Rare clouds that glow in the dark are the most vibrant in 15 years for sky watchers in the upper US, Canada and Europe
- Noctilucent clouds were spotted the US, Canada and parts of Europe over the weekend
- Experts say this is the first time such a vivid display has been seen in nearly 15 years
- The clouds form in the mesosphere, which is at altitudes of around 50 miles, when ice clouds interact with the sun that is shining just below the horizon
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The rarest clouds on Earth were spotted by sky watchers in parts of western US, Europe and Canada over the weekend a vibrant display that has not been seen in about 15 years.
Known as noctilucent, these clouds were glowing a stunning blue in the sky just after the sun moved below the horizon.
Reports of the eerie-looking clouds came from Oregon, Washington, Alberta, the UK and Denmark.
Noctilucent clouds (NLCs) form in the mesosphere, which is at altitudes of around 50 miles – making them the highest in Earth’s atmosphere.
The clouds consist of ice crystals that become visible during twilight when the sun is shining from blow the horizon.
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‘There’s really nothing else quite like them,’ the National Weather Service office in Seattle wrote on social media, noting that these are the ‘most vivid displays of noctilucent clouds’ that have been seen in decades in the area.
The clouds typically form in late spring and early summer when the lower atmosphere becomes warmer.
Atmospheric circulation pushes air upwards, which then expands and cools.
Water vapor becomes trapped in the clouds, freezes into ice crystals and forms meteoric dust.
The clouds appear with electric blue and silver streaks and are typically spotted at latitudes of 45 and 80 degrees in the northern and southern hemispheres.
And the stunning display can even be seen from space, as astronauts aboard the International Space Station have shared pictures of the phenomenon.
There is some belief that climate change is also contributing to their development and even to them being seen at latitudes never seen before.
For example, in 2019, they were seen as far south as Joshua Tree, California, which suggests that with more greenhouse gases in the atmosphere, there is more water vapor available for the glowing clouds to form.
Cora Randall, a professor at the University of Colorado Boulder, told The Washington Post that the increase in clouds could be due to excessive water vapor in the atmosphere from rocket launches.
Another study suggests that the appearance of NLCs does fluctuate from year to year and even from decade to decade, but that overall, they have become ‘significantly’ more visible.
In 2020, a photographer shared a stunning image of the phenomenon in the early morning hours that gave a 12th century church a ghostly glow.
Ollie Taylor, an astrophotographer, snapped ‘night-shining’ clouds that lit up the night sky in southwest England with spectacular streaks of blue and silver.
On June 22, Taylor set out on a mission to capture the night-shining clouds in Dorset, which sits on the south coast of England.
He arrived at the Knowlton Church in the middle of a Neolithic monument and started snapping the scene starting at 2am to 2:50am.
‘It was an excellent night of shooting, arriving at location in the evening already greeted by noctilucent clouds better than I had previously seen in the south of England,’ said Taylor.
‘The electric blue complemented the misty landscape and eerie structure.’
Taylor tracked the clouds using a combination of different sources, including space weather updates, webcam observations and a Facebook group, according to the European Space Agency.
Noctilucent clouds were first described in the mid-19th century after the eruption of Krakatau.
Volcanic ash spread through the atmosphere, making for vivid sunsets around the world and provoking the first known observations of NLCs.
At first people thought they were a side effect of the volcano, but long after Krakatau’s ash settled, the wispy, glowing clouds remained.
WHAT ARE NOCTILUCENT (NIGHT-SHINING) CLOUDS?
Noctilucent clouds, also called polar mesospheric clouds, form between 47-53 miles above Earth’s surface (76-85 km), according to NASA.
Here, water vapor freezes into clouds of ice crystals, which are illuminated when the sun is below the horizon.
They are seeded by debris from disintegrating meteors, giving them a ‘shocking’ blue hue when they reflect sunlight.
The clouds are formed during the summer of both the northern and southern hemispheres.
Perseids meteor shower: Where you need to go in Alberta to see it | CTV News – CTV News Calgary
While a supermoon is expected to wash out all but the very brightest of this year’s Perseids meteor shower, astronomy experts say if you choose your spot well, you will still be able to enjoy it.
The Perseids meteor shower is expected to peak on Aug. 12 and 13 and that is when the best viewing period will be.
Gary Boyle, educator and writer with the Wonders of Astronomy, says a comet that last passed through the solar system 30 years ago causes the phenomenon.
“A meteor shower is caused by a comet’s debris – we’re plowing through the dusty tail of comet Swift-Tuttle that last went around the sun and moon in 1992,” he said in an interview with CTV News on Thursday.
“Just like going through a rain storm or hitting a cloud of bugs in the summertime with your windshield, we’re just going through the thickest part of the cloud which usually gives us about 90 meteors per hour – but it’ll be a little different this year because of the moon.”
This year, August’s moon is full, large and very bright – enough to make it like there are city lights on even out in rural areas.
“That 90 per hour will dwindle to about 20 or 30 of the brighter ones,” Boyle said, adding that even without the full show, it’s still a good time to get outside.
There are three planets visible each night, Boyle says – Saturn, which is most visible at sunset, then two hours later Jupiter and two hours after that, he says Mars will be visible.
However, you likely won’t be able to see anything while within city limits, he says.
“It’s best to get outdoors, away from city lights if you can, out in the countryside to get that full 360-degree terrain.”
Boyle says that while the meteors do come from the northeast, they could streak through the atmosphere at 60 km/s “in any and all directions.”
“That’s why, if you have different people looking in different directions, someone’s bound to see something.”
More information on stargazing in southern Alberta can be found online.
IAU XXXI General Assembly draws to a close – EurekAlert
The XXXI General Assembly of the International Astronomical Union (IAU) ends today in Busan, Korea. Having been postponed by one year due to the COVID-19 pandemic, the meeting took place as the first hybrid General Assembly, with around 1200 in-person participants and around 700 attending online. The conference included seven symposia, 10 multi-session Focus Meetings, as well as many more meetings of IAU Divisions, Commissions and Working Groups.
The XXXI IAU General Assembly in Busan, Korea, ends today, Thursday 11 August 2022, after two busy weeks packed with scientific talks and meetings. Despite facing ongoing challenges due to COVID-19, the conference was a great success, thanks to the dedication of the Local Organising Committee. As well as being the first IAU General Assembly to be held in Korea, this meeting was also the first to have a hybrid format, with around 1200 participants attending in person and around 700 joining online.
Conference attendees enjoyed a wide range of presentations, not only on technical subjects within subdisciplines of astronomy, but also on bigger-picture development, advancement and collaboration within astronomy. There were seven symposia, 10 Focus Meetings and many more meetings organised by the IAU Offices as well as the Divisions, and Executive Committee Working Groups.
The programme also featured a number of invited discourses and public lectures. Topics included the early science being done with the James Webb Space Telescope; the state of the Universe according to our current understanding; the imaging of supermassive black holes with the Event Horizon Telescope; and how the seemingly contradictory measurements of the Hubble constant might be resolved.
Besides the scientific programme, participants had the opportunity to join a star party at BEXCO, the huge conference venue in Busan, and several tours of the local area around the region. Korean culture was weaved into the conference itself, with the opening ceremony featuring a performance of traditional Korean dance.
Highlights of all aspects of the programme, from scientific meetings to public lectures and sightseeing opportunities were collected in the e-Newspaper (http://www.iau.org/static/publications/ga_newspapers/20220810.pdf), published every day of the conference.
The General Assembly also saw the launch of the NameExoWorlds 2022 Competition (https://www.iau.org/news/pressreleases/detail/iau2209/) to celebrate the 10th anniversary of the IAU Office of Astronomy for Development (OAD) (https://www.astro4dev.org/). This contest invites everyone around the world to propose names for 20 exoplanets and their host stars, which will be among the first targets of the James Webb Space Telescope.
Another major topic of discussion at the meeting was the new Center for the Protection of the Dark and Quiet Sky from Satellite Constellation Interference (CPS) (https://cps.iau.org/), which was established in April this year. This new centre aims to mitigate against the interference of new satellite constellations in optical and radio astronomy, and contributors had new results of observations to share during the conference.
Since this General Assembly was postponed by one year, the four IAU Officers of the current triennium have already taken up their roles. However, the officers from both this triennium and the previous one took part in the opening ceremony.
The four IAU Officers in the current triennium are:
1. President: Debra Meloy Elmegreen
2. General Secretary: José Miguel Rodriguez Espinosa
3. President Elect: Willy Benz
4. Assistant General Secretary: Diana Mary Worrall
Unusually for a General Assembly, no Business Meetings were held and no Resolutions were presented to be voted on, as this was all done virtually in 2021. There was an online vote during the meeting, in which National Members voted to admit Georgia (https://www.iau.org/administration/membership/national/members/71/) as a new National Member.
Although new Individual and Junior Members are normally announced at the General Assembly, this year they were announced (https://www.iau.org/news/announcements/detail/ann22025/) in June, bringing the number of Junior Members to over 1000 for the first time and the total to around 12,500 members.
The closing ceremony included the flag handover to Cape Town, South Africa, where the XXXII IAU General Assembly will be hosted. It will take place in 2024 after a gap of just two years instead of three, owing to the postponement of the XXXI General Assembly. The location of the XXXIII General Assembly in Rome, Italy was also announced.
Eight issues of the General Assembly newspaper were published during the meeting, and are available to read in full online (http://www.iau.org/static/publications/ga_newspapers/20220810.pdf). Press releases can be found in the press releases archive (https://www.iau.org/news/pressreleases/). Images from the meeting can be viewed in the online gallery (https://www.iau.org/public/images/archive/category/general_assembly_2022/). More information about the XXXI IAU General Assembly is available on the website (https://www.iauga2022.org/).
The IAU is the international astronomical organisation that brings together more than 12 000 active professional astronomers from more than 100 countries worldwide. Its mission is to promote and safeguard astronomy in all its aspects, including research, communication, education and development, through international cooperation. The IAU also serves as the internationally recognised authority for assigning designations to celestial bodies and the surface features on them. Founded in 1919, the IAU is the world’s largest professional body for astronomers.
* IAU GA 2022 external website – https://www.iauga2022.org/
* IAU GA 2022 image gallery – https://www.iau.org/public/images/archive/category/general_assembly_2022/list/2/
* IAU GA 2022 e-Newspaper – http://www.iau.org/static/publications/ga_newspapers/20220810.pdf
Lars Lindberg Christensen
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A new Cretaceous thyreophoran from Patagonia supports a South American lineage of armoured dinosaurs | Scientific Reports – Nature.com
The early evolution of thyreophoran dinosaurs is thought to have occurred primarily in northern continents since most evidence comes from the Lower and Middle Jurassic of Europe and North America. The diversification into stegosaurs and ankylosaurs is obscured by a patchy fossil record comprising only a handful of fragmentary fossils, most with uncertain phylogenetic affinities. Here we report the discovery of a new armoured dinosaur from the early Late Cretaceous of Argentina, recovered phylogenetically using various datasets either as a basal thyreophoran or a stem ankylosaur, closely related to Scelidosaurus. It bears unusual anatomical features showing that several traits traditionally associated with the heavy Cretaceous thyreophorans did not occur universally. Jakapil kaniukura gen. et sp. nov. is the first definitive thyreophoran species from the Argentinian Patagonia. Unlike most thyreophorans, it seems to show a bipedal stance, as in Scutellosaurus. Jakapil also shows that early thyreophorans had a much broader geographic distribution than previously thought. It is a member of an ancient basal thyreophoran lineage that survived until the Late Cretaceous in South America.
Thyreophora is a clade of ornithischian dinosaurs characterized by the presence of dermal bone armour on their backs1. Although most thyreophorans are grouped within Eurypoda (Ankylosauria + Stegosauria), basal thyreophorans show unresolved phylogenetic placements. Traditionally, they have been recovered as non-eurypodan thyreophorans2,3,4,5. Alternatively, new research suggests them as non-ankylosaurian ankylosauromorphs6 (also suggested by Refs.7,8). The most representative of these forms are Scutellosaurus, Emausaurus and Scelidosaurus, from the Lower Jurassic of the USA, Germany and England, respectively. Scutellosaurus is a small (1.5–2 m body length) and slender thyreophoran with a bipedal life style9 whereas the larger Scelidosaurus (4.5 m body length) is thought to be facultatively bipedal10 (body length has not been confidently estimated for Emausaurus). Both Scutellosaurus and Scelidosaurus represent part of the early locomotor diversity of early ornithischians, with obligate quadrupedality evolving in later and larger ankylosaurs and stegosaurs9.
The fossil record of Thyreophora is mainly known from the northern hemisphere, and its presence in the Gondwanan continents remains poorly known, with only a few ankylosaurian or stegosaurian species, and several indeterminate materials4,11,12,13,14,15.
We present here a new thyreophoran genus and species from the Late Cretaceous of South America. The remains were found near the locality of Cerro Policía within the ‘La Buitrera Paleontological Area’ (LBPA), close to the E. Ramos Mexía Dam, in North Patagonia, Río Negro Province, Argentina. The outcrops exposed in the LBPA represent the upper section of the Candeleros Formation (Cenomanian). They are interpreted as aeolian accumulations of the Kokorkom Desert (a ~ 826 km2 paleoerg16), with shifts between arid and semi-arid climatic conditions17. Most fossils in the LBPA were found between beds of migrating dunes. The new specimen was found as a close association of elements in a small area (~ 1.5 m × 1 m), isolated from any other individual, as generally occurs in the Candeleros Formation in the LBPA. The remains were found disarticulated, and with a slight southwestern-northeastern orientation due to dune transport.
The LBPA comprises a few localities such as La Buitrera, Cerro Policía, La Escondida and El Pueblito. This rich fossiliferous site produces three-dimensional, largely undeformed fossil vertebrates, including theropod dinosaurs18, uruguaysuchid crocodyliforms19, eilenodontine sphenodontians20, limbed snakes21, lizards22, chelid turtles23, dryolestoid mammals24, dipnoans16 and undescribed pterosaurs. Fragmentary sauropod skeletons and dinosaur tracks have also been recorded16. This new thyreophoran discovery from the LBPA provides new information about the structure of the early Late Cretaceous North Patagonian communities and the role of the still poorly known ornithischian component. In addition, this specimen provides new information about the early diversification and distribution of this cosmopolitan group.
AMNH, American Museum of Natural History, New York, USA; BRSMG: Bristol City Museum, Bristol, England; NHMUK: Natural History Museum, London, England; MNA: Museum of Northern Arizona, Flagstaff, USA; MPCA-PV: Colección de Paleovertebrados, Museo Provincial Carlos Ameghino, Cipolletti, Argentina; ZMNH: Zhejiang Museum of Natural History, Hangzhou, China.
The genus, Jakapil (Ja-Kapïl: shield bearer), comes from the ‘gananah iahish’, Puelchean or northern Tehuelchean language. The specific epithet, comprising kaniu (crest) and kura (stone), refers to the diagnostic ventral crest of the mandible, and comes from the Mapudungun language. These languages, currently spoken by more than 200,000 people, have been combined as a tribute to both of the coexisting native populations of North Patagonia, South America.
MPCA-PV-630 is a partial skeleton of a subadult individual (see Supplementary Information) that preserves fragments of some cranial bones (premaxilla, maxilla and basisphenoid), approximately 15 partial teeth and fragments, a nearly complete left lower jaw plus an isolated surangular, 12 partial vertebral elements, a complete dorsal rib and fifteen rib fragments, a partial coracoid, a nearly complete left scapula, a partial right scapula, two partial humeri, a possible partial right ulna, a complete and a partial metacarpal bone, three ischial and two femoral fragments, the distal end of a right tibia, the proximal end of a right fibula, three pedal phalanges, and more than forty osteoderms.
MPCA-PV-371, two partial conical osteoderms.
Locality and horizon
Upper beds of the Candeleros Formation, early Late Cretaceous (Cenomanian, ~ 94–97 My, see16, and references therein), locality of Cerro Policía, Río Negro Province, North Patagonia, Argentina (Suppl. Fig. 1).
Jakapil differs from all other thyreophorans in having: a large, ventral crest on the posterior half of the lower jaw, which is composed of the dentary, the angular and the splenial (medially hidden by the crest); a dorsomedially directed process in the short retroarticular process; leaf-shaped tooth crowns with a prominent mesial edge on their labial surface; maxillary and dentary tooth crowns differ from each other in their apical contour, the former being pointed and strongly asymmetrical, and the latter slightly curved distally with a more rounded and less asymmetrical contour; elongated (articular surface almost or completely beyond the posterior centrum face) and slender (width of less than a half postzygapophyses length) postzygapophyses in dorsal vertebrae; a strongly reduced humerus relative to the femur (proximal humeral width smaller than distal femoral width, see Supplementary Information), with a deep proximal fossa distally delimited by a curved ridge; a very large fibula relative to the femur (anteroposterior length of the proximal end almost comparable to the distal width of the femur); flattened and thin disk-like postcranial osteoderms.
A detailed description of the holotype is provided in the Supplementary Information. Jakapil is a small thyreophoran dinosaur (the subadult holotype is estimated to have been less than 1.5 m in body length and to have weighed 4.5–7 kg; see Supplementary Information, femoral description), with several novelties for a thyreophoran dinosaur.
A short skull is suggested by the size of the skull and jaw bones, and the reduced number of dentary tooth positions (eleven), compared with most non-ankylosaurid thyreophorans28,29. The antorbital and mandibular fenestrae seem absent, as in ankylosaurs29 (Fig. 1a; the mandibular fenestra is also absent in Scelidosaurus10). Dentary and maxillary emarginations are present, as usual in ornithischians30 (Fig. 1a). The block-like basisphenoid is strongly similar to that of Scelidosaurus10, with Vidian canals opened posterodorsally to the basipterygoid processes, the basipterygoid processes lateroventrally projected (unlike the anteriorly directed processes of stegosaurs28 and ankylosaurs29), and a strong cultriform process (as in Lesothosaurus31, Thescelosaurus32 and probably Scelidosaurus10; Fig. 1b).
Jakapil also bears the first predentary bone (Fig. 2a–d) with a plesiomorphic shape in a thyreophoran. It is subtriangular and quite similar to that of Lesothosaurus31, and externally it is ornamented by sulci and foramina, suggesting the presence of a keratinous beak. A beak is also supported in the edentulous and subtly ornamented preserved part of the premaxilla, as in derived thyreophorans28,29. The posterior half of the short lower jaw (Fig. 2a–f) is strongly dorsoventrally expanded, resembling the general shape of the heterodontosaurid33 and basal ceratopsian jaws34. This expansion is composed of a well-developed coronoid eminence (Fig. 2a–d, ce; similar to that in the stegosaur Huayangosaurus35 and most ankylosaurs36) and a large ventral crest at the dentary-angular contact that is unique among thyreophorans (Fig. 2a–d,f, vmc; resembling that of some ceratopsians, see SI). The dentary symphysis is slightly spout-shaped, as in most ornithischians37. Anteriorly, the dentary oral margin is subhorizontal in lateral view (Fig. 2a–d, D), unlike the strongly downturned line of most thyreophorans30,37. There is no evidence of a mandibular osteoderm as occurs in Scelidosaurus and ankylosaurs10. A surangular tubercle (Fig. 2a, st) adjacent to the glenoid fossa seems anteriorly continued by a subtly developed subhorizontal inflection of the anterior lamina (Fig. 2e, hi), in the position of the surangular ridge (synapomorphy of Thyreophora37), though the first is poorly developed. The glenoid fossa is roughly aligned with the tooth row in lateral view (Fig. 2a–d). The short retroarticular process bears a dorsomedially directed process resembling that of several theropods (Fig. 2g, dmp; see Discussion). This process is absent in all other thyreophorans 9,10,35,36.
The tooth crowns are leaf-shaped as in basal ornithischian and thyreophorans10,28,29,38 (Fig. 3). The tooth crowns are swollen labially at their base and lack both cingulum and ornamentation, unlike those of derived eurypodans28,29, heterodontosaurids33 and most neornithischians30,32. The mesial edge of the labial surface in the maxillary and dentary tooth crowns is prominent as in Scelidosaurus10, and ends distally in a denticle-like structure in Jakapil (Fig. 3, me). This prominent edge delimits anteriorly the wear facets of the dentary teeth. A striking difference with respect to most thyreophorans is that the maxillary and dentary tooth crowns are quite different (see Supplementary Information). The maxillary teeth (Fig. 3a–d) show seven/eight mesial and four distal denticles, a vertical apical denticle, and a straighter mesial denticle row (resembling those of non-ankylosaurid and non-stegosaurid thyreophorans10,35,36). The dentary teeth (Fig. 3e–j) bear seven mesial and five/six distal denticles, and a distally curved apical-most denticle. Also, the mesial denticle row is lingually recurved, as in Huayangosaurus35. Large, high-angled wear facets are present (Fig. 3d,h,j; dwf and mwf).
The axial elements are similar to those of Scelidosaurus39 (Fig. 4). The posterior articular surface of an isolated cervical centrum is flattened and seems almost as wide as high. A large foramen is placed just posteroventral to the parapophysis. The dorsal centra are cylindrical and elongated, with subcircular articular surfaces, and are biconcave (Fig. 4c,e). The neural arch is low but the neural canal is larger (Fig. 4d,e, nc). A dorsal neurocentral suture is visible (Fig. 4c, ncs). The diapophyses are laterodorsally directed almost 40° from the horizontal (Fig. 4d, di), at a lower angle than in stegosaurs28 and most ankylosaurs29, unlike the horizontal processes of basal ornithischians38. The postzygapophyses are medially fused in a slender (width of less than a half postzygapophyses length) and strongly elongated posteriorly structure (Fig. 4b, poz; more than in some ankylosaurs, such as Euoplocephalus and Polacanthus; see40,41). An isolated mid-caudal vertebra shows an equidimensional centrum in lateral view, with concave, oval articular surfaces (Fig. 4g). Transverse processes are very small and button-like (Fig. 4g, tp). Postzygapophyses are medially fused and do not extend beyond the centrum edge (Fig. 4g, poz). Proximally, the cross-section of the dorsal ribs is T-shaped. The low curvature of the shaft suggests a wide torso, as occurs in Emausaurus42, Scelidosaurus39, and ankylosaurs29. Some rib fragments with expanded (though broken) posterior edges suggest the presence of intercostal bones (Fig. 4h, ebr), as in Scelidosaurus39, Huayangosaurus43,44, some ankylosaurids45 (and references therein) and some basal ornithopods46. Some ribs are distally expanded (Fig. 4i) like the anterior dorsal ribs of Scelidosaurus39 and Huayangosaurus43.
Girdle and limb bones (see also Suppl. Figs. 2, 3) are mostly broken and with boreholes (probably due to bioerosion) at their ends. The scapular blade (Fig. 4j, sb) is elongated and parallel-sided, without distal expansion, an overall shape that resembles that of several theropods47, contrasting the distally expanded condition in most ornithischians30. A straight and parallel sided scapular blade is common in ankylosaurids29,40. The proximal scapular plate with a high acromial process (Fig. 4j,k, ap) is stegosaurian-like, and the lateral acromial crest (Fig. 4j,k, ac) is developed as in Huayangosaurus43. A low distinct ridge rises posterior to the glenoid fossa and represents the insertion site for the muscle triceps longus caudalis, as occur in ankylosaurids 40. The incomplete coracoid (Fig. 4l) is much shorter than the scapula, unlike that of ankylosaurs29,40, which bear a large coracoid. The coracoid and the scapula are not fused. The partial humeri (Fig. 3m) are strongly reduced in size, with overall limb proportions resembling those of basal ornithischians3,38 and several theropods47. A possible proximal end of the ulna (Fig. 4n) resembles that of other basal ornithischians, though more strongly laterally compressed. The anterolateral process is present (Fig. 4n, alp), and the olecranon process seems absent or poorly developed, as in Scutellosaurus9 and Scelidosaurus39. The ischia are poorly preserved (Fig. 4s). The pubic peduncle is separated from the iliac articulation, unlike the continuous cup-shaped structure of most ankylosaurs29. The shaft of the ischium is straight and parallel-edged, as in Scutellosaurus9 and Scelidosaurus39, and distally tapers as in stegosaurs28. The preserved femoral pieces (Fig. 4p) resemble those of basal ornithischians38,39. The bases of both the broken anterior and fourth trochanters (Fig. 4p, at, ft) are large, suggesting large elements; the fourth trochanter is proximally placed on the femoral shaft (near the height of the base of the anterior trochanter); and the distal end of the femur is slightly curved posteriorly. The proximal end of the right fibula (Fig. 4q) is much larger than that of all other thyreophorans (compared with both the femoral and tibial distal ends) and bears a large anterior curved crest. The block-like non-ungual phalanges and a bluntly pointed hoof-like ungual (Fig. 4o, ph, uph) are similar to those of Scelidosaurus39.
At least five osteoderm types are preserved in the holotype of Jakapil. The cervical elements are composed of an external, low-crested scute (Fig. 4t, sc) over a fused, smooth bone base (Fig. 4t, bb), as in Scelidosaurus48 and several ankylosaurs2,49. A probable cervical element is also composed of a concave base of smooth bone fused to a high, asymmetrical osteoderm (Fig. 4t, aco). The bases of these dermal elements present strong rugosities at one edge, suggesting a sutural contact between (Fig. 4t, rug), as in Scelidosaurus48 and some ankylosaurs (such as Pinacosaurus and Scolosaurus40,49,50). Scute-like post-cervical osteoderms (Fig. 4u) are strongly flattened, disk-shaped, and suboval with a very low crest, resembling those of few ankylosaurs such as Gastonia and Gargoyleosaurus51 (‘body osteoderms’ sensu Kinneer et al.52; see also49). Only one scute shows a high triangular cross-section like those of Scelidosaurus48. Also present are a few conical, spike-like osteoderms with deep concave bases (Fig. 4v), and many flat, disk-shaped, minute (7–10 mm) ossicles without crests (Fig. 4w).
The phylogenetic analysis using the matrix of Soto-Acuña et al.5 recovers Jakapil within Thyreophora, as the sister taxon of Ankylosauria (Fig. 5). The branch support for the basal thyreophorans is considerably lower than that obtained by Soto-Acuña et al.5, although the support of Stegosauria and some less inclusive eurypodan clades is slightly better (ceratopsians and pachycephalosaurs also show a lower support). The Jakapil autapomorphies in this analysis are: ventrally orientated basipterygoid processes (char. 134; shared with Agilisaurus, Hypsilophodon, Zalmoxes, Tenontosaurus, Dryosaurus, Liaoceratops, Yamaceratops, Leptoceratops, Bagaceratops and Protoceratops); lateral orientation of the basipterygoid process articular facet (char. 136; shared with Homalocephale, Prenocephale, Stegoceras and Yinlong); a straight dentary tooth row in lateral view (char. 166; shared with the ornithischians Lesothosaurus, Eocursor, Scutellosaurus, Pinacosaurus, Euoplocephalus, heterodontosaurids and neornithischians); the presence of a ventral flange on the dentary (char. 170; shared with Psittacosaurus, Yamaceratops and Protoceratops); a well-developed coronoid process (char. 174; shared with heterodontosaurids and neornithischians); a surangular length of more than 50% the mandibular length (char. 183; shared with Stegoceras, Psittacosaurus, Yinlong, Chaoyangsaurus and Hualianceratops); less than 15 dentary teeth (char. 204; shared with heterodontosaurids, Gasparinisaura, Hypsilophodon, Wannanosaurus, Tenontosaurus, Dryosaurus and ceratopsians); apicobasally tall and blade-like cheek teeth crowns (char. 205; shared with Laquintasaura, Psittacosaurus, Yinlong, Chaoyangsaurus and Hualianceratops). Alternative phylogenetic analyses using the data matrices of Maidment et al.4, Norman6 and Wiersma and Irmis8 recover Jakapil as the sister taxon of Eurypoda (Stegosauria + Ankylosauria) and as a basal ankylosaur, respectively (see Supplementary Information). Being recovered either as an ankylosauromorph or a stem-eurypodan, Jakapil is closely related to Scelidosaurus in all analyses. Detailed phylogenetic results and discussion are provided in the Supplementary Information.
A novel thyreophoran anatomy
The discovery of Jakapil in the Cenomanian of Argentina shows a completely new thyreophoran lineage for the Southern Hemisphere. The new taxon shares many features with basal ornithischians and thyreophorans (even with ankylosaurids, see Supplementary Information), but also bears several novelties. The relatively short mandible of Jakapil (Fig. 2a–d), with a large adductor fossa, extensively ornamented surangular, and a well-developed coronoid eminence (even higher than that of Scelidosaurus), resembles that of heterodontosaurids33 and basal ceratopsians34, suggesting a quite strong bite for a thyreophoran36,53. The wear facets of Jakapil (Fig. 3, dwf, mwf) indicate dental occlusion; they are larger than those of most basal thyreophorans and stegosaurs, resembling those of the adult lectotype of Scelidosaurus10, ankylosaurs, ceratopsids and hadrosaurids36,54. Scelidosaurus shows a patched arrangement of wear along the tooth rows10. In Jakapil, the wear on functional cheek teeth is large and high angled, and seems largely distributed along the tooth rows, from the anteriormost teeth backward, as in heterodontosaurids and cerapodans33,54. On the whole, it is probable that Jakapil had a masticatory system that was more efficient than the early thyreophorans in processing vegetation. The en echelon arrangement of tooth crowns suggests a mainly orthal motion for chewing, as in most thyreophorans6,36,53 (and references therein). In Scelidosaurus and other thyreophorans, the ventrally curved tooth row allows a ‘scissor’ effect of the anteriormost teeth10. By contrast, the straight, narrow snout of Jakapil suggests a different feeding strategy, not cutting leaves but selecting elements that require harder processing36. Thus, Jakapil expands the record of herbivorous vertebrates from the Kokorkom paleodesert, complementing this trophic level that contains the lepidosaur Priosphenodon20.
The predentary bone is the first known for a basal thyreophoran. Despite the variably complete lower jaws in Scutellosaurus9, Emausaurus42, Scelidosaurus10, “Tatisaurus”55 and “Bienosaurus”56, a predentary bone is absent. Norman10 suggested that this may be cartilaginous in Scelidosaurus. The presence of an ossified predentary bone in Jakapil contrasts with that hypothesis. Its plesiomorphic morphology mainly resembles that of the basal ornithischian Lesothosaurus31. It also shows some similarities with the predentary of stegosaurs35 and is very unlike the broad predentary of ankylosaurs29, suggesting a more selective food strategy36. Several features of the predentary, such as the large ventral process, are shared with some basal ceratopsians34. However, this process is usually very robust and proportionally larger that the lateral processes in basal ceratopsians when comparing with Jakapil.
The presence of a dorsomedial process in the articular (Fig. 2c,d,g, dmp) is a new component in a thyreophoran jaw. Some ankylosaurids bear a medial shelf of the glenoid formed by a medial expansion of the articular36. In Jakapil, the glenoid fossa is not medially extended, and the pointed dorsomedial process arises from the retroarticular process. A rather similar process is present in various coelurosaurian theropods, such as dromaeosaurids57, Tyrannosaurus58, Gobipteryx, and ornithurine birds59. In Neornithes, the dorsomedial process of the articular is more anteriorly placed, medial to the mandibular articulation (F. J. R., pers. obs. based on specimens in the Fundación Azara collection: Bubo, Guira, Pterocnemia and Eudromia; see also60), and receives the pterygoid adductor musculature61. In living crocodilians and lepidosaurs, the pterygoid musculature is usually attached to the posteroventral edge of the mandible (also inferred for non-avian dinosaurs61). However, the presence of a medial process in Jakapil may suggest a new placement of the pterygoid musculature, as in birds. If this were the case, the free ventral crest of the mandible (Fig. 2a–d,f, vmc) could have had an exhibition function, rather than being used as an enlarged musculature attachment. In fact, the rugged texture across the mandibular edge resembles an ornamentation element (as in Scelidosaurus10 and Pinacosaurus29; and references therein) with no obvious muscular scar. Otherwise, the crest may represent an enlargement of the surface for musculature insertion, increasing the efficiency of the chewing process (see above).
The armour of Jakapil is also peculiar. Almost all the recovered osteoderms are extremely low, unlike those of basal thyreophorans (Fig. 4r,s,u). The Morphotype A osteoderms of Scutellosaurus62 are very low and bear a central keel, being roughly similar to the disk-shaped osteoderms of Jakapil (Fig. 4s; although the keel of the osteoderms in the latter is smoother). Larger scutes in Jakapil show twice the radial extension of those of Scutellosaurus. Some ankylosaurs, such as Gastonia52 and Gargoyleosaurus51, bear depressed plate-like osteoderms (with or without a low, sharp keel) resembling those of Jakapil. In Scelidosaurus, the osteoderms develop a strong keel48, much higher than that seen in the Jakapil osteoderms. By contrast, large, high-keeled osteoderms and spikes are rare in Jakapil.
The above-mentioned features appear to be novelties, probably due to the poorly known record of thyreophorans in the Southern Hemisphere4,11,12,13,14,15. Moreover, the mixture of plesiomorphic, stegosaurian and ankylosaurian characters of Jakapil may also suggest a basal phylogenetic placement (outside Eurypoda) for this taxon (contra6). In addition, the incorporation of Jakapil into the data matrices of Soto-Acuña et al.5, Norman6, Maidment et al.4, and Wiersma and Irmis8 generates a general decrease in branch support. This demonstrates that the early diversification of thyreophorans is still poorly understood due to their poor Lower-Middle Jurassic fossil record and the scarcity of Gondwanan material4,11, and may explain the ambiguous phylogenetic placement of Jakapil and the early thyreophorans2,4,6.
Bipedalism in armoured dinosaurs
Regarding locomotion, the evolutionary trends observed in thyreophorans are associated with the transition between small, bipedal species and large or graviportal quadrupedal forms, observed in Ankylosauria and Stegosauria1. The transitional state has been attributed to the facultative quadruped Scelidosaurus39. In Jakapil, the relative dimensions of the forelimb, hind limb, and cranial remains (Fig. 4a) bear a greater resemblance to those of the bipedal theropods47, basal ornithischians38 and heterodontosaurids33 than thyreophorans. Moreover, the elongated, non-expanded scapular blade and the strong reduction in the humeri resemble those of specific theropod clades (e.g., abelisaurids47), and unlike the shorter, distally expanded scapular blade of the fully quadrupedal ornithischians and sauropods.
A comparison of the limb elements of some thyreophorans (Suppl. Fig. 4) shows the strong reduction in size of the humerus in Jakapil. Considering a reconstruction of the elements based on Scelidosaurus (the nearest taxon to Jakapil in all phylogenetic analyses), Scutellosaurus (a basal form) and Jinyunpelta (an ankylosaur), the reduction in size is evident. Despite the incompleteness of the material, we quantified this reduction comparing the proximal humeral (PHW) and the distal femoral widths (DFW; the distal end of the femur in Jakapil was measured in the only well-preserved transversal section, although this is not the most distal). The proximal humeral width/distal femoral width ratio (HFR) is lower in the basal taxa (Jakapil, Scutellosaurus and Scelidosaurus) with respect to the ankylosaurs Jinyunpelta and Euoplocephalus, showing a widening of the humerus in the quadrupedal taxa reaching a comparable width (ratio ~ 1). Such widening in the proximal humeral end is evident in the lack of fit of the Jakapil bones in the Jinyunpelta proportions, also suggesting limb proportions more similar to those of basal forms. Moreover, the incomplete distal end of the femur in Jakapil allows even smaller values of the HFR ratio (and of the humerus size). Also, a shortening of the humerus relative to the femur is present in the obligate quadrupedal Ankylosauria. Regardless of the unknown humeral length, the lack of a robust humerus in Jakapil allows us to reject a fully quadrupedal stance like that of the heavily built ankylosaurs.
In summary, the overall limb dimensions and estimations (with forelimb and olecranon process both reduced63), and the femoral anatomical similarities to the basal ornithischians and thyreophorans39 (e.g., large trochanters and a non-columnar element) suggest a bipedal stance in the specimen. However, the incompleteness of the remains demands caution to define the stance of Jakapil. To make more complex the scenery, Jakapil still retains quadruped-associated features, such as a probable anterolateral process in the ulna, and stout metacarpals63 (and references therein). More complete material is needed to make accurate quantitative comparisons with other taxa and clarify its stance.
Paleobiogeography of early thyreophorans
The Early Jurassic thyreophoran record consists of basal forms known from several continents showing a Pangean distribution. These comprise Scutellosaurus (Hettangian-Toarcian of the USA9), Scelidosaurus (Sinemurian of the UK; see 6,10), Emausaurus (Toarcian of Germany42), ‘Lusitanosaurus’ (Sinemurian of Portugal1), ‘Bienosaurus’, ‘Tatisaurus’ (both from the Hettangian-Sinemurian of China; see55,56) and Yuxisaurus (late Sinemurian-Toarcian64). Some recent papers recover the unarmoured ornithischians Lesothosaurus (Hettangian-Sinemurian of South Africa and Lesotho; see3,31) and Laquintasaura (Hettangian of Venezuela; see3,4,65) as Gondwanan basal members of Thyreophora. However, alternative studies show their phylogenetic position as controversial3,6,65, so they cannot be confidently assigned to Thyreophora.
The extensive distribution of armoured basal thyreophorans (excluding both Lesothosaurus and Laquintasaura) across the northern landmasses during the Early Jurassic shows a rapid diversification after the origin of the clade. However, basal thyreophoran remains from Gondwana known from the Middle Jurassic of Niger66, along with problematic material from the Lower Jurassic (Sinemurian-Pliensbachian) of India (see55,67 and references therein), suggest a more extensive distribution for the early thyreophorans. In addition, the early distribution of stegosaurs and ankylosaurs shows a similar pattern. The presence of the Middle Jurassic basal stegosaur Isaberrysaura from the Bajocian of Argentina68,4 and the stegosaurid Adratiklit from the Bathonian-Callovian of Morocco4 depict a distribution of the early stegosaurs that extends into southern landmasses. The Middle Jurassic thyreophoran fossil record also includes the stegosaur Loricatosaurus from the Callovian of England and France, the ankylosaurs Sarcolestes and ‘Cryptosaurus’ from the Callovian of England, the ankylosaur Spicomellus from the Bathonian-Callovian of Morocco15, the ankylosaur ‘Tianchisaurus’ from the Callovian of China, and indeterminate remains from Europe and Asia (see4,67 and references therein). On the whole, the Pangean distribution of early thyreophorans across the Early-Middle Jurassic makes it difficult to recognize a source area for Thyreophora and the most inclusive clades within it.
In this context, Jakapil not only increases the poor Gondwanan record of thyreophorans, but also establishes a theoretical framework for Gondwanan basal thyreophoran evolution and distribution (Fig. 5). Whether Jakapil is recovered as an ankylosaur or a non-eurypodan thyreophoran, it is closely related to Scelidosaurus (see Supplementary Information). The presence of a basal thyreophoran in the early Late Cretaceous of South America shows that an ancient Gondwanan lineage of early thyreophorans evolved independently from those of the Northern Hemisphere, whose relationships have to be traced during the Early-Middle Jurassic Pangean rupture and the consequent isolation of Gondwana and later South America. Accordingly, early Gondwanan thyreophorans survived a long time after the Pangean breakup, whereas the northern early thyreophorans seem to have gone extinct by the Middle Jurassic. The persistence of a Gondwanan lineage of thyreophorans finds support in new thyreophoran remains recovered from the Lower Cretaceous rocks of the Bajada Colorada Formation (Berriasian-Hauterivian), also from the Argentinian Patagonia (Neuquén Province). These remains are composed of a diversity of osteoderms, showing either a mixture of thyreophorans at the site, or a new, still poorly understood lineage69.
A new lineage of Gondwanan thyreophorans was recently proposed by Soto-Acuña et al.5, Parankylosauria. This clade includes Antarctopelta (Campanian-Maastrichthian of Antarctica), Stegouros (Campanian-Maastrichthian of South America), and the traditionally basal ankylosaur Kunbarrasaurus (Albian-Cenomanian of Australia)5. Despite their extensive Gondwanan distribution during the Cretaceous, anatomical differences with Jakapil are remarkable. Parankylosaurs show ankylosaurian features, like broad ornamented skulls, depressed caudal vertebrae, similar limb proportions, and a columnar femur with both reduced anterior and fourth trochanters (among others), which contrast with the mixture of features of Jakapil. Even more, ankylosaurian features present in Jakapil were recognized as convergent with ankylosaurids within Euankylosauria (e.g., a straight dentary tooth row in lateral view, a small diastema on the dentary, a shallow symphysis, scapular blade shape; see Supplementary Information) rather than with parankylosaurs. Therefore, a close phylogenetic relation between them is unlikely. Until more records contribute to the understanding of Gondwanan thyreophorans, both Jakapil and parankylosaurs belong to two different lineages. This shows that Gondwanan thyreophorans were a diverse clade with morphologically disparity.
On the other hand, further work will help to fill the extensive gap between the early thyreophorans and the Cretaceous remains from South America. Recent research is reflected in an increase in the thyreophoran fossil record from South America, with all its implications for thyreophoran evolution11,12,13,14,69,70; and this paper). The discovery of Jakapil not only supports the presence of a new Gondwanan lineage of early thyreophoran dinosaurs that persisted in Gondwana for a long time, but has also brought to light the importance of the Gondwanan fossil record in the study of the origin and evolution of dinosaurs (and other clades).
We used the dataset of Soto-Acuña et al.5, that comprises a broad sample of ornithischians suitable to test the phylogenetic position of Jakapil, a specimen with a complex mixture of features complete enough to include both several outgroups (non-thyreophoran ornithischians) and also both groups of thyreophorans. The dataset consists of 75 taxa and 383 morphological characters (see character list in Soto-Acuña et al.5 and references therein). Marasuchus was fixed as the outermost outgroup taxon. All characters were unweighted. Characters 2, 23, 31, 39, 125, 163, 196, 203, 204, 222, 227, 238, 243, 247, 268, 292, 296, 302, 306, 320 and 361 were treated as additive. Memory space was made for 1,500,000 trees.
Phylogenetic analyses of the morphological matrix were carried out in TNT v1.5 (see Supplementary Information). A Traditional search was applied with 10,000 replicates of Wagner trees under the tree bisection reconnection (TBR) algorithm, saving 10 trees per replication. Trees saved in memory were resampled with an additional round of TBR. The support for each node in the trees was assessed in TNT. Bremer values were also recorded with Traditional searches until 22 suboptimal trees. Bootstrap analysis was carried out using 10,000 pseudoreplicates with a Traditional search, and Absolute frequencies. Consistency and retention indexes (from the archive STATS.RUN), character mapping, and moving taxon positions over the consensus to test parsimony, were carried out in TNT. The detailed phylogenetic methods are provided in the Supplementary Information.
Norman, D. B., Witmer, L. M. & Weishampel, D. B. Basal Thyreophora. In The Dinosauria 2nd edn (eds Weishampel, D. B. et al.) 335–342 (University of California Press, 2004).
Arbour, V. M. & Currie, P. J. Systematics, phylogeny and palaeobiogeography of the ankylosaurid dinosaurs. J. Syst. Palaeontol. 14, 385–444. https://doi.org/10.1080/14772019.2015.1059985 (2016).
Baron, M. G., Norman, D. B. & Barrett, P. M. Postcranial anatomy of Lesothosaurus diagnosticus (Dinosauria: Ornithischia) from the Lower Jurassic of southern Africa: Implications for basal ornithischian taxonomy and systematics. Zool. J. Linn. Soc. 179, 125–168. https://doi.org/10.1111/zoj.12434 (2017).
Maidment, S. C. R., Raven, T. J., Ouarhache, D. & Barrett, P. M. North Africa’s first stegosaur: Implications for Gondwanan thyreophoran dinosaur diversity. Gondwana Res. 77, 82–97. https://doi.org/10.1016/j.gr.2019.07.007 (2020).
Soto-Acuña, S. et al. Bizarre tail weaponry in a transitional ankylosaur from subantarctic Chile. Nature. https://doi.org/10.1038/s41586-021-04147-1 (2021).
Norman, D. B. Scelidosaurus harrisonii Owen, 1861 (Dinosauria: Ornithischia) from the Early Jurassic of Dorset, England: Biology and phylogenetic relationships. Zool. J. Linn. Soc. 191, 1–86. https://doi.org/10.1093/zoolinnean/zlaa061 (2020).
Carpenter, K. Phylogenetic analysis of the Ankylosauria. In The Armored Dinosaurs (ed. Carpenter, K.) 455–483 (Indiana University Press, 2001).
Wiersma, J. P. & Irmis, R. B. A new southern Laramidian ankylosaurid, Akainacephalus johnsoni gen. et sp. nov., from the Upper Campanian Kaiparowits formation of southern Utah. PeerJ 6, e5016. https://doi.org/10.7717/peerj.5016 (2018).
Breeden, B. T., Raven, T. J., Butler, R. J., Rowe, T. B. & Maidment, S. C. R. The anatomy and palaeobiology of the early armoured dinosaur Scutellosaurus lawleri (Ornithischia: Thyreophora) from the Kayenta Formation (Lower Jurassic) of Arizona. R. Soc. Op. Sci. 8, 201676. https://doi.org/10.1098/rsos.201676 (2021).
Norman, D. B. Scelidosaurus harrisonii Owen, 1861 (Dinosauria: Ornithischia) from the Early Jurassic of Dorset, England: Cranial anatomy. Zool. J. Linn. Soc. 188, 1–81. https://doi.org/10.1093/zoolinnean/zlz074 (2020).
Pereda-Suberbiola, X., Díaz-Martínez, I., Salgado, L. & De Valais, S. Síntesis del registro fósil de dinosaurios tireóforos en Gondwana. In: M. Fernández y Y. Herrera (Eds.) Reptiles Extintos—Volumen en Homenaje a Zulma Gasparini. Publ. Electr. Asoc. Paleontol. Arg. 15(1), 90–107. https://doi.org/10.5710/PEAPA.21.07.2015.101 (2015).
Leahey, L. G., Molnar, R. E., Carpenter, K., Witmer, L. M. & Salisbury, S. W. Cranial osteology of the ankylosaurian dinosaur formerly known as Minmi sp. (Ornithischia: Thyreophora) from the Lower Cretaceous Allaru Mudstone of Richmond, Queensland, Australia. PeerJ 3, e1475l. https://doi.org/10.7717/peerj.1475 (2015).
Murray, A., Riguetti, F. & Rozadilla, S. New ankylosaur (Thyreophora, ornithischia) remains from the Upper Cretaceous of Patagonia. J. S. Am. Earth Sci. 96, 102320. https://doi.org/10.1016/j.jsames.2019.102320 (2019).
Rauhut, O. W. M., Carballido, J. L. & Pol, D. First osteological record of a Stegosaur (Dinosauria, Ornithischia) from the Upper Jurassic of South America. J. Vert. Paleontol. 40, e1862133. https://doi.org/10.1080/02724634.2020.1862133 (2020).
Maidment, S. C. R. et al. Bizarre dermal armour suggests the first African ankylosaur. Nat. Ecol. Evol. https://doi.org/10.1038/s41559-021-01553-6 (2021).
CandiaHalupczok, D. J., Sánchez, M. L., Veiga, G. D. & Apesteguía, S. Dinosaur tracks in the Kokorkom Desert, Candeleros Formation (Cenomanian, Upper Cretaceous), Patagonia Argentina: Implications for deformation structures in dune fields. Cret. Res. 83, 194–206. https://doi.org/10.1016/j.cretres.2017.10.017 (2018).
Pérez-Mayoral, J., Argüello Scotti, A., Apesteguía, S. & Veiga, G. D. High-resolution analysis of an erg-margin system from the Cretaceous Candeleros Formation (La Buitrera Paleontological Area, Río Negro Province, Argentina): An approach to different scales of fluvial-aeolian interactions. Lat. Am. J. Sedim. Basin Anal. 28(1), 37–59 (2021).
Makovicky, P. J., Apesteguía, S. & Agnolín, F. L. The earliest dromaeosaurid theropod from South America. Nature 437, 1007–1011. https://doi.org/10.1038/nature03996 (2005).
Fernández Dumont, M. L., Bona, P., Pol, D. & Apesteguía, S. New anatomical information on Araripesuchus buitreraensis with implications for the systematics of Uruguaysuchidae (Crocodyliforms, Notosuchia). Cret. Res. 113, 104494. https://doi.org/10.1016/j.cretres.2020.104494 (2020).
Apesteguía, S. & Novas, F. E. Large Cretaceous sphenodontian from Patagonia provides insight into lepidosaur evolution in Gondwana. Nature 425, 609–612. https://doi.org/10.1038/nature01995 (2003).
Garberoglio, F. F. et al. New skulls and skeletons of the Cretaceous legged snake Najash, and the evolution of the modern snake body plan. Sci. Adv. 5, 5833. https://doi.org/10.1126/sciadv.aax5833 (2019).
Apesteguía, S., Agnolín, F. L. & Lio, G. L. An early Late Cretaceous lizard from Patagonia, Argentina. C. R. Palevol. 4(4), 311–315. https://doi.org/10.1016/j.crpv.2005.03.003 (2005).
Maniel, I. J. et al. Cranial and postcranial remains of a new species of Prochelidella (Testudines: Pleurodira: Chelidae) from ‘La Buitrera’ (Cenomanian of Patagonia, Argentina), with comments on the monophyly of this extinct chelid genus from southern Gondwana. J. Syst. Palaeontol. 20(12), 1033–1055. https://doi.org/10.1080/14772019.2020.1721579 (2020).
Rougier, G. W., Apesteguía, S. & Gaetano, L. C. Highly specialized mammalian skulls from the Late Cretaceous of South America. Nature 479, 97–102. https://doi.org/10.1038/nature10591 (2011).
Owen, R. Report on British fossil reptiles. Part 2. Rep. Brit. Assoc. Adv. Sci. (Plymouth) 11, 60–204 (1842).
Seeley, H. G. On the classification of the fossil animals commonly named Dinosauria. Proc. R. Soc. Lond. 43, 165–171 (1887 ).
Nopcsa, F. Die Dinosaurier des siebenbürgischen Landesteile Ungarns. Mitt. Jahrb. Ungar. Geol. Reichsanst. Budapest 23, 3–24 (1915).
Galton, P. M. & Upchurch, P. Stegosauria. In The Dinosauria 2nd edn (eds Weishampel, D. B. et al.) 343–362 (University of California Press, 2004).
Vickaryous, M. K., Maryańska, T. & Weishampel, D. B. Ankylosauria. In The Dinosauria 2nd edn (eds Weishampel, D. B. et al.) 363–392 (University of California Press, 2004).
Butler, R. J., Upchurch, P. & Norman, D. B. The phylogeny of the ornithischian dinosaurs. J. Syst. Palaeontol. 6, 1–40. https://doi.org/10.1017/S1477201907002271 (2008).
Porro, L. B., Witmer, L. M. & Barrett, P. M. Digital preparation and osteology of the skull of Lesothosaurus diagnosticus (Ornithischia: Dinosauria). PeerJ 3, e1494. https://doi.org/10.7717/peerj.1494 (2015).
Boyd, C. A. The cranial anatomy of the neornithischian dinosaur Thescelosaurus neglectus. PeerJ 2, e669. https://doi.org/10.7717/peerj.669 (2014).
Sereno, P. C. Taxonomy, morphology, masticatory function and phylogeny of heterodontosaurid dinosaurs. ZooKeys 226, 1–225. https://doi.org/10.3897/zookeys.226.2840 (2012).
You, H.-L. & Dodson, P. Basal Ceratopsia. In The Dinosauria 2nd edn (eds Weishampel, D. B. et al.) 478–493 (University of California Press, 2004).
Sereno, P. C. & Dong, Z. The skull of the basal stegosaur Huayangosaurus taibaii. J. Vert. Paleontol. 11, 318–343. https://doi.org/10.1080/02724634.1992.10011463 (1992).
Ősi, A., Prondvai, E., Mallon, J. & Bodor, E. R. Diversity and convergences in the evolution of feeding adaptations in ankylosaurs (Dinosauria: Ornithischia). Hist. Biol. 29, 539–570. https://doi.org/10.1080/08912963.2016.1208194 (2016).
Boyd, C. A. The systematic relationships and biogeographic history of ornithischian dinosaurs. PeerJ 3, e1523. https://doi.org/10.7717/peerj.1523 (2015).
Norman, D. B., Witmer, L. M. & Weishampel, D. B. Basal ornithischians. In The Dinosauria 2nd edn (eds Weishampel, D. B. et al.) 325–334 (University of California Press, 2004).
Norman, D. B. Scelidosaurus harrisonii Owen, 1861 (Dinosauria: Ornithischia) from the Early Jurassic of Dorset, England: Postcranial endoskeleton. Zool. J. Linn. Soc. 189, 47–157. https://doi.org/10.1093/zoolinnean/zlz078 (2020).
Arbour, V. M. & Currie, P. J. Euoplocephalus tutus and the diversity of ankylosaurid dinosaurs in the Late Cretaceous of Alberta, Canada, and Montana, USA. PLoS ONE 8, e62421. https://doi.org/10.1371/journal.pone.0062421 (2013).
Blows, W. T. British Polacanthid Dinosaurs—Observations on the History and Palaeontology of the UK Polacanthid Armoured Dinosaurs and Their Relatives 220 (Siri Scientific Press, 2015).
Haubold, H. Ein neuer Dinosaurier (Ornithischia, Thyreophora) aus dem unteren Jura des nördlichen Mitteleuropa. Rev. Paléobiol. 9, 149–177 (1990).
Zhou, S. The Middle Jurassic Dinosaurian fauna from Dashanpu, Zigong, Sichuan, Vol. 2 (Stegosaurs). Chengdu. Sich. Sci. Tech. Publ. House. 2, 52 (1984).
Maidment, S. C. R., Wei, S. & Norman, D. B. Re-description of the postcranial skeleton of the Middle Jurassic stegosaur Huayangosaurus taibaii. J. Vert. Paleontol. 26, 944–956. https://doi.org/10.1671/0272-4634(2006)26[944:ROTPSO]2.0.CO;2 (2006).
Park, J.-Y. et al. A new ankylosaurid skeleton from the Upper Cretaceous Baruungoyot Formation of Mongolia: Its implications for ankylosaurid postcranial evolution. Sci. Rep. 11, 4101. https://doi.org/10.1038/s41598-021-83568-4 (2021).
Brown, C. M., Boyd, C. A. & Russell, A. P. A new basal ornithopod dinosaur (Frenchman Formation, Saskatchewan, Canada), and implications for late Maastrichtian ornithischian diversity in North America. Zool. J. Linn. Soc. 163, 1157–1198. https://doi.org/10.1111/j.1096-3642.2011.00735.x (2011).
Burch, S. H. Osteological, myological, and phylogenetic trends of forelimb reduction in nonavian theropod dinosaurs. PhD Dissertation. Stony Brook University (2013).
Norman, D. B. Scelidosaurus harrisonii Owen, 1861 (Dinosauria: Ornithischia) from the Early Jurassic of Dorset, England: Dermal skeleton. Zool. J. Linn. Soc. 190, 1–53. https://doi.org/10.1093/zoolinnean/zlz085 (2020).
Ford, T. L. A review of ankylosaur osteoderms from New Mexico and a preliminary review of ankylosaur armor. New Mex. Mus. Nat. Hist. Sci. Bull. 17, 157176 (2000).
Burns, M. E., Tumanova, T. A. & Currie, P. J. Postcrania of juvenile Pinacosaurus grangeri (Ornithischia: Ankylosauria) from the upper Cretaceous Alagteeg Formation, Alag Teeg, Mongolia: Implications for ontogenetic allometry in ankylosaurs. J. Paleontol. 89, 168–182. https://doi.org/10.1017/jpa.2014.14 (2015).
Kilbourne, B. & Carpenter, K. Redescription of Gargoyleosaurus parkpinorum, a polacanthid ankylosaur from the Upper Jurassic of Albany County, Wyoming. Neu. Jahrb. Geol. Paläontol. Abhandlungen. 237, 111–160. https://doi.org/10.1127/njgpa/235/2005/111 (2005).
Kinneer, B., Carpenter, K. & Shaw, A. Redescription of Gastonia burgei (dinosauria: Ankylosauria, Polacanthidae), and description of a new species. Neues Jahrb. Geol. Paläontol. Abh. 282, 37–80. https://doi.org/10.1127/njgpa/2016/0605 (2016).
Barrett, P. M. Tooth wear and possible jaw action of Scelidosaurus harrisonii Owen and a review of feeding mechanisms in other thyreophoran dinosaurs. In The Armored Dinosaurs (ed. Carpenter, K.) 25–52 (Indiana University Press, 2001).
Mallon, J. C. & Anderson, J. S. The functional and palaeoecological implications of tooth morphology and wear for the megaherbivorous dinosaurs from the Dinosaur Park Formation (Upper Campanian) of Alberta, Canada. PLoS ONE 9(6), e98605. https://doi.org/10.1371/journal.pone.0098605 (2014).
Norman, D. B., Butler, R. J. & Maidment, S. C. R. Reconsidering the status and affinities of the ornithischian dinosaur Tatisaurus oehleri Simmons, 1965. Zool. J. Linn. Soc. 150, 865–874. https://doi.org/10.1111/J.1096-3642.2007.00301.X (2007).
Raven, T. J., Barrett, P. M. & Maidment, S. C. R. A reassessment of the purported ankylosaurian dinosaur Bienosaurus lufengensis from the Lower Lufeng of Yunnan, China. Acta Palaeontol. Pol. 64, 335–342. https://doi.org/10.4202/app.00577.2018 (2019).
Norell, M. A. et al. A new dromaeosaurid theropod from Ukhaa Tolgod (Ömnögov, Mongolia). Am. Mus. Novit. 3545, 1–51. https://doi.org/10.1206/0003-0082(2006)3545[1:ANDTFU]2.0.CO;2 (2006).
Brochu, C. A. Osteology of Tyrannosaurus rex: Insights from a nearly complete skeleton and high-resolution computed tomographical analysis of the skull. J. Vert. Paleontol. 22(4), 1–138. https://doi.org/10.1080/02724634.2003.10010947 (2003).
Elzanowski, A. A comparison of the jaw skeleton in theropods and birds, with a description of the palate in the Oviraptoridae. In: Olson SL (ed) Avian Paleontology at the close of the 20th century: Proceedings of the 4th International meeting of the Society for Avian Paleontology and Evolution, Washington, D.C., 4–7 June 1996. Smith. Contrib. Paleobiol. 89, 311–323 (1999).
Mayr, G. Cenozoic mystery birds—On the phylogenetic affinities of bony-toothed birds (Pelagornithidae). Zool. Scr. 40, 448–467. https://doi.org/10.1111/j.1463-6409.2011.00484.x (2011).
Holliday, C. M. & Witmer, L. M. Archosaur adductor chamber evolution: integration of musculoskeletal and topological criteria in jaw muscle homology. J. Morphol. 268, 457–484. https://doi.org/10.1002/jmor.10524 (2007).
Breeden, B. T. III. & Rowe, T. B. New specimens of Scutellosaurus lawleri Colbert, 1981, from the Lower Jurassic Kayenta Formation in Arizona elucidate the early evolution of thyreophoran dinosaurs. J. Vert. Paleontol. 40, e1791894. https://doi.org/10.1080/02724634.2020.1791894 (2020).
Maidment, S. C. R. & Barrett, P. M. Osteological correlates for quadrupedality in ornithischian dinosaurs. Acta Palaeontol. Pol. 59(1), 53–70. https://doi.org/10.4202/app.2012.0065 (2014).
Yao, X., Barrett, P. M., Yang, L., Xu, X. & Bi, S. A new early branching armored dinosaur from the Lower Jurassic of southwestern China. Elife 11, e75248. https://doi.org/10.7554/eLife.75248 (2022).
Barrett, P. M. et al. A palaeoequatorial ornithischian and new constraints on early dinosaur diversification. Proc. R. Soc. B 281, 20141147. https://doi.org/10.1098/rspb.2014.1147 (2014).
Ridgwell, N. & Sereno, P. C. A basal thyreophoran (Dinosauria, Ornithischia) from the Tiouraren Formation of Niger. J. Vert. Paleontol. 30(2), 150A–151A (2010).
Galton, P. M. Earliest record of an ankylosaurian dinosaur (Ornithischia: Thyreophora): dermal armor from the lower Kota Formation (Lower Jurassic) of India. Neues Jahrb. Geol. Paläontol. Abh. 291, 205–219. https://doi.org/10.1127/njgpa/2019/0800 (2019).
Salgado, L. et al. A new primitive neornithischian dinosaur from the Jurassic of Patagonia with gut contents. Sci. Rep. 7, 42778. https://doi.org/10.1038/srep42778 (2017).
Riguetti, F., Gallina, P., Apesteguía, S. & Canale, J. I. New thyreophoran (Dinosauria, Ornithischia) remains from the lower Cretaceous Bajada Colorada Formation (Neuquén, Argentina). Reunión de Comunicaciones de la Asociación Paleontológica Argentina, 2019. Publ. Electr. Assoc. Paleontol. Arg. 20(1), R49 (2020).
Rozadilla, S., Agnolín, F., Manabe, M., Tsuihiji, T. & Novas, F. E. Ornithischian remains from the Chorrillo Formation (Upper Cretaceous), southern Patagonia, Argentina, and their implications on ornithischian paleobiogeography in the Southern Hemisphere. Cret. Res. 125, 104881. https://doi.org/10.1016/j.cretres.2021.104881 (2021).
The authors thank to Mariluan family for kindly allowing us the access to the fossiliferous locality of Cerro Policía and to the Secretaría de Cultura of the Río Negro Province for allowing the respective permits; to the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación (projects PICT 2014-0564 and PICT 2018-04598), the Fundación Azara-Universidad Maimónides, the Spanish Ministerio de Ciencia, Innovación e Universidades and the European Regional Development Fund (projects CGL2017-85038-P and PID2021-122612OB-I00), and the Gobierno Vasco/EJ (research group IT1418-19) for the funding. F. J. R. thanks to I. Díaz-Martínez, A. Martinelli, L. Leahey, R. Molnar, A. Vargas Milne, S. Soto Acuña, and M. Baron for digital material; to L. Pazo and J. Kaluza for the material preparation; to the members of the Area de Paleontología of the Fundación Azara, especially F. Garberoglio, L. Fernández Dumont and J. P. Garderes, for all the helping; to R. Ponti for the thin sectioning, and I. Cerda for his advice on histological aspects; to S. Bogan, S. M. Álvarez and J. Meluso for facilitate the access to the Fundación Azara collections. S. A. acknowledges J. Kaluza for identifying key materials. Thanks to R. Glasgow for reviewing the English text of the manuscript. Special thanks to the reviewers Susannah Maidment, Victoria Arbour, and an anonymous reviewer, whose comments strongly improved the manuscript.
The authors declare no competing interests.
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Cite this article
Riguetti, F.J., Apesteguía, S. & Pereda-Suberbiola, X. A new Cretaceous thyreophoran from Patagonia supports a South American lineage of armoured dinosaurs.
Sci Rep 12, 11621 (2022). https://doi.org/10.1038/s41598-022-15535-6
Received: 04 December 2021
Accepted: 24 June 2022
Published: 11 August 2022
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