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It should be noted from Fig. 5 that at χ = 0.9, the evolution of length with time is erratic because of the non-monotonic trend of the etch rate at the tip (see Additional file 1: Figure S5b).
We show of Appendix figure 3 the evolution of length after a blebbistatin treatment at time = 0 min. 10.7554/eLife.09206.018 Appendix figure 2. Stretch of the cell during the ring migration.
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However, given our results, we suggest that, in general, more distal COM positions seem to drive variation in stride lengths across taxa, and the evolution of stride length variation is likely tied to morphological variation.
To allow for the evolution of proboscis length, the genome of moths must include a number of loci that determine proboscis length.
It thus appears that the evolution of intron length and genome size may be uncoupled in plants or alternatively, that the evolution of intron length is lineage specific.
Special attention is given to the evolution of the length of hedges.
We then studied the evolution of the length of their major and minor axes for the entire agriculture season.
On the composites, reinforcing effects have been observed according to the evolution of fibre length and fibre content.
In Fig. 7e, the black squares, blue stars, and red circles show the evolution of NW length, base diameter, and tip diameter as functions of the growth duration.
These mechanisms are implemented in a phenomenological equation governing the evolution of rod length, with the number density of rods appropriately modified to ensure conservation of surfactant mass.
During uniaxial compression, the evolution of this length caused by different conditions, such as annealing, hydrostatic pressure, power-law creep, diffusion and grain boundary sliding (GBS), was estimated.
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