1990
DOI: 10.1523/jneurosci.10-05-01541.1990
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Brain pathways for learned and unlearned vocalizations differ in zebra finches

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Cited by 357 publications
(340 citation statements)
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“…This conclusion is also supported by the previous deafening and syringeal denervation results, which have been obtained from zebra finches as well (Price, 1979;Simpson and Vicario, 1990;Nordeen and Nordeen, 1992). Electrical stimulation of RA probably perturbed motor performance more pervasively than syringeal denervation because the neural control signals from RA are distributed to multiple effector systems involved in singing (Vicario, 199 1;Wild, 1993Wild, , 1994.…”
Section: Discussionsupporting
confidence: 67%
“…This conclusion is also supported by the previous deafening and syringeal denervation results, which have been obtained from zebra finches as well (Price, 1979;Simpson and Vicario, 1990;Nordeen and Nordeen, 1992). Electrical stimulation of RA probably perturbed motor performance more pervasively than syringeal denervation because the neural control signals from RA are distributed to multiple effector systems involved in singing (Vicario, 199 1;Wild, 1993Wild, , 1994.…”
Section: Discussionsupporting
confidence: 67%
“…1b). These behavioural and neuroanatomical traits have not been found in non-vocal-learners 6 , which develop species-specific vocalizations in the absence of hearing 7 , and have no known forebrain vocalmotor control 8,9 . In non-vocal-learners, the vocal pathway is thought to consist solely of midbrain and brainstem nuclei [9][10][11] .…”
mentioning
confidence: 85%
“…L ong calls and song were recorded and used as the behavioral data. Both kinds of vocalization are learned (Immelmann, 1969;Price, 1979;Z ann, 1985) and controlled by the forebrain motor pathways for production of learned sounds (Simpson and Vicario, 1990).…”
Section: Methodsmentioning
confidence: 99%