S. Fendorf et al., Chromium transformations in natural environments: The role of biological and abiological. processes in chromium(VI) reduction, INT GEOL R, 42(8), 2000, pp. 691-701
Chromium is a redox-dynamic element that has many industrial uses. As a con
sequence, it is often introduced at elevated levels into the surface enviro
nment through human activity. Additionally, ultramafic rocks such as serpen
tinite are commonly enriched in chromium, and thus can also lead to appreci
able levels of this element within soils and waters. In the trivalent state
, it poses little hazard to biological activity, but, unfortunately, in the
hexavalent state it is very toxic, to living matter. One must;therefore as
sess the oxidation state of Cr in a given system and determine the potentia
l for transformation between valence states. The objective of this paper to
is review and provide new insight on reduction reactions of Cr(VI) within
natural environments. A number of aerobic and anaerobic bacteria demonstrat
e the enzymatic ability to reduce Cr(VI) to Cr(III); two species can even g
row using Cr(VI) as the terminal electron acceptor in respiration. The abil
ity to reduce chromium in itself is not evidence that the process will take
place at appreciable levels in natural environments, however. Reduced mate
rials such as ferrous iron or hydrogen sulfide may compete with biological
pathways in the reduction of Cr(VI). On the basis of measured reaction rate
s and derived rate expressions, we demonstrate that biological pathways are
not likely to contribute to the reduction of chromate in anaerobic systems
. Ferrous iron will dominate the reduction of chromate at pH values greater
than similar to 5.5, whereas hydrogen sulfide will dominate at pH values b
elow this value. In contrast, bacteria may be the principal means by which
Cr(VI) is converted to Cr(III) in aerobic environments. Thus, the process b
y which Cr(VI) is reduced will depend primarily on the aeration status of t
he system, and secondarily on pH and the concentrations of specific reduced
phases.