Examination of stability of resistance and cross-resistance patterns to acylurea insect growth regulators in field populations of the diamondback moth,Plutella xylostella,from Malaysia

In teflubenzuron and teflubenzuron/chlorfluazuron laboratory-selected sub-populations of a Cameron Highlands (1988) strain of Plutella xylostella L., resistance to teflubenzuron reached much greater levels than chlorfluazuron but declined at a correspondingly greater rate to give similar resistance levels after 10–13 generations. There was little evidence of cross-resistance to flufenoxuron and none to hexaflumuron in these populations. Reselection of a Cameron Highlands population with teflubenzuron after 22 generations resulted in a significant (P < 0.05) increase in resistance after three generations. In two more recently collected strains from lowland Malaysia, Sawi (1991) and Serdang (1992) high levels of resistance to teflubenzuron were found, but only the former showed any apparent resistance to chlorfluazuron. There was also evidence of resistance to diflubenzuron in the Sawi strain (Serdang not examined). Resistance to teflubenzuron appeared to be unstable in unselected sub-populations of both lowland strains. Selection of the Sawi strain with teflubenzuron did not effect cross-resistance to chlorfluazuron, while attempted selection with chlorfluazuron had no effect on resistance to either compound. Selection of the Sawi strain with diflubenzuron increased resistance to teflubenzuron but had no effect on resistance to chlorfluazuron. In contrast to the Sawi strain, selection of the Serdang strain with teflubenzuron resulted in cross-resistance to chlorfluazuron. Synergist experiments with piperonyl butoxide (PB) and S,S,S-tributyl phosphorotrithioate (DEF) suggested that resistance to teflubenzuron in the lowland strains may involve both microsomal monooxygenases and esterases. The ovicidal activity of teflubenzuron, chlorfluazuron, hexaflumuron and flufenoxuron was consistently less than their activity against second-instar larvae, hexaflumuron, followed by teflubenzuron, showing the greatest relative ovicidal activity. Hexaflumuron was markedly more active than teflubenzuron against eggs from acylurea-selected Cameron Highlands populations and there was some evidence that resistance to teflubenzuron may be expressed at a lower level in eggs than in larvae in one such strain.     

The inhibition of chitin synthesis in spodoptera littoralis larvae by flufenoxuron,teflubenzuron and diflubenzuron

The chitin precursor [¹⁴C] N-acetylglucosamine injected into the haemolymph of Spodoptera littoralis (Boisduval) larva was incorporated into the chitin exponentially with time. When caterpillars were injected with precursor at the commencement of feeding on acylurea-treated leaf discs, flufenoxuron, teflubenzuron and diflubenzuron were found to be equally effective inhibitors of chitin synthesis, measured after 21 h. The dose response curves by feeding are not parallel, indicating that the relative potency of the compounds will vary across the dose range. When chitin precursor was injected simultaneously with topically applied diflubenzuron, flufenoxuron or teflubenzuron, all three acylureas were found to be equally effective as inhibitors of chitin synthesis when measured after five hours. The I₅₀values (50% inhibition of chitin synthesis) were not significantly different; average 600 ng, compared with LD₅₀values (50% lethal dose) of ～ 13 ng for flufenoxuron and teflubenzuron but 130 ng for diflubenzuron (topical application). Injection of precursor 24 h after topical application of insecticide gave an I₅₀value which had dropped 670- and 150-fold for flufenoxuron and teflubenzuron respectively but only 20-fold for diflubenzuron. It is postulated that the reason for the low increase in diflubenzuron effectiveness with time was due either to less diflubenzuron than flufenoxuron reaching the site of action, or more probably, a faster rate of metabolism and excretion for diflubenzuron. The lower toxicity of diflubenzuron compared with flufenoxuron and teflubenzuron may not be due to any inherent differences in biochemical effectiveness, but rather to different penetration/metabolism properties.     

Persistence of insect growth regulators against the rice weevil,sitophilus oryzae,in grain commodities

Ten insect growth regulators (IGRs): four juvenile hormone analogs (JHAs) — fenoxycarb, MV-678, R-20458 and dofenapyn, and six molt inhibitors (MIs) — triflumuron, chlorfluazuron, hexaflumuron, teflubenzuron, Dowco 439 and flufenoxuron; and the organophosphate malathion, were evaluated for residual activity in stored grain for 2 years against the rice weevil,Sitophilus oryzae (L.). Triflumuron, flufenoxuron, teflubenzuron, chlorfluazuron, hexaflumuron and fenoxycarb, each at a concentration as low as 1 ppm a.i., were superior to 10 ppm malathion throughout the experiment. The six MIs, each tested at 50 and 100 ppm a.i., gave complete control for 2 years. Moreover, a concentration as low as 1 ppm a.i. of triflumuron, teflubenzuron, flufenoxuron and chlorfluazuron had good residual activity for 1 year post-treatment and provided almost complete grain protection during this period. Among the JHAs, fenoxycarb had the best residual activity. It gave almost complete control (96.6%) ofS. oryzae at 10 ppm for 18 months post-treatment. The other JHAs at the four test concentrations failed to produce this level of control. The viability of the wheat grain was not affected by any of the insecticidal treatments, with 90% germination recorded in treated and control, grains at all intervals tested.     

Cross-resistance between acylurea insect growth regulators in a strain of Plutella xylostella L. (Lepidoptera: Yponomeutidae) from Malaysia

The activities of the acylurea insect growth regulators, chlorfluazuron, teflubenzuron and difubenzuron, and the neurotoxic macrocyclic lactone, abamectin were assessed against a laboratory susceptible (FS) strain and a field (Cameron Highlands, Malaysia (CH)) strain of the diamondback moth, Plutella xylostella L. using a leaf-dip bioassay at 20°C. The time taken to achieve end-point mortality was found to vary considerably (9–17 days), being fastest with abamectin against the FS strain and slowest with difubenzuron against the CH strain. The order of activity (LC₅₀ at F6/7) against second-instar larvae of both strains was: abamectin > chlorfluazuron = teflubenzuron ? difubenzuron. Subsequent assays (F14) with the acylureas, flufenoxuron and hexaflumuron against the FS strain suggested that the former was slightly more active than chlorfluazuron or teflubenzuron, the latter slightly less active. The CH population was found to be 12.6-, 6.7-, 6.4- and 2.3-fold less sensitive to difubenzuron, teflubenzuron, chlorfluazuron and abamectin respectively than the FS strain. Selection of sub-populations of the CH strain with chlorfluazuron (CHL-SEL) and teflubenzuron (TEF-SEL) for six generations (F6-11), resulted in LC₅₀ resistance ratios of 109- and 315-fold respectively when compared with the FS strain, equivalent to an 18- and a 46-fold increase in resistance compared with the unselected CH strain. Marked cross-resistance was also demonstrated between chlorfluazuron and teflubenzuron in both sub-populations. However, there was no evidence of cross-resistance to dijlubenzuron and abamectin and little or no cross-resistance to flufenoxuron and hexaflumuron. Resistance to chlorfluazuron and teflubenzuron appeared to be relatively unstable in the TEF-SEL compared with the CHL-SEL sub-population (over 6–9 generations). However, reselection of the TEF-SEL population with chlorfluazuron (F18–20) led to a very rapid increase in resistance to chlorfluazuron and particularly teflubenzuron. For the latter compound, resistance factors of about 1000000 were obtained (F19, 21). Such values are probably only semi-quantitative, as above a certain level of resistance feeding bioassays with acylureas (compounds which are active to a significant extent by ingestion) are likely to become rate-limiting.     

Comparative laboratory evaluation of the acute and chronic toxicology of diflubenzuron,hexaflumuron and teflubenzuron against II instar desert locust (Schistocerca gregaria) (Orthoptera: Acrididae)

The acute and chronic toxicities of three benzoylphenyl ureas, diflubenzuron, hexaflumuron and teflubenzuron were assessed under laboratory conditions against two-day-old second (II) instar Desert Locust, Schistocerca gregaria (ForskÅl) nymphs. Following exposure by ingestion of a single precise dose applied to short pieces of spring barley, nymphs were monitored for two moults until the fourth (IV) instar. Analysis of acute response data gave three significantly different LD₅₀ statistics (P < 0·05), 68·0, 26·6 and 0·71 μg per nymph respectively for diflubenzuron, hexaflumuron and teflubenzuron. The probit regression slopes also differed significantly, indicating distinct tolerance distributions for the three compounds, the narrowest response being to diflubenzuron and the widest range of response being to teflubenzuron. The timing of death was found to vary between the compounds; most nymphs died during the first moult following treatment with either hexaflumuron or teflubenzuron. However, the majority of nymphs that died after exposure to diflubenzuron did so after completing the first moult after treatment, but before the second. The mean development times of nymphs during the II and especially third (III) instars were significantly longer (P < 0·05) than those of the controls following exposure to diflubenzuron and hexaflumuron. Teflubenzuron had no significant effect (P < 0·05) on the duration of the II instar. The potential of the three compounds to control S. gregaria populations in the field is discussed with particular reference to the timing and nature of acute and chronic responses.     

Effect of insecticide—synergist combinations on the survival of Spodoptera exigua

The chitin synthesis inhibitors diflubenzuron and teflubenzuron have recently become ineffective for the control of Spodoptera exigua in floricultural crops. An extended laboratory test with second-instar larvae of S. exigua on Vicia faba plants was carried out to determine the influence of synergists on the biological activity of three benzoylphenyl ureas (BPUs). The co-application of piperonyl butoxide, an oxidase inhibitor, did not increase the activity of diflubenzuron, teflubenzuron or hexaflumuron. The best results were obtained with diethyl maleate, for suppressing glutathione S-transferase activity, and with dimethoate, as a hydrolase inhibitor. A joint application of diflubenzuron (at a concentration which resulted in 43% survival) with diethyl maleate or dimethoate gave only 6.2 and 8.9% surviving larvae, respectively. In addition, development to fourth-instar larvae was inhibited. The more stable teflubenzuron was synergized by both compounds to a much lesser extent than diflubenzuron. None of the synergists had a significant effect on the activity of hexaflumuron, which was the most potent insecticide of the three BPUs tested against S. exigua.     

Egg-sterilizing effect of benzoylphenylureasvia the adult stage of the nitidulid beetleCarpophilus hemipterus

The effect of a 24-h exposure of adults ofCarpophilus hemipterus to artificial diets treated on the surface with different concentrations of benzoylphenylureas, on the hatchability of eggs laid during the subsequent 14 days, was investigated. The order of persistence of sterilization at 5 ppm was chlorfluazuron (IKI-7899), 12 days > XRD-473, 10 days > diflubenzuron, 6 days > teflubenzuron (CME 134), 4 days. Three of the substances (chlorfluazuron, diflubenzuron and teflubenzuron) had no direct ovicidal effect whenC. hemipterus eggs were dipped in 1000 ppm dilutions, but the larvae that hatched from the treatments died within 2 days.     

Laboratory and field evaluation of spinosad against the gypsy moth,Lymantria dispar

The toxicity of the naturally derived insecticide spinosad was tested against the gypsy moth, Lymantria dispar. Bioassays using red oak leaf disks, treated with spinosad in a Potter spray tower, yielded an LC₅₀ value of 0.0015 µg AI cm⁻² (3‐day exposure; 13‐day evaluation; 2nd instar larvae). Applied to foliage to run‐off in the laboratory (potted red oak seedlings) and the field (4 m‐tall birch trees), spinosad effectively controlled 2nd instar larvae at concentrations ranging from 3 to 50 mg litre⁻¹. Toxicity in the laboratory, and efficacy and persistence in the field, were comparable to those achieved with the insecticide permethrin. Laboratory studies supported field observations that control was achieved in part by knockdown due to paralysis. In addition, laboratory results demonstrated that crawling contact activity may play an important role in field efficacy; 50% of treated larvae were paralyzed 16 h after a 2‐min crawling exposure to glass coated with a 4 mg litre⁻¹ spinosad solution. © 2000 Society of Chemical Industry     

Fumigant toxicity of volatile natural products from Korean spices and medicinal plants towards the rice weevil,Sitophilus oryzae (L)

The fumigant toxicity of various volatile constituents of essential oils extracted from sixteen Korean spices and medicinal plants towards the rice weevil, Sitophilus oryzae L (Coleoptera: Curculionidae), was determined. The most potent toxicity was found in the essential oil from Mentha arvensis L var piperascens (LC₅₀ = 45.5 µl litre^?1 air). GC–MS analysis of essential oil from M arvensis showed it to be rich in menthol (63.2%), menthone (13.1%) and limonene (1.5%), followed in abundance by β‐pinene (0.7%), α‐pinene (0.6%) and linalool (0.2%). Treatment of S oryzae with each of these terpenes showed menthone to be most active (LC₅₀ = 12.7 µl litre^?1 air) followed by linalool (LC₅₀ = 39.2 µl litre^?1 air) and α‐pinene (LC₅₀ = 54.9 µl litre^?1 air). Studies on inhibition of acetylcholinesterase activity of S oryzae showed menthone to have a nine‐fold lower inhibitory effect than menthol, despite menthone being 8.1‐fold more toxic than menthol to the rice weevil. Different modes of toxicity of these monoterpenes towards S oryzae are discussed. © 2001 Society of Chemical Industry     

Synergism of teflubenzuron and chlorfluazuron in an acylurea-resistant field strain of Plutella xylostella L. (lepidoptera: Yponomeutidae)

Topical application of the synergists piperonyl butoxide (PB) and S,S,S-tributyl phosphorotrithioate (DEF) to second-instar larvae of a standard laboratory strain (FS) and an unselected Malaysian field strain (CH) of the diamondback moth Plutella xylostella had no significant effect on the toxicity of the acylurea insecticides, chlorfluazuron and teflubenzuron, in a subsequent leafdip bioassay. In contrast, pre-treatment with PB or DEF in acylurea-selected subpopulations of the CH strain with varying levels of cross-resistance to chlorfluazuron and teflubenzuron significantly increased (up to 34-fold and 28-fold, respectively) the toxicity of both compounds, suggesting that microsomal monooxygenases and esterases may be involved in resistance. The addition of a mineral oil, ‘Sunspray 6E’, to topically-applied chlorfluazuron consistently reduced its LD₅₀ value, and the effect of the oil appeared to be greatest on the most resistant population of P. xylostella. However, the effects of the oil were not significant (P > 0·05) and further studies are necessary to determine whether a penetration factor is present in the CH strain.     

Uptake of aminotriazole from humectant-surfactant combinations and the influence of humidity

Uptake of aminotriazole (3-amino-1,2,4-triazole) by bean leaves (Phaseolus vulgaris var. Canadian Wonder) was not greatly influenced by the addition to the spray solution of dimethylformamide (DMF), ethylene glycol and polypropylene glycol 400 (PPG 400) over the concentration range 1.0–50.0 ml litre^?1. However, the addition of polyoxyethylene 20 sorbitan monolaurate (polysorbate 20) (0.2–1.0 g litre^?1) to spray solutions of the above additives and glycerol (5.0 ml litre^?1; except for DMF, 50.0 ml litre^?1) substantially increased uptake to 80–100% in all cases at 50 ± 10% relative humidity (r.h.). Similar penetration figures were recorded when a range of polysorbate surfactants (polysorbate 20, 40, 60, 80 and 85; 0.2 g litre^?1) were applied to spray solutions containing either dimethyl sulphoxide (DMSO) or glycerol (5.0 ml litre^?1). Humidity was found to have a critical effect upon the humectant-surfactant combinations tested, i.e. DMSO + polysorbate 20, ethylene glycol+ polysorbate 20 and PPG + 400-polysorbate 20 (5.0 ml litre^?1+0.2 g litre^?1). With DMSO + polysorbate 20 the following uptake figures were recorded: < 30% r.h., 3.1 %; 45 ± 10% r.h., 86.8%; 55–65% r.h., 48.2 % and 100% r.h., 0.3%. Similar trends were recorded with all three humectant-surfactant combinations. Further studies revealed that the adverse effect of humidity on DMSO-polysorbate mixtures could be at least overcome partially by regulating the DMSO concentration.     

Effects of buprofezin and diflubenzuron on various developmental stages of Asian citrus psyllid, Diaphorina citri

BACKGROUND: Diaphorina citri populations in Florida are developing resistance to commonly used neurotoxic insecticides. Alternatives to neurotoxins, such as insect growth regulators, are needed to control this season-long subtropical pest to prevent or delay development of insecticide resistance. In the present investigation, two insect growth regulators (IGRs), buprofezin and diflubenzuron, were evaluated against various developmental stages of D. citri. RESULTS: The 0–1-day-old D. citri eggs were more susceptible to buprofezin and diflubenzuron than the 3–4-day-old eggs. Adult emergence was completely suppressed by treating first- or third-instar nymphs with buprofezin or diflubenzuron at 30–240 or 23–184 µg mL⁻¹ rates respectively. Treatment of fifth-instar nymphs with diflubenzuron at a rate of 184 µg mL⁻¹ and with buprofezin at 30–240 µg mL⁻¹ rates resulted in approximately 20 and 15–80% reductions in adult emergence respectively. The mean number of eggs per plant was reduced at 5 days after topical treatment with diflubenzuron. Mean egg hatch per plant was reduced at 5 and 6–15 days after topical treatments with buprofezin and diflubenzuron respectively. CONCLUSION: Buprofezin and diflubenzuron effectively suppressed D. citri adult emergence. D. citri were more susceptible as early (first–third-instar) than late (fifth-instar) nymphs. Both IGRs inhibited egg production and egg hatch. Reduction in the number of subsequent offspring suggests reduced vertical transmission of Candidatus Liberibacter asiaticus, the pathogen thought to cause citrus greening disease. The present results indicate that both IGRs tested here should be effective tools for rotation in insecticide-based D. citri management programs. Copyright © 2012 Society of Chemical Industry     

Laboratory Evaluation of the Novel Naturally Derived Compound Spinosad against Ceratitiscapitata

Laboratory studies were conducted to determine the effect of the naturally derived compound spinosad on Ceratitis capitata Wied. (Diptera, Tephritidae). The organophosphate fenthion was used as a standard. Direct dose-dependent mortality and reduced fecundity were observed in oral treatment of adults with spinosad. The LC₉₀ values 14 h and seven days after treatment were 19·50 and 0·49 mg litre⁻¹ respectively. Fenthion was less active (the LC₅₀ eight days after treatment was 1·17 mg litre⁻¹) and did not affect the fecundity of the fly. Adults were also very susceptible to spinosad and fenthion via residual contact. For spinosad, 100% mortality was recorded 48 h after treatment for a dose of 10 mg litre⁻¹. Spinosad was more effective than fenthion in suppressing larval development when neonate larvae were reared on treated diet supplemented with a range of concentrations from 0·02 to 0·83 mg kg⁻¹ diet. Last-instar larvae were much less susceptible to spinosad or fenthion when exposed via dipping or when they pupated in treated medium and both products had similar performance. A lack of ovicidal activity was observed in direct egg-treatments with spinosad but significant reductions from 1 mg litre⁻¹ onwards were recorded for fenthion.     

Sensitivity of European Plasmopara viticola populations to cymoxanil

Between 1995 and 1997, 278 grape downy mildew (Plasmopara viticola) populations originating from European vineyards were characterised for their sensitivity to cymoxanil in a leaf-disc assay. The sensitivity profile revealed a wide distribution, with minimum inhibitory concentrations (MIC) ranging from 10 to more than 800 mg litre⁻¹. EC₅₀ values ranged from 1 to more than 800 mg litre⁻¹ with an average of 125 mg litre⁻¹. The sensitivity distribution was stable between 1995 and 1997. Surprisingly, populations from Portugal appeared significantly more sensitive than those from France or Italy, which could not be linked to differential cymoxanil usage in these countries. P viticola populations collected outside Europe and never exposed to cymoxanil appeared significantly more sensitive than exposed European populations, with an average EC₅₀ value of 10 mg litre⁻¹. The level of sensitivity of European P viticola populations was relatively unaffected by the number of cymoxanil applications made during a season or by the number of years of cymoxanil use. No link was found between the level of sensitivity in the leaf-disc assay and the level of performance of the cymoxanil mixtures used in the fields where the populations originated. Specific field trials conducted in Italy and Portugal have shown that the performance of cymoxanil-based mixtures remained good even on populations of the grape downy mildew fungus characterised as less sensitive in the leaf-disc assay. While there are no baseline sensitivity data for pre-commercialisation P viticola populations, the results of our study suggest that a shift in sensitivity (12.5-fold) may have occurred in some areas since introduction of cymoxanil on grapes nearly 20 years ago. Because cymoxanil is never used alone, it is difficult to determine whether or not practical resistance is occurring in European vineyards. © 1999 Society of Chemical Industry     

A laboratory evaluation of the effectiveness of diflubenzuron against Dermestes maculatus De Geer and other storage insect pests

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.     

The mode of action of RH‐1965: a new phenylpyrimidinone bleaching herbicide

RH‐1965 is a new bleaching herbicide which causes newly developing leaf tissue to emerge devoid of photosynthetic pigments. Mode‐of‐action studies revealed that RH‐1965 inhibited the accumulation of both total chlorophyll and β‐carotene. Concomitantly, it induced the accumulation of the β‐carotene precursors, phytoene, phytofluene and, in particular, ξ‐carotene. Inhibition of chlorophyll accumulation by RH‐1965 is attributed to the photo‐oxidative destruction of chlorophyll in the absence of β‐carotene because RH‐1965 blocked chlorophyll accumulation to a greater extent under high light (50–330 µE m⁻² s⁻¹) than under low light (0.8 µE m⁻² s⁻¹) conditions. Radish (Raphanus sativus L) and barnyardgrass (Echinochloa crus‐galli (L) Beauv) were very senstive to RH‐1965. Under high light (330 µE m⁻² s⁻¹), the I₅₀ values for inhibition of chlorophyll accumulation were 0.10 and 0.15 µM , respectively. Wheat (Triticum aestivus L), on the other hand, was much less sensitive to RH‐1965 (I₅₀ = 1.4 µM ). It is concluded that the mode of action of RH‐1965 involves the inhibition of ξ‐carotene desaturation. © 2000 Society of Chemical Industry     

Residues of diflubenzuron on horse chestnut (Aesculus hippocastanum) leaves and their efficacy against the horse chestnut leafminer, Cameraria ohridella

Residues of the insect growth regulator diflubenzuron were quantified on horse chestnut (Aesculus hippocastanum L.) leaves treated with a diflubenzuron 480 g litre^?1 SC, Dimilin. To analyse the samples, an analytical procedure was developed involving a simple extraction step followed by high‐performance liquid chromatography on an octadecyl‐modified silica column with methanol + 0.01 M ammonium acetate mobile phase. The results showed diflubenzuron to be highly stable on horse chestnut leaves; more than 4 months (127 days) after application, 38% (on average) of the insecticide still remained on/in the leaves. The data confirmed biological observations showing diflubenzuron's long‐term efficacy against the horse chestnut leafminer, Cameraria ohridella Deschka & Dimi?, which is the most important pest of the horse chestnut in Europe. The hypothesis of possible penetration of diflubenzuron into the leaf mass is explored and discussed. Copyright © 2006 Society of Chemical Industry     

Diflubenzuron: Some aspects of its ovicidal and larvicidal mode of action and an evaluation of its practical possibilities

Diflubenzuron, 1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)urea, possesses larvicidal and ovicidal activities. On larvae it acts mainly as a stomach poison, yet it sometimes exhibits important contact activity. Though all instars can be controlled, older instars are generally less susceptible than younger ones. Histological inspections of Leptinotarsa decemlineata larvae revealed that after ending exposure to the compound, distortions in newly deposited cuticular layers decreased gradually. Ovicidal effects resulted from direct contact of diflubenzuron with eggs or from contamination of females by contact or feeding. Electron microscopic observations of embryos of Leptinotarsa decemlineata, contaminated via the female, also showed disturbed cuticule formation, suggesting a similar activity of the compound in larvae and in eggs. Spraying the eggs of Leucoptera scitella shows the compound to be mainly ovidical at a rate of 100 mg litre^?1, whilst with lower concentrations (10 and 1 mg litre^?1) the young larval instar will be killed. The levels of cross-resistance to diflubenzuron as a larvicide are low and the compound can be used effectively in the field against populations that are highly resistant to conventional insecticides. Laboratory and field results, based on larvicidal and ovicidal activities of diflubenzuron, are discussed in respect of species belonging to the Diptera, Lepidoptera, Coleoptera, Acarina (Phyllocoptruta oleivora) and Hemiptera (Eurydema oleraceum and Psylla piri).     

Pharmacokinetics of sulfluramid and its metabolite desethylsulfluramid after intravenous and intraruminal administration of sulfluramid to sheep

Pharmacokinetic properties and tissue residues of the insecticide sulfluramid (I) and its major metabolite desethylsulfluramid (II) were determined in healthy sheep after bolus intravenous (IV) administration (5 and 15 mg kg⁻¹; n = 10) and bolus intraruminal (IR) administration (100 and 400 mg kg⁻¹; n = 12) of I . Depression, lethargy, and dyspnea were noted for 4 h after the higher IV dose, but not after the other IV or IR doses. The time courses of the mean blood concentrations of I and II were best described by a two-compartment open model with rapid distribution and slow elimination phases. The blood-to-plasma concentration ratios for I and II were 1.43 (± 0.50) and 26.7 (± 9.41), respectively, suggesting binding of II to red blood cells. The T_1/2β values for I and II for the higher IV dose of I were 15.3 (± 4.68) h and 63.4 (± 4.75) h and for the higher IR dose of I , 31.5 (± 5.41) h and 74.9 (± 7.49) h, respectively. Bioavailability was 28.6 (± 2.96)% for the lower IR dose and 19.5 (± 0.99)% for the higher IR dose. C_max values for II were higher in female than male sheep after IR administration of I . Only II was found in tissue samples, with the highest concentration being in liver (9.4 (± 5.2) µg g⁻¹). © 1999 Society of Chemical Industry     

Morphogenetic effects of diflubenzuron,an inhibitor of chitin deposition,on the coconut black-headed caterpillar (Nephantis serinopa myer)

Feeding the last instar larvae of Nephantis serinopa, the coconut black-headed caterpillar, on coconut leaves that had been dipped in diflubenzuron suspensions (0.2-4.0 g litre^?1) and dried, inhibited the moulting process and caused morphogenetic deformities of their pupae. The inhibition of moulting ranged from 27.5 to 75% The maximum effect was produced by suspensions of 4.0 g litre^?1 when only 5% of the larvae survived to become adults against 97.5% of untreated larvae.