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Moritz Helias

Publications and source records attributed to Moritz Helias.

At least 55 records · Page 3Linked to original sources

Statistical field theory for neural networks

These notes attempt a self-contained introduction into statistical field theory applied to neural networks of rate units and binary spins. The presentation consists of three parts: First, the introduction of fundamental notions of probabilities, moments, cumulants, and their relation by the linked cluster theorem, of which Wick's theorem is the most important special case; followed by the diagrammatic formulation of perturbation theory, reviewed in the statistical setting. Second, dynamics described by stochastic differential equations in the Ito-formulation, treated in the Martin-Siggia-Rose-De Dominicis-Janssen path integral formalism. With concepts from disordered systems, we then study networks with random connectivity and derive their self-consistent dynamic mean-field theory, explaining the statistics of fluctuations and the emergence of different phases with regular and chaotic dynamics. Third, we introduce the effective action, vertex functions, and the loopwise expansion. These tools are illustrated by systematic derivations of self-consistency equations, going beyond the mean-field approximation. These methods are applied to the pairwise maximum entropy (Ising spin) model, including the recently-found diagrammatic derivation of the Thouless-Anderson-Palmer mean field theory.

cond-mat.dis-nn↗

Expansion of the effective action around non-Gaussian theories

This paper derives the Feynman rules for the diagrammatic perturbation expansion of the effective action around an arbitrary solvable problem. The perturbation expansion around a Gaussian theory is well known and composed of one-line irreducible diagrams only. For the expansions around an arbitrary, non-Gaussian problem, we show that a more general class of irreducible diagrams remains in addition to a second set of diagrams that has no analogue in the Gaussian case. The effective action is central to field theory, in particular to the study of phase transitions, symmetry breaking, effective equations of motion, and renormalization. We exemplify the method on the Ising model, where the effective action amounts to the Gibbs free energy, recovering the Thouless-Anderson-Palmer mean-field theory in a fully diagrammatic derivation. Higher order corrections follow with only minimal effort compared to existing techniques. Our results show further that the Plefka expansion and the high-temperature expansion are special cases of the general formalism presented here.

cond-mat.stat-mech↗

Optimal sequence memory in driven random networks

Autonomous randomly coupled neural networks display a transition to chaos at a critical coupling strength. We here investigate the effect of a time-varying input on the onset of chaos and the resulting consequences for information processing. Dynamic mean-field theory yields the statistics of the activity, the maximum Lyapunov exponent, and the memory capacity of the network. We find an exact condition that determines the transition from stable to chaotic dynamics and the sequential memory capacity in closed form. The input suppresses chaos by a dynamic mechanism, shifting the transition to significantly larger coupling strengths than predicted by local stability analysis. Beyond linear stability, a regime of coexistent locally expansive, but non-chaotic dynamics emerges that optimizes the capacity of the network to store sequential input.

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Locking of correlated neural activity to ongoing oscillations

Population-wide oscillations are ubiquitously observed in mesoscopic signals of cortical activity. In these network states a global oscillatory cycle modulates the propensity of neurons to fire. Synchronous activation of neurons has been hypothesized to be a separate channel of signal processing information in the brain. A salient question is therefore if and how oscillations interact with spike synchrony and in how far these channels can be considered separate. Experiments indeed showed that correlated spiking co-modulates with the static firing rate and is also tightly locked to the phase of beta-oscillations. While the dependence of correlations on the mean rate is well understood in feed-forward networks, it remains unclear why and by which mechanisms correlations tightly lock to an oscillatory cycle. We here demonstrate that such correlated activation of pairs of neurons is qualitatively explained by periodically-driven random networks. We identify the mechanisms by which covariances depend on a driving periodic stimulus. Mean-field theory combined with linear response theory yields closed-form expressions for the cyclostationary mean activities and pairwise zero-time-lag covariances of binary recurrent random networks. Two distinct mechanisms cause time-dependent covariances: the modulation of the susceptibility of single neurons (via the external input and network feedback) and the time-varying variances of single unit activities. For some parameters, the effectively inhibitory recurrent feedback leads to resonant covariances even if mean activities show non-resonant behavior. Our analytical results open the question of time-modulated synchronous activity to a quantitative analysis.

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Perfect spike detection via time reversal

Spiking neuronal networks are usually simulated with three main simulation schemes: the classical time-driven and event-driven schemes, and the more recent hybrid scheme. All three schemes evolve the state of a neuron through a series of checkpoints: equally spaced in the first scheme and determined neuron-wise by spike events in the latter two. The time-driven and the hybrid scheme determine whether the membrane potential of a neuron crosses a threshold at the end of of the time interval between consecutive checkpoints. Threshold crossing can, however, occur within the interval even if this test is negative. Spikes can therefore be missed. The present work derives, implements, and benchmarks a method for perfect retrospective spike detection. This method can be applied to neuron models with affine or linear subthreshold dynamics. The idea behind the method is to propagate the threshold with a time-inverted dynamics, testing whether the threshold crosses the neuron state to be evolved, rather than vice versa. Algebraically this translates into a set of inequalities necessary and sufficient for threshold crossing. This test is slower than the imperfect one, but faster than an alternative perfect tests based on bisection or root-finding methods. Comparison confirms earlier results that the imperfect test rarely misses spikes (less than a fraction $1/10^8$ of missed spikes) in biologically relevant settings. This study offers an alternative geometric point of view on neuronal dynamics.

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How the connectivity structure of neuronal networks influences responses to oscillatory stimuli

Propagation of oscillatory signals through the cortex and coherence is shaped by the connectivity structure of neuronal circuits. This study systematically investigates the network and stimulus properties that shape network responses. The results show how input to a cortical column model of the primary visual cortex excites dynamical modes determined by the laminar pattern. Stimulating the inhibitory neurons in the upper layer reproduces experimentally observed resonances at gamma frequency whose origin can be traced back to two anatomical sub-circuits. We develop this result systematically: Initially, we highlight the effect of stimulus amplitude and filter properties of the neurons on their response to oscillatory stimuli. Subsequently, we analyze the amplification of oscillatory stimuli by the effective network structure. We demonstrate that the amplification of stimuli, as well as their visibility in different populations, can be explained by specific network patterns. Inspired by experimental results we ask whether the anatomical origin of oscillations can be inferred by applying oscillatory stimuli. We find that different network motifs can generate similar responses to oscillatory input, showing that resonances in the network response cannot, straightforwardly, be assigned to the motifs they emerge from. Applying the analysis to a spiking model of a cortical column, we characterize how the dynamic mode structure, which is induced by the laminar connectivity, processes external input. In particular, we show that a stimulus applied to specific populations typically elicits responses of several interacting modes. The resulting network response is therefore composed of a multitude of contributions and can therefore neither be assigned to a single mode nor do the observed resonances necessarily coincide with the intrinsic resonances of the circuit.

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Fundamental activity constraints lead to specific interpretations of the connectome

The continuous integration of experimental data into coherent models of the brain is an increasing challenge of modern neuroscience. Such models provide a bridge between structure and activity, and identify the mechanisms giving rise to experimental observations. Nevertheless, structurally realistic network models of spiking neurons are necessarily underconstrained even if experimental data on brain connectivity are incorporated to the best of our knowledge. Guided by physiological observations, any model must therefore explore the parameter ranges within the uncertainty of the data. Based on simulation results alone, however, the mechanisms underlying stable and physiologically realistic activity often remain obscure. We here employ a mean-field reduction of the dynamics, which allows us to include activity constraints into the process of model construction. We shape the phase space of a multi-scale network model of the vision-related areas of macaque cortex by systematically refining its connectivity. Fundamental constraints on the activity, i.e., prohibiting quiescence and requiring global stability, prove sufficient to obtain realistic layer- and area-specific activity. Only small adaptations of the structure are required, showing that the network operates close to an instability. The procedure identifies components of the network critical to its collective dynamics and creates hypotheses for structural data and future experiments. The method can be applied to networks involving any neuron model with a known gain function.

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Integration of continuous-time dynamics in a spiking neural network simulator

Contemporary modeling approaches to the dynamics of neural networks consider two main classes of models: biologically grounded spiking neurons and functionally inspired rate-based units. The unified simulation framework presented here supports the combination of the two for multi-scale modeling approaches, the quantitative validation of mean-field approaches by spiking network simulations, and an increase in reliability by usage of the same simulation code and the same network model specifications for both model classes. While most efficient spiking simulations rely on the communication of discrete events, rate models require time-continuous interactions between neurons. Exploiting the conceptual similarity to the inclusion of gap junctions in spiking network simulations, we arrive at a reference implementation of instantaneous and delayed interactions between rate-based models in a spiking network simulator. The separation of rate dynamics from the general connection and communication infrastructure ensures flexibility of the framework. We further demonstrate the broad applicability of the framework by considering various examples from the literature ranging from random networks to neural field models. The study provides the prerequisite for interactions between rate-based and spiking models in a joint simulation.

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Functional methods for disordered neural networks

Neural networks of the brain form one of the most complex systems we know. Many qualitative features of the emerging collective phenomena, such as correlated activity, stability, response to inputs, chaotic and regular behavior, can, however, be understood in simple models that are accessible to a treatment in statistical mechanics, or, more precisely, classical statistical field theory. This tutorial presents the fundamentals behind contemporary developments in the theory of neural networks of rate units that are based on methods from statistical mechanics of classical systems with a large number of interacting degrees of freedom. In particular we will focus on a relevant class of systems that have quenched (time independent) disorder. In neural networks, the main source of disorder arises from random synaptic couplings between neurons. These systems are in many respects similar to spin glasses. The tutorial therefore also explains the methods for these disordered systems as far as they are applied in neuroscience. The presentation consists of two parts. In the first part we introduce stochastic differential equations in the Martin - Siggia - Rose - De Dominicis - Janssen path integral formalism. In the second part we employ this language to derive the dynamic mean-field theory for deterministic random networks, the basis of the seminal work by Sompolinsky, Crisanti, Sommers 1988, as well as a recent extension to stochastic dynamics.

cond-mat.dis-nn↗

Identifying anatomical origins of coexisting oscillations in the cortical microcircuit

Oscillations are omnipresent in neural population signals, like multi-unit recordings, EEG/MEG, and the local field potential. They have been linked to the population firing rate of neurons, with individual neurons firing in a close-to-irregular fashion at low rates. Using a combination of mean-field and linear response theory we predict the spectra generated in a layered microcircuit model of V1, composed of leaky integrate-and-fire neurons and based on connectivity compiled from anatomical and electrophysiological studies. The model exhibits low- and high-gamma oscillations visible in all populations. Since locally generated frequencies are imposed onto other populations, the origin of the oscillations cannot be deduced from the spectra. We develop an universally applicable systematic approach that identifies the anatomical circuits underlying the generation of oscillations in a given network. Based on a theoretical reduction of the dynamics, we derive a sensitivity measure resulting in a frequency-dependent connectivity map that reveals connections crucial for the peak amplitude and frequency of the observed oscillations and identifies the minimal circuit generating a given frequency. The low-gamma peak turns out to be generated in a sub-circuit located in layer 2/3 and 4, while the high-gamma peak emerges from the inter-neurons in layer 4. Connections within and onto layer 5 are found to regulate slow rate fluctuations. We further demonstrate how small perturbations of the crucial connections have significant impact on the population spectra, while the impairment of other connections leaves the dynamics on the population level unaltered. The study uncovers connections where mechanisms controlling the spectra of the cortical microcircuit are most effective.

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Pairwise maximum-entropy models and their Glauber dynamics: bimodality, bistability, non-ergodicity problems, and their elimination via inhibition

Pairwise maximum-entropy models have been used in recent neuroscientific literature to predict the activity of neuronal populations, given only the time-averaged correlations of the neuron activities. This paper provides evidence that the pairwise model, applied to experimental recordings, predicts a bimodal distribution for the population-averaged activity, and for some population sizes the second mode peaks at high activities, with 90% of the neuron population active within time-windows of few milliseconds. This bimodality has several undesirable consequences: 1. The presence of two modes is unrealistic in view of observed neuronal activity. 2. The prediction of a high-activity mode is unrealistic on neurobiological grounds. 3. Boltzmann learning becomes non-ergodic, hence the pairwise model found by this method is not the maximum entropy distribution; similarly, solving the inverse problem by common variants of mean-field approximations has the same problem. 4. The Glauber dynamics associated with the model is either unrealistically bistable, or does not reflect the distribution of the pairwise model. This bimodality is first demonstrated for an experimental dataset comprising 159 neuron activities recorded from the motor cortex of macaque monkey. Using a reduced maximum-entropy model, evidence is then provided that this bimodality affects typical neural recordings of population sizes of a couple of hundreds or more neurons. As a way to eliminate the bimodality and its ensuing problems, a modified pairwise model is presented, which -- most important -- has an associated pairwise Glauber dynamics. This model avoids bimodality thanks to a minimal asymmetric inhibition. It can be interpreted as a minimum-relative-entropy model with a particular prior, or as a maximum-entropy model with an additional constraint.

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Distributions of covariances as a window into the operational regime of neuronal networks

Massively parallel recordings of spiking activity in cortical networks show that covariances vary widely across pairs of neurons. Their low average is well understood, but an explanation for the wide distribution in relation to the static (quenched) disorder of the connectivity in recurrent random networks was so far elusive. We here derive a finite-size mean-field theory that reduces a disordered to a highly symmetric network with fluctuating auxiliary fields. The exposed analytical relation between the statistics of connections and the statistics of pairwise covariances shows that both, average and dispersion of the latter, diverge at a critical coupling. At this point, a network of nonlinear units transits from regular to chaotic dynamics. Applying these results to recordings from the mammalian brain suggests its operation close to this edge of criticality.

cond-mat.dis-nn↗

A reaction diffusion-like formalism for plastic neural networks reveals dissipative solitons at criticality

Self-organized structures in networks with spike-timing dependent plasticity (STDP) are likely to play a central role for information processing in the brain. In the present study we derive a reaction-diffusion-like formalism for plastic feed-forward networks of nonlinear rate neurons with a correlation sensitive learning rule inspired by and being qualitatively similar to STDP. After obtaining equations that describe the change of the spatial shape of the signal from layer to layer, we derive a criterion for the non-linearity necessary to obtain stable dynamics for arbitrary input. We classify the possible scenarios of signal evolution and find that close to the transition to the unstable regime meta-stable solutions appear. The form of these dissipative solitons is determined analytically and the evolution and interaction of several such coexistent objects is investigated.

cond-mat.dis-nn↗

Correlated fluctuations in strongly-coupled binary networks beyond equilibrium

Randomly coupled Ising spins constitute the classical model of collective phenomena in disordered systems, with applications covering ferromagnetism, combinatorial optimization, protein folding, stock market dynamics, and social dynamics. The phase diagram of these systems is obtained in the thermodynamic limit by averaging over the quenched randomness of the couplings. However, many applications require the statistics of activity for a single realization of the possibly asymmetric couplings in finite-sized networks. Examples include reconstruction of couplings from the observed dynamics, learning in the central nervous system by correlation-sensitive synaptic plasticity, and representation of probability distributions for sampling-based inference. The systematic cumulant expansion for kinetic binary (Ising) threshold units with strong, random and asymmetric couplings presented here goes beyond mean-field theory and is applicable outside thermodynamic equilibrium; a system of approximate non-linear equations predicts average activities and pairwise covariances in quantitative agreement with full simulations down to hundreds of units. The linearized theory yields an expansion of the correlation- and response functions in collective eigenmodes, leads to an efficient algorithm solving the inverse problem, and shows that correlations are invariant under scaling of the interaction strengths.

cond-mat.dis-nn↗

Modulated escape from a metastable state driven by colored noise

Many phenomena in nature are described by excitable systems driven by colored noise. The temporal correlations in the fluctuations hinder an analytical treatment. We here present a general method of reduction to a white-noise system, capturing the color of the noise by effective and time-dependent boundary conditions. We apply the formalism to a model of the excitability of neuronal membranes, the leaky integrate-and-fire neuron model, revealing an analytical expression for the linear response of the system valid up to moderate frequencies. The closed form analytical expression enables the characterization of the response properties of such excitable units and the assessment of oscillations emerging in networks thereof.

cond-mat.stat-mech↗

Reduction of colored noise in excitable systems to white noise and dynamic boundary conditions

A recent study on the effect of colored driving noise on the escape from a metastable state derives an analytic expression of the transfer function of the leaky integrate-and-fire neuron model subject to colored noise. Here we present an alternative derivation of the results, taking into account time-dependent boundary conditions explicitly. This systematic approach may facilitate future extensions beyond first order perturbation theory. The analogy of the quantum harmonic oscillator to the LIF neuron model subject to white noise enables a derivation of the well known transfer function simpler than the original approach. We offer a pedagogical presentation including all intermediate steps of the calculations.

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Scalability of asynchronous networks is limited by one-to-one mapping between effective connectivity and correlations

Network models are routinely downscaled compared to nature in terms of numbers of nodes or edges because of a lack of computational resources, often without explicit mention of the limitations this entails. While reliable methods have long existed to adjust parameters such that the first-order statistics of network dynamics are conserved, here we show that limitations already arise if also second-order statistics are to be maintained. The temporal structure of pairwise averaged correlations in the activity of recurrent networks is determined by the effective population-level connectivity. We first show that in general the converse is also true and explicitly mention degenerate cases when this one-to-one relationship does not hold. The one-to-one correspondence between effective connectivity and the temporal structure of pairwise averaged correlations implies that network scalings should preserve the effective connectivity if pairwise averaged correlations are to be held constant. Changes in effective connectivity can even push a network from a linearly stable to an unstable, oscillatory regime and vice versa. On this basis, we derive conditions for the preservation of both mean population-averaged activities and pairwise averaged correlations under a change in numbers of neurons or synapses in the asynchronous regime typical of cortical networks. We find that mean activities and correlation structure can be maintained by an appropriate scaling of the synaptic weights, but only over a range of numbers of synapses that is limited by the variance of external inputs to the network. Our results therefore show that the reducibility of asynchronous networks is fundamentally limited.

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The correlation structure of local cortical networks intrinsically results from recurrent dynamics

The co-occurrence of action potentials of pairs of neurons within short time intervals is known since long. Such synchronous events can appear time-locked to the behavior of an animal and also theoretical considerations argue for a functional role of synchrony. Early theoretical work tried to explain correlated activity by neurons transmitting common fluctuations due to shared inputs. This, however, overestimates correlations. Recently the recurrent connectivity of cortical networks was shown responsible for the observed low baseline correlations. Two different explanations were given: One argues that excitatory and inhibitory population activities closely follow the external inputs to the network, so that their effects on a pair of cells mutually cancel. Another explanation relies on negative recurrent feedback to suppress fluctuations in the population activity, equivalent to small correlations. In a biological neuronal network one expects both, external inputs and recurrence, to affect correlated activity. The present work extends the theoretical framework of correlations to include both contributions and explains their qualitative differences. Moreover the study shows that the arguments of fast tracking and recurrent feedback are not equivalent, only the latter correctly predicts the cell-type specific correlations.

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