The Structure of Pollen Wall and Its Relation to Po41en Aggregation in Cymbidium goeringii (Rchb. F.) Rchb. F.

The pollen wall of tetrads located in different positions of a mature pollinium of Cymbidium goeringii was examined with the electron microscope, and the compositions of wall materials were also tested with different histochemical methods. In all tetrads of a pollinium, the pollen wall can be distingished into an exine and an intine, but the exine may be varied greatly according to the tetrad position in a pollenium. The part of the pollen wall (the outer wall) of the external tetrads, lying close, to the tapetum, is composed of two layers, i.e. the exine, and the intine. Theexine consists of tectum, granulate ectexine and endexine, without foot layer. The intine is cellulose in nature. In the outer wall between different groups of: tetrads and in the inner wall within an individual tetrad, the structure of ectexine becomes simple and the deposition of sporopollenin is roduced The degree of reduction of ectexine nicreases from the outer to inner tetrads in several external layers of a pollinium, and even the internal tetrads have a reduced ectexine or lack of it. The present study also demonstrates that the mechanism of pollen aggregation into a pollinium is built on a combined effect of the following features: (1) connected bridges formed' by intine between two pollens within a tetrad, (2) formation of cytoplasmic channels between two pollens within a tetrad, (3) incomplete cell wall formation within a tetrad, (4) little size of tetrads and compact arrangement of mature tetrads and (5) a sticky viscin material surrounded on the outside of a pollinium.     

The pollinium ofLoroglossum hircinum (Orchidaceae) between pollination and pollen tube emission

The structure of the massulae composing the pollinium ofLoroglossum hircinum was studied before pollination and 12 and 24 hours afterwards. The grains are grouped in tetrads closely packed in massulae. The exine is only present on the outside of the massulae. The intine consists of two layers: a compact layer surrounding the pollen grain and a looser layer surrounding the pollen grain and a looser layer surrounding the tetrad. Twelve hours after pollination, pollen volume and the space between the tetrads increase due to vacuolization. Twenty-four hours after pollination, pollen volume and tetrad spacing are higher due to vacuolization and some grains have emitted pollen tubes. Pollen growth due to vacuole formation, and the absence of common walls between adjacent tetrads lead to crumbling of the massulae. The mature pollen grain does not have apertures: the site of pollen tube emission is determined after pollination. The first grains to germinate are those in the centre of the massula. The vegetative cell nucleus is the first to enter the pollen tube; the generative cell elongates and undergoes the second haploid mitosis shortly after entering the pollen tube.     

Pollen morphology and pollen-wall proteins (localization and enzymatic activity) inSesamothamnus lugardii (Pedaliaceae)

The pollen grains ofSesamothamnus lugardii Stapf (Pedaliaceae of subdesert regions of SE tropical Africa) are associated in acalymmate tetrads (cross wall cohesion), with a tectate and perforate exine and 8–12 colpi. The pollen wall consists of an ectexine with a complete, perforate and ample tectum, columellated infratectum and clearly interrupted and fragmented foot layer. The endexine is built of scanty lamellae and granules. The intine is bistratificate, with a homogeneous, fibrillate layer (endintine or intine-2) and a heterogeneous, more lax and channeled layer (exintine or intine-1). Test for glycoprotein is particularly positive in the homogeneous internal intine and channels of external intine. On the other hand acid phosphatase has been localized in the exine and channeled external intine layers. These observations confirm the general interpretation of the distribution of wall compounds.     

A New Pollen Type in the Winteraceae

Pollen of Zygogynum balansae and Z. pomiferum is described with the aid of the scanning electron microscope. Other members of the primitive ranalean family Winteraceae hitherto investigated have pollen in permanent tetrads, but these two species have solitary grains. Sculpturing is similar on the distal and proximal faces of each grain, excluding the distal apertural zone. The exine pattern resembles that on distal faces of tetrads of other Zygogynum species investigated, including Z. bailloni, the pollen of which is illustrated. Although Zygogynum and Exospermum have rather similar pollen, with sculpturing differing from other Winteraceae in consisting of a less coarse reticulum, pollen of Exospermum stipitatum is clearly distinct from the Zygogynum species investigated, as seen in the scanning electron microscope. It is not clear whether or not the solitary pollen type has evolved from the tetrad form.     

Studies on the Ontogeny of the Pollinium of Goodyera Procera

Using light, transmission and scanning electron microscopy, the development of the pollinium of Goodyera procera (Ker-Gawler) Hooker. was investigated. At the early stage, sporogenous cells inside the microsporangium were seen grouping together into small aggregates each containing few cells. After the aggregates have formed the sporogenous cells inside the aggregates (which could now be called massulae) divide to form numerous pollen mother cells. Later, the pollen mother cells undergo meiosis to form tetrads. The pattern of formation of the exine of tetrads varies according to the location of the tetrads inside the micro- sporangium. Those tetrads that are situated near the outer region of the massulae can form: exine with well developed tectum, bacula and foot layer; and the sequence of events leading to the formation of this type of well developed exine is as follows the original wall and the cyto- plasmic channels associated with the wall become surrounded by a thick layer of callose thus isolating the wall from the plasmalemma. Near the plasmalemma a layer of primexine containing callose and cellulose begins to form. Later, the primexine develops into exine and between the exine and plasmalemma a layer of intine is laid down. Similar type of exine with well developed tectum, bacula and foot layer, is also present in tetrads facing the tapetum. But in this case the original wall of the tedtrad is not retained but undergoes dissolution and in its place a new exine formed. The pattern of formation of exine in the region between tetrads is even more different. Here the original wall also undergoes dissolution but instead of forming a proper exine it only forms a thin foot layer with bulges at places. The pattern of formation of the exine in the cells inside the tetrad is even more different. Here the original wall of the cells only undergoes partial dissolution. The loose fibrils of the partially dissolved wall then become mixed with the callose layer surrounding the cell. Inside this wall-fibril/callose mixture thin sheets of exine appear, but these thin sheets of exine do not develop further into tectum or bacula. In Goodyera a quite substantial amount of callose is retained in the regions between massulae and tetrads, and we believe that it is this callose which is holding the massulae and tetrads together to form pollinium.     

Pollen wall development in Vigna vexillata I. Characterization of wall layers

Light and electron microscope observations characterized the layers that comprise Vigna vexillata L. pollen walls, and identified the timing of their development. Exine sculpturings form an unusually coarse ektexinous reticulum. The structure of the ektexine is granular; this differs from the columellate/tectate type of structure typical of most angiosperm pollen. The ektexine overlies a homogeneous-to-lamellar, electron-dense endexine, which in turn surrounds a thick, microfibrillar intine. Pollen grains are triporate and operculate, with Zwischenkörper and thickened intine underlying the apertures. The ektexine forms during the tetrad period of microspore development, the endexine and Zwischenkörper during the free microspore stage, and the intine during the bicelled (pollen) stage. Coarsely reticulate exine sculpturings and the granular structure of the patterned exine wall of the pollen grains are features that make this species suitable for detailed studies of pollen wall pattern formation.     

POLLEN WALL AND TAPETAL ORBICULAR WALL DEVELOPMENT IN SORGHUM BICOLOR (GRAMINEAE)

Pollen wall development in Sorghum bicolor is morphologically and temporally paralleled by the formation of a prominent orbicular wall on the inner tangential surface of the tapetum. In the late tetrad stage, a thin, nearly uniform primexine forms around each microspore (except at the pore site) beneath the intact callose; concurrently, small spherical bodies (pro-orbicules) appear between the undulate tapetal plasmalemma and the disappearing tapetal primary wall. Within the primexine, differentially staining loci appear, which only develop into young bacula as the callose disappears. Thus, microspore walls are devoid of a visible exine pattern when released from tetrads. Afterwards, sporopollenin accumulates simultaneously on the primexine and bacula, forming the exine, and on the pro-orbicules, forming orbicules. Channels develop in the tectum and nexine, and both layers thicken to complete the microspore exine. Channeled sporopollenin also accumulates on the orbicules. A prominent sporopollenin reticulum interconnects the individual orbicules to produce an orbicular wall; this wall persists even after the tapetal protoplasts degenerate and after anthesis. While the pollen grains become engorged with reserves, a thick intine, containing conspicuous cytoplasmic channels, forms beneath the exine. Fibrous material collects beneath the orbicular wall. The parallel development and morphological similarities between the tapetal and pollen walls are discussed.     

Development of the exineless pollen wall in Callitriche truncata (Callitrichaceae) and the evolution of underwater pollination

 The Callitrichaceae are a monogeneric family of aquatic angiosperms comprising approximately 50 terrestrial, amphibious, and obligately submersed species. Callitriche is unique in being the only known genus with co-occurring aerial and underwater pollination systems. Mature pollen structure is correlated with growth habit, pollination biology, and phylogeny within the genus. In the present study, development of exineless pollen in the obligately submersed species Callitriche truncata was examined, with particular emphasis on the tetrad stage. Pollen ontogeny occurred rapidly and non-synchronously; tetrads, free microspores, and two-celled pollen grains were identified within the same anthers. Formation of the intine also occurred relatively early, during the tetrad stage. Tetrads were surrounded by a structurally distinct envelope, and its ultrastructure and histochemistry indicate that this callose-like envelope is in a transitional state. Reduction or complete loss of the exine has evolved at least twice in Callitrichaceae, and the new ontogenetic data indicate that exine loss evolves more quickly than the loss of callose. In addition, developmental information on exineless pollen in C. truncata coupled with other palynological data for the exine-bearing terrestrial and amphibious growth forms provide support for the hypothesis that underwater pollination has had a relatively recent origin in the family. Received January 2, 2001 Accepted March 27, 2001     

Pollen morphology and ultrastructure of Australian Monimiaceae ‐ Austromatthaea,Hedycarya, Kibara,Leviera, Steganthera and Tetrasynandra

The pollen morphology and ultrastructure of Austromatthaea elegans, Hedycarya angustifolia, H. loxocarya, Kibara rigidifolia, Leviera acuminata, Steganthera macooraia and Tetrasynandra laxiflora, are described. All are Australian members of the Monimiaceae sensu stricto of the order Laurales, subclass Magnoliidae. Except for Hedycarya angustifolia, which has pollen grains in permanent tetrads, all species have small, globose, apolar, inaperturate pollen. They can be identified under SEM by their surface ornamentation: Austromatthaea has fossulate sculpturing; Hedycarya angustifolia has tetrads with a warty configuration; H. loxocarya has echinate pollen; Kibara has spherical gemmae with nipple‐like projections; Leviera has stellate sculpturing; Steganthera has a verrucose surface with small spherical projections on each verruca, and Tetrasynandra is gemmate with one to several spiny projections on each gemma. The pollen grains of all genera of Australian Monimiaceae sensu stricto, some the results of previous studies, are summarized in tabular form. The exine has no columellae, foot layer or endexine, in contrast to the family Atherospermataceae (syn. subfamily Atherospermatoideae of the Monimiaceae, sensu lato). The most elaborate type of wall structure consists of radial elements ("radial processes") with white line‐centered regions extending from beyond the intine to the tectal region and a two‐layered intine with an outer channelled part (onciform zone). Trends of evolution from this type are discussed and comparisons are made with other Monimiaceae, Lauraceae, Amborellaceae and Trimeniaceae.     

云南松花粉形态研究

在云南松(Pinus yunnanensis Fr.)小孢子发生发育过程中,花粉母细胞、四分孢子及花粉粒均见有粘连现象。花粉气囊的形态、大小变化复杂多样。除一般具两个正常气囊的花粉粒外,还观察到气囊不发育、具一个气囊、二个异形气囊、三个气囊和四个气囊的花粉粒。成熟花粉壁从外至内可分为外壁外层、外壁内层、内壁外层和内壁内层,它们的构成成分及形态均有明显差别。贮存后花粉的内壁结构发生了明显变化。     

Ultrastructure of microsporogenesis and microgametogenesis in Campsis radicans (L.) Seem. (Bignoniaceae)

In the present study, microsporogenesis, microgametogenesis and pollen wall ontogeny in Campsis radicans (L.) Seem. were studied from sporogenous cell stage to mature pollen using transmission electron microscopy. To observe the ultrastructural changes that occur in sporogenous cells, microspores and pollen through progressive developmental stages, anthers at different stages of development were fixed and embedded in Araldite. Microspore and pollen development in C. radicans follows the basic scheme in angiosperms. Microsporocytes secrete callose wall before meiotic division. Meiocytes undergo meiosis and simultaneous cytokinesis which result in the formation of tetrads mostly with a tetrahedral arrangement. After the development of free and vacuolated microspores, respectively, first mitotic division occurs and two-celled pollen grain is produced. Pollen grains are shed from the anther at two-celled stage. Pollen wall formation in C. radicans starts at tetrad stage by the formation of exine template called primexine. By the accumulation of electron dense material, produced by microspore, in the special places of the primexine, first of all protectum then columellae of exine elements are formed on the reticulate-patterned plasma membrane. After free microspore stage, exine development is completed by the addition of sporopollenin from tapetum. Formation of intine layer of pollen wall starts at the late vacuolated stage of pollen development and continue through the bicellular pollen stage.     

Pollen of Ceratostema (Ericaceae, Vaccinieae): tetrads without septa

The pollen morphology of two species of the Neotropical genus Ceratostema (Ericaceae) was examined by light, scanning and transmission electron microscopy. The Ceratostema species examined have 3-colporate pollen grains united in permanent tetrahedral tetrads that show a common condition encountered in the Ericaceae. But the septal exine was absent between two neighboring grains in each pollen tetrad of Ceratostema. The pollen tetrads without septa are the first report for the Ericaceae as well as other angiosperm families.     

Pollen structure, tetrad cohesion and pollen-connecting threads in Pseuduvaria (Annonaceae)

The structure of the pollen of 42 species of Pseuduvaria (Annonaceae) is described. The pollen is consistently inaperturate, isopolar and radially symmetrical. Four basic patterns of exine sculpturing are identified: rugulate, verrucate, scabrate and psilate. The exine stratification of one representative species, P. macrocarpa , is shown to be entirely ectexinal. The ectexine consists of a discontinuous outer tectal layer, a columellar infratectal layer, and an inner lamellar foliated foot layer; the intine is very thin and fibrillar. The pollen is invariably released as acalymmate tetrads, in which the tectum is absent from the proximal walls. The individual pollen grains within the tetrads are connected by crosswall cohesion, involving both exine and intine; this form of cohesion has not hitherto been reported in the Annonaceae. In addition, pollen grains of neighbouring tetrads are connected in two different ways, viz. short exine connections and non-sporopollenin pollen-connecting threads. Neither of these cohesion mechanisms has previously been reported for the genus. The function of the various forms of cohesion between pollen grains and tetrads in Pseuduvaria is discussed as a mechanism to enhance the efficiency of pollination by enabling the fertilization of multiple ovules following a single pollinator visit.  © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society , 2003, 143 , 69−78.     

THE POLLEN WALL OF CANNA AND ITS SIMILARITY TO THE GERMINAL APERTURES OF OTHER POLLEN

The pollen wall of Canna generalis Bailey is exceptionally thick, but only a minor part of it contains detectable amounts of sporopollenin. The sporopollenin is in isolated spinules at the exine surface and in the intine near the plasma membrane. There is no sporopollenin in the > 10 μ thick channeled region between spinules and intine. We suggest that the entire pollen wall of C. generalis is similar to the thick intine and thin exine typical for germinal apertures in many pollen grain types. Considered functionally, the Canna pollen wall may offer an infinite number of sites for pollen tube initiation and would differ significantly from grains that are inaperturate in the sense of an exine lacking definite germinal apertures.     

Beschorneria yuccoides and Asimina triloba (L.) Dun: Examples for proximal polar germinating pollen in angiosperms

Beschorneria yuccoides (Agavaceae) microspores are arranged mostly in planar tetrads. Later on, the pollen grains of the tetrad usually fall apart, but sometimes remain loosely connected by ektexine elements. The ektexine consists of a tectum, of short columellae, and of a thin, discontinuous foot layer. An endexine is absent. The bilayered intine is without any additional thickening that would usually indicate an aperture region. From this point of view the pollen grain might be considered as omniaperturate. The pollen ornamentation is reticulate with wide lumina and robust, smooth muri.

The pollen grains show an indistinct sulcus characterised by a loose reticulate ornamentation. The sulcus is not exactly at the distal pole, but shifted towards the equator. No pollen tubes are formed regularly at the sulcus. Instead, pollen tubes are normally formed at the proximal pollen face. The proximal area, indicating a large germination field, is morphologically and functionally clearly an aperture (a germination zone); however, it does not represent a sulcus. The proximal face of all pollen grains appears as ornamented, with some exine lumps.

Asimina triloba (Annonaceae) pollen is shed in permanent planar or decussate tetrads. The distal sides are microreticulate to foveolate, and do not show an aperture; the psilate proximal sides are the germination areas of A. triloba.

The presence of apertures placed at the proximal pole was reported for distinct taxa of several angiosperm families. For Drosera, Dionaea (Droseraceae) and most probably for the diaperturate Cuphea species (Lythraceae) the existence of polar germination areas can be excluded. However, in some Annonaceae taxa with permanent tetrads (Annona cherimola, Asimina triloba) a situation similar to Beschorneria might be present, and indeed a proximal polar pollen tube is formed. Beschorneria yuccoides, Annona cherimola and Asimina triloba are unequivocal examples of angiosperm pollen with an exactly proximal aperture (germination area).     

ULTRASTRUCTURE AND DEVELOPMENT OF THE NEXINE AND INTINE IN THE POLLEN WALL OF SILENE ALBA (CARYOPHYLLACEAE)

Nexine and intine development in Silene alba (Caryophyllaceae) was investigated by electron microscopy and enzyme cytochemistry. Nexine-2 forms by deposition of sporopollenin along unit membrane lamellae closely associated with the microspore plasma membrane in the late tetrad stage. After the callose wall dissolves, electron density increases along the tangentially oriented fibers of the proximal primexine, forming nexine-1. When the exine is essentially complete, the intine begins to develop. In the nearly mature microspore, acid phosphatase activity appears in the peripheral cytoplasm just prior to its extrusion into the intine of the mature pollen grain.     

Microsporogenesis and microgametogenesis of the Argentinian species of Podocarpus (Podocarpaceae)

The development of the microsporangium and male gametophyte of three species of Podocarpus was studied with light microscopy (LM) and the morphology of pollen with scanning and transmission electron microscopy (SEM and TEM). During early stages, the male cone is covered with coriaceous scales. The archesporid cells go through a dormant period. Later the pollen mother cells differentiate and undergo meiosis. Callose is detected around the tetrad and between each monad. The microspore nucleus divides several times to give rise to a multicellular gametophyte, which includes the tube cell, the stalk and body cells, and four prothallial cells. The exine of the pollen grain is rugulate in the corpus and quite smooth in the sacci. The ultrastructure of the pollen wall consists of the alveolate sexine, the laminate nexine I and the amorphous nexine II. The intine is very thin. Comparison of the mature grain of some fossils with living members of the Podocarpaceae reveals great similarity.     

含笑花药发育的超微结构研究

对含笑花药发育中的超微结构变化进行观察,结果显示:(1)花粉发育中有三次液泡变化过程——第一次是小孢子母细胞在形成时内部出现了液泡,这可能与胼胝质壁的形成有关;第二次是在小孢子母细胞减数分裂之前,细胞内壁纤维素降解区域形成液泡,它的功能可能是消化原有的纤维素细胞壁;第三次是在小孢子液泡化时期,形成的大液泡将细胞核挤到边缘,产生极性。(2)含笑花粉在小孢子早期形成花粉外壁外层,花粉外壁内层在小孢子晚期形成,而花粉内壁是在二胞花粉早期形成;花粉成熟时,表面上沉积了绒毡层细胞的降解物而形成了花粉覆盖物。研究认为,含笑花粉原外壁的形成可能与母细胞胼胝质壁有关,而由绒毡层细胞提供的孢粉素物质按一定结构建成了花粉覆盖物。     

Polarity, aperture condition and germination in pollen grains ofEphedra (Gnetales)

Pollen grain polarity, aperture condition and pollen tube formation were examined inEphedra americana, E. foliata, E. rupestris, E. distachya, andE. fragilis using LM, SEM and TEM. In the characteristic oblate pollen, as seen in situ in the tetrad configuration, the polar axis is the minor one and the equatorial plane runs between the two narrow ends of the microspore. The intine is thick in fresh fixed mature pollen but we have seen no indication of regions having an exceptionally thick intine that could be considered associated with an aperture or apertures. About three minutes after transferring fresh pollen to the germinating medium the ridged exine splits and twists away from the intine and its enclosed protoplast. The shed exine spreads out and curls into a scroll-like configuration that is as distinctive as that of the pollen shape had been but now having the ridges and valleys perpendicular to the long axis. The pollen tube develops, in our experience with more than a hundred germinating pollen grains, near one of the narrow tips of the pollen grain's equatorial plane. The location of the pollen tube initiation probably is related to the position of the tube cell nucleus. The pollen tube starts to grow about one hour after the exine was shed. The pollen tube emerges close to the narrow end (equator) of the gametophyte. This end emerged first as the exine is shed and is opposite to the prothallial cells. The stout pollen tube is c. 10µm in diameter grown in vitro on agar. In our germination medium the stout tube continued to elongate for about 24 hours reaching a length of c. 100 µm. With respect to exine morphology the aperture condition could be considered as inaperturate. The pollen tube, however, is formed in a germination area near one end of the exineless gametophyte.