brachiopod

File:Brachiopod valves and pedicle (articulate) 01 svg.svg

Modern brachiopods range from {{convert|1|to|100|mm}} long, and most species are about {{convert|10|to|30|mm}}.{{sfn|Cohen: Brachiopoda ELS|(2002)}} Magellania venosa is the largest extant species.{{cite journal | url=https://pubmed.ncbi.nlm.nih.gov/29690189/ | pmid=29690189 | year=2018 | last1=Araya | first1=J. F. | last2=Bitner | first2=M. A. | title=Rediscovery of Terebratulina austroamericana Zezina, 1981 (Brachiopoda: Cancellothyrididae) from off northern Chile | journal=Zootaxa | volume=4407 | issue=3 | pages=443–446 | doi=10.11646/zootaxa.4407.3.11 }} The largest brachiopods known—Gigantoproductus and Titanaria, reaching {{convert|30|to|38|cm}} in width—occurred in the upper part of the Lower Carboniferous.{{cite book|last= Moore|first= R.C.|year= 1965|title= Brachiopoda|publisher= Geological Society of America/University of Kansas Press|series= Treatise on Invertebrate Paleontology|volume= Part H., Volume I|pages= H440|location= Boulder, Colorado/Lawrence, Kansas|isbn= 978-0-8137-3015-8}} Brachiopods have two valves (shell sections), which cover the dorsal (top) and ventral (bottom) surface of the animal, unlike bivalve molluscs whose shells cover the lateral surfaces (sides). The valves are unequal in size and structure, with each having its own symmetrical form rather than the two being mirror images of each other. The formation of brachiopod shells during ontogeny builds on a set of conserved genes, including homeobox genes, that are also used to form the shells of molluscs.{{Cite journal |last1=Wernström |first1=Joel Vikberg |last2=Gąsiorowski |first2=Ludwik |last3=Hejnol |first3=Andreas |date=2022-09-19 |title=Brachiopod and mollusc biomineralisation is a conserved process that was lost in the phoronid–bryozoan stem lineage |journal=EvoDevo |volume=13 |issue=1 |pages=17 |doi=10.1186/s13227-022-00202-8 |issn=2041-9139 |pmc=9484238 |pmid=36123753 |doi-access=free }}

The brachial valve is usually smaller and bears brachia ("arms") on its inner surface. These brachia are the origin of the phylum's name, and support the lophophore, used for feeding and respiration. The pedicle valve is usually larger, and near the hinge it has an opening for the stalk-like pedicle through which most brachiopods attach themselves to the substrate. (R. C. Moore, 1952) The brachial and pedicle valves are often called the dorsal and ventral valves, respectively, but some paleontologists regard the terms "dorsal" and "ventral" as irrelevant since they believe that the "ventral" valve was formed by a folding of the upper surface under the body. The ventral ("lower") valve actually lies above the dorsal ("upper") valve when most brachiopods are oriented in life position. In many living articulate brachiopod species, both valves are convex, the surfaces often bearing growth lines and/or other ornamentation. However, inarticulate lingulids, which burrow into the seabed, have valves that are smoother, flatter and of similar size and shape. (R. C. Moore, 1952)

Articulate ("jointed") brachiopods have a tooth and socket arrangement by which the pedicle and brachial valves hinge, locking the valves against lateral displacement. Inarticulate brachiopods have no matching teeth and sockets; their valves are held together only by muscles. (R. C. Moore, 1952)

All brachiopods have adductor muscles that are set on the inside of the pedicle valve and which close the valves by pulling on the part of the brachial valve ahead of the hinge. These muscles have both "quick" fibers that close the valves in emergencies and "catch" fibers that are slower but can keep the valves closed for long periods. Articulate brachiopods open the valves by means of abductor muscles, also known as diductors, which lie further to the rear and pull on the part of the brachial valve behind the hinge. Inarticulate brachiopods use a different opening mechanism, in which muscles reduce the length of the coelom (main body cavity) and make it bulge outwards, pushing the valves apart. Both classes open the valves to an angle of about 10 degrees. The more complex set of muscles employed by inarticulate brachiopods can also operate the valves as scissors, a mechanism that lingulids use to burrow.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

{{Annotated image | float=right | image=Lingula anatina.jpg | width=200 | image-width=200 | height=100 | image-top=-50

| caption=The inarticulate species Lingula anatina, showing the long pedicle, flattened shells and prominent chaetae around the front edge of the shells

|annotations=

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Each valve consists of three layers, an outer periostracum made of organic compounds and two biomineralized layers. Articulate brachiopods have an outermost periostracum made of proteins, a "primary layer" of calcite (a form of calcium carbonate) under that, and innermost a mixture of proteins and calcite.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Inarticulate brachiopod shells have a similar sequence of layers, but their composition is different from that of articulated brachiopods and also varies among the classes of inarticulate brachiopods. The Terebratulida are an example of brachiopods with a punctate shell structure; the mineralized layers are perforated by tiny open canals of living tissue, extensions of the mantle called caeca, which almost reach the outside of the primary layer. These shells can contain half of the animal's living tissue. Impunctate shells are solid without any tissue inside them. Pseudopunctate shells have tubercles formed from deformations unfurling along calcite rods. They are only known from fossil forms, and were originally mistaken for calcified punctate structures.[http://species-identification.org/species.php?species_group=brachiopoda&selected=foto&menuentry=inleiding&record=Morphology Marine Species Identification Portal : Brachiopoda of the North Sea]{{Cite book |last=Copper |first=Paul |url=https://books.google.com/books?id=JHVUDwAAQBAJ&dq=%2522punctate+brachiopods%2522&pg=PA2185 |title=Brachiopods |year=2018 |publisher=Routledge |isbn=978-1-351-46309-6 |language=en}}

Lingulids and discinids, which have pedicles, have a matrix of glycosaminoglycans (long, unbranched polysaccharides), in which other materials are embedded: chitin in the periostracum;{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} apatite containing calcium phosphate in the primary biomineralized layer;"Apatite" is strictly defined in terms of its structure rather than chemical composition. Some forms contain calcium phosphate and others have calcium carbonate. See {{cite web|url=http://www.uwex.edu/wgnhs/Mineral%20Index/Minerals/apatite.htm|title=Apatite Ca5(PO4, CO3)3(F, Cl, OH) Hexagonal|last=Cordua|first=W.S.|publisher=University of Wisconsin|access-date=23 October 2009|archive-url=https://web.archive.org/web/20090830001131/http://www.uwex.edu/wgnhs/Mineral%20Index/Minerals/apatite.htm|archive-date=30 August 2009|url-status=dead}} and a complex mixture in the innermost layer, containing collagen and other proteins, chitinophosphate and apatite.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}} Craniids, which have no pedicle and cement themselves directly to hard surfaces, have a periostracum of chitin and mineralized layers of calcite.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}{{sfn|Parkinson etc: Brachiopod shells|(2005)}} Shell growth can be described as holoperipheral, mixoperipheral, or hemiperipheral. In holoperipheral growth, distinctive of craniids, new material is added at an equal rate all around the margin. In mixoperipheral growth, found in many living and extinct articulates, new material is added to the posterior region of the shell with an anterior trend, growing towards the other shell. Hemiperipheral growth, found in lingulids, is similar to mixoperipheral growth but occurs in mostly a flat plate with the shell growing forwards and outwards.{{Cite book | url = https://books.google.com/books?id=SfnSesBc-RgC&q=mixoperipheral&pg=PA303|title=Glossary of Geology|isbn=9780922152766|last1=Neuendorf|first1=Klaus K. E.|last2=Institute|first2=American Geological|year=2005|publisher=Springer }}

Brachiopods, as with molluscs, have an epithelial mantle which secretes and lines the shell, and encloses the internal organs. The brachiopod body occupies only about one-third of the internal space inside the shell, nearest the hinge. The rest of the space is lined with the mantle lobes, extensions that enclose a water-filled space in which sits the lophophore.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The coelom (body cavity) extends into each lobe as a network of canals, which carry nutrients to the edges of the mantle.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}}

Relatively new cells in a groove on the edges of the mantle secrete material that extends the periostracum. These cells are gradually displaced to the underside of the mantle by more recent cells in the groove, and switch to secreting the mineralized material of the shell valves. In other words, on the edge of the valve the periostracum is extended first, and then reinforced by extension of the mineralized layers under the periostracum.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} In most species the edge of the mantle also bears movable bristles, often called chaetae or setae, that may help defend the animals and may act as sensors. In some brachiopods groups of chaetae help to channel the flow of water into and out of the mantle cavity.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

In most brachiopods, diverticula (hollow extensions) of the mantle penetrate through the mineralized layers of the valves into the periostraca. The function of these diverticula is uncertain and it is suggested that they may be storage chambers for chemicals such as glycogen, may secrete repellents to deter organisms that stick to the shell or may help in respiration.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Experiments show that a brachiopod's oxygen consumption drops if petroleum jelly is smeared on the shell, clogging the diverticula.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}}

File:Terebratalia transversa 115544343.jpg, a modern brachiopod in the order Terebratulida]]

Like bryozoans and phoronids, brachiopods have a lophophore, a crown of tentacles whose cilia (fine hairs) create a water current that enables them to filter food particles out of the water. However a bryozoan or phoronid lophophore is a ring of tentacles mounted on a single, retracted stalk,{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Bryozoa"|pp=829–845}}{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Phoronida"|pp=817–821}} while the basic form of the brachiopod lophophore is U-shaped, forming the brachia ("arms") from which the phylum gets its name.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Brachiopod lophophores are non-retractable and occupy up to two-thirds of the internal space, in the frontmost area where the valves gape when opened. To provide enough filtering capacity in this restricted space, lophophores of larger brachiopods are folded in moderately to very complex shapes—loops and coils are common, and some species' lophophores contort into a shape resembling a hand with the fingers splayed.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} In all species the lophophore is supported by cartilage and by a hydrostatic skeleton (in other words, by the pressure of its internal fluid),{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} and the fluid extends into the tentacles.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Some articulate brachiopods also have a brachidium, a calcareous support for the lophophore attached to the inside of the brachial valve,{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} which have led to an extremely reduced lophophoral muscles and the reduction of some brachial nerves.{{cite journal | doi=10.1038/s41598-021-95584-5 | title=The nervous system of the most complex lophophore provides new insights into the evolution of Brachiopoda | year=2021 | last1=Temereva | first1=Elena N. | last2=Kuzmina | first2=Tatyana V. | journal=Scientific Reports | volume=11 | issue=1 | page=16192 | pmid=34376709 | pmc=8355163 | bibcode=2021NatSR..1116192T }}

The tentacles bear cilia (fine mobile hairs) on their edges and along the center. The beating of the outer cilia drives a water current from the tips of the tentacles to their bases, where it exits. Food particles that collide with the tentacles are trapped by mucus, and the cilia down the middle drive this mixture to the base of the tentacles.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Introduction"|p=817}} A brachial groove runs round the bases of the tentacles, and its own cilia pass food along the groove towards the mouth.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The method used by brachiopods is known as "upstream collecting", as food particles are captured as they enter the field of cilia that creates the feeding current. This method is used by the related phoronids and bryozoans, and also by pterobranchs. Entoprocts use a similar-looking crown of tentacles, but it is solid and the flow runs from bases to tips, forming a "downstream collecting" system that catches food particles as they are about to exit.{{sfn|Riisgård etc: Downstream|(2000)}}

File:Lingulid burrow 01.png

{{anchor|pedicle}}Most modern species attach to hard surfaces by means of a cylindrical pedicle ("stalk"), an extension of the body wall. This has a chitinous cuticle (non-cellular "skin") and protrudes through an opening in the hinge.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} However, some genera have no pedicle, such as the inarticulate Crania and the articulate Lacazella; they cement the rear of the "pedicle" (ventral) valve to a surface so that the front is slightly inclined up away from the surface.{{sfn|Cohen: Brachiopoda ELS|(2002)}}{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} In these brachiopods, the ventral valve lacks a pedicle opening.{{cite web|url=http://paleo.cortland.edu/tutorial/Brachiopods/brachmorph.htm|title=Brachiopodia Morphology and Ecology |last=Wells|first=Roger M.|work=Invertebrate Paleontology Tutorial|publisher=State University of New York College at Courtland|access-date=6 March 2010|archive-url=https://web.archive.org/web/20100620183917/http://paleo.cortland.edu/tutorial/Brachiopods/brachmorph.htm|archive-date=20 June 2010|url-status=dead}} In a few articulate genera such as Neothyris and Anakinetica, the pedicles wither as the adults grow and finally lie loosely on the surface. In these genera the shells are thickened and shaped so that the opening of the gaping valves is kept free of the sediment.{{sfn|Cohen: Brachiopoda ELS|(2002)}}

Pedicles of inarticulate species are extensions of the main coelom, which houses the internal organs. A layer of longitudinal muscles lines the epidermis of the pedicle.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Members of the order Lingulida have long pedicles, which they use to burrow into soft substrates, to raise the shell to the opening of the burrow to feed, and to retract the shell when disturbed.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} A lingulid moves its body up and down the top two-thirds of the burrow, while the remaining third is occupied only by the pedicle, with a bulb on the end that builds a "concrete" anchor.{{sfn|Emig: Inart Brach|(2001)}} However, the pedicles of the order Discinida are short and attach to hard surfaces.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

The pedicle of articulate brachiopods has no coelom, and its homology is unclear. It is constructed from a different part of the larval body, and has a compact core composed of connective tissue. Muscles at the rear of the body can straighten, bend or even rotate the pedicle. The far end of the pedicle generally has rootlike extensions or short papillae ("bumps"), which attach to hard surfaces. However, articulate brachiopods of the genus Chlidonophora use a branched pedicle to anchor in sediment. The pedicle emerges from the pedicle valve, either through a notch in the hinge or, in species where the pedicle valve is longer than the brachial, from a hole where the pedicle valve doubles back to touch the brachial valve. Some species stand with the front end upwards, while others lie horizontal with the pedicle valve uppermost.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

Some early brachiopods—for example strophomenates, kutorginates and obolellates—do not attach using their pedicle, but with an entirely different structure known as the "pedicle sheath", which has no relationship to the pedicle.{{Cite journal|last1=Holmer|first1=LE|last2=Zhang|first2=Z|last3=Topper|first3=TP|last4=Popov|first4=L|title=The attachment strategies of Cambrian kutorginate brachiopods: the curious case of two pedicle openings and their phylogenetic significance|journal=Journal of Paleontology|volume=92|pages=33–39|doi=10.1017/jpa.2017.76|year=2018|issue=1 |bibcode=2018JPal...92...33H |s2cid=134399842}}{{cite journal |author= Bassett, M.G. and Popov, L.E. |date= 2017 |title= Earliest ontogeny of the Silurian orthotetide brachiopod Coolinia and its significance for interpreting strophomenate phylogeny |journal= Lethaia |volume= 50 |issue= 4 |pages= 504–510 |doi= 10.1111/let.12204|bibcode= 2017Letha..50..504B }} This structure arises from the umbo of the pedicle valve, at the centre of the earliest (metamorphic) shell at the location of the protegulum. It is sometimes associated with a fringing plate, the colleplax.

File:Liospiriferina rostrata Noir.jpg

File:Rhynchonellid crura Permian Texas.JPG (Middle Permian); Glass Mountains, Texas]]

The water flow enters the lophophore from the sides of the open valves and exits at the front of the animal. In lingulids the entrance and exit channels are formed by groups of chaetae that function as funnels.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} In other brachiopods the entry and exit channels are organized by the shape of the lophophore.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} The lophophore captures food particles, especially phytoplankton (tiny photosynthetic organisms), and deliver them to the mouth via the brachial grooves along the bases of the tentacles.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The mouth is a tiny slit at the base of the lophophore.{{sfn|Cohen etc: Brachiopod fold|(2003)}} Food passes through the mouth, muscular pharynx ("throat") and oesophagus ("gullet"),{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} all of which are lined with cilia and cells that secrete mucus and digestive enzymes.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} The stomach wall has branched ceca ("pouches") where food is digested, mainly within the cells.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

Nutrients are transported throughout the coelom, including the mantle lobes, by cilia.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} The wastes produced by metabolism are broken into ammonia, which is eliminated by diffusion through the mantle and lophophore.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Brachiopods have metanephridia, used by many phyla to excrete ammonia and other dissolved wastes. However, brachiopods have no sign of the podocytes, which perform the first phase of excretion in this process,{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Bilateria" sect. "Excretion"|pp=212–214}} and brachiopod metanephridia appear to be used only to emit sperm and ova.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

The majority of food consumed by brachiopods is digestible, with very little solid waste produced.{{sfn|Cowen: History of life|(2000)|loc=ch. "Invert Paleo"|p=408}} The cilia of the lophophore can change direction to eject isolated particles of indigestible matter. If the animal encounters larger lumps of undesired matter, the cilia lining the entry channels pause and the tentacles in contact with the lumps move apart to form large gaps and then slowly use their cilia to dump the lumps onto the lining of the mantle. This has its own cilia, which wash the lumps out through the opening between the valves. If the lophophore is clogged, the adductors snap the valves sharply, which creates a "sneeze" that clears the obstructions.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} In some inarticulate brachiopods the digestive tract is U-shaped and ends with an anus that eliminates solids from the front of the body wall.{{sfn|Cohen etc: Brachiopod fold|(2003)}} Other inarticulate brachiopods and all articulate brachiopods have a curved gut that ends blindly, with no anus.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} These animals bundle solid waste with mucus and periodically "sneeze" it out, using sharp contractions of the gut muscles.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}}

The lophophore and mantle are the only surfaces that absorb oxygen and eliminate carbon dioxide. Oxygen seems to be distributed by the fluid of the coelom, which is circulated through the mantle and driven either by contractions of the lining of the coelom or by beating of its cilia. In some species oxygen is partly carried by the respiratory pigment hemerythrin, which is transported in coelomocyte cells.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The maximum oxygen consumption of brachiopods is low, and their minimum requirement is not measurable.

Brachiopods also have colorless blood, circulated by a muscular heart lying in the dorsal part of the body above the stomach.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The blood passes through vessels that extend to the front and back of the body, and branch to organs including the lophophore at the front and the gut, muscles, gonads and nephridia at the rear. The blood circulation seems not to be completely closed, and the coelomic fluid and blood must mix to a degree.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} The main function of the blood may be to deliver nutrients.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

The "brain" of adult articulates consists of two ganglia, one above and the other below the oesophagus. Adult inarticulates have only the lower ganglion.{{sfn|Nielsen: Brachio brains|(2005)}} From the ganglia and the commissures where they join, nerves run to the lophophore, the mantle lobes and the muscles that operate the valves. The edge of the mantle has probably the greatest concentration of sensors. Although not directly connected to sensory neurons, the mantle's chaetae probably send tactile signals to receptors in the epidermis of the mantle. Many brachiopods close their valves if shadows appear above them, but the cells responsible for this are unknown. Some brachiopods have statocysts, which detect changes in the animals' position.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

Lifespans range from 3 to over 30 years.{{sfn|Cohen: Brachiopoda ELS|(2002)}} Adults of most species are of one sex throughout their lives. The gonads are masses of developing gametes (ova or sperm), and most species have four gonads, two in each valve.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} Those of articulates lie in the channels of the mantle lobes, while those of inarticulates lie near the gut.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} Ripe gametes float into the main coelom and then exit into the mantle cavity via the metanephridia, which open on either side of the mouth. Most species release both ova and sperm into the water, but females of some species keep the embryos in brood chambers until the larvae hatch.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

The cell division in the embryo is radial (cells form in stacks of rings directly above each other), holoblastic (cells are separate, although adjoining) and regulative (the type of tissue into which a cell develops is controlled by interactions between adjacent cells, rather than rigidly within each cell).{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Bilateria" sect. "Reproduction"|pp=214–219}} While some animals develop the mouth and anus by deepening the blastopore, a "dent" in the surface of the early embryo, the blastopore of brachiopods closes up, and their mouth and anus develop from new openings.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}

The larvae of lingulids (Lingulida and Discinida) are planktotrophic (feeding), and swim as plankton for months{{sfn|Cohen: Brachiopoda ELS|(2002)}} resembling miniature adults, with valves, mantle lobes, a pedicle that coils in the mantle cavity, and a small lophophore, which is used for both feeding and swimming.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The larvae of craniids have no pedicle or shell.{{sfn|Doherty: Lophophorates|(2001)|loc=sect. "Introduction", "Brachiopoda"|pp=341–342, 356–363}} As the shell becomes heavier, the juvenile sinks to the bottom and becomes a sessile adult.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} The larvae of articulate species (Craniiformea and Rhynchonelliformea) are lecithotrophic (non-feeding) and live only on yolk, and remain among the plankton for only a few days. The Rhynchonelliformea larvae has three larval lobes, unlike the Craniiformea which only have two larval lobes.{{cite journal | pmc=5572269 | year=2017 | last1=Altenburger | first1=A. | last2=Martinez | first2=P. | last3=Budd | first3=G. E. | last4=Holmer | first4=L. E. | title=Gene Expression Patterns in Brachiopod Larvae Refute the "Brachiopod-Fold" Hypothesis | journal=Frontiers in Cell and Developmental Biology | volume=5 | page=74 | doi=10.3389/fcell.2017.00074 | pmid=28879180 | doi-access=free }}{{sfn|Cohen: Brachiopoda ELS|(2002)}} This type of larva has a ciliated frontmost lobe that becomes the body and lophophore, a rear lobe that becomes the pedicle, and a mantle like a skirt, with the hem towards the rear. On metamorphosing into an adult, the pedicle attaches to a surface, the front lobe develops the lophophore and other organs, and the mantle rolls up over the front lobe and starts to secrete the shell.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}} In cold seas, brachiopod growth is seasonal and the animals often lose weight in winter. These variations in growth often form growth lines in the shells. Members of some genera have survived for a year in aquaria without food.{{sfn|Cohen: Brachiopoda ELS|(2002)}}

{{Further|Taxonomy of the Brachiopoda}}

File:Pygites diphyoides (d'Orbigny).jpg (Orbigny, 1849) from the Hauterivian (Lower Cretaceous) of Cehegin, Murcia, Spain. This terebratulid is characterized by a central perforation through its valves.]]

Brachiopod fossils show great diversity in the morphology of the shells and lophophore, while the modern genera show less diversity but provide soft-bodied characteristics. Both fossils and extant species have limitations that make it difficult to produce a comprehensive classification of brachiopods based on morphology. The phylum also has experienced significant convergent evolution and reversals (in which a more recent group seems to have lost a characteristic that is seen in an intermediate group, reverting to a characteristic last seen in an older group). Hence some brachiopod taxonomists believe it is premature to define higher levels of classification such as order, and recommend instead a bottom-up approach that identifies genera and then groups these into intermediate groups.{{sfn|Carlson: Ghosts|(2001)}}

However, other taxonomists believe that some patterns of characteristics are sufficiently stable to make higher-level classifications worthwhile, although there are different views about what the higher-level classifications should be.{{sfn|Carlson: Ghosts|(2001)}}

The "traditional" classification was defined in 1869; two further approaches were established in the 1990s:{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}}{{sfn|ITIS: Brachiopoda}}

• In the "traditional" classification, brachiopods are divided into the Articulata and Inarticulata. The Articulata have toothed hinges between the valves, while the hinges of the Inarticulata are held together only by muscles.{{sfn|Ruppert etc: Invert Zoo|(2004)|loc=ch. "Lophophorata" sect. "Brachiopoda"|pp=821–829}}{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}}
• A classification devised in the 1990s, based on the materials of which the shells are based, united the Craniida and the "articulate" brachiopods in the Calciata, which have calcite shells. The Lingulida and Discinida, combined in the Lingulata, have shells made of chitin and calcium phosphate.{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}}
• A three-part scheme, also from the 1990s, places the Craniida in a separate group of its own, the Craniiformea. The Lingulida and Discinida are grouped as Linguliformea,{{Cite journal|last=Torres-Martínez, M.A., Sour-Tovar, F.|year=2016|title=Braquiópodos discínidos (Lingulida, Discinoidea) de la Formación Ixtaltepec, Carbonífero del área de Santiago Ixtaltepec, Oaxaca|journal=Boletín de la Sociedad Geológica Mexicana|volume=68|issue=2|pages=313–321|doi=10.18268/BSGM2016v68n2a9|doi-access=free|bibcode=2016BoSGM..68..313T }} and the Rhynchonellida and Terebratulida as Rhynchonelliformea.{{sfn|Milsom etc: 3-part taxonomy|(2009)}}{{sfn|Williams etc: Suprafamilial Classif|(2000)|loc=Preface|pp=xxxix-xlv}}

About 330 living species are recognized,{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}} grouped into over 100 genera. The great majority of modern brachiopods are rhynchonelliforms (Articulata).{{sfn|Cohen: Brachiopoda ELS|(2002)}}

Genetic analysis performed since the 1990s has extended the understanding of the relationship between different organisms. It is now clear the brachiopods do not belong to the Deuterostomia (such as echinoderms and chordates) as was hypothesized earlier, but should be included in the broad group Protostomia, in a subgroup now called Lophotrochozoa. Although their adult morphology seems rather different, the nucleotide sequence of the 18S rRNA indicates that the phoronids (horseshoe worms) are the closest relatives of the inarticulate brachiopods, more so than articulate brachiopods. For now, the weight of evidence is inconclusive as to the exact relations within the inarticulates. Consequently, it has been suggested to include horseshoe worms in the Brachiopoda as a class named Phoronata (B.L.Cohen & Weydmann) in addition to the Craniata and Lingulata, within the subphylum Linguliformea. The other subphylum, Rhynchonelliformea contains only one extant class, which is subdivided into the extant orders Rhynchonellida, Terebratulida and Thecideida.{{cite journal |first=B.L. |last=Cohen |date=7 February 2000 |title=Monophyly of brachiopods and phoronids |journal=Proceedings of the Royal Society B |volume=267 |issue=1440 |pages=225–231 |doi=10.1098/rspb.2000.0991 |pmid=10714876 |pmc=1690528}}{{cite journal |first1=Bernard L. |last1=Cohen |first2=Agata |last2=Weydmann |date=1 December 2005 |title=Molecular evidence that phoronids are a subtaxon of brachiopods (Brachiopoda: Phoronata) and that genetic divergence of metazoan phyla began long before the early Cambrian |journal=Organisms Diversity & Evolution |volume=5 |issue=4 |pages=253–273 |doi=10.1016/j.ode.2004.12.002 |bibcode=2005ODivE...5..253C |url=http://eprints.gla.ac.uk/2944/1/Phoronids.pdf}}

This shows the taxonomy of brachiopods down to the order level, including extinct groups, which make up the majority of species. Extinct groups are indicated with a (†) symbol:

• Class †Hyolitha{{Cite journal |last=Smith |first=Martin R |date=2019 |title=Finding a home for hyoliths |url=https://academic.oup.com/nsr/article/7/2/470/5644056 |access-date=2024-09-30 |journal=National Science Review |volume=7 |issue=2 |pages=470–471 |doi=10.1093/nsr/nwz194 |pmc=8288929 |pmid=34692061}}
• Order †Hyolithida
• Subphylum Linguliformea
• Class Lingulata
• Order Lingulida
• Order †Acrotretida
• Order †Siphonotretida
• Class †Paterinata
• Order †Paterinida
• Subphylum Craniiformea
• Class Craniata
• Order Craniida
• Order †Craniopsida
• Order †Trimerellida
• Subphylum Rhynchonelliformea
• Class †Chileata
• Order †Chileida
• Order †Dictyonellida
• Class †Obolellata
• Order †Obolellida
• Order †Naukatida
• Class †Kutorginata
• Order †Kutorginida
• Class †Strophomenata
• Order †Billingsellida
• Order †Strophomenida
• Order †Productida
• Order †Orthotetida
• Class Rhynchonellata
• Order Rhynchonellida
• Order Terebratulida
• Order Thecideida
• Order †Protorthida
• Order †Orthida
• Order †Pentamerida
• Order †Atrypida
• Order †Athyridida
• Order †Spiriferida
• Order †Spiriferinida

File:StrophomenidCornulitidOrdovician.jpg brachiopod with attached cornulitid worm tube (Upper Ordovician, SE Indiana, USA). Brachiopod valves often serve as substrates for encrusting organisms.]]

Brachiopods are an entirely marine phylum, with no known freshwater species. Most species avoid locations with strong currents or waves, and typical sites include rocky overhangs, crevices and caves, steep slopes of continental shelves, and in deep ocean floors. However, some articulate species attach to kelp or in exceptionally sheltered sites in intertidal zones. The smallest living brachiopod, Gwynia, is only about {{convert|1|mm}} long, and lives in between gravel grains.{{sfn|Cohen: Brachiopoda ELS|(2002)}} Rhynchonelliforms, whose larvae consume only their yolks and settle and develop quickly, are often endemic to an area and form dense populations that can reach thousands per meter. Young adults often attach to the shells of more mature ones. On the other hand, inarticulate brachiopods, whose larva swim for up to a month before settling, have wide ranges. Members of the discinoid genus Pelagodiscus have a cosmopolitan distribution.{{sfn|Cohen: Brachiopoda ELS|(2002)}}

Brachiopods have a low metabolic rate, between one third and one tenth of that of bivalves. While brachiopods were abundant in warm, shallow seas during the Cretaceous period, most of their former niches are now occupied by bivalves, and most now live in cold and low-light conditions.{{sfn|Vermeij: Directionality|(1999)}}

Brachiopod shells occasionally show evidence of damage by predators, and sometimes of subsequent repair. Fish and crustaceans seem to find brachiopod flesh distasteful.{{sfn|Cohen: Brachiopoda ELS|(2002)}} The fossil record shows that drilling predators like gastropods attacked molluscs and echinoids 10 to 20 times more often than they did brachiopods, suggesting that such predators attacked brachiopods by mistake or when other prey was scarce.{{sfn|Kowalewski etc: 2nd-choice prey|(2002)}} In waters where food is scarce, the snail Capulus ungaricus steals food from bivalves, snails, tube worms, and brachiopods.{{sfn|Iyengar: Kleptoparasitism|(2008)}}

Among brachiopods only the lingulids have been fished commercially, and only on a very small scale.{{sfn|UCMP: Lingulata}} It is mostly the fleshy pedicle that is eaten.[https://web.archive.org/web/20130114132919/http://news.hayfestival.org/post/24408796185/the-worlds-oldest-food-delicacy-revealed The world’s oldest food delicacy revealed][https://iopscience.iop.org/article/10.1088/1742-6596/1417/1/012039 The Potency and Food Safety of Lamp Shells (Brachiopoda: Lingula sp.) as Food Resources][https://books.google.com/books?id=KJBKC4qvV8AC&dq=sea+bean-sprout+edible+pedicle&pg=PA111 Applied Palaeontology][https://books.google.com/books?id=GRZEBgAAQBAJ&dq=%22brachiopod+Lingula+is+eaten+both+in+Fiji+%2C+Japan+and+the+Philippine+Islands%22&pg=PA202 Fishing in Many Waters] Brachiopods seldom settle on artificial surfaces, probably because they are vulnerable to pollution. This may make the population of Coptothyrus adamsi useful as a measure of environmental conditions around an oil terminal being built in Russia on the shore of the Sea of Japan.{{sfn|Zvyagintsev etc: Brachio fouling|(2007)}}

Brachiopods are the state fossil of the U.S. state of Kentucky.{{cite web |title=Kentucky's State Fossil: Brachiopods |url=https://www.uky.edu/KGS/education/state-fossil-brachiopods.php |website=Kentucky Geological Survey}}

{{clear right}}

{{Brachiopod major groups}}

File:Isocrania costata Sowerby 1823.jpg

{{Main|Evolution of brachiopods}}

Over 12,000 fossil species are recognized,{{sfn|Ax: Multicellular Animals|(2003)|loc=ch."Brachiopoda"|pp=87–93}} grouped into over 5,000 genera. While the largest modern brachiopods are {{convert|100|mm}} long,{{sfn|Cohen: Brachiopoda ELS|(2002)}} a few fossils measure up to {{convert|200|mm}} wide.{{sfn|Fortey: Fossils the key|(2008)|loc=ch. "How to recognize" sect. "Brachiopods"}} The earliest confirmed brachiopods have been found in the early Cambrian, inarticulate forms appearing first, followed soon after by articulate forms.{{sfn|Ushatinskaya: Earliest brachiopods|(2008)}} Three unmineralized species have also been found in the Cambrian, and apparently represent two distinct groups that evolved from mineralized ancestors.{{sfn|Balthasar etc: Brachios stem Phoronids|(2009)}} The inarticulate Lingula is often called a "living fossil", as very similar genera have been found all the way back to the Ordovician. On the other hand, articulate brachiopods have produced major diversifications, and suffered severe mass extinctions{{sfn|Fortey: Fossils the key|(2008)|loc=ch.

"How to recognize" sect. "Brachiopods"}}—but the articulate Rhynchonellida and Terebratulida, the most diverse present-day groups, appeared at the start of the Ordovician and Carboniferous, respectively.{{sfn|UCMP: Brachio Fossil Range}}

Since 1991 Claus Nielsen has proposed a hypothesis about the development of brachiopods, adapted in 2003 by Cohen and colleagues as a hypothesis about the earliest evolution of brachiopods. This "brachiopod fold" hypothesis suggests that brachiopods evolved from an ancestor similar to Halkieria,{{sfn|Cohen etc: Brachiopod fold|(2003)}} a slug-like animal with "chain mail" on its back and a shell at the front and rear end.{{sfn|Conway Morris etc: Articulated Halkieriids|(1995)}} The hypothesis proposes that the first brachiopod converted its shells into a pair of valves by folding the rear part of its body under its front.{{sfn|Cohen etc: Brachiopod fold|(2003)}}

However, fossils from 2007 onwards have supported a new interpretation of the Early-Cambrian tommotiids, and a new hypothesis that brachiopods evolved from tommotiids. The "armor mail" of tommotiids was well-known but not in an assembled form, and it was generally assumed that tommotiids were slug-like animals similar to Halkieria, except that tommotiids' armor was made of organophosphatic compounds while that of Halkieria was made of calcite. However, fossils of a new tommotiid, Eccentrotheca, showed an assembled mail coat that formed a tube, which would indicate a sessile animal rather than a creeping slug-like one. Eccentrotheca's organophosphatic tube resembled that of phoronids,{{Cite journal| first1 = C. B.| last2 = Brock| first2 = G. A.| last4 = Holmer| last3 = Paterson| last5 = Budd | first3 = J. R.| last1 = Skovsted| first4 = L. E.| first5 = G. E.| title = The scleritome of Eccentrotheca from the Lower Cambrian of South Australia: Lophophorate affinities and implications for tommotiid phylogeny| journal = Geology| volume = 36| issue = 2| pages = 171| year = 2008| doi = 10.1130/G24385A.1 |bibcode = 2008Geo....36..171S }} sessile animals that feed by lophophores and are regarded either very close relatives or a sub-group of brachiopods.{{sfn|Cohen: Phoronids in Brachios|(2000|)}} Paterimitra, another mostly assembled fossil found in 2008 and described in 2009, had two symmetrical plates at the bottom, like brachiopod valves but not fully enclosing the animal's body.{{Cite journal| last4 = Hogstrom| last1 = Skovsted| last2 = Holmer | first1 = C. B. | first2 = E.| first3 = M.| last6 = Topper| last3 = Larsson| last7 = Balthasar | first4 = E. | first5 = A.| last8 = Stolk| last9 = Paterson| last5 = Brock| first6 = P.| first7 = U.| first8 = P. | first9 = R.| title = The scleritome of Paterimitra: an Early Cambrian stem group brachiopod from South Australia| journal = Proceedings of the Royal Society B: Biological Sciences| volume = 276| issue = 1662| pages = 1651–1656| date=May 2009 | issn = 0962-8452| pmid = 19203919| pmc = 2660981| doi = 10.1098/rspb.2008.1655}}

File:Cincinnetina meeki (Miller, 1875) slab 2.jpg species Cincinnetina meeki (Miller, 1875)]]

At their peak in the Paleozoic,{{cite book

| url = https://books.google.com/books?id=bL60DwAAQBAJ&dq=largest+Gigantoproductus+giganteus&pg=PA47

| title = Convergent Evolution on Earth. Lessons for the Search for Extraterrestrial Life

| publisher = MIT Press

| date = 2019

| access-date = 2022-08-23

| page = 47

| author = George R. McGhee, Jr.

| isbn = 9780262354189

}} the brachiopods were among the most abundant filter-feeders and reef-builders,{{sfn|Barry: Great Dying|(2002)}} and occupied other ecological niches, including swimming in the jet-propulsion style of scallops.{{sfn|Cohen: Brachiopoda ELS|(2002)}} However, after the Permian–Triassic extinction event, informally known as the "Great Dying",{{sfn|Barry: Great Dying|(2002)}} brachiopods recovered only a third of their former diversity.{{sfn|Barry: Great Dying|(2002)}} It was often thought that brachiopods were actually declining in diversity, and that in some way bivalves out-competed them. However, in 1980, Gould and Calloway produced a statistical analysis that concluded that both brachiopods and bivalves increased all the way from the Paleozoic to modern times, but bivalves increased faster; the Permian–Triassic extinction was moderately severe for bivalves but devastating for brachiopods, so that brachiopods for the first time were less diverse than bivalves and their diversity after the Permian increased from a very low base; there is no evidence that bivalves out-competed brachiopods, and short-term increases or decreases for both groups appeared synchronously.{{sfn|Gould etc: Clams and Brachios|(1980)}} In 2007 Knoll and Bambach concluded that brachiopods were one of several groups that were most vulnerable to the Permian–Triassic extinction, as all had calcareous hard parts (made of calcium carbonate) and had low metabolic rates and weak respiratory systems.{{sfn|Knoll etc: P-Tr extinction|(2007)}}

Brachiopod fossils have been useful indicators of climate changes during the Paleozoic era. When global temperatures were low, as in much of the Ordovician, the large difference in temperature between equator and poles created different collections of fossils at different latitudes. On the other hand, warmer periods, such much of the Silurian, created smaller difference in temperatures, and all seas at the low to middle latitudes were colonized by the same few brachiopod species.{{sfn|Gaines etc: Inverteb proxies|(2009)}}

File:Productid Permian Texas.JPG); Glass Mountains, Texas]]

From about the 1940s to the 1990s, family trees based on embryological and morphological features placed brachiopods among or as a sister group to the deuterostomes.{{sfn|Halanych: New phylogeny|(2004)}}De Rosa (2001) cites the following examples of brachiopods as close to deuterostomes:

• {{cite book|last=Hyman|first=L.H.|title=The invertebrates|url=https://archive.org/details/invertebratespro0000unse|url-access=registration|publisher=McGraw-Hill|year=1940|isbn=978-0-07-031661-4}}
• {{cite journal|last=Eernisse|first=D.J. |author2=Albert, J.S. |author3=Anderson, F.E.|year=1992|title=Annelida and Arthropoda are not sister taxa: A phylogenetic analysis of spiralian metazoan morphology|journal=Systematic Biology|volume=41|issue=3 |pages=305–330|doi=10.1093/sysbio/41.3.305}}
• {{cite book|last=Nielsen|first=C.|title=Animal evolution: Interrelationships of the living phyla|url=https://archive.org/details/animalevolutioni0000niel|url-access=registration|publisher=Oxford University Press|year=1995|isbn=978-0-19-854867-6}}
• {{cite journal|last=Lüter|first=C.|author2=Bartholomaeus, T.|title=The phylogenetic position of Brachiopoda—a comparison of morphological and molecular data|journal=Zoologica Scripta|volume=26|pages=245–253|doi=10.1111/j.1463-6409.1997.tb00414.x|date=July 1997|issue=3|s2cid=83934233}}

a super-phylum that includes chordates and echinoderms.{{sfn|UCMP: Deuterostomia}} Closer examination has found difficulties in the grounds on which brachiopods were affiliated with deuterostomes:

• Radial cleavage in the earliest divisions of the egg appears to be the original condition for the ancestral bilaterians, in the earliest Ecdysozoa and possibly in the earliest Eutrochozoa, a major sub-group of the Lophotrochozoa.{{sfn|Valentine: Cleavage patterns|(1997)}} Hence radial cleavage does not imply that brachiopods are affiliated with deuterostomes.
• The traditional view is that the coelom(s) in deuterostomes and protostomes form by different process, called enterocoely and schizocoely, respectively. However, research since the early 1990s has found significant exceptions.{{sfn|Valentine: Cleavage patterns|(1997)}}
• {{cite book|last=Ruppert|first=E.E|title=Microscopic anatomy of invertebrates, volume 4: Aschelminthes|editor=Harrison, F.W. |editor2=Ruppert, E.E|publisher=Wiley-Liss|year=1991|pages=1–17|chapter=Introduction to the aschelminth phyla: A consideration of mesoderm, body cavities, and cuticle}}
• {{cite journal|doi=10.1111/j.1469-185X.1999.tb00046.x|last=Budd|first=G.E|author2=Jensen, S|date=May 2000|title=A critical reappraisal of the fossil record of the bilaterian phyla|journal=Biological Reviews of the Cambridge Philosophical Society|volume=75|pages=253–295|pmid=10881389|issue=2|s2cid=39772232}} Both types of coelom construction appear among brachiopods, and therefore do not imply that brachiopods are deuterostomes.
• The terms "deuterostomes" and "protostomes" originally defined distinct ways of forming the mouth from the blastopore, a depression that appears in an early stage of the embryo. However, some "protostomes" form the mouth using a process more like that typical of deuterostomes.{{cite book|last=Anderson|first=D.T.|title=Embryology and phylogeny in annelids and arthropods|publisher=Pergamon Press Ltd|year=1973|isbn=978-0-08-017069-5}}{{cite journal|last=Arendt|first=D.|author2=Nubler-Jung, K.|year=1997|title=Dorsal or ventral: Similarities in fate maps and gastrulation patterns in annelids, arthropods and chordates|journal=Mechanisms of Development|volume=71|issue=1–2|pages=7–21|doi=10.1016/S0925-4773(96)00620-X |pmid=9076674|s2cid=14964932|doi-access=free}} Hence forming the mouth via a deuterostome-like process does not imply that brachiopods are affiliated with deuterostomes.

Nielsen views the brachiopods and closely related phoronids as affiliated with the deuterostome pterobranchs because their lophophores are driven by one cilium per cell, while those of bryozoans, which he regards as protostomes, have multiple cilia per cell.{{sfn|Nielsen: Phylog pos of Brachios|(2002)}} However, pterobranchs are hemichordates and probably closely related to echinoderms, and there is no evidence that the latest common ancestor of pterobranchs and other hemichordates or the latest common ancestor of hemichordates and echinoderms was sessile and fed by means of tentacles.

From 1988 onwards analyses based on molecular phylogeny, which compares biochemical features such as similarities in DNA, have placed brachiopods among the Lophotrochozoa, a protostome super-phylum that includes molluscs, annelids and flatworms but excludes the other protostome super-phylum Ecdysozoa, whose members include arthropods.{{sfn|Halanych: New phylogeny |(2004)}}{{cite journal|doi=10.1080/106351501753462830|last=de Rosa|first=R.|year=2001|title=Molecular Data Indicate the Protostome Affinity of Brachiopods|journal=Systematic Biology|volume=50|issue=6|pages=848–859|pmid=12116636|doi-access=free}} This conclusion is unanimous among molecular phylogeny studies that use a wide selection of genes: rDNA, Hox genes, mitochondrial protein genes, single nuclear protein genes and sets of nuclear protein genes.{{sfn|Helmkampf etc: Lophotrochozoa concept|(2008)}}

Some combined studies in 2000 and 2001, using both molecular and morphological data, support brachiopods as Lophotrochozoa,{{sfn|Giribet etc: Combined phylogeny|(2000)}}{{sfn|Peterson etc: Combined phylogeny|(2001)}} while others in 1998 and 2004 concluded that brachiopods were deuterostomes.{{sfn|Helmkampf etc: Lophotrochozoa concept|(2008)}}

The phoronids feed with a lophophore, burrow or encrust on surfaces, and build three-layered tubes made of polysaccharide, possibly chitin, mixed with particles with seabed material. Traditionally they have been regarded as a separate phylum, but increasingly detailed molecular phylogeny studies between 1997 and 2000 have concluded that phoronids are a sub-group of brachiopods.{{sfn|Cohen: Phoronids in Brachios|(2000|)}} However, an analysis in 2005 concluded that phoronids are a sub-group of bryozoans.{{sfn|Wood etc: Phylactolaemate Phylog|(2005)}}

While all molecular phylogeny studies and half the combined studies until 2008 conclude that brachiopods are lophotrochozoans, they could not identify which lophotrochozoan phylum were the closest relatives of brachiopods—except phoronids, which are a sub-group of brachiopods.{{sfn|Cohen: Phoronids in Brachios|(2000|)}}{{sfn|Helmkampf etc: Lophotrochozoa concept|(2008)}} However, in 2008 two analyses found that brachiopods' closest lophotrochozoan relatives were nemertines. The authors found this surprising, since nemertines have spiral cleavage in the early stages of cell division and form a trochophore larva, while brachiopods have radial cleavage and a larva that shows no sign of having evolved from a trochophore.{{sfn|Dunn etc: Close to Nemertines|(2008)}}{{sfn|Bourlat etc: Close to Nemertines|(2008)}} Another study in 2008 also concluded that brachiopods are closely related to nemertines, casting doubt on the idea that brachiopods are part of a clade Lophophorata of lophophore-feeding animals within the lophotrochozoans.{{sfn|Helmkampf etc: Lophotrochozoa concept|(2008)}}

File:Brachiopoda-morphology-en.svg|Brachiopod morphology

File:Cranaena.jpg|Cranaena, a terebratulid from the Middle Devonian of Wisconsin.

File:Brachiopod Neospirifer.jpg|The Carboniferous brachiopod Neospirifer condor from Bolivia. The specimen is 7 cm across.

File:Tylothyris.jpg|Tylothyris, a spiriferid from the Middle Devonian of Wisconsin

File:Rhynchotremadentatum.jpg|Rhynchotrema dentatum, a rhynchonellid brachiopod from the Cincinnatian (Upper Ordovician) of southeastern Indiana

File:HederellaOH3.jpg|A Devonian spiriferid brachiopod from Ohio that served as a host substrate for a colony of hederellids. The specimen is 5 cm wide.

File:Syringothyris texta Hall 1857 dorsal.jpg|Syringothyris texta (Hall 1857), dorsal view, internal mold. Lower Carboniferous of Wooster, Ohio

File:PetrocraniaOrdovician.jpg|Petrocrania brachiopods attached to a strophomenid brachiopod; Upper Ordovician of southeastern Indiana.

File:Lingula-Ozamis-1.JPG|Lingula found near Ozamiz City, Philippines

File:Barroisella.jpg|Barroisella, a lingulid from the Middle Devonian of Wisconsin.

File:Brachiopods Leberfinger quarry.jpg|Brachiopod casts in the Lock Haven Formation

File:HercosestriaSmallCluster040111.jpg|Hercosestria cribrosa Cooper & Grant 1969 (Roadian, Guadalupian, Middle Permian); Glass Mountains, Texas.

File:Productid interior ventral Permian Texas.JPG|Productid brachiopod ventral valve interior; Roadian, Guadalupian (Middle Permian); Glass Mountains, Texas.

File:Terebratella sanguinea.jpg|Terebratella sanguinea (Leach, 1814)

File:Schizophoria.jpg|Schizophoria, an orthid from the Middle Devonian of Wisconsin.

File:Striatochonetes.jpg|Striatochonetes, a chonetid from the Middle Devonian of Wisconsin.

File:Oleneothyris harlani (fossil brachiopod) (Tertiary; New Egypt, New Jersery, USA) 7.jpg|Oleneothyris, a terebratulid from the Cenozoic of New Jersey

File:Magellania joubini 01.jpg|A Magellania joubini from the Ross Sea

File:LoganBrachiopodsWooster.jpg|A mass burial of brachiopods from the Logan Formation (Mississippian) in Wooster, Ohio

File:Abyssothyris wyvillei - Brachiopods 01 (cropped).jpg|An Abyssothyris from the Challenger Plateau in the Pacific

File:Terebratalia transversa (brachiopod shell) (modern; offshore California, USA) 4.jpg|A Terebratalia transversa from California

• Taxonomy of the Brachiopoda
• Evolution of brachiopods
• List of brachiopod genera
• List of brachiopod species
• Novocrania anomala
• Margaret Jope

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{{Refend}}

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|journal= Palaeogeography, Palaeoclimatology, Palaeoecology

|year=2014

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|bibcode=2014PPP...411...42V }}

{{Commons category|Brachiopoda}}

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• [https://www.annualreviews.org/doi/pdf/10.1146/annurev-earth-060115-012348 The Evolution of Brachiopoda] – 2016 overview paper by [https://geology.ucdavis.edu/people/faculty/ Sandra J. Carlson], Department of Earth and Planetary Sciences, [https://www.ucdavis.edu/ University of Davis, California], at [https://www.annualreviews.org/ Annual Reviews] {{Webarchive|url=https://web.archive.org/web/20200423092945/https://www.annualreviews.org/ |date=2020-04-23 }}
• [http://paleopolis.rediris.es/BrachNet/ BrachNet]
• [http://paleopolis.rediris.es/brachiopoda_database/ Brachiopoda Database]
• [http://paleopolis.rediris.es/Brachiopoda_Phoronida_databases/ Brachiopoda World Database] - used from 1995 to 2015
• [https://web.archive.org/web/20080705173419/http://www.kgs.ku.edu/Extension/fossils/brachiopod.html Information from the Kansas Geological Survey]
• [http://perso.wanadoo.fr/jean-ours.filippi/brach/anglais/poursavoirplusang22.html Site of R.Filippi]
• [http://www.ucmp.berkeley.edu/brachiopoda/brachiopoda.html UC-Berkeley Museum of Paleontology]
• [https://web.archive.org/web/20060101163750/http://www.palaeos.com/Invertebrates/Lophotrochozoa/Brachiopoda/E0A0E0Brachiopoda.htm Palaeos Brachiopoda (last updated 2002)]
• [https://www.gutenberg.org/ebooks/73609 A Guide to the Shell and Starfish Galleries: (Mollusca, Polyzoa, Brachiopoda, Tunicata, Echinoderma, and Worms)] (1901), British Museum (Natural History). Department of Zoology et al.

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Category:Extant Cambrian first appearances

Category:Taxa named by André Marie Constant Duméril