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首页> 外文期刊>Industrial Crops and Products >Toxicity of quinones against two-spotted spider mite and three species of aphids in laboratory and greenhouse conditions.
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Toxicity of quinones against two-spotted spider mite and three species of aphids in laboratory and greenhouse conditions.

机译:在实验室和温室条件下,醌对两点红蜘蛛和三种蚜虫的毒性。

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摘要

Toxicities of the eight quinones were evaluated through leaf dip bioassays conducted against Tetranychus urticae, Myzus persicae, Myzocallis walshii, and Illinoia liriodendri. Based on LC50 values, plumbagin (LC50=0.001%) was the most active compound against T. urticae and ubiquinone Q0 (LC50=0.005%), plumbagin (LC50=0.010%), and dibromothymoquinone (LC50=0.012%) were the most active compounds against M. persicae. The most active compounds against M. walshii were juglone (LC50=0.011%) and ubiquinone Q0 (LC50=0.019%), whereas dibromothymoquinone (LC50=0.030%), plumbagin (LC50=0.033%) and ubiquinone Q0 (LC50=0.058%) were the most toxic to I. liriodendri. Ecotrol (positive control) was the least toxic compound (LC50=0.39%) against T. urticae and M. persicae (LC50=0.447%). Although the majority of the compounds tested were toxic to all four test species in residual bioassays, there was little overlap among the test species in terms of susceptibility to the compounds and interspecific differences were observed. Regarding structure-activity relationships for quinones, the addition of a hydroxyl group resulted in a significant increase in the toxicity of the 1,4-naphthoquinones, and those possessing a methyl group exhibited the highest levels of activity in T. urticae. The bromine atom at the 2- and 5-positions of the benzoquinone ring is crucial to the toxicity of the compounds against I. liriodendri. Toxicity was greatly affected not only by the number of hydroxyl groups, but also by their positions in the ring in the case of M. walshii. Juglone and plumbagin as residual toxins in the laboratory also reduced the population of two-spotted spider mites compared to EcoTrolTM (positive control) and the negative control in the greenhouse experiment. Some quinones tested may have potential as commercial insecticides and miticides, or alternatively, could serve as lead compounds for the development of more potent crop protection agents.
机译:通过对 Tetranychus urticae , Persicae persicae , Myzocallis walshii 和 Illinoia liriodendri 的叶浸生物测定法评估了八个醌的毒性。 / i>。根据LC 50 值,铅皮素(LC 50 = 0.001%)是抗 T活性最高的化合物。荨麻疹和泛醌Q 0 (LC 50 = 0.005%),李子苷(LC 50 = 0.010%)和二溴胸腺醌( LC 50 = 0.012%)是对抗 M的最具活性的化合物。波斯菊。对抗M的活性最高的化合物。 walshii 为juglone(LC 50 = 0.011%)和泛醌Q 0 (LC 50 = 0.019%),而二溴胸腺醌( LC 50 = 0.030%),李子(LC 50 = 0.033%)和泛醌Q 0 (LC 50 = 0.058%)对I最具毒性。 liriodendri 。 Ecotrol(阳性对照)是对 T的毒性最低的化合物(LC 50 = 0.39%)。荨麻疹和 M。 persicae (LC 50 = 0.447%)。尽管在残留生物测定中测试的大多数化合物对所有四个测试物种均具有毒性,但就化合物的敏感性而言,测试物种之间几乎没有重叠,并且观察到种间差异。关于醌的结构-活性关系,羟基的添加导致1,4-萘醌的毒性显着增加,而具有甲基的那些在T中表现出最高水平的活性。荨麻科。苯醌醌环的2-和5-位上的溴原子对于化合物对I的毒性至关重要。 liriodendri 。毒性不仅受羟基数的影响,而且在 M情况下也受其在环中位置的影响。 walshii 。与温室试验中的EcoTrol TM (阳性对照)和阴性对照相比,朱古隆和铅白蛋白作为残留毒素在实验室中也减少了两个斑点的红蜘蛛的数量。测试的某些醌可能具有商业杀虫剂和杀螨剂的潜力,或者可以用作开发更有效的农作物保护剂的先导化合物。

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