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.     

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.     

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。     

Trends in evolution of floral ontogeny in Cassia sensu stricto,Senna, and Chamaecrista (Leguminosae: Caesalpinioideae: Cassieae: Cassiinae); a study in convergence

Distinctions in floral ontogeny among three segregate genera (Cassia sensu stricto, Chamaecrista, and Senna) of Cassia L. support their separation. In all species studied, the order of floral organ initiation is: sepals, petals, antesepalous stamens plus carpel, and lastly antepetalous stamens. Sepal initiation is helical in all three genera, which however differ in whether the first sepal is initiated in median abaxial position (Senna), or abaxial and off-median (Cassia javanica), a rare character state among legumes. Order of petal initiation varies: helical in Senna vs. unidirectional in Cassia and Chamaecrista. Both stamen whorls are uniformly unidirectional. Intergeneric ontogenetic differences occur in phyllotaxy, inflorescence architecture, bracteole formation, overlap of initiation among organ whorls (calyx/corolla in Cassia; two stamen whorls in Chamaecrista), eccentric initiation on one side of a flower, anther attachment, anther pore structure, and precocious carpel initiation in Senna. The asymmetric corolla and androecium in Chamaecrista arise by precocious organ initiation on one side (left or right). The poricidal anther character can result from differing developmental pathways: lateral slits vs. sealing of lateral sutures; clasping hairs vs. sutural ridges; terminal pores (one or two) vs. none; and clamp layer formation internally that prevents lateral dehiscence. Genera differ in corolla aestivation patterns and in stigma type. Convergence is shown among the three genera, based on intergeneric dissimilarities in early floral ontogeny (floral position in the inflorescence, bracteole presence, position of the first sepal initiated, order of petal initiation, asymmetric initiation, overlap between whorls, anther morphology, and time of carpel initiation) resulting in similarities at anthesis (showy, mostly yellow salverform flowers, heteromorphic stamens, poricidal anther dehiscence, bee pollination, and chambered stigma).     

Floral morphology of southern African Orchideae. II. Habenariinae

The floral morphology of the southern African genera of Orchideae-Habenariinae (Bonatea, Cynorkis, Habenaria, Platycoryne, Stenoglottis, Centrostigma and Roe-perocharis) is surveyed paying special attention to the gynostemium. Ontogenetic data are provided for the species from which adequate material was available. It is shown that the floral architecture is essentially an elaboration and complication of that found in the better known Orchidinae. The structural similarities are particularly evident in the early ontogeny. Although the tribe Orchideae is commonly said to have gynostemia with erect anthers, a few Habenariinae are reported here to have reflexed anthers. In most cases both 'auricles' (filament excrescences) and 'basal bulges' (staminodes) are united to form the lateral gynostemium appendages. The primordia of both structures are clearly recognizable in the early ontogeny in all species studied. In Habenaria dregeana the basal bulges are only basally fused to the auricles, but in their main portion become adnate to the lip and petal bases: the auricles then solely form the lateral gynostemium appendages. It is suspected that this occurs also in other species not studied here. Systematic and phylogenetic aspects of the southern African representatives of the Habenariinae are discussed: the generic separation of Bonatea, Platycoryne and Centrostigma from Habenaria does not appear justified. Cynorkis, Roeperocharis and Stenoglottis are morphologically dissimilar to Habenaria. Based on the findings in the southern African taxa the status of the Habenariinae, Orchidinae, Orchideae and Diseae is discussed: there is no clear distinction between Habenariinae and Orchidinae; while the Diseae seem to represent a monophyletic group, the Orchideae are possibly polyphyletic.     

<Emphasis Type="Italic">Anacamptis</Emphasis> versus <Emphasis Type="Italic">Orchis</Emphasis> (Orchidaceae): seed micromorphology and its taxonomic significance

Seed micromorphology of 24 taxa of the genera Anacamptis and Orchis was examined under light and scanning electron microscopy. Seed qualitative characters appear very useful at the supraspecific level in the subtribe Orchidinae. Based on our observations, the sculpturing of the periclinal walls of the medial testa cells, the seed shape and several features of the anticlinal walls of the apical cells showed variability between the studied taxa, with special relevance of the first character. According to this factor, we found one type of seed for Anacamptis and two for Orchis. The taxonomic value of seed coat characters is compared with the last taxonomic proposals for the genera Anacamptis and Orchis.     

Comparative floral ontogenies among Persoonioideae including Bellendena (Proteaceae)

Floral ontogeny is described and compared in five species and four genera of the hypothetically basal proteaceous subfamily Persoonioideae sensu Johnson and Briggs. The hypotheses surrounding the origin of the peculiar proteaceous flower and homologous structures within the flowers are examined using ontogenetic morphological techniques. Ontogenetic evidence reveals that the proteaceous flower is simple, composed of four tepals, each tepal initiated successively with the lateral tepals being initiated first and second followed by the successive initiation of the sagittal tepals. Each of four stamens is initiated opposite a tepal in a similar sequence to tepal initiation. A single carpel develops terminally from the remaining floral meristem. In taxa of Persoonieae, nectaries are initiated from a broadened receptacle in alternistamenous sites after zonal growth beneath and between the tepals and stamens has begun. The nectaries are interpreted as secondary organs, not reduced homologues of a “lost” petal or stamen series. Developmental variation is present among the examined taxa in several forms including the development of a Vorlaüferspitze (spine) on the upper portion of the tepals, adnation between the anthers and tepals, and formation of the carpel. In Placospermum the early formation of the carpel cleft extends to the floral receptacle and in the other taxa, the carpel cleft is distinctly above the receptacle. Different developmental pathways result in similar mature morphologies of the carpel in Persoonia falcata and Placospermum coriaceum. Bellendena montana is unique relative to the other taxa in having free stamens, a punctate stigma, reduced (not lost) floral bracts, and the floral and bract primordia are initiated from a common meristem. This study provides a foundation for future studies of the developmental basis of floral diversity within Proteaceae.     

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.     

Exine Micromorphology of Orchidinae (Orchidoideae,Orchidaceae): Phylogenetic Constraints or Ecological Influences?

BACKGROUND AND AIMS: Pollen characters have been widely used in defining evolutionary trends in orchids. In recent years, information on pollination biology and phylogenetic patterns within Orchidinae has become available. Hence, the aim of the presented work is to re-evaluate exine micromorphology of Orchidinae in light of recent phylogenetic studies and to test whether pollen micromorphology strictly depends on phylogenetic relationships among species or whether it is influenced by the marked differences in pollination ecology also reported among closely related species. METHODS: Pollen sculpturing of 45 species of Orchidinae and related taxa was investigated using scanning electron microscopy. To cover potential intraspecific variation, several accessions of the same species were examined. KEY RESULTS: Orchidinae show remarkable variation in exine sculpturing, with a different level of variation within species groups. In some genera, such as Serapias (rugulate) and Ophrys (psilate to verrucate), intrageneric uniformity corresponds well to a common pollination strategy and close relationships among species. However, little exine variability (psilate-scabrate and scabrate-rugulate) was also found in the genus Anacamptis in spite of striking differences in floral architecture and pollination strategies. A larger variety of exine conditions was found in genera Dactylorhiza (psilate, psilate-scabrate and reticulate) and Orchis s.s. (psilate, reticulate, perforate-rugulate and baculate) where no unequivocal correspondence can be found to either phylogenetic patterns or pollination strategies. CONCLUSIONS: Changes in pollen characteristics do not consistently reflect shifts in pollination strategy. A unique trend of exine evolution within Orchidinae is difficult to trace. However, the clades comprising Anacamptis, Neotinea, Ophrys and Serapias show psilate to rugulate or scabrate pollen, while that of the clade comprising Chamorchis, Dactylorhiza, Gymnadenia, Orchis s.s., Platanthera, Pseudorchis and Traunsteinera ranges from psilate to reticulate. Comparison of the data with exine micromorphology from members of the tribe Orchidieae and related tribes suggests a possible general trend from reticulate to psilate.     

Sirindhomia, a new orchid genus from Southeast Asia

The new orchid genus Sirindhomia , named after H. R. H. Princess Maha Chakri Sirindhorn of Thailand, is established to accommodate three species from Thailand (Chiang Mai and Tak provinces), Myanmar (Shan State), and China (Yunnan province). Two new species are described and a new combination, based on Habenaria monophylla Collett & Hemsl., is made; all of the three species are illustrated, and a distribution map is provided. Sirindhomia belongs to subtribe Orchidinae and has an overall similarity with Ponerorchis, Hemipilia , and Amitostigma. However, it significantly differs in its column morphology which is more reminiscent of that found in the vegetatively distinct genus Orchis. The new species, Sirindhomia pulchella and S. mirabilis , seem to be local endemics, as they are only known from the Thai mountains Doi Chiang Dao and Khao Hua Mot, respectively. Sirindhomia monophylla , on the other hand, is known from a very large part of the range of the genus. All Sirindhomia species known are restricted to limestone mountains at 800–2200 m alt., mainly growing in rock crevices and among scrub as well as on grassy slopes. They flower from April to June.     

Corona and anther skirt in Hoya (Apocynaceae, Marsdenieae)

The so called revolute margins of the corona in the genus Hoya (Marsdenieae) are homologous to the anther skirt. The anther skirt is primarily formed of two latero-basal lobes of the anther. In Hoya these lobes are fused with the underside of the basal process of the staminal corona and have evolved into a dominant structure of the gynostegium. Embedded in the anther skirt is the nectar tube, formed by the basal elongation of the guide rail. In many species, however, the function of nectar secretion for pollinator reward has been transferred to the anther skirt beneath the basal process of the corona. A survey of the Marsdenieae shows that the potential for developing an anther skirt is present in several other genera as well, though nowhere has it evolved into such elaborated structures as in Hoya.     

Developmental studies in orchid flowers IV: Cypripedioid species

The floral development of four species of Cypripediaceae (sensu Rasmussen 1985) was studied by means of scanning electron microscopy, with special attention to the early development of the organs that constitute the gynostemium. At the ventral base of the gynostemium a prominent structure was observed. It is most probably a vestige of the median adaxial stamen a₃ based on its early initiation and place of origin. In Cypripedium calceolus the median carpel primordium is, according to expectation, initiated slightly earlier than the lateral carpel primordia, and later develops into the largest stigma lobe. Interestingly, Cypripedium irapeanurn shows an opposite sequence in the initial phase of the carpel development in that the primordia of the lateral carpels are initiated before the primordium of the median carpel.     

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.     

Morphology and development of the reproductive shoots of Lilaea scilloides (Poir.) Hauman (Alismatidae)

Shoots of adult plants of Lilaea scilloides have a sympodial form. Each unit of the sympodium bears a single sheathing prophyll (which is the only kind of foliage leaf produced in the adult) and terminates in an inflorescence. The prophyll subtends the next unit of the sympodium. A further accessory bud can form in association with each unit. This bud repeats the pattern of the main sympodium, giving the plant a tufted habit. Five different kinds of flower can be identified in the inflorescence: a unisexual male flower with a single perianth member and adnate stamen; a bisexual flower, with a single perianth member and adnate stamen, and a single carpel with an anatropous bitegmic ovule; a unisexual female flower with a single perianth member and carpel; a unisexual female flower comprising only a single carpel; and a female flower comprising only a single carpel with a very long filamentous style. The first four kinds occur in the upper part of the inflorescence which is normally elevated on a scape, while the last kind is restricted to the base of the inflorescence. In the position of the basal flowers several variations have been observed in cultivated material. These include branching associated with the basal flowers, which results in the development of additional basal flowers or inflorescences, and even total replacement of a basal flower by an inflorescence or a branching structure bearing flowers. A review of past literature includes a clarification of some persistent errors which have confused the taxonomic position of the plant and the morphological interpretation of the reproductive appendages.     

FLORAL DEVELOPMENT IN GYMNOTHECA CHINENSIS (SAURURACEAE)

The development of the inflorescence and flowers are described for Gymnotheca chinensis Decaisne (Saururaceae), which is native only to southeast China. The inflorescence is a short terminal spike of about 50–70 flowers, each subtended by a small bract. There are no showy involucral bracts. The bracts are initiated before the flowers, in acropetal order. Flowers tend to be initiated in whorls of three which alternate with the previous whorl members. No perianth is present. The flower contains six stamens, and four carpels fused in an inferior ovary containing 40–60 ovules on four parietal placentae. Floral symmetry is dorsiventral from inception and throughout organ initiation. Floral organs are initiated in the following order: 1) median adaxial stamen, 2) a pair of lateral common primordia which bifurcate radially to produce two stamen primordia each, 3) median abaxial stamen, 4) a pair of lateral carpel primordia, 5) median adaxial carpel, 6) median abaxial carpel. This order of initiation differs from that of any other Saururaceae previously investigated. The inferior ovary results from intercalary growth below the level of stamen attachment; the style elongates by intercalary growth, and the four stigmas remain free. The floral structure of Gymnotheca is relatively advanced compared to Saururus, but its assemblage of specializations differs from that of either Anemopsis or Houttuynia, the other derived genera in the Saururaceae.     

台闽苣苔（苦苣苔科）花部器官的形态发生

在扫描电镜下对台闽苣苔 (T .oldhamii (Hemsl.)Solereder)进行了花部器官形态发生的观察 ,为探索该类群的个体发育、类群间的系统发育关系和进化趋势提供依据。研究发现该属植物萼片、花冠和雄蕊发生式样均为五数花类型 ,它们各自来源于花原基上分化出来的萼片原基、花冠原基和雄蕊原基 ;花冠与雄蕊的两侧对称性与花冠上唇生长稍快和退化雄蕊原基发育迟滞相关 ;萼片原基的发生和发育的顺序是不一致的 :萼片原基发生的式样为近轴中原基—远轴 2原基— 2侧原基 ,发育式样则为近轴中萼片— 2侧萼片—远轴 2萼片 ,花蕾时为镊合状排列。花冠裂片原基的发生和发育式样是一致的 ,即远轴中裂原基 (下唇中裂片 )—远轴 2侧裂原基 (下唇 2侧裂片 )—近轴 2裂原基 (上唇 2裂片 )。花蕾期卷迭式为覆瓦状排列 ,从外向内 :下唇中裂片—下唇 2侧裂片—上唇 2裂片或下唇 2侧裂片—上唇 2裂片—下唇中裂片。雄蕊原基与花冠裂片原基互生 ,前方雄蕊原基在发生上稍迟于后方雄蕊原基 ,后者与退化雄蕊原基几乎同时发生 ,但较小 ,并与近轴心皮 (或柱头上唇 )对生。将该属与玄参科 (Scrophulari aceae)的地黄属 (Rehmannia)、苦苣苔科 (Gesneriaceae)的异叶苣苔属 (Whytockia)和尖舌苣苔属 (Rhynchoglossum)的花部器官比较发现     

Molecular phylogenetics and evolutionary history of the neotropical Satyrine Subtribe Euptychiina (Nymphalidae: Satyrinae)

The Euptychiina is one of the more diverse lineages of satyrine butterflies, represented by over 300 species. The first phylogenetic analyses of the subtribe is presented based on 2506 aligned nucleotide sequences obtained from 69 individuals spanning 28 ingroup genera and nine outgroup genera. Two genes were used, the mitochondrial gene cytochrome oxidase 1 (1268 bp) and the nuclear gene elongation factor-1alpha (1238 bp). The subtribe is never recovered as monophyletic in analyses using parsimony, maximum likelihood, or Bayesian inference. Several euptychiine genera are placed basal to the ingroup, but support is found only for Euptychia and Oressinoma. Three main lineages within the ingroup were clearly defined and many taxonomic groupings within the clades strongly supported. The majority of genera tested were paraphyletic or polyphyletic. Based on results presented here and novel host use, a close relationship of Euptychia to the Indo-Australian tribe Ragadiini is hypothesized. Origins of the group remain unclear, but the basal position of most of the Nearctic genera is discussed.     

Carpels in Brasenia (Cabombaceae) are completely ascidiate despite a long stigmatic crest

BACKGROUND AND AIMS: The morphological structure of anthetic carpels of Brasenia (Cabombaceae), a member of the phylogenetically basal ANITA grade, has not been studied before. The carpel has a long stigmatic crest on the ventral side and could give the impression of a conduplicate structure. This is in contrast to the carpel structure in other genera of the ANITA grade. Therefore, a study of carpel development and carpel structure at anthesis was carried out. METHODS: Carpels of Brasenia schreberi were studied at different developmental stages up to anthesis by means of microtome section series and SEM to analyse and reconstruct the outer and inner carpel morphology. KEY RESULTS: Carpels of Brasenia are extremely ascidiate up to anthesis. The elongate stigma originates around the mouth of the young carpel, which is slightly curved toward the centre of the flower. Subsequently, the stigmatic zone below the mouth expands by massive intercalary elongation. CONCLUSIONS: In their ascidiate shape, carpels of Brasenia are similar to carpels of Cabomba, the other genus of Cabombaceae, which, in contrast, has a short stigma restricted to the tip of the carpel. Thus, the morphological structure is independent of the extent (and one-sidedness) of the stigma. The outer shape of carpels at anthesis does not allow the inference of the inner morphological surface. If an angiosperm carpel has a one-sided stigma it can be extremely conduplicate or extremely ascidiate. Therefore, caution has to be used in the interpretation of the structure of fossil carpels.     

Floral ontogeny of Lecointea, Zollernia, Exostyles, and Harleyodendron (Leguminosae: Papilionoideae: Swartzieae s.l)

Floral initiation and development were examined using scanning electron microscopy in Exostyles venusta, Harleyodendron unifoliolatum, Lecointea hatschbachii, and Zollernia ilicifolia. Common features include (1) unidirectional sepal initiation, (2) simultaneous petal initiation, (3) unidirectional initiation of each stamen whorl (except in the antesepalous whorl in Lecointea and Exostyles), (4) overlap in time of initiation of the two stamen whorls, and (5) initiation of the carpel concurrently with petals. Significant developmental features include (1) the first sepal median abaxial in all except Lecointea where it is non-median abaxial; (2) intraspecific variation in petal aestivation in Exostyles, Harleyodendron, and Lecointea; (3) initiation of antepetalous stamens before the antesepalous ones in Zollernia, Exostyles, and Lecointea; and (4) ovule initiation before the carpel margins are fused in Exostyles. The stamen sequence has not been found in any other legumes. The following late developmental events distinguish the four genera from each other: copious hairs hold the anthers together as a domelike structure at anthesis in Harleyodendron; zygomorphy in Zollernia results from differing petal reflexion; late hypanthium in Exostyles, Lecointea, and Holocalyx (no hypanthium in Harleyodendron or Zollernia); and reflexed sepal lobes in Exostyles, Harleyodendron, and Zollernia but not in Holocalyx and Lecointea. The genera studied here are ontogenetically more similar to taxa of Sophoreae than to other Swartzieae that have been investigated. None of the taxa studied here has a ring meristem, the structure that characterizes the remaining swartzioid taxa studied elsewhere.     

Floral organogenesis of Potamogeton distinctus A. Benn. (Potamogetonaceae)

The floral organogenesis of Potamogeton distinctus A. Benn. was observed under the scanning electron microscope (SEM). The floral buds are first initiated on the lower portion of inflorescence in alternating whorls of three. Each of the floral buds is subtended by a bract primordium during the early stages. The primordia of the floral appendages arise on the floral bud acropetally. Two lateral tepals are first initiated and then two median ones soon after. Stamens are normally initiated as elongate primordia opposite the tepals, with the two lateral stamens preceding the median ones. The two carpel primordia arise alternating with the stamens. In some flowers, one of the two gynoecial primordia becomes inactive soon after they are initiated, or only one carpel primordium is initiated. The present observation of the gynoecial development supports the viewpoint that the evolution of flower in Potamogeton involves a reduction in number of parts. The existence of bract primordium during the early stages in many species of Potamogeton indicates that the absence of bractin mature flowers should be the result of reduction.