Exact(6)
The peripheral acceleration and deceleration illusions are consistent with the hypothesis that the blurring of multiple sources of motion information occurs in peripheral vision.
The peripheral acceleration illusion (Movies S2) occurs when the motion inside the ovals is faster than the motion of the ovals but in the same direction.
In the peripheral acceleration illusion, both the first- and the second-order systems have significant motion energy in the right-to-left (forward) motion direction.
The displays (referred to as the peripheral escalator illusion, peripheral acceleration and deceleration illusions, rotating reversals illusion, and disappearing squares illusion) create dramatically different perceptions when viewed foveally versus peripherally.
The peripheral acceleration and deceleration illusions consist of ovals that drift from left to right across the screen, and that contain an internal grating moving in the same (acceleration) or opposite (deceleration) direction, and at a faster or slower speed than the motion of the ovals across the screen (see Figs. 3A and 4A; Movies S2 and S3).
Projections of the peripheral acceleration movie in the x-t and y-t planes are shown in Figures 3B and C. Two significant slants in the x-t plane can be seen: the four stripes and their internal patterns, both in the same upper-right to lower-left orientation.
Similar(54)
The peripheral escalator, acceleration and deceleration illusions and rotating reversals illusion all show a similar trend: in the fovea, the first-order motion energy and second-order motion energy can be perceptually separated from each other; in the periphery, the perception seems to correspond to a combination of the multiple sources of motion information.
Acceleration of peripheral arterial vascular disease has been reported with nilotinib in CML patients both with and without other risk factors for CAD [ 33, 34].
This chapter illustrates memory subsystem design including addressing circuitry, memory peripherals, and special addressing circuitry for address acceleration.
One of the mechanisms that is thought to contribute to this acceleration is a corticosterone-induced change in peripheral deiodinating activity.
Coincident histological analyses confirmed the cellular basis of transcriptional changes and highlighted the dramatic acceleration of development in the fovea compared with peripheral retina.
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