Bionic design of thin-walled structure based on the geometry of the vascular bundles of bamboo

2020 ◽  
Vol 155 ◽  
pp. 106936 ◽  
Author(s):  
Felipe Luis Palombini ◽  
Jorge Ernesto de Araujo Mariath ◽  
Branca Freitas de Oliveira
Author(s):  
D Xing ◽  
W Chen ◽  
J Ma ◽  
L Zhao

In nature, bamboo develops an excellent structure to bear nature forces, and it is very helpful for designing thin-walled cylindrical shells with high load-bearing efficiency. In this article, the cross-section of bamboo is investigated, and the feature of the gradual distribution of vascular bundles in bamboo cross-section is outlined. Based on that, a structural bionic design for thin-walled cylindrical shells is presented, of which the manufacturability is also taken into consideration. The comparison between the bionic thin-walled cylindrical shell and a simple hollow one with the same weight showed that the load-bearing efficiency was improved by 44.7 per cent.


1989 ◽  
Vol 67 (9) ◽  
pp. 2636-2645 ◽  
Author(s):  
Diane M. Erwin ◽  
Ruth A. Stockey

One small monocotyledon petiole, 1.8 × 1.5 mm wide, has been recovered from the Princeton chert in the Middle Eocene Allenby Formation, British Columbia. The petiole, rectangular in transverse outline, shows approximately 36 circular to oval-shaped vascular bundles within aerenchymatous ground tissue that includes tannin cells. The epidermis is underlain by a discontinuous hypodermis of thick-walled, pitted cells. Vascular bundles are in five series: (I) a median U-shaped arc of 11 – 13 bundles; (II) an abaxial arc of 6 bundles located below the main arc; (III) two short abaxial arcs of 3 bundles each; (IV) 2 bundles just below the abaxial surface; and (V) an adaxial series of 7 bundles that show an inverse orientation to those bundles in series I–IV. Larger bundles are collateral, with a protoxylem lacuna encircled by a ring of 9 – 14 thin-walled parenchyma cells, a relatively well-developed phloem strand, and one to three thin-walled metaxylem elements. Based on bundle arrangement, orientation, and morphology, the fossil petiole most closely resembles those of the Butomaceae and Alismataceae. This new species, Heleophyton helobiaeoides Erwin and Stockey gen. et sp.nov., in the Princeton chert flora, documents the presence of the Alismataceae in the Middle Eocene of western North America and provides further evidence that the locality represents an ancient aquatic ecosystem.


2016 ◽  
Vol 69 (4) ◽  
Author(s):  
Halyna Kalashnyk ◽  
Nataliia Nuzhyna ◽  
Maryna Gaidarzhy

<p>Three-month-old seedlings of 11 species of the subfamily Cactoideae (<em>Melocactus bahiensis</em>, <em>Melocactus curvispinus</em>, <em>Echinopsis eyriesii</em>, <em>E. mirablis</em>, <em>E. peruviana</em>, <em>Oreocereus celsianus</em>, <em>Rebutia flavistyla</em>, <em>Rebutia minuscula</em>, <em>Astrophytum myriostigma</em>, <em>Mamillaria columbiana</em>, and <em>M. prolifera</em>) have been studied. These plants exhibit a uniseriate epidermis, covered by a thin cuticle. Except for <em>E. peruviana</em> and <em>A. myriostigma</em>, no hypodermis could be detected. The shoots of all studied specimens consist mainly of cortex parenchyma with large thin-walled cells. The pith parenchyma is composed of much smaller cells. Due to the fact that the cortex parenchyma comprises the largest portion of the cross-sectional area, it can be concluded that it is the main water-storing tissue. The extent of vascular tissue development varies. Collateral vascular bundles are present in the stele. The studied seedlings contain various ergastic substances, in particular inclusions of calcium oxalate (all studied species), starch (<em>Mammillaria prolifera</em>, <em>E. mirabilis</em>, and the genus <em>Melocactus</em>), inulin-like inclusions, and occasionally lipid drops (some <em>Echinopsis</em> species).</p><p>Thus, it was found that all studied plants have a highly specialized anatomical and morphological structure. At the same time, the epidermis and hypodermis are poorly developed. Accordingly, the adaptation to arid conditions of the examined seedlings involves an increased growth of the water-storing tissue and the production of ergastic substances.</p>


In the fourth of this series of Memoirs (‘Phil. Trans.,' 1873, p. 377, et seq .) I described a remarkable plant under the name of Dictyoxylon Oldhamium ; I also gave reasons for substituting the late Mr. Gourlie ’s generic name of Lyginodendron for that of Dictyoxylon . In the same Memoir (p. 403) I referred to some petioles, to which I proposed to assign the name of Edraxylon ; but later researches demonstrated the necessity for abandoning this as a generic term and substituting for it the more comprehensive one of Rachiopteris aspera . In my Memoir, Part VI. ('Phil. Trans.,' 1874, Plate 2, p. 679, et seq .), I described this proposed Edraxylon under the name of Rachiopteris aspera . Certain similar features exhibited by the above two plants led me to remark in Memoir IV., p. 403, after showing that the Rachiopteris aspera was obviously the petiole of a Fern, “I think it far from impossible that these may prove to belong to Dictyoxylon ( Lyginodendron ) Oldhamium ; but since I have not yet succeeded in correlating them with any certainty, 1 shall add no more respecting them at present.” Since 1873 1 have accumulated a vast amount of material illustrative of the structure and relations of these two plants, and am now in a position to demonstrate that they respectively represent the stem and petiole of the same organism which proves to be a Fern. I was long under the conviction that the remarkable exogenous development of the stems of many of the Carboniferous Cryptogams, which I have so continuously demonstrated to exist, and which is now so universally recognised by Palæontologists, had no existence amongst Ferns. I have now to show that this development did exist amongst Ferns as well as amongst the arborescent Lycopods and Calamites, in which it is so conspicuous. Fig. 1 (Plate 12) is part of a transverse section of a stem or branch of Lyginodendron Oldhamium , in which a represents the medulla; b , the exogenous xylem zone; c , the place of the inner cortex, wanting in this specimen; d , one of the pairs of vascular bundles, so characteristic of the, cortex of this plant; e , the outermost cortex, composed, in transverse sections, of radiating bands of sclerenchyma, g , alternating with parenchymatous areas, f . At k, k we find two bundles of tracheids, like those at d , forming the centre of the cortical structures of a petiole of Rachiopteris aspera , i, i , which petiole is organically united to the cortex e of the Lyginodendron . The two bundles k, k are assuming the oblique relative positions seen in the similar bundles of the free petiole of R. aspera , represented in fig. 2. Other sections in my cabinet, similar to fig. 1, demonstrate the same facts, viz., that the pairs of bundles, fig. 1, d , which form so characteristic a feature of transverse sections of the middle cortex of Lyginodendrom Oldhamium , pass outwards, through the outer cortex, to become the tracheæal bundles of the petioles of the plant, and which petioles I had previously designated Rachiopteris aspera . I may state that my friend Graf Solms-Laubach, who has obtained numerous specimens of the Lyginodendron associated with others of Rachiopteris aspera from a locality on the continent, agrees with me in the conclusion at which I have arrived respecting their unity. The more perfect specimens of the Lyginodendron obtained during the last seventeen years have thrown yet further light upon those figured in 1873. In the latter, as at fig. 1, c, no traces of the middle bark were preserved; but examples from Halifax, for which I am indebted to my friends Mr. Cash and Mr. Spencer, of Halifax, have supplied what was wanting. Fig. 3 is a transverse section in which this inner cortex, c , is shown to consist of a zone of extremely delicate, thin-walled parenchymatous cells, scattered throughout which are numerous gum-canals, l . Three of these canals are represented, enlarged 250 diameters, in figs. 4 and 5, embedded in the thin-walled cells, c, c , of the cortex.


2020 ◽  
Vol 63 (2) ◽  
pp. 185-193
Author(s):  
Yuvarani Seenu ◽  
Koshila Ravi Ravichandran ◽  
Anaswara Sivadas ◽  
Balachandar Mayakrishnan ◽  
Muthukumar Thangavelu

The anatomical description of vegetative parts of Taberenaemontana alternifolia L. belonging to the family Apocynaceae was investigated in the present study. The leaves of T. alternifolia is hypostomatic with paracytic stomata, uniseriate epidermis made up of thin-walled parenchymatous cells covered by thin cuticle on both adaxial and abaxial surfaces. The hypodermis comprises of angular collenchyma cells. Mesophyll is dorsiventral containing silica bodies and vascular bundles are bicollateral. The petiole is flattened adaxially and arch-shaped abaxially with a uniseriate epidermis covered by a thin cuticle. The hypodermis is 7-8 layered angular collenchyma cells consisting of laticifers and parenchymatic, cortical layers consisting of silica bodies and thick-walled fibers and U-shaped bicollateral vascular bundles. Secondary growth in stems is characterized by the formation of periderm and thick-walled fibers in the vascular tissues. Bicollateral vascular bundles are covered by sclerenchymatous patches, parenchymatous cortex and pith consist of fibers, laticifers and silica bodies. The root possess unicellular root hairs, compactly arranged thin-walled uniseriate epidermis, 16-18 layered cortex containing silica bodies and fibers, indistinct endodermis, radially arranged vascular bundles and 14-16 arched xylem. Pitted water-storage cells are present in the conjunctive tissue. Lignin deposition was observed in the root stelar region and pith is absent.


Bothalia ◽  
1976 ◽  
Vol 12 (1) ◽  
pp. 111-117 ◽  
Author(s):  
M. F. Thompson
Keyword(s):  

The leaf and corm morphology and anatomy of representatives of the genera  Spiloxene, Pauridia and Empodium were studied. The corms are annual and tunicated, except in the group Aquaticae of Spiloxene. They are swollen stems consisting of a number of internodes. In Spiloxene and Pauridia the roots grow from the base of the corm, while in Empodium they develop from the sides. The epidermis of the older corms is replaced by several layers of thin-walled cork. Characters of the corm coverings are used to divide  Spiloxene into six groups. Four leaf forms are recognised namely carinate, terete, canaliculate and plicate. Multicellular processes and unicellular hairs occur occasionally.The leaf stomata are paracytic. Most species have mucilage canals containing pectic compounds of mucopoly­saccharides. The vascular bundles have complete or incomplete bundle sheaths and larger bundles have sclerenchyma caps.


2008 ◽  
Vol 65 (1) ◽  
pp. 11-21 ◽  
Author(s):  
L. Q. Matias ◽  
A. Soares ◽  
V. L. Scatena

The anatomical characters of the scape of Echinodorus glandulosus, E. lanceolatus, E. palaefolius, E. paniculatus, E. pubescens and E. subalatus subsp. subalatus (Alismataceae) were examined. These six sympatric species occur in northeastern Brazil and demonstrate great morphological similarity. The aim of the present study was to identify anatomical characters of taxonomic importance. Scapes possess a uniseriate epidermis composed of thin-walled tabular cells. The scapes of most species have differentiated epidermis, cortex, and vascular cylinders. There are several layers of regular chlorenchyma cells immediately below the epidermis, intercalated with collateral vascular bundles, in all species. There are also laticiferous ducts throughout the scape, and aerenchyma in both the cortex and pith. The shape and outline of scapes, the presence and position of winged extensions, the absence of differentiated vascular cylinders or cortex, and the number of vascular bundles are important characters for differentiating species in Echinodorus. An identification key employing the features analysed is provided.


2015 ◽  
Vol 88 ◽  
pp. 70-81 ◽  
Author(s):  
Shutian Liu ◽  
Zeqi Tong ◽  
Zhiliang Tang ◽  
Yang Liu ◽  
Zonghua Zhang

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