Description: Highlights • Mega ebullition of biogenic methane from an abandoned offshore gas well, North Sea. • Evidence for midwater bubble plume intrusion, fallback, and short-circuiting of the plume. • Effective trapping of seabed released methane underneath the thermocline. • First observation of a spiral vortex methane plume and marginal turbulences. • Megaplumes appear less efficient in terms of vertical methane transport than previously thought. Abstract First direct evidence for ongoing gas seepage activity on the abandoned well site 22/4b (Northern North Sea, 57°55′ N, 01°38′ E) and discovery of neighboring seepage activity is provided from observations since 2005. A manned submersible dive in 2006 discovered several extraordinary intense seepage sites within a 60 m wide and 20 m deep crater cut into the flat 96 m deep seafloor. Capture and (isotope) chemical analyses of the gas bubbles near the seafloor revealed in situ concentrations of methane between 88 and 90%Vol. with δ13C–CH4 values around −74‰ VPDB, indicating a biogenic origin. Bulk methane concentrations throughout the water column were assessed by 120 Niskin water samples showing up to 400.000 nM CH4 in the crater at depth. In contrast, concentrations above the thermocline were orders of magnitude lower, with a median value of 20 nM. A dye tracer injection into the gas seeps revealed upwelling bubble and water motion with gas plume rise velocities up to ∼1 ms−1 (determined near the seabed). However, the dissolved dye did not pass the thermocline, but returned down to the seabed. Measurements of direct bubble-mediated atmospheric flux revealed low values of 0.7 ± 0.3 kty−1, much less than current state-of-the-art bubble dissolution models would predict for such a strong and upwelling in situ gas bubble flux at shallow water depths (i.e. ∼100 m). Acoustic multibeam water column imaging data indicate a pronounced 200 m lateral intrusion at the thermocline together with high methane concentration at this layer. A partly downward-orientated bubble plume motion is also visible in the acoustic data with potential short-circuiting in accordance to the dye experiment. This observation could partly explain the observed trapping of most of the released gas below the well-established thermocline in the North Sea. Moreover, 3D analyses of the multibeam water column data reveal that the upwelling plume transforms into a spiral expanding vortex while rising through the water column. Such a spiral vortex motion has never been reported before for marine gas seepage and might represent an important process with strong implication on plume dynamics, dissolution behavior, gas escape to the atmosphere, and is considered very important for respective modeling approaches.

Description: Extremely intense bubble plumes, like the North Sea 22/4b blowout megaplume (defined as more than 10(6) L day(-1)), create very strong upwelling flows (〉1 m s(-1)), which lead to detrainment of methane-enriched water, but leave direct bubble-mediated transport unaffected. Dissolved CH4 depth profiles and atmospheric measurements during a fall 2011 survey of the 22/4b site suggest strong constraint of seabed CH4 below the thermocline. Seabed bubbles were nearly pure CH4. The effect of the upwelling flow on the fate of bubble plume CH4 was investigated with a numerical bubble-propagation model. The model considered different representative bubble plume size distributions, phi, and a global (total) megaplume bubble size distribution, Phi, synthesized from video survey data and phi from the literature. Simulations showed that none of the literature plumes or variations in the upwelling flow could constrain CH4 sufficiently below the thermocline. Two new bubble megaplume processes were simulated, vortical bubble trapping (slow rise) and a hypothesized, enhanced bubble gas exchange, k(BE), an enhancement factor applied to the normal bubble gas exchange rate, k(B). The latter could arise from plume turbulence increasing bubble boundary-layer turbulence and thus its gas exchange. Observations could not be reproduced solely by slow rise, however, simulations with k(BE)similar to 6 reproduced observational constraints, as could weaker k(BE) in conjunction with slow rise. Field validation of k(BE) is needed given its implications for the fate of megaplume CH4 emissions (anthropogenic or natural) for stratified and unstratified conditions. kBE suggests marine CH4 geologic contributions to the atmosphere from all but shallow waters primarily arises from bubble plumes that are less than megaplume size.

Description: The scientific community is engaged in a lively debate over whether and how venting from the gas-hydrate reservoir and the Earth’s climate is connected. The various scenarios which have been proposed are based on the following assumptions: the inventory of methane gas-hydrate deposits is locally enormous, the stability of marine gas-hydrate deposits can easily be perturbed by temperature and pressure changes, enough methane can be released from these deposits to contribute adequate volumes of this isotopically distinct greenhouse gas to alter the composition of oceanic or atmospheric methane reservoirs, and the mechanisms exist for the transfer of methane from deeper geologic reservoirs to the ocean and/or atmosphere. However, some potential transfer mechanisms have been difficult to evaluate. Here, we consider the possibility of marine slumping as a mechanism to transfer methane carbon from gas hydrates within the seafloor into the ocean and atmosphere. Our analyses and field experiments indicate that large slumps could release volumetrically significant quantities of solid gas hydrates which would float upwards in the water column. Large pieces of gas hydrate would reach the upper layers of the ocean before decomposing, and some of the methane would be directly injected into the atmosphere.

Description: To help constrain models involving the chemical stability and lifetime of gas clathrate hydrates exposed at the seafloor, dissolution rates of pure methane and carbon-dioxide hydrates were measured directly on the seafloor within the nominal pressure-temperature (P/T) range of the gas hydrate stability zone. Other natural boundary conditions included variable flow velocity and undersaturation of seawater with respect to the hydrate-forming species. Four cylindrical test specimens of pure, polycrystalline CH4 and CO2 hydrate were grown and fully compacted in the laboratory, then transferred by pressure vessel to the seafloor (1028 m depth), exposed to the deep ocean environment, and monitored for 27 hours using time-lapse and HDTV cameras. Video analysis showed diameter reductions at rates between 0.94 and 1.20 μm/s and between 9.0 and 10.6 · 10−2 μm/s for the CO2 and CH4 hydrates, respectively, corresponding to dissolution rates of 4.15 ± 0.5 mmol CO2/m2s and 0.37 ± 0.03 mmol CH4/m2s. The ratio of the dissolution rates fits a diffusive boundary layer model that incorporates relative gas solubilities appropriate to the field site, which implies that the kinetics of the dissolution of both hydrates is diffusion-controlled. The observed dissolution of several mm (CH4) or tens of mm (CO2) of hydrate from the sample surfaces per day has major implications for estimating the longevity of natural gas hydrate outcrops as well as for the possible roles of CO2 hydrates in marine carbon sequestration strategies.

Description: The methane concentration and pCO2 in surface waters and the overlying marine air were continuously surveyed along the pathway of the Kuroshio, from the eastern coast of Honshu to Taiwan, and then across the eastern part of the East China and South China Seas in September of 1994. Off Honshu, the CH4 content was controlled by the confluence of the relatively CH4-poor waters of the Kuroshio and the Oyashio and the CH4-rich Tsugaru Warm Current, the latter carrying water into the Pacific Ocean with a methane content more than twice the equilibrium value with the atmospheric CH4 partial pressure. Along the Kuroshio, the surface water was supersaturated in methane with respect to the atmosphere by 10–15% and appears considerably enriched relative to open Pacific surface waters at same latitudes. The northeastern part of the South China Sea, part of the deep basin of this marginal sea, showed CH4 concentrations similar to those found in open-ocean waters. In contrast, highly variable oversaturations up to 700% were observed along the northwestern coast of Borneo, most probably related to known seepage from oil and gas deposits in this area. The pCO2 of surface water was higher than the atmospheric pCO2 throughout the area surveyed. However, the ΔpCO2 of the surface waters varied from close to 0 to more than 60 μatm. The observed oversaturation in areas influenced by the Kuroshio confirm that, during a short period in late summer, the surface waters of this current between Taiwan and Japan act as a moderate source for atmospheric CO2.

Description: A pockmark field was discovered during EM-300 multi-beam bathymetric surveys on the lower continental slope off the Big Sur coast of California. The field contains ∼1500 pockmarks which are between 130 and 260 m in diameter, and typically are 8–12 m deep located within a 560 km2 area. To investigate the origin of these features, piston cores were collected from both the interior and the flanks of the pockmarks, and remotely operated vehicle observation (ROV) video and sampling transects were conducted which passed through 19 of the pockmarks. The water column within and above the pockmarks was sampled for methane concentration. Piston cores and ROV collected push cores show that the pockmark field is composed of monotonous fine silts and clays and the cores within the pockmarks are indistinguishable from those outside the pockmarks. No evidence for either sediment winnowing or diagenetic alteration suggestive of fluid venting was obtained. 14C measurements of the organic carbon in the sediments indicate continuous sedimentation throughout the time resolution of the radiocarbon technique (∼45 000 yr BP), with a sedimentation rate of ∼10 cm per 1000 yr both within and between the pockmarks. Concentrations of methane, dissolved inorganic carbon, sulfate, chloride, and ammonium in pore water extracted from within the cores are generally similar in composition to seawater and show little change with depth, suggesting low biogeochemical activity. These pore water chemical gradients indicate that neither significant accumulations of gas are likely to exist in the shallow subsurface (∼100 m) nor is active fluid advection occurring within the sampled sediments. Taken together the data indicate that these pockmarks are more than 45 000 yr old, are presently inactive, and contain no indications of earlier fluid or gas venting events.