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Effect of Leaf Girdling and Rhizome Girdling on Glyphosate Transport in Quackgrass (Agropyron repens)

Published online by Cambridge University Press:  12 June 2017

Thomas B. Klevorn  and
Donald L. Wyse
Thomas B. Klevorn
Affiliation:
Dep. of Agron. and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108
Donald L. Wyse
Affiliation:
Dep. of Agron. and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108
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Abstract

Glyphosate transport was studied using the 14C-labeled herbicide. Because glyphosate appears to undergo little metabolism in plants, detected 14C was assumed to indicate the presence of glyphosate. Leaf-girdling experiments demonstrated that 14C-glyphosate [N-(phosphonomethyl)glycine] transport in treated quackgrass [Agropyron repens (L.) Beauv. ♯3 AGRRE] leaves occurred in both leaf symplast and apoplast. Symplastic transport was toward the leaf tip and the leaf base. Apoplastic transport was toward the leaf tip only. Rhizome-girdling experiments showed that translocation of glyphosate from a treated shoot to another shoot on the same rhizome occurs primarily in the rhizome symplast. Girdling the base of quackgrass culms showed that acropetal transport of glyphosate from the rhizome into quackgrass shoots is in the apoplast and the symplast of the culms of quackgrass shoots. Excision of rhizome buds and rhizome apices indicated that the rhizome is a sink for glyphosate independent of rhizome buds or rhizome apices. The concentration of 14C-glyphosate in rhizome buds was less in plants with rhizome apices removed than in those with apices intact. The concentration of C-glyphosate in rhizome apices did not differ between plants with buds removed and those with buds intact. 14C-glyphosate applied to a girdled rhizome apex remained primarily in the apex. Some transport of glyphosate past the girdle occurred, indicating apoplastic transport of glyphosate in the rhizome. Apoplastic transport of 14C-glyphosate in the rhizome was greatest in water-stressed plants.

Keywords

Translocationorgan excisionsource-sink relationshipsAGRRE
Type
Physiology, Chemistry, and Biochemistry
Information
Weed Science , Volume 32 , Issue 6 , November 1984 , pp. 744 - 750
Copyright
Copyright © 1984 by the Weed Science Society of America 

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References

Literature Cited

1. Andersen, R. N. and Koukkari, W. L. 1978. Response of velvetleaf (Abutilon theophrasti) to bentazon as affected by leaf orientation. Weed Sci. 26:393–395.Google Scholar
2. Chase, R. L. and Appleby, A. P. 1979. Effects of humidity and moisture stress on glyphosate control of Cyperus rotundus L. Weed Res. 19:241–246.Google Scholar
3. Claus, J. S. and Behrens, R. 1976. Glyphosate translocation and quackgrass rhizome bud kill. Weed Sci. 24:149–152.Google Scholar
4. Davis, F. S., Merkle, M. G., and Bovey, R. W. 1968. Effect of moisture stress on the absorption and transport of herbicide in woody plants. Bot. Gaz. 129:183–189.Google Scholar
5. Duke, S. H., Koukkari, W. L., and Soulen, T. K. 1975. Glutamate dehydrogenase activity in roots: distribution in a seedling and storage root and the effects of red and far-red illumination. Physiol. Plant. 34:8–13.CrossRefGoogle Scholar
6. Gottrup, O., O'Sullivan, P. A., Schraa, R. J., and Vanden Born, W. H. 1976. Uptake, translocation, metabolism and selectivity of glyphosate in Canada thistle and leafy spurge. Weed Res. 16:197–201.CrossRefGoogle Scholar
7. Jordan, T. N. 1977. Effects of temperature and relative humidity on the toxicity of glyphosate to bermudagrass (Cynodon dactylon). Weed Sci. 25:448–451.Google Scholar
8. Kells, J. J. and Rieck, C. E. 1979. Effects of illuminance and time on the accumulation of glyphosate in johnsongrass (Sorgum halepense). Weed Sci. 28:93–96.Google Scholar
9. Leakey, R. R. B. and Chancellor, R. J. 1975. Parental factors in dominance of lateral buds on rhizomes of Agropyron repens (L.) Beauv. Planta 123:267–274.Google Scholar
10. Marquis, L. Y., Comes, R. D., and Yang, C. P. 1979. Selectivity of glyphosate in creeping red fescue and reed canarygrass. Weed Res. 19:335–342.Google Scholar
11. McIntyre, G. I. 1976. Apical dominance in the rhizome of Agropyron repens: The influence of water stress on bud activity. Can. J. Bot. 54:2747–2754.Google Scholar
12. McWhorter, C. G., Jordan, T. N., and Wills, G. D. 1980. Translocation of 14C-glyphosate in soybeans (Glycine max) and johnsongrass (Sorghum halepense). Weed Sci. 28:113–118.Google Scholar
13. Merkle, M. G. and Davis, F. S. 1967. Effects of moisture stress on absorption and movement of picloram and 2,4,5-T in beans. Weeds 15:10–12.Google Scholar
14. Moosavi-Nia, H. and Dore, J. 1979. Factors affecting glyphosate activity in Imperata cylindrica (L.) Beauv. and Cyperus rotundus L. I. Effect of soil moisture. Weed Res. 15:137–143.CrossRefGoogle Scholar
15. Pallas, J. E. and Williams, G. G. 1962. Foliar absorption and translocation of 32P and 2,4-dichlorophenoxyacetic acid as affected by soil moisture tension. Bot. Gaz. 123:175–180.CrossRefGoogle Scholar
16. Richard, E. P. and Slife, F. W. 1979. In vivo and in vitro characterization of the foliar entry of glyphosate in hemp dogbane (Apocynum cannabinum). Weed Sci. 27:426–433.Google Scholar
17. Scholander, P., Hammel, H. T., and Bradstreet, E. D. 1965. Sap pressure in vascular plants. Science 148:339–346.Google Scholar
18. Sequra, J., Bingham, S. W., and Foy, C. L. 1979. Phytotoxicity of glyphosate to Italian ryegrass (Lolium multiflorum) and red clover (Trifolium pratense). Weed Sci. 26:32–36.Google Scholar
19. Shaner, D. L. and Lyon, J. L. 1980. Interaction of glyphosate with aromatic amino acids on transpiration in Phaseolus vulgaris . Weed Sci. 28:31–35.Google Scholar
20. Sprankle, P., Meggitt, W. F., and Penner, D. 1975. Absorption, action, and translocation of glyphosate. Weed Sci. 23:235–240.Google Scholar
21. Werner, P. A. and Rioux, R. 1977. The biology of Canadian weeds. 24. Agropyron repens (L.) Beauv. Can. J. Plant Sci. 57:905–919.Google Scholar
22. Westra, P. H. and Wyse, D. L. 1981. Growth and development of quackgrass (Agropyron repens) biotypes. Weed Sci. 29:44–52.Google Scholar
23. Whitwell, T., Banks, P., Bassler, E., and Santelmann, P. W. 1980. Glyphosate absorption and translocation in bermudagrass (Cynodon dactylon) and activity in horsenettle (Solanum carolinense). Weed Sci. 28:93–96.Google Scholar
24. Wills, G. D. 1978. Factors affecting toxicity and translocation of glyphosate in cotton (Gossypium hirsutum). Weed Sci. 26:509–513.CrossRefGoogle Scholar
25. Wyril, J. B. and Burnside, O. C. 1976. Absorption, translocation, and metabolism of 2,4-D and glyphosate in common milkweed and hemp dogbane. Weed Sci. 24:557–566.Google Scholar
26. Zandstra, B. H. and Nishimoto, R. K. 1977. Movement and activity of glyphosate in purple nutsedge. Weed Sci. 25:268–271.Google Scholar