Fear selectively modulates visual mental imagery and visual perception

Preferences for faces are thought to be the result of either general adaptations for mate selection, and thus influenced by sexual dimorphism, or mechanisms of general information processing and thus nonspecific to faces. If mate choice determines face preference then it should follow that the sex of a face should affect attractiveness judgements. To test this idea we used image morphing to generate three versions of face images: original, opposite sex, and antiface. First we established that the sex of the face was identifiable in our images. We then collected attractiveness ratings for the three face types. We found that attractiveness ratings to the original faces were correlated with, and did not differ significantly between, ratings to the opposite-sex faces. However, ratings for either the original or opposite face types were not correlated with and were significantly lower than ratings to the antifaces. Our findings failed to support the idea that attractiveness is related to sexual dimorphism in faces alone but suggest instead that other more generic factors influence preferences for all faces.     

Eye movements during visual mental imagery

It has long been debated whether eye movements play a functional role in visual mental imagery. A recent paper by Laeng and Teodorescu presents new evidence that eye movements are stored as a spatial index that is used to arrange the component parts correctly when mental images are generated.     

Age differences in the relationship between visual movement imagery and performance on kinesthetic acuity tests

The Vividness of Movement Imagery Questionnaire was administered to 280 fourteen-year-olds and 186 ten-year-olds, who were then tested on measures of kinesthetic acuity. The relationship between visual movement imagery and kinesthetic acuity scores was significant in the older group: Those with high levels of visual movement imagery performed significantly better on measures of kinesthetic acuity than did those with low imagery. No such effect was found in the younger group. The results indicate that for adolescents, the confounding effect of visual imagery affects the researcher's ability to interpret kinesthetic acuity scores. The relationship between imagery and kinesthesis appears to develop over the period between 10 and 14 years, although such an interpretation may be premature because the measurement of visual movement imagery in the younger age group is problematic.     

Explorations of creative visual synthesis in mental imagery

The mental synthesis of visual patterns has been previously studied by instructing subjects to imagine assembling the component parts in specific ways. We report two experiments that show that subjects can often discover recognizable patterns in imagery when the component parts are randomly chosen and are provided without instructions for how they might be assembled. On each trial, the subjects were given a set of three parts, consisting of geometric forms, lines, or alphanumeric characters, and were instructed to close their eyes and imagine combining the parts to make some type of recognizable pattern. They were successful in doing so on about 40 % of the trials. Many of these mentally synthesized patterns were strikingly creative, and few of them could be predicted, either by the experimenter or by the subjects themselves, simply by knowing what the parts were. On the contrary, most of the subjects reported that they had performed the task by imagining various combinations of the parts until a recognizable pattern “emerged.” These findings show that visual discoveries in imagery can be reliably induced under appropriate laboratory conditions.     

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.     

Central visual persistences: I. Visual and kinesthetic interactions

Phenomena associated with 'central visual persistences' (CPs) are new to both medical and psychological literature. Five subjects have reported similar CPs: positive afterimages following brief fixation of high-contrast objects or drawings and eye closure. CPs duplicate shapes and colors of single objects, lasting for about 15 s. Unlike retinal afterimages, CPs do not move with the eyes but are stable in extrapersonal space during head or body rotations. CPs may reflect sustained neural activity in neurons of association cortex, which mediate object perception. A remarkable finding is that CPs can be moved in any direction by the (unseen) hand holding the original seen object. Moreover, a CP once formed will 'jump' into an extended hand and 'stick' in that hand as it moves about. The apparent size of a CP of a single object is determined by the size of the gap between finger and thumb, even when no object is touched. These CPs can be either magnified or minified via the grip of the extended hand. The felt orientation of the hand-held object will also determine the orientation of the CP seen in that hand. Thus, kinesthetic signals from hand and arm movements can determine perceived location, size, and orientation of CPs. A neural model based on physiological studies of premotor, temporal, parietal, and prefrontal cortices is proposed to account for these novel phenomena.     

Visual dominance in the cross-modal kinesthetic to kinesthetic plus visual feedback condition

In previous studies subjects who have learned a positioning response with kinesthetic feedback tended to make greater errors when visual feedback was provided during later trials. These subjects have always performed with both kinesthetic and visual feedback available. This study determined whether subjects with only visual feedback would produce errors similar to those who received kinesthetic plus visual feedback. Blindfolded subjects learned to move a handle to a criterion location with knowledge of results following each trial. Subjects then were assigned to one of three experimental groups, with only kinesthetic feedback, with kinesthetic plus visual feedback, or with only visual feedback. Subjects had 9 trials without knowledge of results in these feedback conditions. When visual feedback was available, subjects tended to make longer response errors. This finding replicates previous studies. Also, the similarity of performances from the conditions with visual feedback indicated the dominance of visual information in the condition with kinesthetic plus visual feedback.     

视觉表象个体差异及其神经基础

视觉表象涉及人类一种重要信息表征方式, 与工作记忆和注意相比, 视觉表象研究更为关注其所产生的主观内容, 而这一主观内容的产生存在明显的个体差异。本文从个体差异的角度, 系统介绍了视觉表象个体差异的表现与内在的神经基础及其可能的应用, 并展望了未来的研究方向。本研究将有助于对视觉表象个体差异的认识, 促进视觉表象功能与实质问题研究的进一步开展。     

Age differences in visual and kinesthetic short-term memory

30 elderly subjects were matched with 30 young subjects and tested on a kinesthetic short-term memory task which required the replication of criterion moves after a variable retention interval under conditions of either rest, differing interpolated movement tasks, or mental activity. A visual control condition was used. Differing interference and temporal decrements were observed. Both old and young subjects differed significantly between sighted and blindfold conditions; however, there was no difference between the performance of the old and the young in the blindfold (kinesthetic) condition. These findings were discussed with respect to practical implications for the retraining of old subjects on certain motor tasks.     

Effects of depression on sensory/motor vs. central processing in visual mental imagery

Actual anger response styles during anger encounters may well diverge from self-reported habitual anger response styles, such as anger - in, anger - out, or anger control. Also, the relationship of actual anger response styles to broad personality traits is not well known. We obtained anger self - reports, physiological reactivity (diastolic blood pressure, skin temperature at the forehead, and EMG extensor digitorum), and ratings of facial anger expression, and defined actual anger response style dimensions of “intensity”, “suppression”, “repression”, and “denial” as particular patterns of discrepancies among these responses. A total of 80 female subjects were randomly assigned to a treatment (Tr) and a control (Co) group. Anger was induced through real - life provocations. Compared to Co, Tr subjects showed larger physiological responses and reported more anger. Habitual anger response styles did not predict actual styles, whereas extraversion and neuroticism did. Control subjects scoring low on extraversion or high on neuroticism reacted with high denial, that is, with stronger physiological and behavioural than experiential anger, whereas the opposite pattern of low denial was found for treatment subjects low on extraversion or high on neuroticism. These results suggest that both the particular situation and broad but not narrow personality traits exert an influence on actual anger response styles.     

Visual versus kinesthetic mental imagery: Efficacy for the retention and transfer of a closed motor skill in young children

The main purposes of this study were (a) to compare the effects of mental imagery combined with physical practise and specific physical practise on the retention and transfer of a closed motor skill in young children; (b) to determine the mental imagery (visual vs. kinesthetic), which is the most efficient for retention and transfer of a closed motor skill; and (c) to verify the relationship between movement image vividness and motor performance. As for the secondary purpose, it was to compare the effects of gender on motor learning. Participants (n = 96) were selected from 3 primary schools. These participants were divided into 6 groups and submitted to different experimental conditions. The experimental task required the participants to throw, with the nondominant hand (left hand), a ball toward a target composed of 3 concentric circles. The results demonstrated that performance obtained by the mental imagery (visual or kinesthetic) combined with physical practise group was, during the retention phase, equivalent to that produced by the specific physical practise group but significantly superior during the transfer of closed motor skill. These results showed the potential benefits of mental imagery as a retention strategy intended for motor skills and performance enhancement. Such results could be explained by the similarity of 3 principal functional evidences shared by mental and physical practise: behavioural, central, and peripheral (as suggested by Holmes & Collins, 2001). (PsycINFO Database Record (c) 2008 APA, all rights reserved).     

Scrutinizing visual images: The role of gaze in mental imagery and memory

Gaze was monitored by use of an infrared remote eye-tracker during perception and imagery of geometric forms and figures of animals. Based on the idea that gaze prioritizes locations where features with high information content are visible, we hypothesized that eye fixations should focus on regions that contain one or more local features that are relevant for object recognition. Most importantly, we predicted that when observers looked at an empty screen and at the same time generated a detailed visual image of what they had previously seen, their gaze would probabilistically dwell within regions corresponding to the original positions of salient features or parts. Correlation analyses showed positive relations between gaze’s dwell time within locations visited during perception and those in which gaze dwelled during the imagery generation task. Moreover, the more faithful an observer’s gaze enactment, the more accurate was the observer’s memory, in a separate test, of the dimension or size in which the forms had been perceived. In another experiment, observers saw a series of pictures of animals and were requested to memorize them. They were then asked later, in a recall phase, to answer a question about a property of one of the encoded forms; it was found that, when retrieving from long-term memory a previously seen picture, gaze returned to the location of the part probed by the question. In another experimental condition, the observers were asked to maintain fixation away from the original location of the shape while thinking about the answer, so as to interfere with the gaze enactment process; such a manipulation resulted in measurable costs in the quality of memory. We conclude that the generation of mental images relies upon a process of enactment of gaze that can be beneficial to visual memory.     

Visual mental imagery and visual perception: Structural equivalence revealed by scanning processes

The research reported in the present article investigates whether information is represented the same way in both visual mental imagery and the early phases of visual perception. In Experiment 1, the same participants scanned over patterns of dots in a mental image (with images based on a just-seen pattern), during perception, and in an iconic image. The time to scan increasing distances increased at comparable rates in the three tasks. However, in Experiment 2, when mental images were created from information stored in long-term memory, participants scanned more slowly in the mental image condition. Nevertheless, the rates of scanning in the perceptual tasks were highly correlated with the rates of scanning in the imagery tasks in both experiments. The results provide evidence that mental images and perceived stimuli are represented similarly and can be processed in the same way.     

Visual perception and visual mental imagery of emotional faces generate similar expression aftereffects

What is the relationship between visual perception and visual mental imagery of emotional faces? We investigated this question using a within-emotion perceptual adaptation paradigm in which adaptation to a strong version of an expression was paired with a test face displaying a weak version of the same emotion category. We predicted that within-emotion adaptation to perception and imagery of expressions would generate similar aftereffects, biasing perception of weak emotional test faces toward a more neutral value. Our findings confirmed this prediction. Adaptation to mental images yielded aftereffects that inhibited emotion recognition of test expressions, as participants were less accurate at recognising these stimuli compared to baseline. While the same inhibitory effect was observed when expressions were visually perceived, the size of the aftereffects was greater for perception than imagery. These findings suggest the existence of expression-selective neural mechanisms that subserve both visual perception and visual mental imagery of emotional faces.     

Self-rated imagery and encoding strategies in visual memory.

The value of self-rated vividness of imagery in predicting performance was investigated, taking into account the mnemonic strategies utilized among subjects performing a visual-memory task. Subjects classified as 'good' or 'poor' imagers, according to their scores in the Vividness of Visual Imagery Questionnaire (VVIQ; Marks, 1972), were to detect as rapidly as possible differences between pairs of similar pictures presented consecutively. No coding instructions were given and the mnemonic strategies used were analysed by studying subjective reports and objective performance measurements. The results indicated that the subjects utilized two main strategies--a detail or an image strategy. The detail strategy was the more efficient. In accordance with a previous study (Berger & Gaunitz, 1977), it was found that the VVIQ did not discriminate between performance by 'good' and 'poor' imagers. However, among subjects who used the image strategy, 'good' imagers performed more rapidly than 'poor' imagers. Self-rated imagery may then have some value in predicting performance among individuals shown to have utilized an image strategy.     

Picture yourself at the polls: visual perspective in mental imagery affects self-perception and behavior

The present research demonstrates that the visual perspective--own first-person versus observer's third-person--people use to picture themselves engaging in a potential future action affects their self-perceptions and subsequent behavior. On the eve of the 2004 U.S. presidential election, registered voters in Ohio were instructed to use either the first-person or the third-person perspective to picture themselves voting in the election. Picturing voting from the third-person perspective caused subjects to adopt a stronger pro-voting mind-set correspondent with the imagined behavior. Further, this effect on self-perception carried over to behavior, causing subjects who were instructed to picture voting from the third-person perspective to be significantly more likely to vote in the election. These findings extend previous research in autobiographical memory and social judgment linking the observer's perspective with dispositional attributions, and demonstrate the causal role of imagery in determining future behavior.     

Representations in mental imagery and working memory: Evidence from different types of visual masks

Although few studies have systematically investigated the relationship between visual mental imagery and visual working memory, work on the effects of passive visual interference has generally demonstrated a dissociation between the two functions. In four experiments, we investigated a possible commonality between the two functions: We asked whether both rely on depictive representations. Participants judged the visual properties of letters using visual mental images or pictures of unfamiliar letters stored in short-term memory. Participants performed both tasks with two different types of interference: sequences of unstructured visual masks (consisting of randomly changing white and black dots) or sequences of structured visual masks (consisting of fragments of letters). The structured visual noise contained elements of depictive representations (i.e., shape fragments arrayed in space), and hence should interfere with stored depictive representations; the unstructured visual noise did not contain such elements, and thus should not interfere as much with such stored representations. Participants did in fact make more errors in both tasks with sequences of structured visual masks. Various controls converged in demonstrating that in both tasks participants used representations that depicted the shapes of the letters. These findings not only constrain theories of visual mental imagery and visual working memory, but also have direct implications for why some studies have failed to find that dynamic visual noise interferes with visual working memory.