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Cryopreservation of carp (Cyprinus carpio) blastomeres

Published online by Cambridge University Press:  15 January 1999

Silvia Leveroni Calvi
Affiliation:
Dipartimento di Scienze Zootecniche, Università degli Studi di Torino, Torino, Italy Station commune de recherches en ichtyophysiologie, biodiversité et environnement, Équipe ‘Ichtyodiversité & cryoconservation’, Inra, Campus de Beaulieu, 35042 Rennes cedex, France
Gérard Maisse
Affiliation:
Station commune de recherches en ichtyophysiologie, biodiversité et environnement, Équipe ‘Ichtyodiversité & cryoconservation’, Inra, Campus de Beaulieu, 35042 Rennes cedex, France
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Abstract

The technique already adopted by the authors for the cryopreservation of rainbow trout blastomeres was applied to carp. Three stages were utilised for cell freezing: the morula stage, the early blastula stage and the late blastula stage. Survival rates were 89 ± 1.6 % for morula cells, 94 ± 0.6 % for early blastula cells and 96 ± 0.4 % for late blastula cells. Early blastula and late blastula cells reaggregated into morula-like bodies within 2 h in culture medium. Results suggest that the freezing technique adopted for rainbow trout may be successfully applied to carp. The morula stage blastomeres were more sensitive to freezing than blastula stage blastomeres, as already found in rainbow trout.

Type
Research Article
Copyright
© Elsevier, Inra, Ifremer, Cemagref, Ird, Cnrs, 1999

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