Lingula Temporal range: | |
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Lingula anatina, shell (top), full habitus (bottom) | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Brachiopoda |
Class: | Lingulata |
Order: | Lingulida |
Family: | Lingulidae |
Genus: | Lingula Bruguière, 1791 |
Type species | |
Lingula anatina Lamarck, 1801 [1] | |
Species | |
| |
Synonyms | |
Ligula, Ligularius, Lingularius, Pharetra |
Lingula is a genus of brachiopods within the class Lingulata. Lingula or forms very close in appearance have existed possibly since the Cambrian. Like its relatives, it has two unadorned organo-phosphatic valves and a long fleshy stalk. Lingula lives in burrows in barren sandy coastal seafloor and feeds by filtering detritus from the water. It can be detected by a short row of three openings through which it takes in water (sides) and expels it again (middle).
A shell encloses the organs and other internal parts of the body, except for a long, fleshy stalk (or pedicle) that extends from the tail (or posterior) end of the shell. This shell has two nearly identical tan or bronze valves, that are often tinged greenish or bluegreenish. These are held together by muscles between them. The valves are secreted by two mantle folds, one on the dorsal and one on the ventral side of the body. The valves are composed of chitin, protein, and calcium phosphate and consist of about 50% organic material. The outer surface is covered by a thin glossy layer of protein called periostracum. The high organic content of the shell makes it somewhat soft and flexible. These valves are located on the dorsal and ventral surfaces of the animal. The front (or anterior) end of the shell has a squared off (or truncate) shape and the rear end tapers to a point where the stalk emerges. This point (called apex) is the earliest part of the valve. The shell of the young animal roughly remains the same, adding much material at the front and less at the sides. Many growth lines are visible, parallel to the margins of the shell. The valves widen slightly at the front end, forming a narrow opening (or gape), through which water is pumped in at the sides and out from the middle. The ventral valve is slightly longer and slightly more convex. The margin of the valves is fringed by chitinous tan colored bristle (or chaetae), short at the side of the valves, but much longer at the front where they assist in keeping open the access of the body cavity to the outside water. In death, the gape is closed and the bristles may be absent or short as they become brittle and darker in color when dry. [2]
The stalk (or pedicle) is a long white extension of the body, that emerges at the apex from between the valves, and not, as in articulate brachiopods, from a special opening in the dorsal valve. At the rear end, that is deepest in the sea bed, the skin (or epithelium) secretes a glue-like mucus that binds to the substrate's particles, thus temporarily anchoring the animal. The very thick skin (cuticle) is not composed of cells, and is opaque, being secreted by a very thin white epidermis, which is attached by a very thin layer of connective tissue to the white muscle inside. The muscle fibres are attached to the connective tissue and are wound like helixes. In the centre of the muscle runs an inconspicuous tube-shaped opening along the entire length, which is an extension of, and in open connection with, the body cavity within the shell. It is lined by a layer of one cell thick mesothelium. [2]
Ovaries have a fine texture and a tan to orange color. Male gonads are coarse-grained and creamy white. [3]
Species such as Lingula anatina have a breeding season that extends from summer to fall and breed annually. Their larvae are planktonic. [4]
Lingula has long been considered an example of a living fossil; in fact, the perceived longevity of this genus led Darwin to coin this concept. This living fossil status is now considered unjustified. This status is based on the shape of the shell only, and it has been shown that this shape corresponds to a burrowing lifestyle, occurring in different brachiopod lineages, with different and evolving internal structures. [1]
The genus Lingula was created in 1791 by Jean Guillaume Bruguière. George Shaw describe Mytilus rostrum in 1798, but this species was later assigned to Lingula. In 1801 Jean-Baptiste Lamarck described L. anatina, its type species. [1]
Lingula is probably derived from the Latin word for tongue "lingua" and a diminutive suffix -ula, so small tongue. Alternatively it may be derived from the Latin word for spoon (Lingula) directly. The origin of the epithet anatina is not known, but in Latin "anatina" means "belonging to the duck", possibly due to its resemblance to a duck bill. Another possible derivation could be from the French anatife ('goose barnacle'), for its likeness. [1]
The following species, previously assigned to Lingula are now considered better placed in other genera: [5]
The following are extinct Lingula species. [6]
Extinct Glottidia or Lingula species:
Lingula inhabits a vertical burrow in soft sediments, with the front face upward near the surface of the sea bed. The cilia on the lophophore create a current through the mantle cavity, which ensures the supply of food particles and oxygen. [2] Although Lingula is one of the most euryhaline brachiopods, it tolerates only moderate salinity variations (down to about half seawater salt concentration) and is optimally marine. [7] [8]
It is eaten in various parts of the world, such as Vietnam. Because they live in mud, they first need to be cleansed in fresh water. The most popular part is the stalk, which is crunchy to eat. They are also fermented. [9]
Lingulata is a class of brachiopods, among the oldest of all brachiopods having existed since the Cambrian period. They are also among the most morphologically conservative of the brachiopods, having lasted from their earliest appearance to the present with very little change in shape. Shells of living specimens found today in the waters around Japan are almost identical to ancient Cambrian fossils.
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 Craniidae are a family of brachiopods, the only surviving members of the subphylum Craniiformea. They are the only members of the order Craniida, the monotypic suborder Craniidina, and the superfamily Cranioidea; consequently, the latter two taxa are at present redundant and rarely used.There are three living genera within Craniidae: Neoancistrocrania, Novocrania, and Valdiviathyris. As adults, craniids either live freely on the ocean floor or, more commonly, cement themselves onto a hard object with all or part of the ventral valve.
Lingula reevii is an inarticulated brachiopod species assigned to the family Lingulidae. L. reevii is rare and is known to occur in shallow, sandy reef flats in Kaneohe Bay, Oahu, Hawaii, as well as in Japan, and Ambon, Indonesia.
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.
Acrotretides (Acrotretida) are an extinct order of linguliform brachiopods in the class Lingulata. Acrotretida contains 8 families within the sole superfamily Acrotretoidea. They lived from the Lower Cambrian to the Middle Devonian, rapidly diversifying during the middle Cambrian. In the upper Cambrian, linguliforms reached the apex of their diversity: acrotretides and their relatives the lingulides together comprised nearly 70% of brachiopod genera at this time. Though acrotretides continued to diversify during the Ordovician, their proportional dominance declined, as rhynchonelliforms took on a larger role in brachiopod faunas.
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.
Lingula anatina is a brachiopod species in the genus Lingula. Like others in its genus, L. anatina is a filter feeder that uses a lophophore to extract food from water. They burrow in the sand of their brackish intertidal habitat.
Crania is an extinct genus of brachiopods that lived during the Upper Cretaceous.
Mickwitziids are a Cambrian group of shelly fossils with originally phosphatic valves, belonging to the Brachiopod stem group, and exemplified by the genus Mickwitzia – the other genera are Heliomedusa and Setatella. The family Mickwitziidae is conceivably paraphyletic with respect to certain crown-group brachiopods.
Paterinata is an extinct class of linguliform brachiopods which lived from the lower Cambrian ("Tommotian") to the Upper Ordovician (Hirnantian). It contains the single order Paterinida and the subfamily Paterinoidea. Despite being some of the earliest brachiopods to appear in the fossil record, paterinides stayed as a relatively subdued and low-diversity group even as other brachiopods diversified later in the Cambrian and Ordovician. Paterinides are notable for their high degree of convergent evolution with rhynchonelliform (articulate) brachiopods, which have a similar set of muscles and hinge-adjacent structures.
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.
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.
Siphonotretida is an extinct order of linguliform brachiopods in the class Lingulata. The order is equivalent to the sole superfamily Siphonotretoidea, itself containing the sole family Siphonotretidae. Siphonotretoids were originally named as a superfamily of Acrotretida, before being raised to their own order.
Kutorginates (Kutorginata) are an extinct class of early rhynchonelliform ("articulate") brachiopods. The class contains only a single order, Kutorginida (kutorginides). Kutorginides were among the earliest rhynchonelliforms, restricted to the lower-middle part of the Cambrian Period.
The orthotetides (Orthotetida) are an extinct order of brachiopods in the class Strophomenata. Though not particularly diverse or abundant relative to strophomenides (Strophomenida) or productides (Productida), orthotetides were nevertheless the longest-lasting order of strophomenates, surviving from the Middle Ordovician (“Llanvirn”) up until the Late Permian. Externally, many orthotetides are difficult to distinguish from strophomenides. Most fundamental differences between the two orders are internal: orthotetides have more elaborate cardinal processes and a greater diversity of shell microstructure.
Terebratalia is a genus of brachiopods belonging to the family Terebrataliidae.
Terebratalia transversa or the North Pacific Lampshell is a species of marine brachiopod in the family Terebrataliidae. A two-valved shelled species, they are most frequently found in tidal habitats in the Pacific Northwest of the United States.