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This article is about the snake genus. For the documentary, see Titanoboa: Monster Snake.

Titanoboa
Temporal range: Mid-Late Paleocene (Peligran-Itaboraian)
~60–58 Ma
↓
Titanoboa dorsal vertebra in the José Royo y Gómez National Geological Museum, Bogotá
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Serpentes
Family: Boidae
Genus: †Titanoboa
Head et al., 2009
Species:
†T. cerrejonensis
Binomial name
†Titanoboa cerrejonensis
Head et al., 2009

Titanoboa (/ˌtaɪtənəˈboʊə/; lit. 'titanic boa') is an extinct genus of giant boid (the family that includes all boas and anacondas) snake that lived during the middle and late Paleocene. Titanoboa was first discovered in the early 2000s by the Smithsonian Tropical Research Institute who, along with students from the University of Florida, recovered 186 fossils of Titanoboa from La Guajira in northeastern Colombia. It was named and described in 2009 as Titanoboa cerrejonensis, the largest snake ever found at that time. It was originally known only from thoracic vertebrae and ribs, but later expeditions collected parts of the skull and teeth. Titanoboa is in the subfamily Boinae, being most closely related to other extant boines from Madagascar and the Pacific.

Titanoboa could grow up to 12.8 m (42 ft) long, perhaps even up to 14.3 m (47 ft) long, and weigh around 730–1,135 kg (1,610–2,500 lb). The discovery of Titanoboa cerrejonensis supplanted the previous record holder, Gigantophis garstini, which is known from the Eocene of Egypt. Titanoboa evolved following the extinction of all non-avian dinosaurs, being one of the largest reptiles to evolve after the Cretaceous–Paleogene extinction event. Its vertebrae are very robust and wide, with a pentagonal shape in anterior view, as in other members of Boinae. Although originally thought to be an apex predator, the discovery of skull bones revealed that it was more than likely specialized in preying on fish.

History and naming

Main articles: Cerrejón Formation and Cerrejón

In 2002, during an expedition to the coal mines of Cerrejón in La Guajira[1] launched by the University of Florida and Smithsonian Tropical Research Institute,[2] large thoracic vertebrae and ribs were unearthed by the students Jonathon Bloch and Carlos Jaramillo.[3][4] More fossils were unearthed over the course of the expedition, eventually totaling 186 fossils from 30 individuals.[2] The expedition lasted until 2004, during which the fossils of Titanoboa were mistakenly labeled as those of crocodiles.[5] These were found in association with other giant reptile fossils of turtles and crocodilians from the Cerrejón Formation, dating to the mid-late Paleocene epoch (around 60-58 mya), a period just after the Cretaceous–Paleogene extinction event.[2] Before this discovery, few fossils of Paleocene-epoch vertebrates had been found in ancient tropical environments of South America.[6] The fossils were then transported to the Florida Museum of Natural History, where they were studied and described by an international team of Canadian, American, and Panamanian scientists in 2009 led by Jason J. Head of the University of Toronto.[2] The snake elements were described as those of a novel, giant boid snake that they named Titanoboa cerrejonensis. The genus name derives from the Greek word "Titan" in addition to Boa, the type genus of the family Boidae. The species name is a reference to the Cerrejón region it is known from.[2]

Another expedition to Cerrejón launched in 2011 found more fossils from Titanoboa.[5] Most notably, the group returned with three disarticulated skulls of Titanoboa, making it one of the few fossil snakes with preserved cranial material. They were associated with postcranial material, cementing their referral to the species.[7] Though the skulls are undescribed, an article by the BBC in 2012[8] and an abstract in the Society of Vertebrate Paleontology have been published.[7] A documentary on the animal titled Titanoboa: Monster Snake aired in 2012 in addition to a touring exhibit of the same name, which lasted from 2013 to 2018.[9]

Description

Size

The relative size of Titanoboa to the modern human, Palaeophis, Gigantophis, reticulated python, and green anaconda.

Based on the size of the vertebrae, Titanoboa is the largest snake in the paleontological record. In modern constrictors like boids and pythonids, increased body size is achieved through larger vertebrae rather than an increase in the number of bones making up the skeleton, allowing for length estimates based on individual bones. Based on comparison between the undistorted Titanoboa vertebrae and the skeleton of modern boas, Head and colleagues found that the analyzed specimens fit a position towards the later half of the precloacal vertebral column, approximately 60 to 65% back from the first two neck vertebrae. Using this method, initial size estimates proposed a total body length of approximately 12.82 m (42.1 ft) (± 2.18 m (7 ft 2 in)). Weight was determined by comparing Titanoboa to the extant green anaconda and the southern rock python, resulting in a weight between 652 kg (1,437 lb) and 1,819 kg (4,010 lb) (mean estimate 1,135 kg (2,502 lb)). These estimates far exceed the largest modern snakes, the green anaconda and the reticulated python, as well as the previous record holder, the madtsoid Gigantophis. The existence of eight additional specimens of similar size to the one used in these calculations implies that Titanoboa reached such massive proportions regularly.[2] The later discovery of skull material allowed for size estimates based on skull to body length proportions. Applying anaconda proportions to the 40 cm (16 in) skull of Titanoboa results in a total body length of around 14.3 m (47 ft) (± 1.28 m (4 ft 2 in)).[7] In 2016, Feldman and his colleagues estimated that a 12.8 m (42 ft) long individual would have weighed 730 kg (1,610 lb) at maximum based on their equation to estimate the body size of boids.[10]

Anatomy

Life restoration

Many of the fossils of Titanoboa are incomplete or undescribed, consisting primarily of thoracic vertebrae that were located before the cloaca. It possesses the same characteristics as other boids and especially Boa, such as a short, posteriorly-pointing prezygapophyseal process on these vertebrae. However, Titanoboa's are distinct due to being very robust and with a uniquely T-shaped neural spine. The neural spine also has an expanded posterior margin and a thin, blade-like anterior process. It also has much smaller foramina (small pits in bone) on its center and lateral sides, contrary to those of many other boids.[2]

The skull is only briefly described in a 2013 abstract. According to it, Titanoboa has a high amount of palatal and marginal tooth positions compared to others boids. The quadrate bone is oriented at a low angle and the articulation of both the palatine to pterygoid and pterygoid to quadrate are heavily reduced, a trait absent in its relatives. The teeth themselves are weakly ankylosed, meaning they are not strongly connected to the jawbone.[7]

Classification

Titanoboa is placed in the family Boidae, a family of snakes containing the "constrictors", that evolved during the Late Cretaceous in what is now the Americas.[11] They are a widely distributed group, with six subfamilies found on nearly every continent,[12] with Titanoboa being in the subfamily Boinae based on vertebrae morphology. All known boines are from the Americas, reaching as far north as Mexico and the Antilles[13] and south to Argentina.[14] Titanoboa is also the only extinct boine genus known; all other boine genera are still living.[15][2]

The skull material confirmed Titanoboa's initial placement within the subfamily, now also supported by the reduced palatine choanal. The 2013 abstract recovered Titanoboa as closely related to taxa from the Pacific Islands and Madagascar, linking the Old World and New World boids and suggesting that the two lineages diverged by the Paleocene at the latest.[7] This would place Titanoboa at the stem of Boinae, a result corroborated by a study in 2015.[11]

The cladogram below follows the 2015 phylogenetic analysis:[11]

Palaeobiology

Habitat

Example of a coal mine in Cerrejón, where Titanoboa was found.

Due to the warm and humid greenhouse climate of the Paleocene, the region of what is now Cerrejón was a coastal plain covered by wet tropical forests with large river systems, which were inhabited by various freshwater animals. Among the native reptiles are three different genera of dyrosaurs, crocodylomorphs that survived the KPG extinction event independently from modern crocodilians. The genera that coexisted alongside Titanoboa included the large, slender-snouted Acherontisuchus, the medium-sized but broad-headed Anthracosuchus, and the relatively small Cerrejonisuchus.[16][17] Turtles also thrived in the tropical wetlands of Paleocene Colombia, giving rise to several species of considerable size such as Cerrejonemys[18] and Carbonemys.[19]

The rainforests of the Cerrejón Formation mirror modern tropical forests in regards to which families make up most of the vegetation. But unlike modern tropical forests, these Paleocene forests had fewer species. Although it is possible that this low diversity was a result of the wetland nature of the depositional environment, samples from other localities in the same time frame suggest that all of the forests that arose shortly following the Cretaceous-Paleogene mass extinction were of similar composition. This indicates that the low plant diversity of the time was a direct result of the mass extinction preceding it.[20][21] Plants found in these Paleocene forests include the floating fern Salvinia[22] and various genera of Zingiberales and Araceae.[23]

Diet

Initially, Titanoboa was thought to have acted much like a modern anaconda based on its size and the environment it lived in, with researchers suggesting that it may have fed on the local crocodylomorph fauna. However, in the 2013 abstract, Jason Head and colleagues noted that the skull of this snake displays multiple adaptations to a piscivorous diet, including the anatomy of the palate, the tooth count, and the anatomy of the teeth themselves. These adaptations are not seen in other boids, but closely resemble those in modern caeonphidian snakes with a piscivorous diet. Such a lifestyle would be supported by the extensive rivers of Paleocene Colombia, as well as the fossil fish (lungfish and osteoglossomorphs) recovered from the formation.[7]

Climate implications

In the 2009 type description, Head and colleagues correlate the gigantism observed in Titanoboa with the climate conditions of its environment. As a poikilothermic ectotherm, Titanoboa's internal temperature and metabolism were heavily dependent on the ambient temperature, which would in turn affect the animal's size.[24] Accordingly, large ectothermic animals are typically found in the tropics and decrease in size the further one moves away from the equator. Following this correlation, the authors suggest that the mean annual temperature can be calculated by comparing the maximum body size of poikilotherm animals found in two localities. Based on the relation between temperatures in the modern Neotropics and the maximum length of anacondas, Head and colleagues calculated a mean annual temperature of at least 32–33 °C (90–91 °F) for the equatorial region of Paleocene South America. The estimates are consistent with a hot Paleocene climate as suggested by a study published in 2003[25] and slightly higher (1–5 °C) than estimates derived from the oxygen isotopes of planktonic foraminifer. Although these estimates exceed temperatures of modern tropical forests, the paper argued that the increase in temperature was balanced out by higher amounts of rainfall.[2]

However, this conclusion was questioned by several researchers following the publication of the paper. J. M. Kale Sniderman used the same methodology as Head and colleagues on the Pleistocene monitor lizard Varanus priscus, comparing it to the extant Komodo dragon. Sniderman calculates that following this method, the modern tropics should be able to support lizards much larger than what is observed today, or in the reverse, that Varanus priscus is much larger than what would be implied by the ambient temperature of its native range. In conclusion it is argued that Paleocene rainforests may not have been any hotter than those today and that the massive size of Titanoboa and Varanus priscus may instead be the result of lacking significant mammalian competition.[26] Mark W. Denny, Brent L. Lockwood and George N. Somero also disagreed with Head's conclusion, noting that although this method is applicable to smaller poikilotherms, it is not constant across all size ranges. As thermal equilibrium is achieved through the relation between volume and surface area, they argue that the large size of Titanoboa coupled with the high temperatures proposed by Head et al. would mean that the animal would overheat easily if resting in a coiled up state. The authors conclude that several key factors influence the relationship between Titanoboa and the temperature of the area it inhabited. Varying posture could help cool down if needed, basking behavior or heat absorption through the substrate are both unknown and the potentially semi-aquatic nature of the animal creates additional factors to consider. Ultimately, Denny and colleagues argue that the nature of the giant snake renders it a poor indicator for the climate of the Paleocene and that the mean annual temperature must have been 4 to 6 °C (7 to 11 °F) cooler than the current estimate.[27]

These issues, alongside adjustments suggested by Makarieva, were addressed by Head and his team the same year, arguing that Denny and colleagues misunderstand their proposed model. They retort that the method takes into account variation caused by body size and that it's furthermore based on the largest extant snakes, making it an appropriate method. They also add that the results recovered are consistent with large extant snakes, which are also known to perform thermoregulation through behavior. Sniderman's proposal that the correlation between body size and temperature is inconsistent with modern monitor lizards is addressed twofold. For one, Head argues, Komodo dragons are a poor analogy as they are geographically restricted to the islands of Indonesia, limiting the size they could grow to while both green anacondas and Titanoboa are mainland animals. Secondly the response notes that the size estimates utilized for Varanus priscus are overestimates and unreliable, being based on secondary reports that do not match better supported estimates indicating a 2.19–4.7 m (7 ft 2 in – 15 ft 5 in) range for the monitor.[28]

See also

References

  1. ^ Template:Cite LSA
  2. ^ a b c d e f g h i Head, J.J.; Bloch, J.I.; Hastings, A.K.; Bourque, J.R.; Cadena, E.A.; Herrera, F.A.; Polly, P.D.; Jaramillo, C.A. (2009). "Giant boid snake from the Paleocene neotropics reveals hotter past equatorial temperatures". Nature. 457 (7230): 715–717. Bibcode:2009Natur.457..715H. doi:10.1038/nature07671. PMID 19194448. S2CID 4381423.
  3. ^ Kwok, R. (4 February 2009). "Scientists find world's biggest snake". Nature News. doi:10.1038/news.2009.80.
  4. ^ "At 2,500 Pounds And 43 Feet, Prehistoric Snake Is Largest On Record". Science Daily. 4 February 2009. Retrieved 6 February 2009.
  5. ^ a b "How Titanoboa, the 40-Foot-Long Snake, Was Found". Smithsonian Magazine. Retrieved 7 June 2023.
  6. ^ Maugh II, T.H. (4 February 2009). "Fossil of 43-foot super snake Titanoboa found in Colombia". Los Angeles Times. Retrieved 4 February 2009.
  7. ^ a b c d e f Template:Cite LSA
  8. ^ O'Brien, Jane (2 April 2012). "The giant snake that stalked the Earth". BBC News. Retrieved 22 May 2017.
  9. ^ "Titanoboa: Monster Snake". Smithsonian. 2012. Retrieved 10 June 2023.
  10. ^ Feldman, A.; Sabath, N.; Pyron, R.A.; Mayrose, I.; Meiri, S. (2016). "Body sizes and diversification rates of lizards, snakes, amphisbaenians and the tuatara". Global Ecology and Biogeography. 25 (2): 187–197. doi:10.1111/geb.12398. S2CID 25049185.
  11. ^ a b c Head, JJ (2015). "Fossil calibration dates for molecular phylogenetic analysis of snakes 1: Serpentes, Alethinophidia, Boidae, Pythonidae". Palaeontologia Electronica. doi:10.26879/487. ISSN 1094-8074.
  12. ^ McDiarmid, R.W.; Campbell, J.A.; Touré. T. 1999. Snake Species of the World: A Taxonomic and Geographic Reference Vol. 1. Herpetologists' League. 511 pp. ISBN 1-893777-00-6 (series). ISBN 1-893777-01-4 (volume).
  13. ^ IUCN (20 August 2018). "Boa imperator: Montgomery, C.E. & da Cunha, O." The IUCN Red List of Threatened Species 2018: e.T203879A2771951. doi:10.2305/iucn.uk.2018-2.rlts.t203879a2771951.en. S2CID 240344156.
  14. ^ "ITIS - Report: Epicrates cenchria". www.itis.gov. Retrieved 9 June 2023.
  15. ^ Lotte, Jose; Lotte, Ben (1996). "Taxonomy and Description of Boa Constrictor". Litteratura Serpentium. 16 (3): 78–81.
  16. ^ Hastings, Alexander K.; Bloch, Jonathan I.; Jaramillo, Carlos A. (17 November 2015). "A new blunt-snouted dyrosaurid, Anthracosuchus balrogus gen. et sp. nov. (Crocodylomorpha, Mesoeucrocodylia), from the Palaeocene of Colombia". Historical Biology. 27 (8): 998–1020. doi:10.1080/08912963.2014.918968. ISSN 0891-2963.
  17. ^ Hastings, Alexander K.; Bloch, Jonathan I.; Jaramillo, Carlos A. (2011). "A new longirostrine dyrosaurid (Crocodylomorpha, Mesoeucrocodylia) from the Paleocene of north-eastern Colombia: biogeographic and behavioural implications for New-World Dyrosauridae: SECOND NEW DYROSAURID FROM COLOMBIA". Palaeontology. 54 (5): 1095–1116. doi:10.1111/j.1475-4983.2011.01092.x. S2CID 84094253.
  18. ^ Template:Cite LSA
  19. ^ Template:Cite LSA
  20. ^ Template:Cite LSA
  21. ^ Template:Cite LSA
  22. ^ Pérez Consuegra, Nicolás; Cuervo Gómez, Aura; Martínez, Camila; Montes, Camilo; Herrera, Fabiany; Madriñán, Santiago; Jaramillo, Carlos (2017). "Paleogene Salvinia (Salviniaceae) from Colombia and their paleobiogeographic implications". Review of Palaeobotany and Palynology. 246: 85–108. Bibcode:2017RPaPa.246...85P. doi:10.1016/j.revpalbo.2017.06.003.
  23. ^ Herrera, Fabiany A.; Jaramillo, Carlos A.; Dilcher, David L.; Wing, Scott L.; Gómez N., Carolina (2008). "Fossil Araceae from a Paleocene neotropical rainforest in Colombia". American Journal of Botany. 95 (12): 1569–1583. doi:10.3732/ajb.0800172. PMID 21628164.
  24. ^ Makarieva, Anastassia M.; Gorshkov, Victor G.; Li, Bai-Lian (2005). "Gigantism, temperature and metabolic rate in terrestrial poikilotherms". Proceedings of the Royal Society B. 272 (1578): 2325–2328. doi:10.1098/rspb.2005.3223. PMC 1560189. PMID 16191647.
  25. ^ Shellito, C.J.; Sloan, L.C.; Huber, M. (2003). "Climate model sensitivity to atmospheric CO2 levels in the Early–Middle Paleogene". Palaeogeography, Palaeoclimatology, Palaeoecology. 193 (1): 113–123. Bibcode:2003PPP...193..113S. doi:10.1016/S0031-0182(02)00718-6.
  26. ^ Sniderman, J.M.K (2009). "Biased reptilian palaeothermometer?". Nature. 460 (7255): E1–E2. Bibcode:2009Natur.460....1S. doi:10.1038/nature08222. S2CID 4322274.
  27. ^ Denny, Mark W.; Lockwood, Brent L.; Somero, George (2009). "Can the giant snake predict palaeoclimate?". Nature. 460 (7255): E3–E4. Bibcode:2009Natur.460....3D. doi:10.1038/nature08224. S2CID 41962223.
  28. ^ Head, J.J.; Bloch, J.I.; Hastings, A.K.; Bourque, J.R.; Cadena, E.A.; Herrera, F.A.; Polly, P.D.; Jaramillo, C.A. (2009). "Head et al. reply". Nature. 460 (7255): E4–E5. Bibcode:2009Natur.460....4H. doi:10.1038/nature08225. S2CID 4420868.
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