847spectrum of the azonaphthol shows a prominent molecular ion a t mle 316. When the experiment was run by using 15N labeled sodium nitrate, the molecular ion was then observed a t mle 317. A substantial peak at M -1 indicated that hydrogen loss is a major route for the molecular ion of the azonaphthol, but after correction for this, the azonaphthol was found to incorporate one I5N essentially quantitatively. This shows that one nitrogen atom in the azonaphthol originates with the NaNO3 Since the baderia were shown to reduce nitrate to nitrite, this result provides additional confirmation for the diazonium ion pathway proposed in our previous paper (Corke et al., 1979) for the microbial transformations of anilines under anaerobic conditions. Further studies are in progress to determine (1) the genesis of the other compounds (triazenes, azobenzenes and biphenyls) and (2) whether these model systems are operative in soils. LITERATURE CITED Bartha, R. J. Agric. Food Chem. 1968, 16, 602.