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

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.

2018 ◽  
Vol 151 (2) ◽  
pp. 219-230 ◽  
Author(s):  
Manoj M. Lekhak ◽  
Amit D. Gondaliya ◽  
Shrirang R. Yadav ◽  
Kishore S. Rajput

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.


IAWA Journal ◽  
1987 ◽  
Vol 8 (2) ◽  
pp. 167-174 ◽  
Author(s):  
A.M. Babu ◽  
G.M. Nair ◽  
J.J. Shah

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.


2014 ◽  
Vol 59 (1) ◽  
pp. 55-61 ◽  
Author(s):  
Kishore S. Rajput ◽  
Bharat D. Chaudhary ◽  
Vidya S. Patil

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.


IAWA Journal ◽  
2008 ◽  
Vol 29 (3) ◽  
pp. 225-236 ◽  
Author(s):  
R.D. Heady ◽  
G.E. Burrows

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.


IAWA Journal ◽  
2009 ◽  
Vol 30 (1) ◽  
pp. 71-80 ◽  
Author(s):  
Pat Denne ◽  
Siân Turner

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.


IAWA Journal ◽  
2008 ◽  
Vol 29 (1) ◽  
pp. 17-23 ◽  
Author(s):  
Pat Denne ◽  
Peter Gasson

Differences in ray structure between root- and stem-wood of softwoods can cause confusion in identifying roots using keys based on stem-wood anatomy. Comparison of root- and stem-wood rays of Larix decidua showed root-wood had fewer ray tracheids, taller, wider but shorter ray parenchyma cells, and larger cross-field pits than stem-wood. The implications of these differences are considered in relation to the identification and function of roots.


IAWA Journal ◽  
2000 ◽  
Vol 21 (1) ◽  
pp. 49-60 ◽  
Author(s):  
Yasuaki Sakamoto ◽  
Yuzou Sano

Water conduction and wood anatomy of Salix sachalinensis attacked by watermark disease were investigated. The internal symptom, the watermark, appeared as a brown to brown-black stained zone in sapwood. Dye injection tests revealed that water conduction did not take place in the watermark. However, soft X-ray photography and cryo-scanning electron microscopy revealed that the watermark had a high moisture level. In the watermark, some of the vessels were plugged with tyloses and masses of bacteria, and some of the ray parenchyma cells caused necrosis. Hence, the non-conductive watermark in sapwood can be considered similar to discoloured wood or wetwood.


1960 ◽  
Vol 8 (1) ◽  
pp. 51 ◽  
Author(s):  
J Cronshaw

Observstion in the electron microscope of carbon replicas of the pits of vessels, ray parenchyma cells, fibres, and tracheids of Eucalyptus regnans has shown the detailed structure of the pit borders and the pit closing membranes. In all cases in the mature wood the primary wall is left apparently without modification as the pit membrane. Unlike the borders of the pits of fibre tracheids and tracheids, the pit borders of the vessels are not separate; the cellulose microfibrils of a border may be common to several pits. The pit borders of fibre traoheids and tracheids are developed as separate entities and have a structure similar to the pit borders of softwood tracheids. The structure of the secondary wall layers associated with the pits is described and related to the structure of the pits. The fine structural features of the pits, especially of the pit closing membranes, are discussed in relation to the movement of liquids into wood.


1974 ◽  
Vol 22 (2) ◽  
pp. 211 ◽  
Author(s):  
G Scurfield ◽  
CA Anderson ◽  
ER Segnit

Scanning electron microscopy has been used to examine silica isolated by chemical means from the wood of 32 species of woody perennial. The silica consists of aggregate grains lying free in the lumina or in ray and xylem parenchyma cells in 24 of the species. It occurs as dense silica in the other species, filling the lumina or lining the internal surfaces of vessels (and fibres) in all cases except Gynotroches axillaris where it is deposited in ray parenchyma cells. Infrared spectra and X-ray diffraction diagrams, obtained for specimens of both sorts of silica, are indistinguishable from those for amorphous silica. Aggregate grain and dense silicas are also alike in that their differential thermal analysis curves show a rather broad endothermic peak between 175° and 205°C. The results are discussed in relation to possible modes of deposition of the two sorts of silica and the tendency for silica in ray parenchyma cells to be associated with polyphenols.


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