The complexation of U(VI) with Aldrich humic acid (HA) was studied at pH 7 under exclusion of CO 2 . Using two independent laser-induced spectroscopic methods, timeresolved laser-induced fluorescence spectroscopy (TRLFS) and TRLFS with ultrafast pulses (fs-TRLFS), the formation of the ternary U(VI) mono hydroxo humate complex UO 2 (OH)HA(I) by reaction of UO 2 OH + with HA was studied. Assuming that all proton exchanging functional groups of the HA are able to contribute to the complex formation, a mean stability constant of 6.58 ± 0.24 was derived for UO 2 (OH)HA(I). Alternatively, the analytical data were evaluated based on the metal ion charge neutralization model resulting in a complexation constant of 6.95 ± 0.10 and a loading capacity of 0.76 ± 0.28. An overall complexation constant of log β 0.1 M = 14.89 ± 0.54 was calculated for the total reaction of U(VI) with HA starting from the non-hydrolyzed UO 2 2+ ion. This value agrees very well with literature data. Taking into account the UO 2 (OH)HA(I) complex, the speciation of U(VI) in presence of HA was recalculated. It was found, that the formation of UO 2 (OH)HA(I) can significantly influence the U(VI) distribution in the environmentally relevant pH region. As a consequence, the mobility of U(VI) in natural aquifer systems could be enhanced.