Measurements of (13)CH(4)/(12)CH(4) and (12)CH(3)D/(12)CH(4) ratios in atmospheric methane (CH(4)) sources provide important information about the global CH(4) budget as well as about CH(4) production and consumption processes occurring within the various sources. As an alternative to the conventional mass spectrometer (MS) technique, which requires conversion of CH(4) to CO(2) and H(2), we have developed a tunable diode laser absorption spectrometer (TDLAS), which permits rapid direct measurements of the (13)CH(4)/(12)CH(4) and (12)CH(3)D/(12)CH(4) ratios. An intercomparison between TDLAS and MS techniques for samples from natural wetlands, landfills, and natural gas sources resulted in a mean deviation of Δδ(13)C = 0.44‰ and ΔδD = 5.1‰. In the present system the minimum mixing ratios required are 50 parts in 10(6) by volume (ppmv) CH(4) (sample size 2 µmol CH(4)) for direct δ(13)C measurements and 2000 ppmv (sample size 80 µmol CH(4)) for direct δD measurements. These mixing-ratio limits are adequate for most CH(4) source characterization studies without requiring sample preconcentration.