Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-28T04:14:36.490Z Has data issue: false hasContentIssue false
  • English
  • Français

Inheritance of photoperiodic control of larval diapause in the Asian corn borer Ostrinia furnacalis (Guenée)

Published online by Cambridge University Press:  17 March 2015

L. Xiao ,
H.M. He ,
P.S. Zhong ,
S. Fu ,
C. Chen  and
F.S. Xue
L. Xiao
Affiliation:
Institute of Entomology, Jiangxi Agricultural UniversityNanchang 330045, China
H.M. He
Affiliation:
Institute of Entomology, Jiangxi Agricultural UniversityNanchang 330045, China
P.S. Zhong
Affiliation:
Department of life Science, HuiZhou University, HuiZhou 516007, China
S. Fu
Affiliation:
Institute of Entomology, Jiangxi Agricultural UniversityNanchang 330045, China
C. Chen
Affiliation:
Institute of Entomology, Jiangxi Agricultural UniversityNanchang 330045, China
F.S. Xue*
Affiliation:
Institute of Entomology, Jiangxi Agricultural UniversityNanchang 330045, China
*
*Author for correspondence Phone: +867913828081 E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

The Asian corn borer, Ostrinia furnacalis enters diapause as fully grown larvae. Owing to geographical variation in photoperiodic control of diapause, the subtropical strain from Hefei city (HF) enters diapause in response to short daylengths, whereas the tropical strain from Ledong county (LD) exhibits almost no diapause under the same conditions. The two strains were used in crosses to study the inheritance of diapause. The HF strain showed a typical long-day response with a critical daylength of approximately14.97 h at 22 °C, 14.60 h at 25 °C and 13.68 h at 28 °C. The LD strain showed weak photoperiodic responses at 22 and 25 °C; and the F1 progeny also showed a long-day response with significantly shorter critical daylength compared with the HF strain. However, the LD × HF (F × M) crosses had significantly longer critical daylengths than HF × LD crosses, indicating a sexual bias in the inheritance of diapause induction, with the male parent having more influence on the F1 progeny. The critical daylength in a backcross to HF was significantly longer than a backcross to LD. Whether the inheritance of diapause fits an additive hypothesis or not depended on photoperiod, with results from different photoperiods showing additive inheritance or incomplete dominance of either diapause or non-diapause. Unlike diapause induction, the duration of diapause for reciprocal crosses was equally influenced by each parent, suggesting that diapause incidence and maintenance are controlled by separate systems in O. furnacalis.

Keywords

Ostrinia furnacalisdiapauseinheritancephotoperiodic responsepaternal effect
Type
Research Papers
Information
Bulletin of Entomological Research , Volume 105 , Issue 3 , June 2015 , pp. 326 - 334
Check for updates
Copyright
Copyright © Cambridge University Press 2015 

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.)

References

Beck, S.D. (1980) Insect Photoperiodism. 2nd edn. New York, Academic Press.Google Scholar
Chen, C., Xia, Q.W., Chen, Y.S., Xiao, H.J. & Xue, F.S. (2012) Inheritance of photoperiodic control of pupal diapause in the cotton bollworm, Helicoverpa armigera (Hübner). Journal of Insect Physiology 58, 1582–1588.Google Scholar
Chen, C., Xiao, L., He, H.M., Xu, J. & Xue, F.S. (2014) A genetic analysis of diapause in crosses of a southern and a northern strain of the cabbage beetle Colaphellus bowringi (Coleoptera: chrysomelidae). Bulletin of Entomological Research 104, 12–18.Google Scholar
Dai, Z.Y., Qin, Q.L., Yang, Y.Z. & Huang, D.L. (2000) The effects of some factors on the diapause induction of Asian corn borer (Ostrinia furnacalis). Acta Ecologica Sinica 20, 620–623, (in Chinese).Google Scholar
Danilevskii, A.S. (1965) Photoperiodism and Seasonal Development of Insects (English Translation). Edinburgh and London, UK, Oliver and Boyd.Google Scholar
Denlinger, D.L. (1986) Dormancy in tropical insects. Annual Review of Entomology 31, 139–264.Google Scholar
Dolezel, D., Vanecková, H., Sauman, I. & Hodkova, M. (2005) Is period gene causally involved in the photoperiodic regulation of reproductive diapause in the linden bug, Pyrrhocoris apterus? Journal of Insect Physiology 51, 655–659.Google Scholar
Du, Z.W. & Cai, W.Q. (1964) A preliminary report on photoperiodic response of the Asian corn borer, Ostrinia furnacalis (Guenée) in Jiangsu. Acta Entomologica Sinica 13, 129–132, (in Chinese).Google Scholar
Gong, H.F., Chen, P., Wang, R., Lian, M.L., Xia, Z.H. & Yan, Y. (1984) The influence of photoperiod and temperature on the diapause of the Asian corn borer Ostrinia furnacalis (Guenée). Acta Entomologica Sinica 27, 280–286, (in Chinese).Google Scholar
Han, B. & Denlinger, D.L. (2009) Mendelian inheritance of pupal diapause in the flesh fly, Sarcophaga bullata . Journal of Heredity 100, 251–255.Google Scholar
Henrich, V.C. & Denlinger, D.L. (1983) Genetic differences in pupal diapause incidence between two selected strains of the flesh fly. Journal of Heredity 74, 371–374.Google Scholar
Hoy, M.A. (1978) Variability in diapause attributes of insects and mites: some evolutionary and practical implications. pp. 101–126 in Dingle, H. and Hegman, J.P. (Eds) Evolution of Insect Migration and Diapause. New York, Springer-Verlag.Google Scholar
Ikten, C., Skoda, S.R., Hunt, T.E., Molina-Ochoa, J. & Foster, J.E. (2011) Genetic variation and inheritance of diapause induction in two distinct voltine ecotypes of Ostrinia nubilalis (Lepidoptera: Crambidae). Annals of the Entomological Society of America 104, 567–575.CrossRefGoogle Scholar
Kawakami, Y., Numata, H., Ito, K. & Goto, S.G. (2010) Dominant and recessive inheritance patterns of diapause in the two-spotted spider mite Tetranychus urticae . Journal of Heredity 101, 20–25.Google Scholar
Kimura, M.T. (1988) Male mating activity and genetic aspects in imaginal diapause of Drosophila triauraria . Entomologia Experimentalis et Applicata 47, 81–89.Google Scholar
King, A.B.S. (1974) Photoperiodic induction and inheritance of diapause in Pionea forficalis (Lepidoptera: Pyralidae). Entomologia Experimentalis et Applicata 17, 397–409.Google Scholar
Lumme, J., Lakovaara, S., Oikarinen, A. & Lokki, J. (1975) Genetics of the photoperiodic diapause in Drosophila littoralis . Hereditas 79, 143–148.Google Scholar
McWatters, H.G. & Saunders, D.S. (1996) The influence of each parent and geographic origin on larval diapause in the blow fly, Calliphora vicina . Journal of Insect Physiology 42, 721–726.Google Scholar
McWatters, H.G. & Saunders, D.S. (1997) Inheritance of the photoperiodic response controlling larval diapause in the blow fly, Calliphora vicina . Journal of Insect Physiology 43, 709–717.Google Scholar
Nylin, S. (2013) Induction of diapause and seasonal morphs in butterflies and other insects: knowns, unknowns and the challenge of integration. Physiological Entomology 38, 96–104.Google Scholar
Qiao, L., Zheng, J.W., Cheng, W.N. & Li, Y.P. (2008) Impact of 4 different artificial fodders on life span of Asian corn borer, Ostrinia furnacalis (Guenée). Journal of Northwest A&F University 36, 109–112.Google Scholar
Raina, A.K., Bell, R.A. & Klassen, W. (1981) Diapause in the pink bollworm: preliminary genetic analysis. Insect science and its application 1, 231–235.Google Scholar
Robinson, R. (1971) Lepidiptera Genetics. Oxford, UK, Pergamon Press.Google Scholar
Saunders, D.S. (2002) Insect Clocks. Amsterdam, The Netherlands, Elsevier.Google Scholar
Shen, R.W., Xue, F.S. & Zhu, X.F. (1988) Studies on voltinism and the date of diapause incidence in the Asian corn borer, Ostrinia furnacalis (Guenée) in the field. Jiangxi Plant Protection 1, 18–19, (in Chinese).Google Scholar
Showers, W.B. (1981) Geographic variation of the diapause response in the European corn borer. pp. 97–111 in Denno, R.F. and Dingle, H. (Eds) Insect Life History Patterns, Habitat and Geographic Variation. New York, Springer.Google Scholar
Showers, W.B., Keaser, A.J., Witkowski, J.F., Clement, S.L., Chiang, H.C. & Sparks, A.N. (1990) Manipulation of larval diapause of the European corn borer (Lepidoptera: Pyralidae) as a potential mechanism of integrated pest management. Environmental Entomology 19, 1311–1319.Google Scholar
Sims, S.R. (1983) Inheritance of diapause induction and intensity in Papilio zelicaon . Heredity 51, 495–500.Google Scholar
Söderlind, L. & Nylin, S. (2011) Genetics of diapause in the comma butterfly Polygoniac-album . Physiological Entomology 36, 8–13.Google Scholar
Suwa, A. & Gotoh, T. (2006) Geographic variation in diapause induction and mode of diapause inheritance in Tetranychus pueraricola . Journal of Applied Entomology 130, 329–335.Google Scholar
Tauber, M.J., Tauber, C.A. & Masaki, S. (1986) Seasonal Adaptations of Insects. USA, Oxford University Press.Google Scholar
Xia, Q.W., Chen, C., Tu, X.Y., Yang, H.Z. & Xue, F.S. (2012) Inheritance of photoperiodic induction of larval diapause in the Asian corn borer Ostrinia furnacalis . Physiological Entomology 37, 185–191.Google Scholar
Zhou, D.R. & He, K.L. (1995) Asian Corn Borer and its Integrated Management. Beijing, Golden Shield Press.Google Scholar