banner



Trees 300 Million Years Ago

Sixth and last period of the Paleozoic Era 299–252 million years ago

Permian
298.9 ± 0.15 – 251.902 ± 0.024 Ma

PreꞒ

O

Due south

D

C

P

T

J

Chiliad

Pg

N

Chronology
Etymology
Proper name formality Formal
Usage information
Regional usage Global (ICS)
Time scale(s) used ICS Time Scale
Definition
Chronological unit Period
Stratigraphic unit System
Fourth dimension span formality Formal
Lower boundary definition FAD of the Conodont Streptognathodus isolatus within the morphotype Streptognathodus wabaunsensis chronocline.
Lower boundary GSSP Aidaralash, Ural Mountains, Republic of kazakhstan
50°14′45″N 57°53′29″Eastward  /  50.2458°N 57.8914°E  / 50.2458; 57.8914
GSSP ratified 1996[2]
Upper boundary definition FAD of the Conodont Hindeodus parvus.
Upper purlieus GSSP Meishan, Zhejiang, Prc
31°04′47″North 119°42′21″Due east  /  31.0798°North 119.7058°East  / 31.0798; 119.7058
GSSP ratified 2001[iii]

The Permian ( PUR-mee-ən)[4] is a geologic period and stratigraphic arrangement which spans 47 meg years from the terminate of the Carboniferous Menstruum 298.9 1000000 years agone (Mya), to the starting time of the Triassic Period 251.nine Mya. It is the last period of the Paleozoic Era; the following Triassic Period belongs to the Mesozoic Era. The concept of the Permian was introduced in 1841 by geologist Sir Roderick Murchison, who named it subsequently the region of Perm in Russia.[5] [half-dozen] [7] [viii] [9]

The Permian witnessed the diversification of the two groups of amniotes, the synapsids and the sauropsids (reptiles). The world at the fourth dimension was dominated past the supercontinent Pangaea, which had formed due to the collision of Euramerica and Gondwana during the Carboniferous. Pangaea was surrounded by the superocean Panthalassa. The Carboniferous rainforest collapse left backside vast regions of desert within the continental interior.[x] Amniotes, which could better cope with these drier conditions, rose to dominance in place of their amphibian ancestors.

Various authors recognise at to the lowest degree three,[11] and maybe four[12] extinction events in the Permian. The cease of the Early Permian (Cisuralian) saw a major faunal turnover, with nigh lineages of archaic "pelycosaur" synapsids becoming extinct, being replaced by more avant-garde therapsids. The end of the Capitanian Stage of the Permian was marked by the major Capitanian mass extinction event,[13] associated with the eruption of the Emeishan Traps. The Permian (forth with the Paleozoic) ended with the Permian–Triassic extinction result, the largest mass extinction in Earth's history (which is the last of the three or iv crises that occurred in the Permian), in which well-nigh 81% of marine species and seventy% of terrestrial species died out, associated with the eruption of the Siberian Traps. It took well into the Triassic for life to recover from this catastrophe;[14] on land, ecosystems took thirty million years to recover.[xv]

Etymology and history [edit]

Prior to the introduction of the term "Permian", rocks of equivalent age in Germany had been named the Rotliegend and Zechstein, and in United kingdom as the New Ruby-red Sandstone.[16]

The term "Permian" was introduced into geology in 1841 by Sir Roderick Impey Murchison, president of the Geological Gild of London, after all-encompassing Russian explorations undertaken with Édouard de Verneuil in the vicinity of the Ural Mountains in the years 1840 and 1841. Murchison identified "vast series of beds of marl, schist, limestone, sandstone and conglomerate" that succeeded Carboniferous strata in the region.[17] [18] Murchison, in collaboration with Russian geologists,[xix] named the period after the surrounding Russian region and the city of Perm, which itself take their proper noun from the medieval kingdom of Permia that occupied the same region hundreds of years prior, and which at present lies in the Perm Krai of Russia.[twenty] Between 1853 and 1867, Jules Marcou recognised Permian strata in a big area of North America from the Mississippi River to the Colorado River and proposed the proper name "Dyassic", from "Dyas" and "Trias", though Murchison rejected this in 1871.[21] The Permian organisation was controversial for over a century later on its original naming, with the United States Geological Survey until 1941 considering the Permian a subsystem of the Carboniferous equivalent to the Mississippian and Pennsylvanian.[16]

Geology [edit]

The Permian Period is divided into 3 epochs, from oldest to youngest, the Cisuralian, Guadalupian, and Lopingian. Geologists divide the rocks of the Permian into a stratigraphic set of smaller units called stages, each formed during corresponding time intervals called ages. Stages can exist divers globally or regionally. For global stratigraphic correlation, the International Commission on Stratigraphy (ICS) ratify global stages based on a Global Purlieus Stratotype Section and Indicate (GSSP) from a unmarried formation (a stratotype) identifying the lower boundary of the stage. The ages of the Permian, from youngest to oldest, are:[22]

Epoch Stage Lower boundary
(Ma)
Early Triassic Induan 251.902 ±0.024
Lopingian Changhsingian 254.14 ±0.07
Wuchiapingian 259.one ±0.v
Guadalupian Capitanian 265.ane ±0.4
Wordian 268.8 ±0.5
Roadian 272.95 ±0.11
Cisuralian Kungurian 283.v ±0.6
Artinskian 290.1 ±0.26
Sakmarian 293.52 ±0.17
Asselian 298.nine ±0.15

For most of the 20th century, the Permian was divided into the Early and Late Permian, with the Kungurian beingness the last stage of the Early Permian.[23] Glenister and colleagues in 1992 proposed a tripartite scheme, advocating that the Roadian-Capitanian was distinct from the balance of the Late Permian, and should be regarded as a separate epoch.[24] The tripartite split was adopted after a formal proposal by Glenister et al. (1999).[25]

Historically, most marine biostratigraphy of the Permian was based on ammonoids; however, ammonoid localities are rare in Permian stratigraphic sections, and species characterise relatively long periods of time. All GSSPs for the Permian are based effectually the showtime advent datum of specific species of conodont, an enigmatic group of jawless chordates with hard tooth-like oral elements. Conodonts are used equally index fossils for most of the Palaeozoic and the Triassic.[26]

Cisuralian [edit]

The Cisuralian Series is named after the strata exposed on the western slopes of the Ural Mountains in Russia and Khazakhstan. The name was proposed by J. B. Waterhouse in 1982 to comprise the Asselian, Sakmarian, and Artinskian stages. The Kungurian was afterwards added to accommodate to the Russian "Lower Permian". Albert Auguste Cochon de Lapparent in 1900 had proposed the "Uralian Series", but the subsequent inconsistent usage of this term meant that information technology was later on abandoned.[27]

The Asselian was named by the Russian stratigrapher 5.E. Ruzhenchev in 1954, later the Assel River in the southern Ural Mountains. The GSSP for the base of the Asselian is located in the Aidaralash River valley most Aqtöbe, Republic of kazakhstan, which was ratified in 1996. The beginning of the stage is defined by the commencement appearance of Streptognathodus postfusus. [28]

The Sakmarian is named in reference to the Sakmara River in the southern Urals, and was coined by Alexander Karpinsky in 1874. The GSSP for the base of the Sakmarian is located at the Usolka section in the southern Urals, which was ratified in 2018. The GSSP is divers by the first appearance of Sweetognathus binodosus.[29]

The Artinskian was named after the metropolis of Arti in Sverdlovsk Oblast, Russia. It was named by Karpinsky in 1874. The Artinskian currently lacks a defined GSSP.[22] The proposed definition for the base of the Artinskian is the starting time appearance of Sweetognathus aff. S. whitei.[26]

The Kungurian takes its proper noun afterward Kungur, a urban center in Perm Krai. The phase was introduced past Alexandr Antonovich Stukenberg in 1890. The Kungurian currently lacks a defined GSSP.[22] Contempo proposals have suggested the appearance of Neostreptognathodus pnevi as the lower purlieus.[26]

Guadalupian [edit]

The Guadalupian Series is named afterwards the Guadalupe Mountains in Texas and New Mexico, where extensive marine sequences of this age are exposed. It was named by George Herbert Girty in 1902.[30]

The Roadian was named in 1968 in reference to the Road Coulee Member of the Discussion Germination in Texas.[30] The GSSP for the base of the Roadian is located 42.7m above the base of operations of the Cutoff Formation in Stratotype Coulee, Guadalupe Mountains, Texas, and was ratified in 2001. The beginning of the stage is defined past the offset appearance of Jinogondolella nankingensis.[26]

The Wordian was named in reference to the Give-and-take Germination past Johan August Udden in 1916, Glenister and Replenish in 1961 was the commencement publication to use it as a chronostratigraphic term every bit a substage of the Guadalupian Phase.[30] The GSSP for the base of the Wordian is located in Guadalupe Pass, Texas, within the sediments of the Getaway Limestone Member of the Ruby-red Canyon Formation, which was ratified in 2001. The base of the Wordian is defined by the kickoff appearance of the conodont Jinogondolella aserrata. [26]

The Capitanian is named after the Capitan Reef in the Guadalupe Mountains of Texas, named by George Burr Richardson in 1904, and first used in a chronostratigraphic sense by Glenister and Furnish in 1961 as a substage of the Guadalupian Phase.[30] The Captianian was ratified every bit an international phase past the ICS in 2001. The GSSP for the base of the Captianian is located at Nipple Hill in the southeast Guadalupe Mountains of Texas, and was ratified in 2001, the get-go of the stage is defined past the first advent of Jinogondolella postserrata.[26]

Lopingian [edit]

The Lopingian was first introduced by Amadeus William Grabau in 1923 as the "Loping Series" after Leping, Jiangxi, China. Originally used as a lithostraphic unit, T.K. Huang in 1932 raised the Lopingian to a series, including all Permian deposits in South Mainland china that overlie the Maokou Limestone. In 1995, a vote by the Subcommission on Permian Stratigraphy of the ICS adopted the Lopingian as an international standard chronostratigraphic unit of measurement. [31]

The Wuchiapinginan and Changhsingian were outset introduced in 1962, past J. Z. Sheng as the "Wuchiaping Formation" and "Changhsing Formation" inside the Lopingian series. The GSSP for the base of the Wuchiapingian is located at Penglaitan, Guangxi, China and was ratified in 2004. The boundary is defined by the first appearance of Clarkina postbitteri postbitteri [31] The Changhsingian was originally derived from the Changxing Limestone, a geological unit commencement named by the Grabau in 1923, ultimately deriving from Changxing Canton, Zhejiang .The GSSP for the base of the Changhsingian is located 88 cm to a higher place the base of the Changxing Limestone in the Meishan D section, Zhejiang, Mainland china and was ratified in 2005, the boundary is defined by the first appearance of Clarkina wangi. [32]

The GSSP for the base of the Triassic is located at the base of operations of Bed 27c at the Meishan D section, and was ratified in 2001. The GSSP is defined by the first appearance of the conodont Hindeodus parvus.[33]

Regional stages [edit]

The Russian Tatarian Stage includes the Lopingian, Capitanian and part of the Wordian, while the underlying Kazanian includes the rest of the Wordian as well at the Roadian.[23] In North America, the Permian is divided into the Wolfcampian (which includes the Nealian and the Lenoxian stages) corresponding to the Asselian through lower Kungurian; the Leonardian (Hessian and Cathedralian stages) corresponding to the upper Kungurian; the Guadalupian; and the Ochoan, corresponding to the Lopingian.[34] [35]

Paleogeography [edit]

Geography of the Permian world

During the Permian, all the Earth's major landmasses were nerveless into a single supercontinent known as Pangaea, with the microcontinental terranes of Cathaysia to the east. Pangaea straddled the equator and extended toward the poles, with a corresponding event on ocean currents in the single great ocean ("Panthalassa", the "universal sea"), and 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 Body of water to compress. A new body of water was growing on its southern end, the Neotethys Ocean, an sea that would dominate much of the Mesozoic Era.[36] The Central Pangean Mountains, which began forming due to the collision of Laurasia and Gondwana during the Carboniferous, reached their maximum height during the early Permian around 295 million years ago, comparable to the present Himalayas, but became heavily eroded every bit the Permian progressed.[37] The Kazakhstania block collided with Baltica during the Cisuralian, while the N Prc Craton, the S China Block and Indochina fused to each other and Pangea by the stop of the Permian.[38]

Large continental landmass interiors experience climates with extreme variations of heat and cold ("continental climate") and monsoon conditions with highly seasonal rainfall patterns. Deserts seem to have been widespread on Pangaea.[39] Such dry conditions favored gymnosperms, plants with seeds enclosed in a protective cover, over plants such as ferns that disperse spores in a wetter surround. The first modern trees (conifers, ginkgos and cycads) appeared in the Permian.

Iii general areas are especially noted for their extensive Permian deposits—the Ural Mountains (where Perm itself is located), Cathay, and the southwest of North America, including the Texas ruby beds. The Permian Basin in the U.S. states of Texas and New Mexico is so named because information technology has ane of the thickest deposits of Permian rocks in the world.[xl]

Paleoceanography [edit]

Bounding main levels dropped slightly during the earliest Permian (Asselian). The sea level was stable at several tens of metres above nowadays during the Early Permian, but there was a sharp drop beginning during the Roadian, culminating in the lowest sea level of the unabridged Palaeozoic at around nowadays body of water level during the Wuchiapingian, followed by a slight rising during the Changhsingian.[41]

Climate [edit]

At the start of the Permian, the Earth was still in the Late Paleozoic icehouse, which began in the latest Devonian. At the get-go of the Pennsylvanian around 323 1000000 years agone, glaciers began to form around the Due south Pole, which would grow to cover a vast area. This surface area extended from the southern reaches of the Amazon basin and covered large areas of southern Africa, every bit well as virtually of Australia and Antarctica. Cyclothems point that the size of the glaciers were controlled past Milankovitch cycles alike to recent ice ages, with glacial periods and interglacials. The oldest cyclotherms are around 313 million years old while the youngest are around 293 meg years old, corresponding to the coldest role of the Belatedly Paleozoic icehouse. Deep body of water temperatures during this fourth dimension were cold due to the influx of cold bottom waters generated by seasonal melting of the water ice cap. Past 285 million years agone, temperatures warmed and the South Pole ice cap retreated, though glaciers would remain nowadays in the upland regions of eastern Australia, the Transantarctic Mountains, and the mountainous regions of far northern Siberia until the stop of the Permian. The Permian was absurd in comparison to most other geologic time periods, with modest Pole to Equator temperature gradients. This was interrupted by the Emeishan Thermal Circuit in the late part of the Capitanian, effectually 260 million years ago, corresponding to the eruption of the Emeishan Traps. The end of the Permian is marked by the much larger temperature circuit at the Permian-Triassic boundary, corresponding to the eruption of the Siberian Traps, which released more 5 teratonnes of CO2 , more than doubling atmospheric carbon dioxide concentrations.[42]

Life [edit]

Hercosestria cribrosa, a reef-forming productid brachiopod (Middle Permian, Glass Mountains, Texas)

Marine invertebrates [edit]

Permian marine deposits are rich in fossil mollusks, echinoderms, and brachiopods.[43] Brachiopods were highly diverse during the Permian. The extinct club Productida was the predominant grouping of Permian brachiopods, accounting for up to near half of all Permian brachiopod genera.[44] Conodonts experienced their lowest diversity of their entire evolutionary history during the Permian.[45] Amidst ammonoids, Goniatitida were a major group during the Early-Mid Permian, just declined during the Late Permian. Members of the club Prolecanitida were less diverse. The Ceratitida originated from the family unit Daraelitidae inside Prolecanitida during the mid-Permian, and extensively diversified during the Late Permian.[46] Only three families of trilobite are known from the Permian, Proetidae, Brachymetopidae and Phillipsiidae. Diversity, origination and extinction rates during the Early Permian were low. Trilobites underwent a diversification during the Kungurian-Wordian, the terminal in their evolutionary history, before declining during the Late Permian. Past the Changhsingian, just a handful (4-6) genera remained.[47]

Terrestrial biota [edit]

Terrestrial life in the Permian included diverse plants, fungi, arthropods, and various types of tetrapods. The menses saw a massive desert covering the interior of Pangaea. The warm zone spread in the northern hemisphere, where all-encompassing dry desert appeared.[43] The rocks formed at that time were stained red by iron oxides, the event of intense heating by the sun of a surface devoid of vegetation cover. A number of older types of plants and animals died out or became marginal elements.

The Permian began with the Carboniferous flora still flourishing. Nearly the middle of the Permian a major transition in vegetation began. The swamp-loving lycopod copse of the Carboniferous, such as Lepidodendron and Sigillaria, were progressively replaced in the continental interior by the more avant-garde seed ferns and early conifers equally a outcome of the Carboniferous rainforest collapse. At the close of the Permian, lycopod and equisete swamps reminiscent of Carboniferous flora survived merely on a series of equatorial islands in the Paleo-Tethys Ocean that later would become S China.[48]

The Permian saw the radiation of many important conifer groups, including the ancestors of many present-day families. Rich forests were present in many areas, with a various mix of found groups. The southern continent saw extensive seed fern forests of the Glossopteris flora. Oxygen levels were probably high at that place. The ginkgos and cycads also appeared during this period.

Insects [edit]

Insects, which had first appeared and go abundant during the preceding Carboniferous, experienced a dramatic increase in diversification during the Early Permian. Towards the end of the Permian, there was a substantial drib in both origination and extinction rates.[49] The ascendant insects during the Permian Period were early representatives of Paleoptera, Polyneoptera, and Paraneoptera. Palaeodictyopteroidea, which had represented the ascendant group of insects during the Carboniferous, declined during the Permian. This is likely due to competition by Hemiptera, due to their similar mouthparts and therefore ecology. Primitive relatives of damselflies and dragonflies (Meganisoptera), which include the largest flying insects of all time, likewise declined during the Permian.[l] Holometabola, the largest group of modern insects, also diversified during this time.[49] The earliest known beetles, appear at the beginning of the Permian. Early on beetles such as members of Permocupedidae likely xylophagous feeding on decomposable wood. Several lineages, such as Schizophoridae expanded into aquatic habitats by the Late Permian.[51] Members of the modern orders Archostemata and Adephaga are known from the Late Permian.[52] [53] Complex wood wearisome traces found in the Belatedly Permian of China suggest that members of Polyphaga, the most diverse grouping of mod beetles, were also present in the Permian.[54]

Tetrapods [edit]

The terrestrial fossil record of the Permian is patchy and temporally discontinuous. Early Permian records are dominated by equatorial Europe and N America, while those of the Middle and Late Permian are dominated by temperate Karoo Supergroup sediments of South Africa and the Ural region of European Russia.[55] Early Permian terrestrial faunas of North America and Europe were dominated by primitive pelycosaur synapsids including the herbivorous edaphosaurids, and cannibal sphenacodontids, diadectids and amphibians.[56] [57]

Amniotes [edit]

A faunal turnover occurred at the transition between the Cisuralian and Guadalupian, with the decline of amphibians and the replacement of pelycosaurs with more than advanced therapsids.[11] If terrestrial degradation ended around the end of the Cisuralian in North America and began in Russia during the early Guadalupian, a continuous record of the transition is not preserved. Uncertain dating has led to suggestions that there is a global hiatus in the terrestrial fossil tape during the tardily Kungurian and early Roadian, referred to as "Olson'south Gap" that obscures the nature of the transition. Other proposals have suggested that the Due north American and Russian records overlap,[58] [59] with the latest terrestrial North American deposition occurring during the Roadian, suggesting that there was an extinction event, dubbed "Olsons Extinction".[60] The Eye Permian faunas of Southward Africa and Russia are dominated by therapsids, most abundantly by the diverse Dinocephalia. Dinocephalians become extinct at the end of the Middle Permian, during the Capitanian mass extinction result. Late Permian faunas are dominated by avant-garde therapsids such every bit the predatory sabertoothed gorgonopsians and herbivorous beaked dicynodonts, aslope big herbivorous pareiasaur parareptiles.[61] The Archosauromorpha, the group of reptiles that would give rising to the pseudosuchians, dinosaurs, and pterosaurs in the following Triassic, beginning appeared and diversified during the Late Permian, including the first advent of the Archosauriformes during the latest Permian.[62] Cynodonts, the group of therapsids bequeathed to modern mammals, beginning appeared and gained a worldwide distribution during the Late Permian.[63] Another group of therapsids, the therocephalians (such equally Lycosuchus), arose in the Eye Permian.[64] [65] There were no flying vertebrates, though the extinct lizard like reptile family Weigeltisauridae from the Late Permian had extendable wings like modern gliding lizards, and are the oldest known gliding vertebrates.[66]

Synapsids (the group that would later on include mammals) thrived and diversified greatly at this time. Permian synapsids included some large members such as Dimetrodon. The special adaptations of synapsids enabled them to flourish in the drier climate of the Permian and they grew to boss the vertebrates.[56]

Amphibians [edit]

Permian stem-amniotes consisted of temnospondyli, lepospondyli and batrachosaurs. Temnospondyls reached a tiptop of diversity in the Cisuralian, with a substantial decline during the Guadalupian-Lopingian following Olson'south extinction, with the family unit variety dropping below Carboniferous levels.[67]

Embolomeres, a group of aquatic crocodile-similar reptilliomorphs that previously had its last records in the Cisuralian, are now known to have persisted into the Lopingian in Mainland china.[68]

Modernistic amphibians (lissamphibians) are suggested to have originated during Permian, descending from a lineage of dissorophoid temnospondyls.[69]

Fish [edit]

The diversity of fish during the Permian is relatively low compared to the post-obit Triassic. The dominant grouping of bony fishes during the Permian were the "Paleopterygii" a paraphyletic grouping of Actinopterygii that lie exterior of Neopterygii.[70] The earliest unequivocal members of Neopterygii announced during the Early on Triassic, merely a Permian origin is suspected.[71] The diversity of coelacanths is relatively depression throughout the Permian in comparison to other marine fishes, though there is an increase in diversity during the concluding Permian (Changhsingian), corresponding with the highest diverseness in their evolutionary history during the Early Triassic.[seventy] Diversity of freshwater fish faunas was more often than not low and dominated by lungfish and "Paleopterygians".[70] The last common ancestor of all living lungfish is thought to have existed during the Early Permian. Though the fossil record is fragmentary, lungfish announced to take undergone an evolutionary diversification and size increase in freshwater habitats during the Early Permian, just later on declined during the center and belatedly Permian.[72] Permian chondrichthyan faunas are poorly known.[73] Members of the chondrichthyan clade Holocephali, which contains living chimaeras, reached their apex of diversity during the Carboniferous-Permian, the well-nigh famous Permian representative being the "fizz-saw shark" Helicoprion, known for its unusual screw shaped spiral molar whorl in the lower jaw.[74] Hybodonts, a grouping of shark-like chondrichtyans, were widespread and abundant members of marine and freshwater faunas throughout the Permian.[73] [75] Xenacanthiformes, another extinct group of shark-like chondrichtyans, were common in freshwater habitats, and represented the noon predators of freshwater ecosystems.[76]

Flora [edit]

Map of the world at the Carboniferous-Permian boundary, showing the four floristic provinces

Four floristic provinces in the Permian are recognised, the Angaran, Euramerican, Gondwanan, and Cathaysian realms.[77] The Carboniferous Rainforest Collapse would issue in the replacement of lycopsid-dominated forests with tree-fern dominated ones during the belatedly Carboniferous in Euramerica, and result in the differentiation of the Cathaysian floras from those of Euramerica.[77] The Gondwanan floristic region was dominated past Glossopteridales, a group of woody gymnosperm plants, for nigh of the Permian, extending to loftier southern latitudes. The ecology of the most prominent glossopterid, Glossopteris, has been compared to that of bald cypress, living in mires with waterlogged soils.[78] The tree-like calamites, distant relatives of modern horsetails, lived in coal swamps and grew in bamboo-like vertical thickets. A mostly complete specimen of Arthropitys from the Early Permian Chemnitz petrified woods of Germany demonstrates that they had complex branching patterns like to modern angiosperm trees.[79] The oldest likely record of Ginkgoales (the group containing Ginkgo and its close relatives) is Trichopitys heteromorpha from the earliest Permian of French republic.[80] The oldest known fossils definitively assignable to modern cycads are known from the Late Permian.[81] In Cathaysia, where a moisture tropical frost costless climate prevailed, the Noeggerathiales, an extinct group of tree fern-like progymnosperms were a common component of the flora[82] [83] The earliest Permian (~ 298 meg years ago) Cathyasian Wuda Tuff flora, representing a coal swamp community, has an upper canopy consisting of lycopsid tree Sigillaria, with a lower awning consisting of Marattialean tree ferns, and Noeggerathiales.[77] Early on conifers appeared in the Late Carboniferous, represented by primitive walchian conifers, simply were replaced with more than derived voltzialeans during the Permian. Permian conifers were very similar morphologically to their modern counterparts, and were adapted to stressed dry out or seasonally dry out climatic conditions.[79] Bennettitales, which would become on to become in widespread the Mesozoic, beginning appeared during the Cisuralian in China.[84] Lyginopterids, which had declined in the late Pennsylvanian and later have a patchy fossil record, survived into the Belatedly Permian in Cathaysia and equatorial due east Gondwana.[85]

Permian–Triassic extinction upshot [edit]

The Permian–Triassic extinction consequence, labeled "Terminate P" here, is the most significant extinction issue in this plot for marine genera which produce big numbers of fossils

The Permian ended with the most extensive extinction event recorded in paleontology: the Permian–Triassic extinction event. 90 to 95% of marine species became extinct, every bit well as 70% of all land organisms. It is besides the but known mass extinction of insects.[14] [86] Recovery from the Permian–Triassic extinction result was protracted; on land, ecosystems took 30 million years to recover.[15] Trilobites, which had thrived since Cambrian times, finally became extinct earlier the stop of the Permian. Nautiloids, a subclass of cephalopods, surprisingly survived this occurrence.

At that place is bear witness that magma, in the form of overflowing basalt, poured onto the Globe's surface in what is now chosen the Siberian Traps, for thousands of years, contributing to the environmental stress that led to mass extinction. The reduced coastal habitat and highly increased aridity probably also contributed. Based on the amount of lava estimated to have been produced during this flow, the worst-example scenario is the release of plenty carbon dioxide from the eruptions to raise world temperatures 5 degrees Celsius.[87]

Some other hypothesis involves body of water venting of hydrogen sulfide gas. Portions of the deep sea will periodically lose all of its dissolved oxygen allowing bacteria that alive without oxygen to flourish and produce hydrogen sulfide gas. If enough hydrogen sulfide accumulates in an anoxic zone, the gas can rise into the atmosphere. Oxidizing gases in the temper would destroy the toxic gas, only the hydrogen sulfide would soon consume all of the atmospheric gas available. Hydrogen sulfide levels might have increased dramatically over a few hundred years. Models of such an event bespeak that the gas would destroy ozone in the upper atmosphere allowing ultraviolet radiation to kill off species that had survived the toxic gas.[88] There are species that can metabolize hydrogen sulfide.

Another hypothesis builds on the flood basalt eruption theory. An increase in temperature of five degrees Celsius would non exist enough to explain the death of 95% of life. Merely such warming could slowly raise ocean temperatures until frozen marsh gas reservoirs beneath the bounding main floor near coastlines melted, expelling enough methane (among the most strong greenhouse gases) into the atmosphere to raise globe temperatures an additional five degrees Celsius. The frozen methane hypothesis helps explain the increase in carbon-12 levels found midway in the Permian–Triassic boundary layer. Information technology also helps explain why the commencement phase of the layer's extinctions was state-based, the 2nd was marine-based (and starting correct after the increment in C-12 levels), and the tertiary state-based again.[89]

Come across also [edit]

  • List of fossil sites (with link directory)
  • Olson's Extinction
  • List of Permian tetrapods

References [edit]

  1. ^ "Chart/Fourth dimension Scale". www.stratigraphy.org. International Commission on Stratigraphy.
  2. ^ Davydov, Vladimir; Glenister, Brian; Spinosa, Claude; Ritter, Scott; Chernykh, V.; Wardlaw, B.; Snyder, W. (March 1998). "Proposal of Aidaralash equally Global Stratotype Department and Point (GSSP) for base of the Permian Organisation" (PDF). Episodes. 21: 11–xviii. doi:x.18814/epiiugs/1998/v21i1/003 . Retrieved 7 December 2020.
  3. ^ Hongfu, Yin; Kexin, Zhang; Jinnan, Tong; Zunyi, Yang; Shunbao, Wu (June 2001). "The Global Stratotype Department and Betoken (GSSP) of the Permian-Triassic Boundary" (PDF). Episodes. 24 (2): 102–114. doi:10.18814/epiiugs/2001/v24i2/004 . Retrieved eight December 2020.
  4. ^ "Permian". Lexicon.com Entire (Online). n.d.
  5. ^ Olroyd, D.R. (2005). "Famous Geologists: Murchison". In Selley, R.C.; Cocks, L.R.M.; Plimer, I.R. (eds.). Encyclopedia of Geology, volume 2. Amsterdam: Elsevier. p. 213. ISBN0-12-636380-3.
  6. ^ Ogg, J.G.; Ogg, G.; Gradstein, F.Grand. (2016). A Concise Geologic Time Scale: 2016. Amsterdam: Elsevier. p. 115. ISBN978-0-444-63771-0.
  7. ^ Murchison, R.I.; de Verneuil, E.; von Keyserling, A. (1842). On the Geological Structure of the Central and Southern Regions of Russia in Europe, and of the Ural Mountains. London: Richard and John E. Taylor. p. 14. Permian System. (Zechstein of Federal republic of germany — Magnesian limestone of England)—Some introductory remarks explain why the authors have ventured to use a new proper noun in reference to a grouping of rocks which, every bit a whole, they consider to be on the parallel of the Zechstein of Germany and the magnesian limestone of England. They practice so, not merely considering a portion of deposits has long been known past the name "grits of Perm," but because, being enormously developed in the governments of Perm and Orenburg, they there assume a great diversity of lithological features ...
  8. ^ Murchison, R.I.; de Verneuil, E.; von Keyserling, A. (1845). Geology of Russia in Europe and the Ural Mountains. Vol. one: Geology. London: John Murray. pp. 138–139. ...Convincing ourselves in the field, that these strata were and then distinguished as to institute a system, connected with the carboniferous rocks on the one paw, and independent of the Trias on the other, we ventured to designate them by a geographical term, derived from the ancient kingdom of Permia, inside and around whose precincts the necessary evidences had been obtained. ... For these reasons, so, we were led to abandon both the German language and British nomenclature, and to adopt a geographical name, taken from the region in which the beds are loaded with fossils of an independent and intermediary character; and where the order of superposition is clear, the lower strata of the group being seen to rest upon the Carboniferous rocks.
  9. ^ Verneuil, Eastward. (1842). "Correspondance et communications". Bulletin de la Société Géologique de France. 13: 11–xiv. pp. 12–thirteen: Le nom de Système Permien, nom dérivé de l'ancien royaume de Permie, aujourd'hui gouvernement de Perm, donc ce dépôt occupe une large office, semblerait assez lui convener ... [The proper noun of the Permian Organisation, a name derived from the ancient kingdom of Permia, today the Authorities of Perm, of which this eolith occupies a large part, would seem to arrange information technology well enough ...]
  10. ^ Sahney, S., Benton, Thou.J. & Falcon-Lang, H.J. (2010). "Rainforest plummet triggered Pennsylvanian tetrapod diversification in Euramerica". Geology. 38 (12): 1079–1082. Bibcode:2010Geo....38.1079S. doi:10.1130/G31182.one. S2CID 128642769. {{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ a b Didier, Gilles; Laurin, Michel (9 December 2021). "Distributions of extinction times from fossil ages and tree topologies: the instance of mid-Permian synapsid extinctions". PeerJ. 9: e12577. doi:ten.7717/peerj.12577. PMC8667717. PMID 34966586.
  12. ^ Lucas, South.Yard. (July 2017). "Permian tetrapod extinction events". Globe-Science Reviews. 170: 31–sixty. Bibcode:2017ESRv..170...31L. doi:ten.1016/j.earscirev.2017.04.008.
  13. ^ Day, Michael O.; Ramezani, Jahandar; Bowring, Samuel A.; Sadler, Peter G.; Erwin, Douglas H.; Abdala, Fernando; Rubidge, Bruce South. (22 July 2015). "When and how did the terrestrial mid-Permian mass extinction occur? Testify from the tetrapod record of the Karoo Basin, Southward Africa". Proceedings of the Purple Society B: Biological Sciences. 282 (1811): 20150834. doi:10.1098/rspb.2015.0834. PMC4528552. PMID 26156768.
  14. ^ a b "GeoKansas--Geotopics--Mass Extinctions". ku.edu. Archived from the original on 2012-09-twenty. Retrieved 2009-11-05 .
  15. ^ a b Sahney, S.; Benton, M. J. (2008). "Recovery from the most profound mass extinction of all time". Proceedings of the Royal Society B: Biological Sciences. 275 (1636): 759–65. doi:10.1098/rspb.2007.1370. PMC2596898. PMID 18198148.
  16. ^ a b Benton, Michael J.; Sennikov, Andrey G. (2021-06-08). "The naming of the Permian System". Periodical of the Geological Society. 179. doi:10.1144/jgs2021-037. ISSN 0016-7649. S2CID 235773352.
  17. ^ Benton, M.J. et al., Murchison'south start sighting of the Permian, at Vyazniki in 1841 Archived 2012-03-24 at WebCite, Proceedings of the Geologists' Clan, accessed 2012-02-21
  18. ^ Murchison, Roderick Impey (1841) "Beginning sketch of some of the principal results of a 2d geological survey of Russia," Philosophical Magazine and Periodical of Scientific discipline, series three, 19 : 417-422. From p. 419: "The carboniferous arrangement is surmounted, to the east of the Volga, by a vast series of marls, schists, limestones, sandstones and conglomerates, to which I propose to give the proper name of "Permian System," … ."
  19. ^ Henderson, C. 1000.; Davydov and, V. I.; Wardlaw, B. R.; Gradstein, F. K.; Hammer, O. (2012-01-01), Gradstein, Felix M.; Ogg, James G.; Schmitz, Mark D.; Ogg, Gabi M. (eds.), "Affiliate 24 - The Permian Period", The Geologic Fourth dimension Scale, Boston: Elsevier, pp. 653–679, doi:ten.1016/b978-0-444-59425-ix.00024-x, ISBN978-0-444-59425-9 , retrieved 2022-02-01 , In 1841, after a tour of Russia with French paleontologist Edouard de Verneuil, Roderick I. Murchison, in collabo- ration with Russian geologists, named the Permian System
  20. ^ Henderson, C. M.; Davydov and, V. I.; Wardlaw, B. R.; Gradstein, F. 1000.; Hammer, O. (2012-01-01), Gradstein, Felix M.; Ogg, James G.; Schmitz, Marker D.; Ogg, Gabi M. (eds.), "Chapter 24 - The Permian Period", The Geologic Time Scale, Boston: Elsevier, p. 654, doi:10.1016/b978-0-444-59425-9.00024-x, ISBN978-0-444-59425-nine , retrieved 2022-02-01 , He proposed the name "Permian" based on the extensive region that composed the ancient kingdom of Permia; the city of Perm lies on the flanks of the Urals.
  21. ^ Henderson, C.M.; Davydov and, 5.I.; Wardlaw, B.R.; Gradstein, F.Thousand.; Hammer, O. (2012), "The Permian Catamenia", The Geologic Time Scale, Elsevier, pp. 653–679, doi:ten.1016/b978-0-444-59425-nine.00024-ten, ISBN978-0-444-59425-9 , retrieved 2021-03-17
  22. ^ a b c Cohen, K.Yard., Finney, S.C., Gibbard, P.L. & Fan, J.-X. (2013; updated) The ICS International Chronostratigraphic Chart. Episodes 36: 199-204.
  23. ^ a b Olroyd, Savannah Fifty.; Sidor, Christian A. (August 2017). "A review of the Guadalupian (middle Permian) global tetrapod fossil record". Globe-Scientific discipline Reviews. 171: 583–597. Bibcode:2017ESRv..171..583O. doi:ten.1016/j.earscirev.2017.07.001.
  24. ^ Glenister, Brian F.; Boyd, D. Westward.; Furnish, W. M.; Grant, R. E.; Harris, Thousand. T.; Kozur, H.; Lambert, Fifty. L.; Nassichuk, W. West.; Newell, Northward. D.; Pray, L. C.; Spinosa, C. (September 1992). "The Guadalupian: Proposed International Standard for a Centre Permian Series". International Geology Review. 34 (9): 857–888. Bibcode:1992IGRv...34..857G. doi:10.1080/00206819209465642. ISSN 0020-6814.
  25. ^ Glenister BF., Wardlaw BR., Lambert LL., Spinosa C., Bowring SA., Erwin DH., Menning M., Wilde GL. 1999. Proposal of Guadalupian and component Roadian, Wordian and Capitanian stages equally international standards for the middle Permian series. Permophiles 34:3-eleven
  26. ^ a b c d e f Lucas, Spencer G.; Shen, Shu-Zhong (2018). "The Permian timescale: an introduction". Geological Society, London, Special Publications. 450 (1): ane–xix. Bibcode:2018GSLSP.450....1L. doi:10.1144/SP450.xv. ISSN 0305-8719.
  27. ^ Gradstein, Felix Thousand.; Ogg, James G.; Smith, Alan Grand. (2004). A geologic time scale 2004. Cambridge University Press. p. 250. ISBN978-0-521-78673-7.
  28. ^ Davydov, 5.I., Glenister, B.F., Spinosa, C., Ritter, South.M., Chernykh, V.5., Wardlaw, B.R. & Snyder, W.South. 1998. Proposal of Aidaralash equally Global Stratotype Department and Point (GSSP) for base of operations of the Permian Organisation. Episodes, 21, eleven–17.
  29. ^ Chernykh, by Valery V.; Chuvashov, Boris I.; Shen, Shu-Zhong; Henderson, Charles Thousand.; Yuan, Dong-Xun; Stephenson, and Michael H. (2020-12-01). "The Global Stratotype Section and Point (GSSP) for the base- Sakmarian Stage (Cisuralian, Lower Permian)". Episodes. 43 (4): 961–979. doi:x.18814/epiiugs/2020/020059.
  30. ^ a b c d Glenister, B.F., Wardlaw, B.R. et al. 1999. Proposal of Guadalupian and component Roadian, Wordian and Capitanian stages equally international standards for the middle Permian series. Permophiles, 34, iii–11.
  31. ^ a b Jin, Y.; Shen, S.; Henderson, C. Chiliad.; Wang, X.; Wang, W.; Wang, Y.; Cao, C. & Shang, Q.; 2006: The Global Stratotype Section and Indicate (GSSP) for the boundary between the Capitanian and Wuchiapingian Stage (Permian), Episodes 29(4), pp. 253–262
  32. ^ Jin, Yugan; Wang, Yue; Henderson, Charles; Wardlaw, Bruce R.; Shen, Shuzhong; Cao, Changqun (2006-09-01). "The Global Boundary Stratotype Section and Bespeak (GSSP) for the base of Changhsingian Stage (Upper Permian)". Episodes. 29 (3): 175–182. doi:10.18814/epiiugs/2006/v29i3/003. ISSN 0705-3797.
  33. ^ Hongfu, Yin; Kexin, Zhang; Jinnan, Tong; Zunyi, Yang; Shunbao, Wu (June 2001). "The Global Stratotype Section and Point (GSSP) of the Permian-Triassic Boundary" (PDF). Episodes. 24 (2): 102–114. doi:10.18814/epiiugs/2001/v24i2/004 . Retrieved 8 Dec 2020.
  34. ^ Ross, C. A.; Ross, June R. P. (1995). "Permian Sequence Stratigraphy". The Permian of Northern Pangea: 98–123. doi:ten.1007/978-iii-642-78593-1_7. ISBN978-3-642-78595-5.
  35. ^ "Permian: Stratigraphy". UC Museum of Paleontology. University of California Berkeley. Retrieved 17 June 2021.
  36. ^ Scotese, C. R.; Langford, R. P. (1995). "Pangea and the Paleogeography of the Permian". The Permian of Northern Pangea: iii–xix. doi:10.1007/978-three-642-78593-1_1. ISBN978-iii-642-78595-5.
  37. ^ Scotese, C.R.; Schettino, A. (2017), "Late Permian-Early Jurassic Paleogeography of Western Tethys and the Globe", Permo-Triassic Salt Provinces of Europe, North Africa and the Atlantic Margins, Elsevier, pp. 57–95, doi:10.1016/b978-0-12-809417-four.00004-v, ISBN978-0-12-809417-4 , retrieved 2021-03-15
  38. ^ Liu, Jun; Yi, Jian; Chen, Jian-Ye (August 2020). "Constraining assembly time of some blocks on eastern margin of Pangea using Permo-Triassic non-marine tetrapod records". Globe-Scientific discipline Reviews. 207: 103215. Bibcode:2020ESRv..20703215L. doi:10.1016/j.earscirev.2020.103215. S2CID 219766796.
  39. ^ Parrish, J. T. (1995). "Geologic Evidence of Permian Climate". The Permian of Northern Pangea: 53–61. doi:x.1007/978-3-642-78593-1_4. ISBN978-iii-642-78595-5.
  40. ^ Hills, John M. (1972). "Late Paleozoic Sedimentation in Westward Texas Permian Basin". AAPG Message. 56 (12): 2302–2322. doi:10.1306/819A421C-16C5-11D7-8645000102C1865D.
  41. ^ Haq, B. U.; Schutter, S. R. (3 October 2008). "A Chronology of Paleozoic Ocean-Level Changes". Scientific discipline. 322 (5898): 64–68. Bibcode:2008Sci...322...64H. doi:10.1126/science.1161648. PMID 18832639. S2CID 206514545.
  42. ^ Scotese, Christopher R.; Vocal, Haijun; Mills, Benjamin J.W.; van der Meer, Douwe G. (April 2021). "Phanerozoic paleotemperatures: The earth's changing climate during the terminal 540 1000000 years". Earth-Science Reviews. 215: 103503. Bibcode:2021ESRv..21503503S. doi:10.1016/j.earscirev.2021.103503. ISSN 0012-8252. S2CID 233579194. Archived from the original on 7 September 2021. Alt URL
  43. ^ a b "The Permian Catamenia". berkeley.edu.
  44. ^ Carlson, S.J. (2016). "The Evolution of Brachiopoda". Annual Review of Earth and Planetary Sciences. 44: 409–438. Bibcode:2016AREPS..44..409C. doi:ten.1146/annurev-earth-060115-012348.
  45. ^ Ginot, Samuel; Goudemand, Nicolas (December 2020). "Global climate changes account for the chief trends of conodont diversity but non for their last demise". Global and Planetary Change. 195: 103325. Bibcode:2020GPC...19503325G. doi:ten.1016/j.gloplacha.2020.103325. S2CID 225005180.
  46. ^ McGOWAN, Alistair J.; Smith, Andrew B. (May 2007). "Ammonoids Beyond the Permian/Triassic Boundary: A Cladistic Perspective". Palaeontology. fifty (3): 573–590. doi:10.1111/j.1475-4983.2007.00653.x. ISSN 0031-0239.
  47. ^ Lerosey-Aubril, Rudy; Feist, Raimund (2012), Talent, John A. (ed.), "Quantitative Approach to Variety and Refuse in Tardily Palaeozoic Trilobites", World and Life, Dordrecht: Springer Netherlands, pp. 535–555, doi:x.1007/978-90-481-3428-1_16, ISBN978-ninety-481-3427-4 , retrieved 2021-07-25
  48. ^ Xu, R. & Wang, X.-Q. (1982): Di zhi shi qi Zhongguo ge zhu yao Diqu zhi wu jing guan (Reconstructions of Landscapes in Primary Regions of China). Ke xue chu ban she, Beijing. 55 pages, 25 plates.
  49. ^ a b Labandeira, Conrad C. (2018-05-23), "The Fossil History of Insect Diversity", Insect Biodiversity, Chichester, UK: John Wiley & Sons, Ltd, pp. 723–788, doi:10.1002/9781118945582.ch24, ISBN978-1-118-94558-2 , retrieved 2021-07-25
  50. ^ Schachat, Sandra R; Labandeira, Conrad C (2021-03-12). Dyer, Lee (ed.). "Are Insects Heading Toward Their First Mass Extinction? Distinguishing Turnover From Crises in Their Fossil Record". Register of the Entomological Society of America. 114 (2): 99–118. doi:10.1093/aesa/saaa042. ISSN 0013-8746.
  51. ^ Ponomarenko, A. Yard.; Prokin, A. A. (December 2015). "Review of paleontological data on the evolution of aquatic beetles (Coleoptera)". Paleontological Periodical. 49 (thirteen): 1383–1412. doi:10.1134/S0031030115130080. ISSN 0031-0301. S2CID 88456234.
  52. ^ Ponomarenko, A. G.; Volkov, A. N. (November 2013). "Ademosynoides asiaticus Martynov, 1936, the earliest known fellow member of an extant beetle family unit (Insecta, Coleoptera, Trachypachidae)". Paleontological Journal. 47 (6): 601–606. doi:10.1134/s0031030113060063. ISSN 0031-0301. S2CID 84935456.
  53. ^ Yan, Evgeny Viktorovich; Beutel, Rolf Georg; Lawrence, John Francis; Yavorskaya, Margarita Igorevna; Hörnschemeyer, Thomas; Pohl, Hans; Vassilenko, Dmitry Vladimirovich; Bashkuev, Alexey Semenovich; Ponomarenko, Alexander Georgievich (2020-09-thirteen). "Archaeomalthus -(Coleoptera, Archostemata) a 'ghost adult' of Micromalthidae from Upper Permian deposits of Siberia?". Historical Biology. 32 (8): 1019–1027. doi:10.1080/08912963.2018.1561672. ISSN 0891-2963. S2CID 91721262.
  54. ^ Feng, Zhuo; Wang, Jun; Rößler, Ronny; Ślipiński, Adam; Labandeira, Conrad (2017-09-15). "Late Permian wood-borings reveal an intricate network of ecological relationships". Nature Communications. 8 (1): 556. Bibcode:2017NatCo...8..556F. doi:10.1038/s41467-017-00696-0. ISSN 2041-1723. PMC5601472. PMID 28916787.
  55. ^ Brocklehurst, Neil (2020-06-ten). "Olson's Gap or Olson's Extinction? A Bayesian tip-dating arroyo to resolving stratigraphic dubiety". Proceedings of the Royal Order B: Biological Sciences. 287 (1928): 20200154. doi:10.1098/rspb.2020.0154. ISSN 0962-8452. PMC7341920. PMID 32517621.
  56. ^ a b Huttenlocker, A. M., and E. Rega. 2012. The Paleobiology and Bone Microstructure of Pelycosaurian-course Synapsids. Pp. 90–119 in A. Chinsamy (ed.) Forerunners of Mammals: Radiations, Histology, Biology. Indiana University Printing.
  57. ^ "NAPC Abstracts, Sto - Tw". berkeley.edu.
  58. ^ Reisz, Robert R.; Laurin, Michel (i September 2001). <1229:TRMFVE>two.0.CO;ii "The reptile Macroleter: First vertebrate evidence for correlation of Upper Permian continental strata of North America and Russia". GSA Bulletin. 113 (nine): 1229–1233. Bibcode:2001GSAB..113.1229R. doi:10.1130/0016-7606(2001)113<1229:TRMFVE>2.0.CO;2. ISSN 0016-7606.
  59. ^ Brocklehurst, Neil (10 June 2020). "Olson'south Gap or Olson's Extinction? A Bayesian tip-dating approach to resolving stratigraphic doubtfulness". Proceedings of the Royal Society B: Biological Sciences. 287 (1928): 20200154. doi:ten.1098/rspb.2020.0154. PMC7341920. PMID 32517621.
  60. ^ Lucas, S.Yard. (July 2017). "Permian tetrapod extinction events". Earth-Scientific discipline Reviews. 170: 31–sixty. Bibcode:2017ESRv..170...31L. doi:10.1016/j.earscirev.2017.04.008.
  61. ^ Lucas, S.G. (2017-07-01). "Permian tetrapod extinction events". Earth-Science Reviews. 170: 31–60. Bibcode:2017ESRv..170...31L. doi:x.1016/j.earscirev.2017.04.008. ISSN 0012-8252.
  62. ^ Spiekman, Stephan N. F.; Fraser, Nicholas C.; Scheyer, Torsten Yard. (2021-05-03). "A new phylogenetic hypothesis of Tanystropheidae (Diapsida, Archosauromorpha) and other "protorosaurs", and its implications for the early evolution of stem archosaurs". PeerJ. nine: e11143. doi:10.7717/peerj.11143. ISSN 2167-8359. PMC8101476. PMID 33986981.
  63. ^ Huttenlocker, Adam K.; Sidor, Christian A. (2020-12-01). "A Basal Nonmammaliaform Cynodont from the Permian of Republic of zambia and the Origins of Mammalian Endocranial and Postcranial Anatomy". Periodical of Vertebrate Paleontology. twoscore (5): e1827413. doi:10.1080/02724634.2020.1827413. ISSN 0272-4634. S2CID 228883951.
  64. ^ Huttenlocker A. Yard. (2009). "An investigation into the cladistic relationships and monophyly of therocephalian therapsids (Amniota: Synapsida)". Zoological Periodical of the Linnean Society. 157 (4): 865–891. doi:ten.1111/j.1096-3642.2009.00538.10.
  65. ^ Huttenlocker A. K.; Sidor C. A.; Smith R. 1000. H. (2011). "A new specimen of Promoschorhynchus (Therapsida: Therocephalia: Akidnognathidae) from the lowermost Triassic of Southward Africa and its implications for therocephalian survival beyond the Permo-Triassic purlieus". Journal of Vertebrate Paleontology. 31: 405–421. doi:10.1080/02724634.2011.546720. S2CID 129242450.
  66. ^ Pritchard, Adam C.; Sues, Hans-Dieter; Scott, Diane; Reisz, Robert R. (2021-05-20). "Osteology, relationships and functional morphology of Weigeltisaurus jaekeli (Diapsida, Weigeltisauridae) based on a complete skeleton from the Upper Permian Kupferschiefer of Frg". PeerJ. 9: e11413. doi:10.7717/peerj.11413. ISSN 2167-8359. PMC8141288. PMID 34055483.
  67. ^ Ruta, Marcello; Benton, Michael J. (November 2008). "Calibrated Multifariousness, Tree Topology and the Mother of Mass Extinctions: The Lesson of Temnospondyls". Palaeontology. 51 (six): 1261–1288. doi:x.1111/j.1475-4983.2008.00808.x. S2CID 85411546.
  68. ^ Chen, Jianye; Liu, Jun (2020-12-01). "The youngest occurrence of embolomeres (Tetrapoda: Anthracosauria) from the Sunjiagou Formation (Lopingian, Permian) of Due north China". Fossil Tape. 23 (two): 205–213. doi:10.5194/fr-23-205-2020. ISSN 2193-0074.
  69. ^ Schoch, Rainer R. (January 2019). "The putative lissamphibian stem-group: phylogeny and evolution of the dissorophoid temnospondyls". Periodical of Paleontology. 93 (one): 137–156. doi:10.1017/jpa.2018.67. ISSN 0022-3360.
  70. ^ a b c Romano, Carlo; Koot, Martha B.; Kogan, Ilja; Brayard, Arnaud; Minikh, Alla 5.; Brinkmann, Winand; Bucher, Hugo; Kriwet, Jürgen (February 2016). "Permian-Triassic Osteichthyes (bony fishes): diversity dynamics and torso size evolution: Diversity and size of Permian-Triassic bony fishes". Biological Reviews. 91 (one): 106–147. doi:10.1111/brv.12161. PMID 25431138. S2CID 5332637.
  71. ^ Romano, Carlo (2021). "A Hiatus Obscures the Early on Evolution of Modern Lineages of Bony Fishes". Frontiers in Earth Science. viii. doi:10.3389/feart.2020.618853. ISSN 2296-6463.
  72. ^ Kemp, Anne; Cavin, Lionel; Guinot, Guillaume (April 2017). "Evolutionary history of lungfishes with a new phylogeny of post-Devonian genera". Palaeogeography, Palaeoclimatology, Palaeoecology. 471: 209–219. Bibcode:2017PPP...471..209K. doi:10.1016/j.palaeo.2016.12.051.
  73. ^ a b Koot, Martha B.; Cuny, Gilles; Tintori, Andrea; Twitchett, Richard J. (March 2013). "A new various shark fauna from the Wordian (Middle Permian) Khuff Germination in the interior Haushi-Huqf area, Sultanate of Oman: CHONDRICHTHYANS FROM THE WORDIAN KHUFF Germination OF OMAN". Palaeontology. 56 (2): 303–343. doi:10.1111/j.1475-4983.2012.01199.x.
  74. ^ Tapanila, Leif; Pruitt, Jesse; Wilga, Cheryl D.; Pradel, Alan (2020). "Saws, Scissors, and Sharks: Belatedly Paleozoic Experimentation with Symphyseal Dentition". The Anatomical Tape. 303 (ii): 363–376. doi:10.1002/ar.24046. ISSN 1932-8494. PMID 30536888. S2CID 54478736.
  75. ^ Peecook, Brandon R.; Bronson, Allison W.; Otoo, Benjamin K.A.; Sidor, Christian A. (November 2021). "Freshwater fish faunas from two Permian rift valleys of Zambia, novel additions to the ichthyofauna of southern Pangea". Journal of African Earth Sciences. 183: 104325. Bibcode:2021JAfES.18304325P. doi:ten.1016/j.jafrearsci.2021.104325.
  76. ^ Kriwet, Jürgen; Witzmann, Florian; Klug, Stefanie; Heidtke, Ulrich H.J (2008-01-22). "Commencement direct bear witness of a vertebrate three-level trophic chain in the fossil record". Proceedings of the Regal Social club B: Biological Sciences. 275 (1631): 181–186. doi:10.1098/rspb.2007.1170. ISSN 0962-8452. PMC2596183. PMID 17971323.
  77. ^ a b c Wang, J.; Pfefferkorn, H. Due west.; Zhang, Y.; Feng, Z. (2012-03-27). "Permian vegetational Pompeii from Inner Mongolia and its implications for landscape paleoecology and paleobiogeography of Cathaysia". Proceedings of the National Academy of Sciences. 109 (13): 4927–4932. doi:10.1073/pnas.1115076109. ISSN 0027-8424. PMC3323960. PMID 22355112.
  78. ^ McLoughlin, S (2012). "Glossopteris – insights into the compages and relationships of an iconic Permian Gondwanan plant". Journal of the Botanical Society of Bengal. 65 (2): 1–14.
  79. ^ a b Feng, Zhuo (September 2017). "Late Palaeozoic plants". Current Biological science. 27 (17): R905–R909. doi:10.1016/j.cub.2017.07.041. ISSN 0960-9822. PMID 28898663.
  80. ^ Zhou, Zhi-Yan (March 2009). "An overview of fossil Ginkgoales". Palaeoworld. 18 (ane): 1–22. doi:x.1016/j.palwor.2009.01.001.
  81. ^ Feng, Zhuo; Lv, Yong; Guo, Yun; Wei, Hai-Bo; Kerp, Hans (Nov 2017). "Leafage anatomy of a tardily Palaeozoic cycad". Biology Letters. 13 (11): 20170456. doi:10.1098/rsbl.2017.0456. ISSN 1744-9561. PMC5719380. PMID 29093177.
  82. ^ Pfefferkorn, Hermann W.; Wang, Jun (Apr 2016). "Paleoecology of Noeggerathiales, an enigmatic, extinct found grouping of Carboniferous and Permian times". Palaeogeography, Palaeoclimatology, Palaeoecology. 448: 141–150. Bibcode:2016PPP...448..141P. doi:10.1016/j.palaeo.2015.xi.022.
  83. ^ Wang, Jun; Wan, Shan; Kerp, Hans; Bek, Jiří; Wang, Shijun (March 2020). "A whole noeggerathialean plant Tingia unita Wang from the primeval Permian peat-forming flora, Wuda Coalfield, Inner Mongolia". Review of Palaeobotany and Palynology. 294: 104204. doi:10.1016/j.revpalbo.2020.104204. S2CID 216381417.
  84. ^ Blomenkemper, Patrick; Bäumer, Robert; Backer, Malte; Abu Hamad, Abdalla; Wang, Jun; Kerp, Hans; Bomfleur, Benjamin (2021). "Bennettitalean Leaves From the Permian of Equatorial Pangea—The Early Radiation of an Iconic Mesozoic Gymnosperm Group". Frontiers in Earth Science. nine: 162. Bibcode:2021FrEaS...9..162B. doi:10.3389/feart.2021.652699. ISSN 2296-6463.
  85. ^ Zavialova, Natalia; Blomenkemper, Patrick; Kerp, Hans; Hamad, Abdalla Abu; Bomfleur, Benjamin (2021-03-04). "A lyginopterid pollen organ from the upper Permian of the Dead Ocean region". Grana. lx (2): 81–96. doi:x.1080/00173134.2020.1772360. ISSN 0017-3134. S2CID 224931916.
  86. ^ Andrew Alden. "The Great Permian-Triassic Extinction". Most.com Instruction.
  87. ^ Palaeos: Life Through Deep Time > The Permian Flow Archived 2013-06-29 at the Wayback Machine Accessed i April 2013.
  88. ^ Kump, 50.R., A. Pavlov, and One thousand.A. Arthur (2005). "Massive release of hydrogen sulfide to the surface ocean and atmosphere during intervals of oceanic anoxia". Geology. 33 (May): 397–400. Bibcode:2005Geo....33..397K. doi:10.1130/G21295.1. S2CID 34821866. {{cite journal}}: CS1 maint: multiple names: authors list (link)
  89. ^ Benton, Michael J.; Twitchett, Richard J. (vii July 2003). "How to kill (virtually) all life: the end-Permian extinction upshot". Trends in Ecology and Development. 18 (7): 358–365. doi:10.1016/S0169-5347(03)00093-4.

Further reading [edit]

  • Ogg, Jim (June 2004). "Overview of Global Boundary Stratotype Sections and Points (GSSP'south)". stratigraphy.org. Archived from the original on 2004-02-xix. Retrieved Apr 30, 2006.

External links [edit]

  • University of California offers a more mod Permian stratigraphy
  • Classic Permian strata in the Glass Mountains of the Permian Basin
  • "International Commission on Stratigraphy (ICS)". Geologic Time Scale 2004 . Retrieved September 19, 2005.
  • Examples of Permian Fossils
  • Permian (chronostratigraphy calibration)
  • Schneebeli-Hermann, Elke (2012), "Extinguishing a Permian World", Geology, twoscore (three): 287–288, Bibcode:2012Geo....40..287S, doi:10.1130/focus032012.one

Trees 300 Million Years Ago,

Source: https://en.wikipedia.org/wiki/Permian

Posted by: elliottviaguld99.blogspot.com

0 Response to "Trees 300 Million Years Ago"

Post a Comment

Iklan Atas Artikel

Iklan Tengah Artikel 1

Iklan Tengah Artikel 2

Iklan Bawah Artikel