Asparagales is an order of plants in modern classification systems such as the Angiosperm Phylogeny Group and the Angiosperm Phylogeny Web. The order takes its name from the type family Asparagaceae and is placed in the monocots amongst the lilioid monocots; the order has only been recognized in classification systems. It was first put forward by Huber in 1977 and taken up in the Dahlgren system of 1985 and the APG in 1998, 2003 and 2009. Before this, many of its families were assigned to the old order Liliales, a large order containing all monocots with colourful tepals and lacking starch in their endosperm. DNA sequence analysis indicated that many of the taxa included in Liliales should be redistributed over three orders, Liliales and Dioscoreales; the boundaries of the Asparagales and of its families have undergone a series of changes in recent years. In the APG circumscription, Asparagales is the largest order of monocots with 14 families, 1,122 genera, about 36,000 species; the order is circumscribed on the basis of molecular phylogenetics, but is difficult to define morphologically, since its members are structurally diverse.
Most species of Asparagales are herbaceous perennials, although some are climbers and some are tree-like. The order contains many geophytes. According to telomere sequence, at least two evolutionary switch-points happened within the order. Basal sequence is formed by TTTAGGG like in majority of higher plants. Basal motif was changed to vertebrate-like TTAGGG and the most divergent motif CTCGGTTATGGG appears in Allium. One of the defining characteristics of the order is the presence of phytomelanin, a black pigment present in the seed coat, creating a dark crust. Phytomelanin is found in most families of the Asparagales; the leaves of all species form a tight rosette, either at the base of the plant or at the end of the stem, but along the stem. The flowers are not distinctive, being'lily type', with six tepals and up to six stamina; the order is thought to have first diverged from other related monocots some 120–130 million years ago, although given the difficulty in classifying the families involved, estimates are to be uncertain.
From an economic point of view, the order Asparagales is second in importance within the monocots to the order Poales. Species are used as food and flavourings, as cut flowers, as garden ornamentals. Although most species in the order are herbaceous, some no more than 15 cm high, there are a number of climbers, as well as several genera forming trees, which can exceed 10 m in height. Succulent genera occur in several families. All species have a tight cluster of leaves, either at the base of the plant or at the end of a more-or-less woody stem as with Yucca. In some cases the leaves are produced along the stem; the flowers are in the main not distinctive, being of a general'lily type', with six tepals, either free or fused from the base and up to six stamina. They are clustered at the end of the plant stem; the Asparagales are distinguished from the Liliales by the lack of markings on the tepals, the presence of septal nectaries in the ovaries, rather than the bases of the tepals or stamen filaments, the presence of secondary growth.
They are geophytes, but with linear leaves, a lack of fine reticular venation. The seeds characteristically have the external epidermis either obliterated, or if present, have a layer of black carbonaceous phytomelanin in species with dry fruits; the inner part of the seed coat is collapsed, in contrast to Liliales whose seeds have a well developed outer epidermis, lack phytomelanin, display a cellular inner layer. The orders which have been separated from the old Liliales are difficult to characterize. No single morphological character appears to be diagnostic of the order Asparagales; the flowers of Asparagales are of a general type among the lilioid monocots. Compared to Liliales, they have plain tepals without markings in the form of dots. If nectaries are present, they are in the septa of the ovaries rather than at the base of the tepals or stamens; those species which have large dry seeds have a dark, crust-like outer layer containing the pigment phytomelan. However, some species with hairy seeds, berries, or reduced seeds lack this dark pigment in their seed coats.
Phytomelan is not unique to Asparagales but it is common within the order and rare outside it. The inner portion of the seed coat is completely collapsed. In contrast, the morphologically similar seeds of Liliales have no phytomelan, retain a cellular structure in the inner portion of the seed coat. Most monocots are unable to thicken their stems once they have formed, since they lack the cylindrical meristem present in other angiosperm groups. Asparagales have a method of secondary thickening, otherwise only found inDioscorea. In a process called'anomalous secondary growth', they are able to create new
In botany and dendrology, a rhizome is a modified subterranean plant stem that sends out roots and shoots from its nodes. Rhizomes are called creeping rootstalks or just rootstalks. Rhizomes grow horizontally; the rhizome retains the ability to allow new shoots to grow upwards. A rhizome is the main stem of the plant. A stolon is similar to a rhizome, but a stolon sprouts from an existing stem, has long internodes, generates new shoots at the end, such as in the strawberry plant. In general, rhizomes have short internodes, send out roots from the bottom of the nodes, generate new upward-growing shoots from the top of the nodes. A stem tuber is a thickened part of a rhizome or stolon, enlarged for use as a storage organ. In general, a tuber is high in starch, e.g. the potato, a modified stolon. The term "tuber" is used imprecisely and is sometimes applied to plants with rhizomes. If a rhizome is separated each piece may be able to give rise to a new plant; the plant uses the rhizome to store starches and other nutrients.
These nutrients become useful for the plant when new shoots must be formed or when the plant dies back for the winter. This is a process known as vegetative reproduction and is used by farmers and gardeners to propagate certain plants; this allows for lateral spread of grasses like bamboo and bunch grasses. Examples of plants that are propagated this way include hops, ginger, lily of the valley and sympodial orchids; some rhizomes which are used directly in cooking include ginger, galangal and lotus. Stored rhizomes are subject to bacterial and fungal infections, making them unsuitable for replanting and diminishing stocks. However, rhizomes can be produced artificially from tissue cultures; the ability to grow rhizomes from tissue cultures leads to better stocks for replanting and greater yields. The plant hormones ethylene and jasmonic acid have been found to help induce and regulate the growth of rhizomes in rhubarb. Ethylene, applied externally was found to affect internal ethylene levels, allowing easy manipulations of ethylene concentrations.
Knowledge of how to use these hormones to induce rhizome growth could help farmers and biologists producing plants grown from rhizomes more cultivate and grow better plants. Some plants have rhizomes that grow above ground or that lie at the soil surface, including some Iris species, ferns, whose spreading stems are rhizomes. Plants with underground rhizomes include gingers, the Venus flytrap, Chinese lantern, western poison-oak and Alstroemeria, the weeds Johnson grass, Bermuda grass, purple nut sedge. Rhizomes form a single layer, but in giant horsetails, can be multi-tiered. Many rhizomes have culinary value, some, such as zhe'ergen, are consumed raw. Aspen Corm Mycorrhiza Media related to Rhizomes at Wikimedia Commons The Rhizome Collective for sustainable living
Maianthemum is a genus of rhizomatous, perennial flowering plants, native to the understory of woodlands. It is widespread across much of North America and Asia. In the APG III classification system, Maianthemum is placed in the family Asparagaceae, subfamily Nolinoideae; because of genetic similarity, similar fruits, evidence that the 4-tepal species evolved from a 6-tepal species, the genus Smilacina was combined with Maianthemum in the late 20th century. Like many lilioid monocots, both Maianthemum and Smilacina were included in the family Liliaceae; the genus has been placed in the former family Convallariaceae, resembles the related Polygonatum, hence the common name "false Solomon's seal". Flowers have six tepals, reduced to four in M. canadense, M. bifolium and M. dilatatum. Species accepted: Maianthemum amoenum LaFrankie – Honduras, El Salvador, Veracruz Maianthemum atropurpureum LaFrankie – Sichuan, Yunnan Maianthemum bicolor Cubey – Korea Maianthemum bifolium F. W. Schmidt – May lily – northern and central Europe and northern Asia from Spain to Kamchatka.
– Canada mayflower, false lily-of-the-valley – much of USA and Canada Maianthemum comaltepecense Espejo, López-Ferr. & Ceja – Oaxaca Maianthemum dahuricum LaFrankie – Siberia, Russian Far East, Inner Mongolia, Korea Maianthemum dilatatum A. Nelson & J. F. Macbr. – snakeberry, wild lily-of-the-valley – Mongolia, Japan, Russian Far East, Yukon, British Columbia, Idaho, California Maianthemum flexuosum LaFrankie – Chiapas, Central America Maianthemum formosanum LaFrankie – Taiwan Maianthemum forrestii LaFrankie – Yunnan Maianthemum fusciduliflorum S. C. Chen & Kawano – Tibet, Bhutan, Myanmar Maianthemum fuscum LaFrankie – Nepal, Yunnan, Assam, Myanmar Maianthemum gigas LaFrankie – Chiapas, Central America Maianthemum gongshanense H. Li – Yunnan Maianthemum henryi LaFrankie – Vietnam, Tibet, southern China Maianthemum hondoense LaFrankie – Honshu Maianthemum × intermedium Vorosch. – Siberia, Russian Far East Maianthemum japonicum LaFrankie – Russian Far East, Korea, northeastern China Maianthemum lichiangense LaFrankie – Gansu, Sichuan, Yunnan Maianthemum macrophyllum LaFrankie – Veracruz Maianthemum mexicanum García Arév – Durango Maianthemum monteverdense LaFrankie – Nicaragua, Costa Rica Maianthemum nanchuanense H.
Li & J. L. Huang – Sichuan Maianthemum oleraceum LaFrankie – Nepal, Assam, Tibet, Guizhou, Yunnan Maianthemum paludicola LaFrankie – Costa Rica Maianthemum paniculatum LaFrankie – Mexico to Costa Rica Maianthemum purpureum LaFrankie – Tibet, Nepal, Sikkim, Assam Maianthemum racemosum Link – false Solomon's-seal – widespread across forested regions of USA and Canada. C. Chen & Kawano – Sichuan, Hubei Maianthemum szechuanicum H. Li – Sichuan, Yunnan Maianthemum tatsienense LaFrankie – Bhutan, Myanmar, Guangxi, Hubei, Sichuan, Yunnan Maianthemum trifolium Sloboda – three-leaf Solomon's-seal, false mayflower Siberia, Russian Far East, Manchuria, much of Canada and north-central United States Maianthemum tubiferum LaFrankie – Gansu, Qinghai, Sichuan Maianthemum yesoense LaFrankie – Japan Polygonatum
Monocotyledons referred to as monocots, are flowering plants whose seeds contain only one embryonic leaf, or cotyledon. They constitute one of the major groups into which the flowering plants have traditionally been divided, the rest of the flowering plants having two cotyledons and therefore classified as dicotyledons, or dicots. However, molecular phylogenetic research has shown that while the monocots form a monophyletic group or clade, the dicots do not. Monocots have always been recognized as a group, but with various taxonomic ranks and under several different names; the APG III system of 2009 recognises a clade called "monocots" but does not assign it to a taxonomic rank. The monocots include about 60,000 species; the largest family in this group by number of species are the orchids, with more than 20,000 species. About half as many species belong to the true grasses, which are economically the most important family of monocots. In agriculture the majority of the biomass produced; these include not only major grains, but forage grasses, sugar cane, the bamboos.
Other economically important monocot crops include various palms and plantains, gingers and their relatives and cardamom, pineapple, water chestnut, leeks and garlic. Many houseplants are monocot epiphytes. Additionally most of the horticultural bulbs, plants cultivated for their blooms, such as lilies, irises, cannas and tulips, are monocots; the monocots or monocotyledons have, as the name implies, a single cotyledon, or embryonic leaf, in their seeds. This feature was used to contrast the monocots with the dicotyledons or dicots which have two cotyledons. From a diagnostic point of view the number of cotyledons is neither a useful characteristic, nor is it reliable; the single cotyledon is only one of a number of modifications of the body plan of the ancestral monocotyledons, whose adaptive advantages are poorly understood, but may have been related to adaption to aquatic habitats, prior to radiation to terrestrial habitats. Monocots are sufficiently distinctive that there has been disagreement as to membership of this group, despite considerable diversity in terms of external morphology.
However, morphological features that reliably characterise major clades are rare. Thus monocots are distinguishable from other angiosperms both in terms of their uniformity and diversity. On the one hand the organisation of the shoots, leaf structure and floral configuration are more uniform than in the remaining angiosperms, yet within these constraints a wealth of diversity exists, indicating a high degree of evolutionary success. Monocot diversity includes perennial geophytes such as ornamental flowers including and succulent epiphytes, all in the lilioid monocots, major cereal grains in the grass family and forage grasses as well as woody tree-like palm trees, bamboo and bromeliads, bananas and ginger in the commelinid monocots, as well as both emergent and aroids, as well as floating or submerged aquatic plants such as seagrass. Organisation and life formsThe most important distinction is their growth pattern, lacking a lateral meristem that allows for continual growth in diameter with height, therefore this characteristic is a basic limitation in shoot construction.
Although herbaceous, some arboraceous monocots reach great height and mass. The latter include agaves, palms and bamboos; this creates challenges in water transport. Some, such as species of Yucca, develop anomalous secondary growth, while palm trees utilise an anomalous primary growth form described as establishment growth; the axis undergoes primary thickening, that progresses from internode to internode, resulting in a typical inverted conical shape of the basal primary axis. The limited conductivity contributes to limited branching of the stems. Despite these limitations a wide variety of adaptive growth forms has resulted from epiphytic orchids and bromeliads to submarine Alismatales and mycotrophic Burmanniaceae and Triuridaceae. Other forms of adaptation include the climbing vines of Araceae which use negative phototropism to locate host trees, while some palms such as Calamus manan produce the longest shoots in the plant kingdom, up to 185 m long. Other monocots Poales, have adopted a therophyte life form.
LeavesThe cotyledon, the primordial Angiosperm leaf consists of a proximal leaf base or hypophyll and a distal hyperphyll. In monocots the hypophyll tends to be the dominant part in contrast to other angiosperms. From these, considerable diversity arises. Mature monocot leaves are narrow and linear, forming a sheath
In botany, a berry is a fleshy fruit without a stone produced from a single flower containing one ovary. Berries so defined include grapes and tomatoes, as well as cucumbers and bananas, but exclude certain fruits called berries, such as strawberries and raspberries; the berry is the most common type of fleshy fruit in which the entire outer layer of the ovary wall ripens into a edible "pericarp". Berries may be formed from one or more carpels from the same flower; the seeds are embedded in the fleshy interior of the ovary, but there are some non-fleshy exceptions, such as peppers, with air rather than pulp around their seeds. Many berries are edible, but others, such as the fruits of the potato and the deadly nightshade, are poisonous to humans. A plant that bears berries is said to be baccate. In everyday English, a "berry" is any small edible fruit. Berries are juicy, brightly coloured, sweet or sour, do not have a stone or pit, although many pips or seeds may be present. In botanical language, a berry is a simple fruit having seeds and fleshy pulp produced from the ovary of a single flower.
The ovary can be superior. It is indehiscent, i.e. it does not have a special "line of weakness" along which it splits to release the seeds when ripe. The pericarp is divided into three layers; the outer layer is called the "exocarp" or "epicarp". Botanists have not applied these terms consistently. Exocarp and endocarp may be restricted to more-or-less single-layered "skins", or may include tissues adjacent to them; the inconsistency in usage has been described as "a source of confusion". The nature of the endocarp distinguishes a berry from a drupe, which has a hardened or stony endocarp; the two kinds of fruit intergrade, depending on the state of the endocarp. Some sources have attempted to quantify the difference, e.g. requiring the endocarp to be less than 2 mm thick in a berry. Examples of botanical berries include: "True berries", or "baccae", may be required to have a thin outer skin, not self-supporting when removed from the berry; this distinguishes, for example, a Vaccinium or Solanum berry from an Adansonia amphisarca, which has a dry, more rigid and self-supporting skin.
The fruit of citrus, such as the orange and lemon, is a berry with a thick rind and a juicy interior divided into segments by septa, given the special name "hesperidium". A specialized term, pepo, is used for fruits of the gourd family Cucurbitaceae, which are modified to have a hard outer rind, but are not internally divided by septae; the fruits of Passiflora and Carica are sometimes considered pepos. Berries that develop from an inferior ovary are sometimes termed epigynous berries or false berries, as opposed to true berries, which develop from a superior ovary. In epigynous berries, the berry includes tissue derived from parts of the flower besides the ovary; the floral tube, formed from the basal part of the sepals and stamens can become fleshy at maturity and is united with the ovary to form the fruit. Common fruits that are sometimes classified as epigynous berries include bananas, members of the genus Vaccinium, members of the family Cucurbitaceae. Many fruits referred to as berries are not actual berries by the scientific definition, but fall into one of the following categories: Drupes are fleshy fruits produced from a single-seeded ovary with a hard woody layer surrounding the seed.
Familiar examples include the stonefruits of the genus Prunus, coconut and Persea species. Some definitions make the mere presence of an internally differentiated endocarp the defining feature of a drupe; the term "drupaceous" is used of fruits that have the general structure and texture of a drupe, without meeting the full definition. Other drupe-like fruits with a single seed that lack the stony endocarp include sea-buckthorn, an achene, surrounded by a swollen hypanthium that provides the fleshy layer. Fruits of Coffea species are described as either berries; the pome fruits produced by plants in subtribe Pyrinae of family Rosaceae, such as apples and pears, have a structure in which tough tissue separates the seeds from the outer softer pericarp. However, some of the smaller pomes are sometimes referred to as berries. Amelanchier pomes become so soft at maturity that they resemble a blueberry and are known as Juneberries, serviceberries or Saskatoon berries. Aggregate or compound fruits contain seeds from different ovaries of a single flower, with the individual "fruitlets" joined together at maturity to form the complete fruit.
Examples of aggregate fruits called "berries" include members of the genus Rubus, such as blackberry and raspberry. Other large aggregate fruits, such as soursop, are not called "berries", although some sources do use this term. Multiple fruits are the fruits of two or more multiple flowers that are merged or packed together; the mulberry is a berry-like example of a multiple fruit.
A leaf is an organ of a vascular plant and is the principal lateral appendage of the stem. The leaves and stem together form the shoot. Leaves are collectively referred to as foliage, as in "autumn foliage". A leaf is a thin, dorsiventrally flattened organ borne above ground and specialized for photosynthesis. In most leaves, the primary photosynthetic tissue, the palisade mesophyll, is located on the upper side of the blade or lamina of the leaf but in some species, including the mature foliage of Eucalyptus, palisade mesophyll is present on both sides and the leaves are said to be isobilateral. Most leaves have distinct upper surface and lower surface that differ in colour, the number of stomata, the amount and structure of epicuticular wax and other features. Leaves can have many different shapes and textures; the broad, flat leaves with complex venation of flowering plants are known as megaphylls and the species that bear them, the majority, as broad-leaved or megaphyllous plants. In the clubmosses, with different evolutionary origins, the leaves are simple and are known as microphylls.
Some leaves, such as bulb scales, are not above ground. In many aquatic species the leaves are submerged in water. Succulent plants have thick juicy leaves, but some leaves are without major photosynthetic function and may be dead at maturity, as in some cataphylls and spines. Furthermore, several kinds of leaf-like structures found in vascular plants are not homologous with them. Examples include flattened plant stems called phylloclades and cladodes, flattened leaf stems called phyllodes which differ from leaves both in their structure and origin; some structures of non-vascular plants function much like leaves. Examples include the phyllids of liverworts. Leaves are the most important organs of most vascular plants. Green plants are autotrophic, meaning that they do not obtain food from other living things but instead create their own food by photosynthesis, they capture the energy in sunlight and use it to make simple sugars, such as glucose and sucrose, from carbon dioxide and water. The sugars are stored as starch, further processed by chemical synthesis into more complex organic molecules such as proteins or cellulose, the basic structural material in plant cell walls, or metabolised by cellular respiration to provide chemical energy to run cellular processes.
The leaves draw water from the ground in the transpiration stream through a vascular conducting system known as xylem and obtain carbon dioxide from the atmosphere by diffusion through openings called stomata in the outer covering layer of the leaf, while leaves are orientated to maximise their exposure to sunlight. Once sugar has been synthesized, it needs to be transported to areas of active growth such as the plant shoots and roots. Vascular plants transport sucrose in a special tissue called the phloem; the phloem and xylem are parallel to each other but the transport of materials is in opposite directions. Within the leaf these vascular systems branch to form veins which supply as much of the leaf as possible, ensuring that cells carrying out photosynthesis are close to the transportation system. Leaves are broad and thin, thereby maximising the surface area directly exposed to light and enabling the light to penetrate the tissues and reach the chloroplasts, thus promoting photosynthesis.
They are arranged on the plant so as to expose their surfaces to light as efficiently as possible without shading each other, but there are many exceptions and complications. For instance plants adapted to windy conditions may have pendent leaves, such as in many willows and eucalyptss; the flat, or laminar, shape maximises thermal contact with the surrounding air, promoting cooling. Functionally, in addition to carrying out photosynthesis, the leaf is the principal site of transpiration, providing the energy required to draw the transpiration stream up from the roots, guttation. Many gymnosperms have thin needle-like or scale-like leaves that can be advantageous in cold climates with frequent snow and frost; these are interpreted as reduced from megaphyllous leaves of their Devonian ancestors. Some leaf forms are adapted to modulate the amount of light they absorb to avoid or mitigate excessive heat, ultraviolet damage, or desiccation, or to sacrifice light-absorption efficiency in favour of protection from herbivory.
For xerophytes the major constraint drought. Some window plants such as Fenestraria species and some Haworthia species such as Haworthia tesselata and Haworthia truncata are examples of xerophytes. and Bulbine mesembryanthemoides. Leaves function to store chemical energy and water and may become specialised organs serving other functions, such as tendrils of peas and other legumes, the protective spines of cacti and the insect traps in carnivorous plants such as Nepenthes and Sarracenia. Leaves are the fundamental structural units from which cones are constructed in gymnosperms and from which flowers are constructed in flowering plants; the internal organisation of most kinds of leaves has evolved to maximise exposure of the photosynthetic organelles, the chloroplasts, to light and to increase the absorption of carbon dioxide while at the same time controlling water loss. Their surfaces are waterproofed by the plant cuticle and gas exchange between the mesophyll cells and the atmosphere is controlled by minute openings called stomata which open or close to regulate the rate exchange of carbon dioxide and water vapour into
Europe is a continent located in the Northern Hemisphere and in the Eastern Hemisphere. It is bordered by the Arctic Ocean to the north, the Atlantic Ocean to the west and the Mediterranean Sea to the south, it comprises the westernmost part of Eurasia. Since around 1850, Europe is most considered to be separated from Asia by the watershed divides of the Ural and Caucasus Mountains, the Ural River, the Caspian and Black Seas and the waterways of the Turkish Straits. Although the term "continent" implies physical geography, the land border is somewhat arbitrary and has been redefined several times since its first conception in classical antiquity; the division of Eurasia into two continents reflects East-West cultural and ethnic differences which vary on a spectrum rather than with a sharp dividing line. The geographic border does not follow political boundaries, with Turkey and Kazakhstan being transcontinental countries. A strict application of the Caucasus Mountains boundary places two comparatively small countries and Georgia, in both continents.
Europe covers 2 % of the Earth's surface. Politically, Europe is divided into about fifty sovereign states of which the Russian Federation is the largest and most populous, spanning 39% of the continent and comprising 15% of its population. Europe had a total population of about 741 million as of 2016; the European climate is affected by warm Atlantic currents that temper winters and summers on much of the continent at latitudes along which the climate in Asia and North America is severe. Further from the sea, seasonal differences are more noticeable than close to the coast. Europe, in particular ancient Greece, was the birthplace of Western civilization; the fall of the Western Roman Empire in 476 AD and the subsequent Migration Period marked the end of ancient history and the beginning of the Middle Ages. Renaissance humanism, exploration and science led to the modern era. Since the Age of Discovery started by Portugal and Spain, Europe played a predominant role in global affairs. Between the 16th and 20th centuries, European powers controlled at various times the Americas all of Africa and Oceania and the majority of Asia.
The Age of Enlightenment, the subsequent French Revolution and the Napoleonic Wars shaped the continent culturally and economically from the end of the 17th century until the first half of the 19th century. The Industrial Revolution, which began in Great Britain at the end of the 18th century, gave rise to radical economic and social change in Western Europe and the wider world. Both world wars took place for the most part in Europe, contributing to a decline in Western European dominance in world affairs by the mid-20th century as the Soviet Union and the United States took prominence. During the Cold War, Europe was divided along the Iron Curtain between NATO in the West and the Warsaw Pact in the East, until the revolutions of 1989 and fall of the Berlin Wall. In 1949 the Council of Europe was founded, following a speech by Sir Winston Churchill, with the idea of unifying Europe to achieve common goals, it includes all European states except for Belarus and Vatican City. Further European integration by some states led to the formation of the European Union, a separate political entity that lies between a confederation and a federation.
The EU originated in Western Europe but has been expanding eastward since the fall of the Soviet Union in 1991. The currency of most countries of the European Union, the euro, is the most used among Europeans. In classical Greek mythology, Europa was a Phoenician princess; the word Europe is derived from her name. The name contains the elements εὐρύς, "wide, broad" and ὤψ "eye, countenance", hence their composite Eurṓpē would mean "wide-gazing" or "broad of aspect". Broad has been an epithet of Earth herself in the reconstructed Proto-Indo-European religion and the poetry devoted to it. There have been attempts to connect Eurṓpē to a Semitic term for "west", this being either Akkadian erebu meaning "to go down, set" or Phoenician'ereb "evening, west", at the origin of Arabic Maghreb and Hebrew ma'arav. Michael A. Barry, professor in Princeton University's Near Eastern Studies Department, finds the mention of the word Ereb on an Assyrian stele with the meaning of "night, sunset", in opposition to Asu " sunrise", i.e. Asia.
The same naming motive according to "cartographic convention" appears in Greek Ἀνατολή. Martin Litchfield West stated that "phonologically, the match between Europa's name and any form of the Semitic word is poor." Next to these hypotheses there is a Proto-Indo-European root *h1regʷos, meaning "darkness", which produced Greek Erebus. Most major world languages use words derived from Europa to refer to the continent. Chinese, for example, uses the word Ōuzhōu. In some Turkic languages the Persian name Frangistan is used casually in referring to much of Europe, besides official names such as Avrupa or Evropa; the prevalent definition of Europe as a geographical term has been in use since the mid-19th century. Europe is taken to be bounded by large bodies of water