Parallel pathways and convergence onto HVc and adjacent neostriatum of adult zebra finches (Taeniopygia guttata)

The structure and connectivity of the forebrain nucleus HVc, a site of sensorimotor integration in the song control system of oscine birds, were investigated in adult zebra finches. HVc in males comprises three cytoarchitectonic subdivisions: the commonly recognized central region with large and medium‐sized darkly staining cells, a ventral caudomedial region with densely packed small and medium‐sized cells, and a dorsolateral region with oblong cells and rows of cells. All three subdivisions project to area X and the robust nucleus of the archistriatum, with more complexity in the classes and distribution of cells than previously reported. In females, HVc is very small and has a cytoarchitecture distinct from that of the three male subdivisions. The structure of HVc in females treated with estradiol at 15 days of age is similar to male HVc.

[1]  H. Karten,et al.  The organization of the ascending auditory pathway in the pigeon (Columba livia). I. Diencephalic projections of the inferior colliculus (nucleus mesencephali lateralis, pars dorsalis). , 1967, Brain research.

[2]  H. Karten,et al.  The ascending auditory pathway in the pigeon (Columba livia). II. Telencephalic projections of the nucleus ovoidalis thalami. , 1968, Brain research.

[3]  A. Arnold,et al.  Hormone concentrating cells in vocal control and other areas of the brain of the zebra finch (Poephila guttata) , 1976, The Journal of comparative neurology.

[4]  F. Nottebohm,et al.  Central control of song in the canary, Serinus canarius , 1976, The Journal of comparative neurology.

[5]  F. Nottebohm,et al.  Projections of a telencephalic auditory nucleus– field L–in the canary , 1979, The Journal of comparative neurology.

[6]  F. Nottebohm,et al.  Brain space for a learned task , 1981, Brain Research.

[7]  L. C. Katz,et al.  Auditory responses in the zebra finch's motor system for song , 1981, Brain Research.

[8]  H. Leppelsack,et al.  Cell types of the auditory caudomedial neostriatum of the starling (Sturnus vulgaris) , 1981, The Journal of comparative neurology.

[9]  F. Nottebohm A brain for all seasons: cyclical anatomical changes in song control nuclei of the canary brain. , 1981, Science.

[10]  M. Gurney,et al.  Hormonal control of cell form and number in the zebra finch song system , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  F. Nottebohm,et al.  Connections of vocal control nuclei in the canary telencephalon , 1982, The Journal of comparative neurology.

[12]  H. Nauta Tracing neural connections with horseradish peroxidase M. M. Mesulam (Ed.). John Wiley, Chichester (1982). 280 pp., Cloth, $52.00/£22.00; paper, $26.00/£11.00 , 1982, Neuroscience.

[13]  D. Margoliash Acoustic parameters underlying the responses of song-specific neurons in the white-crowned sparrow , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  F. Nottebohm,et al.  Neuronal production, migration, and differentiation in a vocal control nucleus of the adult female canary brain. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[15]  F. Nottebohm,et al.  Population differences in complexity of a learned skill are correlated with the brain space involved. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[16]  D Margoliash,et al.  Auditory representation of autogenous song in the song system of white-crowned sparrows. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Arnold,et al.  Ontogeny of brain nuclei controlling song learning and behavior in zebra finches , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  D Margoliash,et al.  Preference for autogenous song by auditory neurons in a song system nucleus of the white-crowned sparrow , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  F. Nottebohm,et al.  Developmental and seasonal changes in canary song and their relation to changes in the anatomy of song-control nuclei. , 1986, Behavioral and neural biology.

[20]  Paul D. Gamlin,et al.  A second ascending visual pathway from the optic tectum to the telencephalon in the pigeon (Columba livia) , 1986, The Journal of comparative neurology.

[21]  Eliot A. Brenowitz,et al.  Interspecific comparisons of the size of neural song control regions and song complexity in duetting birds: evolutionary implications , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  S. Brauth,et al.  Auditory Pathways in the Budgerigar , 1987 .

[23]  E. Nordeen,et al.  Estrogen accumulation in zebra finch song control nuclei: implications for sexual differentiation and adult activation of song behavior. , 1987, Journal of neurobiology.

[24]  Auditory pathways in the budgerigar. II. Intratelencephalic pathways. , 1988, Brain, behavior and evolution.

[25]  P. Whiting,et al.  Autoradiographic localization of nicotinic acetylcholine receptors in the brain of the zebra finch (Poephila guttata) , 1988, The Journal of comparative neurology.

[26]  Sandra A. Brown,et al.  Axonal connections of a forebrain nucleus involved with vocal learning in zebra finches , 1989, The Journal of comparative neurology.

[27]  R. Clower,et al.  Song-related brain regions in the red-winged blackbird are affected by sex and season but not repertoire size. , 1989, Journal of neurobiology.

[28]  B. Nixdorf,et al.  Morphology of Golgi‐impregnated neurons in hyperstriatum ventralis, pars caudalis in adult male and female canaries , 1989, The Journal of comparative neurology.

[29]  O. Güntürkün,et al.  Sensory properties and afferents of the N. dorsolateralis posterior thalami of the pigeon , 1990, The Journal of comparative neurology.

[30]  H. Williams,et al.  Song learning in birds: the relation between perception and production. , 1990, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[31]  F. Nottebohm,et al.  Birth of projection neurons in adult avian brain may be related to perceptual or motor learning. , 1990, Science.

[32]  M. Gahr,et al.  Delineation of a brain nucleus: Comparisons of cytochemical, hodological, and cytoarchitectural views of the song control nucleus HVC of the adult canary , 1990, The Journal of comparative neurology.

[33]  Eliot A. Brenowitz Evolution of the vocal control system in the avian brain , 1991 .

[34]  H. Scheich,et al.  Parvalbumin and calbindin-D28K immunoreactivity as developmental markers of auditory and vocal motor nuclei of the zebra finch , 1991, Neuroscience.

[35]  H. Scheich,et al.  Functional organization of the avian auditory cortex analogue. I. Topographic representation of isointensity bandwidth , 1991, Brain Research.

[36]  F. Nottebohm,et al.  Production and survival of projection neurons in a forebrain vocal center of adult male canaries , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  A. Doupe,et al.  Song-selective auditory circuits in the vocal control system of the zebra finch. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[38]  A. Arnold,et al.  The development of afferent projections to the robust archistriatal nucleus in male zebra finches: a quantitative electron microscopic study , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[39]  D. Margoliash,et al.  Cytoarchitectonic organization and morphology of cells of the field L complex in male zebra finches (taenopygia guttata) , 1992, The Journal of comparative neurology.

[40]  D. Margoliash,et al.  Temporal and harmonic combination-sensitive neurons in the zebra finch's HVc , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  J. Tepper,et al.  The shell region of the nucleus ovoidalis: A subdivision of the avian auditory thalamus , 1992, The Journal of comparative neurology.

[42]  F. Nottebohm,et al.  High vocal center growth and its relation to neurogenesis, neuronal replacement and song acquisition in juvenile canaries. , 1992, Journal of neurobiology.

[43]  H. Karten,et al.  Connections of the auditory forebrain in the pigeon (columba livia) , 1993, The Journal of comparative neurology.

[44]  S. Volman,et al.  Development of neural selectivity for birdsong during vocal learning , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  D. Vicario,et al.  Song-selective auditory input to a forebrain vocal control nucleus in the zebra finch. , 1993, Journal of neurobiology.

[46]  Gregory F Ball,et al.  Sexual dimorphism in the volume of song control nuclei in European starlings: Assessment by a Nissl stain and autoradiography for muscarinic cholinergic receptors , 1993, The Journal of comparative neurology.

[47]  S. Healy,et al.  Relations between song repertoire size and the volume of brain nuclei related to song: comparative evolutionary analyses amongst oscine birds , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[48]  S. Bottjer,et al.  Hormone-induced changes in identified cell populations of the higher vocal center in male canaries. , 1993, Journal of neurobiology.

[49]  D Margoliash,et al.  Distributed representation in the song system of oscines: evolutionary implications and functional consequences. , 1994, Brain, behavior and evolution.

[50]  D Margoliash,et al.  Global synchronous response to autogenous song in zebra finch HVc. , 1994, Journal of neurophysiology.

[51]  E.C.L. Vu,et al.  Identification of a forebrain motor programming network for the learned song of zebra finches , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.