Preservation of gametes
In many species, the maturation of gonads in the two sexes is not
synchronous. Males often show testicular recrudescence earlier during the
season. Because of this, ripe males occur during the beginning of the season,
when the females are not yet mature and ready for spawning. The reverse
situation occurs during the end of the breeding season. Under such
circumstances, it will be most advantageous to have a suitable means of
preserving the gametes for artificial fertilization, when needed. Methods of
gamete preservation would also help in the initiation of genetic selection
programmes, by providing easy access to a reserve of genetic material of known
and desired qualities.
Cryopreservation with liquid nitrogen, used widely in the preservation
of cattle and live-stock sperm, has been tried for the preservation of a number
of species of fish. Blaxter (1955) reported successful fertilization of fresh
eggs with cryopreserved (-79°C) sperm of Clupeaharengus.
Sections of ripe testis were stored in80 per cent sea water containing 12.5 per
cent glycerol as a protector, and the mixture frozen quickly or slowly at
1°C/min to -30°C, then quickly to -79°C (using dry ice). Besides the sperm of
rainbow trout, spermatozoa of the common carp, Chinese and Indian carps and
grey mullet are among the cultivated species which have been subjected to
cryopreservation, which consists of cooling and storing at subzero temperatures
of liquid nitrogen (-196°C), using dimethyl sulphoxide, glycerine, ethyl glycol
or other cryoprotectants and diluents (Harvey and Hoar, 1979). Attempts at
cryopreservation of ova have not been as successful as for sperm. Zell (1978)
reported the first successful cryopreservation of unfertilized ova and zygotes
of salmonid fish. Ova frozen in liquid nitrogen at -20°C for five minutes
proved to be fertile, and zygotes frozen at -50°C survived the exposure. All
subsequent attempts have failed. While it is difficult to predict possible
advances in cryopreservation of fish gametes, it would appear that the results
so far indicate only the feasibility of short-term preservation of semen or the
prolongation of embryonation.
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