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The pCF algorithm nicely detects a considerable lengthening of the time of the maximum when two positions across NE are correlated (maximum of correlation in the 100 500 ms range).
In case of partial occlusion, the maximum of correlation may be rather far from the actual center of the tomato.
Given that a cell elongates in the direction of motion with a time delay of τ after cell movement, iaCF exhibits the maximum of correlation at Δt = τ.
For each calculated pCF pixel = distance) we selected the time-value corresponding to the maximum of correlation (peak of the pair correlation curve).
Generally, we observed significant variations in the position of the peak of correlation among different experiments (particularly in those across NE) and a broad distribution of transit times around the maximum of correlation in each experiment.
As previously demonstrated [19], we reported the predicted anti-correlation at short time for spatial separations larger than the beam waist, the expected decrease of the overall amount of correlation as a function of distance and the existence of a maximum of correlation at a distance corresponding to the average time necessary to reach that location.
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The location of the maximum and minimum of correlation with unemployment are shifted slightly to 12pm and 12am, though exactly with opposite signs ((0.30pm0.02) for 12am and (-0.38pm0.02) for 12pm).
The maximum values of correlation coefficient for SSeff and CODeff were 0.75 and 0.92, respectively.
The maximum values of correlation coefficient for SSeff, CODeff, and pHeff were 0.96, 0.93, and 0.95, respectively.
The peak of f i j,k (t) is at the time when m i,k and m j,k have maximum number of correlation, namely at the time τ i j,k ≡|τ i,k −τ j,k |.
The dissipation kinetics of lambda-cyhalothrin in tomatoes were determined by plotting the residue concentration against time and the maximum squares of correlation coefficient found were used to determine the equations of best fit curves.
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