Abstract:Forward masking of a sinusoidal signal is determined not only by the masker’s power spectrum but also by its phase spectrum. Specifically, when the phase spectrum is such that the output of an auditory filter centred on the signal has a highly modulated (“peaked”) envelope, there is less masking than when that envelope is flat. This finding has been attributed to non-linearities, such as compression, reducing the average neural response to maskers that produce more peaked auditory filter outputs (Carlyon and D… Show more
“…SCHR+ and SCHR− complexes with equal duty cycles have equal long‐term magnitude spectra and similar acoustical envelopes (ENVs). To date, the perception of SCHR complexes has been evaluated primarily in birds (Dooling et al, 2002) and humans (Carlyon et al, 2017; Drennan et al, 2008; Kohlrausch & Sander, 1995; Oxenham & Dau, 2001, 2004), whereas neural studies have focused on small mammals (e.g., Cedolin & Delgutte, 2010; Recio, 2001). The present study in the Mongolian gerbil for the first time relates behavior and single‐unit responses to SCHR complexes at different levels of the auditory pathway in the same species in order to investigate the physiological basis of perception.…”
Section: Introductionmentioning
confidence: 99%
“…Interesting perceptual differences between SCHR stimuli challenge some of the basic premises of hearing science, such as the role of the magnitude and phase spectra of complex sounds. Consequently, SCHR complexes have played a key role in psychophysical investigations of cochlear function and neural coding, including the phase response of auditory filters (e.g., Carlyon et al, 2017; Kohlrausch & Sander, 1995; Oxenham & Dau, 2001, 2004), the effect of the phase spectrum on masking (e.g., Carlyon & Datta, 1997; Smith et al, 1986), and sensitivity to temporal fine structure (TFS; e.g., Dooling et al, 2002; Drennan et al, 2008).…”
Schroeder‐phase harmonic tone complexes have been used in physiological and psychophysical studies in several species to gain insight into cochlear function. Each pitch period of the Schroeder stimulus contains a linear frequency sweep; the duty cycle, sweep velocity, and direction are controlled by parameters of the phase spectrum. Here, responses to a range of Schroeder‐phase harmonic tone complexes were studied both behaviorally and in neural recordings from the auditory nerve and inferior colliculus of Mongolian gerbils. Gerbils were able to discriminate Schroeder‐phase harmonic tone complexes based on sweep direction, duty cycle, and/or velocity for fundamental frequencies up to 200 Hz. Temporal representation in neural responses based on the van Rossum spike‐distance metric, with time constants of either 1 ms or related to the stimulus' period, was compared with average discharge rates. Neural responses and behavioral performance were both expressed in terms of sensitivity, d', to allow direct comparisons. Our results suggest that in the auditory nerve, stimulus fine structure is represented by spike timing, whereas envelope is represented by rate. In the inferior colliculus, both temporal fine structure and envelope appear to be represented best by rate. However, correlations between neural d' values and behavioral sensitivity for sweep direction were strongest for both temporal metrics, for both auditory nerve and inferior colliculus. Furthermore, the high sensitivity observed in the inferior colliculus neural rate‐based discrimination suggests that these neurons integrate across multiple inputs arising from the auditory periphery.
“…SCHR+ and SCHR− complexes with equal duty cycles have equal long‐term magnitude spectra and similar acoustical envelopes (ENVs). To date, the perception of SCHR complexes has been evaluated primarily in birds (Dooling et al, 2002) and humans (Carlyon et al, 2017; Drennan et al, 2008; Kohlrausch & Sander, 1995; Oxenham & Dau, 2001, 2004), whereas neural studies have focused on small mammals (e.g., Cedolin & Delgutte, 2010; Recio, 2001). The present study in the Mongolian gerbil for the first time relates behavior and single‐unit responses to SCHR complexes at different levels of the auditory pathway in the same species in order to investigate the physiological basis of perception.…”
Section: Introductionmentioning
confidence: 99%
“…Interesting perceptual differences between SCHR stimuli challenge some of the basic premises of hearing science, such as the role of the magnitude and phase spectra of complex sounds. Consequently, SCHR complexes have played a key role in psychophysical investigations of cochlear function and neural coding, including the phase response of auditory filters (e.g., Carlyon et al, 2017; Kohlrausch & Sander, 1995; Oxenham & Dau, 2001, 2004), the effect of the phase spectrum on masking (e.g., Carlyon & Datta, 1997; Smith et al, 1986), and sensitivity to temporal fine structure (TFS; e.g., Dooling et al, 2002; Drennan et al, 2008).…”
Schroeder‐phase harmonic tone complexes have been used in physiological and psychophysical studies in several species to gain insight into cochlear function. Each pitch period of the Schroeder stimulus contains a linear frequency sweep; the duty cycle, sweep velocity, and direction are controlled by parameters of the phase spectrum. Here, responses to a range of Schroeder‐phase harmonic tone complexes were studied both behaviorally and in neural recordings from the auditory nerve and inferior colliculus of Mongolian gerbils. Gerbils were able to discriminate Schroeder‐phase harmonic tone complexes based on sweep direction, duty cycle, and/or velocity for fundamental frequencies up to 200 Hz. Temporal representation in neural responses based on the van Rossum spike‐distance metric, with time constants of either 1 ms or related to the stimulus' period, was compared with average discharge rates. Neural responses and behavioral performance were both expressed in terms of sensitivity, d', to allow direct comparisons. Our results suggest that in the auditory nerve, stimulus fine structure is represented by spike timing, whereas envelope is represented by rate. In the inferior colliculus, both temporal fine structure and envelope appear to be represented best by rate. However, correlations between neural d' values and behavioral sensitivity for sweep direction were strongest for both temporal metrics, for both auditory nerve and inferior colliculus. Furthermore, the high sensitivity observed in the inferior colliculus neural rate‐based discrimination suggests that these neurons integrate across multiple inputs arising from the auditory periphery.
Amplitude modulation (AM) of a masker reduces its masking on a simultaneously presented unmodulated pure-tone target, which likely involves dip listening. This study tested the idea that dip-listening efficiency may depend on stimulus context, i.e., the match in AM peakedness (AMP) between the masker and a precursor or postcursor stimulus, assuming a form of temporal pattern analysis process. Masked thresholds were measured in normal-hearing listeners using Schroeder-phase harmonic complexes as maskers and precursors or postcursors. Experiment 1 showed threshold elevation (i.e., interference) when a flat cursor preceded or followed a peaked masker, suggesting proactive and retroactive temporal pattern analysis. Threshold decline (facilitation) was observed when the masker AMP was matched to the precursor, irrespective of stimulus AMP, suggesting only proactive processing. Subsequent experiments showed that both interference and facilitation (1) remained robust when a temporal gap was inserted between masker and cursor, (2) disappeared when an F0-difference was introduced between masker and precursor, and (3) decreased when the presentation level was reduced. These results suggest an important role of envelope regularity in dip listening, especially when masker and cursor are F0-matched and, therefore, form one perceptual stream. The reported effects seem to represent a time-domain variant of comodulation masking release.
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