Organs are groups of tissues with similar functions. Plant and animal life relies on many organs. Organs are composed of main tissue, "sporadic" tissues, stroma; the main tissue is that, unique for the specific organ, such as the myocardium, the main tissue of the heart, while sporadic tissues include the nerves, blood vessels, connective tissues. The main tissues that make up an organ tend to have common embryologic origins, such as arising from the same germ layer. Functionally-related organs cooperate to form whole organ systems. Organs exist in most multicellular organisms. In single-celled organisms such as bacteria, the functional analogue of an organ is known as an organelle. In plants there are three main organs. A hollow organ is an internal organ that forms a hollow tube, or pouch such as the stomach, intestine, or bladder. In the study of anatomy, the term viscus is used to refer to an internal organ, viscera is the plural form. 79 organs have been identified in the human body. In biology, tissue is a cellular organizational level between complete organs.
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 formed by the functional grouping together of multiple tissues; the study of human and animal tissues is known as histology or, in connection with disease, histopathology. For plants, the discipline is called plant morphology. Classical tools for studying tissues include the paraffin block in which tissue is embedded and sectioned, the histological stain, the optical microscope. In the last couple of decades, developments in electron microscopy, immunofluorescence, the use of frozen tissue sections have enhanced the detail that can be observed in tissues. With these tools, the classical appearances of tissues can be examined in health and disease, enabling considerable refinement of medical diagnosis and prognosis. Two or more organs working together in the execution of a specific body function form an organ system called a biological system or body system.
The functions of organ systems share significant overlap. For instance, the nervous and endocrine system both operate via the hypothalamus. For this reason, the two systems are studied as the neuroendocrine system; the same is true for the musculoskeletal system because of the relationship between the muscular and skeletal systems. Common organ system designations in plants includes the differentiation of root. All parts of the plant above ground, including the functionally distinct leaf and flower organs, may be classified together as the shoot organ system. Animals such as humans have a variety of organ systems; these specific systems are widely studied in human anatomy. Cardiovascular system: pumping and channeling blood to and from the body and lungs with heart and blood vessels. Digestive system: digestion and processing food with salivary glands, stomach, gallbladder, intestines, colon and anus. Endocrine system: communication within the body using hormones made by endocrine glands such as the hypothalamus, pituitary gland, pineal body or pineal gland, thyroid and adrenals, i.e. adrenal glands.
Excretory system: kidneys, ureters and urethra involved in fluid balance, electrolyte balance and excretion of urine. Lymphatic system: structures involved in the transfer of lymph between tissues and the blood stream, the lymph and the nodes and vessels that transport it including the Immune system: defending against disease-causing agents with leukocytes, adenoids and spleen. Integumentary system: skin and nails of mammals. Scales of fish and birds, feathers of birds. Muscular system: movement with muscles. Nervous system: collecting and processing information with brain, spinal cord and nerves. Reproductive system: the sex organs, such as ovaries, fallopian tubes, vulva, testes, vas deferens, seminal vesicles and penis. Respiratory system: the organs used for breathing, the pharynx, trachea, bronchi and diaphragm. Skeletal system: structural support and protection with bones, cartilage and tendons; the study of plant organs is referred to as plant morphology, rather than anatomy – as in animal systems.
Organs of plants can be divided into reproductive. Vegetative plant organs include roots and leaves; the reproductive organs are variable. In flowering plants, they are represented by the flower and fruit. In conifers, the organ that bears the reproductive structures is called a cone. In other divisions of plants, the reproductive organs are called strobili, in Lycopodiophyta, or gametophores in mosses; the vegetative organs are essential for maintaining the life of a plant. While there can be 11 organ systems in animals, there are far fewer in plants, where some perform the vital functions, such as photosynthesis, while the reproductive organs are essential in reproduction. However, if there is asexual vegetative reproduction, the vegetative organs are those that create the new generation of plants. Many societies have a system for organ donation, in which a living or deceased donor's organ is transplanted into a person with a failing organ; the transplantation of larger solid organs requires immunosuppression to prevent organ rejection or graft-versus-host disease.
There is considerable interest throughout the world in creating laboratory-grown or artificial organs. The English word "organ" dates back in reference to any musical instrument. By the late 14th
Biomimetics or biomimicry is the imitation of the models and elements of nature for the purpose of solving complex human problems. The terms "biomimetics" and "biomimicry" derive from Ancient Greek: βίος, μίμησις, from μιμεῖσθαι, to imitate, from μῖμος, actor. A related field is bionics. Living organisms have evolved well-adapted structures and materials over geological time through natural selection. Biomimetics has given rise to new technologies inspired by biological solutions at macro and nanoscales. Humans have looked at nature for answers to problems throughout our existence. Nature has solved engineering problems such as self-healing abilities, environmental exposure tolerance and resistance, self-assembly, harnessing solar energy. One of the early examples of would-be biomimicry was the study of birds to enable human flight. Although never successful in creating a "flying machine", Leonardo da Vinci was a keen observer of the anatomy and flight of birds, made numerous notes and sketches on his observations as well as sketches of "flying machines".
The Wright Brothers, who succeeded in flying the first heavier-than-air aircraft in 1903 derived inspiration from observations of pigeons in flight. During the 1950s the American biophysicist and polymath Otto Schmitt developed the concept of "biomimetics". During his doctoral research he developed the Schmitt trigger by studying the nerves in squid, attempting to engineer a device that replicated the biological system of nerve propagation, he continued to focus on devices that mimic natural systems and by 1957 he had perceived a converse to the standard view of biophysics at that time, a view he would come to call biomimetics. Biophysics is not so much, it is an approach to problems of biological science utilizing the theory and technology of the physical sciences. Conversely, biophysics is a biologist's approach to problems of physical science and engineering, although this aspect has been neglected. In 1960 Jack E. Steele coined a similar term, bionics, at Wright-Patterson Air Force Base in Dayton, where Otto Schmitt worked.
Steele defined bionics as "the science of systems which have some function copied from nature, or which represent characteristics of natural systems or their analogues". During a meeting in 1963 Schmitt stated, Let us consider what bionics has come to mean operationally and what it or some word like it ought to mean in order to make good use of the technical skills of scientists specializing, or rather, I should say, despecializing into this area of research In 1969 Schmitt used the term “biomimetic“ in the title one of his papers, by 1974 it had found its way into Webster's Dictionary, bionics entered the same dictionary earlier in 1960 as "a science concerned with the application of data about the functioning of biological systems to the solution of engineering problems". Bionic took on a different connotation when Martin Caidin referenced Jack Steele and his work in the novel Cyborg which resulted in the 1974 television series The Six Million Dollar Man and its spin-offs; the term bionic became associated with "the use of electronically operated artificial body parts" and "having ordinary human powers increased by or as if by the aid of such devices".
Because the term bionic took on the implication of supernatural strength, the scientific community in English speaking countries abandoned it. The term biomimicry appeared as early as 1982. Biomimicry was popularized by scientist and author Janine Benyus in her 1997 book Biomimicry: Innovation Inspired by Nature. Biomimicry is defined in the book as a "new science that studies nature's models and imitates or takes inspiration from these designs and processes to solve human problems". Benyus suggests looking to Nature as a "Model and Mentor" and emphasizes sustainability as an objective of biomimicry. Biomimetics could in principle be applied in many fields; because of the diversity and complexity of biological systems, the number of features that might be imitated is large. Biomimetic applications are at various stages of development from technologies that might become commercially usable to prototypes. Murray's law, which in conventional form determined the optimum diameter of blood vessels, has been re-derived to provide simple equations for the pipe or tube diameter which gives a minimum mass engineering system.
Aircraft wing design and flight techniques are being inspired by bats. Biorobots based on the physiology and methods of locomotion of animals include BionicKangaroo which moves like a kangaroo, saving energy from one jump and transferring it to its next jump. Kamigami Robots, a children's toy, mimic cockroach locomotion to run and efficiently over indoor and outdoor surfaces. Researchers studied the termite's ability to maintain constant temperature and humidity in their termite mounds in Africa despite outside temperatures that vary from 1.5 °C to 40 °C. Researchers scanned a termite mound and created 3-D images of the mound structure, which revealed construction that could influence human building design; the Eastgate Centre, a mid-rise office complex in Harare, stays cool without air conditioning and uses only 10% of the energy of a conventional building of the same size. In structural engineering, the Swiss Federal Institute of Technology has incorporated biomimetic characteristics in an adaptive deployable "tensegrity" bridge.
The bridge can carry out self-diagnosis and self-repair. The arrangement of leaves on a plant has been adapted for better solar power collection. Analysis of the elastic deformation happening when a poll
The eudicots, Eudicotidae or eudicotyledons are a clade of flowering plants, called tricolpates or non-magnoliid dicots by previous authors. The botanical terms were introduced in 1991 by evolutionary botanist James A. Doyle and paleobotanist Carol L. Hotton to emphasize the evolutionary divergence of tricolpate dicots from earlier, less specialized, dicots; the close relationships among flowering plants with tricolpate pollen grains was seen in morphological studies of shared derived characters. These plants have a distinct trait in their pollen grains of exhibiting three colpi or grooves paralleling the polar axis. Molecular evidence confirmed the genetic basis for the evolutionary relationships among flowering plants with tricolpate pollen grains and dicotyledonous traits; the term means "true dicotyledons", as it contains the majority of plants that have been considered dicots and have characteristics of the dicots. The term "eudicots" has subsequently been adopted in botany to refer to one of the two largest clades of angiosperms, monocots being the other.
The remaining angiosperms include magnoliids and what are sometimes referred to as basal angiosperms or paleodicots, but these terms have not been or adopted, as they do not refer to a monophyletic group. The other name for the eudicots is tricolpates, a name which refers to the grooved structure of the pollen. Members of the group have tricolpate pollen; these pollens have three or more pores set in furrows called colpi. In contrast, most of the other seed plants produce monosulcate pollen, with a single pore set in a differently oriented groove called the sulcus; the name "tricolpates" is preferred by some botanists to avoid confusion with the dicots, a nonmonophyletic group. Numerous familiar plants are eudicots, including many common food plants and ornamentals; some common and familiar eudicots include members of the sunflower family such as the common dandelion, the forget-me-not and other members of its family, buttercup and macadamia. Most leafy trees of midlatitudes belong to eudicots, with notable exceptions being magnolias and tulip trees which belong to magnoliids, Ginkgo biloba, not an angiosperm.
The name "eudicots" is used in the APG system, of 1998, APG II system, of 2003, for classification of angiosperms. It is applied to a monophyletic group, which includes most of the dicots. "Tricolpate" is a synonym for the "Eudicot" monophyletic group, the "true dicotyledons". The number of pollen grain furrows or pores helps classify the flowering plants, with eudicots having three colpi, other groups having one sulcus. Pollen apertures are any modification of the wall of the pollen grain; these modifications include thinning and pores, they serve as an exit for the pollen contents and allow shrinking and swelling of the grain caused by changes in moisture content. The elongated apertures/ furrows in the pollen grain are called colpi, along with pores, are a chief criterion for identifying the pollen classes; the eudicots can be divided into two groups: the basal eudicots and the core eudicots. Basal eudicot is an informal name for a paraphyletic group; the core eudicots are a monophyletic group.
A 2010 study suggested the core eudicots can be divided into two clades, Gunnerales and a clade called "Pentapetalae", comprising all the remaining core eudicots. The Pentapetalae can be divided into three clades: Dilleniales superrosids consisting of Saxifragales and rosids superasterids consisting of Santalales, Berberidopsidales and asteridsThis division of the eudicots is shown in the following cladogram: The following is a more detailed breakdown according to APG IV, showing within each clade and orders: clade Eudicots order Ranunculales order Proteales order Trochodendrales order Buxales clade Core eudicots order Gunnerales order Dilleniales clade Superrosids order Saxifragales clade Rosids order Vitales clade Fabids order Fabales order Rosales order Fagales order Cucurbitales order Oxalidales order Malpighiales order Celastrales order Zygophyllales clade Malvids order Geraniales order Myrtales order Crossosomatales order Picramniales order Malvales order Brassicales order Huerteales order Sapindales clade Superasterids order Berberidopsidales order Santalales order Caryophyllales clade Asterids order Cornales order Ericales clade Campanulids order Aquifoliales order Asterales order Escalloniales order Bruniales order Apiales order Dipsacales order Paracryphiales clade Lamiids order Solanales order Lamiales order Vahliales order Gentianales order Boraginales order Garryales order Metteniusales order Icacinales Eudicots at the Encyclopedia of Life Eudicots, Tree of Life Web Project Dicots Plant Life Forms
Plant pathology is the scientific study of diseases in plants caused by pathogens and environmental conditions. Organisms that cause infectious disease include fungi, bacteria, viroids, virus-like organisms, protozoa and parasitic plants. Not included are ectoparasites like insects, vertebrate, or other pests that affect plant health by eating of plant tissues. Plant pathology involves the study of pathogen identification, disease etiology, disease cycles, economic impact, plant disease epidemiology, plant disease resistance, how plant diseases affect humans and animals, pathosystem genetics, management of plant diseases. Control of plant diseases is crucial to the reliable production of food, it provides significant problems in agricultural use of land, water and other inputs. Plants in both natural and cultivated populations carry inherent disease resistance, but there are numerous examples of devastating plant disease impacts such as Irish potato famine and chestnut blight, as well as recurrent severe plant diseases like rice blast, soybean cyst nematode, citrus canker.
However, disease control is reasonably successful for most crops. Disease control is achieved by use of plants that have been bred for good resistance to many diseases, by plant cultivation approaches such as crop rotation, use of pathogen-free seed, appropriate planting date and plant density, control of field moisture, pesticide use. Across large regions and many crop species, it is estimated that diseases reduce plant yields by 10% every year in more developed settings, but yield loss to diseases exceeds 20% in less developed settings. Continuing advances in the science of plant pathology are needed to improve disease control, to keep up with changes in disease pressure caused by the ongoing evolution and movement of plant pathogens and by changes in agricultural practices. Plant diseases cause major economic losses for farmers worldwide; the Food and Agriculture Organization estimates indeed that pests and diseases are responsible for about 25% of crop loss. To solve this issue, new methods are needed to detect diseases and pests early, such as novel sensors that detect plant odours and spectroscopy and biophotonics that are able to diagnose plant health and metabolism.
Most phytopathogenic fungi belong to the Ascomycetes and the Basidiomycetes. The fungi reproduce both sexually and asexually via the production of other structures. Spores may be spread long distances by air or water. Many soil inhabiting fungi are capable of living saprotrophically, carrying out the part of their life cycle in the soil; these are facultative saprotrophs. Fungal diseases may be controlled through the use of other agriculture practices. However, new races of fungi evolve that are resistant to various fungicides. Biotrophic fungal pathogens colonize living plant tissue and obtain nutrients from living host cells. Necrotrophic fungal pathogens infect and kill host tissue and extract nutrients from the dead host cells. Significant fungal plant pathogens include: Fusarium spp. Thielaviopsis spp. Verticillium spp. Magnaporthe grisea Sclerotinia sclerotiorum Ustilago spp. smut of barley Rhizoctonia spp. Phakospora pachyrhizi Puccinia spp. Armillaria spp; the oomycetes are fungus-like organisms.
They include some of the most destructive plant pathogens including the genus Phytophthora, which includes the causal agents of potato late blight and sudden oak death. Particular species of oomycetes are responsible for root rot. Despite not being related to the fungi, the oomycetes have developed similar infection strategies. Oomycetes are capable of using effector proteins to turn off a plant's defenses in its infection process. Plant pathologists group them with fungal pathogens. Significant oomycete plant pathogens include: Pythium spp. Phytophthora spp. including the potato blight of the Great Irish Famine Some slime molds in Phytomyxea cause important diseases, including club root in cabbage and its relatives and powdery scab in potatoes. These are caused by species of Spongospora, respectively. Most bacteria that are associated with plants are saprotrophic and do no harm to the plant itself. However, a small number, around 100 known species, are able to cause disease. Bacterial diseases are much more prevalent in tropical regions of the world.
Most plant pathogenic bacteria are rod-shaped. In order to be able to colonize the plant they have specific pathogenicity factors. Five main types of bacterial pathogenicity factors are known: uses of cell wall–degrading enzymes, effector proteins and exopolysaccharides. Pathogens such as Erwinia species use cell wall–degrading enzymes to cause soft rot. Agrobacterium species change the level of auxins to cause tumours with phytohormones. Exopolysaccharides are produced by bacteria and block xylem vessels leading to the death of the plant. Bacteria control the production of pathogenicity factors via quorum sensing. Significant bacterial plant pathogens: Burkholderia Proteobacteria Xanthomonas spp. Pseudomonas spp. Pseudomonas syringae pv. tomato causes tomato plants to produce less fruit, it "continues to adapt to the tomato by minimizing its recognition by the tomato immune system." Phytoplasma and Spiroplasma are genera of bacteria that lack cell walls and are related to the mycoplasmas, which are human pathogens.
Together they are referred to
Bark is the outermost layers of stems and roots of woody plants. Plants with bark include trees, woody vines, shrubs. Bark is a nontechnical term, it consists of the inner bark and the outer bark. The inner bark, which in older stems is living tissue, includes the innermost area of the periderm; the outer bark in older stems includes the dead tissue on the surface of the stems, along with parts of the innermost periderm and all the tissues on the outer side of the periderm. The outer bark on trees which lies external to the last formed periderm is called the rhytidome. Products derived from bark include: bark shingle siding and wall coverings and other flavorings, tanbark for tannin, latex, poisons, various hallucinogenic chemicals and cork. Bark has been used to make cloth and ropes and used as a surface for paintings and map making. A number of plants are grown for their attractive or interesting bark colorations and surface textures or their bark is used as landscape mulch. What is called bark includes a number of different tissues.
Cork is an external, secondary tissue, impermeable to water and gases, is called the phellem. The cork is produced by the cork cambium, a layer of meristematically active cells which serve as a lateral meristem for the periderm; the cork cambium, called the phellogen, is only one cell layer thick and it divides periclinally to the outside producing cork. The phelloderm, not always present in all barks, is a layer of cells formed by and interior to the cork cambium. Together, the phellem and phelloderm constitute the periderm. Cork cell walls contain suberin, a waxy substance which protects the stem against water loss, the invasion of insects into the stem, prevents infections by bacteria and fungal spores; the cambium tissues, i.e. the cork cambium and the vascular cambium, are the only parts of a woody stem where cell division occurs. Phloem is a nutrient-conducting tissue composed of sieve tubes or sieve cells mixed with parenchyma and fibers; the cortex is the primary tissue of roots. In stems the cortex is between the epidermis layer and the phloem, in roots the inner layer is not phloem but the pericycle.
From the outside to the inside of a mature woody stem, the layers include: Bark Periderm Cork, includes the rhytidome Cork cambium Phelloderm Cortex Phloem Vascular cambium Wood Sapwood Heartwood Pith In young stems, which lack what is called bark, the tissues are, from the outside to the inside: Epidermis, which may be replaced by periderm Cortex Primary and secondary phloem Vascular cambium Secondary and primary xylem. As the stem ages and grows, changes occur that transform the surface of the stem into the bark; the epidermis is a layer of cells that cover the plant body, including the stems, leaves and fruits, that protects the plant from the outside world. In old stems the epidermal layer and primary phloem become separated from the inner tissues by thicker formations of cork. Due to the thickening cork layer these cells die; this dead layer is the rough corky bark that forms around other stems. A secondary covering called the periderm forms on small woody stems and many non-woody plants, composed of cork, the cork cambium, the phelloderm.
The periderm forms from the phellogen. The periderm replaces the epidermis, acts as a protective covering like the epidermis. Mature phellem cells have suberin in their walls to protect the stem from desiccation and pathogen attack. Older phellem cells are dead; the skin on the potato tuber constitutes the cork of the periderm. In woody plants the epidermis of newly grown stems is replaced by the periderm in the year; as the stems grow a layer of cells form under the epidermis, called the cork cambium, these cells produce cork cells that turn into cork. A limited number of cell layers may form interior to the cork cambium, called the phelloderm; as the stem grows, the cork cambium produces new layers of cork which are impermeable to gases and water and the cells outside the periderm, namely the epidermis and older secondary phloem die. Within the periderm are lenticels, which form during the production of the first periderm layer. Since there are living cells within the cambium layers that need to exchange gases during metabolism, these lenticels, because they have numerous intercellular spaces, allow gaseous exchange with the outside atmosphere.
As the bark develops, new lenticels are formed within the cracks of the cork layers. The rhytidome is the most familiar part of bark, being the outer layer that covers the trunks of trees, it is composed of dead cells and is produced by the formation of multiple layers of suberized periderm and phloem tissue. The rhytidome is well developed in older stems and roots of trees. In shrubs, older bark is exfoliated and thick rhytidome accumulates, it is thickest and most distinctive at the trunk or bole of the tree. Bark tissues make up by weight between 10–20% of woody vascular plants and consists of various biopolymers, lignin, suberin and polysaccharides. Up to 40% of the bark tissue is made of lignin which forms an important part of a plant providing stru
The epidermis is a single layer of cells that covers the leaves, flowers and stems of plants. It forms a boundary between the external environment; the epidermis serves several functions: it protects against water loss, regulates gas exchange, secretes metabolic compounds, absorbs water and mineral nutrients. The epidermis of most leaves shows dorsoventral anatomy: the upper and lower 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; the epidermis is the outermost cell layer of the primary plant body. In some older works the cells of the leaf epidermis have been regarded as specialised parenchyma cells, but the established modern preference has long been to classify the epidermis as dermal tissue, whereas parenchyma is classified as ground tissue; the epidermis is the main component of the dermal tissue system of leaves, stems, flowers and seeds.
Most plants have an epidermis, a single cell layer thick. Some plants like Ficus elastica and Peperomia, which have periclinal cellular division within the protoderm of the leaves, have an epidermis with multiple cell layers. Epidermal cells are linked to each other and provide mechanical strength and protection to the plant; the walls of the epidermal cells of the above ground parts of plants contain cutin, are covered with a cuticle. The cuticle reduces water loss to the atmosphere, it is sometimes covered with wax in smooth sheets, plates, tubes or filaments; the wax layers give some plants a bluish surface color. Surface wax protects the plant from intense sunlight and wind; the underside of many leaves have a thinner cuticle than the top side, leaves of plants from dry climates have thickened cuticles to conserve water by reducing transpiration. The epidermal tissue includes several differentiated cell types: epidermal cells, guard cells, subsidiary cells, epidermal hairs; the epidermal cells are the most numerous and least specialized.
These are more elongated in the leaves of monocots than in those of dicots. Trichomes or hairs grow out from the epidermis in many species. In root epidermis, epidermal hairs, termed root hairs are common and are specialized for absorption of water and mineral nutrients. In plants with secondary growth, the epidermis of roots and stems is replaced by a periderm through the action of a cork cambium; the leaf and stem epidermis is covered with pores called stomata, part of a stoma complex consisting of a pore surrounded on each side by chloroplast-containing guard cells, two to four subsidiary cells that lack chloroplasts. The stomata complex regulates the exchange of gases and water vapor between the outside air and the interior of the leaf; the stomata are more numerous over the abaxial epidermis of the leaf than the upper epidermis. An exception is floating leaves where all stomata are on the upper surface. Vertical leaves, such as those of many grasses have equal numbers of stomata on both surfaces.
The stoma is bounded by two guard cells. The guard cells differ from the epidermal cells in the following aspects: The guard cells are bean-shaped in surface view, while the epidermal cells are irregular in shape The guard cells contain chloroplasts, so they can manufacture food by photosynthesis Guard cells are the only epidermal cells that can make sugar. According to one theory, in sunlight the concentration of potassium ions increases in the guard cells. This, together with the sugars formed, lowers the water potential in the guard cells; as a result, water from other cells enter the guard cells by osmosis so they swell and become turgid. Because the guard cells have a thicker cellulose wall on one side of the cell, i.e. the side around the stomatal pore, the swollen guard cells become curved and pull the stomata open. At night, the sugar is used up and water leaves the guard cells, so they become flaccid and the stomatal pore closes. In this way, they reduce the amount of water vapour escaping from the leaf.
The plant epidermis consists of three main cell types: pavement cells, guard cells and their subsidiary cells that surround the stomata and trichomes, otherwise known as leaf hairs. The epidermis of petals form a variation of trichomes called conical cells. Trichomes develop at a distinct phase during leaf development, under the control of two major trichome specification genes: TTG and GL1; the process may be controlled by the plant hormones gibberellins, if not controlled, gibberellins have an effect on the development of the leaf hairs. GL1 causes endoreplication, the replication of DNA without subsequent cell division as well as cell expansion. GL1 turns on the expression of a second gene for trichome formation, GL2, which controls the final stages of trichome formation causing the cellular outgrowth. Arabidopsis thaliana uses the products of inhibitory genes to control the patterning of trichomes, such as TTG and TRY; the products of these genes will diffuse into the lateral cells, preventing them from forming trichomes and in the case of TRY promoting the formation of pavement cells.
Expression of the gene MIXTA, or its analogue in other species in the process of cel
The flowering plants known as angiosperms, Angiospermae or Magnoliophyta, are the most diverse group of land plants, with 64 orders, 416 families 13,164 known genera and c. 369,000 known species. Like gymnosperms, angiosperms are seed-producing plants. However, they are distinguished from gymnosperms by characteristics including flowers, endosperm within the seeds, the production of fruits that contain the seeds. Etymologically, angiosperm means a plant; the term comes from the Greek words sperma. The ancestors of flowering plants diverged from gymnosperms in the Triassic Period, 245 to 202 million years ago, the first flowering plants are known from 160 mya, they diversified extensively during the Early Cretaceous, became widespread by 120 mya, replaced conifers as the dominant trees from 100 to 60 mya. Angiosperms differ from other seed plants in several ways, described in the table below; these distinguishing characteristics taken together have made the angiosperms the most diverse and numerous land plants and the most commercially important group to humans.
Angiosperm stems are made up of seven layers. The amount and complexity of tissue-formation in flowering plants exceeds that of gymnosperms; the vascular bundles of the stem are arranged such that the phloem form concentric rings. In the dicotyledons, the bundles in the young stem are arranged in an open ring, separating a central pith from an outer cortex. In each bundle, separating the xylem and phloem, is a layer of meristem or active formative tissue known as cambium. By the formation of a layer of cambium between the bundles, a complete ring is formed, a regular periodical increase in thickness results from the development of xylem on the inside and phloem on the outside; the soft phloem becomes crushed, but the hard wood persists and forms the bulk of the stem and branches of the woody perennial. Owing to differences in the character of the elements produced at the beginning and end of the season, the wood is marked out in transverse section into concentric rings, one for each season of growth, called annual rings.
Among the monocotyledons, the bundles are more numerous in the young stem and are scattered through the ground tissue. They once formed the stem increases in diameter only in exceptional cases; the characteristic feature of angiosperms is the flower. Flowers show remarkable variation in form and elaboration, provide the most trustworthy external characteristics for establishing relationships among angiosperm species; the function of the flower is to ensure fertilization of the ovule and development of fruit containing seeds. The floral apparatus may arise terminally from the axil of a leaf; as in violets, a flower arises singly in the axil of an ordinary foliage-leaf. More the flower-bearing portion of the plant is distinguished from the foliage-bearing or vegetative portion, forms a more or less elaborate branch-system called an inflorescence. There are two kinds of reproductive cells produced by flowers. Microspores, which will divide to become pollen grains, are the "male" cells and are borne in the stamens.
The "female" cells called megaspores, which will divide to become the egg cell, are contained in the ovule and enclosed in the carpel. The flower may consist only of these parts, as in willow, where each flower comprises only a few stamens or two carpels. Other structures are present and serve to protect the sporophylls and to form an envelope attractive to pollinators; the individual members of these surrounding structures are known as petals. The outer series is green and leaf-like, functions to protect the rest of the flower the bud; the inner series is, in general, white or brightly colored, is more delicate in structure. It functions to attract bird pollinators. Attraction is effected by color and nectar, which may be secreted in some part of the flower; the characteristics that attract pollinators account for the popularity of flowers and flowering plants among humans. While the majority of flowers are perfect or hermaphrodite, flowering plants have developed numerous morphological and physiological mechanisms to reduce or prevent self-fertilization.
Heteromorphic flowers have short carpels and long stamens, or vice versa, so animal pollinators cannot transfer pollen to the pistil. Homomorphic flowers may employ a biochemical mechanism called self-incompatibility to discriminate between self and non-self pollen grains. In other species, the male and female parts are morphologically separated, developing on different flowers; the botanical term "Angiosperm", from the Ancient Greek αγγείον, angeíon and σπέρμα, was coined in the form Angiospermae by Paul Hermann in 1690, as the name of one of his primary divisions of the plant kingdom. This included flowering plants possessing seeds enclosed in capsules, distinguished from his Gymnospermae, or flowering plants with achenial or schizo-carpic fruits, the whole fruit or each of its pieces being here regarded as a seed and naked; the term and its antonym were maintained by Carl Linnaeus with the same sense, but with restricted application, in the names of the orders of his class Didynamia. Its use with any