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Our ability to overcome habitual responses in favor of goal-driven novel responses depends on frontoparietal cognitive control networks (CCNs). Recent and ongoing work is revealing the brain network and information processes that allow CCNs to generate cognitive flexibility. First, working memory processes necessary for flexible maintenance and manipulation of goal-relevant representations were recently found to depend on short-term network plasticity (in contrast to persistent activity) within CCN regions. Second, compositional (i.e. abstract and reusable) rule representations maintained within CCNs have been found to reroute network activity flows from stimulus to response, enabling flexible behavior. Together, these findings suggest cognitive flexibility is enhanced by CCN-coordinated network mechanisms, utilizing compositional reuse of neural representations and network flows to flexibly accomplish task goals. 

A central goal of neuroscience is to understand how function-relevant brain activations are generated. Here we test the hypothesis that function-relevant brain activations are generated primarily by distributed network flows. We focused on visual processing in human cortex, given the long-standing literature supporting the functional relevance of brain activations in visual cortex regions exhibiting visual category selectivity. We began by using fMRI data from N = 352 human participants to identify category-specific responses in visual cortex for images of faces, places, body parts, and tools. We then systematically tested the hypothesis that distributed network flows can generate these localized visual category selective responses. This was accomplished using a recently developed approach for simulating – in a highly empirically constrained manner – the generation of task-evoked brain activations by modeling activity flowing over intrinsic brain connections. We next tested refinements to our hypothesis, focusing on how stimulus-driven network interactions initialized in V1 generate downstream visual category selectivity. We found evidence that network flows directly from V1 were sufficient for generating visual category selectivity, but that additional, globally distributed (whole-cortex) network flows increased category selectivity further. Using null network architectures we also found that each region’s unique intrinsic “connectivity fingerprint” was key to the generation of category selectivity. These results generalized across regions associated with all four visual categories tested (bodies, faces, places, and tools), and provide evidence that the human brain’s intrinsic network organization plays a prominent role in the generation of functionally relevant, localized responses. 

Abstract Arousal state is regulated by subcortical neuromodulatory nuclei, such as locus coeruleus, which send wide-reaching projections to cortex. Whether higher-order cortical regions have the capacity to recruit neuromodulatory systems to aid cognition is unclear. Here, we hypothesized that select cortical regions activate the arousal system, which, in turn, modulates large-scale brain activity, creating a functional circuit predicting cognitive ability. We utilized the Human Connectome Project 7T functional magnetic resonance imaging dataset (n = 149), acquired at rest with simultaneous eye tracking, along with extensive cognitive assessment for each subject. First, we discovered select frontoparietal cortical regions that drive large-scale spontaneous brain activity specifically via engaging the arousal system. Second, we show that the functionality of the arousal circuit driven by bilateral posterior cingulate cortex (associated with the default mode network) predicts subjects’ cognitive abilities. This suggests that a cortical region that is typically associated with self-referential processing supports cognition by regulating the arousal system. 

Transcranial electrical stimulation (tES) technology and neuroimaging are increasingly coupled in basic and applied science. This synergy has enabled individualized tES therapy and facilitated causal inferences in functional neuroimaging. However, traditional tES paradigms have been stymied by relatively small changes in neural activity and high inter-subject variability in cognitive effects. In this perspective, we propose a tES framework to treat these issues which is grounded in dynamical systems and control theory. The proposed paradigm involves a tight coupling of tES and neuroimaging in which M/EEG is used to parameterize generative brain models as well as control tES delivery in a hybrid closed-loop fashion. We also present a novel quantitative framework for cognitive enhancement driven by a new computational objective: shaping how the brain reacts to potential “inputs” (e.g., task contexts) rather than enforcing a fixed pattern of brain activity. 

System identification poses a significant bottleneck to characterizing and controlling complex systems. This challenge is greatest when both the system states and parameters are not directly accessible, leading to a dual-estimation problem. Current approaches to such problems are limited in their ability to scale with many-parameter systems, as often occurs in networks. In the current work, we present a new, computationally efficient approach to treat large dual-estimation problems. In this work, we derive analytic back-propagated gradients for the Prediction Error Method which enables efficient and accurate identification of large systems. The PEM approach consists of directly integrating state estimation into a dual-optimization objective, leaving a differentiable cost/error function only in terms of the unknown system parameters, which we solve using numerical gradient/Hessian methods. Intuitively, this approach consists of solving for the parameters that generate the most accurate state estimator (Extended/Cubature Kalman Filter). We demonstrate that this approach is at least as accurate in state and parameter estimation as joint Kalman Filters (Extended/Unscented/Cubature) and Expectation-Maximization, despite lower complexity. We demonstrate the utility of our approach by inverting anatomically-detailed individualized brain models from human magnetoencephalography (MEG) data.