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1.
Hebanthe eriantha (Poir.) Pedersen, a climbing species of the Amaranthaceae increases in stem thickness by forming successive cambia. The family is dominated by herbaceous species and is constantly under discussion due to its disputed nature of the meristem. In the young stem small alternate segments of vascular cambium cease to divide and new arc of cambium initiates outside to it. The newly formed arcs connect with pre-existing alternate segments of cambium to complete the ring. On the contrary, in thick stems, instead of small segments, complete ring of cambium is replaced by new one. These new alternate segments/cambia originate from the parenchyma cells located outside to the phloem produced by previous cambium. Cambium is storied and exclusively composed of fusiform initials while ray cells remain absent at least in the early part of the secondary growth. However, large heterocellular rays are observed in 15-mm diameter stems but their frequency is much lower. In some of the rays, ray cells become meristematic and differentiate into radially arranged xylem and phloem elements. In fully grown plants, stems are composed of several successive rings of secondary xylem alternating with secondary phloem. Secondary xylem is diffuse-porous and composed of vessels, fibres, axial parenchyma while exceptionally large rays are observed only in the outermost regions of thick stems. Vessel diameter increases progressively from the centre towards the periphery of stems. Although the origin of successive cambia and composition of secondary xylem of H. eriantha remains similar to other herbaceous members of Amaranthaceae, the occurrence of relatively wider and thick-walled vessels and large rays in fully grown plants is characteristic to climbing habit.  相似文献   

2.
Ipomoea hederifolia stems increase in thickness using a combination of different types of cambial variant, such as the discontinuous concentric rings of cambia, the development of included phloem, the reverse orientation of discontinuous cambial segments, the internal phloem, the formation of secondary xylem and phloem from the internal cambium, and differentiation of cork in the pith. After primary growth, the first ring of cambium arises between the external primary phloem and primary xylem, producing secondary phloem centrifugally and secondary xylem centripetally. The stem becomes lobed, flat, undulating, or irregular in shape as a result of the formation of both discontinuous and continuous concentric rings of cambia. As the formation of secondary xylem is greater in one region than in another, this results in the formation of a grooved stem. Successive cambia formed after the first ring are of two distinct functional types: (1) functionally normal successive cambia that divide to form secondary xylem centripetally and secondary phloem centrifugally, like other dicotyledons that show successive rings, and (2) abnormal cambia with reverse orientation. The former type of successive rings originates from the parenchyma cells located outside the phloem produced by previous cambium. The latter type of cambium develops from the conjunctive tissue located at the base of the secondary xylem formed by functionally normal cambia. This cambium is functionally inverted, producing secondary xylem centrifugally and secondary phloem centripetally. In later secondary growth, xylem parenchyma situated deep inside the secondary xylem undergoes de‐differentiation, and re‐differentiates into included phloem islands in secondary xylem. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 30–40.  相似文献   

3.
Successive cambia in Aizoaceae: products and process   总被引:1,自引:0,他引:1  
The transverse and longitudinal sections of the stems and roots of 11 genera of Aizoaceae, representing a wide range of growth forms from hard fibrous stems to fibre‐free roots, were studied using light microscopy and scanning electron microscopy. In most of the genera, fibres are the first xylary product of each vascular cambium, followed by vessels in a parenchyma background. Variations on this pattern help to prove that fibres are produced by vascular cambia, except in Ruschia and Stayneria, in which both the lateral meristem and the vascular cambia produce fibres. Cylinders of conjunctive tissue parenchyma that alternate with the vascular cylinders are produced by the lateral meristem. The concept that the lateral meristem gives rise to the vascular cambia and secondary cortex is supported by photographic evidence. Radial divisions occur in the origin of the lateral meristem, and then again as vascular cambia arise from the lateral meristem; these radial divisions account for storeying in fibres and conjunctive tissue. Raylessness characterizes all Aizoaceae studied, with the exception of Tetragonia, which also differs from the remaining genera by having vasicentric axial parenchyma, a scattering of vessels amongst fibres, and the presence of druses instead of raphides. Several vascular cambia are typically formed per year. Several vascular cambia are active simultaneously in a given stem or root. Roots have fewer fibres and more abundant conjunctive tissue parenchyma than stems. Successive cambia result in an ideal dispersion of vascular tissue with respect to water and photosynthate storage and retrieval capabilities of the parenchyma, and to liana stem plans. The distribution and relative abundance of fibres, vessels, secondary phloem, and conjunctive tissue parenchyma relate primarily to habit and are not a good source of systematic data, with the probable exception of Tetragonia. The general pattern of lateral meristem and vascular cambial ontogeny is the same as in other families of the core Caryophyllales, although the patterns of the tissues produced are diverse. © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society, 2007, 153 , 141–155.  相似文献   

4.
5.
Quantitative and qualitative data are presented for woods of 30 species of woody Polygonaceae. Wood features that ally Polygonaceae with Plumbaginaceae include nonbordered perforation plates, storeying in narrow vessels and axial parenchyma, septate or nucleate fibres, vasicentric parenchyma, pith bundles that undergo secondary growth, silica bodies, and ability to form successive cambia. These features are consistent with pairing of Plumbaginaceae and Polygonaceae as sister families. Wood features that ally Polygonaceae with Rhabdodendraceae include nonbordered perforation plates, presence of vestured pits in vessels, presence of silica bodies and dark-staining compounds in ray cells, and ability to form successive cambia. Of the features listed above, nonbordered perforation plates and ability to form successive cambia may be symplesiomorphies basic to Caryophyllales sensu lato . The other features are more likely to be synapomorphies. Wood data thus support molecular cladograms that show the three families near the base of Caryophyllales s.l. Chambered crystals are common to three genera of the family and may indicate relationship. Ray histology suggests secondary woodiness in Antigonon, Atraphaxis, Bilderdykia, Dedeckera, Eriogonum, Harfordia, Muehlenbeckia, Polygonum , and Rumex . Other genera of the family show little or no evidence of secondary woodiness. Molecular data are needed to confirm this interpretation and to clarify the controversial systematic groupings within the family proposed by various authors. Vessel features of Polygonaceae (lumen diameter, element length, density, degree of grouping) show an extraordinary range from xeromorphy to mesomorphy, indicating that wood has played a key role in ecological and habital shifts within the family; the diversity in ecology and habit are correlated with quantitative wood data.  © 2003 The Linnean Society of London. Botanical Journal of the Linnean Society , 2003, 141 , 25−51.  相似文献   

6.
In Ipomoea hederifolia Linn., stems increase in thickness by forming successive rings of cambia. With the increase in stem diameter, the first ring of cambium also gives rise to thin-walled parenchymatous islands along with thick-walled xylem derivatives to its inner side. The size of these islands increases (both radially and tangentially) gradually with the increase in stem diameter. In pencil-thick stems, that is, before the differentiation of a second ring of cambium, some of the parenchyma cells within these islands differentiate into interxylary phloem. Although all successive cambia forms secondary phloem continuously, simultaneous development of interxylary phloem was observed in the innermost successive ring of xylem. In the mature stems, thick-walled parenchyma cells formed at the beginning of secondary growth underwent dedifferentiation and led to the formation of phloem derivatives. Structurally, sieve tube elements showed both simple sieve plates on transverse to slightly oblique end walls and compound sieve plates on the oblique end walls with poorly developed lateral sieve areas. Isolated or groups of two to three sieve elements were noticed in the rays of secondary phloem. They possessed simple sieve plates with distinct companion cells at their corners. The length of these elements was more or less similar to that of ray parenchyma cells but their diameter was slightly less. Similarly, in the secondary xylem, perforated ray cells were noticed in the innermost xylem ring. They were larger than the adjacent ray cells and possessed oval to circular simple perforation plates. The structures of interxylary phloem, perforated ray cells, and ray sieve elements are described in detail.  相似文献   

7.
Mature stems of Sesuvium sesuvioides (Fenzl) Verdc. were found to be composed of successive rings of xylem alternating with phloem. Repeated periclinal divisions in the parenchyma outside the primary phloem gave rise to conjunctive tissue and the lateral meristem that differentiate into the vascular cambium on its inner side. After the formation of the vascular cambium, the lateral meristem external to it became indistinct as long as the cambium was functional. As the cambium ceased to divide, the lateral meristem again became apparent prior to the initiation of the next cambial ring. The cambium was exclusively composed of fusiform cambial cells with no rays. In the young saplings, the number of cambial cylinders in the axis varied from the apex to the base, indicating formation of several rings within the year. In each successive ring of the lateral meristem, small segments differentiated into the vascular cambium and gave rise to vessels, axial parenchyma, fibres and fibriform vessels towards the inside, and secondary phloem on the outer side. In the old stems, non‐functional phloem of the innermost rings was replaced by a new set of sieve tube elements formed by periclinal divisions in the cambial segments associated with the non‐functional phloem. In some places the cambial segments completely differentiate into derivatives leaving no cambial cells between the xylem and phloem. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 548–555.  相似文献   

8.
The wood anatomical structure of 11 out of 13 genera from four tribes of the Vaccinioideae, namely Andromedeae s.s. , Gaultherieae, Lyonieae and Oxydendreae (Ericaceae s.l. ), is described using light and scanning electron microscopy. Several features of the secondary xylem support the tribal classification based on molecular data: arrangement of vessel-ray pitting, height of multiseriate rays and the shape of the body ray cells. Oxydendreae are clearly defined from the other representatives by various wood anatomical features. Gaultherieae can be distinguished from Lyonieae by differences in vessel perforation plates, vessel-ray pitting, height and structure of multiseriate rays, and occurrence of prismatic crystals, but the wood of Andromedeae s.s. is similar to Gaultherieae. Moreover, Andromedeae s.s. , Oxydendreae and Vaccinieae are characterized by their pith structure, whereas considerable variation in the pith cells is found in Lyonieae and Gaultherieae.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 144 , 161–179.  相似文献   

9.
Stem flattening in Rhynchosia pyramidalis (Fabaceae) is achieved by the development of crescent-shaped successive cambia on two opposite sides of the stem (referred hereafter as distal side). Other lateral sides of the stem (adjacent to supporting host and its opposite side, referred as proximal sides) usually possess single cambium. In the young stems, parenchymatous cells located outside to protophloem of distal side dedifferentiate and develop small segments of cambium. Concomitant to bidirectional differentiation of the secondary xylem and phloem, these newly developed cambial segments also extend in tangential directions. Differential activity of newly developed crescent-shaped cambial segments deposits more secondary xylem at median position as compared to their terminal ends of the stem on distal side; consequently, it pushes the cambial segment outside, thus resulting in crescent-shaped arcs of the cambia only on two opposite sides. After the production of 1–2 mm of secondary xylem, they cease to divide and new segments of cambial arc develop on the same side in a similar fashion. Such repeated behaviour of successive cambia development consequently leads to the formation of tangentially flat stems. The secondary xylem is diffusely porous with indistinct growth rings and is composed of vessels (wide and narrow), fibres, axial ray parenchyma cells, while phloem consisted of sieve elements, companion cells, axial and ray parenchyma. Rays in both xylem and phloem are uni- to multiseriate and heterocellular. The structure of secondary xylem and development of successive cambia is correlated with climbing habit.  相似文献   

10.
Raylessness occurs in several hundred species belonging to about 40 families (fewer depending on taxonomic delineation). Fibre distribution (raylessness at first, followed by origin of rays), fibre wall thickness and sclerenchyma at pith margins support the idea that rapid acquisition of mechanical strength is basic to most instances of raylessness. Raylessness may be the most readily available process for achieving mechanical strength in ancestrally herbaceous groups lacking large amounts of phloem and cortical fibres. Raylessness is not a uniform phenomenon and a small number of instances suggest alternative causation, as in two lianas (Cobaea, Thunbergia). Raylessness occurs in only a small number of trees and annuals, but is found in woody herbs, subshrubs and some shrubs. It is indicative of secondary woodiness and wood paedomorphosis. Raylessness would seem to block the radial flow that rays typically provide, but a surprising number of rayless woods have moderately pitted fibres (indicative of flow) and septate or non‐septate living fibres. Three‐dimensional networks of conjunctive tissues in rayless species with successive cambia (Aizoaceae, Amaranthaceae, Nyctaginaceae) could also provide radial flow avenues. Ontogenetic changes from raylessness to ray presence within the stem of a given species are described and illustrated. Pseudo‐raylessness, late‐onset raylessness and early‐onset raylessness are recognized. Systematic distribution and pertinent literature are given for known instances of raylessness and pseudo‐raylessness. Raylessness shows that wood evolution involves not merely change in the abundance and position of cell types, but also redesign and diversification in cell types. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 178 , 529–555.  相似文献   

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