Sport Skill–Specific Expertise Biases Sensory Integration for Spatial Referencing and Postural Control

The authors asked how sport expertise modulates visual field dependence and sensory reweighting for controlling posture. Experienced soccer athletes, ballet dancers, and nonathletes performed (a) a Rod and Frame test and (b) a 100-s bipedal stance task during which vision and proprioception were successively or concurrently disrupted in 20-s blocks. Postural adaptation was assessed in the mean center of pressure displacement, root mean square of center of pressure velocity and ankle muscles integrated electromyography activity. Soccer athletes were more field dependent than were nonathletes. During standing, dancers were more destabilized by vibration and required more time to reweigh sensory information compared with the other 2 groups. These findings reveal a sport skill–specific bias in the reweighing of sensory inputs for spatial orientation and postural control.     

Effects of Voluntary and Automatic Control of Center of Pressure Sway During Quiet Standing

The authors investigated the effects of voluntary and automatic control on the spatial variables (envelope area, maximal amplitude, and root mean square [RMS]) of center of pressure (COP) displacement during quiet standing and identified differences in their postural control strategies (mean velocity [MV], mean power frequency [MPF], and power density). COP data were recorded under relaxed (experimental control), still (voluntary control), and dual (automatic control) conditions. RMS was significantly lower in the still and dual conditions than in the relaxed condition. MV, MPF, and power density were significantly higher in the still condition than in the dual condition. These results indicate that both voluntary and automatic control decrease the spatial variables of COP displacement; however, their postural control strategies are different.     

New motion illusion caused by pictorial motion lines

Motion lines (MLs) are a pictorial technique used to represent object movement in a still picture. This study explored how MLs contribute to motion perception. In Experiment 1, we reported the creation of a motion illusion caused by MLs: random displacements of objects with MLs on each frame were perceived as unidirectional global motion along the pictorial motion direction implied by MLs. In Experiment 2, we showed that the illusory global motion in the peripheral visual field captured the perceived motion direction of random displacement of objects without MLs in the central visual field, and confirmed that the results in Experiment 1 did not stem simply from response bias, but resulted from perceptual processing. In Experiment 3, we showed that the spatial arrangement of orientation information rather than ML length is important for the illusory global motion. Our results indicate that the ML effect is based on perceptual processing rather than response bias, and that comparison of neighboring orientation components may underlie the determination of pictorial motion direction with MLs.     

Remapping versus short-term memory in visual stability across saccades

Saccadic eye movements cause displacements of the image of the visual world projected on the retina. Despite the ubiquitous nature of saccades, subjective experience of the world is continuous and stable. In five experiments, we addressed the mechanisms that may support visual stability: matching of pre- and postsaccadic locations of the target by an internal copy of the saccade, or retention of the visual attributes of the target in short-term memory across the saccade. Healthy human adults were instructed to make a saccade to a peripheral Gabor patch. While the saccade was in midflight, the patch could change location, orientation, or both. The change occurred either immediately or following a 250-ms blank during which no visual stimuli were available. In separate experiments, subjects had to report either whether the patch stepped to the left or right or whether the orientation rotated clockwise or counterclockwise. Consistent with previous findings, we found that transsaccadic displacement discrimination was enhanced by the addition of the blank. However, contrary to previous findings reported in the literature, the feature change did not improve performance. Transsaccadic orientation change discrimination did not depend on either an irrelevant temporal blank or a simultaneous irrelevant target displacement. Taken together, these findings suggest that orientation is not a relevant visual feature for transsaccadic correspondence.     

Effects of joint immobilization on standing balance

We investigated the effect of joint immobilization on the postural sway during quiet standing. We hypothesized that the center of pressure (COP), rambling, and trembling trajectories would be affected by joint immobilization. Ten young adults stood on a force plate during 60 s without and with immobilized joints (only knees constrained, CK; knees and hips, CH; and knees, hips, and trunk, CT), with their eyes open (OE) or closed (CE). The root mean square deviation (RMS, the standard deviation from the mean) and mean speed of COP, rambling, and trembling trajectories in the anterior–posterior and medial–lateral directions were analyzed. Similar effects of vision were observed for both directions: larger amplitudes for all variables were observed in the CE condition. In the anterior–posterior direction, postural sway increased only when the knees, hips, and trunk were immobilized. For the medial–lateral direction, the RMS and the mean speed of the COP, rambling, and trembling displacements decreased after immobilization of knees and hips and knees, hips, and trunk. These findings indicate that the single inverted pendulum model is unable to completely explain the processes involved in the control of the quiet upright stance in the anterior–posterior and medial–lateral directions.     

Representational momentum in spatial hearing

The final position of a moving visual object usually appears to be displaced in the direction of motion. We investigated this phenomenon, termed representational momentum, in the auditory modality. In a dark anechoic environment, an acoustic target (continuous noise or noise pulses) moved from left to right or from right to left along the frontal horizontal plane. Listeners judged the final position of the target using a hand pointer. Target velocity was 8 degrees s(-1) or 16 degrees s(-1). Generally, the final target positions were localised as displaced in the direction of motion. With presentation of continuous noise, target velocity had a strong influence on mean displacement: displacements were stronger with lower velocity. No influence of sound velocity on displacement was found with motion of pulsed noise. Although these findings suggest that the underlying mechanisms may be different in the auditory and visual modality, the occurrence of displacements indicates that representational-momentum-like effects are not restricted to the visual modality, but may reflect a general phenomenon with judgments of dynamic events.     

Binocular unmasking with vertical disparity

We recently found (Schneider, Moraglia, & Jepson, 1989) that the contrast threshold for the detection of a visual signal in a noisy background can be considerably lower when binocular cues are available then when monocular cues only are present. Here, we investigated the occurrence of binocular unmasking with vertical interocular disparities. Subjects reported about the presence of Gabor signals in fields of two-dimensional broadband Gaussian noise surrounded by a frame of uniform noise. They saw these stimuli through a stereoscope; in all cases, the right-eye noise field was vertically displaced relative to the left one in either an upward or a downward direction, by up to 67.6'. In one condition, the right-eye signal was displaced by an amount equal to that of the noise, so that no opportunities for binocular unmasking existed; in the other, it appeared in exactly corresponding locations in the two fields--here, binocular disparities could be used to unmask the signal. Enhanced signal detectability, by up to 12.7 dB, was observed in the latter case for both directions of displacement, but only for displacements of 13.52' and only when the signal's orientation was horizontal. We argue that these effects result from the summation of monocular inputs carried out by linear binocular mechanisms.     

Saccadic suppression of displacement: effects of illumination and background manipulation

In contrast to other functions which are suppressed during saccades, saccadic suppression of displacement (SSD--a decrease in sensitivity to visual displacements during saccades) has often been considered to be due to efferent processes rather than to visual masking. The aim of this study was to explicitly assess the importance of visual conditions in SSD. In two experiments, a small computer-generated target made random horizontal jumps. An infrared eye tracker was used to detect the saccade toward the new position, triggering a smaller centripetal displacement of the target. Subjects reported awareness of these intrasaccadic displacements by pressing a key. In the first experiment, the task was performed in both a well-lit environment and in darkness. In the second experiment these conditions were replicated and additional factors such as the contrast of the background and the effect of moving the target spot alone or the target plus the entire background were investigated. Unlike other forms of saccadic suppression, SSD was stronger in the dark, although subjects also had a greater bias to report detections in that condition. Other background manipulations had no effect. The effect of ambient lighting on SSD is small and subtle. Effects of other background manipulations may be overridden by the focusing of attention on a small moving target.     

Perception of motion in equiluminous kinematograms

Two fields of random dots that were identical except for a slight shift in a central square region were presented in rapid alternation. This produced a vivid impression of a square moving back and forth above the background. When the kinematogram is presented in equiluminous red/green, the motion of the central region can still be seen, although over a narrower range of alternation rates, interstimulus intervals, and displacements than for black/white presentation. The perception of motion for equiluminous stimuli indicates that colour and motion can be analyzed conjointly by the visual system. However, as originally reported by Ramachandran and Gregory, the segregation of the oscillating central square from the background is lost at equiluminance. This segregation process therefore appears to be colour-blind.     

The orientation anisotropy and orientation constancy: a visual evoked potential study.

Two experiments were conducted on the orientation anisotropy in which averaged visual evoked potentials (VEPs) were recorded from the occipital scalp. The first experiment confirmed the findings of Maffei and Campbell (1970) that obliquely oriented gratings alternated back and forth produced smaller-amplitude VEPs than when the gratings were oriented horizontally or vertically. Since no asymmetry was found in VEPs produced by a Julesz figure presented under identical conditions, it was concluded that direction of displacement could not have been contributing to the effect. In a second experiment head tilt of the subject was manipulated together with grating orientation and the results indicated that the orientation anisotropy is retinally rather than gravitationally referenced. It was concluded that the site of orientation constancy is located either at higher levels of the primary visual system or in the second visual system.     

The integration of orientation information in the motion correspondence problem

We examine how differently oriented components contribute to the discrimination of motion direction along a horizontal axis. Stimuli were two-frame random-dot kinematograms that were narrowband filtered in spatial frequency. On each trial, subjects had to state whether motion was to the left or the right. For each stimulus condition, Dmax (the largest displacement supporting 80% correct direction discrimination performance) was measured. In experiment 1, Dmax was measured for orientationally narrowband stimuli as a function of their mean orientation. Dmax was found to increase as the orientation of the stimuli became closer to the axis of motion. Experiment 2 used isotropic stimuli in which some orientation bands contained a coherent motion signal, and some contained only noise. When the noise band started at vertical orientations and increased until only horizontal orientations contained a coherent motion signal, Dmax increased slightly. This suggests that near-vertical orientations interfere with motion perception at large displacements when they contain a coherent motion signal. When the noise band started at horizontal and increased until only vertical orientations contained the motion signal, Dmax decreased steadily. This implies that Dmax depends at least partly on the most horizontal motion signal in the stimulus. These results were contrasted with two models. In the first, the visual system utilises the most informative orientations (nearest horizontal). In the second, all available orientations are used equally. Results supported an intermediate interpretation, in which all orientations are used but more informative ones are weighted more heavily.     

Transient stimulation does not aid visual search: Implications for the role of saccades

Previous demonstrations that performance on visual search tasks with briefly flashed presentations declines over time after the initial onset imply that saccades might be necessary for efficient acquisition of visual information. We imposed an additional abrupt onset and a displacement on character arrays containing letters and one numeral while subjects searched for the numeral. Presentations were always followed by a visual noise field. Presentation time varied (50–800 msec). We found that performance with presentations containing one onset and remaining continuously visible was better than performance with presentations containing two onsets and containing displacements. Furthermore, information acquired near the onset of a continuous presentation was as effective as information acquired later. Our results demonstrate that abrupt onsets and displacements do not improve information acquisition with displays of alphanumeric characters. This finding is consistent with earlier reports that saccade-like retinal image motion does not contribute either to the maintenance of target visibility or to visual acuity.     

The time course of perceptual choice: the leaky, competing accumulator model

The time course of perceptual choice is discussed in a model of gradual, leaky, stochastic, and competitive information accumulation in nonlinear decision units. Special cases of the model match a classical diffusion process, but leakage and competition work together to address several challenges to existing diffusion, random walk, and accumulator models. The model accounts for data from choice tasks using both time-controlled (e.g., response signal) and standard reaction time paradigms and its adequacy compares favorably with other approaches. A new paradigm that controls the time of arrival of information supporting different choice alternatives provides further support. The model captures choice behavior regardless of the number of alternatives, accounting for the log-linear relation between reaction time and number of alternatives (Hick's law) and explains a complex pattern of visual and contextual priming in visual word identification.     

Visual search for expressions and anti-expressions

We used visual search to explore whether the preattentive mechanisms that enable rapid detection of facial expressions are driven by visual information from the displacement of features in expressions, or other factors such as affect. We measured search slopes for luminance and contrast equated images of facial expressions and anti-expressions of six emotions (anger, fear, disgust, surprise, happiness, and sadness). Anti-expressions have an equivalent magnitude of facial feature displacements to their corresponding expressions, but different affective content. There was a strong correlation between these search slopes and the magnitude of feature displacements in expressions and anti-expressions, indicating feature displacement had an effect on search performance. There were significant differences between search slopes for expressions and anti-expressions of happiness, sadness, anger, and surprise, which could not be explained in terms of feature differences, suggesting preattentive mechanisms were sensitive to other factors. A categorization task confirmed that the affective content of expressions and anti-expressions of each of these emotions were different, suggesting signals of affect might well have been influencing attention and search performance. Our results support a picture in which preattentive mechanisms may be driven by factors at a number of levels, including affect and the magnitude of feature displacement. We note that indirect effects of feature displacement, such as changes in local contrast, may well affect preattentive processing. These are most likely to be nonlinearly related to feature displacement and are, we argue, an important consideration for any study using images of expression to explore how affect guides attention. We also note that indirect effects of feature displacement (for example, changes in local contrast) may well affect preattentive processing. We argue that such effects are an important consideration for any study using images of expression to explore how affect guides attention.     

Influences of the perception of self-motion on postural parameters.

We examined how spatial and temporal characteristics of the perception of self-motion, generated by constant velocity visual motion, was reflected in orientation of the head and whole body of young adults standing in a CAVE, a virtual environment that presents wide field of view stereo images with context and texture. Center of pressure responses from a force plate and perception of self-motion through orientation of a hand-held wand were recorded. The influence of the perception of self-motion on postural kinematics differed depending upon the plane and complexity of visual motion. Postural behaviors generated through the perception of self-motion appeared to contain a confluence of the cortically integrated visual and vestibular signals and of other somatosensory inputs. This would suggest that spatial representation during motion in the environment is modified by both ascending and descending controls. We infer from these data that motion of the visual surround can be used as a therapeutic tool to influence posture and spatial orientation, particularly in more visually sensitive individuals following central nervous system (CNS) impairment.     

The effects of visual input on postural control of the lumbar spine in unstable sitting

Postural control of the lumbar spine in unstable sitting was quantified through the analysis of the center of pressure (CoP) movement recorded by a force plate situated underneath a seat that incorporated a hemisphere. Thirteen healthy subjects were tested under conditions of increasing seat instability and elimination of visual input. The purpose of this study was to determine the relative effects of visual input and support surface instability on open and closed loop postural control mechanisms in sitting and to determine the association between traditional summary statistics and random walk analysis of CoP movement. The effects of the seat instability level and visual input on the CoP movement parameters were tested with a two-factor, repeated measures ANOVA (p<0.01). In all summary statistics CoP movement parameters increased significantly due to the seat instability level and lack of visual input. The random walk analysis identified two regions, short- and long-term, which has been postulated to represent open and closed loop control mechanism, respectively. While short-term scaling exponents were independent from visual input, CoP displacement in the short-term region was significantly increased in the eyes closed condition. Summary statistic of CoP total path length per second correlated highly with critical point coordinates and short-term diffusion coefficients. The CoP movement in the long-term region was consistent with a closed loop control mechanisms. The findings of visual influence on what is assumed as an open-loop control mechanism does not, at face value, support the hypothesis that two separate mechanisms are working to achieve postural control.     

THE VISUAL SYSTEM'S MEASUREMENT OF INVARIANTS NEED NOT ITSELF BE INVARIANT

Abstract— When two shapes that differ in orientation or size have to be compared or objects have to be recognized from different viewpoints, the response time and error rate art systematically affected by the size of the geometric difference. In this report, we argue that these effects are not necessarily solid evidence for the use of mental transformations and against the use of invariants by the visual system. We report an experiment in which observers were asked to give affine-invariant coordinates of a point located in an affine frame defined by three other points. The angle subtended by the coordinate axes and the ratio of the lengths of their unit vectors systematically affected the measurement errors. This finding demonstrates that the visual system's measurement of invariants need not itself be invariant.     

The angle of visual roll motion determines displacement of subjective visual vertical

The effect of full-field sinusoidal visual roll motion stimuli of various frequencies and peak velocities upon the orientation of subjective visual vertical (SV) was studied. The angle of the optokinetically induced displacement of SV was found to be a linear function of the logarithm of the stimulus oscillation angle. Interindividual slopes of this function varied between 2 and 9. The logarithmic function is independent of stimulus frequency within the range of .02 Hz to .5 Hz and of peak stimulus velocity from 7.5°/sec to 170°/sec. It holds for oscillation angles up to 100°–140°. With larger rotational angles, saturation is reached. With small stimulus angles, a surprisingly high threshold (5°-8°) was observed in our experiments. This may reflect the unphysiological combination of visual roll stimuli without corroborating vestibular and proprioceptive inputs normally present when body sway produces visual stimulation. Under natural conditions, the visual feedback about spontaneous sway stabilizes body posture by integrating rotational velocity over stimulus duration which is equal to rotational angle.     

State reversals of optically induced tilt and torsional eye movements

Alternations of the state of apparent self-motion during observation of a large visual display rotating about the line of sight are associated with alternations in the magnitude of induced tilt and torsional eye rotation. In one experiment, shifts in visually induced tilt during these state alternations are found to be in the opposite direction to corresponding shifts in induced ocular torsion. In a second experiment, the reversals of self-motion perception are shown to be an intravisual phenomenon, independent of competing inputs provided by the vestibular system. These results emphasize the importance of distinguishing between visual and vestibular processes in tilt perception and ocular rotation during human orientation to gravitational vertical.