Hydraulic Failure Defines the Recovery and Point of Death in Water-Stressed Conifers

This study combines existing hydraulic principles with recently developed methods for probing leaf hydraulic function to determine whether xylem physiology can explain the dynamic response of gas exchange both during drought and in the recovery phase after rewatering. Four conifer species from wet and dry forests were exposed to a range of water stresses by withholding water and then rewatering to observe the recovery process. During both phases midday transpiration and leaf water potential (Ψ_leaf) were monitored. Stomatal responses to Ψ_leaf were established for each species and these relationships used to evaluate whether the recovery of gas exchange after drought was limited by postembolism hydraulic repair in leaves. Furthermore, the timing of gas-exchange recovery was used to determine the maximum survivable water stress for each species and this index compared with data for both leaf and stem vulnerability to water-stress-induced dysfunction measured for each species. Recovery of gas exchange after water stress took between 1 and >100 d and during this period all species showed strong 1:1 conformity to a combined hydraulic-stomatal limitation model (r² = 0.70 across all plants). Gas-exchange recovery time showed two distinct phases, a rapid overnight recovery in plants stressed to <50% loss of leaf hydraulic conductance (K_leaf) and a highly Ψ_leaf-dependent phase in plants stressed to >50% loss of K_leaf. Maximum recoverable water stress (Ψ_min) corresponded to a 95% loss of K_leaf. Thus, we conclude that xylem hydraulics represents a direct limit to the drought tolerance of these conifer species.     

Effect of Errors in Measuring Leaf Temperature and Ambient Gas Concentration on Calculated Resistances to CO(2) and Water Vapor Exchanges in Plant Leaves

Errors as small as 1 C in the measurement of leaf temperature (T_leaf) are shown to cause significant changes in the estimated value of the stomatal resistance (expressed in terms of total resistance to water vapor transfer, ∑rH₂O). The effect increases as T_leaf increases and as ambient relative humidity increases, if other conditions are maintained constant. The effect on the key CO₂ exchange parameter, the intracellular (or mesophyll) resistance, r_int, tends to be small under open stomata conditions but increases rapidly as stomatal closure occurs, particularly if the true value of r_int is relatively small.     

Utilization of leaf temperature for the selection of leaf gas-exchange traits to induce heat resistance in sunflower (Helianthus annuus L.)

Heat stress is a major production constraint of sunflower worldwide. Therefore, various populations (parental, F₁, F₂, F₃, and plant progenies) of sunflower were screened for leaf gas-exchange traits with the objectives to formulate selection criteria of heat resistance and development of heat-resistant lines. Initial screening and F₂ seeds exposed to heat stress (45°C) resulted in the development of an adapted F₂ population that showed leaf gas-exchange and morphological traits better than the unadapted population. Correlation coefficients of traits were partitioned into direct and indirect effects via a path analysis technique to determine the cause of their relationship with a basic parameter such as a reproductive head mass (HM). Path analysis showed a positive direct effect of leaf temperature (T_leaf) (0.32) on HM and also an indirect effect (0.77) of the transpiration rate (E) on HM. Moreover, T_leaf showed high heritability estimates. T_leaf was used to select superior plants within the F₂ population. This selection brought about an improvement in the net photosynthetic rate (P _N) and E as it was indicated from progeny performance and realized heritability. Progenies selected on the basis of T_leaf also showed an increase in achene yield and heat resistance over unselected F₃ progenies and a commercial hybrid.     

Measurement of Leaf Hydraulic Conductance and Stomatal Conductance and Their Responses to Irradiance and Dehydration Using the Evaporative Flux Method (EFM)

Water is a key resource, and the plant water transport system sets limits on maximum growth and drought tolerance. When plants open their stomata to achieve a high stomatal conductance (g_s) to capture CO₂ for photosynthesis, water is lost by transpiration^1,2. Water evaporating from the airspaces is replaced from cell walls, in turn drawing water from the xylem of leaf veins, in turn drawing from xylem in the stems and roots. As water is pulled through the system, it experiences hydraulic resistance, creating tension throughout the system and a low leaf water potential (Ψ_leaf). The leaf itself is a critical bottleneck in the whole plant system, accounting for on average 30% of the plant hydraulic resistance³. Leaf hydraulic conductance (K_leaf = 1/ leaf hydraulic resistance) is the ratio of the water flow rate to the water potential gradient across the leaf, and summarizes the behavior of a complex system: water moves through the petiole and through several orders of veins, exits into the bundle sheath and passes through or around mesophyll cells before evaporating into the airspace and being transpired from the stomata. K_leaf is of strong interest as an important physiological trait to compare species, quantifying the effectiveness of the leaf structure and physiology for water transport, and a key variable to investigate for its relationship to variation in structure (e.g., in leaf venation architecture) and its impacts on photosynthetic gas exchange. Further, K_leaf responds strongly to the internal and external leaf environment³. K_leaf can increase dramatically with irradiance apparently due to changes in the expression and activation of aquaporins, the proteins involved in water transport through membranes⁴, and K_leaf declines strongly during drought, due to cavitation and/or collapse of xylem conduits, and/or loss of permeability in the extra-xylem tissues due to mesophyll and bundle sheath cell shrinkage or aquaporin deactivation^5-10. Because K_leaf can constrain g_s and photosynthetic rate across species in well watered conditions and during drought, and thus limit whole-plant performance they may possibly determine species distributions especially as droughts increase in frequency and severity^11-14.We present a simple method for simultaneous determination of K_leaf and g_s on excised leaves. A transpiring leaf is connected by its petiole to tubing running to a water source on a balance. The loss of water from the balance is recorded to calculate the flow rate through the leaf. When steady state transpiration (E, mmol • m^-2 • s^-1) is reached, g_s is determined by dividing by vapor pressure deficit, and K_leaf by dividing by the water potential driving force determined using a pressure chamber (K_leaf= E /- Δψ_leaf, MPa)¹⁵.This method can be used to assess K_leaf responses to different irradiances and the vulnerability of K_leaf to dehydration^14,16,17.     

Leaf hydraulic safety margin and safety–efficiency trade-off across angiosperm woody species

Leaf hydraulic conductance and the vulnerability to water deficits have profound effects on plant distribution and mortality. In this study, we compiled a leaf hydraulic trait dataset with 311 species-at-site combinations from biomes worldwide. These traits included maximum leaf hydraulic conductance (K_leaf), water potential at 50% loss of K_leaf (P50_leaf), and minimum leaf water potential (Ψ_min). Leaf hydraulic safety margin (HSM_leaf) was calculated as the difference between Ψ_min and P50_leaf. Our results indicated that 70% of the studied species had a narrow HSM_leaf (less than 1 MPa), which was consistent with the global pattern of stem hydraulic safety margin. There was a positive relationship between HSM_leaf and aridity index (the ratio of mean annual precipitation to potential evapotranspiration), as species from humid sites tended to have larger HSM_leaf. We found a significant relationship between K_leaf and P50_leaf across global angiosperm woody species and within each of the different plant groups. This global analysis of leaf hydraulic traits improves our understanding of plant hydraulic response to environmental change.     

Co-ordination between leaf biomechanical resistance and hydraulic safety across 30 sub-tropical woody species

Background and AimsLeaf biomechanical resistance protects leaves from biotic and abiotic damage. Previous studies have revealed that enhancing leaf biomechanical resistance is costly for plant species and leads to an increase in leaf drought tolerance. We thus predicted that there is a functional correlation between leaf hydraulic safety and biomechanical characteristics.MethodsWe measured leaf morphological and anatomical traits, pressure–volume parameters, maximum leaf hydraulic conductance (K_leaf-max), leaf water potential at 50 % loss of hydraulic conductance (P50_leaf), leaf hydraulic safety margin (SM_leaf), and leaf force to tear (F_t) and punch (F_p) of 30 co-occurring woody species in a sub-tropical evergreen broadleaved forest. Linear regression analysis was performed to examine the relationships between biomechanical resistance and other leaf hydraulic traits.Key ResultsWe found that higher F_t and F_p values were significantly associated with a lower (more negative) P50_leaf and a larger SM_leaf, thereby confirming the correlation between leaf biomechanical resistance and hydraulic safety. However, leaf biomechanical resistance showed no correlation with K_leaf-max, although it was significantly and negatively correlated with leaf outside-xylem hydraulic conductance. In addition, we also found that there was a significant correlation between biomechanical resistance and the modulus of elasticity by excluding an outlier.ConclusionsThe findings of this study reveal leaf biomechanical–hydraulic safety correlation in sub-tropical woody species.     

Direct measurement of turgor and osmotic potential in individual epidermal cells : independent confirmation of leaf water potential as determined by in situ psychrometry

The pressure probe, which is routinely used to measure the turgor potential (Ψ_p) of individual epidermal cells in Tradescantia virginiana (L.), has also been used to sample small volumes of vacuolar fluid from these same cells (as low as 0.02 nl) for measurement of cellular solute (osmotic) potential (Ψ_s) in a micro freezing point osmometer. The water potential components Ψ_p and Ψ_o have been used to calculate the total water potential of individual epidermal cells (Ψ_cell) which has then been directly compared to the total leaf water potential (Ψ_leaf) measured psychrometrically. The relation of Ψ_leaf and Ψ_cell to leaf transpiration indicates that in T. virginiana, a relatively straightforward relation exists between the level of water flow through the leaf tissue, and the ΔΨ within the leaf, between two points along the water flow pathway. Substantial agreement was found between the two independent, in situ methods of measuring Ψ when extrapolated to zero transpiration conditions. These results are discussed with respect to the thermodynamics of water transport in plant tissues.     

Within-branch heterogeneity of the light environment and leaf temperature in a Fagus crenata crown and its significance for photosynthesis calculations

On days with clear skies in late August 2002 diurnal changes in the within-branch heterogeneity of photosynthetic photon flux density at the leaf surface (PPFD_s) and leaf temperature (T _leaf) were measured at natural leaf orientations in the upper and lower layers of a Fagus crenata crown. The PPFD_s and T _leaf measurements were converted to branch photosynthesis rates (P _B; μmol s⁻¹) using a photosynthetic model proposed by Farquhar et al. (Planta 149:78–90, 1980), an empirical stomatal conductance model suggested by Leuning et al. (Plant Cell Environ 18:339–335, 1995), and the total leaf area of the branches. To evaluate the importance of the variation in PPFD_s and T _leaf on photosynthesis calculations, P _B calculated with the observed variation in PPFD_s and T _leaf was compared with estimates, based on the average (variation-free) values of PPFD_s and T _leaf, respectively. In both the layers, daily total P _B values obtained with T _leaf averaging were very close to those obtained with no averaging because of the weak inflection of the net photosynthesis rate (P _n) to T _leaf curves in the observed T _leaf ranges (24.4–36.5 and 21.9–29.1°C in the upper and lower layers, respectively) and relatively small variation in within-branch T _leaf at each time of day. This finding applied across potential climate conditions on fine days in August (T _leaf range of 19.4–41.5 and 16.9–34.1°C in the upper and lower layers, respectively) and when the spatial scale was increased from branch to leaf layer, which increased the maximum variation in within-branch T _leaf from 7.8 to 9.5°C and 4.5 to 5.5°C in the upper and lower layers, respectively. In contrast, averaging PPFD_s caused 25–50% and 41–90% overestimation of daily total P _B in the upper and lower layers, respectively, due to the sharp curvature in the PPFD_s response curve to P _n, and relatively large variation in within-branch PPFD_s. Further, it led to overestimation of midday depression of P _B in the upper layer, possibly because branch structural acclimation to incident light was neglected. Our results indicate that averaged values of T _leaf could be used for the estimation of carbon gain at layer scale throughout August, but spatial variations in PPFD_s need to be considered in detail for reliable estimates of carbon gain.     

Acclimation of Foliar Respiration and Photosynthesis in Response to Experimental Warming in a Temperate Steppe in Northern China

Background

Thermal acclimation of foliar respiration and photosynthesis is critical for projection of changes in carbon exchange of terrestrial ecosystems under global warming.

Methodology/Principal Findings

A field manipulative experiment was conducted to elevate foliar temperature (T _leaf) by 2.07°C in a temperate steppe in northern China. R _d/T _leaf curves (responses of dark respiration to T _leaf), A _n/T _leaf curves (responses of light-saturated net CO₂ assimilation rates to T _leaf), responses of biochemical limitations and diffusion limitations in gross CO₂ assimilation rates (A _g) to T _leaf, and foliar nitrogen (N) concentration in Stipa krylovii Roshev. were measured in 2010 (a dry year) and 2011 (a wet year). Significant thermal acclimation of R _d to 6-year experimental warming was found. However, A _n had a limited ability to acclimate to a warmer climate regime. Thermal acclimation of R _d was associated with not only the direct effects of warming, but also the changes in foliar N concentration induced by warming.

Conclusions/Significance

Warming decreased the temperature sensitivity (Q ₁₀) of the response of R _d/A _g ratio to T _leaf. Our findings may have important implications for improving ecosystem models in simulating carbon cycles and advancing understanding on the interactions between climate change and ecosystem functions.     

Temperature responses of photosynthesis and leaf hydraulic conductance in rice and wheat

Studies on the temperature (T) responses of photosynthesis and leaf hydraulic conductance (K_leaf) are important to plant gas exchange. In this study, the temperature responses of photosynthesis and K_leaf were studied in Shanyou 63 (Oryza sativa) and Yannong 19 (Triticum aestivum). Leaf water potential (Ψ_leaf) was insensitive to T in Shanyou 63, while it significantly decreased with T in Yannong 19. The differential Ψ_leaf − T relationship partially accounted for the differing g_m–T relationships, where g_m was less sensitive to T in Yannong 19 than in Shanyou 63. With different g_m–T and Ψ_leaf–T relationships, the temperature responses of photosynthetic limitations were surprisingly similar between the two lines, and the photosynthetic rate was highly correlated with g_m. With the increasing T, K_leaf increased in Shanyou 63 while it decreased in Yannong 19. The different K_leaf–T relationships were related to different Ψ_leaf–T relationships. When excluding the effects of water viscosity and Ψ_leaf, K_leaf was insensitive to T in both lines. g_m and K_leaf were generally not coordinated across different temperatures. This study highlights the importance of Ψ_leaf on leaf carbon and water exchanges, and the mechanisms for the g_m–T and K_leaf–T relationships were discussed.     

Water potential in excised leaf tissue: comparison of a commercial dew point hygrometer and a thermocouple psychrometer on soybean, wheat, and barley

Leaf water potential (Ψ_leaf) determinations were made on excised leaf samples using a commercial dew point hygrometer (Wescor Inc., Logan, Utah) and a thermocouple psychrometer operated in the isopiestic mode. With soybean leaves (Glycine max L.), there was good agreement between instruments; equilibration times were 2 to 3 hours. With cereals (Triticum aestivum L. and Hordeum vulgare L.), agreement between instruments was poor for moderately wilted leaves when 7-mm-diameter punches were used in the hygrometer and 20-mm slices were used in the psychrometer, because the Ψ_leaf values from the dew point hygrometer were too high. Agreement was improved by replacing the 7-mm punch samples in the hygrometer by 13-mm slices, which had a lower cut edge to volume ratio. Equilibration times for cereals were normally 6 to 8 hours. Spuriously high Ψ_leaf values obtained with 7-mm leaf punches may be associated with the ion release and reabsorption that occur upon tissue excision; such errors evidently depend both on the species and on tissue water status.     

POST-BURN DIFFERENCES IN SOLAR RADIATION,LEAF TEMPERATURE AND WATER STRESS INFLUENCING PRODUCTION IN A LOWLAND TALLGRASS PRAIRIE

The influence of standing dead biomass on available solar radiation, leaf temperature (T_leaf) and leaf water potential (ѱ_leaf) of Andropogon gerardii in unburned tallgrass prairie was compared to burned prairie in eastern Kansas. The standing dead reduced photosynthetically active radiation incident on emerging shoots by 58.8% in unburned compared to burned prairie during the initial 30 days of the growing season. Aboveground production in unburned prairie was similarly reduced during this period (55.4%) compared to burned prairie. Leaf temperatures in A. gerardii were greater in unburned prairie than in burned early in the season, but were nearly equal by the end of the growing season. The maximum elevation of T_leaf in unburned prairie above burned was 9.5 C. The maximum unburned T_leaf measured was 41.5 C compared to 39.4 C in burned prairie. Lower windspeed adjacent to leaves in unburned prairie resulting in reduced convective cooling may have caused higher T_leaf in unburned prairie. Leaf water potential was significantly lower in unburned prairie than in burned prairie early in the season but was higher in unburned prairie by late season. The seasonal minimum ѱ_leaf in burned prairie was — 1.60 MPa compared to —1.45 MPa in unburned prairie. The combined effect of these post-burn differences in solar radiation, T_leaf and ѱ_leaf may be significant in contributing to the lower production in unburned compared to burned tallgrass prairie.     

Neither xylem collapse,cavitation, or changing leaf conductance drive stomatal closure in wheat

Identifying the drivers of stomatal closure and leaf damage during stress in grasses is a critical prerequisite for understanding crop resilience. Here, we investigated whether changes in stomatal conductance (g_s) during dehydration were associated with changes in leaf hydraulic conductance (K_leaf), xylem cavitation, xylem collapse, and leaf cell turgor in wheat (Triticum aestivum). During soil dehydration, the decline of g_s was concomitant with declining K_leaf under mild water stress. This early decline of leaf hydraulic conductance was not driven by cavitation, as the first cavitation events in leaf and stem were detected well after K_leaf had declined. Xylem vessel deformation could only account for <5% of the observed decline in leaf hydraulic conductance during dehydration. Thus, we concluded that changes in the hydraulic conductance of tissues outside the xylem were responsible for the majority of K_leaf decline during leaf dehydration in wheat. However, the contribution of leaf resistance to whole plant resistance was less than other tissues (<35% of whole plant resistance), and this proportion remained constant as plants dehydrated, indicating that K_leaf decline during water stress was not a major driver of stomatal closure.     

Leaf physiology does not predict leaf habit; examples from tropical dry forest

Leaf structure and physiology are thought to be closely linked to leaf longevity and leaf habit. Here we compare the seasonal variation in leaf hydraulic conductance (k_leaf) and water potential of two evergreen tree species with contrasting leaf life spans, and two species with similar leaf longevity but contrasting leaf habit, one being deciduous and the other evergreen. One of the evergreen species, Simarouba glauca, produced relatively short-lived leaves that maintained high hydraulic conductance year round by periodic flushing. The other evergreen species, Quercus oleoides, produced longer-lived leaves with lower k_leaf and as a result minimum leaf water potential was much lower than in S. glauca (–2.8 MPa vs –1.6 MPa). Associated with exposure to lower water potentials, Q. oleoides leaves were harder, had a higher modulus of elasticity, and were less vulnerable to cavitation than S. glauca leaves. Both species operate at water potentials capable of inducing 20 (S. glauca) to 50% (Q. oleoides) loss of k_leaf during the dry season although no evidence of cumulative losses in k_leaf were observed in either species suggesting regular repair of embolisms. Leaf longevity in the deciduous species Rhedera trinervis is similar to that of S. glauca, although maximum k_leaf was lower. Furthermore, a decline in leaf water potential at the onset of the dry season led to cumulative losses in k_leaf in R. trinervis that culminated in leaf shedding.     

Effect of dietary supplementation of Neem,Azadirachta indica leaf extracts on enhancing the growth performance,chemical composition and survival of rainbow trout,Oncorhynchus mykiss

Rainbow trout Oncorhynchus mykiss has a great nutritional value and delicious taste. A 90-days experimental trial was conducted to investigate the effect of dietary leaf extract of neem tree Azadirachta indica as a feeding supplement on the growth performance and proximate composition of O. mykiss. Four experimental diets were designed as T₁ (with 5% A. indica leaf extract), T₂ (with 7% of A. indica leaf extract), T₃ (with 10% A. indica leaf extract), and T₄ (control group feed with a regular diet with 0% A. indica leaf extract). The average initial weight of fry 0.4 ± 0.14 g was stocked at 25 fish/tank with two replicates per treatment (4 × 2 = 8). After 90 days of the experimental trial, One-way ANOVA showed significant differences in final body weight, weight gain, specific growth rate, feed conversion ratio, and survival rate among the treatment groups (p < 0.05). The highest final body weight (48.10 g) and weight gain (47.70 g) was observed in T2 with 7% A. indica leaf extract, which was significantly different from the other treatments (p < 0.05). The lowest FCR was recorded in T2 (1.90), which was significantly different compared to other treatment groups (p < 0.05). Inclusion of A. indica leaf extract in formulated feed for rainbow trout had significant effects in the hepatosomatic index, viscerosomatic index and Fulton’s condition factor (p < 0.05), but there was no significant difference in the survival rate of rainbow trout fry treated with different experimental diets (p > 0.05). The phenomenal regression indicates that 7.5% A. indica inclusion is optimum for best growth performance for rainbow trout under a controlled environment. Thus, the present study suggests that the dietary leaf extract has performed an excellent nutritional supplement by enhancing growth performance and health conditions of rainbow trout in the hatchery conditions.     

Estimation of whole-plant resistance to gaseous exchange independent of leaf temperature measurement

For studies into the uptake of mercury vapor by wheat (Triticum aestivum), a simple theory and plant chamber were employed to estimate total leaf resistance of whole plants to water vapor exchange. The estimates were independent of leaf temperature, for which mean values were indirectly determined. The approach involved the measurement, at steady-state conditions, of the net change in water vapor flux per unit of leaf surface (Δq_v) in response to a small induced change in absolute humidity (ΔC_a). Assuming that total leaf resistance (r_l) was constant and that change in leaf temperature (T_l) was negligible, total leaf resistance was calculated from the equation, [Formula: see text]     

Assessing the role of vertical leaves within the photosynthetic function of Styrax camporum under drought conditions

Previous evidence has demonstrated that vertical leaves of Styrax camporum, a woody shrub from the Brazilian savanna, have a higher net photosynthetic rate (P _N) compared with horizontal leaves, and that it is detected only if gas exchange is measured with light interception by both leaf surfaces. In the present study, leaf temperature (T _leaf), gas exchange and chlorophyll (Chl) a fluorescence with light interception on adaxial and also on abaxial surfaces of vertical and horizontal mature fully-expanded leaves subjected to water deficit (WD) were measured. Similar gas-exchange and fluorescence values were found when the leaves were measured with light interception on the respective surfaces of horizontal and vertical leaves. WD reduced P _N values measured with light interception on leaf surfaces of both leaf types, but the effective quantum yield of PSII (Φ_PSII) and the apparent electron transport rate (ETR) were reduced only when the leaves were measured with light interception on the adaxial surface. WD did not decrease the maximum quantum yield of PSII (F_v/F_m) or increase T _leaf, even at the peak of WD stress. Vertical leaf orientation in S. camporum is not related to leaf heat avoidance. In addition, the similar P _N values and the lack of higher values of Φ_PSII and ETR in vertical compared with horizontal leaves measured with light interception by each of the leaf surfaces suggests that the vertical leaf position is not related to photoprotection in this species, even when subjected to drought conditions. The exclusion of this photoprotective role could raise the alternative hypothesis that diverse leaf angles sustain whole plant light interception efficiency increased in this species.     

Estimating Finite Rate of Population Increase for Sharks Based on Vital Parameters

The vital parameter data for 62 stocks, covering 38 species, collected from the literature, including parameters of age, growth, and reproduction, were log-transformed and analyzed using multivariate analyses. Three groups were identified and empirical equations were developed for each to describe the relationships between the predicted finite rates of population increase (λ’) and the vital parameters, maximum age (T_max), age at maturity (T_m), annual fecundity (f/R_c)), size at birth (L_b), size at maturity (L_m), and asymptotic length (L_∞). Group (1) included species with slow growth rates (0.034 yr^-1 < k < 0.103 yr^-1) and extended longevity (26 yr < T_max < 81 yr), e.g., shortfin mako Isurus oxyrinchus, dusky shark Carcharhinus obscurus, etc.; Group (2) included species with fast growth rates (0.103 yr^-1 < k < 0.358 yr^-1) and short longevity (9 yr < T_max < 26 yr), e.g., starspotted smoothhound Mustelus manazo, gray smoothhound M. californicus, etc.; Group (3) included late maturing species (L_m/L_∞ ≧ 0.75) with moderate longevity (T_max < 29 yr), e.g., pelagic thresher Alopias pelagicus, sevengill shark Notorynchus cepedianus. The empirical equation for all data pooled was also developed. The λ’ values estimated by these empirical equations showed good agreement with those calculated using conventional demographic analysis. The predictability was further validated by an independent data set of three species. The empirical equations developed in this study not only reduce the uncertainties in estimation but also account for the difference in life history among groups. This method therefore provides an efficient and effective approach to the implementation of precautionary shark management measures.     

Changes in leaf hydraulic conductance correlate with leaf vein embolism in<Emphasis Type="Italic"> Cercis siliquastrum</Emphasis> L.

The impact of xylem cavitation and embolism on leaf (K _leaf) and stem (K _stem) hydraulic conductance was measured in current-year shoots of Cercis siliquastrum L. (Judas tree) using the vacuum chamber technique. K _stem decreased at leaf water potentials (Ψ_L) lower than ?1.0 MPa, while K _leaf started to decrease only at Ψ_L L K _leaf changes. Field measurements of leaf conductance to water vapour (g _L) and Ψ_L showed that stomata closed when Ψ_L decreased below the Ψ_L threshold inducing loss of hydraulic conductance in the leaf. The partitioning of hydraulic resistances within shoots and leaves was measured using the high-pressure flow meter method. The ratio of leaf to shoot hydraulic resistance was about 0.8, suggesting that stem cavitation had a limited impact on whole shoot hydraulic conductance. We suggest that stomatal aperture may be regulated by the cavitation-induced reduction of hydraulic conductance of the soil-to-leaf water pathway which, in turn, strongly depends on the hydraulic architecture of the plant and, in particular, on leaf hydraulics.     

Circadian regulation of leaf hydraulic conductance in sunflower (Helianthus annuus L. cv Margot)

The circadian regulation of leaf hydraulic conductance (K_leaf) was investigated in Helianthus annuus L. (sunflower). K_leaf was measured with an high pressure flow meter during the light and dark period from plants growing at a photoperiod of 12 h. K_leaf was 4.0 e−4 kg s⁻¹ m⁻² MPa⁻¹ during the light period (LL) and 30–40% less during the dark period (DL). When photoperiod was inverted and leaves were measured for K_leaf at their subjective light or dark periods, K_leaf adjusted to the new conditions requiring 48 h for increasing from dark to light values and 4 d for the opposite transition. Plants put in continuous dark showed K_leaf oscillating from light to dark values in phase with their subjective photoperiod indicating that K_leaf changes were induced by the circadian clock. Several cuts through the minor veins reduced leaf hydraulic resistance (R_leaf) of both LL and DL to the same value (1.0 e + 3 MPa m² s kg⁻¹) that equalled the vascular resistance (R_v). The contribution of the non-vascular leaf resistance (R_nv) to R_leaf was of 71.9% in DL and of 58.4% in LL. The dominant R_nv was shown to be reversibly modulated by mercurials, suggesting that aquaporins play a role in diurnal changes of K_leaf.