|
The Consequence of Maximum Thermodynamic Efficiency in Daisyworld
|
|
0
|
340
|
February 16, 2022
|
|
“Wet/dry Daisyworld”: a conceptual tool for quantifying the spatial scaling of heterogeneous landscapes and its impact on the subgrid variability of energy fluxes
|
|
0
|
302
|
February 16, 2022
|
|
On Homeostasis in Daisyworld
|
|
0
|
327
|
February 16, 2022
|
|
One-dimensional daisyworld: spatial interactions and pattern formation
|
|
0
|
291
|
February 16, 2022
|
|
Spatio-temporal dynamics and quantification of daisyworld in two-dimensional coupled map lattices
|
|
0
|
322
|
February 16, 2022
|
|
Self-sustained temperature oscillations on Daisyworld
|
|
0
|
324
|
February 16, 2022
|
|
Homeostasis and rein control: From daisyworld to active perception
|
|
0
|
298
|
February 16, 2022
|
|
Catastrophic desert formation in Daisyworld
|
|
0
|
377
|
February 16, 2022
|
|
The Ecopoiesis of Daisy World
|
|
0
|
399
|
February 12, 2022
|
|
Chaos in daisyworld
|
|
0
|
339
|
February 12, 2022
|
|
Modeling structural change in spatial system dynamics: A Daisyworld example
|
|
0
|
301
|
February 12, 2022
|
|
Evolution without Natural Selection: Further Implications of the Daisyworld Parable
|
|
0
|
329
|
February 12, 2022
|
|
Darwinian Daisyworld
|
|
0
|
301
|
February 12, 2022
|
|
Daisyworld revisited: quantifying biological effects on planetary self-regulation
|
|
0
|
333
|
February 12, 2022
|
|
Daisyworld: A review
|
|
0
|
266
|
February 12, 2022
|
|
Daisyworld is Darwinian: Constraints on Adaptation are Important for Planetary Self-Regulation
|
|
0
|
249
|
February 12, 2022
|
|
Biological homeostasis of the global environment: the parable of Daisyworld
|
|
0
|
207
|
February 12, 2022
|
|
Open-endedness: The last grand challenge you’ve never heard of
|
|
0
|
392
|
October 6, 2021
|
|
A Model of the Mechanisms of Language Extinction and Revitalization Strategies to Save Endangered Languages
|
|
0
|
366
|
August 28, 2021
|
|
Is there a liquid state machine in the bacterium Escherichia Coli?
|
|
0
|
412
|
August 28, 2021
|
|
The neuronal replicator hypothesis
|
|
0
|
395
|
August 28, 2021
|
|
Molecular circuits for associative learning in single-celled organisms
|
|
0
|
431
|
August 28, 2021
|
|
Evolutionary potential and requirements for minimal protocells
|
|
0
|
401
|
August 28, 2021
|
|
A Stochastic Model of Nonenzymatic Nucleic Acid Replication: “Elongators” Sequester Replicators
|
|
0
|
354
|
August 28, 2021
|
|
Evolvable Neuronal Paths: A Novel Basis for Information and Search in the Brain
|
|
0
|
379
|
August 28, 2021
|
|
Primordial evolvability: Impasses and challenges
|
|
0
|
406
|
August 28, 2021
|
|
Origins and evolution of language and speech
|
|
0
|
459
|
August 28, 2021
|
|
What is comparable in comparative cognition?
|
|
0
|
413
|
August 28, 2021
|
|
Meta-learning by the Baldwin effect
|
|
0
|
417
|
August 28, 2021
|
|
Evolving intrinsic motivations for altruistic behavior
|
|
0
|
428
|
August 28, 2021
|