Ectodesmata as Revealed By Freeze-Etch Preparations of Plant Epidermal Cell Walls

Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.

Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


2017 ◽  
pp. 66
Author(s):  
Aída Carrillo-Ocampo ◽  
E.M. Engleman

With methods of light microscopy, histochemical staining and scanning electron microscopy, it was found that the ovule in the seed of Tigridia pavonia (Iridaceae) is anatropous, bitegmic, and crassinucellate. During development, the exotegmen is crushed and the endotegmen persists with tannins in the lumens and in the walls, which also react positively for lignin. The exotesta contains tannins and its outer walls are convex, thickened, and cuticularized. The mesotesta has multiple layers, accumulates abundant lipids, and forms a bulge in the chalaza. The cell walls of the endotesta collapse and accumulate tannins. In the chalaza, a hypostasal cushion contains tannins in the lumens and in the walls, which also react positively for lignin. At the micropylar end of the seed there is an operculum which consists of: a) a slightly crushed exotegmen, b) an endotegmen with cuticular thickenings that are concentric with respect to the micropyle, c) hemispherical deposists of cutin on the anticlinal walls of the endotegmen, and c) a thin layer of endosperm that covers the radicle. During its cellular stage of development, the endosperm has conspicuous transfer walls at the chalazal end next to the nucella. The embryo is small and has a conical cotyledon.


1963 ◽  
Vol 16 (4) ◽  
pp. 768 ◽  
Author(s):  
MS Buttrose

The developing aleurone layer cells of the wheat kernel have been investigated by electron microscopy and the results compared with those of light microscopy. Two weeks after flowering vacuoles appear in the cells and deposits accumulate in these until maturity when the cells are filled 'with the resulting "vacuolar units" 2-3p. in diameter, corresponding to the aleurone grains of light microscopy. The wheat aleurone grain consists of a bounding membrane (of vacuole origin) enclosing a matrix in which are embedded spherical deposits. Some of these deposits are translucent and others opaque to electrons after potassium permanganate and osmium tetroxide fixation. At all stages examined the cytoplasm of aleurone cells contained large numbers of small unidentified bodies with irregular outline and dense contents. At first they are dispersed, but towards maturity are organized as a monolayer over the surface of each aleurone grain and the inner surface of the cell walls. The apparent specificity of these structures to aleurone cells is discussed in relation to future chemical and physiological studies of the tissue.


1985 ◽  
Vol 54 (2) ◽  
pp. 304-317 ◽  
Author(s):  
H. Kolb ◽  
J. Jones

Red and green cones of two turtle species (Pseudemys scripta elegans and Chelydra serpentina) retina have been stained with Golgi procedures and examined by light microscopy of whole-mount tissue and by electron microscopy of serial thin sections. By light microscopy, red and green single cones appear indistinguishable, but double cones can be readily identified. All Golgi-stained photoreceptors in turtle retina have a spray of telodendria radiating from their synaptic pedicles. The telodendria of single cones are 10-20 micron long and end in clusters of terminals, whereas double cones have 30- to 50-micron long telodendria in addition to a very short bush of telodendria arising from one side of the pedicle. Electron microscopy of the Golgi-stained cones allows them to be distinguished into red or green spectral types by the appearance of their oil droplets. Furthermore, the spectral identity of cones contacted by the telodendria of identified Golgi-stained cones can similarly be determined. Red single cones make telodendrial contacts with other red singles, both members of the double cones, and with green single cones. Green single cones likewise connect to many surrounding red cones, both single and double types, and a few other green singles. Both members of the double cone connect to neighboring red and green singles and occasionally to double cones. The telodendria of stained cones end on spectrally homologous or heterologous cone types at basal junctions, central elements of ribbon synapses or, sometimes, as lateral elements of ribbon synapses. However, all these synaptic contacts appear to be of the same type, i.e., narrow-cleft basal junctions. Small gap junctions occur between neighboring cone pedicles, regardless of spectral type, in the visual streak area of the retina. Large gap junctions occur between unidentified cone telodendria in the neuropil of the outer plexiform layer. The telodendrial connections between red and green cones in the turtle retina have the appearance of chemical synapses and suggest an anatomical pathway responsible for the mixing of red and green signals in red or green cones of the turtle retina as reported in the accompanying physiological paper by Normann, Perlman, and Daly (27).


1985 ◽  
Vol 63 (4) ◽  
pp. 757-761 ◽  
Author(s):  
E. Untiedt ◽  
K. Müller

Lyophyllum palustre (Peck) Singer, a basidiomycete (Tricholomataceae) parasitizing Sphagnum, was examined for points of contact between hyphae and Sphagnum cells with the help of light microscopy, scanning electron microscopy, and transmission electron microscopy. Results indicate that the fungus attacks Sphagnum cells by penetrating cell walls and altering host cell protosplasm. In addition, the formation of additional partitioning cell walls in attacked living Sphagnum cells was observed.


1984 ◽  
Vol 11 (3) ◽  
pp. 179 ◽  
Author(s):  
BA Baldo ◽  
D Barnett ◽  
JW Lee

Fluorescein isothiocyanate-labelled lectin from wheat-gem, which binds N-acetyl-D-glucosamine, and Griffonia simplicifolia, Arachis hypogaea and Glycine max lectins, each of which binds D-galactose, react with nucellar epidermal cell walls in thin sections of plastic-embedded developing wheat grain. Reactivity of these cell walls with periodic acid-Schiff reagent, the absence of staining with protein stains and the failure of a number of proteases and the endoglycosidases D and H to prevent the binding suggested that the lectin-reactive wall components are neither proteins nor N-glycosidically linked glycoproteins. Morphological differences in lectin staining patterns and treatment of sections with chitinase and α-galactosidase, prior to the reaction with the lectins, indicated that two separate polysaccharides are probably involved in the binding. Chitinase removed the reactivity of the nucellar epidermal cell walls for wheat-germ lectin but the binding of D-galactose-specific lectins was unimpaired. Conversely, α-galactosidase did not affect the binding of wheat-germ lectin but reactivity with the galactose-specific lectins was abolished. From the available evidence we conclude that one polysaccharide in the nucellar epidermal cell wall reacts with wheat-germ lectin and contains N-acetyl-D-glucosamine in a chitin-like structure. The other polysaccharide reacts with D-galactose- specific lectins by virtue of terminal α-D-galactose residues. Hydrolysis and subsequent chromatographic analysis of nucellar epidermal cell walls peeled from immature grains revealed the presence of D-glucosamine, D-glucose, D-galactose, D-xylose, L-arabinose and a trace of D-mannose.


Author(s):  
I. Manton ◽  
G. F. Leedale

C. ericina Parke & Manton has been re-investigated to add salient features of micro-anatomy from the electron microscopy of thin sections and also to add photographs of living cells taken with anoptral contrast light microscopy.The most important new observations concern the scales which are shown to be essentially two-layered plates in which the layers in the very large spined scales have become separated except at their edges, with the outer layer greatly hypertrophied to produce a hollow spine with a flared base closed at the bottom by a flat plate. The patterns of external marking on the two layers are very similar in both plate-scales and spines in this species and the orientation of both with respect to the cell surface has been demonstrated by a section of the scales in situ.


1966 ◽  
Vol 44 (6) ◽  
pp. 821-826 ◽  
Author(s):  
J. R. Edwardson ◽  
D. E. Purcifull ◽  
R. G. Christie

Particles within lesions of leaf tissue infected with either tobacco necrosis virus (TNV) or southern bean mosaic virus (SBMV) were compared with particles in embedded pellets of purified preparations of these viruses by an examination of thin sections. The mode of the diameters of particles in tissues and pellets was 20.5 mµ.It is assumed that the particles in infected tissues are virus particles on the basis of their similarities in size, shape, and arrangement with the particles in purified preparations.


1986 ◽  
Vol 64 (12) ◽  
pp. 2909-2915 ◽  
Author(s):  
V. N. Tariq ◽  
P. Jeffries

The infection of leaf and stem tissues of Phaseolus by Sclerotinia sclerotiorum was studied using electron microscopy. Direct entry of the intact plant surface was achieved by hyphae from simple or compound appressoria. A closely appressed hyphal tip developed an electron-lucent region at the apex, in which a plasmalemmal invagination formed. This invagination surrounded a region of extracytoplasmic vesicular material which penetrated the cuticle during invasion. Penetration occurred by a narrow infection peg which passed through the cuticle via a narrow pore and caused little change in cuticle integrity. Once the cuticle was breached, a walled subcuticular vesicle developed from which infection hyphae spread laterally. Destruction of the epidermal cell walls was both rapid and extensive. Leaf and stem colonization occurred by intercellular growth of undifferentiated hyphae accompanied by cellular necrosis in advance of the mycelial front.


1971 ◽  
Vol 19 (2) ◽  
pp. 173 ◽  
Author(s):  
SGM Carr ◽  
L Milkovits ◽  
DJ Carr

The eucalypt leaf contains a store of untapped information of potentially great value taxonomic and evututionary studies. Tie cuticie of certain eucalypts is shown to possess a complex and species-specific ornamentation so distinctive that its features can be regarded as diagnostic. The term "phytoglyph" is coined for the constellation of microanatomical features of the surfaces of leaves, including the microanatomy of the cuticle. Phytoglyphic analysis relates to the combination of three methods, light microscopy of stained cuticles, scanning electron microscopy of leaf surfaces, and light microscopy of thin sections of the cuticular and associated structures. Its use is illustrated by the dissection of the "form species" E. dichromophloia into a number of separate and recognizable entities, some of which were previously accorded the status of species. The plant geographical and other implications of this dissection are dealt with. In particular, E. dichromophloia F. Muell. is to be regarded as a species of very restricted distribution. The microanatomical characters of the cuticle are closely controlled products of the epidermal layers. The fact that specimens which (on other grounds) can be grouped together as a species have identical cuticular microanatomy suggests that the phytoglyph is genetically strongly determined and does not consist of inadvertent, trivial surface features with a high degree of plasticity. This in turn raises the problem of the development of the cuticular microanatomy which cannot be explained on current views of the formation of the cuticle by passive diffusion of precursor substances through the epidermal walls, followed by a hardening process.


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