The Fagales are an order of flowering plants, including some of the best-known trees. The order name is derived from beeches, they belong among the rosid group of dicotyledons. The families and genera included are as follows: Betulaceae - birch family Casuarinaceae - she-oak family Fagaceae - beech family Juglandaceae - walnut family Myricaceae - bayberry family Nothofagaceae - southern beech family Ticodendraceae - ticodendron family The older Cronquist system only included four families; the other families were split into three different orders, placed among the Hamamelidae. The Casuarinales comprised the single family Casuarinaceae, the Juglandales comprised the Juglandaceae and Rhoipteleaceae, the Myricales comprised the remaining forms; the change is due to studies suggesting the Myricales, so defined, are paraphyletic to the other two groups. Modern molecular phylogenetics suggest the following relationships: Missouri Botanical Gardens - Fagales
Plants are multicellular, predominantly photosynthetic eukaryotes of the kingdom Plantae. Plants were treated as one of two kingdoms including all living things that were not animals, all algae and fungi were treated as plants. However, all current definitions of Plantae exclude the fungi and some algae, as well as the prokaryotes. By one definition, plants form the clade Viridiplantae, a group that includes the flowering plants and other gymnosperms and their allies, liverworts and the green algae, but excludes the red and brown algae. Green plants obtain most of their energy from sunlight via photosynthesis by primary chloroplasts that are derived from endosymbiosis with cyanobacteria, their chloroplasts contain b, which gives them their green color. Some plants are parasitic or mycotrophic and have lost the ability to produce normal amounts of chlorophyll or to photosynthesize. Plants are characterized by sexual reproduction and alternation of generations, although asexual reproduction is common.
There are about 320 thousand species of plants, of which the great majority, some 260–290 thousand, are seed plants. Green plants provide a substantial proportion of the world's molecular oxygen and are the basis of most of Earth's ecosystems on land. Plants that produce grain and vegetables form humankind's basic foods, have been domesticated for millennia. Plants have many cultural and other uses, as ornaments, building materials, writing material and, in great variety, they have been the source of medicines and psychoactive drugs; the scientific study of plants is known as a branch of biology. All living things were traditionally placed into one of two groups and animals; this classification may date from Aristotle, who made the distincton between plants, which do not move, animals, which are mobile to catch their food. Much when Linnaeus created the basis of the modern system of scientific classification, these two groups became the kingdoms Vegetabilia and Animalia. Since it has become clear that the plant kingdom as defined included several unrelated groups, the fungi and several groups of algae were removed to new kingdoms.
However, these organisms are still considered plants in popular contexts. The term "plant" implies the possession of the following traits multicellularity, possession of cell walls containing cellulose and the ability to carry out photosynthesis with primary chloroplasts; when the name Plantae or plant is applied to a specific group of organisms or taxon, it refers to one of four concepts. From least to most inclusive, these four groupings are: Another way of looking at the relationships between the different groups that have been called "plants" is through a cladogram, which shows their evolutionary relationships; these are not yet settled, but one accepted relationship between the three groups described above is shown below. Those which have been called "plants" are in bold; the way in which the groups of green algae are combined and named varies between authors. Algae comprise several different groups of organisms which produce food by photosynthesis and thus have traditionally been included in the plant kingdom.
The seaweeds range from large multicellular algae to single-celled organisms and are classified into three groups, the green algae, red algae and brown algae. There is good evidence that the brown algae evolved independently from the others, from non-photosynthetic ancestors that formed endosymbiotic relationships with red algae rather than from cyanobacteria, they are no longer classified as plants as defined here; the Viridiplantae, the green plants – green algae and land plants – form a clade, a group consisting of all the descendants of a common ancestor. With a few exceptions, the green plants have the following features in common, they undergo closed mitosis without centrioles, have mitochondria with flat cristae. The chloroplasts of green plants are surrounded by two membranes, suggesting they originated directly from endosymbiotic cyanobacteria. Two additional groups, the Rhodophyta and Glaucophyta have primary chloroplasts that appear to be derived directly from endosymbiotic cyanobacteria, although they differ from Viridiplantae in the pigments which are used in photosynthesis and so are different in colour.
These groups differ from green plants in that the storage polysaccharide is floridean starch and is stored in the cytoplasm rather than in the plastids. They appear to have had a common origin with Viridiplantae and the three groups form the clade Archaeplastida, whose name implies that their chloroplasts were derived from a single ancient endosymbiotic event; this is the broadest modern definition of the term'plant'. In contrast, most other algae not only have different pigments but have chloroplasts with three or four surrounding membranes, they are not close relatives of the Archaeplastida having acquired chloroplasts separately from ingested or symbiotic green and red algae. They are thus not included in the broadest modern definition of the plant kingdom, although they were in the past; the green plants or Viridiplantae were traditionally divided into the green algae (including
Allocasuarina is a genus of trees in the flowering plant family Casuarinaceae. They are endemic to Australia, occurring in the south. Like the related genus Casuarina, they are called sheoaks or she-oaks. Wilson and Johnson distinguish the two closely related genera and Allocasuarina on the basis of: Casuarina: the mature samaras being grey or yellow-brown, dull, they are trees or shrubs that are notable for their long, segmented branchlets that function as leaves. Formally termed cladodes, these branchlets somewhat resemble pine needles, although sheoaks are flowering plants; the leaves are reduced to minute scales encircling each joint. Fallen cladodes form a dense, soft mat beneath sheoaks, preventing the development of undergrowth and making sheoak woods remarkably quiet. Another characteristic feature are the spiny "cones", about the size of an acorn but with a texture more resembling a conifer cone. However, sheoak "cones" are a woody fruit. Male specimens bear no fruit and are sometimes colloquially referred to as a "heoak".
As with legumes, sheoak roots possess nodules containing symbiotic nitrogen fixing bacteria. However, sheoaks are much less bushfire-tolerant than eucalypts. Fossils of related species have been found dating back to the time of Gondwana; the hard wood and rich texture makes sheoak wood popular among wood-turners. Sheoak wood is regarded as an excellent firewood as it burns with little ash; because of its ability to grow and develop extensive root systems in poor or sandy soils, to cover the ground with its "needles", it is used to stabilise soils in erosion prone areas, or on sand dunes. Sheoak is used as an ornamental shrub, although for this purpose the mat of "needles" may become a nuisance and must be considered. She-Oak Woodland & Forest Research team from IRD working on Casuarinaceae
A shrub or bush is a small- to medium-sized woody plant. Unlike herbaceous plants, shrubs have persistent woody, they are distinguished from trees by their multiple stems and shorter height, are under 6 m tall. Plants of many species may grow either depending on their growing conditions. Small, low shrubs less than 2 m tall, such as lavender and most small garden varieties of rose, are termed "subshrubs". An area of cultivated shrubs in a park or a garden is known as a shrubbery; when clipped as topiary, suitable species or varieties of shrubs develop dense foliage and many small leafy branches growing close together. Many shrubs respond well to renewal pruning, in which hard cutting back to a "stool" results in long new stems known as "canes". Other shrubs respond better to selective pruning to reveal their character. Shrubs in common garden practice are considered broad-leaved plants, though some smaller conifers such as mountain pine and common juniper are shrubby in structure. Species that grow into a shrubby habit may be either evergreen.
In botany and ecology, a shrub is more used to describe the particular physical structural or plant life-form of woody plants which are less than 8 metres high and have many stems arising at or near the base. For example, a descriptive system adopted in Australia is based on structural characteristics based on life-form, plus the height and amount of foliage cover of the tallest layer or dominant species. For shrubs 2–8 metres high the following structural forms are categorized: dense foliage cover — closed-shrub mid-dense foliage cover — open-shrub sparse foliage cover — tall shrubland sparse foliage cover — tall open shrublandFor shrubs less than 2 metres high the following structural forms are categorized: dense foliage cover — closed-heath or closed low shrubland— mid-dense foliage cover — open-heath or mid-dense low shrubland— sparse foliage cover — low shrubland sparse foliage cover — low open shrubland Those marked with * can develop into tree form
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
A stem is one of two main structural axes of a vascular plant, the other being the root. The stem is divided into nodes and internodes: The nodes hold one or more leaves, as well as buds which can grow into branches. Adventitious roots may be produced from the nodes; the internodes distance one node from another. The term "shoots" is confused with "stems". In most plants stems are located above the soil surface but some plants have underground stems. Stems have four main functions which are: Support for and the elevation of leaves and fruits; the stems keep the leaves in the light and provide a place for the plant to keep its flowers and fruits. Transport of fluids between the roots and the shoots in the xylem and phloem Storage of nutrients Production of new living tissue; the normal lifespan of plant cells is one to three years. Stems have cells called meristems. Stems are specialized for storage, asexual reproduction, protection or photosynthesis, including the following: Acaulescent – used to describe stems in plants that appear to be stemless.
These stems are just short, the leaves appearing to rise directly out of the ground, e.g. some Viola species. Arborescent – tree like with woody stems with a single trunk. Axillary bud – a bud which grows at the point of attachment of an older leaf with the stem, it gives rise to a shoot. Branched – aerial stems are described as being branched or unbranched Bud – an embryonic shoot with immature stem tip. Bulb – a short vertical underground stem with fleshy storage leaves attached, e.g. onion, tulip. Bulbs function in reproduction by splitting to form new bulbs or producing small new bulbs termed bulblets. Bulbs are a combination of stem and leaves so may better be considered as leaves because the leaves make up the greater part. Caespitose – when stems grow in a tangled mass or clump or in low growing mats. Cladode – a flattened stem that appears more-or-less leaf like and is specialized for photosynthesis, e.g. cactus pads. Climbing -- stems that wrap around other plants or structures. Corm – a short enlarged underground, storage stem, e.g. taro, gladiolus.
Decumbent -- stems that lie flat on the turn upwards at the ends. Fruticose -- stems. Herbaceous – non woody, they die at the end of the growing season. Internode – an interval between two successive nodes, it possesses the ability to elongate, either from its base or from its extremity depending on the species. Node – a point of attachment of a leaf or a twig on the stem in seed plants. A node is a small growth zone. Pedicel – stems that serve as the stalk of an individual flower in an inflorescence or infrutescence. Peduncle – a stem that supports an inflorescence Prickle – a sharpened extension of the stem's outer layers, e.g. roses. Pseudostem – a false stem made of the rolled bases of leaves, which may be 2 or 3 m tall as in banana Rhizome – a horizontal underground stem that functions in reproduction but in storage, e.g. most ferns, iris Runner – a type of stolon, horizontally growing on top of the ground and rooting at the nodes, aids in reproduction. E.g. garden strawberry, Chlorophytum comosum.
Scape – a stem that holds flowers that comes out of the ground and has no normal leaves. Hosta, Iris, Garlic. Stolon – a horizontal stem that produces rooted plantlets at its nodes and ends, forming near the surface of the ground. Thorn – a modified stem with a sharpened point. Tuber – a swollen, underground storage stem adapted for storage and reproduction, e.g. potato. Woody – hard textured stems with secondary xylem. Stem consist of three tissues, dermal tissue, ground tissue and vascular tissue; the dermal tissue covers the outer surface of the stem and functions to waterproof and control gas exchange. The ground tissue consists of parenchyma cells and fills in around the vascular tissue, it sometimes functions in photosynthesis. Vascular tissue provides structural support. Most or all ground tissue may be lost in woody stems; the dermal tissue of aquatic plants stems. The arrangement of the vascular tissues varies among plant species. Dicot stems with primary growth have pith in the center, with vascular bundles forming a distinct ring visible when the stem is viewed in cross section.
The outside of the stem is covered with an epidermis, covered by a waterproof cuticle. The epidermis may contain stomata for gas exchange and multicellular stem hairs called trichomes. A cortex consisting of hypodermis and endodermis is present above the pericycle and vascular bundles. Woody dicots and many nonwoody dicots have secondary growth originating from their lateral or secondary meristems: the vascular cambium and the cork cambium or phellogen; the vascular cambium forms between the xylem and phloem in the vascular bundles and connects to form a continuous cylinder. The vascular cambium cells divide to produce secondary xylem to the inside and secondary phloem to the outside; as the stem increases in diameter due to production of secondary xylem and secondary phloem, the cortex and epidermis are destroyed. Before the cortex is destroyed, a cork cambium develops there; the cork cambium divides to produce waterproof cork cells externally and sometimes phelloderm cells internally. Those three tissues form the periderm.
Areas of loosely pack
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