Field and laboratory tests of new insecticides against the apple maggot, Rhagoletis pomonella (Walsh) (Diptera: Tephritidae)

Laboratory bioassays and field tests were conducted to compare the effectiveness of the new insecticides, imidacloprid, indoxacarb, pyriproxyfen, spinosad, thiacloprid, and thiamethoxam, against apple maggot. The activity ranking of the compounds in reducing oviposition in laboratory bioassays was: imidacloprid, 95% reduction at 11 ppm > thiamethoxam, 91% and thiacloprid, 89% reduction at 100 ppm > spinosad, 98% reduction at 316 ppm > indoxacarb, 80% reduction at 1000 ppm > pyriproxyfen, 0% reduction at 38 ppm. In laboratory bioassays, the only insecticides that were toxic to flies at concentrations equal to or below the recommended field rates were imidacloprid, (50% of flies at 11 ppm), spinosad (90% of flies at rates > 10 ppm), and thiamethoxam (approximately 50% of flies at 32 ppm). In field trials, thiacloprid was the only material that consistently controlled apple maggot fruit infestation that was comparable to standard treatments of organophosphate insecticides. Spinosad applied at weekly intervals, and indoxacarb applied as biweekly sprays provided adequate control of apple maggot damage when infestation levels in the field were low, but were not effective in preventing damage in small plots when apple maggot pressure was high.     

Development, oviposition, and mortality of Neoseiulus fallacis (Acari: Phytoseiidae) in response to reduced-risk insecticides

Eight reduced-risk insecticides (acetamiprid, thiamethoxam, imidacloprid, thiacloprid, methoxyfenozide, pyriproxyfen, indoxacarb, and spinosad) and three conventional insecticides (azinphosmethyl, fenpropathrin, and esfenvalerate) were tested against Neoseiulus fallacis (Garman) (Acari: Phytoseiidae), the most abundant predacious mite in North Carolina apple (Malus spp.) orchards. To assess the effect of insecticides on development and mortality of N. fallacis immatures, 12-h-old eggs were individually placed on bean leaf disks previously dipped in insecticide solutions. Tetranychus urticae Koch (Acari: Tetranychidae) females were added as a food source. None of the reduced-risk insecticides significantly affected immature N. fallacis compared with the control; however, the pyrethroids esfenvalerate and fenpropathrin were highly toxic to immatures. To evaluate the effect of insecticides on mortality and oviposition of adult N. fallacis, 7- to 8-d-old females were confined on insecticide-treated bean leaves with Malephora crocea (Aizoaceae) pollen added as a food source. Spinosad resulted in the highest mortality, whereas azinphosmethyl, acetamiprid, fenpropathrin, and imidacloprid were moderately toxic, and mortality from esfenvalerate, indoxacarb, thiacloprid, methoxyfenozide, pyriproxyfen, and thiamethoxam did not differ significantly from the control. Oviposition was affected in a similar manner, with the exception of acetamiprid that did not affect oviposition, and thiamethoxam that reduced oviposition.     

Characterization of nicotinic acetylcholine receptors from the insects Aphis craccivora, Myzus persicae, and Locusta migratoria by radioligand binding assays: relation to thiamethoxam action

Thiamethoxam, a new neonicotinoid insecticide acting at nicotinic acetylcholine receptors, was characterized in competition binding assays with [3-H]-imidacloprid, a specific nicotinic ligand, using membranes from the aphids Aphis craccivora and Myzus persicae, and from the locust Locusta migratoria. In all insects, Scatchard analysis suggested two binding sites for imidacloprid with Kd values in the range of 1 nM and 10 nM, respectively. The Hill values were significantly below 1 (range of 0.63 to 0.85). In contrast to imidacloprid and nicotine, the potency of thiamethoxam to displace [3-H]-imidacloprid varied considerably among these insects. Thiamethoxam was more active than nicotine on Aphis receptors but 100-fold less in Locusta, a nontarget insect. Comparable relations were found to nithiazine. In Myzus, the inhibition curve for thiamethoxam was shallow. This suggested a heterogeneous receptor population displaying a range of binding affinities to thiamethoxam in this aphid. In all three insects, the other neonicotinoid insecticides studied competed with [3-H]-imidacloprid in the same order: thiacloprid > imidacloprid > or = acetamiprid > nitenpyram. N-Methylation of imidacloprid strongly reduced the affinity to the imidacloprid site, whereas N-demethylation of thiamethoxam resulted in a comparable increase of affinity. Supplementary assays were performed with (-)-[3-H]-nicotine and [3-H]-alpha-bungarotoxin on locust membranes. Overall, the data suggested that the outstanding insecticidal properties of thiamethoxam may be due to either a different binding site on nicotinic receptors, or receptor isoforms, or specific pharmakokinetic behavior, rather than to exceptional affinity to one of the examined binding sites.     

八种新烟碱类杀虫剂对地熊蜂工蜂的毒性及风险评估

【目的】评价新烟碱类杀虫剂对地熊蜂Bombus terrestris工蜂的毒性和生态风险性,为温室施用新烟碱类杀虫剂提供科学依据。【方法】分别采用饲喂法和接触法测定了噻虫嗪、噻虫胺、啶虫脒、吡虫啉、烯啶虫胺、呋虫胺、噻虫啉和氟吡呋喃酮8种新烟碱类杀虫剂对地熊蜂成年工蜂的急性经口和急性接触毒性。同时评估了8种新烟碱类杀虫剂对地熊蜂工蜂的生态风险性。【结果】8种杀虫剂经饲喂法测定,噻虫胺对地熊蜂成年工蜂的毒性最高,24 h和48 h的LD 50值分别为0.0433和0.0330μg a.i./蜂;氟吡呋喃酮毒性最低,24 h和48 h的LD 50值分别为72.4119和67.9079μg a.i./蜂。接触法测定的毒性与饲喂法测得的结果一致,噻虫胺的毒性最高,24 h和48 h的LD 50值分别为0.0220和0.0192μg a.i./蜂;氟吡呋喃酮的毒性最低,24 h和48 h的LD 50值分别为141.7641和130.3062μg a.i./蜂。生态风险评估表明,啶虫脒、噻虫啉和氟吡呋喃酮对地熊蜂成年工蜂的经口毒性和接触毒性均表现为低风险,吡虫啉、烯啶虫胺和呋虫胺的毒性表现为中等风险。噻虫嗪和噻虫胺对地熊蜂成年工蜂的经口毒性表现为中等风险,而接触毒性则表现为高风险。【结论】检测的8种新烟碱类杀虫剂中啶虫脒、噻虫啉与氟吡呋喃酮对地熊蜂成年工蜂的毒性为低毒,而噻虫嗪、噻虫胺、吡虫啉、烯啶虫胺、呋虫胺这5种杀虫剂均为高毒。在设施蔬菜花期使用地熊蜂授粉时,建议禁用这5种中、高风险的新烟碱类杀虫剂,以避免对熊蜂授粉的危害,而另3种低风险药剂可根据田间试验情况合理施用。     

Insecticide,sugar, and diet effects on feeding and mortality in Rhagoletis indifferens (Dipt., Tephritidae)

The effects of spinosad bait and various insecticides, the presence of sugar in insecticides, and diet on feeding responses and mortality in western cherry fruit fly, Rhagoletis indifferens Curran (Dipt., Tephritidae), were determined. Numbers of feeding events on insecticides with sugar were greater than on insecticides alone, but there was only a small effect of diet on feeding responses to insecticides with sugar. Feeding durations on imidacloprid, thiamethoxam and acetamiprid with sugar were shorter than on sugar water and spinosad bait, as the neonicotinoids paralysed flies quickly. Flies that fed on sugar only (nitrogen‐starved) suffered higher mortalities when exposed to spinosad, thiamethoxam and azinphos‐methyl than to imidacloprid, acetamiprid and indoxacarb, and mortality in between these two groups of treatments when exposed to spinosad bait. Mortalities were greater when sugar was added to insecticides, and were higher in nitrogen‐starved than fully‐fed (yeast extract + sugar fed) flies. Flies that fed once on thiamethoxam were killed more quickly than those that fed once on spinosad bait and spinosad. Results suggest that thiamethoxam is comparable to spinosad in its effects on mortality, and that using it with sugar in bait may also have similar results as using spinosad bait or spinosad. One benefit of using thiamethoxam with sugar may be that it kills flies more quickly, before they can oviposit, than spinosad bait, although whether a fly will feed on it may depend on how much sugar or nitrogenous food it has eaten.     

Development of methods to evaluate susceptibility of soybean aphid to imidacloprid and thiamethoxam at lethal and sublethal concentrations

The soybean aphid, Aphis glycines Matsumura (Homoptera: Aphididae), is a recent introduction (2000) from Asia and has become a serious soybean [Glycine max (L.) Merr. (Fabaceae)] pest in North America. Seed treatments using the neonicotinoid insecticides, imidacloprid and thiamethoxam, have been suggested as a method of control, and the use of these insecticides is becoming widespread. As a consequence, there is increased potential to select for resistance to these compounds. In the case of soybean aphids, baseline susceptibility to neonicotinoid insecticides and standardized methods for bioassay are lacking. A bioassay technique that uses excised soybean leaves immersed in an insecticide solution was developed to determine systemic insecticidal activity at lethal and sublethal concentrations. Mortality and population growth inhibition were evaluated after 7 days. Life table parameters were calculated by exposing 1‐day‐old aphids to three concentrations of thiamethoxam. Aphid mortality and nymph production were recorded daily until the entire cohort collapsed. Soybean aphid age‐specific survivorship, fecundity, net reproductive rate, longevity, intrinsic rate of increase, discrete daily growth rate, and life expectancy were all significantly reduced at higher thiamethoxam concentrations. Soybean aphid response to both insecticides was similar, and both compounds were very toxic with LC₅₀s of 31.3 and 16.9 ng ml^?1 and EC₅₀s of 6.3 and 5.4 ng ml^?1 for imidacloprid and thiamethoxam, respectively. These results indicate that the methods developed in this study had negligible impact on the life table estimates measured and can be used to develop a baseline of susceptibility as a benchmark for subsequent resistance monitoring. Given the rapid and widespread adoption of this new insecticide class, vigilant monitoring for changes in susceptibility will be essential to its long‐term sustainability.     

Movement of soil-applied imidacloprid and thiamethoxam into nectar and pollen of squash (Cucurbita pepo)

There has been recent interest in the threat to bees posed by the use of systemic insecticides. One concern is that systemic insecticides may translocate from the soil into pollen and nectar of plants, where they would be ingested by pollinators. This paper reports on the movement of two such systemic neonicotinoid insecticides, imidacloprid and thiamethoxam, into the pollen and nectar of flowers of squash (Cucurbita pepo cultivars "Multipik," "Sunray" and "Bush Delicata") when applied to soil by two methods: (1) sprayed into soil before seeding, or (2) applied through drip irrigation in a single treatment after transplant. All insecticide treatments were within labeled rates for these compounds. Pollen and nectar samples were analyzed using a standard extraction method widely used for pesticides (QuEChERS) and liquid chromatography mass spectrometric analysis. The concentrations found in nectar, 10 ± 3 ppb (mean ± s.d) for imidacloprid and 11 ± 6 ppb for thiamethoxam, are higher than concentrations of neonicotinoid insecticides in nectar of canola and sunflower grown from treated seed, and similar to those found in a recent study of neonicotinoids applied to pumpkins at transplant and through drip irrigation. The concentrations in pollen, 14 ± 8 ppb for imidacloprid and 12 ± 9 ppb for thiamethoxam, are higher than those found for seed treatments in most studies, but at the low end of the range found in the pumpkin study. Our concentrations fall into the range being investigated for sublethal effects on honey bees and bumble bees.     

5种杀虫剂对滇东白背飞虱种群的毒性及其田间药效

【目的】为持续有效防控白背飞虱,研究云南东部白背飞虱种群对常用5种杀虫剂的敏感性及药剂的田间防治效果。【方法】采用室内稻茎浸渍法测定白背飞虱种群对5种杀虫剂的敏感性,同期通过田间小区试验评价5种杀虫剂对白背飞虱种群的防治效果。【结果】与敏感种群比较,噻虫嗪、噻嗪酮、吡虫啉、吡蚜酮和毒死蜱对滇东白背飞虱种群的LC_(50)分别为0.208、0.459、0.608、3.108、1.256 mg·L~(-1),抗性倍数分别为2.2、10.4、5.6、6.5、5.3倍;白背飞虱对噻虫嗪无抗性,对吡虫啉、吡蚜酮和毒死蜱为低水平抗性,对噻嗪酮为中等水平抗性;5种杀虫剂药后1、5和10 d对白背飞虱种群的田间防控效果均有显著差异。除了吡蚜酮外,其他药剂的防效均在80%以上,其中以吡虫啉和噻嗪酮的持续期较长,药后10 d仍在90%以上;噻虫嗪和吡虫啉药后1和5 d的防效达90%以上;吡蚜酮药效在供试药剂中防效最低,在64.88%～77.82%之间。【结论】滇东师宗白背飞虱种群对噻嗪酮为中等水平抗性,对吡虫啉、吡蚜酮和毒死蜱均为低水平抗性,对噻虫嗪无抗性,田间防控效果以吡虫啉和噻嗪酮为最好。建议滇东稻区可以使用吡虫啉和噻嗪酮药剂防控白背飞虱,注意控制吡蚜酮的使用次数与用量。     

Toxicity of four systemic neonicotinoids to adults of Anoplophora glabripennis (Coleoptera: Cerambycidae)

As part of the ongoing evaluation of different systemic insecticides for prophylactic treatment of trees, responses of the beetle Anoplophora glabripennis (Motschulsky) (Coleoptera: Cerambycidae) to different doses of four systemic neonicotinyl insecticides were studied. Adult beetles were provided with twigs or leaves of trees treated with different concentrations of imidacloprid to evaluate the toxicity of the insecticide through ingestion or contact or through both. Adult beetles also were provided with twigs of host plant treated with clothianidin, dinotefuran, and thiamethoxam to establish dose response of the beetle to these insecticides. Levels of individual insecticides in twigs and leaves were determined by using the "parent" method with high-performance liquid chromatography, and these levels were compared with the applied concentrations to determine their relationship. The LC50 values for detected level of each insecticide in twigs was 5.1 ppm at 24 h, 2.9 at 48 h, and 1.9 ppm at 72 h for imidacloprid; 1.1 ppm at 72 h for clothianidin; 2.2 ppm at 72 h for dinotefuran; and 1.0 ppm at 72 h for thiamethoxam. Our results indicate that mortality of adult beetles resulted not only from the ingestion and contact toxicity but also possibly from the antifeedant effect of imidacloprid.     

Effects of spinosad, spinosad bait, and chloronicotinyl insecticides on mortality and control of adult and larval western cherry fruit fly (Diptera: Tephritidae)

Effects of spinosad, spinosad bait, and the chloronicotinyl insecticides imidacloprid and thiacloprid on mortality of the adults and larvae of western cherry fruit fly, Rhagoletis indifferens Curran (Diptera: Tephritidae), were determined in the laboratory and the field. Spinosad and spinosad bait caused higher adult mortality than imidacloprid, which caused higher mortality than thiacloprid. Only spinosad bait prevented oviposition. All materials were more toxic to adults when ingested than when topically applied. Spinosad bait had the greatest residual toxicity on leaves, killing 100% of adults when aged for 14 d in the field. When materials were sprayed on infested cherries, numbers of live larvae in fruit after 8 d were lower in imidacloprid and thiacloprid than in spinosad and spinosad bait treatments, which did not differ from the control, but all materials reduced larval emergence over 30 d. In the field, spinosad and spinosad bait were as effective in suppressing larval infestations as azinphos-methyl and carbaryl, whereas imidacloprid was effective in most cases and thiacloprid was generally less effective than azinphos-methyl and carbaryl. Overall, results in the laboratory and field show that spinosad and chloronicotinyl insecticides differed significantly in their effectiveness against adults and larvae of R. indifferens but that spinosad, spinosad bait, and imidacloprid seem to be acceptable substitutes for organophosphate and carbamate insecticides for controlling this fruit fly.     

Impact of greenhouse whitefly management on strawberry fruit quality

The greenhouse whitefly, Trialeurodes vaporariorum （Westwood）, is an important pest of strawberries in California, USA. The adults and nymphs feed on phloem sap of leaves to remove the photo-assimilates. The objective of this study is to test the impact of whitefly management with insecticides on strawberry fruit quality. Applications of imidacloprid, thiamethoxam, buprofezin and pyriproxyfen decreased the mean adult whitefly numbers by 2.80-, 2.17-, 1.69- and 1.39-fold, respectively, compared to the untreated control, Similarly, the mean numbers of first and second instar whiteflies were reduced 4.36-, 2.20-, 1.90- and 2.02-fold, respectively, while the mean numbers of third and fourth instars were reduced 5.48-, 2.28-, 2.71- and 1.43-fold, respectively, in plants treated with imidacloprid, thiamethoxam, buprofezin and pyriproxyfen. The mean soluble solids content in imidacloprid, thiamethoxam, buprofezin and pyriproxyfen treatments was 1.04-, 1.06-, 1.03- and 1.04-fold greater, respectively, than that in the control. The whitefly reduction enhanced the mean fruit titratable acidity by 4%-6%. Mean glucose levels in imidacloprid and thiamethoxam treatments were significantly higher than in other treatments. However, the whitefly management did not affect the mean fructose levels, lmidacloprid, thiamethoxam and pyriproxyfen treatments boosted the ascorbic acid levels by up to 4%. The impact of whitefly management on strawberry fruit nutrition and antioxidant capacity is discussed.     

A field study investigating the insecticidal efficacy against Diaphorina citri Kuwayama on Kinnow mandarin,Citrus reticulata Blanco trees

Asian citrus psyllid is a most damaging insect pest of citrus. In this field study, the efficacy of seven insecticides (emamectin benzoate, bifenthrin, chlorfenapyr, fipronil, imidacloprid, pyriproxyfen and thiamethoxam) was evaluated against Diaphorina citri Kuwayama in the citrus orchard of Kinnow mandarin, Citrus reticulata Blanco. The insecticides revealed a differential and substantial relative efficacy against D. citri compared to the untreated plants. The insecticidal effect attributed as percent reduction in insect population was more prominent after three days of spray: highest reduction values were recorded with thiamethoxam (50.89%), imidacloprid (44.27%) and bifenthrin (42.94%) after first spray, and thiamethoxam (83.36%), imidacloprid (73.20%) and bifenthrin (72.66%) after second spray. Thus, neonicotinoids (thiamethoxam and imidacloprid) and pyrethroid (bifenthrin) resulted as highly effective against D. citri at three days after both sprays. At seven days, imidacloprid (63.53%) and fipronil (62.47%) presented relatively higher population reduction after first spray, and thiamethoxam (92.66%) and chlorfenapyr (89.59%) after second spray. At 12 days, the insecticidal effect on insect population became significantly at par after each spray except chlorfenapyr that reflected high population reduction (93.17%) only after second spray. It is also obvious from the data that there is need of regular monitoring to suppress the psyllids population below threshold level by timely application of the second insecticidal spray.     

Development of neonicotinoid resistance in the cotton aphid Aphis gossypii (Hemiptera: Aphididae) in Japan

A neonicotinoid-resistant Aphis gossypii Glover population was first detected from cucumber and sweet pepper crops in Miyazaki Prefecture, Japan, in April 2012. In this study, we determined the insecticide susceptibility of five field-collected populations of A. gossypii to seven neonicotinoids. Insecticide susceptibility was determined by performing bioassays and using the seedling-treatment method. Insecticide susceptibility of a susceptible population of A. gossypii, originally collected from a cucumber field in 2008, was also determined. High mortality (96.4–100 %) was observed in the susceptible population for the seven insecticides. In contrast, the mortality rate of the five field-collected populations collected in 2012 was low for five of the seven neonicotinoid insecticides tested: imidacloprid (26.7–65.5 %), dinotefuran (0–27.3 %), clothianidin (20.0–35.7 %), thiamethoxam (7.1–42.3 %), and nitenpyram (6.7–32.1 %). Mortality was 86.2–100 % for acetamiprid and 90.2–100 % for thiacloprid. The resistance ratio in comparison with the susceptible population was the highest for clothianidin (687-fold), lowest for thiacloprid (17-fold), and ranged from 43- to 253-fold for the other five neonicotinoids. Thus, the frequency of insecticide use needs to be reduced and other insecticides need to be employed in order to prevent the development of resistance to these two insecticides in the future.     

褐飞虱和白背飞虱对几类杀虫剂的敏感性

为了科学用药和抗性治理提供理论基础, 采用稻茎浸渍法测定了2008年7月采自浙江省杭州市和宁波市褐飞虱 Nilaparvata lugens (Stål)种群对7种杀虫剂的抗药性及褐飞虱和白背飞虱Sogatella furcifera (Horváth)种群对16种杀虫剂的敏感性。褐飞虱抗药性测定结果表明, 与相对敏感品系相比, 杭州种群和宁波种群对吡虫啉的抗性倍数分别为479.0倍和366.1倍; 对氯噻啉的抗性倍数分别为81.1倍和50.9倍; 对噻虫嗪的抗性倍数分别为10.3倍和9.4倍; 对噻嗪酮和氟虫腈分别产生了5.0~8.6倍和15.8~17.0倍的抗药性; 对烯啶虫胺和啶虫脒的抗性倍数在3倍以下。两种稻飞虱对杀虫剂的敏感性测定结果表明: 噻虫嗪、噻嗪酮、烯啶虫胺和毒死蜱对褐飞虱和白背飞虱种群都具有较高的室内毒力。当田间褐飞虱和白背飞虱混合发生时, 可选用噻虫嗪、噻嗪酮、烯啶虫胺和毒死蜱进行防治, 不宜使用吡虫啉、氯噻啉和氟虫腈防治。     

内共生菌Cardinium对烟粉虱MED隐种耐药性的影响

【目的】次生内共生菌感染可影响烟粉虱Bemisia tabaci对杀虫剂的敏感性。本研究旨在揭示内共生菌Cardinium感染对烟粉虱B. tabaci MED隐种耐药性的影响。【方法】室内测定海南陵水与山东寿光烟粉虱MED隐种种群内遗传背景一致的Cardinium感染与未感染品系对不同浓度新烟碱类杀虫剂噻虫嗪和吡虫啉的耐药性。【结果】各浓度噻虫嗪和吡虫啉处理后,烟粉虱陵水种群感染Cardinium品系死亡率比未感染品系显著降低;100, 150, 175和200 mg/L噻虫嗪以及175和200 mg/L吡虫啉处理后,烟粉虱寿光种群感染Cardinium品系死亡率比未感染品系显著上升。相对于未感染品系,烟粉虱陵水种群感染Cardinium品系对噻虫嗪、吡虫啉的抗性倍数(RR)分别是1.355和1.847,烟粉虱寿光种群感染Cardinium品系的RR分别是0.790和0.847。【结论】内共生菌Cardinium感染能影响烟粉虱MED隐种对噻虫嗪和吡虫啉的耐药性,且这种影响在不同种群间存在差异。研究结果对于揭示烟粉虱MED隐种的种群适应性及扩张机制具有重要参考价值。     

Hydroxylation of thiacloprid by bacterium Stenotrophomonas maltophilia CGMCC1.1788

Chloropyridinyl neonicotinoid insecticides play a major role in crop protection and flea control on cats and dogs. Imidacloprid, thiacloprid and acetamiprid have in common the 6-chloro-3-pyridinylmethyl group but differ in the nitroguanidine or cyanoamidine substituent on an acyclic or cyclic moiety. Our previous study found that Stenotrophomonas maltophilia CGMCC 1.1788 could hydroxylate imidacloprid to 5-hydroxy imidacloprid, and 5-hydroxy imidacloprid was easily converted to 10–19 times higher insecticidal olefin imidacloprid against aphid or whitefly. Acetamiprid could be transformed by S. maltophilia to form N-demethylation product(IM 2-1). In this paper, we examined S. maltophilia CGMCC 1.1788’s ability of transformation of thiacloprid. S. maltophilia CGMCC 1.1788 can hydroxylate thiacloprid to 4-hydroxy thiacloprid characterized by HPLC-MS/MS and NMR analysis, however 4-hydroxy thiacloprid could not be converted to olefin thiacloprid under acid conditions like imidacloprid, whereas oxidized and decyonated simultaneously to form 4-ketone thiacloprid imine in alkaline solution. Bioassays indicated that 4-hydroxy thiacloprid had 156 times lower insecticidal activity than thiacloprid, and the ketone-imine derivative almost had no toxicity towards aphid. Though both imidacloprid and thiacloprid are hydroxylated by S. maltophilia CGMCC 1.1788 at the same carbon atom position, however the structural difference between in imidacloprid and thiacloprid, originate the entire discrepancy in bioefficacy of metabolite and its further degrading pathway. These results explain that why thiacloprid is classified as not relevant grade for soil and seed applications, whereas imidacloprid is recommended and acetamiprid is limited.     

Use of residue profile analysis to identify modes of insecticide activity contributing to control of plum curculio in apples

Residue profile analysis techniques were developed, along with laboratory and field-based bioassays to describe the modes of insecticidal activity responsible for the control of the plum curculio, Conotrachelus nenuphar (Herbst), in apples (Malus spp.). Adult plum curculios were treated in laboratory topical bioassays to determine acute contact activity and lethal time for five insecticides. Azinphosmethyl had the highest levels of toxicity and shortest lethal time values, followed by the neonicotinoids thiacloprid, thiamethoxam, and imidacloprid, whereas indoxacarb had the highest LD50 and LT50 values for topical exposure. Field-based residual activity bioassays assessed adult mortality, and fruit and leaf injury from plum curculio exposed to 4 h, 7 d, and 14 d field-aged residues. All compounds caused significant levels of mortality to plum curculio when adults were exposed to fruit clusters 4 h post-application. Thiacloprid, thiamethoxam, and imidacloprid showed oviposition deterrence, antifeedant, and repellency effects in the 7- and/or 14 d residual bioassays and protected fruit in the absence of significant lethal activity. Indoxacarb maintained lethal activity throughout the study intervals, with the incidence of plum curculio feeding, suggesting that ingestion is an important mode of entry. For the neonicotinoids thiacloprid, thiamethoxam and imidacloprid plum curculio mortality was highly correlated with fruit and leaf surface residues. As surface residues declined, sublethal effects such as oviposition deterrence and antifeedant effect remained. The value of the plant-insect-chemistry triad model for describing the temporal dimensions of insecticidal modes of activity and understanding a compound's critical performance characteristics is discussed.     

Can insecticide mixtures be considered to surmount neonicotinoid resistance in Bemisia tabaci?

Cotton whitefly, Bemisia tabaci is an important polyphagous pest worldwide. It is exposed to various chemical insecticides throughout the year, resulting in the rapid development of insecticide resistance. Mixtures of insecticides with distinct modes of action could enhance the toxicity of chemicals more effectively than sequences or rotations in resistant pest populations. Bioassays were conducted to study the efficacy of mixtures of neonicotinoid and ketoenol insecticides at different ratios against a laboratory susceptible (Lab-WB) and a neonicotinoid resistant (TMX-SEL) strain of B. tabaci Asia I. The results showed that mixtures of imidacloprid, acetamiprid, thiamethoxam or dinotefuran with spiromesifen at 1:1, 1:10 and 1:20 ratios and of imidacloprid, thiamethoxam or dinotefuran with spirotetramat at 1:1 ratio significantly increased (p < 0.05) toxicity to neonicotinoids in TMX-SEL strain. The combination indices of each tested neonicotinoids + ketoenols at 1:1 ratio and of acetamiprid + spiromesifen, and imidacloprid or dinotefuran + spirotetramat at 1:10 ratio for TMX-SEL strain were significantly below 1, suggesting synergistic interactions. The inhibitors PBO and DEF largely overcame resistance to the tested neonicotinoids, while none of the synergists significantly restored the susceptibility of B. tabaci to ketoenols. Increased activities of P450 monooxygenase and esterase were observed in TMX-SEL strain with an elevated 2.76 and 1.32-fold, respectively. Mixtures of neonicotinoids with spiromesifen or spirotetramat at a 1:1 ratio could be used to restore the neonicotinoid susceptibility in B. tabaci.     

Insecticide resistance in Bemisia tabaci from Cyprus

Abstract A comprehensive study on the Bemisia tabaci (biotype B) resistance to neonicotinoid insecticides imidacloprid, acetamiprid and thiamethoxam, and pyrethroid bifenthrin was conducted in Cyprus. The resistance level to eight field‐collected B. tabaci populations was investigated. The activities of enzymes involved in metabolic detoxification and the frequencies of pyrethroid and organophosphates target site resistance mutations were determined. Moderate to high levels of resistance were detected for imidacloprid (resistance factor [RF] 77–392) and thiamethoxam (RF 50–164) while low resistance levels were observed for acetamiprid (RF 7–12). Uniform responses by the Cypriot whiteflies could be observed against all neonicotinoid insecticides. No cross‐resistance between the neonicotinoids was detected as well as no association with the activity of the P450 microsomal oxidases. Only imidacloprid resistance correlated with carboxylesterase activity. Low to extremely high resistance was observed for insecticide bifenthrin (RF 49–1 243) which was associated with the frequency of the resistant allele in the sodium channel gene but not with the activity of the detoxification enzymes. Finally, the F331W mutation in the acetylcholinesterase enzyme ace1 gene was fixed in all B. tabaci populations from Cyprus.     

Variation in susceptibility and selection for resistance to imidacloprid and thiamethoxam in Mediterranean populations of Orius laevigatus

Imidacloprid and thiamethoxam are neonicotinoids that have been tested in several Orius species, including Orius laevigatus (Fieber) (Hemiptera: Anthocoridae), but not the variability in their effect among Orius populations of a single species. In this study, the variation in susceptibility to imidacloprid and thiamethoxam in 30 Mediterranean wild populations and four commercial populations of O. laevigatus was investigated in the laboratory using a standard dip bioassay method. Lethal concentration values (LC₅₀) and the mortality of adults at the maximum field rate (MFR) were calculated. The range of LC₅₀ of thiamethoxam was from 0.7 to 5.9 mg l^?1, an 8.4‐fold variability, obtaining mortality at MFR (100 mg l^?1) of >89.1% in all populations. The baseline obtained a value of 2.1 mg l^?1, which is very low compared to the MFR. For imidacloprid, the LC₅₀ varied from 7.7 to 94.7 mg l^?1 (12.3‐fold variability). Mortalities at the MFR (150 mg l^?1) were 57.7–99.2%, that is, more variable than for thiamethoxam. The LC₅₀ value of the baseline was 48.7 mg l^?1, also low compared to the MFR. This variation was exploited to select two populations resistant to thiamethoxam and imidacloprid, respectively. Artificial selection for on average 40 cycles significantly increased the resistance to thiamethoxam (LC₅₀ = 149.1 mg l^?1) and imidacloprid (LC₅₀ = 309.9 mg l^?1). Mortalities at the MFR in the thiamethoxam‐ and imidacloprid‐resistant populations were 44.5 and 36.9%, respectively. These results demonstrate that resistance can be enhanced in biocontrol agents by artificial selection under laboratory conditions, starting with populations showing no or very low tolerance. Our neonicotinoid‐resistant populations might enhance the wider adoption of biological control by allowing punctual or hotspot applications of neonicotinoids to control several main and secondary pests.