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Effects of Glyphosate on Chloroplast Ultrastructure of Quackgrass Mesophyll Cells

Published online by Cambridge University Press:  12 June 2017

W. F. Campbell
Affiliation:
Utah State Univ., Logan, UT 84322
J. O. Evans
Affiliation:
Utah State Univ., Logan, UT 84322
S. C. Reed
Affiliation:
Utah State Univ., Logan, UT 84322

Abstract

Phytotoxicity of glyphosate (N-(phosphonomethyl) glycine), applied at 0, 0.56, 1.12, 1.68, 2.24 and 4.49 kg ai/ha to uniform, naturally growing quackgrass, [Agropyron repens (L.) Beauv.] plants, was studied with the electron microscope. Visible damage (yellowing of the leaves) to the plants was observed at the 2.24 and 4.49 kg ai/ha dosage rates within 72 hr. Similar damage became evident 120 hr after treatment at the 0.56 to 1.68 dosages. Leaf discs (1 mm in diameter) were harvested at 24, 48, 96, and 192 hr and prepared for electron microscopy by standard techniques. Cellular damage could be detected at all dosage rates as early as 24 hr after treatment. The type of damage observed was partial to complete disruption of the chloroplast envelope, and swelling of the rough endoplasmic reticulum (RER) with a subsequent formation of vesicles. With loss of integrity of the envelope, the chloroplast became completely disrupted with increased time. Other organelles within the cell were also destroyed.

Type
Research Article
Copyright
Copyright © 1976 by the Weed Science Society of America 

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References

Literature Cited

1. Anderson, J.L. and Thomson, W.W. 1973. The effects of herbicides on the ultrastructure of plant cells. Residue Rev. 47:167189.CrossRefGoogle ScholarPubMed
2. Butler, R.D. and Simon, W.W. 1971. Ultrastructural aspects of senescence in plants. Adv. Gerontol. Res. 3:73129.Google Scholar
3. Campbell, W.F. and Evans, J.O. 1970. A rapid method for obtaining leaf samples for electron microscopy. J. Hort. Sci. 5:20.Google Scholar
4. Campbell, W.F. and Evans, J.O. 1971. Influence of some new triazine herbicides on wheat and alfalfa chloroplasts ultrastructure. Abstr. Weed Sci. Soc. Amer. p. 53.Google Scholar
5. Karnovsky, M.J. 1965. A formaldehyde:glutaraldehyde fixative of high osmolarity for use in electron microscopy. J. Cell Biol. 27:137A138A.Google Scholar
6. Mollenhauer, H.H., Whaley, W.G., and Leech, J.H. 1960. Cell ultrastructure responses to mechanical injury. A preliminary report. J. Ultrastruct. Res. 4:473481.CrossRefGoogle ScholarPubMed
7. Reynolds, E.S. 1963. The use of lead citrate at high pH as an electron osmolarity for use in electron microscopy. J. Cell Biol. 17:208212.CrossRefGoogle Scholar
8. Spurr, A.R. 1969. A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26:3143.CrossRefGoogle ScholarPubMed
9. Watson, M.L. 1958. Staining of tissue sections for electron microscopy with heavy metals. J. Biophys. Biochem. Cytol. 4:475478.CrossRefGoogle ScholarPubMed
10. Zucker, M. and Stinson, H.T. 1962. Chloroplasts as the major protein-bearing structures in Oenothera leaves. Arch. Biochem. Biophys. 96:637644.CrossRefGoogle Scholar