Flower Color Morphs Research Articles

Morphological and phenological variation of flower colour morphs in a wild population of Opuntia streptacantha (Cactaceae)

Background and aims – Opuntia s.s. (Cactaceae) is one of the most diverse genera in the subfamily Opuntioideae, with approximately 220 species. The considerable morphological and anatomical diversity among these species has resulted in a remarkable adaptative plasticity, evident in both intra- and interspecific variability. Our study system is Opuntia streptacantha, which has two flower colour morphs: yellow and orange. The objective is to determine if there are morphological differences in the reproductive and vegetative structures between floral morphs. Material and methods – We measured 8 cladode traits (n = 20 cladodes for each floral morph) and 17 flower traits (n = 30 flowers per morph), and reproductive phenology was recorded for both morphs to describe their phenophases (n = 10 individuals per morph). Key results and conclusion – We found that floral colour morphs of O. streptacantha showed significant differences mostly associated with flower traits. Principal component analysis revealed seven components that explained 80% of the total variation, namely total flower length, number of stamens, distance between anther and stigma, number of pollen grains, style length, equatorial diameter of the ovarian chamber, pericarp width, and number of areole lines. Some individuals of O. tomentosa were classified as floral morphs of O. streptacantha, not having a clear separation between the species. The phenology of the floral colour morphs showed a slight lag in their peak flowering and fruiting. Very high flowering synchrony was found for each floral morph and between them. The modifications found in the flowers of O. streptacantha may be associated with a possible hybridization with O. tomentosa favouring the appearance of the two floral morphs.

The ecological implications of intra- and inter-species variation in phenological sensitivity.

Plant-pollinator mutualisms rely upon the synchrony of interacting taxa. Climate change can disrupt this synchrony as phenological responses to climate vary within and across species. However, intra- and interspecific variation in phenological responses is seldom considered simultaneously, limiting our understanding of climate change impacts on interactions among taxa across their ranges. We investigated how variation in phenological sensitivity to climate can alter ecological interactions simultaneously within and among species using natural history collections and citizen science data. We focus on a unique system, comprising a wide-ranged spring ephemeral with varying color morphs (Claytonia virginica) and its specialist bee pollinator (Andrena erigeniae). We found strongly opposing trends in the phenological sensitivities of plants vs their pollinators. Flowering phenology was more sensitive to temperature in warmer regions, whereas bee phenology was more responsive in colder regions. Phenological sensitivity varied across flower color morphs. Temporal synchrony between flowering and pollinator activity was predicted to change heterogeneously across the species' ranges in the future. Our work demonstrates the complexity and fragility of ecological interactions in time and the necessity of incorporating variation in phenological responses across multiple axes to understand how such interactions will change in the future.

The effects of pollination, herbivory and autonomous selfing on the maintenance of flower colour variation in Silenelittorea.

Intraspecific flower colour variation has been generally proposed to evolve as a result of selection driven by biotic or abiotic agents. In a polymorphic population of Silene littorea with pink- and white-flowered plants, we studied pollinators, analysed flower colour perception and tested for differences in pollinator visitation. We also experimentally analysed pollinator limitation in fruit and seed set, and the degree of autonomous selfing. The incidence of florivory and leaf herbivory was compared over 3-4years. Silene littorea is mainly pollinated by bees and butterflies. Pollinators preferred pink flowers, which did not show pollinator limitation. On the contrary, white flowers showed pollinator limitation in fruit set. White-flowered plants had less floral display and higher levels of florivory than pink plants. Flower colour morphs of S. littorea can reproduce in the absence of pollinators by autonomous selfing, setting 20% and 12% of fruit and seeds in the pink morph and 27% and 20% in the white morph, respectively. Fruit set of white flowers produced by autonomous selfing did not differ from open-pollinated flowers. In conclusion, S. littorea is pollinated by insects of different orders that more frequently visit pink flowers, which is reflected in pollinator limitation of fruit set in white flowers. Moreover, this species has a mixed mating system in which both colour morphs can reproduce in the absence of pollinators by autonomous selfing, although white flowers mainly produce fruits by autogamy. We suggest that reproductive assurance by autonomous selfing helps to maintain flower colour polymorphism in this population.

Pollinator divergence and pollination isolation between hybrids with different floral color and morphology in two sympatric Penstemon species

Differential visitation of pollinators due to divergent floral traits can lead to reproductive isolation via assortative pollen flow, which may ultimately be a driving force in plant speciation, particularly in areas of overlap. We evaluate the effects of pollinator behavioral responses to variation of intraspecific floral color and nectar rewards, on reproductive isolation between two hybrid flower color morphs (fuchsia and blue) and their parental species Penstemon roseus and P. gentianoides with a mixed-pollination system. We show that pollinators (bumblebees and hummingbirds) exhibit different behavioral responses to fuchsia and blue morphs, which could result from differential attraction or deterrence. In addition to differences in color (spectral reflectance), we found that plants with fuchsia flowers produced more and larger flowers, produced more nectar and were more visited by pollinators than those with blue flowers. These differences influenced the foraging behavior and effectiveness as pollinators of both bumblebees and hummingbirds, which contributed to reproductive isolation between the two hybrid flower color morphs and parental species. This study demonstrates how differentiation of pollination traits promotes the formation of hybrid zones leading to pollinator shifts and reproductive isolation. While phenotypic traits of fuchsia and red flowers might encourage more efficient hummingbird pollination in a mixed-pollination system, the costs of bumblebee pollination on plant reproduction could be the drivers for the repeated shifts from bumblebee- to hummingbird-mediated pollination.

Lo esencial es invisible a los ojos (humanos): patrones UV explican la mayor tasa de visita de los polinizadores a las flores amarillas del arbusto Cytisus scoparius

A menudo, los polinizadores emplean los colores de las flores como senales indirectas del status de la recompensa. Sin embargo, los visitantes florales pueden percibir patrones del espectro cromatico invisibles para el ojo humano. Cytisus scoparius (retama) es un arbusto abundante en bosques perturbados del NO de la Patagonia que presenta variacion intra-especifica en el color de sus flores. Nosotros evaluamos si la mayor tasa de visita de los polinizadores a las flores amarillas, previamente documentada, es consecuencia de un patron UV mas atractivo en este morfo. Contamos cada 4 dias a lo largo de tres semanas el numero de visitas a flores amarillas y rojas rociadas con bloqueador solar (bloqueando el espectro UV), flores sin bloqueador (control) y flores con bloqueador en su pedicelo (para controlar posibles efectos indeseados del bloqueador, como el olor). El efecto del bloqueador solar en los petalos de las flores amarillas redujo la tasa de visita desde la primera medicion. Al final del muestreo, las flores amarillas con bloqueador en sus petalos fueron visitadas 7 veces menos que las flores control. Sin embargo, el efecto del bloqueador sobre los petalos de las flores rojas recien fue evidente al final del muestreo, reduciendo la tasa de visita solo 3 veces. Estos resultados sugieren que ambos morfos florales poseen patrones UV y que estos patrones atraen polinizadores, pero que su presencia estimula mas visitas en las flores amarillas que en las rojas. Esto puede deberse a que el espectro UV es mas contrastante en fondos amarillos que rojos. Finalmente, las flores amarillas y rojas con bloqueador solar en sus petalos tuvieron una tasa de visita similar, sugiriendo que los polinizadores se ven mas atraidos hacia las flores amarillas debido a la existencia de patrones UV y no por el color amarillo per se. Este trabajo resalta la importancia de analizar los patrones cromaticos invisibles al ojo humano para comprender mejor la relacion entre las senales florales y las tasas de visita de los polinizadores. https://doi.org/10.25260/EA.20.30.1.0.911

Flower Colour Polymorphism, Pollination Modes, Breeding System and Gene Flow in Anemone coronaria.

The flower colour of Anemone coronaria (Ranunculaceae) is a genetically inherited trait. Such intra-specific flower colour polymorphism might be driven by pollinators, other non-pollinating agents, or by abiotic factors. We investigated the genetic relations among red, white and purple-blue flower colour morphs growing in 10 populations of A. coronaria in Israel, in relation to their breeding system, pollination modes, differential perception by bees and visitors’ behaviour. Flowers of these three morphs differed in their reflectance that could be perceived by bees. Honeybees, solitary bees and flies demonstrated only partial preferences for the different colour morphs. No spontaneous self-pollination was found; however, fruit set under nets, excluding insects but allowing wind pollination, was not significantly lower than that of natural free pollinated flowers, indicating a potential role of wind pollination. Anemone coronaria flowers were visited by various insects, honeybees and Andrena sp. preferred the white and purple-blue morphs, while the syrphid flies preferred the white flowers. Thus, visitor behaviour can only partially explain the evolution or maintenance of the colour polymorphism. No significant genetic differences were found among the populations or colour morphs. Wind pollination, causing random gene flow, may explain why no significant genetic divergence was found among all studied populations and their colour morphs. The existence of monomorphic red populations, along other polymorphic populations, might be explained by linked resistance to aridity and/or grazing.

Appetitive reversal learning differences of two honey bee subspecies with different foraging behaviors.

We aimed to examine mechanistically the observed foraging differences across two honey bee, Apis mellifera, subspecies using the proboscis extension response assay. Specifically, we compared differences in appetitive reversal learning ability between honey bee subspecies: Apis mellifera caucasica (Pollman), and Apis mellifera syriaca (Skorikov) in a “common garden” apiary. It was hypothesized that specific learning differences could explain previously observed foraging behavior differences of these subspecies: A.m. caucasica switches between different flower color morphs in response to reward variability, and A.m. syriaca does not switch. We suggest that flower constancy allows reduced exposure by minimizing search and handling time, whereas plasticity is important when maximizing harvest in preparation for long winter is at a premium. In the initial or Acquisition phase of the test we examined specifically discrimination learning, where bees were trained to respond to a paired conditioned stimulus with an unconditioned stimulus and not to respond to a second conditioned stimulus that is not followed by an unconditioned stimulus. We found no significant differences among the subspecies in the Acquisition phase in appetitive learning. During the second, Reversal phase of the experiment, where flexibility in association was tested, the paired and unpaired conditioned stimuli were reversed. During the Reversal phase A.m. syriaca showed a reduced ability to learn the reverse association in the appetitive learning task. This observation is consistent with the hypothesis that A.m. syriaca foragers cannot change the foraging choice because of lack of flexibility in appetitive associations under changing contingencies. Interestingly, both subspecies continued responding to the previously rewarded conditioned stimulus in the reversal phase. We discuss potential ecological correlates and molecular underpinnings of these differences in learning across the two subspecies. In addition, in a supplemental experiment we demonstrated that these differences in appetitive reversal learning do not occur in other learning contexts.

Sexually-trimorphic interactions with colour polymorphism determine nectar quality in a herbaceous perennial

Amongst gynodioecious plant breeding systems, there can exist intermediate morphs with a reduction in their male function (i.e. reduced number of functional anthers). Along with this sexual trimorphism, plants can also show floral colour polymorphism. Such intricate mixtures of phenotypes within a species may have complex effects on floral rewards. Floral rewards are known to vary between sexually dimorphic species and to a lesser extent between colour morphs. However, the interactive effect of sexual trimorphism and colour polymorphism is unexplored. We measured nectar’s sugar content in the sexually trimorphic Geranium sylvaticum, a gynodioecious plant with a light/dark floral polymorphism. We found that nectar reward differed across genders and colour morphs. Results were not however consistent within the three genders; dark female and hermaphrodite flowers had higher sugar content than light morphs, whereas intermediate flowers did not. As expected, females and hermaphrodites had different nectar reward, with intermediate morphs being midway between the other genders. In intermediates, the sugar content was not related to the number of functional stamens. We show for the first time the existence of sex-specific differences between flower gender and colour morphs in nectar rewards. Our results demonstrate the importance of considering multiple and conflicting selection pressures to explain rewards.

Pollen tracking in the food-deceptive orchid Dactylorhiza sambucina showed no predominant switching behaviour of pollinators between flower colour morphs

The food-deceptive orchid Dactylorhiza sambucina is assumed to cheat its pollinators effectively by presenting two flower colour morphs. This hypothesis implies likely pollinator switches between the yellow- and purple-flowering plant individuals. However, pollen flow within and between morphs has never been tested by means of pollen tracking in a dimorphic population under field conditions. We studied a dimorphic population located in the southern “Wienerwald”-region to obtain frequencies of inter- and intra-morph pollinator switches. Pollinia were marked using dye powder to observe pollen flow, i.e. the spatial distribution of pollen, pollen export and deposition (i.e. male and female reproductive success) as well as the transport distances from donator to receptor plants. For analysing the switching behaviour of pollinators, we labelled yellow- and purple-flowering individuals morph-specifically using two different dye colours. In our study system, yellow-flowering plants were dominant (70% in 2006; 67% in 2014). We labelled 582 pollinia from yellow- and 239 from purple-flowering individuals reflecting the yellow-dominance (71%). In total, 473 marked pollinia were exported, of which 72.3% originated from yellow flowers. We found that movements of pollinators from yellow to yellow (YY) flowers dominate (93 of all 155 deposits of labelled pollen) the four possible pollination events by far. Even given the dominance of yellow-flowering plants in our study population, only 70 respective events (out of 155) would have been expected, if switching behaviour was by chance. Therefore, the assumption that pollinators alternate randomly between colour morphs was not supported by our results. The longest pollen transport distance observed was 237m. Moreover, 135 manually conducted cross-pollinations on 47 individuals were evaluated: seed viability analyses indicated no differences between the four possible crosses. Therefore, the dominance of the yellow morph at our study site could be the primary result of the most frequently observed cross-combination (i.e. YY).

Is there a hybridization barrier betweenGentiana luteacolor morphs?

In Gentiana lutea two varieties are described: G. lutea var. aurantiaca with orange corolla colors and G. lutea var. lutea with yellow corolla colors. Both color varieties co-occur in NW Spain, and pollinators select flower color in this species. It is not known whether a hybridization barrier exists between these G. lutea color varieties. We aim to test the compatibility between flower color varieties in G. lutea and its dependence on pollen vectors. Within a sympatric population containing both flower color morphs, we analyzed differences in reproductive success (number, weight, viability and germinability of seeds) depending on fertilization treatments (autogamy and xenogamy within variety and among varieties). We found a 93% reduction in number of seeds and a 37% reduction in seed weight respectively of autogamy treatments compared to xenogamy crossings. Additionally, reproductive success is higher within color varieties than among varieties, due to a 45% seed viability reduction on hybrids from different varieties. Our results show that G. lutea reproductive success is strongly dependent on pollinators and that a partial hybridization barrier exists between G. lutea varieties.

Flower colour and visitation rates of Costus arabicus support the ‘bee avoidance’ hypothesis for red‐reflecting hummingbird‐pollinated flowers

Summary Floral colour mediates plant–pollinator interactions by often signalling floral resources. In this sense, hummingbird‐pollinated flowers are frequently red‐coloured, and there are two tentative hypotheses to explain this pattern: 1. hummingbirds are attracted to red due its easier detection and 2. bees are sensorially excluded from red flowers. The second hypothesis is based on bees’ red colour blindness, which lead them to be less frequent and less important than hummingbirds as pollinators of red‐reflecting flowers. Here, we untangled the role of different flower traits mediating plant–pollinator interactions and empirically tested the above hypotheses. We chose Costus arabicus due to its synchronopatric white‐ and pink‐flowered individuals and its bee and hummingbird pollination system. Although pink flowers are not totally achromatic as pure red ones, they show an achromaticity degree that could drive bee exclusion. Specifically, we tested whether differences on red reflectance work attracting hummingbirds or excluding bees and the consequent implications for the plant's reproduction. Flower colour morphs of C. arabicus do differ neither in morphology nor in nectar sugar content. Moreover, white and pink flowers can be discriminated by the bees’ and hummingbirds’ colour vision system. Both groups are able to discriminate the red colour variation morph on the flower petals, the white flowers being more easily detected by bees and the pink flowers by hummingbirds. Bees preferentially visited the white flowers, whereas hummingbirds visited both colours at the same rate – both patterns corroborating the second hypothesis. Pollen loads deposited on stigmas did not differ between flower colour morphs, indicating that bees and hummingbirds play a similar role in the overall pollen deposition. However, bees are more likely to self‐pollinate than hummingbirds. Self‐pollination limits C. arabicus reproduction, and red‐reflecting flowers may be better pollinated by discouraging bee visitation. Therefore, the intraspecific colour variation is driving flowers to show colour‐related different levels of generalization. Our results support the ‘bee avoidance’ rather than the ‘hummingbird preference’ hypothesis. Sensory exclusion of bees seems to be the pressure for red‐reflecting flowers evolution, driving specialization in hummingbird‐pollinated flowers due to the costs of bee pollination on plant reproduction.

Pollinator-mediated competition influences selection for flower-color displacement in sympatric monkeyflowers.

When coflowering plant species share pollinators, pollinator-mediated competition may favor divergent floral characters associated with pollinator attraction. One potential outcome of this process is that sympatric populations will display increased divergence in floral traits compared with allopatric populations. We developed a new system to study the pattern and process of character displacement. In the central Sierra Nevada of California, USA, Mimulus bicolor is a spring wildflower with two flower-color morphs, one of which resembles coflowering M. guttatus. We documented a fine-scale geographic pattern of character displacement in sympatric and allopatric patches and, using experimental arrays, measured seed set in M. bicolor color morphs in the presence versus absence of M. guttatus. In sympatric arrays yellow, guttatus-like M. bicolor morphs had lower relative fitness (0.35 ± 0.05) and reduced conspecific pollen deposition compared with the distinct alternative morph, whereas in allopatric arrays yellow, guttatus-like morphs were occasionally strongly favored. Pollinator-mediated competition with M. guttatus is consistent with ecological character displacement in M. bicolor and likely contributes to a geographic pattern of character displacement.

Do queens of bumblebee species differ in their choice of flower colour morphs of Corydalis cava (Fumariaceae)?

Bumblebee queens require a continuous supply of flowering food plants from early spring for the successful development of annual colonies. Early in spring, Corydalis cava provides essential nectar and pollen resources and a choice of flower colour. In this paper, we examine flower colour choice (purple or white) in C. cava and verify the hypothesis that bumblebee queens differ in their choice of flower colour. A total of 10,615 observations of flower visits were made in spring 2011 and spring 2014 near Poznan, western Poland. Our results suggest that Bombus lucorum/cryptarum used purple flowers less, while Bombus terrestris used purple flowers more and Bombus hortorum showed no preference. Therefore, the colour morphs of C. cava are probably co-evolutionary adaptations to the development of another part of the insect community which has different colour preferences.

Comparison of floral properties and breeding system in dimorphicBuddleja delavayi(Scrophulariaceae)

AbstractIn this study, floral color, scent composition and emission rate, nectar property, pollinators, and breeding system of dimorphicBuddleja delavayiGagnep. were investigated. Flower color ofB. delavayiwas determined using a standard color chart and spectrophotometer, and two distinct color polymorphisms were observed having purple or white flowers. Floral scents ofB. delavayiwere collected using dynamic headspace adsorption and identified with coupled gas chromatography and mass spectrometry. In total, 28 compounds were identified from the flowers ofB. delavayi. The identified scents were divided into three chemical classes based on their biosynthetic origin: terpenes, fatty acid derivatives, and benzenoids. The scent profiles in all individuals were dominated by a few components, such as lilac aldehyde and alcohol, 4‐oxoisophorone, benaldehyde, and oxoisophorone oxide. Floral scent composition (benzenoids and terpenes) showed a significant difference between white and purple flower morphs. Flower color–flower scent associations inB. delavayiwere identified with two distinct scent profiles in the two color phenotypes. The studies of other floral characteristics (nectar, floral visitors, breeding system, and fruit set) indicated that floral scent emission rate, nectar volume, visitor visitation frequency, and natural fruit set were not significantly different between the two flower color morphs. Bagging experiments revealed that seed production ofB. delavayiis dependent mainly on honeybeeApis cerana. Lastly, this study implies that dimorphic floral color inB. delavayimay have been maintained by floral visitors and nectar guide color.

Reproductive biology and colour polymorphism in the food-deceptive Iris lutescens (Iridaceae)

Among the diversity of pollination strategies, food deception is intriguing because of the lack of rewards offered for the pollination services. Floral food deception has been frequently recorded in orchids; however, there is little evidence for food deception outside the Orchidaceae. One putative non-orchid candidate is the Mediterranean Iris lutescens, which displays an heritable polymorphism for flower colour, with yellow and purple morphs. Colour polymorphism is frequently thought to be maintained by negative frequency-dependent selection, where rare morphs are visited more frequently than common ones. Here, we present data on reproductive biology and pollination ecology of the species in the light of the deceptive pollination strategy and the maintenance of flower colour polymorphism. There was no difference in sex allocation and flowering phenology between morphs, with a blooming period early in spring. Both colour morphs are equally self-incompatible and they depend on insects for seed production. The most common visitors with pollen loads are small and large Apoids. These were observed foraging for non-existent nectar (rather than pollen) on Iris flowers. Most of them appear to learn to avoid Iris flowers as classically observed for rewardless species, and there was no evidence of an advantage for the rare morph. Instead, we found that in some populations, large bee pollinators appeared to prefer the most common morph (positive frequency-dependent selection). Iris lutescens appears to be a hitherto neglected but relevant candidate to investigate deceptive reproductive strategy and selective pressures in generalist plants.

Inflorescence scent, color, and nectar properties of “butterfly bush” (Buddleja davidii) in its native range

In this study, flower color, nectar properties, and inflorescence scent composition of eight natural and one introduced Buddleja davidii populations were investigated. Flower color of B. davidii was determined using the Royal Horticultural Society Color Chart and ranged from purple to white. Volume of nectar produced by a single flower ranged from 0.36μl to 0.64μl and total sugar concentration produced by inflorescence ranged from 17.0% to 33.5% in all populations. Floral nectar volume and sugar concentration were not significantly different between two flower color morphs in the B. davidii populations. Floral scents of B. davidii were collected using dynamic headspace adsorption and identified with coupled gas chromatography and mass spectrometry. In total, 33 compounds were identified from the inflorescences of B. davidii. The identified scents were divided into five chemical classes based on their biosynthetic origin: irregular terpenes, monoterpenoids, sesquiterpenoids, fatty acid derivatives, and benzenoids. The scent profiles in all populations were dominated by few components, such as: 4-oxoisophorone, E,E-α-farnesene, and 1-octen-3-ol. Given that inflorescence scents from natural and introduced individuals coming from the same population have discrepant chemical composition, we infer that phenotype plasticity may mediate floral scent composition. Based on the comparison of present and other data available on floral scent in B. davidii, we conclude that inflorescence scent may serve as a specific signal helping to attract pollinating butterflies to locate flowers as nectar sources, and may have evolved in conjunction with the sensory capabilities of butterflies and moths as a specific group of pollinators.

Herbivore pressure by weevils associated with flower color polymorphism in Geranium thunbergii (Geraniaceae)

Although floral herbivory has recently received increased attention as an important factor influencing plant reproduction, relatively little is known about how its frequency and intensity vary depending on traits of host plants. Here we report that herbivore pressure by a weevil, Zacladus geranii, is associated with a flower color polymorphism of Geranium thunbergii (Geraniaceae). Pink and white flower color morphs have been reported in G. thunbergii, and we found in a three-year field survey in multiple populations that, generally, adult weevils more preferentially visited white flowers than pink flowers. Consistently, we found more severe damage by weevil larvae in white flowers. Overall herbivore pressure for G. thunbergii varied strongly between populations, and the difference seems to be partly explained by the co-occurrence of a related plant species, Geranium yezoense, in a population, as weevils preferred it to both color morphs of G. thunbergii, thereby relaxing overall herbivore pressure for G. thunbergii. Nonetheless, despite such high variability, the preference of weevils for white morphs over pink morphs of G. thunbergii was found across multiple populations. We discuss possible mechanisms causing the association between flower color and herbivore preference as well as its evolutionary consequences.

Abiotic factors may explain the geographical distribution of flower colour morphs and the maintenance of colour polymorphism in the scarlet pimpernel

SummaryFlower colour polymorphism is traditionally attributed to pollinator selection although other factors, such as indirect selection on correlated traits, can play an important role.Lysimachia arvensisis a widespread annual species with two colour morphs differing in anthocyanin composition. We explored the hypothesis that colour polymorphism is maintained by selection related to environmental heterogeneity.Morph frequencies and environmental traits were recorded in 51 populations along a wide geographical range. To explore the existence of morph‐by‐environment interactions, we conducted an experimental study comparing the two morphs under treatments differing in water and light availability.A geographical pattern was found with a negative association between blue frequencies and latitude. The proportion of the blue morph increased with temperature and sunshine hours, but decreased with precipitation. Flowering onset and flower size differed between morphs and scarcely varied across treatments. In contrast, several fitness components such as germination, seedling survival, seedling mass and flower production showed important morph‐by‐environment interactions. The blue morph showed higher overall male and female fitness in all the treatment combinations excepting in sun‐wet conditions where the red morph had higher fitness.Synthesis. Our results indicate that the mechanism of selection on flower colour seems to be related to differences in fitness of both morphs due to abiotic factors. These differences could explain the geographical distribution of flower colour morphs and the maintenance of the colour polymorphism. The marked difference in flowering time between morphs leaves open the potential for assortative mating and speciation inLysimachia arvensis.

Tracing the Geographic Origins of Weedy Ipomoea purpurea in the Southeastern United States

Ipomoea purpurea (common morning glory) is an annual vine native to Mexico that is well known for its large, showy flowers. Humans have spread morning glories worldwide, owing to the horticultural appeal of morning glory flowers. Ipomoea purpurea is an opportunistic colonizer of disturbed habitats including roadside and agricultural settings, and it is now regarded as a noxious weed in the Southeastern US. Naturalized populations in the Southeastern United States are highly polymorphic for a number of flower color morphs, unlike native Mexican populations that are typically monomorphic for the purple color morph. Although I. purpurea was introduced into the United States from Mexico, little is known about the specific geographic origins of US populations relative to the Mexican source. We use resequencing data from 11 loci and 30 I. purpurea accessions collected from the native range of the species in Central and Southern Mexico and 8 accessions from the Southeastern United States to infer likely geographic origins in Mexico. Based on genetic assignment analysis, haplotype composition, and the degree of shared polymorphism, I. purpurea samples from the Southeastern United States are genetically most similar to samples from the Valley of Mexico and Veracruz State. This supports earlier speculation that I. purpurea in the Southeastern United States was likely to have been introduced by European colonists from sources in Central Mexico.

Pollinator response to flower color polymorphism and floral display in a plant with a single‐locus floral color polymorphism: consequences for plant reproduction

AbstractVariation in flower color, particularly polymorphism, in which two or more different flower color phenotypes occur in the same population or species, may be affected or maintained by mechanisms that depend on pollinators. Furthermore, variation in floral display may affect pollinator response and plant reproductive success through changes in pollinator visitation and availability of compatible pollen. To asses if flower color polymorphism and floral display influences pollinator preferences and movements within and among plants and fitness‐related variables we used the self‐incompatible species Cosmos bipinnatus Cav. (Asteraceae), a model system with single‐locus flower color polymorphism that comprises three morphs: white (recessive homozygous), pink (heterozygous co‐dominate), and purple (dominant homozygous) flowers. We measured the preferences of pollinators for each morph and constancy index for each pollinator species, pollination visitation rate, floral traits, and female fitness measures. Flower color morphs differed in floral trait measures and seed production. Pollinators foraged nonrandomly with respect to flower color. The most frequent morph, the pink morph, was the most visited and pollinators exhibited the highest constancy for this morph. Moreover, this morph exhibited the highest female fitness. Pollinators responded strongly to floral display size, while probed more capitulums from plants with large total display sizes, they left a great proportion of them unvisited. Furthermore, total pollinator visitation showed a positive relation with female fitness. Results suggest that although pollinators preferred the heterozygous morph, they alternate indiscriminately among morphs making this polymorphism stable.