Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-23T11:37:19.463Z Has data issue: false hasContentIssue false
  • English
  • Français

Effects of temperature on instar number and larval development in the endangered longhorn beetle Callipogon relictus (Coleoptera: Cerambycidae) raised on an artificial diet

Published online by Cambridge University Press:  21 June 2019

Dae-Am Yi ,
Alexander V. Kuprin  and
Yeon Jae Bae
Dae-Am Yi
Affiliation:
Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea
Alexander V. Kuprin
Affiliation:
Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok-22, 690022, Russia
Yeon Jae Bae*
Affiliation:
Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea Laboratory of Biodiversity and Ecology, Division of Environmental Science and Ecological Engineering, College of Life Sciences and Biotechnology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea
*
1Corresponding author (e-mail: yjbae@korea.ac.kr)
Get access Rights & Permissions [Opens in a new window]

Abstract

Callipogon relictus Semenov (Coleoptera: Cerambycidae) is currently listed in the Red Data Books (Category I) of Russia and South Korea and, in 2006, was designated by the South Korean government as the first invertebrate priority target species in a restoration project. However, the species is also classified as an invasive quarantine pest by the Canadian Food Inspection Agency. Due to the five-year to seven-year life cycle of the species, experimental information about instar numbers has been poorly documented. Therefore, the goal of the present study was to document the instar numbers of non-diapause Callipogon relictus larvae reared on an artificial diet. Under conditions of 30 °C, 60% relative humidity, and constant dark (0:24 hour light-dark photoperiod), developmental pathways of 8, 10, and 12 instars were observed. The effect of temperature (20, 25, and 30 °C) on the duration of larval development was also examined to identify the optimum temperature for producing Callipogon relictus for conservational purposes. Larvae reared at 30 °C and 60% relative humidity, without a chill period, developed in seven to eight months, which is about one-tenth the duration of C. relictus development under natural conditions and the most rapid development of C. relictus observed to date.

Type
Techniques
Information
The Canadian Entomologist , Volume 151 , Issue 4 , August 2019 , pp. 537 - 544
Copyright
© Entomological Society of Canada 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Subject editor: David Siaussat

References

Angilletta, M.J. and Dunham, A.E. 2003. The temperature-size rule in ectotherms: simple evolutionary explanations may not be general. The American Naturalist, 162: 332–342.CrossRefGoogle Scholar
Beer, F.M. 1949. The rearing of Buprestidae and delayed emergence of their larvae. The Coleopterists Bulletin, 3: 81–84.Google Scholar
Canadian Food Inspection Agency. 2010. Phytosanitary requirements for the importation and domestic movement of firewood. D-01-12 (second revision). Canadian Food Inspection Agency, Ottawa, Ontario, Canada.Google Scholar
Choudhuri, D.K. 1963. Temperature and its effects on three species of genus Onychiurus . Proceedings of the Zoological Society, 13: 123–128.Google Scholar
Danks, H.V. 2000. Measuring and reporting life-cycle duration in insects and arachnids. European Journal of Entomology, 97: 285–303.CrossRefGoogle Scholar
Drummond, F.A., James, R.L., Casagrande, R.A., and Faubert, H. 1984. Development and survival of Podisus maculiventris (Say) (Hemiptera: Pentatomidae), a predator of the Colorado potato beetle (Coleoptera: Chrysomelidae). Environmental Entomology, 13: 1283–1286.CrossRefGoogle Scholar
Flaherty, L., Régnière, J., and Sweeney, J. 2012. Number of instars and sexual dimorphism of Tetropium fuscum (Coleoptera: Cerambycidae) larvae determined by maximum likelihood. The Canadian Entomologist, 144: 720–726.CrossRefGoogle Scholar
Greene, E. 1988. A diet-induced developmental polymorphism in a caterpillar. Science, 243: 643–646.CrossRefGoogle Scholar
Howe, R.W. 1967. Temperature effects on embryonic development in insects. Annual Review of Entomology, 12: 15–42.CrossRefGoogle ScholarPubMed
Hunt, G. and Chapman, R.E. 2001. Evaluating hypotheses of instar-grouping in arthropods: a maximum likelihood approach. Paleobiology, 27: 466–484.2.0.CO;2>CrossRefGoogle Scholar
Iba, M. 1988. Rearing of the yellow spotted longicorn beetle, Psacothea hilaris with an artificial diet. The Nature and Insect, 23: 7–12. [In Japanese].Google Scholar
Klingenberg, C.P. and Zimmermann, M. 1992. Dyar’s rule and multivariate allometric growth in nine species of waterstriders (Heteroptera: Gerridae). Journal of Zoological Society of London, 227: 453–464.CrossRefGoogle Scholar
Kuprin, A.V. and Bezborodov, V.G. 2012. Areal of Callipogon relictus Semenov, 1899 (Coleoptera, Cerambycidae) in the Russian Far East. Biology Bulletin, 39: 387–391.CrossRefGoogle Scholar
Kuprin, A.V., Bezborodov, V.G., Yi, D.A., and Kotlyar, A.K. 2014. Developmental biology and ecological peculiarities of the relic longhorn beetle Callipogon relictus Semenov, 1899 (Coleoptera, Cerambycidae). Entomological Review, 94: 1251–1256.CrossRefGoogle Scholar
Lamb, R.J., MacKay, P.A., and Gerber, G.H. 1987. Are development and growth of pea aphids, Acyrthosiphon pisum, in North America adapted to local temperatures? Oecologia, 72: 170–177.CrossRefGoogle ScholarPubMed
Li, J., Drumont, A., Zhang, X., Gao, M., and Zhou, W. 2012. The checklist of Northeast China’s subfamily Prioninae and biological observations of Callipogon relictus Semenov-Tian-Shanskij, 1899 (Coleoptera, Cerambycidae, Prioninae). Les Cahiers Magellanes, 9: 50–56.Google Scholar
Li, J., Drumont, A., Zhang, X., and Lin, L. 2013. Note on the egg productivity of females of Callipogon (Eoxenus) relictus, Semenov-Tian-Shanskij, 1899, and first record for Inner Mongolia Autonomous Region in China (Coleoptera, Cerambycidae, Prioninae). Les Cahiers Magellanes, 12: 52–56.Google Scholar
Loerch, C.R. and Cameron, E.A. 1983. Determination of larval instars of the bronze birch borer, Agrilus anxius (Coleoptera: Buprestidae). Annals of the Entomological Society of America, 76: 948–952.CrossRefGoogle Scholar
Lupi, D., Jucker, C., Rocco, A., Cappellozza, S., and Colombo, M. 2015. Diet effect on Psacothea hilaris hilaris (Coleoptera: Cerambycidae) performance under laboratory conditions. International Journal of Agriculture Innovations and Research, 4: 97–104.Google Scholar
Munyiri, F.N., Shintani, Y., and Ishikawa, Y. 2004. Evidence for the presence of a threshold weight for entering diapause in the yellow-spotted longicorn beetle, Psacothea hilaris . Journal of Insect Physiology, 50: 295–301.CrossRefGoogle ScholarPubMed
National Institute of Biological Resources. 2013. Red data book of endangered insects in Korea (II). National Institute of Biological Resources, Incheon, South Korea. [In Korean].Google Scholar
Naves, P.M., Sousa, E., and Rodrigues, J.M. 2008. Biology of Monochamus galloprovincialis (Coleoptera, Cerambycidae) in the pine wilt disease affected zone, southern Portugal. Silva Lusitana, 16: 133–148.Google Scholar
Panzavolta, T. 2007. Instar determination for Pissodes castaneus (Coleoptera: Curculionidae) using head capsule widths and lengths. Environmental Entomology, 36: 1054–1058.CrossRefGoogle ScholarPubMed
Pershing, J.C. and Linit, M.J. 1988. Variation in number of instars of Monochamus carolinensis (Coleoptera: Cerambycidae). Journal of the Kansas Entomological Society, 61: 370–378.Google Scholar
Rasmussen, S. 1967. Growth of larvae of the house longhorn beetle (Hylotrupes bajulus L.) in constant conditions. Oikos, 18: 155–177.CrossRefGoogle Scholar
Red Book of Amur Province. 2009. An official list of rare and endangered species of animals, plants, and fungi. Blagoveshchensk State Pedagogical University, Blagoveshchensk, Russia. [In Russian].Google Scholar
Ruberson, J.R., Tauber, M.J., and Tauber, C.A. 1986. Plant feeding by Podisus maculiventris (Heteroptera: Pentatomidae): effect on survival, development, and preoviposition period. Environmental Entomology, 15: 894–897.CrossRefGoogle Scholar
Semenov, A.P. 1899. Callipogon (Eoxenus) relictus, sp. n., a representative of the Neotropical genus of Cerambycidae in the Russian fauna. Trudy Russkago Entomologicheskago Obshchestva, 32: 562–580. [In Russian].Google Scholar
Smith, D.N. 1962. Prolonged larval development in Buprestis aurulenta L. (Coleoptera: Buprestidae), a review with new cases. The Canadian Entomologist, 94: 586–593.CrossRefGoogle Scholar
Štefková, K., Okrouhlik, J., and Dolezal, P. 2017. Development and survival of the spruce bark beetle, Ips typographus (Coleoptera: Curculionidae: Scolytinae) at low temperatures in the laboratory and the field. European Journal of Entomology, 114: 1–6.Google Scholar
Trotter, R.T. and Keena, M.A. 2016. A variable-instar climate-driven individual beetle-based phenology model for the invasive Asian longhorned beetle (Coleoptera: Cerambycidae). Environmental Entomology, 45: 1360–1370.CrossRefGoogle Scholar
Yi, D.A. 2014. Breeding & restoration of Korean relic long-horned beetle: Callipogon relictus, National Institute of Biological Resources, Inchon, South Korea.Google Scholar
Yi, D.A., Kuprin, A.V., and Bae, Y.J. 2018. Distribution of the longhorned beetle Callipogon relictus (Coleoptera: Cerambycidae) in northeast Asia. Zootaxa, 4369: 101–108.CrossRefGoogle Scholar
Yi, D.A., Kuprin, A.V., Lee, Y.H., and Bae, Y.J. 2017. Newly developed fungal diet for artificial rearing of the endangered long-horned beetle Callipogon relictus (Coleoptera: Cerambycidae). Entomological Research, 47: 373–379.CrossRefGoogle Scholar
Supplementary material: PDF

Yi et al. supplementary material

Yi et al. supplementary material 1

Download Yi et al. supplementary material(PDF)
PDF 103.5 KB