Size of critical band in infants, children, and adults

Masked thresholds at two signal frequencies (0.8 and 4 kHz) were obtained from listeners aged 6.5 months, 2 years, 5 years, and 20.5 years in the presence of constant spectrum level, narrowband maskers of differing bandwidths. Consistent with the classical results of Fletcher (1940), masked threshold for all age groups increased with bandwidth up to a critical width, beyond which further increases in bandwidth were ineffective in increasing threshold. These critical widths (estimates of critical band size) did not change substantially with age (critical widths for infants were no more than 50% larger than those of adults) despite substantial changes in masked thresholds with age. Thus, contrary to previous claims, changes in auditory filter width cannot account for developmental changes in masked or absolute thresholds.     

Hearing in passerine and psittacine birds: a comparative study of absolute and masked auditory thresholds

Operant conditioning and a psychophysical tracking procedure were used to measure auditory thresholds for pure tones in quiet and in noise for seven species of small birds--the budgerigar, canary, cockatiel, European starling, song sparrow, swamp sparrow, and the zebra finch. Audibility curves are roughly similar among the seven birds, with the maximum sensitivity between 2 and 5 kHz and poorer sensitivity outside this narrow region. Critical ratios (signal-to-noise ratio at masked threshold) were calculated from pure-tone thresholds in noise. Except for the budgerigar, the critical ratio functions of all birds increase at the rate of 3 dB/octave. This pattern is typical of that observed in most vertebrates. Critical ratios in the budgerigar, on the other hand, decrease gradually from 0.5 kHz to 2.8 kHz and increase dramatically above 2.8 kHz. The present research demonstrates that the critical ratio function for the budgerigar is not only different from other vertebrates but also different from other birds.     

Detection by the guinea pig of acoustic stimulation and of electrical stimulation of the brain

A threshold procedure using operant behavioral techniques with positive reinforcement was developed after initial efforts with avoidance behavioral procedures proved unsatisfactory. In the first of three experiments the operant threshold procedure was tested by determining masked auditory thresholds for trains of clicks. In a second experiment, similar techniques were used to measure thresholds for electrical stimulation of the brain. The last experiment, again an auditory problem, involved a determination of the absolute thresholds for trains of short noise bursts as a function of the time between bursts. Middle ear malfunction proved to be a more severe problem than had been anticipated on the basis of reports in the literature. The threshold procedure, however, seems to be adequate for determination of absolute or masked thresholds with auditory or electrical stimuli.     

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.     

A comparison of thresholds for 1/3-octave filtered clicks and noise bursts in infants and adults

Behavioral thresholds of 6-month-old infants and adults were determined for 1/3-octave filtered clicks and 300-msec noise bursts with center frequencies ranging from .5 to 8 kHz. For noise bursts, differences between infant and adult thresholds were largest at low frequencies and smallest at 8 kHz. For clicks, infants’ thresholds were most like adults’ at 4 kHz, and age differences increased at both lower and higher frequencies. Differences between click and noise thresholds were significantly larger for infants than for adults at .5, 1, and 8 kHz, but not at 2 and 4 kHz. These results suggest that improvements in threshold for long-duration stimuli during infancy may not be accompanied by comparable changes in threshold at short durations. The delayed development of sensitivity to low- and high-frequency clicks appears consistent with maturational trends recently described for the auditory brainstem response.     

Underwater audiogram of the California sea lion by the conditioned vocalization technique

Conditioning techniques were developed demonstrating that pure tone frequencies under water can exert nearly perfect control over the underwater click vocalizations of the California sea lion (Zalophus californianus). Conditioned vocalizations proved to be a reliable way of obtaining underwater sound detection thresholds in Zalophus at 13 different frequencies, covering a frequency range of 250 to 64,000 Hz. The audiogram generated by these threshold measurements suggests that under water, the range of maximal sensitivity for Zalophus lies between one and 28 kHz with best sensitivity at 16 kHz. Between 28 and 36 kHz there is a loss in sensitivity of 60 dB/octave. However, with relatively intense acoustic signals (> 38 dB re 1 μb underwater), Zalophus will respond to frequencies at least as high as 192 kHz. These results are compared with the underwater hearing of other marine mammals.     

汉语听觉阈下启动效应：来自听觉掩蔽启动范式的证据

使用汉语双字词为实验材料,采用听觉掩蔽启动范式,通过3个实验考察汉语听觉阈下启动效应。结果发现,真词的听觉阈下重复启动效应显著,并且听觉阈下重复启动效应不受启动、目标发音者性别一致性的影响。但真词的阈下语音、语素和语义启动效应及假词的阈下重复和首字启动效应都不显著。这些结果说明,听觉通道阈下呈现的汉语双字词的词汇水平信息可以得到无意识加工。汉语双字词的听觉阈下启动效应可能是基于启动词整词表征的无意识激活。     

Some properties of the olfactory system of man

Preliminary investigations into the effects of a 12-h diurnal variation suggested there was a 10-fold decrease in odor sensitivity from morning to evening. For a selected group of odorants (methyl, t-butyl, and phenyl isonitrile), the difference between detection and recognition thresholds in general was found to be 10-fold; however, for some Ss the difference was less. When Ss were blindfolded, no changes in odor sensitivity were noted. Similarly, imposing an auditory stress on the test situation did not significantly alter odor sensitivity in either experienced or naive Ss,     

Duration discrimination by musicians and nonmusicians

This study investigated the effects of stimulus modality, standard duration, sex, and laterality in duration discrimination by musicians and nonmusicians. Seventeen musicians (M age = 24.1 yr.) and 22 nonmusicians (M age = 26.8 yr.) participated. Auditory (1,000 Hz) and tactile (250 Hz) sinusoidal suprathreshold stimuli with varying durations were used. The standard durations tested were 0.5 and 3.0 sec. Participants discriminated comparison stimuli which had durations slightly longer and shorter than the standard durations. Difference limens were found by the method of limits and converted to Weber fractions based on the standard durations. Musicians had lower, i.e., better, Weber fractions than nonmusicians in the auditory modality, but there was no significant difference between musicians and nonmusicians in the tactile modality. Auditory discrimination was better than tactile discrimination. Discrimination improved when the standard duration was increased both for musicians and nonmusicians. These results support previous findings of superior auditory processing by musicians. Significant differences between discrimination in the millisecond and second ranges may be due to a deviation from Weber's law and the discontinuity of timing in different duration ranges reported in the literature.     

Auditory frequency sensitivity in the neonate: a signal detection analysis.

Using signal detectability theory, an analysis was performed on some auditory frequency sensitivity data obtained in 1968 by Hutt et al. on human neonates. The d′-values over the frequencies from 70 Hz to 2kHz formed a significant cubic function. No state of arousal effects were found on sensitivity, as had been found in 1968. The β-values did not vary systematically with state, which suggests that levels of arousal should be studied separately. It is also suggested that the complex sensitivity found may provide a mechanism by which neonates may monitor their own vocalizations.     

The effect of vibrato on the recognition of masked vowels

Five experiments on the identifiability of synthetic vowels masked by wideband sounds are reported. In each experiment, identification thresholds (signal/masker ratios, in decibels) were measured for two versions of four vowels: a vibrated version, in which FO varied sinusoidally around 100 Hz; and a steady version, in which F0 was fixed at 100 Hz. The first three experiments were performed on naive subjects. Experiment 1 showed that for maskers consisting of bursts of pink noise, vibrato had no effect on thresholds. In Experiment 2, where the maskers were periodic pulse trains with an F0 randomly varied between 120 and 140 Hz from trial to trial, vibrato slightly improved thresholds when the sound pressure level of the maskers was 40 dB, but had no effect for 65-dB maskers. In Experiment 3, vibrated rather than steady pulse trains were used as maskers; when these maskers were at 40 dB, the vibrated versions of the vowels were slightly less identifiable than their steady versions; but, as in Experiment 2, vibrato had no effect when the maskers were at 65 dB. Experiment 4 showed that the unmasking effect of vibrato found in Experiment 2 disappeared in subjects trained in the identification task. Finally, Experiment 5 indicated that in trained listeners, vibrato had no influence on identification performance even when the maskers and the vowels had synchronous onsets and offsets. We conclude that vibrating a vowel masked by a wideband sound can affect its identification threshold, but only for tonal maskers and in untrained listeners. This effect of vibrato should probably be considered as a Gestalt phenomenon originating from central auditory mechanisms.     

Stroop effects for masked threat words: Pre‐attentive bias or selective awareness?

The single‐trial emotional Stroop effect for masked threat words, and its association with anxiety, anger, and depression was studied in a group of men (n = 24) and women (n = 24) while controlling for possible differential thresholds for threat words versus neutral words. Stroop interference for masked threat words was found to correlate with trait anxiety, and the effect could not be explained by any differences in thresholds due to valence, neither at a subjective (conscious identification task) nor at an objective (lexical decision task) level of awareness. Jacoby's exclusion task was explored as an alternative measure of conscious awareness, and the results corroborated the conclusion that the Stroop effect for masked threat words was the result of preattentive processes. Unexpectedly, however, the correlation between Stroop interference for masked threat words and trait anxiety was found only among the men.     

Avoidance learning facilitates temporal processing in the primary auditory cortex

The primary auditory cortex is now known to be involved in learning and memory, as well as auditory perception. For example, spectral tuning often shifts toward or to the frequency of the conditioned stimulus during associative learning. As previous research has focused on tonal frequency, less is known about how learning might alter temporal parameters of response in the auditory cortex. This study addressed the effects of learning on the fidelity of temporal processing. Adult male rats were trained to avoid shock that was signaled by an 8.0 kHz tone. A novel control group received non-contingent tone and shock with shock probability decreasing over days to match the reduced number of shocks received by the avoidance group as they mastered the task. An untrained (nai ve) group served as a baseline. Following training, neuronal responses to white noise and a broad spectrum of tones were determined across the primary auditory cortex in a terminal experiment with subjects under general anesthesia. Avoidance conditioning significantly improved the precision of spike-timing: the coefficient of variation of 1st spike latency was significantly reduced in avoidance animals compared to controls and nai ves, both for tones and for noise. Additionally, avoidance learning was accompanied by a reduction of the latency of peak response, by 2.0-2.5 ms relative to nai ves and approximately 1.0 ms relative to controls. The shock-matched controls also exhibited significantly shorter peak latency of response than nai ves, demonstrating the importance of this non-avoidance control. Plasticity of temporal processing showed no evidence of frequency specificity and developed independently of the non-temporal parameters magnitude of response, frequency tuning and neural threshold, none of which were facilitated. The facilitation of temporal processing suggests that avoidance learning may increase synaptic strength either within the auditory cortex, in the subcortical auditory system, or both.     

Behavioral limits of auditory temporal resolution in the rat: amplitude modulation and duration discrimination

Thresholds for detecting the presence of amplitude modulation in a noise carrier were determined for rats using conditioned avoidance procedures. There was a progressive increase in threshold with modulation rates between 5 Hz and 2 kHz. Further tests were conducted to determine difference thresholds for detecting an increase in modulation rate for standard rates of 10, 50, and 100 Hz. The size of the difference threshold increased progressively as the standard rate increased. In addition, thresholds for detecting an increase in the duration of a noise burst were determined for various standard durations. The difference thresholds were constant for values between 10 and 50 ms but increased progressively, with standard durations between 0.1 and 1.0 s.     

Impaired sensitivity to dynamic stimuli in poor readers of a regular orthography

The mappings from grapheme to phoneme are much less consistent in English than they are for most other languages. Therefore, the differences found between English-speaking dyslexics and controls on sensory measures of temporal processing might be related more to the irregularities of English orthography than to a general deficit affecting reading ability in all languages. However, here we show that poor readers of Norwegian, a language with a relatively regular orthography, are less sensitive than controls to dynamic visual and auditory stimuli. Consistent with results from previous studies of English-readers, detection thresholds for visual motion and auditory frequency modulation (FM) were significantly higher in 19 poor readers of Norwegian compared to 22 control readers of the same age. Over two-thirds (68.4%) of the children identified as poor readers were less sensitive than controls to either or both of the visual coherent motion or auditory 2Hz FM stimuli.     

Speech and non-speech processing in people with specific language impairment: a behavioural and electrophysiological study

McArthur and Bishop (2004) found that people with specific language impairment (SLI) up to 14 years of age have poor behavioural frequency discrimination (FD) thresholds for 25-ms pure tones, while people with SLI upto 20 years of age have abnormal auditory N1--P2--N2 event-related potential (ERP) responses to the same tones. In the present study, we extended these findings to more complex non-speech and speech sounds by comparing younger (around 13 years) and older (around 17 years) teenagers with SLI and controls for their behavioural FD thresholds and N1-P2 ERPs to 25 and 250-ms pure tones, vowels, and non-harmonic complex tones. We found that a subgroup of people with SLI had abnormal responses to tones and vowels at the level of behaviour and the brain, and that poor processing was associated with the spectral complexity of auditory stimuli rather than their phonetic significance. We suggest that both the age of listeners and the sensitivity of psychoacoustic tasks to age-related changes in auditory skills may be crucial factors in studies of sound processing in SLI.     

Auditory sensitivity in school-age children

Thresholds for octave-band noises with center frequencies of 0.4, 1, 2, 4, and 10 kHz and 1/3-octave-band noises centered at 10 and 20 kHz were obtained from children 6 to 16 years of age. Such thresholds, combined with those obtained previously for infants, preschool children, and adults, provide a detailed picture of developing auditory sensitivity between infancy and maturity. Continuing improvements in sensitivity are evident from infancy through the preschool period, well into the school years. For stimuli with center frequencies of 0.4 and 1 kHz, maximal sensitivity is achieved at about 10 years of age, compared to 8 years for stimuli of 2 and 4 kHz. For 10-kHz stimuli, there is little change beyond 4 or 5 years of age. Finally, 20-kHz stimuli yield maximal sensitivity at about 6 or 8 years of age, followed by a progressive decline to adult levels. These findings are considered in relation to auditory sensitivity in nonhuman species, to structural and functional development of the ear, and to possible changes in the efficiency of neural processing.     

Cross-modal facilitation in speech prosody

Speech prosody has traditionally been considered solely in terms of its auditory features, yet correlated visual features exist, such as head and eyebrow movements. This study investigated the extent to which visual prosodic features are able to affect the perception of the auditory features. Participants were presented with videos of a speaker pronouncing two words, with visual features of emphasis on one of these words. For each trial, participants saw one video where the two words were identical in both pitch and amplitude, and another video where there was a difference in either pitch or amplitude that was congruent or incongruent with the visual changes. Participants were asked to decide which video contained the sound difference. Thresholds were obtained for the congruent and incongruent videos, and for an auditory-alone condition. It was found that the congruent thresholds were better than the incongruent thresholds for both pitch and amplitude changes. Interestingly, the congruent thresholds for amplitude were better than for the auditory-alone condition, which implies that the visual features improve sensitivity to loudness changes. These results demonstrate that visual stimuli can affect auditory thresholds for changes in pitch and amplitude, and furthermore support the view that visual prosodic features enhance speech processing.     

A detector of sonic and ultrasonic vocalizations with frequency readout

An electronic apparatus to detect vocalizations between 4 and 50 kHz and to provide frequency readout is described. A frequency-to-voltage converter changes vocalizations to their analog. A peak-and-hold circuit retains and gates the maximal value of this analog voltage while it is accessed by a chart recorder or computer. Provision is made to lock out noise by inhibiting the device’s response to all signals lower than those associated with a selectable cutoff frequency. In preliminary tests of the apparatus, vocal signals of two rats in a common cage were recorded while the animals were subjected to a brief, intermittent bout of faradic shock to the feet. All recorded vocalizations occurred at frequencies below 26 kHz.     

Sex differences in fetal habituation

There is some evidence for sex differences in habituation in the human fetus, but it is unknown whether this is due to differences in central processing (habituation) or in more peripheral processes, sensory or motor, involved in the response. This study examined whether the sex of the fetus influenced auditory habituation at 33 weeks of gestation, and whether this was due to differences in habituation or in the sensory or motor components using a set of four experiments. The first experiment found that female fetuses required significantly fewer stimulus presentations to habituate than males. The second experiment revealed no difference in the spontaneous motor behaviour of male and female fetuses. The third experiment examined auditory intensity thresholds for the stimuli used to habituate the fetus. No differences in thresholds were found between males and females, although there was inter-individual variability in thresholds. A final experiment, using stimuli individualized for that particular fetus' auditory intensity threshold, found that female fetuses habituated faster than males. In combination, the studies reveal that habituation in the human fetus is affected by sex and this is due to a difference in central 'information processing' of the stimuli rather than peripheral aspects of the response. It is argued that male and female fetuses present different neurobehavioural developmental trajectories, with females more advanced at 33 weeks than males. This study suggests that research examining prenatal behaviour should consider the factor of fetal sex. This may be particularly pertinent where there is an intention to use the results diagnostically.