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Lee A Gilroy

Publications and source records attributed to Lee A Gilroy.

11 recordsLinked to original sources

Spatial grouping in human vision: temporal structure trumps temporal synchrony.

Temporal information promotes visual grouping of local image features into global spatial form. However, experiments demonstrating time-based grouping typically confound two potential sources of information: temporal synchrony (precise timing of changes) and temporal structure (pattern of changes over time). Here, we show that observers prefer temporal structure for determining perceptual organization. That is, human vision groups elements that change according to the same global pattern, even if the changes themselves are not synchronous. This finding prompts an important, testable prediction concerning the neural mechanisms of binding: patterns of neural spiking over time may be more important than absolute spike synchrony.

Cues↗

Depth of interocular suppression associated with continuous flash suppression, flash suppression, and binocular rivalry.

When conflicting images are presented to the corresponding regions of the two eyes, only one image may be consciously perceived. In binocular rivalry (BR), two images alternate in phenomenal visibility; even a salient image is eventually suppressed by an image of low saliency. Recently, N. Tsuchiya and C. Koch (2005) reported a technique called continuous flash suppression (CFS), extending the suppression duration more than 10-fold. Here, we investigated the depth of this prolonged form of interocular suppression as well as conventional BR and flash suppression (FS) using a probe detection task. Compared to monocular viewing condition, CFS elevated detection thresholds more than 20-fold, whereas BR did so by 3-fold. In subsequent experiments, we dissected CFS into several components. By manipulating the number and timing of flashes with respect to the probe, we found that the stronger suppression in CFS is not due to summation between BR and FS but is caused by the summation of the suppression due to multiple flashes. Our results support the view that CFS is not a stronger version of BR but is due to the accumulated suppressive effects of multiple flashes.

Humans↗

The interaction between binocular rivalry and negative afterimages.

Afterimage formation, historically attributed to retinal mechanisms, may also involve postretinal process. Consistent with this notion are results from experiments, reported here, investigating the interaction between binocular rivalry and negative afterimages (AIs). In Experiment 1, one eye was exposed to a grating never consciously experienced by the observer because this grating remained suppressed in rivalry throughout induction (the exclusively dominant stimulus was designed to preclude formation of an AI). As expected, the suppressed grating generated a vivid AI whose orientation could be accurately identified; not surprisingly, the strength of this AI varied with induction contrast. Experiment 2 revealed, however, that the strength of this AI produced during suppression was significantly weaker than the AI produced by that same stimulus when it was visible throughout the entire induction period, implying that some component of AI induction is susceptible to interocular suppression. In Experiment 3, AIs of dichoptic, orthogonally oriented gratings were induced in a way ensuring that one of the two gratings was exclusively dominant during the induction period. Dissimilar monocular AIs engaged in rivalry, as expected, but, surprisingly, the AI induced by the suppressed grating initially dominated. We offer two alternative accounts of this counterintuitive finding, both based on differential neural adaptation.

Adaptation, Ocular↗

A common mechanism for the perception of first-order and second-order apparent motion.

A common mechanism for perceiving first-order, luminance-defined, and second-order, texture-contrast defined apparent motion between two element locations is indicated by: (1) transitivity--whether or not motion is perceived is inter-changeably affected by activationally equivalent luminance and contrast changes at each location, (2) local integration--whether or not motion is perceived depends on the net activation change resulting from simultaneous background-relative luminance and background-relative contrast changes at the same element location, and (3) inseparability--apparent motion is not perceived through independent first- or second-order mechanisms when luminance and contrast co-vary at the same location. These results, which are predicted by the response characteristics of directionally selective cells in areas V1, MT, and MST, are not instead attributable to changes in the location of the most salient element (third-order motion), attentive feature tracking, or artifactual first-order motion. Their inconsistency with Lu and Sperling's [Lu, Z., Sperling, G. (1995a). Attention-generated apparent motion. Nature 377, 237, Lu, Z., Sperling, G. (2001). Three-systems theory of human visual motion perception: review and update. Journal of the Optical Society of America A 18, 2331] model, which specifies independent first- and second-order mechanisms, may be due to computational requirements particular to the motion of discrete objects with distinct boundaries defined by spatial differences in luminance, texture contrast, or both.

Contrast Sensitivity↗

Mixed messengers, unified message: spatial grouping from temporal structure.

In dynamic visual environments, objects can differ from their backgrounds in terms of their associated temporal structure--the time course of changes in some stimulus property defining object and background. In a series of experiments, we investigated whether different "messengers" of temporal structure group into coherent spatial forms. Observers viewed arrays of Gabor patches in which different temporal structures designated figure and ground regions; extracting the figure required grouping across synchronized orientation, spatial frequency, phase, and/or contrast changes. Observers were able to extract spatial form from temporal structure even when information had to be combined across different messengers. Further, mixing messengers of temporal structure proved cost-free: task performance when grouping across messengers approximated performance when all information resided within a single messenger. Thus, the visual system can abstract temporal structure regardless of the messenger of the dynamic event; a coherent spatial structure emerges from this abstracted temporal structure.

Artifacts↗

Hearing what the eyes see: auditory encoding of visual temporal sequences.

When the senses deliver conflicting information, vision dominates spatial processing, and audition dominates temporal processing. We asked whether this sensory specialization results in cross-modal encoding of unisensory input into the task-appropriate modality. Specifically, we investigated whether visually portrayed temporal structure receives automatic, obligatory encoding in the auditory domain. In three experiments, observers judged whether the changes in two successive visual sequences followed the same or different rhythms. We assessed temporal representations by measuring the extent to which both task-irrelevant auditory information and task-irrelevant visual information interfered with rhythm discrimination. Incongruent auditory information significantly disrupted task performance, particularly when presented during encoding; by contrast, varying the nature of the rhythm-depicting visual changes had minimal impact on performance. Evidently, the perceptual system automatically and obligatorily abstracts temporal structure from its visual form and represents this structure using an auditory code, resulting in the experience of "hearing visual rhythms."

Acoustic Stimulation↗

Physics embedded in visual perception of three-dimensional shape from motion.

Visual perception, and by implication underlying neural events, can become unstable when optical information specifying objects is ambiguous. Here we report that one striking form of instability-perceived three-dimensional structure-from-motion (SFM)-can be stabilized when an otherwise ambiguous object appears within a context implying frictional interactions with another rotating object; violations of physical conditions specifying friction disrupt stabilization. Evidently, information about frictional interaction is embedded within neural mechanisms specifying SFM.

Humans↗

Multiplicative nonlinearity in the perception of apparent motion.

Evidence is reported indicating that the perception of apparent motion is better predicted by the multiplicative combination of luminance changes at two element locations than by the sum or squared-sum of the luminance changes, or by the motion energy in the stimulus. Because the results were obtained with a stimulus for which motion was specified by simultaneous luminance changes, they support a Reichardt-style motion detector model, but without the asymmetrical delay specified by current versions. Motion direction in the modified model relies on asymmetrical stimulus information rather than asymmetrical delay. That is, one subunit of the detector responds to changes in luminance toward the background luminance (the start of the motion path), and the other to changes in luminance away from the background luminance (the end of the motion path).

Fourier Analysis↗

Detection of counter-changing contrast: second-order apparent motion without postrectification motion-energy analysis or salience mapping/feature tracking.

The perception of 2nd-order, texture-contrast-defined motion was studied for apparent-motion stimuli composed of a pair of spatially displaced, simultaneously visible checkerboards. It was found that background-relative, counter-changing contrast provided the informational basis for the perception of 2nd-order apparent motion; motion began where contrast changed toward the contrast value of the background checkerboard and ended where contrast changed away from the background value. The perceived apparent motion was not attributable to either postrectification motion-energy analysis or salience-mapping/feature-tracking mechanisms. Parallel results for 1st-order, luminance-defined motion (H. S. Hock, L. A. Gilroy, & G. Harnett, 2002) suggest that counter-changing activation provides a common basis for the perception of both luminance- and texture-contrast-defined apparent motion.

Humans↗

Visual motion retards alternations between conflicting perceptual interpretations.

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.

Humans↗

Perceptual consequences of centre-surround antagonism in visual motion processing.

Centre-surround receptive field organization is a ubiquitous property in mammalian visual systems, presumably tailored for extracting image features that are differentially distributed over space. In visual motion, this is evident as antagonistic interactions between centre and surround regions of the receptive fields of many direction-selective neurons in visual cortex. In a series of psychophysical experiments we make the counterintuitive observation that increasing the size of a high-contrast moving pattern renders its direction of motion more difficult to perceive and reduces its effectiveness as an adaptation stimulus. We propose that this is a perceptual correlate of centre-surround antagonism, possibly within a population of neurons in the middle temporal visual area. The spatial antagonism of motion signals observed at high contrast gives way to spatial summation as contrast decreases. Evidently, integration of motion signals over space depends crucially on the visibility of those signals, thereby allowing the visual system to register motion information efficiently and adaptively.

Contrast Sensitivity↗