Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-22T19:40:35.320Z Has data issue: false hasContentIssue false

Disappearance of DIBOA-glucoside, DIBOA, and BOA from Rye (Secale cereale L.) Cover Crop Residue

Published online by Cambridge University Press:  12 June 2017

Joseph P. Yenish
Affiliation:
Dep. Crop Sci., and Dep. of Bot., N.C. State Univ., Raleigh, NC 27695
A. Douglas Worsham
Affiliation:
Dep. Crop Sci., and Dep. of Bot., N.C. State Univ., Raleigh, NC 27695
W. Scott Chilton
Affiliation:
Dep. Crop Sci., and Dep. of Bot., N.C. State Univ., Raleigh, NC 27695

Abstract

Disappearance of rye cover crop residue and allelochemicals from rye residue were evaluated in a field study at Clayton, NC, in 1992 and 1993. The aerial portion of rye biomass declined linearly over time with 50% of the residue disappearing by 105 d after clipping. Extrapolations indicated all residue would disappear approximately 200 d after rye clipping. Total content of DIBOA and two related compounds, DIBOA-glucoside and BOA, in the residue also was measured over time. Fifty percent of the 0-d content of the compounds disappeared from residue 10 and 12 d after kill for 1992 and 1993, respectively. Extrapolations indicated content reached 0121 and 168 d after kill for 1992 and 1993, respectively. Reported duration of weed suppression by rye cover crops more closely follows disappearance of allelochemicals from rye residue than disappearance of the residue.

Type
Physiology, Chemistry, and Biochemistry
Copyright
Copyright © 1995 by the 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. Atkinson, J., Morand, P., Arason, J. T., Niemeyer, H. M., and Bravo, H. R. 1991. Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one: decomposition to benzoxazolinones and reaction with β-mercaptoethanol. J. Org. Chem. 56:17881800.Google Scholar
2. Barnes, J. P. and Putnam, A. R. 1986. Evidence for allelopathy by residues and aqueous extracts of rye. Weed Sci. 34:384390.Google Scholar
3. Barnes, J. P. and Putnam, A. R. 1987. Role of benzoxazinones in allelopathy by rye. J. Chem. Ecol. 4:889906.CrossRefGoogle Scholar
4. Barnes, J. P., Putnam, A. R., Burke, B. A., and Aasen, A. J. 1986. Isolation and characterization of allelochemicals in rye herbage. Phytochem. 26:13851390.Google Scholar
5. Baskin, J. M. and Baskin, C. C. 1989. Physiology of dormancy and germination in relation to seed bank ecology. Pages 5366 in Leck, M. A., Parker, V. T., and Simpson, R. L., eds. Ecology of Soil Seed Banks. Academic Press, New York.Google Scholar
6. Bredenberg, J. B., Honkanen, E., and Virtanen, A. I. 1962. The kinetics and mechanism of the decomposition of 2,4-dihydroxy-1,4-benzoxazin-3-one. Acta Chem. Scand. 16:135141.CrossRefGoogle Scholar
7. Chase, W. R., Nair, M. G., and Putnam, A. R. 1991. 2,2′-oxo-1,1′-azobenzene: selective toxicity of rye allelochemicals to weed and crop species: II. J. Chem. Ecol. 17:919.Google Scholar
8. Chou, C. H. and Patrick, Z. A. 1976. Identification and phytotoxic activity of compounds produced during decomposition of corn and rye residues in soil. J. Chem. Ecol. 2:369387.Google Scholar
9. Gagliardo, R. W. and Chilton, W. S. 1992. Soil transformation of 2(3H)-benzoxazolone of rye into phytotoxic 2-amino-3H-phenoxazin-3-one. J. Chem. Ecol. 18:16831691.Google Scholar
10. Hofman, J. and Hofmanova, O. 1969. 1,4-benzoxazine derivatives in plants. Sephadex fractionation and identification of a new glucoside. European J. Biochem. 8:109112.CrossRefGoogle Scholar
11. Lehman, M. E. 1993. Effect of allelopathy on plant emergence and growth as modified by physical factors and root distribution. M.S. Thesis, N.C. State Univ. 96 pp.Google Scholar
12. Nair, M. G., Whitenack, C. J., and Putnam, A. R. 1990. 2,2′-oxo-1,1′-azobenzene, a microbially transformed allelochemical from 2,3-benzoxazolinone: I. J. Chem. Ecol. 16:353364.CrossRefGoogle Scholar
13. Niemeyer, H. M. 1988. Hydroxamic acids, defence chemicals in the Gramineae. Phytochem. 27:33493358.CrossRefGoogle Scholar
14. Putnam, A. R. 1988. Allelochemicals from plants as herbicides. Weed Technol. 2:510518.Google Scholar
15. Shilling, D. G., Jones, L. A., Worsham, A. D., Parker, C. E., and Wilson, R. F. 1986. Isolation and identification of some phytotoxic compounds from aqueous extracts of rye. J. Agric. Food Chem. 34:633638.Google Scholar
16. Tipton, C. L., Wang, M. C., Tsao, F.H.C., Tu, C.C.L., and Husted, R. R. 1973. Biosynthesis of 1,4-benzoxazin-3-ones in Zea mays . Phytochem. 12:347352.Google Scholar
17. Virtanen, A. I. and Hietala, P. K. 1960. Precursers of benzoxazolinone in rye plants I. Precursor II, the aglycone. Acta Chem. Scand. 14:499502.Google Scholar
18. Wolf, R. B., Spencer, G. F., and Plattner, R. D. 1985. Benzoxazolinone, 2-4-dihydroxy-1,4-benzoxazin-3-one, and its glucoside from Acanthus mollis seeds inhibit velvetleaf germination and growth. J. Nat. Prod. 48:5963.CrossRefGoogle Scholar
19. Woodward, M. D., Corcuera, L. J., Helgeson, J. P., and Upper, C. D. 1978. Decomposition of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one in aqueous solutions. Plant Physiol. 61:796802.Google Scholar
20. Worsham, A. D. 1989. Current and potential techniques using allelopathy as an aid in weed management. Pages 275291 in Chou, C. H. and Waller, G. R., eds. Phytochemical Ecology: Allelochemicals, Mycotoxins and Insect Pheromones. Inst. of Botany, Academia Sinica Monograph Ser. No. 9, Taipei, ROC.Google Scholar
21. Worsham, A. D. and Blum, U. 1992. Allelopathic cover crops to reduce herbicide inputs in cropping systems. Proc. of the First Int. Weed Cont. Cong. 2:577579.Google Scholar
22. Zuniga, G. E., Argandona, V. H., Niemeyer, H. M., and Corcuera, L. J. 1983. Hydroxamic acid content in wild and cultivated Gramineae. Phytochem. 22:26652668.Google Scholar