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Showing posts with the label reinforcement learning

Metastability and Eye Movements: A Dynamical‑Systems Interpretation

  1. Why metastability is a natural language for gaze behavior The idea that perception, attention, and neural activity evolve through transiently stable states has deep roots in cognitive science and neuroscience. Concepts such as attractors , basins , noise‑induced transitions , and escape times appear in work on perceptual switching, decision‑making, and neural population dynamics (Kelso, 1995; Rabinovich et al., 2008; Deco & Jirsa, 2012). Eye movements, especially the alternation between fixations and saccades ,   fit remarkably well into this metastable picture. The Freidlin–Wentzell theory of rare events (Freidlin & Wentzell, 2012) provides a rigorous mathematical language for these intuitions. 2. Fixations as metastable states  Consider the gaze position X t as the state of a stochastic dynamical system. During a fixation the  gaze remains confined to a small region, microsaccades and noise generate small fluctuations, and the gaze tends to return...

A Two-Layered Diffusion Model Traces the Dynamics of Information Processing in the Valuation-and-Choice Circuit of Decision Making

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A circuit of evaluation and selection of the alternatives ( see here ) is considered a reliable model in neurobiology. In this published study , valuation and choice of a decisional process during Two-Alternative Forced-Choice ( TAFC ) task are represented as a two-layered network of computational cells, where information accrual and processing progress in nonlinear diffusion dynamics.  The evolution of the response-to-stimulus map is thus modeled by two linked diffusive modules ( 2LDM ) representing the neuronal populations involved in the valuation-and-decision circuit of decision making (Figure 1). Diffusion models are naturally appropriate for describing accumulation of evidence over the time [ see here ] . This allows the computation of the response times (RTs) in valuation and choice, under the hypothesis of ex-Wald distribution. A nonlinear transfer function integrates the activities of the two layers. The input-output map based on the infomax principle makes the 2LD...

THE BASAL GANGLIA CIRCUIT

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The basal ganglia (BG) are a set of subcortical nuclei (Figure 1). They receive cortical and thalamic input mainly through the striatum (i.e., by the putamen and the caudate nucleus) which forms the input layer of BG. Next, the information flows through the globus pallidus to the major output layer, the substantia nigra pars reticulata (SNr). There also exists an internal loop between the globus pallidus and the subthalamic nucleus. The substantia nigra pars compacta (SNc) projects back to the striatum with dopaminergic neurons . The input layer of BG is rich of spiny neurons (SP), which receive huge cortical (C) connections. The SPs also receive afferents from dopaminergic neurons (DA) in SNc which synapse on to the SPs in the striatum. Inhibitory dynamics are also present in the BG. The activity of the SPs inhibits the DA neurons in the SNc. The subthalamic side-loop, on the contrary, disinhibits the DA which can result in the excitation of the DA neurons proportional to the input...

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