Scanning Electron Microscopic Studies on the Organ Development of

The pattern of development of the floral parts of Longan flower was followed using scanning electron microscope. Floral initiation begins with the formation of calyx protrusions around the floral apex. After the calyx protrusions have appeared, the petal primordia at the base of the floral apex start to appear and then followed by the androecium primordia which appear at the periphery of the floral apex. Gynoecium formation begins much later (at about 30 days after floral initiation). In the male flower, androecium develops normally forming anthers and filaments. Anthers also develop in the female flowers but they are smaller and the filaments much shorter. Gynoecium in the female flower is well developed and when mature it produces a long style, a two-prong-stigma and two ovaries. In the male flower the gynoecium is poorly developed the style is short and the stigma seldom splits. Ovaries are also poorly developed in the male flower. In addition to male and female flowers, Longan also forms a number of abnormal flowers with poorly developed androecium and gyn6ecium. Male and female flowers only become apparent at about 40 days after the initiation of flower differentiation. Prior to this it is difficult to know whether a particular developing flower is going ultimately to become a male or female flower. The formation of abnormal flowers also become obvious' at about 40 days after the initiation of flower differentation.     

Anatomy and ontogeny of unisexual flowers in dioecious Woonyoungia septentrionalis （Dandy） Law （Magnoliaceae）

Woonyoungia septentrionalis （Dandy） Law is aceae. The floral morphology and structure of the species a dioecious species with unisexual flowers in Magnoliare conspicuously different from other species and are important to the study of floral phylogeny in this family. The floral anatomy and ontogeny were investigated to evaluate the systematic position of W. septentrionalis, using scanning electron microscopy and light microscopy. All of the floral organs are initiated acropetally and spirally. The carpels are of conduplicated type without the differentiation of stigma and style. The degenerated stamens in the female flowers have the same structures as the normal stamens at the earlier developmental stages, but they do not undergo successive development and eventually degenerate. The male floral apex was observed to have the remnants of carpels in a few investigated samples. As the bisexual flower features could be traced both in the male and female flowers in W. septentrionalis, it suggests that the flower sex in Magnoliaceae tends toward unisexual. As well as the unisexual flowers, the reduced tepals and carpels and concrescence of carpels conform to the specialized tendency in Magnoliaceae, which confirms the derived position of W. septentrionalis in this family. As the initiation pattern of floral parts of W. septentrionalis is very similar to other species in this family, it needs further investigation and especially comparison with species in Kmeria to evaluate the separation of Woonyoungia.     

A SCANNING ELECTRON MICROSCOPIC STUDY ON THE INITIATION AND DEVELOPMENT OF FLORAL ORGANS OF BRASSICA NAPUS (CV. WESTAR)

The initiation and development of the floral organs of Brassica napus L. (cv. Westar) were examined using the scanning electron microscope. After transition of the vegetative apex into an inflorescence apex, flower primordia were initiated in a helical phyllotactic pattern. The sequence of initiation of the floral organs in a flower bud was that of sepals, stamens, petals and gynoecium. Of the four sepal primordia, the abaxial was initiated first, followed by the two lateral and finally the adaxial primordium. The four long stamens were initiated simultaneously in positions alternating with the sepals. The two short stamens were initiated basipetal to and outside the long stamens, and opposite the lateral sepals. The petals arose on either side of the two short stamens and the gynoecium was produced from the remainder of the apex. During development, the sepal primordia curved sharply at the tips and tightly enclosed the other organs. Stamen primordia developed tetralobed anthers at an early stage while filament elongation occurred just prior to anthesis. A unique pattern of bulbous cells was present on the abaxial surface of the anther. Growth of petal primordia lagged relative to the other floral organs but expansion was rapid prior to anthesis. The gynoecium primordium was characterized by an invagination early in development. At maturity, there was differentiation of a papillate stigma, an elongated style and a long ovary marked externally by sutures and divided internally by a septum. Distinct patterns of cuticular thickenings were observed on the abaxial and adaxial surfaces of the petals and stamens and on the surface of the style. The patterns were less obvious on the sepals and ovary. Stomata were present on both surfaces of the mature sepals, on the style and restricted areas on the abaxial surface of the anthers and nectaries but were absent from the petals, the adaxial surface of the stamens and the ovary. No hairs were present on any of the floral organs.     

Floral morphogenesis in Sinofranchetia (Lardizabalaceae) and its systematic significance

The floral organs of Sinofranchetia chinensis Hemsl. (Lardizabalaceae) are all spiral in initiation. Stamen and petal (nectar‐leaf) primordia initiate independently and are different in shape. The petals and three stamens in the first whorl are retarded in the early developmental stages. The carpel primordia are conduplicate; the stigma is formed around the upper part of the ventral slit and the style is not differentiated. The functionally unisexual flowers are bisexual in organization in the early developmental stages. The development of the flowers on the inflorescence is spiral and centripetal. Some floral characteristics of Sinofranchetia appear to be plesiomorphic in Lardizabalaceae. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 82–92.     

The arrest of development of abortive reproductive organs in the unisexual flower of<Emphasis Type="Italic"> Vitis vinifera</Emphasis> ssp.<Emphasis Type="Italic"> silvestris</Emphasis>

During the first stages of development, flowers of most dioecious species are hermaphroditic, with their transition to unisexual flowers being the result of the developmental arrest of one set of reproductive organs. In this work, we describe the development of male and female flowers of the dioecious wild grape species Vitis vinifera ssp. silvestris through scanning electron microscopy analysis and cytological observations, focusing our attention on the transition from bisexual to unisexual development. We divide floral development of the wild grape into eight stages. Differences between male and female flowers appear first at stage 6, when the style and stigma start to differentiate in female but not in male flowers. Cytological analysis of the slowly growing abortive pistil of male flowers shows that megagametophyte formation is, surprisingly, not inhibited. Instead of pistil abortion in the male flower, sexual determination is accomplished through programmed death of external nucellus cells and some layers of integumentary cells. Sterility of male structures in female flowers follows a different pattern, with microspore abnormalities evident from the time of their release from the tetrad. Sterile microspores and pollen grains in female flowers display an abnormal round shape, lacking colpi and possessing uniformly thickened cell walls that impede germination.     

MORPHOLOGY AND DEVELOPMENT OF THE FLOWERS OF BOOTTIA CORDATA,OTTELIA ALISMOIDES,AND THEIR SYNTHETIC HYBRID (HYDROCHARITACEAE)

The inferior ovary of Boottia cordata, Ottelia alismoides, and their hybrid is appendicular in nature, the carpels are congenitally only slightly connate, and they are unsealed. All floral organs except the sepals originate from common primordia in the female and bisexual flowers. A flat residual floral apex is pressnt. There is a vestigial superior ovary of three ontogenetically fused carpels in the male flower of Boottia cordata. The hybrid is intermediate in many characteristics and has partially fertile stamens and staminodia. The sequence of development in all flowers is acropetal. These plants appear to be related to the Butomaceae and they show evolutionary tendencies parallel to those in the Nymphaeaceae.     

Floral and inflorescence morphology and ontogeny in Beta vulgaris, with special emphasis on the ovary position

Background and Aims

In spite of recent phylogenetic analyses for the Chenopodiaceae–Amaranthaceae complex, some morphological characters are not unambiguously interpreted, which raises homology questions. Therefore, ontogenetic investigations, emphasizing on ‘bracteoles’ in Atripliceae and flowers in Chenopodioideae, were conducted. This first paper presents original ontogenetic observations in Beta vulgaris, which was chosen as a reference species for further comparative investigation because of its unclarified phylogenetic position and its flowers with a (semi-)inferior ovary, whereas all other Chenopodiaceae–Amaranthaceae have hypogynous flowers.

Methods

Inflorescences and flowers were examined using scanning electron microscopy and light microscopy.

Key Results

Floral development starts from an inflorescence unit primordium subtended by a lateral bract. This primordium develops into a determinate axis on which two opposite lateral flowers originate, each subtended by a bracteole. On a flower primordium, first five tepal primordia appear, followed by five opposite stamen primordia. Simultaneously, a convex floral apex appears, which differentiates into an annular ovary primordium with three stigma primordia, surrounding a central, single ovule. A floral tube, which raises the outer floral whorls, envelops the ovary, resulting in a semi-inferior ovary at mature stage. Similarly, a stamen tube is formed, raising the insertion points of the stamens, and forming a staminal ring, which does not contain stomata. During floral development, the calyces of the terminal flower and of one of the lateral flowers often fuse, forming a compound fruit structure.

Conclusions

In Beta vulgaris, the inflorescence is compound, consisting of an indeterminate main axis with many elementary dichasia as inflorescence units, of which the terminal flower and one lateral flower fuse at a later stage. Floral parts develop starting from the outer whorl towards the gynoecium. Because of the formation of an epigynous hypanthium, the ovary becomes semi-inferior in the course of floral development.Key words: Beta vulgaris, Chenopodiaceae, floral ontogeny, gynoecial development, epigynous hypanthium, semi-inferior ovary, inflorescence ontogeny, LM, SEM     

极度濒危树种羊角槭花部形态特征及开花动态

以天目山自然保护区人工栽培的濒危树种羊角槭（Acer yangjuechi Fang et P.L.Chiu）为研究对象,于花期观察了花部形态特征、单株与群体水平开花动态,分析开花与结实的关系,结果表明：1.羊角槭花杂性、顶生花序着生有雄花和两性花,两性花多位于花轴顶端,雄花位于侧生轴顶端或下部,花序雄花与两性花数量比为三角槭的2.6倍,羊角槭枝条两性花偏少;2.观察到两种形态雄花,Ⅰ型雄花子房微型、柱头极度短缩呈黑点状、花盘较平,Ⅱ型雄花子房退化成一团白色绒毛,2裂柱头隐现,花盘较厚、辐射状凹裂;两性花子房成扁球状突出,柱头显著伸出,花丝长度短于雄花;3.单株两性花早于雄花开放,两性花集中于3日以内开放,呈集中开放模式,而对应此时同株上只有极个别雄花（7%以下）处于散粉阶段;4.群体两性花开放时期略早于雄花,二者间存在相对的间隔期。由此对羊角槭开花与种胚发育影响因素进行了探讨。     

Floral morphology and anatomy of Pittosporum tobira (Pittosporaceae)

Comparative studies are made on floral morphology and anatomy of female and male flowers of Pittosporum tobira. The two types of flower differ little from each other in structure at the early stage of floral development, but appear dimorphic towards anthesis. The male flower becomes cryptically bisexual, although its pistil is slender compared to that of the female flower. The stigmas of the male flower are receptive and can induce pollen germination. The structure of the style in the male flower is identical to that in the female flower. Ovules are produced on the protruded parietal placenta in the male flower, but their development is arrested at the stage of the 4–nucleate embryo sac. The female flower is clearly unisexual, with obviously aborted and sagittate anthers. Its pistil is rather plump and can produce darkish red seeds immersed in sticky pulp. The male and female flowers are similar in vascular anatomy. A conspicuous difference between the two types of flower lies in the stamens. Variation of sexual organs in the genus Pittosporum is reviewed. We assume that the flowers of Pittosporum are derived from the hermaphrodite-flowered ancestor and the female flower has become unisexual through partial reduction of sexual organs at a faster rate than the male flower.     

Correlation between development of female flower buds and expression of the CS-ACS2 gene in cucumber plants

Ethylene plays a key role in sex determination of cucumber flowers. Gynoecious cucumber shoots produce more ethylene than monoecious shoots. Because monoecious cucumbers produce both male and female flower buds in the shoot apex and because the relative proportions of male and female flowers vary due to growing conditions, the question arises as to whether the regulation of ethylene biosynthesis in each flower bud determines the sex of the flower. Therefore, the expression of a 1-aminocyclopropane-1-carboxylic acid synthase gene, CS-ACS2, was examined in cucumber flower buds at different stages of development. The results revealed that CS-ACS2 mRNA began to accumulate just beneath the pistil primordia of flower buds at the bisexual stage, but was not detected prior to the formation of the pistil primordia. In buds determined to develop as female flowers, CS-ACS2 mRNA continued to accumulate in the central region of the developing ovary where ovules and placenta form. In gynoecious cucumber plants that produce only female flowers, accumulation of CS-ACS2 mRNA was detected in all flower buds at the bisexual stage and at later developmental stages. In monoecious cucumber, flower buds situated on some nodes accumulated CS-ACS2 mRNA, but others did not. The proportion of male and female flowers in monoecious cucumbers varied depending on the growth conditions, but was correlated with changes in accumulation of CS-ACS2 mRNA in flower buds. These results demonstrate that CS-ACS2-mediated biosynthesis of ethylene in individual flower buds is associated with the differentiation and development of female flowers.     

新疆胡颓子属植物花部性状的变异及其分类学价值

新疆胡颓子属植物栽培历史久、变异丰富、种下变异类型多、分类较为困难,因此有必要进一步发掘该属落叶组植物的分类学特征,尤其是对相对保守的繁殖器官的性状进行筛选。该研究以形态较为稳定的繁殖器官为切入点,分析花部性状的变异特点,筛选稳定性状,以期为解决该属的分类难题提供依据。先采用定株采集和同花标记的方法,对比分析了柱头形态、花盘先端有毛无毛、花柱与雄蕊的长短比、花被裂片程度四个性状的稳定性。结果表明:花盘先端有毛无毛、花柱与雄蕊的长短比、花被裂片程度三个性状较稳定,可以作为分类依据;柱头形态在单花中表现稳定,但在单株中出现极大的变异,不具有分类价值;然后采取新疆南、北疆地区的胡颓子属落叶组的尖果沙枣、大果沙枣和沙枣这三种来验证花部性状的稳定性,证明了上述结论的正确性,同时也是对该属分类研究实践的应用。该结果可为胡颓子属的经典分类学和形态学研究以及植物的开发和利用等提供参考依据。     

臭椿花器官分化的初步研究

利用扫描电镜(SEM)和光镜(LM)对臭椿花序及花器官的分化和发育进行了初步研究,表明:1)臭椿花器官分化于当年的4月初,为圆锥花序;2)分化顺序为花萼原基、花冠原基、雄蕊原基和雌蕊原基。5个萼片原基的发生不同步,并且呈螺旋状发生;5个花瓣原基几乎同步发生且其生长要比雄蕊原基缓慢;雄蕊10枚,两轮排列,每轮5个原基的分化基本是同步的;雌蕊5,其分化速度较快;3)在两性花植株中,5个心皮顶端粘合形成柱头和花柱,而在雄株中,5个心皮退化,只有雄蕊原基分化出花药和花丝。本研究着重观察了臭椿中雄花及两性花发育的过程中两性花向单性花的转变。结果表明,臭椿两性花及单性花的形成在花器官的各原基上是一致的(尽管时间上有差异),雌雄蕊原基同时出现在每一个花器官分化过程中,但是,可育性结构部分的形成取决于其原基是否分化成所应有的结构:雄蕊原基分化形成花药与花丝,雌蕊原基分化形成花柱、柱头和子房。臭椿单性花的形成是由于两性花中雌蕊原基的退化所造成,其机理有待于进一步研究。     

Developmental morphology of the flower of <Emphasis Type="Italic">Dracontium polyphyllum</Emphasis> in the context of the phylogeny of the Araceae

The inflorescence of Dracontium polyphyllum consists of 150 – 300 flowers arranged in recognisable spirals. The flower has 5 – 6 (90% of observed specimens), or 7 broad tepals enclosing 9 – 12 stamens (occasionally 7) inserted in two whorls. The gynoecium is trilocular (90% of observed specimens) or tetralocular. The tetralocular gynoecia are found at random among the trilocular gynoecia. Each locule encloses an ovule inserted in an axile position, in the median portion of the ovary. Each carpel has its own stylar canal. However, in the upper portion of the style, there is only one common stylar canal. Floral organs are initiated in an acropetal direction in the following sequence: tepals, stamens, and carpels. During later stages of development, the tepals progressively cover the other floral organs. The first floral primordia are initiated on the upper portion of the inflorescence. During early stages of development, the floral primordia have a circular shape. The tepals are initiated nearly simultaneously. During later stages of development, the first whorl of stamens develops in alternation with the tepals and is followed by a second whorl of stamens. The trilocular or tetralocular nature of the ovary is clearly visible during early stages of development of the gynoecium. Recent molecular studies show that Anaphyllopsis A. Hay and Dracontium L. are closely related. However, although pentamerous flowers have been observed in Anaphyllopsis, the developmental morphology of the flower of Dracontium is different from that of Anaphyllopsis.     

Floral development of Phyllanthus chekiangensis (Phyllanthaceae), with special reference to androecium and gynoecium

The floral development of Phyllanthus chekiangensis has been studied by scanning electron microscopy. The perianth organs are initiated in two whorls, dimerous in male flowers and trimerous in female flowers, with a longer plastochron between whorls than between the organs within a whorl. Male flowers have two stamens. The prominent connective protrusions begin development simultaneously with the floral disk. The disk is two-lobed in male flowers but continuous in female flowers. In female flowers, the developing gynoecium remains open relatively long, so the developing ovules are visible from the outside for some time. The direction of the hemitropous ovules in the carpels is antitropous (epitropous). Two small obturators are formed per carpel, one above each ovule. The prominent nucellar beak extends far beyond the “micropyle”. A micropyle in the classical sense formed by integuments closing over the nucellus apex is not present at any stage of development. Thus, it is not correct to say that the nucellar beak “grows through the micropyle”. The exposed nucellar beak continues the curvature of the antitropous (epitropous) ovule and becomes contiguous with the obturator. The unusual length of the nucellar beak may be a potential synapomorphy of the enlarged Phyllanthus clade as inferred from molecular phylogenetics.     

Developmental analyses reveal early arrests of the spore-bearing parts of reproductive organs in unisexual flowers of cucumber (<Emphasis Type="Italic">Cucumis sativus</Emphasis> L.)

To understand the regulatory mechanisms governing unisexual flower development in cucumber, we conducted a systematic morphogenetic analysis of male and female flower development, examined the dynamic changes in expression of the C-class floral organ identity gene CUM1, and assessed the extent of DNA damage in inappropriate carpels of male flowers. Accordingly, based on the occurrence of distinct morphological events, we divided the floral development into 12 stages ranging from floral meristem initiation to anthesis. As a result of our investigation we found that the arrest of stamen development in female flowers, which occurs just after the differentiation between the anther and filament, is mainly restricted to the primordial anther, and that it is coincident with down-regulation of CUM1 gene expression. In contrast, the arrest of carpel development in the male flowers occurs prior to the differentiation between the stigma and ovary, given that no indication of ovary differentiation was observed even though CUM1 gene expression remained detectable throughout the development of the stigma-like structures. Although the male and female reproductive organs have distinctive characteristics in terms of organ differentiation, there are two common features regarding organ arrest. The first is that the arrest of the inappropriate organ does not affect the entirety of the organ uniformly but occurs only in portions of the organs. The second feature is that all the arrested portions in both reproductive organs are spore-bearing parts.Abbreviations SEM Scanning electron microscopy - TEM Transmission electron microscopy - TUNEL TdT-mediated dUTP nick-end labeling     

DEVELOPMENT AND VASCULATURE OF THE FLOWERS OF LOPHOTOCARPUS CALYCINUS AND SAGITTARIA LATIFOLIA (ALISMACEAE)

The development of the bisexual flower of Lophotocarpus calycinus and of the unisexual flowers of Sagittaria latifolia has been observed. In all eases floral organs arise in acropetal succession. In L. calycinus, after initiation of the perianth, the first whorl of stamens to form consists of six stamens and is ordinarily followed by two alternating whorls of six stamens each. The very numerous carpels arc initiated spirally. In the male flower of S. latifolia the androecium develops in spiral order. A few rudimentary carpels appear near the floral apex after initiation of the stamens. There are no staminodia. The female flower has a similar developmental pattern to that of Lophotocarpus except that a prominent residual floral apex is left bare of carpels. The vascular system in all flowers is semiopen, with vascular bundles passing to the floral organs in a pattern unrelated to the relative positions of those organs. The androecia of these two taxa are similar to those of some Butomaceae and relationships based on ontogeny and morphology are suggested. The gynoecia are meristically less specialized but morphologically more specialized than the gynoecia of Butomaceae.     

马桑绣球(绣球科)的花器官发生和发育

在扫描电镜下观察了马桑绣球Hydrangea aspera孕性花的发生及发育过程。马桑绣球的花器官向心轮状发生：花萼原基以2/5螺旋式相继发生,花瓣原基几乎同步发生。花瓣开始发育时,与花萼相对的雄蕊发生。与花瓣相对的雄蕊原基与心皮原基几乎同时出现。初始心皮向上扩展,分化出花柱和柱头,向下延伸,嵌入花托,发育为下位子房。花发育成熟时,隔膜于子房的下部连续,而中部和上部不连续,即子房为不完全2室。经过与绣球属已观察过的另外5种1亚种花器官发生和发育比较,发现马桑绣球与藤绣球H. ano mala subs     

FLORAL DEVELOPMENT OF POTAMOGETON RICHARDSONII

The inception and development of the sterile floral appendages of Potamogeton richardsonii have been re-investigated with a refined dissection technique (Sattler, 1968) and improved microtechnical methods (Feder and O'Brien, 1968). The results obtained by Sattler (1965) are confirmed, i.e., the sterile appendages are initiated at the flanks of the floral apex before the stamen primordia are formed. Consequently, they may be homologized with tepals or perianth members, although in the mature flower they are inserted at the stamen connective, due to growth between and at the base of each developing tepal and stamen. Each carpel arises as a radial primordium which becomes peltate immediately after its inception. One ovule primordium is initiated at the cross-zone. The stigma becomes bilobed. A slight outgrowth develops at the abaxial side of the style. The floral apex has a two-layered tunica. The primordia of the tepals, carpels, and ovules arise by periclinal divisions in the second tunica layer, whereas the stamen primordia are initiated by periclinal divisions in the corpus and second tunica layer. Variation in floral pattern, especially with regard to the number of appendages, has been observed in flowers near the tip of the inflorescence axis.     

In vitro culture of young floral buds of tomato (Lycopersicon esculentum mill.)

Young floral buds of tomato (Lycopersicon esculentum Mill.), with sepal primordia only, were cultured successfully in a liquid medium containing Murashige and Skoog's salts, White's vitamins and glycine, 3% (w/v) sucrose and benzylaminopurine (BAP). In 5 weeks, 60–70% of the cultured buds showed normal flower development through to anthesis, and a full complement of floral organs was produced. In the anthers, microsporogenesis occured and microspores and pollen grains were formed. The gynoecium was differentiated into an ovary, style and a stigma, and the ovary contained many ovules, some of which had developing embryo sacs. The floral organs grown in vitro were, however, smaller in size than those produced in vivo. In the control medium, i.e. without BAP, the floral buds produced petal and stamen primordia only and they too showed limited growth. The data presented shows the importance of cytokinins in the initiation and development of organs in the excised floral buds.