Mihai Leonte | Geology Reports

USGS2021

Estimating the impact of seep methane oxidation on ocean pH and dissolved inorganic radiocarbon along the U.S. mid‐Atlantic Bight

Ongoing ocean warming can release methane (CH 4 ) currently stored in ocean sediments as free gas and gas hydrates. Once dissolved in ocean waters, this CH 4 can be oxidized to carbon dioxide (CO 2 ). While it has been hypothesized that the CO 2 produced from aerobic CH 4 oxidation could enhance ocean acidification, a previous study conducted in Hudson Canyon shows that CH 4 oxidation has a small short‐term influence on ocean pH and dissolved inorganic radiocarbon. Here we expand upon that investigation to assess the impact of widespread CH 4 seepage on CO 2 chemistry and possible accumulation of this carbon injection along 234 km of the U.S. Mid‐Atlantic Bight. Consistent with the estimates from Hudson Canyon, we demonstrate that a small fraction of ancient CH 4 ‐derived carbon is being assimilated into the dissolved inorganic radiocarbon (mean fraction of 0.5 ± 0.4 %). The areas with the highest fractions of ancient carbon coincide with elevated CH 4 concentration and active gas seepage. This suggests that aerobic CH 4 oxidation has a greater influence on the dissolved inorganic pool in areas where CH 4 concentrations are locally elevated, instead of displaying a cumulative effect downcurrent from widespread groupings of CH 4 seeps. An upper limit approximation of the input rate of ancient‐derived DIC into the waters overlying the northern U. S Mid‐Atlantic Bight further suggests that oxidation of ancient CH 4 ‐derived carbon is not negligible on the global scale and could contribute to deep‐water acidification over longer time scales.

Journal of Geophysical Research- Biogeosciences↗

USGS2020

Surface methane concentrations along the mid-Atlantic bight driven by aerobic subsurface production rather than seafloor gas seeps

Relatively minor amounts of methane, a potent greenhouse gas, are currently emitted from the oceans to the atmosphere, but such methane emissions have been hypothesized to increase as oceans warm. Here, we investigate the source, distribution, and fate of methane released from the upper continental slope of the U.S. Mid-Atlantic Bight, where hundreds of gas seeps have been discovered between the shelf-break and ~1600 m water depth. Using physical, chemical, and isotopic analyses, we identify two main sources of methane in the water column: seafloor gas seeps and in situ aerobic methanogenesis which primarily occurs at 100 – 200 m depth in the water column. Stable isotopic analyses reveal that water samples collected at all depths were significantly impacted by aerobic methane oxidation, the dominant methane sink in this region, with more than 50% of the methane being oxidized, on average. Due to methane oxidation in the deeper water column, below 200 m depth, surface concentrations of methane are influenced more by methane sources found near the surface (0 – 10 m depth) and in the subsurface (10 - 200 m depth), rather than seafloor emissions at greater depths.

Atlantic margin↗