The term cultivar most refers to an assemblage of plants selected for desirable characters that are maintained during propagation. More cultivar refers to the most basic classification category of cultivated plants in the International Code of Nomenclature for Cultivated Plants. Most cultivars arose in cultivation. Popular ornamental garden plants like roses, daffodils and azaleas are cultivars produced by careful breeding and selection for floral colour and form; the world's agricultural food crops are exclusively cultivars that have been selected for characters such as improved yield and resistance to disease, few wild plants are now used as food sources. Trees used in forestry are special selections grown for their enhanced quality and yield of timber. Cultivars form a major part of Liberty Hyde Bailey's broader group, the cultigen, defined as a plant whose origin or selection is due to intentional human activity. A cultivar is not the same as a botanical variety, a taxonomic rank below subspecies, there are differences in the rules for creating and using the names of botanical varieties and cultivars.
In recent times, the naming of cultivars has been complicated by the use of statutory patents for plants and recognition of plant breeders' rights. The International Union for the Protection of New Varieties of Plants offers legal protection of plant cultivars to persons or organisations that introduce new cultivars to commerce. UPOV requires that a cultivar be "distinct, uniform", "stable". To be "distinct", it must have characters that distinguish it from any other known cultivar. To be "uniform" and "stable", the cultivar must retain these characters in repeated propagation; the naming of cultivars is an important aspect of cultivated plant taxonomy, the correct naming of a cultivar is prescribed by the Rules and Recommendations of the International Code of Nomenclature for Cultivated Plants. A cultivar is given a cultivar name, which consists of the scientific Latin botanical name followed by a cultivar epithet; the cultivar epithet is in a vernacular language. For example, the full cultivar name of the King Edward potato is Solanum tuberosum'King Edward'.'King Edward' is the cultivar epithet, according to the Rules of the Cultivated Plant Code, is bounded by single quotation marks.
The word cultivar originated from the need to distinguish between wild plants and those with characteristics that arose in cultivation, presently denominated cultigens. This distinction dates to the Greek philosopher Theophrastus, the "Father of Botany", keenly aware of this difference. Botanical historian Alan Morton noted that Theophrastus in his Historia Plantarum "had an inkling of the limits of culturally induced changes and of the importance of genetic constitution"; the International Code of Nomenclature for algae and plants uses as its starting point for modern botanical nomenclature the Latin names in Linnaeus' Species Plantarum and Genera Plantarum. In Species Plantarum, Linnaeus enumerated all plants known to him, either directly or from his extensive reading, he recognised the rank of varietas and he indicated these varieties with letters of the Greek alphabet, such as α, β, λ, before the varietal name, rather than using the abbreviation "var." as is the present convention. Most of the varieties that Linnaeus enumerated were of "garden" origin rather than being wild plants.
In time the need to distinguish between wild plants and those with variations, cultivated increased. In the nineteenth century many "garden-derived" plants were given horticultural names, sometimes in Latin and sometimes in a vernacular language. From circa the 1900s, cultivated plants in Europe were recognised in the Scandinavian and Slavic literature as stamm or sorte, but these words could not be used internationally because, by international agreement, any new denominations had to be in Latin. In the twentieth century an improved international nomenclature was proposed for cultivated plants. Liberty Hyde Bailey of Cornell University in New York, United States created the word cultivar in 1923 when he wrote that: The cultigen is a species, or its equivalent, that has appeared under domestication – the plant is cultigenous. I now propose another name, for a botanical variety, or for a race subordinate to species, that has originated under cultivation, it is the equivalent of the botanical variety except in respect to its origin.
In that essay, Bailey used only the rank of species for the cultigen, but it was obvious to him that many domesticated plants were more like botanical varieties than species, that realization appears to have motivated the suggestion of the new category of cultivar. Bailey created the word cultivar, assumed to be a portmanteau of cultivated and variety. Bailey never explicitly stated the etymology of cultivar, it has been suggested that it is instead a contraction of cultigen and variety, which seems correct; the neologism cultivar was promoted as "euphonious" and "free from ambiguity". The first Cultivated Plant Code of 1953 subsequently commended its use, by 1960 it had achieved common international acceptance; the words cultigen and cultivar may be confused with
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
Laeliinae is a Neotropical subtribe including 40 orchid genera, such as Brassavola and Cattleya. The genus Epidendrum is the largest within this subtribe; this is followed with over 120 species. Genus and Number of Species: Acrorchis Dressler, 1 Adamantinia Van den Berg & M. W. Chase, 1 Alamania La Llave & Lex. 1 Arpophyllum La Llave & Lex, 5 Artorima Dressler & G. E. Pollard, 1 Barkeria Knowles & Westc. 17 Syn. Dothilophis Raf. Brassavola R. Br. 17 Broughtonia R. Br. 6 Syn. Cattleyopsis Lem. Laeliopsis Lindl. Cattleya Lindl. 118 Syn. Maelenia Dum. Sophronitis Lindl. Sophronia Lindl. Lophoglottis Raf. Hoffmannseggella H. G. Jones, Hadrolaelia Chiron & V. P. Castro, Dungsia Chiron & V. P. Castro, Microlaelia Chiron & V. P. Castro, Chironiella Braem, Brasilaelia Campacci, Cattleyella Van den Berg & M. W. Chase, Schluckebieria Braem Caularthron Raf. 3 Syn. Diacrium Benth. Dothilophis Raf. Constantia Barb. Rodr. 5 Dimerandra Schltr. 1 Dinema Lindl. 1 Domingoa Schltr. 5 Syn. Hartwegia Lindl. Nageliella L. O. Williams Encyclia Hook. 120 Epidendrum L. 1500 Syn.
Amblostoma Scheidw. Amblystoma Kuntze, Amphiglottis Salisb. Amphiglottium Lindl. Ex Stein, Auliza Salisb. Auliza Salisb. Ex Small, Aulizeum Lindl. Ex Stein, Coilostylis Raf. Didothion Raf. Diothonea Lindl. Epidanthus L. O. Williams, Epidendropsis Garay & Dunst. Gastropodium Lindl. Hemiscleria Lindl. Kalopternix Garay & Dunst. Lanium Benth. Larnandra Raf. Minicolumna Brieger, Nanodes Lindl. Neohlemannia Kraenzl. Neowilliamsia Garay, Nyctosma Raf. Oerstedella Rchb.f. Physinga Lindl. Pleuranthium Benth. Pseudepidendrum Rchb.f. Psilanthemum Klotszch ex Stein, Seraphyta Fisch. & C. A. Mey. Spathiger Small, Spathium Lindl. Ex Stein, Stenoglossum Kunth, Tritelandra Raf. Guarianthe Dressler & W. E. Higgins, 4 Hagsatera R. González, 2 Homalopetalum Rolfe, 7 Syn. Pinelia Lindl. Pinelianthe Rauschert Isabelia Barb. Rodr. 3 Syn. Neolauchea Kraenzl. Sophronitella Schltr. Jacquiniella Schltr. 11 Syn. Dressleriella Brieger, Briegeria Senghas Laelia Lindl. 25 Syn. Amalia Lindl. Amalias Hofmsgg. Schomburgkia Lindl. Laeliocatarthron Leptotes Lindl. 5 Loefgrenianthus Hoehne, 1 Meiracyllium Rchb.f.
2 Microepidendrum Brieger ex W. E. Higgins, 1 Myrmecophila Rolfe, 10 Nidema Britton & Millsp. 2 Oestlundia W. E. Higgins, 4 Orleanesia Barb. Rodr. 11 Prosthechea Knowles & Westc. 100 Syn. Epithecium Knowles & Westc. Hormidium Heynh. Anacheilium Hoffmgg. Euchile Withner, Pseudencyclia Chiron & V. P. Castro. Panarica Withner & P. A. Harding, Pollardia Withner & P. A. Harding Pseudolaelia Porto & Brade, 10 Syn. Renata Ruschi Psychilis Raf. 15 Pygmaeorchis Brade, 2 Quisqueya Dod, 4 Rhyncholaelia Schltr, 2 Scaphyglottis Poepp. & Endl. 60 Syn. Hexisea Lindl. Cladobium Lindl. Hexadesmia Brongn. Tetragamestus Rchb.f. Reichenbachanthus Barb. Rodr. Fractiungis Schltr. Leaoa Schltr. & Porto, Pachystele Schltr. Costaricaea Schltr. Ramonia Schltr. Platyglottis L. O. Williams Tetramicra Lindl. 13 van den Berg, C. W. E. Higgins, R. L. Dressler, W. M. Whitten, M. A. Soto Arenas, A. Culham and M. W. Chase. 2000. A Phylogenetic Analysis of Laeliinae Based on Sequence Data from Internal Transcribed Spacers of Nuclear Ribosomal DNA. Lindleyana 15: 96–114.
Van den Berg, C. et al. 2005. Subtribe Laeliinae. Pp. 181–316 In Pridgeon, A. M. Cribb, P. J. Chase, M. W. Rasmussen, F. N. Genera Orchidacearum Vol. IV. Oxford University Press, Oxford. Van den Berg C, Chase M. W. 2005 Nomenclatural notes on Laeliinae - IV. New combinations in Sophronitis. Kew Bull. 59.: 565-567 van den Berg, C. 2014. Reaching a compromise between conflicting nuclear and plastid phylogenetic trees: a new classification for the genus Cattleya. Phytotaxa 186: 075–086. Photo album of Laeliinae species and hybrids Checklist of Laeliinae genera
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
In biology, a hybrid is the offspring resulting from combining the qualities of two organisms of different breeds, species or genera through sexual reproduction. Hybrids are not always intermediates between their parents, but can show hybrid vigour, sometimes growing larger or taller than either parent; the concept of a hybrid is interpreted differently in animal and plant breeding, where there is interest in the individual parentage. In genetics, attention is focused on the numbers of chromosomes. In taxonomy, a key question is how related the parent species are. Species are reproductively isolated by strong barriers to hybridisation, which include morphological differences, differing times of fertility, mating behaviors and cues, physiological rejection of sperm cells or the developing embryo; some act before fertilization and others after it. Similar barriers exist in plants, with differences in flowering times, pollen vectors, inhibition of pollen tube growth, somatoplastic sterility, cytoplasmic-genic male sterility and the structure of the chromosomes.
A few animal species and many plant species, are the result of hybrid speciation, including important crop plants such as wheat, where the number of chromosomes has been doubled. Human impact on the environment has resulted in an increase in the interbreeding between regional species, the proliferation of introduced species worldwide has resulted in an increase in hybridisation; this genetic mixing may threaten many species with extinction, while genetic erosion in crop plants may be damaging the gene pools of many species for future breeding. A form of intentional human-mediated hybridisation is the crossing of wild and domesticated species; this is common in modern agriculture. One such flower, Oenothera lamarckiana, was central to early genetics research into mutationism and polyploidy, it is more done in the livestock and pet trades. Human selective breeding of domesticated animals and plants has resulted is the development of distinct breeds. Hybrid humans existed in prehistory. For example and anatomically modern humans are thought to have interbred as as 40,000 years ago.
Mythological hybrids appear in human culture in forms as diverse as the Minotaur, blends of animals and mythical beasts such as centaurs and sphinxes, the Nephilim of the Biblical apocrypha described as the wicked sons of fallen angels and attractive women. The term hybrid is derived from Latin hybrida, used for crosses such as of a tame sow and a wild boar; the term came into popular use in English in the 19th century, though examples of its use have been found from the early 17th century. Conspicuous hybrids are popularly named with portmanteau words, starting in the 1920s with the breeding of tiger–lion hybrids. From the point of view of animal and plant breeders, there are several kinds of hybrid formed from crosses within a species, such as between different breeds. Single cross hybrids result from the cross between two true-breeding organisms which produces an F1 hybrid; the cross between two different homozygous lines produces an F1 hybrid, heterozygous. The F1 generation is phenotypically homogeneous, producing offspring that are all similar to each other.
Double cross hybrids result from the cross between two different F1 hybrids. Three-way cross hybrids result from the cross between an inbred line. Triple cross hybrids result from the crossing of two different three-way cross hybrids. Top cross hybrids result from the crossing of a top quality or pure-bred male and a lower quality female, intended to improve the quality of the offspring, on average. Population hybrids result from the crossing of plants or animals in one population with those of another population; these crosses between different breeds. In horticulture, the term stable hybrid is used to describe an annual plant that, if grown and bred in a small monoculture free of external pollen produces offspring that are "true to type" with respect to phenotype. Hybridisation can occur in the hybrid zones where the geographical ranges of species, subspecies, or distinct genetic lineages overlap. For example, the butterfly Limenitis arthemis has two major subspecies in North America, L. a. arthemis and L. a. astyanax.
The white admiral has a bright, white band on its wings, while the red-spotted purple has cooler blue-green shades. Hybridisation occurs between a narrow area across New England, southern Ontario, the Great Lakes, the "suture region", it is at these regions. Other hybrid zones have formed between described species of animals. From the point of view of genetics, several different kinds of hybrid can be distinguished. A genetic hybrid carries two different alleles of the same gene, where for instance one allele may code for a lighter coat colour than the other. A structural hybrid results from the fusion of gametes that have differing structure in at least one chromosome, as a result of structural abnormalities. A numerical hybrid results from the fusion of gamet
Broughtonia is a genus of orchids native to the Bahamas and the Greater Antilles. The genus is abbreviated Bro in trade journals; as presently constituted, Broughtonia consists of 6 accepted natural species plus one recognized nothospecies. Broughtonia cubensis Cogn. in I. Urban - Cuba Broughtonia domingensis Rolfe - Hispaniola, Mona Island Broughtonia × jamaicensis Sauleda & R. M. Adams - Jamaica Broughtonia lindenii Dressler - Cuba, Bahamas Broughtonia negrilensis Fowlie - Jamaica Broughtonia ortgiesiana Dressler - Cuba Broughtonia sanguinea R. Br. in W. T. Aiton - JamaicaThe haploid chromosome number of one species, B. sanguinea, has been determined as n = 20. Nir, M. Orchidaceae Antillanae, 49-52, 2000
In plant systematics Epidendroideae is a subfamily of the orchid family, Orchidaceae. Epidendroideae is larger than all the other orchid subfamilies together, comprising more than 15,000 species in 576 genera. Most Epidendroid orchids are tropical epiphytes with pseudobulbs. There are, some terrestrials such as Epipactis and a few myco-heterotrophs, which are parasitic upon mycorrhizal fungi, they contain the remaining orchids with a single, fertile anther, fully incumbent to suberect. The anther form arises from early anther bending; the incumbent anther is pointed backward in many genera. Most have hard pollinia, i.e. a mass of waxy pollen or of coherent pollen grains. The pollinia are without; the stigma are three-lobed. The apical part of the middle stigma lobe forms a stipe; the ovary is unilocular. The leaves are distichous or spiraling; the Epidendroideae are difficult to classify. They have been divided in “lower epidendroids” and “higher epidendroids”. Epiphytes are plants which grow on top of other plants.
They are not parasitic. By growing on other plants, the epiphytes can reach to the light better or where they can avoid struggling for light. Many mosses and lichens are epiphytes, as are 10 per cent of all seed plants and ferns. Epiphytes are common in some groups of plants, such as ferns, mosses and algae. Over half of the 20,000 species of orchids are epiphytes. Most epiphytic seed plants and ferns are found in tropical and subtropical rainforests because they need high humidity to survive; the areas which most epiphytes grow are the montane rainforests. Epiphytic orchids are found on many positions of the host tree, depending on species requirements and size, some large species will grow in a fork, whereas some small species scramble through thin branches, other species will climb up the trunk etc. etc. The trees provide many habitats with different conditions of temperature and light. In temperate places, epiphytes are most common in moist forests, such as the rainforests in Queensland. Epiphytes are not adapted to droughts in the same way are other flora, because they don’t have access to the ground, but they still have some mechanisms to help them survive.
Some become dormant for months at a time. They contain absorptive plants that are capable at taking up water when it is available and preventing drought when water is scarcer. CAM can be impeded by higher night-time temperatures, dehydrated tissues, high saturation deficits in the surrounding air, which lower the "stomata conductance" of the epiphytes, reducing the CO2 uptake, which in turn reduces growth and reproduction and induces carbon loss. Higher temperatures, strain on evaporation, contact to light cause CAM-idling, the epiphyte closing its stomata when it becomes stressed, that brings down the range of habitats a species can inhabit. Epiphyte species work biomasses are much more sensitive to different relative moisture levels than other plants; the Epidendroideae subfamily is divided into two clades or subgroups known as the higher epidendroids and the lower epidendroids. The higher epidendroids are monophyletic and polyphyletic; the tribes are listed below: This classification has a rather ephemeral nature and is prone to frequent revision.
Changes are to occur as new morphological and genetic data become available. A phylogenetic analysis of the Orchidaceae - evidence from rbcL nucleotide sequences Orchid Tree: a phylogeny of epiphytes on the tree of life