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1.
Nine fungicides that inhibit ergosterol biosynthesis (diclobutrazol, fenarimol, fenpropimorph, imazalil, nuarimol, prochloraz, propiconazole, triadimefon, triadimenol) and one plant growth regulator (ancymidol) were administered to Japanese quails (Coturnix coturnix). Most of these compounds had a moderate or no effect, but prochloraz, imazalil and, to a lesser extent, propiconazole were shown to produce a dramatic increase in liver weight and cytochrome P-450 level. These three compounds were also found to be potent in-vitro inhibitors of 7-ethoxycoumarin O-de-ethylase and aniline hydroxylase, thus resulting in a biphasic effect on drug-metabolising enzymes. With these three compounds, and some others, an accumulation of lanosterol in liver was also observed, suggesting an inhibition of sterol synthesis.  相似文献   

2.
Prochloraz (N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]-imidazole-1-carboxamide), a recently developed agricultural fungicide, is a potent inducer of microsomal enzymes. Rats fed 7 days with a prochloraz-contaminated diet (2500 ppm) showed an increase in hepatic cytochrome P-450, cytochrome b5, and microsomal protein level; aniline hydroxylase, 7-ethoxycoumarin dealkylase, 7-ethoxyresorufin dealkylase, NADPH-cytochrome c reductase, and epoxide hydrolase were significantly induced. At a lower dose (100 ppm), only an increase in cytochrome P-450 and 7-ethoxyresorufin dealkylase was noticed. As shown with aniline hydroxylase and 7-ethoxycoumarin dealkylase, prochloraz is also a potent inhibitor of drug-metabolizing enzymes. The interaction of prochloraz with hepatic microsomal fraction from rat liver was also studied. Prochloraz binds to oxidized cytochrome P-450 to produce a type II spectral change; the compound also binds to reduced cytochrome P-450. The binding of some ligands (7-ethoxycoumarin, n-octylamine, aniline, and imidazole) to oxidized cytochrome P-450 was determined after induction by prochloraz. Japanese quails (Coturnix coturnix) fed 7 days with a prochloraz-contaminated diet (2000 ppm) showed a dramatic increase in liver weight (2.5-fold) and both hepatic and duodenal cytochrome P-450 (9- and 12-fold, respectively).  相似文献   

3.
In a dietary toxicity study, laying hens received a diet containing the rodenticide flocoumafen at concentrations of 1.5, 5, 10 and 50 mg kg?1 for five consecutive days. The LC50 at termination following a 28-day observation period was 16.4 mg kg?1. Livers of birds which received doses of flocoumafen between 5 and 50 mg kg?1 had concentrations of flocoumafen (1.5 nmol g?1) that were independent of dose. The data indicate the presence in hen liver of a saturable high-affinity flocoumafen binding site with similar characteristics and capacity to that of the quail and rat. Residues of flocoumafen in samples of breast and leg muscle were low in all exposure groups. Higher, dose-related residues were found in samples of abdominal fat and skin-associated fat and there was a clear demonstration of the transfer of dose-related residues into eggs. In a separate study in which hens were dosed with [14C]flocoumafen for five consecutive days at a daily rate of 1 and 4 mg kg?1 body weight, the majority (68 %) of the daily radioactive dose was eliminated over the following 24 hours via excreta. Residues in liver at death or when killed accounted for < 1 % of the cumulative administered radioactivity. Residues in eggs were located primarily in the yolk with maximum concentrations 1.0 mg kg?1 or 0.18% of the low dose; 2.1 mg kg?1 or 0.06% of the high dose as [14C]flocoumafen equivalents were observed at 10 days after start of dosing. Some 40 % of the total activity in the yolk was unchanged flocoumafen.  相似文献   

4.
Methods are described for the extraction and analysis by gas-liquid and high-pressure liquid chromatography of the fungicide imazalil, 1-(β-allyloxy-2, 4-dishlorophenethyl) imidazole, on potatoes. Before storage, over 80% was recovered from potatoes treated with 0.01–3.0 mg imazalil kg?1, with a detection limit of 2 μg kg?1. Imazalil applied to potatoes at 10 g t?1 before storage decreased the incidence of gangrene (Phoma exigua), silver scurf (Helminthosporium solani), skin spot (Polyscytalum pustulans) and black scurf (Rhizoctonia solani), and was at least as effective as thiabendazole applied at 40 g t?1. At 1 g t?1 it also decreased skin spot and silver scurf. Incidence of black dot (Colletotrichum coccodes) was unaffected by these fungicide treatments.  相似文献   

5.
The chitin synthesis inhibitor diflubenzuron, applied as a wettable powder spray to woven polypropylene at 100–500 mg m?2, was effective against Dermestes maculatus De Geer for at least 12 weeks. D. maculatus was unable to develop on ox hide dipped in a suspension of diflubenzuron (125 mg litre?1), or on fishmeal dusted at 1–10 mg of active ingredient kg?1. Diflubenzuron prevented the development of infestations of Callosobruchus maculatus (L.) on peas and of Acanthoscelides obtectus (Say) on beans dusted at 1–5 mg kg?1. The compound was also very effective against early instar larvae of Trogoderma granarium Everts on wheat. The persistence and activity of diflubenzuron at low dosage rates against D. maculatus appear to justify larger scale trials.  相似文献   

6.
Development and phenobarbital (PB) induction of microsomal cytochrome P-450, cytochrome P-450 reductase, two epoxidation, and two O-demethylation activities were examined in chronologically timed populations of insecticide-susceptible (NAIDM) and -resistant (Rutgers) house flies. Measurements of these enzymes started with the pharate adult stage and ended 5 days following eclosion. Untreated insects of both strains had comparable reductase levels, whereas cytochrome P-450 and associated monooxygenase activities were 1.5-fold or more higher in Rutgers. Maximum induction, as well as toxicity, occurred at a lower PB concentration in NAIDM than Rutgers. The drug caused consistently higher increases in enzymes and activities within 12 hr of starting treatment in both strains. When PB was withdrawn from treated flies (both strains) 48 hr after treatment began, specific activities (product min?1 mg protein?1) in all enzymes returned to control values in 24 hr while metabolic capacity (product min?1 insect?1) achieved control values within 48 hr. The changes in turnover numbers (pmol product min?1 pmol P-450?1), in conjunction with the differences in the monooxygenation of the four substrates, suggest that PB treatment induced both a quantitative and qualitative change in NAIDM monooxygenation but only a quantitative change in Rutgers monooxygenation.  相似文献   

7.
In the Japanese quail, cytochrome P-450, A- and B-esterase, amidase, and glutathione S-aryl transferase were assayed in postmitochondrial centrifugal fractions, in microsomes, and supernatant fractions of liver, lungs, kidneys, and testes. Liver microsomes contained the highest A-esterase activity and P-450 levels. B-esterase was more generally distributed and higher in the microsomal tissue fractions. Microsomal amidase activity was highest in quail lung and kidney, and lowest in the liver (per mg protein). Very little difference in glutathione S-aryl transferase activity was noted among the tissues assayed. In vitro metabolism of carbaryl, phosphamidon, and chlorotoluron by the various centrifugal fractions revealed that the production of 1-naphthyl-N-hydroxymethylcarbamate and 1-naphthol, the major metabolites, was greatest in the postmitochondrial fraction of the liver. The major carbaryl metabolite in all other quail tissue fractions was 1-naphthol. Phosphamidon metabolism in postmitochondrial preparations of quail liver was higher than in the supernatant and microsomes. Chlorotoluron metabolism occurred only in the postmitochondrial fractions of quail liver. The major products were the oxidative metabolites, N-(3-chloro-4-methylphenyl)-N′-methylurea and N-(3-chloro-4-hydroxymethylphenyl)-N′-methylurea.  相似文献   

8.
BACKGROUND: A mixture of trifloxystrobin and tebuconazole is excellent in controlling both powdery and downy mildew of grapes. The objective of the present work was to study the behaviour of trifloxystrobin and tebuconazole on grape berries and soil following treatment with Nativo 75 WG, a formulation containing both fungicides (trifloxystrobin 250 + tebuconazole 500 g kg?1). This study was carried out for planned registration of this mixture for use on grapes in India. RESULTS: Initial residue deposits of trifloxystrobin and tebuconazole on grapes were below their maximum residue limit (MRL) of 0.5 and 2 mg kg?1, respectively, when Nativo 75 WG was applied at the recommended dose of 175 g product ha?1. The residues dissipated gradually to 0.02 and 0.05 mg kg?1 by 30 days, and were below the quantifiable limit of 0.01 mg kg?1 at the time of harvest (60 days after the last treatment). Trifloxystrobin and tebuconazole dissipated at a pre‐harvest interval (PHI) of 36 and 34 days, respectively, from the recommended treatment dose. The acid metabolite of trifloxystrobin, CGA 321 113, was not detected in grape berries at any point in time. Soil at harvest was free of any pesticide residues. CONCLUSION: Residue levels of both trifloxystrobin and tebuconazole were below MRLs when grapes were harvested 30 days after the last of four applications of 175 g product ha?1 (trifloxystrobin 44 g AI ha?1, tebuconazole 88 g AI ha?1) under the semi‐arid tropical climatic conditions of India. Copyright © 2010 Society of Chemical Industry  相似文献   

9.
A goat was dosed orally with [14C]tefluthrin, twice daily for 4 days, at a rate equivalent to 10.9 mg kg?1 in its diet. Within 16 h of the final dose, 70.1% of the dose had been excreted (urine 41.4%, faeces 28.7%). Extensive metabolism occurred in the goat by ester cleavage and oxidation at a variety of positions on the molecule. Low radioactive residues were detected in the milk (0.076 mg kg?1), fat (0.076 mg kg?1) and muscle (0.016 mg kg?1), with tefluthrin as the largest individual component of the residue (milk 66.5%, fat 76.7%, muscle 34.2%). Higher residues were present in the kidney (0.3 mg kg?1) and liver (1.0 mg kg?1) and only a small percentage of this residue was due to tefluthrin (kidney 3.4%, liver 6.1%). The remainder of the residue in the kidney and liver was a complex mixture of metabolites. Most of the kidney metabolites were identified, but a high proportion of the liver residue was due to six unidentified polar compounds.  相似文献   

10.
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   

11.
Permethrin and deltamethrin, two synthetic pyrethroid insecticides, are registered in several countries for use on lettuce. Both chemicals were applied on autumn and spring grown lettuce in the glasshouse. When applied at the normal prescribed dose rates of 25 and 12.5 g a.i. ha?1, < 1 mg kg?1 of either compound was found in the lettuce at harvest, even when applied only a few days before harvest. The total amount of active ingredient applied was too low to reach the 1 mg kg?1 level when evenly applied on marketable lettuce heads weighing about 200 g each. Applying a higher dose than 25 g permethrin a.i. ha?1 or 12.5 g deltamethrin a.i. ha?1, or applying two applications in the 2 weeks prior to harvest, may well result in residue levels higher than the maximum residue limit of 1 mg kg?1 for permethrin and certainly higher than the maximum residue limit of 0.2 mg kg?1 for deltamethrin, which is more persistent.  相似文献   

12.
Sorghum (Sorghum bicolor (L.) Moench) plants were grown in pots with 12.5 and 50 mg applied N kg?1 soil. With an increase of soil N, the Striga asiatica (L.) Kuntze infestation, as well as the sorghum shoot dry matter losses due to infestation, decreased. The relative differences in stimulant capacity to induce Striga seed germination among the four sorghum genotypes were not consistent over the 0 to 150 mg N 1?1 range. The sorghum root exudate was considerably more active at 0 mg N 1?1, than at 30 mg N 1?1, and the stimulant produced at 150 mg N 1?1 failed to induce Striga seed germination. Presence of N in the growth medium considerably reduced the effectiveness of the stimulating substance produced by sorghum roots, whereas K promoted stimulant activity only in the absence of N. The presence or absence of P in the growth medium did not affect Striga seed germinability, probably due to the inability of this element to interfere with the production or activity of the stimulating substance from the host plants. It can be concluded, therefore, that sorghum plants seem to produce active root exudate only in conditions of N deficiency.  相似文献   

13.
Following experimental and commercial applications to soil of a granular formulalation of phorate (O,O-diethyl S-ethylthiomethyl phosphorodithioate), residues in the soil and in lettuce were determined by gas-liquid chromatography. When applied by the bow-wave method as a continuous logarithmically-changing dose ranging from approximately 0.9 to 16.0 kg a.i. ha?1, the proportional rate of oxidation in soil of phorate sulphoxide to phorate sulphone was inversely related to dose. Ten weeks after application, total phorate residues in the soil had declined by about 35% at all dose levels. Residues in mature lettuce, from the 1-5 kg ha?1 dose-range, comprised the parent and oxygen analogue sulphoxides and sulphones; the relative proportions of the individual metabolites were independent of dose. Over this dose-range, total residue concentrations in the crop became proportionally slightly greater with increasing dose. When single doses of 1.1, 2.0 or 2.2 kg a.i. ha?1 were applied at drilling, the total residue concentrations in the lettuce declined from 5 mg kg?1 in seedlings from some treatments to <0.05 mg kg?1 at harvest. In plants raised in peat blocks containing 10 or 20 mg a.i. per block, however, residues in seedlings totalled 45-47 mg kg?1 and declined to only 0.7 mg kg?1 at harvest. It was concluded that bowwave applications of phorate when field-sowing lettuce were unlikely to lead to unacceptable residues in the harvested crop, but that residues in lettuce raised in phorate-treated peat blocks may be unacceptably high.  相似文献   

14.
Rape seedlings grown from seeds treated with a gamma-HCH seed dressing at a dose rate of 15.7 g kg?1 had a maximum gamma-HCH concentration of 380 mg kg?1 in seedlings collected 1 day after emergence. The mean gamma-HCH concentration in the seedlings decreased to 2.6 and to 0.9 mg kg?1 by 7 and 15 days after emergence, respectively. Gamma-HCH was chemically detected in true leaves, at concentrations up to 1.9 mg kg?1, indicating translocation of gamma-HCH in young plants.  相似文献   

15.
Field trials with various pesticide combinations were carried out on bulk wheat in commercial silos in Queensland, South Australia and Western Australia. Laboratory bioassays on samples of treated grain at intervals over 8 months using malathion-susceptible and malathion-resistant strains established the following orders of efficacy: against Sitophilus oryzae (L.), chlorpyrifos-methyl 10 mg kg?1 + bioresmethrin 1 mg kg?1 = methacrifos 15 mg kg?1 in aerated storage > pirimiphos-methyl 4 or 6 mg kg?1 + bioresmethrin 1 mg kg?1 = bioresmethrin 4 mg kg?1 + piperonyl butoxide 16 mg kg?1; against Rhyzopertha dominica (F.), bioresmethrin 4 mg kg?1 + piperonyl butoxide 16 mg kg?1 > methacrifos 15 mg kg?1 > chlorpyrifos-methyl 10 mg kg?1 + bioresmethrin 1 mg kg?1 = pirimiphos-methyl 4 or 6 mg kg?1 + bioresmethrin 1 mg kg?1. All treatments completely prevented production of progeny in Sitophilus granarius (L.), Tribolium castaneum (Herbst), T. confusum Jackquelin du Val and Oryzaephilus surinamensis (L.). The biological efficacy of methacrifos was greater and the rate of degradation lower in aerated than in non-aerated storage. Residue levels of all compounds were determined chemically and were below proposed international residue levels to be considered by the Codex Alimentarius Commission.  相似文献   

16.
Eight amino-substituted derivatives of 1-amino-benzotriazole (ABT) were synthesized and tested. N-acetyl-N-methyl ABT (AcMeABT) was found to kill maize (Zea mays L.) hybrid Pioneer 3737 at 5 kg ha?1 dose while ryegrass (Lolium perenne L.) was unaffected. The analogous N-propionyl-N-methyl ABT had an activity similar to AcMeABT whereas other N-acyl-N-alkyl derivatives had only moderate or no effects on maize. AcMeABT was considerably toxic to oats (Avena sativa L.) and sorghum (Sorghum bicolor L.) as well. Unlike ABT, AcMeABT did not show any in vitro inhibitory effect on cytochrome P-450 enzymes of maize microsomes. However, in vivo AcMeABT pre-treatment significantly decreased the microsomal cytochrome P-450 level of aetiolated maize seedlings. Moreover, a subtoxic dose of AcMeABT was a weak antagonist of a toxic dose of EPTC in maize in vivo. These data predict the involvement of cytochrome P-450 enzyme in the mode of action of AcMeABT. N-acyl-N-alkyl l-aminobenzotriazoles: phyto-toxicité, antagonisme avec l'EPTC et effets sur le cytochrome P-450 du maïe Huit dérivés sur le groupement amine de l'1-aminobenzotriazole (ABT) ont été synthétisés. Une dose 5 kg ha?1 de N-acétyl-N-méthyl ABT (AcMeABT) détruisait le maïs (Zea mays L.) hy-bride Pioneer 3737 alors que le raygrass (Lolium perenne L.) n'était pas affecté. L'analogue N-propionyl-N-méthyl ABT avail une activité simi-laire à celle de l' AcMeABT, alors que les autres dérivés N-acyl-N-aklyl n'avaient que des effets nuls ou faibles surle maïs. L'AcMeABTétait très toxique à l'égard de l'avoine (Avena sativa L.) et du sorgho bicolore (Sorghum bicolor L.). Con-trairement à l'ABT, l'AcMeABT n'inhibait pas in vitro les enzymes P-450 des microsomes du maïs. Cependant, un pré-traitement in vivo a l'AcMeABT diminuait significativement le niveau de cytochromes P-450 microsomaux de jeunes plantes étiolées de maïs. En outre, une dose subtoxique d'AcMeABT avail sur maïs in vivo un effet antagoniste faible contre une dose loxique d'EPTC. Ces données suggèrent l'impli-cation d'enzymes cytochrome P-450 dans le mode d'action de l'AcMeABT. Phytotoxizität, Antagonismus gegenüber EPTC und Wirkungen auf das Cytochrom P-450 von N-Acyl-N-alkyl-1-aminobenztriazolen Bei Versuchen mit 8 Amino-subslituierten Deri-vaten von 1-Aminobenzotriazol (ABT) war N-Acetyl-N-methyl-1-aminobenztriazol (AcMeABT) mit 5 kg ha?1 für Mais (Zea mays L.) ‘Pionier 3737’ phyloloxisch, für Deulsches Weidelgras (Lolium perenne L.) nicht. Das analoge N-Propionyl-N-methyl-1-aminobenztriazol war ähnlich wirksam wie AcBeABT, andere Deri-vale kaum oder gar nichte. AcMeABT war für Saat-Hafer (Avena sativa L.) und Sorghumhirse (Sorghum bicolor L.) erheblich phytotoxisch. Anders als ABT zeigte AcMeABT in vitro keine Hemmwirkung auf das Cytochrom P-450 in Mais-Mikrosomen, in vivo jedoch nahm der Cy-tochrom-P-450-Gehalt etiolierter Mais-keimpflanzen nach AcMeABT-Behandlungen signifikantab. Außerdem war eine subtoxische Dosis von AcMeABT schwach antagonistisch für eine für Mais toxische EPTC-Dosis. Diese Daten weisen auf die Beteiligung des Cytochrom-P-450-Enzyms an der Wirkungsweise des AcMeABT hin.  相似文献   

17.
Phorate residues in peat blocks and lettuce were determined following incorporation of the insecticide into different block and ‘Speedling’ cell sizes. Between-block variability was influenced little by block size. Phorate oxidation was most extensive in the largest blocks containing the smallest dose. Total residue concentrations in the lettuce declined from the time of planting to harvest, although accumulation of insecticide continued and was related more to dose than to block or cell size. Residues in the lettuce at harvest exceeded the proposed maximum limit of 0.2 mg kg?1 in some treatments. Residues at planting comprised mainly the parent sulphoxide and sulphone, but by harvest, the oxygen analogue sulphoxide and sulphone predominated. Lettuce weight was not influenced by dose but was related directly to block size. Carbofuran and chlorfenvinphos residues were determined in calabrese sown into two sizes of blocks. At planting time, carbofuran residue concentrations were 100 times greater than those of chlorfenvinphos but residues of both insecticides in the mature heads were < 0.01 mg kg?1. Seedling weights in both sowings declined with increasing concentrations of the insecticides. It was concluded that manipulations of block size and the dose of insecticide need to be evaluated for individual insecticide/crop combinations to exploit the technique fully.  相似文献   

18.
In laboratory experiments, whole wheat was treated with pirimiphos-methyl or carbaryl or combinations of these two insecticides; the treated grain was then adjusted to a 12% moisture content and stored at 25°C for bioassay at various intervals over a period of 39 weeks. Pirimiphos-methyl at 5.1 mg kg?1 effectively controlled Sitophilus granarius (L.) and Tribolium confusum Jacquelin du Val but was ineffective against Rhyzopertha dominica (F.) CRD 118, a strain showing malathion resistance. Conversely, carbaryl at 6.5 mg kg?1 (but not at 3.1 mg kg?1) was effective against R. dominica, but ineffective against the other two species. A combination of pirimiphosmethyl + carbaryl, at 1.8 + 5.1 mg kg?1, controlled S. granarius and R dominica but not T. confusum, whilst a 4.2 + 3.4 mg kg?1 combination was relatively more effective against T. confusum but less so against R. dominica. In a separate experiment, whole wheat was treated with carbaryl at 2.5, 5.0 and 7.5 mg kg?1 (nominal rates). Samples were stored and, at various times after the treatments, were bioassayed with R. dominica CRD 2, at 20, 25, 30 and 35°C. The results were comparable with those for the CRD 118 strain, but efficacy was reduced at higher temperatures. The combination of pirimiphos-methyl at 4–5 mg kg?1 and carbaryl at 5–6 mg kg?1 is suggested as a potentially useful grain protectant where R. dominica is a problem and long term storage is required. These results are discussed in relation to the protection of stored grain in Australia.  相似文献   

19.
Organophosphorothioates and synergised synthetic pyrethroids were used in duplicate field trials carried out on bulk wheat in commercial silos in Queensland and New South Wales. Laboratory bioassays using malathion-resistant strains of insects were carried out on samples of treated grain at intervals over 9 months. These established that all treatments were generally effective. Deltamethrin (2 mg kg?1)+ piperonyl butoxide (8 mg kg?1), fenitrothion (12 mg kg?1)+ fenvalerate (1 mg kg?1)+ piperonyl butoxide (8 mg kg?1), fenitrothion (12 mg kg?1)+ phenothrin (2 mg kg?1)+ piperonyl butoxide (8 mg kg?1) and pirimiphos-methyl (4 mg kg?1)+ permethrin (1 mg kg?1)+ piperonyl butoxide (8 mg kg?1) controlled common field strains of Sitophilus oryzae (L.) and Rhyzopertha dominica (F.). Against a highly resistant strain of S. oryzae, deltamethrin (2 mg kg?1)+ piperonyl butoxide (8 mg kg?1) was superior to the remaining treatments. All treatment combinations completely prevented progeny production in Tribolium castaneum (Herbst), T. confusum Jacquelin du Val and in Ephestia cautella (Walker). Residues of deltamethrin, fenvalerate, permethrin and phenothrin were determined and shown to be highly persistent on stored wheat. During milling, residues accumulated in the bran fractions and were reduced in white flour. They were not significantly reduced during baking.  相似文献   

20.
Residues of the herbicide dinoseb were determined gas chromatographically in lentils which had been treated at two locations in Saskatchewan with post-emergence applications of dinoseb at 1.4 and 1.7 kg ha?1. Herbicide residues, determined at selected times after application, were not detected at the limit of detection of the analytical method (0.05 mg kg?1) in either the seed and straw at maturity, or in the green foliage six to eight weeks after application. Recoveries of dinoseb were 76% from fortified green foliage at the 0.1 mg kg?1 level, and 64% from fortified seed at the 0.05 mg kg?1 level.  相似文献   

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