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In the past 20 years, the exploration of deep ocean trenches has led to spectacular new insights. Even in the deepest canyons, an unusual variety of life and unexpectedly high benthic oxygen consumption rates have been detected while microbial processes below the surface of the hadal seafloor remains largely unknown. The information that exist comes from geophysical measurements, especially related to seismic research, and specific component analyses to estimate the carbon export. In contrast, no information is available on metabolic activities in deeper buried sediments of hadal environment. Here we present the first pore water profiles from 15 up to 11 m long sediment cores recovered during three expeditions to two hadal zones, the Japan Trench and the Atacama Trench. Despite low levels of organic debris, our data reveal that rates of microbial carbon turnover along the trench axes can be similar to those encountered in much shallower and more productive oceanic regions. The extreme sedimentation dynamics, characterized by frequent mass wasting of slope sediments into the trenches, result in effective burial of reactive, microbially available, organic material. Our results document the fueling of the deep hadal biosphere with bioavailable material and thus provide important understanding on the function of deep‐sea trenches and the hadal carbon cycle. Plain Language Summary: For a long time, it was assumed that in water depths below 6,000 m, biological species diversity and microbial activity is very low. Recent studies could already provide clear evidence that significant degradation of organic material occurs even at the seafloor surface in deep‐sea trenches. No comparable information is available yet about the situation below the surface layer. Here, data are presented for the first time that help to close this knowledge gap. Based on geochemical parameters, it can be proven that very active degradation processes also take place in the deeper buried layers in deep‐sea trenches. Rates correspond in magnitude to sediments from shallower water depths with considerably higher contents of organic material. The authors attribute this finding primarily to sedimentation dynamics in deep‐sea trenches. The steep flanks of trenches, sometimes associated with seismic activity, repeatedly favor the sliding of large sediment packages into basins along trench axes. Rapid burial removes less degraded, and thus more microbially available material from oxic surface and preserves it for subsequent processes such as sulfate reduction. The unique results provide important new insights into the function of deep‐sea trenches and the hadal carbon cycle. Key Points: Hadal subseafloor pore water profiles from the Japan Trench and Atacama Trench document unexpectedly high microbial turnover ratesFrequent alternations between hemipelagic sedimentation and mass wasting lead to high burial efficiency of reactive organic carbonMicrobial activities in deep‐sea trenches may be similar to those at the edge of high‐production areas [ABSTRACT FROM AUTHOR]

Anaerobic methane-oxidizing microbial communities in sediments at cold methane seeps are important factors in controlling methane emission to the ocean and atmosphere. Here, we investigated the distribution and carbon isotopic signature of specific biomarkers derived from anaerobic methanotrophic archaea (ANME groups) and sulphate-reducing bacteria (SRB) responsible for the anaerobic oxidation of methane (AOM) at different cold seep provinces of Hydrate Ridge, Cascadia margin. The special focus was on their relation to in situ cell abundances and methane turnover. In general, maxima in biomarker abundances and minima in carbon isotope signatures correlated with maxima in AOM and sulphate reduction as well as with consortium biomass. We found ANME-2a/DSS aggregates associated with high abundances of sn-2,3-di- O-isoprenoidal glycerol ethers (archaeol, sn-2-hydroxyarchaeol) and specific bacterial fatty acids (C16:1ω5c, cyC17:0ω5,6) as well as with high methane fluxes ( Beggiatoa site). The low to medium flux site ( Calyptogena field) was dominated by ANME-2c/DSS aggregates and contained less of both compound classes but more of AOM-related glycerol dialkyl glycerol tetraethers (GDGTs). ANME-1 archaea dominated deeper sediment horizons at the Calyptogena field where sn-1,2-di- O-alkyl glycerol ethers (DAGEs), archaeol, methyl-branched fatty acids ( ai-C15:0, i-C16:0, ai-C17:0), and diagnostic GDGTs were prevailing. AOM-specific bacterial and archaeal biomarkers in these sediment strata generally revealed very similar δ13C-values of around −100. In ANME-2-dominated sediment sections, archaeal biomarkers were even more 13C-depleted (down to −120), whereas bacterial biomarkers were found to be likewise 13C-depleted as in ANME-1-dominated sediment layers (δ13C: −100). The zero flux site ( Acharax field), containing only a few numbers of ANME-2/DSS aggregates, however, provided no specific biomarker pattern. Deeper sediment sections (below 20 cm sediment depth) from Beggiatoa covered areas which included solid layers of methane gas hydrates contained ANME-2/DSS typical biomarkers showing subsurface peaks combined with negative shifts in carbon isotopic compositions. The maxima were detected just above the hydrate layers, indicating that methane stored in the hydrates may be available for the microbial community. The observed variations in biomarker abundances and 13C-depletions are indicative of multiple environmental and physiological factors selecting for different AOM consortia (ANME-2a/DSS, ANME-2c/DSS, ANME-1) along horizontal and vertical gradients of cold seep settings. [ABSTRACT FROM AUTHOR]

The article discusses a study on methane emission and consumption at a gas seepage in the North Sea. It provides an overview of the materials and methodologies used in the study. It also includes information on equations used to calculate sulphate reduction rates. The results of the study are analyzed.

This study describes the microbial community structure of three sandy sediment stations that differed with respect to median grain size and permeability in the German Bight of the Southern North Sea. The microbial community was investigated using lipid biomarker analyses and fluorescencein situhybridization. For further characterization we determined the stable carbon isotope composition of the biomarkers. Biomarkers identified belong to different bacterial groups such as members of theCytophaga-Flavobacteriumcluster and sulfate-reducing bacteria (SRB). To support these findings, investigations using different fluorescent in situ hybridization probes were performed, specifically targetingCytophaga-Flavobacterium,γ-Proteobacteria and different members of the SRB. Depth profiles of bacterial fatty acid relative abundances revealed elevated subsurface peaks for the fine sediment, whereas at the other sandy sediment stations the concentrations were less variable with depth. Although oxygen penetrates deeper into the coarser and more permeable sediments, the SRB biomarkers are similarly abundant, indicating suboxic to anoxic niches in these environments. We detected SRB in all sediment types as well as in the surface and at greater depth, which suggests that SRB play a more important role in oxygenated marine sediments than previously thought. [ABSTRACT FROM AUTHOR]

Serpentinite-hosting mud volcanoes, located in the Marianna forearc subduction zone, were drilled during IODP Expedition 366. Recovered samples from Asùt Tesoru seamount provide new insights on the generation of organic matter in deep environments. Short-chain alcohols, volatile fatty acids and light hydrocarbons are produced within hyperalkaline pore fluids (pH 12.5) rich in H2. The stable isotope values of those species show heavy δ13C values, suggesting a formation process through Fischer-Tropsch-Type reactions. This close isotopic study brings new constraints on the reaction pathways leading to the formation of not only light hydrocarbons, but also of short-chain organic molecules. These compounds may serve as precursors of building blocks essential to life in deep oceanic settings.

Microbial life inhabits deeply buried marine sediments, but the extent of this vast ecosystem remains poorly constrained. Here we provide evidence for the existence of microbial communities in ~40° to 60°C sediment associated with lignite coal beds at ~1.5 to 2.5 km below the seafloor in the Pacific Ocean off Japan. Microbial methanogenesis was indicated by the isotopic compositions of methane and carbon dioxide, biomarkers, cultivation data, and gas compositions. Concentrations of indigenous microbial cells below 1.5 km ranged from <10 to ~104 cells cm-3. Peak concentrations occurred in lignite layers, where communities differed markedly from shallower subseafloor communities and instead resembled organotrophic communities in forest soils. This suggests that terrigenous sediments retain indigenous community members tens of millions of years after burial in the seabed. [ABSTRACT FROM AUTHOR]