Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-25T00:43:07.186Z Has data issue: false hasContentIssue false

Allelopathic Potential of Hope White Lupine (Lupinus albus) Herbage and Herbage Extracts

Published online by Cambridge University Press:  12 June 2017

Fredric R. Lehle
Affiliation:
Dep. Agron., Univ. of Arkansas, Fayetteville, AR 72701
Robert Frans
Affiliation:
Dep. Agron., Univ. of Arkansas, Fayetteville, AR 72701
Marilyn McClelland
Affiliation:
Dep. Agron., Univ. of Arkansas, Fayetteville, AR 72701

Abstract

The allelopathic potentials of Hope white lupine (Lupinus albus L.) herbage and herbage extracts were evaluated. The emergence and growth of cotton (Gossypium hirsutum L. ‘Deltapine 45A’), soybean [Glycine max (L.) Merr. ‘Lee 68′], and six weed species under greenhouse conditions were measured after seeding directly into a moist, silt loam soil into which dry Hope lupine herbage, collected at second bloom, had been incorporated at rates from 500 to 8000 ppm (dry herbage/dry soil, w/w). At the lower rates, incorporated Hope white lupine stimulated the emergence of large crabgrass [Digitaria sanguinalis (L.) Scop.]; at the higher rates, cotton emergence was inhibited. Cotton and soybean fresh weights were stimulated at incorporation rates up to 2000 ppm, but were inhibited at higher concentrations. The growth of johnsongrass [Sorghum halepense (L.) Pers.] and large crabgrass was stimulated at most incorporation rates. Stimulated plants were chlorotic and had longer internodes. Emergence and growth of other species tested were not significantly affected by incorporated Hope white lupine. Equivalent concentrations of Hope white lupine herbage extracts were about 17 times more inhibitory to germination of cress (Lepidium sativum L. ‘Curlycress’) seed than to growth of sorghum [Sorghum bicolor (L.) Moench ‘AKS 663′] coleoptiles or radicles. The inhibitory principle extracted from Hope white lupine herbage was non-volatile, heat insensitive, and significantly less active in soil. Fractionation of a herbage extract suggested that neither the alkaloid nor phenolic acid content could account for herbage phytotoxicity in soil.

Type
Research Article
Copyright
Copyright © 1983 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. Birecka, H. 1963. Investigations on alkaloid synthesis in bitter white lupine. Acta Soc. Bot. Pol. 32:131158. (in Polish).CrossRefGoogle Scholar
2. Birecka, H. and Wojcieska, U. 1962. Changes of alkaloid content in plants of Lupinus albus during their vegetation. III. White bitter lupine in the earliest and the last ontogenetic stages. Acta Soc. Bot. Pol. 31:337356. (in Polish).CrossRefGoogle Scholar
3. Davis, L. S. 1897. Lupanine of white lupine. Arch. Pharm. (Weinheim, Ger.) 235:199217. (in German).CrossRefGoogle Scholar
4. Gladstones, J. S. 1970. Lupins as crop plants. Field Crop Abstr. 23:123148.Google Scholar
5. Gonchar, A. I. 1961. Growing row crops with lupine on eroded soils. Zemledelie 5:5053. (in Russian).Google Scholar
6. Guenzi, W. D. and McCalla, T. M. 1966. Phenolic acids in oats, wheat, sorghum, and corn residues and their phytotoxicity. Agron. J. 58:303304.CrossRefGoogle Scholar
7. Harborne, J. B., Boulter, D., and Turner, B. L., eds. 1971. Chemotaxonomy of the Leguminosae. Academic Press, London. 612.Google Scholar
8. Lehle, F. R. and Putnam, A. R. 1982. Quantification of allelopathic potential of sorghum residues by novel indexing of Richards' function fitted to cumulative cress seed germination curves. Plant Physiol. 69:12121216.CrossRefGoogle ScholarPubMed
9. Macek, K. 1963. Detection reagents-D. Pages 781827 in Hais, I. M. and Macek, K., eds. Paper Chromatography: A Comprehensive Treatise. Publ. House Czech. Acad. Sci., Prague.Google Scholar
10. Mann, H. H. 1958. Field studies in green manuring. Empire J. Exp. Agric. 26:274282.Google Scholar
11. McKee, R. 1947. Lupines: new legumes for the South. U.S. Dep. Agric. Farmers Bull. 1946. U.S. Gov. Printing Off., Washington, DC. 10.Google Scholar
12. Miyaska, S., Inforzato, R., Mascarenhas, H.A.A., and Kiihl, R.A.S. 1967. Elongation of the bean plant stem stimulated by the incorporation in the soil of vegetal matter of lupine plants (Lupinus albus L.). Bragantia 26:2734. (in Portuguese).Google Scholar
13. Offutt, M. S. 1971. Registration of Hope white lupine. Crop Sci. 11:602.CrossRefGoogle Scholar
14. Prochazka, K. 1963. Cyclic acids. Pages 354360 in Hais, I. M. and Macek, K., eds. Paper Chromatography: A Comprehensive Treatise. Publ. House Czech. Acad. Sci., Prague.Google Scholar
15. Putnam, A. R. and Duke, W. B. 1978. Allelopathy in agroecosystems. Annu. Rev. Phytopathol. 16:431451.CrossRefGoogle Scholar
16. Tang, C. and Young, C. 1982. Collection and identification of allelopathic compounds from the undisturbed root system of Bigalta limpograss (Hemartbria altissima). Plant Physiol. 69:155160.CrossRefGoogle ScholarPubMed
17. Zweig, G. and Sherma, J. 1972. Detection reagents for paper and/or thin-layer chromatography. Pages 105189 in Zweig, G. and Sherma, J., ed. CRC Handbook of Chromatography, Vol. II. CRC Press, Cleveland, OH.Google Scholar