• Title/Summary/Keyword: interfascicular cambium

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Development and Ultrastructure of Interfascicular Cambium in Stem of Ginkgo biloba Seedling (은행나무 유직물의 줄기에서 유관동문 형성층의 발생과 미세구조)

  • Soh, Woong Young
    • Journal of Plant Biology
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    • v.38 no.3
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    • pp.281-288
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    • 1995
  • The progressive differentiation of interfascicular cambium from residual meristem in the first internode of Ginkgo biloba seedlings was elucidated by light and electron microscopy. The cells of residual meristem were small and homogeneous and heterogeneous in their arrangement but those of the adjacent cortex and pith were large and homogeneous. Some interprocambial residual meristem progressively became elongated and vacuolated during the process of the differentiation. In tangential section, residual meristem composed of long and short cells. The eventual interfascicular cambium had long fusiform initials and short ray initials. Storage materials in the cells progressively disappeared from the interprocambial residual meristem and were absent in early interfascicular cambium. Both the radial and tangential walls of cells of the interprocambial residual meristem were almost the same, but the radial wall became progressively thicker than the tangential wall during differentiation of interfascicular cambium. From these results, it is clear that interfascicular cambium is gradually differentiated from residual meristem.

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Origin and Development of the Interfascicular Cambium from Residual Meristem in Seed Plants (종자식물 잔존분열조직으로부터 유관속간형성층의 기원과 발생)

  • 소웅영
    • Journal of Plant Biology
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    • v.35 no.3
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    • pp.273-281
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    • 1992
  • The origin of the interfascicular cambium from residual meristem can be elucidated by tangential and transverse observation. It is clear that there is structural distinction between interprocambial and interfascicular residual meristem and adjacent parenchyma in both the transverse and tangential view. Consequently, the residual meristem does not convert into parenchyma but, rather, becomes interfascicular cambium. In tangential view, the homogeneous structure of interfascicular residual meristem at an early stage changes gradually into a heterogeneous one at a later stage, with long and short cells from which fusiform and ray initials originate respectively. However, the homogeneous structure of parenchyma adjacent interfascicular residual meristem does not change into a heterogeneous one but remains the same at all stages of development. Therefore, the interfascicular cambium has a direct ontogenetic continuity with the residual meristem, and does not have its secondary origin from differentiated parenchyma. Furthermore, the ontogenetic pattern of the interfascicular cambium is almost the same as that of fascicular cambium.ambium.

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Anatomical Studies on Root Formation in Hypocotyl and Epicotyl Cuttings of Woody Plants (임목(林木)의 배축(胚軸) 및 유경삽수발근(幼茎揷穗発根)의 해부학적(解剖学的) 연구(研究))

  • Choi, Man Bong
    • Journal of Korean Society of Forest Science
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    • v.52 no.1
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    • pp.1-30
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    • 1981
  • The origin and development of adventitious roots was studied using hypocotyl and epicotyl cuttings of 34 species, 24 genus of woody plants. These cuttings obtained from young seedlings cultured in vials containing distilled water only. The several characteristics of cuttings materials studied are shown in Table 1. The results are summerized as follows: 1. The circumference shapes of cross-sections of hypocotyl and epicotyl cuttings can be divided into six categories, namely, round, irregular round, ellipse, irregular ellipse, square, and triangle. Species differences within a genus did not show any difference of hypocotyl and epicotyl cross-sections shape, however, a noticeable variation among genus or higher taxa. 2. The arrangements of vascular bundles in the cross-sections of hypocotyls or epicotyls were almost all collateral types and generally showed generic characteristics differing one to the other. However, there were some variations between species within the genus. Six models of vascular bundle arrangement were proposed for all the above speices. 3. The rooting portions of hypocotyl and epicotyl cuttings in this experimental materials can be grouped as follows: (1) Interfascicular parenchyma; (Thuja orientalis. T. orientalis for. sieboldii, Acer microsieboldianum, A. palmatum, A. saccharinum, Cercis chinensis, Lespedeza bicolor, Magnolia obovata, M. sieboldii, Mallotus japonicus, Staphylea bumalda) (2) Cambial and phloem parenchyma: (Chamaecyparis obtusa, C. pisifera, Albizzia julibrissin, Buxus microphylla var. Koreana, Cereis chinensis, Euonymus japonica, Firmiana platanifolia, Lagerstroemia indica, Ligustrum salicinum, L. obtusifolium, Magnolia kobus, M. obovata, Mallotus japonicus, Morus alba, Poncirus trifoliata, Quercus myrsinaefolia, Rosa polyantha, Styrax japonica, Styrax obassia) (3) Primary ray tissues; (Euonymus japonica, Styrax japonica) (4) Leaf traces; (Quercus acutissima, Q. aliena) (5) Cortex parenchyma; (Ailanthus altissima) (6) Callus tissues; (Castanea crenata, Quercus aliena, Q. myrsinaefolia, Q. serrata) 4. As a general tendency throughout the species studied, in hypocotyl cuttings, the adventitious root primordia were originated from the interfascicular parenchyma tissue, however, leaf traces and callus tissues were contributed to the root primordia formation in epicotyl cuttings. The hypocotyl cuttings of Ailanthus altissima exhibited a special performance in the root primordia formation, this means that cortex parenchyma was participated to the origin tissue. And in Firmiana platanifolia, differening from the other most species, the root primordia were formed at the phloem parenchyma adjacent outwardly to xylem tissue of vascular bundle system as shown photo. 48. 5. All the easy-to, or difficult-to root species developed adventitious roots in vials filled with distilled water. In the difficult-to-root species, however, root formations seemed to be delayed because they almost all had selerenchyma or phloem fiber which gave some mechanical hindrance to protrusion of root primordia. On the other hand, in the easy-to-root species they seemed to form them more easily because they did not have the said tissues. The rooting portions between easy-to-root and difficult-to-root species have not clearly been distinguished, and they have multitudinous variations. 6. The species structured with the more vascular bundles in number compared with the less vascular bundles exhibited delayed rooting. In the cuttings preparation, the proximal end of cuttings was closer to root-to-stem transition region, the adventitious root formation showed easier. 7. A different case occured however with the mature stem cuttings, in both the needle-leaved and the broad-leaved species. In the hypocotyl cuttings, parenchymatous tissues sited near the vascular bundles become the most frequent root forming portions in general and relevant distinctions between both species were hardly recognizable. 8. In the epicotyl cuttings, root primordia originated mainly in leaf traces in connection with cambial and phloems or callus tissues itself. In the hypocotyl cuttings, interfascicular parenchyma was the most frequent portion of the root primordia formation. The portions of root primordia had more connection with vascular cambium system, as the tissues were continuing to be developed.

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