Destabilization of intrapermafrost gas hydrates is one of the possible mechanisms responsible for methane emission in the Arctic shelf. Intrapermafrost gas hydrates may be coeval to permafrost: they originated during regression and subsequent cooling and freezing of sediments, which created favorable conditions for hydrate stability. Local pressure increase in freezing gas-saturated sediments maintained gas hydrate stability from depths of 200–250 meters or shallower. The gas hydrates that formed within shallow permafrost have survived till present in the metastable (relict) state. The metastable gas hydrates located above the present stability zone may dissociate in the case of permafrost degradation as it becomes warmer and more saline. The effect of temperature increase on frozen sand and silt containing metastable pore methane hydrate is studied experimentally to reconstruct the conditions for intrapermafrost gas hydrate dissociation. The experiments show that the dissociation process in hydrate-bearing frozen sediments exposed to warming begins and ends before the onset of pore ice melting. The critical temperature sufficient for gas hydrate dissociation varies from −3.0 to −0.3 °C and depends on lithology (particle size) and salinity of the host frozen sediments. Taking into account an almost gradientless temperature distribution during degradation of subsea permafrost, even minor temperature increases can be expected to trigger large-scale dissociation of intrapermafrost hydrates. The ensuing active methane emission from the Arctic shelf sediments poses risks of geohazard and negative environmental impacts.

Destabilization of intrapermafrost gas hydrate is one possible reason for methane emission on the Arctic shelf. The formation of these intrapermafrost gas hydrates could occur almost simultaneously with the permafrost sediments due to the occurrence of a hydrate stability zone after sea regression and the subsequent deep cooling and freezing of sediments. The top of the gas hydrate stability zone could exist not only at depths of 200–250 m, but also higher due to local pressure increase in gas-saturated horizons during freezing. Formed at a shallow depth, intrapermafrost gas hydrates could later be preserved and transform into a metastable (relict) state. Under the conditions of submarine permafrost degradation, exactly relict hydrates located above the modern gas hydrate stability zone will, first of all, be involved in the decomposition process caused by negative temperature rising, permafrost thawing, and sediment salinity increasing. That’s why special experiments were conducted on the interaction of frozen sandy sediments containing relict methane hydrates with salt solutions of different concentrations at negative temperatures to assess the conditions of intrapermafrost gas hydrates dissociation. Experiments showed that the migration of salts into frozen hydrate-containing sediments activates the decomposition of pore gas hydrates and increase the methane emission. These results allowed for an understanding of the mechanism of massive methane release from bottom sediments of the East Siberian Arctic shelf.

The active emission of gas (mainly methane) from terrestrial and subsea permafrost in the Russian Arctic has been confirmed by ample evidence. In this paper, a generalization and some systematization of gas manifestations recorded in the Russian Arctic is carried out. The published data on most typical gas emission cases have been summarized in a table and illustrated by a map. The tabulated data include location, signatures, and possible sources of each gas show, with respective references. All events of onshore and shelf gas release are divided into natural and man-caused. and the natural ones are further classified as venting from lakes or explosive emissions in dryland conditions that produce craters on the surface. Among natural gas shows on land, special attention is paid to the emission of natural gas from Arctic lakes, as well as gas emissions with craters formation. In addition, a description of the observed man-caused gas manifestations associated with the drilling of geotechnical and production wells in the Arctic region is given. The reported evidence demonstrates the effect of permafrost degradation on gas release, especially in oil and gas fields.

Salt migration may be another reason why pore-gas hydrates dissociate in permafrost, besides pressure and temperature changes. Temperature variations in frozen hydrate-saturated sediments interacting with a NaCl solution have been studied experimentally at a constant temperature, ~−6 °C typical for permafrost. The experiments with frozen sandy samples containing metastable methane hydrate show that the migration of Na+ ions in the NaCl solution and their accumulation in the sediments can induce heat-consuming hydrate dissociation and ice melting. The hydrate-saturated frozen soils cool down at higher rates than their hydrate-free counterparts and require more time to recover their initial temperature. The temperature effects in hydrate-saturated frozen sediments exposed to contact with NaCl solutions depend strongly on salt concentration. The experimental results are used to model phase changes in the pore space associated with salt-ions transport and provide insights into the reasons for temperature changes.

Migration of dissolved salts from natural (cryopeg brines, seawater, etc.), or artificial sources can destabilize intrapermafrost gas hydrates. Salt transport patterns vary as a function of gas pressure, temperature, salinity, etc. The sensitivity of the salt migration and hydrate dissociation processes to ambient temperature and to the concentration and chemistry of saline solutions is investigated experimentally on frozen sand samples at a constant negative temperature (−6 °С). The experiments show that the ambient temperature and the solution chemistry control the critical salt concentration required for complete gas hydrate dissociation. Salt ions migrate faster from more saline solutions at higher temperatures, and the pore moisture can reach the critical salinity in a shorter time. The flux density and contents of different salt ions transported to the samples increase in the series Na2SO4–KCl–CaCl2–NaCl–MgCl2. A model is suggested to account for phase transitions of pore moisture in frozen hydrate-saturated sediments exposed to contact with concentrated saline solutions at pressures above and below the thermodynamic equilibrium, in stable and metastable conditions of gas hydrates, respectively.