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.

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.

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.

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.

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.

Features of the Secondary Xylem that Facilitate Branch Abscission in Juvenile Wollemia Nobilis

IAWA Journal ◽  
2008 ◽  
Vol 29 (3) ◽  
pp. 225-236 ◽  
Author(s):  
R.D. Heady ◽  
G.E. Burrows
Keyword(s):  
Water Supply ◽  
Secondary Xylem ◽  
Sectional Area ◽  
Cross Sectional ◽  
First Order ◽  
Order Branch ◽  
Bordered Pits ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Parenchyma Cells

Wollemi pine (Wollemia nobilis) does not shed individual leaves but instead cleanly self-prunes the whole first-order branch with all the leaves still attached. A zone of stranded xylem at the branch base, the site of branch abscission, is described here in relation to the profusion of bordered pits and ray parenchyma cells that occur in this region. We propose that the much higher occurrence frequencies of these two features, compared to those in the stem and in the outer regions of the branch, results in a zone of radially-orientated weakness which facilitates branch abscission. We also suggest that since the stranded xylem region has a smaller cross-sectional area than the outer regions of the branch, the prevalence of bordered pits promotes water flow, and thus may alleviate the effects of this region on water supply to the foliage. Our observations represent, to the best of our knowledge, the first report of the involvement of bordered pits and ray parenchyma in branch abscission.

Effect of Ethrel on Stem Anatomy of Ulmus Americana Seedlings

IAWA Journal ◽  
1987 ◽  
Vol 8 (1) ◽  
pp. 3-9 ◽  
Author(s):  
F. Yamamoto ◽  
G. Angeles ◽  
T. T. Kozlowski
Keyword(s):  
Stem Anatomy ◽  
Ulmus Americana ◽  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Ray Cells ◽  
Dark Staining ◽  
Ray Parenchyma Cells ◽  
The Individual ◽  
Organic Deposits

Ethrel (2-chloroethylphosphonic acid) applied in lanolin paste at concentrations of 0.4, 1.6, 6.2, or 10.8% to stems of 3-month-old Ulmus americana seedlings greatly altered stem anatomy within 41 days. Application of ethrel at 1.6% or higher concentration was followed by greatly increased bark thickness primarily as a result of an increase in the amount of phloem and intercellular spaces. Xylem increment was increased following treatment with 0.4 or 1.6% ethrel and reduced by 6.2 or 10.8% ethrel. All concentrations of ethrel increased the number of vessels, reduced vessel diameters, and induced an increase in ray width and size of the individual ray cells. Ethrel at 6.2 or 10.8% inhibited differentiation of fibres, many of which were poorly developed and contained protoplasm and nucleL Ethrel also stimulated accumulation of dark-staining organic deposits in the ray parenchyma cells, axial parenchyma cells, and immature fibres. The data indicate a role of ethylene in control of growth and anatorny of stems.

Ray Structure Differences between Rootwood and Stemwood in a Range of Softwood Species

IAWA Journal ◽  
2009 ◽  
Vol 30 (1) ◽  
pp. 71-80 ◽  
Author(s):  
Pat Denne ◽  
Siân Turner
Keyword(s):  
Parenchyma Cells ◽  
Ray Parenchyma ◽  
Structural Differences ◽  
Ray Parenchyma Cells ◽  
Practical Implications ◽  
Softwood Species

Differences between the ray structure of rootwood and stemwood were analysed in 11 species from 5 families of gymnosperms. Rootwood was consistently found to have fewer ray tracheids, with ray parenchyma cells which were taller axially, wider tangentially, but shorter radially, and had more pits per cross-field than stemwood. A scale for quantifying types of cross-field pitting is proposed, and statistically significant differences in type and diameter of cross-field pitting were found between rootwood and stemwood of most species sampled. These structural differences have practical implications for identification of gymnosperm roots, and for distinguishing between rootwood and stemwood.

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