Comparative Vertebrate Neuroanatomy: Evolution and Adaptation
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The pallial area considered homologous to the hippocampus in teleost fish is the dorsolateral telencephalic region.
“Taking into account the process of telencephalic eversion in teleost fish and the fact that the hippocampus originates from the most distal region of the embryonic prosencephalic alar plate in land vertebrates, the pallial area considered homologous to the hippocampus in teleost fish is the dorsolateral telencephalic region [158,159,170,171,172,173].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [158]
The telencephalon of ray-finned fishes (actinopterygians) contains a region homologue to the hippocampus of tetrapods.
“Interestingly, comparative neurobiological research shows that the telencephalon of ray-finned fishes (actinopterygians) can also contain a region homologue to the hippocampus of tetrapods [158,159].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [158]
Along with the evolutionary appearance of placodes and neural crest came the enlarged brain of craniates, with a complete craniate forebrain, midbrain, and hindbrain.
“In summary, along with the evolutionary appearance of placodes and neural crest came the enlarged brain of craniates, well beyond that seen in the protochordates, with a complete craniate forebrain, midbrain, and hindbrain.”
From The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago (2013) · cites this paper as Butler and Hodos, 2005
The telencephalon may require a fully developed olfactory placode for its induction, which would imply that Haikouella had only a tiny or non-existent olfactory placode; only hints of olfactory capsules and nostrils are seen in the adult fossils.
“This brain region may require a fully developed olfactory placode for its induction (Butler, 2000, 2006; Butler and Hodos, 2005), which would imply that Haikouella had only a tiny or non-existent olfactory placode; indeed, only hints of olfactory capsules and nostrils are seen in the adult fossils.”
From The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago (2013) · cites this paper as Butler and Hodos, 2005
There was a transitional animal between a cephalochordate-like ancestor and the first true craniates, called a 'cephalate'.
“She proposed that there was a transitional animal between a cephalochordate-like ancestor and the first true craniates, which she called a “cephalate” (a combination of the words “cephalochordate” and “craniates”).”
From The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago (2013) · cites this paper as Butler and Hodos, 2005
Butler hypothesized that the advent of an advanced visual system played an early and critical role in the formation of the vertebrate brain.
“In her intriguing scenario of the evolution of vision and the brain, Butler (Butler, 2000, 2006; Butler and Hodos, 2005) hypothesized how the advent of an advanced visual system played an early and critical role in the formation of the vertebrate brain.”
From The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago (2013) · cites this paper as Butler and Hodos, 2005
The transition from cephalochordate to craniate was sequential, beginning with the establishment of paired, lateral eyes and optic nerves followed by elaboration of the descending visual pathway to brainstem motor centers.
“According to this account, the transition from cephalochordate to craniate was sequential, beginning with the establishment of paired, lateral eyes and optic nerves followed by elaboration of the descending visual pathway to brainstem motor centers.”
From The evolutionary and genetic origins of consciousness in the Cambrian Period over 500 million years ago (2013) · cites this paper as Butler and Hodos, 2005
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Marhounová, L., Kotrschal, A., Kverková, K., Kolm, N., & Němec, P. (2019) · Evolution · doi:10.1111/evo.13805 · Cited by 67 · see citing works
Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions
Domínguez, L., Morona, R., González, A., & Moreno, N. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23222 · Cited by 65 · see citing works
- Authors
- Butler, A. B., & Hodos, W.
- Venue
- Wiley eBooks
- Publisher
- Wiley
- Published
- 2005-08-09
- OpenAlex
- W4245560018
- Cited by
- 640
- References
- 0
- Citations by year
- 2026: 25 · 2025: 21 · 2024: 18 · 2023: 22 · 2022: 31 · 2021: 43 · 2020: 27 · 2019: 41 · 2018: 26 · 2017: 39 · 2016: 28 · 2015: 31 · 2014: 27 · 2013: 25 · 2012: 29
- FWCI
- 38.52
- Type
- book
- Language
- en
- Open access
- closed
- Locations
- Wiley eBooks (publishedVersion)
- Topics
- Health Sciences › Medicine › Urology › Comparative Animal Anatomy Studies
- Health Sciences › Medicine › Anatomy › Medical and Biological Sciences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Undergraduate Neuroscience Education and Research
- Keywords
- brain evolution, comparative neuroanatomy, brain structure, vertebrate phylogeny
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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