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We follow up on a companion work that considered growth rates of populations growing at different sites, with different randomly varying growth rates at each site, in the limit as migration between sites goes to 0. We extend this work here to the special case where the maximum average log growth rate is achieved at two different sites. The primary motivation is to cover the case where `sites are understood as age classes for the same individuals. The theory then calculates the effect on growth rate of introducing a rare delay in development, a diapause, into an otherwise fixed-length semelparous life history. Whereas the increase in stochastic growth rate due to rare migrations was found to grow as a power of the migration rate, we show that under quite general conditions that in the diapause model --- or in the migration model with two or more sites having equal individual stochastic growth rates --- the increase in stochastic growth rate due to diapause at rate $epsilon$ behaves like $(log epsilon^{-1})^{-1}$ as $epsilondownarrow 0$. In particular, this implies that a small random disruption to the deterministic life history will always be favored by natural selection, in the sense that it will increase the stochastic growth rate relative to the zero-delay deterministic life history.
The growth of a population divided among spatial sites, with migration between the sites, is sometimes modelled by a product of random matrices, with each diagonal elements representing the growth rate in a given time period, and off-diagonal element
The growth of a population divided among spatial sites, with migration between the sites, is sometimes modelled by a product of random matrices, with each diagonal elements representing the growth rate in a given time period, and off-diagonal element
Empirical observations show that ecological communities can have a huge number of coexisting species, also with few or limited number of resources. These ecosystems are characterized by multiple type of interactions, in particular displaying cooperat
We propose an alternative to the prevailing two origin of life narratives, one based on a replicator first hypothesis, and one based on a metabolism first hypothesis. Both hypotheses have known difficulties: All known evolvable molecular replicators
Inference with population genetic data usually treats the population pedigree as a nuisance parameter, the unobserved product of a past history of random mating. However, the history of genetic relationships in a given population is a fixed, unobserv