Our ability to selectively focus attention on elements of our sensory environment is a critical cognitive function that enables us to enhance the processing of high priority stimuli. Both electrophysiological and hemodynamic brain imaging studies have implicated a network of brain areas in the frontal and parietal cortices as playing a role in imparting top-down attentional control to influence processing in low-level sensory cortices. In the previous grant period we used functional MRI (fMRI) and event-related potentials (ERPs) to help delineate the neural cascade of activations in specific regions in this control network during the voluntary orienting of attention, as well as various of the ways in which voluntary attention can modulate processing in the sensory cortices. However, many facets of the mechanisms by which attention facilitates our performance in the real world remain unclear. For example, most of our previous work focused on the mechanisms of voluntary attention when it was either directed in a sustained way to a particular location or stimulus channel, or when it needed to be oriented only relatively slowly. It seems likely, however, that for rapid spatial shifts of attention the neural control mechanisms differ in some important ways. Moreover, there are numerous other fundamental and ecologically important ways in which attention is invoked for enhancing the processing of relevant stimuli. For example, attentional shifts and attentional control can also be initiated by viewing an individual's eye gaze, by visual-popout stimuli, and by stimulus conflict, all of which appear to induce the engagement of attention in a faster and more automatized way than with endogenous instructional cues. However, the temporal cascade of the neural processes underlying attentional control and influence in these other circumstances has yet to be delineated. In the next period of this grant, we propose to continue our programmatic investigation of the neural mechanisms of attention with a new set of studies directed toward these other fundamental ways in which attentional control and influence is invoked. These will include study of: (1) the rapid shifting of both voluntary and gaze-cue-triggered visual spatial attention, (2) the shifting and focusing of spatial attention within a complex visual scene;and (3) the invocation of attention for detecting and resolving conflicting visual stimulus information. As before, we plan to combine ERPs, EEG, fMRI, and behavioral measures to perform these studies, with the aim to delineate the timing, sequence, and location of the neural processes and network dynamics involved in these cognitive functions, thereby gaining insight into the underlying mechanisms.

Public Health Relevance

Attention is a critical cognitive function that allows us to dynamically select for detailed analysis the most pertinent information in our environment from moment to moment. This project is aimed at elucidating the basic neural mechanisms of visual attention, and thus is relevant for what normal individuals do constantly throughout their lives. In addition, attentional deficits form key components of a variety of mental and neural illnesses, including schizophrenia, Attention Deficit and Hyperactivity Disorder (ADHD), autism, and disorders of visual perception, and thus elucidating the basic cognitive brain mechanisms of attention is essential to both mental and neural health research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH060415-08
Application #
8020118
Study Section
Special Emphasis Panel (ZRG1-IFCN-A (03))
Program Officer
Rossi, Andrew
Project Start
2001-04-05
Project End
2014-01-31
Budget Start
2011-02-01
Budget End
2012-01-31
Support Year
8
Fiscal Year
2011
Total Cost
$383,328
Indirect Cost
Name
Duke University
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Fornaciai, Michele; Brannon, Elizabeth M; Woldorff, Marty G et al. (2017) Numerosity processing in early visual cortex. Neuroimage 157:429-438
Green, Jessica J; Boehler, Carsten N; Roberts, Kenneth C et al. (2017) Cortical and Subcortical Coordination of Visual Spatial Attention Revealed by Simultaneous EEG-fMRI Recording. J Neurosci 37:7803-7810
San Martín, René; Appelbaum, Lawrence G; Huettel, Scott A et al. (2016) Cortical Brain Activity Reflecting Attentional Biasing Toward Reward-Predicting Cues Covaries with Economic Decision-Making Performance. Cereb Cortex 26:1-11
Langford, Zachary D; Krebs, Ruth M; Talsma, Durk et al. (2016) Strategic down-regulation of attentional resources as a mechanism of proactive response inhibition. Eur J Neurosci 44:2095-103
Marini, Francesco; Demeter, Elise; Roberts, Kenneth C et al. (2016) Orchestrating Proactive and Reactive Mechanisms for Filtering Distracting Information: Brain-Behavior Relationships Revealed by a Mixed-Design fMRI Study. J Neurosci 36:988-1000
van den Berg, Berry; Appelbaum, Lawrence G; Clark, Kait et al. (2016) Visual search performance is predicted by both prestimulus and poststimulus electrical brain activity. Sci Rep 6:37718
Park, Joonkoo; DeWind, Nicholas K; Woldorff, Marty G et al. (2016) Rapid and Direct Encoding of Numerosity in the Visual Stream. Cereb Cortex 26:748-763
Donohue, Sarah E; Appelbaum, Lawrence G; McKay, Cameron C et al. (2016) The neural dynamics of stimulus and response conflict processing as a function of response complexity and task demands. Neuropsychologia 84:14-28
Clark, Kait; Appelbaum, L Gregory; van den Berg, Berry et al. (2015) Improvement in visual search with practice: mapping learning-related changes in neurocognitive stages of processing. J Neurosci 35:5351-9
Marini, Francesco; van den Berg, Berry; Woldorff, Marty G (2015) Reward-prospect interacts with trial-by-trial preparation for potential distraction. Vis cogn 23:313-335

Showing the most recent 10 out of 68 publications