Second-order schedules with paired auditory brief stimuli

Pigeons were exposed to multiple second-order schedules of paired and unpaired brief stimuli in which responding on the main key was reinforced according to a fixed-interval thirty-second schedule by a brief stimulus (a tone in the paired schedule) and advancement to the next segment of the second-order schedule. In Experiment 1, a response on the second key was required during the tone in its fourth and final presentation to produce food. Responses during earlier brief stimuli indicated the extent to which the final brief stimulus was discriminated from preceding ones. Responding was comparable during all tones, extending prior findings with visual paired brief stimuli and weakening explanations of subjects' failure to discriminate between brief-stimulus presentations in terms of elicited responding. In Experiment 2 the number of fixed-interval segments comprising the second-order schedules varied from one through eight. Although main-key response rates increased across segments in both experiments, they increased much less sharply with a variable number of segments. These results suggest that the increase in main-key response rates across segments is due primarily to a degree of temporal discrimination not reflected on the second key. Main-key response rates were higher on paired auditory brief-stimulus schedules than on unpaired visual brief-stimulus schedules, especially in Experiment 2, thus further extending findings with visual brief stimuli to second-order schedules with auditory brief stimuli.     

Visual dominance in the pigeon

In Experiment 1, three pigeons were trained to obtain grain by depressing one foot treadle in the presence of a 746-Hertz tone stimulus and by depressing a second foot treadle in the presence of a red light stimulus. Intertrial stimuli included white light and the absence of tone. The latencies to respond on auditory element trials were as fast, or faster, than on visual element trials, but pigeons always responded on the visual treadle when presented with a compound stimulus composed of the auditory and visual elements. In Experiment 2, pigeons were trained on the auditory-visual discrimination task using as trial stimuli increases in the intensity of auditory or visual intertrial stimuli. Again, pigeons showed visual dominance on subsequent compound stimulus test trials. In Experiment 3, on compound test trials, the onset of the visual stimulus was delayed relative to the onset of the auditory stimulus. Visual treadle responses generally occurred with delay intervals of less than 500 milliseconds, and auditory treadle responses generally occurred with delay intervals of greater than 500 milliseconds. The results are discussed in terms of Posner, Nissen, and Klein's (1976) theory of visual dominance in humans.     

Separate "what" and "where" decision mechanisms in processing a dichotic tonal sequence.

Right-handed subjects were presented with a dichotic tonal sequence, whose basic pattern consisted of three 800-Hz tones followed by two 400-Hz tones on the channel and simultaneously three 400-Hz tones followed by two 800-Hz tones on the other. All tones were 250 msec in duration and separated by 250-msec pauses. On any given stimulus presentation, most subjects reported the sequence of pitches delivered to one ear and ignored the other. They further tended significantly to report the sequence delivered to the right ear rather than to the left. However, each tone appeared to be localized in the ear receiving the higher frequency, regardless of which ear was followed for pitch and regardless of whether the higher or lower frequency was in fact perceived.     

The effect of exogenous spatial attention on auditory information processing

This study investigated the effect of exogenous spatial attention on auditory information processing. In Experiments 1, 2 and 3, temporal order judgment tasks were performed to examine the effect. In Experiment 1 and 2, a cue tone was presented to either the left or right ear, followed by sequential presentation of two target tones. The subjects judged the order of presentation of the target tones. The results showed that subjects heard both tones simultaneously when the target tone, which was presented on the same side as the cue tone, was presented after the target tone on the opposite side. This indicates that spatial exogenous attention was aroused by the cue tone, and facilitated subsequent auditory information processing. Experiment 3 examined whether both cue position and frequency influence the resulting information processing. The same effect of spatial attention was observed, but the effect of attention to a certain frequency was only partially observed. In Experiment 4, a tone fusion judgment task was performed to examine whether the effect of spatial attention occurred in the initial stages of hearing. The result suggests that the effect occurred in the later stages of hearing.     

Effects of redundant auditory stimuli on reaction time

Auditory redundancy gains were assessed in two experiments in which a simple reaction time task was used. In each trial, an auditory stimulus was presented to the left ear, to the right ear, or simultaneously to both ears. The physical difference between auditory stimuli presented to the two ears was systematically increased across experiments. No redundancy gains were observed when the stimuli were identical pure tones or pure tones of different frequencies (Experiment 1). A clear redundancy gain and evidence of coactivation were obtained, however, when one stimulus was a pure tone and the other was white noise (Experiment 2). Experiment 3 employed a two-alternative forced choice localization task and provided evidence that dichotically presented pure tones of different frequencies are apparently integrated into a single percept, whereas a pure tone and white noise are not fused. The results extend previous findings of redundancy gains and coactivation with visual and bimodal stimuli to the auditory modality. Furthermore, at least within this modality, the results indicate that redundancy gains do not emerge when redundant stimuli are integrated into a single percept.     

Long latency auditory evoked potentials

Experiment 1 elicited the P1, N1, P2, and N2 components of the long latency auditory evoked potential (AEP) using a 1000 Hz tone presented at 30, 50, or 70 dB SPL and 1-, 3-, or 5- second inter-stimulus intervals to assess the relative effects of the combination of these variables on component amplitude and latency. Four blocks of 16 tone presentations each were recorded from each subject to determine if changes in the AEP would occur because of short-term habituation. Both stimulus factors interacted significantly in a systematic fashion for the amplitude measures, with increases in latency also associated with increases in intensity and inter-stimulus interval. Only minor changes across the four trial blocks for either the amplitude or latency measures were observed over the various stimulus presentation conditions. Experiment 2 employed the same tone stimulus presented at 50 dB SPL and a 3-second inter-stimulus interval. Eight blocks of 64 trials were recorded from each subject on each day for four days to investigate long-term habituation effects. No substantial changes in any of the component amplitudes or latencies were obtained across the 32 trial blocks. It was concluded that intensity and inter-stimulus interval interact to determine AEP amplitude as well as latency values and that the constituent components do not change appreciably with repeated stimulus presentations, even after several days.     

时距的短时保持: 缩短还是变长

采用Wearden和Ferrara(1993)的经典方法, 分别考察了1s以下(350 ms~650 ms)和1s以上(1000 ms ~ 2000 ms)不同类型(空、实时距)和通道(视、听)时距的短时保持效应。实验1发现, 不同刺激通道条件下, 1s以下时距的短时保持都呈现出主观缩短, 其中视觉条件比听觉条件明显; 实验2表明, 1s以上时距在不同刺激通道条件下都呈现出主观变长, 其中听觉条件比视觉条件明显。分析表明, 主观缩短趋势可能是由主观缩短效应和正的顺序误差效应共同作用所致, 而主观变长趋势是由主观变长效应和负的顺序误差效应造成的。     

Second-order autoshaped key pecking based on an auditory stimulus.

In Experiment 1, pigeons were exposed either to paired or to unpaired presentations of a tone and grain, and then to paired presentations of a keylight with the tone. Substantial second-order conditioned pecking to the keylight was produced in the birds that had received paired presentations of tone and grain. In Experiment 2, second-order pecking to the keylight increased in probability across four groups that had received, respectively, 20, 80, 140, or 200 paired presentations of tone and grain. In Experiment 3, the amount of pecking directed towards a keylight which predicted the first-order, tone CS was as substantial in birds without a prior history of key pecking as in birds with such a history. A further experiment failed to discover any significant differences in the levels of second-order pecking to a keylight paired with a first-order tone CS or with a first-order keylight CS. Thus, an auditory signal that does not itself support pecking may enable a localized visual stimulus to evoke key pecking.     

Subjective shortening in humans' memory for stimulus duration

Three experiments investigated memory for stimulus duration in humans using a modification of a delayed-matching technique previously used to study event memory in pigeons. In a session of 48 discrete trials subjects were presented with a sample stimulus (a 500-Hz tone with mean duration of 400 msec) then a comparison stimulus (the same duration as the sample, or longer or shorter), after a delay that was 1 to 10 sec in Experiments 1 and 2, and 2 to 16 sec in Experiment 3. After the comparison had been presented, subjects judged whether the sample and comparison had the same duration (a YES/NO decision, Experiment 1), or whether the comparison was longer, shorter, or of the same duration as the sample (Experiments 2 and 3). Overall, mean number of correct responses changed little with increases in the delay, but the change of number of correct responses with delay was markedly different on trials in which the sample and comparison were the same, the comparison was shorter, or the comparison was longer. In general, accuracy declined with increasing delay in the first case, remained constant in the second case, and increased when the comparison was longer than the sample. Examination of the types of errors made on the different sorts of trials (Experiment 3) suggested that the data were produced by two mechanisms: (1) subjective shortening of the sample as the delay between sample and comparison increased, and (2) a time-order error to respond that the sample was longer than the comparison. Overall, it appears that humans' working memory for duration exhibits a subjective shortening effect similar to that previously found in pigeons.     

The representation of pitch in auditory imagery: Evidence from S-R compatibility and distance effects

In three experiments we explored the nature of representations constructed during the perception and imagination of pitch. We employed a same–different task to eliminate the influence of nonauditory information and to minimise use of cognitive strategies on auditory imagery. A reference tone of frequency 1000, 1500, or 2000 Hz, or an imagined tone of a pitch indicated by a visual cue, was followed by a comparison tone (1000, 1500, or 2000 Hz) to which either a speeded same or different response was required. In separate experiments, same–different judgements were mapped to vertically (Experiments 1 and 2) and horizontally arranged responses (Experiment 3). Judgements of tones closer in pitch yielded longer reaction times and higher error rates than more distant tones, indicating a pitch distance effect for perceptual and imagery tasks alike. In addition, in the imagery task, same–different responses were faster when low-pitched tones demanded a bottom or left key response and high-pitched tones a top or right response than vice versa, suggesting that pitch is coded spatially. Together, these behavioural effects support the assumption that both perceived and imagined pitch are translated into an analogical representation in the spatial domain.     

Stimulus spacing effects in duration perception are larger for auditory stimuli: Data and a model

Models of duration bisection have focused on the effects of stimulus spacing and stimulus modality. However, interactions between stimulus spacing and stimulus modality have not been examined systematically. Two duration bisection experiments that address this issue are reported. Experiment 1 showed that stimulus spacing influenced the classification of auditory, but not visual, stimuli. Experiment 2 used a wider stimulus range, and showed stimulus spacing effects for both visual and auditory stimuli, although the effects were larger for auditory stimuli. A version of Temporal Range Frequency Theory was applied to the data, and was used to demonstrate that the qualitative pattern of results can be captured with the single assumption that the durations of visual stimuli are less discriminable from one another than are the durations of auditory stimuli.     

Effects of multimodal presentation and stimulus familiarity on auditory and visual processing

Two experiments examined the effects of multimodal presentation and stimulus familiarity on auditory and visual processing. In Experiment 1, 10-month-olds were habituated to either an auditory stimulus, a visual stimulus, or an auditory-visual multimodal stimulus. Processing time was assessed during the habituation phase, and discrimination of auditory and visual stimuli was assessed during a subsequent testing phase. In Experiment 2, the familiarity of the auditory or visual stimulus was systematically manipulated by prefamiliarizing infants to either the auditory or visual stimulus prior to the experiment proper. With the exception of the prefamiliarized auditory condition in Experiment 2, infants in the multimodal conditions failed to increase looking when the visual component changed at test. This finding is noteworthy given that infants discriminated the same visual stimuli when presented unimodally, and there was no evidence that multimodal presentation attenuated auditory processing. Possible factors underlying these effects are discussed.     

Spatial stimulus cue information supplying auditory saltation

Auditory saltation is a misperception of the spatial location of repetitive, transient stimuli. It arises when clicks at one location are followed in perfect temporal cadence by identical clicks at a second location. This report describes two psychophysical experiments designed to examine the sensitivity of auditory saltation to different stimulus cues for auditory spatial perception. Experiment 1 was a dichotic study in which six different six-click train stimuli were used to generate the saltation effect. Clicks lateralised by using interaural time differences and clicks lateralised by using interaural level differences produced equivalent saltation effects, confirming an earlier finding. Switching the stimulus cue from an interaural time difference to an interaural level difference (or the reverse) in mid train was inconsequential to the saltation illusion. Experiment 2 was a free-field study in which subjects rated the illusory motion generated by clicks emitted from two sound sources symmetrically disposed around the interaural axis, ie on the same cone of confusion in the auditory hemifield opposite one ear. Stimuli in such positions produce spatial location judgments that are based more heavily on monaural spectral information than on binaural computations. The free-field stimuli produced robust saltation. The data from both experiments are consistent with the view that auditory saltation can emerge from spatial processing, irrespective of the stimulus cue information used to determine click laterality or location.     

The ontogeny of auditory frequency generalization in the chicken.

To determine if there is an ontogenetic change in stimulus coding, chickens between the day of hatching and 9-10 days old were tested using a habituation-generalization paradigm. Experiment 1 indicated that 1 day-old and 3--4-day-old chicks show similar habituation of an eye-opening response to auditory stimuli in the 800--1,200-Hz range. In Experiment 2 the eye-opening response to a 1,000-Hz stimulus was habituated and then immediately tested using stimuli which varied between 800 and 1,200 Hz. Each age-group (1 day, 3--4 days, and 9--10 days) showed a symmetrical stimulus generalization gradient around the 1,000-Hz stimulus and the 1-day-old chicks displayed a reliably flatter gradient than either of the older groups, which did not differ. In a third experiment, the position of the gradients relative to the baseline was shifted without altering the relative shapes. These results allow general arousal, general auditory responsiveness, overall error rate, and metric characteristics of the independent and dependent variables to be eliminated as possible sources of the age differences in gradient shape. The changes in stimulus generalization, therefore, support the view that during normal development there is a sharpening of perceptual coding processes.     

Medial auditory thalamic input to the lateral pontine nuclei is necessary for auditory eyeblink conditioning

Auditory and visual conditioned stimulus (CS) pathways for eyeblink conditioning were investigated with reversible inactivation of the medial (MPN) or lateral (LPN) pontine nuclei. In Experiment 1, Long-Evans rats were given three phases of eyeblink conditioning. Phase 1 consisted of three training sessions with electrical stimulation of the medial auditory thalamic nuclei (MATN) paired with a periorbital shock unconditioned stimulus (US). An additional session was given with a muscimol (0.5 μL, 10 mM) or saline infusion targeting the LPN followed by a recovery session with no infusions. The same training and testing sequence was then repeated with either a tone or light CS in phases 2 and 3 (counterbalanced). Experiment 2 consisted of the same training as Experiment 1 except that muscimol or saline was infused in the MPN during the retention tests. Muscimol infusions targeting the LPN severely impaired retention of eyeblink conditioned responses (CRs) to the MATN stimulation and tone CSs but only partially reduced CR percentage to the light CS. Muscimol infusions that targeted the MPN had a larger effect on CR retention to the light CS relative to MATN stimulation or tone CSs. The results provide evidence that the auditory CS pathway necessary for delay eyeblink conditioning includes the MATN-LPN projection and the visual CS pathway includes the MPN.     

The relationship between reaction time and intensity in discrete auditory tasks

The effect of signal intensity upon reaction time (RT) was studied in three auditory RT tasks in which the signal was a tone of high or low frequency. Experiment I showed the well-known negative gradient with intensity of simple RT when the subject was instructed to ignore the frequency and give the same response to both tones. But when the subject had to discriminate the frequency in a choice RT task, the RT/intensity relationship appeared to be U-shaped. Experiment II showed that when the subject was required to make a response to one signal but withhold it for the other, a task which requires discrimination of the frequency of the tone but removes the necessity to choose between overt responses, no increase in RT at high intensities was obtained. The results indicate that it is the response choice stage rather than the stimulus encoding stage which is retarded at higher energy levels. Experiment I also demonstrated that visual and auditory leading signals have similar facilitating effects without affecting the RT/intensity relationships.     

Effects of pitch distance and likelihood on the perceived duration of deviant auditory events

When a deviant (oddball) stimulus is presented within a series of otherwise identical (standard) stimuli, the duration of the oddball tends to be overestimated. Two experiments investigated factors affecting systematic distortions in the perceived duration of oddball stimuli. Both experiments used an auditory oddball paradigm where oddball tones varied in both their pitch distance from the pitch of a standard tone and their likelihood of occurrence. Experiment 1 revealed that (1) far-pitch oddballs were perceived to be longer than near-pitch oddballs, (2) effects of pitch distance were greater in low-likelihood conditions, and (3) oddballs in later serial positions were perceived to be longer than oddballs in earlier serial positions. The above effects held regardless of whether oddballs were higher or lower in pitch than the standard. Experiment 2 revealed a pattern of response times in an oddball detection task that generally paralleled the pattern of data observed in Experiment 1; across conditions, there was a negative correlation between detection times and perceived duration. Taken together, the results suggest that the observed effects of oddball pitch, likelihood, and position on perceived duration are at least partly driven by how quickly individuals are able to initiate timing the oddball following its onset. Implications for different theoretical accounts of the oddball effect are discussed.     

Effect of stimulus pulse duration and interstimulus interval on cross-modal matching of auditory and lingual vibrotactile stimuli

Cross-modal matching functions for eight intensity levels of a 1000-Hz auditory stimulus and a 250-Hz lingual vibrotactile stimulus were obtained for two groups of subjects. Group 1 adjusted the vibrotactile stimulus to match the auditory stimulus, and Group 2 adjusted the auditory stimulus to match the vibrotactile stimulus. Stimulus-pulse durations and interstimulus intervals were varied over six experimental conditions for both groups. The variations in stimulus-pulse durations and interstimulus intervals had no appreciable effect on mean matching-function exponents for the two groups. A possible regression effect consistent with data from other psychophysical scaling studies was noted for matching functions of the two stimuli.     

The auditory redundant signals effect: An influence of number of stimuli or number of percepts?

In two experiments, we examined simple reaction times (RTs) for detection of the onsets and offsets of auditory stimuli. Both experiments assessed the redundant signals effect (RSE), which is traditionally defined as the reduction in RT associated with the presentation of two redundant stimuli, rather than a single stimulus. In Experiment 1, with two identical tones presented via headphones to the left ear, right ear, or both, no RSE was found in responding to tone onsets, but a large RSE was found in responding to their offsets. In Experiment 2, with a pure tone and white noise as the two stimulus alternatives, RSEs were found for responding to both onsets and offsets. The results support the notion that the occurrence of an RSE depends on the number of percepts, rather than the number of stimuli, and on the requirement to respond to stimulus onsets versus offsets. The parallel grains model (Miller & Ulrich, 2003) provides one possible account of this pattern of results.     

Repetition priming in an auditory lexical decision task: Effects of lexical status

The effect of lexical status on the time course of repetition priming was examined in an auditory lexical decision task. Words and nonwords were repeated at lags of 0, 1, 4, and 8 items (Experiment 1A) and 0, 2, 4, and 8 items (Experiment 1B). The pattern of repetition effects differed for words and nonwords in that repetition priming for nonwords at lag 0 was significantly greater than for words. The magnitude of this effect decreased when one or more items intervened. A second experiment, replicating Experiment 1A with visual presentation, clarified that the greater magnitude of repetition priming for nonwords at lag 0 is unique to the auditory modality. This finding suggests that in the course of forming a stable perceptual representation, the details of the acoustic/phonological information of an auditory stimulus are more readily available for nonwords than for words. The capacity to carry this phonological information is limited, however, and can only be maintained until another stimulus is encountered.