Marine ecosystem recovery after the Permo-Triassic mass extinction (PTME) has been extensively studied in the shallow sea, but little is known about the nature of this process in pelagic ecosystems. Omphalosauridae, an enigmatic clade of open-water durophagous marine reptiles, potentially played an important role in the recovery, but their fragmentary fossils and uncertain phylogenetic position have hindered our understanding of their role in the process. Here we report the large basal ichthyosauriform Sclerocormus from the Early Triassic of China that clearly demonstrates an omphalosaurid affinity, allowing for the synonymy of the recently erected Nasorostra with Omphalosauridae. The skull also reveals the anatomy of the unique feeding apparatus of omphalosaurids, likely an adaptation for feeding on hard-shelled pelagic invertebrates, especially ammonoids. Morphofunctional analysis of jaws shows that omphalosaurids occupy the morphospace of marine turtles. Our discovery adds another piece of evidence for an explosive radiation of marine reptiles into the ocean in the Early Triassic and the rapid recovery of pelagic ecosystems after the PTME.
Marine ecosystem recovery after the Permo-Triassic mass extinction (PTME), the most severe extinction in the history of the Earth, has been traditionally regarded as delayed and gradual1,2. However, this view has been challenged by an increasing number of recent discoveries suggesting the rapid emergence and evolution of Mesozoic marine reptiles in the aftermath of the PTME3,4,5,6,7,8. Marine reptiles attained high taxonomic and ecomorphological diversity as early as the late Early Triassic, and included generalist predators9, piscivores10, specialized forms using non-visual prey detection11, lunge feeders6 and durophages12. Durophagy evolved independently in several clades of Triassic marine reptiles, including ichthyosauriforms (the recently erected nasorostrans and several groups of ichthyopterygians)13,14, placodonts15 and thalattosaurs16, but these durophagous ecomorphs were mostly limited to shallow-water environments and likely fed on abundant, sessile and benthic hard-shelled invertebrates. In fact, our understanding of the ecosystem recovery after the PTME is in general heavily biased towards data from shallow-water environments17 and relatively little is known about the nature of the recovery in open-water ecosystems3.
Ammonoids, a now extinct group of open marine cephalopods, had a successful ecological and evolutionary history for >300 million years during the Palaeozoic and Mesozoic, but their evolution experienced a severe bottleneck, with only three genera surviving the PTME18. Immediately after the mass extinction, however, ammonoids diversified explosively in the first few million years, and continued to play a significant ecological role for the rest of the Mesozoic due to their abundance, wide distribution, and high evolutionary rates18. Despite their high abundance in Mesozoic marine ecosystems, little is known about predation on ammonoids19. While sharks, mosasaurs, and cephalopods have been hypothesized as major groups that preyed upon ammonoids in the Jurassic and Cretaceous oceans, information regarding predators on Triassic ammonoids is scanty19.
Omphalosauridae, comprising several species in the genus Omphalosaurus, is an enigmatic group of durophagous marine reptiles known hitherto from Early–Middle Triassic pelagic sediments of Western North America20,21, Svalbard22, and the Bavarian Alps23. There is one exception where a single jaw fragment was found in the Middle Triassic shallow marine carbonates of Southern Poland, but this occurence is likely a stray carcass24. Omphalosaurids are characterised by the presence of durophagous dentition arranged in unique dental batteries both in the upper and lower jaws, in which functional teeth underwent extreme tooth wear leading to almost complete tooth loss before shedding23. Even though omphalosaurids were first reported over a century ago20, they are represented in the fossil record mostly by jaw fragments and only a few specimens preserving partial cranial and postcranial remains have been discovered to date20,23. As a consequence, the taxonomic affinity of omphalosaurids has remained elusive, with several groups of Mesozoic reptiles, including rhynchosaurs, placodonts and ichthyosaurs, proposed as their closest relatives20,21,23. The incomplete nature of omphalosaurid fossil material, as well as some stark anatomical differences between them and other groups of Mesozoic reptiles, have hindered their unambiguous placement in a phylogenetic context and their role in pelagic ecosystem recovery after the PTME.
Here, we describe a new specimen of the basal ichthyosauriform Sclerocormus25 from the Early Triassic of China. Its skull and dentition share numerous synapomorphies with those present in Omphalosaurus and another basal ichthyosauriform – Cartorhynchus13. Our phylogenetic analysis unambiguously establishes omphalosaurids as early diverging ichthyosauriforms and necessitates the synonymy of the recently erected Nasorostra (comprising Sclerocormus and Cartorhynchus) with Omphalosauridae. The skull of the new specimen also reveals the anatomy of the bizarre feeding apparatus of omphalosaurids, suggesting the presence of a grinding mechanism unique among Triassic marine reptiles, that probably evolved as an adaptation for feeding on hard-shelled pelagic invertebrates, especially ammonoids. The peculiar feeding ecology of omphalosaurids likely enabled these reptiles to become geographically widespread rapidly following the PTME event, suggesting the early establishment of complex and functional trophic webs in pelagic waters.
Diapsida Osborn, 1903
Ichthyosauromorpha Motani et al., 2015
Ichthyosauriformes Motani et al., 2015
Omphalosauridae Merriam, 1906 (=Nasorostra Jiang et al., 2016)
The last common ancestor of Omphalosaurus nevadanus, Cartorhynchus lenticarpus and Sclerocormus parviceps and all of its descendants.
Omphalosauridae is differentiated from all other Ichthyosauriformes by the presence of the following synapomorphies: elongate nasal reaching the snout tip; maxilla excluded from the border of the external naris; crushing dentition forming irregular maxillary and dentary batteries concentrated along cranial midline; dome-shaped tooth crown; first maxillary and dentary teeth rounded and blunt; premaxilla edentulous; convex occlusal surface of maxilla and corresponding concave occlusal surface of dentary; deep posterior mandible with slanting end and low jaw joint; wing-like process on posterior dentary.
Sclerocormus Jiang et al., 2016
Skull small; tail long; trunk short and deep; preorbital snout constricted and short; preorbital and postorbital parts of skull subequal in length; postorbital extending backward to the posterior edge of the upper temporal fenestra; parietal posteriorly bifurcating into two prongs; coracoid larger than scapula; humerus and femur straight; radius and ulna subequal in length; gastralia robust and comprising three sets, each gradually tapering towards their lateral ends.
Sclerocormus cf. parviceps Jiang et al., 2016
HFUT MJS-16-012, a partial skeleton housed at Hefei University of Technology (HFUT). The new specimen was collected from Majiashan quarry in Chaohu, Hefei, Anhui Province, China (Fig. 1). The fossiliferous horizon is from the Upper Member of the Nanlinghu Formation, Spathian, Olenekian, Lower Triassic (~248 Ma), representing an open water environment (Supplementary Figs. 1, 2; Supplementary Results). The specimen was largely prepared from ventral view, but the skull was also prepared from both lateral sides as much as possible (Figs. 2, 3). Measurements of HFUT MJS-16-012 are available in Supplementary Results and Supplementary Table 1, respectively. The new information available from HFUT MJS-16-012 also allows us to re-interpret the morphology of Omphalosaurus cf. O. nevadanus (MBG 1500; see Supplementary Fig. 4 and Supplementary Results) - a key specimen of Omphalosaurus23 to compare with the Chinese specimens.
HFUT MJS-16-012 is referred to Sclerocormus on the basis of its large body size compared to the co-occurring Cartorhynchus13, as well as a well-developed gastral basket and ossified centralia that clearly differentiate it from Cartorhynchus13. The skull length of HFUT MJS-16-012 cannot be accurately measured since the tip of the snout is damaged. However, the upper and lower jaws are well articulated with each other in HFUT MJS-16-012 (Figs. 2, 3), and there is no apparent overbite present in the Cartorhynchus holotype13, the only known omphalosaurid specimen with well-preserved and articulated upper and lower jaws. Therefore, we can safely estimate the skull length of HFUT MJS-16-012 by measuring it from the tip of the lower jaw to the posterior margin of the supratemporal. This gives a minimum estimate of the skull length of 226.7 mm for HFUT MJS-16-012 since the tip of the lower jaw is also slightly damaged. Thus, we estimate that the HFUT MJS-16-012 skull is more than twice larger than the skull of the holotype of S. parviceps (skull length = 100 mm)25. Using the simple skull-body length proportion of the holotype specimen, the total length of HFUT MJS-16-012 is estimated to have reached as much as 3.6 m. However, HFUT MJS-16-012 might still not be fully mature as the carpal region is poorly ossified. Whether the stark difference in body size between HFUT MJS-16-012 and the holotype of S. parviceps is due to taxonomic or intraspecific variation remains uncertain. HFUT MJS-16-012 also possesses a proportionally smaller orbit than the holotype specimen (1/4 of skull length, compared with 1/3 for the holotype), a frontal contribution to the orbit (frontal excluded from orbital margin in holotype), three rows of gastralia (two rows of gastral elements reported in holotype), and one centralium and one distal carpal preserved in the forefin (in contrast to two centralia and two distal carpals preserved in the holotype). The decrease in the relative size of the orbit throughout ontogeny has been demonstrated in ichthyopterygians and other reptiles26, so a similar phenomenon in Sclerocormus seems likely. Furthermore, the skull of the holotype specimen is dorsolaterally compressed. This is likely to have an effect on the perceived differences in the relative contributions of the frontals to the orbital margin between both specimens. Because the gastral basket in the holotype specimen is largely disarticulated and scattered, it cannot be excluded that when articulated, the gastralia would have also formed three rows of elements. Finally, the numbers of ossified forefin elements have been demonstrated to vary in the forefin of the basal ichthyosauriform Chaohusaurus9, so the differences in the number of centralia and distal carpals in both specimens of Sclerocormus likely represent intraspecific variation. Because HFUT MJS-16-012 differs notably from the holotype only in its larger body size, we refrain from erecting a new species and tentatively refer the new specimen to S. cf. S. parviceps, pending a detailed comparative study between HFUT MJS-16-012 and the holotype.
The comparison of HFUT MJS-16-012 with the holotype and only specimen of the sympatric Cartorhynchus13 is also of relevance. The exposed area of the quadrate is much smaller than the squamosal in HFUT MJS-16-012, although it is partially covered by the squamosal (Fig. 3). Conversely, the size of the quadrate and squamosal is not much different in Cartorhynchus14. The length of the upper temporal fenestra is significantly longer than that of the orbit in Sclerocormus, unlike the much smaller fenestra in Cartorhynchus13. The symphysis of HFUT MJS-16-012 is long, accounting for nearly 1/3 of the entire lower jaw length, while it is weak and much shorter (1/5 of the lower jaw length) in Cartorhynchus14. The splenials of HFUT MJS-16-012 meet within the symphysis and extend to the tip of the jaw, while they do not in Cartorhynchus14. Cartorhynchus has three functional tooth rows on the right dentary14, and no dental battery23, while HFUT MJS-16-012 only has a single functional tooth row on the lower jaw but has a dental battery in both the upper and lower jaws (Figs. 4a, 5). The interclavicle is anteriorly flat with a small process extending posteriorly in HFUT MJS-16-012 (Fig. 2), yet the bone is cruciform in Cartorhynchus. The number of presacral vertebrae in Sclerocormus is higher than that of Cartorhynchus (34 vs 31). The gastralia are arranged into three sets in HFUT MJS-16-012 and are robust, curved, and flat with grooves on the surface (Figs. 2, 4c), but they have a slender rod-like shape in Cartorhynchus13.
Distal carpal 4 of Sclerocormus is ossified (Fig. 2). However, there are no distal carpals preserved in the Cartorhynchus holotype13. The holotype of Cartorhynchus preserves an almost complete scleral ring, but the aperture of the scleral ring occupies <20% of the entire orbital area. Finally, the neural spines in Cartorhynchus are unfinished in dorsal view13. The above characteristics indicate that the Cartorhynchus holotype likely represents a juvenile individual27, rather than an adult as previously stated, but it is unlikely to be a juvenile ontogenetic stage of Sclerocormus.
Although no complete skull is known for Omphalosaurus, the skull and the snout were likely short as suggested by O. nettarhynchus28, which is consistent with Cartorhynchus and Sclerocormus (Figs. 2, 3). The dentary in Cartorhynchus and Sclerocormus ends posteriorly in a characteristic wing-shaped extension that is raised slightly above the jaw surface (Fig. 4a) and is similar to the Omphalosaurus nevadanus holotype20 and isolated dentaries of Omphalosaurus sp. from Spitsbergen22. The deep and robust splenials, which are similar to those in Omphalosaurus nevadanus20,23,28, reach the tip of the jaw in HFUT MJS-16-012 (Fig. 2). The tooth-bearing parts in the Chinese specimens are distinctly longer in the lower jaw than the upper jaw (Fig. 5)14, as in the Alpine specimen of Omphalosaurus23. In HFUT MJS-16-012, the tooth rows are irregularly arranged (Fig. 5) and hard to define as in the Spitsbergen and Alpine Omphalosaurus22,29. A similar tooth morphology is shared among the new specimen of Sclerocormus (Figs. 4a, 5–8), Cartorhynchus, and Omphalosaurus: low dome-shaped crowns and multiple irregular tooth rows, while only Sclerocormus and Omphalosaurus share obvious ‘orange-peel-like’ pits on the enamel surface (Fig. 8)14,23,24,29,30.
To test the phylogenetic position of Sclerocormus, Cartorhynchus and Omphalosaurus (scoring based mostly on O. nevadanus20 and O. cf. O. nevadanus23), we included these taxa into a modified phylogenetic matrix focusing on the relationships among diapsid reptiles (Supplementary Data 1, 2). Heuristic searches of the diapsid data matrix found eight most parsimonious trees (tree length = 897, consistency index = 0.297, retention index = 0.62). The strict consensus tree with bootstrap nodal support values is shown in Fig. 9 and Supplementary Fig. 3. Our phylogenetic analysis recovered all three taxa as forming a sister clade to Ichthyopterygia, nested within Ichthyosauriformes. Several dental and cranial characters shared between Omphalosaurus, Cartorhynchus and Sclerocormus confirm their monophyly and support the synonymy of the recently erected Nasorostra with Omphalosauridae (see Systematic Palaeontology).
Functional morphospace analysis
To understand the ecology of omphalosaurids, we performed a functional morphospace analysis based on a revised data matrix (Supplementary Data 3, 4)7. PCO 1 and 2 explain nearly 50% of the craniodental morphological variation among Mesozoic marine reptiles. Morphospaces of durophagous forms such as placodonts, the durophagous mosasaur Globidens, and the omphalosaurid Cartorhynchus and Sclerocormus are convergently shifted towards higher PCO 1 and 2 values within each subclade (Sauropterygia, Squamata and Ichthyosauromorpha). However, Cartorhynchus and Sclerocormus do not occupy the morphospace of shallow-marine durophagous marine reptiles, but instead plot beyond the edge of the ichthyosauromorph space among that of marine turtles (Fig. 10).
Cartorhynchus and Sclerocormus, originally assigned to Nasorostra, were previously not considered as omphalosaurids because their dentition was not exposed in the holotypes13,25. Even though durophagous dentition was later identified in Cartorhynchus14, detailed comparisons with the dentition of Omphalosaurus were not made, and the similarity between other characters of the skull to those of Omphalosaurus also went unnoticed. The new specimen of Sclerocormus demonstrates that Nasorostra are synonymous with Omphalosauridae, as evidenced by the tooth morphology, arrangement and replacement (Figs. 4a, 5–8), as well as the presence of an edentulous premaxilla and a wing-like process of the posterior dentary (Figs. 2–4), which are shared between Sclerocormus, Cartorhynchus and Omphalosaurus. Addition of the new specimen into a phylogenetic analysis also provides unambiguous evidence for the ichthyosauriform affinity of omphalosaurids, which are the sister clade to Ichthyopterygia (Fig. 9). The new specimen also supports the taxonomic distinctness of Cartorhynchus and Sclerocormus, because the number of presacral vertebrae is different between them14,25, and the interclavicle in the new specimen possesses only a short process extending posteriorly (Figs. 2, 4b), yet the bone is cruciform in shape in Cartorhynchus13. Such a marked difference in morphology is unlikely to be the result of ontogenetic changes. Currently, Omphalosauridae is represented by three genera spanning the Early–Middle Triassic13,23,25. However, the co-occurrence of two genera in Majiashan quarry alone, and the morphological differences present between different species of Omphalosaurus indicate that the generic diversity of Omphalosauridae is likely underestimated. In fact, two different omphalosaurid morphotypes are also present in the Early Triassic of Svalbard – smaller specimens with teeth bearing clearly differentiated roots, resembling the dentition of Cartorhynchus, and larger specimens with rootless teeth, resembling the dentition of Sclerocormus22. It is uncertain, however, whether these two morphotypes represent intraspecific variability or taxonomic diversity.
The three-dimensionally preserved skull and mandible of the new specimen of Sclerocormus also allow for the reconstruction of the bizarre, specialised feeding apparatus of omphalosaurids for the first time. Prey capture was probably facilitated by the pointed tips of the upper and lower jaws, and the prey was transported towards the oral cavity perhaps with the aid of suction31, although the hyoids are weakly developed in Sclerocormus (Fig. 2). The seemingly durophagous functional dentition of omphalosaurids was not concentrated posteriorly, unlike in most other Triassic marine reptiles12. The lower jaw itself was slender and lacked a well-developed coronoid process, in contrast to the robust lower jaws of placodonts32 and the durophagous mosasaur Globidens33. Furthermore, the rugose surfaces of the maxillae and dentaries bear sharp ridges and pits (Fig. 4a), similar to those in the early turtle Eorhynchochelys34 that probably indicate the presence of a keratinous beak, that would have aided in the processing of hard-shelled prey. Our morphofunctional analysis demonstrates that the lower jaws of omphalosaurids were most similar to those of marine turtles (Fig. 10), which also possess a keratinous beak but lack teeth, and suggests omphalosaurid jaws were capable of capturing pelagic prey and processing a wide range of food items like pelagic foraging turtles35,36,37. The presence of heavily worn and frequently replaced teeth also suggests that omphalosaurids at least partially fed on abrasive hard-shelled invertebrates, especially ammonoids that were found in the same pelagic sediments as omphalosaurids23 (Supplementary Fig. 2).
Our phylogenetic analysis, which demonstrates that Cartorhynchus was the sister-clade of (Sclerocormus + Omphalosaurus), seems to indicate that throughout their evolution, the teeth of omphalosaurids underwent root reduction. An efficient grinding surface formed by numerous teeth dispersed along the occlusal surfaces of the jaw bones likely allowed omphalosaurids to process their food even more efficiently23. Given the lack of modern analogues of the feeding apparatus of omphalosaurids and modern open-water ecosystems dominated by hard-shelled invertebrates, an analysis of feeding and lifestyle in omphalosaurids inherently involves much speculation.
The dentition and feeding apparatus of omphalosaurids differ strikingly from those of other contemporaneous marine reptiles with blunt teeth that were restricted largely to more shallow-marine environments and likely fed on sessile and benthic invertebrates12. Therefore, we argue that omphalosaurids represented a unique lineage of pelagic predators capable of feeding on hard-shelled invertebrates. Even though the body plan of omphalosaurids lacked anatomical features associated with efficient pelagic cruising, they were likely well adapted to a pelagic lifestyle as evidenced by their highly cancellous bone histology, since the disappearance of compact bone in tetrapods is generally a manifestation of more aquatic adaptation23. Furthermore, omphalosaurids do not need to be efficient pursuit predators, as they could have fed on high-density but low-speed pelagic invertebrates such as ammonoids38,39. The fact that omphalosaurids are known almost exclusively from pelagic deposits in which they co-occur with ammonoids also supports our hypothesis.
Cartorhynchus was previously determined to be at least semi-terrestrial on the basis of its highly unossified flippers, low dorsal vertebral count, and relatively weak visual capacity13. However, strongly unossified flippers are also present in the likely fully aquatic basal ichthyosauriform Chaohusaurus9 and the vertebral count of Cartorhynchus also overlaps with the range for some other marine reptiles13. In addition, the seemingly weakly developed underwater vision of Cartorhynchus could still have been useful for detecting pelagic invertebrates, especially in the photic zone13. Therefore, Cartorhynchus is probably a pelagic animal like other omphalosaurids, as also supported by the deep water environment of Majiashan quarry (Supplementary Results; Supplementary Figs. 1, 2).
Omphalosauridae was the most widespread clade of ichthyosauriforms of their times, now known from all important Northern Hemisphere pelagic regions that have produced Early and Middle Triassic marine reptiles, in contrast to other groups of ichthyosauriforms with more restricted distribution in time and space40. Their evolution seems to have tracked the fast recovery of ammonoids41 and conodonts42 in the Early and Middle Triassic. The prevailing view on marine ecosystem recovery after the PTME has been that the shallow-water Middle Triassic biotas rich in sauropterygians are representative for the fully recovered ecosystems around the world1 and that the Early Triassic ichthyosauromorph domination was replaced by Middle Triassic sauropterygian domination25. Our study suggests that the radiation was not only amazingly rapid in shallow-water ecosystems6, but also in the open ocean, as indicated by the evolution of omphalosaurids and colossal macropredatory ichthyosaurs3,43. The broad geographic distribution and high taxonomic and ecomorphological diversity of Early and Middle Triassic ichthyosauriforms underscores their crucial role in the ecosystem recovery after the PTME, adding further evidence to the emerging scenario of rapid ecosystem recovery in its aftermath in the open ocean18.
μCt scan of the skull
The new specimen (HFUT MJS-16-012) was scanned with a micro X-ray computed tomography scanner (NIKON XTH 320/225 LC: 200 kV and 180 mA, voxel size = 0.146 × 0.146 × 0.146 mm) at the X-Ray Computed Tomography and Multi-Scale Simulation Laboratory, School of Civil Engineering and Architecture, Zhejiang University, Hangzhou, China. A total of 3142 slices were generated. The original slices were read into ImageJ 1.52a44 and edited using the Brightness/Contrast tool in order to enhance the contrast between the dental tissues and the surrounding bone and to reduce the effect of beam-hardening. The edited slices were then uploaded into Avizo 2019.4 (Thermo Fischer Scientific). The individual teeth were manually segmented using the Lasso tool.
We modified the recent taxon-character matrix for diapsids with a particular focus on marine reptiles25. The matirx was prepared using Mesquite. Two new characters were added to the original data matrix. Character scores for eight taxa (Parareptilia, Helveticosaurus, Placodus, Largocephalosaurus, Sinosaurosphargis, Wumengosaurus, Simosaurus and Pistosauridae) were modified and Pachypleurosauria was replaced with an Anarosaurus-Dactylosaurus operational taxonomic unit (see Supplementary Data 1 for details). The new specimen (HFUT MJS-16-012) was included in the matrix independently of the holotype of Sclerocormus, and two more taxa, Eusaurosphargis and Omphalosaurus, were included as well. The coding of the holotypes of Cartorhynchus and Sclerocormus was updated based on the recent restudy14, and that of Eusaurosphargis was based on ref. 45. The coding of Omphalosaurus was based on the literature and direct specimen observations. See Supplementary Table 2 for referred specimens, and Supplementary Data 1 for the description of the new characters and the new coding. A heuristic analysis was performed in TNT 1.5 (random seed = 1, Wagner tree replicates = 5000, numbers of trees held per replicate = 10, branch swap algorithm = tree bisection and reconnection)46. All multistate characters were treated as unordered. A bootstrap sampling of 1000 replicates of the dataset was conducted to measure the nodal support. The NEXUS file is available in Supplementary Data 2.
Functional morphospace analysis
A previous data matrix of 18 morphofunctional characters and 207 taxa (Supplementary Data 3)7 was modified for the morphospace analysis. Characters 4–6 were removed due to the subjectivity of assessing the extent of temporal musculature in extinct taxa. Measurements and coding for C. lenticarpus and Sclerocormus (HFUT MJS-16-012) were modified or newly added to the original dataset from published photographs and personal examination. Following the method described in ref. 7, raw continuous data were z-transformed, and a Gower’s distance matrix47 was generated from the combined continuous + discrete data, using the R package StatMatch48. The distance matrix was subjected to principal coordinate analysis (Supplementary Data 4) using the cmdscale function in R49.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary information files.
The authors declare that the code supporting the findings of this study is available in the Supplementary information files.
Chen, Z.-Q. & Benton, M. J. The timing and pattern of biotic recovery following the end-Permian mass extinction. Nat. Geosci. 5, 375–383 (2012).
Song, H., Wignall, P. B. & Dunhill, A. M. Decoupled taxonomic and ecological recoveries from the Permo-Triassic extinction. Sci. Adv. 4, eaat5091 (2018).
Sander, P. M. et al. Early giant reveals faster evolution of large body size in ichthyosaurs than in cetaceans. Science 374, eabf5787 (2021).
Kelley, N. P. & Pyenson, N. D. Evolutionary innovation and ecology in marine tetrapods from the Triassic to the Anthropocene. Science 348, aaa3716 (2015).
Scheyer, T. M., Romano, C., Jenks, J. & Bucher, H. Early Triassic marine biotic recovery: the predators’ perspective. PLoS One 9, e88987 (2014).
Motani, R. et al. Lunge feeding in early marine reptiles and fast evolution of marine tetrapod feeding guilds. Sci. Rep. 5, 8900 (2015).
Stubbs, T. L. & Benton, M. J. Ecomorphological diversifications of Mesozoic marine reptiles: the roles of ecological opportunity and extinction. Paleobiology 42, 547–573 (2016).
Moon, B. C. & Stubbs, T. L. Early high rates and disparity in the evolution of ichthyosaurs. Commun. Biol. 3, 68 (2020).
Huang, J.-D. et al. The new ichthyosauriform Chaohusaurus brevifemoralis (Reptilia, Ichthyosauromorpha) from Majiashan, Chaohu, Anhui Province, China. PeerJ 7, e7561 (2019).
Li, Q. & Liu, J. An Early Triassic sauropterygian and associated fauna from South China provide insights into Triassic ecosystem health. Commun. Biol. 3, 63 (2020).
Cheng, L. et al. Early Triassic marine reptile representing the oldest record of unusually small eyes in reptiles indicating non-visual prey detection. Sci. Rep. 9, 152 (2019).
Kelley, N. P., Motani, R., Jiang, D.-Y., Rieppel, O. & Schmitz, L. Selective extinction of Triassic marine reptiles during long-term sea-level changes illuminated by seawater strontium isotopes. Palaeogeogr., Palaeoclimatol. Palaeoecol. 400, 9–16 (2014).
Motani, R. et al. A basal ichthyosauriform with a short snout from the Lower Triassic of China. Nature 517, 485–488 (2015).
Huang, J.-D. et al. Repeated evolution of durophagy during ichthyosaur radiation after mass extinction indicated by hidden dentition. Sci. Rep. 10, 7798 (2020).
Rieppel, O. Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas. Zool. J. Linn. Soc.-Lond. 135, 33–63 (2002).
Druckenmiller, P. S., Kelley, N. P., Metz, E. T. & Baichtal, J. An articulated Late Triassic (Norian) thalattosauroid from Alaska and ecomorphology and extinction of Thalattosauria. Sci. Rep. 10, 1746 (2020).
Hu, S. X. et al. The Luoping biota: exceptional preservation, and new evidence on the Triassic recovery from end-Permian mass extinction. Proc. R. Soc. B Biol. Sci. 278, 2274–2282 (2011).
Brayard, A. et al. Good genes and good luck: ammonoid diversity and the end-Permian mass extinction. Science 325, 1118–1121 (2009).
Klompmaker, A. A., Waljaard, N. A. & Fraaije, R. H. Ventral bite marks in Mesozoic ammonoids. Palaeogeogr., Palaeoclimatol., Palaeoecol. 280, 245–257 (2009).
Merriam, J. C. Preliminary note on a new marine reptile from the Middle Triassic of Nevada. Univ. Calif. Publ., Bull. Dep. Geol. 5, 71–79 (1906).
Motani, R. Is Omphalosaurus ichthyopterygian? A phylogenetic perspective. J. Vertebr. Paleontol. 20, 295–301 (2000).
Ekeheien, C. P., Delsett, L. L., Roberts, A. J. & Hurum, J. H. Preliminary report on ichthyopterygian elements from the Early Triassic (Spathian) of Spitsbergen. Nor. J. Geol./Nor. Geologisk Foren. 98, 219–238 (2018).
Sander, P. M. & Faber, C. The Triassic marine reptile Omphalosaurus: osteology, jaw anatomy, and evidence for ichthyosaurian affinities. J. Vertebr. Paleontol. 23, 799–816 (2003).
Wintrich, T., Hagdorn, H. & Sander, P. M. An enigmatic marine reptile—the actual first record of Omphalosaurus in the Muschelkalk of the Germanic Basin. J. Vertebr. Paleontol. 37, e1384739 (2017).
Jiang, D.-Y. et al. A large aberrant stem ichthyosauriform indicating early rise and demise of ichthyosauromorphs in the wake of the end-Permian extinction. Sci. Rep. 6, 26232 (2016).
Motani, R., Jiang, D.-Y., Tintori, A., Rieppel, O. & Chen, G.-B. Terrestrial origin of viviparity in Mesozoic marine reptiles indicated by Early Triassic embryonic fossils. PLoS One 9, e88640 (2014).
Fernandez, M. S., Archuby, F., Talevi, M. & Ebner, R. Ichthyosaurian eyes: paleobiological information content in the sclerotic ring of Caypullisaurus (Ichthyosauria, Ophthalmosauria). J. Vertebr. Paleontol. 25, 330–337 (2005).
Mazin, J. M. & Bucher, H. A new interpretation of the type specimen of Omphalosaurus nevadanus Merriam 1906. Palaeontographica. Abt. A Paläozoologie Stratigraphie 195, 19–27 (1986).
Sander, P. M. & Faber, C. New finds of Omphalosaurus and a review of Triassic ichthyosaur paleobiogeography. Paläeontologische Z. 72, 149–162 (1998).
Merriam, J. C. & Bryant, H. C. Notes on the dentition of Omphalosaurus. University of California Publications. Bull. Dep. Geol. 6, 329–332 (1911).
Motani, R. et al. Absence of suction feeding ichthyosaurs and its implications for Triassic mesopelagic paleoecology. PLoS One 8, e66075 (2013).
Neenan, J. M., Li, C., Rieppel, O. & Scheyer, T. M. The cranial anatomy of Chinese placodonts and the phylogeny of Placodontia (Diapsida: Sauropterygia). Zool. J. Linn. Soc. Lond. 175, 415–428 (2015).
Leblanc, A. R. H., Mohr, S. R. & Caldwell, M. W. Insights into the anatomy and functional morphology of durophagous mosasaurines (Squamata: Mosasauridae) from a new species of Globidens from Morocco. Zool. J. Linn. Soc.-Lond. 186, 1026–1052 (2019).
Li, C., Fraser, N. C., Rieppel, O. & Wu, X.-C. A Triassic stem turtle with an edentulous beak. Nature 560, 476–479 (2018).
Palmer, J. L. et al. Dietary analysis of two sympatric marine turtle species in the eastern Mediterranean. Mar. Biol. 168, 94 (2021).
Parham, J. F. & Pyenson, N. D. New sea turtle from the Miocene of Peru and the iterative evolution of feeding ecomorphologies since the Cretaceous. J. Paleontol. 84, 231–247 (2010).
Laffoley, D.d’A. et al. The Protection and Management of the Sargasso Sea (Sargasso Sea Alliance, 2011).
Jacobs, D. K. & Chamberlain, J. A. In Ammonoid Paleobiology (eds Landman, N. H. et al.) 169–224 (Springer, Boston, MA, 1996).
Naglik, C., Tajika, A., Chamberlain, J. & Klug, C. In Ammonoid Paleobiology: From Anatomy to Ecology (eds Klug, C. et al.) 649–688 (Springer, Dordrecht, 2015).
Bardet, N. et al. Mesozoic marine reptile palaeobiogeography in response to drifting plates. Gondwana Res 26, 869–887 (2014).
Brayard, A. et al. Good genes and good luck: ammonoid diversity and the end-Permian mass extinction. Science 325, 1118–1121 (2009).
Orchard, M. J. Conodont diversity and evolution through the latest Permian and Early Triassic upheavals. Palaeogeogr. Palaeoclimatol. Palaeoecol. 252, 93–117 (2007).
Fröbisch, N. B., Fröbisch, J., Sander, P. M., Schmitz, L. & Rieppel, O. Macropredatory ichthyosaur from the Middle Triassic and the origin of modern trophic networks. Proc. Natl Acad. Sci. USA 110, 1393–1397 (2013).
Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671–675 (2012).
Scheyer, T. M. et al. A new, exceptionally preserved juvenile specimen of Eusaurosphargis dalsassoi (Diapsida) and implications for Mesozoic marine diapsid phylogeny. Sci. Rep. 7, 4406 (2017).
Goloboff, P. A. & Catalano, S. A. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32, 221–238 (2016).
Gower, J. C. A general coefficient of similarity and some of its properties. Biometrics https://doi.org/10.2307/2528823 (1971).
D’Orazio, M. Package ‘StatMatch’ (CRAN, 2020).
R Core Team. R: a Language and Environment For Statistical Computing (R Core Team, 2021).
Bureau of Geology and Mineral Resources of Anhui Province. Regional Geology of Anhui Province. (Springer, 1987)
We thank R. Motani and T.L. Stubbs for providing original versions of the phylogenetic and morphospace data matrices, respectively, and the Willi Hennig Society for the TNT programme. We also thank HFUT Paleontology Lab members for field assistance, Y.J. Chen for the preparation of Supplementary Fig. 1, and Z. Xiong, F. Huang, L. Li and T. Sato for fossil preparation. The research was supported by the following grants: National Natural Science Foundation of China (42172026 and 41772003 to J.L., 42202006 to A.S.W., 42002021 to M.I., and 41902104 to Y.S.); Fundamental Research Funds for the Central Universities of China (PA2020GDKC0022 to J.L.); Department of Natural Resources of Anhui Province (2021-g-2-16 to J.L.); German Research Foundation (WI 5353/2-1 to T.W. and P.M.S.); China Scholarship Council (202106690044 to Y.Q.); Humboldt Foundation (to J.L. and P.M.S.); and China Postdoc Council (to A.S.W. and M.I.).
The authors declare no competing interests.
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Qiao, Y., Liu, J., Wolniewicz, A.S. et al. A globally distributed durophagous marine reptile clade supports the rapid recovery of pelagic ecosystems after the Permo-Triassic mass extinction. Commun Biol 5, 1242 (2022). https://doi.org/10.1038/s42003-022-04162-6
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