Structure of the Cyperaceae Inflorescence

This work presents the basics for interpreting the adult inflorescence structure in Cyperaceae. It provides an analysis of the variations of the synflorescence and inflorescence structure in the family. Three types of synflorescence may be recognized in this family: a synflorescence with a foliate stem, a terminal inflorescence and a variable number of lateral inflorescences; a synflorescence with a foliate stem and only the terminal inflorescence; and a synflorescence with a scape and a terminal inflorescence. Variations in the structure and form of the inflorescences are related to variations in inflorescence branching, inflorescence homogenization degree, presence or absence of the distal part of the inflorescence, phyllotaxis, inflorescence position, types of bracts and leaves subtending branches, elongation of inflorescence internodes and spikelet structure. These variations are correlated with some of the developmental processes that give origin to the inflorescence.     

Organographic and ontogenetic studies on the inflorescence ofLespedeza cuneata (Dum.-Cours.) G. Don (Leguminosae)

Structure of inflorescence and its variation were organographically and ontogenetically studied inLespedeza cuneata (Dum.-Cours.) G. Don. An axillary inflorescence of the species forms a compound inflorescence which is composed of three or four component inflorescences. Each component inflorescence bears four (rarely six), three, two, or one flowers. Based on the arrangement of inflorescence phyllomes, the component inflorescence with four flowers is interpreted as a pseudoraceme bearing two shortened lateral shoots (partial inflorescences) each of which has two flowers. The component inflorescence with one flower appears to be terminated by the flower and to compose the cyme. Organographic observations revealed that the terminally located flower is not truly terminal, but axillary in origin. Ontogenetic observations showed that the apices of component inflorescence and partial inflorescence exist in early developmental stages in spite of variation in the form of component inflorescence. The terminally located flower in the cyme-like inflorescence was thus demonstrated to be laterally borne on the partial inflorescence axis. The component inflorescence composing the cyme-like one inL. cuneata is a reduced form in the number of partial inflorescences and of flowers from the pseudoraceme. The cyme-like inflorescence inL. cuneata resembles the inflorescence ofKummerowia.     

The effect of flower position on male and female reproductive success in a deceptively pollinated tropical orchid

In many plants, including orchids, differential fruit set along the inflorescence has been attributed to pollinator behaviour. For instance, the pollinator, moving up the inflorescence, becomes satiated with the resources and leaves before visiting the upper flowers. Consequently, the pollinators do not visit flowers as frequently higher up the inflorescence. Alternatively, flower size may vary along the inflorescence, making pollination ineffective as flowers decrease in size. I tested for the presence of differential pollination along the inflorescence in a pollinator-limited tropical epiphyte, Lepanthes rupestris Stimson, and determined the likely cause of the observed pattern. As this species has inflorescences with sequential flowering, pollinator behaviour, moving up the inflorescence as in synchronous multiflowering inflorescences, can be discounted as an explanation for differential fruit set. Fruit set is shown to be more frequent at the base of the inflorescence, but male reproductive success through pollinarium removal is basically independent of flower position. Moreover, cross-pollination by hand at variable flower positions along the inflorescence results in equal fruit set, suggesting that resources are not limiting and cannot explain the cause of differential fruit production along the inflorescence in natural populations. Furthermore, flower size is shown to diminish along the inflorescence, suggesting that the pollinator(s) may be ineffective at depositing the pollinarium in the smaller higher flowers. Consequently, pollinator behaviour and its interaction with flower size, and not resource limitation, is likely to be the main cause of differential fruit set along the inflorescence in L. rupestris .  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 405–410.     

Water Deficit and Inflorescence Development in Zea mays L.--The Role of the Developing Tassel

In the normal pattern of development of Zea mays (cv. Iochief)a single mature female inflorescence is produced at node 7.A brief episode of water deficit at the time of terminal maleinflorescence initiation induced the subsequent developmentof two to three mature female inflorescences at nodes 5–7.This growth of the inflorescences at lower nodes was accompaniedby a marked inhibition of the growth of the terminal male inflorescence.Removal of either the developing terminal inflorescence or ofthe axillary inflorescence at node 7 at this time also promotedthe growth of the lower axillary inflorescences. The growthof these inflorescences was further stimulated by a period ofwater deficit when only the inflorescence at node 7 was removed,but removal of the male inflorescence abolished the capacityof these inflorescences to respond to the water deficit Excisionof the male inflorescence immediately before or immediatelyafter the period of water deficit produced the same response.It is concluded that this response of the lower axillary inflorescencesto water deficit is mediated through an effect on the developingterminal male inflorescence. Zea mays, water deficit, inflorescence development, tassel, correlative inhibition     

关于一些植物学术语的中译等问题(三)

(1)确定rhizome的中文译名"根状茎"符合此术语的定义,同时认为另一中文译名"根茎"不符合有关定义,且易引起误解,应予废弃。(2)介绍了在中国植物学文献中稀见的2种属于有限花序类的花序类型,有限伞形花序和有限头状花序。根据有关欧美专家的花序研究,介绍了在中国植物学文献中放在无限花序类的隐头花序和柔荑花序系由聚伞花序演化而出,而应属于有限花序类的论断;同时,作者提出楼梯草属梨序楼梯草组的雄隐头花序系由同属的骤尖楼梯草组的有限头状花序演化而出的论点。     

Proteomic Analyses of Three Inflorescence Styles of Castor (<i>Ricinus communis</i> L.) at Different Developmental Stages

Castor (Ricinus communis L.) is one of ten oil crops in the world and has complex inflorescence styles. Generally, castor has three inflorescence types: single female inflorescence (SiFF), standard female inflorescence (StFF) and bisexual inflorescence (BF). StFF is realized as a restorer line and as a maintainer line, which was applied to castor hybrid breeding. However, the developmental mechanism of the three inflorescences is not clear. Therefore, we used proteomic techniques to analyze different inflorescence styles. A total of 72 diferentially abundant protein species (DAPs) were detected. These DAPs are primarily involved in carbon and energy metabolism and carbon fixation in the photosynthetic organism pathway. The results showed that DAPs are involved in photosynthesis to control the distribution of imported carbohydrates and exported photoassimilates and thus affect the inflorescence development of castor. In addition, these DAPs are also involved in cysteine and methionine metabolism. Quantitative real-time PCR (qRT-PCR) results demonstrated that the proteomics data collected in this study were reliable. Our findings indicate that the carbon cycle and amino acid metabolism influence the inflorescence development of castor.     

Trophotagma Enrichment Axes in Poaceae

This review is intended: (1) to interpret and characterize morphological variations observed in the structure of the enrichment axes, located below the terminal inflorescence in Poaceae; and (2) to study the relationship between the intensity of development of such axes and the size of terminal inflorescence. An important reduction in the development of the terminal inflorescence is generally accompanied by a significant development of enrichment axes. It is necessary to adequately characterize these enrichment axes, differentiating them from the terminal inflorescence. Since the intensive development of enrichment axes in synflorescences of many grass genera has caused misinterpretations of the inflorescence structure, to include them as parts of the terminal inflorescence.     

Reproductive developmental complexity in the African oil palm (Elaeis guineensis, Arecaceae)

Species of the palm family (Arecaceae) are remarkably diverse in their inflorescence and floral morphologies, which make them a particularly interesting group for studies of reproductive development and its evolution. Using light and scanning electron microscopy, we describe inflorescence and flower development in the African oil palm Elaeis guineensis from the initiation of the inflorescence meristem to flower maturity. In mature palms, the inflorescence develops over 2-3 years and is characterized by individual stages within which differentiation may be either relatively slow, as in the case of early inflorescence meristem development, or rapid, as in the case of flower organogenesis. The female inflorescence bears floral triads composed of single pistillate flowers flanked by two abortive staminate flowers, whereas the male inflorescence contains single functional staminate flowers. This suggests a possible evolutionary movement from an ancestral hermaphrodite inflorescence form containing fully functional floral triads to the situation of temporal dioecy observed at present. Wild type flowers are compared to those bearing an epigenetic homeotic abnormality, known as mantled, involving an alteration of the identity of the organs in the fertile and sterile androecium.     

Insights into panicoid inflorescence evolution

Inflorescence forms can be described by different combinatorial patterns of meristem fates (indeterminate versus determinate). In theory, the model predicts that any combination is possible. Whether this is true for grasses is unknown. In this paper, the subfamily Panicoideae s.s. (panicoid grasses) was chosen as the model group to investigate this aspect of grass inflorescence evolution. We have studied the inflorescence morphology of 201 species to complement information available in the literature. We have identified the most recurrent inflorescence types and character states among panicoids. Using multivariate approaches, we have indentified correlations among different inflorescence character states. By phylogenetic reconstruction methods we have inferred the patterns of panicoid inflorescence evolution. Our results demonstrate that not all theoretical combinatorial patterns of variation are found in panicoids. The fact that each panicoid lineage has a unique pattern of inflorescence evolution adds an evolutionary component to combinatorial model.     

barren inflorescence2 regulates axillary meristem development in the maize inflorescence

Organogenesis in plants is controlled by meristems. Shoot apical meristems form at the apex of the plant and produce leaf primordia on their flanks. Axillary meristems, which form in the axils of leaf primordia, give rise to branches and flowers and therefore play a critical role in plant architecture and reproduction. To understand how axillary meristems are initiated and maintained, we characterized the barren inflorescence2 mutant, which affects axillary meristems in the maize inflorescence. Scanning electron microscopy, histology and RNA in situ hybridization using knotted1 as a marker for meristematic tissue show that barren inflorescence2 mutants make fewer branches owing to a defect in branch meristem initiation. The construction of the double mutant between barren inflorescence2 and tasselsheath reveals that the function of barren inflorescence2 is specific to the formation of branch meristems rather than bract leaf primordia. Normal maize inflorescences sequentially produce three types of axillary meristem: branch meristem, spikelet meristem and floral meristem. Introgression of the barren inflorescence2 mutant into genetic backgrounds in which the phenotype was weaker illustrates additional roles of barren inflorescence2 in these axillary meristems. Branch, spikelet and floral meristems that form in these lines are defective, resulting in the production of fewer floral structures. Because the defects involve the number of organs produced at each stage of development, we conclude that barren inflorescence2 is required for maintenance of all types of axillary meristem in the inflorescence. This defect allows us to infer the sequence of events that takes place during maize inflorescence development. Furthermore, the defect in branch meristem formation provides insight into the role of knotted1 and barren inflorescence2 in axillary meristem initiation.     

Optimal foraging in hummingbirds: Rule of movement between inflorescences

The movements of hummingbirds between inflorescences of scarlet gilia (Ipomopsis aggregata) were studied. These movements exhibited the following patterns: (1) Although the hummingbirds appeared to avoid moving to the previous inflorescence, no significant correlation was found between the directions of successive inter-inflorescence movements. (2) The frequency distribution of inter-inflorescence flight distances was found to be leptokurtic. (3) The hummingbirds were more likely to move to an inflorescence the larger and/or closer it was. (4) The hummingbirds moved to inflorescences of greatest apparent size (i.e. ratio of number of flowers available to distance from present inflorescence) more often than they moved to the largest inflorescence, the closest infloresence, or the inflorescence estimated to yield the greatest rate of energy gain. (5) The frequency distribution of moves to the inflorescence having the ith greatest apparent size is well fitted by a geometric distribution. This is consistent with the hummingbrids choosing the inflorescence of greatest apparent size (excluding the previous inflorescence) from within some scanning sector. These movement patterns are consistent with the expectations of optimal foraging theory only if the hummingbirds cannot or do not determine the directions of possible inflorescences relative to the direction of arrival at the present inflorescence and if they cannot assess independently the sizes and distances of possible inflorescences.     

Inflorescence structures and evolution in subfamily Chloridoideae (Gramineae)

Inflorescence structures of 81 species and two subspecies (representing 61 genera) of the Chloridoideae have been investigated using stereo microscopy (SM). Inflorescences of the Chloridoideae are true polytelic inflorescences. Thirteen inflorescence subtypes are distinguished based on modes of the truncation and the homogenization. These are categorized into four basic inflorescence types. A key for the identification of these inflorescence types is presented. Generally, inflorescence characters have definite systematic value in recognizing supra-generic taxa in the Chloridoideae. Twelve processes have been identified as responsible for inflorescence diversification that awaits verification by further systematic study.     

Development of the epiphyllous inflorescence of Phyllonoma integerrima (Turcz.) Loes.: implications for comparative morphology*

The inflorescence primordium of Phyllonoma integerrima (Turcz.) Loes. is initiated on the adaxial side of the leaf primordium. At about the same time, a vegetative bud is formed at the base of the same leaf primordium. The vascular anatomy is the same in the fertile and sterile leaves, except that in the fertile leaf an inflorescence trace departs from the midvein of the leaf at the point where the inflorescence is inserted. Neither the inception nor the procambial supply of the inflorescence provide evidence of “congenital fusion”of inflorescence and leaf. It is also argued that the idea of an “adventitious”origin of the inflorescence is not useful in this case. Consequences for our conception of shoot construction are pointed out. It is argued that positional changes in the initiation of organs is an evolutionary process that may have remarkable effects on plant construction.     

孟仁草的花序发育研究

在光学显微镜和扫描电镜下观察了禾本科(Poaceae)虎尾草属(Chloris Sw.)孟仁草(Chloris barbata Sw.)的花序发育过程,以寻找适于虎尾草群(Chloris group)分支分析的发育性状.结果发现了未见于成熟花序的23个发育性状.阐明盂仁草花序的本质是二级长侧枝包围平截的主轴构成指形花序.该类型花序仅见于单子叶植物和少数高度特化的双子叶植物.涉及花序分枝的分子遗传机制研究亟待开展.     

Inflorescence diversity and evolution in the PCK Clade (Poaceae: Panicoideae: Paniceae)

The PCK Clade, represented by six to nine genera, is a monophyletic group situated within the Paniceae tribe. The highly diverse inflorescences within the PCK Clade provide an interesting system for the study of morphological evolution and also may aid in better understanding its unclear systematics. The inflorescence structure of 110 members of the PCK Clade has been investigated. Inflorescences are polytelic showing different levels of truncation. At least 21 different inflorescence subtypes were identified. Fourteen variable inflorescence characters were found, among which some have suprageneric or infrageneric value and others are polymorphic. A key for the identification of inflorescence types is presented. Nine processes have been identified as responsible for inflorescence diversification. Highly branched inflorescences with different internode lengths are present in the basal genus whereas truncated inflorescence morphologies appear late in the history of the clade. The precise timing of morphological changes is impossible to assess until we have a well supported phylogeny for the PCK Clade.     

不同水分条件刚毛柽柳开花结实观测

使用参照对比方法,观测了正常水分条件(参照点)与断流30年后输水河畔不同水分梯度刚毛柽柳(Tamarix hispida)单个花序长、单个花序开花数、单个花序结实量、单个花序结实率和种子发芽率的差别.结果表明:除结实率、发芽率外,参照点与输水河畔不同水分条件刚毛柽柳的各项观测指标均存在极显著差异;应急输水7年后,离河300 m,地下水埋深值5.5 m左右,刚毛柽柳可保证一定的花序长和开花数;离河500 m,地下水埋深值6 m左右,刚毛柽柳可保证一定结实量;离河1 000 m以内,地下水埋深＜7.5 m,刚毛柽柳种子的结实率和发芽率仍相对较高;干旱条件限制刚毛柽柳的花序长与开花数,随水分条件下降又限制其结实量;在缺水条件下,刚毛柽柳仍保证一定的结实率及发芽率以确保种群的延续.     

Inflorescence architecture affects pollinator behaviour and mating success in Spiranthes sinensis (Orchidaceae)

? Despite the wide inflorescence diversity among angiosperms, the effects of inflorescence architecture (three-dimensional flower arrangement) on pollinator behaviour and mating success have not been sufficiently studied in natural plant populations. ? Here, we investigated how inflorescence architecture affected inter- and intra-plant pollinator movements and consequent mating success in a field population of Spiranthes sinensis var. amoena (S. sinensis). In this species, the flowers are helically arranged around the stem, and the degree of twisting varies greatly among individuals. The large variation in inflorescence architecture in S. sinensis results from variation in a single structural parameter, the helical angle (the angular distance between neighbour-flower directions). ? The numbers of visits per inflorescence and successive probes per visit by leaf-cutting bees decreased with helical angle, indicating that individual flowers of tightly twisted inflorescences received less visitations. As expected from pollinator behaviour, pollinia removal and fruit set of individual flowers decreased with helical angle. Meanwhile, geitonogamy decreased in tightly twisted inflorescences. ? Our novel findings demonstrate that natural variation in inflorescence architecture significantly affects pollinator behaviour and reproductive success, suggesting that inflorescence architecture can evolve under pollinator-mediated natural selection in plant populations. We also discuss how diverse inflorescence architectures may have been maintained in S. sinensis populations.     

Inflorescence structure in Rhynchospora Vahl (Cyperaceae)

We investigated the inflorescence structure of Rhynchospora following the methodology and terminology of Troll's school, with the objective of providing a characterization of the inflorescence suitable to evaluate the processes responsible for the diversity observed. Homogenization of inflorescence structures may occur fully or partially. In the first case, all branches of the inflorescence are homogeneous, while in the later, distal and proximal parts of the inflorescence bear homogeneous branches, but in the middle portions of the inflorescence non-homogeneous branches exist. Other characters leading to different forms of inflorescences are branching degree, internode elongation along the main axis of the synflorescence, degree of epipodium elongation of distal paraclades, development of bract and prophyll, and development of prophyllar paraclades. We identified three main types of inflorescences: (1) partially homogeneous paniculodia, (2) partially homogeneous capitate heads, and (3) a fully homogeneous capitate head. Within the first type, four subtypes were also recognized. Finally, we discuss how these processes can operate to produce the variation of the inflorescence shape.     

An Inflorescence Disease of Amaranthus spp. in Nigeria Associated with Choanephora cucurbitarum

Abstract Symptoms of a devastating inflorescence disease of Amaranthus spp. associated with Choanephora cucurbitarum are described. It is characterized by extensive blighting of the inflorescence head and is often accompanied by inflorescence dieback and severe breaking of the floral head. In fields with severe infestation and under favourable conditions the inflorescence heads may be completely cut off. Such a plant will not produce any seeds or the yield may be reduced to half or less.
Laboratory experiments confirm observations made in the field that the fungus is aggressively pathogenic on the apical region of the inflorescence. Usually, the green young inflorescences are more susceptible.