The role of mask coherence in motion-induced blindness

Motion-induced blindness (MIB) is the perceived disappearance of a salient target when surrounded by a moving mask. Much research has focused on the role of target characteristics on perceived disappearance by a coherently moving mask. However, we asked a different question: mainly, are there certain characteristics about the mask that can impact disappearance? To address this, we behaviorally tested whether MIB is enhanced or reduced by the property of common fate. In experiments 1, 2, and 3, we systematically manipulated the motion coherence of the mask and measured the amount of target disappearance. Results showed that, as mask coherence increased, perceived target disappearance decreased. This pattern was unaffected by the lifetime of the moving dots, the dot density of the motion stimulus, or the target eccentricity. In experiment 4, we investigated whether the number of motion directions contained in an incoherent mask could account for our findings. Using masks containing 1, 3, and 5 motion directions, we found that disappearance did not increase proportionally to the number of motion directions. We discuss our findings in line with current proposed mechanisms of MIB.     

Does interhemispheric competition mediate motion-induced blindness? A transcranial magnetic stimulation study

Motion-induced blindness (MIB) is a phenomenon, perhaps related to perceptual rivalry, where stationary targets disappear and reappear in a cyclic mode when viewed against a background (mask) of coherent, apparent 3-D motion. Since MIB has recently been shown to share similar temporal properties with binocular rivalry, we probed the appearance-disappearance cycle of MIB using unilateral, single-pulse transcranial magnetic stimulation (TMS)--a manipulation that has previously been shown to influence binocular rivalry. Effects were seen for both hemispheres when the timing of TMS was determined prospectively on the basis of a given subject's appearance-disappearance cycle, so that it occurred on average around 300 ms before the time of perceptual switch. Magnetic stimulation of either hemisphere shortened the time to switch from appearance to disappearance and vice versa. However, TMS of left posterior parietal cortex more selectively shortened the disappearance time of the targets if delivered in phase with the disappearance cycle, but lengthened it if TMS was delivered in the appearance phase after the perceptual switch. Opposite effects were seen in the right hemisphere, although less marked than the left-hemisphere effects. As well as sharing temporal characteristics with binocular rivalry, MIB therefore seems to share a similar underlying mechanism of interhemispheric modulation. Interhemispheric switching may thus provide a common temporal framework for uniting the diverse, multilevel phenomena of perceptual rivalry.     

Delayed offset of distracters masks a local target

Object substitution masking (OSM) is observed when a brief target surrounded with a mask is presented among distracter stimuli and cannot be identified when it and the distracters disappear but the mask remains in view. We probed whether OSM also occurs without a local mask object when the distracters remain after target offset. We also varied the congruence between the local target and the global search display and the grouping properties of the delayed offset distracters. A target was briefly presented in a global object configuration of distracters that had delayed offset. Results showed that OSM could be observed with delayed offset of distracters grouped into a global mask shape. Congruence of the shapes of the global and local objects did not affect OSM, suggesting that a generalized abstract visual pattern representation of the global object may not be involved in OSM nor did the grouping properties of the delayed offset distracters influence OSM.     

Object substitution masking and the object updating hypothesis

The object updating hypothesis of object substitution masking proposes that the phenomenon arises when the visual system fails to individuate target and mask at the level of object token representations. This hypothesis is tested in two experiments using modifications of the dot mask paradigm developed by Lleras and Moore (2003). Target—mask individuation is manipulated by the presentation of additional display items that influence the linking apparent motion seen between a target and a spatially separated mask (Experiment 1), and by the use of placeholders that maintain the target object’s presence during mask presentation (Experiment 2). Results in both cases are consistent with the updating hypothesis in showing significantly reduced masking when the conditions promoted target—mask individuation. However, in both experiments, some masking was still present under conditions of individuation, an effect we attribute to attentional capture by the mask.     

Object substitution masking: when does mask preview work?

When a target is enclosed by a 4-dot mask that persists after the target disappears, target identification is worse than it is when the mask terminates with the target. This masking effect is attributed to object substitution masking (OSM). Previewing the mask, however, attenuates OSM. This study investigated specific conditions under which mask preview was, or was not, effective in attenuating masking. In Experiment 1, the interstimulus interval (ISI) between previewed mask offset and target presentation was manipulated. The basic preview effect was replicated; neither ISI nor preview duration influenced target identification performance. In Experiment 2, mask configurations were manipulated. When the mask configuration at preview matched that at target presentation, the preview effect was replicated. New evidence of ineffective mask preview was found: When the two configurations did not match, performance declined. Yet, when the ISI between previewed mask offset and target presentation was removed such that the mask underwent apparent motion, preview was effective despite the configuration mismatch. An interpretation based on object representations provides an excellent account of these data.     

Visual search asymmetries in motion and optic flow fields

In visual search, items defined by a unique feature are found easily and efficiently. Search for a moving target among stationary distractors is one such efficient search. Search for a stationary target among moving distractors is markedly more difficult. In the experiments reported here, we confirm this finding and further show that searches for a stationary target within a structured flow field are more efficient than searches for stationary targets among distractors moving in random directions. The structured motion fields tested included uniform direction of motion, a radial flow field simulating observer forward motion, and a deformation flow field inconsistent with observer motion. The results using optic flow stimuli were not significantly different from the results obtained with other structured fields of distractors. The results suggest that the local properties of the flow fields rather than global optic flow properties are important for determining the efficiency of search for a stationary target.     

Visual search asymmetries in motion and optic flow fields.

In visual search, items defined by a unique feature are found easily and efficiently. Search for a moving target among stationary distractors is one such efficient search. Search for a stationary target among moving distractors is markedly more difficult. In the experiments reported here, we confirm this finding and further show that searches for a stationary target within a structured flow field are more efficient than searches for stationary targets among distractors moving in random directions. The structured motion fields tested included uniform direction of motion, a radial flow field simulating observer forward motion, and a deformation flow field inconsistent with observer motion. The results using optic flow stimuli were not significantly different from the results obtained with other structured fields of distractors. The results suggest that the local properties of the flow fields rather than global optic flow properties are important for determining the efficiency of search for a stationary target.     

Visual guidance of intercepting a moving target on foot

How do people walk to a moving target, and what visual information do they use to do so? Under a pursuit strategy, one would head toward the target's current position, whereas under an interception strategy, one would lead the target, ideally by maintaining a constant target-heading angle (or constant bearing angle). Either strategy may be guided by the egocentric direction of the target, local optic flow from the target, or global optic flow from the background. In four experiments, participants walked through a virtual environment to reach a target moving at a constant velocity. Regardless of the initial conditions, they walked ahead of the target for most of a trial at a fairly constant speed, consistent with an interception strategy (experiment 1). This behavior can be explained by trying to maintain a constant target-heading angle while trying to walk a straight path, with transient steering dynamics. In contrast to previous results for stationary targets, manipulation of the local optic flow from the target (experiment 2) and the global optic flow of the background (experiments 3 and 4) failed to influence interception behavior. Relative motion between the target and the background did affect the path slightly, presumably owing to its effect on perceived target motion. We conclude that humans use an interception strategy based on the egocentric direction of a moving target.     

When the target becomes the mask: using apparent motion to isolate the object-level component of object substitution masking

J. T. Enns and V. Di Lollo (1997) discovered a new form of visual masking that they labeled object substitution masking (OSM). OSM occurs when 4 dots, presented around a target, trail in the display after target offset. The present study showed that the physical presence of the masking dots after target offset is not necessary for OSM. Instead, the continued presence of a changing high-level representation associated with the target suffices to yield OSM. Apparent motion was used to define such representation. In these experiments, the initial display offset and was followed by a 2nd display where masks appeared at new locations. Only when the spatiotemporal properties of the stimuli on the 2nd display supported the perception of the target moving and turning into the mask was OSM observed.     

The effect of body and part-based motion on the recognition of unfamiliar objects

We investigated the role of global (body) and local (parts) motion on the recognition of unfamiliar objects. Participants were trained to categorise moving objects and were then tested on their recognition of static images of these targets using a priming paradigm. Each static target shape was primed by a moving object that comprised either the same body and parts motion; same body, different parts motion; different body, same part motion as the learned target or was non-moving. Only the same body but not the same part motion facilitated shape recognition (Experiment 1), even when either motion was diagnostic of object identity (Experiment 2). When parts motion was more related to the object's body motion then it facilitated the recognition of the static target (Experiment 3). Our results suggest that global and local motions are independently accessed during object recognition and have important implications for how objects are represented in memory.     

Grouping and trajectory storage in multiple object tracking: impairments due to common item motions

In our natural viewing, we notice that objects change their locations across space and time. However, there has been relatively little consideration of the role of motion information in the construction and maintenance of object representations. We investigated this question in the context of the multiple object tracking (MOT) paradigm, wherein observers must keep track of target objects as they move randomly amid featurally identical distractors. In three experiments, we observed impairments in tracking ability when the motions of the target and distractor items shared particular properties. Specifically, we observed impairments when the target and distractor items were in a chasing relationship or moved in a uniform direction. Surprisingly, tracking ability was impaired by these manipulations even when observers failed to notice them. Our results suggest that differentiable trajectory information is an important factor in successful performance of MOT tasks. More generally, these results suggest that various types of common motion can serve as cues to form more global object representations even in the absence of other grouping cues.     

The effect of spatial competition between object-level representations of target and mask on object substitution masking

One of the processes determining object substitution masking (OSM) is thought to be the spatial competition between independent object file representations of the target and mask (e.g., Kahan & Lichtman, 2006). In a series of experiments, we further examined how OSM is influenced by this spatial competition by manipulating the overlap between the surfaces created by the modal completion of the target (an outline square with a gap in one of its sides) and the mask (a four-dot mask). The results of these experiments demonstrate that increasing the spatial overlap between the surfaces of the target and mask increases OSM. Importantly, this effect is not caused by the mask interfering with the processing of the target features it overlaps. Overall, the data indicate, consistent with Kahan and Lichtman, that OSM can arise through competition between independent target and mask representations.     

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.     

How an abrupt onset cue can release motion-induced blindness

In motion-induced blindness (MIB), a target within rotating random dots is occasionally hidden from observers' consciousness during observation. In the present study, a red ring-like cue was centered on a target and presented immediately after observers reported subjective disappearance of the target in MIB (Experiment 1). The radius of the cue was systematically modulated. Observers quickly regained awareness of the disappeared object only after they were provided with a pinpoint cue of its location. We also found that a flickering cue at 1Hz hindered MIB when the radius of the cue was critically small (Experiment 2). Furthermore, abrupt onset of a small square was enough to regain awareness of the target (Experiment 3). Successful revival of the target with a small cue indicates that critical spatial distribution of visual attention determines what in the visual scene is included in visual awareness.     

Motion-induced blindness measured objectively

During central fixation, a moving pattern of nontargets induces repeated temporary blindness to even salient peripheral targets: motion-induced blindness (MIB). Hitherto, behavioral measures of MIB have relied on subjective judgments. Here, we offer an objective alternative that builds on earlier findings regarding the effects of MIB on the detectability of physical target offsets. We propose a small modification of regular MIB displays: Following a variable duration (lead time), one of the targets is physically removed. Subjects are to respond immediately afterward. We hypothesize that illusory target offsets, caused by MIB, are mistaken for physical target offsets and that errors should thus increase with lead time. Indeed, for both nonsalient and salient targets, we found that detection accuracy for physical target offsets dramatically decreased with lead time. We conclude that target offset detection accuracy is a valid objective measure of MIB. With our method, effects of guessing are minimal, and the fitting of psychometric functions is straightforward. In principle, a staircase extension—for more efficient data collection—is also possible.     

The effect of experience and of dots’ density and duration on the detection of coherent motion in dogs

Knowledge about the mechanisms underlying canine vision is far from being exhaustive, especially that concerning post-retinal elaboration. One aspect that has received little attention is motion perception, and in spite of the common belief that dogs are extremely apt at detecting moving stimuli, there is no scientific support for such an assumption. In fact, we recently showed that dogs have higher thresholds than humans for coherent motion detection (Kanizsar et al. in Sci Rep UK 7:11259, 2017). This term refers to the ability of the visual system to perceive several units moving in the same direction, as one coherently moving global unit. Coherent motion perception is commonly investigated using random dot displays, containing variable proportions of coherently moving dots. Here, we investigated the relative contribution of local and global integration mechanisms for coherent motion perception, and changes in detection thresholds as a result of repeated exposure to the experimental stimuli. Dogs who had been involved in the previous study were given a conditioned discrimination task, in which we systematically manipulated dot density and duration and, eventually, re-assessed our subjects’ threshold after extensive exposure to the stimuli. Decreasing dot duration impacted on dogs’ accuracy in detecting coherent motion only at very low duration values, revealing the efficacy of local integration mechanisms. Density impacted on dogs’ accuracy in a linear fashion, indicating less efficient global integration. There was limited evidence of improvement in the re-assessment but, with an average threshold at re-assessment of 29%, dogs’ ability to detect coherent motion remains much poorer than that of humans.     

Orientation-selective adaptation during motion-induced blindness

When a global moving pattern is superimposed on high-contrast stationary or slowly moving stimuli, the latter occasionally disappear for periods of several seconds (motion-induced blindness, MIB). Here, an adaptation paradigm was used to determine if orientation-selective adaptation still occurs for the stimulus that is no longer visible. Two slowly drifting high-contrast Gabor patches were presented to observers. As soon as both patches disappeared, one was eliminated from the screen. After 2 s, two low-contrast Gabor patches were presented as tests at the same locations and observers were asked to report their orientations. The observers' performance was significantly higher when the orientation of the low-contrast test patch was orthogonal to the orientation of the high-contrast adapting patch (p < 0.0001) for the location where the patch was present during MIB, even though it was perceptually invisible. The observers' performance was not significantly different at the adjacent control location where the stimulus was absent during the MIB. Although no stimulus was visible at either location, orientation-selective adaptation was preserved only for the location at which the patch remained present. Since orientation information is processed in low-level visual areas such as the primary visual cortex (V1), we conclude that MIB originates in an area higher than V1.     

Induced motion: isolation and dissociation of egocentric and vection-entrained components.

Induced motion (IM) is illusory motion of a stationary test target opposite to the direction of the real motion of the inducing stimulus. We define egocentric IM as an apparent motion of the test target relative to the observer, and vection-entrained IM as an apparent motion of a stationary object along with an apparent motion of the self (vection) induced by the same stimulus. These two forms of IM are often confounded, and tests for distinguishing between them have not been devised. We have devised such tests. Our test for egocentric IM relies on evidence that this form of IM is due mainly to a misregistration of eye movements when optokinetic nystagmus (OKN) is inhibited, and on evidence that OKN is evoked only by stimuli in the plane of convergence. Our test for vection-entrained IM relies on evidence that vection is evoked only by the more distant of two superimposed inducing stimuli. Thus we found egocentric IM to be induced without vection or vection-entrained IM when subjects converged on a foreground moving display with a stationary display in the background, and vection-entrained IM to be induced without egocentric IM when subjects converged on a stationary-foreground display with a moving display in the background. The two types of IM were evoked in opposite directions at the same time when subjects converged on a foreground moving display while a background display moved in the opposite direction. The two forms of IM showed no signs of interaction, and we conclude that they rely on independent motion mechanisms that operate within distinct frames of reference. A control experiment suggested that the depth adjacency effect in IM is determined by the depth adjacency of the inducing stimulus to convergence, not just to the test target.     

The surface and deep structure of the waterfall illusion

The surface structure of the waterfall illusion or motion aftereffect (MAE) is its phenomenal visibility. Its deep structure will be examined in the context of a model of space and motion perception. The MAE can be observed following protracted observation of a pattern that is translating, rotating, or expanding/contracting, a static pattern appears to move in the opposite direction. The phenomenon has long been known, and it continues to present novel properties. One of the novel features of MAEs is that they can provide an ideal visual assay for distinguishing local from global processes. Motion during adaptation can be induced in a static central grating by moving surround gratings; the MAE is observed in the static central grating but not in static surrounds. The adaptation phase is local and the test phase is global. That is, localised adaptation can be expressed in different ways depending on the structure of the test display. These aspects of MAEs can be exploited to determine a variety of local/global interactions. Six experiments on MAEs are reported. The results indicated that relational motion is required to induce an MAE; the region adapted extends beyond that stimulated; storage can be complete when the MAE is not seen during the storage period; interocular transfer (IOT) is around 30% of monocular MAEs with phase alternation; large field spiral patterns yield MAEs with characteristic monocular and binocular interactions.     

Reading action word affects the visual perception of biological motion

In the present study, we investigate whether reading an action-word can influence subsequent visual perception of biological motion. The participant's task was to perceptually judge whether a human action identifiable in the biological motion of a point-light display embedded in a high density mask was present or not in the visual sequence, which lasted for 633 ms on average. Prior to the judgement task, participants were exposed to an abstract verb or an action verb for 500 ms, which was related to the human action according to a congruent or incongruent semantic relation. Data analysis showed that correct judgements were not affected by action verbs, whereas a facilitation effect on response time (49 ms on average) was observed when a congruent action verb primed the judgement of biological movements. In relation with the existing literature, this finding suggests that the perception, the planning and the linguistic coding of motor action are subtended by common motor representations.