. Chordate morphology. Morphology (Animals); Chordata. TELEOST OR POLYPTERUS ACIPENSER Figure 13-5. Cross sections of cerebral hemispheres of different vertebrates with suggested path- ways of evolution. 1, hippocampus; 2, general pallium (neopallium); 3, pyriformts; 4, lateral olfac- tory nucleus (striate body); 5 tuberculum olfactorium (polaeopollium); 6, septal nuclei; ventricular layer of nuclei cross hatched. (Moinly after Rudebeck, 1945) CHIMAERID fore the cerebral lobes. Basically the cerebral lobes are ol- factory lobes, but have incipient higher centers. The diencephalon has a pineal
![. Chordate morphology. Morphology (Animals); Chordata. TELEOST OR POLYPTERUS ACIPENSER Figure 13-5. Cross sections of cerebral hemispheres of different vertebrates with suggested path- ways of evolution. 1, hippocampus; 2, general pallium (neopallium); 3, pyriformts; 4, lateral olfac- tory nucleus (striate body); 5 tuberculum olfactorium (polaeopollium); 6, septal nuclei; ventricular layer of nuclei cross hatched. (Moinly after Rudebeck, 1945) CHIMAERID fore the cerebral lobes. Basically the cerebral lobes are ol- factory lobes, but have incipient higher centers. The diencephalon has a pineal Stock Photo](https://c8.alamy.com/comp/RJ6T8X/chordate-morphology-morphology-animals-chordata-teleost-or-polypterus-acipenser-figure-13-5-cross-sections-of-cerebral-hemispheres-of-different-vertebrates-with-suggested-path-ways-of-evolution-1-hippocampus-2-general-pallium-neopallium-3-pyriformts-4-lateral-olfac-tory-nucleus-striate-body-5-tuberculum-olfactorium-polaeopollium-6-septal-nuclei-ventricular-layer-of-nuclei-cross-hatched-moinly-after-rudebeck-1945-chimaerid-fore-the-cerebral-lobes-basically-the-cerebral-lobes-are-ol-factory-lobes-but-have-incipient-higher-centers-the-diencephalon-has-a-pineal-RJ6T8X.jpg)
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. Chordate morphology. Morphology (Animals); Chordata. TELEOST OR POLYPTERUS ACIPENSER Figure 13-5. Cross sections of cerebral hemispheres of different vertebrates with suggested path- ways of evolution. 1, hippocampus; 2, general pallium (neopallium); 3, pyriformts; 4, lateral olfac- tory nucleus (striate body); 5 tuberculum olfactorium (polaeopollium); 6, septal nuclei; ventricular layer of nuclei cross hatched. (Moinly after Rudebeck, 1945) CHIMAERID fore the cerebral lobes. Basically the cerebral lobes are ol- factory lobes, but have incipient higher centers. The diencephalon has a pineal evagination which generally lacks an eye at its tip; a pineal nerve is lacking. In the frog a pineal eye is present and the pineal sac has in part lost con- nection with the brain (Figure 13-7). Anterior to the pos- terior commissure is a saccus dorsalis which in front culmi- nates in a paraphysis. Paraphysis and roof are much thickened as a chorioid plexus from which fingers of tissue extend down into the third ventricle and through the foramina of Monroe into the telencoels. A distinct velum transversum is lacking. The optic nerves decussate in entering the brain and some fibers of each optic tract synapse at a lateral geniculate nucleus with neurons leading to the cerebrum. The reduced eyes o{ Necturus are reflected by the relatively smaller optic lobes, as compared with the frog. The amphibian brain is peculiar in having a greatly re- duced cerebellum which is no more than a transverse band of tissue anterior to the chorioid plexus in the roof of the medulla. The cranial nerves of the amphibian resemble those of the preceding groups (Figure 13-8). The seventh has a super- ficial ophthalmic branch in salamanders but not in anu- THE CONDUCTING AND INTEGRATING SYSTEM • 389. Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the