We measured visual-adaptation strength under variations in visual awareness by manipulating phenomenal invisibility of adapting stimuli using binocular rivalry and visual crowding. Results showed that the threshold-elevation aftereffect and the translational motion aftereffect were reduced substantially during binocular rivalry and crowding. Importantly, aftereffect reduction was correlated with the proportion of time that the adapting stimulus was removed from visual awareness. These findings indicate that the neural events that underlie both rivalry and crowding are inaugurated at an early stage of visual processing, because both the threshold-elevation aftereffect and translational motion aftereffect arise, at least in part, from adaptation at the earliest stages of cortical processing. Also, our findings make it necessary to reinterpret previous studies whose results were construed as psychophysical evidence against the direct role of neurons in the primary visual cortex in visual awareness. binocular rivalry ͉ crowding ͉ vision V isual adaptation has been dubbed the psychologist's microelectrode (1) because the resulting visual aftereffects presumably reveal response properties of neural mechanisms that are activated by adapting stimuli. Also, measuring visual adaptation under visual conditions that render the adapting stimulus invisible allows one to draw inferences about the neural concomitants of the conditions that produce stimulus invisibility. Specifically, a result showing a full-strength aftereffect that is generated by an invisible stimulus implies normal, unperturbed neural activation at the site of adaptation. This outcome implies that the neural correlates of the visual phenomenon that are used to render the adapting stimulus invisible lie beyond the neural mechanisms that are responsible for the aftereffect. This line of reasoning has been applied to the study of binocular rivalry and visual crowding, which are two extensively studied visual phenomena that are used to ''erase'' visual stimuli from awareness (2). The results have shown that full-strength pattern and motion aftereffects (MAEs) can be induced even when the high-contrast inducing stimuli were absent from awareness for a substantial portion of the adaptation period during binocular rivalry (3-7) and crowding (8, 9). Because adaptation producing these aftereffects includes neural events that presumably occur within cortical areas ranging from the primary visual cortex (V1) (10-12) to the middle-temporal visual area (12, 13), these psychophysical findings have reasonably been interpreted as evidence for the high-level origin of both rivalry (14, 15) and crowding (8,14). Also, these same results were regarded by some workers as key psychophysical evidence against the direct involvement of V1 neurons in conscious visual awareness (16)(17)(18)(19). Measurement of full-strength aftereffects under conditions of rivalry and crowding shows a clear dissociation between the abolished perceptual awareness of the adapting stimulus and unperturbe...
Ambiguous visual information often produces unstable visual perception. In four psychophysical experiments, we found that unambiguous tactile information about the direction of rotation of a globe whose three-dimensional structure is ambiguous significantly influences visual perception of the globe. This disambiguation of vision by touch occurs only when the two modalities are stimulated concurrently, however. Using functional magnetic resonance imaging, we discovered that touching the rotating globe, even when not looking at it, reliably activates the middle temporal visual area (MT+), a brain region commonly thought to be crucially involved in registering structure from motion. Considered together, our results show that the brain draws on somatosensory information to resolve visual conflict.
When the visual system is faced with conflicting or ambiguous stimulus information, visual perception fluctuates over time. We found that perceptual alternations are slowed when inducing stimuli move within the visual field, constantly engaging fresh, unadapted neural tissue. During binocular rivalry, dominance durations were longer when rival figures moved compared to when they were stationary, yielding lower alternation rates. Rate was not reduced, however, when observers tracked the moving targets, keeping the images on approximately the same retinal area. Alternations were reliably triggered when rival targets passed through a local region of the visual field preadapted to one of the rival targets. During viewing of a kinetic globe whose direction of rotation was ambiguous, observers experienced fewer alternations in perceived direction when the globe moved around the visual field or when the globe's axis of rotation changed continuously. Evidently, local neural adaptation is a key ingredient in the instability of perception.
In some cases, the search for a conjunction target proceeds through the smaller group of elements in a display, whereas in others, search is limited to those elements that share a particular feature with the target. In 6 experiments, participants searched for a conjunction target among displays consisting of various proportions of 2 distractor types. Smaller-group search was more prevalent than target-feature search with denser displays and with features that were highly discriminable. Explicit instructions to limit search to a specific feature affected performance only when the discriminability of the guiding feature was much greater than the other target feature. Together, these experiments show that bottom-up factors have more influence in guiding conjunction searches than previously thought.
Variations in the predominance of an object engaged in binocular rivalry may arise from variations in the durations of dominance phases, suppression phases, or both. Earlier work has shown that the predominance of a binocular rival target is enhanced if that target fits well-via common color, orientation, or motion-with its surrounding objects. In the present experiments, the global context outside of the region of rivalry was changed during rivalry, to learn whether contextual information alters the ability to detect changes in a suppressed target itself. Results indicate that context will maintain the dominance of a rival target, but will not encourage a suppressed target to escape from suppression. Evidently, the fate of the suppressed stimulus is determined by neural events distinct from those responsible for global organization during dominance. To reconcile diverse findings concerning rivalry, it may be important to distinguish between processes responsible for selection of one eye's input for dominance from processes responsible for the implementation and maintenance of suppression.
No abstract
The size congruity effect refers to the interaction between the numerical and physical (i.e., font) sizes of digits in a numerical (or physical) magnitude selection task. Although various accounts of the size congruity effect have attributed this interaction to either an early representational stage or a late decision stage, only Risko, Maloney, and Fugelsang (Attention, Perception, & Psychophysics, 75, 1137-1147) have asserted a central role for attention. In the present study, we used a visual search paradigm to further study the role of attention in the size congruity effect. In Experiments 1 and 2, we showed that manipulating top-down attention (via the task instructions) had a significant impact on the size congruity effect. The interaction between numerical and physical size was larger for numerical size comparison (Exp. 1) than for physical size comparison (Exp. 2). In the remaining experiments, we boosted the feature salience by using a unique target color (Exp. 3) or by increasing the display density by using threedigit numerals (Exps. 4 and 5). As expected, a color singleton target abolished the size congruity effect. Searching for threedigit targets based on numerical size (Exp. 4) resulted in a large size congruity effect, but search based on physical size (Exp. 5) abolished the effect. Our results reveal a substantial role for top-down attention in the size congruity effect, which we interpreted as support for a shared-decision account.
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