Pb isotope data, major and trace element compositions, fission track and synchrotron X-ray fluorescence analyses are presented for staurolites from nine pelitic schists in the continental United States to evaluate their potential use in U-Pb geochronology. Seven U-Pb analyses from Lanzirotti and Hanson (1995) are reexamined with respect to this additional data which was not available at the time. These data are then compared to 21 new U-Pb analyses of staurolite of varying composition from a variety of localities. The primary goals of this study are to: (1) evaluate the variability in U and Pb abundance and U/Pb ratio in staurolites of varying composition; (2) constrain how much of the measured U and Pb is derived from radiogenic solid inclusions such as monazite and zircon; (3) constrain how much of the measured U and Pb is derived from staurolite itself and evaluate any possible correlation of U and Pb abundance and U/Pb ratio to major element composition; (4) place preliminary constraints on closure temperature to Pb diffusion in staurolite; (5) evaluate how meaningful U-Pb ages can better be calculated for the low U/Pb ratio minerals. In the staurolite fractions analyzed U abundances range from 0.2 to 24.9 ppm, Pb from 0.13 to 2.41 ppm, the 238U/204Pb ratios vary from 135 to 9447, and the 206Pb/204Pb ratios from 23 to 623. For many of the fractions analyzed precise U-Pb ages can be calculated (±10 Ma or better) that appear to be consistent with available age constraints on the time of peak metamorphism. Mass balance calculations, fission track analysis, and synchrotron X-ray fluorescence trace element mapping show that although radiogenic inclusions are almost always present in large staurolite porphyroblasts, it is difficult for inclusions to account for the measured Pb isotopic compositions. It is also demonstrated that the U-Pb ages calculated for staurolites from Connecticut are at least 20 Ma older than nearby Rb-Sr muscovite and 40Ar-39Ar hornblende ages. This is consistent with staurolite having a closure temperature to U and Pb diffusion significantly higher than 500 °C.