Flower variation and breeding systems in theCistaceae

Fourteen common southern Spanish species in theCistaceae were examined for quantitative variations in floral traits. These included the diameter of the corolla, number and size of anthers, number of ovules, and the size and shape of the gynoecium. The variables were in most instances positively correlated, species with larger flowers having more and larger anthers, more ovules, etc. Shrubs were observed to possess the largest, annuals the smallest, and subshrubs medium-sized flowers. Detailed observations of flower structure and function in a shrub (Cistus salvifolius), a spring-annual (Tuberaria guttata) and a winter-annual (T. inconspicua), revealed substantial variations in the breeding system. WhileC. salvifolius (and probably most woody species in this family) presents self-incompatibility, annual species ofTuberaria are self-compatible. In the studied population,T. inconspicua plants bore only reduced, cleistogamous flowers with no sign of a corolla.T. guttata has chasmogamous flowers that can facultatively self-pollinate.     

Comparative floral structure and systematics in Crossosomatales (Crossosomataceae, Stachyuraceae, Staphyleaceae, Aphloiaceae, Geissolomataceae, Ixerbaceae, Strasburgeriaceae)

Floral structure of all putative families of Crossosomatales as suggested by molecular studies was comparatively studied. The seven comprise Crossosomataceae, Stachyuraceae, Staphyleaceae, Aphloiaceae, Geissolomataceae, Ixerbaceae, and Strasburgeriaceae. The entire clade (1) is highly supported by floral structure, also the clades (in sequence of diminishing structural support): Ixerbaceae/Strasburgeriaceae (2), Geissolomataceae/Ixerbaceae/Strasburgeriaceae (3), Aphloiaceae/Geissolomataceae/Ixerbaceae/Strasburgeriaceae (4), and Crossosomataceae/Stachyuraceae/Staphyleaceae (5). Among the prominent floral features of Crossosomatales (1) are solitary flowers, presence of a floral cup, imbricate sepals with outermost smaller than inner, pollen grains with horizontally extended endoapertures, shortly stalked gynoecium, postgenitally united carpel tips forming a compitum, stigmatic papillae two‐ or more‐cellular, ovary locules tapering upwards, long integuments forming zigzag micropyles, cell clusters with bundles of long yellow crystals, mucilage cells, seeds with smooth, sclerified testa and without a differentiated tegmen. Clade (2) is characterized by large flowers, petals forming a tight, pointed cone in bud, stamens with long, stout filaments and sagittate anthers, streamlined, conical gynoecium, antitropous ovules, rudimentary aril, lignified, unicellular, T‐shaped hairs and idioblasts with striate mucilaginous cell walls. Clade (3) is characterized by alternisepalous carpels, punctiform stigma formed by postgenitally united and twisted carpel tips, synascidiate ovary, only one or two pendant ovules per carpel, nectary recesses between androecium and gynoecium. Clade (4) is characterized by pronounced ‘pollen buds’. Clade (5) is characterized by polygamous or functionally unisexual flowers, x‐shaped anthers, free and follicular carpels (not in Stachyuraceae). Crossosomataceae and Aphloiaceae, although not retrieved as a clade in molecular studies, share several special floral features: polystemonous androecium; basifixed anthers without a connective protrusion; stigma with two more or less decurrent crests; camplyotropous ovules and reniform seeds; simple, disc‐shaped nectaries and absence of hairs. © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society, 2005, 147 , 1–46.     

A perfect flower from the Jurassic of China

Flower, enclosed ovule and tetrasporangiate anther are three major characters distinguishing angiosperms from other seed plants. Morphologically, typical flowers are characterised by an organisation with gynoecium and androecium surrounded by corolla and calyx. Theoretically, flowers are derived from their counterparts in ancient ancestral gymnosperms. However, as for when, how and from which groups, there is no consensus among botanists yet. Although angiosperm-like pollen and angiosperms have been claimed in the Triassic and Jurassic, typical flowers with the aforesaid three key characters are still missing in the pre-Cretaceous age, making many interpretations of flower evolution tentative. Thus searching for flower in the pre-Cretaceous has been a tantalising task for palaeobotanists for a long time. Here, we report a typical flower, Euanthus paniigen. et sp. nov., from the Middle–Late Jurassic of Liaoning, China. Euanthus has sepals, petals, androecium with tetrasporangiate dithecate anthers and gynoecium with enclosed ovules, organised just like in perfect flowers of extant angiosperms. The discovery of Euanthus implies that typical angiosperm flowers have already been in place in the Jurassic, and provides a new insight unavailable otherwise for the evolution of flowers.     

Transference of function in the pollination system of theOchnaceae

Most members of theOchnaceae possess poricidal anthers that are emptied by pollen collecting bees performing vibrational foraging. In several genera, such asTyleria, Adenarake, and various species ofSauvagesia, however, pollen is released by vibration from the anthers through the porus of a novel structure formed by staminodia. These envelop the androecium and gynoecium. Anthers enclosed in this envelope are often longicidal.     

Evolutionary trends in the androecium of theOrchidaceae

The evolution of the androecium in theOrchidaceae shows three major trends. There is a progressive trend in the degree of fusion of the filament(s) and staminode(s) to the gynoecium. Secondly, there is a reduction in the number of fertile anthers. Finally, there is a progressive change in the position of the base of the anther relative to the apex of the stigma; in the more primitive orchids the apex of the stigma is always higher than the base of the anther (this position is reversed in the higher orchids). All three trends reflect variation in the evolution of pollen dispersal and pollen reception mechanisms in theOrchidaceae. Trends in the evolution of the orchid anther(s) tend to parallel trends in the evolution of their pollinaria.     

Floral ontogeny of Knema and Horsfieldia (Myristicaceae): evidence for a complex androecial evolution

The floral ontogeny of two species of Knema and one of Horsfieldia was examined and described using scanning electron microscopy. The perianth is trimerous with three tepals arising in succession. Pistillate flowers have a rounded floral apex with a convex top. The single carpel primordium is initiated along the margin of the bud and develops a plicate shape with an apical bilobed stigma. In staminate flowers, the floral apex is broadly hemispherical with a somewhat three‐sided shape. Several anther primordia are initiated almost simultaneously around the margin of the floral apex. In Horsfieldia, stamens extend laterally in antetepalous groups, whereas, in Knema, anthers form two whorls. The alternitepalous stamens were found to be different from the antetepalous stamens, which are pressed within a limited space. The anther primordia remain adnate to the receptacle and grow longitudinally, producing a pair of microsporangia. The central area of the floral apex persists as an undifferentiated residuum without any trace of a gynoecium. Myristicaceous anthers are basically homologous, although the number of anthers, pollen sacs and shape of the androecium are variable. The evolution of the androecium is discussed in the family, with opposing possibilities for reductions and increases in anther number in Myristicaceae. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 164 , 42–52.     

弯齿盾果草(紫草科)花序及花的形态发生

以弯齿盾果草不同发育时期的花芽为材料,在体视显微镜解剖观察的基础上使用扫描电镜对弯齿盾果草花序、花及果实的发育过程进行了观察。结果显示:(1)弯齿盾果草的花序是由最初的一个球形花序原基经过多次分裂形成的,且花序发生式样符合蝎尾状聚伞花序结构,而非通常所描述的镰状或螺状聚伞花序;花序发生过程中无单一主轴,花序轴是由侧枝连接而成,每一朵花原基有其对应的1枚苞片,下一花原基是从相邻的上一枚苞腋里发生,相邻两花原基交错互生。(2)花器官的发生是按照花萼原基、花冠原基、雄蕊原基和雌蕊原基的顺序发育,但雄蕊原基的花药部分发育速度要比花冠原基快,所以花器官的发育是按照花萼、雄蕊、花冠和雌蕊的顺序发育。(3)子房四深裂结构是由4个原基分别发育,而后相互靠拢而成。(4)小坚果表面的附属结构发生于子房发育后期,其背面的内外层突起分别是由生长较快的外部组织的边缘通过上部内缩和下部向外环状生长形成。     

FUNCTIONAL DIOECY AND ANDROMONOECY IN SOLANUM

Field and laboratory studies of 19 diclinous species endemic to Australia help to clarify the nature and evolution of andromonoecy, androdioecy, and dioecy in the genus Solanum. Ten species are andromonoecious; typically these species bear inflorescences with a single, large basal hermaphroditic flower and 12–60 distal, smaller staminate flowers. We suggest that the andromonoecious condition was derived from hermaphroditic-flowered ancestors in part by hemisterilization of flowers but largely by addition of staminate flowers. The resultant larger inflorescences are hypothesized to serve both to attract and to entrain pollinators, yielding more or higher-quality seed set in hermaphroditic flowers and/or greater dispersion of pollen from staminate flowers. We suggest that andromonoecy may also serve to reduce selling. Nine other species are morphologically androdioecious but functionally dioecious. In these species, staminate flowers, like those of the andromonoecious species, bear anthers with copious tricolporate pollen and a highly reduced gynoecium. The morphologically hermaphroditic flowers are functionally pistillate and borne singly in inflorescences, and they bear anthers with inaperturate pollen. The inaperturate pollen, although viable, never germinates and is hypothesized to be retained in pistillate flowers as a reward to pollinators in the nectarless Solanum flowers. All other species of Solanum studied with pollen dimorphism in which one pollen morph is inaperturate are also best treated as functionally dioecious. We conclude that there is no evidence for androdioecy in Solanum. A review of other families suggests that there is little support for this unusual breeding system in any other angiosperm group either. Preliminary analyses suggest that andromonoecy and dioecy are polyphyletic in Solanum. Furthermore, dioecy is as likely to have arisen from hermaphroditic as from andromonoecious ancestors.     

Floral development in Anemoneae (Ranunculaceae)

The floral development of two Clematis species and four Anemone species (including Pulsatilla) (Anemoneae, Ranunculaceae) is described. Shared features are: (1) sepals shortly after initiation broad, crescent‐shaped, as opposed to the other organs, which are narrow and hemispherical; (2) outermost organs of the androecium often smaller than the others and sometimes sterile; (3) carpels ascidiate, with distinctive stalk, stigma papillate, decurrent; the carpels have one median fertile ovule and a few lateral sterile ovules in all species studied; the fertile ovule appears before the carpel closes. Generic differences are: (1) In Clematis, four sepals are initiated in two pairs; sometimes one of the sepals in the second pair appears to be divided into two organs (double position) resulting in a pentamerous perianth; the first eight stamens are positioned in two alternating whorls, the outer whorl alternating with the four sepals. In Anemone, the perianth organs, if five, are initiated in spiral sequence; in the Pulsatilla group of Anemone, six sepals are initiated in two whorls; the first three organs of the androecium (staminodes) alternate with the inner sepals. (2) Further androecial organs are mostly in complex whorls (i.e. including double positions) in Clematis, but in an irregular spiral or in irregular complex whorls in Anemone. (3) Anther maturation is largely centripetal in Clematis, but centrifugal or bidirectional in Anemone. In Clematis macropetala, the outermost organs of the androecium lack anthers and the filaments expand and become petal‐like. In contrast, in the Pulsatilla group of Anemone, these organs retain sterile anthers and become small, capitate organs. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 162 , 77–100.     

Floral structure and relationships ofHortonia (Monimiaceae)

The flowers ofHortonia angustifolia were investigated for their phyllotaxis, morphology, anatomy and development of the perianth, androecium and gynoecium. Certain features were also studied inH. ovalifolia. Characters so far overlooked further support the isolated and intermediate position of the genus between theAtherospermataceae andMonimiaceae s. str. and its archaic position among theLaurales. Dedicated to Professor Dr.W. Leinfellner on the occasion of his 70th birthday.     

Comparative floral anatomy and ontogeny in Magnoliaceae

Floral anatomy and ontogeny are described in six species of Magnoliaceae, representing the two subfamilies Liriodendroideae (Liriodendron chinese and L. tulipifera) and Magnolioideae, including species with terminal flowers (Magnolia championi, M. delavayi, M. grandiflora, M. paenetalauma) and axillary flowers (Michelia crassipes). The sequence of initiation of floral organs is from proximal to distal. The three distinct outermost organs are initiated in sequence, but ultimately form a single whorl; thus their ontogeny is consistent with a tepal interpretation. Tepals are initiated in whorls, and the stamens and carpels are spirally arranged, though the androecium shows some intermediacy between a spiral and whorled arrangement. Carpels are entirely free from each other both at primordial stages and maturity. Ventral closure of the style ranges from open in Magnolia species examined to partially closed in Michelia crassipes and completely closed in Liriodendron, resulting in a reduced stigma surface. Thick-walled cells and tannins are present in all species except Michelia crassipes. Oil cells are normally present. Floral structure is relatively homogeneous in this family, although Liriodendron differs from other Magnoliaceae in that the carpels are entirely closed at maturity, resulting in a relatively small stigma, in contrast to the elongate stigma of most species of Magnolia. The flower of Magnolia does not terminate in an organ or organ whorl but achieves determinacy by gradual diminution.     

THE MORPHOLOGY OF THE MYRISTICACEAE. I. FLOWERS OF MYRISTICA FRAGRANS AND M. MALABARICA

Floral histology and vascular anatomy of Myristica fragrans Van Houtt. and M. malabarica Lam. have been investigated from serial sections and specimens cleared in chloro-lacto-phenol. The flowers are unisexual. The androecium is considered to consist of a whorl of laterally concrescent anthers. The bisporangiate anthers are attached by a ridge of tissue to the terminal part of the androphore. In many cases the number of vascular bundles in the androphore is half the number of anthers. The gynoecium consists of a monocarpellate pistil with basal placentation and a single anatropous ovule. Of the many vascular bundles that enter the base of the carpel, two, because of their position and because they provide vascular traces to the ovule, are designated as ventral bundles. Additional ovular traces are provided by the carpel wall vascular system. These additional traces originate at the top of the locule and descend to the ovule. The similarity between the androecia of these two species and the androecium of the ćnellaceae is noted.     

Corolla wilting facilitates delayed autonomous self-pollination in Pedicularis dunniana (Orobanchaceae)

Structural changes associated with corolla wilting may serve as a mechanism for effecting self-pollination. Low pollinator visitation, high seed production and a corolla that persists after anthesis indicates that Pedicularis dunniana is autogamous. Delayed autonomous self-pollination is facilitated by corolla wilting. Wilting of the upper lip (galea) brought the pollen laden anthers into contact with the stigma resulting in the deposition of self pollen on the stigma. The seed set of flowers either emasculated, or with restrained galeae thus preventing anthers brushing against the stigma, was significantly lower than that of open-pollinated flowers. This demonstrates that autogamy occurs in this species through corolla wilting. Germination experiments indicated that outcross seedlings were more vigorous than selfed seedlings as a result of inbreeding depression. It is likely that autogamy provides reproductive assurance for P. dunniana under conditions of pollinator scarcity.     

Bee-pollination inHibbertia fasciculata (Dilleniaceae)

In direct contrast to mostHibbertia spp., the flowers ofH. fasciculata R. Br. ex D. C. bear only a single whorl of stamens and these stamens are arranged separately (not in typical bundles). The short filaments are appressed to the three carpels so that the inflated, porose and introrsive anthers form a centralized cluster obscuring the three ovaries. The three slender styles emerge at right angles from between the filaments. These styles curve upward and the stigmas form the three points of a triangle; each stigma is approximately one millimeter outside the centralized cluster of anthers. The flowers are nectarless and bear a bright yellow corolla. A pungent and unpleasant fragrance appears to be concentrated within the pollenkitt. When native bees attempt to forage for the pollen, within the cluster of anthers, the ventrally deposited loads of pollen, on the bees' abdomens, contact the outer triangle of stigmas. The major pollinators ofH. fasciculata are female bees in the polylectic genera,Lasioglossum (subgenusChilalictus, Halictidae) andLeioproctus (Colletidae). These bees carry an average of more than two pollen taxa when they are caught foraging onH. fasciculata. 78% of the 47 bees, captured onH. fasciculata carried the pollen from at least one sympatric taxon bearing nectariferous flowers (e.g., genera in theMyrtaceae, Compositae, andEpacridaceae). The pollination biology ofH. fasciculata is assessed in relation to the known radiation of bee-pollinated flowers in the genusHibbertia, and within theDilleniaceae s. l.     

Floral structure and evolution of primitive angiosperms: Recent advances

Concepts of primitive angiosperm flowers have changed in recent years due to new studies on relic archaic groups, new paleobotanical finds and the addition of molecular biological techniques to the study of angiosperm systematics and evolution.Magnoliidae are still the hot group, but emphasis is now on small primitive flowers with few organs and also on the great lability of organ number. Of the extant groups, a potential basal position of the paleoherbs has been discussed by some authors. Although some paleoherbs have a simple gynoecium with a single orthotropous ovule, anatropous ovules may still be seen as plesiomorphic in angiosperms. Anatropy is not necessarily a consequence of the advent of closed carpels. It may also exhibit biological advantages under other circumstances as is the case in podocarps among gymnosperms. Valvate anthers have now been found in most larger subgroups of theMagnoliidae (recently also in paleoherbs) and in some Cretaceous fossils. Nevertheless, as seen from its systematic distribution, valvate dehiscence is not necessarily plesiomorphic for the angiosperms, but may be a facultative by-product of the thick connectives and comparatively undifferentiated anther shape inMagnoliidae and lowerHamamelididae. A perianth is relatively simple in extantMagnoliidae or even wanting in some families. In groups with naked flowers the perianth may have been easily lost because integration in the floral architecture was less pronounced than in more advanced angiosperm groups. Problems with the comparison of paleoherb flowers with those ofGnetales are discussed. The rapid growth of information from paleobotany and molecular systematics requires an especially open attitude towards the evaluation of various hypotheses on early flower evolution in the coming years.     

Taxonomic revision of the genus Heliotropium (Boraginaceae s.l.) in south Yemen

The flora and fauna of Arabia, particularly southern Yemen, has recently attracted the interest of many authors. In this study, the genus Heliotropium L. (Boraginaceae) is taxonomically revised in southern Yemen. Ten species are recognized. Nomenclature, typification, representative specimens and a diagnostic key to all species are provided, along with their distribution in southern Yemen. The taxonomically most valuable characters in the genus are those of flowers (calyx, corolla, androecium and gynoecium) and nutlets, and those characters are thoroughly investigated and discussed. Both light and scanning microscopy are used in the investigation. Papillate anther apices (brush‐like) were recognized in some species. Connate anthers and deep or shallow ventral circular depressions on the nutlets were found to be useful in distinguishing members of H. sect. Orthostachys (viz. H. strigosum, H. rariflorum and H. ovalifolium), while winged nutlets were found only in H. pterocarpum. The length and hairiness of the style and stigma also proved to be taxonomically useful.     

In the right place at the right time: Parnassia resolves the herkogamy dilemma by accurate repositioning of stamens and stigmas

Background and Aims

Spatial (herkogamy) and temporal (dichogamy) separation of pollen presentation and stigma receptivity have been interpreted as reducing interference between male and female functions in hermaphroditic flowers. However, spatial separation leads to a potential conflict: reduced pollination accuracy, where pollen may be placed in a location on the pollinator different from the point of stigma contact.

Methods

To understand better how herkogamous flowers resolve this conflict, a study was made of a subalpine herb, Parnassia epunctulata, the nectariferous flowers of which exhibit sequential anther dehiscence (staggered pollen presentation) and stamen movements; usually one newly dehisced anther is positioned each day over the central gynoecium, while the older stamens bend away from the central position.

Key Results

The open flowers were visited by a variety of pollinators, most of which were flies. Seed set was pollinator-dependent (bagged flowers set almost no seeds) and pollen-limited (manual pollination increased seed set over open pollination). Analyses of adaptive accuracy showed that coordinated stamen movements and style elongation (movement herkogamy) dramatically increased pollination accuracy. Specifically, dehiscing anthers and receptive stigmas were positioned accurately in the vertical and horizontal planes in relation to the opposite sexual structure and pollinator position. By contrast, the spatial correspondence between anthers and stigma was dramatically lower before the anthers dehisced and after stamens bent outwards, as well as before and after the period of stigmatic receptivity.

Conclusions

It is shown for the first time that a combination of movement herkogamy and dichogamy can maintain high pollination accuracy in flowers with generalized pollination. Staggered pollen and stigma presentation with spatial correspondence can both reduce sexual interference and improve pollination accuracy.     

Stamen movements in flowers ofOpuntia (Cactaceae) favour oligolectic pollinators

Opuntia brunneogemmia andO. viridirubra occur sympatrically in the Serra do Sudeste, Rio Grande do Sul, Brazil. Their flowers have 450–600 thigmonastic stamens and provide large amounts of pollen and nectar for bees. Bees of 41 species were registered at the flowers ofO. brunneogemmia and 30 at the flowers ofO. viridirubra. Females of three oligolectic species are the only effective pollinators:Ptilothrix fructifera (Anthophoridae),Lithurgus rufiventris (Megachilidae), andCephalocolletes rugata (Colletidae). During their visits inOpuntia-flowers, bees touch the filaments and stimulate the movement of the stamens to the centre of the flower. At the end of this movement, the anthers are densely packed around the style. As a consequence the pollen is presented in an easily accessible upper layer of anthers and various, nearly inaccessible lower layers. The lower layers contain about 80% of the pollen reward. Only females of the three oligolectic pollinators exploit the pollen from the lower layers and reach the nectar furrow. Therefore, through their stamen movements,Opuntia flowers hide most of their pollen from flower visitors but favour effectively pollinating, oligolectic bees.     

Fossil flowers and fruits of the Actinidiaceae from the Campanian (Late Cretaceous) of Georgia

A new genus and species of Actinidiaceae (Parasaurauia allonensis gen. et sp. nov.) are established for fossil flowers and fruits from the early Campanian (Late Cretaceous) Buffalo Creek Member of the Gaillard Formation in central Georgia, USA. The fossil flowers, which are exquisitely preserved as charcoal, have five imbricate, quincuncially arranged sepals and petals. The androecium consists of ten stamens with anthers that are deeply sagittate proximally. The gynoecium is tricarpellate, syncarpous, and has three free styles that emerge from an apical depression in the ovary. The fruit is trilocular and contains numerous ovules on intruded axile placentae. The structure of mature fruits is unknown. Comparisons with extant taxa clearly demonstrate that the affinities of Parasaurauia allonensis are with the Ericales, and particularly with the Actinidiaceae, which have been placed among the Ericales in recent cladistic analyses. Because Parasaurauia allonensis is not identical to any one genus of Actinidiaceae, or other member of the Ericales, phylogenetic relationships of the fossil were evaluated through a cladistic analysis using morphological and anatomical characters. Results of this analysis place Parasaurauia allonensis within the Actinidiaceae as sister to the extant genera Saurauia and Actinidia. Parasaurauia allonensis differs from extant Saurauia only in having ten rather than numerous stamens.