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Plant Taxonomy
Plantae
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Explore the diversity of with One Species at a Time, EOL's podcast series.
Each short audio story focuses on species and the scientists who study them, include multimedia extras and relevant educational resources.
Our podcasts are hosted by Ari Daniel Shaprio and produced by Atlantic Public Media
One Species at a Time Podcast Series
License | http://creativecommons.org/licenses/by/3.0/ |
Rights holder/Author | Tracy Barbaro, Tracy Barbaro |
Source | podcast.eol.org |
Root systems control erosion: vascular plants
Root systems of plants control erosion through architectural characteristics.
"A distinction is usually made between mechanical and hydrological effects of roots without much focus on the influence of architectural characteristics on these effects. Some commonly used architectural characteristics are the spatial distribution of root area ratio for slope stability analysis and root density or root length density for analysis of water erosion control. But many other architectural features, such as the branching pattern, root orientation and fractal characteristics, seem empirically and intuitively related to the effect of root systems on erosion phenomena. Many links between root system architectural characteristics and their soil fixing effects probably do exist and more links could be identified. However, most of these links remain very weak and empirical. The research which is needed to make these relationships explicit is still poorly developed and mainly focused on resistance against uprooting by wind loading. Moreover, although the mechanical and hydrological mechanisms of soil-root interaction are rather well described for simple processes such as sheet, rill or interrill erosion, this knowledge is almost nonexistent for complex processes such as gully erosion. This hampers understanding the importance of root system architecture for these processes." (Reubens et al. 2007:398-399)
Learn more about this functional adaptation.
- Reubens, B.; Poesen, J.; Danjon, F.; Geudens, G.; Muys, B. 2007. The role of fine and coarse roots in shallow slope stability and soil erosion control with a focus on root system architecture: a review. Trees-Structure and Function. 21(4): 385-402.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/93f9fcfba6da81f945a49a4f9e57af48 |
Wood resists fracture: trees
Wood of trees resists crosswise fracture via complex architecture.
"That construction of lengthwise tubes with relatively modest cross-connections gives wood its spectacular anisotropy…Crosswise, though, most woods resist fracture well, with the highest work of fracture of any rigid biological material; the orientational difference can be as much as a hundredfold (table 15.7). Not only can we use all kinds of intrusive fasteners such as nails and screws without initiating fracture, but a tree can be injured by a crosswise ax stroke and yet not crack in the next storm. A sawyer must cut almost all the way across the trunk before a healthy tree topples." (Vogel 2003:343)
Learn more about this functional adaptation.
- Steven Vogel. 2003. Comparative Biomechanics: Life's Physical World. Princeton: Princeton University Press. 580 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/a0393af7c0fd1892630b1639b2eb4c3a |
Red leaves hide plants from insects: plants
Anthocyanins in leaves camouflage the plant from insects and make insects more vulnerable to predators by inhibiting the reflecting of green wavelengths.
"Hence, leaf anthocyanins by closing the green reflectance window left by chlorophyll make the leaf less discernible to insect consumers (plant camouflage hypothesis). Alternatively (or in addition), the usually green folivorous insects, if found on a red leaf, are more easily recognized by their predators (undermining of insect camouflage by the plant)…The neglected hypothesis of plant camouflage against herbivory and the recent opinion that leaf redness may undermine the green folivorous insect camouflage are theoretically more sound since they are compatible with folivorous insect vision physiology and also afford a reasonable explanation for the almost exclusive selection of red anthocyanins in leaves." (Manetas 2006:172)
Learn more about this functional adaptation.
- Manetas, Y. 2006. Why some leaves are anthocyanic and why most anthocyanic leaves are red?. Flora: Morphology, Distribution, Functional Ecology of Plants. 201(3): 163-177.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/41485cdf8b83c1fd210b5b1c66e9c052 |
Leaves resist bending: trees
The leaves of many plants are flat yet flexible surfaces that resist bending thanks to structural features and bracing from below.
"The main use of flat surfaces in nature consists of photosynthetic structures such as leaves. These also are well braced beneath; most leaves seem to circumvent problems of loads perpendicular to their surfaces simply by flexing or reorienting in winds (fig. 1.5). Quite a few leaves of various lineages (mostly monocots) use a slight longitudinal V-fold to get adequate flexural stiffness, which must also give them nicely low torsional stiffness. Other leaves use another deviation from flatness, crosswise fan folding, discussed by Niklas (1992). Figure 21.8 shows a few such schemes." (Vogel 2003:439)
[Caption for Figure 21.8 in Vogel 2003: "Thin leaf surfaces avoid bending in various ways. Veins may provide supporting trusses (a), the whole leaf may be cambered lengthwise (b), or pleats can make a ridge-and-valley self-trussing system (c)."]
Learn more about this functional adaptation.
- Steven Vogel. 2003. Comparative Biomechanics: Life's Physical World. Princeton: Princeton University Press. 580 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/19624d85b7189ebb04992f356b517652 |
Thylakoidal system transports folded proteins: plants
Thylakoids of plants and cyanobacteria are able to transport folded or malformed proteins across tightly sealed membranes via a protein translocation system.
"A subset of lumen proteins is transported across the thylakoid membrane by a Sec-independent translocase that recognizes a twin-arginine motif in the targeting signal. A related system operates in bacteria, apparently for the export of redox cofactor-containing proteins. In this report we describe a key feature of this system, the ability to transport folded proteins. The thylakoidal system is able to transport dihydrofolate reductase (DHFR) when an appropriate signal is attached, and the transport efficiency is almost undiminished by the binding of folate analogs such as methotrexate that cause the protein to fold very tightly. The system is moreover able to transport DHFR into the lumen with methotrexate bound in the active site, demonstrating that the ΔpH-driven transport of large, native structures is possible by this pathway. However, correct folding is not a prerequisite for transport. Truncated, malfolded DHFR can be translocated by this system, as can physiological substrates that are severely malfolded by the incorporation of amino acid analogs." (Hynds et al. 1998:34868)
Learn more about this functional adaptation.
- Hynds, P. J.; Robinson, D.; Robinson, C. 1998. The Sec-independent Twin-arginine Translocation System Can Transport Both Tightly Folded and Malfolded Proteins across the Thylakoid Membrane. Journal of Biological Chemistry. 273(52): 34868-34874.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/922c216b8a3e4b39113691723ecd50cd |
Investing resources increases competitive success: trees
The investment of resources for structural support in trees allows for competitive success by prolonging the reproductive life of the organism.
"The development of the 'tree' habit in many different plant families must reflect a high degree of competitive success for this life form. The expenditure of materials in short supply in the production of long-lived, mechanically robust forms must confer survival benefits to such plants. Synthesis of materials for mechanical support of the plant uses resources that otherwise might have been directed towards reproduction. We see an elegant use of strengthening tissues that parallels engineering solutions. Although expensive in mechanical tissues, the tree habit prolongs the period over which an individual may produce seed; over a long period successful seed formation and germination is more likely." (Cutler 2005:98)
Learn more about this functional adaptation.
- Cutler, DF. 2005. Design in plants. In: Collins, MW; Atherton, MA; Bryant, JA, editors. Nature and Design. Southampton, Boston: WIT Press. p 95-124
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/34965116efe1740bb2b99fe2d14069d9 |
Pollen survives extreme dehydration: flowering plants
Pollen of flowering plants can survive extreme dehydration via several mechanisms, including a reversible wall-folding pathway that results in complete impermeability.
"Upon release from the anther, pollen grains of angiosperm flowers are exposed to a dry environment and dehydrate. To survive this process, pollen grains possess a variety of physiological and structural adaptations. Perhaps the most striking of these adaptations is the ability of the pollen wall to fold onto itself to prevent further desiccation. Roger P. Wodehouse coined the term harmomegathy for this folding process in recognition of the critical role it plays in the survival of the pollen grain. There is still, however, no quantitative theory that explains how the structure of the pollen wall contributes to harmomegathy. Here we demonstrate that simple geometrical and mechanical principles explain how wall structure guides pollen grains toward distinct folding pathways. We found that the presence of axially elongated apertures of high compliance is critical for achieving a predictable and reversible folding pattern. Moreover, the intricate sculpturing of the wall assists pollen closure by preventing mirror buckling of the surface. These results constitute quantitative structure-function relationships for pollen harmomegathy and provide a framework to elucidate the functional significance of the very diverse pollen morphologies observed in angiosperms." (Katifori et al. 2010:7635)
Learn more about this functional adaptation.
- Chaffey N. 2010. Plant Cuttings. Annals of Botany. 105(6): v-viii.
- Katifori E; Alben S; Cerda E; Nelson DR; Dumais J. 2010. Foldable structures and the natural design of pollen grains. PNAS. 107(17): 7635-9.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/4b947bd393964caaa1290cd77d0bb10b |
Catalysts facilitate water-splitting: plants
Plants get the charge needed for photosynthesis by holding water molecules in place to facilitate proton and electron transfer using catalysts.
"To replicate one of the important steps in natural photosynthesis, Brookhaven chemists James Muckerman and Dmitry Polyansky have turned to molecular complexes containing metals such as ruthenium that can drive the conversion of water into oxygen, protons, and electrons. These ruthenium catalysts hold water molecules in place to make oxygen bonds while the protons and electrons are transferred among the molecules and the catalyst, providing the charges necessary to continue the photosynthesis process." (ScienceDaily 2007)
Learn more about this functional adaptation.
- ScienceDaily. 2007. Artificial Photosynthesis: Inspired By Nature, Scientists Explore Pathways To Clean, Renewable Solar Fuel.
http://www.sciencedaily.com/releases/2007/03/070327144459.htm.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/91e5a4d13b854e1aafce47c06347ff57 |
Sclereid cells prevent soft tissue collapse: plants
Sclereid cells in vascular plants help prevent the collapse of soft tissues during water stress via thick, lignified walls.
"Sclereids are also cells with thick, lignified walls. They are grouped with fibres under the general term sclerenchyma. They differ from fibres in generally being shorter in relation to their length, but there is some overlap in the range of cells. They may be branched, sinuous or short -- often more or less isodiametric. The longer ones commonly feature in the sheaths to veins, particularly near the ends of the finer branches. They can be pit-prop-like when they extend between the upper and lower surfaces of leaves, and appear to help prevent collapse of softer tissues at times of water stress, as in olive leaves and the leaves of many mangrove plants. These plants, and many of the hard-leaved plants found in arid habitats, often have abundant elongated or branched sclereids." (Cutler 2005:104)
Learn more about this functional adaptation.
- Cutler, DF. 2005. Design in plants. In: Collins, MW; Atherton, MA; Bryant, JA, editors. Nature and Design. Southampton, Boston: WIT Press. p 95-124
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/2d4c836b145676f98ca471fa5fba8449 |