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Climate warming is expected to accelerate peatland degradation and release rates of carbon dioxide (CO2) and methane (CH4). Spruce and Peatlands Responses Under Changing Environments is an ecosystem-scale climate manipulation experiment, designed to examine peatland ecosystem response to climate forcings. We examined whether heating up to +9 °C to 3 m-deep in a peat bog over a 7-year period led to higher C turnover and CO2 and CH4 emissions, by measuring 14C of solid peat, dissolved organic carbon (DOC), CH4, and dissolved CO2 (DIC). DOC, a major substrate for heterotrophic respiration, increased significantly with warming. There was no 7-year trend in the DI14 C of the ambient plots which remained similar to their DO14 C. At +6.75 °C and +9 °C, the 14C of DIC, a product of microbial respiration, initially resembled ambient plots but became more depleted over 7 years of warming. We attributed the shifts in DI14 C to the increasing importance of solid phase peat as a substrate for microbial respiration and quantified this shift via the radiocarbon mass balance. The mass-balance model revealed increases in peat-supported respiration of the catotelm depths in heated plots over time and relative to ambient enclosures, from a baseline of 20%–25% in ambient enclosures, to 35%–40% in the heated plots. We find that warming stimulates microorganisms to respire ancient peat C, deposited under prior climate (cooler) conditions. This apparent destabilization of the large peat C reservoir has implications for peatland-climate feedbacks especially if the balance of the peatland is tipped from net C sink to C source.

Following the Deepwater Horizon oil spill (DWHOS), the formation of an unexpected and extended sedimentation event of oil-associated marine snow (MOSSFA: Marine Oil Snow Sedimentation and Flocculent Accumulation) demonstrated the importance of biology on the fate of contaminants in the oceans. We used a wide range of compound-specific data (aliphatics, hopanes, steranes, triaromatic steroids, polycyclic aromatics) to chemically characterize the MOSSFA event containing abundant and multiple hydrocarbon sources (e.g., oil residues and phytoplankton). Sediment samples were collected in 2010–2011 (ERMA-NRDA programs: Environmental Response Management Application – Natural Resource Damage Assessment) and 2018 (REDIRECT project: Resuspension, Redistribution and Deposition of Deepwater Horizon recalcitrant hydrocarbons to offshore depocenter) in the northern Gulf of Mexico to assess the role of biogenic and chemical processes on the fate of oil residues in sediments. The chemical data revealed the deposition of the different hydrocarbon mixtures observed in the water column during the DWHOS (e.g., oil slicks, submerged-plumes), defining the chemical signature of MOSSFA relative to where it originated in the water column and its fate in deep-sea sediments. MOSSFA from surface waters covered 90% of the deep-sea area studied and deposited 32% of the total oil residues observed in deep-sea areas after the DWHOS while MOSSFA originated at depth from the submerged plumes covered only 9% of the deep-sea area studied and was responsible for 15% of the total deposition of oil residues. In contrast, MOSSFA originated at depth from the water column covered only 1% of the deep-sea area studied (mostly in close proximity of the DWH wellhead) but was responsible for 53% of the total deposition of oil residues observed after the spill in this area. This study describes, for the first time, a multi-chemical method for the identification of biogenic and oil-derived inputs to deep-sea sediments, critical for improving our understanding of carbon inputs and storage at depth in open ocean systems.

The focus of this study was to determine the long-term fate of oil-residues from the 2010 Deepwater Horizon (DwH) oil spill due to remobilization, transport, and re-distribution of oil residue contaminated sediments to down-slope depocenters following initial deposition on the seafloor. We characterized hydrocarbon residues, bulk sediment organic matter, ease of resuspension, sedimentology, and accumulation rates to define distribution patterns in a 14,300 km2 area southeast of the DwH wellhead (1,500 to 2,600 m water depth). Oil-residues from the DwH were detected at low concentrations in 62% of the studied sites at specific sediment layers, denoting episodic deposition of oil-residues during 2010–2014 and 2015–2018 periods. DwH oil residues exhibited a spatial distribution pattern that did not correspond with the distribution of the surface oil slick, subsurface plume or original seafloor spatial expression. Three different regions were apparent in the overall study area and distinguished by the episodic nature of sediment accumulation, the ease of sediment resuspension, the timing of oil-residue deposition, carbon content and isotopic composition and foram fracturing extent. These data indicate that resuspension and down-slope redistribution of oil-residues occurred in the years following the DwH event and must be considered in determining the fate of the spilled oil deposited on the seafloor.

Suspended particulate organic carbon (POCsusp) in the Gulf of Mexico is unique compared to other seas and oceans. In addition to surface primary production, isotopic analysis indicates that microbial cycling of oil and riverine inputs are primary sources of carbon to POCsusp in the Gulf. To characterize POCsusp from seep sites and non-seep north central Gulf (NCG) sites potentially affected by the Deepwater Horizon (DWH) spill, we analyzed 277 and 123 samples for δ13C and Δ14C signatures, respectively. Depth, partitioned into euphotic (300 m), was the main driver of spatial δ13C differences, with deep depths exhibiting 13C depletion. Both deep depths and proximity to sources of natural seepage resulted in 14C depletion. A two-endmember mixing model based on Δ14C indicated that sources to POCsusp were 14–29% fossil carbon at NCG sites and 19–57% at seep sites, with the balance being modern surface production. A six-component Bayesian mixing model MixSIAR, using both 13C and 14C, suggested that riverine inputs were an important carbon source to POCsusp contributing 34–46%. The influence of seeps was localized. Below the euphotic zone at seep sites, 46 ± 5% (n = 9) of the carbon in POCsusp was derived from environmentally degraded, transformed oil; away from seeps, transformed oil contributed 15 ± 4% (n = 39). We hypothesized that, at NCG sites removed from hydrocarbon seep sources, isotopic signatures would be depleted following the spill and then shift towards background-like enriched values over time. At deep depths we observed decreasing Δ14C signatures in POCsusp from 2010 to 2012, followed by isotopic enrichment from 2012 to 2014 and a subsequent recovery rate of 159‰ per year, consistent with this hypothesis and with biodegraded material from DWH hydrocarbons contributing to POCsusp.

The Deepwater Horizon oil spill released petroleum hydrocarbons that were depleted in δ13C and Δ14C at depth into the Gulf of Mexico. Stable-carbon and radiocarbon isotopic values and high-resolution mass spectrometry were used to follow the distributions of this petroleum and to track its transformation into petrocarbon, a term used to describe crude oil or transformed crude oil following biodegradation, weathering, oxygenation, or loss of lighter components. The term petrocarbon includes oil- or methane-derived carbon assimilated or incorporated into microbial biomass or into the food web as well as degraded and undegraded petroleum constituents. Here we report (1) the increase in the relative abundance of oxygen-containing carbon compounds making up the dissolved organic matter (DOM) with increasing depth through the water column, indicating the biodegradation of DOM as it was transported to depth in the water column, (2) the finding of 14C depletion in DOM indicating petrocarbon inputs, and (3) the decrease and subsequent increase of 14C in the isotopic composition of sinking particles indicating the capture of petrocarbon in sediment traps. In addition, we discuss the 14C depletion of this material once it is sedimented to the seafloor and the implications for oil spill budgets of seafloor petrocarbon deposition.

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 δ13C and Δ14C reached a post-spill baseline averaging −21.2 ± 0.9‰ (n = 129) and −220 ± 66‰ (n = 95). Spatial variations in seafloor organic carbon baseline isotopic values, 13C and 14C, were influenced by river discharge and hydrocarbon seepage, respectively. Inverse Distance Weighting of surface sediment Δ14C values away from seep sites showed a 50% decrease in the total mass of petrocarbon, from 2010 to 2014. We estimated a rate of loss of −2 × 109 g of petrocarbon-C/year, 2–11% of the degradation rates in surface slicks. Despite the observed recovery in sediments, lingering residual material in the surface sediments was evident seven years following the blowout.

The Deepwater Horizon oil spill released a large volume of 13C and radiocarbon depleted organic matter to the northern Gulf of Mexico. Evidence of petroleum-derived carbon entering the offshore planktonic foodweb, as well as widespread oiling of coastal areas documented in previous studies suggests that hydrocarbons could have entered the near shore foodweb. To test this hypothesis, we measured radiocarbon (Δ14C%) and stable carbon isotopes (δ13C) in an assortment of fish tissue, invertebrate tissue and shell samples collected within a year of the spill at seven sites from Louisiana to Florida USA across the northern Gulf of Mexico. We observed a west–east gradient with the most depleted radiocarbon values found in Terrebonne Bay, Louisana and increasingly enriched radiocarbon values in organisms collected at sites to the east. Depleted radiocarbon values as low as −10% in invertebrate soft tissue from Terrebonne suggest assimilation of fossil carbon (2.8±1.2%), consistent with the hypothesis that organic matter from petrochemical reservoirs released during the Deepwater Horizon spill entered the coastal food web to a limited extent. Further there was a significant correlation between radiocarbon and δ13C values in invertebrate tissue consistent with this hypothesis. Both oyster tissue and hard head catfish tissue collected in impacted areas of coastal Louisiana were significantly depleted in 14C and 13C relative to organisms collected in the unaffected Apalachicola Bay, Florida (p

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. To analyze recovery of oil contaminated deep-sea sediments in the northern Gulf of Mexico we tracked the carbon isotopic composition (13C and 14C, radiocarbon) of bulk sedimentary organic carbon through time at 4 sites. Using ramped pyrolysis/oxidation, we determined the thermochemical stability of sediment organic matter at 5 sites, two of these in time series. There were clear differences between crude oil (which decomposed at a lower temperature during ramped oxidation), natural hydrocarbon seep sediment (decomposing at a higher temperature; Δ14C = -912‰) and our control site (decomposing at a moderate temperature; Δ14C = -189‰), in both the stability (ability to withstand ramped temperatures in oxic conditions) and carbon isotope signatures. We observed recovery toward our control site bulk Δ14C composition at sites further from the wellhead in ~4 years, whereas sites in closer proximity had longer recovery times. The thermographs also indicated temporal changes in the composition of contaminated sediment, with shifts towards higher temperature CO2 evolution over time at a site near the wellhead, and loss of higher temperature CO2 peaks at a more distant site.

The extensive release of oil during the 2010 Deepwater Horizon spill in the northern Gulf of Mexico perturbed the pelagic ecosystem and associated sinking material. To gauge the recovery and post-spill baseline sources, we measured Δ14C, δ13C and δ34S of sinking particles near the spill site and at a reference site and natural seep site. Particulates were collected August 2010–April 2016 in sediment traps moored at sites with depths of 1160–1660 m. Near the spill site, changes in Δ14C indicated a 3-year recovery period, while δ34S indicated 1–2 years, which agreed with estimates of 1–2 years based on hydrocarbon composition. Under post-spill baseline conditions, carbon inputs to sinking particulates in the northern Gulf were dominated by surface marine production (80–85%) and riverine inputs (15–20%). Near the spill site, Δ14C values were depleted in October 2010 (–140 to –80‰), increasing systematically by 0.07 ± 0.02‰ day–1 until July 2013 when values reached –3.2 ± 31.0‰. This Δ14C baseline was similar to particulates at the reference site (3.8 ± 31.1‰). At both sites, δ13C values stayed constant throughout the study period (–21.9 ± 0.5‰ and –21.9 ± 0.9‰, respectively). δ34S near the spill site was depleted (7.4 ± 3.1‰) during October 2010–September 2011, but enriched (16.9 ± 2.0‰) and similar to the reference site (16.2 ± 3.1‰) during November 2012–April 2015. At the seep site, Δ14C values were –21.7 ± 45.7‰ except during August 2012–January 2013 when a significant Δ14C depletion of –109.0 ± 29.1‰ was observed. We interpret this depletion period, also observed in δ13C data, as caused by the incorporation of naturally seeped oil into sinking particles. Determination of post-spill baselines for these isotopic signatures allows for evaluation of anthropogenic inputs in future.

Over 600 million liters of oil and copious amounts of methane were released into the Gulf of Mexico between April 20, 2010 and July 15, 2010. We used stable and radiocarbon analyses as a forensic tool to trace these hydrocarbons from the Deepwater Horizon (DwH) well into suspended particulate organic carbon (POCsusp), sinking particulate organic carbon (POCsink), and sedimentary organic carbon on the seafloor. POCsusp samples were considerably depleted both in δ13C and Δ14C relative to surface production, with δ13C and Δ14C values as low as −37.2‰ and −618‰, respectively. POCsink time series data revealed a modern Δ14C value due to a large diatom bloom in early September 2010, but values became depleted as oil contaminated particles continued to descend in the water column until the end of the year. Sediment cores collected in the vicinity of the DwH wellhead revealed evidence of oil contamination in the surface layer (0–1 cm), as indicated by a depletion in Δ14C values compared to the layers below the surface. In addition to providing evidence of oil contamination using stable and radiocarbon analyses, our study was consistent with the existence of a pathway by which spilled oil was deposited onto the seafloor.

In 2010, the Deepwater Horizon accident released 4.6–6.0 × 10(11) grams or 4.1 to 4.6 million barrels of fossil petroleum derived carbon (petrocarbon) as oil into the Gulf of Mexico. Natural abundance radiocarbon measurements on surface sediment organic matter in a 2.4 × 10(10) m(2) deep-water region surrounding the spill site indicate the deposition of a fossil-carbon containing layer that included 1.6 to 2.6 × 10(10) grams of oil-derived carbon. This quantity represents between 0.5 to 9.1% of the released petrocarbon, with a best estimate of 3.0–4.9%. These values may be lower limit estimates of the fraction of the oil that was deposited on the seafloor because they focus on a limited mostly deep-water area of the Gulf, include a conservative estimate of thickness of the depositional layer, and use an average background or prespill radiocarbon value for sedimentary organic carbon that produces a conservative value. A similar approach using hopane tracer estimated that 4–31% of 2 million barrels of oil that stayed in the deep sea settled on the bottom. Converting that to a percentage of the total oil that entered into the environment (to which we normalized our estimate) converts this range to 1.8 to 14.4%. Although extrapolated over a larger area, our independent estimate produced similar values.

Dissolved methane concentrations in the ocean are close to equilibrium with the atmosphere. Because methane is only sparingly soluble in seawater, measuring it without contamination is challenging for samples collected and processed in the presence of air. Several methods for analyzing dissolved methane are described in the literature, yet none has conducted a thorough assessment of the method yield, contamination issues during collection, transport and storage, and the effect of temperature changes and preservative. Previous extraction methods transfer methane from water to gas by either a "sparge and trap" or a "headspace equilibration" technique. The gas is then analyzed for methane by gas chromatography. Here, we revisit the headspace equilibration technique and describe a simple, inexpensive, and reliable method to measure methane in fresh and seawater, regardless of concentration. Within the range of concentrations typically found in surface seawaters (2-1000 nmol L-1), the yield of the method nears 100% of what is expected from solubility calculation following the addition of known amount of methane. In addition to being sensitive (detection limit of 0.1 ppmv, or 0.74 nmol L-1), this method requires less than 10 min per sample, and does not use highly toxic chemicals. It can be conducted with minimum materials and does not require the use of a gas chromatograph at the collection site. It can therefore be used in various remote working environments and conditions.

Seasonal hypoxia [dissolved oxygen (DO) ≤ 2 mg l−1] occurs over large regions of the northwestern Gulf of Mexico continental shelf during the summer months (June–August) as a result of nutrient enrichment from the Mississippi–Atchafalaya River system. We characterized the community structure of mobile fishes and invertebrates (i.e., nekton) in and around the hypoxic zone using 3 years of bottom trawl and hydrographic data. Species richness and total abundance were lowest in anoxic waters (DO ≤ 1 mg l−1) and increased at intermediate DO levels (2–4 mg l−1). Species were primarily structured as a benthic assemblage dominated by Atlantic croaker (Micropogonias undulatus) and sand and silver seatrout (Cynoscion spp.), and a pelagic assemblage dominated by Atlantic bumper (Chloroscombrus chrysurus). Of the environmental variables examined, bottom DO and distance to the edge of the hypoxic zone were most strongly correlated with assemblage structure, while temperature and depth were important in some years. Hypoxia altered the spatial distribution of both assemblages, but these effects were more severe for the benthic assemblage than for the pelagic assemblage. Brown shrimp, the primary target of the commercial shrimp trawl fishery during the summer, occurred in both assemblages, but was more abundant within the benthic assemblage. Given the similarity of the demersal nekton community described here to that taken as bycatch in the shrimp fishery, our results suggest that hypoxia-induced changes in spatial dynamics have the potential to influence harvest and bycatch interactions in and around the Gulf hypoxic zone.

In contrast to other oligotrophic water bodies the Gulf of Mexico (GOM) hosts an abundance of hydrocarbon seeps, which likely influences the microbial assemblages it hosts particularly regarding the availability of labile carbon in the aphotic GOM. The aphotic zone receives direct injection of seep methane (CH4), but CH4 from an unknown source has been reported at supersaturated concentrations relative to the atmosphere in the GOM photic zone. Here we used iTag sequencing of 16S rRNA genes to characterize GOM microbial communities and to relate changes in microbial community structure to the properties inherent to their oceanic province-seafloor to the photic zone, seep and non-seep. Along this trajectory water column communities were distinct in the euphotic zone compared to the mesopelagic and deep-sea. In the euphotic zone the relative abundance of a cyanobacterial species (Prochlorococcus) was significantly correlated with both CH4 and chlorophyll a concentrations and was abundant in some deep-chlorophyll maximum (DCM) samples. The relative abundance of microorganisms related to known hydrocarbon degraders were also significantly correlated with CH4 in the euphotic zone, but no canonical methanotrophs were observed. In the mesopelagic to the seafloor canonical methanotrophs were identified, but only a Marine Group II Euryarchaeota was significantly correlated with CH4. Overall, depth and the associated environmental conditions were the primary drivers in structuring microbial communities over the GOM water column. Further, CH4 concentrations and relative microbial abundances covaried significantly from the seafloor to the photic zone in the GOM. The lack of a significant relationship between canonical methanotrophs and CH4 in the aphotic zone, even when sampling at seep sites, may suggest methane-oxidation by unknown microorganisms. Similarly their absence in the CH4 maximum and DCM suggested that CH4 is either oxidized by unrecognized methanotrophs or escapes the CH4 biofilter and fluxes to the atmosphere.

Cet article analyse les reactions parentales face aux developpements non conformes du genre de leur enfant et avance que les mandats parentaux de protection et d’acceptation deviennent problematiques du fait des differences qui existent entre les normes de genre de l’enfant et celles de sa famille, aussi bien qu’entre celles de l’enfant et celles de son environnement. Au travers de multiples modalites therapeutiques – education et accompagnement parental, groupes de soutien de parents, therapie de l’enfant et therapie familiale – l’auteur illustre des interventions soutenant a la fois les parents et les enfants pre-puberes dans leur facon de negocier les liens familiaux et la fluidite du genre.

The Deepwater Horizon (Macondo) oil spill released large volumes of oil and gas of distinct carbon isotopic composition to the northern Gulf of Mexico, allowing Graham et al (2010 Environ. Res. Lett. 5 045301) to use stable carbon isotopes (δ13C) to infer the introduction of spilled oil into the planktonic food web. Surface ocean organic production and measured oil are separated by 5–7‰ in stable carbon isotope (δ13C) space, while in radiocarbon (Δ14C) space these two potential sources are separated by more than 1000‰. Thus radiocarbon isotopes provide a more sensitive tracer by which to infer possible introduction of Macondo oil into the food web. We measured Δ14C and δ13C in plankton collected from within 100 km of the spill site as well as in coastal and offshore DIC (dissolved inorganic carbon or ΣCO2) to constrain surface production values. On average, plankton values were depleted in 14C relative to surface DIC, and we found a significant linear correlation between Δ14C and δ13C in plankton. Cumulatively, these results are consistent with the hypothesis that carbon released from the Deepwater Horizon spill contributed to the offshore planktonic food web. Our results support the findings of Graham et al (2010 Environ. Res. Lett. 5 045301), but we infer that methane input may be important.