- 0.0 EXECUTIVE SUMMARY
- 0.1 Program Objectives and Participants
- 0.1.1 The Pan-Arctic Region: Highlights of the Literature Review
- 0.1.1.1 Behavior and Fate of Oil in the Arctic
- 0.1.1.2 VECs and Ecotoxicity
- 0.1.2 Role of Ecosystem Consequence Analyses in NEBA Applications for the Arctic
- 0.1.2.1 Arctic Population Resiliency and Potential for Recovery
- 0.2 Priority Recommendations to Enhance NEBA Applications in the Arctic
- 0.2.1 Development of ARCAT Matrices
- 0.2.2 Influence of Oil on Unique Arctic Communities
- 0.2.3 Biodegradation in Unique Communities
- 0.2.4 Modeling of Acute and Chronic Population Effects of Exposure to OSRs
- 0.3 Further Information
- 1.0 THE PHYSICAL ENVIRONMENT
- 1.1 Introduction
- 1.1.1 The Arctic Ocean, Marginal Seas, and Basins
- 1.2 Knowledge Status
- 1.2.1 The Circumpolar Margins
- 1.2.2 Arctic Hydrography
- 1.2.3 Ice And Ice-Edges
- 1.2.4 Seasonality: Productivity and the Carbon Cycle in the Arctic
- 1.3 Future Research Considerations
- 1.3.1 Priority Recommendations to Enhance NEBA Applications in the Arctic
- 1.4 Further Information
- 2.0 ARCTIC ECOSYSTEMS AND VALUABLE RESOURCES
- 2.1 Introduction
- 2.2 Knowledge Status
- 2.2.1 Habitats of the Arctic
- 2.2.2 Arctic Food Webs
- 188.8.131.52 Pelagic Communities
- 184.108.40.206 Benthic and Demersal Communities
- 220.127.116.11 Sea-ice Communities
- 18.104.22.168 Mammals and Birds
- 22.214.171.124 Communities of Special Significance
- 2.2.3 Pelagic Realm
- 126.96.36.199 Phytoplankton
- 188.8.131.52 Zooplankton
- 184.108.40.206 Neuston
- 220.127.116.11 Other Pelagic Invertebrates
- 18.104.22.168.1 Krill
- 22.214.171.124.2 Amphipods
- 126.96.36.199.3 Cephalopods
- 188.8.131.52.4 Jellyfish
- 184.108.40.206 Fish
- 220.127.116.11.1 Pelagic Fish
- 18.104.22.168.2 Anadromous Fish
- 22.214.171.124.3 Demersal Fish
- 126.96.36.199.4 Deep-Sea Fish
- 188.8.131.52 Marine Mammals
- 184.108.40.206.1 Bowhead Whale (Balaena mysticetus)
- 220.127.116.11.2 White Whale (Delphinapterus Leucas)
- 18.104.22.168.3 Narwhal (Monodon monoceros)
- 22.214.171.124.4 Ice Seals
- 126.96.36.199.5 Walrus (Odobenus rosmarus)
- 188.8.131.52.6 Orca Whales (Orcinus orca)
- 184.108.40.206.7 Polar Bear (Ursus maritimus)
- 220.127.116.11 Birds
- 18.104.22.168.1 Black-legged kittiwakes (Rissa tridactyla)
- 22.214.171.124.2 Black Guillemots (Cepphus grille)
- 126.96.36.199.3 Thick billed Murres (Uria lomvia)
- 188.8.131.52.4 Northern Fulmar (Fulmarus glacialis)
- 184.108.40.206.5 Common Eider (Somateria mollissima)
- 220.127.116.11.6 Little Auk/Dovekie (Alle alle)
- 18.104.22.168.7 Glaucous gull (Larus glaucescens)
- 22.214.171.124.8 Arctic jaeger (Stercorarius parasiticus)
- 2.2.4 Benthic Realm
- 126.96.36.199 Intertidal Communities
- 188.8.131.52 Shelf and Deepwater Communities
- 184.108.40.206 Mollusca
- 220.127.116.11 Polychaetes
- 18.104.22.168 Amphipods
- 22.214.171.124 Decapod Crustaceans
- 126.96.36.199 Echinoderms
- 2.2.5 Sea-Ice Realm
- 188.8.131.52 Ice Algae
- 184.108.40.206 Sympagic Copepods
- 220.127.116.11 Ice Amphipods
- 18.104.22.168 Pelagic Copepods
- 22.214.171.124 Sympagic Fish
- 126.96.36.199 Mammals
- 188.8.131.52 Birds
- 2.2.6 VECs of Arctic Marine Environments
- 184.108.40.206 Seasonal Distribution Patterns of Arctic Marine Populations
- 2.3 Future Research Considerations
- 2.3.1 Priority Recommendations to Enhance NEBA Applications in the Arctic
- 2.4 Further Information
- 3.0 THE TRANSPORT AND FATE OF OIL IN THE ARCTIC
- 3.1 Introduction
- 3.2 Knowledge Status
- 3.2.1 Weathering of Oil Spilled in Ice
- 3.2.2 Oil in Ice Interactions
- 3.2.3 Oil on Arctic Shorelines
- 3.2.4 Oil-Sediment Interactions
- 3.3 Future Research Considerations
- 3.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
- 3.4 Further Information
- 4.0 OIL SPILL RESPONSE STRATEGIES
- 4.1 Introduction
- 4.1.1 Environmental Uniqueness of the Arctic Region in Relation to OSR
- 4.2 Knowledge Status - Impact of OSRs
- 4.2.1 Natural Attentuation
- 220.127.116.11 Potential Environmental Impact of Untreated Oil
- 18.104.22.168 Conclusions on Natural Attenuation
- 4.2.2 Mechanical Recovery and Containment
- 22.214.171.124 Environmental impacts from Mechanical Recovery and Containment
- 126.96.36.199 Conclusions
- 4.2.3 In-Situ Burning and Chemical Herders
- 188.8.131.52 Potential environmental and human health effects of ISB residues and unburnt oil
- 184.108.40.206 Environmental Impact of Herders
- 220.127.116.11 Conclusions on ISB and Herders
- 4.2.4 Improving Dispersion of Oil
- 18.104.22.168 Impact of Chemically Dispersed Oil
- 22.214.171.124 Conclusions on Chemical Dispersion
- 126.96.36.199 Dispersing Oil using Oil Mineral Aggregates (OMA)
- 188.8.131.52 Environmental Impact of OMA formation
- 184.108.40.206 Conclusions on OMA
- 4.3 Future Research Considerations
- 4.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
- 4.4 Further Information
- 5.0 BIODEGRADATION
- 5.1 Introduction
- 5.1.1 The Microbiology of the Arctic Oceans
- 220.127.116.11 Transport routes
- 18.104.22.168 Microbial populations in the Arctic Ocean
- 5.1.2 Microbial Adaptation to Arctic Conditions
- 22.214.171.124 Low temperature and microbial adaptions
- 126.96.36.199 Light and microbial phototrophs
- 188.8.131.52 Marine ice and microbial survival and metabolism
- 5.2 Knowledge Status
- 5.2.1 Biodegradation of Oil in Cold Marine Environments
- 184.108.40.206 Types of Crude Oils
- 220.127.116.11 Surface oil spills
- 18.104.22.168.1 Evaporation
- 22.214.171.124.2 Water solubility
- 126.96.36.199.3 Photooxidation
- 188.8.131.52.4 Sedimentation
- 184.108.40.206.5 Water-in-oil emulsification
- 220.127.116.11.6 Natural dispersion
- 18.104.22.168.7 Oil films
- 22.214.171.124 Microbial Oil-Degrading Populations in Cold Water Environments
- 126.96.36.199.1 Indigenous Microorganism Populations
- 188.8.131.52.2 Population Effects on Oil Degradation
- 184.108.40.206 Hydrocarbon biodegradation in cold marine environments
- 220.127.116.11.1 Seawater
- 18.104.22.168.2 Sediments and soils
- 22.214.171.124.3 Sea ice
- 126.96.36.199 Modeling of biodegradation
- 188.8.131.52.1 Biodegradation in oil spill models
- 184.108.40.206.2 Biodegradation modeling and temperature
- 220.127.116.11 Determination of Biodegradation
- 18.104.22.168.1 Analytical methods for oil compound analyses
- 22.214.171.124.2 Experimental apparatus
- 126.96.36.199.3 Biodegradation data processing
- 188.8.131.52 Persistent Oil Compounds
- 5.2.2 Accelerated Biodegradation
- 184.108.40.206 Biostimulation
- 220.127.116.11.1 Shoreline sediments
- 18.104.22.168.2 Seawater
- 22.214.171.124.3 Marine ice
- 126.96.36.199 Bioaugmentation
- 188.8.131.52 Understanding Processes in Accelerated Biodegradation
- 5.3 Future Research Considerations
- 5.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
- 5.4 Further Information
- 6.0 ECOTOXICOLOGY OF OIL AND TREATED OIL IN THE ARCTIC
- 6.1 Introduction
- 6.1.1 General Methods and Relevant Endpoints in Laboratory Testing
- 184.108.40.206 Test Exposure
- 220.127.116.11 Test Media Preparation
- 18.104.22.168.1 Water Soluble Fractions (WSF)
- 22.214.171.124.2 Water Accommodated Fractions (WAF, CEWAF)
- 126.96.36.199.3 Oil-in-Water Dispersions (Oil Droplets)
- 188.8.131.52.4 Oil Type/Weathering
- 184.108.40.206.5 Exposure Concentrations
- 220.127.116.11.6 Test Organisms
- 18.104.22.168.7 Test Endpoints and Exposures
- 22.214.171.124.8 Data Extrapolation and Population Models
- 6.2 Knowledge Status
- 6.2.1 Species represented in the data set
- 6.2.2 Arctic ecosystem compartments in the dataset
- 126.96.36.199 Pack ice
- 188.8.131.52 Pelagic
- 184.108.40.206 Benthic
- 6.2.3 Review by Taxa
- 220.127.116.11 Phytoplankton and seaweed
- 18.104.22.168 Mysids
- 22.214.171.124 Copepods
- 126.96.36.199 Amphipods
- 188.8.131.52 Benthic organisms
- 184.108.40.206 Fish
- 6.3 Discussion
- 6.3.1 Petroleum related components
- 220.127.116.11 Crude oil
- 18.104.22.168 Single PAH
- 6.3.2 Chemically dispersed oil versus physically dispersed oil
- 6.3.3 Are Arctic species more sensitive than temperate species?
- 6.4 Future Research Considerations
- 6.4.1 Priority Recommendations to Enhance NEBA Applications in the Arctic
- 6.5 Further Information
- 7.0 POPULATION EFFECTS MODELING
- 7.1 Introduction
- 7.2 Knowledge Status
- 7.2.1 Parameters Needed to Assess Potential Responses of VECs to Environmental Stressors
- 22.214.171.124 Transport and fate / exposure potential
- 126.96.36.199 Oil toxicity evaluations / sensitivity
- 188.8.131.52 Population distributions, stressors, and mortality rates
- 7.2.2 Copepod Population Ecology
- 184.108.40.206 Copepod Growth and Development
- 220.127.116.11 Summary of Arctic and Sub-Arctic Copepod Species
- 7.2.3 Copepod Populations
- 7.2.4 Arctic Fish Population Ecology
- 18.104.22.168 Arctic Fish Species Diversity
- 22.214.171.124 Representative Fish Species
- 7.2.5 Application of Population Models
- 7.3 Future Research Considerations
- 7.3.1 Priority Recommendations to Enhance NEBA Applications in the Arctic
- 7.4 Further Information
- 8.0 ECOSYSTEM RECOVERY
- 8.1 Introduction
- 8.2 Knowledge Status
- 8.2.1 Resilience and Potential for Recovery
- 8.3 Future Research Considerations
- 8.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
- 8.4 Further Information
- 9.0 NET ENVIRONMENTAL BENEFIT ANALYSES FOR OIL SPILL
- 9.1 Introduction
- 9.2 Knowledge Status
- 9.2.1 Importance of NEBA Development for Arctic Regions
- 9.2.2 Scope and Applicability
- 9.2.3 Information Required to Utilize the NEBA Process
- 126.96.36.199 Potential oil spill scenarios
- 188.8.131.52 Response resources available
- 9.2.4 Ecological Resources at Risk
- 9.2.5 Social and Economic Relevance
- 9.2.6 Historical uses of NEBA and Case Studies
- 184.108.40.206 Assessing response strategy effectiveness and estimating oil fate and transport
- 220.127.116.11 Assessing the potential impacts and resource recovery rates
- 9.2.7 Historical Spills that Used or Informed NEBA Processes
- 18.104.22.168 A. Experimental: Baffin Island tests in northern Canada
- 22.214.171.124 B. Experimental: TROPICS study
- 126.96.36.199 C. Tanker: Braer Spill
- 188.8.131.52 D. Tanker: Sea Empress spill
- 184.108.40.206 E. Well Blowout: Montara spill (also known as the West Atlas Spill)
- 9.2.8 Potential Challenges to Applying NEBA Processes in the Arctic Environment
- 9.3 Future Research Considerations
- 9.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
- 9.4 Further Information
- APPENDIX: USE OF NEDRA IN CONNECTION TO OIL SPILL CONTINGENCY PLANNING IN NORWAY
- 10.0 SUPPORTING REPORTS
Add notes to:
Or add a reference to download later
4.2 Knowledge Status - Impact of OSRs
4.2.1 Natural Attentuation
Several field tests with experimentally released oil have been completed in the Arctic (see SL Ross, 2012 for an overview). However, except for the Baffin Island Oil Spill (BIOS) experiment these tests were devoted to studying the behavior and environmental fate of the oil in icy conditions and not the environmental impact at the spill location or other ECs. Nonetheless, this information helps frame the physical and chemical factors that affect the nature of oil released in an Arctic environment and help to identify the challenges to be encountered in implementation of any type of OSR activity. In fact, this sets the basic expectations for what might occur if natural attenuation were the only response option implemented.
The specific challenge encountered in the Arctic during OSR is the presence of permanent or seasonal ice, which has many consequences (Potter et al. 2012). Ice reduces the sea surface agitation which coupled with the low prevailing temperature, slows down the spreading of the oil slick reducing physical weathering and emulsification that occurs with more active surface water disruption. Ice also limits oil spreading when it is between ice blocks, or when beneath or on top of the ice. This helps keep the oil relatively concentrated reducing the rate of oil weathering. Large quantities of oil can be trapped either in snow, or on or under the ice within spaces found in the unevenness of the ice surface. When ice is forming, oil can be encapsulated in the new ice and thus kept unaltered during the winter season. Oil trapped in ice can then be released to surrounding waters when the ice melts, possibly reappearing as fresh, unweathered oil. Oil has been observed to migrate through the ice, at a rate that is dependent on oil viscosity. Experimental studies have determined that oil components separate within the ice and undergo degradation during the winter in the ice brine channels, as discussed below and in Section 5.
220.127.116.11 Potential Environmental Impact of Untreated Oil
If spilled oil is not recovered or treated, heavier oils may persist on the surface of water or surface of ice and can affect biological communities that are utilizing these interfaces, especially birds or mammals with fur (due to the potential loss of thermal insulation) whereas lighter oils may naturally disperse into the water column. A reduced rate of oil weathering may occur if oil is encapsulated by ice and the oil may not be biologically available until the spring thaw. Another unique attribute of the Arctic is that oil can strand on the shore during the ice-free season, whereas at other times the shoreline may be protected by landfast ice, which prevents oil from coming ashore. Oil stranding on shoreline substrates during the ice free period is subjected to the strong erosional forces of the ice on shoreline substrates during the next ice build-up and ice break-up seasons. Only deeply buried oil that might occur in intertidal cobble fields would be sequestered for extended periods of time (e.g., decades). Therefore in many cases the persistence of oil onshore will be governed by the physical erosional forces that occur in many shorelines which minimize its retention. However, the weathering and recovery processes may be longer (e.g. occupy those area for more than one year) in cases where oil is sequestered in spaces among cobble or boulder fields or where oil may be trapped in isolated nearshore water bodies. The practicalities of staging recovery operations in remote locations are also a consideration.
The effect of oil that is left to natural attenuation on the shoreline depends upon:
- The environmental resources of concern that are present when the oiling occurs and during subsequent seasons when extended oil exposures could be possible.
- The duration certain ECs of shoreline contamination, which may not persist for more than one year in while in others it may be extended for longer periods.
- The resiliency of the populations of various species that were impacted as a result of the spill and treatment methods that were used. The resiliency of these populations and communities of organisms is controlled by fecundity, immigration from unaffected areas, and the diversity of organisms present within the affected habitats.
McAuliffe et al. 1980 reported on the effects of oil on under-ice meiofauna as a part of the BIOS project (McAuliffe et al. 1980). Effects of this experimental spill on ice algae are summarized in a report by SL Ross (2010). In that study, the bottom 10 cm of ice had decreased density of meiofauna, no adverse effects were observed on the ice algal community, and under-ice invertebrates showed no mortality but did drift away from the oil impacted area for days following the spill. All the findings of the BIOS Project are summarized in Li et al. (1992).
A separate study conducted on first-year sea ice off Svalbard showed that there is a migration of bioavailable water soluble components (WSC) from encapsulated oil through the ice to the underlying water (Dickins et al. 2006, Faksness et al. 2012). The estimated toxicity of these dissolved oil components in the ice was calculated using toxic units and the findings indicated that the concentration of WSC in the brine channels might be acutely toxic to the ice fauna. Results from another field study of an experimental release of 7000 L crude oil in the Barents Sea showed low concentrations of dissolved hydrocarbons (maximum concentrations were 4 ppb dissolved hydrocarbons and 32 ppb total hydrocarbons) in subsurface water. Predicted toxicity to the exposed community in the upper layers of the water, expressed as toxic units, was 0.11 or less, indicating that the potential for acute toxicity was low in subsurface bulk water (Faksness et al. 2012). However, the effects of surface oil on organisms using the surface layer, polynyas, ice-edges or adjacent shorelines where oil compounds can be re-concentrated was not assessed.
These studies indicate that there could be effects on the local ice biota if the oil is encapsulated in the ice or trapped underneath the ice. The organisms associated directly with the ice could be exposed to potentially toxic dissolved hydrocarbons over the course of several months, causing potentially toxic oil components to enter the Arctic marine food web. On the other hand, the measured concentrations of dissolved hydrocarbons in the water column, or underneath an untreated oil slick, have been lower than potentially toxic concentrations, perhaps indicating that severe effects to organisms residing in the water column would be negligible. However, this does not take into account the reconcentration processes that occur at interfaces such as the surface of the water, at ice water interfaces, convergence zones and shorelines (refer to Sections 2 and 3).
18.104.22.168 Conclusions on Natural Attenuation
Oil remaining in Arctic habitats without treatment will behave similarly to non-Arctic situations, although chemical processes such as dissolution, volatilization, and biodegradation may occur at a slower rate resulting in increased persistence. In non-ice periods oil spills on the sea surface will remain at the sea surface and be transported in slicks by winds and currents to shorelines, convergence zones, and offshore surface waters. During that process some of the oil will dissolve into the water column or be physically dispersed into the water column as droplets, some will volatilize into the atmosphere, while the majority of the oil may remain on the surface where it will weather, biodegrade, emulsify and accumulate in zones of reconcentration. Subsurface releases of untreated oil will generally rise towards the sea surface but during that transport it may also be rapidly biodegraded based on the increased surface area of oil droplets created by the turbulence of the release. Oil that remains on the sea surface can be stranded on shorelines or concentrate in convergence zones but the oil may also be encapsulated by ice as it forms. In order to facilitate the forecasting of the seasonal dynamics of oil in these compartments, it is important that data are available for NEBA evaluations. This will facilitate the decision making process regarding the most appropriate response option under various conditions.
Such a NEBA process would evaluate the trade-offs of untreated oil containment by ice and treatment efficiency with decreased impact on pelagic environments by dispersant treated oil in non-ice environments. In addition the increased effects of surfaced oil as it is captured and released by formation and melting of ice on seabirds, marine mammals, annual ice fauna and flora should be evaluated. Also the biological significance of overwintered oil and ice must be determined.
Many data that serves as a basis for such evaluations is already available, but improvement of the information base would result in further reduction of uncertainties. Suggested topics for such studies are:
- Measure the biodegradation of oil in ice and trapped within leads or under ice over a winter season. Compare to biodegradation of oil in pelagic waters and surface layers during non-ice periods.
- Does frazzle ice increase biodegradation of oil released from ice by physical grinding and disturbance of oil, creating larger surface area for microbes to degrade the oil?
- 2. Presence of VECs
- Determine avoidance behavior for fish and invertebrate VEC’s associated with oil trapped with ice. Indications are that they will move away from oil.
- Evaluate the use of polynyas or leads by VEC fish, invertebrates, sea birds, and marine mammals and the potential for oil effects in these critical habitats. Compare oil within broken ice fields and open waters as an attraction to seabirds, marine mammals, fish and invertebrates.
- Summarize the same types of information for seabirds, shorebirds, marine mammals.
- Considering the uniqueness of Arctic shorelines influenced by landfast ice, it will be important to understand the dynamic processes controlling the fate and persistence of oil on such shorelines. This will require an assessment of the potential for lingering oil releases and the assessment of the natural decontamination rate resulting from different responses
4.2.2 Mechanical Recovery and Containment
When oil is spilled on the surface of the water or rises from a deep water discharge and then accumulates on the surface it is possible to concentrate the oil by placement of booms in the pathway of the oil transport. As the oil accumulates next to the booms it can be recovered by pumping the captured oil into collection containers. Oil can also be collected e.g. using boats and surface water booms that accumulate the oil as the vessels travel through oil slicks. The success of these processes depends on the encounter rate and efficacy of the mechanical collection techniques and the success of containment or accumulation. Ice can act as a natural boom that allows oil to collect along its edges, within leads, under the ice in pockets, and within polynyas. Ice can also hold the oil for extended periods of time, allowing mechanical recovery to occur over more extended periods of time from its formation to when it begins to melt. Many of the tools used for mechanical recovery are not unique to application in the Arctic but for some adaptations have been made to collect oil mixed with ice (Broje and Keller 2007). The tools used to mechanically recover oil after it is concentrated are described in more detail in the Artic response technology report by SL Ross (2012).
22.214.171.124 Environmental impacts from Mechanical Recovery and Containment
Moving ice, either as ice floes or frazzle ice can interfere with containment and recovery equipment deployment and operations (Potter et al. 2012, EPPR 1998). On the other hand, ice can also slow the spreading of oil on water, keeping a slick thicker during recovery, which increases the efficiency of this type of response activity. Environmental impacts of mechanical recovery are usually considered in terms of emissions of response equipment, noise, and the impacts of the presence of large numbers of personnel. However, it is important to consider that mechanical containment and recovery is a slow, tedious, and challenging response method. Mobilizing and supporting such activities in remote areas adds further inefficiencies and time constraints. Impacts from a containment and recovery response effort are: the impact from oil that is left behind (oil that escapes containment), and impacts from the activities necessary to reclaim or dispose of the recovered oil and associated oily debris.
The impacts considered with natural attenuation are also associated with the residual oil left behind from mechanical recovery. Historically, mechanical recovery in open water spills is often reported as less than 15% of the spill volume and in most cases less than 5%, although specific performance can vary widely from incident to incident (EPPR 1998). Thus, for this report, impacts considered under MNR will also be a large part of any mechanical containment response scenario. Our consideration of the ISB, dispersants and OMA and herder technologies will therefore compare tradeoffs using either mechanical response or naturally attenuation as their baselines.
Mechanical recovery in an Arctic spill situation may have marginal improvements in effectiveness due to the presences of some types of ice conditions, or may have additional inefficiencies brought on by different types of ice. Impacts of residual oil left in the environment due to the low effectiveness of mechanical recovery can also serve as the baseline assessments for evaluating tradeoffs for ISB (with or without herders), chemical and physical dispersants. The areas of proposed work are the same as those included in the natural attenuation section of this report.
4.2.3 In-Situ Burning and Chemical Herders
The in-situ burning (ISB), also referred to as controlled burning, has been the subject of extensive research, development, and testing over the past 30 years in temperate and sub-arctic water (Potter et al. 2012). The basic premise for effective and efficient burns is to collect and/or concentrate the oil slick to a thickness greater than 2 mm and provide an ignition source that can start the burning of surfaced oil. The oil must not be weathered or emulsified to such an extent that there are not enough lower molecular weight compounds (LMW) and available oil to sustain combustion (Fingas and Punt 2000).
ISB can be effective in rapidly removing large quantities of oil from the marine environment. Ideally, about 85 to 95% of the burned oil becomes carbon dioxide and water. The rest, 5 to 15% which is not burned efficiently is converted into particulates (soot) and a few percent is converted into organic compounds and combustion products that remain in the marine environment (Potter et al. 2012). The burn residue from a typical efficient ISB operation is in the order of less than 15% (SL Ross 2010). ISB seems well suited to Arctic conditions and the presence of ice (Photo 4-5). The presence of significant ice formations can keep oil from reaching water (burning of oil on ice) or limit the spreading of the oil on water (burning thick patches of oil on water contained among ice formations).
In-situ burning is an efficient process that removes ~80% of the oil (SL Ross, 2010). However, the residuals of these burns include unburned volatile materials that are released into the air, soot particles that are also mobilized and transported into the air, and the modification of oil compounds into new products or the addition of agents (e.g., herders) and their burn products for release into the air or water. These residues of the burning process (smoke, volatiles, soot particles, additives and unburnt oil) are the potential materials that can pose environmental and human health effects. In addition there is a small risk of causing secondary fires that could threaten human life, property and natural resources; this risk is, however, easily manageable.
Chemical herding agents are products used for thickening an oil slick and concentrating oil on the water surface in order to reverse the effects of spreading. The increase in thickness may facilitate oil combustion during an in-situ burning operation. Several herding agents are listed on the National Contingency Plan registry as approved for use during oil spills, including Thickslick 6535 and Siltech OP-40. A third herder employed by the US Navy (USN herder) has been tested under arctic conditions. The USN herders (65% Span-20 and 35% 2-ethyl 1-butanol) and silicon based herders have been used under Arctic conditions and have been shown to work in cold open water environments as well as in broken ice (Buist and Nedwed 2011).
126.96.36.199 Potential environmental and human health effects of ISB residues and unburnt oil
Generally an efficient burn leaves 5 to 15% of the initial oil as residual or unburnt oil (SL Ross 2010). The residual is mainly composed of high molecular weight (HMW) oil compounds which are similar to those in highly weathered heavy fuel oil. The physical properties of burn residues depend on burn efficiency and type of oil. Factors that determine whether residues float or will sink are: water density, oil chemical properties, thickness of slick, and efficiency of the burn (Buist and Trudel 1995). The residual ash may also settle on the surface of the surrounding ice or sea where it may come into contact with surface dwelling organisms.
Tests have been carried out on the burn residue of Alberta Sweet Mixed Blend which had been used in the Newfoundland Offshore Burn Experiment (NOBE). The water accommodated fraction (WAF) was prepared from the unburnt residue and tested on rainbow trout to assess the 96 h LC50 and on sea urchin for inhibition of fertilization (20 min contact). The maximum total petroleum hydrocarbon (TPH) concentration measured in the test solutions (WAF) was 1.1 mg/L. All samples were not toxic to the tested species (Blenkinsopp et al. 1997). In another study, Daykin et al. (1994) concluded the toxicity of the residue should be lower than that of the initial oil. Other studies showed that the residue had very little or no acute toxicity to key indicator species in salt water and freshwater because an effective burn removes the lightest, most toxic components of crude oil (Blenkinsopp et al. 1997).
In a recent study by Faksness et al. (2010), the semi-volatile organic compounds (SVOCs) in a crude oil prior to and after ISB were analyzed. No volatile analyses were performed, but a removal of approximately 60% of the SVOCs, mainly the decalines and naphthalenes, had occurred during the ISB. Acute toxicity tests with the marine copepod Calanus finmarchicus exposed to the underlying water after ISB indicated no increase in toxicity when compared to WAF generated with unburned weathered oil. These findings were in accordance with the results presented by Daykin et al. (1994) as a part of NOBE. Concerning potential for exposures to the PAHs in burned oil residue, several studies have demonstrated that the concentrations of PAHs in the residue were lower than that in the initial oil.
While the toxicity from uptake of chemical components of the residue does not appear to be a concern to water column organisms, there is possible impact on surface dwelling species (by ingestion and/or direct smothering) and benthic species if the residues were to be stranded onshore or sink onto the sea bed. These risks are however considerably lower than when fresh oil remains on the surface or strands. Concern for such an impact arose during oil spill incidents involving ISB, e.g. the Honan Jade spill in South Korea (1983) and the Haven spill in Italy (1991) where the NRC (2005) reported that the burn residue was typically a semisolid, tar-like layer. The surface oils were burnt, removing the impacts in the surface waters but the burnt residues would sink where they affected the benthos. Such sinking residues consisted of scattered chunks rather than as a continuous mat covering a broad area. While this type of impact on the benthos is very hard to assess it must be considered as part of an overall assessment of potential benefits and impacts of ISB.
Oil combustion produces gas, smoke and soot into the atmosphere. Typically the smoke plume is composed of CO2, steam, soot, CO, SO2, NO2 and VOCs including PAH and BTEX, dioxins and dibenzofuran (Tennyson 1994, Fingas et al. 1993). Despite the fact that VOC concentrations in the plume are usually lower than the accepted threshold value for human health concerns (Buist et al. 1999), responders put an exclusion zone in place to ensure there is limited exposure of downwind communities or wildlife populations to these compounds. Responders are also excluded from the immediate area of the fire and at more lengthy distances downwind of the fire.
In one assessment of the NOBE study Ross et al. (1996) found that burning of 1 Kg of oil produced 40 µg of PAH in the soot/particles while the original oil had 9.5 g/kg of oil. Therefore multiple authors have concluded the ISB residue would have a lower toxicity than the initial oil (Buist et al. 1999, Fraser et al. 1993, Garrett et al. 2000, Li et al. 1992, Lin et al. 2005). The potential effects that would occur with species living at the air/water interface or that break through the surface (e.g. seabirds and marine mammals) were unaddressed by these studies.
The production of smoke during an ISB, and the concentrations of smoke particles at ground or sea levels are usually of most concern to the public as they are highly visible from significant distances and can persist for several miles downwind of a burn. Concerns include human health and wildlife inhalation risks from particulates carried in the smoke plume. Particulate concentrations in the plume are greatest at the burn site, but they decline with increasing distance from the site, primarily through dilution, dispersion, and fallout, but also through washing out by rain and snow (API 2004). The species of greatest concern to atmospheric pollution or fallout of soot and particles will be downstream of the burn and include marine mammals that must breathe at the surface of the sea or species and life stages that live within the very surface of the water.
188.8.131.52 Environmental Impact of Herders
The literature dealing with herders is rather old as these products have not been considered or promoted until very recently. Available data shows that most chemical herding agents are not soluble either in water or in oil (less than 1%; Hayward et al. 1995, MSRC 1993) and are used at low application rates; therefore, acute toxicity of these products to pelagic organisms is generally not considered to be an issue. Additional considerations may be required under special use conditions such as very shallow waters with low flushing rates and organisms abundant in early life stages, but exposures are still likely to be at very low concentrations (Walker et al. 1999, MSRC 1993). The more recent documents deal with the efficiency or operations related to herder use (SL Ross 2010). As with dispersants, the toxicity information is limited to water column organisms and there is little information available on the toxicity of these materials to surface dwelling organisms.
184.108.40.206 Conclusions on ISB and Herders
Most of the available information on ISB deals with the efficiency of the technique and operational guidance. While there is some information regarding monitoring activities to ensure air pollution is not a human health or wildlife exposure issue, information on the environmental impact is more limited. Information on fate and effects studies could be compiled, taking into account the specificity of Arctic environment (species with the possibility of large concentrations of juvenile life stages, especially within the surface microlayer) and additional studies could be conducted to evaluate the persistence of these products and their residues where necessary.
4.2.4 Improving Dispersion of Oil
Chemical dispersants are most effective when applied during or quickly after a spill or sub-sea release event, before dilution, weathering and emulsification of the oil reduces the effectiveness of the dispersants. Modern dispersants are mixtures of solvents consisting of organic carbon chains that are oleophilic and surfactants that are hydrophilic. The combination of oleophilic and hydrophilic components change the surface viscosity of the oils and create small droplets of oil that are released from the surface water and move into the water column or from deep water releases into adjacent deep pelagic environments. These small oil droplets have greatly increased surface area that increases the rate of microbial degradation compared to the oil prior to dispersant application. Dispersant mixtures have been evaluated by numerous organizations to determine their toxicity and efficiency of dispersion under many different environmental conditions. By breaking up the oil and creating micron-sized droplets, chemical dispersion reduces the persistence of a surface slick or the potential for sub-sea discharges to reach the surface and thereby minimizes potential encounters by marine mammals and offshore bird populations. Application of chemical dispersant to sub-surface and to surface oil slicks reduces the amount of oil that becomes stranded on the shoreline and prevents oil from transforming into weathered oil-in-water emulsions that are resistant to further biodegradation (Lewis and Daling 2001).
However, dispersing oil into the water column from surface slicks or deep water releases is most effective when the oil is fresh and unweathered. Mitigating damage to the shoreline and to organisms that may encounter surface slicks means exposing the near surface and shallow or deep pelagic communities to elevated concentrations of dispersed oil for short periods of time.
The literature reviewed focused on dispersant applied at the sea surface and it contains information on the toxicity of oil chemically dispersed into the water column and effects on those marine organisms from laboratory studies. Information on the behavior of dispersants applied below the upper surface layer during blow-out scenarios were sparse during this review period. However, it is expected that post-spill studies of the recent Macondo well blow-out and explosion that occurred in 2010 in the Gulf of Mexico will contribute greatly to our knowledge of subsea application of dispersants as well as natural dissolution and biodegradation processes that can occur in the deep ocean environment and at very cold temperatures that are similar to arctic temperatures.
There are limited holistic assessments that combine the toxicity of chemically dispersed oil data with information on specific assessments on toxic impacts associated with Arctic communities or the comparative damage resulting if oil persists on the surface or comes ashore. Therefore, the rationale for application of chemical dispersants should be based on the comparison of the possible extent and duration of impacts to the organisms living in the water column (e.g. fish, shellfish, plankton, etc.) resulting from the use of dispersants, and the extent and duration of potential damage which would result if dispersants were not used, i.e. from a persistent surface slick (e.g. effects to birds, mammals, and fish and invertebrates that live in the very surface of the water) and from the stranding of the weathered oil on the shoreline (e.g. effects to coastal shoreline species and benthic organisms). This type of information must be factored into the tradeoffs associated with Arctic dispersant use, and is considered in the section “Monitoring Natural Recovery (no active response)”.
220.127.116.11 Impact of Chemically Dispersed Oil
Most toxicity studies evaluate the impact of increasing the exposure of pelagic organisms to oil as a result of dispersing the material into the water column. Considering the toxicity toward water column organisms, it is recognized that the observed toxicity effects from chemically dispersed oil is due to the effects of the increased quantity of dispersed oil into the water and are not caused by the dispersant itself, as modern dispersant formulations are much less toxic than oils (Hemmer et al. 2011).
In assessing dispersed oil toxicity, determinants of adverse effects for a given species are exposure concentration and duration of exposure (see also a more detailed review of peer-reviewed literature presented in Section 6, Ecotoxicology of Oil and Treated Oil). A review of field studies found that small-scale field tests have demonstrated that the concentration of dispersant in water falls to less than 1 mg/L within hours (NRC 2005). The available data suggest that in general, maximum dispersed oil concentrations after a spill are less than 50 mg/L immediately after dispersion into the upper water column (top 3 m) and that dispersed oil concentrations dilute rapidly, dropping to 1 to 2 mg/L in less than 2 h throughout the water column (Cormack and Nichols 1977, Daling and Indrebo 1996, McAuliffe et al.1980). These low concentrations are generally below estimated toxicity threshold concentrations derived from exposure experiments for most common water column organisms (McFarlin et al. 2011, Gardiner et al. 2013).
The BIOS experiment conducted in sub-Arctic nearshore areas in the 1970s studied oil dispersion impact on nearshore environments and concluded that the results offer no compelling ecological reasons to prohibit the use of chemical dispersants on oil slicks in nearshore areas (Potter et al. 2012). Secondly, the results provide no strong ecological reasons to undertake an intrusive effort to cleanup stranded oil (on certain shoreline types).
During an experimental oil spill in the Barents Sea in 2009, 2000 L of crude oil were dispersed six hours after release (Potter et al. 2012). Two hours later, measurements of oil in water were performed at depths of 1, 2 and 3 m. The maximum concentration of oil in water was measured to 5.5 ppm (at 2 m depth) with an oil droplet size smaller than 10 µm, 30 minutes after mixing energy was added by the ship thrusters. The monitoring indicated background concentrations were restored shortly after these measurements, as the plume had most likely drifted and diluted with the currents (Merlin and Le Floch 2012). After the Sea Empress incident, a major spill in nearshore waters at the port of Milford Haven, UK, dispersed oil concentrations were monitored and quantified in the field. Results showed 10 ppm dispersed oil immediately after the dispersant application, decreasing to 1 ppm 2 days after, 0.5 ppm 1 week after and 2 ppb 1 month after (SEEEC 1998).
Such a decrease can be modeled with the following relationship:
Where C equals oil concentration at time (t in hours);
C0 is the initial concentration;
e-1.35 represents an exponential decline in oil concentration
Application of the equation yields a half-life of 12 h for the dispersed oil concentrations [every 12 hours the concentration is divided by 2 (Merlin and Le Floch 2012)]. This reflects a dilution rate for a sustained spill response implemented over several days in a deep, but nearshore environment. In more recent toxicology studies carried out in several laboratories in North America (Aurand and Coelho 2005), the exposure duration was modeled after a single dispersant application to offshore, open water habitats establishing a half-life of 4 hours. These representations of ‘spiked’ exposures are more environmentally realistic (closer to real field conditions) than standard laboratory ‘constant’ exposures, and result in a reduced level of effects (Gardiner et al. 2013).
The effect and toxicity of a water soluble fraction (WSF) versus chemically dispersed oil was studied by using realistic exposure concentrations based on the WSF concentrations monitored during an offshore field experiment (i.e. initial TPAH concentration of less than 7 ppb; NRC 2005). The Arctic amphipod Gammarus setosus was used as test species in a continuous flow experiment. Body burden measurements showed higher level of PAHs in the gammarids exposed to oil and dispersant for 12 days than in those exposed to oil alone, consistent with the higher concentrations of oil that would be present when dispersant are used. Several biomarkers were monitored, and gammarids exposed to oil and dispersant also showed moderate signals of exposure after recovery in clean seawater.
In a recent study on adult and juvenile fish and bivalve species conducted at elevated concentrations (up to 70 mg/L), the observed effects were sublethal and temporary. After 2 weeks, sublethal bioindicators did not show any differences between animals exposed to the chemically dispersed oil and mechanically dispersed oil (Merlin and LeFloch 2012). This demonstrates that exposure to chemically dispersed oil is not more toxic than the physically dispersed oil. However, the same research team reported that fish kept in a natural environment after exposure did show residual responses (persistent) in terms of growth (Merlin and LeFloch 2012). In conjunction with the previous study, experiments conducted with herring embryos in a wave tank showed abnormalities after constant exposure to elevated concentrations (to 10 ppm), but no effect when a more realistic and rapid dilution exposure regime was generated (McIntosh et al. 2010).
Dispersant toxicity research has been conducted recently on specific Arctic species of concern as part of a laboratory toxicity testing program conducted in Barrow, Alaska. It was found that Arctic species that were tested have similar or greater tolerance to representative concentrations of dispersed oil compared to the numerous temperate species that have been tested (Word and Gardiner in prep.). Also, the acute toxicity of exposures to dispersant alone only occurs at concentrations that are greater than concentrations proposed for application of dispersant products in OSR (McFarlin et al. 2011; Gardiner et al. 2013). For most species that have been tested, dispersed-oil acute toxicity thresholds are on the order of 1 mg/L based on laboratory tests that expose test organisms for periods of 2 to 4 days. Water column concentrations above toxicity thresholds in an actual spill are limited to the top few meters and exposures at potentially toxic concentrations are limited in duration due to rapid dilution kinetics.
18.104.22.168 Conclusions on Chemical Dispersion
The available body of laboratory data, experimental field studies and monitoring following actual spills shows that dispersed oil may potentially cause environmental impacts but these will be limited to the organisms in the immediate vicinity of dispersed oil plume and in cases when the rate of dilution of the dispersed oil plume is slow. This would be the case for sensitive areas with limited water exchange,e.g. close to the shore. Even in such cases, these impacts would generally be limited to non-mobile organisms. For example, monitoring following dispersant use at major oil spill incidents over the past 40 years has never reported significant losses of mature fish populations at sea following dispersant applications.
Laboratory and field research as well as monitoring following actual incidents assessing the impact of use of dispersants in OSR, demonstrate that:
- The toxicity of oil/dispersant mixtures is related to the oil in the mixture and not the dispersant.
- The toxicity of the oil is directly related to the amount of oil that organisms are exposed to. That is, when dispersants are applied to oil the increase in response of pelagic organisms is directly related to the exposure concentration and duration of exposure to the oil.
- The toxicity of dispersed oil is relatively low and often not observable in real environment as long as there is no restriction to the rapid dilution process of the plume of dispersed oil (e.g. open-ocean).
- There is no evidence that Arctic species are more or less sensitive than other temperate climate species that have been tested with dispersed oil.
22.214.171.124 Dispersing Oil using Oil Mineral Aggregates (OMA)
The use of fine mineral particle (such as clay minerals) is an alternative response method to dispersant used to break up an oil slick into small droplets and stabilize the oil dispersion in the water column. When applied to physically dispersed oil, oil droplets aggregate readily with suspended particulate matter (SPM) such as clay minerals and organic matter to form [oil-SPM] aggregates called oil mineral aggregates (OMA; Le Floch et al. 2002). It is important to distinguish the use of OMA from sinking agents. Rather than bind to bulk oil as dense sediment and cause the oil droplets to sink, OMA will cause the oil to be suspended in the water as micron-sized droplets associated with a complex of mineral material in much the same result as chemical dispersants generate micron sized droplets (Khelifa 2005, Khelifa et al. 2005). The simplest form of OMA consists of an oil droplet coated with micrometer-sized solid mineral particles that prevent the droplets from sticking to each other and reforming a slick. When OMA forms, the dense mineral fines (small but 2.5 to 3.5 times denser than most oils) adhering to the oil droplets will reduce the overall buoyancy of the droplets, retarding their rise to the surface but keeping them somewhat buoyant so they do not sink. This promotes oil droplet dispersion throughout the water column to low concentrations, and ultimately enhancing their biodegradation by natural bacteria (Lee et al. 2011).
Positive lab and basin tests of the concept led to a field test in 2008 (Lee et al. 2011). The field test was designed to evaluate the concept of using an icebreaker’s propeller and application of mineral chalk fines with seawater to create OMA. Visual observations confirmed that the oil stayed physically dispersed in the upper water column and did not resurface (Potter et al. 2012). Attempts were made to combine chemical dispersant use with fine mineral application. The dispersant was added to promote the dispersion of micron-sized droplets into the water column while the addition of fines attempted to stabilize this dispersion. The result was not especially convincing, as dispersant presence seemed to inhibit the formation of OMA complex with the oil droplets.
Preventing the re-surfacing of the droplets under the adjacent ice in the Arctic would be a significant environmental benefit since OMA also enhances natural biodegradation of spilled oil. The application of fine minerals seems well adapted to ice infested conditions as the presence of ice reduces the sea surface agitation; chemically dispersed oil may tend to resurface over prolonged time periods if not stabilized by OMA formation. It is also beneficial that the types of fine minerals needed for OMA dispersion are those that are commonly stockpiled in oil exploration facilities as drilling mud components; consequently, a source would be readily available in the event of a spill.
126.96.36.199 Environmental Impact of OMA formation
Most of the studies on this topic were devoted to the mechanism and efficiency of the technique to optimize the application conditions; very few considered the environmental impact of the use of OMA. A lab study dealing with the use of dispersant in estuaries assessed the toxicity of dispersed oil with presence of Montmorillonite clay (Merlin and Le Floch 2012). It was shown that the presence of this fine grained material reduced the observed impact on biota exposed to the dispersed oil plume to the level of impact commonly seen from oil that is mechanically dispersed (without chemical dispersant addition). To date, sparse information has been identified on the environmental impacts and relative toxicity of OMA in the Arctic.
Laboratory and field research as well as monitoring following actual incidents assessing the impact of use of OMA in OSR, demonstrate whether:
- The toxicity of oil/OMA mixtures is altered or if the oil in the mixture is the predominant cause of any toxicity observed with OMA use.
- The association of oil and OMA may alter the toxicity of the oil by decreasing bioavailability due to the adsorptive process that occurs to the OMA.
188.8.131.52 Conclusions on OMA
The environmental advantages of using OMA to stabilize oil dispersion in the upper water column are similar to those expected from the use of chemical dispersant. Mineral fines are nontoxic to marine life. The main impact expected from addition of the mineral fines could be a temporary increase of the sea turbidity which should be similar to the level of turbidity promoted by chemical dispersion. Other mechanisms of impact would be similar to the environmental/biological impacts discussed with chemically dispersed oil. The description of the flocculation of fines to the outer surface of small oil droplets leads to the following questions prior to its acceptance as an OSR option for the Arctic.
- What is the optimum rate of OMA application to oil to maximize its benefits (OMA may need a 1:1 ratio with oil to provide its benefits.
- Does OMA surface coating of oil droplets reduce potential microbial degradation or use of the oil droplets?
- Does OMA surface coating of oil droplets reduce the potential toxicity of the droplets or decrease the solubility and exposure of the more soluble/toxic components of the oil?
- Are OMA coated oil droplets available to suspension feeding organisms in an unweathered, potentially more toxic form?
- The remaining questions regarding the long term environmental fate of the OMA aggregates are: do they tend to sink progressively with time? What is the impact of settled OMA to the exposed area of bottom resources that could be large but at very diffuse concentrations? Does the mineral separate from the oil droplet? What is the impact of OMA or separated mineral exposures to dilute inorganic particulate matter and would it be any different than that endured from settling of ocean particulate matter?