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Penetration of 3–Amino–1,2,4–triazole in Canada Thistle and Field Bindweed

Published online by Cambridge University Press:  12 June 2017

R. A. Herrett  and
A. J. Linck
R. A. Herrett
Affiliation:
Department of Plant Pathology and Botany, University of Minnesota Union Carbide Chemicals Company, Union Carbide Research Station; Clayton, North Carolina
A. J. Linck
Affiliation:
Department of Plant Pathology and Botany, Institute of Agriculture, University of Minnesota, St. Paul, 1, Minnesota
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Extract

The compound, 3–amino–1,2,4–triazole (amitrole), has been used as an herbicide against different weed species with varying degrees of success. In the field, Canada thistle (Cirsium arvense (L.) Scop.) has been found relatively susceptible while field bindweed (Convolvulus arvensis L.) has been found relatively resistant to the action of amitrole. The reason(s) for this difference in sensitivity is not known. Because penetration of amitrole from the surface of the leaf to the interior is the first step in the chain of events leading to a response from a chemical by the treated plant, the nature of this process was examined.

Type
Research Article
Information
Weeds , Volume 9 , Issue 2 , April 1961 , pp. 224 - 230
Copyright
Copyright © 1961 Weed Science Society of America 

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References

Literature Cited

1. American Cyanamid Company. Amino triazole technical data sheet. February, 1956.Google Scholar
2. Anderson, O. Studies on the absorption and translocation of amitrole (3–amino–1,2,4–triazole) by nut grass (Cyperus rotundus L.). Weeds 6:370–385. 1958.CrossRefGoogle Scholar
3. Ashton, F. M. Absorption and translocation of radioactive 2,4–D in sugarcane and bean plants. Weeds 6:257–262. 1958.CrossRefGoogle Scholar
4. Fang, S. C. Absorption, translocation and metabolism of 2,4-D–1–C14 in peas and tomato plants. Weeds 6:179–186. 1958.CrossRefGoogle Scholar
5. Fang, S. C. and Butts, J. S. Studies in plant metabolism. III. Absorption, translocation and metabolism of radioactive 2,4–D in corn and wheat plants. Plant Physiol. 29:56–60. 1954.CrossRefGoogle Scholar
6. Freed, V. H., and Montgomery, M. The effect of surfactants on foliar absorption of 3–amino–1,2,4–triazole. Weeds 6:386–389. 1958.CrossRefGoogle Scholar
7. Green, F. C., and Feinstein, R. N. Quantitative estimation of 3–amino–1,2,4–triazole. Anal. Chem. 29:1658–1660. 1957.CrossRefGoogle Scholar
8. Lee, O. C. Two years results with amino triazole on Canada thistles. Res. Rep. NCWCC 12:5. 1955.Google Scholar
9. Racussen, D. The metabolism and translocation of 3–amino–triazole in plants. Arch. Biochem. Biophys. 74:106–113. 1958.CrossRefGoogle Scholar
10. VanOverbeek, J. Absorption and translocation of plant growth regulators. Ann. Rev. Plant Physiol. 7:355–372. 1956.CrossRefGoogle Scholar
11. Weaver, R. J., and DeRose, R. H. Absorption and translocation of 2,4–dichlorophenoxyacetic acid. Bot. Gaz. 107:509–521. 1946.CrossRefGoogle Scholar
12. Wiese, A. F., and Rea, H. E. Field bindweed (Convolvulus arvensis) control with heavy rates of translocated herbicides on Pullman silty clay loam. Res. Rep. NCWCC 12:10. 1955.Google Scholar