The Permian is a geologic period and system which spans 47 million years from the end of the Carboniferous Period 298.9 million years ago, to the beginning of the Triassic period 251.902 Mya. It is the last period of the Paleozoic era; the concept of the Permian was introduced in 1841 by geologist Sir Roderick Murchison, who named it after the city of Perm. The Permian witnessed the diversification of the early amniotes into the ancestral groups of the mammals, turtles and archosaurs; the world at the time was dominated by two continents known as Pangaea and Siberia, surrounded by a global ocean called Panthalassa. The Carboniferous rainforest collapse left behind vast regions of desert within the continental interior. Amniotes, who could better cope with these drier conditions, rose to dominance in place of their amphibian ancestors; the Permian ended with the Permian–Triassic extinction event, the largest mass extinction in Earth's history, in which nearly 96% of marine species and 70% of terrestrial species died out.
It would take well into the Triassic for life to recover from this catastrophe. Recovery from the Permian–Triassic extinction event was protracted; the term "Permian" was introduced into geology in 1841 by Sir R. I. Murchison, president of the Geological Society of London, who identified typical strata in extensive Russian explorations undertaken with Édouard de Verneuil; the region now lies in the Perm Krai of Russia. Official ICS 2017 subdivisions of the Permian System from most recent to most ancient rock layers are: Lopingian epoch Changhsingian Wuchiapingian Others: Waiitian Makabewan Ochoan Guadalupian epoch Capitanian stage Wordian stage Roadian stage Others: Kazanian or Maokovian Braxtonian stage Cisuralian epoch Kungurian stage Artinskian stage Sakmarian stage Asselian stage Others: Telfordian Mangapirian Sea levels in the Permian remained low, near-shore environments were reduced as all major landmasses collected into a single continent—Pangaea; this could have in part caused the widespread extinctions of marine species at the end of the period by reducing shallow coastal areas preferred by many marine organisms.
During the Permian, all the Earth's major landmasses were collected into a single supercontinent known as Pangaea. Pangaea straddled the equator and extended toward the poles, with a corresponding effect on ocean currents in the single great ocean, the Paleo-Tethys Ocean, a large ocean that existed between Asia and Gondwana; the Cimmeria continent rifted away from Gondwana and drifted north to Laurasia, causing the Paleo-Tethys Ocean to shrink. A new ocean was growing on its southern end, the Tethys Ocean, an ocean that would dominate much of the Mesozoic era. Large continental landmass interiors experience climates with extreme variations of heat and cold and monsoon conditions with seasonal rainfall patterns. Deserts seem to have been widespread on Pangaea; such dry conditions favored gymnosperms, plants with seeds enclosed in a protective cover, over plants such as ferns that disperse spores in a wetter environment. The first modern trees appeared in the Permian. Three general areas are noted for their extensive Permian deposits—the Ural Mountains and the southwest of North America, including the Texas red beds.
The Permian Basin in the U. S. states of Texas and New Mexico is so named because it has one of the thickest deposits of Permian rocks in the world. The climate in the Permian was quite varied. At the start of the Permian, the Earth was still in an ice age. Glaciers receded around the mid-Permian period as the climate warmed, drying the continent's interiors. In the late Permian period, the drying continued although the temperature cycled between warm and cool cycles. Permian marine deposits are rich in fossil mollusks and brachiopods. Fossilized shells of two kinds of invertebrates are used to identify Permian strata and correlate them between sites: fusulinids, a kind of shelled amoeba-like protist, one of the foraminiferans, ammonoids, shelled cephalopods that are distant relatives of the modern nautilus. By the close of the Permian, trilobites and a host of other marine groups became extinct. Terrestrial life in the Permian included diverse plants, fungi and various types of tetrapods; the period saw a massive desert covering the interior of Pangaea.
The warm zone spread in the northern hemisphere. The rocks formed at that time were stained red by iron oxides, the result of intense heating by the sun of a surface devoid of vegetation cover. A number of older types of plants and animals became marginal elements; the Permian began with the Carboniferous flora still flourishing. About the middle of the Permian a major transition in vegetation began; the swamp-loving
The Ordovician is a geologic period and system, the second of six periods of the Paleozoic Era. The Ordovician spans 41.2 million years from the end of the Cambrian Period 485.4 million years ago to the start of the Silurian Period 443.8 Mya. The Ordovician, named after the Celtic tribe of the Ordovices, was defined by Charles Lapworth in 1879 to resolve a dispute between followers of Adam Sedgwick and Roderick Murchison, who were placing the same rock beds in northern Wales into the Cambrian and Silurian systems, respectively. Lapworth recognized that the fossil fauna in the disputed strata were different from those of either the Cambrian or the Silurian systems, placed them in a system of their own; the Ordovician received international approval in 1960, when it was adopted as an official period of the Paleozoic Era by the International Geological Congress. Life continued to flourish during the Ordovician as it did in the earlier Cambrian period, although the end of the period was marked by the Ordovician–Silurian extinction events.
Invertebrates, namely molluscs and arthropods, dominated the oceans. The Great Ordovician Biodiversification Event increased the diversity of life. Fish, the world's first true vertebrates, continued to evolve, those with jaws may have first appeared late in the period. Life had yet to diversify on land. About 100 times as many meteorites struck the Earth per year during the Ordovician compared with today; the Ordovician Period began with a major extinction called the Cambrian–Ordovician extinction event, about 485.4 Mya. It lasted for about 42 million years and ended with the Ordovician–Silurian extinction events, about 443.8 Mya which wiped out 60% of marine genera. The dates given are recent radiometric dates and vary from those found in other sources; this second period of the Paleozoic era created abundant fossils that became major petroleum and gas reservoirs. The boundary chosen for the beginning of both the Ordovician Period and the Tremadocian stage is significant, it correlates well with the occurrence of widespread graptolite and trilobite species.
The base of the Tremadocian allows scientists to relate these species not only to each other, but to species that occur with them in other areas. This makes it easier to place many more species in time relative to the beginning of the Ordovician Period. A number of regional terms have been used to subdivide the Ordovician Period. In 2008, the ICS erected a formal international system of subdivisions. There exist Baltoscandic, Siberian, North American, Chinese Mediterranean and North-Gondwanan regional stratigraphic schemes; the Ordovician Period in Britain was traditionally broken into Early and Late epochs. The corresponding rocks of the Ordovician System are referred to as coming from the Lower, Middle, or Upper part of the column; the faunal stages from youngest to oldest are: Late Ordovician Hirnantian/Gamach Rawtheyan/Richmond Cautleyan/Richmond Pusgillian/Maysville/Richmond Middle Ordovician Trenton Onnian/Maysville/Eden Actonian/Eden Marshbrookian/Sherman Longvillian/Sherman Soudleyan/Kirkfield Harnagian/Rockland Costonian/Black River Chazy Llandeilo Whiterock Llanvirn Early Ordovician Cassinian Arenig/Jefferson/Castleman Tremadoc/Deming/Gaconadian The Tremadoc corresponds to the Tremadocian.
The Floian corresponds to the lower Arenig. The Llanvirn occupies the rest of the Darriwilian, terminates with it at the base of the Late Ordovician; the Sandbian represents the first half of the Caradoc. During the Ordovician, the southern continents were collected into Gondwana. Gondwana started the period in equatorial latitudes and, as the period progressed, drifted toward the South Pole. Early in the Ordovician, the continents of Laurentia and Baltica were still independent continents, but Baltica began to move towards Laurentia in the period, causing the Iapetus Ocean between them to shrink; the small continent Avalonia separated from Gondwana and began to move north towards Baltica and Laurentia, opening the Rheic Ocean between Gondwana and Avalonia. The Taconic orogeny, a major mountain-building episode, was well under way in Cambrian times. In the early and middle Ordovician, temperatures were mild, but at the beginning of the Late Ordovician, from 460 to 450 Ma, volcanoes along the margin of the Iapetus Ocean spewed massive amounts of carbon dioxide, a greenhouse gas, into the atmosphere, turning the planet into a hothouse.
Sea levels were high, but as Gondwana moved south, ice accumulated into glaciers and sea levels dropped. At first, low-lying sea beds increased diversity, but glaciation led to mass extinctions as the seas drained and continental shelves became dry land. During the Ordovician, in fact during the Tremadocian, marine transgressions worldwide were the greatest for which evidence is preserved; these volcanic island arcs collided with proto North America to form the Appalachian mountains. By the end of the Late Ordovician the volcanic emissions had stopped. Gondwana had by that time neared the South Pole and was glaciated
Opisthocoelicaudia is a genus of sauropod dinosaur of the Late Cretaceous Period discovered in the Gobi Desert of Mongolia. The type species is Opisthocoelicaudia skarzynskii. A well-preserved skeleton lacking only the head and neck was unearthed in 1965 by Polish and Mongolian scientists, making Opisthocoelicaudia one of the best known sauropods from the Late Cretaceous. Tooth marks on this skeleton indicate that large carnivorous dinosaurs had fed on the carcass and had carried away the now-missing parts. To date, only two additional, much less complete specimens are known, including a part of a shoulder and a fragmentary tail. A small sauropod, Opisthocoelicaudia measured about 11.4 metres in length. Like other sauropods, it would have been characterised by a small head sitting on a long neck and a barrel shaped trunk carried by four column-like legs; the name Opisthocoelicaudia means "posterior cavity tail", alluding to the unusual, opisthocoel condition of the anterior tail vertebrae that were concave on their posterior sides.
This and other skeletal features lead researchers to propose that Opisthocoelicaudia was able to rear on its hindlegs. Named and described by Polish paleontologist Maria Magdalena Borsuk-Białynicka in 1977, Opisthocoelicaudia was first thought to be a new member of the Camarasauridae, but is considered a derived member of the Titanosauria, its exact relationships within Titanosauria are contentious, but it may have been close to the North American Alamosaurus. All Opisthocoelicaudia fossils stem from the Nemegt Formation. Despite being rich in dinosaur fossils, the only other sauropod from this rock unit is Nemegtosaurus, known from a single skull. Since the skull of Opisthocoelicaudia remains unknown, several researchers have suggested that Nemegtosaurus and Opisthocoelicaudia may represent the same species. Sauropod footprints from the Nemegt Formation, which include skin impressions, can be referred to either Nemegtosaurus or Opisthocoelicaudia as these are the only known sauropods from this formation.
Like other sauropods, Opisthocoelicaudia had a small head on a long neck, a barrel-shaped body on four columnar limbs, a long tail. It was small for a sauropod; the body mass has been estimated at 10.5 t, 22 t, 13 t and 25.4 t in separate studies. The skull and neck are not preserved, but the reconstruction of the nuchal ligament indicates the possession of a neck of medium length of 5 m; as in other titanosaurs, the back was quite flexible due to the lack of accessory vertebral joints, while the pelvic region was strengthened by an additional sixth hip vertebra. The anterior vertebrae of the tail were opisthocoelous, which means they were convex on their anterior sides and concave on their back sides, forming ball-and-socket joints; these opisthocoelous tail vertebrae lend Opisthocoelicaudia its name and serve to distinguish the genus from all other titanosaurs. Other titanosaurs were characterised by procoelous anterior tail vertebrae, which were concave on their anterior sides and convex on their back sides.
Another unique feature can be found in the back vertebrae, which show bifurcated spinous processes, resulting in a double row of bony projections along the top of the spine. While unique in titanosaurs, this feature can be found in several other unrelated sauropods, including Diplodocus and Euhelopus, where it evolved independently; as in the hips of other titanosaurs, the ischium was short, measuring only two-thirds the length of the pubis. The left and right ischium bones as well as the left and right pubis bones were ossified with each other over most of their length, closing the gap that in other sauropods is present between these bones; the limbs were proportionally short. The forelimbs measured 1.87 m in height in the nearly complete specimen two thirds the length of the hindlimbs, which were reconstructed at 2.46 m height. As in other titanosaurs, the limbs were spread outwards rather than standing vertically under the body, while the forelimbs were more flexible and mobile compared to other sauropods.
The manus was composed of the five metacarpalia, which were orientated vertically and arranged in a semicircle. Carpal bones were missing. Finger bones and claws were completely absent – in most other titanosaurs, these bones were still present though reduced in size. In the foot, the talus bone was reduced as in other titanosaurs, while the calcaneus was completely absent in Opisthocoelicaudia. In contrast to the manus, the foot showed well developed claws; the phalangeal formula, which states the number of phalanges beginning with the innermost digit, is 2-2-2-1-0. Foot skeletons of titanosaurs are found, besides Opisthocoelicaudia preserved examples are known only from Epachthosaurus and the unnamed La Invernada titanosaur, whose phalangeal formulas are 2-2-3-2-0 and 2-2-2-2-0, respectively. Of these three titanosaurs, Ophistocoelicaudia was the most derived while showing the fewest phalanges, indicating a progressive reduction in the phalangeal count during titanosaur evolution; the claw of the first digit was not larger than that of the second digit, as in other sauropods, but equal in size.
Osteoderms have been found with at least 10 titanosaur genera. The lack of osteoderms in the nearly complete Opisthocoelicaudia skeleton might indicate that they are absent in this genus. However, the cl
The Cambrian Period was the first geological period of the Paleozoic Era, of the Phanerozoic Eon. The Cambrian lasted 55.6 million years from the end of the preceding Ediacaran Period 541 million years ago to the beginning of the Ordovician Period 485.4 mya. Its subdivisions, its base, are somewhat in flux; the period was established by Adam Sedgwick, who named it after Cambria, the Latin name of Wales, where Britain's Cambrian rocks are best exposed. The Cambrian is unique in its unusually high proportion of lagerstätte sedimentary deposits, sites of exceptional preservation where "soft" parts of organisms are preserved as well as their more resistant shells; as a result, our understanding of the Cambrian biology surpasses that of some periods. The Cambrian marked a profound change in life on Earth. Complex, multicellular organisms became more common in the millions of years preceding the Cambrian, but it was not until this period that mineralized—hence fossilized—organisms became common; the rapid diversification of life forms in the Cambrian, known as the Cambrian explosion, produced the first representatives of all modern animal phyla.
Phylogenetic analysis has supported the view that during the Cambrian radiation, metazoa evolved monophyletically from a single common ancestor: flagellated colonial protists similar to modern choanoflagellates. Although diverse life forms prospered in the oceans, the land is thought to have been comparatively barren—with nothing more complex than a microbial soil crust and a few molluscs that emerged to browse on the microbial biofilm. Most of the continents were dry and rocky due to a lack of vegetation. Shallow seas flanked the margins of several continents created during the breakup of the supercontinent Pannotia; the seas were warm, polar ice was absent for much of the period. Despite the long recognition of its distinction from younger Ordovician rocks and older Precambrian rocks, it was not until 1994 that the Cambrian system/period was internationally ratified; the base of the Cambrian lies atop a complex assemblage of trace fossils known as the Treptichnus pedum assemblage. The use of Treptichnus pedum, a reference ichnofossil to mark the lower boundary of the Cambrian, is difficult since the occurrence of similar trace fossils belonging to the Treptichnids group are found well below the T. pedum in Namibia and Newfoundland, in the western USA.
The stratigraphic range of T. pedum overlaps the range of the Ediacaran fossils in Namibia, in Spain. The Cambrian Period was followed by the Ordovician Period; the Cambrian is divided into ten ages. Only three series and six stages are named and have a GSSP; because the international stratigraphic subdivision is not yet complete, many local subdivisions are still used. In some of these subdivisions the Cambrian is divided into three series with locally differing names – the Early Cambrian, Middle Cambrian and Furongian. Rocks of these epochs are referred to as belonging to Upper Cambrian. Trilobite zones allow biostratigraphic correlation in the Cambrian; each of the local series is divided into several stages. The Cambrian is divided into several regional faunal stages of which the Russian-Kazakhian system is most used in international parlance: *Most Russian paleontologists define the lower boundary of the Cambrian at the base of the Tommotian Stage, characterized by diversification and global distribution of organisms with mineral skeletons and the appearance of the first Archaeocyath bioherms.
The International Commission on Stratigraphy list the Cambrian period as beginning at 541 million years ago and ending at 485.4 million years ago. The lower boundary of the Cambrian was held to represent the first appearance of complex life, represented by trilobites; the recognition of small shelly fossils before the first trilobites, Ediacara biota earlier, led to calls for a more defined base to the Cambrian period. After decades of careful consideration, a continuous sedimentary sequence at Fortune Head, Newfoundland was settled upon as a formal base of the Cambrian period, to be correlated worldwide by the earliest appearance of Treptichnus pedum. Discovery of this fossil a few metres below the GSSP led to the refinement of this statement, it is the T. pedum ichnofossil assemblage, now formally used to correlate the base of the Cambrian. This formal designation allowed radiometric dates to be obtained from samples across the globe that corresponded to the base of the Cambrian. Early dates of 570 million years ago gained favour, though the methods used to obtain this number are now considered to be unsuitable and inaccurate.
A more precise date using modern radiometric dating yield a date of 541 ± 0.3 million years ago. The ash horizon in Oman from which this date was recovered corresponds to a marked fall in the abundance of carbon-13 that correlates to equivalent excursions elsewhere in the world, to the disappearance of distinctive Ediacaran fossils. There are arguments that the dated horizon in Oman does not correspond to the Ediacaran-Cambrian boundary, but represents a facies change from marine to evaporite-dominated strata — which w
Uruguay the Oriental Republic of Uruguay, is a country in the southeastern region of South America. It borders Argentina to its west and Brazil to its north and east, with the Río de la Plata to the south and the Atlantic Ocean to the southeast. Uruguay is home to an estimated 3.44 million people, of whom 1.8 million live in the metropolitan area of its capital and largest city, Montevideo. With an area of 176,000 square kilometres, Uruguay is geographically the second-smallest nation in South America, after Suriname. Uruguay was inhabited by the Charrúa people for 4,000 years before the Portuguese established Colonia del Sacramento in 1680. Montevideo was founded as a military stronghold by the Spanish in the early 18th century, signifying the competing claims over the region. Uruguay won its independence between 1811 and 1828, following a four-way struggle between Spain and Argentina and Brazil, it remained subject to foreign influence and intervention throughout the 19th century, with the military playing a recurring role in domestic politics.
A series of economic crises put an end to a democratic period that had begun in the early 20th century, culminating in a 1973 coup, which established a civic-military dictatorship. The military government persecuted leftists and political opponents, resulting in several deaths and numerous instances of torture by the military. Uruguay is today a democratic constitutional republic, with a president who serves as both head of state and head of government. Uruguay is ranked first in Latin America in democracy, low perception of corruption, e-government, is first in South America when it comes to press freedom, size of the middle class and prosperity. On a per-capita basis, Uruguay contributes more troops to United Nations peacekeeping missions than any other country, it tops the rank of absence of a unique position within South America. It ranks second in the region on economic freedom, income equality, per-capita income and inflows of FDI. Uruguay is the third-best country on the continent in terms of HDI, GDP growth and infrastructure.
It is regarded as a high-income country by the UN. Uruguay was ranked the third-best in the world in e-Participation in 2014. Uruguay is an important global exporter of combed wool, soybeans, frozen beef and milk. Nearly 95% of Uruguay's electricity comes from renewable energy hydroelectric facilities and wind parks. Uruguay is a founding member of the United Nations, OAS, Mercosur, UNASUR and NAM. Uruguay is regarded as one of the most advanced countries in Latin America, it ranks high on global measures of personal rights and inclusion issues. The Economist named Uruguay "country of the year" in 2013, acknowledging the policy of legalizing the production and consumption of cannabis; the name of the namesake river comes from the Spanish pronunciation of the regional Guarani word for it. There are several interpretations, including "bird-river"; the name could refer to a river snail called uruguá, plentiful in the water. In Spanish colonial times, for some time thereafter and some neighbouring territories were called the Cisplatina and Banda Oriental for a few years the "Eastern Province".
Since its independence, the country has been known as la República Oriental del Uruguay, which means "the eastern republic of the Uruguay ". However, it is translated either as the "Oriental Republic of Uruguay" or the "Eastern Republic of Uruguay"; the documented inhabitants of Uruguay before European colonization of the area were the Charrúa, a small tribe driven south by the Guarani of Paraguay. It is estimated that there were about 9,000 Charrúa and 6,000 Chaná and Guaraní at the time of contact with Europeans in the 1500s. Fructuoso Rivera - Uruguay's first president – organized the Charruas' genocide; the Portuguese were the first Europeans to enter the region of present-day Uruguay in 1512. The Spanish arrived in present-day Uruguay in 1516; the indigenous peoples' fierce resistance to conquest, combined with the absence of gold and silver, limited their settlement in the region during the 16th and 17th centuries. Uruguay became a zone of contention between the Spanish and Portuguese empires.
In 1603, the Spanish began to introduce cattle. The first permanent Spanish settlement was founded in 1624 at Soriano on the Río Negro. In 1669–71, the Portuguese built a fort at Colonia del Sacramento. Montevideo was founded by the Spanish in the early 18th century as a military stronghold in the country, its natural harbor soon developed into a commercial area competing with Río de la Plata's capital, Buenos Aires. Uruguay's early 19th century history was shaped by ongoing fights for dominance in the Platine region, between British, Spanish and other colonial forces. In 1806 and 1807, the British army attempted to seize Buenos Aires and Montevideo as part of the Napoleonic Wars. Montevideo was occupied by a British force from February to September 1807. In 1811, José Gervasio Artigas, who became Uruguay's national hero, launched a successful revolt against the Spanish authorities, defeating them on 18 May at the Battle of Las Piedras. In 1813, the new government in Buenos Aires convened a constituent assembly where Artigas emerged as a champ
Dinosaurs are a diverse group of reptiles of the clade Dinosauria. They first appeared during the Triassic period, between 243 and 233.23 million years ago, although the exact origin and timing of the evolution of dinosaurs is the subject of active research. They became the dominant terrestrial vertebrates after the Triassic–Jurassic extinction event 201 million years ago. Reverse genetic engineering and the fossil record both demonstrate that birds are modern feathered dinosaurs, having evolved from earlier theropods during the late Jurassic Period; as such, birds were the only dinosaur lineage to survive the Cretaceous–Paleogene extinction event 66 million years ago. Dinosaurs can therefore be divided into birds; this article deals with non-avian dinosaurs. Dinosaurs are a varied group of animals from taxonomic and ecological standpoints. Birds, at over 10,000 living species, are the most diverse group of vertebrates besides perciform fish. Using fossil evidence, paleontologists have identified over 500 distinct genera and more than 1,000 different species of non-avian dinosaurs.
Dinosaurs are represented on every continent by fossil remains. Through the first half of the 20th century, before birds were recognized to be dinosaurs, most of the scientific community believed dinosaurs to have been sluggish and cold-blooded. Most research conducted since the 1970s, has indicated that all dinosaurs were active animals with elevated metabolisms and numerous adaptations for social interaction; some were herbivorous, others carnivorous. Evidence suggests that egg-laying and nest-building are additional traits shared by all dinosaurs and non-avian alike. While dinosaurs were ancestrally bipedal, many extinct groups included quadrupedal species, some were able to shift between these stances. Elaborate display structures such as horns or crests are common to all dinosaur groups, some extinct groups developed skeletal modifications such as bony armor and spines. While the dinosaurs' modern-day surviving avian lineage are small due to the constraints of flight, many prehistoric dinosaurs were large-bodied—the largest sauropod dinosaurs are estimated to have reached lengths of 39.7 meters and heights of 18 meters and were the largest land animals of all time.
Still, the idea that non-avian dinosaurs were uniformly gigantic is a misconception based in part on preservation bias, as large, sturdy bones are more to last until they are fossilized. Many dinosaurs were quite small: Xixianykus, for example, was only about 50 cm long. Since the first dinosaur fossils were recognized in the early 19th century, mounted fossil dinosaur skeletons have been major attractions at museums around the world, dinosaurs have become an enduring part of world culture; the large sizes of some dinosaur groups, as well as their monstrous and fantastic nature, have ensured dinosaurs' regular appearance in best-selling books and films, such as Jurassic Park. Persistent public enthusiasm for the animals has resulted in significant funding for dinosaur science, new discoveries are covered by the media; the taxon'Dinosauria' was formally named in 1841 by paleontologist Sir Richard Owen, who used it to refer to the "distinct tribe or sub-order of Saurian Reptiles" that were being recognized in England and around the world.
The term is derived from Ancient Greek δεινός, meaning'terrible, potent or fearfully great', σαῦρος, meaning'lizard or reptile'. Though the taxonomic name has been interpreted as a reference to dinosaurs' teeth and other fearsome characteristics, Owen intended it to evoke their size and majesty. Other prehistoric animals, including pterosaurs, ichthyosaurs and Dimetrodon, while popularly conceived of as dinosaurs, are not taxonomically classified as dinosaurs. Pterosaurs are distantly related to dinosaurs; the other groups mentioned are, like dinosaurs and pterosaurs, members of Sauropsida, except Dimetrodon. Under phylogenetic nomenclature, dinosaurs are defined as the group consisting of the most recent common ancestor of Triceratops and Neornithes, all its descendants, it has been suggested that Dinosauria be defined with respect to the MRCA of Megalosaurus and Iguanodon, because these were two of the three genera cited by Richard Owen when he recognized the Dinosauria. Both definitions result in the same set of animals being defined as dinosaurs: "Dinosauria = Ornithischia + Saurischia", encompassing ankylosaurians, ceratopsians, ornithopods and sauropodomorphs.
Birds are now recognized as being the sole surviving lineage of theropod dinosaurs. In traditional taxonomy, birds were considered a separate class that had evolved from dinosaurs, a distinct superorder. However, a majority of contemporary paleontologists concerned with dinosaurs reject the traditional style of classification in favor of phylogenetic taxonomy. Birds are thus considered to be dinosaurs and dinosaurs are, not extinct. Birds are classified as belonging to the subgroup M
In zoological nomenclature, a type species is the species name with which the name of a genus or subgenus is considered to be permanently taxonomically associated, i.e. the species that contains the biological type specimen. A similar concept is used for suprageneric groups called a type genus. In botanical nomenclature, these terms have no formal standing under the code of nomenclature, but are sometimes borrowed from zoological nomenclature. In botany, the type of a genus name is a specimen, the type of a species name; the species name that has that type can be referred to as the type of the genus name. Names of genus and family ranks, the various subdivisions of those ranks, some higher-rank names based on genus names, have such types. In bacteriology, a type species is assigned for each genus; every named genus or subgenus in zoology, whether or not recognized as valid, is theoretically associated with a type species. In practice, there is a backlog of untypified names defined in older publications when it was not required to specify a type.
A type species is both a concept and a practical system, used in the classification and nomenclature of animals. The "type species" represents the reference species and thus "definition" for a particular genus name. Whenever a taxon containing multiple species must be divided into more than one genus, the type species automatically assigns the name of the original taxon to one of the resulting new taxa, the one that includes the type species; the term "type species" is regulated in zoological nomenclature by article 42.3 of the International Code of Zoological Nomenclature, which defines a type species as the name-bearing type of the name of a genus or subgenus. In the Glossary, type species is defined as The nominal species, the name-bearing type of a nominal genus or subgenus; the type species permanently attaches a formal name to a genus by providing just one species within that genus to which the genus name is permanently linked. The species name in turn is fixed, to a type specimen. For example, the type species for the land snail genus Monacha is Helix cartusiana, the name under which the species was first described, known as Monacha cartusiana when placed in the genus Monacha.
That genus is placed within the family Hygromiidae. The type genus for that family is the genus Hygromia; the concept of the type species in zoology was introduced by Pierre André Latreille. The International Code of Zoological Nomenclature states that the original name of the type species should always be cited, it gives an example in Article 67.1. Astacus marinus Fabricius, 1775 was designated as the type species of the genus Homarus, thus giving it the name Homarus marinus. However, the type species of Homarus should always be cited using its original name, i.e. Astacus marinus Fabricius, 1775. Although the International Code of Nomenclature for algae and plants does not contain the same explicit statement, examples make it clear that the original name is used, so that the "type species" of a genus name need not have a name within that genus, thus in Article 10, Ex. 3, the type of the genus name Elodes is quoted as the type of the species name Hypericum aegypticum, not as the type of the species name Elodes aegyptica.
Glossary of scientific naming Genetypes – genetic sequence data from type specimens. Holotype Paratype Principle of Typification Type Type genus