Eye movement suppression interferes with construction of object-centered spatial reference frames in working memory

The brain’s frontal eye fields (FEF), responsible for eye movement control, are known to be involved in spatial working memory (WM).In a previous fMRI experiment (Wallentin, Roepstorff & Burgess, Neuropsychologia, 2008) it was found that FEF activation was primarily related to the formation of an object-centered, rather than egocentric, spatial reference frame. In this behavioral experiment we wanted to demonstrate a causal relationship between eye movement control and manipulation of spatial reference frames. Sixty-two participants recalled either spatial (“Was X in front of Y?”) or non-spatial (“Was X darker than Y?”) relations in a previously shown image containing two to four objects, each with an intrinsic orientation and unique luminance. During half of all recall trials a moving visual stimulus was presented, which participants had to ignore, thus suppressing eye movement. Response times were significantly slower for spatial relations with distraction while there was no effect on non-spatial relations. There was no effect on accuracy, i.e. WM maintenance. This is consistent with the hypothesis that in spatial representations the FEFs are involved in WM content manipulation, such as establishing an object-centered spatial frame of reference.     

Catching a glimpse of working memory: top-down capture as a tool for measuring the content of the mind

This article outlines a methodology for probing working memory (WM) content in high-level cognitive tasks (e.g., decision making, problem solving, and memory retrieval) by capitalizing on attentional and oculomotor biases evidenced in top-down capture paradigms. This method would be of great use, as it could measure the information resident in WM at any point in a task and, hence, track information use over time as tasks dynamically evolve. Above and beyond providing a measure of information occupancy in WM, such a method would benefit from sensitivity to the specific activation levels of individual items in WM. This article additionally forwards a novel fusion of standard free recall and visual search paradigms in an effort to assess the sensitivity of eye movements in top-down capture, on which this new measurement technique relies, to item-specific memory activation (ISMA). The results demonstrate eye movement sensitivity to ISMA in some, but not all, cases.     

颜色和形状工作记忆对非空间返回抑制效应的影响

为进一步考察非空间返回抑制效应是否受工作记忆内容的影响,分别采用颜色和形状工作记忆内容,通过两个实验考察了工作记忆对非空间返回抑制效应的影响。实验结果表明,在颜色和形状工作记忆条件下,均产生了颜色或形状返回抑制效应,并且颜色或形状返回抑制效应量之间均无显著差异,颜色和形状工作记忆内容只增加了判断靶刺激的反应时。研究结论对进一步认识工作记忆内容与非空间返回抑制效应之间的关系有重要参考价值。     

Working memory capacity and the antisaccade task: individual differences in voluntary saccade control

Performance on antisaccade trials requires the inhibition of a prepotent response (i.e., don't look at the flashing cue) and the generation and execution of a correct saccade in the opposite direction. The authors attempted to further specify the role of working memory (WM) span differences in the antisaccade task. They tested high- and low-span individuals on variants of prosaccade and antisaccade trials in which an eye movement is the sole requirement. In 3 experiments, they demonstrated the importance of WM span differences in both suppression of a reflexive saccade and generation of a volitional eye movement. The results support the contention that individual differences in WM span are not exclusively due to differences in inhibition but also reflect differences in directing the focus of attention.     

Attention-referenced visual representations: evidence from impaired visual localization

Spatial representations in the visual system were probed in 4 experiments involving A. H., a woman with a developmental deficit in localizing visual stimuli. Previous research (M. McCloskey et al., 1995) has shown that A. H.'s localization errors take the form of reflections across a central vertical or horizontal axis (e.g., a stimulus 30 degrees to her left localized to a position 30 degrees to her right). The present experiments demonstrate that A. H.'s errors vary systematically as a function of where her attention is focused, independent of how her eyes, head, or body are oriented, or what potential reference points are present in the visual field. These results suggest that the normal visual system constructs attention-referenced spatial representations, in which the focus of attention defines the origin of a spatial coordinate system. A more general implication is that some of the brain's spatial representations take the form of coordinate systems.     

Eye movements disrupt spatial but not visual mental imagery

It has long been known that eye movements are functionally involved in the generation and maintenance of mental images. Indeed, a number of studies demonstrated that voluntary eye movements interfere with mental imagery tasks (e.g., Laeng and Teodorescu in Cogn Sci 26:207–231, 2002). However, mental imagery is conceived as a multifarious cognitive function with at least two components, a spatial component and a visual component. The present study investigated the question of whether eye movements disrupt mental imagery in general or only its spatial component. We present data on healthy young adults, who performed visual and spatial imagery tasks concurrently with a smooth pursuit. In line with previous literature, results revealed that eye movements had a strong disruptive effect on spatial imagery. Moreover, we crucially demonstrated that eye movements had no disruptive effect when participants visualized the depictive aspects of an object. Therefore, we suggest that eye movements serve to a greater extent the spatial than the visual component of mental imagery.     

Working memory load and distraction: dissociable effects of visual maintenance and cognitive control

We establish a new dissociation between the roles of working memory (WM) cognitive control and visual maintenance in selective attention as measured by the efficiency of distractor rejection. The extent to which focused selective attention can prevent distraction has been shown to critically depend on the level and type of load involved in the task. High perceptual load that consumes perceptual capacity leads to reduced distractor processing, whereas high WM load that reduces WM ability to exert priority-based executive cognitive control over the task results in increased distractor processing (e.g., Lavie, Trends in Cognitive Sciences, 9(2), 75–82, 2005). WM also serves to maintain task-relevant visual representations, and such visual maintenance is known to recruit the same sensory cortices as those involved in perception (e.g., Pasternak & Greenlee, Nature Reviews Neuroscience, 6(2), 97–107, 2005). These findings led us to hypothesize that loading WM with visual maintenance would reduce visual capacity involved in perception, thus resulting in reduced distractor processing—similar to perceptual load and opposite to WM cognitive control load. Distractor processing was assessed in a response competition task, presented during the memory interval (or during encoding; Experiment 1a) of a WM task. Loading visual maintenance or encoding by increased set size for a memory sample of shapes, colors, and locations led to reduced distractor response competition effects. In contrast, loading WM cognitive control with verbal rehearsal of a random letter set led to increased distractor effects. These findings confirm load theory predictions and provide a novel functional distinction between the roles of WM maintenance and cognitive control in selective attention.     

Effects of movement duration and visual feedback on visual and proprioceptive components of prism adaptation

While looking through laterally displacing prisms, subjects pointed sagittally 80 times at an objectively straight-ahead target, completing a reciprocal out-and-back pointing movement ever 1, 3, or 6 s. Visual feedback was available early in the pointing movement or only late at the end of the movement. Aftereffect measures of adaptive shift (obtained after every 10 pointing trials) showed adaptive change only in limb position sense (i.e., proprioceptive adaptation) when movement duration was 1 s, regardless of visual feedback condition; but as movement duration increased, adaptive change in the eye position sense (i.e., visual adaptation) increased while proprioceptive adaptation decreased, especially for the late visual feedback condition. Regardless of visual feedback condition, proprioceptive adaptation showed the maximal rate of growth with the 1-s movement duration, whereas visual adaptation showed maximal growth with the 6-s movement duration. These results provide additional support for a model of adaptive spatial mapping in which the direction of strategically flexible coordination (guidance) between eye and limb (and consequently the locus of adaptive spatial mapping) is jointly determined by movement duration and timing of visual feedback. An additional effect of movement duration is to determine the rate of discordant inputs. Maximal growth of adaptation occurs when the input rate matches the response time of the spatial mapping function.     

Effects of Movement Duration and Visual Feedback on Visual and Proprioceptive Components of Prism Adaptation

While looking through laterally displacing prisms, subjects pointed sagittally 80 times at an objectively straight-ahead target, completing a reciprocal out-and-back pointing movement every 1, 3, or 6 s. Visual feedback was available early in the pointing movement or only late at the end of movement. Aftereffect measures of adaptive shift (obtained after every 10 pointing trials) showed adaptive change only in limb position sense (i.e., proprioceptive adaptation) when movement duration was 1 s, regardless of visual feedback condition; but as movement duration increased, adaptive change in the eye position sense (i.e., visual adaptation) increased while proprioceptive adaptation decreased, especially for the late visual feedback condition. Regardless of visual feedback condition, proprioceptive adaptation showed the maximal rate of growth with the 1-s movement duration, whereas visual adaptation showed maximal growth with the 6-s movement duration. These results provide additional support for a model of adaptive spatial mapping in which the direction of strategically flexible coordination (guidance) between eye and limb (and consequently the locus of adaptive spatial mapping) is jointly determined by movement duration and timing of visual feedback. An additional effect of movement duration is to determine the rate of discordant inputs. Maximal growth of adaptation occurs when the input rate matches the response time of the spatial mapping function.     

A Simon effect in memory retrieval: Evidence for the response-discrimination account

According to the traditional view, the effects of irrelevant stimulus location on the selection of a spatial response to a nonspatial stimulus feature (Simon effect) result from long-term associations between spatial stimulus codes and spatially corresponding response codes. According to an alternative view, the response-discrimination account, Simon effects arise from interactions between spatial stimulus codes and response labels in working memory (WM). The latter account predicts Simon effects when participants use spatial labels for response representation in WM, even when the actual responses have no spatial features (e.g., saying the word "plate"). The prediction was tested in an experiment, in which participants first encoded two words at different locations, and then responded to a stimulus by saying the word from the location indicated by stimulus color. The manipulation concerned the correspondence between irrelevant location of the colored stimulus and the retrieval cue for the vocal responses (i.e., word location in the encoding display). A Simon effect in memory retrieval was observed, supporting the response-discrimination account.     

Novel n-back spatial working memory task using eye movement response

We created a novel eye movement version of the n-back task to measure spatial working memory (WM). Rather than one continuous trial, discrete trials were presented in order to develop a simpler WM task. In Experiment 1, we varied the visibility of the final stimulus to maximize the difference in performance between 0-back and 1-back tasks (WM effect). In Experiment 2, we administered the optimized task to children. In Experiment 3, we further simplified the task. Both adults and children easily completed our task, displaying significant WM effects. Further, similar WM effects were obtained in our original and simplified n-back spatial WM tasks, demonstrating flexibility. Because WM deficits are often an early feature of disease and a marker of disease progression, our saccadic measure of spatial WM may be particularly useful in hard-to-test populations, such as patients and children, and may have application in brain-imaging studies that require discrete trials.     

On the timing basis of bimanual coordination in discrete and continuous tasks.

Motor events are behaviorally meaningful, discrete entities (e.g., key strokes) that are generated at some specific portion of an effector's movement trajectory. Bimanual coordination may be conceptualized with reference to such discrete motor events or with reference to continuous movement trajectories. Studies inspired by the former approach suggest that hand coordination is primarily achieved by assigning a coherent timing goal structure to the motor events produced by each hand. Studies conducted with the latter approach have shown that between-hand interdependence may also arise from the cross-coupling of the command signals that generate each hand's motion. Little is known, however, about the relationships between timing-level coordination and trajectory-level coordination of the hands. Some aspects of these relationships are analyzed using data from experiments that involved bimanual finger tapping and circle drawing at identical and different frequencies.     

Exploiting human sensitivity to gaze for tracking the eyes

Given the prevalence, quality, and low cost of web cameras, along with the remarkable human sensitivity to gaze, we examined the accuracy of eye tracking using only a web camera. Participants were shown webcamera recordings of a person’s eyes moving 1°, 2°, or 3° of visual angle in one of eight radial directions (north, northeast, east, southeast, etc.), or no eye movement occurred at all. Observers judged whether an eye movement was made and, if so, its direction. Our findings demonstrate that for all saccades of any size or direction, observers can detect and discriminate eye movements significantly better than chance. Critically, the larger the saccade, the better the judgments, so that for eye movements of 3°, people can tell whether an eye movement occurred, and where it was going, at about 90% or better. This simple methodology of using a web camera and looking for eye movements offers researchers a simple, reliable, and cost-effective research tool that can be applied effectively both in studies where it is important that participants maintain central fixation (e.g., covert attention investigations) and in those where they are free or required to move their eyes (e.g., visual search).     

Reconsidering ‘spatial memory’ and the Morris water maze

The Morris water maze has been put forward in the philosophy of neuroscience as an example of an experimental arrangement that may be used to delineate the cognitive faculty of spatial memory (e.g., Craver and Darden, Theory and method in the neurosciences, University of Pittsburgh Press, Pittsburgh, 2001; Craver, Explaining the brain: Mechanisms and the mosaic unity of neuroscience, Oxford University Press, Oxford, 2007). However, in the experimental and review literature on the water maze throughout the history of its use, we encounter numerous responses to the question of “what” phenomenon it circumscribes ranging from cognitive functions (e.g., “spatial learning”, “spatial navigation”), to representational changes (e.g., “cognitive map formation”) to terms that appear to refer exclusively to observable changes in behavior (e.g., “water maze performance”). To date philosophical analyses of the water maze have not been directed at sorting out what phenomenon the device delineates nor the sources of the different answers to the question of what. I undertake both of these tasks in this paper. I begin with an analysis of Morris’s first published research study using the water maze and demonstrate that he emerged from it with an experimental learning paradigm that at best circumscribed a discrete set of observable changes in behavior. However, it delineated neither a discrete set of representational changes nor a discrete cognitive function. I cite this in combination with a reductionist-oriented research agenda in cellular and molecular neurobiology dating back to the 1980s as two sources of the lack of consistency across the history of the experimental and review literature as to what is under study in the water maze.     

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.     

Representations of interobject spatial relations in long-term memory

A growing body of evidence has indicated that human spatial memory is organized in terms of a small number of reference directions and that interobject spatial relations are represented in terms of these directions (e.g., McNamara, 2003). The goal of the present experiments was to investigate whether the selection of reference directions also affects the fidelity with which interobject spatial relations are represented in memory. In two experiments, participants memorized a layout of nine objects and then performed judgments of relative direction (e.g., “Imagine you are standing at the clock, facing the book. Point to the phone.”) at a remote location. Imagined heading (e.g., at the clock, facing the book) and allocentric target direction (e.g., the direction from clock to phone in the allocentric frame of reference used to define imagined heading) were manipulated independently. The results of both experiments showed that the same directions that were benefited in imagined headings were also benefited in allocentric target directions. These findings indicate that interobject spatial relations are preferentially represented when they coincide with a reference direction.     

Visual rivalry without spatial conflict

Visual rivalry has been extensively characterized in the literature. It is thought to require spatial conflict between overlapping visual presentations, even in studies that have found nonspatial (i.e., nonretinal) influences on rivalry. Unexpectedly, we identified visual rivalry in the complete absence of spatial conflict. Participants experienced visual rivalry when we placed a nonambiguous motion stimulus in a nonspatial (in our case, object-based) reference frame. Moreover, a stimulus that was displaced within a nonspatial reference frame did not induce rivalry despite the presence of spatial conflict. This finding shows that nonspatial, object-based processing can overrule retinotopic processing and prevent rivalry from occurring when a perceived stimulus exists unambiguously in an object-based reference frame. Our results identify a potent high-level conflict-resolution stage independent of low-level spatial visual conflict. This independence of spatial overlap provides an advantage to the visual system, allowing conflict resolution when an object is nonstationary on the retina (e.g., during frequently occurring eye movements).     

习得性空间联结的迁移依赖于语义工作记忆

采用练习迁移范式与双任务范式相结合的设计来探讨练习所习得的空间联结在工作记忆中如何表征。被试先进行不一致空间的刺激—反应映射练习任务, 五分钟后, 随机迁移到单任务(Simon任务)或者双任务(Simon任务+语义工作记忆负荷任务或空间工作记忆负荷任务)。结果发现：不一致的练习能使单任务出现反转的Simon效应, 但语义工作记忆负荷会使反转的Simon效应消失, 而空间工作记忆负荷却对反转的Simon效应没有影响。实验结果表明练习产生的空间联结依赖于语义工作记忆。     

Number sense or working memory? The effect of two computer-based trainings on mathematical skills in elementary school

Research on the improvement of elementary school mathematics has shown that computer-based training of number sense (e.g., processing magnitudes or locating numbers on the number line) can lead to substantial achievement gains in arithmetic skills. Recent studies, however, have highlighted that training domain-general cognitive abilities (e.g., working memory [WM]) may also improve mathematical achievement. This study addressed the question of whether a training of domain-specific number sense skills or domain-general WM abilities is more appropriate for improving mathematical abilities in elementary school. Fifty-nine children (M_age = 9 years, 32 girls and 27 boys) received either a computer-based, adaptive training of number sense (n = 20), WM skills (n = 19), or served as a control group (n = 20). The training duration was 20 min per day for 15 days. Before and after training, we measured mathematical ability using a curriculum-based math test, as well as spatial WM. For both training groups, we observed substantial increases in the math posttest compared to the control group (d = .54 for number sense skills training, d = .57 for WM training, respectively). Whereas the number sense group showed significant gains in arithmetical skills, the WM training group exhibited marginally significant gains in word problem solving. However, no training group showed significant posttest gains on the spatial WM task. Results indicate that a short training of either domain-specific or domain-general skills may result in reliable short-term training gains in math performance, although no stable training effects were found in the spatial WM task.