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Seven 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 · evidence

One 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-sensitivity
02 · 132.5 Ma · tree

Major 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-expansion
03 · 123.5 Ma · evidence

Many 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-montsechia
04 · 124.2 Ma · evidence

A 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-leefructus
05 · 115 Ma · evidence

Roots 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-cratolirion
06 · 6.75 Ma · evidence

A 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-transition
07 · 7 Ma · map

Animal 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-expansion

References

  1. 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
  2. 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
  3. Montsechia, an ancient aquatic angiospermGomez, B.; Daviero-Gomez, V.; Coiffard, C.; Martín-Closas, C.; Dilcher, D.L. · 2015 · DOI 10.1073/pnas.1509241112
  4. A eudicot from the Early Cretaceous of ChinaSun, G.; Dilcher, D.L.; Wang, H.; Chen, Z. · 2011 · DOI 10.1038/nature09811
  5. 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
  6. 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
  7. Global vegetation change through the Miocene/Pliocene boundaryCerling, T.E.; Harris, J.M.; MacFadden, B.J.; et al. · 1997 · DOI 10.1038/38229