Description: Large quantities of the greenhouse gas methane (CH4) are stored in the seafloor. The flux of CH4 from the sediments into the water column and finally to the atmosphere is mitigated by a series of microbial methanotrophic filter systems of unknown efficiency at highly active CH4-release sites in shallow marine settings. Here, we studied CH4-oxidation and the methanotrophic community at a high-CH4-flux site in the northern North Sea (well 22/4b), where CH4 is continuously released since a blowout in 1990. Vigorous bubble emanation from the seafloor and strongly elevated CH4 concentrations in the water column (up to 42 µM) indicated that a substantial fraction of CH4 bypassed the highly active (up to ∼2920 nmol cm−3 d−1) zone of anaerobic CH4-oxidation in sediments. In the water column, we measured rates of aerobic CH4-oxidation (up to 498 nM d−1) that were among the highest ever measured in a marine environment and, under stratified conditions, have the potential to remove a significant part of the uprising CH4 prior to evasion to the atmosphere. An unusual dominance of the water-column methanotrophs by Type II methane-oxidizing bacteria (MOB) is partially supported by recruitment of sedimentary MOB, which are entrained together with sediment particles in the CH4 bubble plume. Our study thus provides evidence that bubble emission can be an important vector for the transport of sediment-borne microbial inocula, aiding in the rapid colonization of the water column by methanotrophic communities and promoting their persistence close to highly active CH4 point sources.

Description: Gas migration pathways in the Gulf of Mexico are strongly influenced by the extensive formation and time evolution of salt canopies, welds and sheets. This multi-level salt system (known as the Louann Salt formation) deposited mostly within Callovian age (upper Middle Jurassic) and mobilized during late Miocene up to Pliocene-Pleistocene times controls the extension and direction of petroleum components migration over the entire history of the basin which, in return, has a major impact on potential gas transportation into the gas hydrate stability zone (GHSZ). In the context of gas hydrate formation, presence of extensive salt deposits tends to bend gas migration pathways from vertical (typical for the Gulf of Mexico region) towards rather horizontal and dispersed. However, amalgamation of two or more salt structures often results in re-focusing of the flow towards the local topographic subsalt heights. Together with the formation of local sediment discontinuity structures such as faults developing at the rims and tops of rootless salt deposits related to further stages of allochthonous salt mobilization, new high-permeability migration pathways develop and act as direct connection for the thermogenic gas to the GHSZ. Our study presents the 3D modeling solution quantifying and exploring the gas hydrate accumulation potential in the marine environment experiencing salt tectonics such as the Green Canyon, Gulf of Mexico. This modeling study evaluates the potential of bio- and thermogenic gas hydrate formation within Pliocene-Pleistocene reservoir layers based on full basin re-construction which accounts for depositional and transient thermal history of the basin, source rock maturation, petroleum generation, expulsion and migration, salt tectonics and associated faults development. Based on a numerical study calibrated with the existing field data, we present a new distribution pattern of gas hydrates attributed to both microbial and thermogenic origin. We present here an explanation for a formation mechanism of large gas hydrate amounts (〉 70 vol. %) wide-spread at the base of the stability zone as a result of the gas hydrate-free gas recycling process enhanced by very high Neogene sedimentation rates in the region. We suggest that the rapid development of secondary intra-salt mini-basins situated on top of the allochthonous salt deposits and following sediment subsidence caused a consequent dislocation of the GHSZ lower boundary and led to efficient gas hydrate dissociation process followed by a free gas re-charge into the GHSZ.

Description: Highlights • Polypropylene and biodegradable plastic bags were incubated in marine sediments. • Bacterial colonization was highest on biodegradable plastic bags. • None of the two bag types showed signs of degradation after 98 days. • Marine sediments probably represent a long-term sink for both types of litter. Abstract To date, the longevity of plastic litter at the sea floor is poorly constrained. The present study compares colonization and biodegradation of plastic bags by aerobic and anaerobic benthic microbes in temperate fine-grained organic-rich marine sediments. Samples of polyethylene and biodegradable plastic carrier bags were incubated in natural oxic and anoxic sediments from Eckernförde Bay (Western Baltic Sea) for 98 days. Analyses included (1) microbial colonization rates on the bags, (2) examination of the surface structure, wettability, and chemistry, and (3) mass loss of the samples during incubation. On average, biodegradable plastic bags were colonized five times higher by aerobic and eight times higher by anaerobic microbes than polyethylene bags. Both types of bags showed no sign of biodegradation during this study. Therefore, marine sediment in temperate coastal zones may represent a long-term sink for plastic litter and also supposedly compostable material.

Description: Large quantities of methane are stored in hydrates and permafrost within shallow marine sediments in the Arctic Ocean. These reservoirs are highly sensitive to climate warming, but the fate of methane released from sediments is uncertain. Here, we review the principal physical and biogeochemical processes that regulate methane fluxes across the seabed, the fate of this methane in the water column, and potential for its release to the atmosphere. We find that, at present, fluxes of dissolved methane are significantly moderated by anaerobic and aerobic oxidation of methane. If methane fluxes increase then a greater proportion of methane will be transported by advection or in the gas phase, which reduces the efficiency of the methanotrophic sink. Higher freshwater discharge to Arctic shelf seas may increase stratification and inhibit transfer of methane gas to surface waters, although there is some evidence that increased stratification may lead to warming of sub-pycnocline waters, increasing the potential for hydrate dissociation. Loss of sea-ice is likely to increase wind speeds and seaair exchange of methane will consequently increase. Studies of the distribution and cycling of methane beneath and within sea ice are limited, but it seems likely that the sea-air methane flux is higher during melting in seasonally ice-covered regions. Our review reveals that increased observations around especially the anaerobic and aerobic oxidation of methane, bubble transport, and the effects of ice cover, are required to fully understand the linkages and feedback pathways between climate warming and release of methane from marine sediments.

Description: This study presents 2D seismic reflection data, seismic velocity analysis, as well as geochemical and isotopic porewater compositions from Opouawe Bank on New Zealand’s Hikurangi subduction margin, providing evidence for essentially pure methane gas seepage. The combination of geochemical information and seismic reflection images is an effective way to investigate the nature of gas migration beneath the seafloor, and to distinguish between water advection and gas ascent. The maximum source depth of the methane that migrates to the seep sites on Opouawe Bank is 1,500–2,100 m below seafloor, generated by low-temperature degradation of organic matter via microbial CO2 reduction. Seismic velocity analysis enabled identifying a zone of gas accumulation underneath the base of gas hydrate stability (BGHS) below the bank. Besides structurally controlled gas migration along conduits, gas migration also takes place along dipping strata across the BGHS. Gas migration on Opouawe Bank is influenced by anticlinal focusing and by several focusing levels within the gas hydrate stability zone.

Description: Highlights • PetroMod is the 1st basin modelling software including methane hydrate simulation. • The Gas hydrate module includes physical, thermodynamic, and kinetic properties. • PetroMod simulates the evolution over time of the GHSZ. • PetroMod includes a kinetic for the organic matter degradation at low temperature. Abstract Within the German gas hydrate initiative SUGAR, a new 2-D/3-D module simulating the biogenic generation of methane from organic matter and the formation of gas hydrates has been developed and included in the petroleum systems modelling software package PetroMod®. Typically, PetroMod® simulates the thermogenic generation of multiple hydrocarbon components (oil and gas), their migration through geological strata, finally predicting oil and gas accumulations in suitable reservoir formations. We have extended PetroMod® to simulate gas hydrate accumulations in marine and permafrost environments by the implementation of algorithms describing (1) the physical, thermodynamic, and kinetic properties of gas hydrates; and (2) a kinetic continuum model for the microbially mediated, low temperature degradation of particulate organic carbon in sediments. Additionally, the temporal and spatial resolutions of PetroMod® were increased in order to simulate processes on time scales of hundreds of years and within decimetres of spatial extension. In order to validate the abilities of the new hydrate module, we present here results of a theoretical layer-cake model. The simulation runs predict the spatial distribution and evolution in time of the gas hydrate stability field, the generation and migration of thermogenic and biogenic methane gas, and its accumulation as gas hydrates.

Description: Takahe seep, located on the Opouawe Bank, Hikurangi Margin, is characterized by a well-defined subsurface seismic chimney structure ca. 80,500 m2 in area. Sub-seafloor geophysical data based on acoustic anomaly layers indicated the presence of gas hydrate and free gas layers within the chimney structure. Reaction-transport modeling was applied to porewater data from 11 gravity cores to constrain methane turnover rates and benthic methane fluxes in the upper 10 m. Model results show that methane dynamics were highly variable due to transport and dissolution of ascending gas. The dissolution of gas (up to 3761 mmol m−2 yr−1) dwarfed the rate of methanogenesis within the simulated sediment column (2.6 mmol m−2 yr−1). Dissolved methane is mainly consumed by anaerobic oxidation of methane (AOM) at the base of the sulfate reduction zone and trapped by methane hydrate formation below it, with maximum rates in the central part of the chimney (946 and 2420 mmol m−2 yr−1, respectively). A seep-wide methane budget was constrained by combining the biogeochemical model results with geophysical data and led to estimates of AOM rates, gas hydrate formation and benthic dissolved methane fluxes of 3.68 × 104 mol yr−1, 73.85 × 104 mol yr−1and 1.19 × 104 mol yr−1, respectively. A much larger flux of methane probably escapes in gaseous form through focused bubble vents. The approach of linking geochemical model results with spatial geophysical data put forward here can be applied elsewhere to improve benthic methane turnover rates from limited single spot measurements to larger spatial scales.