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Identification of Volatile Compounds Released by Leaves of the Invasive Plant Croftonweed (Ageratina adenophora, Compositae), and their Inhibition of Rice Seedling Growth

Published online by Cambridge University Press:  20 January 2017

Fengjuan Zhang*
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Jianying Guo
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Fengxin Chen
Affiliation:
College of Life Science, Hebei University, Baoding, Hebei, 071002, China
Wanxue Liu
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
Fanghao Wan*
Affiliation:
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection (South Campus), Chinese Academy of Agricultural Sciences, Beijing, 100081, China
*
Corresponding author's E-mail: [email protected]
Corresponding author's E-mail: [email protected]

Abstract

Several volatile allelochemicals were identified and characterized from fresh leaf tissues of the invasive croftonweed. A simple bioassay was used to demonstrate the release of volatile allelochemicals from leaf tissues. The bioassays revealed that foliar volatile components of croftonweed exhibited significant effects on the seedling growth of upland rice. Peroxidase (POD) activity, superoxide dismutase (SOD) activity, and root oxidizability rose as the concentration of volatiles increased. Activity for both POD and SOD significantly increased with exposure to 15 g and 20 g of croftonweed leaf tissue for 5 d. Root activity was significant at 10 g compared to the control. The volatile components also stimulated the development of the aerenchyma tissue and inhibited lateral root formation. Leaf volatiles of croftonweed were identified by gas chromatography coupled with mass spectrometry (GC–MS). Some of the compounds identified included α-phellandrene, camphene, ρ-cymene, 2-carene, α-pinene, limonene, and (z)-3-hexen-1-ol. Bioassays showed that four of these compounds could account for the observed phytotoxicity imparted by total leaf volatiles. Limonene, 2-carene, α-pinene and camphene had no phytotoxic effect on shoot elongation. Phellandrene did cause inhibition in shoot growth at all concentrations. Both (z)-3-hexene-1-ol and ρ-cymene inhibited both shoot elongation and root elongation, but the effects of the two compounds on root length were more significant than on the shoot length.

Type
Weed Biology and Ecology
Copyright
Copyright © Weed Science Society of America 

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Footnotes

Current address: Professor, College of Life Science, Hebei University, Baoding, Hebei, 071002, China.

References

Literature Cited

Arnon, D. I. 1949. Copper enzymes in isolated chloroplasts, polyphenoloxidase in Beta vulgaris L. Plant Physiol. 24:115.Google Scholar
Barney, J. N., Hay, A. G., and Weston, L. A. 2005. Isolation and characterization of allelopathic volatiles from mugwort (Artemisia vulgaris). J. Chem. Ecol. 31:247265.Google Scholar
Barney, J. N., Sparks, J. P., Greenberg, J., Whitlow, T. H., and Guenther, A. 2009. Biogenic volatile organic compounds from an invasive species: impacts on plant–plant interactions. Plant Ecol. 203:195205.Google Scholar
Baruah, N. C., Sarma, S., and Shara, R. P. 1994. Seed germination and growth inhibitory cadinenes from Eupatorium adenophorum Spreng. J. Chem. Ecol. 20:18851892.Google Scholar
Batish, D. R., Singh, H. P., Setia, N., Kaur, S., and Kohli, R. K. 2006. 2-Benzoxazolinone (BOA) induced oxidative stress, lipid peroxidation and changes in some antioxidant enzyme activities in mung bean (Phaseolus aureus). Plant Physiol. BioChem. 44:819827.Google Scholar
Beauchamp, C. and Fridovich, I. 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal. BioChem. 44:276287.CrossRefGoogle Scholar
Bohlmann, F. and Gupta, R. K. 1981. Six cadinene derivatives from Ageratina adenophora . Phytochemistry. 20:14321433.Google Scholar
Bordoloi, M. J., Shukla, V. S., and Sharma, R. P. 1985. Absolute stereochemistry of the insect antifeedant cadinene from Eupatorium adenophorum . Tetrahedron Lett. 26:509510.Google Scholar
Callaway, R. M. and Aschehoug, E. T. 2000. Invasive plants versus their new and old neighbors: a mechanism for exotic invasion. Science. 290:521523.Google Scholar
Callaway, R. M. and Ridenour, W. M. 2004. Novel weapons: a biochemically based hypothesis for invasive success and the evolution of increased competitive ability. Front. Ecol. Environ. 2:436443.Google Scholar
Cappuccino, N. and Arnason, J. T. 2006. Novel chemistry of invasive exotic plants. Biol. Lett. 2:189193.Google Scholar
Comas, D., Calafell, F., Mateu, E., et al. 1998. Trading genes along the silk road: mtDNA sequences and the origin of central Asian populations. Am. J. Hum. Genet. 63:18241838.Google Scholar
Crawly, M. J. 1987. What makes a community invasible? Pages 429451 in Crawley, M. J. and Edwards, P. J., eds. Colonization, Succession, and Stability. Oxford, United Kingdom Blackwell.Google Scholar
Cronk, Q. C. B. and Fuller, J. L. 1995. Plant invaders: The Threat to Natural Ecosystems. Chapman and Hall. 241 p.Google Scholar
Daehler, C. C. 2003. Performance comparisons of co-occurring native and alien invasive plants: implications for conservation and restoration. Ann. Rev. Ecol. Syst. 34:183211.Google Scholar
Dayan, F. E. and Watson, S. B. 2011. Plant cell membrane as a marker for light-dependent and light-independent herbicide mechanisms of action. Pestic. Biochem. Physiol. 101:182190.Google Scholar
De Moraes, C. M., Lewis, W. J., Pare, P. W., Alborn, H. T., and Tumlinson, J. H. 1998. Herbivore-infested plants selectively attract parasitoids. Nature. 393:570573.Google Scholar
De Moraes, C. M., Mescher, M. C., and Tumlinson, J. H. 2001. Caterpillar-induced nocturnal plant volatiles repel conspecific females. Nature. 410:577580.Google Scholar
Elton, C. S. 1958. The Ecology of Invasions by Animals and Plants. London, UK Methuen. 139 p.Google Scholar
Eom, S. H., Yang, H. S., and Weston, L. A. 2006. An evaluation of the allelopathic potential of selected perennial groundcovers: foliar volatiles of catmint (Nepeta × faassenii) inhibit seedling growth. J. Chem. Ecol. 32:18351848.Google Scholar
Fehsenfeld, F., Calvert, J., Fall, R., et al. 1992. Emissions of volatile organic compounds from vegetation and the implications for atmospheric chemistry. Glob. Biogeochem. Cycles. 6:389430.Google Scholar
Grotkopp, E., Rejmánek, M., and Rost, T. L. 2002. Toward a causal explanation of plant invasiveness: seedling growth and life-history strategies of 29 pine (Pinus) species. Am. Nat. 159:396419.Google Scholar
Guenther, A., Hewitt, C. N., and Erickson, D. 1995. A global model of natural volatile organic compound emission. J. Geophys. Res. 100:88738892.Google Scholar
Hierro, J. L. and Callaway, R. M. 2003. Allelopathy and exotic plant invasion. Plant Soil. 256:2939.Google Scholar
Hiscox, J. D. and Israelstam, G. F. 1979. A method for the extraction of chlorophyll from leaf tissue without maceration. Can. J. Bot. 57:13321334.Google Scholar
Hoballah, M. E. F. and Turlings, T. C. J. 2001. Experimental evidence that plants under caterpillar attack may benefit from attracting parasitoids. Evol. Ecol. Res. 3:553565.Google Scholar
Inderjit, , Callaway, R. M., and Vivanco, J. M. 2006. Can plant biochemistry contribute to understanding of invasion ecology? Trends Plant Sci. 11:574580.Google Scholar
Inderjit, , Evans, H., Crocoll, C., et al. 2011. Volatile chemicals from leaf litter are associated with invasiveness of a neotropical weed in Asia. Ecology. 92:316324.Google Scholar
Jose, S. 2002. Black walnut allelopathy: current state of the science. Pages 149172 in Inderjit, and Mallik, A. U., eds. Chemical Ecology of Plants: Allelopathy in Aquatic and Terrestial Ecosystems. Basel, Switzerland Birkhäuser Verlag.Google Scholar
Kaushal, V., Dawra, R. K., Sharma, O. P., and Kurade, N. P. 2001. Hepatotoxicity in rat induced by partially purified toxins from Eupatorium adenophorum (Ageratina adenophora). Toxicon. 39:615619.Google Scholar
Khaliq, A., Matloob, A., Farooq, M., Mushtaq, M. N., and Khan, M. B. 2011. Effect of crop residues applied isolated or in combination on the germination and seedling growth of horse purslane (Trianthema portulacastrum L.). Planta Daninha. 29:121128.Google Scholar
Kong, C. H., Hu, F., and Xu, X. H. 2002. Allelopathic potential and chemical constituents of volatiles from Ageratum conyzoides under stress. J. Chem. Ecol. 28:11731182.Google Scholar
Màcias, F. A., Molinillo, J. M. G., Galindo, J. C. G., Varela, R. M., Simonet, A. M., and Castellano, D. 2001. The use of allelopathic studies in the search for natural herbicides. Pages 237256 in Kohli, R. K., Singh, H. P., and Batish, D. R., eds. Allelopathy in Agroecosystems. New York Food Products Press an Imprint of the Howarth Press.Google Scholar
Mack, R. N., Simberloff, D., Lonsdale, W. M., Evans, H., Clout, M., and Bazzaz, F. A. 2000. Biotic invasions: causes, epidemiology, global consequences, and control. Ecol. Appl. 10:689710.Google Scholar
Moreno-Alías, I., León, L., Rosa, R., and Rapoport, H. F. 2009. Morphological and anatomical evaluation of adult and juvenile leaves of olive plants. Trees. 23:181187.Google Scholar
Muller, C. H. 1965. Inhibitory terpenes volatilized from Salvia shrubs. Bull. Torrey Bot Club. 92:3845.Google Scholar
Muller, C. H., Muller, W. H., and Haines, B. L. 1964. Volatile growth inhibitors produced by aromatic shrubs. Science. 143:471473.Google Scholar
Nishida, N., Tamotsu, S., Nagata, N., Satto, C., and Sakai, A. 2005. Allelopathic effects of volatile monoterpenoids produced by Salvia leucophylla: inhibition of cell proliferation and DNA synthesis in the root apical meristem of Brassica campestris seedlings. J. Chem. Ecol. 31:11871203.Google Scholar
Oleszek, W. and Stochmal, A. 2002. Triterpene saponins and flavonoids in the seeds of Trifolium species. Phytochemistry. 61:165170.Google Scholar
Peñuelas, J. and Llusià, J. 2004. Plant VOC emissions: making use of the unavoidable. Trends Ecol. Evol. 19:402404.Google Scholar
Prati, D. and Bossdorf, O. 2004. Allelopathic inhibition of germination by Alliaria petiolata (Brassicaceae). Am. J. Bot. 91:285288.Google Scholar
Qiang, S. 1998. The history and status of the study on croften weed (Eupatorium adenophorum Spreng.) a worst worldwide weed. J. Wuhan Botan. Res. 16:366372.Google Scholar
Rejmánek, M. and Richardson, D. M. 1996. What attributes make some plant species more invasive? Ecology. 77:16551661.Google Scholar
Romagni, J. G., Allen, S. N., and Dayan, F. E. 2000. Allelopathic effects of volatile cineoles on two weedy plant species. J. Chem. Ecol. 26:303313.Google Scholar
Schenk, H. J. 2006. Root competition: beyond resource depletion. J. Ecol. 94:725739.Google Scholar
Shen, H. C., Zhou, W. J., Xi, H. F., and Ye, Q. F. 1991. A preliminary study of physiological and yield effects of paclobutrazol on Brassica napus . Acta Agric. Univ. Zhejiang. 17:423426.Google Scholar
Shukla, V. S., Barua, N. C., Chowdhury, P. K., Sharma, R. P., and Bordoloi, M. 1986. Absolute stereochemistry of the cadinenes from Eupatorium adenophorum . Tetrahedron. 42:11571167.Google Scholar
Singh, H. P., Batish, D. R., Kaur, S., Arora, K., and Kohli, R. K. 2006. α-Pinene inhibits growth and induces oxidative stress in roots. Ann. Bot. 98:12611270.Google Scholar
Singh, H. P., Batish, D. R., Kohli, R. K., and Arora, K. 2007. Arsenic-induced root growth inhibition in mung bean (Phaseolus aureus Roxb.) is due to oxidative stress resulting from enhanced lipid peroxidation. Plant Growth Regul. 53:6573.Google Scholar
Song, Q. S., Fu, J., Tang, J. W., Feng, Z. L., and Yang, C. R. 2000. Allelopathic potential of Eupatorium adenophorum Spreng. Acta Phytoecol. Sinica. 24:362365.Google Scholar
Srivalli, B., Sharma, G., and Khanna-Chopra, R. 2003. Antioxidative defence system in an upland rice cultivar subjected to increasing intensity of water stress followed by recovery. Physiol. Plant. 119:503512.Google Scholar
Stachowicz, J. J. and Tilman, D. 2005. Species invasions and the relationships between species diversity, community saturation, and ecosystem functioning. Pages 4164 in Sax, D. F., Stachowicz, J. J., and Gaines, S. D., eds. Species Invasions: Insights into Ecology, Evolution, and Biogeography. Sunderland, MA Sinauer.Google Scholar
Thaler, J. S. 1999. Jasmonate-inducible plant defenses cause increased parasitism of herbivores. Nature. 399:686688.Google Scholar
Tiwari, B. S., Belenghi, B., and Levine, A. 2002. Oxidative stress increased respiration and generation of reactive oxygen species, resulting in ATP depletion, opening of mitochondrial permeability transition, and programmed cell death. Plant Physiol. 128:12711281.Google Scholar
Tripathi, R. S., Singh, R. S., and Pai, J. P. N. 1981. Allelopathic potential of Eupatorium adenophorum, a dominant ruderal weed of Meghalaya. Proc. Indian Natl. Sci. Acad. Part B Biol. Sci. 47:458465.Google Scholar
Turlings, T. C. J., Tumlinson, J. H., and Lewis, W. J. 1990. Exploitation of herbivore-induced plant odors by host-seeking parasitic wasps. Science. 250:12511253.Google Scholar
Weir, T. L., Park, S. W., and Vivanco, J. M. 2004. Biochemical and physiological mechanisms mediated by allelochemicals. Curr. Opin. Plant Biol. 7:472479.Google Scholar
Yang, G. Y., Wan, F. H., and Liu, W. X. 2008. Influences of main-functional allelochemicals derived from the leachates of Ageratina adenophora Sprenge on anatomical structures of upland rice seedling root tips. Plant Protec. 34:2024.Google Scholar
Yang, G. Y., Wan, G. H., Liu, W. X., and Zhang, X. W. 2006. Physiological effects of allelochemicals from leachates of Ageratina adenophora (Sprenge) on rice seedlings. J. Allelopathy. 18:237246.Google Scholar
Yu, X. J., Yu, D., Lu, Z. J., and Ma, K. P. 2005. A new mechanism of invader success: exotic plant inhibits natural vegetation restoration by changing soil microbe community. Chinese Sci. Bull. 50:11051112.Google Scholar