logging in or signing up japan Kliment Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINTLite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 56 Category: News & Reports.. License: All Rights Reserved Like it (0) Dislike it (0) Added: September 27, 2007 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript Chaos and Self-Organization in Spatiotemporal Models of Ecology: Chaos and Self-Organization in Spatiotemporal Models of Ecology J. C. Sprott Department of Physics University of Wisconsin - Madison Presented at the Eighth International Symposium on Simulation Science in Hayama, Japan on March 5, 2003Slide2: Collaborators Janine Bolliger Swiss Federal Research Institute David Mladenoff University of Wisconsin - MadisonOutline: Outline Historical forest data set Stochastic cellular automaton model Deterministic cellular automaton model Application to corrupted imagesLandscape of Early Southern Wisconsin (USA): Landscape of Early Southern Wisconsin (USA)Stochastic Cellular Automaton Model : Stochastic Cellular Automaton Model Cellular Automaton(Voter Model): Cellular Automaton (Voter Model) Cellular automaton: Square array of cells where each cell takes one of the 6 values representing the landscape on a 1-square mile resolution Evolving single-parameter model: A cell dies out at random times and is replaced by a cell chosen randomly within a circular radius r (1 < r < 10) Boundary conditions: periodic and reflecting Initial conditions: random and ordered Constraint: The proportions of land types are kept equal to the proportions of the experimental dataInitial Conditions: Random Initial Conditions Ordered Cluster Probability: A point is assumed to be part of a cluster if its 4 nearest neighbors are the same as it is. CP (Cluster probability) is the % of total points that are part of a cluster. Cluster ProbabilityCluster Probabilities (1): Cluster Probabilities (1) Random initial conditions experimental valueCluster Probabilities (2): Cluster Probabilities (2) Ordered initial conditions experimental valueFluctuations in Cluster Probability: Fluctuations in Cluster Probability r = 3 Number of generations Cluster probabilityPower Spectrum (1) : Power Spectrum (1) Power laws (1/fa) for both initial conditions; r = 1 and r = 3 Slope: a = 1.58 r = 3 Frequency Power SCALE INVARIANT Power law !Power Spectrum (2): Power Spectrum (2) Power Frequency No power law (1/fa) for r = 10 r = 10 No power lawSlide14: Fractal Dimension (1) = separation between two points of the same category (e.g., prairie) C = Number of points of the same category that are closer than e Power law: C = D (a fractal) where D is the fractal dimension: D = log C / log Slide15: Fractal Dimension (2) Simulated landscape Observed landscapeSlide16: A Measure of Complexity for Spatial Patterns One measure of complexity is the size of the smallest computer program that can replicate the pattern. A GIF file is a maximally compressed image format. Therefore the size of the file is a lower limit on the size of the program. Observed landscape: 6205 bytes Random model landscape: 8136 bytes Self-organized model landscape: 6782 bytes (r = 3) Simplified Model: Simplified Model Previous model 6 levels of tree densities nonequal probabilities randomness in 3 places Simpler model 2 levels (binary) equal probabilities randomness in only 1 place Deterministic Cellular Automaton Model : Deterministic Cellular Automaton Model Why a deterministic model?: Why a deterministic model? Randomness conceals ignorance Simplicity can produce complexity Chaos requires determinism The rules provide insightModel Fitness: Model Fitness 0 1 1 1 1 2 2 2 2 3 3 3 3 4 4 4 4 4 4 4 4 Define a spectrum of cluster probabilities (from the stochastic model): CP1 = 40.8% CP2 = 27.5% CP3 = 20.2% CP4 = 13.8% Require that the deterministic model has the same spectrum of cluster probabilities as the stochastic model (or actual data) and also 50% live cells.Update Rules: Update Rules 0 1 1 1 1 2 2 2 2 3 3 3 3 4 4 4 4 4 4 4 4 Truth Table 210 = 1024 combinations for 4 nearest neighbors 22250 = 10677 combinations for 20 nearest neighbors Totalistic ruleGenetic Algorithm: Genetic Algorithm Mom: 1100100101 Pop: 0110101100 Cross: 1100101100 Mutate: 1100101110 Keep the fittest two and repeat Slide23: Is it Fractal? Deterministic Model Stochastic Model D = 1.666 D = 1.685 0 0 0 0 3 3 -3 -3 log log e e log C( ) log C( ) e e Is it Self-organized Critical?: Is it Self-organized Critical? Frequency Power Slope = 1.9Is it Chaotic?: Is it Chaotic?Conclusions: Conclusions A purely deterministic cellular automaton model can produce realistic landscape ecologies that are fractal, self-organized, and chaotic.Application to Corrupted Images: Application to Corrupted ImagesLandscape with Missing Data: Landscape with Missing Data Single 60 x 60 block of missing cells Replacement from 8 nearest neighbors Original Corrupted CorrectedImage with Corrupted Pixels: Image with Corrupted Pixels 441 missing blocks with 5 x 5 pixels each and 16 gray levels Replacement from 8 nearest neighbors Original Corrupted Corrected Cassie Kight’s calico cat CallieMultispecies Lotka-Volterra Model with Evolution: Multispecies Lotka-Volterra Model with EvolutionMultispecies Lotka-Volterra Model with Evolution: Let Si(x,y) be density of the ith species (trees, rabbits, people, …) dSi / dt = riSi (1 - Si - Σ aijSj ) Choose ri and aij from a Poisson random distribution (both positive) Replace species that die with new ones chosen randomly Multispecies Lotka-Volterra Model with Evolution ji Evolution of Total Biomass: Evolution of Total Biomass Time BiomassConclusions: Conclusions Competitive exclusion eliminates most species. The dominant species is eventually killed and replaced by another. Evolution is punctuated rather than continual. Summary: Summary Nature is complex Simple models may suffice butReferences: References http://sprott.physics.wisc.edu/ lectures/japan.ppt (This talk) J. C. Sprott, J. Bolliger, and D. J. Mladenoff, Phys. Lett. A 297, 267-271 (2002) sprott@physics.wisc.edu You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.
japan Kliment Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINTLite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 56 Category: News & Reports.. License: All Rights Reserved Like it (0) Dislike it (0) Added: September 27, 2007 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript Chaos and Self-Organization in Spatiotemporal Models of Ecology: Chaos and Self-Organization in Spatiotemporal Models of Ecology J. C. Sprott Department of Physics University of Wisconsin - Madison Presented at the Eighth International Symposium on Simulation Science in Hayama, Japan on March 5, 2003Slide2: Collaborators Janine Bolliger Swiss Federal Research Institute David Mladenoff University of Wisconsin - MadisonOutline: Outline Historical forest data set Stochastic cellular automaton model Deterministic cellular automaton model Application to corrupted imagesLandscape of Early Southern Wisconsin (USA): Landscape of Early Southern Wisconsin (USA)Stochastic Cellular Automaton Model : Stochastic Cellular Automaton Model Cellular Automaton(Voter Model): Cellular Automaton (Voter Model) Cellular automaton: Square array of cells where each cell takes one of the 6 values representing the landscape on a 1-square mile resolution Evolving single-parameter model: A cell dies out at random times and is replaced by a cell chosen randomly within a circular radius r (1 < r < 10) Boundary conditions: periodic and reflecting Initial conditions: random and ordered Constraint: The proportions of land types are kept equal to the proportions of the experimental dataInitial Conditions: Random Initial Conditions Ordered Cluster Probability: A point is assumed to be part of a cluster if its 4 nearest neighbors are the same as it is. CP (Cluster probability) is the % of total points that are part of a cluster. Cluster ProbabilityCluster Probabilities (1): Cluster Probabilities (1) Random initial conditions experimental valueCluster Probabilities (2): Cluster Probabilities (2) Ordered initial conditions experimental valueFluctuations in Cluster Probability: Fluctuations in Cluster Probability r = 3 Number of generations Cluster probabilityPower Spectrum (1) : Power Spectrum (1) Power laws (1/fa) for both initial conditions; r = 1 and r = 3 Slope: a = 1.58 r = 3 Frequency Power SCALE INVARIANT Power law !Power Spectrum (2): Power Spectrum (2) Power Frequency No power law (1/fa) for r = 10 r = 10 No power lawSlide14: Fractal Dimension (1) = separation between two points of the same category (e.g., prairie) C = Number of points of the same category that are closer than e Power law: C = D (a fractal) where D is the fractal dimension: D = log C / log Slide15: Fractal Dimension (2) Simulated landscape Observed landscapeSlide16: A Measure of Complexity for Spatial Patterns One measure of complexity is the size of the smallest computer program that can replicate the pattern. A GIF file is a maximally compressed image format. Therefore the size of the file is a lower limit on the size of the program. Observed landscape: 6205 bytes Random model landscape: 8136 bytes Self-organized model landscape: 6782 bytes (r = 3) Simplified Model: Simplified Model Previous model 6 levels of tree densities nonequal probabilities randomness in 3 places Simpler model 2 levels (binary) equal probabilities randomness in only 1 place Deterministic Cellular Automaton Model : Deterministic Cellular Automaton Model Why a deterministic model?: Why a deterministic model? Randomness conceals ignorance Simplicity can produce complexity Chaos requires determinism The rules provide insightModel Fitness: Model Fitness 0 1 1 1 1 2 2 2 2 3 3 3 3 4 4 4 4 4 4 4 4 Define a spectrum of cluster probabilities (from the stochastic model): CP1 = 40.8% CP2 = 27.5% CP3 = 20.2% CP4 = 13.8% Require that the deterministic model has the same spectrum of cluster probabilities as the stochastic model (or actual data) and also 50% live cells.Update Rules: Update Rules 0 1 1 1 1 2 2 2 2 3 3 3 3 4 4 4 4 4 4 4 4 Truth Table 210 = 1024 combinations for 4 nearest neighbors 22250 = 10677 combinations for 20 nearest neighbors Totalistic ruleGenetic Algorithm: Genetic Algorithm Mom: 1100100101 Pop: 0110101100 Cross: 1100101100 Mutate: 1100101110 Keep the fittest two and repeat Slide23: Is it Fractal? Deterministic Model Stochastic Model D = 1.666 D = 1.685 0 0 0 0 3 3 -3 -3 log log e e log C( ) log C( ) e e Is it Self-organized Critical?: Is it Self-organized Critical? Frequency Power Slope = 1.9Is it Chaotic?: Is it Chaotic?Conclusions: Conclusions A purely deterministic cellular automaton model can produce realistic landscape ecologies that are fractal, self-organized, and chaotic.Application to Corrupted Images: Application to Corrupted ImagesLandscape with Missing Data: Landscape with Missing Data Single 60 x 60 block of missing cells Replacement from 8 nearest neighbors Original Corrupted CorrectedImage with Corrupted Pixels: Image with Corrupted Pixels 441 missing blocks with 5 x 5 pixels each and 16 gray levels Replacement from 8 nearest neighbors Original Corrupted Corrected Cassie Kight’s calico cat CallieMultispecies Lotka-Volterra Model with Evolution: Multispecies Lotka-Volterra Model with EvolutionMultispecies Lotka-Volterra Model with Evolution: Let Si(x,y) be density of the ith species (trees, rabbits, people, …) dSi / dt = riSi (1 - Si - Σ aijSj ) Choose ri and aij from a Poisson random distribution (both positive) Replace species that die with new ones chosen randomly Multispecies Lotka-Volterra Model with Evolution ji Evolution of Total Biomass: Evolution of Total Biomass Time BiomassConclusions: Conclusions Competitive exclusion eliminates most species. The dominant species is eventually killed and replaced by another. Evolution is punctuated rather than continual. Summary: Summary Nature is complex Simple models may suffice butReferences: References http://sprott.physics.wisc.edu/ lectures/japan.ppt (This talk) J. C. Sprott, J. Bolliger, and D. J. Mladenoff, Phys. Lett. A 297, 267-271 (2002) sprott@physics.wisc.edu