<Emphasis Type="Italic">Scleria rubrostriata,</Emphasis> a new species of Cyperaceae from the Brazilian Atlantic Forest

A new species is here described: Scleria rubrostriata A. C. Araújo & N. A. Brummitt, a herb from the Atlantic forest of Espírito Santo State, south-eastern Brazil. A key to the sections of Scleria and to the American species of Scleria sect. Schizolepis is provided, and an illustration of the new species and comparison to similar taxa are given.     

Diversity of inflorescences in the Boutelouinae subtribe (Poaceae: Chloridoideae: Cynodonteae)

The Boutelouinae subtribe is comprised of one monophyletic genus, Bouteloua, with 57 species inhabiting the semi-arid regions of the New World. The inflorescences show significant structural variations, which provides an interesting system to examine their morphological evolution and identify characters and processes that may help to understand the group systematics. The structure of inflorescences was studied in 25 species of Bouteloua. All the species covered under this study have truncated polytelic inflorescences. Structural variations in the inflorescence unit among species may be accounted for by: (1) symmetry of the inflorescence unit, (2) total number of long primary branches, (3) total number of spikelets per branch, (4) number of perfect flowers per spikelet, (5) number of rudimentary flowers, and (6) reproductive system. Homogenization and truncation processes account for the diversity of mature inflorescences that exists in Bouteloua. In this work, we discuss the systematic and taxonomic value of the inflorescence in the Boutelouinae subtribe.     

Variation in scent emission among floral parts and inflorescence developmental stages in beetle-pollinated Protea species (Proteaceae)

Floral fragrances are an important component for pollinator attraction in beetle-pollinated flowers. Several genera in the Proteaceae contain beetle-pollinated species. However, there is no information on the floral scent chemistry of beetle-pollinated members of the family. In this paper we report on the spatial variation and differences between developmental stages in emission of inflorescence (flowerhead) volatiles of four South African Protea species (P. caffra, P. dracomontana, P. simplex, and P. welwitschii) that are pollinated by cetoniine beetles. The scents from different inflorescence parts (bracts, perianth, styles, and nectar) and from successive anthesis stages of whole inflorescences were sampled using dynamic headspace collection and identified using GC–MS. Although the four species shared many scent compounds, possibly reflecting their close phylogenetic relationships and common pollinators, they showed significant differences in overall scent composition due to various species-specific compounds, such as the unique tiglate esters found in the scent of P. welwitschii. The strongest emissions and largest number of volatiles, especially monoterpenes, were from inflorescences at full pollen dehiscence. Senescing inflorescences of two species and nectars of all species emitted proportionally high amounts of acetoin (3-hydroxy-2-butanone) and aromatic alcohols, typical fermentation products. As a consequence, the scent composition of nectar was much more similar among species than was the scent composition of other parts of the inflorescence. These results illustrate how the blends of compounds that make up the overall floral scent are a dynamic consequence of emissions from various plant parts.     

云南的珍珠茅属植物

对产于云南省的珍珠茅属植物进行了分类学修订。作者确认了产于云南的珍珠茅属植物12种,修正了5个种错误的学名,另有1个种被并入其它种为异名。在12种有2种为产于云南的新记录。文中包括云南珍珠茅属的分种检索表、各种的分类学处理及地理分布。     

Inflorescence structure in species of Spartina Schreb. (Poaceae: Chloridoideae: Cynodonteae)

The typology developed by Troll was followed to describe inflorescence structures for 15 species of Spartina. In all species here studied, truncation of the terminal spikelet of the main axis and primary paracladium was observed. The truncation can also involve the short paracladia subzone so that the inflorescence is confined to just the long paracladia subzone. A great homogenization of paracladia and maximum ramification degree limited generally to the second order of branching are distinctive characteristics of the genus. Proximal paracladia with third-order branching were found in only three specimens, and in these exceptional cases, the homogenization is partial. Sometimes, in some species, a subzone of long and short paracladia can be distinguished. The absence of trophotagma paracladia in all the species studied was verified. The variation in the structure of the inflorescence among species is due to the differences in the number of short paracladia, long paracladia, total number of primary paracladia and also in the angle of divergence of the long paracladia from the main axis. The latter, in addition to variations in the intercalary growth of the internodes produces modifications in the general appearance of the inflorescences. The systematic and taxonomic value of the inflorescences in Spartina is discussed.     

Testing the ontogenetic base for the transient model of inflorescence development

Backgrounds and Aims

Current research in plant science has concentrated on revealing ontogenetic processes of key attributes in plant evolution. One recently discussed model is the ‘transient model’ successful in explaining some types of inflorescence architectures based on two main principles: the decline of the so called ‘vegetativeness’ (veg) factor and the transient nature of apical meristems in developing inflorescences. This study examines whether both principles find a concrete ontogenetic correlate in inflorescence development.

Methods

To test the ontogenetic base of veg decline and the transient character of apical meristems the ontogeny of meristematic size in developing inflorescences was investigated under scanning electron microscopy. Early and late inflorescence meristems were measured and compared during inflorescence development in 13 eudicot species from 11 families.

Key Results

The initial size of the inflorescence meristem in closed inflorescences correlates with the number of nodes in the mature inflorescence. Conjunct compound inflorescences (panicles) show a constant decrease of meristematic size from early to late inflorescence meristems, while disjunct compound inflorescences present an enlargement by merging from early inflorescence meristems to late inflorescence meristems, implying a qualitative change of the apical meristems during ontogeny.

Conclusions

Partial confirmation was found for the transient model for inflorescence architecture in the ontogeny: the initial size of the apical meristem in closed inflorescences is consistent with the postulated veg decline mechanism regulating the size of the inflorescence. However, the observed biphasic kinetics of the development of the apical meristem in compound racemes offers the primary explanation for their disjunct morphology, contrary to the putative exclusive transient mechanism in lateral axes as expected by the model.     

Morphology and anatomy of inflorescence and inflorescence axis in Paepalanthus sect. Diphyomene Ruhland (Eriocaulaceae,Poales) and its taxonomic implications

Paepalanthus sect. Diphyomene has inflorescences arranged in umbels. The underlying bauplan seems however to be more complex and composed of several distinct subunits. Despite appearing superficially very similar, the morphology and anatomy of the inflorescences can supply useful information for the understanding of the phylogeny and taxonomy of the group. Inflorescences of Paepalanthus erectifolius, Paepalanthus flaccidus, Paepalanthus giganteus, and Paepalanthus polycladus were analyzed in regard to branching pattern and anatomy. In P. erectifolius, P. giganteus and P. polycladus the structure is a tribotryum, with terminal dibotryum, and with pherophylls bearing lateral dibotrya. In P. flaccidus, the inflorescence is a pleiobotryum, with terminal subunit, and without pherophylls. Secondary inflorescences may occur in all species without regular pattern. Especially when grown in sites without a pronounced seasonality, the distinction between enrichment zone (part of the same inflorescence) and new inflorescences may be obscured. The main anatomical features supplying diagnostic and phylogenetic information are as follows: (a) in the elongated axis, the thickness of the epidermal cell walls and the cortex size; (b) in the bracts, the quantity of parenchyma cells (c) in the scapes, the shape and the presence of a pith tissue. Therefore, P. sect. Diphyomene can be divided in two groups; group A is represented by P. erectifolius, P. giganteus and P. polycladus, and group B is represented by P. flaccidus. The differentiation is based in both, inflorescence structure and anatomy. Group A presents a life cycle and anatomical features similar to species of Actinocephalus. Molecular trees also point that these two groups are closely related. However, inflorescence morphology and blooming sequence are different. Species of group B present an inflorescence structure and anatomical features shared with many genera and species in Eriocaulaceae. The available molecular and morphology based phylogenies still do not allow a precise allocation of the group in the bulk of basal species of Paepalanthus collocated in P. sect. Variabiles. The characters described and used here supply however important information towards this goal.     

THE MORPHOLOGY AND RELATIONSHIPS OF DALECHAMPIA SCANDENS (EUPHORBIACEAE)

The circumtropical but preponderantly American genus Dalechampia, comprising nearly 100 species of twining vines (or rarely subshrubs), is strikingly isolated within the Euphorbiaceae because of its distinctive bibracteate inflorescences. There has been considerable taxonomic controversy with regard to the relationships of the genus, and it has been suggested that Dalechampia is allied to the tribe Euphorbieae because of a supposed analogy between its inflorescence and the cyathium in the Euphorbieae. Field and laboratory investigations of the common American species D. scandens, together with a comparative survey of related species, have thrown some light on these problems. The Dalechampia inflorescence seems best interpreted as consisting of a terminal staminate pleiochasium (with part of the lateral branches transformed for nectar production), juxtaposed to a 3-flowered pistillate cyme. The lips of the conspicuous bilabiate involucre are formed by the hypertrophied bracts which subtend the staminate and pistillate cymes. The bisexual inflorescences appear to be distinctly proterogynous, rather than proterandrous, as has been previously suggested. The configuration of the inflorescence—a bilaterally symmetrical pseudanthium—suggests adaptation for crosspollination, but the closing movement of the bracts makes self-pollination probable in the absence of visits by pollinators. The similarity of the Dalechampia inflorescence to the cyathium of the Euphorbieae appears to be entirely superficial, and both reproductive and vegetative data suggest that Dalechampia is related to taxa of tribe Plukenetieae.     

Developmental morphology of the Asian one-leaf plant, Monophyllaea glabra (Gesneriaceae) with emphasis on inflorescence morphology

We examined the developmental morphology of the tropical Asian one-leaf plant Monophyllaea glabra, which is believed to have diverged first in the phylogenetic tree of the genus. The embryo within the seed consists of two cotyledons and a hypocotyl with no shoot or root apical meristems. The endogenous root meristem is formed nearer the hypocotyl end than in other examined Monophyllaea species. One of the cotyledons grows to form the macrocotyledon by means of the basal meristem. The groove meristem arises between the anisocotyledons, shifts toward the macrocotyledon, and is transformed to the inflorescence apex, which produces inflorescence axes in the axils of all ventral bracts of two rows, and secondary inflorescences in the axils of the lower dorsal bracts of the other two rows. The macrocotyledon may act as a ventral bract for the first inflorescence axis at the reproductive stage. This organization suggests that a common ancestor of Monophyllaea and Whytockia with decussate inflorescences diverged in one direction to become Monophyllaea and in another to become Whytockia.     

Studies in African Cyperaceae 29. Scleria afroreflexa, a new species from western Cameroon

A new rare species, Scleria afroreflexa. is descriped from an upland area (1500 m) of South west Cameroon. It is most similar to S. sheilae Rayn., another rare species only known from one collection from a rocky habitat at 800 m near Yaounde in southeastern Cameroon. S. afroreflexa differs, however, in its more dense inflorescence with reflexed branches, its more hairy leaves, smaller achenes and in its montane habitat. Notes on habitat, ecology, distribution and conservation are given for the two species.     

Phylogeny of the Southeast Asian endemic genus Neocinnamomum H. Liu (Lauraceae)

A phylogenetic analysis of Neocinnamomum H. Liu and related genera was conducted using psbA–trnH, trnK cpDNA regions, and the ITS nrDNA segment. Neocinnamomum was confirmed to be monophyletic, and an evolutionary series of inflorescence development within the genus was recognized. The compound thyrse seen in N. caudatum is reduced to the few- to many-flowered condensed inflorescences with a poorly defined branching system seen in most species and ultimately to the 1-flowered inflorescence seen in N. atjehense. Consensus network analysis (CNA) suggested that long-branch attraction is responsible for the observed close relationship between Neocinnamomum and Cassytha L. in a combined analysis of the complete data. In contrast, the sister relationship of Neocinnamomum and Caryodaphnopsis seen in the Bayesian analyses of the partial combined matrix was supported by CNA and is also supported by morphology and wood and bark anatomy. The close similarity of the compound thyrse of less derived Neocinnamomum species to the thyrsoid inflorescences of some Caryodaphnopsis species is also seen as strong support for their affinity.     

国产耳草属长节耳草及其相似种的分类研究

我国耳草属中具有茎四棱和头状花序特征的植物常常被鉴定为长节耳草(Hedyotis uncinella),并且这一名称还包括了基于不同模式的3个分类学异名。由于这一类植物在叶片形态、叶柄长短、花序着生式样以及花梗长度等形态特征方面存在着明显的不同,因此将这一类植物笼统地鉴定为长节耳草并不合理。为清晰区分这类植物,通过模式比对、居群形态特征变异式样的野外观察以及分子系统学分析等方法进行研究,结果表明,以前被鉴定为“长节耳草”的植物实际上包括了6个分类实体,即被归并的丰花耳草(H. borrerioides)、垦丁耳草(H. kuraruensis)和新组合种——团花耳草(H. cephalophora)均应独立成种,而长节耳草本种、被忽略的线叶耳草(H. linearifolia)和我国新记录种——球花耳草(H. multiglomerulata)各自也应得到承认。同时,为了便于进行分类鉴定,也提供了这些种类的分种检索表。     

Floral display size in comfrey, Symphytum officinale L. (Boraginaceae): relationships with visitation by three bumblebee species and subsequent seed set

The fecundity of insect-pollinated plants may not be linearly related to the number of flowers produced, since floral display will influence pollinator foraging patterns. We may expect more visits to plants with more flowers, but do these large plants receive more or fewer visits per flower than small plants? Do all pollinator species respond in the same way? We would also expect foragers to move less between plants when the number of flowers per plant are large, which may reduce cross-pollination compared to plants with few flowers. We examine the relationships between numbers of inflorescence per plant, bumblebee foraging behaviour and seed set in comfrey, Symphytum officinale, a self-incompatible perennial herb. Bumblebee species differed in their response to the size of floral display. More individuals of Bombus pratorum and the nectar-robbing B.?terrestris were attracted to plants with larger floral displays, but B. pascuorum exhibited no increase in recruitment according to display size. Once attracted, all bee species visited more inflorescences per plant on plants with more inflorescences. Overall the visitation rate per inflorescence and seed set per flower was independent of the number of inflorescences per plant. Variation in seed set was not explained by the numbers of bumblebees attracted or by the number of inflorescences they visited for any bee species. However, the mean seed set per flower (1.18) was far below the maximum possible (4 per flower). We suggest that in this system seed set is not limited by pollination but by other factors, possibly nutritional resources.