Why is plant-growth response to elevated CO2amplified when water is limiting, but reduced when nitrogen is limiting? A growth-optimisation hypothesis
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Evaluation of 11 terrestrial carbon-nitrogen cycle models against observations from two temperate Free-Air CO2 Enrichment studiesHow light competition between plants affects their response to climate change.Spatial variability and temporal trends in water-use efficiency of European forests.Constraints to nitrogen acquisition of terrestrial plants under elevated CO2.Global patterns and substrate-based mechanisms of the terrestrial nitrogen cycle.Trait Acclimation Mitigates Mortality Risks of Tropical Canopy Trees under Global Warming.CO2 enhancement of forest productivity constrained by limited nitrogen availability.Is analysing the nitrogen use at the plant canopy level a matter of choosing the right optimization criterion?Potential and limitations of inferring ecosystem photosynthetic capacity from leaf functional traits.Modeling carbon allocation in trees: a search for principles.Cumulative response of ecosystem carbon and nitrogen stocks to chronic CO₂ exposure in a subtropical oak woodland.On the complementary relationship between marginal nitrogen and water-use efficiencies among Pinus taeda leaves grown under ambient and CO2-enriched environments.Why does leaf nitrogen decline within tree canopies less rapidly than light? An explanation from optimization subject to a lower bound on leaf mass per area.Drought × CO2 interactions in trees: a test of the low-intercellular CO2 concentration (Ci ) mechanism.Explaining biomass growth of tropical canopy trees: the importance of sapwoodInterspecific vs intraspecific patterns in leaf nitrogen of forest trees across nitrogen availability gradients.Modeling forest stand dynamics from optimal balances of carbon and nitrogen.Effects of elevated CO2 on fine root biomass are reduced by aridity but enhanced by soil nitrogen: A global assessment.Biochar addition induced the same plant responses as elevated CO2 in mine spoil.Seasonal not annual rainfall determines grassland biomass response to carbon dioxide.Interactive Effects of CO2 Concentration and Water Regime on Stable Isotope Signatures, Nitrogen Assimilation and Growth in Sweet Pepper.Responses of Intrinsic Water-use Efficiency and Tree Growth to Climate Change in Semi-Arid Areas of North China.Whole-canopy carbon gain as a result of selection on individual performance of ten genotypes of a clonal plant.Stability of plant defensive traits among populations in two Eucalyptus species under elevated carbon dioxide.Moving beyond photosynthesis: from carbon source to sink-driven vegetation modeling.Post-fire resprouting responses of native and exotic grasses from Cumberland Plain Woodland (Sydney, Australia) under elevated carbon dioxideTraits to stay, traits to move: a review of functional traits to assess sensitivity and adaptive capacity of temperate and boreal trees to climate changeOptimal Function Explains Forest Responses to Global ChangeA trait-based ecosystem model suggests that long-term responsiveness to rising atmospheric CO2concentration is greater in slow-growing than fast-growing plantsEffects of elevated atmospheric [CO2] on instantaneous transpiration efficiency at leaf and canopy scales in Eucalyptus salignaDepth-dependency of trembling aspen and paper birch small-root responses to eCO2 and eO3Applying a SPA model to examine the impact of climate change on GPP of open woodlands and the potential for woody thickeningIs productivity of mesic savannas light limited or water limited? Results of a simulation study
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Why is plant-growth response to elevated CO2amplified when water is limiting, but reduced when nitrogen is limiting? A growth-optimisation hypothesis
description
article
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im Jahr 2008 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
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наукова стаття, опублікована у 2008
@uk
name
Why is plant-growth response t ...... growth-optimisation hypothesis
@en
Why is plant-growth response t ...... growth-optimisation hypothesis
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type
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Why is plant-growth response t ...... growth-optimisation hypothesis
@en
Why is plant-growth response t ...... growth-optimisation hypothesis
@nl
prefLabel
Why is plant-growth response t ...... growth-optimisation hypothesis
@en
Why is plant-growth response t ...... growth-optimisation hypothesis
@nl
P2093
P356
P1476
Why is plant-growth response t ...... growth-optimisation hypothesis
@en
P2093
Belinda E. Medlyn
Craig V. M. Barton
Richard J. Norby
Roderick C. Dewar
Ross E. McMurtrie
P356
10.1071/FP08128
P577
2008-01-01T00:00:00Z