Clonality is a pervasive feature of sessile organisms, but this form of asexual reproduction is thought to interfere with sexual fitness via the movement of gametes among the modules that comprise the clone. This within-clone movement of gametes is expected to reduce sexual fitness via mate limitation of male reproductive success and, in some cases, via the production of highly inbred (i.e., self-fertilized) offspring. However, clonality also results in the spatial expansion of the genetic individual (i.e., genet), and this should decrease distances gametes and sexually produced offspring must travel to avoid competing with other gametes and offspring from the same clone. The extent to which any negative effects of clonality on mating success might be offset by the positive effects of spatial expansion is poorly understood. Here, we develop spatially explicit models in which fitness was determined by the success of genets through their male and female sex functions. Our results indicate that clonality serves to increase sexual fitness when it is associated with the outward expansion of the genet. Our models further reveal that the main fitness benefit of clonal expansion might occur through the dispersal of offspring over a wider area compared with nonclonal phenotypes. We conclude that, instead of interfering with sexual reproduction, clonal expansion should often serve to enhance sexual fitness.asexual reproduction | geitonogamy | genet | modularity | ramet M odular growth, clonality, and hermaphroditism are widespread features of sessile organisms. Sessile organisms might benefit from modularity and the spatial expansion of the individual via enhanced resource capture, and thereby improved growth and survival (1-3). However, growth and survival are only two of the key components of an organism's life history, and the third, reproduction, is the one that is most intimately linked to fitness. Indeed, during reproduction, the growth of a modular hermaphrodite might interfere with its success as a parent. In particular, it has been argued that the production of numerous partially or fully autonomous clonal modules (i.e., ramets) should interfere with mating success because there is a nonzero chance that sperm (or pollen) will encounter the receptive tissues associated with the female function of the same genetic individual (i.e., the genet). All else being equal, the larger the clone, the greater the chance that this kind of mating interference should occur (4, 5). The negative effects of such intraclonal mating is expected to occur through reductions in the number of offspring sired on other genets (i.e., outcross siring success, corresponding with the fitness of individuals via their male function) and, in self-compatible organisms, through inbreeding depression (i.e., a reduction in offspring fitness, with negative effects on the fitness of individuals through their female function; e.g., ref. 5). However, these forms of mating interference are simply by-products of attaining a larger size and are not exclusiv...