The roles of contour and luminance distribution in determining perceived centers within shapes

Two sources of visual information that likely could be employed by the perceptual system in locating the centers of bounded shapes—boundary configuration and luminance distribution—have been perfectly confounded in every study thus far aimed at investigating perceived centters. Observers, using either a revolving or stationary x-y plotter, made judgments on the location of centers within either revolving or stationary shapes of both uniform and varied luminance distributions. Results indicate that the location of perceived centers depended predominantly upon boundary contour and was affected by the distribution of luminance within these edges to a much lesser degree.     

Dynamic grouping and interpolation induced by flickering stimuli

A novel grouping and interpolation effect induced by flickering stimuli is described: a matrix of flickering elements forms stick-like clusters, then the clusters gradually dissociate back into the discrete elements within a few seconds. On continuous viewing, this flicker-induced grouping and interpolation repeatedly disappeared and reappeared. The perceived strength of this phenomenon peaked when the luminance of the flickering elements was alternately darker and lighter than the background; thus, the reversal of the luminance contrast polarity was responsible for flicker-induced grouping. The temporal dynamics of flicker-induced grouping showed the stochastic nature of perceptual alternation, which depended on the global structure of the stimulus. From these results, it is concluded that flicker-induced grouping reflects multiple stages of visual processing.     

Efficient visual search without top-down or bottom-up guidance

Two types of mechanisms have dominated theoretical accounts of efficient visual search. The first are bottom-up processes related to the characteristics of retinotopic feature maps. The second are top-down mechanisms related to feature selection. To expose the potential involvement of other mechanisms, we introduce a new search paradigm whereby a target is defined only in a context-dependent manner by multiple conjunctions of feature dimensions. Because targets in a multiconjunction task cannot be distinguished from distractors either by bottom-up guidance or top-down guidance, current theories of visual search predict inefficient search. While inefficient search does occur for the multiple conjunctions of orientation with color or luminance, we find efficient search for multiple conjunctions of luminance/size, luminance/shape, and luminance/topology. We also show that repeated presentations of either targets or a set of distractors result in much faster performance and that bottom-up feature extraction and top-down selection cannot account for efficient search on their own. In light of this, we discuss the possible role of perceptual organization in visual search. Furthermore, multiconjunction search could provide a new method for investigating perceptual grouping in visual search.     

Multistable phenomena: changing views in perception

Traditional explanations of multistable visual phenomena (e.g. ambiguous figures, perceptual rivalry) suggest that the basis for spontaneous reversals in perception lies in antagonistic connectivity within the visual system. In this review, we suggest an alternative, albeit speculative, explanation for visual multistability – that spontaneous alternations reflect responses to active, programmed events initiated by brain areas that integrate sensory and non-sensory information to coordinate a diversity of behaviors. Much evidence suggests that perceptual reversals are themselves more closely related to the expression of a behavior than to passive sensory responses: (1) they are initiated spontaneously, often voluntarily, and are influenced by subjective variables such as attention and mood; (2) the alternation process is greatly facilitated with practice and compromised by lesions in non-visual cortical areas; (3) the alternation process has temporal dynamics similar to those of spontaneously initiated behaviors; (4) functional imaging reveals that brain areas associated with a variety of cognitive behaviors are specifically activated when vision becomes unstable. In this scheme, reorganizations of activity throughout the visual cortex, concurrent with perceptual reversals, are initiated by higher, largely non-sensory brain centers. Such direct intervention in the processing of the sensory input by brain structures associated with planning and motor programming might serve an important role in perceptual organization, particularly in aspects related to selective attention.     

Visual training improves perceptual grouping based on basic stimulus features

Training on visual tasks improves performance on basic and higher order visual capacities. Such improvement has been linked to changes in connectivity among mediating neurons. We investigated whether training effects occur for perceptual grouping. It was hypothesized that repeated engagement of integration mechanisms would enhance grouping processes. Thirty-six participants underwent 15 sessions of training on a visual discrimination task that required perceptual grouping. Participants viewed 20?×?20 arrays of dots or Gabor patches and indicated whether the array appeared grouped as vertical or horizontal lines. Across trials stimuli became progressively disorganized, contingent upon successful discrimination. Four visual dimensions were examined, in which grouping was based on similarity in luminance, color, orientation, and motion. Psychophysical thresholds of grouping were assessed before and after training. Results indicate that performance in all four dimensions improved with training. Training on a control condition, which paralleled the discrimination task but without a grouping component, produced no improvement. In addition, training on only the luminance and orientation dimensions improved performance for those conditions as well as for grouping by color, on which training had not occurred. However, improvement from partial training did not generalize to motion. Results demonstrate that a training protocol emphasizing stimulus integration enhanced perceptual grouping. Results suggest that neural mechanisms mediating grouping by common luminance and/or orientation contribute to those mediating grouping by color but do not share resources for grouping by common motion. Results are consistent with theories of perceptual learning emphasizing plasticity in early visual processing regions.     

Perceptual, oculomotor, and neural responses to moving color plaids

Moving plaids constructed from two achromatic gratings of identical luminance contrast are known to yield a percept of coherent pattern motion, as are plaids constructed from two identical chromatic (e.g. isoluminant red/green) gratings. To examine the interactive influences of chromatic and luminance contrast on the integration of visual motion signals, we constructed plaids with gratings that possessed both forms of contrast. We used plaids of two basic types, which differed with respect to the phase relationship between chromatic and luminance modulations (after Kooi et al, 1992 Perception 21 583-598). One plaid type ('symmetric') was made from component gratings that had identical chromatic/luminance phase relationships (e.g. both components were red-bright/green-dark modulation). The second plaid type ('asymmetric') was made from components that had complimentary phase relationships (i.e. one red-bright/green-dark grating and one green-bright/red-dark grating). Human subjects reported that the motion of symmetric plaids was perceptually coherent, while the components of asymmetric plaids failed to cohere. We also recorded eye movements elicited by both types of plaids to determine if they are similarly affected by these image cues for motion coherence. Results demonstrate that, under many conditions, eye movements elicited by perceptually coherent vs noncoherent plaids are distinguishable from one another. To reveal the neural bases of these perceptual and oculomotor phenomena, we also recorded the responses of neurons in the middle temporal visual area (area MT) of macaque visual cortex. Here we found that individual neurons exhibited differential tuning to symmetric vs asymmetric plaids. These neurophysiological results demonstrate that the neural mechanism for motion coherence is sensitive to the phase relationship between chromatic and luminance contrast, a finding which has implications for interactions between 'color' and 'motion' processing streams in the primate visual system.     

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.     

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.     

Visual binding of English and Chinese word parts is limited to low temporal frequencies

Some perceptual mechanisms manifest high temporal precision, allowing reports of visual information even when that information is restricted to windows smaller than 50 ms. Other visual judgments are limited to much coarser time scales. What about visual information extracted at late processing stages, for which we nonetheless have perceptual expertise, such as words? Here, the temporal limits on binding together visual word parts were investigated. In one trial, either the word 'ball' was alternated with 'deck', or 'dell' was alternated with 'back', with all stimuli presented at fixation. These stimuli restrict the time scale of the rod identities because the two sets of alternating words form the same image at high alternation frequencies. Observers made a forced choice between the two alternatives. Resulting 75% thresholds are restricted to 5 Hz or less for words and nonword letter strings. A similar result was obtained in an analogous experiment with Chinese participants viewing alternating Chinese characters. These results support the theory that explicit perceptual access to visual information extracted at late stages is limited to coarse time scales.     

Effects of absolute luminance and luminance contrast on visual discrimination in low mesopic environments

Recent research revealed considerable decline in visual perception under low luminance conditions. However, systematic studies on how visual performance is affected by absolute luminance and luminance contrast under low mesopic conditions (<0.5 cd/m²) is lacking. We examined performance in a simple visual discrimination task under low mesopic luminance conditions in three experiments in which we systematically varied base luminance and luminance contrast between stimulus and background. We further manipulated eccentricity of the stimuli because of known rods and cones gradients along the retina. We identified a “deficiency window” for performance as measured by d’ when luminance was < 0.06 cd/m² and luminance contrast as measured by the luminance ratio between stimulus and background was below < 1.7. We further calculated performance-based luminance as well as contrast efficiency functions for reaction times (RTs). These power functions demonstrate the contrast asymptote needed to decrease RTs and how such a decrease can be achieved given various combinations of absolute luminance and luminance contrast manipulations. Increased eccentricity resulted in slower RTs indicative of longer scan distances. Our data provide initial insights to performance-based efficiency functions in low mesopic environments that are currently lacking and to the physical mechanisms being utilized for visual perception in these extreme environments.     

Symbolic magnitude modulates perceptual strength in binocular rivalry

Basic aspects of magnitude (such as luminance contrast) are directly represented by sensory representations in early visual areas. However, it is unclear how symbolic magnitudes (such as Arabic numerals) are represented in the brain. Here we show that symbolic magnitude affects binocular rivalry: perceptual dominance of numbers and objects of known size increases with their magnitude. Importantly, variations in symbolic magnitude acted like variations in luminance contrast: we found that an increase in numerical magnitude of adding one lead to an equivalent increase in perceptual dominance as a contrast increment of 0.32%. Our results support the claim that magnitude is extracted automatically, since the increase in perceptual dominance came about in the absence of a magnitude-related task. Our findings show that symbolic, acculturated knowledge about magnitude interacts with visual perception and affects perception in a manner similar to lower-level aspects of magnitude such as luminance contrast.     

The hare and the snail: Dissociating visual orienting from conscious perception

A method for investigating attentional effects of peripheral visual objects, independently of perceptual identification, is described. We report an experiment using this method which shows that visual processing of peripheral objects differs radically, depending on whether participants move attention in response to an object or consciously perceive that object. When luminance contrast was reduced, conscious perceptual discrimination of peripheral letters was massively slower and less accurate—but both low and high contrast letters elicited rapid attentional orienting effects and these rapid orienting effects were equal in magnitude across low and high contrast. This pattern is consistent with known differences in luminance sensitivity between the dorsal and ventral visual processing streams, and with rapid dorsal–ventral interaction mediated via re-entrant feedback. Our findings show that the control system responsible for rapid movements of attention is exquisitely sensitive to visual form information at low levels of contrast, and involves a different neurocognitive pathway to that which gives rise to conscious perception.     

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.     

Non-transient luminance changes do not capture attention

The processing of luminance change is a ubiquitous feature of the human visual system and provides the basis for the rapid orienting of attention to potentially important events (e.g., motion onset, object onset). However, despite its importance for attentional capture, it is not known whether a luminance change attracts attention solely because of its status as a sensory transient or can attract attention at a relatively high cognitive level. In a series of six experiments, we presented visual displays in which a single object underwent a luminance change that was either visible or obscured by a mask. A target then appeared either at the change location or elsewhere. The results showed that the luminance change attracted attention only in the visible condition. This was even observed with the largest change we could generate (> 75 cd/m(2)). These data suggest that the importance of a luminance change is only in its status as a low-level sensory transient.     

Visual search in a multi-element asynchronous dynamic (MAD) world

In visual search tasks participants search for a target among distractors in strictly controlled displays. We show that visual search principles observed in these tasks do not necessarily apply in more ecologically valid search conditions, using dynamic and complex displays. A multi-element asynchronous dynamic (MAD) visual search was developed in which the stimuli could either be moving, stationary, and/or changing in luminance. The set sizes were high and participants did not know the specific target template. Experiments 1 through 4 showed that, contrary to previous studies, search for moving items was less efficient than search for static items and targets were missed a high percentage of the time. However, error rates were reduced when participants knew the exact target template (Experiment 5) and the difference in search efficiency for moving and stationary targets disappeared when lower set sizes were used (Experiment 6). In all experiments there was no benefit to finding targets defined by a luminance change. The data show that visual search principles previously shown in the literature do not apply to these more complex and "realistically" driven displays.     

The effect of generation on long-term repetition priming in auditory and visual perceptual identification

Perceptual implicit memory is typically most robust when the perceptual processing at encoding matches the perceptual processing required during retrieval. A consistent exception is the robust priming that semantic generation produces on the perceptual identification test (Masson & MacLeod, 2002), a finding which has been attributed to either (1) conceptual influences in this nominally perceptual task, or (2) covert orthographic processing during generative encoding. The present experiments assess these possibilities using both auditory and visual perceptual identification, tests in which participants identify auditory words in noise or rapidly-presented visual words. During the encoding phase of the experiments, participants generated some words and perceived others in an intermixed study list. The perceptual control condition was visual (reading) or auditory (hearing), and varied across participants. The reading and hearing conditions exhibited the expected modality–specificity, producing robust intra-modal priming and non-significant cross-modal priming. Priming in the generate condition depended on the perceptual control condition. With a read control condition, semantic generation produced robust visual priming but no auditory priming. With a hear control condition, the results were reversed: semantic generation produced robust auditory priming but not visual priming. This set of results is not consistent with a straightforward application of either the conceptual-influence or covert-orthography account, and implies that the nature of encoding in the generate condition is influenced by the broader list context.     

Visual motion and attentional capture

Previous work has shown that abrupt visual onsets capture attention. This occurs even with stimuli that are equiluminant with the background, which suggests that the appearance of a new perceptual object, not merely a change in luminance, captures attention. Three experiments are reported in which this work was extended by investigating the possible role of visual motion in attentional capture. Experiment 1 revealed that motion can efficiently guide attention when it is perfectly informative about the location of a visual search target, but that it does not draw attention when it does not predict the target’s position. This result was obtained with several forms of motion, including oscillation, looming, and nearby moving contours. To account for these and other results, we tested anew-object account of attentional capture in Experiment 2 by using a global/local paradigm. When motion segregated a local letter from its perceptual group, the local letter captured attention as indexed by an effect on latency of response to the task-relevant global configuration. Experiment 3 ruled out the possibility that the motion in Experiment 2 captured attention merely by increasing the salience of the moving object. We argue instead that when motion segregates a perceptual element from a perceptual group, a new perceptual object is created, and this event captures attention. Together, the results suggest that motion as such does not capture attention but that the appearance of a new perceptual object does.     

Judgments of synchrony between auditory and moving or still visual stimuli.

The flash-lag effect is a visual illusion wherein intermittently flashed, stationary stimuli seem to trail after a moving visual stimulus despite being flashed synchronously. We tested hypotheses that the flash-lag effect is due to spatial extrapolation, shortened perceptual lags, or accelerated acquisition of moving stimuli, all of which call for an earlier awareness of moving visual stimuli over stationary ones. Participants judged synchrony of a click either to a stationary flash of light or to a series of adjacent flashes that seemingly bounced off or bumped into the edge of the visual display. To be judged synchronous with a stationary flash, audio clicks had to be presented earlier--not later--than clicks that went with events, like a simulated bounce (Experiment 1) or crash (Experiments 2-4), of a moving visual target. Click synchrony to the initial appearance of a moving stimulus was no different than to a flash, but clicks had to be delayed by 30-40 ms to seem synchronous with the final (crash) positions (Experiment 2). The temporal difference was constant over a wide range of motion velocity (Experiment 3). Interrupting the apparent motion by omitting two illumination positions before the last one did not alter subjective synchrony, nor did their occlusion, so the shift in subjective synchrony seems not to be due to brightness contrast (Experiment 4). Click synchrony to the offset of a long duration stationary illumination was also delayed relative to its onset (Experiment 5). Visual stimuli in motion enter awareness no sooner than do stationary flashes, so motion extrapolation, latency difference, and motion acceleration cannot explain the flash-lag effect.     

Visual perception and aging.

A series of studies performed in our laboratory on aging and its effect on perceptual processing and working memory capacity for visual stimuli are reviewed. Specifically, studies on luminance, colour, motion, texture, and symmetry processing are reported. Furthermore, experiments on the capacity to retain size and spatial frequency information are also discussed. The general conclusion is that there are a number of perceptual abilities that diminish with age. However, the extent of these deficits will depend on the complexity of the neural circuitry involved for processing a given task. This is also true for visual working memory where no evidence of loss due to aging is demonstrated for processing low-level visual information, when individual differences in sensory input are compensated for. It is concluded that perceptual processing deficits due to aging (like working memory) will become evident when the computational load reaches a certain level of complexity (larger or more complex network) even if the tasks remain cognitively simple.     

Transparency: relation to depth, subjective contours, luminance, and neon color spreading

The perception of transparency is highly dependent on luminance and perceived depth. An image region is seen as transparent if it is of intermediate luminance relative to adjacent image regions, and if it is perceived in front of another region and has a boundary which provides information that an object is visible through this region. Yet, transparency is not just the passive end-product of these required conditions. If perceived transparency is triggered, a number of seemingly more elemental perceptual primitives such as color, contour, and depth can be radically altered. Thus, with the perception of transparency, neon color spreading becomes apparent, depth changes, stereoscopic depth capture can be eliminated, and otherwise robust subjective contours can be abolished. In addition, we show that transparency is not coupled strongly to real-world chromatic constraints since combinations of luminance and color which would be unlikely to arise in real-world scenes still give rise to the perception of transparency. Rather than seeing transparency as a perceptual end-point, determined by seemingly more primitive processes, we interpret perceived transparency as much a 'cause', as an 'effect'. We speculate that the anatomical substrate for such mutual interaction may lie in cortical feed-forward connections which maintain modular segregation and cortical feedback connections which do not.