Influence of Chilling Duration on Oxygen Consumption and Hatchability in Eggs of the Silkworm, Bombyx mori

  • Yoon, Hyung-Joo (Department of Agricultural Biology, The National Institute of Agricultural Science & Technology, RDA) ;
  • Kim, Sam-Eun (Department of Agricultural Biology, The National Institute of Agricultural Science & Technology, RDA) ;
  • Kim, Jong-Gill (Department of Agricultural Biology, The National Institute of Agricultural Science & Technology, RDA) ;
  • Park, Ji-Young (Department of Agricultural Biology, The National Institute of Agricultural Science & Technology, RDA)
  • Published : 2004.03.01

Abstract

The rate of oxygen consumption of the silkworm eggs was measured to set up the barometer for measuring the effect of egg chilling on diapause termination. In diapause eggs, $O_2$ uptake showed a maximum of 79.2 ${mu}ell$/mg eggs/hr, at one day after oviposition and then gradually decreased to 2.2${mu}ell$/mg eggs/hr at 9days. The rates of oxygen uptake of eggs raised immediately after HCl-treatment and reached to a maximal level of 484.5 ${mu}ell$/mg eggs/hr in 9-day-old eggs, which corresponds to 220 fold that of diapause eggs, and the hatching ability was also over 50%. In order to break diapause, eggs incubated at $25^{\circ}C$ for 30 days after oviposition had to be kept at least for 45 days at 5$^{\circ}C$, but chilled eggs for 90 days or longer hatched at 10 days as normal hatching periods. We also investigate periods which the value of $O_2$ uptake of eggs chilled during 15 to 120 days at 5$^{\circ}C$ reached at 200 ${mu}ell$/mg eggs/hr. As a result of that, $O_2$ uptake of eggs chilled during 15 to 45days were not reached at 200 ${mu}ell$/mg eggs/hr and longer the chilling durations are, the higher the rate of $O_2$ uptake is and the longer the chilling durations are, the shorter the periods up to hatching is. And also, hatch-ability increased rapidly as $O_2$ uptake reaches over 20/eggs/hr.

Keywords

References

  1. Braune, H. J. (1976) Effects of temperature on the rates of oxygen consumption during morphogenesis and diapause in the egg stage of Leptopterna dolobrata (Heteroptea: Miridae). Oecologia 25, 77-87 https://doi.org/10.1007/BF00345035
  2. Chino, H. (1958) Carbohydrate metabolism in the diapause egg of the silkworm, Bombyx mori. II. Conversion of glycogen into sorbitol and glycerol during diapause. J. Insect Physiol. 2, 1-2 https://doi.org/10.1016/0022-1910(58)90024-6
  3. Crozier, A. J. G. (1979) Supradian and infrandian cycle in oxygen uptake of diapausing pupae of Pieris brassicae. J. Insect Physiol. 25, 575-582 https://doi.org/10.1016/0022-1910(79)90072-6
  4. Denlinger, D. L., J. H. Wellis and G. Fraenkel (1972) Rates and cycles of oxygen consumption during pupal diapause in Sarcophaga flesh flies. J. Insect Physiol. 18, 871-882 https://doi.org/10.1016/0022-1910(72)90026-1
  5. Ellingsen, I. J. (1978) Oxygen consumption in active and quiescent protonymphs of the American house-dust mite. J. Insect Physiol. 24, 13-16 https://doi.org/10.1016/0022-1910(78)90005-7
  6. Furusawa, T., M. Shikata and O. Yamashita (1982) Temperature dependent sorbitol utilization in diapause eggs of the silkworm, Bombyx mori. J. Compo Physiol. B 147, 21-26
  7. Fukuda, S. (1951) The production of the diapause eggs by transplanting the suboesophageal ganglion in the silkworm, Bombyx mori L., with special reference to the organs concerning determination of voltinism (A preliminary note). Proc. Japan Acad. 27, 667-671
  8. Hasegawa, K. (1951) Studies on the voltinism in the silkworm, The production of the diapause eggs by transplanting the suboesophageal ganglion in the silkworm, Bombyx mori. Proc. Japan Acad. 27, 672-677
  9. Kai, H. (1983) Attempts to elucidate insect diapause development characterized by the potentiation of physiological development during exposure to low temperature. J. Seric. Sci. Jpn 52, 283-289
  10. Kai, H., K. Kawashiri, S. Nakashima and M. Azuma (1995) Fixed minimum duration of chilling critical to the termination of diapause, and effects of longer chilling on hatching mode in eggs of Bombyx mori. J. Seric. Sci. Jpn 64, 132-141
  11. Kim, S. (1987) Changes in eggshell permeability to oxygen during the early developmental stages in diapause eggs of the silkworm, Bombyx mori. J. Insect Physiol. 33, 229-235 https://doi.org/10.1016/0022-1910(87)90042-4
  12. Kitazawa, T., T Kanda and T. Takami (1963) Cabohydarte metabolism in the silkworm egg in relation to diapause. Bull. Seric. Exp. Stn. Jpn 18, 283-295
  13. May, M. L. (1989) Oxygen consumption by adult colorado potato beetle, Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae). 1. Insect Physiol. 35, 797-804 https://doi.org/10.1016/0022-1910(89)90138-8
  14. Miya, K. (1984) Early embryogenesis Bombyx mori; in Insect Ultrastructure. Vol. 2, King, R. C. and H. Akai (eds.), pp. 49-73, Plenum Press, New York
  15. Okada, M. (1971) Role of the chorion as a barrier to oxygen in the diapause of the silkworm, Bombyx mori L. Experientia 27, 658-660 https://doi.org/10.1007/BF02136945
  16. Scheniderman, H. A. and C. M. Williams (1953) The physiology of insect diapause VII. The respiratory metabolism of the Cecropia silkworm, during diapause and development. Biol. Bull. 105, 320-334 https://doi.org/10.2307/1538648
  17. Sonobe, H., H. Hyyama, and H. Keino (1977) Changes in the amount of the diapause factor in the subesophageal ganglion during development of the silkworm, Bombyx mori. J. Insect Physiol. 23, 633-637 https://doi.org/10.1016/0022-1910(77)90059-2
  18. Sonobe, H., A. Matsymoto, Y. Fukuzaki and S. Fujiwara (1979) Carbohydrate metabolism and restricted oxygen supply in the eggs of the silkworm, Bombyx mori. J. Insect Physiol. 25, 381-388 https://doi.org/10.1016/0022-1910(79)90003-9
  19. Sonobe, H. and M. Nakamura (1991) A re-investigation of the oxygen permeability of the chorion in relation to the onset of embryonic diapause of the silkworm, Bombyx mori. J. Insect Physiol. 37, 727-732 https://doi.org/10.1016/0022-1910(91)90106-A
  20. Sonobe, H. and Y. Okada (1984) Studies on embryonic diapause in the pnd mutant of the silkworm, Bombyx mori L. III. Accumulation of alanine in the diapause eggs. Rouxs Arch. Develop. Biol. 193, 414-417 https://doi.org/10.1007/BF00848233
  21. Takesue, S., H. Keino and K. Onitake (1980) Blastoderm formation in the silkworm egg (Bombyx mori). J. Embryo. Exp. Morphol. 60, 117-124
  22. Waku, Y. (1965) Oxygen consumption during diapause in the Lepidopterous pupae-Physiological and autecological significance of its U shaped curve. Sci. Rep. Tohoku Univ. 28, 298-314
  23. Yaginuma, T. and O. Yamashita (1986) Malate-aspartate cycles as an effective hydrogen shuttle at the termination of diapause in the eggs of Bombyx mori. J. Insect Physiol. 16, 677-685
  24. Yaginuma, T. and O. Yamashita (1999) Oxygen consumption in relation to sorbitol utilization at the termination of diapause eggs of the silkworm, Bombyx mori. J. Insect Physiol. 45, 621-627 https://doi.org/10.1016/S0022-1910(98)00150-4