Affiliation:
1. School of Biological Sciences, Queen Mary, University of London, London E1 4NS, United Kingdom
Abstract
ABSTRACT
Until recently, denitrification was thought to be the only significant pathway for N
2
formation and, in turn, the removal of nitrogen in aquatic sediments. The discovery of anaerobic ammonium oxidation in the laboratory suggested that alternative metabolisms might be present in the environment. By using a combination of
15
N-labeled NH
4
+
, NO
3
−
, and NO
2
−
(and
14
N analogues), production of
29
N
2
and
30
N
2
was measured in anaerobic sediment slurries from six sites along the Thames estuary. The production of
29
N
2
in the presence of
15
NH
4
+
and either
14
NO
3
−
or
14
NO
2
−
confirmed the presence of anaerobic ammonium oxidation, with the stoichiometry of the reaction indicating that the oxidation was coupled to the reduction of NO
2
−
. Anaerobic ammonium oxidation proceeded at equal rates via either the direct reduction of NO
2
−
or indirect reduction, following the initial reduction of NO
3
−
. Whether NO
2
−
was directly present at 800 μM or it accumulated at 3 to 20 μM (from the reduction of NO
3
−
), the rate of
29
N
2
formation was not affected, which suggested that anaerobic ammonium oxidation was saturated at low concentrations of NO
2
−
. We observed a shift in the significance of anaerobic ammonium oxidation to N
2
formation relative to denitrification, from 8% near the head of the estuary to less than 1% at the coast. The relative importance of anaerobic ammonium oxidation was positively correlated (
P
< 0.05) with sediment organic content. This report of anaerobic ammonium oxidation in organically enriched estuarine sediments, though in contrast to a recent report on continental shelf sediments, confirms the presence of this novel metabolism in another aquatic sediment system.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
302 articles.
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