The relationship of heterophoria to depth perception in aviation. With particular reference to the work of the Royal Canadian Air Force.
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Preparation for extended travel by astronauts within the Solar System, including a possible manned mission to Mars, requires more complete understanding of adaptation to altered inertial environments. Improved understanding is needed to support development and evaluation of interventions to facilitate adaptations during transitions between those environments. Travel to another planet escalates the adaptive challenge because astronauts will experience prolonged exposure to microgravity before encountering a novel gravitational environment. This challenge would have to be met without ground support at the landing site. Evaluation of current adaptive status as well as intervention efficacy can be performed using perceptual, eye movement and postural measures. Due to discrepancies of adaptation magnitude and time-course among these measures, complete understanding of adaptation processes, as well as intervention evaluation, requires examination of all three. Previous research and theory that provide models for comprehending adaptation to altered inertial environments are briefly examined. Reports from astronauts of selected pre- in- and postflight self-motion illusions are described. The currently controversial tilt-translation reinterpretation hypothesis is reviewed and possible resolutions to the controversy are proposed. Finally, based on apparent gaps in our current knowledge, further research is proposed to achieve a more complete understanding of adaptation as well as to develop effective counter-measures.
Conditioning in white rats and suppression of a hemisphere's cortex with spreading depression revealed that the right hemisphere prevailed in perception of space, in the simultaneous information processing, in perception of concrete signs and in deductive processing whereas the left hemisphere was predominant in perception of time, in successive information processing, in perception of abstract signs and in inductive processing. Induction and deduction are hypothetically assumed to be the main factors determining the lateralization of functions in the brain hemispheres.
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UNLABELLED: The contribution of vestibular and neck inputs to the perception of visual object motion in space was studied in the absence of a visual background (in the dark) in normal human subjects (Ss). Measures of these contributions were obtained by means of a closed loop nulling procedure; Ss fixed their eyes on a luminous spot (object) and nulled its actual or apparent motion in space during head rotation in space (vestibular stimulus) and/or trunk rotation relative to the head (neck stimulus) with the help of a joystick. Vestibular and neck contributions were expressed in terms of gain and phase with respect to the visuo-oculomotor/joystick feedback loop which was assumed to have almost ideal transfer characteristics. The stimuli were applied as sinusoidal rotations in the horizontal plane (f = 0.025-0.8 Hz; peak angular displacements, 1-16 degrees). RESULTS: (1) During vestibular stimulation, Ss perceived the object, when kept in fixed alignment with the moving body, as moving in space. However, they underestimated the object motion; the gain was only about 0.7 at 0.2-0.8 Hz and clearly decreased at lower stimulus frequencies, while the phase exhibited a small lead. (2) During pure neck stimulation (trunk rotating relative to the stationary head), the object, when stationary, appeared to move in space counter to the trunk excursion. This neck-contingent object motion illusion was small at 0.2-0.8 Hz, but increased considerably with decreasing frequency, while its phase developed a small lag. (3) Vestibular, neck, and visuo-oculomotor effects summed linearly during combined stimulations. (4) The erroneous vestibular and neck contributions to the object motion perception were complementary to each other, and the perception became about veridical (G approximately 1, phi approximately 0 degree), when both inputs were combined during head rotation with the trunk stationary. The results are simulated by an extended version of a computer model that previously had been developed to describe vestibular and neck effects on human perception of head motion in space. In the model, the perception of object motion in space is derived from the superposition of three signals, representing "object to head" (visuo-oculomotor; head coordinates), "head on trunk" (neck; trunk coordinates), and "trunk in space" (vestibular-neck interaction; space coordinates).
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Gattass and collaborators (Gattass R, Rosa MGP, Souza APB, Piñon MCG, Neuenschwander S [1990a] Braz J Med Biol Res 23:375-393) proposed that the dorsal stream of visual processing, as defined by Ungerleider and Mishkin (Ungerleider LG, Mishkin M [1982] In: Ingle DJ, Goodale MA, Mansfield RJW, editors. Analysis of visual behavior. Cambridge: Massachusetts Institute of Technology. p 549-586), can be subdivided into dorsolateral and dorsomedial streams, and suggested that they may be involved in different aspects of the processing of motion and spatial perception, respectively. The goal of the present study was to provide additional evidence for this hypothesis by using cytochrome oxidase immunohistochemistry combined with retrograde tracing techniques. In Old World monkeys, the locations of visual area 4 (V4; ventral stream) and middle temporal area (MT; dorsal stream) projecting neurons in V2 supports the hypothesis that the cytochrome oxidase (CytOx)-rich thin stripes and the CytOx-poor interstripes are associated with the ventral stream, and that the CytOx-rich thick stripes belong to the dorsal stream. In this study we describe, in the New World monkey Cebus, the distribution of retrogradely labeled cells in V2 relative to the CytOx compartments after fluorescent tracers were placed in areas V4, MT, and the parietooccipital area (PO). We found PO-projecting neurons in CytOx-rich thick stripes and CytOx-poor interstripes in V2, whereas MT-projecting neurons appeared almost exclusively in thick stripes. In contrast, V4-projecting neurons were located mostly in CytOx-poor interstripes and CytOx-rich thin stripes. In addition, V4- and MT-projecting neurons were located mainly in supragranular layers, whereas PO-projecting neurons were located in supragranular and infragranular layers. These results support the hypothesis for the existence of three distinct streams of visual processing: ventral (including V4), dorsolateral (including MT), and dorsomedial (including PO).
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For each of 74 simple striate cells a quantitative analysis was made of the width dimensions and spatial arrangements of the subregions responding either at light on (ON subregion) or at light off (OFF subregion). It was concluded that every cell has at least two and no more than four subregions. Cells with two subregions (57%) were much more commonly encountered than those with three (32%) or four (11%). For most cells adjacent subregions were significantly overlapped, the region of overlap responding both at light on and at light off. In the case of cells with two subregions, the overlap averaged 32% of the overall width of the two subregions. Despite the degree of the overlap, there was, on this basis, still a large measure of discrimination between cells in the simple family and those in the B-cell and complex families. In general the receptive field profiles of cells with three and four subregions were only marginally wider than those with only two subregions. In any given receptive field, the subregions tend to be roughly equal in width so that, in cells with four subregions, the subregions are, on the average, distinctly narrower than they are in cells with only two. Hypercomplex I cells tend to have receptive fields with three and four subregions much more commonly than simple cells and these cells are encountered much more frequently in cortical cell laminae 2, 3 and 4 than in lamina 6. In lamina 6 most of the cells in the simple family have receptive fields with only two subregions. The width dimensions and spatial sequences of the response peaks to moving light and dark edges were quantitatively analyzed in response profiles prepared from 82 cells. In general, for any given receptive field, the response peaks to moving edges have a one-to-one correspondence with the subregions to a stationary flashing bar. When this is not the case, the tendency is for the number of response peaks to edges to be less than the number of subregions rather than more.
We have characterized the speed of response of simple cells in cat striate cortex by the temporal phase of the response to bar and grating stimuli. Stimulation of the most responsive subregion (either ON or OFF) in the receptive field with a 1 Hz temporally modulated bar elicited responses whose phase led the excitatory phase of the stimulus by about 25 degrees. The response to stationary gratings whose contrast was sinusoidally modulated at 2 Hz also showed a phase lead. The differences in the phase of response of ON and OFF sub-regions exhibited a marked scatter about the expected value of 180 degrees. The phase of response to both temporally modulated bars and laterally moving gratings advanced by 20-35 degrees as the stimulus contrast was raised by a factor of 5.
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Threshold illumination levels, It, for visual detection of white light targets, moving across spatially structured background fields, have been measured and it is shown that, for a given background illumination level, It depends upon the spatial characteristics of the background field structure. Thus, with the background composed of a square-waveform grating of fundamental spatial frequency f cycles/deg, It is maximum for an intermediate value of f, and falls as f increases or decreases from this value. The relationship between It and f characterizes the interaction between movement detection and the background grating, and is designated the IMG function. The parametric properties of the IMG functions are described and it is established that the mechanisms which give rise to these functions are sensitive to the movement, but not the spatial structure of the target. They correspond, therefore, to the movement-sensitive Y-type mechanisms, observed in electrophysiological studies of cat and primate visual pathways. The spatial distribution of sensitivity associated with the IMG functions has been computed by 2-D transform methods, the computation yielding circularly symmetric, centre-surround antagonistic "receptive field" distributions.
The retinal location of a saccadic target was made discrepant with its perceived position by means of an induced displacement. If localizing the target required information stored in memory, the eye was directed to the perceived target position. Otherwise, it was directed to its retinal location. These findings do not conform to either a strictly retinotopic or spatiotopic model of oculomotor control. Rather they suggest that the position information used to program saccades may be either perceptual or retinal/spatial depending upon whether the information must be accessed from memory.
Experimental findings concerning the properties of the phenomenon of mislocation of brief visual stimuli during smooth eye tracking are described. One of these, which cannot be explained by existing hypotheses, is that under certain conditions the mislocation magnitude tends to have zero or even negative values. A model is developed for explanation of the mislocation phenomenon. It is suggested that localization is based on: (1) information about the current eye position and (2) information about the stimulus locus on the retina. They both arrive at the localization centre with non-zero delays. The mode of information processing in this centre leads to a magnitude of mislocation which is proportional to the difference between the two delays and which could be positive, zero or negative. Factors which influence either delay should also influence the mislocation magnitude.
In a series of recent experiments we have examined the effects of varying the spatio-temporal determinants of some motion configurations on the geometric properties of the perceived motions. For both apparent motion and the kinetic depth effect (being two representative motion sources) specific spatio-temporal frequency and phase limits have been determined with respect to the various (geometrically defined) percepts Finally, a network is proposed which enables predictions about perceived motion loci (and other geometric features), based on the equating of the observed spatio-temporal limits with the bandwidth for a filtering mechanism.
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