Frequency Selectivity, Adaptation, and Suppression in Goldfish Auditory Nerve Fibers

The acoustic portions of the fish ear are otolith organs (the saccule, lagena, and in some species, the utricle), which are specialized to respond to acoustic energy in the frequency range from below 100 Hz to 2 to 3 kHz in some species. These organs contain a sensory epithelium, made up of type II hair cells, a solid calcium carbonate otolithic stone, and an otolithic membrane intervening between the hair cell cilia and the otolith. In most fish species, sound can reach the ear and cause a displacement of the hair cell cilia through at least two pathways; a direct route through which acoustic particle motion is detected by the otolithic organs operating in an inertial “accelerometer” mode, and an indirect route through which the motion of a gas sac (e.g. swimbladder), as it expands and contracts with the sound pressure waveform, is efficiently transmitted to the ear. See Fay and Popper (1980) for a general review of fish hearing.

[1]  R. Fay,et al.  Phase-locking in goldfish saccular nerve fibres accounts for frequency discrimination capacities , 1978, Nature.

[2]  W. Brownell,et al.  Single unit analysis of the posteroventral cochlear nucleus of the decerebrate cat , 1982, Neuroscience.

[3]  Two-tone rate suppression in lizard cochlear nerve fibers, relation to receptor organ morphology , 1978, Brain Research.

[4]  I. J. Russell,et al.  Two-tone suppression in cochlear hair cells , 1979, Hearing Research.

[5]  T. Furukawa Sites of termination of the saccular macula of auditory nerve fibers in the goldfish as determined by intracellular injection of procion yellow , 1978, The Journal of comparative neurology.

[6]  E D Young,et al.  Excitatory/inhibitory response types in the cochlear nucleus: relationships to discharge patterns and responses to electrical stimulation of the auditory nerve. , 1985, Journal of neurophysiology.

[7]  M. Sachs,et al.  Two-tone inhibition in auditory-nerve fibers. , 1968, The Journal of the Acoustical Society of America.

[8]  D L Tomko,et al.  The neural signal of angular head position in primary afferent vestibular nerve axons , 1973, The Journal of physiology.

[9]  Lawrence S. Frishkopf,et al.  Responses to Acoustic Stimuli from Single Units in the Eighth Nerve of the Bullfrog , 1963 .

[10]  R. Fay Sound intensity processing by the goldfish. , 1985, The Journal of the Acoustical Society of America.

[11]  Geoffrey A. Manley,et al.  A Review of the Auditory Physiology of the Reptiles , 1981 .

[12]  E D Young,et al.  Discharge patterns of single fibers in the pigeon auditory nerve. , 1974, Brain research.

[13]  Sheryl Coombs,et al.  Neural mechanisms in sound detection and temporal summation , 1983, Hearing Research.

[14]  日本音響学会,et al.  Comparative Studies of Hearing in Vertebrates , 1980, Proceedings in Life Sciences.

[15]  W. S. Rhode,et al.  Some observations on cochlear mechanics. , 1978, The Journal of the Acoustical Society of America.

[16]  Axel Michelsen,et al.  Time Resolution in Auditory Systems , 1985, Proceedings in Life Sciences.

[17]  William A. Yost,et al.  Psychophysics and neurophysiology of repetition noise processing in a vertebrate auditory system , 1983, Hearing Research.