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The Physio-chemical Variation of the Host Plants and Feed Preference of the Ussur Brown Katydid, Paratlanticus ussuriensis (Orthoptera: Tettigoniidae)

갈색여치(Paratlanticus ussuriensis) 기주식물의 이화학적 특성변화와 먹이선호 구명

  • Kim, Myung-Hyun (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Bang, Hea-Son (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Jung, Myung-Pyo (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Na, Young-Eun (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Han, Min-Su (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Kang, Kee-Kyung (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA) ;
  • Lee, Deog-Bae (Agro-Ecosystem, Environmental Ecology Division, National Academy of Agricultural Science, RDA)
  • 김명현 (국립농업과학원 기후변화생태과) ;
  • 방혜선 (국립농업과학원 기후변화생태과) ;
  • 정명표 (국립농업과학원 기후변화생태과) ;
  • 나영은 (국립농업과학원 기후변화생태과) ;
  • 한민수 (국립농업과학원 기후변화생태과) ;
  • 강기경 (국립농업과학원 기후변화생태과) ;
  • 이덕배 (국립농업과학원 기후변화생태과)
  • Published : 2009.12.30

Abstract

In 2006 and 2007, there was a big outbreak of the Ussur Brown Katydid, Paratlanticus ussurriensis in the central part of Korea attacking some orchard trees. Until 2000, the katydid had not been regarded as an agricultural pest because they were distributed widely in Korea with low population density and their habitats were confined mainly to hillsides of forested areas. The fact that katydid attacked orchard trees with a higher population density seemed to be related to a change in feeding environment. And the shift of their habitats from oak woodlands to commercial orchards was thought to be related to the nutritional contents of their feed. In an attempt to understand these relationships, we conducted an ecological study of the affected areas. When the katydids changed their habitats in early May of 2008 and 2009, they shifted their host plants from oak trees to peach trees. The habitat shift was closely related to the nitrogen (N) content of the host plant leaves. When katydid moved to the hillside adjacent to orchard farm, N content of oak tree leaves decreased dramatically from 5.3% to 2.2%. At that time N content of peach tree leaves were higher than the 2.2% of oak leaves, showing 3.5~5.0%. This range of N content of peach tree leaves has been consistent until late June. And feed preference analysis carried out in the laboratory showed that katydid prefered peach tree leaves to peach fruit to oak tree leaves.

Keywords

References

  1. Ahn, K. S., Yang, J. O., Noh, D. J., Yoon, C. and Kim, G. H. (2007) Susceptibility of ussur brown katydid, Paratlanticus ussuriensis (Orthoptera: Tettigoniidae) to commercially registered insecticides, Kor. J. Pestic. Sci. 11, 194-200
  2. Bang, H. S., Na, Y. E., Han, M. S., Kim, M. H., Roh, K. A. and Lee, J. T. (2008) Ovipositional characteristics of the ussur brown katydid, Paratalanticus ussuriensis (Orthoptera: Tettigoniidae), Kor. J. Environ. Agr. 27, 274-278 https://doi.org/10.5338/KJEA.2008.27.3.274
  3. Noh, D. J., Yang, J. O., Moon, S. R., Yoon, C., Kang, S. H., Ahn, K. S. and Kim, G. H. (2008) Attractants and trap development for ussur brown katydid, Paratlanticus ussuriensis (Orthoptera: Tettigoniidae), Kor. J. Pestic. Sci. 12, 256-261
  4. Uvarov, B. P. (1926) Some Orthoptera from the Russian Far East, Ann. Mag. Natl. Hist. 17, 273-291
  5. Kim, T. W. (2001) Taxonomy of Korean Tettigonioidae (Orthoptera: Ensifera). Thesis for the degree of master in the department of biology graduate school, Sungshin Women's University. Korean. p. 59-6
  6. Bang, H. S., Kim, M. H., Jung, M. P., Han, M. S., Na, Y. E., Kang, K. K., Lee, D. B. and Lee, K. Y. (2009) Effects of chilling and overwintering temperature conditions on the termination of egg diapause of the ussur brown katydid Paratlanticus ussuriensis, Kor. J. Appl. Entomol. 48, 221-227 https://doi.org/10.5656/KSAE.2009.48.2.221
  7. Hewitt, G. B. (1977) Hatching and development of rangeland grasshoppers in relation to forage growth, temperature, and precipitation, Environ. Entomol. 8, 24-29.
  8. Anderson, N. L. (1961) Seasonal losses in rangeland vegetation due to grasshoppers, J. Econ. Entomol. 54, 369-378 https://doi.org/10.1093/jee/54.2.369
  9. Anderson, N. L. (1964) Some relationships between grasshoppers and vegetation, Ann. Entomol. Soc. Am. 57, 736-742 https://doi.org/10.1093/aesa/57.6.736
  10. Na, Y. E., Bang, H. S., Kim, M. H., Oh, Y. J., Han, M. S., Kim, M. K., Roh, K. A., Lee, J. T. and Choi, D. R. (2007) The characteristic on egg-laying and vegetation grazing of Paratlanticus ussuriensis, Korean J. Environ. Agr. 26, 364 366 https://doi.org/10.5338/KJEA.2007.26.4.364
  11. Kim, J. W. (1992) Vegetation of Northeast Asia: On the syntaxonomy and syngeography of the oak and beech forests. Ph. D. Dissertation of the University of Vienna. p. 314
  12. Kim, J. W. (1990) Syntaxonomic scheme for the deciduous oak forests in South Korea, Abstr. Bot. 14, 51-81
  13. Bernays, E. A. (1982) The insect on the plant- a closer look. In: Visser J. H., Minks A. K. (eds) Proceedings 5th international symposium on insect-plant relationships. Pudoc, Wageningen, p. 3-17
  14. Ohmart, C. P., Stewart, L. G. and Thomas, J. R. (1985) Effects of food quality, particularly nitrogen concentrations, of Eucalyptus blakelyi foliage on the growth of Paropsis atomaria larvae (Coleoptera: Chrysomelidae), Oecologia. 65, 543-549 https://doi.org/10.1007/BF00379670
  15. Dadd, R. H. (1985) Nutrition: organisms. In: Kerkut G.A., Gilbert L.I.(eds) Comparative insect phusiology, biochemistry and pharmacology, vol 4. Pergammon, Oxford, p. 177-217
  16. Hinks, C. F., Hupka, D. and Olfert, O. (1993) Nutrition and the protein economy in grasshoppers and locusts, Comp. Physiol. 104A, 133-142
  17. Slansky, F. (1982) Insect nutrition: an adaptationist's perspective, Florida Entomol. 65, 45-71 https://doi.org/10.2307/3494145
  18. White T. C. R. (1984) The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants, Oecologia. 63, 90-105 https://doi.org/10.1007/BF00379790
  19. Mattson, W. J. and Haack. R. A. (1987) The role of drought in outbreaks of plant-eating insects, Bioscience. 37, 110-118 https://doi.org/10.2307/1310365
  20. Joern, A. and Gaines, S. B. (1990) Population dynamics and regulation in grasshoppers. In: Chapman, R. F., Joern, A. (eds) Biology of grasshoppers. Wiley, New York, p. 415-482
  21. Brunt, C., Read, J. and Sanson, G. D. (2006) Changes in resource concentration and defence during leaf development in a tough-leaved (Nothofagus moorei) and soft-leaved (Toona ciliata) species, Oecologia. 148, 583-592 https://doi.org/10.1007/s00442-006-0369-4
  22. Schroeder, L. A. (1986) Changes in tree leaf quality and growth performance of Lepidopteran larvae, Ecology. 67, 1628-1636 https://doi.org/10.2307/1939094
  23. Feeny, P. (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars, Ecology. 51, 565-581 https://doi.org/10.2307/1934037
  24. Pais, M. P. and Varanda, E. M. (2003) Variation in plant defenses of Didymopanax vinosum (Cham. & Schltdl.) Seem. (Apiaceae) across a vegetation gradient in a Brazilian cerrado. Acta bot. bras. 17, 395-403
  25. Kim, C. W. (1984) A study on the distributions of butterflies and of their feeding plants in Korea, Ent. Res. Bull. 10, 35-124
  26. Evans, A. R. and Sanson, G. D. (2005) Biomechanical properties of insects in relation to insectivory: cuticle thickness as an indicator of insect 'hardness' and 'intractability', Aus. J. Zool. 53, 9-19 https://doi.org/10.1071/ZO04018
  27. White, T. C. R. (1976) Weather, food and plagues of locusts, Oecologia. 22, 119 134 https://doi.org/10.1007/BF00344712
  28. Jones, C. G. and Coleman, J. S. (1992) Plant stress and insect herbivory: toward an integrated perspective. In: Mooney H. A., Winner W. E., Pell, E. J. (eds). Response of plants to multiple stresses. Academic Press, San Diego, p. 249-280
  29. Anthony, J. and Spencer, T. B. (1997) Importance of dietary nitrogen and carbohydrates to survival, growth, and reproduction in adults of the grasshopper Ageneotettix deorum (Orthoptera: Acrididae), Oecologia. 112, 201-208 https://doi.org/10.1007/s004420050301
  30. Abisgold, J. D. and Simpson, S. J. (1987) The physiology of compensation by locusts for changes in dietary protein, J. Exp. Biol. 129, 329-346
  31. Van Heusdon, M. C., Van der Horst, D. J., Voshol, J. and Beenakkers, A. M. (1987) The recycling of protein components of the flight-specific lipophorin in Locusta migratoria, Insect Biochem. 17, 771-776 https://doi.org/10.1016/0020-1790(87)90048-5
  32. Lewis, A. C. (1984). Plant quality and grasshopper feeding: effects of sunflower condition on preference and performance in Melanoplus differentialis, Ecology. 65, 836-843 https://doi.org/10.2307/1938057
  33. David C. L. and Whitford, W. G. (1987) Variation in insect densities on desert creosotebush: Is nitrogen a factor?, Ecology. 68, 547-557 https://doi.org/10.2307/1938460
  34. Rausher M. D. (1981) Host plant selection by Battus philenor Butterflies: The roles of predation, nutrition, and plant chemistry, Ecol. Monogr. 51, 2-20

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