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.     

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.     

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     

Helical thickenings and helical cavities in normal and compression woods of Taxus baccata

Summary The longitudinal tracheids in compression wood of Taxus baccata contain helical thickenings but no helical cavities. The thickenings are as frequent and well developed and have the same ropelike appearance as in normal wood of this species. They are an integral part of the S₃ in normal and of the S₂ in compression wood and have the same orientation as the innermost microfibrils in these layers. Except for the absence of cavities and presence of thickenings, compression wood tracheids of Taxus baccata possess all the anatomical features typical of such cells, including a rounded outline, intercellular spaces, a thick S₁ layer, a highly lignified S₂ (L) layer, and no S₃ layer. Pronounced compression wood of Pseudotsuga menziesii contains helical cavities but no helical thickenings. Thickenings and cavities seem to be mutually exclusive in Pseudotsuga and Taxus.This investigation was carried out under the McIntire-Stennis Program, Cooperative State Research Service. I am indebted to Mr. A. Rezanowich of the Pulp and Paper Research Institute of Canada for kindly providing the scanning electron micrographs.     

Seasonal changes in lignin distribution during tracheid development in Pinus radiata D. Don

Summary Lignin distribution in developing tracheids of Pinus radiata was studied throughout the growth' season using quantitative interference microscopy. The pattern of lignification remained constant although the number of lignifying cells varied reaching a maximum in summer. Lignification of the secondary wall of latewood tracheids was incomplete at the onset of winter. Each stage of lignification was preceded by deposition of carbohydrates with lignification of the middle lamella starting after S1 formation and lignification of the secondary wall starting after S3 formation. Lignification of the middle lamella was completed before the start of lignin deposition in the secondary wall. In one of the trees examined, the secondary wall lignified concurrently with the middle lamella and this was associated with a low lignin concentration in the middle lamella of mature cells. The secondary wall reached a mature lignin concentration of 21–22% v/v except in one specimen containing severe compression wood which reached 28% v/v. The cell corner middle lamella reached a mature lignin concentration of 74–87% v/v.     

Studies on opposite wood in conifers part III: Distribution of lignin

Summary The distribution of lignin in opposite wood has been studied by removing the polysaccharides with hydrofluoric acid and examining the resulting lignin skeletons in the electron microscope. The thick S₃ layer was more highly lignified than the S₁ and S₂ layers in Abies balsamea, Picea rubens, Pinus resinosa, and Tsuga canadensis. In Picea rubens, but not in the other species, there was, adjacent to the S₃ layer, a transition zone in S₂ with a high concentration of lignin. The S₃ layer varied considerably in thickness and was often buckled, especially in the latewood. The structure of the bordered pits was that observed in the original wood. The margo, the torus, and the initial pit border were all highly lignified.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     

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     

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.     

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.     

A study of lignification in loblolly pine tracheids by the SEM-EDXA technique

Summary The lignification process in different morphological regions of loblolly pine tracheids was studied by the SEM-EDXA technique. Prior to S₂ layer formation, lignification was initiated in the cell corner middle lamella and compound middle lamella regions. Subsequently a rapid lignin deposition was observed in both regions, whereas secondary wall lignification was a more gradual process and initiated when the middle lamella lignin concentration was approximately 50% of maximum. Within the secondary wall, the S₁ layer is lignified first. Then, lagging just behind cell wall formation, lignification of the S₂ layer is initiated adjacent to the S₁ layer and extends toward the lumen. Finally, the S₃ layer lignified. Upon completion of lignification, the cell walls had a higher concentration of lignin in both the S₁ and S₃ layers than in the S₂ layer.This Paper is an excerpt from the Ph.D. dissertation of Shiro Saka     

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.     

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.     

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.     

Ultrastructural implications of gamma-irradiation of wood

Summary An attempt is made in this study to relate the gamma-irradiation induced degradation of wood samples to their lignin content and distribution in the cell wall. Samples of Douglas-fir and yellow-poplar were submitted to increasing doses of gamma-irradiation and subsequently extracted with a dilute NaOH solution or with DMSO, prior to SEM observation. Other samples were observed in TEM. The irradiation-extraction procedure degraded the hardwood more than the softwood. In both species, the middle lamella was more resistant than the secondary wall. The S3 layer in Douglas-fir and the warty layer in yellow-poplar appeared to be more resistant than the other secondary wall layers. Some difference was also observed in radiation stability between tracheids or fibres and ray cells. This procedure is suggested as a method for studying lignin distribution in the wood cell wall.This research was conducted as part of a thesis submitted by the first author in partial fulfilment of the requirements for the Master of Science degree at the State University of New York College of Environmental Science and Forestry, Syracuse, New York. The authors wish to thank Dr. John A. Meyer who carried out the irradiation procedure. The first author also whishes to express gratitude to the Belgian American Educational Foundation, Inc., The Fondation Francqui and Mister Charles Berolzheimer, Research Director of the California Cedar Products Company, for having provided financial support for this study     

Structure and function of flexure wood in Abies fraseri

Wood produced during flexure in one-year-old leaders of Abies fraseri (Pursh) Poir. (Fraser fir) was analyzed anatomically and radio-densitometrically. More xylem cells were produced in stems subjected to flexing than in stems that were not flexed. The lumens of tracheids produced in response to flexure were smaller than the lumens of tracheids in normal wood. This was manifest as an increase in the cell wall area/cell lumen area ratio. Microfibril orientation in flexure-induced wood approached the less extreme values found in compression wood. The growth ring composed of flexure-induced wood also had a greater density than normal wood. Compression wood, as defined by cellular characteristics observed in transverse section, was absent in flexed stems. Detailed analysis of the anatomical structure, wood density and biomechanical properties of flexure-induced wood indicated that it has more in common with compression wood than with normal 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.     

Structure of small lignin fragments retained in water-soluble polysaccharides extracted from birch MWL isolation residue

To analyze the structural features of lignin in the vicinity of lignin–carbohydrate linkages, water-soluble lignin–carbohydrate complex (LCC) with low lignin content was prepared from residual birch wood meal after the extraction of milled wood lignin (MWL). The molecular weight distribution of lignin in this LCC appeared together with carbohydrate in the relatively high molecular weight region of the gel permeation chromatogram. This result was consistent with our previous results obtained for the same fraction of Japanese cedar (sugi); however, after treatment with polysaccharide-degrading enzyme, the molecular weight distribution of carbohydrate and that of lignin shifted significantly to the lower region. These results demonstrated that molecular size of this LCC is determined by carbohydrates while lignin is present as a minor fragment in this fraction. The syringyl/guaiacyl (S/V) ratio of this LCC was higher than other lignin fractions. Ozonation analysis implied that this LCC has a relatively high number of β-1 structures. It is likely that lignin that exists near lignin–carbohydrate linkages has more endwise-type features than other lignin fractions.This paper was presented in part at the 48th Lignin Symposium, Fukui, Japan, October 2003 and at the 12th International Symposium on Wood and Pulping Chemistry, Madison, USA, June 2003     

Ultrastructure of the S2 layer in relation to lignin distribution inPinus radiata tracheids

The ultrastructure of the S₂ layer in relation to its lignin distribution was examined using transmission electron microscopy in the tracheids ofPinus radiata. The S₂ layer had a striated appearance at low magnification. Observations at higher magnifications showed lignin to be distributed inhomogeneously in this layer, appearing as a mosaic of electron-dense and electron-lucent regions. These regions are scattered, showing a pattern of often interconnecting sinuous features in a predominantly radial profile. The significance of these features of the S₂ layer is discussed, particularly in relation to the available information from recent ultrastructural observations on the appearance of cellulose microfibrils and the pattern of their distribution in the S₂ layer using rapid freeze-deep etching in conjunction with transmission electron microscopy. Predictions are made as to the likely distribution and arrangement of cellulose microfibrils in the S₂ layer based on the pattern of lignin distribution observed in this layer.     

Distribution of lignin interunit bonds in the differentiating xylem of compression and normal woods of Pinus thunbergii

The lignification process and lignin distribution at different stages of cell wall differentiation in the secondary xylem of compression and normal woods of Pinus thunbergii were investigated by thioacidolysis and subsequent desulfuration. We prepared 50-µm-thick, contiguous tangential sections of pine shoots, cut from the cambial zone through to mature xylem. In compression wood, uncondensed guaiacyl (G) and p-hydroxyphenyl (H) lignins were deposited simultaneously from early to late stages of lignification. The various types of G-G, G-H, and H-H dimers were detected in compression wood, and the ratio of G-H and H-H dimers to total dimers increased as lignification proceeded. In contrast, uncondensed and condensed H units were detected in trace amounts in normal wood. Significant differences in the relative distributions of lignin interunit linkages were not observed between compression and normal woods or between differentiating and mature xylems in either compression or normal woods.Part of this report was presented at the 10th International Symposium on Wood and Pulping Chemistry, Yokohama, June, 1999