The functional equivalence of mental images and errors of movement.

Four experiments are reported demonstrating that mental images are functionally equivalent to physical errors of movement in producing changes in visual-motor coordination, at both central and peripheral levels of the visual-motor system. In the first experiment, subjects in one condition pointed at a target seen through laterally displacing prisms and were instructed to imagine pointing errors identical to those recorded previously for subjects in a separate condition who actually observed their pointing errors. Changes in pointing accuracy during adaptation procedures and visual-motor aftereffects following these procedures for subjects who imagined their errors were proportional to visual-motor shifts and aftereffects for subjects who observed their errors. In the second experiment, these same imagery instructions resulted in identical pointing shifts and aftereffects even in the case where prisms did not displace the target. The third experiment showed that when subjects believe that their mental images of pointing errors do not correspond to their actual pointing errors, pointing aftereffects result that are characteristic of the processing of error information at peripheral, but not central, levels of the visual motor system. The final experiment showed that when subjects do believe that their images of pointing errors correspond to actual pointing errors, but imagine the pointing movement itself in addition to their errors, pointing aftereffects result that are characteristic of the processing of error information at central, but not peripheral, levels of the visual-motor system. Contributions to visual-motor aftereffects from these two levels appear to be additive. Another significant result was that, in the imagery feedback conditions of each experiment, subjects who gave high ratings of vividness to their mental imagery showed the greatest magnitude of pointing aftereffects. These findings establish that mental images for errors of movement can produce stable visual-motor changes that cannot be accounted for simply by subjects' expectations regarding the actual consequences of their actions.     

The horizon-ratio relation as information for relative size in pictures

The horizon-ratio relation was found to be an effective source of information for relative size in pictures under some conditions: when the difference in image size of depicted “same real size” objects was not too great (Experiment 1), and when the horizon line was not too high or too low in the picture (Experiment 2). The latter finding seemed to be linked to the observers’ identification of the horizontal line as the horizon (and not as the edge of a finite surface). In addition, individual patterns of response were remarkably systematic even in the absence of a horizon, or any other pictorial information, (Experiment 3). It is suggested that in this case observers imposed a horizon on the picture on which to base their relative size judgments, possibly based on the observer’s own eye level or on the content of the picture. It is concluded that although the horizon-ratio relation provides the same kind of information as that available in the optic arrays from real scenes, pictorial information requires the satisfaction of additional constraints in order to be fully effective.     

Manipulation of visual mental images in children and adults.

Recently, there has been a debate on whether visual patterns can be transformed and reinterpreted in mental imagery. In the present study, task demands and age of subjects were manipulated to see whether children and adults were able to discover a novel visual pattern after transforming a mental image. Two tasks, called combination and subtraction, were devised. They consist of either compounding or taking away parts of images to discover a new construal. Results indicate that not only adults, but also children aged 6 and 10, are able to transform a mental image so as to yield another image with a different interpretation. Task demands had a greater effect on children than adults, consistent with the suggestion that the ease of manipulating mental images is a function of the efficiency of control processes.     

Processing global information in briefly presented pictures

Summary The effect on object recognition of the processing of the global information in contextually coherent scenes was investigated in two experiments. In Experiment 1 subjects saw 100 ms presentations of line drawings containing objects that were either usual or unusual given the picture context. Following each exposure they were required to select from among four objects the one that had been contained in the scene. The consistency of the three distractor alternatives with the meaning of the picture was varied. Recognition accuracy was poor for unusual objects and when the distractors were consistent with the picture meaning and did not substantially differ from the performance of subjects who selected response alternatives after being provided with a theme of the picture, without actually viewing the pictures. This supports the conclusion that subjects were responding on the basis of the global information but not the local object information in the pictures. When the exposure duration was increased to 2 s (Experiment 2), processing of local information was apparent for both usual and unusual objects but effects of the global information were still evident.     

Spatial information with pictures and words in visual short-term memory

In a delayed matching task, the influence of spatial congruence between study and test on visual short-term memory for geometric figures and words was investigated. Subjects processed series of pictures which showed three words or three geometric figures arranged as rows or as triangular configurations. At test, the elements were presented in the identical or in the alternative configuration as at study. In the non-matching case, one of the studied elements was exchanged. The delay was 5 s. Subjects judged whether the elements were the same as during study, independent of their configuration. In Exp. 1, pictures of figures and words were mixed within one list. For both modalities, the response times were longer if the configuration at test was incongruent to the one at study. This contradicts the results of Santa, who observed effects of spatial congruency for figures, but not for words. In Exp. 2 we therefore presented the same material as in Exp. 1, but now the lists were modality-pure, as in the experiment of Santa – i.e., words and figures were shown in different lists. This time, spatial incongruency impaired recognition of the figures, but not recognition of the words. These results show that in a non-verbal context, isolated visually presented words are spatially encoded as non-verbal stimuli (figures) are. However, the word stimuli are encoded differently if the task is a pure verbal one. In the latter case, spatial information is discarded. Received: 9 September 1997 / Accepted: 30 March 1998     

Recognition rights,mental health consumers and reconstructive cultural semantics

Introduction  

Those in mental health-related consumer movements have made clear their demands for humane treatment and basic civil rights, an end to stigma and discrimination, and a chance to participate in their own recovery. But theorizing about the politics of recognition, 'recognition rights' and epistemic justice, suggests that they also have a stake in the broad cultural meanings associated with conceptions of mental health and illness.     

Electrophysiological differences in the processing of affective information in words and pictures

It is generally assumed that affective picture viewing is related to higher levels of physiological arousal than is the reading of emotional words. However, this assertion is based mainly on studies in which the processing of either words or pictures has been investigated under heterogenic conditions. Positive, negative, relaxing, neutral, and background (stimulus fragments) words and pictures were presented to subjects in two experiments under equivalent experimental conditions. In Experiment 1, neutral words elicited an enhanced late positive component (LPC) that was associated with an increased difficulty in discriminating neutral from background stimuli. In Experiment 2, high-arousing pictures elicited an enhanced early negativity and LPC that were related to a facilitated processing for these stimuli. Thus, it seems that under some circumstances, the processing of affective information captures attention only with more biologically relevant stimuli. Also, these data might be better interpreted on the basis of those models that postulate a different access to affective information for words and pictures.     

Age-related deficits in generation and manipulation of mental images: II. The role of dorsolateral prefrontal cortex.

The authors investigated neural substrates of age-related declines in mental imagery. Healthy adult participants (ages 19 to 77) performed a series of visual-spatial mental imagery tasks that varied in apparent difficulty and involved stimuli of varying graphic complexity. The volumes of the dorsolateral frontal cortex (DLPFC) and posterior visual processing areas were estimated from magnetic resonance imaging scans. The volume of the DLPFC and the fusiform cortex, working-memory capacity, and performance on the tasks involving image generation and manipulation were significantly reduced with age. Further analyses suggested that age-related deficits in performance on mental imagery tasks may stem in part from age-related shrinkage of the prefrontal cortex and age-related declines in working memory but not from age-related slowing of sensorimotor reaction time. The volume of cortical regions associated with modality-specific visual information processing did not show a consistent relationship with specific mental imagery processes.     

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.     

Measuring the size of mental images

Mental images seem to have a size; the experimental problem was to map that image size onto a scale of physical measurement. To this end, two experiments were conducted to measure the size of mental images in degrees of visual angle. In Experiment 1, college students employed light pointers to indicate the horizontal extent of projected mental images of words (the letter string, not the referent). Imagined words covered about 1.0 degress of visual angle per letter. In Experiment 2, a more objective eye-movement response was used to measure the visual angle size of imagined letter strings. Visual angle of eye movement was found to increase regularly as the letter distance between the fixation point and a probed letter position increased. Each letter occupied about 2.5 degrees of visual angle for the four-letter strings in the control/default size condition. Possible relations between eye movements and images are discussed.     

Frames and images: sequential effects in mental rotation

Recent studies have shown that response time in mental rotation increases with the angular deviation between the current and preceding stimuli, suggesting a frame rotation process in which the intrinsic frame of the previous stimulus is brought into congruence with the coordinates of the current stimulus. In contrast, we show that this process involves image rotation in which the present stimulus is brought into alignment with the orientation of the previous stimulus. Such "backward alignment" succeeds only for shape-preserving sequences (i.e., identical stimuli at different orientations). Four experiments show that the backward alignment process (a) competes with the uprighting process typically found in mental rotation, and the response is determined by the process requiring the shortest rotational path; (b) is related to the tendency to repeat the previous response; (c) is insensitive to the position of the vertical; (d) is indifferent to the representation of the stimulus in long term memory; and (e) is different from the process underlying preparation for a stimulus in a specified orientation.     

Age-related deficits in generation and manipulation of mental images: I. The role of sensorimotor speed and working memory.

The authors investigated age-related slowing of information processing in mental imagery tasks. Eighty-five healthy adults (ages 18 to 77) performed a visual, sensorimotor, reaction-time task; a visual-perceptual choice reaction task; and 3 mental imagery tasks that varied in apparent difficulty and involved stimuli at 2 levels of graphic complexity. Age was associated with prolongation of response time across all tasks and both levels of stimulus complexity. Accuracy of response was adversely affected by increase in stimulus complexity in all tasks, whereas it was negatively related to age only on the tasks with substantial mental imagery requirements. Slowing of information processing and reduction in accuracy were mediated by declines in working memory but not by decrease of sensorimotor speed.     

The fading of stabilized images: Eye movements and information processing

Two experiments are reported which indicate that neural and photochemical satiation processes are inadequate to explain the fading of the stabilized retinal image. When eye movements are attempted over the stimulus, fading occurs more rapidly, indicating an information processing component in the disappearance of the image.     

Dissociation between the mental rotation of visual images and motor images in unilateral brain-damaged patients

Deficits in the mental rotation of body parts and of external objects can be doubly dissociated (Rumiati, Tomasino, Vorano, Umiltà, & De Luce, 2001; Sirigu & Duhamel, 2001; Tomasino, Rumiati, & Umità, in press). The aim of this study was to replicate this finding and to then investigate the relevance of the specific hemispheres in these deficits. Nine patients with unilateral lesions (five in the Left Hemisphere and four in the Right) and 20 control subjects, performed a single task requiring mental rotation of hands, and two tasks requiring mental rotation of external objects. RH patients were impaired in the rotation of external objects, but showed intact performance on the rotation of hands; the opposite pattern was found for LH patients. These results support the view that the LH contributes to the mental rotation of hands, recruiting processes specific to motor preparation, while the RH is specialized for mental rotation of external objects.