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Biomedical subjects

P Cavanagh

Publications and source records attributed to P Cavanagh.

At least 37 records · Page 2Linked to original sources
PubMed2000

Motion distorts visual space: shifting the perceived position of remote stationary objects.

To perceive the relative positions of objects in the visual field, the visual system must assign locations to each stimulus. This assignment is determined by the object's retinal position, the direction of gaze, eye movements, and the motion of the object itself. Here we show that perceived location is also influenced by motion signals that originate in distant regions of the visual field. When a pair of stationary lines are flashed, straddling but not overlapping a rotating radial grating, the lines appear displaced in a direction consistent with that of the grating's motion, even when the lines are a substantial distance from the grating. The results indicate that motion's influence on position is not restricted to the moving object itself, and that even the positions of stationary objects are coded by mechanisms that receive input from motion-sensitive neurons.

Humans↗
PubMed2000

Nonlinearity in color space measured by apparent motion.

We used an apparent motion technique to examine the intensity coding along the three cardinal axes of color space: achromatic (L + M + S), L-M cone, and S cone axes. Two horizontal bars of different colors were alternated to produce a vertical displacement. The color of the background was a mixture varied between the colors of the two bars. When the background color was close to either of the test colors, only the bar that was more salient appeared to jump. Observers adjusted the color of the background until they saw either the two bars moved equally frequently or both bars moved at once. If the color difference in a linear cone excitation space controls this apparent motion, the setting should be midway between the two colors. All of the three cardinal axes showed some deviation from linear behavior. The nonlinearity was less extreme than a logarithmic function for both the achromatic and S cone axes and could be attributed to a small compressive nonlinearity, possibly at the level of cone responses. However, the L-M stimuli showed a more extreme departure from linearity, which suggested a nonlinearity at an opponent site. A test of perceived contrast judgments did not show this nonlinearity for L-M axis, suggesting that it is specific to the L-M contribution to apparent motion.

Color Perception↗
PubMed1999

Position-based motion perception for color and texture stimuli: effects of contrast and speed.

Motion can be perceived either through low-level, motion-energy detection or through tracking the change in position of features. Previously we have shown that, while luminance-based motion likely is detected with velocity-sensitive motion-energy units, patterns defined by texture or binocular disparity ('second-order' stimuli) were tracked by a position-sensitive mechanism (Seiffert & Cavanagh (1998) Vision Research, 38, 3569-3582). Here, we use the same technique, measuring motion amplitude thresholds of oscillating gratings over a range of temporal frequencies and find that the motion of low-contrast equiluminant red/green gratings is also detected with position tracking. In addition, we find that as contrast or speed increases these results change: high-contrast or high-speed equiluminant color or texture-based motion is detected by velocity-sensitive mechanisms. These results help resolve the dispute over the processes which detect the motion of non-luminance based stimuli. Both systems are available, but their relative efficiency changes as a function of contrast and speed. A position-tracking process is more sensitive at low contrasts and low speeds whereas a motion-energy system is more sensitive at high contrasts and high speeds.

Color Perception↗
PubMed1998

A jitter after-effect reveals motion-based stabilization of vision.

A shaky hand holding a video camera invariably turns a treasured moment into an annoying, jittery momento. More recent consumer cameras thoughtfully offer stabilization mechanisms to compensate for our unsteady grip. Our eyes face a similar challenge in that they are constantly making small movements even when we try to maintain a fixed gaze. What should be substantial, distracting jitter passes completely unseen. Position changes from large eye movements (saccades) seem to be corrected on the basis of extraretinal signals such as the motor commands sent to the eye muscle, and the resulting motion responses seem to be simply switched off. But this approach is impracticable for incessant, small displacements, and here we describe a novel visual illusion that reveals a compensation mechanism based on visual motion signals. Observers were adapted to a patch of dynamic random noise and then viewed a larger pattern of static random noise. The static noise in the unadapted regions then appeared to 'jitter' coherently in random directions. Several observations indicate that this visual jitter directly reflects fixational eye movements. We propose a model that accounts for this illusion as well as the stability of the visual world during small and/or slow eye movements such as fixational drift, smooth pursuit and low-amplitude mechanical vibrations of the eyes.

Adaptation, Ocular↗
PubMed1998

Recovery of 3D volume from 2-tone images of novel objects.

In 2-tone images (e.g., Dallenbach's cow), only two levels of brightness are used to convey image structure-dark object regions and shadows are turned to black and light regions are light regions are turned white. Despite a lack of shading, hue and texture information, many 2-tone images of familiar objects and scenes are accurately interpreted, even by naive observers. Objects frequently appear fully volumetric and are distinct from their shadows. If perceptual interpretation of 2-tone images is accomplished via bottom-up processes on the basis of geometrical structure projected to the image (e.g., volumetric parts, contour and junction information) novel objects should appear volumetric as readily as their familiar counterparts. We demonstrate that accurate volumetric representations are rarely extracted from 2-tone images of novel objects, even when these objects are constructed from volumetric primitives such as generalized cones (Marr, D., Nishihara, H.K., 1978. Proceedings of the Royal Society London 200, 269-294; Biederman, I. 1985. Computer Vision, Graphics, and Image Processing 32, 29-73), or from the rearranged components of a familiar object which is itself recognizable as a 2-tone image. Even familiar volumes such as canonical bricks and cylinders require scenes with redundant structure (e.g., rows of cylinders) or explicit lighting (a lamp in the image) for recovery of global volumetric shape. We conclude that 2-tone image perception is not mediated by bottom-up extraction of geometrical features such as junctions or volumetric parts, but may rely on previously stored representations in memory and a model of the illumination of the scene. The success of this top-down strategy implies it is available for general object recognition in natural scenes.

Adult↗
PubMed1998

Optomotor test for wavelength sensitivity in guppyfish (Poecilia reticulata).

Wavelength sensitivity was measured in the guppyfish by means of optomotor responses to a special apparent-motion display. A set of red and green bars appeared to humans to move to the left if red was darker than green, but to the right if red was lighter than green. At equiluminance there was no apparent motion. By noting the direction in which the fish swam to follow the stripes we were able to record equiluminance points for red, green and blue. Store-bought guppies (Poecilia reticulata) were mildly protan compared with humans, and wild-strain guppies were strongly protan, being 50% more sensitive to short wavelengths and 67% more sensitive to medium wavelengths than human observers. We also measured optomotor responses to achromatic Michelson contrast: responses were maximum if the contrast exceeded 0.3. Finally, the optomotor threshold (signal/noise ratio) for motion coherence was 20% for fine dots and 40% for coarse dots. These stimuli should be easy to use on any non-verbal species.

Animals↗
PubMed1998

Position displacement, not velocity, is the cue to motion detection of second-order stimuli.

Motion detection can be achieved either with mechanisms sensitive to a target's velocity, or sensitive to change in a target's position. Using a procedure to dissociate these two provided by Nakayama and Tyler (Vis Res 1981;21:427-433), we explored detection of first-order (luminance-based) and various second-order (texture-based and stereo-based) motion. In the first experiment, observers viewed annular gratings oscillating in rotational motion at various rates. For each oscillation temporal frequency, we determined the minimum displacement of the pattern for which observers could reliably see motion. For first-order motion, these motion detection thresholds decreased with increasing temporal frequency, and thus were determined by a minimum velocity. In contrast, motion detection thresholds for second-order motion remained roughly constant across temporal frequency, and thus were determined by a minimum displacement. In Experiment 2, luminance-based gratings of different contrasts were tested to show that the velocity-dependence was not an artifact of pattern visibility. In the remaining experiments, results similar to Experiment 1 were obtained with a central presentation of a linear grating, instead of an annular grating (Experiment 3), and with a motion discrimination (phase discrimination) rather than motion detection task (Experiment 4). We conclude that, within the ranges tested here, second-order motion is more readily detected with a mechanism which tracks the change of position of features over time.

Contrast Sensitivity↗
PubMed1998

A shape-contrast effect for briefly presented stimuli.

When a suprathreshold visual stimulus is flashed for 60-300 ms and masked, though it is no longer visibly degraded, the perceived shape is vulnerable to distortion effects, especially when a 2nd shape is present. Specifically, when preceded by a flashed line, a briefly flashed circle appears to be an ellipse elongated perpendicular to the line. Given an appropriate stimulus onset asynchrony, this distortion is perceived when the 2 stimuli (approximately 4 degrees) are presented as far as 12 degrees apart but is not due to perception of apparent motion between the 2 stimuli. Additional pairs of shapes defined by taper and overall curvature also revealed similar nonlocal shape distortion effects. The test shapes always appeared to be more dissimilar to the priming shapes, a distortion termed a shape-contrast effect. Its properties are consistent with the response characteristics of the shape-tuned neurons in the inferotemporal cortex and may reveal the underlying dimensions of early shape encoding.

Adult↗
PubMed1998

Retinotopy and color sensitivity in human visual cortical area V8.

Prior studies suggest the presence of a color-selective area in the inferior occipital-temporal region of human visual cortex. It has been proposed that this human area is homologous to macaque area V4, which is arguably color selective, but this has never been tested directly. To test this model, we compared the location of the human color-selective region to the retinotopic area boundaries in the same subjects, using functional magnetic resonance imaging (fMRI), cortical flattening and retinotopic mapping techniques. The human color-selective region did not match the location of area V4 (neither its dorsal nor ventral subdivisions), as extrapolated from macaque maps. Instead this region coincides with a new retinotopic area that we call 'V8', which includes a distinct representation of the fovea and both upper and lower visual fields. We also tested the response to stimuli that produce color afterimages and found that these stimuli, like real colors, caused preferential activation of V8 but not V4.

Afterimage↗
PubMed1998

Complete sparing of high-contrast color input to motion perception in cortical color blindness.

It is widely held that color and motion are processed by separate parallel pathways in the visual system, but this view is difficult to reconcile with the fact that motion can be detected in equiluminant stimuli that are defined by color alone. To examine the relationship between color and motion, we tested three patients who had lost their color vision following cortical damage (central achromatopsia). Despite their profound loss in the subjective experience of color and their inability to detect the motion of faint colors, all three subjects showed surprisingly strong responses to high-contrast, moving color stimuli--equal in all respects to the performance of subjects with normal color vision. The pathway from opponent-color detectors in the retina to the motion analysis areas must therefore be independent of the damaged color centers in the occipitotemporal area. It is probably also independent of the motion analysis area MT/V5, because the contribution of color to motion detection in these patients is much stronger than the color response of monkey area MT.

Adult↗
PubMed1998

Cortical fMRI activation produced by attentive tracking of moving targets.

Attention can be used to keep track of moving items, particularly when there are multiple targets of interest that cannot all be followed with eye movements. Functional magnetic resonance imaging (fMRI) was used to investigate cortical regions involved in attentive tracking. Cortical flattening techniques facilitated within-subject comparisons of activation produced by attentive tracking, visual motion, discrete attention shifts, and eye movements. In the main task, subjects viewed a display of nine green "bouncing balls" and used attention to mentally track a subset of them while fixating. At the start of each attentive-tracking condition, several target balls (e.g., 3/9) turned red for 2 s and then reverted to green. Subjects then used attention to keep track of the previously indicated targets, which were otherwise indistinguishable from the nontargets. Attentive-tracking conditions alternated with passive viewing of the same display when no targets had been indicated. Subjects were pretested with an eye-movement monitor to ensure they could perform the task accurately while fixating. For seven subjects, functional activation was superimposed on each individual's cortically unfolded surface. Comparisons between attentive tracking and passive viewing revealed bilateral activation in parietal cortex (intraparietal sulcus, postcentral sulcus, superior parietal lobule, and precuneus), frontal cortex (frontal eye fields and precentral sulcus), and the MT complex (including motion-selective areas MT and MST). Attentional enhancement was absent in early visual areas and weak in the MT complex. However, in parietal and frontal areas, the signal change produced by the moving stimuli was more than doubled when items were tracked attentively. Comparisons between attentive tracking and attention shifting revealed essentially identical activation patterns that differed only in the magnitude of activation. This suggests that parietal cortex is involved not only in discrete shifts of attention between objects at different spatial locations but also in continuous "attentional pursuit" of moving objects. Attentive-tracking activation patterns were also similar, though not identical, to those produced by eye movements. Taken together, these results suggest that attentive tracking is mediated by a network of areas that includes parietal and frontal regions responsible for attention shifts and eye movements and the MT complex, thought to be responsible for motion perception. These results are consistent with theoretical models of attentive tracking as an attentional process that assigns spatial tags to targets and registers changes in their position, generating a high-level percept of apparent motion.

Adult↗
PubMed1997

Focused attention distorts visual space: an attentional repulsion effect.

Attention was focused at a specific location either by a briefly flashed cue (cue-induced attention) or by a voluntary effort (voluntary attention). In both cases, briefly presented probes appeared displaced away from the focus of attention. The results showed that the effect of cue-induced attention was transient whereas the effect of voluntary attention was long lasting. The repulsion effect was most evident with brief probe durations (< 200 ms). Control experiments ruled out nonattentional hypotheses based on classic figural aftereffects and apparent motion. Although a number of studies have demonstrated enhancements of visual perception at attended locations, the present studies show that focused attention can distort the encoding of nearby positions. Speculation is offered that the repulsion effect is one of the costs involved in the allocation of more resources to the focus of attention.

Attention↗
PubMed1996

Attentional resolution and the locus of visual awareness.

Visual spatial resolution is limited by factors ranging from optics to neuronal filters in the visual cortex, but it is not known to what extent it is also limited by the resolving power of attention. To investigate this, we studied adaptation to lines of specific orientation, a process that occurs in primary visual cortex. When a single grating is presented in the periphery of the visual field, human observers are aware of its orientation, but when it is flanked by other similar gratings ('crowding'), its orientation becomes impossible to discern. Nevertheless, we show that orientation-specific adaptation is not affected by crowding, implying that spatial resolution is limited by an attentional filter acting beyond the primary visual cortex. Consistent with this, we find that attentional resolution is greater in the lower than in the upper visual field, whereas there is no corresponding asymmetry in the primary visual cortex. We suggest that the attentional filter acts in one or more higher visual cortical areas to restrict the availability of visual information to conscious awareness.

Adaptation, Physiological↗
PubMed1996

Localizing contours defined by more than one attribute.

Two experiments were run in order to test how information from different attributes is combined to localize contours. In Expt 1 the apparent position of a contour defined by one attribute was measured while a contour defined by another attribute was presented beside it. Interactions were found between all pairings of luminance, color, motion and texture. These results suggested that the information associated with each contour is integrated at a common site. In Expt 2 the precision of localization was measured for contours defined by one, two or three attributes (combinations of luminance, color and texture). The improvement in precision with additional attributes again supported an integration of contour information at a common site prior to a decision of localization.

Color Perception↗
PubMed1996

Texture laciness: the texture equivalent of transparency?

Displays with overlapping squares of different textures were produced. In some texture combinations, the overlapping area appears to be a new texture. In other combinations, however, one texture is seen through the other as if it were inscribed on a transparent sheet and held in front of the other. This phenomenon can be called texture laciness. It is claimed that texture laciness is important because in the natural world we frequently encounter overlapping textures that we perceive as separate. In examining the conditions that lead to texture laciness, it was found that (1) laciness occurs more strongly with decreasing similarity between elements of two textures, (2) when the elements of the two textures are the same, the overlapped area tends to appear as a new texture, and (3) the physical overlapping of the individual elements of two textures hinders texture decomposition, irrespective of relative positioning. It is suggested that the textures inducing laciness may be processed as surfaces rather than just collections of identical elements. Texture laciness also reveals that even if 'antitextons'-the shapes of the spaces between texture elements, which have been regarded as important in texture discrimination-are destroyed by positioning another set of texture elements in the spaces, the textures can remain sufficiently identifiable to be perceived as separate.

Adult↗