Abstract

Anatomical and physiological acclimation to water stress of the tree hydraulic system involves trade-offs between maintenance of stomatal conductance and loss of hydraulic conductivity, with short-term impacts on photosynthesis and long-term consequences to survival and growth. Here, we study the role of variations in root and branch maximum hydraulic specific conductivity (ks-max) under high and low soil moisture in determining whole-tree hydraulic conductance (Ktree) and in mediating stomatal control of gas exchange in four contrasting tree species growing under ambient and elevated CO2 (CO2a and CO2e). We hypothesized that Ktree would adjust to CO2e through an increase in root and branch ks-max in response to anatomical adjustments. However, physiological changes observed under CO2e were not clearly related to structural change in the xylem of any of the species. The only large effect of CO2e occurred in branches of Liquidambar styraciflua L. and Cornus florida L. where an increase in ks-max and a decrease in xylem resistance to embolism (−P50) were measured. Across species, embolism in roots explained the loss of Ktree and therefore indirectly constituted a hydraulic signal involved in stomatal regulation and in the reduction of Gs-ref, the sap-flux-scaled mean canopy stomatal conductance at a reference vapour pressure deficit of 1 kPa. Across roots and branches, the increase in ks-max was associated with a decrease in −P50, a consequence of structural acclimation such as larger conduits, lower pit resistance and lower wood density. Across species, treatment-induced changes in Ktree translated to similar variation in Gs-ref. However, the relationship between Gs-ref and Ktree under CO2a was steeper than under CO2e, indicating that CO2e trees have lower Gs-ref at a given Ktree than CO2a trees. Under high soil moisture, CO2e greatly reduced Gs-ref. Under low soil moisture, CO2e reduced Gs-ref of only L. styraciflua and Ulmus alata. In some species, higher xylem dysfunction under CO2e might impact tree performance in a future climate when increased evaporative demand could cause a greater loss of hydraulic function. The results contributed to our knowledge of the physiological and anatomical mechanisms underpinning the responses of tree species to drought and more generally to global change.

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