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Thursday, 17 November 2016

Horizontal niche differentiation of ambrosia beetles (Coleoptera: Scolytidae and Platypodidae) within the standing trunk of Quercus serrata

Published Date
Volume 21, Issue 6pp 319–323

Short Communication
DOI: 10.1007/s10310-016-0546-1

Cite this article as: 
Iidzuka, H. & Osawa, N. J For Res (2016) 21: 319. doi:10.1007/s10310-016-0546-1

Author
Abstract

Niche differentiation, in terms of time and space, has been reported within a community of ambrosia beetles (Coleoptera: Scolytidae and Platypodidae) in a tree trunk. Two platypodid ambrosia beetles, Platypus quercivorus (Murray) and Platypus calamus Blandford, utilize a similar height range with respect to the Quercus serrata Murray (Fagaceae) trunk. The sapwood and heartwood (i.e., wood types) are known to differ in their physical and chemical characteristics. The objective of this study was to determine the differences among ambrosia beetles, in terms of wood type preferences, in a Qserrata tree trunk. We analyzed the horizontal distribution patterns of ambrosia beetles within two mature Qserrata tree trunks. Platypus calamus and the other ambrosia beetles [PquercivorusAmbrosiodmus lewisi (Blandford), Ambrosiophilus atratus Eichhoff, and Xyleborus sp.] showed different horizontal distribution patterns within the wood. The former tended to utilize the heartwood, whereas the latter utilized the sapwood. These results suggest that the wood type can be regarded as one of the niche dimensions of ambrosia beetles in a Qserrata trunk.

References

  1. Beaver RA (1989) Insect–fungus relationships in the bark and ambrosia beetles. In: Wilding N, Collins NM, Hammond PM, Webber JF (eds) Insect–fungus interactions. 14th Symposium of the Royal Entomological Society of London in collaboration with the British Mycological Society. Academic, London, pp 121–143Google Scholar
  2. Begon M, Harper JL, Townsend CR (1986) The influence of competition on community structure. In: Begon M, Harper JL, Townsend CR (eds) Ecology: individuals, populations and communities. Blackwell, Oxford, pp 670–699Google Scholar
  3. Dyer EDA, Chapman JA (1965) Flight and attack of the ambrosia beetle, Trypodendron lineatum (Oliv.) in relation to felling date of logs. Can Entomol 97:42–57CrossRefGoogle Scholar
  4. Hijii N, Kajimura H, Urano T, Kinuura H, Itami H (1991) The mass mortality of oak trees induced by Platypus quercivorus (Murayama) and Platypus calamus Blandford (Coleoptera: Platypodidae). The density and spatial distribution of attack by the beetles. J Jpn For Soc 73:471–476Google Scholar
  5. Horikawa Y (1972) Atlas of the Japanese Flora. Gakken, TokyoGoogle Scholar
  6. Hulcr J, Mogia M, Isua B, Novotny V (2007) Host specificity of ambrosia and bark beetles (Col., Curculionidae: Scolytinae and Platypodinae) in a New Guinea rainforest. Ecol Entomol 32:762–772CrossRefGoogle Scholar
  7. Iidzuka H, Goto H, Yamasaki M, Osawa N (2014) Ambrosia beetles (Curculionidae: Scolytinae and Platypodinae) on Fagus crenata Blume: community structure, seasonal population trends, and resource utilization patterns. Entomol Sci 17:167–180CrossRefGoogle Scholar
  8. Iidzuka H, Goto H, Osawa N (2016) Gallery diameter of ambrosia beetles (Coleoptera: Scolytidae, Platypodidae) and insect fauna in Quercus serrata suffering from Japanese oak wilt. Appl Entomol Zool 51:421–427CrossRefGoogle Scholar
  9. Institute SAS (2013) JMP statistical discovery software, version 11.2.1. SAS Institute, CaryGoogle Scholar
  10. Kabe M (1960) Catalogue of scolytid and platypodid-beetles classified by host tree species. In: On the hosts and habitats of the Scolytid and Platypodid-beetles in Japan. Maebashi Regional Forest Office, Maebashi pp 94–160 (in Japanese)
  11. Kinuura H (2002) Relative dominance of the mold fungus, Raffaelea sp., in the mycangium and proventriculus in relation to adult stages of the oak platypodid beetle, Platypus quercivorus (Coleoptera; Platypodidae). J For Res 7:7–12CrossRefGoogle Scholar
  12. Kinuura H, Kobayashi M (2006) Death of Quercus crispula by inoculation with adult Platypus quercivorus (Coleoptera: Platypodidae). Appl Entomol Zool 41:123–128CrossRefGoogle Scholar
  13. Kubono T, Ito S (2002) Raffaelea quercivora sp. nov. associated with mass mortality of Japanese oak, and the ambrosia beetle (Platypus quercivorus). Mycoscience 43:255–260CrossRefGoogle Scholar
  14. Kühnholz S, Borden JH, Uzunovic A (2001) Secondary ambrosia beetles in apparently healthy trees: adaptations, potential causes and suggested research. Integr Pest Manag Rev 6:209–219CrossRefGoogle Scholar
  15. Kuroda K (2013) Discoloration of sapwood occurring in the forests. Wood Prot 39:2–6 (in Japanese)CrossRefGoogle Scholar
  16. Meerts P (2002) Mineral nutrient concentrations in sapwood and heartwood: a literature review. Ann For Sci 59:713–722CrossRefGoogle Scholar
  17. Nobuchi A (1973) The Platypodidae of Japan (Coleoptera). Bull Gov For Exp Sta 256:1–22Google Scholar
  18. Okada N, Katayama Y, Nobuchi T, Ishimaru Y, Aoki A (1993) Trace elements in the stems of trees, 6: Comparisons of radial distributions among hardwood stems. Mokuzai Gakkaishi 39:1119–1127Google Scholar
  19. Oliver JB, Mannion CM (2001) Ambrosia beetle (Coleoptera: Scolytidae) species attacking chestnut and captured in ethanol-baited traps in middle Tennessee. Environ Entomol 30:909–918CrossRefGoogle Scholar
  20. Roberts H (1977) The Platypodidae (Coleoptera) of Fiji (with descriptions of two new species). J Nat Hist 11:555–578CrossRefGoogle Scholar
  21. Saito S, Nakamura H, Miura N, Onose K (1999) Pesticide treatment on the oak dieback in Japan. For Pest 48:84–94 (in Japanese)Google Scholar
  22. Saito S, Nakamura H, Okada M, Honma K (2014) Preventive effect of trunk injection of benomyl wettable powder on mass mortality of oak trees. Jpn J Pest Sci 39:10–17 (in Japanese with English abstract)CrossRefGoogle Scholar
  23. Sanguansub A, Goto H, Kamata N (2012) Guild structure of ambrosia beetles attacking a deciduous oak tree Quercus serrata in relation to wood oldness and seasonality in three locations in the Central Japan. Entomol Sci 15:42–55CrossRefGoogle Scholar
  24. Schoener TW (1974) Resource partitioning in ecological communities. Science 185:27–39CrossRefPubMedGoogle Scholar
  25. Schroeder LM (1992) Olfactory recognition of nonhosts aspen and birch by conifer bark beetles Tomicus piniperda and Hylurgops palliatus. J Chem Ecol 18:1583–1593CrossRefPubMedGoogle Scholar
  26. Siitonen J (2012) Microhabitats. In: Stackland JN, Siitonen J, Jonsson BG (eds) Biodiversity in dead wood. Cambridge University Press, New York, pp 150–182CrossRefGoogle Scholar
  27. Soné K, Mori T, Ide M (1998) Spatial distribution pattern of attack of the oak borer, Platypus quercivorus (Murayama) (Coleoptera: Platypodidae), and Scolytid ambrosia beetles (Coleoptera: Scolytidae). J For Res 3:225–229CrossRefGoogle Scholar
  28. Takizawa H, Hayami K, Kubota J, Tsukamoto Y (1996) Variations of volume water content and water potential in tree stems because of transpiration. J Jpn For Soc 78:225–230 (in Japanese with English abstract)Google Scholar
  29. Utsumi Y (2013) Analytical methods for water distribution and water movement in secondary xylem of trees. J Jpn Wood Res Soc 59:1–12 (in Japanese with English abstract)CrossRefGoogle Scholar
  30. Yamasaki M, Sakimoto M (2009) Predicting oak tree mortality caused by the ambrosia beetle Platypus quercivorus in a cool-temperate forest. J Appl Entomol 133:673–681CrossRefGoogle Scholar
  31. Yazawa K (1960) The seasonal water content of sapwood and heartwood or broad-leaved trees, especially of beech (Fagus crenata Blume). Mokuzai Gakkaishi 6:170–175 (in Japanese with English abstract)Google Scholar

For further details log on website :
http://link.springer.com/article/10.1007/s10310-016-0545-2

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