Register      Login
Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Distribution of spermatozoa in the outer perivitelline layer from above the germinal disc of emu and ostrich eggs

Irek A. Malecki A B and Graeme B. Martin A
+ Author Affiliations
- Author Affiliations

A School of Animal Biology, Faculty of Natural and Agricultural Sciences, The University of Western Australia, Crawley, WA 6009, Australia.

B To whom correspondence should be addressed. email: imalecki@agric.uwa.edu.au

Reproduction, Fertility and Development 15(5) 263-268 https://doi.org/10.1071/RD02080
Submitted: 24 September 2002  Accepted: 4 July 2003   Published: 16 October 2003

Abstract

In the present study, we determined the distribution of spermatozoa in the perivitelline layer above the germinal disc (GD) of emu and ostrich eggs that had been laid at random intervals after mating. Eggs were opened, the perivitelline layer overlying the GD region was collected and sperm were visualized with 4′,6′-diamidino-2-phenylindole under a fluorescence microscope. To map the distribution of sperm, the GD was divided into six areas (A–F), with A being the centre of the GD and F the area furthest from the centre. In both species, more spermatozoa were found in areas B, C and D than in areas A, E and F. More than half the GD spermatozoa were found in areas B, C and D. The pattern of distribution of spermatozoa across the GD depended on the total number of sperm in the GD. In the emu, the pattern was related to delay since last copulation and time of laying, whereas in the ostrich the pattern was related to the month of the season and the sex ratio of the mating system. When the total number of spermatozoa in the GD increased, the number of spermatozoa increased in every area of the GD, but the centre and the outer areas were the least affected. We conclude that sperm numbers are highest in a band immediately around the centre of the GD and then decline with increasing distance from the centre. The low numbers in the centre of the GD may be due to either low attractiveness of the centre for sperm or high attractiveness of the area immediately adjacent to the centre.

Extra keywords: fertilization


Acknowledgments

We thank John Koppen and Peter Cowl for their skilful technical assistance. The Rural Industries Research & Development Corporation (Project No. UWA-52A) funded this work.


References

Bakst, M. R. (1978). Scanning electron microscopy of the vitelline membrane of the hen ovum. J. Reprod. Fertil. 52, 361–4.
PubMed |

Bakst, M. R. , and Howarth, B. (1977a). Hydrolysis of the hen’s perivitelline layer by cock sperm. Biol. Reprod. 17, 370–9.
PubMed |

Bakst, M. R. , and Howarth, B. (1977b). The fine structure of the hen’s ovum at ovulation. Biol. Reprod. 17, 361–9.
PubMed |

Birkhead, T. R. , Pellatt, E. J. , and Fletcher, F. (1993). Selection and utilization of spermatozoa in the reproductive tract of the female zebra finch Taeniopygia guttata.  J. Reprod. Fertil. 99, 593–600.
PubMed |

Birkhead, T. R. , Sheldon, B. C. , and Fletcher, F. (1994). A comparative study of sperm : egg interaction in birds. J. Reprod. Fertil. 101, 353–61.
PubMed |

Bramwell, R. K. , and Howarth, B. (1992). Preferential attachment of cock spermatozoa to the perivitelline layer directly over the germinal disc of the hen’s ovum. Biol. Reprod. 47, 1113–17.
PubMed |

Bramwell, R. K. , Marks, H. L. , and Howarth, B. (1995). Quantitative determination of spermatozoa penetration of the perivitelline layer of the hen’s ovum as assessed on the oviposited eggs. Poult. Sci. 74, 1875–83.
PubMed |

Bramwell, R. K. , Howarth, B. , Geurts, L. M. , and Graham, J. K. (1997). Effect of low or high sperm penetration values at the germinal disc on early embryonic mortality in chicken eggs. Poult. Sci. 76, 388.(Abstract)


Fofanova, K. V. (1965). Morphological data on polyspermy in chickens. Fed. Proc. Transl. Suppl. 24, T239–T47.


Ho, J. J. , and Meizel, S. (1976). Hydrolysis of the hen egg vitelline membrane by cock sperm acrosin and other enzymes. J. Exp. Zool. 194, 429–38.


Howarth, B. , and Digby, S. T. (1973). Evidence for penetration of the vitelline membrane of the hen’s ovum by a trypsin like acrosomal enzyme. J. Reprod. Fertil. 33, 123–5.
PubMed |

Malecki, I. A. , and Martin, G. B. (2002). Fertility of the male and female emus (Dromaius novaehollandiae) as determined by spermatozoa trapped in eggs. Reprod. Fertil. Dev. 14, 495–502.
PubMed |

Malecki, I. A. , and Martin, G. B. (2003). Sperm supply and egg fertilisation in the ostrich (Struthio camelus). Reprod. Dom. Anim. ,(in press).
Crossref | GoogleScholarGoogle Scholar |

Malecki, I. A. , Martin, G. B. , and Lindsay, D. R. (1997). Semen production in the emu (Dromaius novaehollandiae) 2. Effect of collection frequency on the production of semen and spermatozoa. Poult. Sci. 76, 622–6.
PubMed |

Okamura, F. , and Nishiyama, H. (1978). The passage of spermatozoa through the vitelline membrane in the domestic fowl Gallus gallus.  Cell Tissue Res. 188, 497–508.
PubMed |

Olsen, M. W. , and Fraps, R. M. (1944). Maturation, fertilization and early cleavage of the egg of the domestic turkey. J. Morphol. 74, 297–309.


Olsen, M. W. , and Nehrer, B. H. (1948). The site of fertilization in the domestic fowl. J. Exp. Zool. 109, 355–66.


Perry, M. M. (1987). Nuclear events from fertilization to the early cleavage stages in the domestic fowl (Gallus domesticus). J. Anat. 150, 99–109.
PubMed |

Perry, M. M. , Gilbert, A. B. , and Evans, A. J. (1978). The structure of the germinal disc region of the hen’s ovarian follicle during the rapid growth phase. J. Anat. 127, 379–92.
PubMed |

Romanoff, A. L., and  Romanoff, A. J. (1949). ‘The Avian Egg.’ (John Wiley & Sons: New York.)

Steele, M. G. , Meldrum, W. , Brillard, J.-P. , and Wishart, G. J. (1994). The interaction of avian spermatozoa with the perivitelline layer in vitro and in vivo.  J. Reprod. Fertil. 101, 599–603.
PubMed |

Stepinska, U. , and Olszanska, B. (2001). Detection of deoxyribonuclease I and II activities in Japanese quail oocytes. Zygote 9, 1–7.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Van Krey, H. , Ogasawara, F. , and Lorenz, F. (1966). Distribution of spermatozoa in the oviduct and fertility in domestic birds. IV. Fertility of spermatozoa from the infundibular and uterovaginal glands. J.Reprod. Fertil. 11, 257–62.
PubMed |

Waddington, D. , Gribbin, C. , Sterling, R. J. , Sang, H. , and Perry, M. M. (1998). Chronology of events in the first cell cycle of the polyspermic egg of the domestic fowl (Gallus domesticus). Int. J. Dev. Biol. 42, 625–8.
PubMed |

Wishart, G. J. (1987). Regulation of the length of the fertile period in the domestic fowl by numbers of oviducal spermatozoa, as reflected by those trapped in laid eggs. J. Reprod. Fertil. 80, 493–8.
PubMed |

Wishart, G. J. (1997). Quantitative aspects of sperm : egg interaction in chickens and turkeys. Anim. Reprod. Sci. 48, 81–92.
Crossref | GoogleScholarGoogle Scholar | PubMed |