Arrangement of cortical microtubules during formation of bordered pit in the tracheids ofTaxus

Summary The arrangement of cortical microtubules during the development of the secondary wall and bordered pits in the tracheids ofTaxus was examined by immunofluorescence and electron microscopy. The cambial region of radial longitudinal sections of developing young shoots (2–3 years old) contains cells at various stages of differentiation from cambial cells to tracheids. At the early stage of formation of bordered pits, circular bands of microtubules were seen to be associated with the inner edge of the border of the developing pit. In other regions than the pit secondary wall of uniform thickness was laid down, and obliquely oriented cortical microtubules ran parallel to one another. These cortical microtubules also covered the surface of the border of the developing pit on the side facing the center of the cell. As the border of the pit developed, a circular band of MTs remained associated with the inner edge of border, suggesting that the MTs were involved in the formation of the rim of the bordered pit, extending the initial border thickening, which consisted of concentrically oriented cellulose microfibrils. After completion of the formation of the bordered pit, helical thickenings became apparent. The obliquely oriented microtubules were organized in bands parallel to one another, being superimposed on the helical thickenings. The involvement of MTs in the formation of bordered pits and helical thickening is discussed.     

Tetracentron Wood from the Miocene of Noto Peninsula,Central Japan,with a short revision of homoxylic fossil woods

A vesselless fossil wood was discovered in the Miocene Yanagida Formation in the Noto Peninsula, central Japan. This fossil has distinct growth rings with gradual transition from the early- to the latewood ; tracheids, which are called 'usual traeheids' here, constitute the ground mass of the wood and have typical scalariform bordered pits on radial walls in the earlywood and circular sparse pits on those in the latewood ; rays are 1\2-4 cells wide and heterogeneous with low to high uniseriate wings; axial parenchyma strands are scattered in the latewood. This wood has a peculiar feature; sporadic radial files of broad tracheids whose tangential walls have crowded alternate bordered pits. The radial walls have crowded half-bordered pits to ray cells, but no pits to the usual tracheids. Among all of the extant and extinct angiosperms and gymnosperms, these unusual tracheids occur only in Tetracentron. From these features, we refer the fossil to the extant genus Tetracentron, and name it T. japonoxylum. A revision of homoxylic woods is made for comparision with the present fossil. Tetracentron japonoxylum is the only fossil wood of Tetracentron.     

The First Record of Fossil Wood of Winteraceae from the Upper Cretaceous of Antarctica

Fossil wood of the Winteraceae from the Upper Cretaceous sedimentsof James Ross Island, Antarctic Peninsula, is described herefor the first time. The specimen is characterized by the absenceof vessels, rays of two distinct sizes and tracheids with one–threerows of circular bordered pits, mainly on the radial walls,grading to horizontally elongate and scalariform. Despite anatomicalconformity to the family Winteraceae, the fossil wood is notidentical to any one extant genus and therefore has been assignedto the fossil organ genus Winteroxylon Gottwald with which thefossil shows greatest similarity. Copyright 2000 Annals of BotanyCompany Antarctica, Cretaceous, angiosperm, wood, anatomy, Winteraceae, Winteroxylon, fossil, palaeoclimate     

Myosin,microtubules, and microfilaments: co-operation between cytoskeletal components during cambial cell division and secondary vascular differentiation in trees

The immunolocalisation of unconventional myosin VIII ('myosin') in the cells of the secondary vascular tissues of angiosperm (Populus tremula L. x P. tremuloides Michx. and Aesculus hippocastanum L.) and gymnosperm (Pinus pinea L.) trees is described for the first time and related to other cytoskeletal elements, as well as to callose. Both myosin and callose are located at the cell plate in dividing cambial cells, whereas actin microfilaments are found alongside the cell plate; actin and tubulin are both associated with the phragmoplast. Myosin and callose also localise to the plasmodesmata-rich pit fields in the walls of living cells, which are particularly abundant within the common walls between ray cells and between ray cells and axial parenchyma cells in the phloem and xylem. In those xylem ray cells that contact developing vessel elements and tracheids, myosin, tubulin, actin and callose are localised at the periphery of developing contact and cross-field pits; the respective antibodies also highlight the bordered pits between vessels and between tracheids. The aperture of the bordered pits, whose diameter diminishes as the over-arching border of these pits develops, also houses myosin, actin and tubulin. Myosin, actin and callose are also found together around the sieve pores of sieve elements and sieve cells. We suggest that an acto-myosin contractile system (a 'plant muscle') is present at the cell plate, the sieve pores, the plasmodesmata within the walls of long-lived parenchyma cells, and at the apertures of bordered pits during their development.     

STRUCTURE OF TRACHEIDS IN THREE SPECIES OF LYCOPODIUM

The structure of tracheids in Lycopodium lucidulum, L. clavatum, and L. tristachyum was studied with the light microscope. Protoxylem development is at least sometimes and possibly always mesarch in indeterminate axes of all three species. Centrifugally formed protoxylem elements are reticulate and discontinuities in the secondary walls of these elements are sometimes conspicuously bordered. Wall thickenings of first formed protoxylem elements consist mainly of indirectly connected rings. Late centripetally formed protoxylem elements and transitional elements have a reticulate secondary wall pattern. The narrowest metaxylem elements have circular bordered pits while in wider metaxylem elements pits are bordered and may vary from circular to scalariform. Pitting is uniseriate to triseriate in tracheids of all three species, and intermittent tetraseriate pitting was occasionally observed in L. lucidulum. Crassulae occur in tracheids of the three species, and in L. clavatum an additional framework, probably representing thickened compound middle lamella, is also present. Pits often appear helically arranged, and in all three species pits are connected by thin areas in the secondary wall. Macrofibrils approximately 0.5 μ wide were observed in tracheids of the three species. In L. clavatum the arrangement of macro-fibrils was predominantly bidirectional.     

Structural analysis of K<Superscript>+</Superscript> dependence in <Emphasis Type="SmallCaps">l</Emphasis>-asparaginases from <Emphasis Type="Italic">Lotus japonicus</Emphasis>

Wood is composed of various types of cells and each type of cell has different structural and functional properties. However, the temporal and spatial diversities of cell wall components in the cell wall between different cell types are rarely understood. To extend our understanding of distributional diversities of cell wall components among cells, we investigated the immunolabeling of mannans (O-acetyl-galactoglucomannans, GGMs) and xylans (arabino-4-O-methylglucuronoxylans, AGXs) in ray cells and pits. The labeling of GGMs and AGXs was temporally different in ray cells. GGM labeling began to be detected in ray cells at early stages of S₁ formation in tracheids, whereas AGX labeling began to be detected in ray cells at the S₂ formation stage in tracheids. The occurrence of GGM and AGX labeling in ray cells was also temporally different from that of tracheids. AGX labeling began to be detected much later in ray cells than in tracheids. GGM labeling also began to be detected in ray cells either slightly earlier or later than in tracheids. In pits, GGM labeling was detected in bordered and cross-field pit membranes at early stages of pit formation, but not observed in mature pits, indicating that enzymes capable of GGM degradation may be involved in pit membrane formation. In contrast to GGMs, AGXs were not detected in pit membranes during the entire developmental process of bordered and cross-field pits. AGXs showed structural and depositional variations in pit borders depending on the developmental stage of bordered and cross-field pits.     

Modelling the hydrodynamic resistance of bordered pits

Previous studies of the hydrodynamics of plant stems have shown that resistance to flow through bordered pits on the side walls of tracheids makes up a significant proportion of their total resistance, and that this proportion increases with tracheid diameter. This suggests a possible reason why tracheids with a diameter above around 100 microm have failed to evolve. This possibility has been investigated by obtaining an estimate for the resistance of a single pit, and incorporating it into analytical models of tracheid resistance and wood resistivity. The hydrodynamic resistance of the bordered pits of Tsuga canadensis was investigated using large-scale physical models. The importance of individual components of the pit were investigated by comparing the resistance of models with different pore sizes in their pit membrane, and with or without the torus and border. The estimate for the resistance of a real bordered pit was 1.70x10(15) Pa s m(-3). Resistance of pits varied with morphology as might be predicted; the resistance was inversely proportional to the pore size to the power of 0.715; removing the torus reduced resistance by 28%, while removal of the torus and border together reduced it by 72%. It was estimated that in a 'typical tracheid' pit resistance should account for 29% of the total. Incorporating the results into the model for the resistivity of wood showed that resistivity should fall as tracheid diameter increases. However, to minimize resistance wider tracheids would also need to be proportionally much longer. It is suggested that the diameter of tracheids in conifers is limited by upper limits to cell length or cell volume. This limitation is avoided by angiosperms because they can digest away the ends of their cells to produce long, wide vessels composed of many short cells.     

The vestured pits of Eucalyptus regnans F. Muell.: a study using scanning electron microscopy

Scanning electron microscopy has been used to examine the surface architecture, before and after various chemical treatments, of the pits in the walls of vessels, vasicentric and fibre tracheids, and parenchyma cells, which together make up the wood of Eucalyptus regnans. The treatments included water at 150°C under pressure, hydrofluoric acid, delignifying agents and potassium permanganate. All bordered pits were vestured; half-bordered pits were vestured, partially vestured or non-vestured. No distinction could be made between warts and vestures on morphological or chemical grounds. An hypothesis is advanced which relates vesture formation to prolongation of the activity of the protoplast in pits as the cells die. Vestures, on the basis of this hypothesis, could be regarded as enlarged or conglomerate warts.     

水青树特殊管胞的分布位置及其形态特征的研究

针对水青树（Tetracentron sinense）中一类特殊管胞进行较为全面的观察研究,判断细胞种类并分析维管组织输导机理及树木进化过程中的细胞演化规律。通过切片和解离技术,借助光学显微镜和电子显微镜对34年生水青树特殊管胞的分布位置和形态特征进行观察。结果表明：(1)特殊管胞在树木水平方向自内向外径向呈串排列,并贯穿年轮界限,多为一列,少数两列,且较为稀见。每个特殊管胞弦向左右两侧或单侧均与木射线细胞相连通。纵向上,特殊管胞单独或数个上下端接相连。(2)特殊管胞主要有以下3种类型：无端壁的纺锤形,有一个倾斜端壁,以及有两个倾斜端壁。特殊管胞的平均长度为286.44μm;横切面为四边形,平均弦向宽度为55.22μm,其平均壁厚为1.53μm。(3)特殊管胞两端封闭,无穿孔。(4)特殊管胞侧面壁上的纹孔数量较多且纹孔膜明显可见,具体表现为：弦面壁上布满特殊管胞之间的具缘纹孔,呈对列、互列偶见梯状排列;径面壁上存在与射线细胞间的具狭缘单纹孔,呈大圆形至椭圆形,每区域多为2～10个纹孔,呈1～4排横列;径面壁上与正常管胞间几无纹孔。水青树特殊管胞分布有一定规律,其长度远小于水青树正常管胞...     

PITTING IN PSILOPHYTON DAWSONII,AN EARLY DEVONIAN TRIMEROPHYTE

Tracheids of Psilophyton dawsonii Banks, Leclercq, and Hueber 1975 from calcareous pebbles of late Early Devonian age on the Gaspé Peninsula, eastern Canada, are shown to have scalariform bordered and circular bordered pits. Macerated tracheids embedded in Spurr epoxy resin and sectioned at 2 μm; peels, ground sections, SEM and petrographic observations all indicate that interconnections between the scalariform bars are composed of secondary wall material and that the patterns produced are not artifacts of preservation. The interconnections produce a wide range of patterns from simple vertical strands, to reticula, to more extensive interconnections that outline circular openings. The circular openings result in scalariform bordered pits that are considered to be multiaperturate. P. dawsonii is believed to illustrate the most complex pitting yet demonstrated conclusively in Early Devonian time. Among trimerophytes P. forbesii, tracheids of P. charientos, and Hostinella from Röragen, Norway lack only the circular bordered pits.     

Vessel elements present in the secondary xylem of Trochodendron and Tetracentron (Trochodendraceae)

For almost 150 years, the two monotypic genera Trochodendron and Tetracentron (Trochodendraceae) have been considered to share an unusual and primitive feature in angiosperms - the lack of vessels in their wood. Therefore, they have been classified in a basal position in the angiosperms. Our observations by light microscopy, low-vacuum environmental scanning electron microscopy (ESEM) and high-vacuum scanning electron microscopy (SEM) both in fresh and FAA-fixed materials consistently showed the presence of tracheary elements differentiated into two types in both genera. In Trochodendron, the tracheary elements can be divided into perforate vessel elements and imperforate fiber-tracheids and tracheids. The vessel elements show end and lateral walls. The pits on the end walls are elongate- broadened and do not have membranes or only a few remnants of them forming the perforation plates. The fiber-tracheids show crossfield pit pairs and sharp ends, and the tracheids show bordered pits. In Tetracentron, the tracheary elements comprise vessel elements and fibers. The vessel elements are similar to those of Trochodendron, whereas the fibers have no crossfield pit pairs but, rather, elliptical pits and sharp ends. Thus, both Trochodendron and Tetracentron are vessel bearing rather than vesselless, although their vessel elements are primitive.     

Organization of Microtubules during the Transition from Cytokinesis to Interphase in Protonemal Cells of Adiantum capillus-veneris L.

The reorganization of microtubules (MTs) from cytokinesis tointerphase was examined in protonemal cells of the fern Adiantumcapillus-veneris. During the reorganization, many MTs fannedout from the nuclear envelope towards the cell periphery. Newlyformed cortical MTs were located only near the nucleus and werearranged randomly. The randomly arranged cortical MTs were thenreplaced by an interphase array of cortical MTs that were orientedpredominantly parallel to the cell axis. At the boundary betweenthe new and the old cell wall, clusters of MTs were observedafter the formation of cortical MTs. Re-formation of MTs after depolymerization of MTs was also examined.Clusters of short MTs appeared only at the nuclear envelopewhen MTs had been depolymerized by exposure of cells to 100µM propyzamide at 0°C. Few MTs were formed at theboundary between the new and old cell walls. These results suggestthat, even in fern cells, the nuclear envelope might act asMT-organizing center during the establishment of the interphasearray of MTs. (Received June 21, 1995; Accepted January 23, 1996)     

Dynamic changes in the arrangement of cortical microtubules in conifer tracheids during differentiation.

The arrangement of cortical microtubules (MTs) in differentiating tracheids of Abies sachalinensis Masters was examined by confocal laser scanning microscopy after immunofluorescent staining. The arrays of MTs in the tracheids during formation of the primary wall were not well ordered and the predominant orientation changed from longitudinal to transverse. During formation of the secondary wall, the arrays of MTs were well ordered and their orientation changed progressively from a flat S-helix to a steep Z-helix and then to a flat S-helix as the differentiation of tracheids proceeded. The orientation of cellulose microfibrils (MFs) on the innermost surface of cell walls changed in a similar manner to that of the MTs. These results provide strong evidence for the co-alignment of MTs and MFs during the formation of the semi-helicoidal texture of the cell wall in conifer tracheids.Abbreviations MT cortical microtubule - MF cellulose microfibril - S1, S2 and S3 the outer, middle and inner layers of the secondary wall The authors thank Mr. T. Itoh of the Electron Microscope Laboratory, Faculty of Agriculture, Hokkaido University, for his technical assistance. This work was supported in part by a Grant-in-Aid from the Ministry of Education, Science and Culture, Japan (no. 06404013).     

Characteristics of Wood Structure in Gymnosperms and Their systematic Significance

The systematic positions and taxonomic ranks of orders and families in Gymnosperms, especially those in Coniferopsida, are analysed and discussed in this paper based on the evolutionary trends in the wood structure. The opinions of the present authors are as follow: 1. The separation of the Araucariaceae from the Coniferae and establishment of the Araucariales are reasonable,because the intertracheid pitting in the wood is the Araucarioid type and there are no pits on both horizontal and end walls of ray parenchyma cells in the family. 2. The position of the genus Ginkgo in Cheng’s system is acceptable. Ginkgo is more similar to Coniferae than to Cycadaceae in the wood structure. 3. According to the characteristics of wood structure, arrangement of the Podocarpaceae, Cephalotaxaceae and Taxaceae between the Araucariaceae and the Pinaceae is reasonable. Among these families, the Cephalotaxaceae and Taxaceae are more closely related to each other in the view of the spiral thickenings which often appear on the inner wall of wood tracheids. 4. Further evidence for the establishment of the Sciadopitysaceae is provided. For example, most of cross-field pits in the wood of the Sciadopitysaceae are window like, while some of them are of the Lemon type or the Subtaxodioid type; bordered pits are of the Araucaria B type. 5. The characteristics of wood structure in the genus Platycladus differ greatly from Thuja. The former has cross field pits of the Cupressoid type, bordered pits of Araucaria B type and warty layer on the inner surface of tracheids. All of these characteristics have added further evidence for the separation of Platycladus from Thuja. 6. Based on the structural characteristics of woody rays in the Pinaceae, the most primitive genera are Abies, Keteleeria and Pseudolarix, while more advanced ones are Cedrus and Tsuga, and even more advanced ones are Pseudotsuga, Cathaya, Picea and Larix, all of which share normal resin canals. The most advanced genus is Pinus which is also of normal resin canals. Pinus can be divided into three subgenera, Haploxylon, Parry and Diploxylon, according to the presence or absence of dentation and warty layer in wood tracheids. 7. It is reasonable to place the genus Amentotaxus in the Taxaceae, because membrane of bordered pits in the genus is similar to that in the other four genera of the Taxaceae, both of the Araucaria type. 8. The present authors agree with Cheng’s (1978) treatment of Sect. Heopeuce in Tsuga, based on the fact that Tsuga longibracteata has traumatic resin canals and warty layer. Reducing Pinus hwangshanensis into P. taiwanensis, made by Cheng, is reasonable because of the similarities between P. hwangshanensis and P. taiwanensis in the wood structure. The establishment of a new subgenus, Patty, for Pinus bungeana is suitable based on chemotaxonomy, morphology and the distinct warty layer on the innersurface of wood tracheids.     

Changes in the Arrangement of Microtubules and Microfibrils in Differentiating Conifer Tracheids During the Expansion of Cells

The arrangements of microtubules and the cellulose microfibrilsof radial walls in tracheids of Abies sachalinensis Mastersduring the expansion of cells were examined by immunofluorescenceand field-emission scanning electron microscopy. The radialdiameter of tracheids increased to three to four times thatof cambial initial cells. Microfibrils on the innermost surfaceof primary walls of conifer tracheids at early stages were notwell ordered and most of the microfibrils were oriented longitudinally.As each cell expanded, microfibrils in the process of depositionwere still not well ordered but their orientation changed fromlongitudinal to transverse. When cell expansion ceased, microfibrilswere well ordered and oriented transversely. Cortical microtubulesshowed a change in orientation similar to that of the microfibrils.These results indicate that the orientation of cortical microtubulesis correlated with that of microfibrils as they are being laiddown and with cell morphogenesis in conifer tracheids.Copyright1995, 1999 Academic Press Microfibril, microtubule, tracheid, cell expansion, Abies sachalinensis Masters, field-emission scanning electron microscopy, immunofluorescence microscopy     

Callus of Pinus roxburghii (Chir pine) and its cytology

Callus was initiated form different vegetative parts of 3 to 5-week-old seedlings of Pinus roxburghii Sargent. Best results were obtained on Murashige and Skoog's revised medium supplemented with 4 mg1⁻¹ NAA or 2,4-D, 1 mg1⁻¹ kinetin and 15% coconut milk. Callus was grown successfully for more than a year without deterioration in its growth. Growth rate studies on the calli form cytoledon explants were undertaken with different concentrations of auxins and cytokinins. Histogenic differentiation of tracheids ocurred in all the calli, with the formation of bordered pits preceding the reticulate thickenings of the tracherary walls. Cells in the 4 to 12-week-old calli were predominantly diploid, though a few polyploid and aneuploid cells were also noticed. Chromosome bridges and laggards were observed in a number of cells.     

Orientation of Wall Microfibrils in Avena Coleoptiles and Mesocotyls and in Pisum Epicotyls

Microfibrils (MFs) on the inner surface of the walls of Avenacoleoptile and mesocotyl cells and of Pisum epicotyl cells wereexamined by a replica method. In the elongating epidermis ofthese three organs, cells having MFs that were transverse, obliqueor longitudinal to the elongation axis were intermingled. Inthe elongating parenchymal tissues, all cells deposited MFstransversely. In non-elongating cells of Avena coleoptiles andPisum epicotyls, the orientation of MFs on the inner wall surfaceof both epidermal and parenchymal cells was more longitudinalthan in elongating cells. These observations on the orientationsof MFs are compatible with those our previously reported observationson the orientations of microtubules (MT) (Iwata and Hogetsu1988). Disruption of MTs of Avena coleoptiles by treatment withamiprophosmethyl caused changes in the orientation of depositionof MFs. These results support the idea that MFs are usuallyco-aligned with MTs in organ cells and that the orientationof MFs is controlled by MTs. The averaged direction of MFs, visualized under polarized light,showed a clear difference between the epidermal and inner-tissuecell walls in the elongating regions of the three organs. Inalmost all elongating and non-elongating epidermal cells, theaveraged direction of MFs was longitudinal, while it was transversein all inner-tissue cells. (Received December 16, 1988; Accepted April 28, 1989)     

Structure of Vessels and Tracheids of Regnellidium diphyllum Lindman (Marsileaceae)

The occurrence of vessels in the root of Regnellidium diphyllumis reported and tracheids with helical and reticulate thickeningson their walls are described. The vessels in the root are helically-thickenedand they seem to have originated from helically-thickened tracheidslike the vessel members of the primary xylem of angiosperms.In the rhizome and petiole, branched tracheids are of commonoccurrence.     

Changes in the arrangement of cellulose microfibrils associated with the cessation of cell expansion in tracheids

 The relationship between the cessation of cell expansion and formation of the secondary wall was investigated in the early-wood tracheids of Abies sachalinensis Masters by image analysis and field emission scanning electron microscopy. The area of the lumen and the length of the perimeter of the lumen of differentiating tracheids increased from the cambium towards the xylem. These increases had just ceased in the case of tracheids closest to the cambium in which birefringence was first detected by observations with a polarizing light microscope. Cellulose microfibrils (MFs) deposited on the innermost surfaces of radial walls were not well ordered during the expansion of cells, but well ordered MFs were deposited at the subsequent stage of cell wall formation. The first well ordered MFs were oriented in an S-helix. The well ordered MFs had already been deposited at the tracheids where birefringence was first detected under the polarizing light microscope. These results indicate that the deposition of the well ordered MFs, namely, the formation of the secondary wall, begins before the cessation of cell expansion of tracheids. Therefore, it seems that the expansion of tracheids is restricted by the deposition of the secondary wall because the cell walls become rigid simultaneously with the development of the secondary wall and, therefore, the yield point of cell walls exceeds the turgor pressure of the cell. Received: 3 July 1996 / Accepted: 24 September 1996