Let
s be the retinal size and
c be the retinal contrast of an object. To explain our results, we suggest that when the in-depth motion happens, the brain first scales
s and
c by the same dimensionless factor
k, which is some function of the relative depth
d/
d 0:
Here,
d 0 stands for the reference depth wherefrom the motion started, while
S and
C stand for the perceived size and contrast, respectively. Based on the data plotted in
Figure 3, function
k(
) is approximately linear for small motion amplitude factors and is decelerating for large amplitude factors. In addition, result (ii) in the
Discussion section indicates that the retinal size,
s, contributes to the perceived contrast,
C, to the same degree as the retinal contrast,
c. In addition, results (i) and (iv) indicate that the perceived size,
S, and perceived contrast,
C, are not symmetrical. Both these facts can be accommodated into the model by one simple modification of the contrast relationship:
where
S(
d 0) is the perceived size at the starting depth
d 0 and
S(
d) is the perceived size at the current depth
d. In other words, the perceived contrast is additionally scaled by the relative perceived size
. This model is illustrated by the diagram in
Figure 9. Note that the perceived-size scaling factor equals 1 for the ecologically important case of size constancy (objects of constant size) where, presumably,
S(
d) =
S(
d 0) for any
d. Thus, in order to calculate the perceived size and contrast for the size constancy condition, the retinal contrast and size are scaled by the same depth factor
k.