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PubMed1987

Sound reception in two anabantid fishes.

1. Pure tone displacement sensitivity and bandwidth were measured from the saccule of the ear in two anabantid species (Trichogaster trichopterus and Helostoma temincki) using microphonic potentials with a 1 microV RMS threshold for the second harmonic of the stimulus frequency. 2. Saccular microphonics were recorded in both species from 80 to 1600 Hz, with lowest thresholds between 100 and 200 Hz. The overall microphonic response curves (sensitivity and bandwidth) of the two species were statistically similar to one another with an analysis of variance, although there were statistically different thresholds at 100 and 800 Hz. 3. The hair cell orientation patterns of the saccular epithelia differ in the two species. Consequently, the comparative sizes of the saccular sensory epithelium and numbers of sensory hair cells were examined. The saccular sensory epithelium of Helostoma is about 40% larger and contains nearly 50% more hair cells than the saccular epithelium of a comparably sized Trichogaster. 4. An extracranial air bubble, located in the suprabranchial chamber, is found in both species. The bubble has direct access to the saccular chamber in Trichogaster through a foramen which is absent in Helostoma. Despite the difference in morphology and the larger numbers of sensory hair cells in Helostoma, hearing sensitivity and bandwidth is similar in the two species. Although the structural differences in the auditory periphery do not affect pure tone sensitivity and bandwidth, other aspects of fish hearing such as frequency discrimination, discrimination of signals in the presence of noise, and/or sound localization ability may be affected by these structural differences.

Acoustic Stimulation↗
PubMed1993

Implicit memory for stimuli presented during anaesthesia: role of anaesthetic cocktail and memory test.

Recently, investigators have used so-called implicit memory tests to investigate 'hearing' during general anaesthesia. Some of them were able to demonstrate auditory perception in anaesthetized patients, but others have failed to find any evidence for intraoperative stimulus registration. We argue that differences in anaesthetic cocktails and memory tests can explain why some researchers have produced positive results, supportive of information-processing under anaesthesia, and others have not. It appears that stimulus registration can occur during surgery, regardless of anaesthetic technique. However, processing of complex information may only be possible during nitrous oxide anaesthesia.

Acoustic Stimulation↗
PubMed1980

Relations between frequency selectivity and two-tone rate suppression in lizard cochlear-nerve fibers.

Cochlear-nerve fibers innervating the apicial region of the alligator lizard basilar papilla show sharp frequency selectivity in response to single tones (measured with the frequency threshold contour, or FTC), and the phenomenon of two-tone rate suppression (TTRS) in response to two simultaneously presented tones (measured with the iso-TTRS contour, or ITC). The gross shapes of the FTCs, as characterized by the slopes of the sides and Q10dB, vary systematically with the fiber's characteristic frequency (CF). 'Fine-structural' features are also found: below CF, notches (frequency regions of relatively high threshold) occur in the FTC at frequencies related to CF. Above CF, a break frequency, which varies with CF, divides the FTC into segments of different slope. Features of the ITC also vary with CF. The detailed shapes of the FTCs and ITCs are related: lobes of the ITC interdigitate with notches in the FTC; the side of the FTC with steepest slope is closely associated with the side of the ITC with steepest slope. The close relation that is observed between sharp frequency selectivity and TTRS suggests that both phenomena arise from a common cochlear mechanism.

Acoustic Stimulation↗
PubMed1980

Encoding of alternating acoustical signals in the medial geniculate body of guinea pigs.

In unanaesthetized guinea pigs 102 single units of the medial geniculate body were recorded under acoustical stimulation with alternating noise and tone impulses. The temporal parameters of the signals were chosen in close relation to psychoacoustical pulsation-threshold measurements. Most units showed a strong interaction between the responses of the non-simultaneously presented signal components (temporal suppression). The phasic part of each impulse-evoked response was more affected by the suppression than the tonic part. Thus, two regions of responsiveness could be verified: a region of pure tonic discharge and a region of tonic and phasic discharge. The borderline between both regions was defined as 'on-threshold'. The temporal suppression effect of the discharge rate did depend on impulse duration, impulse shape, gap duration, and the levels of the signal components. The overall unit-response characteristic-especially the lac of temporal onset information--suggested a close relation between psychoacoustical pulsation threshold and physiological 'on-threshold'.

Acoustic Stimulation↗
PubMed1980

Processing of noise by single units of the inferior colliculus of the bar Rhinolophus ferrumequinum.

For inferior colliculus units the response patterns and the thresholds for pure tones and noise of variable bandwidth were determined. In a threshold-bandwidth plot the noise thresholds usually fell along two regression lines whose point of intersection established the size of the neuronal critical bandwidth (nCB). The relevance of the small nCBs (0.2-0.4 kHz) obtained for the frequency range of the constant frequency part of the orientation call is discussed. No fixed relation was found either between the nCBs and the neuronal critical ratios or between the size of nCB and the width of the tuning curve 3 dB above threshold of the best frequency.

Animals↗
PubMed1981

Responses of single neurons in physiologically defined area AI of cat cerebral cortex: sensitivity to interaural intensity differences.

In 15 cats, cortical area AI was defined by its frequency organization, and cells within that field were tested for sensitivity to interaural intensity differences (IIDs) using sealed stimulus delivery systems. Of 39 cells tested quantitatively, 26 were sensitive to IIDs. In 70% of cases, sensitivity to IIDs reflected suppressive binaural interactions, and was manifested as a sigmoidal relation of spike count to IID. For 8 other cells, facilitative binaural interactions generated unit sensitivity to IIDS; three of these neurons demonstrated nonmonotonic dependency of spike count on IID, with peak firing rates at or near 0 dB IID. Analysis of spike count versus IID functions in terms of the auditory azimuths known to generate the IIDs used revealed that the majority of cells were most sensitive to IIDs associated with azimuths in the contralateral sound field. These data are compatible with other evidence on the sensitivity of cortical and brainstem cells to binaural sound localization cues, and suggest that each side of the auditory brain is independently capable of localizing sound sources in the contralateral field.

Animals↗
PubMed1981

The phonochrome: a coherent spectro-temporal representation of sound.

Representation of simple stationary sounds can be given either in the temporal form by display of the waveform as function of time or in the spectral form by intensity and phase as function of frequency. For complex nonstationary sounds, e.g. animal vocalisations and human speech, a combined spectro-temporal representation is more directly associated with auditory perception. The well-known sonogram or dynamic power spectrum has a fixed spectro-temporal resolution and neglects phase relations of different spectral and temporal sound components. In this paper the complex spectro-temporal intensity density CoSTID) is presented as a coherent spectro-temporal image of a sound, based on the analytic signal representation. The CoSTID allows an arbitrary form of the spectro-temporal resolution and preserves phase relations of different sound components. Since the CoSTID is a complex function of two variables, it leads naturally to the use of colour images for the spectro-temporal representation of sound: the phonochrome. The phonochromes are shown for different technical and natural sounds. Applications of this technique for study of phonation and audition and for biomedical signal processing are indicated.

Acoustics↗
PubMed1982

The phase angle of addition in temporal masking for diotic and dichotic listening conditions.

The phase angle, alpha, between a tonal signal and a tonal masker was varied from 0 degrees to 135 degrees in simultaneous masking, forward masking, and pulsation-threshold paradigms. In all conditions the frequency of the signal and masker was 500 Hz. For forward masking both diotic (MOSO) and dichotic (MOS pi) listening conditions were investigated. Only the dichotic case was studied using the pulsation threshold method. In simultaneous masking, thresholds varied as a function of alpha in both diotic and dichotic conditions. Thresholds in the diotic conditions were consistently different from those in the dichotic conditions -- i.e., there were masking-level differences (MLDs) at most values of alpha tested. In forward masking and pulsation-threshold, however, thresholds were independent of alpha in the dichotic conditions; and thresholds were independent of alpha in the diotic, forward masking conditions. Nevertheless, for forward masking the dichotic thresholds remained below the diotic thresholds, yielding MLDs of 3-6 dB. Thus, in nonsimultaneous masking, there is a clear effect of the interaural signal phase, but not of the masker-signal phase relationship, on signal detectability. These results imply that masker-signal phase information is either not preserved or not used by subjects in nonsimultaneous tone-on-tone masking experiments.

Auditory Perception↗
PubMed1983

Neural mechanisms in sound detection and temporal summation.

The psychophysics and neurophysiology of sound detection in quiet and under noise masking were studied in goldfish. Psychophysical masking is a linear function of masker level. For long duration signals, signal-to-noise ratios (S/N) at threshold are 15.5, 19, and 22.5 dB for 200, 400 and 800 Hz signals, respectively, and is -5 dB for a noise signal. Threshold declines with signal duration to about 700 ms. The slopes of the masked temporal summation functions are about unity, indicating that energy is constant at threshold. In quiet however, the slopes are generally less than 0.5, indicating that shorter signals are detected at lower energy. Neural correlates of the masked S/Ns and the slopes of temporal summation functions were sought in the response patterns of single saccular neurons. Rate- and synchronization-intensity functions were obtained for tone and noise signals in quiet and in noise. S/Ns at behavioral threshold correspond closely to those required to raise spike rate just above that evoked by the masker alone, but are well above those required to cause clear synchronization. Therefore, sound detection is probably based on spike rate and not synchronization criteria. The equivalence of behavioral and neural thresholds indicates that the filters used in behavioral sound detection are simply the bandwidths of saccular fibers. A model outlined by Zwislocki which predicts the rate of temporal summation from the rate of growth of neural activity with intensity accounts quite well for the observed slopes of temporal summation functions both in quiet and in noise.

Action Potentials↗
PubMed1983

Psychophysics and neurophysiology of repetition noise processing in a vertebrate auditory system.

The psychophysics and neurophysiology of repetition noise (RN) processing was studied in the goldfish. RN is the sum of a noise waveform with its delayed (by T s) repetition, which may be attenuated (by A dB), and inverted relative to the undelayed signal. Such a signal has a periodic spectrum with peaks separated by 1/T Hz, and a prominence in its autocorrelation function at T s. In usual environments, RN contains information about sound-reflecting surfaces. Delays in the range of 0.5-20 ms create pitch sensations in man. Psychophysical experiments using classical respiratory conditioning investigated the masking effectiveness of RN on tones, the detection of changes in delay (T) at various values of T, A and overall noise level, and the values of A required to bring a 20% delay discrimination to threshold. While the masking data define detection filters quite broadly tuned compared with man, various measures of delay discrimination are comparable to those for man. Unit responses from the auditory nerve are consistent with broadly tuned psychophysical filters, but in all cells studied show prominent inter-spike-interval (ISI) peaks which predict the delay values used to generate the RN. We conclude that the qualitative features of RN are coded in ISIs, and are processed by the CNS in the time domain. Similar mechanisms may be used by other vertebrate species in processing repetition noise.

Animals↗
PubMed1985

A functional organization of binaural responses in the inferior colliculus.

Binaural responses are segregated within an enlarged isofrequency region of the mustache bat's inferior colliculus. In the part of this region containing E-I responses, there is an orderly shift in the sensitivity of unit clusters to interaural intensity disparities, having implications for the representation of auditory space within isofrequency regions of the inferior colliculus.

Animals↗
PubMed1985

Binaural interactions in cortical area AI of cats reared with unilateral atresia of the external ear canal.

Binaural interactions were recorded in auditory cortical (AI) neurons of anesthetized adult cats that had unilateral atresias created shortly after birth by surgically ligating and cutting one external ear canal. At the time of the recording experiment, the atresia and associated debris were removed and tones were delivered to both tympanic membranes via a sealed and calibrated acoustic system. The majority of neurons recorded were in the cortex ipsilateral to the previously occluded ear. Thresholds for monaural stimulation of either the operated or unoperated ear were within normal range although thresholds to stimulation of the previously operated ear tended to occupy the upper end of the normal distribution. Monotonic and nonmonotonic spike count-vs-intensity functions derived from responses to monaural stimulation of the atretic ear were indistinguishable in their shape from those recorded in normal cats. All binaural classes were represented in our sample in proportions similar to those reported in cats with two normal ears. The forms of the functions relating spike count to interaural intensity differences and interaural phase differences were essentially the same as those seen in normal animals. The main binaural deficit observed under these conditions was a shift in the interaural intensity difference to which an AI neuron was most sensitive. The intensity needed for a stimulus to the atretic ear to participate in the binaural response was as much as 50 dB higher than that at the opposite normal ear in contrast to the nearly equal SPLs required for binaural interactions in cats with two ears intact. It was suggested that elevated thresholds at the previously operated ear could account for much of the shift observed.

Action Potentials↗
PubMed1985

A monaural space map in the guinea-pig superior colliculus.

Under anechoic conditions, a horizontal array of loudspeakers was used to investigate the representation of auditory space in the guinea-pig superior colliculus. We have previously demonstrated that in animals with both ears intact, there is a topographical representation of the azimuthal dimension of auditory space in the deep layers of this nucleus. In the present study, we have investigated the contribution of monaural and binaural cues to the generation of the auditory space map. Occlusion of one ear or unilateral cochlear destruction resulted in omnidirectional responses in all cells to white-noise stimuli more than 20 dB suprathreshold. The sensitivity of cells to the location of sound at or near threshold was, however, unchanged and we demonstrate the presence of a threshold, monaural auditory space map. This monaural space map was destroyed by removal of the contralateral pinna and concha which resulted in all cells responding best, at threshold, to sounds opposite the external auditory meatus. Measurements of cochlear microphonic (CM) potentials, although variable, revealed that the pinna and concha may result in location-specific changes in the spectral pattern at the tympanic membrane.

Animals↗
PubMed1985

Sound localization in wild Norway rats (Rattus norvegicus).

The ability of three wild Norway rats to localize sound was determined for single clicks and 100-ms white noise bursts. Chance level localization thresholds were 12 degrees for clicks and 9.7 degrees for white noise. A comparison of these results with published localization thresholds for the domestic albino rat yielded no significant differences. It appears that the combined effects of domestication and albinism have not affected the ability of the laboratory rat to localize sound. Instead, the relatively poor localization acuity of these rats appears to be part of the normal variation in sound localization acuity found among different species of mammals.

Animals↗
PubMed1986

The acoustic middle ear muscle reflex in albino rats.

The acoustic middle ear muscle reflex was studied in albino rats anesthetized with chloralose. The best frequency of the reflex and the threshold at this frequency were on average about 3 kHz and 57 dB SPL, respectively. The threshold increased as frequency increased above, and decreased below, the best frequency at a rate of about 20 dB/octave. Above about 12 kHz, the muscular response showed instability and habituation. Thresholds were similar between stapedius and tensor tympani reflexes and between ipsilateral and contralateral reflexes. The middle ear transmission loss due to the reflex was the greatest and nearly constant below about 1 kHz, where the loss was about 18 dB at the maximal stimulation. Above this frequency the loss decreased as frequency increased up to 20 kHz. Thus the reflex, unlike that in other animals, suppressed transmission over the whole range of reflex-eliciting frequencies. The transfer function of the reflex had a well damped low-pass characteristic with a cut-off frequency of about 20 Hz. From the above characteristics of the reflex, the role of the rat's tympanic muscles in improving ultrasonic hearing under ambient noises was suggested.

Animals↗
PubMed1987

The maturation of the central auditory conduction in preterm infants until three months post term. II. The auditory brainstem responses (ABRs).

Auditory evoked brainstem responses (ABRs) were recorded in 65 preterm infants (serially in 55 of them), divided into 5 groups, according to their gestational age (GA). The recording sessions were performed at 8 conceptional age levels (CA = GA + chronological age), of which the last two were about 40 and 52 weeks CA. The number of recording sessions varied from one to seven. A full set of ABR latency and amplitude parameters was analyzed including peaks I, II, IIN, III, V and IIc, IIINc and Vc as well as some interpeak latency differences (IPLDs), and the amplitude ratios. The detectability of the different components in the ABR tests at 70 dB reached 80-100% at about 32 weeks CA. The side of stimulation nor the state of vigilance influences the detectability. The degree of prematurity in the 5 GA groups did not influence the development of the parameters. Neither the side of stimulation nor generally the state of vigilance give rise to different parameter values. The thresholds show an age dependent decrease, which is also determined by central maturation. The differential development of the latency decrease of the ABR parameters with increasing conceptional age can be associated with morphological maturational processes and may add weight to the arguments in the delineation of the sources of the ABR. The ipsi- and contralateral central conduction V-II and Vc-IIc do not show latency differences at any CA level. The components IIc and Vc, however, lagged behind in absolute latency compared with II and V. It is concluded that the ABR is a powerful instrument for the study of the maturation of the human auditory pathway in the brainstem. In view of the variability, the detectability and the complex changes within the ABR during the preterm period, its application for clinical purposes during this period has a limited value.

Analysis of Variance↗
PubMed1987

Some physical and psychological effects produced by selective delays of the envelope of narrow bands of noise.

One can construct narrow bands of noise that contain delays of either the envelope, the phase, or the carrier separately or in combination. Delayed and undelayed noises will have identical spectra if, and only if, both the envelope and the phase undergo delays of the same magnitude. To study lateralization of these signals, an acoustic pointing task was employed in which listeners varied the interaural intensitive disparity of a narrow band of noise (the pointer) so that it matched the position of a second, experimenter-controlled stimulus (the target) which contained symmetric interaural delays of only the envelope. Targets were narrow bands of noise with center frequencies chosen at octave intervals between about 500 Hz and about 4000 Hz. The smallest bandwidth was 100 Hz and the largest was 800 Hz. For high-frequency stimuli, delays of only the envelope of a narrow band of noise appear to mediate lateralization which is greatest for bands centered near 2000 Hz. For low frequencies, delays larger than 800 microseconds were required to produce acoustic images appreciably away from the midline. These findings confirm the notion that listeners are sensitive to interaural temporal disparities in the envelopes of high-frequency, complex stimuli.

Acoustic Stimulation↗