Spontaneously exsolved free gas during major storms as an ephemeral gas source for pockmark formation

Abrupt fluid emissions from shallow marine sediments pose a threat to seafloor installations like wind farms and offshore cables. Quantifying such fluid emissions and linking pockmarks, the seafloor manifestations of fluid escape, to flow in the sub-seafloor remains notoriously difficult due to an incomplete understanding of the underlying physical processes. Here, using a compositional multi-phase flow model, we test plausible gas sources for pockmarks in the south-eastern North Sea, which recent observations suggest have formed in response to major storms. We find that the mobilization of pre-existing gas pockets is unlikely because free gas, due to its high compressibility, damps the propagation of storm-induced pressure changes deeper into the subsurface. Rather, our results point to spontaneous appearance of a free gas phase via storm-induced gas exsolution from pore fluids. This mechanism is primarily driven by the pressure-sensitivity of gas solubility, and the appearance of free gas is largely confined to sediments in the vicinity of the seafloor. We show that in highly permeable sediments containing gas-rich pore fluids, wave-induced pressure changes result in the appearance of a persistent gas phase. This suggests that seafloor fluid escape structures are not always proxies for overpressured shallow gas and that periodic seafloor pressure changes can induce persistent free gas phase to spontaneously appear. Key Points - Storm-induced pressure changes can lead to spontaneous appearance of free gas phase near the seafloor - This process is driven by pressure-sensitive phase instabilities - This mechanism could help explain elusive gas sources in recently observed pockmarks in the North Se

Sedimentation-driven cyclic rebuilding of gas hydrates

Highlights • Sedimentation-driven gas hydrate recycling is cyclic in nature with time scales set by reactive multi-phase transport. • Each cycle can be divided into three distinct phases: 1) gas accumulation phase, 2) gas breakthrough phase and 3) uninhibited hydrate build-up phase. • In the presence of sufficient accumulated gas, convex deposition of hydrate acts like a mechanical nozzle for the ascending gas flow. Gas hydrate recycling is an important process in natural hydrate systems worldwide and frequently leads to the high gas hydrate saturations found close to the base of the gas hydrate stability zone (GHSZ). However, to date it remains enigmatic how, and under which conditions, free gas invades back into the GHSZ. Here we use a 1D compositional multi-phase flow model that accounts for sedimentation to investigate the dominant mechanisms that control free gas flow into the GHSZ using a wide-range of parameters i.e. hydrate formation kinetics, sediment permeability, and capillary pressure. In the first part of this study, we investigate free gas invasion into the GHSZ without any sedimentation, and analyse the dynamics of hydrate formation in the vicinity of the base of GHSZ. This helps establish plausible initial conditions for the main part of the study, namely, hydrate recycling due to rapid and continuous sedimentation. For the case study, we apply our numerical model to the Green Canyon Site 955 in the Gulf of Mexico, where the reported high hydrate saturations are likely a result of hydrate recycling driven by rapid sedimentation. In the model, an initial hydrate layer forms due to the invasion of a specified volume of rising free gas. This hydrate layer is consistent with the local pressure, temperature and salinity state. This hydrate layer is then thermally de-stabilised by sedimentation resulting in free gas formation and hydrate recycling. A key finding of our study is that gas hydrate recycling is a cyclic process which can be divided into three phases of 1) gas hydrate melting and free gas nozzling through the hydrate layer, 2) formation of a new gas hydrate layer as the old layer vanishes, and 3) fast uninhibited grow of a new hydrate layer. High hydrate saturations of about 80% can be attained purely through physical, burial-driven recycling of gas hydrates, without any additional gas input from other sources. Hydrate recycling is, therefore, highly dynamic with its own inherent cyclicity rather than a gradual process paced by the rate of sediment deposition