To produce timely responses, animals must conquer delays from visual pro cessing pathway by predicting motion. Previous studies [1] revealed that predic tive information of motion is encoded in spiking activities of retinal ganglion cells (RGCs) early in the visual pathway. In order to study the predictive properties of a retina in a more systematic manner, stimuli in the form of a stochastic moving bar are used in experiments with retinas from bull frogs in a multielectrode sys tem. We then investigated the predictive properties of single RGC by calculating the time shifted (δt) mutual information (MI(x,r;δt)) between spiking output (r(t)) from a single RGC and the bar trajectories (x(t)). Two kinds of cells are charac terized: predictive RGCs and nonpredictive RGCs. In order to further understand the mechanism of prediction, we develop a negative group delay model which is based on Voss's [2] paper to generate anticipatory responses. We extend our model to spatial version and use the same stimulation condition as we use in experiments. The model indicates that delayed negative feedback is crucial for producing antic ipation dynamics. Besides, we also show feedforward inhibition can also generate similar prediction dynamics. Besides, our feedback and feedforward model can also predict constant velocity moving bar [3]. After adding LPOU noises into con stant velocity moving bar, our model even predicts better than Berry gain control model [3] which explains anticipation of constant velocity moving bar. To sum up, our feedback and feedforward model can anticipate both stochastic and constant velocity moving bar with and without noises.