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Sperm quality of Colossoma macropomum after room-temperature and cold storage

dc.contributor.authorPires, Luana Barbosa
dc.contributor.authorSanches, Eduardo Antonio [UNESP]
dc.contributor.authorRomagosa, Elizabeth
dc.contributor.authorCorrêa Filho, Ruy Alberto Caetano
dc.contributor.authorNass, Rosiane Araujo Rodrigues
dc.contributor.authorLopera-Barrero, Nelson Mauricio
dc.contributor.authorPovh, Jayme Aparecido
dc.contributor.institutionUniversidade Federal de Mato Grosso do Sul (UFMS)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSAA
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.date.accessioned2019-10-06T15:32:01Z
dc.date.available2019-10-06T15:32:01Z
dc.date.issued2019-06-01
dc.description.abstractThe objective of this study was to evaluate the effects of cold and room-temperature storage on the quality of Colossoma macropomum sperm. The experiment was carried out in December (end of Spring), in Nova Mutum-MT, Brazil, involving nine C. macropomum males (4 years old; 6.4 ± 1.5 kg average weight). The fish were selected and transferred to masonry tanks (4 m3) in a laboratory (water renewal rate: 10 L/s; average water temperature: 28°C). Subsequently, reproduction was induced using 2.5 mg of crude carp pituitary extract/kg and the semen was harvested 240 degree hours after hormonal induction. The following sperm characteristics were analyzed every 5 hr using ImageJ/casa software: total motility (MOT), curvilinear velocity (VCL), average path velocity (VAP), straight-line velocity (VSL), straightness of sperm path (STR), wobble (WOB), progressive motility (PROG), beat cross frequency (BCF) and total number of spermatozoa (NSPZ). A fresh sample of semen from each animal was kept at room temperature (25.3 ± 1.2°C). For analysis of cooled semen, syringes were kept in cooling boxes at an average temperature of 16.9 ± 2.1°C. The reduction (p < 0.05) of MOT in semen kept at room temperature occurred at 10 hr (13.95%); in cooled semen, however, MOT declined at 15 hr (76.87%). At 15 hr, there was practically no MOT in the semen kept at room temperature (0.20%), whereas in the cooled semen this situation was observed only at 35 hr (2.91%) The MOT of cooled sperm was higher (p < 0.05) at all times (except zero time), compared with the semen maintained at room temperature. At 15 hr, the cooled spermatozoa showed higher (p < 0.05) VCL (142.18 μm/s) and BCF (29.72 Hz) than those maintained at room temperature (VCL: 51.18 μm/s; BCF: 19.57 Hz). After 15 hr, only the cooled sperm showed quality. In conclusion, semen cooling allows for extending the viability of C. macropomum spermatozoa from 5 to 10 hr without compromising their quality in most characteristics. At 15 and 25 hr of cooling, sperm viability is still observed, though with decreased quality.en
dc.description.affiliationAnimal Science Graduate Program Faculty of Veterinary Medicine and Animal Science FAMEZ Federal University of Mato Grosso do Sul – UFMS
dc.description.affiliationFishery Engineering Course UNESP
dc.description.affiliationCAUNESP
dc.description.affiliationFishery Institute APTA SAA
dc.description.affiliationDepartment of Animal Science State University of Londrina
dc.description.affiliationUnespFishery Engineering Course UNESP
dc.description.affiliationUnespCAUNESP
dc.format.extent747-753
dc.identifierhttp://dx.doi.org/10.1111/jai.13864
dc.identifier.citationJournal of Applied Ichthyology, v. 35, n. 3, p. 747-753, 2019.
dc.identifier.doi10.1111/jai.13864
dc.identifier.issn1439-0426
dc.identifier.issn0175-8659
dc.identifier.scopus2-s2.0-85060800909
dc.identifier.urihttp://hdl.handle.net/11449/187305
dc.language.isoeng
dc.relation.ispartofJournal of Applied Ichthyology
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.titleSperm quality of Colossoma macropomum after room-temperature and cold storageen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-3971-8410[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Centro de Aquicultura da Unesp, Jaboticabalpt

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