Geology topics

John D. Kessler

Publications and source records attributed to John D. Kessler.

8 recordsLinked to original sources

USGS2022

Negligible atmospheric release of methane from decomposing hydrates in mid-latitude oceans

Naturally occurring gas hydrates may contribute to a positive feedback for global warming because they sequester large amounts of the potent greenhouse gas methane in ice-like deposits that could be destabilized by increasing ocean/atmospheric temperatures. Most hydrates occur within marine sediments; gas liberated during the decomposition of seafloor hydrates or originating with other methane pools can feed methane emissions at cold seeps. Regardless of the origin of seep methane, all previous measurements of methane emitted from seeps have shown it to have a unique fossil radiocarbon signature, contrasting with other sources of marine methane. Here we present the concentration and natural radiocarbon content of methane dissolved in the water column from the seafloor to the sea surface at seep fields along the US Atlantic and Pacific margins. For shallower water columns, where the seafloor is not within the hydrate stability zone, we do document seep CH 4 in some surface-water samples. However, measurements in deeper water columns along the US Atlantic margin reveal no evidence of seep CH 4 reaching surface waters when the water-column depth is greater than 430 ± 90 m. Gas hydrates exist only at water depths greater than ~550 m in this region, suggesting that the source of methane escaping to the atmosphere is not from hydrate decomposition.

North Carolina, Oregon, Virginia, Washington↗

USGS2022

Elevated levels of radiocarbon in methane dissolved in seawater reveal likely local contamination from nuclear powered vessels

Measurements of the natural radiocarbon content of methane ( 14 C-CH 4 ) dissolved in seawater and freshwater have been used to investigate sources and dynamics of methane. However, during investigations along the Atlantic, Pacific, and Arctic Ocean Margins of the United States, as well as in the North American Great Lakes, some samples revealed highly elevated 14 C-CH 4 values, as much as 4–5 times above contemporary atmospheric 14 C-CH 4 levels. Natural production of the 14 CH 4 isotopologue is too low to cause these observations nor can it explain the variations in location and depth. Numerous lab and field validation tests and blanks, as well as the relatively small number of samples that display these elevated values, all suggest that these signals are not derived from an unknown procedural issue. Here we suggest that the byproducts of nuclear power generation include localized discharges of the 14 CH 4 isotopologue into marine and aquatic environments, severely altering the measured 14 C-CH 4 isotopic signals. Since several of our sample sites are distant from on-land nuclear powerplants, we conduct further calculations concluding that the most elevated anomalies in 14 C-CH 4 likely originate with discharge from nuclear-powered vessels.

Maryland, North Carolina, Oregon, Virginia, Washin↗

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

Ideas and perspectives: A strategic assessment of methane and nitrous oxide measurements in the marine environment

>In the current era of rapid climate change, accurate characterization of climate-relevant gas dynamics – namely production, consumption, and net emissions – is required for all biomes, especially those ecosystems most susceptible to the impact of change. Marine environments include regions that act as net sources or sinks for numerous climate-active trace gases including methane (CH4) and nitrous oxide (N2O). The temporal and spatial distributions of CH4 and N2O are controlled by the interaction of complex biogeochemical and physical processes. To evaluate and quantify how these mechanisms affect marine CH4 and N2O cycling requires a combination of traditional scientific disciplines including oceanography, microbiology, and numerical modeling. Fundamental to these efforts is ensuring that the datasets produced by independent scientists are comparable and interoperable. Equally critical is transparent communication within the research community about the technical improvements required to increase our collective understanding of marine CH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB) was organized to enhance dialogue and collaborations pertaining to marine CH4 and N2O. Here, we summarize the outcomes from the workshop to describe the challenges and opportunities for near-future CH4 and N2O research in the marine environment.

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↗

USGS2018

Limited contribution of ancient methane to surface waters of the U.S. Beaufort Sea shelf

In response to warming climate, methane can be released to Arctic Ocean sediment and waters from thawing subsea permafrost and decomposing methane hydrates. However, it is unknown whether methane derived from this sediment storehouse of frozen ancient carbon reaches the atmosphere. We quantified the fraction of methane derived from ancient sources in shelf waters of the U.S. Beaufort Sea, a region that has both permafrost and methane hydrates and is experiencing significant warming. Although the radiocarbon-methane analyses indicate that ancient carbon is being mobilized and emitted as methane into shelf bottom waters, surprisingly, we find that methane in surface waters is principally derived from modern-aged carbon. We report that at and beyond approximately the 30-m isobath, ancient sources that dominate in deep waters contribute, at most, 10 ± 3% of the surface water methane. These results suggest that even if there is a heightened liberation of ancient carbon–sourced methane as climate change proceeds, oceanic oxidation and dispersion processes can strongly limit its emission to the atmosphere.

Science Advances↗

USGS2017

The interaction of climate change and methane hydrates

Gas hydrate, a frozen, naturally-occurring, and highly-concentrated form of methane, sequesters significant carbon in the global system and is stable only over a range of low-temperature and moderate-pressure conditions. Gas hydrate is widespread in the sediments of marine continental margins and permafrost areas, locations where ocean and atmospheric warming may perturb the hydrate stability field and lead to release of the sequestered methane into the overlying sediments and soils. Methane and methane-derived carbon that escape from sediments and soils and reach the atmosphere could exacerbate greenhouse warming. The synergy between warming climate and gas hydrate dissociation feeds a popular perception that global warming could drive catastrophic methane releases from the contemporary gas hydrate reservoir. Appropriate evaluation of the two sides of the climate-methane hydrate synergy requires assessing direct and indirect observational data related to gas hydrate dissociation phenomena and numerical models that track the interaction of gas hydrates/methane with the ocean and/or atmosphere. Methane hydrate is likely undergoing dissociation now on global upper continental slopes and on continental shelves that ring the Arctic Ocean. Many factors—the depth of the gas hydrates in sediments, strong sediment and water column sinks, and the inability of bubbles emitted at the seafloor to deliver methane to the sea-air interface in most cases—mitigate the impact of gas hydrate dissociation on atmospheric greenhouse gas concentrations though. There is no conclusive proof that hydrate-derived methane is reaching the atmosphere now, but more observational data and improved numerical models will better characterize the climate-hydrate synergy in the future.

Reviews of Geophysics↗

USGS2016

Determining the flux of methane into Hudson Canyon at the edge of methane clathrate hydrate stability

Methane seeps were investigated in Hudson Canyon, the largest shelf-break canyon on the northern US Atlantic Margin. The seeps investigated are located at or updip of the nominal limit of methane clathrate hydrate stability. The acoustic identification of bubble streams was used to guide water column sampling in a 32 km2 region within the canyon's thalweg. By incorporating measurements of dissolved methane concentration with methane oxidation rates and current velocity into a steady-state box model, the total emission of methane to the water column in this region was estimated to be 12 kmol methane per day (range: 6 – 24 kmol methane per day). These analyses suggest this methane is largely retained inside the canyon walls below 300 m water depth, and that it is aerobically oxidized to near completion within the larger extent of Hudson Canyon. Based on estimated methane emissions and measured oxidation rates, the oxidation of this methane to dissolved CO2 is expected to have minimal influences on seawater pH. This article is protected by copyright. All rights reserved.

Geochemistry, Geophysics, Geosystems↗