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Differential kinematics are not among our reproduced cell characteristics, due to the absence of local adhesions in our model (see the Discussion).
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Our models reproduced observed temporal and spatial distribution of TP and chla well.
Our method reproduced map consistency results for ten runs with a variance of ± 0.3 m.
Furthermore, our model reproduced a two-step recovery, a rapid initial recovery followed by a slow one.
Our model reproduced this dependence on indicator concentration.
Thus, our methodology reproduced both the fission [5], [6] and fusion [7] illusions (see Figure 1).
For example, our model reproduced the experimental results of Guadalupe et al. (2010) [ 90].
Our simulations reproduced similar patterns to experimental data and available information from the literature.
Our model reproduced the entire female population invited into the programme during the period 1996 2011.
Our model reproduced fairly well previously reported experimental data on the number of DSBs and cell survival curves.
Our model reproduced common experimental observations on heterosis using only biologically justified parameters, such as mutation rates.
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