Common neural systems associated with the recognition of famous faces and names: An event-related fMRI study

Person recognition can be accomplished through several modalities (face, name, voice). Lesion, neurophysiology and neuroimaging studies have been conducted in an attempt to determine the similarities and differences in the neural networks associated with person identity via different modality inputs. The current study used event-related functional-MRI in 17 healthy participants to directly compare activation in response to randomly presented famous and non-famous names and faces (25 stimuli in each of the four categories). Findings indicated distinct areas of activation that differed for faces and names in regions typically associated with pre-semantic perceptual processes. In contrast, overlapping brain regions were activated in areas associated with the retrieval of biographical knowledge and associated social affective features. Specifically, activation for famous faces was primarily right lateralized and famous names were left-lateralized. However, for both stimuli, similar areas of bilateral activity were observed in the early phases of perceptual processing. Activation for fame, irrespective of stimulus modality, activated an extensive left hemisphere network, with bilateral activity observed in the hippocampi, posterior cingulate, and middle temporal gyri. Findings are discussed within the framework of recent proposals concerning the neural network of person identification.     

Attentional mechanisms associated with repressive distancing

This research explores the role of attentional shift and disengagement in repressive distancing. During a target-detection task in which emotional and neutral facial expressions were used as cues, participants received performance feedback intended to elicit a negative emotional reaction that rendered the task either threatening or not threatening to self-concept. When the task was perceived to threaten self-concept, repressors distanced themselves by rapidly disengaging their attention from the facial expressions rather than by slowly shifting or not shifting their attention to the facial expressions. Attentional disengagement was accompanied by sympathetic nervous system activity suggestive of a defense response. This research provides further insight into the nature and consequences of the interplay of dispositional tendencies, situational contexts, and higher order cognitive influences in attentional behavior.     

暴食症的影响因素及其机制

暴食症表现为反复发作的暴饮暴食症状, 并伴随着强烈的沮丧感, 个体在进食时通常感觉失去控制, 进食大量食物。暴食行为受到应激、负性情绪、冲动性人格、身体不满意与限制性进食以及父母的喂养方式影响。关于暴食症发生和维持的理论模型主要有情感调节理论、食物成瘾模型、人际关系模型以及完美主义模型。未来要进一步探究影响暴食的因素, 完善暴食症的理论模型, 运用脑成像等技术深入研究暴食症的认知神经机制并加强对暴食症的干预与治疗研究。     

How evolutionary history shapes recognition mechanisms

Evolutionary psychologists have emphasized the importance of natural selection in shaping cognitive functions, but historical contingency has not received direct study. This is crucial because in response to selection, complex traits tend to be fine-tuned or jury-rigged rather than totally reconstructed. We hypothesize that the neural and cognitive strategies an animal employs in signal recognition are influenced by the strategies used by its ancestors. The responses of female túngara frogs to ancestral calls and to calls of other closely related species are influenced by history. By training artificial neural networks with a series of calls that mimic the species' past history of call evolution or various control histories, we have shown that only networks that evolved through the mimetic history predict the response biases of túngara frogs.     

手写体文字识别的特点及神经机制

手写体文字与打印体文字的识别过程存在很大差异, 与打印体文字相比, 手写体文字的识别受文本材料的影响更大, 具体包括文字的物理结构特性、文字特性、书写风格等。有关神经机制的研究发现, 手写体文字识别加工所涉及的脑区与打印体文字有所区别, 它既包含识别打印体文字的枕叶和外侧额顶叶, 还涉及到手写体文字识别的文化特异性脑区, 包括左后侧运动皮层, 外侧前额叶和后侧顶叶皮层。手写体文字加工既涉及整体加工, 也涉及特征加工, 加工方式既有其特异性, 又有与打印体文字的共同之处。未来研究应该进一步探究大脑在识别手写体文字时, 怎样在嘈杂的视觉信息中提取目标词, 并考虑手写体文字识别理论模型的构建, 以便更好地解释手写体文字的识别过程。     

Simple lines and shapes are associated with,and communicate,distinct emotions

We investigated whether lines and shapes that present face-like features would be associated with emotions. In Experiment 1, participants associated concave, convex, or straight lines with the words happy or sad. Participants found it easiest to associate the concave line with happy and the convex line with sad. In Experiment 2, participants rated (valence, pleasantness, liking, and tension) and categorised (valence and emotion words) two convex and concave lines that were paired with six distinct pairs of eyes. The presence of eyes affected participants’ valence ratings and response latencies; more congruent eye–mouth matches produced more consistent ratings and faster reaction times. In Experiment 3, we examined whether dots that resembled eyes would be associated with emotional words. Participants found it easier to match certain sets of dots with specific emotions. These results suggest that facial gestures that are associated with specific emotions can be captured using relatively simple shapes and lines.     

Common mechanisms in error monitoring and action effect monitoring

In the present study, we considered error-related brain activity in event-related potentials, to investigate the relationship between error monitoring—that is, the detection and evaluation of erroneous responses—and action effect monitoring—that is, monitoring of the sensory consequences of behavior. To this end, participants worked on a task-switching paradigm that consisted of a free-choice task, in which a puzzle piece had to be attached to an existing one (the prime task), and a subsequent color flanker task (the probe task). We examined whether unexpected action effects in the prime task would affect the subsequent error monitoring in the probe task. We found the neural correlates of error monitoring during the probe task, the error-related negativity as well as the error positivity, to be increased after unexpected action effects in the prime task. In contrast, the neural correlates of visual attention were decreased after unexpected action effects, in line with recent findings on an attenuation of sensory processing after errors. Our results demonstrate a direct link between monitoring processes in the two tasks. We propose that both error monitoring and action effect monitoring rely on a common generic monitoring system related to novelty detection or affective processing. Preactivating this system by means of unexpected action effects increases the sensitivity for detecting an error in the subsequent task.     

Brain rCBF and performance in visual imagery tasks: Common and distinct processes

The present study was designed to discover whether variations in normalised regional cerebral blood flow (rCBF) in different brain areas predict variations in performance of different imagery tasks. Positron emission tomography (PET) was used to assess brain activity as 16 participants performed four imagery tasks. These tasks were designed so that performance was particularly sensitive to the participant's ability to form images with high resolution, to generate images from distinct segments, to parse imaged forms into parts while inspecting them, or to transform (rotate) images. Response times and error rates were recorded. Multiple regression analyses revealed that variations in most brain areas predicted variations in performance of only one task, thus demonstrating that the four tasks tap largely independent imagery processes. However, we also found that some underlying processes were recruited by more than one task, particularly those implemented in the occipito‐parietal sulcus, the medial frontal cortex, and Area 18.     

Common and distinct patterns of affective response in dimensions of anxiety and depression

The authors examined the time course of affective responding associated with different affective dimensions--anxious apprehension, anxious arousal, and anhedonic depression--using an emotion-modulated startle paradigm. Participants high on 1 of these 3 dimensions and nonsymptomatic control participants viewed a series of affective pictures with acoustic startle probes presented before, during, and after the stimuli. All groups exhibited startle potentiation during unpleasant pictures and in anticipation of both pleasant and unpleasant pictures. Compared with control participants, symptomatic participants exhibited sustained potentiation following the offset of unpleasant stimuli and a lack of blink attenuation during and following pleasant stimuli. Common and unique patterns of affective responses in the 3 types of mood symptoms are discussed.     

Cortical regions associated with different aspects of object recognition performance

In the present object recognition study, we examined the relationship between brain activation and four behavioral measures: error rate, reaction time, observer sensitivity, and response bias. Subjects perceptually matched object pairs in which structural similarity (SS), an index of structural differentiation, and exposure duration (DUR), an index of task difficulty, were manipulated. The SS manipulation affected the fMRI signal in the left anterior fusiform and parietal cortices, which in turn reflected a bias to respond same. Conversely, an SS-modulated fMRI signal in the right middle frontal gyrus reflected a bias to respond different. The DUR manipulation affected the fMRI signal in occipital and posterior fusiform regions, which in turn reflected greater sensitivity, longer reaction times, and greater accuracy. These findings demonstrate that the regions most strongly implicated in processing object shape (SS-modulated regions) are associated with response bias, whereas regions that are not directly involved in shape processing are associated with successful recognition performance.     

Detection and criterion change associated with different test contexts in recognition memory

Three groups of physics Ss and three groups of arts Ss viewed 20 physics words (PWs) and 20 common words (CWs) in a randomly ordered inspection sequence. Ss were then assigned to one of three recognition test conditions where the inspection items were embedded in different sequences of 120 additional words (60 PWs + 60 CWs; 100 PWs + 20 CWs, 20 pWs + 100 CWs). Signal-detection and Luce analyses examined the effects of the different test contexts on Ss′ true sensitivity and response bias. While all Ss found detection of PWs easier than CWs, these judgments varied according to the properties of the recognition sequences. This latter finding was interpreted as indicating that Ss adopted a conservative and probabilistic strategy for the recognition task as a whole rather than utilizing different strategies for PWs and the CWs where these would result in superior overall performance.     

Common mechanisms in apparent motion perception and visual pattern matching

There are close functional similarities between apparent motion perception and visual pattern matching. In particular, striking functional similarities have been demonstrated between perception of rigid objects in apparent motion and purely mental transformations of visual size and orientation used in comparisons of objects with respect to shape but regardless of size and orientation. In both cases, psychophysical data suggest that differences in visual size are resolved as differences in depth, such that transformation of size is done by translation in depth. Furthermore, the process of perceived or imagined translation appears to be stepwise additive such that a translation over a long distance consists of a sequence of smaller translations, the durations of these steps being additive. Both perceived and imagined rotation also appear to be stepwise additive, and combined transformations of size and orientation appear to be done by alternation of small steps of pure translation and small steps of pure rotation. The functional similarities suggest that common mechanisms underlie perception of apparent motion and purely mental transformations. In line with this suggestion, functional brain imaging has isolated neural structures in motion area MT used in mental transformation of size.     

Phonological underspecification and mapping mechanisms in the speech recognition lexicon

The problem of recognizing phonological variations in the speech input has triggered numerous treatments in speech processing models. Two areas of current controversy are the possibility of phonological underspecification in the mental lexicon and the nature of the mapping mechanism from the speech signal to the abstract lexical entry. We present data from cross-modal repetition priming experiments in English designed to test the differing predictions of speech recognition models regarding tolerance of phonological mismatch in speech. The results show effects of underspecification, supporting models using underspecified lexical entries (e.g. Lahiri & Marslen-Wilson, 1991; Reetz & Lahiri, 2001) over those using fully specified lexical entries (e.g., McClelland & Elman, 1986). The results also show no effects of context, thus favoring context-independent mapping, such as that in the three-way matching mechanism of the Lahiri and Reetz FUL model ( Lahiri, 1999; Reetz, 1998 and Reetz, 1999; Reetz & Lahiri, 2001) over context-dependent mapping used in phonological inference rules ( Gaskell and Marslen-Wilson, 1996 and Gaskell and Marslen-Wilson, 1998).     

Process demands of rejection mechanisms of recognition memory

A surge of research has been conducted to examine memory editing mechanisms that help distinguish accurate from inaccurate memories. In the present experiment, the authors examined the ability of participants to use novelty detection, recollection rejection, and plausibility judgments to reject lures presented on a recognition memory test. Participants studied a list of word pairs that were arranged in a category relationship (both words from the same category) or an unrelated relationship (both words from different categories) under full or divided attention. At test, participants were given a yes/no recognition test in which they were to respond after seeing the test items for 400 ms or 2,800 ms. Some of the test items were rearranged word pairs that were consistent with the study relationship, whereas others were inconsistent with the study relationship. The results demonstrate that the participants required full attention at study to use novelty detection, recollection rejection, and plausibility judgments to reject lures. Moreover, the results indicate that a long response deadline at test was needed for participants to use both recollection rejection and plausibility judgments to reject lures.     

Possible olfaction-based mechanisms in human kin recognition and inbreeding avoidance

Three studies explored kin recognition through olfaction. In Study I, adults (N=22) were tested for ability to identify the odors of themselves; their mother; their father; a sister; a brother; a familiar, unrelated individual; and a stranger. Acquaintances were identified as accurately as biological kin, implicating an association mechanism. However, biological kin were often confused, implicating phenotypic matching. Same-sex kin were confused more than opposite-sex kin, but mainly when same-sex kin had odors of similar intensity. Study II implicated phenotypic matching. Mothers (N=18) could identify their biological children but not their stepchildren. The preadolescent children (N=37) identified their full siblings but not half-siblings or stepsiblings. Thus, olfactory cues may help mediate favoritism of blood relatives. In Study III, mutual olfactory aversion occurred only in the father-daughter and brother-sister nuclear family relationships. Recognition occurred between opposite-sex siblings but not same-sex siblings. Thus, olfaction may help mediate the development of incest avoidance during childhood (the Westermarck effect).     

Shifting visual attention and selecting motor responses: distinct attentional mechanisms.

Does shifting visual attention require the same central mechanism as that required for selecting overt motor responses? In Experiment 1, Ss performed 2 tasks: a speeded manual response to a tone and an unspeeded report of a cued target letter in a brief masked array. Stimulus onset asynchrony (SOA) between tone and array was varied. If the attention shift to the target was delayed by the first task, then there should be more second-task errors at short SOAs and on trials with slow first-task responses. In fact, SOA effects and dependencies were minimal. Results were unchanged in further experiments in which the relation between cue and target was symbolic, spatially "unnatural," or based on the color of the target. Two additional experiments validated key assumptions of the method. The results confirm that although selection of motor responses constitutes a processing bottleneck, the control of visual attention operates independently of this bottleneck.