Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos
La crioconservación es una herramienta biotecnológica que en peces está orientada principalmente a la conservación criogénica de semen como estrategia de preservación del recurso genético y a su uso para la producción de alevinos con fines diferentes. Actualmente, los protocolos de crioconservación...
- Autores:
-
Medina-Robles, Víctor M.
Duarte-Trujillo, Astrid S.
Cruz-Casallas, Pablo E.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2020
- Institución:
- Universidad de los Llanos
- Repositorio:
- Repositorio Digital Universidad de los LLanos
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unillanos.edu.co:001/3990
- Acceso en línea:
- https://repositorio.unillanos.edu.co/handle/001/3990
https://doi.org/10.22579/20112629.630
- Palabra clave:
- cryobiology
cryopreservation
spermatozoa
fish
semen
criobiología
crioconservación
espermatozoide
peces
semen
criobiologia
criopreservação
esperma
peixe
sêmen
- Rights
- openAccess
- License
- Orinoquia - 2020
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Unillanos2_164a4fb143ff7de0dfe121ee8ef63d36 |
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oai_identifier_str |
oai:repositorio.unillanos.edu.co:001/3990 |
network_acronym_str |
Unillanos2 |
network_name_str |
Repositorio Digital Universidad de los LLanos |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
dc.title.translated.eng.fl_str_mv |
Seminal Cryopreservation in Freshwater Fish: Biotechnological, Cellular and Biochemical Aspects |
title |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
spellingShingle |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos cryobiology cryopreservation spermatozoa fish semen criobiología crioconservación espermatozoide peces semen criobiologia criopreservação esperma peixe sêmen |
title_short |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
title_full |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
title_fullStr |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
title_full_unstemmed |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
title_sort |
Crioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicos |
dc.creator.fl_str_mv |
Medina-Robles, Víctor M. Duarte-Trujillo, Astrid S. Cruz-Casallas, Pablo E. |
dc.contributor.author.spa.fl_str_mv |
Medina-Robles, Víctor M. Duarte-Trujillo, Astrid S. Cruz-Casallas, Pablo E. |
dc.subject.eng.fl_str_mv |
cryobiology cryopreservation spermatozoa fish semen |
topic |
cryobiology cryopreservation spermatozoa fish semen criobiología crioconservación espermatozoide peces semen criobiologia criopreservação esperma peixe sêmen |
dc.subject.spa.fl_str_mv |
criobiología crioconservación espermatozoide peces semen criobiologia criopreservação esperma peixe sêmen |
description |
La crioconservación es una herramienta biotecnológica que en peces está orientada principalmente a la conservación criogénica de semen como estrategia de preservación del recurso genético y a su uso para la producción de alevinos con fines diferentes. Actualmente, los protocolos de crioconservación seminal en peces de agua dulce establecen una amplia variedad de procedimientos cuya efectividad se basa en aspectos ligados a la calidad seminal post-descongelación y la fertilidad, así como su relación con el desarrollo de la progenie. El efecto de la conservación del semen en nitrógeno líquido por periodos amplios de tiempo también toma importancia en ésta biotecnología. Por lo anterior, el objetivo de la presente revisión es describir aspectos biotecnológicos, celulares y bioquímicos asociados al proceso de crioconservación seminal en peces dulceacuícolas, resaltando los avances, las limitaciones y sus perspectivas. |
publishDate |
2020 |
dc.date.accessioned.none.fl_str_mv |
2020-11-20T00:00:00Z 2024-07-25T18:15:04Z |
dc.date.available.none.fl_str_mv |
2020-11-20T00:00:00Z 2024-07-25T18:15:04Z |
dc.date.issued.none.fl_str_mv |
2020-11-20 |
dc.type.spa.fl_str_mv |
Artículo de revista |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.local.eng.fl_str_mv |
Journal article |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.content.spa.fl_str_mv |
Text |
dc.type.coarversion.spa.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
publishedVersion |
dc.identifier.issn.none.fl_str_mv |
0121-3709 |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.unillanos.edu.co/handle/001/3990 |
dc.identifier.doi.none.fl_str_mv |
10.22579/20112629.630 |
dc.identifier.eissn.none.fl_str_mv |
2011-2629 |
dc.identifier.url.none.fl_str_mv |
https://doi.org/10.22579/20112629.630 |
identifier_str_mv |
0121-3709 10.22579/20112629.630 2011-2629 |
url |
https://repositorio.unillanos.edu.co/handle/001/3990 https://doi.org/10.22579/20112629.630 |
dc.language.iso.spa.fl_str_mv |
spa |
language |
spa |
dc.relation.references.spa.fl_str_mv |
Abed-Elmdoust A, Rahimi R, Farahmand H, Amiri BM, Mirvaghefi A, Rafiee G. Droplet vitrification versus straw cryopreservation for spermatozoa banking in Persian sturgeon (Acipenser persicus) from metabolite point of view. Theriogenology, 2019; 129: 110-115. Abinawanto A, Wulandari R, Muchlisin ZA. Effect of egg yolk on the spermatozoa quality of the botia Chromobotia macracanthus (Bleeker, 1852) (Cyprinidae) after short-term cryopreservation. Aquaculture, Aquarium, Conservation & Legislation, 2018; 11 (6): 1737-1744. Alavi SMH, Cosson J. Sperm motility in fishes. (II) Effects of ions and osmolality: A review. Cell Biology International, 2006; 30 (1): 1-14. Alavi SMH, Rodina M, Viveiros ATM, Cosson J, Gela D, Boryshpolets S, Linhart O. Effects of osmolality on sperm morphology, motility and flagellar wave parameters in Northern pike (Esox lucius L.). Theriogenology, 2009; 72 (1): 32-43. Alquézar-Baeta C, Gimeno-Martos S, Miguel-Jiménez S, Santolaria P, Yániz J, Palacín I, Casao A, Cebrián-Pérez JÁ, Muiño-Blanco T, Pérez-Pé R. OpenCASA: A new open-source and scalable tool for sperm quality analysis. PLoS computational biology, 2019; 15 (1): e1006691. Amann RP, Waberski D. Computer-assisted sperm analysis (CASA): capabilities and potential developments. Theriogenology, 2014; 81 (1): 5-17.e3. Atencio-García VJ, Espinosa JA, Martínez JG, Pardo-Carrasco SC. Insemination of bocachico fish (Prochilodus magdalenae) with fresh or cryopreserved semen: effect of spermatozoa/oocyte ratio. Revista Colombiana de Ciencias Pecuarias, 2015; 28 (4): 347-355. Atencio-García V, Longas MD, Petro CM, Pietro-Guevara M, Espinosa-Araujo J. Crioconservación de semen de dorada Brycon moorei con dimetilsulfóxido. Revista Colombiana de Biotecnología, 2017; 19 (2): 81-88. Aulesa C, Cabrera M, Alonso R, Benítez M, Martínez M. Evaluación del sistema automatizado Sperm Class Analyzer® (SCA) para análisis del semen. Revista del Laboratorio Clínico, 2009; 2 (1): 8-16. Benson JD. 2015. Modeling and Optimization of Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 83 – 120. Bernáth G, Bokor Z, Zarski D, Várkonyi L, Hegyi A, Staszny A, Urbányi B, Radóczi J, Horváth A. Commercial-scale out-of-season cryopreservation of Eurasian perch (Perca fluviatilis) sperm and its application for fertilization. Animal Reproduction Science, 2016; 170: 170-177. Blom E. A One-Minute Live-Dead Sperm Stain by Means of Eosin-Nigrosin. Fertility and Sterility, 1950; 1 (2): 176-177. Bobe J, Labbé C. Egg and sperm quality in fish. General and Comparative Endocrinology, 2010; 165 (3): 535-548. Borges AM, Araújo KO, Pivato I, Navarro RD. Ultraestrutura e criopreservação de sêmen de jundiá amazônico (Leiarius marmoratus) em cativeiro. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2020; 72 (1): 253-262. Boryshpolets S, Dzyuba B, Stejskal V, Linhart O. Dynamics of ATP and movement in Eurasian perch (Perca fluviatilis L.) sperm in conditions of decreasing osmolality. Theriogenology, 2009; 72 (6): 851-859. Boryshpolets S, Kholodnyy V, Cosson J, Dzyuba B. Fish sperm motility analysis: the central role of the flagellum. Reproduction, Fertility and Development, 2018; 30 (6): 833-841. Boryshpolets S, Kowalski RK, Dietrich GJ, Dzyuba B, Ciereszko A. Different computer-assisted sperm analysis (CASA) systems highly influence sperm motility parameters. Theriogenology, 2013; 80 (7): 758-765. Butts IAE, Ward MAR, Litvak MK, Pitcher TE, Alavi SMH, Trippel EA, Rideout RM. Automated sperm head morphology analyzer for open-source software. Theriogenology, 2011; 76 (9): 1756-1761.e3. Cabrita E, Gavaia PJ, Riesco MF, Valcarce DG, Sarasquete C, Herráez MP, Robles V. Factors enhancing fish sperm quality and emerging tools for sperm analysis. Aquaculture, 2014; 432: 389-401. Cabrita E, Ma S, Diogo P, Martínez-Páramo S, Sarasquete C, Dinis MT. The influence of certain aminoacids and vitamins on post-thaw fish sperm motility, viability and DNA fragmentation. Animal Reproduction Science, 2011; 125: 189-195. Cabrita E, Sarasquete C, Martínez-Páramo S, Robles V, Beirão J, Pérez-Cerezales S, Herráez MP. Cryopreservation of fish sperm: Applications and perspectives. Journal of Applied Ichthyology, 2010; 26 (5): 623-635. Carneiro PCF, Azevedo HC, Santos JP, Maria AN. Cryopreservation of tambaqui (Colossoma macropomum) semen: Extenders, cryoprotectants, dilution ratios and freezing methods. CryoLetters, 2012; 33 (5): 385-393. Cartón-garcía F, Riesco MF, Cabrita E, Herráez MP, Robles V. Quantification of lesions in nuclear and mitochondrial genes of Sparus aurata cryopreserved sperm. Aquaculture, 2013; 402-403: 106-112. Ciereszko A, Dietrich GJ, Nynca J, Dobosz S, Zalewski T. Cryopreservation of rainbow trout semen using a glucose-methanol extender. Aquaculture, 2014; 420-421: 275-281. Comizzoli P. Advanced biotechnologies for wildlife fertility preservation. Thai Journal of Veterinary Medicine, 2016; 46 (4): 541-545. Cosson J. Frenetic activation of fish spermatozoa flagella entails short‐term motility, portending their precocious decadence. Journal of Fish Biology, 2010; 76 (1): 240-279. Cruz-Casallas PE, Medina-Robles VM, Velasco-Santamaría YM. Protocolo para la crioconservación de semen de yamú (Brycon amazonicus Spix & Agassiz 1829). Revista Colombiana de Ciencias Pecuarias, 2006a; 19 (2): 146-151. Cruz-Casallas PE, Velasco-Santamaría YM, Medina-Robles V. Determinación del espermatocrito y efecto del volumen de la dosis seminante sobre la fertilidad en yamú (Brycon amazonicus). Revista Colombiana de Ciencias Pecuarias, 2006b;19 (2): 140-145. Ding F, Lall SP, Li J, Lei J, Rommens M, Milley JE. Cryobiology cryopreservation of sperm from Atlantic halibut (Hippoglossus hippoglossus, L.) for commercial application. Cryobiology, 2011; 63 (1): 56-60. Draper BW, Moens CB. A High-Throughput method for zebrafish sperm cryopreservation and in vitro fertilization. Journal of Visualized Experiments, 2009; (29): e1395. Dzyuba B, Bondarenko O, Fedorov P, Gazo I, Prokopchuk G, Cosson J. Energetics of fish spermatozoa: The proven and the possible. Aquaculture, 2017; 472: 60-72. Dzyuba BB, Boryshpolets S, Rodina M, Gela D, Linhart O. Spontaneous activation of spermatozoa motility by routine freeze-thawing in different fish species. Journal of Applied Ichthyology, 2010; 26 (5): 720-725. Dzyuba V, Dzyuba B, Cosson J, Boryshpolets S, Yamaner G, Kholodniy V, Rodina M. The antioxidant system of sterlet seminal fluid in testes and Wolffian ducts. Fish Physiology and Biochemistry, 2014; 40 (6): 1731-1739. Dzyuba V, Dzyuba B, Cosson J, Rodina M. Enzyme activity in energy supply of spermatozoon motility in two taxonomically distant fish species (sterlet Acipenser ruthenus, Acipenseriformes and common carp Cyprinus carpio, Cypriniformes). Theriogenology, 2016; 85 (4): 567-574. Engel KM, Grunewald S, Schiller J, Paasch U. Automated semen analysis by SQA Vision ® versus the manual approach — A prospective double‐blind study. Andrologia, 2019; 51 (1): e13149. Evenson DP. 2018. Sperm Chromatin Structure Assay (SCSA®): Evolution from Origin to Clinical Utility. En: Zini A, Agarwal A (Editores). A Clinician’s Guide to Sperm DNA and Chromatin Damage. Springer International Publishing. Montreal, Canada y Cleveland, USA. p. 65 – 90. FAO - Organización de las Naciones Unidas para la Alimentación y la Agricultura. Visión general del sector acuícola nacional: Colombia; [Fecha de acceso: septiembre 2 de 2019] URL: http://www.fao.org/fishery/countrysector/naso_colombia/es#tcN900B1 Faustino F, Silva RCD, Hilbig CC, Makino LC, Senhorini JA, Ninhaus-Silveira A, Nakaghi LSO. Spermatozoon ultrastructure and semen parameters of Brycon vermelha (Characiformes, Characidae). Animal Reproduction Science, 2015; 157: 17-23. Fauvel BC, Suquet M, Cosson J. Evaluation of fish sperm quality. Journal of Applied Ichthyology, 2010; 26 (5): 636-643. Fernandes MDO, Sergio A, Junior V, Acosta IB, Mari S, Gheller M, Corcini CD. Cryopreservation of sperm in annual fish Austrolebias minuano (Cyprinodontiformes; Rivulidae). Aquaculture Research, 2019; 51 (1): 147-154. Fernández A, Gonzalvo M del C, Clavero A, Ruíz de Assín R, Zamora S, Roldán M, Rabelo B, Ramírez JP, Yoldi A, Castilla JA. Fundamentos de criobiología espermática para bancos de semen. Revista ASEBIR, 2009; 14 (1): 17-25. Figueroa E, Lee-estevez M, Valdebenito I, Watanabe I, Oliveira RPS, Romero J. Effects of cryopreservation on mitochondrial function and sperm quality in fish. Aquaculture, 2019; 511: 634190. Figueroa E, Valdebenito I, Farias JG. Technologies used in the study of sperm function in cryopreserved fish spermatozoa. Aquaculture Research, 2016; 47 (6): 1691-1705. Figueroa E, Valdebenito I, Zepeda AB, Figueroa CA, Dumorné K, Castillo RL, Farias JG. Effects of cryopreservation on mitochondria of fish spermatozoa. Reviews in Aquaculture, 2017; 9 (1): 76-87. Fitzpatrick JL, Garcia-gonzalez F, Evans JP. Linking sperm length and velocity: the importance of intramale variation. Biology Letters, 2010; 6 (6): 797-799. Freyhof J, Brooks E (Editores). 2011. European Red List of Freshwater Fishes. Office of the European Union, Luxembourg, p. 70. Gallego V, Pérez L, Asturiano JF, Yoshida M. Relationship between spermatozoa motility parameters, sperm/egg ratio, and fertilization and hatching rates in puffer fish (Takifugu niphobles). Aquaculture, 2013; 416-417: 238-243. Galo JM, Streit-Junior DP, Oliveira CA, Povh JP, Fornari DC, Digmayer M, Ribeiro RP. Quality of fresh and cryopreserved semen and their influence on the rates of fertilization, hatching and quality of the larvae of Piaractus mesopotamicus. Brazilian Journal of Biology, 2019; 79 (3): 438-445. Giaretta E, Munerato M, Yeste M, Galeati G, Spinaci M, Tamanini C, Mari G, Bucci D. Implementing an open-access CASA software for the assessment of stallion sperm motility: Relationship with other sperm quality parameters. Animal Reproduction Science, 2017; 176: 11-19. Gillies EA, Bondarenko V, Cosson J, Pacey AA. Fins improve the swimming performance of fish sperm: a hydrodynamic analysis of the Siberian sturgeon Acipenser baerii. Cytoskeleton, 2013; 70(2): 85-100. Gray J, Hancock GJ. The propulsion of sea-urchin spermatozoa. Journal of Experimental Biology, 1955; 32 (4): 802-814. Grevle I, Ruud K. 2019. Cryopreservation device for biological material. Patente no. US 2019/0166826 A1, Clasificación A01N1 / 0242, p. 4. Gunes S, Sertyel S. 2018. Sperm DNA Damage and Oocyte Repair Capability. En: Zini A, Agarwal A (Editores). A Clinician’s Guide to Sperm DNA and Chromatin Damage. Springer International Publishing. Montreal, Canada y Cleveland, USA. p. 325-350. Guo W, Shao J, Li P, Wu J, Wei Q. Morphology and ultrastructure of Brachymystax lenok tsinlingensis spermatozoa by scanning and transmission electron microscopy. Tissue and Cell, 2016; 48 (4): 321-327. Herrera-Cruz E, Aristizabal-Regino J, Yepes-Blandón J, Estrada-Posada A, Espinosa-Araujo J, Atencio-Garcia V. Criopreservación de semen de bagre rayado Pseudoplatystoma magdaleniatum con tres diferentes crioprotectores. Revista Colombiana de Biotecnología, 2019; 21 (2): 55-62. Horváth Á, Bokor Z, Bernáth G, Csenki Z, Gorjan A, Paz M, Urbányi B. Very low sperm – egg ratios result in successful fertilization using cryopreserved sperm in the Adriatic grayling (Thymallus thymallus). Aquaculture, 2015; 435: 75-77. ICA - Instituto Colombiano Agropecuario. Protección sanitaria de las especies acuícolas [Fecha de acceso: septiembre 2 de 2019] URL: https://www.ica.gov.co/getdoc/b082c759-18c7-47da-bed6-0ebe76b48fe0/acuicolas-(1).aspx İnanan BE, Yılmaz F. Motility evaluation and cryopreservation of fish sperm exposed by water-borne and food-borne boron. Journal of Aquaculture Engineering and Fisheries Research, 2018; 4 (1):12-19. Inkson BJ. 2016. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) for materials characterization. En: Hübschen G, Altpeter I, Tschuncky R, Herrmann HG (Editores). Materials characterization using nondestructive evaluation (NDE) methods. Woodhead Publishing. Duxford, UK, Cambridge, USA y Kidlington, UK. p. 17-43. Irena B, Sarosiek B, Dryl K, Judycka S, Szczepkowska B. The effect of cryopreservation extender on sperm motility and hatch success in northern pike (Esox lucius). Aquaculture, 2020; 514: 734482. Isachenko V, Sánchez R, Rahimi G, Mallmann P, Isachenko E, Merzenich M. Cryoprotectant‐free vitrification of spermatozoa: fish as a model of human. Andrologia, 2018; 51 (1): e13166. Judycka S, Żarski D, Dietrich MA, Palińska-Żarska K, Karol H, Ciereszko A. Standardized cryopreservation protocol of European perch (Perca fluviatilis) semen allows to obtain high fertilization rates with the use of frozen/thawed semen. Aquaculture, 2019; 498: 208-216. Kahwa D, Nyatia E, Rutaisire J, Kaiser H. Spermatozoa morphology and ultrastructure in Nile perch, Lates niloticus (Linnaeus, 1758). African Journal of Aquatic Science, 2019; 44 (1): 97-102. Kashou AH, Sharma R, Agarwal A. 2012. Assessment of Oxidative Stress in Sperm and Semen. En: Carrell DT, Aston KI (Editores). Spermatogenesis. Humana Press. New York, USA. p. 351-361. Kopeika E, Kopeika J, Zhang T. 2007. Cryopreservation of fish sperm. En: Day JG, Stacy G (Editores). Cryopreservation and Freeze-Drying Protocols. Human Press. Totowa, USA. p. 203-217. Kutluyer F, Kayim M, Öğretmen F, Büyükleblebici S, Tuncer PB. Cryopreservation of rainbow trout Oncorhynchus mykiss spermatozoa: Effects of extender supplemented with different antioxidants on sperm motility, velocity and fertility. Cryobiology, 2014; 69(3): 462-466. Lahnsteiner F, Mansour N, Kunz FA. The effect of antioxidants on the quality of cryopreserved semen in two salmonid fish, the brook trout (Salvelinus fontinalis) and the rainbow trout (Oncorhynchus mykiss). Theriogenology, 2011; 76 (5): 882-890. Lahnsteiner F, Mansour N, Plaetzer K. Antioxidant systems of brown trout (Salmo trutta f. fario) semen. Animal Reproduction Science, 2010; 119 (3-4): 314-321. Li P, Guo W, Qiao XM, Liu ZG, Shen L, Wei QW. Morphology and ultrastructure of Dabry’s sturgeon (Acipenser dabryanus) spermatozoa using scanning and transmission electron microscopy. Journal of Applied Ichthyology, 2019; 35 (1): 192-201. - Li P, Hulak M, Koubek P, Sulc M, Dzyuba B, Boryshpolets S, Rodina M, Gela D, Manaskova-Postlerova P, Peknicova J, Linhart O. Ice-age endurance: The effects of cryopreservation on proteins of sperm of common carp, Cyprinus carpio L. Theriogenology, 2010; 74 (3): 413-423. Li P, Hulak M, Li ZH, Sulc M, Psenicka M, Rodina M, Gela D, Linhart O. Cryopreservation of common carp (Cyprinus carpio L.) sperm induces protein phosphorylation in tyrosine and threonine residues. Theriogenology, 2013; 80 (2): 84-89. López-Hernández JC, Osorio-Pérez A, Jiménez-Félix AS, Páramo-Delgadillo S, Márquez-Couturier G, Yasui GS, Arias-Rodríguez L. La calidad espermática en peces y los métodos de evaluación. Revista Ciencias Marinas y Costeras, 2018; 10 (1): 67-96. Maria AN, Azevedo HC, Santos JP, Silva CA, Carneiro PCF. Semen characterization and sperm structure of the Amazon tambaqui Colossoma macropomum. Journal of Applied Ichthyology, 2010; 26 (5): 779-783. Maria AN, Carvalho ACM, Araújo RV, Santos JP, Carneiro PCF, Azevedo HC. Use of cryotubes for the cryopreservation of tambaqui fish semen (Colossoma macropomum). Cryobiology, 2015; 70 (2): 109-114. Martínez JG, Atencio-García V, Pardo-Carrasco S. DNA fragmentation and membrane damage of bocachico Prochilodus magdalenae (Ostariophysi: Prochilodontidae) sperm following cryopreservation with dimethylsulfoxide and glucose. Neotropical Ichthyology, 2012; 10 (3): 577-586. Martínez JG, Pardo S. Effect of freezing and thawing rates on sperm motility in bocachico Prochilodus magdalenae (pisces, characiformes). Revista MVZ Cordoba, 2013; 18 (1): 3295-3303. Martínez-páramo S, Diogo P, Dinis MT, Herráez MP, Sarasquete C. Incorporation of ascorbic acid and α-tocopherol to the extender media to enhance antioxidant system of cryopreserved sea bass sperm. Theriogenology, 2012; 77 (6): 1129-1136. Martínez-Páramo S, Horváth Á, Labbé C, Zhang T, Robles V, Herráez P, Suquet M, Adams S, Viveiros A, Tiersch TR, Cabrita E. Cryobanking of aquatic species. Aquaculture, 2017; 472: 156-177. Mazur P. Kinetics of Water Loss from Cells at Subzero Temperatures and the Likelihood of Intracellular Freezing. The Journal of General Physiology, 1963; 47 (2): 347-369. Mazur P, Leibo SP, Chu EHY. A Two-Factor Hypothesis of Freezing Injury: Evidence from Chinese Hamster Tissue-culture Cells. Experimental Cell Research, 1972; 71 (2): 345-355. Medina-Robles VM, Guaje-Ramírez DN, Marin-Cossio LC, Sandoval-Vargas LY, Cruz-Casallas PE. Crioconservación seminal de Colossoma macropomum como estrategia de producción y conservación en la Orinoquia Colombiana. Revista Orinoquia, 2019; 23 (1): 15-24. Medina-Robles VM, Velasco-Santamaría YM, Cruz-Casallas PE. Los bancos de recursos genéticos y su papel en la conservación de la biodiversidad. Revista Orinoquia, 2006; 10 (1): 71-77. Medina-Robles VM, Velasco-Santamaría YM, Cruz-Casallas PE. Efecto del volumen de empaque sobre la tasa de congelación- descongelación y la fertilidad de semen crioconservado de yamú (Brycon amazonicus). Archivos de Medicina Veterinaria, 2007; 39 (3): 229-237. Melo-Maciel MAP, Nunes JF, Pinheiro JPS, Nunes LT, Pinheiro RRR, Lopes JT, Salmito-Vanderley CSB. Sperm motility and velocities of Characiformes fishes in different times post-activation. Semina: Ciências Agrárias, 2015; 36 (6): 4023-4030. Cunha ATM, Carvalho JDO, Dode MAN. Techniques for sperm evaluation using fluorescent probes. Embrapa Recursos Genéticos e Biotecnologia, 2015; 36 (6): 4365-4376. Miliorini AB, Murgas LDS, Rosa PV, Oberlender G, Pereira GJM, Da Costa DV. A morphological classification proposal for curimba (Prochilodus lineatus) sperm damages after cryopreservation. Aquaculture Research, 2011; 42 (2): 177-187. Miller ME, Kemski M, Grayson JD, Towne K, Dabrowski K. Yellow Perch sperm motility, cryopreservation, and viability of resulting larvae and juveniles. North American Journal of Aquaculture, 2018; 80 (1): 3-12. Mojica JI, Usma JS, Álvarez-León R, Lasso CA (Editores). 2012. Libro rojo de peces dulceacuícolas de Colombia. Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, Instituto de Ciencias Naturales de la Universidad Nacional de Colombia, WWF Colombia y Universidad de Manizales. Bogotá, p. 164. Molnár J, Bokor Z, Várkonyi L, Izsák T, Füzes-Solymosi E, Láng ZL, Csorbai B, Tarnai-Király ZS, Urbányi B, Bernáth G. The systematic development and optimization of large-scale sperm cryopreservation in northern pike (Esox lucius). Cryobiology, 2020; 94: 26-31. Morales AM, Álvarez OG, Ramón M, Pastor FM, Santos MRF, Soler AJ, Garde JJ. Current status and potential of morphometric sperm analysis. Asian Journal of Andrology, 2016; 18 (6): 863-870. Muchlisin ZA, Sarah PI, Aldila DF, Eriani K, Hasri I, Batubara AS, Nur FM, Mustaqim M, Muthmainnah CR, Abinawanto A, Wilkes M. Effect of Dimethyl sulfoxide (DMSO) and egg yolk on sperm motility, fertility and hatching rates of depik Rasbora tawarensis (Pisces: Cyprinidae) eggs after short-term cryopreservation. Aquaculture Research, 2020; 51 (4): 1700-1705. Murgas LDS, Paulino MS, Palhares PC, Miliorini AB, Alves E, Felizardo VDO. Ultrastructural and morphometric analysis of gametes in neotropical teleost fishes. Journal of FisheriesSciences.com, 2017; 11 (1): 56-61. Nynca J, Arnold GJ, Fröhlich T, Ciereszko A. Cryopreservation-induced alterations in protein composition of rainbow trout semen. Proteomics, 2015a; 15 (15): 2643-2654. Nynca J, Dietrich GJ, Dobosz S, Grudniewska J, Ciereszko A. Effect of cryopreservation on sperm motility parameters and fertilizing ability of brown trout semen. Aquaculture, 2014; 433: 62-65. Nynca J, Dietrich GJ, Dobosz S, Zalewski T, Ciereszko A. Effect of postthaw storage time and sperm-to-egg ratio on fertility of cry-opreserved brook trout sperm. Theriogenology, 2015b; 83 (2): 253-256. Nynca J, Dietrich GJ, Grudniewska J, Dobosz S, Liszewska E, Krzy M, Ciereszko A. Efficient method for cryopreservation of European huchen (Hucho hucho L.) and grayling (Thymallus thymallus L.) semen. Aquaculture, 2015c; 435: 146-151. OCDE - Organización para la Cooperación y el Desarrollo Económicos. 2016. Pesca y acuicultura en Colombia. Bogotá, Colombia. Öğretmen F, Inanan BE. Effect of butylated hydroxytoluene (BHT) on the cryopreservation of common carp (Cyprinus carpio) spermatozoa. Animal Reproduction Science, 2014a; 151(3-4): 269-274. Öğretmen F, Inanan BE. Evaluation of the cryoprotective effect of turkish pine honey on common carp (Cyprinus carpio) spermatozoa. CryoLetters, 2014b; 53 (5): 427-437. Öğretmen F, Inanan BE, Kutluyer F, Kayim M. Effect of semen extender supplementation with cysteine on postthaw sperm quality, DNA damage, and fertilizing ability in the common carp (Cyprinus carpio). Theriogenology, 2015; 83 (9): 1548-1552. Öğretmen F, Inanan BE, Öztürk M. Protective effects of propolis on cryopreservation of common carp (Cyprinus carpio) sperm. Cryobiology, 2014; 68 (1): 107-112. Pardo-Carrasco SC, Salas-Villalva J, Reza-Gaviria L, Espinosa-Araujo J, Atencio-García V. Criopreservación de semen de Bagre blanco (Sorubim cuspicaudus) condimetilacetamida como crioprotector. CES Medicina Veterinaria y Zootecnia, 2015; 10 (2): 122-131. Partyka A, Niżański W, Ochota M. 2012. Methods of assessment of cryopreserved semen. En: Katkov II (Editor). Current Frontiers in Cryobiology. InTech. Rijeka, Croatia. p. 547-574. Pegg DE. 2007. Principles of cryopreservation. En: Day JG, Stacy G (Editores). Cryopreservation and Freeze-Drying Protocols. Human Press. Totowa, USA. p. 39-57. Pegg DE. 2015. Principles of Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 3-20. Pérez-Cerezales S, Martínez-Páramo S, Beirão J, Herráez MP. Evaluation of DNA damage as a quality marker for rainbow trout sperm cryopreservation and use of LDL as cryoprotectant. Theriogenology, 2010; 74 (2): 282-289. Pinheiro JPS, Melo-Maciel MAP, Linhares FRA, Lopes JT, Almeida-Monteiro PS, Pinheiro RRR, Torres TM, Salmito-Vanderley C. Use of glucose or BTS TM combined with DMSO or methylglycol under two different freezing protocols for the cryopreservation of sperm from the common curimatã (Prochilodus brevis). Animal Reproduction, 2016; 13 (4): 779-786. Prieto-Mojica CA, Moreno-Nuñez PA, Vicentini CA. Ultraestructura de la espermiogénesis y de los espermatozoides de Gymnocorymbus ternetzi, Hyphessobrycon bifasciatus y de Hyphessobry eques. Revista Colombiana de Ciencias Pecuarias, 2008; 21: 455. Purdy PH, Graham JK. 2015. Membrane Modification Strategies for Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 352-357. Rajasekharan PE. 2017. Conservation of Bioresources. En: Abdulhameed S, Pradeepy NS, Sugathan S (Editores). Bioresources and Bioprocess in Biotechnology. Springer Nature, Singapore. p. 25-47. Ramalho-Santos J, Amaral A, Sousa AP, Rodrigues AS, Martins L, Baptista M, Mota PC, Tavares R, Amaral S, Gamboa S. Probing the Structure and Function of Mammalian Sperm using Optical and Fluorescence Microscopy. Modern Research and Educational Topics in Microscopy, 2007; 1: 394-402. Reis RE, Albert JS, Di Dario F, Mincarone MM, Petry P, Rocha LA. Fish biodiversity and conservation in South America. Journal of Fish Biology, 2016; 89 (1): 12-47. Rodao M, Montagne J, Clivio A, Papa GN, Casanova LG. 2016. Sperm and egg envelope ultrastructure and some considerations on its evolutionary meaning. En: Berois N, García G, De Sá RO (Editores). Annual fishes: Life History Strategy, Diversity and Evolution. CRC Press. Boca Ratón, USA. p. 47-61. Rodríguez-martínez H. Semen evaluation: can we forecast fertility? Veterinarska Stanica, 2019; 50 (4): 293-305. Shaliutina-Kolešová A, Cosson J, Lebeda I, Gazo I, Shaliutina O, Dzyuba B, Linhart O. The influence of cryoprotectants on sturgeon (Acipenser ruthenus) sperm quality, DNA integrity, antioxidant responses, and resistance to oxidative stress. Animal Reproduction Science, 2015; 159: 66-76. Sharma R, Masaki J, Agarwal A. 2013. Sperm DNA fragmentation analysis using the TUNEL assay. En: Carrell D, Aston K (Editores). Spermatogenesis. Humana Press. Totowa, USA. p. 121 – 136. Smith KG, Barrios V, Darwallet WRT, Numa C (Editores). 2014. The status and distribution of freshwater biodiversity in the eastern Mediterranean. International Union for Conservation of Nature (IUCN), Cambridge, Malaga and Gland, p. 149. Takei GL, Mukai C, Okuno M. Transient Ca2+ mobilization caused by osmotic shock initiates salmonid fish sperm motility. Journal of Experimental Biology, 2012; 215 (4): 630-641. Tan E, Yang H, Tiersch TR. Determination of Sperm Concentration for Small-Bodied Biomedical Model Fishes by Use of Microspectrophotometry. Zebrafish, 2010; 7 (2): 233-240. Tedesco PA, Beauchard O, Bigorne R, Blanchet S, Buisson L, Conti L, Cornu JF, Dias MS, Grenouillet G, Hugueny B, Jézéquel C, Leprieur F, Brosse S, Oberdorff T. Data Descriptor: A global database on freshwater fish species occurrence in drainage basins. Scientific Data, 2017; 4: 170141. Tiersch TR. Strategies for commercialization of cryopreserved fish semen. Revista Brasileira de Zootecnia, 2008; 37 (suplemento): 15-19. Ubilla A, Valdebenito I. Use of antioxidants on rainbow trout Oncorhynchus mykiss (Walbaum, 1792) sperm diluent: effects on motility and fertilizing capability. Latin American Journal of Aquatic Research, 2011; 39 (2): 338-343. Varela-Junior AS, Fernandes-Silva E, Figueiredo-Cardoso T, Yokoyama-Namba É, Desessards-Jardim R, Streit-Junior DP, Dahl-Corcini C. The role of dimethyl sulfoxide in the cryopreservation of Curimba (Prochilodus lineatus) semen. Semina: Ciências Agrárias, 2015; 36 (5): 3471-3479. Varela-Junior AS, Goularte KL, Alves JP, Pereira FA, Silva EF, Cardoso TF, Jardim RD, Streit-Junior DP, Corcini CD. Methods of cryopreservation of Tambaqui semen, Colossoma macropomum. Animal Reproduction Science, 2015; 157: 71-77. Várkonyi L, Bokor Z, Molnár J, Fodor F, Szári Z, Ferincz Á, Staszny Á, Láng LZ, Csorbai B, Urbányi B, Bernáth G. The comparison of two different extenders for the improvement of large-scale sperm cryopreservation in common carp (Cyprinus carpio). Reproduction in Domestical Animals, 2019; 54 (3): 639-645. Velasco-Santamaría YM, Medina-Robles VM, Cruz-Casallas PE. Cryopreservation of yamú (Brycon amazonicus) sperm for large scale fertilization. Aquaculture, 2006; 256 (1-4): 264-271. Viveiros ATM, Godinho HP. Sperm quality and cryopreservation of Brazilian freshwater fish species: A review. Fish Physiology and Biochemistry, 2009; 35 (1): 137-150. Viveiros AT, Maria AN, Amaral TB, Orfão LH, Isau ZA, Veríssimo‐Silveira R. Spermatozoon ultrastructure and sperm cryopreservation of the Brazilian dry season spawner fish pirapitinga, Brycon nattereri. Aquaculture Research, 2012; 43 (4): 546-555. Viveiros ATM, Nascimento AF, Orfão LH, Isaú ZA. Motility and fertility of the subtropical freshwater fish streaked prochilod (Prochilodus lineatus) sperm cryopreserved in powdered coconut water. Theriogenology, 2010; 74 (4): 551-556. Viveiros ATM, Oliveira A V, Maria AN, Orfão LH, Souza JC. Sensibilidade dos espermatozoides de dourado (Salminus brasiliensis) a diferentes soluções crioprotetoras. Arquivo Brasileiro de Medicina Veterinaria e Zootecnia, 2009; 61 (4): 883-889. Volpedo A, Thompson GA. Environmental changes on freshwater fish communities in South America in the last five decades: a case study in northeast Argentina. Sustainability, Agri, Food and Environmental Research, 2017; 4 (3): 47-61. Watson PF, Fuller BJ. 2001. Principles of Cryopreservation Gametes and Embryos. En: Watson PF, Holt WV (Editores). Cryobanking the Genetic Resource: Wildlife Conservation for the Future? Taylor & Francis. London, UK. p. 21-46. Weingartner M, Zanandrea ACV, Zaniboni-Filho E. Cryopreserved sperm for oocyte fertilization of dourado Salminus brasiliensis. Ciência Rural, 2015; 45 (5): 892-897. Wilson-leedy JG, Ingermann RL. Development of a novel CASA system based on open source software for characterization of zebrafish sperm motility parameters. Theriogenology, 2007; 67: 661-672. Woelders H, Chaveiro A. Theoretical prediction of “optimal” freezing programmes. Cryobiology, 2004; 49 (3): 258-271. WWF – World Wildlife Fund. 2018. Living planet report - 2018: Aiming Higher. Gland, Switzerland. Yang H, Tiersch TR. Comparative Biochemistry and Physiology, Part C Current status of sperm cryopreservation in biomedical research fish models: Zebra fish, medaka, and Xiphophorus. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 2009; 149 (2): 224-232. Yang S, Zhang X, Liu X, Hu J, Wang Y, Du Z, Yan T. Chorion surface ultrastructure of loach Misgurnus anguillicaudatus: adaptation to the environment and correlation with the reproductive strategy. Journal of Natural History, 2014; 48(35-36): 2207-2218. Yasui GS, Fujimoto T, Arias-rodriguez L, Takagi Y, Arai K. The effect of ions and cryoprotectants upon sperm motility and fertilization success in the loach Misgurnus anguillicaudatus. Aquaculture, 2012; 344-349: 147-152. Yildiz C, Yavas I, Bozkurt Y, Aksoy M. Cryobiology Effect of cholesterol-loaded cyclodextrin on cryosurvival and fertility of cryopreserved carp (Cyprinus carpio) sperm. Criobiology, 2015; 70 (2): 190-194. |
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Medina-Robles, Víctor M.Duarte-Trujillo, Astrid S.Cruz-Casallas, Pablo E.2020-11-20T00:00:00Z2024-07-25T18:15:04Z2020-11-20T00:00:00Z2024-07-25T18:15:04Z2020-11-200121-3709https://repositorio.unillanos.edu.co/handle/001/399010.22579/20112629.6302011-2629https://doi.org/10.22579/20112629.630La crioconservación es una herramienta biotecnológica que en peces está orientada principalmente a la conservación criogénica de semen como estrategia de preservación del recurso genético y a su uso para la producción de alevinos con fines diferentes. Actualmente, los protocolos de crioconservación seminal en peces de agua dulce establecen una amplia variedad de procedimientos cuya efectividad se basa en aspectos ligados a la calidad seminal post-descongelación y la fertilidad, así como su relación con el desarrollo de la progenie. El efecto de la conservación del semen en nitrógeno líquido por periodos amplios de tiempo también toma importancia en ésta biotecnología. Por lo anterior, el objetivo de la presente revisión es describir aspectos biotecnológicos, celulares y bioquímicos asociados al proceso de crioconservación seminal en peces dulceacuícolas, resaltando los avances, las limitaciones y sus perspectivas.Cryopreservation is a biotechnological tool that in fish is mainly aimed at cryogenic conservation of semen as a strategy for preserving the genetic resource and its use for the production of fingerlings with different purposes. Currently, seminal cryopreservation protocols in freshwater fish establish a wide variety of procedures whose effectiveness is based on aspects linked to seminal post-thaw quality and fertility, as well as its relationship with the development of the progeny. The effect of preserving semen in liquid nitrogen for extended periods of time also plays an important role in this biotechnology. Therefore, the objective of this review is to describe biotechnological, cellular and biochemical aspects associated with the seminal cryopreservation process in freshwater fish, highlighting the advances, limitations and perspectives.application/pdfspaUniversidad de los LlanosOrinoquia - 2020https://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/view/630cryobiologycryopreservationspermatozoafishsemencriobiologíacrioconservaciónespermatozoidepecessemencriobiologiacriopreservaçãoespermapeixesêmenCrioconservación seminal en peces de agua dulce: aspectos biotecnológicos, celulares y bioquímicosSeminal Cryopreservation in Freshwater Fish: Biotechnological, Cellular and Biochemical AspectsArtículo de revistainfo:eu-repo/semantics/articleJournal articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Texthttp://purl.org/coar/version/c_970fb48d4fbd8a85Abed-Elmdoust A, Rahimi R, Farahmand H, Amiri BM, Mirvaghefi A, Rafiee G. Droplet vitrification versus straw cryopreservation for spermatozoa banking in Persian sturgeon (Acipenser persicus) from metabolite point of view. Theriogenology, 2019; 129: 110-115.Abinawanto A, Wulandari R, Muchlisin ZA. Effect of egg yolk on the spermatozoa quality of the botia Chromobotia macracanthus (Bleeker, 1852) (Cyprinidae) after short-term cryopreservation. Aquaculture, Aquarium, Conservation & Legislation, 2018; 11 (6): 1737-1744.Alavi SMH, Cosson J. Sperm motility in fishes. (II) Effects of ions and osmolality: A review. Cell Biology International, 2006; 30 (1): 1-14.Alavi SMH, Rodina M, Viveiros ATM, Cosson J, Gela D, Boryshpolets S, Linhart O. Effects of osmolality on sperm morphology, motility and flagellar wave parameters in Northern pike (Esox lucius L.). Theriogenology, 2009; 72 (1): 32-43.Alquézar-Baeta C, Gimeno-Martos S, Miguel-Jiménez S, Santolaria P, Yániz J, Palacín I, Casao A, Cebrián-Pérez JÁ, Muiño-Blanco T, Pérez-Pé R. OpenCASA: A new open-source and scalable tool for sperm quality analysis. PLoS computational biology, 2019; 15 (1): e1006691.Amann RP, Waberski D. Computer-assisted sperm analysis (CASA): capabilities and potential developments. Theriogenology, 2014; 81 (1): 5-17.e3.Atencio-García VJ, Espinosa JA, Martínez JG, Pardo-Carrasco SC. Insemination of bocachico fish (Prochilodus magdalenae) with fresh or cryopreserved semen: effect of spermatozoa/oocyte ratio. Revista Colombiana de Ciencias Pecuarias, 2015; 28 (4): 347-355.Atencio-García V, Longas MD, Petro CM, Pietro-Guevara M, Espinosa-Araujo J. Crioconservación de semen de dorada Brycon moorei con dimetilsulfóxido. Revista Colombiana de Biotecnología, 2017; 19 (2): 81-88.Aulesa C, Cabrera M, Alonso R, Benítez M, Martínez M. Evaluación del sistema automatizado Sperm Class Analyzer® (SCA) para análisis del semen. Revista del Laboratorio Clínico, 2009; 2 (1): 8-16.Benson JD. 2015. Modeling and Optimization of Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 83 – 120.Bernáth G, Bokor Z, Zarski D, Várkonyi L, Hegyi A, Staszny A, Urbányi B, Radóczi J, Horváth A. Commercial-scale out-of-season cryopreservation of Eurasian perch (Perca fluviatilis) sperm and its application for fertilization. Animal Reproduction Science, 2016; 170: 170-177.Blom E. A One-Minute Live-Dead Sperm Stain by Means of Eosin-Nigrosin. Fertility and Sterility, 1950; 1 (2): 176-177.Bobe J, Labbé C. Egg and sperm quality in fish. General and Comparative Endocrinology, 2010; 165 (3): 535-548.Borges AM, Araújo KO, Pivato I, Navarro RD. Ultraestrutura e criopreservação de sêmen de jundiá amazônico (Leiarius marmoratus) em cativeiro. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2020; 72 (1): 253-262.Boryshpolets S, Dzyuba B, Stejskal V, Linhart O. Dynamics of ATP and movement in Eurasian perch (Perca fluviatilis L.) sperm in conditions of decreasing osmolality. Theriogenology, 2009; 72 (6): 851-859.Boryshpolets S, Kholodnyy V, Cosson J, Dzyuba B. Fish sperm motility analysis: the central role of the flagellum. Reproduction, Fertility and Development, 2018; 30 (6): 833-841.Boryshpolets S, Kowalski RK, Dietrich GJ, Dzyuba B, Ciereszko A. Different computer-assisted sperm analysis (CASA) systems highly influence sperm motility parameters. Theriogenology, 2013; 80 (7): 758-765.Butts IAE, Ward MAR, Litvak MK, Pitcher TE, Alavi SMH, Trippel EA, Rideout RM. Automated sperm head morphology analyzer for open-source software. Theriogenology, 2011; 76 (9): 1756-1761.e3.Cabrita E, Gavaia PJ, Riesco MF, Valcarce DG, Sarasquete C, Herráez MP, Robles V. Factors enhancing fish sperm quality and emerging tools for sperm analysis. Aquaculture, 2014; 432: 389-401.Cabrita E, Ma S, Diogo P, Martínez-Páramo S, Sarasquete C, Dinis MT. The influence of certain aminoacids and vitamins on post-thaw fish sperm motility, viability and DNA fragmentation. Animal Reproduction Science, 2011; 125: 189-195.Cabrita E, Sarasquete C, Martínez-Páramo S, Robles V, Beirão J, Pérez-Cerezales S, Herráez MP. Cryopreservation of fish sperm: Applications and perspectives. Journal of Applied Ichthyology, 2010; 26 (5): 623-635.Carneiro PCF, Azevedo HC, Santos JP, Maria AN. Cryopreservation of tambaqui (Colossoma macropomum) semen: Extenders, cryoprotectants, dilution ratios and freezing methods. CryoLetters, 2012; 33 (5): 385-393.Cartón-garcía F, Riesco MF, Cabrita E, Herráez MP, Robles V. Quantification of lesions in nuclear and mitochondrial genes of Sparus aurata cryopreserved sperm. Aquaculture, 2013; 402-403: 106-112.Ciereszko A, Dietrich GJ, Nynca J, Dobosz S, Zalewski T. Cryopreservation of rainbow trout semen using a glucose-methanol extender. Aquaculture, 2014; 420-421: 275-281.Comizzoli P. Advanced biotechnologies for wildlife fertility preservation. Thai Journal of Veterinary Medicine, 2016; 46 (4): 541-545.Cosson J. Frenetic activation of fish spermatozoa flagella entails short‐term motility, portending their precocious decadence. Journal of Fish Biology, 2010; 76 (1): 240-279.Cruz-Casallas PE, Medina-Robles VM, Velasco-Santamaría YM. Protocolo para la crioconservación de semen de yamú (Brycon amazonicus Spix & Agassiz 1829). Revista Colombiana de Ciencias Pecuarias, 2006a; 19 (2): 146-151.Cruz-Casallas PE, Velasco-Santamaría YM, Medina-Robles V. Determinación del espermatocrito y efecto del volumen de la dosis seminante sobre la fertilidad en yamú (Brycon amazonicus). Revista Colombiana de Ciencias Pecuarias, 2006b;19 (2): 140-145.Ding F, Lall SP, Li J, Lei J, Rommens M, Milley JE. Cryobiology cryopreservation of sperm from Atlantic halibut (Hippoglossus hippoglossus, L.) for commercial application. Cryobiology, 2011; 63 (1): 56-60.Draper BW, Moens CB. A High-Throughput method for zebrafish sperm cryopreservation and in vitro fertilization. Journal of Visualized Experiments, 2009; (29): e1395.Dzyuba B, Bondarenko O, Fedorov P, Gazo I, Prokopchuk G, Cosson J. Energetics of fish spermatozoa: The proven and the possible. Aquaculture, 2017; 472: 60-72.Dzyuba BB, Boryshpolets S, Rodina M, Gela D, Linhart O. Spontaneous activation of spermatozoa motility by routine freeze-thawing in different fish species. Journal of Applied Ichthyology, 2010; 26 (5): 720-725.Dzyuba V, Dzyuba B, Cosson J, Boryshpolets S, Yamaner G, Kholodniy V, Rodina M. The antioxidant system of sterlet seminal fluid in testes and Wolffian ducts. Fish Physiology and Biochemistry, 2014; 40 (6): 1731-1739.Dzyuba V, Dzyuba B, Cosson J, Rodina M. Enzyme activity in energy supply of spermatozoon motility in two taxonomically distant fish species (sterlet Acipenser ruthenus, Acipenseriformes and common carp Cyprinus carpio, Cypriniformes). Theriogenology, 2016; 85 (4): 567-574.Engel KM, Grunewald S, Schiller J, Paasch U. Automated semen analysis by SQA Vision ® versus the manual approach — A prospective double‐blind study. Andrologia, 2019; 51 (1): e13149.Evenson DP. 2018. Sperm Chromatin Structure Assay (SCSA®): Evolution from Origin to Clinical Utility. En: Zini A, Agarwal A (Editores). A Clinician’s Guide to Sperm DNA and Chromatin Damage. Springer International Publishing. Montreal, Canada y Cleveland, USA. p. 65 – 90.FAO - Organización de las Naciones Unidas para la Alimentación y la Agricultura. Visión general del sector acuícola nacional: Colombia; [Fecha de acceso: septiembre 2 de 2019] URL: http://www.fao.org/fishery/countrysector/naso_colombia/es#tcN900B1Faustino F, Silva RCD, Hilbig CC, Makino LC, Senhorini JA, Ninhaus-Silveira A, Nakaghi LSO. Spermatozoon ultrastructure and semen parameters of Brycon vermelha (Characiformes, Characidae). Animal Reproduction Science, 2015; 157: 17-23.Fauvel BC, Suquet M, Cosson J. Evaluation of fish sperm quality. Journal of Applied Ichthyology, 2010; 26 (5): 636-643.Fernandes MDO, Sergio A, Junior V, Acosta IB, Mari S, Gheller M, Corcini CD. Cryopreservation of sperm in annual fish Austrolebias minuano (Cyprinodontiformes; Rivulidae). Aquaculture Research, 2019; 51 (1): 147-154.Fernández A, Gonzalvo M del C, Clavero A, Ruíz de Assín R, Zamora S, Roldán M, Rabelo B, Ramírez JP, Yoldi A, Castilla JA. Fundamentos de criobiología espermática para bancos de semen. Revista ASEBIR, 2009; 14 (1): 17-25.Figueroa E, Lee-estevez M, Valdebenito I, Watanabe I, Oliveira RPS, Romero J. Effects of cryopreservation on mitochondrial function and sperm quality in fish. Aquaculture, 2019; 511: 634190.Figueroa E, Valdebenito I, Farias JG. Technologies used in the study of sperm function in cryopreserved fish spermatozoa. Aquaculture Research, 2016; 47 (6): 1691-1705.Figueroa E, Valdebenito I, Zepeda AB, Figueroa CA, Dumorné K, Castillo RL, Farias JG. Effects of cryopreservation on mitochondria of fish spermatozoa. Reviews in Aquaculture, 2017; 9 (1): 76-87.Fitzpatrick JL, Garcia-gonzalez F, Evans JP. Linking sperm length and velocity: the importance of intramale variation. Biology Letters, 2010; 6 (6): 797-799.Freyhof J, Brooks E (Editores). 2011. European Red List of Freshwater Fishes. Office of the European Union, Luxembourg, p. 70.Gallego V, Pérez L, Asturiano JF, Yoshida M. Relationship between spermatozoa motility parameters, sperm/egg ratio, and fertilization and hatching rates in puffer fish (Takifugu niphobles). Aquaculture, 2013; 416-417: 238-243.Galo JM, Streit-Junior DP, Oliveira CA, Povh JP, Fornari DC, Digmayer M, Ribeiro RP. Quality of fresh and cryopreserved semen and their influence on the rates of fertilization, hatching and quality of the larvae of Piaractus mesopotamicus. Brazilian Journal of Biology, 2019; 79 (3): 438-445.Giaretta E, Munerato M, Yeste M, Galeati G, Spinaci M, Tamanini C, Mari G, Bucci D. Implementing an open-access CASA software for the assessment of stallion sperm motility: Relationship with other sperm quality parameters. Animal Reproduction Science, 2017; 176: 11-19.Gillies EA, Bondarenko V, Cosson J, Pacey AA. Fins improve the swimming performance of fish sperm: a hydrodynamic analysis of the Siberian sturgeon Acipenser baerii. Cytoskeleton, 2013; 70(2): 85-100.Gray J, Hancock GJ. The propulsion of sea-urchin spermatozoa. Journal of Experimental Biology, 1955; 32 (4): 802-814.Grevle I, Ruud K. 2019. Cryopreservation device for biological material. Patente no. US 2019/0166826 A1, Clasificación A01N1 / 0242, p. 4.Gunes S, Sertyel S. 2018. Sperm DNA Damage and Oocyte Repair Capability. En: Zini A, Agarwal A (Editores). A Clinician’s Guide to Sperm DNA and Chromatin Damage. Springer International Publishing. Montreal, Canada y Cleveland, USA. p. 325-350.Guo W, Shao J, Li P, Wu J, Wei Q. Morphology and ultrastructure of Brachymystax lenok tsinlingensis spermatozoa by scanning and transmission electron microscopy. Tissue and Cell, 2016; 48 (4): 321-327.Herrera-Cruz E, Aristizabal-Regino J, Yepes-Blandón J, Estrada-Posada A, Espinosa-Araujo J, Atencio-Garcia V. Criopreservación de semen de bagre rayado Pseudoplatystoma magdaleniatum con tres diferentes crioprotectores. Revista Colombiana de Biotecnología, 2019; 21 (2): 55-62.Horváth Á, Bokor Z, Bernáth G, Csenki Z, Gorjan A, Paz M, Urbányi B. Very low sperm – egg ratios result in successful fertilization using cryopreserved sperm in the Adriatic grayling (Thymallus thymallus). Aquaculture, 2015; 435: 75-77.ICA - Instituto Colombiano Agropecuario. Protección sanitaria de las especies acuícolas [Fecha de acceso: septiembre 2 de 2019] URL: https://www.ica.gov.co/getdoc/b082c759-18c7-47da-bed6-0ebe76b48fe0/acuicolas-(1).aspxİnanan BE, Yılmaz F. Motility evaluation and cryopreservation of fish sperm exposed by water-borne and food-borne boron. Journal of Aquaculture Engineering and Fisheries Research, 2018; 4 (1):12-19.Inkson BJ. 2016. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) for materials characterization. En: Hübschen G, Altpeter I, Tschuncky R, Herrmann HG (Editores). Materials characterization using nondestructive evaluation (NDE) methods. Woodhead Publishing. Duxford, UK, Cambridge, USA y Kidlington, UK. p. 17-43.Irena B, Sarosiek B, Dryl K, Judycka S, Szczepkowska B. The effect of cryopreservation extender on sperm motility and hatch success in northern pike (Esox lucius). Aquaculture, 2020; 514: 734482.Isachenko V, Sánchez R, Rahimi G, Mallmann P, Isachenko E, Merzenich M. Cryoprotectant‐free vitrification of spermatozoa: fish as a model of human. Andrologia, 2018; 51 (1): e13166.Judycka S, Żarski D, Dietrich MA, Palińska-Żarska K, Karol H, Ciereszko A. Standardized cryopreservation protocol of European perch (Perca fluviatilis) semen allows to obtain high fertilization rates with the use of frozen/thawed semen. Aquaculture, 2019; 498: 208-216.Kahwa D, Nyatia E, Rutaisire J, Kaiser H. Spermatozoa morphology and ultrastructure in Nile perch, Lates niloticus (Linnaeus, 1758). African Journal of Aquatic Science, 2019; 44 (1): 97-102.Kashou AH, Sharma R, Agarwal A. 2012. Assessment of Oxidative Stress in Sperm and Semen. En: Carrell DT, Aston KI (Editores). Spermatogenesis. Humana Press. New York, USA. p. 351-361.Kopeika E, Kopeika J, Zhang T. 2007. Cryopreservation of fish sperm. En: Day JG, Stacy G (Editores). Cryopreservation and Freeze-Drying Protocols. Human Press. Totowa, USA. p. 203-217.Kutluyer F, Kayim M, Öğretmen F, Büyükleblebici S, Tuncer PB. Cryopreservation of rainbow trout Oncorhynchus mykiss spermatozoa: Effects of extender supplemented with different antioxidants on sperm motility, velocity and fertility. Cryobiology, 2014; 69(3): 462-466.Lahnsteiner F, Mansour N, Kunz FA. The effect of antioxidants on the quality of cryopreserved semen in two salmonid fish, the brook trout (Salvelinus fontinalis) and the rainbow trout (Oncorhynchus mykiss). Theriogenology, 2011; 76 (5): 882-890.Lahnsteiner F, Mansour N, Plaetzer K. Antioxidant systems of brown trout (Salmo trutta f. fario) semen. Animal Reproduction Science, 2010; 119 (3-4): 314-321.Li P, Guo W, Qiao XM, Liu ZG, Shen L, Wei QW. Morphology and ultrastructure of Dabry’s sturgeon (Acipenser dabryanus) spermatozoa using scanning and transmission electron microscopy. Journal of Applied Ichthyology, 2019; 35 (1): 192-201. - Li P, Hulak M, Koubek P, Sulc M, Dzyuba B, Boryshpolets S, Rodina M, Gela D, Manaskova-Postlerova P, Peknicova J, Linhart O. Ice-age endurance: The effects of cryopreservation on proteins of sperm of common carp, Cyprinus carpio L. Theriogenology, 2010; 74 (3): 413-423.Li P, Hulak M, Li ZH, Sulc M, Psenicka M, Rodina M, Gela D, Linhart O. Cryopreservation of common carp (Cyprinus carpio L.) sperm induces protein phosphorylation in tyrosine and threonine residues. Theriogenology, 2013; 80 (2): 84-89.López-Hernández JC, Osorio-Pérez A, Jiménez-Félix AS, Páramo-Delgadillo S, Márquez-Couturier G, Yasui GS, Arias-Rodríguez L. La calidad espermática en peces y los métodos de evaluación. Revista Ciencias Marinas y Costeras, 2018; 10 (1): 67-96.Maria AN, Azevedo HC, Santos JP, Silva CA, Carneiro PCF. Semen characterization and sperm structure of the Amazon tambaqui Colossoma macropomum. Journal of Applied Ichthyology, 2010; 26 (5): 779-783.Maria AN, Carvalho ACM, Araújo RV, Santos JP, Carneiro PCF, Azevedo HC. Use of cryotubes for the cryopreservation of tambaqui fish semen (Colossoma macropomum). Cryobiology, 2015; 70 (2): 109-114.Martínez JG, Atencio-García V, Pardo-Carrasco S. DNA fragmentation and membrane damage of bocachico Prochilodus magdalenae (Ostariophysi: Prochilodontidae) sperm following cryopreservation with dimethylsulfoxide and glucose. Neotropical Ichthyology, 2012; 10 (3): 577-586.Martínez JG, Pardo S. Effect of freezing and thawing rates on sperm motility in bocachico Prochilodus magdalenae (pisces, characiformes). Revista MVZ Cordoba, 2013; 18 (1): 3295-3303.Martínez-páramo S, Diogo P, Dinis MT, Herráez MP, Sarasquete C. Incorporation of ascorbic acid and α-tocopherol to the extender media to enhance antioxidant system of cryopreserved sea bass sperm. Theriogenology, 2012; 77 (6): 1129-1136.Martínez-Páramo S, Horváth Á, Labbé C, Zhang T, Robles V, Herráez P, Suquet M, Adams S, Viveiros A, Tiersch TR, Cabrita E. Cryobanking of aquatic species. Aquaculture, 2017; 472: 156-177.Mazur P. Kinetics of Water Loss from Cells at Subzero Temperatures and the Likelihood of Intracellular Freezing. The Journal of General Physiology, 1963; 47 (2): 347-369.Mazur P, Leibo SP, Chu EHY. A Two-Factor Hypothesis of Freezing Injury: Evidence from Chinese Hamster Tissue-culture Cells. Experimental Cell Research, 1972; 71 (2): 345-355.Medina-Robles VM, Guaje-Ramírez DN, Marin-Cossio LC, Sandoval-Vargas LY, Cruz-Casallas PE. Crioconservación seminal de Colossoma macropomum como estrategia de producción y conservación en la Orinoquia Colombiana. Revista Orinoquia, 2019; 23 (1): 15-24.Medina-Robles VM, Velasco-Santamaría YM, Cruz-Casallas PE. Los bancos de recursos genéticos y su papel en la conservación de la biodiversidad. Revista Orinoquia, 2006; 10 (1): 71-77.Medina-Robles VM, Velasco-Santamaría YM, Cruz-Casallas PE. Efecto del volumen de empaque sobre la tasa de congelación- descongelación y la fertilidad de semen crioconservado de yamú (Brycon amazonicus). Archivos de Medicina Veterinaria, 2007; 39 (3): 229-237.Melo-Maciel MAP, Nunes JF, Pinheiro JPS, Nunes LT, Pinheiro RRR, Lopes JT, Salmito-Vanderley CSB. Sperm motility and velocities of Characiformes fishes in different times post-activation. Semina: Ciências Agrárias, 2015; 36 (6): 4023-4030.Cunha ATM, Carvalho JDO, Dode MAN. Techniques for sperm evaluation using fluorescent probes. Embrapa Recursos Genéticos e Biotecnologia, 2015; 36 (6): 4365-4376.Miliorini AB, Murgas LDS, Rosa PV, Oberlender G, Pereira GJM, Da Costa DV. A morphological classification proposal for curimba (Prochilodus lineatus) sperm damages after cryopreservation. Aquaculture Research, 2011; 42 (2): 177-187.Miller ME, Kemski M, Grayson JD, Towne K, Dabrowski K. Yellow Perch sperm motility, cryopreservation, and viability of resulting larvae and juveniles. North American Journal of Aquaculture, 2018; 80 (1): 3-12.Mojica JI, Usma JS, Álvarez-León R, Lasso CA (Editores). 2012. Libro rojo de peces dulceacuícolas de Colombia. Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, Instituto de Ciencias Naturales de la Universidad Nacional de Colombia, WWF Colombia y Universidad de Manizales. Bogotá, p. 164. Molnár J, Bokor Z, Várkonyi L, Izsák T, Füzes-Solymosi E, Láng ZL, Csorbai B, Tarnai-Király ZS, Urbányi B, Bernáth G. The systematic development and optimization of large-scale sperm cryopreservation in northern pike (Esox lucius). Cryobiology, 2020; 94: 26-31.Morales AM, Álvarez OG, Ramón M, Pastor FM, Santos MRF, Soler AJ, Garde JJ. Current status and potential of morphometric sperm analysis. Asian Journal of Andrology, 2016; 18 (6): 863-870.Muchlisin ZA, Sarah PI, Aldila DF, Eriani K, Hasri I, Batubara AS, Nur FM, Mustaqim M, Muthmainnah CR, Abinawanto A, Wilkes M. Effect of Dimethyl sulfoxide (DMSO) and egg yolk on sperm motility, fertility and hatching rates of depik Rasbora tawarensis (Pisces: Cyprinidae) eggs after short-term cryopreservation. Aquaculture Research, 2020; 51 (4): 1700-1705.Murgas LDS, Paulino MS, Palhares PC, Miliorini AB, Alves E, Felizardo VDO. Ultrastructural and morphometric analysis of gametes in neotropical teleost fishes. Journal of FisheriesSciences.com, 2017; 11 (1): 56-61.Nynca J, Arnold GJ, Fröhlich T, Ciereszko A. Cryopreservation-induced alterations in protein composition of rainbow trout semen. Proteomics, 2015a; 15 (15): 2643-2654.Nynca J, Dietrich GJ, Dobosz S, Grudniewska J, Ciereszko A. Effect of cryopreservation on sperm motility parameters and fertilizing ability of brown trout semen. Aquaculture, 2014; 433: 62-65.Nynca J, Dietrich GJ, Dobosz S, Zalewski T, Ciereszko A. Effect of postthaw storage time and sperm-to-egg ratio on fertility of cry-opreserved brook trout sperm. Theriogenology, 2015b; 83 (2): 253-256.Nynca J, Dietrich GJ, Grudniewska J, Dobosz S, Liszewska E, Krzy M, Ciereszko A. Efficient method for cryopreservation of European huchen (Hucho hucho L.) and grayling (Thymallus thymallus L.) semen. Aquaculture, 2015c; 435: 146-151.OCDE - Organización para la Cooperación y el Desarrollo Económicos. 2016. Pesca y acuicultura en Colombia. Bogotá, Colombia.Öğretmen F, Inanan BE. Effect of butylated hydroxytoluene (BHT) on the cryopreservation of common carp (Cyprinus carpio) spermatozoa. Animal Reproduction Science, 2014a; 151(3-4): 269-274.Öğretmen F, Inanan BE. Evaluation of the cryoprotective effect of turkish pine honey on common carp (Cyprinus carpio) spermatozoa. CryoLetters, 2014b; 53 (5): 427-437.Öğretmen F, Inanan BE, Kutluyer F, Kayim M. Effect of semen extender supplementation with cysteine on postthaw sperm quality, DNA damage, and fertilizing ability in the common carp (Cyprinus carpio). Theriogenology, 2015; 83 (9): 1548-1552.Öğretmen F, Inanan BE, Öztürk M. Protective effects of propolis on cryopreservation of common carp (Cyprinus carpio) sperm. Cryobiology, 2014; 68 (1): 107-112. Pardo-Carrasco SC, Salas-Villalva J, Reza-Gaviria L, Espinosa-Araujo J, Atencio-García V. Criopreservación de semen de Bagre blanco (Sorubim cuspicaudus) condimetilacetamida como crioprotector. CES Medicina Veterinaria y Zootecnia, 2015; 10 (2): 122-131.Partyka A, Niżański W, Ochota M. 2012. Methods of assessment of cryopreserved semen. En: Katkov II (Editor). Current Frontiers in Cryobiology. InTech. Rijeka, Croatia. p. 547-574.Pegg DE. 2007. Principles of cryopreservation. En: Day JG, Stacy G (Editores). Cryopreservation and Freeze-Drying Protocols. Human Press. Totowa, USA. p. 39-57.Pegg DE. 2015. Principles of Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 3-20.Pérez-Cerezales S, Martínez-Páramo S, Beirão J, Herráez MP. Evaluation of DNA damage as a quality marker for rainbow trout sperm cryopreservation and use of LDL as cryoprotectant. Theriogenology, 2010; 74 (2): 282-289.Pinheiro JPS, Melo-Maciel MAP, Linhares FRA, Lopes JT, Almeida-Monteiro PS, Pinheiro RRR, Torres TM, Salmito-Vanderley C. Use of glucose or BTS TM combined with DMSO or methylglycol under two different freezing protocols for the cryopreservation of sperm from the common curimatã (Prochilodus brevis). Animal Reproduction, 2016; 13 (4): 779-786.Prieto-Mojica CA, Moreno-Nuñez PA, Vicentini CA. Ultraestructura de la espermiogénesis y de los espermatozoides de Gymnocorymbus ternetzi, Hyphessobrycon bifasciatus y de Hyphessobry eques. Revista Colombiana de Ciencias Pecuarias, 2008; 21: 455.Purdy PH, Graham JK. 2015. Membrane Modification Strategies for Cryopreservation. En: Wolkers WF, Oldenhof H (Editores). Cryopreservation and Freeze-Drying Protocols. Humana Press. Hertfordshire, UK. p. 352-357.Rajasekharan PE. 2017. Conservation of Bioresources. En: Abdulhameed S, Pradeepy NS, Sugathan S (Editores). Bioresources and Bioprocess in Biotechnology. Springer Nature, Singapore. p. 25-47.Ramalho-Santos J, Amaral A, Sousa AP, Rodrigues AS, Martins L, Baptista M, Mota PC, Tavares R, Amaral S, Gamboa S. Probing the Structure and Function of Mammalian Sperm using Optical and Fluorescence Microscopy. Modern Research and Educational Topics in Microscopy, 2007; 1: 394-402.Reis RE, Albert JS, Di Dario F, Mincarone MM, Petry P, Rocha LA. Fish biodiversity and conservation in South America. Journal of Fish Biology, 2016; 89 (1): 12-47.Rodao M, Montagne J, Clivio A, Papa GN, Casanova LG. 2016. Sperm and egg envelope ultrastructure and some considerations on its evolutionary meaning. En: Berois N, García G, De Sá RO (Editores). Annual fishes: Life History Strategy, Diversity and Evolution. CRC Press. Boca Ratón, USA. p. 47-61.Rodríguez-martínez H. Semen evaluation: can we forecast fertility? Veterinarska Stanica, 2019; 50 (4): 293-305.Shaliutina-Kolešová A, Cosson J, Lebeda I, Gazo I, Shaliutina O, Dzyuba B, Linhart O. The influence of cryoprotectants on sturgeon (Acipenser ruthenus) sperm quality, DNA integrity, antioxidant responses, and resistance to oxidative stress. Animal Reproduction Science, 2015; 159: 66-76.Sharma R, Masaki J, Agarwal A. 2013. Sperm DNA fragmentation analysis using the TUNEL assay. En: Carrell D, Aston K (Editores). Spermatogenesis. Humana Press. Totowa, USA. p. 121 – 136.Smith KG, Barrios V, Darwallet WRT, Numa C (Editores). 2014. The status and distribution of freshwater biodiversity in the eastern Mediterranean. International Union for Conservation of Nature (IUCN), Cambridge, Malaga and Gland, p. 149.Takei GL, Mukai C, Okuno M. Transient Ca2+ mobilization caused by osmotic shock initiates salmonid fish sperm motility. Journal of Experimental Biology, 2012; 215 (4): 630-641.Tan E, Yang H, Tiersch TR. Determination of Sperm Concentration for Small-Bodied Biomedical Model Fishes by Use of Microspectrophotometry. Zebrafish, 2010; 7 (2): 233-240.Tedesco PA, Beauchard O, Bigorne R, Blanchet S, Buisson L, Conti L, Cornu JF, Dias MS, Grenouillet G, Hugueny B, Jézéquel C, Leprieur F, Brosse S, Oberdorff T. Data Descriptor: A global database on freshwater fish species occurrence in drainage basins. Scientific Data, 2017; 4: 170141.Tiersch TR. Strategies for commercialization of cryopreserved fish semen. Revista Brasileira de Zootecnia, 2008; 37 (suplemento): 15-19.Ubilla A, Valdebenito I. Use of antioxidants on rainbow trout Oncorhynchus mykiss (Walbaum, 1792) sperm diluent: effects on motility and fertilizing capability. Latin American Journal of Aquatic Research, 2011; 39 (2): 338-343.Varela-Junior AS, Fernandes-Silva E, Figueiredo-Cardoso T, Yokoyama-Namba É, Desessards-Jardim R, Streit-Junior DP, Dahl-Corcini C. The role of dimethyl sulfoxide in the cryopreservation of Curimba (Prochilodus lineatus) semen. Semina: Ciências Agrárias, 2015; 36 (5): 3471-3479.Varela-Junior AS, Goularte KL, Alves JP, Pereira FA, Silva EF, Cardoso TF, Jardim RD, Streit-Junior DP, Corcini CD. Methods of cryopreservation of Tambaqui semen, Colossoma macropomum. Animal Reproduction Science, 2015; 157: 71-77.Várkonyi L, Bokor Z, Molnár J, Fodor F, Szári Z, Ferincz Á, Staszny Á, Láng LZ, Csorbai B, Urbányi B, Bernáth G. The comparison of two different extenders for the improvement of large-scale sperm cryopreservation in common carp (Cyprinus carpio). Reproduction in Domestical Animals, 2019; 54 (3): 639-645.Velasco-Santamaría YM, Medina-Robles VM, Cruz-Casallas PE. Cryopreservation of yamú (Brycon amazonicus) sperm for large scale fertilization. Aquaculture, 2006; 256 (1-4): 264-271.Viveiros ATM, Godinho HP. Sperm quality and cryopreservation of Brazilian freshwater fish species: A review. Fish Physiology and Biochemistry, 2009; 35 (1): 137-150.Viveiros AT, Maria AN, Amaral TB, Orfão LH, Isau ZA, Veríssimo‐Silveira R. Spermatozoon ultrastructure and sperm cryopreservation of the Brazilian dry season spawner fish pirapitinga, Brycon nattereri. Aquaculture Research, 2012; 43 (4): 546-555.Viveiros ATM, Nascimento AF, Orfão LH, Isaú ZA. Motility and fertility of the subtropical freshwater fish streaked prochilod (Prochilodus lineatus) sperm cryopreserved in powdered coconut water. Theriogenology, 2010; 74 (4): 551-556.Viveiros ATM, Oliveira A V, Maria AN, Orfão LH, Souza JC. Sensibilidade dos espermatozoides de dourado (Salminus brasiliensis) a diferentes soluções crioprotetoras. Arquivo Brasileiro de Medicina Veterinaria e Zootecnia, 2009; 61 (4): 883-889.Volpedo A, Thompson GA. Environmental changes on freshwater fish communities in South America in the last five decades: a case study in northeast Argentina. Sustainability, Agri, Food and Environmental Research, 2017; 4 (3): 47-61.Watson PF, Fuller BJ. 2001. Principles of Cryopreservation Gametes and Embryos. En: Watson PF, Holt WV (Editores). Cryobanking the Genetic Resource: Wildlife Conservation for the Future? Taylor & Francis. London, UK. p. 21-46.Weingartner M, Zanandrea ACV, Zaniboni-Filho E. Cryopreserved sperm for oocyte fertilization of dourado Salminus brasiliensis. Ciência Rural, 2015; 45 (5): 892-897.Wilson-leedy JG, Ingermann RL. Development of a novel CASA system based on open source software for characterization of zebrafish sperm motility parameters. Theriogenology, 2007; 67: 661-672.Woelders H, Chaveiro A. Theoretical prediction of “optimal” freezing programmes. Cryobiology, 2004; 49 (3): 258-271.WWF – World Wildlife Fund. 2018. Living planet report - 2018: Aiming Higher. Gland, Switzerland.Yang H, Tiersch TR. Comparative Biochemistry and Physiology, Part C Current status of sperm cryopreservation in biomedical research fish models: Zebra fish, medaka, and Xiphophorus. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 2009; 149 (2): 224-232.Yang S, Zhang X, Liu X, Hu J, Wang Y, Du Z, Yan T. Chorion surface ultrastructure of loach Misgurnus anguillicaudatus: adaptation to the environment and correlation with the reproductive strategy. Journal of Natural History, 2014; 48(35-36): 2207-2218.Yasui GS, Fujimoto T, Arias-rodriguez L, Takagi Y, Arai K. The effect of ions and cryoprotectants upon sperm motility and fertilization success in the loach Misgurnus anguillicaudatus. Aquaculture, 2012; 344-349: 147-152.Yildiz C, Yavas I, Bozkurt Y, Aksoy M. Cryobiology Effect of cholesterol-loaded cyclodextrin on cryosurvival and fertility of cryopreserved carp (Cyprinus carpio) sperm. Criobiology, 2015; 70 (2): 190-194.https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/download/630/11687825124OrinoquiaPublicationOREORE.xmltext/xml2678https://repositorio.unillanos.edu.co/bitstreams/7570f697-dff0-4994-bfbb-3ca3f9f60e57/download18b0e1001cf7ce0979f0e70244d84097MD51001/3990oai:repositorio.unillanos.edu.co:001/39902024-07-25 13:15:04.894https://creativecommons.org/licenses/by-nc-sa/4.0/Orinoquia - 2020metadata.onlyhttps://repositorio.unillanos.edu.coRepositorio Universidad de Los Llanosrepositorio@unillanos.edu.co |