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Biomedical subjects

K R Gegenfurtner

Publications and source records attributed to K R Gegenfurtner.

At least 19 recordsLinked to original sources
PubMed2005

Illusion effects on grasping are temporally constant not dynamic.

The authors tested whether the effects of the Ebbinghaus illusion on grasping are corrected during late phases of the movement. Surprisingly, the grasp aperture was corrected neither under no-vision (N = 52) nor under full-vision (N = 48) conditions. The authors show that previous reports of a correction (e.g., S. Glover & P. Dixon, 2002a) are due to 2 artifacts: (a) inclusion of time points at which the target object was already touched and (b) erroneous statistics. This removes the central evidence on which S. Glover and P. Dixon's (2001a) planning-control model of action is based. In addition, the authors' results can help to refine more classic notions of motor control (e.g., R. Woodworth, 1899). In consequence, the authors reject S. Glover and P. Dixon's (2001a) planning-control model but not classic online-control theories.

Adolescent↗
PubMed2001

Detection of animals in natural images using far peripheral vision.

It is generally believed that the acuity of the peripheral visual field is too poor to allow accurate object recognition and, that to be identified, most objects need to be brought into foveal vision by using saccadic eye movements. However, most measures of form vision in the periphery have been done at eccentricities below 10 degrees and have used relatively artificial stimuli such as letters, digits and compound Gabor patterns. Little is known about how such data would apply in the case of more naturalistic stimuli. Here humans were required to categorize briefly flashed (28 ms) unmasked photographs of natural scenes (39 degrees high, and 26 degrees across) on the basis of whether or not they contained an animal. The photographs appeared randomly in nine locations across virtually the entire extent of the horizontal visual field. Accuracy was 93.3% for central vision and decreased almost linearly with increasing eccentricity (89.8% at 13 degrees, 76.1% at 44.5 degrees and 71.2% at 57.5 degrees ). Even at the most extreme eccentricity, where the images were centred at 70.5 degrees, subjects scored 60.5% correct. No evidence was found for hemispheric specialization. This level of performance was achieved despite the fact that the position of the image was unpredictable, ruling out the use of precued attention to target locations. The results demonstrate that even high-level visual tasks involving object vision can be performed using the relatively coarse information provided by the peripheral retina.

Adult↗
PubMed2001

Pursuit eye movements to second-order motion targets.

We studied smooth-pursuit eye movements elicited by first- and second-order motion stimuli. Stimuli were random dot fields whose contrast was modulated by a Gaussian window with a space constant of 0.5 degrees. For the first-order stimuli, the random dots simply moved across the screen at the same speed as the window; for the second-order stimuli the window moved across stationary or randomly flickering dots. Additional stimuli which combined first- and second-order motion cues were used to determine the degree and type of interaction found between the two types of motion stimuli. Measurements were made at slow (1 degrees/s) and moderate (6 degrees/s) target speeds. At a velocity of 1 degrees/s the initiation, transition, and steady-state phases of smooth pursuit in response to second-order motion targets are severely affected when compared with the smooth pursuit of first-order motion targets. At a velocity of 6 degrees/s there is a small but significant deficit in steady-state pursuit of second-order motion targets but not much effect on pursuit initiation.

Contrast Sensitivity↗
PubMed2001

Effects of visual illusions on grasping.

In 2 experiments, the Muller-Lyer illusion (F. C. Muller-Lyer, 1889; N = 16) and the parallel-lines illusion (W. Wundt, 1898; N = 26) clearly affected maximum preshape aperture in grasping (both ps < .001). The grasping effects were similar but not perfectly equal to the perceptual effects. Control experiments show that these differences can be attributed to problems in matching the perceptual task and the grasping task. A model is described stating the assumptions that are needed to compare the grasping effects and the perceptual effects of visual illusions. Further studies on the relationship between perception and grasping are reviewed. These studies provide no clear evidence for a dissociation between perception and grasping and therefore do not support the action versus perception hypothesis (A. D. Milner & M. A. Goodale, 1995).

Adolescent↗
PubMed2000

Sensory and cognitive contributions of color to the recognition of natural scenes.

Although color plays a prominent part in our subjective experience of the visual world, the evolutionary advantage of color vision is still unclear [1] [2], with most current answers pointing towards specialized uses, for example to detect ripe fruit amongst foliage [3] [4] [5] [6]. We investigated whether color has a more general role in visual recognition by looking at the contribution of color to the encoding and retrieval processes involved in pattern recognition [7] [8] [9]. Recognition accuracy was higher for color images of natural scenes than for luminance-matched black and white images, and color information contributed to both components of the recognition process. Initially, color leads to an image-coding advantage at the very early stages of sensory processing, most probably by easing the image-segmentation task. Later, color leads to an advantage in retrieval, presumably as the result of an enhanced image representation in memory due to the additional attribute. Our results ascribe color vision a general role in the processing of visual form, starting at the very earliest stages of analysis: color helps us to recognize things faster and to remember them better.

Cognition↗
PubMed2000

Time course of chromatic adaptation for color appearance and discrimination.

Adaptation to a steady background has a profound effect on both color appearance and discrimination. We determined the temporal characteristics of chromatic adaptation for appearance and discrimination along different color directions. Subjects were adapted to a large uniform background made up of a CRT screen and a 45x64 degrees wall, illuminated by computer controlled lamps. After an instant change in background color along a red-green or blue-yellow color axis, we measured thresholds for the detection of increments along the same axes at fixed times between 25 ms and 121 s. Analogously, color appearance was determined using achromatic matching. Three components of adaptation could be identified by their temporal characteristics. A slow exponential time course of adaptation with a half-life of about 20 s was common to appearance and discrimination. A faster component with a half-life of 40-70 ms--probably due to photoreceptor adaptation--was also common to both. Exclusive for color appearance, there was a third, extremely rapid mechanism with a half-life faster than 10 ms. This instantaneous process explained more than 50% of total adaptation for color appearance and could be shown to act in a multiplicative manner. We conclude that this instantaneous adaptation mechanism for color appearance is situated at a later processing stage, after mechanisms common to appearance and discrimination, and is based on multiplicative spatial interactions rather than on local, temporal adaptational processes. Color appearance, and thus color constancy, seems to be determined in large part by cortical computations.

Adaptation, Physiological↗
PubMed2000

The colors seen behind transparent filters.

How do the colors and lightnesses of surfaces seen to lie behind a transparent filter depend on the chromatic properties of the filter? A convergence model developed in prior work (D'Zmura et al, 1997 Perception 26 471-492; Chen and D'Zmura, 1998 Perception 27 595-608) suggests that the visual system interprets a filter's transformation of color in terms of a convergence in color space. Such a convergence is described by a color shift and a change in contrast. We tested the model using an asymmetric matching task. Observers adjusted, in computer graphic simulation, the color of a surface seen behind a transparent filter in order to match the color of a surface seen in plain view. The convergence model fits the color-matching results nearly as well as a more general affine-transformation model, even though the latter has many more parameters. Other models, including von Kries scaling, did not perform as well. These results suggest that the color constancy revealed in this task is described best by a model that takes into account both color shifts and changes in contrast.

Color Perception↗
PubMed2000

Velocity constancy in a virtual reality environment.

During everyday life the brain is continuously integrating multiple perceptual cues in order to allow us to make decisions and to guide our actions. In this study we have used a simulated (virtual reality--VR) visual environment to investigate how cues to speed judgments are integrated. There are two sources that could be used to provide signals for velocity constancy: temporal-frequency or distance cues. However, evidence from most psychophysical studies favours temporal-frequency cues. Here we report that two depth cues that provide a relative object--object distance--disparity and motion parallax--can provide a significant input to velocity-constancy judgments, particularly when combined. This result indicates that the second mechanism can also play a significant role in generating velocity constancy. Furthermore, we show that cognitive factors, such as familiar size, can influence the perception of object speed. The results suggest that both low-level cues to spatiotemporal structure and depth, and high-level cues, such as object familiarity, are integrated by the brain during velocity estimation in real-world viewing.

Cues↗
PubMed2000

Grasping visual illusions: no evidence for a dissociation between perception and action.

Neuropsychological studies prompted the theory that the primate visual system might be organized into two parallel pathways, one for conscious perception and one for guiding action. Supporting evidence in healthy subjects seemed to come from a dissociation in visual illusions: In previous studies, the Ebbinghaus (or Titchener) illusion deceived perceptual judgments of size, but only marginally influenced the size estimates used in grasping. Contrary to those results, the findings from the present study show that there is no difference in the sizes of the perceptual and grasp illusions if the perceptual and grasping tasks are appropriately matched. We show that the differences found previously can be accounted for by a hitherto unknown, nonadditive effect in the illusion. We conclude that the illusion does not provide evidence for the existence of two distinct pathways for perception and action in the visual system.

Consciousness↗
PubMed2000

Motion perception at scotopic light levels.

Although the spatial and temporal properties of rod-mediated vision have been extensively characterized, little is known about scotopic motion perception. To provide such information, we determined thresholds for the detection and identification of the direction of motion of sinusoidal grating patches moving at speeds from 1 to 32 deg/s, under scotopic light levels, in four different types of observers: three normals, a rod monochromat (who lacks all cone vision), an S-cone monochromat (who lacks M- and L-cone vision), and four deuteranopes (who lack M-cone vision). The deuteranopes, whose motion perception does not differ from that of normals, allowed us to measure rod and L-cone thresholds under silent substitution conditions and to compare directly the perceived velocity for moving stimuli detected by either rod or cone vision at the same light level. We find, for rod as for cone vision, that the direction of motion can be reliably identified very near to detection threshold. In contrast, the perceived velocity of rod-mediated stimuli is reduced by approximately 20% relative to cone-mediated stimuli at temporal frequencies below 4 Hz and at all intensity levels investigated (0.92 to -1.12 log cd m(-2)). Most likely, the difference in velocity perception is distal in origin because rod and cone signals converge in the retina and further processing of their combined signals in the visual cortex is presumably identical. To account for the difference, we propose a model of velocity, in which the greater temporal averaging of rod signals in the retina leads to an attenuation of the motion signal in the detectors tuned to high velocities.

Color Vision Defects↗
PubMed1999

Selective color constancy deficits after circumscribed unilateral brain lesions.

The color of an object, when part of a complex scene, is determined not only by its spectral reflectance but also by the colors of all other objects in the scene (von Helmholtz, 1886; Ives, 1912; Land, 1959). By taking global color information into account, the visual system is able to maintain constancy of the color appearance of the object, despite large variations in the light incident on the retina arising from changes in the spectral content of the illuminating light (Hurlbert, 1998; Maloney, 1999). The neural basis of this color constancy is, however, poorly understood. Although there seems to be a prominent role for retinal, cone-specific adaptation mechanisms (von Kries, 1902; Pöppel, 1986; Foster and Nascimento, 1994), the contribution of cortical mechanisms to color constancy is still unclear (Land et al., 1983; D'Zmura and Lennie, 1986). We examined the color perception of 27 patients with defined unilateral lesions mainly located in the parieto-temporo-occipital and fronto-parieto-temporal cortex. With a battery of clinical and specially designed color vision tests we tried to detect and differentiate between possible deficits in central color processing. Our results show that color constancy can be selectively impaired after circumscribed unilateral lesions in parieto-temporal cortex of the left or right hemisphere. Five of 27 patients exhibited significant deficits in a color constancy task, but all of the 5 performed well in color discrimination or higher-level visual tasks, such as the association of colors with familiar objects. These results indicate that the computations underlying color constancy are mediated by specialized cortical circuitry, which is independent of the neural substrate for color discrimination and for assigning colors to objects.

Adaptation, Physiological↗
PubMed1999

Velocity tuned mechanisms in human motion processing.

We determined two-dimensional motion discrimination contours in the spatio-temporal frequency plane to characterize the mechanisms underlying velocity perception. In particular, we wanted to determine whether there exist mechanisms tuned specifically to velocity, rather than separable mechanisms tuned to spatial and temporal frequency. A 4-AFC paradigm was used to determine spatio-temporal frequency discrimination thresholds for moving sinewave gratings defined by luminance contrast. Three of the grating patches used were defined by the same spatial and temporal frequency (standard), the other (test) differed by a fixed proportional change in spatial and temporal frequency. Subjects had to indicate which grating differed most from the others and the thresholds determined for varying proportions of change in spatial and temporal frequency were used to trace out complete threshold contours in the plane spanned by these attributes. Some of the contours, primarily at speeds above 1 deg/s, were noticeably oriented along lines of constant velocity. To further isolate these mechanisms, spatio-temporal noise was added to the standard stimuli either along a line of constant velocity or in the direction orthogonal to it. When spatio-temporal noise of constant velocity was added to the standard stimuli, threshold contours became elongated only along the direction of the noise. The same amount of noise in the orthogonal direction produced an overall increase in thresholds without changing the shape of the contour, presenting clear evidence for velocity tuned mechanisms. In further experiments we discovered that velocity tuned mechanisms interact with separable mechanisms to produce optimal discriminability. Analogous experiments with isoluminant stimuli failed to exhibit evidence for velocity tuning, supporting the notion that the human color vision system is impaired in its coding of stimulus speed, despite excellent sensitivity to direction of motion.

Discrimination, Psychological↗
PubMed1999

Contrast sensitivity and appearance in briefly presented illusory figures.

We examined the contributions of brightness enhancement, illusory figure formation and figural completion to changes in contrast sensitivity in contour gaps. The brightness on the border of a Kanizsa-square and an outline square was measured as the point of subjective equality with the background (PSE) for small line targets. Increment and decrement thresholds were measured at the same location. We found that contrast thresholds were lower than in a control condition without inducers, and that the threshold reduction was independent of the contrast polarity of the inducers. This reduction cannot be explained by a simple summation of stimulus contrast and induced brightness. In a second experiment the inducers that define the contour of the Kanizsa and the outline square were changed so that the figure was no longer closed, keeping the local stimulus surround constant. Thresholds were equally reduced for all conditions, independently of whether the figure was completed or not, or whether an illusory contour was perceived or not. The results suggest that the reduction of contrast threshold in contour gaps is independent of the brightness perceived in these gaps and of the formation of an illusory figure. Processes that cause contrast threshold reduction in contour gaps also seem to operate independently of figural completion.

Adaptation, Ocular↗
PubMed1998

The contribution of color to visual memory in X-chromosome-linked dichromats.

We used a recognition memory paradigm to assess the visual memory of X-chromosome-linked dichromats for color images of natural scenes. The performance of 17 protanopes and 14 deuteranopes, who lack the second (red-green opponent) subsystem of color vision, but retain the primordial (yellow-blue opponent) subsystem, was compared with that of 36 color normal observers. During the presentation phase, 48 images of natural scenes were displayed on a CRT for durations between 50 and 1000 msec. Each image was followed by a random noise mask. Half of the images were presented in color and half in black and white. In the subsequent query phase, the same 48 images were intermixed with 48 new images and the subjects had to indicate which of the images they had already seen during the presentation phase. We find that the performance of the color normal observers increases with exposure duration. However, they perform 5-10% better for colored than for black and white images, even at exposure durations as short as 50 msec. Surprisingly, performance is not impaired for the dichromats, whose recognition performance is also better for colored than for black and white images. We conclude either that X-chromosome-linked dichromats may be able to compensate for their reduced chromatic information range when viewing complex natural scenes or that the chromatic information in most natural scenes, for the durations tested, is sufficiently represented by the surviving primordial color subsystem.

Adult↗
PubMed1998

Thresholds for the identification of the direction of motion of plaid patterns defined by luminance or chromatic contrast.

Contrast thresholds for identification of the direction of motion were determined for sinusoidal gratings and plaid patterns moving in eight possible directions. Since plaid patterns are the sum of two component gratings, a prediction of the thresholds for plaids can be made by assuming that the motions of both component gratings are independently identified (probability summation). In agreement with standard two-stage models of plaid perception, our results show that for stimuli defined by luminance contrast, plaid direction thresholds can be predicted well from the component thresholds. This also holds for fast-moving isoluminant plaid patterns, but for slowly moving (< 4 Hz) isoluminant plaids, direction thresholds were substantially higher than the prediction from the components. In the latter case, subjects frequently were unable to identify the motion of the plaid in the pattern direction, even when the direction of motion of both components could be reliably identified. Different mechanisms might underlie the perception of luminance and isoluminant plaids at slow speeds.

Color Perception↗
PubMed1998

Effects of contrast and temporal frequency on orientation discrimination for luminance and isoluminant stimuli.

We compared the mechanisms responsible for orientation discrimination of stimuli defined by luminance and red/green isoluminant contrast. A four-alternative forced-choice (4-AFC) paradigm was used to determine thresholds for discriminating 1 cpd sinewave gratings differing in orientation, contrast, or both. When measuring orientation thresholds as a function of stimulus contrast, we found a decrease in thresholds with increasing stimulus contrast. For three temporal frequencies (0, 1, and 8 Hz) the functions relating orientation thresholds to stimulus contrast had similar shapes for luminance and isoluminant gratings, indicating similar processing mechanisms. Thresholds for stationary or slowly moving gratings were consistently lower for isoluminant than for luminance gratings, when contrast was expressed on an absolute RMS-cone-contrast scale. When contrast was defined as multiples of detection thresholds, discrimination was slightly better for luminance gratings. Thresholds for fast moving gratings were similar, irrespective of the definition of contrast. In contrast to previous work, we found a marked "oblique-effect" for both luminance and isoluminant gratings, when measuring discrimination thresholds as a function of standard orientation. Finally, we measured discrimination thresholds for gratings that varied in contrast and orientation simultaneously. The shapes of the resulting two-dimensional threshold contours were similar for luminance and isoluminant gratings, indicating again that these stimuli undergo similar neuronal processing. Performance of the observers could be described by probability summation of the orientation and contrast cues, resulting in an elliptical shape of the two-dimensional threshold contours. In conclusion, our results show similar performance for luminance and isoluminant gratings in several orientation discrimination tasks. The similarity in shape of the different threshold functions presents strong evidence that similar mechanisms underlie orientation discrimination of luminance and isoluminant stimuli.

Color Perception↗