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In vascular plants, the root is an organ that typically (but not always) lies below the surface of the soil. Roots are found in various modifications and forms, but have in common a particular vascular structure that distinguishes them from other plant organs. In most cases root cells do not contain chloroplasts.
but this is not always the case, since a root can also be aerial (that is, growing above the ground) or aerating (that is, growing up above the ground or especially above water). On the other hand, a stem normally occurring below ground is not exceptional either (see rhizome). So, it is better to define root as a part of a plant body that bears no leaves, and therefore also lacks nodes. There are also important internal structural differences between stems and roots. The two major functions of roots are 1) absorption of water and inorganic nutrients and 2) anchoring the plant body to the ground. Roots also function in cytokinin synthesis, which supplies some of shoot needs. They often function in storage of food.
Roots serve three major functions in plant growth: the absorbtion of water and nutrients, anchoring the plant in place, and as a food storage organ.
Nutrients are absorbed from the surrounding solution in the surrounding soil or water passively through simple osmosis or actively using a cation exchange process.
For terrestrial plants, roots anchor the plant to the soil. For floating aquatic plants, roots act as a ballast or floatation organ, keeping the shoot above the water line or just below it, facing upward to collect sunlight. For aerial plants (epiphytes), roots anchor the plant to the branch or other object the plant is attached to.
In most plants, the root is the primary storage site for starches. In terrestrial plants, storing starch in the root system helps the plant survive if the shoot it removed by grazing, fire, or mechanical means such as wind or human activity.
- Aerial roots
- Storage organs
- Oxygenating organs
At the tip of every growing root is a conical covering of tissue called the root cap. It usually is not visible to the naked eye. It consists of undifferentiated soft tissue (parenchyma) with unthickened walls covering the apical meristem. The root cap provides mechanical protection to the meristem cells as the root advances through the soil, its cells worn away but quickly replaced by new cells generated by cell division within the meristem. The root cap is also involved in the production of mucigel, a sticky mucilage that coats the new formed cells. These cells contain statoliths, starch grains that move in response to gravity and thus control root orientation.
The outside surface of a primary root is the epidermis. Recently produced epidermal cells absorb water from the surrounding environment and produce outgrowths called root hairs that greatly increase the cell's absorptive surface. Root-hairs are very delicate and generally short-lived, remaining functional for only a few days. However, as the root grows, new epidermal cells emerge and these form new root hairs, replacing those that die. The process by which water is absorbed into the epidermal cells from the soil is known as osmosis. For this reason, water that is saline is more difficult for most plant species to absorb.
Beneath the epidermis is the cortex, which comprises the bulk of the primary root. Its main function is storage of starch. Intercellular spaces in the cortex aerate cells for respiration. An endodermis is a thin layer of small cells forming the innermost part of the cortex and surrounding the vascular tissues deeper in the root. The tightly packed cells of the endodermis contain a substance known as suberin in their cell walls. This suberin layer is the Casparian strip, which creates an impermeable barrier of sorts. Mineral nutrients can only move passively within root cell walls until they reach the endodermis. At that point, they must be actively transported across a cell membrane to continue further into the root. This allows the plant to accumulate mineral nutrients in the stele.
The vascular cylinder, or stele, consists of the cells inside the endodermis. The outer part, known as the pericycle, surrounds the actual vascular tissue. In monocotyledonous plants, the xylem and phloem cells are arranged in a circle around a pith or center, whereas in dicotyledons, the xylem cells form a central "hub" with lobes, and phloem cells fill in the spaces between the lobes.
All roots have primary growth or growth in length. Roots of many vascular plants, especially dicots and gymnosperms, often undergo secondary growth, which is an increase in diameter. A vascular cambium forms in the stele to produce secondary phloem and secondary xylem. The epidermis is replaced by a periderm. As the stele increases in diameter, the cortex, pericycle and endodermis are lost. Even nonwoody roots often undergo secondary growth, including those of tomato and alfalfa.
Early root growth is a function 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 sacrificed to protect the meristem), and undifferentiated root cells. The latter will 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.
Roots will generally grow in any direction where the correct environment of air, mineral nutrients and water exists to meet the plant's needs. Roots will not grow in dry soil. Over time, given the right conditions, roots can crack foundations, snap water lines, and lift sidewalks. At germination, roots grow downward due to gravitropism, the growth mechanism of plants that also causes the shoot to grow upward. In some plants (such as ivy), the "root" actually clings to walls and structures.
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 cambium layer 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.
Types of roots
A true root system consists of a primary root and secondary roots (or lateral roots).
The primary root originates in the radicle of the seedling. During its growth it rebranches to form the lateral roots. Generally, two categories are recognized:
- the taproot system: the primary root is prominent and has a single, dominant axis; there are fibrous secondary roots running outward. Usually allows for deeper roots capable of reaching low water tables. Most common in dicots. The main function of the taproot is to store food.
- 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 described in the introduction.
- Adventitous roots arise from the stem and not from another root. They usually 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.
- Aerating roots (or pneumatophores): roots rising above the ground, especially above water such as in some mangrove genera (Avicennia, Sonneratia)
- Aerial roots: roots entirely above the ground, such as in ivy (Hedera) or in epiphytic orchids. They function as prop roots, as in maize or anchor roots or as the trunk in strangler fig.
- Buttress roots or tabular roots: support roots for many tropical tree species
- 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.
- 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 adventitous 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, Eleagnaceae, 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.
- Tuberous roots: A portion of a root swells for food or water storage, e.g. sweet potato and dahlia. A type of storage root distinct from taproot.
The distribution of vascular plant roots within the soil depends on plant life form, and the spatial and temporal availability of water and nutrients in 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 m below the ground surface, was observed during the excavation of an open-pit mine in Arizona, USA.
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, sasparilla 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.
- Rooting Powder
- Mycorrhiza - root symbiosis in which individual hyphae extending from the mycelium of a fungus colonize the roots of a host plant.
- Fibrous root system
- 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
- 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.
- Phillips, W.S. 1963. Depth of roots in soil. Ecology 44 (2): 424.