Developmental anatomy of natural root grafts in Ficus globosa

1966 ◽  
Vol 14 (3) ◽  
pp. 269 ◽  
Author(s):  
AN Rao

The series of events, and the anatomical changes connected with them, leading to the fusion of aerial roots in Ficus globosa Blume are described. The initial contact between two aerial roots is estabiished by the formation and fusion of epidermai hairs. Secondary growth increases the size of the roots, and consequently the cortices of the two adjacent roots approach one another and become compressed. The cortical tissues thin out in the central region of the compressed zone, but fuse marginally and remain intact. In both roots the ray cells near the contact area become highly meristematic; by active division they produce many parenchyma cells that extend towards each other and finally merge to establish a continuous parenchymatous zone between the steles of the two roots. The cortical tissues, secondary phloem, and vascular cambium in both roots are interrupted by the formation of this new tissue. Later some of the parenchyma cells below the fused regions of the cortex redifferentiate into vascular cambium and extend laterally, joining the pre-existing, interrupted cambia of the two roots. Thus a continuous ring of vascular cambium is reorganized that gives rise to more secondary xylem and phloem. Cork cambium differentiates in the subepidermal layers to form a thick periderm with a smooth surface, so that the fused roots appear externally as a single root. Certain important points of the present study are discussed with reference to previous work.

IAWA Journal ◽  
1993 ◽  
Vol 14 (2) ◽  
pp. 191-204 ◽  
Author(s):  
M.N.B. Nair

The stern of Spatholobus roxburghii, a tropicalliana, has alternating layers of xylem and phloem as a result of formation and activity of successive cambia. Successive cambial rings are developed by dedifferentiation of groups of parenchyma cells outside the discontinuous band of sclereid-fibres. The sclereid- fibre band is formed by the development of sclereids between the primary bark fibres. Each successive cambium first produces a layer of sclereid-fibres which separates the vascular tissue produced by one cambial ring from the other. After secondary growth, the epidermis is replaced by periderm. In the older stern phelloderm contributes to the formation of new cambiallayers. Secondary phloem has sieve tube members; companion cells, phloem parenchyma, phloem fibres and secretory cells. The wood shows a tendency towards ring-porosity only in the first xylem layer. The subsequent layers are diffuseporous. The vessels are wide and narrow. Perforated ray cells or radial vessels are frequent in the wood and probably help in vertical conduction by interconnecting vessel endings. In this scandent species parenchyma cells are abundant. It is inferred that they help the vessel segments to remain undamaged when the woody stern twists around supports.


IAWA Journal ◽  
2017 ◽  
Vol 38 (1) ◽  
pp. 49-66 ◽  
Author(s):  
Pablo A. Cabanillas ◽  
Marcelo R. Pace ◽  
Veronica Angyalossy

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.


1975 ◽  
Vol 53 (23) ◽  
pp. 2745-2758 ◽  
Author(s):  
R. L. Peterson ◽  
E. C. Yeung

The primary phloem system in the rhizome of Hieracium floribundum has transfer cells that have developed from companion cells and parenchyma cells, which are adjacent to sieve elements. In both cell types changes occur in the cytoplasmic organelles at the time of wall ingrowth formation. Dicytosomes and polyribosomes become more numerous and 'boundary formations' and other multivesiculated structures appear. Few microtubules were found in the cytoplasm at this time. After the wall ingrowths become obvious, the transfer cells develop numerous mitochondria and an enlarged nucleus. The phloem transfer cells become vacuolated with age and the wall ingrowths become less numerous. This may be associated with a change in the translocation pattern in the phloem after the inception of vascular cambium activity. Parenchyma cells in the secondary phloem usually become rather vacuolated and develop few wall ingrowths.


1976 ◽  
Vol 54 (16) ◽  
pp. 1903-1910 ◽  
Author(s):  
Roy H. Saigo

This study examines the microscopic anatomy and seasonal changes of the secondary phloem, cambium, and a portion of the xylem of grand fir trees (Abies grandis [Dougl.] Lindl.) infested with the balsam woolly aphid (Adelges piceae Ratz.) as compared with tissues of non-infested trees.The reactivation of the vascular cambium and production of astrosclereids and resin cells are about the same in infested and non-infested trees.The infested trees exhibit sieve cells that are shorter in length, having a tangential dimension about the same as normal cells, and produce more tangential bands of phloem parenchyma cells, more fiber sclereids, biseriate rays, and lipoidal-filled ray cells, abnormally shaped ray parenchyma cell nuclei, giant cortical parenchyma cells, and traumatic resin ducts in the xylem.


2014 ◽  
Vol 69 (1) ◽  
pp. 11-20
Author(s):  
Sławomir Janakowski ◽  
Władysław Golinowski

The sclerification process in bark tissues of common fir (<em>Abies alba</em> Mill.) has been described. The sclerification begins in 3 years old stems. Sclereids differentiate from cortical parenchyma cells and from secondary phloem parenchyma cells that do not contain phenolic deposits. The first single sclereids are formed at the interface of the cortex and nonfunctional phloem. Hereafter, a continuous layer of them is formed. Later, new sclereid layers are formed successively in nonfunctional secondary phloem and cortex. The consecutive layers are separated tangentially by phloem parenchyma cells, that accumulate large amounts of phenolic substances, and by compressed phloem cells. Laterally they are separated by phloem rays that except of some dislocations are continuous. Structural net of the cortical phloem ray cells and phloem parenchyma delineates the areas where the formations of sclereid layers occurs in nonfunctional secondary phloem. Older cortex contains more sclereid layers and the time period of their formation extends continuously.


1983 ◽  
Vol 13 (1) ◽  
pp. 191-195 ◽  
Author(s):  
Cheryl R. Montain ◽  
Bruce E. Haissig ◽  
John D. Curtis

The present work describes the anatomy of adventitious root initiation in 20-day-old Pinusbanksiana Lamb, seedling cuttings propagated under intermittent mist. Shortly after cuttings were made, basal necrosis occurred in all tissues (epidermis, periderm, cortex, primary and secondary phloem, and vascular cambium) that surrounded the central xylem cylinder. Thereafter, a relatively small "callus complex" composed of parenchyma cells, a few secondary xylem tracheids, and incompletely differentiated callus vascular cambium and periderm developed at the base of cuttings. One or sometimes two root primordia initiated in the transition zone between the lowermost cortical cells of the hypocotyl and the uppermost callus parenchyma cells. Primordia invariably arose just outside one of the four axial resin canals in the hypocotyl. Results suggested that adventitious root primordia may be initiated in P. banksiana cuttings only in association with differentiated or differentiating resin canals.


IAWA Journal ◽  
1996 ◽  
Vol 17 (2) ◽  
pp. 141-150 ◽  
Author(s):  
Elsa Nunes ◽  
Teresa Quilhó ◽  
Helena Pereira

The secondary phloem of Pinus pinaster Aiton bark has sieve cells and axial and radial parenchyma, but no fibres. Resin ducts are present in fusiform rays . Stiloid crystals, starch granules and tannins occur inside sieve and parenchyma cells. The rhytidome of P. pinaster bark has a variable number of periderms forming scale-type discontinuous layers over expanded parenchyma cells. Phellem comprises 4-6 layers of thickwaIled and little suberized cells and phelloderm a layer of 2 or 3 thickened lignified ceIls and a layer of expanded cells.


IAWA Journal ◽  
2021 ◽  
pp. 1-11
Author(s):  
Kishore S. Rajput ◽  
Amit D. Gondaliya ◽  
Roger Moya

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.


1970 ◽  
Vol 48 (2) ◽  
pp. 341-359 ◽  
Author(s):  
Lalit M. Srivastava

The origin of sieve elements and parenchyma cells in the secondary phloem of Austrobaileya was studied by use of serial cross sections stained with tannic acid – ferric chloride and lacmoid. In three important respects, Austrobaileya phloem recalls gymnospermous features: it has sieve cells rather than sieve-tube members; a significant proportion of sieve elements and companion cells arise independently of each other; and sieve areas occur between sieve elements and companion cells ontogenetically unrelated to each other. The angiospermous feature includes origin of most sieve elements and parenchyma, including companion cells, after divisions in phloic initials. In these instances companion cells show a closer ontogenetic relationship to sieve elements than do other parenchyma cells. The combination of gymnospermous and angiospermous features makes phloem of Austrobaileya unique when compared to that of all those species that have been investigated in detail. It is further suggested that the term albuminous cells is inappropriate and should be replaced by companion cells but that the ontogenetic relationship implicit in the definition of companion cells is too restrictive and should be abandoned.


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