Hostname: page-component-745bb68f8f-kw2vx Total loading time: 0 Render date: 2025-01-09T12:25:45.757Z Has data issue: false hasContentIssue false
  • English
  • Français

Comparisons of Dihydroxybenzenes and Paraquat

Published online by Cambridge University Press:  12 June 2017

E. J. Hogue  and
G. F. Warren
E. J. Hogue
Affiliation:
Department of Horticulture, Purdue University
G. F. Warren
Affiliation:
Department of Horticulture, Purdue University
Get access Rights & Permissions [Opens in a new window]

Abstract

Although similar in mode of action, 1,2-dihydroxybenzene (catechol) and 1,1′-dimethyl-4,4′bipyridinium ion (paraquat) at different levels were required to kill plants. Both chemicals were fast-acting, they both required light to be active, and herbicides that inhibit photosynthesis protected the plants temporarily against the action of both compounds. Paraquat and catechol had additive effects on black nightshade (Solanum nigrum L.) but not on redroot pigweed (Amaranthus retroflexus L.). Catechol protected redroot pigweed against the action of paraquat.

Type
Research Article
Information
Weed Science , Volume 18 , Issue 1 , January 1970 , pp. 179 - 182
Copyright
Copyright © 1970 Weed Science Society of America 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

1. Beevers, Harry. 1961. Respiratory Metabolism in Plants. Row, Peterson and Company. White Plains, New York. 232 p.Google Scholar
2. Fujimori, E. and Tavla, M. 1965. Interaction between chlorophyll and hydroquinone. Nature 208:78–79.CrossRefGoogle Scholar
3. Funderburk, H. H. Jr. and Laurence, J. M. 1964. Mode of action and metabolism of diquat and paraquat. Weeds 12: 259–264.Google Scholar
4. Hilton, J. L., Monaco, T. J., Moreland, D. E., and Gentner, W. A. 1964. Mode of action of substituted uracil herbicides. Weeds 12:129–131.CrossRefGoogle Scholar
5. Homer, R. F., Mees, G. C., and Tomlinson, T. E. 1960. The stereochemistry of the bridged quaternary salts of 2,2′-bipyridyl. J. Chem. Soc. p. 2498–2503.Google Scholar
6. Homer, R. F., Mees, G. C., and Tomlinson, T. E. 1960. Mode of action of dipyridyl quaternary salts as herbicides. J. Sci. Food Agr. 11:309–315.Google Scholar
7. Jagendorf, A. T. and Avron, M. 1959. Inhibitors of photosynthetic phosphorylation in relation to electron and oxygen transport pathways of chloroplasts. Arch. Biochem. Biophys. 80:246–257.Google Scholar
8. Mees, G. C. 1960. Experiments on the herbicidal action of 1,1′-ethylene-2, 2′-dipyridylium dibromide. Ann. Appl. Biol. 48:601–612.CrossRefGoogle Scholar
9. Mellor, R. A. and Salisbury, F. B. 1965. Influence of light regime on the toxicity and physiological activity of herbicides. Plant Physiol. 40:506–512.CrossRefGoogle ScholarPubMed
10. Slade, P. and Smith, A. E. 1967. Photochemical degradation of diquat. Nature 213:919–920.CrossRefGoogle Scholar
11. Thomson, R. H. 1964. Structure and reactivity of phenolic compounds, p. 1–32. In Harbone, J. B. (ed.) Biochemistry of Phenolic Compounds. Academic Press, London and New York.Google Scholar