The fine structure of the pits of Eucalyptus regnans (F. Muell.) and their relation to the movement of liquids into the wood

1960 ◽  
Vol 8 (1) ◽  
pp. 51 ◽  
Author(s):  
J Cronshaw
Keyword(s):  
Secondary Wall ◽  
Structural Features ◽  
Cellulose Microfibrils ◽  
Primary Wall ◽  
Detailed Structure ◽  
Eucalyptus Regnans ◽  
Pit Membrane ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

Observstion in the electron microscope of carbon replicas of the pits of vessels, ray parenchyma cells, fibres, and tracheids of Eucalyptus regnans has shown the detailed structure of the pit borders and the pit closing membranes. In all cases in the mature wood the primary wall is left apparently without modification as the pit membrane. Unlike the borders of the pits of fibre tracheids and tracheids, the pit borders of the vessels are not separate; the cellulose microfibrils of a border may be common to several pits. The pit borders of fibre traoheids and tracheids are developed as separate entities and have a structure similar to the pit borders of softwood tracheids. The structure of the secondary wall layers associated with the pits is described and related to the structure of the pits. The fine structural features of the pits, especially of the pit closing membranes, are discussed in relation to the movement of liquids into wood.

scholarly journals Arrangement of Cellulose Microfibrils in Walls of Elongating Parenchyma Cells

1958 ◽  
Vol 4 (4) ◽  
pp. 377-382 ◽  
Author(s):  
G. Setterfield ◽  
S. T. Bayley
Keyword(s):  
Cell Walls ◽  
Secondary Wall ◽  
Cellular Differentiation ◽  
Cellulose Microfibrils ◽  
Field Region ◽  
Primary Wall ◽  
Parenchyma Cells ◽  
Pit Field ◽  
Wall Growth ◽  
Electron Microscopes

The arrangement of cellulose microfibrils in walls of elongating parenchyma cells of Avena coleoptiles, onion roots, and celery petioles was studied in polarizing and electron microscopes by examining whole cell walls and sections. Walls of these cells consist firstly of regions containing the primary pit fields and composed of microfibrils oriented predominantly transversely. The transverse microfibrils show a progressive disorientation from the inside to the outside of the wall which is consistent with the multinet model of wall growth. Between the pit-field regions and running the length of the cells are ribs composed of longitudinally oriented microfibrils. Two types of rib have been found at all stages of cell elongation. In some regions, the wall appears to consist entirely of longitudinal microfibrils so that the rib forms an integral part of the wall. At the edges of such ribs the microfibrils can be seen to change direction from longitudinal in the rib to transverse in the pit-field region. Often, however, the rib appears to consist of an extra separate layer of longitudinal microfibrils outside a continuous wall of transverse microfibrils. These ribs are quite distinct from secondary wall, which consists of longitudinal microfibrils deposited within the primary wall after elongation has ceased. It is evident that the arrangement of cellulose microfibrils in a primary wall can be complex and is probably an expression of specific cellular differentiation.

Lignification of ray parenchyma cells in the xylem of Pinus densiflora. Part I: Microscopic investigation by POM, UV microscopy, and TOF-SIMS

Holzforschung ◽  
2014 ◽  
Vol 68 (8) ◽  
pp. 897-905 ◽  
Author(s):  
Peiming Zheng ◽  
Dan Aoki ◽  
Masato Yoshida ◽  
Yasuyuki Matsushita ◽  
Takanori Imai ◽  
...  
Keyword(s):  
Secondary Wall ◽  
Secondary Ion Mass Spectrometry ◽  
Pinus Densiflora ◽  
Lignin Content ◽  
Microscopic Investigation ◽  
Acetyl Bromide ◽  
Tof Sims ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

Abstract The lignification process from sapwood (sW) to heartwood (hW) in ray parenchyma cells (Pray) of Pinus densiflora has been analyzed by means of ultraviolet (UV) microscopy, acetyl bromide (CH3COBr) lignin determination, and time-of-flight secondary ion mass spectrometry (TOF-SIMS). The cell wall layers were localized by polarized optical microscopy (POM). POM revealed that Pray have almost no secondary wall in sW and have only the outer layer of secondary wall (S1) in the transition zone (TZ) and hW. UV microscopic observations indicated that the secondary wall of Pray, which is in contact with ray tracheids (Trray), begins to lignify in sW, while the secondary wall of Pray, which is not in contact with Trray, is partially lignified in the TZ. The secondary wall of both types of Pray is completely lignified in hW. The CH3COBr lignin content in sW is slightly lower than that in hW. In the TOF-SIMS measurements, the relative intensities of the secondary ions of guaiacyl-lignin (G-lignin) in the rays in sW are significantly lower than those in hW.

Ray Structure Differences between Rootwood and Stemwood in a Range of Softwood Species

IAWA Journal ◽  
2009 ◽  
Vol 30 (1) ◽  
pp. 71-80 ◽  
Author(s):  
Pat Denne ◽  
Siân Turner
Keyword(s):  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Structural Differences ◽  
Ray Parenchyma Cells ◽  
Practical Implications ◽  
Softwood Species

Differences between the ray structure of rootwood and stemwood were analysed in 11 species from 5 families of gymnosperms. Rootwood was consistently found to have fewer ray tracheids, with ray parenchyma cells which were taller axially, wider tangentially, but shorter radially, and had more pits per cross-field than stemwood. A scale for quantifying types of cross-field pitting is proposed, and statistically significant differences in type and diameter of cross-field pitting were found between rootwood and stemwood of most species sampled. These structural differences have practical implications for identification of gymnosperm roots, and for distinguishing between rootwood and stemwood.

Ray Structure in Root- and Stem-Wood of Larix Decidua: Implications for Root Identification and Function

IAWA Journal ◽  
2008 ◽  
Vol 29 (1) ◽  
pp. 17-23 ◽  
Author(s):  
Pat Denne ◽  
Peter Gasson
Keyword(s):  
Wood Anatomy ◽  
Larix Decidua ◽  
Stem Wood ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells ◽  
And Function

Differences in ray structure between root- and stem-wood of softwoods can cause confusion in identifying roots using keys based on stem-wood anatomy. Comparison of root- and stem-wood rays of Larix decidua showed root-wood had fewer ray tracheids, taller, wider but shorter ray parenchyma cells, and larger cross-field pits than stem-wood. The implications of these differences are considered in relation to the identification and function of roots.

INHIBITION OF WATER CONDUCTIVITY CAUSED BY WATERMARK DISEASE IN SALIX SACHALINENSIS

IAWA Journal ◽  
2000 ◽  
Vol 21 (1) ◽  
pp. 49-60 ◽  
Author(s):  
Yasuaki Sakamoto ◽  
Yuzou Sano
Keyword(s):  
Wood Anatomy ◽  
High Moisture ◽  
Water Conductivity ◽  
X Ray ◽  
Salix Sachalinensis ◽  
Water Conduction ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
High Moisture Level ◽  
Ray Parenchyma Cells

Water conduction and wood anatomy of Salix sachalinensis attacked by watermark disease were investigated. The internal symptom, the watermark, appeared as a brown to brown-black stained zone in sapwood. Dye injection tests revealed that water conduction did not take place in the watermark. However, soft X-ray photography and cryo-scanning electron microscopy revealed that the watermark had a high moisture level. In the watermark, some of the vessels were plugged with tyloses and masses of bacteria, and some of the ray parenchyma cells caused necrosis. Hence, the non-conductive watermark in sapwood can be considered similar to discoloured wood or wetwood.

Localisation structurale et ultrastructurale d'activités peroxydasiques dans les parois du mésophylle et des fibres en cours de lignification chez l'alfa (Stipa tenacissima)

1984 ◽  
Vol 62 (12) ◽  
pp. 2644-2649 ◽  
Author(s):  
M. Harche
Keyword(s):  
Peroxidase Activity ◽  
Oxidase Activity ◽  
Cell Walls ◽  
Secondary Wall ◽  
Outer Part ◽  
Potassium Cyanide ◽  
Primary Wall ◽  
Stipa Tenacissima ◽  
Parenchyma Cells

Using diaminobenzidine as substrate, peroxidase activity was localized in the walls of parenchyma cells and differentiating fibres. In mature fibres and parenchyma a slight activity could be recognized in primary walls only. In parenchyma cells, peroxidase activity was fairly inhibited with heat, potassium cyanide, and aminotriazole, which could indicate the presence of catalase within the cell walls. However, in plasmodesmatal regions peroxidases were- resistant to the above inhibitors. Syringaldazine oxidase activity was present only in the primary wall and the outer part of the secondary wall of differentiating fibres. The parallelism between lignification and peroxidase activity in the secondary walls supports the hypothesis of the involvement of these enzymes in the lignification process.

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.

Survival rate and nuclear irregularity index of sapwood ray parenchyma cells in four tree species

1993 ◽  
Vol 23 (4) ◽  
pp. 673-679 ◽  
Author(s):  
K.C. Yang
Keyword(s):  
Survival Rate ◽  
Growth Ring ◽  
Initiation Time ◽  
Heartwood Formation ◽  
Sharp Decline ◽  
Irregularity Index ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells ◽  
Marginal Cells

Survival rate and the newly developed nuclear irregularity index (NII) of sapwood ray parenchyma cells were studied within single trees of four species: Pinusbanksiana Lamb., Piceamariana (Mill.) B.S.P., Abiesbalsamea (L.) Mill., and Populustremuloides Michx. The survival rate of ray parenchyma cells is defined as the number of living earlywood ray parenchyma cells in uniseriate rays, divided by the total number of dead and living ray parenchyma cells recorded, multiplied by 100. NII is defined as the ratio of the number of irregularly shaped nuclei of uniseriate ray parenchyma cells to the total number of the irregular and regular nuclei recorded in earlywood, multiplied by 100. The location where death of ray parenchyma cells was first seen in the sapwood varied with species from the second to the seventh growth ring, counted from the cambium. In general, the marginal cells in the outer sapwood died earlier in a given growth ring than the central cells. The survival rate of the sapwood ray parenchyma cells decreased curvilinearly from the outer or middle sapwood towards the boundary of sapwood and heartwood. Based on survival rate classification, Pinusbanksiana and Populustremuloides are type II species, in which some ray parenchyma cells die in the middle or inner sapwood and the number of dead cells increases from the middle sapwood towards the heartwood. Piceamariana and Abiesbalsamea are type III species, in which some ray parenchyma cells die in outer sapwood and the number of dead cells increases from the outer sapwood towards the heartwood. NII increased from the middle of the sapwood towards the sapwood–heartwood boundary and reached its maximum at the growth ring immediately adjacent to the heartwood. NII increased from May to a maximum in the middle of the growing season and then decreased sharply. The months of sharpest decline of the NII in Pinusbanksiana, Piceamariana, and Populustremuloides were August, July–August, and August–October, respectively. In Abiesbalsamea no sharp decline of NII was observed. The findings of this study are in agreement with those of other investigators who used different criteria to indicate the initiation time of heartwood formation. Thus it appears that NII can be added to the list of indicators that pinpoint the initiation time of heartwood formation.

Wood Anatomy of Bhesa Sinica (Celastraceae)

IAWA Journal ◽  
1990 ◽  
Vol 11 (1) ◽  
pp. 57-60 ◽  
Author(s):  
Zhang Xinying ◽  
Pieter Baas ◽  
Alberta M. W. Mennega
Keyword(s):  
Wood Anatomy ◽  
The Other ◽  
Anatomical Character ◽  
The Family ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

The wood anatomy of Bhesa sinica (Chang ' Liang) Chang ' Liang, the only species of the genus occurring in China, is described in detail and compared with other Celastraceae. Bhesa sinica closely resembles other species of the genus, in e. g. vessels mainly in radial multiples, exclusively scalariform perforations, large and (almost) simple vessel-ray pits; parenchyma in fine irregular bands, in long (over 8-celled) strands; thick-walled, non septate libriform fibres; 1-5-seriate heterocellular rays, and prismatic crystals in chambered axial and ray parenchyma cells. This combination of characters is not known to occur in any of the other genera of the Celastraceae, and most individual wood anatomical character states of Bhesa are also unusual within the family. The isolated position of the genus in the Celastraceae is discussed.

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