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Sponges or sea sponges are primarily marine invertebrates of the animal phylum Porifera. They are sessile filter feeders that are bound to the seabed, and are one of the most ancient members of macrobenthos, with many historical species being important reef-building organisms.

Etymology
The term sponge derives from the Ancient Greek word . The scientific name Porifera is a neuter plural of the Modern Latin term porifer, which comes from the roots porus meaning "pore, opening", and -fer meaning "bearing or carrying". == Overview ==
Overview
Sponges are similar to other animals in that they are multicellular heterotrophs that lack cell walls and produce sperm cells. Unlike other animals, they lack true tissues and organs. Some of them are radially symmetrical, but most are asymmetrical. The shapes of their bodies are adapted for maximal efficiency of water flow through the central cavity, where the water deposits nutrients and then leaves through a hole called the osculum. Their choanocyte cells are used to drive their water flow systems and capture most of their food. This, along with phylogenetic studies of ribosomal molecules, has been used as morphological evidence to suggest sponges are the sister group to the rest of animals. A great majority are marine (salt-water) species, ranging in habitat from tidal zones to depths exceeding , though the freshwater sponges inhabit all continents other than Antarctica. All adult sponges are sessile, meaning that they attach to an underwater surface and remain fixed in place (i.e., do not travel). While in their larval stage of life, they are motile. Many sponges have a mesh-like endoskeleton composed of spicules made of either calcium carbonate or silicon dioxide (silica), embedded within spongin (a modified type of collagen). Most sponges reproduce sexually, but they can also reproduce asexually. Sexually reproducing species release sperm cells into the water to fertilize ova released or retained by its mate or "mother"; the fertilized eggs develop into larvae which swim off in search of places to settle. Sponges are known for regenerating from fragments that are broken off, although this only works if the fragments include the right types of cells. Some species reproduce by budding. When environmental conditions become less hospitable to the sponges, for example as temperatures drop, many freshwater species and a few marine ones produce gemmules, "survival pods" of unspecialized cells that remain dormant until conditions improve; they then either form completely new sponges or recolonize the skeletons of their parents. The few species of demosponge that have entirely soft fibrous skeletons with no hard elements have been used by humans over thousands of years for several purposes, including as padding and as cleaning tools. By the 1950s, though, these had been overfished so heavily that the industry almost collapsed, and most sponge-like materials are now synthetic. Sponges and their microscopic endosymbionts are now being researched as possible sources of medicines for treating a wide range of diseases. Dolphins have been observed using sponges as tools while foraging. == Distinguishing features ==
Distinguishing features
Sponges constitute the phylum Porifera, and have been defined as sessile metazoans (multicelled immobile animals) that have water intake and outlet openings connected by chambers lined with choanocytes, cells with whip-like flagella. All known living sponges can remold their bodies, as most types of their cells can move within their bodies and a few can change from one type to another. Even if a few sponges are able to produce mucus – which acts as a microbial barrier in all other animals – no sponge with the ability to secrete a functional mucus layer has been recorded. Without such a mucus layer their living tissue is covered by a layer of microbial symbionts, which can contribute up to 40–50% of the sponge wet mass. This inability to prevent microbes from penetrating their porous tissue could be a major reason why they have never evolved a more complex anatomy. Like cnidarians (jellyfish, etc.) and ctenophores (comb jellies), and unlike all other known metazoans, sponges' bodies consist of a non-living jelly-like mass (mesohyl) sandwiched between two main layers of cells. Cnidarians and ctenophores have simple nervous systems, and their cell layers are bound by internal connections and by being mounted on a basement membrane a thin fibrous mat, also known as a basal lamina. Sponges do not have a nervous system similar to that of vertebrates but may have one that is quite different. Their middle jelly-like layers have large and varied populations of cells, and some types of cells in their outer layers may move into the middle layer and change their functions. == Basic structure ==
Basic structure
Cell types A sponge's body is hollow and is held in shape by the mesohyl, a jelly-like substance made mainly of collagen and reinforced by a dense network of fibers also made of collagen. 18 distinct cell types have been identified. The inner surface is covered with choanocytes, cells with cylindrical or conical collars surrounding one flagellum per choanocyte. The wave-like motion of the whip-like flagella drives water through the sponge's body. All sponges have ostia, channels leading to the interior through the mesohyl, and in most sponges these are controlled by tube-like porocytes that form closable inlet valves. Pinacocytes, plate-like cells, form a single-layered external skin over all other parts of the mesohyl that are not covered by choanocytes, and the pinacocytes also digest food particles that are too large to enter the ostia, Glass sponges present a distinctive variation on this basic plan. Their spicules, which are made of silica, form a scaffolding-like framework between whose rods the living tissue is suspended like a cobweb that contains most of the cell types. or calcium carbonate, and vary in shape from simple rods to three-dimensional "stars" with up to six rays. Spicules are produced by sclerocyte cells, and may be separate, connected by joints, or fused. Some sponges also secrete exoskeletons that lie completely outside their organic components. For example, sclerosponges ("hard sponges") have massive calcium carbonate exoskeletons over which the organic matter forms a thin layer with choanocyte chambers in pits in the mineral. These exoskeletons are secreted by the pinacocytes that form the animals' skins. == Vital functions ==
Vital functions
'', "the kitchen sponge", is dark grey when alive. Movement Although adult sponges are fundamentally sessile animals, some marine and freshwater species can move across the sea bed at speeds of per day, as a result of amoeba-like movements of pinacocytes and other cells. A few species can contract their whole bodies, and many can close their oscula and ostia. Juveniles drift or swim freely, while adults are stationary. Archaeocytes transport food packaged in vesicles from cells that directly digest food to those that do not. At least one species of sponge has internal fibers that function as tracks for use by nutrient-carrying archaeocytes, However, a study in 2007 found no evidence of this and concluded that they extract bacteria and other micro-organisms from water very efficiently (about 79%) and process suspended sediment grains to extract such prey. Collar bodies digest food and distribute it wrapped in vesicles that are transported by dynein "motor" molecules along bundles of microtubules that run throughout the syncytium. In waters where the supply of food particles is very poor, some species prey on crustaceans and other small animals. , a total of 137 species had been discovered. Most belong to the family Cladorhizidae, but a few members of the Guitarridae and Esperiopsidae are also carnivores. Most carnivorous sponges live in deep waters, up to , and the development of deep-ocean exploration techniques is expected to lead to the discovery of several more. However, Lycopodina hypogea has been found in relatively shallow depths of in Mediterranean sea caves. These cave-dwelling predators capture prey using filaments equipped with hooked spicules, and digest them by enveloping them with more threads over the course of a few days. Endosymbionts Freshwater sponges often host green algae as endosymbionts within archaeocytes and other cells and benefit from nutrients produced by the algae. Many marine species host other photosynthesizing organisms, most commonly cyanobacteria but in some cases dinoflagellates. Symbiotic cyanobacteria may form a third of the total mass of living tissue in some sponges, and some sponges gain 48% to 80% of their energy supply from these micro-organisms. Sponges that host photosynthesizing organisms are most common in waters with relatively poor supplies of food particles and often have leafy shapes that maximize the amount of sunlight they collect. The different sponge classes regenerate using distinct methods. but they are able to regenerate even from dissociated cells; after being subjected to chemical or mechanical tissue destruction, these dissociated cells reaggregate to begin the process of regeneration, and after reforming the epithelium, gradually reconstruct their anatomy, such as the water circulation system. This "whole-body regeneration" has been observed in demosponges, calcareous sponges, and homoscleromorphs. Cell death appears to have a limited role in whole-body regeneration, mainly occurring while the epithelium reforms. Glass sponges are also able to regenerate; Rhabdocalyptus dawsoni is able to regenerate at a rate of per day, filling in from the atrial, then dermal side, and closing up to form a scar. This rate is up to 40 times faster than growth of new tissue in the species, which may be due to the cytoplasmic method glass sponges use, as opposed to the slower cellular method in other sponges. Regeneration is noted to be faster than normal growth, as seen in Aplysilla rosea. Additionally, regeneration at the base appears to occur faster than that occurring at the apex (top) of the sponge, at least in Cinachyrella cf. cavernosa. Reproduction Asexual Spongilla lacustris Sponges have three asexual methods of reproduction: after fragmentation, by budding, and by producing gemmules. Fragments of sponges may be detached by currents or waves. They use the mobility of their pinacocytes and choanocytes and reshaping of the mesohyl to re-attach themselves to a suitable surface and then rebuild themselves as small but functional sponges over the course of several days. The same capabilities enable sponges that have been squeezed through a fine cloth to regenerate. The gemmules then become dormant, and in this state can survive cold, drying out, lack of oxygen and extreme variations in salinity. There are four types of larvae, but all are lecithotrophic (non-feeding) balls of cells with an outer layer of cells whose flagella or cilia enable the larvae to move. After swimming for a few days the larvae sink and crawl until they find a place to settle. Most of the cells transform into archeocytes and then into the types appropriate for their locations in a miniature adult sponge. Glass sponge embryos start by dividing into separate cells, but once 32 cells have formed they rapidly transform into larvae that externally are ovoid with a band of cilia round the middle that they use for movement, but internally have the typical glass sponge structure of spicules with a cobweb-like main syncitium draped around and between them and choanosyncytia with multiple collar bodies in the center. The larvae then leave their parents' bodies. Meiosis The cytological progression of porifera oogenesis and spermatogenesis (gametogenesis) is very similar to that of other metazoa. Most of the genes from the classic set of meiotic genes, including genes for DNA recombination and double-strand break repair, that are conserved in eukaryotes are expressed in the sponges (e.g. Geodia hentscheli and Geodia phlegraei). Demosponge Samus anonymus (up to 50 m), hexactinellid Scleroplegma lanterna (~100–600 m), hexactinellid Aulocalyx irregularis (~550–915 m), lithistid demosponge Neoaulaxinia persicum (~500–1700 m) Sponges in temperate regions live for at most a few years, but some tropical species and perhaps some deep-ocean ones may live for 200 years or more. Some calcified demosponges grow by only per year and, if that rate is constant, specimens wide must be about 5,000 years old. Some sponges start sexual reproduction when only a few weeks old, while others wait until they are several years old. However, glass sponges rapidly transmit electrical impulses through all parts of the syncytium, and use this to halt the motion of their flagella if the incoming water contains toxins or excessive sediment. == Ecology ==
Ecology
Habitats '' is a deep ocean glass sponge, seen here at a depth of off the coast of California Sponges are worldwide in their distribution, living in a wide range of ocean habitats, from the polar regions to the tropics. Sponges are more abundant but less diverse in temperate waters than in tropical waters, possibly because organisms that prey on sponges are more abundant in tropical waters. Glass sponges are the most common in polar waters and in the depths of temperate and tropical seas, as their very porous construction enables them to extract food from these resource-poor waters with the minimum of effort. Demosponges and calcareous sponges are abundant and diverse in shallower non-polar waters. The different classes of sponge live in different ranges of habitat: : As primary producers Sponges with photosynthesizing endosymbionts produce up to three times more oxygen than they consume, as well as more organic matter than they consume. Such contributions to their habitats' resources are significant along Australia's Great Barrier Reef but relatively minor in the Caribbean. and another study found that high levels of coral predation did predict the presence of chemically defended species. Glass sponges produce no toxic chemicals, and live in very deep water where predators are rare. Spongeflies, also known as spongillaflies (Neuroptera, Sisyridae), are specialist predators of freshwater sponges. The female lays her eggs on vegetation overhanging water. The larvae hatch and drop into the water where they seek out sponges to feed on. They use their elongated mouthparts to pierce the sponge and suck the fluids within. The larvae of some species cling to the surface of the sponge while others take refuge in the sponge's internal cavities. The fully grown larvae leave the water and spin a cocoon in which to pupate. Bioerosion The Caribbean chicken-liver sponge Chondrilla nucula secretes toxins that kill coral polyps, allowing the sponges to grow over the coral skeletons. The rust-colored bands are caused by a cyanobacterium, but it is unknown whether this organism actually causes the disease. Collaboration with other organisms In addition to hosting photosynthesizing endosymbionts, Shrimps of the genus Synalpheus form colonies in sponges, and each shrimp species inhabits a different sponge species, making Synalpheus one of the most diverse crustacean genera. Specifically, Synalpheus regalis utilizes the sponge not only as a food source, but also as a defense against other shrimp and predators. As many as 16,000 individuals inhabit a single loggerhead sponge, feeding off the larger particles that collect on the sponge as it filters the ocean to feed itself. Other crustaceans such as hermit crabs commonly have a specific species of sponge, Pseudospongosorites, grow on them as both the sponge and crab occupy gastropod shells until the crab and sponge outgrow the shell, eventually resulting in the crab using the sponge's body as protection instead of the shell until the crab finds a suitable replacement shell. Sponge loop (DOM), (2) sponges take up DOM, (3) sponges release detrital particulate organic matter (POM), (4) sponge detritus (POM) is taken up by sponge-associated and free-living detritivores. Most sponges are detritivores which filter organic debris particles and microscopic life forms from ocean water. In particular, sponges occupy an important role as detritivores in coral reef food webs by recycling detritus to higher trophic levels. and transfer organic matter produced by corals further up the reef food web. Corals release organic matter as both dissolved and particulate mucus, as well as cellular material such as expelled Symbiodinium. Coral-derived organic matter could also be indirectly transferred to sponges via bacteria, which can also consume coral mucus. Besides a one to one symbiotic relationship, it is possible for a host to become symbiotic with a microbial consortium, resulting in a diverse sponge microbiome. Sponges are able to host a wide range of microbial communities that can also be very specific. The microbial communities that form a symbiotic relationship with the sponge can amount to as much as 35% of the biomass of its host. The term for this specific symbiotic relationship, where a microbial consortia pairs with a host is called a holobiotic relationship. The sponge as well as the microbial community associated with it will produce a large range of secondary metabolites that help protect it against predators through mechanisms such as chemical defense. The sponge holobiont is an example of the concept of nested ecosystems. Environmental factors act at multiple scales to alter microbiome, holobiont, community, and ecosystem scale processes. Thus, factors that alter microbiome functioning can lead to changes at the holobiont, community, or even ecosystem level and vice versa, illustrating the necessity of considering multiple scales when evaluating functioning in nested ecosystems. Some of these relationships include endosymbionts within bacteriocyte cells, and cyanobacteria or microalgae found below the pinacoderm cell layer where they are able to receive the highest amount of light, used for phototrophy. They can host over 50 different microbial phyla and candidate phyla, including Alphaprotoebacteria, Actinomycetota, Chloroflexota, Nitrospirota, "Cyanobacteria", the taxa Gamma-, the candidate phylum Poribacteria, and Thaumarchaea. == Systematics ==
Systematics
Taxonomy Carl Linnaeus, who classified most kinds of sessile animals as belonging to the order Zoophyta in the class Vermes, mistakenly identified the genus Spongia as plants in the order Algae. For a long time thereafter, sponges were assigned to subkingdom Parazoa ("beside the animals") separated from the Eumetazoa which formed the rest of the kingdom Animalia. However, in the 1980s, it was found that these were all members of either the Calcarea or the Demospongiae. So far scientific publications have identified about 9,000 poriferan species, Sponges are divided into classes mainly according to the composition of their skeletons: Additionally, the monophyly of the phylum is now under question. Several studies have concluded that all other animals emerged from within the sponges, and usually recover that the calcareous sponges and Homoscleromorpha are closer to other animals than to demosponges. The internal relationships of Porifera have proven to be less uncertain. A close relationship of Homoscleromorpha and Calcarea has been recovered in nearly all studies, whether or not they support sponge or eumetazoan monophyly. The position of glass sponges is also fairly certain, with a majority of studies recovering them as the sister of the demosponges. Thus, the uncertainty at the base of the animal family tree is probably best represented by the below cladogram. }} == Evolutionary history ==
Evolutionary history
Fossil record '', a fossil sponge from the Cretaceous of England '', a fossil anthaspidellid demosponge from the early Ordovician of Nevada Although molecular clocks and biomarkers suggest sponges existed well before the Cambrian explosion of life, silica spicules like those of demosponges are absent from the fossil record until the Cambrian. An unsubstantiated 2002 report exists of spicules in rocks dated around . Well-preserved fossil sponges from about in the Ediacaran period have been found in the Doushantuo Formation. These fossils, which include: spicules; pinacocytes; porocytes; archeocytes; sclerocytes; and the internal cavity, have been classified as demosponges. The Ediacaran record of sponges also contains two other genera: the stem-hexactinellid Helicolocellus from the Dengying Formation and the possible stem-archaeocyathan Arimasia from the Nama Group. These genera are both from the "Nama assemblage" of Ediacaran biota, although whether this is due to a genuine lack beforehand or preservational bias is uncertain. Fossils of glass sponges have been found from around in rocks in Australia, China, and Mongolia. Early Cambrian sponges from Mexico belonging to the genus Kiwetinokia show evidence of fusion of several smaller spicules to form a single large spicule. Calcium carbonate spicules of calcareous sponges have been found in Early Cambrian rocks from about in Australia. Other probable demosponges have been found in the Early Cambrian Chengjiang fauna, from . Fossils found in the Canadian Northwest Territories dating to may be sponges; if this finding is confirmed, it suggests the first animals appeared before the Neoproterozoic oxygenation event. Freshwater sponges appear to be much younger, as the earliest known fossils date from the Mid-Eocene period about . The earliest sponge symbionts are known from the early Silurian. A chemical tracer is 24-isopropyl cholestane, which is a stable derivative of 24-isopropyl cholesterol, which is said to be produced by demosponges but not by eumetazoans ("true animals", i.e. cnidarians and bilaterians). Since choanoflagellates are thought to be animals' closest single-celled relatives, a team of scientists examined the biochemistry and genes of one choanoflagellate species. They concluded that this species could not produce 24-isopropyl cholesterol but that investigation of a wider range of choanoflagellates would be necessary in order to prove that the fossil 24-isopropyl cholestane could only have been produced by demosponges. Although a previous publication reported traces of the chemical 24-isopropyl cholestane in ancient rocks dating to , recent research using a much more accurately dated rock series has revealed that these biomarkers only appear before the end of the Marinoan glaciation approximately , and that "Biomarker analysis has yet to reveal any convincing evidence for ancient sponges pre-dating the first globally extensive Neoproterozoic glacial episode (the Sturtian, ~ in Oman)". While it has been argued that this 'sponge biomarker' could have originated from marine algae, recent research suggests that the algae's ability to produce this biomarker evolved only in the Carboniferous; as such, the biomarker remains strongly supportive of the presence of demosponges in the Cryogenian. Archaeocyathids, which some classify as a type of coralline sponge, are very common fossils in rocks from the Early Cambrian about , but apparently died out by the end of the Cambrian . It is difficult to fit chancelloriids into classifications of sponges or more complex animals. An analysis in 1996 concluded that they were closely related to sponges on the grounds that the detailed structure of chancellorid sclerites ("armor plates") is similar to that of fibers of spongin, a collagen protein, in modern keratose (horny) demosponges such as Darwinella. However, another analysis in 2002 concluded that chancelloriids are not sponges and may be intermediate between sponges and more complex animals, among other reasons because their skins were thicker and more tightly connected than those of sponges. In 2008, a detailed analysis of chancelloriids' sclerites concluded that they were very similar to those of halkieriids, mobile bilaterian animals that looked like slugs in chain mail and whose fossils are found in rocks from the very Early Cambrian to the Mid Cambrian. If this is correct, it would create a dilemma, as it is extremely unlikely that totally unrelated organisms could have developed such similar sclerites independently, but the huge difference in the structures of their bodies makes it hard to see how they could be closely related. Relationships to other animal group In the 1990s, sponges were widely regarded as a monophyletic group, all of them having descended from a common ancestor that was itself a sponge, and as the "sister-group" to all other metazoans (multi-celled animals), which themselves form a monophyletic group. On the other hand, some 1990s analyses also revived the idea that animals' nearest evolutionary relatives are choanoflagellates, single-celled organisms very similar to sponges' choanocytes – which would imply that most Metazoa evolved from very sponge-like ancestors and therefore that sponges may not be monophyletic, as the same sponge-like ancestors may have given rise both to modern sponges and to non-sponge members of Metazoa. Analyses since 2001 have concluded that Eumetazoa (more complex than sponges) are more closely related to particular groups of sponges than to other sponge groups. Such conclusions imply that sponges are not monophyletic, because the last common ancestor of all sponges would also be a direct ancestor of the Eumetazoa, which are not sponges. A study in 2001 based on comparisons of ribosome DNA concluded that the most fundamental division within sponges was between glass sponges and the rest, and that Eumetazoa are more closely related to calcareous sponges (those with calcium carbonate spicules) than to other types of sponge. Other anatomical and biochemical evidence links the Eumetazoa with Homoscleromorpha, a sub-group of demosponges. A comparison in 2007 of nuclear DNA, excluding glass sponges and comb jellies, concluded that: • Homoscleromorpha are most closely related to Eumetazoa; • calcareous sponges are the next closest; • the other demosponges are evolutionary "aunts" of these groups; and • the chancelloriids, bag-like animals whose fossils are found in Cambrian rocks, may be sponges. The sperm of Homoscleromorpha share features with the sperm of Eumetazoa, that sperm of other sponges lack. In both Homoscleromorpha and Eumetazoa layers of cells are bound together by attachment to a carpet-like basal membrane composed mainly of "typ IV" collagen, a form of collagen not found in other sponges – although the spongin fibers that reinforce the mesohyl of all demosponges is similar to "type IV" collagen. The analyses described above concluded that sponges are closest to the ancestors of all Metazoa, of all multi-celled animals including both sponges and more complex groups. However, another comparison in 2008 of 150 genes in each of 21 genera, ranging from fungi to humans but including only two species of sponge, suggested that comb jellies (ctenophora) are the sister group to all other lineages of Metazoa included in the sample. If this is correct, either modern comb jellies developed their complex structures independently of other Metazoa, or sponges' ancestors were more complex and all known sponges are drastically simplified forms. The study recommended further analyses using a wider range of sponges and other simple Metazoa such as Placozoa. 'Family trees' constructed using a combination of all available data – morphological, developmental and molecular – concluded that the sponges are in fact a monophyletic group, and with the cnidarians form the sister group to the bilaterians. A very large and internally consistent alignment of 1,719 proteins at the metazoan scale, published in 2017, showed that (i) sponges – represented by Homoscleromorpha, Calcarea, Hexactinellida, and Demospongiae – are monophyletic, (ii) sponges are sister-group to all other multicellular animals, (iii) ctenophores emerge as the second-earliest branching animal lineage, and (iv) placozoans emerge as the third animal lineage, followed by cnidarians sister-group to bilaterians. In March 2021, scientists from Dublin found additional evidence that sponges are the sister group to all other animals, while in May 2023, Schultz et al. found patterns of irreversible change in genome synteny that provide strong evidence that ctenophores are the sister group to all other animals instead. == Notable spongiologists ==
Use
By dolphins A report in 1997 described use of sponges as a tool by bottlenose dolphins in Shark Bay in Western Australia. A dolphin will attach a marine sponge to its rostrum, which is presumably then used to protect it when searching for food in the sandy sea bottom. The behavior, known as sponging, has only been observed in this bay and is almost exclusively shown by females. A study in 2005 concluded that mothers teach the behavior to their daughters and that all the sponge users are closely related, suggesting that it is a fairly recent innovation. By humans Skeleton The calcium carbonate or silica spicules of most sponge genera make them too rough for most uses, but two genera, Hippospongia and Spongia, have soft, entirely fibrous skeletons. Many objects with sponge-like textures are now made of substances not derived from poriferans. Synthetic sponges include personal and household cleaning tools, breast implants, and contraceptive sponges. Typical materials used are cellulose foam, polyurethane foam, and less frequently, silicone foam. The luffa "sponge", also spelled loofah, which is commonly sold for use in the kitchen or the shower, is not derived from an animal but mainly from the fibrous "skeleton" of the sponge gourd (Luffa aegyptiaca, Cucurbitaceae). File:2008.09-331-196ap Sponge gourd,pd Spice Bazaar@Istanbul,TR mon29sep2008-1315h.jpg|Sponges made of sponge gourd for sale alongside sponges of animal origin, Spice Bazaar, Istanbul File:SpongesTarponSprings.jpg|Natural sponges in Tarpon Springs, Florida Medicinal compounds precursor halichondrin B Sponges have medicinal potential due to the presence in sponges themselves or their microbial symbionts of chemicals that may be used to control viruses, bacteria, tumors and fungi. Lacking any protective shell or means of escape, sponges have evolved to synthesize a variety of unusual compounds. One such class is the oxidized fatty acid derivatives called oxylipins. Members of this family have been found to have anti-cancer, anti-bacterial and anti-fungal properties. One example isolated from the Okinawan Plakortis sponges, plakoridine A, has shown potential as a cytotoxin to murine lymphoma cells. == See also ==
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