Changes in straight-ahead eye position during adaptation to wedge prisms

If S is instructed to look straight ahead before adapting to laterally displaced vision, he does so without noticeable error. After adapting, however, in response to the same instruction, he may rotate his eyes as much as 8° toward the the displaced visual target. This is the change in judgment of the direction of gaze which Helmholtz identified in 1867 as an important physiological mechanism in adaptation to prisms. It leads to more accurate reaching behavior by causing S to make a visual judgment that the target is closer to straight ahead than it was when he first looked through the prisms. This type of adaptive change (change in judgment of the direction of gaze, oculomotor change) can be measured either by manual judgments (difference between successive “straight ahead” and “visual target” judgments) or by changes in straight-ahead eye position. It may be described as a parametric adjustment in the oculomotor control system, and is closely analogous to the eye movement which subserves the recovery of binocular fusion in prism vergence.     

Speed-Accuracy Characteristics of Saccadic Eye Movements

Speed-accuracy trade-off characteristic of horizontal saccadic eye movements were examined in this study. Unlike limb movements, saccadic eye movements are preprogrammed, unidimensional, and do not involve target impact. Hence, they provide an optimal test of the impulse variability account of the speed-accuracy trade-off in rapid movements. Subjects were required to alternately look at two target lights as fast and as accurately as possible for a period of 10 s. Target lights subtended angles of 5,10,15, and 20°. By restricting target distances to less than 20° of arc, the speed-accuracy relation was examined for single horizontal saccadic movements of the eye. Movement of the dominant eye was tracked with an infra-red eye monitoring device. Fifty saccadic movements of the eye were recorded for each target distance and used to compute the average amplitude, duration, and velocity of eye movements, as well as, movement endpoint variability. An increase in both average velocity and movement endpoint variability with increasing movement amplitude was found. This, together with the unique features of the eye movement system, support the impulse variability account of the speed-accuracy trade-off in rapid movements.     

Our Eyes Do Not Always Go Where We Want Them to Go: Capture of the Eyes by New Objects

Observers make rapid eye movements to examine the world around them. Before an eye movement is made, attention is covertly shifted to the location of the object of interest. The eyes typically will land at the position at which attention is directed. Here we report that a goal-directed eye movement toward a uniquely colored object is disrupted by the appearance of a new but task-irrelevant object, unless subjects have a sufficient amount of time to focus their attention on the location of the target prior to the appearance of the new object. In many instances, the eyes started moving toward the new object before gaze started to shift to the color-singleton target. The eyes often landed for a very short period of time (25–150 ms) near the new object. The results suggest parallel programming of two saccades: one voluntary, goal-directed eye movement toward the color-singleton target and one stimulus-driven eye movement reflexively elicited by the appearance of the new object. Neuroanatomical structures responsible for parallel programming of saccades are discussed.     

Exploiting human sensitivity to gaze for tracking the eyes

Given the prevalence, quality, and low cost of web cameras, along with the remarkable human sensitivity to gaze, we examined the accuracy of eye tracking using only a web camera. Participants were shown webcamera recordings of a person’s eyes moving 1°, 2°, or 3° of visual angle in one of eight radial directions (north, northeast, east, southeast, etc.), or no eye movement occurred at all. Observers judged whether an eye movement was made and, if so, its direction. Our findings demonstrate that for all saccades of any size or direction, observers can detect and discriminate eye movements significantly better than chance. Critically, the larger the saccade, the better the judgments, so that for eye movements of 3°, people can tell whether an eye movement occurred, and where it was going, at about 90% or better. This simple methodology of using a web camera and looking for eye movements offers researchers a simple, reliable, and cost-effective research tool that can be applied effectively both in studies where it is important that participants maintain central fixation (e.g., covert attention investigations) and in those where they are free or required to move their eyes (e.g., visual search).     

Intentionally-evoked modulations of smooth pursuit eye movements

When observers pursue a moving target with their eyes, they use predictions of future target positions in order to keep the target within the fovea. It was suggested that these predictions of smooth pursuit (SP) eye movements are computed only from the visual feedback of the target characteristics. As a consequence, if the target vanishes unexpectedly, the eye movements do not stop immediately, but they overshoot the vanishing point. We compared the spatial and temporal features of such predictive eye movements in a task with or without intentional control over the target vanishing point. If the observers stopped the target with a button press, the overshoot of the eyes was reduced compared to a condition where the offset was computer generated. Accordingly, the eyes started to decelerate well before the target offset and lagged further behind the target when it disappeared. The involvement of intentionally-generated expectancies in eye movement control was also obvious in the spatial trajectories of the eyes, which showed a clear flexion in anticipation of the circular motion path we used. These findings are discussed together with neurophysiological mechanisms underlying the SP eye movements.     

Direction-specific motion thresholds for abnormal image shifts during saccadic eye movement

Eye movements were monitored and a target circle subtending an angle of 7^o was made to move during and dependent on the eye movements. Thresholds of detection of the resulting abnormal image displacements were obtained. Thresholds were low when both the eyes and the target moved either horizontally or vertically. They were higher by a factor of two or more when the eye movements and the target motions were not in the same plane. In the latter conditions, two processes account for the detection of target motion. One is a compensation process where the extent of that component of the motion of the retinal image of the target which is parallel to the eye movement is compared with the extent of the eye movement. The other process detects an angle between the plane of the target image motion and the plane of the eye movement. Our results indicate that the higher thresholds occurred when detection of this angle was required.     

Attending to a misoriented word causes the eyeball to rotate in the head

Torsional eye movements are triggered by head tilt and a rotating visual field. We examined whether attention to a misoriented form could also induce torsion. Thirty-six observers viewed an adapting field containing a bright vertical Une, and then they viewed a display that was composed of two misoriented words (one rotated clockwise, the other counterclockwise, by 15°, 30°, or 45°). The subjects were instructed to attend to one of the words. The subjects’ adjustments of a reference line to match the tilt of the afterimage showed that attention to a misoriented word produces torsional eye movement (verified with direct measurements on 4 additional subjects). This eye movement reduces the retinal misorientation of the word by about 1°. The results of this study reinforce the linkage between selective attention and eye movements and may provide a useful tool for dissecting different forms of “mental rotation” and other adjustments in internal reference frames. Apparent-motion displays confirming that the eye rotated in the head may be downloaded from www.psychonomic.org/archive.     

Eye-hand coordination in goal-directed aiming.

In a number of studies, we have demonstrated that the spatial-temporal coupling of eye and hand movements is optimal for the pickup of visual information about the position of the hand and the target late in the hand's trajectory. Several experiments designed to examine temporal coupling have shown that the eyes arrive at the target area concurrently with the hand achieving peak acceleration. Between the time the hand reached peak velocity and the end of the movement, increased variability in the position of the shoulder and the elbow was accompanied by a decreased spatial variability in the hand. Presumably, this reduction in variability was due to the use of retinal and extra-retinal information about the relative positions of the eye, hand and target. However, the hand does not appear to be a slave to the eye. For example, we have been able to decouple eye movements and hand movements using Müller-Lyer configurations as targets. Predictable bias, found in primary and corrective saccadic eye movements, was not found for hand movements, if on-line visual information about the target was available during aiming. That is, the hand remained accurate even when the eye had a tendency to undershoot or overshoot the target position. However, biases of the hand were evident, at least in the initial portion of an aiming movement, when vision of the target was removed and vision of the hand remained. These findings accent the versatility of human motor control and have implications for current models of visual processing and limb control.     

How do we know what we are doing? Time, intention and awareness of action

Time is a fundamental dimension of consciousness. Many studies of the "sense of agency" have investigated whether we attribute actions to ourselves based on a conscious experience of intention occurring prior to action, or based on a reconstruction after the action itself has occurred. Here, we ask the same question about a lower level aspect of action experience, namely awareness of the detailed spatial form of a simple movement. Subjects reached for a target, which unpredictably jumped to the side on some trials. Participants (1) expressed their expectancy of a target shift during the upcoming movement, (2) pointed at the target as quickly and accurately as possible before returning to the start posiment to the target shift if required and (3) reproduced the spatial path of the movement they had just made, as accurately as possible, to give an indication of their awareness of the pointing movement. We analysed the spatial disparity between the initial and the reproduced movements on those with a target shift. A negative disparity value, or undershoot, suggests that motor awareness merely reflects a sluggish record of coordinated motor performance, while a positive value, or overshoot, suggests that participants' intention to point to the shifting target contributes more to their awareness of action than their actual pointing movement. Undershoot and overshoot thus measure the reconstructive (motoric) and the preconstuctive (intentional) aspects of action awareness, respectively. We found that trials on which subjects strongly expected a target shift showed greater overshoot and less undershoot than trials with lower expectancy. Conscious expectancy therefore strongly influences the experience of the detailed motor parameters of our actions. Further, a delay inserted either between the expectancy judgement and the pointing movement, or between the pointing movement and the reproduction of the movement, had no effect on visuomotor adjustment but strongly influenced action awareness. Delays during either interval boosted undershoots, suggesting increased reliance on a time-limited sensory memory for action. The experience of action is thus strongly influenced by prior thoughts and expectations, but only over a short time period. Thus, awareness of our actions is a dynamic and relatively flexible mixture of what we intend to do, and what our motor system actually does.     

Interactions between goal-directed eye and arm movements: arguments for an interdependent motor control

The accuracy of movements of the arm directed toward a point in space was investigated in healthy human subjects. To study the influence of the eye movement itself, on the guidance of the arm in the absence of any visual context, subjects performed the goal-directed arm movements without visual feedback about the arm displacement and the target position. The subjects were asked either to keep their eyes centered or oriented toward a previously flashed target. The analysis of the distribution of the errors in arm final position in the two conditions suggests that the eye movement influences the final position adopted by the arm. It is postulated that an interaction exists between the eye and arm systems during the motor program elaboration phase.     

Development of binocular fixation in human infants

Two experiments measured changes in binocular eye alignment from 1- to 6-month-old human infants. In Experiment 1 changes in binocular eye alignment were recorded from 1, 2, and 3 month olds using corneal photography. A luminous target was moved along the infant's midline at one of two constant speeds. Infants at all three ages showed some evidence of appropriate changes in binocular eye alignment (convergence as the target approached and divergence as the target receded). The likelihood of appropriate convergence and divergence increased with age, as did the ability to respond appropriately to the faster target motion. A measure of convergence lag (further decrease in interpupillary distance after target motion had ended) was obtained for trials on which the target approached the infant. Convergence lag decreased with age and was greater on trials at the faster target speed until 3 months of age. Experiment 2 measured the responses of 3, $\text{4}\text{1}\text{2}$, and 6 month olds as a wedge prism was placed alternately in front of each eye. The prism displaced the image nasally (either 2.5° or 5°), creating inappropriate binocular eye alignment. A refixation eye movement in response to the prism was not present consistently until 6 months of age. Hypotheses as to the mechanism controlling infant binocular eye alignment are discussed with respect both to the present findings and to findings from human adults and animals.     

An investigation of the relationship between eye and retinal image movement in the perception of movement

The question investigated was whether or not eye movements accompanied by abnormal retinal image movements, movements that are either or both at a different rate or in a different direction than the eye movement, predictably lead to perceived movement. Os reported whether or not they saw a visual target move when the movement of the target was either dependent on and simultaneous with their eye movements or when the target movement was independent of their eye movements. In the main experiment, observations were made when the ratio between eye and target movement fem/tm) was 2/5, 1/5, 1/10, 1/20, and 0. All these ratios were tested when the direction of the target movement was in the same (H+), opposite (H?), and at right angles to (V+, V?) the movement of the eyes. Eye movements, target movements, and reports of target movement were recorded. Results indicate that a discrepancy between eye and target movement greater than 20% predictably leads to perceived target movement, whereas a discrepancy of 5% or less rarely leads to perceived movement. The results are interpreted as support for the operation of a compensatory mechanism during eye movements.     

Attentional localization prior to simple and directed manual responses

The relationship between attention and the programming of motor responses was investigated, using a paradigm in which the onsets of targets for movements were preceded by peripheral attentional cues. Simple (button release) and reaching manual responses were compared under conditions in which the subjects either made saccades toward the target location or refrained from making eye movements. The timing of the movement onset was used as the dependent measure for both simple and reaching manual responses. Eye movement latencies were also measured. A follow-up experiment measured the effect of the same peripheral cuing procedure on purely visual processes, using signal detection measures of visual sensitivity and response bias. The results of the first experiment showed that reaction time (RT) increased with the distance between the cued and the target locations. Stronger distance effects were observed when goal-directed responses were required, which suggests enhanced attentional localization of target positions under these conditions. The requirement to generate an eye movement response was found to delay simple manual RTs. However, mean reaching RTs were unaffected by the eye movement condition. Distance gradients on eye movement latencies were relatively shallow, as compared with those on goal-directed manual responses. The second experiment showed that the peripheral cue had only a very small effect on visual detection sensitivity in the absence of directed motor responses. It is concluded that cue-target distance effects with peripheral cues are modulated by the motor-programming requirements of the task. The effect of the peripheral cue on eye movement latencies was qualitatively different from that observed on manual RTs, indicating the existence of separate neural representations underlying both response types. At the same time, the interactions between response modalities are consistent with a supramodal representation of attentional space, within which different motor programs may interact.     

Attentional localization prior to simpleand directed manual responses

The relationship between attention and the programming of motor responses was investigated, using a paradigm in which the onsets of targets for movements were preceded by peripheral attentional cues. Simple (button release) and reaching manual responses were compared under conditions in which the subjects either made saccades toward the target location or refrained from making eye movements. The timing of the movement onset was used as the dependent measure for both simple and reaching manual responses. Eye movement latencies were also measured. A follow-up experiment measured the effect of the same peripheral cuing procedure on purely visual processes, using signal detection mea-sures of visual sensitivity and response bias. The results of the first experiment showed that reaction time (RT) increased with the distance between the cued and the target locations. Stronger distance ef-fects were observed when goal-directed responses were required, which suggests enhanced attentional localization of target positions under these conditions. The requirement to generate an eye movement response was found to delay simple manual RTs. However, mean reaching RTs were unaffected by the eye movement condition. Distance gradients on eye movement latencies were relatively shallow, as compared with those on goal-directed manual responses. The second experiment showed that the peripheral cue had only a very small effect on visual detection sensitivity in the absence of directed motor responses. It is concluded that cue-target distance effects with peripheral cues are modulated by the motor-programming requirements of the task. The effect of the peripheral cue on eye movement latencies was qualitatively different from that observed on manual RTs, indicating the existence of separate neural representations underlying both response types. At the same time, the interactions be-tween response modalities are consistent with a supramodal representation of attentional space, within which different motor programs may interact.     

Brightness as a function of retinal locus

Brightness functions were determined for the dark-adapted fovea and periphery. In one series of experiments, observers matched numbers to the brightness of a 1° white target at various intensities, presented half the time to the fovea, the other half to one of five peripheral loci: 5°, 12°, 20°, 35°, and 60°. In a second series, observers matched the brightness of a 1° white target in the fovea of one eye to the brightness of an identical target in the periphery of the other eye at various intensities. Thresholds were also determined for the fovea and for the five peripheral loci by a staircase procedure. The magnitude estimations and the interocular matches concur in showing that a stimulus of fixed luminance appears brighter in the periphery than in the fovea. The brightness was found to be maximal at 20°. Brightness grows as a similar power function of luminance at all six retinal positions.     

Brightness as a function of retinal locus

Brightness functions were determined for the dark-adapted fovea and periphery. In one series of experiments, observers matched numbers to the brightness of a 1° white target at various intensities, presented half the time to the fovea, the other half to one of five peripheral loci: 5°, 12°, 20°, 35°, and 60°. In a second series, observers matched the brightness of a 1° white target in the fovea of one eye to the brightness of an identical target in the periphery of the other eye at various intensities. Thresholds were also determined for the fovea and for the five peripheral loci by a staircase procedure. The magnitude estimations and the interocular matches concur in showing that a stimulus of fixed luminance appears brighter in the periphery than in the fovea. The brightness was found to be maximal at 20°. Brightness grows as a similar power function of luminance at all six retinal positions.     

Visual stability with goal-directed eye and arm movements toward a target displaced during saccadic suppression

This experiment tested whether the perceived stability of the environment is altered when there is a combination of eye and visually open-loop hand movements toward a target displaced during the eye movements, i.e., during saccadic suppression. Visual-target eccentricity randomly decreased or increased during eye movements and subjects reported whether they perceived a target displacement or not, and if so, the direction of the displacement. Three experimental conditions, involving different combinations of eye and arm movements, were tested: (a) eye movements only; (b) simultaneous eye and rapid arm movements toward the target; and (c) simultaneous eye and arm movements with a restraint blocking the arm as soon as the hand left the starting position. The perceptual threshold of target displacements resulting in an increased target eccentricity was greater when subjects combined eye and arm movements toward the target object, specially for the no-restraint condition. Subjects corrected most of their arm trajectory toward the displaced target despite the short movement times (average MT = 189 ms). After the movements, the null error feedback of the hand's final position presumably overlapped the retino-oculomotor signal error and could be responsible for the deficient perception of target displacements. Thus, subjects interpreted the terminal hand positions as being within the range of the endpoint variability associated with the production of rapid arm movements rather than as a change of the environment. These results suggest that a natural strategy adopted for processing spatial information, especially in a competing situation, could favour a constancy tendency, avoiding systematic perception of a change of environment for any noise or variability at the central or peripheral levels.     

Searching for a word in Chinese text: insights from eye movement behaviour

Locating relevant information in text is an important aspect of the reading process, however relatively few studies have examined this, especially for logographic languages such as Chinese. The present study examines eye movement behaviour during search for a target word in Chinese sentences, compared with reading the sentences for comprehension. Although there were clear effects of word frequency during reading for comprehension, the study shows no evidence for an influence of the word frequency of non-target words on eye movement behaviour during target word search. The results are in line with previous research undertaken in English (Rayner, K., & Fischer, M. H. (1996). Mindless reading revisited: Eye movements during reading and scanning are different. Perception & Psychophysics, 58, 734–747.), such that during search for a target word, eye movement behaviour for non-target words is largely driven by superficial processing of those words. The study also highlights the prevalence of word skipping, indicating that words are often sampled only in visually degraded parafoveal vision during target word search in Chinese.     

Colour and spatial cueing in low-prevalence visual search

People are able to judge the current position of occluded moving objects. This operation is known as motion extrapolation. It has previously been suggested that motion extrapolation is independent of the oculomotor system. Here we revisited this question by measuring eye position while participants completed two types of motion extrapolation task. In one task, a moving visual target travelled rightwards, disappeared, then reappeared further along its trajectory. Participants discriminated correct reappearance times from incorrect (too early or too late) with a two-alternative forced-choice button press. In the second task, the target travelled rightwards behind a visible, rectangular occluder, and participants pressed a button at the time when they judged it should reappear. In both tasks, performance was significantly different under fixation as compared to free eye movement conditions. When eye movements were permitted, eye movements during occlusion were related to participants' judgements. Finally, even when participants were required to fixate, small changes in eye position around fixation (<2°) were influenced by occluded target motion. These results all indicate that overlapping systems control eye movements and judgements on motion extrapolation tasks. This has implications for understanding the mechanism underlying motion extrapolation.     

Eye movements and time-based selection: Where do the eyes go in preview search?

In visual search tasks, presenting one set of distractors (previewing them) before a second set which contains the target, improves search efficiency compared to when all items appear simultaneously. It has been proposed that this preview benefit reflects an attentional bias against old information and toward new information. Here we tested directly whether there was such a bias by measuring eye movement behavior. The main findings were that fixations were biased against, and overall dwell times were shorter on, old stimuli during search in the preview condition. In addition, the initial onset of search was delayed in the preview condition and saccades made during the preview period did not disrupt the ability to prioritize new items. The data demonstrate directly that preview search results in an attentional bias toward new items and against old items.