被子植物的起源-以喜花虻类化石为据

喜花昆虫在被子植物的起源和早期演化上起着决定性的作用。虻类化石中的许多类群都有访花习性,它们为研究被子植物的起源提供了独特材料。虽然最老的被子植物化石还没有发现,但是喜花虻类的爆发式出现,表示了被子植物出现的时间和地点。本文主要以欧亚大陆东部,特别是中国辽西的侏罗杨虻类化石为材料,在功能形态分析和与现代类群作对比的基础上,证证实了虻类是显花植物最原始的传粉类群之一。中国东北、哈萨克斯坦和西伯利来晚     

睡莲科系统位置评述

形态学研究显示睡莲科Nymphaeaceae具有许多原始性状。睡莲科又被称为“古草本”。最新的分子系统发育研究显示,睡莲科是现存被子植物系统树根部附近最早分异谱系的演化支之一,对研究被子植物(有花植物)的起源与早期进化具有重要价值,但有关睡莲科的范围和系统位置存在争议。被子植物的起源与辐射一直是植物学家关注的热点。本文对该科系统位置的研究历史与现状进行了评述。     

莲科系统位置评述

莲科含1属1种2亚种,以具有最古老的有活力的种子而著称。形态学研究显示,莲不仅具有双子叶植物特征,而且又具有单子叶植物的某些性状。因此,对研究被子植物(有花植物)的起源与演化以及单子叶植物的起源具有重要价值。被子植物(有花植物)的起源与辐射一直是植物学家关注的热点,有关莲科的系统位置存在争议。该文对该科系统位置的研究历史与现状进行评述。     

Convergent evolution and adaptive radiation of beetle-pollinated angiosperms

A literature review of 34 families of flowering plants containing at least one species pollinated primarily by beetles is presented. While the majority of species are represented by magnoliids and basal monocotyledons specialized, beetle-pollinated systems have evolved independently in 14 families of eudicotyldons and six families of petaloid monocots. Four, overlapping modes of floral presentation in plants pollinated exclusively by beetles (Bilabiate, Brush, Chamber Blossom and Painted Bowl) are described. Chamber Blossoms and Painted Bowls are the two most common modes. Chamber Blossoms, found in magnoliids, primitive monocotyledons and in some families of woody eudicots, exploit the greatest diversity of beetle pollinators. Painted Bowls are restricted to petaloid monocots and a few families of eudicots dependent primarily on hairy species of Scarabaeidae as pollen vectors. In contrast, generalist flowers pollinated by a combination of beetles and other animals are recorded in 22 families. Generalist systems are more likely to secrete nectar and exploit four beetle families absent in specialist flowers. Centers of diversity for species with specialized, beetle-pollinated systems are distributed through the wet tropics (centers for Brush and Chamber Blossoms) to warm temperate-Mediterranean zones (centers for Painted Bowls and a few Bilabiate flowers). It is unlikely that beetles were the first pollinators of angiosperms but specialized, beetlepollinated flowers must have evolved by the midlate Cretaceous to join pre-existing guilds of beetlepollinated gymnosperms. The floras of Australia and western North America suggest that mutualistic interactions between beetles and flowers has been a continuous and labile trend in angiosperms with novel interactions evolving through the Tertiary.     

Triuridaceae fossil flowers from the Upper Cretaceous of New Jersey

We report here on a series of fossil flowers exhibiting a mosaic of characters present in the extant monocot family Triuridaceae. Phylogenetic analyses of morphological data from a broad sample of extant monocots confirm the affinities of the fossils with modern Triuridaceae. The fossil flowers were collected from outcrops of the Raritan Formation (Upper Cretaceous, ～90 million years before present), New Jersey, USA. These are the oldest known unequivocal monocot flowers. Because other reports of "earliest" monocots are all based on equivocal character suites and/or ambiguously preserved fossil material, the Triuridaceae fossils reported here should also be considered as the oldest unequivocal fossil monocots. Flowers are minute and unisexual (only male flowers are known); the perianth is composed of six tepals, lacking stomata. The unicyclic androecium is of three stamens with dithecal, monosporangiate, extrorse anthers that open by longitudinal slits. The endothecium has U-shaped type thickenings. Pollen grains are monosulcate. The triurid fossil flowers can be separated into three distinctive species. On the basis of phylogenetic analyses of morphological characters, the fossil taxa nest within the completely saprophytic achlorophyllous Triuridaceae supporting the interpretation that the extinct plants were also achlorophyllous and saprophytic. If so, this represents the earliest known fossil occurrence of the saprophytic/mycotrophic habit in angiosperms.     

A perfect flower from the Jurassic of China

Flower, enclosed ovule and tetrasporangiate anther are three major characters distinguishing angiosperms from other seed plants. Morphologically, typical flowers are characterised by an organisation with gynoecium and androecium surrounded by corolla and calyx. Theoretically, flowers are derived from their counterparts in ancient ancestral gymnosperms. However, as for when, how and from which groups, there is no consensus among botanists yet. Although angiosperm-like pollen and angiosperms have been claimed in the Triassic and Jurassic, typical flowers with the aforesaid three key characters are still missing in the pre-Cretaceous age, making many interpretations of flower evolution tentative. Thus searching for flower in the pre-Cretaceous has been a tantalising task for palaeobotanists for a long time. Here, we report a typical flower, Euanthus paniigen. et sp. nov., from the Middle–Late Jurassic of Liaoning, China. Euanthus has sepals, petals, androecium with tetrasporangiate dithecate anthers and gynoecium with enclosed ovules, organised just like in perfect flowers of extant angiosperms. The discovery of Euanthus implies that typical angiosperm flowers have already been in place in the Jurassic, and provides a new insight unavailable otherwise for the evolution of flowers.     

Introduction and Notes to R. Dahlgren's System of Classification of the Angiosperms

The present paper aims at introducting Dahlgren’s system of classification of the angiosperms. Phenetic and phylogenetic classifications are discussed. The basic principles and methods used by Dahlgren are explained. Dahlgren’s opinions on some important problems, such as the origin of angiosperms, the flowers of primitive angiosperms, the relation between the dicotyledons and monocotyledons, the origin of the monocotyledons, the treatment of the “Amentiferae” and of the orders of the “Sympetalae”, are all expressed. A brief comparison between Dahlgren’s system and three other current systems, viz. those of Takhtajan, Cronquist and Thorne is also given.     

被子植物雌全同株性系统:系统演化、性表达与进化意义

雌全同株是指雌花和两性花共同发生在同一植株上的性表达形式。作为被子植物从雌雄同花(两性花)向雌雄同株异花进化的一个重要阶段,雌全同株性系统在减少昆虫对雌性的取食和伤害、提高异交率以减少近交衰退、减少雌/雄功能干扰、提高雌/雄性功能间资源分配的灵活性,以及吸引传粉者等方面具有重要的进化适应意义。根据APG III分类系统,雌全同株性系统在被子植物木兰分支(magnoliids)的短蕊花科、单子叶植物分支(monocots)的天南星科和禾本科,以及核心真双子叶植物分支(core eudicots)中的菊科、苋科、唇形科和石竹科等23科中均有报道,且以菊科植物中最多。雌全同株植物不同类群的雌花和两性花在位置、形态、大小及开花时间等性表达特征上表现出多样化,且这些特征不仅受遗传因子的调控,还受可获得资源(如营养、光照、温度和水分等条件)的制约。该文针对我国对雌全同株性系统的研究还相对较少的现状,重点对具雌全同株性系统的类群在被子植物中的分布与系统演化、性表达与环境的关系等方面进行了分析与总结,并对有关其进化适应意义的5个假说进行了介绍和评价,对今后的研究方向进行了展望,以期为推动我国对被子植物雌全同株性系统的进化式样与机制研究提供理论资料。     

The evolution of embryogeny in seed plants and the developmental origin and early history of endosperm

For almost a century, the formation of endosperm from a second and distinctive fertilization event has been viewed as a unique feature of flowering plants. However, until recently, the evolutionary origin of this unique embryo-nourishing entity remained a mystery. Based upon comparative developmental analysis of reproduction among basal angiosperms and their closest extant relatives, the Gnetales (Ephedra, Gnetum, and Welwitschia), it is possible to construct an explicit hypothesis of the events that led to the evolutionary establishment of double fertilization and endosperm. The formulation of this historical record is derived entirely from and dependent upon the determination of reproductive features that are likely to have characterized the common ancestors of angiosperms and Gnetales. Current evidence is most congruent with the concept that a process of double fertilization first evolved in a common ancestor of the Gnetales and angiosperms. Initially, however, the second fertilization product was diploid and yielded a supernumerary embryo. Subsequent to the divergence of the angiosperm lineage from its closest relatives (which include the Gnetales), modification of the development of the supernumerary embryo (derived from the second fertilization event) led to the establishment of an embryo-nourishing endosperm. Comparative analysis of patterns of embryogeny within Gnetales and angiosperms establishes that embryo development in the ancestors of flowering plants (with a rudimentary process of double fertilization) was ab initio cellular, and not free nuclear, as had previously been assumed. Thus, it is likely that the earliest flowering plants displayed an ab initio cellular pattern of endosperm development, whose expression was inherited from that of the supernumerary embryo of the ancestors of flowering plants.     

Origins of flower morphology

Flowers evolved in many steps, probably starting long before flowering plants (angiophytes) originated. Certain parts of flowers are conservative and have not changed much during evolution; others are evolutionarily highly plastic. Here conservative features are discussed and an attempt is made to trace them back through their evolutionary history. Microsporangia and ovules (which develop into seeds) are preangiophyte floral elements. Angiospermy, combined with postgenital fusion, was the most prominent key innovation in angiophytes. Angiospermy and thecal organization of stamens originated earlier than all clades of extant angiosperms (the crown group of angiophytes). Differentiation of a perianth into calyx and corolla and syncarpy appeared after the first branching of the basalmost clades of extant angiosperms. Sympetaly and floral tubes as well as tenuinucellar, unitegmic ovules originated as major innovations in the clade that led to asterids. An obvious trend in flower evolution is increased synorganisation of parts, which led to new structures. Fixation of floral organ number and position was a precondition for synorganization. Concomitantly, plasticity changed from number and position of organs to shape of the new structures. Character distribution mapped onto cladograms indicates that key innovations do not appear suddenly, but start with trials and only later become deeply rooted genetically in the organization. This is implied from the common occurrence of reversals in the early history of an innovation. J. Exp. Zool. (Mol. Dev. Evol.) 291:105-115, 2001.     

腺齿木科系统位置评述

腺齿木科(Trimeniaceae)含2属5种。形态学研究显示腺齿木科具有许多原始性状。最新的分子系统发育研究显示,腺齿木科是现存被子植物的重要基部类群之一。但有关腺齿木科的系统位置存在争议。被子植物(有花植物)的起源与辐射一直是植物系统学家关注的热点。对该科系统位置的研究历史与现状进行评述。     

PhyloSort: a user-friendly phylogenetic sorting tool and its application to estimating the cyanobacterial contribution to the nuclear genome of Chlamydomonas

Background

Molecular phylogenetic analyses have identified Trimeniaceae, a monotypic family distributed only in Oceania, as among the earliest diverging families of extant angiosperms. Therefore, the fossils of this family are helpful to understand the earliest flowering plants. Paleobotanical information is also important to track the historical and geographical pathways to endemism of the Trimeniaceae. However, fossils of the family were previously unknown from the Early Cretaceous, the time when the angiosperm radiated. In this study, we report a seed from the late Albian (ca. 100 million years ago) of Japan representing the oldest known occurrence of Trimeniaceae and discuss the character evolution and biogeography of this family.

Results

A structurally preserved seed was collected from the early Late Albian Hikagenosawa Formation of the Yezo Group, which was deposited in palaeolatitudes of 35 to 40°N. The seed has a multilayered stony exotesta with alveolate surface, parenchymatous mesotesta, and operculate inner integument, which are characteristic to extant trimeniaceous seeds. However, the seed differs from extant seeds, i.e., in its well-developed endosperm and absence of antiraphal vascular bundle. Thus, the seed would be a new genus and species of Trimeniaceae.

Conclusion

The fossil seed indicates that seed coat characters were conserved for 100 million years or more in Trimeniaceae. It also suggests that the antiraphal vascular bundle and perispermy originated secondarily in Trimeniaceae as previously inferred from the phylogeny and character distribution in the extant basalmost angiosperms. The fossil seed provides the first evidence that Trimeniaceae was distributed in a midlatitude location of the Northern Hemisphere during the Early Cretaceous, when angiosperms radiated extensively, supporting a hypothesis that the extant austral distribution is relict.     

互叶梅科系统位置评述

互叶梅科 Amborellaceae 一属一种 .形态学研究显示互叶梅 Amborella tricopoda Baill. 具有许多原始性状 .大多数最新的分子系统发育研究显示 ,互叶梅科是现存被子植物的最基部类群 .但有关互叶梅科的系统位置存在争议 .被子植物 有花植物 的起源和辐射一直是植物学家关注的热点 .本文将对该科系统位置的研究历史与现状进行评述     

Perspective: the origin of flowering plants and their reproductive biology--a tale of two phylogenies

Recently, two areas of plant phylogeny have developed in ways that could not have been anticipated, even a few years ago. Among extant seed plants, new phylogenetic hypotheses suggest that Gnetales, a group of nonflowering seed plants widely hypothesized to be the closest extant relatives of angiosperms, may be less closely related to angiosperms than was believed. In addition, recent phylogenetic analyses of angiosperms have, for the first time, clearly identified the earliest lineages of flowering plants: Amborella, Nymphaeales, and a clade that includes Illiciales/ Trimeniaceae/Austrobaileyaceae. Together, the new seed plant and angiosperm phylogenetic hypotheses have major implications for interpretation of homology and character evolution associated with the origin and early history of flowering plants. As an example of the complex and often unpredictable interplay of phylogenetic and comparative biology, we analyze the evolution of double fertilization, a process that forms a diploid embryo and a triploid endosperm, the embryo-nourishing tissue unique to flowering plants. We demonstrate how the new phylogenetic hypotheses for seed plants and angiosperms can significantly alter previous interpretations of evolutionary homology and firmly entrenched assumptions about what is synapomorphic of flowering plants. In the case of endosperm, a solution to the century-old question of its potential homology with an embryo or a female gametophyte (the haploid egg-producing generation within the life cycle of a seed plant) remains complex and elusive. Too little is known of the comparative reproductive biology of extant nonflowering seed plants (Gnetales, conifers, cycads, and Ginkgo) to analyze definitively the potential homology of endosperm with antecedent structures. Remarkably, the new angiosperm phylogenies reveal that a second fertilization event to yield a biparental endosperm, long assumed to be an important synapomorphy of flowering plants, cannot be conclusively resolved as ancestral for flowering plants. Although substantive progress has been made in the analysis of phylogenetic relationships of seed plants and angiosperms, these efforts have not been matched by comparable levels of activity in comparative biology. The consequence of inadequate comparative biological information in an age of phylogenetic biology is a severe limitation on the potential to reconstruct key evolutionary historical events.     

Organization of the root apical meristem in angiosperms

Although flowers, leaves, and stems of the angiosperms have understandably received more attention than roots, the growing root tips, or root apical meristems (RAMs), are organs that could provide insight into angiosperm evolution. We studied RAM organization across a broad spectrum of angiosperms (45 orders and 132 families of basal angiosperms, monocots, and eudicots) to characterize angiosperm RAMs and cortex development related to RAMs. Types of RAM organization in root tips of flowering plants include open RAMs without boundaries between some tissues in the growing tip and closed RAMs with distinct boundaries between apical regions. Epidermis origin is associated with the cortex in some basal angiosperms and monocots and with the lateral rootcap in eudicots and other basal angiosperms. In most angiosperm RAMs, initials for the central region of the rootcap, or columella, are distinct from the lateral rootcap and its initials. Slightly more angiosperm families have exclusively closed RAMs than exclusively open RAMs, but many families have representatives with both open and closed RAMs. Root tips with open RAMs are generally found in angiosperm families considered sister to other families; certain open RAMs may be ancestral in angiosperms.     

Progress in Studies on Floral Development of Angiosperms and Some Consideration on Future Studies

With the advent of new methods and techniques, floral development has been ex tensively studied in many groups of angiosperms recently. These studies have resulted in notable progress and greatly increased our knowledge about the diversity of floral structure and developmental patterns as well as phylogenetic relationship of angiosperms. This field is be coming an active and exciting one in systematics of flowering plants. The present paper re viewed this progress from four aspects: (1) the methods of studies on floral development; (2) floral development and the diversity of floral structure; (3) floral development and phylogeny of angiosperms; (4) molecular genetics of floral development. In addition, several future directions and some problems needing attention in this field are discussed: (1) extensive studies on floral developmental studies of extensive species of angiosperms and comparison of floral structures among them; (2) research of floral development of homeotic flowers as well as their systematic and evolutionary value; (3) floral structure should be studied from the viewpoint of dynamics, because the structure of plants can be seen as a spatio-temporal pro- cess, and the use of structural categories in systematics may distort the natural dynamics.     

被子植物系统学中花发育研究的进展及对今后研究的思考

从花发育研究的方法、花发育与被子植物花部结构的多样性、花发育与被子植物的系统发育以及 花发育的分子遗传学等四个方面对近年来被子植物系统学中花发育研究的主要进展作一综述,例举了 一些重要结果。同时,对该领域今后研究的方向和应注意的一些问题作了简要评论。作者认为植物的 形态结构可以看作是一个时空过程,在系统学研究中对花部性状的分析和认识应该树立动态的观点。 今后应该从动态的角度开展被子植物花的发生和发育以及性状在不同类群间的比较等方面的广泛研究,并加强对在被子植物花的起源和演化中起重要作用的花部同源异型现象的发育过程的观察。     

A phylogenetic classification of the land plants to accompany APG III

A formal classification of the land plants that is compatible with the APG III classification is proposed. Previous classifications inflated taxonomic ranks, particularly of the angiosperms. If the major clades of green algae are recognized as classes, then all land plants, the embryophytes, should be included in a single class, here recognized as Equisitopsida. Accordingly, the 16 major clades of land plants, including the angiosperms, should all be recognized as subclasses, the angiosperms as Magnoliidae. Major clades within the angiosperms are then recognized as superorders. This classification still uses a few informal categories (e.g. eudicots, lamiids, etc.) within the angiosperms because this is convenient. Two new names are established: Amborellanae and Austrobaileyanae. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 161 , 122–127.     

An exceptional role for flowering plant physiology in the expansion of tropical rainforests and biodiversity

Movement of water from soil to atmosphere by plant transpiration can feed precipitation, but is limited by the hydraulic capacities of plants, which have not been uniform through time. The flowering plants that dominate modern vegetation possess transpiration capacities that are dramatically higher than any other plants, living or extinct. Transpiration operates at the level of the leaf, however, and how the impact of this physiological revolution scales up to the landscape and larger environment remains unclear. Here, climate modelling demonstrates that angiosperms help ensure aseasonally high levels of precipitation in the modern tropics. Most strikingly, replacement of angiosperm with non-angiosperm vegetation would result in a hotter, drier and more seasonal Amazon basin, decreasing the overall area of ever-wet rainforest by 80 per cent. Thus, flowering plant ecological dominance has strongly altered climate and the global hydrological cycle. Because tropical biodiversity is closely tied to precipitation and rainforest area, angiosperm climate modification may have promoted diversification of the angiosperms themselves, as well as radiations of diverse vertebrate and invertebrate animal lineages and of epiphytic plants. Their exceptional potential for environmental modification may have contributed to divergent responses to similar climates and global perturbations, like mass extinctions, before and after angiosperm evolution.     

Variation in the phenology and abundance of flowering by native and exotic plants in subalpine meadows

The timing and abundance of flower production is important to the reproductive success of angiosperms as well as pollinators and floral and seed herbivores. Exotic plants often compete with native plants for space and limiting resources, potentially altering community floral dynamics. We used observations and a biomass-removal experiment to explore the effects of an invasive exotic flowering plant, Linaria vulgaris, on community and individual species flowering phenology and abundance in subalpine meadows in Colorado, USA. Invasion by L. vulgaris was associated with a shift in both the timing and abundance of community flowering. Invaded plant communities exhibited depressed flowering by 67% early in the season relative to uninvaded communities, but invaded sites produced 7.6 times more flowers than uninvaded sites once L. vulgaris began flowering. This increase in flowers at the end of the season was driven primarily by prolific flowering of L. vulgaris. We also found lower richness and evenness of resident flowering species in invaded plots during the period of L. vulgaris flowering. At the species level, a common native species (Potentilla pulcherrima) produced 71% fewer flowers in invaded relative to uninvaded plots, and the species had reduced duration of flowering in invaded relative to uninvaded sites. This result suggests that L. vulgaris does not simply alter the flowering of subordinate species but also the flowering of an individual common species in the plant community. We then used observational data to explore the relationship between L. vulgaris density and resident floral production but found only partial evidence that higher densities of L. vulgaris were associated with stronger effects on resident floral production. Taken together, results suggest that a dominant invasive plant can affect community and individual-species flowering.