Floral morphology of southern African Orchideae. I. Orchidinae

The floral morphology of the southern African genera of Orchidaceae-Orchideae-Orchidinae ( Brachycorythis, Schwartzkopffia, Neobolusia, Schizochilus, Holothrix and Bartholina ) is surveyed paying special attention to the gynostemium. Ontogenetic data are provided for a number of species that appear to be essential in formulating a proper interpretation of the gynostemium. The floral architecture is shown to be basically similar to that of the (much better known) European representatives of the subtribe. This, however, does not fully apply to the homology of the lateral gynostemium appendages ("auricles"): In Brachycorythis, Neobolusia and Schizochilus these develop like in Orchis and Dactylorhiza. Their prominent sculptured portions originate from dorsal stamen outgrowths and correspond to filament excrescences. Structures obviously homologous to lateral inner stamens can be recognized in the early ontogeny, but are in the mature flower incorporated in the 'arch' connecting the lip with the gynostemium. In contrast, in Holothrix and Bartholina the gynostemium appendages correspond entirely to staminodes, while the filament excrescences are missing. It is also shown that the 'concave' stigma said to be characteristic of the Orchidinae is in fact ± convex or even pad-like, but is generally positioned in a cavity under the rostellum. The 'erect' anther (the main diagnostic feature of the Orchideae) is reflexed up to 45° in some taxa. Affinities of the genera are briefly discussed. The generic separation of Schwartzkopffia and Neobolusia from Brachycorythis does not appear justified. Neobolusia virginea is obviously misplaced in the respective genus, and eventually merits generic status. The affinities of Schizochilus remain ± obscure at the moment. Bartholina appears to be merely a small group of specialized Holothrix species.     

The gynostemium of Hemipiliopsis purpureopunctata and Senghasiella glaucifolia, two taxonomically disputed species of Habenariinae (Orchidaceae)

The gynostemium structure and ontogeny of two taxonomically disputed orchids, Hemipiliopsis (= Habenaria ) purpureopunctata and Senghasiella (= Habenaria ) glaucifolia , are described and illustrated by scanning electron micrographs. The early gynostemium ontogeny of Hemipiliopsis purpureopunctata is shown to be fundamentally similar to that of the species of the tribe Orchideae that have been previously studied. This includes the initiation sequence of sepals, petals and lip, form and orientation of anthers, three-lobed condition of median carpel apex, and presence of auricles and basal bulges. During the later developmental stages some differences occur. The stigma processes of Senghasiella glaucifolia are united into a tongue-shaped organ, and the lateral rostellum lobes of Hemipiliopsis purpureopunctata protrude forwards with their viscidia positioned above the spur-mouth. Based on gynostemium characters, the generic rank of Hemipiliopsis was confirmed, but that of Senghasiella was not supported.  © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society , 2005, 147 , 191–196.     

Molecular phylogenetics of Diseae (Orchidaceae): a contribution from nuclear ribosomal ITS sequences

We present here the first molecular phylogeny of tribe Diseae (Orchidoideae: Orchidaceae). Nuclear ribosomal ITS1, 5.8S rDNA, and ITS2 sequences were compared for 30 Diseae, 20 Orchideae, and four Cranichideae and Diurideae outgroups. ITS - rDNA sequences exhibited a transition:transversion ratio of 1.3 and extensive ITS length polymorphism. Phylogenetic analyses using maximum parsimony identified seven major core orchidoid groups. The branching order of the five Diseae and two Orchideae clades was weakly supported but indicated paraphyly of Diseae, with Disperis sister to the rest, followed by successive divergence of Brownleea, Disinae, Coryciinae sensu stricto (s.s.), Satyriinae, and terminated by Orchidinae plus Habenariinae. Within the monophyletic Disinae, Herschelia and Monadenia were nested within a paraphyletic Disa and clustered with D. sect. Micranthae. Within monophyletic Satyriinae, Satyridium rostratum plus Satyrium bicallosum was sister to the rest of Satyrium, and then Satyrium nepalense plus S. odorum was distinct from a cluster of six species. Coryciinae are paraphyletic because Disperis is sister to all other core orchidoids. Coryciinae s.s. are sister to Satyriinae plus Orchideae, with Pterygodium nested within Corycium. Maximum likelihood analysis supported possible affinities among Disinae, Brownleeinae, and Coryciinae but did not support monophyly of Diseae or an affinity between Disinae and Satyriinae. Morphological characters are fully congruent with the well-supported groups identified in the ITS phylogeny.     

Developmental studies in orchid flowers II: Orchidoid species

The floral development of 11 species of Orchidoideae (sensu Rasmussen 1985) was studied by means of SEM, paying special attention to the early development of the gynostemium and its appendages. In contrast to the staminodes found in epidendroid and vandoid orchids, the 'auricles' of the tribe Orchideae are developed on the dorsal side of the fertile anther and therefore are not interpreted as staminodes. Presumed vestiges of the staminodes corresponding to those of the Epidendroideae and Vandoideae are differentiated in early developmental stages, but remain inconspicuous structures later on. The three-lobed rostellum originates entirely from the median carpel. The outstanding systematic position of the tribe Orchideae is briefly discussed.     

Floral morphology and ontogeny in Orchidaceae subtribe Disinae

Floral morphology and ontogeny in Orchidaceae subtribe Disinae. The flower structure and development of 24 species of the orchid subtribe Disinae are described and illustrated by drawings and scanning electron micrographs with special attention being paid to the gynostemium. The morphogenesis of this subtribe is fundamentally similar to that of the closely related tribe Orchideae. This includes the initiation of the auricles on the anther base in a dorsolateral position, and hence their interpretation as being mere appendages of the filament. The keel connecting the petals and the gynostemium plus its protrusion is considered homologous to the inner lateral staminodeS. Presumed vestiges of the adaxial staminodes were detected in one specieS. A peculiarity of the Disinae is that the entire apex of the median carpel develops into the rostellum, whereas its stigmatic portion emerges from the median carpel below the rostellum in later stages. The main diagnostic feature of the group is the reflexed position of the mature anther. However, it is shown here that this anther movement occurs in the later stages and that the initial anther is erect.     

Cytological studies on some representative species of the tribe Orchideae (Orchidaceae) from China

Cytological studies were carried out on 14 taxa belonging to Amitostigma , Chusua , Galearis , Habenaria , Hemipilia , Hemipiliopsis , Herminium , Peristylus and Ponerochis , collected mostly from the south-eastern part of the Hengduan Mountain Region, south-west China. Cytological data on 11 of the taxa are reported for the first time. The interphase nuclei were either of the simple chromocentre type or intermediate between simple and complex chromocentre types. The nuclear morphology of Hemipiliopsis at interphase supports the conclusion that it is related more closely to Chusua and Ponerochis than to Habenaria . At the whole tribe level, however, the results did not indicate a clear correlation between morphological features of the interphase nuclei and phylogeny. The somatic chromosome numbers were 2 n  = 42 in ten species and 2 n  = 32, 38, 40, 64 and 72 in four species. The chromosome counts of 2 n  = 32 and 64 in Habenaria aitchsonii are rare in the genus. It is proposed that the repeated change of chromosome number from x  = 7 to x  = 8 has played an important role in the evolution of the tribe Orchideae. This change has occurred mainly in the European subtribe Orchidinae, but also in the Asian subtribe Habenariinae.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 145 , 231–238.     

Developmental studies in orchid flowers III: Neottioid species

The floral development of 19 species of Neottioideae (sensu Rasmussen 1985) was studied by means of scanning electron microscopy, paying special attention to the early differentiation of the organs that constitute the gynostemium. The gynostemium development of the Epipactieae proved to be similar to that of the Epidendroi deae and Vandoideae, in particular in that massive primordia corresponding to inner lateral staminodes are differentiated in early stages and later constitute the lateral appendages of the gynostemium. In the Neottieae a progressive reduction and delayed initiation of these staminodes was observed: the lateral teeth of the gynostemium originate from large staminode primordia in one species ( Corymborkis veratrifolia ), in the remaining species they are initiated in later stages or are missing.     

The floral morphology and ontogeny of some Chinese representatives of orchid subtribe Orchidinae

The flower structure and development of ten species in six genera of the orchid subtribe Orchidinae are described and illustrated by scanning electron micrographs. Particular attention is given to the structure of the gynostemium, which for most species is interpreted from ontogenetic data. All the species studied here share a series of features, e.g. the sequence of tepal and anther initiation, the shape and position of the anther, the presence of auricles and basal bulges, the three-lobed condition of the median carpel apex and the lateral lobes of the median carpel embracing the basal ends of the thecae. However, the form and structure of the three carpel apices are most varied in the later development stages or in the adult flower. The genus Hemipilia shows a series of peculiar characters that are quite different from those of the other genera in Orchidinae. The peculiar structure and development of the viscidia in both Amitostigma and Neottianthe indicate that both of them are different from other genera in Orchidinae. The adult floral morphology shows that the genera Galearis and Chusua are not congeneric with Orchis. The separation of the lateral lobes of the rostellum in most genera studied here as well as in the Brachycorythis group from South Africa suggests that this is the ancestral state in the subtribe Orchidinae. In contrast, the conjoining of lateral lobes in Dactylorhiza and Orchis is suggested as a derived character.     

Phylogenetic relationships in Disa based on non-coding trnL-trnF chloroplast sequences: evidence of numerous repeat regions

Sequence data from the intron and spacer of the trnL-F chloroplast region elucidate the phylogenetic relationships of the tribe Diseae (Orchidoideae: Orchidaceae). Within Diseae, 41 species of Disa, two of Brownleea, three of Satyrium, and two of Corycium were included, with five species of Habenaria sensu lato (Orchideae) and one epidendroid as outgroups. The sequences revealed substitutions and considerable length variation, due mainly to the presence of repeat motifs. Phylogenetic analysis using parsimony revealed five distinct clades. The branching order of the five weakly supported the paraphyly of Diseae, with the successive divergence of Brownleea, Corycium, Habenaria, Satyrium, and Disa. Within the monophyletic Disa, three main groupings appeared, two strongly supported clades representing sect. Racemosae and sect. Coryphaea and the third grouping containing several clades currently grouped into sections based on morphological phylogenies. Some discrepancies between the molecular phylogeny and the phylogeny based on morphological characters may require reevaluation of some of the morphological characters. The presence of different numbers of repeat motifs, both among different taxa and within taxa, indicates that these characters may be phylogenetically informative at the population level.     

Developmental studies in orchid flowers I: Epidendroid and vandoid species

The floral development of 47 epidendroid and vandoid orchids was studied by means of scanning electron microscopy, paying special attention to the early development of the gynostemium (column) and its appendages. The following main conclusions are drawn: the lateral appendages of the adult gynostemium are homologous with the two lateral stamens of the inner whorl; their primordia are present even in species which lack prominent appendages in the adult gynostemium (incorporation of the sta-minodial primordia into the gynostemium during development). Ventral appendages observed in some species are supposed to be vestiges of the adaxial stamens on account of their early initiation. It is confirmed that the rostellum is the upper part of the median stigma lobe and that the lip corresponds to the inner median tepal. The affinities of the epidendroid and vandoid orchids are briefly discussed.     

Hawkmoth pollination of Bonatea speciosa (Orchidaceae) in a South African coastal forest

Hawkmoths ( Theretra capensis and Hyles lineata livornica ) pollinated the orchid Bonatea speciosa at a forested site along the southern Cape coast of South Africa. The flowers of B. speciosa are strongly evening-scented and hawkmoth activity was confined to a short period of 40 minutes after dusk on each evening of observation. The pollinaria are exceptionally elongated (c. 20 mm in length) and are affixed to the eyes of the hawkmoths. Pollinaria attached to feeding hawkmoths are brushed over the long stigmatic arms which project in front of flowers. The flowers of B. speciosa have a toothlike process at the mouth of the spur which forces moths to enter the flower from either side. As a result, only one of the pollinaria is removed from the flower during a visit. The division of the flower into two functional units by the toothlike process in the spur distinguishes the floral mechanism of B. speciosa from other Habenariinae.     

Floral ontogenetic evidence of repeated speciation via paedomorphosis in subtribe Orchidinae (Orchidaceae)

Thoroughly sampled molecular phylogenies of the dominantly European orchid subtribe Orchidinae were used to identify a pair and a triplet of recently diverged species in which: (1) divergence involved substantial changes in floral morphology, particularly in the labellar lobes and spur; and (2) the polarity of those changes could be inferred phylogenetically. Floral ontogeny in the selected species was documented in detail through macromorphological, light microscopic, and scanning electron microscopic study of a wide range of ontogenetic stages. All study species showed differentiation of perianth segments earlier than the gynostemium. Unsurprisingly, component parts of the basic floral organs (gymnostemial auricles and rostellum, labellar lateral lobes, and spur) were initiated relatively late, the spur and ovary continuing to expand beyond anthesis. The predominant evolutionary pattern identified in the two case studies was paedomorphosis via progenesis (earlier offset of growth); this credibly explained the reduction in spur size and lateral lobing of the labellum in Gymnadenia odoratissima and, especially, G. austriaca relative to G. conopsea. Loss of resupination in G. austriaca was best viewed as the deletion of a formerly terminal ontogenetic stage. Radical reduction of the spur of Dactylorhiza viridis relative to D. fuchsii was also attributed to progenesis, although the long, narrow outline and relatively short central lobe of its labellum were attributed to increased growth of the lateral lobes (i.e. hypermorphosis resulting in peramorphosis). Microscopic study of epidermal cell types on the labellum and spur suggested a degree of decoupling of micromorphological from macromorphological transitions, although both were subject to heterochronic shifts. Each of the two case studies was consistent with, but not proof of, saltational macroevolution operating via functional changes in one or more key developmental genes. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 157 , 429–454.     

A morphometric analysis of the Bonatea speciosa complex (Orchidaceae) and its implications for species boundaries

Species boundaries in rapidly evolving lineages are often blurred, necessitating analysis of the full range of variation within a complex in order to identify traits that can be used to diagnose taxa. The delimitation of Bonatea speciosa (L. f.) Willd. has been controversial, as most, but not all, recent authors have included within the concept of this species several additional taxa that were formerly recognised at the species level, including Bonatea boltonii (Harv.) Bolus and Bonatea antennifera Rolfe. Morphological variation across the Bonatea speciosa complex (Orchidaceae) was explored using principal component and cluster analysis. Scatter plots were used to identify characters that could potentially be used to diagnose taxa. These data support the recognition of three distinct species, B. speciosa , B. antennifera and B. boltonii , instead of a single entity. A taxonomic account of southern African taxa within the B . speciosa complex is presented.     

寒兰花器官发生及花发育过程的研究

为了揭示寒兰的成花机理,利用石蜡切片和花芽实体解剖记录了濒危植物寒兰花芽分化和发育的过程,并着重观察唇瓣和合蕊柱早期及中期的发育(在合蕊柱伸长之前)。结果表明:寒兰花芽分化沿着花序轴从下往上可分为4个阶段:花序原基分化,花原基分化,花被片分化和合蕊柱形成。唇瓣分化分为3个阶段:褶片分化,侧裂片分化和色块形成。唇瓣侧裂片和褶片产生较晚,与退化雄蕊可能没有关系。在合蕊柱形成过程中,首先分化出花药,随后分化产生中心皮顶部,侧心皮顶部,并形成花柱道,最终分化出蕊喙和黏盘。     

Molecular phylogenetics and evolution of Orchidinae and selected Habenariinae (Orchidaceae)

Internal transcribed spacer (ITS nuclear rDNA) data have been obtained from 190 terrestrial orchid species, encompassing all genera and the great majority of the widely recognized species of Orchidinae, a heterogeneous selection of species of Habenariinae, and single species of Satyriinae and Disinae (the latter serving as outgroup). The resulting parsimony‐based phylogeny reveals 12 well‐resolved clades within the Orchidinae, based on Anacamptis s.l., Serapias, Ophrys, Steveniella–Himantoglossum s.l. (including ‘Comperia’ and ‘Barlia’, most species being 2n = 36), Neotinea s.l., Traunsteinera–Chamorchis, Orchis s.s., Pseudorchis–Amerorchis–Galearis–Neolindleya–Platanthera s.l. (most 2n = 42), Dactylorhiza s.l., Gymnadenia s.l. (most 2n = 40, 80), Ponerorchis s.l.–Hemipilia s.l.–Amitostigma–Neottianthe, and Brachycorythis (most 2n = 42). Relationships are less clearly resolved among these 12 clades, as are those within Habenariinae; the subtribe appears either weakly supported as monophyletic or as paraphyletic under maximum parsimony, and the species‐rich genus Habenaria is clearly highly polyphyletic. The triphyly of Orchis as previously delimited is confirmed, and the improved sampling allows further generic transfers to Anacamptis s.l. and Neotinea s.l. In addition, justifications are given for: (1) establishing Steveniella as the basally divergent member of an appreciably expanded Himantoglossum that incorporates the former genera ‘Barlia’ and ‘Comperia’, (2) reuniting ‘Piperia’ with a broadly defined Platanthera as section Piperia, necessitating ten new combinations, (3) broadening Ponerorchis to include Chusua, and Hemipilia to include single ‘orphan’ species of Ponerorchis and Habenaria, and (4) recognizing ‘Gymnadenia’camtschatica as the monotypic Neolindleya camtschatica within the Pseudorchis～Platanthera clade. Few further generic transfers are likely in Orchidinae s.s., but they are anticipated among habenariid genera, on acquisition of additional morphological and molecular evidence; one probable outcome is expansion of Herminium. Species‐level relationships are also satisfactorily resolved within most of the major clades of Orchidinae, with the notable exceptions of Serapias, the derived sections of Ophrys, Himantoglossum s.s., some sections within Dactylorhiza, the former genus ‘Nigritella’ (now tentatively placed within Gymnadenia s.l.), Hemipilia s.l., and possibly Ponerorchis s.s. Relationships among the 12 major clades broadly accord with bona fide records of intergeneric hybridization. Current evidence supports the recently recognized 2n = 36 clade; it also indicates a 2n = 40 clade that is further diagnosed by digitate root‐tubers, and is derived relative to the recently recognized clade of exclusively Asian genera (Ponerorchis s.l.–Hemipilia s.l.–Amitostigma–Neottianthe). This in turn appears derived relative to the Afro‐Asiatic Brachycorythis group; together, these two clades identify the plesiomorphic chromosome number as 2n = 42. If the African genus Stenogolottis is correctly placed as basally divergent within a monophyletic Habenariinae, the tribe Orchideae and subtribes Orchidinae and Habenariinae could all have originated in Africa, though in contrast the Asiatic focus of the basally divergent members of most major clades of Orchidinae suggests an Asiatic radiation of the subtribe. Morphological characters informally ‘mapped’ across the molecular phylogeny and showing appreciable levels of homoplasy include floral and vegetative pigmentation, flower shape, leaf posture, gynostemium features, and various pollinator attractants. Qualitative comparison of, and reciprocal illumination between, degrees of sequence and morphological divergence suggests a nested set of radiations of progressively decreasing phenotypic magnitude. Brief scenarios, both adaptive and non‐adaptive, are outlined for specific evolutionary transitions. Recommendations are made for further species sampling, concentrating on Asian Orchidinae (together with the Afro‐Asiatic Brachycorythis group) and both Asian and Southern Hemisphere Habenariinae, and adding plastid sequence data. Taxonomic changes listed are: Anacamptis robusta (T.Stephenson) R.M.Bateman, comb. nov. , A. fragrans (Pollini) R.M.Bateman, comb. nov. , A. picta (Loiseleur) R.M.Bateman, comb. nov. , Neotinea commutata (Todari) R.M.Bateman, comb. nov. , N. conica (Willdenow) R.M.Bateman, comb. nov. , Platanthera elegans Lindley ssp. maritima (Rydberg) R.M.Bateman, comb. nov. , P. elegans Lindley ssp. decurtata (R.Morgan & Glicenstein) R.M.Bateman, comb. nov. , P. elongata (Rydberg) R.M.Bateman, comb. nov. , P. michaelii (Greene) R.M.Bateman, comb. nov. , P. leptopetala (Rydberg) R.M.Bateman, comb. nov. , P. transversa (Suksdorf) R.M.Bateman, comb. nov. , P. cooperi (S.Watson) R.M.Bateman, comb. nov. , P. colemanii (R.Morgan & Glicenstein) R.M.Bateman, comb. nov. , P. candida (R.Morgan & Ackerman) R.M.Bateman, comb. nov. and P. yadonii (R.Morgan & Ackerman) R.M.Bateman, comb. nov. © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society, 2003, 142 , 1–40.     

Elaborate petals in Australian Spermacoce (Rubiaceae) species: morphology, ontogeny and function

BACKGROUND AND AIMS: Australian Spermacoce species display various types of elaborate petals. Their precise morphology, ontogenetic origin, and function are hitherto unknown. The aim of the present paper is to unravel the development and nature of the diverse types of elaborate petals in Spermacoce through a floral ontogenetic study. METHODS: The floral ontogeny of six species characterized by different types of corolla appendages was studied by scanning electron microscopy and light microscopy. In order to elucidate the possible functions of the elaborate petals, field observations were conducted as well. KEY RESULTS: Scanning electronmicrographs show that full-grown petals of Spermacoce lignosa, S. phaeosperma and S. redacta bear appendages on their ventral side. Despite their different appearance at anthesis, the appendages develop very similarly in all three species. They are initiated at the same developmental stage and are first visible as two arcs of primordia converging from the upper margins of the petal towards its midvein and downwards. In S. brevidens, S. caudata and S. erectiloba, the full-grown petals have two long, concave protuberances, which develop from the tissue at both sides of the petal's mid-vein. In these three species, initiation of appendages on the ventral side of the petals is also observed, but they are hardly visible on the mature petals. The two types of elaborate petals tightly enclose the anthers, both in bud and during most of the flowering period. CONCLUSIONS: Among Australian Spermacoce species, two types of elaborate petals can be distinguished. The former hypothesis that the two types of elaborate petals are essentially homologous is here rejected. Field investigations point out that the elaborate petals might play a role in the pollination biology of the species.     

Phylogenetics of tribe Orchideae (Orchidaceae: Orchidoideae) based on combined DNA matrices: inferences regarding timing of diversification and evolution of pollination syndromes

Background and aims

Tribe Orchideae (Orchidaceae: Orchidoideae) comprises around 62 mostly terrestrial genera, which are well represented in the Northern Temperate Zone and less frequently in tropical areas of both the Old and New Worlds. Phylogenetic relationships within this tribe have been studied previously using only nuclear ribosomal DNA (nuclear ribosomal internal transcribed spacer, nrITS). However, different parts of the phylogenetic tree in these analyses were weakly supported, and integrating information from different plant genomes is clearly necessary in orchids, where reticulate evolution events are putatively common. The aims of this study were to: (1) obtain a well-supported and dated phylogenetic hypothesis for tribe Orchideae, (ii) assess appropriateness of recent nomenclatural changes in this tribe in the last decade, (3) detect possible examples of reticulate evolution and (4) analyse in a temporal context evolutionary trends for subtribe Orchidinae with special emphasis on pollination systems.

Methods

The analyses included 118 samples, belonging to 103 species and 25 genera, for three DNA regions (nrITS, mitochondrial cox1 intron and plastid rpl16 intron). Bayesian and maximum-parsimony methods were used to construct a well-supported and dated tree. Evolutionary trends in the subtribe were analysed using Bayesian and maximum-likelihood methods of character evolution.

Key Results

The dated phylogenetic tree strongly supported the recently recircumscribed generic concepts of Bateman and collaborators. Moreover, it was found that Orchidinae have diversified in the Mediterranean basin during the last 15 million years, and one potential example of reticulate evolution in the subtribe was identified. In Orchidinae, pollination systems have shifted on numerous occasions during the last 23 million years.

Conclusions

The results indicate that ancestral Orchidinae were hymenopteran-pollinated, food-deceptive plants and that these traits have been dominant throughout the evolutionary history of the subtribe in the Mediterranean. Evidence was also obtained that the onset of sexual deception might be linked to an increase in labellum size, and the possibility is discussed that diversification in Orchidinae developed in parallel with diversification of bees and wasps from the Miocene onwards.     

Ontogenetic origins of floral bilateral symmetry in Moringaceae (Brassicales)

Floral morphology of the 13 species of Moringa ranges from actinomorphic flowers with little hypanthium to highly zygomorphic flowers with well-developed hypanthia. Scanning electron and light microscopy were used to identify ontogenetic differences among two actinomorphic and eight zygomorphic species. All species show traces of zygomorphy between petal organogenesis and anther differentiation. At late organogenesis, zygomorphy is manifest by one petal being larger than the others, slight unidirectional maturation of the anthers, and in many species, some staminodes may be missing. At organ differentiation and beyond, the actinomorphic species show a trend toward increasing actinomorphy, whereas the zygomorphic features of early ontogeny are progressively accentuated throughout the ontogeny of the zygomorphic species. Because of the early traces of zygomorphy throughout the family, ontogeny in Moringa does not resemble that known from the sister taxon Caricaceae, which has flowers that are actinomorphic throughout ontogeny. Great intraspecific variation was found in floral plan in the actinomorphic-flowered species in contrast to the zygomorphic species. Each of the main clades in the family is distinguished by at least one feature of floral ontogeny. In general, ontogenetic differences that are congruent with deeper phylogenetic splits tend to occur earlier in ontogeny than those congruent with more recent divergences.     

Presence of the anther gland is a key feature in pollination of the early‐branching papilionoids Dipteryx alata and Pterodon pubescens (Leguminosae)

• The presence of glandular appendages in the anthers is a rare condition in angiosperms. In Leguminosae it occurs in species of the Mimosoid clade and in early‐branching clades of papilionoids such as Dipterygeae. In Dipterygeae such appendages surprisingly exhibit a secretory cavity instead of secretory emergences as is the case for the Mimosoid clade. Thus, the objective of this study was to elucidate the function of anther glands in Dipteryx alata and Pterodon pubescens, species in the Dipterygeae clade that exhibit a pollen release mechanism that is intermediate between the explosive and valvular types.
• Flower buds and flowers were processed for surface, anatomical, histochemical and ultrastructural analyses.
• Anther glands consist of a cavity secreting sticky substances (oleoresins and polysaccharides) that play a key role during the flower's lifespan by aggregating pollen grains and attaching them to the floral visitor's body. Other floral features that are important for understanding the pollen release mechanism that is intermediate between the valvular and the explosive types are: (i) keel petals intertwined with tector trichomes; (ii) glandular appendages in the abaxial and lateral sepals and in petals composed of secretory ducts; and (iii) a continuous secretion process of the anther glands followed by an asynchronous dehiscence of anthers.
• The well‐adapted papilionoid flag blossom with anther glands and keel petals intertwined with trichomes provided the foundation for a successful canalisation toward a pollen release mechanism intermediate between the explosive and valvular types inside early‐branching papilionoids.

     

Reproductive Biology of <Emphasis Type="Italic">Asarum sieboldii Miq</Emphasis>.

The seasonal developmental rhythm, floral and fruit morphology, anthesis, and fructification of Asarum sieboldii were studied in a natural plant community in the southern part of the Russian Far East. The flower structure was investigated in ditails. It was found that the flower does not have a gynostemium. The flowers are protogynous. At the first anthesis stage, the anthers are closed and cross-pollination may be realized by ants (Hymenoptera) or flies (Dolichopodidae, Diptera). At the second stage of anthesis, there is direct contact of anthers with the pistil stigma and self-pollination occurs. The perianth is involved in the formation of fruit. The fruit is a six-locular, fleshy, half-inferior capsule. Asarum sieboldii has a high productivity of fruits and seeds. The fruit set is 89% after self-pollination. Viable seeds per fruit is 29 ± 2, the seed set is 69 ± 5%. The agents of seed dissemination are ants: Leptothorax acervorum and Myrmica ruginodis (Formicidae, Hymenoptera).