Developmental evidence for stamen number reductionin populations of Hibbertia fasciculata (Dilleniaceae)

Discrete Australian populations of Hibbertia fasciculata R. Br. ex DC. differ in stamen number per flower: three to four in isolated, northeastern coastal populations in New South Wales vs. 10–12 in southeastern Australian populations. In all populations, the stamen bases are attached to three broad flat pedestals regardless of number of stamens present. In certain other Hibbertia species, each pedestal results from initiation via a common stamen primordium that usually produces at least 3–4 stamens per common primordium. In H. fasciculata, each of the three pedestals is associated with three to four stamens in flowers of southeastern populations, but with only one stamen per pedestal in the coastal populations of New South Wales. Because the pedestals (remnants of common primordia) have persisted, the evolutionary trend probably has been one of reduction in stamen number. General observations and comparative studies suggest that this population-based reduction series in stamen number (as well as reduced plant size and flower size) reflects a locally successful trend towards smaller organs throughout the plant body together with a shift in pollination ecology.     

The pollination biology ofHibbertia stricta (Dilleniaceae)

The exines of pollen grains ofHibbertia stricta (DC.)R. Br. exF. Muell. (Sect.Pleurandra) wear an oily, yellow pollen coat that stains positively for lipids. The pollen is collected by asocial bees, exclusively. The most common floral foragers are members of the genusLasioglossum (subgenusChilalictus;Halictidae) and they harvest pollen via thoracic vibration. As these bees cling to the inflated anthers their pollen smeared bodies come in contact with either of the two wet, nonpapillate stigmas. The stigmas respond positively to cytochemical tests for the presence of esterase immediately following expansion of the corolla, indicating the effective pollination period. The foraging patterns of the bees are narrowly to broadly polylectic. AsH. stricta flowers are nectarless, it is not surprising that bees bearing mixed pollen loads always carry the pollen of at least one nectariferous, coblooming plant. The pollination biology ofH. stricta is compared with otherHibbertia spp. and with pollen flowers in general.     

Self pollination and resource availability affect ovule abortion inCassia fasciculata (Caesalpiniaceae)

We examined the effects of pollen source and resource availability on ovule abortion in the annual legumeCassia fasciculata. Pollen source was controlled by hand-pollinating flowers with cross- or self-pollen. Resource availability to developing fruits was controlled by adjusting fruit loads (heavy versus light) on each plant and exposing plants to different photoperiod cycles (16 vs 12 h of light; short days favor fruit growth at the expense of vegetative growth). In mature fruits the proportion of ovules expanding (showing some development over virgin ovules) ranged from 89–95% and did not increase with resource availability, suggesting that unexpanded ovules were either unfertilized or obligately aborted shortly after fertilization. The proportion of expanded ovules maturing in mature fruits was near 97% for both self- and crosspollinations in the treatment with highest resource availability (light load, short days) and lower in the remaining treatments, where self-pollination resulted in up to 9% lower seed maturation than cross-pollination. In the latter three treatments a pollen source effect was dependent upon the maternal plant; in some plants selfing increased abortion and in others it did not. Collectively, the results suggest that (1) both pollen source and resource availability affect ovule abortion, (2) at least some abortion is facultative, and (3) when resources are limited, self-pollination increases abortion in some but not all maternal plants.     

Species diversity,ecology and evolution in a primitive Angiosperm genus:Hibbertia (Dilleniaceae)

Among the approximately 130 species ofHibbertia found in Australia, there are tall shrubs, low or trailing shrubs and vines bearing a diversity of leaves as to shape and venation pattern. Flowers are solitary, in leafy cymes or in false spikes, and display various gradual and abrupt transitions from vegetative to reproductive appendages. In the androecium, stamen number is highly variable both between and within species. Some sections have radial symmetry, others bilateral symmetry of the androecium and gynoecium. Follicle number varies from 10 to 1. Basic chromosome numbers of n = 4, 5, 8, 9, 10, 12 and 13 have been found in various sections, and occasional higher numbers, up to n = 64, indicate the presence of polyploidy. Habitats vary from tropical savanna through rain forest margins, wet and dry sclerophyll forests, heaths, sphagnum swamps, and mallee scrub to desert margins. The principal center of diversity is southwestern Australia, less diverse centers are in southeastern and northern Australia. With respect to leaf size, structure and venation; floral symmetry; and chromosome numbers; the diversity found among the species ofHibbertia exceeds that found in all but a few genera of Angiosperms, and is greater than that in any other exclusively woody genus. Nevertheless, individual species are relatively constant with respect to both morphology and ecological preferences.Presented at the symposium Speciation and the Species Concept during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

Relationships between floral organization, architecture, and pollination mode inDillenia (Dilleniaceae)

The flowers ofDillenia are highly elaborate pollen-flowers adapted to buzzpollination byXylocopa bees. Two major forms of floral architecture (revolver flowers and roundabout flowers) are associated with two different pollination modes. In the first (e.g.,D. suffruticosa), the pollination organs are connivent to a cone; the pollinator grasps the entire cone with its legs and buzzes it; it revolves around its axis and repeats the buzzing in different positions. In the second (e.g.,D. alata, D. philippinensis), the stylar branches are spreading and the stamens are arranged in two sets of two different forms and colourations. The inner set has fewer and longer stamens that are cryptic pollination stamens; those of the outer set are shorter but optically conspicuous feeding stamens. The pollinator squeezes itself under the stylar branches and handles only the outer set by grasping part of the set at a time; it moves tangentially around the flower with several buzzing-stops; when buzzing pollen is sprayed onto its side and back from the inner stamen set. Centrifugal polyandrous androecia are a constitutive feature of flowers inDilleniaceae. InDillenia the centrifugal initiation of stamens proceeds for an unusually long time and is still not finished when the gynoecium is completely closed (in contrast toTetracera). The differentiation of heteranthery seems to be functionally correlated with the extended centrifugal inception. The latest formed stamens are small and sterile in many species. Generic features ofDillenia flowers can be understood from the roundabout architecture: big size, increased number of carpels, syncarpy forming a firm pedestal and spreading firm stylar branches with small, concave stigmas at the end, stamens with short, stout filaments and much elongated poricidal anthers, heteranthery, recurved stamens of the inner set.Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday     

Population variation in plant traits associated with ant attraction and herbivory in Chamaecrista fasciculata (Fabaceae)

The benefits of ant–plant–herbivore interactions for the plant depend on the abundance of ants and herbivores and the selective pressures these arthropods exert. In plants bearing extrafloral nectaries (EFN), different mean trait values may be selected for by different populations in response to local herbivore pressure, ultimately resulting in the evolution of differences in plant traits that attract ants as defensive agents against herbivory. To determine if variation in traits that mediate ant–plant interactions reflect herbivore selective pressures, we quantified intra- and inter-population variation in plant traits for eight populations of the EFN-bearing annual Chamaecrista fasciculata (Michx.) (Fabaceae). Censuses in rural and urban areas of Missouri and Illinois (USA) showed population differences in ant attendance and herbivore pressure. Seeds were collected from each population, and plants were grown in a common greenhouse environment to measure sugar production, nectar volume and composition, EFN size and time of emergence, leaf pubescence, and leaf quality throughout plant development. Populations varied mainly in terms of nectary size, sugar production, and nectar volume, but to a lesser degree in leaf pubescence. Populations of C. fasciculata within urban areas (low in insect abundance) had small nectaries and the lowest nectar production. There was a positive correlation across populations between herbivore density and leaf damage by those herbivores on the one hand and sugar production and nectar volume on the other. These results, in conjunction with lack of evidence for maternally based environmental effects, suggest that population differences in herbivore damage have promoted differential evolution of EFN-related traits among populations. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Androecium and floral nectaries ofHarungana madagascariensis (Clusiaceae)

The mature flower ofHarungana madagascariensis (Choisy)Poir. has an androecium of five antipetalous fascicles, consisting of four stamens each. The stamen fascicles alternate with five indented nectary scales. A SEM-study of the floral development, as well as a study of the floral anatomy was carried out to understand whether the nectariferous scales represent staminodia or are receptacular in nature and consequently whether or not the androecium ofHarungana, and theClusiaceae in general, is originally diplostemonous. The five petals originate by the splitting of petal-stamen complexes. Next the upper part of each complex differentiates basipetally in four stamens. The stamens remain fascicled and are lifted on a long stalk at maturity. Five carpel primordia are initiated united in a low ringwall. The five nectary scales appear after carpel inception and develop an external morphology reminiscent of anthers. The floral anatomy reveals an independent origin of sepal median traces and common sepal lateral traces, free petal traces, stamen fascicle traces and alternating vascular tissue which supplies the nectaries. The petal-stamen complexes are the result of a retardation in petal inception, linked with the absorption of petal tissue into the stamen primordia. The development of the stamen fascicles is discussed; it is suggested that they are of a secondary nature and do not appear as a reduction from a multistaminate androecium. The external morphology and vascular anatomy of the scales speaks in favour of a staminodial nature. The comparison with some other species of theClusiaceae gives evidence of a diplostemonous ancestry of the androecium.     

Aspects of floral structure and phenology in the genusConophytum (Mesembryanthemaceae)

The complex floral structure in the southern African genusConophytum (Mesembryanthemaceae; 77 spp.) is described in detail and assigned to three basic floral types, two of which can be divided into two subtypes. Correlations between structural features and phenological patterns are demonstrated and discussed in the family context as well as in relation to the systematic subdivision of the genus.     

Colony dynamics in a primitively eusocial halictine beeLasioglossum (Dialictus) zephyrum (Hymenoptera: Halictidae)

Summary Proximate control of colony dynamics was studied in the primitively eusocial halictine beeLasioglossum (Dialictus) zephyrum using allozyme markers. The results indicate that workers produce on average 15% of the male brood (range=0–50%) in small laboratory colonies made up of unrelated, single-generation, uninseminated females. This proportion is not influenced by colony size, but is influenced by the relative size of the queen. Large queens are more successful in dominating their workers than are small queens, the queen being defined as the female that is the mother of most of the brood produced in the colony. Older and larger females tend to become queens. Thus, while small differences in age (up to 4 days) influence which female becomes a queen, her ability to control her workers is primarily influenced by her relative size. The proportion of reproduction that is co-opted by the queen is negatively correlated with colony reproductivity (the number of males/day/female). Colony reproductivity is also negatively correlated with the standard deviation in size among females.     

Notes onDiphucephala affinis (Coleoptera:Scarabaeidae) associated with flowers ofHibbertia andAcacia in Western Australia

Notes are provided on the association of the beetleDiphucephala affinis (Scarabaeidae) with yellow flowers ofHibbertia hypericoides, H. huegelii (Dilleniaceae),Acacia pulchella, andA. stenoptera (Mimosaceae). Observations were undertaken during September 9–19, 1979 at S. Perth, Western Australia. They indicated thatD. affinis is not a pollinator ofHibbertia as suggested in the literature, but may play a small role in the pollination of someAcacia species.     

洋葱花器数目变异研究

以洋葱JQS-1、MST-140、Red beauty 3个常规栽培品种的鳞茎为试材,观察统计洋葱花器数目的变化,探讨花器数目的变异与植物花器多样性的关系,为植物花器发育模式以及植物分类和系统发育研究提供依据。结果表明:(1)洋葱花序中正常的洋葱小花含有6枚雄蕊,一些异常小花雄蕊的数目减少到5枚或增加到7~11枚;正常花药中的花粉粒数量大、形状规则、分散均匀,而异常花药中的花粉粒形状不规则。(2)雌蕊数目也发生变异,子房由正常的3室,变成了2室、4室或6室;花柱从正常1枚,增加到2枚或3枚。(3)正常小花含有6片花被片,异常小花的花被片数目从5片到10片。(4)花被片与雄蕊数目的变异有同步增减和非同步增加2种类型。     

Observations on pollination inSarcostemma (Asclepiadaceae)

Field observations on pollination in New World species of the genusSarcostemma R. Br. sensuHolm are reported. Morphological and anatomical comparisons of pollinated flowers ofSarcostemma subg.Ceramanthus Kuntze (New World) andSarcostemma subg.Sarcostemma (Old World) are presented.     

The unique pollination ofLeporella fimbriata (Orchidaceae): Pollination by pseudocopulating male ants (Myrmecia urens,Formicidae)

Leporella fimbriata is a self compatible orchid of southern Australia. It is dependant across its range on unique pollination by sexually attracted male winged antsMyrmecia urens, which pseudocopulate with the flower. Typical pollination sequences began with an initial circling then zig-zag flight to the flower. Vectors usually alighted on the inflorescence stem and quickly crawled to the flower where they adopted a copulatory position sideways along the wide labellum, pseudocopulatory probing immediately followed. In this position pollen carried on the thorax was deposited on the stigma. Departure from the labellum usually resulted in pollinium removal. Pollinator movements were restricted and the distribution leptokurtic with a mean of 3.141 ± 4.59 m. Pollination was widespread but variable from site to site and season to season with a maximum of 70% of all flowers being pollinated. Pollinator limitation is indicated. Traits essential for this pollination interaction include the coincidence of orchid and ant geographic distributions and the coincidence of flowering with the flight period of the ant. The production of pheromonelike substances and the distinctive floral morphology are also essential for attraction and manipulation of male ants. The ant mating system which the orchid can exploit is also important.     

The dimorphic heterostyly inAconogonon campanulatum (Polygonaceae)

Heterostyly is clearly confirmed inAconogonon campanulatum. This distylous species is dimorphic for tepals, styles, stigma surface, stamens, pollen grain size, and pollen sexine ornamentation. The floral shape is campanulate and thrum flowers are slightly larger than pin flowers. Small solitary bees were observed as flower visitors and probably effected pollination. The possible evolution of dioecy via heterostyly within the genusAconogonon is discussed.     

Breeding systems and pollination inVigna minima (Leguminosae,Papilionoideae)

Four types of floral breeding systems—(i) chasmogamy, (ii) aerial pseudocleistogamy, (iii) subterranean pseudocleistogamy and (iv) obligate subterranean true cleistogamy—are observed in the populations ofVigna minima inhabiting the Western Ghats (India). Five categories of phenotypes are recognized based on the number and kinds of floral breeding systems found in a given individual. The frequencies of different categories of phenotypes not only show intra- and interpopulation variation, but also fluctuate from generation to generation suggesting differences in the genetic structure of populations. This polymorphism in the breeding system of a single species is unique and may be adaptive. Obligate subterranean true cleistogamy and amphicarpy appear to be adaptations to jungle fires and soil erosion.—The flowers are of the flag-blossom type and insect visitors act as tripping agents. The tripping mechanism together with the polymorphic floral breeding system result in a balanced mixture of selfing and outcrossing. Such a recombination system may enhance the fitness ofV. minima which is essentially a colonizing species.     

Genetic systems of six species ofPlantago (Plantaginaceae)

Investigation of the genetic system of six species ofPlantago has revealed striking differences in their breeding and meiotic systems.Plantago patagonica is an inbreeder on account of preanthesis cleistogamy, whereasP. lanceolata is an obligate outbreeder, as it is self-incompatible.Plantago drummondii, P. lagopus, P. ovata, andP. major show mixed mating but in varying proportions. In terms of their energy budgets, outbreeding species invest more in floral advertisement and male function, while inbreeders invest more in female function. The contribution of the meiotic system to genetic variability, as revealed through recombination index, is more important in the inbreeding species.     

A phylogeny of Cariniana (Lecythidaceae) based on morphological and anatomical data

Cariniana as previously circumscribed is a genus of 16 species restricted to neotropical forest habitats on well-drained sites. A phylogenetic analysis of the genus based on 33 morphological and anatomical characters was undertaken. The results show that Cariniana consists of two clades: the Allantoma/Cariniana decandra clade includes Allantoma lineata and seven species of actinomorphic-flowered Cariniana and is characterized by 5-merous flowers, carnose petals, incurved petal apex, scarcely lobed calyces, eucamptodromous secondary veins, dichotomizing venation, and poorly developed areolation; the C. legalis clade is made up of nine species and is characterized by an obliquely zygomorphic androecium, reticulate tertiary venation, and anomocytic stomata. The actinomorphic-flowered Cariniana are more closely related to the monotypic Allantoma lineata than they are to the species of the C. legalis clade. In order to reflect these relationships, Cariniana is divided into two genera: species in the C. legalis clade, which includes the generic type C. legalis, remain as Cariniana while species of Cariniana in the Allantoma/Cariniana decandra clade are transferred to Allantoma. The following new combinations are proposed: Allantoma decandra, A. integrifolia, A. kuhlmannii, A. pluriflora (a nomen novum for Cariniana multiflora because Allantoma multiflora is a synonym of Couratari multiflora), A. pachyantha, A. pauciramosa, and A. uaupensis.     

Corolla and androecium development in someEudesmia eucalypts (Myrtaceae)

In the early stages of ontogeny, the corolline parts of theEudesmia eucalypts develop as compound structures directly comparable to the early stages of the petals ofAngophora and the bloodwood eucalypts, but with the onset of androecial formation a marked difference takes place. Rather than forming on the floral apex, the stamen primordia arise on the basal adaxial components of the young corolline parts; this basal component develops into the staminophore of the mature flower. The operculum consists only of the dorsal components of the corolline parts, the homologues of the dorsal keels of theAngophora petals. If the corolline parts remain more or less free in their early developmental stages, corresponding groups of stamens are produced. Early corolline continuity leads to a continuous ring of stamens. The staminophore is not an organ sui generis, but a derivative of the corolla. The bundles of stamens in some species are best referred to as epipetalous groups, not antepetalous fascicles.     

Notes on the pollination mechanisms ofMoraea inclinata andM. brevistyla (Iridaceae)

Individual flowers ofMoraea inclinata are nectariferous and last about six hours. They appear to be pollinated largely by bees in the familyHalictidae (Lasioglossum spp.,Nomia spp.,Zonalictus) and to a lesser extent by bees in the familyAnthophoridae (Amegilla). The mechanism of bee-pollination inM. inclinata is the Iris type; i.e., each flower consists of three pollination units (an outer tepal, a partly exserted anther, and the opposed style branch which terminates in a pair of petal-like crests). Bees rarely visit more than one pollination unit per flower. Transferral of pollen to the bee is passive and nototribic although all bees collected on the flowers were female and 55% of the bees carried pollen loads with 2–5 pollen taxa in their scopae.Moraea brevistyla flowers are nectariferous but lack scent and last two days. They are visited infrequently by bees and only one femaleLasioglossum spec. carried the pollen ofM. brevistyla. Unlike flowers ofM. inclinata those ofM. brevistyla deposit pollen only on the head and thorax. Bee-mediated autogamy in both species is avoided due to the erratic foraging patterns of the bees and the flexibility of each stigma lobe as the bee backs out of the flower. Approximately 2–4 flowers in the inflorescences of both species (6–8 flowers/infloresence) develop into capsules.     

Two new species ofPhyllagathis related toP. tuberculata (Melastomataceae) from Peninsular Malaysia

Phyllagathis tuberculata King and two closely allied new species,P. magnifica A. Weber andP. stonei A. Weber, are described and illustrated. Within the genus, these species form a distinct and isolated group which is restricted to Peninsular Malaysia.P. tuberculata occurs in Perak (probably confined to G. Bujang Melaka),P. magnifica andP. stonei are found in the mountains on the Pahang/Selangor border (Genting Highlands, Gombak valley). The distinctive characters of the three species are listed and some general information relating to inflorescence morphology, tubercle anatomy, fruit structure and seed dispersal is provided.