Frequency discrimination in the monkey

This study evaluated frequency discrimination ability in 11 monkeys over an extended period of time using a repeating-standard procedure and the method of constant stimuli. The intersubject variability of the difference limens for frequency (delta F) was large, as reported by other investigators, but similar in magnitude to the variability of the difference limens for intensity (delta I) from three of the same subjects in an intensity discrimination experiment. Continued training generally resulted in a rapid decrease in delta F's, followed by a longer-term, slower decrease. For one subject delta F's slowly decreased throughout a 190-week time period. This long-term training effect was specific to frequency discrimination; a similar effect was not observed for the same subject tested in an intensity discrimination experiment. Finally, delta F's from the well-trained monkeys of this study were larger than monkey delta F's from this laboratory reported in an earlier study, and than human delta F's. An anatomical explanation for the human/monkey delta F magnitude difference is explored.     

Perceptual learning in frequency discrimination

This study was concerned with the effects of training on the frequency discrimination ability of human listeners. Frequency discrimination at 200 Hz was tested before and after training. Four groups of listeners received training in four different frequency regions, 200, 360, 2500, and 6000 Hz. It was found that training at 200, 360, and 2500 Hz all provided comparable improvement in discrimination performance at 200 Hz whereas training at 6000 Hz provided less improvement. This result is consistent with the idea that frequency discrimination and pitch perception are mediated by different processes at high (greater than 5000 Hz) and low (less than 5000 Hz) frequencies.     

Frequency discrimination of tones presented in filtered noise

Previous research (Emmerich et al., 1983) in which tones were presented in the center of the notches in band-reject noise backgrounds suggests that information from frequency regions remote from the nominal signal frequency is useful in frequency discrimination. The present work extends the earlier findings by presenting tones on either side of a notch so that only one (or the other) tail of the excitation patterns of the tones would fall into the notch. In addition, tones were presented in high-pass noise, low-pass noise, and various combinations of the two. The results again indicate that remote information affects frequency discrimination, and they are also consistent with the hypothesis that the low-frequency tail of the excitation pattern is more useful for frequency discrimination than is the high-frequency tail.     

Frequency discrimination in forward and backward masking.

Frequency difference limens for pure tones preceded by a forward masker or followed by a backward masker were obtained across a wide range of signal levels. Relkin and Doucet [Hear. Res. 55, 215-222 (1991)] have shown that at a masker-signal delay of 100 ms, the thresholds of high-SR (spontaneous rate) auditory-nerve fibers are recovered, while the low-SR fiber thresholds are not. Therefore, forward-masked frequency discrimination potentially offers a method to investigate the role of low-SR fibers in the coding of frequency. It has been shown that when an intense forward masker is presented 100 ms before a pure-tone signal, intensity difference limens are elevated for mid-level signals [Zeng et al., Hear. Res. 55, 223-230 (1991)]. However, Plack and Viemeister [J. Acoust. Soc. Am. 92, 3097-3101 (1992)] have shown that a similar elevation in the intensity difference limen is obtained under conditions of backward masking, where selective adaptation of the auditory neurons would not be expected to occur. A condition of backward-masked frequency discrimination was therefore included to investigate the role of interference resulting from adding additional stimuli to a discrimination task. For signals at 1000 and 6000 Hz, there was no effect of a forward masker upon frequency difference limens. For the backward-masked conditions, an elevation of the frequency difference limen was observed at all signal levels, demonstrating that the effects of forward and backward maskers upon frequency discrimination are dissimilar and suggesting that cognitive effects are present in backward-masked discrimination tasks.(ABSTRACT TRUNCATED AT 250 WORDS)     

Frequency and intensity discrimination in humans and monkeys

Frequency and intensity DLs were compared in humans and monkeys using a repeating standard "yes-no" procedure in which subjects reported frequency increments, frequency decrements, intensity increments, or intensity decrements in an ongoing train of 1.0-kHz tone bursts. There was only one experimental condition (intensity increments) in which monkey DLs (1.5-2.0 dB) overlapped those of humans (1.0-1.8 dB). For discrimination of both increments and decrements in frequency, monkey DLs (16-33 Hz) were approximately seven times larger than those of humans (2.4-4.8 Hz), and for discrimination of intensity decrements, monkey DLs (4.4-7.0 dB) were very unstable and larger than those of humans (1.0-1.8 dB). For intensity increment discrimination, humans and monkeys also exhibited similar DLs as SL was varied. However, for frequency increment discrimination, best DLs for humans occurred at a high (50 dB) SL, whereas best DLs for monkeys occurred at a moderate (30 dB) SL. Results are discussed in terms of various neural mechanisms that might be differentially engaged by humans and monkeys in performing these tasks; for example, different amounts of temporal versus rate coding in frequency discrimination, and different mechanisms for monitoring rate decreases in intensity discrimination. The implications of these data for using monkeys as models of human speech sound discrimination are also discussed.     

Frequency discrimination for pulsed versus modulated tones

Estimates of frequency discrimination for pulsed modulated tones were obtained by 11 observers at 350, 500, 1000, 4000, and 8000 Hz. At low frequencies, frequency DL's are larger for modulated than for pulsed tones; at 8000 Hz the contrary was found. Frequency DL's (difference limens) determined by different methods and procedures differed by a factor up to four; extreme individual frequency DL's, however, by a factor up to 27.     

Frequency and intensity discrimination in human infants and adults

Frequency and intensity DLs were measured in 26 human infants (ages 7-9 months) and six young adults using a repeating standard "yes-no" operant headturning technique and an adaptive staircase (tracking) psychophysical procedure. Subjects were visually reinforced for responding to frequency increments, frequency decrements, intensity increments, or intensity decrements in an ongoing train of 1.0-kHz tone bursts, and stimulus control was monitored using randomly interleaved probe and catch trials. Infants were easily conditioned to respond to both increments and decrements in frequency, and DLs ranged from 11-29 Hz, while adult DLs ranged from 3-5 Hz. Infants also easily discriminated intensity increments, and DLs ranged from 3-12 dB, while adult DLs ranged from 1-2 dB. No infants successfully discriminated intensity decrements, although adults experienced no difficulty with this task and produced DLs similar to those for increments. The apparent inability of infants to discriminate intensity decrements suggests that the infant CNS may not be well adapted to monitor rate decreases in populations of peripheral auditory neurons.     

Specificity of perceptual learning in a frequency discrimination task

On a variety of visual tasks, improvement in perceptual discrimination with practice (perceptual learning) has been found to be specific to features of the training stimulus, including retinal location. This specificity has been interpreted as evidence that the learning reflects changes in neuronal tuning at relatively early processing stages. The aim of the present study was to examine the frequency specificity of human auditory perceptual learning in a frequency discrimination task. Difference limens for frequency (DLFs) were determined at 5 and 8 kHz, using a three-alternative forced choice method, for two groups of eight subjects before and after extensive training at one or the other frequency. Both groups showed substantial improvement at the training frequency, and much of this improvement generalized to the nontrained frequency. However, a small but statistically significant component of the improvement was specific to the training frequency. Whether this specificity reflects changes in neural frequency tuning or attentional changes remains unclear.     

Frequency discrimination in the mammalian cochlea: theory versus experiment

A three-dimensional hydroelastic model for the motion in the cochlea is analyzed for the case of a pure-tone forcing. It is shown to agree well with experiment, including moderate intensity tuning curves and the frequency map, for a variety of mammals. In doing this, the parameters that are needed for each animal are geometric; thus the theory is easy to apply. The analysis also indicates that the fluid viscosity is the dominant dissipation mechanism, at least for moderate to high frequencies.     

Frequency discrimination of complex tones with overlapping and non-overlapping harmonics

These experiments address the following issues. (1) When two complex tones contain different harmonics, do the differences in timbre between them impair the ability to discriminate the pitches of the tones? (2) When two complex tones have only a single component in common, and that component is the most discriminable component in each tone, is the frequency discrimination of the component affected by differences in residue pitch between the two tones? (3) How good is the pitch discrimination of complex tones with no common components when each tone contains multiple harmonics, so as to avoid ambiguity of pitch? (4) Is the pitch discrimination of complex tones with common harmonics impaired by shifting the component frequencies to nonharmonic values? In all experiments, frequency difference limens (DLCs) were measured for multiple-component complex tones, using an adaptive two-interval, two-alternative, forced-choice task. Three highly trained subjects were used. The main conclusions are as follows. (1) When two tones have the first six harmonics in common, DLCs are larger when the upper harmonics are different than when the upper harmonics are in common or are absent. It appears that differences in timbre impair DLCs. (2) Discrimination of the frequency of a single common partial in two complex tones is worse when the two tones have different residue pitches than when they have the same residue pitch. (3) DLCs for complex tones with no common harmonics are generally larger than those for complex tones with common harmonics. For the former, large individual differences occur, probably because subjects are affected differently by differences in timbre. (4) DLCs for harmonic complex tones are smaller than DLCs for complex tones in which the components are mistuned from harmonic values. This can probably be attributed to the less distinct residue pitch of the inharmonic complexes, rather than to reduced discriminability of partials. Overall, the results support the idea that DLCs for complex tones with common harmonics depend on residue pitch comparisons, rather than on comparisons of the pitches of partials.     

Frequency discrimination in quiet and in noise for signals with triangular spectral envelopes

The just-noticeable-difference in frequency (jndf) for complex signals with triangular spectral envelopes is found to depend on the envelope slope. For shallow slopes (less than 140 dB/oct), jndf increases with decreasing slope. Addition of noise also impairs frequency discrimination within a region of about 20 dB above masked threshold. This is found for both maskers used: a wideband noise and a narrow-band masker which is below the signal in frequency. When wideband noise is used, frequency discrimination of complex signals with shallow slopes deteriorates more rapidly with decreasing signal-to-noise ratio than it does when the signals have steep spectral slopes.     

Frequency discrimination near the spectral edge of simultaneous and forward maskers

The effects of the presence of an amplitude discontinuity in the spectrum of a noise masker on frequency discrimination performance were examined. First, detection thresholds as a function of masker level were obtained for pure-tone signals masked by either simultaneous or forward white and low-pass maskers. Then frequency discrimination thresholds were obtained using four masker levels that were chosen to yield predetermined masked thresholds, with signal levels corresponding to each of three sensation levels above these masked thresholds. The principal results indicate that frequency discrimination is poorer in simultaneous low-pass noise than in simultaneous white noise, and that this difference in performance increases with increasing sensation level and with increasing masker level. These results are inconsistent with an explanation based on the pitches generated at spectral edges ("edge pitch"), pitch shifts, or disruption of phase-locking information, but are generally consistent with an explanation based on lateral suppression. It is proposed that a release from suppression may occur in filtered noise backgrounds at high noise levels and at high sensation levels. The reduced suppression may result in poorer frequency discrimination due, in part, to reduced signal detectability.     

Frequency discrimination under conditions of comodulation masking release (L)

Masked detection thresholds can often be improved by introducing coherent masker amplitude modulation across frequency, a phenomenon referred to as comodulation masking release (CMR). While CMR can be large for detection, it is smaller for supra-threshold tasks, such as intensity discrimination. In this experiment, frequency discrimination for a 1000-Hz tone near threshold was found to be poorer in an amplitude-modulated than a steady bandpass noise. These results parallel previous findings for intensity discrimination. Although this study examined the relatively simple task of frequency discrimination, the results may have implications for more complex tasks, such as speech recognition in fluctuating noise.