Abstract
This chapter builds on the excellent review of avian song development by [Bottjer and Arnold (1986)] that appeared in an earlier volume of this series ([Blass, 1986]). We first summarize the knowledge and perspectives on the neurobiology of song development and production of that time. We then present an overview of the major advances that have occurred since the earlier review, and finish with a description of the research avenues that we feel are likely to yield significant advances in our understanding of the neurobiology of bird song
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References
Aamodt, S. M., Kozlowski, M. R., Nordeen, E.J., & Nordeen, K. W. (1992). Distribution and developmental change in [3H] MK801 binding within zebra finch song nuclei. Journal of Neurobiology, 23, 997–1005
Aamodt, S. M., Nordeen, E.J. & Nordeen, K. W. (1996). Blockade of NMDA receptors during song model exposure impairs song development in juvenile zebra finches. Neurobiology of Learning and Memory, 65, 91–98
Adkins-Regan, E., & Ascenzi, M. (1987). Social and sexual behaviour of male and female zebra finches treated with oestradiol during the nestling period. Animal Behaviour, 35, 1100–1112
Adkins-Regan, E., Abdelnabi, M., Mobarak, M., & Ottinger, M. A. (1990). Sex steroid levels in developing and adult male and female zebra finches (Poephila guttata). General and Comparative Endocrinology, 78, 93–109
Adkins-Regan, E., Mansukhani, V., Seiwert, C., & Thompson, R. (1994). Sexual differentiation of brain and behavior in the zebra finch: Critical periods for effects of early estrogen treatment. Journal of Neurobiology, 25, 865–877
Adret, P. (1993). Operant conditioning, song learning and imprinting to taped song in the zebra finch. Animal Behaviour, 46, 149–159
Airey, D. C., & DeVoogd, T. J. (2000). Variation in song complexity and HVC volume are significantly related in zebra finches. Neuroreport, 10, 2339–2344
Airey, D. C., Buchanan, K. L., Catchpole, C.K. Szekely, T., & DeVoogd, T. J. (2000). Song complexity, sexual selection and a song control nucleus (HVC) in the brains of European sedge warblers. Journal of Neurobiology, 43, 244–253
Airey, D. C, Castillo-Juarez, H., Casella, G., Pollak, E. J., & DeVoogd, T.J. (2000). Variation in the volume of zebra finch song control nuclei is heritable: Developmental and evolutionary implications. Proceedings of the Royal Society,Series B, 267, 2099–2104
Airey, D. C., Kroodsma, D. E., & DeVoogd, T. J. (2000). Learning a larger song repertoire increases spine density in a songbird telencephalic control nucleus. Neurobiology of Learning and Memory, 73, 274–281
Akutagawa, E., & Konishi, M. (1998). Transient expression and transport of brain-derived neurotrophic factor in the male zebra finch’s song system during vocal development. Proceedings of the National Academy of Sciences of the USA, 95, 11429–11434
Arnold, A. P, (1996), Genetically triggered sexual differentiation of brain and behavior. Hormones and Behavior, 30, 495–515
Arnold, A. P. (1997). Sexual differentiation of the zebra finch song system: Positive evidence, negative evidence, null hypotheses, and a paradigm shift. Journal of Neurobiology, 33, 572–584
Arnold, A. P. Sc Saltiel, A. (1979). Sexual difference in pattern of hormone accumulation in the brain of a songbird. Science, 205, 702–704
Arnold, A. P., Nottebohm, F., & Pfaff, D. W. (1976). Hormone accumulating cells in vocal control and other brain regions of the zebra finch (Poephila guttata). Journal of Comparative Neurology, 165, 487–512
Arnold, A. E, Wade, J., Grisham, W., & Jacobs, E. C. (1996). Sexual differentiation of the brain in songbirds. Developmental Neuroscience, 18, 124–136
Ball, G. F. (1993). The neural integration of environmental information by seasonally breeding birds. American Zoologist, 33, 185–199
Ball, G. F., & Gentner, T. Q. (1998). They’re playing our song: Gene expression and birdsong perception. Neuron, 21, 271–274
Ball, G. E, Casto, J. M., & Bernard, D.J. (1994). Sex differences in the volume of avian song control nuclei Comparative studies and the issue of brain nucleus delineation. Psychoneunnendocrinlogy, 19, 485–504
Baptista, L. F., Bell, A., & Trail, P. W. (1993). Song learning and production in the white-crowned sparrow:Parallels with sexual imprinting. Netherlands Journal of Zoology, 43, 17–33
Basham, M. E., Nordeen, E. J., & Nordeen, K. W. (1996). Blockade of NMDA receptors in the anterior forebrain impairs memory acquisition in the zebra finch. Neurobiology of Learning and Memory, 66, 295–304
Basham, M. E., Sohrabji, F., Singh, T. D., Nordeen, E. J., Sc Nordeen, K. W. (1999). Developmental regulation of NMDA receptor 2B subunit mRNA and ifenprodil binding in the zebra finch anterior forebrain. Journal of Neurobiology, 39, 155–167
Benton, S., Cardin, J. A., & DeVoogd, T. J. (1998). Lucifer yellow filling of Area X-projecting neurons in the high vocal center of female canaries. Brain Research,799, 138–147
Benton, S., Nelson, D. A., Marier, P., Sc DeVoogd, T. J. (1998). Anterior forebrain pathway mediates seasonal song expression in adult male white-crowned sparrows (Zonotrichia leucophrys). Behavioural Brain Research, 96, 135–150
Bernard, D. J., & Ball, G. F. (1997). Photoperiodic condition modulates the effects of testosterone on song control nuclei volumes in male European starlings. General and Comparative Endocrinology, 105, 276–283
Bernard, D. J., Wilson, F. E., & Ball, G. F. (1997). Testis-dependent and -independent effects of photo-period on volumes of song control nuclei in American tree sparrows (Spizella arborea). Brain Research, 760, 263–169
Blass, E. M. (Ed.). (1986). Handbook of behavioral neurobiology, Volume 8, Developmental psychobiology and developmental neurobiology New York: Plenum Press
Bock, J., & Braun, K. (1998). Differential emotional experience leads to pruning of dendritic spines in the forebrain of domestic chick. Neural Plasticity, 6, s17–27
Bock, J., & Braun, K (1999). Blockade of Nmethyl-o-aspartate receptor activation suppresses learning-induced synaptic elimination. Proceedings of the National Academy of Sciences of the USA, 96, 2485–2490
Boettiger, C. A., Sc Doupe, A. J. (1998). Intrinsic and thalamic excitatory inputs onto songbird LAMN neurons differ in their pharmacological and temporal properties. Journal of Neurophysiology, 79, 26152–628
Bottjer, S. W., & Arnold, A. P. (1986). The ontogeny of vocal learning in songbirds. In E. M. Blass (Ed.), Handbook of behavioral neurobiology, Volume 8, Developmental psychobiology and developmental neurobiology (pp. 129–161). New York: Plenum Press
Bottjer, S. W., & Hewer, S. J. (1992). Castration and antisteroid treatment impair vocal learning in male zebra finches. Journal of Neurobiology, 23, 337–353
Bottjer, S. W., & Sengelaub, D. R (1989). Cell death during development of a forebrain nucleus involved with vocal learning in zebra finches. Journal of Neurobiology, 20, 609–618
Bottjer, S. W., Miesner, E., & Arnold, A. P. (1984). Forebrain lesions disrupt development but not maintenance of song in passerine birds, Science, 224, 901–903
Bottjer, S. W., Glaessner, S. L., & Arnold A. P. (1985). Ontogeny of brain nuclei controlling song learning and behavior in zebra finches. Journal of Neuroscience, 5, 1556–1562
Bottjer, S. W., Halsema, K. A., Brown, S. A., & Miesner, E. A. (1989). Axonal connections of a forebrain nucleus involved with vocal learning in zebra finches. Journal of Comparative Neurology, 279, 312–326
Brenowitz, E. A. (1991). Altered perception of species-specific song by female birds after lesions of a forebrain nucleus. Science, 251, 303–305
Brenowitz, E. A. (1997). Comparative approaches to the avian song system. Journal of Neurobiology, 33, 517–531
Brenowitz, E. A., & Arnold, A. P. (1986). Interspecific comparisons of the size of neural song control regions and song complexity in duetting birds: Evolutionary implications. Journal of Neuroscience, 6, 2875–2879
Brenowitz, E. A., Arnold, A. P., Sc Levin, R. A. (1985). Neural correlates of female song in tropical duetting birds. Brain Research,343, 104–112
Brenowitz, E. A., Nails, B., Wingfield, J. C., & Kroodsma, D. E. (1991). Seasonal changes in avian song nuclei without seasonal changes in song repertoire. Journal of Neuroscience, 11, 1367–1374
Brenowitz, E. A., Lent, K., & Kroodsma, D. E. (1995). Brain space for learned song in birds develops independently of song learning. Journal of Neuroscience, 15, 6281–6286
Buchanan, K. L., & Catchpole, C. K. (1997). Female choice in the sedge warbler Acrocephalus schoenobaenvs Multiple cues from song and territory quality. Proceedings of the Royal Society of London, Series B, 264, 521–526
Canady, R. A., Kroodsma, D. E., & Nottebohm, F. (1984). Population differences in complexity of a learned skill are correlated with the brain space involved. Proceedings of the National Academy of Sciences of the USA,Si, 6232–6234
Chaiken, M., Bohner, J., & Marier, P. (1993). Song acquisition in European starlings (Sturnus vulgari.$): A comparison of the songs of live-tutored, tape-tutored, untutored and wild-caught males. Animal Behaviour, 46, 1079–1090
Chew, W. J., Vicario, D. S., Sc Nottebohm, F. (1996). A large capacity memory system that recognizes the calls and songs of individual birds. Proceedings of the National Academy of Sciences of the USA, 93, 1950–1955
Clayton, N. S. (1987). Song tutor choice in zebra finches. Animal Behaviour, 35, 714–722
Clemmons, J. R. (1995). Development of a selective response to an adult vocalization in nestling black-capped chickadees. Behaviour, 132, 1–20
Glower, R. P., Nixdorf, B. E., & DeVoogd, T. J. (1989). Synaptic plasticity in the hypoglossal nucleus of female canaries: Structural correlates of season, hemisphere and testosterone treatment. Behavioral Neural Biology, 52, 63–77
Collins, C. E., Airey, D. C., Guzman, J. R., Tremper, K. A,. & DeVoogd, T. J. Group-raised, song-deprived zebra finches exhibit abnormal song structure, but normal social behavioral development. Journal of Comparative Psychology, under revision
Coffins, S. A., Hubbard, C., & Houtman, A. M. (1994). Female mate choice in the zebra finch: The effect of male beak colour and male song. Behavioral Ecology and Sociobiology, 35, 21–25
Cynx, J., & Nottebohm, F. (1992) Role of gender, season and familiarity in discrimination of conspecific song by zebra finches. Proceedings of the National Academy of Sciences of the USA, 89, 1368–1371
Dave, A. S., Yu, A. C., & Margoliash, D. (1998). Behavioral state modulation of auditory activity in a vocal motor system. Science, 282, 2250–2254
Del Negro, C., Gahr, M., Leboucher, G., Sc Kreutzer, M. (1998). The selectivity of sexual responses to song displays: Effects of partial chemical lesion of the HVC in female canaries. Behavioural Brain Research, 96, 151–159
DeVoogd, T. J. (1991). Endocrine modulation of the development and adult function of the avian song system. Psychoneuroendocrinology, 16, 41–66
DeVoogd, T. J. (1994). Interactions between endocrinology and learning in the avian song system. Annals of the New York Academy of Sciences,743, 19–43
DeVoogd, T. J., & Nottebohm, F. (1981a). Sex differences in dendritic morphology of a song control nucleus in the canary: A quantitative Golgi study. Journal of Comparative Neurology, 196, 309–316
DeVoogd, T. J., & Nottebohm, F. (1981b). Gonadal hormones induce dendritic growth in the adult brain. Science, 214, 202–204
DeVoogd, T. J. & Szekely, T. (1998). Causes of avian song: Using neurobiology to integrate proximal and ultimate levels of analysis. In I. Pepperberg, A. Kamil, & R Bahia (Eds.), Animal cognition in nature (pp. 337–380), New York: Academic Press
DeVoogd, T.J., Nixdorf, B., & Nottebohm, F. (1985). Formation of new synapses related to acquisition of a new behavior. Brain Research, 329, 304–308
DeVoogd, T. J., Brenowitz, E. A., & Arnold, A. P. (1988). Small sex differences in song control dendrites are associated with minimal differences in song capacity. Journal of Neurobiology, 19, 199–209
DeVoogd, T.J., Krebs, J. R., Healy, S. D., & Purvis, A. (1993). Evolutionary correlation between repertoire size and a brain nucleus amongst passerine birds. Proceedings of the Royal Society of London, Series B, 254, 75–82
DeVoogd, T. J., Houtman, A., & Falls, B. (1995). White-throated sparrow morphs that differ in song production rate also differ in the anatomy of some song-related brain areas. Journal of Neurobiology, 28, 202–213
Dittrich, F., Feng, Y., Metzdorf, R, & Gahr, M. (1999). Estrogen-inducible, sex-specific expression of brain-derived neurotrophic factor mRNA in a forebrain song control nucleus of the juvenile zebra finch. Proceedings of the National Academy of Sciences of the USA, 96, 8241–8246
Doupe, A. J. (1997). Song-and order-selective neurons in the songbird anterior forebrain and their emergence during vocal development. Journal of Neuroscience, 17, 1147–1167
Doupe, A.J., & Konishi, M. (1991). Song-selective auditory circuits in the vocal control system of the zebra finch. Proceedings of the National Academy of Sciences of the USA, 96, 11339–11343
Dubnau, J., & Tully, T. (1998) Gene discovery in Drosophila: New insights for learning and memory. Annual Review of Neuroscience, 21, 407–444
Eales, L. A. (1985). Song learning in zebra finches: Some effects of song model availability on what is learnt and when. Animal Behaviour, 33, 1293–1300
Eens, M. (1997). Understanding the complex song of the European starling: An integrated ethological approach. Advances in the Study of Behavior, 26, 355–434
Foster, E. F. & Bottjer, S. W. (1998). Axonal connections of the high vocal conter and surrounding cortical regions in juvenile and adult male zebra finches. Journal of Comparative Neurology, 397, 118–138
Foster, E. F., Mehta, R. P., & Bottjer, S. W. (1997). Axonal connections of the medial magnocellular nucleus of the anterior neostriatum in zebra finches. Journal of Comparative Neurology, 382, 364–381
Gahr, M., & Konishi, M. (1988). Developmental changes in estrogen-sensitive neurons in the forebrain of the zebra finch. Proceedings of the National Academy of Sciences of the USA, 85, 7380–7383
Gahr, M., Sc Kosar, E. (1996). Identification, distribution and developmental changes of a melatonin binding site in the song control system of the zebra finch. Journal of Comparative Neurology, 367, 308–318
Gahr, M., & Metzdorf, R (1999). The sexually dimorphic expression of androgen receptors in the song nucleus hyperstriatalis ventrale pars caudale of the zebra finch develops independently of gonadal steroids. Journal of Neuroscience, 19, 2628–2636
Gahr, M., Sonnenshein, E., Sc Wickler, W. (1998). Sex difference in the size of the neural song control regions in a dueling songbird with similar song repertoire size of males and females. Journal of Neuroscience, 18, 1124–1131
Gentner, T. Q., & Hulse, S. H. (1998). Perceptual mechanisms for individual vocal recognition in European starlings, Sturnus vulgaris. Animal Behaviour, 56, 579–594
Grisham, W., & Arnold, A. P. (1995). A direct comparison of the masculinizing effects of testosterone, androstenedione, estrogen, and progesterone on the development of the zebra finch song system. Journal of Neurobiology, 26, 163–170
Gulledge, C. C., & Deviche, P. (1998). Photoperiod and testosterone independently affect vocal control region volumes in adolescent male songbirds. Journal of Neurobiology, 36, 550–558
Gurney, M. (1981). Hormonal control of cell form and number in the zebra finch song system. Journal of Neuroscience, 1, 658–673
Gurney, M. E., & Konishi, M. (1980). Hormone induced sexual differentiation of brain and behavior in zebra finches. Science, 208, 1380–1383
Hamilton, K. S., King, A. P., Sengelaub, D. R., & West, M. J. (1997). A brain of her own: A neural correlate of song assessment in a female songbird. Neurobiology of Learning and Memory, 68, 325–332
Harding, C. E (1986). The role of androgen metabolism in the activation of male behavior. Annals of the New York Academy of Sciences, 474, 371–378
Harding, C. F., Barclay, S. R., & Waterman, S. A. (1998). Changes in catecholamine levels and turnover rates in hypothalamic, vocal control, and auditory nuclei in male zebra finches during development. Journal of Neurobiology, 34, 329–346
Harry, J., Koopman, P., Brennan, F., Graves, J., & Renfree, M. (1995). Widespread expression of the testis-determining gene SRY in a marsupial. Nature Genetics, 11, 347--349
Hasselquist, D., Bertsch, S., & Von-Schantz, T. (1996). Correlation between male song repertoire, extra-pair paternity and offspring survival in the great reed warbler. Nature, 381, 229–232
Hausberger, M., Richard-Yris, M.-A., Henry, L., Lepage, L., & Schmidt, I. (1995). Song sharing reflects the social organization in a captive group of European starlings (Sturnus vulgatis). Journal of Comparative Psychology, 109, 222–241
Hessler, N. A., & Doupe, A. J. (1999). Social context modulates singing-related neural activity in the songbird forebrain. Nature Neuroscience, 2, 209–211
Hidalgo, A., Barami, K., Iverson, K., & Goldman, S. A. (1995). Estrogens and non-estrogenic ovarian influences combine to promote the recruitment, and decrease the turnover of new neurons in the adult female canary brain. Journal of Neurobiology, 27, 470–487
Hill, K M., & DeVoogd, T. J. (1991). Decreased daylength results in dendritic shrinkage and loss of dendritic spines in a brain nucleus involved in seasonal production of song. Behavioral and Neural Biology, 56, 240–250
Houtman, A. (1992). Female zebra finches choose extra-pair copulations with genetically attractive males. Proceedings of the Royal Society of London,Series B, 249, 3–6
Hultsch, H., Schleuss, E, & Todt, D. (1999). Auditory—visual stimulus pairing enhances perceptual learning in a songbird. Animal Behaviour, 58, 143–149
Iyengar, S., Viswanathan, S. S., & Bottjer, S. W. (1999) Development of topography within song control circuitry of zebra finches during the sensitive period for song learning. Journal of Neuroscience, 19, 6037–6057
Jacobs, E. C., Grisham, W., & Arnold, A. P. (1995). Lack of a synergistic effect between estradiol and dihydrotestosterone in the masculinization of the zebra finch song system. Journal of Neurobiology, 27, 513–519
Janata, P., Sc Margoliash, D. (1999). Gradual emergence of song selectivity in sensorimotor structures of the male zebra finch song system. Journal of Neuroscience, 19, 5108–5118
Jarvis, E. D., & Nottebohm, F. (1997). Motor-driven gene expression. Proceedings of the National Academy of Sciences of the USA, 94, 4097–4102
Jarvis, E. D., Schwabl, H., Ribeiro, S., Sc Mello, C. V. (1997). Brain gene regulation by territorial singing behavior in freely ranging songbirds. Neuroreport,3, 2073–2077
Jarvis, E. D., Scharff, C., Grossman, M. R., Ramos, J. A., & Nottebohm, F. (1998). For whom the bird sings: Context-dependent gene expression. Neuron, 21, 775–788
Jin, H., & Clayton, D. F. (1997). Localized changes in immediate-early gene regulation during sensory and motor learning in zebra finches. Neuron, 19, 1049–1059
Johnson, F., Sablan, M. M., & Bottjer, S. W. (1995). Topographic organization of a forebrain pathway involved with vocal learning in zebra finches. Journal of Comparative Neurology, 358, 260–278
Johnson, F., Hohmann, S. E., DiStefano, P. S., Sc Bottjer, S. W. (1997). Neurotrophins suppress apoptosis induced by deafferentation of an avian motor-cortical region. Journal of Neuroscience, 17, 2101–2111
Kirn, J. R., & DeVoogd, T. J. (1989). The genesis and death of vocal control neurons during sexual differentiation in the zebra finch. Journal of Neuroscience, 9, 3176–87
Kirn, J. R., & Schwabl, H. (1997). Photoperiod regulation of neuron death in the adult canary. Journal of Neurobiology, 33, 223–231
Kirn, J. R., Clower, R. P., Kroodsma, D. E., & DeVoogd, T. J. (1989). Song-related brain regions in the red-winged blackbird are affected by sex and season but not repertoire size. Journal of Neurobiology, 20, 139–163
Kittelberger, J. M., & Mooney, R. (1999). Lesions of an avían forebrain nucleus that disrupt song development alter synaptic connectivity and transmission in the vocal premotor pathway. Journal of Neuroscience, 19, 9385–9398
Konishi, M. (1965). The role of auditory feedback in the control of vocalization in the white-crowned sparrow. Zeitschrift für Tierpsychologie, 22, 584–599
Konishi, M., Sc Akutagawa, E. (1985). Neuronal growth, atrophy and death in a sexually dimorphic song nucleus in the zebra finch brain. Nature, 315, 145–147
Konishi, M., & Akutagawa, E. (1988). A critical period for estrogen action on neurons of the song control system in the zebra finch, Proceedings of the National Academy of Sciences of the USA, 85, 7006–7007
Korsia, S., & Bottjer, S. W. (1991). Chronic testosterone treatment impairs vocal learning in male zebra finches during a restricted period of development. Journal of Neuroscience, 11, 2362–2371
Kroodsma, D. E. (1996). Ecology of passerine song development. In D. E. Kroodsma & E. H. Miller (Eds.), Ecology and evolution of acoustic communication in birds (pp. 3–19), Ithaca, NY: Cornell University Press
Kroodsma, D. E., Sc Byers, B. E. (1991). The functions(s) of bird song. American Zoologist, 31, 318–328
Leonard, M. L., Horn, A. G., Brown, C. R., & Fernandez, N.J. (1997). Parent—offspring recognition in tree swallows, Tachycineta bicolor. Animal Behaviour, 54, 1107–1116
Lewicki, M. S., & Arthur, B. J. (1996). Hierarchical organization of auditory temporal context sensitivity. Journal of Neuroscience, 16, 6987–6998
Lim, D., & Kim, C. (1997). Emerging auditory response interactions to harmonic complexes in field L of the zebra finch. Auric Nasus Larynx,24, 227–232
MacDougall-Shackleton, S. A, Hulse, S. H., & Ball, G. F. (1998a). Neural bases of song preferences in female zebra finches (Taeniopygia guttata). NeuroReport, 9, 3047–3052
MacDougall-Shackleton, S. A., Hulse, S. H., Sc Ball, G. F. (1998b). Neural correlates of singing behavior in male zebra finches (Taeniopygia guttata). Journal of Neurobiology, 36, 421–430
Maekawa, M., & Uno, H. (1996). Difference in selectivity to song note properties between the vocal nuclei of the zebra finch. Neuroscience Letters, 218, 123–126
Margoliash, D. (1983). Acoustic parameters underlying the responses of song-specific neurons in the white-crowned sparrow. Journal of Neuroscience, 3, 1039–1057
Margoliash, D. (1997). Functional organization of forebrain pathways for song production and perception. Journal of Neurobiology, 33, 671–693
Margoliash, D., & Fortune, E. S. (1992). Temporal and harmonic combination-sensitive neurons in the zebra finch’s HVc. Journal of Neuroscience, 12, 4309–4326
Marier, P. (1970). A comparative approach to vocal learning: Song development in white-crowned sparrows. Journal of Comparative and Physiological Psychology, 71/2, 1–25
Marler, P. (1976). Sensory templates in species-specific behavior. In J. Fentress (Ed.), Simpler networks and behavior (pp. 314–329). Sunderland, MA: Sinauer
Marier, P, (1984). Song learning: Innate species differences in the learning process. In P. Marier & H. S. Terrace (Eds.), The biology of learning (pp. 289–309). Berlin: Springer-Verlag
Mader, P. (1990). Song learning: The interface between behaviour and neuroethology. Philosophical Transactions of the Royal Society of London, Series B, 329, 109–114
Marier, P. (1991). Differences in behavioural development in closely related species: Birdsong. In P. Bateson (Ed.), The development and integration of behaviour: Essays in honour of Robert Hinde (pp. 41–70). Cambridge- Cambridge University Press
Marier, P., & Peters, S. (1982). Long-term storage of learned birdsongs prior to production. Animal Behaviour, 30, 479–482
Marler, P., & Peters, S. (1989). Species differences in auditory responsiveness in early vocal learning. In R. J. Dooling Sc S. H. Hulse (Eds.), The comparative psychology of audition: Perceiving complex sounds (pp. 243–273). Hillsdale, NJ: Erlbaum
Marier, P., & Sherman, V. (1983). Song structure without auditory feedback: Emendations of the auditory template hypothesis. Journal of Neuroscience, 3, 517–531
McCasland, J. S., & Konishi, M. (1981). Interaction between auditory and motor activities in an avian song control nucleus. Proceedings of the National Academy of Sciences of the USA, 78, 7815–7819
Mello, C. V., & Clayton, D. F. (1994). Song-induced ZENK gene expression in auditory pathways of songbird brain and its relation to the song control system. Journal of Neuroscience, 14, 6652–6666
Mello, C. V., & Ribeiro, S. (1998). ZENK protein regulation by song in the brain of songbirds. Journal of Comparative Neurology, 393, 426–438
Mello, C. V., Nottebohm, E, & Clayton, D. F. (1995). Repeated exposure to song leads to a rapid and persistent decline in an immediate early gene’s response to that song in the zebra finch tetencephalon. Journal of Neuroscience, 15, 6919–6925
Mello, C. V., Vicario, D. S., Sc Clayton, D. F. (1992). Song presentation induces gene expression in the songbird forebrain. Proceedings of the National Academy of Sciences of the USA, 89, 6818–6822
Mello, C. V., Vates, G. E., Okuhata, S., & Nottebohm, F. (1998). Descending auditory pathways in the adult male zebra finch (Taeniopygia guttata). Journal of Comparative Neurology, 395, 137–160
Miller, D. B. (1979). The acoustic basis of mate recognition by female zebra finches (Taeniopygia guttata) Animal Behaviour, 27, 376–380
Mooney, R. (1992). Synaptic basis for developmental plasticity in a birdsong nucleus. Journal of Neuroscience, 12, 2464–2477
Mooney, R., & Konishi, M. (1991). Two distinct inputs to an avian song nucleus activate different glutamate receptor subtypes on individual neurons. Proceedings of the National Academy of Sciences of the USA, 88, 4075–4079
Morrison, R. G., & Nottebohm, E (1993). Role of a telencephalic nucleus in the delayed song learning of socially isolated zebra finches. Journal of Neurobiology, 24, 1045–1064
Morton, E. S. (1996). A comparison of vocal behavior among tropical and temperate passerine birds. In D. E. Kroodsma & E. H. Miller (Eds.), Ecology and evolution of acoustic communication in birds (pp. 258268). Ithaca, NY: Cornell University Press
Naguib, M., & Todt, D. (1998). Recognition of neighbors’ song in a species with large and complex song repertoires: The thrush nightingale. Journal of Avian Biology, 29, 155–160
Nelson, D. A. (1997). Social interaction and sensitive phases for song learning: a critical review. In C. T. Snowdon & M. Hausberger (Eds.), Social interaction and development (pp. 7–22). Cambridge: Cambridge University Press
Nelson, D. A. (1998). External validity and experimental design: The sensitive phase for song learning. Animal Behaviour, 56, 487–491
Nelson, D. A-, Marier, P., & Morton, M. L. (1996). Overproduction in song development: An evolutionary correlate with migration. Animal Behaviour, 51, 1127–1140
Nelson, D. A., Marier, P. Soha, J. A., & Fullerton, A. L. (1997). The timing of song memorization differs in males and females: A new assay for avian vocal learning. Animal Behaviour, 54, 587–597
Newman, S. W. (1999). The medial extended amygdala in male reproductive behavior: A node in the mammalian social behavior network. Annals of the New York Academy of Sciences, 877, 242–257
Nixdorf-Bergwieler, B. E. (1996). Divergent and parallel development in volume sizes of telencephalic song nuclei in male and female zebra finches. Journal of Comparative Neurology, 375, 445–456
Nixdorf-Bergweiler, B. E., Lips, M. B., & Heinemann, U. (1995). Electrophysiological and morphological evidence for a new projection of LMAN neurones towards area X. Neuroreport,6, 1729–1732
Nixdorf-Bergweiler, B. E., Wallhausser-Franke, E., & DeVoogd, T. J. (1995). Regression in neuronal structure during song learning in songbirds. Journal of Neurobiology, 27, 204–215
Nordeen, E. J., & Nordeen, K W. (1988). Sex and regional differences in the incorporation of neurons born during song learning in zebra finches. Journal of Neuroscience, 8, 2869–2874
Nordeen, E. J., & Nordeen, K W. (1989). Estrogen stimulates the incorporation of new neurons into avian song nuclei during adolescence. Developmental Brain Research, 49, 27–32
Nordeen, E. J., & Nordeen, K. W. (1996). Sex difference among nonneuronal cells precedes sexually dimorphic neuron growth and survival in an avian song control nucleus. Journal of Neurobiology, 30, 531–542
Nordeen, E.J., Nordeen, K. W., & Arnold, A. P. (1987). Sexual differentiation of androgen accumulation in the zebra finch brain through selective cell loss and addition. Journal of Comparative Neurology, 259, 393–399
Nordeen, E. J., Grace, A., Burek, M. J., & Nordeen, K. W. (1992). Sex-dependent loss of projection neurons involved in avian song learning. Journal of Neurobiology, 23, 671–679
Nordeen, E. J., Voelkel, L., & Nordeen, K. W. (1998). Fibroblast growth factor-2 stimulates cell proliferation and decreases sexually dimorphic cell death in an avian song control nucleus. Journal of Neurobiology, 37, 573–581
Nordeen, K W., & Nordeen, E. J. (1997). Anatomical and synaptic substrates for avian song learning. Journal of Neurobiology, 33, 532–548
Nordeen, K. W., Nordeen, E. J., & Arnold, A. P. (1986). Estrogen establishes sex differences in androgen accumulation in zebra finch brain. Journal of Neuroscience, 6, 734–738
Nordeen, K W., Nordeen, E. J., & Arnold, A. P. (1987). Estrogen accumulation in zebra finch song control nuclei: Implications for sexual differentiation and adult activation of song behavior. Journal of Neurobiology, 18, 569–582
Nottebohm, F. (1980). Testosterone triggers growth of brain vocal control nuclei in adult female canaries. Brain Research, 189, 429–437
Nottebohm, F. (1981). A brain for all seasons: Cyclical anatomical changes in song-control nuclei of the canary brain. Science, 214, 1368–1370
Nottebohm, F. (1987). Plasticity in adult avian central nervous system: Possible relation between hormones, learning and brain repair. In Plum, F. (Ed.), Handbook of physiology, Section 1, The nervous system. Part V, Higher functions of the brain, Part 1 (pp. 85–108). Bethesda, MD: American Physiology Society
Nottebohm, F., & Arnold, A. P. (1976). Sexual dimorphism in vocal control areas of the song bird brain. Science, 194, 211–213
Nottebohm, F., Stokes, T. M., Sc Leonard, C. M. (1976). Central control of song in the canary. Journal of Comparative Neurology, 165, 457–468
Nottebohm, F., Kasparian, S., & Pandazis, C. (1981). Brain space for a learned task. Brain Research,213, 99–109
Nottebohm, F., Kelley, D. B., & Paton, J. A. (1982). Connections of vocal control nuclei in the canary telencephalon. Journal of Comparative Neurology, 207, 344–357
Okuhata, S., & Saito, N. (1987). Synaptic connections of thalamo-cerebral vocal nuclei of the canary. Brain Research Bulletin, 18, 35–44
Petrinovich, L. (1988). Individual stability, local variability and the cultural transmission of song in white-crowned sparrows (Zonotrichia leucophrys nuttalli). Behavior, 107, 208–240
Petrinovich, L., & Baptista, L. F. (1987). Song development in the white crowned sparrow: Modification of learned song. Animal Behaviour, 35, 961–974
Price, P. (1979). Developmental determinants of structure in zebra finch song. Journal of Comparative and Physiological Psychology, 93, 260–277
Rasika, S., Alvarez-Buylla, A., & Nottebohm, F. (1999). BDNF mediates the effects of testosterone on the survival of new neurons in an adult brain. Neuron, 22, 53–62
Reinke, H., & Wild, J. M. (1998). Identification and connections of inspiratory premotor neurons in songbirds and budgerigar. Journal of Comparative Neurology, 391, 147–163
Ribeiro, S., Cecchi, G. A., Magnasco, M. O., & Mello, C. V. (1998). Toward a song code: Evidence for a syllabic representation in the canary brain. Neuron, 21, 359–371
Riters, L. V., & Ball, G. F. (1999) Lesions to the medial preoptic area affect singing in the male European starling (Sturnus vulgaris). Hormones and Behavior,36, 276–286
Sakaguchi, H., & Yamaguchi, A. (1997). Early song deprivation affects the expression of protein kinase C in the song control nuclei of the zebra finch during a sensitive period of song learning. NeuroReport, S, 2645–2650
Scharff, C., & Nottebohm, E (1991). A comparative study of the behavioral deficits following lesions of various parts of the zebra finch song system-Implications for vocal learning. Journal of Neuroscience, 11, 2896–2913
Scharff, C., Nottebohm, F., & Cynx, J. (1998). Conspecific and heterospecific song discrimination in male zebra finches with lesions in the anterior forebrain pathway. Journal of Neurobiology, 36, 81–90
Schlinger, B. A. (1997). Sex steroids and their actions on the birdsong system. Journal of Neurobiology, 33, 619–631
Schlinger, B. A., & Arnold, A. P. (1991). Androgen effects on the development of the zebra finch song system. Brain Research, 561, 99–105
Schlinger, B. A., & Arnold, A. P. (1992). Plasma sex steroids and tissue aromatization in hatchling zebra fiches: Implications for the sexual differentiation of singing behavior. Endocrinology, 130, 289–299
Schlinger, B. A., & Arnold, A. P. (1991). Androgen effects on the development of the zebra finch song system. Brain Research, 561, 99–105
Schmidt, M. F., & Konishi, M. (1998). Gating of auditory responses in the vocal control system of awake songbirds. Nature Neuroscience, 1, 513–518
Simpson, H. B., & Vicario, D. S. (1991). Early estrogen treatment alone causes female zebra finches to produce learned, male-like vocalizations. Journal of Neurobiology, 22, 755–776
Skaggs, W. E., & McNaughton, B. L. (1996). Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience. Science, 271, 1870–1873
Slater, P. J. B. (1989). Bird song learning: Causes and consequences. Ethology, Ecology and Evolution,1, 19–46. Smith, W. J. (1991). Singing is based on two markedly different kinds of signaling. Journal of Theoretical Biology, 152, 241–253
Sohrabji, E, Nordeen, E. J., & Nordeen, K. W. (1990). Selective impairment of song learning following lesions of a song control nucleus in juvenile zebra finches. Neural Behavioral Biology, 53, 51–63
Solis, M. M., & Doupe, A. J. (1997). Anterior forebrain neurons develop selectivity by an intermediate stage of birdsong learning. Journal of Neuroscience, 17, 6447–6462
Solis, M, M., & Doupe, A. J. (1999). Contributions of tutor and bird’s own song experience to neural selectivity in the songbird anterior forebrain. Journal of Neuroscience, 19, 4559–4584
Soma, K. K., Hartman, V. N., Wingfield, J. C., & Brenowitz, E. A. (1999). Seasonal changes in androgen receptor immunoreactivity in the song nucleus HVc of a wild bird. Journal of Comparative Neurology, 409, 224–236
Spector, D. A. (1992). Wood-warbler song systems. A review of paruline singing behaviors. In D. M. Power (Ed.), Current ornithology (Vol. 9, pp. 199–238). New York: Plenum Press
Staicer, C. A. (1996) Honest advertisement of pairing status: Evidence from a tropical resident wood-warbler. Animal Behaviour, 51, 375–390
Stark, L. L., & Perkel, D.J. (1999). Two-stage, input-specific synaptic maturation in a nucleus essential for vocal production in the zebra finch. Journal of Neuroscience, 20, 9107–9116
Stoddard, P. K. (1996). Vocal recognition of neighbors by territorial passerines. In D. E. Kroodsma & E. H. Miller (Eds.), Ecology and evolution of acoustic communication in birds (pp. 356–374). Ithaca NY: Cornell University Press
Striedter, G. F., Sc Vu, E. T. (1998). Bilateral feedback projections to the forebrain in the premotor network for singing in zebra finches. Journal of Neurobiology, 34, 27–40
Stripling, R., Volman, S. F., & Clayton, D.F. (1997). Response modulation in the zebra finch neostriatum: Relationship to nuclear gene regulation. Journal of Neuroscience, 17, 3883–3893
Suthers, R, A. (1997). Peripheral control and lateralization of birdsong. Journal of Neurobiology, 33, 632–652
Székely, T., Catchpole, C. K., DeVoogd, A., March], Z., Sc DeVoogd, T.J. (1996). Evolutionary changes in a song control area of the brain (HVC) are associated with evolutionary changes in song repertoire among European warblers (Sylviidae). Proceedings of the Royal Society of London,Series B, 263, 607–610
Taber, E. (1964). Intersexuality in birds. In C. N. Armstrong, & J.J. Marshall (Eds.), Intersexuality in vertebrates including man (p. 285). New York: Academic Press
Takahashi, M. M., & Noumura, T. (1987). Sexually dimorphic and laterally asymmetric development of the embryonic duck syrinx: Effect of estrogen on in-vitro cell proliferation and chondrogenesis. Developmental Biology, 121, 417–422
Tchernichovski, O., Schwabl, H., & Nottebohm, F. (1998). Context determines the sex appeal of male zebra finch song. Animal Behaviour, 55, 1003–1010
Theunissen, F. E., & Doupe, A. J. (1998). Temporal and spectral sensitivity of complex auditory neurons in the nucleus HVc of male zebra finches. Journal of Neuroscience, 18, 3786–3802
Titus, R. C. (1998) Short-range and long-range songs: Use of two acoustically distinct song classes by dark-eyed juncos. Auk, 115, 386–393
Todt, D., & Hultsch, H. (1996). Acquisition and performance of song repertoires: Ways of coping with diversity and versatility. In D. E. Kroodsma & E. H. Miller (Eds.), Ecology and evolution of acoustic communication in birds (pp. 79–96). Ithaca, NY: Cornell University Press
Tramontin, A. D., Wingfield, J. C., & Brenowitz, E. A. (1999). Contributions of social cues and photoperiod to seasonal plasticity in the adult avian song control system. Journal of Neuroscience, 19, 476–483
Vallet, E., Kreutzer, M., & Gahr, M. (1996). Testosterone induces sexual release quality in the song of female canaries. Ethology, 102, 617–628
Vates, G. E., Broome, B. M., Mello, C. V., & Nottebohm, F. (1996). Auditory pathways of caudal telencephalon and their relation to the song system of adult male zebra finches (Taenopygia guttata). Journal of Comparative Neurology, 366, 613–642
Vates, G. E., Vicario, D. S., & Nottebohm, E (1997). Reafferent thalamo-“cortical” loops in the song system of oscine songbirds. Journal of Comparative Neurology, 380, 275–290
Vicario, D. S. (1993). A new brainstem pathway for vocal control in the zebra finch song system. Neuroreport, 4, 983–986
Vicario, D. S. (1994). Motor mechanisms relevant to auditory-vocal interactions in songbirds. Brain Behavior and Evolution, 44, 265–278
Vicario, D. S., & Nottebohm, F. (1988). Organization of the zebra finch song control system: I. Representation of syringeal muscles in the hypoglossal nucleus. Journal of Comparative Neurology, 271, 346–354
Volman, S. F., & Khanna, H. (1995). Convergence of untutored song in group-reared zebra finches (Taeniopygia guttata). Journal of Comparative Psychology, 109, 211–221
Vu, E. T., Mazurek, M. E., & Kuo, Y.-C. (1994). Identification of a forebrain motor programming network for the learned song of zebra finches. Journal of Neuroscience, 14, 6924–6934
Vu, E. T., Schmidt, M. F., & Mazurek, M. E. (1998). Interhemispheric coordination of premotor neural activity during singing in adult zebra finches. Journal of Neuroscience, 18, 9088–9098
Wade, J., & Arnold, A. P. (1996). Functional testicular tissue does not masculinize development of the zebra finch song system. Proceedings of the National Academy of Sciences of the USA, 93, 5264–5268
Wade, J., Schlinger, B.A., Hodges, L., & Arnold, A. P. (1994). Fadrozole: A potent and specific inhibitor of aromatase in the zebra finch. General and Comparative Endocrinology, 94, 53–61
Wallhausser, E., & Scheich, H. (1987). Auditory imprinting leads to differential 2 deoxyglucose uptake and dendritic spine loss in the chick rostral forebrain. Developmental Brain Research, 31, 29–44
Wallhhausser-Franke, E., Collins, C. E., & DeVoogd, T.J. (1995). Developmental changes in the distribution of NADPH-diaphorase containing neurons in telencephalic nuclei of the zebra finch song system. Journal of Comparative Neurology, 356, 345–354
Wallhausser-Franke, E., Nixdorf-Bergweiler, B. E., & DeVoogd, T. J. (1995). Song isolation prevents the early loss of spine synapses in song system nucleus 1-MAN of zebra finches. Neurobiology of Learningand Memory, 64, 25–35
Ward, B. C., Nordeen, E. J., & Nordeen, K. W. (1998). Individual variation in neuron number predicts differences in the propensity for avian vocal imitation. Proceedings of the National Academy of Sciences of the USA, 95, 1277–1282
Waser, M. S., & Marler, P. (1977). Song learning in canaries. Journal of Comparative and Physiological Psychology, 91, 1–7
Weichel, K., Schwager, G., Heid, P., Guttinger, H. R., & Pesch, A. (1986). Sex differences in plasma steroid concentrations and singing behaviour during ontogeney in canaries (Serinus canaria). Ethology, 73, 281–294
West, M., & King, A. (1996). Eco-gen-actics: A systems approach to the ontogeny of avian communication. In D. E. Kroodsma & E. H. Miller (Eds.), Ecology and evolution of acoustic communication in birds (pp. 2038). Ithaca, NY: Cornell University Press
West, M. J., Stroud, A. N., & King, A. P. (1983). Mimicry of the human voice by European starlings: The role of social interaction. Wilson Bulletin, 95, 635–640
Whaling, C. S., Solis, M. M., Doupe, A. J., Soha, J. A., & Marler, P. (1997). Acoustic and neural bases for innate recognition of song. Proceedings of Me National Academy of Sciences of the USA, 94, 12694–12698
Wild, J. M. (1997a). Neural pathways for the control of birdsong production. Journal of Neurobiology, 33, 653–670
Wild, J. M. (1997b). Functional anatomy of neural pathways contributing to the control of song production in birds. European Journal of Morphology, 35, 303–325
Wild, J. M. & Williams, M. N. (1999). Rostra] waist of passerine birds: II Intratelencephalic projections to nuclei associated with the auditory and song systems. Journal of Comparative Neurology, 413, 520–525
M. Williams, H. (1990). Models for song learning in the zebra finch: Fathers or others? Animal Behaviour, 39, 745–757
Wingfield, J. C., & Farner, D. S. (1993). Endocrinology of reproduction in wild species. In D. S. Farner, J. R. King, & K. C. Parkes (Eds.), Avian biology (Vol. 9, pp. 163–327). San Diego, CA: Academic Press
Wolff, E. (1959). Endocrine function of the gonad in developing vertebrates. In A. Gorbman (Ed.), Comparative endocrinology (pp. 568–569). New York: Wiley
Yu, A C., & Margoliash, D. (1996). Temporal hierarchical control of singing in birds. Science, 273,18711875
Zann, R. A. (1996). The zebra finch: A synthesis of field and laboratory studies Oxford: Oxford University Press
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DeVoogd, T.J., Lauay, C. (2001). Emerging Psychobiology of the Avian Song System. In: Blass, E.M. (eds) Developmental Psychobiology. Handbook of Behavioral Neurobiology, vol 13. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1209-7_10
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