However, all of the above one-timescale schemes suffer from huge CSI signaling overhead and large computation complexity due to global centralized optimization.
In the preceding example, the bonobo and chimpanzee split a million years ago, suggesting such species' life spans are, like those of the abundant and widespread marine species discussed above, on million-year timescales, at least in the absence of modern human actions that threaten them.
While this observed geometrical difference between the north and the south is qualitatively understandable with the difference in the fault activity in the geomorphological timescale mentioned above, it is quite unclear how this geometrical complexity played roles in determining the resulting slip distribution and surface deformation.
Many of the effects discussed above vary in the timescale over which they act.
Based on the above analysis, we summarize the different timescales on which v evolves in Fig. 15, where the yellow circle indicates the transition point between the slow and superslow timescales that occurs as the trajectory reaches a small neighborhood of (mathscr {M}_{ss}) as it evolves along the lower-v surface of (mathscr {M}_{s}).
For the global ionosphere, the difference in the variation slopes of GEC versus EUV on the two timescales was presented in the above analysis.
As above, we assume that the contribution of each timescale to presynaptic excitability is the same.
As discussed above, reward and punishment affect behavior on multiple timescales.
SO2 abundance has been observed to vary rapidly above the cloud tops on a timescale of ~ an hour (Encrenaz et al. 2013, 2016; Marcq et al. 2011), so variation in contrasts at 283 nm on similar timescales can be expected.
The average cell cycle length after the first cleavage was 21 min, so we corrected the timescale by 20/21, as above.
