Effects of up-down visual inversion on motor skills

The movement of a hand or fingers and locomotion of the body by a subject wearing prisms which inverted his visual world were investigated. A subject wore frame-spectacles (without prisms) for the first two days and then wore up-down inverting spectacles (with prisms) for the next four days, followed by wearing the former frame-spectacles again for one day. Measurements were made of skill on star-drawing, pegboard tests, and on zigzag-walking and walking up and down stairs. There were no differences on the five measures during acquisition for the four tasks, which suggests smooth progress of prism-adaptation by this man.     

Autokinetic movement and inverted vision

It was considered that inverted vision could influence the condition of the subject's relative framework. The aim of this study was to investigate whether autokinetic movement observed during inverted vision might differ from that in normal vision. One subject wearing inverting spectacles and another one subject in normal vision observed autokinetic movement for five days. The results showed that directional changes increased with the time spent in visual inversion, while in normal vision such tendency was not observed. One speculative interpretation was suggested in terms of subject-related framework.     

Effects of living in the up-down inverted visual world on apparent movement

The purpose of this study was to examine whether a change of perceptual framework may affect the occurrence of apparent movement. Apparent movement was observed by one subject living over four days in the prismatically inverted visual world, because this situation was considered as the operation in which the subject was forced to change the perceptual framework to adapt himself to the novel environment. Apparent movement with two points was measured in vertical and horizontal configurations before wearing and after removing the prism as well as while wearing it. Analysis showed significant effects of prism-wearing on the occurrence of apparent movement in both vertical and horizontal configurations. Although further elaboration is required, an hypothesis was suggested from the viewpoint of the loss of visual position constancy.     

MOVEMENT AND DISTORTION IN VISUAL PATTERNS DURING PROLONGED FIXATION

H onisett , J., and O ldfield , R. C. Movement and distortion in visual patterns during prolonged fixation. Scand. J. Psychol ., 1960, 2 , 49–55.—Observations are reported from which it appears that if fixation upon a single point in a complex visual field is maintained for periods of half a minute or more a proportion of normal individuals experience movement of the whole field or of parts of it. Changing distortions of form and pattern can result. Some types of this movement are, it is thought, improbably due to intrinsic or extrinsic ocular changes, and more resemble the autokinetic phenomenon. It is suggested that eye-movements and their visual consequences are indispensable to the maintenance of a stable coordinate system in the visual world.     

The position of random autokinetic movement and the physiological position of rest are frequently stable and identical

Both the autokinetic illusion (AKI) and involuntary eye movements when a fixation point goes off have been attributed to unmonitored drift eye movements which result from constant features of the oculomotor system. Pilot studies confirmed that the visual directions where these effects had no directional bias, the position of random autokinetic movement (PRAKM) and the physiological position of rest (PPR), were highly correlated and reliable. The more precise main experiment showed that they were usually, but not always, stable and identical. Drifts are therefore not totally due to stable features of the oculomotor system but are a compound of several slow responses which can differ with both stimulus conditions and time. They are not all equally unmonitored.     

Self-selected visual information during discrete manual aiming

The authors examined strategic selection of visual samples during manual aiming. Participants (N = 12) wore liquid-crystal goggles while performing discrete movements to a small target. Initially, participants controlled a 40-ms visual sample via a switch in their nonaiming hand. Subsequently, experimenter-imposed strategies required participants to take visual samples before movement initiation or early or late in the movement. Although participants adopted a variety of strategies to optimize the use of vision, they were more likely to select a sample during the early stages of the movement. Experimenter-imposed early and late instructions resulted in longer movement times than did self-selected sampling. Compared with late sampling, early sampling resulted in a temporal advantage with similar accuracy.     

Self-Selected Visual Information During Discrete Manual Aiming

The authors examined strategic selection of visual samples during manual aiming. Participants (N = 12) wore liquid-crystal goggles while performing discrete movements to a small target. Initially, participants controlled a 40-ms visual sample via a switch in their nonaiming hand. Subsequently, experimenter-imposed strategies required participants to take visual samples before movement initiation or early or late in the movement. Although participants adopted a variety of strategies to optimize the use of vision, they were more likely to select a sample during the early stages of the movement. Experimenter-imposed early and late instructions resulted in longer movement times than did self-selected sampling. Compared with late sampling, early sampling resulted in a temporal advantage with similar accuracy.     

Effects of target-background luminance ratios upon the autokinetic illusion

This study investigated effects of the target-background luminance ratios upon the autokinetic illusion, with special emphasis on manipulation of the background intensity. Exp. 1, in which the effects of four levels of target luminance were examined against the completely dark background, showed that the target luminance did not affect the illusion as long as the target was small enough in size (0.17 degrees in visual angle). This result confirmed the suggestion by Edwards in 1954. In Exp. II effects of the target-background luminance ratios were examined by varying the luminance of target and background independently. Dominant illusory patterns at the luminance ratio 1 were "pendulum-like" and "bobbing"; these differed from those at higher ratios ("winding"). On the other hand, latency and duration were not affected by the ratios. These findings suggest that the movement pattern is effective in specifying the autokinetic illusion, if it is appropriately categorized and represented.     

Effects of Pointing Rate and Availability of Visual Feedback on Visual and Proprioceptive Components of Prism Adaptation

While looking through laterally displacing prisms, subjects pointed 60 times straight ahead of their nose at a rate of one complete movement every 2 or 3 s, with visual feedback available early in the pointing movement or delayed until the end of the movement. Sagittal pointing was paced such that movement speed covaried with pointing rate. Aftereffect measures (obtained after every 10 pointing trials) showed that when the limb became visible early in a pointing movement, proprioceptive adaptation was greater than visual, but when visual feedback was delayed until the end of the movement, the reverse was true. This effect occurred only with the 3-s pointing rate, however. With the 2-s pointing rate, adaptation was predominately proprioceptive in nature, regardless of feedback availability. Independent of the availability of visual feedback, visual adaptation developed more quickly with 3-s pointing, whereas proprioceptive adaptation developed more rapidly with 2-s pointing. These results are discussed in terms of a model of perceptual-motor organization in which the direction of coordinative (guidance) linkage between eye-head (visual) and hand-head (proprioceptive) systems (and consequently the locus of discordance registration and adaptive recalibration) is determined jointly by pointing rate and feedback availability. An additional effect of pointing rate is to determine the rate of discordant inputs. Maximal adaptive recalibration occurs when the input (pointing) rate matches the time constant of the adaptive encoder in the guided system.     

The influence of stimulus array on training of a speeded response

We conducted two experiments to study the training of speeded responses to stimuli in a clock face array. Participants were trained on one clock face and later tested on either the same or a different clock face. The clock faces varied along 3 dimensions of change (left-right flip, up-down flip, and 180 degrees rotation). Skill acquisition was reflected in decreases in overall, initiation, and movement response times in the training and test phases except that movement time reached an asymptote during training and did not decrease further during test. Test performance was best when training and test used the same clock face and worst when the training to test change involved an up-down flip. The transition to different clock faces was consistent with an interpretation based on the violation of expectations about target positions acquired during training. Consistent trial-by-trial feedback led to better initiation time but not movement time during training than periodic feedback, but this effect did not persist into the test phase.     

Effects of Movement Duration and Visual Feedback on Visual and Proprioceptive Components of Prism Adaptation

While looking through laterally displacing prisms, subjects pointed sagittally 80 times at an objectively straight-ahead target, completing a reciprocal out-and-back pointing movement every 1, 3, or 6 s. Visual feedback was available early in the pointing movement or only late at the end of movement. Aftereffect measures of adaptive shift (obtained after every 10 pointing trials) showed adaptive change only in limb position sense (i.e., proprioceptive adaptation) when movement duration was 1 s, regardless of visual feedback condition; but as movement duration increased, adaptive change in the eye position sense (i.e., visual adaptation) increased while proprioceptive adaptation decreased, especially for the late visual feedback condition. Regardless of visual feedback condition, proprioceptive adaptation showed the maximal rate of growth with the 1-s movement duration, whereas visual adaptation showed maximal growth with the 6-s movement duration. These results provide additional support for a model of adaptive spatial mapping in which the direction of strategically flexible coordination (guidance) between eye and limb (and consequently the locus of adaptive spatial mapping) is jointly determined by movement duration and timing of visual feedback. An additional effect of movement duration is to determine the rate of discordant inputs. Maximal growth of adaptation occurs when the input rate matches the response time of the spatial mapping function.     

Effects of movement duration and visual feedback on visual and proprioceptive components of prism adaptation

While looking through laterally displacing prisms, subjects pointed sagittally 80 times at an objectively straight-ahead target, completing a reciprocal out-and-back pointing movement ever 1, 3, or 6 s. Visual feedback was available early in the pointing movement or only late at the end of the movement. Aftereffect measures of adaptive shift (obtained after every 10 pointing trials) showed adaptive change only in limb position sense (i.e., proprioceptive adaptation) when movement duration was 1 s, regardless of visual feedback condition; but as movement duration increased, adaptive change in the eye position sense (i.e., visual adaptation) increased while proprioceptive adaptation decreased, especially for the late visual feedback condition. Regardless of visual feedback condition, proprioceptive adaptation showed the maximal rate of growth with the 1-s movement duration, whereas visual adaptation showed maximal growth with the 6-s movement duration. These results provide additional support for a model of adaptive spatial mapping in which the direction of strategically flexible coordination (guidance) between eye and limb (and consequently the locus of adaptive spatial mapping) is jointly determined by movement duration and timing of visual feedback. An additional effect of movement duration is to determine the rate of discordant inputs. Maximal growth of adaptation occurs when the input rate matches the response time of the spatial mapping function.     

Children's autokinetic movement as a function of inferred movement of target shape

Four target shapes, a control stimulus (circle) and one each representing geometrical (arrow), representational (car), and symbolic (cross) implied movement were presented to 10 children in each of five age groups of boys and girls (4, 6, 8, 10, 12 yr.) in an autokinetic movement task. While there were no differences in direction of perceived movement with regard to the control stimulus (circle), all other target shapes showed a decrease in the effects of implied movement with increases in age. The minor sex differences were not reported.     

Oculomotor adaptation to prisms is not simply a muscle potentiation effect

An experiment is reported in which subjects pointed to a visual target before and after exposure to prisms. The exposure condition required the subject to look at his feet through leftward deviating prisms while holding his eyes to the right. Aftereffects on pointing were significantly to the right. This result is opposite to that predicted by the muscle potentiation hypothesis put forward by Ebenholtz and Wolfson (1975), but consistent with recalibration of the visual direction system caused by spatial discordance.     

Paradoxical sleep and information processing: exploration by inversion of the visual field

The purpose of this study was to test the potential relationship between REM sleep and information processing with inversion of the visual field. In the first experiment, four male subjects slept in the laboratory for two sessions of 6 consecutive nights: 2 adaptation nights, 2 nights of polysomnography, and 2 nights of dream collection. During the days preceding Nights 3, 4, 5, and 6 of each session, the subjects wore glasses which, during the second session, completely inverted (rotation of 180 degrees) their visual field. In a second experiment with four other male subjects, the order of conditions was reversed, and the experimental condition (visual inversion) was introduced a second time. When the data of the two experiments were combined, there was a significant (p less than .01) increase in the percentage of REM sleep from Nights 3 and 4 of the control condition to Nights 3 and 4 of the visual inversion condition, but there was no significant change in any of the other sleep stages. There was a significant decrease in horizontal (p less than .04) and vertical (p less than .005) REM density and in the density of vertical REM bursts (p less than .02). The increase in REM sleep supports the hypothesis that REM sleep contributes to information processing while the decrease in REM density suggests that this component of REM sleep may be involved in a homeostatic process of sensory input.     

Adaptation to vertical displacement of the visual direction

Sixty Ss wore vertically displacing wedge prisms and adapted by looking at their feet for 10 min. Half of them did this while standing and the others in supine position. The latter condition produced adaptation measurable with a visual-motor test and with a test of egocentric localization, but on a purely motoric test no adaptation was apparent. Standing during the adaptation period produced no effect.     

Cognitive Load and Prism Adaptation

Subjects wore goggles with prisms that laterally displaced the visual field (rightward by 11.4 degree) and with full view of the limb engaged in paced (2-s rate) sagittal pointing at either an implicit ("straight ahead of the nose") target (Experiment 1) or an explicit (positioned leftward by 11.4 degree) target (in Experiment 2). In experimental conditions, subjects performed a secondary cognitive task (mental arithmetic) simultaneously during target pointing. In control conditions, no cognitive load was imposed. Aftereffect measures of adaptation to the prismatic displacement were not substantially different when problem solving was required, but terminal error of the exposure pointing task was reliably affected by cognitive load. These results are consistent with the hypothesis of separable mechanisms for adaptive coordination and adaptive alignment. Adaptive coordination may be mediated by strategically flexible coordinative linkage between sensory motor systems (eye-head and hand-head), but spatial alignment seems to be mediated by adaptive encoders within coordinatively linked subsystems. If the coordination task involves predominately automatic processing, coordinative linkage can be frequent enough under cognitive load for substantial realignment to occur even though exposure performance (adaptive coordination) may be less than optimal.     

Effects of interlimb practice on coding and learning of movement sequences

An interlimb practice paradigm was designed to determine the role that visual–spatial (Cartesian) and motor (joint angles, activation patterns) coordinates play in the coding and learning of complex movement sequences. Participants practised a 16-element movement sequence by moving a lever to sequentially presented targets with one limb on Day 1 and the contralateral limb on Day 2. Practice involved the same sequence with either the same visual–spatial or motor coordinates on the two days. A unilateral practice condition (control) was also tested where both coordinate systems were changed but the same limb was used. Retention tests were conducted on Day 3. Regardless of the order in which the limbs were used during practice, results indicated that keeping the visual–spatial coordinates the same during acquisition resulted in superior retention. This provides strong evidence that the visual–spatial code plays a dominant role in complex movement sequences, and this code is represented in an effector-independent manner.     

Cognitive Load and Prism Adaptation

Subjects wore goggles with prisms that laterally displaced the visual field (rightward by 11.4°) and with full view of the limb engaged in paced (2-s rate) sagittal pointing at either an implicit (“straight ahead of the nose”) target (Experiment 1) or an explicit (positioned leftward by 11.4°) target (in Experiment 2). In experimental conditions, subjects performed a secondary cognitive task (mental arithmetic) simultaneously during target pointing. In control conditions, no cognitive load was imposed. Aftereffect measures of adaptation to the prismatic displacement were not substantially different when problem solving was required, but terminal error of the exposure pointing task was reliably affected by cognitive load. These results are consistent with the hypothesis of separable mechanisms for adaptive coordination and adaptive alignment. Adaptive coordination may be mediated by strategically flexible coordinative linkage between sensory–motor systems (eye–head and hand—head), but spatial alignment seems to be mediated by adaptive encoders within coordinatively linked subsystems. If the coordination task involves predominately automatic processing, coordinative linkage can be frequent enough under cognitive load for substantial realignment to occur even though exposure performance (adaptive coordination) may be less than optimal.     

Autokinesis direction during and after eye turn

The aftereffect (AE) of eye turn on autokinesis direction is usually, but not always, opposite to the inducing turn direction. During four experiments, a model predicting the aftereffect’s time course and a new measure utilizing the concept of the position of random autokinetic movement (PRAKM) were developed. They showed that aftereffect direction alternates during dissipation and that its first direction is not a simple function of previous eye position, but of the process by which that position is achieved, suggesting that at least two processes are involved. In one S, versions produced the usual AE, while, after vergences, the AE was in the same direction as the inducing turn. Differential recruitment of these systems in monocular fixation could account for individual differences in the AE.