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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.
In a comparative framework, the hypothetical increase in the rate of evolution of tibia length due to the absence of genetic correlation would produce relative tibia length equivalent to the kangaroo rat in fewer than 40 generations.
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.
Fig. 5 Evolution of SiNW length with time for different HF H2O2 molar ratios at 48 M H2O. a Effect of etch time on SiNW length.
Special attention is given to the evolution of the length of hedges.
Fig. 6 Evolution of SiNW length with time for different H2O concentrations at a fixed HF H2O2 molar ratio of 0.95.
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.
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