Impact of action planning on spatial perception: Attention matters

Previous research suggested that perception of spatial location is biased towards spatial goals of planned hand movements. In the present study I show that an analogous perceptual distortion can be observed if attention is paid to a spatial location in the absence of planning a hand movement. Participants judged the position of a target during preparation of a mouse movement, the end point of which could deviate from the target by a varying degree in Exp. 1. Judgments of target position were systematically affected by movement characteristics consistent with perceptual assimilation between the target and the planned movement goal. This effect was neither due to an impact of motor execution on judgments (Exp. 2) nor due to characteristics of the movement cues or of certain target positions (Exp. 3, Exp. 5A). When the task included deployment of attention to spatial positions (former movement goals) in preparation for a secondary perceptual task, an effect emerged that was comparable with the bias associated with movement planning (Exp. 4, Exp. 5B). These results indicate that visual distortions accompanying manipulations of variables related to action could be mediated by attentional mechanisms.     

Planning paths to multiple targets: memory involvement and planning heuristics in spatial problem solving

For large numbers of targets, path planning is a complex and computationally expensive task. Humans, however, usually solve such tasks quickly and efficiently. We present experiments studying human path planning performance and the cognitive processes and heuristics involved. Twenty-five places were arranged on a regular grid in a large room. Participants were repeatedly asked to solve traveling salesman problems (TSP), i.e., to find the shortest closed loop connecting a start location with multiple target locations. In Experiment 1, we tested whether humans employed the nearest neighbor (NN) strategy when solving the TSP. Results showed that subjects outperform the NN-strategy, suggesting that it is not sufficient to explain human route planning behavior. As a second possible strategy we tested a hierarchical planning heuristic in Experiment 2, demonstrating that participants first plan a coarse route on the region level that is refined during navigation. To test for the relevance of spatial working memory (SWM) and spatial long-term memory (LTM) for planning performance and the planning heuristics applied, we varied the memory demands between conditions in Experiment 2. In one condition the target locations were directly marked, such that no memory was required; a second condition required participants to memorize the target locations during path planning (SWM); in a third condition, additionally, the locations of targets had to retrieved from LTM (SWM and LTM). Results showed that navigation performance decreased with increasing memory demands while the dependence on the hierarchical planning heuristic increased.     

Trading off switch costs and stimulus availability benefits: An investigation of voluntary task-switching behavior in a predictable dynamic multitasking environment

In the present study, we introduce a novel, self-organized task-switching paradigm that can be used to study more directly the determinants of switching. Instead of instructing participants to randomly switch between tasks, as in the classic voluntary task-switching paradigm (Arrington & Logan, 2004), we instructed participants to optimize their task performance in a voluntary task-switching environment in which the stimulus associated with the previously selected task appeared in each trial after a delay. Importantly, the stimulus onset asynchrony (SOA) increased further with each additional repetition of this task, whereas the stimulus needed for a task switch was always immediately available. We conducted two experiments with different SOA increments (i.e., Exp. 1a = 50 ms, Exp. 1b = 33 ms) to see whether this procedure would induce switching behavior, and we explored how people trade off switch costs against the increasing availability of the stimulus needed for a task repetition. We observed that participants adapted their behavior to the different task environments (i.e., SOA increments) and that participants switched tasks when the SOA in task switches approximately matched the switch costs. Moreover, correlational analyses indicated relations between individual switch costs and individual switch rates across participants. Together, these results demonstrate that participants were sensitive to the increased availability of switch stimuli in deciding whether to switch or to repeat, which in turn demonstrates flexible adaptive task selection behavior. We suggest that performance limitations in task switching interact with the task environment to influence switching behavior.     

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).     

内外源性空间注意对多感觉整合的影响

本文采用内-外源性空间线索靶子范式, 操控内源性线索有效性(有效线索、无效线索)、外源性线索有效性(有效线索、无效线索)、目标刺激类型(视觉刺激、听觉刺激、视听觉刺激)三个自变量。通过两个不同任务难度的实验(实验1: 简单定位任务; 实验2: 复杂辨别任务)来考察内外源性空间注意对多感觉整合的影响。两个实验结果均发现外源性空间注意显著减弱了多感觉整合效应, 内源性空间注意没有显著增强多感觉整合效应; 实验2中还发现了内源性空间注意会对外源性空间注意减弱多感觉整合效应产生影响。结果表明, 与内源性空间注意不同, 外源性空间注意对多感觉整合的影响不易受任务难度的调控; 当任务较难时内源性空间注意会影响外源性空间注意减弱多感觉整合效应的过程。由此推测, 内外源性空间注意对多感觉整合的调节并非彼此独立、而是相互影响的。     

Performance of unimanual and bimanual multiphased prehensile movements

By manipulating task action demands in 2 experiments, the author investigated whether the context-dependent effects seen in unimanual multiphase movements are also present in bimanual movements. Participants (N = 14) in Experiment 1 either placed or tossed objects into targets. The results indicated that the intention to perform a subsequent action with an object could influence the performance of an earlier movement in a sequence in both unimanual and bimanual tasks. Furthermore, assimilation effects were found when the subsequent tasks being performed by the 2 hands were incongruent. In Experiment 2, the author investigated in 12 participants whether planning in a multiphase movement includes some representation of the accuracy demands of the subsequent task. The accuracy demands of a subsequent task did not appear to influence initial movement planning. Instead, the present results support the notion that it is the action requirements of the subsequent movement that lead to context-dependent effects.     

Practice and assimilation effects in a multilimb aiming task

When two limbs are required to move different distances simultaneously, assimilation effects are shown: The shorter distance limb tends to overshoot the target, whereas the longer distance limb undershoots. The effect of practice on assimilation effects was studied in two experiments, using a simultaneous four-limb aiming task. When subjects were required to move their left limbs a shorter distance than the right (5 cm vs. 9 cm), the right limbs moved a lesser distance and had greater variable and overall errors relative to a group required to move all limbs the same distance (9 cm). Practice reduced assimilation effects in the lower limbs, but spatial assimilations were present throughout 125 acquisition trials with KR and 50 no-KR transfer trials, spanning 24 hours. When the upper limbs were required to move a greater distance than the lower limbs (15 cm vs. 9 cm), the lower limbs showed longer distances and increased overall errors early in practice compared to the lower limbs of a group required to move all limbs 9 cm. With practice, the between-group differences decreased, with no assimilation effects shown on the transfer trials. The results suggest that neural crosstalk is greater between left and right sides than between upper and lower limbs. Results are discussed in light of the functional cerebral space model of simultaneous actions.     

Practice and Assimilation Effects in a Multilimb Aiming Task

When two limbs are required to move different distances simultaneously, assimilation effects are shown: The shorter distance limb tends to overshoot the target, whereas the longer distance limb undershoots. The effect of practice on assimilation effects was studied in two experiments, using a simultaneous four-limb aiming task. When subjects were required to move their left limbs a shorter distance than the right (5 cm vs. 9 cm), the right limbs moved a lesser distance and had greater variable and overall errors relative to a group required to move all limbs the same distance (9 cm). Practice reduced assimilation effects in the lower limbs, but spatial assimilations were present throughout 125 acquisition trials with KR and 50 no-KR transfer trials, spanning 24 hours. When the upper limbs were required to move a greater distance than the lower limbs (15 cm vs. 9 cm), the lower limbs showed longer distances and increased overall errors early in practice compared to the lower limbs of a group required to move all limbs 9 cm. With practice, the between-group differences decreased, with no assimilation effects shown on the transfer trials. The results suggest that neural crosstalk is greater between left and right sides than between upper and lower limbs. Results are discussed in light of the functional cerebral space model of simultaneous actions.     

The role of cognitive control mechanisms in selective attention towards emotional stimuli

The role of cognitive control mechanisms in reducing interference from emotionally salient distractors was investigated. In two experiments, participants performed a flanker task in which target-distractor affective compatibility and cognitive load were manipulated. Differently from past studies, targets and distractors were presented at separate spatial locations and cognitive load was not domain-specific. In Experiment 1, words (positive vs. negative) and faces (angry, happy or neutral faces), were used respectively as targets and distractors, whereas in Experiment 2, both targets (happy vs. angry) and distractors were faces. Findings showed interference from distractor processing only when cognitive load was high. The present findings indicate that, when targets and distractors are presented at different spatial locations, cognitive control mechanisms are involved in preventing interference from positive (Exp. 1) or negative distractors (Exp. 2). The role of stimulus valence and type is also discussed with regard to different patterns of interference observed.     

双通道分配性注意对视听觉返回抑制的影响

本研究基于线索-靶子范式, 操纵目标刺激类型(视觉、听觉、视听觉)与线索有效性(有效线索、中性条件、无效线索)两个自变量, 通过3个实验来考察双通道分配性注意对视听觉返回抑制(inhibition of return, IOR)的影响。实验1 (听觉刺激呈现在左/右侧)结果发现, 在双通道分配性注意条件下, 视觉目标产生显著IOR效应, 而视听觉目标没有产生IOR效应; 实验2 (听觉刺激呈现在左/右侧)与实验3 (听觉刺激呈现在中央)结果发现, 在视觉通道选择性注意条件下, 视觉与视听觉目标均产生显著IOR效应但二者无显著差异。结果表明：双通道分配性注意减弱视听觉IOR效应。     

Conflict's consequences: effects of social motives on postnegotiation creative and convergent group functioning and performance

Two studies tested the effects of social motives during negotiation on postnegotiation group performance. In both experiments, a prosocial or a proself motivation was induced, and participants negotiated in 3-person groups about a joint market. In Experiment 1, groups subsequently performed an advertisement task. Consistent with the authors' predictions, results showed that proself groups performed worse on the convergent aspects of this task but better on the divergent aspects than prosocial groups. In Experiment 2, the authors manipulated social motive and negotiation (negotiation vs. no negotiation), and groups performed a creativity task (requiring divergent performance) or a planning task (requiring convergent performance). Proself groups showed greater dedication, functioned more effectively, and performed better than prosocial groups on the creativity task, whereas prosocial groups showed greater dedication, functioned more effectively, and performed better than proself groups on the planning task, and these effects only occurred when the task was preceded by group negotiation.     

The effects of sequence difficulty and practice on proportional and nonproportional transfer

Two experiments were designed to determine participants' ability to transfer a learned movement sequence to new spatial locations. A 16-element dynamic arm movement sequence was used in both experiments. The task required participants to move a horizontal lever to sequentially projected targets. Experiment 1 included two groups. One group practised a relatively easy 16-element movement sequence (easy long). The other group practised a more difficult 16-element movement sequence (difficult long). Approximately 24 hours after practice with their respective sequence both groups were administered a retention and two transfer tests. The only difference between the retention and transfer tests was the location of the targets. The short transfer target configuration was considered a proportional transfer because all the amplitudes between targets were reduced by the same proportion. The mixed transfer configuration was considered a nonproportional transfer because the targets did not have the same proportional distances between targets as the sequence they practised. The results indicated that participants could effectively transfer the difficult long sequence to the new target configurations regardless of whether the transfer required proportional and nonproportional spatial changes to the movement pattern. However, the easy long sequence was only effectively transferred in the proportional transfer condition. Experiment 2 assessed the effects of extended practice of the easy long sequence on proportional and nonproportional spatial transfer. The data indicated that participants could again effectively transfer the easy long sequence to proportional but not the nonproportional spatial transfer conditions regardless of the amount of practice (1 or 4 days). The results are discussed in terms of the mechanism by which response sequences become increasingly specific over extended practice in an attempt to optimize movement production and how this process interacts with the difficulty of the sequence.     

Proportional and nonproportional transfer of movement sequences

Two experiments were designed to determine participants' ability to transfer a learned movement sequence to new spatial locations. A 16-element dynamic arm movement sequence was used in both experiments. The task required participants to move a horizontal lever to sequentially projected targets. Experiment 1 included 2 groups. One group practised a pattern in which targets were located at 20, 40, 60, and 80° from the start position (long sequence). The other group practised a pattern with targets at 20, 26.67, 60, and 80° (mixed sequence). Both groups were tested 24 hours later on the long, mixed, and short sequence. The short sequence was considered a proportional transfer for the long acquisition group because all the amplitudes between targets were reduced by the same proportion. Nonproportional transfer occurred when the amplitudes between targets did not have the same proportions as those for their practice sequence (e.g., long sequence to mixed sequence or vice versa). The results indicated that participants could effectively transfer to new target configurations regardless of whether the transfer required proportional or nonproportional spatial changes to the movement pattern. Experiment 2 assessed the effects of extended practice on proportional and nonproportional spatial transfer. The data indicated that while participants can effectively transfer to both proportional and nonproportional spatial transfer conditions after 1 day of practice, they are only effective at transferring to proportional transfer conditions after 4 days of practice. The results are discussed in terms of the mechanism by which response sequences become increasingly specific over extended practice in an attempt to optimize movement production.     

Keys and seats: Spatial response coding underlying the joint spatial compatibility effect

Spatial compatibility effects (SCEs) are typically observed when participants have to execute spatially defined responses to nonspatial stimulus features (e.g., the color red or green) that randomly appear to the left and the right. Whereas a spatial correspondence of stimulus and response features facilitates response execution, a noncorrespondence impairs task performance. Interestingly, the SCE is drastically reduced when a single participant responds to one stimulus feature (e.g., green) by operating only one response key (individual go/no-go task), whereas a full-blown SCE is observed when the task is distributed between two participants (joint go/no-go task). This joint SCE (a.k.a. the social Simon effect) has previously been explained by action/task co-representation, whereas alternative accounts ascribe joint SCEs to spatial components inherent in joint go/no-go tasks that allow participants to code their responses spatially. Although increasing evidence supports the idea that spatial rather than social aspects are responsible for joint SCEs emerging, it is still unclear to which component(s) the spatial coding refers to: the spatial orientation of response keys, the spatial orientation of responding agents, or both. By varying the spatial orientation of the responding agents (Exp. 1) and of the response keys (Exp. 2), independent of the spatial orientation of the stimuli, in the present study we found joint SCEs only when both the seating and the response key alignment matched the stimulus alignment. These results provide evidence that spatial response coding refers not only to the response key arrangement, but also to the—often neglected—spatial orientation of the responding agents.     

Proportional and nonproportional transfer of movement sequences

Two experiments were designed to determine participants' ability to transfer a learned movement sequence to new spatial locations. A 16-element dynamic arm movement sequence was used in both experiments. The task required participants to move a horizontal lever to sequentially projected targets. Experiment 1 included 2 groups. One group practised a pattern in which targets were located at 20, 40, 60, and 80° from the start position (long sequence). The other group practised a pattern with targets at 20, 26.67, 60, and 80° (mixed sequence). Both groups were tested 24 hours later on the long, mixed, and short sequence. The short sequence was considered a proportional transfer for the long acquisition group because all the amplitudes between targets were reduced by the same proportion. Nonproportional transfer occurred when the amplitudes between targets did not have the same proportions as those for their practice sequence (e.g., long sequence to mixed sequence or vice versa). The results indicated that participants could effectively transfer to new target configurations regardless of whether the transfer required proportional or nonproportional spatial changes to the movement pattern. Experiment 2 assessed the effects of extended practice on proportional and nonproportional spatial transfer. The data indicated that while participants can effectively transfer to both proportional and nonproportional spatial transfer conditions after 1 day of practice, they are only effective at transferring to proportional transfer conditions after 4 days of practice. The results are discussed in terms of the mechanism by which response sequences become increasingly specific over extended practice in an attempt to optimize movement production.     

Nomadic inhibition of attention and motor responses

Klein and MacInnes [Klein, R. M., & MacInnes, W. J. (1999). Inhibition of return is a foraging facilitator in visual search. Psychological Science, 10, 346-352] posited that the function of a phenomenon known as the inhibition of return (IOR) [Posner, M. I., & Cohen, Y. (1984). Components of visual orienting. In H. Bouma, & D. G. Bouwhuis (Eds.), Attention and performance X: Control of language processes (pp. 531-554). Hillsdale, NJ: Erlbaum] is to facilitate the foraging of food and objects in the environment. Once a target object has been identified either the location of that target in space or a movement to that target is inhibited in order to allow the performer to shift his/her attention to something new. Interestingly, in the majority of IOR studies, participants begin their search from a central home position. This research examined IOR in a nomadic target-target paradigm in which the home position randomly appeared at one of three target locations and attentional shifts/movements progressed to other locations. In Experiment 1, participants executed simple manual button presses in response to the sequential presentation of a home position and then two target stimuli. In Experiment 2, participants made manual-aiming movements in response to the same type of presentation. Results obtained from both experiments implicate perceptual-motor mechanisms over and above the inhibition of a specific target location or response. Inhibitory effects appear to be associated with both perceptual and motor processes, and depend not only on the temporal and spatial relations between potential targets, but also on the actions required to detect or engage the targets.     

Working memory representations persist in the face of unexpected task alterations

It is well known that information can be held in memory while performing other tasks concurrently, such as remembering a color or number during a separate visual search task. However, it is not clear what happens to stored information in the face of unexpected tasks, such as the surprise questions that are often used in experiments related to inattentional and change blindness. Does the unpredicted shift in task context cause memory representations to be cleared in anticipation of new information? To answer this question, we ran two experiments where the task unexpectedly switched partway through the experiment with a surprise question. Half of the participants were asked to report the same attribute (Exp. 1?=?Identity, Exp. 2?=?Color) of a target stimulus in both presurprise and postsurprise trials, while for the other half, the reported attribute switched from identity to color (Exp. 1) or vice versa (Exp. 2). Importantly, all participants had to read an unexpected set of instructions and respond differently on the surprise trial. Accuracy on the surprise trial was higher for the same-attribute groups than the different-attribute groups. Furthermore, there was no difference in reaction time on the surprise trial between the two groups. These results suggest that information participants expected to report can survive an encounter with an unexpected task. The implication is that failures to report information on a surprise trial in many experiments reflect genuine differences in memory encoding, rather than forgetting or overwriting induced by the surprise question.     

The effects of sequence difficulty and practice on proportional and nonproportional transfer

Two experiments were designed to determine participants' ability to transfer a learned movement sequence to new spatial locations. A 16-element dynamic arm movement sequence was used in both experiments. The task required participants to move a horizontal lever to sequentially projected targets. Experiment 1 included two groups. One group practised a relatively easy 16-element movement sequence (easy long). The other group practised a more difficult 16-element movement sequence (difficult long). Approximately 24 hours after practice with their respective sequence both groups were administered a retention and two transfer tests. The only difference between the retention and transfer tests was the location of the targets. The short transfer target configuration was considered a proportional transfer because all the amplitudes between targets were reduced by the same proportion. The mixed transfer configuration was considered a nonproportional transfer because the targets did not have the same proportional distances between targets as the sequence they practised. The results indicated that participants could effectively transfer the difficult long sequence to the new target configurations regardless of whether the transfer required proportional and nonproportional spatial changes to the movement pattern. However, the easy long sequence was only effectively transferred in the proportional transfer condition. Experiment 2 assessed the effects of extended practice of the easy long sequence on proportional and nonproportional spatial transfer. The data indicated that participants could again effectively transfer the easy long sequence to proportional but not the nonproportional spatial transfer conditions regardless of the amount of practice (1 or 4 days). The results are discussed in terms of the mechanism by which response sequences become increasingly specific over extended practice in an attempt to optimize movement production and how this process interacts with the difficulty of the sequence.     

Spatial reasoning with external visualizations: what matters is what you see, not whether you interact

Three experiments examined the effects of interactive visualizations and spatial abilities on a task requiring participants to infer and draw cross sections of a three-dimensional (3D) object. The experiments manipulated whether participants could interactively control a virtual 3D visualization of the object while performing the task, and compared participants who were allowed interactive control of the visualization to those who were not allowed control. In Experiment 1, interactivity produced better performance than passive viewing, but the advantage of interactivity disappeared in Experiment 2 when visual input for the two conditions in a yoked design was equalized. In Experiments 2 and 3, differences in how interactive participants manipulated the visualization were large and related to performance. In Experiment 3, non-interactive participants who watched optimal movements of the display performed as well as interactive participants who manipulated the visualization effectively and better than interactive participants who manipulated the visualization ineffectively. Spatial ability made an independent contribution to performance on the spatial reasoning task, but did not predict patterns of interactive behavior. These experiments indicate that providing participants with active control of a computer visualization does not necessarily enhance task performance, whereas seeing the most task-relevant information does, and this is true regardless of whether the task-relevant information is obtained actively or passively.