Diversity of fish

Fish are very diverse animals and can be categorised in many ways. This article is an overview of some of ways in which fish are categorised. Although most fish species have probably been discovered and described, about 250 new ones are still discovered every year. According to FishBase about 34,800 species of fish had been described as of February 2022,^[5] which is more than the combined total of all other vertebrate species: mammals, amphibians, reptiles and birds.

Fish come in many shapes and sizes. This is a sea dragon, a close relative of the seahorse. They are camouflaged to look like floating seaweed.^[1][2][3]

The deep sea Lasiognathus amphirhamphus is a rare ambush predator known only from a single female specimen (pictured).^[4] It is an angler fish that "angles" for its prey with a lure attached to a line from its head.

Fish species diversity is roughly divided equally between marine (oceanic) and freshwater ecosystems. Coral reefs in the Indo-Pacific constitute the centre of diversity for marine fishes, whereas continental freshwater fishes are most diverse in large river basins of tropical rainforests, especially the Amazon, Congo, and Mekong basins. More than 5,600 fish species inhabit Neotropical freshwaters alone, such that Neotropical fishes represent about 10% of all vertebrate species on the Earth. Exceptionally rich sites in the Amazon basin, such as Cantão State Park, can contain more freshwater fish species than occur in all of Europe.^[6]

By taxonomy

fishes      jawless lampreys   hagfish      cartilaginous    sharks   rays   chimaera   bony lobe finned lungfish   coelacanths   ray finned chondrosteans   holosteans   teleosts

Basic taxonomy of fishes

Fish systematics is the formal description and organisation of fish taxa into systems. It is complex and still evolving. Controversies over "arcane, but important, details of classification are still quietly raging".^[7]

The term "fish" describes any non-tetrapod chordate, (i.e., an animal with a backbone), that has gills throughout life and has limbs, if any, in the shape of fins.^[8] Unlike groupings such as birds or mammals, fish are not a single clade but a paraphyletic collection of taxa, including jawless, cartilaginous and skeletal types.^[9][10]

Jawless fish

Jawless fish were the earliest fish to evolve. There is current debate over whether these are really fish at all. They have no jaw, no scales, no paired fins, and no bony skeleton. Their skin is smooth and soft to the touch, and they are very flexible. Instead of a jaw, they possess an oral sucker. They use this to fasten onto other fish, and then use their rasp-like teeth to grind through their host's skin into the viscera. Jawless fish inhabit both fresh and salt water environments. Some are anadromous, moving between both fresh and salt water habitats.

Extant jawless fish are either lamprey or hagfish. Juvenile lamprey feed by sucking up mud containing micro-organisms and organic debris. The lamprey has well-developed eyes, while the hagfish has only primitive eyespots. The hagfish coats itself and carcasses it finds with noxious slime to deter predators, and periodically ties itself into a knot to scrape the slime off. It is the only invertebrate fish and the only animal which has a skull but no vertebral column.^[11]

•  

  Lampreys attached to a lake trout

•  

  Mouth of a sea lamprey

•  

  Pacific hagfish resting on bottom at 280 m

Cartilaginous fish

Cartilaginous fish have a cartilaginous skeleton. However, their ancestors were bony animals, and were the first fish to develop paired fins. Cartilaginous fish don't have swim bladders. Their skin is covered in placoid scales (dermal denticles) that are as rough as sandpaper. Because cartilaginous fish do not have bone marrow, the spleen and special tissue around the gonads produces red blood cells. Their tails can be asymmetric, with the upper lobe longer than the lower lobe. Some cartilaginous fishes possess an organ called a Leydig's organ which also produces red blood cells.

There are over 980 species of cartilaginous fish. They include sharks, rays and chimaera.

•  

  Tiger shark

•  

  Whale shark

•  

  Stingray

•  

  This elephant fish is a chimaera

Bony fish

Bony fish include the lobe-finned fish and the ray finned fish. The lobe-finned fish is the class of fleshy finned fishes, consisting of lungfish and coelacanths. They are bony fish with fleshy, lobed paired fins, which are joined to the body by a single bone.^[12] These fins evolved into the legs of the first tetrapod land vertebrates, amphibians. Ray finned fishes are so-called because they possess lepidotrichia or "fin rays", their fins being webs of skin supported by bony or horny spines ("rays").

There are three types of ray finned fishes: the chondrosteans, holosteans, and teleosts. The chondrosteans and holosteans are among the earlier fish to evolve, and share characteristics with both teleosts and sharks. In comparison with the other chondrosteans, the holosteans are closer to the teleosts and further from sharks.

•  

  Lungfish can breathe in air as well as water

•  

  Model of a coelacanth, thought until 1938 to be extinct. They are deep blue.

•  

  This Atlantic sturgeon is a chondrostean

•  

  This bowfin is a holostean

Teleosts

Teleosts are the most advanced or "modern" fishes. They are overwhelmingly the dominant class of fishes (or for that matter, vertebrates) with nearly 30,000 species, covering about 96 percent of all extant fish species. They are ubiquitous throughout fresh water and marine environments from the deep sea to the highest mountain streams. Included are nearly all the important commercial and recreational fishes.^[13]

Teleosts have a movable maxilla and premaxilla and corresponding modifications in the jaw musculature. These modifications make it possible for teleosts to protrude their jaws outwards from the mouth.^[14][15] The caudal fin is homocercal, meaning the upper and lower lobes are about equal in size. The spine ends at the caudal peduncle, distinguishing this group from those in which the spine extends into the upper lobe of the caudal fin.^[14]

•  

  Swordfish are teleosts

•  

  Rose fish are also teleosts

•  

  Eels are teleosts too

•  

  So are seahorses

By habitat

See also: Marine habitats There is 10,000 times as much saltwater in the oceans as there is freshwater in the lakes and rivers. However, only 58 percent of extant fish species live in saltwater. A disproportionate 41 percent are freshwater fish (the remaining one percent are anadromous).^[16] This diversity in freshwater species is perhaps not surprising, since the thousands of separate lake habitats promote speciation.^[17] Habitat Area Volume Depth Species Fish biomass million km^2 million cu km (mean) count percent million tonnes Saltwater 361^[18] 1370.8^[19] 3.8 km 18,000 58^[16] 800-2,000^[20] Freshwater 1.5^[21] 0.13^[22] 87 m 13,000 41^[16] Fish can also be demersal or pelagic. Demersal fish live on or near the bottom of oceans and lakes, while pelagic fish inhabit the water column away from the bottom. Habitats can also be vertically stratified. Epipelagic fish occupy sunlit waters down to 200 metres (110 fathoms), mesopelagic fish occupying deeper twilight waters down to 1,000 meters (3,300 ft), and bathypelagic fish inhabiting the cold and pitch black depths below. Most oceanic species (78 percent, or 44 percent of all fish species), live near the shoreline. These coastal fish live on or above the relatively shallow continental shelf. Only 13 percent of all fish species live in the open ocean, off the shelf. Of these, 1 percent are epipelagic, 5 percent are pelagic, and 7 percent are deep water.^[16] Fish are found in nearly all natural aquatic environments.^[23] Most fish, whether by species count or abundance, live in warmer environments with relatively stable temperatures.^[17] However, some species survive temperatures up to 44.6 °C (112.3 °F), while others cope with colder waters; there are over 200 finfish species south of the Antarctic Convergence.^[24] Some fish species tolerate salinities over 10 percent.^[23]

Habitat	Abyssobrotula galatheae		The world's deepest living fish, Abyssobrotula galatheae, a species of cusk eel, lives in the Puerto Rico Trench at a depth of 8,372 meters (27,467 ft).^[23]^[25] Due to the extreme pressure, this appears to be around the theoretical maximum depth possible for fish.^[26]^[27]
	Stone loach		At the other extreme, the Tibetan stone loach lives at altitudes over 5,200 meters (17,100 ft) in the Himalayas.^[23]^[28]
	Blue shark		Some marine pelagic fish range over vast areas, such as the blue shark that lives in all oceans.
	Blind cave fish		Other fish are confined to single, small living spaces, such as the blind cave fish in North America.^[29]
	Death Valley pupfish		Equally isolated desert pupfish, like the Death Valley pupfish (pictured), live in small desert spring systems in Mexico and the southwest United States.
	Thermichthys hollisi		The bythitid vent fish Thermichthys hollisi lives around thermal vents 2,400 metres (1,300 fathoms) deep.^[23]^[30]
	Sargassum frogfish		The highly camouflaged sargassum frogfish lives in drifting sargassum seaweed. It has adapted fins which can grab strands of sargassum, enabling it to climb through the seaweed.^[31] It avoids threats from larger predator fish by climbing out of water onto the surface of a seaweed mat, where it can survive for some time.^[32]

By life span

Some of the shortest-lived species are gobies, which are small coral reef–dwelling fish. Some of the longest-lived are rockfish.

Life span	Seven-figure pygmy goby		External image   World's shortest lived fish Gobies, a type of small coral reef-dwelling fish (pictured), are some of the shortest lived fishes. The seven-figure pygmy goby is the shortest lived of all fish species. It lives at most for 59 days, which is the shortest lifespan for any vertebrate.^[33]
	Ram cichlid		Short lived fish have particular value in genetic studies on aging. In particular, the ram cichlid is used in laboratory studies because of its ease of breeding and predictable aging pattern.^[34]^[35]
	Rougheye rockfish		Some of the longest living fishes are rockfish. The longest lived fish is the 205 years reported for the rougheye rockfish, Sebastes aleutianus (pictured). This fish is found offshore in the North Pacific at 25–900 metres (14–492 fathoms) and exhibits negligible senescence.^[36]^[37]^[38]
	Orange roughy		The orange roughy may be the longest lived commercial fish, with a maximum reported age of 149 years.^[39]
	Koi		There are stories about Japanese koi goldfish passed from generation to generation for 300 years. Scientists are sceptical. Counting growth lines on the scales of fish confined to ponds or bowls is unreliable, since they lay down extra lines.^[40]^[41] The maximum reliably reported age for a goldfish is 41 years.^[42]
	Atlantic tarpon		One of the longest living sport fish is the Atlantic tarpon, with a reported age of 55 years.^[43]^[44]^[45]
	Green sturgeon		Some of the longest living fish are living fossils, such as the green sturgeon. This species is among the longest living species found in freshwater, with a reported age of 60 years. They are also among the largest fish species found in freshwater, with a maximum reported length of 2.5 meters (8.2 ft) and a maximum reported weight of 159 kg (351 lb).^[46]^[47]^[48]
	Australian lungfish		Another living fossil is the Australian lungfish. One individual has lived in an aquarium for at least 75 years, and is the oldest fish in captivity. According to fossil records, the Australian lungfish has hardly changed for 380 million years.^[49]^[50]^[51]
	Greenland shark		The Greenland shark has a lifespan of 392 ± 120 years. This is the longest known lifespan of all vertebrate species.^[52]

By size

Size	Paedocypris progenetica		External image   World's smallest fish Paedocypris progenetica, a type of minnow, is the smallest of all fish species. It lives in the dark-colored peat swamps of the Indonesian island of Sumatra. The females of this species have a standard length of 7.9 mm (0.31 in) at maturity.^[53]^[54]^[55] Until recently, this was the smallest of all known vertebrates. However, in 2012 a minute Papua New Guinea frog, Paedophryne amauensis, with a standard length of 7.7 mm (0.30 in) was discovered.^[56] The slender Indonesian fish may still be the smallest vertebrate by weight.
	Photocorynus spiniceps		Male individuals of the anglerfish species Photocorynus spiniceps are 6.2–7.3 mm (0.24–0.29 in) long at maturity, and thus could be claimed as an even smaller species. However, these males do not survive on their own merit, only by sexual parasitism on the larger female.^[57]^[58]^[59]^[60]
	Stout infantfish		The stout infantfish, a type of goby, is the second smallest known fish.^[61] Females grow to a length of 8.4 millimetres (0.33 in) and males are mature at 7 millimetres (0.28 in).
	Sinarapan		According to the Guinness Book of World Records, the sinarapan, also a goby, is the world's smallest commercially harvested fish.^[62] Found in the Philippines, they have an average length of 12.5 mm (0.49 in), and are threatened by overfishing.^[55]
	Whale shark		The largest fish is the whale shark. It is a slow-moving, filter-feeding shark with a maximum published length of 20 m (66 ft) and a maximum weight of 34 tonnes (33 long tons; 37 short tons). Whale sharks can live up to 70 years^[63] and are a vulnerable fish.
	Ocean sunfish		The ocean sunfish is the heaviest bony fish. It can weigh up to 2,300 kg (5,100 lb). It is found in all warm and temperate oceans.^[64]
	King of herrings		The king of herrings is the longest bony fish. Its total length can reach 11 m (36 ft), and it can weigh up to 272 kilograms (600 lb). It is a rarely seen oarfish, found in all the world's oceans at depths of between 20 m (66 ft) and 1,000 m (3,300 ft).^[65]
	Mekong giant catfish		The largest recorded freshwater fish is a Mekong giant catfish caught in 2010, weighing 293 kg (646 lb).^[66]^[67] The Mekong giant catfish is critically endangered.

By breeding behavior

See also: Spawning and Ichthyoplankton In very deep waters, it is not easy for a fish to find a mate. There is no light, so some species depend on bioluminescence. Others are hermaphrodites, which doubles their chances of producing both eggs and sperm when an encounter does occur.^[68]

Breeding	Grouper		Female groupers change their sex to male if no male is available. Grouper are protogynous hermaphrodites, who school in harems of three to fifteen females. When no male is available, the most aggressive and largest females change their sex to male.
	Toadfish		Male toadfish "sing" at up to 100 decibels with their swim bladders to attract mates.^[69]^[70]^[71]
	Anglerfish		Female Haplophryne mollis anglerfish trailing atrophied males she encountered (pictured).^[72] The female anglerfish releases pheromones to attract tiny males. When a male finds her, he bites on to her and holds on. When a male of the anglerfish species Haplophryne mollis bites into the skin of a female, he releases an enzyme that digests the skin of his mouth and her body, fusing the pair to the point where the two circulatory systems join up. The male then atrophies into nothing more than a pair of gonads. This extreme sexual dimorphism ensures that, when the female is ready to spawn, she has a mate immediately available.^[73]
	Hammerheads		Some sharks such as hammerheads^[74] are able to breed parthenogenetically, a type of asexual reproduction where the growth and development of embryos occur without fertilization.

By brooding behavior

See also: Spawning Fish adopt a variety of strategies for nurturing their brood. Sharks, for example, variously follow three protocols with their brood. Most sharks, including lamniformes,^[75] are ovoviviparous, bearing their young after the brood nourish themselves, both after hatching and before birth, by consuming the remnants of the yolk and other available nutrients. Some, such as hammerheads,^[74] are viviparous, bearing their young after nourishing hatchlings internally, analogously to mammalian gestation. Catsharks^[76] and others are oviparous, laying their eggs to hatch in the water. Some animals, predominantly fish such as cardinalfish,^[77] practice mouthbrooding, caring for their offspring by holding them in the mouth of a parent for extended periods of time. Mouthbrooding has evolved independently in several different families of fish.

Brooding	Chain catshark		The chain catshark is oviparous, laying its eggs to hatch in the water.
	Great white shark		The great white shark is ovoviviparous, gestating eggs in the uterus for 11 months before giving birth.
	Scalloped hammerhead		The scalloped hammerhead is viviparous, bearing its young after nourishing hatchlings internally.
	Cyphotilapia frontosa		The female Cyphotilapia frontosa mouthbroods its fry. The fry can be seen looking out of her mouth.
	Seahorses		Seahorse males practice pouch-brooding similar to kangaroos. When seahorses mate, the female deposits her eggs into a special pouch on the male's belly. The pouch seals shut while he nurtures the developing eggs. Once the eggs hatch, the pouch opens and the male goes into labour.^[78]

By feeding behaviour

External images   Video of a slingjaw wrasse catching prey by protruding its jaw   Video of a red bay snook catching prey by suction feeding Further information: Aquatic feeding mechanisms There are three basic methods by which food is gathered into the mouths of fish: by suction feeding, by ram feeding, and by manipulation or biting.^[79] Nearly all fish species use one of these styles, and most use two.^[80] Early fish lineages had inflexible jaws limited to little more than opening and closing. Modern teleosts have evolved protusible jaws that can reach out to engulf prey.^[81]^[82] An extreme example is the protusible jaw of the slingjaw wrasse. Its mouth extends into a tube half as long as its body, which creates a strong suction to catch prey. The extended mouth tucks away under its body when not in use.^[83]^[84] In practice, feeding modes lie on a spectrum, with suction and ram feeding at the extremes. Many fish capture their prey using both suction pressure combined with a forward motion of the body or jaw.^[85] Most fish are food opportunists, or generalists. They eat whatever is most easily available.^[86] For example, the blue shark feeds on dead whales and nearly everything else that wriggles: other fish, cephalopods, gastropods, ascidians, or crustaceans.^[87]^[88] Ocean sunfish prefer jellyfish.^[64]

Feeding	Anglerfish		Anglerfish are lie-in-wait ambush predators. The first spine of their dorsal fin has been modified so it can be used like a fishing line with a lure at the end. Most anglerfish, like the one pictured, live in the darkness of the deep sea and have a bioluminescent lure.^[89]
	Archerfish		Archerfish prey on land-based insects and other small animals by shooting them down with water droplets from their specialized mouths. Archerfish are remarkably accurate; adults almost always hit the target on the first shot. They can bring down arthropods such as grasshoppers,^[90] spiders and butterflies on a branch of an overhanging tree^[91] 3 m (9.8 ft) above the water's surface.^[92] This is partially due to good eyesight, but also due to their ability to compensate for light refraction when aiming.^[93]
	Triggerfish		Triggerfish also use jets of water to uncover sand dollars buried in sand or overturn sea urchins.^[94]
	Silver arowana		Other fish have developed extreme specializations. Silver arowana, also called monkey fish, can leap two meters out of the water to capture prey. They usually swim near the surface of the water waiting for potential prey. Their main diet consists of crustaceans, insects, smaller fishes and other animals that float on the water surface, for which its draw-bridge-like mouth is exclusively adapted for feeding. The remains of small birds, bats, and snakes have also been found in their stomachs.^[95]
	Cookiecutter shark		The cookiecutter shark is a small dogfish which derives its name from the way it removes small circular plugs, looking as though cut with a cookie cutter, from the flesh and skin of cetaceans and larger fish, including other sharks. The cookiecutter attaches to its larger prey with its suctorial lips, and then protrudes its teeth to remove a symmetrical scoop of flesh.^[96] Pictured is a pomfret with bite wounds from a cookiecutter shark.
	Striped bass		Striped bass eat smaller fish.
	Chinese algae eater		Chinese algae eaters are kept in aquaria to control algae.
	Emperor angelfish		The Emperor angelfish feeds on coral sponges.
	Herring		Schooling herrings ram feed on copepods.
	Mangrove jack		The mangrove jack eats crustaceans.
	Puffer fish		Many puffer fish species crush the shells of molluscs.
	Bucktoothed tetra		The bucktoothed tetra eats scales off other fishes (lepidophagy) and molluscs.
	Cleaner fish		These two small wrasses are cleaner fish, which eat parasites off other fish.
	Cleaning station		A reef manta ray at a cleaning station, maintaining a near stationary position atop a coral patch for several minutes while being cleaned by cleaner fishes.^[97]
	Doctor fish		Doctor fish nibbling on the diseased skin of patients. Doctor fish (nibble fish) live and breed in the outdoor pools of some Turkish spas, where they feed on the skin of patients with psoriasis. The fish are like cleaner fish in that they only consume the affected and dead areas of the skin, leaving the healthy skin to recover.

By vision

Main article: Vision in fishes Many species of fish can see the ultraviolet end of the spectrum, beyond the violet wavelength of visible light.^[98] Mesopelagic fishes live in the deeper waters of the twilight zone, down to depths of 1000 metres, where the amount of sunlight available is not sufficient to support photosynthesis. These fish are adapted for an active life under low light conditions.

Vision	Four-eyed fish		The four-eyed fish feeds at the surface of the water with eyes that allow it to see above and below the surface at the same time. Four-eyed fish have two specially-adapted eyes which are raised above the top of their head. The eyes are divided in two different parts, and the fish floats at the water surface with only the lower half of each eye underwater. The two halves are divided by a band of tissue and the eye has two pupils, connected by part of the iris. The upper half of the eye is adapted for vision in air, while the lower half is adapted for vision in water.^[99] The lens of the eye also changes in thickness top to bottom to account for the difference in the refractive indices of air versus water. Their diet mostly consists of the terrestrial insects which are available at the surface, where they spend most of their time.^[100]
	Two stripe damselfish		The two stripe damselfish, Dascyllus reticulatus, has ultraviolet-reflecting colouration which they appear to use as an alarm signal to other fish of their species.^[101] Predatory species cannot see this if their vision is not sensitive to ultraviolet. There is further evidence for this view that some fish use ultraviolet as a "high-fidelity secret communication channel hidden from predators", while yet other species use ultraviolet to make social or sexual signals.^[102]^[103]
	Barreleye		Barreleyes are a family of small, unusual-looking mesopelagic fishes, named for their barrel-shaped, tubular, telescopic eyes which are generally directed upwards to detect the silhouettes of available prey.^[104]^[105] The eyes, which dominate and protrude from the skull, may be swivelled forwards in some species. Their eyes have a large lens and a retina with an exceptional number of rod cells and a high density of rhodopsin (the "visual purple" pigment); there are no cone cells.^[104] The barreleye species Macropinna microstoma has a transparent protective dome over the top of its head, somewhat like the dome over an airplane cockpit, through which the lenses of its eyes can be seen. The dome is tough and flexible, and presumably protects the eyes from the nematocysts (stinging cells) of the siphonophores from which it is believed the barreleye steals food.^[104]^[105]^[106]
	Flashlight fish		Flashlight fish use a retroreflector behind the retina and photophores to detect eyeshine in other fish.^[107]^[108]^[109]

By shape

Boxfishes have heavily armoured plate-like scales fused into a solid, triangular, boxlike carapace, from which the fins, tail, eyes and mouth protrude. Because of this heavy armour, boxfish move slowly, but few other fish are able to eat the adults.^[110]

•  

  The humpback turretfish is a boxfish with an armoured triangular shaped body

•  

  The leafy sea dragon is camouflaged to look like floating seaweed

By locomotion

See also: Fish locomotion A number of species jump while swimming near the surface, skimming the water. Other species walk along the bottom on their fins.

Loco- motion	Dwarf seahorse		The slowest-moving fishes are the sea horses. The slowest of these, the tiny dwarf seahorse, has a sprint speed of one inch per minute.^[111]
	Atlantic bluefin tuna		The Atlantic bluefin tuna is capable of sustained high speed cruising, and maintains high muscle temperatures so it can cruise in relatively cold waters.
	Indo-Pacific sailfish		Among the fastesr sprinters are the Indo-Pacific sailfish (left) and the black marlin (right). Both have been recorded in a burst at over 110 kilometres per hour (68 mph). For the sailfish, that is equivalent to 12 to 15 times their own length per second.
	Shortfin mako		External video   What makes mako sharks fast? National Geographic The shortfin mako shark is fast and agile enough to chase down and kill an adult swordfish. However, sometimes in the struggle the swordfish kills the shark by ramming it in the gills or belly. The shortfin mako's speed has been recorded at 50 kilometres per hour (31 mph), and there are reports that it can achieve bursts of up to 74 kilometres per hour (46 mph).^[112] It can jump up to 9 meters (30 ft) in the air. Due to its speed and agility, this high-leaping fish is sought as game worldwide. This shark is highly migratory. Its exothermic constitution partly accounts for its relatively great speed.^[113]
	Wahoo		The wahoo is perhaps the fastest fish for its size, attaining a speed of 19 lengths per second, reaching 78 kilometres per hour (48 mph).
	Flying fish		Flying fish have unusually large pectoral fins, which enable the fish to take short gliding flights above the surface of the water in order to escape from predators. Their glides are typically around 50 meters (160 ft), but they can use updrafts at the leading edge of waves to cover distances of at least 400 meters (1,300 ft).^[114] In May 2008, a flying fish was filmed off the coast of Japan (see video). The fish spent 45 seconds aloft, and was able to stay aloft by occasionally beating the surface of the water with its caudal (tail) fin.^[115] The previous record was 42 seconds.^[115]
	Climbing perches		Climbing perches are a family of fishes which have the ability to climb out of water and "walk" short distances. As labyrinth fishes, they possess a labyrinth organ, a structure in the fish's head which allows it to breathe atmospheric oxygen. Their method of terrestrial locomotion uses the gill plates as supports, and the fish pushes itself using its fins and tail.
	Mudskipper		External video   Mudskippers: The Fish That Walk on Land BBC Earth The mudskipper is another type of walking fish. Walking fish are often amphibious and can travel over land for extended periods of time. These fish may use a number of means of locomotion, including springing, snake-like lateral undulation, and tripod-like walking. The mudskipper is able to spend days moving about out of water and can even climb mangroves, although to only modest heights.^[116] There are some species of fish that can "walk" along the sea floor but not on land. One such animal is the flying gurnard.
	Handfish		External video   Fish that walk CSIRO The handfish walks along the seafloor using its pectoral fins, which look like hands.
	Tripod fish		External video   Fish that perch Okeanos Explorer ROV Deepsea tripod fishes use their very elongate pelvic fins and caudal fin, which act like "stilts", to perch and walk on the seafloor.

By toxicity

Toxic fish produce strong poisons in their bodies. Both poisonous fish and venomous fish contain toxins, but deliver them differently. Venomous fish bite, sting, or stab, causing an envenomation. Venomous fish don't necessarily cause poisoning if they are eaten, since the digestive system often destroys the venom.^[117] By contrast, poisonous fish do not bite, sting, or stab to deliver their toxins, but they are poisonous to eat because they contain toxins in their body that the digestive system does not destroy.^[117] A 2006 study found that there are at least 1200 species of venomous fish.^[118] There are more venomous fish than venomous snakes. In fact, there are more venomous fish than the combined total of all other venomous vertebrates.^[118] Venomous fish are found in almost all habitats around the world, but mostly in tropical waters. They wound over 50,000 people every year.^[119] Venomous fish carry their venom in venom glands and use various delivery systems, such as spines, sharp fins, barbs, spikes or fangs. Venomous fish tend to be either very visible, using flamboyant colors to warn enemies, or skilfully camouflaged and may be buried in the sand. Apart from the defense or hunting value, venom helps bottom-dwelling fish by killing the bacteria that tries to invade their skin. Few of these venoms have been studied. They are a yet-to-be-tapped resource for bioprospecting to find drugs with medical uses.^[120] Treatment for venom stings usually includes the application of heat, using water at temperatures of about 45 °C (113 °F), since heat breaks down most complex venom proteins.

Toxicity	Puffer fish		The puffer fish is the most poisonous fish in the world. It is the second most poisonous vertebrate after the golden dart frog. It paralyzes the diaphragm muscles of human victims, who can die from suffocation. In Japan, skilled chefs use parts of a closely related species, the blowfish, to create a delicacy called "fugu", including just enough toxin for that "special flavour".^[citation needed]
	Spotted trunkfish		The spotted trunkfish, a reef fish, secretes a colourless ciguatera toxin from glands on its skin when touched. The toxin is only dangerous when ingested, so the fish poses no immediate risk to human divers. However, predators as large as nurse sharks can die from eating a trunkfish.^[121]
	Giant moray		The giant moray is a reef fish at the top of the food chain. Like many other apex reef fish, it is likely to cause ciguatera poisoning if eaten.^[122]^[123] Outbreaks of ciguatera poisoning in the 11th to 15th centuries from large, carnivorous reef fish, caused by harmful algal blooms, could be a reason why Polynesians migrated to Easter Island, New Zealand, and possibly Hawaii.^[124]^[125]
	Reef stonefish		The most venomous known fish is the reef stonefish.^[126]^[127] It has a remarkable ability to camouflage itself amongst rocks. It is an ambush predator that sits on the bottom waiting for prey to approach. Instead of swimming away if disturbed, it erects the 13 venomous spines along its back. For defense, it can shoot venom from each or all of these spines. Each spine is like a hypodermic needle, delivering the venom from two sacs attached to the spine. The stonefish has control over whether to shoot its venom, and does so when provoked or frightened.^[120] The venom results in severe pain, paralysis and tissue death, and can be fatal if not treated. Despite its formidable defenses, stonefish have predators. Some bottom feeding rays and sharks with crushing teeth feed on them, as does the Stokes's sea snake.^[128]
	Lionfish		Head on view of the lionfish, a venomous coral reef fish (pictured).^[129] Unlike stonefish, a lionfish can release venom only if something strikes its spines. Although not native to the U.S. coast, lionfish have appeared around Florida and have spread up the coast to New York. They are attractive aquarium fish, sometimes used to stock ponds, and may have been washed into the sea during a hurricane. Lionfish can aggressively dart at scuba divers and attempt to puncture their facemask with their venomous spines.^[120]
	Stargazer		The stargazer, Uranoscopus sulphureus.^[130] The stargazer buries itself and can deliver electric shocks as well as venom. It is a delicacy in some cultures (cooking destroys the venom), and can be found for sale in some fish markets with the electric organ removed. They have been called "the meanest things in creation".^[120]
	Stingray		Stingrays can sting with their stinger (pictured). Such envenomations can occur to people who wade in shallow water and tread on them. This can be avoided by shuffling through the sand or stamping on the bottom, as the rays detect this and swim away. The stinger usually breaks off in the wound. It is barbed, so it can easily penetrate but cannot be easily removed. The stinger causes local trauma from the cut itself, pain and swelling from the venom, and possible later infection from bacteria. Occasionally, severed arteries or death can result.^[131]

By human use

Predator fish size up schooling forage fish Fish are sought after by humans for their value as commercial food fish, recreational sport fish, decorative aquarium fish and for tourism, as they attract snorkelers and scuba divers. Throughout human history, important fisheries have been based on forage fish.^[132] Forage fish are small fish which are eaten by larger predators. They usually school together for protection. Typical ocean forage fish feed near the bottom of the food chain on plankton, often by filter feeding. They include the family Clupeidae (herrings, sardines, menhaden, hilsa, shad and sprats), as well as anchovies, capelin and halfbeaks. Important herring fisheries have existed for centuries in the North Atlantic and the North Sea. Likewise, important traditional for anchovy and sardine fisheries have operated in the Pacific, the Mediterranean, and the southeast Atlantic.^[133] The world annual catch of forage fish in recent years has been around 25 million tonnes, or one quarter of the world's total catch. Higher in the food chain, Gadidae (cod, pollock, haddock, saithe, hake and whiting) also support important fisheries. Concentrated initially in the North Sea, Atlantic cod was one of Europe's oldest fisheries, later extending to the Grand Banks.^[134] Declining numbers led to international "cod wars" and eventually the virtual abandonment of these fisheries. In modern times, the Alaska pollock supports an important fishery in the Bering Sea and the north Pacific, yielding about 6 million tonnes, while cod amounts to about 9 million tonnes.^[133] Food fish, Oily fish, whitefish Farmed fish fish used for medicinal purposes Recreational and sport fishing is big business^[135] U.S. saltwater fishers spend about $30 billion annually and support 350,000 jobs.^[136] Some of the more popular recreational and sport fish include bass, marlin, porgie, shad, mahi-mahi, smelt whiting, swordfish, and walleye. Fishkeeping is another popular pastime, and there is a large international trade for aquarium fish. Snorkeling and scuba diving attracts millions of people to beaches, coral reefs, lakes, and other bodies of water to view fish and other marine life.

Human use	Yellowfin tuna		Yellowfin tuna are now being fished as a replacement for the depleted southern bluefin tuna.
	Anchovy		These schooling anchovy are forage fish.
	Atlantic cod		Atlantic cod fisheries have collapsed.
	Alaska pollock		The Alaska pollock has been described as "the largest remaining source of palatable fish in the world".^[137]
	Koi		Koi (and goldfish) have been kept in decorative ponds for centuries in China and Japan.

By vulnerability

• resilience

Other

Other	Bony-eared assfish		Fish hold the records for the relative brain weights of vertebrates. Most vertebrate species have similar brain-to-body weight ratios. The deep sea bathypelagic bony-eared assfish^[138] has the smallest ratio of all known vertebrates.^[139]
	Elephantnose fish		At the other extreme, the elephantnose fish, an African freshwater fish, has an exceptionally large brain-to-body weight ratio. These fish have the largest brain-to-body oxygen consumption ratio of all known vertebrates.^[140]
	Hallucinogenic fish		The hallucinogenic dream fish, Sarpa salpa, a species of bream recognizable by the golden stripes running the length of its body, can induce LSD-like hallucinations if it is eaten. These widely distributed coastal fish^[141] became a recreational drug during the Roman Empire, and are called "the fish that make dreams" in Arabic. Other hallucinogenic fish are Siganus spinus,^[142] called "the fish that inebriates" in Reunion Island, and Mulloidichthys samoensis,^[143] called "the chief of ghosts" in Hawaii.^[144]
	Nopoli rockclimbing goby		The Nopoli rockclimbing goby uses its mouth to climb waterfalls by inching up rocks like a caterpillar, using its mouth as a sucker together with another sucker on its stomach. When the fish is young, it undergoes a radical transformation when it moves from saltwater to a freshwater stream. The mouth migrates over a period of two days from the front of its head to its chin. This allows the fish to feed by scraping algae from rocks. Pictured is the goby before and after the transformation.^[145]^[146]
	Vampire fish		Smaller species of vampire fish, native to the Amazon River, have an alleged tendency to burrow into and parasitise the human urethra. However, despite ethnological reports dating back to the late 19th century, the first documented case of the removal of a vampire fish from a human urethra did not occur until 1997, and even that incident has remained a matter of controversy.^[147]

See also

• Diversity of gastropods
• Largest organisms
• List of long-living organisms
• Maximum life span
• Smallest organisms

Notes

1. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Phycodurus eques" in FishBase. July 2009 version.
2. Leafy and Weedy Sea Dragon National Geographic Profile. Retrieved 20 July 2009.
3. Pollom, R. (2017). "Phycodurus eques". IUCN Red List of Threatened Species. 2017: e.T17096A67622420. doi:10.2305/IUCN.UK.2017-2.RLTS.T17096A67622420.en. Retrieved 12 November 2021.
4. Pietsch, T.W. (2005). "New species of the ceratioid anglerfish genus Lasiognathus Regan (Lophiiformes: Thaumatichthyidae) from the Eastern North Atlantic off Madeira" (PDF). Copeia. 2005 (1): 77–81. doi:10.1643/ci-04-184r1. S2CID 84572467.
5. FishBase
6. Estudo das Espécies Ícticas do Parque Estadual do Cantão, fish species survey of Cantão (in Portuguese)
7. Moyle & Cech 2003, p. Chapter 1
8. Nelson, Joseph S. (2006). Fishes of the World. John Wiley & Sons, Inc. p. 2. ISBN 978-0-471-25031-9.
9. Helfman et al. 2009, p. 3
10. Tree of life web project - Chordates.
11. N. A. Campbell and J. B. Reece (2005). Biology Seventh Edition. Benjamin Cummings, San Francisco CA.
12. Clack, J. A. (2002) Gaining Ground. Indiana University
13. Teleost Encyclopædia Britannica Online. 15 July 2009
14. Benton, Michael J. (1990). Vertebrate Paleontology. London: Chapman & Hall. ISBN 978-0-412-54010-3.
15. Ben Waggoner (17 July 1995). "Telostei". Museum of Paleontology, University of California, Berkeley. Retrieved 8 June 2006.
16. Cohen, DM (1970). "How many recent fishes are there?". Proceedings of the California Academy of Sciences. 38 (17): 341–346.
17. Bone & Moore 2008, p. 3
18. CIA Factbook: World.
19. Elert, Glenn Volume of Earth's Oceans. The Physics Factbook. Retrieved 19 April 2008.
20. Wilson RW, Millero FJ, Taylor JR, Walsh PJ, Christensen V, Jennings S and Grosell M (2009) "Contribution of Fish to the Marine Inorganic Carbon Cycle" Science, 323 (5912) 359-362. (This article contains the first ever estimate of global fish biomass)
21. Shiklomanov, I A, (1993) World fresh water resources in Glick, P H, ed., Water in Crisis: Oxford University Press, p 13-24.
22. Horn, MH (1972). "The amount of space available for marine and freshwater fishes" (PDF). NOAA: Fishery Bulletin. 70: 1295–1297.
23. Bone & Moore 2008, p. 35
24. C.Michael Hogan. 2011. Ross Sea. Eds. P.Saundry & C.J.Cleveland. Encyclopedia of Earth. National Council for Science and the Environment. Washington DC
25. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Abyssobrotula galatheae" in FishBase. July 2009 version.
26. Jamieson, A.J., and Yancey, P. H. (2012). On the Validity of the Trieste Flatfish: Dispelling the Myth. The Biological Bulletin 222(3): 171-175
27. Yanceya, P.H.; Gerringera, E.M.; Drazen, J.C.; Rowden, A.A.; and Jamieson, A. (2014). Marine fish may be biochemically constrained from inhabiting the deepest ocean depths. PNAS 111(12): 4461–4465
28. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Triplophysa stoliczkai" in FishBase. July 2009 version.
29. Froese, Rainer; Pauly, Daniel (eds.) (2014). "Astyanax mexicanus" in FishBase. 2014 version.
30. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Thermichthys hollisi" in FishBase. July 2009 version.
31. Antennariidae: Frogfishes Tree of Life Web Project
32. Biological profiles: Sargassumfish Florida Museum of Natural History. Retrieved 2012-01-04.
33. Depczynski, M; Bellwood, DR (2005). "Shortest recorded vertebrate lifespan found in a coral reef fish". Current Biology. 15 (8): R288–R289. doi:10.1016/j.cub.2005.04.016. PMID 15854891. S2CID 22684907.
34. Herrera, M; Jagadeeswaran, P (2004). "Annual Fish as a Genetic Model for Aging". The Journals of Gerontology Series A: Biological Sciences and Medical Sciences. 59 (2): B101–B107. doi:10.1093/gerona/59.2.b101. PMID 14999022.
35. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Cynolebias nigripinnis" in FishBase. July 2009 version.
36. Munk, K. (2001) "Maximum Ages of Groundfishes in Waters off Alaska and British Columbia and Considerations of Age Determination". Alaska Fishery Research Bulletin 8 :1.
37. Cailliet, G.M., Andrews, A.H., Burton, E.J., Watters, D.L., Kline, D.E., Ferry-Graham, L.A. (2001) "Age determination and validation studies of marine fishes: do deep-dwellers live longer?" Exp. Gerontol. 36 : 739–764.
38. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Sebastes aleutianus" in FishBase. July 2009 version.
39. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Hoplostethus atlanticus" in FishBase. July 2009 version.
40. How to Tell Time by a Cat's Eye
41. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Cyprinus carpio" in FishBase. July 2009 version.
42. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Carassius auratus" in FishBase. July 2009 version.
43. Night Tarpon Fishing Trips
44. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Megalops atlanticus" in FishBase. July 2009 version.
45. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Megalops cyprinoides" in FishBase. July 2009 version.
46. Protective Regulations Proposed for Ancient, Imperiled Southern Green Sturgeon 2011-09-28 at the Wayback Machine
47. Contemporaries of the Dinosaurs, Sturgeon Fossils Date Back 200 Million Years April 17, 2009, at the Wayback Machine
48. Sturgeons June 4, 2009, at the Wayback Machine
49. The Oldest Living Fish
50. The Shedd Honors Its Oldest Residen
51. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Neoceratodus forsteri" in FishBase. July 2009 version.
52. Nielsen, Julius; Hedeholm, Rasmus B.; Heinemeier, Jan; Bushnell, Peter G.; Christiansen, Jørgen S.; Olsen, Jesper; Ramsey, Christopher Bronk; Brill, Richard W.; Simon, Malene; Steffensen, Kirstine F.; Steffensen, John F. (2016). "Eye lens radiocarbon reveals centuries of longevity in the Greenland shark (Somniosus microcephalus)". Science. 353 (6300): 702–4. Bibcode:2016Sci...353..702N. doi:10.1126/science.aaf1703. hdl:2022/26597. PMID 27516602. S2CID 206647043.
    • Enrico de Lazaro (12 August 2016). "Greenland Sharks are Longest-Lived Vertebrates on Earth, Marine Biologists Say". Science News.
53. Kottelat M, Britz R, Tan HH and Witte KE (2005) "Paedocypris, a new genus of Southeast Asian cyprinid fish with a remarkable sexual dimorphism, comprises the world's smallest vertebrate" Proceedings of the Royal Society B 273 :895-899.
54. World's smallest fish 2008-12-01 at the Wayback Machine 2006, Natural History Museum
55. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Paedocypris progenetica" in FishBase. July 2009 version.
56. Rittmeyer, Eric N.; Allison, Allen; Gründler, Michael C.; Thompson, Derrick K.; Austin, Christopher C. (2012). "Ecological guild evolution and the discovery of the world's smallest vertebrate". PLoS ONE. Public Library of Science. 7 (1): e29797. Bibcode:2012PLoSO...729797R. doi:10.1371/journal.pone.0029797. PMC 3256195. PMID 22253785.
57. "Scientists find 'smallest fish'". BBC News. 25 January 2006. Retrieved 23 May 2010.
58. What is the smallest species of fish? February 20, 2009, at the Wayback Machine
59. "Smallest fish compete for honours". BBC News. 31 January 2006. Retrieved 23 May 2010.
60. Bragging Rights: The Smallest Fish Ever | LiveScience July 6, 2008, at the Wayback Machine
61. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Schindleria brevipinguis" in FishBase. July 2009 version.
62. Foot, T (2000) Guinness Book of World Records 2001. Guinness World Records Ltd.
63. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Rhincodon typus" in FishBase. July 2009 version.
64. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Mola mola" in FishBase. July 2009 version.
65. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Regalecus glesne" in FishBase. July 2009 version.
66. Mydans, Seth (25 August 2005). "Hunt for the big fish becomes a race". The New York Times. Retrieved 3 March 2013.
67. Giant Catfish May Be World's Largest Freshwater Fish National Geographic, 28 October 2010.
68. Ryan P "Deep-sea creatures: The bathypelagic zone" Te Ara - the Encyclopedia of New Zealand. Updated 21 September 2007.
69. Froese, Rainer, and Daniel Pauly, eds. (2009). "Batrachoididae" in FishBase. September 2009 version.
70. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Opsanus beta" in FishBase. September 2009 version.
71. Moyle & Cech 2003, p. 4
72. Anglerfish Video
73. Theodore W. Pietsch (1975). "Precocious sexual parasitism in the deep sea ceratioid anglerfish, Cryptopsaras couesi Gill". Nature. 256 (5512): 38–40. Bibcode:1975Natur.256...38P. doi:10.1038/256038a0. S2CID 4226567.
74. Froese, Rainer and Pauly, Daniel, eds. (2006). Species of Sphyrna in FishBase. April 2006 version.
75. Froese, Rainer, and Daniel Pauly, eds. (2006). "Lamniforme" in FishBase. April 2006 version.
76. Froese, Rainer, and Daniel Pauly, eds. (2006). "Scyliorhinidae" in FishBase. April 2006 version.
77. Froese, Rainer, and Daniel Pauly, eds. (2006). "Apogonidae" in FishBase. April 2006 version.
78. Froese, Rainer and Pauly, Daniel, eds. (2006). Species of Hippocampus in FishBase. April 2006 version.
79. Liem KF (1980) "Adaptive Significance of Intra- and Interspecific Differences in the Feeding Repertoires of Cichlid Fishes" August 28, 2008, at the Wayback Machine American Zoologist, 20 (1):295-314.
80. Bone & Moore 2008, p. 92
81. Liem KF (1980) "Acquisition of energy by teleosts: adaptive mechanisms and evolutionary patterns". In Environmental Physiology of Fishes (Ed. M A Ali), pp. 299–334. New York, London: Plenum Press.
82. Lauder, GV (1980). "Evolution of the feeding mechanism in primitive actinopterygian fishes: a functional anatomical analysis of Polypterus, Lepisosteus and Amia". J. Morphol. 163 (3): 283–317. doi:10.1002/jmor.1051630305. PMID 30170473. S2CID 26805223.
83. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Epibulus insidiator" in FishBase. July 2009 version.
84. Bone & Moore 2008, p. 190
85. Norton, SF; Bainerd, EL (1993). "Convergence in the feeding mechanics of ecomorphologically similar species in the Centrarchidae and Cichlidae". Journal of Experimental Biology. 176 (1): 11–29. doi:10.1242/jeb.176.1.11.
86. Bone & Moore 2008, p. 189
87. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Prionace glauca" in FishBase. July 2009 version.
88. Leonard J. V. Compagno (1984). Sharks of the World: An annotated and illustrated catalogue of shark species known to date. Food and Agriculture Organization of the United Nations. pp. 521–524, 555–61, 590.
89. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
90. Douglas, M.M.; Bunn, S.E; Davies, P.M. (2005). "River and wetland food webs in Australia's wet-dry tropics: general principles and implications for management" (PDF). Marine and Freshwater Research. 56 (3): 329–342. doi:10.1071/mf04084. hdl:10072/4430.
91. Lowry, D.; Wintzer, A.P.; Matott, M.P.; Whitenack, L.B.; Huber, D.R.; Dean, M.; Motta, P.J. (2005). "Aerial and aquatic feeding in the silver arawana, Osteoglossum bicirrhosum" (PDF). Environmental Biology of Fishes. 73 (4): 453–462. doi:10.1007/s10641-005-3214-4. S2CID 43389710.
92. ""Plastic flies help spitting archer fish regain aim" Telegraph.co.uk". The Telegraph. 11 July 2002. Retrieved 24 May 2009.
93. Schuster, S.; Wöhl, S.; Griebsch, M.; Klostermeier, I. (2006). "Animal Cognition:, How Archer Fish Learn to Down Rapidly Moving Targets" (PDF). Current Biology. 16 (4): 378–383. doi:10.1016/j.cub.2005.12.037. PMID 16488871. S2CID 1139246.
94. Bone & Moore 2008, p. 197
95. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Osteoglossum bicirrhosum" in FishBase. July 2009 version.
96. Carol Martins; Craig Knickle. "Megamouth Shark- Parasites". Florida Museum of Natural History. Retrieved 9 February 2009.
97. Jaine, FRA; Couturier, LIE; Weeks, SJ; Townsend, KA; Bennett, MB; Fiora, K; Richardson, AJ (2012). "When Giants Turn Up: Sighting Trends, Environmental Influences and Habitat Use of the Manta Ray Manta alfredi at a Coral Reef". PLOS ONE. 7 (10): e46170. Bibcode:2012PLoSO...746170J. doi:10.1371/journal.pone.0046170. PMC 3463571. PMID 23056255.
98. Jacobs, GH (1992). "Ultraviolet Vision in Vertebrates". Am. Zool. 32 (4): 544–554. doi:10.1093/icb/32.4.544.
99. Nelson, Joseph, S. (2006). Fishes of the World. John Wiley & Sons, Inc. ISBN 978-0-471-25031-9.
100. Froese, Rainer; Pauly, Daniel (eds.) (2007). "Anableps anableps" in FishBase. Mar 2007 version.
101. Losey, G. S. Jr (2003). "Crypsis and communication functions of UV-visible coloration in two coral reef damselfish, Dascyllus aruanus and D. reticulatus". Animal Behaviour. 66 (2): 299–307. doi:10.1006/anbe.2003.2214. S2CID 140204848.
102. Siebeck, UE; Parker, AN; Sprenger, D; Mäthger, LM; Wallis, G (2010). "A Species of Reef Fish that Uses Ultraviolet Patterns for Covert Face Recognition" (PDF). Current Biology. 20 (5): 407–410. doi:10.1016/j.cub.2009.12.047. PMID 20188557. S2CID 3743161.
103. Helfman et al., 2009, pp. 84-87.
104. Robison, BH; Reisenbichler, KR (2008). "Macropinna microstoma and the Paradox of Its Tubular Eyes". Copeia. 2008 (4): 780–784. doi:10.1643/CG-07-082. S2CID 85768623.
105. Researchers solve mystery of deep-sea fish with tubular eyes and transparent head Monterey Bay Aquarium Research Institute, 23 February 2009.
106. Froese, Rainer; Pauly, Daniel (eds.) (2011). "Macropinna microstoma" in FishBase. September 2011 version.
107. Morin, James G.; Harrington, Anne; Nealson, Kenneth; Krieger, Neil; Baldwin, Thomas O.; Hastings, J. W. (1975). "Light for All Reasons: Versatility in the Behavioral Repertoire of the Flashlight Fish". Science. 190 (4209): 74–76. Bibcode:1975Sci...190...74M. doi:10.1126/science.190.4209.74. S2CID 83905458.
108. McCosker JE (1977) "Flashlight fishes" 2012-05-02 at the Wayback Machine Scientific American, 236: 106–115.
109. Paxton, John R. (1998). Paxton, J.R.; Eschmeyer, W.N. (eds.). Encyclopedia of Fishes. San Diego: Academic Press. p. 162. ISBN 978-0-12-547665-2.
110. Matsura, Keiichi; Tyler, James C. (1998). Paxton, J.R.; Eschmeyer, W.N. (eds.). Encyclopedia of Fishes. San Diego: Academic Press. pp. 229–230. ISBN 978-0-12-547665-2.
111. Guinness Book of World Records (2009)
112. R. Aidan Martin. "Biology of the Shortfin Mako". ReefQuest Centre for Shark Research. Retrieved 12 August 2006.
113. Passarelli, Nancy; Craig Knickle; Kristy DiVittorio. "SHORTFIN MAKO". Florida Museum of Natural History. Retrieved 6 October 2008.
114. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
115. "BBC article and video of flying fish". bbc.co.uk. 20 May 2008. Retrieved 20 May 2008.
116. . Archived from the original on 8 January 2015. Retrieved 26 February 2015.
117. Poisonous vs. Venomous fish: What's the difference? 2009-10-30 at the Wayback Machine Reef Biosearch. Retrieved 17 July 2009.
118. Smith, WL; Wheeler, WC (2006). "Venom Evolution Widespread in Fishes: A Phylogenetic Road Map for the Bioprospecting of Piscine Venoms". Journal of Heredity. 97 (3): 206–217. doi:10.1093/jhered/esj034. PMID 16740627.
119. Venomous Fish Outnumber Snakes, LiveScience, 22 August 2006.
120. Grady, Denise Venom Runs Thick in Fish Families, Researchers Learn The New York Times 22 August 2006.
121. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Lactophrys bicaudalis" in FishBase. July 2009 version.
122. Lieske, E. and Myers, R.F. (2004) Coral reef guide; Red Sea London, HarperCollins ISBN 0-00-715986-2
123. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Gymnothorax javanicus" in FishBase. July 2009 version.
124. Rongo, T; Bush, M; van Woesik, R (2009). "Did ciguatera prompt the late Holocene Polynesian voyages of discovery?". Journal of Biogeography. 36 (8): 1423–1432. doi:10.1111/j.1365-2699.2009.02139.x.
125. Voyages of discovery or necessity? Fish poisoning may be why Polynesians left paradise PhysOrg.com, 18 May 2009.
126. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Synanceja verrucosa" in FishBase. July 2009 version.
127. "The Stonefish – The Deadliest Fish in The World", Virginia Wells, Petplace.com.
128. Reef Stonefish, Synanceia verrucosa (Bloch & Schneider, 1801) Australian Museum. Retrieved 21 July 2009.
129. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Pterois volitans" in FishBase. July 2009 version.
130. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Uranoscopus sulphureus" in FishBase. July 2009 version.
131. Taylor, Geoff (March 2000). (PDF). Journal of the South Pacific Underwater Medicine Society. 30 (1): 7–8. ISSN 0813-1988. OCLC 16986801. Archived from the original on 10 June 2015. Retrieved 10 June 2015.{{cite journal}}: CS1 maint: unfit URL (link)
132. Bone & Moore 2008, p. 442
133. Bone & Moore 2008, p. 443
134. Armstrong, MJ; Gerritsenb, HD; Allenc, M; McCurdya, WJ; Peel, JAD (2004). "Variability in maturity and growth in a heavily exploited stock: cod (Gadus morhua L.) in the Irish Sea". Journal of Marine Science. 61 (1): 98–112. doi:10.1016/j.icesjms.2003.10.005.
135. Angling Retains its Mainstream Appeal and Broad Economic Impact-American Sportfishing Association 2008-05-13 at the Wayback Machine
136. NOAA Fisheries: Recreational Fishing Services.
137. Clover, Charles (2004). The End of the Line: How Overfishing Is Changing the World and What We Eat. Ebury Press. ISBN 978-0-09-189780-2.
138. Froese, Rainer; Pauly, Daniel (eds.) (2014). "Acanthonus armatus" in FishBase. January 2014 version.
139. Fine, ML; Horn, MH; Cox, B (1987). "Acanthonus armatus, a Deep-Sea Teleost Fish with a Minute Brain and Large Ears". Proceedings of the Royal Society B. 230 (1259): 257–265. Bibcode:1987RSPSB.230..257F. doi:10.1098/rspb.1987.0018. PMID 2884671. S2CID 19183523.
140. Nilsson G (1996) "Brain and body oxygen requirements of Gnathonemus petersii, a fish with an exceptionally large brain" Journal of Experimental Biology, 199(3): 603-607. Download
141. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Sarpa salpa" in FishBase. October 2009 version.
142. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Siganus spinus" in FishBase. October 2009 version.
143. Froese, Rainer; Pauly, Daniel (eds.) (2009). "Mulloidichthys samoensis" in FishBase. October 2009 version.
144. de Haro, Luc and Pommier, Philip (2006) Hallucinatory Fish Poisoning (Ichthyoallyeinotoxism): Two Case Reports From the Western Mediterranean and Literature Review Clinical Toxicology, 44:185–188. Download
145. Cullen, JA; Maie, T; Schoenfuss, HL; Blob, RW (2012). "Evolutionary novelty versus exaptation: Oral kinematics in feeding versus climbing in the waterfall-climbing Hawaiian goby Sicyopterus stimpsoni". PLOS ONE. 8 (1): e53274. Bibcode:2013PLoSO...853274C. doi:10.1371/journal.pone.0053274. PMC 3537660. PMID 23308184.
146. Meet the amazing, waterfall-climbing fish 2013-02-24 at the Wayback Machine Science, 13 January 2013.
147. Ricciuti, Edward R.; Bird, Jonathan (2003). Killers of the Seas: The Dangerous Creatures That Threaten Man in an Alien Environment. The Lyons Press. ISBN 978-1-58574-869-3.

References

• Bone, Q; Moore, R H (2008). Biology of Fishes. Taylor & Francis Group. ISBN 978-0-415-37562-7. [1] at Google Books
• Moyle, PB; Cech, J. J. (2003). Fishes, An Introduction to Ichthyology (5th ed.). Benjamin Cummings. ISBN 978-0-13-100847-2.
• Helfman, G.; Collette; Facey, D.; Bowen, BW (2009). The Diversity of Fishes: Biology, Evolution, and Ecology. Wiley-Blackwell. p. 3. ISBN 978-1-4051-2494-2.
• Weis, Judith S (2011) Do Fish Sleep?: Fascinating Answers to Questions about Fishes Rutgers University Press. ISBN 9780813549415.

External links

• Articles About Marine Life Oceans for Youth Foundation.
• The 20 weirdest fish in the ocean Christian Science Monitor. 22 February 22, 2010.