Please use this identifier to cite or link to this item: http://paper.sci.ui.ac.id/jspui/handle/2808.28/57
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dc.contributor.authorAbinawanto-
dc.contributor.authorRahayu, S.-
dc.contributor.authorLestari, Retno-
dc.date.accessioned2016-02-26T09:11:50Z-
dc.date.available2016-02-26T09:11:50Z-
dc.date.issued2013-
dc.identifier.issn1992-6197-
dc.identifier.other10.5829/idosi.gv.2013.10.3.72150en_US
dc.identifier.urihttp://paper.sci.ui.ac.id/jspui/handle/2808.28/57-
dc.description.abstractThe aim of this study was to inversitage the effect of egg yolk as a cryoprotectant on spermatozoa quality of Barbonymus gonionotus, twenty four hours after sub-zero freezing. The ejaculates from a total of three males were diluted with the glucose-base extender + 10% methanol + egg yolk. Egg yolk concentration which was used in this study were: 0%, 5%, 7%, 9%, 11%, 13%, 15% and 17%, respectively. Samples were then equilibrated at 4°C for 10 minutes and were freezed at -34°C for 24 hours. Thawing was carried out at 40°C for 30 seconds. Based on Anova test, there were significant effect (P<0.01) of various concentration of egg yolk on post-thaw sperm motility and viability, but not on post-thaw abnormality, compared to control (0% of egg yolk). According to the Tukey test, the concentration of 15% of egg yolk showed significant difference (P<0.01) on post-thaw motility and viability, respectively. Fifteen percent of egg yolk showed the highest post-thaw sperm motility (96.10±3.31) and sperm viability (85.50±3.11), respectively.en_US
dc.language.isoen_USen_US
dc.publisherInternational Digital Organization for Scientific Informationen_US
dc.relation.ispartofseriesVolume 10;No. 3-
dc.sourceGlobal Veterinaria 10 (3): 318-321, 2013en_US
dc.source.urihttp://idosi.org/gv/gv10(3)13/12.pdfen_US
dc.subjectBarbonymus gonionotusen_US
dc.subjectCryopreservationen_US
dc.subjectEgg Yolken_US
dc.subjectSpermatozoaen_US
dc.titleCryopreservation of Java Barb (Barbonymus gonionotus) Using Egg Yolk as a Cryoprotectanten_US
dc.typeArticleen_US
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