Dennis P. Phillips

Acquired word deafness, and the temporal grain of sound representation in the primary auditory cortex.

This paper explores the nature of the processing disorder which underlies the speech discrimination deficit in the syndrome of acquired word deafness following from pathology to the primary auditory cortex. A critical examination of the evidence on this disorder revealed the following. First, the most profound forms of the condition are expressed not only in an isolation of the cerebral linguistic processor from auditory input, but in a failure of even the perceptual elaboration of the relevant sounds. Second, in agreement with earlier studies, we conclude that the perceptual dimension disturbed in word deafness is a temporal one. We argue, however, that it is not a generalized disorder of auditory temporal processing, but one which is largely restricted to the processing of sounds with temporal content in the milliseconds to tens-of-milliseconds time frame. The perceptual elaboration of sounds with temporal content outside that range, in either direction, may survive the disorder. Third, we present neurophysiological evidence that the primary auditory cortex has a special role in the representation of auditory events in that time frame, but not in the representation of auditory events with temporal grains outside that range.

Word recognition in continuous and interrupted broadband noise by young normal-hearing, older normal-hearing, and presbyacusic listeners

Objective: Word recognition performance in continuous and interrupted broadband noise was examined in young normal‐hearing (YNH), older normal‐hearing (ONH), and presbyacusic (older hearing‐impaired [OHI]) listeners. Design: Participants (N = 36) were presented with identical Northwestern University Auditory Test No. 6 stimuli at 30 dB sensation level re their respective speech reception thresholds. The speech stimuli were presented in quiet and in both competing noise conditions with signal to noise ratios(S/Ns) of 10, 5, 0, ‐5, ‐10, ‐15, and ‐20 dB. Results: In general performance was superior in quiet, improved with increasing S/N, and was greater in the interrupted broadband noise than in the continuous broadband noise. Significant main effects of group and S/N were found in both competing noises (p < 0.0001). Post hoc pairwise comparisons revealed all groups performed differently, with superior performance being displayed by the YNH group followed by the ONH and OHI groups, respectively (p < 0.05). A significant group by S/N interaction was observed in only the interrupted noise condition (p= 0.019). The degree of change in word recognition performance as a function of S/N was greatest in the OHI group followed by the ONH group and the YNH group. Conclusions: Group effects observed in the interrupted noise would imply that the two older groups of listeners had an auditory temporal deficit relative to the YNH listeners. The paradigm reveals the patency of the temporal processes that are responsible for the perceptual advantage (i.e., a release from masking) a listener has in interrupted competing stimulus.

Neural representation of sound amplitude in the auditory cortex: effects of noise masking

Single auditory cortical neurons express their sensitivity to the amplitude of a preferred-frequency tone pulse as either a monotonic, saturating intensity profile or as a non-monotonic, bell-shaped intensity function. In the presence of continuous, wideband noise masking, the tone intensity profile is displaced toward higher tone levels. The magnitude of the tone threshold adjustments brought about by increments in noise level very closely match the elevations in noise amplitude. The mechanisms underlying the threshold adjustments likely include neural adaptation. This is because the tone threshold shifts seen in the spike count data are paralleled by spike latency data, and because recovery of tonal sensitivity following noise offset proceeds in a negatively-accelerating fashion. In some instances, the slope of the masked tone intensity profile is greater than that for unmasked tones. For masked tone levels evoking submaximal responses, this has the consequence that cortical responses to masked tones are somewhat more salient than those for unmasked tones of comparable suprathreshold level. These observations bolster our understanding of the psychophysics of noise-masking in normal listeners, and they provide a partial explanation of the difficulty shown by patients with temporal lobe lesions in discriminating signals in noise.

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.

Representation of acoustic events in the primary auditory cortex

One approach to the problem of specifying the contribution of the primary auditory cortex to auditory perception has been based on single-neuron recording techniques in animals. These experiments measure the response rates of individual neural elements to parametric variations in 1 or more stimulus dimensions. The patterns of response rates and response failures revealed by these manipulations are quantitative descriptions of the form and fidelity of the cortexs representation of those stimulus dimensions. This strategy has been used to advantage in studies of the cortical representation of the spectral content of auditory events, the spatial location of a sound, and the time structure of sounds. The data constitute new links between neural coding and behavioral performance in normal and impaired listeners.

Coding of interaural time differences of transients in auditory cortex of rattus norvegicus implications for the evolution of mammalian sound localization

We obtained quantitative evidence on the coding of interaural time differences (ITDs) of click stimuli by 40 single neurons in the auditory cortex of anesthetized albino rats. Most of the neurons (31/40) received an excitatory input from the contralateral ear, and an inhibitory input from the ipsilateral ear (EI cells). These neurons expressed their sensitivity to ITDs in a sigmoidal relation between spike count and ITD, with maximal responses associated with contralateral-leading ITDs. The mean ITD dynamic range was 590 microseconds. The dynamic ranges typically encompassed at least part of the behaviorally-relevant range (about +/- 130 microseconds). Variations in ITD from 130 microseconds favoring one ear to 130 microseconds favoring the other ear caused spike response rate changes, on average, of 29.5%. These data are similar to those previously presented for the central auditory systems of larger mammals, whose auditory localization acuity is significantly better than that of the rat. We argue, therefore, that the sound localization mechanisms based on transient ITDs have not evolved in a fashion that covaries with interaural distance, and that there exists a mismatch between the ITDs the rat will encounter in the free field, and the ITDs which are encoded by its nervous system. This may be one reason why sound localization acuity has a roughly inverse relation to interaural distance.

Psychophysical evidence for adaptation of central auditory processors for interaural differences in time and level

Human listeners were studied for their ability to lateralize single target tones of each of two frequencies relative to midline clicks. They did so before and after exposure to adaptor tones of the same frequencies. The adaptor tones were strongly lateralized, and in opposite directions for each frequency, by either an interaural time difference (ITD, Experiment 1) or interaural level difference (ILD, Experiment 2). Following adaptation, psychometric functions for ITD (Exp. 1) and ILD (Exp. 2) were obtained for target tones for the two frequencies separately. These were found to be shifted in the direction of the fatigued side. In the case of ILD, this was in the absence of a shift in monaural sensitivity sufficient to account for the effect. For both ITD and ILD studies, shifts in perceived laterality were induced in opposite directions at two frequencies concurrently. This effect was induced with only seconds of intermittent exposure to the adaptor tones. The fact that it could be induced at two frequencies in opposite directions at the same time, suggests (a), that these data constitute new psychophysical evidence for the frequency specificity of ITD and ILD coding in the human brain, and (b), that the effect was not due to the introduction of some response bias at the decision level of perceptual judgement. The data are interpreted in terms of a two- or three-channel opponent process model.

Separate Mechanisms Control Spike Numbers and Inter-Spike Intervals in Transient Responses of Cat Auditory-Cortex Neurons

In the anesthetized cat, some cortical auditory neurons discharge a train of up to 5 spikes in response to the onset of a characteristic frequency tone pulse. This report provides the first description of the inter-spike intervals (ISIs) in these responses. The ISIs were typically close to 2.0 ms in length, and, as indexed by the standard deviation of the interval length, were very regular. Except at threshold levels of stimulation, mean ISIs were relatively insensitive to both tone amplitude and repetition rate. This was true even over ranges of those variables that exerted dramatic effects on spike numbers and first spike latency. These data suggest that the relative timing of discharges within the spike burst is controlled by a mechanism which is separable from that which determines the number of spikes in them. The brevity of the ISIs suggest that they may be a means of enhancing the salience of the transient response against a background of spontaneous discharges.

A perceptual architecture for sound lateralization in man

There are two general neurophysiological models of sound lateralization mechanisms which may be active in man. Both of the models are derived from studies in animals (one in barn owls, and one in mammals), and both have displayed some weakness in generalizability. One model advocates a population of neurons narrowly tuned to different interaural disparity values across the behaviorally relevant range, so that the cue value, and therefore the source azimuth, is represented by which neurons of the array are activated by the stimulus. The second model posits the existence of only two neural channels, each broadly tuned to interaural cue values favoring one acoustic hemifield, so that, especially for sources near the midline, cue value and therefore source azimuth is encoded by the relative activation of the two neural populations. The present article reviews three recent psychophysical studies, each using selective adaptation paradigms to probe sound lateralization mechanisms based on interaural disparities in normal human listeners. These experiments provided evidence on the frequency-specificity of interaural disparity coding and revealed its sensitivity to recent stimulus history. The data from those studies, however, also help distinguish the two lateralization models, and favor a perceptual architecture for sound lateralization in man based on the activity of two, hemifield-tuned azimuthal channels.

Correlations among within-channel and between-channel auditory gap-detection thresholds in normal listeners

We obtained data on within-channel and between-channel auditory temporal gap-detection acuity in the normal population. Ninety-five normal listeners were tested for gap-detection thresholds, for conditions in which the gap was bounded by spectrally identical, and by spectrally different, acoustic markers. Separate thresholds were obtained with the use of an adaptive tracking method, for gaps delimited by narrowband noise bursts centred on 1.0 kHz, noise bursts centred on 4.0 kHz, and for gaps bounded by a leading marker of 4.0 kHz noise and a trailing marker of 1.0 kHz noise. Gap thresholds were lowest for silent periods bounded by identical markers—‘within-channel’ stimuli. Gap thresholds were significantly longer for the between-channel stimulus—silent periods bounded by unidentical markers (p < 0.0001). Thresholds for the two within-channel tasks were highly correlated (R = 0.76). Thresholds for the between-channel stimulus were weakly correlated with thresholds for the within-channel stimuli (1.0 kHz, R = 0.39; and 4.0 kHz, R = 0.46). The relatively poor predictability of between-channel thresholds from the within-channel thresholds is new evidence on the separability of the mechanisms that mediate performance of the two tasks. The data confirm that the acuity difference for the tasks, which has previously been demonstrated in only small numbers of highly trained listeners, extends to a population of untrained listeners. The acuity of the between-channel mechanism may be relevant to the formation of voice-onset time-category boundaries in speech perception.