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.     

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.     

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.     

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.     

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.     

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.     

On Diplandrorchis,a very primitive and phylogenetically significant new genus of Orchidaceae

Diplandrorchis is a very curious new orchid genus, containing only one species D. sinica S. C. Chen, found in Huan-ren County of Liaoning Province in northeastern China. It, as the genus name implies, has two fertile stamens, borne on the upper part of the column near the terminal stigma. One of them is opposite to the dorsal sepal, while the other to the median petal (lip). Thus, they represent two median stamens of both inner and outer whorls. This is quite unique in the whole family, including the diandrous group, in which the two stamens are opposite to the lateral petals and thus represent the lateral ones of the inner whorl. The flower is erect, with its pale greenish or whitish perianth nearly regular. Two lateral sepals are more or less oblique, showing some difference from the dorsal one, but the three petals, which are thinner and narrower, are very similar to each other. Neither rostellum nor any other appendages are found in its column, but a terminal stigma and two erect stamens. The pollinia are naked and granular, which, in almost all flowers examined, have naturally fallen out of their cells on to the stigma. Apparently, it is self-fertilised, as found in Tangtsinia and some other primitive orchids. Besides, this interesting orchid is a dwarf saprophyte, with its habit very similar to that of Neottia, another saprophytic genus assigned to the subtribe Neottiinae. The fact that the saprophytic orchids are largely found in the primitive subtribes, such as the Neottiinae, Limodorinae, Vanillinae and Pogoniinae, is worthy of special attention. Theoretically, the saprophytic plants must have developed from green-leaved plants. In the Orchidaceae, however, what ancestor are the most primitive saprophytes derived from ? This is indeed an interesting question closely related to the origin of the Orchidaceae. From the facts mentioned above, the present genus is a very primitive or relic one and of great phylogenetic interest. It is placed here as the most primitive member in the subtribe Neottiinae, although it is sharply distinct from the remaining generaof this subtribe. It may deserve a separate subtribe, but further study is needed.     

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.     

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.     

A comparative study of floral development inTrillium apetalon andT. kamtschaticum (Liliaceae)

Trillium apetalon Makino is unique amongTrillium in having apetalous flowers. Using scanning electron microscope, the early floral development was observed in comparison with that ofT. kamtschaticum Pallas ex Pursh having petalous flowers. Morphologically petal primordia closely resemble stamen primordia in their more or less narrow and radially symmetric shape and are clearly distinct from sepal primordia with broad bases. Early in floral development sepal primordia are first initiated and subsequently two whorls of three primordia each are formed in rapid sequence, the first three at the corners and the second three at the sides of the triangular floral apex. Based on comparison in position and early developmental processes of their primordia, petals and outer stamens ofTrillium kamtschaticum are equivalent to outer stamens and inner stamens ofT. apetalon. The replacement of petals by outer stamens apparently leads to the loss of petals inTrillium apetalon flowers. Such a replacement can be interpreted in terms of homeosis. The replacement of the petal whorl leads to the serial replacement of the subsequent whorls: outer stamens by inner stamens, and inner stamens by gynoecium inTrillium apetalon. The term ‘serial homeosis’ is introduced for this serial replacement.     

大戟科麻疯树属三种植物花器官发生

利用扫描电子显微镜观察了大戟科Euphorbiaceae麻疯树属Jatropha麻疯树J. curcas L.、佛肚树J. podagrica Hook.和棉叶麻疯树J. gossypifolia L.花器官发生。结果表明: 麻疯树、佛肚树和棉叶麻疯树花萼原基均为2/5型螺旋发生。在同一个种不同的花蕾中, 花萼的发生有两种顺序: 逆时针方向和顺时针方向。远轴面非正中位的1枚先发生。5枚花瓣原基几乎同时发生。雄花中雄蕊两轮, 外轮对瓣, 内轮对萼。研究的3种麻疯树属植物雄蕊发生方式有两种类型: 麻疯树亚属麻疯树的5枚外轮雄蕊先同时发生, 5枚内轮雄蕊后同时发生, 佛肚树亚属佛肚树和棉叶麻疯树雄蕊8-9枚, 排成两轮, 内外轮雄蕊同时发生。雌花的3枚心皮原基为同时发生。麻疯树属单性花, 雌花的子房膨大而雄蕊退化, 雄花的雄蕊正常发育, 子房缺失。根据雄蕊发生方式, 支持将麻疯树属分为麻疯树亚属subgen. Jatropha和佛肚树亚属subgen. Curcas。     

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.     

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.     

Floral ontogeny inMazus pumilus (Scrophulariaceae)

InMazus pumilus, all the floral appendages are initiated in acropetal sequence in the second cell layer (except stamens) of the floral primordium by periclinal divisions. The actinomorphic calyx tube is formed due to zonal growth. The zygomorphy in corolla is evident from the inception of petal primordia which arise sequentially as independent units in order of one anterior, a pair of anterio-lateral followed by a pair of posterio-lateral. Later these primordia exhibit differential growth because of which zygomorphy becomes more pronounced. The upper corolla tube is formed by interprimordial growth and lower corolla tube by zonal growth. Stamens are initiated in the third layer of the floral apex. Unlike sepals and petals, in the development of stamens (4) underlying cells of corpus also contribute. Posterior stamen is absent. The stamens become epipetalous because of interprimordial and zonal growth in the common region below the bases of petals as well as stamens. The two carpel primordia arise as crescent shaped structures which become continuous due to interprimordial growth. The ovary is formed by a ring of zonal meristem. The style develops later between stigma and ovary because of intercalary growth. The residual apex grows vertically along with the ovary and forms the septum of the ovary. All the floral appendages exhibit similar pattern of histogenesis and early growth suggesting thereby the appendicular nature of these appendages.     

商陆属植物的花器官发生

为进一步研究商陆科的系统位置提供花器官发生和发育的证据,在扫描电子显微镜下观察了商陆Phytolacca acinosa、多雄蕊商陆P. polyandra和垂序商陆P. americana的花器官发生.结果表明: 商陆属植物花被的发生均为2/5型螺旋发生.在同一个种不同的花蕾中,花被的发生有两种顺序:逆时针方向和顺时针方向.远轴侧非正中位的1枚先发生.雄蕊发生于环状分生组织.在单轮雄蕊的种中8-10枚雄蕊为近同时发生;两轮雄蕊的种8枚内轮雄蕊先发生,6-8枚外轮雄蕊随后发生,内轮雄蕊为同时发生,外轮雄蕊发生次序不规则.心皮原基也发生于环状分生组织,8-10枚心皮原基为同时发生.在后来的发育过程中,商陆的心皮发育成近离生心皮雌蕊;其他2种心皮侧壁联合发育成合生心皮雌蕊.对商陆属植物花器官发生的类型及发育形态学做了分析,结果支持商陆科在石竹目系统发育中处于原始地位的观点.     

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.     

FLORAL DEVELOPMENT IN MANGROVE RHIZOPHORACEAE

The flowers of mangrove Rhizophoraceae (tribe Rhizophoreae) are adapted to three different pollination mechanisms. Floral development of representative species of all four genera suggests that the ancestral flower of the tribe was unspecialized, with successively initiated whorls of separate sepals, petals, antisepalous stamens, and antipetalous stamens; at its inception, the gynoecium had a united, half-inferior ovary and separate stigmatic lobes. This developmental pattern is found in Rhizophora mangle (wind-pollinated) and Ceriops decandra (insect-pollinated). In Kandelia, all floral organs distal to the sepals are initiated simultaneously, and there has apparently been an evolutionary amplification in the number of stamens to about six times the number of petals. Explosive pollen release evolved independently in C. tagal and in Bruguiera. In the former, all stamens belong to one whorl and arise simultaneously upon a very weakly differentiated androecial ring primordium. In Bruguiera, the androecial ring is pronounced, and two whorls of stamens arise upon it; the primordia of the antisepalous whorl arise first but are closer to the center of the apex than the antipetalous stamen primordia. The antisepalous stamens bend toward and are enclosed by the petals early in development. In all genera, the inferior ovary develops by zonal growth of receptacular tissue; additional intercalary growth above the placenta occurs in Bruguiera. In general, floral specialization is accompanied by an increase in the width of the floral apex compared to the size of the primordia, increasing fusion of the stylar primordia, and decreasing prominence of the superior portion of the ovary. Apparent specializations of petal appendages for water storage, including the presence of sub-terminal hydathodes (previously unreported in any angiosperm), were found in two species in which flowers remain open during the day but were absent from two species normally pollinated at night or at dawn. Distinctive tribal characteristics that may aid in phylogenetic analysis include the mode of development of the inferior ovary; the aristate, bifid, usually fringed petals that individually enclose one or more stamens; the intrastaminal floral disc; and the initially subepidermal laticiferous cell layer in the sepals and ovary.     

Subsidiary-cell development in the Catasetinae (Orchidaceae) and related groups

Developmental studies of stomata in the tribes Cymbidieae, Maxillarieae and Gongoreae (Orchidaceae) demonstrate the presence of definite subsidiary cells in these groups of the Orchidaceae, contrary to recent reports that the Orchidaceae lack subsidiary cells. Fifteen species in these groups were studied developmentally and an additional 36 species were studied from mature leaves. In the Cymbidieae the subsidiary cells may be the lateral trapezoid cells derived from the lateral contact cells, or the subsidiary cells may be derivatives of the trapezoid cells. In the species of Maxillarieae and Gongoreae studied the subsidiary cells were derivatives of the trapezoid cells. The type of subsidiary cell development in these groups is essentially the same as has been found in other advanced groups of epidendroid orchids that have subsidiary cells.     

The ontogenetic basis for floral diversity in <Emphasis Type="Italic">Agonis</Emphasis>, <Emphasis Type="Italic">Leptospermum</Emphasis> and <Emphasis Type="Italic">Kunzea</Emphasis> (Myrtaceae)

Floral development in three species each of Leptospermum and Kunzea, and one species of Agonis, is described and compared. Differences in the number of stamens and their arrangement in the flower at anthesis are determined by the growth dynamics of the bud. In Leptospermum, early expansion of the bud is predominantly in the axial direction and causes the stamen primordia to be initiated in antepetalous chevrons. In Kunzea, early expansion occurs predominantly in the lateral direction and successive iterations of stamen primordia are inserted alternately at more or less the same level. In both genera, further expansion in the lateral plane spreads the stamens into a ring around the hypanthium. Agonis flexuosa is similar to Leptospermum. Other variable factors include the timing at which stamen initiation commences (earlier in Leptospermum than Kunzea), the duration of stamen initiation (hence the total number of stamens produced – varies within genera), and very late differential expansion that forces stamens into secondary antesepalous groups in A. flexuosa and L. myrsinoides.The authors thank Dr H. Toelken for kindly providing some material and the impetus for this project. This research was supported by Australian Research Council grant AS19131815.     

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。