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Global Change Biology · 2008 · Vol. 14 · Issue 6 · Wiley
Vegetation plays a central role in controlling terrestrial carbon (C) exchange, but quantifying its impacts on C cycling on time scales of ecological succession is hindered by a lack of long‐term observations. The net ecosystem exchange of carbon (NEE) was measured for several years in adjacent ecosystems that represent distinct phases of ecological succession in the southeastern USA. The experiment was designed to isolate the...
Global Change Biology · 2008 · Vol. 14 · Issue 3 · Wiley
Efforts to characterize carbon (C) cycling among atmosphere, forest canopy, and soil C pools are hindered by poorly quantified fine root dynamics. We characterized the influence of free‐air‐CO 2 ‐enrichment (ambient +200 ppm) on fine roots for a period of 6 years (Autumn 1998 through Autumn 2004) in an 18‐year‐old loblolly pine ( Pinus taeda ) plantation near Durham, NC, USA using minirhizotrons. Root production and mortality...
Global Change Biology · 2007 · Vol. 13 · Issue 12 · Wiley
Increased canopy leaf area ( L ) may lead to higher forest productivity and alter processes such as species dynamics and ecosystem mass and energy fluxes. Few CO 2 enrichment studies have been conducted in closed canopy forests and none have shown a sustained enhancement of L . We reconstructed 8 years (1996–2003) of L at Duke's Free Air CO 2 Enrichment experiment to determine the effects of elevated atmospheric CO 2 concentra...
Global Change Biology · 2007 · Vol. 13 · Issue 4 · Wiley
Triggers of summertime convective rainfall depend on numerous interactions and feedbacks, often compounded by spatial variability in soil moisture and its impacts on vegetation function, vegetation composition, terrain, and all the complex turbulent entrainment processes near the capping inversion. To progress even within the most restricted and idealized framework, many of the governing processes must be simplified and parame...
Global Change Biology · 2006 · Vol. 12 · Issue 11 · Wiley
We combined Eddy‐covariance measurements with a linear perturbation analysis to isolate the relative contribution of physical and biological drivers on evapotranspiration (ET) in three ecosystems representing two end‐members and an intermediate stage of a successional gradient in the southeastern US (SE). The study ecosystems, an abandoned agricultural field [old field (OF)], an early successional planted pine forest (PP), and...
Global Change Biology · 2006 · Vol. 12 · Issue 5 · Wiley
Above forest canopies, eddy covariance (EC) measurements of mass (CO 2 , H 2 O vapor) and energy exchange, assumed to represent ecosystem fluxes, are commonly made at one point in the roughness sublayer (RSL). A spatial variability experiment, in which EC measurements were made from six towers within the RSL in a uniform pine plantation, quantified large and dynamic spatial variation in fluxes. The spatial coefficient of varia...
Global Change Biology · 2003 · Vol. 9 · Issue 10 · Wiley
We linked a leaf‐level CO 2 assimilation model with a model that accounts for light attenuation in the canopy and measurements of sap‐flux‐based canopy conductance into a new canopy conductance‐constrained carbon assimilation (4C‐A) model. We estimated canopy CO 2 uptake ( A nC ) at the Duke Forest free‐air CO 2 enrichment (FACE) study. Rates of A nC estimated from the 4C‐A model agreed well with leaf gas exchange measurements...
Global Change Biology · 2003 · Vol. 9 · Issue 6 · Wiley
Elevated atmospheric carbon dioxide (CO 2 e ) increases soil respiration rates in forest, grassland, agricultural and wetland systems as a result of increased growth, root biomass and enhanced biological activity of soil microorganisms. Less is known about how forest floor fluxes respond to the combined effects of elevated CO 2 and nutrient amendments; until now no experiments have been in place with large forest trees to allo...
Global Change Biology · 2002 · Vol. 8 · Issue 9 · Wiley
Increasing atmospheric CO 2 concentration decreases stomatal conductance in many species, but the savings of water from reduced transpiration may permit the forest to retain greater leaf area index ( L ). Therefore, the net effect on water use in forest ecosystems under a higher CO 2 atmosphere is difficult to predict. The free air CO 2 enrichment (FACE) facility ( n = 3) in a 14‐m tall (in 1996) Pinus taeda L. stand was desig...
Global Change Biology · 2002 · Vol. 8 · Issue 2 · Wiley
One of the main challenges to quantifying ecosystem carbon budgets is properly quantifying the magnitude of night‐time ecosystem respiration. Inverse Lagrangian dispersion analysis provides a promising approach to addressing such a problem when measured mean CO 2 concentration profiles and nocturnal velocity statistics are available. An inverse method, termed ‘Constrained Source Optimization’ or CSO, which couples a localized...