To analyze the thermorheological behavior of various polyethylenes, the relaxation spectra were shifted. Not only linear and short-chain branched PE but also the classical high-pressure LDPE were found to be thermorheologically simple, i.e., the activation energy E-a is independent of the relaxation strength or the relaxation time, respectively. However, for the long-chain branched metallocene catalyzed polyethylenes investigated a significant dependence of the activation energy E-a on the relaxation time is detected. At shorter relaxation times E-a is very close to that of linear PE, but it increases with longer times. The lower E-a values are assumed to be due to linear molecules and the higher ones to different species of long-chain branched molecules. These findings offer the possibility to use the analysis of the thermorheological complexity to get an insight into the branching structure of polyethylenes. For the LCB-mPE investigated, it can be concluded that they are a mixture of linear and long-chain branched chains.