Exploring the Limits of Peripheral Vision for the Control of Movement

The role played by peripheral visual information in the control of aiming movements is not fully understood, as is indicated by the conflicting results reported in the literature. In the present study, the authors tested and confirmed the hypothesis that the source of the conflict lies in the portion of the visual peripheral field that has been under scrutiny in the different studies. Participants (N = 60) moved a computer mouse from a fixed starting position to 1 of 3 targets under varied vision conditions. The portion of the peripheral visual field that best ensured directional accuracy of a sweeping movement was found to be located between 20° and 10° of visual angle, whereas the area found to favor directional accuracy of an aiming movement comprised 30° through 10° of visual angle.     

Exploring the limits of peripheral vision for the control of movement

The role played by peripheral visual information in the control of aiming movements is not fully understood, as is indicated by the conflicting results reported in the literature. In the present study, the authors tested and confirmed the hypothesis that the source of the conflict lies in the portion of the visual peripheral field that has been under scrutiny in the different studies. Participants (N = 60) moved a computer mouse from a fixed starting position to 1 of 3 targets under varied vision conditions. The portion of the peripheral visual field that best ensured directional accuracy of a sweeping movement was found to be located between 20 degrees and 10 degrees of visual angle, whereas the area found to favor directional accuracy of an aiming movement comprised 30 degrees through 10 degrees of visual angle.     

Flank to the left,flank to the right: Testing the modified receptive field hypothesis of letter-specific crowding

The present study tested for effects of number of flankers positioned to the left and to the right of target characters as a function of visual field and stimulus type (letters or shapes). On the basis of the modified receptive field hypothesis (Chanceaux & Grainger, 2012), we predicted that the greatest effects of flanker interference would occur for leftward flankers with letter targets in the left visual field. Target letters and simple shape stimuli were briefly presented and accompanied by either 1, 2, or 3 flankers of the same category either to the left or to the right of the target, and in all conditions with a single flanker on the opposite side. Targets were presented in the left or right visual field at a fixed eccentricity, such that targets and flankers always fell into the same visual field. Results showed greatest interference for leftward flankers associated with letter targets in the left visual field, as predicted by the modified receptive field hypothesis.     

Attention effects on form discrimination at different eccentricities

Considerable disagreement exists in the visual attention literature about how attention is allocated over the visual field. One frequently expressed metaphor is that attention moves like a spotlight, and in some variants it is assumed that attention takes longer to shift to targets further from fixation. In order to test this metaphor, five experiments were conducted in which target location was precued and form discrimination accuracy was assessed. By varying the interval between the precue and the target (stimulus onset asynchrony, SOA), a time course of attention effects was obtained for targets at 2°, 6°, and 10° eccentricity. In the first three experiments, precueing effects were found, but there were no differences in performance as a function of eccentricity for very short SOAs, with either a peripheral cue or a foveal arrow cue. For long SOAs, however, performance was better for targets that were closer to fixation. In Experiments 4 (peripheral cue) and 5 (foveal cue), the targets were scaled to make them equally discriminable at all eccentricities. Again precueing effects were found, but there were no differences in accuracy as a function of eccentricity for most SOAs. These results suggest that attention shifting is not analogous to a constant-velocity moving spotlight.     

Afferent Information for Motor Control: The Role of Visual Information in Different Portions of the Movement

The question addressed in the present study was whether subjects (N = 24) can use visual information about their hand, in the first half of an aiming movement, to ensure optimal directional accuracy of their aiming movements. Four groups of subjects practiced an aiming task in either a complete vision condition, a no-vision condition, or in a condition in which their hand was visible for the first half [initial vision condition (IV)] or the second half of the movement [final vision condition (FV)]. Following 240 trials of acquisition, all subjects were submitted to a transfer test that consisted of 40 trials performed in a no-vision condition. The results indicated that seeing the hand early in movement did not help subjects to optimize either directional or amplitude accuracy. On the other hand, when subjects viewed their hand closer to the target, movements resulted that were as accurate as those performed under a complete vision condition. In transfer, withdrawing vision did not cause any increase in aiming error for the IV or the no-vision conditions. These results replicated those of Carlton (1981) and extended those of Bard and colleagues (Bard, Hay, & Fleury, 1985) in that they indicated that the kinetic visual channel hypothesized by Paillard (1980; Paillard & Amblard, 1985) appeared to be inoperative beyond 40deg of visual angle.     

Head flexion and different walking speeds do not affect gait stability in older females

Head flexion is destabilizing in older individuals during quiet stance, yet the effect head flexion has on gait is not known. The study examined whether head flexion and gait parameters were altered when walking freely and fixed to a visual target, at different walking speeds. 15 young (23 ± 4 years) and 16 older (76 ± 6 years) healthy females walked at three different walking speeds (slow, comfortable, and fast) under two visual conditions (natural and fixed [focusing on a visual target set at eye level]). Head flexion was assessed using 2D video analysis, whilst gait parameters (step length, double support time, step time, and gait stability ratio) were recorded during a 9 m flat walkway. A mixed design ANOVA was performed for each variable, with age as the between-subject factor and, visual condition and walking speed as within-subject factors. When walking freely, older displayed a greater need for head flexion between walking speeds (P < 0.05) when compared to young. Walking under fixed condition reduced head flexion at all walking speeds in the older (P < 0.05), but had no effect on the young (P > 0.05). Walking at different speeds showed no difference in head flexion when walking under either visual condition and had no effect on gait stability for both groups. Despite older displaying differences in head flexion between visual conditions, there was no effect on gait parameters. Walking speed presented trivial difference in head flexion in older females, whilst overall gait stability was unaffected by different walking speeds.     

Response times and eye movements in feature and conjunction search as a function of target eccentricity

In four experiments, saccadic eye movements, reaction times (RTs), and accuracy were measured as observers searched for feature or conjunction targets presented at several eccentricities. A conjunction search deficit, evidenced by a large eccentricity effect on RTs, accuracy, and number of saccades, was seen in Experiments 1A and 1B. Experiment 2 indicated that, when saccades were precluded, there was an even larger eccentricity effect for conjunction search targets. In Experiment 3, practice in a conjunction search task allowed both RT and number of saccades to become independent of eccentricity. Additionally, there was evidence of feature-based selectivity in that observers were more likely to fixate distractors that had the same contrast as the target. Results are consistent with the view that the oculomotor and attentional systems are functionally linked and provide constraints for models of visual attention and search.     

Evidence Supporting the Importance of Peripheral Visual Information for the Directional Control of Aiming Movement

The focus of the present study was on determining whether the high level of directional accuracy found in aiming studies in which the subjects can see their hand in the visual periphery supports the existence of a kinetic visual channel or, rather, the advantage of binocular over monocular vision for movement directional control. The limits of this kinetic visual channel were also explored. The results of the 1st experiment indicated that seeing one's hand in the visual periphery is sufficient to ensure optimal directional aiming accuracy. Further, no differences in aiming accuracy were noted between monocular and binocular vision. These results supported the existence of a visual kinetic channel. In the 2nd experiment, whether this kinetic visual channel would operate with movements slower (55°/s) than those usually used in studies that had proved its existence (over 110°/s) was determined. The results indicated that this visual kinetic channel was operative even at relatively slow movement velocities. Central vision of the hand seemed to be used for on-line directional control of relatively slow movements.     

Why are there eccentricity effects in visual search? Visual and attentional hypotheses

In standard visual search experiments, observers search for a target item among distracting items. The locations of target items are generally random within the display and ignored as a factor in data analysis. Previous work has shown that targets presented near fixation are, in fact, found more efficiently than are targets presented at more peripheral locations. This paper proposes that the primary cause of this “eccentricity effect” (Carrasco, Evert, Chang, & Katz, 1995) is an attentional bias that allocates attention preferentially to central items. The first four experiments dealt with the possibility that visual, and not attentional, factors underlie the eccentricity effect. They showed that the eccentricity effect cannot be accounted for by the peripheral reduction in visual sensitivity, peripheral crowding, or cortical magnification. Experiment 5 tested the attention allocation model and also showed that RT X set size effects can be independent of eccentricity effects. Experiment 6 showed that the effective set size in a search task depends, in part, on the eccentricity of the target because observers search from fixation outward.     

Visual information: The control of aiming movements

The study examined the contribution of various sources of visual information utilised in the control of discrete aiming movements. Subjects produced movements, 15.24 cm in amplitude, to a 1.27 cm target in a movement time of 330 ms. Responses were carried out at five vision-manipulation conditions which allowed the subject complete vision, no vision, vision of only the target or stylus, and a combination of stylus and target. Response accuracy scores indicated that a decrement in performance occurred when movements were completed in the absence of visual information or when only the target was visible during the response. The stylus and the target plus stylus visual conditions led to response accuracy which was comparable to movements produced with complete vision. These results suggest that the critical visual information for aiming accuracy is that of the stylus. These findings are consistent with a control model based on a visual representation of the discrepancy between the position of the hand and the location of the target.     

Colavita dominance effect revisited: the effect of semantic congruity

To investigate the effect of semantic congruity on audiovisual target responses, participants detected a semantic concept that was embedded in a series of rapidly presented stimuli. The target concept appeared as a picture, an environmental sound, or both; and in bimodal trials, the audiovisual events were either consistent or inconsistent in their representation of a semantic concept. The results showed faster detection latencies to bimodal than to unimodal targets and a higher rate of missed targets when visual distractors were presented together with auditory targets, in comparison to auditory targets presented alone. The findings of Experiment 2 showed a cross-modal asymmetry, such that visual distractors were found to interfere with the accuracy of auditory target detection, but auditory distractors had no effect on either the speed or the accuracy of visual target detection. The biased-competition theory of attention (Desimone & Duncan Annual Review of Neuroscience 18: 1995; Duncan, Humphreys, & Ward Current Opinion in Neurobiology 7: 255–261 1997) was used to explain the findings because, when the saliency of the visual stimuli was reduced by the addition of a noise filter in Experiment 4, visual interference on auditory target detection was diminished. Additionally, the results showed faster and more accurate target detection when semantic concepts were represented in a visual rather than an auditory format.     

Evidence Supporting the Importance of Peripheral Visual Information for the Directional Control of Aiming Movement

The focus of the present study was on determining whether the high level of directional accuracy found in aiming studies in which the subjects can see their hand in the visual periphery supports the existence of a kinetic visual channel or, rather, the advantage of binocular over monocular vision for movement directional control. The limits of this kinetic visual channel were also explored. The results of the 1st experiment indicated that seeing one's hand in the visual periphery is sufficient to ensure optimal directional aiming accuracy. Further, no differences in aiming accuracy were noted between monocular and binocular vision. These results supported the existence of a visual kinetic channel. In the 2nd experiment, whether this kinetic visual channel would operate with movements slower (55 degrees /s) than those usually used in studies that had proved its existence (over 110 degrees /s) was delineated. The results indicated that this visual kinetic channel was operative even at relatively slow movement velocities. Central vision of the hand seemed to be used for on-line directional control of relatively slow movements.     

The role of the right hemisphere in speech act comprehension

In this research the role of the RH in the comprehension of speech acts (or illocutionary force) was examined. Two split-screen experiments were conducted in which participants made lexical decisions for lateralized targets after reading a brief conversation remark. On one-half of the trials the target word named the speech act performed with the preceding conversation remark; on the remaining trials the target did not name the speech act that the remark performed. In both experiments, lexical decisions were facilitated for targets representing the speech act performed with the prior utterance, but only when the target was presented to the left visual field (and hence initially processed by the RH) and not when presented to the right visual field. This effect occurred at both short (Experiment 1: 250 ms) and long (Experiment 2: 1000 ms) delays. The results demonstrate the critical role played by the RH in conversation processing.     

Effects of prime—target spatial separation and attentional deployment on masked repetition priming

In two masked repetition priming experiments with letter stimuli, the positions of prime and target stimuli were varied horizontally from fixation. Priming effects did not interact with position when prime and target location covaried (Experiment 1A) but diminished with increasing prime eccentricity when targets were always centrally located (Experiment 1B). Two accounts of this pattern of priming effects were proposed that postulate two different mechanisms over and above effects of visual acuity. The integration account postulates degree of separation of prime and target stimuli as the critical factor, and the attentional account postulates spatial attention as the critical factor. The results of Experiment 2, in which prime and target positions were manipulated orthogonally, were in favor of the attentional account. Repetition priming did not vary as a function of whether or not primes and targets appeared at the same location, but target processing was facilitated independently of priming when targets appeared at the same location as primes, especially in the right visual field.     

Combined visual illusion effects on the perceived index of difficulty and movement outcomes in discrete and continuous fitts’ tapping

The speed-accuracy trade-off is a fundamental movement problem that has been extensively investigated. It has been established that the speed at which one can move to tap targets depends on how large the targets are and how far they are apart. These spatial properties of the targets can be quantified by the index of difficulty (ID). Two visual illusions are known to affect the perception of target size and movement amplitude: the Ebbinghaus illusion and Muller-Lyer illusion. We created visual images that combined these two visual illusions to manipulate the perceived ID, and then examined people’s visual perception of the targets in illusory context as well as their performance in tapping those targets in both discrete and continuous manners. The findings revealed that the combined visual illusions affected the perceived ID similarly in both discrete and continuous judgment conditions. However, the movement outcomes were affected by the combined visual illusions according to the tapping mode. In discrete tapping, the combined visual illusions affected both movement accuracy and movement amplitude such that the effective ID resembled the perceived ID. In continuous tapping, none of the movement outcomes were affected by the combined visual illusions. Participants tapped the targets with higher speed and accuracy in all visual conditions. Based on these findings, we concluded that distinct visual-motor control mechanisms were responsible for execution of discrete and continuous Fitts’ tapping. Although discrete tapping relies on allocentric information (object-centered) to plan for action, continuous tapping relies on egocentric information (self-centered) to control for action. The planning-control model for rapid aiming movements is supported.     

Effects of prime-target spatial separation and attentional deployment on masked repetition priming

In two masked repetition priming experiments with letter stimuli, the positions of prime and target stimuli were varied horizontally from fixation. Priming effects did not interact with position when prime and target location covaried (Experiment 1A) but diminished with increasing prime eccentricity when targets were always centrally located (Experiment 1B). Two accounts of this pattern of priming effects were proposed that postulate two different mechanisms over and above effects of visual acuity. The integration account postulates degree of separation of prime and target stimuli as the critical factor, and the attentional account postulates spatial attention as the critical factor. The results of Experiment 2, in which prime and target positions were manipulated orthogonally, were in favor of the attentional account. Repetition priming did not vary as a function of whether or not primes and targets appeared at the same location, but target processing was facilitated independently of priming when targets appeared at the same location as primes, especially in the right visual field.     

Determining the Temporal Limits of a Visual Sample for Visual Regulation

The author examined the minimum amount of time needed for vision to increase aiming accuracy and decrease movement duration. Participants selected when they would receive a visual sample during aiming movements by pressing a switch held with the left hand. The sample was one of the following durations: 40 ms, 30 ms, 20 ms, 10 ms, or 0 ms (no vision). Decreased accuracy in the no-vision condition compared to the vision conditions was observed when the duration of the impending sample was unknown (Experiment 1). Samples 40 ms in duration were sufficient to decrease endpoint variability when the duration of the sample was known before the movement (Experiment 2). These results indicate that short visual samples can be used to decrease movement time and increase accuracy and that knowledge of the impending visual context can impact the individual's subsequent behavior.     

Modeling spatial effects in visualtactile saccadic reaction time

Saccadic reaction time (SRT) to visual targets tends to be shorter when nonvisual stimuli are presented in close temporal or spatial proximity, even when subjects are instructed to ignore the accessory input. Here, we investigate visualtactile interaction effects on SRT under varying spatial configurations. SRT to bimodal stimuli was reduced by up to 30 msec, in comparison with responses to unimodal visual targets. In contrast to previous findings, the amount of multisensory facilitation did not decrease with increases in the physical distance between the target and the nontarget but depended on (1) whether the target and the nontarget were presented in the same hemifield (ipsilateral) or in different hemifields (contralateral), (2) the eccentricity of the stimuli, and (3) the frequency of the vibrotactile nontarget. The time-window-of-integration (TWIN) model for SRT (Colonius & Diederich, 2004) is shown to yield an explicit characterization of the observed multisensory spatial interaction effects through the removal of the peripheral-processing effects of stimulus location and tactile frequency.     

Manual localization of lateralized visual targets

The effects of visual field, responding limb and extrapersonal space on the ability to localize visual targets using slow positioning movements of the arm were examined. Special contact lenses were used to lateralize visual information and to make comparisons with localization under monocular control conditions. Subjects made slow positioning movements to place a cursor directly beneath target lights. They saw target lights but not the moving limb during the trial. For directional error, results indicated that subjects were more accurate localizing targets lateralized to the right hemisphere than targets lateralized to the left hemisphere, indicating right hemisphere superiority for localization of visual targets in grasping space. Localization performance was significantly better with the right hand than the left hand. the left hand demonstrated a directional bias to the right of the targets. Responding hand and visual field did not interact. Finally, contrary to subjects' awareness and verbal reports, target localization was not less accurate in lens than in monocular control conditions. This was true for both amplitude and directional error. This is consistent with other studies where visual information about limb position is not available.     

Targets of the memorized position and visual contexts]

The goal of this study was to determine whether a sensorimotor or cognitive encoding is used to encode a target position and save it into iconic memory. The methodology consisted of disrupting a manual aiming movement to a memorized visual target by displacing the visual field containing the target. The nature of the encoding was inferred from the nature and the size of the errors relative to a control. The target was presented either centrally or in the right periphery. Participants moved their hand from the left to the right of fixation. Black and white vertical stripes covered the whole visual field. The visual field was either stationary throughout the trial or was displaced to the right or left at the extinction of the target or at the start of the hand movement. In the latter case, the displacement of the visual field obviously could only be taken into account by the participant during the gesture. In this condition, our hypothesis was that the aiming error would follow the direction of visual field displacement. Results showed three major effects: (1) Vision of the hand during the gesture improved the final accuracy; (2) visual field displacement produced an underestimation of the target distance only when the hand was not visible during the gesture and was always in the same direction displacement; and (3) the effect of the stationary structured visual field on aiming precision when the hand was not visible depended on the distance to the target. These results suggest that a stationary structured visual field is used to support the memory of the target position. The structured visual field is more critical when the hand is not visible and when the target appears in peripheral rather than central vision. This suggests that aiming depends on memory of the relative peripheral position of the target (allocentric reference). However, in the present task, cognitive encoding does not maintain the "position" of the target in memory without reference to the environment. The systematic effect of the visual field displacement on the manual aiming suggests that the role of environmental reference frames in memory for position is not well understood. Some studies, in particular those of Giesbrecht and Dixon (1999) and Glover and Dixon (2001), suggested differing roles of the environment in the retention of the target position and the control of aiming movements toward the target. The present observations contribute to understanding the mechanism involved in locating and grasping objects with the hand.