分散固相萃取-气相色谱法测定茶鲜叶中7种拟除虫菊酯类农药残留

建立了超声波提取、分散固相萃取净化、气相色谱-电子捕获法(GC-ECD)同时测定茶鲜叶中甲氰菊酯、高效氯氟氰菊酯、氯菊酯、氟氯氰菊酯、氯氰菊酯、氰戊菊酯和溴氰菊酯7种拟除虫菊酯类农药残留的方法。样品采用V(乙酸)∶V(乙腈)=1∶99的混合溶剂超声提取,适量乙二胺-N-丙基硅烷(PSA)、十八烷基硅烷键合硅胶(C18)和石墨化碳黑(GCB)吸附剂净化,GC-ECD测定,基质外标法定量。结果表明:在0.004~2 mg/L范围内,7种拟除虫菊酯类农药的峰面积与相应质量浓度间呈良好的线性关系,相关系数均大于0.999;在0.01~0.5 mg/kg的添加水平下,平均回收率为80%~101%,日内相对标准偏差(RSD)均小于8.4%(n=6),日间RSD均小于9.3%(n=3);7种农药在茶鲜叶中的检出限为0.002~0.02 mg/kg,定量限为0.01~0.05 mg/kg。该方法操作简单、定量准确、溶剂用量少,对检测条件要求低,可同时测定茶鲜叶中7种拟除虫菊酯农药的残留量。     

Genetic basis of resistance and studies on cross-resistance in a population of diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae)

The genetic basis of abamectin resistance was studied in a strain of the diamondback moth, Plutella xylostella (L), following laboratory selection of a field population collected at Xuanhua, Hebei Province, China. Data from the testing of F1 progeny from reciprocal crosses between abamectin-resistant and abamectin-susceptible strains indicated that resistance might be autosomal and incompletely recessive with a degree of dominance of -0.13. Chi-squared analyses from the response of a backcross of crossed F1 progeny and the resistant strain and F2 progeny were highly significant, suggesting that the resistance was probably controlled by more than one gene. The results of cross-resistance studies showed that there was little cross-resistance between abamectin and four pyrethroid insecticides (deltamethrin, beta-cypermethrin, fenvalerate and bifenthrin) and no cross-resistance between abamectin and the acylureas chlorfluazuron or flufenoxuron.     

关于农药乳油制剂的酸碱性技术指标

我国农药制乳油剂酸碱性技术指标以往多用酸度表示，高效氯氰菊酯，溴氰菊酯，氯氟氰菊酯等乳油不同酸度或ｐＨ值的制试样热贮试验表明，对介质酸碱性较敏感的有效成分乳油制剂，质量控制应采用严格的ｐＨ值范围作为技术指标。     

The pyrethrins and related compounds part XXXIX— structure-activity relationships of pyrethroidal esters with cyclic side chains in the alcohol component against resistant strains of housefly (Musca domestica)

Activities of a range of pyrethroidal esters, incorporating structural variations in all regions of the acid and alcohol components, have been measured against two fully characterised and homozygous resistant strains of Musca domestica L. (kdr and super-kdr). The results, limited in this paper to esters of alcohols with cyclic side chains, indicate uniform resistance to the kdr strain across the whole range of structural variations. Against the super-kdr strain, while variation in the acid component has little effect, the resistance factor is sensitive to the nature of the alcohol component, in particular on whether it contains an α-cyano substituent.     

小菜蛾幼虫对拟除虫菊酯类杀虫剂的抗药性与多功能氧化酶的关系

作者就上海梅陇、广州天河和江西莲塘的小菜蛾对拟除虫菊酯的抗药性及其与微粒体多功能氧化酶(MFO)的关系进行了研究。结果表明,上海种群(R)对溴氰菊酯、氰戊菊酯和氯菊酯的 LD_(50)分别是江西种群(S)的>10414倍、2102倍和245倍。广州种群分别为>10414倍、>3569倍和1533倍。活体增效试验表明,酯酶抑制剂 TBPT 在低剂量(0.208μg/虫)时,对溴氰菊酯和氯菊酯都无增效作用,在高剂量(2.08μg/虫)时分别增效41.7倍和110倍。用 MFO的抑制剂 PB 作同样处理时,低剂量的 PB 对溴氰菊酯和氯菊酯的增效作用分别为5倍和12.9倍;高剂量的 PB 对溴氰菊酯增效562倍以上。~(14)C-氰戊菊酯代谢的离体研究结果表明,R 小菜蛾代谢~(14)C-氰戊菊酯的速度是 S 小菜蛾的2.1倍,TBPT 抑制~(14)C-杀灭菊酯的代谢约20%,而PB 抑制50%以上。由此可以得出结论,MFO 是小菜蛾对拟除虫菊酯的主要机理之一。     

Field and laboratory experiments on the response and development of resistance to pesticides and population density ofTetranychus cinnabarinus in ISRAEL

Dosage mortality data for 12 pesticides were determined with females of an insecticide-susceptible strain of the carmine spider mite,Tetranychus cinnabarinus (Boisd.), by the slide dip method; for four of the pesticides which are specific acaricides, also the Munger cell method was used. The LC₅₀s ranged from 0.00078% to 0.041%, with the synthetic pyrethroids being more toxic than the specific acaricides. There were no differences in results between the two assay methods. Four synthetic pyrethroids that were very active againstT. cinnabarinus in laboratory tests were examined in an unsprayed apple orchard for their effect on the population density of spider mites. An upsurge of tetranychid mites was noted 4 weeks after a single application     

拟除虫菊酯类农药对哺乳动物神经毒理的研究进展

对拟除虫菊酯类(SPs)农药对哺乳动物的神经毒理学研究过程及其最新进展进行了综述。拟除虫菊酯类农药是目前使用广泛的一类神经毒性杀虫剂,主要用于农业和卫生害虫的防治。已有研究结果显示拟除虫菊酯类农药对非靶标野生动物和人类的神经系统有一定的毒性作用,其对哺乳动物的神经毒性主要表现为急性和慢性神经毒性,而且其毒性作用与拟除虫菊酯类农药的立体结构相关,有一定的对映体选择性差异。     

Monooxygenase mediated pyrethroid detoxification in sea lice (Lepeophtheirus salmonis)

The role of monooxygenases in detoxification of the pyrethroids cypermethrin and deltamethrin was examined. Four strains of sea lice (Lepeophtheirus salmonis Krøyer) with normal or moderately reduced sensitivity towards the pyrethroids were tested in bioassays by exposure to the pyrethroid alone and in combination with an oxygenase inhibitor, piperonyl butoxide (PBO). The normal (baseline) sensitivity was considered as the sensitivity range for the two most sensitive strains. Pre‐treatment with PBO elevated the sensitivity (P < 0.01) compared with groups exposed to the pyrethroid only. A positive, but not statistically significant, correlation between the activity of haem peroxidases and the pyrethroid concentration immobilizing 50% of the parasites was demonstrated (ρ = 0.500 for deltamethrin and ρ = 0.310 for cypermethrin). The results indicate that cytochrome P450 monooxygenases are involved in detoxification of pyrethroids in sea lice. ¹⁴C‐Deltamethrin was absorbed in a lesser amount in a group of sea lice exposed to a mixture of the compound and PBO than in a group exposed to ¹⁴C‐deltamethrin alone. A significant difference could be demonstrated both immediately after exposure (P < 0.01) and 24 h after exposure (P < 0.05). No significant differences were found between groups pre‐treated with PBO and groups exposed to ¹⁴C‐deltamethrin only. ¹⁴C‐Deltamethrin was taken up mainly through the cuticle, especially the cuticle on the extremities of the ventral surface, and subsequently distributed throughout the body of the parasite. Copyright © 2005 Society of Chemical Industry     

Can selective peptides be combined efficiently with agrochemicals? A new approach to insect control

Sodium channels have been a major target for the development of insecticides such as synthetic pyrethroids. However, insecticides currently available induce resistance and present limited selectivity to insect pests. Molecular and biochemical studies, as well as binding experiments using radiolabelled neurotoxins, have shown that sodium channels expressed in various insect orders must be structurally and pharmacologically different. At least three groups of peptide neurotoxins derived from scorpion venom are highly active on insects and very weakly or practically inactive on mammals. It is proposed that various insecticides are examined for possible cooperative interactions with the peptide toxins highly active on insects, and pairs of ligands are identified that will increase the selectivity not only between mammals and insects but also between different pest and non-pest insects. This is feasible on the basis of the differential allosteric modulations observed between LqhαIT, an α-toxin highly active on insects, and brevetoxin on locust versus cockroach and rat brain sodium channels. Moreover, combination of LqhαIT with the pyrethroid deltamethrin increased the binding of [¹²⁵I] LqhαIT by more than 1.8-fold, and the combined presence of brevetoxin further increased the binding. Such allosteric modulation may provide a new approach to increase the selective activity of pesticides on target organisms by simultaneous application of allosterically interacting drugs, designed on the basis of the selective peptide toxins.     

An Umpolung approach to fluorinated non-ester pyrethroids

The synthesis of novel, fluorinated non-ester pyrethroids by electrophilic fluorination of a stabilised anion with N-fluorobenzenesulfonimide is reported. © 1999 Society of Chemical Industry