Pelagodiscus | |
---|---|
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Brachiopoda |
Order: | Discinida |
Family: | Discinidae |
Genus: | Pelagodiscus Dall, 1908 |
Species: | P. atlanticus |
Binomial name | |
Pelagodiscus atlanticus (King, 1868) | |
Pelagodiscus is a monospecific genus of discinid brachiopods. Silica tablets leave a distinctive tesselating imprint on the inner surface of its shell. [1]
Tentaculites is an extinct genus of conical fossils of uncertain affinity, class Tentaculita, although it is not the only member of the class. It is known from Lower Ordovician to Upper Devonian deposits both as calcitic shells with a brachiopod-like microstructure and carbonaceous 'linings'. The "tentaculites" are also referred to as the styliolinids.
Craniata is a class of brachiopods originating in the Cambrian period and still extant today. It is the only class within the subphylum Craniiformea, one of three major subphyla of brachiopods alongside linguliforms and rhynchonelliforms. Craniata is divided into three orders: the extinct Craniopsida and Trimerellida, and the living Craniida, which provides most information on their biology. Living members of the class have shells which are composed of calcite, though some extinct forms my have aragonite shells. The shells are inarticulate and are usually rounded in outline. There is no pedicle; the rear edge of the body cavity is a smooth and flat wall perforated by the anus. This class of brachiopods has an unsupported lophophore with only a single row of tentacles. In the absence of a pedicle, the shell is usually attached directly to a hard substrate. Many craniiforms are encrusting animals which attach directly to the shell of another animal, usually another brachiopod. The plicae from the host brachiopod will then appear within the shell of the craniiform.
The Obolellata are a class of Rhynchonelliform brachiopods with two orders, Obolellida and Naukatida. They are essentially restricted to the lower-middle Cambrian.
Linguliformea is a subphylum of inarticulate brachiopods. These were the earliest of brachiopods, ranging from the Cambrian into the Holocene. They rapidly diversified during the Cambrian into the Ordovician, but most families became extinct by the end of the Devonian.
Terebratula is a modern genus of brachiopods with a fossil record dating back to the "Late Devonian". These brachiopods are stationary epifaunal suspension feeders and have a worldwide distribution.
Discinisca is a genus of brachiopods with fossils dating back from the Early Devonian to the Pliocene of Africa, Europe, North America, and New Zealand.
The Mesozoic marine revolution (MMR) refers to the increase in shell-crushing (durophagous) and boring predation in benthic organisms throughout the Mesozoic era, along with bulldozing and sediment remodelling in marine habitats. The term was first coined by Geerat J. Vermeij, who based his work on that of Steven M. Stanley. While the MMR was initially restricted to the Cretaceous, more recent studies have suggested that the beginning of this ecological/evolutionary arms race extends as far back as the Triassic, with the MMR now being considered to have started in the Anisian or the Aalenian. It is an important transition between the Palaeozoic evolutionary fauna and the Modern evolutionary fauna that occurred throughout the Mesozoic.
Strophomenida is an extinct order of articulate brachiopods which lived from the lower Ordovician period to the mid Carboniferous period. Strophomenida is part of the extinct class Strophomenata, and was the largest known order of brachiopods, encompassing over 400 genera. Some of the largest and heaviest known brachiopod species belong to this class. Strophomenids were among the most diverse and abundant brachiopods during the Ordovician, but their diversity was strongly impacted at the Late Ordovician mass extinction. Survivors rediversified into new morphologies in the Silurian, only to be impacted once again at the Late Devonian mass extinction. However, they still survived till the end of the Permian.
Brachiopods, phylum Brachiopoda, are a phylum of trochozoan animals that have hard "valves" (shells) on the upper and lower surfaces, unlike the left and right arrangement in bivalve molluscs. Brachiopod valves are hinged at the rear end, while the front can be opened for feeding or closed for protection. Two major categories are traditionally recognized, articulate and inarticulate brachiopods. The word "articulate" is used to describe the tooth-and-groove structures of the valve-hinge which is present in the articulate group, and absent from the inarticulate group. This is the leading diagnostic skeletal feature, by which the two main groups can be readily distinguished as fossils. Articulate brachiopods have toothed hinges and simple, vertically oriented opening and closing muscles. Conversely, inarticulate brachiopods have weak, untoothed hinges and a more complex system of vertical and oblique (diagonal) muscles used to keep the two valves aligned. In many brachiopods, a stalk-like pedicle projects from an opening near the hinge of one of the valves, known as the pedicle or ventral valve. The pedicle, when present, keeps the animal anchored to the seabed but clear of sediment which would obstruct the opening.
The origin of the brachiopods is uncertain; they either arose from reduction of a multi-plated tubular organism, or from the folding of a slug-like organism with a protective shell on either end. Since their Cambrian origin, the phylum rose to a Palaeozoic dominance, but dwindled during the Mesozoic.
The Kirengellids are a group of problematic Cambrian fossil shells of marine organisms. The shells bear a number of paired muscle scars on the inner surface of the valve.
Rhynchonelliformea is a major subphylum and clade of brachiopods. It is roughly equivalent to the former class Articulata, which was used previously in brachiopod taxonomy up until the 1990s. These so-called articulated brachiopods have many anatomical differences relative to "inarticulate" brachiopods of the subphyla Linguliformea and Craniformea. Articulates have hard calcium carbonate shells with tongue-and-groove hinge articulations and separate sets of simple opening and closing muscles.
Discinidae is a family in the brachiopod superfamily Discinoidea. Unlike most brachiopods, which have uniformly calcitic or phosphatic shells, modern-day discinids incorporate tablets of silica into their valves. These are covered with vesicles into which the siliceous tablets are cemented, much like a closely packed mosaic, and held together with apatite. These vesicles eventually degrade, but nevertheless still leave an imprint on the shell itself. It has been suggested that this siliceous biomineralisation might also have occurred amongst some of the earliest Paleozoic brachiopods because similar patterns of shell imprints have been observed amongst them too.
Trimerellida is an extinct order of craniate brachiopods, containing the sole superfamily Trimerelloidea and the families Adensuidae, Trimerellidae, and Ussuniidae. Trimerellidae was a widespread family of warm-water brachiopods ranging from the Middle Ordovician to the late Silurian (Ludlow). Adensuidae and Ussuniidae are monogeneric families restricted to the Ordovician of Kazakhstan. Most individuals were free-living, though some clustered into large congregations similar to modern oyster reefs.
Discinida is an order of brachiopods comprising the extant superfamily Discinoidea, and the extinct superfamilies Botsfordioidea (early—mid-Cambrian) and Acrotheloidea. It represents a sister taxon to the Lingulids, and is possibly paraphyletic with respect to the Acrotretoids.—or the acrotretids are paraphyletic with respect to it. The group displays a broad range of shell structures, some of which incorporate substantial organic or silicified components.
Argyrotheca is a genus of very small to minute lampshells. All species share a large pedicel opening, one ridge on the inside of the pedunculate valve, pits in a diamond pattern on the inside of both valves, and without radial ridges that end in tubercles. It occurs in depths between 6 and 1300 m. It is known since the latest Cretaceous.
Acrotheloidea is a superfamily of Discinid brachiopods, alternatively ascribed to the lingulids—for a discussion of discinid taxonomy, see Discinida.
Botsfordioidea is a superfamily of Discinid brachiopods.
Strophomenata is an extinct class of brachiopods in the subphylum Rhynchonelliformea.
Rafinesquina is an extinct genus of large brachiopod that existed from the Darriwilian to the Ludlow epoch.