Psychoacoustics publications

Frequency selectivity was evaluated under two conditions designed to assess the influence of a “precursor” stimulus on auditory filter bandwidths. The standard condition consisted of a short masker, immediately followed by a short signal. The precursor condition was identical except a 100-ms sinusoid at the signal frequency (i.e., the precursor) was presented before the masker. The standard and precursor conditions were compared for measurements of psychophysical tuning curves (PTCs), and notched noise tuning characteristics. Estimates of frequency selectivity were significantly broader in the precursor condition. In the second experiment, PTCs in the standard and precursor conditions were simulated to evaluate the influence of the precursor on PTC bandwidth. The model was designed to account for the influence of additivity of masking between the masker and precursor. Model simulations were able to qualitatively account for the perceptual data when outer hair cell gain of the model was reduced in the precursor condition. These findings suggest that the precursor may have reduced cochlear gain, in addition to producing additivity of masking. This reduction in gain may be mediated by the medial olivocochlear reflex.

The physiology of the medial olivocochlear reflex suggests that a sufficiently long stimulus (>100 ms) may reduce cochlear gain and result in broadened frequency selectivity. The current study attempted to avoid gain reduction by using short maskers (20 ms) to measure psychophysical tuning curves (PTCs) and notched-noise tuning characteristics, with a 4-kHz signal. The influence of off-frequency listening on PTCs was evaluated using two types of background noise. Iso-level curves were derived using an estimate of the cochlear input/output (I/O) function, which was obtained using an off-frequency masker as a linear reference. The influence of masker duration on PTCs was assessed using a model that assumed long maskers (>20 ms) evoked gain reduction. The results suggested that the off-frequency masker was a valid linear reference when deriving I/O functions and that off-frequency listening may have occurred in auditory filters apical to the signal place. The iso-level curves from this growth-of-masking study were consistent with those from a temporal-masking-curve study by Eustaquio-Martin and Lopez-Poveda [J. Assoc. Res. Otolaryngol. 12, 281–299. (2011)], suggesting that either approach may be used to derive iso-level curves. Finally, model simulations suggested that masker duration may not influence estimates of frequency selectivity.

Objectives: This study aimed to (1) investigate the relationship between the acoustic change complex (ACC) and perceptual measures of frequency and intensity discrimination, and gap detection; and (2) examine the effects of acoustic change on the amplitudes and latencies of the ACC. Design: Psychophysical thresholds for frequency and intensity discrimination and gap detection, as well as ACCs elicited by stimuli containing increments in frequency, or intensity or gaps, were recorded from the same group of subjects. The magnitude of the acoustic change was systematically varied for the ACC recording. Study sample: Twenty-six adults with normal hearing, ranging in age between 19 and 39 years. Results: Electrophysiological and psychophysical measures for frequency and intensity discrimination were significantly correlated. Electrophysiological thresholds were comparable to psychophysical thresholds for intensity discrimination but were higher than psychophysical thresholds for gap detection and frequency discrimination. Increasing the magnitude of acoustic change increased the ACC amplitude but did not show consistent effects across acoustic dimensions for ACC latency. Conclusions: The ACC can be used as an objective index of auditory discrimination in frequency and intensity. The ACC amplitude is a better indicator for auditory processing than the ACC latency.

Spatial release from masking refers to a benefit for speech understanding. It occurs when a target talker and a masker talker are spatially separated. In those cases, speech intelligibility for target speech is typically higher than when both talkers are at the same location. In cochlear implant listeners, spatial release from masking is much reduced or absent compared with normal hearing listeners. Perhaps this reduced spatial release occurs because cochlear implant listeners cannot effectively attend to spatial cues. Three experiments examined factors that may interfere with deploying spatial attention to a target talker masked by another talker. To simulate cochlear implant listening, stimuli were vocoded with two unique features. First, we used 50-Hz low-pass filtered speech envelopes and noise carriers, strongly reducing the possibility of temporal pitch cues; second, co-modulation was imposed on target and masker utterances to enhance perceptual fusion between the two sources. Stimuli were presented over headphones. Experiments 1 and 2 presented high-fidelity spatial cues with unprocessed and vocoded speech. Experiment 3 maintained faithful long-term average interaural level differences but presented scrambled interaural time differences with vocoded speech. Results show a robust spatial release from masking in Experiments 1 and 2, and a greatly reduced spatial release in Experiment 3. Faithful long-term average interaural level differences were insufficient for producing spatial release from masking. This suggests that appropriate interaural time differences are necessary for restoring spatial release from masking, at least for a situation where there are few viable alternative segregation cues.

It is well known that damage to the peripheral auditory system causes deficits in tone detection as well as pitch and loudness perception across a wide range of frequencies. However, the extent to which to which the auditory cortex plays a critical role in these basic aspects of spectral processing, especially with regard to speech, music, and environmental sound perception, remains unclear. Recent experiments indicate that primary auditory cortex is necessary for the normally-high perceptual acuity exhibited by humans in pure-tone frequency discrimination. The present study assessed whether the auditory cortex plays a similar role in the intensity domain and contrasted its contribution to sensory versus discriminative aspects of intensity processing. We measured intensity thresholds for pure-tone detection and pure-tone loudness discrimination in a population of healthy adults and a middle-aged man with complete or near-complete lesions of the auditory cortex bilaterally. Detection thresholds in his left and right ears were 16 and 7 dB HL, respectively, within clinically-defined normal limits. In contrast, the intensity threshold for monaural loudness discrimination at 1 kHz was 6.5 ± 2.1 dB in the left ear and 6.5 ± 1.9 dB in the right ear at 40 dB sensation level, well above the means of the control population (left ear: 1.6 ± 0.22 dB; right ear: 1.7 ± 0.19 dB). The results indicate that auditory cortex lowers just-noticeable differences for loudness discrimination by approximately 5 dB but is not necessary for tone detection in quiet. Previous human and Old-world monkey experiments employing lesion-effect, neurophysiology, and neuroimaging methods to investigate the role of auditory cortex in intensity processing are reviewed.

Frequency selectivity is a fundamental cochlear property. Recent studies using otoacoustic emissions and psychophysical forward masking suggest that frequency selectivity is sharper in human than in common laboratory species. This has been disputed based on reports using compound action potentials (CAPs), which reflect activity in the auditory nerve and can be measured in humans. Comparative data of CAPs, obtained with a variety of simultaneous masking protocols, have been interpreted to indicate similarity of frequency tuning across mammals and even birds. Unfortunately, there are several issues with the available CAP measurements which hamper a straightforward comparison across species. We investigate sharpness of CAP tuning in cat and chinchilla using a forward masking notched-noise paradigm--which is less confounded by cochlear nonlinearities than simultaneous masking paradigms and similar to what was used in the psychophysical study reporting sharper tuning in humans. Our parametric study, using different probe frequencies and notch widths, shows relationships consistent with those of auditory nerve fibers (ANFs). The sharpness of tuning, quantified by Q(10) factors, is negatively correlated with probe level and increases with probe frequency, but the Q(10) values are generally lower than the average trend for ANFs. Like the single fiber data, tuning for CAPs is sharper in cat than in chinchilla, but the two species are similar in the dependence of tuning on probe frequency and in the relationship between tuning in ANFs and CAP. Growth-of-maskability functions show slopes <1 indicating that with increasing probe level the probe is more susceptible to cochlear compression than the masker. The results support the use of forward-masked CAPs as an alternative measure to estimate ANF tuning and to compare frequency tuning across species.

Objectives: : To measure spatial acuity on a right-left discrimination task in 2-to-3-year-old children who use a unilateral cochlear implant (UCI) or bilateral cochlear implants (BICIs); to test the hypothesis that BICI users perform significantly better when they use two CIs than when using a single CI, and that they perform better than the children in the UCI group; to determine how well children with CIs perform compared with children who have normal acoustic hearing (NH); to determine the effect of intensity roving on spatial acuity. Design: : Three groups of children between 26 and 36 months of age participated in this study: 8 children with NH (mean age: 30.9 months), 12 children who use a UCI (mean age: 31.9 months), and 27 children who use BICIs (mean age: 30.7 months). Testing was conducted in a large sound-treated booth with loudspeakers positioned in a horizontal arc with a radius of 1.2 m. The observer-based psychophysical procedure was used to measure the children's ability to identify the hemifield containing the sound source (right versus left). Two methods were used for quantifying spatial acuity, an adaptive-tracking method and a fixed-angle method. In Experiment 1 an adaptive tracking algorithm was used to vary source angle, and the minimum audible angle (MAA), the smallest angle at which right-left discrimination performance is better than chance, was estimated. All three groups participated in Experiment 1. In Experiment 2 source angles were fixed at ±50 degrees, and performance was evaluated by computing the number of SDs above chance. Children in the UCI and BICI groups participated in Experiment 2. Results: : In Experiment 1, when stimulus intensity was roved by 8 dB, MAA thresholds were 3.3 degrees to 30.2 degrees (mean = 14.5 degrees) and 5.7 degrees to 69.6 degrees (mean = 30.9 degrees) in the NH group and in the BICI group, respectively. When the intensity level was fixed for the BICI group, performance did not improve. Within the BICI group, 5 out of 27 children obtained MAA thresholds within one SD of their peers who have NH; all five had >12 months of bilateral listening experience. In Experiment 2, BICIs provided some advantages when the intensity level was fixed. First, the BICI group outperformed the UCI group. Second, children in the BICI group who repeated the task with their 1st CI alone had statistically significantly better performance when using both devices. In addition, when intensity roving was introduced, a larger percentage of children who had 12 or more months of BICI experience continued to perform above chance than children who had <12 months of BICI experience. Taken together, the results suggest that children with BICIs have spatial acuity that is better than when using their first CI alone and than that of their peers who use UCIs. In addition, longer durations of BICI use tend to result in better performance, although this cannot be generalized to all participants. Conclusion: : This report is consistent with a growing body of evidence that spatial-hearing skills can emerge in young children who use BICIs. The observation that these skills are not concomitantly emerging in age- and experience-matched children who use UCIs suggests that BICIs provide cues that are necessary for these spatial-hearing skills that UCIs do not provide.

The relative sensitivity of human listeners to interaural level differences (ILDs) carried by the onsets, offsets, and interior portions of brief sounds was examined. Stimuli consisted of single 4000-Hz Gabor clicks (Gaussian-windowed tone bursts) or trains of 16 such clicks repeating at an interclick interval (ICI) of 2 or 5 ms. In separate conditions, ILDs favored the right ear by a constant amount for all clicks (condition RRRR) or a changing amount that was maximal at sound onset (condition R000), offset (condition 000R), both onset and offset (condition R00R), or at the temporal midpoint of the stimulus (condition 0RR0). ILD increases and decreases were implemented as linear decibel sweeps across four clicks to minimize transient distortion. Threshold ILDs were determined adaptively for each of these conditions and for single clicks. Thresholds were similar for ILDs presented near sound onset or offset (condition R000 vs 000R) but lower when ILDs were carried by both onset and offset clicks (condition R00R) than for ILDs carried by interior clicks alone (condition 0RR0). The results suggest that similar sensitivity to onset and offset ILD does not reflect uniform temporal weighting; instead, ILD sensitivity favors onsets and offsets over the interior portions of sounds.

The speech signal may be divided into spectral frequency-bands, each band containing temporal properties of the envelope and fine structure. This study measured the perceptual weights for the envelope and fine structure in each of three frequency bands for sentence materials in young normal-hearing listeners, older normal-hearing listeners, aided older hearing-impaired listeners, and spectrally matched young normal-hearing listeners. The availability of each acoustic property was independently varied through noisy signal extraction. Thus, the full speech stimulus was presented with noise used to mask six different auditory channels. Perceptual weights were determined by correlating a listener’s performance with the signal-to-noise ratio of each acoustic property on a trial-by-trial basis. Results demonstrate that temporal fine structure perceptual weights remain stable across the four listener groups. However, a different weighting typography was observed across the listener groups for envelope cues. Results suggest that spectral shaping used to preserve the audibility of the speech stimulus may alter the allocation of perceptual resources. The relative perceptual weighting of envelope cues may also change with age. Concurrent testing of sentences repeated once on a previous day demonstrated that weighting strategies for all listener groups can change, suggesting an initial stabilization period or susceptibility to auditory training.

This study investigated the ability to use cues contained within vowel and consonant segments by older listeners with normal or impaired hearing. Spectral shaping restored audibility for the hearing-impaired group. Word and sentence materials were processed to contain primarily consonants or vowels by replacing segments with low-level speech-shaped noise. The proportion of the total duration of preserved speech was varied by manipulating the amount of transitional information contained within vowel and consonant segments. Older listeners performed more poorly than young listeners on all conditions except when listening to sentences with only the vowels preserved. Results confirmed a greater contribution to intelligibility of vowel segments in sentences, but not in words, for young normal-hearing, older normal-hearing, and older hearing-impaired listeners. Older listeners received a greater benefit than young listeners from vowels presented in a sentence context. Correlation analyses among the older listeners demonstrated an association between consonant and vowel performance in isolated words but not in sentences. In addition, the use of vowel cues in sentences was relatively independent of age and auditory sensitivity when audibility is ensured. Combined, results argue that older listeners are able to use essential cues carried by vowels for sentence intelligibility.

Human listeners' sensitivity to interaural time differences (ITD) was assessed for 1000 Hz tone bursts (500 ms duration) preceded by trains of 500-ms "adapter" tone bursts (7 s total adapter duration, frequencies of 200, 665, 1000, or 1400 Hz) carrying random ITD, or by an equal-duration period of silence. Presentation of the adapter burst train reduced ITD sensitivity in a frequency-specific manner. The observed effect differs from previously described forms of location-specific psychophysical adaptation, as it was produced using a binaurally diffuse sequence of tone bursts (i.e., a location-nonspecific adapter stimulus). Results are discussed in the context of pre-binaural adaptation.

The long, rambling warble song of male budgerigars is composed of a large number of acoustically complex elements uttered in streams lasting minutes a time and accompanied by various courtship behaviors. Warble song has no obvious sequential structure or patterned repetition of elements, raising questions as to which aspects of it are perceptually salient, whether budgerigars can detect changes in natural warble streams, and to what extent these capabilities are species-specific. Using operant conditioning and a psychophysical paradigm, we examined the sensitivity of budgerigars, canaries, and zebra finches to changes in long (>6 min) natural warble sequences of a male budgerigar. All three species could detect a single insertion of pure tones, zebra finch song syllables, budgerigar contact calls, or warble elements from another budgerigar's warble. In each case, budgerigars were more sensitive to these changes than were canaries or finches. When warble elements from the ongoing warble stream were used as targets and inserted, out of order, into the natural warble stream so that the only cue available was the violation of the natural ordering of warble elements, only budgerigars performed above chance. When the experiment was repeated with all the ongoing warble stream elements presented in random order, the performance of budgerigars fell to chance. These results show species-specific advantages in budgerigars for detecting acoustic changes in natural warble sequences and indicate at least a limited sensitivity to sequential rules governing the structure of their species-specific warble songs.

Level-dependent changes in temporal envelope fluctuations in speech and related changes in speech recognition may reveal effects of basilar-membrane nonlinearities. As a result of compression in the basilar-membrane response, the "effective" magnitude of envelope fluctuations may be reduced as speech level increases from lower level (more linear) to mid-level (more compressive) regions. With further increases to a more linear region, speech envelope fluctuations may become more pronounced. To assess these effects, recognition of consonants and key words in sentences was measured as a function of speech level for younger adults with normal hearing. Consonant-vowel syllables and sentences were spectrally degraded using "noise vocoder" processing to maximize perceptual effects of changes to the speech envelope. Broadband noise at a fixed signal-to-noise ratio maintained constant audibility as speech level increased. Results revealed significant increases in scores and envelope-dependent feature transmission from 45 to 60 dB SPL and decreasing scores and feature transmission from 60 to 85 dB SPL. This quadratic pattern, with speech recognition maximized at mid levels and poorer at lower and higher levels, is consistent with a role of cochlear nonlinearities in perception of speech envelope cues.

Key points The cerebral cortex plays a critical role in perception and in learning‐induced plasticity. We show that reversibly silencing any of the main regions of auditory cortex impairs the ability of adult ferrets to localize sound, with the largest deficit seen after deactivating the primary fields. Although these animals had no trouble localizing longer sound bursts, their performance dropped considerably when auditory spatial cues were altered by occluding one ear with an earplug. In contrast to control ferrets, which recovered their localization abilities with intensive training, adaptation to an earplug was impaired following cortical inactivation, with the greatest disruption in plasticity observed after silencing higher‐level cortical areas. These findings imply regional differences in the processing of spatial information across the auditory cortex. Abstract The contribution of auditory cortex to spatial information processing was explored behaviourally in adult ferrets by reversibly deactivating different cortical areas by subdural placement of a polymer that released the GABA A agonist muscimol over a period of weeks. The spatial extent and time course of cortical inactivation were determined electrophysiologically. Muscimol‐Elvax was placed bilaterally over the anterior (AEG), middle (MEG) or posterior ectosylvian gyrus (PEG), so that different regions of the auditory cortex could be deactivated in different cases. Sound localization accuracy in the horizontal plane was assessed by measuring both the initial head orienting and approach‐to‐target responses made by the animals. Head orienting behaviour was unaffected by silencing any region of the auditory cortex, whereas the accuracy of approach‐to‐target responses to brief sounds (40 ms noise bursts) was reduced by muscimol‐Elvax but not by drug‐free implants. Modest but significant localization impairments were observed after deactivating the MEG, AEG or PEG, although the largest deficits were produced in animals in which the MEG, where the primary auditory fields are located, was silenced. We also examined experience‐induced spatial plasticity by reversibly plugging one ear. In control animals, localization accuracy for both approach‐to‐target and head orienting responses was initially impaired by monaural occlusion, but recovered with training over the next few days. Deactivating any part of the auditory cortex resulted in less complete recovery than in controls, with the largest deficits observed after silencing the higher‐level cortical areas in the AEG and PEG. Although suggesting that each region of auditory cortex contributes to spatial learning, differences in the localization deficits and degree of adaptation between groups imply a regional specialization in the processing of spatial information across the auditory cortex.

The acoustic rearing environment can alter central auditory coding properties, yet altered neural coding is seldom linked with specific deficits to adult perceptual skills. To test whether developmental hearing loss resulted in comparable changes to perception and sensory coding, we examined behavioral and neural detection thresholds for sinusoidally amplitude modulated (sAM) stimuli. Behavioral sAM detection thresholds for slow (5 Hz) modulations were significantly worse for animals reared with bilateral conductive hearing loss (CHL), as compared to controls. This difference could not be attributed to hearing thresholds, proficiency at the task, or proxies for attention. Detection thresholds across the groups did not differ for fast (100 Hz) modulations, a result paralleling that seen in humans. Neural responses to sAM stimuli were recorded in single auditory cortex neurons from separate groups of awake animals. Neurometric analyses indicated equivalent thresholds for the most sensitive neurons, but a significantly poorer detection threshold for slow modulations across the population of CHL neurons as compared to controls. The magnitude of the neural deficit matched that of the behavioral differences, suggesting that a reduction of sensory information can account for limitations to perceptual skills.

Previous cochlear implant studies using isolated electrical stimulus pulses in animal models have reported that intracochlear monopolar stimulus configurations elicit broad extents of neuronal activation within the central auditory system-much broader than the activation patterns produced by bipolar electrode pairs or acoustic tones. However, psychophysical and speech reception studies that use sustained pulse trains do not show clear performance differences for monopolar versus bipolar configurations. To test whether monopolar intracochlear stimulation can produce selective activation of the inferior colliculus, we measured activation widths along the tonotopic axis of the inferior colliculus for acoustic tones and 1,000-pulse/s electrical pulse trains in guinea pigs and cats. Electrical pulse trains were presented using an array of 6-12 stimulating electrodes distributed longitudinally on a space-filling silicone carrier positioned in the scala tympani of the cochlea. We found that for monopolar, bipolar, and acoustic stimuli, activation widths were significantly narrower for sustained responses than for the transient response to the stimulus onset. Furthermore, monopolar and bipolar stimuli elicited similar activation widths when compared at stimulus levels that produced similar peak spike rates. Surprisingly, we found that in guinea pigs, monopolar and bipolar stimuli produced narrower sustained activation than 60 dB sound pressure level acoustic tones when compared at stimulus levels that produced similar peak spike rates. Therefore, we conclude that intracochlear electrical stimulation using monopolar pulse trains can produce activation patterns that are at least as selective as bipolar or acoustic stimulation.

Large conductance, voltage‐ and Ca 2+ ‐activated K + (BK) channels in inner hair cells (IHCs) of the cochlea are essential for hearing. However, germ‐line deletion of BKα, the pore‐forming subunit KCNMA1 of the BK channel, surprisingly did not affect hearing thresholds in the first postnatal weeks, even though altered IHC membrane time constants, decreased IHC receptor potential alternating current/direct current ratio, and impaired spike timing of auditory fibers were reported in these mice. To investigate the role of IHC BK channels for central auditory processing, we generated a conditional mouse model with hair cell‐specific deletion of BKα from postnatal day 10 onward. This had an unexpected effect on temporal coding in the central auditory system: neuronal single and multiunit responses in the inferior colliculus showed higher excitability and greater precision of temporal coding that may be linked to the improved discrimination of temporally modulated sounds observed in behavioral training. The higher precision of temporal coding, however, was restricted to slower modulations of sound and reduced stimulus‐driven activity. This suggests a diminished dynamic range of stimulus coding that is expected to impair signal detection in noise. Thus, BK channels in IHCs are crucial for central coding of the temporal fine structure of sound and for detection of signals in a noisy environment.—Kurt, S., Sausbier, M., Rüttiger, L., Brandt, N., Moeller, C. K., Kindler, J., Sausbier, U., Zimmermann, U., van Straaten, H., Neuhuber, W., Engel, J., Knipper, M., Ruth, P., Schulze, H. Critical role for cochlear hair cell BK channels for coding the temporal structure and dynamic range of auditory information for central auditory processing. FASEB J. 26, 3834–3843 (2012). www.fasebj.org

Purpose To establish the range of talker variability for vowel intelligibility in clear versus conversational speech for older adults with hearing loss and to determine whether talkers who produced a clear speech benefit for young listeners with normal hearing also did so for older adults with hearing loss. Method Clear and conversational vowels in /bVd/ context produced by 41 talkers were presented in noise for identification by 40 older (ages 65–87 years) adults with sloping sensorineural hearing loss. Results Vowel intelligibility within each speaking style and the size of the clear speech benefit varied widely among talkers. The clear speech benefit was equivalent to that enjoyed by young listeners with normal hearing in an earlier study. Most talkers who had produced a clear speech benefit for young listeners with normal hearing also did so for the older listeners with hearing loss in the present study. However, effects of talker gender differed between listeners with normal hearing and listeners with hearing loss. Conclusion The clear speech vowel intelligibility benefit generated for listeners with hearing loss varied considerably among talkers. Most talkers who produced a clear speech benefit for normal-hearing listeners also produced a benefit for listeners with hearing loss.

Temporal processing declines with age may reduce the processing of concurrent vowels. For this study, listeners categorized vowel pairs varying in temporal asynchrony as one sound, two overlapping sounds, or two sounds separated by a gap. Two boundaries separating the three response categories, multiplicity and gap-identification, were measured. Compared to young and middle-aged listeners, older listeners required longer temporal offsets for multiplicity. Middle-aged and older listeners also required longer offsets for gap-identification. For older listeners, correlations with various temporal processing tasks indicated that vowel temporal-order thresholds were related to multiplicity, while age and non-speech gap-detection thresholds were related to gap-identification.

Natural sounds are characterized by complex patterns of sound intensity distributed across both frequency (spectral modulation) and time (temporal modulation). Perception of these patterns has been proposed to depend on a bank of modulation filters, each tuned to a unique combination of a spectral and a temporal modulation frequency. There is considerable physiological evidence for such combined spectrotemporal tuning. However, direct behavioral evidence is lacking. Here we examined the processing of spectrotemporal modulation behaviorally using a perceptual-learning paradigm. We trained human listeners for ∼1 h/d for 7 d to discriminate the depth of spectral (0.5 cyc/oct; 0 Hz), temporal (0 cyc/oct; 32 Hz), or upward spectrotemporal (0.5 cyc/oct; 32 Hz) modulation. Each trained group learned more on their respective trained condition than did controls who received no training. Critically, this depth-discrimination learning did not generalize to the trained stimuli of the other groups or to downward spectrotemporal (0.5 cyc/oct; −32 Hz) modulation. Learning on discrimination also led to worsening on modulation detection, but only when the same spectrotemporal modulation was used for both tasks. Thus, these influences of training were specific to the trained combination of spectral and temporal modulation frequencies, even when the trained and untrained stimuli had one modulation frequency in common. This specificity indicates that training modified circuitry that had combined spectrotemporal tuning, and therefore that circuits with such tuning can influence perception. These results are consistent with the possibility that the auditory system analyzes sounds through filters tuned to combined spectrotemporal modulation.