停表错觉的机制：注意是否为决定因素

通过两个实验探讨了注意是否影响停表错觉（chronostasis）。实验一要求被试在注视时或眼跳后,估计处于眼跳目标或其附近位置的刺激的持续时间;实验二要求被试在眼跳条件下辨别眼跳目标或其附近位置的刺激,以考查两种位置的注意水平。结果表明,眼跳目标位置的注意水平高于其附近位置,而两种位置均可产生停表错觉,且两者的错觉量近似相等。从而说明注意并不影响停表错觉,停表错觉的机制可能是眼跳目标及其附近刺激的知觉提前。     

Top-down control in time and space: Evidence from saccadic latencies and trajectories

Visual distractors disrupt the production of saccadic eye movements temporally, by increasing saccade latency, and spatially, by biasing the trajectory of the movement. The present research investigated the extent to which top-down control can be exerted over these two forms of oculomotor capture. In two experiments, people were instructed to make target directed saccades in the presence of distractors, and temporal and spatial capture were assessed simultaneously by measuring saccade latency and saccade trajectory curvature, respectively. In Experiment 1, an attentional control set manipulation was employed, resulting in the elimination of temporal capture, but only an attenuation of spatial capture. In Experiment 2, foreknowledge of the target location caused an attenuation of temporal capture but an enhancement of spatial capture. These results suggest that, whereas temporal capture is contingent on top-down control, the spatial component of capture is stimulus-driven.     

How longer saccade latencies lead to a competition for salience

It has been suggested that independent bottom-up and top-down processes govern saccadic selection. However, recent findings are hard to explain in such terms. We hypothesized that differences in visual-processing time can explain these findings, and we tested this using search displays containing two deviating elements, one requiring a short processing time and one requiring a long processing time. Following short saccade latencies, the deviation requiring less processing time was selected most frequently. This bias disappeared following long saccade latencies. Our results suggest that an element that attracts eye movements following short saccade latencies does so because it is the only element processed at that time. The temporal constraints of processing visual information therefore seem to be a determining factor in saccadic selection. Thus, relative saliency is a time-dependent phenomenon.     

Latency and accuracy characteristics of saccades and corrective saccades in children and adults

Accuracy and latency characteristics of the first saccade to a target together with the frequency and latency of corrective saccades were studied in children (mean age = 8.5) and adults. The independent variables manipulated were fixation-light offset to target-light onset warning interval (0 and 300 msec) and the presence and location of nontarget stimuli. Although saccade accuracy was significantly affected by nontarget lights, children could respond as accurately as adults and, in replication of previous findings, as quickly when a 300 msec warning interval was given. No speed-accuracy trade off was found for either group as a function of the warning signal condition. Children were as likely to make corrective saccades as adults, but did so with a significantly longer latency. Corrective saccade latencies were greater when a change in direction was required but this effect did not interact with age.     

The influence of saccade length on the saccadic suppression of displacement detection

The decrease in sensitivity to spatial displacement which accompanies a voluntary horizontal saccadic eye movement was measured as a function of the length of the saccade. Threshold for detecting the displacement increased linearly from about 0.3 degrees to 1.2 degrees as saccade length increased from 4 degrees to 12 degrees. The variability (standard deviation) of the discrimination increased linearly with saccade length as well, and hence also linearly with the displacement threshold. These results, along with our previous finding that the increase is not a consequence of the saccadically generated spatiotemporal smearing of the retinal image (Li & Matin, 1990), support the proposal that displacement detection is based on a constant internal signal/noise ratio whose denominator is a measure of the variability of the extraretinal signal regarding eye position, and that the reduction in sensitivity is a result of a transient increase of this variability in the temporal neighborhood of a saccade.     

Saccadic eye movements and dual-task interference

Four dual-task experiments required a speeded manual choice response to a tone in a close temporal proximity to a saccadic eye movement task. In Experiment 1, subjects made a saccade towards a single transient; in Experiment 2, a red and a green colour patch were presented to left and right, and the saccade was to which ever patch was the pre-specified target colour. There was some slowing of the eye movement, but neither task combination showed typical dual-task interference (the “psychological refractory effect”). However, more interference was observed when the direction of the saccade depended on whether a central colour patch was red or green, or when the saccade was directed towards the numerically higher of two large digits presented to the left and the right. Experiment 5 examined a vocal second task, for comparison. The findings might reflect the fact that eye movements can be directed by two separate brain systems--the superior colliculus and the frontal eye fields; commands from the latter but not the former may be delayed by simultaneous unrelated sensorimotor tasks.     

Saccade preparation inhibits reorienting to recently attended locations

We measured manual reaction time in normal human subjects to confirm that an eccentric visual signal has a biphasic effect on covert attention and eye movements. First, it summons attention and biases a saccade toward the signal; a subsequent inhibition of return then slows responses to signals at that location. A temporal hemifield dominance for inhibition of return was shown; this finding converges with observations in neurologic patients to suggest that it is mediated by midbrain pathways. Endogenous orienting of attention, from a central arrow cue, did not activate inhibition of return, whereas endogenous saccade preparation did so as effectively as an exogenous signal, even when no saccade was made. Inhibition of return is activated by midbrain oculomotor pathways and may function as a location "tagging" mechanism to optimize efficiency of visual search.     

Sampling frequency and the study of eye-hand coordination in aiming

This study synchronized sampling of point of gaze (PG) and hand movements in a fast aiming task, using a 60- and a 120-Hz sampling frequency. The subjects moved eyes, head, hand, and trunk freely. For limb kinematics, a significant difference between sampling conditions was only found for the number of accelerations in the profile following peak velocity of the hand. For PG movements, no differences were found for initiation time, saccade angle, fixation duration, and overall number of saccades. However, significant differences were observed for saccade duration. Previously, an invariant feature was found for the ratio of PG and hand response times (50%). For both sampling frequencies, a significant correlation and, thus, temporal coupling was found between PG response time and time to peak acceleration for the hand. Depending on the measures required, a 60-Hz sampling of PG and hand movements may provide as meaningful results as a 120-Hz sampling.     

Task-irrelevant emotional faces impair response adjustments in a double-step saccade task

Cognitive control enables us to adjust behaviours according to task demands, and emotion influences the cognitive control. We examined how task-irrelevant emotional stimuli impact the ability to inhibit a prepared response and then programme another appropriate response. In the study, either a single target or two sequential targets appeared after emotional face images (positive, neutral, and negative). Subjects were required to freely viewed the emotional faces and make a saccade quickly upon target onset, but inhibit their initial saccades and redirect gaze to the second target if it appeared. We found that subjects were less successful at inhibiting their initial saccades as the inter-target delay increased. Emotional faces further reduced their inhibition ability with a longer delay, but not with a shorter delay. When subjects failed to inhibit the initial saccade, the longer delay produced longer intersaccadic interval. Especially, positive faces lengthened the intersaccadic interval with a longer delay. These results showed mere presence of emotional stimuli influences gaze redirection by impairing the ability to cancel a prepared saccade and delaying the programming of a corrective saccade. Therefore, we propose that the modulation of response adjustment exerted by emotional faces is related to the stage of initial response programming.     

Crossmodal action selection: Evidence from dual-task compatibility

Response-related mechanisms of multitasking were studied by analyzing simultaneous processing of responses in different modalities (i.e., crossmodal action). Participants responded to a single auditory stimulus with a saccade, a manual response (single-task conditions), or both (dual-task condition). We used a spatially incompatible stimulus-response mapping for one task, but not for the other. Critically, inverting these mappings varied temporal task overlap in dual-task conditions while keeping spatial incompatibility across responses constant. Unlike previous paradigms, temporal task overlap was manipulated without utilizing sequential stimulus presentation, which might induce strategic serial processing. The results revealed dual-task costs, but these were not affected by an increase of temporal task overlap. This finding is evidence for parallel response selection in multitasking. We propose that crossmodal action is processed by a central mapping-selection mechanism in working memory and that the dual-task costs are mainly caused by mapping-related crosstalk.     

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.     

Remapping versus short-term memory in visual stability across saccades

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

ICAT: a computational model for the adaptive control of fixation durations

Eye movements depend on cognitive processes related to visual information processing. Much has been learned about the spatial selection of fixation locations, while the principles governing the temporal control (fixation durations) are less clear. Here, we review current theories for the control of fixation durations in tasks like visual search, scanning, scene perception, and reading and propose a new model for the control of fixation durations. We distinguish two local principles from one global principle of control. First, an autonomous saccade timer initiates saccades after random time intervals (local-I). Second, foveal inhibition permits immediate prolongation of fixation durations by ongoing processing (local-II). Third, saccade timing is adaptive, so that the mean timer value depends on task requirements and fixation history (Global). We demonstrate by numerical simulations that our model qualitatively reproduces patterns of mean fixation durations and fixation duration distributions observed in typical experiments. When combined with assumptions of saccade target selection and oculomotor control, the model accounts for both temporal and spatial aspects of eye movement control in two versions of a visual search task. We conclude that the model provides a promising framework for the control of fixation durations in saccadic tasks.     

Spatial and temporal factors determine auditory-visual interactions in human saccadic eye movements

In this paper, we show that human saccadic eye movements toward a visual target are generated with a reduced latency when this target is spatially and temporally aligned with an irrelevant auditory nontarget. This effect gradually disappears if the temporal and/or spatial alignment of the visual and auditory stimuli are changed. When subjects are able to accurately localize the auditory stimulus in two dimensions, the spatial dependence of the reduction in latency depends on the actual radial distance between the auditory and the visual stimulus. If, however, only the azimuth of the sound source can be determined by the subjects, the horizontal target separation determines the strength of the interaction. Neither saccade accuracy nor saccade kinematics were affected in these paradigms. We propose that, in addition to an aspecific warning signal, the reduction of saccadic latency is due to interactions that take place at a multimodal stage of saccade programming, where theperceived positions of visual and auditory stimuli are represented in a common frame of reference. This hypothesis is in agreement with our finding that the saccades often are initially directed to the average position of the visual and the auditory target, provided that their spatial separation is not too large. Striking similarities with electrophysiological findings on multisensory interactions in the deep layers of the midbrain superior colliculus are discussed.     

Action, arousal, and subjective time

Saccadic chronostasis refers to the subjective temporal lengthening of the first visual stimulus perceived after an eye movement. It has been quantified using a duration discrimination task. Most models of human duration discrimination hypothesise an internal clock. These models could explain chronostasis as a transient increase in internal clock speed due to arousal following a saccade, leading to temporal overestimation. Two experiments are described which addressed this hypothesis by parametrically varying the duration of the stimuli that are being judged. Changes in internal clock speed predict chronostasis effects proportional to stimulus duration. No evidence for proportionality was found. Two further experiments assessed the appropriateness of the control conditions employed. Results indicated that the chronostasis effect is constant across a wide range of stimulus durations and does not reflect the pattern of visual stimulation experienced during a saccade, suggesting that arousal is not critical. Instead, alternative processes, such as one affecting the onset of timing (i.e., the time of internal clock switch closure) are implicated. Further research is required to select between these alternatives.     

Investigating behavior inhibition in obsessive-compulsive disorder: Evidence from eye movements

We investigated the role of inhibition failure in Obsessive Compulsive Disorder (OCD) through an eye tracking experiment. Twenty-five subjects with OCD were recruited, as well as 25 with Generalized Anxiety Disorder (GAD) and 25 healthy controls. A 3 (group: OCD group, GAD group and control group) × 2 (target eccentricity: far and near) × 2 (saccade task: prosaccade and antisaccade) mixed design was used, with all participants completing two sets of tasks involving both prosaccade (eye movement towards a target) and antisaccade (eye movement away from a target). The main outcome was the eye movement index, including the saccade latency (the time interval from the onset of the target screen to the first saccade) and the error rate of saccade direction. The antisaccade latency and antisaccade error rates for OCDs were much higher than those for GADs and healthy controls. OCDs had longer latency and error rates for antisaccades than for prosaccades, and for far-eccentricity rather than near-eccentricity stimuli. These results suggest that OCDs experience difficulty with behavior inhibition, and that they have higher visual sensitivity to peripheral stimuli. In particular, they show greatest difficulty in inhibiting behavior directed towards peripheral stimuli.     

Oculomotor inhibition of return in normal and mindless reading

Oculomotor inhibition of return (O-IOR) is an increase in saccade latency prior to an eye movement to a recently fixated location, as compared with other locations. To investigate O-IOR in reading, subjects participated in two conditions while their eye movements were recorded: normal reading and mindless reading with words replaced by geometric shapes. We investigated the manifestation of O-IOR in reading and whether it is related to extracting meaning from the text or is an oculomotor phenomenon. The results indicated that fixation durations prior to a saccade returning to the immediately preceding fixated word were longer than those to other words, consistent with O-IOR. Furthermore, fixation durations were longest prior to a saccade that returned the eyes to the specific character position in the word that had previously been fixated and dropped off as the distance between the previously fixated character and landing position increased. This result is consistent with the hypothesis that O-IOR is relatively precise in its application during reading and drops off as a gradient. Both of these results were found for text reading and for mindless reading, suggesting that they are consequences of oculomotor control, and not of language processing. Finally, although these temporal IOR effects were robust, no spatial consequences of IOR were observed: Previously fixated words and characters were as likely to be refixated as new words and characters.     

The control of saccade trajectories: direction of curvature depends on prior knowledge of target location and saccade latency

Recent reports have shown that saccades can deviate either toward or away from distractors. However, the specific conditions responsible for the change in initial saccade direction are not known. One possibility, examined here, is that the direction of curvature (toward or away from distractors) reflects preparatory tuning of the oculomotor system when the location of the target and distractor are known in advance. This was investigated by examining saccade trajectories under predictable and unpredictable target conditions. In Experiment 1, the targets and the distractors appeared unpredictably, whereas in Experiment 2 an arrow cue presented at fixation indicated the location of the forthcoming target prior to stimulus onset. Saccades were made to targets on the horizontal, vertical, and principal oblique axis, and distractors appeared simultaneously at an adjacent location (a separation of +/- 45 degrees of visual angle). On average, saccade trajectories curved toward distractors when target locations were unpredictable and curved away from distractors when target locations were known in advance. There was no overall difference in mean saccade latencies between the two experiments. The magnitude of the distractor modulation of saccade trajectory (either toward or away from) was comparable across the different saccade directions (horizontal, vertical, and oblique). These results are interpreted in terms of the time course of competitive interactions operating in the neural structures involved in the suppression of distractors and the selection of a saccade target. A relatively slow mechanism that inhibits movements to distractors produces curvature away from the distractor. This mechanism has more time to operate when target location is predictable, increasing the likelihood that the saccade trajectory will deviate away from the distractor.     

Neurophysiology and neuroanatomy of reflexive and volitional saccades: Evidence from studies of humans

This review provides a summary of the contributions made by human functional neuroimaging studies to the understanding of neural correlates of saccadic control. The generation of simple visually guided saccades (redirections of gaze to a visual stimulus or pro-saccades) and more complex volitional saccades require similar basic neural circuitry with additional neural regions supporting requisite higher level processes. The saccadic system has been studied extensively in non-human (e.g., single-unit recordings) and human (e.g., lesions and neuroimaging) primates. Considerable knowledge of this system’s functional neuroanatomy makes it useful for investigating models of cognitive control. The network involved in pro-saccade generation (by definition largely exogenously-driven) includes subcortical (striatum, thalamus, superior colliculus, and cerebellar vermis) and cortical (primary visual, extrastriate, and parietal cortices, and frontal and supplementary eye fields) structures. Activation in these regions is also observed during endogenously-driven voluntary saccades (e.g., anti-saccades, ocular motor delayed response or memory saccades, predictive tracking tasks and anticipatory saccades, and saccade sequencing), all of which require complex cognitive processes like inhibition and working memory. These additional requirements are supported by changes in neural activity in basic saccade circuitry and by recruitment of additional neural regions (such as prefrontal and anterior cingulate cortices). Activity in visual cortex is modulated as a function of task demands and may predict the type of saccade to be generated, perhaps via top-down control mechanisms. Neuroimaging studies suggest two foci of activation within FEF - medial and lateral - which may correspond to volitional and reflexive demands, respectively. Future research on saccade control could usefully (i) delineate important anatomical subdivisions that underlie functional differences, (ii) evaluate functional connectivity of anatomical regions supporting saccade generation using methods such as ICA and structural equation modeling, (iii) investigate how context affects behavior and brain activity, and (iv) use multi-modal neuroimaging to maximize spatial and temporal resolution.     

Neurophysiology and neuroanatomy of reflexive and volitional saccades: evidence from studies of humans

This review provides a summary of the contributions made by human functional neuroimaging studies to the understanding of neural correlates of saccadic control. The generation of simple visually guided saccades (redirections of gaze to a visual stimulus or pro-saccades) and more complex volitional saccades require similar basic neural circuitry with additional neural regions supporting requisite higher level processes. The saccadic system has been studied extensively in non-human (e.g., single-unit recordings) and human (e.g., lesions and neuroimaging) primates. Considerable knowledge of this system’s functional neuroanatomy makes it useful for investigating models of cognitive control. The network involved in pro-saccade generation (by definition largely exogenously-driven) includes subcortical (striatum, thalamus, superior colliculus, and cerebellar vermis) and cortical (primary visual, extrastriate, and parietal cortices, and frontal and supplementary eye fields) structures. Activation in these regions is also observed during endogenously-driven voluntary saccades (e.g., anti-saccades, ocular motor delayed response or memory saccades, predictive tracking tasks and anticipatory saccades, and saccade sequencing), all of which require complex cognitive processes like inhibition and working memory. These additional requirements are supported by changes in neural activity in basic saccade circuitry and by recruitment of additional neural regions (such as prefrontal and anterior cingulate cortices). Activity in visual cortex is modulated as a function of task demands and may predict the type of saccade to be generated, perhaps via top-down control mechanisms. Neuroimaging studies suggest two foci of activation within FEF - medial and lateral - which may correspond to volitional and reflexive demands, respectively. Future research on saccade control could usefully (i) delineate important anatomical subdivisions that underlie functional differences, (ii) evaluate functional connectivity of anatomical regions supporting saccade generation using methods such as ICA and structural equation modeling, (iii) investigate how context affects behavior and brain activity, and (iv) use multi-modal neuroimaging to maximize spatial and temporal resolution.