Information about Xylem
In vascular plants, xylem is one of the two types of transport tissue, phloem being the other one. The word "xylem" is derived from classical Greek ξυλον (xylon), "wood", and indeed the best known xylem tissue is wood, though it is found throughout the plant. Its basic function is to transport water.
The most distinctive cells found in xylem are the tracheary elements: tracheids and vessel elements. However, the xylem is a complex tissue of plants, which means that it includes more than one type of cell. In fact, xylem contains other kinds of cells, such as parenchyma, in addition to those that serve to transport water.
Secondary xylem, also known as Metaxylem, is the xylem that is formed during secondary growth from vascular cambium. Secondary xylem is also found in members of the "gymnosperm" groups Gnetophyta and Ginkgophyta and to a lesser extent in members of the Cycadophyta. The two main groups in which secondary xylem can be found are:
In most plants, pitted tracheids function as the primary transport cells. The other type of tracheary element, besides the tracheid, is the vessel element. Vessel elements are joined by perforations into vessels. In vessels, water travels by bulk flow, like in a pipe, rather than by diffusion through cell membranes. The presence of vessels in xylem has been considered to be one of the key innovations that led to the success of the angiosperms[2]. However, the occurrence of vessel elements is not restricted to angiosperms, and they are absent in some archaic or "basal" lineages of the angiosperms: (e.g., Amborellaceae, Tetracentraceae, Trochodendraceae, and Winteraceae), and their secondary xylem is described by Arthur Cronquist as "primitively vesselless". Cronquist considered the vessels of Gnetum to be convergent with those of angiosperms[3]. Whether the absence of vessels in basal angiosperms is a primitive condition is contested, the alternative hypothesis being that vessel elements originated in a precursor to the angiosperms and were subsequently lost.
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Physiology of xylem
The xylem transports water from the root up the plant. The xylem is mainly responsible for the transportation of water and mineral nutrients throughout the plant. Xylem sap consists mainly of water and inorganic ions, although it can contain a number of organic chemicals as well. This transport is not powered by energy spent by the tracheary elements themselves, which are dead at maturity and no longer have living contents. Two phenomena cause xylem sap to flow:- Transpirational pull: the most important cause of xylem sap flow, is caused by the evaporation of water from the surface mesophyll cells to the atmosphere. This transpiration causes millions of minute menisci to form in the cell wall of the mesophyll. The resulting surface tension causes a negative pressure in the xylem that pulls the water from the roots and soil.
- Root pressure: If the water potential of the root cells is more negative than the soil, usually due to high concentrations of solute, water can move by osmosis into the root. This may cause a positive pressure that will force sap up the xylem towards the leaves. In extreme circumstances the sap will be forced from the leaf through a hydathode in a phenomenon known as guttation. Root pressure is most common in the morning before the stomata open and cause transpiration to begin. Different plant species can have different root pressures even in a similar environment; examples include up to 145 kPa in Vitis riparia but around zero in Celastrus orbiculatus[1].
Anatomy of xylem
Xylem can be found:- in vascular bundles, present in non-woody plants and non-woody plant parts
- in secondary xylem, laid down by a meristem called the vascular cambium
- as part of a stelar arrangement not divided into bundles, as in many ferns.
The most distinctive cells found in xylem are the tracheary elements: tracheids and vessel elements. However, the xylem is a complex tissue of plants, which means that it includes more than one type of cell. In fact, xylem contains other kinds of cells, such as parenchyma, in addition to those that serve to transport water.
Primary and Secondary xylem
Primary xylem, also known as Protoxylem, is the xylem that is formed during primary growth from procambium.Secondary xylem, also known as Metaxylem, is the xylem that is formed during secondary growth from vascular cambium. Secondary xylem is also found in members of the "gymnosperm" groups Gnetophyta and Ginkgophyta and to a lesser extent in members of the Cycadophyta. The two main groups in which secondary xylem can be found are:
- conifers (Coniferae): there are some six hundred species of conifers. All species have secondary xylem, which is relatively uniform in structure throughout this group. Many conifers become tall trees: the secondary xylem of such trees is marketed as softwood.
- angiosperms (Angiospermae): there are some quarter of a million to four hundred thousand species of angiosperms. Within this group secondary xylem has not been found in the monocots. In the remainder of the angiosperms this secondary xylem may or may not be present, this may vary even within a species, depending on growing circumstances. In view of the size of this group it will be no surprise that no absolutes apply to the structure of secondary xylem within the angiosperms. Many non-monocot angiosperms become trees, and the secondary xylem of these is marketed as hardwood.
Evolution of xylem
Xylem appeared early in the history of terrestrial plant life. Fossil plants with anatomically preserved xylem are known from the Silurian (more than 400 million years ago), and trace fossils resembling individual xylem cells may be found in earlier Ordovician rocks. The earliest true and recognizable xylem consists of tracheids with a helical-annular reinforcing layer added to the cell wall. This is the only type of xylem found in the earliest vascular plants, and this type of cell continues to be found in the protoxylem (first-formed xylem) of all living groups of plants. Several groups of plants later developed pitted tracheid cells, apparently through convergent evolution. In living plants, pitted tracheids do not appear in development until the maturation of the metaxylem (following the protoxylem).
In most plants, pitted tracheids function as the primary transport cells. The other type of tracheary element, besides the tracheid, is the vessel element. Vessel elements are joined by perforations into vessels. In vessels, water travels by bulk flow, like in a pipe, rather than by diffusion through cell membranes. The presence of vessels in xylem has been considered to be one of the key innovations that led to the success of the angiosperms[2]. However, the occurrence of vessel elements is not restricted to angiosperms, and they are absent in some archaic or "basal" lineages of the angiosperms: (e.g., Amborellaceae, Tetracentraceae, Trochodendraceae, and Winteraceae), and their secondary xylem is described by Arthur Cronquist as "primitively vesselless". Cronquist considered the vessels of Gnetum to be convergent with those of angiosperms[3]. Whether the absence of vessels in basal angiosperms is a primitive condition is contested, the alternative hypothesis being that vessel elements originated in a precursor to the angiosperms and were subsequently lost.
See also
- cohesion-tension theory
- phloem
- secondary growth
- transpirational pull
- vascular tissue
- vascular bundle
References
1. ^ Tim J. Tibbetts; Frank W. Ewers (2000). "Root pressure and specific conductivity in temperate lianas: exotic Celastrus orbiculatus (Celastraceae) vs. native Vitis riparia (Vitaceae)". American Journal of Botany 87: 1272-78.
2. ^ Carlquist, S.; E.L. Schneider (2002). "The tracheid–vessel element transition in angiosperms involves multiple independent features: cladistic consequences" 89: 185-195.
3. ^ Cronquist, A. (Aug 1988.). The Evolution and Classification of Flowering Plants. New York, New York: New York Botanical Garden Press. ISBN 978-0893273323.
2. ^ Carlquist, S.; E.L. Schneider (2002). "The tracheid–vessel element transition in angiosperms involves multiple independent features: cladistic consequences" 89: 185-195.
3. ^ Cronquist, A. (Aug 1988.). The Evolution and Classification of Flowering Plants. New York, New York: New York Botanical Garden Press. ISBN 978-0893273323.
- Campbell, Neil A.; Jane B. Reece (2002). Biology, 6th ed., Benjamin Cummings. ISBN 978-0805366242.
- Kenrick, Paul; Crane, Peter R. (1997). The Origin and Early Diversification of Land Plants: A Cladistic Study. Washington, D. C.: Smithsonian Institution Press. ISBN 1-56098-730-8.
- Muhammad, A.F.; R. Sattler (1982). "Vessel Structure of Gnetum and the Origin of Angiosperms". American Journal of Botany 69: 1004-21.
- Melvin T. Tyree; Martin H. Zimmermann (2003). Xylem Structure and the Ascent of Sap, 2nd ed., Springer. ISBN 3-540-43354-6. recent update of the classic book on xylem transport by the late Martin Zimmermann
Divisions
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- Non-seed-bearing plants
- †Rhyniophyta
- †Zosterophyllophyta
- Lycopodiophyta
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In vascular plants, phloem is the living tissue that carries organic nutrients, particularly sucrose, a sugar, to all parts of the plant where needed. In trees, the phloem is the innermost layer of the bark, hence the name, derived from the Greek word
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Transpirational pull is the main phenomenon driving the flow of water in the xylem tissues of large plants.
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Mechanisms
Transpirational pull results ultimately from the evaporation of water from the surfaces of cells in the interior of the leaves...... Click the link for more information.
Evaporation is the process by which molecules in a liquid state (e.g. water) spontaneously become gaseous (e.g. water vapor), without being heated to boiling point. It is the opposite of condensation.
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Water is a common chemical substance that is essential to all known forms of life.[1] In typical usage, water refers only to its liquid form or state, but the substance also has a solid state, ice, and a gaseous state, water vapor.
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Transpiration is the evaporation of water from the aerial parts of plants, especially leaves but also stems, flowers and roots. Leaf transpiration occurs through stomata, and can be thought of as a necessary "cost" associated with the opening of stomata to allow the diffusion of
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A: The bottom of a concave meniscus.
B: The top of a convex meniscus.]] Meniscus, plural: menisci, from the Greek for "crescent", is a curve in the surface of a liquid and is produced in response to the surface of the container or another
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B: The top of a convex meniscus.]] Meniscus, plural: menisci, from the Greek for "crescent", is a curve in the surface of a liquid and is produced in response to the surface of the container or another
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Surface tension is an effect within the surface layer of a liquid that causes that layer to behave as an elastic sheet. It allows insects, such as the water strider (pond skater, UK), to walk on water.
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Root pressure occurs in the xylem of some vascular plants when the soil moisture level is high either at night or when transpiration is low during the day. When transpiration is high, xylem sap is usually under tension, rather than under pressure, due to transpirational pull.
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Water potential is the potential energy of water relative to pure water in reference conditions. It quantifies the tendency of water to move from one area to another due to osmosis, gravity, mechanical pressure, or capillary action.
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This article is about chemical solutions. For other uses, see Solution (disambiguation).
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Osmosis is the net movement of water across a partially permeable membrane from a region of high solvent potential to an area of low solvent potential, up a solute concentration gradient.
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A hydathode is a type of tissue in leaves, usually more advanced plant species, that permits the release of water through pores in the epidermis or margin of leaves. They probably evolved from modified stomata.
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Guttation is the appearance of drops of xylem sap on the tips or edges of leaves of some vascular plants, such as grasses.
At night, transpiration usually does not occur because most plants have their stomata closed.
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At night, transpiration usually does not occur because most plants have their stomata closed.
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V. riparia
Binomial name
Vitis riparia
Vitis riparia Michx, also commonly known as River Bank Grape or Frost Grape
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Binomial name
Vitis riparia
Vitis riparia Michx, also commonly known as River Bank Grape or Frost Grape
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vascular bundle is a part of the transport system in vascular plants. The transport itself happens in vascular tissue, which exists in two forms: xylem and phloem. Both these tissues are present in a vascular bundle, which in addition will include supporting and protective tissues.
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In vascular plants, xylem is one of the two types of transport tissue, phloem being the other one. The word "xylem" is derived from classical Greek ξυλον (xylon
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A meristem is a tissue in all plants consisting of undifferentiated cells (meristematic cells) and found in zones of the plant where growth can take place.
Differentiated plant cells generally cannot divide or produce cells of a different type.
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Differentiated plant cells generally cannot divide or produce cells of a different type.
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The vascular cambium is a lateral meristem: The vascular cambium is the source of both the secondary xylem (inwards, towards the pith) and the secondary phloem (outwards), and is located between these tissues in the stem and root. A few leaves even have a vascular cambium.
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In a vascular plant, the stele is the central part of the root or stem containing the vascular tissue and occasionally a pith. The concept of the stele was developed in the late nineteenth century by French botanists P. E. L. van Tieghem and H.
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Tracheids are elongated cells in the xylem of vascular plants, serving in the transport of water. The build of tracheids will vary according to where they occur.
Tracheids are one of two types of tracheary elements, vessel elements being the other.
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Tracheids are one of two types of tracheary elements, vessel elements being the other.
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vessel element is one of the cell types found in xylem, the water conducting tissue of plants. Vessel elements are typically found in the angiosperms but absent from most gymnosperms such as the conifers.
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A meristem is a tissue in all plants consisting of undifferentiated cells (meristematic cells) and found in zones of the plant where growth can take place.
Differentiated plant cells generally cannot divide or produce cells of a different type.
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Differentiated plant cells generally cannot divide or produce cells of a different type.
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The vascular cambium is a lateral meristem: The vascular cambium is the source of both the secondary xylem (inwards, towards the pith) and the secondary phloem (outwards), and is located between these tissues in the stem and root. A few leaves even have a vascular cambium.
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gymnosperms (Gymnospermae) are a group of spermatophyte seed-bearing plants with ovules on the edge or blade of an open sporophyll, the sporophylls usually arranged in cone-like structures.
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