六种新烟碱类杀虫剂残留在苹果实验室模拟加工中的变化

为明确苹果中残留的烯啶虫胺、噻虫嗪、吡虫啉、噻虫胺、呋虫胺和啶虫脒6种新烟碱类药剂在不同加工过程中的变化情况,采用高效液相色谱法研究了6种药剂在苹果实验室罐头、果酱、果酒和果醋模拟加工过程中的残留量变化。结果表明:在苹果罐头加工过程中,6种药剂在罐头中残留量与初始浓度相比均显著降低,其中吡虫啉和噻虫胺在罐头中的加工因子较高,均为0.8,啶虫脒在罐头中的加工因子最低,为0.1。罐头汁中烯啶虫胺的加工因子最高,为0.5,其次为啶虫脒和噻虫嗪,均为0.4。在果酱加工过程中,烯啶虫胺、噻虫嗪、吡虫啉、噻虫胺、呋虫胺和啶虫脒的加工因子分别为0.8、0.9、0.9、1.0、0.9和0.9。在果酒中除吡虫啉的加工因子为0.1外,其余药剂加工因子均小于0.1。在果醋中除噻虫胺有少量残留(0.05 mg/kg)外,其余药剂均低于检出限。6种新烟碱类药剂在苹果实验室模拟加工过程中,加工因子均小于1,残留降低。     

新烟碱类杀虫剂种子包衣防治麦蚜的可行性评价

为评价不同新烟碱类杀虫剂处理种子防治小麦蚜虫的应用潜力,采用种子包衣法分别在室内及田间比较了吡虫啉、噻虫嗪、啶虫脒、烯啶虫胺、噻虫啉防治小麦蚜虫的效果及安全性,并测定了吡虫啉和噻虫嗪的持效、对天敌和小麦产量的影响及其在小麦籽粒中的最终残留量。结果表明,在2.4、3.6和4.8 g/kg种子剂量下,啶虫脒明显降低小麦出苗率,而其它药剂均无显著影响;至抽穗前烯啶虫胺、啶虫脒和噻虫啉对麦蚜的防效低,吡虫啉和噻虫嗪则均有较高防效,在58.17%以上,而在小麦抽穗扬花期防效下降,为33.57%~60.46%。吡虫啉和噻虫嗪对叶部麦蚜防效均相应高于穗部。与喷雾处理相比,吡虫啉、噻虫嗪各剂量种子包衣对瓢虫和蚜茧蜂等天敌昆虫影响小,在3.6、4.8 g/kg种子剂量下,小麦千粒重和产量无显著差异,且在小麦籽粒中的残留量低。表明吡虫啉和噻虫嗪种子包衣防治麦蚜的应用潜力大。     

山东省不同地区棉蚜对新烟碱类杀虫剂的抗药性检测及酶抑制剂的增效作用研究

为明确山东省棉蚜对新烟碱类杀虫剂的抗性水平,采用毛细管微量点滴法测定了泰安、聊城和东营3个田间种群及1个敏感种群对吡虫啉、烯啶虫胺、啶虫脒、噻虫嗪、噻虫啉、噻虫胺6种新烟碱类杀虫剂的敏感性,同时测定了磷酸三苯酯(TPP)、顺丁烯二酸二乙酯(DEM)和增效醚(PBO)3种酶抑制剂的增效作用。结果表明:泰安棉蚜种群对烯啶虫胺的抗性倍数为16.95,处于中等抗性水平,对吡虫啉和啶虫脒的抗性倍数分别为5.69和9.57,已产生低水平抗性,对噻虫胺、噻虫嗪和噻虫啉的抗性倍数均小于3.0,仍较敏感;聊城棉蚜种群对吡虫啉、啶虫脒和噻虫嗪的抗性倍数分别为28.51、25.88和18.16,属中等抗性水平,对噻虫啉和噻虫胺的抗性倍数分别为6.01和6.37,已产生低水平抗性,对烯啶虫胺仍处于敏感阶段;东营棉蚜种群对吡虫啉、啶虫脒和噻虫胺的抗性倍数分别为37.95、21.52和12.95,已产生中等水平抗性,对噻虫啉、烯啶虫胺和噻虫嗪的抗性倍数分别为7.07、6.38和4.75,处于低水平抗性阶段。多功能氧化酶抑制剂PBO和羧酸酯酶抑制剂TPP对6种供试新烟碱类杀虫剂的增效作用明显,谷胱甘肽-S-转移酶抑制剂DEM对这6种药剂也具有一定的增效作用。研究表明,山东省泰安等3地区棉蚜种群对6种新烟碱类杀虫剂均产生了不同程度的抗药性,多功能氧化酶和羧酸酯酶可能在棉蚜对该类杀虫剂的抗性中起主要作用,谷胱甘肽-S-转移酶可能也具有一定的作用。     

30％吡蚜·噻虫胺悬浮剂对水稻稻飞虱的田间防效

为了解杀虫剂在农业生产上的用药安全性,本研究以20％烯啶虫胺水剂和25％吡蚜酮悬浮剂作为对照药剂,调查了30％吡蚜·噻虫胺悬浮剂对稻飞虱的田间防治效果.试验结果表明,30％吡蚜·噻虫胺悬浮剂对水稻安全,对稻飞虱的防治效果高于2种对照药剂,且防治效果随着施药时间的延长而增强.施药后15 d,稻飞虱的虫口减退率达到90.3...     

毒死蜱在梨果实不同部位的残留及消解动态

为探明毒死蜱在梨果实不同部位的残留及消解规律,以20 a生鸭梨（Pyrus bretschneideri Rehd.cv.Yali）为试材,于果实生长期在套袋后向整株喷施48%毒死蜱乳油500倍液（有效成分960 mg/L）,分析毒死蜱向果实中的运输及分配规律;于果实成熟期在采收前向果面喷施48%毒死蜱乳油1 000倍液（有效成分480 mg/L）,分析采后毒死蜱在梨果实不同组织中的分布特征。采用乙腈萃取和GC-NPD检测方法,测定不同处理试材中的毒死蜱含量。结果表明,在果实套袋情况下,整株喷施毒死蜱后72 h内果实不同部位（果心除外）毒死蜱含量均呈现先逐渐上升而后下降趋势,其中果柄、果皮和果梗洼中毒死蜱最高含量值及其出现的时间分别为6.66 mg/kg（12 h）、2.42 mg/kg（24 h）和0.09 mg/kg（12 h）,表明套袋果实毒死蜱来源于枝叶运输,经果柄进入果实后易向果皮累积;而未套袋果施药后24和72 h果皮中毒死蜱含量分别为套袋果的12.56和7.29倍,表明套袋可有效降低果实中毒死蜱的残留量。于果实成熟期向果面喷施毒死蜱后7、14和25 d,果皮中毒死蜱残留量分别为15.54、13.70和12.81 mg/kg,占全果含量的100%,而果肉中毒死蜱残留量低于本检测方法的最低检出浓度（0.05 mg/kg）,因此果皮为果实中毒死蜱主要残留部位,且贮藏期果皮中毒死蜱不易向果肉扩散。     

14种杀虫剂对芹菜蚜的毒力及协同增效研究

本研究旨在明确不同杀虫剂对芹菜蚜的毒力以及杀虫剂复配对芹菜蚜的协同增效作用,从而找出最佳的农药配比,对芹菜蚜进行科学有效地防治.通过浸渍法测定了14种杀虫剂单剂及烯啶虫胺与氟啶虫胺腈复配组合物对芹菜蚜的室内毒力;同时采用玻璃管药膜法测定了吡虫啉、噻虫嗪和高效氯氟氰菊酯对芹菜蚜虫的触杀毒力.结果 表明:供试药剂对芹菜蚜虫...     

叶菜中三种新烟碱类农药的残留吸附动力学和复合效应初探

采用乙腈提取,QuEChERS方法净化,超高压液相色谱仪检测的方法,动态监测3种新烟碱类农药单一及混合使用后青菜中吡虫啉、啶虫脒及噻虫嗪的残留量变化,并进行吸附动力学分析。结果表明,青菜中3种农药的残留量随时间延长增加,不同处理组分别在24~48h达到残留量最高值,之后残留量缓慢降低并趋于稳定。经卡方检验分析,3种农药在青菜中的吸附行为更符合准一级动力学模型,且决定系数R2大部分大于0.9。3种农药混合使用时存在相互作用,相较于农药的单独使用,混用能够提高各自在青菜中的吸附速率。吡虫啉与啶虫脒之间存在相互促进作用,混合使用后各自的残留量和峰值均提高。但两者与噻虫嗪存在抑制作用,混用后青菜中噻虫嗪的最高残留量降低。该研究为农药复合残留风险评估和田间混合施药提供了基础数据。     

基于推荐用量分析我国新烟碱类杀虫剂的登记现状

本文对目前中国农药信息网上公布登记的吡虫啉、烯啶虫胺、啶虫脒、噻虫啉、噻虫嗪、噻虫胺、呋虫胺、氯噻啉、哌虫啶、环氧虫啶等10种新烟碱类杀虫剂的信息进行了查询,分别从登记剂型、作物、防治靶标等方面对这10种杀虫剂的登记推荐有效成分用量情况进行了统计分析,最后,挑选用量范围最大的3种有效成分,5种作物,5种靶标进行组合,并对可能的18种组合进行了数据分析。结果发现:1)在防治草坪-蛴螬和甘蔗-蔗螟上,吡虫啉的有效成分用量要明显高于噻虫嗪和噻虫胺两种药剂,最高分别为2 100.00和1 500.00 g/hm~2;2)在防治韭菜-韭蛆上,噻虫嗪的有效成分用量要明显高于吡虫啉和噻虫胺,最高为1 732.50 g/hm~2;3)在防治小麦-蚜虫方面,吡虫啉的推荐有效成分用量范围最大(相差120倍),且偏高数值点最多;4)在防治水稻-飞虱上,同样是吡虫啉的偏高数值点最多。为减少农药施用,建议在病虫防治时推荐应用有效成分用量较低的农药类型(包括推荐有效成分用量更低的农药剂型和生物活性更高的农药有效成分)。未来农药登记用量将在农药最低有效剂量研究的基础上,针对不同药剂在不同作物的特定防治靶标提出更加科学、合理的推荐用量,为我国农药的合理减施提供科学依据。     

20种杀虫剂对草地贪夜蛾的杀卵活性

在前期测定14种杀虫剂对草地贪夜蛾杀卵活性的基础上,本文采用浸渍法又测定了20种不同类型杀虫剂的杀卵活性,以期为草地贪夜蛾卵期防治药剂的选择提供更全面的参考。结果表明,所测的20种杀虫剂均具有一定的杀卵活性。在100 mg/L浓度下,溴氰菊酯、高效氯氰菊酯和乙基多杀菌素表现出出色的杀卵活性,能够完全抑制卵的孵化,杀虫双的杀卵活性最差,低于10%。而噻虫胺、氯虫苯甲酰胺、高效氯氟氰菊酯、多杀霉素、联苯菊酯、噻虫啉、氧乐果、噻虫嗪、甲氰菊酯、烯啶虫胺和啶虫脒的杀卵活性相对较好,其校正死亡率在70.95%～98.52%之间,毒死蜱、吡虫啉、辛硫磷、虫螨腈和杀虫单的杀卵活性相对较差,在42.26%～61.51%之间。在10 mg/L浓度下,噻虫胺、乙基多杀菌素和噻虫啉的杀卵活性均在70%以上,而杀虫双、毒死蜱和烯啶虫胺的杀卵活性低于15%。特别是在100 mg/L和10 mg/L浓度下,新烟碱类杀虫剂噻虫胺和噻虫啉对草地贪夜蛾表现出较高的杀卵活性,分别为98.52%、76.91%和89.37%、72.44%。上述药剂在田间对草地贪夜蛾的杀卵效果还有待进一步验证。     

噻虫胺种子处理对西瓜生长发育的影响及其残留分析

为明确新烟碱类杀虫剂噻虫胺种子处理对西瓜生长发育和品质的影响, 以及在西瓜中的残留状况, 本研究以10%噻虫胺种子处理悬浮剂为供试药剂, 采用拌种试验, 开展噻虫胺对西瓜生长发育的影响及残留分析研究。结果表明, 噻虫胺有效成分用量100~250 g/100 kg范围内, 对西瓜出苗安全; 噻虫胺拌种处理对西瓜苗期的株高、茎粗、叶绿素含量和叶面积有一定的促进作用, 随着西瓜的生长促进作用减弱, 西瓜出苗后30 d, 各处理间差异不显著; 噻虫胺各处理西瓜产量均高于空白对照, 对西瓜有一定的增产作用; 噻虫胺拌种可不同程度地提高西瓜果实中可溶性糖、可溶性固形物含量, 提升西瓜的品质; 随着西瓜生长发育, 叶片内噻虫胺含量逐渐降低, 出苗后45 d, 叶片内未检测到噻虫胺残留; 西瓜收获时果实中未检测到噻虫胺残留, 西瓜根部土壤中噻虫胺的残留量在0.041 2~0.097 5 mg/kg之间。综上所述, 噻虫胺100~250 g/100 kg用量范围内处理西瓜种子, 对西瓜苗期生长有一定促进作用, 并可提高产量, 改善西瓜的品质, 叶片内噻虫胺含量随植株生长逐渐降低, 果实中无残留, 本研究为噻虫胺种子处理在西瓜生产实践中合理、安全、高效的应用提供技术支撑。     

八种杀虫剂对黑粪蚊的防治效果及残留分析

选择8种杀虫剂,分别在实验室和菇房条件下研究其对黑粪蚊的防治效果和对平菇菌丝生长的影响,并分析施药后不同时间平菇中的农药残留.结果表明,40%辛硫磷EC、40%氧乐果EC、48%毒死蜱EC对黑粪蚊具有很好的防治效果,但对平菇菌丝的抑制率明显高于其它药剂;10%吡虫啉WP、4.5%高效氯氰菊酯EC不仅对黑粪蚊成、幼虫具有良好的防治效果,而且使用后对平菇菌丝生长的影响较小;2.5%高效氯氟氰菊酯EW、4.5%高效氯氰菊酯EC、1.8%阿维菌素EC等使用5天后均未检测到农药残留,5%氟虫腈SC和10%吡虫啉WP药后15天仍能检测到残留.     

苯醚甲环唑在套袋与不套袋苹果中的残留及消解动态

通过两年田间试验并结合气相色谱-电子捕获检测(GC-ECD)技术,研究比较了苹果套袋 和不套袋2种不同栽培方式下苯醚甲环唑在苹果中的残留及消解动态。结果表明:2011和2012年, 苯醚甲环唑在未套袋苹果中的原始沉积量分别为0.44和0.17 mg/kg,消解半衰期分别为12.8和15.5 d;2012年其在套袋苹果中的原始沉积量为0.056 mg/kg,半衰期为31.9 d。两年的试验表明,于苹果收获前35~42 d,按照10%苯醚甲环唑水分散粒剂的推荐剂量和1.5倍推荐剂量(有效成分分别为66.7和100 mg/L)施药2次和3次, 距末次施药后7 d采收,套袋和不套袋果实中苯醚甲环唑的残留量均低于我国最大残留限量(MRL)值0.5 mg/kg,其中套袋处理均低于0.03 mg/kg,表明苯醚甲环唑按照推荐剂量及次数施用是安全的;在套袋方式下,苯醚甲环唑残留量明显降低。     

Toxicities and sublethal effects of seven neonicotinoid insecticides on survival, growth and reproduction of imidacloprid-resistant cotton aphid, Aphis gossypii

BACKGROUND: Imidacloprid has been a major neonicotinoid insecticide for controlling Aphis gossypii (Glover) (Homoptera: Aphididae) and other piercing–sucking pests. However, the resistance to imidacloprid has been recorded in many target insects. At the same time, cross‐resistance of imidacloprid and other insecticides, especially neonicotinoid insecticides, has been detected. RESULTS: Results showed that the level of cross‐resistance was different between imidacloprid and tested neonicotinoid insecticides (no cross‐resistance: dinotefuran, thiamethoxam and clothianidin; a 3.68–5.79‐fold cross‐resistance: acetamiprid, nitenpyram and thiacloprid). In the study of sublethal effects, imidacloprid at LC₂₀ doses could suppress weight gain and honeydew excretion, but showed no significant effects on longevity and fecundity of the imidacloprid‐resistant cotton aphid, A. gossypii. However, other neonicotinoid insecticides showed significant adverse effects on biological characteristics (body weight, honeydew excretion, longevity and fecundity) in the order of dinotefuran > thiamethoxam and clothianidin > nitenpyram > thiacloprid and acetamiprid. CONCLUSION: The results indicated that dinotefuran is the most effective insecticide for use against imidacloprid‐resistant A. gossypii. To avoid further resistance development, the use of nitenpyram, acetamiprid and thiacloprid should be avoided on imidacloprid‐resistant populations of A. gossypii. Copyright © 2011 Society of Chemical Industry     

Effects of mutations in Drosophila nicotinic acetylcholine receptor subunits on sensitivity to insecticides targeting nicotinic acetylcholine receptors

Several strains of Drosophila melanogaster possess mutant alleles in nicotinic acetylcholine receptor (nAChR) subunits, Dα1 and Dβ2 that confer resistance to neonicotinoids such as imidacloprid and nitenpyram, and Dα6, that confers resistance to spinosyns. These mutant strains were bioassayed with a selected set of nAChR active insecticides including neonicotinoids, spinosad, and sulfoxaflor, a new sulfoximine insecticide. All of the neonicotinoids examined, except dinotefuran showed reduced insecticidal efficacy on larvae of the Dα1 mutant, suggesting that this subunit may be important in the action of these insecticides. All of the neonicotinoids, including dinotefuran, showed reduced insecticidal efficacy on larvae possessing the Dβ2 mutation. A similar pattern of broad neonicotinoid resistance to that of Dβ2 alone was also observed for larvae with both the mutations (Dα1 + Dβ2). The Dβ2 mutation exhibited a lower level of cross-resistance to sulfoxaflor (<3-fold) than to any of the neonicotinoids (>13-fold). In contrast, there was no cross-resistance for any of the neonicotinoids or sulfoxaflor in adult flies with the Dα6 mutation, which confers high levels of resistance to spinosad. Thus in the D. melanogaster strains studied, target site resistance observed for the neonicotinoids and the spinosyns does not translate directly to resistance towards sulfoxaflor.     

Susceptibility to neonicotinoids and risk of resistance development in the brown planthopper, Nilaparvata lugens (Stål) (Homoptera: Delphacidae)

BACKGROUND: In recent years, outbreaks of the brown planthopper, Nilaparvata lugens (Stål), have occurred more frequently in China. The objective of this study was to determine the susceptibility of N. lugens to neonicotinoids and other insecticides in major rice production areas in China. RESULTS: Results indicated that substantial variations in the susceptibility to different insecticides existed in N. lugens. Field populations had developed variable resistance levels to neonicotinoids, with a high resistance level to imidacloprid (RR: 135.3–301.3‐fold), a medium resistance level to imidaclothiz (RR: 35–41.2‐fold), a low resistance level to thiamethoxam (up to 9.9‐fold) and no resistance to dinotefuran, nitenpyram and thiacloprid (RR < 3‐fold). Further examinations indicated that a field population had developed medium resistance level to fipronil (up to 10.5‐fold), and some field populations had evolved a low resistance level to buprofezin. In addition, N. lugens had been able to develop 1424‐fold resistance to imidacloprid in the laboratory after the insect was selected with imidacloprid for 26 generations. CONCLUSION: Long‐term use of imidacloprid in a wide range of rice‐growing areas might be associated with high levels of resistance in N. lugens. Therefore, insecticide resistance management strategies must be developed to prevent further increase in resistance. Copyright © 2008 Society of Chemical Industry     

Resistance and cross-resistance to neonicotinoid insecticides and spinosad in the Colorado potato beetle, Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae)

The Colorado potato beetle, Leptinotarsa decemlineata (Say), has developed resistance to many insecticides used for its control, recently including imidacloprid, a neonicotinoid compound. Other neonicotinoids are now being deployed to control this pest. A key point in the strategies of resistance management is the monitoring of resistance and cross-resistance. In the summer of 2003, imidacloprid-resistant adult Colorado potato beetles collected from Long Island, New York, USA were bioassayed using topical applications of imidacloprid and nine other neonicotinoids. Compared to a standard susceptible strain, the Long Island beetles showed 309-fold resistance to imidacloprid, and lower levels of cross-resistance to all other neonicotinoids, despite these never having been used in the field, i.e., 59-fold to dinotefuran, 33-fold to clothianidin, 29-fold to acetamiprid, 28-fold to N-methylimidacloprid, 25-fold to thiacloprid, 15-fold to thiamethoxam, 10-fold to nitenpyram, but less than 2-fold to nicotine. In injection bioassays, high resistance to imidacloprid was also found (116-fold). Piperonyl butoxide partially suppressed resistance to imidacloprid, but the resistance level was still over 100-fold, indicating that other mechanisms were primarily responsible for resistance. Low levels of resistance (8- to 10-fold) were found to the nicotinic activator, spinosad, in an imidacloprid-resistant strain collected from the same field in 2004. The cross-resistance seen with all the neonicotinoids tested suggests that the rotation of imidacloprid with other neonicotinoids may not be an effective long-term resistance management strategy. Rotation with spinosad also carries some risk, but it is unlikely that spinosad resistance in this case is mechanistically related to that for the neonicotinoids.     

Comparative analysis of neonicotinoid binding to insect membranes: I. A structure-activity study of the mode of [3H]imidacloprid displacement in Myzus persicae and Aphis craccivora

Neonicotinoids bind selectively to insect nicotinic acetylcholine receptors with nanomolar affinity to act as potent insecticides. While the members of the neonicotinoid class have many structural features in common, it is not known whether they also share the same mode of binding to the target receptor. Previous competition studies with [3H]imidacloprid, the first commercialised neonicotinoid, indicated that thiamethoxam, representing a novel structural sub-class, may bind in a different way from that of other neonicotinoids. In the present work we analysed the mode of [3H]imidacloprid displacement by established neonicotinoids and newly synthesized analogues in the aphids Myzus persicae Sulzer and Aphis craccivora Koch. We found two classes of neonicotinoids with distinct modes of interference with [3H]imidacloprid, described as direct competitive inhibition and non-competitive inhibition, respectively. Competitive neonicotinoids were acetamiprid, nitenpyram, thiacloprid, clothianidin and nithiazine, whereas thiamethoxam and the N-methyl analogues of imidacloprid and clothianidin showed non-competitive inhibition. The chloropyridine or chlorothiazole heterocycles, the polar pharmacophore parts, such as nitroimino, cyanoimino and nitromethylene, and the cyclic or acyclic structure of the pharmacophore were not relevant for the mode of inhibition. Consensus structural features of the neonicotinoids were defined for the two mechanisms of interaction with [3H]imidacloprid binding. Furthermore, two sub-classes of non-competitive inhibitors can be discriminated on the basis of their Hill coefficients for imidacloprid displacement. We conclude from the present data that the direct competitors share the binding site with imidacloprid, whereas non-competitive compounds, like thiamethoxam, bind to a different site or in a different mode.     

Variation in response to neonicotinoid insecticides in peach-potato aphids,Myzus persicae (Hemiptera: Aphididae)

Laboratory bioassays applying the neonicotinoid insecticides imidacloprid, acetamiprid and nitenpyram against clones of the peach-potato aphid Myzus persicae (Sulzer) demonstrated that these compounds effectively circumvent the known carboxylesterase, modified acetylcholinesterase (MACE) and knock-down (kdr) insecticide resistance mechanisms in this species. However, some clones showed cross-tolerance (up to 18-fold) of these compounds relative to susceptible standards. A survey assessing the frequency of neonicotinoid tolerance in M persicae in the UK, based on samples collected from the field and glasshouses between 1997 and 2000, showed that such tolerance is still rare. Experiments on neonicotinoid-susceptible and -tolerant populations of M persicae under simulated field conditions in the laboratory showed that, although the latter were well controlled by imidacloprid applied at recommended application rates, they were more likely to survive and reproduce when this compound was applied at lower concentrations. Such conditions are probably periodically present in imidacloprid-treated field and glasshouse crops. Selection favouring tolerant forms of M persicae could lead to increases in their frequency and the evolution of more potent resistance to neonicotinoids.