Antisaccade costs with static and dynamic targets

In the present study we examined the antisaccade cost (latency difference between antisaccades and prosaccades) in a variety of search tasks. In a series of experiments participants searched for a target and were required to execute a saccade toward (prosaccade) or aw ay (antisaccade) from the target. The results revealed that the antisaccade cost was greater for static targets than for dynamic targets, and it was greater for onset targets than for offset targets. Furthermore, the offset of an onset target interfered with prosaccades, but facilitated antisaccades, resulting in a reduction of the antisaccade cost. To account for the data a model is presented, in which attentional control and working memory processes play an important role in the generation of antisaccades.     

反向眼跳的实验范式、机制及影响因素

反向眼跳任务是研究内源性眼跳的主要方法。1978年,Hallett在研究中首次使用了反向眼跳的实验任务。实验中要求被试抑制对外围目标的注视,并注视它的相反位置。反向眼跳任务是研究行为控制以及注意功能的有效范式。目前认为反向眼跳任务中的朝向眼跳和反向眼跳计划是同时加工并相互竞争的,并且反向眼跳的产生与额顶叶皮层下组织有关。反向眼跳会受到多种因素的影响,例如,空白效应、工作记忆、认知老化、目标离心率等。     

The effect of attentional demands on the antisaccade cost

In the present study, we examined the effect of attentional demands on the antisaccade cost (the latency difference between antisaccades and prosaccades). Participants performed a visual search for a target digit and were required to execute a saccade toward (prosaccade) or away from (antisaccade) the target. The results of Experiment 1 revealed that the antisaccade cost was greater when the target was premasked (i.e., presented through the removal of line segments) than when it appeared as an onset. Furthermore, in premasked target conditions, the antisaccade cost was increased by the presentation of onset distractors. The results of Experiment 2 revealed that the antisaccade cost was greater in a difficult search task (a numeral 2 among 5s) than in an easy one (a 2 among 7s). The findings provide evidence that attentional demands increase the antisaccade cost. We propose that the attentional demands of the search task interfere with the attentional control required to select the antisaccade goal.     

Saccade landing point selection and the competition account of pro- and antisaccade generation: the involvement of visual attention--a review

This paper presents a review and summary of experimental findings on the role of attention in the preparation of saccadic eye movements. The focus is on experiments where performance of prosaccades (saccades towards a suddenly appearing item) and antisaccades (saccades of equal amplitude in the direction opposite to where the target moved) is compared. Evidence suggests that these two opposite responses to the same stimulus event entail competition between neural pathways that generate reflexive movements to the target and neural mechanisms involved in inhibiting the reflex and generating a voluntary gaze shift in the opposite direction to the target appearance. Evidence for such a competition account is discussed in light of a large amount of experimental findings and the overall picture clearly indicates that this competition account has great explanatory power when data on saccadic reaction times and error rates are compared for the two types of saccade. The role of attention is also discussed in particular in light of the finding that the withdrawal of attention by a secondary task 200 to 500 ms before the saccade target appears, leads to speeded antisaccades (without a similar increase in error rates), showing that the results do not simply reflect a speed-accuracy trade-off. This result indicates that the tendency for "reflexive" prosaccades is diminished when attention is engaged in a different task. Furthermore, experiments are discussed that show that as the tendency for a reflexive prosaccade is weakened, antisaccades are speeded up, further supporting the competition account of pro- and antisaccade generation. In the light of evidence from neurophysiology of monkeys and humans, a tentative model of pro- and antisaccade generation is proposed.     

Repetitive antisaccade execution does not increase the unidirectional prosaccade switch-cost

An antisaccade is the execution of a saccade to the mirror-symmetrical location (i.e., same amplitude but opposite visual field) of a single and exogenously presented visual target. Such a response requires top-down decoupling of the normally direct spatial relations between stimulus and response and results in increased planning times and directional errors compared to their spatially compatible prosaccade counterparts. Moreover, antisaccades are associated with diffuse changes in cortical and subcortical saccade networks: a finding that has, in part, been attributed to pre-setting the oculomotor system to withhold a stimulus-driven prosaccade. Moreover, recent work has shown that a corollary cost of oculomotor pre-setting is that the planning time for a to-be-completed prosaccade is longer when preceded by an antisaccade (i.e., the unidirectional prosaccade switch-cost). Notably, this result has been attributed to antisaccades imparting a residual inhibition of the oculomotor networks that support the planning of stimulus-driven prosaccades. In the current investigation, we sought to determine if the number of antisaccades preceding a prosaccade increases this residual inhibition and thus influences the magnitude of the unidirectional prosaccade switch-cost. To that end, participants alternated between pro- and antisaccades after every second (i.e., AABB schedule) and every fourth (i.e., AAAABBBB schedule) trial. In addition, participants completed pro- and antisaccades in separate blocks of trials. Results demonstrated that task-switch prosaccades produced longer reaction times than their task-repetition and blocked condition counterparts, whereas antisaccade reaction times did not vary across task-repetition, task-switch and blocked condition trials. Most notably, the magnitude of the unidirectional prosaccade switch-cost was not modulated across the different task-switching schedules. Thus, we propose that the top-down requirements of the antisaccade task do not produce additive inhibition of stimulus-driven saccade networks.     

The effect of cognitive load on saccadic eye movements

The present study tested the hypothesis that, unlike prosaccades, antisaccades require controlled processing, due to the prepotent response that needs to be inhibited. The effect of the Random time Interval Generation (RIG) task (Vandierendonck, A., De Vooght, G., & Van der Goten, K. (1998). European Journal of Cognitive Psychology, 10, 413-444) on these saccade latencies and errors was studied. This task has the advantage that it loads executive processes, with only minimal interference with verbal or visuo-spatial components. A first experiment compared saccade performance within the prosaccade and the antisaccade task, executed alone and in combination with the RIG task and fixed tapping (added to exclude possible motor component interference explanations). A second experiment investigated the influence of task characteristics on the effects found. Although it was shown that antisaccades are more prone to interference of an executive interference task, it seems that prosaccades are also vulnerable. Interference on prosaccades could originate from a controlled execution of these saccades. A third experiment confirmed that endogenously generated prosaccades are susceptible to dual-task interference and showed that controlled saccade execution, without the need to inhibit a prepotent response, is sufficient to produce interference.     

What is perseverated in schizophrenia? Evidence of abnormal response plasticity in the saccadic system

Although perseveration is sometimes attributed to defective set switching, the authors have recently shown that set-switching is normal in schizophrenia. In this article, the authors tested for persistent states of the saccadic response system, rather than set perseveration. Schizophrenic and healthy subjects performed antisaccades and prosaccades. The authors analyzed for 3 carry-over effects. First, whereas the latency of the current saccade correlated with that of the prior saccade in both groups, the correlations under mixed-task conditions declined in healthy but not in schizophrenic subjects. Second, antisaccades in penultimate trials delayed upcoming saccades in schizophrenic but not in healthy subjects. Third, schizophrenic subjects were more likely to erroneously perseverate the direction of a prior antisaccade but not a prior prosaccade. The authors concluded that, in schizophrenia, the effects of correct antisaccades are persistent not weak. Saccades in schizophrenia are characterized by perseveration of antisaccade-induced changes in the saccadic response system rather than failures to switch task set.     

Are better eye movements an advantage in ball games? A study of prosaccadic and antisaccadic eye movements

The aim of this study was to compare prosaccadic and antisaccadic eye movements of experts in ball sports and controls. In the prosaccadic and antisaccadic task, subjects made saccades respectively towards and away from a suddenly appearing stimulus. By means of infrared-oculography, we compared horizontal eye movements of experts (n=18) and controls (n=20). Experts had shorter overall saccadic latencies, but significantly shorter latencies occurred only on the antisaccade task, not on the prosaccade task. Our findings seem to support the concept that prosaccades and antisaccades have different underlying mechanisms and that expertise in ball games mainly improves antisaccadic performance in terms of latency and variability.     

Attention, spatial integration, and the tail of response time distributions in Stroop task performance

A few studies have examined selective attention in Stroop task performance through ex-Gaussian analyses of response time (RT) distributions. It has remained unclear whether the tail of the RT distribution in vocal responding reflects spatial integration of relevant and irrelevant attributes, as suggested by Spieler, Balota, and Faust (2000). Here, two colour-word Stroop experiments with vocal responding are reported in which the spatial relation between colour and word was manipulated. Participants named colours (e.g., green; say "green") while trying to ignore distractors that were incongruent or congruent words (e.g., red or green), or neutral series of Xs. The vocal RT was measured. Colour words in colour, white words superimposed onto colour rectangles (Experiment 1), and colour rectangles combined with auditory words (Experiment 2) yielded Stroop effects in both the leading edge and the tail of the RT distributions. These results indicate that spatial integration is not necessary for effects in the tail to occur in vocal responding. It is argued that the findings are compatible with an association of the tail effects with task conflict.     

Pro- and antisaccades: dissociating stimulus and response influences the online control of saccade trajectories

The authors examined whether the diminished online control of antisaccades is related to a trade-off between movement planning and control or the remapping of target properties to a mirror-symmetrical location (i.e., vector inversion). Pro- and antisaccades were examined in a standard no-delay schedule wherein target onset served as the movement imperative and a delay cuing schedule wherein responses were initiated 2,000 ms following target onset. Importantly, the delay cuing schedule was employed to equate pro- and antisaccade reaction times. Online control was evaluated by indexing the strength of trajectory amendments at normalized increments of movement time. Antisaccades exhibited fewer online corrections than prosaccades, and this result was consistent across cuing schedules. Thus, the diminished online control of antisaccades cannot be tied to a trade-off between movement planning and control. Rather, the authors propose that the intentional nature of dissociating stimulus and response (i.e., vector inversion) engenders a slow mode of cognitive control that is not optimized for fast oculomotor corrections.     

Pro- and Antisaccades: Dissociating Stimulus and Response Influences the Online Control of Saccade Trajectories

The authors examined whether the diminished online control of antisaccades is related to a trade-off between movement planning and control or the remapping of target properties to a mirror-symmetrical location (i.e., vector inversion). Pro- and antisaccades were examined in a standard no-delay schedule wherein target onset served as the movement imperative and a delay cuing schedule wherein responses were initiated 2,000 ms following target onset. Importantly, the delay cuing schedule was employed to equate pro- and antisaccade reaction times. Online control was evaluated by indexing the strength of trajectory amendments at normalized increments of movement time. Antisaccades exhibited fewer online corrections than prosaccades, and this result was consistent across cuing schedules. Thus, the diminished online control of antisaccades cannot be tied to a trade-off between movement planning and control. Rather, the authors propose that the intentional nature of dissociating stimulus and response (i.e., vector inversion) engenders a slow mode of cognitive control that is not optimized for fast oculomotor corrections.     

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.     

Developmental changes in oculomotor control and working-memory efficiency

In the present study, we examined the developmental changes in the efficiency of saccadic inhibitory control. More specifically, the contribution of age-related changes in working-memory engagement was investigated. We manipulated the efficiency of inhibitory oculomotor control in antisaccade tasks by using fixation-offset conditions, which are supposed to affect inhibitory demands, and by adding increasing working-memory loads to the antisaccade task. In general, in comparison to antisaccade performance of adults, the antisaccade performance of 8-year-old and 12-year-old children was characterized by an increase in direction errors, and/or longer saccadic onset latencies on correct antisaccades. However, this pattern was not altered by the fixation-offset manipulations. In contrast, increased working-memory demands deteriorated 8-year-olds' antisaccade performance unequally as compared to older children and young adults. These findings suggest that - at least in young children - the available functional working-memory capacity is engaged in oculomotor inhibition.     

Cluster analysis reveals distinct patterns of saccade impairment and their relation to cognitive profiles in Parkinson's disease

Saccade performance has been reported to be altered in Parkinson's disease (PD), however, with a large variability between studies as both motor and cognitive impairment interfere with oculomotor control. The aim of this study was to identify different patterns in saccade alterations in PD using a data-driven approach and to explore their relationship with cognitive phenotypes. Sixty-one participants with PD and 25 controls performed eye-tracking (horizontal and vertical prosaccades, antisaccades) and neuropsychological testing. Hierarchical cluster analysis was applied to the eye-tracking data to subsequently compare the clusters based on demographical, clinical and cognitive characteristics. The three identified clusters of saccade alterations differed in cognitive profiles from healthy controls, but not in PD-related motor symptoms or demographics. The rate of directive errors in the antisaccade task was increased in clusters 1 and 2. Further, cluster 1 was defined by a general disinhibition of reflexive saccades and executive dysfunction in the neuropsychological evaluation. In cluster 2, prolonged saccade latencies and hypometria were accompanied by multidomain cognitive impairment. The cluster 3 showed increased antisaccade latency and vertical hypometria despite lack of evidence for cognitive impairment. Our results suggest that there may be at least two opposing patterns of saccade alterations associated with cognitive impairment in PD, which may explain some of the contradictory results of previous studies.     

竞赛特质焦虑干扰抑制功能:对注意控制理论的检验

基于注意控制理论,采用反向眼跳范式,邀请48名运动员参加2项实验,考察竞赛特质焦虑对抑制功能的干扰效应。实验1(25人)为单因素组间设计,探讨竞赛特质焦虑对加工效能和操作成绩的影响。结果发现,竞赛特质焦虑提高眼跳方向错误率,不影响眼跳潜伏期,部分支持竞赛特质焦虑降低加工效能的假设;竞赛特质焦虑不影响按键准确率,支持竞赛特质焦虑不影响操作成绩的假设。实验2(23人)为两因素混合设计,在压力情境下探讨竞赛特质焦虑对加工效能和操作成绩的影响。结果发现,无论是在压力还是非压力情境下,竞赛特质焦虑均提高眼跳方向错误率,延长眼跳潜伏期,但不影响按键准确率,支持压力下竞赛特质焦虑降低加工效能而对操作成绩影响效果不明显的假设。综合2项实验,竞赛特质焦虑干扰抑制功能表现为降低抑制功能的加工效能但对操作成绩的影响效果不明显。本研究提示,注意控制理论适用于解释竞技运动领域焦虑与操作表现的关系。     

Sources of individual differences in the speed of naming objects and actions: The contribution of executive control

We examined the contribution of executive control to individual differences in response time (RT) for naming objects and actions. Following Miyake et al., executive control was assumed to include updating, shifting, and inhibiting abilities, which were assessed using operation span, task-switching, and stop-signal tasks, respectively. Experiment 1 showed that updating ability was significantly correlated with the mean RT of action naming, but not of object naming. This finding was replicated in Experiment 2 using a larger stimulus set. Inhibiting ability was significantly correlated with the mean RT of both action and object naming, whereas shifting ability was not correlated with the mean naming RTs. Ex-Gaussian analyses of the RT distributions revealed that updating ability was correlated with the distribution tail of both action and object naming, whereas inhibiting ability was correlated with the leading edge of the distribution for action naming and the tail for object naming. Shifting ability provided no independent contribution. These results indicate that the executive control abilities of updating and inhibiting contribute to the speed of naming objects and actions, although there are differences in the way and extent these abilities are involved.     

Sources of individual differences in the speed of naming objects and actions: The contribution of executive control

We examined the contribution of executive control to individual differences in response time (RT) for naming objects and actions. Following Miyake et al., executive control was assumed to include updating, shifting, and inhibiting abilities, which were assessed using operation span, task-switching, and stop-signal tasks, respectively. Experiment 1 showed that updating ability was significantly correlated with the mean RT of action naming, but not of object naming. This finding was replicated in Experiment 2 using a larger stimulus set. Inhibiting ability was significantly correlated with the mean RT of both action and object naming, whereas shifting ability was not correlated with the mean naming RTs. Ex-Gaussian analyses of the RT distributions revealed that updating ability was correlated with the distribution tail of both action and object naming, whereas inhibiting ability was correlated with the leading edge of the distribution for action naming and the tail for object naming. Shifting ability provided no independent contribution. These results indicate that the executive control abilities of updating and inhibiting contribute to the speed of naming objects and actions, although there are differences in the way and extent these abilities are involved.     

Changes in same-different laterality patterns as a function of practice and stimulus quality

Accuracy and reaction time (RT) of judgments about sameness vs. difference of (a) names of two letters and (b) shapes of two nonverbal forms were examined for stimuli presented to the center, left (LVF), and right (RVF) visual fields. For same-name letter pairs during Experiment I, responses were more accurate and faster for LVF than for RVF trials on an initial 90-trial block, but this difference was reversed by a third 90-trial block. The RVF advantage for RT was maintained over Trial Blocks 4 and 5, given during a second session, but had disappeared on Trial Blocks 6 through 9 as RT reached the same asymptotic level for both visual fields. No LVF-RVF differences were obtained at any level of practice for different-name letter pairs or for any of the form pairs. Experiment II replicated the shift from LVF toward RVF advantage that occurred over the first three trial blocks of Experiment I and demonstrated that such a shift does not occur when the letters are perceptually degraded. The results were discussed in terms of differences in cerebral hemisphere specialization for visuospatial vs. abstract stages of letter processing and changes with practice in the relative difficulty of these stages.     

Distinguishing common and task-specific processes in word identification: a matter of some moment?

The same 500 words were presented in 6 different word identification tasks (Experiment 1: lexical decision, semantic categorization, and 3 speeded naming tasks; Experiment 2: delayed naming). Reaction time (RT) distributions were estimated for each task and analyses tested for the effects of word frequency and animacy on various parameters of the RT distribution. Low frequency words yielded more skewed distributions than high frequency words in all tasks except delayed naming. The differential skew was most marked for tasks that required lexical discrimination. The semantic categorization task yielded highly skewed distributions for all words, but the word frequency effect was due to shifts in the location of the RT distributions rather than changes in skew. The results are used to evaluate the relative contributions of a common lexical access process and task-specific processes to performance in lexical discrimination and naming tasks.     

Response inhibition and interference control: Effects of schizophrenia,genetic risk,and schizotypy

The ability to inhibit inappropriate responses and suppress irrelevant information is a core feature of executive control. In this study, we provide a detailed analysis of prepotent response inhibition and interference in patients with schizophrenia. To further test the role of genetic factors and subclinical schizophrenia‐like traits, we additionally studied clinically unaffected, first‐degree relatives of schizophrenia patients and assessed dimensions of schizotypy in both relatives and healthy controls. Inhibition and interference control were assessed using a battery comprising the antisaccade, Stroop, stop signal, go/no‐go, flanker, and Simon tasks. Schizophrenia patients differed from both relatives and controls in making more errors on the antisaccade task and having longer response times on the Stroop task, especially the incongruent condition. Patients also had general, that is, condition independent, increases in reaction times on the go/no‐go and flanker tasks and made more errors on the flanker and Simon tasks, suggesting general performance impairments independent of inhibitory demand. Relatives were characterized by hypometric antisaccade amplitude gain despite normal prosaccades, suggesting a selective deficit in non‐standard sensorimotor transformations. Schizotypy was correlated with inhibitory performance across a number of tasks in both relatives and controls. Generally, these effects were independent of verbal intelligence levels. Overall, the findings point to rather selective impairments of inhibitory control in the schizophrenia spectrum and confirm a previously observed deficit in antisaccade spatial accuracy as an endophenotype of schizophrenia.