Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

The oldest gnathostome teeth

Abstract

Mandibular teeth and dentitions are features of jawed vertebrates that were first acquired by the Palaeozoic ancestors1,2,3 of living chondrichthyans and osteichthyans. The fossil record currently points to the latter part of the Silurian period4,5,6,7 (around 425 million years ago) as a minimum date for the appearance of gnathostome teeth and to the evolution of growth and replacement mechanisms of mandibular dentitions in the subsequent Devonian period2,8,9,10. Here we provide, to our knowledge, the earliest direct evidence for jawed vertebrates by describing Qianodus duplicis, a new genus and species of an early Silurian gnathostome based on isolated tooth whorls from Guizhou province, China. The whorls possess non-shedding teeth arranged in a pair of rows that demonstrate a number of features found in modern gnathostome groups. These include lingual addition of teeth in offset rows and maintenance of this patterning throughout whorl development. Our data extend the record of toothed gnathostomes by 14 million years from the late Silurian into the early Silurian (around 439 million years ago) and are important for documenting the initial diversification of vertebrates. Our analyses add to mounting fossil evidence that supports an earlier emergence of jawed vertebrates as part of the Great Ordovician Biodiversification Event (approximately 485–445 million years ago).

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Tooth whorls of Q.duplicis, and their position in the Rongxi Formation exposed at Leijiatun (Shiqian–Tunping section), Guizhou province, China.
Fig. 2: Tooth patterning and tissue structure of Q.duplicis whorls.
Fig. 3: Examples of the earliest chondrichthyan and osteichthyan tooth whorls.

Similar content being viewed by others

Data availability

The tomography slices (bmp), volume renderings (obj) and phylogenetic analyses related files (nex, tnt, tre, xlxs and rft) collected or produced during this study (Supplementary Data 1–6) are available at https://doi.org/10.6084/m9.figshare.20366757.v1. The ZooBank LSID code for this publication is urn:lsid:zoobank.org:pub:F2565F74-5E03-482D-9FDA-72705EB36966. The ZooBank LSID code for the new genus Qianodus is urn:lsid:zoobank.org:act:A072F8AA-1AAF-4837-9F70-F98A4113E606. The ZooBank LSID code for the new species Q.duplicis is urn:lsid:zoobank.org:act:D85084C9-36CC-471E-9E52-51DCB3429618. The examined tooth whorl specimens IVPP V26641–V26663 are available on request from the Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing, China.

References

  1. Donoghue, P. C. & Rücklin, M. The ins and outs of the evolutionary origin of teeth. Evol. Dev. 18, 19–30 (2016).

    Article  PubMed  Google Scholar 

  2. Smith, M. M. Vertebrate dentitions at the origin of jaws: when and how pattern evolved. Evol. Dev. 5, 394–413 (2003).

    Article  PubMed  Google Scholar 

  3. Vaškaninová, V. et al. Marginal dentition and multiple dermal jawbones as the ancestral condition of jawed vertebrates. Science 369, 211–216 (2020).

    Article  ADS  PubMed  Google Scholar 

  4. Chen, D., Blom, H., Sanchez, S., Tafforeau, P. & Ahlberg, P. E. The stem osteichthyan Andreolepis and the origin of tooth replacement. Nature 539, 237–241 (2016).

    Article  ADS  PubMed  Google Scholar 

  5. Chen, D. et al. Development of cyclic shedding teeth from semi-shedding teeth: the inner dental arcade of the stem osteichthyan Lophosteus. R. Soc. Open Sci. 4, 161084 (2017).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  6. Choo, B., Zhu, M., Zhao, W. & Jia, L. The largest Silurian vertebrate and its palaeoecological implications. Sci. Rep. 4, 5242 (2014).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  7. Zhu, M. et al. The oldest articulated osteichthyan reveals mosaic gnathostome characters. Nature 458, 469–474 (2009).

    Article  ADS  CAS  PubMed  Google Scholar 

  8. Denison, R. H. Placodermi Vol. 2 (Gustav Fischer, 1978).

  9. Ginter, M., Hampe, O., Duffin, C. J. & Schultze, H. Handbook of Paleoichthyology Volume 3D. Chondrichthyes. Paleozoic Elasmobranchii: Teeth (Dr Friedrich Pfeil, 2010).

  10. Rücklin, M. et al. Development of teeth and jaws in the earliest jawed vertebrates. Nature 491, 748–751 (2012).

    Article  ADS  PubMed  Google Scholar 

  11. Brazeau, M. D. & Friedman, M. The origin and early phylogenetic history of jawed vertebrates. Nature 520, 490–497 (2015).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  12. Sansom, I. J. & Andreev, P. S. in Evolution and Development of Fishes (eds Johanson, Z. et al.) 59–70 (Cambridge Univ. Press, 2019).

  13. Thanh, T.-D., Phuong, T. H., Boucot, A. J., Goujet, D. & Janvier, P. Silurian vertebrates from Central Vietnam. C. R. Acad. Sci. Paris 324, 1023–1030 (1997).

    Google Scholar 

  14. Zhao, W.-J. et al. A review of Silurian fishes from north-western Hunan, China and related biostratigraphy. Acta Geol. Pol. 68, 475–486 (2018).

  15. Zhu, M. et al. A Silurian maxillate placoderm illuminates jaw evolution. Science 354, 334–336 (2016).

    Article  ADS  CAS  PubMed  Google Scholar 

  16. Burrow, C. J. & Rudkin, D. Oldest near-complete acanthodian: the first vertebrate from the Silurian Bertie Formation Konservat-Lagerstätte, Ontario. PLoS ONE 9, e104171 (2014).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  17. Brazeau, M. D. A revision of the anatomy of the Early Devonian jawed vertebrate Ptomacanthus anglicus Miles. Palaeontology 55, 355–367 (2012).

    Article  Google Scholar 

  18. Burrow, C. J., Davidson, R. G., Den Blaauwen, J. L. & Newman, M. J. Revision of Climatius reticulatus Agassiz, 1844 (Acanthodii, Climatiidae), from the Lower Devonian of Scotland, based on new histological and morphological data. J. Vertebr. Paleontol. 35, e913421 (2015).

    Article  Google Scholar 

  19. Burrow, C. J., Newman, M., Den Blaauwen, J., Jones, R. & Davidson, R. The Early Devonian ischnacanthiform acanthodian Ischnacanthus gracilis (Egerton, 1861) from the Midland Valley of Scotland. Acta Geol. Pol. 68, 335–362 (2018).

    Google Scholar 

  20. Maisey, J. et al. in Evolution and Development of Fishes (eds Johanson, Z. et al.) 87–109 (Cambridge Univ. Press, 2019).

  21. Burrow, C. J. & Simpson, A. J. A new ischnacanthid acanthodian from the Late Silurian (Ludlow, ploeckensis Zone) Jack Formation, north Queensland. Mem. Queensl. Mus. 38, 383–396 (1995).

    Google Scholar 

  22. Gross, W. Mundzähne und Hautzähne der Acanthodier und Arthrodiren. Palaeontogr. Abt. A 12, 1–40 (1957).

  23. Martínez-Pérez, C. et al. Vascular structure of the earliest shark teeth. Acta Geol. Pol. 68, 335–362 (2018).

    Google Scholar 

  24. Coates, M. I. et al. An early chondrichthyan and the evolutionary assembly of a shark body plan. Proc. R. Soc. B 285, 20172418 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  25. Andreev, P. S. et al. The systematics of the Mongolepidida (Chondrichthyes) and the Ordovician origins of the clade. PeerJ 4, e1850 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  26. Andreev, P. S. et al. Early Silurian chondrichthyans from the Tarim Basin (Xinjiang, China). PLoS ONE 15, e0228589 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Keating, J. N., Marquart, C. L. & Donoghue, P. C. Histology of the heterostracan dermal skeleton: insight into the origin of the vertebrate mineralised skeleton. J. Morph. 276, 657–680 (2015).

    Article  PubMed  Google Scholar 

  28. Dearden, R. P., Stockey, C. & Brazeau, M. D. The pharynx of the stem-chondrichthyan Ptomacanthus and the early evolution of the gnathostome gill skeleton. Nat. Commun. 10, 2050 (2019).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  29. Gegenbaur, C. Grundriss der Vergleichenden Anatomie (Wilhelm Engelmann, 1874).

  30. Huxley, T. H. On the application of the laws of evolution to the arrangement of the Vertebrata, and more particularly of the Mammalia. Proc. Sci. Meet. Zool. Soc. Lond. 1880, 649–662 (1880).

    Google Scholar 

  31. Rücklin, M. et al. Acanthodian dental development and the origin of gnathostome dentitions. Nat. Ecol. Evol. 5, 919–926 (2021).

    Article  PubMed  Google Scholar 

  32. Maisey, J. G., Turner, S., Naylor, G. J. & Miller, R. F. Dental patterning in the earliest sharks: implications for tooth evolution. J. Morph. 275, 586–596 (2014).

    PubMed  Google Scholar 

  33. Underwood, C., Johanson, Z. & Smith, M. M. Cutting blade dentitions in squaliform sharks form by modification of inherited alternate tooth ordering patterns. R. Soc. Open Sci. 3, 160385 (2016).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  34. Underwood, C. J. et al. Development and evolution of dentition pattern and tooth order in the skates and rays (Batoidea; Chondrichthyes). PLoS ONE 10, e0122553 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  35. Smith, M. M. & Coates, M. I. in Major Events in Early Vertebrate Evolution (ed. Ahlberg, P. E.) 223–240 (Taylor & Francis, 2001).

  36. Coates, M. & Sequeira, S. A new stethacanthid chondrichthyan from the Lower Carboniferous of Bearsden, Scotland. J. Vertebr. Paleontol. 21, 438–459 (2001).

    Article  Google Scholar 

  37. Zangerl, R. & Case, G. Cobelodus aculeatus (Cope), an anacanthous shark from Pennsylvanian black shales of North America. Palaeontogr. Abt. A 154, 107–157 (1976).

    Google Scholar 

  38. Andrews, M., Long, J., Ahlberg, P., Barwick, R. & Campbell, K. The structure of the sarcopterygian Onychodus jandemarrai n. sp. from Gogo, Western Australia: with a functional interpretation of the skeleton. Earth. Env. Sci. Trans. R. Soc. Edinb. 96, 197–307 (2005).

    Article  Google Scholar 

  39. Blais, S. A., MacKenzie, L. A. & Wilson, M. V. Tooth-like scales in Early Devonian eugnathostomes and the ‘outside-in’ hypothesis for the origins of teeth in vertebrates. J. Vertebr. Paleontol. 31, 1189–1199 (2011).

    Article  Google Scholar 

  40. Frey, L. et al. The early elasmobranch Phoebodus: phylogenetic relationships, ecomorphology and a new time-scale for shark evolution. Proc. R. Soc. B 286, 20191336 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  41. Hu, Y., Lu, J. & Young, G. C. New findings in a 400 million-year-old Devonian placoderm shed light on jaw structure and function in basal gnathostomes. Sci. Rep. 7, 7813 (2017).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  42. Hu, Y.-Z., Young, G., Burrow, C., Zhu, Y.-A. & Lu, J. High resolution XCT scanning reveals complex morphology of gnathal elements in an Early Devonian arthrodire. Palaeoworld 28, 525–534 (2019).

    Article  Google Scholar 

  43. Doeland, M., Couzens, A. M., Donoghue, P. C. & Rücklin, M. Tooth replacement in early sarcopterygians. R. Soc. Open Sci. 6, 191173 (2019).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  44. Zhu, M. & Yu, X. in Recent Advances in the Origin and Early Radiation of Vertebrates (eds Arratia, G. et al.) 271–286 (Dr. Friedrich Pfeil, 2004).

  45. Burrow, C. J., Newman, M. J., Davidson, R. G. & den Blaauwen, J. L. Redescription of Parexus recurvus, an Early Devonian acanthodian from the Midland Valley of Scotland. Alcheringa 37, 392–414 (2013).

    Article  Google Scholar 

  46. Dearden, R. P. & Giles, S. Diverse stem-chondrichthyan oral structures and evidence for an independently acquired acanthodid dentition. R. Soc. Open Sci. 8, 210822 (2021).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  47. Zangerl, R. & Case, G. R. Iniopterygia, a New Order of Chondrichthyan Fishes from the Pennsylvanian of North America (Field Museum of Natural History, 1973).

  48. Andreev, P. S. et al. Upper Ordovician chondrichthyan‐like scales from North America. Palaeontology 58, 691–704 (2015).

    Article  Google Scholar 

  49. Servais, T. & Harper, D. A. The great Ordovician biodiversification event (GOBE): definition, concept and duration. Lethaia 51, 151–164 (2018).

    Article  Google Scholar 

  50. Wang, C.-C. Joint iterative fast projection matching for fully automatic marker-free alignment of nano-tomography reconstructions. Sci. Rep. 10, 7330 (2020).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  51. Wang, Y. et al. Development and applications of paleontological computed tomography. Vertebr. PalAsiat. 57, 84–92 (2019).

    Google Scholar 

  52. Goloboff, P. A. & Catalano, S. A. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32, 221–238 (2016).

    Article  PubMed  Google Scholar 

  53. Brazeau, M. et al. Endochondral bone in an Early Devonian ‘placoderm’ from Mongolia. Nat. Ecol. Evol. 4, 1477–1484 (2020).

    Article  PubMed  Google Scholar 

  54. Dearden, R. P. The Anatomy and Evolution ofAcanthodianStem-chondrichthyans. PhD thesis, Imperial College London (2018).

  55. Giles, S., Friedman, M. & Brazeau, M. D. Osteichthyan-like cranial conditions in an Early Devonian stem gnathostome. Nature 520, 82–85 (2015).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  56. King, B., Qiao, T., Lee, M. S., Zhu, M. & Long, J. A. Bayesian morphological clock methods resurrect placoderm monophyly and reveal rapid early evolution in jawed vertebrates. Syst. Biol. 66, 499–516 (2017).

    PubMed  Google Scholar 

  57. Qiao, T., King, B., Long, J. A., Ahlberg, P. E. & Zhu, M. Early gnathostome phylogeny revisited: multiple method consensus. PLoS ONE 11, e0163157 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  58. Zhu, Y.-a, Lu, J. & Zhu, M. Reappraisal of the Silurian placoderm Silurolepis and insights into the dermal neck joint evolution. R. Soc. Open Sci. 6, 191181 (2019).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  59. Bapst, D. W. paleotree: an R package for paleontological and phylogenetic analyses of evolution. Methods Ecol. Evol. 3, 803–807 (2012).

    Article  Google Scholar 

  60. Botella, H., Manzanares, E., Ferrón, H. & Martínez-Pérez, C. Obruchevacanthus ireneae gen. et sp. nov., a new ischnacanthiform (Acanthodii) from the Lower Devonian of Spain. Paleontol. J. 48, 1067–1076 (2014).

    Article  Google Scholar 

  61. Gagnier, P.-Y. & Wilson, M. V. An unusual acanthodian from northern Canada: revision of Brochoadmones milesi. Mod. Geol. 20, 235–252 (1996).

    Google Scholar 

  62. Jarvik, E. Middle and Upper Devonian Porolepiformes from East Greenland with special reference to Glyptolepis groenlandica n. sp. and a discussion on the structure of the head in the Porolepiformes. Medd. Grønl. 187, 1–307 (1972).

  63. Long, J. New palaeoniscoid fishes from the Late Devonian and Early Carboniferous of Victoria. Mem. Assoc. Australas. Palaeontol. 7, 1–64 (1988).

    Google Scholar 

  64. Miles, R. S. Articulated acanthodian fishes from the Old Red Sandstone of England: with a review of the structure and evolution of the acanthodian shoulder-girdle. Bull. Br. Mus. Nat. Hist. Geol. 24, 111–213 (1973).

    MathSciNet  Google Scholar 

  65. Mondéjar‐Fernández, J., Friedman, M. & Giles, S. Redescription of the cranial skeleton of the Early Devonian (Emsian) sarcopterygian Durialepis edentatus Otto (Dipnomorpha, Porolepiformes). Pap. Palaeontol. 7, 789–806 (2020).

  66. Qu, Q., Sanchez, S., Blom, H., Tafforeau, P. & Ahlberg, P. E. Scales and tooth whorls of ancient fishes challenge distinction between external and oral ‘teeth’. PLoS ONE 8, e71890 (2013).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  67. Vergoossen, J. Late Silurian fish microfossils from Helvetesgraven, Skåne (southern Sweden) (I). Geol. Mijnbouw 78, 267–280 (1999).

    Article  Google Scholar 

  68. Wang, N.-Z. Microremains of agnathans and fishes from Lower Devonian of central Guangxi with correlation of Lower Devonian between central Guangxi and eastern Yunnan, South China. Acta Palaeontol. Sin. 31, 280–303 (1992).

    Google Scholar 

Download references

Acknowledgements

We thank J.-C. Cai for the field work, Y.-M. Hou for the acquisition of the micro-computed tomography X-ray data, Y. Hwu and Y.-T. Weng for performing and assisting with the synchrotron X-ray analyses and Y. Z. Hu for her comments and advice during the preparation of tooth-whorl volume renderings in Drishti. This research was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA19050102 and XDB26000000), the National Natural Science Foundation of China (42130209), the Key Research Program of Frontier Sciences, CAS (QYZDJ-SSW-DQC002), an Open Project Grant of the Key Laboratory of Vertebrate Evolution and Human Origins, IVPP, CAS (LVEHO19001), MOST 108-2116-M-213-001 (Taiwan), Chinese Postdoctoral Science Foundation grant (2019M663440) and the National Synchrotron Radiation Research Center, Taiwan (beamtime projects 2019-3-083-1 and 2019-3-185-1).

Author information

Authors and Affiliations

Authors

Contributions

Research design: M.Z., P.S.A. and I.J.S. Fieldwork and sample collection: M.Z., W.Z., Q.L., J.W., L.J., T.Q. and L.P. Data processing: Q.L., P.S.A., L.P., J.W. and M.Z. Synchrotron X‐ray tomography analyses: P.S.A. and C.-C.W. Manuscript text and figure preparation: P.S.A., I.J.S., Q.L., J.W. and M.Z.

Corresponding author

Correspondence to Min Zhu.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Nature thanks Matt Friedman and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Extended data figures and tables

Extended Data Fig. 1 Morphology of Qianodus tooth whorls.

(a–c, i, j, m) Scanning electron microscopy, volume renderings of (g, h) synchrotron and (df) microcomputed X-ray tomography datasets and (k, l, n) light microscopy. (a) Lateral (mesial or distal) view of a heavily abraded tooth whorl (IVPP V26648). (b) Mesial view of a tooth whorl (IVPP V26649). (c) Latero-posterior view of a tooth whorl (IVPP V26652). (d–f) Tooth whorl (IVPP V26647) in (d) labial, (e) mesial and (f) basal views. (g, h) Incomplete tooth (IVPP V26645) whorl in (g) mesial and (h) basal views. (i) Lateral view of a tooth whorl (IVPP V26654) with a flared-out base. (jn) Two complete whorls with 6 recognizable primary teeth in (j, k) lateral (distal and mesial) (IVPP V26650), (m) oral (IVPP V26651) and (l, n) basal (IVPP V26650, 51) views. at, accessory teeth; la, labial, li, lingual; pt, primary teeth. Scale bars, 0.5 mm.

Extended Data Fig. 2 Internal structure of Qianodus tooth whorls.

(a, g) Nomarski DIC optical microscopy and (bf, h) volume renderings of synchrotron X-ray tomography datasets. (a) Longitudinal thin section through a whorl with partially preserved teeth IVPP V26653. (b) Longitudinal virtual slice through the progenitor tooth row of the holotype IVPP V26641. (c) Horizontal virtual slice through the holotype IVPP V26641 at the level of tooth. (d) Transverse virtual slice through a partially preserved whorl IVPP V26645. (e) Basal view of IVPP V26641 with highlighted compact tissue of the base. (f) Volume rendering of radiotransparent structures inside a tooth whorl fragment (IVPP V26646) shown in oral view. (g) Longitudinal thin section and (h) longitudinal virtual section through IVPP V26646. at, accessory teeth; ct, compact tissue; la, labial; li, lingual; p, tooth pulp; pt, primary teeth; st, spongiose tissue; stc, spongiose tissue canals; wbc, whorl base crest. Scale bars, 0.5 mm.

Extended Data Fig. 3 Comparison of Qianodus tooth whorls with the whorl-based dentition of the stem chondrichthyan Doliodus problematicus.

(a) Qianodus tooth whorls at a late stage of development (from top to bottom IVPP V26652, V26641, V26649, V26647, V26655 and V26648). (b) Tooth whorls of the lower left jaw ramus of Doliodus at positions 1 to 9 (P1–9) (adapted from Maisey et al.32).

Extended Data Fig. 4 Phylogenetic position of Qianodus within early jawed vertebrates.

50 percent majority-rule consensus tree from a parsimony analysis of 105 taxa and 294 characters. Tree time-adjusted using minimum branch length scaling. Taxon and tree root ages sourced from King et al.56 and other studies (for a full list of studies, see Supplementary Table 1). Colour coding of cladogram branches: jawless stem gnathostomes (purple), ‘placoderms’ (black), Osteichthyes (green), stem Chondrichthyes (ochre), crown Chondrichthyes (blue). Pie charts represent Markov k-state 1 likelihood values for tooth whorl/dentition characters at select internal nodes. Circles show character states at terminal nodes. Character numbers shown in parentheses.

Extended Data Fig. 5 Results of the parsimony analysis described in the Methods section and in Extended Data Fig. 4.

(a) 50% majority-rule consensus and (b) strict consensus tree topologies. Squares in (a) depict most-parsimonious character state reconstructions at select internal nodes (character numbers shown in parentheses). Numbers at internal branches represent bootstrap values of 50 percent and above.

Supplementary information

Supplementary Information

(1) Geological setting and biostratigraphy of the Rongxi Formation. (2) Character list for the phylogenetic analysis. (3) Supplementary Table 1. (4) Supplementary references. Supplementary Data files 1–6 are available online at https://doi.org/10.6084/m9.figshare.20366757.v1. These include the tomography slices (bmp), volume renderings (obj) and phylogenetic analyses related files (nex, tnt, tre, xlxs and rft) collected or produced during this study.

Reporting Summary

Peer Review File

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Andreev, P.S., Sansom, I.J., Li, Q. et al. The oldest gnathostome teeth. Nature 609, 964–968 (2022). https://doi.org/10.1038/s41586-022-05166-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41586-022-05166-2

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing