Attentional capture and aging: implications for visual search performance and oculomotor control

Two studies examined potential age-related differences in attentional capture. Subjects were instructed to move their eyes as quickly as possible to a color singleton target and to identify a small letter located inside it. On half the trials, a new stimulus (i.e., a sudden onset) appeared simultaneously with the presentation of the color singleton target. The onset was always a task-irrelevant distractor. Response times were lengthened, for both young and old adults, whenever an onset distractor appeared, despite the fact that subjects reported being unaware of the appearance of the abrupt onset. Eye scan strategies were also disrupted by the appearance of the onset distractors. On about 40% of the trials on which an onset appeared, subjects made an eye movement to the task-irrelevant onset before moving their eyes to the target. Fixations close to the onset were brief, suggesting parallel programming of a reflexive eye movement to the onset and goal-directed eye movement to the target. Results are discussed in terms of age-related sparing of the attentional and oculomotor processes that underlie attentional capture.     

The role of stimulus-driven and goal-driven control in saccadic visual selection

Four experiments were conducted to investigate the role of stimulus-driven control in saccadic eye movements. Participants were required to make a speeded saccade toward a predefined target presented concurrently with multiple nontargets and possibly 1 distractor. Target and distractor were either equally salient (Experiments 1 and 2) or not (Experiments 3 and 4). The results uniformly demonstrated that fast eye movements were completely stimulus driven, whereas slower eye movements were goal driven. These results are in line with neither a bottom-up account nor a top-down notion of visual selection. Instead, they indicate that visual selection is the outcome of 2 independent processes, one stimulus driven and the other goal driven, operating in different time windows.     

Speed and accuracy of saccadic eye movements: characteristics of impulse variability in the oculomotor system

Dynamic characteristics observed in the trajectories of saccadic eye movements reveal systematic variability of the force pulses used to move the eyes. This variability causes saccades to exhibit a linear speed-accuracy trade-off: As the average distance and duration of saccades toward specified target points increase, the standard deviations of saccadic-movement endpoints increase linearly with the saccades' average velocity. The linear trade-off, and other observed stochastic properties of saccades, may be attributed to noise in neuromotor processes and may be described in terms of an impulse-variability model originally designed for characterizing limb movements. According to the model, both eye and limb movements are controlled through stochastic force and time parameters that govern movement kinematics. Such an account may promote a unified conceptual framework for understanding a wide range of motor behavior.     

Evidence for visual persistence during saccadic eye movements

Summary 1. The persistence of visual perception was investigated under conditions of visual fixation as well as eye movement. The Ss' task was to discriminate brief double light impulses; their responses were recorded as a function of the duration of the interstimulus interval. Based on these data the critical interstimulus interval was calculated, which yielded equal response frequencies for the perception of one or two stimuli upon presentation of double light pulses.2. In the condition of visual fixation the two stimuli could not be discriminated until the mean value of interstimulus interval exceeded 73 msec. In the condition with eye movements, when the first stimulus was presented in the parafoveal region of the retina before the beginning of the saccade and the second stimulus in the foveal region just after termination of the eye movement, this duration was shown to be statistically of the same magnitude (76 msec).3. Possible alternative interpretations of this latter result, e.g., that it could be explained in terms of masking or saccadic suppression rather than visual persistence was discussed; it was attempted to invalidate such explanations by means of three control experiments.4. The main result, the persistence of visual perception during voluntary eye movements, was discussed in relation to the problem of spatial and temporal stability of visual perception.I thank Prof. Dr. H.W. Wendt for support in correcting the English translation.     

Saccades to targets in three-dimensional space: Dependence of saccadic latency on target location

The latency of saccadic movements to targets appearing at various positions in three-dimensional visual space was measured in four experiments. The first experiment confirmed that latencies of saccades to visual targets are greater in the lower visual field and showed that the increase is not influenced by the vertical starting position of the eye in the orbit, nor by a time gap between the fixation offset and the target onset. A hypothesis that this visual field difference was caused by a link between downward saccades and convergence movements was tested by recording saccade latencies when the targets were in a different depth plane from that of the original fixation. We did not find any direct support for the vergence involvement hypothesis, although the lower/upper visual field effect was shown to decrease consistently in monocular viewing. It was also shown that saccades to targets positioned in a different depth plane have longer latencies. In a final experiment, the visual field effect was shown to depend on the egocentric rather than the gravitational vertical.     

Visual and oculomotor selection: links, causes and implications for spatial attention

Natural scenes contain far more information than can be processed simultaneously. Thus, our visually guided behavior depends crucially on the capacity to attend to relevant stimuli. Past studies have provided compelling evidence of functional overlap of the neural mechanisms that control spatial attention and saccadic eye movements. Recent neurophysiological work demonstrates that the neural circuits involved in the preparation of saccades also play a causal role in directing covert spatial attention. At the same time, other studies have identified separable neural populations that contribute uniquely to visual and oculomotor selection. Taken together, all of the recent work suggests how visual and oculomotor signals are integrated to simultaneously select the visual attributes of targets and the saccades needed to fixate them.     

The spatial signal for saccadic eye movements emphasizes visual boundaries

By investigating the visual processing involved when saccades are made to newly appearing targets, we show that this processing is significantly nonlinear and that texture boundary information predominates. We used the global, or center-of-gravity, effect whereby a saccadic eye movement directed to a target consisting of a pair of elements has an amplitude intermediate between that of saccades directed to the individual elements. We measured the effect using target elements with different visual characteristics, including phase-reversal checkerboard targets that had the same space-average luminance as the background. The contribution to the center-of-gravity calculation was used to measure relative salience. We found that positive and negative contrast elements contribute almost equal weightings. Thus, salience, assessed in this way, is a highly nonlinear function of luminance. The salience of checkerboard targets was found to decrease as check size was decreased and increase as the overall size of the target was increased. Checkerboards with an empty center were as effective as were full checkerboards, showing the importance of boundaries in the salience signal.     

Development of attentional and oculomotor control

The present study was conducted to examine the development of attentional and oculomotor control. More specifically, the authors were interested in the development of the ability to inhibit an incorrect but prepotent response to a salient distractor. Participants, who ranged in age from 8 to 25 years, performed 3 different eye movement tasks: a prosaccade, an antisaccade, and an oculomotor capture task. The time required to initiate a saccade decreased with age across all 3 tasks. Consistent with previous reports, accuracy was relatively age invariant in the prosaccade task. Performance improved with age, asymptoting at 16 years in the antisaccade task. It is interesting to note that despite the superficial similarity of the antisaccade and oculomotor capture tasks, performance was relatively age invariant in the latter. These results are discussed in terms of developmental differences in the interaction of goal-directed and stimulus-driven processes in the control of attention and action.     

Saccades to targets in three-dimensional space: dependence of saccadic latency on target location.

The latency of saccadic movements to targets appearing at various positions in three-dimensional visual space was measured in four experiments. The first experiment confirmed that latencies of saccades to visual targets are greater in the lower visual field and showed that the increase is not influenced by the vertical starting position of the eye in the orbit, nor by a time gap between the fixation offset and the target onset. A hypothesis that this visual field difference was caused by a link between downward saccades and convergence movements was tested by recording saccade latencies when the targets were in a different depth plane from that of the original fixation. We did not find any direct support for the vergence involvement hypothesis, although the lower/upper visual field effect was shown to decrease consistently in monocular viewing. It was also shown that saccades to targets positioned in a different depth plane have longer latencies. In a final experiment, the visual field effect was shown to depend on the egocentric rather than the gravitational vertical.     

Mapping the color space of saccadic selectivity in visual search

Color coding is used to guide attention in computer displays for such critical tasks as baggage screening or air traffic control. It has been shown that a display object attracts more attention if its color is more similar to the color for which one is searching. However, what does similar precisely mean? Can we predict the amount of attention that a display color will receive during a search for a given target color? To tackle this question, two color‐search experiments measuring the selectivity of saccadic eye movements and mapping out its underlying color space were conducted. A variety of mathematical models, predicting saccadic selectivity for given target and display colors, were devised and evaluated. The results suggest that applying a Gaussian function to a weighted Euclidean distance in a slightly modified HSI color space is the best predictor of saccadic selectivity in the chosen paradigm. Hue and intensity information by itself provides a basis for useful predictors, spanning a possibly spherical color space of saccadic selectivity. Although the current models cannot predict saccadic selectivity values for a wide variety of visual search tasks, they reveal some characteristics of color search that are of both theoretical and applied interest, such as for the design of human–computer interfaces.     

Quantification and analysis of saccadic and smooth pursuit eye movements and fixations to detect oculomotor deficits

Assessment of deficits in oculomotor function may be useful to detect visuomotor impairments due to a closed head injury. Systematic analysis schemes are needed to reliably quantify oculomotor deficits associated with oculomotor impairment via brain trauma. We propose a systematic, automated analysis scheme using various eye-tracking tasks to assess oculomotor function in a cohort of adolescents with acute concussion symptoms and aged-matched healthy controls. From these data we have evidence that these methods reliably detect oculomotor deficits in the concussed group, including reduced spatial accuracy and diminished tracking performance during visually guided prosaccade and self-paced saccade tasks. The accuracy and tracking deficits are consistent with prior studies on oculomotor function, while introducing novel discriminatory measures relative to fixation assessments – methodologically, a less complicated measure of performance – and thus represent a reliable and simple scheme of detection and analysis of oculomotor deficits associated with brain injury.     

Response latency in visual search with redundancy in the visual display

Two experiments were run to investigate the effects of redundant display items upon response latency in a visual search task. In the first study, Ss searched five-letter displays for a predesignated critical letter. Both critical and noncritical letters could be repeated in the displays. Mean response latency decreased markedly with increasing redundancy in the critical letter and was affected to a lesser extent by redundancy in the noncritical letters. In the second study, Ss were required to detect the presence of redundant letters in displays of from two to five letters, first with no information as to what letter might be repeated, then with knowledge of which letter would be repeated if the display contained a redundant letter. Response latencies in the former case were much slower than in the latter. The implications of these findings for current views of visual information processing were discussed.     

Spatial distribution of visual attention: Perceptual sensitivity and response latency

Studies of the spatial distribution of visual attention have shown that attentional facilitation monotonically decreases in a graded fashion with increasing distance from an attended location. However, reaction time (RT) measures have typically shown broader gradients than have signal detection (SD) measures of perceptual sensitivity. It is not clear whether these differences have arisen because the stages of information processing indexed by RT measures are different from those indexed by SD measures, or whether these differences are due to methodological confounds in the SD studies. In the present set of experiments, the spatial distribution of attention was studied by using a luminance detection task in an endogenous cuing paradigm that was designed to permit accurate calculations of SD and RT measures for targets at cued and uncued locations. Subjects made target-present/absent decisions at one of six possible cued or uncued upper visual hemifield locations on each trial. The results from three experiments suggest that the differences between broad and focal attentional distributions are not the result of different stages of information processing indexed by RT measures as opposed to SD measures. Rather, the differing distributions appear to reflect variations in attentional allocation strategies induced by the perceptual requirements typical of RT paradigms as opposed to SD paradigms. These findings support numerous prior studies showing that spatial attention affects perceptual sensitivity and that the strategic allocation of attention is a highly flexible process.     

The reduction of saccadic latency by prior offset of the fixation point: an analysis of the gap effect

The latency to initiate a saccade (saccadic reaction time) to an eccentric target is reduced by extinguishing the fixation stimulus prior to the target onset. Various accounts have attributed this latency reduction (referred to as the gap effect) to facilitated sensory processing, oculomotor readiness, or attentional processes. Two experiments were performed to explore the relative contributions of these factors to the gap effect. Experiment 1 demonstrates that the reduction in saccadic reaction time (RT) produced by fixation point offset is additive with the effect of target luminance. Experiment 2 indicates that the gap effect is specific for saccades directed toward a peripheral target and does not influence saccades directed away from the target (i.e., antisaccades) or choice-manual RT. The results are consistent with an interpretation of the gap effect in terms of facilitated premotor processing in the superior colliculus.     

Cognitive control of saccadic eye movements

The saccadic eye movement system provides researchers with a powerful tool with which to explore the cognitive control of behaviour. It is a behavioural system whose limited output can be measured with exceptional precision, and whose input can be controlled and manipulated in subtle ways. A range of cognitive processes (notably those involved in working memory and attention) have been shown to influence saccade parameters. Researchers interested in the relationship between cognitive function and psychiatric disorders have made extensive use of saccadic eye movement tasks to draw inferences as to the cognitive deficits associated with particular psychopathologies. The purpose of this review is to provide researchers with an overview of the research literature documenting cognitive involvement in saccadic tasks in healthy controls. An appreciation of this literature provides a solid background against which to interpret the deficits on saccadic tasks demonstrated in patient populations.     

Area activation: a computational model of saccadic selectivity in visual search

The Area Activation Model (Pomplun, Reingold, Shen, & Williams, 2000) is a computational model predicting the statistical distribution of saccadic endpoints in visual search tasks. Its basic assumption is that saccades in visual search tend to foveate display areas that provide a maximum amount of task‐relevant information for processing during the subsequent fixation. In the present study, a counterintuitive prediction by the model is empirically tested, namely that saccadic selectivity towards stimulus features depends on the spatial arrangement of search items. We find good correspondence between simulated and empirically observed selectivity patterns, providing strong support for the Area Activation Model.     

The role of visual attention in saccadic eye movements

The relationship between saccadic eye movements and covert orienting of visual spatial attention was investigated in two experiments. In the first experiment, subjects were required to make a saccade to a specified location while also detecting a visual target presented just prior to the eye movement. Detection accuracy was highest when the location of the target coincided with the location of the saccade, suggesting that subjects use spatial attention in the programming and/or execution of saccadic eye movements. In the second experiment, subjects were explicitly directed to attend to a particular location and to make a saccade to the same location or to a different one. Superior target detection occurred at the saccade location regardless of attention instructions. This finding shows that subjects cannot move their eyes to one location and attend to a different one. The results of these experiments suggest that visuospatial attention is an important mechanism in generating voluntary saccadic eye movements.     

A generalized visual latency explanation of the Pulfrich phenomenon

The classical visual latency explanation of the Pulfrich phenomenon is generalized to allow for the possibility that the visual system uses velocity information from motion detectors to compensate for spatial lag due to time lag, in identifying the instantaneous position of a moving object. The results of the reported experiment verify one consequence of the generalized version: the elliptical apparent path is skewed away from the filtered eye. The results suggest also that the extrapolation factor increases with visual latency and that there is a different extrapolation factor for each eye when the eyes are illuminated unequally.     

Cognitive control of saccadic eye movements

The saccadic eye movement system provides researchers with a powerful tool with which to explore the cognitive control of behaviour. It is a behavioural system whose limited output can be measured with exceptional precision, and whose input can be controlled and manipulated in subtle ways. A range of cognitive processes (notably those involved in working memory and attention) have been shown to influence saccade parameters. Researchers interested in the relationship between cognitive function and psychiatric disorders have made extensive use of saccadic eye movement tasks to draw inferences as to the cognitive deficits associated with particular psychopathologies. The purpose of this review is to provide researchers with an overview of the research literature documenting cognitive involvement in saccadic tasks in healthy controls. An appreciation of this literature provides a solid background against which to interpret the deficits on saccadic tasks demonstrated in patient populations.