optimal channel efficiency in a sensory network · mosqueiro, akimushkin and maia – dincon 2011,...

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Optimal Channel Efficiency in a Sensory Network Thiago S. Mosqueiro and Leonardo P. Maia Institute of Physics of São Carlos, University of São Paulo – 13560-970 São Carlos, SP, Brazil [email protected] Preprint: arXiv:1204.0751v1 We show that the entropy of the distribution of avalanche lifetimes in the Kinouchi-Copelli model always achieves a maximum jointly with the dynamic range. The newly found optimization occurs for all topologies we tested, even when the distribution of avalanche lifetimes itself is not a power-law and when the entropy of the size distribution of avalanches is not concomitantly maximized, strongly suggesting that dynamical rules al- lowing a proper temporal matching of the states of the interacting neurons is the key for achieving good performance in information processing. 1. Introduction In 2003, Beggs and Plenz observed avalanches in cortical tissues Several other groups have reported by now avalanches: Ribeiro et al, PLoS ONE, Public Library of Science, 2010, v. 5, p. e14129 Mazzoni et al, PLoS ONE, Public Library of Science, 2007, v. 2, p. e439 Shew et al, Journal of Neuroscience, 2009, v. 29, p. 15595 Shew et al, Journal of Neuroscience, 2011, v. 31, p. 55 Kinouchi-Copelli model: optimal dynamic range at criticality. We have found: optimization of dynamic range and entropy of lifetimes Channel efficiency (= entropy of lifetimes): efficiency coding info. through firing rate Channel efficiency always exhibit a critical optimization 2. Kinouchi-Copelli Model N nodes connected through adjacency matrix A State of j -th node: X j (t) X j =0: quiescent X j =1: excited m>X j > 1: refractory n 1 n 2 n 3 n 4 n 5 A 12 A 14 A 24 A 43 A 45 A 31 A 53 A 52 Kinouchi and Copelli, Nat. Phys., 2006 Dynamics as follows: if 1 X j (t) m - 2, then X j (t + 1) = X j (t)+1; if X j (t)= m - 1, then X j (t + 1) = 0; if X j (t)=0, then X j (t + 1) = 1 with probability η (external stimulus); A jk , k, by each of its neighbors. Instantaneous mean activity: ρ(t)= N X j =1 X j (t) Mean activity: F T = 1 T T X t=1 ρ(t) Average branching ratio: σ = N X j =1 1 N N X p=1 A jp Dynamic range is an equilibrium measure. 3. Avalanches Activity initiated by a single neuron: burst Avalanches: critical bursts We study distribution of size and duration of these bursts when varying σ Size: number of neurons without repetition Time: number of a single burst time steps Avalanche size and lifetime are out of equilibrium measures. Simulations run 10 6 bursts with N = 10 5 , m = 10 and K ∈{2, 5, 10, 15}. 4. Random graphs – Erd ˝ os-Rényi topology Simulations and theory Size exponent: -3/2 Lifetime exponent: -1.9 Shew et al, Journal of Neuroscience, 2009, 29, 15595-15600 Beggs and Plenz, The Journal of Neuro- science, 2003, 23, 11167-11177 Mosqueiro, Akimushkin and Maia DINCON 2011, doi: 10.5540/DINCON.2011.001.1.0064 5. Scale-free graphs – Barabási-Álbert topology Critical point: σ c =0.4 Lower exponents in power law degree distro.: also exhibit lack of scale invariance Branching process analysis agree with this critical σ Networks with several values of N were tested and no meaningful change was detected in distributions 6. Entropy in both topologies Similar as in Shew et al, Journal of Neuro- science, 2011, 31, 15595 Erd ˝ os-Rényi results Entropy of both avalanche lifetimes and sizes are optimized at criticality Barabási-Álbert results Entropy of avalanche lifetimes is optimized at criticality Dynamic range and avalanche lifetimes are both not optimized at K =2 7. Conclusion Summarizing, we studied the avalanches in Kinouchi-Copelli model in a first attempt to figure out detailed mechanisms of information transmission in sensory systems. We discovered that, in a critical point, the entropy of avalanche lifetime statistics (information efficiency) is always max- imized jointly with the dynamic range, an important measure of information transmission extracted from the tuning curves from psychophysics. Our findings fit in the discussions regarding the role of criticality in information processing and the relationship of long bursts of activity with the dynamic range, specially because they suggest critical behavior without pure scaleinvariance. 8. Acknowledgements The authors would like to thank financial support from CAPES and FAPESP. Poster powered by Fedora 14 Linux, L A T E X, sciposter++, Emacs, GnuPlot and GIMP. Criticality in Neural Systems Symposium, April 30 – May 1, 2012

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Page 1: Optimal Channel Efficiency in a Sensory Network · Mosqueiro, Akimushkin and Maia – DINCON 2011, doi: 10.5540/DINCON.2011.001.1.0064 5. Scale-free graphs – Barabási-Álbert

Optimal Channel Efficiency in aSensory Network

Thiago S. Mosqueiro and Leonardo P. MaiaInstitute of Physics of São Carlos, University of São Paulo – 13560-970 São Carlos, SP, Brazil

[email protected]

Preprint: arXiv:1204.0751v1

We show that the entropy of the distribution of avalanche lifetimes in the Kinouchi-Copellimodel always achieves a maximum jointly with the dynamic range. The newly foundoptimization occurs for all topologies we tested, even when the distribution of avalanchelifetimes itself is not a power-law and when the entropy of the size distribution ofavalanches is not concomitantly maximized, strongly suggesting that dynamical rules al-lowing a proper temporal matching of the states of the interacting neurons is the key forachieving good performance in information processing.

1. Introduction

In 2003, Beggs and Plenz observed avalanches in cortical tissues

Several other groups have reported by now avalanches:

Ribeiro et al, PLoS ONE, Public Library of Science, 2010, v. 5, p. e14129Mazzoni et al, PLoS ONE, Public Library of Science, 2007, v. 2, p. e439Shew et al, Journal of Neuroscience, 2009, v. 29, p. 15595Shew et al, Journal of Neuroscience, 2011, v. 31, p. 55

Kinouchi-Copelli model: optimal dynamic range at criticality.

We have found: optimization of dynamic range and entropy of lifetimes

Channel efficiency (= entropy of lifetimes): efficiency coding info. through firing rate

Channel efficiency always exhibit a critical optimization

2. Kinouchi-Copelli Model

N nodes connected through adjacency matrix A State of j-th node: Xj(t)

Xj = 0: quiescent Xj = 1: excited m > Xj > 1: refractory

n1

n2

n3

n4 n5

A12

A14

A24

A43

A45

A31

A53

A52

Kinouchi and Copelli, Nat. Phys., 2006

Dynamics as follows:• if 1 ≤ Xj(t) ≤ m− 2, then Xj(t + 1) = Xj(t) + 1;• if Xj(t) = m− 1, then Xj(t + 1) = 0;• if Xj(t) = 0, then Xj(t + 1) = 1 with probability

– η (external stimulus);–Ajk,∀k, by each of its neighbors.

Instantaneous mean activity:

ρ(t) =

N∑j=1

Xj(t)

Mean activity:

FT =1

T

T∑t=1

ρ(t)

Average branching ratio:

σ =

N∑j=1

1

N

N∑p=1

AjpDynamic range is an equilibrium measure.

3. Avalanches

Activity initiated by a single neuron: burst

Avalanches: critical bursts

We study distribution of size and durationof these bursts when varying σ

Size: number of neurons without repetition

Time: number of a single burst time steps

Avalanche size and lifetime are out of equilibrium measures.

Simulations run 106 bursts with N = 105, m = 10 and K ∈ {2, 5, 10, 15}.

4. Random graphs – Erdos-Rényi topology

Simulations and theory

Size exponent: -3/2

Lifetime exponent: -1.9

Shew et al, Journal of Neuroscience, 2009,

29, 15595-15600

Beggs and Plenz, The Journal of Neuro-

science, 2003, 23, 11167-11177

Mosqueiro, Akimushkin and Maia – DINCON 2011, doi: 10.5540/DINCON.2011.001.1.0064

5. Scale-free graphs – Barabási-Álbert topology

Critical point: σc = 0.4

Lower exponents in power law degree distro.:

also exhibit lack of scale invariance

Branching process analysis agree with this critical σ

Networks with several values of N were tested and nomeaningful change was detected in distributions

6. Entropy in both topologies

Similar as in Shew et al, Journal of Neuro-

science, 2011, 31, 15595

Erdos-Rényi results

Entropy of both avalanche lifetimesand sizes are optimized at criticality

Barabási-Álbert results

Entropy of avalanche lifetimes isoptimized at criticality

Dynamic range and avalanchelifetimes are both not optimized atK = 2

7. Conclusion

Summarizing, we studied the avalanches in Kinouchi-Copelli model in a first attempt to figure outdetailed mechanisms of information transmission in sensory systems. We discovered that, in acritical point, the entropy of avalanche lifetime statistics (information efficiency) is always max-imized jointly with the dynamic range, an important measure of information transmission extractedfrom the tuning curves from psychophysics. Our findings fit in the discussions regarding the roleof criticality in information processing and the relationship of long bursts of activity with thedynamic range, specially because they suggest critical behavior without pure scaleinvariance.

8. Acknowledgements

The authors would like to thank financial support from CAPES and FAPESP.

Poster powered by Fedora 14 Linux, LATEX, sciposter++, Emacs, GnuPlot and GIMP. Criticality in Neural Systems Symposium, April 30 – May 1, 2012