• Korean Journal of Plant Resources
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• v.11 no.3
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• pp.326-334
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• 1998

Vascular cambium in 16 species of Salicaceae is nonstoried in all of them and is made up of fusiform and ray initials. The growth of cambial girth occurred by pseudotransverse division of fusiform initials and subsequent apical intrusive growth of daughter initials. The measurements of fusiform initials in tangerntial sections have revealed that the average length varies from 252.2-437.1${\mu}{\textrm}{m}$ in investigated species, with the maximum being in Populus euramericana and the minimum in Salix purprea var. Multinervis. The length of fusiform initials depends on the length of the tapering end wall , therefore, the longer the length of the tapering end wall, therefore, the longer the length of the taperding end wall, the longer the length of fusiform initials. Ray initials have their own size, magnitude, and frequency of occrrence in each species. The relative proportion of ray initials fall about 15.0-24.5% in Salicaceae. Shrubby species of Salix have a lower ratio of ray initials than the species which possess wider trunks. New ray initials are originated from cut off the side or the end of fusiform initials and central partition of a fusiform initials.

• Journal of the Korean Wood Science and Technology
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• v.33 no.5 s.133
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• pp.1-6
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• 2005

The anatomical structure of fusiform ray was examined by scanning electron microscopy (and microscopic images were analysed by image analyser) to explain the differences in radial fluid uptake between the extremes in the radial treatment data, i.e. between the selected trees of QCI (Queen Charlotte Islands in Rhondda, South Wales) and SO (South Oregon in Dalby, North-East England) planted in the UK. The ray structure of these two seed origins was examined microscopically and different patterns of ray composition were observed. The most important anatomical features influencing radial permeability were the nature of fusiform ray, and the condition of the resin canals, epithelial cells and intercellular spaces in particular.

• Journal of Plant Biology
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• v.33 no.1
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• pp.65-72
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• 1990

An anatomical study was conducted in order to elucidate the development of primary and secondary ray in Robinia pseudoacacia L. The height of primary ray near pith decreases progressively toward periphery, while the width and number per unit area gradually increase, and then the height, width and number remain somewhat constant. Secondary ray originates from the segmentation of fusiform initials or division of the side or end of fusiform initials at the middle of the first growth layer. And after the height and width of secondary ray increases to some extent, it remains constantly.

• Journal of Plant Biology
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• v.34 no.3
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• pp.191-199
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• 1991

This study has been conducted to investigate the developmental changes of cambial initials and their derivatives in relation to the growing girth of tree in Diosypros kaki and Firmiana simplex. In D. Kaki and F. simplex with typical storeyed cambium, increase in the girth of camium occurred by radial anticlinal division in general, however occasionally the increase was companied by pseudotransverse division. The length of fusiform initials, vessel member, and sieve tube member remained relatively constant throughout the secondary growth but that of fiber showed general tendancy to increase with growing girth of tree. During the girth increase of tree, height and number of ray remained constant in D. kaki, however in F. simplex, height of ray markedly decreased while the number of ray per unit area more or less increased. The secondary ray was originated from the segmentation or division of the side or end of fusiform initials.

• Journal of the Korean Wood Science and Technology
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• v.37 no.1
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• pp.65-72
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• 2009

Variation of wood rays within a growth ring and along axial direction in Pinus koraiensis and Larix kaempferi, which are important Korean commercial softwoods, was examined to get some useful information for their effective utilization. Ray height in cell number and ray number per $0.25mm^2$ in tangential section were investigated by optical microscopy. The average heights of uniseriate rays in Pinus koraiensis and Larix kaempferi were 6.3 and 9.1 cells, respectively. The average numbers of uniseriate rays per $0.25mm^2$ in Pinus koraiensis and Larix kaempferi were 6.5 and 7.5, respectively. The average heights of fusiform rays were about 20 cells but were not significantly different in both species. From earlywood to latewood within a growth ring, the heights of uniseriate and fusiform rays decreased but their numbers remained almost constant. Along axial direction, the heights of uniseriate rays in both species increased with the increase of stem height, and the numbers of uniseriate rays per $0.25mm^2$ in Pinus koraiensis were nearly constant from 0.2 m to 5.2 m but increased up to 19.2 m beyond 5.2 m. However, a constant pattern in the numbers of uniseriate rays was not observed in Larix kaempferi. The heights of fusiform rays in both species were the highest in middle part of stems but were the lowest in base and top of trees. In conclusion, the ray variation pattern was comparatively clear within a growth ring but not clear along axial direction.

• Journal of the Korean Wood Science and Technology
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• v.15 no.2
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• pp.90-98
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• 1987

In the present paper I described the relations of wood ray indicators such as ray height, ray width, number of rays per $0.25mm^2$, ray spacing and fusiform ray height on the stem of Pinus koraiensis and Larix leptolepis grown at the Experiment Forest of Kangweon National University. The results may be summarized as follows. 1. The number of rays and ray spacing were generally decreased with the increase of ray height on the sample woods. 2. According to the tree species the patterns of varition of ray width with the increase of ray height were different, namely the relation between ray width and ray height showed some positive correlation on Pinus koraiensis and negative on Larix leptolepis. 3. It was recognized that the variation of fusiform ray height due to the increase of ray height indicated two patterns(the increasing, md constant regions) in sample woods. This boundary seemed to appear at six cells of ray height on Pinus koraiensis and ninc cells on Larix leptolepis. 4. The relation between fusiform ray height and number of rays had a negative correlation on Pinus koraiensis, but this tendancy was not obvious on Larix leptolepis. And ray spacing and ray width due to the increase of fusiform ray height were generally decreased. 5. On the whole the values of ray spacing and ray width became gradually larger in proportion to the increase of number of rays. 6. According to the increase of ray spacing the values of ray width also increased gradually. But this tendency was more clear on Pinus koraiensis than larix leptolepis.

• Journal of the Korean Wood Science and Technology
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• v.15 no.2
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• pp.79-89
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• 1987

This study was executed to examine helical structure and other feature, of Taxus cuspidata S. et Z. and Larix gmelinii var. principis-ruprechtii Pilger through photomicroscopic and scanning electron microscopic observation, and the obtained result, were summarized as follows: 1. Tracheid transition from springwood to summerwood was abrupt, mel slightly gradual in Taxus cuspidata S. et Z. and summerwood width of Larix gmelinii var. principis-ruprechtii Pilger was wider than that of Taxus cuspidata S. et Z. 2. Normal vertical and horizontal resin canals and surrounding thick epithelial cells were present in Larix gmelinii var. principis-ruprechtii Pilger but not present in Taxus cuspidata S. et Z. 3. Instead of helical thickening, helical chicks were observed only in summerwood trachieds of Larix gmelinii var. principis-ruprechtii Pilger. However, helical thickenings forming S, Z., and horizontal helix perpendicular to long axis of tracheid were observed in springood and summerwood tracheids of Taxus cuspidata S. et Z. and these helical thickenings were considered as analogous to the innermost layer of secondary wall. 4. Uniseriate and fusiform rays were appeared on tangential surface of Larix gmelinii var. principis-ruprechtii Pilger but oly uniserate ray was observed on tangential surface ot Taxus cuspidata S. et Z. The fusiform rays of Larix gmelinii var. principis-ruprechtii Pilger usually contained one horizontal resin canal bot occasionally two horizontal resin canals were contained in a fusiform ray. 5. Trabeculae and crassulae were observed in the tracheids of Larix gmelimii var. principis-ruprechtii Pilger but not observed in the tracheids of Taxus cuspidata S. et Z.

• Journal of Plant Biology
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• v.32 no.4
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• pp.305-312
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• 1989

Developmental anatomy was conducted in order to elucidate the differentiating pattern of fascicular cambial initials in the hypocotyl of Ricinus communis. The homogeneous procambium with relatively short cells in early stage is transformed into a heterogeneous structure with long and short cells in late stage in tangential view. Fusiform and ray initials are gradually originated from the long and short cells of the procambium in hypocotyl in later stage respectively. Fusiform initials are not shorter than procambial cells because of the successive elongation of vascular meristematic cells. Therefore, the distinction between procambium and fascicular cambium is not made from comparison with their cell length. The characteristics of the fascicular cambium are gradully acquired at or just after completion of hypocotyl elongation.

• Journal of Korean Society of Forest Science
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• v.78 no.2
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• pp.119-131
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• 1989

This experiment was executed to investigate and compare qualitative and quantitative anatomical features in compression wood, opposite wood, and side wood formed in a bent stem, a straight branch, and an exposed horizontal root of Korean red pine(Pinus densiflora S. et Z.). The respective four discs containing compression wood taken at 20cm interval both in stem and branch as well as a disc containing well developed compression wood from horizontal root were analyzed. Percentage of compression wood and eccentricity showed decreasing tendency with the increasing distance in height direction of stem and length direction of branch. The qualitative anatomical features of compression wood appeared to differ from those of side and opposite wood in very gradual tracheid transition from earlywood to latewood, roundish tracheid shape on cross surface, tracheid distortion at tip on radial surface, existence of intercellular space, and helical cavity in tracheid wall. And the differences in these qualitative features among the compression wood, opposite wood, and side wood became less intensive with the decreasing trends in percentage of compression wood and eccentricity. The quantitative anatomical features in compression wood also appeared to be wider in that respective widths of fusiform and uniseriate ray than those of opposite and side wood, but the heights of fusiform and uniseriate ray in compression wood were smaller than in opposite and side wood. The number of horizontal resin canal(fusiform ray) and uniseriate ray, however, showed no differences among the compression wood, opposite wood, and side wood. And the number of vertical resin canal in unit area, $4{\pi}mm^2$ of compression wood was fewer than that in opposite wood, whereas numerous vertical resin canals contained in a growth ring. These rays of compression wood seemed to be characterized by smaller height and wider width than those of opposite and side wood.

• Korean Journal of Plant Resources
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• v.11 no.3
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• pp.319-325
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• 1998

The developmental changes occuring in the secondary xylem of Aristolochia manshuriensis Komarov have been studied in different ages of vine stems. A. manshuriensis possesses typical storeyed cambium comprising both vertically elongated fusiform initials and almost isodiametric ray cell initials. Stems of A. manshuriensis have wide rays that make the secondary xylem appear dissected as other vine types. The length of vessel member and fiber remained relatively constant throughout the secondary growth. However, vessel diameter increases with the increasing age of stem till the cell reaches their maximum limit and later more or less stabilize in diameter while number of vessel per $\textrm{mm}^2$ is vice versa. Width and relative proportion of ray to axial elements gradually increased with the increasing age of stem and later remained relatively constant.