Spatial pattern of ovule maturation in the inflorescence of Echium vulgare: demography, resource allocation and the constraints of architecture

Many of the flowers produeed bv a plant fail to mature seeds despite effective pollination. The role of inflorescence architecture governing patterns of abortion in plants has been underestimated. 1 he inflorescence of Echium vulgare L. comprises a raceme bearing lateral inflorescences, each of which is cymosc. Within each cyme, there is a correlation between the proximity of a flower to the main axis and its order of flowering; and (lie probability of it maturing seeds. These findings appear to result from a decrease in the availability of maternal resources as the flowering period progresses. No relationship could be shown between the position of the cyme on the main inflorescence and the number of seeds set per flower although position was correlated with the length of the cyme, the number of (lowers and the length of the subtending bract. The mctamcric units of E. vulgare appear to function largely independently in their assimilation of resources. Larger cymes not only bear more flowers, but also draw on a larger area of photosynthetic tissue for resources. This hypothesis is supported by the removal of the bract or of part of the cyme at the onset of flowering; cymes without bracts mature fewer ovules than controls while decapitated cymes mature a greater proportion of ovules.     

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.     

Pseudoracemes in papilionoid legumes: their nature, development, and variation

Pseudoracemes in papilionoid legumes: their nature, development, and variation. Cymelike partial inflorescences called fascicles have been reported in the inflorescences of several papilionoid tribes. The total inflorescence is termed a ‘pseudoraceme’ because of the multiple flowers in each bract axil. Pseudoraceme development has been studied in 22 taxa in five papilionoid tribes (Abreae, Desmodieae, Millcttieae, Phaseoleae and Psoraleeae). Two to twelve flowers occur per bract axil among various taxa, with three the most common number.Pongamia pinnata and Clitoris fairchildiana have only two flowers per axil; Vigna radiata, Phaseolus vulgaris, and Apios americana have four to five commonly, and Dioclea aff.ucayalina and Abrus precalorius have up to 12. The ‘fascicle’ usually consists of a triad of three flowers; each triad resembles a dichasial cyme in that the middle flower appears terminal. The middle flower however is subtended by a bract on the abaxial side, so that the middle flower is technically lateral. When the first-order axis elongates, each triad may either remain intact or be separated by axis intervalS. Many variations on the basic triad pattern occur in the species studied: 1.one or two flowers may develop while others that are initiated remain suppressed; 2. Additional flowers may be produced that replicate the first triad; 3. Additional flowers may form medianly only, on the abaxial side. The second-order inflorescence axis which has produced the three flowers persists to produce more flowers in replication of the triad pattern in several taxa (Apios americana, Vigna radiata, Phaseolus vulgaris, and Dioclea aff.ucayalina). In Butea monosperma the second-order inflorescence apex produces subsequent flowers (after the triad) in a helix. In Erylhrina perrieri, there is no indication of a persistent second-order inflorescence apex after the central flower; such a condition could be interpreted as a cyme, except for the abaxial subtending bract. The triad in Psoralea pinnata is a true cyme; the middle flower lacks a subtending bract other than that subtending the entire fascicle. Developmentally, the difference between a cyme and an early-determinate raceme (as in the triad type of pseudoraceme) is rather slight. Comparison of the types of inflorescences described here may indicate how the transition may have occurred between racemes and cymes in the evolution of legumes.     

Ontogeny of Tendrils in Antigonon leptopus H. & Arn.

In Antigonon leptopus the main tendrillar and axillary branchis a modified inflorescence axis. It usually bears 6–7lateral bracts out of which 3–4 lower ones are small andleaf-like while the upper 2–3 are tendrillar; 2–3tendrils are also present at its terminal end. The vegetativeshoot apex shows a single layer of tunica and an inner massof corpus without any cytohistological zonation. The earliestaxillary bud or tendril meristem arises at the second node andit elongates due to rib meristem activity. The bract primordiaarise in an acropetal succession. The initiation of the bract-tendriland the leafy bract is similar. In the development of the bract-tendril,marginal meristem activity is absent or reduced and the differentiationof the apical and subapical initials is absent. The terminalbract-tendrils arise as lateral appendages and the residuumof the apical meristem of the main axillary tendril persistsfor some time. In the flowering period the floral buds arisein the axils of the bracts and bract-tendrils. No flowers arepresent in the axils of terminal bract-tendrils.     

铁破锣花序的开花特性与昆虫传粉的相互关系研究

为了揭示植物花的空间布局与开花动态的调节机制以及避免同株异花传粉的生态学策略,该研究对铁破锣［Beesia calthifolia (Maxim.) Ulbr.］花序形态结构、开花动态和传粉生物学进行了观察分析。结果表明：（1）铁破锣花序结构设计巧妙,由3朵花组成一个聚伞花序单元并依次排列在主花序轴上,且花序轴上聚伞花序之间距离较远。（2）铁破锣通过单个聚伞花序顶花先开,通常只有6～8朵聚伞花序的顶花同时开放,而且总状花序从基部到顶部逐次开放,从而使得大量聚集单花的花序达到尽量少开花。（3）铁破锣花白色,花粉是访花昆虫的仅有诱物,纤细巴蚜蝇（Baccha maculata）是铁破锣的主要传粉昆虫,这种昆虫能够以花丝为着力点取食花粉,通常在一个花序上取食一朵单花后很快飞向另外一个花序的花。研究认为,铁破锣花序的空间设计和开花的时间序列动态减少了昆虫访问同株异花的可能性。     

Density Studies on Lupins: I. Flower Development

In an August-sown experiment the pattern of flower developmentwas followed for cv. Ultra (Lupinus albus L.) and cv. Unicrop(L. angustifolius L.) grown at low (10 plants m^–2) andhigh (93 and 83 plants m^–2, Ultra and Unicrop respectively)densities. Dry weight increase of flowers on the main-stem inflorescenceand first lateral below the main-stem were compared at differentfloral stages. Maximum flower weight was reached just priorto the open flower stage and remained constant or declined untila pod formed or abscission occurred. The time period betweenmaximum flower weight and pod formation or abscission was upto 10 days. Emergence of the inflorescence was earlier and thefirst flower of Ultra opened 10 days before Unicrop. Developmentof each terminal raceme (inflorescence) was acropetal, withpods having formed on lower flower nodes when terminal flowerswere still quite immature. Laterals forming the next generationof inflorescences grew from axillary leaf buds below an inflorescencewhile it was in full flower. Sources of competition from connectedreproductive and vegetative metabolic sinks are discussed. Lupinus spp., lupins, flower development, planting density     

千金榆花序及花器官发育

在扫描电镜下首次观察了桦木科鹅耳枥属千金榆花序和花的形态发生过程。千金榆雌花序由多个小聚伞花序螺旋状排列组成;每个小花序原基分化出1枚初级苞片和一团小花序原基分生组织,由小花序原基分生组织分化形成2个花原基和2个次级苞片;每个花原基分化出2个心皮原基,形成1个二心皮雌蕊;次级苞片远轴面发育快于近轴面,呈不均等的联合状;雌蕊基部有1层环状花被原基。雄花序为柔荑状,由多个小聚伞花序螺旋状排列组成;每个小花序原基分化出1枚初级苞片和一团小花序原基分生组织,由小花序原基分生组织分化出3个花原基分区,并分化形成3朵小花,小花无花被,位于两侧的小花分别有2枚雄蕊,位于中央的小花有4枚雄蕊,雄蕊共8枚,稀为10枚,该3朵小花为二歧聚伞状排列,其花基数应为2基数。     

Pair-flowered cymes in the Lamiales: structure,distribution and origin

Background and Aims

In the Lamiales, indeterminate thyrses (made up of axillary cymes) represent a significant inflorescence type. However, it has been largely overlooked that there occur two types of cymes: (1) ordinary cymes, and (2) ‘pair-flowered cymes’ (PFCs), with a flower pair (terminal and front flower) topping each cyme unit. PFCs are unique to the Lamiales and their distribution, origin and phylogeny are not well understood.

Methods

The Lamiales are screened as to the occurrence of PFCs, ordinary cymes and single flowers (constituting racemic inflorescences).

Key Results

PFCs are shown to exhibit a considerable morphological and developmental diversity and are documented to occur in four neighbouring taxa of Lamiales: Calceolariaceae, Sanango, Gesneriaceae and Plantaginaceae. They are omnipresent in the Calceolariaceae and almost so in the Gesneriaceae. In the Plantaginaceae, PFCs are restricted to the small sister tribes Russelieae and Cheloneae (while the large remainder has single flowers in the leaf/bract axils; ordinary cymes do not occur). Regarding the origin of PFCs, the inflorescences of the genus Peltanthera (unplaced as to family; sister to Calceolariaceae, Sanango and Gesneriaceae in most molecular phylogenies) support the idea that PFCs have originated from paniculate systems, with the front-flowers representing remnant flowers.

Conclusions

From the exclusive occurrence of PFCs in the Lamiales and the proximity of the respective taxa in molecular phylogenies it may be expected that PFCs have originated once, representing a synapomorphy for this group of taxa and fading out within the Plantaginaceae. However, molecular evidence is ambiguous. Depending on the position of Peltanthera (depending in turn on the kind and number of genes and taxa analysed) a single, a double (the most probable scenario) or a triple origin appears conceivable.     

Distribution patterns of hummingbird flower mites (Gamasida: Ascidae) in relation to floral availability on Heliconia inflorescences

I analyzed the dispersion patterns of ascid mites (Gamasida:Ascidae) on inflorescences of Heliconia trinidatis in relationto the temporal and spatial distribution of open flowers. Openflowers last only a few hours and are the locations of foodas well as the sole sites from which mites disperse on visitinghummingbirds. All inflorescences were inhabited by populationsof nectarivorous Rhinoseius trinitatis and omnivorous Lasioseiuselegants. All demographic groups of R. trinitatis were associatedstrongly with bracts bearing open flowers on the day of inflorescencecollection or with bracts that would have had an open floweron the day after collection. For L. elegans, only larval distributioncoincided with open flowers. Laboratory observations demonstratedthat mites move throughout an inflorescence at night and preferentiallyaggregate where the next flower will open. Mites enter flowersimmediately at, or just before, anthesis, and unerringly exitopen flowers well in advance of floral abscission. Hummingbirdflower mites exhibit a variety of behavioral adaptations, indicatingextraordinary sensitivity to the physiological and biochemicalnuances of their host inflorescences.     

Branch length mediates flower production and inflorescence architecture of Fouquieria splendens (ocotillo)

The capacity of individual branches to store water and fix carbon can have profound effects on inflorescence size and architecture, thus on floral display, pollination, and fecundity. Mixed regression was used to investigate the relation between branch length, a proxy for plant resources, and floral display of Fouquieria splendens (ocotillo), a woody, candelabraform shrub of wide distribution in arid North America. Long branches produced three times as many flowers as short branches, regardless of overall plant size. Long branches also had more complex panicles with more cymes and cyme types than short branches; thus, branch length also influenced inflorescence architecture. Within panicles, increasing the number of cymes by one unit added about two flowers, whereas increasing the number of cyme types by one unit added about 21 flowers. Because flower production is mediated by branch length, and because most plants have branches of various lengths, the floral display of individual plants necessarily encompasses a wide range of inflorescence size and structure.     

NEW INTERPRETATION OF THE INFLORESCENCE OF FAGUS DRAWN FROM THE DEVELOPMENTAL STUDY OF FAGUS CRENATA,WITH DESCRIPTION OF AN EXTREMELY MONSTROUS CUPULE

The inflorescence of Fagus is generally considered to be a determinate one, i.e., an axillary dichasium, in contrast to those of most genera in the family, which are indeterminate, dichasial, or simple catkins. To understand the relationship between the two types, ontogenetic development of the inflorescence of Fagus crenata was investigated. The early developmental stages are similar in both the male and the female inflorescences. At first, the inflorescence is oval-shaped, then a swelling forms at the distal side of it. Subsequently, another swelling forms at the proximal side. The more or less conspicuous residual part of the primary inflorescence axis remains between the two swellings. The inflorescence becomes heart-shaped and the first flower forms at the summit of each swelling. Subsequently, higher-ordered flowers form dichasially in the male inflorescence, and the cupule valves differentiate in the female one. This organogenetic manner suggests that the inflorescence of Fagus is an indeterminate one, consisting of two dichasia arranged alternately on the primary axis. The scale leaves surrounding the inflorescence were also given a new interpretation. They were considered to be stipules of the bracts, because sometimes they constitute a continuous structure, together with an inconspicuous swelling between them. A proliferous-type monstrous cupule was interpreted as supporting evidence for the hypothesis.     

Morphological correlates of nectar production used by honeybees

Abstract.  1. Honeybees foraging on lavender have been shown to choose inflorescences that are larger and have more flowers. If they are selecting optimally then these inflorescences should yield higher net rates of energy gain. The number and distribution of flowers within inflorescences is a complex function of age, however, which might itself influence nectar quality and availability.
2. Sampling of the overnight nectar secretion of visited and unvisited inflorescences showed that younger inflorescences with more flowers produced more sugar per flower and had fewer unproductive flowers than other inflorescences, but the size of the inflorescence had no effects.
3. Overall display size attracted bees to inspect inflorescences, as inflorescences that were inspected but rejected were larger and/or had larger or more bracts than those that were ignored. Bees, however, accepted more productive inflorescences based on different cues: inflorescence age and number of flowers.
4. Inflorescence choice thus appeared to reflect a two-stage decision process based on different morphological criteria at each stage.     

外来物种黄顶菊花器官分化的初步研究

利用扫描电镜(SEM)观察了黄顶菊(Flaveria bidentis(L.)Kuntz)花序发育过程中蝎尾状聚伞花序、头状花序和小花的形成.黄顶菊的花序由主轴及一至三级分枝组成,各级分枝交互对生,形成方式相同.植株主轴和侧枝顶端的每个花序由3～6个蝎尾状聚伞花序密集而成;每一蝎尾状聚伞花序由5～15个头状花序组成;每一头状花序中有4～11枚小花.小花分化顺序为5个花冠原基、5个雄蕊原基和2个心皮原基.2007年,天津地区黄顶菊的花期是7月下旬到9月下旬.7月中旬,花序和花器官原基不断形成并分化,至花器官成熟经历的时间约15 d.     

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     

Development and morphology of flowers and inflorescences in Balanophora papuana and B. elongata (Balanophoraceae)

Extreme modification and reduction in floral morphology presents an obstacle to determining the evolutionary relationships and homologies of the holoparasites in Balanophoraceae. Developing flowers and inflorescences of two dioecious species, Balanophora papuana and B. elongata, were compared to each other and to the monoecious B. fungosa. Intermingled with flowers in the male inflorescences are bracts (B. elongata) or bract parts (B. papuana). In the latter, early cessation of bract tip growth results in two half-bracts, which become displaced during inflorescence elongation, thus disproving the view that these bract-like structures are axial in nature. Male flower primordia emerge in positions axillary to the dividing bracts, and both arise in a spiral sequence. This pattern is modified in B. papuana by the formation of pseudowhorls of four. In both species, the staminate flowers consist of a generally four-merous perianth and a synandrium of congenitally fused stamens. Male flower and bract ontogeny (but not pollen sacs) conform to patterns seen in other angiosperms. More problematic are the carpellate flowers whose primordia arise in irregular order between club-shaped, radially symmetrical organs called claviform bodies. The interpretation that these bodies are homologous to the peltate bracts of Helosideae appears plausible, but cannot explain their nonspiral initiation and radial symmetry.     

Wo new species of Viscum (Viscaceae) from China

Two new species of Viscum from the southern and southwestern China are described and illustrated. Both Viscum macrofalcatum and V. hainanense are monoecious plants with inflorescences axillary, usually 3–5 flowers in one cyme, the middle one male, outer ones females. Viscum macrofalcatum differs from V. hainanense by having 1–6 sessile cymes in the axil, whereas V. hainanense has only 1 cyme in the axil, and peduncle 0.5–1 mm long. The most closely related species to these entities is V yunnnanense. Based on the habit and habitat, external morphology, and palynological characters, we concluded that the three entities are specifically distinct.     

Quantitative developmental analysis of homeotic changes in the inflorescence of Philodendron (Araceae)

Background and Aims: The inflorescence of Philodendron constitutes an interestingmorphological model to analyse the phenomenon of homeosis quantitativelyat the floral level. The specific goals of this study were (1)to characterize and quantify the range of homeotic transformationin Philodendron billietiae, and (2) to test the hypothesis thatthe nature of flowers surrounding atypical bisexual flowers(ABFs) channel the morphological potentialities of atypicalbisexual flowers. Methods: Inflorescences of P. billietiae at different stages of developmentwere observed using SEM. The number of appendices in male, femaleand sterile flowers were counted on 11 young inflorescences(5–6 flowers per inflorescence). The number of staminodesand carpels on ABFs were counted on 19 inflorescences (n = 143).These data were used for regression and ANOVA analyses. Results: There was an average of 4·1 stamens per male flower,9·8 carpels per female flower and 6·8 staminodesper sterile male flower. There was an average of 7·3floral appendices per atypical flower. Staminodes and carpelsare inserted on the same whorl in ABFs. A negative exponentialrelationship was found between the average number of staminodesand the number of carpels in ABFs. If only the ABFs consistingof less than six carpels are considered, there is a linear relationshipbetween the number of carpels and the average number of staminodes.The value of the slope of the regression equation indicatesthat on average, in P. billietiae, 1·36 carpels are replacedby one staminode. Conclusions: In P. billietiae, the number of appendages in female flowersimposes a constraint on the maximum total number of appendages(carpels and staminodes) that can develop on ABFs. The quantitativeanalyses indicate that the average number of different typesof floral appendages on an ABF and the number of organs involvedin a homeotic transformation are two independent phenomena.     

Morphology and Anatomy of Stems and Pedicels of Spring Flush Shoots Associated with Citrus Fruit Set

Flowering and vegetative shoots of ‘Shamouti’ orange[Citrus sinensis (L.) Osbeck] and ‘Marsh’ seedlessgrapefruit (Citrus paradisi Macf.) were examined for correlationof their morphology and anatomy with fruit set. Fruit set isfavoured on leafy inflorescences whereas abortion is nearlycomplete on leafless inflorescences. Leafless inflorescencesof ‘Shamouti’ with one flower were found to havea very thin stem which contained few vascular bundles, whereasthose with three flowers had better-developed vascular systems.The vascular system of leafy inflorescences is significantlydifferent from that of leafless ones and contains a distinctcentral xylem cylinder. The vascular area of leafless inflorescencesis only about one-quarter of that of the leafy ones. The vascularsystem of grapefruit resembles that of the ‘Shamouti’orange. This study emphasizes the importance of the dimensionof the vascular system for fruit set and provides a possibleexplanation for the better fruit set on both leafy and leaflessinflorescences with several flowers compared with single-floweredinflorescences. Anatomy; citrus; fruit set; leafless inflorescence; leafy inflorescence; pedicel; vascular system; vegetative shoot     

THE MORPHOLOGY AND RELATIONSHIPS OF DALECHAMPIA SCANDENS (EUPHORBIACEAE)

The circumtropical but preponderantly American genus Dalechampia, comprising nearly 100 species of twining vines (or rarely subshrubs), is strikingly isolated within the Euphorbiaceae because of its distinctive bibracteate inflorescences. There has been considerable taxonomic controversy with regard to the relationships of the genus, and it has been suggested that Dalechampia is allied to the tribe Euphorbieae because of a supposed analogy between its inflorescence and the cyathium in the Euphorbieae. Field and laboratory investigations of the common American species D. scandens, together with a comparative survey of related species, have thrown some light on these problems. The Dalechampia inflorescence seems best interpreted as consisting of a terminal staminate pleiochasium (with part of the lateral branches transformed for nectar production), juxtaposed to a 3-flowered pistillate cyme. The lips of the conspicuous bilabiate involucre are formed by the hypertrophied bracts which subtend the staminate and pistillate cymes. The bisexual inflorescences appear to be distinctly proterogynous, rather than proterandrous, as has been previously suggested. The configuration of the inflorescence—a bilaterally symmetrical pseudanthium—suggests adaptation for crosspollination, but the closing movement of the bracts makes self-pollination probable in the absence of visits by pollinators. The similarity of the Dalechampia inflorescence to the cyathium of the Euphorbieae appears to be entirely superficial, and both reproductive and vegetative data suggest that Dalechampia is related to taxa of tribe Plukenetieae.     

THE ALLIUM INFLORESCENCE: SOME SPECIES OF THE SECTION MOLIUM

Mann , Louis K. (U. California, Davis.) The Allium inflorescence: some species of the section Molium. Amer. Jour. Bot. 46(10): 730–739. Illus. 1959.—The inflorescence is described for Allium neapolitanum, A. roseum, A. hirsutum, A. subhirsutum, A. zebdanense and A. erdelii, species of Molium, a Mediterranean section of the genus. Inflorescence structure is similar among these 6 species. The single spathe appears to consist of 4 coalesced bracts, each of which bears in its axil a bostryx (helicoid cyme) of 3–7 flowers. Central to these 4 peripheral bostryxes are several smaller ones which differentiate later and decrease in flower number toward the inflorescence center. Bracts and bracteoles (prophylls) are generally absent within the spathe. The inflorescence is not radially symmetrical and the bostryx on the side opposite the uppermost foliage leaf differentiates and develops first. Among the peripheral bostryxes there is a definite sequence of development and certain regularities of coiling (clockwise vs. counterclockwise). Within each bostryx the flowers open in a strict sequence from oldest to youngest; among the bostryxes, the 4 peripheral ones flower first, usually starting with the first bostryx to be differentiated. The central bostryxes flower last.