Amplitude discrimination of sinusoids and narrow-band noise with Rayleigh properties

The ability of human observers to discriminate differences in the amplitude of sinusoids and narrow-band noises was measured by the rating method of detection theory. Although each sinusoid (always 1000 Hz) was presented at a fixed amplitude, its amplitude on any trial was drawn from one of two Rayleigh probability distributions that differed in mean amplitude: a signal distribution and a noise distribution. Similarly, the amplitudes of the narrow-band noises were distributed as the Rayleigh distribution by virtue of the reciprocal relation between their bandwidth (100 Hz centered on 1000 Hz) and duration (10 msec). The obtained psychometric functions showing the area under the ROC as a function of signal-to-noise ratio were similar for both kinds of signals and were displaced, on average, about 4 dB from an ideal observer’s function. The slopes of the obtained functions were similar to those of an ideal observer using 1 degree of freedom—half the number available in Rayleigh noise.     

Amplitude discrimination of sinusoids and narrow-band noise with Rayleigh properties.

The ability of human observers to discriminate differences in the amplitude of sinusoids and narrow-band noises was measured by the rating method of detection theory. Although each sinusoid (always 1000 Hz) was presented at a fixed amplitude, its amplitude on any trial was drawn from one of two Rayleigh probability distributions that differed in mean amplitude: a signal distribution and a noise distribution. Similarly, the amplitudes of the narrow-band noises were distributed as the Rayleigh distribution by virtue of the reciprocal relation between their bandwidth (100 Hz centered on 1000 Hz) and duration (10 msec). The obtained psychometric functions showing the area under the ROC as a function of signal-to-noise ratio were similar for both kinds of signals and were displaced, on average, about 4 dB from an ideal observer's function. The slopes of the obtained functions were similar to those of an ideal observer using 1 degree of freedom--half the number available in Rayleigh noise.     

Psychometric functions for the discrimination of differences in intensity of gaussian noise

A new theory of sensory functioning by Laming predicts how the shape of the psychometric function depends on the context in which a signal is presented. The discrimination of intensities of noise was therefore studied with four different stimulus configurations. In one, observers discriminated between two separate noise samples that differed in intensity. In accordance with the theory, a normal probability integral provided a better fit to each observer's data than either of two other functions: a normal integral with respect to the square of the difference, or a normal integral with respect to the fourth power of the difference. In a second task, observers detected an increment in a continuous noise. For eight out of nine sets of data, a square-law function provided a better fit than either a normal integral or fourth-power function. A third task asked observers to decide which of two noises was amplitude modulated. The predicted square-law function provided the best fit for four out of five observers. In a fourth task, one observer detected an interval of amplitude modulation in a continuous noise. As predicted by the theory, a fourth-power function provided the best fit. In addition, Weber fractions for difference discriminations decreased approximately with the square root of sample duration for durations up to 300 msec, whereas Weber fractions for increment detections decreased approximately directly with duration for durations up to 100 msec. The results are usually in qualitative agreement with the theory and often in quantitative agreement as well.     

Temporal processing capabilities in repetition conduction aphasia

This study investigates the temporal resolution capacities of the central-auditory system in a subject (NP) suffering from repetition conduction aphasia. More specifically, the patient was asked to detect brief gaps between two stretches of broadband noise (gap detection task) and to evaluate the duration of two biphasic (WN-3) continuous noise elements, starting with white noise (WN) followed by 3 kHz bandpass-filtered noise (duration discrimination task). During the gap detection task, the two portions of each stimulus were either identical (“intra-channel condition”) or differed (“inter-channel condition”) in the spectral characteristics of the leading and trailing acoustic segments. NP did not exhibit any deficits in the intra-channel condition of the gap detection task, indicating intact auditory temporal resolution across intervals of 1–3 ms. By contrast, the inter-channel condition yielded increased threshold values. Based upon the “multiple-looks” model of central-auditory processing, this profile points at a defective integration window operating across a few tens of milliseconds – a temporal range associated with critical features of the acoustic speech signal such as voice onset time and formant transitions. Additionally, NP was found impaired during a duration discrimination task addressing longer integration windows (ca. 150 ms). Concerning speech, this latter time domain approximately corresponds to the duration of stationary segmental units such as fricatives and long vowels. On the basis of our results we suggest, that the patient’s auditory timing deficits in non-speech tasks may account, at least partially, for his impairments in speech processing.     

The effects of marker-related temporal cues on auditory gap-duration discrimination

In three experiments, we examined the ability of listeners to discriminate the duration of temporal gaps (silent intervals) and the influence of other temporal stimulus properties on their performance. In the first experiment, gap-duration discrimination thresholds were measured either in continuous noise or with noise markers with durations of 3 and 300 ms. Thresholds measured with 300-ms markers differed from those measured in continuous noise or with 3-ms markers. In the second experiment, stimuli consisting of a gap between two discrete markers were generated such that the gap duration, the onset-to-onset duration between markers, and the duration of the first marker were pseudorandomized across trials. Listeners’ responses generally were consistent with the cue that was identified as the target cue from among the three cues in each block of trials, but the data suggested that the onset-to-onset cue was particularly salient in all conditions. Using a modified method-of-adjustment procedure in the third experiment, subjects were instructed to discriminate between the durations of gaps in discrete markers of different durations in two intervals, where the gap duration in one interval was adapted to measure the point of subjective equality. Without feedback, listeners tended to equate the onset-to-onset times of the markers rather than the gap durations. Overall, the results indicated that listeners’ judgments of silent gaps between two discrete markers are strongly influenced by the onset-to-onset time, or rhythm, of the markers.     

Frequency-shift detectors bind binaural as well as monaural frequency representations

Previous psychophysical work provided evidence for the existence of automatic frequency-shift detectors (FSDs) that establish perceptual links between successive sounds. In this study, we investigated the characteristics of the FSDs with respect to the binaural system. Listeners were presented with sound sequences consisting of a chord of pure tones followed by a single test tone. Two tasks were performed. In the "present/absent" task, the test tone was either identical to one of the chord components or positioned halfway in frequency between two components, and listeners had to discriminate between these two possibilities. In the "up/down" task, the test tone was slightly different in frequency from one of the chord components and listeners had to identify the direction (up or down) of the corresponding shift. When the test tone was a pure tone presented monaurally, either to the same ear as the chord or to the opposite ear, listeners performed the up/down task better than the present/absent task. This paradoxical advantage for directional frequency shifts, providing evidence for FSDs, persisted when the test tone was replaced by a dichotic stimulus consisting of noise but evoking a pitch sensation as a consequence of binaural processing. Performance in the up/down task was similar for the dichotic stimulus and for a monaural narrow-band noise matched in pitch salience to it. Our results indicate that the FSDs are insensitive to sound localization mechanisms and operate on central frequency representations, at or above the level of convergence of the monaural auditory pathways.     

Segregated in perception,integrated for action: Immunity of rhythmic sensorimotor coordination to auditory stream segregation

Auditory stream segregation can occur when tones of different pitch (A, B) are repeated cyclically: The larger the pitch separation and the faster the tempo, the more likely perception of two separate streams is to occur. The present study assessed stream segregation in perceptual and sensorimotor tasks, using identical ABBABB … sequences. The perceptual task required detection of single phase-shifted A tones; this was expected to be facilitated by the presence of B tones unless segregation occurred. The sensorimotor task required tapping in synchrony with the A tones; here the phase correction response (PCR) to shifted A tones was expected to be inhibited by B tones unless segregation occurred. Two sequence tempi and three pitch separations (2, 10, and 48 semitones) were used with musically trained participants. Facilitation of perception occurred only at the smallest pitch separation, whereas the PCR was reduced equally at all separations. These results indicate that auditory action control is immune to perceptual stream segregation, at least in musicians. This may help musicians coordinate with diverse instruments in ensemble playing.     

Minds on the blink: The relationship between inattentional blindness and attentional blink

Failures of conscious visual awareness occur when specific task demands prevent an observer from detecting a stimulus that would otherwise be clearly visible. Two examples are inattentional blindness (IB) and attentional blink (AB). IB is the failure to detect an unexpected stimulus when attention is otherwise engaged. AB describes the inability to detect a second target that is presented within 180-500?ms of the first target. Previous research has suggested that similar cognitive processes underlie both IB and AB; however, they are distinct phenomena, and no evidence has directly linked the two. We tested the same group of observers on an IB task and an AB task. Consistent with our hypotheses, we found that "non-noticers" who failed to detect an unexpected stimulus in the IB task also demonstrated a larger AB effect. This suggests that some observers may be more generally susceptible to failures of conscious visual awareness, regardless of specific context.     

Target duration effects on iconic memory: the confounding role of changing stimulus dimensions

Observers' accuracy in detecting a narrow spatial gap between two brief, luminous rectangles presented successively was determined within a two-alternative, forced-choice procedure. This successive-field task requires iconic memory, because the information (rectangle position) in the two presentations must be combined for successful gap detection. On this task, the effect of varying the duration of the first rectangle was systematically investigated over several target luminance levels and for several ISI conditions between rectangles. At the long ISI conditions (100 and 300 ms), the effects of increasing stimulus duration was to improve performance. However, at the brief ISI condition (20 ms), increasing stimulus duration initially depressed task performance. It was found that, with practice, this initial performance drop largely disappeared, and the beneficial influence of increasing target duration was again obtained. These results are discussed in terms of (a) a proposed retinal locus for the iconic memory involved and (b), at a more general level, the potentially distracting role of changing stimulus dimensions on a task employing transient stimuli as in the present study.     

On the relation between roll and pitch

Studies have found that rolling the visual environment affects observers' perception of gravitational vertical and horizontal and that pitching the environment affects observers' perception of pitch. However, the relationship between these two perceptions is not fully understood. In the present work, observers performed three tasks while in a visual surround whose pitch and roll was manipulated. In the first task, observers adjusted a rod in the frontal-parallel plane to the horizontal (roll). In a second task, they adjusted a rod along a plane parallel to straight-ahead to the vertical (pitch). In the final task (“in-between”), they adjusted a rod midway between the first two conditions. The typical pitch and roll effects were found, as well as a contribution of both pitch and roll to the in-between task. No interaction between pitch and roll effects was found, indicating independent cognitive representations.     

Ambiguity and the 'mental eye' in pictorial relief

Photographs of scenes do not determine scenes in the sense that infinitely many different scenes could have given rise to any given photograph. In psychophysical experiments, observers have (at least partially) to resolve these ambiguities. The ambiguities also allow them to vary their response within the space of 'veridical' responses. Such variations may well be called 'the beholder's share' since they do not depend causally on the available depth cues. We determined the pictorial relief for four observers, four stimuli, and four different tasks. In all cases we addressed issues of reliability (scatter on repeated trials) and consistency (how well the data can be explained via a smooth surface, any surface). All data were converted to depth maps which allows us to compare the relief from the different operationalisations. As expected, pictorial relief can differ greatly either between observers (same stimulus, same task) or between operationalisations (same observer, same stimulus). However, when we factor out the essential ambiguity, these differences almost completely vanish and excellent agreement over tasks and observers pertains. Thus, observers often resolve the ambiguity in idiosyncratic ways, but mutually agree--even over tasks--in so far as their responses are causally dependent on the depth cues. A change of task often induces a change in 'mental perspective'. In such cases, the observers switch the 'beholder's share', which resolves the essential ambiguity through a change in viewpoint of their 'mental eye'.     

Noise annoyance during the performance of different nonauditory tasks

Three experiments were performed to study the effects of an ongoing task on the annoyance response to noise. In the first two experiments a total of five tasks were used: three versions of a proofreading task, a finger-dexterity task, and a complex reaction time (RT) task. Subjects performed the tasks during exposure to two levels of a continuous broadband noise. Task was of no consequence for rated annoyance. Four tasks were used in Experiment 3: proofreading, complex RT, grammatical reasoning, and simple RT. A third type of noise, irrelevant speech, was added to the broadband noises. Rated annoyance was lower during simple RT than during the reasoning and proofreading tasks, especially in the irrelevant speech condition. The difference corresponded to a 6-dB difference in noise level. It was concluded that task differences probably only explain a small part of the widely differing noise tolerance levels at different work places.     

Task demands determine the specificity of the search template

When searching for an object, an observer holds a representation of the target in mind while scanning the scene. If the observer repeats the search, performance may become more efficient as the observer hones this target representation, or "search template," to match the specific demands of the search task. An effective search template must have two characteristics: It must reliably discriminate the target from the distractors, and it must tolerate variability in the appearance of the target. The present experiment examined how the tolerance of the search template is affected by the search task. Two groups of 18 observers trained on the same set of stimuli blocked either by target image (block-by-image group) or by target category (block-by-category group). One or two days after training, both groups were tested on a related search task. The pattern of test results revealed that the two groups of observers had developed different search templates, and that the templates of the block-by-category observers better captured the general characteristics of the category. These results demonstrate that observers match their search templates to the demands of the search task.     

On the rate of acquisition of visual information about space,time, and intensity

The temporal course of acquisition of visual information was mapped by measuring the speed and accuracy With which Ss could discriminate the position, intensity, or duration of a stimulus that was varied independently on these three binary dimensions. The speed-accuracy tradeoff was different for each of the three discrimination tasks, with performance substantially superior in the position discrimination task. In the intensity and duration discrimination tasks, there were systematic changes with RT in the relative influences of the three stimulus variables over the two alternative responses, suggesting .three phases of the corresponding perceptual processes: an initial dominance by position of the stimulus, a subsequent, joint influence by both intensity and duration, and finally an exclusive control by the correct dimension. The results demonstrate that Ss can selectively attend to various dimensions of the same stimulus, with concommitantly varying time constants. The perceptual processes being tapped by a discrimination task depend upon instructions and upon RT.     

Active control in interrupted dynamic spatial orientation: The detection of orientation change

Gibson (1966, 1979) suggested that an important property of perception is that the observer is active. Two experiments were conducted to examine the benefits of active observation in determining dynamic spatial orientation. Subjects were presented with displays simulating locomotion through a three-dimensional environment. Active observers continuously controlled locomotion, whereas passive observers viewed the display. During the trial, the display was blacked out for a brief period, followed by a static image that was at either the correct or the incorrect orientation following the blackout. Subjects were required to indicate whether they were positioned at the correct extrapolated orientation. The presence or absence of orientation change, the type of change (changes in rotation about the depth axis [roll], horizontal axis [pitch], or forward translation), the duration of the blackout, and the consistency of change were varied. In addition, the experiments used either a compensatory or a pursuit tracking task. Active observers had greater sensitivity than did passive observers in detecting a change for both tracking tasks. Subjects in both experiments exhibited greater sensitivity in detecting inconsistent changes (relative to consistent changes), suggesting that the dynamics specified by optical flow were incorporated in extrapolated orientation. In addition, sensitivity decreased with an increase in blackout duration. The results are discussed in terms of an extrapolation model of perception that incorporates the responses executed by active observers.     

Perceptual encoding and decision strategies for integral dimensions

These three experiments employed rectangles in stimulus identification tasks. Consistent with the stimulus set used by Weintraub, the rectangles were generated by modifying a square. Across experiments, the number of stimulus/response alternatives was varied (two-, three-, and four-choice tasks). In the two-choice task, redundancy gain for the positively correlated set was just as large as for the negatively correlated set. In contrast, reaction time ws faster for the negatively correlated set than for the positively correlated set in the three-choice task (after extended practice) and in the four-choice task. Considered in the context of previous research, the data support two conclusions. First, the initial perceptual processing of rectangles is accomplished by separate dimensional analyzers operating in parallel. Second, observers adopt a different decision strategy for the negatively correlated set than for the positively correlated and the single dimension sets when the number of stimulus/response alternatives is increased.     

Tracking the first two seconds: three stages of visual information processing?

We compared visual priming and comparison tasks to assess information processing of a stimulus during the first 2 s after its onset. In both tasks, a 13-ms prime was followed at varying SOAs by a 40-ms probe. In the priming task, observers identified the probe as rapidly and accurately as possible; in the comparison task, observers determined as rapidly and accurately as possible whether or not the probe and prime were identical. Priming effects attained a maximum at an SOA of 133 ms and then declined monotonically to zero by 700 ms, indicating reliance on relatively brief visuosensory (iconic) memory. In contrast, the comparison effects yielded a multiphasic function, showing a maximum at 0 ms followed by a minimum at 133 ms, followed in turn by a maximum at 240 ms and another minimum at 720 ms, and finally a third maximum at 1,200 ms before declining thereafter. The results indicate three stages of prime processing that we take to correspond to iconic visible persistence, iconic informational persistence, and visual working memory, with the first two used in the priming task and all three in the comparison task. These stages are related to stages presumed to underlie stimulus processing in other tasks, such as those giving rise to the attentional blink.     

Attributions for Performance on Luck and Skill Tasks: Effects of Outcome,Sex of Performer,and Sex of Subject

Attributions for and evaluations of a stimulus persons's preformance were assessed as a function of the sex of the stimulus person, sex of the observer, type of task (luck or skill), and outcomes (success or failure). An interaction between type of task and sex of stimulus person was expected, with observers expecting males to perform better than females on the skill task because of ability, and females to perform better than males on the luck task because of task ease. The results provided partial support for the predicted interaction. Task difficulty was more relevant for females on the luck task than for males. Effort was rated as more important for females than for males when the success was on the skill task. All of the ratings were influenced by the task-type manipulation.     

The Effects of Selective Cholinergic Basal Forebrain Lesions and Aging upon Expectancy in the Rat

The effects of selective cholinergic cell loss within the basal forebrain (BF) were determined using a task that requires shifting of attention between two visual stimuli. Discriminability between two stimuli and response bias were determined in young and old F-344 rats given BF injections of IgG-192 saporin (100 ng). The lesion reduced ChAT activity in the frontal and parietal cortices, hippocampus, and olfactory bulbs. The lesion did not significantly alter Na⁺/K⁺-ATPase activity in cortex, hippocampus, or olfactory bulbs, or endogenous levels of neuropeptide Y and neurokinin B within the BF. The BF lesions impaired both stimulus discriminability and response bias in young and old rats. The BF lesions had a significantly greater effect upon stimulus discriminability and response bias in aged rats, compared to young rats, only when the stimulus duration was very brief, i.e., when the task was most difficult to solve. At longer stimulus durations, aging and lesions showed no interaction. The results suggest that the selective loss of cholinergic cells in the BF, but not normal aging, impairs the ability to discriminate between independent sensory stimuli. The loss of these cells confers a response bias in simple operant tasks involving motor responses to reward-related visual stimuli.     

Effects of perceptual quality on the processing of human faces presented to the left and right cerebral hemispheres

Three experiments examined the effects of stimulus duration, retinal eccentricity, and visual noise on the processing of human faces presented to the left visual field/right hemisphere (LVF-RH) and right visual field/left hemisphere (RVF-LH). In Experiment 1 observers identified which of 10 similar male faces was presented on a screen. The single face was presented for 10, 55, or 100 ms at 1 degree, 4 degrees, or 9 degrees of visual angle to the left or right of fixation. Decreasing stimulus duration and increasing retinal eccentricity lowered face recognition. The effect of duration was the same for LVF-RH and RVF-LH trials, but the detrimental effect of increasing retinal eccentricity was larger on LVF-RH trials than on RVF-LH trials. In Experiment 2 observers indicated whether a single face from this same set was a member of a memorized set of five positive faces. The probe face on each trial was presented alone or embedded in visual noise. Visual noise increased the error rate more on LVF-RH trials than on RVF-LH trials. This effect was replicated in Experiment 3, which also required observers to make a much easier discrimination between male and female faces. In the male/female task visual noise tended to impair performance more on RVF-LH trials than on LVF-RH trials, opposite the effect for the male/male task. These results are discussed in terms of hemispheric asymmetry for global versus local features of faces, the level of feature analysis demanded by a task, and the level of feature analysis most disrupted by perceptual degradation.