Visual beats: Preliminary observations of perceived rate as a function of retinal locus stimulated

Visual beats produced by simultaneous presentation of two different flicker frequencies were used to determine the temporal processing of various retinal areas. The dichoptic presentation of two different flicker frequencies to the center and periphery of the retina resulted in a perceived beat rate that equalled the physical beat frequency. When the stimuli were presented to more discrete retinal areas (temporal vs temporal and nasal vs temporal), the perceived beat rate also equalled the physical beat frequency. The data indicate that different flicker frequencies stimulating divergent retinal loei can be represented accurately and simultaneously in the visual system: Differences in temporal resolution at the different retinal loei do not occur for this repetitive stimulation.     

Flicker adaptation in the periphery at constant perceived modulation depth

At constant physical flicker modulation depth, the time taken to adapt to flicker in the periphery varies inversely with temporal frequency. It has recently been suggested that this effect may indicate differential susceptibility to adaptation of the underlying temporal mechanisms. Using suprathreshold gratings, temporally modulated in contrast at constant perceived, rather than physical, modulation depth, we found the opposite result: the time required to adapt increased with temporal frequency. Given some uncertainty concerning the appropriateness of employing apparent or physically constant modulation depths, we conclude that rate of adaptation does not, at present, provide clear evidence as to the nature of the underlying temporal mechanisms.     

Second-order reversed phi.

In a first-order reversed-phi motion stimulus (Anstis, 1970), the black-white contrast of successive frames is reversed, and the direction of apparent motion may, under some conditions, appear to be reversed. It is demonstrated here that, for many classes of stimuli, this reversal is a mathematical property of the stimuli themselves, and the real problem is in perceiving forward motion, which involves the second- or third-order motion systems or both. Three classes of novel second-order reversed-phi stimuli (contrast, spatial frequency, and flicker modulation) that are invisible to first-order motion analysis were constructed. In these stimuli, the salient stimulus features move in the forward (feature displacement) direction, but the second-order motion energy model predicts motion in the reversed direction. In peripheral vision, for all stimulus types and all temporal frequencies, all the observers saw only the reversed-phi direction of motion. In central vision, the observers also perceived reversed motion at temporal frequencies above about 4 Hz, but they perceived movement in the forward direction at lower temporal frequencies. Since all of these stimuli are invisible to first-order motion, these results indicate that the second-order reversed-phi stimuli activate two subsequent competing motion mechanisms, both of which involve an initial stage of texture grabbing (spatiotemporal filtering, followed by fullwave rectification). The second-order motion system then applies a Reichardt detector (or equivalently, motion energy analysis) directly to this signal and arrives at the reversed-phi direction. The third-order system marks the location of features that differ from the background (the figure) in a salience map and computes motion in the forward direction from the changes in the spatiotemporal location of these marks. The second-order system's report of reversed movement dominates in peripheral vision and in central vision at higher temporal frequencies, because it has better spatial and temporal resolution than the third-order system, which has a cutoff frequency of 3-4 Hz (Lu & Sperling, 1995b). In central vision, below 3-4 Hz, the third-order system's report of resolvable forward movement of something salient (the figure) dominates the second-order system's report of texture contrast movement.     

Perceptual grouping based on temporal structure: Impact of subliminal flicker and visual transients

In two experiments we examined the perceived grouping of grids of equidistant dots, which are rapidly modulated over time so that alternate rows or columns are presented out of phase. In Experiment 1, we report that observers were able to group the grids consistent with the temporal modulation reliably, even at contrasts/frequencies for which flicker was not detectable. Moreover, flicker thresholds decreased with stimulus duration, whilst grouping thresholds did not change. In Experiment 2, we examined the impact of visual transients, by measuring performance when, either a mask or a contrast ramp was presented before and after the stimulus. Performance dropped substantially for both conditions, but remained significantly above chance. The results are discussed in relation to the role of temporal correlations in stimulus modulations and visual transients in grouping.     

Spatial and temporal frequency in figure-ground organization

Figure-ground organization of an ambiguous pattern can be manipulated by the spatial and temporal frequency content of the two regions of the pattern. Controlling for space-averaged luminance and perceived contrast, we tested patterns in which the two regions of the ambiguous pattern contained sine-wave gratings of 8, 4, 1, or 0.5 cycles per degree (cpd) undergoing on:off flicker at the rates of 0, 3.75, 7.5, or 15 Hz. For a full set of combinations of temporal frequency differences, with each spatial frequency the higher temporal frequency was seen as background for more of the viewing time. For two spatial frequency combinations, 1 and 4 cpd, and 1 and 8 cpd, tested under each of the four temporal frequencies, the lower spatial frequency region was seen as the background for more of the viewing time. When the effects of spatial and temporal frequency were set in opposition, neither was predominant in determining perceptual organization. It is suggested that figure-ground organization may parallel the sustained-transient response characteristics of the visual system.     

Second-order reversed phi

In a first-order reversed-phi motion stimulus (Anstis, 1970), the black-white contrast of successive frames is reversed, and the direction of apparent motion may, under some conditions, appear to be reversed. It is demonstrated here that, for many classes of stimuli, this reversal is a mathematical property of the stimuli themselves, and the real problem is in perceiving forward motion, which involves the second- or third-order motion systems or both. Three classes of novel second-order reversed-phi stimuli (contrast, spatial frequency, and flicker modulation) that are invisible to first-order motion analysis were constructed. In these stimuli, the salient stimulus features move in theforward (feature displacement) direction, but the second-order motion energy model predicts motion in thereversed direction. In peripheral vision, for all stimulus types and all temporal frequencies, all the observers saw only the reversed-phi direction of motion. In central vision, the observers also perceived reversed motion at temporal frequencies above about 4 Hz, but they perceived movement in the forward direction at lower temporal frequencies. Since all of these stimuli are invisible to first-order motion, these results indicate that the second-order reversed-phi stimuli activate two subsequent competing motion mech-anisms, both of which involve an initial stage of texture grabbing (spatiotemporal filtering, followed by fullwave rectification). The second-order motion system then applies a Reichardt detector (or equiva-lently, motion energy analysis) directly to this signal and arrives at the reversed-phi direction. The third-order system marks the location of features that differ from the background (the figure) in a salience map and computes motion in the forward direction from the changes in the spatiotemporal location of these marks. The second-order system’s report of reversed movement dominates in peripheral vision and in central vision at higher temporal frequencies, because it has better spatial and temporal resolu-tion than the third-order system, which has a cutoff frequency of 3–4 Hz (Lu & Sperling, 1995b). In cen-tral vision, below 3–4 Hz, the third-order system’s report of resolvable forward movement of something salient (the figure) dominates the second-order system’s report of texture contrast movement.     

Feature synchrony-asynchrony and rate of change in visual search

ABSTRACT

Attention is known to be sensitive to the temporal structure of scenes. We initially tested whether feature synchrony, an attribute with potential special status because of its association with objecthood, is something which draws attention. Search items were surrounded by colours which periodically changed either in synchrony or out-of synchrony with periodic changes in their shape. Search for a target was notably faster when the target location contained a unique synchronous feature change amongst asynchronous changes. However, the reverse situation produced no search advantage. A second experiment showed that this effect of unique synchrony was actually a consequence of the lower rate of perceived flicker in the synchronous compared to the asynchronous items, not the synchrony itself. In our displays it seems that attention is drawn towards a location which has a relatively low rate of change. Overall, the pattern of results suggested the attentional bias we find is for relative temporal stability. Results stand in contrast to other work which has found high and low flicker rates to both draw attention equally [Cass, J., Van der Burg, E., & Alais, D. (2011). Finding flicker: Critical differences in temporal frequency capture attention. Frontiers in Psychology, 2, 320]. Further work needs to determine the exact conditions under which this bias is and is not found when searching in complex dynamically-changing displays.     

Antiphase flicker induces depth segregation

We examined the influence of the temporal phase of flickering stimuli on perceptual organization. When two regions of a uniform random-dot field are flickered in temporal alternation with the same flicker rate, one of the regions appears to lie in front of the other. Within the range of temporal frequencies used in the present experiments, depth perception was maximal between 5 and 31.3 Hz. Which region of the two is perceived as lying in front is different from person to person and sometimes fluctuates within the same subject, but when two regions are of different sizes, the smaller region tends to be perceived in front for longer than the larger region. The depth segregation was not due to a luminance difference, because the average temporal luminance of the regions was kept equal. Strikingly, the illusory depth segregation is perceived even between two adjacent regions whose densities of dots, sizes, shapes, and flicker rates are identical. This result suggests that a difference of temporal phase between two flickering regions is crucial for this new depth perception.     

A new visual illusion: flickering fields are localized in a depth plane behind nonflickering fields

Flickering regions of the visual field are perceived to lie well behind regions which are not flickered. The depth segregation is not due to luminance differences since the average temporal luminance across all the regions was equal. This depth effect produced by flicker is not dependent on the texture of the visual field; nor does it depend on a specific configuration of the flickering and nonflickering areas. It is optimal at a temporal frequency around 6 Hz, which suggests that visual channels responding maximally to high temporal frequencies are involved in the segregation of perceptual regions in depth.     

On utrocular discrimination

Observers with good stereoacuity judged which eye received sine-wave grating patterns in a two-category forced-choice procedure. Large individual differences were found, but for most observers reliable discrimination was achieved at low spatial frequencies. No observer could perform the task above chance levels at high spatial frequencies. Discrimination was unaffected by retinal location, grating orientation, grating contrast, stimulus duration, or practice with feedback. Among observers who could perform the task, the following results were obtained: (1) Introduction of high spatial frequency components did not interfere with performance so long as a low spatial frequency component was present. (2) When gratings of low equal spatial frequency were presented to both eyes simultaneously at different contrast levels, observers could identify which eye received the higher contrast. (3) At low spatial frequencies, observers could distinguish monocular from binocular presentation. (4) Temporal frequency variations (counterphase flicker) influenced performance for some observers. Binocular summation and interocular transfer were unaffected by the spatial frequency variations which modulate utrocular discrimination. A new procedure for measuring stereopsis was developed which made possible comparison of utrocular discrimination with stereopsis at specific spatial frequencies. Stereopsis appeared mildly affected by spatial frequency.     

Time perception and the internal clock: Effects of visual flicker on the temporal oscillator

Abstract

Our ability to estimate time intervals has sometimes been attributed to a biological source of temporal information. A model for a temporal oscillator that provides such information has recently been described (Treisman, Faulkner, Naish & Brogan, 1990). This predicts that an imposed stimulus rhythm at certain frequencies may interfere with the temporal oscillator so as to alter its frequency. This interference would cause perturbations in temporal judgements at certain frequencies of the imposed rhythm. The pattern of interference would depend on the frequency at which the temporal oscillator runs, and so would contain information about the oscillator frequency. Evidence for such a pattern was found when auditory clicks at different rates were presented concurrently with time intervals whose durations subjects estimated. The present study examines whether a similar interference pattern can be obtained if visual flicker is substituted for auditory clicks. On each trial, flicker was presented at a rate between 2.5 and 17.5 Hz, concurrently with a time interval to be estimated. A pattern of increased estimates at some rates and decreased estimates at others was obtained. This pattern showed similarities to interference patterns obtained using auditory clicks. This provides evidence that the entrainment of the internal clock predicted by the model can also be produced by visual inputs. Other theoretical implications are discussed.     

Individual differences in pulse brightness perception

When brightness-pulse duration relations are studied with a simultaneous brightness discrimination procedure, three classes of observers emerge (Bowen & Markell, 1980). These classes are defined by whether or not observers perceive temporal brightness enhancement (the Broca-Sulzer effect) under two asynchrony conditions for pulses to be compared: simultaneous onset and simultaneous offset. Type A observers perceive brightness enhancement for both asynchrony conditions; Type B observers perceive brightness enhancement for simultaneous offset of pulses but not for simultaneous onset; Type C observers do not generate the Broca-Sulzer effect under either asynchrony condition. Here we present supplementary measures on observers of all three types: (1) magnitude estimation of the brightness of single pulses of light of varying duration, (2) modulation sensitivity for sin~wave flicker, and (3) contrast sensitivity for moving sine-wave gratings. The magnitude estimation data differentiated the three types of observers, but flicker and motion sensitivity did not. The three classes of observers probably differ in the perceptual criteria they employ in judging the brightness of isolated pulses of light; they probably do not differ in their underlying neurophysiological responses.     

Evidence for independent processing of subjective contour brightness and sharpness.

Subjective contours have been of considerable interest because of their importance to theories and physiological models of form perception. In particular, they have recently been characterized as the result of magnocellular cortical processing. There is, however, a paucity of parametric data relating to basic psychophysical parameters in this field. Two experiments are reported in which the roles of subjective contour size, retinal eccentricity, and flicker rate in subjective contour salience were investigated. Eleven observers estimated subjective contour magnitude using an Ehrenstein configuration. Configurations ranging in size from 0.25 to 3 deg were presented to three retinal loci (fovea, 2 deg, and 4 deg) at flicker rates ranging from 5 to 15 Hz. Subjective contour brightness and distinctness were measured separately. Brightness was greatest at a subjective contour size of about 1.25 deg, at flicker rates of 5-7 Hz, and at 3 deg peripheral for all flicker rates and all but the smallest stimulus sizes. Distinctness decreased with eccentricity and flicker, but remained high at small diameters (thus implicating spatially sensitive mechanisms). Taken together, the results support a magnocellular processing of subjective contours with respect to brightness, but also suggest that there is a parvocellular contribution to subjective contour sharpness.     

The age deficit on photopic counterphase flicker: contrast, spatial frequency, and luminance effects.

This study evaluated the contribution of reduced contrast sensitivity and retinal illuminance to the age-related deficit on the temporal resolution of suprathreshold spatial stimuli. The discrimination of counterphase flicker was measured in optimally refracted young and elderly observers for sinusoidal gratings of three spatial frequencies (1, 4, and 8 cycles per degree) at three contrast levels (0.11, 0.33, and 0.66). Age deficits in flicker discrimination at the two higher contrast levels and at the two lower spatial frequencies were unrelated to observer contrast sensitivity. Flicker discrimination of young observers who carried out the task through .5 ND filters to simulate a two-thirds reduction of retinal illuminance in the older eye, was similar to that of the elderly observers. An age-related reduction in retinal luminance appears to be a major determinant of the age-related spatiotemporal deficit at suprathreshold contrast levels, although neural factors may also be involved.     

Brightness enhancement and the Talbot level in stationary gratings

At low spatial frequencies, the perceived brightness of the light phase of a stationary square-wave grating is greater than the brightness of a solid field of equal physical luminance. That increase in the perceived brightness of a grating at low spatial frequencies is analogous to the brightness enhancement observed in a flickering light at low temporal frequencies. At or above the critical spatial frequency—the visual resolution threshold—the brightness of a grating is determined by its space-average luminance, just as the brightness of a flickering light at or above the critical flicker frequency is determined by its time-average luminance in accordance with Talbot’s law. Thus, Talbot’s law applies in the spatial as well as the temporal domain. The present study adds to the evidence that temporal and spatial frequency play analogous roles in some aspects of brightness vision.     

Voluntary attention increases perceived spatial frequency

Voluntary covert attention selects relevant sensory information for prioritized processing. The behavioral and neural consequences of such selection have been extensively documented, but its phenomenology has received little empirical investigation. Involuntary attention increases perceived spatial frequency (Gobell & Carrasco, 2005), but involuntary attention can differ from voluntary attention in its effects on performance in tasks mediated by spatial resolution (Yeshurun, Montagna, & Carrasco, 2008). Therefore, we ask whether voluntary attention affects the subjective appearance of spatial frequency—a fundamental dimension of visual perception underlying spatial resolution. We used a demanding rapid serial visual presentation task to direct voluntary attention and measured perceived spatial frequency at the attended and unattended locations. Attention increased the perceived spatial frequency of suprathreshold stimuli and also improved performance on a concurrent orientation discrimination task. In the control experiment, we ruled out response bias as an alternative account by using a lengthened interstimulus interval, which allows observers to disengage attention from the cued location. In contrast to the main experiment, the observers showed neither increased perceived spatial frequency nor improved orientation discrimination at the attended location. Thus, this study establishes that voluntary attention increases perceived spatial frequency. This phenomenological consequence links behavioral and neurophysiological studies on the effects of attention.     

Temporal ventriloquism in a purely temporal context

This study examines how audiovisual signals are combined in time for a temporal analogue of the ventriloquist effect in a purely temporal context, that is, no spatial grounding of signals or other spatial facilitation. Observers were presented with two successive intervals, each defined by a 1250-ms tone, and indicated in which interval a brief audiovisual stimulus (visual flash + noise burst) occurred later. In "test" intervals, the audiovisual stimulus was presented with a small asynchrony, while in "probe" intervals it was synchronous and presented at various times guided by an adaptive staircase to find the perceived temporal location of the asynchronous stimulus. As in spatial ventriloquism, and consistent with maximum likelihood estimation (MLE), the asynchronous audiovisual signal was shifted toward the more reliably localized component (audition, for all observers). Moreover, these temporal shifts could be forward or backward in time, depending on the asynchrony order, suggesting perceived timing is not entirely determined by physical timing. However, the critical signature of MLE combination--better bimodal than unimodal precision--was not found. Regardless of the underlying model, these results demonstrate temporal ventriloquism in a paradigm that is defined in a purely temporal context.     

Individual differences in vulnerability to subjective time distortion1

Time duration is perceived to be longer when accompanied by dynamic sensory stimulation than when accompanied by static stimulation. This distortion of time perception is thought to be due to the acceleration of an internal pacemaker that has been assumed to be the main component of temporal judgments. In order to investigate whether the function of the internal pacemaker is modality dependent or independent, we examined the correlation of visual flicker and auditory flutter effects on a temporal production task. While seeing a 10‐Hz visual flicker or hearing a 10‐Hz auditory flutter, participants estimated a duration of 2500 ms as accurately as possible by pressing a button. The results showed a significant within‐individual correlation between the time distortion due to visual flicker and that due to auditory flutter. Additionally, we found that time distortion due to auditory flutter tended to be larger in female participants than in male participants. These results suggest that the mechanisms underlying subjective time dilation are similar between vision and audition within individuals, but that they vary across individuals.     

Monocular without stereopsis with and head movement

Random dots moving with various velocity gradients were presented to observers; the motion was yoked to head movement in one condition and to no head movement in another. In Experiment 1, 12 observers were shown motion gradients with sine, triangle, sawtooth, and square waveforms with amplitudes (equivalent disparities) of 12′ and 1° 53′. In Experiment 2, 48 observers were shown only the sinewave or square-wave gradient of 1° 53′ disparity either with or without head movement so that the observers’ expectation to see depth in one condition did not transfer to another. The main findings were: (1) with 12′ disparity, the head-movement condition produced perceived depth but almost no perceived motion, whereas the no-head-movement condition produced both perceived depth and perceived motion; (2) with 1° 53′ disparity, both conditions produced perceived depth and perceived motion; and (3) when the expectation to see depth was removed, the no-head-movement condition with the square-wave gradient produced no perceived depth, only motion. We suggest that monocular stereopsis with head movement can be achieved without perception of motion but monocular stereopsis without head movement requires perception of motion.     

Flicker-light induced visual phenomena: frequency dependence and specificity of whole percepts and percept features

Flickering light induces visual hallucinations in human observers. Despite a long history of the phenomenon, little is known about the dependence of flicker-induced subjective impressions on the flicker frequency. We investigate this question using Ganzfeld stimulation and an experimental paradigm combining a continuous frequency scan (1–50 Hz) with a focus on re-occurring, whole percepts. On the single-subject level, we find a high degree of frequency stability of percepts. To generalize across subjects, we apply two rating systems, (1) a set of complex percept classes derived from subjects’ reports and (2) an enumeration of elementary percept features, and determine distributions of occurrences over flicker frequency. We observe a stronger frequency specificity for complex percept classes than elementary percept features. Comparing the similarity relations among percept categories to those among frequency profiles, we observe that though percepts are preferentially induced by particular frequencies, the frequency does not unambiguously determine the experienced percept.