NEURAL BASIS OF VIBRATION DETECTION IN LEPIDOSAURIAN REPTILES
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There are three potential pathways for detection of substrate vibration: cochlear, otolithic and somatosensory, reviewed in chapter one. How different lepidosaurian reptiles detect substrate vibration from these three pathways was explored from neuroanatomical and physiological perspectives. In chapter two, I described vibration sensitivity and the organization of the brainstem cochlear nuclei in the western snake (Pantherophis obsoletus). The western ratsnake is sensitive to low-frequency vibrations, comparable to other snakes. It has two first-order cochlear nuclei, nucleus magnocellularis (NM) and nucleus angularis (NA), similar to other reptiles. NM is small, while NA is relatively robust. In chapter three, I examined the connections and response properties of nucleus vestibularis ovalis (VeO) in the hindbrain of the tokay gecko (Gekko gecko). VeO receives input from the saccule, and connections of VeO mirror those of the cochlear nuclei, including an ascending projection to the central nucleus of the torus semicircularis. VeO neurons are sensitive to low-frequency vibration. In chapter four, I revisited a classic study to determine the connections and response properties of the snake torus semicircularis. In the western ratsnake, the torus can be divided into a central nucleus and a paratorus, the latter receiving input from the spinal cord, nucleus myelencephali dorsalis in the spinomedullary junction, as well as auditory nuclei. Toral neurons are sensitive to low frequency vibration and have heterogenous response characteristics. In chapter five, I discuss future directions based on findings in my dissertation and highlight the importance of vibration detection for lepidosaurs.