scholarly journals Histological changes associated with the graft union development in tomato

2020 ◽  
Author(s):  
Carlos Frey ◽  
José Luis Acebes ◽  
Antonio Encina ◽  
Rafael Álvarez
Keyword(s):  
Cell Walls ◽  
Adventitious Roots ◽  
Structural Changes ◽  
Vascular Tissue ◽  
Graft Union ◽  
Vascular Connection ◽  
Horticultural Crops ◽  
Undifferentiated Cells ◽  
Long Time ◽  
Vascular Connections

Abstract Background. Despite the importance of grafting in agriculture, particularly in horticultural crops such as tomato (Solanum lycopersicum L.), the structural changes that occur during the establishment of a graft are little understood. Using histochemical techniques, the present work examines the progression of the structure of the graft junction in tomato plants over time.Results. At 10 days after grafting, the cell walls of the scion and rootstock in the area of the graft junction were thicker than usual, and undifferentiated cells appeared associated with the pre-existing vascular tissue. New vascular tissue appeared as branches arising from the pre-existing vasculature, as vascular pockets dispersed within the callus, and as the result of the transdifferentiation of parenchyma cells. Areas showing vascular connections between the scion and rootstock were also seen. Adventitious roots appeared on the scion, arising from the pre-existing vasculature. At 20 days, a great deal of vascular tissue was visible, along with large areas showing vascular connection. At 210 days, vestiges of the changes undergone were still visible. However, no adventitious roots persisted. Conclusions. The area of the graft junction undergoes modifications essential for adequate physiological functioning of grafted plant. The cell walls of the adhesion line change during the process. Pre-existing vasculature plays an important role in the appearance of callus tissue, new vascular cells, and adventitious roots. A long time later the tissues maintain vestiges of graft union development.

scholarly journals Histological Changes Associated with the Graft Union Development in Tomato

Plants ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 1479
Author(s):  
Carlos Frey ◽  
José Luis Acebes ◽  
Antonio Encina ◽  
Rafael Álvarez
Keyword(s):  
Cell Walls ◽  
Time Course ◽  
Structural Changes ◽  
Vascular Tissue ◽  
Wall Material ◽  
Histological Techniques ◽  
Vascular Connection ◽  
Horticultural Crops ◽  
Solanum Lycopersicum L ◽  
Undifferentiated Cells

Despite the importance of grafting in horticultural crops such as tomato (Solanum lycopersicum L.), the structural changes that occur during the graft establishment are little understood. Using histological techniques, the present work examines the time course of changes on the anatomical structure of the graft junction in functional tomato homografts and compares it to that of heterografts and non-functional grafts. No apparent differences were detected between homo- and heterografts, showing similar tissue development. At 10 days after grafting, the cell walls of the scion and rootstock in the area of the graft junction were thicker than usual. Undifferentiated cells and new vascular tissue emerged from the pre-existing vasculature. Adventitious roots appeared mainly on the scion, arising from the pre-existing vasculature. At 20 days, more pronounced vascular tissue was visible, along with large areas showing vascular connection. At 210 days, vestiges of the changes undergone in graft development were still visible. Generally, non-functional grafts presented layers of necrotic remains and deposition of cell wall material in the cut edges, impeding the suitable scion-rootstock connection. Our results show that accurate changes in pre-existing vasculature and the cell walls of the adhesion line are crucial to the development of functional grafts.

Conversaziones 1974

1975 ◽  
Vol 29 (2) ◽  
pp. 163-171
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Cell Walls ◽  
Structural Changes ◽  
Vascular Tissue ◽  
Root Systems ◽  
Plant Roots ◽  
Tracer Studies ◽  
Water Move ◽  
Intact Root

CONVERSAZIONES were held this year on 9 May and 27 June. At the first conversazione twenty-seven exhibits and two films were shown. The fine structure of plant roots in relation to transport of nutrient ions and water was demonstrated by Dr D. T. Clarkson of the A.R.C. Letcombe Laboratory, Wantage and Dr A. W. Robards of the Department of Biology, University of York. Two major pathways by which nutrients and water move radially across the cortex towards the central vascular tissue have been distinguished by the use of tracer studies of adsorption by different zones of intact root systems, microautoradiography and electron microscopy. Movement can be apoplastic through cell walls, or symplastic between cells joined by plasmodesmata. As the root ages, structural changes in the endodermis reduce movement in the former pathway but the symplast is not interrupted by the elaboration of endodermal walls because plasmodesmatal connexions remain intact. These observations help explain the contrasting extent to which different ions and water reach the shoot from young and mature parts of root systems.

Isolation and characterization of cell walls from the mesocarp of mature grape berries (Vitis vinifera)

2020 ◽  
Author(s):  
KJ Nunan ◽  
Ian Sims ◽  
A Bacic ◽  
SP Robinson ◽  
GB Fincher
Keyword(s):  
Vitis Vinifera ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Compositional Analysis ◽  
Water Soluble ◽  
Vitis Vinifera L ◽  
Nylon Mesh ◽  
Cytoplasmic Material ◽  
Isolation And Characterization ◽  
Tissue Homogenates

Cell walls have been isolated from the mesocarp of mature grape (Vitis vinifera L.) berries. Tissue homogenates were suspended in 80% (v/v) ethanol to minimise the loss of water-soluble wall components and wet-sieved on nylon mesh to remove cytoplasmic material. The cell wall fragments retained on the sieve were subsequently treated with buffered phenol at pH 7.0, to inactivate any wall-bound enzymes and to dislodge small amounts of cytoplasmic proteins that adhered to the walls. Finally, the wall preparation was washed with chloroform/methanol (1:1, v/v) to remove lipids and dried by solvent exchange. Scanning electron microscopy showed that the wall preparation was essentially free of vascular tissue and adventitious protein of cytoplasmic origin. Compositional analysis showed that the walls consisted of approximately 90% by weight of polysaccharide and less than 10% protein. The protein component of the walls was shown to be rich in arginine and hydroxyproline residues. Cellulose and polygalacturonans were the major constituents, and each accounted for 30-40% by weight of the polysaccharide component of the walls. Substantial varietal differences were observed in the relative abundance of these two polysaccharides. Xyloglucans constituted approximately 10% of the polysaccharide fraction and the remainder was made up of smaller amounts of mannans, heteroxylans, arabinans and galactans.

scholarly journals Overview of Popular Techniques of Raman Spectroscopy and Their Potential in the Study of Plant Tissues

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1537
Author(s):  
Aneta Saletnik ◽  
Bogdan Saletnik ◽  
Czesław Puchalski
Keyword(s):  
Raman Spectroscopy ◽  
Cell Walls ◽  
Structural Changes ◽  
Spatial Information ◽  
Technological Development ◽  
Analytical Techniques ◽  
High Sensitivity ◽  
Plant Tissues ◽  
Wide Range ◽  
Identification Technique

Raman spectroscopy is one of the main analytical techniques used in optical metrology. It is a vibration, marker-free technique that provides insight into the structure and composition of tissues and cells at the molecular level. Raman spectroscopy is an outstanding material identification technique. It provides spatial information of vibrations from complex biological samples which renders it a very accurate tool for the analysis of highly complex plant tissues. Raman spectra can be used as a fingerprint tool for a very wide range of compounds. Raman spectroscopy enables all the polymers that build the cell walls of plants to be tracked simultaneously; it facilitates the analysis of both the molecular composition and the molecular structure of cell walls. Due to its high sensitivity to even minute structural changes, this method is used for comparative tests. The introduction of new and improved Raman techniques by scientists as well as the constant technological development of the apparatus has resulted in an increased importance of Raman spectroscopy in the discovery and defining of tissues and the processes taking place in them.

The morphology of grain abscission in Zizania aquatica

1980 ◽  
Vol 58 (21) ◽  
pp. 2269-2273 ◽  
Author(s):  
H. B. Hanten ◽  
G. E. Ahlgren ◽  
J. B. Carlson
Keyword(s):  
Wild Rice ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Embryo Sac ◽  
Middle Lamella ◽  
Abscission Zone ◽  
Rice Grains ◽  
Zizania Aquatica ◽  
Parenchyma Cells ◽  
Anatomical Evidence

The anatomical development of the abscission zone in grains of Zizania aquatica L. was correlated with development of the embryo. The abscission zone is well developed when the embryo sac is mature. Soon after pollination, the first anatomical evidence of abscission appears as plasmolysis of the separation layer parenchyma cells. This is followed by separation of the layers by dissolution of the middle lamella and fragmentation of cell walls. Persistence of intact vascular tissue and presence of a surrounding cone-shaped mass of lignified cells may be involved in abscission of wild rice grains.

scholarly journals Modified Lignification in the Cell Walls of Cad Depressed Poplars

IAWA Journal ◽  
2007 ◽  
Vol 28 (4) ◽  
pp. 457-471 ◽  
Author(s):  
A. Yoshinaga ◽  
M. Wada ◽  
M. Fujital ◽  
B. Chabbert ◽  
G. Pilate
Keyword(s):  
Cell Walls ◽  
Structural Changes ◽  
Alkali Treatment ◽  
Cinnamyl Alcohol Dehydrogenase ◽  
Carbonyl Groups ◽  
Wood Fibers ◽  
Soluble Cell ◽  
Poplar Trees ◽  
Vessel Elements ◽  
Lignin Deposition

Ultraviolet microscopic spectrophotometry was used to investigate lignification in the secondary cell walls of wood fibers and vessel elements from either wild type or transgenic poplars with depressed activity of cinnamyl alcohol dehydrogenase (CAD). A distinct shoulder at 330 nm was characteristic of the transgenic poplar. Measurements performed after 1) a mild alkali treatment or 2) areduction with sodium borohydride indicated that this shoulder merely resulted from the occurrence of conjugated carbonyl groups in the lignin polymer rather than alkali-soluble cell wall bound phenolic aldehydes. UV absorbance ratios (A330 /A280) measured in the center of secondary walls in the differentiating xylem clearly showed that the structural changes observed in the lignin polymer of transgenic trees occurred very early during lignin deposition. This suggests that, in poplar trees with low CAD activity, cinnamaldehydes are incorporated into lignin even at the early stages of lignification.

Comparison of photosynthetic carbon reduction (Kranz) cells having different ontogenetic origins in the C4 NADP – malic enzyme grass Arundinella hirta

1990 ◽  
Vol 68 (6) ◽  
pp. 1222-1232 ◽  
Author(s):  
Nancy G. Dengler ◽  
Ronald E. Dengler ◽  
Douglas J. Grenville
Keyword(s):  
Cell Walls ◽  
Vascular Tissue ◽  
Cell Types ◽  
Bundle Sheath ◽  
Carbon Reduction ◽  
Bundle Sheath Cells ◽  
Photosynthetic Carbon ◽  
Arundinella Hirta ◽  
Photosynthetic Carbon Reduction ◽  
Sheath Cells

The C4 grass Arundinella hirta is characterized by unusual leaf blade anatomy: photosynthetic carbon reduction takes place both within the chlorenchymatous bundle sheath cells of the longitudinal veins and within longitudinal strands of "distinctive cells" that form part of the leaf mesophyll and are often completely isolated from vascular tissue. Although they are equivalent physiologically, these two cell types have different ontogenetic origins: bundle sheath cells are delimited from procambium early in leaf development, whereas distinctive cells differentiate from ground meristem at a later developmental stage. Although the two cell types share numerous cytological features (large chloroplasts with reduced grana, thick cell walls with a suberin lamella), we also found significant differences in cell lengths, length to width ratios, cell cross-sectional areas, organelle numbers per cell cross section, phenol content of the cell walls, and numbers of pit fields in the longitudinal cell walls. The size and shape of bundle sheath cells are likely a direct consequence of procambial origin. The thicker walls of bundle sheath cells (in major veins) and their greater lignification may reflect the inductive effect of cell differentiation in the proximity of sclerenchyma and vascular tissues. Differences between major and minor vein bundle sheath cells may reflect differences in the timing of initiation of procambial strands. Our analysis of cell wall characteristics has also shown the presence of numerous primary pit fields in the transverse walls between adjacent distinctive cells in a file; plasmodesmata in these pit fields form a pathway for longitudinal symplastic transport not previously known to exist.

Penetration and colonization of resistant and susceptible Apium graveolens by Fusarium oxysporum f.sp. apii race 2: callose as a structural response

1988 ◽  
Vol 66 (12) ◽  
pp. 2385-2391 ◽  
Author(s):  
C. M. Jordan ◽  
R. M. Endo ◽  
L. S. Jordan
Keyword(s):  
Fusarium Oxysporum ◽  
Host Cell ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Periodic Acid ◽  
Light And Electron Microscopy ◽  
Structural Response ◽  
Aniline Blue ◽  
Apium Graveolens ◽  
Race 2

Root apices of Apium graveolens L. resistant and susceptible to race 2 of Fusarium oxysporum f.sp. apii (R. Nels. & Sherb.) were studied at various times after inoculation, using light and electron microscopy to determine structural response(s) of the hosts during penetration and colonization by the pathogen. Penetration was intercellular and intracellular and involved mechanical and enzymatic mechanisms. At the onset of penetration, the host cell walls manifested fluorescence, induced with either aniline blue or sirofluor, at the point of penetration. The fluorescent area was more intense and larger in the resistant host. Fluorescence disappeared with time. After incubation with β-1,3 glucanase fluorescence disappeared, indicating β-1,3 polysaccharide (probably callose) presence. Callose deposits were 2 and 3 times greater in the epidermis and 4 and 9 times greater in the cortex of the resistant than in two susceptible hosts, respectively. Hyphal counts in the cortex of the resistant host were 50% fewer than in the susceptible hosts. Increased callose deposition on host cell walls was associated with reduced colonization. Callose formed in vascular tissue as the fungus colonized it. Callose detection with sirofluor was more sensitive; background fluorescence common with aniline blue without periodic acid – Schiff's reagent pretreatment was absent.

Electron-probe microanalysis of silicon in the adventitious roots and terminal internode of the culm of Zea mays

1982 ◽  
Vol 60 (10) ◽  
pp. 2024-2031 ◽  
Author(s):  
Daphne M. Bennett ◽  
A. G. Sangster
Keyword(s):  
Zea Mays ◽  
Electron Probe Microanalysis ◽  
Cell Walls ◽  
Electron Probe ◽  
Adventitious Roots ◽  
Zea Mays L ◽  
Outer Region ◽  
Background Level ◽  
Ground Tissue ◽  
Epidermal Cell Wall

The adventitious roots and terminal internode of the culm of mature, field-grown specimens of five cultivars of Zea mays L. were investigated with relation to silicon, using electron-probe microanalysis. No silicon was detected above the background level within the endodermis or any other tissues within the adventitious roots. In contrast, however, in the terminal internode silicon was present in the outermost layers of cells, the highest levels being detected in the outer epidermal wall. It was also present in the internal epidermal cell wall, as well as in the walls of underlying tissues of the outer region of the culm, in the sclerenchyma, and at a low level in the parenchyma forming the ground tissue. Thus, the culms displayed a decreasing gradient of silicon content, probably in the form of amorphous silica gel, in cell walls, proceeding from the outermost layer, the epidermis, to the centrally located ground parenchyma, a result generally consistent for all five cultivars. The results are discussed in relation to the anatomy of these tissues and their silicification.

scholarly journals Effects of Water Regime on the Structure of Roots and Stems of Durum Wheat (Triticum durum Desf.)

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Amina Labdelli ◽  
Ahmed Adda ◽  
Youcef Halis ◽  
Samira Soualem
Keyword(s):  
Durum Wheat ◽  
Water Deficit ◽  
Adventitious Roots ◽  
Structural Changes ◽  
Abiotic Factors ◽  
Anatomical Variations ◽  
Limiting Factors ◽  
Primary Xylem ◽  
Triticum Durum Desf ◽  
Response To Water

Yield improvement of durum wheat is considerably limited by the expression of environmental abiotic factors. Water deficits are one of these limiting factors. Plants develop various strategies to tolerate the effects of water deficit. Some of such mechanisms might occur in the root and stem systems. The present study aimed to investigate some anatomical traits contributing to the drought tolerance in the durum wheat. The anatomical variations of the meristem of roots and stems, as a response to water deficit, were evaluated. The results indicated that the enhancement of the intensity of water deficit was accompanied by profound structural changes in the piliferous zone of roots. Water deficit caused a significant decrease in the diameter of the newly formed adventitious roots, which can be explained by a reduction in the thickness of the cortical parenchyma, through the reduction of cell size. This action was usually a contrary effect in the principal adventitious roots. The study also showed that increasing the intensity of water deficit reduced the diameter of vessels in the primary xylem, thereby increasing the hydraulic resistance of roots and lowering the flow of sap.

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