Birth of projection neurons in adult avian brain may be related to perceptual or motor learning.

Projection neurons that form part of the motor pathway for song control continue to be produced and to replace older projection neurons in adult canaries and zebra finches. This is shown by combining [3H]thymidine, a cell birth marker, and fluorogold, a retrogradely transported tracer of neuronal connectivity. Species and seasonal comparisons suggest that this process is related to the acquisition of perceptual or motor memories. The ability of an adult brain to produce and replace projection neurons should influence our thinking on brain repair.

[1]  Fernando Nottebohm,et al.  Migration of young neurons in adult avian brain , 1988, Nature.

[2]  F. Nottebohm Birdsong as a Model in Which to Study Brain Processes Related to Learning , 1984 .

[3]  A. Arnold,et al.  Changes in neuronal number, density and size account for increases in volume of song-control nuclei during song development in zebra finches , 1986, Neuroscience Letters.

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

[5]  L. A. Eales Song learning in zebra finches: some effects of song model availability on what is learnt and when , 1985, Animal Behaviour.

[6]  F. Nottebohm,et al.  Neurons generated in the adult brain are recruited into functional circuits. , 1984, Science.

[7]  Joseph Altman,et al.  Directions in neurogenetic gradients and patterns of anatomical connections in the telencephalon , 1987, Progress in Neurobiology.

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

[9]  E. Nordeen,et al.  Neurogenesis and sensitive periods in avian song learning , 1990, Trends in Neurosciences.

[10]  F. Nottebohm,et al.  Birth of projection neurons in the higher vocal center of the canary forebrain before, during, and after song learning. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

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

[12]  P. Marler,et al.  Addition of song-related neurons in swamp sparrows coincides with memorization, not production, of learned songs. , 1989, Journal of neurobiology.

[13]  D. Vicario,et al.  Brain pathways for learned and unlearned vocalizations differ in zebra finches , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  H. Williams,et al.  Auditory responses in avian vocal motor neurons: a motor theory for song perception in birds. , 1985, Science.

[15]  F. Nottebohm Neuronal Replacement in Adulthood , 1985, Annals of the New York Academy of Sciences.

[16]  A. Burkhalter,et al.  Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex , 1984, Nature.

[17]  L. C. Katz,et al.  Green fluorescent latex microspheres: A new retrograde tracer , 1990, Neuroscience.

[18]  Arturo Alvarez-Buylla,et al.  Simple microcomputer system for mapping tissue sections with the light microscope , 1988, Journal of Neuroscience Methods.

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

[21]  Masakazu Konishi,et al.  Neuronal growth, atrophy and death in a sexually dimorphic song nucleus in the zebra finch brain , 1985, Nature.

[22]  E. Nordeen,et al.  Projection neurons within a vocal motor pathway are born during song learning in zebra finches , 1988, Nature.