Impacts of water stress on gas exchange,water relations,chlorophyll content and leaf structure in the two main Tunisian olive (Olea europaea L.) cultivars

Leaf structural adaptations for the reduction of water loss were examined in two olive (Olea europaea L.) cultivars (Chemlali and Chétoui) growing under water stress conditions. Leaf measurements included leaf tissue thickness, stomatal density, trichome density, specific leaf area, leaf density, water relations, and gas exchange. We found considerable genotypic differences between the two cultivars. Chemlali exhibited more tolerance to water stress, with a thicker palisade parenchyma, and a higher stomatal and trichome density. Chemlali leaves also revealed lower specific leaf area and had higher density of foliar tissue and lower reduction in net CO₂ assimilation rate. The mechanisms employed by these two cultivars to cope with water deficit are discussed at the morpho-structural level. The morphological and structural characteristics of the leaves are in accordance with physiological observations and contribute to the interpretation of why the olive cv. Chemlali is more drought-tolerant than cv. Chetoui. Furthermore, from the behaviour of Chemlali plants we consider this cultivar very promising for cultivation in semi-arid areas.     

Variation in stomatal behaviour and gas exchange between mid-morning and mid-afternoon of north–south oriented grapevines (Vitis vinifera L. cv. Tempranillo) at different levels of soil water availability

A 3-year study was conducted to examine leaf gas exchange response of Vitis vinifera L. (cv. Tempranillo) grapevines growing in the central Iberian Peninsula as a function of soil water availability. Net CO₂ assimilation rate (A), stomatal conductance (g_s) and transpiration (E) of leaves were measured at the east and west side of vines planted in north/south orientated rows. Soil water availability was varied by three different irrigation treatments at 0.45, 0.30 and 0.15 of ETo and a fourth non-irrigated treatment. Approximately 60% of the variation in g_s over 3 years was due to changes in soil water content (θ_v); the correlation between the two was closer when examined on a season by season basis. Net CO₂ assimilation rates were significantly correlated with g_s. Stomatal conductance decreased by approximately 25–30% when measured 15:00 h (west side of vines) compared to 09:00 h (east side of vines); reductions in A were even greater than those in g_s. Leaf E increased approximately by 15–25% from morning to afternoon. The reduction in A and g_s from morning to afternoon was observed even in irrigated vines but absolute differences increased with decreasing soil water. This occurred when maximum daily g_s was less than 200 mmol m⁻² s⁻¹. These responses indicate that in hot areas training systems and row orientation, which minimize exposed leaf, area in the afternoon should be recommended.     

The effects of foliar applied CaCl2·2H2O,Ca(OH)2 and K2CO3 combined with the surfactants Glucopon and Plantacare on gas exchange of 1 year old apple (Malus domestica BORKH.) and broad bean (Vicia faba L.) leaves

Calcium chloride, calcium hydroxide, potassium carbonate and the alkylpolyglycoside surfactants Glucopon 215 CSUP and Plantacare 12 UP are salts applied to leaves as foliar nutrients and fungicides. These chemicals were sprayed on apple (Malus domestica BORKH.) and broad bean (Vicia faba L.) leaves. Stomatal conductance and rates of net photosynthesis were measured continuously in the light and in the dark using a Portable Photosynthesis System CIRAS-1. All compounds with the exception of Ca(OH)₂ affected stomatal conductance and net photosynthesis, albeit to different degrees. In light, Plantacare either alone (0.2 g l⁻¹) or in combination with CaCl₂·2H₂O (5 g l⁻¹) or K₂CO₃ (5 g l⁻¹) caused a rapid initial increase in stomatal conductance during the first 1–3 h after spraying on the leaves, maximum conductances were observed about 6 h after application. A rather high stomatal conductance was observed during the dark period when Glucopon (0.2 g l⁻¹) was applied either alone or in combination with Ca(OH)₂. The combination CaCl₂·2H₂O + Glucopon did not cause this elevated stomatal conductance during the dark. CaCl₂·2H₂O reduced stomatal conductance in combination with both Glucopon and Plantacare. The surfactant Plantacare reduced net photosynthesis during the first light period (12 h), if applied alone or in combination with CaCl₂·2H₂O. Treatment of broad bean leaves with K₂CO₃ + Plantacare resulted in a rapid decrease in net photosynthesis during the first hour, and then the rates of net photosynthesis increased rapidly and approached to those of the water control. The effects of surfactants and salts on net photosynthesis had nearly disappeared by the beginning of the second light period. Non-specific glycosidases presumably cleaved the glycosidic bond between the alkyl and the sugar moieties during the preceding night. Our data showed that foliar applications of CaCl₂·2H₂O and K₂CO₃ together with alkyl polyglycoside surfactants can affect gas exchange. However, the effects of the chemicals at the concentrations used in our study were not very large and were transient. They practically vanished within 24 h and a detrimental effect on growth and development of crops was not likely.