C1调制效应的理论评述及影响因素

C1成分是对视觉刺激最早做出反应的视皮层诱发电位,C1调制效应是指注意等因素能够影响C1振幅的现象.以往多数研究未观察到注意等因素对C1振幅的影响,仅发现注意等因素对晚于C1的P1与N1等成分存在调制作用,并有研究者据此提出延迟反馈假说.但近期研究提示,注意等因素可能会对C1成分产生影响,提示初级视皮层(V1)可能在视觉信息加工初期直接受注意调制.目前,对C1调制效应的影响因素尚未完全确定,知觉学习、负载等因素的作用尚待考察.未来研究需进一步明确C1调制效应的影响因素及实验条件.     

Asymmetry of attentional set in rhesus monkeys learning colour and shape discriminations

We trained rhesus monkeys on six visual discrimination problems using stimuli that varied in both shape and colour. For one group of animals shape was always relevant in these six problems, and colour always irrelevant, and for the other animals vice versa. During these “intradimensional shifts” (ID) the problems were learned at equal rates by the two groups, shape-relevant and colour-relevant. We then trained three further problems in which the other dimension was now relevant (“extradimensional shifts”, ED). The animals showed slower learning when shifting from colour-relevant to shape-relevant, but not when shifting from shape-relevant to colour-relevant. These results show that monkeys' ability to selectively attend to a relevant stimulus dimension and to ignore an irrelevant dimension depends on the experimenter's choice of relevant and irrelevant dimensions.     

Boundary extension: Findings and theories

A view of a scene is often remembered as containing information that might have been present just beyond the actual boundaries of that view, and this is referred to as boundary extension. Characteristics of the view (e.g., scene or nonscene; close-up or wide-angle; whether objects are cropped, static, or in motion, emotionally neutral or emotionally charged), display (e.g., aperture shape and size; target duration; retention interval; whether probes of memory involve magnification/minification or change in physical distance), and observer (e.g., allocation of attention; age; planned fixation, gaze direction, and eye movements; monocular or binocular viewing; prior exposure; neurological correlates) that influence boundary extension are reviewed. Proposed mechanisms of boundary extension (perceptual, memory, or motion schema; extension–normalization; attentional selection; errors in source monitoring) are discussed, and possible relationships of boundary extension to other cognitive processes (e.g., representational momentum; remembered distance and remembered size; amodal completion; transsaccadic memory) are briefly addressed.     

The own-age face recognition bias in children and adults

Children recognize children's faces more accurately than adult faces, and adults recognize adult faces more accurately than children's faces (e.g., Anastasi & Rhodes, 2005 Anastasi, J. S. and Rhodes, M. G. 2005. An own-age bias in face recognition for children and older adults. Psychonomic Bulletin and Review, 12: 1043–1047. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]). This is the own-age bias. Research has shown that this bias is at least partially based on experience since trainee teachers show less of an own-age bias than do other adults (Harrison & Hole, 2009 Harrison, V. and Hole, G. J. 2009. Evidence for a contact-based explanation of the own-age bias in face recognition. Psychonomic Bulletin & Review, 16: 264–269. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]). The present research tested the own-age bias in three groups of children (age 4–6, 7–9, 10–12 years) and a group of adults in the recognition of three age groups of faces (age 7–9, 20–22, and 65–90 years). Results showed an own-age bias for 7- to 9-year-old children and adults. Specifically, children could recognize faces more accurately if they were less than two years different from their own age than if they were more than two years older or younger. These results are discussed in terms of short-term experience with faces creating biases, and this rapidly changes with age.     

Gender differences on the semantic flanker task using transposed-letter target words

Previous research has demonstrated that men and women are differentially influenced by irrelevant distractors. Other lines of evidence have suggested that increasing the perceptual load of a task reduces distractor interference for participants generally. The present study examined these effects using a semantic version of the flanker task; participants made speeded responses to category target words that were flanked by irrelevant distractors. The response mapping between the target and flanker words was either congruent (mapped to the same motor response) or incongruent (target word mapped to a different motor response to that of the flankers). Target words were presented either normally (e.g., table: low perceptual load) or with the beginning letters transposed (e.g., atble: high perceptual load). The results revealed that women showed a larger congruency effect than men but this was not due to greater interference on incongruent trials. While men and women made faster responses to normal than to transposed target words, this was similar in magnitude. The magnitude of the flanker effect for normal and transposed target words was significantly correlated in men but not in women. These findings are consistent with the view that women may process target words to a deeper level than men and therefore may engage in more conflict monitoring then men.     

The effects of acute stress and perceptual load on distractor interference

Selective attention can be improved under conditions in which a high perceptual load is assumed to exhaust cognitive resources, leaving scarce resources for distractor processing. The present study examined whether perceptual load and acute stress share common attentional resources by manipulating perceptual and stress loads. Participants identified a target within an array of nontargets that were flanked by compatible or incompatible distractors. Attentional selectivity was measured by longer reaction times in response to the incompatible than to the compatible distractors. Participants in the stress group participated in a speech test that increased anxiety and threatened self-esteem. The effect of perceptual load interacted with the stress manipulation in that participants in the control group demonstrated an interference effect under the low perceptual load condition, whereas such interference disappeared under the high perceptual load condition. Importantly, the stress group showed virtually no interference under the low perceptual load condition, whereas substantial interference occurred under the high perceptual load condition. These results suggest that perceptual and stress related demands consume the same attentional resources.     

What you say matters: Exploring visual–verbal interactions in visual working memory

The aim of this study was to explore whether the content of a simple concurrent verbal load task determines the extent of its interference on memory for coloured shapes. The task consisted of remembering four visual items while repeating aloud a pair of words that varied in terms of imageability and relatedness to the task set. At test, a cue appeared that was either the colour or the shape of one of the previously seen objects, with participants required to select the object's other feature from a visual array. During encoding and retention, there were four verbal load conditions: (a) a related, shape–colour pair (from outside the experimental set, i.e., “pink square”); (b) a pair of unrelated but visually imageable, concrete, words (i.e., “big elephant”); (c) a pair of unrelated and abstract words (i.e., “critical event”); and (d) no verbal load. Results showed differential effects of these verbal load conditions. In particular, imageable words (concrete and related conditions) interfered to a greater degree than abstract words. Possible implications for how visual working memory interacts with verbal memory and long-term memory are discussed.     

Perceiving emotion from a talker: How face and voice work together

The experiment investigated how the addition of emotion information from the voice affects the identification of facial emotion. We presented whole face, upper face, and lower face displays and examined correct recognition rates and patterns of response confusions for auditory-visual (AV), auditory-only (AO), and visual-only (VO) expressive speech. Emotion recognition accuracy was superior for AV compared to unimodal presentation. The pattern of response confusions differed across the unimodal conditions and across display type. For AV presentation, a response confusion only occurred when such a confusion was present in each modality separately, thus response confusions were reduced compared to unimodal presentations. Emotion space (calculated from the confusion data) differed across display types for the VO presentations but was more similar for the AV ones indicating that the addition of the auditory information acted to harmonize the various VO response patterns. These results are discussed with respect to how bimodal emotion recognition combines auditory and visual information.     

Current versus past ambiguity in intertrial priming

Visual search is speeded when the target is repeated from trial to trial compared to when it changes, suggesting that selective attention learns from previous events. Such intertrial effects are stronger when there is more competition for selection, for example in ambiguous displays where the target is accompanied by a salient distractor. Here we investigate whether this is because the competition strengthens the learning itself, or because it allows for a learned representation to exert a greater effect. The results point to the latter. Observers looked for a colour-defined target that could repeat or change from trial to trial. A salient distractor could be present on the current trial, the previous trial, both, or neither. Intertrial effects were greater when a distractor was present on the current trial, suggesting that a primed target representation is more beneficial under conditions of competition. In contrast, distractor presence on the previous trial had no effects whatsoever, indicating that the learning process itself is not affected by competition. This suggests that the source of the learning resides at postselection stages, whereas the effects may occur at the perceptual level.     

Holistic face encoding is modulated by perceived face race: Evidence from perceptual adaptation

Human expertise at processing faces relies on how facial features are encoded: as a whole template rather than as a sum of independent features. This holistic encoding is less prominent for other-race faces, possibly accounting for the difficulty one encounters in recognizing these faces (the ‘other-race effect’). Here, we tested the hypothesis that the magnitude of holistic face encoding can be modulated by racial categorization of the face. Caucasian participants performed a face-composite task with ‘racially-ambiguous’ face-stimuli (cross-race morphed faces, equally categorized as Asian or Caucasian faces in an independent task). The perceived race of the ambiguous faces was manipulated using adaptation. Experiment 1 showed that identical morphed face-stimuli were processed more holistically when perceived as ‘same-race’ than as ‘other-race’, i.e., following adaptation to ‘other-race’ versus ‘same-race’, respectively. Experiment 2 ascertained that the determining factor in the observed holistic processing modulation was the race of the racially-ambiguous face as perceived, rather than expected, by the participants, which supports the idea that the holistic processing of the face-stimuli was modulated by their race-categorization at the perceptual level.