Temporal phenotypic variation of spinach root traits and its relation to shoot performance.

The root system is important for the growth and development of spinach. To reveal the temporal variability of the spinach root system, root traits of 40 spinach accessions were measured at three imaging times (20, 30, and 43 days after transplanting) in this study using a non-destructive and non-invasive root analysis system. Results showed that five root traits were reliably measured by this system (RootViz FS), and two of which were highly correlated with manually measured traits. Root traits had higher variations than shoot traits among spinach accessions, and the trait of mean growth rate of total root length had the largest coefficients of variation across the three imaging times. During the early stage, only tap root length was weakly correlated with shoot traits (plant height, leaf width, and object area (equivalent to plant surface area)), whereas in the third imaging, root fresh weight, total root length, and root area were strongly correlated with shoot biomass-related traits. Five root traits (total root length, tap root length, total root area, root tissue density, and maximal root width) showed high variations with coefficients of variation values (CV ≥ 0.3, except maximal root width) and high heritability (H2 > 0.6) among the three stages. The 40 spinach accessions were classified into five subgroups with different growth dynamics of the primary and lateral roots by cluster analysis. Our results demonstrated the potential of in-situ phenotyping to assess dynamic root growth in spinach and provide new perspectives for biomass breeding based on root system ideotypes.

Low-frequency mechanical spectroscopy study of conformational transition of polymer chains in concentrated solutions.

A low-frequency mechanical spectroscopy approach for liquids was proposed for studying conformational transition of polymer chains in concentrated solutions. The technique is applied to aqueous solutions of a poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) triblock copolymer in order to determine if chain conformation is altered in response to temperature. Two transitions are revealed by mechanical spectra and verified by differential thermal analysis with increasing temperature, which may be related to the unimer-to-micelle transition and the phase separation, respectively. The transitions are also found to be much dependent on the concentration of the solution and the addition of NaCl. Moreover, it reveals that the PEO blocks play a more important role in the micellar crystallization process. This study may be helpful in understanding the dynamics of polymer chains in concentrated solutions.