Research paperA functional map of the pigeon basilar papilla: correlation of the properties of single auditory nerve fibres and their peripheral origin
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2022, Sturkie's Avian PhysiologyAnimals models of hidden hearing loss: Does auditory-nerve-fiber loss cause real-world listening difficulties?
2022, Molecular and Cellular NeuroscienceCitation Excerpt :Rather than having distinct inner and outer hair cells as in mammals, avian hair-cell shape changes gradually across the width of the sensory epithelium from tall to short, with tall hair cells located closest to the auditory-nerve ganglion and receiving primarily afferent synaptic innervation with up to four synapses per hair cell. Short hair cells are thought to supply cochlear amplification and receive primarily efferent synaptic input (Gleich, 1989; Köppl et al., 2000; Smolders et al., 1995). Despite these anatomical differences, the avian cochlea is tonotopic and avian auditory-nerve fibers show fundamentally similar response properties to those of mammals, including V-shaped frequency tuning curves, limited dynamic range of rate-level functions, and phase-locking up to a maximum frequency of several kHz (Gleich, 1989; Manley et al., 1985; Sachs et al., 1974; Salvi et al., 1992).
Suppression tuning of spontaneous otoacoustic emissions in the barn owl (Tyto alba)
2020, Hearing ResearchCitation Excerpt :Moreover, the inner ear of the barn owl is complex and large, being 12 mm long (Fischer et al., 1988). In most birds, such as pigeons (Smolders et al., 1995) or chickens (Fischer, 1992), the basilar papillae are only approximately 5 mm long. The auditory sensitivity range of the barn owl ear covers about 5 octaves.
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2015, Sturkie's Avian Physiology: Sixth EditionUsing frequency ratios to study vocal communication
2013, Animal BehaviourExperiments in comparative hearing: Georg von Békésy and beyond
2012, Hearing ResearchCitation Excerpt :A smaller difference (and in the other direction!) exists between BM and neural measurements in the pigeon cochlea (Fig. 2D; Gummer et al., 1987; Smolders et al., 1995). We now know that when measured under very loud or hypoxic conditions or before the active process has developed during ontogeny, the best response frequency of any given cochlear location in mammals is shifted toward lower frequencies (e.g., Arjmand et al., 1988).