Morphological studies on the genusClematis linn

In four-sepaled flowers ofClematis the sepal is supplied by three main traces. The basic pattern of the vascular supply to sepals is found inC. alpina var.ochotensis which invariably has six-bundled pedicels. It is as follows: the median traces to the first pair of opposite sepals, as well as all the lateral traces, arise directly from pedicel bundles, while those to the second pair are formed secondarily, after fusion and subsequent division of two adjacent pedicel bundles. As to the manner of origin of the median traces, the pattern is similar to that of the vascular supply to foliage leaves. This gives further evidence for the generally accepted view that the sepals ofClematis, like foliage leaves, are decussately arranged. In most other species such asC. apiifolia, C. stans, etc. the number of pedicel bundles tends to be reduced from six to four so as to coincide with that of the sepals, so patterns are much simplified and specialized: all the traces arise directly from pedicel bundles. InC. japonica an iconsistent pattern is observed, since the number of pedicel bundles from which sepal traces arise is much higher and varied.     

Morphological studies on the genusClematis linn. VIII. Floral and inflorescence anatomy inClematis patens with eight-sepaled flowers

The vascular anatomy of inflorescence axes and flowers ofClematis patens have been studied. The species shows a unique behaviour of the vascular bundles in the transition node from vegetative stem to pedicel: stelar bundles increase in number from six to eight as they ascend through the transition node so that the number of vascular bundles coincides with that of sepals. In the pedicel stele the resulting eight bundles are disposed opposite to eight sepals. respectively; each sepal receives its vascular supply from the bundle facing it. Morphological and anatomical evidence suggests that the calyx of eight sepals in this species should be interpreted as having consisted originally of four pairs of opposite organs, rather than as having been derived secondarily through chorisis of sepals from a calyx of four sepals as seen in most other species ofClematis.     

Anomalous secondary vascular tissue inHelminthostachys zeylanica (Ophioglossaceae)

The vascular anatomy ofHelminthostachys zeylanica was examined with special reference to anomalous secondary tissue. Primary xylem development gradually takes place centrifugally. In branched rhizomes with destroyed apices, the vascular cylinder apical to the insertion of branch traces is generally composed of primary xylem, accessory xylem, inner parenchyma of radially arranged cells, outer parenchyma of irregularly arranged cells, and partly crushed phloem, listed in order going outwards. The accessory xylem as well as the inner parenchyma ofHelminthostachys zeylanica is probably secondarily produced, partly to contribute to the branch traces, in a position corresponding to that of secondary vascular tissue developed from a normal cambium inBotrychium sensu lato. It is suggested that although a cambium is lacking inHelminthostachys zeylanica, the secondary vascular tissues are comparable between the genera. The phylogenetic implication of this tissue is discussed.     

Floral anatomy ofCamellia japonica (Theaceae)

The floral anatomy ofCamellia japonica is described and the origin of its multistaminate androecium is considered. Of significance is the observation that the complex polyandry of the genus overlies a basic vascular obdiplostemonous pattern. This is evidenced by two systems of staminal bundles. The first diverges from a set of five common petal-stamen bundles and subsequently divides further. The second set of five staminal trunk bundles emerges from the central cylinder slightly above the petal-stamen bundles which are antepetalous. The observations will aid phylogenetic reconstruction for members of the polyphyletic order Dilleniidae to whichCamellia belongs, and in which the polyandry has been too simply and sometimes incorrectly interpreted as a primitive condition.     

Comparative studies of the vascular system of node-leaf continuum in woody ranales

The vascularization of the node-leaf continuum in the first to eighth foliage leaves of the first-year plant ofMagnolia virginiana is investigated. The cotyledonary node is a 4-trace, 3-lacunar type. Vascularization in the cotyledonary node is fundamentally different from that in the folair node of the same plant. As a result, the cotyledonary vascularization is only described but not compared to that in the foliar node-leaf continuum. Considerable diversity occurs in the node-leaf vascularization of the first-year plants. A 5-trace, 4-lacunar vascular system is constant in the lower folair nodes; this is considered to be the fundamental vascular pattern in the node-leaf continuum of the species. In contrast, the nodal anatomy and petiolar vascularization fluctuate widely in the third to eighth leaves of the first-year plants. Variation is found not only between different nodes of a single plant but even in the corresponding nodes of different individuals. The evidence clearly indicates that variation always correlates with certain members of the leaf-trace complement; thus, either the ventral and/or marginal lateral bundles undergo phylogenetical reduction or amplification.     

The morphology and anatomy ofHydrastis (Ranunculales): Systematic reevaluation of the genus

Evidence from morphology and anatomy (including embryology), as well as from palynology, chemistry and cytology, indicates thatHydrastis is quite divergent from Ranunculaceae (in which the genus has been most often included) as well as from both Glaucidiaceae and Berberidaceae. Distinctive features ofHydrastis, which demarcate it from Ranunculaceae but which are sometimes shared by Berberidaceae, are: the unique mode of origin of the vascular supply to stamens and carpels; the micropyle being formed by both integuments; the xylem not V-shaped in cross section; scalariform vessel perforations present; haploid chromosome number 13; pollen tectum consisting of a compound layer of striae; leaf mesophyll not differentiated; the unique course of stem medullary bundles; D-galactose present. Its distinctive higher haploid chromosome number, as well as its many less-specialized character states (in floral structure, leaf anatomy, and xylem and vessel morphology), suggest thatHydrastis is a relictual primitive group which diverged early from a common ancestral stock of Ranunculaceae, Berberidaceae and probably of Circaeasteraceae; at least some of the features shared byHydrastis and one or another of the families concerned seem to be a heritage from their common ancestor. We propose a reestablishment of a monotypic family, Hydrastidaceae.     

Morphological studies on the genusClematis Linn

The basic pattern of the vascular supply to stamens and carpels in the flowers ofClematis is discussed on the basis of serial sections. The bundles of the receptacular stele show fairly regular fusions and divisions in relation to the origin of the vascular supply, giving off a single trace for each stamen or carpel. In many cases the trace arises by the trifurcation of the “fused bundle” and the subsequent departure of the median strand. This is the pattern basic to the structure of the receptacular stele of the genus. Although the basic pattern involves a variety of modifications, each of the diverging traces fundamentally leaves a single independent gap in the stele, contrary to the conclusion of previous authors. Similarities and differences between a group of stamens and carpels and that of sepals and foliage leaves are also discussed based on the results of the present and previous studies on the vascular anatomy of the floral receptacle and the inflorescence axis.     

Observations on bipolar disjunctions of moonwort ferns (Botrychium,Ophioglossaceae)

Peter Raven, in 1963, included two fern taxa of the genus Botrychium in his list of plant species exhibiting American amphitropical bipolar disjunctions. He attributed the southern hemisphere occurrences to post‐Pleistocene long‐distance dispersal from counterparts in the northern hemisphere, probably assisted by annual bird migrations between the disjunct areas. Using genetic evidence gathered through worldwide analyses of phylogenetic relationship in Botrychium, we now review and reconsider Raven's conclusions. Genetic similarities indicate that South American Botrychium dusenii is an allotetraploid taxon closely related to B. spathulatum, a North American endemic, and that B. lunaria in New Zealand possesses a genotype identical to that of a taxon in North America derived through introgressive hybridization between B. lunaria and an endemic North American species, B. neolunaria. Both North American counterparts exhibit Raven's characteristics of bipolar disjuncts in their occurrence in mountain and coastal meadows, copious production of small propagules (spores in Botrychium), occurrence in habitats frequented by transpolar bird migrants, and ability to found new colonies through inbreeding. We discuss these characteristics in Botrychium and relative to other ferns and suggest further studies on Botrychium and related taxa to address questions of time, number, and mode of bipolar dispersals.     

Isozyme variability among cryptic species of Botrychium subgenus Botrychium (Ophioglossaceae)

The systematics of Botrychium subgenus Botrychium has been controversial, primarily because reduction in frond size and complexity has limited the number of characters available for discrimination of species. The recognition of many polyploid species has magnified the difficulty of classification because allopolyploids are often morphologically intermediate between their progenitor diploids. In order to evaluate species limits and sectional boundaries, we surveyed and compared 16 of the 24 currently recognized species for isozymic variation. Little or no intrapopulational variation was detected, but the variation present was consistent with the hypothesis that Botrychium species are primarily inbreeding. Interspecific comparisons distinguished six diploid species and provided evidence of molecular differentiation between the cryptic sister species B. lunaria and B. crenulatum. Evidence of possible progenitor/descendant relationships was found for certain diploid/polyploid relationships. Using enzyme bands shared between species, realignment of the sectional assignment of several species is proposed. Anomalous banding patterns in certain individuals suggested that gene silencing or homoeologous chromosome pairing might be operating in B. minganense, B. hesperium, and B. matricariifolium. Isozyme data also showed that some populations of species presumed to be uniformly diploid possessed isozyme patterns typical of polyploids. All available molecular data indicate that members of Botrychium subgenus Botrychium are actively evolving at diploid and polyploid levels.     

Inverted vascular bundles in the leaf of Cladium (Cyperaceae)

Illustrations of seedling development and the adult plant of Cladium jamaicense Crantz are given. The course of vascular bundles in the leaf is described in detail. The structure of seedling and adult leaves are compared. Development of leaf primordia and initiation of vascular bundles are followed. Changes in the anatomy within one leaf and differences between foliage leaves and scales are related to their development. The adaxial vascular bundles that are inversely orientated are initiated within a procambial complex in close association with the largest abaxial bundles. Normally orientated adaxial bundles have an origin independent of other bundles. A hypothesis is presented which accounts for the differentiation of inverted bundles in morphogenetic terms. No developmental evidence was found to support the phylogenetic derivation of the leaf of Cladium by adaxial folding and fusion of laminar halves with their own adaxial surfaces.     

Vegetative morphology and anatomy of Maundia (Maundiaceae: Alismatales) and patterns of peripheral bundle orientation in angiosperm leaves with three‐dimensional venation

Collateral bundles with external position of the phloem characterize the stem vasculature of most seed plants. An earlier study highlighted the occurrence of inverted peripheral bundles in the leafless inflorescence peduncle of the rare Australian aquatic Maundia triglochinoides. This unusual feature and other morphological and molecular data supported the recognition of the monogeneric Maundiaceae, but the anatomy of the leaves, rhizomes and roots of Maundia remained unknown and is studied here. Maundia has an iterative sympodial growth with all shoots bearing five tubular cataphylls splitting longitudinally and simulating open sheaths at maturity and two (or three) linear foliage leaves without a conspicuous basal sheath. This morphology distinguishes Maundiaceae from all other Alismatales. The rhizome has an atactostele with collateral bundles of normal orientation; peripheral bundles are absent. Cataphylls have a series of normally oriented bundles. Foliage leaves are thick, bifacial, semi‐elliptical in cross‐section, with a thin subepidermal layer of chlorenchyma on both sides, accompanied by peripheral bundles with xylem facing outwards (thus abaxial peripheral bundles are inverted) and central large bundles of normal orientation. Strong anatomical similarity between leaves and peduncles is related to their shared function as assimilatory organs. As in angiosperm succulents, the three‐dimensional leaf venation in thick aquatic and helophyte leaves of Alismatales serves to reduce transport distances between veins and photosynthetic cells. In both cases, the patterns of orientation of peripheral bundles (with inverted adaxial or abaxial bundles) are unstable in large clades. These slender bundles cannot be used for the identification of unifacial leaves. Some anatomical characters express homoplastic similarities between Maundiaceae and Aponogetonaceae.     

单芽狗脊营养器官的解剖学研究

采用离析法和石蜡切片法对单芽狗脊营养器官进行形态解剖研究。结果表明：单芽狗脊叶为异面叶,上、下表皮细胞均为不规则型,仅下表皮有气孔器分布;叶柄维管束有2~6个,自叶柄基部向上至叶轴仅有2个较大的维管束;根状茎薄壁细胞之间有多个维管束散生分布,且富含丰富的淀粉粒;皮层在根的横切结构中占比较大,木质部的发育方式为外始式;单芽狗脊珠芽的发育过程分为三个阶段,珠芽原基的形成期、珠芽原基的分化期、成熟期。     

Comparative vegetative anatomy and systematics of Laeliinae (Orchidaceae)

Laeliinae are one of the most prominent orchid subtribes, with c. 40 genera and nearly 1500 species, and contain a disparate group of taxa with widely varying morphological features. There does not appear to be a complex of characters to which one can refer in order to delineate the subtribe as a whole. Thus, it was thought that vegetative anatomy might provide clues to the monophyly of the group. The microscopic structure of the leaves, stems and roots of representatives of most of the genera was studied. It was concluded that the anatomy lacks overall uniformity and that vegetative characters alone are insufficient to assess the relationships amongst the genera. The only nearly consistent anatomical feature was the abaxial row of fibre bundles in the leaves. Thus, anatomically, as well as morphologically, Laeliinae are a mixed bag. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 21–41.     

Androecium and floral nectaries ofHarungana madagascariensis (Clusiaceae)

The mature flower ofHarungana madagascariensis (Choisy)Poir. has an androecium of five antipetalous fascicles, consisting of four stamens each. The stamen fascicles alternate with five indented nectary scales. A SEM-study of the floral development, as well as a study of the floral anatomy was carried out to understand whether the nectariferous scales represent staminodia or are receptacular in nature and consequently whether or not the androecium ofHarungana, and theClusiaceae in general, is originally diplostemonous. The five petals originate by the splitting of petal-stamen complexes. Next the upper part of each complex differentiates basipetally in four stamens. The stamens remain fascicled and are lifted on a long stalk at maturity. Five carpel primordia are initiated united in a low ringwall. The five nectary scales appear after carpel inception and develop an external morphology reminiscent of anthers. The floral anatomy reveals an independent origin of sepal median traces and common sepal lateral traces, free petal traces, stamen fascicle traces and alternating vascular tissue which supplies the nectaries. The petal-stamen complexes are the result of a retardation in petal inception, linked with the absorption of petal tissue into the stamen primordia. The development of the stamen fascicles is discussed; it is suggested that they are of a secondary nature and do not appear as a reduction from a multistaminate androecium. The external morphology and vascular anatomy of the scales speaks in favour of a staminodial nature. The comparison with some other species of theClusiaceae gives evidence of a diplostemonous ancestry of the androecium.     

Taxonomic studies ofAsarum sensu lato

The floral vascular anatomy of 12 species representing each ofAsarum s. str.,Asiasarum, Geotaenium, Heterotropa andHexastylis are compared to clarify intergeneric relationships. The five genera have basically similar structures in floral morphology and vasculature, and consistently have a six-carpelled compound ovary and the associated similar placental vasculature. They show, however, a significant difference in the position and the constituent of the “ventral” carpellary bundles in the placental axis betweenAsiasarum-Heterotropa-Hexastylis andAsarum-Geotaenium. InAsiasarum, Heterotropa andHexastylis the ventral bundles of each carpel are basically free and antilocular as expected in the least specialized compound ovary of angiosperms; in contrast, inAsarum andGeotaenium the ventral carpellary bundles are antiseptal and heterogenous (i.e., formed by the lateral fusion of ventral bundles of adjacent carpels). Shared probable apomorphic floral vasculature, as well as shared single style-column, suggests the closest mutual relationships betweenAsarum andGeotaenium. In terms of floral morphology and anatomy,Asiasarum, Heterotropa andHexastylis retain plesiomorphies. Possible chromosomal evolution in the related genera is also discussed.     

Vascular floral anatomy of the east asianHeloniopsis orientalis (Thunb.) C. Tanaka (Liliaceae-Helonieae)

Observations on the vascular floral anatomy, carpel morphology and floral biology ofHeloniopsis orientalis are presented. The lower flowering pedicel has six large bundles which lack an enclosing sclerenchymatous sheath. At mid-pedicel, branch bundles originate via radial divisions from each of these bundles. Subsequently, there is a vascular ring of 12 bundles below the receptacle. The six smaller bundles which are derived from alternate pedicel bundles eventually establish all of the ventral gynoecium supply. The six larger bundles supply the tepals, stamens and dorsal gynoecial vasculature. The simple dorsals do not branch or fuse in their vertical ascent. The ventral and placental supplies are far more complex. Fusion occurs between paired sets of the six smaller pedicel bundles along the septal radii and results in a submarginal laminal ventral network. An independent ventral plexus is formed in each septum and from each plexus two septal axials, of which the innermost has a reversed xylem-phloem disposition, and four placental bundles are derived. Two placental bundles are associated with each septal axial. Basally the septa are fused centrally, but are freed at mid-gymoecial height. The broadly tri-lobed, tri-carpellate gynoecium is depressed terminally where the erect, hollow style with its capitate stigma is attached. Dorsal grooves are present: the fruit is loculicidally dehiscent. There are no septal glands due to complete lateral fusion of the septal wings. Basally each of the six equal tepals has a saccate nectary. The similarity in vascular anatomy and carpel morphology of the AsianHeloniopsis and eastern North American endemic,Helonias bullata, justifies their position in the same tribe. Research and publication supported in part by the M. Graham Netting Research Fund through a grant from the Cordelia Scaife May Charitable Trust, the U. S.—Japan Cooperative Science Program Grant GF-41367, the Japan Society for the Promotion of Science, and Grant-in-Aid No. 934053 from the Ministry of Education, Japan.     

Anatomy and systematics of Dendroseris (sensu lato)

Anatomical study of the genusDendroseris (Compositae: Cichorieae), endemic to the Juan Fernandez Islands, was undertaken to determine if segregate genera were valid. Other questions include the significance of pith bundles and of receptacular bristles, and whether the ancestors of these peculiar rosette trees and shrubs were woody or herbaceous. Anatomical evidence, when added to that from gross morphology, suggests that the segregation as distinct genera ofRea, Phoenicoseris, andHesperoseris is probably not justified, and that they are better treated as subgenera ofDendroseris. Differences in pollen morphology, floral trichomes, achene and leaf anatomy provide good species characteristics. These all appear, respectively, as variations on a basic plan, andDendroseris can be envisaged as derived from a common stock in the Juan Fernandez Islands. The genus is not particularly primitive within the family or tribe. The presence of additional bundles in the flowers ofD. litoralis may be interpreted as related to gigantism. The separate corolla lobes inD. gigantea probably do not represent a vestige of an actinomorphic condition. Pith bundles inDendroseris may have been present in ancestors; in any case, they seem likely to have increased in prominence with increase in stem diameter. Available evidence seems to favor the interpretation of growth forms inDendroseris as derived from an herbaceous ancestry.     

The uptake of3H-thymidine and its transport inDatura stramonium L.

Exogenous³H-thymidine is absorbed by the primary root of young plants ofDatura stramonium L. and gradually translocated into shoots: following a 3 to 72-h application of³H-thymidine the radioactivity was revealed, using the autoradiographic technique, especially in the region of primary and secondary meristems and in proximity to vascular bundles of the primary root, stem, hypocotyl and leaves. These regions may be considered as the sites of active DNA synthesis. The intensity of incorporation was dependent on the time of plant incubation in labelled thymidine.     

THE ORGANIZATION OF THE VASCULAR SYSTEM IN THE STEMS OF THE NYMPHAEACEAE. II. NYMPHAEA SUBGENERA ANECPHYA,LOTOS, AND BRACHYCERAS

The anatomy and organization of the stem vascular system was analyzed in representative taxa of Nymphaea (subgenera Anecphya, Lotos, and Brachyceras). The stem vascular system consists of a series of concentric axial stem bundles from which traces to lateral organs depart. At the node each leaf is supplied with a median and two lateral leaf traces. At the same level a root trace supplies vascular tissue to adventitious roots borne on the leaf base. Flowers and vegetative buds occupy leaf sites in the genetic spiral and in the parastichies seen on the stem exterior. Certain leaves have flowers related to them spatially and by vascular association. Flowers (and similarly vegetative buds) are vascularized by a peduncle trace that arises from a peduncle fusion bundle located in the pith. The peduncle fusion bundle is formed by the fusion of vascular tissue derived from axial stem bundles that supply traces to certain leaves. The organization of the vascular system in the investigated taxa of Nymphaea is unique to angiosperms but similar to other subgenera of Nymphaea.     

Some features of secretory systems in plants

Synopsis Recent work on secretion in plants is reviewed, with emphasis on the anatomy and physiology of root cap cells in higher plants, the stalked glands ofDrosera capensis, and the secretory mechanism ofDionaea muscipula. Cells of the root cap of higher plants switch from a geo-perceptive role to one of mucilage secretion at maturation. Features of this process, the role of the Golgi and the pathway for mucilage distribution are reviewed. In contrast, the stalked glands of the leaves ofDrosera capensis are much longer lived and have a complex anatomy. The mechanisms for mucilage secretion, protein absorption and the role of the cell membranes in the internal secretion of the protein are described, using data from X-ray microscopv. The secretion of fluid and protein byDionaea is stimulated by various nitrogen-containing compounds. Uric acid, often excreted by captured insects, is particularly effective in this respect.