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Thirteen dossiers across molluscan and brachiopod body plans

Move from named fossils to living genomes and experiments while keeping observation, homology, topology and nomenclature separate.

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 · 556.5 Ma · evidence

A body outline remains mollusc-like, not crown-defined

More than 35 White Sea specimens preserve bilateral organization and a dorsal cover, but no radula or crown-mollusc diagnosis.

A named Ediacaran sample tests character homology without becoming a direct ancestor or global Mollusca first appearance.

claim:event:kimberella-white-sea-morphology
02 · 506.5 Ma · evidence

Repeated tooth rows make a radula testable

Across 189 Odontogriphus specimens, paired teeth on a membrane show posterior replacement beside a broad foot and mantle groove.

The geometry is observed; radular homology and stem-mollusc placement remain comparative conclusions.

claim:event:odontogriphus-radula-sample
03 · 506.5 Ma · tree

A shell and sclerites occur in one articulated body

Orthrozanclus combines an anterior shell, three zones of imbricating sclerites and long marginal spines.

Halwaxiida is a scored topology, not an observed ancestor chain or secure crown assignment.

claim:event:orthrozanclus-halwaxiid-mosaic
04 · 517 Ma · evidence

Shell sections separate laminae from nacre

Pojetaia sections preserve a laminar inner fabric compared with foliated aragonite; undisputed Cambrian nacre is withheld.

Preservation and homology limit mineral interpretation; the sections do not establish every bivalve shell pathway.

claim:event:pojetaia-shell-microstructure
05 · 506.5 Ma · tree

A soft body tests a difficult cephalopod hypothesis

Nectocaris has paired eyes, fins, two tentacles and a funnel-like structure in ninety newly prepared specimens.

Missing shell, siphuncle, beak and radula evidence keeps the cephalopod placement explicitly contested.

claim:event:nectocaris-soft-body-cephalopod-test
06 · 0 Ma · tree

One phylogenomic matrix recovers Aculifera

Chitons group with sampled aplacophorans, while gastropods and bivalves form another supported clade in the Kocot et al. analyses.

Monoplacophora was absent and some alternatives were not rejected, so the result remains matrix-specific.

claim:event:aculifera-phylogenomic-topology
07 · 0 Ma · tree

A second matrix adds every major living group

Fifteen new transcriptomes bring Monoplacophora into an all-class sample that recovers it with Cephalopoda in principal analyses.

Conflicting deep nodes and corrected supplementary figures are retained rather than averaged into false certainty.

claim:event:all-class-mollusc-phylogenomics
08 · 0 Ma · evidence

Embryos connect Nodal to shell chirality

Lottia and Biomphalaria express nodal and Pitx on opposite sides; inhibition disrupts pathway output and shell coiling.

This living experiment does not directly reconstruct fossil torsion or every gastropod coiling mechanism.

claim:event:gastropod-nodal-chirality
09 · 0 Ma · evidence

A genome tests cephalopod novelty without duplication

One Octopus bimaculoides genome and twelve tissue transcriptomes reveal targeted family expansions and extensive rearrangement.

Comparative association is not a single-gene cause of arms, suckers or neural complexity; whole-genome duplication was not supported.

claim:event:octopus-genome-innovation
10 · 525 Ma · evidence

Two isolated sclerite types build a falsifiable model

Micrina mitral and sellate sclerites have complementary geometry and muscle scars used to reconstruct a sessile bivalved animal.

Articulation and valve homology are reconstructions, not a preserved whole organism or settled stem topology.

claim:event:micrina-bivalved-reconstruction
11 · 519 Ma · evidence

A calcareous brachiopod preserves soft anatomy

Kutorgina chengjiangensis preserves an early spirolophe, digestive tract and pedicle within paired valves.

Direct anatomy informs comparison but does not make Kutorgina the ancestor of living rhynchonelliformeans.

claim:event:kutorgina-soft-tissue-anatomy
12 · 0 Ma · evidence

A living brachiopod shell is tested across three data layers

The Lingula genome, staged transcriptomes and shell proteome separate shared components from lineage-specific phosphate-shell proteins.

Shared genes do not imply shell identity, vertebrate bone homology or morphological stasis through the fossil record.

claim:event:lingula-genome-biomineralization
13 · 519 Ma · tree

A tube, valves and lophophore resist a simple ladder

Yuganotheca combines paired agglutinated valves, a horseshoe lophophore, a bipartite tube and a long pedicle.

COL26.8 routes 159,801 accepted living names here; that naming coverage cannot resolve this fossil mosaic or turn thirteen dossiers into an ancestor series.

claim:event:yuganotheca-tubular-lophophorate

References

  1. The Late Precambrian fossil Kimberella is a mollusc-like bilaterian organismFedonkin, M.A.; Waggoner, B.M. · 1997 · DOI 10.1038/42242
  2. A soft-bodied mollusc with radula from the Middle Cambrian Burgess ShaleCaron, J.-B.; Scheltema, A.; Schander, C.; Rudkin, D. · 2006 · DOI 10.1038/nature04894
  3. Halwaxiids and the early evolution of the lophotrochozoansConway Morris, S.; Caron, J.-B. · 2007 · DOI 10.1126/science.1137187
  4. Shell microstructure of the early bivalve Pojetaia and the independent origin of nacre within the MolluscaVendrasco, M.J.; Checa, A.G.; Kouchinsky, A.V. · 2011 · DOI 10.1111/j.1475-4983.2011.01056.x
  5. Primitive soft-bodied cephalopods from the CambrianSmith, M.R.; Caron, J.-B. · 2010 · DOI 10.1038/nature09068
  6. Phylogenomics reveals deep molluscan relationshipsKocot, K.M.; Cannon, J.T.; Todt, C.; Citarella, M.R.; Kohn, A.B.; Meyer, A.; Santos, S.R.; Schander, C.; Moroz, L.L.; Lieb, B.; Halanych, K.M. · 2011 · DOI 10.1038/nature10382
  7. Resolving the evolutionary relationships of molluscs with phylogenomic toolsSmith, S.A.; Wilson, N.G.; Goetz, F.E.; Feehery, C.; Andrade, S.C.S.; Rouse, G.W.; Giribet, G.; Dunn, C.W. · 2011 · DOI 10.1038/nature10526
  8. Nodal signalling is involved in left–right asymmetry in snailsGrande, C.; Patel, N.H. · 2009 · DOI 10.1038/nature07603
  9. The octopus genome and the evolution of cephalopod neural and morphological noveltiesAlbertin, C.B.; Simakov, O.; Mitros, T.; Wang, Z.Y.; Pungor, J.R.; Edsinger-Gonzales, E.; Brenner, S.; Ragsdale, C.W.; Rokhsar, D.S. · 2015 · DOI 10.1038/nature14668
  10. The Early Cambrian tommotiid Micrina, a sessile bivalved stem group brachiopodHolmer, L.E.; Skovsted, C.B.; Brock, G.A.; Valentine, J.L.; Paterson, J.R. · 2008 · DOI 10.1098/rsbl.2008.0277
  11. Rhynchonelliformean brachiopods with soft-tissue preservation from the Early Cambrian Chengjiang Lagerstätte of South ChinaZhang, Z.; Shu, D.; Emig, C.; Zhang, X.; Han, J.; Liu, J.; Li, Y.; Guo, J. · 2007 · DOI 10.1111/j.1475-4983.2007.00725.x
  12. The Lingula genome provides insights into brachiopod evolution and the origin of phosphate biomineralizationLuo, Y.-J.; Takeuchi, T.; Koyanagi, R.; Yamada, L.; Kanda, M.; Khalturina, M.; Fujie, M.; Yamasaki, S.; Endo, K.; Satoh, N. et al. · 2015 · DOI 10.1038/ncomms9301
  13. An early Cambrian agglutinated tubular lophophorate with brachiopod charactersZhang, Z.F.; Li, G.X.; Holmer, L.E.; Brock, G.A.; Balthasar, U.; Skovsted, C.B.; Fu, D.J.; Zhang, X.L.; Wang, H.Z.; Butler, A. et al. · 2014 · DOI 10.1038/srep04682