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Jens Christian Claussen

Publications and source records attributed to Jens Christian Claussen.

At least 19 recordsLinked to original sources

A Mathematical Framework for Misinformation Propagation in Complex Networks: Topology-Dependent Distortion and Control

Misinformation is pervasive in natural, biological, social, and engineered systems, yet its quantitative characterization remains challenging. We develop a general mathematical framework for quantifying information distortion in distributed systems by modeling how local transmission errors accumulate along network geodesics and reshape each agent's perceived global state. Through a drift-fluctuation decomposition of pathwise binomial noise, we derive closed-form expressions for node-level perception distributions and show that directional bias induces only a uniform shift in the mean, preserving the fluctuation structure. Applying the framework to canonical graph ensembles, we uncover strong topological signatures of misinformation: Erdős-Rényi random graphs exhibit a double-peaked distortion profile driven by connectivity transitions and geodesic-length fluctuations, scale-free networks suppress misinformation through hub-mediated integration, and optimally rewired small-world networks achieve comparable suppression by balancing clustering with short paths. A direct comparison across regular lattices, Erdős-Rényi random graphs, Watts-Strogatz small-world networks, and Barabási-Albert scale-free networks reveals a connectivity-dependent crossover. In the extremely sparse regime, scale-free and Erdős-Rényi networks behave similarly. At intermediate sparsity, Watts-Strogatz small-world networks exhibit the lowest misinformation. In contrast, Barabás-Albert scale-free networks maintain low misinformation in sparse and dense regimes, while regular lattices produce the highest distortion across connectivities. We additionally show how sparsity constraints, structural organization, and connection costs delineate regimes of minimal misinformation.

physics.soc-ph↗

Partial synchronization in empirical brain networks as a model for unihemispheric sleep

We analyze partial synchronization patterns in a network of FitzHugh-Nagumo oscillators with empirical structural connectivity measured in healthy human subjects. We report a dynamical asymmetry between the hemispheres, induced by the natural structural asymmetry. We show that the dynamical asymmetry can be enhanced by introducing the inter-hemispheric coupling strength as a control parameter for partial synchronization patterns. We specify the possible modalities for existence of unihemispheric sleep in human brain, where one hemisphere sleeps while the other remains awake. In fact, this state is common among migratory birds and mammals like aquatic species.

nlin.AO↗

Chimera patterns under the impact of noise

We investigate two types of chimera states, i.e., patterns consisting of coexisting spatially separated domains with coherent and incoherent dynamics, in ring networks of Stuart-Landau oscillators with symmetry-breaking coupling, under the influence of noise. Amplitude chimeras are characterized by temporally periodic dynamics throughout the whole network, but spatially incoherent behavior with respect to the amplitudes in a part of the system; they are long-living transients. Chimera death states generalize chimeras to stationary inhomogeneous patterns (oscillation death), which combine spatially coherent and incoherent domains. We analyze the impact of random perturbations, addressing the question of robustness of chimera states in the presence of white noise. We further consider the effect of symmetries applied to random initial conditions.

nlin.AO↗

Evolutionary Dynamics for Persistent Cooperation in Structured Populations

The emergence and maintenance of cooperative behavior is a fascinating topic in evolutionary biology and social science. The public goods game (PGG) is a paradigm for exploring cooperative behavior. In PGG, the total resulting payoff is divided equally among all participants. This feature still leads to the dominance of defection without substantially magnifying the public good by a multiplying factor. Much effort has been made to explain the evolution of cooperative strategies, including a recent model in which only a portion of the total benefit is shared by all the players through introducing a new strategy named persistent cooperation. A persistent cooperator is a contributor who is willing to pay a second cost to retrieve the remaining portion of the payoff contributed by themselves. In a previous study, this model was analyzed in the framework of well-mixed populations. This paper focuses on discussing the persistent cooperation in lattice-structured populations. The evolutionary dynamics of the structured populations consisting of three types of competing players (pure cooperators, defectors and persistent cooperators) are revealed by theoretical analysis and numerical simulations. In particular, the approximate expressions of fixation probabilities for strategies are derived on one-dimensional lattices. The phase diagrams of stationary states, the evolution of frequencies and spatial patterns for strategies are illustrated on both one-dimensional and square lattices by simulations. Our results are consistent with the general observation that, at least in most situations, a structured population facilitates the evolution of cooperation. Specifically, here we find that the existence of persistent cooperators greatly suppresses the spreading of defectors under more relaxed conditions in structured populations compared to that obtained in well-mixed population.

q-bio.PE↗

A model for dynamical evolution of science in space

How does the topological space of science emerge? Inspired by the concept of maps of science, i.e. mapping scientific topics to a scientific space, we ask which topological structure a dynamical process of authors collaborating and publishing papers can generate. We propose a dynamical process where papers as well as new groups receive topical positions embedded in a two-dimensional euclidean space. The precise position of new papers depends on previous topics of the respective authors and is chosen randomly in a surrounding neighborhood including novelty and interdisciplinarity. Depending on parameters, the spatial structure resembles a simple Gaussian distribution, or spatial clusters of side-topics are observed. We quantify the time-evolution of the spatial structure and discuss the influence of inhomogenities.

physics.soc-ph↗

Induction of slow oscillations by rhythmic acoustic stimulation

Slow oscillations are electrical potential oscillations with a spectral peak frequency of $\sim$0.8 Hz, and hallmark the electroencephalogram during slow-wave sleep. Recent studies have indicated a causal contribution of slow oscillations to the consolidation of memories during slow-wave sleep, raising the question to what extent such oscillations can be induced by external stimulation. Here, we examined whether slow oscillations can be effectively induced by rhythmic acoustic stimulation. Human subjects were examined in three conditions: (i) with tones presented at a rate of 0.8 Hz (`0.8-Hz stimulation'); (ii) with tones presented at a random sequence (`random stimulation'); and (iii) with no tones presented in a control condition (`sham'). Stimulation started during wakefulness before sleep and continued for the first $\sim$90 min of sleep. Compared with the other two conditions, 0.8-Hz stimulation significantly delayed sleep onset. However, once sleep was established, 0.8-Hz stimulation significantly increased and entrained endogenous slow oscillation activity. Sleep after the 90-min period of stimulation did not differ between the conditions. Our data show that rhythmic acoustic stimulation can be used to effectively enhance slow oscillation activity. However, the effect depends on the brain state, requiring the presence of stable non-rapid eye movement sleep.

q-bio.NC↗

Modeling effect of GABAergic current in a basal ganglia computational model

Electrical high frequency stimulation (HFS) of deep brain regions is a method shown to be clinically effective in different types of movement and neurological disorders. In order to shed light on its mode of action a computational model of the basal ganglia network coupled the HFS as injection current into the cells of the subthalamic nucleus (STN). Its overall increased activity rendered a faithful transmission of sensorimotor input through thalamo-cortical relay cells possible. Our contribution uses this model by Rubin and Terman (J Comput Neurosci, 16, 211-223, 2004) as a starting point and integrates recent findings on the importance of the extracellular concentrations of the inhibiting neurotransmitter GABA. We are able to show in this computational study that besides electrical stimulation a high concentration of GABA and its resulting conductivity in STN cells is able to re-establish faithful thalamocortical relaying, which otherwise broke down in the simulated parkinsonian state.

q-bio.NC↗

Sleep, Neuroengineering and Dynamics

Modeling of consciousness-related phenomena and neuroengineering are fields that are rapidly growing together. We review recent approaches and developments and point out some promising directions of future research: Understanding the dynamics of consciousness states and associated oscillations, pathological oscillations as well as their treatment by stimulation, neuroprosthetics and brain-computer-interface approaches, and stimulation approaches that probe, influence and strengthen memory consolidation. In all these fields, computational models connect theory, neurophysiology and neuroengineering research and pave a way towards medical applications.

q-bio.NC↗

The phase response of the cortical slow oscillation

Cortical slow oscillations occur in the mammalian brain during deep sleep and have been shown to contribute to memory consolidation, an effect that can be enhanced by electrical stimulation. As the precise underlying working mechanisms are not known it is desired to develop and analyze computational models of slow oscillations and to study the response to electrical stimuli. In this paper we employ the conductance based model of Compte et al. [J Neurophysiol 89, 2707] to study the effect of electrical stimulation. The population response to electrical stimulation depends on the timing of the stimulus with respect to the state of the slow oscillation. First, we reproduce the experimental results of electrical stimulation in ferret brain slices by Shu et al. [Nature 423, 288] from the conductance based model. We then numerically obtain the phase response curve for the conductance based network model to quantify the network's response to weak stimuli. Our results agree with experiments in vivo and in vitro that show that sensitivity to stimulation is weaker in the up than in the down state. However, we also find that within the up state stimulation leads to a shortening of the up state, or phase advance, whereas during the up-down transition a prolongation of up states is possible, resulting in a phase delay. Finally, we compute the phase response curve for the simple mean-field model by Ngo et al. [Europhys Lett 89, 68002] and find that the qualitative shape of the PRC is preserved, despite its different mechanism for the generation of slow oscillations.

q-bio.NC↗

Desynchronizing effect of high-frequency stimulation in a generic cortical network model

Transcranial Electrical Stimulation (TCES) and Deep Brain Stimulation (DBS) are two different applications of electrical current to the brain used in different areas of medicine. Both have a similar frequency dependence of their efficiency, with the most pronounced effects around 100Hz. We apply superthreshold electrical stimulation, specifically depolarizing DC current, interrupted at different frequencies, to a simple model of a population of cortical neurons which uses phenomenological descriptions of neurons by Izhikevich and synaptic connections on a similar level of sophistication. With this model, we are able to reproduce the optimal desynchronization around 100Hz, as well as to predict the full frequency dependence of the efficiency of desynchronization, and thereby to give a possible explanation for the action mechanism of TCES.

q-bio.NC↗

Stochastic differential equations for evolutionary dynamics with demographic noise and mutations

We present a general framework to describe the evolutionary dynamics of an arbitrary number of types in finite populations based on stochastic differential equations (SDE). For large, but finite populations this allows to include demographic noise without requiring explicit simulations. Instead, the population size only rescales the amplitude of the noise. Moreover, this framework admits the inclusion of mutations between different types, provided that mutation rates, $μ$, are not too small compared to the inverse population size 1/N. This ensures that all types are almost always represented in the population and that the occasional extinction of one type does not result in an extended absence of that type. For $μN\ll1$ this limits the use of SDE's, but in this case there are well established alternative approximations based on time scale separation. We illustrate our approach by a Rock-Scissors-Paper game with mutations, where we demonstrate excellent agreement with simulation based results for sufficiently large populations. In the absence of mutations the excellent agreement extends to small population sizes.

q-bio.PE↗

Stabilization of biodiversity in the coevolutionary rock-paper-scissors game on complex networks

The dynamical mechanisms that can stabilize the coexistence of species (or strategies) are of substantial interest for the maintenance of biodiversity and in sociobehavioural dynamics. We investigate the mean extinction time in the coevolutionary dynamics of three cyclically invading strategies for different evolutionary processes on various classes of complex networks, including random graphs, scale-free and small world networks. We find that scale-free and random graphs lead to a strong stabilization of coexistence both for the Moran process and the Local Update process. The stabilization is of an order of magnitude stronger compared to a lattice topology, and is mainly caused by the degree heterogeneity of the graph. However, evolutionary processes on graphs can be defined in many variants, and we show that in a process using effective payoffs the effect of the network topology can be completely reversed. Thus, stabilization of coexistence depends on both network geometry and underlying evolutionary process.

q-bio.PE↗

Mean extinction times in cyclic coevolutionary rock-paper-scissors dynamics

Dynamical mechanisms that can stabilize the coexistence or diversity in biology are generally of fundamental interest. In contrast to many two-strategy evolutionary games, games with three strategies and cyclic dominance like the rock-paper-scissors game (RPS) stabilize coexistence and thus preserve biodiversity in this system. In the limit of infinite populations, resembling the traditional picture of evolutionary game theory, replicator equations predict the existence of a fixed point in the interior of the phase space. But in finite populations, strategy frequencies will run out of the fixed point because of stochastic fluctuations, and strategies can even go extinct. For three different processes and for zero-sum and non-zero-sum RPS as well, we present results of extensive simulations for the mean extinction time (MET), depending on the number of agents N, and we introduce two analytical approaches for the derivation of the MET.

q-bio.PE↗

Triggering up states in all-to-all coupled neurons

Slow-wave sleep in mammalians is characterized by a change of large-scale cortical activity currently paraphrased as cortical Up/Down states. A recent experiment demonstrated a bistable collective behaviour in ferret slices, with the remarkable property that the Up states can be switched on and off with pulses, or excitations, of same polarity; whereby the effect of the second pulse significantly depends on the time interval between the pulses. Here we present a simple time discrete model of a neural network that exhibits this type of behaviour, as well as quantitatively reproduces the time-dependence found in the experiments.

q-bio.NC↗

Floquet Stability Analysis of Ott-Grebogi-Yorke and Difference Control

Stabilization of instable periodic orbits of nonlinear dynamical systems has been a widely explored field theoretically and in applications. The techniques can be grouped in time-continuous control schemes based on Pyragas, and the two Poincaré-based chaos control schemes, Ott-Gebogi-Yorke (OGY) and difference control. Here a new stability analysis of these two Poincaré-based chaos control schemes is given by means of Floquet theory. This approach allows to calculate exactly the stability restrictions occuring for small measurement delays and for an impulse length shorter than the length of the orbit. This is of practical experimental relevance; to avoid a selection of the relative impulse length by trial and error, it is advised to investigate whether the used control scheme itself shows systematic limitations on the choice of the impulse length. To investigate this point, a Floquet analysis is performed. For OGY control the influence of the impulse length is marginal. As an unexpected result, difference control fails when the impulse length is taken longer than a maximal value that is approximately one half of the orbit length for small Ljapunov numbers and decreases with the Ljapunov number.

nlin.CD↗

Discrete stochastic processes, replicator and Fokker-Planck equations of coevolutionary dynamics in finite and infinite populations

Finite-size fluctuations in coevolutionary dynamics arise in models of biological as well as of social and economic systems. This brief tutorial review surveys a systematic approach starting from a stochastic process discrete both in time and state. The limit $N\to \infty$ of an infinite population can be considered explicitly, generally leading to a replicator-type equation in zero order, and to a Fokker-Planck-type equation in first order in $1/\sqrt{N}$. Consequences and relations to some previous approaches are outlined.

q-bio.PE↗

Cyclic dominance and biodiversity in well-mixed populations

Coevolutionary dynamics is investigated in chemical catalysis, biological evolution, social and economic systems. The dynamics of these systems can be analyzed within the unifying framework of evolutionary game theory. In this Letter, we show that even in well-mixed finite populations, where the dynamics is inherently stochastic, biodiversity is possible with three cyclic dominant strategies. We show how the interplay of evolutionary dynamics, discreteness of the population, and the nature of the interactions influences the coexistence of strategies. We calculate a critical population size above which coexistence is likely.

q-bio.PE↗

Offdiagonal complexity: A computationally quick network complexity measure. Application to protein networks and cell division

Many complex biological, social, and economical networks show topologies drastically differing from random graphs. But, what is a complex network, i.e.\ how can one quantify the complexity of a graph? Here the Offdiagonal Complexity (OdC), a new, and computationally cheap, measure of complexity is defined, based on the node-node link cross-distribution, whose nondiagonal elements characterize the graph structure beyond link distribution, cluster coefficient and average path length. The OdC apporach is applied to the {\sl Helicobacter pylori} protein interaction network and randomly rewired surrogates thereof. In addition, OdC is used to characterize the spatial complexity of cell aggregates. We investigate the earliest embryo development states of Caenorhabditis elegans. The development states of the premorphogenetic phase are represented by symmetric binary-valued cell connection matrices with dimension growing from 4 to 385. These matrices can be interpreted as adjacency matrix of an undirected graph, or network. The OdC approach allows to describe quantitatively the complexity of the cell aggregate geometry.

q-bio.QM↗