Stories / 11 minSeven evidence boundaries in flowering-plant history
Compare calibration-sensitive clocks, dated whole plants, regional phytolith assemblages and animal-diet isotopes without turning them into one false origin or dominance timeline.
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 · 152 Ma · evidenceOne dataset, three clock ranges
A 2026 analysis integrates 25,685 fossil occurrences with molecular data, but its crown-angiosperm interval changes radically with calibration treatment; the narrow Late Jurassic result is the authors' preferred model, not a fossil flower.
The atlas displays the preferred hard-bound result while exposing the much older alternatives beside it.
claim:event:crown-angiosperm-calibration-sensitivity02 · 132.5 Ma · treeMajor lineages in an Early Cretaceous model
A separate metacalibrated time tree places several major flowering-plant crown lineages near 135–130 Ma. Those estimates neither validate the atlas's legacy ranges nor record fossil first appearances.
The navigation tree is an educational subset: monocots and eudicots do not exhaust Angiospermae, and Magnoliopsida is not an exact eudicot catalogue root.
claim:event:angiosperm-expansion03 · 123.5 Ma · evidenceMany specimens, one extinct habit
More than one thousand Montsechia specimens combine leafy axes, closed single-seeded fruits and depositional evidence for a submerged freshwater plant. They do not make the flowering-plant ancestor aquatic.
A fossil habit, a phylogenetic placement and an ancestral ecological state are different claims.
claim:event:barremian-montsechia04 · 124.2 Ma · evidenceA dated eudicot whole plant
Leefructus links diagnostic leaves and reproductive organs in a 125.8–122.6 Ma Yixian bed, supporting an early eudicot record while leaving Ranunculaceae affinity provisional.
One locality cannot define the global origin, first appearance or diversity of eudicots.
claim:event:yixian-leefructus05 · 115 Ma · evidenceRoots and flowers in one monocot
Cratolirion preserves roots, leaves, anatomy and reproductive organs together at about 115 Ma. Its crown-monocot placement does not turn it into a modern lily or the first monocot.
Whole-plant preservation strengthens character association, not claims beyond the analysed specimen and placement.
claim:event:crato-cratolirion06 · 6.75 Ma · evidenceA regional grass-community proxy
Fourteen Great Plains palaeosol assemblages record an 8–5.5 Ma increase in potentially C4 grass phytoliths. The 50–60% value applies within grasses, not to all vegetation.
Regional assemblages and diagnostic limits prevent a synchronous global C4-grassland claim.
claim:event:great-plains-c4-phytolith-transition07 · 7 Ma · mapAnimal diets reveal C4 biomass
Tooth-enamel carbon isotopes record widespread, regionally asynchronous C4 biomass expansion around 8–6 Ma. They do not identify the exact C4 plant lineages or directly measure open-grassland cover.
Dietary isotope proxy, plant identity, vegetation cover and faunal adaptation must remain separate.
claim:event:c4-grassland-expansionReferences
- Integrated analysis of fossils and molecular divergence time estimates a latest Jurassic origin of angiospermsWu, R.; Álvarez-Carretero, S.; Tong, Y.; Wan, S.; Schneider, H.; Clark, J.; Pisani, D.; Silvestro, D.; et al. · 2026 · DOI 10.1038/s41477-026-02311-x
- A metacalibrated time-tree documents the early rise of flowering plant phylogenetic diversityMagallón, S.; Gómez-Acevedo, S.; Sánchez-Reyes, L.L.; Hernández-Hernández, T. · 2015 · DOI 10.1111/nph.13264
- Montsechia, an ancient aquatic angiospermGomez, B.; Daviero-Gomez, V.; Coiffard, C.; Martín-Closas, C.; Dilcher, D.L. · 2015 · DOI 10.1073/pnas.1509241112
- A eudicot from the Early Cretaceous of ChinaSun, G.; Dilcher, D.L.; Wang, H.; Chen, Z. · 2011 · DOI 10.1038/nature09811
- Fossil evidence of core monocots in the Early CretaceousCoiffard, C.; Kardjilov, N.; Manke, I.; Bernardes-de-Oliveira, M.E.C. · 2019 · DOI 10.1038/s41477-019-0468-y
- The Neogene transition from C3 to C4 grasslands in North America: assemblage analysis of fossil phytolithsStrömberg, C.A.E.; McInerney, F.A. · 2011 · DOI 10.1666/09067.1
- Global vegetation change through the Miocene/Pliocene boundaryCerling, T.E.; Harris, J.M.; MacFadden, B.J.; et al. · 1997 · DOI 10.1038/38229