Trends in Cognitive Sciences
Capacity limits of information processing in the brain
Section snippets
Capacity limit in explicit visual event detection: the attentional blink
Virtually all models of visual cognition distinguish between capacity–unlimited and capacity-limited stages of information processing (e.g. 3, 4). In these two-stage models, an early stage permits the rapid, initial evaluation of the visual world, whereas later attention-demanding, capacity-limited stages are necessary for the conscious report of the stimuli. The dual nature of visual cognition is well illustrated by the attentional blink (AB) paradigm: when subjects attempt to identify two
The neural basis of the AB bottleneck
Two-stage models of the AB have received considerable support from event-related potential (ERP) studies. T2 target words that are not explicitly perceived in an AB paradigm nonetheless elicit an N400, an electrophysiological marker of semantic processing [15], whereas successful detection of T2 elicits a P300 [9], an electrophysiological marker of working memory updating. Thus, T2 targets that fail to reach working memory are nevertheless processed up to the semantic level.
Functional magnetic
Capacity limits of visual short term memory (VSTM)
Our visual cognition is not only limited by the rate at which information can be attended or consolidated into VSTM, it is also limited by the amount of information that can be stored in VSTM. Although the capacity of VSTM is generally estimated to be about 4 items 28, 29, 30, it is set not only by the number of objects but also by the complexity of each object [31]. This capacity limit has significant behavioral consequences. For instance, VSTM storage capacity is thought to be at least partly
The neural basis of VSTM storage capacity limits
Visual working memory is mediated by a network of brain regions distributed across the cerebral cortex 41, 42, 43. This network can be loosely divided into regions that contribute to Baddeley's [34] central executive system, and regions involved in maintaining the information in working memory (i.e. VSTM). Executive processes, such as encoding, manipulation and retrieval of information from working memory, have been primarily associated with the frontal/prefrontal cortex 44, 45. By contrast,
The limits of response selection: the psychological refractory period
A third major bottleneck of information processing takes place when an appropriate action has to be selected in response to a stimulus. This is evidenced by the psychological refractory period (PRP) paradigm [55]: when subjects are required to perform two sensorimotor tasks in rapid succession, the response to the second task is increasingly delayed as the stimulus onset asynchrony (SOA) between the two tasks decrease (Figure 3a). This occurs even when sensory and motor modalities are distinct
Neural correlates of the psychological refractory period
Electrophysiological studies of the PRP have established the temporal boundary of the PRP bottleneck to a stage between stimulus consolidation in working memory and motor preparation 66, 67, and split-brain patient studies implicate a sub-cortical component to the PRP 68, 69. By contrast, imaging studies have primarily aimed at localizing the cortical substrates of the PRP. Although the neural basis of dual-task interference has received considerable attention over the past 10 years [70], only
Convergence of processing limitations?
This review has so far discussed capacity limits in encoding visual information in working memory (AB), in maintaining and monitoring that information (VSTM and MOT), and in selecting an appropriate response for it (PRP), as if these tapped into strictly independent stages of information processing. Indeed, perceptual and response limitations have traditionally been viewed as such [55]. However, this view has been challenged by findings that the AB and PRP partly share a common capacity-limited
The functional neuroanatomy of processing bottlenecks: a synthesis
Another approach to assessing the relationship between processing bottlenecks is to determine whether they engage similar neural substrates. Although demonstrating that two cognitive processes activate similar brain regions does not necessarily imply that these processes overlap at the cellular level, the failure to find such common foci of activation would rule out the possibility that these processes affect each other through a common neural substrate. Figure 4 shows the brain regions
Conclusion
This review of the literature supports the view that the neural substrates of VSTM storage capacity are primarily localized to posterior cortical regions, and predicts that distinct regions of visual cortex may contribute to separate forms of VSTM storage capacity. By contrast, the AB and PRP bottlenecks are most likely to result from the interaction between foci of a distributed fronto-parietal – and probably visual – cortical network, with individual nodes of the network (e.g. lateral frontal
Acknowledgements
This work was supported by grants from NSF and NIMH to R.M. and from CICN and NSERC (Canada) to J.I.
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