Tropospheric O3 moderates responses of temperate hardwood forests to elevated CO2: a synthesis of molecular to ecosystem results from the Aspen FACE project

By D. Karnosky, D. Zak, K. Pregitzer, C. Awmack, J. Bockheim, R. E. Dickson, G. Hendrey, G. Host, J. King, B. Kopper and 21 more. 2003

333 citations recorded by the source corpus.

Subfields: Atmospheric Science, Global and Planetary Change, Plant Science

View Paper: https://www.semanticscholar.org/paper/82ec1bebcbe3aa1d7284ccf157c4ac1ee2770f14

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Citations in the corpus

Competition increasingly dominates the responsiveness of juvenile beech and spruce to elevated CO2 and/or O3 concentrations throughout two subsequent growing seasons (2005, background): “…to O3 than deciduous trees (Skärby et al., 1998; Landolt et al., 2000), being aware, however, that the variation of genotypes within a species may strongly determine their responsiveness to O3 and their CO2 O3 interactions (Vanderheyden et al., 2001; Wustman et al., 2001; Karnosky et al., 2003).”
Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE. (2009, background): “In a similar experiment at AspenFACE with the North American plantation species, aspen (Populus tremuloides) and birch (Betula papyrifera), acclimation of photosynthesis was again not observed in the first years of the experiment, and stimulation of A was maximal (Karnosky et al., 2003).”
Altered genotypic and phenotypic frequencies of aphid populations under enriched CO2 and O3 atmospheres (2005, background): “These two genotypes also displayed marked differences in phenotypic frequencies.”
What have we learned from 15 years of free-air CO2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO2. (2004, background): “7 Mean response to elevated [CO2] of plant height, stem diameter, leaf number, leaf-area index (LAI), specific leaf area (SLA), above-ground dry matter production (DMP), and crop yield.”
CO2 enrichment and carbon partitioning to phenolics: do plant responses accord better with the protein competition or the growth differentiation balance models? (2005, methodology): “Clearly, elevated CO 2 has not yet changed the leaf surface or leaf mass allometry of aspens or birches (Karnosky et al. 2003, W. J. Mattson et al., unpubl.).”
Indirect radiative forcing of climate change through ozone effects on the land-carbon sink (2007, background): “The set of equations (4), (5) and (6) produces a quadratic in F that can be solved analytically.”
Ants, altitude and change in the northern Cape Floristic Region (2006, background): “Nevertheless, their absence in these plans and the planning processes that gave rise to them is not a consequence of lack of concern, but rather the absence of adequate information (Cowling et al., 2003).”
Functional leaf traits, plant communities and acclimation processes in relation to oxidative stress in trees: a critical overview (2008, background): “In this context, ozone is considered a factor potentially capable of reducing these ‘benefits’ (Loats & Rebbeck, 1999; Isebrands et al., 2001; Karnosky et al., 2003; King et al., 2005; Kubiske et al., 2006).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “This compensatory effect has been observed in many cases (Karnosky et al., 2003).”