Late Triassic in the context of "Chinle Formation"

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👉 Late Triassic in the context of Chinle Formation

The Chinle Formation is an Upper Triassic continental geological formation of fluvial, lacustrine, and palustrine to eolian deposits spread across the U.S. states of Nevada, Utah, northern Arizona, western New Mexico, and western Colorado. In New Mexico, it is often raised to the status of a geological group, the Chinle Group. Some authors have controversially considered the Chinle to be synonymous to the Dockum Group of eastern Colorado and New Mexico, western Texas, the Oklahoma panhandle, and southwestern Kansas. The Chinle Formation is part of the Colorado Plateau, Basin and Range, and the southern section of the Interior Plains. A probable separate depositional basin within the Chinle is found in northwestern Colorado and northeastern Utah. The southern portion of the Chinle reaches a maximum thickness of a little over 520 meters (1,710 ft). Typically, the Chinle rests unconformably on the Moenkopi Formation.

The Chinle Formation was probably mostly deposited in the Norian stage, according to a plethora of chronological techniques. It is a thick and fossiliferous formation with numerous named members (subunits) throughout its area of deposition.

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Late Triassic in the context of Triassic

The Triassic (/trˈæsɪk/; sometimes symbolized as 🝈) is a geologic period and a stratigraphic system that spans 50.5 million years from the end of the Permian Period 251.902 Ma (million years ago) to the beginning of the Jurassic Period 201.4 Ma. The Triassic Period is the first and shortest geologic period of the Mesozoic Era, and the seventh period of the Phanerozoic Eon. The start and the end of the Triassic Period featured major extinction events.

Chronologically, the Triassic Period is divided into three epochs: (i) the Early Triassic, (ii) the Middle Triassic, and (iii) the Late Triassic. The Triassic Period began after the Permian–Triassic extinction event that much reduced the biosphere of planet Earth. The fossil record of the Triassic Period presents three categories of organisms: (i) animals that survived the Permian–Triassic extinction event, (ii) new animals that briefly flourished in the Triassic biosphere, and (iii) new animals that evolved and dominated the Mesozoic Era. Reptiles, especially archosaurs, were 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 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 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 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.

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Late Triassic in the context of Theropod

Theropoda (/θɪəˈrɒpədə/; from ancient Greek θηρίο- ποδός [θηρίον, (therion) "wild beast"; πούς, ποδός (pous, podos) "foot"]) is one of the three major clades of dinosaur, alongside Ornithischia and Sauropodomorpha. Theropods, both extant and extinct, are characterized by hollow bones and three toes and claws on each limb. They are generally classed as a group of saurischian dinosaurs, placing them closer to sauropodomorphs than to ornithischians. They were ancestrally carnivorous, although a number of theropod groups evolved to become herbivores and omnivores. Members of the subgroup Coelurosauria were most likely all covered with feathers, and it is possible that they were also present in other theropods. In the Jurassic, birds evolved from small specialized coelurosaurian theropods, and are currently represented by about 11,000 living species, making theropods the only group of dinosaurs alive today.

Theropods first appeared during the Carnian age of the Late Triassic period 231.4 million years ago (Ma) and included the majority of large terrestrial carnivores from the Early Jurassic until the end of the Cretaceous, about 66 Ma, including the largest terrestrial carnivorous animals ever, such as Tyrannosaurus and Giganotosaurus, though non-avian theropods exhibited considerable size diversity, with some non-avian theropods like scansoriopterygids being no bigger than small birds.

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Late Triassic in the context of Pterosaur

Pterosaurs are an extinct clade of flying reptiles in the order Pterosauria. They existed during most of the Mesozoic: from the Late Triassic to the end of the Cretaceous (228 million to 66 million years ago). Pterosaurs are the earliest vertebrates known to have evolved powered flight. Their wings were formed by a membrane of skin, muscle, and other tissues stretching from the ankles to a dramatically lengthened fourth finger.

Traditionally, pterosaurs were divided into two major types. Basal pterosaurs (also called non-pterodactyloid pterosaurs or 'rhamphorhynchoids') were smaller animals, up to two meter wingspan, with fully toothed jaws and, typically, long tails. Their wide wing membranes probably included and connected the hindlimbs. On the ground, they would have had an awkward sprawling posture due to short metacarpals, but the anatomy of their joints and strong claws would have made them effective climbers, and some may have lived in trees. Basal pterosaurs were insectivores, piscivores or predators of small land vertebrates. Later pterosaurs (pterodactyloids) evolved many sizes, shapes, and lifestyles. Pterodactyloids had narrower wings with free hindlimbs, highly reduced tails, and long necks with large heads. On the ground, they walked well on all four limbs due to long metacarpals with an upright posture, standing plantigrade on the hind feet and folding the wing finger upward to walk on the metacarpals with the three smaller fingers of the hand pointing to the rear. They could take off from the ground, and fossil trackways show that at least some species were able to run, wade, and/or swim. Their jaws had horny beaks, and some groups lacked teeth. Some groups developed elaborate head crests with sexual dimorphism. Since 2010 it is understood that many species, the basal Monofenestrata, were intermediate in build, combining an advanced long skull with long tails.

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Late Triassic in the context of Petrified wood

Petrified wood (from Ancient Greek πέτρα meaning 'rock' or 'stone'; literally 'wood turned into stone'), is the name given to a special type of fossilized wood, the fossilized remains of terrestrial vegetation. Petrifaction is the result of a tree or tree-like plants having been replaced by stone via a mineralization process that often includes permineralization and replacement. The organic materials making up cell walls have been replicated with minerals (mostly silica in the form of opal, chalcedony, or quartz). In some instances, the original structure of the stem tissue may be partially retained. Unlike other plant fossils, which are typically impressions or compressions, petrified wood is a three-dimensional representation of the original organic material.

The petrifaction process occurs underground, when wood becomes buried in water or volcanic ash. The presence of water reduces the availability of oxygen which inhibits aerobic decomposition by bacteria and fungi. Mineral-laden water flowing through the sediments may lead to permineralization, which occurs when minerals precipitate out of solution filling the interiors of cells and other empty spaces. During replacement, the plant's cell walls act as a template for mineralization. There needs to be a balance between the decay of cellulose and lignin and mineral templating for cellular detail to be preserved with fidelity. Most of the organic matter often decomposes, however some of the lignin may remain. Silica in the form of opal-A, can encrust and permeate wood relatively quickly in hot spring environments. However, petrified wood is most commonly associated with trees that were buried in fine grained sediments of deltas and floodplains or volcanic lahars and ash beds. A forest where such material has petrified becomes known as a petrified forest.

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Late Triassic in the context of Glen Canyon Group

The Glen Canyon Group is a geologic group of formations that is spread across the U.S. states of Nevada, Utah, northern Arizona, north west New Mexico and western Colorado. It is called the Glen Canyon Sandstone in the Green River Basin of Colorado and Utah.

There are four formations within the group. From oldest to youngest, these are the Wingate Sandstone, Moenave Formation, Kayenta Formation, and Navajo Sandstone. Part of the Colorado Plateau and the Basin and Range, this group of formations was laid down during the Late Triassic and Early Jurassic, with the Triassic-Jurassic boundary within the Wingate Sandstone. The top of the Glen Canyon Group is thought to date to the Toarcian stage of the Early Jurassic.

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Late Triassic in the context of Sauropod

Sauropoda (/sɔːˈrɒpədə/), whose members are called sauropods (/ˈsɔːrəpɒdz/; from sauro- + -pod; lit.'lizard-footed'), is a clade of saurischian ('lizard-hipped') dinosaurs. Sauropods had very long necks, long tails, small heads (relative to the rest of their body), and four thick, pillar-like legs. They are notable for the enormous sizes attained by some species, and the group includes the largest animals to have ever lived on land. Well-known genera include Alamosaurus, Apatosaurus, Argentinosaurus, Brachiosaurus, Brontosaurus, Camarasaurus, Diplodocus, Dreadnoughtus, and Mamenchisaurus.

The oldest known unequivocal sauropod dinosaurs are known from the Early Jurassic. Isanosaurus and Antetonitrus were originally described as Triassic sauropods, but their age, and in the case of Antetonitrus also its sauropod status, were subsequently questioned. Sauropod-like sauropodomorph tracks from the Fleming Fjord Formation (Greenland) might, however, indicate the occurrence of the group in the Late Triassic. By the Late Jurassic (150 million years ago), sauropods had become widespread (especially the diplodocids and brachiosaurids). By the Late Cretaceous, one group of sauropods, the titanosaurs, had replaced all others and had a near-global distribution. However, as with all other non-avian dinosaurs alive at the time, the titanosaurs died out in the Cretaceous–Paleogene extinction event. Fossilised remains of sauropods have been found on every continent, including Antarctica.

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Late Triassic in the context of Middle Triassic

In the geologic timescale, the Middle Triassic is the second of three epochs of the Triassic period or the middle of three series in which the Triassic system is divided in chronostratigraphy. The Middle Triassic spans the time between 246.7 Ma and 237 Ma (million years ago). It is preceded by the Early Triassic Epoch and followed by the Late Triassic Epoch. The Middle Triassic is divided into the Anisian and Ladinian ages or stages.

Formerly the middle series in the Triassic was also known as Muschelkalk. This name is now only used for a specific unit of rock strata with approximately Middle Triassic age, found in western Europe.

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