3,586 research outputs found

    A spiral attractor network drives rhythmic locomotion

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    The joint activity of neural populations is high dimensional and complex. One strategy for reaching a tractable understanding of circuit function is to seek the simplest dynamical system that can account for the population activity. By imaging Aplysia’s pedal ganglion during fictive locomotion, here we show that its population wide activity arises from a low-dimensional spiral attractor. Evoking locomotion moved the population into a low-dimensional, periodic, decaying orbit - a spiral – in which it behaved as a true attractor, converging to the same orbit when evoked, and returning to that orbit after transient perturbation. We found the same attractor in every preparation, and could predict motor output directly from its orbit, yet individual neurons’ participation changed across consecutive locomotion bouts. From these results, we propose that only the low-dimensional dynamics for movement control, and not the high-dimensional population activity, are consistent within and between nervous systems

    Nonlinear brain dynamics as macroscopic manifestation of underlying many-body field dynamics

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    Neural activity patterns related to behavior occur at many scales in time and space from the atomic and molecular to the whole brain. Here we explore the feasibility of interpreting neurophysiological data in the context of many-body physics by using tools that physicists have devised to analyze comparable hierarchies in other fields of science. We focus on a mesoscopic level that offers a multi-step pathway between the microscopic functions of neurons and the macroscopic functions of brain systems revealed by hemodynamic imaging. We use electroencephalographic (EEG) records collected from high-density electrode arrays fixed on the epidural surfaces of primary sensory and limbic areas in rabbits and cats trained to discriminate conditioned stimuli (CS) in the various modalities. High temporal resolution of EEG signals with the Hilbert transform gives evidence for diverse intermittent spatial patterns of amplitude (AM) and phase modulations (PM) of carrier waves that repeatedly re-synchronize in the beta and gamma ranges at near zero time lags over long distances. The dominant mechanism for neural interactions by axodendritic synaptic transmission should impose distance-dependent delays on the EEG oscillations owing to finite propagation velocities. It does not. EEGs instead show evidence for anomalous dispersion: the existence in neural populations of a low velocity range of information and energy transfers, and a high velocity range of the spread of phase transitions. This distinction labels the phenomenon but does not explain it. In this report we explore the analysis of these phenomena using concepts of energy dissipation, the maintenance by cortex of multiple ground states corresponding to AM patterns, and the exclusive selection by spontaneous breakdown of symmetry (SBS) of single states in sequences.Comment: 31 page

    Dysfunctions of highly parallel real-time machines as 'developmental disorders': Security concerns and a Caveat Emptor

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    A cognitive paradigm for gene expression in developmental biology that is based on rigorous application of the asymptotic limit theorems of information theory can be adapted to highly parallel real-time computing. The coming Brave New World of massively parallel 'autonomic' and 'Self-X' machines driven by the explosion of multiple core and molecular computing technologies will not be spared patterns of canonical and idiosyncratic failure analogous to the developmental disorders affecting organisms that have had the relentless benefit of a billion years of evolutionary pruning. This paper provides a warning both to potential users of these machines and, given that many such disorders can be induced by external agents, to those concerned with larger scale matters of homeland security

    Network analysis of the cellular circuits of memory

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    Intuitively, memory is conceived as a collection of static images that we accumulate as we experience the world. But actually, memories are constantly changing through our life, shaped by our ongoing experiences. Assimilating new knowledge without corrupting pre-existing memories is then a critical brain function. However, learning and memory interact: prior knowledge can proactively influence learning, and new information can retroactively modify memories of past events. The hippocampus is a brain region essential for learning and memory, but the network-level operations that underlie the continuous integration of new experiences into memory, segregating them as discrete traces while enabling their interaction, are unknown. Here I show a network mechanism by which two distinct memories interact. Hippocampal CA1 neuron ensembles were monitored in mice as they explored a familiar environment before and after forming a new place-reward memory in a different environment. By employing a network science representation of the co-firing relationships among principal cells, I first found that new associative learning modifies the topology of the cells’ co-firing patterns representing the unrelated familiar environment. I fur- ther observed that these neuronal co-firing graphs evolved along three functional axes: the first segregated novelty; the second distinguished individual novel be- havioural experiences; while the third revealed cross-memory interaction. Finally, I found that during this process, high activity principal cells rapidly formed the core representation of each memory; whereas low activity principal cells gradually joined co-activation motifs throughout individual experiences, enabling cross-memory in- teractions. These findings reveal an organizational principle of brain networks where high and low activity cells are differentially recruited into coactivity motifs as build- ing blocks for the flexible integration and interaction of memories. Finally, I employ a set of manifold learning and related approaches to explore and characterise the complex neural population dynamics within CA1 that underlie sim- ple exploration.Open Acces

    Solvable Neural Network Model for Input-Output Associations: Optimal Recall at the Onset of Chaos

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    In neural information processing, an input modulates neural dynamics to generate a desired output. To unravel the dynamics and underlying neural connectivity enabling such input-output association, we proposed an exactly soluble neural-network model with a connectivity matrix explicitly consisting of inputs and required outputs. An analytic form of the response upon the input is derived, whereas three distinctive types of responses including chaotic dynamics as bifurcation against input strength are obtained depending on the neural sensitivity and number of inputs. Optimal performance is achieved at the onset of chaos, and the relevance of the results to cognitive dynamics is discussed

    A robot model of the basal ganglia: Behavior and intrinsic processing

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    The existence of multiple parallel loops connecting sensorimotor systems to the basal ganglia has given rise to proposals that these nuclei serve as a selection mechanism resolving competitions between the alternative actions available in a given context. A strong test of this hypothesis is to require a computational model of the basal ganglia to generate integrated selection sequences in an autonomous agent, we therefore describe a robot architecture into which such a model is embedded, and require it to control action selection in a robotic task inspired by animal observations. Our results demonstrate effective action selection by the embedded model under a wide range of sensory and motivational conditions. When confronted with multiple, high salience alternatives, the robot also exhibits forms of behavioral disintegration that show similarities to animal behavior in conflict situations. The model is shown to cast light on recent neurobiological findings concerning behavioral switching and sequencing

    Learning and Production of Movement Sequences: Behavioral, Neurophysiological, and Modeling Perspectives

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    A growing wave of behavioral studies, using a wide variety of paradigms that were introduced or greatly refined in recent years, has generated a new wealth of parametric observations about serial order behavior. What was a mere trickle of neurophysiological studies has grown to a more steady stream of probes of neural sites and mechanisms underlying sequential behavior. Moreover, simulation models of serial behavior generation have begun to open a channel to link cellular dynamics with cognitive and behavioral dynamics. Here we summarize the major results from prominent sequence learning and performance tasks, namely immediate serial recall, typing, 2XN, discrete sequence production, and serial reaction time. These populate a continuum from higher to lower degrees of internal control of sequential organization. The main movement classes covered are speech and keypressing, both involving small amplitude movements that are very amenable to parametric study. A brief synopsis of classes of serial order models, vis-Ă -vis the detailing of major effects found in the behavioral data, leads to a focus on competitive queuing (CQ) models. Recently, the many behavioral predictive successes of CQ models have been joined by successful prediction of distinctively patterend electrophysiological recordings in prefrontal cortex, wherein parallel activation dynamics of multiple neural ensembles strikingly matches the parallel dynamics predicted by CQ theory. An extended CQ simulation model-the N-STREAMS neural network model-is then examined to highlight issues in ongoing attemptes to accomodate a broader range of behavioral and neurophysiological data within a CQ-consistent theory. Important contemporary issues such as the nature of working memory representations for sequential behavior, and the development and role of chunks in hierarchial control are prominent throughout.Defense Advanced Research Projects Agency/Office of Naval Research (N00014-95-1-0409); National Institute of Mental Health (R01 DC02852
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