Chlorophyll a fluorescence, water potential (Ψs), and root system of Juniperus oxycedrus ssp. macrocarpa, Juniperus phoenicea ssp. turbinata, and Pinus pinea were studied in Mediterranean coastal dunes of SW Spain during summer drought and after fall rains in 1999, the driest year in the 90's. A strong and reversible depression in the photochemical efficiency of photosystem 2 of the three species was recorded, which happened concomitantly with the diurnal increase and decrease in radiation. J. phoenicea, with superficial root system, was the most affected species by summer drought. It showed high rates of down-regulation of photosynthesis by photoinhibition and positive correlation between Ψs and Fv/Fp, with Ψs lower than -7 MPa. However, it tolerated this high stress, showing a fast recovery of its physiological state after fall rains. On the other hand, J. oxycedrus and P. pinea, both with deep root systems, kept their Ψs values up to -3 MPa, showing lower stress during summer drought. On the other hand, J. oxycedrus and J. phoenicea were more sensible to changes in edaphic water content than P. pinea. These specific responses to summer drought would be determined by their root distributions and stomatal control of transpiration, conditioning the efficiency in getting and using the available water resources. Ecophysiological responses indicate that these species are well-adapted to long periods of drought in Mediterranean climate areas, developing different strategies: J. phoenicea tolerates high stress with a fast recovery after fall rains, while J. oxycedrus and P. pinea are less affected by summer drought since their deep root systems would allow them to reach deep water resources. and J. M. Castillo ... [et al.].
Effects of benzyladenine (BA) and abscisic acid (ABA) applied separately or simultaneously on parameters of gas exchange of Phaseolus vulgaris L. leaves were studied. In the first two experimental sets) 100 μM ABA and 10 μM BA were applied to plants sufficiently supplied with water. Spraying of leaves with ABA decreased stomatal conductance (gs) and in consequence transpiration rate (E) and net photosynthetic rate (PN) already 1 h after application, but 24 h after application the effect almost disappeared. 10 μM BA slightly decreased gas exchange parameters, but in simultaneous application with ABA reversed the effect of ABA. Immersion of roots into the same solutions markedly decreased gas exchange parameters and 24 h after ABA application the stomata were completely closed. The effect of ABA was ameliorated by simultaneous BA application, particularly after 1-h treatment. In the third experimental set, plants were pre-treated by immersing roots into water, 1 μM BA, or 100 μM ABA for 24 h and then the halves of split root system were dipped into different combinations of 1 μM BA, 100 μM ABA, and water. In plants pre-treated with ABA all gas exchange parameters were small and they did not differ in plants treated with H2O+H2O, H2O+BA, or BA+BA. In plants pre-treated with BA or H2O, markedly lower values of PN were found when both halves of roots were immersed in ABA. Further, the effects of pre-treatment of plants with water, 1 μM BA, 100 μM ABA, or ABA+BA on the development of water stress induced by cessation of watering and on the recovery after rehydration were followed. ABA markedly decreased gas exchange parameters at the beginning of the experiment, but in its later phase the effect was compensated by delay in development of water stress. BA also delayed development of water stress and increased PN in water-stressed leaves. BA reversed the effect of ABA at mild water stress. Positive effects of BA and ABA pre-treatments were observed also after rehydration.