Intertrial interval as a contextual stimulus: Further analysis of a novel asymmetry in temporal discrimination learning.

Four experiments investigated discrimination learning when the duration of the intertrial interval (ITI) signaled whether or not the next conditional stimulus (CS) would be paired with food pellets. Rats received presentations of a 10-s CS separated half the time by long ITIs and half the time by short ITIs. When the long ITI signaled that the CS would be reinforced and the short interval signaled that it would not be (Long+/Short?), rats learned the discrimination readily. However, when the short ITI signaled that the CS would be reinforced and the long interval signaled that it would not (Short+/Long?), discrimination learning was much slower. Experiment 1 compared Long+/Short? and Short+/Long? discrimination learning with 16-min/4-min or 4-min/1-min ITI combinations. Experiment 2 found no evidence that Short+/Long? learning is inferior because the temporal cue corresponding to the short interval is ambiguous. Experiment 3 found no evidence that Short+/Long? learning is poor because the end of a long ITI signals a substantial reduction in delay to the next reinforcer. Long+/Short? learning may be faster than Short+/Long?because elapsing time involves exposure to a sequence of hypothetical stimulus elements (e.g., A then B), and feature-positive discriminations (AB+/A?) are learned quicker than feature-negative discriminations (A+/AB?). Consistent with this view, Experiment 4 found a robust feature-positive effect when sequentially presented CSs played the role of elements A and B. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Changes in the perceived duration of a narrowband sound induced by a preceding stimulus.

The authors show that a narrowband noise (NBN) is perceived as longer when presented immediately after a wideband noise (WBN), compared to when the WBN is absent. This effect depended on the WBN’s frequency spectrum overlapping that of the NBN, and it increased as the duration of the WBN increased up to 300 ms. It decreased when a silent gap was introduced between the WBN and NBN, but remained significant for an easily detectable gap of 40 ms. A correlate of the effect was observed in the mismatch negativity (MMN) to a deviant stimulus, consisting of a WBN + NBN, presented in a sequence of more common isolated WBNs. The MMN latency was longer for an on-frequency than for an off-frequency WBN; and, more importantly, the size of this difference correlated across participants with the difference in perceived duration. A rhythm-adjustment experiment showed that the presence of an on-frequency WBN immediately preceding a tone caused that tone to be heard as starting earlier than when the WBN was absent. The results are discussed in relation to the continuity illusion and models of duration encoding. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Differential effects of training intertrial interval on acquisition of trace and long-delay fear conditioning in rats.

Many factors govern conditioning effectiveness, including the intertrial interval (ITI) used during training. The present study systematically varied the training ITI during both trace and long-delay fear conditioning. Rats were trained using one of six different ITIs and subsequently tested for conditioning to the white noise conditioned stimulus (CS) and the training context. After trace conditioning, percent freezing to the CS was positively correlated with training ITI, whereas percent freezing to the context was negatively correlated with training ITI. In contrast, when rats were trained using a long-delay paradigm, freezing during the CS test session did not vary as a function of training ITI; rats exhibited robust freezing at all ITIs. The long-delay conditioned rats exhibited relatively low levels of freezing during the context test. Thus, trace is more sensitive than long-delay fear conditioning to variations in the training ITI. These data suggest that training ITI is an important variable to consider when evaluating age or treatment effects, where the optimal ITI may vary with advancing age or pharmacological treatment. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Is level irrelevant in "irrelevant speech"? Effects of loudness, signal-to-noise ratio, and binaural unmasking

A series of experiments explored the role of level, signal-to-noise ratio, and the masking-level difference in the irrelevant speech effect (ISE). In Experiment 1 the detrimental effects of irrelevant sound on serial recall were found to be the same whether the material (speech or music) was presented at a high (75 dB[A]) or low (60 dB[A]) overall level. In Experiment 2, adding pink noise to the speech signal produced a linear improvement in performance with decreasing speech-to-noise ratios. In Experiment 3 the contribution of binaural unmasking to the ISE was found to be negligible. The results (a) confirm that the segmented, changing nature of the irrelevant sound is crucial in producing the ISE and (b) suggest that the adverse effects of disruptive auditory input may be alleviated by introducing additional uniform masking noise.     

Detection of silent intervals between noises activating different perceptual channels: some properties of "central" auditory gap detection

This article describes four experiments on gap detection by normal listeners, with the general goal being to examine the consequences of using noises in different perceptual channels to delimit a silent temporal gap to be detected. In experiment 1, subjects were presented with pairs of narrow-band noise sequences. The leading element in each pair had a center frequency of 2 kHz and the trailing element's center frequency was parametrically varied. Gap detection thresholds became increasingly poor, sometimes by up to an order of magnitude, as the spectral disparity was increased between the noise bursts that marked the gap. These data suggested that gap-detection performance is impoverished when the underlying perceptual timing operation requires a comparison of activity in different perceptual channels rather than a discontinuity detection within a given channel. In experiment 2, we assessed the effect of leading-element duration in within-channel and between-channel gap detection tasks. Gap detection thresholds rose when the duration of the leading element was less than about 30 ms, but only in the between-channel case. In experiment 3, the gap-detection stimulus was redesigned so that we could probe the perceptual mechanisms that might be involved in stop consonant discrimination. The leading element was a wideband noise burst, and the trailing element was a 300-ms bandpassed noise centered on 1.0 kHz. The independent variable was the duration of the leading element, and the dependent variable was the smallest detectable gap between the elements. When the leading element was short in duration (5-10 ms), gap thresholds were close to 30 ms, which is close to the voice onset time that parses some voiced from unvoiced stop consonants. In experiment 4, the generality of the leading-element duration effect in between-channel gap detection was examined. Spectrally identical noises defining the leading and trailing edges of the gap were presented to the same or to different ears. There was a leading-element duration effect only for the between channel case. The mean gap threshold was again close to 30 ms for short leading-element durations. Taken together, the data suggest that gap detection requiring a temporal correlation of activity in different perceptual channels is a fundamentally different task to the discontinuity detection used to execute gap detection performance in the traditional, within-channel paradigm.     

Temporal integration at 6 kHz as a function of masker bandwidth

Thresholds were measured for a 6-kHz sinusoidal signal presented within a 500-ms masker. The masker was either a bandpass Gaussian noise of varying bandwidth, or a sinusoid of the same frequency as the signal. The spectrum level of the noise masker was kept constant at 20 dB SPL, and the level of the sinusoidal masker was 40 dB SPL. Thresholds for signal durations between 2 and 300 ms were measured for masker bandwidths ranging from 60 to 12,000 Hz. The masker was spectrally centered around 6 kHz. For masker bandwidths less than 600 Hz, the slope of the temporal integration function decreased with decreasing masker bandwidth. The results are not consistent with current models of temporal integration or temporal resolution. It is suggested that the results at narrow bandwidths can be understood in terms of changes in the power spectrum of the stimulus envelope or modulation spectrum. According to this view, the onset and offset ramps of the signal introduce detectable high-frequency components into the modulation spectrum, which provide a salient cue in narrowband maskers. For broadband maskers, these high-frequency components are masked by the inherent rapid fluctuations in the masker envelope. Additionally, for signal durations between 7 and 80 ms, signal thresholds decreased by up to 5 dB as the masker bandwidth increased from 1200 to 12,000 Hz. The mechanisms underlying this effect are not yet fully understood.     

Duration of signals for intertrial reinforcement and nonreinforcement in random control procedures.

In the random control procedure, responding to a conditioned stimulus (target CS) is prevented when the probability of unsignaled, unconditioned stimuli (UCS) in the intertrial interval (ITI) is equal to the probability of the UCS in the presence of the target CS. Three experiments used an autoshaping procedure with White Carneaux pigeons to examine the effects of the temporal duration of signals for the ITI UCS (cover CSs) and for concomitant periods of nonreinforcement. In Experiment 1, a short duration cover, but not a long duration cover, resulted in responding to the target CS. In Experiment 2, an explicit CS– cue during periods of nonreinforcement did not affect target acquisition. In Experiment 3, a long CS–, but not a short cover CS, was a sufficient condition for the acquisition of responding to the target CS. These results imply that the acquisition of responding to a target CS requires a discriminable period of nonreinforcement that is long relative to the target CS duration. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Time course of forward masking tuning curves in cat primary auditory cortex

Nonsimultaneous two-tone interactions were studied in the primary auditory cortex of anesthetized cats. Poststimulatory effects of pure tone bursts (masker) on the evoked activity of a fixed tone burst (probe) were investigated. The temporal interval from masker onset to probe onset (stimulus onset asynchrony), masker frequency, and intensity were parametrically varied. For all of the 53 single units and 58 multiple-unit clusters, the neural activity of the probe signal was either inhibited, facilitated, and/or delayed by a limited set of masker stimuli. The stimulus range from which forward inhibition of the probe was induced typically was centered at and had approximately the size of the neuron's excitatory receptive field. This "masking tuning curve" was usually V shaped, i.e., the frequency range of inhibiting masker stimuli increased with the masker intensity. Forward inhibition was induced at the shortest stimulus onset asynchrony between masker and probe. With longer stimulus onset asynchronies, the frequency range of inhibiting maskers gradually became smaller. Recovery from forward inhibition occurred first at the lower- and higher-frequency borders of the masking tuning curve and lasted the longest for frequencies close to the neuron's characteristic frequency. The maximal duration of forward inhibition was measured as the longest period over which reduction of probe responses was observed. It was in the range of 53-430 ms, with an average of 143 +/- 71 (SD) ms. Amount, duration and type of forward inhibition were weakly but significantly correlated with "static" neural receptive field properties like characteristic frequency, bandwidth, and latency. For the majority of neurons, the minimal inhibitory masker intensity increased when the stimulus onset asynchrony became longer. In most cases the highest masker intensities induced the longest forward inhibition. A significant number of neurons, however, exhibited longest periods of inhibition after maskers of intermediate intensity. The results show that the ability of cortical cells to respond with an excitatory activity depends on the temporal stimulus context. Neurons can follow higher repetition rates of stimulus sequences when successive stimuli differ in their spectral content. The differential sensitivity to temporal sound sequences within the receptive field of cortical cells as well as across different cells could contribute to the neural processing of temporally structured stimuli like speech and animal vocalizations.     

Variability in isochronous tapping: Higher order dependencies as a function of intertap interval.

Isochronous serial interval production (ISIP) data, as from unpaced finger tapping, exhibit higher order dependencies (drift). This fact has largely been ignored by the timing literature, one reason probably being that influential timing models assume random variability. Men and women, 22–36 years old, performed a synchronization–continuation task with intertap intervals (ITI) from 0.4 s to 2.2 s. ISIP variability was partitioned into components attributable to drift and 1st-order serial correlation, and the results indicate that (a) drift contributes substantially to the dispersion for longer ITIs, (b) drift and 1st-order correlation are different functions of the ITI, and (c) drift exhibits break close to 1.0 s and 1.4 s ITI. These breaks correspond to qualitative changes in performance for other temporal tasks, which suggests common timing processes across modalities and tasks. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Using context to resolve temporal ambiguity.

Three conditioned lick suppression experiments with rats examined the role of the context in the selection and integration of independently acquired interval relationships. In Experiment 1, rats were exposed to separate conditioned stimuli 1 and 2 (CS1–CS2) pairings with 2 different interval relationships, each in its own distinctive context, X or Y. The resultant integration was determined by the training context (X or Y) in which unconditioned stimulus (US)–CS2 backward pairings occurred, as assessed in a third neutral context (Z). In Experiment 2, rats experienced CS1–CS2 pairings with 2 different interval relationships as in Experiment 1, and then received US–CS2 pairings in both contexts X and Y. The testing context (i.e., X or Y) determined the resultant integration. In Experiment 3, rats were exposed to CS1–CS2 pairings in 2 different interval relationships each in different phases (i.e., Phases 1 and 2), and then in Phase 3 received US–CS2 pairings. The temporal context of testing (i.e., short or long retention interval) determined the resultant integration. Thus, both physical and temporal context can be used to disambiguate conflicting temporal information. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Backward inhibitory conditioning with signaled and unsignaled unconditioned stimuli: Distribution of trials across days and intertrial interval.

Through summation tests in conditioned suppression with rats we assessed the effects of distribution of trials across days (Experiment 1) and intertrial interval (ITI) (Experiment 2) on the degree of backward conditioned inhibition established through signaled and unsignaled unconditioned stimuli (USs). Two backward conditioned inhibitory stimuli (CS-s) were established within subjects: One backward CS- followed signaled shocks; the other followed unsignaled shocks. After 12 daily sessions (Experiment 1), the signaled backward CS- was strongly inhibitory and significantly more inhibitory than the unsignaled backward CS-. When the same number of trials occurred in a single long session, performances to both CS-s converged at moderate levels. At the 90-s ITI, (Experiment 2) the signaled and unsignaled backward CS-s were nearly equivalent in effectiveness. When the ITI was 540 s, performances diverged, and signaled backward CS- was substantially more effective; the longer ITI facilitated inhibitory backward conditioning based upon signaled USs but prevented the development of inhibitory backward conditioning based upon unsignaled USs. These functionally opposite effects on backward conditioned inhibition, depending on whether the US was signaled or not, are anticipated by Wagner's "standard operating procedure" (SOP) model of short-term memory. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Some observations of the effects of intertrial interval and delay on delayed matching to sample in pigeons.

Accuracy of delayed matching to sample was studied in 12 Silver King pigeons at different combinations of length of intertrial interval (ITI) and length of delay. When ITI and delay were varied between sessions in Exps I and II, accuracy increased monotonically with ITI and decreased monotonically with delay. Evidence was found for constancy of performance at equivalent ratios of ITI to delay, and percentage of correct choices was linearly related to the log of this ratio. In Exps III and IV, ITI was manipulated as a within-sessions variable. In contrast to the effect of this variable when manipulated between sessions, accuracy improved only from the shortest interval to the next shortest interval and remained constant at all longer intervals. In Exp IV, it was found that performance improved as a direct function of the mean ITI for sessions and that this relation was not affected by the degree of ITI variability within sessions. Findings resemble the effects of temporal variables on autoshaping, and the possibility that some common processes are involved in delayed matching and autoshaping is discussed. (28 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Temporal integration in face perception: Evidence of configural processing of temporally separated face parts.

Temporal integration is the process by which temporally separated visual components are combined into a unified representation. Although this process has been studied in object recognition, little is known about temporal integration in face perception and recognition. In the present study, the authors investigated the characteristics and time boundaries of facial temporal integration. Whole faces of nonfamous and famous people were segmented horizontally into 3 parts and presented in sequence, with varying interval lengths between parts. Inversion and misalignment effects were found at short intervals (0-200 ms). Moreover, their magnitude was comparable to those found with whole-face presentations. These effects were eliminated, or substantially reduced, when the delay interval was 700 ms. Order of parts presentation did not influence the pattern of inversion effects obtained within each temporal delay condition. These results demonstrate that temporal integration of faces occurs in a temporary and limited visual buffer. Moreover, they indicate that only integrated faces can undergo configural processing. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Female voice communications in high levels of aircraft cockpit noises--Part I: spectra, levels, and microphones

HYPOTHESIS: Female produced speech, although more intelligible than male speech in some noise spectra, may be more vulnerable to degradation by high levels of some military aircraft cockpit noises. The acoustic features of female speech are higher in frequency, lower in power, and appear more susceptible than male speech to masking by some of these military noises. Current military aircraft voice communication systems were optimized for the male voice and may not adequately accommodate the female voice in these high level noises. METHODS: This applied study investigated the intelligibility of female and male speech produced in the noise spectra of four military aircraft cockpits at levels ranging from 95 dB to 115 dB. The experimental subjects used standard flight helmets and headsets, noise-canceling microphones, and military aircraft voice communications systems during the measurements. RESULTS: The intelligibility of female speech was lower than that of male speech for all experimental conditions; however, differences were small and insignificant except at the highest levels of the cockpit noises. Intelligibility for both genders varied with aircraft noise spectrum and level. Speech intelligibility of both genders was acceptable during normal cruise noises of all four aircraft, but improvements are required in the higher levels of noise created during aircraft maximum operating conditions. CONCLUSIONS: The intelligibility of female speech was unacceptable at the highest measured noise level of 115 dB and may constitute a problem for other military aviators. The intelligibility degradation due to the noise can be neutralized by use of an available, improved noise-canceling microphone, by the application of current active noise reduction technology to the personal communication equipment, and by the development of a voice communications system to accommodate the speech produced by both female and male aviators.     

Temporal Ventriloquism: Sound Modulates the Flash-Lag Effect.

Asound presented in close temporal proximity to a visual stimulus can alter the perceived temporal dimensions of the visual stimulus (temporal ventriloquism). In this article, the authors demonstrate temporal ventriloquism in the flash-lag effect (FLE), a visual illusion in which a flash appears to lag relative to a moving object. In Experiment 1, the magnitude and the variability of the FLE were reduced, relative to a silent condition, when a noise burst was synchronized with the flash. In Experiment 2, the sound was presented before, at, or after the flash (± ～100 ms), and the size of the FLE varied linearly with the delay of the sound. These findings demonstrate that an isolated sound can sharpen the temporal boundaries of a flash and attract its temporal occurrence. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Perception and production of temporal intervals across a range of durations: Evidence for a common timing mechanism.

Study participants performed time perception and production tasks over a set of 4 intervals ranging from 325 to 550 ms. In 3 experiments, variability on both the production and perception tasks was found to be linearly related to the square of the target intervals. If the perception and production of short temporal intervals use a common timing mechanism, the slopes of the functions for the 2 tasks should be identical. The results of Experiment 1 failed to support this prediction. However, when the 2 tasks were made more similar by providing a single (Experiment 2) or multiple (Experiment 3) presentations of the target interval per judgment or production, the perception and production functions were nearly identical. The results suggest that temporal judgments and productions are based on an integrated internal representation of the target interval rather than reference to an internal oscillatory process. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of bilateral auditory cortical lesions on gap-detection thresholds in the ferret (Mustela putorius).

Ferrets were tested for their ability to detect temporal gaps in noise before and after bilateral lesions of the primary auditory cortex. Thresholds for gap detection were determined first for normal animals with band-pass noises at various center frequencies (0.5 to 32 kHz) and at 8 kHz with various sound pressure levels (-10 to 70 dB). Gap-detection ability improved steadily as sound pressure increased up to 70 dB. No systematic relation was found between threshold and center frequency. To determine the effects of brain damage, ferrets were tested with 8-kHz band-pass noise at 70 dBSPL. After bilateral lesions of auditory cortex, ferrets were still capable of detecting gaps, but the mean threshold was elevated from 10.1 to 20.1 ms. The data demonstrate that auditory cortex is important for perceptual tasks requiring fine temporal resolution. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Benefits of linear amplification and multichannel compression for speech comprehension in backgrounds with spectral and temporal dips

People with cochlear hearing loss have markedly higher speech-receptions thresholds (SRTs) than normal for speech presented in background sounds with spectral and/or temporal dips. This article examines the extent to which SRTs can be improved by linear amplification with appropriate frequency-response shaping, and by fast-acting wide-dynamic-range compression amplification with one, two, four, or eight channels. Eighteen elderly subjects with moderate to severe hearing loss were tested. SRTs for sentences were measured for four background sounds, presented at a nominal level (prior to amplification) of 65 dB SPL: (1) A single female talker, digitally filtered so that the long-term average spectrum matched that of the target speech; (2) a noise with the same average spectrum as the target speech, but with the temporal envelope of the single talker; (3) a noise with the same overall spectral shape as the target speech, but filtered so as to have 4 equivalent-rectangular-bandwidth (ERB) wide spectral notches at several frequencies; (4) a noise with both spectral and temporal dips obtained by applying the temporal envelope of a single talker to speech-shaped noise [as in (2)] and then filtering that noise [as in (3)]. Mean SRTs were 5-6 dB lower (better) in all of the conditions with amplification than for unaided listening. SRTs were significantly lower for the systems with one-, four-, and eight-channel compression than for linear amplification, although the benefit, averaged across subjects, was typically only 0.5 to 0.9 dB. The lowest mean SRT (-9.9 dB, expressed as a speech-to-background ratio) was obtained for noise (4) and the system with eight-channel compression. This is about 6 dB worse than for elderly subjects with near-normal hearing, when tested without amplification. It is concluded that amplification, and especially fast-acting compression amplification, can improve the ability to understand speech in background sounds with spectral and temporal dips, but it does not restore performance to normal.     

Infant perception of audio-visual speech synchrony.

Three experiments investigated perception of audio-visual (A-V) speech synchrony in 4- to 10-month-old infants. Experiments 1 and 2 used a convergent-operations approach by habituating infants to an audiovisually synchronous syllable (Experiment 1) and then testing for detection of increasing degrees of A-V asynchrony (366, 500, and 666 ms) or by habituating infants to a detectably asynchronous syllable (666 ms; Experiment 2) and then testing for detection of decreasing degrees of asynchrony (500, 366, and 0 ms). Following habituation to the synchronous syllable, infants detected only the largest A-V asynchrony (0 ms vs. 666 ms), whereas following habituation to the asynchronous syllable, infants detected the largest asynchrony (666 ms vs. 0 ms) as well as a smaller one (666 ms vs. 366 ms). Experiment 3 investigated the underlying mechanism of A-V asynchrony detection and indicated that responsiveness was based on a sensitivity to stimulus-energy onsets rather than the dynamic correlation between acoustic and visible utterance attributes. These findings demonstrated that infant perception of A-V speech synchrony is subject to the effects of short-term experience and that it is driven by a low-level, domain-general mechanism. (PsycINFO Database Record (c) 2010 APA, all rights reserved)