Genetics, Vol. 166, 1529-1539, March 2004, Copyright © 2004

The Effective Size of Mixed Sexually and Asexually Reproducing Populations

Katsuei Yonezawaa, Takuro Ishiib, and Tsukasa Nagamineb
a Department of Biotechnology, Kyoto Sangyo University, Kyoto 603-8555, Japan
b Research Team of Plant Resources, National Institute of Agrobiological Sciences, Tsukuba 305-8602, Japan

Corresponding author: Katsuei Yonezawa, Kyoto Sangyo University, Kamigamo, Kita-ku, Kyoto 603-8555, Japan., yonezaw{at}cc.kyoto-su.ac.jp (E-mail)

Communicating editor: T. H. D. BROWN

Using the transition matrix of inbreeding and coancestry coefficients, the inbreeding (NeI), variance (NeV), and asymptotic (Ne{lambda}) effective sizes of mixed sexual and asexual populations are formulated in terms of asexuality rate ({delta}), variance of asexual (C) and sexual (K) reproductive contributions of individuals, correlation between asexual and sexual contributions ({rho}ck), selfing rate (ß), and census population size (N). The trajectory of NeI toward Ne{lambda} changes crucially depending on {delta}, N, and ß, whereas that of NeV is rather consistent. With increasing asexuality, Ne{lambda} either increases or decreases depending on C, K, and {rho}ck. The parameter space in which a partially asexual population has a larger Ne{lambda} than a fully sexual population is delineated. This structure is destroyed when N(1 – {delta}) < 1 or {delta} > 1 – 1/N. With such a high asexuality, tremendously many generations are required for the asymptotic size Ne{lambda} to be established, and Ne{lambda} is extremely large with any value of C, K, and {rho}ck because the population is dominated eventually by individuals of the same genotype and the allelic diversity within the individuals decays quite slowly. In reality, the asymptotic state would occur only occasionally, and instantaneous rather than asymptotic effective sizes should be practical when predicting evolutionary dynamics of highly asexual populations.