The kinetics of water sorption by starch filled polyolefins has been investigated using blends of a commercial starch masterbatch with low density polyethylene (LDPE), high density PE (HDPE), and copolymers of ethylene with methyl acrylate (EMA), ethyl acrylate (EEA), and n-butyl acrylate (EEA). Transient state diffusion coefficients (D) of water in the blends were determined using Fickian analysis of the initial stages of the sorption isotherms. Measured D values were several orders of magnitude lower than values reported for either pure starch or LDPE by various investigators. Resin effects on D were in the order D-HDPE < D-LDPE much less than D-EBA < D-EBA < D-EMA. The resin effects diminished as the starch content increased. The lower magnitude of D in the blends relative to pure LDPE was attributed to the sorption of water by the dry starch particles, in a manner similar to dual-mode sorption in glassy polymers. Copolymer effects were consistent with reduction in crystallinity caused by the comonomers. The dependence of the diffusion coefficient on starch content was not described by mixing models of heterogeneous systems or percolation theory.