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.     

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.     

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.     

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.     

Studies in the Lauraceae: V. Comparative Morphology of The Flower

The morphological nature of the various parts of the lauraceousflower has been discussed on the basis of available evidencefrom floral anatomy and ontogeny. Evidence from floral anatomysupports the view that both whorls of perianth are homologousand that the inner whorl does not represent modified stamens.The perianth has not attained a level of differentiation intosepals and petals in a real sense. The lauraceous flower mighthave had staminal appendages in all the four whorls in the ancestralcondition. The living genera represent varying degrees of reduction.These appendages are regarded as modified stamens. The stamensin the family cannot be considered as reduced branch systems.The androecium is interpreted as consisting of stamen fascicles.The two-trace carpel is common in the family. Evidence fromontogeny and vascular anatomy makes it improbable that the gynoeciumconsists of more than one carpel. The carpel is essentiallyof the conduplicate type.     

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。     

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.     

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 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.     

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.     

Roles of synorganisation,zygomorphy and heterotopy in floral evolution: the gynostemium and labellum of orchids and other lilioid monocots

A gynostemium, comprising stamen filaments adnate to a syncarpous style, occurs in only threc groups of monocots: the large family Orchidaceae (Asparagales) and two small genera Pauridia (Hypoxidaceae: Asparagales) and Corsia (Corsiaceae, probably in Liliales), all epigynous taxa. Pauridia has actinomorphic (polysymmetric) flowers, whereas those of Corsia and most orchids are strongly zygomorphic (monosymmetric) with a well-differentiated labellum. In Corsia the labellum is formed from the outer median tepal (sepal), whereas in orchids it is formed from the inner median tepal (petal) and is developmentally adaxial (but positionally abaxial in orchids with resupinate flowers). Furthermore, in orchids zygomorphy is also expressed in the stamen whorls, in contrast to Corsia. In Pauridia a complete stamen whorl is suppressed, but the 'lost' outer whorl is fused to the style. The evolution of adnation and zygomorphy are discussed in the context of the existing phylogenetic framework in monocotyledons. An arguably typological classification of floral terata is presented, focusing on three contrasting modes each of peloria and pseudopeloria. Dynamic evolutionary transitions in floral morphology are assigned to recently revised concepts of heterotopy (including homeosis) and heterochrony, seeking patterns that delimit developmental constraints and allow inferences regarding underlying genetic controls. Current evidence suggests that lateral heterotopy is more frequent than acropetal heterotopy, and that full basipetal heterotopy does not occur. Pseudopeloria is more likely to generate a radically altered yet functional perianth, but is also more likely to cause acropetal modification of the gynostemium. These comparisons indicate that there are at least two key genes or sets of genes controlling adnation, adaxial stamen suppression and labellum development in lilioid monocots; at least one is responsible for stamen adnation to the style (i.e. gynostemium formation), and another controls adaxial stamen suppression and adaxial labellum formation in orchids. Stamen adnation to the style may be a product of over-expression of the genes related to epigyny (i.e. a form of hyper-epigyny). If, as seems likely, stamen-style adnation preceded zygomorphy in orchid evolution, then the flowers of Pauridia may closely resemble those of the immediate ancestors of Orchidaceae, although existing molecular phylogenetic data indicate that a sister-group relationship is unlikely. The initial radiation in Orchidaceae can be attributed to the combination of hyper-epigyny, zygomorphy and resupination, but later radiations at lower taxonomic levels that generated the remarkable species richness of subfamilies Orchidoideae and Epidendroideae are more likely to reflect more subtle innovations that directly influence pollinator specificity, such as the development of stalked pollinaria and heavily marked and/or spur-bearing labella.     

Pollinators,floral morphology and scent chemistry in the southern African orchid genus Schizochilus

Floral evolution often involves suites of traits, including morphology, colour and scent, but these traits are seldom analysed together in comparative studies. We investigated the associations between floral traits and pollination systems in Schizochilus, a southern African orchid genus with small nectar-producing flowers that has not been studied previously with respect to pollination biology. Field observations indicated the presence of distinct pollination systems in the four species which occur in the Drakensberg, including pollination by muscid flies in Schizochilus angustifolius, tachinid flies in Schizochilus zeyheri, various small flies in Schizochilus bulbinella and bees and wasps in Schizochilus flexuosus. Pollination success and pollen transfer efficiency clearly differed among the four species but were not correlated with the quantity of nectar rewards. Multivariate analysis of floral morphology and floral scent chemistry based on GC-MS data revealed significant differences among species as well as populations within species. The floral scent of S. angustifolius was dominated by the benzenoid compounds benzaldehyde and phenylacetaldehyde. Samples of one population of S. bulbinella were relatively similar to S. angustifolius but samples of another population were very distinct due to the occurrence of the nitrogen-containing compounds 3-methyl-butyl aldoxime (syn/anti) and the higher amounts of aliphatic esters, alcohols and acids. In contrast, the floral scent of S. flexuosus and S. zeyheri was characterized by high relative amounts of methyl benzoate. We conclude that Schizochilus has distinct, specialized pollination systems associated with subtle but significant variation in floral morphology and scent chemistry. We also caution that sampling of several populations may be required to characterize floral scent composition at the species-level in plants.     

Feeding appendages of the Euphausiacea (Crustacea)

The Euphausiacea comprises about 85 species and the structure of the feeding appendages of 68 of these species is discussed here. A considerable uniformity is apparent in the appendages throughout the order but generic, and even in some cases, specific differences are evident. It is concluded from the study of the morphology of the appendages and the analyses of stomach contents that the majority of species in the genera Bentheuphwsia, Thysanopoda, Meganyctiphanes, Nyctiphanes, Pseudeuphausia, Euphausia, Tessara-brachion and Thysanoessa are omnivorous; that is, they can feed by filtering material from the water and act as predators of small zooplankton, especially copepods. Species in the genera Nematoscelis, Nematobrachion and Stylocheiron can feed on bottom deposits and also by predation of zooplankton but the amount of filter-feeding which they do may be limited because their mouthparts are not so well adapted for filtering as those of the previous group of genera.
It is suggested, from the study of the appendages and several other features of the animals, that the genera Thysanopoda, Meganyctiphanes, and Euphausia are closely related to one another and that a similar relationship exists between the genera Nematoscelis, Nematobrachion and Stylocherion. The genera Nyctiphanes and Pseudeuphausia are probably more closely related to the Thysanopoda group of genera and the genera Tessarabrachion and Thysanoessa to the Nematoscelis group of genera.     

The gynostemium of Bulbophyllum ecornutum (J. J. Smith) J. J. Smith (Orchidaceae)

RASMUSSEN, F. N., 1985. The gynostemium of Bulbophyllum ecornutum (J. J. Smith) J.J. Smith (Orchidaceae) . Stages in the development of the gynostemium of Bulbophyllum ecornutum demonstrate that the pollinium stalk is a hamulus in this and in a closely related species, B. gibbolabium . A hamulus arises by apical growth and reflexion of the median carpel. Hamuli have recently been discovered in several orchid genera, and a transverse fold of the rostellar apex is already known from a large group of orchids. The closely related B. cornutum has a quite different gynostemium structure.     

Floral development of Iris decora Wall. (Iridaceae)

The outer tepal and stamen primordia arise as secondary primordia on the outer tepal-stamenprimordia, which are formed on the floral apex. The inner tepal primordia are formed directly on the floral apex. All the floral appendages are initiated in the second tunica layer and are homologous with regard to their origin and early development. A short perianth tube is formed as a result of intercalary growth in the common bases of the tepal primordia. The intercalary growth in the fused bases of the floral appendages elevates the peripheral zone. The floral apex thus appears as a shallow cup. Further intercalary growth results in the formation of an inferior ovary. The ovules are initiated as outgrowths on placental ridges from the lateral ovary wall, the trilocular appearance being the result of secondary cohesion of the parietal placentae.     

Madagasikaria (Malpighiaceae): a new genus from Madagascar with implications for floral evolution in Malpighiaceae

Madagasikaria andersonii is described here as a new genus and species of Malpighiaceae from Madagascar. The phylogenetic placement of Madagasikaria was estimated by using combined data from ndhF and trnL-F chloroplast sequences and phytochrome (PHYC) and ITS nuclear sequences. It forms a strongly supported clade with the Malagasy endemic genera Rhynchophora and Microsteira. Despite nearly identical floral morphology among species in this clade (here called the madagasikarioid clade), these genera are easily distinguishable on the basis of their fruits. The schizocarpic fruits of Madagasikaria have distinctive mericarps. Each mericarp has a lateral wing, which completely encircles the nut, and a peculiar dorsal wing, which folds over on itself. The morphology of this fruit suggests that the homology of the unusual wing in Rhynchophora is lateral in nature and represents a reduced wing similar to the lateral wing in Madagasikaria. Taxa in the madagasikarioid clade all appear to be morphologically androdioecious and functionally dioecious, producing both staminate and "bisexual" (i.e., functionally carpellate) individuals. This condition appears to be exceedingly rare in flowering plants and has important implications for floral evolution within Malpighiaceae. Neotropical Malpighiaceae are pollinated by specialized oil-collecting anthophorine bees of the tribe Centridini and exhibit highly conserved floral morphology despite tremendous diversity in fruit morphology and habit. These oil-collecting bees are absent from the paleotropics, where most members of the Malpighiaceae lack both the oil glands and the typical floral orientation crucial to pollination by neotropical oil-collecting bees. The madagasikarioids represent one shift from the neotropical pollination syndrome among Old World Malpighiaceae.     

The questionable affinities of Corsia (Corsiaceae): evidence from floral anatomy and pollen morphology

The floral anatomy and pollen morphology of Corsia are described in the context of its systematic relationships. Flowers of Corsia are epigynous, lack septal nectaries and possess a large labellum formed from the outer median tepal (sepal). The labellum is highly vascularized and has a prominent outgrowth (callus) that is apparently nectiiferous in some species of section Sessilis , although not in section Unguiculatis . The six fertile stamens are proximally fused to the style, forming a gynostemium. This combination of labellum and gynostemium is otherwise found only in Orchidaceae (Asparagales), but the orchid labellum is formed from the opposite median inner tepal, and is therefore not homologous with that of Corsia . The three genera of Corsiaceae ( Corsia , Arachnitis and Corsiopsis ) are markedly different in some respects; e.g. only Corsia has a gynostemium. However, they share a unique synapomorphy in the presence of a labellum formed from the outer median tepal (sepal). Corsia and Arachnitis are also similar in pollen sexine sculpturing. Among other putative relatives, the range of morphological similarities between Corsia and Campynemataceae (Liliales) tends to support recent preliminary inferences from molecular data that they are closely related, but a relationship with Thismia (Dioscoreales) cannot be discounted. Both Campynemataceae and Thismia share similarities with Corsia , including epigyny, absence of septal nectaries, presence of tepal nectaries, and pollen morphology. © 2002 Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 138 , 315–324.     

海韭菜的花器官发生

运用扫描电镜（SEM）观察了海韭菜（Triglochin maritimum）的花器官发生发育过程。结果表明：海韭菜花发育是典型的单子叶植物发生模式,即两轮花被片、两轮雄蕊和两轮心皮以三基数轮状交替发生,花器官是以向心向顶的方式发生的,未发现“花被片—雄蕊复合原基”。 发育后期雄蕊和与之对生的花被片之间的共同基部可能是相继向上居间生长的结果。花被片轮和雄蕊轮二者之间在发育位置、时间和速率上存在差异,内轮花被片原基和外轮雄蕊原基的不同发育时间和发育速度使得在成熟花中内轮花被片位于外轮雄蕊的内方。观察结果不支持水麦冬属植物的花是退化（或压缩）的花序侧分枝等假花的观点。     

The controversial origin of the abdominal appendage‐like processes in immature insects: Are they true segmental appendages or secondary outgrowths? (Arthropoda hexapoda)

In this article, I review the major characteristics of different types of appendage‐like processes that develop at the abdominal segments of many immature insects, and I discuss their controversial morphological value. The main question is whether the abdominal processes are derived from segmental appendages serially homologous to thoracic legs, or whether they are “secondary” outgrowths not homologous with true appendages. Morphological and embryological data, in particular, a comparison with the structure and development of the abdominal appendages in primitive apterygote hexapods, and data from developmental genetics, support the hypothesis of appendicular origin of many of the abdominal processes present in the juvenile stages of various pterygote orders. For example, the lateral processes, such as the tracheal gills in aquatic nymphs of exopterygote insects, are regarded as derived from lateral portions of appendage primordia, homologous with the abdominal styli of apterygotan insects; these processes correspond either to rudimentary telopodites or to coxal exites. The ventrolateral processes, such as the prolegs of different endopterygote insect larvae, appear to be derived from medial portions of the appendicular primordia; they correspond to coxal endites. These views lead to the rejection of Hinton's hypothesis (Hinton [1955] Trans R Entomol Soc Lond 106:455–545) according to which all the abdominal processes of insect larvae are secondary outgrowths not derived from true appendage anlagen. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.