Samples from the Scandinavian NOM-typing set were studied by total luminesc
ence spectroscopy (TLS). All samples showed fluorescence spectra typical fo
r NOM of aquatic origin, or fulvic acids from both aquatic and terrestrial
sources, but were lacking additional features typical for humic acid and le
af litter extract spectra. A comparison of the NOM spectra from the same so
urce, but isolated by different methods, suggests that the reversed osmosis
isolation procedure removes a small percentage of all fluorescing compound
s when compared to the evaporation procedure. Spectral differences between
NOM samples of different age suggest reduction of the more highly conjugate
d aromatics with increasing residence time in the water either by precipita
tion or by biodegradation to simple phenolics. NOM samples were spiked with
aluminium, which led to pronounced qualitative changes in the NOM TLS. The
most prominent change was the appearance of a shoulder at lambda(ex)/lambd
a(em) = 350/375. The fluorescence intensity at this wavelength pair was fou
nd to be positively correlated with inert and "bound" Al, as determined by
fast reaction with 8-hydroxyquinoline and capillary electrophoresis, respec
tively. (C) 1999 Elsevier Science Ltd.