视觉工作记忆负载类型对注意选择的影响

通过操纵Flanker任务相对于视觉工作记忆任务的呈现位置, 探讨在视觉工作记忆编码和保持阶段, 精度负载和容量负载对注意选择的影响。行为结果发现, Flanker任务呈现位置和视觉工作记忆负载类型影响注意选择; ERP结果发现, 在保持阶段, 当搜索目标和干扰项不一致时, 负载类型影响N2成分。研究表明, 在编码阶段, 视觉工作记忆负载主要通过占用更多知觉资源降低干扰效应, 支持知觉负载理论; 而在保持阶段, 当Flanker任务位于记忆项内部时, 两类负载在工作记忆表征过程中不同的神经活动导致投入到注意选择的认知控制资源不同, 可能是两类负载影响保持阶段注意选择的机制。     

听觉丧失对听障学生时间知觉的影响

本研究采用同时判断任务和时距二分任务,探讨了听觉丧失对听障学生视觉通道的时间知觉的影响及其机制。两个系列实验结果表明,听觉丧失损伤了听障学生视觉通道的时序知觉准确性、敏感性以及时距知觉的敏感性,支持了普遍缺陷假设;但是,听障学生视觉通道的时距知觉的准确性却未受到听觉丧失的显著影响,支持了知觉补偿假设。因此,听觉丧失对听障学生视觉通道的时间知觉的影响可能是基于选择性的机制,这主要取决于不同的时间任务以及知觉属性等因素。     

视觉时距知觉序列依赖效应的空间迁移性

个体当前的知觉反应不仅取决于当前的刺激输入,而且依赖于先前的感知经验,可表现为知觉的序列依赖效应。结合时距二分任务,通过3个实验系统改变先前试次和当前试次中刺激的位置关系,考察了时距知觉的序列依赖效应及其空间迁移性。结果发现,(1)先前试次的刺激时距导致了排斥性的刺激序列依赖效应,并且这种效应能够完全迁移到不同的空间位置;(2)先前试次的决策反应导致了吸引性的决策序列依赖效应,但该效应仅能部分迁移到不同的空间位置;(3)时距知觉的刺激和决策序列依赖效应的空间迁移性不受空间类型(外部空间vs.视网膜空间)的调节。这些结果在一定程度上反映了视觉时距知觉序列依赖效应产生的潜在神经位置:刺激序列依赖效应可能产生于对空间信息不敏感或具有较大感受野的较高级视觉加工脑区;决策序列依赖效应则可能源于具有类别组织功能的高级认知脑区。     

位置特异性和项目呈现方式对即时情景记忆顺序重构的影响

在Healy等人(2008)的实验范式基础上,以中文姓名作为实验材料,探究位置特异性和项目呈现方式对即时情景记忆的影响。两个实验都要求被试对所呈现的20个姓名中的12个进行顺序重构。重构的12个位置分别为1-12、5-16、9-20三个水平,这三组位置同时包括绝对位置9-12。实验1采取视觉呈现,比较三个任务类型上重构正确率的差异。实验1的结果支持Healy的编码特异性理论,但是末尾呈现的项目仅有较小的重构优势。实验2采取听觉呈现,结果发现,在系列位置5-16上出现了较明显的近因效应,而在位置9-20上并无明显的近因效应。这表明位置特异性理论对顺序重构的影响主要表现为绝对位置的特异性而并非相对位置的特异性,系列位置效应出现在记忆的编码过程而不是提取过程。     

时距知觉的扭曲:新异刺激效应

时距知觉会受到刺激新异性的影响,新异刺激的呈现时间往往被认为长于等时距重复出现的标准刺激的呈现时间.已有研究在解释这种主观的时距扩张现象时主要涉及三种假设:注意假设、唤醒假设和神经编码效能假设.研究中的变量混淆问题、跨通道效应和时间因素是今后研究中值得思考的几个问题.对于新异刺激效应产生的心理和神经机制,研究者们还存在着较大分歧.进一步探讨其心理和神经机制对理解时距知觉具有重要意义.     

知觉负载对注视知觉适应后效的影响

结合知觉负载任务和注视适应范式,考察了知觉负载(高、低知觉负载)对不同注视线索(偏离注视与直视)适应后效的影响。结果发现:(1)偏离注视在低负载条件存在显著的适应后效,而在高负载条件仅存在微弱的适应后效,并且前者显著大于后者;(2)直视在低负载和高负载条件都出现了显著的适应后效,并且二者不存在显著差异;(3)注意资源对偏离注视知觉的调节作用大于对直视知觉的作用。这说明,偏离注视知觉受到注意资源紧张程度的调节,而直视知觉不受注意资源的调节,注意资源对直视与偏离注视的调节作用存在差异,推测二者可能存在不同的加工机制。     

单眼和双眼特定的McCollough效应及倾斜后效的消退过程

每个被试对互补的联合方位的图形适应后均产生单眼特定和双眼特定的McCollough效应。双眼的起始强度大于单眼的起始强度。单眼和双眼的McCollough效应的消退速度基本相同。在自然视觉条件下McCollough效应消退快,在完全黑暗的条件下没有明显的消退。说明导致McCollough效应恢复平衡的主要因素不是自发的过程,而与网膜刺激有关。倾斜知觉后效的消退在上述两种实验条件下没有明显的差别,因此可推测倾斜知觉后效的消退主要是神经疲劳的一个自发的恢复过程。     

数量适应后效的皮层映射特征

本研究探讨了观察者与观察目标存在相对运动时视觉系统对目标数量特征的适应后效的皮层映射特征, 并与对比度适应后效的映射规律进行比较。包括两项实验。其中, 实验一要求被试在适应目标后转换注视点, 考察眼跳后相同和不同视网膜区域以及相同和不同空间区域的适应后效, 发现数量适应后效具有部分空间-皮层映射特性, 而对比度适应后效则表现出完全的视网膜-皮层映射特征。实验二采用固定的注视点, 考察目标运动后目标原位置和新位置区域的适应后效, 发现数量适应后效不完全依赖于视网膜-皮层映射, 它可以“追随”客体运动重新映射到新的位置, 表现出基于客体映射的特征, 而对比度适应后效则完全依赖于视网膜-皮层映射, 不能“追随”客体移动在目标新位置重新形成映射。两项实验结果提示, 相对于对比度等低级表面特征而言, 数量特征对目标的描述涉及更高的加工水平, 它可以与观察目标的相对运动信息进行整合, 且这种整合在眼跳和非眼跳的观察条件下都可发生。     

适应范式在人脸知觉研究中的应用

适应范式为考察各种心理现象或心理过程的机制提供了一条重要的途径。本文在简要介绍传统适应范式和功能性磁共振适应范式的基础上,重点回顾了它们在人脸知觉研究中的应用,提出人脸适应后效除源于尺寸和朝向等低、中水平物理信息的编码加工外,更多地基于身份和性别等高水平社会信息的编码,且其效应量依赖于高水平的基于标准的竞争性编码加工机制。对人脸类别属性的编码标准和时效性等问题仍有待进一步分析。     

知觉启动效应及其脑机制的研究进展

该文从三个方面对知觉启动效应研究进行了回顾：(1)知觉启动的一般特征：(2)刺激的物理特征与知觉启动之间的关系;(3)知觉启动的神经解剖基础及神经机制。该文指出．知觉启动主要加工刺激表面的物理特征;刺激的大小、位置、颜色、模式等特征尽管对知觉启动有影响．但刺激的形状和结构等特征对于知觉启动更重要;知觉启动主要受枕部皮层的调节。最后,讨论了几个有关知觉启动机制的理论假说。     

Audition dominates vision in duration perception irrespective of salience,attention, and temporal discriminability

Whereas the visual modality tends to dominate over the auditory modality in bimodal spatial perception, the auditory modality tends to dominate over the visual modality in bimodal temporal perception. Recent results suggest that the visual modality dominates bimodal spatial perception because spatial discriminability is typically greater for the visual than for the auditory modality; accordingly, visual dominance is eliminated or reversed when visual-spatial discriminability is reduced by degrading visual stimuli to be equivalent or inferior to auditory spatial discriminability. Thus, for spatial perception, the modality that provides greater discriminability dominates. Here, we ask whether auditory dominance in duration perception is similarly explained by factors that influence the relative quality of auditory and visual signals. In contrast to the spatial results, the auditory modality dominated over the visual modality in bimodal duration perception even when the auditory signal was clearly weaker, when the auditory signal was ignored (i.e., the visual signal was selectively attended), and when the temporal discriminability was equivalent for the auditory and visual signals. Thus, unlike spatial perception, where the modality carrying more discriminable signals dominates, duration perception seems to be mandatorily linked to auditory processing under most circumstances.     

To what extent do Gestalt grouping principles influence tactile perception?

Since their formulation by the Gestalt movement more than a century ago, the principles of perceptual grouping have primarily been investigated in the visual modality and, to a lesser extent, in the auditory modality. The present review addresses the question of whether the same grouping principles also affect the perception of tactile stimuli. Although, to date, only a few studies have explicitly investigated the existence of Gestalt grouping principles in the tactile modality, we argue that many more studies have indirectly provided evidence relevant to this topic. Reviewing this body of research, we argue that similar principles to those reported previously in visual and auditory studies also govern the perceptual grouping of tactile stimuli. In particular, we highlight evidence showing that the principles of proximity, similarity, common fate, good continuation, and closure affect tactile perception in both unimodal and crossmodal settings. We also highlight that the grouping of tactile stimuli is often affected by visual and auditory information that happen to be presented simultaneously. Finally, we discuss the theoretical and applied benefits that might pertain to the further study of Gestalt principles operating in both unisensory and multisensory tactile perception.     

Rapid adaptation to auditory-visual spatial disparity

The so-called ventriloquism aftereffect is a remarkable example of rapid adaptative changes in spatial localization caused by visual stimuli. After exposure to a consistent spatial disparity of auditory and visual stimuli, localization of sound sources is systematically shifted to correct for the deviation of the sound from visual positions during the previous adaptation period. In the present study, this aftereffect was induced by presenting, within 17 min, 1800 repetitive noise or pure-tone bursts in combination with synchronized, and 20° disparate flashing light spots, in total darkness. Post-adaptive sound localization, measured by a method of manual pointing, was significantly shifted 2.4° (noise), 3.1° (1 kHz tones), or 5.8° (4 kHz tones) compared with the pre-adaptation condition. There was no transfer across frequencies; that is, shifts in localization were insignificant when the frequencies used for adaptation and the post-adaptation localization test were different. It is hypothesized that these aftereffects may rely on shifts in neural representations of auditory space with respect to those of visual space, induced by intersensory spatial disparity, and may thus reflect a phenomenon of neural short-term plasticity.     

Detecting structure in glass patterns: an interocular transfer study

Glass patterns are visual stimuli used here to study how local orientation signals are spatially integrated into global pattern perception. We measured a form aftereffect from adaptation to both static and dynamic Glass patterns and calculated the amount of interocular transfer to determine the binocularity of the detectors responsible for the perception of global structure. Both static and dynamic adaptation produced significant form aftereffects and showed a very high degree of interocular transfer, suggesting that Glass-pattern perception involves cortical processing beyond primary visual cortex. Surprisingly, dynamic adaptation produced significantly greater interocular transfer than static adaptation. Our results suggest a functional interaction between local orientation processing and global motion processing that contributes to form perception.     

"You talkin' to me?" Self-relevant auditory signals influence perception of gaze direction

In humans, direct gaze typically signals a deliberate attempt to communicate with an observer. An auditory signal with similar signal value is calling someone's name. We investigated whether the presence of this personally relevant signal in the auditory modality would influence perception of another individual's gaze. Participants viewed neutral faces displaying different gaze deviations while hearing someone call their own name or the name of another person. Results were consistent with our predictions, as participants judged faces with a wider range of gaze deviations as looking directly at them when they simultaneously heard their own name. The influence of this personally relevant signal was present only at ambiguous gaze deviations; thus, an overall response bias to categorize gaze as direct when hearing one's own name cannot account for the results. This study provides the first evidence that communicative intent signaled via the auditory modality influences the perception of another individual's gaze.     

Auditory motion aftereffects

Observers were adapted to simulated auditory movement produced by dynamically varying the interaural time and intensity differences of tones (500 or 2,000 Hz) presented through headphones. At lO-sec intervals during adaptation, various probe tones were presented for 1 sec (the frequency of the probe was always the same as that of the adaptation stimulus). Observers judged the direction of apparent movement (“left” or “right”) of each probe tone. At 500 Hz, with a 200-deg/sec adaptation velocity, “stationary” probe tones were consistently judged to move in the direction opposite to that of the adaptation stimulus. We call this result an auditory motion aftereffect. In slower velocity adaptation conditions, progressively less aftereffect was demonstrated. In the higher frequency condition (2,000 Hz, 200-deg/sec adaptation velocity), we found no evidence of motion aftereffect. The data are discussed in relation to the well-known visual analog-the “waterfall effect.” Although the auditory aftereffect is weaker than the visual analog, the data suggest that auditory motion perception might be mediated, as is generally believed for the visual system, by direction-specific movement analyzers.     

Congruency effects between auditory and tactile motion: Extending the phenomenon of cross-modal dynamic capture

Behavioral studies of multisensory integration in motion perception have focused on the particular case of visual and auditory signals. Here, we addressed a new case: audition and touch. In Experiment 1, we tested the effects of an apparent motion stream presented in an irrelevant modality (audition or touch) on the perception of apparent motion streams in the other modality (touch or audition, respectively). We found significant congruency effects (lower performance when the direction of motion in the irrelevant modality was incongruent with the direction of the target) for the two possible modality combinations. This congruency effect was asymmetrical, with tactile motion distractors having a stronger influence on auditory motion perception than vice versa. In Experiment 2, we used auditory motion targets and tactile motion distractors while participants adopted one of two possible postures: arms uncrossed or arms crossed. The effects of tactile motion on auditory motion judgments were replicated in the arms-uncrossed posture, but they dissipated in the arms-crossed posture. The implications of these results are discussed in light of current findings regarding the representation of tactile and auditory space.     

Motion aftereffect with subjective contours

Stationary lines appear to move from left to right following exposure to lines moving from right to left. This aftereffect, which normally is generated by exposure to moving edges that are defined in terms of local luminance discontinuity, can also be induced by adaptation to displays containing subjective contours. In both cases, stereodeficient observers demonstrated reduced interocular transfer of the aftereffect relative to stereonormal observers. Since interocular transfer of the motion aftereffect entails binocular function within the visual system, these results suggest that the perception of subjective contours depends on excitation of neural feature detectors rather than simply on cognitive inference.     

Visual body-size adaptation and estimation of tactile distance

Estimating the size of bodies is crucial for interactions with physical and social environments. Body-size perception is malleable and can be altered using visual adaptation paradigms. However, it is unclear whether such visual adaptation effects also transfer to other modalities and influence, for example, the perception of tactile distances. In this study, we employed a visual adaptation paradigm. Participants were exposed to images of expanded or contracted versions of self- or other-identity bodies. Before and after this adaptation, they were asked to manipulate the width of body stimuli to appear as ‘normal’ as possible. We replicated an effect of visual adaptation such that the body-size selected as most ‘normal’ was larger after exposure to expanded and thinner after exposure to contracted adaptation stimuli. In contrast, we did not find evidence that this adaptation effect transfers to distance estimates for paired tactile stimuli delivered to the abdomen. A Bayesian analysis showed that our data provide moderate evidence that there is no effect of visual body-size adaptation on the estimation of spatial parameters in a tactile task. This suggests that visual body-size adaptation effects do not transfer to somatosensory body-size representations.     

Simple and contingent aftereffects of perceived duration in vision and audition

After repeated presentations of a long inspection tone (800 or 1,000 msec), a test tone of intermediate duration (600 msec) appeared shorter than it would otherwise appear. A short inspection tone (200 or 400 msec) tended to increase the apparent length of the intermediate test tone. Thus, a negative aftereffect of perceived auditory duration occurred, and a similar aftereffect occurred in the visual modality. These aftereffects, each involving a single sensory dimension, aresimple aftereffects. The following procedures producedcontingent aftereffects of perceived duration. A pair of lights, the first short and the second long, was presented repeatedly during an inspection period. When a pair of test lights of intermediate duration was then presented, the first member of the pair appeared longer in relation to the second. A similar aftereffect occurred in the auditory modality. In these latter aftereffects, the perceived duration of a test light or tone is contingent—dependent—on its temporal order, first or second, within a pair of test stimuli. An experiment designed to test the possibility of cross-modal transfer of contingent aftereffects between audition and vision found no significant cross-modal aftereffects.