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Nine evidence mosaics in turtle and lepidosaur origins

Move from named bones and CT volumes to competing matrices, clock calibrations and explicit Mosasauroidea–Mosasauridae boundaries without turning separate fossils into an ancestor ladder.

Each step names its evidence claims, with references below. Interactive Explorer states are available in the full application; the narrative remains an editorial synthesis.

Story sequence

01 · 262.3 Ma · evidence

A rib section tests a shell model

NHM PV R 4949 shows successive bone deposition in a broadened Eunotosaurus rib, while other specimens preserve shoulder anatomy. The tissue is observed; turtle-stem placement, homology and function are tested interpretations.

Separate preserved tissue from a character-homology model and from direct ancestry.

claim:event:eunotosaurus-rib-histology-shell-model
02 · 239.5 Ma · evidence

Paired gastralia without a finished plastron

The Vellberg Pappochelys sample combines broad ribs and robust paired gastralia but lacks a fused plastron and complete carapace. Serial fusion is a homology hypothesis, not a frame in a literal ancestor sequence.

A multi-specimen reconstruction is not one individual transforming into a later taxon.

claim:event:pappochelys-gastralia-shell-mosaic
03 · 232.15 Ma · evidence

A complete plastron and incomplete dorsal shell

Three Odontochelys specimens preserve a developed plastron with expanded ribs and neural plates but no complete carapace. A plastron-first sequence and marginal-marine life remain interpretations, not anatomy seen changing through time.

Shell elements, environmental setting and a proposed evolutionary order are distinct claim layers.

claim:event:odontochelys-plastron-dorsal-shell-mosaic
04 · 155.6 Ma · tree

One fossil sets a minimum, not an origin date

Caribemys holotype MNHNCu P-3209 anchors a 155.6 Ma hard minimum for crown Testudines in one best-practice analysis. Its much older posterior estimate comes from a relaxed clock, topology and priors.

A fossil minimum, a maximum prior and a posterior node age are three different quantities.

claim:event:caribemys-crown-turtle-calibration
05 · 228.65 Ma · tree

A three-dimensional skull enters several trees

Micro-CT reveals the cranial mosaic of Taytalura holotype PVSJ 698. Multiple analyses place it on the lepidosauromorph stem, but a single skull does not supply whole-body anatomy, direct ancestry or a global range.

The scan volume is specimen evidence; the tree position is an analytical output.

claim:event:taytalura-stem-lepidosaur-skull
06 · 244.6 Ma · tree

One skeleton joins morphology and molecules

CT anatomy of Megachirella PZO 628 was combined with fossil morphology and living molecular partitions. The analysis recovers a stem squamate and estimates deep divergences, but neither output is a directly observed crown FAD.

Fossil anatomy, molecular constraint and clock time remain separately labelled.

claim:event:megachirella-ct-stem-squamate
07 · 166.75 Ma · evidence

A near-complete skeleton still gives a mosaic

Synchrotron scans of Bellairsia NMS G.2022.1.1 reveal crown-like and retained states in one Jurassic skeleton. Stem placement and proposed cranial motion depend on matrices and functional interpretation.

Completeness improves observation but does not remove topology or function uncertainty.

claim:event:bellairsia-synchrotron-stem-squamate
08 · 203.55 Ma · evidence

The same block supports competing placements

Teams disagree over bones, referrals and character scores for Cryptovaranoides NHMUK PV R36822, producing crown-squamate and non-squamate trees. The atlas therefore keeps the topology contested instead of inventing a secure Triassic crown FAD.

COL26.8 assigns 12,622 accepted living species to this package as a nomenclatural routing snapshot; it neither resolves fossil topology nor measures dossier, translation, media or review maturity.

claim:event:cryptovaranoides-competing-topologies
09 · 92 Ma · evidence

A superfamily is not the same as its true mosasaur family

Explicit definitions make Mosasauroidea broader than node-defined Mosasauridae. Dallasaurus retains plesiopedal limbs, so family placement and full paddle specialization remain separate questions.

The Mosasauroidea navigation edge is non-taxonomic for discovery; basal topology remains analysis-sensitive.

claim:event:mosasauroid-clade-boundaries

References

  1. Evolutionary Origin of the Turtle ShellLyson, T.R.; Bever, G.S.; Scheyer, T.M.; Hsiang, A.Y.; Gauthier, J.A. · 2013 · DOI 10.1016/j.cub.2013.05.003
  2. A Middle Triassic stem-turtle and the evolution of the turtle body planSchoch, R.R.; Sues, H.-D. · 2015 · DOI 10.1038/nature14472
  3. An ancestral turtle from the Late Triassic of southwestern ChinaLi, C.; Wu, X.-C.; Rieppel, O.; Wang, L.-T.; Zhao, L.-J. · 2008 · DOI 10.1038/nature07533
  4. A Divergence Dating Analysis of Turtles Using Fossil Calibrations: An Example of Best PracticesJoyce, W.G.; Parham, J.F.; Lyson, T.R.; Warnock, R.C.M.; Donoghue, P.C.J. · 2013 · DOI 10.1666/12-149
  5. A Triassic stem lepidosaur illuminates the origin of lizard-like reptilesMartínez, R.N.; Simões, T.R.; Sobral, G.; Apesteguía, S. · 2021 · DOI 10.1038/s41586-021-03834-3
  6. The origin of squamates revealed by a Middle Triassic lizard from the Italian AlpsSimões, T.R.; Caldwell, M.W.; Tałanda, M.; et al. · 2018 · DOI 10.1038/s41586-018-0093-3
  7. Synchrotron tomography of a stem lizard elucidates early squamate anatomyTałanda, M.; Fernandez, V.; Panciroli, E.; Evans, S.E.; et al. · 2022 · DOI 10.1038/s41586-022-05332-6
  8. A Triassic crown squamateWhiteside, D.I.; Chambi-Trowell, S.A.V.; Benton, M.J. · 2022 · DOI 10.1126/sciadv.abq8274
  9. The affinities of the Late Triassic Cryptovaranoides and the age of crown squamatesBrownstein, C.D.; Simões, T.R.; Caldwell, M.W.; Lee, M.S.Y.; Meyer, D.L.; Scarpetta, S.G. · 2023 · DOI 10.1098/rsos.230968
  10. Late Triassic Cryptovaranoides microlanius is a squamate, not an archosauromorphWhiteside, D.I.; Chambi-Trowell, S.A.V.; Benton, M.J. · 2024 · DOI 10.1098/rsos.231874
  11. Cryptovaranoides is not a squamateCaldwell, M.W.; Brownstein, C.D.; Meyer, D.L.; Scarpetta, S.G.; Lee, M.S.Y.; Simões, T.R. · 2025 · DOI 10.7554/eLife.107021
  12. Inferring weak spots in phylogenetic trees: application to mosasauroid nomenclatureMadzia, D.; Cau, A. · 2017 · DOI 10.7717/peerj.3782
  13. Dallasaurus turneri, a new primitive mosasauroid from the Middle Turonian of Texas and comments on the phylogeny of Mosasauridae (Squamata)Bell, G.L. Jr; Polcyn, M.J. · 2005 · DOI 10.1017/S0016774600020965