Reflex modification in the rat: the inhibitory effects of intensity and frequency changes in steady tones

In laboratory rats (as in humans) a low-intensity tone that precedes a high-intensity burst of noise by approximately 100 ms can reduce the amplitude of the startle reaction elicited by the burst of noise. A series of four experiments with rats investigated the relation between the inhibitory effects of tonal frequency change and the length of the silent period (gap) preceding it. The major findings were the following: (a) A gap in an otherwise continuous pure tone inhibited startle when the gap occurred approximately 100 ms prior to the noise burst. (b) Although an increase in gap duration increased the inhibition afforded by the gap, the maximum inhibition was yielded by gaps of 100 ms and greater; this maximum was equivalent to the inhibition yielded by the presentation of a postgap tone alone. (c) A shift in tonal frequency across a 10-ms gap yielded more inhibition than did the same gap with no frequency shift; again the shift yielded equivalent inhibition to the presentation of the postgap tone alone. (d) An increase in the frequency shift increased inhibition when the shift occurred across a 10-ms gap, but not when the shift occurred across a 100-ms gap.     

Modification of the human glabella reflex by antecedent acoustic stimulation

The eyeblink elicited by a mechanically produced tap to the glabella was inhibited by a 50-msec, 80-dB SPL tone presented in the interval 50 to 800 msec prior to the tap, but maximal inhibition occurred when the lead interval was 100 msec. At this lead interval, the amount of inhibition was an increasing function of prestimulus intensity, but reliable inhibition was detected when prestimulus intensity was only 30 dB SPL. With a given inhibitory prestimulus, the amount of inhibition was independent of the intensity of the blink-eliciting tap. Monaural presentation of a prestimulus was found to produce more inhibition than the binaural presentation of that same prestimulus. The offset of an otherwise continuous binaural acoustic signal 100 msec prior to a tap inhibited the eyeblink, but more inhibition was found when offset occurred in only one ear.     

Inhibition of the glabella reflex by monaural and binaural stimulation

The human eyeblink, elicited by a tap to the glabella, can be inhibited if a relatively weak acoustic signal precedes the tap by approximately 100 msec. The work reported here was designed to explore the surprising fact that more inhibition occurs when the acoustic prestimulation is presented monaurally than when it is presented binaurally. The present studies revealed that (a) given equally loud binaural inputs, a reduction of about 40 dB(A) in one of them is sufficient to produce inhibition comparable to that produced by a monaural signal, (b) the difference between nonaural and binaural inhibition remains constant as the intensity of prestimulation is varied, and (c) the simultaneous offset of a tone in one ear and onset of a tone in the other ear produces more inhibition than either monaural offest or onset alone. These findings suggest that the specific attributes of a given acoustic signal make independent contributions to the inhibition produced by that signal.     

Acoustic augmentation and inhibition of the human eyeblink

The human eyeblink elicited by a mechanically produced tap to the glabella was inhibited by a mild acoustic stimulus presented 200 msec prior to the tap and was augmented when the same acoustic stimulus was presented simultaneously with the tap. Monaural presentation of the acoustic stimulus prior to the tap yielded more reflex inhibition than when that same stimulus was presented binaurally. Binaural presentation of the acoustic stimulus simultaneously with the tap yielded more reflex augmentation than when that same stimulus was presented monaurally. These findings lend credence to the proposition that reflex inhibition and reflex augmentation are mediated by separate neural pathways.     

Reflex augmentation of a tap-elicited eyeblink: the effects of tone frequency and tap intensity

The amplitude of the human eyeblink elicited by a mild tap between the eyebrows can be increased if a brief tone is presented simultaneously with the tap. In two experiments we examined how this reflex augmentation effect varies with changes in the frequency characteristics of the tone and with changes in the intensity of the tap. We also examined how these effects change in the course of development. For newborn infants and for adults, fixed intensity tones with frequencies of either 1, 2, or 4 kHz produced equivalent amounts of reflex augmentation. Furthermore, while blink amplitude was an increasing function of tap intensity in both populations, the amount of reflex augmentation engendered by a simultaneously presented tone was independent of the intensity of the tap.     

Auditory-visual conflicts in the perceived duration of lights, tones and gaps

The perceived duration of a short tone (1,000 or 1,500 msec) was longer than that of a separately presented light of equal length. Thus, when light and tone were presented simultaneously, there was a conflict in perceived duration. In that case, the perceived duration of an interval filled with both light and tone was close to that of an interval filled with tone alone. A silent gap in otherwise continuous tone was perceived as longer than a gap in otherwise continuous light, and the perceived duration of a gap occurring simultaneously in both light and tone was close to that of a gap in tone alone. Thus, auditory dominance occurred under the preceding conditions-that is, auditory-visual conflicts in perceived duration, whether occurring between filled intervals or gaps, were resolved in favor of the auditory modality. Visual dominance occurred only under one condition, in which the intensity of tone was reduced, and in which the perceived duration of a 500-msec light was longer than that of a 500-msec tone. The finding of auditory dominance in the perception of time runs counter to the results of studies of sensory conflicts in spatial perception, where vision typically dominates audition and touch.     

PHONOLOGY IN THE LEXICAL PROCESSING OF CHINESE: PRIMING TONE NEIGHBOURS

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Phonology in the Lexical Processing of Chinese: Priming Tone Neighbors

Using both visual-visual and auditory-visual priming lexical decision tasks, this study investigated phonological processing in reading logographic Chinese. Compound words sharing segmental templates but differing in lexical tones were used as primes and targets while their relative frequency was manipulated. It was found that tone neighbours did not prime each other significantly and the SOA of 100 msec in visual-visual priming. When the SOA was increased to 357 msec, or when primes were presented auditorily, the processing of target words was significantly delayed by their tone neighbours. Larger inhibitory effects were observed for low frequency targets with high frequency primes. It was argued that although phonological information is automatically activated and this activation affects access to semantics in reading Chinese,phonological mediation is not the only or the main ~urce of constraints on semantic activation.     

Pitch memory for short tones

Ten listeners judged a 300-msec tone as higher or lower in pitch than another 300-msec tone that occurred 8 sec earlier. The intervening time either was unfilled or contained a 400-msec interpolated tone. This interpolated tone occurred either just after the first tone or just before the final one, and was of a frequency either inside or outside the critical band of the target frequency. Performance for the silent-interval condition was about as good as has been reported for pitch discrimination with no delay when the target was 250 Hz but was slightly poorer for the target at 1,550 Hz. Presence of the interpolated tone decreased the slope of the psychometric [unction and produced constant error for nine Ss. These effects were more pronounced when the interpolated tone occurred 50 msec after the target than when it preceded the comparison tone by 50 msec. Both brevity of the target tone and occurrence soon thereafter of an interpolated tone are required to produce constant errors of pitch memory.     

Fixation point offsets facilitate endogenous saccades

Subjects produced saccades to continuously visible targets that were signaled by the pitch, not the location, of an auditory signal. Such endogenous saccades were initiated more quickly when the visual fixation point disappeared 200 msec before the signal (thus producing a “gap”), even though the alerting benefits of such a warning were eliminated by an earlier warning tone. The presence of the gap effect under these circumstances shows that the effect is more general than was previously believed: Visual fixation point offsets facilitate saccades by affecting oculomotor processes related to both visually elicited (exogenous) and centrally produced (endogenous) saccades. In addition, the magnitude of the gap effect for endogenous saccades was significantly smaller than that for exogenous saccades, suggesting that at least some of the effect arises in relatively early processes, such as those involved in the processing of sensory signals, and not exclusively in later processes, such as those involved in the preparation and production of saccades.     

Modulation of the acoustic startle reflex in humans in the absence of anticipatory changes in the middle ear reflex

If a weak tone precedes an intense tone, then the acoustic startle eyeblink reflex elicited by the stronger stimulus is inhibited. It has been suggested that the leading stimulus gives rise to a protective middle ear reflex that attenuates the effective intensity of the second. This hypothesis was tested and disproved. In seven subjects intense tone bursts sufficient to elicit both intratympanic and eyeblink responses were presented sometimes alone and sometimes preceded at various lead times (25 to 400 msec) by a weak tone. The weak tone inhibited the amplitude of the eye blink to the strong tone, maximally at intervals of 100 to 200 msec, but was never seen to produce any of the anticipatory impedance changes that would be characteristic of middle ear reflex activity during the interval between the two stimuli.     

Temporal discrimination as a function of marker duration

In a series of three experiments, the effect of marker duration on temporal discrimination was evaluated with empty auditory intervals bounded by markers ranging from 3 to 300 msec or presented as a gap within a continuous tone. As a measure of performance, difference thresholds in relation to a base duration of 50 msec were computed. Performance on temporal discrimination was significantly better with markers ranging from 3 to 150 msec than with markers ranging from 225 to 300 msec or under the gap condition. However, within each range of marker duration (3–150 msec; 225–300 msec or gap) performance did not differ significantly. A fourth experiment provided evidence that the effect of marker duration cannot be explained in terms of marker-induced masking. A good approximation of the relationship between marker duration and temporal discrimination performance in the present experiments is a smooth step function, which can account for 99.3% of the variance of mean discrimination performance. Thus, the findings of the present study point to the conclusion that two different mechanisms are used in the processing of temporal information, depending on the duration of the auditory markers. The tradeoff point for the hypothetical shift from one timing mechanism to the other may be found at a marker duration of approximately 200 msec.     

Illusory recouplings of onsets and terminations of glide tone components

We present a new auditory illusion, the gap transfer illusion, supported by phenomenological and psychophysical data. In a typical situation, an ascending frequency glide of 2,500 msec with a temporal gap of 100 msec in the middle and a continuously descending frequency glide of 500 msec cross each other at their central positions. These glides move at the same constant speed in logarithmic frequency in opposite directions. The temporal gap in the long glide is perceived as if it were in the short glide. The same kind of subjective transfer of a temporal gap can take place also when the stimulus pattern is reversed in time. This phenomenon suggests that onsets and terminations of glide components behave as if they were independent perceptual elements. We also find that when two long frequency glides are presented successively with a short temporal overlap, a long glide tone covering the whole duration of the pattern and a short tone around the temporal middle can be perceived. To account for these results, we propose an event construction model, in which perceptual onsets and terminations are coupled to construct auditory events and the proximity principle connects these elements.     

Pitch perception and retention: two cumulative benefits of selective attention

By presenting, before a "chord" of three pure tones with remote frequencies, a tone relatively close in frequency to one component (T1) of the chord, one can direct the listener's attention onto T1 within the chord. In the first part of the present study, it was found that this increases the accuracy with which the pitch of T1 is perceived. The attentional cue improved the discrimination between the frequency of T1 and that of another tone (T2) presented immediately after the chord or very shortly (300 msec) after it. No improvement was found when T1 was presented alone instead of within a chord. A subsequent experiment, in which the chord and T2 were separated by either 300 msec or 4 sec, indicated that the attentional cue improved not only the perception, but also the memorization of the pitch of T1 (especially when T1 was the intermediate component of the chord). It is argued that the positive effect of attention on memory took place when the pitch percept was encoded into memory, rather than after the formation of the pitch memory trace.     

Differences in American English, Spanish, and monkey perception of the say-stay trading relation

An interesting phenomenon in human speech perception is the trading relation, in which two different acoustic cues both signal the same phonetic percept. The present study compared American English, Spanish, and monkey listeners in their perception of the trading relation between gap duration and F1 transition onset frequency in a synthetic say-stay continuum. For all the subjects, increased gap duration caused perception to change from say to stay; however, subjects differed in the extent to which the F1 cue traded with gap duration. For American English listeners, a change from a low to a high F1 onset caused a phoneme boundary shift of 26 msec toward shorter gap durations, indicating a strong trading relation. For Spanish listeners, the shift was significantly smaller at 13.7 msec, indicating a weaker trading relation. For monkeys, there was no shift at all, indicating no trading relation. These results provide evidence that the say-stay trading relation is dependent on perceptual learning from linguistic exposure.     

A comparison of classical eyelid conditioning in adults and infants

In a classical conditioning procedure an eyeblink-eliciting tap to the glabella (the flat region of skin between the eyebrows) was presented 500 ms after the onset of a mild l-kHz tone. As tone-tap presentations proceeded, the probability of an eyeblink during the latter part of the tone increased in both infants (median age 8 months) and adults, but the infants were slower to condition than the adults and were more variable. Overall, the latency of the conditioned response to tone was significantly longer for infants than for adults, but the latency of the unconditioned response to tap was significantly shorter for infants than for adults.     

Frequency recognition in temporal interference tasks: A comparison among four psychophysical procedures

The frequency discrimination of a 20-msec test tone was measured for the same subjects in four psychophysical paradigms: a single-interval procedure, a two-alternative forced-choice procedure, a same-different procedure, and a method-of-adjustment procedure. In each paradigm, the 20-msec test tone was preceded or followed by a 500-msec, 800-Hz interfering tone. The interfering tone occurred 50 or 5 msec before the onset of the test tone (forward interference) or 100 or 5 msec after the offset of the test tone (backward interference). In each of the four paradigms and for each of the interference conditions the value of Δf for the test tone was varied symetrically around 800 Hz to obtain an estimate of the frequency discrimination thresholds. In all psychophysical paradigms except for the single-interval procedure, there were small or no significant differences in observers’ frequency discrimination behavior among the interference conditions. The thresholds for Δf from these conditions were approximately the same as those obtained without an interfering tone. In the single-interval task, when the test tone preceded the interfering tone (backward interference) by 5 msec, an increase in the value of Δf required for discrimination over that required in the other conditions was measured. These results suggest that the effect of backward interference on a target tone does depend on psychophysical procedure.     

Differences in American English, Spanish, and monkey perception of thesay-stay trading relation

An interesting phenomenon in human speech perception is the trading relation, in which two different acoustic cues both signal the same phonetic percept. The present study compared American English, Spanish, and monkey listeners in their perception of the trading relation between gap duration andFl transition onset frequency in a syntheticsay-stay continuum. For all the subjects, increased gap duration caused perception to change fromsay tostay; however, subjects differed in the extent to which theFl cue traded with gap duration. For American English listeners, a change from a low to a highF1 onset caused a phoneme boundary shift of 26 msec toward shorter gap durations, indicating a strong trading relation. For Spanish listeners, the shift was significantly smaller at 13.7 msec, indicating a weaker trading relation. For monkeys, there was no shift at all, indicating no trading relation. These results provide evidence that thesay-stay trading relation is dependent on perceptual learning from linguistic exposure.     

Feature processing during high-rate auditory selective attention

Auditory event-related brain potentials (ERPs) and reaction times were, analyzed in a selective attention task in which subjects attended to tone pips presented at high rates-Xinterstimulua intervals [ISIs] of 40-200 msec). Subjects responded to infrequent target tones of a specified frequency (250 or 4000 Hz) and location (left or right ear) that were louder than otherwise identical tones presented randomly to the left and right ears. Negative difference (Nd) waves were isolated by subtracting ERPs to tones with no target features from ERPs to the same tones when they shared target location, frequency, or both frequency and location cues. Nd waves began 60-70 msec after tone onset and lasted until 252–350 msec after tone onset, even for tones with single attended cues. The duration of Nd waves exceeded the ISIs between successive tones, implying that several stimuli underwent concurrent analysis. Nd waves associated with frequency processing had scalp distributions different from those associated with location processing, implying that the features were analyzed in distinct cortical areas. Nd waves specific to auditory feature conjunction were isolated. These began at latencies of 110–120 msec, some 30-40 msec after the Nds to single features. The relative timing of the different Nd waves suggests that auditory feaure conjunction begins after a brief parallel analysis of individual features but before feature analysis is complete.     

Studies in auditory timing: 1. Simple patterns

Listeners' accuracy in discriminating one temporal pattern from another was measured in three psychophysical experiments. When the standard pattern consisted of equally timed (isochronic) brief tones, whose interonset intervals (IOIs) were 50, 100, or 200 msec, the accuracy in detecting an asynchrony or deviation of one tone in the sequence was about as would be predicted from older research on the discrimination of single time intervals (6%-8% at an IOI of 200 msec, 11%-12% at an IOI of 100 msec, and almost 20% at an IOI of 50 msec). In a series of 6 or 10 tones, this accuracy was independent of position of delay for IOIs of 100 and 200 msec. At 50 msec, however, accuracy depended on position, being worst in initial positions and best in final positions. When one tone in a series of six has a frequency different from the others, there is some evidence (at IOI = 200 msec) that interval discrimination is relatively poorer for the tone with the different frequency. Similarly, even if all tones have the same frequency but one interval in the series is made twice as long as the others, temporal discrimination is poorer for the tones bordering the longer interval, although this result is dependent on tempo or IOI. Results with these temporally more complex patterns may be interpreted in part by applying the relative Weber ratio to the intervals before and after the delayed tone. Alternatively, these experiments may show the influence of accent on the temporal discrimination of individual tones.