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Our results demonstrate that generally the critical migration rate increases with increasing selection coefficient s.
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Some smaller bubbles that form above the hydrophilic surfaces have the tendency to migrate to the neighboring plain surfaces and combine with the existing bubbles, and the migration rate increased in conjunction with the temperature; this intensified bubble accumulation forced the unstable bubble to break off from the plain surfaces, thereby producing an upward surge of flow.
The migration rate increased with an increase in concentration from 1 to 10 μg/mL, and then showed an inverse correlation as the migration rate declined as the concentration increased from 10 μg/mL (Fig. 4b).
Their migration rates increased initially and then decreased along with the increase of mPEG grafting mass.
Columns 1 3 of Table 7 show that no matter the way we specify the incidence of relative unemployment in origin and destination country, migration rates increase whenever the stock of migrants is higher at destination.
Finally, when pollen migration rates increased (Nm = 10.2 vs Nm = 5.1), no significant change was observed in the slopes of the clines.
18 h after treatment with 10 µM LPA, the cell migration rate was increased significantly by 234.55±27.31% compared with control cells without LPA treatment.
In combination with constantly improving estimation procedures, it is now feasible to estimate these parameters, like effective population size, inbreeding coefficient and migration rate, with increasing accuracy.
Consistent with this view, Figure 4 shows that the linear regime of periodic selection is extended to a larger parameter range as the long-range migration rate is increased.
In this instance, migration rates have increased in part because of the substantial health risks associated with famine.
When migration rates are increased, the inferred population size quickly approaches the total population size (in this case ).
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CEO of Professional Science Editing for Scientists @ prosciediting.com