Prospects For Gulf of Mexico Environmental Recovery and Restoration

Previous oil spills provide clear evidence that ecosystem restoration efforts are challenging, and recovery can take decades. Similar to the Ixtoc 1 well blowout in 1979, the Deepwater Horizon (DWH) oil spill was enormous both in volume of oil spilled and duration, resulting in environmental impacts from the deep ocean to the Gulf of Mexico coastline. Data collected during the National Resource Damage Assessment showed significant damage to coastal areas (especially marshes), marine organisms, and deep-sea habitat. Previous spills have shown that disparate regions recover at different rates, with especially long-term effects in salt marshes and deepsea habitat. Environmental recovery and restoration in the northern Gulf of Mexico are dependent upon fundamental knowledge of ecosystem processes in the region. PostDWH research data provide a starting point for better understanding baselines and ecosystem processes. It is imperative to use the best science available to fully understand DWH environmental impacts and determine the appropriate means to ameliorate those impacts through restoration. Filling data gaps will be necessary to make better restoration decisions, and establishing new baselines will require long-term studies. Future research, especially via NOAA’s RESTORE Science Program and the state-based Centers of Excellence, should provide a path to understanding the potential for restoration and recovery of this vital marine ecosystem

Methane in the surface waters of the Arabian Sea

More than 2000 measurements of atmospheric and dissolved methane (CH44) were performed in the central and northwestern Arabian Sea as part of the German JGOFS Arabian Sea Process Study during three cruises in March, May/June, and June/July 1997. Mean CH4 saturations in the surface waters of the central Arabian Sea were in the range of 103–107%. Significantly enhanced saturations were observed in the coastal upwelling area at the coast of Oman (up to 156%) and in an upwelling filament (up to 145%). The CH4 surface concentrations in the upwelling area were negatively correlated to sea surface temperatures. Area‐weighted, seasonally adjusted estimates of the sea‐air fluxes of CH4 gave annual emissions from the Arabian Sea of 11–20 Gg CH4, suggesting that previously reported very high surface CH4 concentrations might be atypical owing to the interannual variability of the Arabian Sea and that the emissions derived from them are probably overestimates

Methane in the Baltic and North Seas and a reassessment of the marine emissions of methane

During three measurement campaigns on the Baltic and North Seas, atmospheric and dissolved methane was determined with an automated gas chromatographic system. Area-weighted mean saturation values in the sea surface waters were 113 ± 5% and 395 ± 82% (Baltic Sea, February and July 1992) and 126 ± 8% (south central North Sea, September 1992). On the bases of our data and a compilation of literature data the global oceanic emissions of methane were reassessed by introducing a concept of regional gas transfer coefficients. Our estimates computed with two different air-sea exchange models lie in the range of 11-18 Tg CH4 yr-1. Despite the fact that shelf areas and estuaries only represent a small part of the world's ocean they contribute about 75% to the global oceanic emissions. We applied a simple, coupled, three-layer model to numerically simulate the time dependent variation of the oceanic flux to the atmosphere. The model calculations indicate that even with increasing tropospheric methane concentration, the ocean will remain a source of atmospheric methane

Waterside convection and stratification control methane spreading in supersaturated Arctic fjords (Spitsbergen)

Seasonally ice covered in the past, the fjords in West Spitsbergen turn into being perennially ice free in the present. This feedback to Arctic amplification of global warming changes gas fluxes at the atmosphere-ocean interface. Furthermore, in this Polar region, coupled feedbacks likely enhance Arctic amplification of global warming as numerous gas seepages provide evidence for active gas emissions at the sediment-water interface. We present a time series (2015–2017) of dissolved methane concentrations combined with hydrographic data in Adventfjorden and Tempelfjorden, two sub-fjords of Isfjorden located at the west coast of Spitsbergen. While both sub-fjords remained permanently supersaturated, we detected pronounced temporal and spatial variations in the methane excess level. Our study revealed that seasonal water transformations were key to seasonally changing methane pathways including potential sea-air flux (efflux). We suggest that a cascade of feedback processes, seasonally triggered by waterside convection and stratification, adjusts the amount of methane released and transported within fjord water. When sea ice was missing, strong winter cooling affected the methane supersaturation in contrary directions: first a drop and then a strong increase. In early winter, convective mixing favoured efflux, which reduced the supersaturation. Later in winter, the thermal convection resulted in a continuous overturning of the water column. When the thermal convection reached the bottom, sediment resuspension by turbulence increased, which in turn encouraged enhanced methane release. Subsequently transported along vertical isopycnals, methane from the bottom water reached the water-atmosphere interface. These coupled events created a steady state, simultaneously maintaining supersaturation and efflux. During the warm season, the fjord water became stratified and methane transport occurred mainly laterally in the bottom water. The seasonally changing hydrographic conditions strongly triggered the methane spreading in both sub-fjords and point to a switch between the atmosphere and ocean as main sinks in winter and summer, respectively. Upcoming variations in seasonality, i.e. warmer/cooler summer compared to colder/warmer winter will influence these pathways and the final fate of methane discharged into Arctic fjords.publishedVersio

Dissolved methane distributions and air-sea flux in the plume of a massive seep field, Coal Oil Point, California

Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 34 (2007): L22603, doi:10.1029/2007GL031344.Large quantities of natural gas are emitted from the seafloor into the stratified coastal ocean near Coal Oil Point, Santa Barbara Channel, California. Methane was quantified in the down current surface water at 79 stations in a 280 km2 study area. The methane plume spread over an area of ~70 km2 and emitted on the order of 5 × 104 mol d−1 to the atmosphere. A monthly time series at 14 stations showed variable methane concentrations which were correlated with changing sub-mesoscale surface currents. Air-sea fluxes estimated from the time series indicate that the air-sea flux derived for the 280 km2 area is representative of the daily mean flux from this area. Only 1% of the dissolved methane originating from Coal Oil Point enters the atmosphere within the study area. Most of it appears to be transported below the surface and oxidized by microbial activity.The research was supported by the University of California Energy Institute and the National Science Foundation (OCE 0447395)

Prospects for gulf of Mexico environmental recovery and restoration

Previous oil spills provide clear evidence that ecosystem restoration efforts are challenging, and recovery can take decades. Similar to the Ixtoc 1 well blowout in 1979, the Deepwater Horizon (DWH) oil spill was enormous both in volume of oil spilled and duration, resulting in environmental impacts from the deep ocean to the Gulf of Mexico coastline. Data collected during the National Resource Damage Assessment showed significant damage to coastal areas (especially marshes), marine organisms, and deep-sea habitat. Previous spills have shown that disparate regions recover at different rates, with especially long-term effects in salt marshes and deepsea habitat. Environmental recovery and restoration in the northern Gulf of Mexico are dependent upon fundamental knowledge of ecosystem processes in the region. PostDWH research data provide a starting point for better understanding baselines and ecosystem processes. It is imperative to use the best science available to fully understand DWH environmental impacts and determine the appropriate means to ameliorate those impacts through restoration. Filling data gaps will be necessary to make better restoration decisions, and establishing new baselines will require long-term studies. Future research, especially via NOAA’s RESTORE Science Program and the state-based Centers of Excellence, should provide a path to understanding the potential for restoration and recovery of this vital marine ecosystem

Porewater methane transport within the gas vesicles of diurnally migrating Chaoborus spp.: An energetic advantage

We show that diurnally migrating Chaoborus sp. (phantom midge larvae), which can be highly abundant in eutrophic lakes with anoxic bottom, utilises sediment methane to inflate their tracheal sacs, which provides positive buoyancy to aid vertical migration. This process also effectively transports sediment methane bypassing oxidation to the upper water column, adding to the total methane outflux to the atmosphere

A water column study of methane around gas flares located at the West Spitsbergen continental margin

In the Arctic Seas, the West Spitsbergen continental margin represents a prominent methane seep area. In this area, free gas formation and gas ebullition as a consequence of hydrate dissociation due to global warming are currently under debate. Recent studies revealed shallow gas accumulation and ebullition of methane into the water column at more than 250 sites in an area of 665 km2. We conducted a detailed study of a subregion of this area, which covers an active gas ebullition area of 175 km2 characterized by 10 gas flares reaching from the seafloor at~245 m up to 50 m water depth to identify the fate of the released gas due to dissolution of methane from gas bubbles and subsequent mixing, transport and microbial oxidation. The oceanographic data indicated a salinity-controlled pycnocline situated ~20 m above the seafloor. A high resolution sampling program at the pycnocline at the active gas ebullition flare area revealed that the methane concentration gradient is strongly controlled by the pycnocline. While high methane concentrations of up to 524 nmol L−1 were measured below the pycnocline, low methane concentrations of less than 20 nmol L−1 were observed in the water column above. Variations in the δ13CCH4 values point to a 13C depleted methane source (~−60‰ VPDB) being mainly mixed with a background values of the ambient water (~−37.5‰ VPDB). A gas bubble dissolution model indicates that ~80% of the methane released from gas bubbles into the ambient water takes place below the pycnocline. This dissolved methane will be laterally transported with the current northwards and most likely microbially oxidized in between 50 and 100 days, since microbial CH4 oxidation rates of 0.78 nmol d−1 were measured. Above the pycnocline, methane concentrations decrease to local background concentration of ~10 nmol L−1. Our results suggest that the methane dissolved from gas bubbles is efficiently trapped below the pycnocline and thus limits the methane concentration in surface water and the air–sea exchange during summer stratification. During winter the lateral stratification breaks down and fractions of the bottom water enriched in methane may be vertically mixed and thus be potentially an additional source for atmospheric methane

Methane in the northern Atlantic controlled by microbial oxidation and atmospheric history

During May - August, 1997, the distributions of dissolved methane and CCl3F (CFC11) were measured in the Atlantic between 50° and 60°N. In surface waters throughout the region, methane was observed to be close to equilibrium with the atmospheric mixing ratio, implying that surface ocean methane is tracking its atmospheric history in regions of North Atlantic Deep Water formation. Despite the different atmospheric history and ocean chemistry of CH4 and CFC11, their spatial distribution patterns in the water column are remarkably similar. One-dimensional distributions have been simulated with an advection-diffusion model forced by the atmospheric histories. The results suggest that the similar patterns result from the increasing input of CH4 and CFC11 to newly formed deep waters over time, combined with the effect of horizontal mixing and the oxidation of methane on a 50 year time scale

Ocean currents shape the microbiome of Arctic marine sediments

Prokaryote communities were investigated on the seasonally stratified Alaska Beaufort Shelf (ABS). Water and sediment directly underlying water with origin in the Arctic, Pacific or Atlantic oceans were analyzed by pyrosequencing and length heterogeneity-PCR in conjunction with physicochemical and geographic distance data to determine what features structure ABS microbiomes. Distinct bacterial communities were evident in all water masses. Alphaproteobacteria explained similarity in Arctic surface water and Pacific derived water. Deltaproteobacteria were abundant in Atlantic origin water and drove similarity among samples. Most archaeal sequences in water were related to unclassified marine Euryarchaeota. Sediment communities influenced by Pacific and Atlantic water were distinct from each other and pelagic communities. Firmicutes and Chloroflexi were abundant in sediment, although their distribution varied in Atlantic and Pacific influenced sites. Thermoprotei dominated archaea in Pacific influenced sediments and Methanomicrobia dominated in methane-containing Atlantic influenced sediments. Length heterogeneity-PCR data from this study were analyzed with data from methane-containing sediments in other regions. Pacific influenced ABS sediments clustered with Pacific sites from New Zealand and Chilean coastal margins. Atlantic influenced ABS sediments formed another distinct cluster. Density and salinity were significant structuring features on pelagic communities. Porosity co-varied with benthic community structure across sites and methane did not. This study indicates that the origin of water overlying sediments shapes benthic communities locally and globally and that hydrography exerts greater influence on microbial community structure than the availability of methane