Compsognathus

Compsognathus
Temporal range: Late Jurassic, 150.8 Ma
Reconstruction of a skeleton, Museum of Ancient Life – Thanksgiving Point
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Dinosauria
Order: Saurischia
Suborder: Theropoda
Family: Compsognathidae
Subfamily: Compsognathinae
Cope, 1875
Genus: Compsognathus
Wagner, 1859
Type species
Compsognathus longipes
Wagner, 1859
Synonyms

Compsognathus corallestris
Bidar, Demay, & Thomel, 1972

Compsognathus (/kɒmpˈsɒɡnəθəs/;[1] Greek kompsos/κομψός; "elegant", "refined" or "dainty", and gnathos/γνάθος; "jaw")[2] is a genus of small, bipedal, carnivorous theropod dinosaurs. Members of its single species Compsognathus longipes could grow to the size of a turkey. They lived about 150 million years ago, the Tithonian age of the late Jurassic period, in what is now Europe. Paleontologists have found two well-preserved fossils, one in Germany in the 1850s and the second in France more than a century later. Today, C. longipes is the only recognized species, although the larger specimen discovered in France in the 1970s was once thought to belong to a separate species and named C. corallestris.

Many presentations still describe Compsognathus as "chicken-sized" dinosaurs because of the small size of the German specimen, which is now believed to be a juvenile. Compsognathus longipes is one of the few dinosaur species for which diet is known with certainty: the remains of small, agile lizards are preserved in the bellies of both specimens. Teeth discovered in Portugal may be further fossil remains of the genus.

Although not recognized as such at the time of its discovery, Compsognathus is the first theropod dinosaur known from a reasonably complete fossil skeleton. Until the 1990s, it was the smallest known non-avialan dinosaur; earlier it was incorrectly thought to be the closest relative of Archaeopteryx.

Compsognathus also holds the distinction of being the first dinosaur genus to be portrayed with feathers, by Thomas Henry Huxley in 1876.

Description

Size comparison of the French (orange) and German (green) specimens, with a human

For decades, Compsognathus were famed as the smallest dinosaurs known; the first specimen collected was around 1 m (3 ft) in length. However, dinosaurs discovered later, such as Caenagnathasia, Microraptor and Parvicursor, were even smaller. The largest Compsognathus specimen is estimated to have weighed somewhere between 0.83 and 3.5 kg (1.8 and 7.7 lb).[3][4]

Compsognathus were small, bipedal animals with long hind legs and longer tails, which they used for balance during locomotion. The forelimbs were smaller than the hindlimbs and featured three digits equipped with solid claws suited for grasping prey. Their delicate skulls were narrow and long, with tapered snouts. The skull had five pairs of fenestrae (skull openings), the largest of which was for the orbit (eye socket).[5] The eyes were large in proportion to the rest of the skull.

The lower jaw was slender and had no mandibular fenestra, a hole in the side of the lower jawbone commonly seen in archosaurs. The teeth were small but sharp, suited for its diet of small vertebrates and possibly other small animals, such as insects. Its frontmost teeth (those on the premaxilla) were unserrated, unlike those further back in the jaw which were flattened and more strongly recurved.[6] Scientists have used these dental characteristics to identify Compsognathus and its closest relatives.[7] Reisdorf and Wuttke (2012) described the taphonomical phenomena of the German specimen of Compsognathus.[8]

The Compsognathus specimen discovered in Germany in the 19th century featured only two digits on each forelimb, leading scientists to conclude that this was how the creature appeared in life.[9] However, the fossil discovered later in France revealed the manus (hands) to have had three digits,[10] similar to other members of compsognathid genera. The fossilization of the German Compsognathus had simply failed to preserve the specimen's hands completely. Bidar supposed that the French specimen had webbed hands, which would look like flippers in life.[11] In the 1975 book The Evolution and Ecology of the Dinosaurs, L. B. Halstead depicts the animal as an amphibious dinosaur capable of feeding on aquatic prey and swimming out of reach of larger predators.[12] Ostrom debunked this hypothesis[9] by showing conclusively that the French specimen was nearly identical to the German specimen in every aspect but its size. Peyer confirmed these conclusions.[13]

Integument

Evidence from related species suggests that the body might have been covered with feather-like structures.

Some relatives of Compsognathus, namely Sinosauropteryx and Sinocalliopteryx, have been preserved with the remains of simple feathers covering the body like fur,[14] promoting some scientists to suggest that Compsognathus might have been feathered in a similar way.[15] Consequently, many depictions of Compsognathus show them with coverings of downy proto-feathers. However, no feathers or feather-like covering have been preserved with Compsognathus fossils, in contrast to Archaeopteryx, which are found in the same sediments. Karin Peyer, in 2006, reported skin impressions preserved on the side of the tail starting at the 13th tail vertebra. The impressions showed small bumpy tubercles, similar to the scales found on the tail and hind legs of Juravenator.[16] Additional scales had in 1901 been reported by Von Huene, in the abdominal region of the German Compsognathus, but Ostrom subsequently disproved this interpretation;[9][17] in 2012 they were by Achim Reisdorf seen as plaques of adipocere, corpse wax.[8]

Like Compsognathus, and unlike Sinosauropteryx, a patch of fossilized skin from the tail and hindlimb of the possible relative Juravenator starki shows mainly scales, though there is some indication that simple feathers were also present in the preserved areas.[18] This may mean that a feather covering was not ubiquitous in this group of dinosaurs.[19]

Discovery and species

Joseph Oberndorfer acquired this fossil in Bavaria, Germany, in 1859. Shown here is a cast at the Bavarian State Institute for Paleontology and Historical Geology

Compsognathus is known from two almost complete skeletons, one from Germany that is 89 cm (35 in) long and another from France that is 125 cm (49 in) long.[20] The physician and fossil collector Joseph Oberndorfer acquired the German specimen (BSP AS I 563) in 1859, discovered about the same year in the lithographic limestone deposits in the Riedenburg-Kelheim region of Bavaria, in the Jurassic part of a lagoonal region known as the Solnhofen archipelago.[21] The limestone of this area has also yielded such well-preserved fossils as Archaeopteryx with feather impressions and some pterosaurs with imprints of their wing membranes. The German Compsognathus fossil itself most likely came from the Painten Formation of the Kapfelberg locality, specifically dated to the uppermost Kimmeridgian stage (150.8 million years ago);[8] however, alternative possibilities include quarries near Jachenhausen[22] or Goldberg, both from the Tithonian, to which stage Compsognathus has traditionally been dated.[8] Johann A. Wagner discussed the specimen briefly in 1859, when he coined the name Compsognathus longipes,[23] and described it in detail in 1861.[24] In early 1868, Thomas Huxley compared the two species and, following earlier suggestions by Karl Gegenbaur[25] and Edward Drinker Cope,[26] concluded that, apart from its arms and feathers, the Archaeopteryx skeleton was closely similar to Compsognathus, and that the proto-bird was related to the dinosaurs.[27][28] In 1896, Othniel Marsh recognized the fossil as a true member of the Dinosauria.[29] John Ostrom thoroughly redescribed the species in 1978, making it one of the best-known small theropods at that time.[9] The German specimen is on display at the Bayerische Staatsammlung für Paläontologie und historische Geologie (Bavarian State Institute for Paleontology and Historical Geology) in Munich, Germany, which bought the fossil from Oberndorfer in 1865.[21]

The fossil from Canjuers, France

The larger French specimen (MNHN CNJ 79) was discovered by quarry owner Louis Ghirardi around 1971 in the Portlandian lithographic limestone of Canjuers near Nice in southeastern France.[13] It dates to the lower Tithonian. Although Alain Bidar originally described the specimen as a separate species called Compsognathus corallestris,[11] Ostrom, Jean-Guy Michard and others have since relabeled it as another example of Compsognathus longipes.[13][30] Quimby identified the smaller German specimen as a juvenile of the same species.[31] In 1983, the National Museum of Natural History in Paris acquired the French Compsognathus fossil; Michard thoroughly studied it there.[30]

Collector Heinrich Fischer had originally labeled a partial foot, from the Solnhofen area, as belonging to Compsognathus longipes. Though this identification was rejected by Wilhelm Barnim Dames in 1884,[32] Friedrich von Huene nevertheless in 1925 provisionally referred the specimen to Compsognathus.[33] However, Ostrom's study of 1978 has disproven this. Jens Zinke in 1998 assigned forty-nine teeth from the Kimmeridgian Guimarota formation of Portugal to the genus. These were not identical to those of C. longipes, having serrations on the front edge, but were because of general similarities in form referred to a Compsognathus sp.[34]

In 1997 Virginia Morell renamed a related Chinese form, Sinosauropteryx prima, into a Compsognathus prima;[35] this has found no general acceptance.

Classification

Modern restoration of the two skeletons
Skeletal reconstruction by Marsh, 1896

The genus Compsognathus gives its name to the family Compsognathidae, a group composed mostly of small dinosaurs from the late Jurassic and early Cretaceous periods of China, Europe and South America.[13] For many years it was the only member known; however in recent decades paleontologists have discovered several related genera. The clade includes Aristosuchus,[36] Huaxiagnathus,[37] Mirischia,[38] Sinosauropteryx,[14][39] and perhaps Juravenator[40] and Scipionyx.[41] At one time, Mononykus was proposed as a member of the family, but this was rejected by Chen and coauthors in a 1998 paper; they considered the similarities between Mononykus and the compsognathids to be an example of convergent evolution.[7] The position of Compsognathus and its relatives within the coelurosaur group is uncertain. Some, such as theropod expert Thomas Holtz Jr. and co-authors Ralph Molnar and Phil Currie in the landmark 2004 text Dinosauria, hold the family as the most basal of the coelurosaurs,[42] while others as part of the Maniraptora.[43][44]

For almost a century, Compsognathus longipes was the only well-known small theropod species. This led to comparisons with Archaeopteryx and to suggestions of an especially close relationship with birds. In fact, Compsognathus, rather than Archaeopteryx, piqued Huxley's interest in the origin of birds.[45] The two animals share similarities in shape and proportions, so many in fact that two specimens of Archaeopteryx, the "Eichstätt" and the "Solnhofen", were for a time misidentified as those of Compsognathus.[5] Many other types of theropod dinosaurs, such as maniraptorans, are now known to have been more closely related to birds.[46]

Below is a simplified cladogram placing Compsognathus in Compsognathidae by Senter et al. in 2012.[47]

Compsognathidae


Sinocalliopteryx



Huaxiagnathus





Sinosauropteryx




Compsognathus




Juravenator



Scipionyx






Paleobiology

In a 2001 study conducted by Bruce Rothschild and other paleontologists, nine foot bones referred to Compsognathus were examined for signs of stress fracture, but none were found.[48]

Diet

This 1903 illustration by Franz Nopcsa von Felső-Szilvás shows the gastric content of the German specimen

The remains of a lizard in the German specimen's thoracic cavity show that Compsognathus preyed on small vertebrates.[7] Marsh, who examined the specimen in 1881, thought that this small skeleton in the Compsognathus belly was an embryo, but in 1903, Franz Nopcsa concluded that it was a lizard.[49] Ostrom identified the remains as belonging to a lizard of the genus Bavarisaurus,[50] which he concluded was a fast and agile runner owing to its long tail and limb proportions. This in turn led to the conclusion that its predators, Compsognathus, must have had sharp vision and the ability to rapidly accelerate and outrun the lizard.[9] The Bavarisaurus is in a single piece, indicating that the Compsognathus must have swallowed its prey whole. The French specimen's gastric contents consist of unidentified lizards or sphenodontids.[13]

Possible eggs

The plate of the German Compsognathus shows several circular irregularities 10 mm (0.39 in) in diameter near the skeletal remains. Peter Griffiths interpreted them as immature eggs in 1993.[51] However, later researchers have doubted their connection to the genus because they were found outside the body cavity of the animal. A well-preserved fossil of a Sinosauropteryx, a genus related to Compsognathus, shows two oviducts bearing two unlaid eggs. These proportionally larger and less numerous eggs of Sinosauropteryx cast further doubt on the original identification of the purported Compsognathus eggs.[7] In 1964 German geologist Karl Werner Barthel had explained the discs as gas bubbles formed in the sediment because of the putrefaction of the carcass.[52]

Paleoecology

Restoration of Archaeopteryx chasing a juvenile Compsognathus

During the late Jurassic, Europe was a dry, tropical archipelago at the edge of the Tethys Sea. The fine limestone in which the skeletons of Compsognathus have been found originated in calcite from the shells of marine organisms. Both the German and French areas where Compsognathus specimens have been preserved were lagoons situated between the beaches and coral reefs of the Jurassic European islands in the Tethys Sea.[53] Contemporaries of Compsognathus longipes include the early avialan Archaeopteryx lithographica and the pterosaurs Rhamphorhynchus muensteri and Pterodactylus antiquus. The same sediments in which Compsognathus have been preserved also contain fossils of a number of marine animals such as fish, crustaceans, echinoderms and marine mollusks, confirming the coastal habitat of this theropod. No other dinosaur has been found in association with Compsognathus, indicating that these little dinosaurs might in fact have been the top land predator in these islands.[46]

Children's dinosaur books commonly feature Compsognathus. For a long time they were unique in their small size, as most other small dinosaurs were discovered and described a century or more later.[54][55] These animals have appeared in the movies The Lost World: Jurassic Park and Jurassic Park III. In The Lost World: Jurassic Park, one of the characters incorrectly identifies the species as "Compsognathus triassicus", combining the genus name of Compsognathus longipes with the specific name of Procompsognathus triassicus, a distantly related small carnivore featured in the Jurassic Park novels.[56]

References

  1. "Compsognathus", Oxford English Dictionary, Second Edition
  2. Liddell, Henry George; Scott, Robert (1980) [1871]. A Greek-English Lexicon (abridged ed.). Oxford, United Kingdom: Oxford University Press. ISBN 0-19-910207-4.
  3. Therrien, F.; Henderson, D.M. (2007). "My theropod is bigger than yours...or not: estimating body size from skull length in theropods". Journal of Vertebrate Paleontology. 27 (1): 108–115. doi:10.1671/0272-4634(2007)27[108:MTIBTY]2.0.CO;2.
  4. Seebacher, F. (2001). "A new method to calculate allometric length-mass relationships of dinosaurs". Journal of Vertebrate Paleontology. 21 (1): 51–60. doi:10.1671/0272-4634(2001)021[0051:ANMTCA]2.0.CO;2.
  5. 1 2 Lambert, David (1993). The Ultimate Dinosaur Book. New York: Dorling Kindersley. pp. 38–81. ISBN 1-56458-304-X.
  6. Stromer, E., 1934, "Die Zähne des Compsognathus und Bemerkungen über das Gebiss der Theropoda", Zentralblatt für Mineralalogie, Geologie und Paläontologie, Abteilung B, Jahrgang 1934: 74–85
  7. 1 2 3 4 Chen, P.; Dong, Z.; Zhen, S. (1998). "An exceptionally well-preserved theropod dinosaur from the Yixian Formation of China". Nature. 391 (6663): 147–152. Bibcode:1998Natur.391..147C. doi:10.1038/34356.
  8. 1 2 3 4 Reisdorf, A.G.; Wuttke, M. (2012). "Re-evaluating Moodie's Opisthotonic-Posture Hypothesis in fossil vertebrates. Part I: Reptiles - The taphonomy of the bipedal dinosaurs Compsognathus longipes and Juravenator starki from the Solnhofen Archipelago (Jurassic, Germany)". Palaeobiodiversity and Palaeoenvironments. 92 (1): 119–168. doi:10.1007/s12549-011-0068-y.
  9. 1 2 3 4 5 Ostrom, J.H. (1978). "The osteology of Compsognathus longipes". Zitteliana. 4: 73–118.
  10. Gauthier, J.; Gishlick A.D. (2000). "Re-examination of the manus of Compsognathus and its relevance to the original morphology of the Coelurosaur manus". Journal of Vertebrate Paleontology. 20 (3, Supplement): 43A. doi:10.1080/02724634.2000.10010765.
  11. 1 2 Bidar, A.; Demay L.; Thomel G. (1972). "Compsognathus corallestris, une nouvelle espèce de dinosaurien théropode du Portlandien de Canjuers (Sud-Est de la France)". Annales du Muséum d'Histoire Naturelle de Nice. 1: 9–40.
  12. Halstead L.B. (1975). The evolution and ecology of the dinosaurs. Eurobook. ISBN 0-85654-018-8.
  13. 1 2 3 4 5 Peyer, K. (2006). "A Reconsideration Of Compsognathus From The Upper Tithonian Of Canjuers, Southeastern France". Journal of Vertebrate Paleontology. 26 (4): 879–896. doi:10.1671/0272-4634(2006)26[879:AROCFT]2.0.CO;2.
  14. 1 2 Currie, P.J.; P. Chen (2001). "Anatomy of Sinosauropteryx prima from Liaoning, northeastern China". Canadian Journal of Earth Sciences. 38 (12): 1705–1727. Bibcode:2001CaJES..38.1705C. doi:10.1139/cjes-38-12-1705.
  15. Ji, S.; Ji, Q.; Lu, J.; Yuan, C. (2007). "A new giant compsognathid dinosaur with long filamentous integuments from Lower Cretaceous of Northeastern China". Acta Geologica Sinica. 81 (1): 8–15.
  16. Peyer, K. (2006). "A reconsideration of Compsognathus from the Upper Tithonian of Canjuers, southeastern France". Journal of Vertebrate Paleontology. 26 (4): 879–896. doi:10.1671/0272-4634(2006)26[879:AROCFT]2.0.CO;2.
  17. von Huene, F. (1901). "Der vermuthliche Hautpanzer des "Compsognathus longipes" Wagner". Neues Jahrbuch für Mineralogie, Geologie and Palaeontologie. 1: 157–160.
  18. Goehlich, U.B.; Tischlinger, H.; Chiappe, L.M. (2006). "Juraventaor starki (Reptilia, Theropoda) ein nuer Raubdinosaurier aus dem Oberjura der Suedlichen Frankenalb (Sueddeutschland): Skelettanatomie und Wiechteilbefunde". Archaeopteryx. 24: 1–26.
  19. Xu, Xing (2006). "Palaeontology: Scales, feathers and dinosaurs". Nature. 440 (7082): 287–8. Bibcode:2006Natur.440..287X. doi:10.1038/440287a. PMID 16541058.
  20. Paul, Gregory S. (1988). "Early Avetheropods". Predatory Dinosaurs of the World. New York: Simon & Schuster. pp. 297–300. ISBN 0-671-61946-2.
  21. 1 2 Wellnhofer, P. (2008). "Dinosaurier". Archaeopteryx — der Urvogel von Solnhofen. Munich: Verlag Dr. Friedrich Pfeil. p. 256. ISBN 978-3-89937-076-8.
  22. Mäuser M. 1983, "Neue Gedanken über Compsognathus longipes WAGNER und dessen Fundort", In: Erwin Rutte-Festschrift, Weitenburger Akademie, pp 157–162
  23. Wagner, J. A. (1859). "Über einige im lithographischen Schiefer neu aufgefundene Schildkröten und Saurier". Gelehrte Anzeigen der Bayerischen Akademie der Wissenschaften. 49: 553.
  24. Wagner, Johann Andreas (1861). "Neue Beiträge zur Kenntnis der urweltlichen Fauna des lithographischen Schiefers; V. Compsognathus longipes Wagner". Abhandlungen der Bayerischen Akademie der Wissenschaften. 9: 30–38.
  25. Gegenbaur, Karl (1863). "Vergleichend-anatomische Bemerkungen über das Fußskelet der Vögel". Archiv für Anatomie, Physiologie und Wissenschaftliche Medicin. 1863: 450–472.
  26. Cope, Edward Drinker (1867). "An account of the extinct reptiles which approached the birds". Proceedings of the Academy of Natural Sciences of Philadelphia. 19: 234–235.
  27. Huxley, T.H. (1868). "On the animals which are most nearly intermediate between birds and reptiles". Annals and Magazine of Natural History. 2: 66–75.
  28. Foster, Michael; Lankester, E. Ray 1898–1903. The scientific memoirs of Thomas Henry Huxley. 4 vols and supplement, London: Macmillan.
  29. Marsh, Othniel Charles (1896). "Classification of dinosaurs". Geological Magazine. 3 (9): 388–400. doi:10.1017/S0016756800131826.
  30. 1 2 Michard, J. G. (1991). "Description du Compsognathus (Saurischia, Theropoda) de Canjuers (Jurassique supérieur du Sud-est de la France), position phylogénétique, relation avec Archaeopteryx et implications sur l'origine théropodienne des oiseaux,". Ph.D. dissertation, Muséum National d'Histoire Naturelle, Paris.
  31. Callison, G.; H. M. Quimby (1984). "Tiny dinosaurs: Are they fully grown?". Journal of Vertebrate Paleontology. 3 (4): 200–209. doi:10.1080/02724634.1984.10011975.
  32. Dames, W.B., 1884, "Vorlegung der Metatarsen eines Compsognathus-ähnlichen Reptils von Solenhofen", Sitzungsberichte der Gesellschaft Naturforschender Freunde zu Berlin, Jahrgang 1884, pp. 179-180
  33. Huene, F.R., von, 1925, "Eine neue Rekonstruktion von Compsognathus longipes", Zentralblatt für Mineralogie, Geologie und Palaeontologie Jahrgang 1925, Abteilung B(5): 157-160
  34. Zinke, J. (1998). "Small theropod teeth from the Upper Jurassic coal mine of Guimarota (Portugal)". Palaontologische Zeitschrift. 72: 179–189. doi:10.1007/bf02987825.
  35. Morell, V. (1997). "The origin of birds: the dinosaur debate". Audubon Magazine. 99 (2): 36–45.
  36. Seeley, H.G. (1887). "On Aristosuchus pusillus (Owen), being further notes on the fossils described by Sir. R. Owen as Poikilopleuron pusillus, Owen". Quarterly Journal of the Geological Society of London. 43: 221–228. doi:10.1144/GSL.JGS.1887.043.01-04.22.
  37. Hwang, S.H.; Norell, M. A.; Qiang, J.; Keqin, G. (2004). "A large compsognathid from the Early Cretaceous Yixian Formation of China". Journal of Systematic Paleontology. 2: 13–39. doi:10.1017/S1477201903001081.
  38. Naish, D.; Martill, D. M.; Frey, E. (2004). "Ecology, systematics and biogeographical relationships of dinosaurs, including a new theropod, from the Santana Formation (?Albian, Early Cretaceous) of Brazil". Historical Biology. 16 (2–4): 1–14. doi:10.1080/08912960410001674200.
  39. Ji, Q.; Ji S.A. (1996). "On discovery of the earliest bird fossil in China and the origin of birds (in Chinese)". Chinese Geology. 233: 30–33.
  40. Göhlich, U.; L. M Chiappe (2006). "A new carnivorous dinosaur from the Late Jurassic Solnhofen archipelago". Nature. 440 (7082): 329–332. Bibcode:2006Natur.440..329G. doi:10.1038/nature04579. PMID 16541071.
  41. Dal Sasso, C.; M. Signore (1998). "Exceptional soft-tissue preservation in a theropod dinosaur from Italy". Nature. 392 (6674): 383–387. Bibcode:1998Natur.392..383D. doi:10.1038/32884.
  42. Holtz TR, Molnar RE, Currie PJ (2004). "Basal Tetanurae". In Weishampel DB, Osmólska H, Dodson P. The Dinosauria (2nd Edition). University of California Press. p. 105. ISBN 0-520-24209-2.
  43. Gauthier, J.A. (1986). "Saurischian monophyly and the origin of birds". In Padian, K. (ed.) the Origin of Birds and the Evolution of Flight, Memoirs of the California Academy of Sciences. 8: 1–55.
  44. Forster, C.A.; Sampson, S.D.; Chiappe, L.M.; Krause, D.W. (1998). "The theropod ancestry of birds: new evidence from the Late Cretaceous of Madagascar". Science. 279 (5358): 1915–1919. Bibcode:1998Sci...279.1915F. doi:10.1126/science.279.5358.1915. PMID 9506938.
  45. Fastovsky DE, Weishampel DB (2005). "Theropoda I:Nature red in tooth and claw". In Fastovsky DE, Weishampel DB. The Evolution and Extinction of the Dinosaurs (2nd Edition). Cambridge University Press. pp. 265–299. ISBN 0-521-81172-4.
  46. 1 2 Weishampel, D.B., Dodson, P., Oslmolska, H. (2004). The Dinosauria (Second ed.). University of California Press.
  47. Senter, P.; Kirkland, J. I.; Deblieux, D. D.; Madsen, S.; Toth, N. (2012). Dodson, Peter, ed. "New Dromaeosaurids (Dinosauria: Theropoda) from the Lower Cretaceous of Utah, and the Evolution of the Dromaeosaurid Tail". PLoS ONE. 7 (5): e36790. Bibcode:2012PLoSO...736790S. doi:10.1371/journal.pone.0036790. PMC 3352940Freely accessible. PMID 22615813.
  48. Rothschild, B., Tanke, D. H., and Ford, T. L., 2001, Theropod stress fractures and tendon avulsions as a clue to activity: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, p. 331-336.
  49. Nopcsa, Baron F. (1903). "Neues ueber Compsognathus". Neues Jahrbuch fur Mineralogie, Geologie und Palaeontologie (Stuttgart). 16: 476–494.
  50. Evans, S.E. (1994). "The Solnhofen (Jurassic: Tithonian) lizard genus Bavarisaurus: new skull material and a reinterpretation". Neues Jahrbuch für Paläontologie und Geologie, Abhandlungen. 192: 37–52.
  51. Griffiths, P. (1993). "The question of Compsognathus eggs". Revue de Paleobiologie Spec. 7: 85–94.
  52. Barthel, K.W. (1964). "Zur Entstehung der Solnhofener Plattenkalke (unteres Untertithon)". Mitteilungen der Bayerischen Staatssammlung für Paläontologie und historische Geologie. 4: 7–69.
  53. Viohl G (1985). "Geology of the Solnhofen lithographic limestone and the habitat of Archaeopteryx". In Hecht MK, Ostrom JH, Viohl G, Wellnhofer P. The Beginnings of Birds: Proceedings of the International Archaeopteryx Conference. Eichstätt: Freunde des Jura-Museums. pp. 31–44. OCLC 13213820.
  54. Wilson, Ron (1986). 100 Dinosaurs from A to Z. New York: Grosset & Dunlap. p. 18. ISBN 0-448-18992-5.
  55. Attmore, Stephen (1988). Dinosaurs. Newmarket, England: Brimax Books. p. 18. ISBN 0-86112-460-X.
  56. Berry, Mark F. (2002). The dinosaur filmography. Jefferson, North Carolina: McFarland. p. 273. ISBN 0-7864-1028-0.
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