几丁质抑制剂和Abg-6178对马铃薯甲虫的防治作用,1991

Donald W. Barry, J. Bowman
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引用次数: 0

摘要

所有的生物测定都采用了一种实验室菌株的幼虫,该菌株生长在温室种植的“诺兰德”土豆上,年龄为36±12小时。对球孢白僵菌(Balsamo) Vuillemin进行了技术粉末(ABG-6178)和实验室气生分生孢子的测定。从感染ABG-6178的成年科罗拉多马铃薯甲虫尸体中分离出真菌后,在Sabouraud’s葡萄糖琼脂上培养10 ~ 20 d。以试验浓度浸泡马铃薯末端小叶(约10 cm2) 4 s。用润湿剂Tween 80(0.05%浓度)配制所有稀释液。对照组仅用0.05% Tween 80处理。处理后的叶片在吸水纸上晾干约60秒,然后放入单独的实验室风干。然后用驼毛刷将四到五个幼虫放在每片处理过的叶子上。实验重复2 ~ 4次。实验室由两个堆叠的60 x 20 mm塑料培养皿组成。培养皿顶部铺有湿润的滤纸。在培养皿底部钻一个洞,让叶柄延伸到培养皿底部,培养皿中装有蒸馏水,以保持叶片膨胀。在23°C、70-80% RH和18:6 L:D条件下,实验物保存在生长室中。48小时后更换叶片,此后视需要更换。暴露3 ~ 7 d后每隔24 h计算一次死亡率。对触觉刺激没有反应的个体被认为已经死亡。数据用雅培公式校正,并用概率分析(pol - pc)进行分析。并非所有的治疗方法每天都进行检测。
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Leaf-Dip Bioassays of Chitin Inhibitors and Abg-6178 for Control of Colorado Potato Beetle on Potatoes, 1991
All bioassays used larvae aged 36 ± 12 h from a laboratory strain of Colorado potato beetles reared on greenhouse-grown ‘Norland’ potatoes. The entomopathogen Beauveria bassiana (Balsamo) Vuillemin was assayed as both a technical powder (ABG-6178) and as aerial conidia grown in the laboratory. The fungus was cultured for 10 to 20 d on Sabouraud‘s dextrose agar after isolation from adult Colorado potato beetle cadavers previously infected with ABG-6178. Treatments were applied by submersing terminal potato leaflets (of about 10 cm2) for 4 s in a test concentration. A wetting agent, Tween 80 (0.05% concentration), was used to prepare all dilutions. Controls were treated with 0.05% Tween 80 alone. Treated leaves were allowed to drain on absorbent paper for about 60 s and placed into individual assay chambers to air dry. Four to five larvae were then placed on each treated leaf with a camel hair brush. Assays were repeated 2 to 4 times. Assay chambers were made of two stacked 60 x 20 mm plastic petri dishes. The top petri dish was lined with moist filter paper. A hole drilled through the dish base allowed the leaf petiole to extend into the lower petri dish which held a distilled water reservoir to maintain leaf turgor. Assays were kept in a growth chamber at 23°C, 70-80% RH and 18:6 L:D. Leaves were replaced after 48 h and, thereafter, as necessary. Mortality was counted at 24 h intervals after 3 to 7 d of exposure. Individuals not responding to tactile stimulation were considered dead. Data were corrected with Abbott‘s formula and analyzed using probit analysis (POLO-PC). Not all treatments were assayed on each day.
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