A new expression for ion leakage from plant tissue, the tissue ionic conductance (gT), is compared with electrical conductivity (EC) and a commonly used damage index (Id) to test the ability of each expression to correctly describe leakiness in two model systems representing examples of physiological processes with well-known effects on membrane permeability. In experiments in which drought-acclimated leaves were compared with nonacclimated leaves and senescing leaves were compared with nonsenescing leaves, Id contradicted our expectation that acclimated tissue would be less leaky than nonacclimated tissue, and gT1and EC confirmed this expectation. In a comparison of senescing and nonsenescing tissue, Id again contradicted our expectation that senescing tissue would be more leaky than nonsenescing, and EC and gT, were confirming. Using a diffusion analysis approach, we show that Id fails to account for variation in the concentration gradient between the tissue and the bathing solution and variation in the surface area through which efflux occurs. Furthermore, because Id is a parameter that relates treatment performance to control performance as a percentage value, it distorts the actual differences among treatments. The resulting artifacts lead to a presentation of membrane integrity which is probably incorrect.EC is a more direct measurement of net ion efflux and appears to be less vulnerable to artifact. However, because gTi is the only expression that explicitly includes chemical driving force and tissue surface area, it is the most reliable of the three expressions.Measuring solute leakage from plant tissue is a long-standing method for estimating membrane permeability in relation to environmental stresses, growth and development, and genotypic variation. Early published accounts used total electrolyte leakage, expressed as specific conductance (EC2) of the aqueous bathing solution in which the tissue was immersed, to indicate degree of damage resulting from chilling injury (3,4)

Tissue osmotic potential(Ψπ) and solute constituents were evaluated in leaves and roots of well-watered and water-stressed Prunus avium L. × pseudocerasus Lindl. `Colt' and Prunus cerasus L. `Meteor'. Osmotic potential at full turgorΨπ,sat decreased in response to water stress for leaves and roots of both cultivars. For `Colt', a cultivar with an indeterminate growth habit,Ψπ,sat decreased by 0.56 MPa and 0.38 MPa for terminal expanding leaves and older expanded leaves, respectively. For `Meteor', a cultivar with a determinate growth habit,Ψπ,sat decreased by ≈0.47 MPa in both terminal and older leaves. RootΨπ,sat was alike for both cultivars and showed a similar decrease of 0.20 MPa in response to water stress. Roots had considerably higherΨπ,sat than did leaves in both cultivars, irrespective of irrigation treatment. Soluble carbohydrates and potassium (K+) were the major solute constituents in both cultivars. Of the soluble carbohydrates, sorbitol was found in the greatest concentration and accounted for the bulk of water stress-induced solute accumulation in both cultivars. Regardless of the irrigation treatment, mature leaves of `Meteor' consistently had lowerΨπ,sat (typically 0.4 MPa) than `Colt'. This variation in Ψπ,sat between Prunus cultivars suggests the potential for selection of cultivars with low Ψπ,sat and possibly superior drought resistance.

In vitro regeneration systems provide a powerful tool for manipulating ploidy to facilitate breeding and development of new crops. Polyploid induction can expand breeding opportunities, assist with the development of seedless triploid cultivars, enhance ornamental characteristics and environmental tolerances, increase biomass and restore fertility in wide hybrids. In vitro ploidy manipulation is commonly induced using antimitotic agents such as colchicine, oryzalin and trifluralin, while many other antimitotic agents have been relatively unexplored. Successful induction requires a synergistic pairing of efficient penetration of the antimitotic agent and may be dependent the length of exposure and concentrations of antimitotic agents, tissue types, and interactions with basal media and plant growth regulators. In vitro conditions vary among taxa and individual genera, species, and cultivars, often requiring unique treatments to maximize polyploid induction. In some taxa, the induction of polyploidy influences in vitro growth, development, and root formation. Here we provide an overview of mitotic inhibitors and their application for in vitro ploidy manipulation for plant breeding and crop improvement.

No abstract

Net photosynthesis (Pn) of two ecotypes of redbud (Cercis canadensis L.) was studied following growth under high temperatures and increasing drought. Although mexican redbud [C. canadensis var. mexicana (Rose) M. Hopkins] exhibited greater Pn than eastern redbud (C. canadensis var. canadensis L.), Pn decreased at a similar rate under water deficit stress for both ecotypes. Mexican redbud also had greater instantaneous water use efficiency [net photosynthesis: transpiration (WUE)] than eastern redbud. Differences in both Pn and WUE might have been due to differences in leaf thickness. The optimum temperature for potential photosynthetic capacity (37 °C) was unaffected by irrigation or ecotype. Tissue osmotic potential at full turgor was more negative in eastern redbud, but was unaffected by drought stress in either ecotype. Soluble carbohydrate content was higher in eastern redbud, and in both ecotypes, d-pinitol was the major soluble carbohydrate and was considerably more abundant in the water-stressed plants. Total polyol content (myo-inositol + ononitol + pinitol) was also greater in the water-stressed plants. Both ecotypes were very tolerant of high temperatures and drought.