被子植物镜像花柱及其进化意义

镜像花柱是指花柱在花水平面上向左(左花柱型)或向右(右花柱型)偏离花中轴线,是一种花柱多态现象,可根据左、右花柱花在植株上的排列式样划分为单型镜像花柱和二型镜像花柱两类,或根据镜像花柱和雄蕊的排列方式划分为雌雄互补镜像花柱和非雌雄互补镜像花柱两类。镜像花柱现象已在被子植物11个科的部分种类中进行了报道,它在保护功能型雄蕊和雌蕊、通过自交产生繁殖保障效应以及通过减小雌雄功能间干扰、提高异交率和雄性适合度等方面具有重要的进化意义,目前已成为植物繁殖生物学领域的研究热点。本文总结分析了国际上有关镜像花柱的研究工作,重点介绍:(1)镜像花柱的类型、镜像花的形态分化及花部特征,(2)镜像花柱植物在被子植物中的分布及其遗传演化,(3)镜像花的交配式样和交配频率、传粉特点及其进化生物学意义,并对今后的研究方向进行了展望,以期为进一步研究镜像花柱植物的进化生物学特性,推动我国在该领域的发展提供科学依据。     

The development of enantiostyly

Enantiostyly, the deflection of the style either to the left (left-styled) or right (right-styled) side of the floral axis, has evolved in at least ten angiosperm families. Two types of enantiostyly occur: monomorphic enantiostyly, in which individuals exhibit both stylar orientations, and dimorphic enantiostyly, in which the two stylar orientations occur on separate plants. To evaluate architectural or developmental constraints on the evolution of both forms of enantiostyly, we examined inflorescence structure and floral development among unrelated enantiostylous species. We investigated relations between the position of left- and right-styled flowers and inflorescence architecture in four monomorphic enantiostylous species, and we examined the development of enantiostyly in nine monomorphic and dimorphic enantiostylous species from five unrelated lineages. The location of left- and right-styled flowers within inflorescences ranged from highly predictable (in Solanum rostratum) to random (in Heteranthera mexicana). There were striking differences among taxa in the timing of stylar bending. In Wachendorfia paniculata, Dilatris corymbosa, and Philydrum lanuginosum, the style deflected in the bud, whereas in Heteranthera spp., Monochoria australasica, Cyanella lutea, and Solanum rostratum, stylar bending occurred at the beginning of anthesis. Comparisons of organ initiation and development indicated that asymmetries along the left-right axis were expressed very late in development, despite the early initiation of a dorsiventral asymmetry. We suggest that the evolution of dimorphic enantiostyly from monomorphic enantiostyly may be constrained by a lack of left-right positional information in the bud.     

Mirror image flowers and their effect on outcrossing rate in Chamaecrista fasciculata (Leguminosae)

The influence of enantiostyly (reciprocal segregation of anthers and stigmas to different sides of the flower) on outcrossing rate was examined in Chamaecrista fasciculata (Leguminosae). I hypothesized that enantiostyly has not evolved to increase the female component of outcrossing and actually acts to increase the selling rate through geitonogamy. To quantify the role of enantiostyly to outcrossing, plants of known isozyme genotype were manipulated to be either completely left- or right-styled (nonenantiostylous) or to have equal numbers of left- and right-styled flowers (enantiostylous). Flower number was varied to quantify any interaction between floral display size and enantiostyly on outcrossing rate. These “target” plants were surrounded by unmanipulated plants homozygous for the alternative allele. Outcrossing rates of the target plants were determined by scoring the presence or absence of heterozygotes. The contribution of enantiostyly to geitonogamy may be reduced if pollinators discriminate among the floral types. Thus, observations of pollinator movement between flowers on the same plant were made to determine if pollinators discriminate between the floral types. Although pollinators moved randomly between flower types, outcrossing rate was only marginally effected by the presence of enantiostyly. Enantiostylous plants outcrossed at a slightly lower rate than nonenantiostylous plants only when the opportunity for geitonogamy was great. These results suggest that the contribution of enantiostyly to selling is minimal.     

Variation in daily floral display and the potential for geitonogamous pollination in two monomorphic enantiostylous Monochoria species

Mirror-image flowers (enantiostyly) have long been considered a mechanism to promote cross-pollination between flowers of alternate stylar orientation. However, in monomorphic enantiostyly, the occurrence of both left- and right-styled flowers on the same individual plant might appear to promote geitonogamy rather than outcrossing relative to the condition of dimorphic enantiostyly. We investigated daily floral display during the flowering season in two experimental populations of monomorphic enantiostylous species, Monochoria korsakowii and Monochoria vaginalis (Pontederiaceae) to assess the potential effects of floral display on geitonogamous pollination. The left- and right-styled flowers exhibited a 1:1 ratio both within individuals and populations. In M. korsakowii and M. vaginalis, 86.0% and 71.3% daily floral displays involved fewer than three flowers thus reducing the likelihood of geitonogamy. Moreover, daily displays often involved one floral form and mixed-formed with unequal ratios of left- and right-styled flowers also reducing opportunities for geitonogamy. Therefore variation in daily floral display in these two Monochoria species suggests that the impact of monomorphic enantiostyly in promoting geitonogamy will be reduced by small display sizes, or through simulating dimorphic enantiostyly.     

Inheritance of apospory in bahiagrass,Paspalum notatum

Previous studies on the inheritance of aposporous apomixis in bahiagrass showed a wide range of segregation ratios in crosses involving sexual and aposporous apomictic plants. The F1 progenies were classified through a visual progeny test carried out on few F2 plants. The number of sexual F1s highly exceeded the apomictics leading to the conclusion that apomixis was controlled by a few recessive genes. The present study examines the inheritance of apospory in bahiagrass. A sexual plant was self-pollinated and crossed with an aposporous apomictic plant as pollen donor. Backcross and F2 progenies were obtained in several combinations. All self-pollinated sexual plants or sexual x sexual crosses produced progenies free of apospory. All crosses involving a sexual and an apomictic plant produced approximately three times more apospory-free plants than plants with apospory. Bahiagrass is of autotetraploid origin and hence is expected to display tetrasomic inheritance. The most widely accepted genetic model for inheritance of apospory in tropical grasses is a single dominant gene with tetrasomic inheritance. In the present experiments none of the apospory-free F1s segregated for the apospory trait indicating that it is most likely a dominant character. However, the observed results fit better a modified model: tetrasomic inheritance of a single dominant gene with pleiotropic effect and incomplete penetrance. The excess of apospory-free plants in the F1 progeny could be ascribed to some distortion in the segregation pattern due to a pleiotropic lethal effect of the dominant A allele with incomplete penetrance. Alternatively, partial lethality of factors linked to aposporous gene may account for segregation distortion against apospory.     

The genetic basis of naturally occurring pollen color dimorphisms in Nigella degenii (Ranunculaceae)

Nigella degenii ssp. barbro and ssp. jenny differ from related taxa in being dimorphic for pollen color, with some plants having dark pollen and others light pollen. In this study we performed experimental crosses to determine whether the difference in pollen color is governed by few or many loci and whether the two subspecies utilize the same gene to control pollen color. Patterns of segregation in crosses between morphs show that dark pollen is dominant over light pollen and that a single major gene is responsible for most of the variation in pollen color. Consequently it should be relatively easy for pollen color dimorphisms to establish and spread in these subspecies. Aberrant segregation ratios were attributed to genetic factors that reduced the expression of the allele conferring dark pollen or processes that sorted between color morphs during seed development. Crosses between dark pollen plants from different subspecies showed signs of complementation in the F2 generation, but the frequency of the light morph was too low to support a model involving complementary action of recessive alleles at two separate loci. Based on this and other observations, we hypothesize that the pollen color difference is controlled by the same major locus in the two subspecies.     

Evolutionary maintenance of stigma-height dimorphism in Narcissus papyraceus (Amaryllidaceae)

Stigma-height dimorphism is a sexual polymorphism in which plant populations are composed of two floral morphs that differ significantly in style length but not anther position. The morphs exhibit approach and reverse herkogamy, floral designs that in most species typically occur as monomorphic conditions. We investigated the floral biology of stigma-height dimorphism in the Mediterranean geophyte Narcissus papyraceus (Amaryllidaceae) in an effort to understand the evolutionary forces maintaining stylar polymorphism. Our survey of 66 populations in Spain, Portugal, and Morocco indicated that 56% were dimorphic with the long-styled morph at an average frequency of 0.79. The remaining 44% of populations sampled were monomorphic for the long-styled morph. In dimorphic populations there was a significant positive relation between population size and the frequency of the short-styled morph. Controlled pollinations demonstrated that N. papyraceus is self-sterile with no significant differences in female fertility between intra- and intermorph crosses. Prior self-pollination reduced seed set in flowers that were subsequently cross-pollinated. Estimates of mating patterns using allozyme markers in eight populations indicated that N. papyraceus is largely outcrossing (mean t(m) = 0.81) with no significant differences between monomorphic and dimorphic populations or style morphs. Stigma-height dimorphism in N. papyraceus is maintained in populations by insect-mediated cross-pollination with biased morph ratios and stylar monomorphism likely resulting from the combined influence of the inheritance of the polymorphism, morph-specific differences in assortative mating and founder effects.     

Janusia anisandra (A. Juss.) Griseb (Malpighiaceae): The first case of enantiostyly in oil-flower species

Enantiostyly is a floral polymorphism characterized by style deflection to the right and left, which results in flowers with mirror images. To date, enantiostyly occurs only in species that offer pollen or nectar as floral resource. Here we describe the first case of enantiostyly in an oil-flower species. Janusia anisandra (A. Juss.) Griseb (Malpighiaceae) shows right and left-styled flowers in individuals occurring in an area of tropical dry forest in Northeastern Brazil. We described the floral morphology, investigate the reproductive system, and made focal observations of flower visitors behaviour. J. anisandra has morphological traits that are part of the floral conservatism found in the neotropical species of Malpighiaceae, which preserves features that are decisive for the interaction with oil-collecting bees of the Centridini tribe, performing a highly specialized pollination system. The six stamens (two major and four smaller), located in the center of the flower, characterizes heteranthery, an intrafloral polymorphism, in which the stamens differ in shape, size, and function and is commonly associated with enantiostyly. We identified the two floral morphs in the same individual, characterizing a monomorphic enantiostyly; each of the morphs differs by lateral displacement of the style to the right or to the left, always accompanied by one larger stamen. The species is moderately self-compatible. Four species of solitary bees of the genus Centris were registered visiting the two morphs of J. anisandra flowers. Centris aenea and C. fuscata were the main pollinators, performing 65% of the visits. This new discovery of a classical monomorphic enantiostyly in J. anisandra opens the way for investigations in the evolution of this system in oil-secreting flowers.     

The intriguing complexity of parthenogenesis inheritance in Pilosella rubra (Asteraceae, Lactuceae)

Neither the genetic basis nor the inheritance of apomixis is fully understood in plants. The present study is focused on the inheritance of parthenogenesis, one of the basic elements of apomixis, in Pilosella (Asteraceae). A complex pattern of inheritance was recorded in the segregating F(1) progeny recovered from reciprocal crosses between the facultatively apomictic hexaploid P. rubra and the sexual tetraploid P. officinarum. Although both female and male reduced gametes of P. rubra transmitted parthenogenesis at the same rate in the reciprocal crosses, the resulting segregating F(1) progeny inherited parthenogenesis at different rates. The actual transmission rates of parthenogenesis were significantly correlated with the mode of origin of the respective F(1) progeny class. The inheritance of parthenogenesis was significantly reduced in F(1) n?+?n hybrid progeny from the cross where parthenogenesis was transmitted by female gametes. In F(1) n?+?0 polyhaploid progeny from the same cross, however, the transmission rate of parthenogenesis was high; all fertile polyhaploids were parthenogenetic. It appeared that reduced female gametes transmitting parthenogenesis preferentially developed parthenogenetically and only rarely were fertilized in P. rubra. The fact that the determinant for parthenogenesis acts gametophytically in Pilosella and the precocious embryogenesis in parthenogenesis-transmitting megagametophytes was suggested as the most probable explanations for this observation. Furthermore, we observed the different expression of complete apomixis in the non-segregating F(1) 2n?+?n hybrids as compared to their apomictic maternal parent P. rubra. We suggest that this difference is a result of unspecified interactions between the parental genomes.     

Inheritance of glabrous plants in <Emphasis Type="Italic">Helianthemum oelandicum</Emphasis> var. <Emphasis Type="Italic">oelandicum</Emphasis> and spatial patterns of allele frequencies in local populations

Helianthemum oelandicum var. oelandicum is an endemic taxon on the Baltic island of Öland, SE Sweden. Plants can be classified into two morphs: the bristled morph (with bristles and with or without scattered stellate hairs) and the glabrous morph (without bristles and stellate hairs). In crosses between plants assumed to be homozygous for the trait that characterises the phenotypes of the two morphs, offspring in F1 could not be distinguished from the bristled morph. Segregation in F2 did not deviate from the expected 3:1 ratio (bristled morphs/glabrous morphs), indicating one major gene with a dominant allele for the phenotype of the bristled morph and a recessive allele for the phenotype of the glabrous morph. Besides the Mendelian inheritance of presence/absence of hairs, the density of hairs appeared to be further modified by quantitative genes. The frequency of the recessive allele for the phenotype of the glabrous morph varied among local populations and showed a geographical structure, both on local and regional scales. Possible mechanisms behind the spatial variation in indumentum are discussed.     

Inheritance of resistance to clopyralid and picloram in yellow starthistle (Centaurea solstitialis L.) is controlled by a single nuclear recessive gene

The noxious weed yellow starthistle (Centaurea solstitialis L.) can be controlled effectively at the seedling stage with foliar application of the auxinic herbicides picloram or clopyralid. Although resistance to these herbicides is rare, a yellow starthistle biotype resistant to picloram and cross-resistant to clopyralid was observed in 1989 near Dayton, WA, in a pasture that had been subjected to intensive picloram selective pressure. Our objective was to determine the mode of inheritance for this resistance trait. Transmission of the resistant phenotype was monitored in reciprocal F(1) crosses between susceptible (SCI) and resistant (RDW) plants, their testcross and pseudo-F(2) progeny. Progeny from all crosses, as well as RDW and SCI seedlings of original populations, were sprayed with picloram or clopyralid to distinguish between susceptible and resistant individuals. All F(1) progeny were susceptible to both herbicides, indicating that the resistance trait was of nuclear origin and recessive in nature. Segregation of the resistant phenotype among pseudo-F(2) and testcross progeny of F(1) genotypes demonstrated monofactorial inheritance (P >.25) for resistance to both herbicides. The conclusion that resistance is conferred by a single recessive allele is consistent with the observation that no other picloram-resistant yellow starthistle populations have been identified in the area since picloram selection pressure was abated.     

Sex-linked expression of a sexually selected trait in the stalk-eyed fly, Cyrtodiopsis dalmanni

Recent theoretical and empirical work has suggested that the X chromosome may play a special role in the evolution of sexually dimorphic traits. We tested this idea by quantifying sex chromosome influence on male relative eyespan, a dramatically sexually selected trait in the stalk-eyed fly, Cyrtodiopsis dalmanni. After 31 generations of artificial sexual selection on eyespan:body length ratio, we reciprocally crossed high- with low-line flies and found no evidence for maternal effects; the relative eyespan of F1 females from high- and low-line dams did not differ. However, F1 male progeny from high-line dams had longer relative eyespan than male progeny from low-line dams, indicating X-linkage. Comparison of progeny from a backcross involving reciprocal F1 males and control line females confirmed X-linked inheritance and indicated no effect of the Y chromosome on relative eyespan. We estimated that the X chromosome accounts for 25% (SE = 6%) of the change in selected lines, using the average difference between reciprocal F1 males divided by the difference between parental males, or 34%, using estimates of the number of effective factors obtained from reciprocal crosses between a high and low line. These estimates exceed the relative size of the X in the diploid genome of a male, 11.9% (SE = 0.3%), as measured from mitotic chromosome lengths. However, they match expectations if X-linked genes in males exhibit dosage compensation by twofold hyperactivation, as has been observed in other flies. Therefore, sex-linked expression of relative eyespan is likely to be commensurate with the size of the X chromosome in this dramatically dimorphic species.     

Sexual reproduction, hybridization, apomixis, and polyploidization in the genus Boechera (Brassicaceae)

Of the 340 genera in the Brassicaceae, apomictic reproduction is found only in the North American genus Boechera. We investigated phylogenetic relationships, ability to hybridize, mating system, and ploidy levels of 92 lines sampled from 85 populations and representing 19 Boechera species. Phylogenetic analyses based on chloroplast DNA sequences identified three lineages in the genus. Reciprocal crosses of each line were made to a common sexual diploid B. stricta tester. The resulting F(1) progeny were analyzed for the inheritance of polymorphic microsatellite loci, genome size, and seed production. Intraspecific B. stricta crosses confirmed that this species is mostly diploid and sexual. Interspecific crosses revealed many other species were diploid and sexual and could be successfully hybridized with the tester. We also found obligate and facultative apomictic diploid and triploid lines. De novo F(1) polyploids (either triploids or tetraploids) were derived from the union of nonreduced (from an apomictic parent) and reduced (from the tester) gametes. However, seed production of these F(1) plants was generally low, suggesting a failure in the transmission of apomixis. The creation of a wide array of segregating genetic populations will facilitate future research on the evolution and inheritance of quantitative variation in Boechera.     

Enantiostyly in Chamaecrista ramosa (Fabaceae‐Caesalpinioideae): floral morphology,pollen transfer dynamics and breeding system

Enantiostyly is a form of reciprocal herkogamy, in which floral morphs present reciprocal differences in the position of sexual elements, and occurs in monomorphic and dimorphic forms. This polymorphism maximises cross‐pollination and reduces self‐pollination, being very common within the subtribe Cassiinae (Fabaceae). Nevertheless, few studies have investigated the functionality of enantiostyly, particularly in this plant group. The present study aimed to investigate enantiostyly and its functionality in Chamaecrista ramosa, a monomorphic enantiostylous shrub, in an area of coastal vegetation in northeast Brazil. Pollen deposition and capture on the body of floral visitors, the relationship of these data with floral biology and breeding system, and morph ratio were evaluated. Pollen deposition and capture occurred in specific sites of the floral visitor body, showing the functionality of enantiostyly. The floral architecture, associated with the floral visitor behaviour, resulted in indirect pollen deposition on the floral visitor body. This occurred through a loop made by the pollen upon the inner petal surface, similar that generally reported for other Cassiinae. Chamaecrista ramosa is self‐compatible, although no fruit set was observed through spontaneous self‐pollination. The occurrence and number of floral morphs was similar within clumps. Enantiostyly seems to be advantageous for this species, as it results in efficient pollen capture and deposition, reduces the chances of autogamy and maximises intermorph pollen flow.     

A theoretical investigation of the evolution and maintenance of mirror-image flowers

Enantiostyly is the deflection of the female sex organ either to the left or to the right side of the floral axis, resulting in mirror-image flowers. Two types of enantiostyly occur: in monomorphic enantiostyly, individuals exhibit both flower forms, whereas in dimorphic enantiostyly, the forms occur on separate plants. Monomorphic enantiostyly is known from at least 10 families, whereas dimorphic enantiostyly is reported in only three. Phylogenetic evidence suggests that monomorphic enantiostyly has evolved from a straight-styled ancestor and that dimorphic enantiostyly is derived from monomorphic enantiostyly. Here, we use theoretical models to investigate the role of pollen transfer in influencing these evolutionary transitions. We used numerical calculations to examine the evolution of monomorphic and dimorphic enantiostyly under different conditions of pollen transfer, inbreeding depression, and pollinator visitation. Our results demonstrate that in comparison to a putative straight-styled ancestor, both monomorphic and dimorphic enantiostyly function to reduce geitonogamous pollen transfer with a concomitant increase in pollen export. Our calculations suggest that the first stage in the evolution of monomorphic enantiostyly involves the deflection of the style only, followed by selection for reciprocity in anther position to promote more precise cross-pollination. Constraints associated with the developmental genetics of left-right asymmetries may account for the low number of evolutionary transitions from monomorphic to dimorphic enantiostyly, despite the evolutionary stability of this condition once it arises.     

Mating patterns and demography in the tristylous daffodil Narcissus triandrus

Mating patterns in plant populations are influenced by interactions between reproductive traits and ecological conditions, both factors that are likely to vary geographically. Narcissus triandrus, a wide-ranging heterostylous herb, exhibits populations with either two (dimorphic) or three (trimorphic) style morphs and displays substantial geographical variation in demographic attributes and floral morphology. Here, we investigate this variation to determine if demography, morphology, and mating system differ between the two sexual systems. Our surveys in Portugal and NW Spain indicated that dimorphic populations were less dense, of smaller size, and had larger plants and flowers compared to trimorphic populations. Outcrossing rates estimated using allozyme markers revealed similar outcrossing rates in dimorphic and trimorphic populations (t(m) dimorphic=0.759; t(m) trimorphic=0.710). All populations experienced significant inbreeding in progeny (mean F=0.143). In contrast, parental estimates of inbreeding were not significantly different from zero (mean F=0.062), implying that few inbred offspring survive to reproductive maturity due to inbreeding depression. Although the majority of inbreeding results from selfing, significant levels of biparental inbreeding were also detected in eight of the nine populations (mean s(s)-s(m)=0.081). Density was negatively associated with levels of selfing but positively associated with biparental inbreeding. Population size was positively associated with outcrossing but not biparental inbreeding. There were no consistent differences among the style morphs in outcrossing or biparental inbreeding indicating that the maintenance of trimorphism vs dimorphism is unlikely to be associated with inbreeding of maternal parents.     

Experimental tests of the function of mirror-image flowers

Enantiostyly, the reciprocal deflection of the style to the left or right side of the floral axis has evolved independently in at least a dozen angiosperm families. Unlike other plant sexual polymorphisms, the adaptive significance of these mirror‐image flowers remains unclear. Most authors have interpreted enantiostyly as a floral mechanism that promotes cross‐pollination. However, any functional interpretation is complicated by the fact that enantiostyly occurs in two forms. In monomorphic enantiostyly there are left‐ and right‐styled flowers on the same plant, while in dimorphic enantiostyly they are on separate individuals. In this paper we develop a model of pollen transfer which indicates that monomorphic enantiostyly should reduce geitonogamous pollination compared to a non‐enantiostylous condition, and that the lowest levels of geitonogamous pollination should occur in dimorphic enantiostyly. We tested these predictions using floral manipulations of bee‐pollinated Solanum rostratum in garden arrays. We compared mating patterns and fertility in five array types: non‐enantiostylous and straight‐styled, monomorphic enantiostylous, dimorphic enantiostylous, and arrays uniform for either left or right stylar deflection. Outcrossing rates in non‐enantiostylous arrays (t = 0.33 ± 0.04) were significantly lower than all other arrays, while monomorphic enantiostylous arrays (t = 0.74 ± 0.06) had significantly lower outcrossing rates than dimorphic enantiostylous arrays (t = 0.88 ± 0.04) and those uniform for stylar deflection (t = 0.84 ± 0.04). In dimorphic enantiostylous arrays, intermorph pollen transfer accounted for 75% of all outcrossing events. In pollen‐limited situations, both types of enantiostylous arrays had significantly higher female fertility than arrays fixed for one direction, demonstrating that enantiostyly promotes pollen transfer between flowers of opposite stylar orientation. Our results provide support for the hypothesis that enantiostyly functions to increase the precision of cross‐pollination in bee‐pollinated plants by reducing geitonogamy. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 85 , 167–179.     

Inheritance of a hair character in <Emphasis Type="Italic">Helianthemum oelandicum</Emphasis> var. <Emphasis Type="Italic">canescens</Emphasis> and allele frequencies in natural populations

Helianthemum oelandicum var. canescens (Hartm.) Fr. is an endemic taxon with a restricted distribution (less than 10 km²) in the southernmost part of the Baltic island of Öland, SE, Sweden. The taxon varies with respect to stellate hairs. Most plants can be classified into two morphs, the stellated morph (with a dense carpet of stellate hairs on the abaxial surface of the leaves) and the bristled morph (without a carpet of stellate hairs). In crosses between plants assumed to be homozygous for the trait that characterises the phenotypes of the two morphs, F1 offspring was indistinguishable from the bristled morph. Segregation in F2 did not deviate from the expected 3:1 ratio (bristled morph/stellated morph), indicating one major gene with a dominant allele for the phenotype of the bristled morph and a recessive allele for the phenotype of the stellated morph. Besides the Mendelian inheritance of the presence/absence of a whitish cover of stellate hairs, the density of hairs appeared to be further modified by quantitative genes. The frequency of the recessive allele for the phenotype of the stellated morph varied among populations and showed a geographical structure. Possible mechanisms behind the spatial variation in indumentum are discussed.     

The Genetic Basis of Sex Ratio in Silene Alba (= S. Latifolia)

A survey of maternal families collected from natural populations showed that the sex ratio in Silene alba was slightly female biased. Sex ratio varied among populations and among families within a female biased population. Crosses among plants from the most female biased population and the most male biased population showed that the sex ratio polymorphism was inherited through or expressed in the male parent. Males from one family in particular exhibited a severe female bias, characterized by less than 20% male progeny. The inheritance of sex ratio was investigated using a reciprocal crossing design. Sex ratios from reciprocal crosses were significantly different, indicating either sex-linkage or cytoplasmic inheritance of sex ratio. The sex ratios produced by males generally resembled the sex ratios produced by their male parents, indicating that the sex ratio modifier was Y linked. The maternal parent also significantly influenced sex ratio through an interaction with the genotype of the paternal parent. Sex ratio, therefore, is apparently controlled by several loci. Although sex ratio bias in this species may be due to deleterious alleles on the Y chromosome, it is more likely to involve an interaction between loci that cause the female bias and a Y-linked locus that enhances the proportion of males in the progeny.     

Genetic basis of tristyly in tetraploid Oxalis alpina (Oxalidaceae)

The inheritance of style‐morphs was investigated in tetraploid populations of tristylous Oxalis alpina (Oxalidaceae) to determine if alleles controlling style‐morphs are expressed at duplicated loci. In tetraploid populations, a dominant S allele leads to expression of the short‐styled phenotype at the short/non‐short locus and is epistatic to the M allele at the mid/long locus. The M allele results in expression of the mid‐styled phenotype but only if the S allele is absent. Long‐styled morphs are homozygous recessive at the short and mid loci. Test crosses of many tetraploid short‐styled individuals resulted in segregations of short‐, mid‐ and long‐styled individuals which, because of linkage between the short and mid loci, can only occur with polyploidy and expression of alleles at duplicated loci. Segregation patterns from three crosses suggest the possibility of disomic inheritance via preferential pairing of chromosomes in tetraploid populations of O. alpina. Segregation patterns in the progeny of mid‐styled individuals indicated that only a few individuals had more than one copy of the M allele, despite the potential for accumulation of M alleles via self‐fertilization of partially self‐compatible mid‐styled morphs in some populations. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 179 , 308–318.