Pit (botany)

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Bordered pits in the wood of Picea abies. The top section is a cross-sectional view with bordered pits shown between adjacent cells, and the bottom section is a radial view with numerous bordered pits shown. Tracheiden Picea abies.jpg
Bordered pits in the wood of Picea abies . The top section is a cross-sectional view with bordered pits shown between adjacent cells, and the bottom section is a radial view with numerous bordered pits shown.

Pits are relatively thinner portions of the cell wall that adjacent cells can communicate or exchange fluid through. Pits are characteristic of cell walls with secondary layers. Generally each pit has a complementary pit opposite of it in the neighboring cell. These complementary pits are called "pit pairs". [1]

Contents

Pits are composed of three parts: the pit chamber, the pit aperture, and the pit membrane. The pit chamber is the hollow area where the secondary layers of the cell wall are absent. The pit aperture is the opening at either end of the pit chamber. The pit membrane is the primary cell wall and middle lamella, or the membrane between adjacent cell walls, at the middle of the pit chamber. [2]

The primary cell wall at the pit membrane may also have depressions similar to the pit depressions of the secondary layers. These depressions are primary pit-fields, or primary pits. In the primary pit, the primordial pit provides an interruption in the primary cell wall that the plasmodesmata can cross. The primordial pit is the only aperture in the otherwise continuous primary cell wall. [3]

Pit pairs are a characteristic feature of xylem, as sap flows through the pits of xylem cells. [4]

Types of pits

A simplified diagram of a simple pit pair Simple Pit Pair.jpg
A simplified diagram of a simple pit pair

Though pits are usually simple and complementary, a few more pit variations can be formed: [5]

Plasmodesmata

Plasmodesmata are thin sections of the endoplasmic reticulum that traverse pits and connect adjacent cells. These sections provide an avenue of transport through the pits and facilitate communication. [6] Plasmodesmata are not restricted to pits however, as plasmodesmata often cross a cell wall of constant width and occasionally the cell wall is even wider in areas where plasmodesmata traverse it. [3]

Torus and margo

A simplified diagram of a bordered pit-pair with a torus and margo. The top shows an unobstructed pit and the bottom shows an aspirated pit, with the margo flexing under stress. Torus and Margo.png
A simplified diagram of a bordered pit-pair with a torus and margo. The top shows an unobstructed pit and the bottom shows an aspirated pit, with the margo flexing under stress.

The torus and margo are characteristic features of bordered pit-pairs in gymnosperms, such as Coniferales, Ginkgo , and Gnetales . In other vascular plants, the torus is rare. The pit membrane is separated into two parts: a thick impermeable torus at the center of the pit membrane, and the permeable margo surrounding it. The torus regulates the functions of the bordered pit, and the margo is a cell wall-derived porous membrane that supports the torus. The margo is composed of bundles of microfibrils that radiate from the torus. [3]

The margo is flexible and can move towards either side of the pit while under stress. This allows the thick, impermeable torus to block the pit aperture. When the torus is displaced so that it blocks the pit aperture, the pit is said to be aspirated. [7]

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<span class="mw-page-title-main">Cell wall</span> Outermost layer of some cells

A cell wall is a structural layer surrounding some types of cells, just outside the cell membrane. It can be tough, flexible, and sometimes rigid. It provides the cell with both structural support and protection, and also acts as a filtering mechanism. Cell walls are absent in many eukaryotes, including animals, but are present in some other ones like fungi, algae and plants, and in most prokaryotes. A major function is to act as pressure vessels, preventing over-expansion of the cell when water enters.

<span class="mw-page-title-main">Plant cell</span> Type of eukaryotic cell present in green plants

Plant cells are the 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.

<span class="mw-page-title-main">Xylem</span> 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.

<span class="mw-page-title-main">Phloem</span> 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 the rest of the plant. 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.

<span class="mw-page-title-main">Tissue (biology)</span> Group of cells having similar appearance and performing the same function

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<span class="mw-page-title-main">Root pressure</span> Transverse osmotic pressure within the cells of a root system

Root pressure is the transverse osmotic pressure within the cells of a root system that causes sap to rise through a plant stem to the leaves.

<span class="mw-page-title-main">Epithelium</span> Tissue lining the surfaces of organs in animals

Epithelium or epithelial tissue is a thin, continuous, protective layer of compactly packed cells with a little intercellular matrix. Epithelial tissues line the outer surfaces of organs and blood vessels throughout the body, as well as the inner surfaces of cavities in many internal organs. An example is the epidermis, the outermost layer of the skin. Epithelial tissue is one of the four basic types of animal tissue, along with connective tissue, muscle tissue and nervous tissue. These tissues also lack blood or lymph supply. The tissue is supplied by nerves.

<span class="mw-page-title-main">Pith</span> Plant tissue

Pith, or medulla, is a tissue in the stems of vascular plants. Pith is composed of soft, spongy parenchyma cells, which in some cases can store starch. In eudicotyledons, pith is located in the center of the stem. In monocotyledons, it extends also into flowering stems and roots. The pith is encircled by a ring of xylem; the xylem, in turn, is encircled by a ring of phloem.

A tracheid is a long and tapered lignified cell in the xylem of vascular plants. It is a type of conductive cell called a tracheary element. Angiosperms use another type of conductive cell, called vessel elements, to transport water through the xylem. The main functions of tracheid cells are to transport water and inorganic salts, and to provide structural support for trees. There are often pits on the cell walls of tracheids, which allows for water flow between cells. Tracheids are dead at functional maturity and do not have a protoplast. The wood (softwood) of gymnosperms such as pines and other conifers is mainly composed of tracheids. Tracheids are also the main conductive cells in the primary xylem of ferns.

<span class="mw-page-title-main">Endodermis</span> Inner layer of cortex in vascular plant roots

The endodermis is the 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.

<span class="mw-page-title-main">Sap</span> Fluid transported in xylem cells or phloem sieve tube elements of a plant

Sap is a fluid transported in xylem cells or phloem sieve tube elements of a plant. These cells transport water and nutrients throughout the plant.

<span class="mw-page-title-main">Symplast</span> Interconnected intracellular space of a plant

The symplast of a plant is the region enclosed by the cell membranes, within which water and solutes can diffuse freely. By contrast the apoplast is any fluid-filled space within the cell wall and extracellular space. Neighbouring cells are interconnected by microscopic channels known as plasmodesmata that traverse the cell walls. These channels, allow the flow of small molecules such as sugars, amino acids, and ions between cells. Larger molecules, including transcription factors and plant viruses, can also be transported through with the help of actin structures. The symplast allows direct cytoplasm-to-cytoplasm flow of water and other nutrients along concentration gradients. In particular, symplastic flow is used in the root systems to bring in nutrients from soil. Nutrient solutes move in this way through three skin layers of the roots: from cells of the epidermis, the outermost layer, through the cortex into the endodermis.

<span class="mw-page-title-main">Plasmodesma</span> A pore connecting between adjacent plant cells

Plasmodesmata are microscopic channels which traverse the cell walls of plant cells and some algal cells, enabling transport and communication between them. Plasmodesmata evolved independently in several lineages, and species that have these structures include members of the Charophyceae, Charales, Coleochaetales and Phaeophyceae, as well as all embryophytes, better known as land plants. Unlike animal cells, almost every plant cell is surrounded by a polysaccharide cell wall. Neighbouring plant cells are therefore separated by a pair of cell walls and the intervening middle lamella, forming an extracellular domain known as the apoplast. Although cell walls are permeable to small soluble proteins and other solutes, plasmodesmata enable direct, regulated, symplastic transport of substances between cells. There are two forms of plasmodesmata: primary plasmodesmata, which are formed during cell division, and secondary plasmodesmata, which can form between mature cells.

<span class="mw-page-title-main">Ground tissue</span> 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. This tissue system is present between the dermal tissue and forms the main bulk of the plant body.

  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.
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Pentaphragma is a genus of flowering plants. Pentaphragma is the sole genus in Pentaphragmataceae, a family in the order Asterales. These species are fleshy herbs, with asymmetrical leaf blades. They are found in Southeast Asia. Pentaphragma is rayless, but eventually develops rays in at least one of the species studied. This is interpreted as related to secondary woodiness or upright habit within a predominantly herbaceous phylad. The vessel elements of Pentaphragma have features universally interpreted as primitive in dicotyledons: scalariform perforation plates with numerous bars; pit membrane remnants in perforations; scalariform lateral wall pitting; the genus also has fiber-tracheids with prominently bordered pits. The presence of occasional scalariform perforation plates, often aberrant, in secondary xylem of families of Asterales sensu lato - Campanulaceae, Pentaphragmataceae, Valerianaceae, and even Asteraceae - can be attributed to paedomorphosis, extending these plates into secondary xylem from primary xylem. Raylessness in Pentaphragma can be described in terms of secondary woodiness or paedomorphosis. The fact that fiber-tracheids are shorter than vessel elements in Pentaphragma is believed related to raylessness also, because some fiber-tracheids are produced from 'potential' ray areas.

<span class="mw-page-title-main">Vessel element</span> Component of Xylem

A vessel element or vessel member is one of the cell types found in xylem, the water conducting tissue of plants. Vessel elements are found in angiosperms but absent from gymnosperms such as conifers. Vessel elements are the main feature distinguishing the "hardwood" of angiosperms from the "softwood" of conifers.

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In chemical biology, tonicity is a measure of the effective osmotic pressure gradient; the water potential of two solutions separated by a partially-permeable cell membrane. Tonicity depends on the relative concentration of selective membrane-impermeable solutes across a cell membrane which determine the direction and extent of osmotic flux. It is commonly used when describing the swelling-versus-shrinking response of cells immersed in an external solution.

The pressure flow hypothesis, also known as the mass flow hypothesis, is the best-supported theory to explain the movement of sap through the phloem. It was proposed by Ernst Münch, a German plant physiologist in 1930. A high concentration of organic substances, particularly sugar, inside cells of the phloem at a source, such as a leaf, creates a diffusion gradient that draws water into the cells from the adjacent xylem. This creates turgor pressure, also known as hydrostatic pressure, in the phloem. Movement of phloem sap occurs by bulk flow from sugar sources to sugar sinks. The movement in phloem is bidirectional, whereas, in xylem cells, it is unidirectional (upward). Because of this multi-directional flow, coupled with the fact that sap cannot move with ease between adjacent sieve-tubes, it is not unusual for sap in adjacent sieve-tubes to be flowing in opposite directions.

<span class="mw-page-title-main">Transpiration</span> Process of water moving through a plant parts

Transpiration is the process of water movement through a plant and its evaporation from aerial parts, such as leaves, stems and flowers. Water is necessary for plants but only a small amount of water taken up by the roots is used for growth and metabolism. The remaining 97–99.5% is lost by transpiration and guttation. Leaf surfaces are dotted with pores called stomata, and in most plants they are more numerous on the undersides of the foliage. The stomata are bordered by guard cells and their stomatal accessory cells that open and close the pore. Transpiration occurs through the stomatal apertures, and can be thought of as a necessary "cost" associated with the opening of the stomata to allow the diffusion of carbon dioxide gas from the air for photosynthesis. Transpiration also cools plants, changes osmotic pressure of cells, and enables mass flow of mineral nutrients and water from roots to shoots. Two major factors influence the rate of water flow from the soil to the roots: the hydraulic conductivity of the soil and the magnitude of the pressure gradient through the soil. Both of these factors influence the rate of bulk flow of water moving from the roots to the stomatal pores in the leaves via the xylem.

Franhueberia is an extinct monospecific genus of vascular land plants described from Early Devonian outcrops of the Battery Point Formation along the south shore of Gaspé Bay, Quebec, Canada.

References

  1. Jeremy Burgess (1985). Introduction to Plant Cell Development. CUP Archive. p. 91. ISBN   9780521316118.
  2. Ray F. Evert (2006). Esau's Plant Anatomy: Meristems, Cells, and Tissues of the Plant Body: Their Structure, Function, and Development (third, illustrated ed.). John Wiley & Sons. p. 76. ISBN   9780470047378.
  3. 1 2 3 Katherine Easu (1977). Anatomy of Seed Plants. Plant Anatomy (2nd ed.). John Wiley & Sons. p. 51. ISBN   0-471-24520-8.
  4. B. A. Meylan, Brian Geoffrey Butterfield (1972). Three-dimensional Structure of Wood: A Scanning Electron Microscope Study; Volume 2 of Syracuse wood science series (illustrated ed.). Syracuse University Press. p. 12. ISBN   9780815650300.
  5. "Pits in Plants | EasyBiologyClass". www.easybiologyclass.com. 2016-03-12. Retrieved 2023-08-31.
  6. Charles B. Beck (2010). An Introduction to Plant Structure and Development: Plant Anatomy for the Twenty-First Century (second, revised ed.). Cambridge University Press. p. 31. ISBN   9781139486361.
  7. Petty JA (1972). "The Aspiration of Bordered Pits in Conifer Wood". Proceedings of the Royal Society of London. Series B, Biological Sciences. 181 (1065): 395–406.

Further reading