Studies on compression wood—part VII: Distribution of lignin in normal and compression wood of tamarack [Larix laricina (Du Roi) K. Koch]

Summary The distribution of lignin has been studied in tracheids and ray cells of normal and compression wood of tamarack [Larix laricina (Du Roi) K. Koch]. The three layers in the secondary wall of normal wood tracheids are lignified to approximately the same extent, and previous evidence that the S ₃ layer should contain a higher proportion of lignin than the other regions has not been confirmed. The lignin follows closely the orientation of the cellulose microfibrils in all three layers. Compared to the tracheids, the ray cells contain a denser network of lignin in their secondary wall.Only a small proportion of the total lignin in compression wood tracheids is present in the compound middle lamella. The thick S ₁ layer is only slightly lignified; the orientation of the lignin in this region is that of the transversely oriented, lamellated microfibrils. The outer portion of S ₂ consists largely of lignin but also contains lamellae of cellulose microfibrils which probably have the same helical orientation as the microfibrils in the inner part of S ₂. The latter region, which contains the helical cavities, consists of lamellae of cellulose microfibrils which are uniformly encrusted with lignin. The ray cells in compression wood appear to be lignified to the same extent as in normal wood. Transverse sections of the cells reveal a lateral orientation of the lignin. The orientation of the cellulose microfibrils in the S ₂ layer of the first-formed springwood tracheids of compression wood is the same as in the cells which are formed later. It is suggested that for ease of reference, the outer, lignin-rich layer in compression wood tracheids be referred to as the S ₂(L) layer.

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Zusammenfassung Im Druckholz und im normalen Holz von Tamarack (Larix laricina (Du Roi) K. Koch) wurde die Verteilung des Lignins in Tracheiden und Markstrahlzellen untersucht. Die drei Schichten der Sekundärwand in den Tracheiden normalen Holzes werden in nahezu demselben Umfange lignifiziert. Frühere Feststellungen, daß die S ₃-Schicht einen höheren Ligningehalt erreicht als andere Zellwandbereiche, konnten also nicht bestätigt werden. Das Lignin folgt sehr genau der Orientierung der Cellulose-Mikrofibrillen aller drei Schichten. Im Vergleich zu den Tracheiden erfahren die Sekundärwände der Markstrahlzellen eine stärkere Ligninauskleidung.Nur ein geringer Prozentsatz des gesamten Lignins der Druckholztracheiden befindet sich in der Mittellamelle. Die dicke S ₁-Schicht ist nur wenig lignifiziert. Die Orientierung des Lignins in diesem Bereich entspricht den transversal orientierten, lamellierten Mikrofibrillen. Der äußere Teil der S ₂-Schicht enthält sehr viel Lignin, daneben aber auch Lamellen von Cellulose-Mikrofibrillen, die wahrscheinlich dieselbe spiralige Orientierung besitzen wie die Mikrofibrillen des inneren Teiles der S ₂-Schicht. Der letzterwähnte Bereich, der spiralige Kavitäten enthält, weist Lamellen von Cellulose-Mikrofibrillen auf, in welche gleichmäßig Lignin eingelagert ist. Die Markstrahlzellen des Druckholzes erscheinen ebenso stark lignifiziert wie die Markstrahlzellen des Normalholzes. Querschnitte durch diese Zellen lassen die laterale Orientierung des Lignins erkennen. Die Orientierung der Cellulose-Mikrofibrillen in der S ₂-Schicht der zuerst gebildeten Frühholztracheiden des Druckholzes ist dieselbe wie in jenen Zellen, die später ausgeformt werden. Es wird vorgeschlagen, daß zur eindeutigeren Kennzeichnung die äußere ligninreiche Schicht der Druckholztracheiden als S ₂(L)-Schicht bezeichnet wird.

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The authors wish to express their gratitude to Messrs. A. K. Bentum, D. C. Jones, and B. W. Simson for technical assistance. They are also thankful to Dr. D. A. I. Goring, McGill University, Montreal, Canada, for valuable discussions and for making available to them important, unpublished information. This investigation was supported by the United States Department of Agriculture, Forest Service, through Forest Service Research Grant No. 1, which is hereby gratefully acknowledged.     

Ultrastructure of compression wood in Ginkgo biloba

Summary Compression wood in the ancient Ginkgo biloba differs from that in most of the younger gymnosperms in the more angular outline of its tracheids, their thinner walls, and their lack of helical cavities. Both normal and compression woods of Ginkgo contain two types of tracheids, one wide, with a thin wall, and another, narrow, with a thicker wall. In all other respects the compression wood tracheids in Ginkgo are ultrastructurally similar to those in other gymnosperms. Helical cavities probably developed relatively late in the evolution of compression wood, since they are missing not only in Ginkgo but also in the Taxales and the Araucariaceae. The occurrence of compression wood in Ginkgo biloba indicates that this tissue probably has existed since the Devonean period. Very likely, the arborescent habit of the gymnosperms has always been dependent on their ability to form compression wood.This investigation was carried out under the McIntire-Stennis Program, Cooperative State Research Service. I am indebted to Mr. A. C. Day of this College and to Mr. A. Rezanowich of the Pulp and Paper Research Institute of Canada for kindly providing the scanning electron micrographs.     

Formation and structure of reaction wood in Buxus microphylla var. insularis Nakai

Summary Anatomical differences in xylem between the upper and lower sides formed in the inclined stems of Buxus microphylla with different angular displacement from the vertical were examined microscopically. B. microphylla exhibited a pronounced growth promotion on the lower side of the inclined stems. Formation of tension wood (gelatinous fibers) was not observed. Xylem formed on the lower side showed some interesting features resembling the compression wood formed in gymnosperms. The reaction wood tracheids and vessels showed an excessive lignification in their secondary walls but lacked both helical cavities and an S₃ layer, features that were almost the same as those of primitive gymnosperms. These results indicate that B. microphylla has an ability to form compression wood, suggesting that in the genus Buxus a different mechanism in the conducting elements was developed in the phylogenetic evolution.The first author would like to express his sincere thanks to Dr. T. E. Timell, College of Environmental Science and Forestry, State University of New York, Syracuse, New York, for his invaluable suggestions in connection with this research     

Distribution of lignin in normal and compression wood of Pinus taeda L.

Summary The distribution of lignin in normal and compression wood of loblolly pine (Pinus taeda L.) has been studied by the technique of lignin skeletonizing. Hydrolysis of the wood carbohydrates with hydrofluoric acid left normal wood tracheids with a uniform distribution of lignin in the S1 and S2 cell wall layers. However, the S3 region of both earlywood and latewood tracheids consistently retained a dense network of unhydrolyzable material throughout, perhaps lignin.Lignin content in compression wood averaged about 7% more than in normal wood and appears to be concentrated in the outer zone of the S2 layer. The inner S2 region, despite helical checking, is also heavily lignified. The S1 layer, although thicker than normal in compression wood tracheids, contains relatively little lignin.Ray cells, at least in normal wood, appear to be lignified to the same extent, if not more so in certain cases, than the longitudinal tracheids. Other locations where lignin may be concentrated include initial pit border regions and the membranes of bordered pits.This report is a detailed excerpt from the Ph. D. dissertation of R. A. P. Financial support provided by the College of Forestry at Syracuse University and the National Defense Education Act is hereby gratefully acknowledged.     

Significance of laricinan in compression wood tracheids

Summary After a -D-1,3-linked glucan had been isolated from compression wood, identified, and named laricinan, other researchers suggested that it occupied the helical cavities in the S₂ layer of those tracheids. They postulated that the glucan was responsible for the capacity of compression wood to generate the large forces associated with reorientation of displaced stems and branches, and also caused its severe shrinkage with drying.Analyses herein indicate that it is improbable that such a glucan could be the primary factor responsible for those characteristics of compression wood. An alternative significance is proposed, namely that its presence strengthens the already well-supported deduction that the helical cavities have a schizogenous origin.     

Arrangement of cortical microtubules in compression wood tracheids of Taxus cuspidata visualized by confocal laser microscopy

Cortical microtubules (MTs) in differentiating compression wood tracheids of Taxus cuspidata stems were visualized by confocal laser microscopy. They were oriented obliquely at an angle of about 45° to the tracheid axis during formation of the secondary wall. Artificial inclination altered the pattern of alignment of MTs. Banding MTs were helically oriented late during the formation of the secondary walls. These results indicate that MTs might control the orientation and localized deposition of cellulose microfibrils in the secondary walls of compression wood tracheids.Part of this report was presented at the 46th annual meeting of the Japan Wood Research Society, Kumamoto, April 1996     

Microfibril angle non-uniformities within normal and compression wood tracheids

The pattern and extent of variation of microfibril angle (MFA) in normal and compression tracheids of softwood were investigated by using confocal laser scanning microscopy technique. All measurements support the idea that the orientation of microfibrils in single wood tracheids is not uniform. MFA of the radial wall of earlywood tracheids was highly non-uniform and had an approximately circular form of arrangement around the bordered pits (inside the border). Between the bordered pits the measured MFAs were less than the other parts of the tracheid. In the latewood tracheids MFA was less variable. The average orientation of simple pits in the crossfield region was consistent with the mean MFA of the tracheids; however some of the measurements showed a highly variable arrangement in the areas between the simple pits. In many cases the local measured MFAs of compression wood tracheids agreed with the orientation of natural helical cavities of compression wood. Comparing the measured results in different growth rings showed that MFAs in juvenile wood are generally larger than in perfect wood.     

Studies on opposite wood in conifers part II: Histology and ultrastructure

Summary A study has been made of the histology and ultrastructure of opposite wood in Larix laricina, Picea rubens, and Pinus resinosa. The width of the growth rings varied considerably, in one case from 0.1–1.0 mm, with the wide rings containing a much higher proportion of latewood than the narrow ones. The earlywood tracheids were square in outline and more regularly arranged than in normal wood. In the latewood they were sometimes irregular and distorted. The S₃ layer in the tracheids was 0.2 m thick in the earlywood and 0.4–0.8 m in the latewood, as compared to a thickness in normal wood of 0.1–0.2 m in both zones. The S₃ was often buckled in the latewood and was terminated towards the lumen by a spiral thickening. The cell wall structure of the tracheid pit border was described. Normal coniferous wood might be regarded as an intermediate between opposite wood and compression wood.This paper is dedicated to Dean Edwin C. Jahn in honor of his 70th birthday.     

Anatomy and lignin distribution of reaction wood in two Magnolia species

Summary Anatomical features of reaction wood formed in two Magnolia species, M. obovata Thunb. and M. kobus DC. which are considered to be among the primitive angiosperms, were observed. In addition, the distribution of guaiacyl and syringyl units of lignins in the cell walls of normal and reaction wood was examined using ultraviolet (UV)- and visible light (VL)- microspectrophotometry coupled with the Wiesner and M?ule reactions. The two Magnolia species formed a tension-like reaction wood without possessing the typical gelatinous layer (G-layer) on the upper side of the inclined stem or branch, in which a radial growth promotion occurred. Compared with the normal wood, the reaction wood had the following anatomical features: (1) the secondary walls of fiber tracheids lacked the S₃ layer, (2) the innermost layer of fiber-tracheid walls showed a small microfibril angle, a fact being similar to the orientation of the microfibril angle of the G-layer in tension wood, and (3) the amounts of lignin decreased in the cell walls of fiber tracheids, especially with great decrease in proportion of guaiacyl units in lignins. In addition, VL-microspectrophotometry coupled with the Wiesner and M?ule reactions adopted in the present study showed potential to estimate the lignin contents in the cell walls and the proportion of guaiacyl and syringyl units in lignins. Received: 15 July 1998     

Heterogeneity in formation of lignin

Summary The formation of lignin in the cell wall of compression wood of Pinus thunbergii was examined by selective radio-labeling of specific structural units in the lignin and visualization of the label in the different morphological regions by microautoradiography. Deposition of lignin in the tracheid cell wall of compression wood occurred in the order: p-hydroxyphenyl, guaiacyl and syringyl lignin, which is the same order as observed in normal wood. However, the period of lignification in the compression wood was quite different from those of normal and opposite woods. The p-hydroxyphenyl units were deposited mainly in the early stage of cell wall formation in compound middle lamella in normal and opposite woods, while in compression wood, they were formed in both the compound middle lamella and the secondary wall. The most intensive lignification was observed during the formation of the S₂ layer, proceeding from the outer to inner S₂ layers for a long period in compression wood. In the normal or opposite woods, in contrast, the lignification became active after formation of S₃ had begun, then proceeded uniformly in the secondary wall and ended after a short period.A part of this report was originally presented at the 1989 International Symposium on Wood and Pulping Chemistry at Raleigh, NC, U.S.A.     

Recent progress in the chemistry and topochemistry of compression wood

Summary A review of the chemistry and topochemistry of compression wood with 200 references. Compression wood contains on the average 30% cellulose, 35–40% lignin, 10% galactan, 9% galactoglucomannan, 8% xylan, and 2% of a 1,3-glucan (laricinan). The cellulose is less crystalline, and the xylan has fewer arabinose side chains than in normal wood. The lignin is composed of guaiacylpropane and p-hydroxyphenylpropane units. It is more condensed, has a higher proportion of carbon-carbon bonds, and contains fewer arylglycerol--aryl ether structures than a normal conifer lignin. The ray cells and the primary wall of the tracheids have the same chemical composition in normal and compression woods. The galactan is largely located in the outer region of the secondary wall. Only 5–10% of the lignin in compression wood tracheids is extracellular. The middle lamella is less lignified than in normal wood, while the S₁ and inner S₂ layers have a lignin concentration of 30–40% which is twice as high as in normal wood. The lignin content of the S₂ (L) layer is equal to or higher than that of the intercellular region along the wall. The review is concluded with a brief reference to areas where present information is incomplete or lacking.A portion of an Academy Lecture of the International Academy of Wood Science, presented at the International Symposium on Wood and Pulping Chemistry (Ekmandagarna 1981), held in Stockholm, Sweden, June 9–12, 1981. Reprints of the unabridged review, published under the title Recent Progress in the Chemistry, Ultrastructure, and Formation of Compression Wood in the preprints of the symposium (SPCI Report 38, Vol. 1, p. 99–147) are available from the author. I wish to express my gratitude to my colleague Professor Robert A. Zabel for generous travel assistance     

Distribution of lignin in normal and tension wood

Summary The distribution of lignin in normal and tension wood of four hardwood species has been studied by examination in the electron microscope of the lignin skeletons remaining after removal of the polysaccharides with hydrofluoric acid. In normal wood fibers, the S₁ had a higher lignin concentration than the S₂ layer, which was not as highly lignified as in conifer tracheids. Vessels had a high concentration of lignin in both normal and tension wood, while the extent of lignification of the parenchyma was variable.In tension wood fibers, the S₁ and S₂ layers were highly lignified. A thick, unlignified G-layer was often associated with an extremely thin S₂ layer with a high concentration of lignin. In both normal and tension wood, the lignin had the same orientation as the cellulose micro-fibrils in the different cell wall layers. The results confirm the earlier conclusion that, in the species investigated, the same amount of lignin is present in gelatinous as in normal fibers. Evidently, the lignification mechanism operates normally in the non-gelatinous layers of the fibers, as well as in the vessels and in the parenchyma of tension wood.

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Zusammenfassung Die Ligninverteilung im Normalholz und im Druckholz von vier Laubhölzern wurde untersucht. Die Ligningerüste, die nach der Entfernung der Polysaccharide durch Fluorwasser-stoffsäure übrigblieben, wurden im Elektronenmikroskop beobachtet. In den Normalholzfasern hatte die S₁-eine höhere Ligninkonzentration als die S₂-Schicht, die weniger lignifiziert war als in den Koniferentracheiden. Die Gefäße hatten eine hohe Ligninkonzentration in sowohl Normal-als in Zugholz, während der Lignifizierungsgrad der Parenchymzellen variierte.In den Zugholzfasern waren die S₁- und S₂-Schichten völlig lignifiziert. Eine dicke, unlignifizierte G-Schicht war oft mit einer außerordentlich dünnen S₂-Schicht, die eine hohe Ligninkonzentration zeigte, verbunden. Sowohl im Normal- wie auch im Zugholz besaß das Lignin dieselbe Orientierung wie die Cellulosemikrofibrillen in den verschiedenen Zellwandschichten. Die Ergebnisse bestätigen den früheren Schluß, daß in den hier untersuchten Laubhölzern in den gelatinösen und in den normalen Fasern dieselbe Ligninmenge vorliegt. Offenbar läuft der Mechanismus der Lignifizierung in den S₁- und S₂-Schichten der gelatinösen Fasern des Zugholzes normal ab.

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This investigation was supported by the United States Department of Agriculture, Forest Service, through Forest Service Research Grant No. 1, which is hereby gratefully acknowledged.     

Interpretation of X-ray diffractograms of wood for assessments of microfibril angles in fibre cell walls

Summary Graphical models have been developed to represent X-ray diffraction patterns for microfibril arrangements in each of the characteristic secondary wall layers of fibres in normal earlywood, latewood, compression wood, and tension wood. Models for usual combinations of typical layers S₁, S₂, and S₃, and for complex tissues including more than one S₂ layer class indicate a basis for a new analytical technique for diffractograms.Diffractograms of tissues from earlywood or latewood zones may involve effects of three to four S₂ layer variations, possibly including tension wood or compression wood. The new technique enables assessment of the microfibril angle for each. Corresponding probable experimental errors are considered. Thus it is demonstrated that, even without direct calibration by other methods for measuring microfibril angle, realistic comparative values may be obtained for all S₂ layer classes substantially represented. Such data constitute significantly more reliable indices of actual values than those provided by other techniques. Also, the data give qualitative information on other aspects of the variability of fibre types within each specimen.     

Comparative study of anatomy and lignin distribution in normal and tension wood of Salix gordejecii

Fibre morphology, anatomy and ultrastructure in cell wall of Salix gordejecii normal wood were examined by transmission electron microscopy (TEM). S. gordejecii tension wood can be recognized anatomically by the presence of gelatinous (G) fibres, which contain a conspicuously thickened inner cell wall layer. TEM images showed that cell wall of S. gordejecii normal wood was typically divided into three layers including the primary wall (P), the middle lamellar (ML) and the secondary wall (S₁, S₂ and S₃). Lignin distribution was determined by using confocal laser scanning microscopy (CLSM) and transmission electron microscopy with energy dispersive X-ray analysis (TEM-EDXA). Confocal images (530 nm) of S. gordejecii normal wood showed strongly lignified CCML, and weakly lignified ML and S2 layer. Weakly lignified fibres (F) and strongly lignified vessels (V) were also detected by using CLSM. Results obtained from confocal microscopy were further confirmed by using TEM-EDXA, indicating that the ratio of lignin concentration in CCML, ML and S2 is 1.72 (1321):1.31 (1006):1 (768). Lignin distribution in tension wood is similar to that in normal wood, except for the non-lignified G layer.     

Helical fissures in compression wood cells: Causative factors and mechanics of development

Summary There is evidence showing that lignification causes both an increase in the thickness of the walls, and changes in the overall width or circumference of wood cells. Although data are not available on changes in length during lignification, it can be deduced that these must also tend to occur. As lignin occupies sites in the cell walls corresponding to those occupied by water, the theory of anisotropic shrinkage of wood may be used to predict the proportional dimensional changes tending to occur as each wall layer in a compression wood cell is lignified. Taking account of the microfibril angles in those layers, it is shown that if the angle for S₂ is more than about 45°, inevitably S₂ will tend to develop deep helical fissures or splits of the form of those reported in the literature.     

Lignin distribution across tracheid cell walls of poorly lignified wood from deformed copper deficient Pinus radiata (D. Don)

Summary Lignin topochemistry of tracheid walls from a deformed, copper deficient Pinus radiata (D. Don) tree was examined by linescan and point analyses using a Scanning Electron Microscope and Energy Dispersive Spectrometry. Both opposite and compression wood had abnormal lignin distributions compared to those observed in normal wood from a straight tree. Lignin contents in the compound middle lamella were lower than lignin contents in the secondary wall in both opposite and compression wood tracheids.One of us (G. D.) held a Commonwealth Forestry Postgraduate Research Award during this study. The research was supported in part by a grant from the Reserve Bank of Australia Rural Credits Development Fund, the Pine Fund, and members of the forest industry     

Certain seasonal changes in balsam fir cambium and its derivatives

Summary The seasonal cambial activity of balsam fir producing normal and compression wood was observed. Samples were taken throughout one growing season. Activity was initiated in normal wood with the precocious development of one sieve cell per file 2 weeks before activity was initiated in compression wood with the formation of one new sieve cell per file. Deactivation dates in normal and compression wood were the same.Dating of the phloem adjacent to normal wood can be carried out using crushed sieve cells or an annually formed band of tannin filled parenchyma whereas adjacent to compression wood, only crushed sieve cells can be used.The maximum cambial zone widths in normal and compression wood were 15 and 16 cells, respectively. The final xylem to phloem ratio in normal wood was 14:1 while in compression wood it was 21:1.Time required for development of tracheids was examined throughout the growing season. Growth trends for the radial growth and differentiation phases were studied in both normal and compression wood. Tracheid development in normal wood took between 14 and 33 days while in compression wood it varied between 5 and 49 days.Research financed under McIntire-Stennis Research Project 5009 and COE Projects R625-173 and R625-195     

Morphological changes in the cytoskeleton, nuclei, and vacuoles during cell death of short-lived ray tracheids in the conifer Pinus densiflora

Morphological changes in the cytoskeleton, nuclei, and vacuoles were monitored during the cell death of short-lived ray tracheids in the conifer Pinus densiflora. After formation of the dentate thickenings that occurred at the final stage of formation of cell walls, organelles started to disappear in differentiating ray tracheids. First, the microtubules and vacuoles disappeared. Then actin filaments disappeared in the differentiating ray tracheids adjacent to ray tracheids that lacked nuclei, and, finally, the nuclei disappeared. These features indicate that cell death in ray tracheids might differ from the programmed cell death of tracheary elements that has been studied in vitro in the Zinnia culture system. This study was presented at the 57th Annual Meeting of the Japan Wood Research Society, August 8–10, 2007, Hiroshima, Japan     

Radial and between-family variations of the microfibril angle and the relationships with bending properties in Picea jezoensis families

With emphasis on tree breeding for wood quality in Picea jezoensis, we aimed to evaluate radial and between-family variations in the microfibril angle (MFA) of the S₂ layer in the latewood tracheids in 10 open-pollinated families of 43-year-old P. jezoensis trees. In addition, the relationships between MFA/wood density with the modulus of elasticity (MOE) or modulus of rupture (MOR) were investigated. Significant differences in MFA between families were found from the pith toward the bark. MFA showed higher values around the pith area, although some families showed relatively lower values than others around this area. In addition, due to a larger coefficient of variations of MFA near the pith, the potential for juvenile wood MFA improvement may be greater compared with mature wood. MOE was correlated with MFA in juvenile wood and with wood density in mature wood, whereas MOR was mainly correlated with wood density at radial positions in both woods. Therefore, to improve the MOE and MOR of P. jezoensis wood, both MFA and wood density would be factors to consider in both juvenile and mature woods. On the other hand, there are indications that, only wood density would be an important criterion for improving mature wood properties.     

Fibril angle variability in earlywood of Norway spruce using soft rot cavities and polarization confocal microscopy

The main purpose of this study was to investigate the variability of the fibril angle of tracheids in earlywood of Norway spruce (Picea abies L. Karst.). Polarization confocal microscopy was chosen and compared with the method utilizing the orientation of soft rot cavities. There was a significant correlation between the soft rot and polarization confocal microscopy methods, which showed the same trend of high fibril angles in the first part of the earlywood followed by a decrease toward the end of earlywood. This declining trend was less pronounced in annual rings containing compression wood. Moreover, large variations in fibril angle occurred between neighboring tracheids. The investigation also emphasized the differences between X-ray diffraction and microscopic methods, as the large variation seen by the latter methods is not seen by the X-ray diffraction approach because of its large area of measurement. No correlation was found between fiber morphology (i.e., average length, width, density) and the average fibril angle in the investigated annual rings.