Megalodon

The depiction of a shark's head by Nicolas Steno in his work The Head of a Shark Dissected

According to Renaissance accounts, gigantic triangular fossil teeth often found embedded in rocky formations were once believed to be the petrified tongues, or glossopetrae, of dragons and snakes. This interpretation was corrected in 1667 by Danish naturalist Nicolas Steno, who recognized them as shark teeth, and famously produced a depiction of a shark's head bearing such teeth. He described his findings in the book The Head of a Shark Dissected, which also contained an illustration of a megalodon tooth.[16][17][18]

Swiss naturalist Louis Agassiz gave this shark its initial scientific name, Carcharodon megalodon, in his 1843 work Recherches sur les poissons fossiles, based on tooth remains.[1][19] English paleontologist Edward Charlesworth in his 1837 paper used the name Carcharias megalodon, while citing Agassiz as the author, indicating that Agassiz described the species prior to 1843. English paleontologist Charles Davies Sherborn in 1928 listed an 1835 series of articles by Agassiz as the first scientific description of the shark.[20] The specific name megalodon translates to "big tooth", from Ancient Greek: μέγας, romanized: (mégas), lit. 'big, mighty' and ὀδούς (odoús), "tooth".[21][22] The teeth of megalodon are morphologically similar to those of the great white shark (Carcharodon carcharias), and on the basis of this observation, Agassiz assigned megalodon to the genus Carcharodon.[19]

There was one apparent description of the shark in 1881 classifying it as Selache manzonii.[23]

Diagram of the chronospecies evolution of megalodon

While the earliest megalodon remains have been reported from the Late Oligocene, around 28 million years ago (Mya),[24][25] there is disagreement as to when it appeared, with dates ranging to as young as 16 mya.[26] It has been thought that megalodon became extinct around the end of the Pliocene, about 2.6 Mya;[26][27] claims of Pleistocene megalodon teeth, younger than 2.6 million years old, are considered unreliable.[27] A 2019 assessment moves the extinction date back to earlier in the Pliocene, 3.6 Mya.[28]

Megalodon is now considered to be a member of the family Otodontidae, genus Otodus, as opposed to its previous classification into Lamnidae, genus Carcharodon.[26][12][27][6][7] Megalodon's classification into Carcharodon was due to dental similarity with the great white shark, but most authors currently believe that this is due to convergent evolution. In this model, the great white shark is more closely related to the extinct broad-toothed mako (Isurus hastalis) than to megalodon, as evidenced by more similar dentition in those two sharks; megalodon teeth have much finer serrations than great white shark teeth. The great white shark is more closely related to the mako shark (Isurus spp.), with a common ancestor around 4 Mya.[19][29] Proponents of the former model, wherein megalodon and the great white shark are more closely related, argue that the differences between their dentition are minute and obscure.[30]^: 23–25

Megalodon tooth with two great white shark teeth

The genus Carcharocles currently contains four species: C. auriculatus, C. angustidens, C. chubutensis, and C. megalodon.[31]^: 30–31 The evolution of this lineage is characterized by the increase of serrations, the widening of the crown, the development of a more triangular shape, and the disappearance of the lateral cusps.[31]^: 28–31[32] The evolution in tooth morphology reflects a shift in predation tactics from a tearing-grasping bite to a cutting bite, likely reflecting a shift in prey choice from fish to cetaceans.[33] Lateral cusplets were finally lost in a gradual process that took roughly 12 million years during the transition between C. chubutensis and C. megalodon.[33] The genus was proposed by D. S. Jordan and H. Hannibal in 1923 to contain C. auriculatus. In the 1980s, megalodon was assigned to Carcharocles.[19][31]^: 30 Before this, in 1960, the genus Procarcharodon was erected by French ichthyologist Edgard Casier, which included those four sharks and was considered separate from the great white shark. It is now considered a junior synonym of Carcharocles.[31]^: 30 The genus Palaeocarcharodon was erected alongside Procarcharodon to represent the beginning of the lineage, and, in the model wherein megalodon and the great white shark are closely related, their last common ancestor. It is believed to be an evolutionary dead-end and unrelated to the Carcharocles sharks by authors who reject that model.[30]^: 70

The great white shark (Carcharodon carcharias) and megalodon were previously thought to be close relatives.[19][29]

Another model of the evolution of this genus, also proposed by Casier in 1960, is that the direct ancestor of the Carcharocles is the shark Otodus obliquus, which lived from the Paleocene through the Miocene epochs, 60 to 13 Mya.[29][32] The genus Otodus is ultimately derived from Cretolamna, a shark from the Cretaceous period.[6][34] In this model, O. obliquus evolved into O. aksuaticus, which evolved into C. auriculatus, and then into C. angustidens, and then into C. chubutensis, and then finally into C. megalodon.

Another model of the evolution of Carcharocles, proposed in 2001 by paleontologist Michael Benton, is that the three other species are actually a single species of shark that gradually changed over time between the Paleocene and the Pliocene, making it a chronospecies.[31]^: 17[25][35] Some authors suggest that C. auriculatus, C. angustidens, and C. chubutensis should be classified as a single species in the genus Otodus, leaving C. megalodon the sole member of Carcharocles.[25][36]

The genus Carcharocles may be invalid, and the shark may actually belong in the genus Otodus, making it Otodus megalodon.[4] A 1974 study on Paleogene sharks by Henri Cappetta erected the subgenus Megaselachus, classifying the shark as Otodus (Megaselachus) megalodon, along with O. (M.) chubutensis. A 2006 review of Chondrichthyes elevated Megaselachus to genus, and classified the sharks as Megaselachus megalodon and M. chubutensis.[4] The discovery of fossils assigned to the genus Megalolamna in 2016 led to a re-evaluation of Otodus, which concluded that it is paraphyletic, that is, it consists of a last common ancestor but it does not include all of its descendants. The inclusion of the Carcharocles sharks in Otodus would make it monophyletic, with the sister clade being Megalolamna.[6]

The cladogram below represents the hypothetical relationships between megalodon and other sharks, including the great white shark. Modified from Shimada et al. (2016),[6] Ehret et al, (2009),[29] and the findings of Siversson et al. (2013).[37][38][39]

Restoration assuming a similarity in appearance to the great white shark

One interpretation on how megalodon appeared was that it was a robust-looking shark, and may have had a similar build to the great white shark. The jaws may have been blunter and wider than the great white, and the fins would have also been similar in shape, though thicker due to its size. It may have had a pig-eyed appearance, in that it had small, deep-set eyes.[40]

Another interpretation is that megalodon bore a similarity to the whale shark (Rhincodon typus) or the basking shark (Cetorhinus maximus). The tail fin would have been crescent-shaped, the anal fin and second dorsal fin would have been small, and there would have been a caudal keel present on either side of the tail fin (on the caudal peduncle). This build is common in other large aquatic animals, such as whales, tuna, and other sharks, in order to reduce drag while swimming. The head shape can vary between species as most of the drag-reducing adaptations are toward the tail-end of the animal.[31]^: 35–36

Sculpture in the Museum of Evolution in Puebla, Mexico

Since Carcharocles is derived from Otodus, and the two had teeth that bear a close similarity to those of the sand tiger shark (Carcharias taurus), megalodon may have had a build more similar to the sand tiger shark than to other sharks. This is unlikely since the sand tiger shark is a carangiform swimmer which requires faster movement of the tail for propulsion through the water than the great white shark, a thunniform swimmer.[31]^: 35–36[41]

Due to fragmentary remains, there have been many contradictory size estimates for megalodon, as they can only be drawn from fossil teeth and vertebrae.[42]^: 87[43] The great white shark has been the basis of reconstruction and size estimation, as it is regarded as the best analogue to megalodon. Several total length estimation methods have been produced from comparing megalodon teeth and vertebrae to those of the great white.[40][44][10][7]

Size comparison of the great white and whale shark to estimates for megalodon

Proportions of megalodon at lengths of 3 m (9.8 ft), 8 m (26 ft), and 16 m (52 ft), extrapolated from extant relatives, with a 1.65 m (5 ft 5 in) diver

Megalodon size estimates vary depending on the method used, with maximum total length estimates ranging from 14.2–20.3 meters (47–67 ft).[40][10][7] A 2015 study estimated the average total body length at 10.5 meters (34 ft), calculated from 544 megalodon teeth, found throughout geological time and geography, including adults and juveniles.[11][12] In comparison, large great white sharks are generally around 6 meters (20 ft) in length, with a few contentious reports suggesting larger sizes.[45][46][40] The whale shark is the largest living fish, with one large female reported with a precaudal length of 15 meters (49 ft) and an estimated total length of 18.8 meters (62 ft).[45][47] It is possible that different populations of megalodon around the globe had different body sizes and behaviors due to different ecological pressures.[12] Megalodon is thought to have been the largest macropredatory shark that ever lived.[40]

"A C. megalodon about 16 meters long would have weighed about 48 metric tons (53 tons). A 17-meter (56-foot) C. megalodon would have weighed about 59 metric tons (65 tons), and a 20.3-meter (67 foot) monster would have topped off at 103 metric tons (114 tons)."[13]

In his 2015 book, The Story of Life in 25 Fossils: Tales of Intrepid Fossil Hunters and the Wonders of Evolution, Donald Prothero proposed the body mass estimates for different individiuals of different length by extrapolating from a vertebral centra based on the dimensions of the great white,[13] a methodology also used for the 2008 study which supports the maximum mass estimate.[14]

In 2020, Cooper and his colleagues reconstructed a 2D model of megalodon based on the dimensions of all the extant lamnid sharks and suggested that a 16 meters (52 ft) long megalodon would have had a 4.65 m (15.3 ft) long head, 1.41 m (4 ft 8 in) tall gill slits, a 1.62 m (5 ft 4 in) tall dorsal fin, 3.08 m (10 ft 1 in) long pectoral fins, and a 3.85 m (12 ft 8 in) tall tail fin.[8] In 2022, Cooper and his colleagues also reconstructed a 3D model with the same basis as the 2020 study, resulting in a body mass estimate of 61.56 metric tons (67.86 short tons) for a 16 meters (52 ft) long megalodon (higher than the previous estimates); a vertebral column specimen named IRSNB P 9893 (formerly IRSNB 3121), belonging to a 46 year old individual from Belgium, was used for extrapolation. An individual of this size would have required 98,175 kcal per day, 20 times more than what the adult great white requires.[15]

Mature male megalodon may have had a body mass of 12.6 to 33.9 metric tons (13.9 to 37.4 short tons), and mature females may have been 27.4 to 59.4 metric tons (30.2 to 65.5 short tons), assuming that males could range in length from 10.5 to 14.3 meters (34 to 47 ft) and females 13.3 to 17 meters (44 to 56 ft).[40]

A 2015 study linking shark size and typical swimming speed estimated that megalodon would have typically swum at 18 kilometers per hour (11 mph)–assuming that its body mass was typically 48 metric tons (53 short tons)–which is consistent with other aquatic creatures of its size, such as the fin whale (Balaenoptera physalus) which typically cruises at speeds of 14.5 to 21.5 km/h (9.0 to 13.4 mph).[48] In 2022, Cooper and his colleagues converted this calculation into relative cruising speed (body lengths per second), resulting in an mean absolute crusing speed of 5 kilometers per hour (3.1 mph) and a mean relative cruising speed of 0.09 body lengths per second for a 16 meters (52 ft) long megalodon; the authors found their mean absolute cruising speed to be faster than any extant lamnid sharks and their mean relative cruising speed to be slower, consistent with previous estiamtes.[15]

Its large size may have been due to climatic factors and the abundance of large prey items, and it may have also been influenced by the evolution of regional endothermy (mesothermy) which would have increased its metabolic rate and swimming speed. The otodontid sharks have been considered to have been ectotherms, so on that basis megalodon would have been ectothermic. However, the largest contemporary ectothermic sharks, such as the whale shark, are filter feeders, while lamnids are now known to be regional endotherms, implying some metabolic correlations with a predatory lifestyle. These considerations, as well as tooth oxygen isotopic data and the need for higher burst swimming speeds in macropredators of endothermic prey than ectothermy would allow, imply that otodontids, including megalodon, were probably regional endotherms.[49]

In 2020, Shimada and colleagues suggested large size was instead due to intrauterine cannibalism, where the larger fetus eats the smaller fetus, resulting in progressively larger and larger fetuses, requiring the mother to attain even greater size as well as caloric requirements which would have promoted endothermy. Males would have needed to keep up with female size in order to still effectively copulate (which probably involved latching onto the female with claspers, like modern cartilaginous fish).[50]

The first attempt to reconstruct the jaw of megalodon was made by Bashford Dean in 1909, displayed at the American Museum of Natural History. From the dimensions of this jaw reconstruction, it was hypothesized that megalodon could have approached 30 meters (98 ft) in length. Dean had overestimated the size of the cartilage on both jaws, causing it to be too tall.[51][52]

Reconstruction by Bashford Dean in 1909

Tooth compared to hand

In 1973, John E. Randall, an ichthyologist, used the enamel height (the vertical distance of the blade from the base of the enamel portion of the tooth to its tip) to measure the length of the shark, yielding a maximum length of about 13 meters (43 ft).[53] However, tooth enamel height does not necessarily increase in proportion to the animal's total length.[30]^: 99

In 1994, marine biologists Patrick J. Schembri and Stephen Papson opined that O. megalodon may have approached a maximum of around 24 to 25 meters (79 to 82 ft) in total length.[54][55]

In 1996, shark researchers Michael D. Gottfried, Leonard Compagno, and S. Curtis Bowman proposed a linear relationship between the great white shark's total length and the height of the largest upper anterior tooth. The proposed relationship is: total length in meters = − (0.096) × [UA maximum height (mm)]-(0.22).[56][40] Using this tooth height regression equation, the authors estimated a total length of 15.9 meters (52 ft) based on a tooth 16.8 centimeters (6.6 in) tall, which the authors considered a conservative maximum estimate. They also compared the ratio between the tooth height and total length of large female great whites to the largest megalodon tooth. A 6-meter (20 ft) long female great white, which the authors considered the largest 'reasonably trustworthy' total length, produced an estimate of 16.8 meters (55 ft). However, based on the largest female great white reported, at 7.1 meters (23 ft), they estimated a maximum estimate of 20.2 meters (66 ft).[40]

In 2002, shark researcher Clifford Jeremiah proposed that total length was proportional to the root width of an upper anterior tooth. He claimed that for every 1 centimeter (0.39 in) of root width, there are approximately 1.4 meters (4.6 ft) of shark length. Jeremiah pointed out that the jaw perimeter of a shark is directly proportional to its total length, with the width of the roots of the largest teeth being a tool for estimating jaw perimeter. The largest tooth in Jeremiah's possession had a root width of about 12 centimeters (4.7 in), which yielded 16.5 meters (54 ft) in total length.[31]^: 88

In 2002, paleontologist Kenshu Shimada of DePaul University proposed a linear relationship between tooth crown height and total length after conducting anatomical analysis of several specimens, allowing any sized tooth to be used. Shimada stated that the previously proposed methods were based on a less-reliable evaluation of the dental homology between megalodon and the great white shark, and that the growth rate between the crown and root is not isometric, which he considered in his model. Using this model, the upper anterior tooth possessed by Gottfried and colleagues corresponded to a total length of 15 meters (49 ft).[57] Among several specimens found in the Gatún Formation of Panama, one upper lateral tooth was used by other researchers to obtain a total length estimate of 17.9 meters (59 ft) using this method.[36][58]

In 2019, Shimada revisited the size of megalodon and discouraged using non-anterior teeth for estimations, noting that the exact position of isolated non-anterior teeth is difficult to identify. Shimada provided maximum total length estimates using the largest anterior teeth available in museums. The tooth with the tallest crown height known to Shimada, NSM PV-19896, produced a total length estimate of 14.2 meters (47 ft). The tooth with the tallest total height, FMNH PF 11306, was reported at 16.8 centimeters (6.6 in). However, Shimada remeasured the tooth and found it actually to measure 16.2 centimeters (6.4 in). Using the total height tooth regression equation proposed by Gottfried and colleagues produced an estimate of 15.3 meters (50 ft).[7][10]

In 2021, Victor J. Perez, Ronny M. Leder, and Teddy Badaut proposed a method of estimating total length of megalodon from the sum of the tooth crown widths. Using more complete megalodon dentitions, they reconstructed the dental formula and then made comparisons to living sharks. The researchers noted that the 2002 Shimada crown height equations produce wildly varying results for different teeth belonging to the same shark (range of error of ± 9 metres (30 ft)), casting doubt on some of the conclusions of previous studies using that method. Using the largest tooth available to the authors, GHC 6, with a crown width of 13.3 centimeters (5.2 in), they estimated a maximum body length of approximately 20 meters (66 ft), with a range of error of approximately ± 3.5 metres (11 ft).[10] This maximum length estimate was also supported by Cooper and his colleagues in 2022.[15]

There are anecdotal reports of teeth larger than those found in museum collections.[7] Gordon Hubbell from Gainesville, Florida, possesses an upper anterior megalodon tooth whose maximum height is 18.4 centimeters (7.25 in), one of the largest known tooth specimens from the shark.[59] In addition, a 2.7-by-3.4-meter (9 by 11 ft) megalodon jaw reconstruction developed by fossil hunter Vito Bertucci contains a tooth whose maximum height is reportedly over 18 centimeters (7 in).[60]

Reconstruction showing the position of the replacement teeth

The most common fossils of megalodon are its teeth. Diagnostic characteristics include a triangular shape, robust structure, large size, fine serrations, a lack of lateral denticles, and a visible V-shaped neck (where the root meets the crown).[30]^: 55[36] The tooth met the jaw at a steep angle, similar to the great white shark. The tooth was anchored by connective tissue fibers, and the roughness of the base may have added to mechanical strength.[61] The lingual side of the tooth, the part facing the tongue, was convex; and the labial side, the other side of the tooth, was slightly convex or flat. The anterior teeth were almost perpendicular to the jaw and symmetrical, whereas the posterior teeth were slanted and asymmetrical.[62]

Megalodon teeth can measure over 180 millimeters (7.1 in) in slant height (diagonal length) and are the largest of any known shark species,[31]^: 33 implying it was the largest of all macropredatory sharks.[40] In 1989, a nearly complete set of megalodon teeth was discovered in Saitama, Japan. Another nearly complete associated megalodon dentition was excavated from the Yorktown Formations in the United States, and served as the basis of a jaw reconstruction of megalodon at the National Museum of Natural History (USNM). Based on these discoveries, an artificial dental formula was put together for megalodon in 1996.[30]^: 55[63]

The dental formula of megalodon is: 2.1.7.43.0.8.4. As evident from the formula, megalodon had four kinds of teeth in its jaws: anterior, intermediate, lateral, and posterior. Megalodon's intermediate tooth technically appears to be an upper anterior and is termed as "A3" because it is fairly symmetrical and does not point mesially (side of the tooth toward the midline of the jaws where the left and right jaws meet). Megalodon had a very robust dentition,[30]^: 20–21 and had over 250 teeth in its jaws, spanning 5 rows.[31]^: iv It is possible that large megalodon individuals had jaws spanning roughly 2 meters (6.6 ft) across.[31]^: 129 The teeth were also serrated, which would have improved efficiency in cutting through flesh or bone.[19][31]^: 1 The shark may have been able to open its mouth to a 75° angle, though a reconstruction at the USNM approximates a 100° angle.[40]

Reconstructed jaws on display at the National Aquarium in Baltimore

In 2008, a team of scientists led by S. Wroe conducted an experiment to determine the bite force of the great white shark, using a 2.5-meter (8.2 ft) long specimen, and then isometrically scaled the results for its maximum size and the conservative minimum and maximum body mass of megalodon. They placed the bite force of the latter between 108,514 to 182,201 newtons (24,395 to 40,960 lbf) in a posterior bite, compared to the 18,216 newtons (4,095 lbf) bite force for the largest confirmed great white shark, and 7,400 newtons (1,700 lbf) for the placoderm fish Dunkleosteus. In addition, Wroe and colleagues pointed out that sharks shake sideways while feeding, amplifying the force generated, which would probably have caused the total force experienced by prey to be higher than the estimate.[14][64]

In 2021, Antonio Ballell and Humberto Ferrón used Finite Element Analysis modeling to examine the stress distribution of three types of megalodon teeth and closely related mega-toothed species when exposed to anterior and lateral forces, the latter of which would be generated when a shark shakes its head to tear through flesh. The resulting simulations identified higher levels of stress in megalodon teeth under lateral force loads compared to its precursor species such as O. obliquus and O. angusteidens when tooth size was removed as a factor. This suggests that megalodon teeth were of a different functional significance than previously expected, challenging prior interpretations that megalodon's dental morphology was primarily driven by a dietary shift towards marine mammals. Instead, the authors proposed that it was a byproduct of an increase in body size caused by heterochronic selection.[65]

Reconstructed megalodon skeleton on display at the Calvert Marine Museum

Megalodon is represented in the fossil record by teeth, vertebral centra, and coprolites.[40][66] As with all sharks, the skeleton of megalodon was formed of cartilage rather than bone; consequently most fossil specimens are poorly preserved.[67] To support its large dentition, the jaws of megalodon would have been more massive, stouter, and more strongly developed than those of the great white, which possesses a comparatively gracile dentition. Its chondrocranium, the cartilaginous skull, would have had a blockier and more robust appearance than that of the great white. Its fins were proportional to its larger size.[40]

Some fossil vertebrae have been found. The most notable example is a partially preserved vertebral column of a single specimen, excavated in the Antwerp Basin, Belgium, in 1926. It comprises 150 vertebral centra, with the centra ranging from 55 millimeters (2.2 in) to 155 millimeters (6 in) in diameter. The shark's vertebrae may have gotten much bigger, and scrutiny of the specimen revealed that it had a higher vertebral count than specimens of any known shark, possibly over 200 centra; only the great white approached it.[40] Another partially preserved vertebral column of a megalodon was excavated from the Gram Formation in Denmark in 1983, which comprises 20 vertebral centra, with the centra ranging from 100 millimeters (4 in) to 230 millimeters (9 in) in diameter.[61]

Coprolite attributed to megalodon

The coprolite remains of megalodon are spiral-shaped, indicating that the shark may have had a spiral valve, a corkscrew-shaped portion of the lower intestines, similar to extant lamniform sharks. Miocene coprolite remains were discovered in Beaufort County, South Carolina, with one measuring 14 cm (5.5 in).[66]

Gottfried and colleagues reconstructed the entire skeleton of megalodon, which was later put on display at the Calvert Marine Museum in the United States and the Iziko South African Museum.[40][32] This reconstruction is 11.3 meters (37 ft) long and represents a mature male,[40]^: 61 based on the ontogenetic changes a great white shark experiences over the course of its life.[40]^: 65

Megalodon had a cosmopolitan distribution;[26][58] its fossils have been excavated from many parts of the world, including Europe, Africa, the Americas, and Australia.[30]^: 67[68] It most commonly occurred in subtropical to temperate latitudes.[26][30]^: 78 It has been found at latitudes up to 55° N; its inferred tolerated temperature range was 1–24 °C (34–75 °F).[note 1] It arguably had the capacity to endure such low temperatures due to mesothermy, the physiological capability of large sharks to maintain a higher body temperature than the surrounding water by conserving metabolic heat.[26]

Megalodon inhabited a wide range of marine environments (i.e., shallow coastal waters, areas of coastal upwelling, swampy coastal lagoons, sandy littorals, and offshore deep water environments), and exhibited a transient lifestyle. Adult megalodon were not abundant in shallow water environments, and mostly inhabited offshore areas. Megalodon may have moved between coastal and oceanic waters, particularly in different stages of its life cycle.[31]^: 33[70]

Fossil remains show a trend for specimens to be larger on average in the Southern Hemisphere than in the Northern, with mean lengths of 11.6 and 9.6 meters (38 and 31 ft), respectively; and also larger in the Pacific than the Atlantic, with mean lengths of 10.9 and 9.5 meters (36 and 31 ft) respectively. They do not suggest any trend of changing body size with absolute latitude, or of change in size over time (although the Carcharocles lineage in general is thought to display a trend of increasing size over time). The overall modal length has been estimated at 10.5 meters (34 ft), with the length distribution skewed towards larger individuals, suggesting an ecological or competitive advantage for larger body size.[12]

Megalodon had a global distribution and fossils of the shark have been found in many places around the world, bordering all oceans of the Neogene.[71]

Epoch	Formation	State	Continent
Pliocene	Luanda Formation	Angola	Africa
		Libya	Africa
		South Africa	Africa
	Castell'Arquato Formation	Italy	Europe
	Arenas de Huelva Formation	Spain	Europe
	Esbarrondadoiro Formation	Portugal	Europe
	Touril Complex Formation	Portugal	Europe
	Red Crag Formation	United Kingdom	Europe
	San Mateo Formation	United States	North America
	Towsley Formation	United States	North America
	Bone Valley Formation	United States	North America
	Tamiami Formation	United States	North America
	Yorktown Formation	United States	North America
	Highlands Formation	Antigua and Barbuda	North America
	Refugio Formation	Mexico	North America
	San Diego Formation	Mexico	North America
	Tirabuzon Formation	Mexico	North America
	Onzole Formation	Ecuador	South America
	Paraguaná Formation	Venezuela	South America
	Black Rock Sandstone	Australia	Oceania
	Cameron Inlet Formation	Australia	Oceania
	Grange Burn Formation	Australia	Oceania
	Loxton Sand Formation	Australia	Oceania
	Whaler's Bluff Formation	Australia	Oceania
	Tangahoe Formation	New Zealand	Oceania
Miocene
		Egypt	Africa
	Madagascar Basin	Madagascar	Africa
		Nigeria	Africa
	Varswater Formation	South Africa	Africa
	Baripada Limestone	India	Asia
	Arakida Formation	Japan	Asia
	Bihoku Group	Japan	Asia
	Fujina Formation	Japan	Asia
	Hannoura Formation	Japan	Asia
	Hongo Formation	Japan	Asia
	Horimatsu Formation	Japan	Asia
	Ichishi Formation	Japan	Asia
	Kurahara Formation	Japan	Asia
	Maenami Formation	Japan	Asia
	Matsuyama Group	Japan	Asia
	Sekinobana Formation	Japan	Asia
	Suso Formation	Japan	Asia
	Takakubo Formation	Japan	Asia
	Tonokita Formation	Japan	Asia
	Tsurushi Formation	Japan	Asia
	Wajimazaki Formation	Japan	Asia
	Yoshii Formation	Japan	Asia
		Myanmar	Asia
	Burgeschleinitz Formation	Austria	Europe
	Melker Sand Formation	Austria	Europe
	Rzehakia Formation	Austria	Europe
	Weissenegg Formation	Austria	Europe
	Antwerpen Sands Member	Belgium	Europe
		Cyprus	Europe
	Hrušky Formation	Czech Republic	Europe
	Gram Formation	Denmark	Europe
	Aquitaine Basin	France	Europe
		Germany	Europe
	Libano Sandstone	Italy	Europe
	Blue Clay Formation	Malta	Europe
	Globigerina Limestone[72]	Malta	Europe
	Aalten Member	Netherlands	Europe
	Breda Formation	Netherlands	Europe
	Korytnica Clays	Poland	Europe
	Leitha Limestone	Poland	Europe
	Esbarrondadoiro Formation	Portugal	Europe
	Filakovo Formation	Slovakia	Europe
	Arjona Formation	Spain	Europe
	Calcarenites of Sant Elm	Spain	Europe
		Turkey	Europe
	Monterey Formation	United States	North America
	Puente Formation	United States	North America
	Purisima Formation	United States	North America
	San Mateo Formation	United States	North America
	Santa Margarita Formation	United States	North America
	Temblor Formation	United States	North America
	Topanga Formation	United States	North America
	Bone Valley Formation	United States	North America
	Calvert Formation	United States	North America
	Kirkwood Formation	United States	North America
		Barbados	North America
	Cojímar Formation	Cuba	North America
	Kendance Formation	Grenada	North America
		Jamaica	North America
	Aymamón Limestone	Puerto Rico	North America
	Almejas Formation	Mexico	North America
	Carrillo Puerto Formation	Mexico	North America
	Chagres Formation	Panama	North America
Chucunaque Formation	Panama	North America
Gatún Formation	Panama	North America
Paraná Formation	Argentina	South America
Bahía Inglesa Formation	Chile	South America
Castilletes Formation	Colombia	South America
Miramar Formation	Peru	South America
Pisco Formation	Peru	South America
Camacho Formation	Uruguay	South America
Cantaure Formation	Venezuela	South America
Caujarao Formation	Venezuela	South America
Socorro Formation	Venezuela	South America
Urumaco Formation	Venezuela	South America
Batesford Limestone	Australia	Oceania
Black Rock Sandstone	Australia	Oceania
Gippsland Limestone	Australia	Oceania
Mannum Formation	Australia	Oceania
Morgan Limestone	Australia	Oceania
Port Campbell Limestone	Australia	Oceania
	Fiji	Oceania
	French Polynesia	Oceania
Duho Formation[73]	South Korea	Asia
Seogwipo Formation[74]	South Korea	Asia

Locations of megalodon fossil discoveries, yellow from the Pliocene and blue from the Miocene[26][71]

Vertebra of a whale bitten in half by a megalodon with visible gashes from teeth.

Though sharks are generally opportunistic feeders, megalodon's great size, high-speed swimming capability, and powerful jaws, coupled with an impressive feeding apparatus, made it an apex predator capable of consuming a broad spectrum of animals. Otodus megalodon was probably one of the most powerful predators to have existed.[15] A study focusing on calcium isotopes of extinct and extant elasmobranch sharks and rays revealed that megalodon fed at a higher trophic level than the contemporaneous great white shark ("higher up" in the food chain.)[75]

Fossil evidence indicates that megalodon preyed upon many cetacean species, such as dolphins, small whales, cetotheres, squalodontids (shark toothed dolphins), sperm whales, bowhead whales, and rorquals.[51][76][77] In addition to this, they also targeted seals, sirenians, and sea turtles.[70] The shark was an opportunist and piscivorous, and it would have also gone after smaller fish and other sharks.[51] Many whale bones have been found with deep gashes most likely made by their teeth.[30]^: 75 Various excavations have revealed megalodon teeth lying close to the chewed remains of whales,[30]^: 75[32] and sometimes in direct association with them.[78]

The feeding ecology of megalodon appears to have varied with age and between sites, like the modern great white shark. It is plausible that the adult megalodon population off the coast of Peru targeted primarily cetothere whales 2.5 to 7 meters (8.2 to 23 ft) in length and other prey smaller than itself, rather than large whales in the same size class as themselves.[76] Meanwhile, juveniles likely had a diet that consisted more of fish.[36][79]

Megalodon may have faced competition from macroraptorial sperm whales, such as Livyatan (above).[80]

Megalodon faced a highly competitive environment.[80] Its position at the top of the food chain[81] probably had a significant impact on the structuring of marine communities.[80][82] Fossil evidence indicates a correlation between megalodon and the emergence and diversification of cetaceans and other marine mammals.[30]^: 78[80] Juvenile megalodon preferred habitats where small cetaceans were abundant, and adult megalodon preferred habitats where large cetaceans were abundant. Such preferences may have developed shortly after they appeared in the Oligocene.[30]^: 74–75

Megalodon were contemporaneous with whale-eating toothed whales (particularly macroraptorial sperm whales and squalodontidae), which were also probably among the era's apex predators, and provided competition.[80] Some attained gigantic sizes, such as Livyatan, estimated between 13.5 to 17.5 meters (44 to 57 ft). Fossilized teeth of an undetermined species of such physeteroids from Lee Creek Mine, North Carolina, indicate it had a maximum body length of 8–10 m and a maximum lifespan of about 25 years. This is very different from similarly sized modern killer whales that live to 65 years, suggesting that unlike the latter, which are apex predators, these physeteroids were subject to predation from larger species such as megalodon or Livyatan.[83] By the Late Miocene, around 11 Mya, macroraptorials experienced a significant decline in abundance and diversity. Other species may have filled this niche in the Pliocene,[80][84] such as the fossil killer whale Orcinus citoniensis which may have been a pack predator and targeted prey larger than itself,[32][85][86][87] but this inference is disputed,[28] and it was probably a generalist predator rather than a marine mammal specialist.[88]

Megalodon may have subjected contemporaneous white sharks to competitive exclusion, as the fossil records indicate that other shark species avoided regions it inhabited by mainly keeping to the colder waters of the time.[89][30]^: 77 In areas where their ranges seemed to have overlapped, such as in Pliocene Baja California, it is possible that megalodon and the great white shark occupied the area at different times of the year while following different migratory prey.[30]^: 77[90] Megalodon probably also had a tendency for cannibalism, much like contemporary sharks.[91]

Artistic impression of a megalodon pursuing two Eobalaenoptera whales

Sharks often employ complex hunting strategies to engage large prey animals. Great white shark hunting strategies may be similar to how megalodon hunted its large prey.[92] Megalodon bite marks on whale fossils suggest that it employed different hunting strategies against large prey than the great white shark.[51]

One particular specimen–the remains of a 9-meter (30 ft) long undescribed Miocene baleen whale–provided the first opportunity to quantitatively analyze its attack behavior. Unlike great whites which target the underbelly of their prey, megalodon probably targeted the heart and lungs, with their thick teeth adapted for biting through tough bone, as indicated by bite marks inflicted to the rib cage and other tough bony areas on whale remains.[51] Furthermore, attack patterns could differ for prey of different sizes. Fossil remains of some small cetaceans, for example cetotheres, suggest that they were rammed with great force from below before being killed and eaten, based on compression fractures.[92]

There is also evidence that a possible separate hunting strategy existed for attacking raptorial sperm whales; a tooth belonging to an undetermined 4 m (13 ft) physeteroid closely resembling those of Acrophyseter discovered in the Nutrien Aurora Phosphate Mine in North Carolina suggests that a megalodon or O. chubutensis may have aimed for the head of the sperm whale in order to inflict a fatal bite, the resulting attack leaving distinctive bite marks on the tooth. While scavenging behavior cannot be ruled out as a possibility, the placement of the bite marks is more consistent with predatory attacks than feeding by scavenging, as the jaw is not a particularly nutritious area to for a shark feed or focus on. The fact that the bite marks were found on the tooth's roots further suggest that the shark broke the whale's jaw during the bite, suggesting the bite was extremely powerful. The fossil is also notable as it stands as the first known instance of an antagonistic interaction between a sperm whale and an otodontid shark recorded in the fossil record.[93]

During the Pliocene, larger cetaceans appeared.[94] Megalodon apparently further refined its hunting strategies to cope with these large whales. Numerous fossilized flipper bones and tail vertebrae of large whales from the Pliocene have been found with megalodon bite marks, which suggests that megalodon would immobilize a large whale before killing and feeding on it.[14][51]

Collection of teeth of juvenile megalodon and C. chubutensis from a probable nursery area in the Gatún Formation of Panama

In 2021, Shimada and colleagues calculated the growth rate of an approximately 9.2 m (30 ft) individual based on the Belgian vertebrate column specimen that presumably contains annual growth rings on three of its vertebrae. They estimated the individual died at 46 years of age, with a growth rate of 16 cm (6.3 in) per year, and a length of 2 m (6 ft 7 in) at birth. For a 15 m (49 ft) individual—which they considered to have been the maximum size attainable—this would equate to a lifespan of 88 to 100 years.[95] However, Cooper and his colleagues in 2022 estimated the length of this 46 year old individual at nearly 16 m (52 ft) based on the 3D reconstruction which resulted in the complete vertebral column to be 11.1 m (36 ft) long; the researchers claimed that this size estimate difference occurred due to the fact that Shimada and his colleagues extrapolated its size only based on the vertebral centra.[15]

Megalodon, like contemporaneous sharks, made use of nursery areas to birth their young in, specifically warm-water coastal environments with large amounts of food and protection from predators.[36] Nursery sites were identified in the Gatún Formation of Panama, the Calvert Formation of Maryland, Banco de Concepción in the Canary Islands,[96] and the Bone Valley Formation of Florida. Given that all extant lamniform sharks give birth to live young, this is believed to have been true of megalodon also.[97] Infant megalodons were around 3.5 meters (11 ft) at their smallest,[40]^: 61 and the pups were vulnerable to predation by other shark species, such as the great hammerhead shark (Sphyrna mokarran) and the snaggletooth shark (Hemipristis serra).[36] Their dietary preferences display an ontogenetic shift:[40]^: 65 Young megalodon commonly preyed on fish,[36] sea turtles,[70] dugongs,[31]^: 129 and small cetaceans; mature megalodon moved to off-shore areas and consumed large cetaceans.[30]^: 74–75

An exceptional case in the fossil record suggests that juvenile megalodon may have occasionally attacked much larger balaenopterid whales. Three tooth marks apparently from a 4-to-7-meter (13 to 23 ft) long Pliocene shark were found on a rib from an ancestral blue or humpback whale that showed evidence of subsequent healing, which is suspected to have been inflicted by a juvenile megalodon.[98][99]

The Earth experienced a number of changes during the time period megalodon existed which affected marine life. A cooling trend starting in the Oligocene 35 Mya ultimately led to glaciation at the poles. Geological events changed currents and precipitation; among these were the closure of the Central American Seaway and changes in the Tethys Ocean, contributing to the cooling of the oceans. The stalling of the Gulf Stream prevented nutrient-rich water from reaching major marine ecosystems, which may have negatively affected its food sources. The largest fluctuation of sea levels in the Cenozoic era occurred in the Plio-Pleistocene, between around 5 million to 12 thousand years ago, due to the expansion of glaciers at the poles, which negatively impacted coastal environments, and may have contributed to its extinction along with those of several other marine megafaunal species.[100] These oceanographic changes, in particular the sea level drops, may have restricted many of the suitable shallow warm-water nursery sites for megalodon, hindering reproduction.[101] Nursery areas are pivotal for the survival of many shark species, in part because they protect juveniles from predation.[102][36]

As its range did not apparently extend into colder waters, megalodon may not have been able to retain a significant amount of metabolic heat, so its range was restricted to shrinking warmer waters.[101][77][103] Fossil evidence confirms the absence of megalodon in regions around the world where water temperatures had significantly declined during the Pliocene.[30]^: 77 However, an analysis of the distribution of megalodon over time suggests that temperature change did not play a direct role in its extinction. Its distribution during the Miocene and Pliocene did not correlate with warming and cooling trends; while abundance and distribution declined during the Pliocene, megalodon did show a capacity to inhabit colder latitudes. It was found in locations with a mean temperature ranging from 12 to 27 °C (54 to 81 °F), with a total range of 1 to 33 °C (34 to 91 °F), indicating that the global extent of suitable habitat should not have been greatly affected by the temperature changes that occurred.[26] This is consistent with evidence that it was a mesotherm.[49]

Megalodon may have become coextinct with smaller baleen whale species, such as Piscobalaena nana.[104]

Marine mammals attained their greatest diversity during the Miocene,[30]^: 71 such as with baleen whales with over 20 recognized Miocene genera in comparison to only six extant genera.[105] Such diversity presented an ideal setting to support a super-predator such as megalodon.[30]^: 75 By the end of the Miocene, many species of mysticetes had gone extinct;[80] surviving species may have been faster swimmers and thus more elusive prey.[31]^: 46 Furthermore, after the closure of the Central American Seaway, tropical whales decreased in diversity and abundance.[103] The extinction of megalodon correlates with the decline of many small mysticete lineages, and it is possible that it was quite dependent on them as a food source.[76] Additionally, a marine megafauna extinction during the Pliocene was discovered to have eliminated 36% of all large marine species including 55% of marine mammals, 35% of seabirds, 9% of sharks, and 43% of sea turtles. The extinction was selective for endotherms and mesotherms relative to poikilotherms, implying causation by a decreased food supply[100] and thus consistent with megalodon being mesothermic.[49] Megalodon may have been too large to sustain itself on the declining marine food resources.[101] The cooling of the oceans during the Pliocene might have restricted the access of megalodon to the polar regions, depriving it of the large whales which had migrated there.[103]

Competition from large odontocetes, such as macropredatory sperm whales which appeared in the Miocene, and a member of genus Orcinus (i.e., Orcinus citoniensis) in the Pliocene,[80][84] is assumed to have contributed to the decline and extinction of megalodon.[26][31]^: 46–47[101][106] But this assumption is disputed:[28] The Orcininae emerged in Mid-Pliocene with O. citoniensis reported from the Pliocene of Italy,[84][107] and similar forms reported from the Pliocene of England and South Africa,[84] indicating the capacity of these dolphins to cope with increasingly prevalent cold water temperatures in high latitudes.[84] These dolphins were assumed to have been macrophagous in some studies,[26] but on closer inspection, these dolphins are not found to be macrophagous and fed on small fishes instead.[107] On the other hand, gigantic macropredatory sperm whales such as Livyatan-like forms are last reported from Australia and South Africa circa 5 million years ago.[108][109][110] Others, such as Hoplocetus and Scaldicetus also occupied a niche similar to that of modern killer whales but the last of these forms disappeared during the Pliocene.[111][107] Members of genus Orcinus became large and macrophagous in the Pleistocene.[107]

Paleontologist Robert Boessenecker and his colleagues rechecked the fossil record of megalodon for carbon dating errors and concluded that it disappeared circa 3.5 million years ago.[28] Boessenecker and his colleagues further suggest that megalodon suffered range fragmentation due to climatic shifts,[28] and competition with white sharks might have contributed to its decline and extinction.[28] Competition with white sharks is assumed to be a factor in other studies as well,[112][26][106] but this hypothesis warrants further testing.[113] Multiple compounding environmental and ecological factors including climate change and thermal limitations, collapse of prey populations and resource competition with white sharks are believed to have contributed to decline and extinction of megalodon for now.[106]

The extinction of megalodon set the stage for further changes in marine communities. The average body size of baleen whales increased significantly after its disappearance, although possibly due to other, climate-related, causes.[114] Conversely the increase in baleen whale size may have contributed to the extinction of megalodon, as they may have preferred to go after smaller whales; bite marks on large whale species may have come from scavenging sharks. Megalodon may have simply become coextinct with smaller whale species, such as Piscobalaena nana.[104] The extinction of megalodon had a positive impact on other apex predators of the time, such as the great white shark, in some cases spreading to regions where megalodon became absent.[26][112][115]