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L Spillmann

Publications and source records attributed to L Spillmann.

At least 19 recordsLinked to original sources

Motion and shape in common fate.

We determined how much motion coherence was needed to detect a target group of four moving dots in a dynamic visual noise (DVN) background. The lifetimes of the trajectories of the target and that of the noise dots were the same. In addition to parallel trajectories and collinear dot arrangements, divergent, convergent, or crossing trajectories and non-collinear dot arrangements were also tested. Performance saturated at a lifetime of approximately 600 ms. It was best for parallel trajectories and collinear dots, and worse for crossed trajectories with non-collinear dots, where it approached performance in a no-motion, form-only control experiment. Results illustrate the importance of common fate in motion perception in DVN, when other factors are equated.

Adult↗

The scintillating grid illusion in stereo-depth.

The dark scintillating dots occurring on a gray-on-black, modified Hermann grid [Schrauf, M., Lingelbach, B., & Wist, E. R. (1997). The scintillating grid illusion. Vision Research, 37, 1033-1038] were studied in stereo-depth by assigning various degrees of disparity to the white inducing disks. Dependent on the sign of disparity, the disks and the dark illusory spots within them appeared to lie either in the same plane, in front of, or behind the grid. At zero disparity, illusory strength was maximum and was the same for stereo, binocular and monocular viewing. With increasing disparity, the illusion became progressively weaker; however, the decrease for stereo-patterns was significantly less than for control patterns presented binocularly or monocularly. These results suggest a central contribution to the scintillation effect.

Adult↗

S-cone signals to temporal OFF-channels: asymmetrical connections to postreceptoral chromatic mechanisms.

Psychophysical tests of S-cone contributions to temporal ON- and OFF-channels were conducted. Detection thresholds for S-cone modulation were measured with two kinds of test stimuli presented on a CRT: a rapid-on sawtooth test and a rapid-off sawtooth test, assumed to be detected differentially by temporal ON- and OFF-channels, respectively. S-cone related ON- and OFF-temporal responses were separated by adapting for 5 min to 1 Hz monochromatic (420, 440, 450, 540, or 650 nm in separate sessions) sawtooth flicker presented in Maxwellian view. Circular test stimuli, with a sawtooth temporal profile and a Gaussian spatial taper, were presented for 1 s in one of four quadrants 1.0 degree from a central fixation point. A four-alternative forced-choice method combined with a double-staircase procedure was used to determine ON- and OFF-thresholds in the same session. Following adaptation, the threshold elevation was greater if the polarity of the test stimulus was the same as the polarity of the sawtooth adaptation flicker, consistent with separate ON- and OFF-responses from S-cones. This asymmetrical pattern was obtained, however, only when the adaptation stimuli appeared blue with a little redness. When the adaptation flicker had a clear reddish hue component, the threshold elevation did not depend on the polarity of the sawtooth test stimuli. These results are consistent with a model in which OFF-signals originating from S cones are maintained by a postreceptoral mechanism signaling redness, but not by a postreceptoral chromatic mechanism signaling blueness.

Adaptation, Ocular↗

Spatial distortions in rotating radial figures.

A white sector on a black rotating disk appears spatially compressed. We found that apparent shrinkage: (1) for sectors ranging from 15 to 150 degrees and rotating at 1.25 rps varied in an inverted U-shaped manner from 3 to 16 degrees and back to 11 degrees (corresponding to 20, 16, and 7.5%, respectively); (2) increased with speed of rotation producing maximal compressions of between 7 and 30 degrees for velocities ranging from 0.8 to 2 rps; and (3) affected the leading and the trailing portions of the rotating sector equally, while allowing for apparent expansion of the middle region. Consistent with these findings we found that (4) two black lines 20 mm apart across the center of the rotating disk and extending outward towards the edge appeared to converge when they were actually parallel and were seen as parallel when their end points were physically diverged by 6 degrees. Our findings suggest a foreshortening process which ensures that the shapes of moving stimuli are perceived approximately correctly, irrespective of whether they are actually sharp or blurred.

Adult↗

From elements to perception: local and global processing in visual neurons.

Gestalt psychologists in the early part of the century challenged psychophysical notions that perceptual phenomena can be understood from a punctate (atomistic) analysis of the elements present in the stimulus. Their ideas slowed later attempts to explain vision in terms of single-cell recordings from individual neurons. A rapprochement between Gestalt phenomenology and neurophysiology seemed unlikely when the first ECVP was held in Marburg, Germany, in 1978. Since that time, response properties of neurons have been discovered that invite an interpretation of visual phenomena (including illusions) in terms of neuronal processing by long-range interactions, as first proposed by Mach and Hering in the last century. This article traces a personal journey into the early days of neurophysiological vision research to illustrate the progress that has taken place from the first attempts to correlate single-cell responses with visual perceptions. Whereas initially the receptive-field properties of individual classes of cells--e.g., contrast, wavelength, orientation, motion, disparity, and spatial-frequency detectors--were used to account for relatively simple visual phenomena, nowadays complex perceptions are interpreted in terms of long-range interactions, involving many neurons. This change in paradigm from local to global processing was made possible by recent findings, in the cortex, on horizontal interactions and backward propagation (feedback loops) in addition to classical feedforward processing. These mechanisms are exemplified by studies of the tilt effect and tilt aftereffect, direction-specific motion adaptation, illusory contours, filling-in and fading, figure--ground segregation by orientation and motion contrast, and pop-out in dynamic visual-noise patterns. Major questions for future research and a discussion of their epistemological implications conclude the article.

Contrast Sensitivity↗

Reversed visual motion and self-sustaining eye oscillations.

A random-dot field undergoing counterphase flicker paradoxically appears to move in the same direction as head and eye movements, i.e. opposite to the optic-flow field. The effect is robust and occurs over a wide range of flicker rates and pixel sizes. The phenomenon can be explained by reversed phi motion caused by apparent pixel movement between successive retinal images. The reversed motion provides a positive feedback control of the display, whereas under normal conditions retinal signals provide a negative feedback. This altered polarity invokes self-sustaining eye movements akin to involuntary optokinetic nystagmus.

Eye Movements↗

Colour in a larger perspective: the rebirth of Gestalt psychology.

This overview takes the reader from the classical contrast and assimilation studies of the past to today's colour research, in a broad sense, with its renewed emphasis on the phenomenological qualities of visual perception. It shows how the shift in paradigm from local to global effects in single-unit recordings prompted a reappraisal of appearance in visual experiments, not just in colour, but in the perception of motion, texture, and depth as well. Gestalt ideas placed in the context of modern concepts are shown to inspire psychophysicists, neurophysiologists, and computational vision scientists alike. Feedforward, horizontal interactions, and feedback are discussed as potential neuronal mechanisms to account for phenomena such as uniform surfaces, filling-in, and grouping arising from processes beyond the classical receptive field. A look forward towards future developments in the field of figure-ground segregation (Gestalt formation) concludes the article.

Color Perception↗

Brightness fading during Ganzfeld adaptation.

The time course and extent of brightness fading in a Ganzfeld were determined for adapting luminances ranging from 0.01 to 100 cd/m2. Magnitude estimation and interocular brightness matching were used. During Ganzfeld adaptation, perceived brightness decreased slowly and leveled off, on average, after 5-7 min (adapting time increasing with luminance). On average, the total brightness loss was equivalent to a 1.2 log unit reduction in luminance, independent of adapting luminance. The residual brightness perceived at the final plateau was generally higher than the brightness of the Eigengrau, suggesting a partially sustained luminance channel.

Adaptation, Physiological↗

The abutting grating illusion.

Two line gratings abutting each other with a phase shift of half a cycle elicit the perception of an illusory line running orthogonally between the two sets of grating lines. We found that rating strength increases with increasing number of lines, line length, and phase angle. In contrast, rating strength decreases with increasing spacing of lines, lateral misalignment, rotation of one grating relative to the other, and line width. There is a pronounced oblique effect at 45 deg when the orientation of the abutting gratings is changed from horizontal through diagonal to vertical. Findings are interpreted in terms of a neurophysiological model. We conclude that the end-stopped receptive fields activated by the grating lines are about 6 deg long and 2 deg wide. On the other hand, the "response fields" of the cells, integrating orthogonally across line ends, are assumed to be 5 deg long and less than 1 deg wide. The psychophysical data compare favorably with available neurophysiological data in Area V2 of the macaque suggesting that the perception of illusory contours in human observers may be based on cortical cell properties similar to those found in the monkey.

Animals↗

Visual motion aftereffects: critical adaptation and test conditions.

The visual motion aftereffect (MAE) typically occurs when stationary contours are presented to a retinal region that has previously been exposed to motion. It can also be generated following observation of a stationary grating when two gratings (above and below it) move laterally: the surrounding gratings induce motion in the opposite direction in the central one. Following adaptation, the centre appears to move in the direction opposite to the previously induced motion, but little or no MAE is visible in the surround gratings [Swanston & Wade (1992) Perception, 21, 569-582]. The stimulus conditions that generate the MAE from induced motion were examined in five experiments. It was found that: the central MAE occurs when tested with stationary centre and surround gratings following adaptation to surround motion alone (Expt 1); no MAEs in either the centre or surround can be measured when the test stimulus is the centre alone or the surround alone (Expt 2); the maximum MAE in the central grating occurs when the same surround region is adapted and tested (Expt 3); the duration of the MAE is dependent upon the spatial frequency of the surround but not the centre (Expt 4); MAEs can be observed in the surround gratings when they are themselves surrounded by stationary gratings during test (Expt 5). It is concluded that the linear MAE occurs as a consequence of adapting restricted retinal regions to motion but it can only be expressed when nonadapted regions are also tested.

Adaptation, Ocular↗

Long-range interactions in visual perception.

Classical receptive-field concepts have been used to explain local perceptual effects such as border contrast and Mach bands, but are not sufficient to explain global perceptual effects. Examples are the perception of illusory contours, area contrast, color constancy, depth planes, coherent motion and texture contrast. These diverse effects require neurophysiological mechanisms within the visual pathways with long-range interactions. Candidate mechanisms are suggested, including converging feedforward projection to account for the emergence of new response properties at higher levels, recruitment of lateral connections to compensate for loss of afference and explain filling-in, and re-entrant projections from higher levels using synchronization of neuronal responses to account for binding.

Animals↗

Assimilation: asymmetry between brightness and darkness?

A pincushion formed by four arcs on a gray background looks darker when the arcs are black, and lighter when the arcs are white. Yet, a matching-experiment shows that this difference is relative. Whereas the apparently darker pincushion requires a matching luminance that is lower than the background luminance (i.e. assimilation), the apparently lighter pincushion curiously is also matched to a darker-than-background value (i.e. simultaneous contrast). A change-over in direction of a higher luminance occurs only at the lowest contrast. The size of the decrement required for matching the brightness of the pincushions increases with increasing contrast of the inducing stimulus, as well as with viewing distance. Assimilation is found also in the domain of color, however, only when the luminance of the colored inducers is below that of the background. Analogous asymmetries in the perception of darkness and lightness are discussed.

Color Perception↗

Phenomena of illusory form: can we bridge the gap between levels of explanation?

The study of illusory brightness and contour phenomena has become an important tool in modern brain research. Gestalt, cognitive, neural, and computational approaches are reviewed and their explanatory powers are discussed in the light of empirical data. Two well-known phenomena of illusory form are dealt with, the Ehrenstein illusion and the Kanizsa triangle. It is argued that the gap between the different levels of explanation, bottom-up versus top-down, creates scientific barriers which have all too often engendered unnecessary debate about who is right and who is wrong. In this review of the literature we favour an integrative approach to the question of how illusory form is derived from stimulus configuration which provide the visual system with seemingly incomplete information. The processes that can explain the emergence of these phenomena range from local feature detection to global strategies of perceptual organisation. These processes may be similar to those that help us restore partially occluded objects in everyday vision. To understand better the Ehrenstein and Kanizsa illusions, it is proposed that different levels of analysis and explanation are not mutually exclusive, but complementary. Theories of illusory contour and form perception must, therefore, take into account the underlying neurophysiological mechanisms and their possible interactions with cognitive and attentional processes.

Arousal↗

The Hermann grid illusion: a tool for studying human perspective field organization.

Psychophysical research on the Hermann grid illusion is reviewed and possible neurophysiological mechanisms are discussed. The illusion is most plausibly explained by lateral inhibition within the concentric receptive fields of retinal and/or geniculate ganglion cells, with contributions by the binocular orientation-specific cortical cells. Results may be summarized as follows: (a) For a strong Hermann grid illusion to be seen bar width must be matched to the mean size of receptive-field centers at any given retinal eccentricity. (b) With the use of this rationale, the diameter of foveal perceptive-field centers (the psychophysical correlate of receptive-field centers) has been found to be in the order of 4-5 min arc and that of total fields (centers plus surrounds) 18 min arc. These small diameters explain why the illusion tends to be absent in foveal vision. (c) With increasing distance from the fovea, perceptive-field centers increase to 1.7 deg at 15 deg eccentricity and then to 3.4 deg at 60 deg eccentricity. This doubling in diameter agrees with the change in size of retinal receptive-field centers in the monkey. (d) The Hermann grid illusion is diminished with dark adaptation. This finding is consistent with the reduction of the center-surround antagonism in retinal receptive fields. (e) The illusion is also weakened when the grid is presented diagonally, which suggests a contribution by the orientation-sensitive cells in the lateral geniculate nucleus and visual cortex. (f) Strong induction effects, similar to the bright and dark spots in the Hermann grid illusion, may be elicited by grids made of various shades of grey; and by grids varying only in chroma or hue. Not accounted for are: the illusory spots occurring in an outline grid ie with hollow squares, and the absence of an illusion when extra bars are added to the grid. Alternative explanations are discussed for the spurious lines connecting the illusory spots along the diagonals and the fuzzy dark bands traversing the rhombi in modified Hermann grids.

Animals↗

The perception of movement and depth in moiré patterns.

Moiré patterns can produce striking movement effects and in more complex stimuli can induce vivid stereoscopic depth. The physical rules underlying these phenomena are reviewed and their relationship to psychophysics is discussed. First, it is shown how moirés in 'optical line interference' patterns are created by superimposing periodic visual stimuli, eg gratings, and shifting them relative to each other. When two gratings are presented in this manner, small differences in spatial frequency, orientation, and speed are magnified. This magnification has prompted the use of moiré patterns both in industry and in art where their enhanced sensitivity to misalignment and spatial distortion has been widely exploited. Next, it is demonstrated how enhanced depth in 'stereoscopic interference' patterns is produced by presenting grating stimuli in two (or more) depth planes. The perceived depth effect in the resulting moiré pattern can be elicited similarly by binocular disparity and motion parallax. Finally, it is described how perceived movements occurring in different directions and at different depths are the basis for the perceptual 'irritations' that fascinate observers in complex moiré patterns. The use of moirés for the noninvasive examination of the human retina by aliasing is discussed.

Contrast Sensitivity↗

Dynamic noise backgrounds facilitate target fading.

With strict fixation, a small uniform target of medium contrast, placed at 10 deg eccentricity, faded much faster when presented on a dynamic random noise background than on either a static random noise background or a uniform background of the same luminance. Time to first disappearance was between 10 and 16 sec when the background was dynamic, 26 sec when it was static, and 57 sec when it was uniform. Times were shortest for temporal noise frequencies of the background between 3.5 and 15 Hz. These findings are unexpected: the frequent change of pixel contrast at the edge of the target should perceptually enhance the border, make it less susceptible to local adaptation, and prevent fading. Instead, dynamic random noise facilitates, rather than suppresses fading. Three potential mechanisms are discussed: edge perturbation, jerk effect and surround induction.

Adaptation, Ocular↗

Reduced spatial sensitization on nonuniform backgrounds.

Spatial sensitivity (Westheimer) functions, when measured on nonuniform backgrounds made up of light dots of 12 min arc, were found to differ in shape, depending on the polarity of the central area on which the test spot was placed. When thresholds were measured on the dark centre between light dots, ie on the adapting-field illumination, the resulting curve was similar to the control curve, measured on a uniform background equated for flux. In comparison, thresholds measured on a central light dot, serving as a pedestal, peaked at larger background diameters and showed much less sensitization compared to the control function.

Adaptation, Ocular↗