Sporoderm and tapetum development in Eupomatia laurina (Eupomatiaceae). An interpretation

For the first time, the developmental events in the course of exine structure establishment have been traced in detail with TEM in Eupomatia, with the addition of cytochemical tests. A new look at unfolding events is suggested using our recent hypothesis on self-assembling micellar mesophases. The process proved to be unusual and includes “ghost” stages. The first units observed in the periplasmic space are spherical ones (= normal spherical micelles). These accumulate, resulting in a granular layer up to middle tetrad stage. Sporopollenin precursor accumulation on these units makes the ectexine layer looking as homogenous at late tetrad stage. Simultaneously, the columns of globules are added in the periplasmic space, which reminds an attempt to form columellae; but, the process failed. Instead, a fimbrillate endexine layer of compressed globules appears. The latter augments via additional globules, appearing in the periplasmic space in the free microspore period. The endexine formation is double-stepped spatially and temporally. The second, lamellate endexine layer (laminate micelles) appears late in development, when the channeled intine-I is already established—a very unusual feature. Moreover, a “fenestrated” stage comes unexpectedly at vacuolate stage, when hitherto amorphous ectexine appears pierced by cavernae—the results of reversal of normal spherical micelles (constituents of ectexine) to reverse the ones that open their cores for the entrance of hydrophilic nutrients from tapetum and give them over to the microspore cytoplasm by exchanging their solubilizates.     

Exine and tapetum development in Nymphaea capensis (Nymphaeaceae): a comparative study

The developmental events in microspore envelope and cytoplasm and in tapetum from premeiosis until late tetrad stage were studied in Nymphaea capensis. The exceptional feature of microspore development in this species is that post-meiosis cytokinesis is retarded until the late tetrad stage. Thus, the entire development of the exine becomes completed during the tetrad stage. As a consequence of the retarded cytokinesis, the proximal portion of the forming exine lags behind the distal one during the major part of the tetrad period, but eventually the proximal part of the exine overtakes the distal part in development. The significance of this retardation is discussed. This sequence of events differs sharply from corresponding sporoderm development in other Nymphaea species. Another important topic is the microspore surface activities during exine development. The surface coatings-glycocalyx-are very similar in microspores and in tapetum cells, but their functions are completely different; the roots for this difference are discussed. A noteworthy feature of the developing microspores is the presence of gigantic, deeply cup-like mitochondria; this property is also characteristic of the microspore cytoplasm of N colorata and N. mexicana. A functional significance of these organelles and their adaptive role is discussed.     

Chemotaxonomy of theSymphytum officinale agg. (Boraginaceae)

In a chemotaxonomic study of the genusSymphytum pyrrolizidine alkaloids and triterpenes were used as chemotaxonomical markers. A micro-extraction methods was developed for screening compounds of very small pieces of herbarium material. The occurrence of the pyrrolizidine alkaloids symphytine and (acetyl-)lycopsamine is very general forSymphytum taxa. Echimidine is present in someS. officinale L. plants and inS. tanaicense Steven. The triterpene isobauerenol is present inS. officinale, S. bohemicum Schmidt,S. tanaicense and inS. officinale var.lanceolatum Weinm. The chemotaxonomic hypothesis, proposed byGadella and collaborators, based on the presence of the triterpene isobauerenol inS. officinale and its absence inS. asperum Lepech. and the presence of the pyrrolizidine alkaloid echimidine inS. asperum and its absence inS. officinale, can no longer be applied absolutely to theS. officinale species complex. The pyrrolizidine alkaloid and triterpene pattern ofS. officinale (2n = 24) andS. bohemicum (2n = 24) is identical.S. bohemicum is morphologically, cytologically and phytochemically very similar toS. officinale. Furthermore, it readily crosses with the white flowered W. European diploids ofS. officinale. Therefore it seems likely that these two taxa are conspecific.S. tanaicense shows a pyrrolizidine alkaloid and triterpene pattern similar toS. officinale (2n = 40). Also on morphological and cytological grounds they are very similar. It seems highly probable thatS. tanaicense is conspecific withS. officinale (2n = 40) and represents an intraspecific variant only.S. officinale var.lanceolatum contained no pyrrolizidine alkaloids but did contain isobauerenol. This feature points to an origin fromS. officinale.     

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.     

中国紫草科破布木属花粉形态和外壁超微结构

为了深入探讨紫草科（Boraginaceae）的分类问题,用光学显微镜和扫描电子显微镜观察了该科破布木属（CordiaL.) 10种植物的花粉形态和外壁超微结构。发现该属花粉具三孔、三孔沟、三拟孔沟和三合沟4种萌发孔类型。外壁表面具微刺状纹饰、刺状纹饰、网状纹饰和不规则的条纹网状纹状。破布木属的花粉特征表明,该属花粉在紫草科中既是独特的分类群,又是比较原始的属种。     

Population substructure in Alkanna orientalis (Boraginaceae) in the Sinai Desert, in relation to its pollinator behaviour

Subpopulation genetic structure was studied in a population of the short-lived perennial plant Alkanna orientalis from the Sinai Desert, Egypt. The population investigated was subdivided for sampling into four subpopulations, which were located within three steep-sided wadis and a central plain area. Results from previous studies suggested that bee pollinator behaviour was likely to cause limited gene dispersal within the population and that subpopulations might have diverged from each other genetically. Seven RAPD primers were used to detect polymorphisms in the population. Differences between sub-populations in fragment frequency were found for several of the 45 polymorphic RAPD fragments scored. Population subdivision was evident from cluster analysis, and an analysis of genetic distances showed that there was significant genetic differentiation between all subpopulations. Nevertheless, more extensive gene flow appears to take place within the population than was expected, as demonstrated by a higher level of genetic similarity between subpopulations from two of the narrow wadis and the interconnecting plain. It is suggested that seed transport mediated by periodic flash floods is responsible for this pattern.     

Exine development in Nymphaea colorata (Nymphaeaceae)

We show a sequence of developmental events in microspores and tapetal cells in Nymphaea colorata based upon transmission and scanning electron microscopic observations. There are parallel cytoplasmic processes and surface coatings in microspores and tapetal cells. Uptake is indicated by the passage of lanthanum as a tracer from anther locule into the microspore cytoplasm and by the condition of the cytoplasmic surface of microspores. The callose envelope is not a barrier to transfer of lanthanum. During formation of the proexine glycocalyx tiny spiral elements, components of the exine substructural units, were oriented in different directions in the surface coating of microspores and tapetum. Lipoidal globules are associated with the spiral elements. After the uniform proexine stage, three regions of different exine structure and their gradations become differentiated in the sporoderm: 1) a proximal region with thick tectum and foot layer, thin columellae and a compact layer of lamellated endexine; 2) a distal pole region with separately disposed endexine lamellae; and 3) an equatorial encircling-sulcate aperture region which consists of infratectal layer, foot layer, and endexine lamellae. Based upon the presence of structurally comparable surface coats in microspores and tapetal cells, experimental uptake of lanthanum nitrate, and the co-ordinated processes in tapetum and microspores, we conclude that there is probably a reciprocal controlling influence between the microspores and the tapetum and other sporophytic tissues.     

Plasmodial tapetum and pollen wall development in Butomus umbellatus (Butomaceae)

This report describes the ultrastructural development of plasmodial tapetum and pollen wall of Butomus umbellatus. The tapetum contains extensive arrays of rough endoplasmic reticulum, vesicles from which are responsible for the formation of sporopollenin-like bodies. The tapetum is also involved in the formation of other forms of sporopollenin precursors. Development of pollen wall continues after microspores are released from their callosic walls; they are then enclosed by plasmodial tapetum. The activity and products of the plasmodial tapetum show substantial correlation with pollen wall development, particularly ektexine formation. In B. umbellatus, the tapetum intrudes into the anther locule at early microspore stage. This timing of plasmodial intrusion occurs at a later stage of pollen development as compared to those in the advanced monocotyledons. We report the rough endoplasmic reticulum origin of sporopollenin-like bodies and their occurrence in the plasmodial tapeta of B. umbellatus.     

Chemotaxonomical investigations of theSymphytum officinale polyploid complex andS. asperum (Boraginaceae): Phytosterols and triterpenoids

From a comparison of phytosterol and triterpenoid patterns of severalSymphytum officinale cytotypes,S. asperum and their interspecific hybrids,S. ×uplandicum, which were obtained from thin layer chromatography and gaschromatography (also in combination with mass spectrometry), the hybrid character of the latter taxon is clearly shown. The specific value of the triterpenoid isobauerenol as a chemotaxonomical marker within this group is discussed in some detail.     

Pollen, tapetum and orbicule development in Modiolastrum malvifolium (Malvaceae)

Background and Aims: Although orbicular functions are still a matter of debate, theyare considered by most authors to be exclusively formed by asecretory tapetum. However, the presence of orbicules on a peritapetalmembrane associated with a plasmodial tapetum has been describedfor Abutilon pictum (Malvaceae) in a previous study. Thus, studieson other species of Malvaceae are necessary to corroborate thepresence of such bodies in other members of the family. Pollenand microsporangium development of Modiolastrum malvifoliumhas been studied in this work. Methods: Anthers at different stages of development were processed fortransmission electron microscopy and light microscopy. Membranesand pollen walls resistant to acetolysis were isolated fromwhole anthers. Key Results: Microspore tetrads have a tetrahedral arrangement. Pollen grainsare shed at the bicellular stage. The tapetum is invasive, non-syncytialand a peritapetal membrane with orbicules is formed. Conclusions: This is the first report of the presence of orbicules on a peritapetalmembrane in a species with a tapetum of an invasive, non-syncytialtype. Taking into consideration all the information on the subject,it can be concluded that the presence of orbicules is not astable criterion to differentiate between a secretory or plasmodial,or intermediate invasive, non-syncytial tapetum.     

Chemotaxonomical investigations of theSymphytum officinale polyploid complex andS. asperum (Boraginaceae): The pyrrolizidine alkaloids

By means of thin layer chromatography in conjunction with mass spectrometry the pyrrolizidine alkaloid patterns derived fromSymphytum asperum, several cytotypes ofS. officinale agg. and the artificial hybrids of the former taxa, were compared. The obtained patterns were not essentially affected by variation in cytotype, harvesting times and -location of plants. Lycopsamine, acetyl-lycopsamine and symphytine or their isomers were generally found in theS. officinale cytotypes, echimidine and symphytine inS. asperum. The interspecific hybrids contained all alkaloids mentioned. The definite lack of echimidine in the 2 n=40 cytotype proves that it is conspecific withS. officinale and does not belong to a hybrid-swarmS. asperum × S. officinale with 2 n=48. Part I of this series of contributions.     

The rice tapetum degeneration retardation gene is required for tapetum degradation and anther development

In flowering plants, tapetum degeneration is proposed to be triggered by a programmed cell death (PCD) process during late stages of pollen development; the PCD is thought to provide cellular contents supporting pollen wall formation and to allow the subsequent pollen release. However, the molecular basis regulating tapetum PCD in plants remains poorly understood. We report the isolation and characterization of a rice (Oryza sativa) male sterile mutant tapetum degeneration retardation (tdr), which exhibits degeneration retardation of the tapetum and middle layer as well as collapse of microspores. The TDR gene is preferentially expressed in the tapetum and encodes a putative basic helix-loop-helix protein, which is likely localized to the nucleus. More importantly, two genes, Os CP1 and Os c6, encoding a Cys protease and a protease inhibitor, respectively, were shown to be the likely direct targets of TDR through chromatin immunoprecipitation analyses and the electrophoretic mobility shift assay. These results indicate that TDR is a key component of the molecular network regulating rice tapetum development and degeneration.     

Comparative floral development in Lithospermum (Boraginaceae) and implications for the evolution and development of heterostyly

? Premise of the study: The evolution and development of floral developmental patterns were investigated in three heterostylous and three homostylous species of Lithospermum to determine whether species that independently acquired the same floral form follow the same pattern of development or different patterns. ? Methods: Using light and scanning electron microscopy, we observed developmental patterns in flowers at different stages of maturity. These patterns were compared within individual species, between heterostylous morphs, and among heterostylous and homostylous species. ? Key results: Although heterostyly has been determined by phylogenetic analysis to have originated independently in each of the heterostylous species, flowers of the long-style morph of each species follow similar patterns of gross development, as do those of the short-style morph. In addition, the flowers of each morph develop in a manner similar to those of their respective homostylous, herkogamous relatives. However, the developmental patterns of the stylar epidermal cells differ among these species and between heterostylous and homostylous species. ? Conclusions: Floral developmental patterns in homostylous species provide evidence that modification of specific traits, such as patterns of stylar growth, can lead to the evolution of heterostyly. The developmental changes that affect the positions of the stigmas and anthers in each morph likely involve either temporal or spatial modifications of gene function. The floral developmental patterns described here and the occurrence of multiple types of herkogamy within some species of Lithospermum provide evidence that heterostylous species in the genus have originated via distinct evolutionary developmental pathways.     

Exine Sculpture in Pariana Pollen (Gramineae)

Pollen grains of eieven species of Pariana, a small genus of herbaceous bamboos, were studied using LM, SEM and TEM. Ten of them have the Pariana stenolemma-type of pollen characterized by areolate exine due to relatively high and well separated denticulate processes on a slightly undulated tectum, vestigial columellae and no distinct annulus. At the pore edge the foot layer is thickened and folded.

P. campetris (P. campestris-type) shows this exine feature only at magnifications higher than x 2000, whereas the denticulate processes are clearly visible at x 400 magnification in the other ten species. The pores are bordered by a distinct annulus.

The high relief of the Pariana pollen forming a relatively rough surface would offer more friction in wind transport than the smooth surface of other grass pollen grains. Insects visiting the flowers have been observed which support the idea of possible insect pollination. If this would be the case, the parianas would be an example of correlation between pollen form and function in the evolution of the Gramineae.     

Direct and indirect estimates of the selfing rate in small and large individuals of the bumblebee pollinated Cynoglossum officinale L (Boraginaceae)

We measured the relationship between selfing rates and flower number in an experimental population of bumblebee pollinated Cynoglossum officinale , with plants differing in flower number. Results were compared with the prediction of a model based on pollen dynamics and pollinator behaviour. The selfing rate, as measured by multilocus oligonucleotide DNA fingerprinting, increased with flower number and ranged from 0% to 70%. Flowers on large plants received an equal number of visits from bumblebees as flowers on small plants. On large plants more flowers in a row were visited, inducing geitonogamy. The overall relationship between selfing rate and number of flowers can be explained by pollen dynamics and pollinator behaviour without invoking postpollination processes such as differential pollen tube growth and abortion.     

The tapetum inSchizaea pectinata (Schizaeaceae) and a comparison with the tapetum inPsilotum nudum (Psilotaceae)

A combination tapetum consisting of a cellular, parietal component and a plasmodial component occurs inSchizaea pectinata. A single, tapetal initial layer divides to form an outer parietal layer which maintains its cellular integrity until late in spore wall development. The inner tapetal layer differentiates into a plasmodium which disappears after the outer exospore has developed. In the final stages of spore wall development, granular material occurs in large masses and is dispersed as small granules throughout the sporangial loculus. No tapetal membrane develops. Comparisons are drawn with the combination tapetum found inPsilotum nudum.     

Anatomy and evolution in MacaronesianEchium (Boraginaceae)

The endemic Macaronesian members of the genusEchium (Boraginaceae) were examined anatomically to elucidate their relationships. Vessel length to breadth ratio was used as the initial guide to the relative primitive or derived nature of each taxon. Together with other features (e.g. trichome structure) it was possible to establish the phylogenetic pathways within this recently evolved relict group (Fig. 1).