The degradation of melt polyolefin elastomer (POE) at the presence of dicumyl peroxides (DCP) was estimated at elevated temperature in oscillatory shear flow. Large amplitude oscillatory shear (LAOS) experiments followed by Fourier transform rheology (FTR) were carried out to detect and evaluate the branching architecture of the products. The third complex harmonic (I-3*) and other two parameters, small strain elastic shear modulus (M) and large strain elastic shear modulus (L), which describe the nonlinearity and elasticity of a material obtained from FTR, are mainly used to characterize the topological structure of polymer chains. The results indicate the degradation appeared just after a large amount of the long chain branches (LCB) created rather than as soon as the reaction started when the strain was applied within the linear viscoelastic regime of the original POE at high frequencies. This is different from our previous result that the dominant reaction was coupling in linear shear flow. The threshold strain for degradation decreased with the oscillatory frequency, and the frequency owned a different acting mechanism from the strain amplitude to cause the degradation reaction. Moreover, there is a kind of selectivity of shear rate on the polymer chains for degradation. Low frequency results in short linear scission segments and a long branched chain suffers from degradation more than once. At high frequency, the possibility of degradation at the sites near the branching points of LCB increases. (C) 2007 Elsevier Ltd. All rights reserved.