1995
DOI: 10.1016/0361-9230(94)00202-c
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Distribution of dopaminergic fibers and neurons in visual and auditory cortices of the harbor porpoise and pilot whale

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Cited by 30 publications
(31 citation statements)
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“…This is particularly true of the primary visual cortex, where humans and other primates exhibit TH-ir axons only in layer I and DAergic axons are rarely found in rodent visual cortex (Gaspar et al, 1989;Berger et al, 1991). In contrast, the cetacean primary visual cortex is innervated throughout all layers, and it is more densely innervated than the auditory cortex, whereas the reverse is true for the other mammals (Hof et al, 1995). Such phylogenetic differences strongly suggest a potential role for this neurotransmitter in brain evolution.…”
Section: Discussionmentioning
confidence: 99%
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“…This is particularly true of the primary visual cortex, where humans and other primates exhibit TH-ir axons only in layer I and DAergic axons are rarely found in rodent visual cortex (Gaspar et al, 1989;Berger et al, 1991). In contrast, the cetacean primary visual cortex is innervated throughout all layers, and it is more densely innervated than the auditory cortex, whereas the reverse is true for the other mammals (Hof et al, 1995). Such phylogenetic differences strongly suggest a potential role for this neurotransmitter in brain evolution.…”
Section: Discussionmentioning
confidence: 99%
“…A broader view of phylogenetic differences has been provided by Hof and collaborators in an analysis of cortical TH-ir axon distribution in the harbor porpoise and pilot whale (Hof et al, 1995). Their findings revealed a different pattern of innervation of auditory and visual cortices of cetaceans compared to that of other mammals.…”
Section: Discussionmentioning
confidence: 99%
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“…As there is a 55-60 million year divergence between cetaceans and the phylogenetically closest group (the artiodactyls), odontocete brains represent a blend of early mammalian and uniquely derived features (Ridgway, 1986;Glezer et al, 1988;Ridgway, 1990;Manger et al, 1998). The differences between cetacean and other mammalian brains of similar size have been noted at the level of cortical cytoarchitecture and histochemistry (Garey et al, 1985;Garey and Leuba, 1986;Glezer et al, , 1992aGlezer et al, , b, 1993Glezer et al, , 1998Hof et al, 1992Hof et al, , 1995, cortical surface configuration (Jacobs et al, 1979;Morgane et al, 1980;Haug, 1987), and subcortical structural morphology (Tarpley and Ridgway, 1994;Glezer et al, 1995a, b). These differences are also manifest during ontogeny (Oelschlager and Buhl, 1985;Buhl and Oelschlager, 1988;Oelschlager and Kemp, 1998).…”
mentioning
confidence: 99%
“…Because of the 55-to 60-million year divergence between cetaceans and other mammals, odontocete brains represent a blend of early mammalian features and uniquely derived characteristics (Glezer et al, 1988;Manger et al, 1998;Ridgway, 1986Ridgway, , 1990. The differences between dolphin and other mammalian brains of similar size have been noted at the level of cortical cytoarchitecture and immunohistochemistry (Garey et al, 1985;Garey and Leuba, 1986;Glezer et al, , 1992aGlezer et al, ,b, 1993Glezer et al, , 1998Hof et al, 1992Hof et al, , 1995, cortical surface morphology (Haug, 1987;Jacobs et al, 1979;Morgane et al, 1980) and subcortical structures (Glezer et al, 1995a,b;Tarpley and Ridgway, 1994). These differences are also manifest during ontogenesis (Buhl and Oelschlager, 1988;Oelschlager and Buhl, 1985;Oelschlager and Kemp, 1998).…”
mentioning
confidence: 99%