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{{Automatic taxobox
{{speciesbox
| fossil_range = [[Early Cretaceous]], {{fossil range|124.6}}
| fossil_range = [[Early Cretaceous]], <br>~{{fossil range|125}}
| image = Beipiaosaurus skeletal Headden.jpg
| image = Beipiaosaurus holotype fossil.png
| image_caption = Components of the holotype specimen (prior to the caudal vertebrae re-excavation)
| image_caption = Skeletal diagram
| image_upright = 1.1
| display_parents = 2
| display_parents = 2
| genus = Beipiaosaurus
| taxon = Beipiaosaurus
| parent_authority = [[Xu Xing (paleontologist)|Xu]], [[Tang Zhilu|Tang]] & [[Wang Xiaolin|Wang]], 1999
| authority = [[Xu Xing (paleontologist)|Xu]] et al. [[1999 in paleontology|1999]]
| species = inexpectus
| type_species = {{extinct}}'''''Beipiaosaurus inexpectus'''''
| authority = Xu, Tang & Wang, 1999
| type_species_authority = Xu et al. 1999
}}
}}


'''''Beipiaosaurus''''' {{IPAc-en|ˌ|b|eɪ|p|j|aʊ|ˈ|s|ɔː|r|ə|s}} is a [[genus]] of [[Therizinosauroidea|therizinosauroid]] [[theropod]] [[dinosaur]] from the [[Early Cretaceous]] of [[China]]. Before the discovery of ''[[Yutyrannus]]'', it was among the largest dinosaurs known from direct evidence to be feathered.
'''''Beipiaosaurus''''' {{IPAc-en|ˌ|b|eɪ|p|j|aʊ|ˈ|s|ɔː|r|ə|s}} is a [[genus]] of [[Therizinosauroidea|therizinosauroid]] [[theropod]] [[dinosaurs]] that lived in [[Asia]] during the [[Early Cretaceous]] in the [[Yixian Formation]]. The first remains were found in 1996 and formally described in 1999. Before the discovery of ''[[Yutyrannus]]'', they were among the largest dinosaurs known from direct evidence to be feathered. ''Beipiaosaurus'' is known from three reported specimens preserving numerous impressions of feather structures that allowed to determine the feathering color which turned out to be brownish.

They were relatively small-sized therizinosaurs, measuring {{convert|2.2|m|ft|abbr=on}} long and weighing about {{convert|45|-|91|kg|lb|abbr=on}} in contrast to the advanced and giant ''[[Segnosaurus]]'' or ''[[Therizinosaurus]]''. The necks of ''Beipiaosaurus'' were shorter than in most therizinosaurs, whose are characterized by elongated necks adapted for [[Browsing (herbivory)|high-browsing]]. Also, their feet configuration differs from therizinosaurids, having a generic three-toed pes instead of four as seen in other members.


The exact classification of therizinosaurs had in the past been hotly debated, since their [[prosauropod]]-like teeth and body structure indicate that they were generally herbivorous, unlike typical theropods. ''Beipiaosaurus'', being considered to be a primitive therizinosauroid, has features which suggest that all therizinosauroids, including the more derived [[Therizinosauridae]], to be [[coelurosauria]]n theropods, not [[sauropodomorph]] or [[ornithischian]] relatives as once believed.
The exact classification of therizinosaurs had in the past been hotly debated, since their [[prosauropod]]-like teeth and body structure indicate that they were generally herbivorous, unlike typical theropods. ''Beipiaosaurus'', being considered to be a primitive therizinosauroid, has features which suggest that all therizinosauroids, including the more derived [[Therizinosauridae]], to be [[coelurosauria]]n theropods, not [[sauropodomorph]] or [[ornithischian]] relatives as once believed.


==History of discovery==
==Discovery==
In 1996, the peasant Li Yinxian discovered a skeleton of a theropod dinosaur near the village of [[Sihetun]]. In the May 27, 1999, issue of the journal ''[[Nature (journal)|Nature]]'' the discovery was announced and the [[type species]] ''Beipiaosaurus inexpectus'' named and described by [[Xu Xing (paleontologist)|Xu Xing]], [[Tang Zhilu]] and [[Wang Xiaolin]]. The generic name ''Beipiaosaurus'' translates as "Beipiao lizard" after [[Beipiao]], a city in [[China]] near the location of its discovery. ''Beipiaosaurus'' is known from a single species, ''B. inexpectus'', the [[specific name (zoology)|specific name]], meaning "unexpected" in [[Latin]], referring to "the surprising features in this animal".<ref name="xu99">{{cite journal | last1 = Xu | first1 = X. | last2 = Tang | first2 = Z-L. | last3 = Wang | first3 = X-L. | year = 1999 | title = A therizinosauroid dinosaur with integumentary structures from China | doi = 10.1038/20670 | journal = Nature | volume = 399 | issue = 6734| pages = 350–354 }}</ref>
In 1996, the peasant Li Yinxian discovered a skeleton of a theropod dinosaur near the village of [[Sihetun]]. In the May 27, 1999, issue of the journal ''[[Nature (journal)|Nature]]'' the discovery was announced and the [[type species]] ''Beipiaosaurus inexpectus'' named and described by [[Xu Xing (paleontologist)|Xu Xing]], [[Tang Zhilu]] and [[Wang Xiaolin]]. The generic name ''Beipiaosaurus'' translates as "Beipiao lizard" after [[Beipiao]], a city in [[China]] near the location of its discovery. ''Beipiaosaurus'' is known from a single species, ''B. inexpectus'', the [[specific name (zoology)|specific name]], meaning "unexpected" in [[Latin]], referring to the"surprising features in these animals".<ref name="xu99">{{cite journal|last1=Xu|first1=X.|last2=Tang|first2=Z.-L.|last3=Wang|first3=X. L.|date=1999|title=A therizinosauroid dinosaur with integumentary structures from China|journal=Nature|volume=339|issue=6734|pages=350–354|bibcode=1999Natur.399..350X|doi=10.1038/20670|issn=14764687}}</ref>
[[File:Beipiaosaurus holotype fossil.png|left|thumb|241x241px|Components of the holotype fossil]]
[[File:Beipiaosaurus skeletal Headden.jpg|left|thumb|Skeletal composite of IVPP V11559 and STM 31-1]]
The [[holotype]] ([[Type (biology)|type specimen]]) of ''Beipiaosaurus inexpectus'', [[holotype]] IVPP V11559, was recovered in the Jianshangou Beds of the [[Yixian Formation]] in [[Liaoning]] Province, [[China]]. The specimen was collected in sediment deposited during the [[Aptian]] [[faunal stage|stage]] of the [[Cretaceous]] period, approximately 125 to 124 million years ago.<ref name="zhou2006">{{cite journal | last1 = Zhou | first1 = Z | year = 2006 | title = Evolutionary radiation of the Jehol Biota: chronological and ecological perspectives | url = | journal = Geological Journal | volume = 41 | issue = | pages = 377–393 | doi=10.1002/gj.1045}}</ref> This specimen is housed in the collection of the [[Institute of Vertebrate Paleontology and Paleoanthropology]], in [[Beijing]], China. It consists of a partial, sub-adult, skeleton that is largely disarticulated. A significant number of fossilized bones were recovered, including: cranial fragments, a [[mandible]], teeth, three cervical [[vertebrae]], four dorsal vertebrae, four dorsal ribs, two sacral vertebrae, twenty-five caudal vertebrae, a pygostyle, three chevrons, an incomplete furcula and [[scapula]], two coracoids, a complete forelimb, a partial forelimb, both ilia, an incomplete pubis, an incomplete ischium, a femur, both tibiae (one incomplete), an incomplete fibula, an astragalus, a calcaneum, several tarsals, metatarsals, and unguals, and remains of the [[integument]], including feathers.
The [[holotype]] ([[Type (biology)|type specimen]]) of ''Beipiaosaurus inexpectus'', '''IVPP V11559''', was recovered in the Jianshangou Beds of the [[Yixian Formation]] in [[Liaoning]] Province, [[China]]. The specimen was collected in sediment deposited during the [[Aptian]] [[faunal stage|stage]] of the [[Early Cretaceous]] period, approximately 125 million years ago.<ref name="zhou2006">{{cite journal|last1=Zhou|first1=Z.|date=2006|title=Evolutionary radiation of the Jehol Biota: chronological and ecological perspectives|journal=Geological Journal|volume=41|issue=3-4|pages=377–393|doi=10.1002/gj.1045|doi-access=free}}</ref> It is housed in the collection of the [[Institute of Vertebrate Paleontology and Paleoanthropology]], in [[Beijing]], China. It consists of a partial, sub-adult, skeleton that is largely disarticulated. A significant number of fossilized bones were recovered, including: cranial fragments, a [[mandible]], [[teeth]], three [[cervical vertebrae]], four [[dorsal vertebrae]], four dorsal [[ribs]], two [[Glossary of dinosaur anatomy#sacrals|sacral vertebrae]], twenty-five [[Glossary of dinosaur anatomy#caudals|caudal vertebrae]] with a [[pygostyle]], three [[Chevron (anatomy)|chevrons]], an incomplete [[furcula]] and [[scapula]], both [[coracoids]], both forelimbs, both [[Ilium (bone)|ilia]], an incomplete [[Pubis (bone)|pubis]], an incomplete [[ischium]], a [[femur]], both [[tibiae]] (one incomplete), an incomplete [[fibula]], the [[Glossary of dinosaur anatomy#astragalus|astragalus]] and [[Glossary of dinosaur anatomy#calcaneum|calcaneum]], several [[Glossary of dinosaur anatomy#tarsals|tarsals]], [[metatarsals]], manual and pedal [[unguals]], and skin impressions of the primitive plumage.<ref name="xu99"/><ref name=Xu2003>{{cite journal|last1=Xu|first1=X.|last2=Cheng|first2=Y.|last3=Wang|first3=X.-L.|last4=Chang|first4=C.|date=2003|title=Pygostyle‐like Structure from Beipiaosaurus (Theropoda, Therizinosauroidea) from the Lower Cretaceous Yixian Formation of Liaoning, China|journal=Acta Geologica Sinica|volume=77|issue=3|pages=294–298|doi=10.1111/j.1755-6724.2003.tb00744.x|url=https://www.researchgate.net/publication/227941209}}</ref> The pelvic girdle and caudal vertebrae were discovered during a re-excavation of the fossil quarry were the first elements of the holotype were found. These rediscovered elements helped to complete the holotype specimen.<ref name=Xu2003/>


A second specimen, STM 31-1, a partial skeleton, was described by Xu ''et al.'' in 2009, which preserved a significant covering of unique, elongated feathers. This specimen consisted of a complete skull, a sclerotic ring, the mandible, the atlas and axis bones, nine additional cervical vertebrae, dorsal vertebrae, seventeen cervical ribs, twelve dorsal ribs, both scapulae and coracoids, one complete humerus and proximal humerus, one complete radius and distal radius, one complete ulna and distal ulna, carpals, and some metacarpals.<ref name="xu2009">{{cite journal | last1 = Xu | first1 = X. | last2 = Zheng | first2 = | last3 = You | first3 = | year = 2009 | title = A new feather type in a nonavian theropod and the early evolution of feathers | url = | journal = Proceedings of the National Academy of Sciences | volume = 106 | issue = 3| pages = 832–834 | doi = 10.1073/pnas.0810055106 | pmid=19139401 | pmc=2630069}}</ref> The rear of the skull of this specimen was badly crushed.
A second specimen, '''STM 31-1''', a partial skeleton, was described by Xu et al. 2009, which preserves a significant covering of unique, elongated feathers. This specimen consisted of a complete skull, a sclerotic ring, the mandible, the atlas and axis bones, nine additional cervical vertebrae, dorsal vertebrae, seventeen cervical ribs, twelve dorsal ribs, both scapulae and coracoids, one complete humerus and proximal humerus, one complete radius and distal radius, one complete ulna and distal ulna, carpals, and some metacarpals. The rear of the skull of this specimen was badly crushed.<ref name="xu2009">{{cite journal|last1=Xu|first1=X.|last2=Zheng|first2=X.|last3=You|first3=H.|date=2009|title=A new feather type in a nonavian theropod and the early evolution of feathers|journal=Proceedings of the National Academy of Sciences|volume=106|issue=3|pages=832–834|doi=10.1073/pnas.0810055106|doi-access=free|pmc=2630069|pmid=19139401}}</ref> Li et al. 2014 mentioned a third specimen labelled under the number '''BMNHC PH000911'''. This specimen hails from the Sihetun locality at the Beipiao County in Liaoning Province and compromises a partial individual preserving the skull (badly crushed), most of the vertebral colum, both arms and other postcrania. Traces of feather integument were found around the neck area.<ref name=Li2014>{{cite journal|last1=Li|first1=Q.|last2=Clarke|first2=J. A.|last3=Gao|first3=K.-Q.|last4=Zhou|first4=C.-F.|last5=Meng|first5=Q.|last6=Li|first6=D.|last7=D’Alba|first7=L.|last8=Shawkey|first8=M. D.|date=2014|title=Melanosome evolution indicates a key physiological shift within feathered dinosaurs|journal=Nature|volume=507|issue=7492|pages=350–353|doi=10.1038/nature12973|pmid=24522537|url=https://www.academia.edu/6860358}}</ref>


==Description==
==Description==
[[File:Beipiaosaurus size.png|thumb|Size comparison between an average individual and a 1.8 m tall human]]
[[File:Beipiao1mmartyniuk.png|thumb|Restoration]]
''Beipiaosaurus'' were small-sized therizinosaurs, measuring {{convert|2.2|m|ft|abbr=on}} in length, and before the discovery of ''[[Yutyrannus]]'' they were among the largest dinosaurs known from direct evidence to be feathered.<ref name="xu99"/> They are estimated to have weigh between {{convert|45|to|91|kg|lb|abbr=on}}.<ref name=Holtz2012>{{cite book|last1=Holtz|first1=T. R.|year=2007|title=Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages|last2=Rey|first2=L. V.|date=2007|publisher=Random House|isbn=9780375824197}} [https://www.geol.umd.edu/~tholtz/dinoappendix/HoltzappendixWinter2011.pdf Genus List for Holtz 2012] [https://www.geol.umd.edu/~tholtz/dinoappendix/appendix.html Weight Information]</ref> More advanced therizinosaurids have four functional [[toes]], but the feet of ''Beipiaosaurus'' still have reduced inner toes, showing that the derived therizinosaurid condition may have evolved from a three-toed therizinosauroid ancestor. The head was large relative to other therizinosaurs, with the lower jaw measuring about same length as the [[femur]]. The neck appears to be shorter compared to other therizinosaurs.<ref name="xu99"/><ref name="xu2009"/> In 2003 the [[pygostyle]], consisting of the fused five last vertebrae of the tail, was described in greater detail, suggesting that the original function of the pygostyle was not linked with pennaceous feathers.<ref name=Xu2003/>
''Beipiaosaurus'' measured 2.2 meters (7.3&nbsp;ft) in length, and before the discovery of ''[[Yutyrannus]]'' is among the largest dinosaurs known from direct evidence to be feathered.<ref name="xu99"/>


===Distinguishing traits===
More advanced therizinosaurids have four functional toes, but the feet of ''Beipiaosaurus'' still have reduced inner toes, showing that the derived therizinosaurid condition may have evolved from a three-toed therizinosauroid ancestor.
According to Zanno in 2010, ''Beipiaosaurus'' can be distinguished from other therizinosaur taxa based on the following characteristics, which are unique derived traits ([[autapomorphies]]): a low ridge is present on the front of the thighbone shaft which extends upwards from the inner condyle; the last four dorsal vertebrae are fused; from at least the seventh vertebra onwards the tail vertebrae are fused into a pygostyle; a prominent triangular flange extends outwards, away from the body, from the underside of the first [[metacarpal]]; the skull is large, about as long as the thighbone; the first phalanx of the first digit has a joint surface with the claw, that is elongated in the direction of the finger tip on the outer side of its lower part; on the front edge of the [[ischium]] a projection, the obturator process, has a wavy profile with a tip that is curved downwards; the "boot" at the lower end of the ischium has twice the width, measured from the front to the rear, of the lower shaft of the ischium.<ref name=Zanno2010/>
The head was large relative to other therizinosaurs, with the lower jaw measuring about same length as the femur.<ref name="xu99"/> In 2003 the pygostyle, consisting of the fused five last vertebrae of the tail, was described in greater detail.<ref name=Xu2003>{{cite journal |author=Xu, X. |author2=Cheng, Y. |author3=Wang, X-L. |author4=Chang C. |year=2003 |title=Pygostyle-like structure from ''Beipiaosaurus'' (Theropoda, Therizinosauroidea) from the Lower Cretaceous Yixian Formation of Liaoning, China |journal=Acta Geologica Sinica|publisher= |volume=77 |issue=3 |pages=294–298 |url= |doi= 10.1111/j.1755-6724.2003.tb00744.x|pmid= |pmc= }}</ref>


In 2019 Liao and Xu redescribed the holotype skull in detail, noting new unique cranial traits for ''Beipiaosaurus''. These consisted of the large postorbital joint of the frontal and its abrupt transition from the orbital edge, a long and keen anterior joint of the parietal, an elongate bottom branching of the squamosal articulation of the parietal, and the deeply external mandibular fenestra that is located towards the rear.<ref>{{cite journal|last1=Liao|first1=C.-C.|last2=Xu|first2=X.|date=2019|title=Cranial osteology of Beipiaosaurus inexpectus (Theropoda: Therizinosauria)|journal=Vertebrata PalAsiatica|volume=57|issue=2|pages=117–132|doi=10.19615/j.cnki.1000-3118.190115|url=https://www.researchgate.net/publication/332368922}}</ref>
===Distinguishing anatomical features===
A diagnosis is a statement of the anatomical features of an organism (or group) that collectively distinguish it from all other organisms. Some, but not all, of the features in a diagnosis are also autapomorphies. An autapomorphy is a distinctive anatomical feature that is unique to a given organism.


===Feathers and color===
According to Zanno (2010b), ''Beipiaosaurus'' can be distinguished from its direct relatives based on the following characteristics, which are its unique derived traits, or [[autapomorphies]]:<ref name=zanno10/>
[[File:Beipiaosaurus-Paleozoological Museum of China.jpg|alt=|left|thumb|Feather impressions on the left arm from the holotype on display at the [[Paleozoological Museum of China]]]]
The first feather impressions were found in the holotype specimen, consisting of short, slender filamentous feathers on the left arm. These impressions indicated that the body was predominately covered by downy feather-like fibers, similar to those of ''[[Sinosauropteryx]]'', but longer, and oriented perpendicular to the arm. Xu et al. 1999 suggested that these downy feathers represent an intermediate stage between ''Sinosauropteryx'' and more advanced birds ([[Avialae]]).<ref name="xu99"/> The tail was also covered in feathers between four and seven centimeters long, consisting of parallel filaments with a width of {{convert|1.5|mm|cm|abbr=on}}, without a trace of [[pennaceous feather]]s or a tail fan, as indicated by the preserved [[pygostyle]].<ref name="Xu2003"/>


Unique among known theropods, ''Beipiaosaurus'' also possessed a secondary coat of much longer, simpler feathers that rose out of the down layer. These unique feathers known as EBFFs (elongated broad filamentous feathers) were first described by Xu et al. 2009, based on specimen STM 31-1 consisting of the torso, head and neck. Xu and his team also found EBFFs in the tail of the holotype IVPP V11559, which were revealed by further preparation. Some of these were damaged during preparation though.<ref name="xu2009"/>
* A low ridge is present on the front of the thighbone shaft which extends upwards from the inner condyle (according to Zanno, 2008)
[[File:Feather stages diagram.svg|thumb|Diagram illustrating feather evolution stages. ''Beipiaosaurus'' falls within stage 1 and stage 2]]
* The last four dorsal vertebrae are fused (according to Zanno, 2008)
The EBFFs differ from other feather types in that they consist of a single, unbranched filament. Most other primitive [[feathered dinosaurs]] have down-like feathers made up of two or more filaments branching out from a common base or along a central shaft. The EBFFs of ''Beipiaosaurus'' are also much longer than other primitive feather types, measuring about {{convert|100|-|150|mm|cm|abbr=on}} long, roughly half the length of the neck. In ''Sinosauropteryx'', the longest feathers are only about 15% of the neck length. The EBFFs of ''Beipiaosaurus'' are also unusually broad, up to {{convert|3|mm|cm|abbr=on}} wide in the holotype. The broadest feathers of ''Sinosauropteryx'' are only {{convert|0.2|mm|cm|abbr=on}} wide, and only slightly wider in larger forms such as ''[[Dilong (dinosaur)|Dilong]]''. Additionally, where most primitive feather types are circular in cross section, EBFFs appear to be oval-shaped. None of the preserved EBFFs were curved or bent beyond a broad arc in either specimen, indicating that they were fairly stiff. They were probably hollow, at least at the base.<ref name="xu2009"/>
* From at least the seventh vertebra onwards the tail vertebrae are fused into a [[pygostyle]]
* A prominent triangular flange extends outwards, away from the body, from the underside of the first [[metacarpal]] (according to Zanno, 2008)
* The skull is large, about as long as the thighbone (according to Xu et al., 1999)
* The first phalanx of the first digit has a joint surface with the claw, that is elongated in the direction of the finger tip on the outer side of its lower part (according to Xu et al., 1999)
* On the front edge of the [[ischium]] a projection, the obturator process, has a wavy profile with a tip that is curved downwards (according to Zanno, 2008)
* The "boot" at the lower end of the ischium has twice the width, measured from the front to the rear, of the lower shaft of the ischium (according to Zanno, 2008)


In 2009 during a interview at [[Live Science]], Xu stated: "Both are definitely not for flight, inferring the function of some structures of extinct animals would be very difficult, and in this case, we are not quite sure whether these feathers are for display or some other functions." He speculated that the finer feathers served as an insulatory coat and that the larger feathers were ornamental, perhaps for social interactions such as mating or communication.<ref>{{cite news|last1=Bryner|first1=J.|date=2009-01-15|title=Ancient Dinosaur Wore Primitive Down Coat|url=http://www.foxnews.com/story/0,2933,479875,00.html|url-status=dead|work=Fox News|location=New York|archive-url=https://web.archive.org/web/20090304193859/http://www.foxnews.com/story/0,2933,479875,00.html|archive-date=2009-03-04}}</ref>
===Feathers===
[[File:Beipiaosaurus-Paleozoological Museum of China.jpg|alt=|left|thumb|Preserved feathers from the holotype on display at the [[Paleozoological Museum of China]].]]
[[File:Beipiaosaurus Restoration.png|thumb|left|[[Paleoart|Life restoration]]]]
Li et al. 2014 compared the color and shape of the melanosomes in 181 extant animal specimens, 13 fossil specimens (including ''Beipiaosaurus'') and previous data about the melanosome diversity using [[scanning electron microscopes]]. They found that color in dinosaurs seem to be slightly connected with their physiology. While some species of living reptiles (lizards or crocodiles, which are [[ectothermic]]) have less diversity in the shape of melanosomes and darker color ranges, some maniraptorans, birds and mammals (which are [[endothermic]]) have an increased diversity of melanosome shapes and more vivid colors. The examined specimen of ''Beipaosaurus'', BMNHC PH000911, preserves feather impressions which are located in the neck area. These are filamentous/sparce in structure and the sampled melanosomes were sphere-shaped and inferred to had a brownish colouration like those in modern reptiles which fall within the range of dark brownish colourations.<ref name=Li2014/>
Soft-tissue impressions from the type specimen of ''B. inexpectus'' indicated that the body was covered predominately by downy feather-like fibers, similar to those of ''[[Sinosauropteryx]]'', but longer, and oriented perpendicular to the arm. Xu ''et al.'', who described the specimen, suggested that these downy feathers represent an intermediate stage between ''Sinosauropteryx'' and more advanced birds ([[Avialae]]).<ref name="xu99" /> The tail was covered in feathers between four and seven centimeters long, consisting of parallel filaments with a width of 1.5 millimeters, without a trace of [[pennaceous feather]]s or a tail fan.<ref name="Xu2003" />


''[[Jianchangosaurus]]'' is another primitive therizinosaur taxon known from the same formation that was found with impressions of a series of filamentous and unbranched feathers in its holotype specimen. Only the distal ends of the feather impressions are visible and based on their morphology the feathers are considered to be EBFFs, bearing resemblance to those found along the specimens of ''Beipiaosaurus''. These findings suggest that they might have been used for visual display and were common among early therizinosaurs.<ref name=Pu2013>{{cite journal|last1=Pu|first1=H.|last2=Kobayashi|first2=Y.|last3=Lü|first3=J.|last4=Xu|first4=L.|last5=Wu|first5=Y.|last6=Chang|first6=H.|last7=Zhang|first7=J.|last8=Jia|first8=S.|date=2013|title=An Unusual Basal Therizinosaur Dinosaur with an Ornithischian Dental Arrangement from Northeastern China|journal=PLoS ONE|volume=8|issue=5|pages=e63423|doi=10.1371/journal.pone.0063423|doi-access=free|pmc=3667168|pmid=23734177}}</ref>
Unique among known theropods, ''Beipiaosaurus'' also possessed a secondary coat of much longer, simpler feathers that rose out of the down layer.<ref name="Bryner09">Bryner, Jeanna (2009). "Ancient Dinosaur Wore Primitive Down Coat." http://www.foxnews.com/story/0,2933,479875,00.html {{Webarchive|url=https://web.archive.org/web/20090304193859/http://www.foxnews.com/story/0,2933,479875,00.html |date=2009-03-04 }}</ref> These unique feathers (known as EBFFs, or elongated broad filamentous feathers) were first described by Xu ''et al.'' in 2009, based on a specimen consisting of the torso, head and neck. Xu and his team also found EBFFs in the original type specimen of ''B. inexpectus'', revealed by further preparation.


==Classification==
The EBFFs differ from other feather types in that they consist of a single, unbranched filament. Most other primitive [[feathered dinosaurs]] have down-like feathers made up of two or more filaments branching out from a common base or along a central shaft. The EBFFs of ''Beipiaosaurus'' are also much longer than other primitive feather types, measuring about 100-150 millimeters (4-6&nbsp;inches) long, roughly half the length of the neck. In ''Sinosauropteryx'', the longest feathers are only about 15% of the neck length.
[[File:Therizinosauroids illium comparison.png|thumb|Schematic comparison of the ilium of ''Beipiaosaurus'' (in B) and other related therizinosaurs]]
The affinities of therizinosaurs were originally obscure and often problematic, giving rise to taxonomic debate since they feature similar adaptations to the unrelated [[sauropodomorphs]] and [[ornithischians]]. The description of ''Beipiaosaurus'' helped to assemble the definitive placement of therizinosaurs within the [[Theropoda]], especially as [[maniraptora]]ns thanks to the numerous theropod features and irrefutable feather impressions in the holotype.<ref name="xu99"/>


''Beipiaosaurus'' was first assigned to the [[Therizinosauroidea]], in a very primitive position by Xu et al. 1999.<ref name="xu99"/> All subsequent [[phylogenetic]] analyses have confirmed this assignment. According to the definition by [[Paul Sereno]] of this group, ''Beipiaosaurus'' is even by definition the basal most member. [[Lindsay E. Zanno]] noted that ''Beipiaosaurus'' shares a sister-taxon relationship with ''[[Falcarius]]'', a taxon that includes all the more derived therizinosauroids, however, it appears to be that ''Falcarius'' is more primitive than ''Beipiaosaurus''.<ref name=Zanno2010Falcarius>{{cite journal|last1=Zanno|first1=L. E.|date=2010|title=Osteology of Falcarius utahensis (Dinosauria: Theropoda): characterizing the anatomy of basal therizinosaurs|journal=Zoological Journal of the Linnean Society|volume=158|issue=1|pages=196–230|doi=10.1111/j.1096-3642.2009.00464.x|doi-access=free}}</ref><ref name=Zanno2010>{{cite journal|first1=L. E.|last1=Zanno|date=2010|title=A taxonomic and phylogenetic re-evaluation of Therizinosauria (Dinosauria: Maniraptora)|journal=Journal of Systematic Palaeontology|volume=8|issue=4|pages=503–543|doi=10.1080/14772019.2010.488045|url=https://www.researchgate.net/publication/229289268}}</ref>
The EBFFs of ''Beipiaosaurus'' are also unusually broad, up to 3&nbsp;mm wide in the type specimen. The broadest feathers of ''Sinosauropteryx'' are only 0.2&nbsp;mm wide, and only slightly wider in larger forms such as ''[[Dilong (dinosaur)|Dilong]]''. Additionally, where most primitive feather types are circular in cross section, EBFFs appear to be oval-shaped.


The cladogram below is the result of the performed phylogenetic analysis of the Therizinosauria by Hartman et al. 2019 which is largely based on the data provided by the revision of Zanno in 2010. ''Beipiaosaurus'' occupied a more derived position than ''Falcarius'', as previosuly indicated by Zanno:<ref name="Hartman2019">{{cite journal|last1=Hartman|first1=S.|last2=Mortimer|first2=M.|last3=Wahl|first3=W. R.|last4=Lomax|first4=D. R.|last5=Lippincott|first5=J.|last6=Lovelace|first6=D. M.|date=2019|title=A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flight|journal=PeerJ|volume=7|pages=e7247|doi=10.7717/peerj.7247|doi-access=free|pmid=31333906|pmc=6626525}}</ref>
None of the preserved EBFFs were curved or bent beyond a broad arc in either specimen, indicating that they were fairly stiff. They were probably hollow, at least at the base.
{{clade|style=font-size:100%; line-height:100%;

|label1='''[[Therizinosauria]]'''
In a 2009 interview, Xu stated: "Both [feather types] are definitely not for flight, inferring the function of some structures of extinct animals would be very difficult, and in this case, we are not quite sure whether these feathers are for display or some other functions." He speculated that the finer feathers served as an insulatory coat and that the larger feathers were ornamental, perhaps for social interactions such as mating or communication.<ref name="Bryner09"/>
|1={{clade

|1=''[[Falcarius]]'' [[File:F. utahensis reconstruction (flipped).jpg|70px]]
==Phylogeny and classification==
|2={{clade
''Beipiaosaurus'' was first assigned to the [[Therizinosauroidea]], in a basal position, by Xu ''et al.'' (1999). All subsequent [[phylogenetic]] analyses have confirmed this assignment. According to the definition by [[Paul Sereno]] of this group, ''Beipiaosaurus'' is even by definition the basal most member. Zanno (2010b) noted that ''Beipiaosaurus'' shares a sister-taxon relationship with a taxon that includes all the more derived therizinosauroids.<ref name=zanno10>{{cite journal | last1 = Zanno | first1 = L. E. | year = 2010 | title = Osteology of Falcarius utahensis (Dinosauria: Theropoda): characterizing the anatomy of basal therizinosaurs | url = | journal = Zoological Journal of the Linnean Society | volume = 158 | issue = 1| pages = 196–230 | doi=10.1111/j.1096-3642.2009.00464.x| doi-access = free }}</ref> Zanno also concluded that there is a genus that is less derived than ''Beipiaosaurus'', the genus ''Falcarius'', which is a basal [[Therizinosaur#Systematics|therizinosaurian]].
|1=''[[Jianchangosaurus]]''

|2={{clade
The following is a [[cladogram]] based on the phylogenetic analysis conducted by Lindsay E. Zanno in 2010, showing the relationships of ''Beipiaosaurus'':<ref name=zanno10/>
|1='''''Beipiaosaurus''''' [[File:Beipiaosaurus Restoration.png|70px]]

|2={{clade
{{clade| style=font-size:90%;line-height:80%
|1=''"[[Chilantaisaurus]]" zheziangensis''
|label1='''Therizinosauria'''
|2=''[[Enigmosaurus]]'' [[File:Enigmosaurus Restoration.jpg|70px]]
|3=''[[Alxasaurus]]''
|4={{clade
|1={{clade
|1={{clade
|1={{clade
|1='''[[Therizinosauridae]]''' [[File:Therizinosaurus Restoration.png|80px]] }} }} }} }} }} }} }} }}
|1=''[[Falcarius]]''
|label2='''Therizinosauroidea'''
|2={{clade
|1=''Beipiaosaurus''
|label2=<span style="color:white;">unnamed</span>
|2={{clade
|1=''[[Alxasaurus]]''
|label2=<span style="color:white;">unnamed</span>
|2={{clade
|1=''[[Erliansaurus]]''
|label2= <span style="color:white;">unnamed</span>
|2={{clade
|1=''[[Neimongosaurus]]''
|label2= <span style="color:white;">unnamed</span>
|2={{clade
|1=''[[Enigmosaurus]]''
|label2= <span style="color:white;">unnamed</span>
|2={{clade
|1=''[[Suzhousaurus]]''
|label2=[[Therizinosauridae]]
|2={{clade
|1=''[[Nanshiungosaurus]]''
|2=''[[Segnosaurus]]''
|3=''[[Erlikosaurus]]''
|4=''[[Therizinosaurus]]''
|label5=''[[Nothronychus]]''
|5={{clade
|1=''[[Nothronychus mckinleyi]]''
|2=''[[Nothronychus graffami]]'' }} }} }} }} }} }} }} }} }} }}


==Paleoecology==
==Paleoecology==
Studies suggest that the [[natural environment|paleoenvironment]] of the [[Yixian Formation]] involved seasonal climate fluctuations, and was warm and humid, punctuated by dry seasons, in which the environment became more arid.<ref name=wangetal2006conifer>{{cite journal|last1=Wang|first1=Y.|last2=Zheng|first2=S.|last3=Yang|first3=W.|last4=Zhang|first4=W.|last5=Ni|first5=Q.|date=2006|title=The biodiversity and palaeoclimate of conifer floras from the Early Cretaceous deposits in western Liaoning, northeast China|journal=International Symposium on Cretaceous Major Geological Events and Earth System|pages=56A}}</ref> The average yearly temperature during the time of ''Beipiaosaurus'' was {{convert|10|C}}, with relatively cold winters for the generally warm Mesozoic era.<ref name=amoitetal2011>{{cite journal|last1=Amiot|first1=R.|last2=Wang|first2=X.|last3=Zhou|first3=Z.|last4=Wang|first4=X.|last5=Buffetaut|first5=E.|last6=Lécuyer|first6=C.|last7=Ding|first7=Z.|last8=Fluteau|first8=F.|last9=Hibino|first9=T.|last10=Kusuhashi|first10=N.|last11=Mo|first11=J.|last12=Suteethorn|first12=V.|last13=Wang|first13=Y.|last14=Xu|first14=X.|last15=Zhang|first15=F.|date=2011|title=Oxygen isotopes of East Asian dinosaurs reveal exceptionally cold Early Cretaceous climates|journal=Proceedings of the National Academy of Sciences|volume=108|issue=13|pages=5179–5183|doi=10.1073/pnas.1011369108|doi-access=free|pmid=21393569|pmc=3069172}}</ref> A study by Wu et al. 2013 concluded that [[orbital forcing]], which is the effect on climate caused by shifts in the tilt of the Earth's axis and by the shape of the Earth's orbit, contributed to the climate fluctuations of this formation.<ref>{{cite journal|last1=Wu|first1=H.|last2=Zhang|first2=S.|last3=Jiang|first3=G.|last4=Yang|first4=T.|last5=Guo|first5=J.|last6=Li|first6=H.|date=2013|title=Astrochronology for the Early Cretaceous Jehol Biota in Northeastern China|journal=Palaeogeography, Palaeoclimatology, Palaeoecology|volume=385|pages=221–228|doi=10.1016/j.palaeo.2013.05.017}}</ref>


The Yixian Formation is well known for its great diversity of well-preserved specimens and its dinosaurs, such as the tyrannosauroids ''[[Dilong (dinosaur)|Dilong]]'' and ''[[Yutyrannus]]'', the dromaeosaurids ''[[Sinornithosaurus]]'', oviraptorosaurs including ''[[Caudipteryx]]'', compsognathids including ''[[Sinocalliopteryx]]'', avialans including ''[[Confuciusornis]]'' and some non-theropod dinosaurs, such as ''[[Psittacosaurus]]'' and ''[[Dongbeititan]]''.<ref name="zhou2006"/><ref name=Xu2020>{{cite journal|last1=Xu|first1=X.|last2=Zhou|first2=Z.|last3=Wang|first3=Y.|last4=W|first4=M.|date=2020|title=Study on the Jehol Biota: Recent advances and future prospects|journal=Science China Earth Sciences|volume=63|issue=6|pages=757–773|doi=10.1007/s11430-019-9509-3}}</ref>
===Fauna and habitat===
Studies suggest that the [[natural environment|paleoenvironment]] of the Yixian Formation involved seasonal climate fluctuations, and was warm and humid, punctuated by dry seasons, in which the environment became more arid.<ref name=wangetal2006conifer>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'', 56A.</ref> The average yearly temperature during the time of ''Beipiaosaurus'' was {{convert|10|C}}, with relatively cold winters for the generally warm Mesozoic era.<ref name=amoitetal2011>{{cite journal | last1 = Amiot | first1 = R. | last2 = Wang | first2 = X. | last3 = Zhou | first3 = Z. | last4 = Wang | first4 = X. | last5 = Buffetaut | first5 = E. | last6 = Lécuyer | first6 = C. | last7 = Ding | first7 = Z. | last8 = Fluteau | first8 = F. | last9 = Hibino | first9 = T. | last10 = Kusuhashi | first10 = N. | last11 = Mo | first11 = J. | last12 = Suteethorn | first12 = V. | last13 = Wang | first13 = Y. | last14 = Xu | first14 = X. | last15 = Zhang | first15 = F. | year = 2011 | title = Oxygen isotopes of East Asian dinosaurs reveal exceptionally cold Early Cretaceous climates | journal = Proceedings of the National Academy of Sciences | volume = 108 | issue = 13| pages = 5179–5183 | doi = 10.1073/pnas.1011369108 | pmid=21393569 | pmc=3069172}}</ref> A study by Wu et al. (2013) concluded that [[orbital forcing]], which is the effect on climate caused by shifts in the tilt of the Earth's axis and by the shape of the Earth's orbit, contributed to the climate fluctuations of this formation.<ref>{{cite journal | last1 = Wu | first1 = Huaichun | last2 = Zhang | first2 = Shihong | last3 = Jiang | first3 = Ganqing | last4 = Yang | first4 = Tianshui | last5 = Guo | first5 = Junhua | last6 = Li | first6 = Haiyan | year = 2013 | title = Astrochronology for the Early Cretaceous Jehol Biota in Northeastern China | url = | journal = Palaeogeography, Palaeoclimatology, Palaeoecology | volume = 385| issue = | pages = 221–228| doi = 10.1016/j.palaeo.2013.05.017 }}</ref>

The Yixian Formation is well known for its great diversity of well-preserved specimens and its dinosaurs, such as the tyrannosauroid ''[[Dilong (dinosaur)|Dilong]]'', the dromaeosaurid ''[[Sinornithosaurus]]'', oviraptorosaurs including ''[[Caudipteryx]]'', compsognathids including ''[[Sinocalliopteryx]]'', avialans including ''[[Confuciusornis]]'' and some non-theropod dinosaurs, such as ''[[Psittacosaurus]]'' and ''[[Dongbeititan]]''.


Other contemporaries of ''Beipiaosaurus'' included ancient shrimp, snails and slugs, as well as a diverse group of insects, and fish such as ''[[Lycoptera]]''. Most vertebrates in this formation showed a tendency to become [[arboreal]], including many tree-dwelling birds, and climbing mammals and lizards.<ref name="zhou2006"/> The flora was dominated by conifers related to modern species that are found mainly in [[subtropical]] and [[temperate]] upland forests, with the presence of ferns, cycads, and horsetails.
Other contemporaries of ''Beipiaosaurus'' included ancient shrimp, snails and slugs, as well as a diverse group of insects, and fish such as ''[[Lycoptera]]''. Most vertebrates in this formation showed a tendency to become [[arboreal]], including many tree-dwelling birds, and climbing mammals and lizards. The flora was dominated by conifers related to modern species that are found mainly in [[subtropical]] and [[temperate]] upland forests, with the presence of ferns, cycads, and horsetails.<ref name="zhou2006"/><ref name=wangetal2006conifer/><ref name=Xu2020/>


==See also==
==See also==
{{Portal|Dinosaurs}}
{{Portal|Dinosaurs}}
*''[[Nothronychus]]'' and ''[[Falcarius]]'' for additional primitive [[therizinosauridae|therizinosaur]] discoveries.
* [[Timeline of therizinosaur research]]
* [[Timeline of therizinosaur research]]
*''[[Falcarius]]''


==References==
==References==
Line 113: Line 88:
==External links==
==External links==
* [https://web.archive.org/web/20050308213846/http://www.dinosauria.com/jdp/archie/therizin.html Dinosauria] - News of the first ''Beipiaosaurus'' discovery.
* [https://web.archive.org/web/20050308213846/http://www.dinosauria.com/jdp/archie/therizin.html Dinosauria] - News of the first ''Beipiaosaurus'' discovery.
* [https://www.deviantart.com/dinomaniac/art/Beipiaosaurus-skeletal-117285354 Skeletal restoration]
* [http://www.ucmp.berkeley.edu/diapsids/saurischia/therizinosauroidea.html Therizinosauroidea - UCMP, Berkeley]
* [http://www.ucmp.berkeley.edu/diapsids/saurischia/therizinosauroidea.html Therizinosauroidea - UCMP, Berkeley]



Revision as of 17:33, 11 June 2020

Beipiaosaurus
Temporal range: Early Cretaceous,
~125 Ma
Components of the holotype specimen (prior to the caudal vertebrae re-excavation)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Clade: Therizinosauria
Superfamily: Therizinosauroidea
Genus: Beipiaosaurus
Xu et al. 1999
Type species
Beipiaosaurus inexpectus
Xu et al. 1999

Beipiaosaurus /ˌbpjˈsɔːrəs/ is a genus of therizinosauroid theropod dinosaurs that lived in Asia during the Early Cretaceous in the Yixian Formation. The first remains were found in 1996 and formally described in 1999. Before the discovery of Yutyrannus, they were among the largest dinosaurs known from direct evidence to be feathered. Beipiaosaurus is known from three reported specimens preserving numerous impressions of feather structures that allowed to determine the feathering color which turned out to be brownish.

They were relatively small-sized therizinosaurs, measuring 2.2 m (7.2 ft) long and weighing about 45–91 kg (99–201 lb) in contrast to the advanced and giant Segnosaurus or Therizinosaurus. The necks of Beipiaosaurus were shorter than in most therizinosaurs, whose are characterized by elongated necks adapted for high-browsing. Also, their feet configuration differs from therizinosaurids, having a generic three-toed pes instead of four as seen in other members.

The exact classification of therizinosaurs had in the past been hotly debated, since their prosauropod-like teeth and body structure indicate that they were generally herbivorous, unlike typical theropods. Beipiaosaurus, being considered to be a primitive therizinosauroid, has features which suggest that all therizinosauroids, including the more derived Therizinosauridae, to be coelurosaurian theropods, not sauropodomorph or ornithischian relatives as once believed.

History of discovery

In 1996, the peasant Li Yinxian discovered a skeleton of a theropod dinosaur near the village of Sihetun. In the May 27, 1999, issue of the journal Nature the discovery was announced and the type species Beipiaosaurus inexpectus named and described by Xu Xing, Tang Zhilu and Wang Xiaolin. The generic name Beipiaosaurus translates as "Beipiao lizard" after Beipiao, a city in China near the location of its discovery. Beipiaosaurus is known from a single species, B. inexpectus, the specific name, meaning "unexpected" in Latin, referring to the"surprising features in these animals".[1]

Skeletal composite of IVPP V11559 and STM 31-1

The holotype (type specimen) of Beipiaosaurus inexpectus, IVPP V11559, was recovered in the Jianshangou Beds of the Yixian Formation in Liaoning Province, China. The specimen was collected in sediment deposited during the Aptian stage of the Early Cretaceous period, approximately 125 million years ago.[2] It is housed in the collection of the Institute of Vertebrate Paleontology and Paleoanthropology, in Beijing, China. It consists of a partial, sub-adult, skeleton that is largely disarticulated. A significant number of fossilized bones were recovered, including: cranial fragments, a mandible, teeth, three cervical vertebrae, four dorsal vertebrae, four dorsal ribs, two sacral vertebrae, twenty-five caudal vertebrae with a pygostyle, three chevrons, an incomplete furcula and scapula, both coracoids, both forelimbs, both ilia, an incomplete pubis, an incomplete ischium, a femur, both tibiae (one incomplete), an incomplete fibula, the astragalus and calcaneum, several tarsals, metatarsals, manual and pedal unguals, and skin impressions of the primitive plumage.[1][3] The pelvic girdle and caudal vertebrae were discovered during a re-excavation of the fossil quarry were the first elements of the holotype were found. These rediscovered elements helped to complete the holotype specimen.[3]

A second specimen, STM 31-1, a partial skeleton, was described by Xu et al. 2009, which preserves a significant covering of unique, elongated feathers. This specimen consisted of a complete skull, a sclerotic ring, the mandible, the atlas and axis bones, nine additional cervical vertebrae, dorsal vertebrae, seventeen cervical ribs, twelve dorsal ribs, both scapulae and coracoids, one complete humerus and proximal humerus, one complete radius and distal radius, one complete ulna and distal ulna, carpals, and some metacarpals. The rear of the skull of this specimen was badly crushed.[4] Li et al. 2014 mentioned a third specimen labelled under the number BMNHC PH000911. This specimen hails from the Sihetun locality at the Beipiao County in Liaoning Province and compromises a partial individual preserving the skull (badly crushed), most of the vertebral colum, both arms and other postcrania. Traces of feather integument were found around the neck area.[5]

Description

Size comparison between an average individual and a 1.8 m tall human

Beipiaosaurus were small-sized therizinosaurs, measuring 2.2 m (7.2 ft) in length, and before the discovery of Yutyrannus they were among the largest dinosaurs known from direct evidence to be feathered.[1] They are estimated to have weigh between 45 to 91 kg (99 to 201 lb).[6] More advanced therizinosaurids have four functional toes, but the feet of Beipiaosaurus still have reduced inner toes, showing that the derived therizinosaurid condition may have evolved from a three-toed therizinosauroid ancestor. The head was large relative to other therizinosaurs, with the lower jaw measuring about same length as the femur. The neck appears to be shorter compared to other therizinosaurs.[1][4] In 2003 the pygostyle, consisting of the fused five last vertebrae of the tail, was described in greater detail, suggesting that the original function of the pygostyle was not linked with pennaceous feathers.[3]

Distinguishing traits

According to Zanno in 2010, Beipiaosaurus can be distinguished from other therizinosaur taxa based on the following characteristics, which are unique derived traits (autapomorphies): a low ridge is present on the front of the thighbone shaft which extends upwards from the inner condyle; the last four dorsal vertebrae are fused; from at least the seventh vertebra onwards the tail vertebrae are fused into a pygostyle; a prominent triangular flange extends outwards, away from the body, from the underside of the first metacarpal; the skull is large, about as long as the thighbone; the first phalanx of the first digit has a joint surface with the claw, that is elongated in the direction of the finger tip on the outer side of its lower part; on the front edge of the ischium a projection, the obturator process, has a wavy profile with a tip that is curved downwards; the "boot" at the lower end of the ischium has twice the width, measured from the front to the rear, of the lower shaft of the ischium.[7]

In 2019 Liao and Xu redescribed the holotype skull in detail, noting new unique cranial traits for Beipiaosaurus. These consisted of the large postorbital joint of the frontal and its abrupt transition from the orbital edge, a long and keen anterior joint of the parietal, an elongate bottom branching of the squamosal articulation of the parietal, and the deeply external mandibular fenestra that is located towards the rear.[8]

Feathers and color

Feather impressions on the left arm from the holotype on display at the Paleozoological Museum of China

The first feather impressions were found in the holotype specimen, consisting of short, slender filamentous feathers on the left arm. These impressions indicated that the body was predominately covered by downy feather-like fibers, similar to those of Sinosauropteryx, but longer, and oriented perpendicular to the arm. Xu et al. 1999 suggested that these downy feathers represent an intermediate stage between Sinosauropteryx and more advanced birds (Avialae).[1] The tail was also covered in feathers between four and seven centimeters long, consisting of parallel filaments with a width of 1.5 mm (0.15 cm), without a trace of pennaceous feathers or a tail fan, as indicated by the preserved pygostyle.[3]

Unique among known theropods, Beipiaosaurus also possessed a secondary coat of much longer, simpler feathers that rose out of the down layer. These unique feathers known as EBFFs (elongated broad filamentous feathers) were first described by Xu et al. 2009, based on specimen STM 31-1 consisting of the torso, head and neck. Xu and his team also found EBFFs in the tail of the holotype IVPP V11559, which were revealed by further preparation. Some of these were damaged during preparation though.[4]

Diagram illustrating feather evolution stages. Beipiaosaurus falls within stage 1 and stage 2

The EBFFs differ from other feather types in that they consist of a single, unbranched filament. Most other primitive feathered dinosaurs have down-like feathers made up of two or more filaments branching out from a common base or along a central shaft. The EBFFs of Beipiaosaurus are also much longer than other primitive feather types, measuring about 100–150 mm (10–15 cm) long, roughly half the length of the neck. In Sinosauropteryx, the longest feathers are only about 15% of the neck length. The EBFFs of Beipiaosaurus are also unusually broad, up to 3 mm (0.30 cm) wide in the holotype. The broadest feathers of Sinosauropteryx are only 0.2 mm (0.020 cm) wide, and only slightly wider in larger forms such as Dilong. Additionally, where most primitive feather types are circular in cross section, EBFFs appear to be oval-shaped. None of the preserved EBFFs were curved or bent beyond a broad arc in either specimen, indicating that they were fairly stiff. They were probably hollow, at least at the base.[4]

In 2009 during a interview at Live Science, Xu stated: "Both are definitely not for flight, inferring the function of some structures of extinct animals would be very difficult, and in this case, we are not quite sure whether these feathers are for display or some other functions." He speculated that the finer feathers served as an insulatory coat and that the larger feathers were ornamental, perhaps for social interactions such as mating or communication.[9]

Life restoration

Li et al. 2014 compared the color and shape of the melanosomes in 181 extant animal specimens, 13 fossil specimens (including Beipiaosaurus) and previous data about the melanosome diversity using scanning electron microscopes. They found that color in dinosaurs seem to be slightly connected with their physiology. While some species of living reptiles (lizards or crocodiles, which are ectothermic) have less diversity in the shape of melanosomes and darker color ranges, some maniraptorans, birds and mammals (which are endothermic) have an increased diversity of melanosome shapes and more vivid colors. The examined specimen of Beipaosaurus, BMNHC PH000911, preserves feather impressions which are located in the neck area. These are filamentous/sparce in structure and the sampled melanosomes were sphere-shaped and inferred to had a brownish colouration like those in modern reptiles which fall within the range of dark brownish colourations.[5]

Jianchangosaurus is another primitive therizinosaur taxon known from the same formation that was found with impressions of a series of filamentous and unbranched feathers in its holotype specimen. Only the distal ends of the feather impressions are visible and based on their morphology the feathers are considered to be EBFFs, bearing resemblance to those found along the specimens of Beipiaosaurus. These findings suggest that they might have been used for visual display and were common among early therizinosaurs.[10]

Classification

Schematic comparison of the ilium of Beipiaosaurus (in B) and other related therizinosaurs

The affinities of therizinosaurs were originally obscure and often problematic, giving rise to taxonomic debate since they feature similar adaptations to the unrelated sauropodomorphs and ornithischians. The description of Beipiaosaurus helped to assemble the definitive placement of therizinosaurs within the Theropoda, especially as maniraptorans thanks to the numerous theropod features and irrefutable feather impressions in the holotype.[1]

Beipiaosaurus was first assigned to the Therizinosauroidea, in a very primitive position by Xu et al. 1999.[1] All subsequent phylogenetic analyses have confirmed this assignment. According to the definition by Paul Sereno of this group, Beipiaosaurus is even by definition the basal most member. Lindsay E. Zanno noted that Beipiaosaurus shares a sister-taxon relationship with Falcarius, a taxon that includes all the more derived therizinosauroids, however, it appears to be that Falcarius is more primitive than Beipiaosaurus.[11][7]

The cladogram below is the result of the performed phylogenetic analysis of the Therizinosauria by Hartman et al. 2019 which is largely based on the data provided by the revision of Zanno in 2010. Beipiaosaurus occupied a more derived position than Falcarius, as previosuly indicated by Zanno:[12]

Therizinosauria

Paleoecology

Studies suggest that the paleoenvironment of the Yixian Formation involved seasonal climate fluctuations, and was warm and humid, punctuated by dry seasons, in which the environment became more arid.[13] The average yearly temperature during the time of Beipiaosaurus was 10 °C (50 °F), with relatively cold winters for the generally warm Mesozoic era.[14] A study by Wu et al. 2013 concluded that orbital forcing, which is the effect on climate caused by shifts in the tilt of the Earth's axis and by the shape of the Earth's orbit, contributed to the climate fluctuations of this formation.[15]

The Yixian Formation is well known for its great diversity of well-preserved specimens and its dinosaurs, such as the tyrannosauroids Dilong and Yutyrannus, the dromaeosaurids Sinornithosaurus, oviraptorosaurs including Caudipteryx, compsognathids including Sinocalliopteryx, avialans including Confuciusornis and some non-theropod dinosaurs, such as Psittacosaurus and Dongbeititan.[2][16]

Other contemporaries of Beipiaosaurus included ancient shrimp, snails and slugs, as well as a diverse group of insects, and fish such as Lycoptera. Most vertebrates in this formation showed a tendency to become arboreal, including many tree-dwelling birds, and climbing mammals and lizards. The flora was dominated by conifers related to modern species that are found mainly in subtropical and temperate upland forests, with the presence of ferns, cycads, and horsetails.[2][13][16]

See also

References

  1. ^ a b c d e f g Xu, X.; Tang, Z.-L.; Wang, X. L. (1999). "A therizinosauroid dinosaur with integumentary structures from China". Nature. 339 (6734): 350–354. Bibcode:1999Natur.399..350X. doi:10.1038/20670. ISSN 1476-4687.
  2. ^ a b c 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.
  3. ^ a b c d Xu, X.; Cheng, Y.; Wang, X.-L.; Chang, C. (2003). "Pygostyle‐like Structure from Beipiaosaurus (Theropoda, Therizinosauroidea) from the Lower Cretaceous Yixian Formation of Liaoning, China". Acta Geologica Sinica. 77 (3): 294–298. doi:10.1111/j.1755-6724.2003.tb00744.x.
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