Nocturnal fluxes may be a significant factor in the annual water budget of forested ecosystems. Here, we assessed sap flow in two co-occurring evergreen species (Eucalyptus parramattensis and Angophora bakeri) in a temperate woodland for 2 years in order to quantify the magnitude of seasonal nocturnal sap flow (E(n)) under different environmental conditions. The two species showed different diurnal water relations, demonstrated by different diurnal curves of stomatal conductance, sap flow and leaf water potential. The relative influence of several microclimatic variables, including wind speed (U), vapour pressure deficit (D), the product of U and D (UD) and soil moisture content, were quantified. D exerted the strongest influence on E(n) (r² = 0.59-0.86), soil moisture content influenced E(n) when D was constant, but U and UD did not generally influence E(n). In both species, cuticular conductance (G(c)) was a small proportion of total leaf conductance (G(s)) and was not a major pathway for E(n). We found that E(n) was primarily a function of transpiration from the canopy rather than refilling of stem storage, with canopy transpiration accounting for 50-70% of nocturnal flows. Mean E(n) was 6-8% of the 24-h flux across seasons (spring, summer and winter), but was up to 19% of the 24-h flux on some days in both species. Despite different daytime strategies in water use of the two species, both species demonstrated low night-time water loss, suggesting similar controls on water loss at night. In order to account for the impact of E(n) on pre-dawn leaf water potential arising from the influence of disequilibria between root zone and leaf water potential, we also developed a simple model to more accurately predict soil water potential (ψ(s)).

A soil–plant–atmosphere model was used to estimate gross primary productivity (GPP) and evapotranspiration (ET) of a tropical savanna in Australia. This paper describes model modifications required to simulate the substantial C4 grass understory together with C3 trees. The model was further improved to include a seasonal distribution of leaf area and foliar nitrogen through 10 canopy layers. Model outputs were compared with a 5‐year eddy covariance dataset. Adding the C4 photosynthesis component improved the model efficiency and root‐mean‐squared error (RMSE) for total ecosystem GPP by better emulating annual peaks and troughs in GPP across wet and dry seasons. The C4 photosynthesis component had minimal impact on modelled values of ET. Outputs of GPP from the modified model agreed well with measured values, explaining between 79% and 90% of the variance and having a low RMSE (0.003–0.281 g C m−2 day−1). Approximately, 40% of total annual GPP was contributed by C4 grasses. Total (trees and grasses) wet season GPP was approximately 75–80% of total annual GPP. Light‐use efficiency (LUE) was largest for the wet season and smallest in the dry season and C4 LUE was larger than that of the trees. A sensitivity analysis of GPP revealed that daily GPP was most sensitive to changes in leaf area index (LAI) and foliar nitrogen (Nf) and relatively insensitive to changes in maximum carboxylation rate (Vcmax), maximum electron transport rate (Jmax) and minimum leaf water potential (ψmin). The modified model was also able to represent daily and seasonal patterns in ET, (explaining 68–81% of variance) with a low RMSE (0.038–0.19 mm day−1). Current values of Nf, LAI and other parameters appear to be colimiting for maximizing GPP. By manipulating LAI and soil moisture content inputs, we show that modelled GPP is limited by light interception rather than water availability at this site.

Daily and seasonal patterns of tree water use were measured for the two dominant tree species, Angophora bakeri E.C.Hall (narrow-leaved apple) and Eucalyptus sclerophylla (Blakely) L.A.S. Johnson & Blaxell (scribbly gum), in a temperate, open, evergreen woodland using sap flow sensors, along with information about soil, leaf, tree and micro-climatological variables. The aims of this work were to: (a) validate a soil–plant–atmosphere (SPA) model for the specific site; (b) determine the total depth from which water uptake must occur to achieve the observed rates of tree sap flow; (c) examine whether the water content of the upper soil profile was a significant determinant of daily rates of sap flow; and (d) examine the sensitivity of sap flow to several biotic factors. It was found that: (a) the SPA model was able to accurately replicate the hourly, daily and seasonal patterns of sap flow; (b) water uptake must have occurred from depths of up to 3 m; (c) sap flow was independent of the water content of the top 80 cm of the soil profile; and (d) sap flow was very sensitive to the leaf area of the stand, whole tree hydraulic conductance and the critical water potential of the leaves, but insensitive to stem capacitance and increases in root biomass. These results are important to future studies of the regulation of vegetation water use, landscape-scale behaviour of vegetation, and to water resource managers, because they allow testing of large-scale management options without the need for large-scale manipulations of vegetation cover.

script developed incorporates a function to connect directly a digital camera, or high 6 resolution webcam, from a laptop to obtain cover photographs and LAI analysis in 7 real time. The later is a novel feature which is not available on commercial LAI 8 analysis softwares for cover photography. This script is available for interested 9 researchers. 10 11

Stomata respond to increasing leaf-to-air vapour pressure difference (LAVPD) (D) by closing. The mechanism by which this occurs is debated. A role for feedback and peristomatal transpiration has been proposed. In this paper, we apply a recent mechanistic model of stomatal behaviour, and compare model and experimental data for the influence of increasing D on stomatal conductance.We manipulated cuticular conductance (gc) by three independent methods. First, we increased gc by using a solvent mixture applied to both leaf surfaces prior to determining stomatal responses to D; second, we increased gc by increasing leaf temperature at constant D; and third, we coated a small area of leaf with a light oil to decrease gc. In all three experiments, experimental data and model outputs showed very close agreement.We conclude, from the close agreement between model and experimental data and the fact that manipulations of gc, and hence cuticular transpiration, influenced gs in ways consistent with a feedback mechanism, that feedback is central in determining stomatal responses to D.