3 mPa (at 25°C) are high-volatile ones according to the tomato plant test, while between 0–6–3.3 mPa (at 25°C) is a borderline region where the test gives mixed results. Levels of 2,4–D-ethyl and methyl were added to pure 2–ethylhexyl esters of 2,4–D and a 2,4,5–T-(iso-octyl) formulation to find what level of contamination would change the rating of these esters from low to high volatile. Formulations of 2,4–D-(iso-octyl) should not contain more than 11 g litre?1 2,4–D as methyl ester or 2.0 g litre?1 2,4–D as ethyl ester. Formulations of 2,4,5–T-(iso-octyl) should not contain more than 26 g litre?1 2,4–D as methyl ester or 4.7g litre?1 2,4–D as ethyl ester.  相似文献   

4.
Enzyme immunoassay (EIA) has been tested for the detection of atrazine in soil and water. EIA kits and atrazine-fortified samples were received from the International Atomic Energy Agency. Atrazine concentrations of about 0·01 μg litre-1 could be detected and the central detection point was found at about 0·15 μg litre-1 which is a reasonably sensitive region for atrazine. A validation study with spiked local water samples yielded acceptable results. No treatment was required for water samples. Extraction of atrazine from soil was done by simple shaking with methanol without any clean-up steps. Detection limits of 1×10-2 μg litre-1 for water and 5×10-3 μg kg-1 for soil were achieved. © 1998 SCI.  相似文献   

5.
A method is described for the analysis of small amounts of hydrazine in maleic hydrazide formulations. Following derivative formation with pentafluorobenz-aldehyde, the pentafluorobenzaldehyde azine was extracted with hexane and determined by gas-liquid chromatography with electron-capture detection. Recoveries of 72-80% were obtained from samples fortified with 1 and 10 μg of hydrazine. The limit of detection was 0.05 mg kg?1. Fourteen commercial formulations with maleic hydrazide concentrations ranging from 180-360 g litre?1 were investigated. The hydrazine content of the maleic hydrazide used in these formulations ranged from less than 0.05 to 53 mg kg?1. During the storage of two samples at 50°C for 10 weeks, the hydrazine contents increased from 2.2 to 124 and 0.4 to 54 mg litre?1, respectively.  相似文献   

6.
The effects of two herbicides, glyphosate (as a 359 g litre?1 SL) and hexazinone (as a 50gkg?1 granule) on soil microbial population, carbon dioxide evolution, and in-vitro growth of five species of ectomycorrhizal fungi were investigated. Glyphosate at 0–54 and 3.23 kg a.i. ha?1 and hexazinone at 1. 2 and 8 kg a.i. ha?1 did not reduce soil microbial population or carbon dioxide evolution in the long term (6 months). However, there was a significant short-term (2 months) effect of glyphosate on both fungal and bacterial counts at the 0.54 kg ha?1 treatment. In in-vitro tests, Cenococcum graniforme. Hebeloma crustuliniforme and Laccaria laccata were more susceptible to both herbicides than was Suillus tomentosus. which was, in turn, more susceptible than Paxillus involutus. The growth of all five ectomycorrhizal fungi was significantly reduced when subjected to concentrations above 50 μl formulation litre?1 (glyphosate) or 50 μg formulation litre?1 (hexazinone).  相似文献   

7.
Batch adsorption Koc values of fluroxypyr-methylheptyl ester (20000 1kg?1) and fluroxypyr (74 1kg?1) indicate increased mobility after hydrolysis of the ester to fluroxypyr. After 1 to 2 weeks incubation time in four soils, desorption Koc values of fluroxypyr were 100-200 1kg?1 but increased to 400-700 1kg?1 after 8 weeks. The increase in desorption Koc was related to incubation time and not to concentration, and it was interpreted as an entrapment of the fluroxypyr within the soil organic matter. Similar increases in desorption Koc with incubation time were noticed for pyridinol and methoxypyridine metabolites of fluroxypyr. Koc values also increased along the metabolic sequence fluroxypyr/pyridinol/methoxypyridine, with maximum Koc values of 3000-4000 1 kg?1 for the methoxypyridine metabolite. Hence mobility of the fluroxypyr aromatic ring strongly decreases with increased residence time in the soil.  相似文献   

8.
Structure-concentration–foliar uptake enhancement relationships between commercial polyoxyethylene primary aliphatic alcohol (A), nonylphenol (NP), primary aliphatic amine (AM) surfactants and the herbicide glyphosatemono(isopropylammonium) were studied in experiments with wheat (Triticum aestivum L.) and field bean (Vicia faba L.) plants growing under controlled-environment conditions. Candidate surfactants had mean molar ethylene oxide (EO) contents ranging from 5 to 20 and were added at concentrations varying from 0·2 to 10 g litre?-1 to [14C]glyphosate formulations in acetone–water. Rates and total amounts of herbicide uptake from c. 0·2–μl droplet applications of formulations to leaves were influenced by surfactant EO content, surfactant hydrophobe composition, surfactant concentration, glyphosate concentration and plant species, in a complex manner. Surfactant effects were most pronounced at 0·5 g acid equivalent (a.e.) glyphosate litre?-1 where, for both target species, surfactants of high EO content (15–20) were most effective at enhancing herbicide uptake: surfactants of lower EO content (5–10) frequently reduced, or failed to improve, glyphosate absorption. Whereas, at optimal EO content, AM surfactants caused greatest uptake enhancement on wheat, A surfactants gave the best overall performance on field bean; NP surfactants were generally the least efficient class of adjuvants on both species. Threshold concentrations of surfactants needed to increase glyphosate uptake were much higher in field bean than wheat (c. 2 g litre?-1 and < 1 g litre?-1, respectively); less herbicide was taken up by both species at high AM surfactant concentrations. At 5 and 10 g a.e. glyphosate litre?-1, there were substantial increases in herbicide absorption and surfactant addition could cause effects on uptake that were different from those observed at lower herbicide doses. In particular, the influence of EO content on glyphosate uptake was now much less marked in both species, especially with AM surfactants. The fundamental importance of glyphosate concentration for its uptake was further emphasised by experiments using formulations with constant a.i./surfactant weight ratios. Any increased foliar penetration resulting from inclusion of surfactants in 0·5 g litre?-1 [14C]glyphosate formulations gave concomitant increases in the amounts of radiolabel that were translocated away from the site of application. At these low herbicide doses, translocation of absorbed [14C]glyphosate in wheat was c. twice that in field bean; surfactant addition to the formulation did not increase the proportion transported in wheat but substantially enhanced it in field bean.  相似文献   

9.
The uncalibrated predictive ability of four preferential flow models (CRACK‐NP, MACRO/MACRO_DB, PLM, SWAT) has been evaluated against point rates of drainflow and associated concentrations of isoproturon from a highly structured and heterogeneous clay soil in the south of England. Data were available for four plots for a number of storm events in each of three successive growing seasons. The mechanistic models CRACK‐NP and MACRO generally gave reasonable estimates of drainflow over the three seasons, but under‐estimated concentrations of isoproturon over a prolonged period in the first season and over‐estimated them in the two remaining seasons. CRACK‐NP simulated maximum concentrations of isoproturon over the first two events of each of the three seasons of 156, 527 and 24.4 µg litre?1, respectively, and matched the observed data (465, 65.1 and 0.65 µg litre?1) slightly better than MACRO (69.1, 566 and 58.5 µg litre?1). Automatic selection of parameters from soils information within MACRO_DB reduced the emphasis on preferential flow relative to the stand‐alone version of MACRO. This gave a poor simulation of isoproturon breakthrough and simulated maximum concentrations were 0, 50.1 and 35.1 µg litre?1, respectively. The capacity model PLM gave the best overall simulation of total drainflow for the first two events in each season, but over‐estimated concentrations of isoproturon (967, 808 and 51.3 µg litre?1). The simple model SWAT represented total drainflow reasonably well and gave the best simulation of maximum isoproturon concentrations (140, 80.2 and 8.2 µg litre?1). There was no clear advantage here in using the mechanistic models rather than the simpler models. None of the models tested was able to simulate consistently the data set, and uncalibrated modelling cannot be recommended for such artificially drained heavy clay soils. © 2001 Society of Chemical Industry  相似文献   

10.
The content of the herbicides atrazine and hexazinone was measured in drainage water from seven to ten-year-old plantations grown with Abies nordmanniana (Steven) Spach on two clayey soils in Denmark. The concentrations of atrazine varied between 0.06 and 7.79 μg litre?1. The concentrations of hexazinone were different at the two locations, ranging from 0.07 to 2.09 μg litre?1 at Bremersvold and from 3.47 to 42.66 μg litre?1 at Koege. Metabolites of both herbicides were identified.  相似文献   

11.
The retention and degradation of metribuzin herbicide were studied under two environmental conditions. Field studies were carried out on two soils, a sandy loam soil (soil A) and a clay soil (soil B). Metribuzin was applied with a jet sprayer at 1060 g a.i. ha?1 and 1960 g a.i. ha?1 on soils A and B respectively. Reconstituted soil columns were used to study the herbicide movement and metabolism in the two soils. Analyses of metribuzin and its metabolites were carried out using standardized methods. The results indicated a very weak capacity of adsorption of metribuzin in the two soils, and the weak adsorbed fraction is easily desorbed. Degradation and mobility of metribuzin in the field and laboratory soil columns were very intense and rapid. Soil A favoured reductive deamination whereas soil B favoured oxidative desulphuration and the respective metabolites deaminometribuzin and diketometribuzin yield the same product deaminodiketometribuzin. Both leaching by rainfall and degradation were important in the disappearance of metribuzin from the soils.  相似文献   

12.
Fluroxypyr-MHE (methylheptyl ester) was applied to small field plots containing Londo sandy loam soil. After 30 days, fluroxypyr had degraded to about 60% of the initial concentration, but was still the main component, while after 120 and 366 days the methoxypyridine metabolite was the main component in the soil. At 30, 120, and 366 days, lettuce, turnips, green beans, soybeans, and wheat were planted and grown with no observed injury. Residues of 14C in the edible crop fractions were indistinguishable from 14C in control plants exposed to 14CO2, while residues in plant greens and chaff were low (0.1–0.2 mg kg?1), with little evidence of fluroxypyr and no evidence of metabolite uptake. These results indicate that the methoxypyridine metabolite, if present in the soil, does not harm and is not taken up into the plants.  相似文献   

13.
A field experiment was established to monitor preferential flow pathways and their capacity to transport isoproturon in a heavy clay soil. A hydrologically defined plot of 600 m2 at a field site on the Oxford University Farm at Wytham was created with integral flow monitoring and sampling devices. Data are presented from two flow events which occurred in April and May 1994. The highest concentrations of isoproturon (130 μg litre−1) were observed in the drainage system. The vast majority of the 0·7% of applied pesticide that left the plot was via the drainage system (75–90%) with lateral subsurface flow accounting for a smaller proportion (max 23%). Whilst high pesticide concentrations could be found in overland-flow water, the volumes of water moved by this route were small (max 3%). Less water was estimated to have left the field in response to rainfall than in the previous year. This was attributed to decay of the mole drain system. Consequently the amount of applied pesticide lost in runoff (0·7%) was less than that estimated for the first year (1·5%). The work has shown that, even when a farmer follows best practice in the application of a herbicide to a winter cereal in a drained clay field, high concentrations of the herbicide (relative to the EC drinking water limit) will contaminate surrounding watercourses.  相似文献   

14.
BACKGROUND: Pyrazosulfuron ethyl, a new rice herbicide belonging to the sulfonylurea group, has recently been registered in India for weed control in rice crops. Many field experiments revealed the bioefficacy of this herbicide; however, no information is available on the persistence of this herbicide in paddy soil under Indian tropical conditions. Therefore, a field experiment was undertaken to investigate the fate of pyrazosulfuron ethyl in soil and water of rice fields. Persistence studies were also carried out under laboratory conditions in sterile and non‐sterile soil to evaluate the microbial contribution to degradation. RESULTS: High‐performance liquid chromatography (HPLC) of pyrazosulfuron ethyl gave a single sharp peak at 3.41 min. The instrument detection limit (IDL) for pyrazosulfuron ethyl by HPLC was 0.1 µg mL?1, with a sensitivity of 2 ng. The estimated method detection limit (EMDL) was 0.001 µg mL?1 and 0.002 µg g?1 for water and soil respectively. Two applications at an interval of 10 days gave good weed control. The herbicide residues dissipated faster in water than in soil. In the present study, with a field‐soil pH of 8.2 and an organic matter content of 0.5%, the pyrazosulfuron ethyl residues dissipated with a half‐life of 5.4 and 0.9 days in soil and water respectively. Dissipation followed first‐order kinetics. Under laboratory conditions, degradation of pyrazosulfuron ethyl was faster in non‐sterile soil (t1/2 = 9.7 days) than in sterile soil (t1/2 = 16.9 days). CONCLUSION: Pyrazosulfuron ethyl is a short‐lived molecule, and it dissipated rapidly in field soil and water. The faster degradation of pyrazosulfuron in non‐sterile soil than in sterile soil indicated microbial degradation of this herbicide. Copyright © 2012 Society of Chemical Industry  相似文献   

15.
The effects of the fungicides benomyl, thiophanate-methyl and triadimefon on the chrysomelid beetle Gastrophysa polygoni were investigated in the laboratory. Contact with a suspension of benomyl (1.5 g a. i. litre?1 did not affect the hatchability of the eggs. Larvae were reared on shoots of knotgrass (Polygonum aviculare) that had been sprayed with suspensions of benomyl, ranging in concentration from 0.1 to 5.0 g a. i. litre?1. The mortality to the adult stage, of larvae reared on shoots treated with concentrations of benomyl of 0.5 g a. i. litre?1 and above, was significantly higher than that of control larvae. At concentrations of 2.0 g a. i. litre?1 and above, no larvae survived to the adult stage. The LD50 was 0.78 g a. i. benomyl litre?1. The LT50 values at concentrations of 1.0, 2.0 and 5.0 g a. i. benomyl litre?1 were 22.6, 12.6 and 5.3 days, respectively. The mean weights of adults bred from larvae that had been reared on shoots treated with benomyl (0.5 and 1.0 g a. i. litre?1) were significantly less than those of adults bred from control larvae. The mortality of larvae, reared on shoots of P. aviculare treated with triadimefon (0.5 g a. i. litre?1) or thiophanate-methyl (1.0 g a. i. litre?1), was also significantly higher than that of control larvae. Females kept on plants of P. aviculare treated with benomyl (1.5 g a. i. litre?1) laid similar numbers of eggs to those kept on untreated plants, and the hatchability of the eggs was not affected.  相似文献   

16.
The effects of a range of herbicide doses on crop–multiple weed competition were investigated. Competitivity of Galium aparine was approximately six times greater than that of Matricaria perforata with no herbicide treatment. Competitivities of both weeds decreased with increasing herbicide dose, being well described by the standard dose–response curve with the competitivity of M. perforata being more sensitive than that of G. aparine to a herbicide mixture, metsulfuron‐methyl and fluroxypyr. A combined model was then developed by incorporating the standard dose–response curve into the multivariate rectangular hyperbola competition model to describe the effects of multiple infestation of G. aparine and M. perforata and the herbicide mixture on crop yield. The model developed in this study was used to predict crop yield and to estimate the herbicide dose required to restrict crop yield loss caused by weeds to an acceptable level. At the acceptable yield loss of 5% and the weed combination of 120 M. perforata plants m?2 and 20 G. aparine plants m?2, the model recommends a mixture of 1.2 g a.i. ha?1 of metsulfuron‐methyl and 120 g a.i. ha?1 of fluroxypyr.  相似文献   

17.
研究了稻田施用氯氟吡氧乙酸后,其在水稻植株、糙米、稻壳、稻田土壤和田水中的残留动态。样品采用氢氧化钠-甲醇溶液振荡提取,二氯甲烷液液分配,甲酯化后经气相色谱-电子捕获检测器(GC-ECD)测定。结果表明:氯氟吡氧乙酸在水稻植株、稻田土壤、田水、糙米和稻壳中的平均 回收率在85.5% ~103.2%之间,相对标准偏差在1.9% ~9.9%之间;其最小检出量为2.0×10-12g, 在植株、糙米、稻壳、土壤和田水中的最低检测浓度分别为 0.005,0.02,0.005,0.002 mg/kg 和0.001 mg/L。2007和2008年在安徽潜山、广东广州两地的田间残留试验结果表明:氯氟吡氧乙酸在水稻植株中的降解半衰期为4.9 ~6.0 d,土壤中为5.5 ~8.6 d,田水中为11.0~13.8 d;收获的糙米中氯氟吡氧乙酸的最终残留量在未检出~0.13 mg/kg之间,均低于其在糙米上的最大残留限量(MRL)值0.2 mg/kg(中国)。建议5%氯氟吡氧乙酸可湿性粉剂用于防治水稻田杂草时,施药剂量按有效成分计不得超过168.8 g/hm2,于返青期施药1次。  相似文献   

18.
Freundlich isotherms were obtained for the adsorption equilibrium of the herbicides metamitron and chloridazon with the components of a representative soil in a pesticide concentration range of 10-1000 γg ml?1 for metamitron and 10-500 μg ml?1 for chloridazon. The mobility of these herbicides through soil columns was also studied using the displacement technique described by Davidson (Soil Sci. Soc. Amer. Proc., 32 (1968) 629). The experiment was carried out simultaneously in three columns, two of which were fed with solutions of the herbicides while the third was used as a control. The herbicide solutions flowed down by gravity and were collected at the outlet at different times. The herbicide content of these outlet solutions was determined by Differential Pulse Polarography.  相似文献   

19.
The depletion of zeta‐cypermethrin residues in bovine tissues and milk was studied. Beef cattle were treated three times at 3‐week intervals with 1 ml 10 kg?1 body weight of a 25 g litre?1 or 50 g litre?1 pour‐on formulation (2.5 and 5.0 mg zeta‐cypermethrin kg?1 body weight) or 100 mg kg?1 spray to simulate a likely worst‐case treatment regime. Friesian and Jersey dairy cows were treated once with 2.5 mg zeta‐cypermethrin kg?1 in a pour‐on formulation. Muscle, liver and kidney residue concentrations were generally less than the limit of detection (LOD = 0.01 mg kg?1). Residues in renal‐fat and back‐fat samples from animals treated with 2.5 mg kg?1 all exceeded the limit of quantitation (LOQ = 0.05 mg kg?1), peaking at 10 days after treatment. Only two of five kidney fat samples were above the LOQ after 34 days, but none of the back‐fat samples exceeded the LOQ at 28 days after treatment. Following spray treatments, fat residues were detectable in some animals but were below the LOQ at all sampling intervals. Zeta‐cypermethrin was quantifiable (LOQ = 0.01 mg kg?1) in only one whole‐milk sample from the Friesian cows (0.015 mg kg?1, 2 days after treatment). In whole milk from Jersey cows, the mean concentration of zeta‐cypermethrin peaked 1 day after treatment, at 0.015 mg kg?1, and the highest individual sample concentration was 0.025 mg kg?1 at 3 days after treatment. Residues in milk were not quantifiable beginning 4 days after treatment. The mean concentrations of zeta‐cypermethrin in milk fat from Friesian and Jersey cows peaked two days after treatment at 0.197 mg kg?1 and 0.377 mg kg?1, respectively, and the highest individual sample concentrations were 2 days after treatment at 0.47 mg kg?1 and 0.98 mg kg?1, respectively. © 2001 Society of Chemical Industry  相似文献   

20.
A competitive enzyme‐linked immunosorbent assay (ELISA) has been developed for the detection of the insecticide flucythrinate in environmental and food samples. Two types of haptens, the acid moiety that is the hydrolyzed product of flucythrinate, and the carboxylated propyl derivative of the alcohol moiety, were used to prepare monoclonal antibodies (MAbs). Five MAbs, which raised against the former hapten, were reactive with flucythrinate. Among them, MAb F1A27‐4 showed the highest activity toward flucythrinate, and did not cross‐react with other pyrethroids such as cycloprothrin, fenvalerate, fluvalinate, etofenprox and silafluofen. The assay conditions of indirect competitive ELISA with MAb F1A27‐4 were studied to optimize the detection of flucythrinate in environmental and food samples. Incubation at 4 °C in the assay buffer, pH 8, with 300 mM sodium chloride improved the sensitivity. The addition of rabbit serum albumin or rabbit antiserum and the presence of 50 ml litre?1 of methanol reduced matrix effects of the samples. Under optimized conditions, the ELISA detected flucythrinate spiked in water, soil, and extracts of apple and tea samples down to 10 mg litre?1, 0.2 mg litre?1, 0.3 mg litre?1 and 0.3 mg litre?1, respectively. The mean recovery and CV ranged from 91% to 120% and from 5% to 12%, respectively. The ELISA results in apple samples correlated well with those from LC–MS analysis (r2 = 0.99, n = 12). © 2001 Society of Chemical Industry  相似文献   

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