Effect of increased sulfate reduction on the stability of authigenic vivianite in lake sediment
- 1Leibniz Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 301, 12587 Berlin, Germany
- 2Brandenburg University of Technology Cottbus-Senftenberg, Platz der Deutschen Einheit 1, 03046 Cottbus, Germany
The presence of high levels of phosphorus (P) in surface waters can negatively impact the functioning of ecosystems and water quality. Despite efforts to decrease P concentrations, the accumulation of P reservoirs in sediment from past high external inputs still poses a problem. This legacy P can contribute to internal P loading, which has been shown to extent eutrophication in many freshwater systems. To effectively restore these systems, it is important to understand the geochemical processes that control the fixation and release of P in the sediment. While it is known that under anoxic conditions, P can be stored in the form of the mineral vivianite, it is not well understood if the vivianite reservoir can also act as a source of P. In a field study, mixed sediment from Lake Arendsee, Germany that naturally contained vivianite was placed in the sediment floor of the same lake, in both sulfate reduction depths and below (0-45cm). After three months, the sediment was retrieved and analyzed to investigate the effect of sulfide production on the vivianite pool. Sequential extraction and XRD analysis of the sediment solid phase showed that at shallower depths where sulfide concentrations were higher, there was a significant reduction of the vivianite reservoir and a decrease of P bound to Fe relative to S bound Fe forms. This suggests that P bound in vivianite can act as a P source in sulfidic sediment. Further research is needed to determine the extent of this phenomenon in lakes with increased sulfide production.
How to cite: van Kuppevelt, H. and Hupfer, M.: Effect of increased sulfate reduction on the stability of authigenic vivianite in lake sediment , EGU General Assembly 2023, Vienna, Austria, 24–28 Apr 2023, EGU23-17209, https://doi.org/10.5194/egusphere-egu23-17209, 2023.