Guidelines for Canadian Drinking Water Quality: Guideline Technical Document – Diuron

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Organization: Health Canada

Type: Guidelines

Date published: 1987-03 (edited March 1989)

Table of Contents

Guideline

The maximum acceptable concentration (MAC) for diuron in drinking water is 0.15 mg/L (150 mg/L).

Identity, Use and Sources in the Environment

Diuron is a substituted urea-based herbicide used in Canada in 1986 in moderately low quantities (in the range 10 000 to 50 000 kg). Footnote 1 It is employed principally for the control of vegetation in non-crop areas, including irrigation and drainage ditches.Footnote 1 Diuron is a non-ionic compound with moderate water solubility of 22 to 42 mg/L at 20ºC. Its hydrolysis rate is negligible at neutral pH but increases under strongly acidic or alkaline conditions. Footnote 2 It is stable to oxidation and breakdown, persisting in soils for a full season or longer. Footnote 3 It has a log octanol-water partition coefficient of 2.6, which is considered low to moderate. It is adsorbed to soils to some degree, with a moderate soil-water partition coefficient of 485. Footnote 4 The U.S. Environmental Protection Agency has ranked diuron fairly high -- as a Priority B chemical -- with respect to potential for groundwater contamination, Footnote 5 and it also rates highly in Agriculture Canada's ranking of potential leaching agents. Footnote 6

Exposure

Diuron has not often been included in Canadian water monitoring surveys; it has been detected once in a survey of 15 private wells in Ontario. Footnote 7 In the United States, diuron was detected in 0.03% of more than 900 groundwater samples. It was found in the low parts per billion range (2 to 3 mg/L) in California wells as a result of agricultural practices. Footnote 8 The theoretical maximum dietary intake of diuron for an adult Canadian would be about 0.48 mg/d, or 0.007 mg/kg bw per day, assuming that every crop for which it is registered contained it at the maximum residue level (MRL). Footnote 9 However, its use pattern indicates that it is seldom used on crops, especially wheat and potatoes, which contribute 70% of the theoretical daily intake. Footnote 10 No actual residue levels in foods are available, as diuron was not included in total diet surveys in either Canada or the United States.

Analytical Methods and Treatment Technology

Diuron may be monitored in water by extraction into hexane, hydrolysis to the aniline derivative, quantification by gas/liquid chromatography and Hall conductivity detection. The detection limit using this method is 0.1 mg/L. Footnote 11 Granular activated carbon and powdered activated carbon are effective in removing up to 90% of diuron from drinking water. Footnote 12

Health Effects

Diuron is absorbed from the gastrointestinal and respiratory systems. In humans, it is metabolized within hours by hydroxylation and N-dealkylation, then excreted via the urine. Footnote 13 In rats and dogs, one-sixth to one-half the total eliminated was found in the faeces. Footnote 14 Following ingestion of diuron for nine months to two years by rats and dogs, little storage was observed in any tissue; the highest levels were seen in liver and kidney.Footnote 14

Diuron is of low acute toxicity. Juveniles and animals on protein-deficient diets are more susceptible than adults to the toxic effects of diuron, based on LD50 results.Footnote 13 Ingestion by a woman of a single dose of diuron at 38 mg/kg bw had no apparent effect.Footnote 13 In animals, the principal toxic effects of chronic ingestion of diuron are weight loss and abnormalities in blood, liver and spleen.Footnote 13

Two chronic feeding studies have been conducted with diuron, which was administered in the diet for two years to groups of two male and three female beagle dogs at dose levels corresponding to 0, 0.625, 3.125, 6.25 or 31.25 mg/kg bw per day, and to 35 rats of each sex at dose levels corresponding to 0, 1.25, 6.25, 12.5 or 125 mg/kg bw per day.Footnote 8,Footnote 13,Footnote 14 At 125 ppm (3.125 mg/kg bw in dogs and 6.25 mg/kg bw in rats), traces of abnormal blood pigments were observed in a few animals but were not statistically significant. At 250 ppm and above (6.25 mg/kg bw in dogs and 12.5 mg/kg bw in rats), haematological alterations, weight loss, haemosiderosis of the liver and erythroid hyperplasia were observed. The no-observed-adverse-effect level (NOAEL) was 125 ppm, or 3.125 mg/kg bw in dogs and 6.25 mg/kg bw in rats. Although there was no evidence of carcinogenicity in these experiments, no firm conclusions can be drawn because the studies had methodological flaws.

Diuron was not mutagenic in most microbial tests with or without metabolic activation. Footnote 15 One positive result was reported, in Salmonella typhimurium, with metabolic activation. Footnote 16 Diuron was negative in two in vitro mammalian test systems, for forward gene mutations in Chinese hamster ovary cells and for unscheduled DNA synthesis in rat hepatocytes. Footnote 17 However, clastogenic effects were observed in an in vivo test on rats.Footnote 17

Reproduction was not affected in a three-generation rat study with dietary levels equivalent to 6 mg/kg bw per day; however, this dose was slightly foetotoxic, causing reduction of body weights in the F2 and F3 litters.Footnote 8,Footnote 13 Diuron was not teratogentic but was foetotoxic in rats receiving 250 mg/kg bw per day, with lowered foetal weights and minor rib and bone anomalies observed. The same effects were observed at 125 mg/kg bw per day but were not statistically significant.Footnote 18 The lowest-observed-adverse-effect level (LOAEL) was therefore 125 mg/kg bw per day.

Rationale

Based on evaluations by the Food Directorate of the Department of National Health and Welfare, Footnote 19 the acceptable daily intake (ADI) for diuron is derived as follows:

Formula

where:

  • 3.125 mg/kg bw per day is the NOAEL observed in a two-year dog study14 that was evaluated by the Food Directorate and considered to be the most suitable study on which to base an ADI. Body weight loss, increased liver weight, erythroid hyperplasia and decreased haematological values were observed at higher dosesFootnote 14,Footnote 19
  • 200 is the uncertainty factor assigned by the Food Directorate.

The maximum acceptable concentration (MAC) is derived from the ADI as follows:

Formula

where:

  • 0.0156 mg/kg bw per day is the ADI, as derived above
  • 70 kg is the average body weight of an adult
  • 0.20 is the proportion of total daily intake of diuron assigned to drinking water (theoretical maximum intake from food is 45% of the ADI)
  • 1.5 L/d is the average daily consumption of drinking water for an adult.

References

Footnotes

Footnote 1

Environment Canada/Agriculture Canada. Pesticide Registrant Survey, 1987 report. Commercial Chemicals Branch, Conservation and Protection, Environment Canada, Ottawa (1987).

Return to footnote 1 referrer

Footnote 2

Spencer, E.Y. Guide to chemicals used in crop protection. 7th edition. Research Branch, Agriculture Canada, Ottawa (1982).

Return to footnote 2 referrer

Footnote 3

Ashton, F.M. Persistence and biodegradation of herbicides. In: Biodegradation of pesticides. F. Matsumura and C.R. Krishna Murti (eds.). Plenum Press, New York, NY. p. 117 (1982).

Return to footnote 3 referrer

Footnote 4

Hamaker, J.W. The interpretation of soil leaching experiments. In: Environmental dynamics of pesticides. R. Haque and V.H. Freed (eds.). Plenum Press, New York, NY. p. 115 (1975).

Return to footnote 4 referrer

Footnote 5

U.S. Environmental Protection Agency. EPA draft final list of recommendations for chemicals in the National Survey for Pesticides in Groundwater. Chem. Regul. Rep., 9(34): 988 (1985).

Return to footnote 5 referrer

Footnote 6

Agriculture Canada. Pesticide priority scheme for water monitoring program. Unpublished report, Pesticide Directorate (1986). (Published as Backgrounder, No. 89-01, Issues, Planning and Priorities Division, 1989.)

Return to footnote 6 referrer

Footnote 7

Hiebsch, S.C. The occurrence of thirty-five pesticides in Canadian drinking water and surface water. Unpublished report prepared for Environmental Health Directorate, Department of National Health and Welfare, January (1988).

Return to footnote 7 referrer

Footnote 8

U.S. Environmental Protection Agency. Diuron health advisory. Office of Drinking Water (1987).

Return to footnote 8 referrer

Footnote 9

Department of National Health and Welfare. National pesticide residue limits in foods. Chemical Evaluation Division, Food Directorate, Ottawa (1986).

Return to footnote 9 referrer

Footnote 10

Department of National Health and Welfare. Food consumption patterns report. Nutrition Canada, Bureau of Nutritional Sciences, Health Protection Branch (1977).

Return to footnote 10 referrer

Footnote 11

Frank, R., Clegg, B.S., Ripley, B.D. and Braun, H.E. Investigations of pesticide contamination in rural wells, 1979-1984, Ontario, Canada. Arch. Environ. Contam. Toxicol., 16: 9 (1987).

Return to footnote 11 referrer

Footnote 12

El-Dib, M.A. and Aly, O.A. Removal of phenylamide pesticides from drinking water. II. Adsorption on powdered carbon. Water Res., 11:617 (1977).

Return to footnote 12 referrer

Footnote 13

Hayes, W.J., Jr. Pesticides studied in man. Williams and Wilkins,Baltimore, MD (1982).

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Footnote 14

Hodge, H.C., Downs, W.L., Panner, B., Smith, D., Maynard, E., Clayton, J., Jr. and Rhodes, R. Oral toxicity and metabolism of diuron in rats and dogs. Food Cosmet. Toxicol., 5: 513 (1967).

Return to footnote 14 referrer

Footnote 15

Grutman, G., Schoofs, L., Lontie, J.-F. and van Larebeke, N. The mutagenicity in prokaryotes of herbicides. Residue Rev., 91: 1 (1984).

Return to footnote 15 referrer

Footnote 16

Seiler, J.P. Herbicidal phenylalkylureas as possible mutagens. I. Mutagenicity tests with some urea herbicides. Mutat. Res., 58: 353 (1978).

Return to footnote 16 referrer

Footnote 17

Dupont de Nemours & Co. Mutagenicity studies with diuron. Salmonella test, No. HLR 471-84 (7185); CHO/HGPRT forward gene mutation assay, H.R. No. 282-85 (06/28/85); unscheduled DNA synthesis test in primary rat hepatocytes, HLR No. 349-85; and in vivo cytogenetic test, No. 36685 (1985), cited in reference 8.

Return to footnote 17 referrer

Footnote 18

Khera, K.S., Whalen, C., Trivett, G. and Ongers, G. Teratogenicity studies on pesticide formulations of dimethoate, diuron, and lindane in rats. Bull. Environ. Contam. Toxicol., 22: 522 (1979).

Return to footnote 18 referrer

Footnote 19

Department of National Health and Welfare. Memorandum from D. Clegg, Food Directorate, to P. Toft, Environmental Health Directorate, August 6 (1986).

Return to footnote 19 referrer

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