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2016 | 56 | 1 |

Tytuł artykułu

Effect of epicuticular waxes from triticale on the feeding behaviour and mortality of the grain aphid, Sitobion avenae (Fabricius) (Hemiptera: Aphididae)

Autorzy

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Surface waxes from wax-covered triticale plants (RAH 122) were sprayed on plants of the waxless genotype RAH 366 or the surface waxes were used to make artificial diet preparations. The results were significant increases in the mortality of apterous adults of the grain aphid Sitobion avenae (Fabricius) (Hemiptera: Aphididae) at all concentrations tested in comparison with those aphids which fed on the control plants or aphids which were reared on the diets. In the choice tests, most aphids settled on plants without surface waxes or on diet preparations which did not have surface waxes (the controls). When the concentration of the surface waxes was increased on one of the plants or surface waxes were increased in the diet preparation, the number of wandering aphids increased. Those aphids which did not wander were mainly on the waxless control plants or on the waxless diet preparations. Aphids did settle on those plants or on the diet preparations which had 100 and 1,000 μg · g–1 of surface wax. The aphids rarely settled on the diet preparations containing 10,000 μg ∙ g–1 of surface waxes. From these observations it appears that surface waxes can act as a feeding deterrent. Since aphids on plants with surface waxes, or aphids which settled on diet preparations with surface waxes, started to die earlier than aphids fed only the control plants or the control diet preparations, it is possible that the surface waxes had a toxic effect that led to early mortality. Thus, it can be said that the surface waxes caused feeding deterrence and had a toxic effect on the aphids.

Wydawca

-

Rocznik

Tom

56

Numer

1

Opis fizyczny

p.39-44,fig.,ref.

Twórcy

autor
  • Department of Biochemistry and Molecular Biology, Institute of Biology, University of Natural Sciences and Humanities in Siedlce, 12B Prusa St., 08-110 Siedlce, Poland

Bibliografia

  • Athukorala Y., Mazza G. 2010. Supercritical carbon dioxide and hexane extraction of wax from triticale straw: content, composition and thermal properties. Industrial Crops and Products 31 (3): 550–556.
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  • Buschhaus C., Jetter R. 2011. Composition differences between epicuticular and intracuticular wax substructures: How do plants seal their epidermal surfaces? Journal of Experimental Botany 62 (3): 841–853.
  • Eigenbrode S.D., Espelie K.E. 1995. Effects of plant epicuticular lipids on insect herbivores. Annual Review of Entomology 40: 171–194.
  • Eigenbrode S.D., Kabalo N.N., Rutledge C.A. 2000. Potential of reduced-waxbloom oilseed Brassica for insect pest resistance. Journal of Agricultural and Urban Entomology 17 (2): 53–63.
  • Espelie K.E., Bernays E.A., Brown J.J. 1991. Plant and insect cuticular lipids serve as behavioral cues for insects. Archives of Insect Biochemistry and Physiology 17 (4): 223–233.
  • Haliński Ł.P., Paszkiewicz M., Gołębiowski M., Stepnowski P. 2012. The chemical composition of cuticular waxes from leaves of the gboma eggplant (Solanum macrocarpon L.). Journal of Food Composition and Analysis 25 (1): 74–78.
  • Ji X., Jetter R. 2008. Very long chain alkylresorcinols accumulate in the intracuticular wax of rye (Secale cereale L.) leaves near the tissue surface. Phytochemistry 69 (5): 1197–1207.
  • Ni X., Quisenberry S.S., Siegfried B.D., Lee K.W. 1998. Influence of cereal leaf epicuticular wax on Diuraphis noxia probing behavior and nymphosition. Entomologia Experimentalis et Applicata 89: 111–118.
  • Powell G., Maniar S.P., Pickett J.A., Hardie J. 1999. Aphid responses to non-host epicuticular lipids. Entomologia Experimentalis et Applicata 91 (1): 115–123.
  • Razeq F.M., Kosma D.K., Rowland O., Molina I. 2014. Extracellular lipids of Camelina sativa: Characterization of chloroform-extractable waxes from aerial and subterranean surfaces. Phytochemistry 106 (1): 188–196.
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  • Sas-Piotrowska B., Piotrowski W., Kaczmarek-Cichosz R. 2005. In the last years research on possibility to make use of natura biologically active substances. Journal of Plant Protection Research 45 (3): 181–193
  • Sarkar N., Mukherjee A., Barik A. 2013. Long-chain alkanes: allelochemicals for host location by the insect pest, Epilachna dodecastigma (Coleoptera: Coccinellidae). Applied Entomology and Zoology 48 (2): 171–179.
  • Städler E., Reifenrath K. 2009. Glucosinolates on the leaf surface perceived by insect herbivores: review of ambiguous results and new investigations. Phytochemistry Reviews 8 (1): 207–225.
  • Steinbauer M.J., Matsuki M. 2004. Suitability of Eucalyptus and Corymbia for Mnesampela private (Guenée) (Lepidoptera: Geometridae) larvae. Agricultural For Entomology 6 (4): 323–332.
  • Steinbauer M.J., Schiestl F.P., Davies N.W. 2004. Monoterpenes and epicuticular waxes help female autumn gum moth differentiate between waxy and glossy Eucalyptus and leaves of different ages. Journal of Chemical Ecology 30 (6): 1117–1142.
  • Supapvanich S., Pimsaga J., Srisujan P. 2011. Physicochemical changes in fresh-cut wax apple (Syzygium samarangenese [Blume] Merrill & L. M. Perry) during storage. Food Chemistry 127 (3): 912–917.

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Bibliografia

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