Time-course of cortical networks involved in working memory.

Working memory (WM) is one of the most studied cognitive constructs. Although many neuroimaging studies have identified brain networks involved in WM, the time course of these networks remains unclear. In this paper we use dense-array electroencephalography (dEEG) to capture neural signals during performance of a standard WM task, the n-back task, and a blend of principal components analysis and independent components analysis (PCA/ICA) to statistically identify networks of WM and their time courses. Results reveal a visual cortex centric network, that also includes the posterior cingulate cortex, that is active prior to stimulus onset and that appears to reflect anticipatory, attention-related processes. After stimulus onset, the ventromedial prefrontal cortex, lateral prefrontal prefrontal cortex, and temporal poles become associated with the prestimulus network. This second network appears to reflect executive control processes. Following activation of the second network, the cortices of the temporo-parietal junction with the temporal lobe structures seen in the first and second networks re-engage. This third network appears to reflect activity of the ventral attention network involved in control of attentional reorientation. The results point to important temporal features of network dynamics that integrate multiple subsystems of the ventral attention network with the default mode network in the performance of working memory tasks.

When and where perceptual load interacts with voluntary visuospatial attention: an event-related potential and dipole modeling study.

Perceptual load is recognized to affect visual selective attention, but at an unknown spatiotemporal locus in the brain. To examine this issue, event-related potentials (ERPs) were recorded while participants performed an orientation discrimination task, under conditions of low or high perceptual load. Participants were required to respond to targets (10% of trials) presented in the attended visual field while ignoring all stimuli in the unattended visual field. The interaction between voluntary attention and perceptual load was significant for the posterior N1 component (190 ms) but not for the earlier C1 (84 ms) or P1 (100 ms) components. This load by attention interaction for N1 was localized to the temporoparietal-occipital (TPO) gyrus by dipole modeling analysis. Dipole modeling also showed that a reversed attentional effect in the C1 time range was due to ERP overlap from the subsequent attention-sensitive P1 component. Results suggest that perceptual load affects voluntary visuospatial attention at an early (but not the earliest) processing stage and that the TPO gyrus mediates target selection at the discrimination stage.

Aging and repetition priming for targets and distracters in a working memory task.

A combined working memory/repetition priming task was administered to 13 young (mean age 23) and 13 elderly (mean age 69) adults. Each participant memorized a sample target face at the beginning of a trial and then determined whether each of 13 serially presented test faces matched the sample target. In each trial, both the target and one particular distracter face were repeated during the test phase. Within-trial repetition priming effects indicated the contribution of implicit memory to task performance. Response times decreased as items were tested repeatedly within a trial, but this decrement was greater for distracters than for targets. Young and older participants were equally accurate at identifying targets, but elderly were slightly less accurate for distracters. Elderly participants showed repetition priming effects for both targets and distracters, while the young showed such effects only for distracters. The results suggest that active maintenance in working memory, but not inhibition or rejection of distracters, may suppress implicit memory systems.

Event-related potentials reveal dissociable mechanisms for orienting and focusing visuospatial attention.

The neural mechanisms supporting visuospatial orienting and focusing were investigated by recording event-related potentials (ERPs) in a cued, line-orientation discrimination task. Search arrays flashed randomly in the left or right visual field and were preceded by peripheral cues that varied in validity (valid or invalid, with 50% each) and size (large or small, with 50% each). Facilitation of response time was observed for valid trials, regardless of cue size. In contrast to previous cued search studies, however, small (i.e., more precise) cues were associated with delayed responses. Both the timing and the amplitudes of the early ERP components, P1 and N1, were modulated by attentional orienting, with valid trials eliciting a larger and later contralateral vP1 (ventral P1) and a smaller and later contralateral N1 compared to invalid trials. Attentional focusing modulated only the amplitudes of the P1 component, with precisely cued trials eliciting a larger dP1 (dorsal P1) than less precisely cued trials at both contralateral and ipsilateral sites. Thus, both attentional orienting and focusing modulate early stimulus processing stages that overlap in time, but with dissociable effects on the scalp distribution of these components, indicating possibly different underlying mechanisms. In addition, the results support the notion that voluntary and involuntary allocations of visuospatial attention are mediated by different underlying neural processes.

Incentive-elicited brain activation in adolescents: similarities and differences from young adults.

Brain motivational circuitry in human adolescence is poorly characterized. One theory holds that risky behavior in adolescence results in part from a relatively overactive ventral striatal (VS) motivational circuit that readily energizes approach toward salient appetitive cues. However, other evidence fosters a theory that this circuit is developmentally underactive, in which adolescents approach more robust incentives (such as risk taking or drug experimentation) to recruit this circuitry. To help resolve this, we compared brain activation in 12 adolescents (12-17 years of age) and 12 young adults (22-28 years of age) while they anticipated the opportunity to respond to obtain monetary gains as well as to avoid monetary losses. In both age groups, anticipation of potential gain activated portions of the VS, right insula, dorsal thalamus, and dorsal midbrain, where the magnitude of VS activation was sensitive to gain amount. Notification of gain outcomes (in contrast with missed gains) activated the mesial frontal cortex (mFC). Across all subjects, signal increase in the right nucleus accumbens during anticipation of responding for large gains independently correlated with both age and self-rated excitement about the high gain cue. In direct comparison, adolescents evidenced less recruitment of the right VS and right-extended amygdala while anticipating responding for gains (in contrast with anticipation of nongains) compared with young adults. However, brain activation after gain outcomes did not appreciably differ between age groups. These results suggest that adolescents selectively show reduced recruitment of motivational but not consummatory components of reward-directed behavior.

The role of memory representation in the vigilance decrement.

Working memory load is critically important for the overall level of performance on vigilance tasks. However, its role in a key aspect of vigilance-sensitivity decrement over time-is unclear. We used a dual-task procedure in which either a spatial or a nonspatial working memory task was performed simultaneously with a spatial vigilance task for 20 min. Sensitivity in the vigilance task declined over time when the concurrent task involved spatial working memory. In contrast, there was no sensitivity decrement with a nonspatial working memory task. The results provide the first evidence of a specific role for working memory representation in vigilance decrement. The findings are also consistent with a multiple resource theory in which separate resources for memory representation and cognitive control operations are differentially susceptible to depletion over time, depending on the demands of the task at hand.