scholarly journals Cell Wall Organization and the Properties of the Xylem 1. Cell Wall Organization and the Variation of Breaking Load in Tension of the Xylem in Conifer Stems

1951 ◽  
Vol 4 (4) ◽  
pp. 391 ◽  
Author(s):  
ABW Ardrop
Keyword(s):  
Cell Wall ◽  
Basic Density ◽  
Breaking Load ◽  
Cellulose Content ◽  
Micellar System ◽  
Growth Rings ◽  
Cell Axis ◽  
Tracheid Length ◽  
Cell Wall Organization ◽  
Longitudinal Cell

The variation of breaking load in tension of tangential longitudinal sections of wood, taken from successive growth rings of each of six conifer stems, has been studied. An increase in this property was observed in successive growth rings from the stem centre of each specimen. This was paralleled by an increase in tracheid length, basic density, and cellulose content. The inclination to the longitudinal cell axis of the spiral micellar system of the cell wall decreased with increasing tracheid length.

scholarly journals The Cell Wall Structure of Xylem Parenchyma

1952 ◽  
Vol 5 (2) ◽  
pp. 223 ◽  
Author(s):  
AB Wardrop ◽  
HE Dadswell
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Secondary Cell Wall ◽  
Primary Cell Wall ◽  
Wall Structure ◽  
Xylem Parenchyma ◽  
Cell Axis ◽  
X Ray ◽  
Ray Methods ◽  
Longitudinal Cell

The fine structure of the cell wall of both ray and vertical parenchyma has been investigated. In all species examined secondary thickening had occurred. In the primary cell wall the micellar orientation was approximately trans"erse to the longitudiJ)aI cell axis. Using optical and X-ray methods the secondary cell wall was shown to possess a helical micellar organization, the micelles being inclined between 30� and 60� to the longitudinal cell axis.

scholarly journals The Nature of Reaction Wood II. The Cell Wall Organization of Compression Wood Tracheids

1950 ◽  
Vol 3 (1) ◽  
pp. 1 ◽  
Author(s):  
AB Wardrop ◽  
HE Dadswell
Keyword(s):  
Cell Wall ◽  
Pinus Radiata ◽  
Compression Wood ◽  
Large Angle ◽  
Reaction Wood ◽  
Micellar Structure ◽  
X Ray ◽  
Similar Length ◽  
Tracheid Length ◽  
Cell Wall Organization

Optical and X-ray methQds have been used in the examinatiQn Qf the secQndarycell wall Qf cQmpressiQn WQQd tracheids from a number Qf species QfgymnDsperms.By these methQds it has been shQwn that the cell wall Qf CQmpressiQn WQQd tracheidscDnsists Qf two. layers. In the Quter layer the micelles are inclined at a large angle 'to. the lQngitudinal axis Qf the tracheid, while in the inner layer the micelles areinclined at a relatively smaller angle. In the inner Df the two. layers there exist radialdiscQntinuities in the spiral micellar structure, which are visible as IQngitudinal striatiQnsin the cell wall. These discQntinuities also. aCCQunt for the radial distributiQn Qflignin which is observed in transverse sectiQns Qf cQmpressiQn WQQd tracheids. Bydetermining the average tracheid length Qf the last-fDrmed late WQod in the variQusgrowth rings Df several eccentric stems Qf Pinus radiata D.DQn it has been shDwn thatthe tracheids Qf cQmpressiQn WQQd are appreciably shQrter than WQuld be the case ifno. cQmpressiQn WQQd were present. A study Qf the change in micellar QrientatiQn withchange in tracheid length has indicated that the angle Qf micellar QrientatiQn in CQmpressiQnWQQd tracheids dQes nQt differ signific(mtly frQm that existing in nQrmalWQQd tracheids Qf similar length. In so. far as the prQperties Qf WQQd are determinedby cell wall QrganizatiQn, it is cQncluded that cQmparisQns between cQmpressiQn WQDdand normal WQQd shQuld be made Qn material Qf the same tracheid length and spiralQrganizatiDn. It is suggested that bQth the reductiQn in tracheid length and eccentricradial growth in stems cQntaining cQmpressiQn WQQd are to. be attributed to. an increasein the number Df bDth transverse and tangential lQngitudinal divisiQns Qf thefusifQrm initials Qf the cambium.

scholarly journals Functional Characterisation of the Poplar Atypical Aspartic Protease Gene PtAP66 in Wood Secondary Cell Wall Deposition

Forests ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1002
Author(s):  
Shenquan Cao ◽  
Cong Wang ◽  
Huanhuan Ji ◽  
Mengjie Guo ◽  
Jiyao Cheng ◽  
...  
Keyword(s):  
Cell Wall ◽  
Secondary Cell Wall ◽  
Fluorescent Protein ◽  
Secondary Xylem ◽  
Populus Trichocarpa ◽  
Wood Formation ◽  
Protease Gene ◽  
Cellulose Content ◽  
Transcription Analysis ◽  
Functional Characterisation

Secondary cell wall (SCW) deposition is an important process during wood formation. Although aspartic proteases (APs) have been reported to have regulatory roles in herbaceous plants, the involvement of atypical APs in SCW deposition in trees has not been reported. In this study, we characterised the Populus trichocarpa atypical AP gene PtAP66, which is involved in wood SCW deposition. Transcriptome data from the AspWood resource showed that in the secondary xylem of P. trichocarpa, PtAP66 transcripts increased from the vascular cambium to the xylem cell expansion region and maintained high levels in the SCW formation region. Fluorescent signals from transgenic Arabidopsis plant roots and transiently transformed P. trichocarpa leaf protoplasts strongly suggested that the PtAP66-fused fluorescent protein (PtAP66-GFP or PtAP66-YFP) localised in the plasma membrane. Compared with the wild-type plants, the Cas9/gRNA-induced PtAP66 mutants exhibited reduced SCW thickness of secondary xylem fibres, as suggested by the scanning electron microscopy (SEM) data. In addition, wood composition assays revealed that the cellulose content in the mutants decreased by 4.90–5.57%. Transcription analysis further showed that a loss of PtAP66 downregulated the expression of several SCW synthesis-related genes, including cellulose and hemicellulose synthesis enzyme-encoding genes. Altogether, these findings indicate that atypical PtAP66 plays an important role in SCW deposition during wood formation.

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.

Distribution of juvenile wood in two stems of Larixlaricina

1986 ◽  
Vol 16 (5) ◽  
pp. 1041-1049 ◽  
Author(s):  
K. C. Yang ◽  
C. A. Benson ◽  
J. K. Wong
Keyword(s):  
Juvenile Wood ◽  
Growth Ring ◽  
Ring Width ◽  
Tree Level ◽  
Growth Rings ◽  
Vertical Variation ◽  
Strong Negative Correlation ◽  
Ring Number ◽  
Tracheid Length ◽  
Growth Ring Width

The distribution and vertical variation of juvenile wood was studied in an 81-year-old dominant tree and an 83-year-old suppressed tree of Larixlaricina (Du Roi) K. Koch. Two criteria, growth ring width and tracheid length, were used to demarcate the boundary of juvenile wood. The width of juvenile wood, expressed in centimetres and the number of growth rings, decreased noticeably from the base to the top of the tree. The volume of juvenile wood decreased in a similar pattern. These decreasing trends had a strong negative correlation with the year of formation of cambial initials at a given tree level. The length of these cambial initials decreased with increasing age of formation of the cambial initials. In the juvenile wood zone, there was a positive linear regression between the growth ring number (age) and the tracheid length. The slopes of these regression lines at various tree levels increased as the age of the year of formation of the cambial initials increased. At a given tree level, the length of tracheids increased from the pith to a more uniform length near the bark. However, the number of years needed to attain a more uniform tracheid length decreased from the base to the top of the tree. These relationships suggest that the formation of juvenile wood is related to the year of formation of the cambial initials. Consequently, the juvenile wood is conical in shape, tapering towards the tree top.

scholarly journals Comparative transcriptomics indicate changes in cell wall organization and stress response in seedlings during spaceflight

2017 ◽  
Vol 104 (8) ◽  
pp. 1219-1231 ◽  
Author(s):  
Christina M. Johnson ◽  
Aswati Subramanian ◽  
Sivakumar Pattathil ◽  
Melanie J. Correll ◽  
John Z. Kiss
Keyword(s):  
Cell Wall ◽  
Stress Response ◽  
Comparative Transcriptomics ◽  
Cell Wall Organization

scholarly journals Cellulose synthase interactive1- and microtubule-dependent cell wall architecture is required for acid growth in Arabidopsis hypocotyls

2020 ◽  
Vol 71 (10) ◽  
pp. 2982-2994 ◽  
Author(s):  
Xiaoran Xin ◽  
Lei Lei ◽  
Yunzhen Zheng ◽  
Tian Zhang ◽  
Sai Venkatesh Pingali ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Elongation ◽  
Plant Cell Wall ◽  
Cellulose Microfibrils ◽  
Crystalline Cellulose ◽  
Cellulose Content ◽  
Acid Growth ◽  
Cell Wall Assembly ◽  
Dependent Cell ◽  
Cell Wall Architecture

Abstract Auxin-induced cell elongation relies in part on the acidification of the cell wall, a process known as acid growth that presumably triggers expansin-mediated wall loosening via altered interactions between cellulose microfibrils. Cellulose microfibrils are a major determinant for anisotropic growth and they provide the scaffold for cell wall assembly. Little is known about how acid growth depends on cell wall architecture. To explore the relationship between acid growth-mediated cell elongation and plant cell wall architecture, two mutants (jia1-1 and csi1-3) that are defective in cellulose biosynthesis and cellulose microfibril organization were analyzed. The study revealed that cell elongation is dependent on CSI1-mediated cell wall architecture but not on the overall crystalline cellulose content. We observed a correlation between loss of crossed-polylamellate walls and loss of auxin- and fusicoccin-induced cell growth in csi1-3. Furthermore, induced loss of crossed-polylamellate walls via disruption of cortical microtubules mimics the effect of csi1 in acid growth. We hypothesize that CSI1- and microtubule-dependent crossed-polylamellate walls are required for acid growth in Arabidopsis hypocotyls.

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