Cetacea

Cetacea Temporal range: 53.5–0 Ma PreꞒ Ꞓ O S D C P T J K Pg N Early Eocene – Present
Sperm whale Humpback whale Orca North Atlantic right whale Amazon river dolphin Harbor porpoise
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Class:	Mammalia
Order:	Artiodactyla
Clade:	Cetaceamorpha
Infraorder:	Cetacea Brisson, 1762
Subgroups
†Pakicetidae †Ambulocetidae †Remingtonocetidae †Protocetidae (paraphyletic) Pelagiceti Uhen, 2008[1] †Basilosauridae (paraphyletic) †Kekenodontidae Neoceti Fordyce & de Muizon, 2001[2] Mysticeti Odontoceti (see text for families)
Diversity
Around 94 species

Cetacea (/sɪˈteɪʃə/; from Latin cetus 'whale', from Ancient Greek κῆτος (kêtos) 'huge fish, sea monster')^[3] is an infraorder of aquatic mammals belonging to the order Artiodactyla that includes whales, dolphins and porpoises. Key characteristics are their fully aquatic lifestyle, streamlined body shape, often large size and exclusively carnivorous diet. They propel themselves through the water with powerful up-and-down movement of their tail which ends in a paddle-like fluke, using their flipper-shaped forelimbs to maneuver.^[4]

While the majority of cetaceans live in marine environments, a small number reside solely in brackish water or fresh water. Having a cosmopolitan distribution, they can be found in some rivers and all of Earth's oceans, and many species inhabit vast ranges where they migrate with the changing of the seasons.

Cetaceans are famous for their high intelligence, complex social behaviour, and the enormous size of some of the group's members. For example, the blue whale reaches a maximum confirmed length of 29.9 meters (98 feet) and a weight of 173 tonnes (190 short tons), making it the largest animal ever known to have existed.^[5][6][7]

There are approximately 89^[8] living species split into two parvorders: Odontoceti or toothed whales (containing porpoises, dolphins, other predatory whales like the beluga and the sperm whale, and the poorly understood beaked whales) and the filter feeding Mysticeti or baleen whales (which includes species like the blue whale, the humpback whale and the bowhead whale). Despite their highly modified bodies and carnivorous lifestyle, genetic and fossil evidence places cetaceans as nested within even-toed ungulates, most closely related to hippopotamus within the clade Whippomorpha.

Cetaceans have been extensively hunted for their meat, blubber and oil by commercial operations. Although the International Whaling Commission has agreed on putting a halt to commercial whaling, whale hunting is still going on, either under IWC quotas to assist the subsistence of Arctic native people or in the name of scientific research, although a large spectrum of non-lethal methods are now available to study marine mammals in the wild.^[9] Cetaceans also face severe environmental hazards from underwater noise pollution, entanglement in abandoned ropes and nets, collisions with ships, plastic and heavy metals build-up, to accelerating climate change,^[10][11] but how much they are affected varies widely from species to species, from minimally in the case of the southern bottlenose whale to the baiji (Chinese river dolphin) which is considered to be functionally extinct due to human activity.^[12]

Baleen whales and toothed whales

Skull of the North Atlantic right whale (Mysticeti)

Skull of the orca (Odontoceti)

The two parvorders, baleen whales (Mysticeti) and toothed whales (Odontoceti), are thought to have diverged around thirty-four million years ago.^[13]

Baleen whales have bristles made of keratin instead of teeth. The bristles filter krill and other small invertebrates from seawater. Grey whales feed on bottom-dwelling mollusks. Rorqual family (balaenopterids) use throat pleats to expand their mouths to take in food and sieve out the water. Balaenids (right whales and bowhead whales) have massive heads that can make up 40% of their body mass. Most mysticetes prefer the food-rich colder waters of the Northern and Southern Hemispheres, migrating to the Equator to give birth. During this process, they are capable of fasting for several months, relying on their fat reserves.

The parvorder of Odontocetes – the toothed whales – include sperm whales, beaked whales, orcas, dolphins and porpoises. Generally their teeth have evolved to catch fish, squid or other marine invertebrates, not for chewing them, so prey is swallowed whole. Teeth are shaped like cones (dolphins and sperm whales), spades (porpoises), pegs (belugas), tusks (narwhals) or variable (beaked whale males). Female beaked whales' teeth are hidden in the gums and are not visible, and most male beaked whales have only two short tusks. Narwhals have vestigial teeth other than their tusk, which is present on males and 15% of females and has millions of nerves to sense water temperature, pressure and salinity. A few toothed whales, such as some orcas, feed on mammals, such as pinnipeds and other whales.

Toothed whales have well-developed senses – their eyesight and hearing are adapted for both air and water, and they have advanced sonar capabilities using their melon. Their hearing is so well-adapted for both air and water that some blind specimens can survive. Some species, such as sperm whales, are well adapted for diving to great depths. Several species of toothed whales show sexual dimorphism, in which the males differ from the females, usually for purposes of sexual display or aggression.

Anatomy

Dolphin anatomy

Cetacean bodies are generally similar to those of fish, which can be attributed to their lifestyle and the habitat conditions. Their body is well-adapted to their habitat, although they share essential characteristics with other higher mammals (Eutheria).^[14]

They have a streamlined shape, and their forelimbs are flippers. Almost all have a dorsal fin on their backs, but this can take on many forms, depending on the species. A few species, such as the beluga whale, lack them. Both the flipper and the fin are for stabilization and steering in the water.^{[citation needed]}

The male genitals and the mammary glands of females are sunken into the body.^[15][16] The male genitals are attached to a vestigial pelvis.^[17]

The body is wrapped in a thick layer of fat, known as blubber. This provides thermal insulation and gives cetaceans their smooth, streamlined body shape. In larger species, it can reach a thickness up to one-half meter (1.6 feet).^{[citation needed]}

Sexual dimorphism evolved in many toothed whales. Sperm whales, narwhals, many members of the beaked whale family, several species of the porpoise family, orcas, pilot whales, eastern spinner dolphins and northern right whale dolphins show this characteristic.^[18] Males in these species developed external features absent in females that are advantageous in combat or display. For example, male sperm whales are up to 63% percent larger than females, and many beaked whales possess tusks used in competition among males.^[18][19] Hind legs are not present in cetaceans, nor are any other external body attachments such as a pinna and hair.^[20]

Head

Head profile of a beluga whale, featuring the large "melon" region

Close up of a feeding humpback whale, showing baleen

Whales have an elongated head, especially baleen whales, due to the wide overhanging jaw. Bowhead whale plates can be 9 metres (30 ft) long. Their nostril(s) make up the blowhole, with one in toothed whales and two in baleen whales.^[21]

The nostrils are located on top of the head above the eyes so that the rest of the body can remain submerged while surfacing for air. The back of the skull is significantly shortened and deformed. By shifting the nostrils to the top of the head, the nasal passages extend perpendicularly through the skull.^[22] The teeth or baleen in the upper jaw sit exclusively on the maxilla. The braincase is concentrated through the nasal passage to the front and is correspondingly higher, with individual cranial bones that overlap.^{[citation needed]}

In toothed whales, connective tissue exists in the melon as a head buckle. This is filled with air sacs and fat that aid in buoyancy and biosonar. The sperm whale has a particularly pronounced melon; this is called the spermaceti organ and contains the eponymous spermaceti, hence the name "sperm whale". Even the long tusk of the narwhal is a vice-formed tooth. In many toothed whales, the depression in their skull is due to the formation of a large melon and multiple, asymmetric air bags.^{[citation needed]}

River dolphins, unlike most other cetaceans, can turn their head 90°. Most other cetaceans have fused neck vertebrae and are unable to turn their head at all.^{[citation needed]}

The baleen of baleen whales consists of long, fibrous strands of keratin. Located in place of the teeth, it has the appearance of a huge fringe and is used to sieve the water for plankton and krill.^{[citation needed]}

Brain

Brain of the sperm whale, considered the largest brain in the world

Sperm whales have the largest brain mass of any animal on Earth, averaging 8,000 cm³ (490 in³) and 7.8 kg (17 lb) in mature males.^[23] The brain to body mass ratio in some odontocetes, such as belugas and narwhals, is second only to humans.^[24] In some whales, however, it is less than half that of humans: 0.9% versus 2.1%.^{[citation needed]}

In cetaceans, evolution in the water has caused changes to the head that have modified brain shape such that the brain folds around the insula and expands more laterally than in terrestrial mammals. As a result, the cetacean prefrontal cortex (compared to that in humans) rather than frontal is laterally positioned.^[25]

Brain size was previously considered a major indicator of intelligence. 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 cognitive tasks. Allometric analysis of the relationship between mammalian brain mass (weight) and body mass for different species of mammals shows that larger species generally have larger brains. However, this increase is not fully proportional. Typically the brain mass only increases in proportion to somewhere between the two-thirds power (or the square of the cube root) and the three-quarters power (or the cube of the fourth root) of the body mass. m_brain ∝ (m_body)^k where k is between two-thirds and three-quarters. Thus if Species B is twice the size of Species A, its brain size will typically be somewhere between 60% and 70% higher.^[26] Comparison of a particular animal's brain size with the expected brain size based on such an analysis provides an encephalization quotient that can be used as an indication of animal intelligence.^[27]

The neocortex of many cetaceans is home to elongated spindle neurons that, prior to 2019, were known only in hominids.^[28] In humans, these cells are thought to be involved in social conduct, emotions, judgment and theory of mind.^[29] Cetacean spindle neurons are found in areas of the brain homologous to where they are found in humans, suggesting they perform a similar function.^[30]

Skeleton

Diagram featuring the typical skeletal of a toothed whale (top) and a baleen whale (bottom)

The cetacean skeleton is largely made up of cortical bone, which stabilizes the animal in the water. For this reason, the usual terrestrial compact bones, which are finely woven cancellous bone, are replaced with lighter and more elastic material. In many places, bone elements are replaced by cartilage and even fat, thereby improving their hydrostatic qualities. The ear and the muzzle contain a bone shape that is exclusive to cetaceans with a high density, resembling porcelain. This conducts sound better than other bones, thus aiding biosonar.

The number of vertebrae that make up the spine varies by species, ranging from forty to ninety-three. The cervical spine, found in all mammals, consists of seven vertebrae which, however, are reduced or fused. This fusion provides stability during swimming at the expense of mobility. The fins are carried by the thoracic vertebrae, ranging from nine to seventeen individual vertebrae. The sternum is cartilaginous. The last two to three pairs of ribs are not connected and hang freely in the body wall. The stable lumbar and tail include the other vertebrae. Below the caudal vertebrae is the chevron bone.

The front limbs are paddle-shaped with shortened arms and elongated finger bones, to support movement. They are connected by cartilage. The second and third fingers display a proliferation of the finger members, a so-called hyperphalangy. The shoulder joint is the only functional joint in all cetaceans except for the Amazon river dolphin. The collarbone is completely absent.

Fluke

Humpback whale fluke

Cetaceans have a cartilaginous fluke at the end of their tails that is used for propulsion. The fluke is set horizontally on the body and used with vertical movements, unlike fish and ichthyosaurs, which have vertical tails which move horizontally.^[31]

Physiology

Circulation

Cetaceans have powerful hearts. Blood oxygen is distributed effectively throughout the body. They are warm-blooded, i.e., they hold a nearly constant body temperature.^[32]

Respiration

Cetaceans have lungs, meaning they breathe air. An individual can last without a breath from a few minutes to over two hours depending on the species. Cetacea are deliberate breathers who must be awake to inhale and exhale. When stale air, warmed from the lungs, is exhaled, it condenses as it meets colder external air. As with a terrestrial mammal breathing out on a cold day, a small cloud of 'steam' appears. This is called the 'spout' and varies across species in shape, angle and height. Species can be identified at a distance using this characteristic.

The structure of the respiratory and circulatory systems is of particular importance for the life of marine mammals. The oxygen balance is effective. Each breath can replace up to 90% of the total lung volume. For land mammals, in comparison, this value is usually about 15%. During inhalation, about twice as much oxygen is absorbed by the lung tissue as in a land mammal. As with all mammals, the oxygen is stored in the blood and the lungs, but in cetaceans, it is also stored in various tissues, mainly in the muscles. The muscle pigment, myoglobin, provides an effective bond. This additional oxygen storage is vital for deep diving, since beyond a depth around 100 m (330 ft), the lung tissue is almost completely compressed by the water pressure.

Abdominal organs

The stomach consists of three chambers. The first region is formed by a loose gland and a muscular forestomach (missing in beaked whales); this is followed by the main stomach and the pylorus. Both are equipped with glands to help digestion. A bowel adjoins the stomachs, whose individual sections can only be distinguished histologically. The liver is large and separate from the gall bladder.^[33]

The kidneys are long and flattened. The salt concentration in cetacean blood is lower than that in seawater, requiring kidneys to excrete salt. This allows the animals to drink seawater.^[34] The urinary bladder is proportionally smaller in cetaceans than in land mammals.^[35] The testes are located internally, without an external scrotum.^{[36][37][38][39]} The uterus is bicornuate.^[37]

Senses

Cetacean eyes are set on the sides rather than the front of the head. This means only species with pointed 'beaks' (such as dolphins) have good binocular vision forward and downward. Tear glands secrete greasy tears, which protect the eyes from the salt in the water. The lens is almost spherical, which is most efficient at focusing the minimal light that reaches deep water. Odontocetes have little to no ability to taste or smell, while mysticetes are believed to have some ability to smell because of their reduced, but functional olfactory system.^[40] Cetaceans are known to possess excellent hearing.^[41]

At least one species, the tucuxi or Guiana dolphin, is able to use electroreception to sense prey.^[42]

Ears

Biosonar

The external ear has lost the pinna (visible ear), but still retains a narrow ear canal. The three small bones or ossicles that transmit sound within each ear are dense and compact, and differently shaped from those of land mammals. The semicircular canals are much smaller relative to body size than in other mammals.^[43]

A bony structure of the middle and inner ear, the auditory bulla, is composed of two compact and dense bones (the periotic and tympanic). It is housed in a cavity in the middle ear; in the Odontoceti (apart from in the physeterids, this cavity is filled with dense foam and completely surrounds the bulla, which is connected to the skull only by ligaments. This may isolate the ear from sounds transmitted through the bones of the skull, something that also happens in bats.^[44]

Cetaceans use sound to communicate, using groans, moans, whistles, clicks or the 'singing' of the humpback whale.^[42]

Echolocation

Odontoceti are generally capable of echolocation.^[45] They can discern the size, shape, surface characteristics, distance and movement of an object. They can search for, chase and catch fast-swimming prey in total darkness. Most Odontoceti can distinguish between prey and nonprey (such as humans or boats); captive Odontoceti can be trained to distinguish between, for example, balls of different sizes or shapes. Echolocation clicks also contain characteristic details unique to each animal, which may suggest that toothed whales can discern between their own click and that of others.^[46]

While differences in ear structure associated with echolocating abilities are found amongst Cetacea, cranial asymmetry has also been found to be a factor in the ability to produce sounds used in echolocation. Mysticeti, who don't have the ability to echolocate, possess general symmetry of the skull and facial region, while Odontoceti display a nasofacial asymmetry that is linked to their echolocating abilities. ^[47] Differences in the level of asymmetry also seem to correlate with differences in the types of sounds produced.^[48]

Mysticeti have exceptionally thin, wide basilar membranes in their cochleae without stiffening agents, making their ears adapted for processing low to infrasonic frequencies.^[49]

Chromosomes

The initial karyotype includes a set of chromosomes from 2n = 44. They have four pairs of telocentric chromosomes (whose centromeres sit at one of the telomeres), two to four pairs of subtelocentric and one or two large pairs of submetacentric chromosomes. The remaining chromosomes are metacentric—the centromere is approximately in the middle—and are rather small. All cetaceans have chromosomes 2n = 44, except the sperm whales and pygmy sperm whales, which have 2n = 42.^[50]

Ecology

Range and habitat

See also: Cetaceans of the Caribbean

Cetaceans are found in many aquatic habitats. While many marine species, such as the blue whale, the humpback whale and the orca, have a distribution area that includes nearly the entire ocean, some species occur only locally or in broken populations. These include the vaquita, which inhabits a small part of the Gulf of California and Hector's dolphin, which lives in some coastal waters in New Zealand. Most river dolphin species live exclusively in fresh water.^[51]

Many species inhabit specific latitudes, often in tropical or subtropical waters, such as Bryde's whale or Risso's dolphin. Others are found only in a specific body of water. The southern right whale dolphin and the hourglass dolphin live only in the Southern Ocean. The narwhal and the beluga live only in the Arctic Ocean. Sowerby's beaked whale and the Clymene dolphin exist only in the Atlantic and the Pacific white-sided dolphin and the northern straight dolphin live only in the North Pacific.^{[citation needed]}

Cosmopolitan species may be found in the Pacific, Atlantic and Indian Oceans. However, northern and southern populations become genetically separated over time. In some species, this separation leads eventually to a divergence of the species, such as produced the southern right whale, North Pacific right whale and North Atlantic right whale.^[52] Migratory species' reproductive sites often lie in the tropics and their feeding grounds in polar regions.

Thirty-two species are found in European waters, including twenty-five toothed and seven baleen species.^{[citation needed]}

Whale migration

Many species of whales migrate on a latitudinal basis to move between seasonal habitats. For example, the gray whale migrates 10,000 miles (16,000 km) round trip. The journey begins at winter birthing grounds in warm lagoons along Baja California, and traverses 5,000–7,000 miles (8,000–11,300 km) of coastline to summer feeding grounds in the Bering, Chuckchi and Beaufort seas off the coast of Alaska.^[53]

Behaviour

Sleep

Conscious breathing cetaceans sleep but cannot afford to be unconscious for long, because they may drown. While knowledge of sleep in wild cetaceans is limited, toothed cetaceans in captivity have been recorded to exhibit unihemispheric slow-wave sleep (USWS), which means they sleep with one side of their brain at a time, so that they may swim, breathe consciously and avoid both predators and social contact during their period of rest.^[54]

A 2008 study found that sperm whales sleep in vertical postures just under the surface in passive shallow 'drift-dives', generally during the day, during which whales do not respond to passing vessels unless they are in contact, leading to the suggestion that whales possibly sleep during such dives.^[55]

Diving

See also: Physiology of underwater diving § Mammals

While diving, the animals reduce their oxygen consumption by lowering the heart activity and blood circulation; individual organs receive no oxygen during this time. Some rorquals can dive for up to 40 minutes, sperm whales between 60 and 90 minutes and bottlenose whales for two hours. Diving depths average about 100 m (330 ft). Species such as sperm whales can dive to 3,000 m (9,800 ft), although more commonly 1,200 metres (3,900 ft).^[56][57]

Social relations

Most cetaceans are social animals, although a few species live in pairs or are solitary. A group, known as a pod, usually consists of ten to fifty animals, but on occasion, such as mass availability of food or during mating season, groups may encompass more than one thousand individuals. Inter-species socialization can occur.^[58]

Pods have a fixed hierarchy, with the priority positions determined by biting, pushing or ramming. The behavior in the group is aggressive only in situations of stress such as lack of food, but usually it is peaceful. Contact swimming, mutual fondling and nudging are common. The playful behavior of the animals, which is manifested in air jumps, somersaults, surfing, or fin hitting, occurs more often than not in smaller cetaceans, such as dolphins and porpoises.^[58]

Whale song

Males in some baleen species communicate via whale song, sequences of high pitched sounds. These "songs" can be heard for hundreds of kilometers. Each population generally shares a distinct song, which evolves over time. Sometimes, an individual can be identified by its distinctive vocals, such as the 52-hertz whale that sings at a higher frequency than other whales. Some individuals are capable of generating over 600 distinct sounds.^[58] In baleen species such as humpbacks, blues and fins, male-specific song is believed to be used to attract and display fitness to females.^[59]

Hunting

Pod groups also hunt, often with other species. Many species of dolphins accompany large tunas on hunting expeditions, following large schools of fish. The orca hunts in pods and targets belugas and even larger whales. Humpback whales, among others, form in collaboration bubble carpets to herd krill or plankton into bait balls before lunging at them.^[58]

Intelligence

Main article: Cetacean intelligence

Bubble net feeding

Cetacea are known to teach, learn, cooperate, scheme and grieve.^[60]

Smaller cetaceans, such as dolphins and porpoises, engage in complex play behavior, including such things as producing stable underwater toroidal air-core vortex rings or "bubble rings". The two main methods of bubble ring production are rapid puffing of air into the water and allowing it to rise to the surface, forming a ring, or swimming repeatedly in a circle and then stopping to inject air into the helical vortex currents thus formed. They also appear to enjoy biting the vortex rings, so that they burst into many separate bubbles and then rise quickly to the surface. Whales produce bubble nets to aid in herding prey.^[61]

Killer whale porpoising

Larger whales are also thought to engage in play. The southern right whale elevates its tail fluke above the water, remaining in the same position for a considerable time. This is known as "sailing". It appears to be a form of play and is most commonly seen off the coast of Argentina and South Africa.^[62] Humpback whales also display this behaviour.^{[citation needed]}

Self-awareness appears to be a sign of abstract thinking. Self-awareness, although not well-defined, is believed to be a precursor to more advanced processes such as metacognitive reasoning (thinking about thinking) that humans exploit. Dolphins appear to possess self-awareness.^[63] The most widely used test for self-awareness in animals is the mirror test, in which a temporary dye is placed on an animal's body and the animal is then presented with a mirror. Researchers then explore whether the animal shows signs of self-recognition.^[64]

Critics claim that the results of these tests are susceptible to the Clever Hans effect. This test is much less definitive than when used for primates. Primates can touch the mark or the mirror, while dolphins cannot, making their alleged self-recognition behavior less certain. Skeptics argue that behaviors said to identify self-awareness resemble existing social behaviors, so researchers could be misinterpreting self-awareness for social responses. Advocates counter that the behaviors are different from normal responses to another individual. Dolphins show less definitive behavior of self-awareness, because they have no pointing ability.^[64]

In 1995, Marten and Psarakos used video to test dolphin self-awareness.^[65] They showed dolphins real-time footage of themselves, recorded footage and another dolphin. They concluded that their evidence suggested self-awareness rather than social behavior. While this particular study has not been replicated, dolphins later "passed" the mirror test.^[64]

Decision-making

Collective decisions are an important part of life as a cetacean for the many species that spend time in groups (whether these be temporary such as the fission-fusion dynamics of many smaller dolphin species or long-term stable associations as are seen in killer whale and sperm whale matrilines). ^[66] Little is known about how these decisions work, though studies have found evidence messy consensus decisions in groups of sperm whales and leadership in other species like bottlenose dolphins and killer whales.^{[citation needed]}

Life history

Reproduction and brooding

Most cetaceans sexually mature at seven to 10 years. An exception to this is the La Plata dolphin, which is sexually mature at two years, but lives only to about 20. The sperm whale reaches sexual maturity within about 20 years and has a lifespan between 50 and 100 years.^[58]

For most species, reproduction is seasonal. Ovulation coincides with male fertility. This cycle is usually coupled with seasonal movements that can be observed in many species. Most toothed whales have no fixed bonds. In many species, females choose several partners during a season. Baleen whales are largely monogamous within each reproductive period.^{[citation needed]}

Gestation ranges from 9 to 16 months. Duration is not necessarily a function of size. Porpoises and blue whales gestate for about 11 months. As with all mammals other than marsupials and monotremes, the embryo is fed by the placenta, an organ that draws nutrients from the mother's bloodstream. Mammals without placentas either lay minuscule eggs (monotremes) or bear minuscule offspring (marsupials).^{[citation needed]}

Cetaceans usually bear one calf. In the case of twins, one usually dies, because the mother cannot produce sufficient milk for both. In modern cetaceans, the fetus is usually positioned for a tail-first delivery. Contrary to popular belief, this is not to minimize the risk of drowning during delivery. More likely it has to do with the mechanics of birthing and the shape of the fetus.^[67] After birth, the mother carries the infant to the surface for its first breath. At birth, they are about one-third of their adult length and tend to be independently active, comparable to terrestrial mammals.^{[citation needed]}

Suckling

Like other placental mammals, cetaceans give birth to well-developed calves and nurse them with milk from their mammary glands. When suckling, the mother actively splashes milk into the mouth of the calf, using the muscles of her mammary glands, as the calf has no lips. This milk usually has a high-fat content, ranging from 16 to 46%, causing the calf to increase rapidly in size and weight.^[58]

In many small cetaceans, suckling lasts for about four months. In large species, it lasts for over a year and involves a strong bond between mother and offspring.^{[citation needed]}

The mother is solely responsible for brooding. In some species, so-called "aunts" occasionally suckle the young.^{[citation needed]}

This reproductive strategy provides a few offspring that have a high survival rate.^{[citation needed]}

Lifespan

Among cetaceans, whales are distinguished by an unusual longevity compared to other higher mammals. Some species, such as the bowhead whale (Balaena mysticetus), can reach over 200 years. Based on the annual rings of the bony otic capsule, the age of the oldest known specimen is a male determined to be 211 years at the time of death.^[68]

Death

Main article: Whale fall

Upon death, whale carcasses fall to the deep ocean and provide a substantial habitat for marine life. Evidence of whale falls in present-day and fossil records shows that deep-sea whale falls support a rich assemblage of creatures, with a global diversity of 407 species, comparable to other neritic biodiversity hotspots, such as cold seeps and hydrothermal vents.^[69]

Deterioration of whale carcasses happens through three stages. Initially, organisms such as sharks and hagfish scavenge the soft tissues at a rapid rate over a period of months and as long as two years. This is followed by the colonization of bones and surrounding sediments (which contain organic matter) by enrichment opportunists, such as crustaceans and polychaetes, throughout a period of years. Finally, sulfophilic bacteria reduce the bones releasing hydrogen sulfide enabling the growth of chemoautotrophic organisms, which in turn, support organisms such as mussels, clams, limpets and sea snails. This stage may last for decades and supports a rich assemblage of species, averaging 185 per site.^[69][70]

Disease

Brucellosis affects almost all mammals. It is distributed worldwide, while fishing and pollution have caused porpoise population density pockets, which risks further infection and disease spreading. Brucella ceti, most prevalent in dolphins, has been shown to cause chronic disease, increasing the chance of failed birth and miscarriages, male infertility, neurobrucellosis, cardiopathies, bone and skin lesions, strandings and death. Until 2008, no case had ever been reported in porpoises, but isolated populations have an increased risk and consequentially a high mortality rate.^[71]

Evolution

Main article: Evolution of cetaceans

Fossil history

Origins

The direct ancestors of today's cetaceans are probably found within the Dorudontidae whose most famous member, Dorudon, lived at the same time as Basilosaurus. Both groups had already developed some of the typical anatomical features of today's whales, such as the fixed bulla, which replaces the mammalian eardrum, as well as sound-conducting elements for submerged directional hearing. Their wrists were stiffened and probably contributed to the typical build of flippers. The hind legs existed, however, but were significantly reduced in size and with a vestigial pelvis connection.^[72]

Transition from land to sea

Fossil of a Maiacetus (red, beige skull) with fetus (blue, red teeth) shortly before the end of gestation ^[73]

The fossil record traces the gradual transition from terrestrial to aquatic life. The regression of the hind limbs allowed greater flexibility of the spine. This made it possible for whales to move around with the vertical tail hitting the water. The front legs transformed into flippers, costing them their mobility on land.^{[citation needed]}

One of the oldest members of ancient cetaceans (Archaeoceti) is Pakicetus from the Middle Eocene of Pakistan. This is an animal the size of a wolf, whose skeleton is known only partially. It had functioning legs and lived near the shore. This suggests the animal could still move on land. The long snout had carnivorous dentition.^[72]

The transition from land to sea dates to about 49 million years ago, with the Ambulocetus ("running whale"), also discovered in Pakistan. It was up to 3 m (9.8 ft) long. The limbs of this archaeocete were leg-like, but it was already fully aquatic, indicating that a switch to a lifestyle independent from land happened extraordinarily quickly.^[74] The snout was elongated with overhead nostrils and eyes. The tail was strong and supported movement through water. Ambulocetus probably lived in mangroves in brackish water and fed in the riparian zone as a predator of fish and other vertebrates.^[75]

Dating from about 45 million years ago are species such as Indocetus, Kutchicetus, Rodhocetus and Andrewsiphius, all of which were adapted to life in water. The hind limbs of these species were regressed and their body shapes resemble modern whales. Protocetidae family member Rodhocetus is considered the first to be fully aquatic. The body was streamlined and delicate with extended hand and foot bones. The merged pelvic lumbar spine was present, making it possible to support the floating movement of the tail. It was likely a good swimmer, but could probably move only clumsily on land, much like a modern seal.^[72]

Marine animals

Since the late Eocene, about 40 million years ago, cetaceans populated the subtropical oceans and no longer emerged on land. An example is the 18 metre long Basilosaurus, sometimes called Zeuglodon. The transition from land to water was completed in about 10 million years. The Wadi Al-Hitan ("Whale Valley") in Egypt contains numerous skeletons of Basilosaurus, as well as other marine vertebrates.^[76]

External phylogeny

Molecular biology, immunology, and fossils show that cetaceans are phylogenetically closely related with the even-toed ungulates (Artiodactyla). Whales' direct lineage began in the early Eocene, around 55.8 million years ago, with early artiodactyls.^[72] Most molecular biological evidence suggests that hippos are the closest living relatives. Common anatomical features include similarities in the morphology of the posterior molars, and the bony ring on the temporal bone (bulla) and the involucre, a skull feature that was previously associated only with cetaceans.^[72] Since the fossil record suggests that the morphologically distinct hippo lineage dates back only about 15 million years, Cetacea and hippos apparently diverged from a common ancestor that was morphologically distinct from either.^[77][78][79] The most striking common feature is the talus, a bone in the upper ankle. Early cetaceans, archaeocetes, show double castors, which occur only in even-toed ungulates. Corresponding findings are from Tethys Sea deposits in northern India and Pakistan. The Tethys Sea was a shallow sea between the Asian continent and northward-bound Indian plate.^{[citation needed]}

Cetaceans evolved convergently as streamlined swimmers with fish and aquatic reptiles.

Molecular and morphological evidence suggests that artiodactyls as traditionally defined are paraphyletic with respect to cetaceans. Cetaceans are deeply nested within the artiodactyls; the two groups together form a clade, a natural group with a common ancestor, for which the name Cetartiodactyla is sometimes used. Modern nomenclature divides Artiodactyla (or Cetartiodactyla) into four subordinate taxa: camelids (Tylopoda), pigs and peccaries (Suina), ruminants (Ruminantia), and hippos plus whales (Whippomorpha). The Cetacea's presumed location within Artiodactyla can be represented in the following cladogram:^{[80][81][82][83][84]}

Artiodactyla	Tylopoda (camels) Artiofabula Suina (pigs) Cetruminantia Ruminantia (ruminants) Tragulidae (mouse deer) Pecora (horn bearers) Cetancodonta/Whippomorpha Hippopotamidae (hippopotamuses) Cetacea (whales) 54 mya

Internal phylogeny

Further information: List of cetaceans and List of extinct cetaceans

Within Cetacea, the two parvorders are baleen whales (Mysticeti) which owe their name to their baleen, and toothed whales (Odontoceti), which have teeth shaped like cones, spades, pegs, or tusks, and can perceive their environment through biosonar.^{[citation needed]}

Relationship of extinct and extant cetaceans[85]:

Raoellidae † Cetacea Pakicetidae † Ambulocetidae † Remingtonocetidae † Rodhocetus † Dorudon † Basilosaurus † Mysticeti Janjucetus † Balaenidae Right whales Neobalaenidae Pygmy right whale Balaenopteridae Rorquals Eschrichtiidae Gray whales (baleen whales, 25 mya) Odontoceti Kogiidae Dwarf sperm whales Physeteridae Sperm whales Platanistidae South Asian river dolphins Ziphiidae Beaked whales Inioidea Lipotidae Yangtze river dolphin Iniidae Pontoporiidae (South American river dolphins) Delphinoidea Delphinidae Oceanic dolphins ("true" dolphins) Monodontidae Belugas & Narwhals Phocoenidae Porpoises (toothed whales)

† Extinct taxa

The terms whale and dolphin are informal:

• Mysticeti:

• Whales, with four families: Balaenidae (right and bowhead whales), Cetotheriidae (pygmy right whales), Balaenopteridae (rorquals), Eschrichtiidae (grey whales)

• Odontoceti:

• Whales: with four families: Monodontidae (belugas and narwhals), Physeteridae (sperm whales), Kogiidae (dwarf and pygmy sperm whales), and Ziphiidae (beaked whales)
• Dolphins, with five families: Delphinidae (oceanic dolphins), Platanistidae (South Asian river dolphins), Lipotidae (old world river dolphins) Iniidae (new world river dolphins), and Pontoporiidae (La Plata dolphins)
• Porpoises, with one family: Phocoenidae

The term 'great whales' covers those currently regulated by the International Whaling Commission:^[86] the Odontoceti families Physeteridae (sperm whales), Ziphiidae (beaked whales), and Kogiidae (pygmy and dwarf sperm whales); and Mysticeti families Balaenidae (right and bowhead whales), Cetotheriidae (pygmy right whales), Eschrichtiidae (grey whales), as well as part of the family Balaenopteridae (minke, Bryde's, sei, blue and fin; not Eden's and Omura's whales).^[87]

Threats

The primary threats to cetaceans come from people, both directly from whaling or drive hunting and indirect threats from fishing and pollution.^[88]

Whaling

Main articles: Whaling, History of Whaling, and Dolphin drive hunting

Methods of whaling

Japanese research ship whaling mother and calf minke whales.

An Atlantic white-sided dolphin caught in a drive hunt in Hvalba on the Faroe Islands being taken away with a forklift.

Whaling is the practice of hunting whales, mainly baleen and sperm whales. This activity has gone on since the Stone Age.^[89]

In the Middle Ages, reasons for whaling included their meat, oil usable as fuel and the jawbone, which was used in house construction. At the end of the Middle Ages, early whaling fleets aimed at baleen whales, such as bowheads. In the 16th and 17th centuries, the Dutch fleet had about 300 whaling ships with 18,000 crewmen.^{[citation needed]}

In the 18th and 19th centuries, baleen whales especially were hunted for their baleen, which was used as a replacement for wood, or in products requiring strength and flexibility such as corsets and crinoline skirts. In addition, the spermaceti found in the sperm whale was used as a machine lubricant and the ambergris as a material for pharmaceutical and perfume industries. In the second half of the 19th century, the explosive harpoon was invented, leading to a massive increase in the catch size.^{[citation needed]}

Large ships were used as "mother" ships for the whale handlers. In the first half of the 20th century, whales were of great importance as a supplier of raw materials. Whales were intensively hunted during this time; in the 1930s, 30,000 whales were killed. This increased to over 40,000 animals per year up to the 1960s, when stocks of large baleen whales collapsed.^{[citation needed]}

Most hunted whales are now threatened, with some great whale populations exploited to the brink of extinction. Atlantic and Korean gray whale populations were completely eradicated and the North Atlantic right whale population fell to some 300–600. The blue whale population is estimated to be around 14,000.^{[citation needed]}

The first efforts to protect whales came in 1931. Some particularly endangered species, such as the humpback whale (which then numbered about 100 animals),^[90] were placed under international protection and the first protected areas were established. In 1946, the International Whaling Commission (IWC) was established, to monitor and secure whale stocks. Whaling of 14 large species for commercial purposes was prohibited worldwide by this organization from 1985 to 2005, though some countries do not honor the prohibition.^{[citation needed]}

Whales caught 2010–2014, by country

The stocks of species such as humpback and blue whales have recovered, though they are still threatened. The United States Congress passed the Marine Mammal Protection Act of 1972 sustain the marine mammal population. It prohibits the taking of marine mammals except for several hundred per year taken in Alaska. Japanese whaling ships are allowed to hunt whales of different species for ostensibly scientific purposes.^{[citation needed]}

Aboriginal whaling is still permitted. About 1,200 pilot whales were taken in the Faroe Islands in 2017,^[91] and about 900 narwhals and 800 belugas per year are taken in Alaska, Canada, Greenland, and Siberia. About 150 minke are taken in Greenland per year, 120 gray whales in Siberia and 50 bowheads in Alaska, as aboriginal whaling, besides the 600 minke taken commercially by Norway, 300 minke and 100 sei taken by Japan and up to 100 fin whales taken by Iceland.^[92] Iceland and Norway do not recognize the ban and operate commercial whaling. Norway and Japan are committed to ending the ban.^{[citation needed]}

Dolphins and other smaller cetaceans are sometimes hunted in an activity known as dolphin drive hunting. This is accomplished by driving a pod together with boats, 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). Dolphins are mostly hunted for their meat, though some end up in dolphinaria. Despite the controversy thousands of dolphins are caught in drive hunts each year.^{[citation needed]}

Fishing

See also: Cetacean bycatch

Dominoes made of baleen

Dolphin pods often reside near large tuna shoals. This is known to fishermen, who look for dolphins to catch tuna. Dolphins are much easier to spot from a distance than tuna, since they regularly breathe. The fishermen pull their nets hundreds of meters wide in a circle around the dolphin groups, in the expectation that they will net a tuna shoal. When the nets are pulled together, the dolphins become entangled under water and drown. Line fisheries in larger rivers are threats to river dolphins.^{[citation needed]}

A greater threat than by-catch for small cetaceans is targeted hunting. In Southeast Asia, they are sold as fish-replacement to locals, since the region's edible fish promise higher revenues from exports. In the Mediterranean, small cetaceans are targeted to ease pressure on edible fish.^[88]

Strandings

Main article: Cetacean stranding

A stranding is when a cetacean leaves the water to lie on a beach. In some cases, groups of whales strand together. The best known are mass strandings of pilot whales and sperm whales. Stranded cetaceans usually die, because their as much as 90 metric tons (99 short tons) body weight compresses their lungs or breaks their ribs. Smaller whales can die of heatstroke because of their thermal insulation.^{[citation needed]}

Beached humpback whale

The causes are not clear. Possible reasons for mass beachings are:^[88]

• toxic contaminants
• debilitating parasites (in the respiratory tract, brain or middle ear)
• infections (bacterial or viral)
• flight from predators (including humans)
• social bonds within a group, so that the pod follows a stranded animal
• disturbance of their magnetic senses by natural anomalies in the Earth's magnetic field
• injuries
• noise pollution by shipping traffic, seismic surveys and military sonar experiments

Since 2000, whale strandings frequently occurred following military sonar testing. In December 2001, the US Navy admitted partial responsibility for the beaching and the deaths of several marine mammals in March 2000. The coauthor of the interim report stated that animals killed by active sonar of some Navy ships were injured. Generally, underwater noise, which is still on the increase, is increasingly tied to strandings; because it impairs communication and sense of direction.^[93]

Climate change influences the major wind systems and ocean currents, which also lead to cetacean strandings. Researchers studying strandings on the Tasmanian coast from 1920 to 2002 found that greater strandings occurred at certain time intervals. Years with increased strandings were associated with severe storms, which initiated cold water flows close to the coast. In nutrient-rich, cold water, cetaceans expect large prey animals, so they follow the cold water currents into shallower waters, where the risk is higher for strandings. Whales and dolphins who live in pods may accompany sick or debilitated pod members into shallow water, stranding them at low tide.^[94]

Environmental hazards

See also: Marine mammals and sonar

Worldwide, use of active sonar has been linked to about 50 marine mammal strandings between 1996 and 2006. In all of these occurrences, there were other contributing factors, such as unusual (steep and complex) underwater geography, limited egress routes, and a specific species of marine mammal—beaked whales—that are suspected to be more sensitive to sound than other marine mammals.

—Rear Admiral Lawrence Rice

Heavy metals, residues of many plant and insect venoms and plastic waste flotsam are not biodegradable. Sometimes, cetaceans consume these hazardous materials, mistaking them for food items. As a result, the animals are more susceptible to disease and have fewer offspring.^[88]

Damage to the ozone layer reduces plankton reproduction because of its resulting radiation. This shrinks the food supply for many marine animals, but the filter-feeding baleen whales are most impacted. Even the Nekton is, in addition to intensive exploitation, damaged by the radiation.^[88]

Food supplies are also reduced long-term by ocean acidification due to increased absorption of increased atmospheric carbon dioxide. The CO₂ reacts with water to form carbonic acid, which reduces the construction of the calcium carbonate skeletons of food supplies for zooplankton that baleen whales depend on.^[88]

The military and resource extraction industries operate strong sonar and blasting operations. Marine seismic surveys use loud, low-frequency sound that show what is lying underneath the Earth's surface.^[95] Vessel traffic also increases noise in the oceans. Such noise can disrupt cetacean behavior such as their use of biosonar for orientation and communication. Severe instances can panic them, driving them to the surface. This leads to bubbles in blood gases and can cause decompression sickness.^[96] Naval exercises with sonar regularly results in fallen cetaceans that wash up with fatal decompression. Sounds can be disruptive at distances of more than 100 kilometres (62 mi). Damage varies across frequency and species.^{[citation needed]}

Relationship to humans

Research history

See also: Cryptid whale and Whale § In myth, literature and art

A whale as depicted by Conrad Gesner, 1587, in Historiae animalium

In Aristotle's time, the fourth century BCE, whales were regarded as fish due to their superficial similarity. Aristotle, however, observed many physiological and anatomical similarities with the terrestrial vertebrates, such as blood (circulation), lungs, uterus and fin anatomy.^[97] His detailed descriptions were assimilated by the Romans, but mixed with a more accurate knowledge of the dolphins, as mentioned by Pliny the Elder in his Natural history. In the art of this and subsequent periods, dolphins are portrayed with a high-arched head (typical of porpoises) and a long snout. The harbour porpoise was one of the most accessible species for early cetologists; because it could be seen close to land, inhabiting shallow coastal areas of Europe. Much of the findings that apply to all cetaceans were first discovered in porpoises.^[98] One of the first anatomical descriptions of the airways of a harbor porpoise dates from 1671 by John Ray. It nevertheless referred to the porpoise as a fish.^[99][100]

The tube in the head, through which this kind fish takes its breath and spitting water, located in front of the brain and ends outwardly in a simple hole, but inside it is divided by a downward bony septum, as if it were two nostrils; but underneath it opens up again in the mouth in a void.

— John Ray, 1671, the earliest description of cetacean airways

In the 10th edition of Systema Naturae (1758), Swedish biologist and taxonomist Carl Linnaeus asserted that cetaceans were mammals and not fish. His groundbreaking binomial system formed the basis of modern whale classification.^{[citation needed]}

Culture

Cetaceans have played a role in human culture through history.^{[citation needed]}

Prehistoric

Stone Age petroglyphs, such as those in Roddoy and Reppa (Norway), and the Bangudae Petroglyphs in South Korea, depict them.^[101][102] Whale bones were used for many purposes. In the Neolithic settlement of Skara Brae on Orkney sauce pans were made from whale vertebrae.^{[citation needed]}

Antiquity

Destruction of Leviathan; engraving by Gustave Doré, 1865

Silver coin with Taras riding a dolphin

The whale was first mentioned in ancient Greece by Homer. There, it is called Ketos, a term that initially included all large marine animals. From this was derived the Roman word for whale, Cetus. Other names were phálaina (Aristotle, Latin form of ballaena) for the female and, with an ironic characteristic style, musculus (Mouse) for the male. North Sea whales were called Physeter, which was meant for the sperm whale Physter macrocephalus. Whales are described in particular by Aristotle, Pliny and Ambrose. All mention both live birth and suckling. Pliny describes the problems associated with the lungs with spray tubes and Ambrose claimed that large whales would take their young into their mouth to protect them.

In the Bible especially, the leviathan plays a role as a sea monster. The essence, which features a giant crocodile or a dragon and a whale, was created according to the Bible by God^[103] and should again be destroyed by him.^[104][105] In the Book of Job, the leviathan is described in more detail.^[106][107]

In Jonah there is a more recognizable description of a whale alongside the prophet Jonah, who, on his flight from the city of Nineveh, is swallowed by a whale.

Dolphins are mentioned far more often than whales. Aristotle discusses the sacred animals of the Greeks in his Historia Animalium and gives details of their role as aquatic animals. The Greeks admired the dolphin as a "king of the aquatic animals" and referred to them erroneously as fish. Its intelligence was apparent both in its ability to escape from fishnets and in its collaboration with fishermen.

River dolphins are known from the Ganges and—erroneously—the Nile. In the latter case it was equated with sharks and catfish. Supposedly they attacked even crocodiles.

Dolphins appear in Greek mythology. Because of their intelligence, they rescued multiple people from drowning. They were said to love music, probably because of their own song, and in the legends they saved famous musicians, such as Arion of Lesbos from Methymna.

Constellation Cetus

Dolphins belong to the domain of Poseidon and led him to his wife Amphitrite. Dolphins are associated with other gods, such as Apollo, Dionysus and Aphrodite. The Greeks paid tribute to both whales and dolphins with their own constellation. The constellation of the Whale (Ketos, lat. Cetus) is located south of the Dolphin (Delphi, lat. Delphinus) north of the zodiac.

Ancient art often included dolphin representations, including the Cretan Minoans. Later they appeared on reliefs, gems, lamps, coins, mosaics and gravestones. A particularly popular representation is that of Arion or Taras riding on a dolphin. In early Christian art, the dolphin is a popular motif, at times used as a symbol of Christ.

Middle Ages to the 19th century

See also: History of Whaling and Cryptid whales

St. Brendan described in his travel story Navigatio Sancti Brendani an encounter with a whale, between the years 565–573. He described how he and his companions entered a treeless island, which turned out to be a giant whale, which he called Jasconicus. He met this whale seven years later and rested on his back.^{[citation needed]}

Most descriptions of large whales from this time until the whaling era, beginning in the 17th century, were of beached whales, which resembled no other animal. This was particularly true for the sperm whale, the most frequently stranded in larger groups. Raymond Gilmore documented seventeen sperm whales in the estuary of the Elbe from 1723 to 1959 and thirty-one animals on the coast of Great Britain in 1784. In 1827, a blue whale beached itself off the coast of Ostend. Whales were used as attractions in museums and traveling exhibitions.^{[citation needed]}

Depiction of baleen whaling, 1840

Stranded sperm whale engraving, 1598

Whalers from the 17th to 19th centuries depicted whales in drawings and recounted tales of their occupation. Although they knew that whales were harmless giants, they described battles with harpooned animals. These included descriptions of sea monsters, including huge whales, sharks, sea snakes, giant squid and octopuses.^{[citation needed]}

Among the first whalers who described their experiences on whaling trips was Captain William Scoresby from Great Britain, who published the book Northern Whale Fishery, describing the hunt for northern baleen whales. This was followed by Thomas Beale, a British surgeon, in his book Some observations on the natural history of the sperm whale in 1835; and Frederick Debell Bennett's The tale of a whale hunt in 1840. Whales were described in narrative literature and paintings, most famously in the novels Moby Dick by Herman Melville and Twenty Thousand Leagues Under the Seas by Jules Verne.^{[citation needed]}

Baleen was used to make vessel components such as the bottom of a bucket in the Scottish National Museum. The Norsemen crafted ornamented plates from baleen, sometimes interpreted as ironing boards.^{[citation needed]}

In the Canadian Arctic (east coast) in Punuk and Thule culture (1000–1600 C.E.),^[108] baleen was used to construct houses in place of wood as roof support for winter houses, with half of the building buried under the ground. The actual roof was probably made of animal skins that were covered with soil and moss.^[109]

Modern culture

Further information: Whale § Interactions with humans

Sea World show featuring bottlenose dolphins and false killer whales

In the 20th century, perceptions of cetaceans changed. They transformed from monsters into creatures of wonder, as science revealed them to be intelligent and peaceful animals. Hunting was replaced by whale and dolphin tourism. This change is reflected in films and novels. For example, the protagonist of the series Flipper was a bottle-nose dolphin. The TV series SeaQuest DSV (1993–1996), the movies Free Willy and Star Trek IV: The Voyage Home, and the book series The Hitchhiker's Guide to the Galaxy by Douglas Adams are examples.^[110]

The study of whale song also produced a popular album, Songs of the Humpback Whale.^{[citation needed]}

Captivity

Whales and dolphins have been kept in captivity for use in education, research and entertainment since the 19th century.^{[citation needed]}

Belugas

Main article: Beluga whale § Captivity

Beluga whales were the first whales to be kept in captivity. Other species were too rare, too shy or too big. The first was shown at Barnum's Museum in New York City in 1861.^[111] For most of the 20th century, Canada was the predominant source.^[112] They were taken from the St. Lawrence River estuary until the late 1960s, after which they were predominantly taken from the Churchill River estuary until capture was banned in 1992.^[112] Russia then became the largest provider.^[112] Belugas are caught in the Amur Darya delta and their eastern coast and are transported domestically to aquaria or dolphinaria in Moscow, St. Petersburg and Sochi, or exported to countries such as Canada.^[112] They have not been domesticated.^[113]

As of 2006, 30 belugas lived in Canada and 28 in the United States. 42 deaths in captivity had been reported.^[112] A single specimen can reportedly fetch up to US$100,000 (£64,160). The beluga's popularity is due to its unique color and its facial expressions. The latter is possible because while most cetacean "smiles" are fixed, the extra movement afforded by the beluga's unfused cervical vertebrae allows a greater range of apparent expression.^[114]

Orcas

Main article: Captive killer whales

See also: SeaWorld § Criticism and resulting impact, and Incidents at SeaWorld parks

Ulises the orca, 2009

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, fifty-five whales were taken from the wild in Iceland, nineteen 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 forty-eight animals on display in the world were captive-born.^[115]

Organizations such as World Animal Protection and the Whale and Dolphin Conservation campaign against the practice of keeping them in captivity.^{[citation needed]}

In captivity, they often develop pathologies, such as the dorsal fin collapse seen in 60–90% of captive males. Captives have reduced life expectancy, on average only living into their 20s, although some live longer, including several over 30 years old and two, Corky II and Lolita, in their mid-40s. In the wild, females who survive infancy live 46 years on average and up to 70–80 years. Wild males who survive infancy live 31 years on average and can reach 50–60 years.^[116]

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 orca 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.^[117] Captives occasionally act aggressively towards themselves, their tankmates, or humans, which critics say is a result of stress.^[118] Orcas are well known for their performances in shows, but the number of orcas kept in captivity is small, especially when compared to the number of bottlenose dolphins, with only forty-four captive orcas being held in aquaria as of 2012.^[119]

Each country has its own tank requirements; in the US, the minimum enclosure size is set by the Code of Federal Regulations, 9 CFR E § 3.104, under the Specifications for the Humane Handling, Care, Treatment and Transportation of Marine Mammals.^[120]

Dawn Brancheau doing a show four years before the incident

Aggression among captive orcas is common. They attack each other and their trainers as well. In 2013, SeaWorld's treatment of orcas in captivity was the basis of the movie Blackfish, which documents the history of Tilikum, an orca at SeaWorld Orlando, who had been involved in the deaths of three people.^[121] The film led to proposals by some lawmakers to ban captivity of cetaceans, and led SeaWorld to announce in 2016 that it would phase out its orca program after various unsuccessful attempts to restore its revenues, reputation, and stock price.^[122]

Others

SeaWorld pilot whale with trainers

Dolphins and porpoises are kept in captivity. Bottlenose dolphins are the most common, as they are relatively easy to train, have a long lifespan in captivity and have a friendly appearance. 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. There are also fewer than ten pilot whales, Amazon river dolphins, Risso's dolphins, spinner dolphins, or tucuxi in captivity. Two unusual and rare hybrid dolphins, known as wolphins, are kept at Sea Life Park in Hawaii, which is a cross between a bottlenose dolphin and a false killer whale. Also, two common/bottlenose hybrids reside in captivity at Discovery Cove and SeaWorld San Diego.^{[citation needed]}

In repeated attempts in the 1960s and 1970s, narwhals kept in captivity died within months. A breeding pair of pygmy right whales were retained in a netted area. They were eventually released in South Africa. In 1971, SeaWorld captured a California gray whale calf in Mexico at Scammon's Lagoon. The calf, later named Gigi, was separated from her mother using a form of lasso attached to her flukes. Gigi was displayed at SeaWorld San Diego for a year. She was then released with a radio beacon affixed to her back; however, contact was lost after three weeks. Gigi was the first captive baleen whale. JJ, another gray whale calf, was kept at SeaWorld San Diego. JJ was an orphaned calf that beached itself in April 1997 and was transported two miles to SeaWorld. The 680 kilograms (1,500 lb) calf was a popular attraction and behaved normally, despite separation from his mother. A year later, the then 8,164.7 kilograms (18,000 lb) whale though smaller than average, was too big to keep in captivity, and was released on April 1, 1998. A captive Amazon river dolphin housed at Acuario de Valencia is the only trained river dolphin in captivity.^[123][124]

Here is a list of all the cetaceans that have been taken into captivity for either conservation, research or human entertainment and education purposes currently or in the past, temporarily or permanently.^{[citation needed]}

• Atlantic white-sided dolphin
• Baiji
• Beluga whale
• Boto
• Bottlenose dolphin
• Commerson's dolphin
• Common dolphin
• False killer whale
• Finless porpoise
• Gray whale
• Harbour porpoise
• Indo-Pacific humpback dolphin
• Irrawaddy dolphin
• Long-finned pilot whale
• Melon-headed whale
• Minke whale
• Narwhal
• Orca
• Pacific white-sided dolphin
• Pygmy killer whale
• Pygmy sperm whale
• Risso's dolphin
• Rough-toothed dolphin
• Short-finned pilot whale
• South Asian river dolphin
• Spinner dolphin
• Spotted dolphin
• Tucuxi
• Vaquita
• Wholphin

References

1. Uhen, M.D. (2008). "New protocetid whales from Alabama and Mississippi, and a new Cetacean clade, Pelagiceti". Journal of Vertebrate Paleontology. 28 (3): 589–593. doi:10.1671/0272-4634(2008)28[589:NPWFAA]2.0.CO;2. JSTOR 20490986. S2CID 86326007.
2. Fordyce, E.; de Muizon, C. (2001). "Evolutionary history of the cetaceans: a review". In Mazin, J.-M.; de Buffrénil, V. (eds.). Secondary Adaptations of Tetrapods to Life in the Water: Proceedings of the international meeting, Poitiers, 1996. München, Germany: Verlag Dr. Friedrich Pfeil. pp. 169–233. ISBN 3-931516-88-1. LCCN 2002550356. OCLC 52121251. OL 20591860M.
3. M. Raneft, D.; Eaker, H.; W. Davis, R. (2001). "A guide to the pronunciation and meaning of cetacean taxonomic names" (PDF). Aquatic Mammals. 27 (2): 185. Archived (PDF) from the original on 2016-03-27.
4. E. Fish, Frank (2002). "Balancing Requirements for Stability and Maneuverability in Cetaceans". Integrative and Comparative Biology. 42 (1): 85–93. doi:10.1093/icb/42.1.85. PMID 21708697. S2CID 25036870.
5. Wood, Gerald The Guinness Book of Animal Facts and Feats (1983) ISBN 978-0-85112-235-9
6. Davies, Ella (2016-04-20). "The longest animal alive may be one you never thought of". BBC Earth. Retrieved 2018-02-14.
7. "Largest mammal". Guinness World Records.
8. Perrin, W.F. (2020). "World Cetacea Database". marinespecies.org. Retrieved 2020-12-12.
9. Notarbartolo di Sciara, G.; Briand, F. (2004). "Investigating the Roles of Cetaceans in Marine Ecosystems - An overview". CIESM Workshop Monographs. 25: 1–15.[1]
10. Cara E. Miller (2007). Current State of Knowledge of Cetacean Threats, Diversity, and Habitats in the Pacific Islands Region (PDF). Whale and Dolphin Conservation Society. ISBN 978-0-646-47224-9. Archived from the original (PDF) on 8 September 2015. Retrieved 5 September 2015.
11. Nowacek, Douglas; Donovan, Greg; Gailey, Glenn; Racca, Roberto; Reeves, Randall; Vedenev, Alexander; Weller, David; Southall, Brandon (2013). "Responsible Practices for Minimizing and Monitoring Environmental Impacts of Marine Seismic Surveys with an Emphasis on Marine Mammal". Aquatic Mammals. 39 (4): 356–377. doi:10.1578/am.39.4.2013.356.
12. Lovgren, Stefan (December 14, 2006). "China's Rare River Dolphin Now Extinct, Experts Announce". National Geographic News. Washington, D.C.: National Geographic Society. Archived from the original on December 18, 2006. Retrieved 2015-10-18.
13. Cerchio, Salvatore; Tucker, Priscilla (1998-06-01). "Influence of Alignment on the mtDNA Phylogeny of Cetacea: Questionable Support for a Mysticeti/Physeteroidea Clade". Systematic Biology. 47 (2): 336–344. doi:10.1080/106351598260941. ISSN 1076-836X. PMID 12064231. S2CID 16270218.
14. Groves; Colin; Grubb, Peter (2011). "Ungulate taxonomy". JHU Press. ^{[page needed]}
15. Thewissen, J.G.M. (11 November 2013). The Emergence of Whales: Evolutionary Patterns in the Origin of Cetacea. Springer. pp. 383–. ISBN 978-1-4899-0159-0.
16. Miller, Debra Lee (2007). Reproductive Biology and Phylogeny of Cetacea: Whales, Porpoises and Dolphins. CRC Press. ISBN 978-1-4398-4257-7.
17. Tinker, Spencer Wilkie (1988-01-01). Whales of the World. Brill Archive. ISBN 978-0-935848-47-2.
18. Dines, James; Mesnick, Sarah; Ralls, Katherine; May-Collado, Laura; Agnarsson, Ingi; Dean, Matthew (2015). "A trade-off between precopulatory and postcopulatory trait investment in male cetaceans". Evolution. 69 (6): 1560–1572. doi:10.1111/evo.12676. PMID 25929734. S2CID 18292677.
19. Dalebout, Merel; Steel, Debbie; Baker, Scott (2008). "Phylogeny of the Beaked Whale Genus Mesoplodon (Ziphiidae: Cetacea) Revealed by Nuclear Introns: Implications for the Evolution of Male Tusks". Systematic Biology. 57 (6): 857–875. doi:10.1080/10635150802559257. PMID 19085329. S2CID 205729032.
20. "How ancient whales lost their legs, got sleek and conquered the oceans". EurekAlert. University of Florida. 2006-05-22. Retrieved 2016-03-20.
21. Buono, Mónica R.; Fernández, Marta S.; Fordyce, R. Ewan; Reidenberg, Joy S. (2015). "Anatomy of nasal complex in the southern right whale, Eubalaena australis (Cetacea, Mysticeti)". Journal of Anatomy. 226 (1): 81–92. doi:10.1111/joa.12250. ISSN 1469-7580. PMC 4313901. PMID 25440939.
22. Milan Klima (29 January 1999). Development of the Cetacean Nasal Skull. Springer. ISBN 978-3-540-64996-0. ^{[page needed]}
23. "Sperm Whales brain size". NOAA Fisheries – Office of Protected Resources. Retrieved 9 August 2015.
24. Fields, R. Douglas. "Are whales smarter than we are?". Scientific American. Retrieved 9 August 2015.
25. Gerussi, Tommaso; Graïc, Jean-Marie; Peruffo, Antonella; Behroozi, Mehdi; Schlaffke, Lara; Huggenberger, Stefan; Güntürkün, Onur; Cozzi, Bruno (2023). "The prefrontal cortex of the bottlenose dolphin (Tursiops truncatus Montagu, 1821): a tractography study and comparison with the human". Brain Structure and Function. 228 (8): 1963–1976. doi:10.1007/s00429-023-02699-8. ISSN 1863-2661. PMC 10517040. PMID 37660322.
26. Moore, Jim. "Allometry". University of California San Diego. Retrieved 9 August 2015.
27. Pontarotti, Pierre (2016). Evolutionary Biology: Convergent Evolution, Evolution of Complex Traits. Springer. p. 74. ISBN 978-3-319-41324-2.
28. Watson, K.K.; Jones, T. K.; Allman, J. M. (2006). "Dendritic architecture of the Von Economo neurons". Neuroscience. 141 (3): 1107–1112. doi:10.1016/j.neuroscience.2006.04.084. PMID 16797136. S2CID 7745280.
29. Allman, John M.; Watson, Karli K.; Tetreault, Nicole A.; Hakeem, Atiya Y. (2005). "Intuition and autism: a possible role for Von Economo neurons". Trends Cogn Sci. 9 (8): 367–373. doi:10.1016/j.tics.2005.06.008. PMID 16002323. S2CID 14850316.
30. Hof, Patrick R.; Van Der Gucht, Estel (2007). "Structure of the cerebral cortex of the humpback whale, Megaptera novaeangliae (Cetacea, Mysticeti, Balaenopteridae)". The Anatomical Record. 290 (1): 1–31. doi:10.1002/ar.20407. PMID 17441195. S2CID 15460266.
31. "Why do whale and dolphin tails go up and down?". Whale & Dolphin Conservation USA. Retrieved 2021-12-23.
32. "Whales, dolphins and porpoises". Department of Climate Change, Energy, the Environment and Water. Australian Government Department of Climate Change, Energy, the Environment and Water. Retrieved 19 October 2024.
33. C. Edward Stevens; Ian D. Hume (1995). Comparative Physiology of the Vertebrate Digestive System. University of Cambridge. p. 51. ISBN 978-0-521-44418-7. Retrieved 5 September 2015.
34. Clifford A. Hui (1981). "Seawater Consumption and Water Flux in the Common Dolphin Delphinus delphis". Chicago Journals. 54 (4): 430–440. JSTOR 30155836.
35. John Hunter (26 March 2015). The Works of John Hunter, F.R.S. Cambridge University. p. 35. ISBN 978-1-108-07960-0.
36. Bernd Würsig; J.G.M. Thewissen; Kit M. Kovacs (27 November 2017). Encyclopedia of Marine Mammals. Elsevier Science. ISBN 978-0-12-804381-3. Archived from the original on 29 June 2023. Retrieved 19 October 2020.
37. Rommel, S.A.; Pabst, D.A.; McLellan, W.A. (2007). "Functional anatomy of the cetacean reproductive system, with comparisons to the domestic dog". In Miller, D.L. (ed.). Reproductive Biology and Phylogeny of Cetacea: Whales, Porpoises and Dolphins. pp. 127–145. doi:10.1201/b11001. ISBN 9780429063626.
38. Rommel, S.A.; Pabst, D.A.; McLellan, W.A. (1998). "Reproductive Thermoregulation in Marine Mammals" (PDF). American Scientist. Vol. 86, no. 5. pp. 440–448. JSTOR 27857097. Archived (PDF) from the original on 22 November 2021.
39. Pabst, D.A.; Sentiel, A.R; McLellan, W.A. (1998). "Evolution of thermoregulatory function in cetacean reproductive systems". In Thewissen, J.G.M. (ed.). The Emergence of Whales. Advances in Vertebrate Paleobiology. Springer US. pp. 379–397. doi:10.1007/978-1-4899-0159-0_13. ISBN 978-1-4899-0161-3.
40. Godfrey, Stephen J.; Geisler, Jonathan; Fitzgerald, Erich M. G. (2013). "On the Olfactory Anatomy in an Archaic Whale (Protocetidae, Cetacea) and the Minke Whale Balaenoptera acutorostrata (Balaenopteridae, Cetacea)". The Anatomical Record. 296 (2): 257–272. doi:10.1002/ar.22637. ISSN 1932-8494. PMID 23233318. S2CID 25260840.
41. Mead, James. "Cetacea". Britannica School High. Encyclopædia Britannica, Inc. Retrieved 3 June 2019.
42. Morell, Virginia (July 2011). "Guiana Dolphins Can Use Electric Signals to Locate Prey". Science. American Association for the Advancement of Science (AAAS). Archived from the original on 2013-05-30.
43. Thewissen, J. G. M. (2002). "Hearing". In Perrin, William R.; Wiirsig, Bernd; Thewissen, J. G. M. (eds.). Encyclopedia of Marine Mammals. Academic Press. pp. 570–572. ISBN 978-0-12-551340-1.
44. Ketten, Darlene R. (1992). "The Marine Mammal Ear: Specializations for Aquatic Audition and Echolocation". In Webster, Douglas B.; Fay, Richard R.; Popper, Arthur N. (eds.). The Evolutionary Biology of Hearing. Springer. pp. 717–750. Pages 725–727 used here.
45. Hooker, Sascha K. (2009). Perrin, William F.; Wursig, Bernd; Thewissen, J. G. M. (eds.). Encyclopedia of Marine Mammals (2 ed.). Academic Press. p. 1176. ISBN 978-0-12-373553-9.
46. de Obaldia, C., Simkus, G. & and Zölzer, U. (2015). "Estimating the number of sperm whale (Physeter macrocephalus) individuals based on grouping of corresponding clicks". 41. Jahrestagung für Akustik (DAGA 2015), Nürnberg. doi:10.13140/RG.2.1.3764.9765.
47. Coombs, Ellen J.; Clavel, Julien; Park, Travis; Churchill, Morgan; Goswami, Anjali (2020-07-10). "Wonky whales: the evolution of cranial asymmetry in cetaceans". BMC Biology. 18 (1): 86. doi:10.1186/s12915-020-00805-4. ISSN 1741-7007. PMC 7350770. PMID 32646447.
48. Coombs, Ellen J.; Clavel, Julien; Park, Travis; Churchill, Morgan; Goswami, Anjali (2020-07-10). "Wonky whales: the evolution of cranial asymmetry in cetaceans". BMC Biology. 18 (1): 86. doi:10.1186/s12915-020-00805-4. ISSN 1741-7007. PMC 7350770. PMID 32646447.
49. Ketten, Darlene R. (1997). "Structure and function in whale ears" (PDF). The International Journal of Animal Sound and Its Recording. 8 (1–2): 103–135. Bibcode:1997Bioac...8..103K. doi:10.1080/09524622.1997.9753356. Archived from the original (PDF) on 2014-08-01. Retrieved 2013-12-21.
50. Ulfur Anarson (1974). "Comparative chromosome studies in Cetacea". Institute of Genetics. 77 (1): 1–36. doi:10.1111/j.1601-5223.1974.tb01351.x. PMID 4137586.
51. Cassens, I.; Vicario, S.; Waddell, V.G.; Balchowsky, H.; Van Belle, D.; Ding, W.; Fan, C.; Mohan, R.S.; Simões-Lopes, P.C.; Bastida, R.; Meyer, A.; Stanhope, M.J.; Milinkovitch, M.C. (2000). "Independent adaptation to riverine habitats allowed survival of ancient cetacean lineages". Proceedings of the National Academy of Sciences of the United States of America. 97 (21): 11343–11347. Bibcode:2000PNAS...9711343C. doi:10.1073/pnas.97.21.11343. PMC 17202. PMID 11027333.
52. AR Hoelzel (1998). "Genetic structure of cetacean populations in sympatry, parapatry, and mixed assemblages: implications for conservation policy". Journal of Heredity. 89 (5): 451–458. doi:10.1093/jhered/89.5.451.
53. "Gray Whale Migration". journeynorth.org. Archived from the original on 2019-06-09. Retrieved 3 July 2021.
54. Sekiguchi Y, Arai K, Kohshima S (June 2006). "Sleep behaviour: sleep in continuously active dolphins". Nature. 441 (7096): E9-10, discussion E11. Bibcode:2006Natur.441E...9S. doi:10.1038/nature04898. PMID 16791150. S2CID 4406032.
55. Miller PJ, Aoki K, Rendell LE, Amano M (January 2008). "Stereotypical resting behavior of the sperm whale". Current Biology. 18 (1): R21-3. Bibcode:2008CBio...18..R21M. doi:10.1016/j.cub.2007.11.003. PMID 18177706. S2CID 10587736.
56. Scholander, Per Fredrik (1940). "Experimental investigations on the respiratory function in diving mammals and birds". Hvalraadets Skrifter. 22.
57. Bruno Cozzi; Paola Bagnoli; Fabio Acocella; Maria Laura Costantino (2005). "Structure and biomechanical properties of the trachea of the striped dolphin Stenella coeruleoalba: Evidence for evolutionary adaptations to diving". The Anatomical Record. 284 (1): 500–510. doi:10.1002/ar.a.20182. PMID 15791584.
58. Janet Mann; Richard C. Connor; Peter L. Tyack; et al. (eds.). Cetacean Societies: Field Study of Dolphins and Whales. University of Chicago.
59. Janik, Vincent (2014). "Cetacean vocal learning and communication". Current Opinion in Neurobiology. 28: 60–65. doi:10.1016/j.conb.2014.06.010. PMID 25057816. S2CID 40334723.
60. Siebert, Charles (8 July 2009). "Watching Whales Watching Us". The New York Times Magazine. Retrieved 29 August 2015.
61. Wiley, David; et al. (2011). "Underwater components of humpback whale bubble-net feeding behaviour". Behaviour. 148 (5): 575–602. doi:10.1163/000579511X570893. S2CID 55168063.
62. Carwardine, M. H.; Hoyt, E. (1998). Whales, Dolphins and Porpoises. ISBN 978-0-86449-096-4. {{cite book}}: |journal= ignored (help)
63. "Elephant Self-Awareness Mirrors Humans". Live Science. 30 October 2006. Retrieved 29 August 2015.
64. Derr, Mark (May 2001). "Mirror test". New York Times. Retrieved 3 August 2015.
65. Marten, Ken; Psarakos, Suchi (June 1995). "Using Self-View Television to Distinguish between Self-Examination and Social Behavior in the Bottlenose Dolphin (Tursiops truncatus)". Consciousness and Cognition. 4 (2): 205–224. doi:10.1006/ccog.1995.1026. PMID 8521259. S2CID 44372881.
66. Zwamborn E, Boon N, Whitehead H (October 2023). "Collective Decision-making in Aquatic Mammals". Mammal Review. 53 (4): 238–253. doi:10.1111/mam.12321. S2CID 261141293.
67. Miedema, Feiko; Klein, Nicole; Blackburn, Daniel G.; Sander, P. Martin; Maxwell, Erin E.; Griebeler, Eva M.; Scheyer, Torsten M. (2023-04-18). "Heads or tails first? Evolution of fetal orientation in ichthyosaurs, with a scrutiny of the prevailing hypothesis". BMC Ecology and Evolution. 23 (1): 12. doi:10.1186/s12862-023-02110-4. ISSN 2730-7182. PMC 10114408. PMID 37072698.
68. John C George; Jeffrey Bada; Judith Zeh; Laura Scott; Stephen E Brown; Todd O'Hara; Robert Suydam (1999). "Age and growth estimates of bowhead whales (Balaena mysticetus) via aspartic acid racemization". Canadian Journal of Zoology. 77 (4): 571–580. Bibcode:1999CaJZ...77..571G. doi:10.1139/z99-015.
69. Smith, Craig R.; Baco, Amy R. (2003). Ecology of Whale Falls at the Deep-Sea Floor (PDF). Oceanography and Marine Biology - an Annual Review. Vol. 41. pp. 311–354. doi:10.1201/9780203180594.ch6 (inactive 2024-11-11). ISBN 978-0-415-25462-5. Archived (PDF) from the original on 2006-08-17. Retrieved 23 August 2014.
70. Fujiwara, Yoshihiro; et al. (16 February 2007). "Three-year investigations into sperm whale-fall ecosystems in Japan". Marine Ecology. 28 (1): 219–230. Bibcode:2007MarEc..28..219F. doi:10.1111/j.1439-0485.2007.00150.x.
71. Caterina, Guzmán-Verri; González-Barrientos, Rocío; Hernández-Mora, Gabriela; Morales, Juan-Alberto; Baquero-Calvo, Elías; Chaves-Olarte, Esteban; Moreno, Edgardo (2012). "Brucella ceti and Brucellosis in Cetaceans". Frontiers in Cellular and Infection Microbiology. 2: 3. doi:10.3389/fcimb.2012.00003. PMC 3417395. PMID 22919595.
72. Thewissen, J. G. M.; Cooper, Lisa Noelle; Clementz, Mark T.; Bajpai, Sunil; Tiwari, B. N. (2007). "Whales originated from aquatic artiodactyls in the Eocene epoch of India" (PDF). Nature. 450 (7173): 1190–4. Bibcode:2007Natur.450.1190T. doi:10.1038/nature06343. PMID 18097400. S2CID 4416444. Archived (PDF) from the original on 2013-12-24.
73. Gingerich PD; ul-Haq M; von Koenigswald W; WJ Sanders; Smith BH (2009). "New Protocetid Whale from the Middle Eocene of Pakistan: Birth on Land, Precocial Development, and sexual dimorphism". PLOS ONE. 4 (2): e4366. Bibcode:2009PLoSO...4.4366G. doi:10.1371/journal.pone.0004366. PMC 2629576. PMID 19194487.
74. Ando, Konami; Fujiwara, Shin-ichi (2016-07-10). "Farewell to life on land - thoracic strength as a new indicator to determine paleoecology in secondary aquatic mammals". Journal of Anatomy. 229 (6): 768–777. doi:10.1111/joa.12518. ISSN 0021-8782. PMC 5108153. PMID 27396988.
75. Thewissen, Hans (1994). "Phylogenetic aspects of Cetacean origins: A morphological perspective". Journal of Mammalian Evolution. 2 (3): 157–184. doi:10.1007/bf01473527. S2CID 27675176.
76. "First intact fossil of prehistoric whale discovered in Wadi Al-Hitan". International Union for Conservation of Nature. 9 June 2015.
77. Gatesy, J. (1 May 1997). "More DNA support for a Cetacea/Hippopotamidae clade: the blood-clotting protein gene gamma-fibrinogen". Molecular Biology and Evolution. 14 (5): 537–543. doi:10.1093/oxfordjournals.molbev.a025790. PMID 9159931.
78. Boisserie, Jean-Renaud; Lihoreau, Fabrice; Brunet, Michel (2005). "The position of Hippopotamidae within Cetartiodactyla". Proceedings of the National Academy of Sciences. 102 (5): 1537–1541. Bibcode:2005PNAS..102.1537B. doi:10.1073/pnas.0409518102. PMC 547867. PMID 15677331.
79. "Scientists find missing link between the dolphin, whale and its closest relative, the hippo". Science News Daily. 2005-01-25. Retrieved 2011-01-08.
80. Beck, N.R. (2006). "A higher-level MRP supertree of placental mammals". BMC Evol Biol. 6: 93. doi:10.1186/1471-2148-6-93. PMC 1654192. PMID 17101039.
81. O'Leary, M.A.; Bloch, J.I.; Flynn, J.J.; Gaudin, T.J.; Giallombardo, A.; Giannini, N.P.; et al. (2013). "The placental mammal ancestor and the post-K-Pg radiation of placentals". Science. 339 (6120): 662–667. Bibcode:2013Sci...339..662O. doi:10.1126/science.1229237. hdl:11336/7302. PMID 23393258. S2CID 206544776.
82. Song, S.; Liu, L.; Edwards, S.V.; Wu, S. (2012). "Resolving conflict in eutherian mammal phylogeny using phylogenomics and the multispecies coalescent model". Proceedings of the National Academy of Sciences. 109 (37): 14942–14947. Bibcode:2012PNAS..10914942S. doi:10.1073/pnas.1211733109. PMC 3443116. PMID 22930817.
83. dos Reis, M.; Inoue, J.; Hasegawa, M.; Asher, R.J.; Donoghue, P.C.J.; Yang, Z. (2012). "Phylogenomic datasets provide both precision and accuracy in estimating the timescale of placental mammal phylogeny". Proceedings of the Royal Society B: Biological Sciences. 279 (1742): 3491–3500. doi:10.1098/rspb.2012.0683. PMC 3396900. PMID 22628470.
84. Upham, N.S.; Esselstyn, J.A.; Jetz, W. (2019). "Inferring the mammal tree: Species-level sets of phylogenies for questions in ecology, evolution, and conservation". PLOS Biology. 17 (12): e3000494. doi:10.1371/journal.pbio.3000494. PMC 6892540. PMID 31800571. (see e.g. Fig S10)
85. Gatesy, John; Geisler, Jonathan H.; Chang, Joseph; Buell, Carl; Berta, Annalisa; Meredith, Robert W.; Springer, Mark S.; McGowen, Michael R. (2012). "A phylogenetic blueprint for a modern whale" (PDF). Molecular Phylogenetics and Evolution. 66 (2): 479–506. doi:10.1016/j.ympev.2012.10.012. PMID 23103570. Archived (PDF) from the original on 2013-02-27. Retrieved 4 September 2015.
86. "Small cetaceans". iwc.int. International Whaling Commission. Retrieved 2018-04-08.
87. "Lives of Whales". iwc.int. International Whaling Commission. Retrieved 2018-04-08.
88. Cara E. Miller (2007). Current State of Knowledge of Cetacean Threats, Diversity, and Habitats in the Pacific Islands Region (PDF). Whale and Dolphin Conservation Society. ISBN 978-0-646-47224-9. Archived from the original (PDF) on 8 September 2015. Retrieved 5 September 2015.
89. "Whaling - Commercial, Industrial, Japan | Britannica". Britannica Online Encyclopedia. 2024-10-11. Retrieved 2024-10-28.
90. "A History of the International Whaling Commission (IWC)". wwf.panda.org. Retrieved 2024-08-08.
91. "Hagar & seyðamark". heimabeiti.fo. Archived from the original on 2014-09-24. Retrieved 2018-04-07.
92. "Total Catches". iwc.int. Retrieved 2018-04-07.
93. Schrope, Mark. (2003). "Whale deaths caused by US Navy's sonar". Nature. 415 (106): 106. Bibcode:2002Natur.415..106S. doi:10.1038/415106a. PMID 11805797. S2CID 52827761.
94. Evans, K; Thresher, R; Warneke, R.M; Bradshaw, C.J.A; Pook, M; Thiele, D; Hindell, M.A (2005-06-22). "Periodic variability in cetacean strandings: links to large-scale climate events". Biology Letters. 1 (2): 147–150. doi:10.1098/rsbl.2005.0313. ISSN 1744-9561. PMC 1626231. PMID 17148151.
95. Nowacek, Douglas; Donovan, Greg; Gailey, Glenn; Racca, Roberto; Reeves, Randall; Vedenev, Alexander; Weller, David; Southall, Brandon (2013). "Responsible Practices for Minimizing and Monitoring Environmental Impacts of Marine Seismic Surveys with an Emphasis on Marine Mammal". Aquatic Mammals. 39 (4): 356–377. doi:10.1578/am.39.4.2013.356.
96. M. Andre; T. Johansson; E. Delory; M. van der Schaar (2005). "Cetacean biosonar and noise pollution". Europe Oceans 2005. Vol. 2. Oceans 2005–Europe. pp. 1028–1032 Vol. 2. doi:10.1109/OCEANSE.2005.1513199. ISBN 978-0-7803-9103-1. S2CID 31676969.
97. Aristotle. "Chapter 2". The History of Animals, Book VIII. Translated by Thompson, D'Arcy Wentworth. Archived from the original on April 16, 2022. Retrieved April 16, 2022.
98. Conrad Gesner (6 September 2008). Historiae animalium. Archived from the original on 6 September 2008. Retrieved 4 September 2015.
99. J. Ray (1671). "An account of the dissection of a porpess". Philosophical Transactions of the Royal Society of London. 6 (69–80): 2274–2279. Bibcode:1671RSPT....6.2274R. doi:10.1098/rstl.1671.0048. S2CID 186210473.
100. Susanne Prahl (2007). "Studies for the construction of epicranialen airway when porpoise (Phocoena phocoena Linnaeus, 1758)". Dissertation for the Doctoral Degree of the Department of Biology of the Faculty of Mathematics, Computer Science and Natural Sciences at the University of Hamburg: 6.
101. "PCAS Quarterly - Rock Art on the Channel Islands of California" (PDF).
102. "BBC News - Rock Art Hints at Whaling Origins". 20 April 2004.
103. Psalms 104:26
104. Psalms 74:14
105. Isaiah 27:1.
106. Job 40:25
107. Job 41:26
108. Cunliffe, B.; Gosden, C.; Joyce, R. "The circumpolar zone". The Oxford Handbook of Archaeology.
109. J. Savelle (1997). "The Role of Architectural utility in the formation of archaeological Whale Bone Assemblages". Journal of Archaeological Science. 24 (10): 869–885. Bibcode:1997JArSc..24..869S. doi:10.1006/jasc.1996.0167.
110. unknown. "Movie Retriever: Whales". movieretriever.com. Archived from the original on 2015-10-15.
111. "The Whales, New York Tribune, August 9, 1861". New York Tribune. 9 August 1861. Retrieved 5 December 2011.
112. "Beluga Whales in Captivity: Hunted, Poisoned, Unprotected" (PDF). Special Report on Captivity 2006. Canadian Marine Environment Protection Society. 2006. Archived from the original (PDF) on 26 December 2014. Retrieved 26 December 2014.
113. "Beluga (Delphinapterus leucas) Facts – Distribution – In the Zoo". World Association of Zoos and Aquariums. Archived from the original on 10 February 2012. Retrieved 5 December 2011.
114. Bonner, Nigel (1980). Whales. Facts on File. pp. 17, 23–24. ISBN 978-0-7137-0887-5.
115. NMFS (2005). "Conservation Plan for Southern Resident Killer Whales (Orcinus orca)" (PDF). Seattle, U.S.: National Marine Fisheries Service (NMFS) Northwest Regional Office. pp. 43–44. Archived from the original (PDF) on June 26, 2008. Retrieved January 2, 2009.
116. Rose, N. A. (2011). "Killer Controversy: Why Orcas Should No Longer Be Kept in Captivity" (PDF). Humane Society International and the Humane Society of the United States. Archived (PDF) from the original on 2011-10-26. Retrieved December 21, 2014.
117. "Whale Attack Renews Captive Animal Debate". CBS News. March 1, 2010. Retrieved 6 September 2015.
118. Susan Jean Armstrong (2003). Animal Ethics Reader. Psychology Press. ISBN 978-0-415-27589-7.
119. "Orcas in Captivity – A look at killer whales in aquariums and parks". 23 November 2009. Archived from the original on 2 June 2007. Retrieved 6 September 2015.
120. "Chapter I: Space requirements". Electronic Code of Federal Regulation. 1. Retrieved 6 September 2015.
121. Whiting, Candace Calloway. In the Wake of Blackfish – Is it Time to Retire the Last Killer Whale Whose Capture Was Shown in the Film?", HuffPost, October 29, 2013. Retrieved October 29, 2013.
122. Buss, Dale (2016-03-24). "Shamu Goes Out With the Tide: SeaWorld CEO On Its Abrupt Change – And What Comes Next". Forbes. Retrieved 2016-03-26.
123. Klinowska, Margaret; Cooke, Justin (1991). Dolphins, Porpoises, and Whales of the World: the IUCN Red Data Book (PDF). Archived (PDF) from the original on 2015-05-09. Retrieved 6 September 2015.
124. J. L. Sumich; T. Goff; W. L. Perryman (2001). "Growth of two gray whale calves" (PDF). Aquatic Mammals: 231–233. Archived (PDF) from the original on 2015-10-15. Retrieved 6 September 2015.

External links

• Cetacea at Wikibooks
• "Cetacea" . Encyclopædia Britannica. Vol. 5 (11th ed.). 1911.
• "Cetaceans". Encyclopedia of Earth.
• Scottish Cetacean Research & Rescue – see page on Taxonomy
• "Dolphin and Whale News". Science Daily.
• Futuyma, Douglas J. (1998). "Cetacea Evolution". Archived from the original on 2008-05-29. Retrieved 2007-03-23.
• EIA Cetacean campaign: Reports and latest info.
• EIA in USA: reports etc.