Plots of avian and conspecific photon catches of P. erhardii coloration and their corresponding natural backgrounds in tetrahedral color space showed that, in all 3 body regions (ventrolateral flanks, upper backs, and lower backs), the distribution of relative stimulation of avian predator and conspecific cones occupied distinct regions in color space.
The temperature distributions of steam stimulation and HDCS stimulation are shown in Figs. 4 and 5, respectively.
It implied that not only the energy level but also the energy distribution of the stimulations in the environment affects our perceptions.
We analyzed the time-frequency energy distribution of the stimulation-evoked response by continuous wavelet transformation [49].
Yu et al. [ 114] studied the cellular distribution of nucleolin after stimulation with ECM proteins, and report that, following laminin stimulation, nucleolin translocates from the cytoplasm to the nucleus and stimulates cell proliferation.
Overall, this study demonstrates the feasibility of TRMM rainfall data (whether original or bias-corrected) which can reflect the spatial distribution of rainfall in streamflow stimulation at data-sparse area of Laos, although the daily flow simulation results are not that satisfactory.
The Objectives of this study are to characterize the distribution of pain provoked by stimulation at the C1-3 levels, and to investigate the potential efficacy of a novel, brief low temperature radiofrequency rhizolysis (BLT-RF) as a therapy for patients with occipital neuralgia.
Treatment of the HeLa cells with ionomycin or with BAPTA-AM did not significantly modify these localizations, and did not modify the cytoplasmic distribution of Lad1 upon EGF stimulation.
Possibly these variations, and the occurrence and distribution of responses to cortical stimulation, could be predicted.
On the other hand, if one could predict occurrence and distribution of responses to cortical stimulation, then this might be used therapeutically.
