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Inherited sterility in different strains of Ephestia cautella (Lepidoptera: Pyralidae)

Published online by Cambridge University Press:  19 September 2011

Ayad A. Al-Taweel ,
Mohammed S.H. Ahmed ,
Sarab S. Kadhum ,
Asaad A. Hameed  and
Majdolin J. Nasser
Ayad A. Al-Taweel
Affiliation:
Agriculture and Biology Faculty, P. O. Box 765, Baghdad, Iraq
Mohammed S.H. Ahmed
Affiliation:
Agriculture and Biology Faculty, P. O. Box 765, Baghdad, Iraq
Sarab S. Kadhum
Affiliation:
Agriculture and Biology Faculty, P. O. Box 765, Baghdad, Iraq
Asaad A. Hameed
Affiliation:
Agriculture and Biology Faculty, P. O. Box 765, Baghdad, Iraq
Majdolin J. Nasser
Affiliation:
Agriculture and Biology Faculty, P. O. Box 765, Baghdad, Iraq
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Abstract

Partial sterility induced by gamma irradiation of Ephestia cautella adult males was studied in five laboratory strains (A,B,C,D and E) which exhibit conspicuous genetic variation in the adult forewing pigmentation. Four of these strains had been reared in the laboratory for more than 80 generations, while the fifth strain has been reared for only 10 generations. When males irradiated with 0.2 kGy were crossed with untreated females, the per cent egg hatch was reduced significantly as compared to the unirradiated control crosses. Strain C showed the highest reduction in the per cent egg hatch followed by a gradual decrease in radiation sensitivity in strains A,E,D and B, respectively. Fecundity and mating frequency appeared not to be affected but the sex ratios were clearly distorted (about two males to one female) in all strains. F1 progeny of all strains were either sterile when mated together (per cent egg hatch = 0.0%), but semi sterile when F1 males were mated to normal females (per cent egg hatch = 0.03–3.95 %). Low fertility was observed when F1 females were mated with normal males (per cent egg hatch = 1.30–15.04%). The cytogenetical investigations showed spermatogenesis to proceed normally in the F1 males, whose fathers had been irradiated (0.2 kGy). However, the primary spermatocyte cells carried multiple chromosomal translocations which were the main cause of the sterility in the F1 males.

Résumé

La stérilité partielle a été provoqueé par l'irradiation de gamma chez les cing mâles adultes de Ephestia cautella souches de laboratoire (nommées A,B,C,D, et E). Les adults deces souches exposent une visible pigmentation sur l'aile antérieure commeune variation génétique. Les quatre premeiére souches ont été élevees dans le laboratoire plusque 80 génération, tandisque la cinquieme jusquá 10 génération. Léclosion des aeufs ont été diminuees significativement qundune femelle normal croisée avec un mâle irradié de 0.2 kGy de rayons gamma en comporaison avec celles non-irradiee. On a constaté que l'effet d'irradiation sur léclosion des oeufs de souche C soit plusque lesautres, mals l'effet a diminue progressivement sur les A, E, D, et B, la proportion de sex ontété dénaturee (2 mâle: 1 femelle) chertoutes les souches apres lirradiation, mais la frequence deléclosion et l'union restaient presque normal. D'autre côté la stérilité était total chez les F1 de toutes souches quand on se croisé entre aux, et entre 0.0–3.95% quand une femelle normal croisee avec une F1 male irradié. On observé ainssi, une faiblé fertilité quand les deux F1 normal sáccoupler (eclosion de 1.3 á 15.04%).

Finalement, notre etudent cytogénétiques ont montrees quele déroulement dela spermatogenésé etait normal chez les mâles des F1 provenant de souches irradiees, male leur cellule spermatocyte apportent une translocation multiple celle aberration chromosomique aète trés prolalement la cause principle dela stérilité chez les males eu F1.

Keywords

Inherited sterilityF1-sterilityEphestia cautellastored product pestgamma radiation
Type
Research Articles
Information
International Journal of Tropical Insect Science , Volume 10 , Issue 4 , August 1989 , pp. 463 - 469
Copyright
Copyright © ICIPE 1989

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References

REFERENCES

Ahmed, M.S.H., Al-Hakkak, Z.S., and Al-Saqur, A.M. (1971) Exploratory studies on the possibility of integrated control of the fig moth, Ephestia cautella (Walk.). Application of Induced Sterility for Control of Lepidoptera Populations (Proc. Panel, Vienna, 1970) IAEA pp. 1–6.Google Scholar
Ahmed, M.S.H., Al-Hakkak, Z.S. and Al-Saqur, A. M. (1972) Inherited sterility in the fig moth Cadra (Ephestia) cautella (Walk.). Int. Conf. Peaceful Uses Atom. Energy (Proc. Conf. Geneva, 1971) UN, Vienna 12. pp. 383–389.Google Scholar
Ahmed, M.S.H., Lamooza, S.B., Ouda, N.A. and Al-Hassany, I.A. (1975) Preliminary report on mating studies of three varieties of Cadra (Ephestia) cautella (Walk.). Sterility Principle for Insect Control, (Proc. Symp. Innsbruck, 1974). IAEA, Vienna. pp. 413–421.Google Scholar
Ahmed, M.S.H., Al-Taweel, A.A., Ouda, N.A., Lamooza, S.B. and Al-Hassany, I.A. (1975a) Colour inheritance in the forewings of Ephestia cautella. 1st. Congr. Iraq Atom. Energy Comm. (Proc. Congr. Baghdad, 1975) Baghdad, pp. 89–95.Google Scholar
Ahmed, M.S.H. (1976) General information regarding the status of dry dates disinfestation in Iraq. A report submitted to the joint FAO/IAEA Research Coordination Meeting on Technological and Economical Feasibility of Food Irradiation, Wageningen, The Netherlands.Google Scholar
Ahmed, M. S. H, Kadhum, A. A., Hameed, A. A., Ali, S. R. and Al-Hakkak, Z. S. (1984) Cytoplasmic analysis of Ephestia cautella adult females collected in different regions of Iraq. J. stored. Prod. Res. 20, 151–152.CrossRefGoogle Scholar
Ahmed, M.S.H. (1988) Cytoplasmic incompatibility for suppression of Ephestia cautella infestation rate in simulated date stores. Modern Insect Control: Nuclear Techniques and Biotechnology (Proc. Symp. Vienna, 1987). IAEA, Vienna, pp. 102–103.Google Scholar
Amoako-Atta, B. and Partida, G. J. (1976) Sensitivity of almond moth pupae to gamma radiation (Lepidoptera: Pyralidae). J. Kans. entomol. Soc. 49, 133–140.Google Scholar
Amoako-Atta, B., Denell, R.E. and Mills, R.B. (1978) Radiation-induced sterility in Ephestia cautella (Walker) (Lepidoptera: Pyralidae): Recovery of fertility during five generations after gamma irradiation. J. stored Prod. Res. 14, 181–188.CrossRefGoogle Scholar
Al-Hakkak, Z.S., Ali, S. R. and Ahmed, M.S.H. (1982) Differential sterility induced by gamma radiation in the adult males of six strains of Ephestia cautella. Sterile Insect Technique and Radiation in Insect Control IAEA, Vienna, pp. 434–436.Google Scholar
Al-Taweel, A.A. and Fox, D.P. (1983) Germ cell differentiation and kinetics in the testes of Dermestes (Coleoptera). Cytologia 48, 605–620.CrossRefGoogle Scholar
Brower, J.H. (1979) Radiosensitivity of adults of the almond moth. J. econ. entomol. 72, 43–47.CrossRefGoogle Scholar
Brower, J. H. (1980) Inheritance of partial sterility in progeny of irradiated males Ephestia cautella (Lepidoptera: Pyralidae) and its effect on theoretical population suppression. Can. Entomol. 112, 131–140.CrossRefGoogle Scholar
Carpenter, J.E., Young, J. R., Sparks, A. N., Cromroy, H. L. and Chowdhury, M. A. (1987) Com earworm (Lepidoptera: Noctuidae): Effects of substerilizing doses of radiation and inherited sterility on reproduction. J. econ. entomol. 80, 483–89.CrossRefGoogle Scholar
Duncan, D.B. (1955) Multiple range and multiple F tests. Biometrics 11, 1–42.CrossRefGoogle Scholar
Hussain, A.A. (1974) Date Palms and Dates with their Pests in Iraq. Baghdad Univ. Press.Google Scholar
Hussain, A.A. (1985) Date Palms and Dates with their Pests in Iraq. Basrah Univ. Press.Google Scholar
Husseiny, M. and Madsen, H.F. (1964) Sterilization of the navel orangeworm, Paramyelais transitella (Walk.) by gamma radiation, (Lepidoptera: Phycitidae). Hilgardia 36, 113–137.CrossRefGoogle Scholar
LaChance, L.E. (1984) Genetic methods for the control of Lepidopteran pests: Status and potential. F1 Sterility for Control of Lepidoptera Pests (Report Consultants meeting, Vienna, 1984). IAEA, Vienna.Google Scholar
Li, Y.Y., Zhang, H.Q., Lou, H.Z. and Zhao, C.D. (1988) The inherited sterility of the corn borer, Ostrinia furnacalis (Guen). Modern Insect Control: Nuclear Techniques and Biotechnology (Proc. Symp. Vienna, 1987) IAEA, Vienna. pp. 403–411.Google Scholar
North, D.T. (1975) Inherited sterility in Lepidoptera. A. Rev. Entomol. 20, 167–182.CrossRefGoogle ScholarPubMed
North, D.T. and Holt, G.G. (1968) Genetic and cytogenetic basis of radiation-induced sterility in the adult male cabbage looper, Trichoplusia ni. In Isotopes and radiation in entomology. International Atomic Energy Agency Symposium, Vienna. pp. 233–247.Google Scholar
Proshold, F. I. and Bartell, J. A. (1970) Inherited sterility in progeny of irradiated male tobacco budworms: Effects on reproduction, developmental time and sex ratio. J. econ. Entomol. 63, 280–285.CrossRefGoogle Scholar
Proshold, F.I. and Bartell, J. A. (1972) Differences in radiosensitivity of two colonies of tobacco budworm, Heliothis virescens. Can. Entomol. 104, 995–1002.CrossRefGoogle Scholar
Proverbs, M. D. (1962) Progress on the use of sexual sterility for control of the codling moth, Carpocapsa pomonella (L.) (Lepidoptera: Olethreutidae). Proc. Entomol. Soc. Ont. 92, 5–11.Google Scholar
Walfenbarger, D.A. and Guerra, A.A. (1971) Response of strains and sexes of the tobacco budworm to gamma radiation. J. econ. Entomol. 644, 1412–1415.CrossRefGoogle Scholar