Higher thermal response amplitude associated with disrupted heat transfer was observed where localized spallation at or near the YSZ/TGO interface occurred.
Moreover, previous studies mostly employed either an auditory task or passive listening to salient sound stimuli to obtain sufficiently high evoked response amplitudes.
At the population level, response amplitude with high contrast stimuli was significantly (p<0.0001) lower after adaptation to high contrast compared to adaptation to mixed contrasts (median percent change: 91.3%).
Based on the definitions of DNL, ADNL, and PNL, all parameters characterize one feature of soil nonlinearity, that is, the reduction in the site response amplitude at high frequency.
This can produce easy-to-detect changes in response amplitude with high sensitivity to structural change, but requires resonant devices with specific dynamic behavior which is not always easily reproduced.
On the other hand, with low contrast stimuli, response amplitude was higher in the constant contrast condition (Fig. 1C), and the HWHH was broader compared to that in the mixed contrasts condition (15.4 vs. 12.2 deg).
Because response amplitude exhibits high variability between cells, amplitude alone does not provide sufficient information to discriminate an SS versus LL signal.
Figure 4 shows that a slight reduction in the site response amplitude of the high-frequency band could be observed during strong motions.
While high-pass filtering reduces the direct response amplitude and duration, its convolution trace may still exhibit extremely large values (as much as 10 times greater than those of indirect synaptic responses) with long durations.
Overall, BOLD response amplitude was significantly higher for a fixed retinotopic location near the vertical meridian when the gaze direction positioned that location nearer the straight-ahead direction (regions at 6° and 14° of distance from straight-ahead direction).
