The different forms of flowers – what have we learned since Darwin?

Darwin's book, The Different Forms of Flowers on Plants of the Same Species, has stimulated an extraordinary amount of original research since its publication in 1877. In his book, Darwin focused primarily on heterostylous reproductive systems in flowering plants, in which two or three reproductive morphs with reciprocal placement of anthers and stigmas occur in populations. These morphs are usually self‐incompatible and cross‐incompatible with individuals possessing the same reproductive morph. Many of the papers on heterostyly published since Forms of Flowers appeared have focused on the questions raised by Darwin about the evolution and function of heterostyly. Darwin's hypothesis that heterostyly promotes cross‐pollination between different morphs has been largely substantiated, despite the difficulties in finding the ideal experimental system to address this question. Heterostyly is now known to occur in many more plant families than at the time Forms of Flowers was published and, as expected, the heterostylous syndrome is now defined more broadly than in Darwin's time. The origin of heterostyly remains an area of active research, with hypotheses stressing either the evolution of heteromorphic self‐incompatibility as the first step in the evolution of this reproductive system or, alternatively, the evolution of the reciprocal features of floral morphology. Phylogenetic approaches, combined with studies on the physiological and molecular genetic basis of heterostyly, offer promise in helping to resolve questions about the origin of heterostyly. There is no doubt that heterostyly has evolved on multiple occasions and that self‐incompatibility associated with heterostyly is unrelated to the more common multi‐allelic self‐incompatibility systems found in monomorphic species. Further progress in understanding conditions favouring evolution of heterostyly will depend on an increased understanding of the relation between the reciprocal morphological features of the breeding system and the nature of self‐incompatibility. Almost a century and a half after the appearance of The Different Forms of Flowers on Plants of the Same Species, heterostyly remains an active area of research. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 249–261.     

Understanding plant reproductive diversity

Flowering plants display spectacular floral diversity and a bewildering array of reproductive adaptations that promote mating, particularly outbreeding. A striking feature of this diversity is that related species often differ in pollination and mating systems, and intraspecific variation in sexual traits is not unusual, especially among herbaceous plants. This variation provides opportunities for evolutionary biologists to link micro-evolutionary processes to the macro-evolutionary patterns that are evident within lineages. Here, I provide some personal reflections on recent progress in our understanding of the ecology and evolution of plant reproductive diversity. I begin with a brief historical sketch of the major developments in this field and then focus on three of the most significant evolutionary transitions in the reproductive biology of flowering plants: the pathway from outcrossing to predominant self-fertilization, the origin of separate sexes (females and males) from hermaphroditism and the shift from animal pollination to wind pollination. For each evolutionary transition, I consider what we have discovered and some of the problems that still remain unsolved. I conclude by discussing how new approaches might influence future research in plant reproductive biology.     

DECONSTRUCTING HETEROSTYLY: THE EVOLUTIONARY ROLE OF INCOMPATIBILITY SYSTEM,POLLINATORS, AND FLORAL ARCHITECTURE

Darwin's early work on heterostyly and related style polymorphisms (the presence of two or three style morphs within a population) generated much interest to understand how precise interactions between ecological and genetic mechanisms influence the evolution of floral diversity. Here we tested three key hypotheses proposed to explain the evolution of heterostyly: (i) the presence of self‐incompatibility; (ii) the role of pollinators in promoting dissasortative mating; and (iii) floral architecture, which restricts pollinators’ movements and ensures more exact pollen deposition on their bodies. We combined data from experiments, field observations, and published studies to test whether evolution of style polymorphism in Narcissus is driven by the incompatibility system, pollinator guilds, or floral architecture, within a phylogenetic framework. Neither differences in pollinator environment nor the presence of genetic self‐incompatibility were correlated with presence of style polymorphism. However, our results indicate that the evolution of style polymorphism was driven by the presence of a narrow and long floral tube.     

The evolution of polymorphic sexual systems in daffodils (Narcissus)

Narcissus, the daffodil genus, exhibits an unusual diversity of sexual systems, with populations that are monomorphic, dimorphic or trimorphic for style length. Associated with this variation are striking differences among species in floral morphology and pollination biology. This diversity provides an opportunity to investigate the evolution of mating polymorphisms, and to determine how floral morphology promotes transitions among sexual systems. Because of the absence of heteromorphic incompatibility in Narcissus, floral morphology plays a key role in governing patterns of outcrossed mating. Phylogenetic evidence indicates that stylar monomorphism is ancestral in the genus, with multiple origins of stylar polymorphism, including independent origins of stigma-height dimorphism, distyly and tristyly. Sexual polymorphisms have evolved only in lineages with narrow floral tubes that are pollinated by Lepidoptera and/or long-tongued bees. Populations of polymorphic Narcissus species are typically dominated by the long-styled morph and display imperfect reciprocity in the positions of sexual organs. These features are consequences of the unusual association between stylar polymorphism and a self-incompatibility system that permits intramorph mating.     

Orchid diversity: an evolutionary consequence of deception?

The Orchidaceae are one of the most species-rich plant families and their floral diversity and pollination biology have long intrigued evolutionary biologists. About one-third of the estimated 18,500 species are thought to be pollinated by deceit. To date, the focus has been on how such pollination evolved, how the different types of deception work, and how it is maintained, but little progress has been made in understanding its evolutionary consequences. To address this issue, we discuss here how deception affects orchid mating systems, the evolution of reproductive isolation, speciation processes and neutral genetic divergence among species. We argue that pollination by deceit is one of the keys to orchid floral and species diversity. A better understanding of its evolutionary consequences could help evolutionary biologists to unravel the reasons for the evolutionary success of orchids.     

Darwin's Galápagos finches in modern biology

One of the classic examples of adaptive radiation under natural selection is the evolution of 15 closely related species of Darwin''s finches (Passeriformes), whose primary diversity lies in the size and shape of their beaks. Since Charles Darwin and other members of the Beagle expedition collected these birds on the Galápagos Islands in 1835 and introduced them to science, they have been the subjects of intense research. Many biology textbooks use Darwin''s finches to illustrate a variety of topics of evolutionary theory, such as speciation, natural selection and niche partitioning. Today, as this Theme Issue illustrates, Darwin''s finches continue to be a very valuable source of biological discovery. Certain advantages of studying this group allow further breakthroughs in our understanding of changes in recent island biodiversity, mechanisms of speciation and hybridization, evolution of cognitive behaviours, principles of beak/jaw biomechanics as well as the underlying developmental genetic mechanisms in generating morphological diversity. Our objective was to bring together some of the key workers in the field of ecology and evolutionary biology who study Darwin''s finches or whose studies were inspired by research on Darwin''s finches. Insights provided by papers collected in this Theme Issue will be of interest to a wide audience.     

Heterostyly accelerates diversification via reduced extinction in primroses

The exceptional species diversity of flowering plants, exceeding that of their sister group more than 250-fold, is especially evident in floral innovations, interactions with pollinators and sexual systems. Multiple theories, emphasizing flower–pollinator interactions, genetic effects of mating systems or high evolvability, predict that floral evolution profoundly affects angiosperm diversification. However, consequences for speciation and extinction dynamics remain poorly understood. Here, we investigate trajectories of species diversification focusing on heterostyly, a remarkable floral syndrome where outcrossing is enforced via cross-compatible floral morphs differing in placement of their respective sexual organs. Heterostyly evolved at least 20 times independently in angiosperms. Using Darwin''s model for heterostyly, the primrose family, we show that heterostyly accelerates species diversification via decreasing extinction rates rather than increasing speciation rates, probably owing to avoidance of the negative genetic effects of selfing. However, impact of heterostyly appears to differ over short and long evolutionary time-scales: the accelerating effect of heterostyly on lineage diversification is manifest only over long evolutionary time-scales, whereas recent losses of heterostyly may prompt ephemeral bursts of speciation. Our results suggest that temporal or clade-specific conditions may ultimately determine the net effects of specific traits on patterns of species diversification.     

The interplay between inflorescence development and function as the crucible of architectural diversity

Background

Most angiosperms present flowers in inflorescences, which play roles in reproduction, primarily related to pollination, beyond those served by individual flowers alone. An inflorescence''s overall reproductive contribution depends primarily on the three-dimensional arrangement of the floral canopy and its dynamics during its flowering period. These features depend in turn on characteristics of the underlying branching structure (scaffold) that supports and supplies water and nutrients to the floral canopy. This scaffold is produced by developmental algorithms that are genetically specified and hormonally mediated. Thus, the extensive inflorescence diversity evident among angiosperms evolves through changes in the developmental programmes that specify scaffold characteristics, which in turn modify canopy features that promote reproductive performance in a particular pollination and mating environment. Nevertheless, developmental and ecological aspects of inflorescences have typically been studied independently, limiting comprehensive understanding of the relations between inflorescence form, reproductive function, and evolution.

Scope

This review fosters an integrated perspective on inflorescences by summarizing aspects of their development and pollination function that enable and guide inflorescence evolution and diversification.

Conclusions

The architecture of flowering inflorescences comprises three related components: topology (branching patterns, flower number), geometry (phyllotaxis, internode and pedicel lengths, three-dimensional flower arrangement) and phenology (flower opening rate and longevity, dichogamy). Genetic and developmental evidence reveals that these components are largely subject to quantitative control. Consequently, inflorescence evolution proceeds along a multidimensional continuum. Nevertheless, some combinations of topology, geometry and phenology are represented more commonly than others, because they serve reproductive function particularly effectively. For wind-pollinated species, these combinations often represent compromise solutions to the conflicting physical influences on pollen removal, transport and deposition. For animal-pollinated species, dominant selective influences include the conflicting benefits of large displays for attracting pollinators and of small displays for limiting among-flower self-pollination. The variety of architectural components that comprise inflorescences enable diverse resolutions of these conflicts.     

Wind of change: new insights on the ecology and evolution of pollination and mating in wind-pollinated plants

Background

The rich literature that characterizes the field of pollination biology has focused largely on animal-pollinated plants. At least 10 % of angiosperms are wind pollinated, and this mode of pollination has evolved on multiple occasions among unrelated lineages, and hence this discrepancy in research interest is surprising. Here, the evolution and functional ecology of pollination and mating in wind-pollinated plants are discussed, a theoretical framework for modelling the selection of wind pollination is outlined, and pollen capture and the occurrence of pollen limitation in diverse wind-pollinated herbs are investigated experimentally.

Scope and Conclusions

Wind pollination may commonly evolve to provide reproductive assurance when pollinators are scarce. Evidence is presented that pollen limitation in wind-pollinated plants may not be as common as it is in animal-pollinated species. The studies of pollen capture in wind-pollinated herbs demonstrate that pollen transfer efficiency is not substantially lower than in animal-pollinated plants as is often assumed. These findings challenge the explanation that the evolution of few ovules in wind-pollinated flowers is associated with low pollen loads. Floral and inflorescence architecture is crucial to pollination and mating because of the aerodynamics of wind pollination. Evidence is provided for the importance of plant height, floral position, and stamen and stigma characteristics in promoting effective pollen dispersal and capture. Finally, it is proposed that geitonogamous selfing may alleviate pollen limitation in many wind-pollinated plants with unisexual flowers.Key words: Wind pollination, reproductive assurance, pollen limitation, geitonogamy, sex allocation, inflorescence architecture, mating systems     

All in an afternoon: mixed breeding system in one-day lasting flowers of Hypericum elodes L. (Hypericaceae)

Knowledge about mixed mating systems can improve our understanding of the evolutionary dynamics of reproductive systems. Here we report a study of the floral and reproductive biology of Hypericum elodes, an Atlantic-European soft-water pools specialist which shows a floral architecture consistent with both self- and cross-pollination. Controlled pollination experiments were performed in a natural population during three consecutive years. Marked flowers were monitored until fruit production, and laboratory germination experiments were conducted with the seeds produced. Plants were self-compatible (SCI>0.75), however, compared with selfing, cross-pollination enhanced fruit-set, seed-set and seedling growth, but not seed germination. Inbreeding depression (δ) was mild in the pre-dispersal stages (δ = 0.22 for fruit set, 0.18 for seed set and 0.13 for seed mass), low for germination percentage (δ = 0.003) and mild for seedling growth (δ = 0.23). The breeding system of H. elodes promotes outcrossing and assures reproductive success by means of competitive autogamy. Our results suggest a mixed mating strategy for the studied population, characterized by mild inbreeding depression (cumulative δ = 0.57), highlighting the benefit of this reproductive mode in unpredictable habitat, as the typical shallow-water meadows where H. elodes grows.     

Darwin's cross-promotion hypothesis and the evolution of stylar polymorphism

There is growing appreciation that the ecological factors which impact on rates of pollen transfer can contribute significantly to reproductive trait evolution in plants. In heterostylous species, several studies support Darwin's claim that the reciprocal positions of stigmas and anthers enhance inter‐morph mating in comparison to intra‐morph mating and thus the maintenance of the polymorphism. In this study, we evaluate the relative importance of intra‐morph and inter‐morph pollen transfers in Narcissus assoanus, a species with dimorphic variation in style length but non‐reciprocity of anther positions. This stigma‐height dimorphism represents a transitional stage in theoretical models of the evolution of distyly. Seed set variation on recipient plants with donor plants of a single morph in experimental arrays in a natural population illustrate that inter‐morph cross‐pollination is more efficient that intra‐morph cross‐pollination as a result of high rates of pollen transfer from long‐styled to short‐styled plants. The observed rates of pollen transfer satisfy the theoretical conditions for the establishment of a stigma‐height dimorphism in an ancestral monomorphic long‐styled population in pollen‐limited situations. These results provide experimental evidence for the Darwinian hypothesis that enhanced inter‐morph cross‐pollination facilitates not only the maintenance of heterostyly but also the establishment of transitional forms implicated in the evolution of this polymorphism.     

The role of a mixed mating system in the reproduction of a Mediterranean subshrub (Fumana hispidula, Cistaceae)

Knowledge about mixed mating systems can improve our understanding of the evolutionary dynamics of reproductive systems. Here we report a study of the pollination system (floral and reproductive biology, pollen limitation and stigmatic pollen load, floral visitors and inbreeding depression) of Fumana hispidula, a Mediterranean subshrub belonging to a species group with a strong selfing tendency. Autonomous self-pollination, hand self- and hand cross-pollination, open pollination and controls yielded fruits (0.28, 0.65, 0.68, 0.38, and 0.67, respectively); however, autonomous self-pollination resulted in the lowest fruit set. All individuals were fully self-compatible but we found great inter-individual variation in autonomous self-pollination ability, which was probably related to a variable expression of herkogamy degree. Inbreeding depression was low (0.040 for fruit set, 0.015 for seed set and ?0.026 for seed mass). The pollen supplementation experiment did not reveal pollen limitation and pollinators were seen visiting the flowers during the observation periods. These results support the idea that F. hispidula has a mixed mating strategy, which represents a successful reproduction mode in their patchy habitats.     

Floral biology and mechanisms of spontaneous self‐pollination in five neotropical species of Gentianaceae

Cross‐ and self‐fertilization in angiosperms are regulated by several factors, and a knowledge of the mechanism and time of spontaneous self‐pollination offers opportunities for a better understanding of the evolution of mating systems and floral traits. The floral biology of five species of Gentianaceae found in high‐altitude neotropical grassland is presented, with emphasis on the mechanisms that promote spontaneous self‐pollination. A presumed floral Batesian mimicry system is suggested between the rare and rewardless Zygostigma australe and Calydorea campestris, a species of Iridaceae with pollen‐flowers, pollinated by syrphids and bees. The floral morphology of the other four gentian species points to three different pollination syndromes: melittophily, phalaenophily and ornithophily. However, with the exception of the nocturnal Helia oblongifolia, flowers are nectarless and appear to exhibit non‐model deceptive mechanisms, providing similar floral cues to some sympatric rewarding species with the same syndrome. The similar mechanism of spontaneous self‐pollination in Calolisianthus pedunculatus, Calolisianthus pendulus and H. oblongifolia (Helieae) is based on the stigmatic movements towards the anthers. Selfing is promoted by movements of the style/stigma and of the corolla in Deianira nervosa and Z. australe (Chironieae), respectively. The movements of stamens, style and stigma during anthesis seem to be the most common method of spontaneous self‐pollination in angiosperms. It is suggested that the evolution of delayed spontaneous self‐pollination would be more expected in those taxa with dichogamous flowers associated with herkogamy. Such a characteristic is frequent in long‐lived flowers of certain groups of Asteridae, which comprise most documented cases of autonomous selfing. Thus, the presence of dichogamy associated with herkogamy (which supposedly evolved as a result of selection to promote both separation of male and female functions and the efficient transfer of cross pollen) may be the first step in the adaptive evolution of delayed selfing to provide reproductive assurance. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 357–368.     

Variation in floral longevity in the genus Leptosiphon: mating system consequences

Pollination or fertilisation trigger floral senescence in a wide range of flowering plants, and yet little attention has been given to the implications of this phenomenon to mating system evolution. We examined the effects of pollination on floral senescence in the genus Leptosiphon. Species in the genus exhibit a wide range of breeding systems. In all cases, compatible pollination induced senescence; emasculated flowers lived longer than hand‐outcrossed flowers. In the self‐compatible species, Leptosiphon acicularis and L. bicolor, and in one highly selfing population of L. jepsonii, unmanipulated flowers had reduced longevity compared to emasculated flowers, suggesting that autonomous self‐pollination limits floral longevity in these species. Limited floral longevity in these highly selfing taxa may reduce opportunities for male outcross success, representing a possible source of selection on the mating system. In turn, the mating system might influence how selection acts on floral longevity; obligately outcrossing taxa are expected to benefit from longer floral longevities to maximise opportunities for pollination, while selfing taxa might benefit from earlier floral senescence to reduce resource expenditure. Overall, the longevity of unpollinated flowers increased with the level of outcrossing in the genus Leptosiphon. Our results taken together with those of a previous study and similar results in other species suggest that floral longevity may represent a largely unexamined role in mating system evolution.     

Ecology and evolution of plant�Cpollinator interactions

Background

Some of the most exciting advances in pollination biology have resulted from interdisciplinary research combining ecological and evolutionary perspectives. For example, these two approaches have been essential for understanding the functional ecology of floral traits, the dynamics of pollen transport, competition for pollinator services, and patterns of specialization and generalization in plant–pollinator interactions. However, as research in these and other areas has progressed, many pollination biologists have become more specialized in their research interests, focusing their attention on either evolutionary or ecological questions. We believe that the continuing vigour of a synthetic and interdisciplinary field like pollination biology depends on renewed connections between ecological and evolutionary approaches.

Scope

In this Viewpoint paper we highlight the application of ecological and evolutionary approaches to two themes in pollination biology: (1) links between pollinator behaviour and plant mating systems, and (2) generalization and specialization in pollination systems. We also describe how mathematical models and synthetic analyses have broadened our understanding of pollination biology, especially in human-modified landscapes. We conclude with several suggestions that we hope will stimulate future research. This Viewpoint also serves as the introduction to this Special Issue on the Ecology and Evolution of Plant–Pollinator Interactions. These papers provide inspiring examples of the synergy between evolutionary and ecological approaches, and offer glimpses of great accomplishments yet to come.Key words: Floral traits, generalization and specialization, global change, male fitness, mating systems, multiple paternity, plant–pollinator networks, pollen and gene dispersal, pollinator behaviour, pollination syndromes, pollination webs, self-fertilization     

The evolution of plant reproductive systems: how often are transitions irreversible?

Flowering plants are characterized by striking variation in reproductive systems, and the evolutionary lability of their sexual traits is often considered a major driver of lineage diversification. But, evolutionary transitions in reproductive form and function are never entirely unconstrained and many changes exhibit strong directionality. Here, I consider why this occurs by examining transitions in pollination, mating and sexual systems, some of which have been considered irreversible. Among pollination systems, shifts from bee to hummingbird pollination are rarely reversible, whereas transitions from animal to wind pollination are occasionally reversed. Specialized pollination systems can become destabilized through a loss of pollinator service resulting in a return to generalized pollination, or more commonly a reliance on self-pollination. Homomorphic and heteromorphic self-incompatibility systems have multiple origins but breakdown to self-compatibility occurs much more frequently with little evidence for subsequent gains, at least over short time-spans. Similarly, numerous examples of the shift from outcrossing to predominant self-fertilization are known, but cases of reversal are very limited supporting the view that autogamy usually represents an evolutionary dead-end. The evolution of dioecy from hermaphroditism has also been considered irreversible, although recent evidence indicates that the occurrence of sex inconstancy and hybridization can lead to the origin of derived sexual systems from dioecy. The directionality of many transitions clearly refutes the notion of unconstrained reproductive flexibility, but novel adaptive solutions generally do not retrace earlier patterns of trait evolution.     

青藏高原及周边高山地区的植物繁殖生态学研究进展

青藏高原及周边高山地区孕育了极为丰富的植物多样性资源, 研究该地区植物如何顺利完成繁殖过程有助于我们理解植物对典型高山环境的进化和适应机制。该文综述了青藏高原地区高山植物在资源分配、繁殖方式、花部特征演化等方面的研究进展, 包括全球气候变化对植物繁殖特征的影响, 以及一些新技术和新方法在本研究领域的应用。在高山地区限制性环境中, 随海拔升高, 繁殖分配通常表现出增大的趋势, 其中投入到雄性资源的比例上升, 但具体的资源分配模式还要取决于植株的交配系统、个体大小、生活史特征、遗传特性以及环境中的资源有效性等。面对资源和传粉的双重限制, 植物在不同繁殖方式之间存在权衡, 当传粉者稀少时, 克隆繁殖和自交有利于繁殖保障; 而有性繁殖和异交能够提高种子的质量和后代的遗传多样性, 从而在复杂多变的气候条件下有利于种群的维持。因此, 不同繁殖方式的结合以及泛化的传粉互作网络可能是应对高山限制性环境的最优选择。花部特征的演化主要受到当地传粉者的选择压力, 但是外来传粉者、植食者、盗蜜者以及非生物环境(如温度、雨水和紫外辐射等)对花部性状的影响越来越受到重视。近年来, 青藏高原因其脆弱性和对气候变化的高度敏感性而在全球气候变化研究中备受关注, 以全球变暖和氮沉降增加为显著特征的全球气候变化正在直接或间接地影响着该地区高山植物的繁殖特征。气候变化影响植物和传粉者的物候并引起物种的迁移, 最终将导致植物与传粉者的时空不匹配。植物通过改变花部特征(花展示、花冠结构、花报酬的数量和质量)来响应气候变化, 这可能会改变其传粉者的类型、数量和访花行为, 从而最终影响植物的繁殖成功。3D打印和高通量测序等新技术和新方法的应用有助于促进植物繁殖生态学研究的进一步发展。3D打印的花能够精确控制其形态构造, 可以用于研究精细的花部特征变化对于传粉者行为的影响, 在此基础上与人工饲养的传粉者结合使用, 有助于进一步研究传粉者介导的花部特征演化。随着高通量测序技术的发展, 植物繁殖生态学领域, 尤其是花部特征演化的许多重要问题的潜在机制得以深入研究。该文最后提出了目前研究中需要注意的问题以及值得深入研究的发展方向。     

Pollination,mating and reproductive fitness in a plant population with bimodal floral‐tube length

Mating patterns and natural selection play important roles in determining whether genetic polymorphisms are maintained or lost. Here, we document an atypical population of Lapeirousia anceps (Iridaceae) with a bimodal distribution of floral‐tube length and investigate the reproductive mechanisms associated with this pattern of variation. Flowers were visited exclusively by the long‐proboscid fly Moegistorhynchus longirostris (Nemestrinidae), which exhibited a unimodal distribution of proboscis length and displayed a preference for long‐tubed phenotypes. Despite being visited by a single pollinator species, allozyme markers revealed significant genetic differentiation between open‐pollinated progeny of long‐ and short‐tubed phenotypes suggesting mating barriers between them. We obtained direct evidence for mating barriers between the floral‐tube phenotypes through observations of pollinator foraging, controlled hand pollinations and measurements of pollen competition and seed set. Intermediate tube‐length phenotypes produced fewer seeds in the field than either long‐ or short‐tubed phenotypes. Although floral‐tube length bimodality may not be a stable state over long timescales, reproductive barriers to mating and low ‘hybrid’ fitness have the potential to contribute to the maintenance of this state in the short term.     

广西蜘蛛抱蛋(Aspidistra retusa)的传粉生物学研究

蜘蛛抱蛋属植物的花部结构丰富多样,且常常贴地表开花,但其传粉生物学研究鲜有报道。广西蜘蛛抱蛋(Aspidistra retusa)是广西特有植物,为揭示该物种的自然传粉机制,在蜘蛛抱蛋属世界分布和分化中心的广西境内,开展了广西蜘蛛抱蛋开花物候、访花昆虫及繁育系统的野外观测研究。结果表明:广西蜘蛛抱蛋的花部结构中雄蕊高于雌蕊,但自交不亲和,为异花传粉;双翅目瘿蚊属成虫(Cecidomyia sp.,Cecidomyiidae,Diptera)为其专性传粉者,作为回报,广西蜘蛛抱蛋为瘿蚊提供理想的交配场所,同时提供大量的花粉供雌瘿蚊取食以补充生殖所需能量,并为受精卵的孵化以及幼虫的发育提供舒适的环境。该研究用实地现场观察第一手数据验证了前人有关蜘蛛抱蛋属植物瘿蚊传粉的推测,为中国蜘蛛抱蛋属植物传粉生物学研究的首次报道,然而蜘蛛抱蛋属植物花部结构极具多样性,应存在更多样的传粉方式,还有待更深入的调查研究。