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Evidence for allelopathic interference of Japanese honeysuckle (Lonicera japonica) to loblolly and shortleaf pine regeneration

Published online by Cambridge University Press:  20 January 2017

B. W. Skulman ,
J. D. Mattice ,
M. D. Cain  and
E. E. Gbur
J. D. Mattice
Affiliation:
Department of Crop, Soil, and Environmental Sciences, University of Arkansas, 1366 West Altheimer Drive, Fayetteville, AR 72704
M. D. Cain
Affiliation:
USDA Forest Service, Southern Research Station, Forest Resources Building, University of Arkansas at Monticello, P.O. Box 3516, Monticello, AR 71656-3516
E. E. Gbur
Affiliation:
Agricultural Statistics Lab, AGRX-101, University of Arkansas, Fayetteville, AR 72701
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Abstract

Japanese honeysuckle presents a serious problem to the economically attractive natural regeneration of loblolly and shortleaf pine. This research investigated the potential allelopathic interference mechanisms of Japanese honeysuckle in relation to pine regeneration and growth, which may provide insight into overcoming this problem. The allelopathic potential of root exudates and leaf litter from Japanese honeysuckle was tested against loblolly and shortleaf pine seedlings. When Japanese honeysuckle and loblolly pine seedlings were grown using the same irrigation reservoir, there was no significant effect on the growth of either pine species. Exudates of Japanese honeysuckle grown as a pure culture in donor cups also produced no growth effects on pure-cultured pine seedlings grown in acceptor cups. In other assays, aqueous extracts of Japanese honeysuckle leaf tissue were toxic to duckweeds at concentrations well below levels where plasmolysis might cause effects. When Japanese honeysuckle leaf tissue was added to soil at a rate of 2 g tissue 100 g−1 soil, mean seedling height at 128 d after planting was reduced by as much as 40%. Moreover, pine seedlings grown in the presence of Japanese honeysuckle tissue exhibited significant chlorosis of the shoot and needles. Gas chromatography–mass spectroscopy analyses and high-performance liquid chromatography of Japanese honeysuckle leaf tissue aqueous extracts confirmed the presence of five compounds previously identified as possible allelochemicals: 4-hydroxycinnamic acid; 2-hydroxycinnamic acid; 3,4-dihydroxybenzoic acid; 3,4-dihydroxycinnamic acid; and chlorogenic acid. Results indicate that allelopathy plays at least a partial role in Japanese honeysuckle interference with loblolly and shortleaf pine.

Keywords

Japanese honeysuckle, Lonicera japonica Thunb.loblolly pine, Pinus taeda L.shortleaf pine, Pinus echinata Millduckweed, Lemna minor L.AllelopathygerminationLonicera japonicaPinus taedaPinus echinatainterference
Type
Weed Management
Information
Weed Science , Volume 52 , Issue 3 , June 2004 , pp. 433 - 439
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Cain, M. D. 1985. Japanese Honeysuckle and Associated Groundcover Inhibit Establishment and Growth of Pine Seedlings in All-aged Stands. New Orleans, LA: Southern Forest Experiment Station Gen. Tech. Rep. SO-54. Pp. 300–304.Google Scholar
Cain, M. D. 1991. Hardwoods on pine sites: competition or antagonistic symbiosis. For. Ecol. Manag 44:147–160.CrossRefGoogle Scholar
Cain, M. D. 1992. Japanese honeysuckle in uneven-aged pine stands: problems with natural regeneration. Proc. South. Weed Sci. Soc 45:264–269.Google Scholar
Drost, D. C. and Doll, J. D. 1980. The allelopathic effect of yellow nutsedge (Cyperus esculentus) on corn (Zea mays) and soybeans (Glycine max). Weed Sci 28:229–233.CrossRefGoogle Scholar
Einhellig, F. A., Leather, G. R., and Hobbs, L. L. 1985. Use of Lemna minor as a bioassay in allelopathy. J. Chem. Ecol 2:65–72.CrossRefGoogle Scholar
Jain, R., Singh, M., and Dezman, D. J. 1989. Qualitative and quantitative characterization of phenolic compounds from Lantana (Latana camara) leaves. Weed Sci 37:302–307.Google Scholar
Leather, G. R. and Einhellig, F. A. 1986. Bioassays in the study of allelopathy. Pages 133–145 in Putnam, A. and Tang, C. eds. The Science of Allelopathy. New York: J. Wiley.Google Scholar
Leatherman, A. D. 1955. Ecological Life-history of Lonicera Japonica Thunb. . University of Tennessee, Knoxville, TN. 97 p.Google Scholar
Muller, C. H. 1969. Allelopathy as a factor in ecological process. Vegetation 18:348–357.Google Scholar
Rice, E. L. 1974. Allelopathy. New York: Academic. 353 p.Google Scholar
Siccama, T. G., Weir, G., and Wallace, K. 1976. Ice damage in a mixed hardwood forest in Connecticut in relation to Vitus infestation. Bull. Torrey Bot. Club 103:180–183.CrossRefGoogle Scholar
Slezak, W. F. 1976. Lonicera japonica Thunb., an Aggressive Introduced Species in a Mature Forest Ecosystem. . Rutgers University, New Brunswick, NJ. 81 p.Google Scholar
Wigham, D. 1984. The influence of vines on the growth of Liquidambar styraciflua L. (Sweetgum). Can. J. For. Res 14:37–39.Google Scholar