The fate of ammonium in anoxic manganese oxide-rich marine sediment

Citation
B. Thamdrup et T. Dalsgaard, The fate of ammonium in anoxic manganese oxide-rich marine sediment, GEOCH COS A, 64(24), 2000, pp. 4157-4164
Citations number
54
Categorie Soggetti
Earth Sciences
Journal title
GEOCHIMICA ET COSMOCHIMICA ACTA
ISSN journal
00167037 → ACNP
Volume
64
Issue
24
Year of publication
2000
Pages
4157 - 4164
Database
ISI
SICI code
0016-7037(200012)64:24<4157:TFOAIA>2.0.ZU;2-A
Abstract
The possibility for anaerobic NH4+ oxidation and N-2 formation was explored in a Mn oxide-rich continental basin sediment from Skagerrak. The surface sediment contained 2.9 weight-% Mn(IV), and reactive Mn oxide persisted to greater than or equal to 10 cm depth. Microbial Mn reduction completely dom inated anaerobic carbon oxidation, whereas neither Fe reduction nor sulfate reduction were significant. Accumulation rates of soluble NH4+ during anox ic incubations scaled with Mn reduction rates and did not indicate any subs tantial oxidation of NH4+. No sustained production of N-15-labelled N-2 fro m added (NH4+)-N-15 was detectable during the four-day incubations, which c onstrains the rate of NH4+ conversion to N-2 to <2% of the NH4+ production rate. Traces of N-15-labelled N-2 accumulated initially, and this transient N-2 production was possibly related to brief coupled nitrification/denitri fication resulting from sediment handling. Oxidation of NH4+ to NO3- was al so insignificant as there was no accumulation of NO3- during the incubation s and added (NO3-)-N-15 was rapidly consumed with N-2 as a major product. A lthough the oxidation of NH4+ with Mn oxide is thermodynamically favorable, our results demonstrate that such oxidation was insignificant and that NH4 + can be considered the end product of nitrogen mineralization in this anox ic Mn oxide-rich sediment. Copyright (C) 2000 Elsevier Science Ltd.