We demonstrate the use of transmission electron microscopy (TEM) to study the effects of beta-decay of radioactive 137Cs to 137Ba in crystalline pollucite (CsAlSi2O6). Most prior work on radiation effects in materials has focused on structural damage from alpha radiation. Beta radiation, on the other hand, causes little atomic displacement, but the decay transmutation, that is, the radioactive decay of a radioisotope to an isotope of another element, results in progeny with different the valence and ionic radius. Cesium-137, a fission product of uranium, is a major contaminant at U.S. Department of Energy production facilities. Pollucite is an aluminosilicate ceramic with potential use for long-term storage of 137Cs. We focused on one of several available 137Cs sources originally fabricated in the 1970s and 1980s. These sources were small, sealed, stainless steel capsules containing pollucite in which varying amounts of the natural Cs had been replaced by radioactive 137Cs (t1/2 = 30.13 years). The sample chosen for TEM examination, aged for nearly 20 years, contained the most radiogenic barium and was expected to show the largest radiation effects. Bright field transmission images revealed a homogeneous crystalline matrix, with no evidence of distinct Ba phases or ex-solution phenomena resulting from the 137Cs transmutation. Electron diffraction patterns obtained from several portions of the sample were consistent with literature values for pollucite. These data suggest that little substantial damage was done to the crystal structure of this sample, despite the transmutation of nearly 1.5% of the total cesium to barium over the elapsed 20 years. Although our observations are limited, to our knowledge these are the only available data in which transmutation effects have been isolated from other radiation damage phenomena.