Plasticity in floral longevity and sex-phase duration of Lobelia siphilitica in response to simulated pollinator declines.

PREMISE: Pollinator declines can reduce the quantity and quality of pollination services, resulting in less pollen deposited on flowers and lower seed production by plants. In response to these reductions, plant species that cannot autonomously self-pollinate and thus are dependent on pollinators to set seed could plastically adjust their floral traits. Such plasticity could increase the opportunity for outcross pollination directly, as well as indirectly by affecting inflorescence traits. METHODS: To test whether plants can respond to pollinator declines by plastically adjusting their floral traits, we simulated declines by experimentally reducing pollinator access to Lobelia siphilitica plants and measuring two traits of early- and late-season flowers: (1) floral longevity; and (2) sex-phase duration. To test whether plasticity in these floral traits affected inflorescence traits, we measured daily display size and phenotypic gender. RESULTS: We found that experimentally reducing pollination did not affect female-phase duration, but did extend the male-phase duration of early-season flowers by 13% and the longevity of late-season flowers by 12.8%. However, plants with an extended male phase did not have a more male-biased phenotypic gender, and plants with an extended floral longevity did not have a larger daily display. CONCLUSIONS: Our results suggest that plants can respond to pollinator declines by plastically adjusting both the longevity and sex-phase duration of their flowers. If this plasticity increases the opportunity for outcross pollination, then it could be one mechanism by which pollinator-dependent plant species maintain seed production as pollinators decline.

Bee-Mediated Selection Favors Floral Sex Specialization in a Heterantherous Species: Strategies to Solve the Pollen Dilemma.

Animal-pollinated plants show a broad variation in floral morphology traits and gametophyte production within populations. Thus, floral traits related to plant reproduction and sexuality are usually exposed to pollinator-mediated selection. Such selective pressures may be even stronger in heterantherous and pollen flowers, in which pollen contributes to both bee feeding and pollination, overcoming the "pollen dilemma" or the inability to perform both functions simultaneously. We describe the phenotypic gender and sexual organ morphology of flowers in two populations of Macairea radula (Melastomataceae), a heterantherous and buzz-pollinated species with pollen flowers. We estimated selection gradients on these traits through female and male fitness components. Both populations showed sizeable phenotypic gender variation, from strict hermaphrodites to increased femaleness or maleness. We found a continuous variation in style and stamen size, and this variation was correlated with corresponding shape values of both sexual organs. We detected bee-mediated selection towards short and long styles through seed number and towards intermediate degrees of heteranthery through pollen removal in one population, and selection towards increased maleness through pollen dispersal in both populations. Our results suggest that bee-mediated selection favors floral sex specialization and stylar dimorphism in M. radula, optimizing reproductive success and solving the pollen dilemma.

Both small and large plants are likely to produce staminate (male) flowers in a hermaphrodite lily.

Resource allocation to female and male function may vary among individual plants in species with variable sex expression. Size-dependent sex allocation has been proposed in hermaphrodites, in which female-biased allocation may increase with plant size. In many hermaphrodites with large floral displays, however, later-produced flowers tend to be functionally male. This paradoxical relationship between female and male function and plant size remains poorly understood. The subalpine lily Lilium lankongense has individuals of three sexual types: males with only staminate flowers, hermaphrodites with only perfect flowers, and andromonoecious plants with both perfect and staminate flowers. Here we tested theoretical predictions of size-dependent sex allocation in L. lankongense by measuring plant height and flower number of individuals of each sex at five field sites in the mountainous region of Shangri-La, southwestern China. To investigate variation in phenotypic gender, we identified sex expression of 457 individuals one year later. Our investigation showed that male plants, which usually produced one flower, were significantly smaller than andromonoecious and hermaphrodite plants. In addition, the total flower numbers of andromonoecious and hermaphrodite plants increased significantly with plant size. Large individuals were more likely to produce terminal staminate flowers, as there were more flowers in andromonoecious than in hermaphrodite individuals. Non-flowered plants were significantly smaller than flowering ones. Perfect flowers had significantly larger petals and pistils than staminate flowers, but they did not differ in dry weight of stamens. Our findings indicate that when plants are small, the less costly sex is favored, consistent with the 'size-advantage hypothesis'. When plants are large, both female and male investments change isometrically, as later-produced flowers tend to be functionally male.

Plasticity in sex allocation in the plant Mercurialis annua is greater for hermaphrodites sampled from dimorphic than from monomorphic populations.

Plants are notoriously variable in gender, ranging in sex allocation from purely male through hermaphrodite to purely female. This variation can have both a genetic and an adaptive plastic component. In gynodioecious species, where females co-occur with hermaphrodites, hermaphrodites tend to shift their allocation towards greater maleness when growing under low-resource conditions, either as a result of hermaphrodites shifting away from an expensive female function, or because of enhanced siring advantages in the presence of females. Similarly, in the androdioecious plant Mercurialis annua, where hermaphrodites co-exist with males, hermaphrodites also tend to enhance their relative male allocation under low-resource conditions. Here, we ask whether this response differs between hermaphrodites that have been evolving in the presence of males, in a situation analogous to that supposed for gynodioecious populations, vs. those that have been evolving in their absence. We grew hermaphrodites of M. annua from populations in which males were either present or absent under different levels of nutrient availability and compared their reaction norms. We found that, overall, hermaphrodites from populations with males tended to be more female than those from populations lacking males. Importantly, hermaphrodites' investment in pollen and seed production was more plastic when they came from populations with males than without them, reducing their pollen production at low resource availability and increasing their seed production at high resource availability. These results are consistent with the hypothesis that plasticity in sex allocation is enhanced in hermaphrodites that have likely been exposed to variation in mating opportunities due to fluctuations in the frequency of co-occurring males.

Temporal variation in phenotypic gender and expected functional gender within and among individuals in an annual plant.

BACKGROUND AND AIMS: Adaptive explanations for variation in sex allocation centre on variation in resource status and variation in the mating environment. The latter can occur when dichogamy causes siring opportunity to vary across the flowering season. In this study, it is hypothesized that the widespread tendency towards declining fruit-set from first to last flowers on plants can similarly lead to a varying mating environment by causing a temporal shift in the quality (not quantity) of siring opportunities. METHODS: A numerical model was developed to examine the effects of declining fruit-set on the expected male versus female reproductive success (functional gender) of first and last flowers on plants, and of early- and late-flowering plants. Within- and among-plant temporal variation in pollen production, ovule production and fruit-set in 70 Brassica rapa plants was then characterized to determine if trends in male and female investment mirror expected trends in functional gender. KEY RESULTS: Under a wide range of model conditions, functional femaleness decreased sharply in the last flowers on plants, and increased from early- to late-flowering plants in the population. In B. rapa, pollen production decreased more rapidly than ovule production from first to last flowers, leading to a within-plant increase in phenotypic femaleness. Among plants, ovule production decreased from early- to late-flowering plants, causing a temporal decrease in phenotypic femaleness. CONCLUSIONS: The numerical model confirmed that declining fruit-set can drive temporal variation in functional gender, especially among plants. The discrepancy between observed trends in phenotypic gender in B. rapa and expected functional gender predicted by the numerical model does not rule out the possibility that male reproductive success decreases with later flowering onset. If so, plants may experience selection for early flowering through male fitness.

The roles of female and hermaphroditic flowers in the gynodioecious-gynomonoecious Silene littorea: insights into the phenology of sex expression.

Some gynodioecious species have intermediate individuals that bear both female and hermaphroditic flowers. This phenomenon is known as a gynodioecious-gynomonoecious sexual system. Gender expression in such species has received little attention in the past, and the phenologies of male and female functions have also yet to be explored. In this study, we examined variations in gender patterns, their effects on female reproductive success and sex expression in depth throughout the flowering period in two populations. The studied populations of Silene littorea contained mostly gynomonoecious plants and the number of pure females was very low. The gynomonoecious plants showed high variability in the total proportion of female flowers. In addition, the proportion of female flowers in each plant varied widely across the flowering season. Although there was a trend towards maleness, our measures of functional gender suggested that most plants transmit their genes via both pollen and ovules. Fruit set and seed set were not significantly different among populations; in contrast, flower production significantly varied between the two populations - and among plants - with consequent variation in total seed production. Conversely, gender and sex expression were similar in both populations. Plants with higher phenotypic femaleness did not have higher fruit set, seed set or total female fecundity. The mating environment fluctuated little across the flowering period, but fluctuations were higher in the population with low flower production. We therefore conclude that the high proportion of gynomonoecious individuals in our studied populations of S. littorea may be advantageous for the species, providing the benefits of both hermaphroditic and female flowers.

Effects of floral herbivory, limited pollination, and intrinsic plant characteristics on phenotypic gender in Sanicula arctopoides.

Sexual expression in hermaphroditic plants is often a function of environmental factors affecting individuals before or during flowering. I tested for the effects of floral herbivory and lack of pollination in early umbels on the relative proportions of hermaphroditic and staminate (male) flowers produced on later umbels by Sanicula arctopoides, a monocarpic, andromonoecious perennial. Neither floral herbivory or lack of early pollination had a significant effect on the ratio of the two floral morphs, but the probability of producing staminate flowers on late umbels was strongly and positively related to plant size measured just prior to floral initiation and prior to herbivory. Plant size was also negatively correlated with flowering date. I suggest that producing staminate flowers on late umbels should benefit large early-blooming plants more than small late-blooming plants because more mating opportunities occur during the period when these flowers release pollen. Although herbivory did not cause labile changes of sex, whole plant phenotypic gender was still strongly affected by various forms of treatment. Sex-biased herbivory or lack of pollination rendered plants more or less phenotypically male, depending on which tissues were affected. Deer and pollen-feeding mites preferentially remove male tissues while hymenopteran seed predators preferentially remove female tissues. I conclude that combinations of herbivores could have counteracting or compounding effects on plant gender, and these effects may change the rankings of male and female reproductive success within populations.