Floral Color Polymorphism and Reproductive Success in Annatto (Bixa orellana L.)

Floral color polymorphism of annatto (Bixa orellana L.) offers a wide range of colors that are maintained in the population by either pollinators or non pollinator agents of selection. In the present study, maintenance of different floral colors was analyzed in relation to reproductive success of Bixa orellana. The different floral petal colors (white, amaranth rose, petunia purple or cobalt violet) were determined from selected plants with reflectance spectrophotometry. Phenotypic measures of other floral traits, female reproductive success, seed set, seed output and seed weight also revealed variation between different floral morphs. Records on seed set varied significantly for different floral color morphs. Maximum fruit maturation (58 %) was observed in amaranth rose and least fruit maturation (25 %) in the white morph. Seed set data indicates pollinators’ preference for more intensely colored flowers. This preference may be due to ability of the pollinators to distinguish the morphs through differentially reduced sensitivity at the green wavelengths. In flowers which received fewer insect visits, polymorphism might be maintained by self fertilization. The color morphs showed differences in Random Amplified Polymorphic DNA (RAPD) profile indicating a genetic basis for floral color variation and consequent differences in seed set. Out of 88 bands generated with nine operon primers, 70 were polymorphic. The present study provides valuable information on the influence of petal color on maternal fitness in B. orellana.     

Flower Color Polymorphism in Rhododendron cyanocarpum (Ericaceae), an Endangered Alpine Species Endemic to NW Yunnan,China

Rhododendron cyanocarpum is a narrow endemic species with pink and white floral color. In the present study, to investigate the significance of petal color morphs, we examined color morph frequencies, petal color reflectance and other associated floral characters, effective pollinators, visitation frequencies, and fruit production in the field. In all surveyed known populations, plants with pink color morph dominanted and comprised 77%-100% of individuals. Two peaks at 430 nm and 650 nm were found in the petal color reflectance of pink flowers, and only one peak at 430 nm was found in the reflectance spectrum of white flowers. In addition, color morphs were also associated with colors of style and stigma, lengths of corolla, calyx and pedicel, the closest distance between stigma and stamen, but not with style length and nectar production. Moreover, higher visitation frequency of their shared pollinators (bumblebees) and fruit production were observed of pink flowers than white flowers. Despite a briefly temporal and spacial study, we suggest that color morph frequencies, visit frequencies of bumblebees and fruit production, all favor to be stablilizing selection for the pink color morph.     

滇西北特有植物蓝果杜鹃的花色多态性研究(英文)

蓝果杜鹃(Rhododendron cyanocarpum)为大理苍山特有的濒危植物,有粉色和白色两种花冠类型。为了探讨该物种花色多态性的意义,本研究调查了粉色花和白色花植株在已知的各居群的分布频率、花冠的反射光谱及其它的花部特征、有效传粉者及其访花频率与结实情况。结果表明:粉色花植株在所有调查的居群中占优势(77%~100%)。粉色花的花冠反射光谱在430 nm和650 nm有两个峰,而白色花只在430 nm有一个反射峰。同时,花特征如:花柱与柱头颜色、花冠长度、花萼长度、花梗长度以及雌雄蕊最短距离,两种花冠存在显著差异。另外,尽管熊蜂作为这两种花冠的主要传粉者,但粉红花的访花频率以及自然条件下的结实情况显著高于白色花。本研究结果推测粉红色花可能受到了稳定性选择的作用。     

Nonrandom Composition of Flower Colors in a Plant Community: Mutually Different Co-Flowering Natives and Disturbance by Aliens

When pollinators use flower color to locate food sources, a distinct color can serve as a reproductive barrier against co-flowering species. This anti-interference function of flower color may result in a community assembly of plant species displaying mutually different flower colors. However, such color dispersion is not ubiquitous, suggesting a variable selection across communities and existence of some opposing factors. We conducted a 30-week study in a plant community and measured the floral reflectances of 244 species. The reflectances were evaluated in insect color spaces (bees, swallowtails, and flies), and the dispersion was compared with random expectations. We found that co-existing colors were overdispersed for each analyzed pollinator type, and this overdispersion was statistically significant for bees. Furthermore, we showed that exclusion of 32 aliens from the analysis significantly increased the color dispersion of native flowers in every color space. This result indicated that aliens disturbed a native plant–pollinator network via similarly colored flowers. Our results demonstrate the masking effects of aliens in the detection of color dispersion of native flowers and that variations in pollinator vision yield different outcomes. Our results also support the hypothesis that co-flowering species are one of the drivers of color diversification and affect the community assembly.     

Apis cerana japonica discriminates between floral color phases of the oriental orchid, Cymbidium floribundum

Foragers of the Japanese honeybee (Apis cerana japonica) were attracted by flowers of an oriental orchid (Cymbidium floribundum) and were observed to carry the pollinia on their scutella. After the removal of pollinia from the flowers, their labial color changed from white to reddish brown. Both artificial removal of pollinia and ethrel treatment of the flowers also induced this labial color change. Labia in color-changed flowers showed a decreased reflectance of wavelengths less than 670 nm compared to control intact flower. Both reflectance irradiance spectra and ultraviolet photographs showed that only the nectar guide in white (unchanged) flowers reflected ultraviolet light, and that this reflectance decreased with labial color change. Dual choice experiments showed that the honeybee foragers preferentially visited flowers having white labia rather than reddish brown. We suggest that Japanese honeybees discriminate between the floral phases of C. floribundum using color vision.     

PHOTOGRAPHIC VISUALIZATION OF FLORAL COLORS AS PERCEIVED BY HONEYBEE POLLINATORS

An inexpensive photographic technique for visualizing the ultraviolet and visible wavelengths perceived by honeybees is described. Using a standard daylight-balanced color slide film and illumination from blacklight and filtered daylight fluorescent lamps, a recording balance was achieved which approximates the spectral sensitivity of the honeybee eye. The technique was used to illustrate floral features among Rudbeckia species and among color morphs of Phlox. The Rudbeckia have inflorescences that are similar in visible coloration but distinctive in ultraviolet patterning and Phlox color morphs are distinctive in visible coloration but similar in ultraviolet patterning. The efficacy of the technique was judged from comparison with in vivo reflectance spectra of the floral subjects. Generally, photographic visualizations of entomophilous flowering plants portray only the ultraviolet or the visible components of floral coloration. This technique emphasizes the importance of considering the entire spectrum of floral colors relevant to most insect pollinators.     

FReD: the floral reflectance database--a web portal for analyses of flower colour

Background

Flower colour is of great importance in various fields relating to floral biology and pollinator behaviour. However, subjective human judgements of flower colour may be inaccurate and are irrelevant to the ecology and vision of the flower''s pollinators. For precise, detailed information about the colours of flowers, a full reflectance spectrum for the flower of interest should be used rather than relying on such human assessments.

Methodology/Principal Findings

The Floral Reflectance Database (FReD) has been developed to make an extensive collection of such data available to researchers. It is freely available at http://www.reflectance.co.uk. The database allows users to download spectral reflectance data for flower species collected from all over the world. These could, for example, be used in modelling interactions between pollinator vision and plant signals, or analyses of flower colours in various habitats. The database contains functions for calculating flower colour loci according to widely-used models of bee colour space, reflectance graphs of the spectra and an option to search for flowers with similar colours in bee colour space.

Conclusions/Significance

The Floral Reflectance Database is a valuable new tool for researchers interested in the colours of flowers and their association with pollinator colour vision, containing raw spectral reflectance data for a large number of flower species.     

Trapped: Assessing Attractiveness of Potential Food Sources to Bumblebees

Unrewarding artificial flowers that trapped approaching bumblebees were used here for the first time to assess the effects of several floral characteristics on floral attractiveness to bumblebees that never obtained food from flowers. Floral size and floral scent had no discernable effect. In a comparison between two colors (white and blue) and two shapes (radial and square), choice proportions for blue radial flowers were significantly greater than chance. Our proposed method is an alternative to prior training, with food associated either with visual or olfactory stimuli, which is unnecessary to obtain floral preferences by free-flying bumblebees exploring potential food sources.     

Use of CC traps with different trap base colors for silverleaf whiteflies (Homoptera: Aleyrodidae), thrips (Thysanoptera: Thripidae), and leafhoppers (Homoptera: Cicadellidae)

During 1996, 1997, and 1999, studies were conducted in cotton, sugar beets, alfalfa, yardlong bean, and peanut fields to compare insect catches in CC traps equipped with different trap base colors. The studies were conducted in southwestern United States, China, and India. The nine colors, white, rum, red, yellow, lime green, spring green, woodland green (dark green), true blue, and black, varied in spectral reflectance in the visible (400-700 nm) and near-infrared (700-1050 nm) portions of spectrum. Lime green, yellow, and spring green were the three most attractive trap base colors for silverleaf whitefly, Bemisia argentifolii Bellows & Perring, and leafhopper, Empoasca spp. adults. The three trap base colors were moderately high in the green, yellow, and orange spectral regions (490-600 nm), resembling the spectral reflectance curve of the abaxial (underleaf) surfaces of green cotton leaves. True blue and white were the most attractive trap base colors for western flower thrips, Frankliniella occidentalis (Pergande), adults. The true blue and white trap bases were moderately high in the blue spectral region (400-480 nm).     

花颜色和花气味的量化研究方法

花颜色和花气味是花部构成的重要内容。在已开展的传粉生态学研究中对二者的报道主要是描述性的,而其量化研究可以为揭示传粉机制提供有力的实验证据。本文主要介绍了花颜色的测量和标定方法,包括比色卡、分光色差仪和便携式光谱仪等;花气味的采集方法,包括动态顶空套袋-吸附采集法、吸附-溶剂洗脱法和固相微萃取法等;花气味的检测和分析方法,包括气相色谱-质谱联用仪分析和电子鼻型超速气相色谱仪分析等;以及昆虫行为学实验方法,包括气相色谱-昆虫触角电位联用技术、Y型嗅觉仪和飞行箱实验等。科研人员可以根据实验材料的特点和实验目的选择适合的量化研究方法。     

Blue light controls solar tracking by flowers of an alpine plant

In at least 18 plant families, leaves or flowers can maintain a specific orientation with respect to diurnal movements of the sun. Previous work on heliotropic leaves has demonstrated that blue light (400–500nm) provides the cue for their tracking response. Floral heliotropism occurs in several families of arctic and alpine plants, but the spectral sensitivity of the response has not been studied previously. Moreover, no studies on the spectral sensitivity of any heliotropism have been conducted on wild plants growing in their natural habitat. Working under field conditions, we used coloured acrylic filters to determine whether heliotropism by flowers of the snow buttercup (Ranunculus adoneus) is responsive to broad-band blue or red light. Flowers were able to orient towards the sun under boxes made entirely of blue-transmitting filters and in red-transmitting boxes having a single blue side that faced the sun. In these treatments, solar tracking ability was not significantly different from that observed in adjacent control flowers. In contrast, the precision of solar orientation was significantly reduced in red-transmitting boxes and red boxes with a single blue side oriented away from the sun. In the early morning, flowers covered by red-transmitting boxes failed to orient in the direction of sunrise, suggesting that this floral response, unlike that seen in some heliotropic leaves, lacks a residual‘memory’ for previous solar movements.     

Breeding System and pollination of selected plants endemic to Juan Fernandez Islands

We conducted field studies on the Juan Fernández Islands flora on the breeding system of 25 endemic species from 17 families. We recorded data on flower features, pollen and ovule number, pollen/ovule ratio, pollen size, self-compatibility, floral visitors, and pollination. Flowers are mostly hermaphrodite, inconspicuous, small, and green. Six species are dioecious. Over 80% of the cosexual species are self compatible. However, many species are dichogamous (mostly protandrous); thus, even the self-compatible species may require pollen transfer. Selfing through geitonogamy seems to be the most common system, and several species express mixed breeding systems. Floral visitors are uncommon to rare, except for two hummingbird species (one native and one endemic) that visit five species we studied. In more than 300 h of observation of flowers over three field seasons, we detected only 23 native insect visits representing ten species (Diptera, Lepidoptera, and Coleoptera). One species each of an introduced ant and an introduced bee were also observed on some flowers, all near the single human settlement of San Juan Bautista. Wind directly moving pollen, or indirectly via shaking the flowers, is the most important pollen distribution mechanism. The majority of the wind-pollinated species bear some typical anemophilous features, but also others not characteristic of wind pollination, that presumably represent the condition of their biotically pollinated ancestors. Floral features often reflect ancestral reproductive systems, so floral biology studies of oceanic islands in particular must be done with cognizance of presumed ancestral forms, because the observed characters can be misleading.     

Chromatic and achromatic stimulus discrimination of long wavelength (red) visual stimuli by the honeybee Apis mellifera

It has long been assumed that bees cannot see red. However, bees visit red flowers, and the visual spectral sensitivity of bees extends into wavelengths to provide sensitivity to such flowers. We thus investigated whether bees can discriminate stimuli reflecting wavelengths above 560 nm, i.e., which appear orange and red to a human observer. Flowers do not reflect monochromatic (single wavelength) light; specifically orange and red flowers have reflectance patterns which are step functions, we thus used colored stimuli with such reflectance patterns. We first conditioned honey bees Apis mellifera to detect six stimuli reflecting light mostly above 560 nm and found that bees learned to detect only stimuli which were perceptually very different from a bee achromatic background. In a second experiment we conditioned bees to discriminate stimuli from a salient, negative (un-rewarded) yellow stimulus. In subsequent unrewarded tests we presented the bees with the trained situation and with five other tests in which the trained stimulus was presented against a novel one. We found that bees learned to discriminate the positive from the negative stimulus, and could unambiguously discriminate eight out of fifteen stimulus pairs. The performance of bees was positively correlated with differences between the trained and the novel stimulus in the receptor contrast for the long-wavelength bee photoreceptor and in the color distance (calculated using two models of the honeybee colors space). We found that the differential conditioning resulted in a concurrent inhibitory conditioning of the negative stimulus, which might have improved discrimination of stimuli which are perceptually similar. These results show that bees can detect long wavelength stimuli which appear reddish to a human observer. The mechanisms underlying discrimination of these stimuli are discussed. Handling Editor: Lars Chittka.     

Specialized pollination in the African milkweed Xysmalobium orbiculare: a key role for floral scent in the attraction of spider-hunting wasps

Specialized pollination by prey-hunting wasps is poorly documented in rewarding plants. Furthermore, the mechanisms of achieving specialization are not clear since flowers typically produce exposed nectar and have no morphological adaptations (such as long spurs) to exclude non-pollinating visitors. We investigated the pollination of Xysmalobium orbiculare and explored the functional roles of floral scent and nectar in attracting pollinators and deterring nectar robbers. Floral visitor observations showed that this milkweed is visited almost exclusively by pompilid wasps in the genus Hemipepsis. These wasps were the only insects to carry pollinia, and a cage experiment confirmed their effectiveness in removing and inserting pollinia on flowers. Hand-pollinations showed that plants are genetically self-incompatible and thus reliant on pollinators for seed set. Palatability experiments with honeybees showed that nectar is distasteful to non-pollinating insects and is therefore likely to play a functional role in deterring nectar thieves. Choice experiments in the field showed that the wasp pollinators are attracted primarily by floral scent rather than visual cues. Analysis of spectral reflectance of flowers revealed that flowers are dull colored and are unlikely to stand out from the background vegetation. We conclude that X. orbiculare is specialized for pollination by spider-hunting wasps in the genus Hemipepsis and utilizes floral scent to selectively attract its pollinators and unpalatable nectar to deter non-pollinating visitors.     

Ultraviolet reflectance mediates pollinator visitation in Mimulus guttatus

Floral colors are widely believed to be an adaptation to attract pollinators. Recently, our understanding of floral reflectance has broadened to include colors that are beyond the spectrum that human eyes can perceive (such as ultraviolet (UV) reflectance), yet we still know relatively little about which plant species reflect UV light or its effectiveness in attracting pollinators. We investigated the effect of UV reflectance in Mimulus guttatus in a number of different populations in British Columbia, Canada. We found that M. guttatus had distinct regions of the corolla where UV light was reflected and absorbed. When we manipulated the degree of contrast between the reflection and absorption area, we found that pollinator visitation was severely disrupted, in terms of frequency and foraging patterns observed. Despite the bright yellow (bee‐green) coloration and visible nectar guides in M. guttatus, we conclude that UV reflectance is critical in pollinator attraction.     

Flower Color, Hummingbird Pollination, and Habitat Irradiance in Four Neotropical Forests1

Pollinator visual systems differ considerably among broad groupings such as bees, bats, and birds, and it has been proposed that factors shaping the diversity of flower color in tropical plants include differences in pollinator perceptual abilities. Within the pollinators of the Neotropics, one major difference between taxa is that hummingbirds perceive color well across a broad range of wavelengths from 300–660 nm whereas most bees perceive color well over a narrower range spanning 300–550 nm. Thus, hummingbirds can see red and other long‐wavelength reflection much better than bees. Another factor that could potentially influence flower color in tropical forests is the difference in light availability among habitats such as gaps, canopy, and forest understory. I conducted a survey of floral color in four Neotropical forests using a portable spectroradiometer to provide an unbiased measure of color reflectance. The primary pollinator agents and light habitats of each plant species were classified using primary literature or accounts of direct observations by experts. Flower color was not influenced by differences in light availability between open and closed habitats but was influenced by pollinator visual systems. Specifically, insect flowers reflected across a broad range of the spectrum but hummingbird flowers reflected mostly long‐wavelength light (typically median wavelength <585 nm). Thus, hummingbird‐pollinated flowers are not tuned specifically to hummingbird color sensitivity but instead may decrease conspicuousness to bees and other insects that have poor visual sensitivity to long‐wavelength color.     

IS FLORAL SPECIALIZATION AN EVOLUTIONARY DEAD‐END? POLLINATION SYSTEM TRANSITIONS IN RUELLIA (ACANTHACEAE)

Pollination systems frequently reflect adaptations to particular groups of pollinators. Such systems are indicative of evolutionary specialization and have been important in angiosperm diversification. We studied the evolution of pollination systems in the large genus Ruellia. Phylogenetic analyses, morphological ordinations, ancestral state reconstructions, and a character mapping simulation were conducted to reveal key patterns in the direction and lability of floral characters associated with pollination. We found significant floral morphological differences among species that were generally associated with different groups of floral visitors. Floral evolution has been highly labile and also directional. Some specialized systems such as hawkmoth or bat pollination are likely evolutionary dead-ends. In contrast, specialized pollination by hummingbirds is clearly not a dead-end. We found evidence for multiple reverse transitions from presumed ancestral hummingbird pollination to more derived bee or insect pollination. These repeated origins of insect pollination from hummingbird-pollinated ancestors have not evolved without historical baggage. Flowers of insect-pollinated species derived from hummingbird-pollinated ancestors are morphologically more similar to hummingbird flowers than they are to other more distantly related insect-pollinated flowers. Finally, some pollinator switches were concomitant with changes in floral morphology that are associated with those pollinators. These observations are consistent with the hypothesis that some transitions have been adaptive in the evolution of Ruellia.     

Pollination of Schisandra henryi (Schisandraceae) by female, pollen-eating Megommata species (Cecidomyiidae, Diptera) in south-central China

BACKGROUND AND AIMS: The mutualistic interaction between insects and flowers is considered to be a major factor in the early evolution of flowering plants. The Schisandraceae were, until now, the only family in the ANITA group lacking information on pollination biology in natural ecosystems. Thus, the objective of this research was to document the pollination biology and breeding system of Schisandra henryi. METHODS: Field observations were conducted in three populations of S. henryi and the floral phenology, floral characters and insect activities were recorded. Floral fragrances were sampled in the field and analysed using TCT-GC-MS. Floral thermogenesis was measured with a TR-71U Thermo Recorder. Pollen loads and location of pollen grains on insect bodies (including the gut) were checked with a scanning electron microscope and under a light microscope. KEY RESULTS: Schisandra henryi is strictly dioecious. Male flowers are similar to female flowers in colour, shape, and size, but more abundant than female flowers. The distance between tepals and the androecium or gynoecium is narrow. Neither male nor female flowers are fragrant or thermogenic. Schisandra henryi is pollinated only by adult female Megommata sp. (Cecidomyiidae, Diptera) that eat the pollen grains as extra nutrition for ovary maturation and ovipositing. Both male and female flowers attract the pollinators using similar visual cues and thus the female flowers use deceit as they offer no food. CONCLUSIONS: Schisandra henryi exhibits a specialized pollination system, which differs from the generalized pollination system documented in other ANITA members. Pollen is the sole food resource for Megommata sp. and the female flowers of S. henryi attract pollinators by deceit. This is the first report of predacious gall midges utilizing pollen grains as a food source. The lack of floral thermogenesis and floral odours further enforces the visual cues by reducing attractants for other potential pollinators.     

Morning floral heat as a reward to the pollinators of the Oncocyclus irises

Relationships between flowering plants and their pollinators are usually affected by the amount of reward, mainly pollen or nectar, offered to pollinators by flowers, with these amounts usually positively correlated with floral display. The large Oncocyclus iris flowers, despite being the largest flowers in the East Mediterranean flora, are nectarless and have hidden pollen. No pollinators visit the flowers during daytime, and these flowers are pollinated only by night-sheltering solitary male bees. These iris flowers are partially or fully dark-colored, suggesting that they gather heat by absorbing solar radiation. Here we test the hypothesis that the dark-colored flowers of the Oncocyclus irises offer heat reward to their male solitary bee pollinators. Floral temperature was higher by 2.5°C than ambient air after sunrise. Solitary male bees emerged earlier after sheltering in Oncocyclus flowers than from other experimental shelter types. Pollination tunnels facing east towards the rising sun hosted more male bees than other aspects. We suggest that floral heat reward can explain the evolution of dark floral colors in Oncocyclus irises, mediated by the pollinators’ behavior.     

FLORAL ONTOGENY IN CYCLAMEN PERSICUM ‘F-1 ROSEMUNDE ROSE’ (PRIMULACEAE)

Floral ontogeny was examined in Cyclamen persicum ‘F-1 Rosemunde Rose’ using a combination of light and scanning electron microscopy. The leaf plastochron index (LPI), earlier calculated for leaf elongation, was used to determine the length of each stage of floral development. LPI will provide a useful tool for selecting flowers of a given stage from large plant populations or from plants where flowers are small or inaccessible during early ontogenetic stages. Most features of floral development are similar to those previously described for other primulaceous genera. The petal-stamen relationship, however, is unusual; stamens arise through periclinal cell divisions in the adaxial surface layers of common petal-stamen primordia. Anatomical evidence suggests that the placenta is formed both by appendicular initials which give rise to the ovules and ventral carpellary bundles, and receptacular cells which form some, if not all, of the central axis.