Hesperonychus (meaning "western claw") is a genus of small paravian theropod dinosaur. It may be a dromaeosaurid or an avialan. There is one described species, Hesperonychus elizabethae. The type species was named in honor of Dr. Elizabeth Nicholls of the Royal Tyrrell Museum of Palaeontology who collected it as a student in 1982.[1] It is known from fossils recovered from the Dinosaur Park Formation and possibly from the uppermost strata of the Oldman Formation of Alberta, dating to the Campanian stage of the Late Cretaceous around 75 million years ago.[2]
| Hesperonychus Temporal range: Late Cretaceous,
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|---|---|
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| UALVP 48778, holotype pelvis | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Dinosauria |
| Clade: | Saurischia |
| Clade: | Theropoda |
| Clade: | Pennaraptora |
| Clade: | Paraves |
| Genus: | †Hesperonychus Longrich & Currie, 2009 |
| Species: | †H. elizabethae
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| Binomial name | |
| †Hesperonychus elizabethae Longrich & Currie, 2009
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Description
editHesperonychus is mainly known from one partial pelvic girdle, holotype specimen UALVP 48778, collected by Dr. Elizabeth Nicholls in Dinosaur Provincial Park in 1982. The fossil remained undescribed, however, until Nick Longrich and Phil Currie published on it in 2009. A number of very small toe bones discovered from the Dinosaur Park Formation and Oldman Formation, including "sickle claws", in the collection of the Royal Tyrrell Museum have been tentatively referred to as cf. Hesperonychus.[2]
The gracile appearances of these potential toe bones make it unlikely that Hesperonychus belonged to the Eudromaeosauria. Despite their small size, the pubic bones were fused, a characteristic of adult dinosaurs, indicating that the specimen does not represent a juvenile of a known species.[2] Though known from partial remains, researchers have estimated that it was a small dinosaur measuring about 1 metre (3.3 ft) long and weighing between 1.5 and 2 kilograms (3.3 and 4.4 lb), making it one of the smallest non-avian dinosaurs known from North America.[2][3]
Classification
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A phylogenetic analysis performed by Longrich and Currie found Hesperonychus to be a member of the Microraptorinae,[4] a clade of small dromaeosaurids previously thought to be restricted to the Early Cretaceous of Asia. The authors described this find as "remarkable"; the previously youngest known microraptorine was Microraptor itself from the Aptian stage of the Early Cretaceous, so the discovery of Hesperonychus in the Late Cretaceous Campanian stage pushed the fossil range of microraptorines forward by 45 million years.[2] While the Late Cretaceous, North American Bambiraptor had sometimes been classified as a microraptorine, other researchers (including Longrich and Currie) have found that it is more closely related to Saurornitholestes.[2]
Hesperonychus was assigned to Microraptoria due to having a spatulate (rounded) pubic symphysis, a strong posterior curvature of the distal shaft of the pubis, and lateral tubercules on the pubes, which are expanded into 'wing-like' structures in the case of Hesperonychus.[2]
Cladogram (2012):[5]
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However, subsequent studies have questioned its identity as a microraptorine, with some researchers excluding the taxon from phylogenetic analyses due to its fragmentary remains and others classifying it in various positions within or outside dromaeosaurids. In 2012, Martyniuk considered Hesperonychus as a eudromaeosaurian.[6] In 2013, microraptorines were considered as averaptorans outside dromaeosaurids.[7] In 2014, Brusatte and colleagues pruned five "wildcard" taxa including the paravians Pyroraptor and Hesperonychus from phylogenetic analyses, mainly due to a huge lack of data, indicating that the definitive classifications of these taxa are uncertain.[8] Other studies have also followed this exclusion of Hesperonychus.[9][10][11][12]
In 2019, Hartman and colleagues suggested that Hesperonychus is actually an avialan close to modern birds like Balaur bondoc based on phylogenetic analyses, though they disagreed with microraptorines being avialans.[13] In the same year, Rauhut and colleagues considered various genera of theropods including Hesperonychus as 'problematic taxa' due to their unstable phylogenetic position.[14] In 2020, Hesperonychus was recovered as a dromaeosaurid and a sister taxon, but not a member, of the polytomic microraptorines.[15]
Paleobiology
editMicroraptorines are well known for their small size and, in some cases, ability to fly or glide. Longrich and Currie concluded that it was unlikely for Hesperonychus to exhibit four wings or gliding behavior as in Microraptor, and speculated that it was more likely to be similar to Sinornithosaurus given their closer similarity in size. Nevertheless, Hesperonychus seems to show that microraptorines did not vary much in size, remaining very small relative to other dromaeosaurids throughout their history,[2] though it is questionable whether it was indeed a microraptorine or a dromaeosaurid.[13]
Whether it was a microraptorine or not, the discovery of Hesperonychus filled in a gap in the ecology of Late Cretaceous North America. Unlike roughly contemporary environments in Europe and Asia, North America appeared to lack very small carnivorous dinosaurs. In modern ecosystems dominated by endothermic mammals, small animal species outnumber larger ones. Since dinosaurs are also presumed to have been endotherms, the lack of small species and great number of known large species in North America was unusual.[2] Hesperonychus helped to fill that gap, especially since, given the number of fragmentary remains and claws that have been collected (representing at least ten distinct specimens, compared to thirty of the contemporary Saurornitholestes and two of Dromaeosaurus), it appears to have been a very common feature of the Dinosaur Park Formation environment.[2]
The next smallest carnivore in the environment was the mammal Eodelphis, which weighed only 600 grams. There does not appear to have been any overlap between the smallest dinosaurs and the largest mammals in ecosystems such as this, which Longrich and Currie explained by hypothesizing that either competition from dinosaurs kept mammals from growing larger (the traditional view), competition from mammals kept the dinosaurs from growing smaller, or both.[2]
See also
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References
edit- ^ Alberta researchers discover mini meat-eating dinosaur, a 16 March 2009 article from CBC News
- ^ a b c d e f g h i j k Longrich, N.R.; Currie, P.J. (2009). "A microraptorine (Dinosauria–Dromaeosauridae) from the Late Cretaceous of North America". Proceedings of the National Academy of Sciences. 106 (13): 5002–5007. Bibcode:2009PNAS..106.5002L. doi:10.1073/pnas.0811664106. PMC 2664043. PMID 19289829.
- ^ Paul, Gregory S. (2016). The Princeton Field Guide to Dinosaurs. Princeton University Press. p. 150. ISBN 978-1-78684-190-2. OCLC 985402380.
- ^ Canadian dig yields tiny dinosaur, a 16 March 2009 article from BBC News
- ^ 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 3352940. PMID 22615813.
- ^ Martyniuk, Matthew P. (2012). "Restoring Mesozoic Birds". A Field Guide to Mesozoic Birds and Other Winged Dinosaurs. Pan Aves. pp. 32–52. ISBN 978-0988596504.
- ^ Agnolín, Federico L.; Novas, Fernando E. (2013), "Discussion", Avian Ancestors, Dordrecht: Springer Netherlands, pp. 49–57, doi:10.1007/978-94-007-5637-3_5, ISBN 978-94-007-5636-6, retrieved 20 June 2024
- ^ Brusatte, Stephen L.; Lloyd, Graeme T.; Wang, Steve C.; Norell, Mark A. (2014). "Gradual Assembly of Avian Body Plan Culminated in Rapid Rates of Evolution across the Dinosaur-Bird Transition" (PDF). Current Biology. 24 (20): 2386–2392. doi:10.1016/j.cub.2014.08.034. PMID 25264248. S2CID 8879023. Supplementary Information
- ^ Lü, Junchang; Brusatte, Stephen L. (2015). "A large, short-armed, winged dromaeosaurid (Dinosauria: Theropoda) from the Early Cretaceous of China and its implications for feather evolution". Scientific Reports. 5: Article number 11775. doi:10.1038/srep11775. PMC 4504142. PMID 26181289.
- ^ Cau, Andrea; Brougham, Tom; Naish, Darren (2015). "The phylogenetic affinities of the bizarre Late Cretaceous Romanian theropod Balaur bondoc (Dinosauria, Maniraptora): Dromaeosaurid or flightless bird?". PeerJ. 3: e1032. doi:10.7717/peerj.1032. PMC 4476167. PMID 26157616.
- ^ Brownstein, C.D. (2019). "Halszkaraptor escuilliei and the evolution of the paravian bauplan". Nature. 9 (1): 16455. Bibcode:2019NatSR...916455B. doi:10.1038/s41598-019-52867-2. PMC 6848195. PMID 31712644.
- ^ Brownstein, C.D. (2021). "Dromaeosaurid crania demonstrate the progressive loss of facial pneumaticity in coelurosaurian dinosaurs". Zoological Journal of the Linnean Society. 191 (1): 87–112. doi:10.1093/zoolinnean/zlaa048.
- ^ a b Hartman, Scott; Mortimer, Mickey; Wahl, William R.; Lomax, Dean R.; Lippincott, Jessica; Lovelace, David M. (10 July 2019). "A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flight". PeerJ. 7: e7247. doi:10.7717/peerj.7247. ISSN 2167-8359. PMC 6626525. PMID 31333906.
- ^ Rauhut, Oliver WM; Tischlinger, Helmut; Foth, Christian (14 May 2019). "A non-archaeopterygid avialan theropod from the Late Jurassic of southern Germany". eLife. 8: e43789. doi:10.7554/eLife.43789. ISSN 2050-084X. PMC 6516837. PMID 31084702.
- ^ Jasinski, Steven E.; Sullivan, Robert M.; Dodson, Peter (December 2020). "New Dromaeosaurid Dinosaur (Theropoda, Dromaeosauridae) from New Mexico and Biodiversity of Dromaeosaurids at the end of the Cretaceous". Scientific Reports. 10 (1): 5105. Bibcode:2020NatSR..10.5105J. doi:10.1038/s41598-020-61480-7. PMC 7099077. PMID 32218481.