Plasticity of reproductive components at different stages of development in the annual plant Thlaspi arvense L.

Summary This study examines the effect of different densities and the removal of all neighbours at different stages of development on all components of reproduction in the inbreeding annual Thlaspi arvense L. A 64-fold increase in density significantly reduced all repooductive components. The number of flower buds per plant was decreased most strongly; the order of decreasing plasticity among the other components was number of capsules per flower, individual seed weight, ovule number per capsule, flowers per flower bud and seeds per ovule. Removing neighbours at all stages of development increased seed yield of plants in comparison to the control without density reduction, but patterns of plasticity depended strongly on time of treatment. The main effect of the removal of neighbours at the vegetative stage was to increase the number of flowers per plant, but the number of ovules per capsule and seed weight increased also, and abortion of capsules decreased. Removing neighbours at the onset of flowering initially failed to affect flower number per plant, instead it resulted in a strong reduction of capsule abortion and an increase in seed weight. However, several weeks after flowering had initially ceased, fresh lateral inflorescences were produced, resulting in a second flush of reproduction. Removing neighbours at the stage of fruit ripening resulted at first only in an increase in seed witht, but later a second reproductive phase occurred. Fresh lateral branches were produced, but the apical meristem was also reactivated. The overall pattern of plasticity among all reproductive components in response to a removal of neighbours was the same as in response to density. The position of a capsule along the inflorescence influenced its number of ovules, the rate of seed abortion and the mean weight of seeds, with the type of effect depending on the developmental stage at which neighbours were removed. Significant negative correlations were found between the mean weight of seeds and the number of seeds in a capsule under all treatments.     

Ovule number per flower in a world of unpredictable pollination

The number of ovules per flower varies over several orders of magnitude among angiosperms. Here we consider evidence that stochastic uncertainty in pollen receipt and ovule fertilization has been a selective factor in the evolution of ovule number per flower. We hypothesize that stochastic variation in floral mating success creates an advantage to producing many ovules per flower because a plant will often gain more fitness from occasional abundant seed production in randomly successful flowers than it loses in resource commitment to less successful flowers. Greater statistical dispersion in pollination and fertilization among flowers increases the frequency of windfall success, which should increase the strength of selection for greater ovule number per flower. We therefore looked for evidence of a positive relationship between ovule number per flower and the statistical dispersion of pollen receipt or seed number per flower in a comparative analysis involving 187 angiosperm species. We found strong evidence of such a relationship. Our results support the hypothesis that unpredictable variation in mating success at the floral level has been a factor in the evolution of ovule packaging in angiosperms.     

Structural aspects of ovule and seed development and nonrandom abortion inMelilotus officinalis (Fabaceae)

Summary Only one ovule matures into a seed inMelilotus officinalis. Although eight ovules form within an ovary, only the basal ovule develops into a mature seed, whereas the other ovules degenerate. The investigation of ovule and seed structure at different developmental stages and a comparison of quantitative characters of differently fated ovules within an ovary were undertaken by light, phase contrast, and fluorescence microscopy. In this species, campylotropous ovules develop simultaneously on marginal placentae in an apocarpous unilocular gynoecium. Megasporo- and megagametogenesis proceed normally and are completed in bud. The maturation of the Polygonum type embryo sac takes place after the flower opens. Shortly before fertilization, synergids show signs of degeneration in all ovules. At this stage, neither the structure nor the sizes of ovules within one ovary differ significantly. In spite of this, only the basal ovule develops into a seed. Rarely, one of the upper-situated ovules or the basal and another ovule mature into seeds. Seed enlargement is insignificant until the stage when globular embryo and nuclear endosperm are formed. At the seed-filling stage, other ovules have collapsed and the seed gradually comes to occupy the total volume of the pod. The fruit-to-seed length ratio decreases considerably during seed ripening. At fertilization, ovary length is four times greater than ovule length. In the mature state, the fruit and seed lengths are approximately equal. Seed size and weight diminish with an increase in seed number within a pod, although pod size remains constant. It is assumed that nonrandom abortion of young seeds inM. officinalis is under maternal control and is not related to structural abnormalities in ovule development or with limitation in pollen. We suppose that evolution of this species may have proceeded in the direction of a decrease in seed number and an increase in its sizes, which may play an important role in seed dispersal and seedling establishment.     

Variation in ovule and seed size and associated size-number trade-offs in angiosperms

Unlike pollen and seed size, the extent and causes of variation in ovule size remain unexplored. Based on 45 angiosperm species, we assessed whether intra- and interspecific variation in ovule size is consistent with cost minimization during ovule production or allows maternal plants to dominate conflict with their seeds concerning resource investment. Despite considerable intraspecific variation in ovule volume (mean CV = 0.356), ovule production by few species was subject to a size-number trade-off. Among the sampled species, ovule volume varied two orders of magnitude, whereas seed volume varied four orders of magnitude. Ovule volume varied positively among species with flower mass and negatively with ovule number. Tenuinucellate ovules were generally larger that crassinucellate ovules, and species with apical placentation (which mostly have uniovulate ovaries) had smaller ovules than those with other placentation types. Seed volume varied positively among species with fruit mass and seed development time, but negatively with seed number. Seeds grew a median 93-fold larger than the ovules from which they originated. Our results provide equivocal evidence that selection minimizes ovule size to allow efficient resource allocation after fertilization, but stronger evidence that ovule size affords maternal plants an advantage in parent-offspring conflict.     

Control of fecundity through abortion in Epilobium montanum L.

Summary Plants of the inbreeding perennial herb Epilobium montanum L. were defoliated at two stages in development and the formation and abortion of flower buds, flowers, copsules and ovules was compared with control plants. A comparison was also made of the effects of self- and cross-pollination on fecundily. Defoliation reduced the number of flower buds formed but its greatest effect was to increase the abortion of flower buds. Defoliation also caused earlier abortions which were generally lower on the racemes of the treated than on the control plants. The abortion of flowers and capsules was much less significant. The number of ovules formed per capsule decreased with height on the raceme and the abortion rate of ovules was increased by defoliation. The pattern of ovule abortion within the capsules differed between cross- and self-pollinated plants but the number of seeds ripened was not affected. The overall survivorship of ovules to mature seeds was 89.3% which compares with the average of 85% found by Wiens for inbreeding annuals. The findings suggest that such high values of ovule survivorship may be characteristics of normally inbreeding species irrespective of whether they are annuals or perennials.     

VARIATION AND COVARIATION AMONG FLORAL TRAITS WITHIN AND AMONG FOUR SPECIES OF NORTHERN EUROPEAN PRIMULA (PRIMULACEAE)

Phenotypic and genetic variation and correlations among floral traits within and among four Primula species were measured to seek evidence for potential constraints on the independent evolution of floral characters, to examine the relationship between mating system, ploidy level, and sex allocation, and to determine whether some traits are more conservative than others within and across these congeners. We measured mean flower diameter, corolla depth, pollen production, modal pollen grain volume, ovule number per flower, and pollen: ovule ratios for 64 field-collected genotypes from northern Europe. These represented one heterostylous (P. farinosa: 2n = 18) and three homostylous (P. scotica: 2n = 54, P. scahdinavica: 2n = 74, and P. stricta: 2n ~ 126) species. All traits differed significantly among species and among the six taxon/morph categories identified (including three morphs of P. farinosa: pin, thrum, and homostylous). Pollen production per flower was significantly higher (and individual pollen grain volume lower) in the outcrossing P. farinosa than in any of the homostylous species; also, pin morphs produced significantly more pollen per flower than thrums in P. farinosa. Among the homostylous species, there were significant differences in all traits except modal pollen grain volume. Ovule number per flower and flower size were less variable among taxa than pollen production and pollen volume. Within species, there were several strong negative correlations among genets between pairs of traits, but each species exhibited a unique set of inverse relationships. We detected only one significant positive genetic correlation; in P. stricta, ovule number and pollen production per flower were positively correlated among genets. Among species means, two pairs of traits were negatively correlated: mean ovule number per flower vs. flower diameter (but P = 0.0587), and mean pollen production per flower vs. modal pollen grain volume. These negative correlations within and among taxa suggest that there may be intrinsic genetic constraints on the independent evolution of these floral characters, but that these constraints differ among species.     

Pollen-limited seed set in pseudogamous blackberries (Rubus L. subgen. Rubus)

Summary Pseudogamous blackberry species are polyploid and usually exhibit meiotic irregularities causing severe reduction in pollen viability. When species means were compared, relative seed set was strongly correlated with the number of good pollen grains produced per flower divided by the number of ovules (good-pollen/ovule ratio).Partial correlation analysis for percentage viable pollen and relative seed set, controlling for good-pollen/ovule ratio, revealed an almost significant relationship, presumably because meiotic irregularities have a similar effect on both pollen viability and the viability of meiotically derived embryo sacs. Seed germination, on the other hand, showed no relationship with relative seed set or with pollen viability.The automatic selfing capacity exhibited by most of these blackberry species does not appear to be related to either pollen production or relative seed set.     

Competition and the compensatory regulation of fruit and seed set in the perennial herb Epilobium dodonaei (Onagraceae)

I studied the effects of competition and soil fertilization on variation of seed yield components of the outcrossing perennial Epilobium dodonaei Vill. using a randomized complete block design. Fertilization as a main effect was not significant. Competition, however, reduced the number of flower buds per shoot (-29%), the number of ovules per fruit (-12%), and the number of ripe fruits per shoot (-51%). In addition, competition caused an increase in abortion of flower buds. Consequently the fruit/flower bud ratio decreased from 0.71 to 0.47. Average seed mass was not reduced significantly by competition. Some of the negative effects of competition on fruit production were mitigated by fertilization. However, competition considerably reduced the proportion of late-aborted seeds, which resulted in an increase of the seed/ovule ratio from 0.31 to 0.49 (+58%). As a consequence of this compensation, the reduction in the number of seeds per shoot due to competition was not significant. At the level of the genet, competition had a strong effect on seed yield due to decreases in the number of shoots produced. I discuss patterns of regulation at consecutive levels of reproduction. Shoots of plants suffering from competition initially invested less in reproductive structures than the control and showed a higher abortion rate of less costly structures early in reproductive development, but also had a lower abortion rate later in their development. The observed compensatory pattern in yield components illustrates the fine-tuning regulation capacity at different levels of reproductive development in plants.     

Solitary plants do as well as clumped ones in Silene uniflora (Caryophyllaceae)

Many studies have been done on seed production as a function of population density in wild plants Most of them show a higher seed-set per flower of densely growing plants In this study, in a gynodioecious Silene uniflora (Caryophyllaceae) population on the Baltic island of Oland, high plant density did not increase fruit-set or seed-set Instead, the total number of seeds set was slightly higher for widely scattered plants as a result of a somewhat lower number of ovules per flower in densely growing plants Individuals had nothing to gain by growing close together, because there was no reproductive parameter which could compensate for the low ovule number per flower of closely growing plants Plant size determined the total seed production of individuals, but did not correlate with any of the fitness components studied per flower basis The different gender morphs showed the same pattern, which is discussed as a comparison with pollen limitation in self-incompatible and self-incompatible plants     

Reproductive effort in desert versus mediterranean crucifers: the allogamous Erucaria rostrata and E. hispanica and the autogamous Erophila minima

Components of the total sexual investment of plants growing under mediterranean climatic and edaphic conditions were compared with those of plants growing in the desert, in the closely related allogamous species pair Erucaria hispanica and E. rostrata and in populations of the autogamous species Erophila minima. In all cases lower total investment was evident in the desert plants. At the prezygotic phase it was expressed by (1) reduced production of flowers; (2) lower allocation to the production of male gametophytes and some floral organs; and (3) packaging of more ovules per ovary. The ratio of reproductive: vegetative biomass which was found to be greater in the desert plants and their lower pollen: ovule ratio are perhaps indicative of greater efficiency. Their smaller investment at the postzygotic phase was expressed in: (1) reduction in total numbers of fruits and seeds; (2) decrease in seed size and weight. Yet in the desert plants the number of seeds per total biomass was found to be significantly larger and fertility rates (seed-set per ovule, fruit-set per flower per plant) were equal to or greater than those in the mediterranean plants. The trends observed in this study in desert plants, which may result in more efficient exploitation of resources, are similar in the species involved, regardless of their breeding system-autogamous or allogamous.     

The evolution of ovule number and flower size in wind-pollinated plants

In angiosperms, ovules are "packaged" within individual flowers, and an optimal strategy should occur depending on pollination and resource conditions. In animal-pollinated species, wide variation in ovule number per flower occurs, and this contrasts with wind-pollinated plants, where most species possess uniovulate flowers. This pattern is usually explained as an adaptive response to low pollen receipt in wind-pollinated species. Here, we develop a phenotypic model for the evolution of ovule number per flower that incorporates the aerodynamics of pollen capture and a fixed resource pool for provisioning of flowers, ovules, and seeds. Our results challenge the prevailing explanation for the association between uniovulate flowers and wind pollination. We demonstrate that when flowers are small and inexpensive, as they are in wind-pollinated species, ovule number should be minimized and lower than the average number of pollen tubes per style, even under stochastic pollination and fertilization regimes. The model predicts that plants benefit from producing many small inexpensive flowers, even though some flowers capture too few pollen grains to fertilize their ovules. Wind-pollinated plants with numerous flowers distributed throughout the inflorescence, each with a single ovule or a few ovules, sample more of the airstream, and this should maximize pollen capture and seed production.     

EFFECT OF OVULE POSITION ON SEED PRODUCTION,SEED WEIGHT,AND PROGENY PERFORMANCE IN PHASEOLUS COCCINEUS L. (LEGUMINOSAE)

We examined the effect of ovule position within the ovary on the probability of seed maturation, on seed weight, and on progeny performance in the outbreeding legume Phaseolus coccineus. Ovaries of P. coccineus possess six linearly arranged ovules (ovule position one = stylar end). We found that in both 1987 and 1988, ovule position had a significant effect on the probability of seed maturation under field conditions. In 1987, ovule positions one. two, and three had a higher probability of maturing seeds than the three most basal ovule positions. In 1988, the probability of producing a mature seed in ovule position one was more similar to the three most basal ovule positions than to ovule positions two and three. The position of the ovule in the ovary had no significant effect on seed weight in 1987, but it had a significant effect in 1988. Overall, seeds from ovule positions one, two, and three tended to produce heavier seeds than the three most basal ovule positions. The effects of ovule position on progeny performance were determined in a greenhouse and a field study. In the greenhouse study, we found no significant overall effect of the position of the ovule that produced the seed on progeny performance. In the field study, we did find a significant ovule position effect on several measures of reproductive performance as well as an overall effect on reproductive performance. In addition, we found a significant interaction between ovule position and number of seeds per fruit. Progeny from the stylar end of the fruit outperformed the progeny from the peduncular end in fruits containing many seeds, whereas there were no significant differences between progeny produced in the stylar and peduncular ends of fruits containing few seeds. Causes of position effects are unknown but hypotheses abound.     

Within-carpel and among-carpel competition during seed development, and selection on carpel number, in the apocarpous perennial herb Helleborus foetidus L. (Ranunculaceae)

Apocarpous flowers share opportunities for post-fertilization ovule selection among more functional levels than syncarpous flowers, because the occurrence of a variable number of unfused carpels adds a new source of variation to the likelihood of successful female reproduction. The extent to which post-fertilization events might differ among these unfused carpels may promote variations in the reproductive strategies of plants. We report a study of the variation, within and among carpels and flowers, in seed production and mass in the apocarpous Helleborus foetidus (Ranunculaceae), in relation to the number of carpels per flower. Differences within and among carpels in female reproductive success were affected by carpel number and pollination environment. When analysing whole flowers as functional units we also found that the magnitude of the differences related to carpel number and pollination treatment actually depended on the “distribution” of pollen types within flowers. Thus, variable within-flower pollination environments, more likely to occur in apocarpous than in syncarpous flowers, may affect the strategies of resource allocation for fruit development at different stages of the reproductive process. Regarding seed production, we found that producing more flowers with four carpels was under directional; however, when mean diaspore mass was considered as a measure of fitness, directional selection was found on producing flowers with two and three carpels (the modal carpel number found in wild populations). We discuss ecological and developmental reasons which could explain the observed pattern, and conclude that selection on an optimum carpel number may be very variable across the species range, as the discussed reasons may impose constraints on eventual evolutionary response, thus contributing to the maintenance of the intra-individual variability in carpel number.     

MEASUREMENTS OF NATURAL SELECTION ON FLORAL TRAITS IN WILD RADISH (RAPHANUS RAPHANISTRUM). I. SELECTION THROUGH LIFETIME FEMALE FITNESS

Although the role of natural selection in the evolution of floral traits has been of great interest to biologists since Darwin, studies of selection on floral traits through differences in lifetime fitness have been rare. We measured selection acting on flower number, flower size, stigma exsertion, and ovule number per flower using field data on lifetime female fitness (seed production) in wild radish, Raphanus raphanistrum. The patterns of selection were reasonably consistent across three field seasons, with strong directional selection for increased flower production in all three years, weaker selection for increased ovule number per flower in two years, and selection for increased flower size in one year. The causes of the selection were investigated using path analysis combined with multiplicative fitness components. Increased flower production increased fruit production directly, and increased numbers of ovules per flower increased the number of seeds per fruit in all three years; pollinator visitation did not influence either of these fitness components. Increased flower size was associated with increases in both the number of fruit and the number of seeds per fruit in one year, with the latter relationship being stronger. Total lifetime seed production was affected more strongly by differences in fruit production than by differences in either the number of seeds per fruit or the proportion of fertilized seeds that were viable, but all three fitness components were positively correlated with total seed production.     

Sources of variation in pollinator contribution within a guild: the effects of plant and pollinator factors

Among plants visited by many pollinator species, the relative contribution of each pollinator to plant reproduction is determined by variation in both pollinator and plant traits. Here we evaluate how pollinator movement among plants, apparent pollen carryover, ovule number, resource limitation of seed set, and pollen output affect variation in contribution of individual pollinator species to seed set in Lithophragma parviflorum (Saxifragaceae), a species visited by a broad spectrum of visitors, including beeflies, bees and a moth species. A previous study demonstrated differences among visitor species in their single-visit pollination efficacy but did not evaluate how differences in visitation patterns and pollen carryover affect pollinator efficacy. Incorporation of differential visitation patterns and pollen carryover effects —commonly cited as potentially important in evaluating pollinator guilds — had minor effects (0–0.6% change) on the estimates of relative contribution based on visit frequency and single-visit efficacy alone. Beeflies visited significantly more flowers per inflorescence than the bees and the moth. Seed set remained virtually constant during the first three visited flowers for beeflies and larger bees, indicating that apparent pollen carryover did not reduce per-visit efficacy of these taxa. In contrast, Greya moth visits showed a decrease in seed set by 55.4% and the smaller bees by 45.4% from first to second flower. The larger carryover effects in smaller bees and Greya were diminished in importance by their small overall contribution to seed set. Three variable plant traits may affect seed set: ovule number, resource limitation on seed maturation, and pollen output. Ovule number per flower declined strongly with later position within inflorescences. Numbers were much higher in first-year greenhouse-grown plants than in field populations, and differences increased during 3 years of study. Mean pollen count by position varied 7-fold among flowers; it paralleled ovule number variation, resulting in a relatively stable pollen:ovule ratio. Resource limitation of seed set increased strongly with later flowering, with seed set in hand-pollinated flowers ranging from 66% in early flowers to 0% in the last two flowers of all plants. Variation in ovule number and resource limitation of seed maturation jointly had a strong effect on the number of seeds per flower. Visitation to early flowers had the potential to cause more seed set than visitation to later flowers. Overall, the most important sources of variation to seed production contribution were differences among pollinators in abundance and absolute efficacy (ovules fertilized on a single visit) and potentially differential phenology among visitor species. These effects are likely to vary among populations and years.     

Effects of floral sexual investment and dichogamy on floral longevity

Aims Floral longevity, the duration that a flower remains open and functional, varies greatly among species. Variation in floral longevity has been considered to be optimal strategy for resource allocation under different ecological conditions, mainly determined by the rates of pollination and cost of flower maintenance. However, it is unclear whether an intrinsic factor, floral sexual investment, constrains evolution of floral longevity. The theoretical model also predicts that dichogamy favors long-lived flowers, but empirical studies to test this prediction remain unexplored.Methods To examine the effect of floral sexual investment on floral longevity, we measured flower size together with pollen and ovule production in 37 sympatric flowering plants in a natural community. The duration of the female and male phase in 21 protandrous species and floral longevity of the other 16 adichogamous species were documented in the field.Important findings Floral longevity varied from 1 day to 15 days, while pollen number per flower varied from 643 to 710880 and ovule number per flower from 1 to 426 in the 37 species. Flower size was correlated with pollen production as well as ovule production. Floral longevity was positively related to pollen production but not to ovule production. Consistent with the prediction that dichogamy favors long-lived flowers, we found the floral longevity of protandrous species was significantly longer than that of adichogamous species. In the protandrous species, pollen production per flower was observed to be positively related to male duration, while ovule production was not related to female duration. Our analyses of variation in floral longevity and sexual investment among different species suggest that the floral sexual investment could be an intrinsic factor contributing to the selected floral longevity, particularly the male phase, and that high pollen production could potentially increase pollen removal, i.e. male productive success.     

RESPONSES OF FLORAL TRAITS TO SELECTION ON PRIMARY SEXUAL INVESTMENT IN SPERGULARIA MARINA: THE BATTLE BETWEEN THE SEXES

Two widespread assumptions underlie theoretical models of the evolution of sex allocation in hermaphroditic species: (1) resource allocations to male and female function are heritable; and (2) there is an intrinsic, genetically based negative correlation between male and female reproductive function. These assumptions have not been adequately tested in wild species, although a few studies have detected either genetic variation in pollen and ovule production per flower or evidence of trade-offs between male and female investment at the whole plant level. It may also be argued, however, that in highly autogamous, perfect-flowered plant taxa that exhibit genetic variation in gamete production, strong stabilizing selection for an efficient pollen:ovule ratio should result in a positive correlation among genotypes with respect to mean ovule and mean pollen production per flower. Here we report the results of a three-generation artificial selection experiment conducted on a greenhouse population of the autogamous annual plant Spergularia marina. Starting with a base population of 1200 individuals, we conducted intense mass selection for two generations, creating four selected lines (high and low ovule production per flower; high and low anther production per flower) and a control line. By examining the direct and correlated responses of several floral traits to selection on gamete production per flower, we evaluated the expectations that primary sexual investment would exhibit heritable variation and that resource-sharing, variation in resource-garnering ability, or developmental constraints mold the genetic correlations expressed among floral organs. The observed direct and correlated responses to selection on male and female gamete production revealed significant heritabilities of both ovule and anther production per flower and a significant negative genetic correlation between them. When plants were selected for increased ovules per flower over two generations, ovule production increased and anther production declined relative to the control line. Among plants selected for decreased anthers per flower, we observed a decline in anther production and an increase in ovule production relative to the control line. In contrast, the lines selected for low ovules per flower and for high anthers per flower exhibited no evidence for significant genetic correlations between male and female primary investment. Correlated responses to selection also indicate a genetically based negative correlation between the production of normal versus developmentally abnormal anthers (staminoid organs); a positive correlation between the production of ovules versus staminoid organs; and a positive correlation between the production of anthers and petals. The negative relationship between male versus female primary investment supports classical sex allocation theory, although the asymmetrical correlated responses to selection indicate that this relationship is not always expressed.     

Flower number and floral components in ten angiosperm species: an examination of assumptions about trade-offs in reproductive evolution

A common approach to modelling reproductive evolution in flowering plants includes an implicit assumption that module number and resource allocation per module follow an inverse hyperbolic trade-off. This assumption has not been thoroughly tested. In ten herbaceous and small woody species I examined phenotypic partial correlations between flower number (measured in relation to vegetative biomass) and each of three floral components: pollen number per flower, ovule number per flower, and corolla size. Significantly negative correlations between flower number and at least one of the floral components occurred in four of the ten species. These phenotypic correlations suggest the existence of true (genetically based) trade-offs, because environmental correlations are likely to be positive, but the significant negative relationships are linear except in one case. Thus, evolutionary tradeoffs involving flower number seem likely in some cases, but there is little to indicate that hyperbolic trade-offs are common. The phenotypic patterns investigated here cannot provide definitive answers about the form of trade-offs. Nonetheless, theoretical attention to the potential evolutionary consequences of trade-offs other than the implicit hyperbolic form is needed.     

Genetic constraints on floral evolution in a sexually dimorphic plant revealed by artificial selection

Sexual dimorphism is one of the most widespread and recognizable patterns of phenotypic variation in the biotic world. Sexual dimorphism in floral display is striking in the dioecious plant Silene latifolia, with males making many, small flowers compared to females. We investigated this dimorphism via artificial selection on two populations to determine whether genetic variation exists within populations for flower size and the extent of the between-sex correlation, whether a flower size and number trade-off exists within each sex, and whether pollen and ovule production vary with flower size. We selected for decreased flower size (calyx width) in females and increased flower size in males and measured the response to selection in size and correlated responses in flower dry mass, flower number, and pollen or ovule number per flower. Four bouts of selection in each of two selection programs were performed, for a total of three selection lines to decrease size, three to increase it, and two control lines. Flower size always significantly responded to selection and we always found a significant correlated response in the sex not under selection. Selection decreased but did not eliminate the sexual dimorphism in flower dry mass and number. A negative relationship between flower size and number within each sex was revealed. Whereas ovule number showed a significant correlated response to selection on flower size, pollen number did not. Our results indicate that although substantial additive genetic variation for flower size exists, the high between-sex genetic correlation would likely constrain flower size from becoming more sexually dimorphic. Furthermore, floral display within each sex is constrained by a flower size and number trade-off. Given this trade-off and lack of variation in pollen production with flower size, we suggest that sexual dimorphism evolved via sexual selection to increase flower number in males but not females.     

毛翠雀花花序内的性分配和繁殖成功

两性花植物花序内不同位置的性分配和繁殖成功一般存在差异,通常认为资源竞争、结构效应和交配环境是形成这种差异的主要原因.为了研究雄性和雌性繁殖资源在花序内不同位置间的最优分配问题,该文以青藏高原高寒草甸典型高山植物毛翠雀花为材料,通过比较花序内不同位置的花部特征和种子性状,对其花序内的性分配模式和雌性繁殖成功进行研究,并...