Three different aquatic environments (one deep meromictic lake, Lake Lugano
, CH; one shallow meromictic lake, Paul Lake, U.S.A.; and one peat-land cro
ssed by a river, Vallee des Fonts, CH) were studied. The physicochemical ch
aracteristics of hydrous iron oxides identified in these systems were deter
mined by spatially resolved analytical electron microscopy at the level of
individual submicrometric particles. High molecular weight natural organic
matter, dominantly polysaccharides (lakes) or humics (peat-land), serves as
a template for the formation and growth of these particles and governs the
ir final morphology. Depending on the waters, networked microgranules, ill-
defined entities, or quasi-spherical globules were identified. These Fe-C-r
ich particles also contain large proportions of other elements (e.g., P, Ca
, Si); they are thus fundamentally different from pure synthetic iron oxide
s used in the laboratory to infer their transport and sorptive properties.
We show that the morphotypes of aquatic iron oxides are influenced by the c
ombined effect of basic environmental parameters, e.g., the ionic strength,
the relative concentrations of total iron and organic matter, the nature o
f the organic matter, and to a lesser extent the pH in the waters.