Compsognathus (/kɒmpˈsɒɡnəθəs/;[1]Greekkompsos/κομψός; "elegant", "refined" or "dainty", andgnathos/γνάθος; "jaw")[2] is agenus of small,bipedal,carnivoroustheropoddinosaur. Members of its singlespeciesCompsognathus longipes could grow to around the size of achicken. They lived about 150 million years ago, during theTithonianage of the lateJurassicperiod, in what is nowEurope. Paleontologists have found two well-preservedfossils, one inGermany in the 1850s and the second inFrance more than a century later. Today,C. longipes is the only recognized species, although the French specimen was once thought to belong to a separate species namedC. corallestris.
Many presentations still describeCompsognathus as "chicken-sized" dinosaurs because of the size of the German specimen, which is now believed to be a juvenile.Compsognathus longipes is one of the few dinosaur species whose 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, with the preceding centuries incorrectly labelling it as the closest relative ofArchaeopteryx.
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.[3] The German specimen (specimen number BSP AS I 563) stems from limestone deposits inBavaria and was part of the collection of physician andfossil collector Joseph Oberndorfer. Oberndorfer lent the specimen to paleontologistJohann A. Wagner, who published a brief discussion in 1859, where he coined the nameCompsognathus longipes.[4] Wagner did not recogniseCompsognathus as a dinosaur, but instead described it as one of the "most curious forms among the lizards".[4][5] He published a more detailed description in 1861.[6] In 1866, Oberndorfer's collection, including theCompsognathus specimen, was acquired by the paleontological state collection inMunich.[7]
The year of discovery and the exact locality of the German specimen are unknown, possibly because Oberndorfer did not reveal details of the discovery to prevent other collectors from exploiting the locality;[7] later authors have suggested that the German specimen was probably discovered during the 1850s. Weathering of the slab on which the fossil is preserved indicates that it was collected from a pile of waste rock left behind by quarrying.[8] The specimen either stems from Jachenhausen or the region Riedenburg–Kehlheim.[8][9] All possible localities are part of lagoonal deposits of thePainten Formation, and date to the latest part of the lateKimmeridgian or the earlier part of the earlyTithonian.[8] In the Jurassic, the region was part of the Solnhofen archipelago. The limestone of the area, theSolnhofen limestone, had been quarried for centuries, and yielded such well-preserved fossils asArchaeopteryx with feather impressions andpterosaurs with imprints of their wing membranes.[10]
In two publications in 1868 and 1870,Thomas Huxley, a major proponent ofCharles Darwin's theory of evolution, comparedCompsognathus withArchaeopteryx, which was considered the earliest known bird. Following earlier suggestions byCarl Gegenbaur[11] andEdward Drinker Cope,[12] Huxley found thatArchaeopteryx was closely similar toCompsognathus, and referred to the latter as a "bird-like reptile". He concluded thatbirds must have evolved from dinosaurs, an assessment that establishedCompsognathus as one of the most widely known dinosaurs.[5][13][14] The specimen has since been studied by many prominent paleontologists, includingOthniel Charles Marsh, who visited Munich in 1881. The German paleontologistJ.G. Baur, who worked as an assistant of Marsh, removed the right ankle from the slab for illustration and study; this removed part got lost since.[5][15] Although Baur published a detailed study of the ankle in 1882, which is now the only available source of information of this part of the skeleton, his reconstruction was later found to be inconsistent with corresponding impressions on the slab.[5]John Ostrom thoroughly described the German specimen as well as the newly discovered French specimen in 1978, makingCompsognathus one of the best-known small theropods at that time.[5] He also concluded that the German specimen likely belongs to an immature individual.[5]
The fossil from Canjuers, France
The larger French specimen (Y85R M4M) was discovered in around 1971 in thePortlandian lithographic limestone ofCanjuers nearNice.[16] It dates to the lower Tithonian, as indicated byammoniteindex fossils. As Solnhofen, Canjures was famous for its limestone plates, which were quarried and sold under the name "dalles de Provence". The specimen was originally part of a large private fossil collection of Louis Ghirardi, the owner of the Canjures quarries. The collection, including theCompsognathus specimen, was sold to theNational Museum of Natural History inParis in 1983. Alain Bidar and Gérard Thomel, in a brief 1972 description, announced the new find under a separate species,Compsognathus corallestris.[17] A more comprehensive description followed in the same year.[18] According to these authors, the new species differed from the German species in its larger size and modified, flipper-like hand. Ostrom, Jean-Guy Michard and others have since relabeled it as another example ofCompsognathus longipes.[16][19] In 1984, George Callison and Helen Quimby identified the smaller German specimen as a juvenile of the same species.[19][20]
Collector Heinrich Fischer had originally labeled a partial foot consisting of three metatarsals and a phalanx, from theSolnhofen area, as belonging toCompsognathus longipes. This identification was rejected by Wilhelm Dames, when he described the specimen for the first time in 1884.[21]Friedrich von Huene, in 1925 and 1932, also found that the foot did probably not belong toCompsognathus itself but to a closely related genus.[22][23]: 336 Ostrom, in his 1978 monography, questioned the attribution of this fossil toCompsognathus once more.[5] Jens Zinke, in 1998, assigned forty-nine isolated teeth from theGuimarota coal mine ofPortugal to the genus. Zinke found that these teeth are not identical to those ofCompsognathus longipes, having serrations on the front edge, and thus labeled the teeth asCompsognathus sp. (of unknown species).[24]
Size comparison of the French (orange) and German (green) specimens, with a human
For decades,Compsognathus was known as thesmallest known non-avian dinosaur,[5] although some dinosaurs discovered later, such asMahakala andMicroraptor, were even smaller.[25][26] The German specimen was estimated to be 70–75 cm (28–30 in)[5] and 89 cm (35 in)[3] in length by separate authors, while the larger French specimen was estimated at 1.25 m (4 ft 1 in)[3] and 1.4 m (4 ft 7 in)[16] in length. The height at the hip has been estimated at 20 cm (7.9 in) for the German specimen and at 29 cm (11 in) for the French specimen.[3] The German specimen was estimated to have weighed 0.32 kg (0.71 lb)[27] and 0.58 kg (1.3 lb),[3] and the French specimen 2.5 kg (5.5 lb)[3] and 3.5 kg (7.7 lb).[28] Compared to other compsognathids, the larger French specimen would have been similar in size to largerSinosauropteryx specimens, but smaller thanHuaxiagnathus andMirischia.[16]
Compsognathus were small, bipedal animals with long legs and longer tails, which they used for balance during locomotion. The forelimbs were smaller than the hindlimbs. The hand bore two large, clawed digits and a third, smaller digit that may have been non-functional.[16][29] Their delicate skulls were narrow and long, with tapered snouts. The skull had five pairs offenestrae (skull openings), the largest of which was for theorbit (eye socket),[30] with the eyes being larger 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 inarchosaurs.
The teeth were small and pointed, suited for its diet of small vertebrates and possibly other small animals, such as insects. The German specimen had three teeth in eachpremaxilla (front bone of the lower jaw), 15 or 16 teeth in each maxilla, and 18 teeth in the lower jaw.[5][31] The French specimen had more teeth, including four in each premaxilla, 17 or 18 in the maxilla, and at least 21 teeth in the dentary.[16] Compsognathids were unique among theropods in havingtooth crowns that curved backwards at two thirds of their height, while their mid-parts were straight; also, the crowns had expanded bases.[16] InCompsognathus, the frontmost teeth of the upper and lower jaws wereunserrated, while those further back had fine serrations on their rear edges. In the German specimen, the crowns were around two times higher than wide in the front of the jaws but diminished in height further back, with the last tooth about as high as wide.[31] The German specimen also shows adiastema (tooth gap) behind the first three teeth of the premaxilla.[5] As such a gap was not present in the French specimen, Peyer suggested that additional teeth were possibly present in this region the German specimen.[16]
The number of digits on the hand ofCompsognathus has been a source of debate.[29] For much of its history,Compsognathus was typically depicted with three digits, as is typical for theropods.[5][29] However, the type specimen only preserved phalanges from the first two digits, leading to the suggestion thatCompsognathus had only two functional digits, with the third metacarpal being smaller and thinner.[5] Study of the French specimen indicated that the third digit bore at least one or two small phalanges.[16][29] However, there remains no evidence for an ungual phalanx on the third digit, so the digit may have been reduced and non-functional.[29]
Evidence from related species suggests that the body might have been covered with feather-like structures.
Some relatives ofCompsognathus, namelySinosauropteryx andSinocalliopteryx, have been preserved with the remains of simple feathers covering the body like fur,[32] prompting some scientists to suggest thatCompsognathus might have been feathered in a similar way.[33] Consequently, many depictions ofCompsognathus show them with coverings of downy proto-feathers. However, no feathers or feather-like covering have been preserved withCompsognathus fossils, in contrast toArchaeopteryx, 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 ofJuravenator.[34] A 2022 review of non-feather integument of non-avialan theropods interprets these structures as aberrant bony growths rather than scales, as the structures are "texturally and mineralogically indistinguishable" from the rest of the fossilized vertebrae.[35] Additional scales had in 1901 been reported by Von Huene, in the abdominal region of the GermanCompsognathus, but Ostrom subsequently disproved this interpretation;[5][36] in 2012, Achim Reisdorf postulated that they are plaques ofadipocere, corpse wax.[8]
A patch of fossilized skin from the tail and hindlimb of the possible relativeJuravenator starki shows mainly scales, though there is some indication that simple feathers were also present in the preserved areas.[37] This may mean that a feather covering was not ubiquitous in this group of dinosaurs, or maybe that some species had fewer feathers than others.[38]
Originally classified as a lizard, the dinosaurian affinities ofCompsognathus were first noted by Gegenbaur, Cope, and Huxley between 1863 and 1868.[11][12][13] Cope, in 1870, classifiedCompsognathus within a new clade of dinosaurs, the Symphypoda, which also containedOrnithotarsus (today classified asHadrosaurus).[39][40] Later, both genera were found to belong to other groups of Cope's classification of dinosaurs:Compsognathus to the Gonipoda (equivalent toTheropoda, in which it is now classified), andOrnithotarsus to the Orthopoda (equivalent toOrnithischia).[40] Huxley, in 1870, rejected Cope's dinosaur classification scheme, and instead proposed the new cladeOrnithoscelida, in which he included the Dinosauria (comprising several forms now considered as ornithischians) and another new clade, the Compsognatha, which containedCompsognathus as the only member.[41][42] Later, these groups fell into disuse, although a resurrection of the Ornithoscelida was proposed in 2017.[43] The group Compsognatha was used for the last time by Marsh in a 1896 publication, where it was treated as a suborder of Theropoda.[16][44] In the same publication, Marsh erected the new familyCompsognathidae.[16][44] Friedrich von Huene, in 1914, erected the newinfraorderCoelurosauria, which includes the Compsognathidae amongst other families of small theropods; this classification remained in use since.[16][45]
The Compsognathidae are a group of mostly small dinosaurs from the late Jurassic and earlyCretaceous periods of China, Europe and South America.[16] For many years,Compsognathus was the only member known, but in recent decades paleontologists have discovered several related genera. Theclade includesAristosuchus,[46]Huaxiagnathus,[47]Mirischia,[48]Sinosauropteryx,[32][49] and perhapsJuravenator andScipionyx.[50][51] 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 betweenMononykus and the compsognathids to be an example ofconvergent evolution.[52] The position ofCompsognathus and its relatives within thecoelurosaur group is uncertain. Some, such as theropod expertThomas Holtz Jr. and co-authorsRalph Molnar andPhil Currie in the landmark 2004 textDinosauria, hold the family as the mostbasal of the coelurosaurs,[53] while others as part of theManiraptora.[54][55]
For almost a century,Compsognathus longipes was the only well-known small theropod species. This led to comparisons withArchaeopteryx and to suggestions of an especially close relationship with birds. In fact,Compsognathus, rather thanArchaeopteryx, piqued Huxley's interest in the origin of birds.[56] The two animals share similarities in shape and proportions, so many in fact that two specimens ofArchaeopteryx, the "Eichstätt" and the "Solnhofen", were for a time misidentified as those ofCompsognathus.[30] Many other types of theropod dinosaurs, such asmaniraptorans, are now known to have been more closely related to birds.[57]
Skeletal reconstruction by Marsh, 1896Diagrams showing known elements of the two specimens (middle) and othercompsognathids
Below is a simplified cladogram placingCompsognathus in Compsognathidae by Senter et al. in 2012.[58]
In a 2001 study conducted by Bruce Rothschild and other paleontologists, nine foot bones referred toCompsognathus were examined for signs ofstress fracture, but none were found.[59]
Bidar and colleagues, in their 1972 description of the French specimen, argued that this specimen had webbed hands which would look like flippers in life. This interpretation was based on a supposed impression of the flipper that consists of several undulating wrinkles running parallel to the forelimb on the surface of the slab.[18] In a 1975 popular book,L. Beverly Halstead depicts the animal as an amphibious dinosaur capable of feeding on aquatic prey and swimming out of reach of larger predators.[60] Ostrom debunked this hypothesis, noting that the forelimb of the French specimen is poorly preserved, and that the wrinkles extend well beyond the skeleton and thus are likely sedimentary structures unrelated to the fossil.[5][16]
The remains of a lizard in the German specimen's thoracic cavity show thatCompsognathus preyed on small vertebrates.[52] Marsh, who examined the specimen in 1881, thought that this small skeleton in theCompsognathus belly was an embryo, but in 1903,Franz Nopcsa concluded that it was a lizard.[61] Ostrom identified the remains as belonging to a lizard of the genusBavarisaurus,[62] 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.[5] Conrad made the lizard found in the thoracic cavity of the German specimen ofCompsognathus theholotype of a new speciesSchoenesmahl dyspepsia.[63] The lizard is in several pieces, indicating that theCompsognathus must have dismembered it while restraining it with its hands and teeth, and then swallowed the remains whole; a similar strategy is used by modern predatory birds.[63] The French specimen's gastric contents consist of unidentified lizards orsphenodontids.[16]
The plate of the GermanCompsognathus shows several circular irregularities 10 mm (0.39 in) in diameter near the skeletal remains. Peter Griffiths interpreted them as immature eggs in 1993.[64] 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 aSinosauropteryx, a genus related toCompsognathus, shows twooviducts bearing two unlaid eggs. These proportionally larger and less numerous eggs ofSinosauropteryx cast further doubt on the original identification of the purportedCompsognathus eggs.[52] In 1964 German geologistKarl Werner Barthel had explained the discs as gas bubbles formed in the sediment because of the putrefaction of the carcass.[65]
In 2007, William Sellers and Phillip Manning estimated a maximum speed of 17.8 m/s (40 mph) based on a computer model of the skeleton and muscles.[66] This estimate has been criticized by other scholars.[67]
Restoration of anArchaeopteryx chasing a juvenileCompsognathus
During the late Jurassic, Europe was a dry, tropicalarchipelago at the edge of theTethys Sea. The fine limestone in which the skeletons ofCompsognathus have been found originated incalcite from the shells of marine organisms. Both the German and French areas whereCompsognathus specimens have been preserved were lagoons situated between the beaches and coral reefs of the Jurassic European islands in the Tethys Sea.[68] Contemporaries ofCompsognathus longipes include the early avialanArchaeopteryx lithographica and the pterosaursRhamphorhynchus muensteri andPterodactylus antiquus. The same sediments in whichCompsognathus 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 withCompsognathus, indicating that these little dinosaurs might in fact have been the top land predator in these islands.[57]
Much discussion revolved around thetaphonomy of the German specimen, i.e. how the individual died and became fossilized. Reisdorf and Wuttke, in 2012, speculated about the events that lead to the death and transportation of the specimen to its place of burial. First, the individual must have been brought into the lagoon from its habitat, which probably was on the surrounding islands. It is possible that a flash flood swept the animal into the sea, in which case it likely died by drowning. It is also possible that the animal swam or drifted onto the sea, or that it rafted on plants, and was then transported by surface currents to its place of burial. In any case, the specimen would have arrived on the sea floor within a few hours after its death, as otherwise gases forming in its body cavity would have prevented it from sinking in one piece. Water depth at the burial site would have been large enough to prevent refloating of the carcass after such gases were produced. Rounded structures on the slab might have been formed by the release of these gases.[8]
Taphonomic reconstructions are complicated as the exact locality and the position and orientation of the fossil within the sediments is no longer known.[8] As acompression fossil, the specimen would originally have been preserved on both the upper surface of a layer and the lower surface of the subsequent layer (i.e., on a slab and its counter-slab); the counter-slab is now lost. Reisdorf and Wuttke, in 2012, argued that the front and hind limbs of the left side of the body were betterarticulated (still connected together) than those of the right side. This suggests that the specimen is located on the bottom side of the upper slab, and was lying on its left side.[8] The German specimen was preserved with a high degree of articulation—only the skull, hands, cervical ribs and gastralia show disarticulation. The braincase was displaced behind the skull, the first tail vertebra was rotated by 90°, and the tail shows a break between the seventh and eighth tail vertebra.[8]
Illustration of the German specimen
In bothCompsognathus specimens, the neck is strongly curved, with the head coming to rest above the pelvis; the spine of the tail was likewise curved.[69] This posture, known as thedeath pose, is found in many vertebrate fossils, and the GermanCompsognathus specimen was central in several studies that sought to explain this phenomenon. The physician Moodie, in 1918, suggested that the death pose inCompsognathus and similar fossils was the result of anopisthotonus—death throes causing spastic stiffening of the back musculature—while the animal was dying. This hypothesis was soon challenged by paleontologist Friedrich von Huene, who argued that the death pose was the result of desiccation and therefore occurred only after the death. Peter Wellnhofer, in 1991, argued that death poses resulted from the elastic pull of the ligaments, which are released after death.[8] The veterinarian Cynthia Faux and the paleontologist Kevin Padian, in a 2007 study that gained much attention, supported the original opisthotonus hypothesis of Moodie. These authors furthermore argued that upon death, muscles are relaxed and body parts can be easily moved relative to each other. Since opisthotonic postures are already established during death, they may only be preserved if the animal dies in place and becomes buried rapidly. This contradicts previous interpretations on the environment and taphonomy ofCompsognathus and other fossils from the Solnhofen limestones, which assumed very slow burial at the bottom of lagoons into which the carcasses were transported from nearby islands.[8][69] Reisdorf and Wuttke concluded that the death posture indeed resulted from the release of ligaments, more specifically theligamentum elasticum interlaminare, which spans the spine from the neck to tail in modern birds. The release of this ligament would have occurred gradually while the surrounding muscle tissue decayed, and only after the carcass was transported to its final site of deposition.[8]
The bottom water of the lagoon was likely anaerobic (devoid in oxygen), resulting in a sea floor devoid of life except for microbial mats, and therefore preventing scavenging of the carcass.[8] In the trunk region of the German specimen, the surface of the slab is markedly different in texture to the surrounding areas of the slab, showing irregular, nodular surfaces within depressions. Ostrom, in 1978, interpreted these structures as traces of weathering that took place just before the fossil was collected.[5][8] Nopcsa, in 1903, instead suggested that these structures resulted from decomposing tissue of the carcass.[8][61] Reisdorf and Wuttke, in their 2012 study, suggested that the structures are the remains ofadipocere (corpse wax formed by bacteria) that formed around the carcass before burial. Such adipocere would have helped in conserving the state of articulation of the fossil for years when burial was very slow. The presence of adipocere would possibly rule out hypersalinity (very high salt contents) of the bottom water, because such conditions appear to be unfavorable for the adipocere producing bacteria.[8]
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