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Starfish

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This article is about the animal. For the Spongebob character, see Patrick Star.
"Seastar" and "Sea Star" redirect here. For other uses, see SeaStar (disambiguation) and Starfish (disambiguation).
"Asteroidea" redirects here. For the Asteraceae subfamily, see Asteroideae.

Starfish
Temporal range: Ordovician–Recent
Fromia monilis
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Echinodermata
Subphylum: Asterozoa
Class: Asteroidea
Blainville, 1830
Child taxa and orders

† Calliasterellidae
† Trichasteropsida[2]

Starfish or sea stars are star-shaped echinoderms belonging to the class Asteroidea (/ˌæstəˈrɔɪdiə/). Common usage frequently finds these names being also applied to ophiuroids, which are correctly referred to as brittle stars or basket stars. Starfish are also known as asteroids due to being in the class Asteroidea. About 1,900 species of starfish live on the seabed in all the world's oceans, from warm, tropical zones to frigid, polar regions. They are found from the intertidal zone down to abyssal depths, at 6,000 m (20,000 ft) below the surface.

Starfish are marine invertebrates. They typically have a central disc and usually five arms, though some species have a larger number of arms. The aboral or upper surface may be smooth, granular or spiny, and is covered with overlapping plates. Many species are brightly coloured in various shades of red or orange, while others are blue, grey or brown. Starfish have tube feet operated by a hydraulic system and a mouth at the centre of the oral or lower surface. They are opportunistic feeders and are mostly predators on benthic invertebrates. Several species have specialized feeding behaviours including eversion of their stomachs and suspension feeding. They have complex life cycles and can reproduce both sexually and asexually. Most can regenerate damaged parts or lost arms and they can shed arms as a means of defense. The Asteroidea occupy several significant ecological roles. Starfish, such as the ochre sea star (Pisaster ochraceus) and the reef sea star (Stichaster australis), have become widely known as examples of the keystone species concept in ecology. The tropical crown-of-thorns starfish (Acanthaster planci) is a voracious predator of coral throughout the Indo-Pacific region, and the Northern Pacific seastar is on the list of the World's 100 Worst Invasive Alien Species.

The fossil record for starfish is ancient, dating back to the Ordovician around 450 million years ago, but it is rather sparse, as starfish tend to disintegrate after death. Only the ossicles and spines of the animal are likely to be preserved, making remains hard to locate. With their appealing symmetrical shape, starfish have played a part in literature, legend, design and popular culture. They are sometimes collected as curios, used in design or as logos, and in some cultures, despite possible toxicity, they are eaten.

Anatomy

Luidia maculata, a seven armed starfish

Most starfish have five arms that radiate from a central disc, but the number varies with the group. Some species have six or seven arms and others have 10–15 arms.[3] The Antarctic Labidiaster annulatus can have over fifty.[4]

Mapping the expression patterns of genes that express differently across the body axes suggests that one could think of the body of a starfish as a disembodied head walking about the sea floor on its lips. The known markers for trunk structures are expressed only in internal tissues rather than on the surface. Only the front part of the axis, which specifies head-related structures, is represented on the body surface.[5]

Body wall

Astropecten aranciacus ossicles
Pedicellariae and retracted papulae among the spines of Acanthaster planci
Pedicellaria and papulae of Asterias forbesi

The body wall consists of a thin cuticle, an epidermis consisting of a single layer of cells, a thick dermis formed of connective tissue and a thin coelomic myoepithelial layer, which provides the longitudinal and circular musculature. The dermis contains an endoskeleton of calcium carbonate components known as ossicles. These are honeycombed structures composed of calcite microcrystals arranged in a lattice.[6] They vary in form, with some bearing external granules, tubercles and spines, but most are tabular plates that fit neatly together in a tessellated manner and form the main covering of the aboral surface.[7] Some are specialised structures such as the madreporite (the entrance to the water vascular system), pedicellariae and paxillae.[6] Pedicellariae are compound ossicles with forceps-like jaws. They remove debris from the body surface and wave around on flexible stalks in response to physical or chemical stimuli while continually making biting movements. They often form clusters surrounding spines.[8][9] Paxillae are umbrella-like structures found on starfish that live buried in sediment. The edges of adjacent paxillae meet to form a false cuticle with a water cavity beneath in which the madreporite and delicate gill structures are protected. All the ossicles, including those projecting externally, are covered by the epidermal layer.[6]

Several groups of starfish, including Valvatida and Forcipulatida, possess pedicellariae.[8] In Forcipulatida, such as Asterias and Pisaster, they occur in pompom-like tufts at the base of each spine, whereas in the Goniasteridae, such as Hippasteria phrygiana, the pedicellariae are scattered over the body surface. Some are thought to assist in defence, while others aid in feeding or in the removal of organisms attempting to settle on the starfish's surface.[10] Some species like Labidiaster annulatus, Rathbunaster californicus and Novodinia antillensis use their large pedicellariae to capture small fish and crustaceans.[11]

There may also be papulae, thin-walled protrusions of the body cavity that reach through the body wall and extend into the surrounding water. These serve a respiratory function.[12] The structures are supported by collagen fibres set at right angles to each other and arranged in a three-dimensional web with the ossicles and papulae in the interstices. This arrangement enables both easy flexion of the arms by the starfish and the rapid onset of stiffness and rigidity required for actions performed under stress.[13]

Water vascular system

Arm tip with tube feet
Arm tip of Leptasterias polaris showing tube feet and eyespot

The water vascular system of the starfish is a hydraulic system made up of a network of fluid-filled canals and is concerned with locomotion, adhesion, food manipulation and gas exchange. Water enters the system through the madreporite, a porous, often conspicuous, sieve-like ossicle on the aboral surface. It is linked through a stone canal, often lined with calcareous material, to a ring canal around the mouth opening. A set of radial canals leads off this; one radial canal runs along the ambulacral groove in each arm. There are short lateral canals branching off alternately to either side of the radial canal, each ending in an ampulla. These bulb-shaped organs are joined to tube feet (podia) on the exterior of the animal by short linking canals that pass through ossicles in the ambulacral groove. There are usually two rows of tube feet but in some species, the lateral canals are alternately long and short and there appear to be four rows. The interior of the whole canal system is lined with cilia.[14]

When longitudinal muscles in the ampullae contract, valves in the lateral canals close and water is forced into the tube feet. These extend to contact the substrate. Although the tube feet resemble suction cups in appearance, the gripping action is a function of adhesive chemicals rather than suction.[15] Other chemicals and relaxation of the ampullae allow for release from the substrate. The tube feet latch on to surfaces and move in a wave, with one arm section attaching to the surface as another releases.[16][17] Some starfish turn up the tips of their arms while moving which gives maximum exposure of the sensory tube feet and the eyespot to external stimuli.[18]

Having descended from bilateral organisms, starfish may move in a bilateral fashion, particularly when hunting or in danger. When crawling, certain arms act as the leading arms, while others trail behind.[3][19][9] Most starfish cannot move quickly, a typical speed being that of the leather star (Dermasterias imbricata), which can manage just 15 cm (6 in) in a minute.[20] Some burrowing species from the genera Astropecten and Luidia have points rather than suckers on their long tube feet and are capable of much more rapid motion, "gliding" across the ocean floor. The sand star (Luidia foliolata) can travel at a speed of 2.8 m (9 ft 2 in) per minute.[21] When a starfish finds itself upside down, two adjacent arms are bent backwards to provide support, the opposite arm is used to stamp the ground while the two remaining arms are raised on either side; finally the stamping arm is released as the starfish turns itself over and recovers its normal stance.[19]

Apart from their function in locomotion, the tube feet act as accessory gills. The water vascular system serves to transport oxygen from, and carbon dioxide to, the tube feet and also nutrients from the gut to the muscles involved in locomotion. Fluid movement is bidirectional and initiated by cilia.[14] Gas exchange also takes place through other gills known as papulae, which are thin-walled bulges on the aboral surface of the disc and arms. Oxygen is transferred from these to the coelomic fluid, which acts as the transport medium for gasses. Oxygen dissolved in the water is distributed through the body mainly by the fluid in the main body cavity; the circulatory system may also play a minor role.[22]

Digestive system and excretion

Diagram of starfish anatomy
Aboral view of partially dissected starfish:
  1. Pyloric stomach
  2. Intestine and anus
  3. Rectal sac
  4. Stone canal
  5. Madreporite
  6. Pyloric caecum
  7. Digestive glands
  8. Cardiac stomach
  9. Gonad
  10. Radial canal
  11. Ambulacral ridge

The gut of a starfish occupies most of the disc and extends into the arms. The mouth is located in the centre of the oral surface, where it is surrounded by a tough peristomial membrane and closed with a sphincter. The mouth opens through a short oesophagus into a stomach divided by a constriction into a larger, eversible cardiac portion and a smaller pyloric portion. The cardiac stomach is glandular and pouched, and is supported by ligaments attached to ossicles in the arms so it can be pulled back into position after it has been everted. The pyloric stomach has two extensions into each arm: the pyloric caeca. These are elongated, branched hollow tubes that are lined by a series of glands, which secrete digestive enzymes and absorb nutrients from the food. A short intestine and rectum run from the pyloric stomach to open at a small anus at the apex of the aboral surface of the disc.[23]

Primitive starfish, such as Astropecten and Luidia, swallow their prey whole, and start to digest it in their cardiac stomachs. Shell valves and other inedible materials are ejected through their mouths. The semi-digested fluid is passed into their pyloric stomachs and caeca where digestion continues and absorption ensues.[23] In more advanced species of starfish, the cardiac stomach can be everted from the organism's body to engulf and digest food. When the prey is a clam or other bivalve, the starfish pulls with its tube feet to separate the two valves slightly, and inserts a small section of its stomach, which releases enzymes to digest the prey. The stomach and the partially digested prey are later retracted into the disc. Here the food is passed on to the pyloric stomach, which always remains inside the disc.[24] The retraction and contraction of the cardiac stomach is activated by a neuropeptide known as NGFFYamide.[25]

Because of this ability to digest food outside the body, starfish can hunt prey much larger than their mouths. Their diets include clams and oysters, arthropods, small fish and gastropod molluscs. Some starfish are not pure carnivores, supplementing their diets with algae or organic detritus. Some of these species are grazers, but others trap food particles from the water in sticky mucus strands that are swept towards the mouth along ciliated grooves.[23]

The main nitrogenous waste product is ammonia. Starfish have no distinct excretory organs; waste ammonia is removed by diffusion through the tube feet and papulae.[22] The body fluid contains phagocytic cells called coelomocytes, which are also found within the hemal and water vascular systems. These cells engulf waste material, and eventually migrate to the tips of the papulae, where a portion of body wall is nipped off and ejected into the surrounding water. Some waste may also be excreted by the pyloric glands and voided with the faeces.[22]

Starfish do not appear to have any mechanisms for osmoregulation, and keep their body fluids at the same salt concentration as the surrounding water. Although some species can tolerate relatively low salinity, the lack of an osmoregulation system probably explains why starfish are not found in fresh water or even in many estuarine environments.[22]

Sensory and nervous systems

Although starfish do not have many well-defined sense organs, they are sensitive to touch, light, temperature, orientation and the status of the water around them. The tube feet, spines and pedicellariae are sensitive to touch. The tube feet, especially those at the tips of the rays, are also sensitive to chemicals, enabling the starfish to detect odour sources such as food.[24] There are eyespots at the ends of the arms, each one made of 80–200 simple ocelli. These are composed of pigmented epithelial cells that respond to light and are covered by a thick, transparent cuticle that both protects the ocelli and acts to focus light. Many starfish also possess individual photoreceptor cells in other parts of their bodies and respond to light even when their eyespots are covered. Whether they advance or retreat depends on the species.[26]

While a starfish lacks a centralized brain, it has a complex nervous system with a nerve ring around the mouth and a radial nerve running along the ambulacral region of each arm parallel to the radial canal. The peripheral nerve system consists of two nerve nets: a sensory system in the epidermis and a motor system in the lining of the coelomic cavity. Neurons passing through the dermis connect the two.[26] The ring nerves and radial nerves have sensory and motor components and coordinate the starfish's balance and directional systems.[12] The sensory component receives input from the sensory organs while the motor nerves control the tube feet and musculature. The starfish does not have the capacity to plan its actions. If one arm detects an attractive odour, it becomes dominant and temporarily over-rides the other arms to initiate movement towards the prey. The mechanism for this is not fully understood.[26]

Circulatory system

The body cavity contains the circulatory or haemal system. The vessels form three rings: one around the mouth (the hyponeural haemal ring), another around the digestive system (the gastric ring) and the third near the aboral surface (the genital ring). The heart beats about six times a minute and is at the apex of a vertical channel (the axial vessel) that connects the three rings. At the base of each arm are paired gonads; a lateral vessel extends from the genital ring past the gonads to the tip of the arm. This vessel has a blind end and there is no continuous circulation of the fluid within it. This liquid does not contain a pigment and has little or no respiratory function but is probably used to transport nutrients around the body.[27]

Secondary metabolites

Starfish produce a large number of secondary metabolites in the form of lipids, including steroidal derivatives of cholesterol, and fatty acid amides of sphingosine. The steroids are mostly saponins, known as asterosaponins, and their sulphated derivatives. They vary between species and are typically formed from up to six sugar molecules (usually glucose and galactose) connected by up to three glycosidic chains. Long-chain fatty acid amides of sphingosine occur frequently and some of them have known pharmacological activity. Various ceramides are also known from starfish and a small number of alkaloids have also been identified. The functions of these chemicals in the starfish have not been fully investigated but most have roles in defence and communication. Some are feeding deterrents used by the starfish to discourage predation. Others are antifoulants and supplement the pedicellariae to prevent other organisms from settling on the starfish's aboral surface. Some are alarm pheromones and escape-eliciting chemicals, the release of which trigger responses in conspecific starfish but often produce escape responses in potential prey.[28] Research into the efficacy of these compounds for possible pharmacological or industrial use occurs worldwide.[29]

Life cycle

Sexual reproduction

Most species of starfish are gonochorous, there being separate male and female individuals. These are usually not distinguishable externally as the gonads cannot be seen, but their sex is apparent when they spawn.[30] Some species are simultaneous hermaphrodites, producing eggs and sperm at the same time, and in a few of these the same gonad, called an ovotestis, produces both eggs and sperm.[31] Other starfish are sequential hermaphrodites. Protandrous individuals of species like Asterina gibbosa start life as males before changing sex into females as they grow older. In some species such as Nepanthia belcheri, a large female can split in half and the resulting offspring are males. When these grow large enough they change back into females.[32]

Each starfish arm contains two gonads that release gametes through openings called gonoducts, located on the central disc between the arms. Fertilization is generally external but in a few species, internal fertilization takes place. In most species, the buoyant eggs and sperm are simply released into the water (free spawning) and the resulting embryos and larvae live as part of the plankton. In others, the eggs may be stuck to the undersides of rocks.[33] In certain species of starfish, the females brood their eggs – either by simply enveloping them[33] or by holding them in specialised structures. Brooding may be done in pockets on the starfish's aboral surface,[34][30] inside the pyloric stomach (Leptasterias tenera)[35] or even in the interior of the gonads themselves.[31] Those starfish that brood their eggs by "sitting" on them usually assume a humped posture with their discs raised off the substrate.[36] Pteraster militaris broods a few of its young and disperses the remaining eggs, that are too numerous to fit into its pouch.[34] In these brooding species, the eggs are relatively large, and supplied with yolk, and they generally develop directly into miniature starfish without an intervening larval stage.[31] The developing young are called lecithotrophic because they obtain their nutrition from the yolk as opposed to "planktotrophic" larvae that feed in the water column. In Parvulastra parvivipara, an intragonadal brooder, the young starfish obtain nutrients by eating other eggs and embryos in the brood pouch.[37] Brooding is especially common in polar and deep-sea species that live in environments unfavourable for larval development[30] and in smaller species that produce just a few eggs.[38][39]

In the tropics, a plentiful supply of phytoplankton is continuously available for starfish larvae to feed on. Spawning takes place at any time of year, each species having its own characteristic breeding season.[40] In temperate regions, the spring and summer brings an increase in food supplies. The first individual of a species to spawn may release a pheromone that serves to attract other starfish to aggregate and to release their gametes synchronously.[41] In other species, a male and female may come together and form a pair.[42][43] This behaviour is called pseudocopulation[44] and the male climbs on top, placing his arms between those of the female. When she releases eggs into the water, he is induced to spawn.[41] Starfish may use environmental signals to coordinate the time of spawning (day length to indicate the correct time of the year,[42] dawn or dusk to indicate the correct time of day), and chemical signals to indicate their readiness to breed. In some species, mature females produce chemicals to attract sperm in the sea water.[45]

Larval development

Starfish larvae
Three kinds of bilaterally symmetric starfish larvae (from left to right) scaphularia larva, bipinnaria larva, brachiolaria larva, all of Asterias sp. Painted by Ernst Haeckel

Most starfish embryos hatch at the blastula stage. The original ball of cells develops a lateral pouch, the archenteron. The entrance to this is known as the blastopore and it will later develop into the anus—together with chordates, echinoderms are deuterostomes, meaning the second (deutero) invagination becomes the mouth (stome); members of all other phyla are protostomes, and their first invagination becomes the mouth. Another invagination of the surface will fuse with the tip of the archenteron as the mouth while the interior section will become the gut. At the same time, a band of cilia develops on the exterior. This enlarges and extends around the surface and eventually onto two developing arm-like outgrowths. At this stage the larva is known as a bipinnaria. The cilia are used for locomotion and feeding, their rhythmic beat wafting phytoplankton towards the mouth.[8]

The next stage in development is a brachiolaria larva and involves the growth of three short, additional arms. These are at the anterior end, surround a sucker and have adhesive cells at their tips. Both bipinnaria and brachiolaria larvae are bilaterally symmetrical. When fully developed, the brachiolaria settles on the seabed and attaches itself with a short stalk formed from the ventral arms and sucker. Metamorphosis now takes place with a radical rearrangement of tissues. The left side of the larval body becomes the oral surface of the juvenile and the right side the aboral surface. Part of the gut is retained, but the mouth and anus move to new positions. Some of the body cavities degenerate but others become the water vascular system and the visceral coelom. The starfish is now pentaradially symmetrical. It casts off its stalk and becomes a free-living juvenile starfish about 1 mm (0.04 in) in diameter. Starfish of the order Paxillosida have no brachiolaria stage, with the bipinnaria larvae settling on the seabed and developing directly into juveniles.[8]

Asexual reproduction

Regeneration from an arm
"Comet" of Linckia guildingi, showing starfish body regrowing from a single arm
Main article: Asexual reproduction in starfish

Some species of starfish in the three families Asterinidae, Asteriidae and Solasteridae are able to reproduce asexually as adults either by fission of their central discs[46] or by autotomy of one or more of their arms.[47] Which of these processes occurs depends on the genus. Among starfish that are able to regenerate their whole body from a single arm, some can do so even from fragments just 1 cm (0.4 in) long.[48] Single arms that regenerate a whole individual are called comet forms. The division of the starfish, either across its disc or at the base of the arm, is usually accompanied by a weakness in the structure that provides a fracture zone.[49]

The larvae of several species of starfish can reproduce asexually before they reach maturity.[50] They do this by autotomising some parts of their bodies or by budding.[51] When such a larva senses that food is plentiful, it takes the path of asexual reproduction rather than normal development.[52] Though this costs it time and energy and delays maturity, it allows a single larva to give rise to multiple adults when the conditions are appropriate.[51]

Regeneration

Main article: Starfish regeneration
Arms being regenerated
Sunflower seastar regenerating missing arms

Some species of starfish have the ability to regenerate lost arms and can regrow an entire new limb given time.[48] A few can regrow a complete new disc from a single arm, while others need at least part of the central disc to be attached to the detached part.[22] Regrowth can take several months or years,[48] and starfish are vulnerable to infections during the early stages after the loss of an arm. A separated limb lives off stored nutrients until it regrows a disc and mouth and is able to feed again.[48] Other than fragmentation carried out for the purpose of reproduction, the division of the body may happen inadvertently due to part being detached by a predator, or part may be actively shed by the starfish in an escape response.[22] The loss of parts of the body is achieved by the rapid softening of a special type of connective tissue in response to nervous signals. This type of tissue is called catch connective tissue and is found in most echinoderms.[53] An autotomy-promoting factor has been identified which, when injected into another starfish, causes rapid shedding of arms.[54]

Lifespan

The lifespan of a starfish varies considerably between species, generally being longer in larger forms and in those with planktonic larvae. For example, Leptasterias hexactis broods a small number of large-yolked eggs. It has an adult weight of 20 g (0.7 oz), reaches sexual maturity in two years and lives for about ten years.[8] Pisaster ochraceus releases a large number of eggs into the sea each year and has an adult weight of up to 800 g (28 oz). It reaches maturity in five years and has a maximum recorded lifespan of 34 years.[8] The average lifespan of a starfish is 35 years, and larger starfish species typically live longer than their smaller counterparts.[55]

Ecology

Distribution and habitat

Echinoderms, including starfish, maintain a delicate internal electrolyte balance that is in equilibrium with sea water, making it impossible for them to live in a freshwater habitat.[16] Starfish species inhabit all of the world's oceans. Habitats range from tropical coral reefs, rocky shores, tidal pools, mud, and sand to kelp forests, seagrass meadows[56] and the deep-sea floor down to at least 6,000 m (20,000 ft).[57] The greatest diversity of species occurs in coastal areas.[56]

Diet

A starfish with its stomach turned outside its mouth to feed on coral
A Circeaster pullus starfish everting its stomach to feed on coral

Most species are generalist predators, eating microalgae, sponges, bivalves, snails and other small animals.[24][58] The crown-of-thorns starfish consumes coral polyps,[59] while other species are detritivores, feeding on decomposing organic material and faecal matter.[58][60] A few are suspension feeders, gathering in phytoplankton; Henricia and Echinaster often occur in association with sponges, benefiting from the water current they produce.[61] Various species have been shown to be able to absorb organic nutrients from the surrounding water, and this may form a significant portion of their diet.[61]

The processes of feeding and capture may be aided by special parts; Pisaster brevispinus, the short-spined pisaster from the West Coast of America, can use a set of specialized tube feet to dig itself deep into the soft substrate to extract prey (usually clams).[62] Grasping the shellfish, the starfish slowly pries open the prey's shell by wearing out its adductor muscle, and then inserts its everted stomach into the crack to digest the soft tissues. The gap between the valves need only be a fraction of a millimetre wide for the stomach to gain entry.[16] Cannibalism has been observed in juvenile sea stars as early as four days after metamorphosis.[63]

Ecological impact

Starfish on a wood pier
Starfish devouring mussel
Pisaster ochraceus consuming a mussel in central California

Starfish are keystone species in their respective marine communities. Their relatively large sizes, diverse diets and ability to adapt to different environments makes them ecologically important.[64] The term "keystone species" was in fact first used by Robert Paine in 1966 to describe a starfish, Pisaster ochraceus.[65] When studying the low intertidal coasts of Washington state, Paine found that predation by P. ochraceus was a major factor in the diversity of species. Experimental removals of this top predator from a stretch of shoreline resulted in lower species diversity and the eventual domination of Mytilus mussels, which were able to outcompete other organisms for space and resources.[66] Similar results were found in a 1971 study of Stichaster australis on the intertidal coast of the South Island of New Zealand. S. australis was found to have removed most of a batch of transplanted mussels within two or three months of their placement, while in an area from which S. australis had been removed, the mussels increased in number dramatically, overwhelming the area and threatening biodiversity.[67]

The feeding activity of the omnivorous starfish Oreaster reticulatus on sandy and seagrass bottoms in the Virgin Islands appears to regulate the diversity, distribution and abundance of microorganisms. These starfish engulf piles of sediment removing the surface films and algae adhering to the particles.[68] Organisms that dislike this disturbance are replaced by others better able to rapidly recolonise "clean" sediment. In addition, foraging by these migratory starfish creates diverse patches of organic matter, which may play a role in the distribution and abundance of organisms such as fish, crabs and sea urchins that feed on the sediment.[69]

Starfish sometimes have negative effects on ecosystems. Outbreaks of crown-of-thorns starfish have caused damage to coral reefs in Northeast Australia and French Polynesia.[59][70] A study in Polynesia found that coral cover declined drastically with the arrival of migratory starfish in 2006, dropping from 50% to under 5% in three years. This had a cascading effect on the whole benthic community and reef-feeding fish.[59] Asterias amurensis is one of a few echinoderm invasive species. Its larvae likely arrived in Tasmania from central Japan via water discharged from ships in the 1980s. The species has since grown in numbers to the point where they threaten commercially important bivalve populations. As such, they are considered pests,[71] and are on the Invasive Species Specialist Group's list of the world's 100 worst invasive species.[72]

Sea Stars (starfish) are the main predators of kelp-eating sea urchins. Satellite imagery shows that sea urchin populations have exploded due to starfish mass deaths, and that by 2021, sea urchins have destroyed 95% of California's kelp forests.[73]

Threats

Gull feeding on starfish
American herring gull feeding on a starfish

Starfish may be preyed on by conspecifics, sea anemones,[74] other starfish species, tritons, crabs, fish, gulls and sea otters.[38][71][75][76] Their first lines of defence are the saponins present in their body walls, which have unpleasant flavours.[77] Some starfish such as Astropecten polyacanthus also include powerful toxins such as tetrodotoxin among their chemical armoury, and the slime star can ooze out large quantities of repellent mucus. They also have body armour in the form of hard plates and spines.[78] The crown-of-thorns starfish is particularly unattractive to potential predators, being heavily defended by sharp spines, laced with toxins and sometimes with bright warning colours.[79] Other species protect their vulnerable tube feet and arm tips by lining their ambulacral grooves with spines and heavily plating their extremities.[78]

Warning coloration in the crown-of-thorns starfish

Several species sometimes suffer from a wasting condition caused by bacteria in the genus Vibrio;[75] however, a more widespread wasting disease, causing mass mortalities among starfish, appears sporadically. A paper published in November 2014 revealed the most likely cause of this disease to be a densovirus the authors named sea star-associated densovirus (SSaDV).[80] The protozoan Orchitophrya stellarum is known to infect the gonads of starfish and damage tissue.[75] Starfish are vulnerable to high temperatures. Experiments have shown that the feeding and growth rates of P. ochraceus reduce greatly when their body temperatures rise above 23 °C (73 °F) and that they die when their temperature rises to 30 °C (86 °F).[81][82] This species has a unique ability to absorb seawater to keep itself cool when it is exposed to sunlight by a receding tide.[83] It also appears to rely on its arms to absorb heat, so as to protect the central disc and vital organs like the stomach.[84]

Starfish and other echinoderms are sensitive to marine pollution.[85] The common starfish is considered to be a bioindicator for marine ecosystems.[86] A 2009 study found that P. ochraceus is unlikely to be affected by ocean acidification as severely as other marine animals with calcareous skeletons. In other groups, structures made of calcium carbonate are vulnerable to dissolution when the pH is lowered. Researchers found that when P. ochraceus were exposed to 21 °C (70 °F) and 770 ppm carbon dioxide (beyond rises expected in the next century), they were relatively unaffected. Their survival is likely due to the nodular nature of their skeletons, which are able to compensate for a shortage of carbonate by growing more fleshy tissue.[87]

Evolution

Fossil record

Starfish fossil
Starfish fossil, Riedaster reicheli, from the Plattenkalk Upper Jurassic limestone, Solnhofen
Ray fragment (oral surface; ambulacrum) of goniasterid asteroid; Zichor Formation (Coniacian, Upper Cretaceous), southern Israel.

Echinoderms first appeared in the fossil record in the Cambrian. The first known asterozoans were the Somasteroidea, which exhibit characteristics of both groups.[88] Starfish are infrequently found as fossils, possibly because their hard skeletal components separate as the animal decays. Despite this, there are a few places where accumulations of complete skeletal structures occur, fossilized in place in Lagerstätten – so-called "starfish beds".[89]

By the late Paleozoic, the crinoids and blastoids were the predominant echinoderms, and some limestones from this period are made almost entirely from fragments from these groups. In the two major extinction events that occurred during the late Devonian and late Permian, the blastoids were wiped out and only a few species of crinoids survived.[88] Many starfish species also became extinct in these events, but afterwards the surviving few species diversified rapidly within about sixty million years during the Early Jurassic and the beginning of the Middle Jurassic.[90][91] A 2012 study found that speciation in starfish can occur rapidly. During the last 6,000 years, divergence in the larval development of Cryptasterina hystera and Cryptasterina pentagona has taken place, the former adopting internal fertilization and brooding and the latter remaining a broadcast spawner.[92]

Diversity

See also: List of echinodermata orders
Video showing the tube feet movement of a starfish
Close up starfish at Wakatobi National Park, 2018

The scientific name Asteroidea was given to starfish by the French zoologist de Blainville in 1830.[93] It is derived from the Greek aster, ἀστήρ (a star) and the Greek eidos, εἶδος (form, likeness, appearance).[94] The class Asteroidea belongs to the phylum Echinodermata. As well as the starfish, the echinoderms include sea urchins, sand dollars, brittle and basket stars, sea cucumbers and crinoids. The larvae of echinoderms have bilateral symmetry, but during metamorphosis this is replaced with radial symmetry, typically pentameric.[12] Adult echinoderms are characterized by having a water vascular system with external tube feet and a calcareous endoskeleton consisting of ossicles connected by a mesh of collagen fibres.[95] Starfish are included in the subphylum Asterozoa, the characteristics of which include a flattened, star-shaped body as adults consisting of a central disc and multiple radiating arms. The subphylum includes the two classes of Asteroidea, the starfish, and Ophiuroidea, the brittle stars and basket stars. Asteroids have broad-based arms with skeletal support provided by calcareous plates in the body wall[90] while ophiuroids have clearly demarcated slender arms strengthened by paired fused ossicles forming jointed "vertebrae".[96]

The starfish are a large and diverse class with over 1,900 living species. There are seven extant orders, Brisingida, Forcipulatida, Notomyotida, Paxillosida, Spinulosida, Valvatida and Velatida[1] and two extinct ones, Calliasterellidae and Trichasteropsida.[2] Living asteroids, the Neoasteroidea, are morphologically distinct from their forerunners in the Paleozoic. The taxonomy of the group is relatively stable but there is ongoing debate about the status of the Paxillosida, and the deep-water sea daisies, though clearly Asteroidea and currently included in Velatida, do not fit easily in any accepted lineage. Phylogenetic data suggests that they may be a sister group, the Concentricycloidea, to the Neoasteroidea, or that the Velatida themselves may be a sister group.[91]

18-arm starfish
A large 18-armed member of Brisingida

Living groups

Brisingida (2 families, 17 genera, 111 species)[97]
Species in this order have a small, inflexible disc and 6–20 long, thin arms, which they use for suspension feeding. They have a single series of marginal plates, a fused ring of disc plates, a reduced number of aboral plates, crossed pedicellariae, and several series of long spines on the arms. They live almost exclusively in deep-sea habitats, although a few live in shallow waters in the Antarctic.[98][99] In some species, the tube feet have rounded tips and lack suckers.[100]
Common starfish
Common starfish, a member of Forcipulatida
Forcipulatida (6 families, 63 genera, 269 species)[101]
Species in this order have distinctive pedicellariae, consisting of a short stalk with three skeletal ossicles. They tend to have robust bodies[102] and have tube feet with flat-tipped suckers usually arranged in four rows.[100] The order includes well-known species from temperate regions, including the common starfish of North Atlantic coasts and rock pools, as well as cold-water and abyssal species.[103]
Notomyotida (1 family, 8 genera, 75 species)[104]
These starfish are deep-sea dwelling and have particularly flexible arms. The inner dorso-lateral surfaces of the arms contain characteristic longitudinal muscle bands.[1] In some species, the tube feet lack suckers.[100]
Magnificent star
Magnificent star, a member of Paxillosida
Paxillosida (7 families, 48 genera, 372 species)[105]
This is a primitive order and members do not extrude their stomach when feeding, lack an anus and have no suckers on their tube feet. Papulae are plentiful on their aboral surface and they possess marginal plates and paxillae. They mostly inhabit soft-bottomed areas of sand or mud.[8] There is no brachiolaria stage in their larval development.[106] The comb starfish (Astropecten polyacanthus) is a member of this order.[107]
Red-knobbed starfish
Red-knobbed starfish, a member of Valvatida
Spinulosida (1 family, 8 genera, 121 species)[108]
Most species in this order lack pedicellariae and all have a delicate skeletal arrangement with small or no marginal plates on the disc and arms. They have numerous groups of short spines on the aboral surface.[109][110] This group includes the red starfish Echinaster sepositus.[111]
Valvatida (16 families, 172 genera, 695 species)[112]
Most species in this order have five arms and two rows of tube feet with suckers. There are conspicuous marginal plates on the arms and disc. Some species have paxillae and in some, the main pedicellariae are clamp-like and recessed into the skeletal plates.[110] This group includes the cushion stars,[113] the leather star[114] and the sea daisies.[115]
Velatida (4 families, 16 genera, 138 species)[116]
This order of starfish consists mostly of deep-sea and other cold-water starfish often with a global distribution. The shape is pentagonal or star-shaped with five to fifteen arms. They mostly have poorly developed skeletons with papulae widely distributed on the aboral surface and often spiny pedicellariae.[117] This group includes the slime star.[118]

Extinct groups

Extinct groups within the Asteroidea include:[2]

Phylogeny

External

Starfish are deuterostome animals, like the chordates. A 2014 analysis of 219 genes from all classes of echinoderms gives the following phylogenetic tree.[121] The times at which the clades diverged are shown under the labels in millions of years ago (mya).

Bilateria

Internal

The phylogeny of the Asteroidea has been difficult to resolve, with visible (morphological) features proving inadequate, and the question of whether traditional taxa are clades in doubt.[2] The phylogeny proposed by Gale in 1987 is:[2][122]

† Palaeozoic Asteroids

Paxillosida

Valvatida, including Velatida, Spinulosida (not a clade)[2]

Forcipulatida, including Brisingida

The phylogeny proposed by Blake in 1987 is:[2][123]

† Palaeozoic Asteroids

† Calliasterellidae

† Compasteridae

† Trichasteropsida

Brisingida

Forcipulatida

Spinulosida

Velatida

Notomyotida

Valvatida

Paxillosida

Later work making use of molecular evidence, with or without the use of morphological evidence, had by 2000 failed to resolve the argument.[2] In 2011, on further molecular evidence, Janies and colleagues noted that the phylogeny of the echinoderms "has proven difficult", and that "the overall phylogeny of extant echinoderms remains sensitive to the choice of analytical methods". They presented a phylogenetic tree for the living Asteroidea only; using the traditional names of starfish orders where possible, and indicating "part of" otherwise, the phylogeny is shown below. The Solasteridae are split from the Velatida, and the old Spinulosida is broken up.[124]

Solasteridae and part of Spinulosida, e.g. Stegnaster and part of Valvatida, e.g. Asterina

Odontasteridae, which was a part of Valvatida

Paxillosida

part of Spinulosida, e.g. Echinaster, part of Valvatida, e.g. Archaster

Forcipulatida

Brisingida with part of Velatida, e.g. Caymanostella and part of Forcipulatida, e.g. Stichaster

Velatida except for Solasteridae

Notomyotida (not analysed)

Human relations

In research

A calcified starfish from Los Roques Archipelago

Starfish are deuterostomes, closely related, together with all other echinoderms, to chordates, and are used in reproductive and developmental studies. Female starfish produce large numbers of oocytes that are easily isolated; these can be stored in a pre-meiosis phase and stimulated to complete division by the use of 1-methyladenine.[125] Starfish oocytes are well suited for this research as they are large and easy to handle, transparent, simple to maintain in sea water at room temperature, and they develop rapidly.[126] Asterina pectinifera, used as a model organism for this purpose, is resilient and easy to breed and maintain in the laboratory.[127]

Another area of research is the ability of starfish to regenerate lost body parts. The stem cells of adult humans are incapable of much differentiation and understanding the regrowth, repair and cloning processes in starfish may have implications for human medicine.[128]

Starfish also have an unusual ability to expel foreign objects from their bodies, which makes them difficult to tag for research tracking purposes.[129]

In legend and culture

A starfish with five legs. Used as an illustration of "Hope in God", a poem by Lydia Sigourney which appeared in Poems for the Sea, 1850

An aboriginal Australian fable retold by the Welsh school headmaster William Jenkyn Thomas (1870–1959)[130] tells how some animals needed a canoe to cross the ocean. Whale had one but refused to lend it, so Starfish kept him busy, telling him stories and grooming him to remove parasites, while the others stole the canoe. When Whale realized the trick he beat Starfish ragged, which is how Starfish still is today.[131]

In 1900, the scholar Edward Tregear documented The Creation Song, which he describes as "an ancient prayer for the dedication of a high chief" of Hawaii. Among the "uncreated gods" described early in the song are the male Kumulipo ("Creation") and the female Poele, both born in the night, a coral insect, the earthworm, and the starfish.[132]

red watercolor painting of a starfish
1860 watercolor painting of a starfish by Jacques Burkhardt

Georg Eberhard Rumpf's 1705 The Ambonese Curiosity Cabinet describes the tropical varieties of Stella Marina or Bintang Laut, "Sea Star", in Latin and Malay respectively, known in the waters around Ambon. He writes that the Histoire des Antilles reports that when the sea stars "see thunder storms approaching, [they] grab hold of many small stones with their little legs, looking to ... hold themselves down as if with anchors".[133]

Starfish is the title of novels by Peter Watts[134] and Jennie Orbell,[135] and in 2012, Alice Addison wrote a non-fiction book titled Starfish: A Year in the Life of Bereavement and Depression.[136] The Starfish and the Spider is a 2006 business management book by Ori Brafman and Rod Beckstrom; its title alludes to the ability of the starfish to regenerate itself because of its decentralized nervous system, and the book suggests ways that a decentralized organisation may flourish.[137]

In the Nickelodeon animated television series SpongeBob SquarePants, the eponymous character's best friend is a dim-witted starfish, Patrick Star.[138]

As food

Fried starfish skewers in China

Starfish are widespread in the oceans, but are only occasionally used as food. There may be good reason for this: the bodies of numerous species are dominated by bony ossicles, and the body wall of many species contains saponins, which have an unpleasant taste,[77] and others contain tetrodotoxins which are poisonous.[139] Some species that prey on bivalve molluscs can transmit paralytic shellfish poisoning.[140] Georg Eberhard Rumpf found few starfish being used for food in the Indonesian archipelago, other than as bait in fish traps, but on the island of "Huamobel" [sic] the people cut them up, squeeze out the "black blood" and cook them with sour tamarind leaves; after resting the pieces for a day or two, they remove the outer skin and cook them in coconut milk.[133] Starfish are sometimes eaten in China,[141] Japan[142][143] and in Micronesia.[144]

As collectables

Starfish are in some cases taken from their habitat and sold to tourists as souvenirs, ornaments, curios or for display in aquariums. In particular, Oreaster reticulatus, with its easily accessed habitat and conspicuous coloration, is widely collected in the Caribbean. In the early to mid 20th century, this species was common along the coasts of the West Indies, but collection and trade have severely reduced its numbers. In the State of Florida, O. reticulatus is listed as endangered and its collection is illegal. Nevertheless, it is still sold throughout its range and beyond.[76] A similar phenomenon exists in the Indo-Pacific for species such as Protoreaster nodosus.[145]

Starfish on sale as souvenirs in Cyprus

In industry and military history

With its multiple arms, the starfish provides a popular metaphor for computer networks,[146] companies[147][148] and software tools.[149] It is also the name of a seabed imaging system and company.[150]

Starfish has repeatedly been chosen as a name in military history. Three ships of the Royal Navy have borne the name HMS Starfish: an A-class destroyer launched in 1894;[151] an R-class destroyer launched in 1916;[152] and an S-class submarine launched in 1933 and lost in 1940.[153] In World War II, Starfish sites were large-scale night-time decoys created during The Blitz to simulate burning British cities.[154] Starfish Prime was a high-altitude nuclear test conducted by the United States on 9 July 1962.[155]

References

  1. ^ a b c Sweet, Elizabeth (22 November 2005). "Fossil Groups: Modern forms: Asteroids: Extant Orders of the Asteroidea". University of Bristol. Archived from the original on 14 July 2007. Retrieved 31 May 2016.
  2. ^ a b c d e f g h i Knott, Emily (7 October 2004). "Asteroidea. Sea stars and starfishes". Tree of Life web project. Retrieved 10 May 2013.
  3. ^ a b Wu, Liang; Ji, Chengcheng; Wang, Sishuo; Lv, Jianhao (2012). "The advantages of the pentameral symmetry of the starfish". arXiv:1202.2219 [q-bio.PE].
  4. ^ Prager, Ellen (2011). Sex, Drugs, and Sea Slime: The Oceans' Oddest Creatures and Why They Matter. University of Chicago Press. p. 74. ISBN 978-0-2266-7872-6.
  5. ^ Lacalli, T. (2023). A radical evolutionary makeover gave echinoderms their unusual body plan. Nature. https://doi.org/10.1038/d41586-023-03123-1
  6. ^ a b c Ruppert et al., 2004. p. 877
  7. ^ Sweat, L. H. (31 October 2012). "Glossary of terms: Phylum Echinodermata". Smithsonian Institution. Retrieved 12 May 2013.
  8. ^ a b c d e f g Ruppert et al, 2004. pp. 887–889
  9. ^ a b Carefoot, Tom. "Pedicellariae". Sea Stars: Predators & Defenses. A Snail's Odyssey. Archived from the original on 16 March 2013. Retrieved 11 May 2013.
  10. ^ Barnes, R. S. K.; Callow, P.; Olive, P. J. W. (1988). The Invertebrates: a new synthesis. Oxford: Blackwell Scientific Publications. pp. 158–160. ISBN 978-0-632-03125-2.
  11. ^ Lawrence, J. M. (24 January 2013). "The Asteroid Arm". Starfish: Biology and Ecology of the Asteroidea. JHU Press. pp. 15–23. ISBN 9781421407876. in Lawrence (2013)
  12. ^ a b c Fox, Richard (25 May 2007). "Asterias forbesi". Invertebrate Anatomy OnLine. Lander University. Retrieved 19 May 2012.
  13. ^ O'Neill, P. (1989). "Structure and mechanics of starfish body wall". Journal of Experimental Biology. 147: 53–89. doi:10.1242/jeb.147.1.53. PMID 2614339.
  14. ^ a b Ruppert et al., 2004. pp. 879–883
  15. ^ Hennebert, E.; Santos, R.; Flammang, P. (2012). "Echinoderms don't suck: evidence against the involvement of suction in tube foot attachment" (PDF). Zoosymposia. 1: 25–32. doi:10.11646/zoosymposia.7.1.3.
  16. ^ a b c Dorit, R. L.; Walker, W. F.; Barnes, R. D. (1991). Zoology. Saunders College Publishing. p. 782. ISBN 978-0-03-030504-7.
  17. ^ Cavey, Michael J.; Wood, Richard L. (1981). "Specializations for excitation-contraction coupling in the podial retractor cells of the starfish Stylasterias forreri". Cell and Tissue Research. 218 (3): 475–485. doi:10.1007/BF00210108. PMID 7196288. S2CID 21844282.
  18. ^ Carefoot, Tom. "Tube feet". Sea Stars: Locomotion. A Snail's Odyssey. Archived from the original on 21 October 2013. Retrieved 11 May 2013.
  19. ^ a b Chengcheng, J.; Wu, L.; Zhoa, W.; Wang, S.; Lv, J. (2012). "Echinoderms have bilateral tendencies". PLOS ONE. 7 (1): e28978. arXiv:1202.4214. Bibcode:2012PLoSO...728978J. doi:10.1371/journal.pone.0028978. PMC 3256158. PMID 22247765.
  20. ^ "Leather star - Dermasterias imbricata". Sea Stars of the Pacific Northwest. Archived from the original on 9 September 2012. Retrieved 27 September 2012.
  21. ^ McDaniel, Daniel. "Sand star - Luidia foliolata". Sea Stars of the Pacific Northwest. Archived from the original on 9 September 2012. Retrieved 26 September 2012.
  22. ^ a b c d e f Ruppert et al., 2004. pp. 886–887
  23. ^ a b c Ruppert et al., 2004. p. 885
  24. ^ a b c Carefoot, Tom. "Adult feeding". Sea Stars: Feeding, growth, & regeneration. A Snail's Odyssey. Archived from the original on 12 May 2013. Retrieved 13 July 2013.
  25. ^ Semmens, Dean C.; Dane, Robyn E.; Pancholi, Mahesh R.; Slade, Susan E.; Scrivens, James H.; Elphick, Maurice R. (2013). "Discovery of a novel neurophysin-associated neuropeptide that triggers cardiac stomach contraction and retraction in starfish". Journal of Experimental Biology. 216 (21): 4047–4053. doi:10.1242/jeb.092171. PMID 23913946. S2CID 19175526.
  26. ^ a b c Ruppert et al., 2004. pp. 883–884
  27. ^ Ruppert et al., 2004. p. 886
  28. ^ McClintock, James B.; Amsler, Charles D.; Baker, Bill J. (2013). "8: Chemistry and Ecological Role of Starfish Secondary Metabolites". In Lawrence, John M. (ed.). Starfish: Biology and Ecology of the Asteroidea. JHU Press. ISBN 978-1-4214-1045-6.
  29. ^ Zhang, Wen; Guo, Yue-Wei; Gu, Yucheng (2006). "Secondary metabolites from the South China Sea invertebrates: chemistry and biological activity". Current Medicinal Chemistry. 13 (17): 2041–2090. doi:10.2174/092986706777584960. PMID 16842196.
  30. ^ a b c Ruppert et al., 2004. pp. 887–888
  31. ^ a b c Byrne, Maria (2005). "Viviparity in the sea star Cryptasterina hystera (Asterinidae): conserved and modified features in reproduction and development". Biological Bulletin. 208 (2): 81–91. CiteSeerX 10.1.1.334.314. doi:10.2307/3593116. JSTOR 3593116. PMID 15837957. S2CID 16302535.
  32. ^ Ottesen, P. O.; Lucas, J. S. (1982). "Divide or broadcast: interrelation of asexual and sexual reproduction in a population of the fissiparous hermaphroditic seastar Nepanthia belcheri (Asteroidea: Asterinidae)". Marine Biology. 69 (3): 223–233. Bibcode:1982MarBi..69..223O. doi:10.1007/BF00397488. S2CID 84885523.
  33. ^ a b Crump, R. G.; Emson, R. H. (1983). "The natural history, life history and ecology of the two British species of Asterina" (PDF). Field Studies. 5 (5): 867–882. Retrieved 27 July 2011.
  34. ^ a b McClary, D. J.; Mladenov, P. V. (1989). "Reproductive pattern in the brooding and broadcasting sea star Pteraster militaris". Marine Biology. 103 (4): 531–540. Bibcode:1989MarBi.103..531M. doi:10.1007/BF00399585. S2CID 84867808.
  35. ^ Hendler, Gordon; Franz, David R. (1982). "The biology of a brooding seastar, Leptasterias tenera, in Block Island". Biological Bulletin. 162 (3): 273–289. doi:10.2307/1540983. JSTOR 1540983.
  36. ^ Chia, Fu-Shiang (1966). "Brooding behavior of a six-rayed starfish, Leptasterias hexactis". Biological Bulletin. 130 (3): 304–315. doi:10.2307/1539738. JSTOR 1539738.
  37. ^ Byrne, M. (1996). "Viviparity and intragonadal cannibalism in the diminutive sea stars Patiriella vivipara and P. parvivipara (family Asterinidae)". Marine Biology. 125 (3): 551–567. Bibcode:1996MarBi.125..551B. doi:10.1007/BF00353268. S2CID 83110156.
  38. ^ a b Gaymer, C. F.; Himmelman, J. H. (2014). "Leptasterias polaris". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. pp. 182–84. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  39. ^ Mercier, A.; Hamel J-F. (2014). "Reproduction in Asteroidea". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. p. 37. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  40. ^ Thorson, Gunnar (1950). "Reproductive and larval ecology of marine bottom invertebrates". Biological Reviews. 25 (1): 1–45. doi:10.1111/j.1469-185X.1950.tb00585.x. PMID 24537188. S2CID 43678161.
  41. ^ a b Beach, D. H.; Hanscomb, N. J.; Ormond, R. F. G. (1975). "Spawning pheromone in crown-of-thorns starfish". Nature. 254 (5496): 135–136. Bibcode:1975Natur.254..135B. doi:10.1038/254135a0. PMID 1117997. S2CID 4278163.
  42. ^ a b Bos A.R.; G.S. Gumanao; B. Mueller; M.M. Saceda (2013). "Size at maturation, sex differences, and pair density during the mating season of the Indo-Pacific beach star Archaster typicus (Echinodermata: Asteroidea) in the Philippines". Invertebrate Reproduction and Development. 57 (2): 113–119. Bibcode:2013InvRD..57..113B. doi:10.1080/07924259.2012.689264. S2CID 84274160.
  43. ^ Run, J. -Q.; Chen, C. -P.; Chang, K. -H.; Chia, F. -S. (1988). "Mating behaviour and reproductive cycle of Archaster typicus (Echinodermata: Asteroidea)". Marine Biology. 99 (2): 247–253. Bibcode:1988MarBi..99..247R. doi:10.1007/BF00391987. ISSN 0025-3162. S2CID 84566087.
  44. ^ Keesing, John K.; Graham, Fiona; Irvine, Tennille R.; Crossing, Ryan (2011). "Synchronous aggregated pseudo-copulation of the sea star Archaster angulatus Müller & Troschel, 1842 (Echinodermata: Asteroidea) and its reproductive cycle in south-western Australia". Marine Biology. 158 (5): 1163–1173. Bibcode:2011MarBi.158.1163K. doi:10.1007/s00227-011-1638-2. S2CID 84926100.
  45. ^ Miller, Richard L. (12 October 1989). "Evidence for the presence of sexual pheromones in free-spawning starfish". Journal of Experimental Marine Biology and Ecology. 130 (3): 205–221. Bibcode:1989JEMBE.130..205M. doi:10.1016/0022-0981(89)90164-0.
  46. ^ Achituv, Y.; Sher, E. (1991). "Sexual reproduction and fission in the sea star Asterina burtoni from the Mediterranean coast of Israel". Bulletin of Marine Science. 48 (3): 670–679.
  47. ^ Rubilar, Tamara; Pastor, Catalina; Diaz de Vivar, Enriqueta (30 January 2006). "Timing of fission in the starfish Allostichaster capensis (Echinodermata:Asteroidea) in laboratory" (PDF). Revista de Biología Tropical (53 (Supplement 3)): 299–303.
  48. ^ a b c d Edmondson, C. H. (1935). "Autotomy and regeneration of Hawaiian starfishes" (PDF). Bishop Museum Occasional Papers. 11 (8): 3–20.
  49. ^ Carnevali, Candia; Bonasoro F. (2001). "Introduction to the biology of regeneration in echinoderms". Microscopy Research and Technique. 55 (6): 365–368. doi:10.1002/jemt.1184. PMID 11782068. S2CID 31052874.
  50. ^ Eaves, Alexandra A.; Palmer, A. Richard (2003). "Reproduction: widespread cloning in echinoderm larvae". Nature. 425 (6954): 146. Bibcode:2003Natur.425..146E. doi:10.1038/425146a. ISSN 0028-0836. PMID 12968170. S2CID 4430104.
  51. ^ a b Jaeckle, William B. (1994). "Multiple modes of asexual reproduction by tropical and subtropical sea star larvae: an unusual adaptation for genet dispersal and survival". Biological Bulletin. 186 (1): 62–71. doi:10.2307/1542036. JSTOR 1542036. PMID 29283296.
  52. ^ Vickery, M. S.; McClintock, J. B. (1 December 2000). "Effects of food concentration and availability on the incidence of cloning in planktotrophic larvae of the sea star Pisaster ochraceus". The Biological Bulletin. 199 (3): 298–304. doi:10.2307/1543186. JSTOR 1543186. PMID 11147710.
  53. ^ Hayashi, Yutaka; Motokawa, Tatsuo (1986). "Effects of ionic environment on viscosity of catch connective tissue in holothurian body wall". Journal of Experimental Biology. 125 (1): 71–84. doi:10.1242/jeb.125.1.71. ISSN 0022-0949.
  54. ^ Mladenov, Philip V.; Igdoura, Suleiman; Asotra, Satish; Burke, Robert D. (1989). "Purification and partial characterization of an autotomy-promoting factor from the sea star Pycnopodia helianthoides". Biological Bulletin. 176 (2): 169–175. doi:10.2307/1541585. ISSN 0006-3185. JSTOR 1541585. Archived from the original on 23 September 2015. Retrieved 12 July 2013.
  55. ^ template, barebone (4 September 2019). "Fun facts about Starfish". National Marine Aquarium. Retrieved 17 April 2024.
  56. ^ a b "Asteroidea (Sea Stars)". Encyclopedia.com. Grzimek's Animal Life Encyclopedia. 2004. Retrieved 14 July 2012.
  57. ^ Mah, Christopher; Nizinski, Martha; Lundsten, Lonny (2010). "Phylogenetic revision of the Hippasterinae (Goniasteridae; Asteroidea): systematics of deep sea corallivores, including one new genus and three new species". Zoological Journal of the Linnean Society. 160 (2): 266–301. doi:10.1111/j.1096-3642.2010.00638.x.
  58. ^ a b Pearse, J. S. (2014). "Odontaster validus". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. pp. 124–25. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  59. ^ a b c Kayal, Mohsen; Vercelloni, Julie; Lison de Loma, Thierry; Bosserelle, Pauline; Chancerelle, Yannick; Geoffroy, Sylvie; Stievenart, Céline; Michonneau, François; Penin, Lucie; Planes, Serge; Adjeroud, Mehdi (2012). Fulton, Christopher (ed.). "Predator crown-of-thorns starfish (Acanthaster planci) outbreak, mass mortality of corals, and cascading effects on reef fish and benthic communities". PLOS ONE. 7 (10): e47363. Bibcode:2012PLoSO...747363K. doi:10.1371/journal.pone.0047363. PMC 3466260. PMID 23056635.
  60. ^ Turner, R. L. (2014). "Echinaster". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. pp. 206–207. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2012)
  61. ^ a b Florkin, Marcel (2012). Chemical Zoology V3: Echinnodermata, Nematoda, and Acanthocephala. Elsevier. pp. 75–77. ISBN 978-0-323-14311-0.
  62. ^ Nybakken, James W.; Bertness, Mark D. (1997). Marine Biology: An Ecological Approach. Addison-Wesley Educational Publishers. p. 174. ISBN 978-0-8053-4582-7.
  63. ^ McClain, Joseph (5 April 2021). "Researcher reports cannibalistic echinoderm underwater dwellers". phys.org. Retrieved 6 April 2021.
  64. ^ Menage, B. A.; Sanford, E. (2014). "Ecological Role of Sea Stars from Populations to Meta-ecosystems". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. p. 67. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  65. ^ Wagner, S. C. (2012). "Keystone Species". Nature Education Knowledge. Retrieved 16 May 2013.
  66. ^ Paine, R. T. (1966). "Food web complexity and species diversity". American Naturalist. 100 (190): 65–75. doi:10.1086/282400. JSTOR 2459379. S2CID 85265656.
  67. ^ Paine, R. T. (1971). "A short-term experimental investigation of resource partitioning in a New Zealand rocky intertidal habitat". Ecology. 52 (6): 1096–1106. Bibcode:1971Ecol...52.1096P. doi:10.2307/1933819. JSTOR 1933819.
  68. ^ Wullf, L. (1995). "Sponge-feeding by the Caribbean starfish Oreaster reticulatus". Marine Biology. 123 (2): 313–325. Bibcode:1995MarBi.123..313W. doi:10.1007/BF00353623. S2CID 85726832.
  69. ^ Scheibling, R. E. (1980). "Dynamics and feeding activity of high-density aggregations of Oreaster reticulatus (Echinodermata: Asteroidea) in a sand patch habitat". Marine Ecology Progress Series. 2: 321–27. Bibcode:1980MEPS....2..321S. doi:10.3354/meps002321.
  70. ^ Brodie J, Fabricius K, De'ath G, Okaji K (2005). "Are increased nutrient inputs responsible for more outbreaks of crown-of-thorns starfish? An appraisal of the evidence". Marine Pollution Bulletin. 51 (1–4): 266–78. Bibcode:2005MarPB..51..266B. doi:10.1016/j.marpolbul.2004.10.035. PMID 15757727.
  71. ^ a b Byrne, M.; O'Hara, T. D.; Lawrence, J. M. (2014). "Asterias amurensis". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. pp. 177–179. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  72. ^ "100 of the World's Worst Invasive Alien Species". Global Invasive Species Database. Archived from the original on 29 April 2015. Retrieved 16 July 2010.
  73. ^ Whang, Oliver (5 December 2022). "The Missing Mammal (the extinct: Steller's sea cow) That May Have Shaped California's Kelp Forests". The New York Times. Retrieved 5 December 2022.
  74. ^ "Fact Sheet: Sea Anemones". Marine Biological Association. 21 February 2017. Archived from the original on 24 December 2019. Retrieved 10 June 2019.
  75. ^ a b c Robles, C. (2014). "Pisaster ochraceus". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. pp. 166–167. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  76. ^ a b Scheibling, R. E. (2014). "Oreaster reticulatus". Starfish: Biology and Ecology of the Asteroidea. Vol. 10. p. 150. Bibcode:2014MBioR..10...93V. doi:10.1080/17451000.2013.820323. in Lawrence (2013)
  77. ^ a b Andersson L, Bohlin L, Iorizzi M, Riccio R, Minale L, Moreno-López W; Bohlin; Iorizzi; Riccio; Minale; Moreno-López (1989). "Biological activity of saponins and saponin-like compounds from starfish and brittle-stars". Toxicon. 27 (2): 179–88. Bibcode:1989Txcn...27..179A. doi:10.1016/0041-0101(89)90131-1. PMID 2718189.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  78. ^ a b Mah, Christopher (20 April 2010). "Sea star defense". The Echinoblog. Retrieved 30 May 2013.
  79. ^ Shedd, John G. (2006). "Crown of Thorns Sea Star". Shedd Aquarium. Archived from the original on 22 February 2014. Retrieved 22 May 2013.
  80. ^ Hewson, Ian; Button, Jason B.; Gudenkauf, Brent M.; Miner, Benjamin; Newton, Alisa L.; Gaydos, Joseph K.; Wynne, Janna; Groves, Cathy L.; et al. (2014). "Densovirus associated with sea-star wasting disease and mass mortality". PNAS. 111 (48): 17278–17283. Bibcode:2014PNAS..11117278H. doi:10.1073/pnas.1416625111. PMC 4260605. PMID 25404293.
  81. ^ Peters, L. E.; Mouchka M. E.; Milston-Clements, R. H.; Momoda, T. S.; Menge, B. A. (2008). "Effects of environmental stress on intertidal mussels and their sea star predators". Oecologia. 156 (3): 671–680. Bibcode:2008Oecol.156..671P. doi:10.1007/s00442-008-1018-x. PMID 18347815. S2CID 19557104.
  82. ^ Pincebourde, S.; Sanford, E.; Helmuth, B. (2008). "Body temperature during low tide alters the feeding performance of a top intertidal predator". Limnology and Oceanography. 53 (4): 1562–1573. Bibcode:2008LimOc..53.1562P. doi:10.4319/lo.2008.53.4.1562. S2CID 1043536.
  83. ^ Pincebourde, S.; Sanford, E.; Helmuth, B. (2009). "An intertidal sea star adjusts thermal inertia to avoid extreme body temperatures". The American Naturalist. 174 (6): 890–897. doi:10.1086/648065. JSTOR 10.1086/648065. PMID 19827942. S2CID 13862880.
  84. ^ Pincebourde, S.; Sanford, E.; Helmuth, B. (2013). "Survival and arm abscission are linked to regional heterothermy in an intertidal sea star". Journal of Experimental Biology. 216 (12): 2183–2191. doi:10.1242/jeb.083881. PMID 23720798. S2CID 4514808.
  85. ^ Newton, L. C.; McKenzie, J. D. (1995). "Echinoderms and oil pollution: A potential stress assay using bacterial symbionts". Marine Pollution Bulletin. 31 (4–12): 453–456. Bibcode:1995MarPB..31..453N. doi:10.1016/0025-326X(95)00168-M.
  86. ^ Temara, A.; Skei, J.M.; Gillan, D.; Warnau, M.; Jangoux, M.; Dubois, Ph. (1998). "Validation of the asteroid Asterias rubens (Echinodermata) as a bioindicator of spatial and temporal trends of Pb, Cd, and Zn contamination in the field". Marine Environmental Research. 45 (4–5): 341–56. Bibcode:1998MarER..45..341T. doi:10.1016/S0141-1136(98)00026-9.
  87. ^ Gooding, Rebecca A.; Harley, Christopher D. G.; Tang, Emily (2009). "Elevated water temperature and carbon dioxide concentration increase the growth of a keystone echinoderm". Proceedings of the National Academy of Sciences. 106 (23): 9316–9321. Bibcode:2009PNAS..106.9316G. doi:10.1073/pnas.0811143106. PMC 2695056. PMID 19470464.
  88. ^ a b Wagonner, Ben (1994). "Echinodermata: Fossil Record". Echinodermata. The Museum of Paleontology of The University of California at Berkeley. Retrieved 31 May 2013.
  89. ^ Benton, Michael J.; Harper, David A. T. (2013). "15. Echinoderms". Introduction to Paleobiology and the Fossil Record. Wiley. ISBN 978-1-118-68540-2.
  90. ^ a b Knott, Emily (2004). "Asteroidea: Sea stars and starfishes". Tree of Life web project. Retrieved 19 October 2012.
  91. ^ a b Mah, Christopher L.; Blake, Daniel B. (2012). Badger, Jonathan H (ed.). "Global diversity and phylogeny of the Asteroidea (Echinodermata)". PLOS ONE. 7 (4): e35644. Bibcode:2012PLoSO...735644M. doi:10.1371/journal.pone.0035644. PMC 3338738. PMID 22563389.
  92. ^ Purit, J. B.; Keever, C. C.; Addison, J. A.; Byrne, M.; Hart, M. W.; Grosberg, R. K.; Toonen, R. J. (2012). "Extraordinarily rapid life-history divergence between Cryptasterina sea star species". Proceedings of the Royal Society B: Biological Sciences. 279 (1744): 3914–3922. doi:10.1098/rspb.2012.1343. PMC 3427584. PMID 22810427.
  93. ^ Hansson, Hans (2013). "Asteroidea". WoRMS. World Register of Marine Species. Retrieved 19 July 2013.
  94. ^ "Etymology of the Latin word Asteroidea". MyEtymology. 2008. Archived from the original on 21 October 2013. Retrieved 19 July 2013.{{cite web}}: CS1 maint: unfit URL (link)
  95. ^ Wray, Gregory A. (1999). "Echinodermata: Spiny-skinned animals: sea urchins, starfish, and their allies". Tree of Life web project. Retrieved 19 October 2012.
  96. ^ Stöhr, S.; O'Hara, T. "World Ophiuroidea Database". Retrieved 19 October 2012.
  97. ^ Mah, Christopher (2012). "Brisingida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  98. ^ Downey, Maureen E. (1986). "Revision of the Atlantic Brisingida (Echinodermata: Asteroidea), with description of a new genus and family" (PDF). Smithsonian Contributions to Zoology (435). Smithsonian Institution Press: 1–57. doi:10.5479/si.00810282.435. Archived from the original (PDF) on 27 February 2012. Retrieved 18 October 2012.
  99. ^ Mah, Christopher. "Brisingida". Access Science: Encyclopedia. McGraw-Hill. Archived from the original on 30 October 2012. Retrieved 15 September 2012.
  100. ^ a b c Vickery, Minako S.; McClintock, James B. (2000). "Comparative morphology of tube feet among the Asteroidea: phylogenetic implications". Integrative and Comparative Biology. 40 (3): 355–364. doi:10.1093/icb/40.3.355.
  101. ^ Mah, Christopher (2012). "Forcipulatida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  102. ^ Barnes, Robert D. (1982). Invertebrate Zoology. Holt-Saunders International. p. 948. ISBN 978-0-03-056747-6.
  103. ^ Mah, Christopher. "Forcipulatida". Access Science: Encyclopedia. McGraw-Hill. Archived from the original on 30 October 2012. Retrieved 15 September 2012.
  104. ^ Mah, Christopher (2012). "Notomyotida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  105. ^ Mah, Christopher (2012). "Paxillosida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  106. ^ Matsubara, M.; Komatsu, M.; Araki, T.; Asakawa, S.; Yokobori, S.-I.; Watanabe, K.; Wada, H. (2005). "The phylogenetic status of Paxillosida (Asteroidea) based on complete mitochondrial DNA sequences". Molecular Genetics and Evolution. 36 (3): 598–605. Bibcode:2005MolPE..36..598M. doi:10.1016/j.ympev.2005.03.018. PMID 15878829.
  107. ^ Mah, Christopher (2012). "Astropecten polyacanthus Müller & Troschel, 1842". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  108. ^ Mah, Christopher (2012). "Spinulosida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  109. ^ "Spinulosida". Access Science: Encyclopedia. McGraw-Hill. Archived from the original on 30 October 2012. Retrieved 15 September 2012.
  110. ^ a b Blake, Daniel B. (1981). "A reassessment of the sea-star orders Valvatida and Spinulosida". Journal of Natural History. 15 (3): 375–394. Bibcode:1981JNatH..15..375B. doi:10.1080/00222938100770291.
  111. ^ Mah, Christopher (2012). "Echinaster (Echinaster) sepositus (Retzius, 1783)". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  112. ^ Mah, Christopher (2012). "Valvatida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  113. ^ Mah, Christopher (2012). "Culcita (Agassiz, 1836)". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  114. ^ Mah, Christopher (2012). "Dermasterias imbricata (Grube, 1857)". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  115. ^ Mah, Christopher (2012). "Xyloplax Baker, Rowe & Clark, 1986". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  116. ^ Mah, Christopher (2012). "Velatida". WoRMS. World Register of Marine Species. Retrieved 15 September 2012.
  117. ^ Mah, Christopher. "Velatida". Access Science: Encyclopedia. McGraw-Hill. Archived from the original on 30 October 2012. Retrieved 15 September 2012.
  118. ^ Mah, Christopher (2012). "Pteraster tesselatus Ives, 1888". WoRMS. World Register of Marine Species. Retrieved 6 July 2013.
  119. ^ "Family Calliasterellidae". Paleobiology Database. Archived from the original on 9 March 2016. Retrieved 10 May 2013.
  120. ^ Walker, Cyril, Ward, DavidFossils : Smithsonian Handbook, ISBN 0-7894-8984-8 (2002, paperback, revisited), ISBN 1-56458-074-1 (1992, 1st edition). Page 186
  121. ^ Telford, M. J.; Lowe, C. J.; Cameron, C. B.; Ortega-Martinez, O.; Aronowicz, J.; Oliveri, P.; Copley, R. R. (2014). "Phylogenomic analysis of echinoderm class relationships supports Asterozoa". Proceedings of the Royal Society B: Biological Sciences. 281 (1786): 20140479. doi:10.1098/rspb.2014.0479. PMC 4046411. PMID 24850925.
  122. ^ Gale, A. S. (1987). "Phylogeny and classification of the Asteroidea (Echinodermata)". Zoological Journal of the Linnean Society. 89 (2): 107–132. doi:10.1111/j.1096-3642.1987.tb00652.x.
  123. ^ Blake, D. B. (1987). "A classification and phylogeny of post-Paleozoic sea stars (Asteroidea: Echinodermata)". Journal of Natural History. 21 (2): 481–528. Bibcode:1987JNatH..21..481B. doi:10.1080/00222938700771141.
  124. ^ Janies, Daniel A.; Voight, Janet R.; Daly, Marymegan (2011). "Echinoderm phylogeny including Xyloplax, a progenetic asteroid". Syst. Biol. 60 (4): 420–438. doi:10.1093/sysbio/syr044. PMID 21525529.
  125. ^ Wessel, G. M.; Reich, A. M.; Klatsky, P. C. (2010). "Use of sea stars to study basic reproductive processes". Systems Biology in Reproductive Medicine. 56 (3): 236–245. doi:10.3109/19396361003674879. PMC 3983664. PMID 20536323.
  126. ^ Lenart Group. "Cytoskeletal dynamics and function in oocytes". European Molecular Biology Laboratory. Archived from the original on 1 August 2014. Retrieved 22 July 2013.
  127. ^ Davydov, P. V.; Shubravyi, O. I.; Vassetzky, S. G. (1990). Animal Species for Developmental Studies: The Starfish Asterina pectinifera. Springer US. pp. 287–311. doi:10.1007/978-1-4613-0503-3. ISBN 978-1-4612-7839-9. S2CID 42046815.
  128. ^ Friedman, Rachel S. C.; Krause, Diane S. (2009). "Regeneration and repair: new findings in stem cell research and ageing". Annals of the New York Academy of Sciences. 1172 (1): 88–94. doi:10.1111/j.1749-6632.2009.04411.x. PMID 19735242. S2CID 755324.
  129. ^ Ted Ranosa (19 June 2015). "Starfish Shows Off Strange Ability To Expel Foreign Objects Through Skin". Tech Times, Science. Archived from the original on 1 January 2016.
  130. ^ "William Jenkyn Thomas, M.A". The Aberdare Boys' Grammar School. Archived from the original on 6 June 2014. Retrieved 12 May 2013.
  131. ^ Thomas, William Jenkyn (1943). Some Myths and Legends of the Australian Aborigines. Whitcombe & Tombs. pp. 21–28.
  132. ^ Tregear, Edward (1900). ""The Creation Song" of Hawaii". The Journal of the Polynesian Society. 9 (1): 38–46. Archived from the original on 12 February 2016. Retrieved 13 May 2013.
  133. ^ a b Rumphius, Georgious Everhardus (= Georg Eberhard Rumpf); Beekman, E.M. (trans.) (1999) [1705]. The Ambonese Curiosity Cabinet (original title: Amboinsche Rariteitkamer). Yale University Press. p. 68. ISBN 978-0-300-07534-2.{{cite book}}: CS1 maint: multiple names: authors list (link)
  134. ^ Watts, Peter (2008). Starfish (Rifters Trilogy). Tor. ISBN 978-0-7653-1596-0.
  135. ^ Orbell, Jennie (2012). Starfish. Tedge Press. ISBN 978-1-5147-8841-7.
  136. ^ Addison, Alice (2012). Starfish: A Year in the Life of Bereavement and Depression. Chipmunkapublishing. ISBN 978-1-8499-1995-1.
  137. ^ Brafman, Ori; Beckstrom, Rod (2006). The Starfish and the Spider: The Unstoppable Power of Leaderless Organizations. Penguin. ISBN 978-1-59184-183-8.
  138. ^ "SpongeBob SquarePants". Patrick. Nickelodeon. 2013. Archived from the original on 7 October 2014. Retrieved 16 May 2013.
  139. ^ Lin SJ, Hwang DF; Hwang (April 2001). "Possible source of tetrodotoxin in the starfish Astropecten scoparius". Toxicon. 39 (4): 573–9. Bibcode:2001Txcn...39..573L. doi:10.1016/S0041-0101(00)00171-9. PMID 11024497.
  140. ^ Asakawa, M.; Nishimura, F.; Miyazawa, K.; Noguchi, T. (1997). "Occurrence of paralytic shellfish poison in the starfish Asterias amurensis in Kure Bay, Hiroshima Prefecture, Japan". Toxicon. 35 (7): 1081–1087. Bibcode:1997Txcn...35.1081A. doi:10.1016/S0041-0101(96)00216-4. PMID 9248006.
  141. ^ "Indulging in Exotic Cuisine in Beijing". The China Guide. 2011. Archived from the original on 3 March 2014. Retrieved 28 February 2014.
  142. ^ Amakusa TV Co. Ltd. (7 August 2011). "Cooking Starfish in Japan". ebook10005. Amakusa TV. Retrieved 18 May 2013.
  143. ^ "Pouch A" (in Japanese). Kenko.com. Archived from the original on 3 August 2014. Retrieved 18 May 2013.
  144. ^ Johannes, Robert Earle (1981). Words of the Lagoon: Fishing and Marine Lore in the Palau District of Micronesia. University of California Press. pp. 87.
  145. ^ Bos, A. R.; Gumanao, G. S.; Alipoyo, J. C. E.; Cardona, L. T. (2008). "Population dynamics, reproduction and growth of the Indo-Pacific horned sea star, Protoreaster nodosus (Echinodermata; Asteroidea)". Marine Biology. 156 (1): 55–63. Bibcode:2008MarBi.156...55B. doi:10.1007/s00227-008-1064-2. hdl:2066/72067. S2CID 84521816.
  146. ^ "Starfish". Larva Labs. Archived from the original on 28 July 2014. Retrieved 10 May 2013.
  147. ^ Starfish Associates LLC (2005–2013). "Starfish". Starfish Associates. Retrieved 10 May 2013.
  148. ^ "Motorola to Acquire Starfish". Motorola. 14 July 1998. Archived from the original on 7 February 2012. Retrieved 11 May 2013. (See also Starfish Software.)
  149. ^ "Starfish". Duke Startup Challenge. Duke University. Archived from the original on 7 March 2013. Retrieved 10 May 2013.
  150. ^ "Starfish". Starfish Seabed Imaging Systems. 2013. Archived from the original on 20 January 2012. Retrieved 10 May 2013.
  151. ^ Manning, T. D. (Captain) (1961). The British Destroyer. Godfrey Cave Associates. ISBN 978-0-906223-13-0.
  152. ^ "Admiralty R-class destroyers (1915–1917)". Royal Navy History. Archived from the original on 3 December 2013. Retrieved 12 July 2013.
  153. ^ "HM Submarine Starfish". Submarines: Chatham built. 1 July 2013. Archived from the original on 7 September 2013. Retrieved 13 July 2013.
  154. ^ Crowdy, Terry (2008). Deceiving Hitler: double cross and deception in World War II. Osprey Publishing. p. 61. ISBN 978-1-84603-135-9.
  155. ^ Dyal, P. (10 December 1965). "Operation Dominic, Fish Bowl Series, Project Officer's Report; Project 6.7: Debris Expansion Experiment, Extracted Version" (PDF). Air Force Weapons Laboratory. Report AD-A995 428. Archived (PDF) from the original on 5 November 2010. Retrieved 11 May 2013.

Bibliography

  • Lawrence, J. M., ed. (2013). Starfish: Biology and Ecology of the Asteroidea. Johns Hopkins University Press. ISBN 978-1-4214-0787-6.
  • Ruppert, Edward E.; Fox, Richard S.; Barnes, Robert D. (2004). Invertebrate Zoology (7th ed.). Cengage Learning. ISBN 978-81-315-0104-7.
Wikimedia Commons has media related to Starfish.
  • Mah, Christopher L. (24 January 2012). "The Echinoblog". A blog about sea stars by a passionate and professional specialist.
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