Temporal range: Tortonian
|Cast of skull at the Museo di storia naturale dell'Università di Pisa|
Lambert et al., 2010
(Lambert et al., 2010)
Livyatan is an extinct genus of sperm whale containing one species: L. melvillei. Its name was inspired by the biblical sea monster Leviathan, and the author of the book Moby-Dick, Herman Melville, where the antagonist is a large sperm whale. It was found in the Pisco Formation of Peru and lived during the Tortonian stage of the Miocene epoch, about 9.9-8.9 million years ago (mya), however a large tooth from Australia implies that either it or a close relative survived into the Pliocene, around 5 mya. It was a member of a group of hyper-predatory macroraptorial sperm whales (or "raptorial sperm whales") and was likely an apex predator preying on whales, seals, and so forth. Characteristic of raptorial sperm whales, Livyatan had functional, enamel-coated teeth on the upper and lower jaws, as well as several adaptations for hunting large prey.
Its total length was estimated to be around 13.5 or 17.5 m (44 or 57 ft), similar to the modern sperm whale (Physeter macrocephalus), making it one of the largest predators to have ever existed. The tallest tooth measured 36.2 cm (14.3 in), and is the largest tooth of any known animal. It is distinguished from the other raptorial sperm whales by the basin on the skull, and how it spans the entire length of the snout. The spermaceti organ, contained in that basin, is thought to have been used in biosonar and communication, or for ramming prey and other sperm whales. The whale may have interacted with the large extinct shark Megalodon (Carcharocles megalodon), competing with it for a similar food source. Its extinction was likely caused by climate change which resulted in a drop in food populations. The formations where the whale has been found have also preserved a large assemblage of marine life, such as sharks and marine mammals.
In November 2008, a partially preserved skull, as well as teeth and the lower jaw, belonging to L. melvillei, the holotype specimen MUSM 1676, were discovered in the coastal desert of Peru in the sediments of the Pisco Formation, 35 km (22 mi) southwest of the city of Ica. Klaas Post, a researcher for the Natuurhistorisch Museum Rotterdam in the Netherlands, stumbled across them on the final day of a field trip. The fossils were prepared in Lima, and are now part of the collection of the Natural History Museum there.
The discoverers originally assigned, in July 2010, the English name of the biblical monster, Leviathan, to the whale as Leviathan melvillei. However, the scientific name Leviathan was also the junior homonym for the mastodon (Mammut), so, in August 2010, the authors rectified this situation by coining a new genus name for the whale, Livyatan, from the original Hebrew name of the monster. The species name melvillei is a reference to Herman Melville, author of the book Moby-Dick, which features a gigantic sperm whale as the main antagonist. The first Livyatan fossils from Peru were dated to around 13-12 million years ago (mya) in the Serravallian Age of the Miocene, but this was revised to 9.9-8.9 mya in the Tortonian Age of the Miocene.
In 2016 in Beaumaris Bay, Australia, a large sperm whale tooth measuring 30 cm (12 in), specimen NMV P16205, was discovered in Pliocene strata by a local named Murray Orr, and was nicknamed the "Beaumaris sperm whale" or the "giant sperm whale". The tooth was donated to Museums Victoria at Melbourne. Though it has not been given a species designation, the tooth looks similar to those of L. melvillei, indicating that it was a close relative. The tooth is dated to around 5 mya, and so is younger than the Peruvian L. melvillei specimen by around 3 million years.
Livyatan was part of a fossil stem group of hyper-predatory sperm whales commonly known as macroraptorial sperm whales, or raptorial sperm whales, alongside the extinct whales Brygmophyseter, Acrophyseter, and Zygophyseter. This group is known for having large, functional teeth on both the upper and lower jaws, which were used in capturing large prey; and had an enamel coating. Conversely, the modern sperm whale (Physeter macrocephalus) lacks enamel, teeth in the upper jaw, and the ability to use its teeth to catch prey. Livyatan belongs to a different lineage than the other raptorial sperm whales, and the size increase and the development of the spermaceti organ, an organ that is characteristic of sperm whales, are thought to have evolved independently from other raptorial sperm whales. The large teeth of the raptorial sperm whales either evolved once in the group with a basilosaurid-like common ancestor, or independently in Livyatan. The large temporal fossa in the skull of raptorial sperm whales is thought to a plesiomorphic feature, that is, a trait inherited from a common ancestor. Since the teeth of fetal modern sperm whales (Physeter macrocephalus) have enamel on them before being coated with cementum, it is thought that the enamel is also an ancient characteristic (basal). The appearance of raptorial sperm whales in the fossil record coincides with the diversification of baleen whales in the Miocene, implying that they evolved specifically to exploit baleen whales. It has also been suggested that the raptorial sperm whales should be placed into the subfamily Hoplocetinae, alongside the genera Diaphorocetus, Idiorophus, Scaldicetus, and Hoplocetus, which are known from the Miocene to the lower Pliocene. This subfamily is characterized by their robust and enamel-coated teeth.
|Relationships between Livyatan and other sperm whales, raptorial sperm whales in bold|
Since only the skull of Livyatan is known, the ratio of the skull compared to the rest of the body length is unknown, and so its total body length is unclear. The total length of L. melvillei is estimated to have been around 13.5 m (44 ft) when using the modern sperm whale for scaling, and 16.2–17.5 m (53–57 ft) when using the raptorial Zygophyseter for scaling; scaling achieved by measuring the head-to-body ratios. In comparison, the modern sperm whale measures on average 11 to 16 m (36 to 52 ft), and the Beaumaris sperm whale was estimated to have been around 18 m (59 ft) and 40 t (44 short tons). The large size was probably an anti-predator adaptation, and allowed it to feed on larger prey. Livyatan is the largest fossil sperm whale discovered, and was also one of the biggest known predators, having one of the largest bites of any tetrapod and possibly of any vertebrate.
The holotype skull of Livyatan was 3 m (9.8 ft) long. Like other raptorial sperm whales, Livyatan had a wide gap in between the temporal fossae on the sides of the skull and the zygomatic processes on the front of the skull, indicating a large space for holding strong temporal muscles, which are the most powerful muscles between the skull and the jaw. The snout was robust, thick, and relatively small, which allowed it to clamp down harder and better handle struggling prey. The left and right premaxillae on the snout probably did not intersect at the tip of the snout, though the premaxillae took up most of the front end of the snout. Unlike in the modern sperm whale, the premaxillae reached the sides of the snout. The upper jaw was thick, especially midway through the snout. The snout was asymmetrical, with the right maxilla in the upper jaw becoming slightly convex towards the back of the snout, and the left maxilla becoming slightly concave towards the back of the snout. The vomer reached the tip of the snout, and was slightly concave, decreasing in thickness from the back to the front. A sudden thickening in the middle-left side of the vomer may indicate the location of the nose plug muscles. Each mandible in the lower jaw was higher than it was wide, with a larger gap in between the two than in the modern sperm whale. The mandibular symphysis which connects the two halves of the mandibles in the middle of the lower jaw was unfused. The condyloid process, which connects the lower jaw to the skull, was located near the bottom of the mandible like other sperm whales.
Unlike the modern sperm whale, Livyatan had functional teeth in both of its jaws. The wearing on the teeth indicates that the teeth sheared past each other while biting down, meaning it could bite off large portions of flesh from its prey. Also, the teeth were deeply embedded into the gums and could interlock, which were adaptations to holding struggling prey. None of the teeth of the holotype were complete, and none of the back teeth were well-preserved. The lower jaw contained 22 teeth, and the upper jaw contained 18 teeth. Unlike other sperm whales with functional teeth in the upper jaw, no tooth roots were entirely present in the premaxilla portion of the snout, and, consequently, its tooth count was lower than those sperm whales. Aside from the modern dwarf (Kogia sima) and pygmy (K. breviceps) sperm whales, it had the lowest tooth count in the lower jaw of any sperm whale.
The most robust teeth in L. melvillei were the fourth, fifth, and sixth teeth in each side of the jaw. The well-preserved teeth all had a height greater than 31 cm (12 in), and the largest teeth of the holotype were the second and third on the left lower jaw, which were calculated to be around 36.2 cm (14.3 in) high. The first right tooth was the smallest at around 31.5 cm (12.4 in). The Beaumaris sperm whale tooth measured around 30 cm (12 in) in length, and is the largest fossil tooth discovered in Australia. These teeth are thought to be among the largest of any known animal, excluding tusks; in comparison, the largest tooth specimen of Tyrannosaurus measured around 30.5 cm (12 in) in length, and the teeth of Megalodon (Carcharocles megalodon), a large extinct shark, were around 18 cm (7 in) long. Some of the lower teeth have been shown to contain a facet for when the jaws close, which may have been used to properly fit the largest teeth inside the jaw. In the front teeth, the tooth diameter decreased towards the base. This was the opposite for the back teeth, and the biggest diameters for these teeth were around 11.1 cm (4.4 in) in the lower jaw. All teeth featured a rapid shortening of the diameter towards the tip of the tooth, which were probably in part due to wearing throughout their lifetimes. The curvature of the teeth decreased from front to back, and the lower teeth were more curved at the tips than the upper teeth. The front teeth projected forward at a 45° angle, and, like in other sperm whales, cementum was probably continually added onto the teeth throughout its lifetime.
All tooth sockets were cylindrical and single-rooted. The tooth sockets increased in size from the first to the fourth and then decreased, the fourth being the largest at around 197 mm (7.8 in) in diameter in the upper jaws, which is the largest of any known whale species. The tooth sockets were smaller in the lower jaw than they were in the upper jaw, and they were circular in shape, except for the front sockets which were more ovular.
The fossil skull of Livyatan had a curved basin, known as the supracranial basin, which was deep and wide. Unlike other raptorial sperm whales, but much like in the modern sperm whale, the basin spanned the entire length of the snout, causing the entire skull to be concave on the top rather than creating a snout as seen in Zygophyseter and Acrophyseter. The supracranial basin was the deepest and widest over the braincase, and, unlike other raptorial sperm whales, it did not overhang the eye socket. It was defined by high walls on the sides. The antorbital notches, which are usually slit-like notches on the sides of the skull right before the snout, were inside the basin. A slanting crest on the temporal fossa directed towards the back of the skull separated the snout from the rest of the skull, and was defined by a groove starting at the antorbital processes on the cheekbones. The basin had two foramina in the front, as opposed to the modern sperm whale which has one foramen on the maxilla, and to the modern dwarf and pygmy sperm whales which have several in the basin. The suture in the basin between the maxilla and the forehead had an interlocking pattern.
Livyatan was an apex predator, and probably had a profound impact on the structuring of Miocene marine communities. Livyatan, using its large and deeply rooted teeth, is likely to have hunted large prey near the surface, and its diet probably mainly consisted of medium-sized baleen whales ranging from 7–10 m (20–30 ft) in length. It probably also preyed upon sharks, seals, dolphins, and other large marine vertebrates, occupying a niche similar to the modern killer whale (Orcinus orca). It was contemporaneous with and occupied the same region as Megalodon, which was likely also an apex predator, implying competition over their similar food source. It is assumed that the hunting tactics of Livyatan for hunting whales were similar to that of the modern killer whale, pursuing prey to wear it out, and then drowning it. Modern killer whales work in groups to isolate and kill whales, but, given its size, Livyatan may have been able to hunt alone.
The supracranial basin in its head suggests that Livyatan had a large spermaceti organ, a series of oil and wax reservoirs separated by connective tissue. The uses for the spermaceti organ in Livyatan are unknown. Much like in the modern sperm whale, it could have been used in the process of biosonar to generate sound for locating prey. It is possible that it was also used as a means of acoustic displays, such as for communication purposes between individuals. It may have been used for acoustic stunning, which would have caused the bodily functions of a target animal to shut down from exposure to the intense sounds.
Another theory says that the enlarged forehead caused by the presence of the spermaceti organ is used in all sperm whales between males fighting for females during mating season by head-butting each other, including Livyatan and the modern sperm whale. It may have also been used to ram into prey, if this is the case; in support of this, there have been two reports of modern sperm whales attacking whaling vessels by ramming into them, and the organ is disproportionally larger in male modern sperm whales.
An alternate theory is that sperm whales, including Livyatan, can alter the temperature of the wax in the organ to aid in buoyancy. Lowering the temperature increases the density to have it act as a weight for deep-sea diving, and raising the temperature decreases the density to have it pull the whale to the surface.
Livyatan is known from the Tortonian stage of the Upper Miocene 9.9-8.9 mya in the Pisco Formation of Peru, which is known for its well-preserved assemblage of marine vertebrates. The formation lies in the subduction zone between the Nazca Plate and the South American Plate, causing numerous pull-apart basins. Among the baleen whales found, the most common was an undescribed species of cetotheriid whale measuring around 5 to 8 m (16 to 26 ft), and most of the other baleen whales found were roughly the same size. Toothed whale remains found consist of beaked whales (such as Messapicetus gregarius), ancient pontoporiids (such as Brachydelphis mazeasi), oceanic dolphins, and the raptorial sperm whale Acrophyseter. All seal remains found represent the earless seals. Also found were large sea turtles such as Pacifichelys urbinai, which points to the development of seagrasses in this area. Partial bones of crocodiles were discovered. Of the seabirds, fragmentary bones of cormorants and petrels were discovered, as well as two species of boobies. The remains of many cartilaginous fish were discovered in this formation, including more than 3500 shark teeth, which mainly belonged to the ground sharks, such as requiem sharks and hammerhead sharks. To a lesser extent, mackerel sharks were also found, such as white sharks, sand sharks, and Otodontidae. Many shark teeth were associated with the extinct broad-tooth mako (Cosmopolitodus/Carcharodon hastalis) and Megalodon, and the teeth of these two sharks were found near whale and seal remains. Eagle rays, sawfish, and angelsharks were other cartilaginous fish found. Most of the bony fish findings belonged to tunas and croakers. Livyatan and Megalodon were likely the apex predators of this area during this time.
The Beaumaris sperm whale was found in the Beaumaris Bay Black Rock Sandstone Formation in Australia near the city of Melbourne, dating to 5 mya in the Pliocene. Beaumaris Bay is one of the most productive marine fossil sites in Australia for marine megafauna. Shark teeth belonging to twenty different species have been discovered there, such as from the whale shark (Rhincodon typus), the Port Jackson shark (Heterodontus portusjacksoni), the broad-toothed mako, and Megalodon. Some examples of whales found include the ancient humpback whale Megaptera miocaena, the dolphin Steno cudmorei, and the sperm whale Physetodon baileyi. Other large marine animals found include ancient elephant seals, dugongs, sea turtles, ancient penguins such as Pseudaptenodytes, the extinct albatross Diomedea thyridata, and the extinct toothed seabirds of the genus Pelagornis.
A cooling event at the end of the Miocene, which caused baleen whales to increase in size and decrease in diversity, may have been the cause of the extinction of Livyatan, becoming coextinct with the small baleen whales it fed on. An alternate, though less likely, theory is that it became too big to effectively hunt the smaller creatures it depended on.
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|Wikispecies has information related to L. melvillei|
|Wikimedia Commons has media related to L. melvillei.|
- 'Sea monster' fossil found in Peru desert by CNN
- Ancient sperm whale's giant head uncovered from Los Angeles Times (The skull is on display in National History Museum in Lima)
- A killer sperm whale with details on sperm whale evolution