Temporal range: Early Cretaceous, 124.6–122Ma
|Type specimen with filament impressions, Inner Mongolia Museum|
Ji & Ji, 1996
Ji & Ji, 1996
Sinosauropteryx (meaning "Chinese reptilian wing", Chinese: 中华龙鸟; pinyin: Zhōnghuá lóng niǎo; literally "China dragon bird") is a compsognathid dinosaur. Described in 1996, it was the first dinosaur taxon outside of Avialae (birds and their immediate relatives) to be found with evidence of feathers. It was covered with a coat of very simple filament-like feathers. Structures that indicate colouration have also been preserved for some of the feathers, which makes Sinosauropteryx the first non-avialian dinosaurs where colouration has been determined. Colouration includes a reddish and light banded tail. Some contention has arisen with an alternative interpretation of the filamentous impression as remains of collagen fibres, but this has not been widely accepted.
Sinosauropteryx was a small theropod with an unusually long tail and short arms. The longest known specimen reaches up to 1.07 m (3.5 ft) in length, with an estimated weight of 0.55 kg (1.2 lb). It was a close relative of the similar but older genus Compsognathus, both genera belonging to the family Compsognathidae. Only one species of Sinosauropteryx has been named: S. prima, meaning "first" in reference to its status as the first feathered non-avialian dinosaur species discovered. Three specimens have been described. The third specimen previously assigned to this genus represents either a second, as-yet unnamed species or a distinct, related genus.
Sinosauropteryx lived in what is now northeastern China during the early Cretaceous period. It was among the first dinosaurs discovered from the Yixian Formation in Liaoning Province, and was a member of Jehol Biota. Well-preserved fossils of this species illustrate many aspects of their biology, such as their diet and reproduction.
Sinosauropteryx was a small bipedal theropod, noted for its short arms, large first finger (thumbs), and long tail. The taxon includes some of the smallest known adult non-avian theropod specimens, with the holotype specimen measuring only 68 cm (27 in) in length, including the tail.1 This individual was relatively young.2 The longest known specimen reaches up to 1.07 m (3.5 ft) in length, with an estimated weight of 0.55 kg (1.2 lb).3
Sinosauropteryx was anatomically similar to Compsognathus, differing from its European relatives in its proportions. The skull of Sinosauropteryx was 15% longer than its thigh bones, unlike in Compsognathus, where the skull and thigh bones are approximately equivalent in length. The arms of Sinosauropteryx (humerus and radius) were only 30% the length of its legs (thigh bone and shin), compared to 40% in Compsognathus.1 Additionally, Sinosauropteryx had several features unique among all other theropods. It had 64 vertebrae in its tail. This high number made its tail the longest relative to body length of any theropod.1 Its hands were long compared to its arms, about 84% to 91% of the length of the rest of the arm (humerus and radius), and half the length of the foot. The first and second digits were about the same length, with a large claw on the first digit.2 The first fingers were large, being both longer and thicker than either of the bones of the forearm.1 The teeth differed slightly (they were heterodont) based on position: those near the tips of the upper jaws (on the premaxillae) were slender and lacked serrations, while those behind them (on the maxillae) were serrated and laterally compressed. The teeth of the lower jaws were similarly differentiated.2
A pigmented area in the abdomen of the holotype has been suggested as possible traces of organs,1 and was interpreted as the liver by John Ruben and colleagues, which they described as part of a crocodilian-like "hepatic piston" respiratory system.4 A later study, while agreeing that the pigmented area represented something originally inside the body, found no defined structure and noted that any organs would have been distorted by the processes that flattened the skeleton into an essentially two-dimensional form.2 Dark pigment is also present in the eye region of the holotype and another specimen.1
All described specimens of Sinosauropteryx preserve integumentary structures (filaments arising from the skin) which most palaeontologists interpret as very primitive feathers. These short, down-like filaments are preserved along the back half of the skull, arms, neck, back, and top and bottom of the tail. Additional patches of feathers have been identified on the sides of the body, and palaeontologists Chen, Dong and Zheng proposed that the density of the feathers on the back and the randomness of the patches elsewhere on the body indicated the animals would have been fully feathered in life, with the ventral feathers having been removed by decomposition.1
The filaments are preserved with a gap between the bones, which several authors have noted corresponds closely to the expected amount of skin and muscle tissue that would have been present in life. The feathers are closest to the bone on the skull and end of the tail, where little to no muscle was present, and the gap increases over the back vertebrae, where more musculature would be expected, indicating that the filaments were external to the skin and do not correspond with subcutaneous structures.1
The filaments exhibit random orientations and are often wavy, which has been interpreted as evidence that they were soft and pliable in life. Microscopic examination shows that individual filaments appear dark along the edges and light internally, suggesting that they were hollow, like modern feathers. Compared to modern mammals the filaments were quite coarse, with each individual strand much larger and thicker than the corresponding hairs of similarly sized mammals.1
The length of the filaments varies across the body. On the type specimen, they are shortest just in front of the eyes, with a length of 13 mm (0.51 in). Going further along the body, the filaments rapidly increase in length until reaching lengths of 35 mm (1.4 in) over the shoulder blades. The length remains uniform over the back, until beyond the hips, when the filaments lengthen again and reach their maximum length midway down the tail at 40 mm (1.6 in). The filaments on the underside of the tail are shorter overall and decrease in length more rapidly than those on the dorsal surface. By the 25th tail vertebrae, the filaments on the underside reach a length of only 35 mm (1.4 in). The longest feathers present on the forearm measured 14 mm (0.55 in).1
Though the feathers are too dense to isolate a single structure for examination, several studies have suggested the presence of two distinct filament types (thick and thin) interspersed with each other. The thick filaments tend to appear 'stiffer' than thin filaments, and the thin filaments tend to lie parallel to each other but at angles to nearby thick filaments. These properties suggest that the individual feathers consisted of a central quill (rachis) with thinner barbs branching off from it, similar to but more primitive in structure than modern bird feathers.2 Overall, the filaments most closely resemble the "plumules" or down-like feathers of some modern birds, with a thick central quill and long, thin barbs. The same structures are seen in other fossils from the Yixian Formation, including Confuciusornis.1
While Sinosauropteryx had feather-like structures, it was not very closely related to the previous "first bird" Archaeopteryx.1 There are many dinosaur clades that were more closely related to Archaeopteryx than Sinosauropteryx was, including the deinonychosaurians, the oviraptorosaurians, and the therizinosauroids.5 This indicates that feathers may have been a characteristic of many theropod dinosaurs, not just the obviously bird-like ones, making it possible that equally distant animals such as Compsognathus had feathers as well.5
Sinosauropteryx was the first dinosaur to have its life colouration described by scientists based on physical evidence. Some fossils of Sinosauropteryx show an alternation of lighter and darker bands preserved on the tail. Chen and colleagues initially interpreted this banding pattern as an artifact of the splitting between the main slab and counter-slab in which the original specimen was preserved.1 However, Longrich suggested in his 2002 presentation for the Society of Vertebrate Paleontology that these specimens actually preserve remnants of the colouration pattern the animal would have exhibited in life. He argued that the dark, banded areas on the tail were too evenly spaced to have been caused by random separation of the fossil slabs, and that they represent fossilized pigments present in the feathers. Additionally, rather than an artifact of preservation or decomposition, the presence of dark feathers along only the top of the body may also reflect the colour pattern in life, indicating that Sinosauropteryx prima was countershaded with dark colouration on its back and lighter colouration on its underside, with bands or stripes on the tail for camouflage.6
Longrich's conclusions were supported in a paper first published online in the journal Nature in January 2010. Fucheng Zhang and colleagues examined the fossilized feathers of several dinosaurs and early birds, and found evidence that they preserved melanosomes, the cells that give the feathers of modern birds their colour. Among the specimens studied was a previously undescribed specimen of Sinosauropteryx, IVPP V14202. By examining melanosome structure and distribution, Zhang and colleagues were able to confirm the presence of light and dark bands of colour in the tail feathers of Sinosauropteryx. Furthermore, the team was able to compare melanosome types to those of modern birds to determine a general range of colour. From the presence of phaeomelanosomes, spherical melanosomes that make and store red pigment, they concluded that the darker feathers of Sinosauropteryx were chestnut or reddish brown in colour.7
Despite its feathers, most palaeontologists do not consider Sinosauropteryx to be birds. Phylogenetically, the genus is only distantly related to the clade Aves, usually defined as Archaeopteryx lithographica plus modern birds. The scientists who described Sinosauropteryx, however, used a character-based, or apomorphic, definition of the Class Aves, in which any animal with feathers is considered to be a bird. They argued that the filamentous plumes of Sinosauropteryx represent true feathers with a rachis and barbs, and thus that Sinosauropteryx should be considered a true bird.8 They classified the genus as belonging to a new biological order, Sinosauropterygiformes, family Sinosauropterygidae, within the subclass Sauriurae.9 These proposals have not been accepted, and Sinosauropteryx is generally classified in the family Compsognathidae,1210 a group of small-bodied long-tailed coelurosaurian theropods known from the Late Jurassic and Early Cretaceous of Asia, Europe, and South America.11
Below is a cladogram showing the placement of Sinosauropteryx within Coelurosauria by Senter et al. in 2012.12
There is only one named species of Sinosauropteryx, S. prima. A possible second species is represented by the specimen GMV 2124 (aka NGMC 2124), which was described as a third, larger specimen of S. prima by Ji and Ji in 1997.8 However, in a 2002 presentation and abstract for the Society of Vertebrate Paleontology, Nick Longrich showed that this specimen differs in several anatomical aspects from the others, including its relatively large size, proportionally longer shins, and shorter tail. Longrich suggested that GMV 2124 was a compsognathid coelurosaurian, while Sinosauropteryx proper was a more primitive kind of coelurosaurian or even a basal carnosaurian.6 In 2007, Gishlick and Gauthier concurred that this specimen was probably a new taxon, and tentatively re-classified it as Sinosauropteryx? sp., though they suggested it may belong in a new genus.13 Also in 2007, Ji, Ji and colleagues wrote that GMV 2124 is probably a new genus, noting the differences in tail length and hindlimb proportions.10
Ji and Ji (1996) identified many features that set Sinosauropteryx apart from other birds and dinosaurs. They found that it was a small primitive bird with a relatively high skull, blunt rostrum and a slightly high premaxilla; that the antorbital fenestra was elliptical but not enlarged, the dentary was robust, the surangular was narrow and elongated, and the dentition is extremely well developed and acute; that there are over 50 extremely elongated caudals, constituting 60% of the body length, and the forelimb is extremely short with a short and thick humerus; the pubis was elongated and extremely inflated at its distal end and the ischium is broad; the hind limb was long and robust, the tibia is only slightly longer than the femur, the tarsals are separated, and the metatarsals are relatively robust with unfused proximal ends; the feathers are short, small, and uniform; many ornament the top of the skull, cervical, and dorsal regions, in addition to the dorsal and ventral caudal region.9
The first fossil specimen of the dinosaur later named Sinosauropteryx prima was uncovered in August 1996 by Li Yumin. Yumin was a farmer and part-time fossil hunter who often prospected around Liaoning Province to acquire fossils to sell to individuals and museums. Yumin recognized the unique quality of the specimen, which was separated into two slabs, and sold the slabs to two separate museums in China: the National Geological Museum in Beijing, and the Nanjing Institute of Geology and Paleontology. The director of the Beijing museum, Ji Qiang, recognized the importance of the find, as did visiting Canadian palaeontologist Phil Currie and artist Michael Skrepnick, who became aware of the fossil by chance as they explored the Beijing museum's collections after leading a fossil tour of the area during the first week of October, 1996. Currie recognized the significance of the fossil immediately. As The New York Times quoted him, "When I saw this slab of silt stone mixed with volcanic ash in which the creature is embedded, I was bowled over."14 When originally described, the authors named Sinosauropteryx, meaning "Chinese Reptilian Wing.9
Chinese authorities initially barred photographs of the specimen from publication. However, Currie brought a photograph to the 1996 meeting of the Society of Vertebrate Paleontology at the American Museum of Natural History in New York, causing crowds of palaeontologists to gather and discuss the new discovery. The news reportedly left palaeontologist John Ostrom, who in the 1970s had pioneered the theory that birds evolved from dinosaurs, "in a state of shock."14 Ostrom later joined an international team of researchers who gathered in Beijing to examine the fossils; other team members included feather expert Alan Brush, fossil bird expert Larry Martin, and Peter Wellnhofer, an expert on the early bird Archaeopteryx.15
Three specimens have been assigned to Sinosauropteryx prima: the holotype GMV 2123 (and its counter slab [opposite face], NIGP 127586), NIGP 127587, and D 2141.10 Another specimen, IVPP V14202, was assigned to the genus but not to a species by Zhang and colleagues.7 The assignment of an additional larger specimen to S. prima, GMV 2124, was later found to be in error.1013 All of the fossils were found in the Jianshangou or Dawangzhangzi Beds of the Yixian Formation in the Beipiao and Lingyuan regions of Liaoning, China. These fossil beds have been dated to 124.6–122 million years ago, during the late Barremian to early Aptian stages of the Early Cretaceous.16
Controversy regarding the identity of the filaments preserved in the first Sinosauropteryx specimen began almost immediately, as the team of scientists spent three days in Beijing examining the specimen under a microscope. The results of their studies (reported during a press conference at the Philadelphia Academy of Natural Sciences on Thursday, April 24, 1997) were inconclusive; the team agreed that the structures preserved on Sinosauropteryx were not modern feathers, but suggested further research was required to discover their exact nature.17 Palaeontologist Alan Feduccia, who had not yet examined the specimen, wrote in Audubon Magazine that the structures of Sinosauropteryx (which he considered at the time to be a synonym of Compsognathus, as Compsognathus prima) were stiffening structures from a frill running along the back, and that dinosaur palaeontologists were engaging in wishful thinking when equating the structures with feathers.18 Subsequent publications saw some of the team members disagreeing over the identity of the structures.219
Feduccia's frill argument was followed up in several other publications, in which researchers interpreted the filamentous impressions around Sinosauropteryx fossils as remains of collagen fibres rather than primitive feathers. Since the structures are clearly external to the body, these researchers have proposed that the fibres formed a frill on the back of the animal and underside of its tail, similar to some modern aquatic lizards.20212223 The absence of feathers would refute the proposal that Sinosauropteryx is the most basal known theropod genus with feathers, and also raise questions about the current theory of feather origins itself. It calls into question the idea that the first feathers evolved not for flight but for insulation, and that they made their first appearance in relatively basal dinosaur lineages that later evolved into modern birds.24
Most researchers have disagreed with the identification of the structures as collagen or other structural fibres. Notably, the team of scientists that reported the presence of pigmentation cells in the structures argued that their presence proved the structures were feathers, not collagen, because collagen does not contain pigment.725 Gregory S. Paul reidentified what the collagen hypothesis's proponents consider a body outline outside of the fibres as an artefact of preparation: breakage and brushed-on sealant have been misidentified as the outline of the body.26
The specimen NIGP 127587 was preserved with the remains of a lizard in its gut region, indicating that small, fast-moving animals made up part of the diet of Sinosauropteryx prima. Numerous lizards of this type have been found in the same rocks as Sinosauropteryx, but have yet to be described.1
The possible Sinosauropteryx specimen GMV 2124 (Sinosauropteryx? sp.) was found with three mammal jaws in its gut region. Hurum, Luo, and Kielan-Jaworowska (2006) identified two of these jaws as belonging to Zhangheotherium and the third to Sinobaatar, showing that these two mammals were part of the animal's diet. Zhangheotherium is known to have had a spur on the ankle, like the modern platypus, which would indicate that Sinosauropteryx fed on possibly venomous mammals.27
The same specimen of S. prima which had preserved a lizard in its stomach contents (NIGP 127587) also had several small eggs in its abdomen. Two eggs were preserved just in front of and above the pubic boot, and several more may lie underneath them on the slab. It is unlikely that they were eaten by the animal, as they are in the wrong part of the body cavity for the egg shells to have remained intact. It is more likely that they are unlaid eggs produced by the animal itself. Each egg measured 36 mm (1.4 in) long by 26 mm (1.0 in) wide. The presence of two developed eggs suggests that Sinosauropteryx had dual oviducts and laid eggs in pairs, like other theropods.1
Sinosauropteryx, as a Yixian Formation dinosaur, is a member of the Jehol Biota, the assemblage of organisms found in the Yixian Formation and overlying Jiufotang Formation.16 The Yixian Formation is composed largely of volcanic rocks such as andesite and basalt. Between the volcanic layers are several beds of sedimentary rocks representing deposition in a lake.1 The freshwater lake strata of the Yixian Formation have preserved a wide variety of plants, invertebrates, and vertebrates. Gymnosperm forests were extensive, with a few early flowering plants as well. Ostracods and insects were diverse, and bivalves and gastropods were abundant. Mammals and birds are also well-known from the formation. The setting was subject to periodic mortality events including volcanic eruptions, wildfires, and noxious gases erupting from the lakes.16 The climate has been interpreted as temperate, with distinct wet and dry seasons.28 The yearly temperature during this time period averaged about 10 degrees celsius (50 degrees Fahrenheit), indicating a temperate climate with unusually cold winters for the generally warm Mesozoic era, possibly due to northern China's high latitude during this time.29
- Chen, P.; Dong, Z.; and Zhen, S. (1998). "An exceptionally well-preserved theropod dinosaur from the Yixian Formation of China". Nature 391 (8): 147–152. doi:10.1038/34356.
- Currie, P.J.; and Chen, P.-j. (2001). "Anatomy of Sinosauropteryx prima from Liaoning, northeastern China". Canadian Journal of Earth Sciences 38 (1): 705–727. doi:10.1139/cjes-38-12-1705.
- Therrien, F.; and 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.
- Ruben, J.A.; Jones, T.D.; Geist, N.R.; and Hillenius, W.J. (1997). "Lung structure and ventilation in theropod dinosaurs and early birds". Science 278 (5341): 1267–1270. doi:10.1126/science.278.5341.1267.
- Padian, K. (2004). "Basal Avialae". In Weishampel, David B.; Dodson, Peter; & Osmólska, Halszka (eds.). The Dinosauria (Second ed.). Berkeley: University of California Press. pp. 210–231. ISBN 0-520-24209-2.
- Longrich, N. (2002). "Systematics of Sinosauropteryx". Journal of Vertebrate Paleontology 22 (supplement to 3): 80A.
- Zhang, F.; Kearns, S.L.; Orr, P.J.; Benton, M.J.; Zhou, Z.; Johnson, D.; Xu, X.; and Wang, X. (2010). "Fossilized melanosomes and the colour of Cretaceous dinosaurs and birds". Nature 463 (7284): 1075–1078. doi:10.1038/nature08740. PMID 20107440.
- Ji, Q.; and Ji, S. (1997). "Advances in Sinosauropteryx research". Chinese Geology 7: 30–32.
- Ji, Q.; Ji, S. (1996). "On discovery of the earliest bird fossil in China (Sinosauropteryx gen. nov.) and the origin of birds". Chinese Geology (Beijing: Chinese Geological Museum) 10 (233): 30–33.
- Ji, S.; Gao, C.; Liu, J.; Meng, Q.; and Ji, Q. (2007). "New material of Sinosauropteryx (Theropoda: Compsognathidae) from western Liaoning, China". Acta Geologica Sinica (English Edition) 81 (2): 177–182. doi:10.1111/j.1755-6724.2007.tb00942.x.
- Paul, G. S. (2010). The Princeton Field Guide to Dinosaurs. Princeton, NJ: Princeton University Press. p. 117. ISBN 978-0-691-13720-9.
- Senter, P.; Kirkland, J. I.; Deblieux, D. D.; Madsen, S.; Toth, N. (2012). "New Dromaeosaurids (Dinosauria: Theropoda) from the Lower Cretaceous of Utah, and the Evolution of the Dromaeosaurid Tail". In Dodson, Peter. PLoS ONE 7 (5): e36790. doi:10.1371/journal.pone.0036790. PMC 3352940. PMID 22615813.
- Gishlick, A.D.; and Gauthier, J.A. (2007). "On the manual morphology of Compsognathus longipes and its bearing on the diagnosis of Compsognathidae". Zoological Journal of the Linnean Society 149 (4): 569–581. doi:10.1111/j.1096-3642.2007.00269.x.
- Browne, M.W. (19 October 1996). "Feathery Fossil Hints Dinosaur-Bird Link". New York Times. p. Section 1 page 1 of the New York edition.
- Feduccia, A. (1999). The Origin and Evolution of Birds (Second ed.). Yale University Press. p. 375. ISBN 0-300-07861-7.
- Zhou, Z. (2006). "Evolutionary radiation of the Jehol Biota: chronological and ecological perspectives". Geological Journal 41 (3–4): 377–393. doi:10.1002/gj.1045.
- Stieg, B. (23 April 1997). "Debate rages over birds' relation to dinosaurs". Knight-Ridder Newspapers.
- Morell, V. (1997). "The origin of birds: the dinosaur debate". Audubon Magazine 99 (2): 36–45.
- Martin, L.; and Czerkas, S.A. (2000). "The fossil record of feather evolution in the Mesozoic". American Zoologist 40 (4): 687–694. doi:10.1668/0003-1569(2000)040[0687:TFROFE]2.0.CO;2.
- Geist, N.R.; Jones, T.D.; and Ruben, J.A. (1997). "Implications of soft-tissue preservation in the compsognathid dinosaur, Sinosauropteryx". Journal of Vertebrate Paleontology 7 (supplement to 3): 48A.
- Feduccia, A. (1999). The Origin and Evolution of Birds (2nd ed.). New Haven, Connecticut: Yale University Press. p. 377. ISBN 0-300-07861-7.
- Ruben, J., J. A.; and Jones, T.D. (2000). "Selective factors associated with the origin of fur and feathers". American Zoologist 40 (4): 585–596. doi:10.1093/icb/40.4.585.
- Lingham-Soliar, T.; Feduccia, A.; and Wang, X. (2007). "A new Chinese specimen indicates that 'protofeathers' in the Early Cretaceous theropod dinosaur Sinosauropteryx are degraded collagen fibres". Proceedings of the Royal Society B 274 (1620): 1823–1829. doi:10.1098/rspb.2007.0352. PMC 2270928. PMID 17521978.
- Sanderson, K. (23 May 2007). "Bald dino casts doubt on feather theory". doi:10.1038/news070521-6. Retrieved 14 January 2011.
- Sloan, C. (27 January 2010). "Dinosaur true colors revealed for first time". National Geographic Magazine. Retrieved 14 January 2011.
- Paul, G.S. (2002). Dinosaurs of the air: the evolution and loss of flight in dinosaurs and birds. Baltimore, Maryland: Johns Hopkins University Press. p. 66. ISBN 0-8018-6763-0.
- Hurum, J.H.; Luo, Z.-X.; and Kielan-Jaworowska, Z. (2006). "Were mammals originally venomous?". Acta Palaeontologica Polonica 51 (1): 1–11.
- Wang, Y.; Zheng, S.; Yang, X.; Zhang, W.; and Ni, Q. (2006). "The biodiversity and palaeoclimate of conifer floras from the Early Cretaceous deposits in western Liaoning, northeast China." International Symposium on Cretaceous Major Geological Events and Earth System. p. 56A.
- Amiot, R., Wang, X., Zhou, Z., Xiaolin Wang, X., Buffetaut, E., Lécuyer, C., Ding, Z., Fluteau, F., Hibino, T., Kusuhashi, N., Mo, J., Suteethorn, V., Yuanqing Wang, Y., Xu, X., and Zhang, F. (2011). "Oxygen isotopes of East Asian dinosaurs reveal exceptionally cold Early Cretaceous climates." Proceedings of the National Academy of Sciences, 108(13): 5179-5183. doi: 10.1073/pnas.1011369108
- Sinosauropteryx prima in The Theropod Database