Mostrar el registro sencillo del documento

Exposición social temprana, aprendizaje y desarrollo de la conducta sexual de la codorniz japonesa (coturnix japonica)

dc.rights.licenseReconocimiento 4.0 Internacional
dc.contributor.advisorGutiérrez Domínguez, Germán Antonio
dc.contributor.authorDuque Escobar, Leonardo Andres
dc.date.accessioned2023-12-12T15:32:59Z
dc.date.available2023-12-12T15:32:59Z
dc.date.issued2023-11-24
dc.identifier.urihttps://repositorio.unal.edu.co/handle/unal/85070
dc.descriptionilustraciones
dc.description.abstractEl presente estudio evaluó cómo la exposición social temprana influye en el desarrollo de la conducta sexual y en el aprendizaje de una tarea de condicionamiento sexual. Noventa y siete codornices macho de 20, 30 y 40 días post eclosión (DPE) fueron asignadas a distintos grupos de exposición (física, visual y sin exposición) con el objetivo de evaluar la influencia de las experiencias tempranas en el desarrollo de la conducta sexual. Los resultados mostraron que un alto grado de exposición a las hembras provocó un retraso en el desarrollo de la conducta sexual en los sujetos más jóvenes (20 DPE). Por el contrario, los sujetos de 30 y 40 días mostraron una mejora en el desempeño de la conducta sexual bajo las mismas condiciones, en comparación con machos que tuvieron una menor exposición. Posteriormente, todos los sujetos pasaron por un procedimiento de aprendizaje en el que se les presentó un estímulo condicionado seguido del acceso copulatorio a las hembras. Los resultados mostraron que independientemente de la edad, los sujetos fueron capaces de ejecutar conductas sexuales frente al estímulo incondicionado. No obstante, únicamente el grupo de 40 días mostró evidencias claras de aprendizaje, ya que ejecutó respuestas de comportamiento sexual frente al estímulo condicionado de manera consistente. Estos hallazgos sugieren que la experiencia temprana con conespecíficos adultos del sexo opuesto influye de manera diferencial en la conducta sexual dependiendo de la edad del sujeto y de la intensidad de dicha exposición. Adicionalmente, los resultados permiten sugerir que para establecer asociaciones en una tarea de tipo sexual es necesario que los sujetos tengan un desarrollo sexual completo. (Texto tomado de la fuente)
dc.description.abstractThe present study assessed how early social exposure influences the development of subsequent sexual behavior and whether this exposure, in turn, has implications for learning in a sexual conditioning task. Ninety-seven male quails of 20, 30, and 40 days post hatching (DPH) were assigned to various exposure groups (physical, visual, and no exposure) with the aim of assessing the influence of early experiences on the development of sexual behavior. The results showed that a high degree of exposure to females led to a delay in the development of sexual behavior in the younger subjects (20 DPH). On the contrary, subjects aged 30 and 40 days exhibited an improvement in sexual behavior performance under the same conditions, compared to males with lower exposure. Subsequently, all subjects underwent a learning procedure in which a conditioned stimulus was presented, followed by copulatory access to females. Regardless of age, subjects showed sexual behaviors in response to the unconditioned stimulus. However, only the 40-day group displayed clear evidence of learning, consistently presenting sexual behavioral responses to the conditioned stimulus. These findings suggest that early experience with adult conspecifics of the opposite sex influences sexual behavior differentially, depending on the subject's age and the intensity of such exposure. Additionally, the results suggest that to establish associations in a sexual-type task, subjects need to have complete sexual development.
dc.format.extentix, 120 páginas
dc.format.mimetypeapplication/pdf
dc.language.isospa
dc.publisherUniversidad Nacional de Colombia
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleExposición social temprana, aprendizaje y desarrollo de la conducta sexual de la codorniz japonesa (coturnix japonica)
dc.typeTrabajo de grado - Maestría
dc.type.driverinfo:eu-repo/semantics/masterThesis
dc.type.versioninfo:eu-repo/semantics/acceptedVersion
dc.publisher.programBogotá - Ciencias Humanas - Maestría en Psicología
dc.contributor.researchgroupAprendizaje y Comportamiento Animal
dc.description.degreelevelMaestría
dc.description.researchareaAprendizaje y Evolución del Comportamiento
dc.identifier.instnameUniversidad Nacional de Colombia
dc.identifier.reponameRepositorio Institucional Universidad Nacional de Colombia
dc.identifier.repourlhttps://repositorio.unal.edu.co/
dc.publisher.facultyFacultad de Ciencias Humanas
dc.publisher.placeBogotá, Colombia
dc.publisher.branchUniversidad Nacional de Colombia - Sede Bogotá
dc.relation.referencesAdkins, E. K. (1975). Hormonal basis of sexual differentiation in the Japanese quail. Journal of Comparative and Physiological Psychology, 89(1), 61–71. https://doi.org/10.1037/h0076406
dc.relation.referencesAdkins, E. K., & Alder, N. T. (1972). Hormonal control of behavior in the Japanese quail. Journal of Comparative and Physiological Psychology, 81(1), 27–36. https://doi.org/10.1037/h0033315
dc.relation.referencesAdkins, E. K., Boop, J. J., Koutnik, D. L., Morris, J. B., & Pniewski, E. E. (1980). Further evidence that androgen aromatization is essential for the activation of copulation in male quail. Physiology & Behavior, 24(3), 441-446. https://doi.org/10.1016/0031-9384(80)90233-4.
dc.relation.referencesAdkins-Regan, E. (1995). Predictors of fertilization in the Japanese quail, Coturnix japonica. Animal Behaviour, 50(5), 1405-1415. https://doi.org/10.1016/0003-3472(95)80055-7.
dc.relation.referencesAdkins, E. K., & Pniewski, E. E. (1978). Control of reproductive behavior by sex steroids in male quail. Journal of Comparative and Physiological Psychology, 92(6), 1169–1178. https://doi.org/10.1037/h0077523
dc.relation.referencesAkins, C. K. (1998). Context excitation and modulation of conditioned sexual behavior. Animal Learning & Behavior, 26(4), 416–426. https://doi.org/10.3758/BF03199234
dc.relation.referencesAkins, C. K., Domjan, M., & Gutierrez, G. (1994). Topography of sexually conditioned behavior in male Japanese quail (Coturnix japonica) depends on the CS–US interval. Journal of Experimental Psychology: Animal Behavior Processes, 20(2), 199-209. https://doi.org/10.1037/0097-7403.20.2.199.
dc.relation.referencesAkter, M. (2019). Physical and psychological vulnerability of adolescents during pregnancy period as well as post traumatic stress and depression after child birth. Open Journal of Social Sciences, 7(01), 170
dc.relation.referencesArbaiza, A. L. (2013). Efectos de la experiencia temprana en el comportamiento sexual de la codorniz japonesa macho (tesis de pregrado). Universidad Nacional de Colombia, Bogotá, Colombia
dc.relation.referencesArbaiza-Bayona, A. L., Arteaga-Avendaño, M. P., Puentes-Escamilla, M., & Gutiérrez, G. (2022). Effects of early social experience on sexual behavior in Japanese quail (Coturnix Japonica). Learning and Behavior, 50(3), 283-97. https://doi.org/10.3758/s13420-022-00527-3
dc.relation.referencesArteaga, M. P. (2015). Experiencia social temprana, receptividad sexual y fertilidad en hembras de codorniz japonesa (tesis de pregrado). Universidad Nacional de Colombia, Bogotá, Colombia.
dc.relation.referencesBall, G. F., & Balthazart, J. (2004). Hormonal regulation of brain circuits mediating male sexual behavior in birds. Physiology & behavior, 83(2), 329-346. https://doi.org/10.1016/j.physbeh.2004.08.020
dc.relation.referencesBall, G. F., & Balthazart, J. (2008). How useful is the appetitive and consummatory distinction for our understanding of the neuroendocrine control of sexual behavior?. Hormones and behavior, 53(2), 307-311. https://doi.org/10.1016/j.yhbeh.2007.09.023
dc.relation.referencesBall, G. F., & Balthazart, J. (2010). Japanese quail as a model system for studying the neuroendocrine control of reproductive and social behaviors. ILAR journal, 51(4), 310-325. https://doi.org/10.1093/ilar.51.4.310
dc.relation.referencesBalthazart, J., Baillien, M., Cornil, C. A., & Ball, G. F. (2004). Preoptic aromatase modulates male sexual behavior: Slow and fast mechanisms of action. Physiology and Behavior, 83(2), 247–270. https://doi.org/10.1016/j.physbeh.2004.08.025
dc.relation.referencesBalthazart, J., Reid, J., Absil, P., Foidart, A., & Ball, G. F. (1995). Appetitive as well as consummatory aspects of male sexual behavior in quail are activated by androgens and estrogens. Behavioral neuroscience, 109(3), 485–501. https://doi.org/10.1037/0735-7044.109.3.485.
dc.relation.referencesBalthazart, J., Schumacher, M., & Ottinger, M. A. (1983). Sexual differences in the Japanese quail: Behavior, morphology, and intracellular metabolism of testosterone. General and Comparative Endocrinology, 51(2), 191–207. https://doi.org/10.1016/0016-6480(83)90072-2
dc.relation.referencesBalthazart, J., Schumacher, M., & Ottinger, M. A. (1983). Sexual differences in the Japanese quail: Behavior, morphology, and intracellular metabolism of testosterone. General and Comparative Endocrinology, 51(2), 191–207. https://doi.org/10.1016/0016-6480(83)90072-2
dc.relation.referencesBeach, F. A., & Jaynes, J. (1954). Effects of early experience upon the behavior of animals. Psychological Bulletin, 51(3), 239–263. https://doi.org/10.1037/h0061176
dc.relation.referencesBell, R. W., & Felbinger, R. J. (1962). Effects of free and restricted environmental experience on the development of socio-sexual behavior in the rat. Psychological Reports, 10(2), 351-356.
dc.relation.referencesBournonville, Dickens, Ball, Balthazart, and C. (2011). Dynamic changes in brain aromatase activity following sexual interactions in males: where, when and why? Bone, 23(1), 1–7. https://doi.org/10.1161/CIRCULATIONAHA.110.956839
dc.relation.referencesBournonville, Dickens, Ball, Balthazart, and C. (2011). Dynamic changes in brain aromatase activity following sexual interactions in males: where, when and why? Bone, 23(1), 1–7. https://doi.org/10.1161/CIRCULATIONAHA.110.956839
dc.relation.referencesCan, A., Domjan, M., & Delville, Y. (2007). Sexual experience modulates neuronal activity in male Japanese quail. Hormones and behavior, 52(5), 590-599. https://doi.org/10.1016/j.yhbeh.2007.07.011
dc.relation.referencesCetinkaya, H., & Domjan, M. (2006). Sexual fetishism in a quail (Coturnix japonica) model system: test of reproductive success. Journal of Comparative Psychology, 120(4), 427-432. https://doi.org/10.1037/0735-7036.120.4.427
dc.relation.referencesCornil, C. A., & Ball, G. F. (2010). Effects of social experience on subsequent sexual performance in naïve male Japanese quail (Coturnix japonica). Hormones and behavior, 57(4-5), 515-522. https://doi.org/10.1016/j.yhbeh.2010.02.010
dc.relation.referencesCornil, C. A., & Ball, G. F. (2010). Effects of social experience on subsequent sexual performance in naïve male Japanese quail (Coturnix japonica). Hormones and behavior, 57(4-5), 515-522. https://doi.org/10.1016/j.yhbeh.2010.02.010
dc.relation.referencesCornil, C. A., & Ball, G. F. (2010). Effects of social experience on subsequent sexual performance in naïve male Japanese quail (Coturnix japonica). Hormones and behavior, 57(4-5), 515-522. https://doi.org/10.1016/j.yhbeh.2010.02.010
dc.relation.referencesCornil, C. A., & Ball, G. F. (2010). Effects of social experience on subsequent sexual performance in naïve male Japanese quail (Coturnix japonica). Hormones and behavior, 57(4-5), 515-522. https://doi.org/10.1016/j.yhbeh.2010.02.010
dc.relation.referencesCornil, C. A., & Ball, G. F. (2010). Effects of social experience on subsequent sexual performance in naïve male Japanese quail (Coturnix japonica). Hormones and behavior, 57(4-5), 515-522. https://doi.org/10.1016/j.yhbeh.2010.02.010
dc.relation.referencesCusato, B., & Domjan, M. (1998). Special efficacy of sexual conditioned stimuli that include species typical cues: Tests with a conditioned stimuli preexposure design. Learning and Motivation, 29(2), 152-167. https://doi.org/10.1006/lmot.1997.0988
dc.relation.referencesDelville, Y., Sulon, J., Hendrick, J. C., & Balthazart, J. (1984). Effect of the presence of females on the pituitary-testicular activity in male Japanese quail (Coturnix coturnix japonica). General and comparative endocrinology, 55(2), 295-305. https://doi.org/10.1016/0016-6480(84)90115-1
dc.relation.referencesDickens, M. J., Cornil, C. A., & Balthazart, J. (2011). Acute stress differentially affects aromatase activity in specific brain nuclei of adult male and female quail. Endocrinology, 152(11), 4242-4251.https://doi.org/10.1210/en.2011-1341Domjan, M., Blesbois, E., & Williams, J. (1998). The adaptive significance of sexual conditioning: Pavlovian control of sperm release. Psychological Science, 9(5), 411-415. https://doi.org/10.1111/1467-9280.00077
dc.relation.referencesDomjan, M., Cusato, B., & Krause, M. (2004). Learning with arbitrary versus ecological conditioned stimuli: Evidence from sexual conditioning. Psychonomic Bulletin & Review, 11, 232-246. https://doi.org/10.3758/BF03196565.
dc.relation.referencesDomjan, M., & Gutiérrez, G. (2019). The behavior system for sexual learning. Behavioural processes, 162, 184-196. https://doi.org/10.1016/j.beproc.2019.01.013
dc.relation.referencesDomjan, M., & Nash, S. (1988). Stimulus control of social behaviour in male Japanese quail, Coturnix coturnix japonica. Animal Behaviour, 36(4), 1006-1015.
dc.relation.referencesGalef, B. G. (2008). Social influences on the mate choices of male and female Japanese quail. Comparative Cognition & Behavior Reviews, 3, 1-12. https://doi.org/10.3819/ccbr.2008.30001
dc.relation.referencesGalef, B. G., & Laland, K. N. (2005). Social learning in animals: empirical studies and theoretical models. Bioscience, 55(6), 489-499. https://doi.org/10.1641/0006-3568(2005)055[0489:SLIAES]2.0.CO;2
dc.relation.referencesGalef, B. G., & Laland, K. N. (2005). Social learning in animals: empirical studies and theoretical models. Bioscience, 55(6), 489-499. https://doi.org/10.1641/0006-3568(2005)055[0489:SLIAES]2.0.CO;2
dc.relation.referencesGallagher, J. E. (1977). Sexual imprinting: A sensitive period in Japanese quail (Coturnix coturnix japonica). Journal of Comparative and Physiological Psychology, 91(1), 72–78. https://doi.org/10.1037/h0077298
dc.relation.referencesGilbert, S. F. (2001). Ecological developmental biology: Developmental biology meets the real world. Developmental Biology, 233(1), 1–12. https://doi.org/10.1006/dbio.2001.0210
dc.relation.referencesGilbert, S. F. (2001). Ecological developmental biology: Developmental biology meets the real world. Developmental Biology, 233(1), 1–12. https://doi.org/10.1006/dbio.2001.0210
dc.relation.referencesGottlieb, G. (1991b). Experiential Canalization of Behavioral Development: Theory. Developmental Psychology, 27, (1), 4-13. https://doi.org/10.1037/0012-1649.27.1.4
dc.relation.referencesGottlieb, G., & Halpern, C. T. (2002). A relational view of causality in normal and abnormal development. Development and Psychopathology, 14, 421–435. https://doi.org/10.1017.S0954579402003024
dc.relation.referencesGottlieb, G., & Halpern, C. T. (2002). A relational view of causality in normal and abnormal development. Development and Psychopathology, 14, 421–435. https://doi.org/10.1017.S0954579402003024
dc.relation.referencesGuevara-Fiore, P. (2012). Early social experience significantly affects sexual behaviour in male guppies. Animal behaviour, 84(1), 191-195.. https://doi.org/10.1016/j.anbehav.2012.04.031
dc.relation.referencesGuevara-Fiore, P. (2012). Early social experience significantly affects sexual behaviour in male guppies. Animal behaviour, 84(1), 191-195.. https://doi.org/10.1016/j.anbehav.2012.04.031
dc.relation.referencesGutiérrez, G., & Domjan, M. (2011). Conditioning of sexual proceptivity in female quail: Measures of conditioned place preference. Behavioural Processes, 87(3), 268-273. https://doi.org/10.1016/j.beproc.2011.05.004
dc.relation.referencesGutiérrez, G., & Domjan, M. (2011). Conditioning of sexual proceptivity in female quail: Measures of conditioned place preference. Behavioural Processes, 87(3), 268-273. https://doi.org/10.1016/j.beproc.2011.05.004
dc.relation.referencesHolloway, K. S., & Domjan, M. (1993). Sexual approach conditioning: unconditioned stimulus factors. Journal of Experimental Psychology: Animal Behavior Processes, 19(1), 38-46. https://doi.org/10.1037/0097-7403.19.1.38
dc.relation.referencesHolloway, K. S., & Domjan, M. (1993). Sexual approach conditioning: unconditioned stimulus factors. Journal of Experimental Psychology: Animal Behavior Processes, 19(1), 38-46. https://doi.org/10.1037/0097-7403.19.1.38
dc.relation.referencesHolloway, K. S., & Domjan, M. (1993). Sexual approach conditioning: unconditioned stimulus factors. Journal of Experimental Psychology: Animal Behavior Processes, 19(1), 38-46. https://doi.org/10.1037/0097-7403.19.1.38
dc.relation.referencesHolloway, K. S., & Domjan, M. (1993). Sexual approach conditioning: unconditioned stimulus factors. Journal of Experimental Psychology: Animal Behavior Processes, 19(1), 38-46. https://doi.org/10.1037/0097-7403.19.1.38
dc.relation.referencesHolloway, K. S., & Domjan, M. (1993). Sexual approach conditioning: unconditioned stimulus factors. Journal of Experimental Psychology: Animal Behavior Processes, 19(1), 38-46. https://doi.org/10.1037/0097-7403.19.1.38
dc.relation.referencesLogan, C. A., & Johnston, T. D. (2007). Synthesis and separation in the history of “nature” and “nurture”. Developmental Psychobiology: The Journal of the International Society for Developmental Psychobiology, 49(8), 758-769. https://doi.org/10.1002/dev.20274
dc.relation.referencesMahometa, M. J., & Domjan, M. (2005). Classical conditioning increases reproductive success in Japanese quail, Coturnix japonica. Animal Behaviour, 69(4), 983-989. https://doi.org/10.1016/j.anbehav.2004.06.023
dc.relation.referencesMills, A. D., Crawford, L. L., Domjan, M., & Faure, J. M. (1997). The behavior of the Japanese or domestic quail Coturnix japonica. Neuroscience & Biobehavioral Reviews, 21(3), 261-281. https://doi.org/10.1016/s0149-7634(96)00028-0
dc.relation.referencesMonaghan, P. (2008). Early growth conditions, phenotypic development and environmental change. Philosophical Transactions of the Royal Society B: Biological Sciences, 363(1497), 1635-1645. https://doi.org/10.1098/rstb.2007.0011
dc.relation.referencesNash, S., & Domjan, M. (1991). Learning to discriminate the sex of conspecifics in male Japanese quail (Coturnix coturnix japonica): Tests of" biological constraints.". Journal of Experimental Psychology: Animal Behavior Processes, 17(3), 342.–353. https://doi.org/10.1037/0097-7403.17.3.342
dc.relation.referencesO'Connell, M. E., Reboulleau, C., Feder, H. H., & Silver, R. (1981). Social interactions and androgen levels in birds: I. Female characteristics associated with increased plasma androgen levels in the male ring dove (Streptopelia risoria). General and Comparative Endocrinology, 44(4), 454-463. https://doi.org/10.1016/0016-6480(81)90332-4
dc.relation.referencesOjeda, S. R., Urbanski, H. F., Katz, K. H., & Costa, M. E. (1988). Prostaglandin E2 releases luteinizing hormone-releasing hormone from the female juvenile hypothalamus through a Ca2+-dependent, calmodulin-independent mechanism. Brain research, 441(1-2), 339-351.
dc.relation.referencesOjeda, S. R., Urbanski, H. F., Katz, K. H., & Costa, M. E. (1988). Prostaglandin E2 releases luteinizing hormone-releasing hormone from the female juvenile hypothalamus through a Ca2+-dependent, calmodulin-independent mechanism. Brain research, 441(1-2), 339-351.
dc.relation.referencesOphir, A. G., & Galef Jr, B. G. (2004). Sexual experience can affect use of public information in mate choice. Animal Behaviour, 68(5), 1221-1227. https://doi.org/10.1016/j.anbehav.2003.12.023
dc.relation.referencesOphir, A. G., Persaud, K. N., & Galef Jr, B. G. (2005). Avoidance of relatively aggressive male Japanese Quail (Coturnix japonica) by sexually experienced conspecific females. Journal of Comparative Psychology, 119(1), 3.–7. https://doi.org/10.1037/0735-7036.119.1.3
dc.relation.referencesOttinger, M. A., & Brinkley, H. J. (1979a). Testosterone and sex related physical characteristics during the maturation of the male Japanese quail (Coturnix coturnix japonica). Biology of reproduction, 20(4), 905-909.
dc.relation.referencesOttinger, M. A., & Brinkley, H. J. (1979b). The ontogeny of crowing and copulatory behavior in Japanese quail (Coturnix coturnix japonica). Behavioural Processes, 4(1), 43-51.
dc.relation.referencesOttinger, M. A., & Brinkley, H. J. (1979b). The ontogeny of crowing and copulatory behavior in Japanese quail (Coturnix coturnix japonica). Behavioural Processes, 4(1), 43-51.
dc.relation.referencesPavlov, I. P., (1927). Conditioned Reflexes. (London: Oxford University Press), pp. 16-32
dc.relation.referencesPérez Manrique, T., & Gutierrez, G. (2006). Efectos de la experiencia social temprana en las preferencias sexuales de la codorniz japonesa (coturnix japonica). Acta Colombiana de Psicología, 9(2), 57-73.
dc.relation.referencesPersaud, K. N., & Galef Jr, B. G. (2005a). Eggs of a female Japanese quail are more likely to be fertilized by a male that she prefers. Journal of Comparative Psychology, 119(3), 251–256. https://doi.org/10.1037/0735-7036.119.3.251
dc.relation.referencesPersaud, K. N., & Galef Jr, B. G. (2005b). Female Japanese quail (Coturnix japonica) mated with males that harassed them are unlikely to lay fertilized eggs. Journal of Comparative Psychology, 119(4), 440–446. https://doi.org/10.1037/0735-7036.119.4.440
dc.relation.referencesPfaus, J. G. (1996). Frank A. Beach award: Homologies of animal and human sexual behaviors. Hormones and behavior, 30(3), 187-200.
dc.relation.referencesPolejack, A., & Tidon, R. (2007). Learning of courtship components in Drosophila mercatorum (Paterson & Wheller)(Diptera, Drosophilidae). Revista Brasileira de Entomologia, 51, 82-86.
dc.relation.referencesPuentes, M. (2016). Efectos transgeneracionales del aprendizaje temprano en un modelo aviar. (tesis de posgrado). Universidad Nacional de Colombia, Bogotá, Colombia.
dc.relation.referencesQian, Y., Chen, W., & Guo, B. (2020). Zing-Yang Kuo and behavior epigenesis based on animal experiments. Protein & Cell, 11(6), 387-390. https://doi.org/10.1007/s13238-018-0516-9
dc.relation.referencesRather, P. A., Herzog, A. E., Ernst, D. A., & Westerman, E. L. (2022). Effect of experience on mating behaviour in male Heliconius melpomene butterflies. Animal Behaviour, 183, 139-149. https://doi.org/10.1016/j.anbehav.2021.11.004
dc.relation.referencesRescorla, R. A. (1967). Pavlovian conditioning and its proper control procedures. Psychological review, 74(1), 71.
dc.relation.referencesRiters, L. V., Absil, P., & Balthazart, J. (1998). Effects of brain testosterone implants on appetitive and consummatory components of male sexual behavior in Japanese quail. Brain research bulletin, 47(1), 69-79. https://doi.org/10.1016/S0361-9230(98)00064-1
dc.relation.referencesRosenzweig, M. R., & Bennett, E. L. (1996). Psychobiology of plasticity: effects of training and experience on brain and behavior. Behavioural brain research, 78(1), 57-65. https://doi.org/10.1016/0166-4328(95)00216-2
dc.relation.referencesSachs, B. D. (2007). A contextual definition of male sexual arousal. Hormones and Behavior, 51(5), 569-578. https://doi.org/10.1016/j.yhbeh.2007.03.011
dc.relation.referencesSakata, J. T., Gupta, A., Chuang, C. P., & Crews, D. (2002). Social experience affects territorial and reproductive behaviours in male leopard geckos, Eublepharis macularius. Animal Behaviour, 63(3), 487-493. https://doi.org/10.1006/anbe.2001.1952
dc.relation.referencesSchulz, K. M., & Sisk, C. L. (2006). Pubertal hormones, the adolescent brain, and the maturation of social behaviors: lessons from the Syrian hamster. Molecular and cellular endocrinology, 254, 120-126. https://doi.org/10.1016/j.mce.2006.04.025
dc.relation.referencesSchumacher, M., & Balthazart, J. (1983). The effects of testosterone and its metabolites on sexual behavior and morphology in male and female Japanese quail. Physiology & behavior, 30(3), 335-339. https://doi.org/10.1016/0031-9384(83)90135-X
dc.relation.referencesSeiwert, C. M., & Adkins-Regan, E. (1998). The foam production system of the male Japanese quail: characterization of structure and function. Brain Behavior and Evolution, 52(2), 61-80. https://doi.org/10.1159/000006553
dc.relation.referencesSeiwert, C. M., & Adkins-Regan, E. (1998). The foam production system of the male Japanese quail: characterization of structure and function. Brain Behavior and Evolution, 52(2), 61-80. https://doi.org/10.1159/000006553
dc.relation.referencesSilva, K. M., & Timberlake, W. (1998). The organization and temporal properties of appetitive behavior in rats. Animal Learning & Behavior, 26(2), 182-195.
dc.relation.referencesSisk, C. L., & Foster, D. L. (2004). The neural basis of puberty and adolescence. Nature neuroscience, 7(10), 1040-1047. https://doi.org/10.1038/nn1326
dc.relation.referencesTaziaux, M., Cornil, C. A., & Balthazart, J. (2004). Aromatase inhibition blocks the expression of sexually-motivated cloacal gland movements in male quail. Behavioural processes, 67(3), 461-469. https://doi.org/10.1016/j.beproc.2004.07.007
dc.relation.referencesThompson, R., Goodson, J., Ruscio, M., & Adkins-Regan, E. (1998). Role of the archistriatal nucleus taeniae in the sexual behavior of male Japanese quail (Coturnix japonica): a comparison of function with the medial nucleus of the amygdala in mammals. Brain Behavior and Evolution, 51(4), 215-229. https://doi.org/10.1159/000006539
dc.relation.referencesWest-Eberhard, M. J. (1989). Phenotypic Plasticity and the Origins of Diversity. Annual Review of Ecology and Systematics, 20, 249–278.
dc.relation.referencesWest-Eberhard, M. J. (2003). Developmental plasticity and evolution. Oxford University Press.
dc.relation.referencesWhite, D. J., & Galef Jr, B. G. (1999). Mate choice copying and conspecific cueing in Japanese quail, Coturnix coturnix japonica. Animal Behaviour, 57(2), 465-473. https://doi.org/10.1006/anbe.1998.1015Wild, J. M., & Balthazart, J. (2013). Neural pathways mediating control of reproductive behavior in male Japanese quail. Journal of Comparative Neurology, 521(9), 2067-2087. https://doi.org/10.1002/cne.23275
dc.relation.referencesWoodson, J. C. (2002). Including ‘learned sexuality’in the organization of sexual behavior. Neuroscience & Biobehavioral Reviews, 26(1), 69-80. https://doi.org/10.1016/s0149-7634(01)00039-2
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.subject.proposalConducta sexual
dc.subject.proposalDesarrollo
dc.subject.proposalExperiencias tempranas
dc.subject.proposalAprendizaje
dc.subject.proposalCondicionamiento sexual
dc.subject.proposalCoturnix japonica
dc.subject.proposalSexual behavior
dc.subject.proposalDevelopment
dc.subject.proposalEarly experiencies
dc.subject.proposalLearning
dc.subject.proposalSexual conditioning
dc.title.translatedEarly social exposure, learning, and development of sexual behavior in japanese quail (coturnix japonica)
dc.type.coarhttp://purl.org/coar/resource_type/c_bdcc
dc.type.coarversionhttp://purl.org/coar/version/c_ab4af688f83e57aa
dc.type.contentText
dc.type.redcolhttp://purl.org/redcol/resource_type/TM
oaire.accessrightshttp://purl.org/coar/access_right/c_abf2
dcterms.audience.professionaldevelopmentAdministradores
dcterms.audience.professionaldevelopmentBibliotecarios
dcterms.audience.professionaldevelopmentConsejeros
dcterms.audience.professionaldevelopmentEstudiantes
dcterms.audience.professionaldevelopmentGrupos comunitarios
dcterms.audience.professionaldevelopmentInvestigadores
dcterms.audience.professionaldevelopmentMaestros
dcterms.audience.professionaldevelopmentMedios de comunicación
dcterms.audience.professionaldevelopmentPadres y familias
dcterms.audience.professionaldevelopmentPersonal de apoyo escolar
dcterms.audience.professionaldevelopmentProveedores de ayuda financiera para estudiantes
dcterms.audience.professionaldevelopmentPúblico general
dcterms.audience.professionaldevelopmentReceptores de fondos federales y solicitantes
dcterms.audience.professionaldevelopmentResponsables políticos


Archivos en el documento

Thumbnail
Nombre:
1018475349.2023.pdf
Tamaño:
1.987Mb
Formato:
PDF
Descripción:
Tesis de Maestría en Psicología
Descargar

Este documento aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del documento

Reconocimiento 4.0 InternacionalEsta obra está bajo licencia internacional Creative Commons Reconocimiento-NoComercial 4.0.Este documento ha sido depositado por parte de el(los) autor(es) bajo la siguiente constancia de depósito