EVO ATLASEN中文
Atlas home / Stories / Thirteen dossiers from Cambrian mandibles to insect genomes
Stories / 22 min

Thirteen dossiers from Cambrian mandibles to insect genomes

Follow named fossils, transcriptome matrices, clock models and gene knockouts without turning Pancrustacea, terrestrialization or flight into a single 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 · 508 Ma · evidence

A Burgess Shale body exposes early mandibles

Holotype ROM 63823 and paratype ROM 63824 preserve the appendage combinations scored in the published matrix.

Stem-mandibulate placement is a matrix result; Tokummia is neither a demonstrated direct ancestor nor a crown crustacean, insect or myriapod.

claim:event:tokummia-mandibulate-anatomy
02 · 508 Ma · evidence

A specimen series replaces one idealized Waptia

ROMIP 56432 figures mandibles and maxillules, while ROMIP 64294 exposes disarticulated opposing mandibles within the larger specimen series.

Pancrustacean placement and active swimming predation are topology and functional interpretations, not stomach contents, observed behaviour or a direct ancestor claim.

claim:event:waptia-mandibulate-series
03 · 518 Ma · evidence

Tiny phosphatized bodies preserve growth stages

The topotype series preserves multiple developmental stages, including an eight-thoracomere stage reconstructed from phosphatized soft-part anatomy.

Eucrustacean crown placement and epipodite homology depend on character interpretation and must not be converted into an exact crown-origin date.

claim:event:yicaris-developmental-series
04 · 0 Ma · tree

Nine transcriptomes test an undersampled branch

Nine new 454 transcriptomes were combined with morphology, fossils, ESTs, genomes, mitochondrial proteins and ribosomal data.

Ostracod monophyly and several deep nodes change when fast genes, distant outgroups or data partitions change; no displayed branch is a fossil observation.

claim:event:ostracod-phylotranscriptome-topology
05 · 0 Ma · tree

Expanded remipede sampling tests the hexapod sister

Expanded remipede sampling repeatedly recovers Remipedia plus Hexapoda while supporting several major pancrustacean clades across methods.

Copepod, cephalocarid and other deep positions remain method- and sampling-sensitive, so the tree is a tested hypothesis rather than a fixed ancestor ladder.

claim:event:pancrustacea-remipede-phylogenomics
06 · 0 Ma · tree

Seven added taxa can reorganize deep branches

The final 105-taxon matrix includes 90 transcriptomes, 15 genomes and 576 protein-coding genes, compared with a 98-taxon alternative assembled through the same pipeline.

Rejected and recovered clades differ among sampled matrices and models; divergence estimates use thirteen vetted calibrations but remain clock outputs.

claim:event:pancrustacea-taxon-sampling-sensitivity
07 · 409 Ma · evidence

A Devonian abdomen preserves a springtail-like furcula

Four head capsules and about ten later body specimens include the first reported intact abdomen and a furcula comparable to living springtails.

This sampled occurrence supports collembolan affinity but does not by itself date hexapod terrestrialization, global origin or ecological dominance.

claim:event:rhyniella-springtail-material
08 · 409 Ma · evidence

One head fragment supports incompatible identities

NHMUK PI IN 38234 preserves an isolated head fragment whose mandibles were interpreted in 2004 as dicondylic and possibly pterygote-like.

Three-dimensional reanalysis in 2017 found the structures more compatible with a myriapod, possibly a scutigeromorph centipede; insect and flight calibrations are therefore contested.

claim:event:rhyniognatha-contested-affinity
09 · 0 Ma · map

Genes and fossils compare routes onto land

The core dataset contains 57 taxa and 246 genes, with fossil calibrations and a 30-species panarthropod subset used for topology tests.

A favoured marine route and inferred dates are model outputs conditioned on topology, calibrations and ancestral-state coding, not observed migrations.

claim:event:arthropod-terrestrialization-clock
10 · 324 Ma · evidence

A crushed wing anchors one Carboniferous occurrence

The approximately 10 mm crushed forewing fragment preserves cross-veins and branches of ScP, R and other main veins in lowermost Namurian strata.

Archaeorthopteran affinity follows incomplete venation, and one fragment cannot date the acquisition of powered flight or the global Pterygota first appearance.

claim:event:paskov-carboniferous-wing
11 · 0 Ma · evidence

Gene knockouts test a wing-homology model

CRISPR perturbations and expression domains compare proximal leg segments in Parhyale with cricket and other insect body-wall and wing structures.

Developmental correspondence supports a homology model but does not preserve the first wing, its ecology or one uniquely identified fossil precursor.

claim:event:parhyale-wing-homology-knockout
12 · 0 Ma · tree

A 1,478-gene matrix times sampled insect branches

The study samples 144 species, 1,478 protein-coding genes and archived transcriptomes under BioProject PRJNA183205.

Topology and node ages depend on sampling, orthology, sequence models, fossil assignments and clock priors; they are not observed fossil first appearances.

claim:event:insect-1kite-topology-clock
13 · 307 Ma · evidence

Five small fossils broaden the Carboniferous sample

The described sample includes a stem coleopterid, a holometabolous larva, a stem hymenopterid, an early hemipteran and an early psocodean.

The specimens do not demonstrate synchronous origins, exact crown-order first appearances or a single climatic cause for later diversification. COL26.8 routes 1,049,133 accepted living species names through crustaceans-insects; this is nomenclatural coverage, not 1,049,133 evidence dossiers or a phylogenomic consensus.

claim:event:pennsylvanian-eumetabola-sample

References

  1. Burgess Shale fossils illustrate the origin of the mandibulate body planAria, C.; Caron, J.-B. · 2017 · DOI 10.1038/nature22080
  2. Waptia fieldensis Walcott, a mandibulate arthropod from the middle Cambrian Burgess ShaleVannier, J.; Aria, C.; Taylor, R.S.; Caron, J.-B. · 2018 · DOI 10.1098/rsos.172206
  3. An epipodite-bearing crown-group crustacean from the Lower CambrianZhang, X.-G.; Siveter, D.J.; Waloszek, D.; Maas, A. · 2007 · DOI 10.1038/nature06138
  4. Phylotranscriptomics to Bring the Understudied into the Fold: Monophyletic Ostracoda, Fossil Placement, and Pancrustacean PhylogenyOakley, T.H.; Wolfe, J.M.; Lindgren, A.R.; Zaharoff, A.K. · 2013 · DOI 10.1093/molbev/mss216
  5. Pancrustacean Evolution Illuminated by Taxon-Rich Genomic-Scale Data Sets with an Expanded Remipede SamplingLozano-Fernandez, J.; Giacomelli, M.; Fleming, J.F.; Chen, A.; Vinther, J.; Thomsen, P.F.; Glenner, H.; Palero, F.; Legg, D.A.; Iliffe, T.M.; Pisani, D.; Olesen, J. · 2019 · DOI 10.1093/gbe/evz097
  6. Major Revisions in Pancrustacean Phylogeny and Evidence of Sensitivity to Taxon SamplingBernot, J.P.; Owen, C.L.; Wolfe, J.M.; Meland, K.; Olesen, J.; Crandall, K.A. · 2023 · DOI 10.1093/molbev/msad175
  7. A new assessment of Rhyniella, the earliest known insect, from the Devonian of Rhynie, ScotlandWhalley, P.; Jarzembowski, E.A. · 1981 · DOI 10.1038/291317a0
  8. New light shed on the oldest insectEngel, M.S.; Grimaldi, D.A. · 2004 · DOI 10.1038/nature02291
  9. The presumed oldest flying insect: more likely a myriapod?Haug, C.; Haug, J.T. · 2017 · DOI 10.7717/peerj.3402
  10. A molecular palaeobiological exploration of arthropod terrestrializationLozano-Fernandez, J.; Carton, R.; Tanner, A.R.; Puttick, M.N.; Blaxter, M.; Vinther, J.; Olesen, J.; Giribet, G.; Edgecombe, G.D.; Pisani, D. · 2016 · DOI 10.1098/rstb.2015.0133
  11. Discovery of the oldest known Pterygota in the Lower Carboniferous of the Upper Silesian Basin in the Czech Republic (Insecta: Archaeorthoptera)Prokop, J.; Nel, A.; Hoch, I. · 2005 · DOI 10.1016/j.geobios.2003.11.006
  12. Knockout of crustacean leg patterning genes suggests that insect wings and body walls evolved from ancient leg segmentsBruce, H.S.; Patel, N.H. · 2020 · DOI 10.1038/s41559-020-01349-0
  13. Phylogenomics resolves the timing and pattern of insect evolutionMisof, B.; Liu, S.; Meusemann, K.; Peters, R.S.; Donath, A.; Frandsen, P.B.; et al. · 2014 · DOI 10.1126/science.1257570
  14. The earliest known holometabolous insectsNel, A.; Roques, P.; Nel, P.; Prokin, A.A.; Bourgoin, T.; Prokop, J.; et al. · 2013 · DOI 10.1038/nature12629