62 research outputs found

    Slow Convergence in Generalized Central Limit Theorems

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    We study the central limit theorem in the non-normal domain of attraction to symmetric α\alpha-stable laws for 0<α20<\alpha\leq2. We show that for i.i.d. random variables XiX_i, the convergence rate in LL^\infty of both the densities and distributions of inXi/(n1/αL(n))\sum_i^n X_i/(n^{1/\alpha}L(n)) is at best logarithmic if LL is a non-trivial slowly varying function. Asymptotic laws for several physical processes have been derived using central limit theorems with nlogn\sqrt{n\log n} scaling and Gaussian limiting distributions. Our result implies that such asymptotic laws are accurate only for exponentially large nn.Comment: To appear in Comptes Rendus de l'Acad\'emie des Sciences, Math\'ematique

    Infinitesimal phase response functions can be misleading

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    Phase response functions are the central tool in the mathematical analysis of pulse-coupled oscillators. When an oscillator receives a brief input pulse, the phase response function specifies how its phase is altered, as a function of the phase at which the input arrives. When the pulse is weak, it is customary to linearize the dependence of the response on pulse strength. The result is called the {\em infinitesimal} phase response function. These ideas have been used extensively in theoretical biology and also in some areas of engineering. I give an example in which the infinitesimal phase response function predicts that two oscillators, as they exchange pulses back and fourth, will converge to synchrony. Using the true phase response, I prove this prediction to be false for all positive interaction strengths. For short, the analogue of the Hartman-Grobman theorem that one might, at first sight, expect to hold is invalid

    Approximate, not perfect synchrony maximizes the downstream effectiveness of excitatory neuronal ensembles

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    The most basic functional role commonly ascribed to synchrony in the brain is that of amplifying excitatory neuronal signals. The reasoning is straightforward: When positive charge is injected into a leaky target neuron over a time window of positive duration, some of it will have time to leak back out before an action potential is triggered in the target, and it will in that sense be wasted. If the goal is to elicit a firing response in the target using as little charge as possible, it seems best to deliver the charge all at once, i.e., in perfect synchrony. In this article, we show that this reasoning is correct only if one assumes that the input ceases when the target crosses the firing threshold, but before it actually fires. If the input ceases later-for instance, in response to a feedback signal triggered by the firing of the target-the "most economical" way of delivering input (the way that requires the least total amount of input) is no longer precisely synchronous, but merely approximately so. If the target is a heterogeneous network, as it always is in the brain, then ceasing the input "when the target crosses the firing threshold" is not an option, because there is no single moment when the firing threshold is crossed. In this sense, precise synchrony is never optimal in the brain.R01 NS067199 - NINDS NIH HH

    Domain imbedding methods for the Stokes equations

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    We study direct and iterative domain imbedding methods for the Stokes equations on certain non-rectangular domains in two space dimensions. We analyze a continuous analog of numerical domain imbedding for bounded, smooth domains, and give an example of a simple numerical algorithm suggested by the continuous analysis. This algorithms is applicable for simply connected domains which can be covered by rectangular grids, with uniformly spaced grid lines in at least one coordinate direction. We also discuss a related FFT-based fast solver for Stokes problems with physical boundary conditions on rectangles, and present some numerical results.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46324/1/211_2005_Article_BF01386422.pd

    A blue sky bifurcation in the dynamics of political candidates

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    Political candidates often shift their positions opportunistically in hopes of capturing more votes. When there are only two candidates, the best strategy for each of them is often to move towards the other. This eventually results in two centrists with coalescing views. However, the strategy of moving towards the other candidate ceases to be optimal when enough voters abstain instead of voting for a centrist who does not represent their views. These observations, formalized in various ways, have been made many times. Our own formalization is based on differential equations. The surprise and main result derived from these equations is that the final candidate positions can jump discontinuously as the voters' loyalty towards their candidate wanes. The underlying mathematical mechanism is a blue sky bifurcation

    Neurosystems: brain rhythms and cognitive processing

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    Neuronal rhythms are ubiquitous features of brain dynamics, and are highly correlated with cognitive processing. However, the relationship between the physiological mechanisms producing these rhythms and the functions associated with the rhythms remains mysterious. This article investigates the contributions of rhythms to basic cognitive computations (such as filtering signals by coherence and/or frequency) and to major cognitive functions (such as attention and multi-modal coordination). We offer support to the premise that the physiology underlying brain rhythms plays an essential role in how these rhythms facilitate some cognitive operations.098352 - Wellcome Trust; 5R01NS067199 - NINDS NIH HH

    ODEs and Mandatory Voting

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    This paper presents mathematics relevant to the question whether voting should be mandatory. Assuming a static distribution of voters' political beliefs, we model how politicians might adjust their positions to raise their share of the vote. Various scenarios can be explored using our web-based app (see text for the link). Abstentions are found to have great impact on the dynamics of candidates, and in particular to introduce the possibility of discontinuous jumps in optimal candidate positions. This is a paper intended for undergraduate students. It is an unusual application of ODEs. We hope that it might help engage some students who may find it harder to connect with the more customary applications from the natural sciences.Comment: 16 page

    Minimal Size of Cell Assemblies Coordinated by Gamma Oscillations

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    In networks of excitatory and inhibitory neurons with mutual synaptic coupling, specific drive to sub-ensembles of cells often leads to gamma-frequency (25–100 Hz) oscillations. When the number of driven cells is too small, however, the synaptic interactions may not be strong or homogeneous enough to support the mechanism underlying the rhythm. Using a combination of computational simulation and mathematical analysis, we study the breakdown of gamma rhythms as the driven ensembles become too small, or the synaptic interactions become too weak and heterogeneous. Heterogeneities in drives or synaptic strengths play an important role in the breakdown of the rhythms; nonetheless, we find that the analysis of homogeneous networks yields insight into the breakdown of rhythms in heterogeneous networks. In particular, if parameter values are such that in a homogeneous network, it takes several gamma cycles to converge to synchrony, then in a similar, but realistically heterogeneous network, synchrony breaks down altogether. This leads to the surprising conclusion that in a network with realistic heterogeneity, gamma rhythms based on the interaction of excitatory and inhibitory cell populations must arise either rapidly, or not at all. For given synaptic strengths and heterogeneities, there is a (soft) lower bound on the possible number of cells in an ensemble oscillating at gamma frequency, based simply on the requirement that synaptic interactions between the two cell populations be strong enough. This observation suggests explanations for recent experimental results concerning the modulation of gamma oscillations in macaque primary visual cortex by varying spatial stimulus size or attention level, and for our own experimental results, reported here, concerning the optogenetic modulation of gamma oscillations in kainate-activated hippocampal slices. We make specific predictions about the behavior of pyramidal cells and fast-spiking interneurons in these experiments.Collaborative Research in Computational NeuroscienceNational Institutes of Health (U.S.) (grant 1R01 NS067199)National Institutes of Health (U.S.) (grant DMS 0717670)National Institutes of Health (U.S.) (grant 1R01 DA029639)National Institutes of Health (U.S.) (grant 1RC1 MH088182)National Institutes of Health (U.S.) (grant DP2OD002002)Paul G. Allen Family FoundationnGoogle (Firm

    The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse

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    A population of uncoupled neurons can often be brought close to synchrony by a single strong inhibitory input pulse affecting all neurons equally. This mechanism is thought to underlie some brain rhythms, in particular gamma frequency (30–80 Hz) oscillations in the hippocampus and neocortex. Here we show that synchronization by an inhibitory input pulse often fails for populations of classical Hodgkin–Huxley neurons. Our reasoning suggests that in general, synchronization by inhibitory input pulses can fail when the transition of the target neurons from rest to spiking involves a Hopf bifurcation, especially when inhibition is shunting, not hyperpolarizing. Surprisingly, synchronization is more likely to fail when the inhibitory pulse is stronger or longer-lasting. These findings have potential implications for the question which neurons participate in brain rhythms, in particular in gamma oscillations
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