Determinación, diferenciación sexual y pubertad en peces

En piscicultura es de gran utilidad conocer los procesos de determinación sexual y los mecanismos que permiten la diferenciación sexual, así como el momento en el cual se alcanza la madurez y los individuos son capaces de reproducirse. Estos tres procesos son muy flexibles en peces y no solo depende...

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Autores:: Rodríguez-Pulido, José A.
Mira-López, Tatiana María
Cruz- Casallas, Pablo E.

Tipo de recurso:: Article of journal

Fecha de publicación:: 2018

Institución:: Universidad de los Llanos

Repositorio:: Repositorio Digital Universidad de los LLanos

Idioma:: spa

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dc.title.spa.fl_str_mv	Determinación, diferenciación sexual y pubertad en peces
dc.title.translated.eng.fl_str_mv	Sex Determination, Sex Differentiation and Puberty in Fish
title	Determinación, diferenciación sexual y pubertad en peces
spellingShingle	Determinación, diferenciación sexual y pubertad en peces Reproduction sex allocation reproductive maturity evolution physiology Reprodução atribuição sexual maturidade reprodutiva evolução fisiologia Reproducción asignación de sexos madurez reproductiva evolución fisiología
title_short	Determinación, diferenciación sexual y pubertad en peces
title_full	Determinación, diferenciación sexual y pubertad en peces
title_fullStr	Determinación, diferenciación sexual y pubertad en peces
title_full_unstemmed	Determinación, diferenciación sexual y pubertad en peces
title_sort	Determinación, diferenciación sexual y pubertad en peces
dc.creator.fl_str_mv	Rodríguez-Pulido, José A. Mira-López, Tatiana María Cruz- Casallas, Pablo E.
dc.contributor.author.spa.fl_str_mv	Rodríguez-Pulido, José A. Mira-López, Tatiana María Cruz- Casallas, Pablo E.
dc.subject.eng.fl_str_mv	Reproduction sex allocation reproductive maturity evolution physiology Reprodução atribuição sexual maturidade reprodutiva evolução fisiologia
topic	Reproduction sex allocation reproductive maturity evolution physiology Reprodução atribuição sexual maturidade reprodutiva evolução fisiologia Reproducción asignación de sexos madurez reproductiva evolución fisiología
dc.subject.spa.fl_str_mv	Reproducción asignación de sexos madurez reproductiva evolución fisiología
description	En piscicultura es de gran utilidad conocer los procesos de determinación sexual y los mecanismos que permiten la diferenciación sexual, así como el momento en el cual se alcanza la madurez y los individuos son capaces de reproducirse. Estos tres procesos son muy flexibles en peces y no solo dependen de diferentes cascadas de genes, si no que algunos factores ambientales son condicionantes o desencadenantes de ellos. En consecuencia, esta revisión pretende dar una mirada a los últimos avances sobre el tema, particularmente las interpretaciones científicas de los eventos de maduración sexual y sus mecanismos reguladores.
publishDate	2018
dc.date.accessioned.none.fl_str_mv	2018-07-16T00:00:00Z 2024-07-25T18:14:48Z
dc.date.available.none.fl_str_mv	2018-07-16T00:00:00Z 2024-07-25T18:14:48Z
dc.date.issued.none.fl_str_mv	2018-07-16
dc.type.spa.fl_str_mv	Artículo de revista
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dc.identifier.issn.none.fl_str_mv	0121-3709
dc.identifier.uri.none.fl_str_mv	https://repositorio.unillanos.edu.co/handle/001/3928
dc.identifier.doi.none.fl_str_mv	10.22579/20112629.487
dc.identifier.eissn.none.fl_str_mv	2011-2629
dc.identifier.url.none.fl_str_mv	https://doi.org/10.22579/20112629.487
identifier_str_mv	0121-3709 10.22579/20112629.487 2011-2629
url	https://repositorio.unillanos.edu.co/handle/001/3928 https://doi.org/10.22579/20112629.487
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dc.relation.references.spa.fl_str_mv	Alcántar-Vázquez JP. Fisiología de los peces triploides. Lat Am J Aquat Res. 2016;44(1):1-15. Almeida FL, Lopes JS, Crescencio R, Izel ACU, Chagas EC, Boijink C. Early puberty of farmed tambaqui (Colossoma macropomum): Possible influence of male sexual maturation on harvest weight. Aquaculture. 2016;452:224-232. Alves AL, Souza Varela E, Vitti Moro G, Ganeco Kirschnik LN. 2014. Riscos genéticos da produção de híbridos de peixes nativos. Documentos / Embrapa Pesca e Aquicultura, ISSN 2318-1400; 3. Barcellos LJ, Woehl VM, Koakoski G, Oliveira TA, Ferreira D, da Rosa JGS, Fagundes M. Puberty influences stress reactivity in female catfish Rhamdia quelen. Physiol Behav. 2014;128:232-236. Baroiller JF, Guiguen Y, Fostier A. Endocrine and environmental aspects of sex differentiation in fi sh. Cell. Mol. Life Sci. 1999;55:910-931. Baroiller JF, D’Cotta H. Environment and sex determination in farmed fish. Comp. Biochem. Physiol. C. 2001;130:399-409. Baroiller JF, D’Cotta H, Bezault E, Wessels S, Hoerstgen-Schwark G. Tilapia sex determination: where temperature and genetics meet. Comp Biochem Physiol A. 2009;153:30-38 Baroiller JF, D’Cotta H, Shved N, Berishvili G, Toguyeni A, Fostier A, Reinecke M. Oestrogen and insulin-like growth factors during the reproduction and growth of the tilapia Oreochromis niloticus and their interactions. Gen Comp Endocrinol. 2014;205:142-150. Biswas S, Jadhao AG, Pinelli C, Palande NV, Tsutsui K. GnIH and GnRH expressions in the central nervous system and pituitary of Indian major carp, Labeo rohita during ontogeny: an immunocytochemical study. Gen Comp Endocrinol. 2015;220:88-92. Brown EE, Baumann H, Conover DO. Temperature and photoperiod effects on sex determination in a fish. J Exp Mar Bio Ecol. 2014;461:39-43 Budd AM, Banh QQ., Domingos JA & Jerry DR. Approaches, challenges and opportunities for Aquaculture. J Mar Sci Eng. 2015;3:329-355. Bubser M, Fadel JR, Jackson LL, Meador-Woodruff JH, Jing D, Deutch AY. Dopaminergic regulation of orexin neurons. Eur J Neurosci. 2005;21:2993-3001. Cain KE, Pryke SR. Testosterone production in response to exogenous gonadotropin releasing hormone (GnRH challenge) depends on social environment and color polymorphism. Gen Comp Endocrinol. 2017;244:77-85. Carrillo M, Espigares F, Felip A, Escobar S, Molés G, Rodríguez R, Zanuy S. Updating control of puberty in male European sea bass: a holistic approach. Gen Comp Endocrinol. 2015;221:42-53. Chen T, Chen S, Ren C, Hu C, Tang D, Yan A. Two isoforms of leptin in the White-clouds Mountain minnow (Tanichthys albonubes): Differential regulation by estrogen despite similar response to fasting. Gen Comp Endocrinol. 2016;225:174-184. Chi ML, Wen HS, Ni M, He F, Li JF, Qian K, Yin XH. Molecular identification of genes involved in testicular steroid synthesis and characterization of the responses to hormones stimulation in testis of Japanese sea bass (Lateolabrax japonicas). Steroids. 2014;84:92-102. Chun-Wei F, Peter Koopman, JB. Control of mammalian germ cell entry into meiosis. Mol Cell Endocrinol. 2014;382:488-497. Cnaani A, McLean E, Hallerman EM. Effects of growth hormone transgene expression and triploidy on acute stress indicators in Atlantic salmon (Salmo salar L.). Aquaculture. 2013;412:107-116. Coumailleau P, Pellegrini E, Adrio F, Diotel N, Cano-Nicolau J, Nasri A, Kah O. Aromatase, estrogen receptors and brain development in fish and amphibians. Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms, 2015;1849(2):152-162. de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E. 2003. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc. Natl. Acad. Sci. U.S.A. 100, 10972–10976. 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Escobar S, Felip A, Salah M, Zanuy S, Carrillo M. Long-term feeding restriction in prepubertal male sea bass (Dicentrarchus labrax L.) increases the number of apoptotic cells in the testis and affects the onset of puberty and certain reproductive parameters. Aquaculture. 2014;433:504-512. Escobar S, Rocha A, Felip A, Carrillo M, Zanuy S, Kah O, Servili A. Leptin receptor gene in the European sea bass (Dicentrarchus labrax): cloning, phylogeny, tissue distribution and neuroanatomical organization. Gen Comp Endocrinol. 2016;229:100-111. Fairgrieve MR, Shibata Y, Smith EK, Hayman ES, Luckenbach JA. Molecular characterization of the gonadal kisspeptin system: cloning, tissue distribution, gene expression analysis and localization in sablefish (Anoplopoma fimbria). Gen Comp Endocrinol. 2016;225:212-223. Ferrandino I, Monaco A, Grimaldi, MC. 2015. Effects of leptin on FSH cells in the pituitary gland of Podarcis siculus. Comptes rendus biologies, 338(3), 180-184. Franz AC, Faass O, Köllner B, Shved N, Link K, Casanova A, Reinecke M. Endocrine and local IGF-I in the bony fish immune system. Biology. 2016;5(1):9. González A, Fernandino JI, Somoza GM. Effects of 5α-dihydrotestosterone on expression of genes related to steroidogenesis and spermatogenesis during the sex determination and differentiation periods of the pejerrey, Odontesthes bonariensis. Comp Biochem Physiol A Mol Integr Physiol.2015;182:1-7. Gorissen M, Flik G. Leptin in teleostean fish, towards the origins of leptin physiology. J Chem Neuroanat. 2014;(61–62):200-206. Gopurappilly R, Ogawa S, Parhar IS. Functional significance of GnRH and kisspeptin, and their cognate receptors in teleost reproduction. Front Endocrinol. 2013;4:24. Grier HJ, Uribe-Aranzábal MC. 2009. The testis and spermatogenesis teleost. In: Jamieson BMG (Ed.). Reproductive biology and phylogeny of fishes (Agnathans and Neotelestomi). Phylogeny-Reproductive System Viviparity – Spermatozoa. Enfield: Science Publisher. p.119-142. Guzmán JM, Luckenbach JA, da Silva DA, Ylitalo G, Swanson P. Development of approaches to induce puberty in cultured female sablefish (Anoplopoma fimbria). Gen Comp Endocrinol. 2015;221:101-113. Heule C, Göppert C, Salzburger W, Böhne A. Genetics and timing of sex determination in the East African cichlid fish Astatotilapia burtoni. BMC genetics. 2014;15(1):140. Horie Y, Shimizu A, Adachi S, Kobayashi T. Expression and localization of gonadotropic hormone subunits (Gpa, Fshb, and Lhb) in the pituitary during gonadal differentiation in medaka. Gen Comp Endocrinol. 2014;204:173-180. Hussain MA, Song WJ, Wolfe A. There is Kisspeptin – And Then There is Kisspeptin. Trends Endocrinol Metab. 2015;26(10):564-572. Ikegami T, Takeuchi Y, Hur SP, Takemura A. Impacts of moonlight on fish reproduction. Mar Genomics. 2014;14:59-66. Joy KP, Chaube R. Vasotocin–A new player in the control of oocyte maturation and ovulation in fish. Gen Comp Endocrinol. 2015;221:54-63. Kaneko H, Ijiri S, Kobayashi T, Izumi H, Kuramochi Y, Wang DS, Nagahama Y. Gonadal soma-derived factor (gsdf), a TGF-beta superfamily gene, induces testis differentiation in the teleost fish Oreochromis niloticus. Mol Cell Endocrinol. 2015;415:87-99. Labbe C, Robles V, Herraez MP. Epigenetics in fish gametes and early embryo. Aquaculture. 2017;427:93-106. Li CG, Wang H, Chen HJ, Zhao Y, Fu PS, Ji XS. Differential expression analysis of genes involved in high-temperature induced sex differentiation in Nile tilapia. Comp Biochem Physiol B Biochem Mol Biol. 2014;177:36-45. Liu Q, Chen Y, Copeland D, Ball H, Duff RJ, Rockich B, Londraville RL. Expression of leptin receptor gene in developing and adult zebrafish. Gen Comp Endocrinol. 2010;166(2):346-355. Liu XY, Zhang XB, Li MH, Zheng SQ, Liu ZL, Cheng YY, Wang DS. Genome-wide identification, evolution of chromobox family genes and their expression in Nile tilapia. Comp Biochem Physiol B Biochem Mol Biol. 2017;203:25-34. Lomniczi A, Wright H, Ojed SR. Epigenetic regulation of female puberty. Front Neuroendocrinol. 2015;36:90-107. López JM, Sanz-Morello B, González A. Organization of the orexin/hypocretin system in the brain of two basal actinopterygian fishes, the cladistians Polypterus senegalus and Erpetoichthys calabaricus. Peptides. 2014;61:23-37. Luzio A, Santos D, Fontaínhas-Fernandes AA, Monteiro SM, Coimbra AM. Effects of 17α-ethinylestradiol at different water temperatures on zebrafish sex differentiation and gonad development. Aquat Toxicol. 2016;174:22-35. Martins RS, Pinto PI, Guerreiro PM, Zanuy S, Carrillo M, Canário AV. Novel galanin receptors in teleost fish: identification, expression and regulation by sex steroids. General and comparative endocrinology, 2014;205:109-120. Matsuda M, Sakaizumi M. Evolution of the sex-determining gene in the teleostean genus Oryzias. Gen Comp Endocrinol. 2016;239:80-88. Mazón MJ, Molés G, Rocha A, Crespo B, Lan-Chow-Wing O, Espigares F, Gómez A. Gonadotropins in European sea bass: endocrine roles and biotechnological applications. Gen Comp Endocrinol. 2015;221:31-41. Mazzeo I, Peñaranda DS, Gallego V, Baloche S, Nourizadeh-Lillabadi R, Tveiten H, Pérez L. Temperature modulates the progression of vitellogenesis in the European eel. Aquaculture. 2014;434:38-47. Metzger DCH, Shulte PM. Epigenomics in marine fishes. Mar Genomics. 2016;30:43-54. Minkina A, Matson CK, Lindeman RE, Ghyselinck NB, Bardwell VJ, Zarkower D. DMRT1 protects male gonadal cells from retinoid-dependent sexual transdifferentiation. Dev Cell. 2014;29(5):511-520. Muñoz-Cueto JA. 2009. Cerebro y reproducción en peces: bases neurales y neuroendocrinas. En: M. Carrillo (Ed.). Reproducción en acuicultura (pp. 27-96). Observatorio Español de Acuicultura, Consejo Superior de Investigaciones Científicas y Ministerio de Agricultura, Pesca y Alimentación. Nelson JS, Grande T, Wilson MVH. 2016. Fishes of the world. Fifth edition. John Wiley & Sons, Hoboken, 707 pp. Pandit NP, Bhandari RK, Kobayashi Y, Nakamura M. High temperature-induced sterility in the female Nile tilapia, Oreochromis niloticus. Gen Comp Endocrinol. 2015;213:110-117. Park HK, Ahima RS. Physiology of leptin: energy homeostasis, neuroendocrine function and metabolism. Metabolism. 2015;64(1):24-34. Penman DJ, Piferrer F. Fish gonadogenesis. Part 1. Genetic and environmental mechanisms of sex determination. Rev Fish Sci. 2008;16(S1):16-34. Pfennig F, Standke A, Gutzeit HO. The role of Amh signaling in teleost fish – Multiple functions not restricted to the gonads. Gen Comp Endocrinol. 2015;223:87-107. Piferrer F, Guiguen Y. Fish gonadogenesis. Part 2. Molecular biology and genomics of sex differentiation. Rev Fish Sci. 2008;16(S1):35-55. Piferrer F. 2009. Determinación y diferenciación sexual de los peces. En: M. Carrillo (Ed.). Reproducción en acuicultura (pp. 249-336). 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Su B, Peatman E, Shang M, Thresher R, Grewe P, Patil J, Duncan PL. Expression and knockdown of primordial germ cell genes, vasa, nanos and dead end in common carp (Cyprinus carpio) embryos for transgenic sterilization and reduced sexual maturity. Aquaculture. 2014;420:S72-S84. Su B, Shang M, Grewe PM, Patil JG, Peatman E, Perera DA, Liu Z. Suppression and restoration of primordial germ cell marker gene expression in channel catfish, Ictalurus punctatus, using knockdown constructs regulated by copper transport protein gene promoters: Potential for reversible transgenic sterilization. Theriogenology. 2015;84(9):1499-1512. Tokarz J, Möller G, de Angelis MH, Adamski J. Steroids in teleost fishes: a functional point of view. Steroids. 2015;103:123-144. Trippel EA, Butts IA, Babin A, Neil SR, Feindel NJ, Benfey TJ. Effects of reproduction on growth and survival in Atlantic cod, Gadus morhua, assessed by comparison to triploids. J Exp Mar Bio Ecol. 2014;451:35-43. Tzung KW, Goto R, Saju JM, Sreenivasan R, Saito T, Arai K, Orbán, L. Early depletion of primordial germ cells in zebrafish promotes testis formation. Stem Cell Reports. 2015;4(1):61-73. Valentin F.N. 2013. Processo de diferenciação gonadel em Pseudoplatystoma fasciatum e tentativa de feminizacao com 17β-estradiol Vandeputte M, Dupont-Nivet M, Chavanne H, Chatain B. A polygenic hypothesis for sex determination in the European sea bass Dicentrarchus labrax. Genetics. 2007;176:1049-1057. Wang HP, Gao ZX, Rapp D, O’Bryant P, Yao H, Cao XJ. Effects of temperature and genotype on sex determination and sexual size dimorphism of bluegill sunfish Lepomis macrochirus. Aquaculture. 2014;420:S64-S71. Weil C, Le Bail PY, Sabin N, Le Gac F. In vitro action of leptin on FSH and LH production in rainbow trout (Onchorhychus mykiss) at different stages of the sexual cycle. Gen Comp Endocrinol. 2003;130:2-12. Weltzien FA, Hildahl J, Hodne K, Okubo K, Haug TM. Embryonic development of gonadotrope cells and gonadotropic hormones–lessons from model fish. Mol Cell Endocrinol. 2014;385(1-2):18-27. Wong TT, Zohar Y. Production of reproductively sterile fish by a non-transgenic gene silencing technology. Sci Rep. 2015;5:15822. Yildirim Ş, Vardar H. The influence of a longer photoperiod on growth parameters of European sea bass Dicentrarchus labrax (Linnaeus, 1758) reared in sea cages. J Appl Ichthyol. 2015;31(1):100-105. Zhang Z, Lau SW, Zhang L, Ge W. Disruption of zebrafish follicle-stimulating hormone receptor (fshr) but not luteinizing hormone receptor (lhcgr) gene by TALEN leads to failed follicle activation in females followed by sexual reversal to males. Endocrinology, 2015;156(10):3747-3762.
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spelling	Rodríguez-Pulido, José A.Mira-López, Tatiana MaríaCruz- Casallas, Pablo E.2018-07-16T00:00:00Z2024-07-25T18:14:48Z2018-07-16T00:00:00Z2024-07-25T18:14:48Z2018-07-160121-3709https://repositorio.unillanos.edu.co/handle/001/392810.22579/20112629.4872011-2629https://doi.org/10.22579/20112629.487En piscicultura es de gran utilidad conocer los procesos de determinación sexual y los mecanismos que permiten la diferenciación sexual, así como el momento en el cual se alcanza la madurez y los individuos son capaces de reproducirse. Estos tres procesos son muy flexibles en peces y no solo dependen de diferentes cascadas de genes, si no que algunos factores ambientales son condicionantes o desencadenantes de ellos. En consecuencia, esta revisión pretende dar una mirada a los últimos avances sobre el tema, particularmente las interpretaciones científicas de los eventos de maduración sexual y sus mecanismos reguladores.In fish farming is useful to know the processes of sex determination and mechanisms that allow differentiation and the time in which maturation is reached and specimens are able to reproduce, these three processes are very flexible in specimens and not just rely different cascades of genes if some environmental factors are conditions or triggers them. So this review aims to take a look at the latest articles on the subject, scientific interpretations of the events of sexual maturation and their regulatory mechanisms, and review the management of his control.application/pdfspaUniversidad de los LlanosOrinoquia - 2019https://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/487Reproductionsex allocationreproductive maturityevolutionphysiologyReproduçãoatribuição sexualmaturidade reprodutivaevoluçãofisiologiaReproducciónasignación de sexosmadurez reproductivaevoluciónfisiologíaDeterminación, diferenciación sexual y pubertad en pecesSex Determination, Sex Differentiation and Puberty in FishArtículo 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_970fb48d4fbd8a85Alcántar-Vázquez JP. 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Costs of reproduction in a long-lived bird: large clutch size is associated with low survival in the presence of a highly virulent disease. Biol Lett. 2009;5(2):278-281.Diemer O, Bittencourt F, Barcellos LG, Boscolo WR, Feiden A, Romagosa E. Lysine in the diet of Rhamdia voulezi male broodstocks confined in net cages. Aquaculture. 2014;434:93-99.Dutil JD, Lambert Y. Natural mortality from poor condition in Atlantic cod (Gadus morhua). Can J Fish Aquat Sci. 2000;57(4):826-836.Escobar S, Servili A, Espigares F, Gueguen MM, Brocal I, Felip A, Kah O. Expression of kisspeptins and kiss receptors suggests a large range of functions for kisspeptin systems in the brain of the European sea bass. PloS one, 2013;8(7):e70177.Escobar S, Felip A, Salah M, Zanuy S, Carrillo M. Long-term feeding restriction in prepubertal male sea bass (Dicentrarchus labrax L.) increases the number of apoptotic cells in the testis and affects the onset of puberty and certain reproductive parameters. Aquaculture. 2014;433:504-512.Escobar S, Rocha A, Felip A, Carrillo M, Zanuy S, Kah O, Servili A. Leptin receptor gene in the European sea bass (Dicentrarchus labrax): cloning, phylogeny, tissue distribution and neuroanatomical organization. Gen Comp Endocrinol. 2016;229:100-111.Fairgrieve MR, Shibata Y, Smith EK, Hayman ES, Luckenbach JA. Molecular characterization of the gonadal kisspeptin system: cloning, tissue distribution, gene expression analysis and localization in sablefish (Anoplopoma fimbria). Gen Comp Endocrinol. 2016;225:212-223.Ferrandino I, Monaco A, Grimaldi, MC. 2015. Effects of leptin on FSH cells in the pituitary gland of Podarcis siculus. Comptes rendus biologies, 338(3), 180-184.Franz AC, Faass O, Köllner B, Shved N, Link K, Casanova A, Reinecke M. Endocrine and local IGF-I in the bony fish immune system. Biology. 2016;5(1):9.González A, Fernandino JI, Somoza GM. 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Gen Comp Endocrinol. 2015;221:101-113.Heule C, Göppert C, Salzburger W, Böhne A. Genetics and timing of sex determination in the East African cichlid fish Astatotilapia burtoni. BMC genetics. 2014;15(1):140.Horie Y, Shimizu A, Adachi S, Kobayashi T. Expression and localization of gonadotropic hormone subunits (Gpa, Fshb, and Lhb) in the pituitary during gonadal differentiation in medaka. Gen Comp Endocrinol. 2014;204:173-180.Hussain MA, Song WJ, Wolfe A. There is Kisspeptin – And Then There is Kisspeptin. Trends Endocrinol Metab. 2015;26(10):564-572.Ikegami T, Takeuchi Y, Hur SP, Takemura A. Impacts of moonlight on fish reproduction. Mar Genomics. 2014;14:59-66. Joy KP, Chaube R. Vasotocin–A new player in the control of oocyte maturation and ovulation in fish. Gen Comp Endocrinol. 2015;221:54-63.Kaneko H, Ijiri S, Kobayashi T, Izumi H, Kuramochi Y, Wang DS, Nagahama Y. 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Endocrinology, 2015;156(10):3747-3762.https://orinoquia.unillanos.edu.co/index.php/orinoquia/article/download/487/10679118022OrinoquiaPublicationOREORE.xmltext/xml2597https://repositorio.unillanos.edu.co/bitstreams/38e827ba-366f-4d09-8cbb-57042bcd67c6/downloadf4a7eaaa42b05446f319a7a10dbb7c31MD51001/3928oai:repositorio.unillanos.edu.co:001/39282024-07-25 13:14:48.281https://creativecommons.org/licenses/by-nc-sa/4.0/Orinoquia - 2019metadata.onlyhttps://repositorio.unillanos.edu.coRepositorio Universidad de Los Llanosrepositorio@unillanos.edu.co

Determinación, diferenciación sexual y pubertad en peces

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