Non-exponential patterns are well known characteristics of relaxations
in glassy systems; however, the origin of dispersion is a matter of d
ebate in many cases. Dielectric relaxation and solvation dynamic data
are compared along the lines of the mean spherical approximation theor
y for discriminating between homogeneous and heterogeneous nature of d
ispersion for a low molecular weight glass at 3 K above the glass tran
sition temperature, T-G. From the theoretical point of view, the neces
sary spatial component stems from the dependence of solvation dynamics
on epsilon(omega, k), rather than the macroscopic limit epsilon(omega
, k = 0). It is shown that the two origins of dispersion can be distig
uished in terms of solvation data which agree with the homogeneous lim
it.