Orientational anisotropy in the human visual system

When a target stimulus in a predesignated location is identified by a keypress response, responses are slightly faster if noise stimuli in adjacent locations are identical to the target than if they are a different stimulus assigned to the same response (a repeated-stimulus superiority effect). An exception to this result has been found in experiments that used randomly intermixed letter and digit stimuli. These experiments showed slower responding for identical noise than for nonidentical, response-compatible noise (a repeated-stimulus inferiority effect). The present study investigated these phenomena in three experiments. Experiments 1 and 2 established that both the superiority and inferiority effects can be obtained in the same experiment. They also provided evidence that the repeated-stimulus inferiority effect is a function of the intermixing of letters and digits and not of the larger target-set size that has been used for mixed lists. Experiment 3 demonstrated that, with unmixed presentation, the repeated-stimulus superiority effect is enhanced by an increase in the number of stimuli assigned to each response. The experiments are consistent with accounts that attribute the repeated-stimulus superiority effect to competition that occurs when different internal recognition responses are activated. Moreover, the experiments suggest that the repeated-stimulus inferiority effect has its basis in processes that occur subsequent to feature extraction.     

Horizontal-vertical anisotropy in visual space

We investigated the structure of visual space with a 3D exocentric pointing task. Observers had to direct a pointer towards a ball. Positions of both objects were varied. We measured the deviations from veridical pointing-directions in the horizontal and vertical planes (slant and tilt resp.). The slant increased linearly with an increasing horizontal visual angle. We also examined the effect of relative distance, i.e., the ratio of the distances between the two objects and the observer. When the pointer was further away from the observer than the ball, the observer directed the pointer in between himself and the ball, whereas when the pointer was closer to the observer he directed the pointer too far away. Neither the horizontal visual angle nor the relative distance had an effect on the tilt. The vertical visual angle had no effect on the deviations of the slant, but had a linear effect on the tilt. These results quantify the anisotropy of visual space.     

Spatiotemporal isosensitivity fields in the human visual system

The human visual system is capable of detecting correlations, manifested perceptually as global pattern, in mathematically constrained dynamic textures. This ability has given rise to speculation that correlative mechanisms in the human visual system exist and that they have a neural basis similar to the orientationally selective structures discovered in area 17 of the mammalian visual cortex. The limits to the detection of correlation were mapped, spatially and temporally, by means of a psychophysical technique. Evidence is presented that, at least in the spatial domain, the correlation mechanism may be served by a population of such neural units.     

Frequency specific chromatic adaptation in the human visual system

Subjects were exposed to a vertical chromatic grating alternating with horizontal chromatic grating of the identical frequency. They were then tested with a series of test gratings of varied spatial frequencies to examine whether the responses were effected by the spatial frequency of the adaptation pattern in relation to the test pattern. It was found that maximum response occurred when adaptation and test gratings had the same spatial frequency, the effect was asymmetric and finally that enhancements were found at octaves. Thus the experiment further demonstrated that neural elements specific to spatial frequency exist in the human visual system.     

Two channels for flicker in the human visual system

The human visual system contains a large number of narrowly-tuned spatial-frequency-specific channels. Does it contain an analogous set of channels tuned to a narrow range of temporal frequency? On the basis of data gathered with the use of a threshold elevation technique it is argued that human sensitivity to flicker can be accounted for by assuming the existence of just two filters, one a low-pass filter peaking gently at around 6 Hz and one a band-pass filter peaking at around 9 Hz. Similar data gathered from studies of interocular transfer suggest that at least some of the mechanisms involved are binocular, rather than being purely monocular as has previously been suggested.     

Representational content and computation in the human visual system

Summary Information-processing systems can be characterized by their ability to transform systematically certain internal representational states (symbols) into one another. The presence of such an information-processing capacity calls for an explanation. How could such an explanation in principle be formulated? How is it possible to specify internal representational states and to ascribe to them certain representational contents? What has to be demonstrated by such explanations is how an information-processing capacity is actually instantiated in a system. In this paper, the outlines of an explanation by instantiation are sketched for a specific human visual capacity. In addition, some fundamental problems facing the development of this explanation will be discussed.     

Differential luminance sensitivity of the human visual system

In this paper the differential sensitivity of the visual system is investigated by means of two simultaneously presented stimuli in a yes-no procedure. The sensitivity measure σ_I appears to be proportional to stimulus intensity (i.e., Weber’s law). The curve displaying Weber’s law is little affected by variation of the background intensity or of the adaptation level. An increment threshold experiment using only one stimulus yields a proportionality of σ_I with the square root of the background intensity. An additional experiment shows that the sensitivity measure σ_I for two flashes decreases first, from dark up to a particular background intensity, and increases when the background tends to mask the flashes. So, in general, two background levels exist with the same differential sensitivity. The results cannot easily be explained by the simple quantum fluctuation concept. A model based partially on electrophysiological data from the literature is proposed which encounters a particular adaptation mechanism, a transducer with a limited dynamical range, and a range setting mechanism.     

The shape of inhibitory fields in the human visual system

Five point sources of light were displayed sequentially in a horizontal line, with .45 in. of separation between each point, employing a computer-based cathode-ray tube display system. If a particular display order and appropriate display rate is employed, then the first two points being displayed will not be perceived. By systematically varying the spatial location of these two blanked points relative to the three unblanked points, a start is made towards mapping the shape of visual inhibitory fields in man, and this general technique is related to the work of Hartline and of Ratliff on lateral inhibition and to that of Hubel and Wiesel with receptive fields in the cat and monkey striate cortex.     

A forced-choice study of edge detectors in the human visual system

Psychophysical studies using masking procedures to investigate the possible existence of edge detectors in the human visual system have typically been flawed by methodological errors and omissions that make their findings uninterpretable. An example of such a study is given and evaluated, and a replication of that study, using a spatial forced-choice methodology, is reported in detail. The results of this replication are shown to contradict the critical findings of the earlier study; furthermore, it is suggested that any ambiguities in the results of this replication can be interpreted in terms of methodological and procedural factors, rather than in terms of higher-order neurological constructs. Finally, a further test of this methodological interpretation is proposed.     

An examination of a temporal anisotropy in the visual integration of spatial frequencies

Three pairs of experiments were conducted to investigate the importance of spatial-frequency-processing delays imposed by the visual system on the efficacy of their subsequent integration. In the first pair of experiments filtered versions of a natural image were found to be easily discriminable from the full-bandwidth image. These images were then placed into triplets and presented sequentially. Subjects were required to detect the presence of a full-bandwidth target image within the sequence. As with previous results a low-to-high progression of spatial-frequency information did increase the number of errors of full-bandwidth-image detection within the triplets where it was not present. However, this was not found across all conditions and was suggested to be due to the increased discriminability of the constituent images which form the image triplets. The second experiment was a repetition of the first with more confusable component images. Again the weak order effect on target detection was found. It was suggested that this may be due to the nature of the stimulus used. The third pair of experiments repeated the design of the first pair of experiments but with Gabor patches which provide localised spatial-frequency information. It was found that a low-to-high progression of spatial frequencies resulted in more false detections of the target. The results are interpreted as supporting an integration mechanism which operates with greater efficacy when the presentation of spatial-frequency information mirrors that naturally imposed by the neural delays involved in the processing of spatial frequencies.     

Inhibitory interaction between channels sensitive to direction and velocity in the human visual system

Two paradigms for the study of velocity contrast have been employed. Paradigm one has focused on perceived velocity changes across a field. Paradigm two has focused on perceived velocity changes at the juncture of disparate velocities. The current experiments employ both paradigms to look at oppositely directed motion. Using paradigm two, it was determined that, with oppositely directed motion, the effect on perceived velocity could not be attributed to lateral inhibitory interaction--in contrast to earlier reports of lateral interaction when motion was in the same direction. Using paradigm one, it was determined that the effect upon perceived velocity with oppositely directed motion appeared to involve inhibition across entire fields of motion.     

Inhibition between channels selective to contour orientation and wavelength in the human visual system

Recent studies have demonstrated inhibition between channels selective to contour orientation in the human visual system. On the basis of adaptation studies, it has also been suggested that the human visual system contains channels jointly responsive to both contour orientation and wavelength. The present paper investigates inhibition between such channels. Two experiments demonstrated that, with simultaneous presentation of a center vertical target grating and a concentric surround grating, the threshold and the apparent orientation of the center grating depended on the relative orientations of the two gratings and also on whether they were viewed in the same or in different colored light. Color selectivity in both experiments was found across a wider range of angular separations than has generally been reported for successive presentation of the two stimuli. These results suggest inhibition between channels selective to combinations of contour orientation and wavelength in the human visual system.     

Stabilized images: Functional relationships among populations of orientation-specific mechanisms in the human visual system

Two experiments are presented in which fading rates of stabilized line stimuli were measured following prolonged adaptation to nonstabilized grating patterns in various orientations. Results indicated that some orientation-specific effects are sensitive to small variations of orientation around an optimal orientation, as well as to stimuli rotated 90 deg from the optimal orientation. These data were interpreted in terms of interactions among populations of orientation-specific mechanisms in the human visual system.