The effects of abrupt onset of 2-D and 3-D distractors on prehension movements

This article includes two experiments aimed at investigating how two-dimensional (2-D) and threedimensional (3-D) distractors affect the kinematics of prehension and aiming movements in order to understand the attentional processes involved in visuomotor control. In Experiment 1, subjects grasped large targets in the presence of both large and small 3-D distractors and their corresponding 2-D photographs. The distractors appeared for either 10 sec or appeared simultaneously with the target presentation. It was found that reach and grasp kinematics were influenced primarily by the small, suddenly appearing 3-D distractors. In Experiment 2, the purpose was to examine the conclusion that competition between objects (target and distractor) is related to the behavioral goal of the task. Experiment 2 is a replication of Experiment 1, with the exception that pointing movements were made instead of grasping movements. Results show that both 3-D and 2-D distractors interfered with pointing kinematics, supporting the hypothesis that attentional mechanisms are related to the goal of the task.     

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.     

Attentional selection during preparation of prehension movements

In two experiments coupling between dorsal attentional selection for action and ventral attentional selection for perception during preparation of prehension movements was examined. In a dual-task paradigm subjects had to grasp an X-shaped object with either the left or the right hand's thumb and index finger. Simultaneously a discrimination task was used to measure visual attention prior to the execution of the prehension movements: Mask items transiently changed into distractors or discrimination targets. There was exactly one discrimination target per trial, which appeared at one of the four branch ends of the object. In Experiment 1 target position varied randomly while in Experiment 2 it was constant and known to subjects in each block of trials. In both experiments discrimination performance was significantly better for discrimination target positions at to-be-grasped branch ends than for not-to-be-grasped branch ends. We conclude that during preparation of prehension movements visual attention is largely confined to those parts of an object that will be grasped.     

A controlled-attention view of working-memory capacity.

In 2 experiments the authors examined whether individual differences in working-memory (WM) capacity are related to attentional control. Experiment 1 tested high- and low-WM-span (high-span and low-span) participants in a prosaccade task, in which a visual cue appeared in the same location as a subsequent to-be-identified target letter, and in an antisaccade task, in which a target appeared opposite the cued location. Span groups identified targets equally well in the prosaccade task, reflecting equivalence in automatic orienting. However, low-span participants were slower and less accurate than high-span participants in the antisaccade task, reflecting differences in attentional control. Experiment 2 measured eye movements across a long antisaccade session. Low-span participants made slower and more erroneous saccades than did high-span participants. In both experiments, low-span participants performed poorly when task switching from antisaccade to prosaccade blocks. The findings support a controlled-attention view of WM capacity.     

Task- and location-switching effects on visual attention

In two experiments, we examined the effects of task and location switching on the accuracy of reporting target characters in an attentional blink (AB) paradigm. Single-character streams were presented at a rate of 100 msec per character in Experiment 1, and successive pairs of characters on either side of fixation were presented in Experiment 2. On each trial, two targets appeared that were either white letters or black digits embedded in a stream of black letter distractors, and they were separated by between zero and five items in the stream (lags 1-6). Experiment 1 showed that report of the first target was least accurate if it immediately preceded the second target and if the two targets were either both letters or both digits (task repetition cost). Report of the second target was least accurate if one or two distractors intervened between the two targets (the U-shaped AB lag effect) and if one target was a letter and the other a digit (task switch cost). Experiment 2 added location uncertainty as a factor and showed similar effects as Experiment 1, with one exception. Lag 1 sparing (the preserved accuracy in reporting the second of two targets if the second immediately follows the first) was completely eliminated when the task required attention switching across locations. Two-way additive effects were found between task switching and location switching in the AB paradigm. These results suggests separate loci for their attentional effects. It is likely that the AB deficit is due mainly to central memory limitations, whereas location-switching costs occur at early visual levels. Task-switching costs occur at an intermediate visual level, since the present task switch involved encoding differences without changes in stimulus-response mapping rules (i.e., the task was character identification for both letters and digits).     

Adaptation to prisms: Do proprioceptive changes mediate adapted behaviour with ballistic arm movements?

In Experiment I subjects pointed repeatedly at a target viewed through laterally displacing prisms and received terminal visual feedback. In one task the pointing movements were slow (proprioceptively controlled), and in the other they were fast (pre-programmed). In both tasks adaptation proceeded at the same rate and to the same level of performance. Following fast pointing with prisms a large amount of arm-body adaptation was found with slow and fast test movements, while following slow pointing with prisms a large amount of arm-body adaptation was found with slow test movements, but only a small amount with fast test movements. The result suggests that adapted behaviour with preprogrammed movements is not mediated by a proprioceptive change. In Experiment II pointing movements were passive. No arm-body adaptation was found with fast test movements, and, contrary to expectation, only a small amount with slow test movements.     

Influence of hand position on the near effect in 3-D attention

Voluntary reorienting of attention in real depth situations is characterized by an attentional bias to locations nearer the viewer once attention is deployed to a spatially cued object in depth. Previously, this effect (initially referred to as the near effect) was attributed to access of a 3-D viewer-centered spatial representation for guiding attention in 3-D space. The aim of this study was to investigate whether the near effect could have been associated with the position of the response hand, which was always near the viewer in previous studies that investigated endogenous attentional shifts in real depth. In Experiment 1, the response hand was placed at either the near or far target depth in a depth-cuing task. Placing the response hand at the far target depth abolished the near effect, but failed to bias spatial attention to the far location. Experiment 2 showed that the response hand effect was not modulated by the presence of an additional (passive) hand, whereas Experiment 3 confirmed that attentional prioritization of the passive hand was not masked by the influence of the responding hand on spatial attention in Experiment 2. The pattern of results is most consistent with the idea that response preparation can modulate spatial attention within a 3-D viewer-centered spatial representation.     

Response times and eye movements in feature and conjunction search as a function of target eccentricity

In four experiments, saccadic eye movements, reaction times (RTs), and accuracy were measured as observers searched for feature or conjunction targets presented at several eccentricities. A conjunction search deficit, evidenced by a large eccentricity effect on RTs, accuracy, and number of saccades, was seen in Experiments 1A and 1B. Experiment 2 indicated that, when saccades were precluded, there was an even larger eccentricity effect for conjunction search targets. In Experiment 3, practice in a conjunction search task allowed both RT and number of saccades to become independent of eccentricity. Additionally, there was evidence of feature-based selectivity in that observers were more likely to fixate distractors that had the same contrast as the target. Results are consistent with the view that the oculomotor and attentional systems are functionally linked and provide constraints for models of visual attention and search.     

Distractor interference in focused attention tasks is not mediated by attention capture

Distractor stimuli possessing information that is relevant for a task (henceforth, task-relevant distractors) often interfere with task performance. The interference by task-relevant distractors is observed even when distractors are positioned outside the main attentional focus. We investigated whether such interference is due to an attention capture by the distractors. Participants responded to a target colour while ignoring word distractors positioned within (Experiment 1) or outside (Experiments 2 and 3) the attentional focus. The words carried task-relevant information in their colour and personally significant information in their content. Because personally significant information affects performance only when positioned in an attended region, it was used as a marker for the locus of the attentional focus. As expected, when distractors were attended, both task-relevant and personally significant information affected performance. However, when distractors were unattended, only task-relevant information caused interference, suggesting that attention did not shift to the distractors’ location. We discuss possible accounts for interference effects in focused-attention tasks.     

Grasping remaps the distribution of visuospatial attention and enhances competing action activation

We examined how action goals influence the distribution of visuospatial attention near the body (Experiment 1) and how the temporal relationship between distractors and targets modifies shifts in visuospatial attention (Experiment 2). Targets were light emitting diodes (LEDs) in the left and right hemispace of a visual display. Following left or right target illumination, participants reached to point-to or grasp target object in blocked trials. Coincident with target onset, a distractor LED illuminated in the same or opposite hemispace between the initiation point and target, or no distractor appeared. In Experiment 1, during grasping there was a larger temporal interference effect (slower reach initiation) than with pointing. When grasping versus pointing, participants deviated more towards same-side distractors and away from opposite-side distractors. In Experiment 2, distractors onset 200ms prior to (?200-ms), coincident with (0 ms), or 200ms following (+200 ms) the target. For both reach types, ?200-ms distractors had greater onset temporal interference than 0 ms and +200-ms distractors. For grasping, +200 ms distractors had larger temporal interference than 0 ms distractors. For ?200-ms, reach trajectories deviated more towards opposite-side distractors and away from same-side distractors, the reverse of the pattern for 0 ms and +200-ms distractors.     

无关工作记忆表征的负性情绪信息能否捕获视觉注意?一项眼动研究

研究通过分析视觉搜索任务的首次注视点和行为反应时, 探讨无关工作记忆表征的负性情绪信息对视觉注意选择的影响。实验1发现在反映早期注意选择的首次注视点百分率指标上, 不管工作记忆表征的情绪效价如何, 均出现了显著的注意捕获效应; 实验2发现当采用中性情绪靶子刺激时, 首次注视点百分率指标上仍表现出了稳健的注意捕获效应; 在首次注视点持续时间指标上, 实验1和实验2均发现记忆匹配条件的干扰刺激显著小于控制条件的干扰刺激, 表现出注意的快速脱离; 而在行为反应时指标上, 早期的注意捕获效应消失(实验1), 甚至被反转为注意抑制效应(实验2)。这些结果表明在早期注意选择阶段, 记忆驱动的注意捕获效应不受工作记忆表征情绪效价的影响, 但认知控制会在早期注意捕获之后促使注意快速脱离记忆匹配的干扰刺激, 其作用效果受靶子刺激情绪效价的调节。     

工作记忆表征精度加工需求对注意引导的影响

采用注意捕获范式, 通过行为和事件相关脑电位(ERP)实验, 探讨工作记忆表征精度加工需求对注意引导的影响, 行为结果发现, 在低精度加工需求条件下, 只有一个工作记忆表征引导注意, 且处于高激活状态的工作记忆表征产生的注意捕获大于低激活状态; 而在高精度加工需求条件下, 有两个工作记忆表征引导注意, 且处于高、低激活状态的工作记忆表征产生的注意捕获没有差异。ERP结果显示, 高精度加工需求条件下诱发的NSW和LPC大于低精度加工需求条件; 在高精度加工需求条件下, 干扰项与记忆项匹配比不匹配时, 诱发更大的N2和更小的N2pc, 而在低精度加工需求条件下, 干扰项与记忆项匹配和不匹配时诱发的N2、N2pc没有差异。研究表明, 工作记忆表征精度加工需求影响注意引导的机制可能是高精度加工需求下, 工作记忆表征消耗的认知资源增加, 搜索目标获得的资源减少, 干扰项捕获的注意增加。     

Target- and effect-directed actions towards temporal goals: Similar mechanisms?

The goal of an action can consist of generating a change in the environment (to produce an effect) or changing one's own situation in the environment (to move to a physical target). To investigate whether the mechanisms of effect-directed and target-directed action control are similar, participants performed continuous reversal movements. They either synchronized movement reversals with regularly presented tones (temporal targets) or produced tones at reversals isochronously (temporal effects). In both goal conditions an irrelevant goal characteristic was integrated into the goal representation (loudness, Experiment 1). When targets and effects were presented within the same reversal movement, similarities were enhanced (Experiment 2). When the task posed spatial demands in addition to temporal demands, target- and effect-directed movement kinematics changed equally with tempo (Experiment 3). Correlations between target-directed and effect-directed movements in temporal variability indicated similar timing mechanisms (Experiments 1 and 2). Only gradual differences between target- and effect-directed movements were observed. We conclude that the same mechanisms of action control, including the anticipation of upcoming events, underlie effect-directed and target-directed movements. Ideomotor theories of action control should incorporate action targets as goals similar to action effects. (PsycINFO Database Record (c) 2012 APA, all rights reserved).     

The adaptive character of the attentional system: statistical sensitivity in a target localization task

A localization task required participants to indicate which of 4 locations contained a briefly displayed target. Most displays also contained a distractor that was not equally probable in these locations, affecting performance dramatically. Responses were faster when a display had no distractor and almost as fast when the distractor was in its frequent location. Conversely, responses were slower when targets appeared in frequent-distractor locations, even thou targets were equally likely in each location. Negative-priming effects were reliably smaller when targets followed distractors in the frequent-distractor location compared to the rare-distractor location, challenging the episodic-retrieval account Experiment 2 added a 5th location that rarely displayed distractors and never targets, yet responses slowed most when distractors appeared there. The results confirmed that the attentional system is sensitive to first- and higher-order statistical patterns and can make short- and long-term adjustments in preferences based on prior history of inspecting unsuccessful locations.     

The time course of presaccadic attention shifts

The dynamics of the allocation of attention during the preparation of saccadic eye movements was studied in a dual task paradigm. As the primary task, participants had to perform a saccade to letter-like items arranged on a clock face. The secondary task was a 2AFC discrimination task in which a discrimination target (DT) ('E' or '3') was presented among distractors, either at the saccade goal, or at a spatially separate, precued location. In the first experiment, the position of the DT was kept constant within an experimental block, while the saccade target location varied. In the second experiment, the location of the DT was varied while the saccade target remained the same within a block. The data demonstrate that attentional dynamics differs between the experiments--attention can shift to the saccade goal early or late during the saccade preparation period, depending on the task. Immediately before saccade onset, however, discrimination performance at the location of the saccade target is always superior to other locations, arguing for a strict and selective coupling between saccade preparation and attention.     

Effect of distractor sounds on the auditory attentional blink

Four experiments were conducted to determine whether or not the presence and placement of distractors in a rapid serial auditory stream has any influence on the emergence of the auditory attentional blink (AB). Experiment 1 revealed that the presence of distractors is necessary to produce the auditory AB. In Experiments 2 and 3, the auditory AB was reduced when the distractor immediately following the probe was replaced by silence but not when the distractor following the target was replaced by silence. Finally, in Experiment 4, only a very small auditory AB was found to remain when all distractors following the probe were replaced by silence. These results suggest that the auditory AB is affected both by the overwriting of the probe by the distractors following it and by a reduction in discriminability generated by all of the distractors presented in the sequence.     

Phonological encoding in the attentional blink paradigm

The attentional blink refers to a deficit in reporting a second target that follows a first target within a few hundred milliseconds, when both targets occur in a sequence of distractors shown serially at rates of about 10 items per second. In four experiments, phonological similarity of post-Target 1 distractors impaired dual target report within the interval in which the attentional blink occurs. Similarity of letter targets had a smaller, less reliable effect on performance. Phonological similarity of letter distractors did not affect single target identification (Experiment 3), but it continued to impair dual target report (Experiment 5), even when the targets belonged to a different category—namely, digits. The results demonstrated that, not only targets, but also distractors are encoded phonologically, despite the fact that distractors are irrelevant and never have to be reported.     

视觉工作记忆负载对听觉偏差干扰效应的调控：来自不同外周提示线索的证据

采用线索提示和视听Oddball结合的实验设计, 通过四个实验探讨了外周视线索下视觉工作记忆负载对听觉偏差干扰效应的调控作用。结果表明：(1)操作外周视线索有效性为50%的条件下, 视觉工作记忆负载的增加使得原本抑制无关声音的过程失败, 因此出现了显著的听觉偏差干扰效应; (2)操作外周视线索有效性为80%的条件下, 发现有策略性的注意定向消耗了注意资源, 无视觉工作记忆负载的情况下同样出现听觉偏差干扰, 并且随着工作记忆负载增加偏差干扰效应增强。研究说明视觉工作记忆负载对听觉偏差干扰的调控是有条件性的, 当来自不同感觉通道的无关刺激与目标的加工过程存在重叠时, 视觉工作记忆负载的增加使得听觉偏差干扰效应增强而不是减弱。     

Reaching beyond spatial perception: Effects of intended future actions on visually guided prehension

Three experiments examined whether manipulating actors' intentions, regarding forthcoming actions, influences the time course and kinematics of visually guided, reach‐to‐grasp movements. Subjects performed two‐step action sequences where the initial movement always involved reaching for and grasping cubes located at a constant distance. Demands of the second movement were systematically manipulated. Although the spatial parameters (cube size and distance) remained constant across all conditions, the durations of the initial movements differed substantially depending on the actions subjects intended to perform once the objects were in hand. Less time was required to engage a small (1 cm³) cube when the intention was to transport it to a new location on the workspace vs. a large (4 cm³) cube when the goal was to merely lift it above its current resting position (Experiment 1). This difference in duration of the initial movement reflects more time spent in the deceleration phase of the reach when the task does not require transporting the cube to a new location on the workspace. Further, this context effect is not related to accuracy demands (Experiment 2), or complexity (Experiment 3) of the intended second movement. These findings demonstrate that actions are determined both by the perceived spatial demands of the immediate movement as well as the intended goal of the entire action sequence.     

Incidental and intentional visual memory: What memories are and are not affected by encoding tasks?

Prior research into the impact of encoding tasks on visual memory (Castelhano & Henderson, 2005) indicated that incidental and intentional encoding tasks led to similar memory performance. The current study investigated whether different encoding tasks impacted visual memories equally for all types of objects in a conjunction search (e.g., targets, colour distractors, object category distractors, or distractors unrelated to the target). In sequences of pictures, participants searched for prespecified targets (e.g., green apple; Experiment 1), memorized all objects (Experiment 2), searched for specified targets while memorizing all objects (Experiment 3), searched for postidentified targets (Experiment 4), or memorized all objects with one object prespecified (Experiment 5). Encoding task significantly improved visual memory for targets and led to worse memory for unrelated distractors, but did not influence visual memory of distractors that were related to the target's colour or object category. The differential influence of encoding task indicates that the relative importance of the object both positively and negatively influences the memory retained.