Rugosa Temporal range: | |
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Solitary rugose coral Grewingkia canadensis in three views; Ordovician, Indiana | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Cnidaria |
Class: | Hexacorallia |
Subclass: | † Rugosa Milne Edwards & Haime 1850 [1] |
Suborders | |
The Rugosa, also called the Tetracorallia, rugose corals, or horn corals, are an extinct order of solitary and colonial corals that were abundant in Middle Ordovician to Late Permian seas. [3]
Solitary rugosans (e.g., Caninia , Lophophyllidium , Neozaphrentis , Streptelasma ) are often referred to as horn corals because of a unique horn-shaped chamber with a wrinkled, or rugose, wall. Some solitary rugosans reached nearly a meter (3 ft 3 in) in length. However, some species of rugose corals could form large colonies (e.g., Lithostrotion ). When radiating septa were present, they were usually in multiples of four, hence Tetracorallia in contrast to modern Hexacorallia , colonial polyps generally with sixfold symmetry.
Rugose corals have a skeleton made of calcite that is often fossilized. Like modern corals (Scleractinia), rugose corals were invariably benthic, living on the sea floor or in a reef-framework. Some symbiotic rugose corals were endobionts of Stromatoporoidea, especially in the Silurian period. [4] [5] Although there is no direct proof, it is inferred that these Palaeozoic corals possessed stinging cells to capture prey. They also had tentacles to help them catch prey. Technically they were carnivores, but prey-size was so small they are often referred to as microcarnivores.
Rugose corals always show tabulae, horizontal plates that divide the corallite skeleton. The corallites are usually large relative to different types of coral. Rugose corals will sometimes have dissepiments, which are curved plates connected to septa and tabulae. The symmetry can be distinguished by the orientation of septa in a transverse section of the coral. Rugose corals always display bilateral symmetry whereas tabulate and scleractinian corals show radial symmetry. Initially there are only four major septa; later minor septa are added in the four resulting spaces. The complex arrangement of septa is diagnostic of rugose corals. Rugose corals will also always have a columella, an axial rod which supports the septa running up the center of the corallite. It is present in rugose corals because they were mainly solitary and so required the extra support. Tabulate corals have no columella because they were always colonial and relied on the support of neighboring corallites. [6]
Corals are colonial marine invertebrates within the class Anthozoa of the phylum Cnidaria. They typically form compact colonies of many identical individual polyps. Coral species include the important reef builders that inhabit tropical oceans and secrete calcium carbonate to form a hard skeleton.
Anthozoa is a class of marine invertebrates which includes the sea anemones, stony corals and soft corals. Adult anthozoans are almost all attached to the seabed, while their larvae can disperse as part of the plankton. The basic unit of the adult is the polyp; this consists of a cylindrical column topped by a disc with a central mouth surrounded by tentacles. Sea anemones are mostly solitary, but the majority of corals are colonial, being formed by the budding of new polyps from an original, founding individual. Colonies are strengthened by calcium carbonate and other materials and take various massive, plate-like, bushy or leafy forms.
Scleractinia, also called stony corals or hard corals, are marine animals in the phylum Cnidaria that build themselves a hard skeleton. The individual animals are known as polyps and have a cylindrical body crowned by an oral disc in which a mouth is fringed with tentacles. Although some species are solitary, most are colonial. The founding polyp settles and starts to secrete calcium carbonate to protect its soft body. Solitary corals can be as much as 25 cm (10 in) across but in colonial species the polyps are usually only a few millimetres in diameter. These polyps reproduce asexually by budding, but remain attached to each other, forming a multi-polyp colony of clones with a common skeleton, which may be up to several metres in diameter or height according to species.
Bioerosion describes the breakdown of hard ocean substrates – and less often terrestrial substrates – by living organisms. Marine bioerosion can be caused by mollusks, polychaete worms, phoronids, sponges, crustaceans, echinoids, and fish; it can occur on coastlines, on coral reefs, and on ships; its mechanisms include biotic boring, drilling, rasping, and scraping. On dry land, bioerosion is typically performed by pioneer plants or plant-like organisms such as lichen, and mostly chemical or mechanical in nature.
Tabulata, commonly known as tabulate corals, are an order of extinct forms of coral. They are almost always colonial, forming colonies of individual hexagonal cells known as corallites defined by a skeleton of calcite, similar in appearance to a honeycomb. Adjacent cells are joined by small pores. Their distinguishing feature is their well-developed horizontal internal partitions (tabulae) within each cell, but reduced or absent vertical internal partitions. They are usually smaller than rugose corals, but vary considerably in shape, from flat to conical to spherical.
Stromatoporoidea is an extinct clade of sea sponges common in the fossil record from the Middle Ordovician to the Late Devonian. They can be characterized by their densely layered calcite skeletons lacking spicules. Stromatoporoids were among the most abundant and important reef-builders of their time, living close together in flat biostromes or elevated bioherms on soft tropical carbonate platforms.
A corallite is the skeletal cup, formed by an individual stony coral polyp, in which the polyp sits and into which it can retract. The cup is composed of aragonite, a crystalline form of calcium carbonate, and is secreted by the polyp. Corallites vary in size, but in most colonial corals they are less than 3 mm (0.12 in) in diameter. The inner surface of the corallite is known as the calyx. The vertical blades inside the calyx are known as septa and in some species, these ridges continue outside the corallite wall as costae. Where there is no corallite wall, the blades are known as septocostae. The septa, costae and septocostae may have ornamentation in the form of teeth and may be thick, thin or variable in size. Sometimes there are paliform lobes, in the form of rods or blades, rising from the inner margins of the septa. These may form a neat circle called the paliform crown. The septa do not usually unite in the centre of the corallite, instead they form a columella, a tangled mass of intertwined septa, or a dome-shaped or pillar-like projection. In the living coral, the lower part of the polyp is in intimate contact with the corallite, and has radial mesenteries between the septa which increase the surface area of the body cavity and aid digestion. The septa, palliform lobes and costae can often be seen through the coenosarc, the layer of living tissue that covers the coenosteum, the part of the skeleton between the corallites.
Mussidae is a family of stony coral in the order Scleractinia. Following a taxonomic revision in 2012, the family is now restricted to species found in the Atlantic Ocean, with Pacific species transferred to the new family Lobophylliidae. Many species are referred to as brain coral because their generally spheroid form and grooved surface resembles the convolutions of a brain.
Cornulitida is an extinct order of encrusting animals from class Tentaculita, which were common around the globe in the Ordovician to Devonian oceans, and survived until the Carboniferous. Organisms that may be the oldest cornulitids have been found in Cambrian sediments of Jordan.
Anticalyptraea is a fossil genus of encrusting tentaculitoid tubeworms from the Silurian to Devonian of Europe and North America . Anticalyptraea commonly encrust various invertebrate fossils such as stromatoporoids, rugose corals, bryozoans, brachiopods and crinoids, but they can also be common on the hardgrounds.
Chaetosalpinx is an ichnogenus of bioclaustrations. Chaetosalpinx includes straight to sinuous cavities that are parallel to the host's axis of growth. The cavity is circular to oval in cross-section and it lacks a wall lining or floor-like tabulae. They are common in tabulate and rugose corals from Late Ordovician to Devonian of Europe and North America. They may have been parasites.
Lobactis is a genus of plate or mushroom coral in the family Fungiidae. The genus is monotypic with a single species, Lobactis scutaria, that is found in the Indo-Pacific region.
Turbinaria peltata, commonly known as disc coral, is a species of colonial stony coral in the family Dendrophylliidae. It is native to the Indo-Pacific region. The International Union for Conservation of Nature has rated its conservation status as being "vulnerable".
Dactylotrochus is a genus of large polyp stony corals from the Red Sea and western Pacific Ocean. It is monotypic with a single species, Dactylotrochus cervicornis. It inhabits the deep sea and is believed to be azooxanthellate.
Schizocyathus is a monotypic genus of stony corals in the family Schizocyathidae, the only species being Schizocyathus fissilis. It is a deep water, azooxanthellate coral.
Olev Vinn is an Estonian paleobiologist and paleontologist.
Pseudoamplexus is an extinct genus of horn corals belonging to the order Rugosa.
Phaulactis is an extinct genus of rugose coral that existed during the Ordovician, Silurian and Devonian periods. It can be found in Europe, North America, Asia and Australia. Phaulactis was described by Ryder in 1926.
Goniophyllum is an Silurian genus of rugose coral known from Sweden, Norway, Canada, the United Kingdom and the United States. It is easily identified by its "lids" and distinct square shape. The genus was described by Milne-Edwards et Haime in 1851.