1977
DOI: 10.5962/bhl.title.78801
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Laboratory and field evaluation of several organochlorine and organophosphorus compounds for control of imported fire ants

Abstract: Eleven organochlorine and twelve organophosphorus pesticides and one antibiotic were selected from laboratory screening tests for field evaluation in baits for control of the red imported fire ant, Solenopsis invicta Buren.

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Cited by 6 publications
(7 citation statements)
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“…The LT 15 and LT 50 CLs did not overlap for hydramethylnon based on moribund/dead data obtained from the two separate delayed toxicity tests (Tables 4 and 5). Variation in delayed toxicity among separate tests has occurred with mirex and hydramethylnon baits (Banks et al 1977, Vander Meer et al 1982). The differences may be attributed to many unspeciÞed factors among different studies (e.g., temperature, ant size, and nutritional needs) that could contribute to experimental variation.…”
Section: Resultsmentioning
confidence: 97%
“…The LT 15 and LT 50 CLs did not overlap for hydramethylnon based on moribund/dead data obtained from the two separate delayed toxicity tests (Tables 4 and 5). Variation in delayed toxicity among separate tests has occurred with mirex and hydramethylnon baits (Banks et al 1977, Vander Meer et al 1982). The differences may be attributed to many unspeciÞed factors among different studies (e.g., temperature, ant size, and nutritional needs) that could contribute to experimental variation.…”
Section: Resultsmentioning
confidence: 97%
“…N-sec-Butyl-phydroxybenzamide (2d): mp 157-158 °C (chloroform); 70% yield; NMR (acetone-d6) 0.9 (t, 3 ), 1.2 (d, 3 ), 1.6 (m, 2 ), 4.1 (m, 1 H), 6.9 (d, 2 H), 7.8 (m, 3 H); mass spectrum m/e 193 (M+). N-n-Amyl-p-hydroxybenzamide (2e): mp 108-110 °C (ethanol); 84% yield; 1H NMR (acetone -d6) 0.93 (5 ), 1.4 (m, 4 ), 3.51 (m, 2 H), 6.8 (d, 2 H), 7.8 (m, 3 H s imported fire ant toxicant classification system (Banks et al , 1977).…”
Section: Methodsmentioning
confidence: 99%
“…Of the approximately 800 organophosphorous compounds that have been evaluated as possible imported fire ant toxicants, only 10 have exhibited delayed toxicity. All 10 are halogenated phosphorothionates (Banks et al, 1977). A comparison of the ester phosphorothionate derivatives (4) to the amide derivative (3) (Table III) indicates that the toxicities of the 0.1% solutions of the amides were only slightly more toxic than those of corresponding ester derivatives to the imported fire ant, but substitution of the amide group for a ester group greatly enhanced the delayed killing property of the phosphorothionates.…”
Section: -78ppmmentioning
confidence: 99%
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“…uated as possible imported fire ant toxicants, only 10 have exhibited delayed toxicity. All 10 are halogenated phosphorothionates (Banks et al, 1977). A comparison of the ester phosphorothionate derivatives (4) to the amide derivative (3) (Table III) indicates that the toxicities of the 0.1% solutions of the amides were only slightly more toxic than those of corresponding ester derivatives to the imported fire ant, but substitution of the amide group for a ester group greatly enhanced the delayed killing property of the phosphorothionates.…”
mentioning
confidence: 99%