scholarly journals Development of successive cambia and wood structure in stem of Rivea hypocriteriformis (Convolvulaceae)

2016 ◽  
Vol 61 (1) ◽  
pp. 89-98 ◽  
Author(s):  
Kishore S. Rajput
Keyword(s):  
Secondary Xylem ◽  
Monsoon Season ◽  
Secondary Growth ◽  
Vascular Bundles ◽  
Growth Rings ◽  
Successive Cambia ◽  
Initial Stage ◽  
Ray Cells ◽  
Cell Layers ◽  
Ray Parenchyma Cells

Abstract This study examined the formation of successive rings of cambia in Rivea hypocriteriformis Choisy (Convolvulaceae). The mature stem is composed of four to five rings of xylem alternating with phloem. Successive cambia originate as smaller and larger segments; union and anastomosing of small cambial segments often leads to the formation of discontinuous rings. In the initial stage of growth, several vascular bundles interconnect to form the first ring of vascular cambium. The cambium remains functional for one complete season and becomes dormant during summer; a new ring of cambium is completed prior to the subsequent monsoon season and sprouting of new leaves. Successive cambia are initiated from the pericyclic parenchyma situated three to four cell layers outside of the protophloem. Functionally, all the successive cambia are bidirectional and produce secondary xylem centripetally and phloem centrifugally. The secondary xylem is diffuse-porous, with indistinct growth rings and consisting of wide fibriform vessels, fibre tracheids, and axial and ray parenchyma cells. The xylem rays are uni- to multiseriate and heterocellular. The multiseriate rays contain lignified marginal ray cells and thin-walled, unlignified central cells. The central ray cells also show accumulations of starch and druses. Discrete strands of intraxylary phloem occur at the periphery of the pith, and additional intraxylary phloem develops from adjacent cells as secondary growth progresses. Earlier-formed phloem shows heavy accumulation of callose, followed by its compaction. The development of successive cambia is correlated with extension growth and with the phenology of the plant.

Structure of the secondary xylem and development of a cambial variant in Serjania mexicana (Sapindaceae)

IAWA Journal ◽  
2021 ◽  
pp. 1-11
Author(s):  
Kishore S. Rajput ◽  
Amit D. Gondaliya ◽  
Roger Moya
Keyword(s):  
Secondary Xylem ◽  
Secondary Growth ◽  
Stem Anatomy ◽  
The Family ◽  
Ray Cells ◽  
Cambial Variant ◽  
Proportional Increase ◽  
Plant Families ◽  
Ray Parenchyma Cells ◽  
Cambial Variants

Abstract The lianas in the family Sapindaceae are known for their unique secondary growth which differs from climbing species in other plant families in terms of their cambial variants. The present study deals with the stem anatomy of self-supporting and lianescent habit, development of phloem wedges, the ontogeny of cambial variants and structure of the secondary xylem in the stems of Serjania mexicana (L.) Willd. Thick stems (15–20 mm) were characterized by the presence of distinct phloem wedges and tangentially wide neo-formed cambial cylinders. As the stem diameter increases, there is a proportional increase in the number of phloem wedges and neo-formed vascular cylinders. The parenchymatous (pericyclic) cells external to phloem wedges that are located on the inner margin of the pericyclic fibres undergo dedifferentiation, become meristematic and form small segments of cambial cylinders. These cambia extend tangentially into wide and large segments of neoformations. Structurally, the secondary xylem and phloem of the neo-formed vascular cylinders remain similar to the derivatives produced by the regular vascular cambium. The secondary xylem is composed of vessels (wide and narrow), fibres, axial and ray parenchyma cells. The occurrence of perforated ray cells is a common feature in both regular and variant xylem.

Stem anatomy at various developmental stages of secondary growth in Turbina corymbosa (Convolvulaceae)

2018 ◽  
Vol 151 (2) ◽  
pp. 219-230 ◽  
Author(s):  
Manoj M. Lekhak ◽  
Amit D. Gondaliya ◽  
Shrirang R. Yadav ◽  
Kishore S. Rajput
Keyword(s):  
Secondary Xylem ◽  
Secondary Growth ◽  
Growth Patterns ◽  
Stem Anatomy ◽  
Successive Cambia ◽  
Background Population ◽  
Short Period ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

Background – Population growth of lianas in the tropical forest is credited to their ability of CO2 sequestration and efficiency of the narrow stems to supply water required for the amount of foliage it bears. Turbina corymbosa (L.) Raf. (Convolvulaceae Juss.) is one of the fast-growing invasive species of scrambling woody lianas. It covers trees entirely within a short period to compete with above-ground resources (particularly sunlight). However, no information is available on how it manages to cope up with an increasing demand of water supply and mineral nutrients. What are the structural and developmental patterns adapted by this species to expand the stem diameter for efficient supply of below-ground resources? Therefore, our aim was to investigate the secondary growth patterns and structure of secondary xylem and phloem in T. corymbosa.Methods – Several samples of the stem with various diameters were studied using a histological method. Morphological and anatomical analyses were carried out using light microscopy.Key results – With the initiation of secondary growth, stems lose their circular outline rapidly due to unequal deposition of secondary xylem and formation of successive cambia. New successive cambia initiate from parenchymatous cells as small crescent-shaped fragments on asymmetric/opposite sides and result in a different stem conformation. Though several segments of successive cambia are formed, very few stem samples form complete cambium rings. The secondary xylem formed by successive cambia is diffuse porous with indistinct growth rings and is composed of both wide and narrow (fibriform) vessels, tracheids, fibres, axial and ray parenchyma cells. The secondary phloem consists of sieve tube elements, companion cells, axial and ray parenchyma cells. In fully grown plants, cambial action (internal cambium) occurrs between the intraxylary phloem and protoxylem and produces secondary xylem and phloem near the pith region.Conclusion – Structural alterations and unequal deposition of conducting elements, occurrence of intraxylary phloem and flattening of the stem are suggested to facilitate rapid growth of the plants by providing required minerals and nutrients. Internal cambium formed at the periphery of the pith is bidirectional and produces secondary xylem externally and intraxylary phloem internally. Continued development of intraxylary phloem from the internal cambium provides an additional path for rapid and safe translocation of photosynthates.

Traumatic Gum-Resin Cavities in the Stem of Ailanthus Excelsa Roxb.

IAWA Journal ◽  
1987 ◽  
Vol 8 (2) ◽  
pp. 167-174 ◽  
Author(s):  
A.M. Babu ◽  
G.M. Nair ◽  
J.J. Shah
Keyword(s):  
Epithelial Cells ◽  
Secondary Xylem ◽  
Ailanthus Excelsa ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Cells ◽  
Cell Layers ◽  
Ethephon Treatment ◽  
Xylem Elements ◽  
Ray Parenchyma Cells

Traumatic gum-resin cavities develop in the secondary xylem of the stem of Ailanthus excelsa Roxb. in response to fungal infection and ethephon treatment. After infection or ethephon treatment, traumatic parenchyma in several cell layers develops instead of normal secondary xylem elements. It consists of unlignified axial and ray parenchyma cells. Vessels and fibres are absent. Gum-resin cavities in one or two tangential rows develop in this tissue by the lysis of its axial parenchyma cells. The cavities are bordered by an epithelium. A few layers of traumatic parenchyma cells adjacent to the epithelial cens become meristematic and appear cambiform. The epithelial cells undergo lysis and they evidently contribute to gum-resin formation. As the lysis of epithelial cens proceeds, the adjacent cambiform cens divide to form additional epithelial cells. The process continues for some time and eventually an the axial cells of the traumatic parenchyma break down forming a tangentially anastomosing network of cavities. The cavities do not traverse the ray cells, and the multiseriate rays remain intact like bridges amidst the ramifying cavities.

Stem Anatomy and Development of Successive Cambia in the Neotropical Liana Securidaca Rivinifolia (Polygalaceae)

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 391-402 ◽  
Author(s):  
Kishore S. Rajput ◽  
Marina B. Fiamengui ◽  
Carmen R. Marcati
Keyword(s):  
Secondary Xylem ◽  
Secondary Growth ◽  
Stem Anatomy ◽  
Growth Rings ◽  
Cross Sectional ◽  
Axial Parenchyma ◽  
Successive Cambia ◽  
Bordered Pits ◽  
Perforation Plates ◽  
Diffuse Porous

The pattern of secondary growth and structure of secondary xylem was studied in the stem of the Neotropical liana Securidaca rivinifolia A. St.-Hil. (Polygalaceae). Increase in thickness of the stem was achieved by formation of successive cambia, from which initially two or three successive rings formed complete oval to circular cambia. Thereafter, the successive cambia were always crescent-shaped and never formed a complete cylinder, resulting in dumbbell-shaped cross-sectional outlines of the stems. The first successive cambium originated in the pericyclic parenchyma located outside the crushed protophloem. Prior to the development of cambium, pericyclic parenchyma formed a meristematic band of radially arranged cells. From this band, cells located in the middle of the band became the new ring of cambium. Cells on the inner face of the xylem produced by newly formed cambium differentiated into conjunctive tissue. The first elements to be differentiated from the newly developed cambium were always xylem fibres but differentiation of vessels was also observed occasionally. The xylem was diffuse porous with relatively distinct growth rings and composed of mostly solitary vessels with simple perforation plates, fibres with bordered pits, paratracheal axial parenchyma, and exclusively uniseriate rays.

scholarly journals Development of Successive Cambia and Structure of Secondary Xylem of Ipomoea Obscura (Convolvulaceae)

2014 ◽  
Vol 59 (1) ◽  
pp. 55-61 ◽  
Author(s):  
Kishore S. Rajput ◽  
Bharat D. Chaudhary ◽  
Vidya S. Patil
Keyword(s):  
Secondary Xylem ◽  
Vascular Bundles ◽  
Growth Rings ◽  
Sieve Elements ◽  
Companion Cells ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Thin Walled ◽  
Ray Parenchyma Cells ◽  
Ipomoea Obscura

Abstract Stems of Ipomoea obscura Ker Gawl., increase in thickness by forming multiple rings of cambia. Stems 5-6 mm thick produce parenchymatous derivatives which divide repeatedly to form small arcs of cambium. Several such small arcs initiate simultaneously and form a ring of small cambial arcs. After the formation of a few xylem and phloem elements, all these arcs are interconnected by transdifferentiation of parenchyma cells present between the cambial arcs and constitute a complete cambial cylinder. This newly formed cambium is functionally bidirectional: earlier- formed arcs produce xylem centripetally and phloem centrifugally, while later-formed segments exclusively produce thin-walled parenchyma cells on either side. Young stems are circular in cross section but as stem thickness increases they become oval to elliptic or lobed and dumbbell-shaped. Xylem rays are mostly uni- or biseriate and thin-walled, but multiseriate rays characteristic for a climbing habit are observed occasionally. In thick stems, the marginal ray parenchyma in most of the samples becomes meristematic and develops ray cambia which exclusively produce sieve elements. Similarly, parenchyma cells produced from later-formed cambial segments give rise to several irregularly oriented vascular bundles. The secondary xylem is diffuse porous, with indistinct growth rings and is composed of fibriform and wider vessels, fibres, and axial and ray parenchyma cells, while phloem consists of sieve elements, companion cells, and axial and ray parenchyma cells.

FORMATION OF SUCCESSIVE CAMBIA IN THE MENISPERMUM TREE COCCULUS LAURIFOLIUS (MENISPERMACEAE)

IAWA Journal ◽  
2015 ◽  
Vol 36 (4) ◽  
pp. 400-408 ◽  
Author(s):  
Kishore S. Rajput ◽  
Sangeeta Gupta
Keyword(s):  
Cell Division ◽  
Tree Species ◽  
Secondary Xylem ◽  
Vessel Diameter ◽  
Outer Side ◽  
Successive Cambia ◽  
Meristematic Cells ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

Successive cambia are often associated with the climbing or shrub habit, and is less common in trees. We studied formation of successive cambia and structure of secondary xylem in young stems of Cocculus laurifolius DC., a tree species of Menispermaceae. Cell division in the vascular cambium ceased in pencil-thick stems. Subsequently, parenchyma cells located outside the perivascular fibre cap re-differentiated and gave rise to several small segments of meristematic cells, of which the central cells divided repeatedly to initiate the first successive cambium which produces secondary xylem centripetally and phloem centrifugally. Cells located on the inner side of the newly initiated cambium differentiated into conjunctive tissue while cells on the outer side of it divided further and differentiated into sclereids. Xylem was diffuse porous and composed of vessels, fibre tracheids and ray parenchyma cells, and only differed in vessel diameter from wide-vessel climbing relatives.

Vertical and Radial Variation of Nuclear Elongation Index of Living Sapwood Ray Parenchyma Cells in a Plantation Tree of Cryptomeria Japonica

IAWA Journal ◽  
1994 ◽  
Vol 15 (3) ◽  
pp. 323-327 ◽  
Author(s):  
K.C. Yang ◽  
Y.S. Chen ◽  
C.A. Benson
Keyword(s):  
Metabolic Activity ◽  
Cryptomeria Japonica ◽  
Ground Level ◽  
Tree Crown ◽  
Growth Rings ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Cells ◽  
Elongation Index ◽  
Ray Parenchyma Cells

Vertical and radial variations of nuclear elongation index (NEI) of living sapwood ray parenchyrna cells were studied in a 45-year-old plantation tree of Cryptomeria japonica D. Don collected in Taiwan on February 27, 1992. Nine wood strips oriented in an E-W direction of the tree were collected starting at 0.3 m above ground level, and progressing upwards by 2.5 m intervals to the tree crown. Radial sections, 20 µm thick, were cut from the cambium toward the inner sapwood of these nine wood strips. The nuclear elongation index (NEI) was used to express the metabolic activity of the ray cells. It was found that metabolic activity of sapwood ray parenchyma was thc highest at the outer sapwood and declined gradually towards the inner sapwood. The lowest average NEI was found at the lowest stern level. The average NEI of various stern height levels increased with increasing stern height level. The average NEI of three growth rings at the outer sapwood near the cambium reached a maximum at the bottom of the live crown.

Structure and ontogeny of the fissured stems of Callaeum (Malpighiaceae)

IAWA Journal ◽  
2017 ◽  
Vol 38 (1) ◽  
pp. 49-66 ◽  
Author(s):  
Pablo A. Cabanillas ◽  
Marcelo R. Pace ◽  
Veronica Angyalossy
Keyword(s):  
Secondary Xylem ◽  
Vascular System ◽  
Secondary Growth ◽  
Natural Fracture ◽  
Production Rates ◽  
Axial Parenchyma ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Cambial Variant ◽  
Stem Development

Stem ontogeny and structure of two neotropical twining vines of the genus Callaeum are described. Secondary growth in Callaeum begins with a typical regular cambium that gradually becomes lobed as a result of variation in xylem and phloem production rates in certain portions of the stem aligned with stem orthostichies. As development progresses, lignified ray cells of the initially formed secondary xylem detach on one side from the adjacent tissues, forming a natural fracture that induces the proliferation of both ray and axial nonlignified parenchyma. At the same time, parenchyma proliferation takes place around the pith margin and generates a ring of radially arranged parenchyma cells. The parenchyma generated in this process (here termed disruptive parenchyma) keeps dividing throughout stem development. As growth continues, the parenchyma finally cleaves the lignified axial parts of the vascular system into several isolated fragments of different sizes. Each fragment consists of xylem, phloem and vascular cambium and is immersed in a ground matrix of disruptive parenchyma. The cambium present in each fragment divides anticlinally to almost encircle each entire fragment and maintains its regular activity by producing xylem to the centre of the fragment and phloem to the periphery. Additionally, new cambia arise within the disruptive parenchyma and produce xylem and phloem in various polarities, such as xylem to the inside and phloem to the outside of the stem, or perpendicularly to the original cambium. Unlike the very distinctive stem anatomical architecture resulting from this cambial variant in Callaeum, its secondary xylem and phloem exhibit features typical of lianas. These features include very wide conducting cells, abundant axial parenchyma, high and heterocellular rays and gelatinous fibres.

Development of cambial variant and parenchyma proliferation in Hewittia malabarica (Convolvulaceae) from India and South Africa

IAWA Journal ◽  
2020 ◽  
pp. 1-14
Author(s):  
Kishore S. Rajput ◽  
Amit D. Gondaliya ◽  
Himansu Baijnath
Keyword(s):  
South Africa ◽  
Secondary Xylem ◽  
Secondary Growth ◽  
Stem Anatomy ◽  
Histological Techniques ◽  
The Family ◽  
Ray Cells ◽  
Meristematic Activity ◽  
Cambial Variant ◽  
Interxylary Phloem

Abstract Members of the Convolvulaceae are characterized by the climbing habit and occurrence of variant secondary growth. From a histological perspective, the genus Ipomoea L. is the most extensively studied, while other genera have been less studied. Here, stem anatomy of the least studied genus in the family, Hewittia Wight & Arn., represented by Hewittia malabarica (L.) Suresh was investigated using classical histological techniques. In both the samples collected from India and South Africa, stem thickness increased by developing different types of cambial variants such as: neo-formed vascular cylinders, parenchyma proliferation at the phloem wedges, ray-derived cambia from dilating phloem rays, internal cambium, intra- and interxylary phloem. Neo-formed vascular cylinders develop from the parenchyma cells external to the phloem as a meristemoid in thick stems and later in dilating ray cells. With the increase in stem diameter, cells of the phloem wedges showed proliferation by meristematic activity, which form a connection with the cortex by rupturing the primary tissue ring of eustele. Subsequently, development of cambium in phloem wedges and deposition of its derivatives increased the tangential width of rays. Mature thick stems (25–30 mm) give rise to a fissured stem. Intraxylary (internal) phloem development on the pith margin was observed from primary growth onwards and in thick stems secondary intraxylary phloem developed from the internal cambium. Internal cambium is functionally bidirectional and produces secondary xylem internally and secondary phloem externally. In all the samples, patches of unlignified parenchyma embedded within the secondary xylem dedifferentiate and mature into interxylary phloem with the increasing age. Development of cambial variant and structure of the secondary xylem is correlated with the functional significance of the climbing habit.

CAMBIAL VARIANT AND XYLEM STRUCTURE IN THE STEM OF COCCULUS HIRSUTUS (MENISPERMACEAE)

IAWA Journal ◽  
2003 ◽  
Vol 24 (4) ◽  
pp. 411-420 ◽  
Author(s):  
Kishore S. Rajput ◽  
K.S. Rao
Keyword(s):  
Vascular Bundles ◽  
Growth Rings ◽  
Xylem Structure ◽  
Vessel Elements ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Cambial Variant ◽  
Stem Development ◽  
Cambial Cells ◽  
Cocculus Hirsutus

Development of cambial variant and xylem structure were studied in the stem of Cocculus hirsutus (Menispermaceae). In the early stages of stem development several collateral vascular bundles are joined by interfascicular cambium resulting in the formation of a complete cambial cylinder. After functioning for two to three years the cambial ring ceases its activity. Subsequently a second ring of cambium is formed from the innermost cortical parenchyma cells. These parenchyma cells undergo periclinal divisions to give rise to cells that become lignified, abaxially, and cambial cells, adaxially. The cambial cells divide periclinally giving rise to individual vascular bundles with xylem and phloem. Later the cambium in each bundle is joined by interfascicular cambium. Subsequent cambia develop similarly resulting in the formation of successive rings of xylem and phloem. During the leafless condition, all the cambial rings are dormant, and flanked by mature xylem and phloem elements. With the sprouting of new leaves, either the existing outermost cambium reactivates or an entire new ring of cambium develops. The xylem is diffuseporous with indistinct growth rings. It is composed of fibre-tracheids, tracheids, vessel elements, libriform fibres, and parenchyma cells. Xylem rays are multiseriate, compound and heterocellular. Deformed libriform fibres and vessel elements commonly occur among the ray cells in all the successive rings of xylem. The length of fibres and the height and width of xylem rays increase gradually from the centre towards the periphery of the stem.

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