THE EFFECT OF SIMULATED AIRCRAFT SPEED ON DETECTING AND IDENTIFYING TARGETS FROM SIDE-LOOKING-RADAR IMAGERY. TECHN DOCUM REP NO. AMRL-TDR-64-40.
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Three experiments investigated 4.5-month-old infants' perception of the unity and boundaries of haptically presented objects. When infants actively explored the two handles of an unseen object assembly, perception of the unity of the assembly depended on the handles' motion. Infants perceived a single, connected object if the handles moved rigidly together, and they perceived two distinct objects if the handles underwent relative vertical or horizontal motion. When infants passively explored the same object assembly undergoing the same motions, object perception appeared to be indeterminate. The findings of the active motion experiments accord with the findings of studies of visual object perception and suggest that object perception depends on amodal processes, operating on representations of either seen or felt surface motions. The findings of the passive motion experiments nevertheless suggest a difference between visual and haptic perception: for infants as for adults, haptic perception is enhanced by the active production of surface motion.
How does the visual system generate percepts of moving forms? How does this happen when the forms are emergent percepts, such as illusory contours or segregated textures, and the motion percept is apparent motion between the emergent forms? We develop a neural model of form-motion interactions to explain and simulate parametric properties of psychophysical motion data and to make predictions about how the parallel cortical processing streams V1-->MT and V1-->V2-->MT control form-motion interactions. The model explains how an illusory contour can move in apparent motion to another illusory contour or to a luminance-derived contour; how illusory contour persistence relates to the upper interstimulus interval (ISI) threshold for apparent motion; and how upper and lower ISI thresholds for seeing apparent motion between two flashes decrease with stimulus duration and narrow with spatial separation (Korte's laws). The model accounts for these data by suggesting how the persistence of a boundary segmentation in the V1-->V2 processing stream influences the quality of apparent motion in the V1-->MT stream through V2-->MT interactions. These data may all be explained by an analysis of how orientationally tuned form perception mechanisms and directionally tuned motion perception mechanisms interact.
Are there visual cells in the cat superior colliculus, selectively sensitive to relative pattern movement? Based on extracellular recordings from paralyzed pretrigeminal preparations, a sample of 76 collicular units could be divided into two main types according to relative movement sensitivity: those that responded optimally and selectively to one specific relative velocity between a small disk and a full-field grating; and those that discharged maximally whenever the grating shifted relative to a disk moving at one specific "absolute" speed, regardless of the precise relative velocity between the two. It was hypothesized that the latter group, in conjunction with extraretinal "calibration" cues, may be part of a neural mechanism encoding spatial depth in terms of motion parallax.
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Following an extensive single subject pilot study 12 Ss viewed a continuously cycling (3 Hz), two stimulus, apparent motion (AM) display. The "AM breakdown effect" was utilised to gather visual evoked potentials (VEPs) from sites O1, O2, T5, T6, P3, and P4 during periods in which the display elicited either: the percept of motion; or the percept of two discrete alternating stimuli. VEPs displayed components of larger amplitude during motion periods in all right (but no left) hemisphere sites during periods 60-82 msec post left field stimulus onset (positive component) and 100-126 msec post right field stimulus onset (negative component). Results were interpreted as indicating initial extraction of motion information within the occipital lobe, with further motion processing taking place in temporal and parietal lobes.
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Participants observed a point-light character (PLC) performing a gymnastic movement. They either memorized the final PLC orientation from the initial viewpoint, to match it to a test posture (memory task), or judged whether the biological motion appeared continuous (perceptual task), despite a viewpoint change. The observer could be either static or virtually in motion (pan or track) while looking at the movement from the initial viewpoint. The presence of a spatial layout during virtual self-motion induced a global optical flow specifying the translational component of the PLC movement, rendering the event more predictable for the participants. A representational momentum effect was observed in the memory task, suggesting that when a visual stimulation, such as a PLC motion, is abruptly stopped, its dynamics survive. In contrast, structural and transformational invariants specifying the PLC motion were sufficient to solve the perceptual task accurately. Finally, both the remembering of the final posture and the perception of continuity degraded with an increase in viewpoint change due to tilt/slant posture orientation matching, indicating that orientation processes interfered with event perception.
For proper manual aircraft control, the pilot has to perceive the motion state of the aircraft. In this perception process both the visual and the vestibular systems play an important role. To understand this perception process and its impact on a pilot's control behavior a descriptive model was developed. The single-channel information-processor model was applied as the basic structure of the final model. Three groups of experiments were performed to refine the model structure and to define the majority of the model parameters. The model has been evaluated by measuring the control behavior in tracking tasks.
Although recent fMRI and single unit recording studies have shown that attention modulates neural activity in motion sensitive areas of extrastriate cortex, these approaches cannot reveal qualitative or quantitative effects of attention on perception of motion. To investigate this, we asked observers to select one of two orthogonal directions in a brief, transparent dot display (prime) and then measured their sensitivity to global directional motion in a second uni-directional dot display (probe) presented a short time later. When probe direction matched the attended prime direction, sensitivity was degraded. But, when probe direction matched the ignored prime direction, sensitivity was enhanced, even though both components were of equal physical strength. Sensitivity was unchanged for directions opposite to either previously seen direction. Neither sensory adaptation nor opponent direction mechanisms can account for these data. Rather, processes initiated by visual selection must underlie these dramatic changes in motion sensitivity.
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The phenomenon of non-Fourier motion (visually perceived motion that cannot be explained simply on the basis of the autocorrelation structure of the visual stimulus) is well recognized, and is generally considered to be due to nonlinear preprocessing of the visual stimulus prior to a stage of standard motion analysis. We devised a sequence of novel visual stimuli in which the availability of a motion stimulus depends on the nature of the nonlinear preprocessing: an nth order stimulus Pn will generate a perception of motion if it is preprocessed by a nonlinearity of polynomial order n or greater, but not if preprocessed by a nonlinearity of polynomial order less than n. We found that unambiguous motion direction was perceived for P2, P3, and P4, but not for higher-order stimuli, and we measured the contrast thresholds for direction discrimination with superimposed noise. We found that an asymmetric compressive nonlinearity can, in a unified fashion, account for these results, while a purely quadratic nonlinearity or a rectification of the form T(p) = magnitude of p cannot. We compared velocity discrimination judgements for second-order non-Fourier stimuli (P2) with standard drifting gratings. Although velocity comparisons were veridical, uncertainties were greater for the non-Fourier stimuli. This could be reproduced by substituting a Fourier grating with superimposed noise for the non-Fourier grating. These findings are consistent with a single pathway which processes both Fourier and non-Fourier short-range motion, and are discussed in the context of other investigations which have been interpreted as demonstrating separate pathways.