Search Results (3)

The Tuaheni Landslide Complex, located on the upper slope of the northern Hikurangi Margin in New Zealand, is a unique place to research on slow slip creep-like deformation and seabed failure, as well as their possible relationship with the presence of gas hydrates, cold seeps, and fluid migration. Based on the visual interpretation of seismic data, it is sometimes very difficult to identify various subsurface structures and tectonic features. We study certain seismic attributes, namely the reflection strength, instantaneous frequency, instantaneous phase, and the Hilbert transform, in the Tuaheni Landslide Complex and observe that these attributes play a very important role in identifying and interpreting various subsurface geological features and bed boundaries that are not clearly visible in the seismic sections. In general, these seismic attributes are studied to identify hydrocarbons such as oil and gas. However, in this present study these seismic attributes nicely illustrate the fluid migration pathways, the decollement of the sediment slide, the base of the debris flow, the base of the deformed sediment and gas migration, etc., along two perpendicular seismic profiles crossing the Site U1517 of IODP Expedition 372. The instantaneous phase and Hilbert transform attribute depict the bed boundaries and discontinuities, whereas the reflection strength and instantaneous frequency attributes characterize the various strata in terms of whether they are associated with fluid at their bases. The possible role of tectonic activity and seafloor slope failure due to gas hydrate dissociation and vice versa is clearly visible through fluid-filled weak zones in the seismic attribute volumes. Gas hydrates are dissociating and BSRs are abruptly pinching out towards the seafloor due to the movement of hot fluid and free gas, enhancing seafloor sliding and local tectonic activities together. Full article

We compare sediment vertical methane flux off the Mahia Peninsula, on the Hikurangi Margin, east of New Zealand’s North Island, with a combination of geochemical, multichannel seismic and sub-bottom profiler data. Stable carbon isotope data provided an overview of methane contributions to shallow sediment carbon pools. Methane varied considerably in concentration and vertical flux across stations in close proximities. At two Mahia transects, methane profiles correlated well with integrated seismic and TOPAS data for predicting vertical methane migration rates from deep to shallow sediment. However, at our “control site”, where no seismic blanking or indications of vertical gas migration were observed, geochemical data were similar to the two Mahia transect lines. This apparent mismatch between seismic and geochemistry data suggests a potential to underestimate gas hydrate volumes based on standard seismic data interpretations. To accurately assess global gas hydrate deposits, multiple approaches for initial assessment, e.g., seismic data interpretation, heatflow profiling and controlled-source electromagnetics, should be compared to geochemical sediment and porewater profiles. A more thorough data matrix will provide better accuracy in gas hydrate volume for modeling climate change and potential available energy content. Full article

Moderate elevated vertical methane (CH₄) flux is associated with sediment accretion and raised fluid expulsion at the Hikurangi subduction margin, located along the northeast coast of New Zealand. This focused CH₄ flux contributes to the cycling of inorganic and organic carbon in solid phase sediment and pore water. Along a 7 km offshore transect across the Porangahau Ridge, vertical CH₄ flux rates range from 11.4 mmol·m⁻²·a⁻¹ off the ridge to 82.6 mmol·m⁻²·a⁻¹ at the ridge base. Stable carbon isotope ratios (δ¹³C) in pore water and sediment were variable across the ridge suggesting close proximity of heterogeneous carbon sources. Methane stable carbon isotope ratios ranging from −107.9‰ to −60.5‰ and a C1:C2 of 3000 indicate a microbial, or biogenic, source. Near ridge, average δ¹³C for pore water and sediment inorganic carbon were ¹³C-depleted (−28.7‰ and −7.9‰, respectively) relative to all core subsamples (−19.9‰ and −2.4‰, respectively) suggesting localized anaerobic CH₄ oxidation and precipitation of authigenic carbonates. Through the transect there was low contribution from anaerobic oxidation of CH₄ to organic carbon pools; for all cores δ¹³C values of pore water dissolved organic carbon and sediment organic carbon averaged −24.4‰ and −22.1‰, respectively. Anaerobic oxidation of CH₄ contributed to pore water and sediment organic carbon near the ridge as evidenced by carbon isotope values as low as to −42.8‰ and −24.7‰, respectively. Carbon concentration and isotope analyses distinguished contributions from CH₄ and phytodetrital carbon sources across the ridge and show a low methane contribution to organic carbon. Full article