Spore wall ultrastructure in the liverwort Fossombronia longiseta

1984 ◽  
Vol 62 (9) ◽  
pp. 1871-1879 ◽  
Author(s):  
M. P. Steinkamp ◽  
W. T. Doyle

Mature spores of Fossombronia longiseta (Metzgeriales, Codoniaceae) were examined with both scanning and transmission electron microscopes. Sporoderms are highly sculptured. The distal face markings consist of parallel ridges (cristae) or spines. The flattened proximal face has a series of short spinelike cristae, and a triradiate ridge mark sometimes is apparent. In section, the sporoderm consists of an intine and a two-layered exine. The inner exine layer consists of two lamellae, each of which contains a series of long, thin (3–4 nm), closely spaced, electron-lucent subunits; the subunits are separated by electron-dense material. The more or less solid outer exine consists of highly irregularly shaped lamellae, which also have a "white line" component. Amorphous, electron-dense material permeates these lamellae and fills the channels between the lamellae. The intine and much of the electron-dense material of the exine is removed by acetolysis. Spore wall ultrastructure in this species is complex compared with other species of the Metzgeriales and Jungermanniales that have been studied so far.

Author(s):  
Y. R. Herd ◽  
E. G. Cutter ◽  
I. Watanabe

SynopsisMicrosporogenesis in cultured material of Azolla microphylla was studied with the light and transmission electron microscopes. The first formed sporangium, a megasporangium, aborts and several microsporangia develop below. Initially, a single sporogenous cell is present, surrounded by a single layered tapetum and the microsporangial wall. Subsequently, several sporogenous cells are connected by plasmodesmata. The microspore mother cells are less densely cytoplasmic than the tapetal cells. Callose-like material is deposited around the microspore mother cells, but disappears before meiosis. The tetrads of microspores contain well defined organelles but less dense cytoplasm than the surrounding periplasmodium. Electron dense material deposited on the plasma membrane of the microspores eventually forms the endospore. The unornamented exospore develops by continued deposition of electron dense material. Degeneration of the periplasmodium gives rise to membranous material which appears to form a template for the massulae.


2010 ◽  
Vol 55 (1) ◽  
Author(s):  
Lenka Šípková ◽  
Céline Levron ◽  
Mark Freeman ◽  
Tomáš Scholz

AbstractSpermiogenesis and spermatozoon ultrastructure of the tapeworm Parabothriocephalus gracilis were described using transmission electron microscopy (TEM). Spermiogenesis is characterized by the formation of a zone of differentiation with two centrioles associated with striated rootlets, and an intercentriolar body between them. The two flagella undergo a rotation of 90° until they become parallel to the median cytoplasmic extension with which they fuse. Electron-dense material is present in the apical region of the zone of differentiation in the early stages of spermiogenesis. This electron-dense material is characteristic for the orders Bothriocephalidea and Diphyllobothriidea. The mature spermatozoon contains two axonemes of the 9 + ‘1’ trepaxonematan pattern, nucleus, parallel cortical microtubules and electron-dense granules of glycogen. The anterior extremity of the spermatozoon exhibits a single helical electron-dense crested body 130 nm thick. One of the most interesting features is the presence of a ring of cortical microtubules surrounding the axoneme. This character has been reported only for species of the order Bothriocephalidea and may be unique in this cestode group.


1988 ◽  
Vol 66 (6) ◽  
pp. 1129-1134 ◽  
Author(s):  
S. F. Hwang ◽  
M. E. Neuwirth ◽  
K. F. Chang

The surface markings of the spores from the aecial, uredinial, and telial stages of Uromyces trifolii-repentis Liro on leaves and petioles of small white clover (Trifolium repens L.) were examined using scanning and transmission electron microscopes. The short, cylindrical aecium was borne within a peridium which was one cell layer thick. The peridial cells were rhomboidal with irregular club-shaped ornaments. The yellowish aeciospores were densely ornamented with smooth, knoblike verrucae. Thin areas of the spore wall were differentiated into germ pores. Two or three germ pores were equatorially arranged on the golden-brown urediniospores, which except for a circular hilar region were evenly covered with minute conical spines. The spines were situated singly in very shallow depressions surrounded by circular ridges. The dark-brown teliospores had smooth walls with a few linearly arranged fine warts, and the walls were thicker at the apex than on the side. A pale papilla covered the germ pore at the apex of the teliospore, which was borne singly on the fragile pedicel.


2010 ◽  
Vol 82 (2) ◽  
pp. 341-352 ◽  
Author(s):  
Cecilia Macluf ◽  
Marta Morbelli ◽  
Gabriela Giudice

The morphology and wall ultrastructure of megaspores and microspores of Isoetes sehnemii that grows in Brazil were analyzed as part of the study of the Isoetaceae present in Southern South America. The observations were performed with light, scanning and transmission electron microscopes. The megaspores are trilete, 350-450μm in equatorial diameter. The surface is reticulate. In section, the sporoderm is 100μm thick including the ornamentation. The wall is composed of a siliceous perispore, which consists of short fused flatten, elements forming a three-dimensional mesh. The exospore has two zones of different structure. The endospore is fibrillar. The microspores are monolete, 21-27μm in equatorial diameter. The sporoderm is composed of a sporopollinic rugulate perispore. A space between the paraexospore and the exospore is evident. The exospore is compact. The endospore is fibrillar. The ultrastructural analysis akes hoologies evident concerning structure and organization of the layers belo the perispore in both spore types. A possible similarity and stability in the ultrustructure of the present spores and fossils could be also inferred. In addition, there would be a correlation among the plant habitat, the spore ornamentation and the geographic distribution.


Nematology ◽  
2003 ◽  
Vol 5 (2) ◽  
pp. 307-312
Author(s):  
Dianne Achor ◽  
Larry Duncan ◽  
Renato Inserra ◽  
Alberto Troccoli

AbstractMature female Gracilacus latescens are sedentary and remain attached by the stylet to the surface of timber bamboo roots (Phyllostachys bambusoides) for their entire life. Observations by transmission electron microscopy (TEM) of the anatomy of the anterior portion of the female body showed the stylet shaft surrounded by a thick stomatal wall sensu Endo (1983) and by large protractor muscles. Cross sections of the root at the site of nematode attachment showed accumulation of electron-opaque material between the nematode body and the epidermal wall penetrated by the stylet. Electron-dense material enwrapped the stylet from the point of its insertion in an epidermal cell wall until its end in the lumen of a sclerenchymal or cortical cell. Two to three cells are penetrated by the stylet. The electron-dense material appeared to originate from the walls of epidermal, cortical parenchymal and sclerenchymal cells perforated by the stylet. The thickness of this material increased with the number of sclerenchyma cell walls penetrated by the stylet. Cross sections of the enwrapped stylet showed it tightly encased in the electron-dense material, which appeared to anchor the stylet and consequently the nematode body to the root surface. A syncytium originates from the innermost cell reached by the enwrapped stylet and expands into the inner cortex and stele. Cell wall dissolution and pit fields are characteristics of the syncytium.


2003 ◽  
Vol 40 (2) ◽  
pp. 149-156 ◽  
Author(s):  
C. Arraga-Alvarado ◽  
M. Palmar ◽  
O. Parra ◽  
P. Salas

Since 1982 Ehrlichia platys, now emended as Anaplasma platys, has been diagnosed in dogs from Maracaibo, Venezuela, using buffy coat smears stained with Dip Quick. Three dogs were inoculated with an A. platys strain. When parasitemia reached 60–97%, blood samples obtained from the inoculated dogs and from two naturally infected dogs were centrifuged to obtain platelet-rich plasma, which was mixed with 0.1% glutaraldehyde at 37 C for 10 minutes. Platelet pellets were fixed in 3% glutaraldehyde for 72 hours and processed for conventional transmission electron microscopy. Platelets contained pleomorphic organisms with a distinct double membrane that was not observed when the bodies were in a determinate developmental stage. There were 1–15 individual bodies included in a host cell vacuole. The organisms had an electron-lucent inner area, whereas the internal surface of their inner plasma membranes exhibited an electron-dense rough substance. In naturally infected dogs, organisms with different ultrastructural features were found inside the same platelet. Some organisms contained central dense material surrounded by a pale zone, which was in turn surrounded by a moderately dense peripheral area. Other organisms contained an eccentrically electron-dense material. The intravacuolar space appeared fully electron-lucent. Each organism usually exhibited inner fine strands. Empty structures displaying junctions with the vacuolar membrane were observed. Our results indicate that distinct ultrastructural characteristics are associated with different stages of A. platys development and may differ among A. platys strains.


1989 ◽  
Vol 37 (7) ◽  
pp. 981-987 ◽  
Author(s):  
M Grote

The exine of birch pollen was examined by scanning and transmission electron microscopy in the native state and after fixation in different aqueous fixatives: glutaraldehyde + OsO4; glutaraldehyde + cetylpyridinium chloride (CPC) + OsO4; glutaraldehyde + cuprolinic blue (CB); and periodate + lysine + paraformaldehyde (PLP). The native pollen exine showed a thin (3-5-nm) border of electron-dense material lining the tectum and electron-dense material within microchannels and bacula cavities. Fixation with the addition of CPC resulted in a voluminous surface coat surrounding the pollen grain, but empty microchannels and bacula cavities. After fixation with the addition of CB, there was a thin surface coat, whereas microchannels and bacula cavities were partially filled with electron-dense material. The other fixatives led to empty microchannels and bacula cavities. There was no surface coat on the pollen grain. However, after all fixation procedures, a thin electron-dense border of the tectum remained visible. Concerning the electron-dense material filling microchannels and bacula cavities in the native pollen grain, the results obtained in the present study suggest that it is either completely lost (after conventional and PLP fixation) or, after fixation with a precipitating additive, partially (CB) or completely (CPC) solubilized and precipitated on the surface of the pollen grain as a surface coat.


2011 ◽  
Vol 48 (3) ◽  
pp. 174-183 ◽  
Author(s):  
L. Poddubnaya ◽  
N. Pospekhova

AbstractThis study was designed to provide information on the ultrastructural traits of the cirrus sac of the male strobila of the dioecious cyclophyllidean tapeworm, Shipleya inermis Fuhrmann, 1908 from the small intestine of long-billed dowitchers, Limnodromus scolopaceus, in Chukotka, Russia. The cirrus sac is characterised by a thick muscular wall (comprising about 20 layers of longitudinal muscles) with the muscle cells being located outside the wall along the peripheral muscle layer and the presence of a thick, fibrillar septum inside the sac along the inner muscle layer of the wall. The epithelium of the intrabursal ducts is syncytial and has sunken perikarya. The ejaculatory duct is characterised by surface luminal microvilli and a large number of the sunken perikarya producing electron-dense secretory granules, which discharge into the duct lumen as an apocrine secretion. The cirrus is armed with two types of sclerotized structures formed by its epithelium, hooks of about 25 μm in length and microthrix-like structures on its luminal surface. The hooks are sigmoid in shape, have a blade circular in transverse section and about 3.5 μm in width, and taper at both extremities. The hook body consists of moderately electron-dense material mixed with a more electron-dense material and an electron-lucent core. The hook roots lie within the cirrus epithelium, where their lateral margins are composed of a thin covering of electrondense material with narrow lateral extensions. The usefulness of the ultrastructural characters of the cirrus sac as indicators of phylogenetic relationships within the Eucestoda is discussed.


1985 ◽  
Vol 117 (1) ◽  
pp. 87-110
Author(s):  
T.D. SCHULTZ ◽  
M.A. RANKIN

Tiger beetles of the genus Cicindela exhibit iridescent structural coloration due to the presence of a non-ideal multilayer interference reflector located in the outermost 2 μm of the integument. The reflector is composed of alternating layers of electron-lucent and electron-dense material. This series of layers was distinguished from chitinous procuticle by its position, ultrastructure and solubility in dilute KOH. The reflector appears homologous with the inner epicuticle of current models. Measurements of surface reflectance, refractive index and the dimensions of the alternating layers suggests that the dense layer has a refractive index (RI) near 2.0 and may be a melanoprotein.


1998 ◽  
Vol 353 (1378) ◽  
pp. 1983-2004 ◽  
Author(s):  
C. H. Wellman ◽  
D. Edwards ◽  
L. Axe

Spore masses and isolated sporangia, containing laevigate hilate cryptospores attributable to the dispersed taxon Laevolancis divellomedia sensu lato , have been recovered on bulk maceration of Upper Silurian (Pridoli) and Lower Devonian (Lochkovian) deposits from the Welsh Borderland. Detailed morphological, anatomical and ultrastructural analysis, using light microscope, scanning electron microscope and transmission electron microscope techniques, reveals subtle differences between the specimens and they can be grouped into five distinct types. The different groups are distinguished principally by using sporangia–spore mass characteristics, presence or absence of extra–exosporal material and nature of spore–wall ultrastructure. Of the groups, one has a uniformly homogeneous exospore and the other four groups have a bilayered exospore. In the former the spores lack extra–exosporal material and occur in a discoidal sporangium. Of the bilayered groups, two have exospores of homogeneous composition but with the two layers differing in electron density. They occur in discoidal sporangia and spore masses and are distinguished on the presence or absence of extra–exosporal material and differences in the widths of the two layers. Finally, two bilayered groups possess a lamellate inner layer, but vary in presumed sporangial shape. Elongate sporangia have spores with concentric continuous lamellae, lacking further ultrastructure. In contrast, spores from a discoidal spore mass have white–line–centred, presumably tripartite, lamellae which are laterally discontinuous, overlapping and irregularly spaced. These findings, which suggest that morphologically similar spores were produced by a number of plant taxa, have important implications regarding the assessment of early land–plant diversity. The affinities of hilate cryptospore–producing plants are unknown and problematic, particularly as no extant non–angiosperm plants produce dyads, other than through meiotic irregularity, and spore–sporangial characters have no exact counterpart in coeval plants. Studies of specimens with in situ hilate cryptospores suggest that they derive from rhyniophytoids, i.e. plants that resemble the simplest of vascular plants but lack evidence of vascular tissue, although hilate cryptospore–containing examples show no axial branching. It might be argued, based on evidence from spore wall ultrastructure, that some of the plants have more in common with lycopsids and filicopsids than bryophytes, a surprising finding bearing in mind the stratigraphic distribution of hilate cryptospores–dyads and inferences that the producers were bryophyte–like. Detailed studies of wall structure in the hilate cryptospores permit consideration of spore wall development. It is suggested that extra–exosporal material derives from a tapetum and is thus produced by the diploid sporophyte. The white–line–centred lamellae in a single specimen provide the earliest evidence for the presence of such structures in early land plant spores and provide further evidence that sporopollenin deposition on such structures is the most primitive mode of sporopollenin deposition among land plants.


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