Water deficit negatively affects crop development and productivity. With decreasing rainfall and shortage of arable land, there is a demand for alternative drought-tolerant species for use on non-arable land. The tree species Balanites aegyptiaca is considered as drought tolerant and a potential source of many secondary metabolites. The oil-containing seeds may also be used as biofuel. Genetic diversity was investigated amongst the B. aegyptiaca collected from different geographical regions using amplified fragment length polymorphism (AFLP) and the relationship among geographical distribution and genetic diversity was determined. Plants were grown from seedlings collected at 12 locations from 11 provenances. AFLP produced 510 bands of which 477 (93.5%) were polymorphic. Cluster and principal component analyses indicated that individual samples of B. aegyptiaca were distributed in 3 main clades and that the provenance El-Kharga represented a single clade. Several key morphophysiological responses to water stress were examined to evaluate drought stress tolerance and to compare respective stress responses among different provenances under greenhouse conditions. Severe drought stress decreased biomass parameters in all genotypes. However, B. aegyptiaca provenances also differed in their adaptive responses to water shortage. By appropriate grouping of 2 or 3 response factors, the effects of water deficit on the various provenances could readily be distinguished. Provenance El-Kharga showed the smallest amount of biomass reduction under severe drought stress and retained the highest leaf water content.Key words: Amplified fragment length polymorphism (AFLP), Balanites aegyptiaca, biometrical growth parameters, drought tolerance, stomatal conductance.
INTRODUCTIONWater shortage is one of the major environmental limitations to plant growth and development (Harb et al., 2010;Song et al., 2012). Drought decreases crop productivity and approaching 28% of the world's soil surface is too dry to be reliably productive (Bray et al., 2002;Ambrosone et al., 2013). Plants respond to water shortage through several regulatory pathways and adapt by reprogramming a number of metabolic and physiological mechanisms (Morison et al., 2008;Ahuja et al., 2010;Park et al., 2012;Khamis and Papenbrock, 2014). Loss of water content closes stomata resulting in slower transpiration, photosynthesis, growth and gain in biomass. Stomatal pore size controlled through guard cells is the main control point affecting water use efficiency and the intake of CO 2 for photosynthesis (Song et al., 2014). Plants may respond to variation in soil water content through root signal(s) that originated from the root tips transferred via the xylem to the leaf (Cornic and Massacci, 1996) resulting in increasing the concentration of abscisic acid (ABA) up to 30-fold in the guard cell apoplast (William and Outlaw, 2003). This enhances ion outflow and leads to a reduction of solute concentration and a loss of turgor of the guard cells, finally resulting in stomatal ...