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.     

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.     

Activity of abamectin against larval stages of Spodoptera littoralis boisduval and Heliothis armigera hübner (Lepidoptera: Noctuidae) and possible mechanisms determining differential toxicity

Marked changes in the relative toxicity of topically-applied abamectin were found between larval instars of Spodoptera littoralis, toxicity decreasing up to the fifth instar but increasing over 500-fold (at LD₅₀ level) in the sixth instar. By contrast, the toxicity of abamectin remained constant from fifth to sixth instar Heliothis armigera and there was an increase in the toxicity of two chemically unrelated insecticides, malathion (4-fold) and lambda-cyhalothrin (2.5-fold), from fifth to sixth instar S. littoralis. Prior topical application or injection of the microsomal oxidase inhibitor, piperonyl butoxide (PB) increased the toxicity of abamectin (6–8 and 16-fold respectively) against fifth instar S. littoralis, while topically-applied PB increased the proportion of radioactivity present as abamectin in the ventral nerve cord of this instar following topical application with [³H]abamectin. Topically-applied PB also enhanced the toxicity of abamectin against third (4-fold) and fourth instar (5-fold) S. littoralis but had no significant effect on sixth instar S. littoralis, fifth instar H. armigera, or on the toxicity of malathion and lambda-cyhalothrin against fifth instar S. littoralis. Topical application of the esterase inhibitor, S,S,S-tributyl phosphorothioate (DEF) significantly increased the toxicity of abamectin at the LD₅₀ level (3-fold) against fifth instar S. littoralis. The toxicity of injected abamectin against fifth instar S. littoralis was greater (20-fold) than with topical application but injected abamectin was less toxic (2-fold) against sixth instar S. littoralis and had no significant effect on fifth instar H. armigera. It is suggested that differential toxicity of abamectin is due in part to greater metabolism and reduced penetration in fifth instar S. littoralis than in sixth instar S. littoralis or fifth instar H. armigera.     

Effect of the acylurea insect growth regulator teflubenzuron on the endo-larval stages of the hymenopteran parasitoids Cotesia plutellae and Diadegma semiclausum in a susceptible and an acylurea-resistant strain of Plutella xylostella

The toxicity of the acylurea, teflubenzuron, was assessed against larval stages of the hymenopteran parasitoids, Cotesia plutellae Kurdjumov and Diadegma semiclausum Hellén in a susceptible laboratory strain and a teflubenzuron-resistant field strain of the diamondback moth, Plutella xylostella L. In fourth-instar hosts (L4), when both parasitoid species were in their final larval instar, teflubenzuron significantly (P < 0.05) reduced emergence of adult D. semiclausum but had no significant (P > 0.05) effect on C. plutellae, although a small proportion of the latter were unable to reproduce. Treatment of L4 hosts with teflubenzuron ( > LD₅₀) had no significant (P > 0.05) effect on the fecundity of surviving females of D. semiclausum. Similar differential toxicity with teflubenzuron was observed in L2 hosts, when parasitoids were at the egg or early larval instar stage. There was no apparent increased effect of teflubenzuron on either species of parasitoid when highly resistant (c. 4000-fold) L2 hosts (field strain) were treated with concentrations of teflubenzuron two to three orders of magnitude greater than in equivalent experiments with the susceptible host strain. This suggests that host resistance to teflubenzuron confers some protection to both species of parasitoid. Uptake experiments with [¹⁴C]teflubenzuron showed that accumulation of radioactivity was much greater in D. semiclausum than in C. plutellae and this may account for the differential toxicity observed. The results are discussed in relation to the field status of these parasitoid species. The influence of insecticide resistance in the host on endo-larval parasitoids is also considered.     

The effect of pretreatment with S,S,S-tributyl phosphorotrithioate on deltamethrin resistance and carboxylesterase activity in Aphis gossypii (Glover) (Homoptera: Aphididae)

The synergism of S,S,S-tributyl phosphorotrithioate (DEF) and its effect on carboxylesterase activity were investigated in deltamethrin-selected resistant (DRR) and susceptible (DSS) strains of cotton aphids, Aphis gossypii (Glover). Compared to the DSS strain, the DRR strain showed 23,900-fold resistance to deltamethrin, and 7560- and 99-fold cross-resistance to bifenthrin and ethofenprox, respectively. The synergist, DEF, increased the toxicity of both deltamethrin and bifenthrin, but not of ethofenprox when DEF was pretreated of 15 h. DEF exhibited significant inhibition on the carboxylesterase activity in the DRR strain, but no significant effect on that of the DSS strain in vitro. After the cotton aphids exposing to DEF, the carboxylesterase activity decreased gradually until 15 h and then gradually recovered until 24 h in the DRR strain, which fluctuated according to the effect of DEF on the deltamethrin toxicity detected using DEF pretreatment in the DRR strain. Therefore, our studies suggested that the effect of DEF on carboxylesterase was associated with deltamethrin resistance in the DRR strain.     

Comparative studies on acylurea insect growth regulators and neuroactive insecticides for the control of the armyworm Spodoptera exempta walk

Leaf-dip bioassays with commercial pesticide formulations were used throughout this study. Third-instar larvae of Spodoptera littoralis were bioassayed for comparative purposes. The end-point mortality against the third-instar larvae (L3) of two Spodoptera exempta populations (Bangor and Gent) and a S. littoralis population (NRI) was found to occur at 72 h and 120 h for neuroactive compounds (carbamate, organophosphate and pyrethroid insecticides) and acylureas respectively. Overall, the acylureas were found to be more toxic (up to 240-fold at the LC₅₀ level) than the most active of the neuroactive compounds tested, the pyrethroids. This difference was greatest against S. littoralis, which was markedly less sensitive to the latter compounds. The Gent population of S. exempta was also found to be significantly less sensitive (7-folt at LC₅₀) to the pyrethroid, lambda-cyhalothrin, than the Bangor strain. Two of the most toxic neuroactive and non-neuroactive compounds, the pyrethroid, cypermethrin and the acylurea, teflubenzuron were chosen for further studies with S. exempta (Gent) and S. littoralis. Relatively little difference in the toxicity of teflubenzuron was observed against different larval instars (L2, L3 and L4) of S. exempta when compared with cypermethrin. Choice-chamber-experiments on feeding behaviour showed that when L3 larvae of either species were exposed to both treated and untreated leaves. teflubenzuron had no significant effect on larval distribution, the percentage of each leaf disc consumed or larval weight gain when compared with untreated controls. In contrast, a marked dose-dependent repellent response to cypermethrin-treated leaves was shown by S. littralis after 6 h. together with corresponding reductions in the percentage of the treated leaf consumed and in larval weight gain. Similarly, when L3 S. exempta were exposed only to pesticidetreated leaves, cypermethrin significantly reduced premoult larval weight gain, whereas tefiubenzuron had no premoult effect. However, following exposure of L3 S. exempta and S. littoralis to teflubenzuron for 48 h prior to moulting, L4 which survived the moult showed reduced weight gain compared with controls, the reduction being more pronounced on maize than on artificial diet. This antifeedant effect increased in proportion to the concentration of teflubenzuron originally administered. The effect of exposure time to teflubenzuron was examined by placing L3 S. exempta and S. littoralis on leaves treated with the approximate LC₅₀ or LC₉₅ dose for 6–48 h. The exposure time required to produce appreciable mortality (relative to LC values) within the treated population was found to be 24 h.     

Aqueous solubilities,photolysis rates and partition coefficients of benzoylphenylurea insecticides

The aqueous solubilities and octanol–water partition coefficients (K_OW) of the benzoylphenylurea (BPU) insecticides teflubenzuron, chlorfluazuron, flufenoxuron and hexaflumuron were determined in comparison with the more extensively studied diflubenzuron. Both teflubenzuron and hexaflumuron were substantially less water‐soluble (9.4 (± 0.3) µg litre⁻¹ and 16.2 (± 0.5) µg litre⁻¹ in water, respectively) than the value previously reported for diflubenzuron (89 (± 4) µg litre⁻¹ in water). Log K_OW values for diflubenzuron, teflubenzuron, hexaflumuron, flufenoxuron and chlorfluazuron were 3.8, 5.4, 5.4, 6.2 and 6.6, respectively, as determined using reverse‐phase HPLC. Photodegradation of hexaflumuron, teflubenzuron and diflubenzuron in water indicated hexaflumuron to be the most rapidly degraded of the three compounds at pH 7.0 (t_1/2 = 8.6 (± 0.4) h) and pH 9.0 (t_1/2 = 5 (± 1) h); diflubenzuron was the slowest of the three pesticides to degrade in pH 7.0 (17 (± 4) h) and pH 9.0 (8 (± 2) h) buffered water. In a solar simulator using river water buffered to pH 9.0, teflubenzuron, hexaflumuron and diflubenzuron half‐lives were 20 (± 4), 15 (± 2) and 12 (± 1) h, respectively; dark controls showed no loss of parent BPU over similar time periods. © 2000 Society of Chemical Industry     

Communication to the Editor Insecticide Resistance in a Strain of Aphis gossypii from Southern France

A strain (R) of Aphis gossypii from Southern France was found to be resistant to several insecticides, particularly to pirimicarb, as compared to a susceptible strain (S). Resistance levels were determined by biological tests, and the highest resistance factor (1350) was for pirimicarb. Resistance was mainly restricted to anticholinesterase inhibitors. Use of synergists, DEF and PB, suggested that resistance mechanisms based on detoxification were involved to a minor extent, since a good correlation was observed between I₅₀ values and k_i values of AChE and in-vivo bioassay data. The two strains differed in esterase activity, with a 27·7-fold increase in the R strain. Resolution of esterases by polyacrylamide gel electrophoresis showed different patterns in the S and R strains, and two isozymes were less sensitive to pirimicarb in the S strain; however, no in-vitro degradation of [¹⁴C]pirimicarb was observed. These data suggest that the main mechanism of resistance was through a decrease in the sensitivity of the target, AChE, to the insecticides. © 1997 SCI.     

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.     

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.     

The response of pyriproxyfen-resistant and susceptible Bemisia tabaci Genn (Homoptera: Aleyrodidae) to pyriproxyfen and fenoxycarb alone and in combination with piperonyl butoxide

Pyriproxyfen was effective against susceptible Bemisia tabaci eggs at a LC₅₀ of 0.003 mg litre⁻¹ and against nymphs at 0.02 mg litre⁻¹. In comparison, eggs of a laboratory selected, pyriproxyfen-resistant B tabaci strain, originating in an Israeli greenhouse, exhibited 6500-fold resistance and nymphs exhibited 1100-fold resistance. Eggs and nymphs of a strain from an Israeli sunflower field exhibited 450 and 210-fold resistance in comparison to the susceptible standard. Fenoxycarb was generally less effective than pyriproxyfen against B tabaci eggs and nymphs but was unaffected by pyriproxyfen resistance. Piperonyl butoxide (PB) was antagonistic to pyriproxyfen, and this increased with increasing pyriproxyfen resistance. PB had no effect on the toxicity of fenoxycarb. Collectively, these data imply that the modes of action of pyriproxyfen and fenoxycarb are distinct, despite the structural similarities of these molecules. Possible reasons for the antagonism of PB against pyriproxyfen are discussed. © 1999 Society of Chemical Industry     

广州、深圳地区小菜蛾对定虫隆、Bt的抗性监测

采用 Potter's 喷雾塔喷雾的方法测定广州和深圳菜区小菜蛾对儿丁质合成抑制剂定虫隆、氟虫脲、伏虫隆、氟铃脲的抗药性。结果表明,深圳菜区小菜蛾对定虫隆产生明显抗性,1990年11月测定抗性倍数为15.0,1991年12月为70.9,对氟虫脲、伏虫隆、氟铃脲具有不同程度交互抗性,抗性倍数分别为26.7,15.5 和5.8。广州菜区小菜蛾对以上药剂均未产生抗性(抗性倍数最高为2.8)。采用浸渍法测定小菜蛾对苏云金杆菌 Bt 抗性的结果表明,深圳菜区小菜蛾对 Bt 的抗性逐年提高,1990年12月测定的抗性倍数为21.1,1991年12月为26.9,1992年3月为35.0,广州菜区小菜蛾具有强的耐药性或低抗药性,抗性倍数8—9。     

小菜蛾对阿维菌素的抗性选育及交互抗性研究

用阿维菌素对小菜蛾进行室内抗性汰选,选择压为约杀死种群70％的剂量。连续施药7～8次即表现抗性趋势,汰选至11代,获得抗性指数为80.71的抗性种群(ABM-R)。ABM-R种群对所测试的有机磷杀虫剂乙酰甲胺磷、有机氯类的硫丹、沙蚕毒素类的杀螟丹、氨基甲酸酯类的灭多威、微生物杀虫剂Bt、磺胺脲类衍生物丁醚脲、芳基取代的吡咯杂环化合物虫螨腈和昆虫生长调节剂定虫隆、虫酰肼无交互抗性(R/S为0.73～1.19),而对苯基吡唑类氟虫腈的敏感性却有所上升(R/S为0.22)。增效剂试验显示,PB和唧对ABM-S种群无增效作用,而对ABM-R种群增效作用显著,增效比分别为24.57和13.61,表明多功能氧化酶和羧酸酯酶在抗性机制中可能起重要作用。     

Pesticide interactions: Effects of organophosphorus pesticides on the metabolism,toxicity, and persistence of selected pyrethroid insecticides

The organophosphorus pesticides profenofos, sulprofos, O-ethyl O-(4-nitrophenyl) phenylphosphonothioate (EPN), and S,S,S,-tributyl phosphorotrithioate (DEF) administered intraperitoneally to mice at 0.5 to 5 mg/kg strongly inhibit the liver microsomal esterase(s) hydrolyzing trans-permethrin. Profenofos, EPN, and DEF at 25 mg/kg increase the intraperitoneal toxicity of fenvalerate > 25-fold and of malathion > 100-fold. Topically applied profenofos, sulprofos, and DEF significantly synergize the toxicity of cis-cypermethrin to cabbage looper larvae and house fly adults but these phosphorus compounds are much less effective in synergizing the toxicity of trans-permethrin. The magnitude of synergism appears to depend on the species, organophosphorus compound, and pyrethroid involved. Profenofos, sulprofos, and EPN do not significantly alter the persistence of trans-permethrin on bean foliage.     

甜菜夜蛾敏感品系的获得及其对12种杀虫剂的敏感基线

以高效氯氰菊酯为筛选药剂,通过室内单对汰选获得了甜菜夜蛾敏感品系,并采用浸叶法和点滴法测定该敏感品系对甲氨基阿维菌素苯甲酸盐、氯虫苯甲酰胺等12种常用药剂的敏感基线。浸叶法测得该品系对供试药剂的敏感性由高到低依次为:甲氨基阿维菌素苯甲酸盐(LC50为0.0340 mg/L)、茚虫威、氟啶脲、甲氧虫酰肼、氯虫苯甲酰胺、氟虫双酰胺、高效氯氰菊酯、虫酰肼、多杀菌素、毒死蜱、虫螨腈、灭多威(124.0482mg/L)。点滴法测得12种杀虫剂LD50由小到大依次为:高效氯氰菊酯、茚虫威、甲氧虫酰肼、甲氨基阿维菌素苯甲酸盐、虫酰肼、毒死蜱、多杀菌素、氯虫苯甲酰胺、虫螨腈、氟虫双酰胺、灭多威、氟啶脲。结果表明,该敏感基线可用于甜菜夜蛾的抗药性监测。     

Resistance of <Emphasis Type="BoldItalic">Spodoptera exigua</Emphasis> to ten insecticides in Shandong,China

Spodoptera exigua (Hübner) collected from three regions (two scallion-producing regions and one ginger-producing region) in Shandong, China and a laboratory colony of Wuhan (WHLC) were evaluated for their susceptibilities to ten insecticides (emamectin benzoate, chlorfenapyr, indoxacarb, spinosyn, tebufenozide, methoxyfenozide, chlorfluazuron, beta-cypermethrin, chlorpyrifos and methomyl) in 2008, 2009 and 2010 using a leaf-dip bioassay method. The results indicate that the resistance ratios of S. exigua to newer insecticides such as emamectin benzoate, chlorfenapyr and indoxacarb were all below 20-fold, with no obvious change in all 3 years. S. exigua exhibits moderate resistance to spinosyn, and its resistance ratios increased from 1.98–5.31-fold in 2008 to 14.31–64.20-fold in 2010 from three regions as compared with WHLC. S. exigua showed moderate to high resistance to insect growth regulators such as tebufenozide, methoxyfenozide, chlorfluazuron in 2008, 2009 and 2010, in which resistance to chlorfluazuron was rapidly increased from 31.49–88.19-fold in 2008 to 1184.39–2789.67-fold in 2010. Resistance of S. exigua to beta-cypermethrin and chlorpyrifos varied greatly among the three regions, ranging from 95.31–437.97-fold and 25.05–40.64-fold in 2008, 951.81–1304.40-fold and 44.91–186.33-fold in 2009, to 27.27–1095.31-fold and 19.12–267.98-fold in 2010. In contrast, S. exigua showed low resistance to methomyl, and the resistance ratio was below 5-fold in 3 years. There are several reasons accounting for varying degrees of resistance, including selection pressure, cropping structure and migration, in which the migration of S. exigua may play an important role.     

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.     

Multiple Resistance in the Larger House Fly Musca domestica in Germany

Populations of the housefly Musca domestica isolated from farms in different German districts with strong resistance problems were compared to laboratory strains with varying resistance spectra. Resistance against pyrethroids, organophosphates and carbamates was tested using impregnated filter papers, and by topical application using a susceptible housefly strain (origin WHO) for comparison. The multi-resistant fly strains tested had a strong resistance against these insecticide groups, ranging from 37- to >10000-fold for organophosphates and 150- to >6600-fold for pyrethroids. The constituent enantiomer pairs of the α-cyano-pyrethroid cyfluthrin were tested, as was beta-cyfluthrin. With respect to multi-resistant fly strains, the isomers II and IV had the best activity, with LD₅₀ values of 0·012 and 0·014 μg per fly, respectively. In addition, different groups of insect growth regulators (juvenile hormone analogues, chitin synthesis inhibitors and one triazine derivative) were tested in a special larvicidal test. The chitin synthesis inhibitors were quite effective against multi-resistant M. domestica strains except for one strain with strong resistance against chitin synthesis inhibitors, developed after extensive treatments with benzoylphenylureas for several years. The fly strains tested were not resistant against cyromazine. Additionally, the insecticides were combined with the synergists piperonyl butoxide, tributylphosphorotrithioate (DEF) and Cibacron blue and tested against the fly strain with the strongest resistance spectrum (‘Grimm’) in comparison to the susceptible strain (‘WHO-N’). Piperonyl butoxide had the greatest effect on the efficacy of cyfluthrin followed by Cibacron blue and DEF. In a parallel investigation with susceptible and resistant house fly strains, different enzyme activities related with resistance mechanisms were tested, e.g. glutathione S-transferase (3·5-fold) and mixed-function oxidase (2·3-fold). Implications of these results for management of insecticide resistance in M. domestica are discussed.     

Cross-resistance and biochemical mechanisms of abamectin resistance in the western flower thrips, Frankliniella occidentalis

Abamectin resistance was selected in the western flower thrips [Frankliniella occidentalis (Pergande)] under the laboratory conditions, and cross-resistance patterns and possible resistance mechanisms in the abamectin-resistant strain (ABA-R) were investigated. Compared with the susceptible strain (ABA-S), the ABA-R strain displayed 45.5-fold resistance to abamectin after 15 selection cycles during 18 generations. Rapid reversion of abamectin resistance was observed in the ABA-R strain in the absence of the insecticide selection pressure. Moderate and low levels of cross-resistance to chlorpyrifos (RR 11.4) and lambda-cyhalothrin (3.98) were observed in the ABA-R strain, but no significant cross-resistance was found to spinosad (2.00), acetamiprid (1.47) and chlorfenapyr (0.26). Our studies also showed that the esterase inhibitor S,S,S-tributyl phosphorotrithioate (DEF) and glutathione S-transferase inhibitor diethyl maleate (DEM) were not able to synergize the toxicity of abamectin, whereas the oxidase inhibitor piperonyl butoxide (PBO) conferred a significant synergism on abamectin in the ABA-R strain (SR 3.00). Biochemical analysis showed that cytochrome P450 monooxygenase activity of the ABA-R strain was 6.66-fold higher than that of the ABA-S strain. It appears that enhanced oxidative metabolism mediated by cytochrome P450 monooxygenases was a major mechanism for abamectin resistance in the western flower thrips.     

Comparative toxicity of two ecdysteroid agonists,RH-2485 and RH-5992, on susceptible and pyrethroid-resistant strains of the Egyptian cotton leafworm,Spodoptera littoralis

The comparative toxicity of two non-steroidal ecdysteroid agonists, RH-2485 and RH-5992 (tebufenozide), on development stages, fecundity and egg viability of a susceptible laboratory strain and a pyrethroid-resistant field strain ofSpodoptera littoralis (Boisduval) was evaluated. Taking the LC₅₀s as the criterion, RH-2485 was 3–7-fold more potent than RH-5992 against the susceptible and 7–14-fold more against the field strain. The LC₅₀ of RH-2485 in the 1st and 6th instars of the susceptible strain was 0.32 and 0.57 mg a.i./l, respectively. The field strain showed a mild cross-resistance of about threefold to both compounds in 1st instars and to a lesser extent in 6th instars. A considerable increase in fecundity (~3-fold) and no effect on egg viability was observed when 6th instars were fed on cotton leaves treated with 0.25 mg a.i./l RH-2485 (~LC₄₀). Our results indicate that both compounds are potentially potent insecticides for controllingS. littoralis larvae, being 10-60-fold more potent than a previous ecdysteroid agonist, RH-5849.