Residue Reviews 1981
DOI: 10.1007/978-1-4612-5913-8_1
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Carbaryl: A Literature Review

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Cited by 33 publications
(13 citation statements)
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References 224 publications
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“…As pH is reduced, degradation by alkaline hydrolysis diminishes and other transformation processes influence fate of carbaryl (Kuhr and Dorough, 1976;Wolfe, Zepp, and Paris, 1978;Mount and Oehme, 1981) and malathion (Walker, 1976;Wolfe et al, 1977;Mulla, Mian, and Kawecki, 1981). Under laboratory conditions, effects of other transformation processes like photolysis, adsorption, microbial biotransformation, and volatilization can be controlled so that they do not contribute to degradation.…”
Section: Discussionmentioning
confidence: 97%
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“…As pH is reduced, degradation by alkaline hydrolysis diminishes and other transformation processes influence fate of carbaryl (Kuhr and Dorough, 1976;Wolfe, Zepp, and Paris, 1978;Mount and Oehme, 1981) and malathion (Walker, 1976;Wolfe et al, 1977;Mulla, Mian, and Kawecki, 1981). Under laboratory conditions, effects of other transformation processes like photolysis, adsorption, microbial biotransformation, and volatilization can be controlled so that they do not contribute to degradation.…”
Section: Discussionmentioning
confidence: 97%
“…Degradation of carbaryl and malathion is dominated by hydrolysis under certain conditions and is temperature and pH dependent (Aly and El-Dib, 1971;Kuhr and Dorough, 1976;Walker, 1976;Wolfe et al, 1977;Wolfe, Zepp, and Paris, 1978;Mount and Oehme, 1981;Mulla, Mian, and Kawecki, 1981). The objective of this research was to use results of published studies to estimate degradation models that predict half-life of carbaryl and malathion in freshwater over temperature and pH ranges relevant to western grasshopper-management programs.…”
Section: Introductionmentioning
confidence: 98%
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“…For instance, it is much more toxic to Hymenoptera than to other insect groups. Carbaryl degrades in ~ 2 wk and there is no evidence that it biologically accumulates in species in the ecosystems under study (Mount and Oehme 1981). A very important advantage of using carbaryl is that two previous studies (Barrett 1968, Suttman andBarrett 1979) have examined the effect of this insecticide at "normal" concentrations ( 10 x the level used in the present study) on arthropods in different ecosystems.…”
Section: Introductionmentioning
confidence: 91%
“…This study reports the potential of carbaryl, I-naphthyl N-methylcarbamate, product name Sevin, to kill L. salmonis and Atlantic salmon. Carbaryl was selected because there has been world-wide licensed use of this compound since 1958 for the control of over 150 major pests (MOUNT and OEHME 1981) and extensive toxicological reviews have been published (CRANMER 1986). Carbaryl, like dichlorvos, acts as an inhibitor of acetyl choline esterase and may only detach adult and pre-adult lice, though all stages possess this enzyme system (WALDAY and FONNUM 1989).…”
Section: Infestation Of Marine Culturedmentioning
confidence: 99%