Masking Of Tones Research Articles

The effects of preceding sound on psychoacoustic tuning curves measured in simultaneous and forward masking

The medial olivocochlear reflex (MOCR) decreases the gain of the cochlear active process in response to sound. We have used psychoacoustic techniques to show behavioral effects of gain reduction, which could be consistent with the MOCR. We have used paradigms understood to measure frequency selectivity and the input/output function at the level of the cochlea using stimuli (masker and signal) that should be too short to evoke the MOCR. A precursor sound is then presented before these stimuli to evoke the MOCR. Our most recent studies have used forward masking, to avoid the complicating effects of suppression. The current study was designed to examine the effects of suppression, by comparing the effects of a precursor on frequency selectivity measured using forward masking and simultaneous masking. Psychoacoustic tuning curves were measured using simultaneous and forward masking, with and without a precursor. This allowed us to measure the change in tuning with and without the presence of suppression. Broadband precursors and tonal precursors at masker frequencies were measured because previous studies have shown broadening with broadband precursors and sharpening when tonal maskers are the precursors. Results will be discussed in the context of current understanding of the MOCR.

Intensity discrimination and neural representation of a masked tone in the presence of three types of masking release.

Hearing ability is usually evaluated by assessing the lowest detectable intensity of a target sound, commonly referred to as a detection threshold. Detection thresholds of a masked signal are dependent on various auditory cues, such as the comodulation of the masking noise, interaural differences in phase, and temporal context. However, considering that communication in everyday life happens at sound intensities well above the detection threshold, the relevance of these cues for communication in complex acoustical environments is unclear. Here, we investigated the effect of three cues on the perception and neural representation of a signal in noise at supra-threshold levels. First, we measured the decrease in detection thresholds produced by three cues, referred to as masking release. Then, we measured just-noticeable difference in intensity (intensity JND) to quantify the perception of the target signal at supra-threshold levels. Lastly, we recorded late auditory evoked potentials (LAEPs) with electroencephalography (EEG) as a physiological correlate of the target signal in noise at supra-threshold levels. The results showed that the overall masking release can be up to around 20 dB with a combination of these three cues. At the same supra-threshold levels, intensity JND was modulated by the masking release and differed across conditions. The estimated perception of the target signal in noise was enhanced by auditory cues accordingly, however, it did not differ across conditions when the target tone level was above 70 dB SPL. For the LAEPs, the P2 component was more closely linked to the masked threshold and the intensity discrimination than the N1 component. The results indicate that masking release affects the intensity discrimination of a masked target tone at supra-threshold levels, especially when the physical signal-to-noise is low, but plays a less significant role at high signal-to-noise ratios.

Spatial Release from Masking for Tones and Noises in a Soundfield under Conditions Where Targets and Maskers Are Stationary or Moving.

Stationary visual targets often become far more salient when they move against an otherwise static background–the so-called “pop out” effect. In two experiments conducted over loudspeakers, we tested for a similar pop-out effect in the auditory domain. Tone-in-noise and noise-in-noise detection thresholds were measured using a 2-up, 1-down adaptive procedure under conditions where target and masker(s) were presented from the same or different locations and when the target was stationary or moved via amplitude-panning. In the first experiment, target tones of 0.5 kHz and 4 kHz were tested, maskers (2–4, depending on the condition) were independent Gaussian noises, and all stimuli were 500-ms duration. In the second experiment, a single pink noise masker (0.3–12 kHz) was presented with a single target at one of four bandwidths (0.3–0.6 kHz, 3–6 kHz, 6–12 kHz, 0.3–12 kHz) under conditions where target and masker were presented from the same or different locations and where the target moved or not. The results of both experiments failed to show a decrease in detection thresholds resulting from movement of the target.

The increase in the degree of neural forward masking of cochlea following salicylate application

BackgroundHigh doses of salicylate are known to reduce cochlear response amplitude and raise threshold. However, its effect on the cochlear forward masking, reflecting temporal resolution, is still unclear. MethodsThe neural forward masking of cochlea was evaluated using double-tone stimulation. The first tone burst (5ms) was named the “masker” and the second tone burst (5 ms) was named the “probe”. The frequency and intensity of the masker and probe were equal, and the masker-probe interval varied from 2 to 32 ms. The reduction (%) of the probe-evoked cochlear compound action potential caused by the addition of the masker tone was used to represent cochlear forward masking. The data obtained before and 2 h following the injection of sodium salicylate (250 mg/kg) were compared. ResultsThe neural forward masking of cochlea in the normal rats increased as the masker-probe interval decreased. At 16 kHz, for example, it increased from ~5% to 32ms masker-probe interval to ~85% at 2ms masker-probe interval. Two hours post salicylate injection, the neural forward masking was significantly enhanced except at 32 ms masker-probe interval. Interestingly, this enhancement was only observed in the limited frequency range of 16–30 kHz. DiscussionThe enhancement of forward masking of cochlea following salicylate administration may reflect defective neurotransmitter release. This frequency-dependent injury in the cochlea may lead to the development of central plasticity observed after salicylate administration, likely through the increase in central gain, leading to perceptual consequences.

The role of the medial olivocochlear reflex in psychophysical masking and intensity resolution in humans: a review.

This review addresses the putative role of the medial olivocochlear (MOC) reflex in psychophysical masking and intensity resolution in humans. A framework for interpreting psychophysical results in terms of the expected influence of the MOC reflex is introduced. This framework is used to review the effects of a precursor or contralateral acoustic stimulation on 1) simultaneous masking of brief tones, 2) behavioral estimates of cochlear gain and frequency resolution in forward masking, 3) the buildup and decay of forward masking, and 4) measures of intensity resolution. Support, or lack thereof, for a role of the MOC reflex in psychophysical perception is discussed in terms of studies on estimates of MOC strength from otoacoustic emissions and the effects of resection of the olivocochlear bundle in patients with vestibular neurectomy. Novel, innovative approaches are needed to resolve the dissatisfying conclusion that current results are unable to definitively confirm or refute the role of the MOC reflex in masking and intensity resolution.

Threshold of octave masking as a tool to explain cochlear nonlinearity

Background and Aim: The threshold of octave masking test has been used to assess the growth rate of aural harmonics, the intercept point helped differentiate between normal-hearing individuals and sensorineural hearing loss due to noise exposure. With fewer literatures that have been documented, there is a need to explore this test procedure, and hence the purpose of this research is to evaluate the utility of the threshold of octave masking (TOM) procedure in understanding the frequency selectivity and non-linear function of cochlea. Methods: A total of 10 adults (20 ears) were considered for the test. The TOM test procedure was performed on the subjects where the subjects had to identify the presence of a maskee tone (1 kHz) in the presence of a masker tone (500 Hz) across 5 dB increment of masker tone until the subjects uncomfortable level. A line graph was drawn, extrapolated to identify the point of intercept, which is the threshold of octave masking. Results: Results reveal that 17 ears did not have a linear growth but had a 10 to 20 dB gap after a particular maskee level. The intercept point of the initial two extreme points was relatively more than the intercept point of the extreme points at higher intensities. Conclusion: Results from the present study have thrown light on the fact that TOM can be used as a test to measure the frequency selectivity along with the tests of psychophysical tuning curves, notched noise method, non-simultaneous masking, and other non-peripheral masking phenomena. Keywords: Threshold of octave masking; active mechanism; passive mechanism; nonlinearity;frequency selectivity; psychophysical tuning curves

Correlations between cochlear pathophysiology and behavioral measures of temporal and spatial processing in noise exposed macaques

Noise-induced hearing loss (NIHL) is known to have significant consequences for temporal, spectral, and spatial resolution. However, much remains to be discovered about their underlying pathophysiology. This report extends the recent development of a nonhuman primate model of NIHL to explore its consequences for hearing in noisy environments, and its correlations with the underlying cochlear pathology. Ten macaques (seven with normal-hearing, three with NIHL) were used in studies of masked tone detection in which the temporal or spatial properties of the masker were varied to assess metrics of temporal and spatial processing. Normal-hearing (NH) macaques showed lower tone detection thresholds for sinusoidally amplitude modulated (SAM) broadband noise maskers relative to unmodulated maskers (modulation masking release, MMR). Tone detection thresholds were lowest at low noise modulation frequencies, and increased as modulation frequency increased, until they matched threshold in unmodulated noise. NH macaques also showed lower tone detection thresholds for spatially separated tone and noise relative to co-localized tone and noise (spatial release from masking, SRM). Noise exposure caused permanent threshold shifts that were verified behaviorally and audiologically. In hearing-impaired (HI) macaques, MMR was reduced at tone frequencies above that of the noise exposure. HI macaques also showed degraded SRM, with no SRM observed across all tested tone frequencies. Deficits in MMR correlated with audiometric threshold changes, outer hair cell loss, and synapse loss, while the differences in SRM did not correlate with audiometric changes, or any measure of cochlear pathophysiology. This difference in anatomical-behavioral correlations suggests that while many behavioral deficits may arise from cochlear pathology, only some are predictable from the frequency place of damage in the cochlea.

Masking of short tones in noise: Evidence for envelope-based, rather than energy-based detection.

The "temporal effect" in simultaneous masking may be characterized by better probe detection thresholds for a short, tonal probe presented at the temporal center of a masker compared to at the onset of a masker. Energy-based models of masking have been used to interpret the temporal effect as evidence that the gain of the auditory system decreases during acoustic stimulation. This study shows that masking from temporal-envelope fluctuations of a precursor or from a temporal gap between stimuli violates the assumptions of energy-based models and complicates the interpretation of temporal effects in terms of a reduction in gain. Detection thresholds were measured for a 6-ms, 4000-Hz probe preceded by a narrowband precursor and presented 2-, 197-, or 392-ms after the onset of a narrowband masker. The delay between the precursor offset and masker onset ranged from -2 to 250 ms. Probe thresholds were elevated in the presence of precursors with fluctuating compared to flattened temporal envelopes and when a temporal gap was inserted between the precursor and masker. The results suggest that the interpretation and design of temporal-effect studies should consider the masking effects of temporal-envelope fluctuations. These findings are consistent with speech-perception experiments that show masking from temporal-envelope fluctuations.

Identifying cues for tone-in-noise detection using decision variable correlation in the budgerigar (Melopsittacus undulatus).

Previous studies evaluated cues for masked tone detection using reproducible noise waveforms. Human results founded on this approach suggest that tone detection is based on combined energy and envelope (ENV) cues, but detection cues in nonhuman species are less clear. Decision variable correlation (DVC) was used to evaluate tone-in-noise detection cues in the budgerigar, an avian species with human-like behavioral sensitivity to many complex sounds. DVC quantifies a model's ability to predict trial-by-trial variance in behavioral responses. Budgerigars were behaviorally conditioned to detect 500-Hz tones in wideband (WB; 100-3000 Hz) and narrowband (NB; 452-552 Hz) noise. Behavioral responses were obtained using a single-interval, two-alternative discrimination task and two-down, one-up adaptive tracking procedures. Tone-detection thresholds in WB noise were higher than human thresholds, putatively due to broader peripheral frequency tuning, whereas NB thresholds were within ∼1 dB of human results. Budgerigar average hit and false-alarm rates across noise waveforms were consistent, highly correlated across subjects, and correlated to human results. Trial-by-trial behavioral results in NB noise were best explained by a model combining energy and ENV cues. In contrast, WB results were better predicted by ENV-based or multiple-channel energy detector models. These results suggest that budgerigars and humans use similar cues for tone-in-noise detection.

Amplitude modulation detection and modulation masking in school-age children and adults.

Two experiments were performed to better understand on- and off-frequency modulation masking in normal-hearing school-age children and adults. Experiment 1 estimated thresholds for detecting 16-, 64- or 256-Hz sinusoidal amplitude modulation (AM) imposed on a 4300-Hz pure tone. Thresholds tended to improve with age, with larger developmental effects for 64- and 256-Hz AM than 16-Hz AM. Detection of 16-Hz AM was also measured with a 1000-Hz off-frequency masker tone carrying 16-Hz AM. Off-frequency modulation masking was larger for younger than older children and adults when the masker was gated with the target, but not when the masker was continuous. Experiment 2 measured detection of 16- or 64-Hz sinusoidal AM carried on a bandpass noise with and without additional on-frequency masker AM. Children and adults demonstrated modulation masking with similar tuning to modulation rate. Rate-dependent age effects for AM detection on a pure-tone carrier are consistent with maturation of temporal resolution, an effect that may be obscured by modulation masking for noise carriers. Children were more susceptible than adults to off-frequency modulation masking for gated stimuli, consistent with maturation in the ability to listen selectively in frequency, but the children were not more susceptible to on-frequency modulation masking than adults.

Implementing an efferent signal into an auditory pathway model for tone-in-noise detection

Simultaneous tone-in-noise detection has been studied extensively, but typically without consideration of the medial olivocochlear (MOC) efferents. We are testing hypotheses for masked detection using a central auditory model with a signal from midbrain to MOC. Masked tones are encoded in the rate profile of band-enhanced (BE) inferior colliculus (IC) neurons, which are excited by a range of modulation frequencies. Peripheral responses to noise are characterized by large fluctuations, an effective stimulus for BE IC neurons. In contrast, peripheral channels tuned near the tone have smaller fluctuations: addition of the tone flattens the signal envelope and also pushes the inner hair cell (IHC) transduction nonlinearity further into saturation. Excitatory projections to MOC from noise-driven BE IC cells would decrease cochlear gain, reducing IHC saturation, and resulting in larger fluctuations and IC rates. In contrast, tone-plus-noise-driven channels would reduce MOC excitation, resulting in relatively higher cochlear gain, more saturation, and ultimately lower IC rates. Thus, the descending signal from IC BE cells to MOC is hypothesized to enhance contrast in the IC rate profile. Because efferents have slow dynamics, timing is an important factor. Therefore, we focus on model sensitivity to masked tones of different durations for comparison to psychophysical trends.

Masking of short tones in noise: Evidence for envelope-based, rather than energy-based detection

A short tone added to a longer simultaneous masker may be detected by observing an increase in overall acoustic energy. This detection scheme predicts probe thresholds to be independent of the masker’s temporal envelope. A recent study [Jennings et al., J. Assoc. Res. Oto. 19, 717–727 (2018)] revealed that probe thresholds were 10 dB higher for maskers with flattened compared to fluctuating envelopes, suggesting an envelope-based detection strategy. This study test the hypothesis that probe thresholds are proportional to envelope power by measuring detection thresholds for a 4-kHz, 6-ms probe in one of three temporal positions within a 400-ms masker in normal-hearing listeners. The narrow-band, low-fluctuating noise masker was preceded by flattened or fluctuating noise precursors. The precursor’s offset was delayed from the masker’s onset by -2, 0, 10, 25, 100, or 250 ms. Probe thresholds were positively correlated with envelope power (R-squared = 0.75), consistent with masking from precursor envelope fluctuations and from fluctuations introduced by precursor and masker ramps. These findings suggest that future modeling efforts for short probes presented in longer maskers should consider a decision variable based on envelope fluctuations.

Pitch perception of concurrent high-frequency complex tones

Accurate pitch perception is possible for harmonic complex tones with fundamental frequencies (F0s) in the musical range (e.g., 1.4 kHz) but with all harmonics beyond the putative limits of phase locking. However, it is unknown whether pitch perception in more complex scenarios, such as with concurrent complex tones, is possible using these stimuli. To address this question, we measured (1) F0 difference limens (F0DLs) and (2) target-to-masker ratios (TMRs) required to detect a fixed F0 difference in a mixture of complex tones with low F0s (∼280 Hz) or high F0s (∼1400 Hz). The target tones were filtered to ensure that in the high-F0 case, only harmonics beyond the limits of phase locking were present. Pitch perception was poorer for isolated high-F0 tones than for isolated low-F0 tones and adding a masker complex tone with a geometrically centered F0 impaired performance for both high-F0 and low-F0 tones. The TMRs required to achieve good performance in the presence of two complex tone maskers were higher for high-F0 tones than for low-F0 tones. The results should help determine whether different mechanisms underlie the perception of combinations of complex tones at low and high frequencies. [Work supported by Grants NIH R01 DC005216 and NSF NRT-UtB1734815.]Accurate pitch perception is possible for harmonic complex tones with fundamental frequencies (F0s) in the musical range (e.g., 1.4 kHz) but with all harmonics beyond the putative limits of phase locking. However, it is unknown whether pitch perception in more complex scenarios, such as with concurrent complex tones, is possible using these stimuli. To address this question, we measured (1) F0 difference limens (F0DLs) and (2) target-to-masker ratios (TMRs) required to detect a fixed F0 difference in a mixture of complex tones with low F0s (∼280 Hz) or high F0s (∼1400 Hz). The target tones were filtered to ensure that in the high-F0 case, only harmonics beyond the limits of phase locking were present. Pitch perception was poorer for isolated high-F0 tones than for isolated low-F0 tones and adding a masker complex tone with a geometrically centered F0 impaired performance for both high-F0 and low-F0 tones. The TMRs required to achieve good performance in the presence of two complex tone maskers were higher...

Speech Perception with Spectrally Non-overlapping Maskers as Measure of Spectral Resolution in Cochlear Implant Users.

Poor spectral resolution contributes to the difficulties experienced by cochlear implant (CI) users when listening to speech in noise. However, correlations between measures of spectral resolution and speech perception in noise have not always been found to be robust. It may be that the relationship between spectral resolution and speech perception in noise becomes clearer in conditions where the speech and noise are not spectrally matched, so that improved spectral resolution can assist in separating the speech from the masker. To test this prediction, speech intelligibility was measured with noise or tone maskers that were presented either in the same spectral channels as the speech or in interleaved spectral channels. Spectral resolution was estimated via a spectral ripple discrimination task. Results from vocoder simulations in normal-hearing listeners showed increasing differences in speech intelligibility between spectrally overlapped and interleaved maskers as well as improved spectral ripple discrimination with increasing spectral resolution. However, no clear differences were observed in CI users between performance with spectrally interleaved and overlapped maskers, or between tone and noise maskers. The results suggest that spectral resolution in current CIs is too poor to take advantage of the spectral separation produced by spectrally interleaved speech and maskers. Overall, the spectrally interleaved and tonal maskers produce a much larger difference in performance between normal-hearing listeners and CI users than do traditional speech-in-noise measures, and thus provide a more sensitive test of speech perception abilities for current and future implantable devices.

Backward masking of tones and speech in people who do and do not stutter

PurposeThere is evidence of an auditory-perceptual component of stuttering, and backward masking (BM) is a task to explore that role. Prior research reported poorer thresholds for BM tones in a group of children who persisted in stuttering compared to those for a group that did not persist. This study examined BM for adults who stutter for tones and for speech, which tests a phonetic aspect of hearing. MethodEight persons who stutter (PWS) were closely matched with eight controls (PNS) in terms of phonological abilities, verbal span tasks, age, sex and non-verbal intelligence. These participants were examined for their ability to recognize vowel-consonant (VC) speech syllables and tones in BM paradigm with 0 ms and 300 ms masker to signal onset conditions. ResultsPWS showed significantly poorer performance for speech syllable recognition in quiet and in conditions with masking noise. The pattern of speech errors was similar in both groups, but the PWS produced more errors. A significant condition by group interaction in backward masking for tones was attributed to higher masked thresholds in PWS than in PNS in the 0 ms delay condition for BM for tones. ConclusionThis was the first study to examine BM for speech in PWS. Results provide support for a small auditory-perceptual deficit for speech understanding in adults who stutter that was revealed in the absence of a lexical context. The speech results are explained in terms of possible indistinct phoneme boundaries in PWS and the effects of vowel context in speech recognition.

Masking of an auditory behaviour reveals how male mosquitoes use distortion to detect females.

The mating behaviour of many mosquito species is mediated essentially by sound: males follow and mate with a female mid-flight by detecting and tracking the whine of her flight-tones. The stereotypical rapid frequency modulation (RFM) male behaviour, initiated in response to the detection of the female's flight-tones, has provided a means of investigating these auditory mechanisms while males are free-flying. Mosquitoes hear with their antennae, which vibrate to near-field acoustic excitation. The antennae generate nonlinear vibrations (distortion products, DPs) at frequencies that are equal to the difference between the two simultaneously presented tones, e.g. the male and female flight-tones, which are detected by mechanoreceptors in the auditory Johnston's organ (JO) at the base of the antenna. Recent studies indicated the male mosquito's JO is tuned not to the female flight-tone, but to the frequency difference between the male and female flight-tones. To test the hypothesis that mosquitoes detect this frequency difference, Culex quinquefasciatus males were presented simultaneously with a female flight-tone and a masking tone, which should suppress the male's RFM response to sound. The free-flight behavioural and in vivo electrophysiological experiments revealed that acoustic masking suppresses the RFM response to the female's flight-tones by attenuating the DPs generated in the nonlinear vibration of the antennae. These findings provide direct evidence in support of the hypothesis that male mosquitoes detect females when both are in flight through difference tones generated in the vibrations of their antennae owing to the interaction between their own flight-tones and those of a female.

Masking release by combined spatial and masker-fluctuation effects in the open sound field.

In a complex auditory scene, signals of interest can be distinguished from masking sounds by differences in source location [spatial release from masking (SRM)] and by differences between masker-alone and masker-plus-signal envelopes. This study investigated interactions between those factors in release of masking of 700-Hz tones in an open sound field. Signal and masker sources were colocated in front of the listener, or the signal source was shifted 90° to the side. In Experiment 1, the masker contained a 25-Hz-wide on-signal band plus flanking bands having envelopes that were either mutually uncorrelated or were comodulated. Comodulation masking release (CMR) was largely independent of signal location at a higher masker sound level, but at a lower level CMR was reduced for the lateral signal location. In Experiment 2, a brief signal was positioned at the envelope maximum (peak) or minimum (dip) of a 50-Hz-wide on-signal masker. Masking was released in dip more than in peak conditions only for the 90° signal. Overall, open-field SRM was greater in magnitude than binaural masking release reported in comparable closed-field studies, and envelope-related release was somewhat weaker. Mutual enhancement of masking release by spatial and envelope-related effects tended to increase with increasing masker level.

Frequency selectivity in macaque monkeys measured using a notched-noise method

The auditory system is thought to process complex sounds through overlapping bandpass filters. Frequency selectivity as estimated by auditory filters has been well quantified in humans and other mammalian species using behavioral and physiological methodologies, but little work has been done to examine frequency selectivity in nonhuman primates. In particular, knowledge of macaque frequency selectivity would help address the recent controversy over the sharpness of cochlear tuning in humans relative to other animal species. The purpose of our study was to investigate the frequency selectivity of macaque monkeys using a notched-noise paradigm. Four macaques were trained to detect tones in noises that were spectrally notched symmetrically and asymmetrically around the tone frequency. Masked tone thresholds decreased with increasing notch width. Auditory filter shapes were estimated using a rounded exponential function. Macaque auditory filters were symmetric at low noise levels and broader and more asymmetric at higher noise levels with broader low-frequency and steeper high-frequency tails. Macaque filter bandwidths (BW3dB) increased with increasing center frequency, similar to humans and other species. Estimates of equivalent rectangular bandwidth (ERB) and filter quality factor (QERB) suggest macaque filters are broader than human filters. These data shed further light on frequency selectivity across species and serve as a baseline for studies of neuronal frequency selectivity and frequency selectivity in subjects with hearing loss.

Manifestation of peripherial coding in the effect of increasing loudness and enhanced discrimination of the intensity of tone bursts before and after tone burst noise

To find the possible reasons for the midlevel elevation of the Weber fraction in intensity discrimination of a tone burst, a comparison was performed for the complementary distributions of spike activity of an ensemble of space nerves, such as the distribution of time instants when spikes occur, the distribution of interspike intervals, and the autocorrelation function. The distribution properties were detected in a poststimulus histogram, an interspike interval histogram, and an autocorrelation histogram—all obtained from the reaction of an ensemble of model space nerves in response to an auditory noise burst–useful tone burst complex. Two configurations were used: in the first, the peak amplitude of the tone burst was varied and the noise amplitude was fixed; in the other, the tone burst amplitude was fixed and the noise amplitude was varied. Noise could precede or follow the tone burst. The noise and tone burst durations, as well as the interval between them, was 4 kHz and corresponded to the characteristic frequencies of the model space nerves. The profiles of all the mentioned histograms had two maxima. The values and the positions of the maxima in the poststimulus histogram corresponded to the amplitudes and mutual time position of the noise and the tone burst. The maximum that occurred in response to the tone burst action could be a basis for the formation of the loudness of the latter (explicit loudness). However, the positions of the maxima in the other two histograms did not depend on the positions of tone bursts and noise in the combinations. The first maximum fell in short intervals and united intervals corresponding to the noise and tone burst durations. The second maximum fell in intervals corresponding to a tone burst delay with respect to noise, and its value was proportional to the noise amplitude or tone burst amplitude that was smaller in the complex. An increase in tone burst or noise amplitudes was caused by nonlinear variations in the two maxima and the ratio between them. The size of the first maximum in the of interspike interval distribution could be the basis for the formation of the loudness of the masked tone burst (implicit loudness), and the size of the second maximum, for the formation of intensity in the periodicity pitch of the complex. The auditory effect of the midlevel enhancement of tone burst loudness could be the result of variations in the implicit tone burst loudness caused by variations in tone-burst or noise intensity. The reason for the enhancement of the Weber fraction could be competitive interaction between such subjective qualities as explicit and implicit tone-burst loudness and the intensity of the periodicity pitch of the complex.

Predicting performance across different psychoacoustic tasks

How likely is it that listeners who are superior on one aural attribute are also superior on a second aural attribute? The ability of listeners was measured on two psychoacoustic tasks: (1) detection of tones in noise and (2) detection of amplitude modulation for masked tone complexes. We tested nine listeners (4 M and 5 F) with clinically normal hearing and an age range of 18-21 years using a transformed up-down method with trial-by-trial feedback, and averaged over three measurements. First we determined absolute thresholds for 500-ms tones. Then, using three levels of tones spanning a 30 dB range, we determined both masked tone detection (F = 1, 2, 4, 8 kHz) and masked three-tone discrimination (same center frequencies) with modulation frequencies of Fm = 3, 30, 300 Hz. We discuss how to analyze the data obtained to determine whether a listener’s performance on a given task can be used to predict performance on other tasks.