Stele (biology)

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In a vascular plant, the stele is the central part of the root or stem [1] containing the tissues derived from the procambium. These include vascular tissue, in some cases ground tissue (pith) and a pericycle, which, if present, defines the outermost boundary of the stele. Outside the stele lies the endodermis, which is the innermost cell layer of the cortex.

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The concept of the stele was developed in the late 19th century by French botanists P. E. L. van Tieghem and H. Doultion as a model for understanding the relationship between the shoot and root, and for discussing the evolution of vascular plant morphology. [2] Now, at the beginning of the 21st century, plant molecular biologists are coming to understand the genetics and developmental pathways that govern tissue patterns in the stele.[ citation needed ] Moreover, physiologists are examining how the anatomy (sizes and shapes) of different steles affect the function of organs.

Protostele

Three basic types of protostele Protostele.jpg
Three basic types of protostele

The earliest vascular plants had stems with a central core of vascular tissue. [3] [4] This consisted of a cylindrical strand of xylem, surrounded by a region of phloem. Around the vascular tissue there might have been an endodermis that regulated the flow of water into and out of the vascular system. Such an arrangement is termed a protostele. [5]

There are usually three basic types of protostele:

Siphonostele

Three basic types of siphonostele Siphonostele.jpg
Three basic types of siphonostele

Siphonosteles have a region of ground tissue called the pith internal to xylem. The vascular strand comprises a cylinder surrounding the pith. Siphonosteles often have interruptions in the vascular strand where leaves (typically megaphylls) originate (called leaf gaps).

Siphonosteles can be ectophloic (phloem present only external to the xylem) or they can be amphiphloic (with phloem both external and internal to the xylem). Among living plants, many ferns and some Asterid flowering plants have an amphiphloic stele.

An amphiphloic siphonostele can be called a:

Most seed plant stems possess a vascular arrangement which has been interpreted as a derived siphonostele, and is called a

There is also a variant of the eustele found in monocots like maize and rye. The variation has numerous scattered bundles in the stem and is called an atactostele (characterestic of monocot stem). However, it is really just a variant of the eustele. [7] [8]

See also

Citations

  1. Foster & Gifford (1974), p. 58.
  2. Gifford & Foster (1988), p. 42.
  3. Bold, Alexopoulos & Delevoryas (1987), p. 320.
  4. Stewart & Rothwell (1993), pp. 85–89.
  5. Gifford & Foster (1988), p. 44.
  6. Arnold (1947), pp. 66–68.
  7. 1 2 Bold, Alexopoulos & Delevoryas (1987), p. 322.
  8. Gifford & Foster (1988), p. 45.

Related Research Articles

Xylem Water transport tissue in vascular plants

Xylem is one of the two types of transport tissue in vascular plants, the other being phloem. The basic function of xylem is to transport water from roots to stems and leaves, but it also transports nutrients. The word "xylem" is derived from the Greek word ξύλον (xylon), meaning "wood"; the best-known xylem tissue is wood, though it is found throughout a plant. The term was introduced by Carl Nägeli in 1858.

Phloem Sugar transport tissue in vascular plants

Phloem is the living tissue in vascular plants that transports the soluble organic compounds made during photosynthesis and known as photosynthates, in particular the sugar sucrose, to parts of the plant where needed. This transport process is called translocation. In trees, the phloem is the innermost layer of the bark, hence the name, derived from the Greek word φλοιός (phloios) meaning "bark". The term was introduced by Carl Nägeli in 1858.

Vascular plant Clade of land plants with xylem and phloem

Vascular plants, also known as Tracheophyta, form a large group of plants that are defined as land plants with lignified tissues for conducting water and minerals throughout the plant. They also have a specialized non-lignified tissue to conduct products of photosynthesis. Vascular plants include the clubmosses, horsetails, ferns, gymnosperms and angiosperms. Scientific names for the group include Tracheophyta, Tracheobionta and Equisetopsida sensu lato. Some early land plants had less developed vascular tissue; the term eutracheophyte has been used for all other vascular plants.

Tissue (biology) Level of cellular organization

In biology, tissue is a cellular organizational level between cells and a complete organ. A tissue is an ensemble of similar cells and their extracellular matrix from the same origin that together carry out a specific function. Organs are then formed by the functional grouping together of multiple tissues.

<i>Psilotum</i> Genus of ferns in the family Psilotaceae

Psilotum is a genus of fern-like vascular plants, commonly known as whisk ferns. It is one of two genera in the family Psilotaceae, the other being Tmesipteris. Plants in these two genera were once thought to be descended from the earliest surviving vascular plants, but more recent phylogenies place them as basal ferns, as a sister group to Ophioglossales. They lack true roots and leaves are very reduced, the stems being the organs containing conducting tissue. There are only two species in Psilotum and a hybrid between the two. They differ from those in Tmesipteris in having stems with many branches and a synangium with three lobes rather than two.

Vascular cambium Main growth tissue in the stems, roots of plants

The vascular cambium is the main growth tissue in the stems and roots of many plants, specifically in dicots such as buttercups and oak trees, gymnosperms such as pine trees, as well as in certain vascular plants. It produces secondary xylem inwards, towards the pith, and secondary phloem outwards, towards the bark.

In plant anatomy and evolution a microphyll is a type of plant leaf with one single, unbranched leaf vein. Plants with microphyll leaves occur early in the fossil record, and few such plants exist today. In the classical concept of a microphyll, the leaf vein emerges from the protostele without leaving a leaf gap. Leaf gaps are small areas above the node of some leaves where there is no vascular tissue, as it has all been diverted to the leaf. Megaphylls, in contrast, have multiple veins within the leaf and leaf gaps above them in the stem.

Endodermis Inner layer of cortex in vascular plant roots

The endodermis is the central, innermost layer of cortex in land plants. It is a cylinder of compact living cells, the radial walls of which are impregnated with hydrophobic substances to restrict apoplastic flow of water to the inside. The endodermis is the boundary between the cortex and the stele.

<i>Calamites</i> Extinct genus of vascular plants in the Order Equisetales

Calamites is a genus of extinct arborescent (tree-like) horsetails to which the modern horsetails are closely related. Unlike their herbaceous modern cousins, these plants were medium-sized trees, growing to heights of 30-50 meters. They were components of the understories of coal swamps of the Carboniferous Period.

Equisetidae Subclass of ferns

Equisetidae is one of the four subclasses of Polypodiopsida (ferns), a group of vascular plants with a fossil record going back to the Devonian. They are commonly known as horsetails. They typically grow in wet areas, with whorls of needle-like branches radiating at regular intervals from a single vertical stem.

The pericycle is a cylinder of parenchyma or sclerenchyma cells that lies just inside the endodermis and is the outer most part of the stele of plants.

Ground tissue Various non-vascular tissues in plants

The ground tissue of plants includes all tissues that are neither dermal nor vascular. It can be divided into three types based on the nature of the cell walls.

  1. Parenchyma cells have thin primary walls and usually remain alive after they become mature. Parenchyma forms the "filler" tissue in the soft parts of plants, and is usually present in cortex, pericycle, pith, and medullary rays in primary stem and root.
  2. Collenchyma cells have thin primary walls with some areas of secondary thickening. Collenchyma provides extra mechanical and structural support, particularly in regions of new growth.
  3. Sclerenchyma cells have thick lignified secondary walls and often die when mature. Sclerenchyma provides the main structural support to a plant.
Vascular bundle Longitudinal strand of vascular tissue in the roots, stems and leaves of higher plants

A vascular bundle is a part of the transport system in vascular plants. The transport itself happens in the stem, 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. In addition, there is also a tissue between xylem and phloem which is the cambium.

Vascular tissue Conducting tissue in vascular plants

Vascular tissue is a complex conducting tissue, formed of more than one cell type, found in vascular plants. The primary components of vascular tissue are the xylem and phloem. These two tissues transport fluid and nutrients internally. There are also two meristems associated with vascular tissue: the vascular cambium and the cork cambium. All the vascular tissues within a particular plant together constitute the vascular tissue system of that plant.

Secondary growth

In botany, secondary growth is the growth that results from cell division in the cambia or lateral meristems and that causes the stems and roots to thicken, while primary growth is growth that occurs as a result of cell division at the tips of stems and roots, causing them to elongate, and gives rise to primary tissue. Secondary growth occurs in most seed plants, but monocots usually lack secondary growth. If they do have secondary growth, it differs from the typical pattern of other seed plants.

Lepidodendrales Extinct order of vascular tree-like plants

Lepidodendrales were primitive, vascular, arborescent (tree-like) plants related to the lycopsids. Members of Lepidodendrales are the best understood of the fossil lycopsids due to the vast diversity of Lepidodendrales specimens and the diversity in which they were preserved; the extensive distribution of Lepidodendrales specimens as well as their well-preservedness lends paleobotanists exceptionally detailed knowledge of the coal-swamp giants’ reproductive biology, vegetative development, and role in their paleoecosystem. The defining characteristics of the Lepidodendrales are their secondary xylem, extensive periderm development, three-zoned cortex, rootlike appendages known as stigmarian rootlets arranged in a spiralling pattern, and megasporangium each containing a single functional megaspore that germinates inside the sporangium. Many of these different plant organs have been assigned both generic and specific names as relatively few have been found organically attached to each other. Some specimens have been discovered which indicate heights of 40 and even 50 meters and diameters of over 2 meters at the base. The massive trunks of some species branched profusely, producing large crowns of leafy twigs; though some leaves were up to 1 meter long, most were much shorter, and when leaves dropped from branches their conspicuous leaf bases remained on the surface of branches. Strobili could be found at the tips of distal branches or in an area at the top of the main trunk. The underground organs of Lepidodendrales typically consisted of dichotomizing axes bearing helically arranged, lateral appendages serving an equivalent function to roots. Sometimes called "giant club mosses", they are in fact more closely related to quillworts than to club mosses.

Woody plant Plant that produces wood and has a hard stem

A woody plant is a plant that produces wood as its structural tissue and thus has a hard stem. In cold climates, woody plants further survive winter or dry season above ground, as opposite to herbaceous plants that die back to the ground until spring.

Plant stem structural axis of a vascular plant

A stem is one of two main structural axes of a vascular plant, the other being the root. It supports leaves, flowers and fruits, transports water and dissolved substances between the roots and the shoots in the xylem and phloem, stores nutrients, and produces new living tissue.

Tetraxylopteris is a genus of extinct vascular plants of the Middle to Upper Devonian. Fossils were first found in New York State, USA. A second species was later found in Venezuela.

Rotafolia songziensis is a species of the extinct Sphenophyllales horsetails.

References