Re-Exposure of Tapes at High Temperature and Pressure in the Lycopodium Clavatum Spore Exine

Lamellations are visualizable through the staining commonly used in transmission electron microscopy during exine formation on Lycopodium and other spores, and the nexine of pollen grains. The lamellations so exposed consist-of dark tapes at either side of an unstained (white) line. Neither tapes nor white lines are visualizable in the exine of mature spores of Lycopodium. The continued presence of lamellations having tape-white line spacing has been demonstrated with inorganic tracers in the nexine of pollen in which lamellations otherwise appeared to be absent. Through high contrast staining methods for TEM we have observed lamellations in the residual exine following heat treatment (350[ddot]C) of mature spores of Lycopodium clavatum. The surface of these residual exines was etched by treatment with hot 2-aminoethanol and filaments were observed to protrude from the etched surfaces. The residual exine stained darkly. Lycopodium spores heated to 300[ddot]C at 1 kb pressure had long filaments exposed at the surface of the residual exine (sporopollenin). Sections of the pellet remaining after heat and pressure treatment also included bundles of closely parallel filaments and masses of isolated filaments. The filaments were stained while the exine residue, assumed to include sporopollenin, was not. Isolated filaments produce a stable metachromasia with toluidine blue indicating the presence of many closely spaced sites of negative charge. The staining of intact exines with basic dyes may result from anionic sites on filaments embedded within the exine rather than being due to sporopollenin. The results of our experiments indicate that the filaments are more resistant to heat and pressure and 2-aminoethanol than is sporopollenin. We propose that the trilamellar elements commonly called tapes and white lines might be composed of two filaments bridged by polybasic molecules.     

Exine ultrastructure of in situ peltasperm pollen from the Rhaetian of Germany and its implications

Morphology and exine ultrastructure of pollen grains of Triassic peltasperms have been studied for the first time. Pollen grains of Antevsia zeilleri from the Rhaetian of Germany are of the Cycadopites-type and monosulcate; the sculpturing is the same in the apertural and non-apertural areas. The proximal exine includes a row of lacunae covered by a solid, thick tectum and underlined by a foot layer. Pillars are hanging from the tectum between the lacunae. The exine is thinning to a homogeneous layer in the apertural region. The latter is bordered by thicker alveolate areas of the exine, in places resembling a saccus-like ultrastructure. The endexine includes white-line-centred lamellae. The exine ultrastructure is compared with that of pollen of Permian peltasperms. Although pollen types ascribed to Permian peltasperms are completely different in their general morphology, a transformation can be hypothesized by ultrastructural data from Permian Vesicaspora into Triassic Cycadopites extracted from pollen sacs of Antevsia. Comparison with Cycadopites of non-peltaspermalean (Ginkgoalean, Cycadophyte) and unknown affinities has been accomplished. The exine ultrastructure is distinctive enough to differentiate among peltaspermalean, cycadalean and bennettitalean Cycadopites; some ultrastructural features are shared with pollen of modern Ginkgo biloba. More ultrastructural data are needed as well as numerous sections of pollen grains are necessary to reveal original unchanged ultrastructure.     

Microspore and tapetal development in Echinodorus cordifolìus (Alismaceae)

In the microspore tetrad period the exine begins as rods that originate from the plasma membrane. These rods are exine units that on further development become columellae as well as part of the tectum, foot layer and “transitory endexine”. The primexine matrix is very thin in the future sites of the pores. At these sites the plasma membrane and its surface coating (glycocalyx) are without exine units and adjacent to the callose envelope. The exine around the aperture margin is characterized by units of reduced height. After the exine units and primexine matrix have become ca 0.2 μm in height a fibrillar zone forms under the aperture margin. It is the exine units around the aperture that are templates for exine processes on apertures of mature pollen. Oblique sections of the early exine show that the tectum consists of the distal portions of close-packed exine units. The exine enlarges in the free microspore period but initially its substructure (tectum, columellae, foot layer and transitory endexine) is not homogeneous and unit structures are visible until after the vacuolate microspore period. There are indications of a commissural line/plane (junction plane) which separates the foot layer from the endexine during early development. Our observations of development in Echinodorus pollen extend a growing number of reports of “transitory endexines” in monocot pollen. The exine unit-structures become 0.2 μm or more in diameter and many columellae are composed of only one exine unit. Spinules become exceptionally tall, many protruding ca 0.7 μm above the level of the tectum as units only ca 0.1 μm in diameter. The outer portion of the tectum fills in around spinules and by maturity they are microechinate with their bases spread out to ca 1 μm or more. Unit structures can be seen with SEM in mature pollen following oxidation by plasma ashing and in the tapetum these units are arranged both radially, as in spinules, and parallel with the tapetal surfaces. There are clear indications of such an arrangement of units in untreated fresh pollen. Units comprising the basal part of the exine are not completely fused by sporopollenin accumulated during development. This would seem to be a characteristic feature, based on published work, of the alismacean pollen. Our use of a tracer shows, however, that there is considerable space within or between exine structure of mature Echinodorus pollen. Based upon the ca 0.1 μm size of exine-units formed early in development and exine components seen after oxidative treatment it seems that the early (primary) accumulated sporopollenin has greater resistance to oxidation than sporopollenin added, secondarily, around and between units later in development. Both primarily and secondarily accumulated sporopollenin are resistant to acetolysis but published work indicates that acetolysis alters exine material. At the microspore tetrad time and until the vacuolate stages tapetal cells are arranged as in secretory tapetums. During early microspore stages there are orbicules at the inner surface of tapetal cells. At free microspore period tapetal cells greatly elongate into the loculus and surround the microspores. By the end of the microspore vacuolate period tapetal cells release their cellular contents and microspores are for a time enveloped by tapetal organelles and translocation material.     

Dynamic of polysaccharide and lipid in the developing microsporangiums of Chinese fir (Cunninghamia lanceolata)

Microsporongium development in Chinese fir (Cunninghamia lanceolata) was investigated using cytochemical methods with a special attention to the fluctuations (in amount and distribution) of polysaccharide and lipid reserves along the development of the microsporangium. Semi-thin sections of microsporangia at different developmental stages were stained with periodic acid–Schiff (PAS) reagent and Sudan Black B to detect insoluble polysaccharides and neutral lipids, respectively. In young microsporangia, microspore mother cells began to accumulate starch grains and lipids, which disappeared during microspore development. Following microspore division, the starch grains present in bicellular pollen disappeared and abundant lipid deposits were accumulated. In mature pollen, only abundant lipids accumulated as storage material. The pollen wall of C. lanceolata is predominantly composed of polysaccharidic intine, and the sporopollenin-containing exine is weakly developed and only forms a thin layer covering the intine.     

The ultrastructure of fossil dispersed monosulcate pollen from the Early Cretaceous of Transbaikalia,Russia

The general morphology, surface sculpturing, and exine ultrastructure have been studied in dispersed monosulcate pollen from the Early Cretaceous of Transbaikalia, Russia. The pollen grains dominate the palynological assemblage extracted from coal deposits of the Khilok Formation in the Buryat Republic, which also contain ginkgoalean leaves of Baierella averianovii as the only constituent of the assemblage of plant megafossils. The relationship between the pollen grains and ginkgoalean leaves from this autochthonous burial is hypothesised on the basis of taphonomical analysis and palaeobiogeographical data. It is shown that the ectexine of the pollen grains includes a thick solid tectum, a thin granular infratectum and a thin foot layer; the endexine is fine-grained, slightly more electron-dense than the ectexine, and is preserved only in places. The distal aperture is formed by a thinning of the exine. No analogous ultrastructure has been described so far in fossil pollen grains of this morphotype studied ultrastructurally from in situ material. For comparison, we also studied the exine ultrastructure of pollen grains Ginkgo biloba. The fossil pollen is not identical to pollen of extant G. biloba, but shows several significant similarities in the exine ultrastructure, which does not contradict the presumable ginkgoalean affinity of the fossil pollen.     

A unique pollen wall mutation in the family Compositae: ultrastructure and genetics

During a routine screening of pollen fertility in the n = 2 chromosome race of Haplopappus gracilis, a spineless pollen wall mutation was discovered that renders the otherwise functional pollen grains completely unrecognizable as Compositae pollen. Normal Haplopappus pollen is characterized by an outer layer, the ektexine, consisting of large spines supported by a roof (tectum), which in turn is supported by collumellae that are joined basally. A large cavity (cavea) stretches from aperture to aperture and separates columellae bases from the final ektexine unit, the foot layer. The spines, tectum, columellae, and columellae bases are filled with perforations (internal foramina), while the foot layer is without them. Immediately underlying the foot layer is a thickened, lamellate, disrupted, internal foramina-free second exine layer, the endexine. In contrast, the mutant pollen ektexine is a jumble of components with randomly dispersed spines as the only clearly definable unit. The endexine layer is similar to the endexine in normal pollen. The mutation apparently disrupts only the organization of ektexine units, and mutant pollen appears to be without the caveae and foot layer characteristic of normal pollen. In genetic tests, the mutant allele is recessive. There is a simple Mendelian pattern of inheritance of the mutant gene, and its phenotype is under sporophytic control.     

Pollen morphology of the genera Polygonum s. str. and Polygonella (Polygoneae: Polygonaceae)

The pollen of 30 taxa (27 species, one subspecies and two varieties) in two genera, viz Polygonum s. str. and Polygonella was investigated with LM and SEM, and some selected taxa with TEM. In all genera investigated the pollen is prolate to spheroidal, and the aperture is mostly tricolporate, rarely panto-hexacolporate (especially Polygonum section Polygonum). The exine sculpturing pattern is the most variable feature. Three types of exine can be recognized. Type 1 (Avicularia-Type, sensu Hedberg) - All species of section Polygonum and section Tephis share the smooth tectate exine with spinules, sometimes the surface is more or less rough (Polygonum afromontanum in section Tephis). Type 2 (Pseudomollia-Type, sensu Hong) - Pollen of Polygonum molliaeforme (section Pseudomollia) has the exine, which is verrucose on both poles and nearby the mesocolpium, and mostly psilate around the ectoaperture. Type 3 (Duravia-Type, sensu Hedberg) - Pollen grains of Polygonum section Duravia and Polygonella have the exine which is semitectate-reticulate at the mesocolpium and the poles, and rugulate/reticulate or sometimes foveolate with microspinules around the ectoapertures. The pollen grains in four taxa (viz Polygonum section Pseudomollia, P. section Duravia and genus Polygonella) have a well-marked dimorphism of the ektexine, which is considered to be a synapomorphic condition. The differences of pollen grain between the genus Polygonella and Polygonum section Duravia are almost non existent and clearly interrelated. It is therefore postulated that the similarity in pollen of both taxa is not the result of convergency, but is interpreted as a homology. It is noteworthy that the pollen of Polygonum molliaeforme (section Pseudomollia) appears as intermediate between the Avicularia-type and the Duravia-type, and is well supported the value of separated section for its own. Additionally, in TEM, some exine ultrastructures (e.g. columellae, foot layer, endexine) appear to be valuable characters for comparison between/among taxa. The systematic potentialities of the pollen data of the studied taxa at various systematic levels are also discussed.     

Cytochemistry of pollen development in Brachypodium distachyon

Brachypodium distachyon is a widely recognized model plant belonging to subfamily Pooideae with a sequenced genome. To gain a better understanding of the male reproductive development in B. distachyon we examined pollen morphology and cytochemical changes of microspore cytoplasm from pollen mother cell stage to mature pollen using light, fluorescent and scanning electron microscopy. Our results show that B. distachyon exhibits a typical monocot-type pollen ontogeny. Meiosis in the pollen mother cells is accomplished by successive cytokinesis generating isobilateral tetrads. Cytochemical examination indicated that microspore cytoplasm contains variable amounts of insoluble carbohydrates and proteins at different developmental stages. Deposition of starch in the cytoplasm of microspores starts at the bicellular stage and continues till the mature pollen stage. The formation of the exine wall progresses by the deposition of sporopollenin from the tapetum layer of the anther. The mature pollen is trinucleate, spheroidal in shape and possesses a single pore with an annulus and operculum. The exine pattern is smooth and of granular type.     

Developmental stages of the pollen wall and tapetum in some Crocus species

The developmental stages of the pollen wall and tapetum, together with exine morphology were studied in a number of Crocus species, by light and scanning electron microscopy. Gametogenesis was characterized by: 1) development of a thick intine, 2) single mitosis, and 3) terminal amylolysis. The tapetum was of the secretory type. In C. cartwrightianus cv. albus, abnormal sporogenesis and gametogenesis produced vacuolate pollen grains with a reduced-or no intine layer, and rich with starch granules; the tapetum was either of the parietal-or amoeboid type. The exine was echinate and the pollen grains had different types of aperture: furrows, colpi or pores. The ornamentation varied from microreticulate to irregularly perforate. The exine framework was overlaid by a pellicle resistant to chloroform-carbon disulphide, on which a layer of pollenkitt was deposited. The results are discussed from both cytological and evolutionary viewpoints.     

The fine structure of the pollen wall inStrelitzia reginae (Musaceae)

The pollen wall ofStrelitzia reginae (Musaceae) consists of a nearly unsculptured, very thin, highly reduced, but coherent exine, and a thick intine (with an outer, channeled layer and an inner, largely homogeneous layer). After short, incomplete acetolysis the exine covers the remaining, severely shrinked protoplast as a folded, but unaltered “skin”, while the intine has totally disappeared. After extended acetolysis only the coherent, skin-like exine remains. Thus, the term “exine-less pollen” sometimes used for similar sporoderm structures in other genera ofZingiberales is misleading and should be substituted by the term “skin-like exine”. Surprisingly, the peculiar pollen wall ultrastructure ofStrelitzia and some otherZingiberales is very similar to that of some genera of theLaurales, an example for convergent evolution within the angiosperms.     

The tubular exine ofLauraceae andHernandiaceae,a novel type of exine structure in seed plants

The pollen grains ofLauraceae andHernandiaceae are characteristic in having a tubular exine of ± microfibrillar structure. This is coated with a layer of medium electron-dense globules and very peculiar spines, made up of a substance differing from that of the exine. Such a pollen wall structure is otherwise unknown in seed plants and thus adds to the list of odd features erratically present in various taxa of the Ranalean complex.     

绣球属(Hydrangea L.)及近缘属花粉形态的研究

为深入研究绣球属植物花粉形态的分类学价值和系统学意义,厘清绣球属与近缘属之间的系统发育关系,该文利用扫描电子显微镜(SEM,scanning electron microscope)对国产绣球属及其近缘属41种绣球花科(Hydrangeaceae)植物的花粉形态以及表面纹饰进行了观察。结果表明:绣球属及其近缘属的花粉为三孔沟;形状多数为长圆体形或近球体形;赤道面观为椭圆形或圆形;极面观多为圆形,少数为三角形或圆三角形。花粉外壁纹饰可分为网状和孔穴状。网眼内的三级纹饰可分为光滑和具颗粒状突起。根据花粉形状和外壁纹饰类型将上述物种划分为4个组,即花粉的形状为长圆体形,表面纹饰为孔穴纹饰;花粉的形状为长圆体形,表面纹饰为网状纹饰;花粉的形状为近球体形,表面纹饰为孔穴纹饰;花粉的形状为近球体形,表面纹饰为网状纹饰。以上可进一步细分为8个类型。上述表明花粉形态证据可为绣球属及其近缘属的属下分类和种间界定提供重要佐证;但结合前人的系统发育重建分析该属植物花粉形态的系统学意义相对有限,如花粉形态证据对于该属及其近缘种属系统发育树上大支的界定难以提供有力的证据。     

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 Comparative study on pollen exine ultrastructure of Nothofagus and the other genera of Fagaceae

The genus Nothofagus is mainly distributed in South America and New Zealand. The present paper describes its pollen exine ultrastructure and compares the exine ultrastructure with that of the other genera of Fagaceae. The pollen grains were examined using ultrathin sectioning technique under transmission electron microscope. The study shows that the pollen exine ultrastructure of Nothofagus differs from that of the other genera of Fagaceae by its exine structure and thickness, type of aperture, and ornamentation. The pollen exine of Nothofagus is thin and possesses granular bacules, regular foot layer and tectum, spinulate ornamentation, and the endexine is usually visible at poral area, and 5～8 colpate. The pollen exine of the other genera of Fagaceae possesses entire bacules, irregular foot layer and tectum, granulate and tuberculate ornamentation, thicker endexine, and is 3-colporate ( 3-colpate or 3-colporoidate). The pollen exine ultrastructure of Nothofagus may belong to primitive type. The pollen exine ultrastructure data support Kuprianova’s opinion that Nothofagus should be separated from Fagaceae and established as a monogenetic family, i.e. Nothofa-gaceae.     

Pollen germination in Welwitschia mirabilis Hook. f.: differences between the polyplicate pollen producing genera of the Gnetales

Pollen grains of the seed plant genera Ephedra L. and Welwitschia Hook. f. (Gnetales) are of similar size, shape, and have a polyplicate exine with alternating thicker and thinner regions. Ephedra pollen is considered inaperturate and the exine is shed during germination, leaving the male gametophyte naked. The shed exine curls up and forms a characteristic structure with transverse striations. Such upcurled exines have been found in situ in Early Cretaceous seeds with affinities to Ephedra. The purpose of this study was to document the germination of Welwitschia pollen and investigate whether they also discard their exine during this process.

The pollen grains of Welwitschia are monoaperturate with a distinct, distal sulcus. During germination, the sulcus splits open and the gametophyte expands to a spherical form that extends out of the exine. The pollen tube starts to grow one or two hours later and as in Ephedra, it is displaced towards one side. The exine is not shed but remains as a “cap” that partly covers the male gametophyte. Thus, in this respect the germination process is distinctly different from that in Ephedra and this study demonstrates that discharging the exine during pollen germination is unique to Ephedra, among the polyplicate pollen producing genera in the Gnetales.     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen:Ranunculaceae,Hamamelidaceae, Platanaceae undFagaceae

Transfer of fresh pollen either by wind or by insects is strongly related to the degree of its stickiness. The sticky substances involved should be understood as pollenkitt. Ultrastructural investigations indicate that the sticky pollen of entomophilous angiosperms (in this publicationHamamelis vernalis andH. virginiana, Corylopsis platypetala) results from the deposition of usually electron-dense, homogeneous pollenkitt mainly on the outside layer of the exine. In contrast, the pollen of anemophilous angiosperms (in this publicationParrotia persica, Platanus orientalis, Thalictrum flavum andQuercus robur), but also of some entomophilous angiosperms with special pollination ecology (e.g.Aquilegia vulgaris) is rather dry and powdery. In these cases the pollenkitt often is electron-transparent and inhomogeneous and is mainly removed into the cavities of the exine. Ultrastructure and deposition of pollen and pollenkitt in ambophilous angiosperms (in this publicationThalictrum minus, Castanea sativa) are ± intermediate.

     

Sporoderm in Populus and Salix

Four phenomena were observed in a study of Populus tremula and P. tremula f. gigas microspores from before microspore mitosis through mature pollen which may have general significance in the ontogeny of pollen grains: 1) The exine and orbicules (Ubisch bodies) were covered by membranes. 2) The exine and the tapetal surfaces where orbicules form were covered by a polysaccharide (PAS positive) coat until after microspore mitosis; subsequently the tapetum became plasmodial. 3) Material having the staining characteristics of the nexine 2 (endexine in the sense of Fægri) accumulated on membranes in microspores in the space between the exine and the plasma membrane. That material was almost completely gone from the wall in mature pollen. The membranes on which material had accumulated migrated through the exine. Following passage through the exine these membranes were seen as empty fusiform vesicles in micrographs of anthers prepared by commonly used methods. 4) At about microspore mitosis when the cellulosic intine begins to form, microtubules about 240 A in diameter occurred near the plasma membrane and generally parallel with it. Positive acid phosphatase reactions in tapetal cells together with the morphology of orbicules and other tapetal organelles suggest that the wall of orbicules, which is like the pollen exine, may form as a residual product of a lysosome system.

Sections of mature Salix humilis pollen were compared with Populus.     

Pollen morphology and ultrastructure of selected species of Magnoliaceae

The pollen morphology and ultrastructure of 20 species, representing eight genera of the Magnoliaceae are described based on observations with light, scanning and transmission electron microscopy. The family represents a homogeneous group from a pollen morphological point of view. The pollen grains are boat-shaped with a single elongate aperture on the distal face. The tectum is usually microperforate, rarely slightly or coarsely rugulose. Columellae are often irregular, but well-developed columellae do occur in some taxa. The endexine is distinct in 14 species, but difficult to discern in the genera Parakmeria, Kmeria and Tsoongiodendron. Within the aperture zone the exine elements are reduced to a thin foot layer. The intine has three layers with many vesicular-fibrillar components and tubular extensions in intine 1. The symmetry of the pollen grains, shape, type of aperture and ultrastructure of the intine show a remarkable uniformity in the family. Nevertheless there is variety in pollen size, ornamentation and the ultrastructure of the exine. The pollen of Magnoliaceae is an example of an early trend of specialization, and supports the view that Magnoliaceae are not one of the earliest lines in the phylogeny of flowering plants.     

Orbicules in Betula Pendula and their Possible Role in Allergy

The external morphology, internal structure and stainability for protein of orbicules in Betula pendula are examined by SEM and TEM. The pollen and the orbicule walls stain moderately for protein. The protein is localized mainly at the pollen aperture, in a thin layer between the exine and the intine and in the core and on the surface of the orbicules. The nitrocellulose membrane test indicates possible allergenicity of the orbicules as well as of the pollen. Since the orbicules of Betula pendula are 2–4 um in diameter, they can pass through the bronchiole of the lungs and cause bronchial asthma.     

Pseudointegricorpus clarireticulatum (Samoilovitch) Takahashi: morphology and ultrastructure

Dispersed tricolpate pollen of Pseudointegricorpus clarireticulatum (Samoil.) Takah. from the Upper Maastrichtian in Zeya-Bureya Basin, Amur (Heilongjiang) River area, Russian Far East/China has been studied with light and electron microscopy. Pollen size, pole outlines and the shape of equatorial projections show some variation within the species. The exine is striate-reticulate, semitectate and columellate. The species is characterised by highly complex structures that have harmomegathic function and include equatorial projections, endexinous thickenings, difference in the thickness of the infratectum, foot layer and endexine throughout the pollen grain, and equatorial furrows. Exine layers taper towards colpi regions while they break abruptly in furrow regions. The furrows could have helped to shed the exine quickly and enabled pollen germination. A non-extended region with a small cavity in the ectexine was observed in the equatorial region. We think that this region is characteristic of most Triprojectate species.