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Siboglinidae

Siboglinidae is a family of polychaete annelid worms whose members made up the former phyla Pogonophora and Vestimentifera. The family is composed of around 100 species of vermiform creatures which live in thin tubes buried in sediment (Pogonophora) or in tubes attached to hard substratum (Vestimentifera) at ocean depths ranging from 100 to 10,000 m. They can also be found in association with hydrothermal vents, methane seeps, sunken plant material, and whale carcasses.

Anatomy
Most siboglinids are less than in diameter, but in length. They inhabit tubular structures composed of chitin which are fixed to rocks or other substrates. The tubes are often clustered together in large colonies. The body cavity has a separate compartment in each of the first three regions of the body and extends into the tentacles. The opisthosoma has a coelomic chamber in each of its 5 to 23 segments, separated by septa. The worms have a complex closed circulatory system and a well-developed nervous system, but as adults, siboglinids completely lack a mouth, gut, and anus. Their bodies are divided into four regions. The anterior end is called the cephalic lobe, which ranges from one to over 200 thin branchial ciliated tentacles, each with tiny side branches known as pinnules. Behind this is a glandular forepart, which helps to secrete the tube. The main part of the body is the trunk, which is greatly elongated and bears various annuli, papillae, and ciliary tracts. Posterior to the trunk is the short metamerically segmented opisthosoma, bearing external paired chaetae, which help to anchor the animal to the base of its tube. ==Evolution==
Evolution
}} }} The family Siboglinidae has been difficult to place in an evolutionary context. After examination of genetic differences between annelids, Siboglinidae were placed within the order Polychaeta by scientific consensus. The fossil record along with molecular clocks suggest the family has Mesozoic (250 – 66 Mya) or Cenozoic (66 Mya – recent) origins. These tubes, known as 'Figueroa tubes', along the 'Troodos collared tubes' (Cyprus, Turonian) were resolved among modern vestimentiferans. Molecular work aligning five genes has identified four distinct clades within Siboglinidae, These being Vestimentifera, Sclerolinum, Frenulata, and Osedax. Sclerolinum is a monogeneric clade (which may be called Monilifera) living on organic-rich remains. Osedax is a monogeneric clade specialized in living on whale bones, although recent evidence shows them living on fish bones as well. The following are cladograms of Siboglinidae: }} }} }} ==Genera==
Genera
• Clade FrenulataChoanophorusCrassibrachiaCyclobrachiaDiplobrachiaGalathealinumHeptabrachiaLamellisabellaNereilinumOligobrachiaParaescarpiaPolybrachiaSiboglinoidesSiboglinumSiphonobrachiaSpirobrachiaUnibrachiumVolvobrachiaZenkevitchiana • Clade MoniliferaSclerolinum • Clade VestimentiferaAlaysiaArcovesiaEscarpiaLamellibrachiaOasisiaRidgeiaRiftiaTevniaincertae sedisOsedax ==Vestimentiferans==
Vestimentiferans
Like other tube worms, vestimentiferans are benthic marine creatures. Riftia pachyptila, a vestimentiferan, is known only from the hydrothermal vent systems. }} Anatomy of vestimentiferans '' removed from its tube: op = opisthosome, ves = vestimentum, ten = tentacular region, tr = trunk Vestimentiferan bodies are divided into four regions: the obturaculum, vestimentum, trunk, and opisthosome. The main trunk of the body bears wing-like extensions. Unlike other siboglinids that never have a digestive tract, they have one that they completely lose during metamorphosis. The obturaculum is the first anterior body part. It is possible that the obturaculum is actually an outgrowth of the vestimentum rather than a separate body segment which would distinguish it from other siboglinids. The vestimentum, from which the group's name is derived, is a wing-like body part with glands that secrete the tube. In a ventroanterior position in the vestimentum is the brain which is postulated to be simpler than relatives that maintain a gut in the adult form. This method of entry, known as horizontal transmission, means that each organism may have different species of bacteria assisting in this symbiosis. However, these bacteria all play similar roles in sustaining the vestimentiferans. Endosymbionts have a wide variety of metabolic genes, which may allow them to switch between autotrophic and heterotrophic methods of nutrient acquisition. When the host dies, the bacteria are released and return to the free-living population in the seawater. Discovery of the hydrothermal vents in the eastern Pacific Ocean was quickly followed by the discovery and description of new vestimentiferan tubeworm species. These tubeworms are one of the most dominant organisms associated with the hydrothermal vents in the Pacific Ocean. Tubeworms anchor themselves to the substratum of the hydrocarbon seep by roots located at the basal portion of their bodies. Intact tubeworm roots have proven very difficult to obtain for study because they are extremely delicate, and often break off when a tubeworm is removed from hypothermal vent regions. How long the roots of the tube worms can grow is unknown, but roots have been recovered longer than 30 m. A single aggregation of tubeworms can contain thousands of individuals, and the roots produced by each tubeworm can become tangled with the roots of neighbouring tubeworms. These mats of roots are known as "ropes", and travel down the tubes of dead tubeworms, and run through holes in rocks. The diameter and wall thickness of the tubeworm roots do not appear to change with distance from the trunk portion of the tubeworm's body. Like the trunk portion of the body, the roots of the vestimentiferan tubeworms are composed of chitin crystallites, which support and protect the tubeworm from predation and environmental stresses. Tubeworms build the external chitin structure themselves by secreting chitin from specialized glands located in their body walls. ==References==
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