{"title":"几丁质抑制剂和Abg-6178对马铃薯甲虫的防治作用,1991","authors":"Donald W. Barry, J. Bowman","doi":"10.1093/iat/18.1.372","DOIUrl":null,"url":null,"abstract":"\n 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.","PeriodicalId":13691,"journal":{"name":"Insecticide and Acaricide Tests","volume":"82 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Leaf-Dip Bioassays of Chitin Inhibitors and Abg-6178 for Control of Colorado Potato Beetle on Potatoes, 1991\",\"authors\":\"Donald W. Barry, J. Bowman\",\"doi\":\"10.1093/iat/18.1.372\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n 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.\",\"PeriodicalId\":13691,\"journal\":{\"name\":\"Insecticide and Acaricide Tests\",\"volume\":\"82 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insecticide and Acaricide Tests\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/iat/18.1.372\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insecticide and Acaricide Tests","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/iat/18.1.372","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.