Time-course of eye movement-related decrease in vividness and emotionality of unpleasant autobiographical memories

The time-course of changes in vividness and emotionality of unpleasant autobiographical memories associated with making eye movements (eye movement desensitisation and reprocessing, EMDR) was investigated. Participants retrieved unpleasant autobiographical memories and rated their vividness and emotionality prior to and following 96 seconds of making eye movements (EM) or keeping eyes stationary (ES); at 2, 4, 6, and 10 seconds into the intervention; then followed by regular larger intervals throughout the 96-second intervention. Results revealed a significant drop compared to the ES group in emotionality after 74 seconds compared to a significant drop in vividness at only 2 seconds into the intervention. These results support that emotionality becomes reduced only after vividness has dropped. The results are discussed in light of working memory theory and visual imagery theory, following which the regular refreshment of the visual memory needed to maintain it in working memory is interfered with by eye movements that also tax working memory, which affects vividness first.     

‘Random’ saccadic eye movements during verbal-linguistic and visual-imaginal tasks

Previous research has suggested that questions eliciting visual imagery are associated with lower rates of saccadic eye movements as compared to questions eliciting verbal processes. Two experiments reported here examined the roles of external visual stimulation and speech output in this effect. In both experiments, questions designed to elicit verbal-linguistic or visual-imaginal processing, and which required either syntactically complex or simple responses, were administered while eye movements were recorded by electrooculography. In experiment 1, 42 subjects responded while viewing either the interviewer's face or a gray oval on a video monitor. Imaginal questions elicited a lower rate of eye movements than did verbal questions regardless of the display on the monitor. In experiment 2, 17 subjects responded in conditions of light and darkness. Imaginal questions elicited lower rates of eye movements in both light and dark. Neither cognitive mode nor speech output requirements interacted with stimulus conditions in either experiment. The failure of visual conditions to influence the verbal-imaginal difference in eye movement rate is viewed as inconsistent with a visual interference interpretation of the relationship of eye movements to cognitive activity. Alternate interpretations are discussed.     

Calibration of an eye-movement system for use in reading

A method for measuring horizontal eye movements in the msec range is described. Accurate measurement of horizontal eye movement over a linear range of 12° is achieved by processing the image of the eye illuminated with infrared light and with the head position fixed. The system has given very reliable results, and a resolution of 6 min of visual angle can be achieved with a character space of 45 min of arc. We also describe efficient numerical-data processing which allows the precise determination of the absolute position of the eye.     

The relationship between eye movements and spatial attention

Most previous studies of the attentional consequences of making saccadic eye movements have used peripheral stimuli to elicit eye movements. It is argued that in the light of evidence showing automatic “capture” of attention by peripheral stimuli, these experiments do not distinguish between attentional effects due to peripheral stimuli and those due to eye movements. In the present study, spatial attention was manipulated by varying the probability that peripheral probe stimuli would appear in different positions, while saccades were directed by a central arrow, enabling the effects of attention and eye movements to be separated. The results showed that the time to react to a peripheral stimulus could be shortened both by advance knowledge of its likely position and, separately, by preparing to make a saccade to that position. When the saccade was directed away from the most likely position of the probe, the targets for attention and eye movements were on opposite sides of the display. In this condition, the effects of preparing to make a saccade proved to be stronger than the effects of attentional allocation until well after the saccade had finished, suggesting that making a saccade necessarily involves the allocation of attention to the target position. The effects of probe stimuli on saccade latencies were also examined: probe stimuli that appeared before the saccade shortened saccade latencies if they appeared at the saccade target, and lengthened saccade latencies if they appeared on the opposite side of fixation. These facilitatory and inhibitory effects were shown to occur at different stages of saccade preparation and suggest that attention plays an important role in the generation of voluntary eye movements. The results of this study indicate that while it is possible to make attention movements without making corresponding eye movements, it is not possible to make an eye movement (in the absence of peripheral stimulation) without making a corresponding shift in the focus of attention.     

Auditory localization: The importance of eye movements and a textured visual environment

Two experiments were designed to investigate the factors involved in the visual facilitation of auditory localization. In both experiments, adult human Ss pointed to targets in a variety of visual conditions. The results of the first experiment showed that target-directed eye movements were important. In the second experiment, eye localization was assessed, along with pointing localization. Both eye and hand localization of the hidden auditory targets were better when target-directed eye movements were made in a lighted environment than when made in the dark. Data also suggested that Ss have better knowledge of their eye position in the light. Possible mechanisms for the involvement of eye movements were suggested, and the theoretical importance of the results was discussed.     

A method for measuring eye movements using Hall-effect devices

A system for precise recording of eye position and movements in laboratory animals, by means of Hall-effect devices, is described. The system, useful in neurophysiological and neurobehavioral studies, allows the analysis of saccadic eye movements, optokinetic- and vestibular-induced nystagmus, slow tracking movements, eye vergences, and so forth. This small, light-weight, and inexpensive system uses a set of Hall-effect devices and associated electronics to sense variations in the position of high-power magnets fixed in the eye sclera or in scleral contact lenses. The output of the Hall-effect devices is amplified by operational amplifiers, collected through an A/D converter, and analyzed in a PC computer by specific software.     

Eye movements and scene perception.

Research on eye movements and scene perception is reviewed. Following an initial discussion of some basic facts about eye movements and perception, the following topics are discussed: (I) the span of effective vision during scene perception, (2) the role of eye movements in scene perception, (3) integration of information across saccades, (4) scene context, object identification and eye movements, and (5) the control of eye movements. The relationship of eye movements during reading to eye movements during scene perception is considered. A preliminary model of eye movement control in scene perception is described and directions for future research are suggested.     

The effect of abnormal displacement of the retinal image during eye movements

The displacement of the images on the retina that results from a turning of the eye does not lead to an apparent motion of what is seen, It has been generally assumed that this is due to a compensating process which takes eye movement into account and serves to discount those image displacements that result from eye movements, It follows from this view that an abnormal image displacement, that is, an image displacement that is larger or smaller than the causing eye movement would warrant, should lead to an experienced displacement of the target. Abnormal image displacement was produced by placing the eye in the converging or diverging bundle of rays from a point source that form behind a strong positive lens; this arrangement yielded a disc-shaped image, the projection of the pupil onto the retina, which displaced abnormally during eye movements. By changing the position of the eye along the axis of the lens in relation to the crossing point of the bundle, the degree to which the displacement was abnormal could be varied, For various displacement rates ranging from 25% to 120 and 400% of normal, abnormal displacements produced by incidental eye movements remained unnoticed, Only where eye movements were intentional did some of our Ss report shifts of the perceived image. It is suggested that the organism copes with the image displacement resulting from the ever-present incidental eye movements not by compensation but by ignoring them.     

Eye movement research on the propositional structure of short texts

The present paper describes the application of computer-based programs to the evaluation of eye movements during reading of short texts. These programs operate in background, that is, after an experimental session is completed and the raw data are collected on magnetic tape. The first program reduces the raw data into a sequence of fixation locations and durations, eye movements, and eye blinks. A second program utilizes calibration coordinates and line-of-text information to transform the reduced data into a standard grid format. Fixation order, locations, and durations for each line of text read are output with respect to the line of text. The final program summarizes fixation locations, frequencies, and durations with respect to analyses of the texts into levels within a hierarchy of propositions in the text base (Kintsch, 1974).     

The effect of prolonged practice of pursuit eye movement

Prolonged exposure to a reciprocating motion that is tracked by the eyes results in diminished extent of perceived motion. Investigation of this effect showed that it becomes manifest only in perceived motion that is caused by ocular pursuit, but that it is not an eye muscle effect. It may consist in a changed evaluation of eye movements. The results throw some light on the relations between the processes that are caused by different stimuli for motion.     

Visual facilitation of auditory localization in schoolchildren: A signal detection analysis

Warren (1970) has claimed that there are visual facilitation effects on auditory localization in adults but not in children. He suggests that a “visual map” organizes spatial information and that considerable experience of correlated auditory and visual events is necessary before normal spatial perception is developed. In the present experiment, children in Grades 1, 4, and 7 had to identify the position, right or left, of a single tone either blindfolded or with their eyes open. Analysis of the proportion of area under the ROC curve (obtained using reaction times) in the respective conditions showed that Ss were more sensitive to auditory position when vision was available. Reaction time was also generally faster in the light. I argue that the increase in sensitivity in the light represents updating of auditory position memory by voluntary eye movement. In the dark, eye movements are subject to involuntary and unperceived drift, which would introduce noise into the eye control mechanism and hence into auditory spatial memory.     

Perceived movement of the afterimage during eye movements

The question of whether an afterimage viewed in a dark field appears to move during eye movement was studied by comparing recordings of eye movements with recordings of reports of perceived movement. The correlation was found to be quite good even under conditions where the eye movements were spontaneous rather than specifically directed. The results were taken to support the hypothesis that the behavior of the retinal image is “interpreted” by taking into account information concerning what the eyes are doing.     

Threat perception in the chameleon (Chamaeleo chameleon): evidence for lateralized eye use

Chameleons are arboreal lizards with highly independent, large amplitude eye movements. In response to an approaching threat, a chameleon on a vertical pole moves so as to keep itself away from the threat. In so doing, it shifts between monocular and binocular scanning of the threat and of the environment. We analyzed eye movements in the Common chameleon, Chamaeleo chameleon, during avoidance response for lateralization, that is, asymmetry at the functional/behavioral levels. The chameleons were exposed to a threat, approaching horizontally from clockwise or anti-clockwise directions, and that could be viewed monocularly or binocularly. Our results show three broad patterns of eye use, as determined by durations spent viewing the threat and by frequency of eye shifts. Under binocular viewing, two of the patterns were found to be both side dependent, that is, lateralized and role dependent ("leading" or "following"). However, under monocular viewing, no such lateralization was detected. We discuss these findings in light of the situation not uncommon in vertebrates, of independent eye movements and a high degree of optic nerve decussation and that lateralization may well occur in organisms that are regularly exposed to critical stimuli from all spatial directions. We point to the need of further investigating lateralization at fine behavioral levels.     

Operant control of eye movements

In a monitoring situation eye movements were required in order for signals to be presented. Detection of signals was the reinforcement. A multiple schedule of fixed-interval reinforcement, differential reinforcement of low rate, and fixed-ratio reinforcement was established for eye movements. Results demonstrated that an eye movement can act as an operant controlled by its consequences. Operant control of eye movements has important implications for human factor analysts concerned with "attention".     

Eye movements during visual mental imagery

It has long been debated whether eye movements play a functional role in visual mental imagery. A recent paper by Laeng and Teodorescu presents new evidence that eye movements are stored as a spatial index that is used to arrange the component parts correctly when mental images are generated.     

Gesturing during mental problem solving reduces eye movements,especially for individuals with lower visual working memory capacity

Non-communicative hand gestures have been found to benefit problem-solving performance. These gestures seem to compensate for limited internal cognitive capacities, such as visual working memory capacity. Yet, it is not clear how gestures might perform this cognitive function. One hypothesis is that gesturing is a means to spatially index mental simulations, thereby reducing the need for visually projecting the mental simulation onto the visual presentation of the task. If that hypothesis is correct, less eye movements should be made when participants gesture during problem solving than when they do not gesture. We therefore used mobile eye tracking to investigate the effect of co-thought gesturing and visual working memory capacity on eye movements during mental solving of the Tower of Hanoi problem. Results revealed that gesturing indeed reduced the number of eye movements (lower saccade counts), especially for participants with a relatively lower visual working memory capacity. Subsequent problem-solving performance was not affected by having (not) gestured during the mental solving phase. The current findings suggest that our understanding of gestures in problem solving could be improved by taking into account eye movements during gesturing.     

眼睛运动如何与记忆相关？

很久以来,人们一直在致力于研究人的眼动与心理活动之间的关系,从而揭示其间的奥妙。众多研究表明,睡眠时的快速眼动（RapidEyeMovements,REM）及其周期对记忆的形成与巩固有重要作用。在清醒状态下,人的眼动就是为了获得视觉信息,如果涉及记忆任务,这就是编码阶段的具体行动。另外,问题解决过程也有眼动参与。总体看来,眼动和记忆之间是一种双向的关系,适当的眼动训练或许能够提高记忆成绩。     

Stopping eye and hand movements: are the processes independent?

To explore how eye and hand movements are controlled in a stop task, we introduced effector uncertainty by instructing subjects to initiate and occasionally inhibit eye, hand, or eye + hand movements in response to a color-coded foveal or tone-coded auditory stop signal. Regardless of stop signal modality, stop signal reaction time was shorter for eye movements than for hand movements, but notably did not vary with knowledge about which movement to cancel. Most errors on eye + hand stopping trials were combined eye + hand movements. The probability and latency of signal respond eye and hand movements corresponded to predictions of Logan and Cowan's (1984) race model applied to each effector independently.     

Effects of subject-to-experimenter distance and instructions on lateral eye movement

Lateral eye movements and heart rate were recorded as 32 right-handed men answered verbal and spatial questions. Experimenter-to-subject distance (.8 and 1.5 m) and attention demand of instructions were manipulated in a 2 X 2 design. A significant main effect for distance and an interaction of distance by instructions appeared on the direction of eye movements independent of type of question. The greatest number of leftward eye movements occurred at the short distance with instructions demanding higher attention. These findings are consistent with evidence that emotional arousal produces greater right- than left-hemisphere activation.     

Conditional control in visual selection

Attention and eye movements provide a window into the selective processing of visual information. Evidence suggests that selection is influenced by various factors and is not always under the strategic control of the observer. The aims of this tutorial review are to give a brief introduction to eye movements and attention and to outline the conditions that help determine control. Evidence suggests that the ability to establish control depends on the complexity of the display as well as the point in time at which selection occurs. Stimulus-driven selection is more probable in simple displays than in complex natural scenes, but it critically depends on the timing of the response: Salience determines selection only when responses are triggered quickly following display presentation, and plays no role in longer-latency responses. The time course of selection is also important for the relationship between attention and eye movements. Specifically, attention and eye movements appear to act independently when oculomotor selection is quick, whereas attentional processes are able to influence oculomotor control when saccades are triggered only later in time. This relationship may also be modulated by whether the eye movement is controlled in a voluntary or an involuntary manner. To conclude, we present evidence that shows that visual control is limited in flexibility and that the mechanisms of selection are constrained by context and time. The outcome of visual selection changes with the situational context, and knowing the constraints of control is necessary to understanding when and how visual selection is truly controlled by the observer.