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Dolphin
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Dolphins
A common bottlenose dolphin (Tursiops truncatus)
A common bottlenose dolphin (Tursiops truncatus)
Scientific classificationEdit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Infraorder: Cetacea
Parvorder: Odontoceti
Groups included
Cladistically included but traditionally excluded taxa

A dolphin is a common name used for some of the aquatic mammals in the cetacean clade Odontoceti, the toothed whales. Dolphins belong to the families Delphinidae (the oceanic dolphins), along with the river dolphin families Platanistidae (the Indian river dolphins), Iniidae (the New World river dolphins), Pontoporiidae (the brackish dolphins), and probably extinct Lipotidae (baiji or Chinese river dolphin). There are 40 extant species named as dolphins.

Dolphins range in size from the 1.7-metre-long (5 ft 7 in) and 50-kilogram (110-pound) Maui's dolphin to the 9.5 m (31 ft) and 10-tonne (11-short-ton) orca. Various species of dolphins exhibit sexual dimorphism where the males are larger than females. They have streamlined bodies and two limbs that are modified into flippers. Though not quite as flexible as seals, they are faster; some dolphins can briefly travel at speeds of 29 kilometres per hour (18 mph) or leap about 9 metres (30 ft).[1] Dolphins use their conical teeth to capture fast-moving prey. They have well-developed hearing which is adapted for both air and water; it is so well developed that some can survive even if they are blind.[citation needed] Some species are well adapted for diving to great depths. They have a layer of fat, or blubber, under the skin to keep warm in the cold water.

Dolphins are widespread. Most species prefer the warm waters of the tropic zones, but some, such as the right whale dolphin, prefer colder climates. Dolphins feed largely on fish and squid, but a few large-bodied dolphins, such as the orca, feed on large prey such as seals, sharks, and other dolphins. Male dolphins typically mate with multiple females every year, but females only mate every two to three years. Calves are typically born in the spring and summer months and females bear all the responsibility for raising them. Mothers of some species fast and nurse their young for a relatively long period of time.

Dolphins produce a variety of vocalizations, usually in the form of clicks and whistles.

Dolphins are sometimes hunted in places such as Japan, in an activity known as dolphin drive hunting. Besides drive hunting, they also face threats from bycatch, habitat loss, and marine pollution. Dolphins feature in various cultures worldwide, such as in art or folklore. Dolphins are sometimes kept in captivity within dolphinariums and trained to perform tricks; the most common dolphin species in captivity is the bottlenose dolphin, while there are around 60 orcas in captivity.

Etymology

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The name is originally from Greek δελφίς (delphís), "dolphin",[2] which was related to the Greek δελφύς (delphus), "womb".[2] The animal's name can therefore be interpreted as meaning "a 'fish' with a womb".[3] The name was transmitted via the Latin delphinus[4] (the romanization of the later Greek δελφῖνος – delphinos[2]), which in Medieval Latin became dolfinus and in Old French daulphin, which reintroduced the spelling ph into the word dolphin. The term mereswine ("sea pig") is also used.[5][6]

The term dolphin can be used to refer to most species in the family Delphinidae (oceanic dolphins) and the river dolphin families of Iniidae (South American river dolphins), Pontoporiidae (La Plata dolphin), Lipotidae (Yangtze river dolphin) and Platanistidae (Ganges river dolphin and Indus river dolphin).[7][8] Meanwhile, the mahi-mahi fish is called the dolphinfish.[9] In common usage, the term whale is used only for the larger cetacean species,[10] while the smaller ones with a beaked or longer nose are considered dolphins.[11] The name dolphin is used casually as a synonym for bottlenose dolphin, the most common and familiar species of dolphin.[12] There are six species of dolphins commonly thought of as whales, collectively known as blackfish: the orca, the melon-headed whale, the pygmy killer whale, the false killer whale, and the two species of pilot whales, all of which are classified under the family Delphinidae and qualify as dolphins.[13] Although the terms dolphin and porpoise are sometimes used interchangeably, porpoise usually refers to the Phocoenidae family, which have a shorter beak and spade-shaped teeth and differ in their behavior.[12]

A group of dolphins is called a school or a pod. Male dolphins are called bulls, females are called cows and young dolphins are called calves.[14]

Evolution

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Dolphins display convergent evolution with fish and aquatic reptiles.

Dolphins are descendants of land-dwelling mammals of the artiodactyl order (even-toed ungulates). They are related to the Indohyus, an extinct chevrotain-like ungulate, from which they split approximately 48 million years ago.[15][16]

The primitive cetaceans, or archaeocetes, first took to the sea approximately 49 million years ago and became fully aquatic by 5–10 million years later.[17]

Archaeoceti is a parvorder comprising ancient whales. These ancient whales are the predecessors of modern whales, stretching back to their first ancestor that spent their lives near (rarely in) the water. Likewise, the archaeocetes can be anywhere from near fully terrestrial, to semi-aquatic to fully aquatic, but what defines an archaeocete is the presence of visible legs or asymmetrical teeth.[18][19][20][21] Their features became adapted for living in the marine environment. Major anatomical changes include the hearing set-up that channeled vibrations from the jaw to the earbone which occurred with Ambulocetus 49 million years ago, a streamlining of the body and the growth of flukes on the tail which occurred around 43 million years ago with Protocetus, the migration of the nasal openings toward the top of the cranium and the modification of the forelimbs into flippers which occurred with Basilosaurus 35 million years ago, and the shrinking and eventual disappearance of the hind limbs which took place with the first odontocetes and mysticetes 34 million years ago.[22][23][24] The modern dolphin skeleton has two small, rod-shaped pelvic bones thought to be vestigial hind limbs. In October 2006, an unusual bottlenose dolphin was captured in Japan; it had small fins on each side of its genital slit, which scientists believe to be an unusually pronounced development of these vestigial hind limbs.[25]

Today, the closest living relatives of cetaceans are the hippopotamuses; these share a semi-aquatic ancestor that branched off from other artiodactyls some 60 million years ago.[26] Around 40 million years ago, a common ancestor between the two branched off into cetacea and anthracotheres; anthracotheres became extinct at the end of the Pleistocene two-and-a-half million years ago, eventually leaving only one surviving lineage: the two species of hippo.[27][28]

Anatomy

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The anatomy of a dolphin showing its skeleton, major organs, tail and body shape.

Dolphins have torpedo-shaped bodies with generally non-flexible necks, limbs modified into flippers, a tail fin, and bulbous heads. Dolphin skulls have small eye orbits, long snouts, and eyes placed on the sides of its head; they lack external ear flaps. Dolphins range in size from the 1.7 m (5 ft 7 in) long and 50 kg (110 lb) Maui's dolphin to the 9.5 m (31 ft 2 in) and 10 t (11 short tons) orca. Overall, they tend to be dwarfed by other Cetartiodactyls. Several species have female-biased sexual dimorphism, with the females being larger than the males.[29][30]

Dolphins have conical teeth, as opposed to porpoises' spade-shaped teeth. These conical teeth are used to catch swift prey such as fish, squid or large mammals, such as seals.[30]

Breathing involves expelling stale air from their blowhole, in an upward blast, which may be visible in cold air, followed by inhaling fresh air into the lungs. Dolphins have rather small, unidentifiable spouts.[30][31]

All dolphins have a thick layer of blubber, thickness varying on climate. This blubber can help with buoyancy, protection to some extent as predators would have a hard time getting through a thick layer of fat, and energy for leaner times; the primary usage for blubber is insulation from the harsh climate. Calves, generally, are born with a thin layer of blubber, which develops at different paces depending on the habitat.[30][32]

Dolphins have a two-chambered[33] or three-chambered[34] stomach that is similar in cellular structure to that of terrestrial carnivores. They have fundic and pyloric chambers.[33]

Dolphins' reproductive organs are located inside the body, with genital slits on the ventral (belly) side. Males have two slits, one concealing the penis and one further behind for the anus.[35] Females have one genital slit, housing the vagina and the anus, with a mammary slit on either side.[36][37][38]

Integumentary system

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The integumentary system is an organ system mostly consisting of skin, hair, nails and endocrine glands. The skin of dolphins is specialized to satisfy specific requirements, including protection, fat storage, heat regulation, and sensory perception. The skin of a dolphin is made up of two parts: the epidermis and the blubber, which consists of two layers including the dermis and subcutis.[39]

The dolphin's skin is known to have a smooth rubber texture and is without hair and glands, except mammary glands. At birth, a newborn dolphin has hairs lined up in a single band on both sides of the rostrum, which is their jaw, and usually has a total length of 16–17 cm .[39] The epidermis is characterized by the lack of keratin and by a prominent intertwine of epidermal rete pegs and long dermal papillae.[39] The epidermal rete pegs are the epithelial extensions that project into the underlying connective tissue in both skin and mucous membranes. The dermal papillae are finger-like projections that help adhesion between the epidermal and dermal layers, as well as providing a larger surface area to nourish the epidermal layer.[40] The thickness of a dolphin's epidermis varies, depending on species and age.

Blubber

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Blubber is found within the dermis and subcutis layer. The dermis blends gradually with the adipose layer, which is known as fat, because the fat may extend up to the epidermis border and collagen fiber bundles extend throughout the whole subcutaneous blubber which is fat found under the skin.[39] The thickness of the subcutaneous blubber or fat depends on the dolphin's health, development, location, reproductive state, and how well it feeds. This fat is thickest on the dolphin's back and belly. Most of the dolphin's body fat is accumulated in a thick layer of blubber. Blubber differs from fat in that, in addition to fat cells, it contains a fibrous network of connective tissue.[41]

The blubber functions to streamline the body and to form specialized locomotor structures such as the dorsal fin, propulsive fluke blades and caudal keels.[39] There are many nerve endings that resemble small, onion-like configurations that are present in the superficial portion of the dermis. Mechanoreceptors are found within the interlocks of the epidermis with dermal ridges. There are nerve fibers in the dermis that extend to the epidermis. These nerve endings are known to be highly proprioceptive, which explains sensory perception.[39] Proprioception, which is also known as kinesthesia, is the body's ability to sense its location, movements and actions. Dolphins are sensitive to vibrations and small pressure changes.[42] Blood vessels and nerve endings can be found within the dermis. There is a plexus of parallel running arteries and veins in the dorsal fin, fluke, and flippers.[39] The blubber manipulates the blood vessels to help the dolphin stay warm. When the temperature drops, the blubber constricts the blood vessels to reduce blood flow in the dolphin.[43] This allows the dolphin to spend less energy heating its own body, ultimately keeping the animal warmer without burning energy as quick. In order to release heat, the heat must pass the blubber layer. There are thermal windows that lack blubber, are not fully insulated and are somewhat thin and highly vascularized, including the dorsal fin, flukes, and flippers.[44] These thermal windows are a good way for dolphins to get rid of excess heat if overheating. Additionally in order to conserve heat, dolphins use countercurrent heat exchange. Blood flows in different directions in order for heat to transfer across membranes. Heat from warm blood leaving the heart will heat up the cold blood that is headed back to the heart from the extremities, meaning that the heart always has warm blood and it decreases the heat lost to the water in those thermal windows.[44]

Bottlenose dolphins swimming and jumping in captivity, 2025

Locomotion

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Dolphins have two pectoral flippers, each containing four digits, a boneless dorsal fin for stability, and a fluke for propulsion. Although dolphins do not possess external hind limbs, some possess discrete rudimentary appendages, which may contain feet and digits. Orcas are fast swimmers in comparison to seals which typically cruise at 9–28 km/h (5.6–17.4 mph); the orca, in comparison, can travel at speeds up to 55.5 km/h (34.5 mph).[citation needed] A study of a Pacific white-sided dolphin in an aquarium found fast burst acceleration, with the individual being able with 5 strokes (2.5 fluke beats) to go from 5.0 m s-1 to 8.7 m s-1 in 0.7 seconds.[45]

The fusing of the neck vertebrae, while increasing stability when swimming at high speeds, decreases flexibility, which means most dolphins are unable to turn their heads.[46][47] River dolphins have non-fused neck vertebrae and can turn their heads up to 90°.[48] Dolphins swim by moving their fluke and rear body vertically, while their flippers are mainly used for steering. Some species porpoise out of the water, which allows them to travel faster. Their skeletal anatomy allows them to be fast swimmers. All species have a dorsal fin to prevent themselves from involuntarily spinning in the water.[30][32]

Some dolphins are adapted for diving to great depths. In addition to their streamlined bodies, some can selectively slow their heart rate to conserve oxygen.[49][50] Some can also re-route blood from tissue tolerant of water pressure to the heart, brain and other organs. Their hemoglobin and myoglobin store oxygen in body tissues, and they have twice as much myoglobin as hemoglobin.[51]

Senses

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Biosonar by cetaceans

Diagram illustrating sound generation, propagation, and reception in a toothed whale. Outgoing sounds are in cyan and incoming ones are in green

A dolphin ear has specific adaptations to the marine environment. In humans, the middle ear works as an impedance equalizer between the outside air's low impedance and the cochlear fluid's high impedance. In dolphins, and other marine mammals, there is no great difference between the outer and inner environments. Instead of sound passing through the outer ear to the middle ear, dolphins receive sound through the throat, from which it passes through a low-impedance fat-filled cavity to the inner ear. The ear is acoustically isolated from the skull by air-filled sinus pockets, which allow for greater directional hearing underwater.[52]

Dolphins generate sounds independently of respiration using recycled air that passes through air sacs and phonic (alternatively monkey) lips. Integral to the lips are oil-filled organs called dorsal bursae that have been suggested to be homologous to the sperm whale's spermaceti organ.[53] High-frequency clicks pass through the sound-modifying organs of the extramandibular fat body, intramandibular fat body and the melon. This melon consists of fat, and the skull of any such creature containing a melon will have a large depression. This allows dolphins to use echolocation for orientation.[30][54][55][56][57] Though most dolphins do not have hair, they do have hair follicles that may perform some sensory function.[58] Beyond locating an object, echolocation also provides the animal with an idea on an object's shape and size, though how exactly this works is not yet understood.[59] The small hairs on the rostrum of the boto (river dolphins of South America) are believed to function as a tactile sense, possibly to compensate for the boto's poor eyesight.[60]

A dolphin eye is relatively small for its size, yet they do retain a good degree of eyesight. As well as this, the eyes of a dolphin are placed on the sides of its head, so their vision consists of two fields, rather than a binocular view like humans have. When dolphins surface, their lens and cornea correct the nearsightedness that results from the water's refraction of light. Their eyes contain both rod and cone cells, meaning they can see in both dim and bright light, but they have far more rod cells than they do cone cells. They lack short wavelength sensitive visual pigments in their cone cells, indicating a more limited capacity for color vision than most mammals.[61] Most dolphins have slightly flattened eyeballs, enlarged pupils (which shrink as they surface to prevent damage), slightly flattened corneas and a tapetum lucidum (eye tissue behind the retina); these adaptations allow for large amounts of light to pass through the eye and, therefore, a very clear image of the surrounding area. They also have glands on the eyelids and outer corneal layer that act as protection for the cornea.[54]

The olfactory lobes and nerve are absent in dolphins, suggesting that they have no sense of smell.[54]

Dolphins are not thought to have a good sense of taste, as their taste buds are atrophied or missing altogether. Some have preferences for different kinds of fish, indicating some ability to taste.[54]

Intelligence

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The face of a common bottlenose dolphin

Dolphins are known to teach, learn, cooperate, scheme, and grieve.[62] The neocortex of many species is home to elongated spindle neurons that, prior to 2007, were known only in hominids.[63] In humans, these cells are involved in social conduct, emotions, judgment, and theory of mind.[64] Cetacean spindle neurons are found in areas of the brain that are analogous to where they are found in humans, suggesting that they perform a similar function.[65]

Brain size was previously considered a major indicator of the intelligence of an animal. Since most of the brain is used for maintaining bodily functions, greater ratios of brain to body mass may increase the amount of brain mass available for more complex cognitive tasks. Allometric analysis indicates that mammalian brain size scales at approximately the two-thirds or three-fourths exponent of the body mass. [clarification needed][66] Comparison of a particular animal's brain size with the expected brain size based on such allometric analysis provides an encephalization quotient that can be used as another indication of animal intelligence. Orcas have the second largest brain mass of any animal on earth, next to the sperm whale.[67] The brain to body mass ratio in some is second only to humans.[68]

Self-awareness is seen, by some, to be a sign of highly developed, abstract thinking. Self-awareness, though not well-defined scientifically, is believed to be the precursor to more advanced processes like meta-cognitive reasoning (thinking about thinking) that are typical of humans. Research in this field has suggested that cetaceans, among others, possess self-awareness.[69] The most widely used test for self-awareness in animals is the mirror test in which a mirror is introduced to an animal, and the animal is then marked with a temporary dye. If the animal then goes to the mirror in order to view the mark, it has exhibited strong evidence of self-awareness.[70]

Some disagree with these findings, arguing that the results of these tests are open to human interpretation and susceptible to the Clever Hans effect. This test is much less definitive than when used for primates, because primates can touch the mark or the mirror, while cetaceans cannot, making their alleged self-recognition behavior less certain. Skeptics argue that behaviors that are said to identify self-awareness resemble existing social behaviors, and so researchers could be misinterpreting self-awareness for social responses to another individual. The researchers counter-argue that the behaviors shown are evidence of self-awareness, as they are very different from normal responses to another individual. Whereas apes can merely touch the mark on themselves with their fingers, cetaceans show less definitive behavior of self-awareness; they can only twist and turn themselves to observe the mark.[70]

In 1995, Marten and Psarakos used television to test dolphin self-awareness.[71] They showed dolphins real-time video of themselves, video of another dolphin and recorded footage. They concluded that their evidence suggested self-awareness rather than social behavior. While this particular study has not been repeated since then, dolphins have since passed the mirror test.[70] Some researchers have argued that evidence for self-awareness has not been convincingly demonstrated.[72]

Behavior

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A pod of Indo-Pacific bottlenose dolphins in the Red Sea

Socialization

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Dolphins surfing at Snapper Rocks, Queensland, Australia

Dolphins are highly social animals, often living in pods of up to a dozen individuals, though pod sizes and structures vary greatly between species and locations. In places with a high abundance of food, pods can merge temporarily, forming a superpod; such groupings may exceed 1,000 dolphins. Membership in pods is not rigid; interchange is common. They establish strong social bonds, and will stay with injured or ill members, helping them to breathe by bringing them to the surface if needed.[73] This altruism does not appear to be limited to their own species. The dolphin Moko in New Zealand has been observed guiding a female pygmy sperm whale together with her calf out of shallow water where they had stranded several times.[74] They have also been seen protecting swimmers from sharks by swimming circles around the swimmers[75][76] or charging the sharks to make them go away.

Dolphins communicate using a variety of clicks, whistle-like sounds and other vocalizations. Dolphins also use nonverbal communication by means of touch and posturing.[77]

Dolphins also display culture, something long believed to be unique to humans (and possibly other primate species). In May 2005, a discovery in Australia found Indo-Pacific bottlenose dolphins (Tursiops aduncus) teaching their young to use tools. They cover their snouts with sponges to protect them while foraging. This knowledge is mostly transferred by mothers to daughters, unlike simian primates, where knowledge is generally passed on to both sexes. Using sponges as mouth protection is a learned behavior.[78] Another learned behavior was discovered among river dolphins in Brazil, where some male dolphins use weeds and sticks as part of a sexual display.[79]

Forms of care-giving between fellows and even for members of different species[80] (see Moko (dolphin)) are recorded in various species – such as trying to save weakened fellows[81] or female pilot whales holding up dead calves for long periods.

Dolphins engage in acts of aggression towards each other. The older a male dolphin is, the more likely his body is to be covered with bite scars. Male dolphins can get into disputes over companions and females. Acts of aggression can become so intense that targeted dolphins sometimes go into exile after losing a fight.

Male bottlenose dolphins have been known to engage in infanticide. Dolphins have also been known to kill porpoises (porpicide) for reasons which are not fully understood, as porpoises generally do not share the same diet as dolphins and are therefore not competitors for food supplies.[82][83] The Cornwall Wildlife Trust records about one such death a year. Possible explanations include misdirected infanticide, misdirected sexual aggression or play behaviour.[84]

Reproduction and sexuality

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A skin-skeletal preparation.

Dolphin copulation happens belly to belly; though many species engage in lengthy foreplay, the actual act is usually brief, but may be repeated several times within a short timespan.[85] The gestation period varies with species; for the small tucuxi dolphin, this period is around 11 to 12 months,[86] while for the orca, the gestation period is around 17 months.[87] Typically dolphins give birth to a single calf, which is, unlike most other mammals, born tail first in most cases.[88] They usually become sexually active at a young age, even before reaching sexual maturity.[85] The age of sexual maturity varies by species and sex.[89]

Dolphins are known to display non-reproductive sexual behavior, engaging in masturbation,[90] stimulation of the genital area of other individuals using the rostrum or flippers, and homosexual contact.[85][91][92]

Various species of dolphin have been known to engage in sexual behavior including copulation with dolphins of other species, and occasionally exhibit sexual behavior towards other animals, including humans.[93][94] Sexual encounters may be violent, with male bottlenose dolphins sometimes showing aggressive behavior towards both females and other males.[95] Male dolphins may also work together and attempt to herd females in estrus, keeping the females by their side by means of both physical aggression and intimidation, to increase their chances of reproductive success.[96]

Hybridization

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In 1933, three hybrid dolphins beached off the Irish coast; they were hybrids between Risso's and bottlenose dolphins.[97] This mating was later repeated in captivity, producing a hybrid calf. In captivity, a bottlenose and a rough-toothed dolphin produced hybrid offspring.[98] A common-bottlenose hybrid lives at SeaWorld California.[99] Other dolphin hybrids live in captivity around the world or have been reported in the wild, such as a bottlenose-Atlantic spotted hybrid.[100] The best known hybrid is the wholphin, a false killer whale-bottlenose dolphin hybrid. The wholphin is a fertile hybrid. Two wholphins currently live at the Sea Life Park in Hawaii; the first was born in 1985 from a male false killer whale and a female bottlenose. Wholphins have also been observed in the wild.[101]

Sleeping

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Sleeping dolphin in captivity: a tail kick reflex keeps the dolphin's blowhole above the water.

Generally, dolphins sleep with only one brain hemisphere in slow-wave sleep at a time, thus maintaining enough consciousness to breathe and to watch for possible predators and other threats. Sleep stages earlier in sleep can occur simultaneously in both hemispheres.[102][103][104] In captivity, dolphins seemingly enter a fully asleep state where both eyes are closed and there is no response to mild external stimuli. In this case, respiration is automatic; a tail kick reflex keeps the blowhole above the water if necessary. Anesthetized dolphins initially show a tail kick reflex.[105] Though a similar state has been observed with wild sperm whales, it is not known if dolphins in the wild reach this state.[106] The Indus river dolphin has a sleep method that is different from that of other dolphin species. Living in water with strong currents and potentially dangerous floating debris, it must swim continuously to avoid injury. As a result, this species sleeps in very short bursts which last between 4 and 60 seconds.[107]

Feeding

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There are various feeding methods among and within species, some apparently exclusive to a single population. Fish and squid are the main food, but the false killer whale and the orca also feed on other marine mammals. Orcas on occasion also hunt whale species larger than themselves.[108] Different breeds of dolphins vary widely in the number of teeth they possess. The orca usually carries 40–56 teeth while the popular bottlenose dolphin has anywhere from 72 to 116 conical teeth and its smaller cousin the common dolphin has 188–268 teeth: the number of teeth that an individual carries varies widely between within a single species. Hybrids between common and bottlenose bred in captivity had a number of teeth intermediate between that of their parents.

One common feeding method is herding, where a pod squeezes a school of fish into a small volume, known as a bait ball. Individual members then take turns plowing through the ball, feeding on the stunned fish.[108] Corralling is a method where dolphins chase fish into shallow water to catch them more easily.[108] Orcas and bottlenose dolphins have also been known to drive their prey onto a beach to feed on it, a behaviour known as beach or strand feeding.[109][110] Some species also whack fish with their flukes, stunning them and sometimes knocking them out of the water.[108]

Reports of cooperative human-dolphin fishing date back to the ancient Roman author and natural philosopher Pliny the Elder.[111] A modern human-dolphin partnership currently operates in Laguna, Santa Catarina, Brazil. Here, dolphins drive fish towards fishermen waiting along the shore and signal the men to cast their nets. The dolphins' reward is the fish that escape the nets.[112][113]

In Shark Bay, Australia, dolphins catch fish by trapping them in huge conch shells.[114] In "shelling", a dolphin brings the shell to the surface and shakes it, so that fish sheltering within fall into the dolphin's mouth. From 2007 to 2018, in 5,278 encounters with dolphins, researchers observed 19 dolphins shelling 42 times. The behavior spreads mainly within generations, rather than being passed from mother to offspring.

Vocalization

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Spectrogram of dolphin vocalizations. Whistles, whines, and clicks are visible as upside down V's, horizontal striations, and vertical lines, respectively.

Dolphins are capable of making a broad range of sounds using nasal airsacs located just below the blowhole. Roughly three categories of sounds can be identified: frequency modulated whistles, burst-pulsed sounds, and clicks. Dolphins communicate with whistle-like sounds produced by vibrating connective tissue, similar to the way human vocal cords function,[115] and through burst-pulsed sounds, though the nature and extent of that ability is not known. The clicks are directional and are for echolocation, often occurring in a short series called a click train. The click rate increases when approaching an object of interest. Dolphin echolocation clicks are amongst the loudest sounds made by marine animals.[116]

Bottlenose dolphins have been found to have signature whistles, a whistle that is unique to a specific individual. These whistles are used in order for dolphins to communicate with one another by identifying an individual. It can be seen as the dolphin equivalent of a name for humans.[117] These signature whistles are developed during a dolphin's first year; it continues to maintain the same sound throughout its lifetime.[118] In order to obtain each individual whistle sound, dolphins undergo vocal production learning. This consists of an experience with other dolphins that modifies the signal structure of an existing whistle sound. An auditory experience influences the whistle development of each dolphin. Dolphins are able to communicate to one another by addressing another dolphin through mimicking their whistle. The signature whistle of a male bottlenose dolphin tends to be similar to that of his mother, while the signature whistle of a female bottlenose dolphin tends to be more distinguishing.[119] Bottlenose dolphins have a strong memory when it comes to these signature whistles, as they are able to relate to a signature whistle of an individual they have not encountered for over twenty years.[120] Research done on signature whistle usage by other dolphin species is relatively limited. The research on other species done so far has yielded varied outcomes and inconclusive results.[121][122][123][124]

Because dolphins generally associate in groups, communication is necessary. Signal masking is when other similar sounds (conspecific sounds) interfere with the original acoustic sound.[125] In larger groups, individual whistle sounds are less prominent. Dolphins tend to travel in pods, upon which there are groups of dolphins that range from a few to many. Although they are traveling in these pods, the dolphins do not necessarily swim right next to each other. Rather, they swim within the same general vicinity. In order to prevent losing one of their pod members, there are higher whistle rates. Because their group members were spread out, this was done in order to continue traveling together.

Jumping and playing

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Pacific white-sided dolphins porpoising.

Dolphins frequently leap above the water surface, this being done for various reasons. When travelling, jumping can save the dolphin energy as there is less friction while in the air.[126] This type of travel is known as porpoising.[126] Other reasons include orientation, social displays, fighting, non-verbal communication, entertainment and attempting to dislodge parasites.[127][128]

Dolphins show various types of playful behavior, often including objects, self-made bubble rings, other dolphins or other animals.[8][129][130] When playing with objects or small animals, common behavior includes carrying the object or animal along using various parts of the body, passing it along to other members of the group or taking it from another member, or throwing it out of the water.[129] Dolphins have also been observed harassing animals in other ways, for example by dragging birds underwater without showing any intent to eat them.[129] Playful behaviour that involves another animal species with active participation of the other animal has also been observed. Playful dolphin interactions with humans are the most obvious examples, followed by those with humpback whales and dogs.[131][132]

Juvenile dolphins off the coast of Western Australia have been observed chasing, capturing, and chewing on blowfish.[133] While some reports state that the dolphins are becoming intoxicated on the tetrodotoxin in the fishes' skin,[134] other reports have characterized this behavior as the normal curiosity and exploration of their environment in which dolphins engage.[135]

Tail-walking

[edit]

Although this behaviour is highly unusual in wild dolphins, several Indo-Pacific bottlenose dolphins (Tursiops aduncus) of the Port River, north of Adelaide, South Australia, have been seen to have exhibit "tail-walking".[136][137] This activity mimicks a standing posture, using the tail to run backwards along the water.[138] To perform this movement, the dolphin "forces the majority of its body vertically out of the water and maintains the position by vigorously pumping its tail".[137]

This started in 1988 when a female named Billie was rescued after becoming trapped in a polluted marina,[139] and spent two weeks recuperating with captive dolphins. Billie had previously been observed swimming and frolicking with racehorses exercising in the Port River in the 1980s. After becoming trapped in a reedy estuary further down the coast, she was rescued and placed with several captive dolphins at a marine park to recuperate. There she observed the captive dolphins performing tail-walking.[138] After being returned to the Port River, she continued to perform this trick, and another dolphin, Wave, copied her. Wave, a very active tail-walker, passed on the skill to her daughters, Ripple and Tallula.[136]

After Billie's premature death, Wave started tail-walking much more frequently, and other dolphins in the group were observed also performing the behaviour.[137] In 2011, up to 12 dolphins were observed tail-walking, but only females appeared to learn the skill.[140] In October 2021, a dolphin was observed tail-walking over a number of hours.[139]

Scientists have found the spread of this behaviour, through up to two generations, surprising, as it brings no apparent advantage, and is very energy-consuming.[140] A 2018 study by Mike Rossley et al. suggested:[136]

Social learning is the most likely mechanism for the introduction and spread of this unusual behaviour, which has no known adaptive function. These observations demonstrate the potential strength of the capacity for spontaneous imitation in bottlenose dolphins, and help explain the origin and spread of foraging specializations observed in multiple populations of this genus.

Threats

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Lesions in the dorsal fin of a bottlenose dolphin caused by lobomycosis, a fungal infection of the skin.

Dolphins have few marine enemies. Some species or specific populations have none, making them apex predators. For most of the smaller species of dolphins, only a few of the larger sharks, such as the bull shark, dusky shark, tiger shark and great white shark, are a potential risk, especially for calves.[141] Some of the larger dolphin species, especially orcas, may also prey on smaller dolphins, but this seems rare.[142] Dolphins also suffer from a wide variety of diseases and parasites.[143][144] The Cetacean morbillivirus in particular has been known to cause regional epizootics often leaving hundreds of animals of various species dead.[145][146] Symptoms of infection are often a severe combination of pneumonia, encephalitis and damage to the immune system, which greatly impair the cetacean's ability to swim and stay afloat unassisted.[147][148] A study at the U.S. National Marine Mammal Foundation revealed that dolphins, like humans, develop a natural form of type 2 diabetes which may lead to a better understanding of the disease and new treatments for both humans and dolphins.[149]

Dolphins can tolerate and recover from extreme injuries such as shark bites although the exact methods used to achieve this are not known. The healing process is rapid and even very deep wounds do not cause dolphins to hemorrhage to death. Furthermore, even gaping wounds restore in such a way that the animal's body shape is restored, and infection of such large wounds seems rare.[150]

A study published in the journal Marine Mammal Science suggests that at least some dolphins survive shark attacks using everything from sophisticated combat moves to teaming up against the shark.[151][152][153]

Humans

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Rows of dead dolphin lying on concrete
Dead Atlantic white-sided dolphins in Hvalba on the Faroe Islands, killed in a drive hunt.

Some dolphin species are at risk of extinction, especially some river dolphin species such as the Amazon river dolphin, and the Ganges and Yangtze river dolphin, which are critically or seriously endangered. A 2006 survey found no individuals of the Yangtze river dolphin. The species now appears to be functionally extinct.[154]

Pesticides, heavy metals, plastics, and other industrial and agricultural pollutants that do not disintegrate rapidly in the environment concentrate in predators such as dolphins.[155] Injuries or deaths due to collisions with boats, especially their propellers, are also common.

Various fishing methods, most notably purse seine fishing for tuna and the use of drift and gill nets, unintentionally kill many dolphins.[156] Accidental by-catch in gill nets and incidental captures in antipredator nets that protect marine fish farms are common and pose a risk for mainly local dolphin populations.[157][158] In some parts of the world, such as Taiji in Japan and the Faroe Islands, dolphins are traditionally considered food and are killed in harpoon or drive hunts.[159] Dolphin meat is high in mercury and may thus pose a health danger to humans when consumed.[160]

Queensland's shark culling program, which has killed roughly 50,000 sharks since 1962, has also killed thousands of dolphins as bycatch.[161][162] "Shark control" programs in both Queensland and New South Wales use shark nets and drum lines, which entangle and kill dolphins.[163] Queensland's "shark control" program has killed more than 1,000 dolphins in recent years,[162] and at least 32 dolphins have been killed in Queensland since 2014.[164] A shark culling program in KwaZulu-Natal has killed at least 2,310 dolphins.[165]

Dolphin safe labels attempt to reassure consumers that fish and other marine products have been caught in a dolphin-friendly way. The earliest campaigns with "dolphin safe" labels were initiated in the 1980s as a result of cooperation between marine activists and the major tuna companies, and involved decreasing incidental dolphin kills by up to 50% by changing the type of nets used to catch tuna. The dolphins are netted only while fishermen are in pursuit of smaller tuna. Albacore are not netted this way, making albacore the only truly dolphin-safe tuna.[166] Loud underwater noises, such as those resulting from naval sonar use, live firing exercises, and certain offshore construction projects such as wind farms, may be harmful to dolphins, increasing stress, damaging hearing, and causing decompression sickness by forcing them to surface too quickly to escape the noise.[167][168]

Dolphins and other smaller cetaceans are also hunted in an activity known as dolphin drive hunting. This is accomplished by driving a pod together with boats and usually into a bay or onto a beach. Their escape is prevented by closing off the route to the ocean with other boats or nets. Dolphins are hunted this way in several places around the world, including the Solomon Islands, the Faroe Islands, Peru, and Japan, the most well-known practitioner of this method. By numbers, dolphins are mostly hunted for their meat, though some end up in dolphinariums. Despite the controversial nature of the hunt resulting in international criticism, and the possible health risk that the often polluted meat causes, thousands of dolphins are caught in drive hunts each year.

Impacts of climate change

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Dolphins are marine mammals with broad geographic extent, making them susceptible to climate change in various ways. The most common effect of climate change on dolphins is the increasing water temperatures across the globe.[169] This has caused a large variety of dolphin species to experience range shifts, in which the species move from their typical geographic region to cooler waters.[170][171] Another side effect of increasing water temperatures is the increase in harmful algae blooms, which has caused a mass die-off of bottlenose dolphins.[169]

In California, the 1982–83 El Niño warming event caused the near-bottom spawning market squid to leave southern California, which caused their predator, the pilot whale, to also leave. As the market squid returned six years later, Risso's dolphins came to feed on the squid. Bottlenose dolphins expanded their range from southern to central California, and stayed even after the warming event subsided.[170] The Pacific white-sided dolphin has had a decline in population in the southwest Gulf of California, the southern boundary of their distribution. In the 1980s they were abundant with group sizes up to 200 across the entire cool season. Then, in the 2000s, only two groups were recorded with sizes of 20 and 30, and only across the central cool season. This decline was not related to a decline of other marine mammals or prey, so it was concluded to have been caused by climate change as it occurred during a period of warming. Additionally, the Pacific white-sided dolphin had an increase in occurrence on the west coast of Canada from 1984 to 1998.[171]

In the Mediterranean, sea surface temperatures have increased, as well as salinity, upwelling intensity, and sea levels. Because of this, prey resources have been reduced causing a steep decline in the short-beaked common dolphin Mediterranean subpopulation, which was deemed endangered in 2003. This species now only exists in the Alboran Sea, due to its high productivity, distinct ecosystem, and differing conditions from the rest of the Mediterranean.[172]

In northwest Europe, many dolphin species have experienced range shifts from the region's typically colder waters. Warm water dolphins, like the short-beaked common dolphin and striped dolphin, have expanded north of western Britain and into the northern North Sea, even in the winter, which may displace the white-beaked and Atlantic white-sided dolphin that are in that region. The white-beaked dolphin has shown an increase in the southern North Sea since the 1960s because of this. The rough-toothed dolphin and Atlantic spotted dolphin may move to northwest Europe.[169] In northwest Scotland, white-beaked dolphins (local to the colder waters of the North Atlantic) have decreased while common dolphins (local to warmer waters) have increased from 1992 to 2003.[173] Additionally, Fraser's dolphin, found in tropical waters, was recorded in the UK for the first time in 1996.[169]

River dolphins are highly affected by climate change as high evaporation rates, increased water temperatures, decreased precipitation, and increased acidification occur.[170][174] River dolphins typically have a higher densities when rivers have a lox index of freshwater degradation and better water quality. [further explanation needed][174] Specifically looking at the Ganges river dolphin, the high evaporation rates and increased flooding on the plains may lead to more human river regulation, decreasing the dolphin population.[170]

As warmer waters lead to a decrease in dolphin prey, this led to other causes of dolphin population decrease. In the case of bottlenose dolphins, mullet populations decrease due to increasing water temperatures, which leads to a decrease in the dolphins' health and thus their population.[170] At the Shark Bay World Heritage Area in Western Australia, the local Indo-Pacific bottlenose dolphin population had a significant decline after a marine heatwave in 2011. This heatwave caused a decrease in prey, which led to a decline in dolphin reproductive rates as female dolphins could not get enough nutrients to sustain a calf.[175] The resultant decrease in fish population due to warming waters has also influenced humans to see dolphins as fishing competitors or even bait. Humans use dusky dolphins as bait or are killed off because they consume the same fish humans eat and sell for profit.[170] In the central Brazilian Amazon alone, approximately 600 pink river dolphins are killed each year to be used as bait.[174]

Relationships with humans

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In history and religion

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Fresco of dolphins, c. 1600 BC, from Knossos, Crete
Silver stater from Tarentum c. 290 BC showing Phalanthos riding a dolphin on one side and a rider with a shield decorated with a dolphin on the other side
Vessel in form of orca, Nazca culture, circa 200 AD. American Museum of Natural History collections.

Dolphins have long played a role in human culture.

In Greek myths, dolphins were seen invariably as helpers of humankind. Dolphins also seem to have been important to the Minoans, judging by artistic evidence from the ruined palace at Knossos. During the 2009 excavations of a major Mycenaean city at Iklaina, a striking fragment of a wall painting came to light, depicting a ship with three human figures and dolphins. Dolphins are common in Greek mythology, and many coins from ancient Greece have been found which feature a man, a boy or a deity riding on the back of a dolphin.[176] The Ancient Greeks welcomed dolphins; spotting dolphins riding in a ship's wake was considered a good omen.[177] In both ancient and later art, Cupid is often shown riding a dolphin. A dolphin rescued the poet Arion from drowning and carried him safe to land, at Cape Matapan, a promontory forming the southernmost point of the Peloponnesus. There was a temple to Poseidon and a statue of Arion riding the dolphin.[178]

The Greeks reimagined the Phoenician god Melqart as Melikertês (Melicertes) and made him the son of Athamas and Ino. He drowned but was transfigured as the marine deity Palaemon, while his mother became Leucothea. (cf Ino.) At Corinth, he was so closely connected with the cult of Poseidon that the Isthmian Games, originally instituted in Poseidon's honor, came to be looked upon as the funeral games of Melicertes. Phalanthus was another legendary character brought safely to shore (in Italy) on the back of a dolphin, according to Pausanias.

Dionysus was once captured by Etruscan pirates who mistook him for a wealthy prince they could ransom. After the ship set sail Dionysus invoked his divine powers, causing vines to overgrow the ship where the mast and sails had been. He turned the oars into serpents, so terrifying the sailors that they jumped overboard, but Dionysus took pity on them and transformed them into dolphins so that they would spend their lives providing help for those in need. Dolphins were also the messengers of Poseidon and sometimes did errands for him as well. Dolphins were sacred to both Aphrodite and Apollo.

"Dolfin" was the name of an aristocratic family in the maritime Republic of Venice, whose most prominent member was the 13th-century Doge Giovanni Dolfin.

In Hindu mythology the Ganges river dolphin is associated with Ganga, the deity of the Ganges river. The dolphin is said to be among the creatures which heralded the goddess' descent from the heavens and her mount, the Makara, is sometimes depicted as a dolphin.[179]

The Boto, a species of river dolphin that resides in the Amazon River, are believed to be shapeshifters, or encantados, who are capable of having children with human women.

There are comparatively few surviving myths of dolphins in Polynesian cultures, in spite of their maritime traditions and reverence of other marine animals such as sharks and seabirds; unlike these, they are more often perceived as food than as totemic symbols. Dolphins are most clearly represented in Rapa Nui Rongorongo, and in the traditions of the Caroline Islands they are depicted similarly to the Boto, being sexually active shapeshifters.[180]

Heraldry

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Coat of arms of the Dauphiné, France, featuring a stylised heraldic dolphin

Dolphins are also used as symbols, for instance in heraldry. When heraldry developed in the Middle Ages, little was known about the biology of the dolphin and it was often depicted as a sort of fish. The stylised heraldic dolphin still conventionally follows this tradition, sometimes showing the dolphin skin covered with fish scales.

A well-known historical example was the coat of arms of the former province of the Dauphiné in southern France, from which were derived the arms and the title of the Dauphin of France, the heir to the former throne of France (the title literally meaning "The Dolphin of France").

Dolphins are present in the coat of arms of Anguilla and the coat of arms of Romania,[181] and the coat of arms of Barbados has a dolphin supporter.[182][183]

The coat of arms of the town of Poole, Dorset, England, first recorded in 1563, includes a dolphin, which was historically depicted in stylised heraldic form, but which since 1976 has been depicted naturalistically.[184]

In captivity

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SeaWorld show featuring bottlenose dolphins and pilot whales.

The renewed popularity of dolphins in the 1960s resulted in the appearance of many dolphinaria around the world, making dolphins accessible to the public. Criticism and animal welfare laws forced many to close, although hundreds still exist around the world. In the United States, the best known are the SeaWorld marine mammal parks. In the Middle East the best known are Dolphin Bay at Atlantis, The Palm[185] and the Dubai Dolphinarium.[186]

A dolphin looks at a guest at SeaWorld San Diego

Various species of dolphins are kept in captivity. These small cetaceans are more often than not kept in theme parks, such as SeaWorld, commonly known as a dolphinarium. Bottlenose dolphins are the most common species of dolphin kept in dolphinariums as they are relatively easy to train, have a long lifespan in captivity and have a friendly appearance. Hundreds if not thousands of bottlenose dolphins live in captivity across the world, though exact numbers are hard to determine. Other species kept in captivity are spotted dolphins, false killer whales and common dolphins, Commerson's dolphins, as well as rough-toothed dolphins, but all in much lower numbers than the bottlenose dolphin. There are also fewer than ten pilot whales, Amazon river dolphins, Risso's dolphins, spinner dolphins, or tucuxi in captivity.[187] An unusual and very rare hybrid dolphin, known as a wolphin, is kept at the Sea Life Park in Hawaii, which is a cross between a bottlenose dolphin and a false killer whale.[188]

The number of orcas kept in captivity is very small, especially when compared to the number of bottlenose dolphins, with 60 captive orcas being held in aquaria as of 2017.[189] The orca's intelligence, trainability, striking appearance, playfulness in captivity and sheer size have made it a popular exhibit at aquaria and aquatic theme parks. From 1976 to 1997, 55 whales were taken from the wild in Iceland, 19 from Japan, and three from Argentina. These figures exclude animals that died during capture. Live captures fell dramatically in the 1990s, and by 1999, about 40% of the 48 animals on display in the world were captive-born.[32]

Organizations such as the Mote Marine Laboratory rescue and rehabilitate sick, wounded, stranded or orphaned dolphins while others, such as the Whale and Dolphin Conservation and Hong Kong Dolphin Conservation Society, work on dolphin conservation and welfare. India has declared the dolphin as its national aquatic animal in an attempt to protect the endangered Ganges river dolphin. The Vikramshila Gangetic Dolphin Sanctuary has been created in the Ganges river for the protection of the animals.[190]

Military

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A military dolphin

A number of militaries have employed dolphins for various purposes from finding mines to rescuing lost or trapped humans. The military use of dolphins drew scrutiny during the Vietnam War, when rumors circulated that the United States Navy was training dolphins to kill Vietnamese divers.[191] The United States Navy denies that at any point dolphins were trained for combat. Dolphins are still being trained by the United States Navy for other tasks as part of the U.S. Navy Marine Mammal Program. The Russian military is believed to have closed its marine mammal program in the early 1990s. In 2000 the press reported that dolphins trained to kill by the Soviet Navy had been sold to Iran.[192]

The military is also interested in disguising underwater communications as artificial dolphin clicks.[193]

Therapy

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Dolphins are an increasingly popular choice of animal-assisted therapy for psychological problems and developmental disabilities. For example, a 2005 study found dolphins an effective treatment for mild to moderate depression.[194] This study was criticized on several grounds, including a lack of knowledge on whether dolphins are more effective than common pets.[195] Reviews of this and other published dolphin-assisted therapy (DAT) studies have found important methodological flaws and have concluded that there is no compelling scientific evidence that DAT is a legitimate therapy or that it affords more than fleeting mood improvement.[196]

Controversy

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Shamu in 2009, with a collapsed dorsal fin.

There is debate over the welfare of cetaceans in captivity, and often welfare can vary greatly dependent on the levels of care being provided at a particular facility. In the United States, facilities are regularly inspected by federal agencies to ensure that a high standard of welfare is maintained.[citation needed] Additionally, facilities can apply to become accredited by the Association of Zoos and Aquariums (AZA), which (for accreditation) requires "the highest standards of animal care and welfare in the world" to be achieved. Facilities such as SeaWorld and the Georgia Aquarium are accredited by the AZA. Organizations such as World Animal Protection and the Whale and Dolphin Conservation campaign against the practice of keeping them in captivity. In captivity, they often develop pathologies, such as the dorsal fin collapse seen in 60–90% of male orca. Captives have vastly reduced life expectancies, on average only living into their 20s, although there are examples of orcas living longer, including several over 30 years old, and two captive orcas, Corky II and Lolita, are in their mid-40s. In the wild, females who survive infancy live 46 years on average, and up to 70–80 years in rare cases. Wild males who survive infancy live 31 years on average, and up to 50–60 years.[197] Captivity usually bears little resemblance to wild habitat, and captive whales' social groups are foreign to those found in the wild. Critics claim captive life is stressful due to these factors and the requirement to perform circus tricks that are not part of wild orca behavior. Wild orcas may travel up to 160 kilometres (100 mi) in a day, and critics say the animals are too big and intelligent to be suitable for captivity.[198] Captives occasionally act aggressively towards themselves, their tankmates, or humans, which critics say is a result of stress.[199]

Although dolphins generally interact well with humans, some attacks have occurred, most of them resulting in small injuries.[200] Orcas, the largest species of dolphin, have been involved in fatal attacks on humans in captivity. The record-holder of documented orca fatal attacks is a male named Tilikum,[201][202][203] who lived at SeaWorld from 1992 until his death in 2017.[204] Tilikum has played a role in the death of three people in three different incidents (1991, 1999 and 2010).[205] Tilikum's behaviour sparked the production of the documentary Blackfish, which focuses on the consequences of keeping orcas in captivity. There are documented incidents in the wild, too, but none of them fatal.[206]

Fatal attacks from other species are less common, but there is a registered occurrence off the coast of Brazil in 1994, when a man died after being attacked by a bottlenose dolphin named Tião.[207][208] Tião had suffered harassment by human visitors, including attempts to stick ice cream sticks down his blowhole.[209] Non-fatal incidents occur more frequently, both in the wild and in captivity.

While dolphin attacks occur far less frequently than attacks by other sea animals, such as sharks, some scientists are worried about the careless programs of human-dolphin interaction. Dr. Andrew J. Read, a biologist at the Duke University Marine Laboratory who studies dolphin attacks, points out that dolphins are large and wild predators, so people should be more careful when they interact with them.[200]

Several scientists who have researched dolphin behaviour have proposed that dolphins' unusually high intelligence in comparison to other animals means that dolphins should be seen as non-human persons who should have their own specific rights and that it is morally unacceptable to keep them captive for entertainment purposes or to kill them either intentionally for consumption or unintentionally as by-catch.[210][211] Four countries – Chile, Costa Rica, Hungary, and India – have declared dolphins to be "non-human persons" and have banned the capture and import of live dolphins for entertainment.[212][213][214]

Consumption

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Cuisine

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Plate of dolphin sashimi

In some parts of the world, such as Taiji, Japan and the Faroe Islands, dolphins are traditionally considered as food, and are killed in harpoon or drive hunts.[159] Dolphin meat is consumed in a small number of countries worldwide, which include Japan[215] and Peru (where it is referred to as chancho marino, or "sea pork").[216] While Japan may be the best-known and most controversial example, only a very small minority of the population has ever sampled it.[217]

Dolphin meat is dense and such a dark shade of red as to appear black. Fat is located in a layer of blubber between the meat and the skin. When dolphin meat is eaten in Japan, it is often cut into thin strips and eaten raw as sashimi, garnished with onion and either horseradish or grated garlic, much as with sashimi of whale or horse meat (basashi). When cooked, dolphin meat is cut into bite-size cubes and then batter-fried or simmered in a miso sauce with vegetables. Cooked dolphin meat has a flavor very similar to beef liver.[218]

Health concerns

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There have been human health concerns associated with the consumption of dolphin meat in Japan after tests showed that dolphin meat contained high levels of mercury.[219] There are no known cases of mercury poisoning as a result of consuming dolphin meat, though the government continues to monitor people in areas where dolphin meat consumption is high. The Japanese government recommends that children and pregnant women avoid eating dolphin meat on a regular basis.[220]

Similar concerns exist with the consumption of dolphin meat in the Faroe Islands, where prenatal exposure to methylmercury and PCBs primarily from the consumption of pilot whale meat has resulted in neuropsychological deficits amongst children.[219]

The Faroe Islands population was exposed to methylmercury largely from contaminated pilot whale meat, which contained very high levels of about 2 mg methylmercury/kg. However, the Faroe Islands populations also eat significant numbers of fish. The study of about 900 Faroese children showed that prenatal exposure to methylmercury resulted in neuropsychological deficits at 7 years of age

See also

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References

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Further reading

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Dolphins are toothed cetaceans belonging to the family Delphinidae, which encompasses approximately 37 extant species adapted to aquatic life in oceans and select freshwater habitats worldwide. These mammals feature streamlined, spindle-shaped bodies, a single blowhole for respiration, and specialized anatomical structures such as the for focusing. Dolphins employ echolocation—emitting high-frequency clicks and interpreting returning echoes—to detect prey, navigate murky waters, and communicate, enabling precise foraging even in low-visibility conditions. They form stable social groups called pods, often numbering from a few individuals to hundreds, where cooperative hunting, alliance formation, and kin-based affiliations facilitate survival and reproduction. Empirical studies reveal dolphins possess large, convoluted brains relative to body size, supporting advanced cognitive abilities including tool use, self-recognition, and problem-solving, which rival those observed in great apes. While celebrated for their and playfulness, dolphins face anthropogenic pressures such as , degradation, and , underscoring the need for evidence-based conservation grounded in and ecological roles.

Taxonomy and Classification

Definition and Distinction from Porpoises and Whales

Dolphins are aquatic mammals belonging to the family Delphinidae in the suborder Odontoceti (toothed whales) of the order Cetacea, comprising approximately 90 extant species that vary in size from the 1.2-meter-long Maui's dolphin to the 9.5-meter orca. These species exhibit a streamlined fusiform body adapted for agile swimming, a distinct elongated rostrum or beak, conical teeth numbering up to 250 for grasping prey, and typically a falcate (curved) dorsal fin. Porpoises, by contrast, constitute the separate family Phocoenidae, also within Odontoceti, but limited to seven species, all smaller than most dolphins, with body lengths rarely exceeding 2.3 meters. Key distinctions include spade-shaped teeth rather than conical, a blunt rounded head without a pronounced , and a triangular rather than curved , reflecting adaptations for different foraging strategies and less acrobatic locomotion. While both groups are toothed cetaceans sharing echolocation and air-breathing traits, porpoises tend to be more solitary and coastal, whereas dolphins often form larger social pods in open oceans. The term "whale" broadly applies to all cetaceans but conventionally denotes larger members, including the toothless baleen whales of suborder Mysticeti, which filter-feed using keratinous baleen plates, and sizable odontocetes like the exceeding 20 meters. Dolphins and porpoises, though technically small toothed whales, are distinguished from these by their generally smaller size, predatory dentition, and absence of baleen, with the Delphinidae excluding the deeper-diving physeterids and ziphiids. This taxonomic separation underscores evolutionary divergences within Cetacea, originating from artiodactyl ancestors around 50 million years ago.

Major Families and Species Diversity

The dolphin families fall within the suborder Odontoceti of cetaceans, encompassing small- to medium-sized toothed adapted to marine and freshwater environments. These families exhibit significant morphological and ecological diversity, ranging from coastal oceanic species to strictly riverine forms, with variations in body size from under 2 meters in species like the Maui's dolphin to over 9 meters in the killer whale. The largest and most diverse family is Delphinidae, comprising 38 extant species of oceanic dolphins distributed across all major oceans. This family includes genera such as Tursiops (bottlenose dolphins), (common dolphins), Stenella (spinner and spotted dolphins), and (killer whale), reflecting adaptations for open-water foraging, social pod structures, and echolocation-dependent hunting. Delphinids dominate global dolphin biomass and sightings due to their pelagic and neritic habitats, with species like the (Tursiops truncatus) serving as ecological indicators in temperate and tropical seas. Four smaller families represent river dolphins, each typically monotypic or with limited species, confined to freshwater rivers and estuaries in , , and historically . These include:
FamilySpecies CountRepresentative Species and Notes
Iniidae1 (Inia geoffrensis), adapted to murky waters with flexible necks and enhanced electroreception.
Platanistidae2 (Platanista gangetica) and (Platanista minor), blind species relying on acoustic in silt-laden South Asian rivers.
Pontoporiidae1 (Pontoporia blainvillei), or franciscana, inhabiting coastal and estuarine South American waters with high vulnerability.
Lipotidae1 (Lipotes vexillifer), the River dolphin, declared functionally extinct by 2006 surveys showing no viable population, though listed as pending confirmation.
This distribution yields a total of approximately 43 dolphin species, underscoring the family's evolutionary success in diverse aquatic niches despite varying conservation threats like habitat fragmentation for riverine forms.

Evolutionary History

Origins from Terrestrial Ancestors

Dolphins, as members of the odontocete suborder of cetaceans, share a common evolutionary origin with other whales from terrestrial artiodactyls, specifically within the even-toed ungulates (Artiodactyla). Molecular phylogenetic analyses, including comparisons of milk casein genes and phylogenomic data, indicate that cetaceans form a monophyletic clade with hippopotamuses (Hippopotamidae), diverging from other artiodactyls approximately 59 million years ago during the Paleocene-Eocene transition. This "Whippomorpha" grouping is supported by shared retrotransposon insertions (SINEs) and ankle bone morphology, such as the double-pulley astragalus, which distinguishes artiodactyls from other mammals. The basal cetacean lineage traces back to small, terrestrial or semi-terrestrial resembling raoellids, such as from the late Eocene of and , dated to around 48-47 million years ago. These ancestors were goat-sized herbivores or omnivores that inhabited forested, riverine environments, with dense limb bones suggesting wading or diving behaviors for predator evasion or foraging, evidenced by isotopic analysis of indicating a diet mixing terrestrial plants and aquatic prey. Raoellids represent the closest non-cetacean relatives, bridging the gap from fully terrestrial like Elomeryx to early cetaceans through gradual adaptations in auditory structures and limb proportions. The first unambiguous cetaceans emerged in the early Eocene, exemplified by , known from fossils in dated to 53.5-49 million years ago. This wolf-sized predator possessed fully terrestrial quadrupedal locomotion with hooves on its toes, a long snout suited for terrestrial hunting, and ears adapted for underwater hearing, though it likely foraged near freshwater systems for and small vertebrates rather than being fully aquatic. Cladistic studies of skeletons confirm its placement as the sister taxon to all later cetaceans, nested within Artiodactyla rather than with extinct mesonychians, based on shared dental and cranial features like double-rooted cheek teeth. This transition reflects a selective pressure for amphibious lifestyles in Eocene coastal ecosystems, setting the stage for full marine colonization.

Aquatic Adaptations and Fossil Record

The fossil record of cetaceans, the order encompassing dolphins, reveals a transition from terrestrial artiodactyl ancestors to fully aquatic forms spanning roughly 50 million years, beginning in the early Eocene epoch. Earliest fossils, such as Pakicetus from approximately 49 million years ago in present-day Pakistan, exhibit semi-aquatic traits including dense limb bones for diving stability and auditory adaptations for underwater hearing, while retaining terrestrial locomotion capabilities. Subsequent forms like Ambulocetus (circa 48 million years ago), an amphibious "walking whale" with webbed feet and a crocodile-like body, demonstrate progressive reliance on aquatic propulsion through pelvic rotation and tail undulation. By the late Eocene and , archaeocetes such as (around 40-34 million years ago) show advanced adaptations including reduced hind limbs, elongated bodies, and the emergence of a dorsal blowhole precursor, marking near-complete commitment to marine life with vestigial pelvises no longer supporting weight. Odontocetes, the suborder including modern dolphins (Delphinidae family), first appear in the fossil record during the Oligocene-Miocene transition about 34-23 million years ago, with early forms like Xenorophus displaying toothed jaws and echolocation-enabling skull asymmetry. True delphinids, resembling contemporary dolphins, proliferated in the Miocene around 15-12 million years ago, coinciding with and ocean restructuring that favored agile, predatory niches. Aquatic adaptations in dolphins, evidenced through comparative anatomy of fossils and extant species, center on hydrodynamic efficiency and sensory specialization. The fusiform body plan minimizes drag, with flexible vertebrae enabling rapid maneuvers up to 55 km/h in bursts for species like the bottlenose dolphin (Tursiops truncatus). Forelimbs evolved into pectoral flippers with hyperphalangy—excess finger bones—for steering, while hind limbs atrophied entirely, freeing pelvic girdles for internal support. The tail fluke, absent in early cetaceans but developed by the Miocene, provides thrust via vertical oscillation, contrasting fish-like lateral movement and reflecting mammalian spinal constraints. Respiratory and integumentary shifts further underscore : the migrated posteriorly to form a blowhole for surfacing breaths, reducing submersion time risks, while layers replaced for insulation and , as inferred from Eocene fossils showing initial fat deposition. Genomic studies corroborate these morphological changes, identifying losses in genes for terrestrial traits like olfaction and production, facilitating full-time aquatic existence without reversing to land. Fossils confirm no reversals in this trajectory, with delphinid diversification aligning with ecological pressures for speed and in open oceans.

Anatomy and Physiology

Body Structure and Locomotion

Dolphins exhibit a body plan, tapered at both ends with a maximal girth near the midsection, which reduces drag during swimming compared to other shapes. This hydrodynamic form consists of a blunt head housing the and rostrum, a cylindrical trunk, and a narrowed tail stock leading to horizontal flukes. Body sizes vary widely across the approximately 90 species in the suborder Odontoceti; the Maui's dolphin (Cephalorhynchus hectori maui) reaches only 1.7 meters in length and 50 kilograms, while the (Orcinus orca) grows to 9.5 meters and 10 tonnes. A representative species, the (Tursiops truncatus), typically measures 2 to 4 meters long and weighs 150 to 650 kilograms in adulthood. The supports this form with adaptations for aquatic efficiency, including a flexible axial column of up to 60 vertebrae enabling lateral undulation and a reduced number of fused to the for streamlined contour. Forelimbs have evolved into pectoral flippers with a featuring a , , , and hyperphalangic digits encased in for maneuverability, while elements are vestigial and internalized. The , variably falcate or triangular depending on , provides stability against roll, and lacks skeletal support, being composed of fibrous . Locomotion relies on thrust generated by vertical oscillations of the tail flukes, powered by antagonistic epaxial and hypaxial musculature along the vertebral column, rather than limb-based paddling. This thunniform swimming yields stride lengths of approximately 0.9 body lengths per tailbeat at low speeds, with peak velocities reaching 37 miles per hour (60 km/h) in species like the common dolphin (Delphinus delphis) for short bursts. Pectoral fins and body flexion contribute to steering and turning, allowing agile maneuvers essential for foraging and evasion. Dolphins also employ behaviors like porpoising—leaping clear of the surface—to minimize drag and conserve oxygen during sustained travel.

Integumentary and Respiratory Systems

The integument of dolphins comprises a multilayered structure adapted for aquatic life, including a thick , , and underlying hypodermis of . Lacking or scales, the skin features microscopic ridges that contribute to drag reduction during swimming. The epidermis exhibits rapid cell turnover, with the outermost layer in bottlenose dolphins (Tursiops truncatus) replaced every two hours—nine times faster than in humans—to maintain a smooth, hydrodynamic surface and facilitate shedding of parasites and debris. Blubber, the lipid-rich hypodermis, serves multiple functions: , regulation, and . In bottlenose dolphins, thickness can more than double from neonatal to adult stages, varying with nutritional status; emaciated adults show reductions up to 26% compared to healthy counterparts. Specialized structures like Merkel cells in the act as mechanoreceptors, aiding tactile sensitivity despite the streamlined exterior. Dolphins possess a centered on paired lungs accessed via a single dorsal blowhole, an evolutionary modification of the positioned for efficient surfacing. The blowhole is sealed by a muscular flap that prevents entry during submersion, opening only briefly for . Upon surfacing, dolphins exhale forcefully before inhaling, completing the breath cycle in about 0.3 seconds to minimize exposure time. Adaptations for prolonged apnea include the dive response—bradycardia, peripheral , and blood flow redistribution—along with elevated in muscles for . Bottlenose dolphins typically dive for 20-40 seconds, with maximum voluntary apneas reaching 255 seconds and exceptional records up to 15 minutes, supported by lung capacities that allow efficient oxygen management without full collapse during descent. Surface breathing rates average 2.2-2.3 breaths per minute in bottlenose dolphins.

Sensory Organs and Perception

Dolphins, as odontocete cetaceans, possess highly specialized sensory systems adapted for an aquatic environment, with audition and echolocation serving as the dominant modalities for perception, navigation, and foraging. Echolocation involves the production of high-frequency clicks generated through phonic lips in the nasal passages, which are focused and directed forward by the fatty in the . These clicks typically range from 40 to 150 kHz in bottlenose dolphins (Tursiops truncatus), enabling fine ; for instance, the system can distinguish targets separated by as little as 1-2 cm at short ranges due to the short of the signals. Auditory sensitivity extends from approximately 75 Hz to 150 kHz, with peak sensitivity between 10 and 80 kHz, far surpassing hearing capabilities and allowing detection of prey echoes even in turbid waters where vision fails. The lower and tissues conduct returning echoes to the middle and inner ears, which feature enlarged auditory bullae and thick fibers—two to three times the diameter of those in terrestrial mammals—for rapid . Vision in dolphins is functional but secondary to echolocation, with eyes positioned laterally and adapted for both aerial and underwater viewing through a double-slit that adjusts to varying levels. Acuity is comparable in air and , estimated at about 6/60 to 6/120 in equivalents, sufficient for detecting movement or conspecifics at distances up to several meters in clear conditions but limited by the lack of a reflective and sensitivity to low . Empirical tests show dolphins can discriminate shapes and colors underwater, though performance degrades in murky or deep environments, underscoring reliance on acoustic cues. Olfaction is vestigial or absent, as evidenced by the degeneration of olfactory bulbs and nerves in most delphinids, rendering ineffective in water; this aligns with the dilution of odorants in marine habitats and the primacy of other senses. number around 1,500-2,000, allowing detection of basic qualities like sweet, bitter, sour, and salty, with behavioral preferences for certain indicating gustatory discrimination during feeding. Tactile sensitivity is acute via the skin, particularly around the rostrum and fins, facilitating social interactions and object exploration, while recent studies confirm passive electroreception through specialized pits on the snout, detecting DC fields as weak as 2.4-5.5 μV/cm to locate bioelectric signatures of hidden prey. These multimodal senses integrate for comprehensive environmental awareness, though may impair full expression due to spatial constraints on acoustic ranging.

Cognitive Abilities

Empirical Tests of Intelligence

Bottlenose dolphins (Tursiops truncatus) have demonstrated self-recognition in mirror tests, a benchmark for assessing self-awareness in non-human animals. In a 2001 study, two dolphins were marked on their bodies and exposed to mirrors; they used the reflections to investigate the marks on inaccessible areas, such as their heads, while ignoring sham marks, indicating contingency behaviors consistent with self-directed inspection rather than social responses. Similar results were replicated in subsequent experiments, with dolphins orienting toward mirror images to view marked regions, supporting cognitive convergence toward self-recognition capabilities observed in great apes and humans. Precocious development of this trait has been observed, with some dolphins exhibiting mirror-guided self-inspection as early as 4-7 weeks of age, earlier than in human children or other tested species. Empirical assessments of linguistic comprehension reveal dolphins' ability to process syntactic and semantic structures. Research by Louis Herman and colleagues from 1979 to the 1980s trained bottlenose dolphins to comprehend imperative sentences in gestural or acoustic artificial s, achieving over 80% accuracy in executing novel commands involving object manipulation, such as "tandem-hoop-frisbee," which required cooperative actions with specific referents. Dolphins distinguished between semantic roles (e.g., actor-object vs. object-actor) and syntactic embeddings, generalizing rules to untrained sentences, though performance declined with increasing complexity, suggesting limits in recursive processing akin to human boundaries. Referential gestures were also understood, with dolphins selecting indicated objects in arrays, interpreting human-directed points as symbolic cues rather than attentional signals. Problem-solving tasks highlight and . In cooperative pulling experiments, bottlenose dolphins learned to synchronize actions with partners to retrieve rewards from a submerged , inhibiting individual responses until the partner was in position, demonstrating comprehension and timing adjustment over 20-50 trials. Dolphins solved novel apparatus-based challenges by planning sequences, such as displacing weights to access platforms, adapting behaviors across sessions without explicit for planning per se. Vocal coordination during tandem tasks, including signature whistles, facilitated joint problem-solving, with acoustic exchanges preceding successful outcomes in puzzles requiring synchronized pulls. Memory capacities exceed those of many mammals in duration and specificity. Bottlenose dolphins retain recognition of conspecific whistles after separations of up to 20 years, responding selectively to familiar signatures in playback tests, independent of relatedness or length, indicating lifelong social . Episodic-like was evidenced in incidental encoding tasks, where dolphins recalled unreinforced event details (e.g., object locations and actions) after delays of hours, matching what-where-when criteria without cueing, comparable to avian and analogs. These findings derive from controlled captive studies, though is debated due to enriched training environments potentially inflating performance relative to wild conditions.

Tool Use and Problem-Solving Evidence

One prominent example of tool use among dolphins occurs in a subpopulation of bottlenose dolphins (Tursiops aduncus) in , , where individuals, predominantly females, employ marine sponges as protective tools to shield their rostrums while for prey on the seafloor. This behavior, first documented in the , involves selecting and carrying basket sponges (Ircinia sp.) over distances of up to 20 kilometers, with tool users spending approximately 20% more time on the seafloor than non-users, indicating a specialization in prey-scarce habitats. Genetic analyses confirm that sponge use is not driven by ecological or kinship factors alone but by cultural transmission, often maternally, as calves learn the technique through observation rather than innate predisposition. Social network studies further reveal that "spongers" form distinct clusters, with tool use persisting across generations despite its energetic costs, such as reduced efficiency. Empirical evidence for problem-solving in dolphins derives from controlled experiments demonstrating flexible . In apparatus-based tasks, bottlenose dolphins (Tursiops truncatus) have exhibited by manipulating weighted objects to access rewards, adjusting behaviors based on trial-and-error feedback over sessions. paradigms for , where dolphins generate responses to stimuli, show that they can produce creative sequences, such as combining vocalizations with gestures, interpretable as indicators of abstract problem-solving rather than . Captive studies at facilities like the Dolphin Research Center have documented with adaptive flexibility, where dolphins solve puzzles by mirroring or conspecific actions in inverted or delayed contexts, outperforming simple repetition. One dolphin in cognitive enrichment trials repeatedly solved mechanical puzzles without consuming rewards, persisting for the intrinsic challenge, suggesting motivation beyond immediate reinforcement. These findings, drawn from longitudinal field observations and replicable lab protocols, underscore dolphins' capacity for in tool modification and sequential problem-solving, though limited to opportunistic rather than manufactured tools in . Peer-reviewed sources like PNAS and provide robust, multi-method validation, mitigating confounds from anecdotal reports.

Comparative Assessments and Limitations

Dolphins possess relatively large brains for their body size, with bottlenose dolphins exhibiting an (EQ) of approximately 4.14, higher than that of chimpanzees (2.2–2.5) and (1.67–1.87), but lower than humans (7.4–7.8). This metric, which adjusts relative to expected for a given body , suggests advanced cognitive potential, though dolphin brains feature a less developed compared to , limiting like planning. Empirical tests, such as mirror self-recognition (MSR), indicate in bottlenose dolphins, where individuals marked with visible ink directed attention to the mark via mirrors, a capability shared with humans, great apes, and but absent in most other animals. Dolphins demonstrate MSR as early as 7 months of age, preceding the typical onset in human infants (12–18 months) and comparable to or earlier than in chimpanzees. In problem-solving paradigms, dolphins perform on par with great apes and corvids in associative learning and cooperative tasks, such as using acoustic signals to coordinate foraging, but show limitations in tasks requiring sustained tool use or abstract symbolism due to their lack of manipulative appendages. Vocal mimicry and signature whistles enable individual recognition akin to primate calls, yet dolphins do not exhibit cumulative cultural transmission observed in humans or evidence of syntactic language structure. Comparative rankings place dolphins among the top non-human intelligences, often alongside chimpanzees and elephants, based on social complexity and adaptability, though corvids may surpass them in causal reasoning puzzles adapted for beak manipulation. Assessments of dolphin cognition face inherent limitations from anthropocentric biases in experimental design, which prioritize visual and terrestrial manipulative skills ill-suited to aquatic, echolocating species. For instance, mirror tests assume visual self-perception, potentially underestimating echolocation-based awareness, while the absence of opposable digits precludes direct comparisons in tool fabrication to primates. Interspecies differences in sensory modalities—dolphins' reliance on over vision—and ecological contexts hinder equitable evaluation, as behaviors like formation may reflect domain-specific adaptations rather than general . Longitudinal field studies are scarce due to underwater observation challenges, leading to overreliance on captive data that may not capture wild cognitive demands, and no validated metric exists for cross-species abstraction or without human-like outputs.

Behavior

Social Structures and Group Dynamics

Bottlenose dolphins (Tursiops truncatus) exhibit fission-fusion social structures, in which group composition dynamically changes as individuals join or leave over timescales from minutes to hours. This fluidity, observed in populations such as those in , , enables adaptive responses to ecological pressures like resource availability and predation risks. Empirical studies document average subgroup sizes ranging from 2 to 10 individuals within larger communities of hundreds, with aggregations occasionally exceeding 100 during favorable conditions. Female bottlenose dolphins display matrilineal , maintaining long-term associations with maternal kin and remaining in natal home ranges. Genetic analyses from long-term field observations confirm that daughters inherit and sustain their mothers' social networks, fostering stable bonds that persist for decades and correlate with benefits. Mothers with calves often form core units, prioritizing kin-biased affiliations that enhance calf survival through and vigilance. In contrast, male dolphins form multilevel cooperative to compete for access, with first-order pairs or trios receptive females. Second- and third-order , comprising up to 14 unrelated males, coordinate in intergroup conflicts, as evidenced by 30-year longitudinal data from showing strategic partner selection based on cooperative history. Paternity assignments via genetic sampling reveal that males in larger sire more offspring, underscoring the adaptive value of these coalitions in a promiscuous . Juvenile males engage in play that rehearses alliance behaviors, predicting adult . Across delphinid species, social dynamics vary, but fission-fusion predominates in oceanic dolphins, contrasting with more stable pods in some coastal forms; however, bottlenose patterns exemplify the complexity, with alliances rivaling coalitions in scale and sophistication.

Reproduction, Mating, and Hybridization

Dolphins are viviparous mammals that typically give birth to a single calf after a period of approximately 12 months, as observed in bottlenose dolphins (Tursiops truncatus). Calving intervals vary by species but often span 2–4 years, influenced by duration and environmental factors; for common dolphins (Delphinus delphis), intervals average 3.15 years when accounting for , , and resting phases. Females reach between 8–10 years, with first around 9–10 years in some populations. Births occur tail-first to facilitate underwater delivery, and calves are precocial, able to swim immediately but dependent on maternal milk for 1–2 years. Mating in dolphins is characterized by a promiscuous system, where both sexes engage with multiple partners, promoting evidenced by large testes relative to body size and moderate in males. Males often form alliances or "bromances" to herd receptive females, isolating them from rivals and facilitating coerced s, as documented in pods. involves synchronized swimming, aerial displays, and vocalizations, with little evidence of pair-bonding or post-conception; can occur during , enabling rapid rebreeding. Many lack strict , though peaks align with resource abundance, such as spring leading to spring births in coastal bottlenose populations. Interspecies hybridization, though rare in the wild due to ecological and behavioral barriers, has been documented both in and , yielding fertile offspring in some cases. Notable examples include the , a hybrid of female and male (Pseudorca crassidens), which has reproduced in . Wild hybrids include a (Peponocephala electra) crossed with a (Steno bredanensis) observed off in 2018, displaying intermediate morphology like a bottle-shaped head and small . Captive intra-generic hybrids between common (T. truncatus) and Indo-Pacific bottlenose dolphins (T. aduncus) confirm genetic viability, with molecular analyses revealing mixed ancestry. Such events underscore sympatric species' potential for but are limited by and divergence, with no widespread hybrid populations identified.

Foraging Strategies and Diet

Dolphins, members of the family Delphinidae, maintain carnivorous diets dominated by and cephalopods, with occasional crustaceans comprising a minor portion. Prey selection reflects and species-specific adaptations; for example, coastal bottlenose dolphins (Tursiops truncatus) consume such as mullet and alongside , yielding diets with at least 21 fish families and 31 species documented in southeastern U.S. populations. Oceanic species like short-beaked common dolphins (Delphinus delphis) emphasize and cephalopods, with seasonal shifts favoring abundant schools; cephalopods constitute up to 20-30% by mass in some analyses. Hector's dolphins (Cephalorhynchus hectori) target benthic and midwater prey across water columns, underscoring opportunistic feeding tied to local prey availability rather than fixed preferences. Foraging strategies leverage echolocation for precise prey localization, combined with hydrodynamic agility to pursue schools at speeds exceeding 20 km/h. Solitary tactics predominate in low-prey-density environments, but group coordination enhances efficiency in schooling fish; spinner dolphins (Stenella longirostris) form synchronized formations of 16-28 individuals to compress prey balls, increasing density by up to 200-fold during nocturnal hunts. Bottlenose dolphins exhibit culturally transmitted behaviors, with 94.5% of documented tactics in this and killer whale (Orcinus orca) populations involving social learning from mothers or peers, as evidenced by developmental observations in wild groups. Specialized tactics include strand feeding by southeastern U.S. bottlenose dolphins, where coordinated groups toward shallow sandbars, generating waves to strand schools onshore before beaching themselves to capture prey—a risky, learned absent in non-local populations and transmitted vertically within matrilines. Barrier and shipside feeding exploit environmental features like reefs or vessel wakes to trap prey, demonstrating plasticity influenced by prey type and . with humans, observed in Brazilian lagoons since at least the 1840s, yields mutual benefits through synchronized dives but declines with disruptions, highlighting dependence on stable prey dynamics. These strategies prioritize energy efficiency, with group reducing individual search costs by 13-20% in modeled scenarios, though success varies by prey escape responses and environmental predictability.

Communication and Vocalizations

Dolphins employ a repertoire of acoustic signals broadly classified into three categories: frequency-modulated whistles, clicks, and burst-pulse sounds. Whistles, typically with harmonics, facilitate long-distance social communication, conveying information about identity, location, or group coordination. Clicks, produced as short, high-frequency pulses, primarily enable echolocation for and , while burst-pulse sounds, consisting of rapid click trains, are associated with close-range interactions, including or play. These vocalizations are generated via air movement through specialized nasal passages and phonic lips, with sounds modulated by muscular control and amplified through the dolphin's —a fatty structure in the forehead that focuses outgoing signals. Signature whistles represent a key feature of dolphin vocal individuality, where each dolphin develops a unique contour early in life, which persists and serves to identify the caller, akin to a personal identifier rather than a with semantic content. Long-term observations of bottlenose dolphins (Tursiops truncatus) in Sarasota Bay, , spanning over 30 years, reveal that calves acquire signature whistles from mothers within the first weeks of life and that dolphins can mimic these whistles to address specific individuals, aiding reunion in dispersed groups. Experimental playbacks confirm that dolphins respond preferentially to their own signature whistles, ignoring others, indicating learned recognition and potential use in social bonding or recruitment. However, while such specificity suggests referential signaling, claims of full linguistic equivalence overstate the evidence, as dolphin whistles lack demonstrated syntax or arbitrary symbols combining to form novel meanings. Echolocation relies on clicks emitted at rates up to 1,000 per second during , with frequencies ranging from 20 to 120 kHz, allowing dolphins to resolve objects as small as 1 cm at distances exceeding 100 meters in clear water. The mechanism involves rapid air compression in nasal bursae, producing clicks that propagate through the for beam-forming and reflect off targets, returning echoes received by the lower jaw and transmitted to the via fat-filled channels. This system provides detailed acoustic images of shape, size, and texture, enabling prey detection in murky conditions where vision fails; for instance, dolphins adjust click intensity and inter-click intervals based on target range, shortening intervals as they close in. Adaptive beam width, narrower for precision tasks, underscores the efficiency of this active , honed by evolutionary pressures for aquatic hunting. Burst-pulse sounds, overlapping in function with whistles and clicks, feature click trains at rates exceeding 600 per second, producing low-frequency components audible over short ranges for agonistic displays or prey. These nonlinear phenomena, including jumps and sidebands, may enhance signal salience in noisy environments or convey emotional states, though empirical decoding remains elusive. Studies indicate burst pulses correlate with physical proximity and intensity of interactions, such as during chases, but do not exhibit consistent contextual rules akin to . Overall, while dolphin vocalizations demonstrate contextual flexibility and individual specificity, supporting complex social coordination, no verified evidence supports generative or referential language; sequences appear associative rather than rule-bound, limited by the medium's constraints and .

Aggressive Behaviors and Infanticide

Dolphins exhibit a spectrum of aggressive behaviors, including with the rostrum, , tail-slapping, and chasing, observed across in both wild and captive settings. These actions occur in contexts such as male-male for access to females, defense of resources, and establishment of dominance within pods. In bottlenose dolphins (Tursiops truncatus), aggressive interactions often involve physical contact that can result in injuries like rake marks from teeth or from impacts. In bottlenose dolphins, video analyses from 1997 to 2007 documented frequent aggressive episodes, with males directing toward both conspecifics and females during consortships. Intraspecific aggression frequently escalates during reproductive seasons, where coalitions of adult males isolate and coerce females into , employing tactics like and physical that can cause exhaustion or to the targeted or her offspring. Such behaviors reflect underlying , where males prioritize reproductive opportunities over or calf welfare. Interspecific aggression is also prevalent, particularly among s targeting smaller cetaceans. In Scottish coastal waters, postmortem examinations of stranded harbor porpoises (Phocoena phocoena) revealed that a bore injuries—such as fractured ribs, deep lacerations, and internal hemorrhaging—consistent with deliberate attacks by bottlenose dolphins, rather than predation for sustenance. Similar patterns appear in attacks on striped dolphins (Stenella coeruleoalba), where 14 cases in the Mediterranean showed trauma indicative of bottlenose dolphin as the primary mortality cause, including spinal fractures and damage from ramming and biting. These interactions, often involving multiple dolphins ganging up on a single victim, suggest motivations like redirected intraspecific or behavioral conditioning rather than caloric gain, as victims are typically not consumed. Infanticide, the killing of dependent calves by unrelated adult males, has been empirically documented in multiple bottlenose dolphin populations and aligns with evolutionary pressures to accelerate female reproductive cycles. In , , long-term observations identified male s systematically targeting and drowning calves, with post-killing mating attempts on the bereaved mothers occurring shortly thereafter, thereby shortening interbirth intervals. Necropsy data from the Western North Atlantic corroborated this, with nine calves exhibiting perimortem trauma—such as crushed skulls and rib fractures—attributable to conspecific aggression, excluding alternative causes like predation. In Pacific white-sided dolphins (Lagenorhynchus obliquidens), a 75-minute by 10 individuals (predominantly males) on a neonate resulted in visible gashes and presumed lethality, interpreted as an attempt. This behavior, observed sporadically but recurrently, enhances male fitness by eliminating competitors' offspring and inducing cessation in females, though success rates vary by and stability. While rates are low overall—estimated at under 10% of calf mortality in studied groups—its persistence underscores dolphins' capacity for calculated driven by reproductive imperatives, challenging anthropocentric views of cetacean benevolence.

Ecology

Habitats, Migration, and Distribution

Dolphins occupy a broad spectrum of aquatic habitats worldwide, spanning marine, estuarine, and freshwater environments depending on the . The majority belong to the oceanic family Delphinidae, which inhabits temperate and tropical waters across all major oceans, including coastal shelves, bays, gulfs, open pelagic zones, and deeper offshore areas where surface temperatures typically range from 10°C to 32°C. These species favor environments with abundant prey, such as schools and , and often congregate near zones or continental margins that enhance productivity. Distribution patterns vary by species and reflect ecological adaptations; for example, the (Tursiops truncatus) ranges widely in the Atlantic from to and in the eastern Atlantic from to , while also appearing off the U.S. West Coast, , and . The short-beaked common dolphin (Delphinus delphis) predominates in tropical and temperate waters of the Atlantic, Pacific, and Indian Oceans, often in pelagic s away from shore. In contrast, freshwater dolphins—such as the (Inia geoffrensis) in the Amazon and Orinoco basins of , the (Platanista gangetica) in the Indian subcontinent's rivers, and the (Platanista gangetica minor) confined to Pakistan's —are adapted to shallow, turbid riverine systems with strong currents, excluding them from marine realms. Migration in dolphins differs markedly from that of large baleen whales, with most exhibiting resident or nomadic behaviors rather than predictable long-distance annual treks. Many populations, including coastal bottlenose dolphins, demonstrate strong site fidelity to specific bays or estuaries, moving locally in response to prey distribution or seasonal shifts. Pelagic like common dolphins may undertake broader movements following migratory prey aggregations, such as sardine runs, leading to seasonal range expansions or contractions influenced by oceanographic features like currents and upwellings. Freshwater remain largely within fixed riverine ranges, with limited upstream-downstream displacements tied to flood cycles or needs, though restricts such mobility. Overall, dolphin movements prioritize efficiency over latitudinal migration, resulting in dynamic but often localized distribution shifts.

Predator-Prey Relationships

Dolphins occupy mid- to upper-trophic levels in marine food webs, functioning primarily as predators that target schooling , cephalopods, and benthic invertebrates through echolocation-guided pursuits and cooperative herding tactics. Bottlenose dolphins (Tursiops truncatus), for instance, consume species such as mullet, eels, flounders, jacks, and , with daily intake averaging 4-6% of body weight, or up to 15-30 kg for adults. These foraging strategies exploit prey aggregations, as seen in mud-ring feeding where dolphins trap in shallow waters by creating barriers, a documented in coastal populations since observations in the 1980s. Prey availability directly influences dolphin energy budgets and reproductive success, with studies in estuarine systems showing correlations between declines and reduced calf survival rates. Despite their predatory prowess, dolphins remain vulnerable to larger apex predators, including orcas (Orcinus orca) and select species, which impose selective pressures shaping dolphin morphology, , and grouping patterns. Orcas employ pack-hunting tactics to separate calves or isolated individuals from pods, with documented attacks on bottlenose dolphins involving , drowning, and dismemberment, as observed in coastal waters off and the U.S. Southeast since the 1990s. Shark predation, primarily by tiger sharks (Galeocerdo cuvier), dusky sharks (Carcharhinus obscurus), bull sharks (Carcharhinus leucas), and great whites (Carcharhinus carcharias), targets juveniles or weakened adults, often inflicting rake marks or fatal bites; necropsies of stranded dolphins reveal shark bite frequencies up to 20% in some populations. These encounters drive anti-predator behaviors, such as "mobbing" attacks where dolphins ram predators with or flanks, leveraging speed (up to 35 km/h bursts) and group cohesion to deter assaults, thereby reducing individual mortality risks by 50-70% in larger pods. Predator-prey dynamics exhibit spatial and temporal variability, with dolphins adjusting ranging patterns to avoid high-risk zones like shark nurseries or territories, while prey schools trigger dolphin convergence via acoustic signaling. In oceanic realms, common dolphins (Delphinus delphis) face elevated predation from large during migrations, correlating with strandings peaked in summer months across the North Atlantic. Conversely, dolphins' selective can deplete local prey stocks, altering community structures; for example, intense predation on by short-beaked common dolphins influences mesopelagic distributions over scales of kilometers to basins. Such interactions underscore dolphins' role in trophic cascades, where their suppression of herbivorous indirectly affects algal blooms and health.

Population Dynamics and Natural Mortality

Dolphin populations exhibit dynamics shaped primarily by adult survival rates, which exert greater influence on growth than reproductive output in long-lived like those in Delphinidae, due to low and extended lifespans. Annual rates (λ) for unimpacted (Tursiops truncatus) populations are estimated at approximately 1.014, reflecting a balance where birth rates offset natural mortality under ideal conditions. rates among adult females vary by population; for example, in the Black Sea bottlenose dolphin subpopulation, estimates range from 290 to 407 births per 1,000 females annually, with interbirth intervals typically 2–6 years and reached between 5–13 years. These parameters contribute to intrinsic rates of increase (r) near zero in stable habitats, with sensitivity analyses indicating that perturbations in adult female survival can shift populations toward decline more rapidly than fluctuations in calf production. Natural mortality in dolphins arises from predation, infectious diseases, , and nutritional deficits, with rates varying by age class and . For bottlenose dolphins in the , overall annual mortality approximates 9.8%, with higher rates among calves (up to 20–30% in first year) due to vulnerability to predation and maternal abandonment. Predators such as large s (Carcharodon carcharias, Carcharhinus leucas) and killer whales (Orcinus orca) account for significant calf and juvenile losses, particularly in coastal habitats where dolphins overlap with predator ranges. Infectious agents, including cetacean and Brucella spp., drive episodic die-offs, as evidenced by unusual mortality events where pathology reveals and as proximate causes. In common dolphins (Delphinus delphis), mortality-at-age models suggest total natural mortality (Z) of around 0.25 annually, with at birth near 3.5 years under baseline conditions, though these estimates may underestimate early-age losses due to incomplete stranding recovery. contributes substantially during prey shortages, comprising 17% of examined mortalities in affected bottlenose populations, escalating to 61% during environmental anomalies like cold snaps that disrupt . Parasitic burdens, such as infestations leading to gastric ulceration, further elevate mortality in density-dependent scenarios, though empirical data from long-term photo-identification studies in sites like indicate adult annual survival of 0.928–0.968, implying mortality of 3.2–7.2%. Population-level trends reflect these dynamics, with viability declining in regions like the for common dolphins amid cumulative natural pressures.

Threats

Natural Predators and Diseases

Large shark species, including great white sharks (Carcharodon carcharias) and tiger sharks (Galeocerdo cuvier), prey on dolphins, targeting calves, juveniles, and occasionally adults, with evidence from healed bite scars on live individuals and remains in stomachs. In a study of Indian Ocean bottlenose dolphins (Tursiops aduncus), 10.3% of captured individuals exhibited scars or wounds consistent with bites, though only 1.2% of over 6,000 examined contained cetacean remains, indicating opportunistic rather than specialized predation. Similar bite incidence rates, around 10-15%, have been documented in Australian snubfin dolphins (Orcaella heinsohni), suggesting comparable predation pressure across coastal species. Killer whales (Orcinus orca), the largest members of the dolphin family, actively hunt smaller delphinids as part of their mammalian prey diet, using coordinated group tactics to separate and exhaust targets. Off Kaikoura, , dusky dolphins (Lagenorhynchus obscurus) experience up to a 38% reduction in foraging time due to killer whale predation risk, altering their spatial and temporal behaviors to avoid encounters. Transient killer whale pods specialize in marine mammal predation, including dolphins, with documented attacks contributing to natural mortality in populations like common bottlenose dolphins (Tursiops truncatus). Wild dolphins suffer from infectious , including viral, bacterial, fungal, and parasitic pathogens, which can cause mass mortality events and chronic conditions exacerbated by environmental stressors. Cetacean morbillivirus (CeMV), a paramyxovirus related to , triggers epizootics with high fatality rates, manifesting in , , and skin lesions; outbreaks have killed thousands of dolphins in the Atlantic since the 1980s and 2013, with lesions and neurological symptoms confirming . Fungal infections like lobomycosis (lacaziosis), caused by the unculturable fungus Lacazia loboi, produce chronic, disfiguring skin nodules in tropical and subtropical waters, primarily affecting inshore bottlenose dolphins; prevalence reaches 10-20% in some Brazilian and Amazonian populations, with lesions progressing over years and increasing susceptibility to secondary infections. Other notable pathogens include dolphin herpesviruses and papillomaviruses causing cutaneous tumors, and bacterial agents like Chlamydiaceae, detected in stranded individuals alongside CeMV. Mycotic diseases overall are widespread in marine mammals, with captive individuals showing higher susceptibility due to stress and confinement.

Anthropogenic Impacts Including Bycatch and Pollution

Bycatch, the incidental capture of non-target species in fishing gear, represents a primary anthropogenic threat to dolphin populations worldwide, with dolphins comprising a significant portion of affected cetaceans. Globally, an estimated 300,000 cetaceans, including dolphins, are killed annually through in various fishing operations such as gillnets, purse seines, and trawls. In the eastern tropical Pacific purse seine fishery, targeted conservation measures under the U.S. achieved a greater than 99% reduction in dolphin from peak levels in the 1960s-1980s, dropping annual spotted dolphin deaths from over 400,000 to fewer than 1,000 by the early 2020s. However, common dolphins (Delphinus delphis) remain highly vulnerable in regions like the and North Atlantic, where rates can reach 1-2% of local populations annually, exacerbating declines in small cetacean stocks. In European waters, a 2017 mass stranding event of over 200 common dolphins along the French Atlantic coast revealed that 85% of necropsied individuals bore injuries consistent with fishing gear interactions, such as net marks and hook damage. Pollution from chemical contaminants and plastics further compounds dolphin mortality and sublethal effects, impairing reproduction, immune function, and foraging efficiency. Persistent organic pollutants (POPs) like polychlorinated biphenyls (PCBs) accumulate in dolphin blubber via in prey, with elevated PCB levels in UK-stranded common dolphins correlating with increased infectious disease risk, including and skin lesions, based on analysis of 836 specimens from 1990-2020. Oil spills introduce acute toxins; for instance, the 2010 spill exposed bottlenose dolphins (Tursiops truncatus) in the to polycyclic aromatic hydrocarbons, leading to documented disease, , and higher calf mortality rates in affected pods through 2020. Plastic debris poses direct ingestion risks, causing intestinal blockages, , and internal injuries; necropsies of stranded dolphins frequently reveal macroplastics in stomachs, while embed in and fat tissues, as found in two-thirds of examined marine mammals from U.S. coastal strandings in a 2023 study. Recent findings indicate dolphins exhale via blowholes, with bottlenose dolphins inhaling higher doses due to deep capacities—up to 10 times human exposure rates in polluted coastal zones—potentially exacerbating respiratory and systemic toxicity. These impacts interact synergistically; for example, weakened dolphins from pollutant exposure become more susceptible to entanglement, while gear-embedded plastics introduce secondary chemical leaching. Coastal and riverine dolphin species, such as Indo-Pacific humpback dolphins, face amplified threats from overlapping demersal fishing and contaminant hotspots, reducing suitability by up to 20% in modeled Asian ranges. Despite regulatory efforts like gear modifications and observer programs, underreporting and illegal fishing persist, hindering precise global quantification.

Effects of Climate Change on Populations

Ocean warming, driven by anthropogenic , alters marine thermal regimes, prompting distributional shifts in dolphin species toward poleward latitudes or deeper waters to track suitable conditions. For instance, the (Lagenorhynchus obliquidens) has exhibited a poleward range expansion in the northeastern Pacific, correlating with a 1–2°C rise in sea surface temperatures since the 1980s, as evidenced by sighting data from 1991–2005 compared to historical records. Similarly, bottlenose dolphins (Tursiops truncatus) in certain regions have adjusted diets from sardines to due to warming-induced prey mismatches, reducing efficiency and caloric intake. Prey availability disruptions exacerbate these effects, as climate-driven changes in ocean currents and stratification reduce primary productivity and shift , compelling dolphins to expend more energy migrating or adapting strategies. In coastal ecosystems, estuarine species like Indo-Pacific humpback dolphins (Sousa chinensis) face compounded declines, with populations dropping from over 1,000 to 742 individuals in recent decades, partly attributable to prey scarcity from warming and synergies. , projected to decrease seawater pH by 0.3–0.4 units by 2100 under high-emission scenarios, further impairs calcifying prey such as and pteropods at the base of food webs, indirectly stressing dolphin nutrition. Extreme weather events, intensified by , disrupt dolphin habitats and elevate mortality; tropical cyclones have been linked to mass strandings and in vulnerable coastal populations, with post-storm prey displacements persisting for weeks. Oceanic dolphins, such as striped dolphins (Stenella coeruleoalba), show lower vulnerability due to wider ranges, but coastal and resident groups risk genetic isolation from fragmented distributions, diminishing resilience. in warming oceans compounds challenges, as hypoxic zones expand, forcing dolphins into riskier surface behaviors and increasing susceptibility, including respiratory pathogens tracked via seasonal migrations. Overall, while short-term range expansions may buffer some , long-term projections indicate habitat compression for tropical dolphins, with empirical models forecasting 20–50% range losses in equatorial zones by mid-century.

Conservation and Management

The International Union for Conservation of Nature (IUCN) assesses cetacean species, including dolphins, with 26% of the 92 evaluated species classified as threatened (Critically Endangered, Endangered, or Vulnerable) as of 2021 assessments. This proportion has risen from 15% in 1991 and 19% in 2008, reflecting worsening statuses for 20% of species between 2008 and 2021, with only three species improving. Oceanic dolphins (family Delphinidae) generally fare better than coastal or riverine species, many of which face elevated risks in due to , loss, and ; however, globally abundant species like the (Tursiops truncatus) remain Least Concern, while subspecies such as the Maui dolphin (Cephalorhynchus hectori maui) are Critically Endangered. Population trends vary widely by species and region, with some oceanic populations stable or growing—such as North Atlantic short-beaked s (Delphinus delphis) estimated at 640,000 individuals—while others exhibit documented declines. For instance, populations in the Mediterranean and Black Seas have undergone substantial reductions due to fishery interactions, and Bay of Biscay s show a 2.4% annual decline amid ongoing threats. River dolphins, including Irrawaddy dolphins (Orcaella brevirostris) in the , have declined at 1.6% annually from 2007 to 2015, contributing to a broader 73% drop in freshwater cetacean numbers since the 1980s. Critically low populations, like the Maui dolphin's estimated fewer than 50 individuals as of 2021, continue a 3% annual decline since 1985, underscoring localized risks despite global cetacean abundances exceeding millions for common species.
Selected Dolphin SpeciesIUCN Status (Global)Key Population Trend Notes
Common bottlenose (Tursiops truncatus)Least ConcernStable to increasing in many coastal areas; regional declines from . Wait, no specific URL, but from trends. Actually, avoid if not direct.
Wait, better not table if citations tricky; use prose.
These trends highlight that while human pressures drive declines in vulnerable populations, data deficiencies persist for many , complicating precise global extrapolations.

Conservation Strategies and Successes

Conservation strategies for dolphins emphasize mitigating anthropogenic threats, particularly in fisheries, habitat degradation, and direct exploitation. Under frameworks like the U.S. (MMPA) and the International Dolphin Conservation Program (IDCP), measures include mandatory use of acoustic deterrents such as pingers on gillnets to repel dolphins, gear modifications like excluder devices in trawls to allow escape, and time-area fishing closures in high-interaction zones. These approaches aim to keep incidental mortality below potential biological removal (PBR) levels, calculated as half the maximum population growth rate times minimum population estimate. For river dolphins, such as the Ganges and Amazon species, strategies involve establishing protected river sections, enforcing gillnet bans, and community-based monitoring to curb and from dams. Habitat-focused efforts include designating marine protected areas (MPAs) and reducing inputs, with rehabilitation programs for stranded individuals incorporating veterinary protocols to boost rates post-release. The "dolphin-safe" labeling scheme, enforced via the Dolphin Protection Consumer Information Act, prohibits labeling for from purse-seine sets encircling dolphins, supported by onboard observers verifying no intentional encirclement or observed deaths. International cooperation through conventions like and CMS facilitates trade restrictions on and migratory protections, though enforcement varies by region. Notable successes include the stabilization of eastern tropical Pacific (ETP) stocks following IDCP implementation in the 1990s, which reduced observed fishery-related mortality from over 100,000 annually in the 1960s- to under 2,000 by the 2010s, allowing populations to persist at sustainable levels despite not fully recovering to pre-exploitation abundance. In , protections for Hector's dolphins, including trawl and gillnet bans in key areas since the , have slowed decline rates, with photo-identification studies showing persistent but stable local groups. For Irrawaddy dolphins in , fisher-led acoustic monitoring and temporary gillnet closures have garnered local support and confirmed reduced interactions, contributing to halted declines in surveyed subpopulations as of 2023. However, these gains are fragile, as unobserved and cumulative stressors like continue to impede broader recoveries, with many species showing growth rates below the 4% maximum potential due to depressed reproductive success.

Recent Developments and Challenges (Post-2020)

A 2021 IUCN assessment found that 26% of the world's cetacean , encompassing dolphins, face extinction risk, up from 19% in 2008, with riverine and coastal species in particularly vulnerable due to and fisheries interactions. This update incorporated post-2020 data reflecting accelerated threats from and , though critics note IUCN assessments may underemphasize recovery in managed populations due to reliance on academic surveys prone to sampling biases. Bycatch persists as the leading direct anthropogenic mortality factor, with European fisheries data through 2023 documenting frequent entanglements in static nets, where common dolphins comprised a significant portion of incidents despite mitigation efforts like gear modifications. Global estimates from 2025 indicate annual cetacean in the hundreds of thousands, concentrated in purse-seine and gillnet fisheries, undermining population recovery even as some U.S. fisheries achieved over 99% reductions via observer programs and gear tech since the 1980s baseline. Mass strandings have surged post-2020, including a 2023 event involving one of the largest fatal incidents in decades, attributed to navigational errors compounded by and algal toxins, and record beaching in 2024 linked to prey shifts from warming waters disrupting foraging patterns. Investigations into these events reveal multifactorial causes, including exposure and ingestion, with 2025 analyses implicating chemical runoff and vessel traffic increases. Population metrics show strain, as a 2025 study of North Atlantic common dolphins reported lifespan declines—females dying up to 10 years earlier than historical norms—and a 2.4% growth rate drop from 1997-2019, signaling cumulative stress from prey scarcity and contaminants. Similarly, Indo-Pacific humpback dolphins declined from over 1,000 to 742 individuals in recent decades, driven by and habitat loss, per 2025 modeling. In , Ganges River dolphin necropsies from 2008-2024 indicated ~50% of deaths tied to fisheries entanglement, with post-2020 enforcement gaps exacerbating declines. Conservation advances include the 2022-2023 designation of 43 new Important Areas (IMMAs) in the North West Atlantic and to curb shipping and overlaps, informed by acoustic and tracking data. National strategies, such as Nepal's 2021-2025 Ganges dolphin plan, emphasize real-time monitoring via community patrols and , yielding localized sighting increases but limited basin-wide impact amid pollution. Challenges persist in implementation, as rising global shipping—up 20-30% post-pandemic—intensifies collision risks without uniform international regs.

Debates on Sustainable Harvesting vs. Strict Protection

The debate over sustainable harvesting of dolphins versus strict protection revolves around small cetacean hunts, particularly drive fisheries targeting species like pilot whales in the and various dolphins in . Proponents of sustainable harvesting assert that regulated takes from abundant populations provide cultural, nutritional, and economic benefits without threatening long-term viability, drawing parallels to managed fisheries. In the , the grindadráp hunt averages around 800 long-finned pilot whales annually, representing less than 1% of the estimated North Atlantic population of approximately 250,000 individuals, with Faroese officials maintaining that community-driven monitoring ensures sustainability. Japan's Taiji hunts, capturing or killing 200-300 dolphins yearly, are defended by local fishermen as traditional practices on resilient stocks like striped dolphins, with takes deemed negligible compared to global fish harvests. Opponents, including environmental organizations, contend that such hunts lack sufficient population data for many , risking depletion of data-deficient stocks and disrupting social structures through methods like drive herding, which induce stress across entire pods. The (IWC) does not regulate small cetacean harvesting but highlights conservation concerns, noting unknown impacts from directed takes on declining populations. Critics also point to high mercury and PCB levels in pilot whale meat, undermining nutritional claims and raising human health risks, as documented in Faroese health advisories since 2008 recommending limited consumption. Strict protection advocates emphasize dolphins' cognitive complexity and ecological roles, arguing that bans under frameworks like the U.S. Marine Mammal Protection Act (MMPA) have stabilized populations where enforced, and that sustainable harvesting quotas are unenforceable for migratory, hard-to-census species. Reports from groups like the Environmental Investigation Agency assert Japan's small cetacean hunts are unsustainable due to inadequate monitoring and bycatch overlaps, advocating phase-outs over cultural exemptions. Pro-harvesting perspectives counter that absolute bans ignore indigenous rights and local knowledge, potentially fostering illegal poaching, as seen in regions with enforcement gaps. Empirical assessments vary by species; for instance, Northeast Atlantic pilot whales show stable trends despite hunts, while some Pacific dolphin stocks exhibit declines linked to combined anthropogenic pressures. Post-2020 developments, including record Faroese harvests like 1,428 pilot whales in 2023, have intensified calls for international oversight, with petitions exceeding 294,000 signatures urging cessation, though locals frame the practice as integral to amid global vulnerabilities. Truth-seeking analyses prioritize stock-specific modeling over blanket policies, recognizing that while some abundant odontocete populations tolerate low-level directed takes, broader threats like necessitate precautionary approaches to avoid irreversible losses in vulnerable taxa.

Human-Dolphin Interactions

Historical Exploitation and Cultural Significance

Humans have exploited dolphins for , , and other resources since . Archaeological evidence from a 6000-year-old site in Panama's reveals patterns of dolphin procurement for meat and possibly other uses, indicating early subsistence hunting in the Pacific. In the Black Sea region, exploitation of cetaceans including dolphins persisted continuously for approximately 8500 years, from the era through historic periods, as evidenced by remains and tool analyses. These practices involved coastal communities targeting dolphins for their nutritional value and materials like for . In , dolphin fishing traces to traditional coastal practices, with drive hunts in Taiji linked to broader whaling customs originating in the (1603–1868). Systematic documentation of Taiji's annual hunts intensified in the , particularly from 1969 onward with the establishment of captive trade via the Taiji Whale Museum, leading to combined slaughter for meat and selection for aquariums. Quotas set by Japanese fisheries have permitted catches of species like striped and bottlenose dolphins, with historical records showing near-quota fulfillment, such as around 1400 slaughtered in the 2007–2008 season. Similar drive hunting methods persist in regions like and the , where dolphins are harvested for meat and teeth. Dolphins occupied prominent roles in ancient cultural and mythological narratives, often symbolizing benevolence and maritime protection. Minoan frescoes from Akrotiri on Thera, dating to the , depict dolphins amid seascapes, underscoring their significance in Aegean society as emblems of the sea's vitality. In , dolphins served as messengers for and rescuers of humans; the legend of , a from Lesbos active in the (circa 625 BC), describes his salvation from murderous sailors by a dolphin drawn to his music, a tale recorded by in the . Dolphins appeared frequently on ancient coinage, such as the silver from Tarentum minted between 290 and 280 BC, portraying them as symbols of prosperity and naval power. Roman traditions extended these motifs, viewing dolphins as guides for souls to the and emblems of safe voyages. In medieval European heraldry, the dolphin featured in the arms of the Dauphin of Viennois from the , representing swiftness and grace. These enduring depictions highlight dolphins' dual perception as both utilitarian resources and sacred or auspicious figures across civilizations, uninfluenced by modern conservation ethics.

Captivity: Welfare Evidence and Practices

Dolphins in , primarily bottlenose (Tursiops truncatus), are housed in s and aquariums for public display, interactive programs, and research, with practices governed by regulations such as the U.S. Animal Welfare Act (). Enclosures must meet minimum horizontal dimensions (MHD) of 7.32 meters (24 feet) or twice the average adult length of the dolphin for single animals, with required volumes starting at 37.85 cubic meters (1,336 cubic feet) and increasing by at least 75 cubic meters (2,657 cubic feet) per additional cetacean in group settings. These standards aim to provide space for and diving, though critics argue they remain insufficient compared to wild ranging patterns spanning kilometers daily. Training employs positive reinforcement techniques during daily sessions tied to feeding, promoting behaviors for performances and health checks. Welfare assessments rely on behavioral, physiological, and health indicators, with empirical studies revealing mixed outcomes influenced by enclosure design and management. Stereotypic behaviors, such as repetitive pacing, unidirectional circling, and self-inflicted beaching on platforms, are documented in captive dolphins and linked to environmental restriction and boredom, serving as markers of compromised welfare under chronic stress models. Physiological data, including cortisol levels from blood and fecal analyses, indicate variable stress responses, with some facilities showing elevated indicators during training anticipation or confinement, though enrichment programs like toys and social grouping can mitigate these. Behavioral diversity studies suggest that while captivity limits natural foraging and ranging, structured activities may enhance certain affiliative interactions absent in impoverished wild comparisons. Survival and data provide quantifiable welfare insights, with a of U.S. zoological bottlenose dolphins from onward reporting median lifespans of 29.2 years and annual rates of 0.97, comparable to or exceeding wild estimates where environmental hazards like predation and reduce averages to around 20-40 years. First-year mortality has declined to 8-26% post-1990 due to veterinary advancements, though wild-born captives exhibit lower overall than facility-born ones, highlighting acclimation challenges. Independent reviews question these metrics' sufficiency, noting that extended lifespans may mask psychological distress from unnatural and spatial constraints, as evidenced by higher and raking incidents in confined groups. Industry sources, often affiliated with associations like the Alliance of Marine Mammal Parks and Aquariums, emphasize welfare improvements through larger habitats and non-invasive monitoring, yet organizations cite persistent evidence of suffering, urging phase-outs based on ethical and empirical grounds. Peer-reviewed syntheses underscore the need for validated metrics beyond survival, such as validated anticipatory behaviors and stereotypic prevalence, to causally link conditions to outcomes, revealing that while medical care extends , core needs for vast, dynamic environments remain unmet in most facilities.

Military and Research Applications

The United States Navy's Marine Mammal Program, initiated in 1959, trains (Tursiops truncatus) primarily for detecting underwater threats such as sea mines and enemy divers in harbor defense operations. Dolphins leverage their natural echolocation abilities, which outperform mechanical in detecting small objects in turbid waters or cluttered environments, to mark targets with buoys or retrieve objects. The program expanded from initial studies of dolphin sonar capabilities in 1960 to operational deployments, including during the in the 1960s and the Persian Gulf conflicts in the 1980s and 1990s, where dolphins located over 100 mines. Similar efforts occurred in the during the , with the navy training dolphins near in the Black Sea for tasks including attacking combat divers using harpoon-equipped harnesses or detecting submarines. Following the USSR's dissolution in 1991, the program transitioned; some dolphins were acquired by , but reestablished capabilities, deploying trained dolphins to protect naval bases, as evidenced by in April 2022 showing pens near occupied amid the ongoing conflict. These applications highlight dolphins' utility in asymmetric , where their speed, agility, and sensory precision provide advantages over technology alone, though ethical concerns regarding persist without altering operational efficacy. In research contexts, dolphins serve as model organisms for studying echolocation and , yielding insights applicable to engineering and . Experiments demonstrate dolphins can echolocate continuously for up to 15 days, accurately detecting and reporting targets, which informs designs for autonomous underwater vehicles requiring persistent vigilance. Cross-modal perception studies reveal dolphins form mental representations of object shapes via echoes alone, akin to tactile or visual processing, advancing understanding of sensory integration and potential human prosthetic technologies. Brain imaging research contrasts echolocating cetaceans' auditory processing with non-echolocators, elucidating neural adaptations that enhance naval acoustic detection systems. These findings stem from controlled lab settings, emphasizing empirical advantages of biological sensors over synthetic alternatives in complex marine environments.

Therapeutic Interventions: Claims vs. Empirical Outcomes

Dolphin-assisted therapy (DAT) involves structured interactions between humans, typically children with developmental or psychological conditions, and captive dolphins, purportedly to enhance cognitive, emotional, and social functioning. Proponents, including facilities in and , claim DAT yields rapid improvements in symptoms of autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and depression, attributing benefits to dolphins' echolocation, playfulness, or motivational effects. These assertions often stem from anecdotal reports and small-scale studies funded or conducted by therapy providers, raising concerns about conflicts of interest and in source selection. Empirical evaluations, however, reveal persistent methodological shortcomings across decades of research. A 2012 review of 16 DAT studies for ASD and related conditions found none employed randomized controlled designs, with samples averaging under 20 participants, lacking blinding, and relying on subjective parent reports prone to expectancy effects. Short-term gains, such as temporary mood elevation, were observed but indistinguishable from responses or the novelty of marine environments, with no sustained benefits post-intervention. Similarly, a 2021 updated of over 20 studies reaffirmed these flaws, noting inadequate controls for variables like increased therapist attention or vacation-like settings, and concluding DAT offers no evidence-based advantages over conventional behavioral therapies. Controlled trials underscore the gap between claims and outcomes. A 2012 study of 28 children with ASD reported no significant improvements in autism severity or theory-of-mind skills after dolphin sessions compared to land-based controls, despite some behavioral play gains attributable to unstructured interaction rather than dolphin-specific factors. Proponent research, such as a 2019 examination claiming enhanced verbal synchrony in ASD children during DAT, suffered from non-random assignment and absence of comparison groups, limiting causal inferences. Systematic critiques highlight risks, including zoonotic infections from dolphin contact and ethical concerns over animal stress, with no peer-reviewed data supporting DAT's superiority or unique mechanisms like "sonic healing." Overall, rigorous syntheses from independent reviewers, including those in Anthrozoös and journals, determine DAT lacks empirical validation as a therapeutic modality, with observed effects better explained by non-specific factors like human-animal bonding or environmental change rather than dolphin intervention. Costs, often exceeding $5,000 per week-long program, amplify opportunity costs against evidence-based alternatives like , which demonstrate replicable gains in randomized trials. While some families report subjective satisfaction, this aligns with dynamics rather than verifiable efficacy, underscoring the need for skepticism toward unsubstantiated claims in animal-assisted interventions.

Commercial Uses Including Fishing and Culinary Practices

Dolphins face commercial exploitation through targeted for , , and bait in select regions, though such practices remain limited globally and often controversial due to population impacts and ethical concerns. In , coastal hunts including the Taiji drive fishery capture up to 20,000 dolphins, porpoises, and small whales annually via hand harpoons, drive methods, and small-type , yielding and other products. National quotas for small cetacean catches reached 10,920 in fiscal year 2023, primarily targeting species like striped and bottlenose dolphins. Actual harvests in Taiji have trended downward since the 2010s, with the 2023/24 season recording fewer slaughters and captures amid declining domestic demand. Culinary use of dolphin meat persists as a traditional practice in parts of , where it features in regional dishes despite low national popularity and health risks from high mercury levels—tests showing concentrations up to 100 times safe limits in samples from Taiji. The meat, dense and dark red, is consumed locally or sold, sometimes mislabeled as other to boost marketability. In , dolphins are illegally hunted for both consumption and as bait in longline and gillnet fisheries, with thousands killed yearly along the coast; this represents the world's largest unreported dolphin harvest, driven by demand in small-scale operations. Beyond targeted hunts, dolphins encounter incidental mortality as bycatch in global commercial fisheries, where entanglement in gear like gillnets and purse seines claims over 300,000 cetaceans annually, though utilization of bycaught individuals varies by region and is often prohibited or underreported. In West African nations, small cetaceans including dolphins are increasingly taken for food and bait amid economic pressures, contributing to hunts exceeding 100,000 individuals yearly across multiple countries. These practices, while providing protein or fishery inputs in resource-limited areas, lack comprehensive regulation in many cases, exacerbating depletion risks for vulnerable populations.

References

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