Cretaceous in the context of Chalk


Cretaceous in the context of Chalk

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Cretaceous 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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Cretaceous in the context of Apulian Plate

The Adriatic or Apulian plate is a small tectonic plate carrying primarily continental crust that broke away from the African plate along a large transform fault in the Cretaceous period. The name Adriatic plate is usually used when referring to the northern part of the plate. This part of the plate was deformed during the Alpine orogeny, when the Adriatic/Apulian plate collided with the Eurasian plate.

The Adriatic/Apulian plate is thought to still move independently of the Eurasian plate in NNE direction with a small component of counter-clockwise rotation. The fault zone that separates the two is the Periadriatic Seam that runs through the Alps. Studies indicate that in addition to deforming, the Eurasian continental crust has actually subducted to some extent below the Adriatic/Apulian plate, an unusual circumstance in plate tectonics. Oceanic crust of the African plate is also subducting under the Adriatic/Apulian plate off the western and southern coasts of the Italian Peninsula, creating a berm of assorted debris which rises from the seafloor and continues onshore. This subduction is also responsible for the volcanic interactions of southern Italy.

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Cretaceous 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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Cretaceous in the context of Karaburun Peninsula, Albania

The Karaburun Peninsula (Albanian: Gadishulli i Karaburunit), also known as Cape Linguetta, is a peninsula of the Mediterranean Sea located in Southern and Southeastern Europe, which is almost completely surrounded by both the Adriatic Sea to the north and the Ionian Sea to the south. It is located in Southwestern Albania along the Albanian Ionian Sea Coast, whereas the Strait of Otranto separates it from Italy. The Strait of Mezokanal separates the peninsula from Sazan Island, while in the southeast stretches the Bay of Vlorë. In classical antiquity, its name was the "Akrokeraunian Peninsula" (Ακροκεραύνιο ακρωτήριο), whose name was derived from the eponymous Akrokeraunian mountains; this is because, in terms of geology, the Rrëza e Kanalit on the peninsula represent the continuation of said mountains, which are the highest and most extensive mountain range system that extends parallel to the Ionian Sea. Karaburun peninsula is sometimes called Ceraunian Peninsula due to the name of the mountain range. Formed during the mesozoic era of the cretaceous and paleogene period, the crests of the mountain range form a northwest-southeast line with a series of distinct peaks along its irregular structure that are broken apart by steep and unequally slopes. The highest peaks are namely, the Maja Çaderës, Maja e Flamurit, Maja e Koretës and Maja e Ilqes.

The western section comprises a rough relief and is dotted with sandy and rocky beaches, sea caves, steep cliffs and several bays amongst them Cave of Haxhi Ali, Cape of Gjuhëz, Bay of Skaloma, Bay of Arushë, Bay of Dafinë, and most notably Bay of Grama, where ships and vessels anchored during classical antiquity. On the high and steep rock faces of the bay, which served also as a marble quarry, there are hundreds of rock inscriptions dating back to the 4th century BC.

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Cretaceous in the context of 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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Cretaceous in the context of Maastricht

Maastricht (/ˈmɑːstrɪxt/ MAH-strikht, US also /mɑːˈstrɪxt/ mah-STRIKHT, Dutch: [maːˈstrɪxt] ; Limburgish: Mestreech [məˈstʀeːx]) is a city and a municipality in the southeastern Netherlands. It is the capital and largest city of the province of Limburg. Maastricht is located on both sides of the Meuse (Dutch: Maas), at the point where the river is joined by the Jeker. Mount Saint Peter (Sint-Pietersberg) is largely situated within the city's municipal borders. Maastricht is adjacent to the border with Belgium and is part of the Meuse-Rhine Euroregion, an international metropolis with a population of about 3.9 million, which includes the nearby German and Belgian cities of Aachen, Liège, and Hasselt.

Maastricht developed from a Roman settlement (Trajectum ad Mosam) to a medieval river trade and religious centre. In the 16th century it became a garrison town and in the 19th century an early industrial centre. Today, the city is a thriving cultural and regional hub. It became well known through the Maastricht Treaty and as the birthplace of the euro. Maastricht has 1,677 national heritage buildings (rijksmonumenten), the second highest number in the Netherlands, after Amsterdam. The city is visited by tourists for shopping and recreation, and has a large international student population. The last stage of the Cretaceous period and the Mesozoic era, the Maastrichtian, is named after this city, at the end of which was the Cretaceous–Paleogene extinction event, which resulted in the extinction of the non-avian dinosaurs.

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Cretaceous in the context of Ant

Ants are eusocial insects of the family Formicidae and, along with the related wasps and bees, belong to the order Hymenoptera. Ants evolved from vespoid wasp ancestors in the Cretaceous period. More than 13,800 of an estimated total of 22,000 species have been classified. They are easily identified by their geniculate (elbowed) antennae and the distinctive node-like structure that forms their slender waists.

Ants form colonies that range in size from a few dozen individuals often living in small natural cavities to highly organised colonies that may occupy large territories with a sizeable nest (or nests) that consist of millions of individuals, in some cases they reach hundreds of millions of individuals in super colonies. Typical colonies consist of various castes of sterile, wingless females, most of which are workers (ergates), as well as soldiers (dinergates) and other specialised groups. Nearly all ant colonies also have some fertile males called "drones" and one or more fertile females called "queens" (gynes). The colonies are described as superorganisms because the ants appear to operate as a unified entity, collectively working together to support the colony.

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Cretaceous 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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Cretaceous in the context of Oomycete

The Oomycetes (/ˌ.əˈmsts/), or Oomycota, form a distinct phylogenetic lineage of fungus-like eukaryotic microorganisms within the Stramenopiles. They are filamentous and heterotrophic, and can reproduce both sexually and asexually. Sexual reproduction of an oospore is the result of contact between hyphae of male antheridia and female oogonia; these spores can overwinter and are known as resting spores. Asexual reproduction involves the formation of chlamydospores and sporangia, producing motile zoospores. Oomycetes occupy both saprophytic and pathogenic lifestyles, and include some of the most notorious pathogens of plants, causing devastating diseases such as late blight of potato and sudden oak death. One oomycete, the mycoparasite Pythium oligandrum, is used for biocontrol, attacking plant pathogenic fungi. The oomycetes are also often referred to as water molds (or water moulds), although the water-preferring nature which led to that name is not true of most species, which are terrestrial pathogens.

Oomycetes were originally grouped with fungi due to similarities in morphology and lifestyle. However, molecular and phylogenetic studies revealed significant differences between fungi and oomycetes which means the latter are now grouped with the stramenopiles (which include some types of algae). The Oomycota have a very sparse fossil record; a possible oomycete has been described from Cretaceous amber.

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Cretaceous in the context of Angiosperm

Flowering plants are plants that bear flowers and fruits, and form the clade Angiospermae (/ˌæniəˈspɜːrm/). The term angiosperm is derived from the Greek words ἀγγεῖον (angeion; 'container, vessel') and σπέρμα (sperma; 'seed'), meaning that the seeds are enclosed within a fruit. The group was formerly called Magnoliophyta.

Angiosperms are by far the most diverse group of land plants with 64 orders, 416 families, approximately 13,000 known genera and 300,000 known species. They include all forbs (flowering plants without a woody stem), grasses and grass-like plants, a vast majority of broad-leaved trees, shrubs and vines, and most aquatic plants. Angiosperms are distinguished from the other major seed plant clade, the gymnosperms, by having flowers, xylem consisting of vessel elements instead of tracheids, endosperm within their seeds, and fruits that completely envelop the seeds. The ancestors of flowering plants diverged from the common ancestor of all living gymnosperms before the end of the Carboniferous, over 300 million years ago. In the Cretaceous, angiosperms diversified explosively, becoming the dominant group of plants across the planet.

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Cretaceous in the context of Conifer

Conifers (/ˈkɒnɪfər/) are a group of seed plants, a subset of gymnosperms. They are mainly evergreen trees with a regular branching pattern, reproducing with male and female cones, usually on the same tree. They are wind-pollinated and the seeds are usually dispersed by the wind. Scientifically, they make up the division Pinophyta, also known as Coniferae. All extant conifers except for the Gnetophytes are perennial woody plants with secondary growth. There are over 600 living species.

Conifers first appear in the fossil record over 300 million years ago in the Carboniferous. They became dominant land plants in the Mesozoic, until flowering plants took over many ecosystems in the Cretaceous. Many conifers today are relict species, surviving in a small part of their former ranges. Such relicts include Wollemia, known only from a small area of Australia, and Metasequoia glyptostroboides, known from Cretaceous fossils and surviving in a small area of China.

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Cretaceous 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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Cretaceous 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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Cretaceous in the context of Seabird

Seabirds (also known as marine birds) are birds that are adapted to life within the marine environment. While seabirds vary greatly in lifestyle, behaviour and physiology, they often exhibit striking convergent evolution, as the same environmental problems and feeding niches have resulted in similar adaptations. The first seabirds evolved in the Cretaceous period, while modern seabird families emerged in the Paleogene.

Seabirds generally live longer, breed later and have fewer young than other birds, but they invest a great deal of time in their young. Most species nest in colonies, varying in size from a few dozen birds to millions. Many species are famous for undertaking long annual migrations, crossing the equator or circumnavigating the Earth in some cases. They feed both at the ocean's surface and below it, and even on each other. Seabirds can be highly pelagic, coastal, or in some cases spend a part of the year away from the sea entirely.

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Cretaceous in the context of Crocodilia

Crocodilia (/krɒkəˈdɪliə/) is an order of semiaquatic, predatory reptiles that are known as crocodilians. They appeared 83.5 million years ago in the Late Cretaceous period (Campanian stage) and are the closest living relatives of birds, as the two groups are the only known survivors of the Archosauria. Members of the crocodilian total group, the clade Pseudosuchia, appeared about 250 million years ago in the Early Triassic period, and diversified during the Mesozoic era. The order includes the true crocodiles (family Crocodylidae), the alligators and caimans (family Alligatoridae), and the gharial and false gharial (family Gavialidae). Although the term "crocodiles" is sometimes used to refer to all of these families, the term "crocodilians" is less ambiguous.

Extant crocodilians have flat heads with long snouts and tails that are compressed on the sides, with their eyes, ears, and nostrils at the top of the head. Alligators and caimans tend to have broader U-shaped jaws that, when closed, show only the upper teeth, whereas crocodiles usually have narrower V-shaped jaws with both rows of teeth visible when closed. Gharials have extremely slender, elongated jaws. The teeth are conical and peg-like, and the bite is powerful. All crocodilians are good swimmers and can move on land in a "high walk" position, traveling with their legs erect rather than sprawling. Crocodilians have thick skin covered in non-overlapping scales and, like birds, have a four-chambered heart and lungs with unidirectional airflow.

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Cretaceous in the context of Late Cretaceous

The Late Cretaceous (100.5–66 Ma) is the more recent of two epochs into which the Cretaceous Period is divided in the geologic time scale. Rock strata from this epoch form the Upper Cretaceous Series. The Cretaceous is named after creta, the Latin word for the white limestone known as chalk. The chalk of northern France and the white cliffs of south-eastern England date from the Cretaceous Period.

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Cretaceous in the context of Cretaceous–Paleogene extinction event

The Cretaceous–Paleogene (K–Pg) extinction event, formerly known as the Cretaceous-Tertiary (K–T) extinction event, was a major mass extinction of three-quarters of the plant and animal species on Earth approximately 66 million years ago. The event caused the extinction of all non-avian dinosaurs. Most other tetrapods weighing more than 25 kg (55 lb) also became extinct, with the exception of some ectothermic species such as sea turtles and crocodilians. It marked the end of the Cretaceous period, and with it the Mesozoic era, while heralding the beginning of the current geological era, the Cenozoic Era. In the geologic record, the K–Pg event is marked by a thin layer of sediment called the K–Pg boundary or K–T boundary, which can be found throughout the world in marine and terrestrial rocks. The boundary clay shows unusually high levels of the metal iridium, which is more common in asteroids than in the Earth's crust.

As originally proposed in 1980 by a team of scientists led by Luis Alvarez and his son Walter, it is now generally thought that the K–Pg extinction resulted from the impact of a massive asteroid 10 to 15 km (6 to 9 mi) wide, 66 million years ago, causing the Chicxulub impact crater and devastating the global environment, mainly through a lingering impact winter which halted photosynthesis in plants and plankton. The impact hypothesis, also known as the Alvarez hypothesis, was bolstered by the discovery of the 180 km (112 mi) Chicxulub crater in the Gulf of Mexico's Yucatán Peninsula in the early 1990s. The temporal match between the ejecta layer, and the onset of the extinctions and the agreement of ecological patterns in the fossil record with modeled environmental perturbations (for example, darkness and cooling), lead to the conclusion that the Chicxulub impact triggered the mass extinction. A 2016 drilling project into the Chicxulub peak ring confirmed that the peak ring comprised granite ejected within minutes from deep in the Earth, but contained hardly any gypsum, the usual sulfate-containing sea floor rock in the region: the gypsum would have vaporized and dispersed as an aerosol into the atmosphere, causing longer-term effects on the climate and food chain. In October 2019, researchers proposed the mechanisms of the mass extinction, arguing that the Chicxulub asteroid impact event rapidly acidified the oceans and produced long-lasting effects on the climate.

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Cretaceous 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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