Fossil range: Ediacaran–Recent
Sponges are animals of the phylum Porifera (pronounced /pɒˈrɪfərə/). Their bodies consist of jelly-like mesohyl sandwiched between two thin layers of cells. While all animals have unspecialized cells that can transform into specialized cells, sponges are unique in having some specialized cells that can transform into other types, often migrating between the main cell layers and the mesohyl in the process. Sponges do not have nervous, digestive or circulatory systems. Instead, most rely on maintaining a constant water flow through their bodies to obtain food and oxygen and to remove wastes, and the shapes of their bodies are adapted to maximize the efficiency of the water flow. All are sessile aquatic animals and, although there are freshwater species, the great majority are marine (salt water) species, ranging from tidal zones to depths exceeding 8,800 metres (5.5 mi). While most of the approximately 5,000-10,000 known species feed on bacteria and other food particles in the water, some host photosynthesizing micro-organisms as endosymbionts and these alliances often produce more food and oxygen than they consume. A few species of sponge that live in food-poor environments have become carnivores that prey mainly on small crustaceans.
Sponges are known for regenerating from fragments that are broken off, although this only works if the fragments include the right types of cells. A few species reproduce by budding. When conditions deteriorate, 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 and then either form completely new sponges or re-colonize the skeletons of their parents.
However most sponges use sexual reproduction, releasing sperm cells into the water. In viviparous species the cells that capture most of the adults' food capture the sperm cells but, instead of digesting them, transport them to ova in the parent's mesohyl. The fertilized eggs begin development within the parent and the larvae are released to swim off in search of places to settle. In oviparous species both sperm and egg cells are released into the water and fertilisation and development take place outside the parent's bodies.
Sponges use various materials to reinforce their mesohyl and in some cases to produce skeletons, and this forms the main basis for classifying sponges. Calcareous sponges produce spicules made of calcium carbonate. Demosponges reinforce the mesohyl with fibers of a special form of collagen called spongin, most also produce spicules of silica, and a few secrete massive external frameworks of calcium carbonate. Although glass sponges also produce spicules made of silica, their bodies mainly consist of syncytia that in some ways behave like many cells sharing a single external membrane, and in others like individual cells with multiple nuclei. Probably because of their variety of construction methods, demosponges constitute about 90% of all known species, including all freshwater ones, and have the widest range of habitats. Calcareous sponges are restricted to relatively shallow marine waters where production of calcium carbonate is easiest. The fragile glass sponges are restricted to polar regions and the ocean depths where predators are rare, and their feeding systems very efficiently harvest what little food is available. Fossils of all of these types have been found in rocks dated from . In addition Archaeocyathids, whose fossils are common in rocks from but not after , are now regarded as a type of sponge.
It is generally thought that sponges' closest single-celled relatives are choanoflagellates, which strongly resemble the cells that sponges use to drive their water flow systems and capture most of their food. It is also generally agreed that sponges do not form a monophyletic group, in other words do not include all and only the descendants of a common ancestor, because it is thought that Eumetazoa (more complex animals) are descendants of a sub-group of sponges. However it is uncertain which group of sponges is closest to Eumetazoa, as both calcareous sponges and a sub-group of demosponges called Homoscleromorpha have been nominated by different researchers. In addition a study in 2008 suggested that the earliest animals may have been similar to modern comb jellies. Since comb jellies are considerably more complex than sponges, this would imply that sponges had mobile ancestors and greatly simplified their bodies as they adapted to a sessile filter feeding lifestyle. Chancelloriids, sessile, bag-like organisms whose fossils are found only in rocks from the Cambrian period, increase the uncertainty as it has been suggested that they were sponges but also that their external spines resemble the "chain mail" of the slug-like Halkieriids.
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. However by the 1950s these had been over-fished 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.
Sponges constitute the phylum Porifera, and have been defined as sessile metazoans (multi-celled animals) that have water intake and outlet openings connected by chambers lined with choanocytes, cells with whip-like flagella. However, a few carnivorous sponges have lost these water flow systems and the choanocytes. 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.
Like cnidarians (jellyfish, etc.) and ctenophores (comb jellies), and unlike all other known metazoans, sponges' bodies consist of a non-living jelly-like mass 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 (thin fibrous mat, also known as "basal lamina"). Sponges have no nervous systems, their middle jelly-like layers have large and varied populations of cells, and some types of cell in their outer layers may move into the middle layer and change their functions.
|Sponges||Cnidarians and ctenophores|
|Nervous system||No||Yes, simple|
|Cells in each layer bound together||No , except that Homoscleromorpha have basement membranes.||Yes: inter-cell connections; basement membranes|
|Number of cells in middle "jelly" layer||Many||Few|
|Cells in outer layers can move inwards and change functions||Yes||No|
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. 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 skin over all other parts of the mesohyl that are not covered by choanocytes, and the external pinacocytes also digest food particles that are too large to enter the ostia, while those at the base of the animal are responsible for anchoring it.
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. This tissue is a syncytium that in some ways behaves like many cells that share a single external membrane, and in others like a single cell with multiple nuclei. The mesohyl is absent or minimal. The syncytium's cytoplasm, the soupy fluid that fills the interiors of cells, is organised into "rivers" that transport nuclei, organelles ("organs" within cells) and other substances. Instead of choanocytes they have further syncytia, known as choanosyncytia, which form bell-shaped chambers which water enters via perforations. The insides of these chambers are lined with "collar bodies", each consisting of a collar and flagellum but without a nucleus of its own. The motion of the flagella sucks water through passages in the "cobweb" and expels it via the open ends of the bell-shaped chambers.
Some types of cells have a single nucleus and membrane each, but are connected to other single-nucleus cells and to the main syncytium by "bridges" made of cytoplasm. The sclerocytes that build spicules have multiple nuclei, and in glass sponge larvae they are connected to other tissues by cytoplasm bridges; such connections between sclerocytes have not so far been found in adults, but this may simply reflect the difficulty of investigating such small-scale features. The bridges are controlled by "plugged junctions" that apparently permit some substances to pass while blocking others.
Most sponges work rather like chimneys: they take in water at the bottom and eject it from the osculum ("little mouth") at the top. Since ambient currents are faster at the top, the suction effect that they produce does some of the work for free. Sponges can control the water flow by various combinations of wholly or partially closing the osculum and ostia (the intake pores) and varying the beat of the flagella, and may shut it down if there is a lot of sand or silt in the water.
Although the layers of pinacocytes and choanocytes resemble the epithelia of more complex animals, they are not bound tightly by cell-to-cell connections or a basal lamina (thin fibrous sheet underneath). The flexibility of these layers and re-modeling of the mesohyl by lophocytes allow the animals to adjust their shapes throughout their lives to take maximum advantage of local water currents.
The simplest body structure in sponges is a tube or vase shape known as "asconoid", but this severely limits the size of the animal. If it is simply scaled up, the ratio of its volume to surface area increases, because surface increases as the square of length or width while volume increases proportionally to the cube. The amount of tissue that needs food and oxygen is determined by the volume, but the pumping capacity that supplies food and oxygen depends on the area covered by choanocytes. Asconoid sponges seldom exceed 1 millimetre (0.039 in) in diameter.
Some sponges overcome this limitation by adopting the "syconoid" structure, in which the body wall is pleated. The inner pockets of the pleats are lined with choanocytes, which connect to the outer pockets of the pleats by ostia. This increase in the number of choanocytes and hence in pumping capacity enables syconoid sponges to grow up to a few centimeters in diameter. The "leuconid" pattern boosts pumping capacity further by filling the interior almost completely with mesohyl that contains a network of chambers lined with choanocytes and connected to each other and to the water intakes and outlet by tubes. Leuconid sponges grow to over 1 metre (3.3 ft) in diameter, and the fact that growth in any direction increases the number of choanocyte chambers enables them to take a wider range of forms, for example "encrusting" sponges whose shapes follow those of the surfaces to which they attach. All freshwater and most shallow-water marine sponges have leuconid bodies. The networks of water passages in glass sponges are similar to the leuconid structure. In all three types of structure the cross-section area of the choanocyte-lined regions is much greater than that of the intake and outlet channels. This makes the flow slower near the choanocytes and thus makes it easier for them to trap food particles. For example in Leuconia, a small leuconoid sponge about 10 centimetres (3.9 in) tall and 1 centimetre (0.39 in) in diameter, water enters each of more than 80,000 intake canals at 6 cm per minute. However, because Leuconia has more than 2 million flagellated chambers whose combined diameter is much greater than that of the canals, water flow through chambers slows to 3.6 cm per hour, making it easy for choanocytes to capture food. All the water is expelled through a single osculum at about 8.5 cm per second, fast enough to carry waste products some distance away.
In zoology a skeleton is any fairly rigid structure of an animal, irrespective of whether it has joints and irrespective of whether it is biomineralized. The mesohyl functions as an endoskeleton in most sponges, and is the only skeleton in soft sponges that encrust hard surfaces such as rocks. More commonly the mesohyl is stiffened by mineral spicules, by spongin fibers or both. Spicules may be made of silica 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.
|Type of cells||Spicules||Spongin fibers||Massive exoskeleton||Body form|
|Calcarea||Single nucleus, single external membrane||Calcite
May be individual or large masses
Made of calcite if present.
|Asconoid, syconoid or leuconoid|
|Glass sponges||Mostly syncytia in all species||Silica
May be individual or fused
|Demosponges||Single nucleus, single external membrane||Silica||In many species||In some species.
Made of aragonite if present.
Although adult sponges are fundamentally sessile animals, some marine and freshwater species can move across the bottom at speeds of 1–4 millimetres (0.039–0.16 in) 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.
Sponges do not have distinct circulatory, respiratory, digestive, and excretory systems – instead the water flow system supports all these functions. They filter food particles out of the water flowing through them. Particles larger than 50 micrometers cannot enter the ostia and pinacocytes consume them by phagocytosis (engulfing and internal digestion). Particles from 0.5 to 50 micrometres (2.0×10−5 to 0.00197 in) are trapped in the ostia, which taper from the outer to inner ends. These particles are consumed by pinacocytes or by archaeocytes which partially extrude themselves through the walls of the ostia. Bacteria-sized particles, below 0.5 micrometers, pass through the ostia and are caught and consumed by choanocytes. Since the smallest particles are by far the most common, choanocytes typically capture 80% of a sponge's food supply. 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, and these tracks also move inert objects.
It used to be claimed that glass sponges could live on nutrients dissolved in sea water and were very averse to silt. 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.
Sponges' cells absorb oxygen by diffusion from the water flow system, into which carbon dioxide and other soluble waste products such as ammonia also diffuse. Archeocytes remove mineral particles that threaten to block the ostia, transport them through the mesohyl and generally dump them into the outgoing water current, although some species incorporate them into their skeletons.
A few species live in waters where the supply of food particles is very poor, prey on crustaceans and other small animals. Most belong to the family Cladorhizidae, but a few members of the Guitarridae and Esperiopsidae are also carnivores. In most cases little is known about how they actually capture prey, although some species are thought to use either sticky threads or hooked spicules. Most carnivorous sponges live in deep waters, up to 8,840 metres (5.49 mi), and the development of deep-ocean exploration techniques is expected to lead to the discovery of several more. However one species has been found in Mediterranean caves at depths of 17–23 metres (56–75 ft), alongside the more usual filter feeding sponges. The cave-dwelling predators capture crustaceans under 1 millimetre (0.039 in) long by entangling them with fine threads, digest them by enveloping them with further threads over the course of a few days, and then return to their normal shape; there is no evidence that they use venom.
Most known carnivorous sponges have completely lost the water flow system and choanocytes. However the genus Chondrocladia uses a highly modified water flow system to inflate balloon-like structures that are used for capturing prey.
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. In 2008 a University of Stuttgart team reported that spicules made of silica conduct light into the mesohyl, where the photosynthesizing endosymbionts live. Sponges that host photosynthesizing organisms are commonest in waters with relatively poor supplies of food particles, and often have leafy shapes that maximize the amount of sunlight they collect.
Sponges do not have the complex immune systems of most other animals. However they reject grafts from other species but accept them from other members of their own species. In a few marine species, gray cells play the leading role in rejection of foreign material. When invaded, they produce a chemical that stops movement of other cells in the affected area, thus preventing the intruder from using the sponge's internal transport systems. If the intrusion persists, the grey cells concentrate in the area and release toxins that kill all cells in the area. The "immune" system can stay in this activated state for up to three weeks.
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, and perhaps by predators. 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 though a fine cloth to regenerate. A sponge fragment can only regenerate if it contains both collencytes to produce mesohyl and archeocytes to produce all the other cell types. A very few species reproduce by budding.
Gemmules are "survival pods" which a few marine sponges and many freshwater species produce by the thousands when dying and which some, mainly freshwater species, regularly produce in autumn. Spongocytes make gemmules by wrapping shells of spongin, often reinforced with spicules, round clusters of archeocytes that are full of nutrients. Freshwater gemmules may also include phytosynthesizing symbionts. The gemmules then become dormant, and in this state can survive cold, drying out, lack of oxygen and extreme variations in salinity. Freshwater gemmules often do not revive until the temperature drops, stays cold for a few months and then reaches a near-"normal" level. When a gemmule germinates, the archeocytes round the outside of the cluster transform into pinacocytes, a membrane over a pore in the shell bursts, the cluster of cells slowly emerges, and most of the remaining archeocytes transform into other cell types needed to make a functioning sponge. Gemmules from the same species but different individuals can join forces to form one sponge. Some gemmules are retained within the parent sponge, and in spring it can be difficult to tell whether an old sponge has revived or been "recolonized" by its own gemmules.
Most sponges are hermaphrodites (function as both sexes simultaneously), although sponges have no gonads (reproductive organs). Sperm are produced by choanocytes or entire choanocyte chambers that sink into the mesohyl and form spermatic cysts while eggs are formed by transformation of archeocytes, or of choanocytes in some species. Each egg generally acquires a yolk by consuming "nurse cells". During spawning, sperm burst out of their cysts and are expelled via the osculum. If they contact another sponge of the same species, the water flow carries them to choanocytes that engulf them but, instead of digesting them, metamorphose to an ameboid form and carry the sperm through the mesohyl to eggs, which in most cases engulf the carrier and its cargo.
A few species release fertilized eggs into the water, but most retain the eggs until they hatch. There are four types of larvae, but all are balls of cells with an outer layer of cells whose flagellae 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.
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 0.2 millimetres (0.0079 in) per year and, if that rate is constant, specimens 1 metre (3.3 ft) 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.
Adult sponges lack neurons or any other kind of nervous tissue. However most species have the ability to perform movements that are co-ordinated all over their bodies, mainly contractions of the pinacocytes, squeezing the water channels and thus expelling excess sediment and other substances that may cause blockages. Some species can contract the osculum independently of the rest of the body. Sponges may also contract in order to reduce the area that is vulnerable to attack by predators. In cases where two sponges are fused, for example if there is a large but still unseparated bud, these contraction waves slowly become co-ordinated in both of the "Siamese twins". The co-ordinating mechanism is unknown, but may involve chemicals similar to neurotransmitters. 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. Myocytes are thought to be responsible for closing the osculum and for transmitting signals between different parts of the body.
Sponges contain genes very similar to those that contain the "recipe" for the post-synaptic density, an important signal-receiving structure in the neurons of all other animals. However in sponges these genes are only activated in "flask cells" that appear only in larvae and may provide some sensory capability while the larvae are swimming. This raises questions about whether flask cells represent the predecessors of true neurons or are evidence that sponges' ancestors had true neurons but lost them as they adapted to a sessile lifestyle.
Sponges are worldwide in their distribution, from the polar regions to the tropics. Most live in quiet, clear waters, because sediment stirred up by waves or currents would block their pores, making it difficult for them to feed and breathe. The greatest numbers of sponges are usually found on firm surfaces such as rocks, but some sponges can attach themselves to soft sediment by means of a root-like base.
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:
|Water type||Depth||Type of surface|
|Calcarea||Marine||less than 100 metres (330 ft)||Hard|
|Glass sponges||Marine||Deep||Soft or firm sediment|
|Demosponges||Marine, brackish; and about 150 freshwater species||Inter-tidal to abyssal; a carnivorous demosponge has been found at 8,840 metres (5.49 mi)||Any|
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 habits' resources are significant along Australia 's Great Barrier Reef but relatively minor in the Caribbean.
Many sponges shed spicules, forming a dense carpet several meters deep that keeps away echinoderms which would otherwise prey on the sponges. They also produce toxins that prevent other sessile organisms such as bryozoans or sea squirts from growing on or near them, making sponges very effective competitors for living space.
A few species, such as the Caribbean fire sponge Tedania ignis, cause a severe rash in humans who handle them. Turtles and some fish feed mainly on sponges. It is often said that sponges produce chemical defenses against such predators. However an experiment showed that there is no relationship between the toxicity of chemicals produced by sponges and how they taste to fish, which would diminish the usefulness of chemical defenses as deterrents. Predation by fish may even help to spread sponges by detaching fragments.
Sponge flies, also known as spongilla-flies (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 to pupate in.
The Caribbean chicken-liver sponge Chondrilla nucula secretes toxins that kill coral polyps, allowing the sponges to grow over the coral skeletons. Others, especially in the family Clionidae, use corrosive substances secreted by their archeocytes to tunnel into rocks, corals and the shells of dead molluscs. Sponges may remove up to 1 metre (3.3 ft) per year from reefs, creating visible notches just below low-tide level.
Caribbean sponges of the genus Aplysina suffer from Aplysina red band syndrome. This causes Aplysina to develop one or more rust-colored bands, sometimes with adjacent bands of necrotic tissue (dead). These lesions may completely encircle branches of the sponge. The disease appears to be contagious (spread by physical contact). The rust-colored bands are caused by a cyanobacterium, but it is unknown whether this organism actually causes the disease.
In addition to hosting photosynthesizing endosymbionts, sponges are noted for their wide range of collaborations with other organisms. The relatively large encrusting sponge Lissodendoryx colombiensis is most common on rocky surfaces, but has extended its range into seagrass meadows by letting itself be surrounded or overgrown by seagrass sponges, which are distasteful to the local starfish and therefore protect Lissodendoryx against them; in return the seagrass sponges get higher positions away from the sea-floor sediment.
Traces of the chemical 24-isopropylcholestane have been found in rocks formed . This is a stable derivative of 24-isopropylcholesterol, which is thought 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-isopropylcholesterol but that investigation of a wider range of choanoflagellates would be necessary in order to prove that the fossil 24-isopropylcholestane could only have been produced by demosponges.
Silica spicules like those of demosponges have been reported from Nevada 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. Fossils of glass sponges have been found from around in rocks in Australia, China and Mongolia. 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 . Freshwater sponges appear to be much younger, as the earliest known fossils date from the Mid-Eocene period about . Although about 90% of modern sponges are demosponges, fossilized remains of this type are less common than those of other types because their skeletons are composed of relatively soft spongin that does not fossilize well.
In the 1990s sponges were widely regarded as a monophyletic group, in other words all of them 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 ("true" animals, more complex than sponges) are more closely related to particular groups of sponges than to the rest of the sponges. 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. In 2007 one analysis based on comparisons of RNA and another based mainly on comparison of spicules concluded that demosponges and glass sponges are more closely related to each other than either is to calcareous sponges, which in turn are more closely related to Eumetazoa.
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 with those of Eumetazoa features that those 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 "type 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, in other words 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 most basal lineage of the 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. The results of such an analysis, published in 2009, suggest that a return to the previous view may be warranted. '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.
Archaeocyathids are very common fossils in rocks from the Early Cambrian about but are not found after the Late Cambrian. It has been suggested that they were produced by: sponges; cnidarians; algae; foraminiferans; a completely separate phylum of animals, Archaeocyatha; or even a completely separate kingdom of life, labelled Archaeata or Inferibionta. Since the 1990s archaeocyathids have been regarded as a distinctive group of sponges.
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.
For a long time sponges were assigned to a separate subkingdom, Parazoa ("beside the animals"), separate from the Eumetazoa which formed the rest of the kingdom Animalia. They are now classified as a phylum within Animalia, and divided into classes mainly according to the composition of their skeletons:
In the 1970s sponges with massive calcium carbonate skeletons were assigned to a separate class, Sclerospongiae, otherwise known as "coralline sponges". 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, of which: about 400 are glass sponges; about 500 are calcareous species; and the rest are demosponges. However some types of habitat, such as vertical rock and cave walls and galleries in rock and coral boulders, have been investigated very little, even in shallow seas.
A report in 1997 described use of sponges as a tool by bottlenose dolphins in Shark Bay. 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 behaviour, 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 behaviour to their daughters, and that all the sponge-users are closely related, suggesting that it is a fairly recent innovation.
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. Early Europeans used soft sponges for many purposes, including padding for helmets, portable drinking utensils and municipal water filters. Until the invention of synthetic sponges, they were used as cleaning tools, applicators for paints and ceramic glazes and discreet contraceptives. However by the mid-20th century, over-fishing brought both the animals and the industry close to extinction.
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.
Classes: †Archaeocyatha - Calcarea - Demospongiae - Hexactinellida - ?Sclerospongiae - Incertae sedis
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