Gynoecium diversity and systematics of the Magnoliales and winteroids

Carpel and ovule structure was compared in representatives of all 11 families of the Magnoliales (Annonaceae, Canellaceae, Degeneriaceae, Eupomatiaccae, Himantandraceae, Magnoliaceae, Myristicaceae) and winteroids (Austrobaileyaceae, Illiciaceae, Sehisandraceae, Winteraceae). Special attention was paid to features that are constant at family level. Bisexual flowers are always protogynous. In all representatives studied the carpels are closed at anthesis. Caipel closure is attained in three different ways: (1) postgenital fusion of inner surfaces (Degeneriaceae, Eupomatiaccae. Winteraceae), or (2) occlusion by secretion (Austrobaileyaceae, Sehisandraceae), or (3) a combination of (1) and (2): in Annonaceae, Canellaceae, Myristicaceae there is a conspicuous secretory canal in the innermost part of the ventral slit; in Illiciaceae and Magnoliaceae there is a narrow canal in the innermost part of the ventral slit; and in Himantandraceae the ventral slit is postgenilally fused in the style but completely open in the ovary. In most families the carpels have a double stigmalic crest or they have two tips in the transversal symmetry plane (i.e. at right angles to the median plane). Stigmas are unicellular papillate in most families but the papillae are bi-to multicellular (uniseriate) in Degeneriaceae and Eupomatiaceae. An unusual cryptic exlracarpellary compitum was found in Himantandraceae and Sehisandraceae. Intrusive oil cells were found in the carpel epidermis of Illiciaceae and Sehisandraceae. Mature ovules vary in length between 0.15 and 1.1 mm. The outer integument is fully annular (not semiannular) in Degeneriaceae, Himantandraceae, Canellaceae, Myristicaceae, and Illiciaceae. A rudimentary aril occurs in Canellaceae, and originates at the same site as in arillate Annonaceae and Myristicaceae. The results most strongly support an Annonaceae-Myristicaceae-Canellaceae alliance, to some degree also an Eupomatiaccac-Degeneriaceae-Himantandraceae-Magnoliaceae alliance, and an Illiciaceae-Schisandraceae-Winteraccae-Austrobaileyaceae alliance.     

Alkaloid evolution and angiosperm systematics

The correlation of biosynthetic steps leading to the primary precursors of the shikimate pathway with the distribution of derived alkaloids on dahlgren's system of classification of angiosperm orders suggests that evolution paralleled gradual blocking of these steps. Phenylalanine-derived alkaloids, with the centre of radiation situated in the magnoliales, are of widespread occurrence in angiosperms, an indication of the antiquity of the character. Anthranilic acid-derived alkaloids, with the centre of radiotion in the rutales, are less widespread. Orders in which such alkaloids co-occur with the former biogenetic group are considered to be of more recent origin. Finally, mevalonate-derived iridoid alkaloids, with the centre of radiation in the gentianales, are even less widespread. Orders in which such alkaloids co-occur with the former biogenetic groups should thus be of still more recent origin. These concepts are summarized bg a phylogenetic tree, which illustrates the divergence of three major groups of angiosperm superorders.     

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.     

被子植物异型花柱及其进化意义

异型花柱(heterostyly)是被子植物中一种特殊的花多态现象和雌雄异位形式,包括二型花柱(distyly)和三型花柱(tristyly)2种类型.据报道,在被子植物的约31个科中有异型花柱植物.该类型植物的花部特征在避免自交、促进准确的异交传粉以及通过降低雌雄功能干扰以提高亲本适合度等方面具有重要的进化意义.该文从以下3个方面总结和分析了异型花柱及其进化意义:(1)异型花柱植物的类型和花部特征、附属多态性和种群结构:(2)异型花柱植物在被子植物中的分布、起源和演化:(3)异型花柱植物的进化适应意义.结合目前作者开展的有关工作,对异型花柱植物研究中存在的一些问题进行讨论和展望,希望能为国内工作者开展该领域的研究提供一些参考.     

被子植物成花诱导和性别决定机制的研究进展

开花植物具有多样性的生殖系统,其中单性花的形成是促进异交、避免自交衰退、保持遗传多样性的重要途径。单性花物种分布于被子植物不同进化分支上的事实表明,物种的雌雄异花性可能是通过不同的机制进化形成的。本文从花发育、性染色体、植物激素和环境因素四个方面,阐述了被子植物性别分化调控机制的研究进展。     

Schmeissneria: An angiosperm from the Early Jurassic

The origin of angiosperms has been a focus of intensive research for a long time. The so-called preCretaceous angiosperms, including Schmeissneria, are usually clouded with doubt. To expel the cloud around the enigmatic Schmeissneria, the syntype and new materials of Schmeissneria collected previously in Germany and recently in China are studied. These materials include female inflorescences and infructescences. The latter are old materials but were under-studied previously. Light microscopy and scanning electron microscope observations indicate that the fruits in these infructescences have in situ seeds enclosed, and that the ovaries are closed before pollination. Thus the plants meet two strict criteria for angiosperms: angiospermy plus angio-ovuly. Placing Schmeissneria in angiosperms will extend the record of angiosperms up to the Early Jurassic, more compatible with many molecular dating conclusions on the age of angiosperms, and demanding a reassessment of the current doctrines on the origin of angiosperms. Although the phylogenetic relationship of Schmeissneria to other angiosperms apparently is still an open question, this study adds to research concerning the origin of angiosperms.     

Systematics, biogeography and conservation of Lactoridaceae

Lactoridaceae are a monotypic family confined to the Juan Fernandez (= Robinson Crusoe) Islands, Chile, an archipelago four million years old. Interest in the lone species, Lactoris fernandeziana, has increased in recent years due to its suspected role in early angiosperm evolution, as well as its endangered conservation status. Reports of fossil pollen of Lactoris (as Lactoripollenites) from deep sea sediments of Cretaceous age off the western coast of South Africa provide evidence for southern hemisphere occurrence of the family 70–90 million years ago. This age, plus trimerous symmetry and simple morphology of the flower with three tepals, six stamens and three nearly free carpels with laminar placentation, involve the family with hypotheses regarding evolution of early angiosperms, especially paleoherb and monocot divergences. Based on cladistic analyses with morphological and nucleotide data, recommended taxonomic placement of Lactoris is as a monotypic order, Lactoridales, allied most closely to Aristolochiales, and also near Piperales. Approximately 1000 individuals of Lactoris are believed to exist, and genetic variation within and among populations as measured by isozymes and RAPDs is low. This, in part, could be due to the self-compatibility and geitonogamous breeding system of this wind-pollinated species. More efforts at ex situ conservation should be attempted so that this important angiosperm family is maintained for future evolutionary studies.     

The distribution and systematic relevance of the androecial character oligomery

Localization of the stamens can be approached by a preliminary distinction between two characters, oligomery and polymery, occurring in two different groups of taxa, respectively the oligomerous complex and the polymerous complex. Oligomery is described by four character states standing in a close semophyletic relationship: diplostemony, obdiplostemony, haplostemony and obhaplostemony. Each character state is analysed for its distribution and systematic value. Diplostemony is the synapomorphic character state for the oligomerous line and has arisen once from a polymerous ancestor or in parallel in different lines. Obdiplostemony arises ontogenetically in three different ways. Loss of one whorl leads either to obhaplostemony, or haplostemony; both character states are believed to represent evolutionary steps of no-return. Secondary increases and reductions of the stamens within a whorl are seen as expressions of the intrinsic variability of the character states and should not be homologized with them. Stamen numbers can be increased by the building-up of complex primordia or by secondary receptacular growth. Reductions of stamens affect one or two whorls of stamens and are caused by lack of space, interactions with the gynoecium and zygomorphy. The distribution of the different character states of oligomery is presented on Dahlgrenograms and the androecia of a number of families and their relationships are discussed. The interactions between oligomery and polymery are analysed as guidelines for a global phylogeny of the Magnoliatae.     

Defining the limits of flowers: the challenge of distinguishing between the evolutionary products of simple versus compound strobili

Recent phylogenetic reconstructions suggest that axially condensed flower-like structures evolved iteratively in seed plants from either simple or compound strobili. The simple-strobilus model of flower evolution, widely applied to the angiosperm flower, interprets the inflorescence as a compound strobilus. The conifer cone and the gnetalean ‘flower’ are commonly interpreted as having evolved from a compound strobilus by extreme condensation and (at least in the case of male conifer cones) elimination of some structures present in the presumed ancestral compound strobilus. These two hypotheses have profoundly different implications for reconstructing the evolution of developmental genetic mechanisms in seed plants. If different flower-like structures evolved independently, there should intuitively be little commonality of patterning genes. However, reproductive units of some early-divergent angiosperms, including the extant genus Trithuria (Hydatellaceae) and the extinct genus Archaefructus (Archaefructaceae), apparently combine features considered typical of flowers and inflorescences. We re-evaluate several disparate strands of comparative data to explore whether flower-like structures could have arisen by co-option of flower-expressed patterning genes into independently evolved condensed inflorescences, or vice versa. We discuss the evolution of the inflorescence in both gymnosperms and angiosperms, emphasising the roles of heterotopy in dictating gender expression and heterochrony in permitting internodal compression.     

中国白垩纪被子植物花粉的宏演化

根据中国白垩纪被子植物花粉产出记录与形态构造分析以及与世界其它地区产出顺序比较,假设中国白垩纪被子植物花粉的宏演化序列,共划分为１０个发育阶段,归于７个形态演化期：１）欧特里夫期至早巴列姆期的无口器类演化期（含：１：１网纹无口器粉发育阶段）;２）晚巴列姆至晚阿普梯期的单沟类演化期（含：２：１。棒纹粉发育阶段;２．２,星粉－棒纹粉发育阶段）;３）早,中阿尔必期的三沟类演化期（含：３．１,三沟粉类－星     

The flora of the early Miocene Brandon Lignite, Vermont, USA. VIII. Caldesia (Alismataceae)

Caldesia, a genus of aquatic monocotyledons, is represented by four living species, which are widely distributed in the temperate and tropical Old World. The genus has an extensive Oligocene through Pleistocene fossil record in Eurasia. We survey the morphology of the extant and fossil fruits of the Alismataceae, and provide a detailed review of the morphology and anatomy of living and fossil Caldesia fruits. The latter exhibit substantial similarity, making the recognition of separate species on the basis of fruit morphology difficult. We erect the new species Caldesia brandoniana from the Early Miocene Brandon Lignite of Vermont primarily on the basis of its geographic isolation; careful revision of all fossil fruiting material of Caldesia might require placement of the Brandon specimens in a more inclusive form species. Together with leaves of Caldesia from the Miocene Clarkia flora of Idaho, this occurrence indicates that Caldesia was in the New World as recently as the Early Miocene.     

The evolutionary-developmental analysis of plant microRNAs

MicroRNAs (miRNAs) control many important aspects of plant development, suggesting these molecules may also have played key roles in the evolution of developmental processes in plants. However, evolutionary-developmental (evo-devo) studies of miRNAs have been held back by technical difficulties in gene identification. To help solve this problem, we have developed a two-step procedure for the efficient identification of miRNA genes in any plant species. As a test case, we have studied the evolution of the MIR164 family in the angiosperms. We have identified novel MIR164 genes in three species occupying key phylogenetic positions and used these, together with published sequence data, to partially reconstruct the evolution of the MIR164 family since the last common ancestor of the extant flowering plants. We use our evolutionary reconstruction to discuss potential roles for MIR164 genes in the evolution of leaf shape and carpel closure in the angiosperms. The techniques we describe may be applied to any miRNA family and should thus enable plant evo-devo to begin to investigate the contributions miRNAs have made to the evolution of plant development.