Open Access Open Access  Restricted Access Subscription Access

Cryopreservation of Carp Spermatozoa


Affiliations
1 Department of Fisheries Biology and Resource Management, Fisheries College & Research Institute, Thoothukudi – 628008, Tamil Nadu, India
 

A successful cryopreservation method would offer many advantages to an aquaculturist. Cryopreservation can provide a year round supply of seeds from desired species regardless of the spawning season and allow hybridization, greater ease in carrying out selective breeding and stock improvement. Studies were conducted on cryopreservation of spermatozoa from Indian major carps. Effect of different concentration of glycerol and equilibration periods on the post thaw motility of spermatozoa from Catla, Rohu and Mrigal were observed. The maximum motility (80 - 85%) was observed with the equilibration period of 20 - 40 minutes with the concentration of 10-15% of glycerol. Rohu showed the same trend with the maximum motility of 78-87%. In Mrigal maximum motility (85-88%) was observed with the equilibration time of (20-40 minutes) with the concentration of glycerol in between (10-15%). Like glycerol, the same type of experiment was conducted with Dimethyl sulphoxide (DMSO). Post thaw motility of cryopreserved spermatozoa in DMSO showed the same way as glycerol. Apart from the above, percentage of motility of spermatozoa was observed with respect to different thawing temperatures. Maximum motility was observed at the thawing temperature of 40oC in catla (85%), Rohu (80.00%) and Mrigal (83%). Interesting results were obtained from the fertilization studies of cryopreserved spermatozoa of Catla with the eggs from the matured Catla breeders. Fertilization rate of 75-80% and the hatching rate of 60% was observed from the above study. From the above results, it could be possible to use cryopreserved spermatozoa for commercial production of fish seeds in fish hatcheries.

Keywords

Cryopreservation, Catla, Rohu, Mirgal, DMSO, Fertilization Rate
User

  • Baynes S M, and Scott A P (1987). Cryopreservation of rainbow trout spermatozoa: The influence of sperm quality, egg quality and extender composition on post-thaw fertility, Aquaculture, vol 66, 53-67.
  • Billard R (1980). Prolongation de la duree de motilite et du pouvoir fecondant des spermatozoids de Truite arc-en-ciel par addition de thephylline au milieu de dilution, C. R. Academic Science, Paris, vol 291, D, 649-652.
  • Blaxter J H S (1953). Sperm storage and cross-fertilization of spring and autumn spawning herring, Nature (London), vol 172(4391), 1189-1190.
  • Bolla S, Holmefjord I et al. (1987). Cryogenic preservation of Atlantic halibut sperm. Aquaculture, vol 65(3-4), 371-374.
  • Chao N H, Chao W C et al. (1986). The biological properties of black porgy (Acanthopagrus schlegeli) sperm and its cryopreservation, Proceedings of National Science Council, B. Taiwan, vol 10(2), 145-149.
  • Chao N H, Chao W C et al. (1987). The properties of tilapia sperm and its cryopreservation, Journal of Fish Biology, vol 30(2), 107-119.
  • Chao N H, Tsai H P, and Liao I C (1992) Short and Long-term cryopreservation of sperm and sperm suspension of the grouper, Epinephelus malabaricus (Bloch and Schnaider), Asian Fisheries Science, vol 5, 103-116.
  • Chen S L, Liu X T et al. (1992). Cryopreservation of spermatozoa of silver carp, common carp, blunt snout bream and grass carp, Acta Zoologica sínica, vol 38, 413-424.
  • Cognie F, Billard R et al. (1989). La cryopreservation de la laitance de la carpe, Cyprinus carpio, Journal of Applied Ichthyology, vol 5(4), 165-176.
  • Erdahl D A, and Graham E F (1978). Cryopreservation of salmonid spermatozoa, Cryobiology, vol 15, 362-364.
  • Guest W C, Avault J W Jr et al. (1976). Preservation of channel catfish sperm, Transaction American, Fisheries Society, vol 105, 469-474.
  • Gwo J C (1993). Cryopreservation of black grouper (Epinephelus malabaricus) spermatozoa, Theriogenology, vol 39(6), 1331-1342.
  • Gwo J C, Kurokura H et al. (1993). Cryopreservation of spermatozoa from rainbow trout, common carp and marine puffer, Bulletin of Japan Social Science Fish, vol 59(5), 777-782.
  • Gwo J C, Strawn K et al. (1991). Cryopreservation of Atlantic croaker spermatozoa, Aquaculture, vol 94(4), 355-375.
  • Harvey B (1983). Cryopreservation of Sarotherodon mossambicus spermatozoa, Aquaculture, vol 32, 313-320.
  • Harvey B, Kelley R N et al. (1982). Cryopreservation of Zebra fish spermatozoa using methanol, Canadian Journal of Zoology, vol 60(8), 1867-1870.
  • Edwin M J, and Ulaganathan V (1988). Deep freezing of semen, Tamil Nadu Agriculture University, Coimbatore, vol 46.
  • Kumar K (1989). Studies on cryogenic preservation of carp spermatozoa, Das P, Jhingran A G (Ed), Fish Genetics in India, Today and Tomorrow’s Printers and Publishers, New Delhi, 199-206.
  • Lahnsteiner F, Wiesmann T et al. (1992). Fine structural changes in spermatozoa of the grayling, Thymallus thymallus (Pisces: Teleostei), during routine cryopreservation. Aquaculture, vol 103(1), 73-84.
  • Lakra W S, (1992). Fish gamete and embryo cryopreservation research in India, Billard R (Ed.), Workshop of Gamete and embryo storage and cryopreservation in Aquatic organisms, France, 16.
  • Legendre M, and Billard R (1980). Cryopreservation of rainbow trout sperm by deep-freezing, Reproduction, Nutrition, Development, vol 20, No 6, 1859-1868.
  • Linhart O, Liehman P et al. (1992). Long term preservation of common carp (Cyprinus carpio L) spermatozoa, Billard R (Ed.), Workshop on gamete and embryo storage and cryopreservation in aquatic organisms, France, 40.
  • Mazur P (1977), The role of intracellular freezing in the death of cells cooled at supraoptimal rates, Cryobiology,vol 14, 251-272.
  • Moczarski M (1976). Cryobiological factors in grass carp sperm preservation, 8th Proceeding International Congress Animal Reproduction, 1030-1033.
  • Ott A G, and Horton H F (1971a). Fertilization of Chinook and coho salmon eggs with cryopreserved sperm, Journal of Fish Research Canada, vol 28(5), 745-748.
  • Ott A G, and Horton H F (1971b). Fertilization of steel head trout (Salmo gairdneri) eggs with cryopreserved sperm, Journal of Fish Research Board Canada, vol 28(12), 1915-1918.
  • Piironen J, and Hyvarinen H (1983). Cryopreservation of spermatozoa of the whitefish, Coregonus muskun pallas, Journal of Fish Biology, vol 22(2), 159-163.
  • Piironen J (1993). Cryopreservation of sperm from brown trout (Salmo trutta lacustris L.) and Arctic charr (Salvelinus alpines L.), Aquaculture, vol 116 (2-3), 275-285.
  • Polge C, Smith A U et al. (1949). Revival of spermatozoa after vitrification and dehydration at low temperature, Nature, vol 164, 666-666.
  • Scott A P, and Baynes S M (1980). A review of the biology handling and storage of salmonid spermatozoa, Journal of Fish Biology, vol 17, 707-739.
  • Snedecor G W, and Cochran W G (1976). Statistical methods, Oxford and IBH publishing Co, 593.
  • Steyn G J, Van vuren J H J et al. (1985). Preliminary investigations on the cryopreservation of Clarias gariepinus (Clariidae : Pisces) sperm, Water, S.A, vol 11(1), 15-18.
  • Stoss J, and Donaldson E M (1982). Preservation of fish gametes. Richter C J J and Goos H J T (Eds.), Preccedings of International symposium on reproducyive physiology of fish, Wageningen, The Netherlands, 114-122.
  • Stoss J, and Holtz W (1981a). Cryopreservation of rainbow trout (Salmo gairdneri) sperm, I. Effects of thawing solution, sperm density and interval between thawing and insemination, Aquaculture, vol 22, 97-104.
  • Stoss J, and Holtz W (1983a). Cryopreservation of rainbow trout (Salmon Gairdneri) sperm, III Effect of proteins in the diluent, sperm from different males and internal between sperm collection and freezing, Aquaculture, vol 31, 275-282.
  • Stoss J, and Holtz W (1983b). Cryopreservation of rainbow trout (Salmo gairdneri) sperm, IV. The effect of DMSO concentration and equilibration time on sperm survival, sucrose and KCl as extender components and the osmolality of the thawing solution, Aquaculture, vol 32(3-4), 321-330.
  • Stoss J (1983). Fish gamete preservation and spermatozoan physiology, Hoar W S, Randall D J, and Donaldson E M (Eds.), Fish Physiology, Academic Press, New York, vol IX B, 305-350.
  • Terner C (1986). Evaluation of salmonid sperm motility for cryopreservation, The Progressive Fish-Culturist, vol 48(3), 230-232.

Abstract Views: 519

PDF Views: 0




  • Cryopreservation of Carp Spermatozoa

Abstract Views: 519  |  PDF Views: 0

Authors

T. Francis
Department of Fisheries Biology and Resource Management, Fisheries College & Research Institute, Thoothukudi – 628008, Tamil Nadu, India
C. Archana Devi
Department of Fisheries Biology and Resource Management, Fisheries College & Research Institute, Thoothukudi – 628008, Tamil Nadu, India
M. Selvamagheswaran
Department of Fisheries Biology and Resource Management, Fisheries College & Research Institute, Thoothukudi – 628008, Tamil Nadu, India

Abstract


A successful cryopreservation method would offer many advantages to an aquaculturist. Cryopreservation can provide a year round supply of seeds from desired species regardless of the spawning season and allow hybridization, greater ease in carrying out selective breeding and stock improvement. Studies were conducted on cryopreservation of spermatozoa from Indian major carps. Effect of different concentration of glycerol and equilibration periods on the post thaw motility of spermatozoa from Catla, Rohu and Mrigal were observed. The maximum motility (80 - 85%) was observed with the equilibration period of 20 - 40 minutes with the concentration of 10-15% of glycerol. Rohu showed the same trend with the maximum motility of 78-87%. In Mrigal maximum motility (85-88%) was observed with the equilibration time of (20-40 minutes) with the concentration of glycerol in between (10-15%). Like glycerol, the same type of experiment was conducted with Dimethyl sulphoxide (DMSO). Post thaw motility of cryopreserved spermatozoa in DMSO showed the same way as glycerol. Apart from the above, percentage of motility of spermatozoa was observed with respect to different thawing temperatures. Maximum motility was observed at the thawing temperature of 40oC in catla (85%), Rohu (80.00%) and Mrigal (83%). Interesting results were obtained from the fertilization studies of cryopreserved spermatozoa of Catla with the eggs from the matured Catla breeders. Fertilization rate of 75-80% and the hatching rate of 60% was observed from the above study. From the above results, it could be possible to use cryopreserved spermatozoa for commercial production of fish seeds in fish hatcheries.

Keywords


Cryopreservation, Catla, Rohu, Mirgal, DMSO, Fertilization Rate

References





DOI: https://doi.org/10.17485/ijst%2F2013%2Fv6i5%2F33257