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2008, Lecture Notes in Computer Science
…
17 pages
1 file
Research on spatial attention traditionally focuses on how it is influenced by the location of objects within the visual environment. However, a primary function of spatial attention is to plan physical actions. When events occur in the world, visual information needs to be integrated with current body position to help prepare effective responses to these events. Further, current actions can subsequently influence further deployments of attention. Thus, spatial attention must be considered within the context of the body. Here we present research demonstrating that one's own body and the actions of others can influence spatial attention mechanisms, influencing the prioritization of functional space near the body and the direction of attention. This work emphasizes a need for an embodied theory of spatial attention and a more dynamic neural model of attention that adjusts to meet the demands of the current environment and the perceiver's goals.
Attention, Perception, & Psychophysics, 2010
Research confirms that the body influences perception, but little is known about the embodiment of attention. We investigated whether the implied actions of others direct spatial attention, using a lateralized covert-orienting task with nonpredictive central cues depicting static, right/left-facing bodies poised in midaction. Validity effects (decreased response times for validly compared with invalidly cued trials) indicated orienting in the direction of the implied action. In Experiment 1, we compared action (running, throwing) with nonaction (standing) cues. Only the action cues produced validity effects, suggesting that implied action directs attention. The action cues produced faster responses overall, suggesting that action cues prime motor responses. In Experiment 2, we determined whether action cues shifted attention in a specific direction rather than to a general side of space: Two cues had similar action speed and motor effort but differed in implied direction (jumping, vertical; throwing, horizontal). Validity effects were found only for the throw cues for which the implied motion direction was consistent with lateralized target locations. In Experiment 3, we compared block-like stimuli to the throwing action stimuli to examine whether lower level perceptual information could account for the attention effects alone. Validity effects were found only for the human-action stimuli. Overall, the results suggest that predictive simulations of action shift attention in action-consistent directions.
Experimental Brain Research, 2007
Humans use the same representations to code self-produced and observed actions. Neurophysiological evidence for this view comes from the discovery of the so-called mirror neurons in premotor cortex of the macaque monkey. These neurons respond when the monkey performs a particular action but also when it observes the same behavior in another individual. In humans, such direct links between perception and action seem to mediate action priming, where a response is facilitated when a similar action is observed. An issue that has not been fully resolved concerns the role of selective attention in these processes. Action priming appears to be an automatic process in the sense that the observed action can be irrelevant to the observer's task and nevertheless prime similar responses. However, it is not known whether attention has to be oriented to the action for these processes to be engaged. It is demonstrated here that spatial attention indeed has to be oriented to the action related body site for action priming to take place. Furthermore, if attention is oriented to the appropriate body site, there need be no visual cues to action for action priming to emerge.
Frontiers in Psychology, 2013
Previous research has shown that attention is prioritized for the space near the hand, leading to faster detection of visual targets appearing close to one's own hand. In the present study, we examined whether observers are also facilitated in detecting targets presented near another's hand by having participants perform a Posner cueing task while sitting next to a friend. Across blocks, either the participant or the friend placed a hand next to one of the target locations. Our results robustly showed that participants detected targets appearing near their own hands more quickly than targets appearing away from their hands, replicating previous work demonstrating that spatial attention is prioritized near one's own hand (Experiments 1-4). No such attentional bias effects were found for targets appearing near the friend's hand, suggesting that spatial attention is not automatically prioritized near another's hand (Experiments 1 and 2). However, participants were faster to detect targets near the friend's hand following a joint action task, suggesting a shared body representation plays an influential role in biasing attention to the space near another's hand (Experiment 4).
Journal of Experimental Psychology: Human Perception and Performance, 2006
This study explored whether hand location affected spatial attention. The authors used a visual covertorienting paradigm to examine whether spatial attention mechanisms-location prioritization and shifting attention-were supported by bimodal, hand-centered representations of space. Placing 1 hand next to a target location, participants detected visual targets following highly predictive visual cues. There was no a priori reason for the hand to influence task performance unless hand presence influenced attention. Results showed that target detection near the hand was facilitated relative to detection away from the hand, regardless of cue validity. Similar facilitation was found with only proprioceptive or visual hand location information but not with arbitrary visual anchors or distant targets. Hand presence affected attentional prioritization of space, not the shifting of attention.
Social Cognition, 2010
The present study examined whether and how the presence of an invisible person can affect the control of visuospatial attention on the basis of cues.
Frontiers in Integrative Neuroscience, 6, art.nr. 4, 2012
The role of body orientation in the orienting and allocation of social attention was examined using an adapted Simon paradigm. Participants categorized the facial expression of forward facing, computer-generated human figures by pressing one of two response keys, each located left or right of the observers' body midline, while the orientation of the stimulus figure's body (trunk, arms, and legs), which was the task-irrelevant feature of interest, was manipulated (oriented toward the left or right visual hemifield) with respect to the spatial location of the required response. We found that when the orientation of the body was compatible with the required response location, responses were slower relative to when body orientation was incompatible with the response location. In line with a model put forward by Hietanen (1999), this reverse compatibility effect suggests that body orientation is automatically processed into a directional spatial code, but that this code is based on an integration of head and body orientation within an allocentric-based frame of reference. Moreover, we argue that this code may be derived from the motion information implied in the image of a figure when head and body orientation are incongruent. Our results have implications for understanding the nature of the information that affects the allocation of attention for social orienting.
2016
Social stimuli are a highly salient source of information, and seem to possess unique qualities that set them apart from other well-known categories. One characteristic is their ability to elicit spatial orienting, whereby directional stimuli like eyegaze and pointing gestures act as exogenous cues that trigger automatic shifts of attention that are difficult to inhibit. This effect has been extended to non-social stimuli, like arrows, leading to some uncertainty regarding whether spatial orienting is specialized for social cues. Using a standard spatial cueing paradigm, we found evidence that both a pointing hand and arrow are effective cues, but that the hand is encoded more quickly, leading to overall faster responses. We then extended the paradigm to include multiple cues in order to evaluate congruent vs. incongruent cues. Our results indicate that faster encoding of the social cue leads to downstream effects on the allocation of attention resulting in faster orienting.
Cognition, 2004
Functional neuroimaging research has shown that certain classes of visual stimulus selectively activate focal regions of visual cortex. Specifically, cortical areas that generally and selectively respond to faces (
British Journal of Psychology, 2010
We discuss evidence indicating that human visual attention is strongly modulated by the potential of objects for action. The possibility of action between multiple objects enables the objects to be attended as a single group, and the fit between individual objects in a group and the action that can be performed influences responses to group members. In addition, having a goal state to perform a particular action affects the stimuli that are selected along with the features and area of space that is attended. These effects of action may reflect statistical learning between environmental cues that are linked by action and/or the coupling between perception and action systems in the brain. The data support the argument that visual selection is a flexible process that emerges as a need to prioritize objects for action.
Experimental Brain Research, 2011
Analogously to the visual system, somatosensory processing may be segregated into two streams, with the body constituting either part of the action system or a perceptual object. Experimental studies with participants free from neurological disease which test this hypothesis are rare, however. The present study explored the contributions of the two putative streams to a task that requires participants to estimate the spatial properties of their own body. Two manipulations from the visuospatial literature were included. First, participants were required to point either backward towards pre-defined landmarks on their own body (egocentric reference frame) or to a forward projection of their own body (allocentric representation). Second, a manipulation of movement mode was included, requiring participants to perform pointing movements either immediately, or after a fixed delay, following instruction. Results show that accessing an allocentric representation of one's own body results in performance changes. Specifically, the spatial bias shown to exist for body space when pointing backward at one's own body disappears when participants are requested to mentally project their body to a pre-defined location in front space. Conversely, delayed execution of pointing movements does not result in performance changes. Altogether, these findings provide support for a constrained dual stream hypothesis of somatosensory processing and are the first to show similarities in the processing of body space and peripersonal space.
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