Guard cell ontogeny in leaf stomata of the fern Ophioglossum petiolatum

1978 ◽  
Vol 56 (22) ◽  
pp. 2836-2852 ◽  
Author(s):  
R. L. Peterson ◽  
Sarah Hambleton
Keyword(s):  
Cell Wall ◽  
Epidermal Cell ◽  
Guard Cell ◽  
Cell Walls ◽  
Middle Lamella ◽  
Guard Cells ◽  
Aniline Blue ◽  
Blue Staining ◽  
Starch Grains ◽  
Common Cell

Guard cells in Ophioglossum petiolatum leaves are initiated by a single division of a stomatal initial with no subsidiary cells being formed. The stomatal initials have few vacuoles, plastids with little starch, and a large nucleus with much heterochromatin and prominent nucleoli. Young guard cells are similar cytologically to stomatal initials; their common cell walls are thin and traversed by plasmodesmata. Plasmodesmata are also present within guard cell and adjacent epidermal cell walls. With increasing age, guard cells develop a lenticular thickening in the median portion of the common cell walls, larger vacuoles, and plastids with several starch grains. Numerous microtubules are present near the thickening wall which also has an electron-translucent region between the cell wall and the plasmalemma. Many dictyosomes and mitochondria are present in the cytoplasm. Older guard cells become more vacuolated, with some of the vacuoles containing fibrillar or dense deposits. Plastids become very large as a result of storing several large starch grains. In the thickened portion of the cell walls, the middle lamella and some of the adjacent cell wall appear to be degraded during stomatal pore formation. Mature guard cells are highly vacuolated and have very thick electron-dense cell walls without plasmodesmata. Fluorescence microscopy following aniline blue staining shows that aniline blue positive materials are present around and within the thickened portion of the cell walls, at the junction of guard cells with epidermal cells, and as distinct spots in guard cell and epidermal cell walls during the early stages of ontogeny. Mature guard cells, however, lack the distinct fluorescent spots, which are interpreted as plasmodesmata, in their walls.

Nature of the guard cell wall in leaf stomata of three Ophioglossum species

1975 ◽  
Vol 53 (16) ◽  
pp. 1698-1711 ◽  
Author(s):  
R. L. Peterson ◽  
M. S. Firminger ◽  
L. A. Dobrindt
Keyword(s):  
Cell Wall ◽  
Guard Cell ◽  
Cell Walls ◽  
Guard Cells ◽  
Aniline Blue ◽  
Phenolic Substance ◽  
Polarization Microscopy ◽  
Leaf Tissues ◽  
Stomatal Guard Cells ◽  
Staining Techniques

A β-1,3-glucan which has characteristics of callose was identified as a component of the cell wall in stomatal guard cells in three species of the fern, Ophioglossum. This identification was made by the fluorochrome properties of callose when stained with aqueous solutions of aniline blue. Controls involved both the effect of solutions of different pH on autofluorescence of guard cell walls and the extraction of leaf tissues with β-1,3-glucanases before staining with aniline blue. An electron-translucent region between the plasmalemma and the cell wall proper was observed with the electron microscope and corresponded in position with the areas that fluoresced after aniline blue staining.Other components of the guard cell wall identified included cellulose, which was identified by staining techniques, polarization microscopy, and electron microscopy; and a phenolic substance identified by a number of staining reactions. The cell wall failed to stain with a number of reagents for the identification of lignin.

II. On the origin of parasitism in fungi

1905 ◽  
Vol 197 (225-238) ◽  
pp. 7-24 ◽  
Keyword(s):  
Cell Wall ◽  
Host Plant ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Germ Tube ◽  
Guard Cells ◽  
Suitable Host ◽  
Parasitic Fungi ◽  
Germ Tubes ◽  
Gain Access

Respecting the various modes by which parasitic fungi gain access to the interior of the host-plant, much is known. De Bary (1) demonstrated that the germ-tubes of secidiospores and uredospores enter solely through the stomata, whereas germ-tubes of teleutospores, and also those of various other parasites, enter by piercing the walls of the epidermal cells, or of the guard-cells of the stomata. Other fungi gain an entrance sometimes by a stoma, sometimes by piercing the wall of an epidermal cell. The same author also observed that the zoospores of Cytopus and of Peronospora umbelliferarum , when deposited on the leaf of a suitable host-plant, germinate and the germ-tube enters a stoma, whereas when germination takes place in water the germ-tubes soon die. Marshall Ward has shown (2) that in the case of a species of Botrytis an entrance into the host-plant through the cell-walls of the epidermis is effected by means of the secretion of a ferment by the tip of the germ-tube, whereby the substance of the cell-wall is softened.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

Ultrastructural Changes in the Cell Walls of Cambial Derivatives During Wood Formation in Indian ELM (Holoptelea Integrifolia)

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 403-416 ◽  
Author(s):  
Karumanchi S. Rao ◽  
Yoon Soo Kim ◽  
Pramod Sivan
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Ultrastructural Changes ◽  
Cell Wall Polysaccharides ◽  
Lignin Distribution ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Xylem Elements ◽  
S2 Layer

Sequential changes occurring in cell walls during expansion, secondary wall (SW) deposition and lignification have been studied in the differentiating xylem elements of Holoptelea integrifolia using transmission electron microscopy. The PATAg staining revealed that loosening of the cell wall starts at the cell corner middle lamella (CCML) and spreads to radial and tangential walls in the zone of cell expansion (EZ). Lignification started at the CCML region between vessels and associated parenchyma during the final stages of S2 layer formation. The S2 layer in the vessel appeared as two sublayers,an inner one and outer one.The contact ray cells showed SW deposition soon after axial paratracheal parenchyma had completed it, whereas noncontact ray cells underwent SW deposition and lignification following apotracheal parenchyma cells. The paratracheal and apotracheal parenchyma cells differed noticeably in terms of proportion of SW layers and lignin distribution pattern. Fibres were found to be the last xylem elements to complete SW deposition and lignification with differential polymerization of cell wall polysaccharides. It appears that the SW deposition started much earlier in the middle region of the fibres while their tips were still undergoing elongation. In homogeneous lignin distribution was noticed in the CCML region of fibres.

scholarly journals Domain-specific and cell type-specific localization of two types of cell wall matrix polysaccharides in the clover root tip.

1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cellular Differentiation ◽  
Cortical Cell ◽  
Middle Lamella ◽  
Root Cap ◽  
Root Tip ◽  
Cortical Cells ◽  
Peripheral Cell ◽  
Clover Root

Using immunocytochemical techniques and antibodies that specifically recognize xyloglucan (anti-XG), polygalacturonic acid/rhamnogalacturonan I (anti-PGA/RG-I), and methylesterified pectins (JIM 7), we have shown that these polysaccharides are differentially synthesized and localized during cell development and differentiation in the clover root tip. In cortical cells XG epitopes are present at a threefold greater density in the newly formed cross walls than in the older longitudinal walls, and PGA/RG-I epitopes are detected solely in the expanded middle lamella of cortical cell corners, even after pretreatment of sections with pectinmethylesterase to uncover masked epitopes. These results suggest that in cortical cells XG and PGA/RG-I are differentially localized not only to particular wall domains, but also to particular cell walls. In contrast to their nonoverlapping distribution in cortical cells, XG epitopes and PGA/RG-I epitopes largely colocalize in the epidermal cell walls. The results also demonstrate that the middle lamella of the longitudinal walls shared by epidermal cells and by epidermal and cortical cells constitutes a barrier to the diffusion of cell wall and mucilage molecules. Synthesis of XG and PGA/RG-I epitope-containing polysaccharides also varies during cellular differentiation in the root cap. The differentiation of gravitropic columella cells into mucilage-secreting peripheral cells is marked by a dramatic increase in the synthesis and secretion of molecules containing XG and PGA/RG-I epitopes. In contrast, JIM 7 epitopes are present at abundant levels in columella cell walls, but are not detectable in peripheral cell walls or in secreted mucilage. There were also changes in the cisternal labeling of the Golgi stacks during cellular differentiation in the root tip. Whereas PGA/RG-I epitopes are detected primarily in cis- and medial Golgi cisternae in cortical cells (Moore, P. J., K. M. M. Swords, M. A. Lynch, and L. A. Staehelin. 1991. J. Cell Biol. 112:589-602), they are localized predominantly in the trans-Golgi cisternae and the trans-Golgi network in epidermal and peripheral root cap cells. These observations suggest that during cellular differentiation the plant Golgi apparatus can be both structurally and functionally reorganized.

Ultrastructure des parois de cerises Bigarreau Burlat de textures différentes au cours de la maturation

1996 ◽  
Vol 74 (12) ◽  
pp. 1974-1981 ◽  
Author(s):  
C. Batisse ◽  
P. J. Coulomb ◽  
C. Coulomb ◽  
M. Buret
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Primary Cell ◽  
Wall Material ◽  
Cell Wall Degradation ◽  
Composition And Structure ◽  
Cell Wall Texture ◽  
Synthesis And Degradation ◽  
Soft Fruits

The changes in texture of fruits during ripening are linked to cell wall degradation involving synthesis and degradation of polymers. An increase in pectin solubility leads to cell sliding and an elastic aspect of tissues. The biochemical cell wall process differs between soft and crisp fruits originating from a same cultivar but cultivated under different agroclimatic conditions. Although the proportions of cell wall material are similar, the composition and structure of the two cell walls are very different at maturity. A solubilization of the middle lamella and a restructuration of the primary cell walls arising from the cells separation is observed in crisp fruits. In contrast, the middle lamella of the soft fruits is better preserved and the primary cell walls are thin and show degradation bags delimited by residual membrane formations. In addition, the macroendocytosis process by endosome individualization is more important in soft fruits. In conclusion, the fruit texture depends on the extent of the links between cell wall polymers. Keywords: cherry, cell wall, texture, ultrastructural study.

Microdistribution of copper in copper-ethanolamine (Cu-EA) treated southern yellow pine (Pinus spp.) related to density distribution

Holzforschung ◽  
2005 ◽  
Vol 59 (1) ◽  
pp. 82-89 ◽  
Author(s):  
Jinzhen Cao ◽  
D. Pascal Kamdem
Keyword(s):  
Cell Wall ◽  
Density Distribution ◽  
Cell Walls ◽  
Middle Lamella ◽  
Treated Wood ◽  
Yellow Pine ◽  
Using Data ◽  
Pinus Spp ◽  
Southern Yellow Pine ◽  
The Relationship

Abstract The relationship between copper absorption and density distribution in wood cell walls was investigated in this study. The density distribution on layer level was obtained from two approaches: (1) calculation by using data obtained from literature; (2) microdistribution of carbon and oxygen atoms in the wood cell. The microdistribution of carbon and oxygen in untreated southern yellow pine (Pinus spp.) sapwood, as well as copper in cell walls of copper-ethanolamine (Cu-EA) treated wood was determined by scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM-EDXA). Both approaches for density distribution led to the same result: the density was higher in the compound middle lamella and cell corners than in the secondary wall. The concentration/intensity of Cu, C and O in the cell wall follow the same trend as the density distribution; suggesting that density may play a major role in SEM-EDXA study of the distribution of metal-containing wood preservatives within the wood cell wall.

Ultrastructural observations on guard cells of Vicia faba and Allium porrum

1972 ◽  
Vol 50 (6) ◽  
pp. 1405-1413 ◽  
Author(s):  
W. G. Allaway ◽  
George Setterfield
Keyword(s):  
Vicia Faba ◽  
Small Groups ◽  
Guard Cell ◽  
Cell Walls ◽  
Guard Cells ◽  
Cell Physiology ◽  
Allium Porrum ◽  
Starch Granules ◽  
Mesophyll Cells ◽  
Guard Cell Chloroplasts

Stomata of Vicia faba and Allium porrum were examined in thin section with the electron microscope. Guard cells contained numerous mitochondria, few plastids, and relatively small vacuoles traversed by many strands of cytoplasm. Spherosomes were often observed but were variable in occurrence. Endoplasmic reticulum and dictyosomes were present, although not well developed. Scattered microtubules were present at the periphery of the cells. Microbodies were very rarely observed in guard cells and no plasmodesmata were ever seen in the guard cell walls. Plastids were small and irregular in outline in guard cells of both species. Guard cell plastids of V. faba contained abundant large starch granules. In both species thylakoids were few and grana were small in comparison with mesophyll plastids. The inner of the two bounding membranes of guard cell chloroplasts was extensively invaginated, forming a peripheral reticulum. This was not observed in mesophyll plastids of these species. Small groups of microtubule-like structures were often observed in V. faba guard cell plastids; microtubule-like structures were less frequent in A. porrum plastids, and were not in groups. The structures described are compared with those of other epidermal cells and mesophyll cells, and are discussed in relation to guard cell physiology.

scholarly journals Chilling Injury in Peaches: A Cytochemical and Ultrastructural Cell Wall Study

1992 ◽  
Vol 117 (1) ◽  
pp. 114-118 ◽  
Author(s):  
J.G. Luza ◽  
R. van Gorsel ◽  
V.S. Polito ◽  
A.A. Kader
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Prunus Persica ◽  
Periodic Acid ◽  
Chilling Injury ◽  
Middle Lamella ◽  
Wall Structure ◽  
Positive Staining ◽  
Intercellular Matrix ◽  
Parenchyma Cells

Fruits of mid- (`O'Henry'), late (`Airtime'), and extra-late-season (`Autumn Gem') peach [Prunus persica (L.) Batsch] cultivars were examined for changes in cell wall structure and cytochemistry that accompany the onset of mealiness and leatheriness of the mesocarp due to chilling injury. The peaches were stored at 10C for up to 18 days or at SC for up to 29 days. Plastic-embedded sections were stained by the Schiff's-periodic acid reaction, Calcofluor white MR2, and Coriphosphine to demonstrate total insoluble carbohydrates, ß-1,4 glucans, and pectins, respectively. Mealiness was characterized by separation of mesocarp parenchyma cells leading to increased intercellular spaces and accumulation of pectic substances in the intercellular matrix. Little structural change was apparent in the cellulosic component of the cell walls of these fruits. In leathery peaches, the mesocarp parenchyma cells collapsed, intercellular space continued to increase, and pectin-positive staining in the intercellular matrix increased greatly. In addition, the component of the cell walls that stained positively for ß-1,4 glucans became thickened relative to freshly harvested or mealy fruit. At the ultrastructural level, dissolution of the middle lamella, cell separation, irregular thickening of the primary wall, and plasmolysis of the mesocarp parenchyma cells were seen as internal breakdown progressed.

scholarly journals ELECTRON-OPAQUE FIBRILS AND GRANULES IN AND BETWEEN THE CELL WALLS OF HIGHER PLANTS

1972 ◽  
Vol 53 (3) ◽  
pp. 695-703 ◽  
Author(s):  
Gary G. Leppard ◽  
J. Ross Colvin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cultured Cells ◽  
Higher Plants ◽  
Middle Lamella ◽  
Woody Species ◽  
Morning Glory ◽  
Plant Cell Walls ◽  
Higher Plant ◽  
Cell Wall Matrix

The components of higher-plant cell walls which become electron-opaque after staining with ruthenium-osmium were studied by electron microscopy. A fibrillar material which absorbs this stain is a major wall constituent in the root epidermal cells of carrot and morning glory. In both form and size, these fibrils resemble those found on the surface of suspension-cultured cells of the same species Some cells of woody species show an irregular distribution of electron-opaque material in the cell wall matrix and middle lamella. This material, which has an amorphous appearance with many electron stains, is shown by ruthenium-osmium staining to be an aggregate of discrete granules, 150–220 A in diameter. These observations are not consistent with the concept of the cell wall matrix and middle lamella as an amorphous, uniform gel

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