Phenotypic variation of root-system architecture under high P and low P conditions in potato (Solanum tuberosum L.).

BACKGROUND: Phosphorus (P) is an essential macronutrient required for plant metabolism and growth. Its acquisition by plants depends on the availability of dissolved P in the rhizosphere and on the characteristics of P uptake mechanisms such as root-system architecture (RSA). Compared to other crops, potato (Solanum tuberosum L.) has a relatively poor P acquisition efficiency. This is mainly due to its shallow and sparsely branched root system, resulting in a rather limited exploitable soil volume. Information about potato genotypes with RSA traits suitable to improve adaptation to nutrient scarcity is quite rare. Aim of this study is to assess phenotypic variation of RSA in a potato diversity set and its reactions to P deficiency. RESULTS: Only one out of 22 RSA-traits showed a significant increase under low-P conditions. This indicates an overall negative effect of P scarcity on potato root growth. Differences among genotypes, however, were statistically significant for 21 traits, revealing a high variability in potato RSA. Using a principal component analysis (PCA), we were able to classify genotypes into three groups with regard to their root-system size. Genotypes with both small and large root systems reacted to low-P conditions by in- or decreasing their relative root-system size to medium, whereas genotypes with an intermediate root system size showed little to no changes. CONCLUSIONS: We observed a huge variation in both the potato root system itself and its adaptation to P deficiency. This may enable the selection of potato genotypes with an improved root-zone exploitation. Eventually, these could be utilized to develop new cultivars adapted to low-P environments with better resource-use efficiencies.

Proton exchange membrane developed from novel blends of polybenzimidazole and poly(vinyl-1,2,4-triazole).

In continuation (J. Phys. Chem. B2008, 112, 5305; J. Colloid Interface Sci. 2010, 351, 374) of our quest for proton exchange membrane (PEM) developed from polybenzimidazole (PBI) blends, novel polymer blend membranes of PBI and poly(1-vinyl-1,2,4-triazole) (PVT) were prepared using a solution blending method. The aim of the work was to investigate the effect of the blend composition on the properties, e.g., thermo-mechanical stability, swelling, and proton conductivity of the blend membranes. The presence of specific interactions between the two polymers in the blends were observed by studying the samples using varieties of spectroscopic techniques. Blends prepared in all possible compositions were studied using a differential scanning calorimetry (DSC) and exhibited a single T(g) value, which lies between the T(g) value of the neat polymers. The presence of a single composition-dependent T(g) value indicated that the blend is a miscible blend. The N-H···N interactions between the two polymers were found to be the driving force for the miscibility. Thermal stability up to 300 °C of the blend membranes, obtained from thermogravimetric analysis, ensured their suitability as PEMs for high-temperature fuel cells. The proton conductivity of the blend membranes have improved significantly, compared to neat PBI, because of the presence of triazole moiety, which acts as a proton facilitator in the conduction process. The blend membranes showed a considerably lower increase in thickness and swelling ratio than that of PBI after doping with phosphoric acid (PA). We found that the porous morphology of the blend membranes caused the loading of a larger amount of PA and, consequently, higher proton conduction with lower activation energy, compared to neat PBI.

Formation of core (polystyrene)-shell (polybenzimidazole) nanoparticles using sulfonated polystyrene as template.

We report formation of core (polystyrene)-shell (polybenzimidazole) nanoparticles from a new blend system consisting of an amorphous polymer polybenzimidazole (PBI) and an ionomer sodium salt of sulfonated polystyrene (SPS-Na). The ionomer used for the blending is spherical in shape with sulfonate groups on the surface of the particles. An in depth investigation of the blends at various sulfonation degrees and compositions using Fourier transform infrared (FT-IR) spectroscopy provides direct evidence of specific hydrogen bonding interactions between the N-H groups of PBI and the sulfonate groups of SPS-Na. The disruption of PBI chains self association owing to the interaction between the functional groups of these polymer pairs is the driving force for the blending. Thermodynamical studies carried out by using differential scanning calorimeter (DSC) establish partially miscible phase separated blending of these polymers in a wider composition range. The two distinguishable glass transition temperatures (T(g)) which are different from the neat components and unaltered with the blends composition attribute that the domain size of heterogeneity (d(d)) of the blends is >20 nm since one of the blend component (SPS-Na particle) diameter is ∼70 nm. The diminish of PBI chains self association upon blending with SPS-Na particles and the presence of invariant T(g)'s of the blends suggest the wrapping of PBI chains over the SPS-Na spherical particle surface and hence resulting a core-shell morphology. Transmission electron microscopy (TEM) study provides direct evidence of core-shell nanoparticle formation; where core is the polystyrene and shell is the PBI. The sulfonation degree affects the blends phase separations. The higher degree of sulfonation favors the disruption of PBI self association and thus forms partially miscible two phases blends with core-shell morphology.