Articles | Volume 10, issue 12
Biogeosciences, 10, 7863–7875, 2013
Biogeosciences, 10, 7863–7875, 2013

Research article 03 Dec 2013

Research article | 03 Dec 2013

Comparative studies of pelagic microbial methane oxidation within the redox zones of the Gotland Deep and Landsort Deep (central Baltic Sea)

G. Jakobs, G. Rehder, G. Jost, K. Kießlich, M. Labrenz, and O. Schmale G. Jakobs et al.
  • Leibniz Institute for Baltic Sea Research Warnemünde (IOW), Rostock, Germany

Abstract. Pelagic methane oxidation was investigated in dependence on differing hydrographic conditions within the redox zone of the Gotland Deep (GD) and Landsort Deep (LD), central Baltic Sea. The redox zone of both deeps, which indicates the transition between oxic and anoxic conditions, was characterized by a pronounced methane concentration gradient between the deep water (GD: 1233 nM, 223 m; LD: 2935 nM, 422 m) and the surface water (GD and LD < 10 nM). This gradient together with a 13C CH4 enrichment (δ13C CH4 deep water: GD −84‰, LD −71‰; redox zone: GD −60‰, LD −20‰; surface water: GD −47‰, LD −50‰; δ13C CH4 vs. Vienna Pee Dee Belemnite standard), clearly indicating microbial methane consumption within the redox zone. Expression analysis of the methane monooxygenase identified one active type I methanotrophic bacterium in both redox zones. In contrast, the turnover of methane within the redox zones showed strong differences between the two basins (GD: max. 0.12 nM d−1, LD: max. 0.61 nM d−1), with a nearly four-times-lower turnover time of methane in the LD (GD: 455 d, LD: 127 d). Vertical mixing rates for both deeps were calculated on the base of the methane concentration profile and the consumption of methane in the redox zone (GD: 2.5 × 10–6 m2 s−1, LD: 1.6 × 10–5 m2 s−1). Our study identified vertical transport of methane from the deep-water body towards the redox zone as well as differing hydrographic conditions (lateral intrusions and vertical mixing) within the redox zone of these deeps as major factors that determine the pelagic methane oxidation.

Final-revised paper