scholarly journals AEGIS: An In Silico Tool to model Genome Evolution in Age-Structured Populations

2019 ◽  
Author(s):  
William J. Bradshaw ◽  
Arian Šajina ◽  
Dario Riccardo Valenzano

AbstractAEGIS (Ageing of Evolving Genomes In Silico) is a versatile population-genetics numerical-simulation tool that enables the evolution of life history trajectories under sexual and asexual reproduction and a wide variety of evolutionary constraints. By encoding age-specific survival and reproduction probabilities as discrete genomic elements, AEGIS allows these probabilities to evolve freely and independently over time. Simulation of population evolution with AEGIS demonstrates that ageing-like phenotypes evolve in stable environments under a wide range of conditions, that life history trajectories depend heavily on mutation rates, and that sexual populations are better able to accumulate high levels of beneficial mutations affecting early-life survival and reproduction. AEGIS is free and open-source, and aims to become a standard reference tool in the study of life-history evolution and the evolutionary biology of ageing.

2009 ◽  
Vol 276 (1663) ◽  
pp. 1737-1745 ◽  
Author(s):  
Damian K. Dowling ◽  
Leigh W. Simmons

Evolutionary theory is firmly grounded on the existence of trade-offs between life-history traits, and recent interest has centred on the physiological mechanisms underlying such trade-offs. Several branches of evolutionary biology, particularly those focusing on ageing, immunological and sexual selection theory, have implicated reactive oxygen species (ROS) as profound evolutionary players. ROS are a highly reactive group of oxygen-containing molecules, generated as common by-products of vital oxidative enzyme complexes. Both animals and plants appear to intentionally harness ROS for use as molecular messengers to fulfil a wide range of essential biological processes. However, at high levels, ROS are known to exert very damaging effects through oxidative stress. For these reasons, ROS have been suggested to be important mediators of the cost of reproduction, and of trade-offs between metabolic rate and lifespan, and between immunity, sexual ornamentation and sperm quality. In this review, we integrate the above suggestions into one life-history framework, and review the evidence in support of the contention that ROS production will constitute a primary and universal constraint in life-history evolution.


2014 ◽  
Author(s):  
Ryan Baldini

I propose a method that estimates the selection response of all vital rates in an age-structured population. I assume that vital rates are determined by the additive genetic contributions of many loci. The method uses all relatedness information in the sample to inform its estimates of genetic parameters, via an MCMC Bayesian framework. One can use the results to estimate the selection response of any life history trait that is a function of the vital rates, including the age at first reproduction, total lifetime fertility, survival to adulthood, and others. This method closely ties the empirical analysis of life history evolution to dynamically complete models of natural selection, and therefore enjoys some theoretical advantages over other methods. I demonstrate the method on a simulated model of evolution with two age classes. Finally I discuss how the method can be extended to more complicated cases.


2013 ◽  
Author(s):  
Ryan Baldini

Explaining the evolution of human life history characteristics remains an outstanding problem to evolutionary anthropologists. Progress is hindered by common misunderstandings of how selection works in age-structured populations. I review two important results of life history theory related to demography. First, different life history strategies evolve under density-independent and density-dependent population growth. Second, and more poorly appreciated, different kinds of density-dependence also select for different life history strategies; assuming zero population growth alone is insufficient to determine the optimal strategy. I show that these facts are more than methodological niceties by reanalyzing the model by Kaplan et al. (2000) and showing that the results depend strongly on the form of population regulation assumed. This analysis suggests that progress in human life history theory requires better understanding of the demography of our ancestors. I close with a discussion of empirical implications.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Rogério Parentoni Martins

Concepts are linguistic structures with specific syntax and semantics used as sources of communicating ideas. Concepts can be simple (e.g., tree), complex (e.g., adaptation) and be part of a network of interactions that characterize an area of scientific research. The conceptual interrelationships and some evolutionary consequences upon which these interrelations are based will be addressed here. The evolutionary ecology is an area of research from the population evolutionary biology that deals mainly with the effect of positive natural selection on panmictic and structured populations. Environmental factors, conditions and variable resources in time and space, constitute the selective agents that act on the phenotypic and genotypic variation of populations in a single generation, could result in evolutionary adaptations, which are simply those traits that are most likely to confer survival and reproduction (evolutionary fitness) of the phenotypes that carry them in successive generations. The bases of adaptation are mainly genetic and transmitted vertically (classical Mendelian mechanisms) or horizontally (in the case of microorganisms). The phenotypic variance of the population is a conjoint consequence of the additive genotypic variance (heritability), nonadditive variance (dominance and epistasis), pleiotropy and the interaction between genotype and environment. The ability of the same genotype to respond to spatial environmental variations can result in phenotypic plasticity that manifests itself through reaction norms. The total phenotypic variation and its genetic and environmental components influence the ability of a population to evolve (evolvability).


2018 ◽  
Author(s):  
Stefano Masier ◽  
Dries Bonte

AbstractDispersal evolution impacts the fluxes of individuals and hence, connectivity in metapopulations. Connectivity is therefore decoupled from the structural connectedness of the patches within the spatial network. Because of demographic feedbacks, local selection can additionally steer the evolution of other life history traits. We investigated how different levels of connectedness affect dispersal and life history evolution by varying the interpatch distance in replicated experimental metapopulations of the two-spotted spider. We implemented a shuffling treatment to separate local- and metapopulation-level selection.With lower metapopulation connectedness, an increased starvation resistance and delayed dispersal evolved. Intrinsic growth rates evolved at the local level by transgenerational plasticity or epigenetic processes. Changes in patch connectedness thus induce the genetic and non-genetic evolution of dispersal costs and demographic traits at both the local and metapopulation level. These trait changes are anticipated to impact metapopulations eco-evolutionary dynamics, and hence, the persistence and performance of spatially structured populations.


2022 ◽  
Author(s):  
Robin S Waples

1. The Wright-Fisher model, which directs how matings occur and how genes are transmitted across generations, has long been a lynchpin of evolutionary biology. This model is elegantly simple, analytically tractable, and easy to implement, but it has one serious limitation: essentially no real species satisfies its many assumptions. With growing awareness of the importance of jointly considering both ecology and evolution in eco-evolutionary models, this limitation has become more apparent, causing many researchers to search for more realistic simulation models. 2. A recently described variation retains most of the Wright-Fisher simplicity but provides greater flexibility to accommodate departures from model assumptions. This generalized Wright-Fisher model relaxes the assumption that all individuals have identical expected reproductive success by introducing a vector of parental weights w that specifies relative probabilities different individuals have of producing offspring. With parental weights specified this way, expectations of key demographic parameters are simple functions of w. This allows researchers to quantitatively predict the consequences of non-Wright-Fisher features incorporated into their models. 3. An important limitation of the Wright-Fisher model is that it assumes discrete generations, whereas most real species are age-structured. Here I show how an algorithm (THEWEIGHT) that implements the generalized Wright-Fisher model can be used to model evolution in age-structured populations with overlapping generations. Worked examples illustrate simulation of seasonal and lifetime reproductive success and show how the user can pick vectors of weights expected to produce a desired level of reproductive skew or a desired Ne/N ratio. Alternatively, weights can be associated with heritable traits to provide a simple, quantitative way to model natural selection. Using THEWEIGHT, it is easy to generate positive or negative correlations of individual reproductive success over time, thus allowing explicit modeling of common biological processes like skip breeding and persistent individual differences. 4. R code is provided to implement basic features of THEWEIGHT and applications described here. However, required coding changes to the Wright-Fisher model are modest, so the real value of the new algorithm is to encourage users to adopt its features into their own or others models.


2021 ◽  
Author(s):  
Sébastien Lion ◽  
Sylvain Gandon

AbstractWhat is the influence of periodic environmental fluctuations on life-history evolution? We present a general theoretical framework to understand and predict the long-term evolution of life-history traits under a broad range of ecological scenarios. Indeed, this analysis yields time-varying selection gradients that help dissect the influence of the fluctuations of the environment on the competitive ability of a specific life-history mutation. We use this framework to analyse the evolution of key life-history traits of pathogens, such as transmission and virulence. These examples reveal how periodic fluctuations of the environment can affect the evolution of pathogens, and illustrate the usefulness and broad applicability of this new approach.


2019 ◽  
Vol 286 (1917) ◽  
pp. 20192187 ◽  
Author(s):  
Pat Monaghan ◽  
Neil B. Metcalfe

The idea that there is an impenetrable barrier that separates the germline and soma has shaped much thinking in evolutionary biology and in many other disciplines. However, recent research has revealed that the so-called ‘Weismann Barrier’ is leaky, and that information is transferred from soma to germline. Moreover, the germline itself is now known to age, and to be influenced by an age-related deterioration of the soma that houses and protects it. This could reduce the likelihood of successful reproduction by old individuals, but also lead to long-term deleterious consequences for any offspring that they do produce (including a shortened lifespan). Here, we review the evidence from a diverse and multidisciplinary literature for senescence in the germline and its consequences; we also examine the underlying mechanisms responsible, emphasizing changes in mutation rate, telomere loss, and impaired mitochondrial function in gametes. We consider the effect on life-history evolution, particularly reproductive scheduling and mate choice. Throughout, we draw attention to unresolved issues, new questions to consider, and areas where more research is needed. We also highlight the need for a more comparative approach that would reveal the diversity of processes that organisms have evolved to slow or halt age-related germline deterioration.


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