دورية أكاديمية
Unveiling the mechanisms of Moso bamboo's motor function and internal growth stress.
| العنوان: | Unveiling the mechanisms of Moso bamboo's motor function and internal growth stress. |
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| المؤلفون: | Luan Y; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Yang Y; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Jiang M; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Liu H; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Ma X; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Zhang X; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Sun F; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China., Fang C; Institute of New Bamboo and Rattan Based Biomaterials, International Centre for Bamboo and Rattan (ICBR), Beijing, 100102, China.; Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing, 100102, China. |
| المصدر: | The New phytologist [New Phytol] 2024 Sep; Vol. 243 (6), pp. 2201-2213. Date of Electronic Publication: 2024 Jun 17. |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley on behalf of New Phytologist Trust Country of Publication: England NLM ID: 9882884 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-8137 (Electronic) Linking ISSN: 0028646X NLM ISO Abbreviation: New Phytol Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: Oxford : Wiley on behalf of New Phytologist Trust Original Publication: London, New York [etc.] Academic Press. |
| مواضيع طبية MeSH: | Poaceae*/physiology , Poaceae*/growth & development , Stress, Mechanical* , Stress, Physiological*, Gravitation ; Biomechanical Phenomena ; Microfibrils ; Tensile Strength |
| مستخلص: | Bamboo, a renewable resource with rapid growth and an impressive height-to-diameter ratio, faces mechanical instability due to its slender structure. Despite this, bamboo maintains its posture without breaking in its battle against environmental and gravitational forces. But what drives this motor function in bamboo? This study subjected Moso bamboo (Phyllostachys edulis) to gravitational stimulation, compelling it to grow at a 45° angle instead of upright. Remarkably, the artificially inclined bamboo exhibited astonishing shape control and adjustment capabilities. The growth strain was detected at both macroscopic and microscopic levels, providing evidence for the presence of internal stress, namely growth stress. The high longitudinal tensile stress on the upper side, along with a significant asymmetry in stress distribution in tilted bamboo, plays a pivotal role in maintaining its mechanical stability. Drawing upon experimental findings, it can be deduced that the growth stress primarily originates from the broad layers of fiber cells. Bamboo could potentially regulate the magnitude of growth stress by modifying the number of fiber cell layers during its maturation process. Additionally, the microfibril angle and lignin disposition may decisively influence the generation of growth stress. (© 2024 The Author(s). New Phytologist © 2024 New Phytologist Foundation.) |
| References: | Abasolo WP, Yoshida M, Yamamoto H, Okuyama T. 2009. Stress generation in aerial roots of Ficus elastica (moraceae). IAWA Journal 30: 216–224. Almeras T, Clair B. 2016. Critical review on the mechanisms of maturation stress generation in trees. Journal of the Royal Society Interface 13: 20160550. Almeras T, Petrova A, Kozlova L, Gril J, Gorshkova T. 2020. Evidence and quantitative evaluation of tensile maturation strain in flax phloem through longitudinal splitting. Botany 98: 9–19. Ba Z, Luo H, Guan J, Luo J, Gao J, Wu S, Ritchie RO. 2023. Robust flexural performance and fracture behavior of TiO2 decorated densified bamboo as sustainable structural materials. Nature Communications 14: 1234. Bamber RK. 1987. The origin of growth stresses: a rebuttal. IAWA Bull 8: 80–84. Bobich EG, Nobel PS. 2002. Cladode junction regions and their biomechanics for arborescent platyopuntias. International Journal of Plant Sciences 163: 507–517. Boyd JD. 1950. Tree growth stresses. III. The origin of growth stresses. Australian Journal of Scientific Research Series B: Biological Sciences 20: 294–309. Boyd JD. 1972. Tree growth stresses? Part V: evidence of an origin in differentiation and lignification. Wood Science and Technology 6: 251–262. Chen M, Guo L, Ramakrishnan M, Fei Z, Vinod KK, Ding Y, Jiao C, Gao Z, Zha R, Wang C et al. 2022. Rapid growth of Moso bamboo (Phyllostachys edulis): cellular roadmaps, transcriptome dynamics, and environmental factors. Plant Cell 34: 3577–3610. Chen M, Ye L, Li H, Wang G, Chen Q, Fang C, Dai C, Fei B. 2020. Flexural strength and ductility of Moso bamboo. Construction and Building Materials 246: 118418. Clair B, Ghislain B, Prunier J, Lehnebach R, Beauchene J, Almeras T. 2019. Mechanical contribution of secondary phloem to postural control in trees: the bark side of the force. New Phytologist 221: 209–217. Fang CH, Clair B, Gril J, Almeras T. 2007. Transverse shrinkage in G‐fibers as a function of cell wall layering and growth strain. Wood Science and Technology 41: 659–671. Fang CH, Clair B, Gril J, Liu SQ. 2008a. Growth stresses are highly controlled by the amount of G‐layer in poplar tension wood. IAWA Journal 29: 237–246. Fang CH, Guibal D, Clair B, Gril J, Liu YM, Liu SQ. 2008b. Relationships between growth stress and wood properties in poplar I‐69 (Populus deltoides Bartr. cv. “Lux” ex I‐69/55). Annals of Forest Science 65: 307. Ghislain B, Nicolini E‐A, Romain R, Ruelle J, Yoshinaga A, Alford MH, Clair B. 2016. Multilayered structure of tension wood cell walls in Salicaceae sensu lato and its taxonomic significance. Botanical Journal of the Linnean Society 182: 744–756. Goudenhooft C, Almeras T, Bourmaud A, Baley C. 2019. The remarkable slenderness of flax plant and pertinent factors affecting its mechanical stability. Biosystems Engineering 178: 1–8. Higaki A, Kadowaki Y, Yoshinaga A, Takabe K. 2021. Xylan deposition and lignification in differentiating tension wood fibers in Mallotus japonicus (Euphorbiaceae) with multi‐layered structure. Holzforschung 75: 1–12. Hiroyuki Y, Masato Y, Takashi O. 2002. Growth stress controls negative gravitropism in woody plant stems. Planta 216: 280–292. Lambers H, Chapin FS, Pons TL. 2008. Plant water relations. In: Lambers H, Chapin FS, Pons TL, eds. Plant physiological ecology. New York, NY, USA: Springer, 163–223. Li Z, Chen C, Xie H, Yao Y, Zhang X, Brozena A, Li J, Ding Y, Zhao X, Hong M et al. 2022. Sustainable high‐strength macrofibres extracted from natural bamboo. Nature Sustainability 5: 235–244. Li Z, Zhan T, Eder M, Jiang J, Lyu J, Cao J. 2021. Comparative studies on wood structure and microtensile properties between compression and opposite wood fibers of Chinese fir plantation. Journal of Wood Science 67: 12. Liese W, Grosser D. 1971. Über das Vorkommen von anomalem Gewebe in der Sproßachse von Monokotyledonen. Holz Als Roh‐Und Werkstoff 29: 339–344. Liu B, Tang L, Chen Q, Zhu L, Zou X, Li B, Zhou Q, Fu Y, Lu Y. 2022. Lignin distribution on cell wall micro‐morphological regions of fibre in developmental Phyllostachys pubescens culms. Polymers 14: 312. Luan Y, Liu L, Ma Y, Yang Y, Jiang M, Semple K, Dai C, Fei B, Fang C. 2023. An integrated hydrothermal process of bamboo flattening, densification and drying: mechanical properties and strengthening mechanisms. Materials & Design 226: 111610. Luan Y, Ma YF, Liu LT, Fei BH, Fang CH. 2022. A novel bamboo engineering material with uniform density, high strength, and high utilization rate. Industrial Crops and Products 184: 115045. Matsuo MU, Niimi G, Sujan KC, Yoshida M, Yamamoto H. 2016. Hygrothermal recovery of compression wood in relation to elastic growth stress and its physicochemical characteristics. Journal of Materials Science 51: 7956–7965. Mayr S, Cochard H. 2003. A new method for vulnerability analysis of small xylem areas reveals that compression wood of Norway spruce has lower hydraulic safety than opposite wood. Plant, Cell & Environment 26: 1365–1371. Mou Q, Hao X, Li X, Li X. 2022. Hygroexpansion behaviors of bamboo in response to moisture absorption and desorption. Construction and Building Materials 341: 127895. Palombini FL, Kindlein W Jr, de Oliveira BF, de Araujo Mariath JE. 2016. Bionics and design: 3D microstructural characterization and numerical analysis of bamboo based on X‐ray microtomography. Materials Characterization 120: 357–368. Ren W, Guo F, Zhu J, Cao M, Wang H, Yu Y. 2021. A comparative study on the crystalline structure of cellulose isolated from bamboo fibers and parenchyma cells. Cellulose 28: 5993–6005. Ren W, Zhu J, Guo F, Guo J, Wang H, Yu Y. 2022. Estimating cellulose microfibril orientation in the cell wall sublayers of bamboo through dimensional analysis of microfibril aggregates. Industrial Crops and Products 179: 114677. Ruelle J, Yoshida M, Clair B, Thibaut B. 2007. Peculiar tension wood structure in Laetia procera (Poepp.) Eichl (Flacourtiaceae). Trees‐Structure and Function 21: 345–355. Tomlinson PB. 2003. Development of gelatinous (reaction) fibers in stems of Gnetum gnemon (Gnetales). American Journal of Botany 90: 965–972. Van Soest PJ, Robertson JB, Lewis BA. 1991. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. Journal of Dairy Science 74: 3583–3597. Viljanen M, Help H, Suhonen H, Svedstrom K. 2023. Combined X‐ray diffraction tomography imaging of tension and opposite wood tissues in young hybrid aspen saplings. Wood Science and Technology 54: 797–814. Wang W, Li Y, Cai C, Zhu Q. 2023. Auxin response factors fine‐tune lignin biosynthesis in response to mechanical bending in bamboo. New Phytologist 241: 1161–1176. Zhang W, Li W, Ruan X. 2001. The growth stress of trees. World Forestry Research 14: 29–34. |
| معلومات مُعتمدة: | 1632019002 Foundation of International Centre for Bamboo and Rattan; 32071856 National Natural Science Foundation of China |
| فهرسة مساهمة: | Keywords: Bamboo; cell wall; gravitational stimulation; growth strain; growth stress; plant mechanical instability |
| تواريخ الأحداث: | Date Created: 20240618 Date Completed: 20240822 Latest Revision: 20240822 |
| رمز التحديث: | 20240822 |
| DOI: | 10.1111/nph.19913 |
| PMID: | 38887135 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1469-8137 |
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| DOI: | 10.1111/nph.19913 |