scholarly journals THE DEVELOPMENT OF THE SECONDARY WALL OF THE XYLEM IN ACER PSEUDOPLATANUS

1964 ◽  
Vol 23 (2) ◽  
pp. 327-337 ◽  
Author(s):  
F. B. P. Wooding ◽  
D. H. Northcote
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Secondary Wall ◽  
Acer Pseudoplatanus ◽  
Undifferentiated Cell ◽  
Glutaraldehyde Fixation ◽  
Specific Relation ◽  
Golgi Bodies ◽  
Thin Skin ◽  
Xylem Element

The development of the spirally thickened xylem element from a cambium initial of sycamore Acer pseudoplatanus has been traced by means of electron microscopy. The narrow elongated cambial initial undergoes considerable expansion in all dimensions. The cytoplasm at this stage is distributed in a thin skin between the cell wall and a large vacuole. No correlation has been observed between the distribution of any organelle and the pattern of the eventual thickenings. After the sites of thickening deposition have become apparent, the most conspicuous feature of the cell is the proliferation of Golgi bodies and vesicles. It is suggested that the material of the developing thickenings stems from direct apposition of the material in the Golgi vesicles. After glutaraldehyde fixation, microtubules (200 to 220 A in diameter) are seen to be sited in specific relation to the thickenings, the orientation of the tubules mirroring that of the fibrils seen in the thickenings. Possible reasons for absence of an observable pattern in the expanded but relatively undifferentiated cell are given, and the possible roles of the Golgi apparatus and microtubules in the thickening production are discussed

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).

Some small-sized Cosmarium (Conjugatophyceae, Desmidiales) from sphagnum bogs of Moscow Region

2013 ◽  
Vol 47 ◽  
pp. 13-20
Author(s):  
O. V. Anissimova
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cell Wall ◽  
Moscow Region ◽  
Biological Station ◽  
Sphagnum Bogs ◽  
Different Seasons ◽  
Scanning Electron

Algae samples were collected during different seasons from 1997 to 2011 in two swamps located at Zvenigorod Biological Station in Moscow Region. There were found 25 Cosmarium species and varieties, 9 taxa of them being new to the region. Descriptions of the taxa were specified by observation of cell wall ornamentation with light and scanning electron microscopy. Original descriptions, photos and drawings of algae are presented.

scholarly journals MYB Transcription Factors and Its Regulation in Secondary Cell Wall Formation and Lignin Biosynthesis during Xylem Development

2021 ◽  
Vol 22 (7) ◽  
pp. 3560
Author(s):  
Ruixue Xiao ◽  
Chong Zhang ◽  
Xiaorui Guo ◽  
Hui Li ◽  
Hai Lu
Keyword(s):  
Cell Wall ◽  
Transcription Factors ◽  
Secondary Wall ◽  
Secondary Cell Wall ◽  
Lignin Biosynthesis ◽  
Cell Wall Formation ◽  
Long Distance ◽  
Secondary Cell Wall Formation ◽  
Myb Transcription Factors ◽  
Wall Formation

The secondary wall is the main part of wood and is composed of cellulose, xylan, lignin, and small amounts of structural proteins and enzymes. Lignin molecules can interact directly or indirectly with cellulose, xylan and other polysaccharide molecules in the cell wall, increasing the mechanical strength and hydrophobicity of plant cells and tissues and facilitating the long-distance transportation of water in plants. MYBs (v-myb avian myeloblastosis viral oncogene homolog) belong to one of the largest superfamilies of transcription factors, the members of which regulate secondary cell-wall formation by promoting/inhibiting the biosynthesis of lignin, cellulose, and xylan. Among them, MYB46 and MYB83, which comprise the second layer of the main switch of secondary cell-wall biosynthesis, coordinate upstream and downstream secondary wall synthesis-related transcription factors. In addition, MYB transcription factors other than MYB46/83, as well as noncoding RNAs, hormones, and other factors, interact with one another to regulate the biosynthesis of the secondary wall. Here, we discuss the biosynthesis of secondary wall, classification and functions of MYB transcription factors and their regulation of lignin polymerization and secondary cell-wall formation during wood formation.

scholarly journals Effect of Exogenously Applied 24-Epibrassinolide and Brassinazole on Xylogenesis and Microdistribution of Cell Wall Polymers in Leucaena leucocephala (Lam) De Wit

2021 ◽  
Author(s):  
S. Pramod ◽  
M. Anju ◽  
H. Rajesh ◽  
A. Thulaseedharan ◽  
Karumanchi S. Rao
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Leucaena Leucocephala ◽  
Higher Plants ◽  
Lignin Content ◽  
Wood Quality ◽  
Wall Structure ◽  
Vessel Element ◽  
Xylem Differentiation ◽  
Cell Wall Polymers

AbstractPlant growth regulators play a key role in cell wall structure and chemistry of woody plants. Understanding of these regulatory signals is important in advanced research on wood quality improvement in trees. The present study is aimed to investigate the influence of exogenous application of 24-epibrassinolide (EBR) and brassinosteroid inhibitor, brassinazole (BRZ) on wood formation and spatial distribution of cell wall polymers in the xylem tissue of Leucaena leucocephala using light and immuno electron microscopy methods. Brassinazole caused a decrease in cambial activity, xylem differentiation, length and width of fibres, vessel element width and radial extent of xylem suggesting brassinosteroid inhibition has a concomitant impact on cell elongation, expansion and secondary wall deposition. Histochemical studies of 24-epibrassinolide treated plants showed an increase in syringyl lignin content in the xylem cell walls. Fluorescence microscopy and transmission electron microscopy studies revealed the inhomogenous pattern of lignin distribution in the cell corners and middle lamellae region of BRZ treated plants. Immunolocalization studies using LM10 and LM 11 antibodies have shown a drastic change in the micro-distribution pattern of less substituted and highly substituted xylans in the xylem fibres of plants treated with EBR and BRZ. In conclusion, present study demonstrates an important role of brassinosteroid in plant development through regulating xylogenesis and cell wall chemistry in higher plants.

The nature of reaction wood. IV. Variations in cell wall organization of tension wood fibres

1955 ◽  
Vol 3 (2) ◽  
pp. 177 ◽  
Author(s):  
AB Wardrop ◽  
HE Dadswell
Keyword(s):  
Cell Wall ◽  
Tension Wood ◽  
Secondary Wall ◽  
Degree Of Crystallinity ◽  
Tropical Species ◽  
Normal Wood ◽  
Reaction Wood ◽  
Gelatinous Layer ◽  
Wood Fibres ◽  
Cell Wall Organization

The cell wall organization, the cell wall texture, and the degree of lignification of tension wood fibres have been investigated in a wide variety of temperate and tropical species. Following earlier work describing the cell wall structure of tension wood fibres, two additional types of cell wall organization have been observed. In one of these, the inner thick "gelatinous" layer which is typical of tension wood fibres exists in addition to the normal three-layered structure of the secondary wall; in the other only the outer layer of the secondary wall and the thick gelatinous layer are present. In all the tension wood examined the micellar orientation in the inner gelatinous layer has been shown to be nearly axial and the cellulose of this layer found to be in a highly crystalline state. A general argument is presented as to the meaning of differences in the degree, of crystallinity of cellulose. The high degree of crystallinity of cellulose in tension wood as compared with normal wood is attributed to a greater degree of lateral order in the crystalline regions of tension wood, whereas the paracrystalline phase is similar in both cases. The degree of lignification in tension wood fibres has been shown to be extremely variable. However, where the degree of tension wood development is marked as revealed by the thickness of the gelatinous layer the lack of lignification is also most marked. Severity of tension wood formation and lack of lignification have also been correlated with the incidence of irreversible collapse in tension wood. Such collapse can occur even when no whole fibres are present, e.g. in thin cross sections. Microscopic examination of collapsed samples of tension wood has led to the conclusion that the appearance of collapse in specimens containing tendon wood can often be attributed in part to excessive shrinkage associated with the development of fissures between cells, although true collapse does also occur. Possible explanations of the irreversible shrinkage and collapse of tension wood fibres are advanced.

Ultrastructure of Medicago sativa rhizodermis cells over their early development

Biologia ◽  
2008 ◽  
Vol 63 (2) ◽  
Author(s):  
Lucia Mikolajová ◽  
Halina Vargová ◽  
Zora Hanáčková ◽  
Milada Čiamporová
Keyword(s):  
Cell Wall ◽  
Medicago Sativa ◽  
Root Hair ◽  
Phosphotungstic Acid ◽  
Root Tip ◽  
Cell Wall Polysaccharides ◽  
Golgi Bodies ◽  
Internalization Process ◽  
Subcellular Level ◽  
Root Hair Initiation

AbstractUltrastructure was investigated along the files of developing epidermal cells in the root tip of a model plant Medicago sativa, in which all rhizodermal cells are potential hair-forming trichoblasts. Differentiation at subcellular level was observed up to the stage of bulge initiation in the trichoblasts. Root hair initiation indicated by the emergence of bulges from trichoblasts was detected at various distances from the root tip and, it was independent of the trichoblast size.During rhizodermal cell differentiation, starch grains accumulated in the plastids. Nuclei located in the central part of the young, meristematic cells moved towards the inner periclinal wall as the central vacuole enlarged. The bulging region of the trichoblasts located opposite the nucleus and was rich in mitochondria, ER, ribosomes, and Golgi bodies, and contained also vesicles enclosing fibrillar material. This material responded positively to phosphotungstic acid, which was used for detection of cell wall polysaccharides. The cell wall thickness within the bulging domain was significantly lower than in other parts of trichoblasts. We suggest that internalization of cell wall polysaccharides occurs within the bulging area, contributing to local thinning of the cell wall and providing a source of osmotically active compounds for maintaining turgor in the trichoblast. Thus, the internalization process might be necessary for root hair outgrowth.

THE ELECTRON MICROSCOPY OF LEAF SURFACES PRESERVED IN PEAT

1966 ◽  
Vol 44 (4) ◽  
pp. 421-427 ◽  
Author(s):  
John M. Stewart ◽  
Edward A. C. Follett
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Calluna Vulgaris ◽  
Surface Features ◽  
Peat Deposits ◽  
Leaf Surfaces ◽  
Definition Of ◽  
Peat Formation ◽  
Physical And Chemical ◽  
Cuticular Surface

Phragmites communis, Eriophorum vaginatum, Calluna vulgaris, and Sphagnum palustre are representative of plants whose remains are frequently encountered in Scottish peat deposits. The effects of preservation in peat on the surface features of their leaves were followed by electron microscopy. Wax projections were observed on the surfaces of mature living leaves of Phragmites and Eriophorum but not on Calluna or Sphagnum. Details of cell wall outlines and stomata (or pores) were clearly defined in Phragmites, Eriophorum, and Sphagnum, but obscured in Calluna. The previous year's leaves differed by displaying a general absence of wax projections, an erosion of the cuticular surface, which took the form of either a loss in definition of the cell wall outlines or a definite etching of the surface, and the presence of numerous microorganisms. The surface features of preserved leaves exhibited to a greater degree this erosion of cell wall outline and cuticular surface. This preliminary study has indicated that major alterations in the submicroscopic features of cuticularized leaf surfaces occur at the leaf litter stage. The primary agents responsible for this degradation would appear to be microorganisms in conjunction with the physical and chemical processes of peat formation.

Postjunctional supersensitivity of the rat vas deferens and gap junctions

1976 ◽  
Vol 54 (3) ◽  
pp. 412-416 ◽  
Author(s):  
D. M. Paton ◽  
J. Buckland-Nicks ◽  
A. Johns
Keyword(s):  
Electron Microscopy ◽  
Gap Junctions ◽  
Spontaneous Activity ◽  
Vas Deferens ◽  
Rat Vas Deferens ◽  
Sprague Dawley ◽  
Glutaraldehyde Fixation ◽  
Sprague Dawley Rats

Tissues from the duodenum and vas deferens of Sprague–Dawley rats were examined of the rat vas deferens and gap junctions. Can. J. Physiol. Pharmacol. 54, 412–416. by electron microscopy after glutaraldehyde fixation and postosmication. Gap junctions (nexuses) were readily demonstrated in the duodenum in both control and reserpine treated animals (1.0 mg/kg per day for 7 days). However, gap junctions could not be demonstrated in vas deferens. It is concluded that the postjunctional supersensitivity and spontaneous activity induced by reserpine in vas deferens, does not result from the formation of gap junctions.

Electron microscopy of the replicative events of A25 bacteriophages in group A streptococci

1972 ◽  
Vol 18 (1) ◽  
pp. 93-96 ◽  
Author(s):  
S. E. Read ◽  
R. W. Reed
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Electron Microscope ◽  
Nucleic Acid ◽  
Group A Streptococcus ◽  
Group A Streptococci ◽  
Virulent Phage ◽  
Acid Pool ◽  
Group A ◽  
A Cell

The replicative events of a virulent phage (A25) infection of a group A Streptococcus (T253) were studied using the electron microscope. The first intracellular evidence of phage replication in a cell occurred 30 min after infection with arrest of cell division and increase in the nucleic acid pool. Phage heads were evident in the nucleic acid pool of the cells 45 min after infection. Release of phages occurred by splitting of the cell wall along discrete lines. This appeared to be at sites of active wall synthesis, i.e., near the region of septum formation. Many phage components were released but relatively few complete phages indicating a relatively inefficient replicative system.

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