scholarly journals Changes in anatomical structure of apple fruitlet pedicels preceding June drop

2013 ◽  
Vol 35 (1) ◽  
pp. 11-23 ◽  
Author(s):  
Hanna Habdas ◽  
Leszek S. Jankiewicz ◽  
Bożena Borkowska
Keyword(s):  
Anatomical Structure ◽  
Xylem Parenchyma ◽  
Phloem Tissue ◽  
Xylem Development ◽  
Parenchyma Cells ◽  
Phloem Fibers ◽  
June Drop

The anatomical structure of pedicels of apple fruitlets was investigated. The fruitlets of cv. 'Mcintosh' and 'Bancroft' were collected on June 8th, 16th an 24th. The middle date coincided with the beginning of June drop. The pedicel structure of larger fruitlets which tended to be retained on the tree was compared with that of smaller fruitlets which tended to be shed of. In the pedicels of larger fruitlets, development of the xylem, especially secondary one, was more intensive. This difference increased in time. Lignification of cortex sclereids, phloem fibers, xylem parenchyma cells and pith cells was also more advanced. The differences in the amount of phloem tissue between both kinds of fruitlets were not large but usually significant. The mentioned differences especially in pedicel xylem development are considered to be partly responsible for the fact that smaller fruitlets loose gradually their ability to compete for nutrients. This finally leads to their starvation and shedding.

Elemental Analysis of Phloem Tissue in Lemna Minor Root Tips

1980 ◽  
Vol 38 ◽  
pp. 798-799
Author(s):  
Patrick Echlin ◽  
Thomas Hayes ◽  
Clifford Lai ◽  
Greg Hook
Keyword(s):  
Vascular Tissue ◽  
Lemna Minor ◽  
Atomic Weight ◽  
Companion Cell ◽  
Root Tips ◽  
Phloem Tissue ◽  
Cell Stage ◽  
Phloem Parenchyma ◽  
Parenchyma Cells ◽  
Xylem Element

Studies (1—4) have shown that it is possible to distinguish different stages of phloem tissue differentiation in the developing roots of Lemna minor by examination in the transmission, scanning, and optical microscopes. A disorganized meristem, immediately behind the root-cap, gives rise to the vascular tissue, which consists of single central xylem element surrounded by a ring of phloem parenchyma cells. This ring of cells is first seen at the 4-5 cell stage, but increases to as many as 11 cells by repeated radial anticlinal divisions. At some point, usually at or shortly after the 8 cell stage, two phloem parenchyma cells located opposite each other on the ring of cells, undergo an unsynchronized, periclinal division to give rise to the sieve element and companion cell. Because of the limited number of cells involved, this developmental sequence offers a relatively simple system in which some of the factors underlying cell division and differentiation may be investigated, including the distribution of diffusible low atomic weight elements within individual cells of the phloem tissue.

Silica in Woody Stems

1974 ◽  
Vol 22 (2) ◽  
pp. 211 ◽  
Author(s):  
G Scurfield ◽  
CA Anderson ◽  
ER Segnit
Keyword(s):  
The Other ◽  
X Ray Diffraction ◽  
Xylem Parenchyma ◽  
X Ray ◽  
Woody Perennial ◽  
Internal Surfaces ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells ◽  
Scanning Electron

Scanning electron microscopy has been used to examine silica isolated by chemical means from the wood of 32 species of woody perennial. The silica consists of aggregate grains lying free in the lumina or in ray and xylem parenchyma cells in 24 of the species. It occurs as dense silica in the other species, filling the lumina or lining the internal surfaces of vessels (and fibres) in all cases except Gynotroches axillaris where it is deposited in ray parenchyma cells. Infrared spectra and X-ray diffraction diagrams, obtained for specimens of both sorts of silica, are indistinguishable from those for amorphous silica. Aggregate grain and dense silicas are also alike in that their differential thermal analysis curves show a rather broad endothermic peak between 175° and 205°C. The results are discussed in relation to possible modes of deposition of the two sorts of silica and the tendency for silica in ray parenchyma cells to be associated with polyphenols.

Presence of supercooling-facilitating (anti-ice nucleation) hydrolyzable tannins in deep supercooling xylem parenchyma cells in Cercidiphyllum japonicum

Planta ◽  
2011 ◽  
Vol 235 (4) ◽  
pp. 747-759 ◽  
Author(s):  
Donghui Wang ◽  
Jun Kasuga ◽  
Chikako Kuwabara ◽  
Keita Endoh ◽  
Yukiharu Fukushi ◽  
...  
Keyword(s):  
Ice Nucleation ◽  
Xylem Parenchyma ◽  
Hydrolyzable Tannins ◽  
Cercidiphyllum Japonicum ◽  
Parenchyma Cells ◽  
Deep Supercooling

scholarly journals Sucrose (JrSUT1) and hexose (JrHT1 and JrHT2) transporters in walnut xylem parenchyma cells: their potential role in early events of growth resumption

2008 ◽  
Vol 28 (2) ◽  
pp. 215-224 ◽  
Author(s):  
M. Decourteix ◽  
G. Alves ◽  
M. Bonhomme ◽  
M. Peuch ◽  
K. B. Baaziz ◽  
...  
Keyword(s):  
Potential Role ◽  
Xylem Parenchyma ◽  
Parenchyma Cells

The Protective Layer as an Extension of the Apoplast

IAWA Journal ◽  
1993 ◽  
Vol 14 (2) ◽  
pp. 163-171 ◽  
Author(s):  
J. R. Barnett ◽  
P. Cooper ◽  
Lynda J. Bonner
Keyword(s):  
Cell Wall ◽  
Protective Layer ◽  
Xylem Parenchyma ◽  
Pit Membrane ◽  
Parenchyma Cells ◽  
Deep Supercooling ◽  
Dying Cells ◽  
Tylose Formation ◽  
Universal Application

The protective layer between the cell wall and plasmalemma of xylem parenchyma cells has variously been suggested to be involved in protection of the protoplast from attack by autolytic enzymes from neighbouring, dying cells, tylose formation, deep supercooling of xylem, and strengthening of the pit. None of these ideas has universal application to all species in which parenchyma cells possess a protective layer. It is proposed instead, that the protective layer is primarily laid down in order to preserve apoplastic continuity around the protoplast of a lignified cell, bringing the entire plasmalemma surface, and not just that part of it in contact with the porous pit membrane, into contact with the apoplast. If this is so, then other functions may be coincidental, or have arisen secondarily.

NITROGEN IN WOOD AND ITS ROLE IN WOOD DETERIORATION

1966 ◽  
Vol 44 (11) ◽  
pp. 1539-1554 ◽  
Author(s):  
Ellis B. Cowling ◽  
William Merrill
Keyword(s):  
Cell Wall ◽  
Continuous Process ◽  
Wood Fiber ◽  
Significant Loss ◽  
Chemical Form ◽  
Present Knowledge ◽  
Xylem Parenchyma ◽  
Fiber Cells ◽  
Parenchyma Cells ◽  
Wood Deterioration

Based on present knowledge of the origin, amounts, chemical form, and distribution of nitrogen (N) in wood, hypotheses are proposed to explain radial gradients in N content that exist across the xylem cylinder of tree stems: (1) N in the cytoplasm of developing wood cells is diluted by apposition of cell wall substances; (2) after maturation of wood fiber cells, N in their cytoplasm is removed by elution into the transpiration stream; (3) death of xylem parenchyma cells during aging of sapwood and formation of heartwood is accompanied by removal of much of the N in their cytoplasm. Hypotheses 2 and 3 above suggest strongly that trees possess an internal recycling mechanism for conservation and reuse of the N in the cytoplasm of xylary cells.Although the supply of N in wood is meager, wood-destroying fungi readily metabolize the carbon-rich constituents of wood and produce large fruiting structures that release vast numbers of spores in nature. To account for these capacities, we postulate that these fungi employ one or more of the following three mechanisms: (1) preferential allocation of N obtainable from wood to substances and pathways highly efficient in the use of wood constituents; (2) reuse of N obtainable from wood by a dynamic and continuous process of autolysis and reuse without significant loss of N; (3) utilization of N sources outside the wood itself, for example, by fixation of atmospheric N.

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