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1.
Environ Pollut ; 61(2): 127-55, 1989.
Article in English | MEDLINE | ID: mdl-15092368

ABSTRACT

Aldicarb is a soil-applied systemic pesticide the USEPA is now considering banning in the USA. Aldicarb is fairly rapidly oxidized to the sulfoxide, with a half-life of approximately 7 days in some soils, and much more slowly to the sulfone (pH-dependent with half-lives varying from a few minutes at a pH of > 12 to approximately 560 days at a pH of 6.0). Persistence, carry-over and translocation vary with soil and environmental conditions. Drainage aquifers and drinking water wells are known to be susceptible to contamination, levels of approximately 550 ppb have been recorded. Foods are also known to take up the pesticide; levels of 600 ppb have been found in potatoes.

2.
Environ Health Perspect ; 72: 267-81, 1987 Jun.
Article in English | MEDLINE | ID: mdl-3304999

ABSTRACT

Aldicarb, 2-methyl-2-(methylthio)propionaldehyde-O-methylcarbamoyloxime, is an oxime carbamate insecticide manufactured by the Union Carbide Corporation and sold under the trade name Temik. It is a soil-applied systemic pesticide used against certain insects, mites, and nematodes, and is applied below the soil surface for absorption by plant roots. It is generally applied to the soil in the form of 5, 10, or 15% granules, and soil moisture is essential for the release of the toxicant. Uptake by plants is rapid. Aldicarb is currently registered for use on cotton, sugar beets, sugar cane (Louisiana only), potatoes, sweet potatoes, peanuts, oranges, pecans (Southeast only), dry beans, soybeans, and ornamental plants. Home and garden use is not permitted. Discovery of aldicarb and its oxidative sulfoxide and sulfone metabolites in well or ground water in Florida, Wisconsin, and New York, and accidental poisonings from ingesting contaminated watermelons and cucumbers in the South and West have spurred interest and concern about this pesticide. The primary mechanism of toxic action of aldicarb is cholinesterase inhibition. However, unlike the relatively irreversible anticholinesterase activity of the organophosphate pesticides, the carbamylation process which produces the anti-AChE action is quickly reversible. Aldicarb is readily absorbed through both the gut and the skin, but is rapidly metabolized and excreted in the urine almost completely within 24 hr. Although it is acutely toxic to humans and laboratory animals, aldicarb is not known to be carcinogenic, teratogenic, conclusively mutagenic, or to produce other long-term adverse health effects. In cases of accidental poisoning, the cholinergic symptoms have generally subsided within 6 hr, with no side effects or complications.


Subject(s)
Aldicarb/toxicity , Insecticides/toxicity , Aldicarb/metabolism , Aldicarb/poisoning , Animals , Cholinesterase Inhibitors , Epidemiologic Methods , Humans , Lethal Dose 50 , Mammals , Mutagens , Neoplasms, Experimental/chemically induced , Receptors, Muscarinic/drug effects , Receptors, Nicotinic/drug effects , Reproduction/drug effects , Teratogens
3.
Toxicol Ind Health ; 3(1): 5-69, 1987 Mar.
Article in English | MEDLINE | ID: mdl-3590208

ABSTRACT

Pure pentachloronitrobenzene (PCNB) is a colorless crystalline solid (Worthing, 1983). The commercial product may have a light-yellow to cream color with a musty odor (Hartley and Kidd, 1983). It is practically insoluble in a number of organic solvents. The compound is reasonably stable but may undergo hydrolysis in a strong alkaline medium (Hartley and Kidd, 1983). In 1983, Olin Corp., Leland, MS, was the only manufacturer of PCNB in the United States (SRI, 1984; Hartley and Kidd, 1983). No data for U.S. production volume for this chemical are available, but recent production source data (USITC, 1985; SRI, 1985) suggest that this chemical is no longer commercially produced in the United States. The primary usage of PCNB is as a soil fungicide for a wide variety of crops and in seed treatment (Worthing, 1983; Hartley and Kidd, 1983). The fate of PCNB in water has not been comprehensively studied. Only qualitative data regarding fate and transport in water are available. The half-life of PCNB in the water phase was estimated to be 1.8 days. The two processes reported to be most responsible for the rapid decrease in PCNB concentration in water were volatilization and sorption to seston and biota, followed by sedimentation as detritus (Schauerte et al., 1982). Neither biodegradation nor photolysis appears to be a significant process for the loss of PCNB from water (Crosby and Hamadmad, 1971; Schauerte et al., 1982). The BCFs for PCNB in the golden orfe, Leucisens idus melanotus, and in rainbow trout, Salmo gairdneri, were reported to be 950-1130 and 260-590, respectively (Korte et al., 1978; Oliver and Niimi, 1985). It therefore appears that PCNB will moderately bioaccumulate in aquatic organisms. Pertinent data regarding the fate and transport of PCNB in air could not be located in the available literature as cited in the Appendix. Based on its physical properties and its behavior in other media, it would appear that PCNB will persist in the atmosphere because no known chemical/photochemical processes significantly degrade this chemical. Precipitation of particulate PCNB, especially of larger particle size and higher particle density, may remove some PCNB from the atmosphere. PCNB is persistent in soils. The two processes that are important in the loss of PCNB from soils are volatilization and biodegradation; biodegradation is more rapid in soils under anaerobic conditions than under aerobic conditions (Ko and Farley, 1969; Casley, 1968; Gile and Gillett, 1979; Cole and Metcalf, 1977).(ABSTRACT TRUNCATED AT 400 WORDS)


Subject(s)
Fungicides, Industrial/toxicity , Nitrobenzenes/toxicity , Animals , Carcinogens , Environmental Pollution , Mice , Neoplasms, Experimental/pathology , Nitrobenzenes/metabolism , Rats
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