CARBPHENOTHION JMPR 1976 Explanation Carbophenothion was evaluated at the 1972 JMPR (FAO/WHO 1973). Temporary tolerances were recommended for various fruits, nuts, vegetables, meat (fat), milk (fat), and olive oil. The tolerances are expressed as carbophenothion but apply to total residues including parent, its sulfoxide and sulfone and their corresponding oxygen analogs. Further work on plasma cholinesterase depression and a reproduction study were required for evaluation by the 1976 Joint Meeting. At the 1975 (Eighth) Session of the Codex Committee on Pesticide Residues, the delegation of the Netherlands requested re-evaluation of carbophenothion by the 1976 Joint Meeting. EVALUATION FOR ACCEPTABLE DAILY INTAKE Since the additional data required by the 1972 Joint Meeting were not available and there was no indication of intent to provide these data, the previously allocated temporary ADI was withdrawn. RESIDUES IN FOOD AND THEIR EVALUATION Country statements for the 1976 Joint Meeting were received from Australia, the Netherlands, and the United Kingdom. The information provided on current national uses of carbophenothion did not indicate a need for additional maximum residue limits for crops beyond those recommended by the 1972 Meeting. No additional data from supervised residue trials were available. The country statements included some information of interest on current use patterns, national tolerances and residue chemistry. USE PATTERN Information provided by the responding countries on current use patterns are shown in Table 1. FATE OF RESIDUES A submission from the United Kingdom reported research relating to injury to geese from the use of carbophenothion as a seed dressing on cereals. This use was subsequently withdrawn from certain areas in the U.K. The report included some collateral studies which were of interest with regard to possible residues in human foods. Carbophenothion and four esterase inhibiting degradation products were found at significant levels within the roots and bulbs of wheat grown from treated seeds, suggesting that carbophenothion has some systemic activity. Residues in the leaves were, however, very low. The identified inhibitors were carbophenothion sulphone, carbophenothion sulphoxide and the corresponding oxygen analogue and oxygen analogue sulphone. (Brown and Torpey, 1976). TABLE 1. National use patterns of carbophenothion Pre-harvest Application interval National(1) Country Crop Rate (days) tolerances (mg/kg) Australia fruits 0.05% emul. spray 21 1 vegetables 2 kg/ha 21 1 cattle, sheep 0.1% emul. spray 14(pre- 1 (fat basis) slaughter) pasture, forage 0.05% emul. spray 7(cutting or 0.1 milk and(2) grazing) milk products (fat) Netherlands prunes, peaches 14.75% before bloom 0.01(2) grapes aerosol and after (under glass) 0.06 g/m3 harvest (1) Maximum residue limits or tolerances as reported to the 1976 meeting. (2) Tolerance represents a change from national tolerances listed in 1972 monograph (FAO/WHO, 1973b). A laboratory experiment in the same report disclosed photolysis products after exposure to sunlight and UV radiation. In addition to the alteration products found in wheat seedlings, carbophenothion oxon and the insecticide ethion were identified after 130 hours' exposure to sunlight. (Machin et al., 1976). UV radiation at 254 nm produced four other related organophosphorus products. The experiments did not show whether, under field conditions, any of these compounds would constitute a significant part of the terminal residue on crops. METHODS OF RESIDUE ANALYSIS A comprehensive discussion of the methods available for carbophenothion and its oxidative metabolite residues in foods appears in the 1972 evaluation of this pesticide (FAO/WHO 1973b). Certain advances in carbophenothion methodology were called to the attention of the 1976 meeting. Jennings et al. (1975) describe an improved method for carbophenothion in avian tissues in which extraction with diethyl ether is followed by an alumina column clean-up. Alternative determinative steps specified in this method are TLC, GC with flame photometric detection and GC/MS. Brown and Weerasinghe (1976) further improved extraction of the oxidation products by substituting methanol for diethyl ether and modifying the chromatographic clean-up. The U.S. Food and Drug Administration multi-residue method for organophosphorus insecticides (FDA Pesticide Analytical Manual, Vol. I) will detect carbophenothion, the oxygen analogue, and the carbophenothion sulphone metabolites. APPRAISAL Three countries responded to requests for information for the re-evaluation of carbophenothion by the 1976 Joint Meeting. There was no indication that the scope of carbophenothion uses has increased since the 1972 evaluation. No additional data from supervised residue trials were available. There was no new information on residue chemistry which would justify any changes in the previously recommended maximum residue limits. Some new information on the nature of carbophenothion residues and on analytical methods was evaluated. EVALUATION Because the further information required by the 1972 Joint Meeting has not been supplied, the temporary ADI and temporary maximum residue limits then recommended are withdrawn. In the absence of an ADI, the temporary limits are converted to guideline levels. FURTHER WORK OR INFORMATION REQUIRED (before an acceptable daily intake can be allocated and maximum residue limits can be recommended) 1. Studies to substantiate the marked species difference in sensitivity to plasma cholinesterase depression. 2. An adequate reproduction study. DESIRABLE 1. Further elucidation of the nature of the terminal residues on crops, particularly as to possible presence under field conditions of photolysis products reported by Machin and coworkers. REFERENCES FAO/WHO. 1972 Evaluations of some pesticide residues in 1973 foods. FAO/AGP/1972/M/9/1. Brown, P.M. & Torpey, C.L. Determination of carbopheniothion 1976 residues in wheat plants grown from carbophenothion-treated seeds. Pest Infestation Control Laboratory, Ministry of Agriculture, Fisheries and Food, unpublished. Brown, P.M. & Weerasinghe, D.K. Evaluation, development and 1976 application of methods for extraction and analysis of carbophenothion and its metabolites from avian tissues. Unpublished report, Pest Infestation Control Laboratory, U.K., Ministry of Agriculture, Fisheries and Food. Jennings, D.M., Bunyan, P.J., Brown, P.M., Stanley, P.I., & Jones, 1975 F.J.S. Organophosphorus poisoning; a comparative study of the toxicity of carbophenothion to the Canada Goose, the Pigeon and the Japanese Quail. Pestic. Sci., 6:245-257. Machin, A.F., Quick, M.P., & Norman, I.M. Unpublished. 1976 Stanley, P.I., Brown, P.M., Martin, A.D., Steed, L.C., Westlake, 1976 G.E., Howells, L.C. & Machin, A.F. The avian toxicology of carbophenothion. Pest Infestation Control Laboratory and the Central Veterinary Laboratory, Ministry of Agriculture, Fisheries and Food, unpublished.
See Also: Toxicological Abbreviations Carbophenothion (ICSC) Carbophenothion (WHO Pesticide Residues Series 2) Carbophenothion (Pesticide residues in food: 1977 evaluations) Carbophenothion (Pesticide residues in food: 1979 evaluations) Carbophenothion (Pesticide residues in food: 1980 evaluations) Carbophenothion (Pesticide residues in food: 1983 evaluations)