Anaerobic oxidation of methane by aerobic methanotrophs in sub-Arctic lake sediments

2017 ◽  
Vol 607-608 ◽  
pp. 23-31 ◽  
Author(s):  
Karla Martinez-Cruz ◽  
Mary-Cathrine Leewis ◽  
Ian Charold Herriott ◽  
Armando Sepulveda-Jauregui ◽  
Katey Walter Anthony ◽  
...  
2019 ◽  
Author(s):  
Guangyi Su ◽  
Jakob Zopfi ◽  
Haoyi Yao ◽  
Lea Steinle ◽  
Helge Niemann ◽  
...  

AbstractAnaerobic oxidation of methane (AOM) by methanotrophic archaea is an important sink of this greenhouse gas in marine sediments. However, evidence for AOM in freshwater habitats is rare, and little is known about the pathways, electron acceptors and microbes involved. Here, we show that AOM occurs in anoxic sediments of a lake in southern Switzerland (Lake Cadagno). Combined AOM-rate and 16S rRNA gene-sequencing data suggest thatCandidatusMethanoperedens archaea are responsible for the observed methane oxidation. Members of the Methanoperedenaceae family were previously reported to conduct nitrate- or iron/manganese-dependent AOM. However, we demonstrate for the first time that the methanotrophic archaea do not necessarily rely upon these oxidants as terminal electron acceptors directly, but mainly perform canonical sulfate-dependent AOM, which under sulfate-starved conditions can be supported by metal (Mn, Fe) oxides through oxidation of reduced sulfur species to sulfate. The correspondence of high abundances of Desulfobulbaceae andCandidatusMethanoperedens at the same sediment depth confirm the interdependence of anaerobic methane-oxidizing archaea and sulfate-reducing bacteria. The relatively high abundance and widespread distribution ofCandidatusMethanoperedens in lake sediments highlight their potentially important role in mitigating methane emissions from terrestrial freshwater environments to the atmosphere, analogous to ANME-1, -2 and -3 in marine settings.


2019 ◽  
Vol 65 (4) ◽  
pp. 863-875 ◽  
Author(s):  
Guangyi Su ◽  
Jakob Zopfi ◽  
Haoyi Yao ◽  
Lea Steinle ◽  
Helge Niemann ◽  
...  

2016 ◽  
Author(s):  
Matthias Egger ◽  
Peter Kraal ◽  
Tom Jilbert ◽  
Fatimah Sulu-Gambari ◽  
Célia J. Sapart ◽  
...  

Abstract. The surface sediments in the Black Sea are underlain by extensive deposits of iron (Fe) oxide-rich lake sediments that were deposited prior to the inflow of marine Mediterranean Sea waters ca. 9000 years ago. The subsequent downward diffusion of marine sulfate into the methane-bearing lake sediments has led to a multitude of diagenetic reactions in the sulfate-methane transition zone (SMTZ), including anaerobic oxidation of methane (AOM) with sulfate. While the sedimentary cycles of sulfur (S), methane and Fe in the SMTZ have been extensively studied, relatively little is known about the diagenetic alterations of the sediment record occurring below the SMTZ. Here we combine detailed geochemical analyses of the sediment and pore water with multicomponent diagenetic modeling to study the diagenetic alterations below the SMTZ at two sites in the western Black Sea. We focus on the dynamics of Fe, S and phosphorus (P) and demonstrate that diagenesis has strongly overprinted the sedimentary burial records of these elements. Our results show that sulfate-mediated AOM substantially enhances the downward diffusive flux of sulfide into the deep limnic deposits. During this downward sulfidization, Fe oxides, Fe carbonates and Fe phosphates (e.g. vivianite) are converted to sulfide phases, leading to an enrichment in solid phase S and the release of phosphate to the pore water. Below the sulfidization front, high concentrations of dissolved ferrous Fe (Fe2+) lead to sequestration of downward diffusing phosphate as authigenic vivianite, resulting in a transient accumulation of total P directly below the sulfidization front. Our model results further demonstrate that downward migrating sulfide becomes partly re-oxidized to sulfate due to reactions with oxidized Fe minerals, fueling a cryptic S cycle and thus stimulating slow rates of sulfate-driven AOM (~ 1–100 pmol cm−3 d−1) in the sulfate-depleted limnic deposits. However, this process is unlikely to explain the observed release of dissolved Fe2+ below the SMTZ. Instead, we suggest that besides organoclastic Fe oxide reduction, AOM coupled to the reduction of Fe oxides may also provide a possible mechanism for the high concentrations of Fe2+ in the pore water at depth. Our results reveal that methane plays a key role in the diagenetic alterations of Fe, S and P records in Black Sea sediments. The downward sulfidization into the limnic deposits is enhanced through sulfate-driven AOM with sulfate and AOM with Fe oxides may provide a deep source of dissolved Fe2+ that drives the sequestration of P in vivianite below the sulfidization front.


2018 ◽  
Vol 144 ◽  
pp. 332-340 ◽  
Author(s):  
Karla Martinez-Cruz ◽  
Armando Sepulveda-Jauregui ◽  
Peter Casper ◽  
Katey Walter Anthony ◽  
Kurt A. Smemo ◽  
...  

2020 ◽  
Author(s):  
Hanni Vigderovich ◽  
Werner Eckert ◽  
Orit Sivan

<p>Methane is a potent greenhouse gas that is produced naturally via microbial processes in anoxic environments (i.e. marine and lake sediments). The release of methane to the atmosphere from sediments is controlled by its aerobic and anaerobic oxidation. Anaerobic oxidation of methane (AOM) consumes up to 90% of the produced methane in marine sediments and over half of the produced methane in freshwater sediments. The most common electron acceptor in marine sediments for AOM is sulfate, however, in freshwater lake sediments, where sulfate concentrations are low, other electron acceptors can take its place (i.e. iron/manganese/nitrate). In lake Kinneret (Israel), iron-coupled AOM was evident by in-situ sedimentary profiles and in fresh sediment slurry incubations. Here we present geochemical and molecular analyses results of slurry experiments of long-term incubated lake Kinneret sediments with labeled <sup>13</sup>C-methane, different potential electron acceptors and a few inhibitors. These experiments are part of an ongoing research to characterize the AOM processes in lake sediments, and indicate another possible type of AOM that has evolved in the long-term incubated lake sediments.</p>


2016 ◽  
Vol 13 (18) ◽  
pp. 5333-5355 ◽  
Author(s):  
Matthias Egger ◽  
Peter Kraal ◽  
Tom Jilbert ◽  
Fatimah Sulu-Gambari ◽  
Célia J. Sapart ◽  
...  

Abstract. The surface sediments in the Black Sea are underlain by extensive deposits of iron (Fe)-oxide-rich lake sediments that were deposited prior to the inflow of marine Mediterranean Sea waters ca. 9000 years ago. The subsequent downward diffusion of marine sulfate into the methane-bearing lake sediments has led to a multitude of diagenetic reactions in the sulfate-methane transition zone (SMTZ), including anaerobic oxidation of methane (AOM) with sulfate. While the sedimentary cycles of sulfur (S), methane and Fe in the SMTZ have been extensively studied, relatively little is known about the diagenetic alterations of the sediment record occurring below the SMTZ.Here we combine detailed geochemical analyses of the sediment and porewater with multicomponent diagenetic modeling to study the diagenetic alterations below the SMTZ at two sites in the western Black Sea. We focus on the dynamics of Fe, S and phosphorus (P), and demonstrate that diagenesis has strongly overprinted the sedimentary burial records of these elements. In line with previous studies in the Black Sea, we show that sulfate-mediated AOM substantially enhances the downward diffusive flux of sulfide into the deep limnic deposits. During this downward sulfidization, Fe oxides, Fe carbonates and Fe phosphates (e.g., vivianite) are converted to sulfide phases, leading to an enrichment in solid-phase S and the release of phosphate to the porewater. Below the sulfidization front, high concentrations of dissolved ferrous Fe (Fe2+) lead to sequestration of downward-diffusing phosphate as authigenic vivianite, resulting in a transient accumulation of total P directly below the sulfidization front.Our model results further demonstrate that downward-migrating sulfide becomes partly re-oxidized to sulfate due to reactions with oxidized Fe minerals, fueling a cryptic S cycle and thus stimulating slow rates of sulfate-driven AOM ( ∼  1–100 pmol cm−3 d−1) in the sulfate-depleted limnic deposits. However, this process is unlikely to explain the observed release of dissolved Fe2+ below the SMTZ. Instead, we suggest that besides organoclastic Fe oxide reduction and reactivation of less reactive Fe oxides by methanogens, AOM coupled to the reduction of Fe oxides may also provide a possible mechanism for the high concentrations of Fe2+ in the porewater at depth. Our results reveal that methane plays a key role in the diagenetic alterations of Fe, S and P records in Black Sea sediments. The downward sulfidization into the limnic deposits is enhanced through sulfate-driven AOM with sulfate, and AOM with Fe oxides may provide a deep source of dissolved Fe2+ that drives the sequestration of P in vivianite below the sulfidization front.


2021 ◽  
Author(s):  
Antti J Rissanen ◽  
Tom Jilbert ◽  
Asko Simojoki ◽  
Rahul Mangayil ◽  
Sanni L Aalto ◽  
...  

ABSTRACTThe importance of nitrate in promoting anaerobic oxidation of methane (AOM) in the sediments of boreal lakes is currently unknown. Here we investigated the extent to which sediment AOM is linked to nitrate reduction in a nitrate-rich, oligo-mesotrophic, boreal lake (Lake Pääjärvi, Finland). AOM potential of sediment slurries, collected from three profundal stations of the study lake, was measured at varying nitrate concentrations using 13C-labelling. This was coupled with analysis of vertical profiles of the sediment and porewater geochemistry and the microbial communities (16S rRNA gene and shotgun metagenomic sequencing). Sediment AOM potential was enhanced by nitrate at a shallow station with high contents of labile phytoplankton-derived organic matter (Station 1), but not at the other two stations. AOM was also much higher at Station 1 (2.0-6.8 nmol C cm-3 d-1) than at the other stations (0-0.3 nmol C cm-3 d-1). Accordingly, methanotrophic archaea (Candidatus Methanoperedens sp.) and bacteria (Methylococcales) had the highest relative abundance at Station 1. Furthermore, geochemical profiles indicated that AOM was potentially coupled with reduction of nitrate, iron, or sulfate at all stations. We conclude that AOM linked to nitrate reduction takes place in boreal lake sediments. However, our data cannot resolve whether nitrate affects the process directly, via enhancing nitrate reduction-mediated AOM, or indirectly, via enhancing AOM mediated by reduction of other electron acceptors.One sentence summaryAnaerobic oxidation of methane linked to nitrate reduction in boreal lake sediments


2021 ◽  
Vol 194 ◽  
pp. 116928
Author(s):  
Wen-Bo Nie ◽  
Jie Ding ◽  
Guo-Jun Xie ◽  
Xin Tan ◽  
Yang Lu ◽  
...  

Solid Earth ◽  
2019 ◽  
Vol 10 (5) ◽  
pp. 1541-1554 ◽  
Author(s):  
Christian Stranne ◽  
Matt O'Regan ◽  
Martin Jakobsson ◽  
Volker Brüchert ◽  
Marcelo Ketzer

Abstract. Assessments of future climate-warming-induced seafloor methane (CH4) release rarely include anaerobic oxidation of methane (AOM) within the sediments. Considering that more than 90 % of the CH4 produced in ocean sediments today is consumed by AOM, this may result in substantial overestimations of future seafloor CH4 release. Here, we integrate a fully coupled AOM module with a numerical hydrate model to investigate under what conditions rapid release of CH4 can bypass AOM and result in significant fluxes to the ocean and atmosphere. We run a number of different model simulations for different permeabilities and maximum AOM rates. In all simulations, a future climate warming scenario is simulated by imposing a linear seafloor temperature increase of 3 ∘C over the first 100 years. The results presented in this study should be seen as a first step towards understanding AOM dynamics in relation to climate change and hydrate dissociation. Although the model is somewhat poorly constrained, our results indicate that vertical CH4 migration through hydraulic fractures can result in low AOM efficiencies. Fracture flow is the predicted mode of methane transport under warming-induced dissociation of hydrates on upper continental slopes. Therefore, in a future climate warming scenario, AOM might not significantly reduce methane release from marine sediments.


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