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Environmental effects on the induction of wheat chemical defences by aphid infestation

  • Plant Animal Interactions
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Abstract

The effects of temperature and photoperiod on the ability of wheat (Triticum aestivum L.) seedlings to show induced responses (increased accumulation of hydroxamic acids, Hx) upon infestation by the bird cherry-oat aphid, Rhopalosiphum padi L. were evaluated under laboratory conditions. Induction of Hx was significantly higher at lower temperatures. No such clear trend was found for the photoperiod effect. The significant effect of environmental conditions on growth rate of seedlings and the significant negative correlation between growth rate prior to infestation and induction of Hx suggested that environmental effects on induced responses were at least partially mediated through their effect on plant growth rate. After statistically uncoupling the effect of environmental conditions from the effect of plant growth rate, the effect of temperature on induction of Hx was no longer significant. Therefore, the temperature effect was mediated by plant growth rate.

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References

  • Argandoña VH, Niemeyer HM, Corcuera LJ (1981) Effect of content and distribution of hydroxamic acids in wheat on infestation by Schizaphis graminum. Phytochemistry 20: 673–676

    Google Scholar 

  • Baldwin IT, Karb MJ, Ohnmeiss TE (1994) Allocation of 15N from nitrate to nicotine: production and turnover of a damage-induced mobile defense. Ecology 75: 1703–1713

    Google Scholar 

  • Bazzaz FA, Chiariello NR, Coley PD, Pitelka LF (1987) Allocating resources to reproduction and defense. Bioscience 37: 58–67

    Google Scholar 

  • Braga MR, Young MCM, Dietrich SMC, Gottlieb OR (1991) Phytoalexin induction in Rubiaceae. J Chem Ecol 17: 1079–1090

    Google Scholar 

  • Chapin FS, Bloom AJ, Field CB, Waring RH (1987) Plant responses to multiple environmental factors. Bioscience 37: 49–57

    Google Scholar 

  • Coley PD (1988) Effects of plant growth rate and leaf lifetime on the amount and type of anti-herbivore defense. Oecologia 74: 531–536

    Google Scholar 

  • Coley PD, Bryant JP, Chapin FS (1985) Resource availability and plant anti-herbivore defense. Science 230: 895–899

    Google Scholar 

  • Dixon AFG (1985) Aphid ecology. Chapman and Hall, New York

    Google Scholar 

  • Edwards PJ, Wratten SD, Parker EA (1992) The ecological significance of rapid wound-induced changes in plants: insect grazing and plant competition. Oecologia 91: 226–272

    Google Scholar 

  • Givovich A, Niemeyer HM (1995) Comparison of the effect of hydroxamic acids from wheat on five species of cereal aphids. Entomol Exp Appl 74: 115–119

    Google Scholar 

  • Gutiérrez C, Castañera P, Torres V (1988) Would-induced changes in DIMBOA (2,4-dihydroxy-7-methoxy-2H-1,4,3-one) concentration in maize plants by Sesamia nonagrioides Lef. (Lepidoptera, Noctuidae). Ann Appl Biol 113: 447–454

    Google Scholar 

  • Hanhimäki S, Senn J (1992) Sources of variation in rapidly induced responses to leaf damage in the mountain birch-insect herbivore system. Oecologia 91: 318–331

    Google Scholar 

  • Haukioja E, Niemelä P (1979) Birch leaves as a resource for herbivores: seasonal occurrence of increased resistance in foliage after mechanical damage of adjacent leaves. Oecologia 39: 151–159

    Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67: 283–335

    Google Scholar 

  • Jing SW, Coley PD (1990) Dioecy and herbivory: the effect of growth rate on plant defense in Acer negundo. Oikos 58: 369–377

    Google Scholar 

  • Karban R (1987) Environmental conditions affecting the strength of induced resistance: against mites in cotton. Oecologia 73: 414–419

    Google Scholar 

  • Langer RHM (1979) How grasses grow (Studies in Biology 34) Edward Arnold, London

    Google Scholar 

  • Leszczynski B, Dixon AFG (1990) Resistance of cereals to aphids: interaction between hydroxamic acids and the aphid Sitobion avenae (Homoptera: Aphididae). Ann Appl Biol 117: 21–30

    Google Scholar 

  • Neuvonen S, Danell K (1987) Does browsing modify the quality of birch foliage for Epirrita autumnata larvae? Oikos 49: 156–160

    Google Scholar 

  • Nicol D, Copaja SV, Wratten SD, Niemeyer HM (1992) Screen of worldwide wheat cultivars for hydroxamic acids levels and aphid antixenosis. Ann Appl Biol 121: 11–18

    Google Scholar 

  • Niemeyer HM (1988) Hydroxamic acids (4-hydroxy-1,4-benzoxazin-3-ones), defence chemicals in the Gramineae. Phytochemistry 27: 3349–3358

    Google Scholar 

  • Niemeyer HM, Pérez FJ (1995) Potential of hydroxamic acids in the control of cereal pests, diseases and weeds. In: Inderjit Dakshini KMM, Einhellig FA (eds) Allelopathy. Organisms, processes, and applications (Symposium series 582). ACS, Washington, pp 260–269

    Google Scholar 

  • Niemeyer HM, Pesel E, Copaja SV, Bravo HR, Franke S, Francke W (1989) Changes in hydroxamic acids levels of wheat plants induced by aphid feeding. Phytochemistry 28: 447–449

    Google Scholar 

  • Redak RA, Capinera JL (1994) Changes in western wheatgrass foliage quality following defoliation: consequences for a graminivorous grasshopper. Oecologia 100: 80–88

    Google Scholar 

  • Sagers CL, Coley PD (1995) Benefits and costs of defense in a neotropical shrub. Ecology 76: 1835–1843

    Google Scholar 

  • Tallamy DW, Raupp MJ (1991) Phytochemical induction by herbivores. Wiley, New York

    Google Scholar 

  • Thackray DJ, Wratten SD, Edwards PJ, Niemeyer HM (1990) Resistance to the aphids Sitobion avenae and Rhopalosiphum padi in Gramineae in relation to hydroxamic acid levels. Ann Appl Biol 126: 573–582

    Google Scholar 

  • Wallner WE, Walton GS (1979) Host defoliation: a possible determinant of gypsy moth population quality. Ann Entomol Soc Am 72: 62–67

    Google Scholar 

  • Weibull J, Niemeyer HM (1995) Changes in dihydroxymethoxybenzoxazinone glucoside content in wheat plants infected by three plant pathogenic fungi. Physiol Mol Plant Pathol 47: 201–209

    Google Scholar 

  • Wellings PW, Dixon AFG (1987) Sycamore aphid numbers and population density. III. The role of aphid induced change in plant quality. J Anim Ecol 56: 161–170

    Google Scholar 

  • Wolfson JL, Murdoch LL (1990) Growth of Manduca sexta on wounded tomato plants: role of induced proteinase inhibitors. Entomol Exp Appl 54: 257–264

    Google Scholar 

  • Zadoks JC, Chang TT, Consak CF (1974) A decimal code for the growth stage of cereals. Weed Res 14: 415–421

    Google Scholar 

  • Zangerl AR, Bazzaz FA (1992) Theory and pattern in plant defense allocation. In: Fritz RS, Simms EL (eds) Plant resistance to herbivores and pathogens. Ecology, evolution and genetics. University of Chicago Press, Chicago, pp 363–391

    Google Scholar 

  • Zangerl AR, Berembaum MR (1990) Furanocoumarin induction in wild parsnip: genetics and populational variation. Ecology 71: 1933–1940

    Google Scholar 

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Gianoli, E., Niemeyer, H.M. Environmental effects on the induction of wheat chemical defences by aphid infestation. Oecologia 107, 549–552 (1996). https://doi.org/10.1007/BF00333947

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  • DOI: https://doi.org/10.1007/BF00333947

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