Temporal range: Late Eocene
|B. cetoides, National Museum of Natural History, Washington D.C.|
Basilosaurus ("king lizard") is a genus of early whale that lived in the late Eocene. The first fossil of B. cetoides was discovered in the United States and was initially believed to be some sort of reptile, hence the suffix -"saurus", but it was later found to be a marine mammal. Richard Owen wished to rename the creature Zeuglodon ("yoked tooth"), but, per taxonomic rules, the creature's first name remained permanent. Fossils of B. isis have been found in Egypt and Jordan.
The dental formula for Basilosaurus isis is 22.214.171.124. The upper and lower molars and second to fourth premolars are double rooted and high-crowned.
The head of Basilosaurus did not have room for a melon like modern day toothed whales, and the brain was smaller in comparison as well. It is believed that they therefore did not have the social capabilities of modern whales.
Fahlke et al. 2011 concluded that the skull of Basilosaurus is asymmetrical like in modern toothed whales, and not, as previously assumed, symmetrical like in baleen whales and artiodactyls closely related to cetaceans. In modern toothed whales this asymmetry is associated with high-frequency sound production and echolocation, neither of which is thought to be present in Basilosaurus. This cranial torsion probably evolved in protocetids and basilosaurids together with directional underwater hearing and the sound receiving apparatus in the mandible (the auditory fat pad and the pan bone (thin portion of mandible).)
In the basilosaur skull, the inner and middle ear are enclosed by a dense tympanic bulla. The synapomorphic cetacean air sinus system is partially present in basilosaurids, including the pterygoid, peribullary, maxillary, and frontal sinuses. The periotic bone, which surrounds the inner ear, is partially isolated. The mandibular canal is large and laterally flanked by a thin bony wall, the pan bone or acoustic fenestra. These features enabled basilosaurs to hear directionally in water.
The ear of basilosaurids is more derived than those in earlier archaeocetes, such as remingtonocetids and protocetids, in the acoustic isolation provided by the air-filled sinuses inserted between the ear and the skull. The basilosaurid ear did, however, have a large external auditory meatus, strongly reduced in modern cetaceans, but, even though this was probably functional, it can have been of little use under water.
A complete Basilosaurus skeleton was found in 2015, and several attempts have been made to reconstruct the vertebral column from partial skeletons. Kellogg 1936 estimated a total of 58 vertebrae, based on two partial and non-overlapping skeletons of B. cetoides from Alabama. More complete fossils uncovered in Egypt in the 1990s allowed a more accurate estimation: the vertebral column of B. isis has been reconstructed from three overlapping skeletons to a total of 70 vertebrae with a vertebral formula interpreted as 7 cervical, 18 thoracic, 20 lumbar and sacral, and 25 caudal vertebrae. It can be assumed that the vertebral formula of B. cetoides is the same.
Basilosaurus has an anguilliform (eel-like) body shape because of the elongation of the centra of the thoracic through anterior caudal vertebrae. In life, these vertebrae were filled with marrow, and, because of the enlarged size, this made them buoyant. From this it can be deduced that Basilosaurus swam predominantly in two dimensions at the sea surface, in contrast to the smaller Dorudon which was probably a diving, three-dimensional swimmer. The skeletal anatomy of the tail suggests that a small fluke was probably present, which would have aided only vertical motion. Most reconstructions show a small, speculative dorsal fin similar to a rorqual's, but other reconstructions show a dorsal ridge.
A 16 m (52 ft) individual of B. isis had 35 cm (14 in) long hindlimbs with fused tarsals and only three digits. The limited size of the limb and the absence of an articulation with the sacral vertebrae, makes a locomotory function unlikely. Analysis has shown that the reduced limbs could rapidly adduct between only two positions.
It is also believed[by whom?] that Basilosaurus relied on unusual modes of locomotion, relative to other cetaceans; similarly sized thoracic, lumbar, sacral and caudal vertebrae imply that it moved in an anguilliform (eel-like) fashion, but predominantly in the vertical plane. Paleontologist Philip D. Gingerich theorized that Basilosaurus may also have moved in a very odd, horizontal anguilliform fashion to some degree, something completely unknown in modern cetaceans.
The vertebrae appear to have been hollow, and it is likely that they were also fluid-filled. This would imply that Basilosaurus typically functioned in only two dimensions at the ocean surface, compared with the three-dimensional habits of most other cetaceans. Judging from the relatively weak axial musculature and the thick bones in the limbs, Basilosaurus is not believed to have been capable of sustained swimming or deep diving. It is also believed that it was incapable of terrestrial locomotion.
The cheek teeth of Basilosaurus retain a complex morphology and functional occlusion. Heavy wear on the teeth reveals that food was first chewed then swallowed. Scientists were able to estimate the bite force of Basilosaurus by analyzing the scarred up skull bones of another species of prehistoric whale, named Dorudon. By the damage caused, researchers calculated that the aquatic predator could chomp down with a skull crushing force of more than 1600 kilograms.
Analyses of the stomach contents of B. cetoides has shown that this species fed exclusively on fishes and sharks, while bite marks on the skulls of juvenile Dorudon have been matched with the dentition of B. isis, suggesting a dietary difference between the two species, similar to that found in different populations of modern killer whales.
During the early 19th century, Basilosaurus cetoides fossils were so common (and sufficiently large) that they were regularly used as furniture in the American south. Vertebrae were sent to the American Philosophical Society by a Judge Bry of Arkansas and Judge John Creagh of Clarke County, Alabama. Both fossils ended up in the hands of the anatomist Richard Harlan, who requested more examples from Creagh. The first bones were unearthed when rain caused a hill side full of sea shells to slide. The bones were lying in a curved line "measuring upwards of four hundred feet in length, with intervals which were vacant." Many of these bones were used as andirons and destroyed; Bry saved the bones he could find but was convinced more bones were still to be found on the location. Bry speculated that the bones must have belonged to a "sea monster" and supplied "a piece having the appearance of a tooth" to help determine which kind.
Harlan identified the tooth as a wedge-shaped shell and instead focused on "a vertebra of enormous dimensions" which he assumed belonged to the order "Enalio-Sauri of Conybeare", "found only in the sub-cretaceous series." He noted that some parts of the vertebra were similar to those of Plesiosaurus, but that they were completely different in proportions. Comparing his vertebra to those of large dinosaurs such as Megalosaurus and Iguanodon, Harlan concluded that his specimen was considerably larger — he estimated the animal to have been "no less" than 80–100 ft (24–30 m) long — and therefore suggested the name Basilosaurus, meaning “king lizard”.
Harlan brought his assembled specimens (including fragments of jaw and teeth, humerus, and fragments of rib) to the UK where he presented them to anatomist Richard Owen. Owen concluded that the molar teeth were two-rooted, a dental morphology unknown in fishes and reptiles, and more complex and varied than in any known reptile, and therefore that the specimen must be a mammal. Owen correctly associated the teeth with cetaceans, but erroneously with "herbivorous cetaceans" (all cetaceans are carnivorous) such as the dugong (a sirenian, not a cetacean). Consequently, Owen proposed renaming the find Zeuglodon cetoides (“whale-like yoke teeth” in reference to the double-rooted teeth) and Harlan agreed. Zeuglodon, now a junior synonym, is considered by many to be a more fitting name, but the first-published name always takes precedence.
German botanist Georg August Schweinfurth discovered the first archaeocete whale in Egypt (Zeuglodon osiris, now Saghacetus osiris) in 1879. He visited the Qasr el Sagha Formation in 1884 and 1886 and missed the now famous Zeuglodon Valley with a few kilometers. German paleontologist Wilhelm Barnim Dames described the material, including the type specimen of Z. osiris, a well-preserved dentary. 
Hugh Beadnell, head of the Geological Survey of Egypt 1896–1906, named and described Zeuglodon isis in Andrews 1904 based on a partial mandible and several vertebrae from Wadi Al-Hitan in Egypt. Andrews 1906 described a skull and some vertebrae of a smaller archaeocete and named it Prozeuglodon atrox (=Dorudon atrox). Kellogg 1936 discovered deciduous teeth in this skull and it was then believed to be a juvenile [Pro]zeuglodon isis for decades before more complete fossils of mature Dorudon were discovered.
In the 1980s, Elwyn L. Simons and Philip D. Gingerich started to excavate at Qasr el-Sagha and Wadi Al-Hitan with the hope of finding material that could match archaeocete fossils from Pakistan. Since then over 500 archaeocete skeletons have been found at these two locations, of which most are B. isis or D. atrox, several of the latter carrying bite marks assumed to be from the former.  Gingerich, Smith & Simons 1990 described additional fossils including foot bones and speculated that the reduced hindlimbs were used as copulatory guides.
- Zeuglodon wanklyni was described in 1876 based on a skull found in the Wanklyn's Barton Cliff in the United Kingdom. This single specimen, however, quickly disappeared and has since been declared a nomen nudum or referred to as Zygorhiza wanklyni.
- Zeuglodon vredense or vredensis was named in the 19th century based on a single, isolated tooth without any kind of accompanying description, and Kellogg 1936 therefore declared it a nomen nudum.
- Zeuglodon puschi[i] from Poland was named by Brandt 1873. Kellogg 1936 noted that the species is based on an incomplete vertebra of indeterminable position and, therefore, that the species is invalid.
- Zeuglodon brachyspondylus was described by Müller 1849 based on some vertebrae from Zeuglodon hydrarchus, better known as Dr Albert Koch's "Hydrarchos". Kellogg 1936, synonymized it withPontogeneus priscus, which Uhen 2005 declared a nomen dubium.
- Basilosaurus drazindai was named by Gingerich et al. 1997 based on a single lumbar vertebra. It was later declared a nomen dubium by Uhen (2013), but Gingerich and Zouhri (in press) re-assigned it to Eocetus.
- Zeuglodon elliotsmithii, Z. sensitivius, Z. sensitivus, and Z. zitteli were synonymized and grouped under the genus Saghacetus osiris by Gingerich 1992.
- Zeuglodon paulsoni from Ukraine was named by Brandt 1873. It was synonymized with Platyosphys but is now considered nomen dubium. Gingerich and Zouhri (in press), however, maintain Platyosphys as valid
- Dictionary.com, Basilosaurus
- Basilosaurus in the Paleobiology Database Retrieved May 2009
- "Basilosaurus". BBC Nature. Retrieved August 2013.
- Zalmout, Mustafa & Gingerich 2000
- "State Symbols". State of Mississippi. Retrieved August 2013.
- Gingerich, Philip D. "Basilosaurus cetoides". Encyclopedia of Alabama. Retrieved August 2013.
- "Explore Our Collections: Basilosaurus". Smithonian, National Museum of Natural History. Retrieved August 2013.
- Fahlke 2012, p. 6
- Fahlke et al. 2011
- Gingerich & Uhen 1998, p. 4
- Racicot & Berta 2013, p. 50
- Nummela et al. 2004, p. 776
- Zalmout, Mustafa & Gingerich 2000, Discussion, p. 202
- Gingerich 1998, pp. 433, 435
- Bejder & Hall 2002, p. 448
- Fahlke 2012, p. 14
- Zimmer 1998, p. 141
- Switek, Brian (September 21, 2008). "The Legacy of the Basilosaurus". ScienceBlogs. Retrieved September 2013.
- Harlan 1834, p. 400
- Harlan 1834, p. 401
- Harlan 1834, pp. 402–403
- Owen 1839, pp. 72–73
- Owen 1839, p. 75
- Gingerich 2007, pp. 110–112
- Gingerich 2007, p. 113
- Andrews 1904, pp. 214–215
- Andrews 1906, pp. 255
- Kellogg 1936, p. 81
- Gingerich 2007, p. 114
- Uhen 2004, p. 11
- Gingerich 2007, pp. 117–119
- Gingerich, Smith & Simons 1990, Abstract
- Basilosauridae in the Paleobiology Database: Taxonomic history. Retrieved August 2013.
- Kellogg 1936, p. 264
- Zeuglodon vredense (nomen nudum) in the Paleobiology Database. Retrieved August 2013.
- Kellogg 1936, p. 263
- Zeuglodon puschii (nomen dubium) in the Paleobiology Database. Retrieved August 2013.
- Basilosaurus drazindai in the Paleobiology Database. Retrieved August 2013.
- Philip D. Gingerich and Samir Zouhri (2015). "New fauna of archaeocete whales (Mammalia, Cetacea) from the Bartonian middle Eocene of southern Morocco". Journal of African Earth Sciences. in press. doi:10.1016/j.jafrearsci.2015.08.006.
- Gol'din & Zvonok 2013, Abstract
- Andrews, C. W. (1904). "Further notes on the mammals of the Eocene of Egypt. Part III.". Geological Magazine. 5 (London) 1: 211–215. doi:10.1017/s0016756800119624. Retrieved August 2013. Lay summary.
- Andrews, C. W. (1906). "A descriptive catalogue of the Tertiary Vertebrata of the Fayûm, Egypt". British Museum (Natural History) (London). OCLC 3675777. Retrieved September 2013.
- Bejder, Lars; Hall, Brian K. (2002). "Limbs in whales and limblessness in other vertebrates: mechanisms of evolutionary and developmental transformation and loss" (PDF). Evolution and Development 4 (6): 445–458. doi:10.1046/j.1525-142x.2002.02033.x.
- Brandt, J. F., von (1873). "Über bisher in Russland gefundene Reste von Zeuglodonten". Mélanges biologiques tirés du Bulletin de l'Académie impériale des sciences de St. Pétersbourg 9: 111–112. Retrieved August 2013. Lay summary (August 2013).
- Fahlke, Julia M. (2012). "Bite marks revisited – evidence for middle-to-late Eocene Basilosaurus isis predation on Dorudon atrox (both Cetacea, Basilosauridae)" (PDF). Palaeontologia Electronica 15 (3). Retrieved August 2013.
- Fahlke, Julia M.; Gingerich, Philip D.; Welsh, Robert C.; Wood, Aaron R. (2011). "Cranial asymmetry in Eocene archaeocete whales and the evolution of directional hearing in water". PNAS 108 (35): 14545–14548. doi:10.1073/pnas.1108927108. PMID 21873217.
- Gidley, J. W. (1913). "A recently mounted Zeuglodon skeleton in the United States National Museum". Proceedings of the United States National Museum (Washington) 44: 649–654. doi:10.5479/si.00963801.44-1975.649. Retrieved August 2013.
- Gingerich, P. D. (1992). "Marine Mammals (Cetacean and Sirenia) from the Eocene of Gebel Mokattam and Fayum, Egypt: Stratigraphy, Age, and Paleoenvironments". University of Michigan Papers on Paleontology 30: 1–84. OCLC 26941847. Retrieved May 2013.
- Gingerich, P. D. (1998). "Paleobiological Perspectives on Mesonychia, Archaeoceti, and the Origin of Whales". In Thewissen, J. G. M. The Emergence of Whales: Evolutionary Patterns in the Origin of Cetacea (PDF). Advances in Vertebrate Paleobiology 1. Springer. pp. 424–439. ISBN 9780306458538. Retrieved September 2013.
- Gingerich, P. D. (2007). "Early evolution of whales: a century of research in Egypt". In Fleagle, J. G.; Gilbert, Christopher C. Elwyn Simons: A Search for Origins (PDF). New York: Springer. pp. 107–124. ISBN 978-0-387-73896-3. OCLC 233971398. Retrieved August 2013.
- Gingerich, P. D.; Arif, M; Bhatti, M Akram; Anwar, M; Sanders, William J (1997). "Basilosaurus drazindai and Basiloterus hussaini, New Archaeoceti (Mammalia, Cetacea) from the Middle Eocene Drazinda Formation, with a Revised Interpretation of Ages of Whale-Bearing Strata in the Kirthar Group of the Sulaiman Range, Punjab (Pakistan)". Contributions from the Museum of Paleontology, University of Michigan 30 (2): 55–81. OCLC 742731913.
- Gingerich, Philip D.; Smith, B. Holly; Simons, Elwyn L. (1990). "Hind Limbs of Eocene Basilosaurus: Evidence of Feet in Whales". Science 249 (4965): 154–157. doi:10.1126/science.249.4965.154.
- Gingerich, P. D.; Uhen, Mark D. (1998). "Likelihood estimation of the time of origin of Cetacea and the time of divergence of Cetacea and Artiodactyla" (PDF). Palaeontologia Electronica 1 (2): 1–45. Retrieved September 2013.
- Gol'din, Pavel; Zvonok, Evgenij (2013). "Basilotritus uheni, a New Cetacean (Cetacea, Basilosauridae) from the Late Middle Eocene of Eastern Europe". Journal of Paleontology 87 (2): 254–268. doi:10.1666/12-080R.1.
- Harlan, R. (1834). "Notice of fossil bones found in the Tertiary formation of the State of Louisiana". Transactions of the American Philosophical society 4: 397–403. JSTOR 1004838. OCLC 63356837. Retrieved August 2013.
- Kellogg, R. (1923). "Description of two squalodonts recently discovered in the Calvert Cliffs, Maryland; and notes on the shark-toothed cetaceans". Proceedings of the United States National Museum 62 (2462): 1–69. doi:10.5479/si.00963801.62-2462.1. OCLC 82628874. Retrieved August 2013.
- Kellogg, R. (1936). A review of the Archaeoceti (PDF, 46 Mb). Washington: Carnegie Institution of Washington. OCLC 681376. Retrieved July 2013.
- Lucas, Frederic A. (1900). "The pelvic girdle of Zeuglodon, Basilosaurus cetoides (Owen) with notes on other portions of the skeleton" (PDF). Proceedings of the United States National Museum 23 (1211): 327–331. doi:10.5479/si.00963801.23-1211.327. OCLC 75278090. Retrieved September 2013.
- Lydekker, R. (1892). "4. On Zeuglodont and other Cetacean Remains from the Tertiary of the Caucasus". Proceedings of the Zoological Society of London 60 (4): 558–581. doi:10.1111/j.1096-3642.1892.tb01782.x. OCLC 819196877. Lay summary.
- Müller, Johannes Peter (1849). Über die fossilen Reste der Zeuglodonten von Nordamerika mit Rücksicht auf die europäischen Reste aus dieser Familie. Berlin: Reiner. pp. 1–38. OCLC 422134028. Lay summary.
- Nummela, Sirpa; Thewissen, J. G. M.; Bajpai, Sunil; Hussain, Taseer; Kumar, Kishor (2004). "Eocene evolution of whale hearing" (PDF). Nature 430: 776–778. doi:10.1038/nature02720. PMID 15306808. Retrieved September 2013.
- Owen, R. (1839). "Observations on the Basilosaurus of Dr. Harlan (Zeuglodon cetoides, Owen)". Transaction of the Geological Society of London 6: 69–79. doi:10.1144/transgslb.6.1.69. Retrieved August 2013. Lay summary.
- Racicot, Rachel A.; Berta, Annalisa (2013). "Comparative Morphology of Porpoise (Cetacea: Phocoenidae) Pterygoid Sinuses: Phylogenetic and Functional Implications". Journal of Morphology 274 (1): 49–62. doi:10.1002/jmor.20075. Retrieved September 2013.
- Sanger, E. B. (1881). "On a molar tooth of Zeuglodon from the Tertiary beds on the Murray River near Wellington, S.A.". Proceedings of the Linnean Society of New South Wales 1 (5): 298–300. Retrieved August 2013. Lay summary.
- Tinker, Spencer Wilkie (1988). Whales of the World. Brill Archive. ISBN 9780935848472.
- Uhen, Mark D. (2002). "Basilosaurids". In Perrin, William F.; Würsig, Bernd; Thewissen, J. G. M. Encyclopedia of Marine Mammals. Academic Press. pp. 79–81. ISBN 0-12-551340-2.
- Uhen, Mark D. (2004). "Form, Function, and Anatomy of Dorudon Atrox (Mammalia, Cetacea): An Archaeocete from the Middle to Late Eocene of Egypt". Papers on Paleontology (University of Michigan) 34. Retrieved July 2013.
- Uhen, M. D. (2005). "A new genus and species of archaeocete whale from Mississippi". Mississippi Geology 43 (3): 157–172.
- Zalmout, I. S.; Mustafa, H. A.; Gingerich, P. D. (2000). "Priabonian Basilosaurus isis (Cetacea) from the Wadi Esh-Shallala Formation: first marine mammal from the Eocene of Jordan" (PDF). Journal of Vertebrate Paleontology 20 (1): 201–204. doi:10.1671/0272-4634(2000)020[0201:pbicft]2.0.co;2. OCLC 4908948040. Retrieved August 2013.
- Zimmer, Carl (1998). At the Water's Edge: Macroevolution and the Transformation of Life. Free Press. ISBN 9780684834900.
|Wikimedia Commons has media related to Basilosaurus.|
- "Cetartiodactyla: Cetacea: Basilosauridae". Palaeos Vertebrates. March 2012. Retrieved September 2013.