Sperm whale

Last updated

Sperm whale [1]
Temporal range: Pliocene – Recent [2]
O
S
D
C
P
T
J
K
Pg
N
Mother and baby sperm whale.jpg
Sperm-Whale-Scale-Chart-SVG-Steveoc86.svg
CITES Appendix I (CITES) [4]
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Infraorder: Cetacea
Family: Physeteridae
Genus: Physeter
Species:
P. macrocephalus
Binomial name
Physeter macrocephalus
Sperm whale distribution (Pacific equirectangular).jpg
Major sperm whale grounds
Synonyms
  • Physeter catodonLinnaeus, 1758
  • Physeter micropsLinnaeus, 1758
  • Physeter tursioLinnaeus, 1758
  • Physeter australasianus Desmoulins, 1822

The sperm whale or cachalot [lower-alpha 1] (Physeter macrocephalus) is the largest of the toothed whales and the largest toothed predator. It is the only living member of the genus Physeter and one of three extant species in the sperm whale family, along with the pygmy sperm whale and dwarf sperm whale of the genus Kogia .

Contents

The sperm whale is a pelagic mammal with a worldwide range, and will migrate seasonally for feeding and breeding. [5] Females and young males live together in groups, while mature males (bulls) live solitary lives outside of the mating season. The females cooperate to protect and nurse their young. Females give birth every four to twenty years, and care for the calves for more than a decade. A mature sperm whale has no natural predators, although calves and weakened adults are sometimes killed by pods of killer whales (orcas).

Mature males average 16 metres (52 ft) in length, with the head representing up to one-third of the animal's length. Plunging to 2,250 metres (7,382 ft), it is the third deepest diving mammal, exceeded only by the southern elephant seal and Cuvier's beaked whale. [6] [7] The sperm whale uses echolocation and vocalization with source level as loud as 236 decibels (re 1 µPa m) underwater. [8] [9] It has the largest brain on Earth, more than five times heavier than a human's. Sperm whales can live 70 years or more. [10] [11] [12]

Spermaceti (sperm oil), from which the whale derives its name, was a prime target of the whaling industry, and was sought after for use in oil lamps, lubricants, and candles. Ambergris, a solid waxy waste product sometimes present in its digestive system, is still highly valued as a fixative in perfumes, among other uses. Beachcombers look out for ambergris as flotsam. [13] Sperm whaling was a major industry in the 19th century, depicted in the novel Moby-Dick . The species is protected by the International Whaling Commission moratorium, and is listed as vulnerable by the International Union for Conservation of Nature.

Taxonomy and naming

Etymology

The name "sperm whale" is a clipping of "spermaceti whale". Spermaceti, originally mistakenly identified as the whales' semen, is the semi-liquid, waxy substance found within the whale's head. [14] (See "Spermaceti organ and melon" below.)

The sperm whale is also known as the "cachalot", which is thought to derive from the archaic French for 'tooth' or 'big teeth', as preserved for example in the word caishau in the Gascon dialect (a word of either Romance [15] or Basque [16] origin).

The etymological dictionary of Corominas says the origin is uncertain, but it suggests that it comes from the Vulgar Latin cappula 'sword hilts'. [17] The word cachalot came to English via French from Spanish or Portuguese cachalote , perhaps from Galician/Portuguese cachola 'big head'. [18]

The term is retained in the Russian word for the animal, kashalot ( кашалот ), as well as in many other languages.[ citation needed ]

The scientific genus name Physeter comes from the Greek physētēr ( φυσητήρ ), meaning 'blowpipe, blowhole (of a whale)', or – as a pars pro toto – 'whale'.[ citation needed ]

The specific name macrocephalus is Latinized from the Greek makroképhalos ( μακροκέφαλος 'big-headed'), from makros ( μακρός ) + kephalē ( κεφαλή ).[ citation needed ]

Its synonymous specific name catodon means 'down-tooth', from the Greek elements cat(a)- ('below') and odṓn ('tooth'); so named because it has visible teeth only in its lower jaw. [19] (See "Jaws and teeth" below.)

Another synonym australasianus ('Australasian') was applied to sperm whales in the Southern Hemisphere. [20]

Taxonomy

The sperm whale belongs to the order Cetartiodactyla, [21] [22] [23] [24] [25] [ excessive citations ] the order containing all cetaceans and even-toed ungulates. It is a member of the unranked clade Cetacea, with all the whales, dolphins, and porpoises, and further classified into Odontoceti, containing all the toothed whales and dolphins. It is the sole extant species of its genus, Physeter , in the family Physeteridae. Two species of the related extant genus Kogia , the pygmy sperm whale Kogia breviceps and the dwarf sperm whale K. sima, are placed either in this family or in the family Kogiidae. [26] In some taxonomic schemes the families Kogiidae and Physeteridae are combined as the superfamily Physeteroidea (see the separate entry on the sperm whale family). [27]

Swedish ichthyologist Peter Artedi described it as Physeter catodon in his 1738 work Genera piscium, from the report of a beached specimen in the Orkneys in 1693 and two beached in the Netherlands in 1598 and 1601. [28] The 1598 specimen was near Berkhey.[ citation needed ]

The sperm whale is one of the species originally described by Carl Linnaeus in his landmark 1758 10th edition of Systema Naturae. He recognised four species in the genus Physeter. [29] Experts soon realised that just one such species exists, although there has been debate about whether this should be named P. catodon or P. macrocephalus, two of the names used by Linnaeus. Both names are still used, although most recent authors now accept macrocephalus as the valid name, limiting catodon's status to a lesser synonym. Until 1974, the species was generally known as P. catodon. In that year, however, Dutch zoologists Antonius M. Husson and Lipke Holthuis proposed that the correct name should be P. macrocephalus, the second name in the genus Physeter published by Linnaeus concurrently with P. catodon. This proposition was based on the grounds that the names were synonyms published simultaneously, and, therefore, the ICZN Principle of the First Reviser should apply. In this instance, it led to the choice of P. macrocephalus over P. catodon, a view re-stated in Holthuis, 1987. [30] This has been adopted by most subsequent authors, although Schevill (1986 [31] and 1987 [32] ) argued that macrocephalus was published with an inaccurate description and that therefore only the species catodon was valid, rendering the principle of "First Reviser" inapplicable. The most recent version of ITIS has altered its usage from P. catodon to P. macrocephalus, [33] following L. B. Holthuis and more recent (2008) discussions with relevant experts. [34] [35] Furthermore, The Taxonomy Committee of the Society for Marine Mammalogy, the largest international association of marine mammal scientists in the world, officially uses Physeter macrocephalus when publishing their definitive list of marine mammal species. [36]

Biology

External appearance

Average sizes [10] [37]
LengthWeight
Male16 metres (52 ft)45 tonnes (50 short tons)
Female11 metres (36 ft)15 tonnes (17 short tons)
Newborn4 metres (13 ft)1 tonne (1.1 short tons)

The sperm whale is the largest toothed whale and is among the most sexually dimorphic of all cetaceans. [38] Both sexes are about the same size at birth, [10] but mature males are typically 30% to 50% longer and three times as massive as females. [39] [40]

Newborn sperm whales are usually between 3.7 and 4.3 meters (12 and 14 ft) long. [41] Female sperm whales are sexually mature at 8 to 9 meters (26 to 30 ft) in length, whilst males are sexually mature at 11 to 12 meters (36 to 39 ft). [42] Female sperm whales are physically mature at about 10.6 to 11 meters (35 to 36 ft) in length and generally do not achieve lengths greater than 12 metres (39 ft). [38] [40] [42] The largest female sperm whale measured up to 12.3 meters (40 ft) long, and an individual of such size would have weighed about 17 tonnes (19 short tons). [43] [44] Male sperm whales are physically mature at about 15 to 16 meters (49 to 52 ft) in length, and larger males can generally achieve 18 to 19 meters (59 to 62 ft). [42] [45] [38] An 18 meters (59 ft) long male sperm whale is estimated to have weighed 57 tonnes (56 long tons; 63 short tons). [37] By contrast, the second largest toothed whale (Baird's beaked whale) measures up to 12.8 meters (42 ft) and weighs up to 14 tonnes (15 short tons). [46]

There are occasional reports of individual sperm whales achieving even greater lengths, with some historical claims reaching or exceeding 80 feet (24 m). One example is the whale that sank the Essex (one of the incidents behind Moby-Dick ), which was claimed to be 85 feet (26 m). However, there is disagreement as to the accuracy of some of these claims, which are often considered exaggerations or as being measured along the curves of the body. [47] [38] [45]

An individual measuring 20.7 metres (68 ft) was reported from a Soviet whaling fleet near the Kuril Islands in 1950 and is cited by some authors as the largest accurately measured. [38] [48] It has been estimated to weigh 80 tonnes (79 long tons; 88 short tons). [47] In a review of size variation in marine megafauna, McClain and colleagues noted that the International Whaling Commission's data contained eight individuals larger than 20.7 metres (68 ft). The authors supported a 24-metre (79 ft) male from the South Pacific in 1933 as the largest recorded. However, sizes like these are rare, with 95% of recorded sperm whales below 15.85 metres (52.0 ft). [38]

In 1853, one sperm whale was reported at 62 feet (19 m) in length, with a head measuring 20 feet (6.1 m). [49] Large lower jawbones are held in the British Natural History Museum and the Oxford University Museum of Natural History, measuring 5 metres (16 ft) and 4.7 metres (15 ft), respectively. [47]

The average size of sperm whales has decreased over the years, probably due to pressure from whaling. [38] Another view holds that exploitation by overwhaling had virtually no effect on the size of the bull sperm whales, and their size may have actually increased in current times on the basis of density dependent effects. [50] Old males taken at Solander Islands were recorded to be extremely large and unusually rich in blubbers. [51]

Unusual among cetaceans, the sperm whale's blowhole is highly skewed to the left side of the head. Sperm whale blowhole Vincze.jpg
Unusual among cetaceans, the sperm whale's blowhole is highly skewed to the left side of the head.

The sperm whale's unique body is unlikely to be confused with any other species. The sperm whale's distinctive shape comes from its very large, block-shaped head, which can be one-quarter to one-third of the animal's length. The S-shaped blowhole is located very close to the front of the head and shifted to the whale's left. [39] This gives rise to a distinctive bushy, forward-angled spray.[ citation needed ]

The sperm whale's flukes (tail lobes) are triangular and very thick. Proportionally, they are larger than that of any other cetacean, and are very flexible. [52] The whale lifts its flukes high out of the water as it begins a feeding dive. [39] It has a series of ridges on the back's caudal third instead of a dorsal fin. The largest ridge was called the 'hump' by whalers, and can be mistaken for a dorsal fin because of its shape and size. [10]

In contrast to the smooth skin of most large whales, its back skin is usually wrinkly and has been likened to a prune by whale-watching enthusiasts. [53] Albinos have been reported. [11] [54]

Skeleton

A sperm whale skeleton Physeter macrocephalus - skeleton.jpg
A sperm whale skeleton

The ribs are bound to the spine by flexible cartilage, which allows the ribcage to collapse rather than snap under high pressure. [55] While sperm whales are well adapted to diving, repeated dives to great depths have long-term effects. Bones show the same avascular necrosis that signals decompression sickness in humans. Older skeletons showed the most extensive damage, whereas calves showed no damage. This damage may indicate that sperm whales are susceptible to decompression sickness, and sudden surfacing could be lethal to them. [56]

Like that of all cetaceans, the spine of the sperm whale has reduced zygapophysial joints, of which the remnants are modified and are positioned higher on the vertebral dorsal spinous process, hugging it laterally, to prevent extensive lateral bending and facilitate more dorso-ventral bending. These evolutionary modifications make the spine more flexible but weaker than the spines of terrestrial vertebrates. [57]

Labeled sperm whale skeleton Sperm whale skeleton labelled.jpg
Labeled sperm whale skeleton

Like many cetaceans, the sperm whale has a vestigial pelvis that is not connected to the spine.[ citation needed ]

Like that of other toothed whales, the skull of the sperm whale is asymmetrical so as to aid echolocation. Sound waves that strike the whale from different directions will not be channeled in the same way. [58] Within the basin of the cranium, the openings of the bony narial tubes (from which the nasal passages spring) are skewed towards the left side of the skull.[ citation needed ]

Jaws and teeth

Sperm whale tooth Sperm whale tooth.jpg
Sperm whale tooth
The lower jaw is long and narrow. The teeth fit into sockets along the upper jaw. (lifelike sculpture) Dirk Claesen - Sperm Whale.jpg
The lower jaw is long and narrow. The teeth fit into sockets along the upper jaw. (lifelike sculpture)

The sperm whale's lower jaw is very narrow and underslung. [59] The sperm whale has 18 to 26 teeth on each side of its lower jaw which fit into sockets in the upper jaw. [59] The teeth are cone-shaped and weigh up to 1 kilogram (2.2 lb) each. [60] The teeth are functional, but do not appear to be necessary for capturing or eating squid, as well-fed animals have been found without teeth or even with deformed jaws. One hypothesis is that the teeth are used in aggression between males. [61] Mature males often show scars which seem to be caused by the teeth[ citation needed ]. Rudimentary teeth are also present in the upper jaw, but these rarely emerge into the mouth. [62] Analyzing the teeth is the preferred method for determining a whale's age. Like the age-rings in a tree, the teeth build distinct layers of cementum and dentine as they grow. [63]

Brain

The sperm whale's brain is the largest in the world, five times heavier than a human's. Preserved sperm whale brain.jpg
The sperm whale's brain is the largest in the world, five times heavier than a human's.

The sperm whale brain is the largest known of any modern or extinct animal, weighing on average about 7.8 kilograms (17 lb) [64] [65] (with the smallest known weighing 6.4 kilograms (14 lb) and the largest known weighing 9.2 kilograms (20 lb)), [47] [48] more than five times heavier than a human's, and has a volume of about 8,000 cm3. [66] Although larger brains generally correlate with higher intelligence, it is not the only factor. Elephants and dolphins also have larger brains than humans. [67] The sperm whale has a lower encephalization quotient than many other whale and dolphin species, lower than that of non-human anthropoid apes, and much lower than humans'. [65] [68]

The sperm whale's cerebrum is the largest in all mammalia, both in absolute and relative terms. The olfactory system is reduced, suggesting that the sperm whale has a poor sense of taste and smell. By contrast, the auditory system is enlarged. The pyramidal tract is poorly developed, reflecting the reduction of its limbs. [69]

Biological systems

The sperm whale respiratory system has adapted to cope with drastic pressure changes when diving. The flexible ribcage allows lung collapse, reducing nitrogen intake, and metabolism can decrease to conserve oxygen. [70] [71] Between dives, the sperm whale surfaces to breathe for about eight minutes before diving again. [39] Odontoceti (toothed whales) breathe air at the surface through a single, S-shaped blowhole, which is extremely skewed to the left. Sperm whales spout (breathe) 3–5 times per minute at rest, increasing to 6–7 times per minute after a dive. The blow is a noisy, single stream that rises up to 2 metres (6.6 ft) or more above the surface and points forward and left at a 45° angle. [72] On average, females and juveniles blow every 12.5 seconds before dives, while large males blow every 17.5 seconds before dives. [73] A sperm whale killed 160 km (100 mi) south of Durban, South Africa, after a 1-hour, 50-minute dive was found with two dogfish (Scymnodon sp.), usually found at the sea floor, in its belly. [74]

The sperm whale has the longest intestinal system in the world, [75] exceeding 300 m in larger specimens. [76] [77] The sperm whale has a four-chambered stomach that is similar to ruminants. The first secretes no gastric juices and has very thick muscular walls to crush the food (since whales cannot chew) and resist the claw and sucker attacks of swallowed squid. The second chamber is larger and is where digestion takes place. Undigested squid beaks accumulate in the second chamber – as many as 18,000 have been found in some dissected specimens. [76] [78] [79] Most squid beaks are vomited by the whale, but some occasionally make it to the hindgut. Such beaks precipitate the formation of ambergris. [79]

The arterial system of a sperm whale foetus Sperm whale fetus arterial system.svg
The arterial system of a sperm whale foetus

In 1959, the heart of a 22 metric-ton (24 short-ton) male taken by whalers was measured to be 116 kilograms (256 lb), about 0.5% of its total mass. [80] The circulatory system has a number of specific adaptations for the aquatic environment. The diameter of the aortic arch increases as it leaves the heart. This bulbous expansion acts as a windkessel, ensuring a steady blood flow as the heart rate slows during diving. [81] The arteries that leave the aortic arch are positioned symmetrically. There is no costocervical artery. There is no direct connection between the internal carotid artery and the vessels of the brain. [82] Their circulatory system has adapted to dive at great depths, as much as 2,250 metres (7,382 ft) [6] [7] [83] [84] [85] [ excessive citations ] for up to 120 minutes. [86] More typical dives are around 400 metres (1,310 ft) and 35 minutes in duration. [39] Myoglobin, which stores oxygen in muscle tissue, is much more abundant than in terrestrial animals. [87] The blood has a high density of red blood cells, which contain oxygen-carrying haemoglobin. The oxygenated blood can be directed towards only the brain and other essential organs when oxygen levels deplete. [88] [89] [90] The spermaceti organ may also play a role by adjusting buoyancy (see below). [91] The arterial retia mirabilia are extraordinarily well-developed. The complex arterial retia mirabilia of the sperm whale are more extensive and larger than those of any other cetacean. [82]

Senses

Spermaceti organ and melon

Anatomy of the sperm whale's head. The organs above the jaw are devoted to sound generation. Sperm whale head anatomy (transverse + sagittal).svg
Anatomy of the sperm whale's head. The organs above the jaw are devoted to sound generation.

Atop the whale's skull is positioned a large complex of organs filled with a liquid mixture of fats and waxes called spermaceti. The purpose of this complex is to generate powerful and focused clicking sounds, the existence of which was proven by Valentine Worthington and William Schevill when a recording was produced on a research vessel in May 1959. [92] The sperm whale uses these sounds for echolocation and communication. [93] [94] [95] [96] [97] [98] [99] [100] [ excessive citations ]

The spermaceti organ is like a large barrel of spermaceti. Its surrounding wall, known as the case, is extremely tough and fibrous. The case can hold within it up to 1,900 litres of spermaceti. [101] It is proportionately larger in males. [102] This oil is a mixture of triglycerides and wax esters. The proportion of wax esters in the spermaceti organ increases with the age of the whale: 38–51% in calves, 58–87% in adult females, and 71–94% in adult males. [103] The spermaceti at the core of the organ has a higher wax content than the outer areas. [104] The speed of sound in spermaceti is 2,684 m/s (at 40 kHz, 36 °C), making it nearly twice as fast as in the oil in a dolphin's melon. [105]

Below the spermaceti organ lies the "junk" which consists of compartments of spermaceti separated by cartilage. It is analogous to the melon found in other toothed whales. [106] The structure of the junk redistributes physical stress across the skull and may have evolved to protect the head during ramming. [107] [108] [106]

Running through the head are two air passages. The left passage runs alongside the spermaceti organ and goes directly to the blowhole, whilst the right passage runs underneath the spermaceti organ and passes air through a pair of phonic lips and into the distal sac at the very front of the nose. The distal sac is connected to the blowhole and the terminus of the left passage. When the whale is submerged, it can close the blowhole, and air that passes through the phonic lips can circulate back to the lungs. The sperm whale, unlike other odontocetes, has only one pair of phonic lips, whereas all other toothed whales have two, [109] and it is located at the front of the nose instead of behind the melon.

At the posterior end of this spermaceti complex is the frontal sac, which covers the concave surface of the cranium. The posterior wall of the frontal sac is covered with fluid-filled knobs, which are about 4–13 mm in diameter and separated by narrow grooves. The anterior wall is smooth. The knobbly surface reflects sound waves that come through the spermaceti organ from the phonic lips. The grooves between the knobs trap a film of air that is consistent whatever the orientation or depth of the whale, making it an excellent sound mirror. [105]

The spermaceti organs may also help adjust the whale's buoyancy. It is hypothesized that before the whale dives, cold water enters the organ, and it is likely that the blood vessels constrict, reducing blood flow, and, hence, temperature. The wax therefore solidifies and reduces in volume. [91] [110] The increase in specific density generates a down force of about 392 newtons (88 lbf) and allows the whale to dive with less effort.[ citation needed ] During the hunt, oxygen consumption, together with blood vessel dilation, produces heat and melts the spermaceti, increasing its buoyancy and enabling easy surfacing. [111] However, more recent work [95] has found many problems with this theory including the lack of anatomical structures for the actual heat exchange. [112] Another issue is that if the spermaceti does indeed cool and solidify, it would affect the whale's echolocation ability just when it needs it to hunt in the depths.[ citation needed ]

Herman Melville's fictional story Moby-Dick suggests that the "case" containing the spermaceti serves as a battering ram for use in fights between males. [113] A few famous instances include the well-documented sinking of the ships Essex and Ann Alexander by attackers estimated to weigh only one-fifth as much as the ships. [106]

Eyes and vision

Like other toothed whales, the sperm whale can retract its eyes.

The sperm whale's eye does not differ greatly from those of other toothed whales except in size. It is the largest among the toothed whales, weighing about 170 g. It is overall ellipsoid in shape, compressed along the visual axis, measuring about 7×7×3 cm. The cornea is elliptical and the lens is spherical. The sclera is very hard and thick, roughly 1 cm anteriorly and 3 cm posteriorly. There are no ciliary muscles. The choroid is very thick and contains a fibrous tapetum lucidum . Like other toothed whales, the sperm whale can retract and protrude its eyes, thanks to a 2-cm-thick retractor muscle attached around the eye at the equator, [114] but are unable to roll the eyes in their sockets. [115]

According to Fristrup and Harbison (2002), [116] sperm whale's eyes afford good vision and sensitivity to light. They conjectured that sperm whales use vision to hunt squid, either by detecting silhouettes from below or by detecting bioluminescence. If sperm whales detect silhouettes, Fristrup and Harbison suggested that they hunt upside down, allowing them to use the forward parts of the ventral visual fields for binocular vision.[ citation needed ]

Sleeping

For some time researchers have been aware that pods of sperm whales may sleep for short periods, assuming a vertical position with their heads just below or at the surface, or head down. [117] A 2008 study published in Current Biology recorded evidence that whales may sleep with both sides of the brain. It appears that some whales may fall into a deep sleep for about 7 percent of the time, most often between 6 p.m. and midnight. [118]

Genetics

Sperm whales have 21 pairs of chromosomes (2n=42). [119] The genome of live whales can be examined by recovering shed skin. [120]

Vocalization complex

Sperm whale vocalization

After Valentine Worthington and William E. Schevill confirmed the existence of sperm whale vocalization, [92] further studies found that sperm whales are capable of emitting sounds at a volume of 230 decibels   more than an aircraft jet engine at takeoff  making the sperm whale the loudest animal in the world. [121]

Mechanism

When echolocating, the sperm whale emits a directionally focused beam of broadband clicks. Clicks are generated by forcing air through a pair of phonic lips (also known as "monkey lips" or "museau de singe") at the front end of the nose, just below the blowhole. The sound then travels backwards along the length of the nose through the spermaceti organ. Most of the sound energy is then reflected off the frontal sac at the cranium and into the melon, whose lens-like structure focuses it. [93] Some of the sound will reflect back into the spermaceti organ and back towards the front of the whale's nose, where it will be reflected through the spermaceti organ a third time. This back and forth reflection which happens on the scale of a few milliseconds creates a multi-pulse click structure. [122] This multi-pulse click structure allows researchers to measure the whale's spermaceti organ using only the sound of its clicks. [123] [124] Because the interval between pulses of a sperm whale's click is related to the length of the sound producing organ, an individual whale's click is unique to that individual. However, if the whale matures and the size of the spermaceti organ increases, the tone of the whale's click will also change. [124] The lower jaw is the primary reception path for the echoes. A continuous fat-filled canal transmits received sounds to the inner ear. [125]

The source of the air forced through the phonic lips is the right nasal passage. While the left nasal passage opens to the blow hole, the right nasal passage has evolved to supply air to the phonic lips. It is thought that the nostrils of the land-based ancestor of the sperm whale migrated through evolution to their current functions, the left nostril becoming the blowhole and the right nostril becoming the phonic lips. [126]

Air that passes through the phonic lips passes into the distal sac, then back down through the left nasal passage. This recycling of air allows the whale to continuously generate clicks for as long as it is submerged. [127]

Types of vocalization

The sperm whale's vocalizations are all based on clicking, described in four types: the usual echolocation, creaks, codas, and slow clicks. [128]

The usual echolocation click type is used in searching for prey. [128] A creak is a rapid series of high-frequency clicks that sounds somewhat like a creaky door hinge. It is typically used when homing in on prey. [128]

Slow clicks are heard only in the presence of males (it is not certain whether females occasionally make them). Males make a lot of slow clicks in breeding grounds (74% of the time), both near the surface and at depth, which suggests they are primarily mating signals. Outside breeding grounds, slow clicks are rarely heard, and usually near the surface. [129]

Characteristics of sperm whale clicks [128]
Click typeApparent
source level
(dB re 1 µPa m)
DirectionalityCentroid
frequency
(kHz)
Inter-click
interval
(s)
Duration
of click
(ms)
Duration
of pulse
(ms)
Range audible
to sperm whale
(km)
Inferred functionAudio sample
Usual230High150.5–1.015–300.116Searching for prey
Creak205High150.005–0.10.1–50.16Homing in on prey
Coda180Low50.1–0.5350.5~2Social communication
Slow190Low0.55–830560Communication by males

Codas

The most distinctive vocalizations are codas, which are short rhythmic sequences of clicks, mostly numbering 3–12 clicks, in stereotyped patterns. [130] They are classified using variations in the number of clicks, rhythm, and tempo. [131]

Codas are the result of vocal learning within a stable social group, [132] and are made in the context of the whales' social unit. [130] “The foundation of sperm whale society is the matrilineally based social unit of ten or so females and their offspring. The members of the unit travel together, suckle each others' infants, and babysit them while mothers make long deep dives to feed.” [130] Over 70% of a sperm whale's time is spent independently foraging; codas “could help whales reunite and reaffirm their social ties in between long foraging dives.” [131] [133]

While nonidentity codas are commonly used in multiple different clans, [134] some codas express clan identity, and denote different patterns of travel, foraging, and socializing or avoidance among clans. [133] [135] In particular, whales will not group with whales of another clan even though they share the same geographical area. [130] Statistically, as the clans' ranges become more overlapped, the distinction in clan identity coda usage becomes more pronounced. [134] Distinctive codas identify seven clans described among the approximately 150,000 female sperm whales in the Pacific Ocean, and there are another four clans in the Atlantic. [130] As “arbitrary traits that function as reliable indicators of cultural group membership,” clan identity codas act as symbolic markers that modulate interactions between individuals. [131]

Individual identity in sperm whale vocalizations is an ongoing scientific issue, however. A distinction needs to be made between cues and signals. Human acoustic tools can distinguish individual whales by analyzing micro-characteristics of their vocalizations, [136] and the whales can probably do the same. This does not prove that the whales deliberately use some vocalizations to signal individual identity in the manner of the signature whistles that bottlenose dolphins use as individual labels. [132] [131]

Ecology

Distribution

Global concentrations of sperm whales Sperm whale distribution (Pacific equirectangular).jpg
Global concentrations of sperm whales

Sperm whales are among the most cosmopolitan species. They prefer ice-free waters over 1,000 metres (3,300 ft) deep. [3] Although both sexes range through temperate and tropical oceans and seas, only adult males populate higher latitudes. [11] Among several regions, such as along coastal waters of southern Australia, sperm whales have been considered to be locally extinct. [137]

They are relatively abundant from the poles to the equator and are found in all the oceans. They inhabit the Mediterranean Sea, but not the Black Sea, [10] while their presence in the Red Sea is uncertain. [3] The shallow entrances to both the Black Sea and the Red Sea may account for their absence. [138] The Black Sea's lower layers are also anoxic and contain high concentrations of sulphur compounds such as hydrogen sulphide. [139] [ What does being anoxic have to do with whales that don't breath under water? Lack of prey? ] The first ever sighting off the coast of Pakistan was made in 2017. [140] [141] The first ever record off the west coast of the Korean Peninsula (Yellow Sea) was made in 2005. [142] [143] followed by one near Ganghwa Island in 2009. [144]

Populations are denser close to continental shelves and canyons. [11] Sperm whales are usually found in deep, off-shore waters, but may be seen closer to shore, in areas where the continental shelf is small and drops quickly to depths of 310 to 920 metres (1,020 to 3,020 ft). [10] Coastal areas with significant sperm whale populations include the Azores and Dominica. [145] In east Asian waters, whales are also observed regularly in coastal waters in places such as the Commander and Kuril Islands, Shiretoko Peninsula which is one of few locations where sperm whales can be observed from shores, [146] off Kinkasan, vicinity to Tokyo Bay [147] and the Bōsō Peninsula to the Izu [148] [149] and the Izu Islands, the Volcano Islands, Yakushima and the Tokara Islands to the Ryukyu Islands, [150] [151] Taiwan, the Northern Mariana Islands, [152] and so forth. Historical catch records suggest there could have been smaller aggression grounds in the Sea of Japan as well. [153] Along the Korean Peninsula, the first confirmed observation within the Sea of Japan, eight animals off Guryongpo, was made in 2004 since after the last catches of five whales off Ulsan in 1911, [143] [154] while nine whales were observed in the East China Sea side of the peninsula in 1999. [155]

Grown males are known to enter surprisingly shallow bays to rest (whales will be in a state of rest during these occasions). Unique, coastal groups have been reported from various areas around the globe, such as near Scotland's coastal waters, [156] and the Shiretoko Peninsula, off Kaikōura, in Davao Gulf. Such coastal groups were more abundant in pre-whaling days. [157]

Genetic analysis indicates that the world population of sperm whales originated in the Pacific Ocean from a population of about 10,000 animals around 100,000 years ago, when expanding ice caps blocked off their access to other seas. In particular, colonization of the Atlantic was revealed to have occurred multiple times during this expansion of their range. [158]

Diet

A piece of sperm whale skin with giant squid sucker scars A piece of sperm whale skin with Giant Squid sucker scars.JPG
A piece of sperm whale skin with giant squid sucker scars

Sperm whales usually dive between 300 and 800 metres (980 and 2,620 ft), and sometimes 1 to 2 kilometres (3,300 to 6,600 ft), in search of food. [159] Such dives can last more than an hour. [159] They feed on several species, notably the giant squid, but also the colossal squid, octopuses, and fish such as demersal rays and sharks,[ citation needed ] but their diet is mainly medium-sized squid. [160] Some prey may be taken accidentally while eating other items. [160] Most of what is known about deep-sea squid has been learned from specimens in captured sperm whale stomachs, although more recent studies analysed faeces. One study, carried out around the Galápagos, found that squid from the genera Histioteuthis (62%), Ancistrocheirus (16%), and Octopoteuthis (7%) weighing between 12 and 650 grams (0.026 and 1.433 lb) were the most commonly taken. [161] Battles between sperm whales and giant squid or colossal squid have never been observed by humans; however, white scars are believed to be caused by the large squid. One study published in 2010 collected evidence that suggests that female sperm whales may collaborate when hunting Humboldt squid. [162] Tagging studies have shown that sperm whales hunt upside down at the bottom of their deep dives. It is suggested that the whales can see the squid silhouetted above them against the dim surface light. [163]

An older study, examining whales captured by the New Zealand whaling fleet in the Cook Strait region, found a 1.69:1 ratio of squid to fish by weight. [164] Sperm whales sometimes take sablefish and toothfish from long lines. Long-line fishing operations in the Gulf of Alaska complain that sperm whales take advantage of their fishing operations to eat desirable species straight off the line, sparing the whales the need to hunt. [165] However, the amount of fish taken is very little compared to what the sperm whale needs per day. Video footage has been captured of a large male sperm whale "bouncing" a long line, to gain the fish. [166] Sperm whales are believed to prey on the megamouth shark, a rare and large deep-sea species discovered in the 1970s. [167] In one case, three sperm whales were observed attacking or playing with a megamouth. [168]

Sperm whales have also been noted to feed on bioluminescent pyrosomes such as Pyrosoma atlanticum . [169] [170] [171] It is thought that the foraging strategy of sperm whales for bioluminescent squids may also explain the presence of these light-emitting pyrosomes in the diet of the sperm whale. [171]

Ambergris Ambergris.jpg
Ambergris

The sharp beak of a consumed squid lodged in the whale's intestine may lead to the production of ambergris, analogous to the production of pearls in oysters. [172] The irritation of the intestines caused by squid beaks stimulates the secretion of this lubricant-like substance. Sperm whales are prodigious feeders and eat around 3% of their body weight per day. The total annual consumption of prey by sperm whales worldwide is estimated to be about 272 million tonnes (300 million short tons). [173] [174] In comparison, human consumption of seafood is estimated to be 157 million tonnes (173 million short tons). [175]

Sperm whales hunt through echolocation. Their clicks are among the most powerful sounds in the animal kingdom (see above). It has been hypothesised that it can stun prey with its clicks. Experimental studies attempting to duplicate this effect have been unable to replicate the supposed injuries, casting doubt on this idea. [176] One study showing that sound pressure levels on the squid are more than an order of magnitude below levels required for debilitation, and therefore, precluding acoustic stunning to facilitate prey capture. [177]

Sperm whales, as well as other large cetaceans, help fertilise the surface of the ocean by consuming nutrients in the depths and transporting those nutrients to the oceans' surface when they defecate, an effect known as the whale pump. [178] This fertilises phytoplankton and other plants on the surface of the ocean and contributes to ocean productivity and the drawdown of atmospheric carbon. [179]

Life cycle

Sperm whales can live 70 years or more. [10] [11] [12] They are a prime example of a species that has been K-selected, meaning their reproductive strategy is associated with stable environmental conditions and comprises a low birth rate, significant parental aid to offspring, slow maturation, and high longevity. [39]

How they choose mates has not been definitively determined. Bulls will fight with each other over females, and males will mate with multiple females, making them polygynous, but they do not dominate the group as in a harem. [180] [181] Bulls do not provide paternal care to their offspring but rather play a fatherly role to younger bulls to show dominance. [182]

Females become fertile at around 9 years of age. [183] The oldest pregnant female ever recorded was 41 years old. [184] Gestation requires 14 to 16 months, producing a single calf. [10] Sexually mature females give birth once every 4 to 20 years (pregnancy rates were higher during the whaling era). [183] Birth is a social event, as the mother and calf need others to protect them from predators. The other adults may jostle and bite the newborn in its first hours. [185]

Lactation proceeds for 19 to 42 months, but calves, rarely, may suckle up to 13 years. [10] Like that of other whales, the sperm whale's milk has a higher fat content than that of terrestrial mammals: about 36%, [186] compared to 4% in cow milk. This gives it a consistency similar to cottage cheese, [187] which prevents it from dissolving in the water before the calf can drink it. [188] It has an energy content of roughly 3,840 kcal/kg, [186] compared to just 640 kcal/kg in cow milk. [189] Calves may be allowed to suckle from females other than their mothers. [10]

Males become sexually mature at 18 years. Upon reaching sexual maturity, males move to higher latitudes, where the water is colder and feeding is more productive. Females remain at lower latitudes. [10] Males reach their full size at about age 50. [39]

Social behaviour

Relations within the species

Sperm whales adopt the "marguerite formation" to defend a vulnerable pod member. Marguerite formation Vector.svg
Sperm whales adopt the "marguerite formation" to defend a vulnerable pod member.

Like elephants, females and their young live in matriarchal groups called pods, while bulls live apart. Bulls sometimes form loose bachelor groups with other males of similar age and size. As they grow older, they typically live solitary lives, only returning to the pod to socialize or to breed. [39] Bulls have beached themselves together, suggesting a degree of cooperation which is not yet fully understood. [39] The whales rarely, if ever, leave their group. [190]

A social unit is a group of sperm whales who live and travel together over a period of years. Individuals rarely, if ever, join or leave a social unit. There is a huge variance in the size of social units. They are most commonly between six and nine individuals in size but can have more than twenty. [191] Unlike orcas, sperm whales within a social unit show no significant tendency to associate with their genetic relatives. [192] Females and calves spend about three-quarters of their time foraging and a quarter of their time socializing. Socializing usually takes place in the afternoon. [193]

When sperm whales socialize, they emit complex patterns of clicks called codas. They will spend much of the time rubbing against each other. Tracking of diving whales suggests that groups engage in herding of prey, similar to bait balls created by other species, though the research needs to be confirmed by tracking the prey. [194] [195]

Relations with other species

The most common natural predator of sperm whales is the orca (killer whale), but pilot whales and false killer whales sometimes harass them. [196] [197] Orcas prey on target groups of females with young, usually making an effort to extract and kill a calf. The females will protect their calves or an injured adult by encircling them. They may face inwards with their tails out (the 'marguerite formation', named after the flower). The heavy and powerful tail of an adult whale is potentially capable of delivering lethal blows. [198] Alternatively, they may face outwards (the 'heads-out formation'). Other than sperm whales, southern right whales had been observed to perform similar formations. [199] However, formations in non-dangerous situations have been recorded as well. [199] Early whalers exploited this behaviour, attracting a whole unit by injuring one of its members. [200] Such a tactic is described in Moby-Dick :

"Say you strike a Forty-barrel-bull—poor devil! all his comrades quit him. But strike a member of the harem school, and her companions swim around her with every token of concern, sometimes lingering so near her and so long, as themselves to fall a prey." [201]

If the killer whale pod is large, its members may sometimes be able to kill adult female sperm whales and can at least injure an entire pod of sperm whales. [202] [203] Bulls have no predators, and are believed to be too large, powerful and aggressive to be threatened by killer whales. [204] Solitary bulls are known to interfere and come to the aid of vulnerable groups nearby. [205] However, the bull sperm whale, when accompanying pods of female sperm whales and their calves as such, may be reportedly unable to effectively dissuade killer whales from their attacks on the group, although the killer whales may end the attack sooner when a bull is present. [206] [207] However, male sperm whales have been observed to attack and intimidate killer whale pods in competitive feeding instances. An incident was filmed from a long-line trawler: a killer whale pod was systematically taking fish caught on the trawler's long lines (as the lines were being pulled into the ship) when a male sperm whale appeared to repeatedly charge the killer whale pod in an attempt to drive them away; it was speculated by the film crew that the sperm whale was attempting to access the same fish. The killer whales employed a tail outward and tail-slapping defensive position against the bull sperm whale similar to that used by female sperm whales against attacking killer whales. [208] However, at some potential feeding sites, the killer whales may prevail over sperm whales even when outnumbered by the sperm whales. Some authors consider the killer whales "usually" behaviorally dominant over sperm whales but express that the two species are "fairly evenly matched", with the killer whales' greater aggression, more considerable biting force for their size and predatory prowess more than compensating for their smaller size. [206] [209]

Sperm whales are not known for forging bonds with other species, but it was observed that a bottlenose dolphin with a spinal deformity had been accepted into a pod of sperm whales. [210] They are known to swim alongside other cetaceans such as humpback, [211] fin, minke, pilot, [212] and killer whales on occasion. [213]

Parasites

Sperm whales can suffer from parasites. Out of 35 sperm whales caught during the 1976–1977 Antarctic whaling season, all of them were infected by Anisakis physeteris (in their stomachs) and Phyllobothrium delphini (in their blubber). Both whales with a placenta were infected with Placentonema gigantissima , [214] potentially the largest nematode worm ever described.[ citation needed ]

Evolutionary history

Cetacea     
Toothed whales
Physeteroidea

Other Physeteroidea

Kogiidae

Pygmy sperm whale

Dwarf sperm whale

Physeteridae

Other Physeteridae

Sperm whale

South Asian river dolphin

Other river dolphins

Oceanic dolphins

Porpoises

Arctic whales

Beaked whales

Baleen whales

Evolutionary family tree of sperm whales, [215]
including simplified summary of extinct groups () [216]

Fossil record

Although the fossil record is poor, [217] several extinct genera have been assigned to the clade Physeteroidea, which includes the last common ancestor of the modern sperm whale, pygmy sperm whales, dwarf sperm whales, and extinct physeteroids. These fossils include Ferecetotherium , Idiorophus , Diaphorocetus , Aulophyseter , Orycterocetus , Scaldicetus , Placoziphius , Zygophyseter and Acrophyseter . [27] [216] [218] Ferecetotherium, found in Azerbaijan and dated to the late Oligocene (about 28 to 23 million years ago), is the most primitive fossil that has been found, which possesses sperm whale-specific features, such as an asymmetric rostrum ("beak" or "snout"). [219] Most sperm whale fossils date from the Miocene period, 23 to 5 million years ago. Diaphorocetus, from Argentina, has been dated to the early Miocene. Fossil sperm whales from the Middle Miocene include Aulophyseter, Idiorophus and Orycterocetus, all of which were found on the West Coast of the United States, and Scaldicetus, found in Europe and Japan. [219] [220] Orycterocetus fossils have also been found in the North Atlantic Ocean and the Mediterranean Sea, in addition to the west coast of the United States. [221] Placoziphius, found in Europe, and Acrophyseter, from Peru, are dated to the late Miocene. [27] [219]

Fossil sperm whales differ from modern sperm whales in tooth count and the shape of the face and jaws. [219] For example, Scaldicetus had a tapered rostrum. [220] Genera from the Oligocene and early and middle Miocene, with the possible exception of Aulophyseter, had teeth in their upper jaws. [219] Acrophyseter, from the late Miocene, also had teeth in both the upper and lower jaws as well as a short rostrum and an upward curving mandible (lower jaw). [27] These anatomical differences suggest that fossil species may not have necessarily been deep-sea squid eaters such as the modern sperm whale, but that some genera mainly ate fish. [219] Zygophyseter, dated from the middle to late Miocene and found in southern Italy, had teeth in both jaws and appears to have been adapted to feed on large prey, rather like the modern killer whale (orca). Other fossil sperm whales with adaptations similar to this are collectively known as killer sperm whales. [216]

Two poorly known fossil species belonging to the modern genus Physeter have been recognized so far: P. antiquus (Neogene of France) [222] and P. vetus (Neogene of eastern North America). [223] Physeter vetus is very likely an invalid species, as the few teeth that were used to identify this species appear to be identical to those of another toothed whale, Orycterocetus quadratidens . [224]

Phylogeny

The traditional view has been that Mysticeti (baleen whales) and Odontoceti (toothed whales) arose from more primitive whales early in the Oligocene period, and that the super-family Physeteroidea, which contains the sperm whale, dwarf sperm whale, and pygmy sperm whale, diverged from other toothed whales soon after that, over 23  million years ago. [217] [219] From 1993 to 1996, molecular phylogenetics analyses by Milinkovitch and colleagues, based on comparing the genes of various modern whales, suggested that the sperm whales are more closely related to the baleen whales than they are to other toothed whales, which would have meant that Odontoceti were not monophyletic; in other words, it did not consist of a single ancestral toothed whale species and all its descendants. [215] However, more recent studies, based on various combinations of comparative anatomy and molecular phylogenetics, criticised Milinkovitch's analysis on technical grounds and reaffirmed that the Odontoceti are monophyletic. [215] [225] [226]

These analyses also confirm that there was a rapid evolutionary radiation (diversification) of the Physeteroidea in the Miocene period. [216] The Kogiidae (dwarf and pygmy sperm whales) diverged from the Physeteridae (true sperm whales) at least 8  million years ago. [225]

Relationship with humans

Sperm whaling

In the 19th century, sperm whales were hunted using rowboats and hand-thrown harpoons, a rather dangerous method, as the whales sometimes fought back. Whaling of sperm whale.jpg
In the 19th century, sperm whales were hunted using rowboats and hand-thrown harpoons, a rather dangerous method, as the whales sometimes fought back.

Spermaceti, obtained primarily from the spermaceti organ, and sperm oil, obtained primarily from the blubber in the body, were much sought after by 18th, 19th, and 20th century whalers. These substances found a variety of commercial applications, such as candles, soap, cosmetics, machine oil, other specialised lubricants, lamp oil, pencils, crayons, leather waterproofing, rust-proofing materials and many pharmaceutical compounds. [227] [228] [229] [230] Ambergris, a highly expensive, solid, waxy, flammable substance produced in the digestive system of sperm whales, was also sought as a fixative in perfumery.[ citation needed ]

Prior to the early eighteenth century, hunting was mostly by indigenous Indonesians. [231] Legend has it that sometime in the early 18th century, around 1712, Captain Christopher Hussey, while cruising for right whales near shore, was blown offshore by a northerly wind, where he encountered a sperm whale pod and killed one. [232] Although the story may not be true, sperm whales were indeed soon exploited by American whalers. Judge Paul Dudley, in his Essay upon the Natural History of Whales (1725), states that a certain Atkins, 10 or 12 years in the trade, was among the first to catch sperm whales sometime around 1720 off the New England coast. [233]

There were only a few recorded instances during the first few decades (1709–1730s) of offshore sperm whaling. Instead, sloops concentrated on the Nantucket Shoals, where they would have taken right whales or went to the Davis Strait region to catch bowhead whales. By the early 1740s, with the advent of spermaceti candles (before 1743), American vessels began to focus on sperm whales. The diary of Benjamin Bangs (1721–1769) shows that, along with the bumpkin sloop he sailed, he found three other sloops flensing sperm whales off the coast of North Carolina in late May 1743. [234] On returning to Nantucket in the summer 1744 on a subsequent voyage, he noted that "45 spermacetes are brought in here this day," another indication that American sperm whaling was in full swing. [234]

American sperm whaling soon spread from the east coast of the American colonies to the Gulf Stream, the Grand Banks, West Africa (1763), the Azores (1765), and the South Atlantic (1770s). From 1770 to 1775 Massachusetts, New York, Connecticut, and Rhode Island ports produced 45,000 barrels of sperm oil annually, compared to 8,500 of whale oil. [235] In the same decade, the British began sperm whaling, employing American ships and personnel. [236] By the following decade, the French had entered the trade, also employing American expertise. [236] Sperm whaling increased until the mid-nineteenth century. Spermaceti oil was important in public lighting (for example, in lighthouses, where it was used in the United States until 1862, when it was replaced by lard oil, in turn replaced by petroleum) and for lubricating the machines (such as those used in cotton mills) of the Industrial Revolution. Sperm whaling declined in the second half of the nineteenth century, as petroleum came into broader use. In that sense, petroleum use may be said to have protected whale populations from even greater exploitation. [237] [238] Sperm whaling in the 18th century began with small sloops carrying only one or two whaleboats. The fleet's scope and size increased over time, and larger ships entered the fishery. In the late 18th century and early 19th century, sperm whaling ships sailed to the equatorial Pacific, the Indian Ocean, Japan, the coast of Arabia, Australia and New Zealand. [236] [239] [240] Hunting could be dangerous to the crew, since sperm whales (especially bulls) will readily fight to defend themselves against attack, unlike most baleen whales. When dealing with a threat, sperm whales will use their huge head effectively as a battering ram. [106] Arguably the most famous sperm whale counter-attack occurred on 20 November 1820, when a whale claimed to be about 25.9 metres (85 ft) long rammed and sank the Nantucket whaleship Essex . Only 8 out of 21 sailors survived to be rescued by other ships. [241]

Scrimshaw was the art of engraving on the teeth of sperm whales. It was a way for whalers to pass the time between hunts. Nantucket Whaling scrimshaw E.Burdett.jpg
Scrimshaw was the art of engraving on the teeth of sperm whales. It was a way for whalers to pass the time between hunts.

The sperm whale's ivory-like teeth were often sought by 18th- and 19th-century whalers, who used them to produce inked carvings known as scrimshaw. 30 teeth of the sperm whale can be used for ivory. Each of these teeth, up to 20 cm (8 in) and 8 cm (3 in) across, are hollow for the first half of their length. Like walrus ivory, sperm whale ivory has two distinct layers. However, sperm whale ivory contains a much thicker inner layer. Though a widely practised art in the 19th century, scrimshaw using genuine sperm whale ivory declined substantially after the retirement of the whaling fleets in the 1880s.[ citation needed ]

Modern whaling was more efficient than open-boat whaling, employing steam-powered ships and exploding harpoons. Initially, modern whaling activity focused on large baleen whales, but as these populations were taken, sperm whaling increased. Spermaceti, the fine waxy oil produced by sperm whales, was in high demand. In both the 1941–1942 and 1942–1943 seasons, Norwegian expeditions took over 3,000 sperm whales off the coast of Peru alone. After World War II, whaling continued unabated to obtain oil for cosmetics and high-performance machinery, such as automobile transmissions.[ citation needed ]

The hunting led to the near-extinction of large whales, including sperm whales, until bans on whale oil use were instituted in 1972. The International Whaling Commission gave the species full protection in 1985, but hunting by Japan in the northern Pacific Ocean continued until 1988. [238]

It is estimated that the historic worldwide population numbered 1,100,000 before commercial sperm whaling began in the early 18th century. [3] By 1880, it had declined by an estimated 29 percent. [3] From that date until 1946, the population appears to have partially recovered as whaling activity decreased, but after the Second World War, the population declined even further, to 33 per cent of the pre-whaling population.[ citation needed ] Between 184,000 and 236,000 sperm whales were killed by the various whaling nations in the 19th century, [242] while in the 20th century, at least 770,000 were taken, the majority between 1946 and 1980. [243]

Sperm whaling peaked in the 1830s and 1960s. Sperm whale catches.jpg
Sperm whaling peaked in the 1830s and 1960s.

Sperm whales increase levels of primary production and carbon export by depositing iron-rich faeces into surface waters of the Southern Ocean. The iron-rich faeces cause phytoplankton to grow and take up more carbon from the atmosphere. When the phytoplankton dies, it sinks to the deep ocean and takes the atmospheric carbon with it. By reducing the abundance of sperm whales in the Southern Ocean, whaling has resulted in an extra 2 million tonnes of carbon remaining in the atmosphere each year. [244]

Remaining sperm whale populations are large enough that the species' conservation status is rated as vulnerable rather than endangered. [3] However, the recovery from centuries of commercial whaling is a slow process, particularly in the South Pacific, where the toll on breeding-age males was severe. [245]

Current conservation status

The total number of sperm whales in the world is unknown, but is thought to be in the hundreds of thousands. [3] The conservation outlook is brighter than for many other whales. Commercial whaling has ceased, [3] and the species is protected almost worldwide, though records indicate that in the 11-year period starting from 2000, Japanese vessels have caught 51 sperm whales.[ needs update ] Fishermen do not target sperm whales to eat, [3] but long-line fishing operations in the Gulf of Alaska have complained about sperm whales stealing fish from their lines. [165]

Currently, entanglement in fishing nets and collisions with ships represent the greatest threats to the sperm whale population. [11] Other threats include ingestion of marine debris, ocean noise, and chemical pollution. [246] The International Union for Conservation of Nature (IUCN) regards the sperm whale as being "vulnerable". [3] The species is listed as endangered on the United States Endangered Species Act. [247]

Sperm whales are listed on Appendix I [248] and Appendix II [248] of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). It is listed on Appendix I [248] as this species has been categorized as being in danger of extinction throughout all or a significant proportion of their range and CMS Parties strive towards strictly protecting these animals, conserving or restoring the places where they live, mitigating obstacles to migration and controlling other factors that might endanger them. It is listed on Appendix II [248] as it has an unfavourable conservation status or would benefit significantly from international co-operation organised by tailored agreements. It is also covered by the Agreement on the Conservation of Cetaceans in the Black Sea, Mediterranean Sea and Contiguous Atlantic Area (ACCOBAMS) and the Memorandum of Understanding for the Conservation of Cetaceans and Their Habitats in the Pacific Islands Region (Pacific Cetaceans MOU).[ citation needed ]

The species is protected under Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). This makes commercial international trade (including in parts and derivatives) prohibited, with all other international trade strictly regulated through a system of permits and certificates. [4]

Cultural importance

Sperm whale teeth necklace from Fiji Necklace, sperm whale teeth, Fiji, c 1895 - Staatlichen Museums fur Volkerkunde Munchen - DSC08280.JPG
Sperm whale teeth necklace from Fiji

Rope-mounted teeth are important cultural objects throughout the Pacific. In New Zealand, the Māori know them as "rei puta"; such whale tooth pendants were rare objects because sperm whales were not actively hunted in traditional Māori society. [249] Whale ivory and bone were taken from beached whales. In Fiji the teeth are known as tabua , traditionally given as gifts for atonement or esteem (called sevusevu), and were important in negotiations between rival chiefs. [250] Friedrich Ratzel in The History of Mankind reported in 1896 that, in Fiji, whales' or cachalots' teeth were the most-demanded article of ornament or value. They occurred often in necklaces. [251] Today the tabua remains an important item in Fijian life. The teeth were originally rare in Fiji and Tonga, which exported teeth, but with the Europeans' arrival, teeth flooded the market and this "currency" collapsed. The oversupply led in turn to the development of the European art of scrimshaw. [252]

Herman Melville's novel Moby-Dick is based on a true story about a sperm whale that attacked and sank the whaleship Essex . [253] [254] Melville associated the sperm whale with the Bible's Leviathan. [254] [255] The fearsome reputation perpetuated by Melville was based on bull whales' ability to fiercely defend themselves from attacks by early whalers, smashing whaling boats and, occasionally, attacking and destroying whaling ships.[ citation needed ]

In Jules Verne's Twenty Thousand Leagues Under the Sea , the Nautilus fights a group of "cachalots" (sperm whales) to protect a pod of southern right whales from their attacks. Verne portrays them as being savage hunters ("nothing but mouth and teeth").[ citation needed ]

The sperm whale was designated as the Connecticut state animal by the General Assembly in 1975. [256] It was selected because of its specific contribution to the state's history and because of its present-day plight as an endangered species. [257]

Watching sperm whales

Sperm whales are not the easiest of whales to watch, due to their long dive times and ability to travel long distances underwater. However, due to the distinctive look and large size of the whale, watching is increasingly popular.[ citation needed ] Sperm whale watchers often use hydrophones to listen to the clicks of the whales and locate them before they surface. [258] Popular locations for sperm whale watching include the town of Kaikōura on New Zealand's South Island, Andenes and Tromsø in Arctic Norway; as well as the Azores, where the continental shelf is so narrow that whales can be observed from the shore, [145] [259] and Dominica [260] where a long-term scientific research program, The Dominica Sperm Whale Project, has been in operation since 2005. [261]

Plastic waste

The introduction of plastic waste to the ocean environment by humans is relatively new. From the 1970s, sperm whales have occasionally been found with pieces of plastic in their stomachs. [171] [262] [263] [264]

See also

Notes

  1. /ˈkæʃəlɒt,ˈkæʃəl/ "cachalot" . Oxford English Dictionary (Online ed.). Oxford University Press.(Subscription or participating institution membership required.)

Related Research Articles

<span class="mw-page-title-main">Cetacea</span> Infraorder of mammals

Cetacea 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.

<span class="mw-page-title-main">Whale</span> Informal group of large marine mammals

Whales are a widely distributed and diverse group of fully aquatic placental marine mammals. As an informal and colloquial grouping, they correspond to large members of the infraorder Cetacea, i.e. all cetaceans apart from dolphins and porpoises. Dolphins and porpoises may be considered whales from a formal, cladistic perspective. Whales, dolphins and porpoises belong to the order Cetartiodactyla, which consists of even-toed ungulates. Their closest non-cetacean living relatives are the hippopotamuses, from which they and other cetaceans diverged about 54 million years ago. The two parvorders of whales, baleen whales (Mysticeti) and toothed whales (Odontoceti), are thought to have had their last common ancestor around 34 million years ago. Mysticetes include four extant (living) families: Balaenopteridae, Balaenidae, Cetotheriidae, and Eschrichtiidae. Odontocetes include the Monodontidae, Physeteridae, Kogiidae, and Ziphiidae, as well as the six families of dolphins and porpoises which are not considered whales in the informal sense.

<span class="mw-page-title-main">Spermaceti</span> Waxy substance found in the head cavities of sperm whales

Spermaceti is a waxy substance found in the head cavities of the sperm whale. Spermaceti is created in the spermaceti organ inside the whale's head. This organ may contain as much as 1,900 litres (500 US gal) of spermaceti. It has been extracted by whalers since the 17th century for human use in cosmetics, textiles, and candles.

<span class="mw-page-title-main">Physeteroidea</span> Superfamily of toothed whales

Physeteroidea is a superfamily that includes three extant species of whales: the sperm whale, in the genus Physeter, and the pygmy sperm whale and dwarf sperm whale, in the genus Kogia. In the past, these genera have sometimes been united in a single family, the Physeteridae, with the two Kogia species in the subfamily Kogiinae; however, recent practice is to allocate the genus Kogia to its own family, the Kogiidae, leaving the Physeteridae as a monotypic family, although additional fossil representatives of both families are known.

<span class="mw-page-title-main">Kogiidae</span> Family of mammals

Kogiidae is a family comprising at least two extant species of Cetacea, the pygmy and dwarf sperm whales. As their common names suggest, they somewhat resemble sperm whales, with squared heads and small lower jaws, but are much smaller in size, with much shorter skulls and more notable dorsal fins than sperm whales. Kogiids are also characterized by a "false gill slit" behind their eyes.

<span class="mw-page-title-main">Toothed whale</span> Parvorder of cetaceans

The toothed whales are a parvorder of cetaceans that includes dolphins, porpoises, and all other whales possessing teeth, such as the beaked whales and sperm whales. 73 species of toothed whales are described. They are one of two living groups of cetaceans, the other being the baleen whales (Mysticeti), which have baleen instead of teeth. The two groups are thought to have diverged around 34 million years ago (mya).

<span class="mw-page-title-main">Northern bottlenose whale</span> Species of mammal

The northern bottlenose whale is a species of beaked whale in the ziphiid family, being one of two members of the genus Hyperoodon. The northern bottlenose whale was hunted heavily by Norway and Britain in the 19th and early 20th centuries. It is one of the deepest-diving mammals known, reaching depths of 2,339 m (7,674 ft) and capable of diving for up to 130 minutes.

<span class="mw-page-title-main">Pygmy sperm whale</span> Species of mammal

The pygmy sperm whale is one of two extant species in the family Kogiidae in the sperm whale superfamily. They are not often sighted at sea, and most of what is known about them comes from the examination of stranded specimens.

<span class="mw-page-title-main">Dwarf sperm whale</span> Species of whale

The dwarf sperm whale is a sperm whale that inhabits temperate and tropical oceans worldwide, in particular continental shelves and slopes. It was first described by biologist Richard Owen in 1866, based on illustrations by naturalist Sir Walter Elliot. The species was considered to be synonymous with the pygmy sperm whale from 1878 until 1998. The dwarf sperm whale is a small whale, 2 to 2.7 m and 136 to 272 kg, that has a grey coloration, square head, small jaw, and robust body. Its appearance is very similar to the pygmy sperm whale, distinguished mainly by the position of the dorsal fin on the body–nearer the middle in the dwarf sperm whale and nearer the tail in the other.

<i>Ancistrocheirus</i> Genus of squids

Ancistrocheirus lesueurii, the sharpear enope squid, is the only species in the genus Ancistrocheirus and family Ancistrocheiridae. With a mantle length of 25 cm (9.8 in), this moderately sized squid may be found throughout the tropical and subtropical oceans. They tend to be found at mesopelagic depths.

<span class="mw-page-title-main">Spermaceti organ</span> Part of a sperm whale

The spermaceti organ is an organ present in the heads of toothed whales of the family Physeteroidea, in particular the sperm whale. This organ contains a waxy liquid called spermaceti and is involved in the generation of sound.

<i>Zygophyseter</i> Extinct genus of sperm whales

Zygophyseter varolai is an extinct sperm whale that lived during the Tortonian age of the Late Miocene 11.2 to 7.6 million years ago. It is known from a single specimen from the Pietra Leccese Formation in Italy. It was a member of a stem group of fossil macroraptorial sperm whales also including Brygmophyseter, Acrophyseter, and Livyatan. It probably grew to be around 6.5 to 7 meters in length and shared some characteristics with other raptorials, such as large teeth with tooth enamel that were functional in both the upper and lower jaws which the modern sperm whale lacks. It also had a beak, the ability to echolocate prey, and could have probably swum faster than the modern-day sperm whale which can reach 4 kilometers per hour (2.5 mph). These were probably used in the capture of large prey, such as large fish, seals, and whales. In fact, its common name, the killer sperm whale, refers to its feeding habits that would have had a resemblance to the modern-day killer whale.

<i>Brygmophyseter</i> Extinct genus of toothed whale (fossil)

Brygmophyseter, known as the biting sperm whale, is an extinct genus of toothed whale in the sperm whale family with one species, B. shigensis. When it was first described in 1994, the species was placed in the genus Scaldicetus based on tooth morphology, but this was later revised in 1995. In 2006, it was classified into the genus Naganocetus, which is considered to be a junior synonym. The only known specimen, a nearly complete skeleton, was dated to be around 16–15 million years old. Brygmophyseter is thought to have been 6.5–7 meters (21–23 ft) long, and it probably had 11 or 12 teeth in the upper and lower jaws. Brygmophyseter is part of a group of macroraptorial sperm whales which tended to be apex predators using their large teeth to catch struggling prey such as whales. It had a spermaceti organ which was probably used for biosonar like in the modern sperm whale. The whale has made an appearance on The History Channel's TV series Jurassic Fight Club.

<span class="mw-page-title-main">Sperm whaling</span> Human hunting of sperm whales

Sperm whaling is the human practice of hunting sperm whales, the largest toothed whale and the deepest-diving marine mammal species, for the oil, meat and bone that can be extracted from the cetaceans' bodies.

<i>Livyatan</i> Extinct genus of sperm whale from the Miocene epoch

Livyatan is an extinct genus of macroraptorial sperm whale containing one known species: L. melvillei. The genus name was inspired by the biblical sea monster Leviathan, and the species name by Herman Melville, the author of the famous novel Moby-Dick about a white bull sperm whale. It is mainly known from the Pisco Formation of Peru during the Tortonian stage of the Miocene epoch, about 9.9–8.9 million years ago (mya); however, finds of isolated teeth from other locations such as Chile, Argentina, United States (California), South Africa and Australia imply that either it or a close relative survived into the Pliocene, around 5 mya, and may have had a global presence. It was a member of a group of macroraptorial sperm whales and was probably an apex predator, preying on whales, seals and so forth. Characteristically of raptorial sperm whales, Livyatan had functional, enamel-coated teeth on the upper and lower jaws, as well as several features suitable for hunting large prey.

<i>Acrophyseter</i> Extinct genus of sperm whales

Acrophyseter is a genus of extinct sperm whales that lived in the Late Miocene off the coast of Peru comprising two species: A. deinodon and A. robustus. It is part of a group of macroraptorial sperm whales which all shared several features for the purpose of hunting large prey, such as deeply rooted and thick teeth. Acrophyseter measured 4–4.5 metres (13–15 ft), making it the smallest raptorial sperm whale. Because of its short pointed snout, and its strong curved front teeth, it probably fed on the large marine vertebrates of its time, such as seals and other whales.

<i>Taonius pavo</i> Species of squid

Taonius pavo is a species of glass squid found in the Atlantic Ocean. Its exact geographic distribution is uncertain, but it may extend to the southwestern Indian Ocean through the Agulhas Current.

<i>Albicetus</i> Extinct genus of mammals

Albicetus is a genus of stem-sperm whales that lived during the Miocene Epoch, around 15 million years ago, and was discovered in Santa Barbara, California in 1909. It was categorized for decades as belonging to a group of extinct walruses erroneously thought to be sperm whales. It was named Albicetus, meaning "white whale", is a reference to the leviathan in Herman Melville's classic 1851 novel Moby-Dick.

<span class="mw-page-title-main">Macroraptorial sperm whale</span> Predatory family of extinct whales

Macroraptorial sperm whales were highly predatory whales of the sperm whale superfamily (Physeteroidea) of the Miocene epoch that hunted large marine mammals, including other whales, using their large teeth. They consist of five genera: Acrophyseter, Albicetus, Brygmophyseter, Livyatan, and Zygophyseter. All species are known by at least a skull, and are informally grouped without a family designation. They were all likely the apex predator of their habitats, comparable to the modern day killer whale, and achieved great lengths, with one species–Livyatan–measuring about 13.5–17.5 m (44–57 ft).

References

  1. Mead, J. G.; Brownell, R. L. Jr. (2005). "Order Cetacea". In Wilson, D. E.; Reeder, D. M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 737. ISBN   978-0-8018-8221-0. OCLC   62265494.
  2. "Physeter macrocephalus Linnaeus 1758 (sperm whale)". Fossilworks: Gateway to the Paleobiology Database. Retrieved 17 December 2021.
  3. 1 2 3 4 5 6 7 8 9 10 Taylor, B.L.; Baird, R.; Barlow, J.; Dawson, S.M.; Ford, J.; Mead, J.G.; Notarbartolo di Sciara, G.; Wade, P.; Pitman, R.L. (2019). "Physeter macrocephalus". IUCN Red List of Threatened Species . 2019: e.T41755A160983555. doi: 10.2305/IUCN.UK.2008.RLTS.T41755A160983555.en . Retrieved 19 November 2021.
  4. 1 2 "Appendices | CITES". cites.org. Retrieved 14 January 2022.
  5. "Sperm Whale". acsonline.org. Archived from the original on 22 April 2017. Retrieved 13 May 2017.
  6. 1 2 Gregory S. Schorr; Erin A. Falcone; David J. Moretti; Russel D. Andrews (2014). "First long-term behavioral records from Cuvier's beaked whales (Ziphius cavirostris) reveal record-breaking dives". PLOS One . 9 (3): e92633. Bibcode:2014PLoSO...992633S. doi: 10.1371/journal.pone.0092633 . PMC   3966784 . PMID   24670984.
  7. 1 2 "Census of Marine Life – From the Edge of Darkness to the Black Abyss" (PDF). Coml.org. Retrieved 15 December 2009.
  8. Møhl, Bertel; Wahlberg, Magnus; Peter T. Madsen (2003). "The monopulsed nature of sperm whale clicks". The Journal of the Acoustical Society of America. 114 (2): 1143–1154. Bibcode:2003ASAJ..114.1143M. doi:10.1121/1.1586258. PMID   12942991.
  9. Trivedi, Bijal P. (3 November 2003). "Sperm Whale "Voices" Used to Gauge Whales' Sizes". National Geographic. Archived from the original on 6 November 2003.
  10. 1 2 3 4 5 6 7 8 9 10 11 Shirihai, H. & Jarrett, B. (2006). Whales, Dolphins, and Other Marine Mammals of the World. Princeton: Princeton Univ. Press. pp. 21–24. ISBN   978-0-691-12757-6.
  11. 1 2 3 4 5 6 Reeves, R.; Stewart, B.; Clapham, P. & Powell, J. (2003). Guide to Marine Mammals of the World. New York: A.A. Knopf. pp.  240–243. ISBN   978-0-375-41141-0.
  12. 1 2 Whitehead, H. & Weilgart, L. (2000). "The Sperm Whale". In Mann, J.; Connor, R.; Tyack, P. & Whitehead, H. (eds.). Cetacean Societies. The University of Chicago Press. p.  169. ISBN   978-0-226-50341-7.
  13. Spitznagel, Eric (12 January 2012). "Ambergris, Treasure of the Deep". Bloomberg L.P. Retrieved 25 May 2017.
  14. Wahlberg, Magnus; Frantzis, Alexandros; Alexiadou, Paraskevi; Madsen, Peter T.; Møhl, Bertel (2005). "Click production during breathing in a sperm whale (Physeter macrocephalus)". The Journal of the Acoustical Society of America. 118 (6): 3404–7. Bibcode:2005ASAJ..118.3404W. doi:10.1121/1.2126930. PMID   16419786.
  15. Haupt, Paul (1907). "Jonah's Whale". Proceedings of the American Philosophical Society. 46 (185): 151–164. JSTOR   983449.
  16. Fеrnandez-Casado, M. (2000). "El Cachalote (Physeter macrocephalus)" (PDF). Galemys. 12 (2): 3. Archived from the original (PDF) on 7 August 2020. Retrieved 27 September 2013.
  17. Corominas, Joan (1987). Breve diccionario etimológico de la lengua castellana. Madrid: Gredos. ISBN   978-84-249-1332-8.
  18. Encarta Dictionary
  19. Crabb, George (1823). Universal Technological Dictionary Or Familiar Explanation of the Terms Used in All Arts and Sciences: Containing Definitions Drawn from the Original Writers : in Two Volumes. Baldwin, Cradock & Joy. p. 333.
  20. Ridgway, Sam H. (1989). Handbook of Marine Mammals. Academic Press. p. 179. ISBN   978-0-12-588504-1. The earliest available species-group name for a Southern Hemisphere sperm whale is Physeter australasianus Desmoulins, 1822.
  21. Agnarsson, I.; May-Collado, LJ. (2008). "The phylogeny of Cetartiodactyla: the importance of dense taxon sampling, missing data, and the remarkable promise of cytochrome b to provide reliable species-level phylogenies". Mol Phylogenet Evol. 48 (3): 964–985. doi:10.1016/j.ympev.2008.05.046. PMID   18590827.
  22. Price, SA.; Bininda-Emonds, OR.; Gittleman, JL. (2005). "A complete phylogeny of the whales, dolphins and even-toed hoofed mammals (Cetartiodactyla)". Biol Rev Camb Philos Soc. 80 (3): 445–473. doi:10.1017/s1464793105006743. PMID   16094808. S2CID   45056197.
  23. Montgelard, C.; Catzeflis, FM.; Douzery, E. (1997). "Phylogenetic relationships of artiodactyls and cetaceans as deduced from the comparison of cytochrome b and 12S RNA mitochondrial sequences". Molecular Biology and Evolution. 14 (5): 550–559. doi: 10.1093/oxfordjournals.molbev.a025792 . PMID   9159933.
  24. Spaulding, M.; O'Leary, MA.; Gatesy, J. (2009). "Relationships of Cetacea (Artiodactyla) Among Mammals: Increased Taxon Sampling Alters Interpretations of Key Fossils and Character Evolution". PLOS ONE. 4 (9): e7062. Bibcode:2009PLoSO...4.7062S. doi: 10.1371/journal.pone.0007062 . PMC   2740860 . PMID   19774069.
  25. "Society for Marine Mammalogy". The Insomniac Society.
  26. Mead, J. G.; Brownell, R. L. Jr. (2005). "Order Cetacea". In Wilson, D. E.; Reeder, D. M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. pp. 723–743. ISBN   978-0-8018-8221-0. OCLC   62265494.
  27. 1 2 3 4 Lambert, O.; Bianucci, G. & de Muizon, C. (August 2008). "A new stem-sperm whale (Cetacea, Odontoceti, Physeteroidea) from the Latest Miocene of Peru". Comptes Rendus Palevol. 7 (6): 361–369. Bibcode:2008CRPal...7..361L. doi:10.1016/j.crpv.2008.06.002. S2CID   85723286.
  28. Artedi, Peter (1730). Genera piscium : in quibus systema totum ichthyologiae proponitur cum classibus, ordinibus, generum characteribus, specierum differentiis, observationibus plurimis : redactis speciebus 242 ad genera 52 : Ichthyologiae pars III (in Latin). Grypeswaldiae : Impensis Ant. Ferdin. Röse. pp.  553–555.
  29. Linnaeus, Carolus (1758). Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata (in Latin). Holmiae. (Laurentii Salvii). p. 824.
  30. Holthuis L. B. (1987). "The scientific name of the sperm whale". Marine Mammal Science. 3 (1): 87–89. Bibcode:1987MMamS...3...87H. doi:10.1111/j.1748-7692.1987.tb00154.x.
  31. Schevill W.E. (1986). "The International Code of Zoological Nomenclature and a paradigm – the name Physeter catodon Linnaeus 1758". Marine Mammal Science. 2 (2): 153–157. Bibcode:1986MMamS...2..153S. doi:10.1111/j.1748-7692.1986.tb00036.x.
  32. Schevill W.E. (1987). "Reply to L. B. Holthuis "The scientific name of the sperm whale". Marine Mammal Science. 3 (1): 89–90. doi:10.1111/j.1748-7692.1987.tb00155.x.
  33. "ITIS Standard Report Page: Physeter catodon" . Retrieved 19 January 2015.
  34. Husson A.M.; Holthuis L.B. (1974). "Physeter macrocephalus Linnaeus, 1758, the valid name for the sperm whale". Zoologische Mededelingen. 48: 205–217.
  35. Whitehead, p. 3
  36. "List of Marine Mammal Species and Subspecies". marinemammalscience.org. 13 November 2016. Retrieved 25 May 2017.
  37. 1 2 Hal Whitehead (2003). "17 – Society and Culture in the Deep and Open Ocean: The Sperm Whale and Other Cetaceans". In Frans B. M. de Waal; Peter L. Tyack (eds.). Animal Society Complex: Intelligence, Culture, and Individualized Societies. Harvard University Press. p. 448. doi:10.4159/harvard.9780674419131.c34. ISBN   9780674419131.
  38. 1 2 3 4 5 6 7 McClain, Craig R.; Balk, Meghan A.; Benfield, Mark C.; Branch, Trevor A.; Chen, Catherine; Cosgrove, James; Dove, Alistair D.M.; Gaskins, Leo; Helm, Rebecca R.; Hochberg, Frederick G.; Lee, Frank B.; Marshall, Andrea; McMurray, Steven E.; Schanche, Caroline; Stone, Shane N.; Thaler, Andrew D. (13 January 2015). "Sizing ocean giants: patterns of intraspecific size variation in marine megafauna". PeerJ. 3: e715. doi: 10.7717/peerj.715 . PMC   4304853 . PMID   25649000.
  39. 1 2 3 4 5 6 7 8 9 Whitehead, H. (2002). "Sperm whale Physeter macrocephalus". In Perrin, W.; Würsig B.; Thewissen, J. (eds.). Encyclopedia of Marine Mammals. Academic Press. pp.  1165–1172. ISBN   978-0-12-551340-1.
  40. 1 2 Nowak, R.M.; Walker, E.P. (2003). Walker's marine mammals of the world. JHU Press. ISBN   9780801873430.
  41. Ruelas-Inzunza, J; Páez-Osuna, F (September 2002). "Distribution of Cd, Cu, Fe, Mn, Pb and Zn in selected tissues of juvenile whales stranded in the SE Gulf of California (Mexico)". Environment International. 28 (4): 325–329. doi:10.1016/s0160-4120(02)00041-7. PMID   12220119.
  42. 1 2 3 Dufault, S.; Whitehead, H.; Dillon, D. (1999). "An examination of the current knowledge on the stock structure of sperm whales (Physeter macrocephalus) worldwide". Journal of Cetacean Research and Management. 1 (1): 1–10. doi: 10.47536/jcrm.v1i1.447 . S2CID   256290992.
  43. Clarke, R.; Paliza, O.; Van Waerebeek, K. (2011). "Sperm whales of the Southeast Pacific. Part VII. Reproduction and growth in the female". Latin American Journal of Aquatic Mammals. 10 (1): 8–39. doi: 10.5597/lajam00172 .
  44. Omura, H. (1950). "On the Body Weight of Sperm and Sei Whales located in the Adjacent Waters of Japan". Scientific Reports of the Whales Research Institute, Tokyo. 4: 27–113.
  45. 1 2 Ellis, Richard (2011). The Great Sperm Whale: A Natural History of the Ocean's Most Magnificent and Mysterious Creature. Zoology. Vol. 179. USA: University Press of Kansas. p.  432. ISBN   978-0-7006-1772-2. Zbl   0945.14001.
  46. Shirihai, H. & Jarrett, B. (2006). Whales, Dolphins, and Other Marine Mammals of the World. Princeton: Princeton Univ. Press. pp. 112–115. ISBN   978-0-691-12757-6.
  47. 1 2 3 4 Wood, Gerald (1983). The Guinness Book of Animal Facts and Feats . Guinness Superlatives. p.  256. ISBN   978-0-85112-235-9.
  48. 1 2 Carwardine, Mark. (1995). The Guinness book of Animal records. Enfield: Guinness Publishing. ISBN   978-0851126586. OCLC   60244977.
  49. Maury, M. (1853). Explanations and Sailing Directions to Accompany the Wind and Current Charts. C. Alexander. p. 297.
  50. Kasuya, Toshio (July 1991). "Density dependent growth in North Pacific sperm whales". Marine Mammal Science. USA: Wiley. 7 (3): 230–257. Bibcode:1991MMamS...7..230K. doi:10.1111/j.1748-7692.1991.tb00100.x.
  51. Richards, Rhys, "Sperm whaling on the Solanders Grounds and in Fiordland – A maritime historian's perspective" (PDF), NIWA, NIWA Information Series No. 76
  52. Gordon, Jonathan (1998). Sperm Whales, Voyageur Press, p. 14, ISBN   0-89658-398-8
  53. Carwardine, Mark (1994). On the Trail of the Whale . Chapter 1. Thunder Bay Publishing Co. ISBN   978-1-899074-00-6.
  54. "Offshore Cetacean Species". CORE. Archived from the original on 16 May 2008. Retrieved 12 October 2008.
  55. How does pressure change with ocean depth?. Oceanservice.noaa.gov (11 January 2013). Retrieved 2013-03-19.
  56. Moore MJ, Early GA (2004). "Cumulative sperm whale bone damage and the bends". Science . 306 (5705): 2215. doi:10.1126/science.1105452. PMID   15618509. S2CID   39673774.
  57. Parsons, Edward C. M.; Parsons, ECM; Bauer, A.; Simmonds, M. P.; Wright, A. J.; McCafferty, D. (2013). An Introduction to Marine Mammal Biology and Conservation. Jones & Bartlett Publishers. ISBN   9780763783440.
  58. The science behind whales' asymmetrical skulls. Io9.com. Retrieved 2013-03-19.
  59. 1 2 Jefferson, T.A.; Webber, M.A. & Pitman, R.L. (2008). Marine Mammals of the World: a comprehensive guide to their identification. London: Elsevier. pp. 74–78. ISBN   978-0-12-383853-7.
  60. "Sperm Wale Physeter macrocephalus". American Cetacean Society Fact Sheet. Archived from the original on 13 June 2010.
  61. "Sperm Whale Facts". whale-images.com. Archived from the original on 15 January 2010. Retrieved 27 December 2007.
  62. Whitehead, p. 4
  63. Perrin, p. 8
  64. "Sperm Whales (Physeter macrocephalus)". U.S. Department of Commerce NOAA Office of Protected Resources. Retrieved 7 November 2008.
  65. 1 2 Marino, L. (2004). "Cetacean Brain Evolution Multiplication Generates Complexity" (PDF). International Journal of Comparative Psychology. 17: 3–4. doi:10.46867/IJCP.2004.17.01.06. Archived from the original (PDF) on 20 November 2012. Retrieved 10 August 2013.
  66. Fields, R. Douglas (15 January 2008). Are Whales Smarter Than We Are? Scientific American.
  67. Whitehead, p. 323
  68. Dicke, U.; Roth, G. (August–September 2008). "Intelligence Evolved". Scientific American Mind. Vol. 19, no. 4. pp. 71–77. doi:10.1038/scientificamericanmind0808-70.
  69. Oelschläger, Helmut H.A.; Kemp, Birgit (1998). "Ontogenesis of the sperm whale brain". The Journal of Comparative Neurology. 399 (2): 210–28. doi:10.1002/(SICI)1096-9861(19980921)399:2<210::AID-CNE5>3.0.CO;2-3. PMID   9721904. S2CID   23821591.
  70. Kooyman, G. L. & Ponganis, P. J. (October 1998). "The Physiological Basis of Diving to Depth: Birds and Mammals". Annual Review of Physiology. 60 (1): 19–32. doi:10.1146/annurev.physiol.60.1.19. PMID   9558452.
  71. Tyack, P.; Johnson, M.; Aguilar Soto, N.; Sturlese, A. & Madsen, P. (18 October 2006). "Extreme diving of beaked whales". Journal of Experimental Biology. 209 (Pt 21): 4238–4253. doi: 10.1242/jeb.02505 . PMID   17050839.
  72. Cawardine, Mark (2002) Sharks and Whales, Five Mile Press, p. 333, ISBN   1-86503-885-7
  73. Whitehead, pp. 156–161
  74. Ommanney, F. 1971. Lost Leviathan. London.
  75. Inside Natures Giants: The Sperm Whale. Channel 4
  76. 1 2 "Whale Digestion". Chip.choate.edu. Archived from the original on 23 October 2013. Retrieved 23 July 2013.
  77. Tinker, Spencer Wilkie (1988). Whales of the World. Brill Archive, p. 62, ISBN   0-935848-47-9
  78. "20000 Leagues Under the Sea Part2 Ch12 | Nikolaus6's Weblog". Nikolaus6.wordpress.com. 18 July 2008. Retrieved 23 July 2013.
  79. 1 2 Archived at Ghostarchive and the Wayback Machine : Professor Malcolm Clarke – discusses the anatomy of sperm whales. 25 April 2011 via YouTube.
  80. Race, George J.; Edwards, W. L. Jack; Halden, E. R.; Wilson, Hugh E.; Luibel, Francis J. (1959). "A Large Whale Heart". Circulation. 19 (6): 928–932. doi: 10.1161/01.cir.19.6.928 . PMID   13663185.
  81. Shadwick RE, Gosline JM (1995). "Arterial Windkessels in marine mammals". Symposia of the Society for Experimental Biology. 49: 243–52. PMID   8571227.
  82. 1 2 Melnikov VV (October 1997). "The arterial system of the sperm whale (Physeter macrocephalus)". Journal of Morphology. 234 (1): 37–50. doi:10.1002/(SICI)1097-4687(199710)234:1<37::AID-JMOR4>3.0.CO;2-K. PMID   9329202. S2CID   35438320.
  83. Lee, Jane J. (26 March 2014). "Elusive Whales Set New Record for Depth and Length of Dives Among Mammals". National Geographic. Archived from the original on 29 March 2014.
  84. Dunham, Will (26 March 2014). "How low can you go? This whale is the champion of deep diving". Reuters via www.reuters.com.
  85. "The Globe and Mail". The Globe and Mail . Archived from the original on 25 June 2014. Retrieved 18 February 2020.
  86. Harrison, R. J. (10 May 1962). "Seals as divers". New Scientist. Reed Business Information. 14 (286).
  87. Noren, S. R. & Williams, T. M. (June 2000). "Body size and skeletal muscle myoglobin of cetaceans: adaptations for maximizing dive duration". Comparative Biochemistry and Physiology – Part A: Molecular & Integrative Physiology. 126 (2): 181–191. doi:10.1016/S1095-6433(00)00182-3. PMID   10936758.
  88. Marshall, C. "Morphology, Functional; Diving Adaptations of the Cardiovascular System", p. 770 in Perrin
  89. "Aquarium of the Pacific – Sperm Whale". Aquarium of the Pacific. Archived from the original on 14 March 2019. Retrieved 6 November 2008.
  90. Shwartz, Mark (8 March 2007). "Scientists conduct first simultaneous tagging study of deep-diving predator, prey". Stanford Report. Retrieved 6 November 2008.
  91. 1 2 Clarke, M. (1978). "Structure and Proportions of the Spermaceti Organ in the Sperm Whale" (PDF). Journal of the Marine Biological Association of the United Kingdom. 58 (1): 1–17. Bibcode:1978JMBUK..58....1C. doi:10.1017/S0025315400024371. S2CID   17892285. Archived from the original (PDF) on 17 December 2008. Retrieved 5 November 2008.
  92. 1 2 Worthington, L. V.; Schevill, William E. (August 1957). "Underwater Sounds heard from Sperm Whales". Nature. 180 (4580): 291. Bibcode:1957Natur.180..291W. doi: 10.1038/180291a0 . S2CID   4173897.
  93. 1 2 Cranford, T.W. (2000). "In Search of Impulse Sound Sources in Odontocetes". In Au, W.W.L; Popper, A.N.; Fay, R.R. (eds.). Hearing by Whales and Dolphins (Springer Handbook of Auditory Research series). Springer-Verlag, New York. ISBN   978-0-387-94906-2.
  94. Norris, K.S. & Harvey, G.W. (1972). "A theory for the function of the spermaceti organ of the sperm whale". In Galler, S.R; Schmidt-Koenig, K; Jacobs, G.J. & Belleville, R.E. (eds.). Animal orientation and navigation. NASA, Washington, D.C. pp. 397–417.
  95. 1 2 Cranford, T.W. (1999). "The Sperm Whale's Nose: Sexual Selection on a Grand Scale?". Marine Mammal Science. 15 (4): 1133–1157. Bibcode:1999MMamS..15.1133C. doi:10.1111/j.1748-7692.1999.tb00882.x.
  96. Madsen, P.T.; Payne, R.; Kristiansen, N.U.; Wahlberg, M.; Kerr, I. & Møhl, B. (2002). "Sperm whale sound production studied with ultrasound time/depth-recording tags". Journal of Experimental Biology. 205 (Pt 13): 1899–1906. doi:10.1242/jeb.205.13.1899. PMID   12077166.
  97. Møhl, B.; Wahlberg, M.; Madsen, P.T.; Miller, L.A. & Surlykke, A. (2000). "Sperm whale clicks: directionality and sound levels revisited". Journal of the Acoustical Society of America. 107 (1): 638–648. Bibcode:2000ASAJ..107..638M. doi:10.1121/1.428329. PMID   10641672. S2CID   9610645.
  98. Møhl, B.; Wahlberg, M.; Madsen, P.T.; Heerfordt, A. & Lund, A. (2003). "The monopulsed nature of sperm whale clicks". Journal of the Acoustical Society of America. 114 (2): 1143–1154. Bibcode:2003ASAJ..114.1143M. doi:10.1121/1.1586258. PMID   12942991.
  99. Whitehead, pp. 277–279
  100. Stefan Huggenberger; Michel Andre & Helmut H. A. Oelschlager (2014). "The nose of the sperm whale – overviews of functional design, structural homologies and evolution". Journal of the Marine Biological Association of the United Kingdom. 96 (4): 1–24. doi:10.1017/S0025315414001118. hdl: 2117/97052 . S2CID   27312770.
  101. Taxonomy | Natural History Museum. . Retrieved 2013-03-19.
  102. Whitehead, p. 321
  103. Perrin, p. 1164
  104. Morris, Robert J. (1975). "Further studies into the lipid structure of the spermaceti organ of the sperm whale (Physeter catodon)". Deep-Sea Research. 22 (7): 483–489. Bibcode:1975DSRA...22..483M. doi: 10.1016/0011-7471(75)90021-2 .
  105. 1 2 3 Norris, Kenneth S. & Harvey, George W. (1972). "A Theory for the Function of the Spermaceti Organ of the Sperm Whale". Animal orientation and navigation. NASA.
  106. 1 2 3 4 Carrier, David R.; Deban, Stephen M.; Otterstrom, Jason (15 June 2002). "The face that sank the Essex : potential function of the spermaceti organ in aggression". Journal of Experimental Biology. 205 (12): 1755–1763. doi:10.1242/jeb.205.12.1755. PMID   12042334.
  107. "Science Says Sperm Whales Could Really Wreck Ships". Popular Science. 8 April 2016. Retrieved 13 April 2016.
  108. Panagiotopoulou, Olga; Spyridis, Panagiotis; Abraha, Hyab Mehari; Carrier, David R.; Pataky, Todd C. (2016). "Architecture of the sperm whale forehead facilitates ramming combat". PeerJ. 4: e1895. doi: 10.7717/peerj.1895 . PMC   4824896 . PMID   27069822.
  109. Cranford, T. W.; Amundin, M.; Norris, K. S. (1996). "Functional morphology and homology in the odontocete nasal complex: Implications for sound generation". Journal of Morphology. 228 (3): 223–285. doi:10.1002/(SICI)1097-4687(199606)228:3<223::AID-JMOR1>3.0.CO;2-3. PMID   8622183. S2CID   35653583.
  110. Clarke, M. (1978). "Physical Properties of Spermaceti Oil in the Sperm Whale" (PDF). Journal of the Marine Biological Association of the United Kingdom. 58 (1): 19–26. Bibcode:1978JMBUK..58...19C. doi:10.1017/S0025315400024383. S2CID   3563596. Archived from the original (PDF) on 17 December 2008. Retrieved 5 November 2008.
  111. Clarke, M.R. (November 1970). "Function of the Spermaceti Organ of the Sperm Whale". Nature. 228 (5274): 873–874. Bibcode:1970Natur.228..873C. doi:10.1038/228873a0. PMID   16058732. S2CID   4197332.
  112. Whitehead, pp. 317–321
  113. "Spermaceti as battering ram?" (PDF). Archived from the original (PDF) on 2 October 2006. Retrieved 19 March 2007.
  114. Bjerager, P.; Heegaard, S. & Tougaar, J. (2003). "Anatomy of the eye of the sperm whale (Physeter macrocephalus L.)". Aquatic Mammals. 29 (1): 31–36. doi:10.1578/016754203101024059.
  115. Bjerager, Poul; Heegaard, Steffen; Tougaard, Jakob (2003). "Anatomy of the eye of the sperm whale (Physeter macrocephalus L.)". Aquatic Mammals. 29 (1): 31–36. doi:10.1578/016754203101024059.
  116. Fristrup, K. M.; Harbison, G. R. (2002). "How do sperm whales catch squids?". Marine Mammal Science. 18 (1): 42–54. Bibcode:2002MMamS..18...42F. doi: 10.1111/j.1748-7692.2002.tb01017.x .
  117. Gibbens, Sarah (5 August 2017). "Photo Shows How Sperm Whales Sleep". National Geographic . Archived from the original on 1 March 2021. Retrieved 25 June 2021.
  118. Howard, Jacqueline (8 September 2012). "Sperm Whales Sleep While 'Drifting' Vertically, Scientists Say (VIDEO)". HuffPost . Retrieved 8 February 2013.
  119. Árnason, U. (2009). "Banding studies on the gray and sperm whale karyotypes". Hereditas. 95 (2): 277–281. doi: 10.1111/j.1601-5223.1981.tb01418.x . PMID   7309542.
  120. "SEASWAP: Genetic Sampling". Seaswap.info. Archived from the original on 5 January 2009. Retrieved 23 July 2013.
  121. Davies, Ella. "The world's loudest animal might surprise you". BBC. Retrieved 13 January 2020.
  122. Backus, R.H.; Schevill, W.E. (1966). "Physeter clicks". In Norris, K.S. (ed.). Whales, dolphins and porpoises. University of California Press, Berkeley, California. pp. 510–527.
  123. Goold, J.C. (1996). "Signal processing techniques for acoustic measurement of sperm whale body lengths". Journal of the Acoustical Society of America. 100 (5): 3431–3441. Bibcode:1996ASAJ..100.3431G. doi:10.1121/1.416984. PMID   8914321.
  124. 1 2 Gordon, J.C.D. (1991). "Evaluating a method for determining the length of sperm whales (Physeter catodon) from their vocalizations". Journal of Zoology, London. 224 (2): 301–314. doi:10.1111/j.1469-7998.1991.tb04807.x.
  125. Whitlow, W. "Echolocation", pp. 359–367 in Perrin
  126. "Whale Sounds". Museum of New Zealand Te Papa Tongarewa. 19 January 2018.
  127. Fais, A.; Aguilar Soto, N.; Johnson, M.; Pérez-González, C.; Miller, P. J. O.; Madsen, P. T. (April 2015). "Sperm whale echolocation behaviour reveals a directed, prior-based search strategy informed by prey distribution". Behavioral Ecology and Sociobiology. 69 (4): 663–674. doi:10.1007/s00265-015-1877-1. hdl: 10023/8168 . PMID   12077166. S2CID   13711121.
  128. 1 2 3 4 Whitehead, p. 135
  129. Whitehead, p. 144
  130. 1 2 3 4 5 Hal Whitehead (2024). "Sperm whale clans and human societies". Royal Society Open Science . doi:10.1098/rsos.231353. PMC   10776220 .
  131. 1 2 3 4 Taylor A. Hersh; et al. (2022). "Evidence from sperm whale clans of symbolic marking in non-human cultures". PNAS . National Academy of Sciences. 119 (37): e2201692119. doi:10.1073/pnas.2201692119. hdl: 10023/27122 .
  132. 1 2 Gero, Shane; Whitehead, Hal; Rendell, Luke (2016). "Individual, unit and vocal clan level identity cues in sperm whale codas". Royal Society Open Science . doi:10.1098/rsos.150372. hdl: 10023/8071 .
  133. 1 2 Safina, Carl (2020). Becoming Wild: How Animal Cultures Raise Families, Create Beauty, and Achieve Peace. Henry Holt and Company. pp. 16–19. ISBN   9781250173331.
  134. 1 2 "Cultural identity in sperm whales". PNAS. National Academy of Sciences. 5 December 2022. Retrieved 7 February 2024.
  135. Cantor, Maurício; Whitehead, Hal (October 2015). "How does social behavior differ among sperm whale clans?". Marine Mammal Science. 31 (4): 1275–1290. Bibcode:2015MMamS..31.1275C. doi:10.1111/mms.12218.
  136. Obaldía, Carlos De; Simkus, Gediminas; Zölzer, Udo (March 2015). Estimating the number of sperm whale (Physeter macrocephalus) individuals based on grouping of corresponding clicks. 41. Deutsche Jahrestagung für Akustik, (DAGA 2015). ResearchGate GmbH. Nuremberg. doi:10.13140/RG.2.1.3764.9765.
  137. Bester L., ed. (2015). "Mornington Peninsula Biodiversity: Survey and Research Highlights". Caulton S. Et Al. The Shire of Mornington Peninsula . Retrieved 16 August 2016.
  138. Whitehead, p. 33
  139. Murray, J. W.; Jannasch, H. W.; Honjo, S.; Anderson, R. F.; Reeburgh, W. S.; Top, Z.; Friederich, G. E.; Codispoti, L. A. & Izdar E. (30 March 1989). "Unexpected changes in the oxic/anoxic interface in the Black Sea". Nature. 338 (6214): 411–413. Bibcode:1989Natur.338..411M. doi:10.1038/338411a0. S2CID   4306135.
  140. Irfan M. 2017. First live sperm whales sighted in Pakistani waters: WWF (VIDEO). Daily Pakistan. Retrieved 21 September 2017
  141. Minton G.. 2017. Sperm whales and blue whales sighted by fishermen off the coast of Pakistan. Arabian Sea Whale Network. Retrieved 21 September 2017
  142. 엄기영. 김주하. 2005. 전남 신안군 우의도, 길이 16m 무게 40톤 초대형 고래 죽은채 발견[김양훈. MBC뉴스. Retrieved 7 October 2017
  143. 1 2 우연과 인연. 2005. 윗 글 향고래 Archived 6 October 2017 at the Wayback Machine . Daum. Retrieved 7 October 2017
  144. 2015. [단독] 강화 해변서 최후 맞은 향고래…6년만에 '부활'. No Cut News. Retrieved 7 October 2017
  145. 1 2 Whitehead, pp. 23–24
  146. "陸からクジラの潮吹きがわかる!「クジラの見える丘」". 世界遺産知床情報局. ニッポン旅マガジン. 16 August 2015. Archived from the original on 17 August 2017. Retrieved 16 August 2016.
  147. Archived at Ghostarchive and the Wayback Machine : "相模湾にマッコウクジラとみられる群れ/神奈川新聞(カナロコ)" via YouTube.
  148. vegan1110. "エコツアー風景 -イルカ・クジラ・ネイチャー ウォッチングセンター:静岡県伊東市城ヶ崎 富戸港 – 光海丸で行く、本当の大自然との、"ふれあい"。- ドルフィンウォッチング、エコツーリスト、エコツーリズム KOHKAIMARU 石井泉 光海丸". Archived from the original on 3 March 2016.{{cite web}}: CS1 maint: numeric names: authors list (link)
  149. Archived at Ghostarchive and the Wayback Machine : "相模湾でマッコウクジラに遭遇 Sperm Whale Encounter in Japan" via YouTube.
  150. "琉球諸島". くじらガイドがお届けするクジラ・シャチ・イルカ・自然・エコツアー情報.
  151. "ޥåη졪". '̣ ϡȥɤΥۥ.
  152. Archived at Ghostarchive and the Wayback Machine : "Guam Whales!!!" via YouTube.
  153. Smith, Tim D.; Reeves, Randall R.; Josephson, Elizabeth A.; Lund, Judith N. (27 April 2012). "Spatial and Seasonal Distribution of American Whaling and Whales in the Age of Sail". PLOS ONE. 7 (4): e34905. Bibcode:2012PLoSO...734905S. doi: 10.1371/journal.pone.0034905 . PMC   3338773 . PMID   22558102.
  154. JoongAng Ilbo. 2004. マッコウクジラ、90年ぶりに東海出現. Retrieved 17 August 2017
  155. Chang K.; Zhang C.; Park C.; Kang D.; Ju S.; Lee S.; Wimbush M., eds. (2015). Oceanography of the East Sea (Japan Sea). Springer International Publishing. p. 380. ISBN   9783319227207 . Retrieved 8 September 2015.
  156. "Sperm whales sighting off north-west Scotland 'extraordinary'". BBC News. 21 February 2013.
  157. Kasuya T., 2014, 鯨類研究50 年を顧みる, The Mammal Society of Japan
  158. "Something killed a lot of sperm whales in the past—and it wasn't whalers". 18 May 2018.
  159. 1 2 Whitehead, p. 79
  160. 1 2 Whitehead, pp. 43–55
  161. Smith S. & Whitehead, H. (2000). "The Diet of Galapagos sperm whales Physeter macrocephalus as indicated by faecal sample analysis". Marine Mammal Science. 16 (2): 315–325. Bibcode:2000MMamS..16..315S. doi:10.1111/j.1748-7692.2000.tb00927.x.
  162. Perkins, S. (23 February 2010). "Sperm Whales Use Teamwork to Hunt Prey". Wired. Retrieved 24 February 2010.
  163. Clapham, Philip J. (November–December 2011). "Mr. Melville's Whale". American Scientist. 6. 99 (6): 505–506. doi:10.1511/2011.93.505.
  164. Gaskin D. & Cawthorn M. (1966). "Diet and feeding habits of the sperm whale (Physeter macrocephalus L.) in the Cook Strait region of New Zealand". New Zealand Journal of Marine and Freshwater Research. 1 (2): 156–179. doi: 10.1080/00288330.1967.9515201 .
  165. 1 2 "Sneaky Cetaceans". Arctic Science Journeys. Retrieved 4 November 2008.
  166. "Whale Buffet". Archived from the original on 7 February 2007. Retrieved 19 March 2007.
  167. "FLMNH Ichthyology Department: Megamouth". Flmnh.ufl.edu. Retrieved 23 June 2012.
  168. Compagno, L. J. V. (2001). Sharks of the World Volume 2 Bullhead, mackerel and carpet sharks (PDF). FAO Species Catalogue for Fishery Purposes. pp. 74–78.[ permanent dead link ]
  169. Clarke, M.R.; Martins, H.R.; Pascoe, P. (29 January 1993). "The diet of sperm whales (Physeter macrocephalus Linnaeus 1758) off the Azores". Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. 339 (1287): 67–82. Bibcode:1993RSPTB.339...67C. doi:10.1098/rstb.1993.0005. PMID   8096086.
  170. Best, P. B. (June 1999). "Food and feeding of sperm whales Physeter macrocephalus off the west coast of South Africa". South African Journal of Marine Science. 21 (1): 393–413. doi: 10.2989/025776199784126033 .
  171. 1 2 3 Chua, Marcus A.H.; Lane, David J.W.; Ooi, Seng Keat; Tay, Serene H.X.; Kubodera, Tsunemi (5 April 2019). "Diet and mitochondrial DNA haplotype of a sperm whale (Physeter macrocephalus) found dead off Jurong Island, Singapore". PeerJ. 7: e6705. doi: 10.7717/peerj.6705 . PMC   6452849 . PMID   30984481.
  172. Dannenfeldt K.H. (1982). "Ambergris: The Search for Its Origin". Isis. 73 (3): 382–397. doi:10.1086/353040. PMID   6757176. S2CID   30323379.
  173. "Sperm Whales". North American Oceanic and Atmospheric Administration. 30 January 2023.
  174. Whitehead H. & Shin M. (2022). "Current global population size, post-whaling trend and historical trajectory of sperm whales". Scientific Reports. 12 (1): 19468. Bibcode:2022NatSR..1219468W. doi: 10.1038/s41598-022-24107-7 . PMC   9663694 . PMID   36376385.
  175. The State of World Fisheries and Aquaculture. Food and Agriculture Organization of the United Nations. 2022. doi:10.4060/cc0461en. hdl:10535/3776. ISBN   978-92-5-136364-5.
  176. Benoit-Bird K. Au W. & Kastelein R. (August 2006). "Testing the odontocete acoustic prey debilitation hypothesis: No stunning results". The Journal of the Acoustical Society of America. 120 (2): 1118–1123. Bibcode:2006ASAJ..120.1118B. doi:10.1121/1.2211508. PMID   16938998.
  177. Fais, A.; Johnson, M.; Wilson, M.; Aguilar Soto, N.; Madsen, P.T. (2016). "Sperm whale predator-prey interactions involve chasing and buzzing, but no acoustic stunning". Scientific Reports. 6: 28562. Bibcode:2016NatSR...628562F. doi:10.1038/srep28562. PMC   4919788 . PMID   27340122.
  178. Channel 4 British television program Jimmy and the Whale Whisperer, Sunday 23 September 2012, 7 pm to 8 pm
  179. Lavery, T. J.; Roudnew, B.; Gill, P.; Seymour, J.; Seuront, L.; Johnson, G.; Mitchell, J. G.; Smetacek, V. (2010). "Iron defecation by sperm whales stimulates carbon export in the Southern Ocean". Proceedings of the Royal Society B: Biological Sciences. 277 (1699): 3527–3531. doi:10.1098/rspb.2010.0863. PMC   2982231 . PMID   20554546.
  180. Whitehead, p. 276
  181. Ellis, Richard (2011). The Great Sperm Whale: A Natural History of the Ocean's Most Magnificent and Mysterious Creature. Zoology. Vol. 179. USA: University Press of Kansas. p.  146. ISBN   978-0-7006-1772-2. Zbl   0945.14001.
  182. Whitehead, p. 343
  183. 1 2 Whitehead, p. 122
  184. Whitehead, p. 123
  185. Whitehead, p. 185
  186. 1 2 Mammals in the Seas Vol. 3: General Papers & Large Cetaceans (Fao/Unep). Food & Agriculture Org. 1981. p. 499. ISBN   978-92-5-100513-2.
  187. General Whale Information. Biology.kenyon.edu. Retrieved 2013-03-19.
  188. Whale Milk. Whalefacts.org. Retrieved 2013-03-19.
  189. Milk Calorie Counter. Calorielab.com. Retrieved 2013-03-19.
  190. Whitehead, p. 232
  191. Whitehead, p. 233
  192. Whitehead, p. 235
  193. Whitehead, p. 204
  194. Perkins, Sid (23 February 2010). "Sperm Whales Use Teamwork to Hunt Prey". WIRED.
  195. "National Marine Mammal Laboratory". 27 January 2021.
  196. Pitman RL, Ballance LT, Mesnick SI, Chivers SJ (2001). "Killer whale predation on sperm whales: Observations and implications". Marine Mammal Science. 17 (3): 494–507. Bibcode:2001MMamS..17..494P. doi:10.1111/j.1748-7692.2001.tb01000.x. Archived from the original on 5 June 2013.
  197. Whitehead, H. & Weilgart, L. (2000). "The Sperm Whale". In Mann, J.; Connor, R.; Tyack, P. & Whitehead, H. (eds.). Cetacean Societies. The University of Chicago Press. p.  165. ISBN   978-0-226-50341-7.
  198. "Orcas vs Sperm Whales". Blue Sphere Media. Retrieved 20 November 2019.
  199. 1 2 Ponnampalam S.L., 2016, No Danger in Sight? An Observation of Sperm Whales (Physeter macrocephalus) in Marguerite Formation off Muscat, Sultanate of Oman
  200. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
  201. Melville, Herman (1985). Moby Dick; Or the Whale. London: Chancellor. p. 405. ISBN   978-1851520114.
  202. Jefferson, T. A., Stacey, P. J., & Baird, R. W. (1991). A review of killer whale interactions with other marine mammals: Predation to co‐existence. Mammal review, 21(4), 151–180.
  203. Pitman, R. L., Ballance, L. T., Mesnick, S. I., & Chivers, S. J. (2001). Killer whale predation on sperm whales: observations and implications. Marine mammal science, 17(3), 494–507.
  204. Estes, J. (2006). Whales, Whaling, and Ocean Ecosystems. University of California Press. p. 179. ISBN   978-0-520-24884-7 . Retrieved 3 November 2008.
  205. Kurita T., 2010, 『シャチに襲われたマッコウクジラの行動』, Japan Cetology Research Group News Letter 25. Retrieved 10-05-2014
  206. 1 2 Whitehead, H. (2003). Sperm whales: social evolution in the ocean. University of Chicago press.
  207. Martinez, D. R., & Klinghammer, E. (1970). The Behavior of the Whale Orcinus orca: a Review of the Literature. Zeitschrift für Tierpsychologie, 27(7), 828–839.
  208. C. Howard, Brian (2013). ""Astonishing" and Rare Orca vs. Sperm Whales Video Explained". National Geographic: Voices, Ocean News. Archived from the original on 22 December 2015. Retrieved 12 December 2015.
  209. Purves, M. G., Agnew, D. J., Balguerias, E., Moreno, C. A., & Watkins, B. (2004). "Killer whale (Orcinus orca) and sperm whale (Physeter macrocephalus) interactions with longline vessels in the Patagonian toothfish fishery at South Georgia, South Atlantic". Ccamlr Science, 11(111–126).
  210. Poon, Linda (23 January 2013). "Deformed Dolphin Accepted into New Family". National Geographic News. Archived from the original on 25 January 2013. Retrieved 8 February 2013.
  211. Shiretoko Nature Cruise Archived 30 May 2014 at the Wayback Machine . 2008. Shiretoko Rausu-cho Tourist Association. Retrieved 13-05-2014
  212. Weller, David W.; Würsig, Bernd; Whitehead, Hal; Norris, Jeffrey C.; Lynn, Spencer K.; Davis, Randall W.; Clauss, Nathalie; Brown, Patricia (October 1996). "OBSERVATIONS OF AN INTERACTION BETWEEN SPERM WHALES AND SHORT-FINNED PILOT WHALES IN THE GULF OF MEXICO". Marine Mammal Science. 12 (4): 588–594. Bibcode:1996MMamS..12..588W. doi:10.1111/j.1748-7692.1996.tb00071.x.
  213. Shiretoko Nature Cruise Archived 12 May 2014 at the Wayback Machine . 2008.
  214. Dailey, Murray; Vogelbein, Wolfgang (1991). "Parasite Fauna of 3 Species of Antarctic Whales With Reference To Their Use As Potential Stock Indicators" (PDF). Fishery Bulletin. 89 (3): 355–365. Retrieved 10 March 2021.
  215. 1 2 3 Nikaido, M.; Matsuno, F.; Hamilton, H.; Brownwell, R.; Cao, Y.; Ding, W.; Zuoyan, Z.; Shedlock, A.; Fordyce, R. E.; Hasegawa, M. & Okada, N. (19 June 2001). "Retroposon analysis of major cetacean lineages: The monophyly of toothed whales and the paraphyly of river dolphins". Proceedings of the National Academy of Sciences of the United States of America. 98 (13): 7384–7389. Bibcode:2001PNAS...98.7384N. doi: 10.1073/pnas.121139198 . PMC   34678 . PMID   11416211.
  216. 1 2 3 4 Bianucci, G. & Landini, W. (8 September 2006). "Killer sperm whale: a new basal physeteroid (Mammalia, Cetacea) from the Late Miocene of Italy". Zoological Journal of the Linnean Society. 148 (1): 103–131. doi: 10.1111/j.1096-3642.2006.00228.x .
  217. 1 2 Fordyce, R. E. & Barnes, L. G. (May 1994). "The Evolutionary History of Whales and Dolphins" (PDF). Annual Review of Earth and Planetary Sciences. 22 (1): 419–455. Bibcode:1994AREPS..22..419F. doi:10.1146/annurev.ea.22.050194.002223. Archived from the original (PDF) on 20 July 2011. Retrieved 4 October 2008.
  218. Stucky, R.E. & McKenna, M.C. (1993). "Mammalia". In Benton, M.J. (ed.). The Fossil Record . London: Chapman & Hall. pp.  739–771. ISBN   9780412393808.
  219. 1 2 3 4 5 6 7 Mchedlidze, G. "Sperm whales, evolution", pp. 1172–1174 in Perrin
  220. 1 2 Hirota, K. & Barnes, L. G. (5 April 2006). "A new species of Middle Miocene sperm whale of the genus Scaldicetus (Cetacea; Physeteridae) from Shiga-mura, Japan". Island Arc. 3 (4): 453–472. doi:10.1111/j.1440-1738.1994.tb00125.x.
  221. Bianucci, G.; Landrini, W. & Varola, W. (September–October 2004). "First discovery of the Miocene northern Atlantic sperm whale Orycterocetus in the Mediterranean". Geobios. 37 (5): 569–573. Bibcode:2004Geobi..37..569B. doi:10.1016/j.geobios.2003.05.004.
  222. "Physeter antiquus (Gervais 1849)". The Paleobiology Database.
  223. "Physeter vetus (Leidy 1849)". The Paleobiology Database.
  224. Hay, Oliver Perry (1923). The Pleistocene of North America and Its Vertebrated Animals from the States East of the Mississippi River and from the Canadian Provinces East of Longitude 95. Carnegie Institution of Washington. p. 370. ISBN   9780598344724.
  225. 1 2 Whitehead, pp. 2–3
  226. Heyning, J. (23 August 2006). "Sperm Whale Phylogeny Revisited: Analysis of the Morphological Evidence". Marine Mammal Science. 13 (4): 596–613. doi:10.1111/j.1748-7692.1997.tb00086.x.
  227. Wilson, D. (1999). The Smithsonian Book of North American Mammals. Vancouver: UBC Press. p. 300. ISBN   978-0-7748-0762-3.
  228. The Southampton Oceanography Centre & A deFontaubert. "The status of natural resources on the high seas" (PDF). IUCN. p. 63. Retrieved 11 October 2008.
  229. Jamieson, A. (1829). A Dictionary of Mechanical Science, Arts, Manufactures, and Miscellaneous Knowledge. H. Fisher, Son & Co. p.  566.
  230. "Aquarium of the Pacific – Sperm Whale". Archived from the original on 14 March 2019. Retrieved 11 October 2008.
  231. Whitehead, p. 14
  232. Simons, B. "Christopher Hussey Blown Out (Up) to Sea". Nantucket Historical Association.
  233. Dudley, P. (1725). "An Essay upon the Natural History of Whales, with a Particular Account of the Ambergris Found in the Sperma Ceti Whale". Philosophical Transactions (1683–1775), Vol. 33. The Royal Society. p. 267.
  234. 1 2 Dolin, E. (2007). Leviathan: The History of Whaling in America. W. W. Norton. pp.  98–100. ISBN   978-0-393-06057-7.
  235. Starbuck, A. (1878). History of the American Whale Fishery from its Earliest Inception to the Year 1876. ISBN   978-0-665-35343-7.
  236. 1 2 3 Bockstoce, J. (December 1984). "From Davis Strait to Bering Strait: The Arrival of the Commercial Whaling Fleet in North America's West Arctic" (PDF). Arctic. 37 (4): 528–532. doi:10.14430/arctic2234. Archived from the original (PDF) on 3 March 2016. Retrieved 15 October 2008.
  237. Estes, J. (2006). Whales, Whaling, and Ocean Ecosystems . University of California Press. p.  329. ISBN   978-0-520-24884-7.
  238. 1 2 Whitehead, pp. 13–21
  239. Stackpole, E. A. (1972). Whales & Destiny: The Rivalry between America, France, and Britain for Control of the Southern Whale Fishery, 1785–1825. The University of Massachusetts Press. ISBN   978-0-87023-104-9.
  240. Baldwin, R.; Gallagher, M. & van Waerebeek, K. "A Review of Cetaceans from Waters off the Arabian Peninsula" (PDF). p. 6. Retrieved 15 October 2008.
  241. "The Wreck of the Whaleship Essex". BBC. Retrieved 11 October 2008.
  242. Davis, L; Gallman, R. & Gleiter, K. (1997). In Pursuit of Leviathan: Technology, Institutions, Productivity, and Profits in American Whaling, 1816–1906 (National Bureau of Economic Research Series on Long-Term Factors in Economic Dev). University of Chicago Press. p. 135. ISBN   978-0-226-13789-6.
  243. Over 680,000 officially reported at "Whaling Statistics". Archived from the original on 15 October 2019. Retrieved 15 October 2008.. In addition, studies have found that official reports understated USSR catches by at least 89,000 "Sperm Whale (Physeter macrocephalus) California/Oregon/Washington Stock" (PDF). Retrieved 16 October 2008. Furthermore, other countries, such as Japan, have been found to have understated catches. "The RMS – A Question of Confidence: Manipulations and Falsifications in Whaling" (PDF). Archived from the original (PDF) on 7 October 2008. Retrieved 16 October 2008.
  244. Lavery, Trish L.; Ben Roudnew; Peter Gill; Justin Seymour; Laurent Seuront; Genevieve Johnson; James G. Mitchell & Victor Smetacek (2010). "Iron defecation by sperm whales stimulates carbon export in the Southern Ocean". Proceedings of the Royal Society B . 277 (1699): 3527–3531. doi:10.1098/rspb.2010.0863. PMC   2982231 . PMID   20554546.
  245. Whitehead, pp. 360–362
  246. Whitehead, pp. 362–368
  247. "Sperm whale (Physeter catodon) species profile". Environmental Conservation Online System. United States Fish and Wildlife Service. 16 November 2010.
  248. 1 2 3 4 "Appendix I and Appendix II" of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). As amended by the Conference of the Parties in 1985, 1988, 1991, 1994, 1997, 1999, 2002, 2005 and 2008. Effective: 5 March 2009.
  249. "Museum of New Zealand Te Papa Tongarewa Collections Online Search – Rei puta". Archived from the original on 4 November 2012.
  250. Arno, A. (2005). "Cobo and tabua in Fiji: Two forms of cultural currency in an economy of sentiment". American Ethnologist. 32 (1): 46–62. doi:10.1525/ae.2005.32.1.46. INIST   16581746.
  251. Ratzel, Friedrich (1896). "Dress and Weapons of the Melanesians: Ornament", The History of Mankind. London: MacMillan. Retrieved 21 October 2009.
  252. Constantine, R. "Folklore and Legends", p. 449 in Perrin
  253. Van Doren, Carl (1921). "Chapter 3. Romances of Adventure. Section 2. Herman Melville". The American Novel. Bartleby.com. Retrieved 19 October 2008.
  254. 1 2 Zwart, H. (2000). "What is a Whale? Moby Dick, marine science and the sublime" (PDF). Erzählen und Moral. Narrativität Im Spannungsfeld von Ethik und Ästhetik. Tubingen Attempo: 185–214. Archived from the original (PDF) on 20 March 2009.
  255. Edwards, B. "The Playful Learnings" (PDF). Australasian Journal of American Studies. 25 (1): 1–13 (9). Archived from the original (PDF) on 20 July 2008.
  256. "Sperm whale designated Connecticut state animal," Cetacean Times, 1 (3) May 1975, p.6.
  257. "The State Animal". State of Connecticut Sites, Seals and Symbols. State of Connecticut. Archived from the original on 1 September 2011. Retrieved 26 December 2010. Reproduced from the Connecticut State Register & Manual.
  258. "Sperm whales". Whaletrips. 26 May 2016. Retrieved 11 December 2022.
  259. "Whale and dolphin watching in the Azores". Wildlife Extra. Retrieved 26 September 2008.
  260. "Whale Watching Dominica". Archived from the original on 27 January 2010. Retrieved 26 September 2008.
  261. "The Dominica Sperm Whale Project" . Retrieved 25 January 2016.
  262. "Whales are starving – their stomachs full of our plastic waste | Philip Hoare". The Guardian. 30 March 2016.
  263. "The Times-News - Google News Archive Search". news.google.com.
  264. Jacobsen, Jeff K.; Massey, Liam; Gulland, Frances (May 2010). "Fatal ingestion of floating net debris by two sperm whales (Physeter macrocephalus)". Marine Pollution Bulletin. 60 (5): 765–767. Bibcode:2010MarPB..60..765J. doi:10.1016/j.marpolbul.2010.03.008. PMID   20381092.

Further reading