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The means +/− standard error (error bars) were determined for all appropriate data.
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(A ) For each gene the ratio of mRNA levels (red bars) and translation efficiency (TE) (blue bars) was determined for G2 vs M (left) or G2 vs G1 (middle) and M vs G1 (right).
The error bars were determined by the extensive observation on more than 25 QDs for each data point.
Horizontal error bars were determined by computing the standard errors of the CFU counts for each agar-plated inoculum titer after a three week incubation period.
Vertical error bars were determined by computing the standard errors using the data points remaining for each inoculum.
Beam curvatures, strain in reinforcing bars and shear deformations were determined for each specimen based on experimental measurements to obtain local response quantities.
The amounts of mercury (A; ng/plant, B; ng/fresh weight) that accumulated in wild-type plants (Wild; empty bar) and merE- transgenic plants (black bar) were determined after culture for 2 weeks on MS gellan gum plates with various concentrations of HgCl2 or CH3HgCl, as described in the Materials and Methods.
By dividing the repression ratio for protein production and that for mRNA concentration, the repression ratio for translation efficiency (protein yield per mRNA molecule, white bars) was determined.
The on-board performance and high-volume manufacturing cost were determined for compressed hydrogen tanks with design pressures of 350 bar (∼5000 psi) and 700 bar (∼10,000 psi) capable of storing 5.6 kg of usable hydrogen.
So far, the inner-level part is solved and (bar {f} tau)) is determined for any given τ.
As a result, the optimum ratio of steel fibers to shear-reinforcing bars for the shear-load capacity is determined for the RSF linear members.
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