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2016 | 25 | 2 |

Tytuł artykułu

Fecundity and survival of grain aphid at various growth stages of waxy and waxless triticale

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Plants use many strategies to protect themselves against insects. Morphological, anatomical, and chemical plant properties play an important role in natural plant resistance to herbivore insects. The effects of triticale genotypes with different wax covers at various growth stages was studied on the fecundity and survival of the grain aphid Sitobion avenae (Fabricius) (Hemiptera: Aphididae). The aphids that fed on the organs of the waxless genotypes survived longer and produced signifi cantly more nymphs. Furthermore, mortality of nymphs on the waxy plants was significantly higher than on waxless plants. The chemical analysis also showed that the waxless plants had lower levels of flavonoids in comparison with waxy plants. Waxless seedlings had lower levels of flavonoids at every studied organ. The obtained results indicate that the level of flavonoids might play an important role in the resistance of winter triticale genotypes to grain aphid. The content of flavonoids was associated with the values of resistance between the waxy and waxless plants. It was concluded that the waxy plants that contained high levels of flavonoids were less preferred by the grain aphid.ces, which indicated no signifi cant change in either periphyton or macrozoobenthos following such episodes.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

25

Numer

2

Opis fizyczny

p.843-849,fig.,ref.

Twórcy

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

Bibliografia

  • 1. SHEPHERD T., ROBERTSON G.W., GRIFFITHS D.W., BIRCH A.N.E. Epicuticular wax ester and triacyloglycerol composition in relation to aphid infestation and resistance in red raspberry (Rubus idaeus L.). Phytochemistry 52, 1255, 1999.
  • 2. BONNEMAIN J.L. Aphids as biological models and agricultural pests. C.R. Biologies 333, 461, 2010.
  • 3. WÓJCICKA A. Importance of epicuticular wax cover for plant/insect interactions: experiment with cereal aphids. Pol. J. Ecol. 61 (1), 183, 2013.
  • 4. WÓJCICKA A. Changes in pigment content of triticale genotypes infested with grain aphid Sitobion avenae (Fabricius) (Homoptera: Aphididae). Acta Biol. Cracov. 56 (1), 121, 2014.
  • 5. WÓJCICKA A. Surface waxes as a plant defense barrier towards grain aphid. Acta Biol. Cracov. 57 (1), DOI: 10.1515/abcsb-2015-0012, 2015.
  • 6. STÄDLER E., REIFENRATH K. Glucosinolates on the leaf surface perceived by insect herbivores: review of ambiguous results and new investigations. Phytochem Rev. 8, 207, 2009.
  • 7. HILKER M., MEINERS T. Plants and insect eggs: How do they affect each other? Phytochemistry 72, 1612, 2011.
  • 8. EIGENBRODE S.D., ESPELIE K.E. Effects of plant epicuticular lipids on insect herbivores. Ann. Rev. Entomol. 40, 171, 1995.
  • 9. NIEMIETZ A., WANDELT K., BARTHLOTT W., KOCH K. Thermal evaporation of multi - component waxes and thermally activated formation of nanotubules for superhydrophobic surfaces. Prog. Org. Coat. 66, 221, 2009.
  • 10. ATHUKORALA Y., MAZZA G. Supercritical carbon dioxide and hexane extraction of wax from triticale straw: Content, composition and thermal properties. Ind. Crop Prod. 31, 550, 2010.
  • 11. YIN Y., BI Y., CHEN S., LI Y., WANG Y., GE Y., DING B., LI Y., ZHANG Z. Chemical composition and antifungal activity of cuticular wax isolated from Asian pear fruit (cv. Pingguoli). Sci. Hort. 129, 577, 2011.
  • 12. HALIŃSKI Ł.P., PASZKIEWICZ M., GOŁĘBIOWSKI M., STEPNOWSKI P. The chemical composition of cuticular waxes from leaves of the gboma eggplant (Solanum macrocarpon L.). J. Food Comp. Anal. 25, 74, 2012.
  • 13. SCHOONHOVEN L.M., VAN LOON J.J.A., DICKE M. Plant Chemistry: Endless Variety. Insect-Plant Biology - Oxford University Press, Chap. 4, Chapman and Hall, London UK, pp. 49-86, 2005.
  • 14. JI X., JETTER R. Very long chain alkylresorcinols accumulate in the intracuticular wax of rye (Secale cereale L.) leaves near the tissue surface. Phytochemistry 69, 1197, 2008.
  • 15. FERNÁNDEZ V., KHAGET M., MONTERO-PRADO P., HEREDIA-GUERRERO J., LIAKOPOULOS G. KAR-ABOURNIOTIS G., DEL RIO V., DOMINGEZ E., TEC-CHINI I., NERIN C., VAL J., HEREDIA A. New inisghts into the properties of pubescent surfaces the peach fruit (Prunus persica L.) as a model. Plant Physiol. 156, 2098, 2011.
  • 16. SUPAPVANICH S., PIMSAGA J., SRISUJAN P. Physico-chemical changes in fresh-cut wax apple (Syzygium sama-rangenese [Blume] Merrill & L. M. Perry) during storage. Food Chem. 127, 912, 2011.
  • 17. BACH L., FAURE J-D. Role of very-long-chain fatty acids in plant development, when chain length does matter. C. R. Biol. 333, 361, 2010.
  • 18. ROSTÁS M., RUF D., ZABKA V. Plant surface wax affects parasitoid's response to host footprints. Naturwissenschaften 95, 997, 2008.
  • 19. AGATI G., TATTINI M. Multiple functional roles of flavonoids in photoprotection. New Phytologist 186, 786, 2010.
  • 20. POLLETIER Y., GIGUÉRE M.A. Effect of manipulations on the host selection behavior of Sitobion avenae (Homoptera : Aphididae). J. Insect Behav. 22, 165, 2009.
  • 21. NAM K.J., HARDIE J. Host acceptance by aphids: Probing and larviposition behaviour of the bird cherry-oat, Rhopalosiphum padi on host and non-host plants. J. Insect Physiol. 58, 660, 2012.
  • 22. TOTTMAN D.R., BROAD H. The decimal code for the growth stages of cereals, with illustrations. Ann. Appl. Biol., 93, 221, 1987.
  • 23. APOBLAZA H.J.V., ROBINSON A.G. Effect of three species of grain aphids (Homoptera: Aphididae) reared on wheat, oats or barley and transferred as adult to wheat, oats and barley. Entomol. Exp. Appl. 10, 358, 1967.
  • 24. KREFT S., ŠTRUKELJ B., GABERŠČIK A., KREFT I. Rutin in buckwheat herbs grown at different UV-B radiation levels: comparison of two UV spectrophotometric and an HPLC method. J. Exp. Botany, 53 (375), 1801, 2002.
  • 25. GORB E. V., VOIGT D., EIGENBRODE S.D., GORB S. Attachment force of the beetle Cryptolaemus montrouzieri (Coleoptera, Coccinellidae) on leaflet surfaces of mutants of the pea Pisum sativum (Fabaceae) with regular and reduced wax coverage. Arthr. Plant Interact. 2, 247, 2008.
  • 26. OU S., ZHAO J., WANG Y., TIAN Y., WANG J. Preparation of octacosanol from filter mud produced after sugarcane juice clarification. LWT - Food Sci. Tech. 45, 295, 2012.
  • 27. PRÜM B., SEIDEL R., BOHN H.F., SPECK T. Plant surface with cuticular folds are slippery for beetles. J. Royal Soc. 9 (6), 127, 2012.
  • 28. MUKHTAR A., DAMEROW L., BLANKE M. Non-invasive assessment of glossiness and polishing of the wax bloom of European plum. Post. Biol. Technol. 87, 144, 2014.
  • 29. MARKSTÄDTER C., FEDERLE W., JETTER R., RIE-DERER M., HÖLLDOBLER B. Chemical composition of the slippery epicuticular wax blooms on Macaranga (Eu-phorbiaceae) ant-plant. Chemoecology 10, 33, 2000.
  • 30. EIGENBRODE S.D., KABALO N.N., RUTLEDGE C.A. Potential of reduced waxbloom oilseed brassica for insect pest resistance. J. Agric. Urban Entomol. 17, 53, 2000.
  • 31. ULRICHS CH., MEWIS I., ADHIKARY S., BHATTACHA-RYYA A., GOSWAMI A. Antifeedant activity and toxicity of leaf extracts from Porteresia coarctata Takeoka and their effects on the physiology of Spodoptera litura (F.). J. Pest Sci. 81, 79, 2008.
  • 32. LIN Y., WAGNER G.J. Surface disposition and stability of pest-interactive, trichome-exuded diterpenes and sucrose esters of tobacco. J. Chem. Ecol. 20, 1907, 1994.
  • 33. LAUE G., PRESTON C.A., BALDWIN I.T. Fast track to the trichome: induction of N-acyl nornicotines precedes nicotine induction in Nicotiana repanda. Planta 210, 510, 2000.
  • 34. HOPKINS R.J., DAM N.M., LOON J.J.A. VAN. Role of glucosinolates in insect-plant relationships and multitrophic interactions. Annu. Rev. Entomol. 54, 57, 2009.
  • 35. SZOŁYGA B., GNIŁKA R., SZCZEPANIK M., SZUMNY A. Chemical composition and insecticidal activity of Tuja occidentalis and Tanacetum vulgare essential oils against larvae of the lesser mealworm, Alphitobius diaperinus. Entomol. Exp. Appl. 151, 1, 2014.
  • 36. LOWE H.J.B. Resistance and susceptibility to colour forms of the aphid Sitobion avenae in spring and winter wheat (Triticum aestivum). Ann. Appl. Biol. 99, 87, 1981.
  • 37. BECK D.L., DUNN G.M., BOWMAN J.S. Biochemical basis of resistance in corn leaf aphid. Crop Sci. 23, 995, 1983.
  • 38. BARENBAUM M.R. Turnabout is fair play: secondary roles for primary compounds. J. Chem. Ecol. 21, 925, 1995.
  • 39. WEI S., SEMEL Y., BRAVDO B.A., CZOSNEK H., SHOSEYOV O. Expression and subcellular compartmentation ofAspergillus niger b-glucosidase in transgenic tobacco result in an increased insecticidal activity on white flies (Be-misia tabaci). Plant Sci. 172, 1175, 2007.
  • 40. WÓJCICKA A. Cereal phenolic compounds as biopesticides of cereal aphids. Pol. J. Environ Stud. 19 (6), 1337, 2010.
  • 41. SIMMONDS M.S.J. Flavonoid-insect interactions: recent advances in our knowledge. Phytochemistry 64, 21, 2003.
  • 42. KHAN M.A.M., ULRICHS CH., MEWIS I. Influecne of water stress on the glucosinolate profile of Brassica oleracea var. italica and the performance of Bravicoryne brassicae and Myzus persicae. Entomol. Exp. Appl. 137, 229, 2010.
  • 43. KHAN M.A.M., ULRICHS CH., MEWIS I. Effect of water stress and aphid herbivory on flavonoids in broccoli (Brassica oleracea var. italica Plenck). J. Appl. Bot. Food Quality, 84, 178, 2011.
  • 44. O'NEILL B.F., ZANGERL A.R., DERMODY O., BILGIN D.D., CASTEEL C.L., ZAVALA J.A., DELUCIA E.H., BARENBAUM M.R. Impact of elevated levels of atmospheric CO2 and herbivory on flavonoids of soybean (Glycine max L.). Chem. Ecol. 36, 35, 2010.
  • 45. SCHMIDT S., ZIETZ M., SCHREINER M., ROHN S., KROH L.W., KRUMBEIN A. Genotypic and climatic influences on the concentration and composition of flavonoids in kale (Brassica oleracea var. sabellica). Food Chem. 119, 1293, 2010.
  • 46. ALONSO C., OSSIPOVA S., OSSIPOV.V. A high concentration of glucogallin the common precursor of hydrolysable tannins, does not deter hrbivores. J. Insect Behav. 15, 649, 2002.
  • 47. HARE J.D. Seasonal variation in the leaf resin components ofMimulus aurantiacus. Biochem Syst. Ecol. 30, 709, 2002.
  • 48. LEISS K.A., MALTESE F., CHOI Y.H, ABDEL-FARID I.B., VERPOORTE R., KLINKHAMER P.G.L. NMR metabolomics of Thrips (Frankliniella occidentalis) resistance in Senecio hybrids. J. Chem. Ecol. 35, 219, 2009.
  • 49. BENNETT R.N., WALLSGROVE R.M. Secondary metabolites in plant defence mechanisms. New Phytologist 127, 617, 1994.
  • 50. ONYILAGHA J.C., LAZORKO J., GRUBER M.Y., SOROKA J.J., ERLANDSON M.A. Effect of flavonoids on feeding preference and development of the crucifer pest Mames-tra configurata Walker. J. Chem. Ecol. 30, 109, 2004.
  • 51. KIRK H., CHOI Y.H., KIM H.K., VERPORTE R., VAN DER MEIJDEN E. Comparing metabolomes: the chemical consequences of hybridization in plants. New Phytol. 167, 613, 2005.
  • 52. WU B., TAKAHASHI T., KASHIWAGI T., TEBAYASHI S.I., KIM C.S. New flavonoid glycosides from the leaves of Solidago altissima. Chem. Pharm. Bull. 55, 815, 2007.
  • 53. LATTANZIO V., ARPAIA S., CARDINALI A., DI VE-NERE D., LINSALATA V. Role of endogenous flavanoids in resistance mechanism of Vigna to aphids. J. Agric. Food Chem. 48, 5316, 2000.
  • 54. LAHTINEN M., KAPARI L., HAUKIOJA E., PIHLAJA K. Effect if increased contact of leaf surface flavonoids on the performance of mountain birch feeding sawflies vary for early and late season species. Chemoecology 16, 159, 2006.
  • 55. VALKAMA E., KORICHEVA J., SALMINĘ J-P., HELANDER M., SALONIEMI I., SAIKKONEN, K.A.N.D., PIHLAJA K. Leaf surface traits: overlooked determinants of birch resistance to herbivores and foliar micro-fungi? Trees 19, 191, 2005.
  • 56. ATEYYAT M., ABU-ROMMAN S., ABU-DARWISH M., GHABEISH I. Impact of flavonoids against woolly apple aphid, Eriosoma lanigerum (Hausmann) and its sole parasitoid, Aphelinus mali (Hald.). J. Agric. Sci. 4 (2), 227, 2012.

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Bibliografia

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