| Q57915241 | A 450-Million-Year History of Fire |
| Q64101310 | ASYMMETRIC LEAVES1 and REVOLUTA are the key regulatory genes associated with pitcher development in Nepenthes khasiana |
| Q37799688 | Ancient Atmospheres and the Evolution of Oxygen Sensing Via the Hypoxia-Inducible Factor in Metazoans |
| Q47149082 | Ancient cell structural traits and photosynthesis in today’s environment. |
| Q28770177 | Biophysical constraints on the origin of leaves inferred from the fossil record |
| Q35036782 | Carbon metabolite feedback regulation of leaf photosynthesis and development |
| Q47203661 | Contrasting arbuscular mycorrhizal responses of vascular and non-vascular plants to a simulated Palaeozoic CO₂ decline |
| Q41690795 | Differences in the photosynthetic plasticity of ferns and Ginkgo grown in experimentally controlled low [O₂]:[CO₂] atmospheres may explain their contrasting ecological fate across the Triassic–Jurassic mass extinction boundary |
| Q44593448 | Do drought-hardened plants suffer from fever? |
| Q46321171 | Enhancing (crop) plant photosynthesis by introducing novel genetic diversity. |
| Q46256173 | Evolution and ecology of plant architecture: integrating insights from the fossil record, extant morphology, developmental genetics and phylogenies. |
| Q28740619 | Evolution of C4 plants: a new hypothesis for an interaction of CO2 and water relations mediated by plant hydraulics |
| Q29999879 | Evolution of developmental potential and the multiple independent origins of leaves in Paleozoic vascular plants |
| Q56058899 | Evolution of the life cycle in land plants |
| Q37767954 | Evolution of tree nutrition |
| Q27003923 | Evolutionary context for understanding and manipulating plant responses to past, present and future atmospheric [CO2 |
| Q28682076 | Evolutionary relationship and structural characterization of the EPF/EPFL gene family |
| Q46911441 | Expanding knowledge of the Rubisco kinetics variability in plant species: environmental and evolutionary trends. |
| Q46282868 | Extending the scope of Darwin's 'abominable mystery': integrative approaches to understanding angiosperm origins and species richness |
| Q30662330 | From milliseconds to millions of years: guard cells and environmental responses |
| Q39010778 | Higher rates of leaf gas exchange are associated with higher leaf hydrodynamic pressure gradients |
| Q89088050 | Hornwort stomata do not respond actively to exogenous and environmental cues |
| Q90040445 | IBR5 Regulates Leaf Serrations Development via Modulation of the Expression of PIN1 |
| Q52929209 | Impaired photosynthesis and increased leaf construction costs may induce floral stress during episodes of global warming over macroevolutionary timescales. |
| Q34487465 | Land plants equilibrate O2 and CO2 concentrations in the atmosphere. |
| Q28653100 | Leaf energy balance modelling as a tool to infer habitat preference in the early angiosperms |
| Q28607356 | Leaf evolution in early-diverging ferns: insights from a new fern-like plant from the Late Devonian of China |
| Q28651122 | Leaf evolution: gases, genes and geochemistry |
| Q28727726 | Leaf fossil record suggests limited influence of atmospheric CO2 on terrestrial productivity prior to angiosperm evolution |
| Q38100205 | Leaf venation: structure, function, development, evolution, ecology and applications in the past, present and future |
| Q46943182 | Light-dependent reversible phosphorylation of the minor photosystem II antenna Lhcb6 (CP24) occurs in lycophytes |
| Q28740617 | Megacycles of atmospheric carbon dioxide concentration correlate with fossil plant genome size |
| Q28740621 | Morphological evolution in land plants: new designs with old genes |
| Q50045746 | On plant growth and form |
| Q47632962 | Palaeontology. Turning over a new leaf |
| Q56113887 | Plant breeding and climate changes |
| Q37788795 | Plant responses to low [CO2] of the past |
| Q28680722 | Plant water use efficiency over geological time--evolution of leaf stomata configurations affecting plant gas exchange |
| Q58071141 | Reading a CO2 signal from fossil stomata |
| Q56554517 | Reinvestigation of the Late Devonian Shougangia bella and new insights into the evolution of fern-like plants |
| Q34560915 | Sensitivity of plants to changing atmospheric CO2 concentration: from the geological past to the next century. |
| Q33349585 | Signaling sides adaxial-abaxial patterning in leaves |
| Q64236085 | Significance of Photosynthetic Characters in the Evolution of Asian (Gnetales) |
| Q57030067 | Stepwise oxygenation of the Paleozoic atmosphere |
| Q38980664 | Stomatal cell wall composition: distinctive structural patterns associated with different phylogenetic groups |
| Q34566492 | Stomatal control and leaf thermal and hydraulic capacitances under rapid environmental fluctuations |
| Q57703614 | Stomatal control as a driver of plant evolution |
| Q28649304 | Stomatal density and aperture in non-vascular land plants are non-responsive to above-ambient atmospheric CO2 concentrations |
| Q35625700 | The Arabidopsis circadian system. |
| Q41889036 | The Huperzia selago Shoot Tip Transcriptome Sheds New Light on the Evolution of Leaves |
| Q34244519 | The evolutionary history of maternal plant-manipulation and larval feeding behaviours in attelabid weevils (Coleoptera; Curculionoidea). |
| Q46237177 | The origin and early evolution of vascular plant shoots and leaves. |
| Q29393342 | The origin of herbivory on land: Initial patterns of plant tissue consumption by arthropods |
| Q33860173 | Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress. |
| Q33359861 | What determines a leaf's shape? |
| Q90055207 | Why Are There so Many Plant Species That Transiently Flush Young Leaves Red in the Tropics? |
| Q35866752 | Why should we investigate the morphological disparity of plant clades? |