Within the growth zone, salt-affected leaves of sorghum (Sorghum bicolor) had narrower protoxylem and metaxylem cells than controls. Leaf width and cross-sectional area were also reduced, so that the salt treatment had no effect on the area of protoxylem per area of leaf cross section. Dye uptake studies suggested that in controls most of the veins, but in salt-affected leaves only half of the veins, are functional in water transport. Volumetric water flow was greatly diminished in the salt-affected plants. The reduced flow rate was largely explained by the salt-induced decrease in leaf surface area. Some decreases in flow rates per unit leaf mass or area were also produced by salinity, particularly in late developmental stages. Not surprisingly, leaf conductance measured with a diffusion porometer did not appear to be correlated with the diameter of the protoxylem or metaxylem elements. By contrast, published values of water deposition rates are strongly related to the size of the protoxylem elements: the rates of water deposition into the growing leaf tissue are proportional to the square of the protoxylem radius. Thus environmentally produced change of the hydraulic architecture of monocot leaves may cause change in local growth rates.

The hydraulic architecture of the secondary hemiepiphyte Monstera acuminata was examined in native plants from Los Tuxtlas, Veracruz, Mexico, to determine how it compared to better-known growth forms such as trees, shrubs, lianas and primary hemiepiphytes. Monstera acuminata starts its life cycle as a prostrate herb. As it ascends a tree or other vertical support, the stem becomes thicker, produces larger leaves, and may die back from the base upwards until only aerial feeding roots serve to connect the stem to the soil. Unlike the pattern of vessel-size distribution along the stems of woody dicotyledons, M. acuminata has its wider vessels at the top of the stem, decreasing in diameter towards the base. Also peculiar is the fact that Huber values (axis area/distal leaf area) tend to increase exponentially at higher positions within the plant. Based on the hydraulic conductivity (kh) and leaf-specific conductivity (LSC, kh/distal leaf area), the base of the stem potentially acts as a severe hydraulic constriction. This constriction is apparently not limiting, as aerial roots are produced further up the stem. The plants have remarkably strong root pressures, up to 225 kPa, which may contribute to the maintenance of functional vessels by refilling them at night or during periods of very high atmospheric humidity, as in foggy weather and rain. In common with dicotyledonous plants, vessel length, vessel diameter, kh, specific conductivity (ks, kh/axis area) and LSCs were all positively correlated with axis diameter. The features of the hydraulic architecture of M. acuminata may be an evolutionary consequence of an anatomical constraint (lack of vascular cambium and therefore of secondary growth) and the special requirements of the hemiepiphytic growth form.

Five evergreen subtropical tree species growing under identical environmental conditions were investigated to establish which hydraulic properties are genotypically rigid and which show phenotypic plasticity. Maximum xylem-specific conductivity (ks) correlated well with the anatomical characteristics (conduit diameter and density) for the four angiosperms Tecomaria capensis, Trichilia dregeana, Cinnamomum camphora and Barringtonia racemosa; the anatomy of the gymnosperm Podocarpus latifolius was not assessed. Huber values (functional xylem cross-sectional area [ratio ] leaf area) varied inversely with ks among species. Maximum leaf-specific conductivity was similar in the five unrelated species. Vulnerability of xylem to cavitation differed between species, as did the relationship between transpiration and water potential. Models of these parameters and isolated midday readings confirm that these trees operate at similar maximum leaf-specific conductivity (kl) values. The data are consistent with the hypothesis that conductivity characteristics (kl, ks) are influenced by environment, whereas vulnerability to cavitation is genetically determined.

Water relations, xylem embolism, root and shoot hydraulic conductance of both young plants in the field and potted seedlings of Quercus pubescens have been studied with the aim of investigating whether these variables may account for the well known adaptation of this oak species to arid habitats. Our data revealed that Q. pubescens is able to maintain high leaf relative water contents under water stress conditions. In fact, relative water contents measured in summer (July) did not differ from those recorded in April. This was apparently achieved by compensating water loss by an equal amount of water uptake. Such a drought avoidance strategy was made possible by the recorded high hydraulic efficiency of stems and roots under water stress. In fact, root hydraulic conductance of field-grown plants was maintained high in summer when the percentage loss of hydraulic conductance of stems was lowest. The hydraulic architecture of young plants of Q. pubescens measured in terms of partitioning of hydraulic resistances along the water pathway revealed that the highest hydraulic resistance was located in stems of the current year's growth. This hydraulic architecture is interpreted as consistent with the adaptation of Q. pubescens to arid habitats as a consequence of the recorded seasonal changes in water relation parameters as well as in root and stem hydraulics.