Iron in northern Australian shelf waters was found predominantly in fi
ne (< 0.2 mu m) 8-hydroxyquinoline-reactive form or in larger (> 1.0 m
u m) particulate form. Partitioning into the larger size fraction domi
nated during a period of high turbidity following a cyclonic resuspens
ion event. Only a small component of the iron pool reacts rapidly with
the strong ferrous binding agent ferrozine. The concentration of the
ferrozine-reactive component is strongly dependent on light intensity
with maximum concentration observed at peak light intensity. The close
correlation between ferrozine-reactive iron concentration and light i
ntensity suggests a fine balance between Fe(III) reduction and Fe(II)
oxidation with the steady state concentration observed being strongly
influenced by light induced changes in redox kinetics. An observed lac
k of association between particulate iron concentrations and the conce
ntration of ferrozine-reactive iron suggests that the soluble rather t
han the particulate iron pool is most influenced by light. The chromop
hore may be an Fe(III)-organic complex with the strong iron binding li
gand that is now recognised to be present in seawater.