scholarly journals Evolution in the weak-mutation limit: Stasis periods punctuated by fast transitions between saddle points on the fitness landscape

2021 ◽  
Vol 118 (4) ◽  
pp. e2015665118
Author(s):  
Yuri Bakhtin ◽  
Mikhail I. Katsnelson ◽  
Yuri I. Wolf ◽  
Eugene V. Koonin

A mathematical analysis of the evolution of a large population under the weak-mutation limit shows that such a population would spend most of the time in stasis in the vicinity of saddle points on the fitness landscape. The periods of stasis are punctuated by fast transitions, in lnNe/s time (Ne, effective population size; s, selection coefficient of a mutation), when a new beneficial mutation is fixed in the evolving population, which accordingly moves to a different saddle, or on much rarer occasions from a saddle to a local peak. Phenomenologically, this mode of evolution of a large population resembles punctuated equilibrium (PE) whereby phenotypic changes occur in rapid bursts that are separated by much longer intervals of stasis during which mutations accumulate but the phenotype does not change substantially. Theoretically, PE has been linked to self-organized criticality (SOC), a model in which the size of “avalanches” in an evolving system is power-law-distributed, resulting in increasing rarity of major events. Here we show, however, that a PE-like evolutionary regime is the default for a very simple model of an evolving population that does not rely on SOC or any other special conditions.

2020 ◽  
Author(s):  
Yuri Bakhtin ◽  
Mikhail I. Katsnelson ◽  
Yuri I. Wolf ◽  
Eugene V. Koonin

AbstractPunctuated equilibrium is a mode of evolution in which phenetic change occurs in rapid bursts that are separated by much longer intervals of stasis during which mutations accumulate but no major phenotypic change occurs. Punctuated equilibrium has been originally proposed within the framework of paleobiology, to explain the lack of transitional forms that is typical of the fossil record. Theoretically, punctuated equilibrium has been linked to self-organized criticality (SOC), a model in which the size of ‘avalanches’ in an evolving system is power-law distributed, resulting in increasing rarity of major events. We show here that, under the weak-mutation limit, a large population would spend most of the time in stasis in the vicinity of saddle points in the fitness landscape. The periods of stasis are punctuated by fast transitions, in lnNe time (Ne, effective population size), when a new beneficial mutation is fixed in the evolving population, which moves to a different saddle, or on much rarer occasions, from a saddle to a local peak. Thus, punctuated equilibrium is the default mode of evolution under a simple model that does not involve SOC or other special conditions.SignificanceThe gradual character of evolution is a key feature of the Darwinian worldview. However, macroevolutionary events are often thought to occur in a non-gradualist manner, in a regime known as punctuated equilibrium, whereby extended periods of evolutionary stasis are punctuated by rapid transitions between states. Here we analyze a mathematical model of population evolution on fitness landscapes and show that, for a large population in the weak-mutation limit, the process of adaptive evolution consists of extended periods of stasis, which the population spends around saddle points on the landscape, interrupted by rapid transitions to new saddle points when a beneficial mutation is fixed. Thus, punctuated equilibrium appears to be the default regime of biological evolution.


2021 ◽  
Author(s):  
Yipei Guo ◽  
Ariel Amir

Adaptation dynamics on fitness landscapes is often studied theoretically in the strong-selection, weak-mutation (SSWM) regime. However, in a large population, multiple beneficial mutants can emerge before any of them fixes in the population. Competition between mutants is known as clonal interference, and how it affects the form of long-term fitness trajectories in the presence of epistasis is an open question. Here, by considering how changes in fixation probabilities arising from weak clonal interference affect the dynamics of adaptation on fitness-parameterized landscapes, we find that the change in the form of fitness trajectory arises only through changes in the supply of beneficial mutations (or equivalently, the beneficial mutation rate). Furthermore, a depletion of beneficial mutations as a population climbs up the fitness landscape can speed up the functional form of the fitness trajectory, while an enhancement of the beneficial mutation rate does the opposite of slowing down the form of the dynamics. Our findings suggest that by carrying out evolution experiments in both regimes (with and without clonal interference), one could potentially distinguish the different sources of macroscopic epistasis (fitness effect of mutations vs. change in fraction of beneficial mutations).


Author(s):  
M. E. J. Newman ◽  
R. G. Palmer

The models discussed in the last chapter are intriguing, but present a number of problems. In particular, most of the results about them come from computer simulations, and little is known analytically about their properties. Results such as the power-law distribution of extinction sizes and the system's evolution to the "edge of chaos" are only as accurate as the simulations in which they are observed. Moreover, it is not even clear what the mechanisms responsible for these results are, beyond the rather general arguments that we have already given. In order to address these shortcomings, Bak and Sneppen (1993; Sneppen et al. 1995; Sneppen 1995; Bak 1996) have taken Kauffman's ideas, with some modification, and used them to create a considerably simpler model of large-scale coevolution which also shows a power-law distribution of avalanche sizes and which is simple enough that its properties can, to some extent, be understood analytically. Although the model does not directly address the question of extinction, a number of authors have interpreted it, using arguments similar to those of section 1.2.2.5, as a possible model for extinction by biotic causes. The Bak-Sneppen model is one of a class of models that show "self-organized criticality," which means that regardless of the state in which they start, they always tune themselves to a critical point of the type discussed in section 2.4, where power-law behavior is seen. We describe self-organized criticality in more detail in section 3.2. First, however, we describe the Bak-Sneppen model itself. In the model of Bak and Sneppen there are no explicit fitness landscapes, as there are in NK models. Instead the model attempts to mimic the effects of landscapes in terms of "fitness barriers." Consider figure 3.1, which is a toy representation of a fitness landscape in which there is only one dimension in the genotype (or phenotype) space. If the mutation rate is low compared with the time scale on which selection takes place (as Kauffman assumed), then a population will spend most of its time localized around a peak in the landscape (labeled P in the figure).


1996 ◽  
Vol 07 (05) ◽  
pp. 705-715 ◽  
Author(s):  
JAN FINJORD

The two-parent reproduction model of Derrida and Peliti is simulated on a rugged fitness landscape. Fixed fitness values for each possible genotype are assigned randomly, with all fit individuals having the same probability of reproduction. The previously observed transition to a self-organized state of the population with less recombinational load, implies an abrupt change of genetic overlap distributions, showing up characteristics of a phase transition. A crossover variant of the model has a smoother transition to the adapted regime, with a residual collective adaptation for small values of the threshold in fitness. When a geographical constraint (shortest possible distance) on pairwise reproduction in a population arranged one-dimensionally is imposed, a poised state results, suggestive of self-organized criticality.


2019 ◽  
Vol 42 ◽  
Author(s):  
Lucio Tonello ◽  
Luca Giacobbi ◽  
Alberto Pettenon ◽  
Alessandro Scuotto ◽  
Massimo Cocchi ◽  
...  

AbstractAutism spectrum disorder (ASD) subjects can present temporary behaviors of acute agitation and aggressiveness, named problem behaviors. They have been shown to be consistent with the self-organized criticality (SOC), a model wherein occasionally occurring “catastrophic events” are necessary in order to maintain a self-organized “critical equilibrium.” The SOC can represent the psychopathology network structures and additionally suggests that they can be considered as self-organized systems.


2020 ◽  
Vol 75 (5) ◽  
pp. 398-408
Author(s):  
A. Y. Garaeva ◽  
A. E. Sidorova ◽  
N. T. Levashova ◽  
V. A. Tverdislov

Author(s):  
M. E. J. Newman ◽  
R. G. Palmer

Developed after a meeting at the Santa Fe Institute on extinction modeling, this book comments critically on the various modeling approaches. In the last decade or so, scientists have started to examine a new approach to the patterns of evolution and extinction in the fossil record. This approach may be called "statistical paleontology," since it looks at large-scale patterns in the record and attempts to understand and model their average statistical features, rather than their detailed structure. Examples of the patterns these studies examine are the distribution of the sizes of mass extinction events over time, the distribution of species lifetimes, or the apparent increase in the number of species alive over the last half a billion years. In attempting to model these patterns, researchers have drawn on ideas not only from paleontology, but from evolutionary biology, ecology, physics, and applied mathematics, including fitness landscapes, competitive exclusion, interaction matrices, and self-organized criticality. A self-contained review of work in this field.


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