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The Triassic ( / t r aɪ ˈ æ s ɪ k / try- ASS -ik ; sometimes symbolized 🝈 ) is a geologic period and system which spans 50.5 million years from the end of the Permian Period 251.902 million years ago ( Mya ), to the beginning of the Jurassic Period 201.4 Mya. The Triassic is the first and shortest period of the Mesozoic Era and the seventh period of the Phanerozoic Eon . Both the start and end of the period are marked by major extinction events . The Triassic Period is subdivided into three epochs: Early Triassic , Middle Triassic and Late Triassic .

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93-464: Rauisuchidae is a group of large (up to 6 metres (20 ft)) predatory Triassic archosaurs . Some disagreement exists over which genera should be included in the Rauisuchidae and which should be in the related Prestosuchidae and Poposauridae , and indeed whether these should even be thought of as separate valid families . Rauisuchidae in the modern sense was defined by Sterling Nesbitt in 2011 as

186-612: A bolide impact, for which an impact crater containing Manicouagan Reservoir in Quebec , Canada , has been singled out. However, the Manicouagan impact melt has been dated to 214±1 Mya. The date of the Triassic-Jurassic boundary has also been more accurately fixed recently, at 201.4 Mya. Both dates are gaining accuracy by using more accurate forms of radiometric dating, in particular the decay of uranium to lead in zircons formed at time of

279-607: A cosmopolitan distribution . Coelacanths show their highest post- Devonian diversity in the Early Triassic . Ray-finned fishes (actinopterygians) went through a remarkable diversification in the beginning of the Triassic, leading to peak diversity during the Middle Triassic; however, the pattern of this diversification is still not well understood due to a taphonomic megabias . The first stem-group teleosts appeared during

372-494: A branch-based clade, Pseudosuchia is the sister taxon of another branch-based clade, the Avemetatarsalia . Avemetatarsalians are bird-line archosaurs, including pterosaurs and dinosaurs (the latter including birds). A different definition was suggested by Benton and Clark, 1988: the node-based taxon including the last common ancestor of Rauisuchidae and aetosaurs and all of its descendants. Benton and Clark also named

465-548: A chain of mountain ranges stretching from Turkey to Malaysia . Pangaea was fractured by widespread faulting and rift basins during the Triassic—especially late in that period—but had not yet separated. The first nonmarine sediments in the rift that marks the initial break-up of Pangaea, which separated eastern North America from Morocco , are of Late Triassic age; in the United States , these thick sediments comprise

558-570: A diverse array of lifestyles during the Jurassic and Cretaceous periods, although only a single subset of crocodylomorphs, the Crocodilia, survive to the present day. Living crocodilians include crocodiles , alligators , caimans , and gavialids . The name Pseudosuchia was originally given to a group of superficially crocodile-like prehistoric reptiles from the Triassic period, but fell out of use in

651-466: A few exposures in the west. During the Triassic peneplains are thought to have formed in what is now Norway and southern Sweden. Remnants of this peneplain can be traced as a tilted summit accordance in the Swedish West Coast . In northern Norway Triassic peneplains may have been buried in sediments to be then re-exposed as coastal plains called strandflats . Dating of illite clay from

744-513: A group called Crocodylotarsi, which includes most taxa now considered pseudosuchians. In 1990, Paul Sereno erected the clade Crurotarsi to supplant Pseudosuchia. However, Sereno defined Crurotarsi as a node-based clade, relying on the inclusion of groups such as Phytosauria , Aetosauria, and Crocodylomorpha . It is not equivalent to Pseudosuchia, which by definition must include all crocodilian-line archosaurs. For many years, Pseudosuchia and Crurotarsi have been considered partial synonyms because

837-860: A later study found that Batrachotomus was a more basal pseudosuchian only slightly more "advanced" than Prestosuchus . In addition, the toothless Lotosaurus has been found to be more closely related to the Ctenosauriscidae , a clade of poposauroids with sails on their backs. Two genera, previously classified as poposaurids, are in fact rauisuchids. These include Teratosaurus and Postosuchus . Arganasuchus ? Fenhosuchus ? Jushatyria ? Polonosuchus Postosuchus Newark Supergroup Procerosuchus ? Rauisuchus Teratosaurus Rhaetian Tikisuchus ? Vivaron Vjushkovisaurus ? Vytshegdosuchus ? [REDACTED] [REDACTED] [REDACTED] [REDACTED] Triassic The Triassic began in

930-471: A long beak-like snout), and Shringasaurus (a horned herbivore which reached a body length of 3–4 metres (9.8–13.1 ft)). One group of archosauromorphs, the archosauriforms , were distinguished by their active predatory lifestyle, with serrated teeth and upright limb postures. Archosauriforms were diverse in the Triassic, including various terrestrial and semiaquatic predators of all shapes and sizes. The large-headed and robust erythrosuchids were among

1023-610: A pseudosuchian. Pseudosuchians were far more ecologically dominant in the Triassic, including large herbivores (such as aetosaurs ), large carnivores (" rauisuchians "), and the first crocodylomorphs (" sphenosuchians "). Aetosaurs were heavily-armored reptiles that were common during the last 30 million years of the Late Triassic until they died out at the Triassic-Jurassic extinction. Most aetosaurs were herbivorous and fed on low-growing plants, but some may have eaten meat. " rauisuchians " (formally known as paracrocodylomorphs ) were

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1116-458: A short period of time, becoming extinct about 220 million years ago. They were exceptionally abundant in the middle of the Triassic, as the primary large herbivores in many Carnian-age ecosystems. They sheared plants with premaxillary beaks and plates along the upper jaw with multiple rows of teeth. Allokotosaurs were iguana-like reptiles, including Trilophosaurus (a common Late Triassic reptile with three-crowned teeth), Teraterpeton (which had

1209-407: A similar definition, Crocodylotarsi, was named in 1988, possibly as a replacement for Pseudosuchia. The name Pseudosuchia, meaning "false crocodiles", has been used for over a century, and traditionally included only non-crocodilians, but when defined as a clade, Pseudosuchia came to include the group Eusuchia ("true crocodiles") as well. Crocodylotarsi may have been named to remove confusion, but as

1302-410: A staggering diversity of reptiles with many different lifestyles. Early pseudosuchians were successful in the Triassic period. They included giant, quadrupedal apex predators such as Saurosuchus , Prestosuchus , and Fasolasuchus . Ornithosuchids were large scavengers, while erpetosuchids and gracilisuchids were small, light-footed predators. A few groups acquired herbivorous diets, such as

1395-399: A stem-based clade, it is synonymous with Pseudosuchia. Because Pseudosuchia was named first, it has precedence. A third group, Crurotarsi , traditionally included the same archosaurs as Pseudosuchia, but as a node-based clade it is not synonymous. The scope of Crurotarsi has recently been changed by the phylogenetic placement of phytosaurs. In 2011, Sterling J. Nesbitt found phytosaurs to be

1488-449: A strandflat of Bømlo , southern Norway, have shown that landscape there became weathered in Late Triassic times ( c. 210 million years ago) with the landscape likely also being shaped during that time. Eustatic sea level in the Triassic was consistently low compared to the other geological periods. The beginning of the Triassic was around present sea level, rising to about 10–20 metres (33–66 ft) above present-day sea level during

1581-570: A supercontinent has less shoreline compared to a series of smaller continents, Triassic marine deposits are relatively uncommon on a global scale. A major exception is in Western Europe , where the Triassic was first studied. The northeastern margin of Gondwana was a stable passive margin along the Neo-Tethys Ocean, and marine sediments have been preserved in parts of northern India and Arabia . In North America , marine deposits are limited to

1674-966: Is a cladogram modified from Nesbitt (2011) showing the new changes (bold terminal taxa are collapsed). † Proterosuchidae [REDACTED] † Erythrosuchus [REDACTED] † Vancleavea [REDACTED] † Proterochampsia [REDACTED] † Euparkeria [REDACTED] † Phytosauria [REDACTED] Avemetatarsalia (bird-lineage of archosaurs) [REDACTED] † Ornithosuchidae [REDACTED] † Gracilisuchus [REDACTED] † Turfanosuchus [REDACTED] † Revueltosaurus [REDACTED] † Aetosauria [REDACTED] † Ticinosuchus [REDACTED] † Poposauroidea [REDACTED] † Prestosuchus [REDACTED] † Saurosuchus [REDACTED] † Batrachotomus [REDACTED] † Fasolasuchus † Rauisuchidae [REDACTED] Crocodylomorpha [REDACTED] The following cladogram

1767-460: Is a recent study of North American faunas. In the Petrified Forest of northeast Arizona there is a unique sequence of late Carnian-early Norian terrestrial sediments. An analysis in 2002 found no significant change in the paleoenvironment. Phytosaurs , the most common fossils there, experienced a change-over only at the genus level, and the number of species remained the same. Some aetosaurs ,

1860-508: Is likely a paraphyletic group rather than a true clade. Tanystropheids were a family of protorosaurs which elevated their neck size to extremes, with the largest genus Tanystropheus having a neck longer than its body. The protorosaur family Sharovipterygidae used their elongated hindlimbs for gliding. Other archosauromorphs, such as rhynchosaurs and allokotosaurs , were mostly stocky-bodied herbivores with specialized jaw structures. Rhynchosaurs, barrel-gutted herbivores, thrived for only

1953-465: Is no evidence of glaciation at or near either pole; in fact, the polar regions were apparently moist and temperate , providing a climate suitable for forests and vertebrates, including reptiles. Pangaea's large size limited the moderating effect of the global ocean; its continental climate was highly seasonal, with very hot summers and cold winters. The strong contrast between the Pangea supercontinent and

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2046-583: Is one of the two primary "daughter" clades of the Archosauria . The skull is often massively built, especially in contrast to ornithodires ; the snout is narrow and tends to be elongated, the neck is short and strong, and the limb posture ranges from a typical reptilian sprawl to an erect stance like dinosaurs ' or mammals ', although achieving it a different way. The body is often protected by two or more rows of armored plates. Many crurotarsans reached lengths of three meters or more. Pseudosuchians appeared during

2139-460: Is superimposed by 22 sea level drop events widespread in the geologic record, mostly of minor (less than 25-metre (82 ft)) and medium (25–75-metre (82–246 ft)) magnitudes. A lack of evidence for Triassic continental ice sheets suggest that glacial eustasy is unlikely to be the cause of these changes. The Triassic continental interior climate was generally hot and dry, so that typical deposits are red bed sandstones and evaporites . There

2232-459: Is usually divided into Early , Middle , and Late Triassic Epochs , and the corresponding rocks are referred to as Lower, Middle, or Upper Triassic. The faunal stages from the youngest to oldest are: During the Triassic, almost all the Earth's land mass was concentrated into a single supercontinent , Pangaea ( lit.   ' entire land ' ). This supercontinent was more-or-less centered on

2325-566: The Carnian (early part of the Late Triassic), some advanced cynodonts gave rise to the first mammals . During the Triassic, archosaurs displaced therapsids as the largest and most ecologically prolific terrestrial amniotes. This "Triassic Takeover" may have contributed to the evolution of mammals by forcing the surviving therapsids and their mammaliaform successors to live as small, mainly nocturnal insectivores . Nocturnal life may have forced

2418-545: The Jurassic , when the temnospondyls had become very rare. Most of the Reptiliomorpha , stem-amniotes that gave rise to the amniotes, disappeared in the Triassic, but two water-dwelling groups survived: Embolomeri that only survived into the early part of the period, and the Chroniosuchia , which survived until the end of the Triassic. The Permian–Triassic extinction devastated terrestrial life. Biodiversity rebounded as

2511-555: The Lake Lugano region of northern Italy and southern Switzerland , was in Middle Triassic times a lagoon behind reefs with an anoxic bottom layer, so there were no scavengers and little turbulence to disturb fossilization, a situation that can be compared to the better-known Jurassic Solnhofen Limestone lagerstätte . The remains of fish and various marine reptiles (including the common pachypleurosaur Neusticosaurus , and

2604-637: The Newark Supergroup . Rift basins are also common in South America, Europe, and Africa. Terrestrial environments are particularly well-represented in the South Africa, Russia, central Europe, and the southwest United States. Terrestrial Triassic biostratigraphy is mostly based on terrestrial and freshwater tetrapods, as well as conchostracans ("clam shrimps"), a type of fast-breeding crustacean which lived in lakes and hypersaline environments. Because

2697-469: The Olenekian and Anisian of Gondwana . Both kannemeyeriiform dicynodonts and gomphodont cynodonts remained important herbivores during much of the period. Therocephalians included both large predators ( Moschorhinus ) and herbivorous forms ( bauriids ) until their extinction midway through the period. Ecteniniid cynodonts played a role as large-sized, cursorial predators in the Late Triassic. During

2790-416: The pterosaurs . Therapsids , the dominant vertebrates of the preceding Permian period, saw a brief surge in diversification in the Triassic, with dicynodonts and cynodonts quickly becoming dominant, but they declined throughout the period with the majority becoming extinct by the end. However, the first stem-group mammals ( mammaliamorphs ), themselves a specialized subgroup of cynodonts, appeared during

2883-713: The surviving species repopulated empty terrain, but these were short-lived. Diverse communities with complex food-web structures took 30 million years to reestablish. Archosauromorph reptiles, which had already appeared and diversified to an extent in the Permian Period, exploded in diversity as an adaptive radiation in response to the Permian-Triassic mass extinction. By the Early Triassic, several major archosauromorph groups had appeared. Long-necked, lizard-like early archosauromorphs were known as protorosaurs , which

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2976-514: The thecodonts ) disappeared, as did most of the large labyrinthodont amphibians, groups of small reptiles, and most synapsids. Some of the early, primitive dinosaurs also became extinct, but more adaptive ones survived to evolve into the Jurassic. Surviving plants that went on to dominate the Mesozoic world included modern conifers and cycadeoids. The cause of the Late Triassic extinction is uncertain. It

3069-437: The traversodont cynodonts—were much reduced in the northern half of Pangaea ( Laurasia ). These extinctions within the Triassic and at its end allowed the dinosaurs to expand into many niches that had become unoccupied. Dinosaurs became increasingly dominant, abundant and diverse, and remained that way for the next 150 million years. The true "Age of Dinosaurs" is during the following Jurassic and Cretaceous periods, rather than

3162-791: The Anisian to Ladinian of the Tethysian domain, and from the Carnian and Rhaetian of a larger area that includes also the Boreal domain (e.g., Svalbard Islands), the North American continent, the South China block and Argentina . The best-studied of such episodes of humid climate, and probably the most intense and widespread, was the Carnian Pluvial Event . The Early Triassic was the hottest portion of

3255-405: The Carnian and include early sauropodomorphs and theropods. Most Triassic dinosaurs were small predators and only a few were common, such as Coelophysis , which was 1 to 2 metres (3.3 to 6.6 ft) long. Triassic sauropodomorphs primarily inhabited cooler regions of the world. The large predator Smok was most likely also an archosaur, but it is uncertain if it was a primitive dinosaur or

3348-552: The Early Triassic, forming small patches of reefs of modest extent compared to the great reef systems of Devonian or modern times. At the end of the Carnian, a reef crisis occurred in South China. Serpulids appeared in the Middle Triassic. Microconchids were abundant. The shelled cephalopods called ammonites recovered, diversifying from a single line that survived the Permian extinction. Bivalves began to rapidly diversify during

3441-402: The Early Triassic, while others (e.g. capitosaurs ) remained successful throughout the whole period, or only came to prominence in the Late Triassic (e.g. Plagiosaurus , metoposaurs ). The first Lissamphibians (modern amphibians) appear in the Triassic, with the progenitors of the first frogs already present by the Early Triassic. However, the group as a whole did not become common until

3534-549: The Early and Middle Triassic. Sea level rise accelerated in the Ladinian, culminating with a sea level up to 50 metres (164 ft) above present-day levels during the Carnian. Sea level began to decline in the Norian, reaching a low of 50 metres (164 ft) below present sea level during the mid-Rhaetian. Low global sea levels persisted into the earliest Jurassic. The long-term sea level trend

3627-403: The Jurassic. The Triassic was named in 1834 by Friedrich August von Alberti , after a succession of three distinct rock layers (Greek triás meaning 'triad') that are widespread in southern Germany : the lower Buntsandstein (colourful sandstone ) , the middle Muschelkalk (shell-bearing limestone ) and the upper Keuper (coloured clay ). On the geologic time scale , the Triassic

3720-602: The Jurassic. There were many types of marine reptiles. These included the Sauropterygia , which featured pachypleurosaurus and nothosaurs (both common during the Middle Triassic, especially in the Tethys region), placodonts , the earliest known herbivorous marine reptile Atopodentatus , and the first plesiosaurs . The first of the lizardlike Thalattosauria ( askeptosaurs ) and the highly successful ichthyopterygians , which appeared in Early Triassic seas, soon diversified. By

3813-580: The Latest Olenekian Cooling (LOC), from 248 to 247 Ma, temperatures cooled by about 6 °C. The Middle Triassic was cooler than the Early Triassic, with temperatures falling over most of the Anisian, with the exception of a warming spike in the latter portion of the stage. From 242 to 233 Ma, the Ladinian-Carnian Cooling (LCC) ensued. At the beginning of the Carnian, global temperatures continued to be relatively cool. The eruption of

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3906-478: The Middle Triassic, becoming highly abundant in the oceans. Aquatic insects rapidly diversified during the Middle Triassic, with this time interval representing a crucial diversification for Holometabola , the clade containing the majority of modern insect species. In the wake of the Permian-Triassic mass extinction event , the fish fauna was remarkably uniform, with many families and genera exhibiting

3999-597: The Middle Triassic, some ichthyopterygians were achieving very large body masses. Among other reptiles, the earliest turtles , like Proganochelys and Proterochersis , appeared during the Norian Age (Stage) of the Late Triassic Period. The Lepidosauromorpha , specifically the Sphenodontia , are first found in the fossil record of the earlier Carnian Age, though the earliest lepidosauromorphs likely occurred in

4092-450: The Permian extinction, Archaeplastida (red and green algae) had been the major marine phytoplanktons since about 659–645 million years ago, when they replaced marine planktonic cyanobacteria , which first appeared about 800 million years ago, as the dominant phytoplankton in the oceans. In the Triassic, secondary endosymbiotic algae became the most important plankton. In marine environments , new modern types of corals appeared in

4185-470: The Permian. The Procolophonidae , the last surviving parareptiles , were an important group of small lizard-like herbivores. The drepanosaurs were a clade of unusual, chameleon-like arboreal reptiles with birdlike heads and specialised claws. Three therapsid groups survived into the Triassic: dicynodonts , therocephalians , and cynodonts . The cynodont Cynognathus was a characteristic top predator in

4278-408: The Triassic (teleosts are by far the most diverse group of fish today). Predatory actinopterygians such as saurichthyids and birgeriids , some of which grew over 1.2 m (3.9 ft) in length, appeared in the Early Triassic and became widespread and successful during the period as a whole. Lakes and rivers were populated by lungfish (Dipnoi), such as Ceratodus , which are mainly known from

4371-497: The Triassic and survived the extinction event. The earliest known neopterygian fish, including early holosteans and teleosts , appeared near the beginning of the Triassic, and quickly diversified to become among the dominant groups of fish in both freshwater and marine habitats. The vast supercontinent of Pangaea dominated the globe during the Triassic, but in the latest Triassic ( Rhaetian ) and Early Jurassic it began to gradually rift into two separate landmasses: Laurasia to

4464-458: The Triassic and would survive the extinction event, allowing them to radiate during the Jurassic. Amphibians were primarily represented by the temnospondyls , giant aquatic predators that had survived the end-Permian extinction and saw a new burst of diversification in the Triassic, before going extinct by the end; however, early crown-group lissamphibians (including stem-group frogs , salamanders and caecilians ) also became more common during

4557-468: The Triassic, and may have first occurred in the Early Triassic if some archosaurian taxa such as Scythosuchus and Tsylmosuchus are considered to be within the family. An early cladistic analysis of crocodylotarsan ( pseudosuchian ) archosaurs included Lotosaurus , Fasolasuchus , Rauisuchus , and "the Kupferzell rauisuchid" (later called Batrachotomus ) within the Rauisuchidae. However,

4650-588: The Triassic, enlarging the Neo-Tethys Ocean which formed in their wake. At the same time, they forced the Paleo-Tethys Ocean to shrink as it was being subducted under Asia. By the end of the Triassic, the Paleo-Tethys Ocean occupied a small area and the Cimmerian terranes began to collide with southern Asia. This collision, known as the Cimmerian Orogeny , continued into the Jurassic and Cretaceous to produce

4743-487: The Triassic. Pseudosuchia Pseudosuchia (from Greek : ψεύδος (pseudos) , "false" and Greek : σούχος (souchos) , "crocodile") is one of two major divisions of Archosauria , including living crocodilians and all archosaurs more closely related to crocodilians than to birds. Pseudosuchians are also informally known as "crocodilian-line archosaurs", in contrast to the "bird-line archosaurs" or Avemetatarsalia . Despite Pseudosuchia meaning "false crocodiles",

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4836-796: The Wrangellia Large Igneous Province around 234 Ma caused abrupt global warming, terminating the cooling trend of the LCC. This warming was responsible for the Carnian Pluvial Event and resulted in an episode of widespread global humidity. The CPE ushered in the Mid-Carnian Warm Interval (MCWI), which lasted from 234 to 227 Ma. At the Carnian-Norian boundary occurred a positive δ C excursion believed to signify an increase in organic carbon burial. From 227 to 217 Ma, there

4929-521: The birds, while the crocodilians continued with little change. Today, the crocodiles , alligators , and gharials are the surviving representatives of this lineage. The Mesozoic range of cranial disparity is higher than the Triassic one, suggesting crocodylomorphs attained a high degree of diversification compared to Triassic pseudosuchians. Pseudosuchia was defined as a stem-based clade in 1985. It includes crocodiles and all archosaurs more closely related to crocodiles than to birds. A second clade with

5022-450: The bizarre long-necked archosauromorph Tanystropheus ), along with some terrestrial forms like Ticinosuchus and Macrocnemus , have been recovered from this locality. All these fossils date from the Anisian and Ladinian ages (about 242 Ma ago). The Triassic Period ended with a mass extinction, which was particularly severe in the oceans; the conodonts disappeared, as did all

5115-427: The chief terrestrial vertebrates during this time. A specialized group of archosaurs, called dinosaurs , first appeared in the Late Triassic but did not become dominant until the succeeding Jurassic Period. Archosaurs that became dominant in this period were primarily pseudosuchians , relatives and ancestors of modern crocodilians , while some archosaurs specialized in flight, the first time among vertebrates, becoming

5208-506: The dental plates, abundant in the fossils record. Hybodonts , a group of shark-like cartilaginous fish , were dominant in both freshwater and marine environments throughout the Triassic. Last survivors of the mainly Palaeozoic Eugeneodontida are known from the Early Triassic. Temnospondyl amphibians were among those groups that survived the Permian–Triassic extinction. Once abundant in both terrestrial and aquatic environments,

5301-428: The dominant carnivores in the early Triassic. Phytosaurs were a particularly common group which prospered during the Late Triassic. These long-snouted and semiaquatic predators resemble living crocodiles and probably had a similar lifestyle, hunting for fish and small reptiles around the water's edge. However, this resemblance is only superficial and is a prime-case of convergent evolution. True archosaurs appeared in

5394-504: The dominant terrestrial carnivores and herbivores. As the Mesozoic progressed, the Protosuchia gave rise to more typically crocodile-like forms. While dinosaurs were the dominant animals on land, the crocodiles flourished in rivers, swamps, and the oceans, with far greater diversity than they have today. With the end-Cretaceous extinction , the dinosaurs became extinct, with the exception of

5487-405: The early Triassic, splitting into two branches: Avemetatarsalia (the ancestors to birds) and Pseudosuchia (the ancestors to crocodilians). Avemetatarsalians were a minor component of their ecosystems, but eventually produced the earliest pterosaurs and dinosaurs in the Late Triassic. Early long-tailed pterosaurs appeared in the Norian and quickly spread worldwide. Triassic dinosaurs evolved in

5580-607: The entire Phanerozoic, seeing as it occurred during and immediately after the discharge of titanic volumes of greenhouse gases from the Siberian Traps. The Early Triassic began with the Permian-Triassic Thermal Maximum (PTTM) and was followed by the brief Dienerian Cooling (DC) from 251 to 249 Ma, which was in turn followed by the Latest Smithian Thermal Maximum (LSTT) around 249 to 248 Ma. During

5673-467: The equator and extended between the poles, though it did drift northwards as the period progressed. Southern Pangea, also known as Gondwana , was made up by closely-appressed cratons corresponding to modern South America , Africa , Madagascar , India , Antarctica , and Australia . North Pangea, also known as Laurussia or Laurasia , corresponds to modern-day North America and the fragmented predecessors of Eurasia . The western edge of Pangea lay at

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5766-531: The extinct family Cheirolepidiaceae , which first appeared in the Late Triassic, and would be prominent throughout most of the rest of the Mesozoic. No known coal deposits date from the start of the Triassic Period. This is known as the Early Triassic "coal gap" and can be seen as part of the Permian–Triassic extinction event . Possible explanations for the coal gap include sharp drops in sea level at

5859-424: The extinction of all the pseudosuchians with the exception of Sphenosuchia and Crocodyliformes (both Crocodylomorpha ), the latter being the ancestors of modern-day crocodiles. A study published in 2010 postulates that there is significant evidence that volcanic eruptions changed the climate, causing a mass extinction that wiped out the dinosaurs' main competitors. This allowed the dinosaurs to succeed them as

5952-744: The first to establish the name Pseudosuchia in a phylogenetic context, using it as a branch-based taxon for all archosaurs more closely related to crocodilians than to birds. This made the name Pseudosuchia somewhat ironic because true crocodiles (i.e. members of Crocodylia) were now included in the group. Phylogenetic definitions of Pseudosuchia include "Crocodiles and all archosaurs closer to crocodiles than to birds" (Gauthier and Padian), "Extant crocodiles and all extinct archosaurs that are closer to crocodiles than they are to birds" (Gauthier, 1986), and more recently "the most inclusive clade within Archosauria that includes Crocodylia but not Aves" (Senter, 2005). As

6045-510: The global ocean triggered intense cross-equatorial monsoons , sometimes referred to as the Pangean megamonsoons . The Triassic may have mostly been a dry period, but evidence exists that it was punctuated by several episodes of increased rainfall in tropical and subtropical latitudes of the Tethys Sea and its surrounding land. Sediments and fossils suggestive of a more humid climate are known from

6138-490: The heavily armored aetosaurs , and several were bipedal, such as Poposaurus and Postosuchus . The bizarre, ornithomimid -like shuvosaurids were both bipedal and herbivorous, with toothless beaks. Many of these Triassic pseudosuchian groups went extinct at or before the Triassic–Jurassic extinction event . However, one group, the crocodylomorphs , survived the major extinction. Crocodylomorphs themselves evolved

6231-420: The impact. So, the evidence suggests the Manicouagan impact preceded the end of the Triassic by approximately 10±2 Ma. It could not therefore be the immediate cause of the observed mass extinction. The number of Late Triassic extinctions is disputed. Some studies suggest that there are at least two periods of extinction towards the end of the Triassic, separated by 12 to 17 million years. But arguing against this

6324-401: The keystone predators of most Triassic terrestrial ecosystems. Over 25 species have been found, including giant quadrupedal hunters, sleek bipedal omnivores, and lumbering beasts with deep sails on their backs. They probably occupied the large-predator niche later filled by theropods. "Rauisuchians" were ancestral to small, lightly-built crocodylomorphs, the only pseudosuchians which survived into

6417-472: The late Olenekian (early Triassic ); by the Ladinian (late Middle Triassic) they dominated the terrestrial carnivore niches. Their heyday was the Late Triassic, during which time their ranks included erect-limbed rauisuchians , herbivorous armored aetosaurs , the large predatory poposaurs , the small agile sphenosuchian crocodilians, and a few other assorted groups. The end-Triassic extinction caused

6510-399: The late 20th century, especially after the name Crurotarsi was established in 1990 to label the clade (evolutionary grouping) of archosaurs encompassing most reptiles previously identified as pseudosuchians. By this time, Pseudosuchia had also been defined as a clade , but it was not widely embraced until 2011. In 2011 paleontologist Sterling Nesbitt proposed that Crurotarsi, as it

6603-412: The latter clade encompasses all crocodilian-line archosaurs in most phylogenetic analyses. Sterling Nesbitt 's 2011 analysis places one crurotarsan group, Phytosauria, outside Pseudosuchia. Since the definition of Crurotarsi relies on phytosaurs, their placement outside Pseudosuchia (and thus Archosauria) means that the clade Crurotarsi includes both pseudosuchians and avemetatarsalians. Pseudosuchia

6696-540: The mammaliaforms to develop fur and a higher metabolic rate . Two Early Triassic lagerstätten (high-quality fossil beds), the Dienerian aged Guiyang biota and the earliest Spathian aged Paris biota stand out due to their exceptional preservation and diversity . They represent the earliest lagerstätten of the Mesozoic era and provide insight into the biotic recovery from the Permian-Triassic mass extinction event. The Monte San Giorgio lagerstätte, now in

6789-573: The margin of an enormous ocean, Panthalassa ( lit.   ' entire sea ' ), which roughly corresponds to the modern Pacific Ocean . Practically all deep-ocean crust present during the Triassic has been recycled through the subduction of oceanic plates, so very little is known about the open ocean from this time period. Most information on Panthalassan geology and marine life is derived from island arcs and rare seafloor sediments accreted onto surrounding land masses, such as present-day Japan and western North America. The eastern edge of Pangea

6882-453: The marine reptiles except ichthyosaurs and plesiosaurs . Invertebrates like brachiopods and molluscs (such as gastropods ) were severely affected. In the oceans, 22% of marine families and possibly about half of marine genera went missing. Though the end-Triassic extinction event was not equally devastating in all terrestrial ecosystems, several important clades of crurotarsans (large archosaurian reptiles previously grouped together as

6975-517: The most inclusive clade containing Rauisuchus tiradentes , but not Prestosuchus chiniquensis , Poposaurus gracilis , or Crocodylus niloticus (the Nile crocodile). In this modern sense, rauisuchids are recovered as members of the clade Loricata , being the sister taxon of Crocodylomorpha (the group including living crocodilians ), and being more derived than taxa such as Prestosuchus and Batrachotomus . Rauisuchids occurred throughout much of

7068-512: The name "false crocodiles". In mid-20th century textbooks, like Alfred Sherwood Romer 's Vertebrate Paleontology and Edwin H. Colbert 's Evolution of the Vertebrates , Pseudosuchia constitutes one of the suborders of the now-abandoned order Thecodontia . Zittel's aetosaurs were placed in their own suborder, Aetosauria. Colbert considered small lightly built archosaurs, such as Ornithosuchus and Hesperosuchus — both of which were at

7161-470: The name is a misnomer as true crocodilians are now defined as a subset of the group. The clade Pseudosuchia is potentially equivalent to Crurotarsi even though the latter has a different, node-based definition: "all taxa the least inclusive clade containing Rutiodon carolinensis (Emmons, 1856), and Crocodylus niloticus (Laurenti, 1768)." However, a major 2011 study of Triassic archosaur relations proposed that Rutiodon 's group, Phytosauria ,

7254-430: The next most common tetrapods, and early dinosaurs, passed through unchanged. However, both phytosaurs and aetosaurs were among the groups of archosaur reptiles completely wiped out by the end-Triassic extinction event. It seems likely then that there was some sort of end-Carnian extinction, when several herbivorous archosauromorph groups died out, while the large herbivorous therapsids —the kannemeyeriid dicynodonts and

7347-453: The north and Gondwana to the south. The global climate during the Triassic was mostly hot and dry, with deserts spanning much of Pangaea's interior. However, the climate shifted and became more humid as Pangaea began to drift apart. The end of the period was marked by yet another major mass extinction, the Triassic–Jurassic extinction event , that wiped out many groups, including most pseudosuchians, and allowed dinosaurs to assume dominance in

7440-402: The order Isoetales (which contains living quillworts ), rose to prominence due to the environmental instability following the Permian-Triassic extinction, with one particularly notable example being the genus Pleuromeia , which grew in columnar like fashion, sometimes reaching a height of 2 metres (6.6 ft). The relevance of lycophytes declined from the Middle Triassic onwards, following

7533-478: The return of more stable environmental conditions. While having first appeared during the Permian, the extinct seed plant group Bennettitales first became a prominent element in global floras during the Late Triassic, a position they would hold for much of the Mesozoic. In the Southern Hemisphere landmasses of Gondwana, the tree Dicroidium , an extinct " seed fern " belong to the order Corystospermales

7626-408: The sister taxon of Archosauria, and therefore not crocodile-line archosaurs. Because phytosaurs are included in the definition of Crurotarsi, crurotarsans are not solely crocodile-line archosaurs, but also bird-line archosaurs and phytosaurs. Under this phylogeny, Crurotarsi includes phytosaurs, crocodiles, pterosaurs, and dinosaurs, while Pseudosuchia still contains only crocodile-line archosaurs. Below

7719-647: The terminus of the Triassic, there was an extreme warming event referred to as the End-Triassic Thermal Event (ETTE), which was responsible for the Triassic-Jurassic mass extinction. Bubbles of carbon dioxide in basaltic rocks dating back to the end of the Triassic indicate that volcanic activity from the Central Atlantic Magmatic Province helped trigger climate change in the ETTE. During the Early Triassic, lycophytes , particularly those of

7812-587: The terrestrial species had mostly died out during the extinction event. The Triassic survivors were aquatic or semi-aquatic, and were represented by Tupilakosaurus , Thabanchuia , Branchiosauridae and Micropholis , all of which died out in Early Triassic, and the successful Stereospondyli , with survivors into the Cretaceous Period. The largest Triassic stereospondyls, such as Mastodonsaurus , were up to 4 to 6 metres (13 to 20 ft) in length. Some lineages (e.g. trematosaurs ) flourished briefly in

7905-570: The time of the Permo-Triassic boundary; acid rain from the Siberian Traps eruptions or from an impact event that overwhelmed acidic swamps; climate shift to a greenhouse climate that was too hot and dry for peat accumulation; evolution of fungi or herbivores that were more destructive of wetlands; the extinction of all plants adapted to peat swamps, with a hiatus of several million years before new plant species evolved that were adapted to peat swamps; or soil anoxia as oxygen levels plummeted. Before

7998-523: The time reconstructed as theropod dinosaur-like bipeds — to be typical pseudosuchians. These small forms were assumed to be the ancestors of all later archosaurs. The name Pseudosuchia became a wastebasket taxon into which all thecodonts that did not fit in the other three suborders could be placed. Even Sharovipteryx and Longisquama , two enigmatic Triassic reptiles that bear little resemblance to archosaurs, have been regarded as pseudosuchians. Gauthier and Padian (1985) and Gauthier (1986) became

8091-500: The wake of the Permian–Triassic extinction event , which left the Earth's biosphere impoverished; it was well into the middle of the Triassic before life recovered its former diversity. Three categories of organisms can be distinguished in the Triassic record: survivors from the extinction event, new groups that flourished briefly, and other new groups that went on to dominate the Mesozoic Era. Reptiles , especially archosaurs , were

8184-594: Was a dominant element in forest habitats across the region during the Middle-Late Triassic. During the Late Triassic, the Ginkgoales (which today are represented by only a single species, Ginkgo biloba ) underwent considerable diversification. Conifers were abundant during the Triassic, and included the Voltziales (which contains various lineages, probably including those ancestral to modern conifers), as well as

8277-646: Was a relatively cool period known as the Early Norian Cool Interval (ENCI), after which occurred the Mid-Norian Warm Interval (MNWI) from 217 to 209 Ma. The MNWI was briefly interrupted around 214 Ma by a cooling possibly related to the Manicouagan impact . Around 212 Ma, a 10 Myr eccentricity maximum caused a paludification of Pangaea and a reduction in the size of arid climatic zones. The Rhaetian Cool Interval (RCI) lasted from 209 to 201 Ma. At

8370-491: Was accompanied by huge volcanic eruptions that occurred as the supercontinent Pangaea began to break apart about 202 to 191 million years ago (40Ar/39Ar dates), forming the Central Atlantic Magmatic Province (CAMP), one of the largest known inland volcanic events since the planet had first cooled and stabilized. Other possible but less likely causes for the extinction events include global cooling or even

8463-479: Was encroached upon by a pair of extensive oceanic basins: The Neo-Tethys (or simply Tethys) and Paleo-Tethys Oceans . These extended from China to Iberia, hosting abundant marine life along their shallow tropical peripheries. They were divided from each other by a long string of microcontinents known as the Cimmerian terranes . Cimmerian crust had detached from Gondwana in the early Permian and drifted northwards during

8556-404: Was not closely related to other traditional "crurotarsans", at least compared to avemetatarsalians such as pterosaurs and dinosaurs . As a result, Crurotarsi could be a much broader clade than Pseudosuchia. Other recent studies support a more traditional phylogeny. Contrary to popular belief, crocodilians differ significantly from their ancestors and distant relatives, as Pseudosuchia contains

8649-568: Was then defined, must include not only crocodilian-line archosaurs, but all other archosaurs including birds, non-avian dinosaurs , and pterosaurs . The clade Pseudosuchia as originally defined could still be used to identify crocodilian-line archosaurs, and since many recent studies support Nesbitt's findings, Pseudosuchia is again commonly used. The name Pseudosuchia was coined by Karl Alfred von Zittel in 1887–1890 to include three taxa (two aetosaurs and Dyoplax ) that were superficially crocodilian-like, but were not actually crocodilian. Hence

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