Ground tissue
From Wikipedia, the free encyclopedia
1. Pith,
2. Protoxylem,
3. Xylem I,
4. Phloem I,
5. Sclerenchyma (bast fibre),
6. Cortex,
7. Epidermis
The types of ground tissue found in plants develop from ground tissue meristem and consists of three simple tissues:
- Parenchyma (have retained their protoplasm)
- Collenchyma (have retained their protoplasm)
- Sclerenchyma (have lost their protoplasm in mature stage, i.e. are 'dead')
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[edit] Parenchyma
Parenchyma is the most common and versatile ground tissue. It forms, for example, the cortex and pith of stems, the cortex of roots, the mesophyll of leaves, the pulp of fruits, and the endosperm of seeds. Parenchyma cells are living cells and may remain meristematic at maturity, meaning that they are capable of cell division. They have thin but flexible cell walls, and are generally polygonal when close-packed, but approximately spherical when isolated from their neighbours. They have large central vacuoles, which allows the cells to store and regulate ions, waste products and water.
Parenchyma cells have a variety of functions:
- In leaves, they form the mesophyll and are responsible for photosynthesis and the exchange of gases[1].
- Storage
- Secretion (e.g. Epithelial cells lining the inside of resin ducts)
- Healing
- Other specialized functions
The form of parenchyma cells varies with their function. The epidermal parenchyma cells of a leaf are barrel shaped in cross section, but have a variety of outline shapes ranging from simple polygons to strongly branched and interlocked shapes resembling the pieces of a jigsaw Puzzle, as in the leaves if Arabidopsis thaliana. In the epidermis of higher plants, only the guard cells have chloroplasts. This tissue serves as a barrier wall and protects the internal tissues from injury[1]. In the spongy mesophyll of a leaf, parenchyma cells range from near-spherical and loosely arranged with large intercellular spaces[1] to branched or stellate, mutally interconnected with their neighbours at the ends of the arms to form a three-dimensional network, as in the red kidney bean Phaseolus vulgaris and other mesophytes[2] These cells, with the epidermal guard cells of the stoma, form a system of air spaces and chambers that regulate the exchange of gases[1].
[edit] Collenchyma
Collenchyma tissue is composed of elongated cells with unevenly thickened walls. They provide structural support, particularly in growing shoots and leaves. Collenchyma tissue composes, for example, the resilient strands in stalks of celery. Its growth is strongly affected by mechanical stress upon the plant. The walls of collenchyma in shaken plants (to mimic the effects of wind etc), may be 40%-100% thicker than those not shaken. The name collenchyma derives from the Greek word "kolla", meaning "glue", which refers to the thick, glistening appearance of the walls in fresh tissues.
There are three principal types of collenchyma:
- Angular collenchyma (thickened at intercellular contact points)
- Tangential collenchyma (cells arranged into ordered rows and thickened at the tangential face of the cell wall)
- Lacunar collenchyma (have intercellular space and thickening proximal to the intercellular space)
[edit] Sclerenchyma
Sclerenchyma is a supporting tissue. Two groups of sclerenchyma cells exist: fibres and sclereids. Their walls consist of cellulose and lignin. Sclerenchyma cells are the principal supporting cells in plant tissues that have ceased elongation. Sclerenchyma fibres are of great economical importance, since they constitute the source material for many fabrics (flax, hemp, jute, ramie).
Unlike the collenchyma, mature sclerenchyma is composed of dead cells with extremely thick cell walls (secondary walls) that make up to 90% of the whole cell volume. The term "sclerenchyma" is derived from the Greek "scleros", meaning "hard". It is their hard, thick walls that make sclerenchyma cells important strengthening and supporting elements in plant parts that have ceased elongation. The difference between fibres and sclereids is not always clear. Transitions do exist, sometimes even within one and the same plant.
Fibres are generally long, slender, so-called prosenchymatous cells, usually occurring in strands or bundles. Such bundles or the totality of a stem's bundles are colloquially called fibres. Their high load-bearing capacity and the ease with which they can be processed has since antiquity made them the source material for a number of things, like ropes, fabrics or mattresses. The fibres of flax (Linum usitatissimum) have been known in Europe and Egypt for more than 3000 years, those of hemp (Cannabis sativa) in China for just as long. These fibres, and those of jute (Corchorus capsularis) and ramie (Boehmeria nivea, a nettle), are extremely soft and elastic and are especially well suited for the processing to textiles. Their principal cell wall material is cellulose.
Contrasting are hard fibres that are mostly found in monocots. Typical examples are the fibres of many Gramineae, Agaves (sisal: Agave sisalana), lilies (Yucca or Phormium tenax), Musa textilis and others. Their cell walls harbour, besides cellulose, a high proportion of lignin. The load-bearing capacity of Phormium tenax is as high as 20-25 kg/mm2, the same as that of good steel wire (25 kg/ mm2), but the fibre tears as soon as too great a strain is placed upon it, while the wire distorts and tears not before a strain of 80 kg/mm2. The thickening of a cell wall has been studied in Linum. Starting at the centre of the fibre are the thickening layers of the secondary wall deposited one after the other. Growth at both tips of the cell leads to simultaneous elongation. During development the layers of secondary material seem like tubes, of which the outer one is always longer and older than the next. After completion of growth the missing parts are supplemented, so that the wall is evenly thickened up to the tips of the fibres.
Fibres stem usually form meristematic tissues. Cambium and procambium are their main centers of production. They are often associated with the xylem of the vascular bundles. The fibres of the xylem are always lignified. Reliable evidence for the fibre cells' evolutionary origin from tracheids exists. During evolution the strength of the tracheid cell walls was enhanced, the ability to conduct water was lost and the size of the pits reduced. Fibres that do not belong to the xylem are bast (outside the ring of cambium) and such fibres that are arranged in characteristic patterns at different sites of the shoot.
Sclereids are small bundles of sclerenchyma tissue in plants that form durable layers, such as the cores of apples and the gritty texture of pears. Sclereids are variable in shape. The cells can be isodiametric, prosenchymatic, forked or fantastically 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. But compared with most fibres, sclereids are relatively short. Characteristic examples are the stone cells (called stone cells because of their hardness) of pears (Pyrus communis) and quinces (Cydonia oblonga) and those of the shoot of the wax-plant (Hoya carnosa). The cell walls fill nearly all the cell's volume. A layering of the walls and the existence of branched pits is clearly visible. Branched pits such as these are called ramiform pits. The shell of many seeds like those of nuts as well as the stones of drupes like cherries or plums are made up from sclereids.
[edit] References
- Moore, Randy; Clark, W. Dennis; and Vodopich, Darrell S. (1998). Botany (3rd ed.). McGraw-Hill. ISBN 0-697-28623-1.
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