The impact of electrogenic sulfide oxidation on elemental cycling and solute fluxes in coastal sediment

Rao, Alexndra M.F.; Malkin, Sairah Y.; Hidalgo-Martinez, Silvia; Meysman, Filip J.R.

doi:10.1016/J.GCA.2015.09.014

Title

The impact of electrogenic sulfide oxidation on elemental cycling and solute fluxes in coastal sediment

Author

Rao, Alexndra M.F.

Malkin, Sairah Y.

Hidalgo-Martinez, Silvia

Meysman, Filip J.R.

Abstract

Filamentous sulfide oxidizing cable bacteria are capable of linking the oxidation of free sulfide in deep anoxic layers of marine sediments to the reduction of oxygen or nitrate in surface sediments by conducting electrons over centimeter-scale distances. Previous studies have shown that this newly discovered microbial process, referred to as electrogenic sulfide oxidation (e-SOx), may alter elemental cycling in sediments, but the nature and rates of the resulting biogeochemical transformations and their influence on benthic-pelagic coupling remain largely unknown. Here we quantify changes in sediment geochemistry and solute fluxes at the sedimentwater interface as e-SOx develops and declines over time in laboratory incubations of organic-rich sediments from a seasonally hypoxic coastal basin (Marine Lake Grevelingen, The Netherlands). Our results show that e-SOx enhanced sediment O2 consumption and acidified subsurface sediment, resulting in the dissolution of calcium carbonate and iron sulfide minerals in deeper sediment horizons and the associated accumulation of dissolved iron, manganese, and calcium in porewater. Remobilized Fe diffusing upward was reoxidized at the sedimentwater interface, producing an amorphous Fe oxide crust, while dissolved Fe diffusing downward was reprecipitated in the form of FeS as it encountered the free sulfide horizon. The development of e-SOx enhanced the diffusive release of dissolved Mn at the sedimentwater interface, capped the phosphate efflux, generated a buildup of organic matter in surface sediments, and strongly stimulated the release of alkalinity from the sediment. About 75% of this alkalinity production was associated with net CaCO3 dissolution, while the remaining 25% was attributed to a pumping mechanism that transfers alkalinity from anodic H2S oxidation (an alkalinity sink) in deeper sediments to cathodic O2 reduction (an alkalinity source) near the sedimentwater interface. The resulting sediment alkalinity efflux buffers the release of dissolved inorganic carbon at the sedimentwater interface, and may therefore counteract the influence of benthic respiration on coastal ocean pH. Overall, our results demonstrate that e-SOx development strongly affects the biogeochemical cycles of C, P, Ca, Fe, Mn, and S in coastal sediments.

Language

English

Source (journal)

Geochimica et cosmochimica acta. - Oxford, 1950, currens

Publication

Oxford : 2016

ISSN

0016-7037 [print]

1872-9533 [online]

DOI

10.1016/J.GCA.2015.09.014

Volume/pages