Learning influences the encoding of static and dynamic faces and their recognition across different spatial frequencies

Studies on face recognition have shown that observers are faster and more accurate at recognizing faces learned from dynamic sequences than those learned from static snapshots. Here, we investigated whether different learning procedures mediate the advantage for dynamic faces across different spatial frequencies. Observers learned two faces—one dynamic and one static—either in depth (Experiment 1) or using a more superficial learning procedure (Experiment 2). They had to search for the target faces in a subsequent visual search task. We used high-spatial frequency (HSF) and low-spatial frequency (LSF) filtered static faces during visual search to investigate whether the behavioural difference is based on encoding of different visual information for dynamically and statically learned faces. Such encoding differences may mediate the recognition of target faces in different spatial frequencies, as HSF may mediate featural face processing whereas LSF mediates configural processing. Our results show that the nature of the learning procedure alters how observers encode dynamic and static faces, and how they recognize those learned faces across different spatial frequencies. That is, these results point to a flexible usage of spatial frequencies tuned to the recognition task.     

The relationship between apparent motion and object files

Object files (OFs) play an important role in theories of mid-level vision. On some influential views, OFs operate and persist only via spatiotemporal continuity. One open question concerns what occurs when direct spatiotemporal continuity is absent: Do OFs move in accordance with any motion correspondence ultimately resolved? Specifically, do OFs accord with apparent motion (AM) correspondences, which arise despite a lack of continuous spatiotemporal stimulation? In Experiment 1, subjects were presented with an AM display consisting of two circles that, across two frames, were seen as moving between two noncontiguous locations. The two objects were primed with two symbols and were then moved in a single step; a third symbol appeared, and could either match the symbol from the closer or the further object. We found a robust object specific preview benefit (OSPB) for the shorter path, in other words, the path along which AM was perceived. In order to control for the possibility that priming occurs at any nearby object, in Experiment 2, the original two objects never disappeared, but two new objects appeared in the would-be AM locations. No AM was perceived, and no OSPB obtained. In the third experiment the OSPB effect persisted even when motion along the shorter path included an unlikely featural transformation (circles turning into squares). In Experiment 4, which was nearly identical to Experiment 2, no OSPB obtained despite unique featural matches between the initial and new objects, seemingly because no AM was perceived. In Experiment 5, we failed to find an effect of featural priming, even when distance between the objects was equated. Finally, we extended the OSPB effect to two additional kinds of AM—line motion (Experiment 6) and phi motion (Experiment 7), supplying strong evidence that AM correspondences and OF correspondences are controlled by the same basic rules.     

Learned prediction affects body perception

Learning to recognize objects appears to depend critically on extended observation of appearance over time. Specifically, temporal association between dissimilar views of an object has been proposed as a tool for learning invariant representations for recognition. We examined heretofore untested aspects of the temporal association hypothesis using a familiar dynamic object, the human body. Specifically, we examined the role of appearance prediction (temporal asymmetry) in temporal association. In our task, observers performed a change detection task using upright and inverted images of a walking body either with or without previous exposure to a motion stimulus depicting an upright walker. Observers who were exposed to the dynamic stimulus were further divided into two groups dependent on whether the observed motion depicted forward or backward walking. We find that the effect of the motion stimulus on sensitivity is highly dependent on whether the observed motion is consistent with past experience.     

Differential activation of a central inhibition system by motion and colour distractors

ABSTRACT

The selection of relevant stimuli is partially achieved through inhibition of irrelevant distractors. Using the distractor induced blindness (DIB) paradigm, we investigated whether these inhibitory processes depend on the feature dimension that is used to define distractors. Following a pilot study that found motion and colour targets to be comparably salient, we analysed distractor effects of those two feature dimensions. In both feature dimensions, an inhibition effect depended on the number of distractors. Colour, however, was more sensitive to distractor episodes as compared to motion: The level of inhibition was more pronounced, and its activation required less distractors. The results of a control experiment provided further evidence that, in fact, the feature dimension -instead of design differences between tasks- is responsible for this observation. The dimension-sensitive bias in the activation of a central inhibition system may be attributed to a differential processing of visual signals, depending on their behavioural relevance.     

Temporal perception is enhanced for goal-directed biological actions

ABSTRACT

Research into the visual perception of goal-directed human action indicates that human action perception makes use of specialized processing systems, similar to those that operate in visual expertise. Against this background, the current research investigated whether perception of temporal information in goal-directed human action is enhanced relative to similar motion stimuli. Experiment 1 compared observers’ sensitivity to speed changes in upright human action to a kinematic control (an animation yoked to the motion of the human hand), and also to inverted human action. Experiment 2 compared human action to a non-human motion control (a tool moved the object). In both experiments observers’ sensitivity to detecting the speed changes was higher for the human stimuli relative to the control stimuli, and inversion in Experiment 1 did not alter observers’ sensitivity. Experiment 3 compared observers’ sensitivity to speed changes in goal-directed human and dog actions, in order to determine if enhanced temporal perception is unique to human actions. Results revealed no difference between human and dog stimuli, indicating that enhanced speed perception may exist for any biological motion. Results are discussed with reference to theories of biological motion perception and perception in visual expertise.     

Neural Correlates of Age-related Reduction in Visual Motion Priming

ABSTRACT

Previously we reported that priming of visual motion perception is reduced in older adults compared to younger adults (Jiang, Greenwood, & Parasuraman, 1999 Jiang, Y., Greenwood, P. and Parasuraman, R. 1999. Age-related reduction in 3-D motion priming. Psychology and Aging, 14(4): 619–626.  [Google Scholar], Psychology and Aging, 14(4), 619; Jiang, Luo, & Parasuraman, 2002b Jiang, Y., Luo, Y. J. and Parasuraman, R. 2002b. Two-dimensional visual motion priming is reduced in older adults. Neuropsychology, 16(2): 140–145.  [Google Scholar], Neuropsychology, 16(2), 140). To examine the neural mechanisms underlying this age-related effect, event-related brain potentials (ERPs) were recorded during perceptual judgments of motion directions by younger and older adults in two experiments. When judging single-step motion, both younger and older adults evoked significantly larger ERP late positive component (LPC) responses to unambiguous motion compared to LPC responses elicited by ambiguous motion. In contrast, compared to the younger adults, the older adults evoked comparable but delayed ERP responses to single motion steps. In the second experiment the younger and older groups judged the directions of two successive motion-steps (either motion priming or motion reversals). Under short (200–400 ms) stimulus onset asynchrony (SOA), the difference between the ERP responses to priming and reversal conditions was significantly larger for the younger than for the older adults. This study provides the first electrophysiological evidence that brain aging leads to delayed processing of single motion direction and visual motion priming as early as 100 ms in the early visual cortex. Age-related changes in strength and temporal characteristics of neural responses in temporal-parietal regions were particularly pronounced in older adults when successive motion signals are placed closely in time, within 400 ms.     

Colour and spatial cueing in low-prevalence visual search

People are able to judge the current position of occluded moving objects. This operation is known as motion extrapolation. It has previously been suggested that motion extrapolation is independent of the oculomotor system. Here we revisited this question by measuring eye position while participants completed two types of motion extrapolation task. In one task, a moving visual target travelled rightwards, disappeared, then reappeared further along its trajectory. Participants discriminated correct reappearance times from incorrect (too early or too late) with a two-alternative forced-choice button press. In the second task, the target travelled rightwards behind a visible, rectangular occluder, and participants pressed a button at the time when they judged it should reappear. In both tasks, performance was significantly different under fixation as compared to free eye movement conditions. When eye movements were permitted, eye movements during occlusion were related to participants' judgements. Finally, even when participants were required to fixate, small changes in eye position around fixation (<2°) were influenced by occluded target motion. These results all indicate that overlapping systems control eye movements and judgements on motion extrapolation tasks. This has implications for understanding the mechanism underlying motion extrapolation.     

Induced Rotational Motion With Nonabutting Inducing and Induced Stimuli: Implications Regarding Two Forms of Induced Motion

Induced motion is the illusory motion of a static stimulus in the opposite direction to a moving stimulus. Two types of induced motion have been distinguished: (a) when the moving stimulus is distant from the static stimulus and undergoes overall displacement, and (b) when the moving stimulus is pattern viewed within fixed boundaries that abut the static stimulus. Explanations of the 1st type of induced motion refer to mediating phenomena, such as vection, whereas the 2nd type is attributed to local processing by motion-sensitive neurons. The present research was directed to a display that elicited induced rotational motion with the characteristics of both types of induced motion: the moving stimulus lay within fixed boundaries, but the inducing and induced stimuli were distant from each other. The author investigated the properties that distinguished the two types of induced motion. In 3 experiments, induced motion persisted indefinitely, inter-ocular transfer of the aftereffect of induced motion was limited to about 20%, and the time-course of the aftereffect of induced motion could not be attributed to vection. Those results were consistent with fixed-boundary induced motion. However, they could not be explained by local processing. Instead, the results might reflect the detection of object motion within a complex flow-field that resulted from the observer's motion.     

Concurrent Directional Adaptation of Reactive Saccades and Hand Movements to Target Displacements of Different Size

When eye and hand movements are concurrently aimed at double-step targets that call for equal and opposite changes of response direction (–10° for the eyes, +10° for the hand), adaptive recalibration of both motor systems is strongly attenuated; instead, hand but not eye movements are changed by corrective strategies (V. Grigorova et al., 2013a). The authors introduce a complementary paradigm, where double-step targets call for a –10° change of eye and a ?30° change for hand movements. If compared to control subjects adapting only the eyes or only the hand, adaptive improvements were comparable for the eyes but were twice as large for the hand; in contrast, eye and hand aftereffects were comparable to those in control subjects. The authors concluded that concurrent exposure of eyes and hand to steps of the same direction but different size facilitated hand strategies, but didn't affect recalibration. This finding together with previous one (V. Grigorova et al., 2013a), suggests that concurrent adaptation of eyes and hand reveals different mechanisms of recalibration for step sign and step size, which are shared by reactive saccades and hand movements. However, hand mostly benefits from strategies provoked by the difference in target step sign and size.     

Temporal structure coding with and without awareness

In order to interpret a constantly changing environment, visual events far apart in space and time must be integrated into a unified percept. While spatial properties of invisible signals are known to be encoded without awareness, the fate of temporal properties remains largely unknown. Here, we probed temporal integration for two distinct motion stimuli that were either visible or rendered invisible using continuous flash suppression. We found that when invisible, both the direction of apparent motion and the gender of point-light walkers were processed only when defined across short time periods (i.e., respectively 100 ms and 1000 ms). This limitation was not observed under full visibility. These similar findings at two different hierarchical levels of processing suggest that temporal integration windows shrink in the absence of perceptual awareness. We discuss this phenomenon as a key prediction of the global neuronal workspace and the information integration theories of consciousness.