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The medial cortex of reptiles does not appear to be involved in other tasks that are mediated by the hippocampus of mammals.

The contralateral component of lemnothalamic-pallial projections (present to a substantial degree in amphibians, birds and reptiles, and, to a minor degree, in mammals) is omitted.

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The locations of the reptile bones and the productive palynological samples are shown.

In light of these findings, reptile meat should not be excluded as a potential source of human trichinellosis.

Schematic sequence of developmental events resulting in the specification of the main anterior telencephalic regions in reptiles and mammals, viewed in the coronal plane.

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An example is the anatomy shared by reptiles and mammals, which is evidence of shared ancestry.

I begin with the so-called lower vertebrates - the classes that evolved earlier and seem generally less complex - fishes, amphibians and reptiles.

This behaviour suggests that they use the vomeronasal system to locate reptile nests and rodent burrows by scent.

Therefore, the similarity between modern reptiles and mammals in the topology of these "cortical" sensory areas may be due to common inheritance from stem amniotes.

The paucity of the modern-day insular herpetofaunas is reflected in the fossil reptile diversity of the solution cavity fills found on the same islands.

In contrast, for sand and for loam soils, there is far more continuity and similarity in reptile species composition down the rainfall gradient.

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In spite of it being a pervasive projection among reptiles, it has not been considered in detail in any previous study.

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The reptiles and mammals found in the fissure deposits are found, most frequently, in the form of numerous disarticulated skeletal elements.

It is suggested that the dorsal cortex of reptiles expanded in this dorsalizing process to become both entorhinal/subicular cortex and sensory neocortex.

It is likely that the mammal-like reptiles emerged quite early from the ancestral amniote stock.

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