Abstract.-We investigate mate availability in different models of multiallelic self-incompatibility systems in mutationselection-drift balance in finite populations. Substantial differences among self-incompatibility systems occur in average mate availability, and in variances of mate availability among individual plants. These differences are most pronounced in small populations in which low mate availability may reduce seed set in some types of sporophytic self-incompatibility. In cases where the pollination system causes a restriction in the number of pollen genotypes available to an individual plant, the fecundity of that plant depends on the availability of compatible pollen, which is determined by its genotype at the incompatibility locus. This leads to an additional component of selection acting on selfincompatibility systems, which we term "fecundity selection." Fecundity selection increases the number of alleles maintained in finite populations and increases mate availability in small populations. The strength of fecundity selection is dependent on the type of self-incompatibility. In some cases, fecundity selection markedly alters the equilibrium dynamics of self-incompatibility alleles. We discuss the population genetic consequences of mate availability and fecundity selection in the contexts of conservation management of self-incompatible plant species and experimental investigations on self-incompatibility in natural populations.Key words.-Fecundity selection, mate availability, plant mating systems, self-incompatibility.Received May 21, 1997. Accepted September 29, 1997.A key feature of self-incompatibility (SI) systems in plants is the mate availability or proportion of compatible matings in a population (Bateman 1952;de Nettancourt 1977). A mating is the transfer of pollen from a paternally acting individual to the stigma of a maternally acting individual, and the mating is incompatible if pollen and stigma share the same phenotype with respect to SL Mate availability of an individual can therefore be defined as the likelihood that a randomly chosen mate is compatible. Darwin (1877) first noted that SI in distylous species causes each plant to be cross-sterile with "half its brethren," that is, reduces mate availability to 50%. The consequences of limited mate availability for the evolution of SI systems were discussed by Charlesworth (1988) and Lloyd and Webb (1992), and limited mate availability has been invoked in comparisons of reproductive efficiency in dioecy versus gametophytic SI (Anderson andStebbins 1984, 1994;Karoly 1994). Conservation management in endangered plant species with SI systems also involves the consideration of mate availability (e.g. Byers and Meagher 1992;DeMauro 1993;Godt and Hamrick 1995). The number of alleles maintained in small populations with multiallelic SI systems is expected to be low (Wright 1939;Imrie et al. 1972), and therefore mate availability is expected to be generally low. Low mate availability may add to a crisis by causing low seed set (Les et al. 199...