- 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
- 2.2.2.1 Pelagic Communities
- 2.2.2.2 Benthic and Demersal Communities
- 2.2.2.2 Sea-ice Communities
- 2.2.2.4 Mammals and Birds
- 2.2.2.5 Communities of Special Significance
- 2.2.3 Pelagic Realm
- 2.2.3.1 Phytoplankton
- 2.2.3.2 Zooplankton
- 2.2.3.3 Neuston
- 2.2.3.4 Other Pelagic Invertebrates
- 2.2.3.4.1 Krill
- 2.2.3.4.2 Amphipods
- 2.2.3.4.3 Cephalopods
- 2.2.3.4.4 Jellyfish
- 2.2.3.5 Fish
- 2.2.3.5.1 Pelagic Fish
- 2.2.3.5.2 Anadromous Fish
- 2.2.3.5.3 Demersal Fish
- 2.2.3.5.4 Deep-Sea Fish
- 2.2.3.6 Marine Mammals
- 2.2.3.6.1 Bowhead Whale (Balaena mysticetus)
- 2.2.3.6.2 White Whale (Delphinapterus Leucas)
- 2.2.3.6.3 Narwhal (Monodon monoceros)
- 2.2.3.6.4 Ice Seals
- 2.2.3.6.5 Walrus (Odobenus rosmarus)
- 2.2.3.6.6 Orca Whales (Orcinus orca)
- 2.2.3.6.7 Polar Bear (Ursus maritimus)
- 2.2.3.7 Birds
- 2.2.3.7.1 Black-legged kittiwakes (Rissa tridactyla)
- 2.2.3.7.2 Black Guillemots (Cepphus grille)
- 2.2.3.7.3 Thick billed Murres (Uria lomvia)
- 2.2.3.7.4 Northern Fulmar (Fulmarus glacialis)
- 2.2.3.7.5 Common Eider (Somateria mollissima)
- 2.2.3.7.6 Little Auk/Dovekie (Alle alle)
- 2.2.3.7.7 Glaucous gull (Larus glaucescens)
- 2.2.3.7.8 Arctic jaeger (Stercorarius parasiticus)
- 2.2.4 Benthic Realm
- 2.2.4.1 Intertidal Communities
- 2.2.4.2 Shelf and Deepwater Communities
- 2.2.4.3 Mollusca
- 2.2.4.4 Polychaetes
- 2.2.4.5 Amphipods
- 2.2.4.6 Decapod Crustaceans
- 2.2.4.7 Echinoderms
- 2.2.5 Sea-Ice Realm
- 2.2.5.1 Ice Algae
- 2.2.5.2 Sympagic Copepods
- 2.2.5.3 Ice Amphipods
- 2.2.5.4 Pelagic Copepods
- 2.2.5.5 Sympagic Fish
- 2.2.5.6 Mammals
- 2.2.5.7 Birds
- 2.2.6 VECs of Arctic Marine Environments
- 2.2.6.1 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
- 4.2.1.1 Potential Environmental Impact of Untreated Oil
- 4.2.1.2 Conclusions on Natural Attenuation
- 4.2.2 Mechanical Recovery and Containment
- 4.2.2.1 Environmental impacts from Mechanical Recovery and Containment
- 4.2.2.2 Conclusions
- 4.2.3 In-Situ Burning and Chemical Herders
- 4.2.3.1 Potential environmental and human health effects of ISB residues and unburnt oil
- 4.2.3.2 Environmental Impact of Herders
- 4.2.3.3 Conclusions on ISB and Herders
- 4.2.4 Improving Dispersion of Oil
- 4.2.4.1 Impact of Chemically Dispersed Oil
- 4.2.4.2 Conclusions on Chemical Dispersion
- 4.2.4.3 Dispersing Oil using Oil Mineral Aggregates (OMA)
- 4.2.4.4 Environmental Impact of OMA formation
- 4.2.4.5 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
- 5.1.1.1 Transport routes
- 5.1.1.2 Microbial populations in the Arctic Ocean
- 5.1.2 Microbial Adaptation to Arctic Conditions
- 5.1.2.1 Low temperature and microbial adaptions
- 5.1.2.2 Light and microbial phototrophs
- 5.1.2.3 Marine ice and microbial survival and metabolism
- 5.2 Knowledge Status
- 5.2.1 Biodegradation of Oil in Cold Marine Environments
- 5.2.1.1 Types of Crude Oils
- 5.2.1.2 Surface oil spills
- 5.2.1.2.1 Evaporation
- 5.2.1.2.2 Water solubility
- 5.2.1.2.3 Photooxidation
- 5.2.1.2.4 Sedimentation
- 5.2.1.2.5 Water-in-oil emulsification
- 5.2.1.2.6 Natural dispersion
- 5.2.1.2.7 Oil films
- 5.2.1.3 Microbial Oil-Degrading Populations in Cold Water Environments
- 5.2.1.3.1 Indigenous Microorganism Populations
- 5.2.1.3.2 Population Effects on Oil Degradation
- 5.2.1.4 Hydrocarbon biodegradation in cold marine environments
- 5.2.1.4.1 Seawater
- 5.2.1.4.2 Sediments and soils
- 5.2.1.4.3 Sea ice
- 5.2.1.5 Modeling of biodegradation
- 5.2.1.5.1 Biodegradation in oil spill models
- 5.2.1.5.2 Biodegradation modeling and temperature
- 5.2.1.6 Determination of Biodegradation
- 5.2.1.6.1 Analytical methods for oil compound analyses
- 5.2.1.6.2 Experimental apparatus
- 5.2.1.6.3 Biodegradation data processing
- 5.2.1.7 Persistent Oil Compounds
- 5.2.2 Accelerated Biodegradation
- 5.2.2.1 Biostimulation
- 5.2.2.1.1 Shoreline sediments
- 5.2.2.1.2 Seawater
- 5.2.2.1.3 Marine ice
- 5.2.2.2 Bioaugmentation
- 5.2.2.3 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
- 6.1.1.1 Test Exposure
- 6.1.1.2 Test Media Preparation
- 6.1.1.2.1 Water Soluble Fractions (WSF)
- 6.1.1.2.2 Water Accommodated Fractions (WAF, CEWAF)
- 6.1.1.2.3 Oil-in-Water Dispersions (Oil Droplets)
- 6.1.1.2.4 Oil Type/Weathering
- 6.1.1.2.5 Exposure Concentrations
- 6.1.1.2.6 Test Organisms
- 6.1.1.2.7 Test Endpoints and Exposures
- 6.1.1.2.8 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
- 6.2.2.1 Pack ice
- 6.2.2.2 Pelagic
- 6.2.2.3 Benthic
- 6.2.3 Review by Taxa
- 6.2.3.1 Phytoplankton and seaweed
- 6.2.3.2 Mysids
- 6.2.3.3 Copepods
- 6.2.3.4 Amphipods
- 6.2.3.5 Benthic organisms
- 6.2.3.6 Fish
- 6.3 Discussion
- 6.3.1 Petroleum related components
- 6.3.1.1 Crude oil
- 6.3.1.2 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
- 7.2.1.1 Transport and fate / exposure potential
- 7.2.1.2 Oil toxicity evaluations / sensitivity
- 7.2.1.3 Population distributions, stressors, and mortality rates
- 7.2.2 Copepod Population Ecology
- 7.2.2.1 Copepod Growth and Development
- 7.2.2.2 Summary of Arctic and Sub-Arctic Copepod Species
- 7.2.3 Copepod Populations
- 7.2.4 Arctic Fish Population Ecology
- 7.2.4.1 Arctic Fish Species Diversity
- 7.2.4.2 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
- 9.2.3.1 Potential oil spill scenarios
- 9.2.3.2 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
- 9.2.6.1 Assessing response strategy effectiveness and estimating oil fate and transport
- 9.2.6.2 Assessing the potential impacts and resource recovery rates
- 9.2.7 Historical Spills that Used or Informed NEBA Processes
- 9.2.7.1 A. Experimental: Baffin Island tests in northern Canada
- 9.2.7.2 B. Experimental: TROPICS study
- 9.2.7.3 C. Tanker: Braer Spill
- 9.2.7.4 D. Tanker: Sea Empress spill
- 9.2.7.5 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
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8.0 ECOSYSTEM RECOVERY
Executive Summary
Contaminant concentrations, persistence and bioavailability influence the potential for impacts on species living within the different environmental compartments. The interface environments (e.g., ice/water, air/water and shorelines) may be the most critical exposure locations where organisms may come into contact with oil at the highest concentrations, e.g. resulting in increased mortalities due to fouling or smothering. Near term biological effects of oil on pelagic invertebrates and fish is relatively well understood not only in the Arctic but also in non-Arctic environments. Near term and longer term impacts on organisms that live along interfaces (air/water, ice/water, sediment/water and shorelines) is less understood not only in the Arctic but also in non-Arctic environments. In general, the biological attributes that control resilience (or recovery potential) within any faunal group include: size or percentage of population impacted, reproductive potential (progeny produced per unit of time), migratory supplementation potential, and the influence of linked effects to higher trophic levels. Resilience assessment is important for properly assessing recovery. It is recommended to further study the elements that determine resilience of Arctic ecosystem components in order to reduce uncertainties in NEBA decision making.
8.1 Introduction
Recovery of environmental compartments (ECs) and valuable ecosystem components (VECs) can vary from days to decades depending on a wide range of biological, chemical and physical variables. In order to better inform consequence assessments of response actions, evaluation of resiliency, or the ability of VECs or ECs to cleanse themselves from oil contamination and to repopulate communities that have been affected needs to be included in assessments of short-term impacts. Differences in resiliency need to be evaluated; for example, the time for replacement of marine mammals or isolated bird or fish populations impacted from surface or stranded oil could be compared to the time for replacement of pelagic copepods or phytoplankton that are impacted by oil that is physically or chemically dispersed within the water column. Examination of relative resilience potentials suggests that oil spill response actions minimizing impacts on interface environments, long lived or sensitive populations would be preferred. Consequence analyses of response actions need to extend beyond the acute effects and examine chronic impacts that may put populations at risk to determine which action is most effective and results in minimizing the ultimate impact to the broader aquatic environment.
8.2 Knowledge Status
8.2.1 Resilience and Potential for Recovery
Recovery from an oil spill event is controlled by the resilience of an environmental compartment to biological, chemical and physical stressors occurring within each environmental compartment. There is a lack of understanding of the processes that determine resilience for the Arctic as well as all aquatic environments leading to uncertainty in the assessment of recovery. Quantification of recovery is not a standardized assessment making it difficult to document when or whether an environmental compartment has been restored. For the purposes of this section we define recovery in terms of structural and functional components of resident populations. The structure of the compartments is based on quantifiable characteristics of the numbers and types of species, their abundance and biomass (standing crop) or production. The function of the compartments is based on the flow of nutrients through a compartment and the services that those organisms provide to other components. Recovery for each of these structural and functional characteristics within different environmental compartments has different time scales.
Following an oil spill in any environment, different oil spill response (OSR) methods may be used as countermeasures during a spill situation and/or for clean-up in the aftermath. This section focuses on how different OSRs will affect the short and long-term fate of oil in the environment and how this will influence recovery time. Except for mechanical recovery that, under special conditions, can remove a certain percentage of the spilled oil, most OSR actions shift the quantity of oil into different environmental compartments with the objective of reducing the overall consequences of the spill and enhancing recovery. Consequence analyses should include the immediate effects of the spill event and the longer term consequences resulting from differences in the potential for an ecological recovery of affected compartments within the broader ecosystem. Little relevant information exists on ecosystem recovery from oil spills in Arctic environments, but we can draw conclusions and identify uncertainties based on examples from sub-Arctic environments.
Among other factors, ecosystem recovery depends on the amount of oil in various environmental compartments. The physical and chemical properties of the spilled oil influence the availability for microbial processes, bioavailability, and the acute and chronic toxicity of the oil mixture to local fauna. Oil Spill Response (OSR) methods as described in Section 4 are: 1) no response, 2) in-situ burning, 3) use of oil mineral aggregates (OMA), 4) chemical dispersants or herders, and 5) natural recovery. Application of one or several OSR methods alters the amount of oil introduced into various environmental compartments, influencing the total consequences of the spill. Determination of the relative resiliency and the ability of impacted faunal groups to restore after oil exposure is a key component of the assessment but it is less studied and understood.
Table 8-1 explores potential consequences of two decision scenarios (i.e. use of dispersants or non-use) and provides a description of the various attributes of environmental compartments and how they may be affected by these two potential response actions. A question remains: what attributes can be used as indicators of ecosystem recovery, i.e. that the environment has returned to its ‘pre-spill’ condition? In a review by Baker (1999) a few suggestions are put forward. Recovery was defined on the basis of hydrocarbon concentrations, i.e. that hydrocarbon concentrations do not exceed normal background levels for a particular location. The criteria are further refined on the following basis:
- Do not exceed any statutory limits
- Are not lethal to specified organisms
- Do not cause deleterious effects to specified organisms
- Do not cause tainting of food organisms
- Have no detectable impact on the function of an ecosystem
- Do not impair the human use of an area
- Are not visible to the human eye
- Cannot be reduced by enhanced clean-up actions without causing an overall retardation of recovery or damage to the recovering ecosystem
In the context of the present section, criterion 5, "Have no detectable impact on the function of an ecosystem," is the most relevant suggestion and is discussed in more detail in the following paragraphs.
The recovery of an ecosystem following an oil spill is a function not only by the return of contaminant levels to pre-spill state, but more importantly to a dynamic equilibrium state that the ecosystem would have been in had the spill not occurred. It must also be realized that there is no single condition of an ecosystem and that changes to the ecosystem and its environmental compartments occur through time and space. Parker and Maki (2003) define recovery for a biological resource as "occurring when the injured resource reaches a state it would have been if the impact had not occurred". Temporal variations in biological resources affect the assessment of the recovery process; however, the definition is robust to temporal variation because it does not require the resource to return to a specified pre-injured state.
Whether an ecosystem affected by human impact returns to its original condition is difficult to measure. Even if measurable parameters that describe the ecosystem structure and relevant reference sites or historical data are available, often ecosystems do not return to their original state, but rather establishes a new “baseline” over time. At the minimum, this new state might be expected to be at a level of productivity, growth or population dynamics that would sustain the ecosystem trends at rates and states consistent with pre-spill dynamics. With constant and/or fluctuating natural changes, how can we know what an affected area is supposed to be 20-30 years following an accidental oil spill? Changes, human-induced or natural, lead to shifting baselines imposing dynamic trajectories for ecosystem status in reference sites as well as human-impacted sites (Duarte et al. 2009). As such, and in an ecosystem context, ecotoxicology needs to be extended from not only treating toxicity on an individual or organism level, but also to include interactions among a variety of biotic and abiotic factors and components.
Table 8-1. Consequences to environmental compartments resulting from OSR decisions to employ chemical dispersants or physical recovery of surfaced oil
Ecosystem Compartments | Compartment Attributes | Dispersant Applied | Dispersant Not Applied – Physical Recovery | ||||
---|---|---|---|---|---|---|---|
Resiliency | Sensitivity | Exposure Potential | Biodegradation Potential | ||||
Atmosphere |
Mammals and Birds |
Reproductive potential is relatively low |
Sensitive to volatiles |
Behavioral avoidance or attracted to slicks |
Volatilizes and rapid dilution by winds |
Removal of surfaced oil and reduction of volatile exposure |
Release of volatiles until oil concentrations are exhausted |
Surface Water (upper mm) |
Generally less sensitive |
Maximum contaminant concentrations avoided by behavioral responses |
Low potential biodegradation based on lowest surface area to volume ratio exposed to microbial use |
Rapid removal of surfaced oil to subsurface |
< 10% recovery; lowest surface area/volume ratio of oil reduces microbial degradation efficiency; more oil is transported to convergence zone compartments |
||
Neuston, larvae & juveniles |
Reproductive potential is high |
Generally most sensitive stages |
Maximum exposure; unable to avoid fouling or exposure |
||||
Pelagic |
upper 10m (plankton, mid water larval and juvenile fish |
High reproductive potential |
Generally among the more sensitive groups |
Small potential for exposure to high concentrations of petroleum unless treated by dispersants or OMA |
Biodegradation is rapid with the small amount of oil compounds diffused into the water |
High surface area to volume increases microbial biodegradation efficiency; exposure to pelagic organisms increased |
Oil compounds diffuse into the upper layers of water (~1m) but at relatively small rates; less impact on pelagic species; intermediate to large sized droplets with less surface area to volume than dispersed oil → less efficient biodegradation |
> 10m |
High reproductive potential but concentrated abundances are on pycnoclines |
Generally among the more sensitive groups |
Chemically dispersed oil generally remains within the upper 10m of water; > 10m are not expected to have significant effects |
Physical dispersion and diffusion of soluble components do not generally attain these depths at significant effects based concentrations |
|||
Subtidal |
>10m |
Moderate reproductive potential |
Moderate sensitivity but, some very old age classes (deep water corals), unknown sensitivity |
Limited exposure potential for surface oils impacting deep subtidal environments |
Limited biodegradation potential for surfaced oils in deep water subtidal environments |
||
<10m |
Moderate reproductive potential (may be interfered with by oil contact with spawning or feeding aggregates) |
Wider range of sensitivity |
Exposure increases when wind and waves introduce oil to shallower subtidal sediments |
Limited to moderate biodegradation; smaller surface area to volume ratio’s and emulsification |
Nearshore habitats have low potential of impact because of continued dilution and enhanced microbial degradation that occurs from during transport from offshore |
Potential impacts from unrecovered oil contacting shallow subtidal |
|
Intertidal Sands |
Infaunal fish and invertebrates |
Wide range of reproductive potential |
Stranding on intertidal sands re-concentrates surface oil and maximizes exposure |
Surface of stranded oil may undergo further weathering, minor biodegradation |
Unrecovered oil can strand on the surface of beach sands where it can be recovered |
||
Intertidal Cobbles/ Boulders |
Rock epifauna and deep burrowing organisms |
Longer term exposure to residual oil and reintroduction of ‘lingering oil’ to surface compartment |
Poor in storage areas between cobbles and boulders or when weathered and on rock surfaces |
Unrecovered oil can strand on rock surfaces, within cobble / boulders. Long term storage with minimum degradation & potential for continued physical fouling, chemical release and exposure. |
Parker and Maki (2003) define a biological resource in three ways: by taxa, summary statistics, and communities. Recovery should be considered separately for individual taxa assessed, and different taxa may have different timeframes of recovery or resilience to an impact. Summary statistics provides a means for combining taxa, and statistics can be valuable when different taxa vary in time and space. Communities add meaning to the way taxa interact with each other, e.g. diversity indices have been used to define a resource as a community. As such, the availability of reference or historical time series data will enhance the assessment of ecosystem recovery. The ability of an ecosystem to recover and the speed with which it does so, depends therefore on a lot of interconnecting factors and dynamics between species and communities and the environment. Rates and extent of recovery can be estimated through structural and functional relationships, e.g. the productivity or diversity of communities (Lotze et al. 2011). Resilience of functions of an ecosystem is strongly correlated to biodiversity (Levin and Lubchenco 2008), the general stress condition of the systems and to the strength of impact of the perturbation and the reproductive potential of the community that was damaged (Gunderson et al. 2010).
In relation to Arctic marine ecosystems, it is important to note that recovery may be linked to generation time (Lotze et al. 2011) and specific features of the Arctic environment such as a short seasonal window of growth and presence/absence of sea ice. The latter may influence the exposure history following a spill and the possibilities of trapping or removing the oil, which is considered to be a major factor in ecosystem recovery (Chapman and Riddle 2005). Another important note in relation to pressures on the Arctic ecosystems, is the effect of climate change, which apart from opening up possibilities of increased petroleum exploration, has increased the general stress on the system with concerns of acting with synergistic effects (Clarke and Harris 2003; Macdonald et al. 2005).
The BIOS experimental oil spill is one of the few experimental oil spills in the Arctic where changes in biota have been followed. This experimental oil release took place at Cape Hatt, northern Baffin Island in August 1981. Approximately 15 m3 of slightly weathered (8% removal) Lagomedio crude oil was applied to the surface in one bay (bay 11), 15 m3 of dispersed oil (DOR 1:10, Corexit 9527) was released to the surface of another bay (bay 10), and finally 15 m3 was released underwater in a third bay (bay 9). A fourth bay (bay 7) was used as a reference station. Following these crude oil releases, oil concentrations were measured in 1981-1983 and in 1985 and 1987, and effects on Arctic macrobenthos were studied in the acute phase and during a period of 2 years post-spill (infauna: Cross & Thomson (1987), epibenthos: Cross et al. (1987a) and macroalgae: Cross et al. (1987b). No apparent short-term effects of untreated oil were observed on shallow-water infauna, whereas marked acute effects were observed for the dispersed oil treated bay after 24 hours. However, no large-scale mortality of benthic infauna and no significant change in infauna community structure were observed for either treatment. During the recovery phase, the authors claim that most affected infauna organisms recovered, although some persistent changes to bivalves (reproductive effects) and polychaetes (density) were observed even two years after the spills occurred (Cross and Thomson 1987). For epibenthic organisms, narcosis in sea urchins and starfish was observed in the acute phase; however, no major effects on the density of crustaceans were observed over time. Some minor effects were indicated in 2 of 22 of the sites analyzed where possible delayed reproduction and depth distribution of amphipod were suggested (Cross et al.1987a). No effects were observed on macroalgal biomass, number of species and reproductive condition. Only a slight increase in growth for one alga was observed over time, suggested to be a result of reduced herbivore activity (Cross et al. 1987b). Summary observations may best be characterized as the presence of oil with or without dispersants had relatively short-term, localized impacts for this test spill that affected a relatively small area.
Although the Exxon Valdez oil spill (EVOS; 42 million liters of Alaskan North Slope oil were spilled) was not a true Arctic oil spill, it can be used as an example of ecosystem recovery assessment in a sub-Arctic area that represents considerations of impacts over a large area. Numerous papers have dealt with the recovery of specific biological resources in the Prince William Sound (PWS) region since the spill occurred in 1989, and it is beyond the scope of the current literature review to evaluate all information that exists from EVOS. Furthermore, there are still ongoing disagreements between scientists as to what extent the ecosystem has recovered. In a review by Peterson et al. (2003) the general conclusions were that oil persisted in some areas (limited areas compared to the miles of initially oiled shoreline) well beyond a decade in surprising amounts and toxic forms and was sufficiently bioavailable to cause chronic biological exposure and long-term population level impacts. One of the underlying arguments for this was chronic persistence of oil in sediments causing prolonged exposure and health effects to sediment-associated organisms. On the other hand, a review by Harwell and Gentile (2006) presented an assessment based on valued ecosystem components (VEC) and concluded that the PWS ecosystem had effectively recovered from EVOS.
8.3 Future Research Considerations
"Ecosystem recovery" will occur after an oil spill but understanding when an ecosystem has recovered sufficiently has serious gaps of knowledge. There are no papers that deal with ecosystem recovery after an oil spill in the high Arctic and only a few experimental studies in the Arctic that provide limited information to evaluate an oil spill (e.g. BIOS experiments). The studies in Prince William Sound intertidal rocky/cobble substrates suggest that there are ongoing ‘lingering’ effects of the Exxon Valdez spill that occurred more than 20 years ago while other assessment indicate the functional aspects have recovered. These weaknesses highlight the need for a fundamental understanding of ecosystems with a focus on oil toxicity studies at the population and community/ecosystem level. The review of ecosystem recovery in the Arctic described by the authors in this section led to suggestions of further research which can reduce remaining uncertainties. The more generic suggestions compiled from this review are summarized below while recommendations that are important for improving Arctic NEBA are listed separately.
- Ecosystem recovery. New effort needs to focus on appropriate information collected throughout the Arctic and sub-arctic for decades as well as experimental studies to demonstrate rates of recovery under controlled conditions. Expand on the conceptual basis of this section to develop an assessment of the physical and chemical attributes that influence environmental compartment resiliency and ultimately, recovery potential.
- Utilize baseline studies. Environmental baseline studies are conducted at exploration/production sites. Collect, review, coordinate consistency among biological data sets, and archive the validated information on communities of organisms living in different environmental compartments. Establish baseline conditions throughout the Arctic regions anticipated to undergo oil exploration in order to provide the natural range in those characteristics so that the state of recovery can be evaluated.
- Population parameters to be collated or obtained include: overall population estimates for the species abundance, variations in daily mortality rate coefficients, fecundity measures, age structure of populations, frequency of spawning, local broadcast larval distribution, and regions of special biological significance for key species.
- These population characteristics for each species need to be placed into a species resiliency database to provide more accurate estimates of the ability for a species to recover from a stressor.
- The effects of non-dispersed oil on organisms utilizing the sea surface such as seabirds and marine mammals, as well as intertidal and shallow subtidal communities are subjects needing further study. These investigations need to include impacts due to physical fouling and an examination of toxicity caused by various modes of action.
8.3.1 Priority Recommendations for Enhanced NEBA Applications in the Arctic
The recommendations presented below indicate where increased knowledge of oil transport and fate processes would result in reducing existing uncertainties in NEBA assessments. No prioritization has been made to the list; for some of the recommendations, surrogate data may be already available.
- Continue ecosystem-level investigations. Conduct mesocosm experiments that focus on biological interactions of several ecosystem elements instead of single species responses, such as the BIOS experiments.
- Compile data on resiliency metrics of VECs and ECs. Assign semi-quantitative score to species/populations that are considered VECs to Arctic ECs.
- Provide a GIS mapping of seasonal and spatial VEC population use of EC and their resiliency scores.
- Recovery potentials
- Vulnerabilities
- Seasonal weathering/biodegradation and toxicity of OSR residuals
- Introduce recovery metrics. How much change is beyond natural variation? What ecosystem-level attributes should be assessed? Develop exemplary scenarios. Implement full-scale ecosystem consequence analysis.
8.4 Further Information
Authors Dr. Bjørn Henrik Hansen (SINTEF), Dr. Jack Q Word (ENVIRON), Drs. Gina Coelho and James Clark (HDR/EM&A), Dr. Morten Hjorth (COWI), Dr. Lionel Camus (Akvaplan NIVA), Dr. Torgeir Bakke (NIVA)
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