The role of isohydric and anisohydric species in determining ecosystem-scale response to severe drought.

Ongoing shifts in the species composition of Eastern US forests necessitate the development of frameworks to explore how species-specific water-use strategies influence ecosystem-scale carbon (C) cycling during drought. Here, we develop a diagnostic framework to classify plant drought-response strategies along a continuum of isohydric to anisohydric regulation of leaf water potential (Ψ(L)). The framework is applied to a 3-year record of weekly leaf-level gas exchange and Ψ measurements collected in the Morgan-Monroe State Forest (Indiana, USA), where continuous observations of the net ecosystem exchange of CO2 (NEE) have been ongoing since 1999. A severe drought that occurred in the middle of the study period reduced the absolute magnitude of NEE by 55%, though species-specific responses to drought conditions varied. Oak species were characterized by anisohydric regulation of Ψ(L) that promoted static gas exchange throughout the study period. In contrast, Ψ(L) of the other canopy dominant species was more isohydric, which limited gas exchange during the drought. Ecosystem-scale estimates of NEE and gross ecosystem productivity derived by upscaling the leaf-level data agreed well with tower-based observations, and highlight how the fraction of isohydric and anisohydric species in forests can mediate net ecosystem C balance.

Increased resin flow in mature pine trees growing under elevated CO2 and moderate soil fertility.

Warmer climates induced by elevated atmospheric CO(2) (eCO(2)) are expected to increase damaging bark beetle activity in pine forests, yet the effect of eCO(2) on resin production--the tree's primary defense against beetle attack--remains largely unknown. Following growth-differentiation balance theory, if extra carbohydrates produced under eCO(2) are not consumed by respiration or growth, resin production could increase. Here, the effect of eCO(2) on resin production of mature pines is assessed. As predicted, eCO(2) enhanced resin flow by an average of 140% (P=0.03) in canopy dominants growing in low-nitrogen soils, but did not affect resin flow in faster-growing fertilized canopy dominants or in carbohydrate-limited suppressed individuals. Thus, pine trees may become increasingly protected from bark beetle attacks in an eCO(2) climate, except where they are fertilized or are allowed to become overcrowded.

Carbon dioxide and water vapor exchange in a warm temperate grassland.

Grasslands cover about 40% of the ice-free global terrestrial surface, but their contribution to local and regional water and carbon fluxes and sensitivity to climatic perturbations such as drought remains uncertain. Here, we assess the direction and magnitude of net ecosystem carbon exchange (NEE) and its components, ecosystem carbon assimilation ( A(c)) and ecosystem respiration ( R(E)), in a southeastern United States grassland ecosystem subject to periodic drought and harvest using a combination of eddy-covariance measurements and model calculations. We modeled A(c) and evapotranspiration (ET) using a big-leaf canopy scheme in conjunction with ecophysiological and radiative transfer principles, and applied the model to assess the sensitivity of NEE and ET to soil moisture dynamics and rapid excursions in leaf area index (LAI) following grass harvesting. Model results closely match eddy-covariance flux estimations on daily, and longer, time steps. Both model calculations and eddy-covariance estimates suggest that the grassland became a net source of carbon to the atmosphere immediately following the harvest, but a rapid recovery in LAI maintained a marginal carbon sink during summer. However, when integrated over the year, this grassland ecosystem was a net C source (97 g C m(-2) a(-1)) due to a minor imbalance between large A(c) (-1,202 g C m(-2) a(-1)) and R(E) (1,299 g C m(-2) a(-1)) fluxes. Mild drought conditions during the measurement period resulted in many instances of low soil moisture (theta<0.2 m(3)m(-3)), which influenced A(c) and thereby NEE by decreasing stomatal conductance. For this experiment, low theta had minor impact on R(E). Thus, stomatal limitations to A(c) were the primary reason that this grassland was a net C source. In the absence of soil moisture limitations, model calculations suggest a net C sink of -65 g C m(-2) a(-1) assuming the LAI dynamics and physiological properties are unaltered. These results, and the results of other studies, suggest that perturbations to the hydrologic cycle are key determinants of C cycling in grassland ecosystems.