This is consistent with multiple representations, because a single representation would predict perfect performance at all orientations following exposure at a single orientation.
For each condition, both the initial responses to the superposition as well as the second response to a single orientation were represented by peaks of activity that were separated in time with longer switch delays (dark gray area).
The observations also showed large in-grain misorientations sometimes as large as 25°, while the model assumes a single orientation for each grain.
Each crossover point is itself topologically a four-arm junction, but is constrained to a single orientation, as opposed to the flexible single four-arm junction, providing a rigidity that makes the DX motif suitable as a structural building block for larger DNA complexes.
In the result of t 1,t 2, the angle is identical to −t 1,−t 2; however, the orientation is 180° opposite as in Fig. 2. While making a single orientation, (θ is on the first/fourth quadrant), when the result is t1 <0, θ + π is the only orientation of ϕ that rotates the embedded binary image clockwise towards the only orientation, and this phenomenon is referred to as discrete rotation.
Experimentally, this orientation plasticity is induced by exposure of young animals to retinal images restricted to a single orientation [9] [16].
High activity of multiple orientations leads to a suppression of overall cell activity whereas activity in a single orientation channel leaves cell activity relatively unchanged.
A change from superimposed orientations to a single orientation has 2 underlying constituents: A switch from one orientation to blank (off-component), and an overlaid continuous presentation of the orthogonal orientation (sustained, adaptive component).
A single orientation of a single crystallite can therefore produce scattering from a large range of hkl reflections.
When a gene is active on only a single strand, the corresponding RNA is expressed in a single orientation.
