Mutation Accumulation and the Extinction of Small Populations

Abstract

Although extensive work has been done on the relationship between population size and the risk of extinction due to demographic and environmental stochasticity, the role of genetic deterioration in the extinction process is poorly understood. We develop a general theoretical approach for evaluating the risk of small populations to extinction via the accumulation of mildly deleterious mutations, and we support this with extensive computer simulations. Unlike previous attempts to model the genetic consequences of small population size, our approach is genetically explicit and fully accounts for the mutations inherited by a founder population as well as those introduced by subsequent mutation. Application of empirical estimates of the properties of spontaneous deleterious mutations leads to the conclusion that populations with effective sizes smaller than 100 (and actual sizes smaller than 1,000) are highly vulnerable to extinction via a mutational meltdown on timescales of approximately 100 generations. We point out a number of reasons why this is likely to be an overly optimistic view. Thus, from a purely genetic perspective, current management policies that provide formal protection to species only after they have dwindled to 100-1,000 individuals are inadequate. A doubling of the deleterious mutation rate, as can result from the release of mutagenic pollutants by human activity, is expected to reduce the longevity of a population by about 50%. As some investigators have previously suggested, the genetic load of a population can be readily purged by intentional inbreeding. However, this effect is at best transient, as intentional inbreeding can only enhance the probability of fixation of deleterious alleles, and those alleles that are purged are rapidly replaced with new mutations.