Skip to main content
Log in

Sex determination in the genus Oreochromis

2. Sex reversal, hybridisation, gynogenesis and triploidy in O. aureus Steindachner

  • Originals
  • Published:
Theoretical and Applied Genetics Aims and scope Submit manuscript

Summary

Sex ratios from 62 single-pair matings of normal broodstock O. aureus were highly heterogeneous with an overall deficit of males (41.4%). Peaks in the sex ratio frequency distribution occurred at 1∶1, 3∶5 and 1∶3 (male∶female). Hybridisation of O. aureus with O. mossambicus, O. spilums and O. niloticus produced highly variable sex ratios, suggesting a complexity of hybrid sex determination. Few valid inferences could be made regarding intraspecific sex determination from these hybrid data. Sex ratios from progeny testing of sex-reversed males (1∶3) and most sex-reversed females (1∶0) provide evidence for female heterogamety in O. aureus. Several aberrant ratios observed suggest Mendelian inheritance of an autosomal recessive gene (F,f), epistatic to the major sex-determining gene (W,Z). Sex ratios of triploids and gynogens support the hypothesis of recombination between the centromere and the major sex-determining locus. Progeny testing of a female mitogyne demonstrated the viability of a novel WW “superfemale”, which gave only female offspring. Not all data could be explained by a two-factor model of sex determination. Further exceptional sex ratios may be accounted for by rare autosomal or environmental sex-modifying factors. It is concluded that O. aureus has a multifactorial mechanism of sex determination with the underlying primary mechanism of female heterogamety.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Avtalion RR, Hammerman IS (1978) Sex-determination in Sarotherodon (Tilapia). 1. Introduction to the theory of autosomal influences. Bamidgeh 30:110–115

    Google Scholar 

  • Bull JJ (1983) Evolution of sex-determining mechanisms. Benjamin/Cummings, Menlo Park/CA

    Google Scholar 

  • Chen FY (1969) Preliminary studies on the sex-determining mechanism of Tilapia mossambica Peters and T. hornorum Trewavas. Verh Int Verh Limnol 17:719–724

    Google Scholar 

  • Colombelli B, Thiébaud ChH, Müller WP (1984) Production of WW super females by diploid gynogenesis in Xenopus laevis. Mol Gen Genet 194:57–59

    Google Scholar 

  • Fishelson L (1962) Hybrids of two species of fishes of the genus Tilapia (Cichlidae, Teleostei). Fishermans' Bull 4(2): 14–19

    Google Scholar 

  • Guerrero RD (1975) Use of androgens for the production of all-male Tilapia aurea (Steindachner). Trans Am Fish Soc 104:342–348

    Google Scholar 

  • Guerrero RD, Shelton WL (1974) An aceto-carmine squash method for sexing of juvenile fishes. Prog Fish Cult 36:56

    Google Scholar 

  • Hammerman IS, Avtalion RR (1979) Sex-determination in Sarotherodon (Tilapia). 2. The sex-ratio as a tool for the determination of genotype-a model of autosomal influence. Theor Appl Genet 55:177–187

    Google Scholar 

  • Hopkins KD (1977) Sex reversal of genotypic male Sarotherodon aureus (Cichlidae). MS thesis. Auburn University, Alabama

    Google Scholar 

  • Hopkins KD (1979) Production of monosex tilapia fry by breeding sex-reversed fish. PhD thesis Auburn University, Alabama

    Google Scholar 

  • Hopkins KD, Shelton WL, Engle CR (1979) Estrogen sex-reversal of Tilapia aurea. Aquaculture 18:263–268

    Google Scholar 

  • Hsiao SM (1980) Hybridization of Tilapia mossambica, T. nilotica, T. aurea and T. zillii — a preliminary report. China Fisheries Monthly Taipei 332:3–13

    Google Scholar 

  • Hulata G, Wohlfarth G, Rothbard S (1983) Progeny-testing selection of tilapia broodstocks producing all-male hybrid progenies -preliminary results. Aquaculture 33:263–268

    Google Scholar 

  • Jalabert B, Kammacher P, Lessent P (1971) Determinism du sexe chez les hybrides entre Tilapia macrochir et T. nilotica. Etude de la sex-ratio dans les recroisements des hybrides de première génération par les espèces parentes. Ann Biol Anim Biochim Biophys 11:155–165

    Google Scholar 

  • Liu C-Y (1977) Aspects of reproduction and progeny testing in Sarotherodon aureus (Steindachner). MS thesis, Auburn University, Alabama

    Google Scholar 

  • Mair GC (1988) Studies on sex-determining mechanisms in Oreochromis species. PhD thesis, University College of Swansea, Wales

    Google Scholar 

  • Mair GC, Penman DJ, Scott A, Skibinski DOR Beardmore JA (1987a) Hormonal sex reversal and the mechanisms of sex determination in Oreochromis. In: Tiews K (ed) Proc World Symp Selection, Hybridization and Genetic Engineering in Aquaculture, vol II, Bordeaux, May 27–30, 1986, pp 289–300

  • Mair GC, Scott A, Beardmore JA, Skibinski DOF (1987b) A technique for the induction of diploid gynogenesis in Oreochromis niloticus by the suppression of the first mitotic division. In: Tiews K (ed) Proc World Symp Selection, Hybridization, and Genetic Engineering in Aquaculture, vol II, Bordeaux, May 27–30, 1986, pp 301–312

  • Mair GC, Beardmore JA, Skibinski DOF (1990) Experimental evidence for environmental sex determination in Oreochromis species. In: Hirano R, Hanyu I (eds) Proc 2nd Asian Fisheries Forum, Tokyo, April 17–22,1989. Asian Fisheries Society, Manila, The Philippines, pp 555–558

    Google Scholar 

  • Mair GC, Scott AG, Penman DJ, Bearmore JA, Skibinski DOF (1991) Sex determination in the genus Oreochromis. 1. Sex reversal, gynogenesis and triploidy in O. niloticus (L.) Theor Appl Genet 82:144–152

    Google Scholar 

  • Majumdar KD, McAndrew BJ (1983) Sex-ratios from inter-specific crosses within the tilapias. In: Fishelson L, Yaron Z (eds) Proc Int Symp Tilapia in Aquaculture, May 1983, Nazareth, Israel, pp 261–269

    Google Scholar 

  • Mires D (1977) Theoretical and practical aspects of the production of all-male Tilapia hybrids. Bamidgeh 29:94–101

    Google Scholar 

  • Nass CAG (1959) The Chi-squared test for small expectations in contingency tables, with special reference to accidents and absenteeism. Biometrika 46:365–385

    Google Scholar 

  • Penman DJ (1989) Genetic approaches to the improvement of Oreochromis species. PhD thesis, University College of Swansea, Wales

    Google Scholar 

  • Penman DJ, Shah MS, Beardmore JA, Skibinski DOF (1987) Sex ratio of gynogenetic and triploid tilapia. In: Tiews K (ed) Proc World Symp Selection, Hybridization, and Genetic Engineering in Aquaculture, vol II, Bordeaux, May 27–30, 1986, pp 267–276

  • Pruginin Y, Rothbard S, Wohlfarth G, Holavy A, Moav R, Hulata G (1975) All-male broods of Tilapia nilotica and T. aurea hybrids. Aquaculture 6:11–21

    Google Scholar 

  • Sanico AF (1975) Effects of 17α-ethynyltestosterone and estrone on the sex ratio and growth of Tilapia aurea (Steindachner). MS thesis, Auburn University, Alabama

    Google Scholar 

  • Shelton WL, Rodriguez-Guerrero D, Lopez-Macias J (1981) Factors affecting androgen sex-reversal of Tilapia aurea. Aquaculture 25:59–65

    Google Scholar 

  • Shelton WL, Meriwether FH, Semmens KJ, Calhoun WE (1983) Progeny sex-ratios from intraspecific pair spawnings of Tilapia aurea and T. nilotica. In: Fishelson L, Yaron Z (eds) Proc Int Symp Tilapia in Aquaculture, May 1983, Nazareth, Israel, pp 270–280

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by K. Sittmann

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mair, G.C., Scott, A.G., Penman, D.J. et al. Sex determination in the genus Oreochromis . Theoret. Appl. Genetics 82, 153–160 (1991). https://doi.org/10.1007/BF00226206

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00226206

Key words

Navigation