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1.
Three insect growth regulators (IGR), the chitin synthesis inhibitors (CSI) teflubenzuron and hexaflumuron and the juvenile hormone mimic (JHM) pyriproxyfen, as well as the organophosphate (OP) pirimiphos-methyl, were evaluated for their activity against the cowpea weevil, Callosobruchus maculatus (F), in cowpea seeds stored for up to 8 months post-treatment. The initial activity data showed that, based on LC50 level, teflubenzuron had strong ovicidal activity (LC50 = 0.056 mg kg(-1)) followed by pirimiphos-methyl (1.82 mg kg(-1)) and pyriproxyfen (91.9 mg kg(-1)). The residual activity data showed that none of the IGRs tested had strong activity when applied at 200 mg kg(-1) in reducing the oviposition rates of C maculatus at various storage intervals up to 8 months post-treatment. However, teflubenzuron reduced adult emergence (F1 progeny), achieving control ranging from 96.2% at 1 month to 94.3% at 8 months. Hexaflumuron showed a similar trend in its residual activity, ranging between 93.8% control at 1 month to 88.2% control at 8 months post-treatment. However, pyriproxyfen was more active than the CSIs tested and caused complete suppression (100% control) of adult emergence at all storage intervals. Unlike the IGRs tested, pirimiphos-methyl applied at 25 mg kg(-1) was more effective in reducing oviposition rates of C maculatus up to 8 months post-treatment. A strong reduction of adult emergence was also observed at various bimonthly intervals (98.6% control at 1 month to 91.6% control at 8 months post-treatment). The persistence of hexaflumuron and pirimiphos-methyl in cowpea seeds was also studied over a period of 8 months. The loss of hexaflumuron residue in treated cowpeas (200 mg kg(-1)) was very slow during the first month post-treatment (4.43%). At the end of 8 months, the residue level had declined significantly to 46.4% of the initial applied rate. The loss of pirimiphos-methyl residue in treated cowpeas (25 mg kg(-1)) was relatively high during the first month post-treatment (36.7%) and increased to 81.6% after 8 months.  相似文献   

2.
Dose-mortality curves were established for 12 insecticides administered by topical application to diapausing larvae from a susceptible codling moth strain. Toxicity varied greatly among the insecticides tested. LC50 values ranged from 0.1 mg kg(-1) for fenoxycarb to over 2800 mg kg(-1) for diflubenzuron and indoxacarb. Discriminating dose levels were determined from dose-mortality reference curves for the detection of resistance in field-collected diapausing larvae.  相似文献   

3.
Crude toxins [toxin(V3450) and toxin(Vp28,) extracted from Lecanicillium (Verticillium) lecanii (Zimmermann) Gams & Zare strain V3450 and Vp28 respectively] were tested for contact toxicity, feeding deterrence and repellent activity against the sweet potato whitefly, Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae). Both toxins showed ovicidal activity to eggs, with LC(50) values of 447 and 629 mg L(-1) respectively. Nymphs of B. tabaci were the most susceptible stages (LC(50) values were calculated at 111 mg L(-1) for toxin(V3450) and 216 mg L(-1) for toxin(Vp28)), and adults were the second most susceptible stages (48 h LC(50) values were calculated at 178 mg L(-1) for toxin(V3450) and 438 mg L(-1) for toxin(Vp28)). Applied to seedlings at a concentration of 400 mg L(-1), the toxins significantly (P < 0.001) reduced the hatching of whitefly eggs and the subsequent survival rate of the nymphs, and the emergence and fecundity of the progeny adults. Both toxins exhibited repellent activity at low concentration (100 mg L(-1)), with repellency index (RI) values of 0.645 for toxin(V3450) and 0.642 for toxin(Vp28), and antifeedant activity at high concentration (1000 mg L(-1)) to adults, with antifeedant index (AFI) values of 0.713 for toxin(V3450) and 0.749 for toxin(Vp28). The results of the present study demonstrate the toxicity, repellence and antifeedant properties of the fungi metabolite toxins on B. tabaci, which might develop as environmentally friendly plant protectant(s).  相似文献   

4.
20种杀虫剂对草地贪夜蛾的杀卵活性   总被引:2,自引:0,他引:2  
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。  相似文献   

5.
BACKGROUND: Imidacloprid is an effective, systemic insecticide for the control of wood-boring insect pests in trees. Systemic applications to trees are often made by soil injections or drenches, and the resulting imidacloprid concentrations in soil or litter may pose a risk of harm to natural decomposer organisms. The authors tested effects of imidacloprid on survival and weight gain or loss of the earthworms Eisenia fetida (Savigny) and Dendrobaena octaedra (Savigny), on leaf consumption rates and cocoon production by D. octaedra and on microbial decomposition activity in laboratory microcosms containing natural forest litter. RESULTS: Dendrobaena octaedra was the most sensitive of the two earthworm species, with an LC(50) of 5.7 mg kg(-1), an LC(10) of about 2 mg kg(-1) and significant weight losses among survivors at 3 mg kg(-1). Weight losses resulted from a physiological effect rather than from feeding inhibition. There were no effects on cocoon production among survivors at 3 mg kg(-1). The LC(50) for E. fetida was 25 mg kg(-1), with significant weight losses at 14 mg kg(-1). There were no significant effects on microbial decomposition of leaf material at the maximum test concentration of 1400 mg kg(-1).CONCLUSION: The results indicate that, when imidacloprid is applied as a systemic insecticide to the soil around trees, it is likely to cause adverse effects on litter-dwelling earthworms if concentrations in the litter reach or exceed about 3 mg kg(-1).  相似文献   

6.
3种新型杀虫剂对苹果黄蚜的毒力效果评价   总被引:1,自引:0,他引:1  
采用浸叶法在室内测定了3种药剂对苹果黄蚜的毒力,并在田间进行了防治试验。室内毒力测定结果表明:供试3种新型药剂中,双丙环虫酯和氟吡呋喃酮对苹果黄蚜的毒力较高,LC50分别为3.16 mg/L和23.58 mg/L,三氟苯嘧啶毒力较低,LC50为329.92 mg/L。田间试验结果表明:3种药剂对苹果黄蚜均有较好的速效性和持效性。17%氟吡呋喃酮可溶液剂和10%三氟苯嘧啶悬浮剂各处理3~7 d防效为82.19%~93.45%,药后30 d防效达到78.91%~87.92%;50 g/L双丙环虫酯可分散液剂2.5 mg/kg和4.2 mg/kg处理药后3~7 d防效为94.64%~97.04%,药后21 d防效仍可达88%以上。因此,3种新型药剂均可以用于防治苹果黄蚜,田间使用时推荐有效成分用量为双丙环虫酯2.5~4.2 mg/kg,氟吡呋喃酮113~170 mg/kg,三氟苯嘧啶28~80 mg/kg。  相似文献   

7.
The effect of the non-steroidal ecdysone agonist methoxyfenozide was evaluated against different developmental stages of the grape berry moth, Lobesia botrana Dennis & Schiffermuller (Lep, Tortricidae). Methoxyfenozide administered orally reduced the fecundity and fertility of adults treated with 1, 5 and 10 mg litre(-1); longevity was not affected. An LC(50) value of 4.5 mg litre(-1) was obtained when applied to eggs of less than 1 day old. Surface treatment was more effective than when applied by spraying. Administered into the diet, methoxyfenozide had a larvicidal effect; older larvae were more susceptible than younger larvae, with LC(50) values of 0.1 mg litre(-1) for L(1), 0.04 for L(3) and 0.02 for L(5). Larvae treated with sub-lethal doses throughout their lives did not emerge as adults at the highest doses (0.08, 0.04, 0.02 and 0.01 mg litre(-1)), with 65% and 40% emergence occurring for the lowest (0.005 and 0.0025 mg litre(-1)). Mortality occurred only in the larval stage.  相似文献   

8.
用叶片药膜法测定了4种常用杀虫剂氧乐果、辛硫磷、三唑磷、吡虫啉对呼和浩特市郊蔬菜基地温室黄瓜上发生的瓜蚜的毒力。结果表明,瓜蚜对吡虫啉最敏感,LC50 仅为4.203 mg/L,氧乐果、辛硫磷、三唑磷对瓜蚜的LC50分别为21.70、38.86、43.30 mg/L。研究明确了3种有机磷杀虫剂对瓜蚜体内乙酰胆碱酯酶AChE均有明显的抑制作用,并随着抑制时间的延长,抑制率增加。I50值分别为氧乐果9.6×10-6mol/L,辛硫磷11.4×10-6mol/L,三唑磷17.1×10-6mol/L。  相似文献   

9.
Two experimental insecticides, AC 303,630 and MK 244, were tested against a laboratory colony and three field strains of Pseudoplusia includens (Walker). Topical application bioassays indicated that permethrin resistance in the field strains ranged from 3.9 to 489.0-fold. In leaf dip bioassays, LC50 and LC90 values for AC 303,630 ranged from 6.7 to 15.1 mg litre ?1 and 8.7 to 28.2 mg litre ?1, respectively, for third-instar larvae. The Louisiana 1991 field strain was significantly more susceptible to AC 303,630 than the laboratory and other field strains. The LC50 (but not LC90) for the Louisiana 1992 field strain was significantly higher than that of the laboratory strain. However, there was no difference in toxicity of AC 303,630 between the field strain with the highest level of permethrin resistance and the laboratory strain. LC50 and LC90 values for MK 244 in leaf dip bioassays ranged from 0.014 to 0.023 mg litre ?1 and 0.079 to 0.174 mg litre ?1, respectively. There were no significant differences in LC 50 or LC 90 among any of the strains for MK 244. Field trials in soybean were also conducted in 1991 and 1992 in an area of Louisiana where permethrin efficacy against P. includens has declined. In both years, AC 303,630 at 0.11–0.22 kg ha ?1, and MK 244 at 0.0042–0.0084 kg ha ?1, provided significantly better control than permethrin at 0.11 kg ha ?1, and control equal to the recommended standard, thiodicarb. These studies indicate no cross-resistance exists between the experimental insecticides and permethrin.  相似文献   

10.
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).  相似文献   

11.
5种药剂对枸杞棉蚜室内毒力及田间防效   总被引:1,自引:0,他引:1  
王芳  陈佳斌  刘秉阳  牛浩  刘畅  何嘉  张蓉 《植物保护》2021,47(3):294-298
为了明确5种药剂对枸杞棉蚜的适宜施药剂量,开展了室内毒力测定和田间药效试验。结果表明,1%甲维盐EC对枸杞棉蚜的毒力最高,50%噻虫嗪WG毒力最低,24 h LC50分别为2.44 mg/L和1 875.69 mg/L。5种药剂毒力大小依次为甲维盐>啶虫脒>吡蚜酮>呋虫胺>噻虫嗪。田间试验结果表明,随着施药时间的延长,5种药剂不同剂量处理的虫口数量均显著下降,施药后7 d,各处理对枸杞棉蚜防效分别达94.13%~99.84%,且各剂量处理均对枸杞树安全。5种药剂推荐使用剂量分别为:5%啶虫脒EC 25.0 mg/L以上,30%呋虫胺SC 50.0~100.0 mg/L,50%噻虫嗪WG 100.0~125.0 mg/L,25%吡蚜酮WP 83.3~125.0 mg/L,1%甲维盐EC 5.6~8.3 mg/L。  相似文献   

12.
N‐(4‐phenoxyphenyl)‐2‐pyridinecarboxamide (1) was synthesized from commercially available materials and its ovicidal and larvicidal activity against Cydia pomonella (L) was tested. The compound showed a LC50 of 0.98 mg ml−1 when eggs less than 24 h were sprayed using a Potter Tower, but it had no effect when eggs older than this were sprayed. The compound did not have larvicidal activity when larvae were treated with 1200 µg g−1. However, the larval head capsules were smaller than those in the controls when treated at this concentration. To assess its possible juvenile‐hormone‐like activity, the compound was topically applied to young pupae of Tribolium confusum duVal, where it produced clear juvenilization effects, which were dependent on the applied dose. © 2000 Society of Chemical Industry  相似文献   

13.
The cardiac glycoside, digitoxin, from Digitalis purpurea L (Scrophulariaceae), a cardiac glycosidal (cardenolide) extract from Calotropis procera (Ait) R Br (Asclepiadaceae), azadirachtin and neem oil from Azadirachta indica A Juss (Meliaceae) were tested for their effects against larvae and adult stages of the camel tick, Hyalomma dromedarii Koch (Acari: Ixodidae). The contact LC50 values of the first three materials against adults were 4.08, 9.63 and >40.7 microg cm(-2), respectively, whereas the dipping LC50 values of the four materials were 409.9, 1096, >5000 and >5000 mg litre(-1), respectively. Contact and dipping LC50 values of the extract and azadirachtin against larvae were 6.16, >20.3 microg cm(-2) and 587.7 and >2500 mg litre(-1), respectively. Azadirachtin had no effects on egg production or feeding of adults up to 5000 mg litre(-1); however at 2500 mg litre(-1), it caused significant reduction in feeding activity of larve, prolonged the period for moulting to nymphal stage, and caused 60% reduction in moultability. Results of the two cardiac glycoside materials are comparable with those of several commercial acaricides. The risks and benefits associated with the use of cardiac glycosides are considered.  相似文献   

14.
Zhong G  Liu J  Weng Q  Hu M  Luo J 《Pest management science》2006,62(10):976-981
The activity of rhodojaponin-III (R-III), a grayanoid diterpene compound isolated from Rhododendron molle G. Don flowers, was determined under laboratory and field conditions as an antifeedant, stomach poison, contact toxicant and insect growth inhibitor against Pieris rapae (L.) larvae. The median antifeedant concentration (AFC(50)) values in no-choice leaf disc tests were 1.16 and 15.85 mg L(-1) at 24 h after treatment when tested against third and fifth instars respectively. The median lethal concentration (LC(50)) values in leaf disc tests were 2.84 and 9.53 mg L(-1) at 96 h after treatment against third and fifth instars respectively. R-III showed an almost 30 times higher contact toxicity against third instars than for fifth instars, and the median lethal dose (LD(50)) values for topical application were 1.18 and 34.09 mg kg(-1) at 72 h after treatment respectively. R-III disrupted the development of larvae to pupae or adults with median concentration for inhibiting growth (IC(50)) values of only 1.36 mg L(-1) for third instars and 11.28 mg L(-1) for fifth instars. In field trials, a greater than 80% reduction in the adjusted larval numbers was obtained against P. rapae 14 days after treatment when Rhodo 0.1% EC, a commercial botanical insecticide based on R-III, was applied at both 937.5 and 625 mL ha(-1). These results suggest that further research to develop R-III, and extracts from R. molle, as biorational pesticides or as lead compounds for integrated pest management deserve consideration.  相似文献   

15.
为筛选出用于防治棕榈蓟马的有效药剂,采用玻璃残留处理法测定了5种药剂对蔬菜上棕榈蓟马的室内毒力,并进行了田间药效试验。室内毒力测定结果表明,杀虫活性最高的是乙基多杀菌素,其48h的LC50值为0.19mg/L;其次是阿维菌素、溴氰虫酰胺和啶虫脒,LC50值为54.45~76.48mg/L,呋虫胺的毒力最低。田间试验结果表明,6%乙基多杀菌素悬浮剂和1.8%阿维菌素乳油对棕榈蓟马药后1~14d的防效均达90.88%以上,明显高于其他3种药剂。6%乙基多杀菌素悬浮剂是防治棕榈蓟马的首选药剂,推荐轮换使用1.8%阿维菌素乳油和10%溴氰虫酰胺可分散油悬浮剂。  相似文献   

16.
BACKGROUND: Infestation by stored-product pests causes serious losses in food and feed commodities. Among possible strategies against these pests, which aim to reduce the use of synthetic insecticides, including fumigants, natural insecticides produced by plants represent one of the most promising approaches for their ecochemical control. Three six-carbon and nine-carbon aldehydes, natural plant volatiles produced by the plant lipoxygenase pathway, were tested for their insecticidal activity against five species of stored-product beetles in feeding, fumigation and combined bioassays. RESULTS: The compounds (2E,6Z)-nonadienal, (2E)-nonenal and (2E)-hexenal were incorporated into feeding discs in feeding bioassays or evaporated from filter paper in closed glass chambers in fumigation tests. Beetle sensitivity to aldehydes differed according to the different treatments. The highest activity was obtained by (2E)-hexenal in fumigation tests, with the LC(50) ranging from 4 to 26 mg L(-1), while (2E, 6Z)-nonadienal was the most effective in feeding tests, giving LD(50)s ranging from 0.44 to 2.76 mg g(-1) when applied to feeding discs. Fumigation tests in the presence of wheat grains confirmed that (2E)-hexenal was the most effective compound, with a calculated LC(99) ranging from 33 to 166 mg L(-1). CONCLUSION: The results of both feeding and fumigation tests indicated that natural plant aldehydes are potential candidates to control stored-product beetles.  相似文献   

17.
3种环境友好型药剂对西花蓟马的室内毒力与田间防效   总被引:3,自引:0,他引:3  
测定了3种杀虫剂对西花蓟马的室内毒力和田间防效。室内生物测定结果表明,多杀菌素、甲氨基阿维菌素苯甲酸盐、阿维菌素对西花蓟马成虫的LC50值为0.050~2.887mg/L,对西花蓟马若虫的LC50值为0.040~0.457mg/L;田间药效试验表明,田间防治西花蓟马时推荐使用剂量(防效>80%)分别为:2.5%多杀菌素悬浮剂30~60g/667m2,1%甲氨基阿维菌素苯甲酸盐乳油30~60g/667m2,1.8%阿维菌素乳油不可低于75g/667m2。  相似文献   

18.
为有效防控厚皮甜瓜细菌性果斑病的发生,提出一套综合防控技术,通过田间开展各单项防控技术的重要性试验,建立标准化综合防控技术体系。结果表明:各单项技术可提高对细菌性果斑病的防效。与对照相比,72%农用硫酸链霉素可溶粉剂浸种可使防效提高16%,病果率降低3%;标准化喷药能使防效提高17%以上,病果率降低3.1%;整枝打杈前后进行防控能使防效提高39%以上;厚皮甜瓜整个生育期不浇水,能够减少病果的数量;在此基础上组装而成的标准化综合防控技术体系防效达89.2%以上,病果率仅为2%。  相似文献   

19.
氟啶虫胺腈对棉蚜的生物活性及对棉花的安全性   总被引:4,自引:0,他引:4  
本文通过叶片浸渍法研究了氟啶虫胺腈对棉蚜的室内活性,同时分析了其对棉花的安全性。室内毒力测定结果表明,氟啶虫胺腈处理棉蚜24h的LC50和LC90为1.98mg/L和26.02mg/L,显著低于吡虫啉的8.69mg/L和132.68mg/L,毒效比达4.39;处理48h后,氟啶虫胺腈对棉蚜仍表现出很高的杀虫活性,且显著高于吡虫啉。棉花安全性试验结果表明,在使用浓度40~160g/hm2范围内喷施500g/kg氟啶虫胺腈水分散粒剂,对棉花不同时期的叶色、株高、果枝层以及棉蕾脱落都未造成显著性的影响。  相似文献   

20.
本文研究了苯甲酰基苯脲类化合物克幼脲对玉米螟的毒力及药效。室内测定表明,克幼脲对玉米螟低龄幼虫的胃毒毒力LC50=2.39mg/kg,对玉米螟卵也表现了一定的抑制效应;田间试验证明,克幼脲复配4号对玉米螟的防效达94.2%。  相似文献   

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