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→‎Shoaling and schooling: adapt materials from Teleost, see there for attrib.
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[[File:School of Pterocaesio chrysozona in Papua New Guinea 1.jpg|thumb|These [[goldband fusilier]]s are [[Shoaling and schooling|schooling]] because their swimming is synchronised.|alt=Photo of thousands of fish separated from each other by distances of {{convert|2|in}} or less]]
[[File:School of Pterocaesio chrysozona in Papua New Guinea 1.jpg|thumb|These [[goldband fusilier]]s are [[Shoaling and schooling|schooling]] because their swimming is synchronised.|alt=Photo of thousands of fish separated from each other by distances of {{convert|2|in}} or less]]


An assemblage of fish merely using some localised resource such as food or nesting sites is called an ''aggregation''. A ''shoal'' is a loosely organised group where each fish swims and forages independently but is attracted to other members of the group and adjusts its behaviour, such as swimming speed, so that it remains close to the other members of the group. A ''school'' is a much more tightly organised group, synchronising its swimming so that all fish move at the same speed and in the same direction. Shoaling and schooling provide a variety of advantages.{{sfn|Helfman|Collette|Facey|1997|p=375}}
An assemblage of fish merely using some localised resource such as food or nesting sites is called an ''aggregation''. A ''shoal'' is a loosely organised group where each fish swims and forages independently but is attracted to other members of the group and adjusts its behaviour, such as swimming speed, so that it remains close to the other members of the group. A ''school'' is a much more tightly organised group, synchronising its swimming so that all fish move at the same speed and in the same direction.{{sfn|Helfman|Collette|Facey|1997|p=375}}
Schooling is sometimes an [[antipredator adaptation]], offering improved vigilance against predators. It is often more efficient to gather food by working as a group, and individual fish optimise their strategies by choosing to join or leave a shoal. When a predator has been noticed, prey fish respond defensively, resulting in collective shoal behaviours such as synchronised movements. Responses do not consist only of attempting to hide or flee; antipredator tactics include for example scattering and reassembling. Fish also aggregate in shoals to spawn.<ref>{{cite book |last=Pitcher |first=Tony J. |chapter=12. Functions of Shoaling Behaviour in Teleosts |title=The Behaviour of Teleost Fishes |publisher=Springer |year=1986 |pages=294–337 |doi=10.1007/978-1-4684-8261-4_12 |isbn=978-1-4684-8263-8}}</ref>


=== Communication ===
=== Communication ===

Revision as of 14:01, 4 February 2024

Fish
Temporal range: 535–0 Ma Middle CambrianRecent
Diversity of various fish including sharks, stingrays, bony fish, jawless fish, and coelacanths.
Diversity of various fish including sharks, stingrays, bony fish, jawless fish, and coelacanths.
Scientific classificationEdit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Olfactores
Subphylum: Vertebrata
Groups included
Jawless fish
Armoured fish
Spiny sharks
Cartilaginous fish
Bony fish
Ray-finned fish
Lobe-finned fish
Cladistically included but traditionally excluded taxa
Tetrapods

A fish (pl.: fish or fishes) is an aquatic, gill-bearing animal with a hard skull that lacks limbs with digits. This includes hagfish, lampreys, and both cartilaginous and bony fish. Approximately 95% of living fish species are ray-finned bony fish; around 99% of those are teleosts. As a group, if tetrapods are excluded, fish are paraphyletic and so do not form a taxonomic group.[1][2]

The earliest organisms that can be classified as fish were soft-bodied chordates that first appeared during the Cambrian period. Although they lacked a true spine, they possessed notochords which allowed them to be more agile than their invertebrate counterparts. Fish would continue to evolve through the Paleozoic era, diversifying into a wide variety of forms. Many fish of the Paleozoic developed external armor that protected them from predators. The first fish with jaws appeared in the Silurian period, after which many (such as sharks) became formidable marine predators rather than just the prey of arthropods.

Most fish are ectothermic ("cold-blooded"), allowing their body temperatures to vary as ambient temperatures change, though some of the large active swimmers like white shark and tuna can hold a higher core temperature.[3][4] Fish can acoustically communicate with each other, most often in the context of feeding, aggression or courtship.[5]

Fish are abundant in most bodies of water. They can be found in nearly all aquatic environments, from high mountain streams (e.g., char and gudgeon) to the abyssal and even hadal depths of the deepest oceans (e.g., cusk-eels and snailfish), although no species has yet been documented in the deepest 25% of the ocean.[6] With 34,300 described species, fish exhibit greater species diversity than any other group of vertebrates.[7]

Fish are an important resource for humans worldwide, especially as food. Commercial and subsistence fishers hunt fish in wild fisheries or farm them in ponds or in cages in the ocean (in aquaculture). They are also caught by recreational fishers, kept as pets, raised by fishkeepers, and exhibited in public aquaria. Fish have had a role in culture through the ages, serving as deities, religious symbols, and as the subjects of art, books and movies.

Etymology

The word fish is inherited from Proto-Germanic, and is related to the Latin piscis and Old Irish īasc, though the exact root is unknown; some authorities reconstruct a Proto-Indo-European root *peysk-, attested only in Italic, Celtic, and Germanic.[8][9][10][11]

Evolution

Fish, as vertebrata, developed as sister of the tunicata. As the tetrapods emerged deep within the fishes group, as sister of the lungfish, characteristics of fish are typically shared by tetrapods, including having vertebrae and a cranium.

Drawing of animal with large mouth, long tail, very small dorsal fins, and pectoral fins that attach towards the bottom of the body, resembling lizard legs in scale and development.[12]
Dunkleosteus was a gigantic prehistoric fish of class Placodermi.

Early fish from the fossil record are represented by a group of small, jawless, armored fish known as ostracoderms. Jawless fish lineages are mostly extinct. An extant clade, the lampreys may approximate ancient pre-jawed fish. The first jaws are found in Placodermi fossils. They lacked distinct teeth, having instead the oral surfaces of their jaw plates modified to serve the various purposes of teeth. The diversity of jawed vertebrates may indicate the evolutionary advantage of a jawed mouth. It is unclear if the advantage of a hinged jaw is greater biting force, improved respiration, or a combination of factors.

Fish may have evolved from a creature similar to a coral-like sea squirt, whose larvae resemble primitive fish in important ways. The first ancestors of fish may have kept the larval form into adulthood (as some sea squirts do today).

Phylogeny

Fishes are a paraphyletic group: that is, any clade containing all fish also contains the tetrapods. The latter are not fish, though they include fish-shaped forms, such as Whales and Dolphins (see evolution of cetaceans) or the extinct ichthyosaurs, both of which convergently acquired a fish-like body shape due to secondary aquatic adaptation. In a cladistic sense, tetrapods are a subset of Osteichthyes.

...it is increasingly widely accepted that tetrapods, including ourselves, are simply modified bony fishes, and so we are comfortable with using the taxon Osteichthyes as a clade, which now includes all tetrapods...

Fishes of the World[13]

The following cladogram shows clades – some with, some without extant relatives – that are traditionally considered as "fishes" (cyan line) and the tetrapods (four-limbed vertebrates), which are mostly terrestrial. Extinct groups are marked with a dagger (†).

Vertebrata/

Euconodonta

Pteraspidomorphi

Thelodonti

Anaspida

Galeaspida

Pituriaspida

Osteostraci

Gnathostomata

"†Placodermi" (armoured fishes, paraphyletic)[14]

"†Acanthodii" ("spiny sharks", paraphyletic or polyphyletic)[15]

Chondrichthyes
(cartilaginous fishes)
Euteleostomi/

"†Acanthodii" ("spiny sharks", paraphyletic or polyphyletic)

Actinopterygii
(ray‑finned fishes)
Sarcopterygii
(lobe‑finned fish)
Osteichthyes
(jawed vertebrates)
"Fishes"
Craniata

Taxonomy

Leedsichthys is the largest known fish, with a maximum length of 16 metres (52 ft).

Fishes are a paraphyletic group and for this reason, groups such as the class Pisces seen in older reference works are no longer used in formal classifications. Traditional classification divides fish into three extant classes, and with extinct forms sometimes classified within the tree, sometimes as their own classes:[16]

The above scheme is the one most commonly encountered in non-specialist and general works. Many of the above groups are paraphyletic, in that they have given rise to successive groups: Agnatha are ancestral to Placodermi, who again have given rise to Osteichthyes, as well as to Acanthodii, the ancestors of Chondrichthyes. With the arrival of phylogenetic nomenclature, the fishes has been split up into a more detailed scheme, with the following major groups:

† – indicates extinct taxon
Some palaeontologists contend that because Conodonta are chordates, they are primitive fish. For a fuller treatment of this taxonomy, see the vertebrate article.

The position of hagfish in the phylum Chordata is not settled. Phylogenetic research in 1998 and 1999 supported the idea that the hagfish and the lampreys form a natural group, the Cyclostomata, that is a sister group of the Gnathostomata.[17][18]

Fish account for more than half of vertebrate species. As of 2016, there are over 32,000 described species of bony fish, over 1,100 species of cartilaginous fish, and over 100 hagfish and lampreys. A third of these fall within the nine largest families; from largest to smallest, these are Cyprinidae, Gobiidae, Cichlidae, Characidae, Loricariidae, Balitoridae, Serranidae, Labridae, and Scorpaenidae. About 64 families are monotypic, containing only one species.[13]

Diversity

Photo of fish with many narrow, straight appendages. Some are end in points, and others are longer, ending in two or three approximately flat, triangular flaps, each with a dark spot.
A relative of the seahorses, the leafy seadragon's appendages allow it to camouflage (in the form of crypsis) with the surrounding seaweed.
The psychedelic mandarin dragonet is one of only two fish species where the blue colouring has been shown to be due to blue pigment-containing chromatophores in the skin.[19]

The term "fish" most precisely describes any non-tetrapod craniate (i.e. an animal with a skull and in most cases a backbone) that has gills throughout life and whose limbs, if any, are in the shape of fins.[20] Unlike groupings such as birds or mammals, fish are not a single clade but a paraphyletic collection of taxa, including hagfishes, lampreys, sharks and rays, ray-finned fish, coelacanths, and lungfish.[21][22] Indeed, lungfish and coelacanths are closer relatives of tetrapods (such as mammals, birds, amphibians, etc.) than of other fish such as ray-finned fish or sharks, so the last common ancestor of all fish is also an ancestor to tetrapods. As paraphyletic groups are no longer recognised in modern systematic biology, the use of the term "fish" as a biological group must be avoided.

A typical fish is ectothermic, has a streamlined body for rapid swimming, extracts oxygen from water using gills or uses an accessory breathing organ to breathe atmospheric oxygen, has two sets of paired fins, usually one or two (rarely three) dorsal fins, an anal fin, and a tail fin, has jaws, has skin that is usually covered with scales, and lays eggs. Each criterion has exceptions. Tuna, swordfish, and some species of sharks show some warm-blooded adaptations – they can heat their bodies significantly above ambient water temperature.[21] Streamlining and swimming performance varies from fish such as tuna, salmon, and jacks that can cover 10–20 body-lengths per second to species such as eels and rays that swim no more than 0.5 body-lengths per second.[23] Many groups of freshwater fish extract oxygen from the air as well as from the water using a variety of different structures. Lungfish have paired lungs similar to those of tetrapods, gouramis have a structure called the labyrinth organ that performs a similar function, while many catfish, such as Corydoras extract oxygen via the intestine or stomach.[24] Body shape and the arrangement of the fins is highly variable, covering such seemingly un-fishlike forms as seahorses, pufferfish, anglerfish, and gulpers. Similarly, the surface of the skin may be naked (as in moray eels), or covered with scales of a variety of different types usually defined as placoid (typical of sharks and rays), cosmoid (fossil lungfish and coelacanths), ganoid (various fossil fish but also living gars and bichirs), cycloid, and ctenoid (these last two are found on most bony fish).[25] Fish range in size from the huge 16-metre (52 ft) whale shark to the tiny 8-millimetre (0.3 in) stout infantfish.

The diversity of living fish is unevenly distributed among the various groups, with teleosts making up the bulk of living fishes (96%).[26] The following cladogram[27] shows the evolutionary relationships of all groups of living fishes (with their respective diversity[26][28]) and the four-limbed vertebrates (tetrapods).

Vertebrates

Jawless fish (118 living species: hagfish, lampreys)

Jawed vertebrates

Cartilaginous fishes (>1,100 living species: sharks, rays, chimaeras)

Bony fishes
Lobe-finned fish
Rhipidistia

Tetrapoda (>30,000 living species: amphibians, mammals, reptiles, birds)

Dipnoi (6 living species: lungfish)

Actinistia (2 living species: coelacanths)

Ray-finned fish

Cladistia (14 living species: bichirs, reedfish)

Actinopteri

Chondrostei (27 living species: sturgeons, paddlefish)

Neopterygii
Holostei

Ginglymodi (7 living species: gars, alligator gars)

Halecomorphi (2 living species: bowfin, eyetail bowfin)

Teleostei (>32,000 living species)

Ecology

Fish species are roughly divided equally between marine (oceanic) and freshwater ecosystems. Coral reefs in the Indo-Pacific constitute the center 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.[29]

The deepest living fish in the ocean so far found is the snailfish (Pseudoliparis belyaevi) which was filmed in the Izu-Ogasawara Trench off the coast of Japan at 8,336 meters in August 2022. The fish was filmed by a robotic lander as part of a scientific expedition funded by Victor Vescovo's Caladan Oceanic with the scientific team led by Professor Alan Jamieson of the University of Western Australia.[30]

A few fish live mostly on land or lay their eggs on land near water.[31] Mudskippers feed and interact with one another on mudflats and go underwater to hide in their burrows.[32] A single undescribed species of Phreatobius has been called a true "land fish" as this worm-like catfish strictly lives among waterlogged leaf litter.[33][34] Cavefish of multiple species live in underground lakes, underground rivers or aquifers.[35]

Anatomy and physiology

Respiration

Gills

Tuna gills inside the head, seen from the rear. Water flows through the mouth and over the gills, either pumped or as the fish swims. Blood is circulated through the gills, picking up oxygen and releasing carbon dioxide.

Most fish exchange gases using gills on either side of the pharynx. Gills consist of threadlike structures called filaments. Each filament contains a capillary network that provides a large surface area for exchanging oxygen and carbon dioxide. Fish exchange gases by pulling oxygen-rich water through their mouths and pumping it over their gills. In some fish, capillary blood flows in the opposite direction to the water, causing countercurrent exchange. The gills push the oxygen-poor water out through openings in the sides of the pharynx. Some fish, like sharks and lampreys, possess multiple gill openings. However, bony fish have a single gill opening on each side. This opening is hidden beneath a protective bony cover called an operculum. Juvenile bichirs have external gills, a primitive feature shared with larval amphibians.

Air breathing

Fish from multiple groups can live out of the water for extended periods. Amphibious fish such as the mudskipper can move about on land and live in oxygen-depleted water. The skin of anguillid eels may absorb oxygen directly. The buccal cavity of the electric eel may breathe air. Catfish of the families Loricariidae, Callichthyidae, and Scoloplacidae absorb air through their digestive tracts.[36] Lungfish, with the exception of the Australian lungfish, and bichirs have paired lungs similar to those of tetrapods and must surface to gulp fresh air through the mouth and pass spent air out through the gills. Gar and bowfin have a vascularized swim bladder that functions in the same way. Loaches, trahiras, and many catfish breathe by passing air through the gut. Mudskippers breathe by absorbing oxygen across the skin (similar to frogs). Some fish have evolved accessory breathing organs: labyrinth fish such as gouramis and bettas have a labyrinth organ above the gills, while snakeheads, pikeheads, and Clariidae catfish have similar structures.

Some air-breathing fish are able to survive in damp burrows for weeks without water, entering a state of aestivation (summertime hibernation) until water returns.

Air breathing fish can be divided into obligate air breathers and facultative air breathers. Obligate air breathers, such as the African lungfish, must breathe air periodically or they suffocate. Facultative air breathers, such as the catfish Hypostomus plecostomus, only breathe air if they need to and will otherwise rely on their gills for oxygen. Most air breathing fish are facultative air breathers that avoid the energetic cost of rising to the surface and the fitness cost of exposure to surface predators.[36]

Circulation

Didactic model of a fish heart

Fish have a closed-loop circulatory system. The heart pumps the blood in a single loop throughout the body, with two chambers; for comparison, the mammal heart has two loops through the body and four chambers.[37] The first part is the sinus venosus, a thin-walled sac that collects blood from the fish's veins before allowing it to flow to the second part, the atrium, which is a large muscular chamber. The atrium serves as a one-way antechamber, sends blood to the third part, ventricle. The ventricle is another thick-walled, muscular chamber and it pumps the blood, first to the fourth part, bulbus arteriosus, a large tube, and then out of the heart. The bulbus arteriosus connects to the aorta, through which blood flows to the gills for oxygenation.

Digestion

Jaws allow fish to eat a wide variety of food, including plants and other organisms. Fish ingest food through the mouth and break it down in the esophagus. In the stomach, food is further digested and, in many fish, processed in finger-shaped pouches called pyloric caeca, which secrete digestive enzymes and absorb nutrients. Organs such as the liver and pancreas add enzymes and various chemicals as the food moves through the digestive tract. The intestine completes the process of digestion and nutrient absorption.

Excretion

Most fish release their nitrogenous wastes as ammonia. This may be excreted through the gills or filtered by the kidneys.

Saltwater fish tend to lose water by osmosis; their kidneys return water to the body, and produce a concentrated urine. The reverse happens in freshwater fish: they tend to gain water osmotically, and produce a dilute urine. Some fish have kidneys able to operate in both freshwater to saltwater.

Brain

Diagram showing the pairs of olfactory, telencephalon, and optic lobes, followed by the cerebellum and the mylencephalon
Diagram of rainbow trout brain, from above

Fish have small brains relative to body size compared with other vertebrates, typically one-fifteenth the brain mass of a similarly-sized bird or mammal.[38] However, some fish have relatively large brains, notably mormyrids and sharks, which have brains about as large for their body weight as birds and marsupials.[39] Fish brains are divided into several regions. At the front are the olfactory lobes, a pair of structures that receive and process signals from the nostrils via the two olfactory nerves.[38] The olfactory lobes are very large in fish that hunt primarily by smell, such as hagfish, sharks, and catfish. Behind the olfactory lobes is the two-lobed telencephalon, the structural equivalent to the cerebrum in higher vertebrates. In fish the telencephalon is concerned mostly with olfaction. Together these structures form the forebrain.[38] Connecting the forebrain to the midbrain is the diencephalon (in the diagram, this structure is below the optic lobes and consequently not visible). The diencephalon performs functions associated with hormones and homeostasis.[38] The pineal body lies just above the diencephalon. This structure detects light, maintains circadian rhythms, and controls color changes.[38] The midbrain (or mesencephalon) contains the two optic lobes. These are very large in species that hunt by sight, such as rainbow trout and cichlids.[38] The hindbrain (or metencephalon) is particularly involved in swimming and balance.[38] The cerebellum is a single-lobed structure that is typically the biggest part of the brain.[38] Hagfish and lampreys have relatively small cerebellae, while the mormyrid cerebellum is massive and apparently involved in their electrical sense.[38] The brain stem or myelencephalon is the brain's posterior.[38] As well as controlling some muscles and body organs, in bony fish at least, the brain stem governs respiration and osmoregulation.[38]

Sensory systems

The lateral line system is a network of sensors in the skin which detects gentle currents and vibrations, and senses the motion of nearby fish, whether predators or prey.[40] This can be considered both a sense of touch and of hearing. Blind cave fish navigate almost entirely through the sensations from their lateral line system.[41] Some fish, such as catfish and sharks, have the ampullae of Lorenzini, electroreceptors that detect weak electric currents on the order of millivolt.[42] Vision in fishes is an important sensory system. Fish eyes are similar to those of terrestrial vertebrates like birds and mammals, but have a more spherical lens. Their retinas generally have both rods and cones (for scotopic and photopic vision); most species have colour vision. Some fish can see ultraviolet, while others can see polarized light. Amongst jawless fish, the lamprey has well-developed eyes, while the hagfish has only primitive eyespots.[43] Hearing too is an important sensory system in fish. Fish sense sound using their lateral lines and otoliths in their ears, inside their heads. Some can detect sound through the swim bladder.[44] Some fish, including salmon, are capable of magnetoreception; when the axis of a magnetic field is changed around a circular tank of young fish, they reorient themselves in line with the field.[45][46] The mechanism of fish magnetoreception remains unknown;[47] experiments in birds imply a quantum radical pair mechanism.[48]

Cognition

The cognitive capacities of fish include self-awareness, as seen in mirror tests. Manta rays and wrasses placed in front of a mirror repeatedly check whether their reflection's behavior mimics their body movement.[49][50][51] Choerodon wrasse, archerfish, and Atlantic cod can solve problems and invent tools.[52] The monogamous cichlid Amatitlania siquia exhibits pessimistic behavior when prevented from being with its partner.[53] Fish orient themselves using landmarks; they may use mental maps based on multiple landmarks. Fish behavior in mazes reveals that they possess spatial memory and visual discrimination.[54] Fish have pain and fear responses; toadfish grunt when electrically shocked and over time come to grunt at the mere sight of an electrode.[55] Rainbow trout rock their bodies and rub their lips when injected with bee venom and acetic acid, apparently attempting to relieve pain.[56][57] The wrasse's neurons fired in a pattern resembling human neuronal patterns.[57] The claims have been called flawed as they do not prove that fish possess conscious awareness, especially not human-like awareness,[58] and their brains are very different.[59]

Locomotion

The anatomy of Lampanyctodes hectoris (1) operculum (gill cover), (2) lateral line, (3) dorsal fin, (4) fat fin, (5) caudal peduncle, (6) caudal fin, (7) anal fin, (8) photophores, (9) pelvic fins (paired), (10) pectoral fins (paired)
Photo of white bladder that consists of a rectangular section and a banana-shaped section connected by a much thinner element
Swim bladder of a rudd (Scardinius erythrophthalmus)

Most fish move by alternately contracting paired sets of muscles on either side of the backbone. These contractions form S-shaped curves that move down the body. As each curve reaches the back fin, backward force is applied to the water, and in conjunction with the fins, moves the fish forward. The fish's fins function like an airplane's flaps. Fins also increase the tail's surface area, increasing speed.[60]

The streamlined body of the fish decreases the amount of friction from the water. Since body tissue is denser than water, fish must compensate for the difference or they will sink. Many bony fish have an internal organ called a swim bladder that adjusts their buoyancy through manipulation of gases. The scales of fish originate from the mesoderm (skin); they may be similar in structure to teeth.

Endothermy

Although most fish are exclusively ectothermic, there are exceptions. The only known bony fishes (infraclass Teleostei) that exhibit endothermy are in the suborder Scombroidei – which includes the billfishes, tunas, and the butterfly kingfish, a basal species of mackerel[61] – and also the opah. The opah, a lampriform, was demonstrated in 2015 to use "whole-body endothermy", generating heat with its swimming muscles to warm its body while countercurrent exchange (as in respiration) minimizes heat loss.[62] It is able to actively hunt prey such as squid and swim for long distances due to the ability to warm its entire body, including its heart,[63] which is a trait typically found only in mammals and birds (in the form of homeothermy). In the cartilaginous fishes (class Chondrichthyes), sharks of the families Lamnidae (porbeagle, mackerel, salmon, and great white sharks) and Alopiidae (thresher sharks) exhibit endothermy. The degree of endothermy varies from the billfishes, which warm only their eyes and brain, to the bluefin tuna and the porbeagle shark, which maintain body temperatures in excess of 20 °C (68 °F) above ambient water temperatures.[61]

Endothermy, though metabolically costly, is thought to provide advantages such as increased muscle strength, higher rates of central nervous system processing, and higher rates of digestion.

Reproduction

Ovary of fish (Corumbatá)

The primary reproductive organs are testicles and ovaries. In most species, gonads are paired organs of similar size, which can be partially or totally fused.[64] Some fish have secondary organs that increase reproductive fitness.

In terms of spermatogonia distribution, the structure of teleosts testes has two types: in the most common, spermatogonia occur all along the seminiferous tubules, while in atherinomorph fish they are confined to the distal portion of these structures. Fish can present cystic or semi-cystic spermatogenesis in relation to the release phase of germ cells in cysts to the seminiferous tubules lumen.[64]

Fish ovaries may be of three types: gymnovarian, secondary gymnovarian or cystovarian. In the first type, the oocytes are released directly into the coelomic cavity and then enter the ostium, then through the oviduct and are eliminated. Secondary gymnovarian ovaries shed ova into the coelom from which they go directly into the oviduct. In the third type, the oocytes are conveyed to the exterior through the oviduct.[65] Gymnovaries are the primitive condition found in lungfish, sturgeon, and bowfin. Cystovaries characterize most teleosts, where the ovary lumen has continuity with the oviduct.[64] Secondary gymnovaries are found in salmonids and a few other teleosts.

Oogonia development in teleosts fish varies according to the group, and the determination of oogenesis dynamics allows the understanding of maturation and fertilization processes. Changes in the nucleus, ooplasm, and the surrounding layers characterize the oocyte maturation process.[64] Postovulatory follicles are structures formed after oocyte release; they do not have endocrine function, present a wide irregular lumen, and are rapidly reabsorbed in a process involving the apoptosis of follicular cells. A degenerative process called follicular atresia reabsorbs vitellogenic oocytes not spawned. This process can also occur, but less frequently, in oocytes in other development stages.[64]

Some fish, like the California sheephead, are hermaphrodites, having both testes and ovaries either at different phases in their life cycle or, as in hamlets, have them simultaneously.

Over 97% of fish are oviparous,[66] that is, the eggs develop outside the mother's body. Examples of oviparous fish include salmon, goldfish, cichlids, tuna, and eels. In the majority of these species, fertilisation takes place outside the mother's body, with the male and female fish shedding their gametes into the surrounding water. However, a few oviparous fish practice internal fertilization, with the male using some sort of intromittent organ to deliver sperm into the genital opening of the female, most notably the oviparous sharks, such as the horn shark, and oviparous rays, such as skates. In these cases, the male is equipped with a pair of modified pelvic fins known as claspers.

Marine fish can produce high numbers of eggs which are often released into the open water column. The eggs have an average diameter of 1 millimetre (0.04 in).

The newly hatched young of oviparous fish are called larvae. They are usually poorly formed, carry a large yolk sac (for nourishment), and do not resemble juvenile or adult fish. The larval period in oviparous fish is usually only someweeks, and larvae rapidly grow and change in structure to become juveniles. During this transition, larvae must switch from their yolk sac to feeding on zooplankton prey, a process which depends on typically inadequate zooplankton density, starving many larvae.

In ovoviviparous fish the eggs develop inside the mother's body after internal fertilization but receive little or no nourishment directly from the mother, depending instead on the yolk. Each embryo develops in its own egg. Familiar examples of ovoviviparous fish include guppies, angel sharks, and coelacanths.

Some species of fish are viviparous. In such species the mother retains the eggs and nourishes the embryos. Typically, viviparous fish have a structure analogous to the placenta seen in mammals connecting the mother's blood supply with that of the embryo. Examples of viviparous fish include the surf-perches, splitfins, and lemon shark. Some viviparous fish exhibit oophagy, in which the developing embryos eat other eggs produced by the mother. This has been observed primarily among sharks, such as the shortfin mako and porbeagle, but is known for a few bony fish as well, such as the halfbeak Nomorhamphus ebrardtii.[67] Intrauterine cannibalism is an even more unusual mode of vivipary, in which the largest embryos eat weaker and smaller siblings. This behavior is also most commonly found among sharks, such as the grey nurse shark, but has also been reported for Nomorhamphus ebrardtii.[67]

Behavior

Shoaling and schooling

Photo of thousands of fish separated from each other by distances of 2 inches (51 mm) or less
These goldband fusiliers are schooling because their swimming is synchronised.

An assemblage of fish merely using some localised resource such as food or nesting sites is called an aggregation. A shoal is a loosely organised group where each fish swims and forages independently but is attracted to other members of the group and adjusts its behaviour, such as swimming speed, so that it remains close to the other members of the group. A school is a much more tightly organised group, synchronising its swimming so that all fish move at the same speed and in the same direction.[68] Schooling is sometimes an antipredator adaptation, offering improved vigilance against predators. It is often more efficient to gather food by working as a group, and individual fish optimise their strategies by choosing to join or leave a shoal. When a predator has been noticed, prey fish respond defensively, resulting in collective shoal behaviours such as synchronised movements. Responses do not consist only of attempting to hide or flee; antipredator tactics include for example scattering and reassembling. Fish also aggregate in shoals to spawn.[69]

Communication

Fish communicate by transmitting sounds, acoustic signals, to each other. This is most often in the context of feeding, aggression or courtship.[5] The sounds emitted vary with the species and stimulus involved. Fish can produce either stridulatory sounds by moving components of the skeletal system, or can produce non-stridulatory sounds by manipulating specialized organs such as the swimbladder.[70]

French grunt fish makes sounds by grinding its teeth.

Some fish produce sounds by rubbing or grinding their bones together. These sounds are stridulatory. In Haemulon flavolineatum, the French grunt fish, as it produces a grunting noise by grinding its teeth together, especially when in distress. The grunts are at a frequency of around 700 Hz, and last approximately 47 milliseconds.[70] The longsnout seahorse, Hippocampus reidi produces two categories of sounds, 'clicks' and 'growls', by rubbing their coronet bone across the grooved section of their neurocranium.[71] Clicks are produced during courtship and feeding, and the frequencies of clicks were within the range of 50 Hz-800 Hz. The frequencies are at the higher end of the range during spawning, when the female and male fishes were less than fifteen centimeters apart. Growls are produced when the H. reidi are stressed. The 'growl' sounds consist of a series of sound pulses and are emitted simultaneously with body vibrations.[72]

Some fish species create noise by engaging specialized muscles that contract and cause swimbladder vibrations. Oyster toadfish produce loud grunts by contracting sonic muscles along the sides of the swim bladder.[73] Female and male toadfishes emit short-duration grunts, often as a fright response.[74] In addition to short-duration grunts, male toadfishes produce "boat whistle calls".[75] These calls are longer in duration, lower in frequency, and are primarily used to attract mates.[75] The sounds emitted by the O. tao have frequency range of 140 Hz to 260 Hz.[75] The frequencies of the calls depend on the rate at which the sonic muscles contract.[76][73]

The red drum, Sciaenops ocellatus, produces drumming sounds by vibrating its swimbladder. Vibrations are caused by the rapid contraction of sonic muscles that surround the dorsal aspect of the swimbladder. These vibrations result in repeated sounds with frequencies from 100 to >200 Hz. S. ocellatus produces different calls depending on the stimuli involved, such as courtship or a predator's attack. Females do not produce sounds, and lack sound-producing (sonic) muscles.[77]

Defense against disease

A cleaner fish, a Hawaiian cleaner wrasse, cleaning parasites from a white-spotted puffer

Like other animals, fish suffer from diseases and parasites. To prevent disease they have a variety of defenses. Non-specific defenses include the skin and scales, as well as the mucus layer secreted by the epidermis that traps and inhibits the growth of microorganisms. If pathogens breach these defenses, fish can develop an inflammatory response that increases blood flow to the infected region and delivers white blood cells that attempt to destroy pathogens. Specific defenses respond to particular pathogens recognised by the fish's body, i.e., an immune response.[78]

Some species use cleaner fish to remove external parasites. The best known of these are the bluestreak cleaner wrasses of coral reefs in the Indian and Pacific oceans. These small fish maintain cleaning stations where other fish congregate and perform specific movements to attract the attention of the cleaners.[79] Cleaning behaviors have been observed in a number of fish groups, including an interesting case between two cichlids of the same genus, Etroplus maculatus, the cleaner, and the much larger Etroplus suratensis.[80]

Immune organs vary by type of fish.[81] In the jawless fish (lampreys and hagfish), true lymphoid organs are absent. These fish rely on regions of lymphoid tissue within other organs to produce immune cells. For example, erythrocytes, macrophages and plasma cells are produced in the anterior kidney (or pronephros) and some areas of the gut (where granulocytes mature.) They resemble primitive bone marrow in hagfish. Cartilaginous fish (sharks and rays) have a more advanced immune system. They have three specialized organs that are unique to Chondrichthyes; the epigonal organs (lymphoid tissue similar to mammalian bone) that surround the gonads, the Leydig's organ within the walls of their esophagus, and a spiral valve in their intestine. These organs house typical immune cells (granulocytes, lymphocytes and plasma cells). They also possess an identifiable thymus and a well-developed spleen (their most important immune organ) where various lymphocytes, plasma cells and macrophages develop and are stored. Chondrostean fish (sturgeons, paddlefish, and bichirs) possess a major site for the production of granulocytes within a mass that is associated with the meninges (membranes surrounding the central nervous system.) Their heart is frequently covered with tissue that contains lymphocytes, reticular cells and a small number of macrophages. The chondrostean kidney is an important hemopoietic organ; where erythrocytes, granulocytes, lymphocytes and macrophages develop.

Like chondrostean fish, the major immune tissues of bony fish (or teleostei) include the kidney (especially the anterior kidney), which houses many different immune cells.[82] In addition, teleost fish possess a thymus, spleen and scattered immune areas within mucosal tissues (e.g. in the skin, gills, gut and gonads). Much like the mammalian immune system, teleost erythrocytes, neutrophils and granulocytes are believed to reside in the spleen whereas lymphocytes are the major cell type found in the thymus.[83][84] In 2006, a lymphatic system similar to that in mammals was described in one species of teleost fish, the zebrafish. Although not confirmed as yet, this system presumably will be where naive (unstimulated) T cells accumulate while waiting to encounter an antigen.[85]

B and T lymphocytes bearing immunoglobulins and T cell receptors, respectively, are found in all jawed fishes. Indeed, the adaptive immune system as a whole evolved in an ancestor of all jawed vertebrates.[86]

Conservation

The 2006 IUCN Red List names 1,173 fish species that are threatened with extinction.[87] Included are species such as Atlantic cod,[88] Devil's Hole pupfish,[89] coelacanths,[90] and great white sharks.[91] Because fish live underwater they are more difficult to study than terrestrial animals and plants, and information about fish populations is often lacking. However, freshwater fish seem particularly threatened because they often live in relatively small water bodies. For example, the Devil's Hole pupfish occupies only a single 3 by 6 metres (10 by 20 ft) pool.[92]

Overfishing

Collapse of the Atlantic northwest cod fishery

Overfishing is a major threat to edible fish such as cod and tuna.[93][94] Overfishing eventually causes population (known as stock) collapse because the survivors cannot produce enough young to replace those removed. Such commercial extinction does not mean that the species is extinct, merely that it can no longer sustain a fishery. A well-studied example of fishery collapse is the Pacific sardine Sadinops sagax caerulues fishery off the California coast. From a 1937 peak of 790,000 long tons (800,000 t) the catch steadily declined to only 24,000 long tons (24,000 t) in 1968, after which the fishery was no longer economically viable.[95]

Fisheries scientists and the fishing industry have different views on the resiliency of fisheries to intensive fishing. In places such as Scotland, Newfoundland, and Alaska the fishing industry is a major employer, so governments are predisposed to support it.[96][97] On the other hand, scientists and conservationists push for stringent protection, warning that many stocks could be wiped out within fifty years.[98][99]

Habitat destruction

A key stress on both freshwater and marine ecosystems is habitat degradation including water pollution, the building of dams, removal of water for use by humans, and the introduction of exotic species.[100] An example of a fish that has become endangered because of habitat change is the pallid sturgeon, a North American freshwater fish that lives in rivers damaged by human activity.[101]

Exotic species

Introduction of non-native species occurs in many habitats. The Mediterranean Sea has become a major 'hotspot' of exotic invaders since the opening of the Suez Canal in 1869. A thousand marine species of all sorts – fishes, seaweeds, invertebrates – originating from the Red Sea and more broadly from the Indo-Pacific have crossed the Canal from south to north to settle in the eastern Mediterranean Basin. Nowadays many of these tropical migrants, also called Lessepsian species, have extended their range towards the west, obviously favoured by the general warming of the Mediterranean. The resulting change in biodiversity is without precedent in human memory and is accelerating: a long-term cross-Basin survey engaged by the Mediterranean Science Commission recently documented that in just twenty years, from 2001 till 2021, no less than 107 alien fish species have reached the Mediterranean from both the tropical Atlantic and the Red Sea, which is more than the total recorded during the whole 130 preceding years.[102]

Another mode of introduction for marine species is transport across thousands of kms on ship hulls or in ballast waters. Examples abound of marine organisms being transported in ballast water, among them the invasive comb jelly Mnemiopsis leidyi, the dangerous bacterium Vibrio cholerae, or the fouling zebra mussel. The Mediterranean and Black Seas, with their high volume shipping from exotic harbors, are particularly impacted by this problem.[103]

Deliberate introductions of species with market potential are another frequent vector: one of the best studied examples is the introduction of the Nile perch into Lake Victoria in the 1960s. Nile perch gradually exterminated the lake's 500 endemic cichlid species. Some of them now survive in captive breeding programmes, but others are probably extinct.[104] Carp, snakeheads,[105] tilapia, European perch, brown trout, rainbow trout, and sea lampreys are other examples of fish that have caused problems by being introduced into alien environments.

Importance to humans

Economic

A trawler hauling in a large catch of cod, 2016

Throughout history, humans have used fish as a food source for dietary protein. Historically and today, most fish harvested for human consumption has come by means of catching wild fish. However, fish farming, which has been practiced since about 3,500 BCE in ancient China,[106] is becoming increasingly important in many nations. Overall, about one-sixth of the world's protein is estimated to be provided by fish.[107] That proportion is considerably elevated in some developing nations and regions heavily dependent on seafood. In a similar manner, fish have been tied to primary industry and associated food, feed, pharmaceutical production and service industries.

Catching fish for the purpose of food or sport is known as fishing, while the organized effort by humans to catch fish is called a fishery (which also describes the area where such enterprise operates). Fisheries are a huge global business and provide income for millions of people.[107] The annual yield from all fisheries worldwide is about 154 million tons,[108] with popular species including herring, cod, anchovy, tuna, flounder, and salmon. However, the term fishery is broadly applied, and includes more organisms than just fish, such as mollusks and crustaceans, which are often collectively called "shellfish" when used as food.

The Environmental Defense Fund (EDF) has a guide[109] to which fish are healthiest (or least safe) to eat, given the state of pollution in today's world, and also which fish are obtained in a way that does not lead towards extinction of the fish.

Recreation

Fish have been recognized as a source of beauty for almost as long as used for food, appearing in cave art, being raised as ornamental fish in ponds, and displayed in aquariums in homes, offices, or public settings. Recreational fishing is fishing primarily for pleasure or competition; it can be contrasted with commercial fishing, which is fishing for profit, or artisanal fishing, which is fishing primarily for food. The most common form of recreational fishing is done with a rod, reel, line, hooks, and any one of a wide range of baits. Recreational fishing is particularly popular in North America and Europe and state, provincial, and federal government agencies actively management target fish species.[110][111]

Culture

Fish themes have symbolic significance in many religions. In ancient Mesopotamia, fish offerings were made to the gods from the very earliest times.[112] Fish were also a major symbol of Enki, the god of water.[112] Fish frequently appear as filling motifs in cylinder seals from the Old Babylonian (c. 1830 BC – c. 1531 BC) and Neo-Assyrian (911–609 BC) periods.[112] Starting during the Kassite Period (c. 1600 BC – c. 1155 BC) and lasting until the early Persian Period (550–30 BC), healers and exorcists dressed in ritual garb resembling the bodies of fish.[112] During the Seleucid Period (312–63 BC), the legendary Babylonian culture hero Oannes, described by Berossus, was said to have dressed in the skin of a fish.[112] Fish were sacred to the Syrian goddess Atargatis[113] and, during her festivals, only her priests were permitted to eat them.[113]

In the Book of Jonah, the central figure, a prophet named Jonah, is swallowed by a giant fish after being thrown overboard by the crew of the ship he is travelling on.[114] Early Christians used the ichthys, a symbol of a fish, to represent Jesus,[113][115] because the Greek word for fish, ΙΧΘΥΣ Ichthys, could be used as an acronym for "Ίησοῦς Χριστός, Θεοῦ Υἱός, Σωτήρ" (Iesous Christos, Theou Huios, Soter), meaning "Jesus Christ, Son of God, Saviour".[113][115]

Among the deities said to take the form of a fish are Ika-Roa of the Polynesians, Dagon of various ancient Semitic peoples, the shark-gods of Hawaiʻi and Matsya of the Hindus. The astrological symbol Pisces is based on a constellation of the same name, but there is also a second fish constellation in the night sky, Piscis Austrinus.[116]

Fish feature prominently in art, in movies such as Finding Nemo and books such as The Old Man and the Sea. Large fish, particularly sharks, have frequently been the subject of horror movies and thrillers, notably the novel Jaws, in turn parodied in Shark Tale and Snakehead Terror. Piranhas are shown in a similar light to sharks in films such as Piranha; however, contrary to popular belief, the red-bellied piranha is actually a generally timid scavenger species that is unlikely to harm humans.[117]

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