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Visual sensitivity to stimuli with sinusoidal movement was examined under a number of conditions of binocular stimulation. Sensitivity to stereoscopic movement in depth was reduced in comparison to that for monocular movement. The reduced sensitivity appeared to be due to the presence of stereoscopic depth movement, as opposed to stereoscopic stimulation, binocular movement, or fusion of the images.
About 10 percent of the cells in the visual cortex of awake cats do not respond to stationary parallel stripes in any orientation or to stripes moving across the visual field in any direction at a moderate speed (up to 132 degrees per second), but these cells are either excited or inhibited during saccadic eye movements when the animal faces a patterned visual environment. Of nineteen such cells tested in total darkness, seven discharged in association with eye movements. For saccade-related discharges, the latency during retinal stimulation is typically shorter than the latencey in total darkness.
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Anatomical and physiological observations in monkeys indicate that the primate visual system consists of several separate and independent subdivisions that analyze different aspects of the same retinal image: cells in cortical visual areas 1 and 2 and higher visual areas are segregated into three interdigitating subdivisions that differ in their selectivity for color, stereopsis, movement, and orientation. The pathways selective for form and color seem to be derived mainly from the parvocellular geniculate subdivisions, the depth- and movement-selective components from the magnocellular. At lower levels, in the retina and in the geniculate, cells in these two subdivisions differ in their color selectivity, contrast sensitivity, temporal properties, and spatial resolution. These major differences in the properties of cells at lower levels in each of the subdivisions led to the prediction that different visual functions, such as color, depth, movement, and form perception, should exhibit corresponding differences. Human perceptual experiments are remarkably consistent with these predictions. Moreover, perceptual experiments can be designed to ask which subdivisions of the system are responsible for particular visual abilities, such as figure/ground discrimination or perception of depth from perspective or relative movement--functions that might be difficult to deduce from single-cell response properties.
BACKGROUND: Amblyopia results in deficits in a number of visual functions in both the amblyopic and dominant eye. The present work describes oscillatory movement displacement thresholds (OMDT) in childhood amblyopia. METHODS: The OMDT from the dominant and amblyopic eyes of 50 orthoptic patients (aged 74 (SD 16) months) were compared with those from a group of 24 controls (79 (21) months). OMDT were measured using a forced choice staircase procedure. Subjects were asked to identify which of the computer controlled monitors displayed the oscillating stimulus. Visual acuity and stereoscopic responses were noted from clinical records. RESULTS: Amblyopic children demonstrating stereopsis showed no significant OMDT deficit in the amblyopic eye. Those children having no stereopsis had elevated OMDT in the amblyopic eye (p < 0.05). Results suggest that the dominant eye of children with amblyopia may also have a pattern of visual development which is anomalous (difference in correlation coefficient with age; p < 0.05). CONCLUSION: OMDT deficits demonstrated in some amblyopic eyes indicate that amblyopia is incompletely described by its "clinical" definition. Results suggest that the dominant eye in those with unilateral amblyopia may not be "normal".
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Response properties of single neurons in the middle temporal visual area (MT) of anesthetized owl monkeys were determined and quantified for flashed and moving bars of light under computer control for position, orientation, direction of movement, and speed. Receptive-field sizes, ranging from 4 to 25 degrees in width, were considerably larger than receptive fields with corresponding eccentricities in the striate cortex. Neurons were highly binocular with most cells equally or nearly equally activated by either eye. Neurons varied in selectivity for axis and direction of moving bars. Some neurons demonstrated little or no selectivity, others were bidirectional on a single axis, while the largest group was highly selective for direction with little or no response to bar movement opposite to the preferred direction. Over 70% of neurons were classified as highly selective and 90% showed some preference for direction and/or axis of stimulus movement. Neurons typically responded to bar movement only over a restricted range of velocities. The majority of neurons responded best to a particular velocity within the 5-60 degrees/s range, with marked attenuation of the response for velocities greater or less than the preferred. Some neurons failed to show significant response attenuation even at the lowest tested velocity, while other neurons preferred velocities of 100 degrees/s or more and failed to attenuate to the highest velocities. Response magnitude varied with stimulus dimensions. Increasing the length of the moving bar typically increased the magnitude of the response slightly until the stimulus exceeded the receptive-field borders. Other neurons responded less to increases in bar length within the excitatory receptive field. Neurons preferred narrow bars less than 1 degree in width, and marked reductions in responses characteristically occurred with wider stimuli. Moving patterns of randomly placed small dots were often as effective as or more effective than single bars in activating neurons. Selectivity for direction of movement remained for the dot pattern. for the dot pattern. Poststimulus time (PST) histograms of responses to bars flashed at a series of 21 different positions across the receptive field, in the "response-plane" format, indicated a spatially and temporally homogeneous receptive-field structure for nearly all neurons. Cells characteristically showed transient excitation at both stimulus onset and offset for all effective stimulus locations. Some cells responded mainly at bright stimulus onset or offset.
Tethered, adult female Sphodromantis lineola (Burr.) were presented with two groups of two-dimensional stimuli (i.e., 2-D lures) against various backgrounds. Lure Group 1 comprised various black rectangles in three different size arrays: each size array included a 2, 6, or 12 mm square, respectively, several 'worm' lures of a constant width (l2, edge perpendicular to the direction of movement, 3-30 mm), but varying in length (l1, parallel to the direction of movement, 6-114 mm), and several 'antiworm' lures of a constant length but varying width. Group 1 lures were presented against patterned backgrounds of similar luminance: one natural pattern mimicking foliage and the other a random geometric pattern of rectangles. Group 2 lures comprised various configurations and combinations of black and white lures which were presented against white, black, and natural pattern backgrounds. The appetitive behaviors of approaching and striking at a lure were dependent measures indicating that a stimulus was categorized as prey. For Group 1 lures, overall response rates to lures of the same size were enhanced by the natural pattern background rather than the geometric pattern background. Against the natural pattern background, worm lures were stronger releasers of predatory behavior than antiworm lures of the same size. Lure configuration (especially for the smallest array) was masked by the geometric pattern background, although worm versus antiworm discrimination was apparent with the largest size array. For Group 2 lures, lure-to-background contrast, as well as configuration, effected prey recognition. For instance, lures with low lure-to-background contrast ratios were weaker releasers than those with high ratios, and lures that were darker (versus lighter) than the background were stronger releasers. In addition, particular stimulus properties interacted to effect lure strength. For instance, a weak or strong releaser became stronger or weaker, respectively, when a more or less, respectively, preferred releaser was super-imposed. The results also suggest that S. lineola attends preferentially to the leading edge of a moving stimulus. These findings are in agreement with predatory behavior of praying mantises in the wild.
The visually released, predatory behaviors of approaching and striking at prey by the praying mantis, Sphodromantis lineola (Burr.), were measured in response to various moving, three-dimensional lure configurations. Lures varied in length (3, 7, 15, 25, 35, 50, 70 or 100 mm), thickness (i.e. width and height: 3, 7, 10, 15, 20 or 30 mm) and direction (approaching or moving orthogonally). Each of these three parameters has a significant effect on whether adult female S. lineola recognize a moving object as potential prey. Approaching lures are strong releasers of predatory behaviors when they are 3-35 mm long and 10 mm thick. Orthogonally moving lures, although overall poor releasers of predatory behavior, are at their strongest when 3-35 mm long but only 3 mm thick. These response patterns are similar to those for some anurans and urodeles, which also hunt small invertebrates with analogous behavioral repertoires. This suggests that these groups may have evolved similar algorithms for identifying prey in spite of dissimilar neural organization.
In order to compare visual pattern discrimination by tectal neurons in distantly related vertebrate groups, collicular cells of mice were examined for their responses to each of three simple configurational stimuli commonly used in studies of amphibians. The stimuli consisted of a large square, a horizontal bar and a vertical bar moved at various velocities. Of the recorded units (n = 51), 30-50% significantly preferred the square to the other stimuli at medium (10 degrees/s) and high (67 degrees/s) velocities. Approximately 10% preferred the horizontal bar at these velocities. A significant discrimination between the horizontal and the vertical bar was found in 39% of the units at a velocity of 10 degrees/s, and in 61% at a velocity of 67 degrees/s. These response types are very similar to those found in amphibians; therefore, it is concluded that tectal configurational sensitivity may be a plesiomorphic tetrapod character resulting from basic properties of tectal neuronal circuitry.
A moving grating oriented +/- 45 degrees to the vertical can be perceived at choice as drifting along a left-right or up-down directional axis. When the drifting stimulus is presented alone, direction discrimination thresholds are independent of the specified response-axis. However, they strongly depend on it when the moving stimulus is superimposed on a vertical or horizontal stationary grating. Facilitation is always obtained when the drift direction of the intersections of the two gratings ('blobs') is collinear with the response-axis (i.e. when the orientations of the stationary grating and of the response-axis coincide), while inhibition is observed in the 'noncollinear' cases (i.e. when the orientations of the stationary grating and of the response-axis are orthogonal). These results are generalized in a series of reaction time (RT) experiments where the stimulus configuration described above was set at suprathreshold contrasts and where the orientation/direction of the drifting grating was variable. RT increased when the angle between the response-axis and the direction of the drifting grating increased (uncertainty effect), whether the test stimulus was presented alone, or superimposed on the stationary grating. The uncertainty effect was, however, significantly decreased under 'collinearity' conditions. The attenuation of the uncertainty effect was proportional with the velocity of the blobs and about equal in amount to the RT decrease obtained through the manipulation of the velocity of the drifting grating when presented alone (velocity effect). This observation strongly suggests that both component- and blob/plaid-related information contribute to the directional perception of a compound stimulus and that they sum algebraically.
Sensorimotor adaptation can be defined as a perceptual adaptation whose effects depend on the occurrence and nature of the performed motor actions. Examples of sensorimotor adaptation can be found in the literature on prisms concerning several space-related attributes like orientation, curvature, and size. In this article, we show that sensorimotor adaptation can be obtained for color, as a consequence of the introduction of a new sensorimotor contingency between eye movements and color changes. In an adaptation phase, trials involved the successive presentation of two patches, first on the left, and then on the right or the opposite. The left patch being always red and the right patch green, a correlation is introduced between left-right (respectively right-left) eye saccades and red-green (respectively green-red) color change. After 40 min of adaptation, when two yellow patches are successively presented on each side of the screen, the chromaticity of the left and right patches need respectively to be shifted toward the chromaticity of the red and green adaptation patches for subjective equality to be obtained. When the eyes are kept fixed during the adaptation stage, creating a strong nonhomogeneity in retinal adaptation, no effect is found. This ensures that, if present, adaptation at a given retinal location cannot explain the present effect. A third experiment shows a dependency of the effect on the eyes' saccadic movements and not on the position on the screen, that is, on the position of the eyes in the orbits. These results argue for the involvement of sensorimotor mechanisms in color perception. The relation of these experimental findings toward a sensorimotor theory of color perception is discussed.
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A variety of cell types exist in the temporal cortex providing high-level visual descriptions of bodies and their movements. We have investigated the sensitivity of such cells to different viewing conditions to determine the frame(s) of reference utilized in processing. The responses of the majority of cells in the upper bank of the superior temporal sulcus (areas TPO and PGa) found to be sensitive to static and dynamic information about the body were selective for one perspective view (e.g. right profile, reaching right or walking left). These cells can be considered to provide viewer-centred descriptions because they depend on the observer's vantage point. Viewer-centred descriptions could be used in guiding behaviour. They could also be used as an intermediate step for establishing view-independent responses of other cell types which responded to many or all perspective views selectively of the same object (e.g. head) or movement. These cells have the properties of object-centred descriptions, where the object viewed provides the frame of reference for describing the disposition of object parts and movements (e.g. head on top of shoulders, reaching across the body, walking forward 'following the nose'). For some cells in the lower bank of the superior temporal sulcus (area TEa) the responses to body movements were related to the object or goal of the movements (e.g. reaching for or walking towards a specific place). This goal-centred sensitivity to interaction allowed the cells to be selectively activated in situations where human subjects would attribute causal and intentional relationships.
Equiluminous red-green sine-wave gratings were drifted at a uniform rate in the bottom half of a 10-deg field. In the top half of the display was a sinusoidal-luminance grating of the same spatial frequency and 95% contrast that drifted in the opposite direction. Observers, while fixating a point in the display center, adjusted the speed of this upper comparison grating so that it appeared to match the velocity of the chromatic grating below. At low spatial frequencies, equiluminous gratings were appreciably slowed and sometimes stopped even though the individual bars of the grating could be easily resolved. The amount of slowing was proportionally greatest for gratings with slow drift rates. Blue-yellow sine-wave gratings showed similar effects. When luminance contrast was held constant, increasing chrominance modulation caused further decreases in apparent velocity, ruling out the possibility that the slowing was simply due to decreased luminance contrast. Perceived velocity appears to be a weighted average of luminance and chrominance velocity information.