Abstract:Summary
1. Sexual populations are expected to perform better in fluctuating environments than asexuals because recombination provides the potential to adapt to changing environments due to increased genetic variation. Nevertheless, some asexual species show comparably high levels of genotypic diversity. Such diversity might be achieved through gene flow between coexisting sexual and asexual populations or through sexual events within asexual populations.
2. Evidence for occasional sex in the flatworm Schmidtea… Show more
“…Earlier studies in other sexual/asexual systems have shown that the frequency of sexual reproduction varies among natural populations and that the genetic signature of sexual reproduction can be seen in many predominately asexual populations (Michiels et al ., ; Bruvo et al ., ; Allen & Lynch, ; Sánchez Navarro et al ., ). However, direct comparisons of temporal variation in sexual frequency in mixed populations remain rare.…”
According to the Red Queen hypothesis for sex, parasite-mediated selection against common clones counterbalances the reproductive advantage of asexual lineages, which would otherwise outcompete sexual conspecifics. Such selection on the clonal population is expected to lead to a faster clonal turnover in habitats where selection by parasites is stronger. We tested this prediction by comparing the genetic structure of clonal and sexual populations of freshwater snail Potamopyrgus antipodarum between years 2003 and 2007 in three depth-specific habitats in Lake Alexandrina (South Island, New Zealand). These habitats differ in the risk of infection by castrating trematodes and in the relative proportion of sexual individuals. As predicted, we found that the clonal structure changed significantly in shallow and mid-water habitats, where prevalence of infection was high, but not in the deep habitat, where parasite prevalence was low. Additionally, we found that both clonal diversity and evenness of the asexual population declined in the shallow habitat. In contrast, the genetic structure (based on F-statistics) of the coexisting sexual population did not change, which suggests that the change in the clonal structure cannot be related to genetic changes in the sexual population. Finally, the frequency of sexuals had no effect on the diversity of the sympatric clonal population. Taken together, our results show a more rapid clonal turnover in high-infection habitats, which gives support for the Red Queen hypothesis for sex.
“…Earlier studies in other sexual/asexual systems have shown that the frequency of sexual reproduction varies among natural populations and that the genetic signature of sexual reproduction can be seen in many predominately asexual populations (Michiels et al ., ; Bruvo et al ., ; Allen & Lynch, ; Sánchez Navarro et al ., ). However, direct comparisons of temporal variation in sexual frequency in mixed populations remain rare.…”
According to the Red Queen hypothesis for sex, parasite-mediated selection against common clones counterbalances the reproductive advantage of asexual lineages, which would otherwise outcompete sexual conspecifics. Such selection on the clonal population is expected to lead to a faster clonal turnover in habitats where selection by parasites is stronger. We tested this prediction by comparing the genetic structure of clonal and sexual populations of freshwater snail Potamopyrgus antipodarum between years 2003 and 2007 in three depth-specific habitats in Lake Alexandrina (South Island, New Zealand). These habitats differ in the risk of infection by castrating trematodes and in the relative proportion of sexual individuals. As predicted, we found that the clonal structure changed significantly in shallow and mid-water habitats, where prevalence of infection was high, but not in the deep habitat, where parasite prevalence was low. Additionally, we found that both clonal diversity and evenness of the asexual population declined in the shallow habitat. In contrast, the genetic structure (based on F-statistics) of the coexisting sexual population did not change, which suggests that the change in the clonal structure cannot be related to genetic changes in the sexual population. Finally, the frequency of sexuals had no effect on the diversity of the sympatric clonal population. Taken together, our results show a more rapid clonal turnover in high-infection habitats, which gives support for the Red Queen hypothesis for sex.
“…In some cases, such as found in the planarian flatworm, Schmidtea polychroa , polyploid individuals can produce viable sperm that may lead to rare sexual processes (Sánchez‐Navarro et al . ). As asexually reproducing plants and animals often have uneven ploidy levels (e.g.…”
Section: Introductionmentioning
confidence: 97%
“…In the animal kingdom, the majority of polyploid invertebrates and reptiles reproduce asexually, and it has been estimated that 99% of apomictic plant species are polyploids (Suomalainen et al 1987). In some cases, such as found in the planarian flatworm, Schmidtea polychroa, polyploid individuals can produce viable sperm that may lead to rare sexual processes (S anchez-Navarro et al 2013). As asexually reproducing plants and animals often have uneven ploidy levels (e.g.…”
Despite the importance of polyploidy and the increasing availability of new genomic data, there remain important gaps in our knowledge of polyploid population genetics. These gaps arise from the complex nature of polyploid data (e.g. multiple alleles and loci, mixed inheritance patterns, association between ploidy and mating system variation). Furthermore, many of the standard tools for population genetics that have been developed for diploids are often not feasible for polyploids. This review aims to provide an overview of the state-of-the-art in polyploid population genetics and to identify the main areas where further development of molecular techniques and statistical theory is required. We review commonly used molecular tools (amplified fragment length polymorphism, microsatellites, Sanger sequencing, next-generation sequencing and derived technologies) and their challenges associated with their use in polyploid populations: that is, allele dosage determination, null alleles, difficulty of distinguishing orthologues from paralogues and copy number variation. In addition, we review the approaches that have been used for population genetic analysis in polyploids and their specific problems. These problems are in most cases directly associated with dosage uncertainty and the problem of inferring allele frequencies and assumptions regarding inheritance. This leads us to conclude that for advancing the field of polyploid population genetics, most priority should be given to development of new molecular approaches that allow efficient dosage determination, and to further development of analytical approaches to circumvent dosage uncertainty and to accommodate 'flexible' modes of inheritance. In addition, there is a need for more simulation-based studies that test what kinds of biases could result from both existing and novel approaches.
“…Second, parthenogenetic forms also harbor more infections by a presumed parasitic amoeboid protozoan, which is in some respects consistent with the Red Queen hypothesis that predicts sexuality protects against parasites, though in this case the costs of infection (required for the hypothesis to work) are unclear (Michiels et al, ). Subsequent efforts have focused on explaining the maintenance of both sexual and parthenogenetic forms, with phylogeographic and experimental evidence indicating that hybridization between the two occurs, as does genetic exchange between parthenogenetic individuals via various mechanisms that lead to the occasional retention of paternal chromosomes and exclusion of maternal chromosomes, and frequently involve transitions in ploidy (Pongratz et al, ; D'Souza et al, ; Sánchez Navarro and Jokela, ). This may help to maintain genetic diversity in parthenogens and explain their persistence.…”
SUMMARYFlatworms exhibit huge diversity in their reproductive biology, making this group an excellent model system for exploring how differences among species in reproductive ecology are reflected in the physiological and molecular details of how reproduction is achieved. In this review, I consider five key ''lifestyle choices'' (i.e., alternative evolutionary/developmental outcomes) that collectively encompass much of flatworm sexual diversity, beginning with the decisions: (i) whether to be freeliving or parasitic; (ii) whether to reproduce asexually or sexually; and (iii) whether to be gonochoristic (separate-sexed) or hermaphroditic. I then examine two further decisions involving hermaphroditism: (iv) outcrossing versus selfing and (v) the balance of investment into the male versus the female sex function (sex allocation). Collectively, these lifestyle choices set the basic rules for how reproduction occurs, but as I emphasize in the second part of the review, the reproductive biology of flatworms is also greatly impacted by the near-pervasive and powerful pressure of sexual selection, together with the related phenomena of sperm competition and sexual conflict. Exactly how this plays out, however, is strongly affected by the particular combination of reproductive strategies adopted by each species. A striking feature of flatworms . . . is the complexity and diversity of their reproductive systems.
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