Evolution of stomatal responsiveness to CO2and optimization of water-use efficiency among land plants
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Elevated-CO2 Response of Stomata and Its Dependence on Environmental FactorsUsing modern plant trait relationships between observed and theoretical maximum stomatal conductance and vein density to examine patterns of plant macroevolutionOptimal allocation of leaf epidermal area for gas exchangeRapid response of leaf photosynthesis in two fern species Pteridium aquilinum and Thelypteris dentata to changes in CO2 measured by tunable diode laser absorption spectroscopyStomatal density and aperture in non-vascular land plants are non-responsive to above-ambient atmospheric CO2 concentrationsDoes low stomatal conductance or photosynthetic capacity enhance growth at elevated CO2 in Arabidopsis?The EAR motif controls the early flowering and senescence phenotype mediated by over-expression of SlERF36 and is partly responsible for changes in stomatal density and photosynthesisSeparating active and passive influences on stomatal control of transpirationEvolution of the bHLH genes involved in stomatal development: implications for the expansion of developmental complexity of stomata in land plantsSlERF36, an EAR-motif-containing ERF gene from tomato, alters stomatal density and modulates photosynthesis and growthThe origin of the sporophyte shoot in land plants: a bryological perspectiveFern and lycophyte guard cells do not respond to endogenous abscisic acidMajor transitions in the evolution of early land plants: a bryological perspectiveGlobal CO2 rise leads to reduced maximum stomatal conductance in Florida vegetationClimate forcing due to optimization of maximal leaf conductance in subtropical vegetation under rising CO2.Decline of leaf hydraulic conductance with dehydration: relationship to leaf size and venation architectureExperimental evidence for heat plume-induced cavitation and xylem deformation as a mechanism of rapid post-fire tree mortality.Acclimation of leaf cohorts expanded under light and water stresses: an adaptive mechanism of Eucryphia cordifolia to face changes in climatic conditions?The space-time continuum: the effects of elevated CO2 and temperature on trees and the importance of scaling.No evidence of general CO2 insensitivity in ferns: one stomatal control mechanism for all land plants?Sensitivity of plants to changing atmospheric CO2 concentration: from the geological past to the next century.Photosynthesis limitations in three fern species.Unique responsiveness of angiosperm stomata to elevated CO2 explained by calcium signalling.Seasonal variability of the parameters of the Ball-Berry model of stomatal conductance in maize (Zea mays L.) and sunflower (Helianthus annuus L.) under well-watered and water-stressed conditions.Fern Stomatal Responses to ABA and CO2 Depend on Species and Growth Conditions.Inferring climate from angiosperm leaf venation networks.Stomatal CO2 responsiveness and photosynthetic capacity of tropical woody species in relation to taxonomy and functional traits.Two tropical conifers show strong growth and water-use efficiency responses to altered CO2 concentrationStomatal cell wall composition: distinctive structural patterns associated with different phylogenetic groups.Physiological mechanisms drive differing foliar calcium content in ferns and angiosperms.Estimating the sensitivity of stomatal conductance to photosynthesis: a review.What are the evolutionary origins of stomatal responses to abscisic acid in land plants?Increasing atmospheric humidity and CO2 concentration alleviate forest mortality riskAncestral stomatal control results in a canalization of fern and lycophyte adaptation to drought.Augmentation of abscisic acid (ABA) levels by drought does not induce short-term stomatal sensitivity to CO2 in two divergent conifer species.Plant acclimation to elevated CO₂ affects important plant functional traits, and concomitantly reduces plant colonization rates by an herbivorous insect.Ecophysiology of four co-occurring lycophyte species: an investigation of functional convergence.Three Key Sub-leaf Modules and the Diversity of Leaf Designs.Smaller, faster stomata: scaling of stomatal size, rate of response, and stomatal conductance.Ferns are less dependent on passive dilution by cell expansion to coordinate leaf vein and stomatal spacing than angiosperms.
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P2860
Evolution of stomatal responsiveness to CO2and optimization of water-use efficiency among land plants
description
article
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im August 2009 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2009
@uk
name
Evolution of stomatal responsi ...... e efficiency among land plants
@en
Evolution of stomatal responsi ...... e efficiency among land plants
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type
label
Evolution of stomatal responsi ...... e efficiency among land plants
@en
Evolution of stomatal responsi ...... e efficiency among land plants
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prefLabel
Evolution of stomatal responsi ...... e efficiency among land plants
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Evolution of stomatal responsi ...... e efficiency among land plants
@nl
P50
P1433
P1476
Evolution of stomatal responsi ...... e efficiency among land plants
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P2093
Taylor S Feild
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P356
10.1111/J.1469-8137.2009.02844.X
P407
P577
2009-04-23T00:00:00Z