Description: In the Arctic Seas, the West Spitsbergen continental margin represents a prominent methane seep area. In this area, free gas formation and gas ebullition as a consequence of hydrate dissociation due to global warming are currently under debate. Recent studies revealed shallow gas accumulation and ebullition of methane into the water column at more than 250 sites in an area of 665 km2. We conducted a detailed study of a subregion of this area, which covers an active gas ebullition area of 175 km2 characterized by 10 gas flares reaching from the seafloor at~245 m up to 50 m water depth to identify the fate of the released gas due to dissolution of methane from gas bubbles and subsequent mixing, transport and microbial oxidation. The oceanographic data indicated a salinity-controlled pycnocline situated ~20 m above the seafloor. A high resolution sampling program at the pycnocline at the active gas ebullition flare area revealed that the methane concentration gradient is strongly controlled by the pycnocline. While high methane concentrations of up to 524 nmol L−1 were measured below the pycnocline, low methane concentrations of less than 20 nmol L−1 were observed in the water column above. Variations in the δ13CCH4 values point to a 13C depleted methane source (~−60‰ VPDB) being mainly mixed with a background values of the ambient water (~−37.5‰ VPDB). A gas bubble dissolution model indicates that ~80% of the methane released from gas bubbles into the ambient water takes place below the pycnocline. This dissolved methane will be laterally transported with the current northwards and most likely microbially oxidized in between 50 and 100 days, since microbial CH4 oxidation rates of 0.78 nmol d−1 were measured. Above the pycnocline, methane concentrations decrease to local background concentration of ~10 nmol L−1. Our results suggest that the methane dissolved from gas bubbles is efficiently trapped below the pycnocline and thus limits the methane concentration in surface water and the air–sea exchange during summer stratification. During winter the lateral stratification breaks down and fractions of the bottom water enriched in methane may be vertically mixed and thus be potentially an additional source for atmospheric methane.

Description: Tommeliten is a prominent methane seep area in the Central North Sea. Previous surveys revealed shallow gas-bearing sediments and methane gas ebullition into the water column. In this study, the in situ methane flux at Tommeliten is re-assessed and the potential methane transport to the atmosphere is discussed, with regards to the hydrographic setting and gas bubble modeling. We have compiled previous data, acquired new video and acoustic evidence of gas bubble release, and have measured the methane concentration, and its C-isotopic composition in the water column. Parametric subbottom sonar data reveal the three-dimensional extent of shallow gas and morphologic features relevant for gas migration. Five methane ebullition areas are identified and the main seepage area appears to be 21 times larger than previously estimated. Our video, hydroacoustic, subbottom, and chemical data suggest that 1.5106 mol CH4/yr (26 tons CH4/yr) of methane gas is being released from the seepage area of Tommeliten. Methane concentration profiles in the vicinity of the gas seeps show values of up to 268 nM (100 times background) close to the seafloor. A decrease in d13C-CH4 values at 40 m water depth indicates an unknown additional biogenic methane source within the well oxygenated thermocline between 30 and 40 m water depth. Numerical modeling of the methane bubbles due to their migration and dissolution was performed to estimate the bubble-derived vertical methane transport, the fate of this methane in the water column, and finally the flux to the atmosphere. Modeling indicates that less than 4% of the gas initially released at the seafloor is transported via bubbles into the mixed layer and, ultimately, to the atmosphere. However, because of the strong seasonality of mixing in the North Sea, this flux is expected to increase as mixing increases, and almost all of the methane released at the seafloor could be transferred into the atmosphere in the stormy fall and winter time.

Description: In situ methane emission measurements from sediments are combined with water column backscatter anomalies recorded with an Acoustic Doppler Current Profiler (ADCP) integrated on a benthic observatory. During cruise SO191 to the Hikurangi Margin (New Zealand), the Fluid Flux Observatory (FLUFO) was deployed at a cold seep site at Omakere Ridge. The sediments incubated in the two benthic chambers of FLUFO contained seep-associated fauna, including small and larger tubeworms, juvenile bivalves of the genus Acharax and some juvenile clams. The first 26 h of in situ incubation revealed low to moderate methane fluxes of 0.01 to 0.4 mmol m− 2 d− 1 into the overlying water of the backup and flux chamber, respectively. In the following sampling sequence, however, the methane concentration in the flux chamber reached 3-fold higher concentrations whereas the methane concentration in the backup chamber remained low and unchanged. Simultaneous to the sudden methane increase, a significant backscatter anomaly was recorded and persisted for 30 min and covered the entire depth range (100 m) of the upward looking ADCP. Data analyses revealed that a single-phase plume (no bubbles) outburst likely occurred during this time. While bubbles appeared to be present during some periods, plume simulations revealed that the volume of gas required (rate of 8 ton/day) does not support a bubble plume. A second data set was obtained during lander deployments at Rock Garden where visual observations by ROV confirmed the transient pattern of free gas injection into the water column. Acoustic flares and methane concentration increase in the bottom water hint towards a pressure (tidal) induced discharge mechanism. The presented data demonstrate the temporal and spatial variability of seabed methane emission, and very short methane signal lifetime in the water column (hours to a few days) due to turbulent diffusion. Both have to be considered when methane budgets are extrapolated from single methane emission rates.

Description: As a result of extensive hydrocarbon exploration, the North Sea hosts several thousand abandoned wells; many believed to be leaking methane. However, how much of this greenhouse gas is emitted into the water column and ultimately reaches the atmosphere is not known. Here, we investigate three abandoned wells at 81-93m water depth in the Norwegian sector of the North Sea, all of which show gas seepage into the bottom water. The isotopic signature of the emanating gas points towards a biogenic origin and hence to gas pockets in the sedimentary overburden above the gas reservoirs that the wells were drilled into. Video-analysis of the seeping gas bubbles and direct gas flow measurements resolved initial bubble sizes ranging between 3.2 and 7.4mm in diameter with a total seabed gas flow between 1 and 19 tons of CH4 per year per well. Estimated total annual seabed emissions from all three wells of ~24 tons are similar to the natural seepage rates at Tommeliten, suggesting that leaky abandoned wells represent a significant source of methane into North Sea bottom waters. However, the bubble-driven direct methane transport into the atmosphere was found to be negligible (〈2%) due to the small bubble sizes and the water depth at which they are released.

Description: The concentration and carbon isotope values of dissolved methane were measured in the water column at Rock Garden, Omakere Ridge and Wairarapa areas in the first dedicated cold seep investigation along the Hikurangi Margin of New Zealand. These measurements provide a high resolution impression of the methane distribution in the water column and show that these seep sites are actively venting methane with varying intensity. The highest concentrations (up to 3500 nM) measured in water samples obtained from Conductivity–Temperature–Depth (CTD) operations were at Faure Site of Rock Garden. Here, seafloor bubble release was observed by ROV. The Omakere Ridge area is actively venting over almost its entire length (not, vert, similar 25 km), in particular at Bear's Paw, a newly discovered seep site. In the Wairarapa area another new seep site called Tui was discovered, where methane measurements often exceeded 500 nM. No evidence was obtained from water column or sea surface measurements along the Hikurangi Margin to indicate that methane from seeps is reaching the sea surface. In fact, a consistent upper boundary was observed at a density of 26.85 kg/m3, which occurs at about 500 m below sea surface, above which methane decreased to background concentrations. No obvious oceanographic feature is associated with this 500 m CH4 boundary. Bubble dissolution calculations show that about 500 m was also the model-derived maximum bubble rise height. A wide range of δ13CCH4 values from − 71 to − 19‰ (VPDB) were measured, with the highest CH4 concentrations having the lowest δ13CCH4 values of about − 71 to − 68‰. Simple mixing and isotope fractionation calculations show that changes of δ13CCH4 values are predominantly caused by the dilution of seep fluids with the seawater, with some anaerobic oxidation also occurring.

Description: The presented software application allows GUI-based access to the bubble dissolution model presented by McGinnis et al. [McGinnis, D.F., Greinert, J., Artemov, Y., Beaubien, S.E., Wüest, A., 2006. The fate of rising methane bubbles in stratified waters: what fraction reaches the atmosphere? Journal of Geophysical Research 111, C09007. doi:http://dx.doi.org/10.1029/2005JC003183]. It quantifies the dissolution of gas bubbles (containing any combination of CH4, CO2, O2, N2, and Ar) in marine or lacustrine environments based on the initial bubble size, free gas composition and environmental parameters (temperature, salinity, and dissolved gas concentrations). The software enables scientists and engineers to evaluate bubble dynamics in a simple way on Windows® PCs