Predicting the motion after-effect from sensitivity loss.
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The widely accepted disinhibition theory of the motion after-effect (MAE) proposes that the balance point of an opponent mechanism is changed by directional adaptation. To see if the post-adaptation balance point could be predicted from contrast adaptation, we measured threshold-vs-contrast (i.e., T-vs-C or dipper) functions, before and after adaptation to moving gratings. For test stimuli moving in the same direction, adaptation shifted the point of maximum facilitation (i.e., the dip) upwards and rightwards. For tests moving in the opposite direction, adaptation produced a similar, but smaller, shift. These shifts are consistent with a change in divisive gain control. They are also consistent with subtractive inhibition followed by half-wave rectification. We attempted to use transducer functions derived from these data to predict the strength of the MAE. When combined, gratings moving in the adapted and opposite directions appeared perfectly balanced (i.e., counterphasing) when the latter was given approximately 2% more contrast than was predicted on the basis of the derived transducers. This small under-prediction may be indicative of sensory recalibration. Finally, we found that adaptation did not alter the fact that low-contrast stimuli could be detected and their direction identified with similar accuracy. We conclude that both static and dynamic forms of MAE are primarily caused by a decreased sensitivity in directionally tuned mechanisms, as proposed by the disinhibition theory. (+info)
Local and global motion after-effects are both enhanced in migraine, and the underlying mechanisms differ across cortical areas.
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Visual after-effects are illusions that occur after prolonged viewing of visual displays (pattern adaptation). The motion after-effect (MAE), for example, is an illusory impression of motion that is seen after viewing moving displays. After-effects have been used extensively in basic vision research as well as in clinical settings, and have been reported to be enhanced in migraine. Pattern adaptation is a cortical phenomenon that reflects both cellular mechanisms acting within individual neurons and specific interactions between groups of neurons activated by the adapting display. A remarkable feature of the MAE is that its duration is only slightly reduced if a delay is inserted between the end of the adaptation and the test display ('storage'). The reduction is consistent with recovery of the cellular component, and the residual with network changes that are maintained during the delay. This study aimed (i) to assess explanations for prolonged MAEs in migraine by teasing apart the proposed cellular and network components of adaptation using storage; (ii) to determine the extent of cortical abnormality in migraine using local and global MAEs, which reflect adaptation at different stages of the visual system. Fifty migraine (22 with, 28 without aura) and 50 control participants adapted to motion before viewing a stationary or dynamic (random motion) test, which consequently appeared to move in the opposite direction (local and global MAEs, respectively). Half of the trials included a delay between the adapting and test displays. The results extend those reported previously, as both local and global MAEs lasted longer in migraine compared with the control group. Global MAEs survived delays almost completely for both groups, whereas local MAEs were reduced to a greater extent in migraine. There were no significant differences between migraine subgroups classified according to the presence or absence of visual aura. These results suggest that cellular recovery is slowed in migraine for early but not later visual cortical areas. Sustained network changes following adaptation are implicated across cortical areas. Differences between people with and without migraine on various measures of visual perception have been attributed to abnormal cortical processing in migraine, variously described by hyperexcitability, heightened responsiveness and/or a lack of intra-cortical inhibition. The results are not consistent with hyperexcitability resulting from a lack of inhibition in migraine, but are consistent with extended suppression of intra-cortical excitation. The implications of these results for alternative models of hyperexcitability are discussed. (+info)
A moving stimulus is normally required to elicit smooth pursuit eye movements that serve to keep the retinal image of moving objects on the fovea. Recent experiments have shown that in cases where motion cues are ambiguous, pursuit eye movements tend to agree in direction and speed with the percept of motion. Here, we exploit the motion aftereffect (MAE) to show for the first time that smooth pursuit eye movements can also be elicited by the illusory motion of a stationary stimulus. After prolonged exposure to a moving stimulus, subjects show reliable pursuit of a physically stationary stimulus that is perceived to be moving. Conversely, the eyes remain stationary when viewing a physically moving stimulus that is perceived to be stationary. The MAE biases smooth eye movements in a way that agrees with the constant offset that is required to null the MAE perceptually. The agreement between perception and pursuit holds over a variety of stimulus conditions that modulate the magnitude of the MAE. (+info)
Adaptation aftereffects in the perception of gender from biological motion.
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Human visual perception is highly adaptive. While this has been known and studied for a long time in domains such as color vision, motion perception, or the processing of spatial frequency, a number of more recent studies have shown that adaptation and adaptation aftereffects also occur in high-level visual domains like shape perception and face recognition. Here, we present data that demonstrate a pronounced aftereffect in response to adaptation to the perceived gender of biological motion point-light walkers. A walker that is perceived to be ambiguous in gender under neutral adaptation appears to be male after adaptation with an exaggerated female walker and female after adaptation with an exaggerated male walker. We discuss this adaptation aftereffect as a tool to characterize and probe the mechanisms underlying biological motion perception. (+info)
Fractal rotation isolates mechanisms for form-dependent motion in human vision.
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Here, we describe a motion stimulus in which the quality of rotation is fractal. This makes its motion unavailable to the translation-based motion analysis known to underlie much of our motion perception. In contrast, normal rotation can be extracted through the aggregation of the outputs of translational mechanisms. Neural adaptation of these translation-based motion mechanisms is thought to drive the motion after-effect, a phenomenon in which prolonged viewing of motion in one direction leads to a percept of motion in the opposite direction. We measured the motion after-effects induced in static and moving stimuli by fractal rotation. The after-effects found were an order of magnitude smaller than those elicited by normal rotation. Our findings suggest that the analysis of fractal rotation involves different neural processes than those for standard translational motion. Given that the percept of motion elicited by fractal rotation is a clear example of motion derived from form analysis, we propose that the extraction of fractal rotation may reflect the operation of a general mechanism for inferring motion from changes in form. (+info)
Filtering items of mass distraction: top-down biases against distractors are necessary for the feature-based carry-over to occur.
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In preview search a new target is difficult to detect if it carries a feature shared with the old distractors [Braithwaite, J. J., Humphreys, G. W., & Hodsoll, J. (2003). Color grouping in space and time: Evidence from negative color-based carry-over effects in preview search. Journal of Experimental Psychology: Human Perception and Performance, 29(4), 758-778.] Two experiments are presented which examined whether this negative color carry-over effect is dependent on an attentional-set to ignore old, irrelevant distractors. Consistent with this, the data show that the negative carry-over effect is greatly reduced if the attentional-set to ignore the old preview items is removed and replaced by a set to prioritize the old items instead. The findings demonstrate that preview search, and the carry-over effect, are at least partly determined by a top-down intentional bias against old, irrelevant information. (+info)
The cyclopean illusion unleashed.
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The cyclopean illusion is the apparent lateral shift of stationary stimuli on a visual axis that occurs when vergence changes. This illusion is predictable from the rules of visual direction. There are three stimulus situations reported in the literature, however, in which the illusion does not occur. In the three experiments reported here we examine those stimulus situations. Experiment 1 showed that an afterimage seen on a stimulus moving on the visual axis does not produce the illusion as reported in the literature but an afterimage seen on a screen does. Experiment 2 showed that the illusion occurs for an intermittently presented stimulus in contrast to what has been reported previously. Experiment 3 showed that a monocular stimulus presented against a random-dot background produced the illusion, also in contrast to what has been reported. The results were consistent with the rules of visual direction. (+info)
Turning the other cheek: the viewpoint dependence of facial expression after-effects.
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How do we visually encode facial expressions? Is this done by viewpoint-dependent mechanisms representing facial expressions as two-dimensional templates or do we build more complex viewpoint independent three-dimensional representations? Recent facial adaptation techniques offer a powerful way to address these questions. Prolonged viewing of a stimulus (adaptation) changes the perception of subsequently viewed stimuli (an after-effect). Adaptation to a particular attribute is believed to target those neural mechanisms encoding that attribute. We gathered images of facial expressions taken simultaneously from five different viewpoints evenly spread from the three-quarter leftward to the three-quarter rightward facing view. We measured the strength of expression after-effects as a function of the difference between adaptation and test viewpoints. Our data show that, although there is a decrease in after-effect over test viewpoint, there remains a substantial after-effect when adapt and test are at differing three-quarter views. We take these results to indicate that neural systems encoding facial expressions contain a mixture of viewpoint-dependent and viewpoint-independent elements. This accords with evidence from single cell recording studies in macaque and is consonant with a view in which viewpoint-independent expression encoding arises from a combination of view-dependent expression-sensitive responses. (+info)