While these results demonstrate sufficient sensitivity and specificity of the algorithm, a number of questions arise: Generally, the effects observed in the visual checkerboard experiment are relatively large and regularly observable in the time-series of single trials with the naked eye.
No effect of μg, however, was observed in the visual Nc and in the vestibular Nm which is situated in the close vicinity of the Nd.
This phenomenon has been observed in the visual ventral stream and other sensory modalities, suggesting that it is a common feature of neuronal processing.
Theoretical neuroscientists have long been intrigued by the spatial patterns of neuronal selectivities observed in the visual cortices of many mammals, including primates.
While these experiments did not reveal an overall hand difference for self-recognition, the last study, with improved design and controls, suggested a right-hemisphere advantage for self-compared to other-voice recognition, similar to that observed in the visual domain for self-faces.
In resting conditions, 11C-DAG uptake was observed in the visual association area, and increased in the whole brain and the occipital areas after arecoline stimulation.
The denoising step and the mean fusion process noticeably reduce image noise and properly restore high-frequency information, as observed in the visual comparison in Fig. 16.
Fig. 1 (Modified from Bosking et al. [7].) An Orientation Preference Map observed in the visual cortex of a tree shrew.
Apparent motion has been observed in the visual, auditory, and tactile modalities, given the respective physical stimuli.
Although the results of Experiments 1 and 2 were qualitatively very similar, one difference was quite apparent: larger biases were observed in the visual experiment (Figure 7).
In the auditory intersensory condition, a compression of duration was observed and as can be seen in Figure 6, an increase of variance was observed that did not significantly differ from that observed in the visual test condition.
