This article has multiple issues. Please help improve it or discuss these issues on the talk page. (Learn how and when to remove these template messages)(Learn how and when to remove this template message)
In vascular plants, the root is the organ of a plant that typically lies below the surface of the soil. Roots can also be aerial or aerating, that is growing up above the ground or especially above water. Furthermore, a stem normally occurring below ground is not exceptional either (see rhizome). Therefore, the root is best defined as the non-leaf, non-nodes bearing parts of the plant's body. However, important internal structural differences between stems and roots exist.
The fossil record of roots – or rather, infilled voids where roots rotted after death – spans back to the late Silurian. Their identification is difficult, because casts and molds of roots are so similar in appearance to animal burrows. They can be discriminated using a range of features.
The first root that comes from a plant is called the radicle. A root's four major functions are 1) absorption of water and inorganic nutrients, 2) anchoring of the plant body to the ground, and supporting it, 3) storage of food and nutrients, 4) vegetative reproduction and competition with other plants. In response to the concentration of nutrients, roots also synthesise cytokinin, which acts as a signal as to how fast the shoots can grow. Roots often function in storage of food and nutrients. The roots of most vascular plant species enter into symbiosis with certain fungi to form mycorrhizae, and a large range of other organisms including bacteria also closely associate with roots.
When dissected, the arrangement of the cells in a root is root hair, epidermis, epiblem, cortex, endodermis, pericycle and, lastly, the vascular tissue in the centre of a root to transport the water absorbed by the root to other places of the plant.[clarification needed]
In its simplest form, the term root architecture refers to the spatial configuration of a plant’s root system. This system can be extremely complex and is dependent upon multiple factors such as the species of the plant itself, the composition of the soil and the availability of nutrients.
The configuration of root systems serves to structurally support the plant, compete with other plants and for uptake of nutrients from the soil. Roots grow to specific conditions, which, if changed, can impede a plant's growth. For example, a root system that has developed in dry soil may not be as efficient in flooded soil, yet plants are able to adapt to other changes in the environment, such as seasonal changes.
Root architecture plays the important role of providing a secure supply of nutrients and water as well as anchorage and support. The main terms used to classify the architecture of a root system are:
- Branch magnitude: the number of links (exterior or interior).
- Topology: the pattern of branching, including:
- Herringbone: alternate lateral branching off a parent root
- Dichotomous: opposite, forked branches
- Radial: whorl(s) of branches around a root
- Link length: the distance between branches.
- Root angle: the radial angle of a lateral root’s base around the parent root’s circumference, the angle of a lateral root from its parent root, and the angle an entire system spreads.
- Link radius: the diameter of a root.
All components of the root architecture are regulated through a complex interaction between genetic responses and responses due to environmental stimuli. These developmental stimuli are categorised as intrinsic, the genetic and nutritional influences, or extrinsic, the environmental influences and are interpreted by signal transduction pathways. The extrinsic factors that affect root architecture include gravity, light exposure, water and oxygen, as well as the availability or lack of nitrogen, phosphorus, sulphur, aluminium and sodium chloride. The main hormones (intrinsic stimuli) and respective pathways responsible for root architecture development include:
- Auxin – Auxin promotes root initiation, root emergence and primary root elongation.
- Cytokinins – Cytokinins regulate root apical meristem size and promote lateral root elongation.
- Gibberellins – Together with ethylene they promote crown primordia growth and elongation. Together with auxin they promote root elongation. Gibberellins also inhibit lateral root primordia initiation.
- Ethylene – Ethylene promotes crown root formation.
Early root growth is one of the functions of the apical meristem located near the tip of the root. The meristem cells more or less continuously divide, producing more meristem, root cap cells (these are sacrificed to protect the meristem), and undifferentiated root cells. The latter become the primary tissues of the root, first undergoing elongation, a process that pushes the root tip forward in the growing medium. Gradually these cells differentiate and mature into specialized cells of the root tissues.
Growth from apical meristems is known as primary growth, which encompasses all elongation. Secondary growth encompasses all growth in diameter, a major component of woody plant tissues and many nonwoody plants. For example, storage roots of sweet potato have secondary growth but are not woody. Secondary growth occurs at the lateral meristems, namely the vascular cambium and cork cambium. The former forms secondary xylem and secondary phloem, while the latter forms the periderm.
In plants with secondary growth, the vascular cambium, originating between the xylem and the phloem, forms a cylinder of tissue along the stem and root. The vascular cambium forms new cells on both the inside and outside of the cambium cylinder, with those on the inside forming secondary xylem cells, and those on the outside forming secondary phloem cells. As secondary xylem accumulates, the "girth" (lateral dimensions) of the stem and root increases. As a result, tissues beyond the secondary phloem including the epidermis and cortex, in many cases tend to be pushed outward and are eventually "sloughed off" (shed).
At this point, the cork cambium begins to form the periderm, consisting of protective cork cells containing suberin. In roots, the cork cambium originates in the pericycle, a component of the vascular cylinder.
The vascular cambium produces new layers of secondary xylem annually. The xylem vessels are dead at maturity but are responsible for most water transport through the vascular tissue in stems and roots.
Tree roots usually grow to three times the diameter of the branch spread, only half of which lie underneath the trunk and canopy. The roots from one side of a tree usually supply nutrients to the foliage on the same side. Some families however, such as Sapindaceae (the maple family), show no correlation between root location and where the root supplies nutrients on the plant.
There is a correlation of roots using the process of plant perception to sense their physical environment to grow, including the sensing of light, and physical barriers. Over time, roots can crack foundations, snap water lines, and lift sidewalks.
The correct environment of air, mineral nutrients and water directs plant roots to grow in any direction to meet the plant's needs. Roots will shy or shrink away from dry or other poor soil conditions.
|This section does not cite any sources. (March 2010) (Learn how and when to remove this template message)|
A true root system consists of a primary root and secondary roots (or lateral roots).
- the diffuse root system: the primary root is not dominant; the whole root system is fibrous and branches in all directions. Most common in monocots. The main function of the fibrous root is to anchor the plant.
The roots, or parts of roots, of many plant species have become specialized to serve adaptive purposes besides the two primary functions[clarification needed], described in the introduction.
- Adventitious roots arise out-of-sequence from the more usual root formation of branches of a primary root, and instead originate from the stem, branches, leaves, or old woody roots. They commonly occur in monocots and pteridophytes, but also in many dicots, such as clover (Trifolium), ivy (Hedera), strawberry (Fragaria) and willow (Salix). Most aerial roots and stilt roots are adventitious. In some conifers adventitious roots can form the largest part of the root system.
- Aerating roots (or knee root or knee or pneumatophores or Cypress knee): roots rising above the ground, especially above water such as in some mangrove genera (Avicennia, Sonneratia). In some plants like Avicennia the erect roots have a large number of breathing pores for exchange of gases.
- Aerial roots: roots entirely above the ground, such as in ivy (Hedera) or in epiphytic orchids. Many aerial roots, are used to receive water and nutrient intake directly from the air - from fogs, dew or humidity in the air. Some rely on leaf systems to gather rain or humidity and even store it in scales or pockets. Other aerial roots, such as mangrove aerial roots, are used for aeration and not for water absorption. Other aerial roots are used mainly for structure, functioning as prop roots, as in maize or anchor roots or as the trunk in strangler fig. In some Epiphytes - plants living above the surface on other plants, aerial roots serve for reaching to water sources or reaching the surface, and then functioning as regular surface roots.
- Contractile roots: they pull bulbs or corms of monocots, such as hyacinth and lily, and some taproots, such as dandelion, deeper in the soil through expanding radially and contracting longitudinally. They have a wrinkled surface.
- Coarse roots: Roots that have undergone secondary thickening and have a woody structure. These roots have some ability to absorb water and nutrients, but their main function is transport and to provide a structure to connect the smaller diameter, fine roots to the rest of the plant.
- Fine roots: Primary roots usually <2 mm diameter that have the function of water and nutrient uptake. They are often heavily branched and support mycorrhizas. These roots may be short lived, but are replaced by the plant in an ongoing process of root 'turnover'.
- Haustorial roots: roots of parasitic plants that can absorb water and nutrients from another plant, such as in mistletoe (Viscum album) and dodder.
- Propagative roots: roots that form adventitious buds that develop into aboveground shoots, termed suckers, which form new plants, as in Canada thistle, cherry and many others.
- Proteoid roots or cluster roots: dense clusters of rootlets of limited growth that develop under low phosphate or low iron conditions in Proteaceae and some plants from the following families Betulaceae, Casuarinaceae, Elaeagnaceae, Moraceae, Fabaceae and Myricaceae.
- Stilt roots: these are adventitious support roots, common among mangroves. They grow down from lateral branches, branching in the soil.
- Storage roots: these roots are modified for storage of food or water, such as carrots and beets. They include some taproots and tuberous roots.
- Structural roots: large roots that have undergone considerable secondary thickening and provide mechanical support to woody plants and trees.
- Surface roots: These proliferate close below the soil surface, exploiting water and easily available nutrients. Where conditions are close to optimum in the surface layers of soil, the growth of surface roots is encouraged and they commonly become the dominant roots.
- Tuberous roots: A portion of a root swells for food or water storage, e.g. sweet potato. A type of storage root distinct from taproot.
The distribution of vascular plant roots within soil depends on plant form, the spatial and temporal availability of water and nutrients, and the physical properties of the soil. The deepest roots are generally found in deserts and temperate coniferous forests; the shallowest in tundra, boreal forest and temperate grasslands. The deepest observed living root, at least 60 metres below the ground surface, was observed during the excavation of an open-pit mine in Arizona, USA. Some roots can grow as deep as the tree is high. The majority of roots on most plants are however found relatively close to the surface where nutrient availability and aeration are more favourable for growth. Rooting depth may be physically restricted by rock or compacted soil close below the surface, or by anaerobic soil conditions.
|Species||Location||Maximum rooting depth (m)||References|
|Boscia albitrunca||Kalahari desert||68||Jennings (1974)|
|Juniperus monosperma||Colorado Plateau||61||Cannon (1960)|
|Eucalyptus sp.||Australian forest||61||Jennings (1971)|
|Acacia erioloba||Kalahari desert||60||Jennings (1974)|
|Prosopis juliflora||Arizona desert||53.3||Phillips (1963)|
Certain plants, namely Fabaceae, form root nodules in order to associate and form a symbiotic relationship with nitrogen-fixing bacteria called rhizobia. Due to the high energy required to fix nitrogen from the atmosphere, the bacteria take carbon compounds from the plant to fuel the process. In return, the plant takes nitrogen compounds produced from ammonia by the bacteria.
The term root crops refers to any edible underground plant structure, but many root crops are actually stems, such as potato tubers. Edible roots include cassava, sweet potato, beet, carrot, rutabaga, turnip, parsnip, radish, yam and horseradish. Spices obtained from roots include sassafras, angelica, sarsaparilla and licorice.
Sugar beet is an important source of sugar. Yam roots are a source of estrogen compounds used in birth control pills. The fish poison and insecticide rotenone is obtained from roots of Lonchocarpus spp. Important medicines from roots are ginseng, aconite, ipecac, gentian and reserpine. Several legumes that have nitrogen-fixing root nodules are used as green manure crops, which provide nitrogen fertilizer for other crops when plowed under. Specialized bald cypress roots, termed knees, are sold as souvenirs, lamp bases and carved into folk art. Native Americans used the flexible roots of white spruce for basketry.
Tree roots can heave and destroy concrete sidewalks and crush or clog buried pipes. The aerial roots of strangler fig have damaged ancient Mayan temples in Central America and the temple of Angkor Wat in Cambodia.
Vegetative propagation of plants via cuttings depends on adventitious root formation. Hundreds of millions of plants are propagated via cuttings annually including chrysanthemum, poinsettia, carnation, ornamental shrubs and many houseplants.
Roots can also protect the environment by holding the soil to prevent soil erosion. This is especially important in areas such as sand dunes.
- Absorption of water
- Cypress knee
- Drought rhizogenesis
- Fibrous root system
- Mycorrhiza – root symbiosis in which individual hyphae extending from the mycelium of a fungus colonize the roots of a host plant.
- Plant physiology
- Rhizosphere – region of soil around the root influenced by root secretions and microorganisms present
- Root cutting
- Rooting powder
- Tanada effect
- Retallack, G. J. (1986). "The fossil record of soils". In Wright, V. P. Paleosols: their Recognition and Interpretation (PDF). Oxford: Blackwell. pp. 1–57.
- Hillier, R.; Edwards, D.; Morrissey, L.B. (2008). "Sedimentological evidence for rooting structures in the Early Devonian Anglo–Welsh Basin (UK), with speculation on their producers". Palaeogeography, Palaeoclimatology, Palaeoecology. 270 (3–4): 366–380. doi:10.1016/j.palaeo.2008.01.038.
- Malamy, J. E. (2005). "Intrinsic and environmental response pathways that regulate root system architecture". Plant, Cell & Environment. 28: 67–77. doi:10.1111/j.1365-3040.2005.01306.x.
- Caldwell, M. M., Dawson, T. E., & Richards, J. H. (1998). Hydraulic lift: consequences of water efflux from the roots of plants. Oecologia, 113(2), 151-161.
- Fitter, A. H (1991). "The ecological significance of root system architecture: an economic approach". In Atkinson, D. Plant Root Growth: An Ecological Perspective. Blackwell. pp. 229–243.
- Malamy, J. E.; Ryan K. S. (2001). "Environmental regulation of lateral root initiation in Arabidopsis". Plant Physiology. 127: 899–909.
- Nakagawa, Y.; Katagiri, T.; Shinozaki, K.; Qi, Z.; Tatsumi, H.; Furuichi, T.; Kishigami, A.; Sokabe, M.; Kojima, I.; Sato, S.; Kato, T.; Tabata, S.; Iida, K.; Terashima, A.; Nakano, M.; Ikeda, M.; Yamanaka, T.; Iida, H. (2007). "Arabidopsis plasma membrane protein crucial for Ca2+ influx and touch sensing in roots". Proceedings of the National Academy of Sciences. 104 (9): 3639–3644. doi:10.1073/pnas.0607703104.
- UV-B light sensing mechanism discovered in plant roots, San Francisco State University, December 8, 2008
- Hodge, A. (2012). "Plant Root Interactions". In Witzany, G.; Baluska, F. Biocommunication of Plants. Springer. pp. 157–169. ISBN 978-3-642-23523-8.
- "Want bigger plants? Get to the root of the matter". Society for Experimental Biology. 2012.
- Carminati, Andrea; Vetterlein, Doris; Weller, Ulrich; Vogel, Hans-Jörg; Oswald, Sascha E. (2009). "When roots lose contact". Vadose Zone Journal. 8 (3): 805–809. doi:10.2136/vzj2008.0147.
- Nowak, Edward J.; Martin, Craig E. (1997). "Physiological and anatomical responses to water deficits in the CAM epiphyte Tillandsia ionantha (Bromeliaceae)". International Journal of Plant Sciences. 158 (6): 818–826. JSTOR 2475361.
- Pütz, Norbert (2002). "Contractile roots". In Waisel Y.; Eshel A.; Kafkafi U. Plant roots: The hidden half (3rd ed.). New York: Marcel Dekker. pp. 975–987.
- Canadell, J.; Jackson, R. B.; Ehleringer, J. B.; Mooney, H. A.; Sala, O. E.; Schulze, E.-D. (December 3, 2004). "Maximum rooting depth of vegetation types at the global scale". Oecologia. 108 (4): 583–595. doi:10.1007/BF00329030.
- Stonea, E. L.; P. J. Kaliszb (1 December 1991). "On the maximum extent of tree roots". Forest Ecology and Management. 46 (1–2): 59–102. doi:10.1016/0378-1127(91)90245-Q.
- Postgate, J. (1998). Nitrogen Fixation (3rd ed.). Cambridge, UK: Cambridge University Press.
- Zahniser, David (February 21, 2008) "City to pass the bucks on sidewalks?" Los Angeles Times
- Dennis D.Baldocchi and Liukang Xu. 2007. What limits evaporation from Mediterranean oak woodlands – The supply of moisture in the soil, physiological control by plants or the demand by the atmosphere? Vol 30, issue 10. Elsevier
- Brundrett, M. C. 2002. Coevolution of roots and mycorrhizas of land plants. New phytologist 154(2): 275–304. (Available online: DOI | Abstract | Full text (HTML) | Full text (PDF))
- Chen, R., E. Rosen, P. H. Masson. 1999. Gravitropism in Higher Plants. Plant Physiology 120 (2): 343–350. (Available online: Full text (HTML) | Full text (PDF)) – article about how the roots sense gravity.
- Clark, Lynn. 2004. Primary Root Structure and Development – lecture notes
- Coutts, M. P. 1987. Developmental processes in tree root systems. Canadian Journal of Forest Research 17: 761–767.
- Raven, J. A., D. Edwards. 2001. Roots: evolutionary origins and biogeochemical significance. Journal of Experimental Botany 52 (Suppl 1): 381–401. (Available online: Abstract | Full text (HTML) | Full text (PDF))
- Schenk, H. J., and R. B. Jackson. 2002. The global biogeography of roots. Ecological Monographs 72 (3): 311–328.
- Sutton, R. F., and R. W. Tinus. 1983. Root and root system terminology. Forest Science Monograph 24 pp 137.
- Phillips, W. S. 1963. Depth of roots in soil. Ecology 44 (2): 424.
- Caldwell, M. M., Dawson, T. E., & Richards, J. H. (1998). Hydraulic lift: consequences of water efflux from the roots of plants. Oecologia, 113(2), 151-161.
|Wikimedia Commons has media related to Roots.|
- Cite error: The named reference
:0was invoked but never defined (see the help page).