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Pitch is a fundamental perceptual attribute of sounds. Our ability to discriminate, separate, and identify sounds relies heavily on pitch. Recent neuroimaging studies in humans have provided converging evidence for the existence of a "pitch center"--a region on the superior temporal plane (STP) lateral to Heschl's gyrus specialized in pitch extraction--but a direct confirmation is still missing. Intracerebral recordings in humans are ideally suited for such a confirmation. Here we report results from depth electrode recordings in a patient undergoing investigation for epilepsy. We demonstrate a double dissociation between responses from the medial and lateral STP around Heschl's gyrus to the onset of sound energy and the onset of pitch. Three pieces of evidence support this finding: (1) the response to sounds that do not contain pitch is small in the lateral STP compared to the medial STP; (2) sounds that contain pitch evoke a strong response in the lateral STP; (3) at the transition from noise to a specialised noise-like, but tonal, sound referred to as iterated ripple noise, where the onset of pitch is the sole acoustic event, only the lateral contact showed a response. Our results provide direct evidence for a pitch-specific area on lateral STP with intracranial recordings from the human auditory cortex.

Introduction: Tinnitus is one of the most common symptoms in patients with profound sensorineural hearing loss (SNHL). Cochlear implantation (CI), which has become a standard method to rehabilitate profound SNHL, has been also observed to effect tinnitus in many cases. In the Salzburg Cochlear Implant Center,more than 230 profoundly deaf patients, mainly children,have been provided with CI between 1992 and 2000., Patients and Method: In a retrospective study, 39 adult patients were assessed by questionnaire for the frequency of tinnitus, subjective loudness sensitivity, and tinnitus-specific impairment before and after the CI., Results: Before implantation 26 patients had tinnitus, while 24 patients had the same symptoms after the CI. In 13 patients (50%) tinnitus remained unaffected by the operation. Intensity of tinnitus decreased in seven patients (26.7%), and in four patients (15.4%) it completely disappeared after the implantation.However, intensity increased in two patients (7.7%), and in another two patients, who had not experienced tinnitus before, it began first after the implantation. No correlation has been found between the daily using time of CI and the tinnitus impairment.Also no effect of tinnitus was seen on postoperative hearing assessed by Freiburg numbers, monosyllables, and Innsbruck sentence test scores., Conclusion: CI significantly reduces the subjectively perceived impairment, although the reduction in the subjectively perceived loudness of the tinnitus is not significant.

Human sound localization relies on binaural difference cues for sound-source azimuth and pinna-related spectral shape cues for sound elevation. Although the interaural timing and level difference cues are weighted to produce a percept of sound azimuth, much less is known about binaural mechanisms underlying elevation perception. This problem is particularly interesting for the frontal hemifield, where binaural inputs are of comparable strength. In this paper, localization experiments are described in which hearing for each ear was either normal, or spectrally disrupted by a mold fitted to the external ear. Head-fixed saccadic eye movements were used as a rapid and accurate indicator of perceived sound direction in azimuth and elevation. In the control condition (both ears free) azimuth and elevation components of saccadic responses were well described by a linear regression line for the entire measured range. For unilateral mold conditions, the azimuth response components did not differ from controls. The influence of the mold on elevation responses was largest on the ipsilateral side, and declined systematically with azimuth towards the side of the free ear. Near the midsagittal plane the elevation responses were clearly affected by the mold, suggesting a systematic binaural interaction in the neural computation of perceived elevation that straddles the midline. A quantitative comparison of responses from the unilateral mold, the bilateral mold and control condition provided evidence that the fusion process can be described by binaural weighted averaging. Two different conceptual schemes are discussed that could underlie the observed responses.

Category loudness scaling was used to investigate the loudness perception of 31 patients with a cochlear hearing loss (Group 1) by comparing the results with those found in 15 patients with retro-cochlear hearing loss caused by an acoustic neuroma (Group 2). Narrow-band noise signals at four different frequencies (0.5 to 4.0 kHz) were used. In the cochlear hearing-impaired subjects the slopes of the level-loudness functions tended to increase with increasing hearing loss, indicating positive recruitment, whereas the much shallower slopes associated with retro-cochlear lesions were presumed to reflect negative recruitment. The graphic representation of the iso-loudness functions revealed a different dynamic range between Group 1 and 2 with the ability to discriminate small differences of stimulus levels reduced in the presence of an acoustic neuroma. Category loudness scaling has been shown to be a valuable tool describing the individual perception of sound in a qualitative and quantitative manner. Furthermore, the method can be employed as an indicator of recruitment without any restrictive preconditions. For this reason the categorical loudness scaling can be a desirable method for supplementing the audiological diagnosis of a retro-cochlear hearing impairment through the frequency-specific description of a usable hearing-field and its dynamic range.

The functional development of the auditory system across metamorphosis was examined by recording neural activity from the torus semicircularis of larval and postmetamorphic bullfrog froglets in response to amplitude-modulated sound. Multiunit activity in the torus semicircularis during early larval stages showed significant phase-locking to the envelopes of amplitude-modulated noise bursts, up to modulation rates as high as 250 Hz. Beginning at metamorphic climax and continuing into the froglet period, phase locking was restricted to the more limited frequency range characteristic of adult frogs. The onset of operation of the tympanic pathway does not reinstate the highly synchronous neural activity characteristic of the operation of the fenestral pathway. Modulation transfer functions based on spike count did not show tuning for modulation rate in early stage tadpoles, but a greater variety of shapes of these functions emerged as development proceeded. Most of the different kinds of modulation transfer functions seen in adult frogs were also observed in froglets, but band-pass functions were not as sharply peaked. These data suggest that different neural codes for processing of the periodicity of complex signals operate in early stage tadpoles than in postmetamorphic froglets.

Periodic envelope or amplitude modulations (AM) with periodicities up to several thousand Hertz are characteristic for many natural sounds. Throughout the auditory pathway, signal periodicity is evident in neuronal discharges phase-locked to the envelope. In contrast to lower levels of the auditory pathway, cortical neurons do not phase-lock to periodicities above about 100 Hz. Therefore, we investigated alternative coding strategies for high envelope periodicities at the cortical level. Neuronal responses in the primary auditory cortex (AI) of gerbils to tones and AM were analysed. Two groups of stimuli were tested: (1) AM with a carrier frequency set to the unit's best frequency evoked phase-locked responses which were confined to low modulation frequencies (fms) up to about 100 Hz, and (2) AM with a spectrum completely outside the unit's frequency-response range evoked completely different responses that never showed phase-locking but a rate-tuning to high fms (50 to about 3000 Hz). In contrast to the phase-locked responses, the best fms determined from these latter responses appeared to be topographically distributed, reflecting a periodotopic organization in the AI. Implications of these results for the cortical representation of the perceptual qualities rhythm, roughness and pitch are discussed.

The present paper provides a brief review on topical issues of auditory physiology. Recent data on transduction mechanism and adaptation in hair cells as well as on the possible role of outer hair cells in amplifying basilar membrane motion are presented. Strategies of present physiological research in dealing with sensorineural deafness are discussed.

In a two-alternative forced-choice procedure lesser spear-nosed bats, Phyllostomus discolor, had to discriminate between a pure tone stimulus and a sinusoidally frequency-modulated signal generated at the same carrier frequency as the tone. Modulation depths of the SFM stimuli were reduced until the animals' performance dropped below the 75%-correct level which was used to determine difference limens for detection of frequency modulation (FMDL). The dependence of FMDLs on modulation and carrier frequency was systematically investigated. For a carrier frequency of 18.5 kHz, average FMDLs increased from 95 Hz at a modulation frequency of 10 Hz to 820 Hz at a modulation frequency of 2000 Hz which corresponds to Weber ratios (2 delta f/f) of 0.005 and 0.044 respectively. Further, difference limens were found to increase linearly in proportion to carrier frequency throughout a major part (9-74 kHz) of the species' hearing range. In comparison to other mammals, P. discolor has a pronounced capability for frequency discrimination which might be related to the extensive use of individually distinct frequency-modulated communication calls and audio-vocal learning.

Noise-induced temporary impairment of cochlear function was measured with several audiometric tests in order to evaluate which method best predicts a vulnerable cochlea. We tested 10 normally-hearing and 13 subjects who were positive for temporary threshold shifts (TTS). The latter were selected from 194 soldiers who demonstrated a TTS higher than 15 dB after regular training with firearms. Acoustic distortion products (DPOAE), click-evoked otoacoustic emissions (TEOAE), upper limit of hearing (ULH) and pure-tone and high-frequency audiometry were used to evaluate possible increased vulnerability of the cochlea. Tests were conducted at lower sound intensities (white noise, 90 dB SPL, 5 min; impact noise, 100 or 106 dB SPLs, 10 impulses/s, 5 min). Seventy per cent of the TTS-positive soldiers studied exhibited significant reductions of TEOAE amplitudes, whereas a stable emission was observed in all control subjects. DPOAE alterations were seen in 38% of the soldiers tested. These results indicate that TEOAE is the most sensitive, objective method for detecting a positive disturbance in cochlear function. Although the upper limit of hearing was also a very sensitive method, variability of this psychoacoustic method depended on the help and experience of the subjects being tested.

To investigate the dynamic properties of human hearing, experiments in vivo and with cadaver specimens can be carried out. Furthermore, electrical or mechanical models can also be used to study specific phenomena and parameter sensitivities. Present electrical and mechanical models are often based on crude structural and kinematic simplifications in which testing is restricted to static loading or simplified investigations. To investigate both static and dynamic behavior of normal and pathological ears spatial mechanical models have to be established. The different parts of sound transmission--i.e., airborne sound, elastic membranes, fluids, and ossicles have to be represented by different mechanical systems. In this investigations, a rigid body model of the middle ear was investigated. For verification, simulation results with respect to static loads were compared with measurements reported previously by Hüttenbrink. In further investigations, the dynamic behavior of the model will be evaluated. Models for the tympanic membrane and inner ear will also be formulated in order to create a compositive model that describes the whole hearing process. By so doing the successful development of prostheses as well as diagnostic methods will be supported.

Direct loudness scaling has been known as an audiological tool for about four decades. Although numerous publications have shown its clinical importance, loudness scaling has not been used in audiology and hearing aid fitting until now. This might be due to the lack of audiometers equipped with loudness scaling devices as well as missing evidence for its clinical applicability. In this study normal data for a single-step direct scaling procedure were established and loudness determinations of 105 patients with sensorineural hearing losses collected. The results show that normal level loudness functions exhibit very similar shapes for narrow band stimulation in the frequency range of 500 to 4000 Hz. However, loudness scaling is affected by the gender of the subjects: females scale systematically louder than do males. In hearing-impaired subjects the slopes of the level loudness functions tend to decrease with increasing hearing loss, indicating negative recruitment. This holds particularly true in the high-frequency range, e.g. at 4000 Hz. Our long-term experience with single-step direct loudness scaling has proven its clinical feasibility in typical patients of an audiology unit. Loudness scaling will prove useful for the localization of hearing impairments, as it can be employed as a quantitative indicator of recruitment without any restrictive preconditions. In addition, it allows the evaluation of hearing aids and cochlear implants by frequency-specific gain measurement.

The acoustic result following reconstruction of the middle ear is often disappointing and unpredictable. Apart from biologic factors, this is due to insufficient knowledge of the mechanism of sound transmission through the operated middle ear. Therefore, temporal bone experiments with simulated middle ear operations were set up to investigate the sound transmission following different prosthesis' designs, materials, etc. We developed a tiny hydrophone which has a frequency range from 100 Hz to 10 kHz in order to measure the sound pressure in the cochlear fluid. By comparing the sound pressure in the inner ear with the sound pressure at the drum membrane, we were able to analyze the transfer function of the manipulated middle ear. First results with different reconstruction techniques, prosthesis' designs and attachments demonstrated the usefulness of this measuring technique for the development of acoustically better middle ear reconstructions.

Distorsion product otoacoustic emissions (DPOAE) are generated by a continuous bitonal stimulation of the cochlea. The resulting emissions are measurable in a definite mathematical function of the primaries (mf1 +/- nf2; f1 < f2). In humans sound emission at the frequency 2f1-f are usually detectable. To determine if a disturbance of DPOAE-amplitude is associated with a cochlear lesion in the frequency region of the evoked emissions or the primaries, we performed suppression experiments using normal-hearing, healthy probands (n = 14). DPOAE were measured in the frequency range between 800 Hz and 8 kHz with different sound-pressure levels for the primaries. Evoked emissions for each proband were measured with these different stimulus parameters to determine baseline values. In suppression experiments sound emissions were evoked continuously with different stimuli between 800 Hz and 8 kHz, disturbed simultaneously with a third tone of 1, 2 and 4 kHz and then compared with baselines. Suppressor tones (1, 2, 4 kHz) reduced significantly the DPOAE amplitudes in the frequency region of the geometric mean of the primaries. This indicates that a reduction of the emission amplitude in associated with a cochlear lesion near the generation site of the DPOAE. The suppression curves exhibit a sharp and steep graph, indicating their relation to cochlear frequency selectivity.

Psychoacoustic tuning curves (PTC) can be regarded as filter curves, whereas their forms represent hair cell activity. Different influences--for example, noise, toxins, pharmacological causes and age--can change the PTC as a consequence of changed frequency selectivity without indication of deterioration in the audiogram. The objective of this investigation was to determine the visually perceivable change in the PTC as a quantifiable result. In so doing, the PTC was transformed into a hyperbola characterized by a parameter Q5. An example demonstrates the temporal change of Q5 under the influence of pharmacological drugs.

We investigated the influence of varying compliance of the tympanic membrane on the sound pressure level of the human ear canal using a model with adjustable compliance. Decrease of compliance augments the sound pressure close to the tympanic membrane due to the increase of reflected sound pressure. This augmentation occurs in a narrow frequency area near the maximum resonance frequency and reaches 6 dB (SPL). These experimental data correlate well with clinical investigations in patients with middle ear effusion before and after operation and in patients performing the Valsalva manoeuvre.

Psychoacoustical methods were used to study the phenomena involved in the detected of brief intensity changes within a noise burst. In subjects with normal hearing time intervals between 5 and 100 ms are noticed for the detection depending on the amount of intensity change. The value for a just noticeable difference varies with age and in pathological states. Possible peripheral and central processes of this sort of time resolution ability of the hearing organ are outlined.

The primary auditory "cortex" field L, of the Guinea fowl is a three layer tonotopically organized structure. Isofrequency planes as shown with the 2-deoxyglucose (2DG) method cut across these layers and with their second dimension extend in rostro-caudal direction. The input layer L2 exhibits "spontaneous" labeling due to high spontaneous activity of input terminals and units throughout the hearing range. The labeling is stronger locally along a rostro-caudal isofrequency contour of L2 after tone or narrow band FM stimulation. With tone stimuli the layers L1 and L3 are labeled within an isofrequency plane except for the rostral half of the field whereas frequency modulated tones do label these two layers throughout the corresponding isofrequency plane. FM stimuli in addition lead to a reduction of spontaneous labeling in frequency planes adjacent to those which are covered by the stimuli. Since these effects correlate with known inhibitory effects of such stimuli it is argued that the 2 DG method can identify the suppression of activity of neurons in suitable structures.

Fast cochlear adaptation, expressed as percent inhibition of the summed action potential, is studied from the guinea pig cochlea responses to click trains, ramps, and steps in both directions. The transition time function of adaptation to constant click trains does not depend on click strength, but rather on click interval. On the background of steady state adaptation, click steps produce only transient changes of the adaptive state, opposite to step direction. Compared to constant train stimulation, adaptation is enhanced by descending click ramps, and diminished or reversed (near threshold) by ascending ramps.

As a measure of age-related changes in the most peripheral neural part of the auditory pathway, the compound action potential of the guinea pig was analyzed. In addition to a marked threshold elevation, there was a significantly lower potential amplitude in old animals. By contrast, the latency of the compound action potential was unchanged. In view of the fact that the relative amplitude increase in the intensity range tested was the same in old as in young animals, the implication is that the auditory-nerve neurons that are still excited do not exhibit functional deterioration with aging.

The responses of 682 single-units in the inferior colliculus (IC) of 13 mustached bats (Pteronotus parnellii parnellii) were measured using pure tones (CF), frequency modulations (FM) and pairs of CF-FM signals mimicking the species' biosonar signal, which are stimuli known to be essential to the responses of CF/CF and FM-FM facilitation neurons in auditory cortex. Units were arbitrarily classified into 'reference frequency' (RF), 'FM2' and 'Non-echolocation' (NE) categories according to the relationship of their best frequencies (BF) to the biosonar signal frequencies. RF units have high Q10dB values and are tuned to the reference frequency of each bat, which ranged between 60.73 and 62.73 kHz. FM2 units had BF's between 50 and 60 kHz, while NE units had BF's outside the ranges of the RF and FM2 classes. PST histograms of the responses revealed discharge patterns such as 'onset', 'onset-bursting' (most common), 'on-off', 'tonic-on','pauser', and 'chopper'. Changes in discharge patterns usually resulted from changes in the frequency and/or intensity of the stimuli, most often involving a change from onset-bursting to on-off. Different patterns were also elicited by CF and FM stimuli. Frequency characteristics and thresholds to CF and FM stimuli were measured. RF neurons were very sharply tuned with Q10dB's ranging from 50-360. Most (92%) also responded to FM2 stimuli, but 78% were significantly more sensitive (greater than 5 dB) to CF stimuli, and only 3% had significantly lower thresholds to FM2. The best initial frequency for FM2 sweeps in RF units was 65.35 +/- 2.138 kHz (n = 118), well above the natural frequency of the 2nd harmonic. FM2 and NE units were indistinguishable from each other, but were quite different from RF units: 41% of these two classes had lower thresholds to CF, 49% were about equally sensitive, and 10% had lower thresholds to FM. For FM2 units, mean best initial frequency for FM was 60.94 kHz +/- 3.162 kHz (n = 114), which is closely matched to the 2nd harmonic in the biosonar signal. Very few units (5) responded only to FM signals, i.e., were FM-specialized. The characteristics of spike-count functions were determined in 587 units. The vast majority (79%) of RF units (n = 228) were nonmonotonic, and about 22% had upper-thresholds.(ABSTRACT TRUNCATED AT 400 WORDS)

The binaural summation of the simultaneous contra- and ipsilateral acoustic stapedius reflexes was examined in 20 normal-hearing patients. In these patients, the effect of summation was most pronounced with subthreshold intensities. A contralateral reflex was increased by ipsilateral intensities 8 db below threshold. A reflex could also be elicited by binaural intensities which were contra- and ipsilaterally 4 db below threshold. As a result of our studies, we recommend a revision of the definition of a positive Metz-recruitment. Because of possible binaural summation effects, the absolute value of the contralateral stapedius reflex threshold should not exceed 105 db HL in spite of possible sensorineural hearing loss.

Human cortical evoked potentials were monitored with scalp electrodes as an indicator of the ability to resolve brief changes in an auditory signal. For a brief period in the middle of a noise pulse its intensity was increased or decreased. The magnitude and duration of this change was varied to establish (1) the threshold for the cortical evoked potential and (2) the effect on the evoked response (amplitude, latency) in the suprathreshold region. To evoke a stimulus-specific potential pattern, durations of about 16 ms were required for intensity changes of +3 dB. With an intensity step of +9 dB, the threshold duration was reduced to 4-6 ms. A brief increase in intensity was more associated with distinctly lower thresholds and larger response amplitudes than an equivalent reduction in intensity, duration being equal. These results confirm the critical durations found in psychoacoustic studies that offer valuable evidence as to the ability to resolve brief changes in an auditory signal.

This review presents recent findings on the micromechanics of the basilar membrane. Active processes are essential for basilar membrane motion. It may be that contractile proteins within the outer hair cells play an important role for this amplification. The coding of acoustic information within the auditory nerve depends on spectral analysis (place information) as well as on the time structure of the stimulus. This latter time analysis seems to play a major role.

A method was developed to record sterotactically from the cat Superior Olivary Complex (SOC) using glass micropipettes. Sound stimulation was given through a closed system that permitted independent variation of interaural time (delta time) and intensity (delta int) differences. The most common binaural units found (n = 34) were ipsilateral excitatory, contralateral inhibitory (EI1), cells of the Lateral Superior Olive (LSO). Some Medial Superior Olive (MSO) cells and presumed MSO ascending afferents were found but, as noted by other authors, we found it difficult to obtain single unit recordings from this nucleus. The LSO EI cells were mostly sensitive to higher frequencies and showed Peristimulus Time Histograms (PSTHs) consisting of a sharp "On" response followed by a plateau when stimulated with Best Frequency (BF) tone bursts or noise bursts. This "On" response was sensitive to delta time and delta int such that ipsilateral time lead or intensity increase resulted in a stronger response. The response reached a minimum around zero delta time or delta int. No sharp peaks or dips were seen in the physiological range needed for localization, instead the response increased with increasing ipsilateral lead or intensity to the maximum values tested (2048 microseconds delta time, 30 dB delta int). In the physiological range the delta time and delta int response were complementary (both increasing response as ipsilaterality was increased). Provided enough sound energy in the unit's sensitive region was present, the same delta time curves were produced when BF tone bursts, masked tone bursts, "sharp onset" tone bursts or noise bursts were used. Changing the delta time of the carrier of the tone burst alone had no effect (except for one cell with a BF of 560 Hz), only the relative time of arrival of the stimulus envelope seemed to be important. In contrast to these LSO EI cells MSO-type units showed EI or EE predominantly low frequency phase-locked responses. When stimulated with interaurally phase shifted (delta pha) BF tones the unit response was a cyclic function of delta pha. Some cells (all that were tested, n = 6 including the 560 Hz LSO EI cell) showed these cyclic responses when stimulated with noise bursts or non-BF tones. However, these "characteristic delays" were not necessarily in the physiological range, i.e. we could find no evidence that these units were responding to delta time/delta pha values corresponding to a particular sound source direction.(ABSTRACT TRUNCATED AT 400 WORDS)

For clinical purpose it seems appropriate to emphasize especially P6 among the auditory evoked responses (AER). The latency of this positive wave after approximately 6 ms shows a close correlation of the sound intensity: approximately 9.5 ms at the hearing threshold, approximately 5.8 ms at 100 dB CHL (click hearing level). The different forms of hearing disorders always reveal typical latency patterns. Thus, middle ear hearing loss can be distinguished form inner ear hearing loss, and among sensory lesions those of moderate hearing loss exhibit another pattern than those of severe hearing loss. In the same way among neural disorders two types can be separated from each other, probably caused by different ways of genesis. Thus, ERA (electric response audiometry) becomes an objective pendant to the suprathreshold tests and an integrated part of clinical audiometry.

Test series with both continuous and intermittent sound exposure to guinea pig ears yielded an area within the coordinates load frequency and load level in which a dose principle is valid more or less exactly. Exceeding the upper (level) borderline of this area provokes a damage of the organ of Corti nearly independent of the load dose. Sound levels of such order of magnitude mainly occur at sound impulses. However, to estimate the hair-cell damaging effect of a given sound impulse one needs its time or frequency function in addition to the peak level. A first order approximation seems to be possible by means of a 1/3-octave band level analysis.

Responses of single neurones in the inferior colliculus of anesthetized adult cats and kittens were studied using best-frequency stimuli of varying interaural intensity differences (IID). Two broad classes of neurone, distinguished by the predominant type of input from each ear, were examined. One class of cells received predominantly excitatory input from each er (EE cells). The other class were excited by monaural stimulation of the contralateral ear and showed no response to monaural stimulation of the ipsilateral ear, but inhibition of the excitatory response by simultaneous ipsilateral stimulation (EI cells). Fourteen of the 18 adult EI cells showed marked changes in discharge rate with variation in IID. Adult EI cells showed low response variability and were insensitive to changes in average binaural intensity. In all cases of IID sensitivity, the onset component of the response was less sensitive to IID than the sustained component. Eight out of ten EE cells were insensitive to IID over the range tested. Cells of high best-frequency in kittens younger than 28 days showed irregular changes in discharge rate with variation in IID and wide response variability. Some low-frequency EI cells in young kittens showed sensitivity to IID, but it is unlikely that these could be involved in sound localization as their frequency response was inappropriate. Many cells in kittens aged 31-40 days showed monotonic, adult-like IID functions, but the response variability of these cells remained higher than that of adult cat neurones. These data provide evidence for a developmental change of binaural interaction in the cat.

We have examined clinically and experimentally the masking effects of white noise in registering brainstem evoked potentials and determining the Jewett-wave V. We studied input-output functions as well as latency periods of evoked potentials with masking of non-stimulated contralateral ears in 18 children aged 5-14 years. When differences of 50 dB or more were found between stimulation and masking, the Jewett-wave V could be partially suppressed. Other changes observed included alterations in potential and phase, as well as shifts in the latency period of the potentials. The clinical importance of the measurements determined indicates that findings may be used in examining patients with unilateral sensory hearing impairments to formulate possible differential diagnoses.

Single fibre recordings were performed from the auditory nerve of the caiman, Caiman crocodilus. All neurones were spontaneously active (1-80 imp/s). Clicks evoked multiple peaks in the post stimulus time histogram spaced at 1/CF. At high intensities irregularities were observed. The latencies of the first peak observable were intensity-dependent and related to CF. The number of peaks was correlated with tuning properties of the fibre. Frequency threshold curves were asymmetrical, with low frequency slopes less steep than high frequency slopes. Q10 dB was between 1.5 and 7 with best tuning at high CF. CF ranged from 30 Hz to 2.8 kHz, lowest thresholds down to 5 dB SPL. Intensity functions were nonmonotonic. In isointensity contours the best frequency shifted downwards with increasing stimulus level. At highest levels a response dip was observed above CF. Phase locking, two tone suppression and excitability by combination tones were observed. In comparison to the mammalian cochlea similarities and differences were found.

Contradictory histological findings in patients with deafness following mumps led us to conduct electrophysiological investigations. Promontory testing (PT) and measurement of cochlear microphonics (CM) enabled us to distinguish between neural and sensory deafness. On the basis of a careful history and serological tests in 19 cases of unilateral deafness we found that the hearing loss was probably caused by mumps. In all patients except one auditory sensations could be obtained by electric stimulation of the acoustic nerve whereas no CM were detectable even with strong stimuli of 100 dB tonepips. In view of the electrophysiological findings, doubt is cast on the neural genesis of deafness following mumps as assumed by Lehnhardt (1962).

Twenty ears of normal-hearing subjects are investigated as to the influence of highpass filtering on latency, amplitude, and shape of auditory evoked brain stem potentials. For this purpose, three different Bessel-filters (steepness 24 dB/octave) with lower cut-off frequencies at 100, 200, and 300 Hz (3-dB down points) and an upper cut-off frequency at 3 kHz are used. Spectral composition of brain stem potentials is analyzed by digital filtering based on Fast Fourier Transformation. Results show decreasing latency and amplitude of the negative wave between Jewett V and VI with increasing lower cut-off frequency. With higher edge frequencies we find attenuation of wave V relative to wave IV amplitudes. For that reason we must assume that an essential part of brain stem activity is located below 300 Hz. In our experience moderate highpass filtering seems to be useful in neurological cases to eliminate low frequency components of the signal. In that way potentials I -- V are easy to be identified and interpeak latencies can be determined without any problems. For objective threshold determination, however, brain stem potentials should be derived preferably with broadband filter settings to improve correlation of tone audiometric hearing loss (at about 3 kHz) and brain stem response threshold. A filter set with different lower cut-off frequencies has proved to be really useful in routine work. However, it must by taken into account that highpass filtering means an alteration of the original response in any case.

A successful cochlear implant demands a functioning auditory nerve. A subjective and qualitative recording can be obtained by promontory testing (PT) whereas cochlear microphonics (CM) give information about the status of the hair-cells in the inner ear. The results of both tests together show different patterns: in sensory deafness in which a cochlear implant is indicated, no CM and no compound action potentials (CAP) can be obtained, whereas the patient reports hearing sensations (PT positive) in response to promontory testing. Deafness caused by lesions close to the second neurone of the auditory pathways can be localized by preserved CM and CAP, but there is no response to promontory testing. A ganglionic deafness ie. of the first neurone can be distinguished by preserved CM, absent CAP and a negative PT. The combined results of electrocochleography and promontory testing help in deciding whether a cochlear implant is indicated, and in localising the origin of the deafness, eg. neural or sensorineural. The possible results are illustrated by examples.

In unanesthetized guinea pigs, thalamic (CGM), and cortical (auditory I) neurons were recorded simultaneously. Nine of 69 neuron pairs showed a positive cross-correlation of their spontaneous activities, with increased discharge probability of the cortical neuron beginning 2--5 ms after the discharge of the CGM-neuron. The individual neurons of such pairs had an identical CF and the same spectral responsiveness. The responses of cortical neurons to pure tones were much more phasic than those of the corresponding CGM-neurons. Thalamic neurons could be driven up to much higher AM- and FM-modulation frequencies (100 Hz) than cortical neurons, which usually ceased to follow AM-frequencies above 20 Hz. Stronger or weaker suppression of tonic response components in cortical and thalamic neurons and the lower AM-range of cortical neurons is related to stronger or weaker intracortical and intrathalamic inhibition respectively. Response characteristics to FM-stimuli are similar to those of AM-stimuli. All CGM and cortical neurons responded to a variety of natural calls of the same or of other species. Responses of CGM-cells represented more components of a call than cortical cells even if the two cells were synaptically connected. In cortical cells, repetitive elements of a call were not represented if the repetition rate was too high. High modulation frequencies within a call, such as those of the fundamental frequency, could still be separated in the response of some CGM-neurons, but never in those of cortical neurons. Both CGM and cortical cells responded essentially to transients (amplitude or frequency modulations) within a call, if spectral components of such elements were within the spectral sensitivity of the cell. Spectral components outside the spectral sensitivity range could result in suppression of spontaneous discharge rate. Responses of cortical and CGM-cells, and thus the representation of call elements by neuronal responses, varied with the intensity of a call. It is suggested that, at higher levels of the auditory system, essential information about the temporal features of complex sounds may be represented by neural responses to transients in various spectral regions.

Single-cell recordings from the anesthetized gerbil revealed that neurons in the ventral cochlear nucleus, the most peripheral nucleus of the central auditory system, differentially encode a functionally relevant acoustic feature--amplitude modulation. Onset units show the strongest phase--locked responses to amplitude-modulated sounds, followed in order by chopper, primarylike-with-notch and primarylike units. All these neurons show enhanced responses relative to auditory-nerve fibers which provide their ascending inputs. This enhancement occurs over a 90 dB range of sound levels.

Single neuron responses to sinusoidally amplitude modulated (SAM) signals were studied in the inferior colliculus of the horseshoe bat, Rhinolophus rouxi. 57% of the neurons responded to SAM stimuli with periodical discharges synchronized to the modulation cycle. The proportion of cells driven by amplitude modulated signals was independent of the best frequency of the neurons. Best modulation frequencies were at or below 100 Hz in about 70% of the neurons. Synchronized activity could be elicited by modulation frequencies up to 400 Hz. Best SAM responses were observed at stimulus intensities 10 dB above threshold. Generally the BMF of a neuron did not change with intensity. The BMF decreased with decreasing modulation depth of the amplitude modulation. A trend for a topographical organization of neurons according to best modulation frequencies was detected. The results did not reveal any significant specialization of the bat's auditory system for coding of amplitude modulations as compared to other mammals.