Sclereid

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Fresh mount of a sclereid in a banana fruit Komorka kamienna w bananie.jpg
Fresh mount of a sclereid in a banana fruit

Sclereids are a reduced form of sclerenchyma cells with highly thickened, lignified cellular walls that form small bundles of durable layers of tissue in most plants. [1] The presence of numerous sclereids form the cores of apples and produce the gritty texture of guavas.

Contents

Although sclereids are variable in shape, the cells are generally isodiametric, prosenchymatic, forked, or elaborately branched. They can be grouped into bundles, can form complete tubes located at the periphery, or can occur as single cells or small groups of cells within parenchyma tissues. An isolated sclereid cell is known as an idioblast. Sclereids are typically found in the epidermis, ground tissue, and vascular tissue. [2]

The term "sclereid" was introduced by Alexander Tschirch in 1885. [3]

Origin

Sclereids are created through belated sclerosis of parenchyma cells or can arise from sclereid primordia that are individualized early in development. Sclerification typically involves thickening of the cell wall, increasing rigidity. In the phloem, when tissue ceases to function in conduction cells may begin sclerification. In vascular tissue, sclereids will develop from cambial and procambial cells. [4]

Stem sclereids

In the vascular region of the stem of Hoya carnosa , a column of sclereids can be found, and in the pith of stems of Hoya and Podocarpus groups of sclereids can be found. These are sclereids with thick cell walls and numerous pits, resembling adjacent parenchyma cells. This resemblance suggests that these sclereids are originally parenchyma cells, but are so sclerified that they are now sclereid cells rather than parenchyma cells. These sclereids are an example of brachysclereids, or stone cells. [2]

Leaf sclereids

Long tapered sclereids supporting a leaf edge in Dionysia kossinskyi Dionysia kossinskyi sclereids.TIF
Long tapered sclereids supporting a leaf edge in Dionysia kossinskyi

Leaves contain a variety of types of sclereids. In the mesophyll, two distinct sclereid structures are found. Sclereids in a diffuse pattern are dispersed throughout the leaf tissue, and sclereids in a terminal pattern are concentrated about the tips of leaf veins. Sclereid formations in leaves include the branched sclereids of Trochodendron , the columnar sclereids of Hakea , and the hair-like trichosclereids that branch into air chambers within the leaves of the water lily and yellow pond lily. Sclereids can also form part of or the entire epidermis of foliar structures such as the clove scales of Allium sativum . [2]

Especially interesting are the sclereids in olive leaves. They are typically 1 mm (0.039 in) in length and are thus named fiberlike sclereids. These sclereids permeate the mesophyll as a dense mat. [5] During sclerification these fiberlike sclereid cells can increase by several hundred times their original size, compared to other parenchyma cells that only increase by two or three times. [4]

Fruit sclereids

Sclereids in fruits vary in form and use. In pears, sclereids from concentric clusters that grow about earlier formed sclereids. These pear sclereids, as well as sclereids within quince fruit, often form bordered pits when the cell wall increases in thickness during sclerification. In apples, layers of elongated sclereids form the endocarp that encloses the seeds. [2]

Seed sclereids

The hardening of seed coats during ripening often occurs through sclerification, when the secondary cell walls are thickened in the epidermis and below the epidermis. Leguminous seeds are examples of such sclerification. Larger sclereids form columns in the epidermis of pea, bean, and soybean seeds, and bone-shaped osteosclereids occur beneath the epidermis. In the seedcoats of coconuts, sclereids possess numerous bordered pits. [2] These larger macrosclereids found in seedcoats are of protodermal origin. [4]

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Plant cells are eukaryotic cells present in green plants, photosynthetic eukaryotes of the kingdom Plantae. Their distinctive features include primary cell walls containing cellulose, hemicelluloses and pectin, the presence of plastids with the capability to perform photosynthesis and store starch, a large vacuole that regulates turgor pressure, the absence of flagella or centrioles, except in the gametes, and a unique method of cell division involving the formation of a cell plate or phragmoplast that separates the new daughter cells.

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 Ancient 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 Ancient Greek word φλοιός (phloiós), meaning "bark". The term was introduced by Carl Nägeli in 1858.

Vascular plant Clade of land plants with xylem and phloem

Vascular plants, also called tracheophytes or collectively Tracheophyta, form a large group of land plants that have 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, including all living ones.

Tissue (biology) A group of cells having similar appearance and performing the same function is known as a tissue .

In biology, tissue is a biological 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.

Bark (botany) Outermost layers of stems and roots of woody plants

Bark is the outermost layers of stems and roots of woody plants. Plants with bark include trees, woody vines, and shrubs. Bark refers to all the tissues outside the vascular cambium and is a nontechnical term. It overlays the wood and consists of the inner bark and the outer bark. The inner bark, which in older stems is living tissue, includes the innermost layer of the periderm. The outer bark on older stems includes the dead tissue on the surface of the stems, along with parts of the outermost periderm and all the tissues on the outer side of the periderm. The outer bark on trees which lies external to the living periderm is also called the rhytidome.

Lenticel Tissue that allows gas exchange in plant organs

A lenticel is a porous tissue consisting of cells with large intercellular spaces in the periderm of the secondarily thickened organs and the bark of woody stems and roots of dicotyledonous flowering plants. It functions as a pore, providing a pathway for the direct exchange of gases between the internal tissues and atmosphere through the bark, which is otherwise impermeable to gases. The name lenticel, pronounced with an, derives from its lenticular (lens-like) shape. The shape of lenticels is one of the characteristics used for tree identification.

Cortex (botany)

A cortex is an outer layer of a stem or root in a plant, lying below the epidermis but outside of the vascular bundles. It is also the surface layer or "skin" of the nonfruiting part of the body of some lichens.

Sieve elements are specialized cells that are important for the function of phloem, which is a highly organized tissue that transports organic compounds made during photosynthesis. Sieve elements are the major conducting cells in phloem. Conducting cells aid in transport of molecules especially for long-distance signaling. In plant anatomy, there are two main types of sieve elements. Companion cells and sieve cells originate from meristems, which are tissues that actively divide throughout a plant's lifetime. They are similar to the development of xylem, a water conducting tissue in plants whose main function is also transportation in the plant vascular system. Sieve elements' major function includes transporting sugars over long distance through plants by acting as a channel. Sieve elements elongate cells containing sieve areas on their walls. Pores on sieve areas allow for cytoplasmic connections to neighboring cells, which allows for the movement of photosynthetic material and other organic molecules necessary for tissue function. Structurally, they are elongated and parallel to the organ or tissue that they are located in. Sieve elements typically lack a nucleus and contain none to a very small number of ribosomes. The two types of sieve elements, sieve tube members and sieve cells, have different structures. Sieve tube members are shorter and wider with greater area for nutrient transport while sieve cells tend to be longer and narrower with smaller area for nutrient transport. Although the function of both of these kinds of sieve elements is the same, sieve cells are found in gymnosperms, non-flowering vascular plants, while sieve tube members are found in angiosperms, flowering vascular 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.

Epidermis (botany) Layer of cells that covers leaves, flowers, roots of plants

The epidermis is a single layer of cells that covers the leaves, flowers, roots and stems of plants. It forms a boundary between the plant and the external environment. The epidermis serves several functions: it protects against water loss, regulate gas exchange, secretes metabolic compounds, and absorbs water and mineral nutrients. The epidermis of most leaves shows dorsoventral anatomy: the upper (adaxial) and lower (abaxial) surfaces have somewhat different construction and may serve different functions. Woody stems and some other stem structures such as potato tubers produce a secondary covering called the periderm that replaces the epidermis as the protective covering.

Hydathode Water-secreting gland in plant leaf margins

A hydathode is a type of pore, commonly found in angiosperms, that secretes water through pores in the epidermis or leaf margin, typically at the tip of a marginal tooth or serration. Hydathodes occur in the leaves of submerged aquatic plants such as Ranunculus fluitans as well as herbaceous plants of drier habitats such as Campanula rotundifolia. They are connected to the plant vascular system by a vascular bundle. Hydathodes are commonly seen in water lettuce, water hyacinth, rose, balsam, and many other species.

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 Type of growth in plants

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.

Aerenchyma

Aerenchyma or aeriferous parenchyma is a modification of the parenchyma to form a spongy tissue that creates spaces or air channels in the leaves, stems and roots of some plants, which allows exchange of gases between the shoot and the root. The channels of air-filled cavities provide a low-resistance internal pathway for the exchange of gases such as oxygen and ethylene between the plant above the water and the submerged tissues. Aerenchyma is also widespread in aquatic and wetland plants which must grow in hypoxic soils.

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 believed to be more closely related to extant quillworts based on xylem, although fossil specimens of extinct Selaginellales from the Late Carboniferous also had secondary xylem.

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.

Leaf Photosynthetic part of a vascular plant

A leaf is the principal lateral appendage of the vascular plant stem, usually borne above ground and specialized for photosynthesis. The leaves, stem, flower and fruit together form the shoot system. Leaves are collectively referred to as foliage, as in "autumn foliage". In most leaves, the primary photosynthetic tissue, the palisade mesophyll, is located on the upper side of the blade or lamina of the leaf but in some species, including the mature foliage of Eucalyptus, palisade mesophyll is present on both sides and the leaves are said to be isobilateral. Most leaves are flattened and have distinct upper and lower surfaces that differ in color, hairiness, the number of stomata, the amount and structure of epicuticular wax and other features. Leaves are mostly green in color due to the presence of a compound called chlorophyll that is essential for photosynthesis as it absorbs light energy from the sun. A leaf with lighter-colored or white patches or edges is called a variegated leaf.

Idioblast

An idioblast is an isolated plant cell that differs from neighboring tissues. They have various functions such as storage of reserves, excretory materials, pigments, and minerals. They could contain oil, latex, gum, resin, tannin or pigments etc. Some can contain mineral crystals such as acrid tasting and poisonous calcium oxalate or carbonate or silica. Any of the tissue or tissue systems of plants can contain idioblasts. Idioblasts are divided into three main categories: excretory, tracheoid, and sclerenchymatous.

References

  1. Evert, Ray F; Eichhorn, Susan E. Esau's Plant Anatomy: Meristems, Cells, and Tissues of the Plant Body: Their Structure, Function, and Development. Publisher: Wiley-Liss 2006. ISBN   978-0471738435
  2. 1 2 3 4 5 Katherine Easu (1977). Anatomy of Seed Plants. Plant Anatomy (2nd ed.). John Wiley & Sons. p. 72. ISBN   0-471-24520-8.
  3. Tschirch, A. (1885). Beiträge zur Kenntnis des mechanischen Gewebesystems der Pflanzen. Pringsheims Jahrbücher für Wissenschaftliche Botanik XVI: 303-335.
  4. 1 2 3 S. R. Mishra (2009). Understanding Plant Anatomy. Discovery Publishing House. p. 105. ISBN   9788183564571.
  5. S. M. Reddy, S. J. Chary (2003). Gymnosperms, Plant Anatomy, Genetics, Ecology. University Botany. Vol. 2. New Age International. p. 105. ISBN   9788122414776.

Further reading