Tetragraptus approximatus Temporal range: | |
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Illustration of Tetragraptus approximatus | |
Original illustrations of Tetragraptus approximatus by Nicholson (1873). At the top is a magnified section of the stipes. A complete specimen is illustrated below. | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Hemichordata |
Class: | Pterobranchia |
Order: | † Graptoloidea |
Family: | † Dichograptidae |
Genus: | † Tetragraptus |
Species: | †T. approximatus |
Binomial name | |
†Tetragraptus approximatus Nicholson, 1873 | |
Tetragraptus approximatus is a species of dichograptid graptolite belonging to the genus Tetragraptus . It existed during the Floian Age (477.7 million years ago) of the Ordovician. It is an important index fossil in biostratigraphy.
The general outline of each Tetragraptus approximatus colony (rhabdosome) is highly distinctive. It resembles a long narrow letter H or X. The central process (the funicle) is about 2.5 mm (0.098 in) long, each end bifurcating at right angles with each other. Each pair of branches (stipes) curve away sharply from the ends of the funicle then run more or less parallel with each other at a distance of 5 to 8 mm (0.20 to 0.31 in) apart. Each of the stipes can reach more than 45 mm (1.8 in) in length, with approximately ten cup-like structures (thecae) for every 10 mm (0.39 in) of the stipes. The thecae are tilted at a 45° angle to the axis. [1] [2]
Tetragraptus approximatus is classified under the genus Tetragraptus of the family Dichograptidae. [3] [4] It was first described by the British paleontologist Henry Alleyne Nicholson in 1873 from specimens recovered from Lévis, Quebec, Canada. [2]
Tetragraptus approximatus is found worldwide. It has been identified in graptoliferous rocks from Australia, New Zealand, Canada (Newfoundland), the United States (Texas), Kazakhstan, Russia (Taimyr), China, South America, Norway, and Sweden. It is unknown, however, in areas which lack coeval graptoliferous rocks like the United Kingdom, Spitsbergen, and Africa. [5]
Tetragraptus approximatus is used in biostratigraphy as an index fossil. Its first appearance at the GSSP section of the Diabasbrottet Quarry in Västergötland, Sweden is defined as the beginning of the Floian Age (477.7 million years ago) of the Ordovician. [5]
The Cambrian is the first geological period of the Paleozoic Era, and the Phanerozoic Eon. The Cambrian lasted 53.4 million years from the end of the preceding Ediacaran period 538.8 Ma to the beginning of the Ordovician Period 485.4 Ma.
The Ordovician is a geologic period and system, the second of six periods of the Paleozoic Era, and the second of twelve periods of the Phanerozoic Eon. The Ordovician spans 41.6 million years from the end of the Cambrian Period 485.4 Ma to the start of the Silurian Period 443.8 Ma.
The Silurian is a geologic period and system spanning 24.6 million years from the end of the Ordovician Period, at 443.8 million years ago (Mya), to the beginning of the Devonian Period, 419.2 Mya. The Silurian is the third and shortest period of the Paleozoic Era, and the third of twelve periods of the Phanerozoic Eon. As with other geologic periods, the rock beds that define the period's start and end are well identified, but the exact dates are uncertain by a few million years. The base of the Silurian is set at a series of major Ordovician–Silurian extinction events when up to 60% of marine genera were wiped out.
Graptolites are a group of colonial animals, members of the subclass Graptolithina within the class Pterobranchia. These filter-feeding organisms are known chiefly from fossils found from the Middle Cambrian through the Lower Carboniferous (Mississippian). A possible early graptolite, Chaunograptus, is known from the Middle Cambrian. Recent analyses have favored the idea that the living pterobranch Rhabdopleura represents an extant graptolite which diverged from the rest of the group in the Cambrian.
Biostratigraphy is the branch of stratigraphy which focuses on correlating and assigning relative ages of rock strata by using the fossil assemblages contained within them. The primary objective of biostratigraphy is correlation, demonstrating that a particular horizon in one geological section represents the same period of time as another horizon at a different section. Fossils within these strata are useful because sediments of the same age can look completely different, due to local variations in the sedimentary environment. For example, one section might have been made up of clays and marls, while another has more chalky limestones. However, if the fossil species recorded are similar, the two sediments are likely to have been laid down around the same time. Ideally these fossils are used to help identify biozones, as they make up the basic biostratigraphy units, and define geological time periods based upon the fossil species found within each section.
Chitinozoa are a group of flask-shaped, organic walled marine microfossils produced by an as yet unknown organism. Common from the Ordovician to Devonian periods, the millimetre-scale organisms are abundant in almost all types of marine sediment across the globe. This wide distribution, and their rapid pace of evolution, makes them valuable biostratigraphic markers.
The Early Ordovician is the first epoch of the Ordovician period, corresponding to the Lower Ordovician series of the Ordovician system. It began after the Age 10 of the Furongian epoch of the Cambrian and lasted from 485.4 ± 1.9 to 470 ± 1.4 million years ago, until the Dapingian age of the Middle Ordovician. It includes Tremadocian and Floian ages.
John William Salter was an English naturalist, geologist, and palaeontologist.
The Tremadocian is the lowest stage of Ordovician. Together with the later Floian Stage it forms the Lower Ordovician Epoch. The Tremadocian lasted from 485.4 to 477.7 million years ago. The base of the Tremadocian is defined as the first appearance of the conodont species Iapetognathus fluctivagus at the Global Boundary Stratotype Section and Point (GSSP) section on Newfoundland.
The geology of the Australian Capital Territory includes rocks dating from the Ordovician around 480 million years ago, whilst most rocks are from the Silurian. During the Ordovician period the region—along with most of eastern Australia—was part of the ocean floor. The area contains the Pittman Formation consisting largely of quartz-rich sandstone, siltstone and shale; the Adaminaby Beds and the Acton Shale.
The Diabasbrottet Quarry, located on Mt. Hunneberg, Västergötland, Sweden, is the location of the Global Boundary Stratotype Section and Point (GSSP) which marks the lower boundary of the Floian stage of the Lower Ordovician.
In geology, the Arenig is a time interval during the Ordovician period and also the suite of rocks which were deposited during this interval.
The Floian is the second stage of the Ordovician Period. It succeeds the Tremadocian with which it forms the Lower Ordovician series. It precedes the Dapingian Stage of the Middle Ordovician. The Floian extended from 477.7 to 470 million years ago. The lower boundary is defined as the first appearance of the graptolite species Tetragraptus approximatus.
Dawsonia campanulata is an organic-walled Palaeozoic organism of unknown affinity. It resembles a shell or purse.
Didymograptus is an extinct genus of graptolites with four rows of cups. They lived during the Middle Ordovician, to Late Ordovician.
Tetragraptus is an extinct genus of graptolites from the Ordovician period.
Flo is a historic parish (socken) in the Swedish province of Västergötland. Since 1971 it has been a part of Grästorp Municipality.
Monograptidae is an extinct family of graptolites of the order Graptoloidea. Monograptids have only one row of thecae per stipe, unlike the biserial graptolites which have two opposing rows of thecae per stipe.
Labechiida is an extinct order of stromatoporoid sponges. They lived from the Early Ordovician to the Late Devonian, though a few putative fossils have been reported from younger sediments. Labechiids were the first order of stromatoporoids to appear and were probably ancestral to all other orders in the main Paleozoic radiation. They were most diverse and abundant during the Middle-Late Ordovician and the Famennian, when they were a major group of reef-building sponges. However, they were relatively uncommon through most of the Silurian and Devonian, in contrast to other stromatoporoids.