Biogeochemical and historical drivers of microbial community composition and structure in sediments from Mercer Subglacial Lake, West Antarctica.

Ice streams that flow into Ross Ice Shelf are underlain by water-saturated sediments, a dynamic hydrological system, and subglacial lakes that intermittently discharge water downstream across grounding zones of West Antarctic Ice Sheet (WAIS). A 2.06 m composite sediment profile was recently recovered from Mercer Subglacial Lake, a 15 m deep water cavity beneath a 1087 m thick portion of the Mercer Ice Stream.

Global fjords as transitory reservoirs of labile organic carbon modulated by organo-mineral interactions.

The global carbon cycle is strongly modulated by organic carbon (OC) sequestration and decomposition. Whereas OC sequestration is relatively well constrained, there are few quantitative estimates of its susceptibility to decomposition. Fjords are hot spots of sedimentation and OC sequestration in marine sediments.

Mapping spatial and temporal variation of seafloor organic matter ΔC and δC in the Northern Gulf of Mexico following the Deepwater Horizon Oil Spill.

Following the Deepwater Horizon oil spill of 2010, large amounts of biodegraded oil (petrocarbon) sank to the seafloor. Our objectives were to 1) determine post-spill isotopic values as the sediments approached a new baseline and 2) track the recovery of affected sediments. Sediment organic carbon δC and ΔC reached a post-spill baseline averaging -21.

Microbial Fe(III) reduction as a potential iron source from Holocene sediments beneath Larsen Ice Shelf.

Recent recession of the Larsen Ice Shelf C has revealed microbial alterations of illite in marine sediments, a process typically thought to occur during low-grade metamorphism. In situ breakdown of illite provides a previously-unobserved pathway for the release of dissolved Fe to porewaters, thus enhancing clay-rich Antarctic sub-ice shelf sediments as an important source of Fe to Fe-limited surface Southern Ocean waters during ice shelf retreat after the Last Glacial Maximum. When sediments are underneath the ice shelf, Fe from microbial reductive dissolution of illite/Fe-oxides may be exported to the water column.

Petrocarbon evolution: Ramped pyrolysis/oxidation and isotopic studies of contaminated oil sediments from the Deepwater Horizon oil spill in the Gulf of Mexico.

Hydrocarbons released during the Deepwater Horizon (DWH) oil spill weathered due to exposure to oxygen, light, and microbes. During weathering, the hydrocarbons' reactivity and lability was altered, but it remained identifiable as "petrocarbon" due to its retention of the distinctive isotope signatures (14C and 13C) of petroleum. Relative to the initial estimates of the quantity of oil-residue deposited in Gulf sediments based on 2010-2011 data, the overall coverage and quantity of the fossil carbon on the seafloor has been attenuated.

Compositional and beam-size-dependent effects on pressure baseline in clumped isotope mass spectrometry.

Rationale: The analysis of carbonate samples for the application of clumped isotopes to paleoclimate reconstruction necessitates smaller beam intensities. However, there is a relationship between beam intensity and pressure-dependent baseline (PBL), and therefore between beam intensity and the correction for PBL. Here we explain the relationship between PBL and beam intensity to develop a better correction protocol and an improved understanding of clumped isotope mass spectrometry.

A centuries-long delay between a paleo-ice-shelf collapse and grounding-line retreat in the Whales Deep Basin, eastern Ross Sea, Antarctica.

Recent thinning and loss of Antarctic ice shelves has been followed by near synchronous acceleration of ice flow that may eventually lead to sustained deflation and significant contraction in the extent of grounded and floating ice. Here, we present radiocarbon dates from foraminifera that constrain the time elapsed between a previously described paleo-ice-shelf collapse and the subsequent major grounding-line retreat in the Whales Deep Basin (WDB) of eastern Ross Sea. The dates indicate that West Antarctic Ice Sheet (WAIS) grounding-line retreat from the continental shelf edge was underway prior to 14.

Hydrocarbon degradation and response of seafloor sediment bacterial community in the northern Gulf of Mexico to light Louisiana sweet crude oil.

The Deepwater Horizon (DWH) blowout resulted in the deposition to the seafloor of up to 4.9% of 200 million gallons of oil released into the Gulf of Mexico. The petroleum hydrocarbon concentrations near the wellhead were high immediately after the spill, but returned to background levels a few years after the spill.

Petroleum hydrocarbon persistence following the Deepwater Horizon oil spill as a function of shoreline energy.

An important aspect of oil spill science is understanding how the compounds within spilled oil, especially toxic components, change with weathering. In this study we follow the evolution of petroleum hydrocarbons, including n-alkanes, polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs, on a Louisiana beach and salt marsh for three years following the Deepwater Horizon spill. Relative to source oil, we report overall depletion of low molecular weight n-alkanes and PAHs in all locations with time.

Sediment Core Extrusion Method at Millimeter Resolution Using a Calibrated, Threaded-rod.

Aquatic sediment core subsampling is commonly performed at cm or half-cm resolution. Depending on the sedimentation rate and depositional environment, this resolution provides records at the annual to decadal scale, at best. An extrusion method, using a calibrated, threaded-rod is presented here, which allows for millimeter-scale subsampling of aquatic sediment cores of varying diameters.

Distributions and accumulation rates of polycyclic aromatic hydrocarbons in the northern Gulf of Mexico sediments.

Sediment samples collected from shelf, slope and interior basin of the northern Gulf of Mexico during 2011-2013, 1-3 years after the Deepwater Horizon (DWH) oil spill, were utilized to characterize PAH pollution history, in this region. Results indicate that the concentrations of surface ΣPAH43 and their accumulation rates vary between 44 and 160 ng g(-1) and 6-55 ng cm(-2) y(-1), respectively. ΣPAH43 concentration profiles, accumulation rates and Δ(14)C values are significantly altered only for the sediments in the immediate vicinity of the DWH wellhead.

Using natural abundance radiocarbon to trace the flux of petrocarbon to the seafloor following the Deepwater Horizon oil spill.

In 2010, the Deepwater Horizon accident released 4.6–6.0 × 10(11) grams or 4.

Blank corrections for ramped pyrolysis radiocarbon dating of sedimentary and soil organic carbon.

Ramped pyrolysis (RP) targets distinct components of soil and sedimentary organic carbon based on their thermochemical stabilities and allows the determination of the full spectrum of radiocarbon ((14)C) ages present in a soil or sediment sample. Extending the method into realms where more precise ages are needed or where smaller samples need to be measured involves better understanding of the blank contamination associated with the method. Here, we use a compiled data set of RP measurements of samples of known age to evaluate the mass of the carbon blank and its associated (14)C signature, and to assess the performance of the RP system.

Varying relative degradation rates of oil in different forms and environments revealed by ramped pyrolysis.

Degradation of oil contamination yields stabilized products by removing and transforming reactive and volatile compounds. In contaminated coastal environments, the processes of degradation are influenced by shoreline energy, which increases the surface area of the oil as well as exchange between oil, water, sediments, microbes, oxygen, and nutrients. Here, a ramped pyrolysis carbon isotope technique is employed to investigate thermochemical and isotopic changes in organic material from coastal environments contaminated with oil from the 2010 BP Deepwater Horizon oil spill.

Measurement of multiply substituted isotopologues ('clumped isotopes') of CO2 using a 5 kV compact isotope ratio mass spectrometer: performance, reference frame, and carbonate paleothermometry.

Rationale: The burgeoning field of 'clumped isotope' paleothermometry, which has broad applications in geosciences, depends almost entirely on measurements made on two types of mass spectrometer with the same ion source design. Demonstration that these measurements can be carried out on a retrofitted mass spectrometer with a different type of ion source is important to the growing community of geoscientists considering employing this technique.

Methods: We summarize the sample preparation techniques, mass spectrometry, and data processing involved in establishing an absolute reference frame for the measurement of Δ47 in CO2 from carbonate minerals using a prototype 5 kV mass spectrometer.

Accelerator mass spectrometry 14C determination in CO2 produced from laser decomposition of aragonite.

The determination of (14)C in aragonite (CaCO(3)) decomposed thermally to CO(2) using an yttrium-aluminum-garnet doped neodymium laser is reported. Laser decomposition accelerator mass spectrometry (LD-AMS) measurements reproduce AMS determinations of (14)C from the conventional reaction of aragonite with concentrated phosphoric acid. The lack of significant differences between these sets of measurements indicates that LD-AMS radiocarbon dating can overcome the significant fractionation that has been observed during stable isotope (C and O) laser decomposition analysis of different carbonate minerals.