Effects of bilateral auditory cortical lesions on gap-detection thresholds in the ferret (Mustela putorius).

Ferrets were tested for their ability to detect temporal gaps in noise before and after bilateral lesions of the primary auditory cortex. Thresholds for gap detection were determined first for normal animals with band-pass noises at various center frequencies (0.5 to 32 kHz) and at 8 kHz with various sound pressure levels (-10-70 dB). Gap-detection ability improved steadily as sound pressure increased up to 70 dB. No systematic relation was found between threshold and center frequency. To determine the effects of brain damage, ferrets were tested with 8-kHz band-pass noise at 70 dBSPL. After bilateral lesions of auditory cortex, ferrets were still capable of detecting gaps, but the mean threshold was elevated from 10.1 to 20.1 ms. The data demonstrate that auditory cortex is important for perceptual tasks requiring fine temporal resolution.

[1]  E. Bullmore,et al.  Society for Neuroscience Abstracts , 1997 .

[2]  W. R. Howse,et al.  Auditory temporal resolution: effects of sensation level. , 1978, The Journal of auditory research.

[3]  D Henderson,et al.  Gap detection in hearing-impaired chinchillas. , 1982, The Journal of the Acoustical Society of America.

[4]  H. Buchtel,et al.  Auditory agnosia: Apperceptive or associative disorder? , 1989, Brain and Language.

[5]  T. Imig,et al.  Thalamic projections to fields A, AI, P, and VP in the cat auditory cortex , 1987, The Journal of comparative neurology.

[6]  L. Aitkin,et al.  Azimuthal sensitivity of neurons in primary auditory cortex of cats. II. Organization along frequency-band strips. , 1990, Journal of neurophysiology.

[7]  K M Heilman,et al.  Pure word deafness after bilateral primary auditory cortex infarcts , 1984, Neurology.

[8]  R. Plomp Rate of Decay of Auditory Sensation , 1964 .

[9]  D. P. Phillips,et al.  Neurons in the cat's primary auditory cortex distinguished by their responses to tones and wide-spectrum noise , 1985, Hearing Research.

[10]  D. P. Phillips,et al.  Response timing constraints on the cortical representation of sound time structure. , 1990, The Journal of the Acoustical Society of America.

[11]  H. Heffner,et al.  Effect of bilateral auditory cortex lesions on sound localization in Japanese macaques. , 1990, Journal of neurophysiology.

[12]  R J Salvi,et al.  Gap detection in chinchillas with temporary high-frequency hearing loss. , 1985, The Journal of the Acoustical Society of America.

[13]  D P Phillips,et al.  Auditory temporal resolution in multiple sclerosis. , 1994, The Journal of otolaryngology.

[14]  C. Schreiner,et al.  Representation of amplitude modulation in the auditory cortex of the cat. II. Comparison between cortical fields , 1988, Hearing Research.

[15]  M. J. Penner Persistence and integration: Two consequences of a sliding integrator , 1975 .

[16]  S. Shamma,et al.  Organization of response areas in ferret primary auditory cortex. , 1993, Journal of neurophysiology.

[17]  D. Perrott,et al.  Auditory temporal resolution: Gap detection as a function of interpulse frequency disparity , 1971 .

[18]  J. Ison Temporal acuity in auditory function in the rat: reflex inhibition by brief gaps in noise. , 1982, Journal of comparative and physiological psychology.

[19]  J. Kelly,et al.  Midline and lateral field sound localization in the ferret (Mustela putorius): contribution of the superior olivary complex. , 1992, Journal of neurophysiology.

[20]  P. Fitzgibbons,et al.  Temporal gap detection in noise as a function of frequency, bandwidth, and level. , 1983, The Journal of the Acoustical Society of America.

[21]  D. P. Phillips,et al.  Acquired word deafness, and the temporal grain of sound representation in the primary auditory cortex , 1990, Behavioural Brain Research.

[22]  R. J. Irwin,et al.  Temporal acuity in normal and hearing-impaired listeners. , 1981, Audiology : official organ of the International Society of Audiology.

[23]  M. Merzenich,et al.  Role of cat primary auditory cortex for sound-localization behavior. , 1984, Journal of neurophysiology.

[24]  M J Penner,et al.  Detection of temporal gaps in noise as a measure of the decay of auditory sensation. , 1976, The Journal of the Acoustical Society of America.

[25]  Phillips Dp Central auditory processing: a view from auditory neuroscience. , 1995, The American journal of otology.

[26]  T. Imig,et al.  Binaural columns in the primary field (A1) of cat auditory cortex , 1977, Brain Research.

[27]  P J Fitzgibbons Temporal gap resolution in narrow-band noises with center frequencies from 6000-14000 Hz. , 1984, The Journal of the Acoustical Society of America.

[28]  M. Merzenich,et al.  Frequency representation in auditory cortex of the common marmoset (Callithrix jacchus jacchus) , 1986, The Journal of comparative neurology.

[29]  W. Jenkins,et al.  Sound localization: effects of unilateral lesions in central auditory system. , 1982, Journal of neurophysiology.

[30]  T. Imig,et al.  Organization of the thalamocortical auditory system in the cat. , 1983, Annual review of neuroscience.

[31]  B. Yaqub,et al.  Pure word deafness (acquired verbal auditory agnosia) in an Arabic speaking patient. , 1988, Brain : a journal of neurology.

[32]  J. Kelly,et al.  Contribution of auditory cortex to sound localization by the ferret (Mustela putorius). , 1987, Journal of neurophysiology.

[33]  J. Kelly,et al.  Hearing in the ferret (Mustela putorius): effects of primary auditory cortical lesions on thresholds for pure tone detection. , 1988, Journal of neurophysiology.

[34]  D. P. Phillips,et al.  Representation of the cochlea in primary auditory cortex of the ferret (Mustela putorius) , 1986, Hearing Research.

[35]  Jos J. Eggermont,et al.  Rate and synchronization measures of periodicity coding in cat primary auditory cortex , 1991, Hearing Research.

[36]  J. Kelly,et al.  Sound localization after unilateral lesions of inferior colliculus in the ferret (Mustela putorius). , 1994, Journal of neurophysiology.

[37]  P. Fitzgibbons,et al.  Gap detection in normal and hearing-impaired listeners. , 1982, The Journal of the Acoustical Society of America.

[38]  J. Ison,et al.  Temporal resolution of gaps in noise by the rat is lost with functional decortication. , 1991, Behavioral neuroscience.

[39]  D P Phillips,et al.  Effect of tone-pulse rise time on rate-level functions of cat auditory cortex neurons: excitatory and inhibitory processes shaping responses to tone onset. , 1988, Journal of neurophysiology.

[40]  M. Merzenich,et al.  Representation of the cochlear partition of the superior temporal plane of the macaque monkey. , 1973, Brain research.

[41]  J. B. Kelly,et al.  Primary auditory cortex in the ferret (Mustela putorius): neural response properties and topographic organization , 1988, Brain Research.

[42]  J. Kelly,et al.  Hearing in the ferret (Mustela putorius): Thresholds for pure tone detection , 1986, Hearing Research.

[43]  D. P. Phillips,et al.  Representation of acoustic events in the primary auditory cortex. , 1993, Journal of experimental psychology. Human perception and performance.

[44]  M M Merzenich,et al.  Representation of cochlea within primary auditory cortex in the cat. , 1975, Journal of neurophysiology.

[45]  D. S. Leitner,et al.  Parameters affecting gap detection in the rat , 1993, Perception & psychophysics.