Abstract
Vocal communication is critical for reproduction and survival across a wide range of species. For vocal communication systems to function, receivers must perform a range of auditory tasks to decode and process acoustic signals. In songbirds, learned vocal signals (songs) can be used by receivers to gain information about the species, sex, identity, and even motivation of the singer. Moreover, young songbirds must hear and memorize songs during development to use them as templates for song learning. This chapter reviews research on the structure and function of the songbird auditory system. In particular, the relationships between the organization, connections, and information-coding properties of the auditory pallium are described and how the functions of those circuits allow birds to perform a range of auditory tasks is considered, including individual recognition, tutor song learning, auditory memory, and mate choice processes.
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References
Adret P (1993) Operant conditioning, song learning and imprinting to taped song in the zebra finch. Anim Behav 46:149–159. https://doi.org/10.1006/anbe.1993.1170
Amin N, Gastpar M, Theunissen FE (2013) Selective and efficient neural coding of communication signals depends on early acoustic and social environment. PLoS One 8:e61417. https://doi.org/10.1371/journal.pone.0061417
Andersson MB (1994) Sexual selection. Princeton University Press
Appeltants D, Del Negro C, Balthazart J (2002) Noradrenergic control of auditory information processing in female canaries. Behav Brain Res 133:221–235. https://doi.org/10.1016/S0166-4328(02)00005-0
Atencio CA, Sharpee TO, Schreiner CE (2009) Hierarchical computation in the canonical auditory cortical circuit. Proc Natl Acad Sci pnas.0908383106. doi: https://doi.org/10.1073/pnas.0908383106
Atoji Y, Wild JM (2009) Afferent and efferent projections of the central caudal nidopallium in the pigeon (Columba livia). J Comp Neurol 517:350–370. https://doi.org/10.1002/cne.22146
Bao S, Chan VT, Merzenich MM (2001) Cortical remodelling induced by activity of ventral tegmental dopamine neurons. Nature 412:79. https://doi.org/10.1038/35083586
Baptista LF, Petrinovich L (1984) Social interaction, sensitive phases and the song template hypothesis in the white-crowned sparrow. Anim Behav 32:172–181. https://doi.org/10.1016/S0003-3472(84)80335-8
Barr HJ, Woolley SC (2018) Developmental auditory exposure shapes responses of catecholaminergic neurons to socially-modulated song. Sci Rep 8:11717. https://doi.org/10.1038/s41598-018-30039-y
Bauer EE, Coleman MJ, Roberts TF, Roy A, Prather JF, Mooney R (2008) A synaptic basis for auditory-vocal integration in the songbird. J Neurosci 28:1509–1522. https://doi.org/10.1523/JNEUROSCI.3838-07.2008
Bee MA, Micheyl C (2008) The cocktail party problem: what is it? How can it be solved? And why should animal behaviorists study it? J Comp Psychol 122:235–251. https://doi.org/10.1037/0735-7036.122.3.235
Beecher MD, Brenowitz EA (2005) Functional aspects of song learning in songbirds. Trends Ecol Evol 20:143–149. https://doi.org/10.1016/j.tree.2005.01.004
Beecher MD, Campbell SE, Burt JM, Hill CE, Nordby JC (2000) Song-type matching between neighbouring song sparrows. Anim Behav 59:21–27. https://doi.org/10.1006/anbe.1999.1276
Beer CG (1971) Individual recognition of voice in the social behavior of birds. In: Lehrman DS, Hinde RA, Shaw E (eds) Advances in the study of behavior. Academic, pp 27–74
Bolhuis JJ, Gahr M (2006) Neural mechanisms of birdsong memory. Nat Rev Neurosci 7:347–357. https://doi.org/10.1038/nrn1904
Braaten RF, Reynolds K (1999) Auditory preference for conspecific song in isolation-reared zebra finches. Anim Behav 58:105–111. https://doi.org/10.1006/anbe.1999.1134
Bradbury JW, Vehrencamp SL (2011) Principles of animal communication. 2nd. Sunderland, Massachusetts: Sinauer
Brainard MS, Doupe AJ (2000) Auditory feedback in learning and maintenance of vocal behaviour. Nat Rev Neurosci 1:31–40. https://doi.org/10.1038/35036205
Bregman AS (1994) Auditory scene analysis: the perceptual Organization of Sound. MIT Press
Brooks RJ, Falls JB (1975) Individual recognition by song in white-throated sparrows. I. Discrimination of songs of neighbors and strangers. Can J Zool 53:879–888. https://doi.org/10.1139/z75-101
Calabrese A, Schumacher JW, Schneider DM, Paninski L, Woolley SMN (2011) A generalized linear model for estimating Spectrotemporal receptive Fields from responses to natural sounds. PLoS One 6:e16104. https://doi.org/10.1371/journal.pone.0016104
Calabrese A, Woolley SMN (2015) Coding principles of the canonical cortical microcircuit in the avian brain. Proc Natl Acad Sci 112:3517–3522. https://doi.org/10.1073/pnas.1408545112
Catchpole CK, Slater PJB (2008) Bird song: biological themes and variations. Cambridge University Press
Chen Y, Clark O, Woolley SC (2017) Courtship song preferences in female zebra finches are shaped by developmental auditory experience. Proc R Soc B Biol Sci 284:20170054. https://doi.org/10.1098/rspb.2017.0054
Chen Y, Matheson LE, Sakata JT (2016) Mechanisms underlying the social enhancement of vocal learning in songbirds. Proc Natl Acad Sci 113:6641–6646. https://doi.org/10.1073/pnas.1522306113
Chew SJ, Mello C, Nottebohm F, Jarvis E, Vicario DS (1995) Decrements in auditory responses to a repeated conspecific song are long-lasting and require two periods of protein synthesis in the songbird forebrain. Proc Natl Acad Sci 92:3406–3410. https://doi.org/10.1073/pnas.92.8.3406
Clayton NS (1990) Subspecies recognition and song learning in zebra finches. Anim Behav 40:1009–1017. https://doi.org/10.1016/S0003-3472(05)80169-1
Clayton NS (1988) Song discrimination learning in zebra finches. Anim Behav 36:1016–1024. https://doi.org/10.1016/S0003-3472(88)80061-7
Dai JB, Chen Y, Sakata JT (2018) EGR-1 expression in catecholamine-synthesizing neurons reflects auditory learning and correlates with responses in auditory processing areas. Neuroscience 379:415–427. https://doi.org/10.1016/j.neuroscience.2018.03.032
David SV, Mesgarani N, Fritz JB, Shamma SA (2009) Rapid synaptic depression explains nonlinear modulation of Spectro-temporal tuning in primary auditory cortex by natural stimuli. J Neurosci 29:3374–3386. https://doi.org/10.1523/JNEUROSCI.5249-08.2009
Dent ML, McClaine EM, Best V, Ozmeral E, Narayan R, Gallun FJ, Sen K, Shinn-Cunningham BG (2009) Spatial unmasking of birdsong in zebra finches (Taeniopygia guttata) and budgerigars (Melopsittacus undulatus). J Comp Psychol 123:357–367. https://doi.org/10.1037/a0016898
Dong S, Clayton DF (2009) Habituation in songbirds. Neurobiol Learn Mem 92:183–188. https://doi.org/10.1016/j.nlm.2008.09.009
Dooling R, Searcy M (1980) Early perceptual selectivity in the swamp sparrow. Dev Psychobiol 13:499–506. https://doi.org/10.1002/dev.420130508
Dugas-Ford J, Rowell JJ, Ragsdale CW (2012) Cell-type homologies and the origins of the neocortex. Proc Natl Acad Sci 109:16974–16979. https://doi.org/10.1073/pnas.1204773109
Dunning JL, Pant S, Bass A, Coburn Z, Prather JF (2014) Mate choice in adult female Bengalese finches: females express consistent preferences for individual males and prefer female-directed song performances. PLoS One 9:e89438. https://doi.org/10.1371/journal.pone.0089438
Elliott TM, Theunissen FE (2011) The avian auditory pallium. In: Winer JA, Schreiner CE (eds) The auditory cortex. Springer US, Boston, MA, pp 429–442
Eriksson D, Wallin L (1986) Male bird song attracts females — a field experiment. Behav Ecol Sociobiol 19:297–299. https://doi.org/10.1007/BF00300645
Fields HL, Hjelmstad GO, Margolis EB, Nicola SM (2007) Ventral tegmental area neurons in learned appetitive behavior and positive reinforcement. Annu Rev Neurosci 30:289–316. https://doi.org/10.1146/annurev.neuro.30.051606.094341
Fisher J (1954) Evolution and bird sociality. Evol Process:71–83
Gentner TQ, Hulse SH, Duffy D, Ball GF (2001) Response biases in auditory forebrain regions of female songbirds following exposure to sexually relevant variation in male song. J Neurobiol 46:48–58. https://doi.org/10.1002/1097-4695(200101)46:1<48::AID-NEU5>3.0.CO;2-3
Gentner TQ, Margoliash D (2003) Neuronal populations and single cells representing learned auditory objects. Nature 424:669–674. https://doi.org/10.1038/nature01731
Gill P, Woolley SMN, Fremouw T, Theunissen FE (2008) What’s that sound? Auditory area CLM encodes stimulus surprise, not intensity or intensity changes. J Neurophysiol 99:2809–2820. https://doi.org/10.1152/jn.01270.2007
Gobes SMH, Bolhuis JJ (2007) Birdsong memory: a neural dissociation between song recognition and production. Curr Biol 17:789–793. https://doi.org/10.1016/j.cub.2007.03.059
Gobes SMH, ter Haar SM, Vignal C, Vergne AL, Mathevon N, Bolhuis JJ (2009) Differential responsiveness in brain and behavior to sexually dimorphic long calls in male and female zebra finches. J Comp Neurol 516:312–320. https://doi.org/10.1002/cne.22113
Gobes SMH, Zandbergen MA, Bolhuis JJ (2010) Memory in the making: localized brain activation related to song learning in young songbirds. Proc R Soc Lond B Biol Sci 277:3343–3351. https://doi.org/10.1098/rspb.2010.0870
Graham DJ, Field DJ (2007) Efficient coding of natural images. New Encyclopedia of Neuroscience 1
Hansen BJ, Chelaru MI, Dragoi V (2012) Correlated variability in laminar cortical circuits. Neuron 76:590–602. https://doi.org/10.1016/j.neuron.2012.08.029
Harris KD, Mrsic-Flogel TD (2013) Cortical connectivity and sensory coding. Nature 503:51–58. https://doi.org/10.1038/nature12654
Hauber ME, Woolley SMN, Cassey P, Theunissen FE (2013) Experience dependence of neural responses to different classes of male songs in the primary auditory forebrain of female songbirds. Behav Brain Res 243:184–190. https://doi.org/10.1016/j.bbr.2013.01.007
Heil P, Scheich H (1991) Functional organization of the avian auditory cortex analogue. I. Topographic representation of isointensity bandwidth. Brain Res 539:110–120. https://doi.org/10.1016/0006-8993(91)90692-O
Hernandez AM, MacDougall-Shackleton SA (2004) Effects of early song experience on song preferences and song control and auditory brain regions in female house finches (Carpodacus mexicanus). J Neurobiol 59:247–258. https://doi.org/10.1002/neu.10312
Horita H, Kobayashi M, Liu W, Oka K, Jarvis ED, Wada K (2012) Specialized motor-driven dusp1 expression in the song Systems of Multiple Lineages of vocal learning birds. PLoS One 7:e42173. https://doi.org/10.1371/journal.pone.0042173
Horita H, Wada K, Rivas M, Hara E, Jarvis ED (2010) The dusp1 immediate early gene is regulated by natural stimuli predominantly in sensory input neurons. J Comp Neurol NA-NA:NA. https://doi.org/10.1002/cne.22370
Hose B, Langner G, Scheich H (1987) Topographic representation of periodicities in the forebrain of the mynah bird: one map for pitch and rhythm? Brain Res 422:367–373. https://doi.org/10.1016/0006-8993(87)90946-2
Ikeda MZ, Jeon SD, Cowell RA, Remage-Healey L (2015) Norepinephrine modulates coding of complex vocalizations in the songbird auditory cortex independent of local Neuroestrogen synthesis. J Neurosci 35:9356–9368. https://doi.org/10.1523/JNEUROSCI.4445-14.2015
Immelmann K (1969) Song development in the zebra finch and other estrildid finches. Bird Vocalizations:61–77
Jeanne JM, Thompson JV, Sharpee TO, Gentner TQ (2011) Emergence of learned categorical representations within an auditory forebrain circuit. J Neurosci 31:2595–2606. https://doi.org/10.1523/JNEUROSCI.3930-10.2011
Kao MH, Brainard MS (2006) Lesions of an avian basal ganglia circuit prevent context-dependent changes to song variability. J Neurophysiol 96:1441–1455. https://doi.org/10.1152/jn.01138.2005
Karten HJ (1969) The Organization of the Avian telencephalon and some speculations on the phylogeny of the Amniote telencephalon∗. Ann N Y Acad Sci 167:164–179. https://doi.org/10.1111/j.1749-6632.1969.tb20442.x
Karten HJ (2013) Neocortical evolution: neuronal circuits Arise independently of lamination. Curr Biol 23:R12–R15. https://doi.org/10.1016/j.cub.2012.11.013
Kim G, Doupe A (2011) Organized representation of Spectrotemporal features in songbird auditory forebrain. J Neurosci 31:16977–16990. https://doi.org/10.1523/JNEUROSCI.2003-11.2011
Konishi M (2004) The role of auditory feedback in birdsong. Ann N Y Acad Sci 1016:463–475. https://doi.org/10.1196/annals.1298.010
Kruse A (2004) Context-specific habituation of the zenk gene response to song in adult zebra finches. Neurobiol Learn Mem 82:99–108. https://doi.org/10.1016/j.nlm.2004.05.001
Kruse AA, Stripling R, Clayton DF (2000) Minimal experience required for immediate-early gene induction in Zebra finch Neostriatum. Neurobiol Learn Mem 74:179–184. https://doi.org/10.1006/nlme.2000.3968
Lampen J, Jones K, McAuley JD, Chang S-E, Wade J (2014) Arrhythmic song exposure increases ZENK expression in auditory cortical areas and nucleus Taeniae of the adult Zebra finch. PLoS One 9:e108841. https://doi.org/10.1371/journal.pone.0108841
Lauay C, Gerlach NM, Adkins-Regan E, DeVoogd TJ (2004) Female zebra finches require early song exposure to prefer high-quality song as adults. Anim Behav 68:1249–1255. https://doi.org/10.1016/j.anbehav.2003.12.025
Leitner S, Voigt C, Metzdorf R, Catchpole CK (2005) Immediate early gene (ZENK, arc) expression in the auditory forebrain of female canaries varies in response to male song quality. J Neurobiol 64:275–284. https://doi.org/10.1002/neu.20135
London SE, Clayton DF (2008) Functional identification of sensory mechanisms required for developmental song learning. Nat Neurosci 11:579–586. https://doi.org/10.1038/nn.2103
Lu K, Vicario DS (2017) Familiar but unexpected: effects of sound context statistics on auditory responses in the songbird forebrain. J Neurosci 37:12006–12017. https://doi.org/10.1523/JNEUROSCI.5722-12.2017
Lynch KS, Ball GF (2008) Noradrenergic deficits Alter processing of communication signals in female songbirds. Brain Behav Evol 72:207–214. https://doi.org/10.1159/000157357
Machens CK, Wehr MS, Zador AM (2004) Linearity of cortical receptive Fields measured with natural sounds. J Neurosci 24:1089–1100. https://doi.org/10.1523/JNEUROSCI.4445-03.2004
Mandelblat-Cerf Y, Las L, Denisenko N, Fee MS (2014) A role for descending auditory cortical projections in songbird vocal learning. eLife. https://elifesciences.org/articles/02152.
Marler P (1970) A comparative approach to vocal learning: song development in white-crowned sparrows. J Comp Physiol Psychol 71:1–25. https://doi.org/10.1037/h0029144
Marler P, Peters S (1977) Selective vocal learning in a sparrow. Science 198:519–521. https://doi.org/10.1126/science.198.4316.519
Marler P, Peters S (1981) Sparrows learn adult song and more from memory. Science 213:780–782. https://doi.org/10.1126/science.213.4509.780
Martins ARO, Froemke RC (2015) Coordinated forms of noradrenergic plasticity in the locus coeruleus and primary auditory cortex. Nat Neurosci, 18:1483. https://doi.org/10.1038/nn.4090
Meliza CD, Margoliash D (2012) Emergence of selectivity and tolerance in the avian auditory cortex. J Neurosci 32:15158–15168. https://doi.org/10.1523/JNEUROSCI.0845-12.2012
Mello C, Nottebohm F, Clayton D (1995) Repeated exposure to one song leads to a rapid and persistent decline in an immediate early gene’s response to that song in zebra finch telencephalon. J Neurosci 15:6919–6925. https://doi.org/10.1523/JNEUROSCI.15-10-06919.1995
Miller DB (1979a) The acoustic basis of mate recognition by female zebra finches. Anim Behav 27:376–380
Miller DB (1979b) Long-term recognition of father’s song by female zebra finches. Nature 280:389–391. https://doi.org/10.1038/280389a0
Moore RC, Lee T, Theunissen FE (2013) Noise-invariant neurons in the avian auditory cortex: hearing the song in noise. PLoS Comput Biol 9:e1002942. https://doi.org/10.1371/journal.pcbi.1002942
Moore JM, Woolley SM (2019) Emergent tuning for learned vocalizations in auditory cortex. Nat Neurosci 22:1469–76. https://doi.org/10.1038/s41593-019-0458-4
Moseley LJ (1979) Individual auditory recognition in the least tern (Sterna albifrons). Auk Ornithol Adv 96:31–39. https://doi.org/10.1093/auk/96.1.31
Müller CM, Leppelsack H-J (1985) Feature extraction and tonotopic organization in the avian auditory forebrain. Exp Brain Res 59:587–599. https://doi.org/10.1007/BF00261351
Müller SC, Scheich H (1985) Functional organization of the avian auditory field L. J Comp Physiol A 156:1–12. https://doi.org/10.1007/BF00610661
Nagel K, Kim G, McLendon H, Doupe A (2011) A bird brain’s view of auditory processing and perception. Hear Res 273:123–133. https://doi.org/10.1016/j.heares.2010.08.008
Nagel KI, Doupe AJ (2008) Organizing principles of spectro-temporal encoding in the avian primary auditory area Field L. Neuron 58:938–955. https://doi.org/10.1016/j.neuron.2008.04.028
Nelson DA (2000) A preference for own-subspecies’ song guides vocal learning in a song bird. Proc Natl Acad Sci 97:13348–13353. https://doi.org/10.1073/pnas.240457797
Nelson DA, Marler P (1993) Innate recognition of song in white-crowned sparrows: a role in selective vocal learning? Anim Behav 46:806–808. https://doi.org/10.1006/anbe.1993.1258
Nordeen KW, Nordeen EJ (1992) Auditory feedback is necessary for the maintenance of stereotyped song in adult zebra finches. Behav Neural Biol 57:58–66. https://doi.org/10.1016/0163-1047(92)90757-U
Okanoya K, Dooling RJ (1987) Hearing in passerine and psittacine birds: a comparative study of absolute and masked auditory thresholds. J Comp Psychol 101:7–15. https://doi.org/10.1037/0735-7036.101.1.7
Petrinovich L, Baptista LF (1987) Song development in the white-crowned sparrow: modification of learned song. Anim Behav 35:961–974. https://doi.org/10.1016/S0003-3472(87)80153-7
Phan ML, Pytte CL, Vicario DS (2006) Early auditory experience generates long-lasting memories that may subserve vocal learning in songbirds. Proc Natl Acad Sci 103:1088–1093. https://doi.org/10.1073/pnas.0510136103
Ribeiro S, Cecchi GA, Magnasco MO, Mello CV (1998) Toward a song code: evidence for a syllabic representation in the canary brain. Neuron 21:359–371. https://doi.org/10.1016/S0896-6273(00)80545-0
Richner H (2016) Interval singing links to phenotypic quality in a songbird. Proc Natl Acad Sci 113:12763–12767. https://doi.org/10.1073/pnas.1610062113
Riebel K (2009) Chapter 6 song and female mate choice in Zebra finches: a review. In: Advances in the study of behavior. Academic, pp 197–238. https://doi.org/10.1016/S0065-3454(09)40006-8
Robertson BC (1996) Vocal mate recognition in a monogamous, flock-forming bird, the silvereye, Zosterops lateralis. Anim Behav 51:303–311. https://doi.org/10.1006/anbe.1996.0030
Sakata JT, Vehrencamp SL (2012) Integrating perspectives on vocal performance and consistency. J Exp Biol 215:201–209. https://doi.org/10.1242/jeb.056911
Sara SJ, Bouret S (2012) Orienting and reorienting: the locus Coeruleus mediates cognition through arousal. Neuron 76:130–141. https://doi.org/10.1016/j.neuron.2012.09.011
Schneider DM, Woolley SMN (2013) Sparse and background-invariant coding of vocalizations in auditory scenes. Neuron 79:141–152. https://doi.org/10.1016/j.neuron.2013.04.038
Schubloom HE, Woolley SC (2016) Variation in social relationships relates to song preferences and EGR1 expression in a female songbird. Dev Neurobiol 76:1029–1040. https://doi.org/10.1002/dneu.22373
Searcy WA, Brenowitz EA (1988) Sexual differences in species recognition of avian song. Nature 332:152–154. https://doi.org/10.1038/332152a0
Sen K, Theunissen FE, Doupe AJ (2001) Feature analysis of natural sounds in the songbird auditory forebrain. J Neurophysiol 86:1445–1458. https://doi.org/10.1152/jn.2001.86.3.1445
Sossinka R, Böhner J (1980) Song types in the zebra finch poephila guttata castanotis1. Z Für Tierpsychol 53:123–132. https://doi.org/10.1111/j.1439-0310.1980.tb01044.x
Striedter GF (1997) The telencephalon of tetrapods in evolution; pp. 205–213. Brain Behav Evol 49:205–213. https://doi.org/10.1159/000112992
Stripling R, Milewski L, Kruse AA, Clayton DF (2003) Rapidly learned song-discrimination without behavioral reinforcement in adult male zebra finches (Taeniopygia guttata). Neurobiol Learn Mem 79:41–50. https://doi.org/10.1016/S1074-7427(02)00005-9
Temeles EJ (1994) The role of neighbours in territorial systems: when are they “dear enemies”. Anim Behav 47:339–350. https://doi.org/10.1006/anbe.1994.1047
Terleph TA, Lu K, Vicario DS (2008) Response properties of the auditory telencephalon in songbirds change with recent experience and season. PLoS One 3:e2854. https://doi.org/10.1371/journal.pone.0002854
Terpstra NJ, Bolhuis JJ, Riebel K, van der BJMM, den B-VAM (2006) Localized brain activation specific to auditory memory in a female songbird. J Comp Neurol 494:784–791. https://doi.org/10.1002/cne.20831
Theunissen FE, Amin N, Shaevitz SS, Woolley SMN, Fremouw T, Hauber ME (2004) Song selectivity in the song system and in the auditory forebrain. Ann N Y Acad Sci 1016:222–245. https://doi.org/10.1196/annals.1298.023
Theunissen FE, Doupe AJ (1998) Temporal and spectral sensitivity of complex auditory neurons in the nucleus HVc of male zebra finches. J Neurosci 18:3786–3802. https://doi.org/10.1523/JNEUROSCI.18-10-03786.1998
Theunissen FE, Sen K, Doupe AJ (2000) Spectral-temporal receptive fields of nonlinear auditory neurons obtained using natural sounds. J Neurosci 20:2315–2331. https://doi.org/10.1523/JNEUROSCI.20-06-02315.2000
Tibbetts EA, Dale J (2007) Individual recognition: it is good to be different. Trends Ecol Evol 22:529–537. https://doi.org/10.1016/j.tree.2007.09.001
Vallet E, Beme I, Kreutzer M (1998) Two-note syllables in canary songs elicit high levels of sexual display. Anim Behav 55:291–297. https://doi.org/10.1006/anbe.1997.0631
Vallet E, Kreutzer M (1995) Female canaries are sexually responsive to special song phrases. Anim Behav 49:1603–1610. https://doi.org/10.1016/0003-3472(95)90082-9
Van Ruijssevelt L, Chen Y, von Eugen K, Hamaide J, De Groof G, Verhoye M, Güntürkün O, Woolley SC, Van der Linden A (2018) fMRI reveals a novel region for evaluating acoustic information for mate choice in a female songbird. Curr Biol 28:711–721.e6. https://doi.org/10.1016/j.cub.2018.01.048
Vates GE, Broome BM, Mello CV, Nottebohm F (1996) Auditory pathways of caudal telencephalon and their relation to the song system of adult male zebra finches (Taenopygia guttata). J Comp Neurol 366:613–642. https://doi.org/10.1002/(SICI)1096-9861(19960318)366:4<613::AID-CNE5>3.0.CO;2-7
Velho TAF, Lu K, Ribeiro S, Pinaud R, Vicario D, Mello CV (2012) Noradrenergic control of gene expression and long-term neuronal adaptation evoked by learned vocalizations in songbirds. PLoS One 7:e36276. https://doi.org/10.1371/journal.pone.0036276
Wang Y, Brzozowska-Prechtl A, Karten HJ (2010) Laminar and columnar auditory cortex in avian brain. Proc Natl Acad Sci 107:12676–12681. https://doi.org/10.1073/pnas.1006645107
White SJ (1971) Selective responsiveness by the gannet (Sula bassana) to played-back class. Anim Behav 19:125–131. https://doi.org/10.1016/S0003-3472(71)80146-X
Woolley SC, Doupe AJ (2008) Social context–induced song variation affects female behavior and gene expression. PLoS Biol 6:e62. https://doi.org/10.1371/journal.pbio.0060062
Woolley SMN (2012) Early experience shapes vocal neural coding and perception in songbirds. Dev Psychobiol 54:612–631. https://doi.org/10.1002/dev.21014
Woolley SMN (2008) Auditory feedback and singing in adult birds. In: Zeigler HP, Marler P (eds) Neuroscience of birdsong. Cambridge University Press, Cambridge, pp 228–239
Woolley SMN, Moore JM (2011) Coevolution in communication senders and receivers: vocal behavior and auditory processing in multiple songbird species. Ann N Y Acad Sci 1225:155–165. https://doi.org/10.1111/j.1749-6632.2011.05989.x
Woolley SMN, Rubel EW (1997) Bengalese finches Lonchura Striata domestica depend upon auditory feedback for the maintenance of adult song. J Neurosci 17:6380–6390. https://doi.org/10.1523/JNEUROSCI.17-16-06380.1997
Woolley SMN, Rubel EW (1999) High-frequency auditory feedback is not required for adult song maintenance in bengalese finches. J Neurosci 19:358–371. https://doi.org/10.1523/JNEUROSCI.19-01-00358.1999
Woolley SMN, Fremouw TE, Hsu A, Theunissen FE (2005) Tuning for spectro-temporal modulations as a mechanism for auditory discrimination of natural sounds. Nat Neurosci 8:1371–1379. https://doi.org/10.1038/nn1536
Woolley SMN, Gill PR, Fremouw T, Theunissen FE (2009) Functional groups in the avian auditory system. J Neurosci 29:2780–2793. https://doi.org/10.1523/JNEUROSCI.2042-08.2009
Woolley SMN, Hauber ME, Theunissen FE (2010) Developmental experience alters information coding in auditory midbrain and forebrain neurons. Dev Neurobiol 70:235–252. https://doi.org/10.1002/dneu.20783
Yanagihara S, Yazaki-Sugiyama Y (2016) Auditory experience-dependent cortical circuit shaping for memory formation in bird song learning. Nat Commun 7:11946. https://doi.org/10.1038/ncomms11946
Yang LM, Vicario DS (2015) Exposure to a novel stimulus environment alters patterns of lateralization in avian auditory cortex. Neuroscience 285:107–118. https://doi.org/10.1016/j.neuroscience.2014.10.022
Ydenberg RC, Giraldeau LA, Falls JB (1988) Neighbours, strangers, and the asymmetric war of attrition. Anim Behav 36:343–347. https://doi.org/10.1016/S0003-3472(88)80004-6
Zann RA (1996) The Zebra finch: a synthesis of Field and laboratory studies. Oxford University Press
Zaretsky MD, Konishi M (1976) Tonotopic organization in the avian telencephalon. Brain Res 111:167–171. https://doi.org/10.1016/0006-8993(76)91058-1
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Sarah C. Woolley declares that she has no conflict of interest. Sarah M. N. Woolley declares that she has no conflict of interest.
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Woolley, S.C., Woolley, S.M.N. (2020). Integrating Form and Function in the Songbird Auditory Forebrain. In: Sakata, J., Woolley, S., Fay, R., Popper, A. (eds) The Neuroethology of Birdsong. Springer Handbook of Auditory Research, vol 71. Springer, Cham. https://doi.org/10.1007/978-3-030-34683-6_5
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