Cosexual Populations Research Articles

Molecular evidence for recent divergence of X- and Y-linked gene pairs in Spinacia oleracea L.

Dioecy has evolved recently and independently from cosexual populations in many angiosperm lineages, providing opportunities to understand the evolutionary process underlying this transition. Spinach (Spinacia oleracea) is a dioecious plant with homomorphic sex chromosomes (XY). Although most of the spinach Y chromosome recombines with the X chromosome, a region around the male-determining locus on Y does not recombine with its X counterpart, suggesting that this region might be related to the evolution of dioecy in the species. To identify genes located in the non-recombining region (MSY, male-specific region of Y), RNA-seq analysis of male and female progeny plants (eight each) from a sib-cross of a dioecious line was performed. We discovered only 354 sex-chromosomal SNPs in 219 transcript sequences (genes). We randomly selected 39 sex-chromosomal genes to examine the reproducibility of the RNA-seq results and observed tight linkage to the male-determining locus in a spinach segregating population (140 individuals). Further analysis using a large-scale population (>1400) and over 100 spinach germplasm accessions and cultivars showed that SNPs in at least 12 genes are fully linked to the male-determining locus, suggesting that the genes reside in the spinach MSY. Synonymous substitution rates of the MSY genes and X homologues predict a recent divergence (0.40 ± 0.08 Mya). Furthermore, synonymous divergence between spinach and its wild relative (S. tetrandra), whose sex chromosomes (XY) originated from a common ancestral chromosome, predicted that the species diverged around 5.7 Mya. Assuming that dioecy in Spinacia evolved before speciation within the genus and has a monophyletic origin, our data suggest that recombination around the spinach sex-determining locus might have stopped significantly later than the evolution of dioecy in Spinacia.

Floral size and shape evolution following the transition to gender dimorphism.

Floral morphology is expected to evolve following the transition from cosexuality to gender dimorphism in plants, as selection through male and female function becomes dissociated. Specifically, male-biased dimorphism in flower size can arise through selection for larger flowers through male function, selection for smaller flowers through female function, or both. The evolutionary pathway to floral dimorphism can be most effectively reconstructed in species with intraspecific variation in sexual system. We examined the evolution of flower size and shape in Lycium californicum, whose populations are either gender dimorphic with male and female plants, or cosexual with hermaphroditic plants. Floral morphology was characterized in populations spanning the species' complete range. For a subset of the range where cosexual and dimorphic populations are in close proximity, we compared the size and shape of flowers from female and male plants in dimorphic populations to hermaphrodites in cosexual populations, accounting for variation associated with abiotic environmental conditions. The magnitude of flower size dimorphism varied across dimorphic populations. After controlling for environmental variation across cosexual and dimorphic populations, flowers on males were larger than flowers on females and hermaphrodites, whereas flower size did not differ between females and hermaphrodites. Flower shape differences were associated with mating type, sexual system, and environmental variation. While abiotic environmental gradients shape both overall flower size and shape, male-biased flower size dimorphism in L. californicum appears to arise through selection for larger flowers in males but not smaller flowers in females.

Correlated polymorphism in cytotype and sexual system within a monophyletic species, Lycium californicum.

Polyploidy has important effects on reproductive systems in plants and has been implicated in the evolution of dimorphic sexual systems. In particular, higher ploidy is associated with gender dimorphism across Lycium species (Solanaceae) and across populations within the species Lycium californicum. Previous research on the association of cytotype and sexual system within L. californicum sampled a limited portion of the species range, and did not investigate evolutionary transitions between sexual systems. Lycium californicum occurs in arid regions on offshore islands and mainland regions in the south-western United States and Mexico, motivating a more comprehensive analysis of intraspecific variation in sexual system and cytotype across the full range of this species. Sexual system (dimorphic vs. cosexual) was determined for 34 populations across the geographical range of L. californicum using field observations of pollen production, and was confirmed using morphological measurements and among-plant correlations of primary sexual traits. Ploidy was inferred using flow cytometry in 28 populations. DNA sequence data from four plastid and two nuclear regions were used to reconstruct relationships among populations and to map transitions in sexual system and ploidy. Lycium californicum is monophyletic, ancestrally diploid and cosexual, and the association of gender dimorphism and polyploidy appears to have two evolutionary origins in this species. Compared with cosexual populations, dimorphic populations had bimodal anther size distributions, negative correlations between male and female floral traits, and larger coefficients of variation for primary sexual traits. Flow cytometry confirmed tetraploidy in dimorphic populations, whereas cosexual populations were diploid. Tetraploidy and gender dimorphism are perfectly correlated in L. californicum, and the distribution of tetraploid-dimorphic populations is restricted to populations in Arizona and the Baja California peninsula. The analysis suggests that tetraploidy and dimorphism likely established in Baja California and may have evolved multiple times.

Intraspecific variation in gender strategies in Lycium (Solanaceae): associations with ploidy and changes in floral form following the evolution of gender dimorphism.

• An association between polyploidy and gender dimorphism has been noted in several plant lineages. Whereas the majority of Lycium species are diploid and have hermaphroditic flowers in cosexual populations, gender dimorphism (gynodioecy, dioecy) has been shown to be uniformly associated with polyploidy in previous studies. Preliminary field observations suggested that some populations of Lycium carolinianum were dimorphic, providing a test of this association.• We assessed sexual systems and cytotype variation (to infer ploidy) across 17 populations of L. carolinianum. Comparison of flowers in cosexual and dimorphic populations were used to infer changes in reproductive morphology associated with the evolution of gynodioecy.• The majority of populations were cosexual in gender expression, but dimorphism was present in the Yucatán and in some populations in Hawaii. Populations varied in ploidy and were either diploid or tetraploid. Floral sexual dimorphism was present in all gynodioecious populations, though the magnitude differed and was cryptic in some cases. Our results are consistent with the hypothesis that following the evolution of gynodioecy, flowers on hermaphrodites increased in size.• Dimorphic sexual systems have likely evolved convergently in L. carolinianum. In contrast to previous studies, dimorphism is not perfectly associated with polyploidy. Although our sample from the Yucatán was both tetraploid and dimorphic, all populations in Hawaii were diploid regardless of sexual system. Ongoing phylogeographic and mating system studies will contribute to our understanding of reproductive evolution in this widespread, polymorphic species.

Gender plasticity and sexual system stability in Wurmbea

Sexually dimorphic populations are often located in drier habitats than cosexual populations. Gender plasticity (GP), whereby hermaphrodites alter female and male functions depending on resources, and sex-differential plasticity (SDP) between hermaphrodites and unisexuals are predicted to affect sexual system stability. Here, GP and SDP are evaluated in cosexual and gynodioecious Wurmbea biglandulosa and sub-dioecious and dioecious W. dioica. GP was evaluated under two resource conditions, compared among sexual systems and assessed as to whether (1) males produced perfect flowers and (2) hermaphrodites altered investment in perfect (female function) and total (male function) flowers. SDP was assessed within sexual systems as differences between sex functions of hermaphrodites vs. unisexuals. Males and hermaphrodites were compared to assess whether size thresholds for female function differed among sexual systems. Plasticity costs were evaluated using correlations between female function and male traits in hermaphrodites, and in W. dioica by comparing hermaphrodite and male regressions between plant size and pollen production. In dioecious W. dioica no males exhibited GP, whereas 100 % did in gynodioecious and cosexual W. biglandulosa. In sub-dioecious W. dioica, resources affected GP (high, 66 %; low, 42 %). Hermaphrodites in all sexual systems reduced perfect but not total flowers under low resources. Unisexuals were unaffected, demonstrating SDP for female function only. Thresholds for female function were greater in sub-dioecious W. dioica than in W. biglandulosa. Plasticity costs were detected only in sub-dioecious W. dioica. SDP for female function could assist female establishment in cosexual populations and maintain females in gynodioecious and sub-dioecious populations. Although the absence of male SDP should stabilize sub-dioecy, plasticity costs would render sub-dioecy unstable, favouring canalized males over hermaphrodites. This study highlights the importance of interactions between environmental conditions and hermaphrodite sex expression for the stability of dimorphic sexual systems.

Sex in advertising: dioecy alters the net benefits of attractiveness in Sagittaria latifolia (Alismataceae).

The flowers and inflorescences of animal-pollinated dioecious plants are generally small and inconspicuous in comparison with outcrossing cosexual species. The net benefits of an attractive floral display may be different for dioecious compared to cosexual populations because dioecious species experience a more severe reduction in pollen delivery when pollinators forage longer on fewer individuals. Here, we develop a model that predicts the decrease in pollen delivery in dioecious relative to cosexual populations from female-female, female-male and male-male visit sequences as the number of individuals visited varies. To evaluate the predictions of our model we conducted a common garden experiment with dioecious and monoecious (cosexual) arrays of the insect-pollinated herb Sagittaria latifolia. We find that, although increasing the advertisements of floral rewards (i.e. increasing floral display) attracts more pollinators to individuals, the probability that these pollinators subsequently deliver pollen to neighbouring plants depends on sexual system. Because the number of individual plants visited per foraging trip did not increase significantly with floral display, the relative pollination success of dioecious versus monoecious populations decreases with increased floral display. We propose that this could explain why dioecy is strongly correlated with reduced floral display among angiosperm species.

Environmental stress and the evolution of dioecy: Wurmbea dioica (Colchicaceae) in Western Australia

Stressful ecological conditions have been implicated in the evolution of separate sexes in plants. Gender dimorphic species are often found in drier habitats than their sexually monomorphic relatives, and gynodioecious populations appear closer to a dioecious state as resources, particularly water, become limiting. This pattern could result if dry conditions decrease the relative seed fitness of cosexual plants, allowing female plants to become established in monomorphic populations. We studied geographical variation in gender expression and biomass allocation among 12 monomorphic and dimorphic populations of Wurmbea dioica along a latitudinal precipitation gradient in southwestern Australia to provide insight into mechanisms by which aridity might favor transitions between sexual systems. Plants in monomorphic and dimorphic populations exhibited contrasting gender expression and patterns of biomass allocation in areas with different levels of precipitation. Among dimorphic populations, lower precipitation was associated with a higher frequency of female plants, and reduced allocation to female function by hermaphrodites during flowering. In contrast, stress conditions had no effect on female allocation at flowering in monomorphic populations. Across latitudes, unisexuals and cosexuals exhibited consistent differences in above ground traits, with cosexuals having larger leaves, taller stems and larger flowers. Although all plants were smaller under drier conditions, cosexuals decreased above ground allocation to vegetative and reproductive structures with decreasing latitude. In contrast, unisexuals increased allocation to reproduction in drier areas at the expense of below ground size. Aridity was associated with reduced flower size among all gender classes, but not with changes in flower number. These data do not support the hypothesis that resource limitation of female allocation in cosexual populations favors the establishment of gender dimorphism in W. dioica. Alternative hypotheses, involving higher selfing rates and enhanced survival of unisexuals relative to cosexuals under resource-limited conditions, are discussed as possible explanations for the origin of dioecy in W. dioica.

The transition to gender dimorphism on an evolutionary background of self‐incompatibility: an example from Lycium (Solanaceae)

Populations of three North American species of Lycium (Solanaceae) are morphologically gynodioecious and consist of male-sterile (i.e., female) and hermaphroditic plants. Marked individuals were consistent in sexual expression across years and male sterility was present throughout much of the species' ranges. Controlled pollinations reveal that L. californicum, L. exsertum, and L. fremontii are functionally dioecious. Fruit production in females ranged from 36 to 63%, whereas hermaphrodites functioned essentially as males. Though hermaphrodites were mostly male, investigation of pollen tube growth reveals that hermaphrodites of all dimorphic species were self-compatible. Self-fertilization and consequent inbreeding depression are commonly invoked as important selective forces promoting the invasion of male-sterile mutants into cosexual populations. A corollary prediction of these models is that gender dimorphism evolves from self-compatible ancestors. However, fruit production, seed production, and pollen tube number following outcross pollination were significantly higher than following self-pollination for three diploid, cosexual species that are closely related to the dimorphic species. The data presented here on incompatibility systems are consistent with the hypothesis that polyploidy disrupted the self-incompatibility system in the gynodioecious species leading to the evolution of gender dimorphism.

Selection by parasites for clonal diversity and mixed mating

On theoretical grounds, coevolutionary interactions with parasites can select for cross-fertilization, even when there is a twofold advantage gained by reproducing through uniparental means. The suspected advantage of cross-fertilization stems from the production of genetically rare offspring, which are expected to be more likely to escape infection by coevolving enemies. In the present study, we consider the effects that parasites have on parthenogenetic mutants in obligately sexual, dioecious populations. Computer simulations show that repeated mutation to parthenogenesis can lead to the accumulation of clones with different resistance genotypes, and that a moderately diverse set of clones could competitively exclude the ancestral sexual subpopulation. The simulations also show that, when there are reasonable rates of deleterious mutation, Muller’s ratchet combined with coevolutionary interactions with parasites can lead to the evolutionary stability of cross-fertilization. In addition, we consider the effects that parasites can have on the evolution of uniparental reproduction in cosexual populations. Strategy models show that parasites and inbreeding depression could interact to select for evolutionarily stable reproductive strategies that involve mixtures of selfed and outcrossed progeny.

VARIATION IN SEX EXPRESSION IN CANADA YEW (TAXUS CANADENSIS)

Sex expression was measured in several Canada yew (Taxus canadensis Marsh.) populations of the Apostle Islands of Wisconsin and southeastern Minnesota to determine the extent of variation within and among populations. Sex expression was recorded qualitatively (monoecious, male, or female) and quantitatively (by male to female strobilus ratios or standardized phenotypic gender). No discernible trends in differences in sex expression among populations or habitats were recorded. Trends in sex expression of individuals within populations were complex. Small yews tended to be male or, if monoecious, had female‐biased strobilus ratios. Large yews were monoecious but had male‐biased strobilus ratios. Phenotypic gender, recorded as relative maleness, however, was negatively, but weakly, correlated with plant size. Gender distribution in four of five populations was bimodal, suggesting that cosexual populations consist of male and female morphs. Strobilus ratios of individuals in Apostle Island populations showed significant annual variation, but gender for these same plants was significantly correlated from year to year. Annual adjustments in gender were most pronounced in small yews. The results indicate that relative investment in male and female reproductive structures by Canada yew individuals is responsive to environmental variation, but sex expression also has a proximate genetic component.

Selection of Combined Versus Separate Sexes in Seed Plants

In the majority of the populations of seed plants, there is a single morph, a cosex, which combines maternal and paternal functions in the same individuals. Fewer than 10% of populations are dimorphic, with differentiated males and females specializing in one sexual function. Evolution of sex conditions has been principally from cosexuality to separate sexes. Conditions under which unisexual mutants invade cosexual populations are examined. The advantages of cosexuality include the facilitation of mating, reproductive economies, noninterchangeable diminishing returns imposed on paternal and maternal fitness by Bateman's Principle and the distinct spatial distribution of maternally and paternally derived offspring, and bet-hedging. Females and males share an ability to reproduce more efficiently than cosexes under certain conditions. Females (but not males) may gain benefits from increased outcrossing, or they may gain better seed dispersal of their more massive crops, while males can conceivably obtain ...