Reduced stomatal conductance (gs ) during soil drought in angiosperms may result from effects of leaf turgor on stomata and/or factors that do not directly depend on leaf turgor, including root-derived abscisic acid (ABA) signals. To quantify the roles of leaf turgor-mediated and leaf turgor-independent mechanisms in gs decline during drought, we measured drought responses of gs and water relations in three woody species (almond, grapevine and olive) under a range of conditions designed to generate independent variation in leaf and root turgor, including diurnal variation in evaporative demand and changes in plant hydraulic conductance and leaf osmotic pressure. We then applied these data to a process-based gs model and used a novel method to partition observed declines in gs during drought into contributions from each parameter in the model. Soil drought reduced gs by 63-84% across species, and the model reproduced these changes well (r(2)  = 0.91, P < 0.0001, n = 44) despite having only a single fitted parameter. Our analysis concluded that responses mediated by leaf turgor could explain over 87% of the observed decline in gs across species, adding to a growing body of evidence that challenges the root ABA-centric model of stomatal responses to drought.

Sarcocornia fruticosa (L.) A.J. Scott is found in coastal marshes of south-west Spain, growing under a very wide range of interstitial soil salinity from 10 mM up to nearly 1000 mM. A glasshouse experiment was designed to investigate the effect of this range of salinities on the morphology and the photosynthetic apparatus of S. fruticosa by measuring growth rate, photosynthetic and non-photosynthetic area, atrophy of distal branch ends, water status, chlorophyll fluorescence parameters, gas exchange and photosynthetic pigment concentrations. The long-term effects of salinity on the growth of S. fruticosa were mainly determined by the extent of photosynthetic area rather than the variations in net photosynthetic rate. Photosynthetic area was reduced at 1030 mM as a result of a decrease in the length of the photosynthetic portions. This was induced by fewer internodes and, at salinities lower than 510 mM, smaller internode diameter. Net photosynthetic rate increased as the quantum efficiency of photosystem II decreased in the different salinity treatments, which means that the plant could be increasing photorespiration and/or using cyclic electron transport as additional photoprotective mechanisms. The recorded drop in net photosynthetic rate at higher salinities appeared to be due to a reduction in stomatal conductance. The results indicate that S. fruticosa is capable of tolerating very high and continued exposure to salt, showing its greatest growth rate at 510 mM NaCl.

Abstract. Nitrate reductase (NR, NADH:nitrate oxidoreductase, EC 1.6.6.1) from barley (Hordeum vulgate L.cv. Hassan) leaves was inactivated during a light-dark transition, losing approx. 50% of activity after 30 min of darkness. The dark inactivation was reversed by illumination of the seedlings, the kinetics of reactivation being similar to those of inactivation. High extractable NR activity and significant differences between illuminated and darkened leaves were observed in media containing EDTA and inorganic phosphate (P~). Addition of Ca 2+ ions during extraction and assay decreased NR activity from illuminated and darkened leaves, enhancing the light-dark difference. While no clear correlation could be found between irradiance and NR activity, a hyperbolic correlation appeared between extractable NR activity and in-vivo rates of COs fixation, indicating that NR activation follows saturation kinetics with respect to CO2 fixation. Furthermore, hexoses and hexose-phosphates fed to the leaves via the transpiration stream protected against the dark-inactivation of NR. The results indicate that carbon-assimilation products are regulatory factors of NR activity in barley leaves, mediating both the lightdark modulation of NR and its dependence upon CO2 fixation.

Wild subspecies of Olea europaea constitute a source of genetic variability with huge potential for olive breeding to face global changes in Mediterranean-climate regions. We intend to identify wild olive genotypes with optimal adaptability to different environmental conditions to serve as a source of rootstocks and resistance genes for olive breeding. The SILVOLIVE collection includes 146 wild genotypes representative of the six O. europaea subspecies and early-generations hybrids. These genotypes came either from olive germplasm collections or from direct prospection in Spain, continental Africa and the Macaronesian archipelago. The collection was genotyped with plastid and nuclear markers, confirming the origin of the genotypes and their high genetic variability. Morphological and architectural parameters were quantified in 103 genotypes allowing the identification of three major groups of correlative traits including vigor, branching habits and the belowground-to-aboveground ratio. The occurrence of strong phenotypic variability in these traits within the germplasm collection has been shown. Furthermore, wild olive relatives are of great significance to be used as rootstocks for olive cultivation. Thus, as a proof of concept, different wild genotypes used as rootstocks were shown to regulate vigor parameters of the grafted cultivar "Picual" scion, which could improve the productivity of high-density hedgerow orchards.

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