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Temporal range: Late Cretaceous, Upper Maastrichtian, 68–66 Ma
Restored Quetzalcoatlus skeleton
displayed in quadrupedal stance,
Houston Museum of Natural Science
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Order: Pterosauria
Suborder: Pterodactyloidea
Family: Azhdarchidae
Genus: Quetzalcoatlus
Lawson, 1975
Type species
Quetzalcoatlus northropi
Lawson, 1975

Quetzalcoatlus northropi /kɛtsəlkˈætləs, kwɛ-/ is a pterosaur known from the Late Cretaceous of North America (Maastrichtian stage) and one of the biggest known flying animals of all time. It is a member of the family Azhdarchidae, a family of advanced toothless pterosaurs with unusually long, stiffened necks. Its name comes from the Aztec feathered serpent god, Quetzalcoatl.

Discovery and species

Cast of the holotype humerus

The first Quetzalcoatlus fossils were discovered in Texas, United States, from the Maastrichtian Javelina Formation at Big Bend National Park (dated to around 68 million years ago[1]) in 1971 by Douglas A. Lawson, a geology graduate student from the Jackson School of Geosciences at the University of Texas at Austin. The specimen consisted of a partial wing (in pterosaurs composed of the forearms and elongated fourth finger), from an individual later estimated at over 10 m (33 ft) in wingspan.[2]

Lawson discovered a second site of the same age, about 40 km (25 mi) from the first, where between 1972 and 1974 he and Professor Wann Langston Jr. of the Texas Memorial Museum unearthed three fragmentary skeletons of much smaller individuals. Lawson in 1975 announced the find in an article in Science.[3] That same year, in a subsequent letter to the same journal, he made the original large specimen, TMM 41450-3, the holotype of a new genus and species, Quetzalcoatlus northropi. The genus name refers to the Aztec feathered serpent god, Quetzalcoatl. The specific name honors John Knudsen Northrop, the founder of Northrop, who drove the development of large tailless flying wing aircraft designs resembling Quetzalcoatlus.[4]

Skeletal reconstruction of Q. sp.

At first it was assumed that the smaller specimens were juvenile or subadult forms of the larger type. Later, when more remains were found, it was realized they could have been a separate species. This possible second species from Texas was provisionally referred to as a Quetzalcoatlus sp. by Alexander Kellner and Langston in 1996, indicating that its status was too uncertain to give it a full new species name.[5] The smaller specimens are more complete than the Q. northropi holotype, and include four partial skulls, though they are much less massive, with an estimated wingspan of 5.5 m (18 ft).[6]

The holotype specimen of Q. northropi has yet to be properly described and diagnosed, and the current status of the genus Quetzalcoatlus has been identified as problematic. Mark Witton and colleagues (2010) noted that the type species of the genus—the fragmentary wing bones comprising Q. northropi—represent elements which are typically considered undiagnostic to generic or specific level, and that this complicates interpretations of azhdarchid taxonomy. For instance, Witton et al. (2010) suggested that the Q. northropi type material is of generalised enough morphology to be near identical to that of other giant azhdarchids, such as the overlapping elements of the contemporary Romanian giant azhdarchid Hatzegopteryx. This being the case, and assuming Q. northropi can be distinguished from other pterosaurs (i.e., if it is not a nomen dubium), perhaps Hatzegopteryx should be regarded as a European occurrence of Quetzalcoatlus. However, Witton et al. also noted that the skull material of Hatzegopteryx and Q. sp. differ enough that they cannot be regarded as the same animal, but that the significance of this cannot be ascertained given uncertainty over the relationships of Quetzalcoatlus specimens.[7] These issues can only be resolved by Q. northropi being demonstrated as a valid taxon and its relationships with Q. sp. being investigated. An additional complication to these discussions are the likelihood that huge pterosaurs such as Q. northropi could have made long, transcontinental flights, suggesting that locations as disparate as North America and Europe could have shared giant azhdarchid species.[7]

An azhdarchid neck vertebra, discovered in 2002 from the Maastrichtian age Hell Creek Formation, may also belong to Quetzalcoatlus. The specimen (BMR P2002.2) was recovered accidentally when it was included in a field jacket prepared to transport part of a Tyrannosaurus specimen. Despite this association with the remains of a large carnivorous dinosaur, the vertebra shows no evidence that it was chewed on by the dinosaur. The bone came from an individual azhdarchid pterosaur estimated to have had a wingspan of 5–5.5 m (16–18 ft).[8]



Size comparison of a human to Q. northropi (green) and Q. sp. (blue)
Comparison of Q. northropi with a Cessna 172 light aircraft

When it was first named as a new species in 1975, scientists estimated that the largest Quetzalcoatlus fossils came from an individual with a wingspan as large as 15.9 m (52 ft). Choosing the middle of three extrapolations from the proportions of other pterosaurs gave an estimate of 11 m, 15.5 m, and 21 m, respectively (36 ft, 50.85 ft, 68.9 ft). In 1981, further advanced studies lowered these estimates to 11–12 m (36–39 ft).[9]

More recent estimates based on greater knowledge of azhdarchid proportions place its wingspan at 10–11 m (33–36 ft).[7] Remains found in Texas in 1971 indicate that this reptile had a minimum wingspan of about 11 m (36 ft).[10] Generalized height in a bipedal stance, based on its wingspan, would have been at least 3 m (9.8 ft) high at the shoulder.[2]

Weight estimates for giant azhdarchids are extremely problematic because no existing species share a similar size or body plan, and in consequence, published results vary widely.[2] Generalized weight, based on some studies that have historically found extremely low weight estimates for Quetzalcoatlus, was as low as 70 kg (150 lb) for a 10 m (32 ft 10 in) individual. A majority of estimates published since the 2000s have been substantially higher, around 200–250 kg (440–550 lb).[11][12]

Skull reconstruction of Q. sp.


Skull material (from smaller specimens, possibly a related species) shows that Quetzalcoatlus had a very sharp and pointed beak. That is contrary to some earlier reconstructions that showed a blunter snout, based on the inadvertent inclusion of jaw material from another pterosaur species, possibly a tapejarid or a form related to Tupuxuara. A skull crest was also present but its exact form and size are still unknown.[5]


A comparison of Quetzalcoatlus cervical vertebrae on the left with the Phosphatodraco holotype on the right

Below is a cladogram showing the phylogenetic placement of Quetzalcoatlus within Neoazhdarchia from Andres and Myers (2013).[13]


Thalassodromeus sethi

Tupuxuara leonardii

Tupuxuara longicristatus


Domeykodactylus ceciliae

Dsungaripterus weii

Noripterus complicidens

Noripterus parvus


Eoazhdarcho liaoxiensis

Shenzhoupterus chaoyangensis

Chaoyangopterus zhangi

Jidapterus edentus

Radiodactylus langstoni


Azhdarcho lancicollis

TMM 42489

Zhejiangopterus linhaiensis

Arambourgiania philadelphiae

Quetzalcoatlus northropi

Quetzalcoatlus sp.


Quetzalcoatlus was abundant in Texas during the Lancian in a fauna dominated by Alamosaurus.[14] The Alamosaurus-Quetzalcoatlus association probably represents semi-arid inland plains.[14] Quetzalcoatlus had precursors in North America and its apparent rise to widespreadness may represent the expansion of its preferred habitat rather than an immigration event, as some experts have suggested.[14]


Artist's impression of a group of Quetzalcoatlus feeding on the ground

There have been a number of different ideas proposed about the lifestyle of Quetzalcoatlus. Because the area of the fossil site was four hundred kilometers removed from the coastline and there were no indications of large rivers or deep lakes nearby at the end of the Cretaceous, Lawson in 1975 rejected a fish-eating lifestyle, instead suggesting that Quetzalcoatlus scavenged like the marabou stork (which will scavenge, but is more of a terrestrial predator of small animals), but then on the carcasses of titanosaur sauropods such as Alamosaurus. Lawson had found the remains of the giant pterosaur while searching for the bones of this dinosaur, which formed an important part of its ecosystem.[3]

In 1996, Lehman and Langston rejected the scavenging hypothesis, pointing out that the lower jaw bent so strongly downwards that even when it closed completely a gap of over five centimeters remained between it and the upper jaw, very different from the hooked beaks of specialized scavenging birds. They suggested that with its long neck vertebrae and long toothless jaws Quetzalcoatlus fed like modern-day skimmers, catching fish during flight while cleaving the waves with its beak.[15] While this skim-feeding view became widely accepted, it was not subjected to scientific research until 2007 when a study showed that for such large pterosaurs it was not a viable method because the energy costs would be too high due to excessive drag.[16] In 2008 pterosaur workers Mark Witton and Darren Naish published an examination of possible feeding habits and ecology of azhdarchids. Witton and Naish noted that most azhdarchid remains are found in inland deposits far from seas or other large bodies of water required for skimming. Additionally, the beak, jaw, and neck anatomy are unlike those of any known skimming animal. Rather, they concluded that azhdarchids were more likely terrestrial stalkers, similar to modern storks, and probably hunted small vertebrates on land or in small streams. Though Quetzalcoatlus, like other pterosaurs, was a quadruped when on the ground, Quetzalcoatlus and other azhdarchids have fore and hind limb proportions more similar to modern running ungulate mammals than to their smaller cousins, implying that they were uniquely suited to a terrestrial lifestyle.[2]


Artist's impression of an individual in flight

The nature of flight in Quetzalcoatlus and other giant azhdarchids was poorly understood until serious biomechanical studies were conducted in the 21st century. One early (1984) experiment by Paul MacCready used practical aerodynamics to test the flight of Quetzalcoatlus. MacCready constructed a model flying machine or ornithopter with a simple computer functioning as an autopilot. The model successfully flew with a combination of soaring and wing flapping;[17] the model was based on a then-current weight estimate of around 80 kg (180 lb), far lower than more modern estimates of over 200 kg (440 lb).[18] The method of flight in these pterosaurs depends largely on weight, which has been controversial, and widely differing masses have been favored by different scientists. Some researchers have suggested that these animals employed slow, soaring flight, while others have concluded that their flight was fast and dynamic.[2] In 2010, Donald Henderson argued that the mass of Q. northropi had been underestimated, even the highest estimates, and that it was too massive to have achieved powered flight. He estimated it in his 2010 paper as 540 kg (1,190 lb). Henderson argued that it may have been flightless.[18]

Reconstructed skeleton at the Royal Ontario Museum

Other flight capability estimates have disagreed with Henderson's research, suggesting instead an animal superbly adapted to long-range, extended flight. In 2010, Mike Habib, a professor of biomechanics at Chatham University, and Mark Witton, a British paleontologist, undertook further investigation into the claims of flightlessness in large pterosaurs. After factoring wingspan, body weight, and aerodynamics, computer modelling led the two researchers to conclude that Q. northropi was capable of flight up to 130 km/h (80 mph) for 7 to 10 days at altitudes of 4,600 m (15,000 ft). Habib further suggested a maximum flight range of 13,000–19,000 km (8,000–12,000 mi) for Q. northropi.[19] Henderson's work was also further criticized by Witton and Habib in another study, which pointed out that although Henderson used excellent mass estimations, they were based on outdated pterosaur models, which caused Henderson's mass estimations to be more than double what Habib used in his estimations, and that anatomical study of Q. northropi and other big pterosaur forelimbs showed a higher degree of robustness than would be expected if they were purely quadrupedal.[12] This study proposed that large pterosaurs most likely utilized a short burst of powered flight to then transition to thermal soaring.[20]

Cultural significance

In 1975, artist Giovanni Casselli depicted Quetzalcoatlus as a small-headed scavenger with an extremely long neck in the book The evolution and ecology of the Dinosaurs[21] by British palaeontologist Beverly Halstead. Over the next twenty-five years prior to future discoveries, it would launch similar depictions colloquially known as a Paleomeme in various books as noted by Darren Naish.[22]

Models on London's South Bank for the Royal Society's 350th anniversary exhibition

In June 2010, several life-sized models of Q. northropi were put on display on London's South Bank as the centerpiece exhibit for the Royal Society's 350th-anniversary exhibition. The models, which included both flying and standing individuals with wingspans of 9 m (30 ft), were intended to help build public interest in science. The models were created by scientists from the University of Portsmouth and engineers from Griffon Hoverwork. The display featured the most accurate pterosaur models constructed at the time; these models took into account the latest evidence based on skeletal and trace fossils from related pterosaurs.[23]

In 1985, the US Defense Advanced Research Projects Agency (DARPA) and AeroVironment used Quetzalcoatlus northropi as the basis for an experimental ornithopter unmanned aerial vehicle (UAV). They produced a half-scale model weighing 18 kg (40 lb), with a wingspan of 5.5 m (18 ft). Coincidentally, Douglas A. Lawson, who discovered Q. northropi in Texas in 1971, named it after John "Jack" Northrop, a developer of tailless flying wing aircraft in the 1940s.[24] The replica of Q. northropi incorporates a "flight control system/autopilot which processes pilot commands and sensor inputs, implements several feedback loops, and delivers command signals to its various servo-actuators". It is on exhibit at the National Air and Space Museum.[25]

See also


  1. Lehman, Thomas M.; Mcdowell, Fred W.; Connelly, James N. (11 December 2006). "First isotopic (U-Pb) age for the Late Cretaceous Alamosaurus vertebrate fauna of West Texas, and its significance as a link between two faunal provinces". Journal of Vertebrate Paleontology. 26 (4): 922–928. doi:10.1671/0272-4634(2006)26[922:FIUAFT]2.0.CO;2.
  2. 1 2 3 4 5 Witton, Mark P.; Naish, Darren (28 May 2008). "A Reappraisal of Azhdarchid Pterosaur Functional Morphology and Paleoecology". PLOS ONE. 3 (5): e2271. Bibcode:2008PLoSO...3.2271W. doi:10.1371/journal.pone.0002271. PMC 2386974. PMID 18509539.
  3. 1 2 Lawson, Douglas A. (14 March 1975). "Pterosaur from the Latest Cretaceous of West Texas: Discovery of the Largest Flying Creature". Reports. Science. 187 (4180): 947–948. Bibcode:1975Sci...187..947L. doi:10.1126/science.187.4180.947. PMID 17745279.
  4. Lawson, Douglas A. (16 May 1975). "Could Pterosaurs Fly?". Letters. Science. 188 (4189): 676–677. Bibcode:1975Sci...188..676G. doi:10.1126/science.188.4189.676. PMID 17755159.
  5. 1 2 Kellner, Alexander W. A.; Langston, Wann Jr. (5 June 1996). "Cranial remains of Quetzalcoatlus (Pterosauria, Azhdarchidae) from Late Cretaceous sediments of Big Bend National Park, Texas". Journal of Vertebrate Paleontology. 16 (2): 222–231. doi:10.1080/02724634.1996.10011310.
  6. Buffetaut, E.; Grigorescu, D.; Csiki, Z. (1 April 2002). "A new giant pterosaur with a robust skull from the latest Cretaceous of Romania". Naturwissenschaften. 89 (4): 180–184. Bibcode:2002NW.....89..180B. doi:10.1007/s00114-002-0307-1. PMID 12061403.
  7. 1 2 3 Witton, M.P., Martill, D.M. and Loveridge, R.F. (2010). "Clipping the Wings of Giant Pterosaurs: Comments on Wingspan Estimations and Diversity". Acta Geoscientica Sinica. 31: 79–81.CS1 maint: uses authors parameter (link)
  8. Henderson, Michael D.; Peterson, Joseph E. (30 March 2006). "An azhdarchid pterosaur cervical vertebra from the Hell Creek Formation (Maastrichtian) of southeastern Montana". Journal of Vertebrate Paleontology. 26 (1): 192–195. doi:10.1671/0272-4634(2006)26[192:AAPCVF]2.0.CO;2.
  9. Langston, Wann Jr. (1981). "Pterosaurs". Scientific American. 244 (2): 122–137. Bibcode:1981SciAm.244b.122L. doi:10.1038/scientificamerican0281-122. JSTOR 24964287.
  10. Guinness World Records 2014. The Jim Pattison Group. 2014. p. 27. ISBN 978-1-908843-15-9.
  11. Paul, Gregory S. (2002). Dinosaurs of the Air: The Evolution and Loss of Flight in Dinosaurs and Birds. Johns Hopkins University Press. p. 472. ISBN 0-8018-6763-0.
  12. 1 2 Witton, Mark P.; Habib, Michael B.; Laudet, Vincent (15 November 2010). "On the Size and Flight Diversity of Giant Pterosaurs, the Use of Birds as Pterosaur Analogues and Comments on Pterosaur Flightlessness". PLOS ONE. 5 (11): e13982. Bibcode:2010PLoSO...513982W. doi:10.1371/journal.pone.0013982. PMC 2981443. PMID 21085624.
  13. Andres, B.; Myers, T. S. (2013). "Lone Star Pterosaurs". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 103 (3–4): 1. doi:10.1017/S1755691013000303.
  14. 1 2 3 Lehman, T. M. (2001). "Late Cretaceous dinosaur provinciality". In Tanke, D. H.; Carpenter, K. (eds.). Mesozoic Vertebrate Life. Indiana University Press. pp. 310–328.
  15. Lehman, Thomas M.; Langston, Wann Jr. (September 1996). "Habitat and behavior of Quetzalcoatlus: paleoenvironmental reconstruction of the Javelina Formation (Upper Cretaceous), Big Bend National Park, Texas". Abstracts of Papers. Journal of Vertebrate Paleontology. 16 (Sup. 3): 48A. doi:10.1080/02724634.1996.10011371.
  16. Humphries, Stuart; Bonser, Richard H. C.; Witton, Mark P; Martill, David M (24 July 2007). "Did Pterosaurs Feed by Skimming? Physical Modelling and Anatomical Evaluation of an Unusual Feeding Method". PLOS Biology. 5 (8): e204. doi:10.1371/journal.pbio.0050204. PMC 1925135. PMID 17676976.
  17. MacCready, P. (1985). "The Great Pterodactyl Project" (PDF). Engineering & Science, California Institute of Technology. 49 (2): 18–24.
  18. 1 2 Henderson, Donald M. (18 May 2010). "Pterosaur body mass estimates from three-dimensional mathematical slicing" (PDF). Journal of Vertebrate Paleontology. 30 (3): 768–785. doi:10.1080/02724631003758334.
  19. Frazier, Reid (November 22, 2010). "Peerless Pterosaur Could Fly Long-Distance For Days". Morning Edition. NPR. Retrieved November 1, 2017.
  20. Padian, K. (1983). "A functional analysis of flying and walking in pterosaurs". Paleobiology. 9 (3): 218–239. doi:10.1017/S009483730000765X.
  21. Vincent, Mark (May 14, 2012). "Vintage Dinosaur Art: The evolution and ecology of the Dinosaurs: Part 2". Love in the Time of Chasmosaurs.
  22. Naish, Darren (August 20, 2013). "Quetzalcoatlus: the evil, pin-headed, toothy nightmare monster that wants to eat your soul". Tetrapod Zoology at Scientific American.
  23. "Engineers make dinosaurs fly". The Engineer. 22 June 2010. Archived from the original on May 13, 2014. Retrieved 26 September 2010.
  24. Jacobsen, Annie (February 27, 2011). "When Flying Dinosaurs Were Drones". Los Angeles Times Magazine. Archived from the original on March 8, 2013. Retrieved November 1, 2017.
  25. "UAS Advanced Development: Quetzalcoatlus Northropi". AeroVironment. 2011. Archived from the original on January 7, 2012. Retrieved July 28, 2011.


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