Floral development of petaloid Alismatales as an insight into the origin of the trimerous Bauplan in monocot flowers

Monocots are remarkably homogeneous in sharing a common trimerous pentacyclic floral Bauplan. A major factor affecting monocot evolution is the unique origin of the clade from basal angiosperms. The origin of the floral Bauplan of monocots remains controversial, as no immediate sister groups with similar structure can be identified among basal angiosperms, and there are several possibilities for an ancestral floral structure, including more complex flowers with higher stamen and carpel numbers, or strongly reduced flowers. Additionally, a stable Bauplan is only established beyond the divergence of Alismatales. Here, we observed the floral development of five members of the three ‘petaloid’ Alismatales families Butomaceae, Hydrocharitaceae, and Alismataceae. Outer stamen pairs can be recognized in mature flowers of Alismataceae and Butomaceae. Paired stamens always arise independently, and are either shifted opposite the sepals or close to the petals. The position of stamen pairs is related to the early development of the petals. In Butomaceae, the perianth is not differentiated and the development of the inner tepals is not delayed; the larger inner tepals (petals) only permit the initiation of stamens in antesepalous pairs. Alismataceae has delayed petals and the stamens are shifted close to the petals, leading to an association of stamen pairs with petals in so-called stamen–petal complexes. In the studied Hydrocharitaceae species, which have the monocot floral Bauplan, paired stamens are replaced by larger single stamens and the petals are not delayed. These results indicate that the origin of the floral Bauplan, at least in petaloid Alismatales, is closely linked to the position of stamen pairs and the rate of petal development. Although the petaloid Alismatales are not immediately at the base of monocot divergence, the floral evolution inferred from the results should be a key to elucidate the origin of the floral Bauplan of monocots.     

Evolution of the monocot gynoecium: evidence from comparative morphology and development in Tofieldia, Japonolirion, Petrosavia and Narthecium

We present new comparative morphological and developmental data on gynoecia of three genera of early-divergent monocots: Tofieldia (Tofieldiaceae, Alismatales), Petrosavia and Japonolirion (Petrosaviaceae, Petrosaviales) and one lilioid monocot: Narthecium (Nartheciaceae, Dioscoreales). Our data show significant differences between the genera examined, and are congruent with the splitting of former Nartheciaceae sensu Tamura (1998) into families Tofieldiaceae, Petrosaviaceae NB-cosistent with later and Nartheciacae (APG II 2003). Our investigation confirms the presence of at least partial carpel fusion in all taxa examined. Previous data indicating apocarpy in Japonolirion, some Petrosavia and Tofieldia could be due to late postgenital carpel fusion in these plants. Syncarpy also characterises other early-divergent monocot lineages such as Acoraceae and Araceae. It is most parsimonious to regard syncarpy as a primitive condition for monocots, but an alternative scenario suggests that apocarpy is plesiomorphic among monocots, involving multiple origins of syncarpy. The latter hypothesis is supported by significant differences between gynoecia of early-divergent monocots, including different modes of carpel fusion.     

单子叶植物高级分类阶元系统演化: matK、rbcL和18S rDNA序列的证据

基于两个叶绿体基因（matK和rbcL）和一个核糖体基因（18S rDNA）的序列分析,对代表了基部被子植物和单子叶植物主要谱系分支的86科126属151种被子植物（单子叶植物58科86属101种）进行了系统演化关系分析。研究结果表明由胡椒目Piperales、樟目Laurales、木兰目Magnoliales和林仙目Canellales构成的真木兰类复合群是单子叶植物的姐妹群。单子叶植物的单系性在3个序列联合分析中得到98％的强烈自展支持。联合分析鉴定出9个单子叶植物主要谱系（广义泽泻目Alismatales、薯蓣目Dioscorcales、露兜树目Pandanales、天门冬目Asparagalcs、百合目Liliales、棕榈目Arecales、禾本目Poales、姜目Zingiberales、鸭跖草目Commelinales）和6个其他被子植物主要谱系（睡莲目Nymphaeales、真双子叶植物、木兰目、樟目、胡椒目、林仙目）。在单子叶植物内,菖蒲目Acorales（菖蒲属Acorus）是单子叶植物最早分化的一个谱系,广义泽泻目（包括天南星科Araceae和岩菖蒲科Toficldiaccae）紧随其后分化出来,二者依次和其余单子叶植物类群构成姐妹群关系。无叶莲科Petrosaviaceac紧随广义的泽泻目之后分化出来,无叶莲科和剩余的单子叶植物类群形成姐妹群关系,并得到了较高的支持率。继无叶莲科之后分化的类群形成两个大的分支：一支是由露兜树目和薯蓣目构成,二者形成姐妹群关系：另一支是由天门冬目、百合目和鸭跖草类复合群组成,三者之间的关系在单个序列分析和联合分析中不稳定,需要进一步扩大取样范围来确定。在鸭跖草类复合群分支内,鸭跖草目和姜目的姐妹群关系在3个序列联合分析和2个序列联合分析的严格一致树中均得到强烈的自展支持,获得的支持率均是100％。但是,对于棕榈目和禾本目在鸭跖草类中的系统位置以及它们和鸭跖草目-姜目之间的关系,有待进一步解决。值得注意的是,无叶莲科与其他单子叶植物类群（除菖蒲目和泽泻目外）的系统关系在本文中获得较高的自展支持率,薯蓣目和天门冬目的单系性在序列联合分析中都得到了较好的自展支持,而这些在以往的研究中通常支持率较低。鉴于菖蒲科和无叶莲科独特的系统演化位置,本文支持将其分别独立成菖蒲目和无叶莲目Petrosavialcs的分类学界定。     

Gynoecium diversity and systematics of the basal eudicots

Gynoecium and ovule structure was compared in representatives of the basal eudicots, including Ranunculales (Berberidaceae, Circaeasteraceae, Eupteleaceae, Lardizabalaceae, Menispermaceae, Papaveraceae, Ranunculaceae), Proteales (Nelumbonaceae, Platanaceae, Proteaceae), some families of the former ‘lower’ hamamelids that have been moved to Saxifragales (Altingiaceae, Cercidiphyllaceae, Daphniphyllaceae, Hamamelidaceae), and some families of uncertain position (Gunneraceae, Myrothamnaceae, Buxaceae, Sabiaceae, Trochodendraceae). In all representatives studied, the carpels (or syncarpous gynoecia) are closed at anthesis. This closure is attained in different ways: (1) by secretion without postgenital fusion (Berberidaceae, Papaveraceae, Nelumbonaceae, probably Circaeaster); (2) by a combination of postgenital fusion and secretion; (2a) with a complete secretory canal and partly postgenitally fused periphery (Lardizabalaceae, Menispermaceae, some Ranunculaceae, Sabiaceae); (2b) with an incomplete secretory canal and completely fused periphery (Tro-chodendron); (3) by complete postgenital fusion without a secretory canal (most Ranunculaceae, Eupteleaceae, Platanaceae, Proteaceae, all families of Saxifragales and incertae sedis studied here). Stigmas are double-crested and decurrent in most of the non-ranunculalian taxa; unicellular-papillate in most taxa, but with multicellular protuberances in Daphniphyllaceae and Hamamelidaceae. Carpels predominantly have three vascular bundles, but five in Proteales (without Nelumbonaceae), Myrothamnaceae and Trochodendraceae. The latter two also share ‘oil’ cells in the carpels. Stomata on the outer carpel surface are present in the majority of Ranunculales and Proteales, but tend to be lacking in the saxifragalian families. In basal eudicots, especially in the non-ranunculalian families there is a trend to form more than one ovule per carpel but to develop only one seed, likewise there is a trend to have immature ovules at anthesis. Ovule number per carpel is predominantly one or two. Proteales (without Nelumbonales) mainly have orthotropous ovules, the other groups have anatropous (or hemitropous or campylotropous) ovules. The outer integument is annular in the groups with orthotropous or hemitropous ovules, and also in a number of saxifragalian families with anatropous ovules. In Proteales the integuments are predominantly lobed but there is no distinct pattern in this feature among the other groups. Among Ranunculales two pairs of families (Lardizabalaceae/Menispermaceae and Bcrberidaceae/Papaveraceae) due to similarities in gynoecium structure can be recognized, which are not apparent in molecular analyses. The close relationship of Platanaceae and Proteaceae is supported by gynoecium structure but gynoecial features do not support their affinity to Nelumbonaceae. The alliance of Daphniphyllaceae with Hamamelidaceae s.l. is also supported.     

Leaf Architecture of Some Monocotyledons with Reticulate Venation

Twelve species belonging to seven monocotyledonous families:Hydrocharitaceae, Taccaceae, Dioscoreaceae, Smilacaceae, Araceae,Alismataceae and Aponogetonaceae show reticulate venation typicalof dicotyledons. A study of the leaves of these species showsthat venation patterns are usually curvipalmate-convergate,occasionally rectipalmate or collimate, and rarely pinnate lyratetype. Number, size and shape of areoles, number of primaries,number of secondaries along one side of the primaries, anglebetween 1 and 2° veins and number of vein endings per areoleare given for each species. Intesecondary veins, isolated tracheids,loops, extension cells, raphide and raphide idioblasts and terminaltracheids were observed. Marginal ultimate venation is mostlyarcuate. Major and minor veins are jacketed by parenchymatousbundle sheath cells. The lamina of Tacca leontopetaloides, Colocasiaesculenta and Scindapsus aureus show a single midrib-like centralregion similar to that of dicotyledonous leaves, and it is multistrandedin Aponogeton natans, Limnophyton obtusifolium and Ottelia alismoides.The degree of vein order is most commonly up to fourth or fifthand rarely up to sixth in Dioscorea hispida. Monocotyledons, leaf architecture, vein endings, venation, areoles     

Gynoecium diversity and systematics of the Laurales

Carpel and ovule structure was comparatively studied in representatives of all eight families of the Laurales: Amborellaceae, Calycanthaceae, Chloranthaceae, Gomortegaceae, Hernandiaceae, Lauraceae, Monimiaceae, and Trimeniaceae. In all representatives the carpels are closed at anthesis. As in Magnoliales/winteroids, closure takes place in three different modes: (1) by postgenital fusion of the stylar (and ovarial) ventral slit (Calycanthaceae, Gomortegaceae, Lauraceae, Hernandiaceae); (2) by occlusion of the inner space by secretion (Amborellaceae, Chloranthaceae, Trimeniaceae, Mollinedioideae of Monimiaceae), all having extremely ascidiate carpels; (3) by a combination of (1) and (2), whereby the ventral slit in the style is postgenitally fused but a central canal remains open, which is filled by secretion (Monimiaceae except Mollinedioideae). The carpels have a single ovule in ventral median placentation; only Calycanthaceae have two lateral ovules, although the upper ovule degenerates. In contrast to Magnoliales/winteroids, several representatives have orthotropous or almost orthotropous ovules (Amborellaceae, Chloranthaceae, Gomortegaceae). Mature ovules vary in length between 425 μm (some Monimiaceae) and 1500 urn (some Calycanthaceae, Trimeniaceae). Although all ovules are crassinucellar, nucellus breadth varies between 60 μm (Chimonanthus, Calycanthaceae) and 500 μm (Hemandia, Hernandiaceae). In almost all representatives the single ovule (two in Calycanthaceae) tightly fills out the ovarial cavity. The micropyle is mostly formed by the inner integument. In a few cases there is no micropyle and the nucellar apex makes direct contact with the inner ovary surface or the funicle (Lauraceae p.p., Calycanthaceae p.p., Hernandiaceae p.p., Monimiaceae p.p.). The ovule is pachychalazal (or perichalazal) in Lauraceae, some Hernandiaceae, and Gomortegaceae. Both integuments are variously lobed or unlobed. The outer integument is semiannular or annular, and this may vary within a family (Calycanthaceae, Hernandiaceae, Monimiaceae); it is also exceedingly diverse in thickness (2–23 cell layers). Gynoecial traits support the association of Chloranthaceae, Trimeniaceae, and Amborellaceae, and also separately Gomortegaceae, Hernandiaceae, and Lauraceae. In addition, affinities of the first group with Schisandraceae, Illiciaceae and Austrobaileyaceae may also be supported.     

Chimiotaxinomie flavonique des fluviales

The flavonoid patterns of twenty-three species of Fluviales (= Helobieae) were determined. Flavonols and pro-anthocyanidins are uncommon and trihydroxy derivatives are absent. In contrast, flavones (luteolin and chrysoeriol derivatives) are common, often as C-glycosides (Alismataceae, Butomaceae, Potamogetonaceae). From a taxonomic point of view the results suggest that the Fluviales can be divided into two groups: Potamogetonaceae. Zosteraceae, Ruppiaceae, Zanichelliaceae and Juncaginaceae forming the first, and Hydrocharitaceae, Butomaceae. Alismataceae and Aponogetonaceae the second. This arrangement agrees for the most part with the views of Emberger and Takhtajan.

Résumé

Le contenu flavonique de 23 Fluviales (= Hélobiées) a été analysé. Flavonols et leuco-anthocyanes sont rares, les dérivés phényl-trihydroxylés absents. Les flavones, par contre, sont fréquentes (lutéoline, chrysoériol). notamment sous forme de C-glycosides (Alismatacées, Butomacées, Potamogétonacées). D'un point de vue taxinomique, les résultats permettent de regrouper, d'une part Potamogétonacées, Zostéracées, Ruppiacées. Zanichelliacées et Juncaginacées; d'autre part Hydrocharitacées, Butomacées, Alismatacées et Aponogétonacées. Cette proposition s'accorde dans ses grandes lignes avec les rues des botanistes Emberger et Takhtajan.     

最大似然法和贝叶斯推论与似然比检验探讨泽泻目系统发育关系

应用最大似然法(ML)、贝叶斯推论(BI)、邻接法(NJ)和似然比检验(hLRTs)进行泽泻目分子系统学研究。所用的rbcL基因序列代表了泽泻目14科46属以及作为外类群的6相关属。研究结果表明,*等级制似然比检验表明泽泻目rbcL序列最适合的DNA进化模型为GTR+I+G,最大似然法、贝叶斯法和邻接法构建的系统发育树拓扑结构相似,没有显著的差异,但贝叶斯树支持率较高;泽泻目为一单系类群,由两个主要谱系分支构成,深层分布格局由5个主要分支构成。基于分子系统发育树,文中对泽泻目科间、水鳖科+茨藻科、泽泻科+花蔺科+黄花蔺科、和"Cymodoeaceae complex"的系统发育关系进行了讨论。研究结果还表明,泽泻目系统发育关系可能还需要更多的证据进一步的澄清。     

Phylogenetic Studies in the Monocot Subclass Alismatidae: Evidence for a Reappraisal of the Aquatic Order Najadales

Within the angiosperm subclass Alismatidae (= superorder Alismatiflorae), contemporary taxonomists have often assigned the families Hydrocharitaceae and Najadaceae to different orders. The Najadaceae are presumably allied to a variety of aquatic families in the order Najadales, whereas the Hydrocharitaceae have been segregated as the order Hydrocharitales or placed within the order Alismatales. Analyses of DNA sequence data from the chloroplast gene rbcL, however, indicate that Najadaceae have a much closer phylogenetic relationship to Hydrocharitaceae than to families of the "Najadales" (Cymodoceaceae, Potamogetonaceae, Ruppiaceae, Scheuchzeriaceae, Zannichelliaceae, Zosteraceae). This association supports previous studies based upon examination of floral structure and seed coat anatomy. The rbcL sequence data also indicate that the Zosteraceae and Potamogetonaceae are closely related families. The rbcL sequence of Zostera is actually more similar to that of Potamogeton richardsonii than is the sequence of the latter to a congener, Potamogeton amplifolius. The marine, dioecious, hydrophilous genus Zostera has acquired a number of distinctive adaptations, but probably diverged relatively rapidly from freshwater Potamogetonaceae. Molecular data place Ruppiaceae as a sister group to the marine Cymodoceaceae and do not support the commonly accepted merger of Ruppiaceae and Potamogetonaceae.     

Morphology of Maundia supports its isolated phylogenetic position in the early‐divergent monocot order Alismatales

According to recent molecular phylogenetic data, the rare Australian endemic Maundia triglochinoides does not form a clade with taxa traditionally classified as members of Juncaginaceae. Therefore, views on the morphological evolution and taxonomy of Alismatales require re‐assessment. As the morphology of Maundia is poorly known and some key features have been controversially described in the literature, the flowers, fruits, inflorescence axes and peduncles were studied using light and scanning electron microscopy. Inflorescences are bractless spikes with flowers arranged in trimerous whorls. Except in the inflorescence tip (where the flower groundplan is variable), flowers possess two tepals in transversal‐abaxial positions, six stamens in two trimerous whorls and four carpels in median and transversal positions. Fruits are indehiscent. The shared possession of orthotropous ovules supports the molecular phylogenetic placement of Maundia as sister to a large clade including Potamogetonaceae and related families. Maundia and Aponogeton spp. share the same highly unusual floral groundplan, a homoplastic similarity that can be explained by spatial constraints in developing inflorescences. The nucellar coenocyte of Maundia appears to be unique among monocots. As Maundia exhibits a mosaic of features characteristic of other families of tepaloid core Alismatales, its segregation as a separate family is plausible. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 173 , 12–45.     

Gynoecium diversity and systematics of the paleoherbs

Gynoecium and ovule structure was compared in representatives of all families of the paleoherbs, including Nymphaeales (Cabombaceae, Nymphaeaceae), Piperales (Saururaceae, Piperaceae), Aristolochiales (Lactoridaceae, Aristolochiaceae), Rafflesiales (Hydnoraceae, Rafflesiaceae) and, in addition, Ceratophyllaceae and Nelumbonaceae, both of which were earlier included in Nymphaeales, but then segregated and with an unestablished position. In all representatives studied, the carpels are closed at anthesis. Carpel closure is attained in three different ways: (1) postgenital fusion of inner surfaces (Piperales, Aristolochiales); (2) occlusion by secretion or mutual appression of inner surfaces without postgenital fusion (Cabombaceae, Ceratophyllaceae, Nelumbonaceae (?) or (3) strong secretion combined with postgenital fusion at the periphery of the carpel (Nymphaeaceae). In Cytinus (Rafflesiaceae), after an earlier developmental stage with apparent postgenital fusion there is strong internal secretion (within the cell walls). Stigma shape tends to be double-crested in the basal taxa of each order: Cabombaceae (Brasenia), Saururaceae, and Lactoridaceae. In some Aristolochiaceae and Cytinus (Rafflesiaceae) they have two lobes in the transverse symmetry plane (i. e. at right angles to the median plane) or, if the carpels are united, the stigmatic lobes are commissural, accordingly. Stigmas are unicellular papillate and secretory in most taxa, but the papillae are uniseriate-pluricellular in some (not basal) Nymphaeaceae, Asaroideae (Aristolochiaceae) and Cytinus (Rafflesiaceae). Ceratophyllaceae have smooth stigmas. Intrusive oil cells in the carpel epidermis were found in Piperales and Aristolochiaceae. Mature ovules vary in length between 0. 2 mm and 2. 5 mm. Mature nucelli vary in breadth between 0. 03 mm and 1. 6 mm. These differences are larger than in the other major magnoliid groups. The outer integument is fully annular (not semiannular) in all taxa with orthotropous ovules (all Piperales and Barclaya of Nymphaeaceae) and also in some with anatropous ovules (some Nymphaeaceae, some Aristolochiaceae). The integuments are variously lobed or unlobed; both integuments tend to exhibit the same behaviour within a family, either both lobed or both unlobed. The results strongly support three pairs of families in sister group relationships, as suggested by studies based on other characters: Cabombaceae-Nymphaeaceae, Saururaceae-Piperaceae, and Lactoridaceae-Aristolochiaceae, and Hydnoraceae-Rafflesiaceae to some extent. Piperales and Aristolochiales are closer to each other than either is to Nymphaeales. Nelumbonaceae is isolated, as is Ceratophyllaceae, but the status of the latter is more difficult to interpret owing to apparent reduction in morphological, anatomical and histological traits.     

水鳖科9属15种植物花粉形态的研究

应用光学显微镜、扫描电镜和透射电镜对水鳖科Hydrocharitaceae 9属15种植物的花粉形态进行 了观察。水鳖科植物花粉为圆球形至近椭球形,无萌发孔或偶为单沟萌发孔,外壁纹饰通常为小刺状纹 饰,刺密集或稀疏,花粉表面具瘤状、疣状、颗粒状、皱波状突起或光滑。外壁由覆盖层、柱状层和基层组 成。覆盖层厚或较薄,柱状层小柱发育不明显,基层薄。水鳖科植物在花粉大小、纹饰类型、刺的长短、 密度、形态、萌发孔的有无以及花粉壁的结构等方面表现出了较为明显的差异,这些特征对探讨类群间 关系具有较重要意义。由于黑藻属Hydrilla和Stratiotes属花粉较为特殊,支持将它们各自作为一个独立 的族处理。水鳖科植物花粉外壁纹饰和结构特点表明该科与水雍科Aponogetonaceae、泽泻科Alismataceae 和花蔺科Butomaceae等近缘,而该科植物花粉大多无萌发孔等则反应了该科与茨藻目Najadales植物有密切联系。     

Patterns of angiospermy development before carpel sealing across living angiosperms: diversity,and morphological and systematic aspects

Almost all angiosperms are angiospermous, i.e. the ovules are enclosed in carpels at anthesis and during seed development, but angiospermy develops in different ways across angiosperms. The most common means of carpel closure is by a longitudinal ventral slit in carpels that are partly or completely free. In such carpels, the closure process commonly begins at midlength of the prospective longitudinal slit and then proceeds downward and upward. Closure by a transverse slit is rarer, but it is prominent in groups of the ANITA grade and in a few early branching monocots (some Alismatales) and some early branching eudicots (a few Ranunculaceae and Nelumbonaceae), in these eudicots combined with a more or less developed longitudinal slit. In all these cases the carpels have a single ovule in ventral median position. In ANITA lines with pluriovulate carpels, there is only a short longitudinal slit in the uniformly ascidiate carpels. In carpels with a unifacial style the closure area is narrow; this pattern is rare and scattered mainly in some wind‐pollinated monocots and eudicots. In most angiosperms the carpels become closed before the ovules are visible from the outside of the still incompletely closed carpels (early carpel closure). This is notably the case in the ANITA grade and magnoliids. Delayed carpel closure, with the ovules visible before the carpels are closed, is much rarer and is concentrated in a few monocots (mainly some Alismatales and some Poales) and a few eudicots (mainly a few Ranunculales and many Caryophyllales, and scattered in some other eudicots). A kind of delayed carpel closure (with the placenta visible before closure but mostly not the ovules) also occurs in syncarpous gynoecia with a free central placenta. Most gynoecia with a free central placenta occur in the superasterids. In such gynoecia the individual carpel tips are not differentiated but the opening in young gynoecia has the shape of a circular diaphragm. In this case, when ovary septa and free carpel tips are missing, the number of carpels is sometimes unclear (Primulaceae, Lentibulariaceae, some Santalaceae). Extremely ascidiate carpels are concentrated in the ANITA grade, a few magnoliids and some early branching monocots. Aspects of potential advantages of plicate vs. ascidiate carpels with regard to flexibility of pollen tube transmitting tract differentiation are discussed. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 178 , 556–591.     

湖北省泽泻科、水鳖科、眼子菜科及茨藻科植物花粉形态研究

本文利用光镜及扫描电镜对湖北省泽泻科、水鳖科、眼子菜科及茨藻科11属29种1变种1变型植物(另加采于湛江的软骨草)的花粉形态进行了研究,发现泽泻科植物花粉具多个圆形萌发孔,外壁表面为小刺状纹饰;茨藻科植物花粉具远极单槽,表面为绉波状纹饰;眼子菜科及本文研究的水鳖科植物花粉均无萌发孔,分别具网状和小刺状饰纹饰。1.茨藻科植物花粉最原始,泽泻科花粉较进化,眼子菜科花粉较水鳖科花粉进化;2.泽泻属与泽苔草属花粉较慈姑属花粉原始;3.鞘叶眼子菜亚屈花粉较眼子菜亚属的花粉处于更高演化阶段;4.多孔茨藻花粉在该科中最原始。本文工作尚对易变形水生植物花粉形态研究方法进行了尝试。     

Flower-like terminal structures in racemose inflorescences: a tool in morphogenetic and evolutionary research

Terminal flower-like structures (TFLS) occur in many angiosperms that possess indeterminate inflorescences such as spikes, racemes, or spadices. We describe and review TFLS in early-divergent angiosperms, especially the magnoliid order Piperales and the monocot order Alismatales, in which floral interpretation is controversial. Essentially similar TFLS occur in a wide range of taxa. Among magnoliids, they occur in some Piperales (Saururaceae and a few Piperaceae), but are absent from Chloranthaceae. Among monocots, they occur in some early-divergent families such as Acoraceae, Aponogetonaceae, Juncaginaceae, Potamogetonaceae, and Ruppiaceae. Similar TFLS with obscure organ identity are recorded in mutants of Arabidopsis. TFLS can often be interpreted as pseudanthia (close aggregations of reduced flowers), but in some cases the entire terminal pseudanthium is very similar to a true flower. In some cases, elaborated TFLS could therefore have given rise to what are normally termed 'true' (i.e. euanthial) flowers. Data presented here on terminal pseudanthia in Potamogeton and Ruppia support a pseudanthial evolutionary origin of reproductive units in the alismatid families Zannichelliaceae and Cymodoceaceae. Furthermore, in some alismatid species, either the entire inflorescence apex or an individual primordium at or near the inflorescence tip can be transformed into a filamentous or tubular (or intermediate) structure. A tubular structure enclosing stamens and carpels is described in Piper. This indicates that pseudanthium formation can provoke morphological novelties, perhaps due to new patterns of overlap between expression zones of regulatory genes and/or new spatial constraints.     

Mycorrhizae in Monocotyledonae of Northeast Brazil: subclasses Alismatidae, Arecidae and Zingiberidae

 We studied the mycorrhizal condition of three subclasses (Alismatidae, Arecidae, Zingiberidae) of Liliopsida (Monocotyledonae) occurring in different natural areas of the State of Pernambuco, Northeast Brazil. Twenty-two of 35 specimens (62.8%) were colonized by arbuscular mycorrhizal (AM) fungi. No association was found in specimens of five families (Alismataceae, Cannaceae, Cyclanthaceae, Hydrocharitaceae, Limnocharitaceae), but in two other families (Costaceae, Zingiberaceae) all specimens formed mycorrhizae. Four families showed variable mycotrophy (Araceae, Bromeliaceae, Heliconiaceae, Marantaceae). This is the first evaluation of the mycorrhizal condition of 24 Monocotyledonae species from this region, 15 of which were found to form AM. Accepted: 4 July 2000     

水雍科植物的花粉形态研究

应用光学显微镜、扫描电镜和透射电镜对世界水雍科6种植物的花粉形态进行了观察。水雍科植物花粉为舟形或船形,具远极单沟萌发孔类型,外壁纹饰通常为浅网状至网状,稀为小刺状纹饰,外壁外层由覆盖层、柱状层和基层组成,覆盖层厚。水雍科植物花粉外壁纹饰表现了从小刺状向网状的过渡。该科花粉为远极单沟,覆盖层厚,具小刺等特征反映了其与水鳖科和泽泻目花蔺科的密切联系,而该科花粉外壁纹饰多为网状则与茨藻目植物接近。这一结果支持将水雍科从茨藻目中分出作为一个独立的目处理的观点。此外,水雍科植物的花粉大小、纹饰类型、网眼大小与深浅等方面的差异对种级分类有一定意义。     

Cytogenetics of Alismatales s.s.: chromosomal evolution and C-banding

Ten species of Alismatales, five of Alismataceae, four of Limnocharitaceae and one of Hydrocharitaceae were studied with regard to chromosome number, chromosome morphology, and pattern of Giemsa C-bands. The genus Echinodorus had a diploid chromosome number of 22 for all species that were analyzed and a karyotypic formula of 2m + 20a. For the family Limnocharitaceae, Hydrocleys nymphoides had a diploid chromosome number of 16, Hydrocleys martii (4m + 2sm + 10a) had a diploid chromosome number of 16, Limnocharis flava had a diploid chromosome number of 20 and L. laforestii (4m + 16a) had a diploid chromosome number of 20. The only species of Hydrocharitaceae that was studied exhibited a karyotype that consisted of a diploid chromosome number of 28 and a karyotypic formula of 4m + 6sm + 4a. The distribution pattern of the C-banded karyotype in Echinodorus showed four blocks of constitutive heterochromatin in two smaller acrocentric pairs that corresponded to the heterochromatic NORs. In E. lanceolatus, 14 bands in the termini of the arms beyond the heterochromatic NORs of seven acrocentric pairs were also observed. Idiograms are presented and the karyotypic evolution patterns for the studied groups are discussed.     

Developmental morphology of the ovules of Amborella trichopoda (Amborellaceae) and Chloranthus serratus (Chloranthaceae)

The developmental morphology of the outer integument in the pendent orthotropous ovules of Amborella trichopoda (Amborellaceae) and Chloranthus serratus (Chloranthaceae) was studied. In both species the outer integument is semiannular at an early stage and becomes cup-shaped but dorsiventrally somewhat asymmetric at later stages. The outer integument, which is initiated first on the concave and lateral sides of the ovule, differs from that of the anatropous ovules of other basal families with the outer integument semiannular at an early stage or throughout development. The bilateral symmetry of the outer integument is shared by these orthotropous and anatropous ovules. The developmental pattern of the outer integument and ovule incurving characterize the ovule of the Amborellaceae and Chloranthaceae, which is not equivalent to typical orthotropous ovules of eudicots. A phylogenetic analysis of ovule characters in basal angiosperms suggests that anatropous ovules with cup-shaped outer integuments and orthotropous ovules were derived independently in several clades and that the ovules of Amborella and Chloranthus might also be derivative.