Jurassic in the context of Tuatara


Jurassic in the context of Tuatara

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⭐ Core Definition: Jurassic

The Jurassic (/ʊˈræsɪk/ juurr-ASS-ik) is a geologic period and stratigraphic system that spanned from the end of the Triassic Period 201.4 Ma (million years ago) to the beginning of the Cretaceous Period, 143.1 Ma. The Jurassic constitutes the second and middle period of the Mesozoic Era as well as the eighth period of the Phanerozoic Eon and is named after the Jura Mountains, where limestone strata from the period were first identified.

The start of the Jurassic was marked by the major Triassic–Jurassic extinction event, associated with the eruption of the Central Atlantic Magmatic Province (CAMP). The beginning of the Toarcian Age started around 183 Ma and is marked by the Toarcian Oceanic Anoxic Event, a global episode of oceanic anoxia, ocean acidification, and elevated global temperatures associated with extinctions, likely caused by the eruption of the Karoo-Ferrar large igneous provinces. The end of the Jurassic, however, has no clear, definitive boundary with the Cretaceous and is the only boundary between geological periods to remain formally undefined.

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Jurassic in the context of Desiccation

Desiccation is the state of extreme dryness, or the process of extreme drying. A desiccant is a hygroscopic (attracts and holds water) substance that induces or sustains such a state in its local vicinity in a moderately sealed container. The word desiccation comes from Latin de- 'thoroughly' and siccare 'to dry'.

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Jurassic in the context of Izu–Bonin–Mariana Arc

The Izu–Bonin–Mariana (IBM) arc system is a tectonic plate convergent boundary in Micronesia. The IBM arc system extends over 2800 km south from Tokyo, Japan, to beyond Guam, and includes the Izu Islands, the Bonin Islands, and the Mariana Islands; much more of the IBM arc system is submerged below sealevel. The IBM arc system lies along the eastern margin of the Philippine Sea plate in the Western Pacific Ocean. It is the site of the deepest gash in Earth's solid surface, the Challenger Deep in the Mariana Trench.

The IBM arc system formed as a result of subduction of the western Pacific plate. The IBM arc system now subducts mid-Jurassic to Early Cretaceous lithosphere, with younger lithosphere in the north and older lithosphere in the south, including the oldest (~170 million years old, or Ma) oceanic crust. Subduction rates vary from ~2 cm (1 inch) per year in the south to 6 cm (~2.5 inches) in the north.

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Jurassic in the context of Madagascar

Madagascar, officially the Republic of Madagascar, is an island country in the Indian Ocean that includes the island of Madagascar and numerous smaller peripheral islands. Lying off the southeastern coast of Africa, it is the world's fourth-largest island, the second-largest island country, and the 46th-largest country overall. Its capital and largest city is Antananarivo.

Following the prehistoric breakup of the supercontinent Gondwana, Madagascar split from Africa during the Early Jurassic period, around 180 million years ago, and separated from the Indian subcontinent approximately 90 million years ago. This isolation allowed native plants and animals to evolve in relative seclusion; as a result, Madagascar is a biodiversity hotspot and one of the world's 17 megadiverse countries, with over 90% of its wildlife being endemic. The island has a subtropical to tropical maritime climate. Madagascar was first permanently settled during or before the mid-first millennium CE (roughly 500 to 700) by Austronesian peoples, presumably arriving on outrigger canoes from present-day Indonesia. These were joined around the ninth century by Bantu groups crossing the Mozambique Channel from East Africa. Other groups continued to settle on Madagascar over time, each one making lasting contributions to Malagasy cultural life. Consequently, there are 18 or more classified peoples of Madagascar, the most numerous being the Merina of the central highlands.

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Jurassic in the context of List of mountains in Albania

Albania is mostly mountainous, with the first alpine regions forming towards the end of the Jurassic period. During the Cenozoic era, the malformation of the Albanides accelerated, causing the subterranean landscape to take its present form. The average altitude of the country is 714 m (2,343 ft), almost three times that of Europe. Its highest summits are situated in the Albanian Alps and the eastern mountain range, with Korab being the highest peak, at 2,764 m (9,068 ft) above sea level.

The country's geography is unique due to its location and varied relief, with landscapes ranging from mediterranean in the west to a more continental influence in the east and mountainous terrain in the interior and east. This combination of plains, hills and mountains has resulted in a diverse range of geographical features, extending horizontally and vertically. However, this complexity has made regionalization challenging, as different authors have used alternating criteria and methods. In the 1920s, Herbert Louis proposed a scheme that divided Albania into two large regions: Inner Albania and Coastal Albania, each with specific subdivisions. His scheme was widely used until 1964, when it was to be replaced by Pandi Geço's proposed scheme which divided the country into four physiographic regions, listed as follows: Albanian Alps, Central Mountain Region, Southern Mountain Region, Albanian Coastal Lowlands and its hills. By 1990, Geço's scheme was improved through further research and consideration of ecological concerns, recapping all regions into 67 constituent subunits.

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Jurassic in the context of Skanderbeg Mountains

Skanderbeg Mountains (Albanian: Vargmalet e Skënderbeut), also known as Vargmalet Perëndimore, are a prominent mountain range situated in the northwestern section of the Central Mountain Region of Albania. The range stretches approximately 100 km (62 mi), making it the longest in the country. It extends from the Gjadër river valley in the northwest to the Shkumbin river valley in the southeast; and from the trough of Mat in the east, to the plains between Lezhë, Tirana and Lower Shkodër in the west.

The eastern side of the range is composed primarily of limestone from the Triassic-Jurassic periods, separated into distinct blocks, while the western side is composed of limestone from the Ordovician and the Cretaceous-Paleogene periods, forming belts amid the Paleogene flysch. Ultrabasic rocks are also present, and the older flysch appears in the form of surface bands on the eastern side of the range.

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Jurassic in the context of Moenave Formation

The Moenave Formation is a Mesozoic geologic formation, in the Glen Canyon Group. It is found in Utah and Arizona.

The Moenave was deposited on an erosion surface on the Chinle Formation following an early Jurassic uplift and unconformity that represents about ten million years of missing sedimentation. Periodic incursions of shallow seas from the north during the Jurassic flooded parts of Wyoming, Montana, and a northeast–southwest trending trough on the Utah/Idaho border. The Moenave was deposited in a variety of river, lake, and flood-plain environments, near the ancient Lake Dixie.

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Jurassic in the context of Flea

Flea, the common name for the order Siphonaptera, includes 2,500 species of small flightless insects that live as external parasites of mammals and birds. Fleas live by ingesting the blood of their hosts. Adult fleas grow to about 3 millimetres (18 inch) long, are usually dark in color, and have bodies that are "flattened" sideways or narrow, enabling them to move through their hosts' fur or feathers. They lack wings; their hind legs are extremely well adapted for jumping. Their claws keep them from being dislodged, and their mouthparts are adapted for piercing skin and sucking blood. Some species can leap 50 times their body length, a feat second only to jumps made by another group of insects, the superfamily of froghoppers. Flea larvae are worm-like, with no limbs; they have chewing mouthparts and feed on organic debris left on their hosts' skin.

Genetic evidence indicates that fleas are a specialised lineage of parasitic scorpionflies (Mecoptera) sensu lato, most closely related to the family Nannochoristidae. The earliest known fleas lived in the Middle Jurassic; modern-looking forms appeared in the Cenozoic. Fleas probably originated on mammals first and expanded their reach to birds. Each species of flea specializes, more or less, on one species of host: many species of flea never breed on any other host; some are less selective. Some families of fleas are exclusive to a single host group; for example, the Malacopsyllidae are found only on armadillos, the Ischnopsyllidae only on bats, and the Chimaeropsyllidae only on elephant shrews.

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Jurassic in the context of Dinosaur

Dinosaurs are a diverse group of reptiles of the clade Dinosauria. They first appeared during the Triassic period, between 243 and 233.23 million years ago (mya), although the exact origin and timing of the evolution of dinosaurs is a subject of active research. They became the dominant terrestrial vertebrates after the Triassic–Jurassic extinction event 201.3 mya and their dominance continued throughout the Jurassic and Cretaceous periods. The fossil record shows that birds are feathered dinosaurs, having evolved from earlier theropods during the Late Jurassic epoch, and are the only dinosaur lineage known to have survived the Cretaceous–Paleogene extinction event approximately 66 mya. Dinosaurs can therefore be divided into avian dinosaurs—birds—and the extinct non-avian dinosaurs, which are all dinosaurs other than birds.

Dinosaurs are varied from taxonomic, morphological and ecological standpoints. Birds, at over 11,000 living species, are among the most diverse groups of vertebrates. Using fossil evidence, paleontologists have identified over 900 distinct genera and more than 1,000 different species of non-avian dinosaurs. Dinosaurs are represented on every continent by both extant species (birds) and fossil remains. Through most of the 20th century, before birds were recognized as dinosaurs, most of the scientific community believed dinosaurs to have been sluggish and cold-blooded. Most research conducted since the 1970s, however, has indicated that dinosaurs were active animals with elevated metabolisms and numerous adaptations for social interaction. Some were herbivorous, others carnivorous. Evidence suggests that all dinosaurs were egg-laying, and that nest-building was a trait shared by many dinosaurs, both avian and non-avian.

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Jurassic in the context of Diplodocus

Diplodocus (/dɪˈplɒdəkəs/, /dˈplɒdəkəs/, or /ˌdɪplˈdkəs/) is an extinct genus of diplodocid sauropod dinosaurs known from the Late Jurassic of North America. The first fossils of Diplodocus were discovered in 1877 by S. W. Williston. The generic name, coined by Othniel Charles Marsh in 1878, is a Neo-Latin term derived from Greek διπλός (diplos) "double" and δοκός (dokos) "beam", in reference to the double-beamed chevron bones located in the underside of the tail, which were then considered unique.

The genus lived in what is now mid-western North America, at the end of the Jurassic period. It is one of the more common dinosaur fossils found in the middle to upper Morrison Formation, with most specimens being found in rocks dated between about 151.88 and 149.1 million years ago, during the latest Kimmeridgian Age, although it may have made it into the Tithonian, with at least one specimen (AMNH FR 223) being potentially from among the youngest deposits of the formation. The Morrison Formation records an environment and time dominated by gigantic sauropod dinosaurs, such as Apatosaurus, Barosaurus, Brachiosaurus, Brontosaurus, and Camarasaurus. Its great size may have been a deterrent to the predators Allosaurus and Ceratosaurus: their remains have been found in the same strata, which suggests that they coexisted with Diplodocus.

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Jurassic 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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Jurassic 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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Jurassic in the context of Clay mineral

Clay minerals are hydrous aluminium phyllosilicates (e.g. kaolin, Al2Si2O5(OH)4), sometimes with variable amounts of iron, magnesium, alkali metals, alkaline earths, and other cations found on or near some planetary surfaces.

Clay minerals form in the presence of water and have been important to life, and many theories of abiogenesis involve them. They are important constituents of soils, and have been useful to humans since ancient times in agriculture and manufacturing.

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Jurassic in the context of Araucaria

Araucaria ( /ærɔːˈkɛəriə/; original pronunciation: [a.ɾawˈka. ɾja]) is a genus of evergreen coniferous trees in the family Araucariaceae. While today they are largely confined to the Southern Hemisphere, during the Jurassic and Cretaceous they were globally distributed. There are 20 extant species in New Caledonia (where 14 species are endemic, see New Caledonian Araucaria), eastern Australia (including Norfolk Island), New Guinea, Argentina, Brazil, Chile and Uruguay.

The genus is familiar to many people as the genus of the distinctive Chilean pine or monkey-puzzle tree (Araucaria araucana). No distinct vernacular name exists for the genus. Many are called "pine", although they are only distantly related to true pines, in the genus Pinus.

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Jurassic in the context of Evolution of birds

The evolution of birds began in the Jurassic Period, with the earliest birds derived from a clade of theropod dinosaurs named Paraves. Birds are categorized as a biological class, Aves. For more than a century, the small theropod dinosaur Archaeopteryx lithographica from the Late Jurassic period was considered to have been the earliest bird. Modern phylogenies place birds in the dinosaur clade Theropoda. According to the current consensus, Aves and a sister group, the order Crocodilia, together are the sole living members of an unranked reptile clade, the Archosauria. Four distinct lineages of bird survived the Cretaceous–Paleogene extinction event 66 million years ago, giving rise to ostriches and relatives (Palaeognathae), waterfowl (Anseriformes), ground-living fowl (Galliformes), and "modern birds" (Neoaves).

Phylogenetically, Aves is usually defined as all descendants of the most recent common ancestor of a specific modern bird species (such as the house sparrow, Passer domesticus), and either Archaeopteryx, or some prehistoric species closer to Neornithes (to avoid the problems caused by the unclear relationships of Archaeopteryx to other theropods). If the latter classification is used then the larger group is termed Avialae. Currently, the relationship between non-avian dinosaurs, Archaeopteryx, and modern birds is still under debate.

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Jurassic in the context of Late Jurassic

The Late Jurassic is the third epoch of the Jurassic Period, and it spans the geologic time from 161.5 ± 1.0 to 143.1 ± 0.6 million years ago (Ma), which is preserved in Upper Jurassic strata.

In European lithostratigraphy, the name "Malm" indicates rocks of Late Jurassic age. In the past, Malm was also used to indicate the unit of geological time, but this usage is now discouraged to make a clear distinction between lithostratigraphic and geochronologic/chronostratigraphic units.

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Jurassic in the context of Termite

Termites are a group of detritophagous eusocial cockroaches which consume a variety of decaying plant material, generally in the form of wood, leaf litter, and soil humus. They are distinguished by their moniliform antennae and the soft-bodied, unpigmented worker caste for which they have been commonly termed "white ants"; however, they are not ants but highly derived cockroaches. About 2,997 extant species are currently described, 2,125 of which are members of the family Termitidae.

Termites comprise the infraorder Isoptera, or alternatively the epifamily Termitoidae, within the order Blattodea (the cockroaches). Termites were once classified in a separate order from cockroaches, but recent phylogenetic studies indicate that they evolved from cockroaches, as they are deeply nested within the group, and the sister group to wood-eating cockroaches of the genus Cryptocercus. Previous estimates suggested the divergence took place during the Jurassic or Triassic. More recent estimates suggest that they have an origin during the Late Jurassic, with the first fossil records in the Early Cretaceous.

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Jurassic in the context of Central American Seaway

The Central American Seaway (also known as the Panamanic Seaway, Inter-American Seaway and Proto-Caribbean Seaway) was a prehistoric body of water that once connected the Pacific Ocean to the Atlantic Ocean, separating North America from South America. It formed during the Jurassic (200–154 Ma) during the initial breakup of the supercontinent Pangaea into Laurasia and Gondwana, forming a mediterranean sea between the Panthalassia and Tethys Ocean, and finally closed when the Isthmus of Panama was formed by volcanic activity in the late Pliocene (2.76–2.54 Ma). The modern-day remnants of the seaway are the Gulf of Mexico, Caribbean Sea and the Central Atlantic region around the Sargasso Sea.

The closure of the Central American Seaway had tremendous effects on oceanic circulation and the biogeography of the adjacent seas, isolating many species and triggering speciation and diversification of tropical and sub-tropical marine fauna. The inflow of nutrient-rich water of deep Pacific origin into the Caribbean was blocked and so local species had to adapt to an environment of lower productivity. It had an even larger impact on terrestrial life. The seaway had isolated South America for much of the Cenozoic, which allowed the evolution of a wholly unique diverse mammalian fauna there. When it closed, a faunal exchange with North America ensued and led to the extinction of many of the native South American forms.

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Jurassic in the context of Relative ages

Relative dating is the science of determining the relative order of past events (i.e., the age of an object in comparison to another), without necessarily determining their absolute age (i.e., estimated age). In geology, rock or superficial deposits, fossils and lithologies can be used to correlate one stratigraphic column with another. Prior to the discovery of radiometric dating in the early 20th century, which provided a means of absolute dating, archaeologists and geologists used relative dating to determine ages of materials. Though relative dating can only determine the sequential order in which a series of events occurred, not when they occurred, it remains a useful technique. Relative dating by biostratigraphy is the preferred method in paleontology and is, in some respects, more accurate. The Law of Superposition, which states that older layers will be deeper in a site than more recent layers, was the summary outcome of 'relative dating' as observed in geology from the 17th century to the early 20th century.

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