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DIRECTORATE GENERAL FOR INTERNAL POLICIES POLICY DEPARTMENT B: STRUCTURAL AND COHESION POLICIES FISHERIES SEALS AND FISH STOCKS IN THE NORTH-EAST ATLANTIC NOTE Abstract: Industrial and offshore fisheries using active gear have minor or insignificant interactions with seals, whereas some coastal fisheries based on passive gear can experience severe losses in catches and damages to gear. Seals also have impacts on fish farms, which can be protected by a combination of mitigation measures such as hunting, predator nets and acoustic deterrents. Seals spread a parasitic worm, which is seldom a problem in oceanic systems, but may be locally abundant close to main seal colonies. IP/B/PECH/NT/2010-118 October 2010 PE 438.615 EN This document was requested by the European Parliament's Committee on Fisheries. AUTHOR Tero HÄRKÖNEN Swedish Museum of Natural History, Department of Contaminant Research, Stockholm RESPONSIBLE ADMINISTRATOR Irina POPESCU Policy Department Structural and Cohesion Policies European Parliament E-mail: [email protected] EDITORIAL ASSISTANTS: Virginija KELMELYTE Lea POLJANCIC LINGUISTIC VERSIONS Original: EN ABOUT THE EDITOR To contact the Policy Department or to subscribe to its monthly newsletter please write to: [email protected] Manuscript completed in October 2010. Brussels, © European Parliament, 2010. This document is available on the Internet at: http://www.europarl.europa.eu/studies DISCLAIMER The opinions expressed in this document are the sole responsibility of the author and do not necessarily represent the official position of the European Parliament. Reproduction and translation for non-commercial purposes are authorized, provided the source is acknowledged and the publisher is given prior notice and sent a copy. Seals and fish stocks in the North-East Atlantic CONTENTS LIST OF ABBREVIATIONS 4 LIST OF FIGURES 5 LIST OF TABLES 5 General information 9 1. Effects of seals on the dynamics of fish stocks 1.1. Impacts of seals in oceanic ecosystems 11 11 1.1.1. Insignificant or unlikely impacts on sizes of fish stocks in oceanic ecosystems 12 1.1.2. 14 Potential or likely impacts on fish stocks in oceanic ecosystems 1.2. Impacts on fish stocks in coastal and estuarine environments 15 2. Impacts on catches and fishing gear 17 2.1. Impacts in oceanic ecosystems 18 2.2. Impacts in coastal and estuarine environments 18 2.2.1. Angling 18 2.2.2. Encircling gill nets 18 2.2.3. Set gillnets 19 2.2.4. Bag nets and fish traps 19 2.3. Mitigation measures 20 2.3.1. Protective hunting 20 2.3.2. Modification of fishing gear 20 2.3.3. Acoustic deterrants 21 3. Spread of parasites where seals act as final hosts 23 3.1. Seal worm in fish in oceanic ecosystems 25 3.2. Seal worm in coastal ecosystems 26 3.3. Seal worm in estuarine and brackish water ecosystems 26 4. Aquaculture 27 4.1. Interactions with seals and mitigation measures 28 4.2. Considerations 28 References 31 3 Policy Department B: Structural and Cohesion Policies LIST OF ABBREVIATIONS ADD Acoustic Deterrent Device AHD Acoustic Harassment Device HELCOM The Helsinki Commission ICES International Council for Exploration of the Sea OSPAR Convention for the Protection of the Marine Environment of the North-East Atlantic 4 Seals and fish stocks in the North-East Atlantic LIST OF FIGURES Figure 1 Interactions between seals and fisheries are evaluated in OSPAR areas I and II and the Baltic Sea 8 Figure 2 Harbour seals tagged with satellite transmitters in the Danish Wadden Sea can forage over extensive areas, but also in the vicinity of their haul-out sites 15 Figure 3 Fisheries using passive gear operating vessels <12m contribute by 13%, and larger vessels by 2% to the economic value of the Swedish fisheries 18 Figure 4 Encircling gillnets have been used as a main fishing method for thousands of years 19 Figure 5 A grey seal raiding a herring gillnet in the Baltic 20 Figure 6 Whale worm (Anisakis simplex) in the it is also common in herring and cod. whale worm, toothed whales such as indicated to be more important for the 24 abdominal cavity of a mackerel, but Although seals act as final hosts for harbour porpoises and dolphins are occurrence of whale worm in fish Figure 7 Location of cod samples taken for analyses of whale worm and seal worm 25 LIST OF TABLES Table 1 Abundance (counts) of harbour seals in the North-East Atlantic 13 Table 2 Abundance of grey seals in the North-East Atlantic. *Numbers of pups x 4.5 14 Table 3 Frequency (%) and mean numbers (brackets) of whale worm (Anisakis simplex) and seal worm (Pseudoterranova decipiens) in east Atlantic cod 26 5 Policy Department B: Structural and Cohesion Policies Table 4 Production of farmed salmon and trout in the North-East Atlantic. Losses to seals and mitigation methods 27 Table 5 Effectiveness of anti-predator controls in Scottish fish farms 28 6 Seals and fish stocks in the North-East Atlantic EXECUTIVE SUMMARY Background Man and seals have a long and turbulent common history in the North-East Atlantic. A thousand years ago the grey seal was the dominating seal species in the coastal regions of the European continent including the Baltic, whereas harbour seals mainly occurred in tidal areas at the English east coast and the Norwegian fiords (Härkönen et al., 2007). Since grey seal pups need to be nursed on land during their first two to three weeks, they are very vulnerable to hunting in areas where man has access to their breeding grounds. Decreasing numbers of grey seals were noted along the Dutch coasts already in the early Middle Ages, after which they became extirpated from the continental North Sea coasts in the late Middle Ages (Härkönen et al., 2007). Grey seals were here replaced by harbour seals since their pups can swim directly after being born, and are thus less vulnerable to hunting. A similar change occurred later in the Skagerrak, where grey seals were extirpated in the 1750s and replaced by harbour seals (Härkönen et al., 2005). Most countries in the North-East Atlantic introduced bounty systems in the late 19th century and the early 20th century with the explicit objective to exterminate the seals (Harding and Härkönen, 1999). Seal numbers were substantially reduced around the British Isles, the North Sea coast and the Baltic Sea in the 1920s and 1930s (Harding and Härkönen, 1999, Härkönen et al., 2007). In this process grey seals were extirpated from the Kattegat and the Southern Baltic coast, and populations of harbour seals decreased typically by 90-95% Härkönen et al., 2007). Some protection for British seals was introduced in the 1930s, but hunting wasn’t prohibited until the 1960’s in the North Sea area and the late 1970s and 1980s in the Baltic. After protective measures were taken, the very depleted seal populations started to recover and most seal populations have been growing exponentially until very recently, where North Sea populations in Scotland have showed slow or negative growth rates during the last decade. Seal populations have been regulated by hunting in Iceland, the Faroes and Norway during the 20th century, which still is the current management strategy in those countries. The growing seal populations have led to increasing interactions with especially the coastal small scale fisheries, where fishing techniques developed under periods with very low abundances of seals are vulnerable to different types of damages. Aim The aim of the present note is to provide a comprehensive qualitative analysis of interactions between seals and fisheries in the North-East Atlantic, which is defined as the OSPAR areas I and II and the Baltic Sea (Figure 1). 7 Policy Department B: Structural and Cohesion Policies The approach is focused on compiling and evaluating available information from published papers, published and unpublished reports and databases. Impacts of seals on fisheries are studied by categorizing effects on: Figure 1: Interactions between seals and fisheries are evaluated in OSPAR areas I and II and the Baltic Sea Source: ICES (2004) Size and dynamics of fish stocks Seal predation on catches and impacts on fishing gear Spread of parasites where seals act as final hosts Aquaculture 8 Seals and fish stocks in the North-East Atlantic GENERAL INFORMATION KEY FINDINGS The consumption of seals on commercially valuable fish stocks is typically less than 1 % of catches taken by fisheries or spawning stock sizes in offshore areas. Effects of seals on sizes of fish populations are therefore insignificant in oceanic systems. Local high densities of seals in coastal areas can under some circumstances have measurable effects on catches of salmonids, although this only has been shown in few cases. Approximately 90% of all fish are taken by active gear off the coasts of the NorthEast Atlantic and these fisheries are to a minor or insignificant extent affected by seal predation on catches and damages on gear. Static gear such as set gillnets in coastal areas and the Baltic are very vulnerable to impacts from seals, and catch losses may vary between 20% and more than 50% in cod gillnets and herring gillnets. Gillnets are difficult to protect against seal damages since seals get accustomed to acoustic deterrents. Fish traps, bagnets and fykenets are also vulnerable to impacts from seals, which have caused substantial damages to fisheries in the Baltic. Modifications of fish traps have successfully reduced damages both to catches and gear. Seal worms are found in fillets of cod, hake and other cod fishes. The prevalence of seal worms depends on the proximity to main seal colonies, availability of intermediate hosts, and fish species which accumulate worm larvae. Offshore fisheries are much less affected by seal worms as compared with coastal fisheries. Seal worms are often confused with whale worms, which occur in greater abundances and also in oceanic environments. Whale worms are predominantly spread by toothed whales and minke whales. Fish farms are affected by seals but losses seldom exceed 1% in Norway, Iceland and the Faroes. Losses in Scotland range between 1-5% depending on location and which protective measures are taken. Allocation of farms far away from main seal colonies reduces losses. Shooting of seals is an effective mitigation method, but hunting pressure needs to be intense enough to deplete local seal populations. Harbour seal populations in Iceland, Norway and Scotland are decreasing rapidly, and the Faroese population is extinct. Reductions of seal populations are in conflict with the EU-Habitats Directive and the 2006 HELCOM seal recommendation, which state the long-term objectives for management of marine mammals are to attain “natural abundances and distributions”. 9 Policy Department B: Structural and Cohesion Policies One often disregarded aspect in discussions on seal fisheries interactions is that fisheries using active gear offshore, accounting for approximately 90% of all landings, have minor or insignificant impacts from seals (Kashner et al., 2006). Consequently, interactions with seals do not constitute a general problem for fisheries, but affect segments of the industry that account for about 10% of all landings in the North-Eastern Atlantic. More specifically, small scale coastal fisheries using passive gear are in many cases affected by seals damaging catches and gear. It is also the small scale fisheries in some regions with large seal colonies that to a greater extent than the offshore fisheries are affected by seal worms. Recent advances in modifying fish traps set for salmon, whitefish and cod have significantly reduced damages to both catches and gear, whereas problems with gillnets remain since acoustic deterrents are inefficient and also difficult to deploy in practice. 10 Seals and fish stocks in the North-East Atlantic 1. EFFECTS STOCKS OF SEALS ON THE DYNAMICS OF FISH KEY FINDINGS The ecological complexity, multi-species interactions and a high degree of interannual variation make it difficult to assess impacts of seals on the species they prey upon. However: Seals are unlikely to have significant impacts on sizes of fish stocks in complex oceanic ecosystems. Seal predation on commercially important fish species is insignificant for the offshore fisheries. In ecosystems such as the Barents Sea, where seals are very abundant (millions), they can have measurable impacts on the abundances of their prey species. Although seals generally have minor or insignificant impacts on the size of fish stocks in coastal and estuarine ecosystems, seal predation on salmonids in some river mouths reduce catches in the fishery. Studies attempting to evaluate effects of seals on the dynamics of fish stocks face the challenge to model species interactions at the ecosystem level. Multispecies models aiming at predicting outcomes of different scenarios encounter severe problems since each of the included parameters contain a measurement error (variance). Adding the variances for all parameters will lead to model outputs where the predictive values are close to zero. This is also reflected in the ongoing debate whether or not specific ecosystems are controlled “top-down” or “bottom up” (e.g. Frederiksen et al., 2006; Kashner et al., 2006; Baum et al., 2009). However, such models can be useful for studying specific features such as interactions between parameters under specific scenarios where a number of other parameters are kept constant (Pinnegar et al., 2008). A more constructive approach is to evaluate potential impacts by studying how large a proportion of the total mortality of commercially important fish species is caused by seals, or to relate the consumption of seals to the size of the fishery. However, sizes of commercial catches are not directly comparable with removals caused by seals, since fisheries and seals in most cases target different size classes of fish. 1.1. Impacts of seals in oceanic ecosystems The role of top predators such as seals for the dynamics of fish stocks is very complex since seals prey upon a large variety of fish species and also coexist with a number of other predators such as whales, piscivorous sea birds, predatory fish, and invertebrate predators. This top-down effect caused by single predator species appears to be weak in most oceanic ecosystems (Kaschner et al., 2006; Baum et al., 2009), but may be important in specific cases, where a top predator is very abundant (Haug et al., 1995). Seals may also have measurable effects on local abundances of fish in some coastal and estuarine environments (Fjalling et al., 1995; Kauppinen et al., 2005; Butler et al., 2006). These situations will be evaluated separately in the following. 11 Policy Department B: Structural and Cohesion Policies 1.1.1. Insignificant or unlikely impacts on sizes of fish stocks in oceanic ecosystems The decreasing numbers of grey seals (5,000) and harbour seals (8,000) in Iceland (Hauksson and Bogason, 1997; ICES, 2004; Tables 1 and 2) are unlikely to have significant effects on the fish stocks they prey upon. The summer diet of grey seals in Icelandic waters is constituted of cod (24%), sandeel (23 %), catfish (15%), lumpsucker (7%), whereas other species made up less than 1% of the diet (Olafsdottir and Hauksson, 1997). Both grey seals and harbour seals occur along the Norwegian coast, but the about 6,000 grey seals and 12,000 harbour seals (Tables 1 and 2) are too few to have measurable effects in off-shore areas. Total fish consumption by seals in Norway is approximately 30,000 tonnes as compared with 2,5 million tonnes caught by the fisheries. Seal predation on species targeted by the fisheries is less than 1% of of catches. A similar situation in found in Faroese waters, where the less than 500 grey seals, preying predominantly on sandeels, catfish and cod (Mikkelsen et al., 2002), are too few to have significant impacts on fish stocks. Catches in the Faroese fishery vary around 500,000 tonnes. Increasing numbers of harbour seals, which are the most abundant seal species in the Kattegat and the Skagerrak, have led to concerns from the fisheries about possible impacts on commercially important fish stocks. However, since harbour seals are generalists feeding on a large variety of fish species, where the main prey size is beneath 30cm, the competition with fisheries in oceanic ecosystems is insignificant (Härkönen, 1987; Härkönen and Heide-Jörgensen, 1991; Hansen and Harding, 2006). Potential landings of cod would not be affected even if all harbour seals were removed from the ecosystem, since their predation on cod is minor compared with the mortality caused by the fisheries (Hansen and Harding, 2006). Grey seals are the most abundant seal species around the British Isles, and the North Sea stock is close to 100,000 animals (Anon., 2008, Table 2). They range over large areas in the western North Sea (McConnell et al., 1999), where different species of sandeels constitute the most important prey (Prime and Hammond, 1990). Sandeels are also targeted by industrial fisheries, but a combination of factors such as grey seals also preying upon other main predators of sandeels, and the occurrence of other highly abundant predatory fish species such as mackerel and whiting, make direct competition with the fisheries unlikely (Prime and Hammond, 1990; Furness, 2002). Grey seals in the North Sea also prey upon many other commercially important fish species (Hammond and Grellier, 2005). Comparing consumptions of grey seals in 1985 and 2002, it was found that the estimated prey consumption was less than 1% of spawning stock sizes of all species targeted by fisheries. As a consequence of increasing grey seal populations and decreasing fish stocks the prey consumption of grey seals was higher in 2002, but exceeded 1% of stock sizes only for cod (3.7%), sandeel (2.7%) and plaice (1.5%). Consequently, grey seal predation on commercially important fish species is insignificant or minor in the North Sea area. There is not enough data and information to assess potential impacts of seals on fisheries in the Wadden Sea. 12 Seals and fish stocks in the North-East Atlantic Table 1: Abundance (counts) of harbour seals in the North-East Atlantic LOCATION COUNT YEAR CHANGE OVER PAST 5 YEARS Svalbard 1000 2005 Unknown Iceland 8023 2006 Decreasing Russia (Murman coast) <500 1998 Unknown Norway (East Finnmark) 207 2003-2005 Decreasing Norway (West Finnmark to 62°N) 5485 2003-2005 Decreasing Norway south of 62°N 685 2003-2006 -40% Norwegian Skagerrak 291 2005-2009 +20% Swedish Skagerrak 2689 2005-2009 +40% Kattegat 6182 2005-2009 +15 % Baltic (Kalmarsund) 592 2005-2009 + 30% Southern Baltic 527 2005-2009 + 20% Limfjord 879 2005-2009 - 4% Wadden Sea Denmark 3063 2005-2009 +10% Wadden Sea Germany 11680 2005-2009 +10% Wadden Sea Netherlands 6339 2005-2009 +10% Faroes 0 UK Shetland 3021 2001-2006 -40% UK Orkney 4256 2001-2006 -45% UK Scotland east 1819 1997-2006 -26% UK England east 3617 2001-2006 -34% France 239 2005-2006 Slight increase Extinct Source: Diverse 13 Policy Department B: Structural and Cohesion Policies Table 2: Abundance of grey seals in the North-East Atlantic. *Numbers of pups x 4.5 LOCATION COUNT YEAR CHANGE OVER PAST 5 YEARS Iceland 4950 1997-2007 -30% Russia (Murman coast) 2427* 1991-1992 Unknown Norway (East Finnmark) 670* 2001-2006 +30% Norway (West Finnmark-62°N) 5000* 2001-2006 Unknown Norway (South of -62°N) 158 2001-2006 Stable Skagerrak 5 2006-2009 Stable Kattegat 21 2006-2009 Stable Baltic 22050 2006-2009 Stable Wadden Sea 2194 2006-2009 +100% France 90 2005 Stable Faroes <500 2005 Decreasing UK Shetland 3047* 2006 Stable UK Orkney 86994* 2002-2006 +1.5% UK North Sea colonies 5322* 2002-2006 +20% TOTAL 133428 Source: Author; ICES (2004); Anon. (2008) 1.1.2. Potential or likely impacts on fish stocks in oceanic ecosystems Impacts of seals on fish stocks can be significant in ecosystems where seals are highly abundant. It is estimated that the 2.06 million harp seals in the Barents Sea consume 3.5-5 million tonnes of krill and fish (Lindstrøm et al., 2006). The composition of the diet varies among years and is linked to large scale ecosystem dynamics. The most important fish prey species are polar cod, cod and capelin (Nilssen et al., 2000), and seal predation can under some modelled scenarios have effects on prey species (Bogstad et al., 1997). However, the model was more sensitive to changes in food preferences of cod than changes in diet or abundances of marine mammals (Bogstad et al., 1997). The Norwegian coast was invaded by large numbers of harp seals in 1987 (crash in capelin stocks) and dietary analyses showed a dominance of cod, capelin, saithe and herring (Ugland et al., 1993). It was estimated that 110 million individuals of cod and saithe of year classes 1985 and 1986 were consumed by harp seals. These year classes were later found to be severely depleted (Ugland et al., 1993). Consequently, very abundant stocks of seals (millions) may have measurable impacts on fish stocks they prey upon also in oceanic ecosystems. 14 Seals and fish stocks in the North-East Atlantic 1.2. Impacts on environments fish stocks in coastal and estuarine Both grey and harbour seals are confined to coastal areas during reproduction and moult. They also show explicit site fidelity to specific haul-out sites, from where they make foraging trips. Whereas harbour seals seldom travel more than 100 km (Figure 2), grey seals may travel more than 500km (McConnell et al., 1999). However, both species also forage in the vicinity of their haul-out sites, and high local densities of seals can in some cases lead to competition with specific fisheries, although a general impact on coastal stocks have not been demonstrated. Some investigations have shown that foraging areas of harbour seals and grey seals often overlap with areas used by coastal fisheries (e.g. Bjørge et al., 2002). Seal predation on fish species, such as cod, also targeted by the fisheries are assumed to reduce catches (Bjørge et al., 2002), which may be true, but there is no information available on extent to which seals reduce local fish stocks. Figure 2: Harbour seals tagged with satellite transmitters in the Danish Wadden Sea can forage over extensive areas, but also in the vicinity of their haul-out sites Source: http://www.hornsrev.dk/ Investigations in the Limfjord (Denmark) and the Southern Baltic showed that seals mainly targeted non-commercial fish species apart from Atlantic herring which was the most important species. The competition with the fisheries was regarded minor or insignificant (Andersen et al., 2007). The impact of seal predation on local salmon or trout stocks in river mouths varies with the size of local seal stocks, fish abundance, and fishing mortality caused by the fishery (Carter et al., 2001). Although seal predation on salmonids in many Scottish estuarine environments is ten-fold less than that caused by the fishery (Carter et al., 2001), it was shown in one case that removal of some seals increased the catches by 30% (Butler et al., 2006). Tornijoki river in the Northernmost part of the Baltic is one of the most important spawning rivers for salmon in the Baltic and it is indicated that seal predation in the river mouth could reduce numbers of salmons entering into the river by 20% (Juonela et al., 2006). 15 Policy Department B: Structural and Cohesion Policies 16 Seals and fish stocks in the North-East Atlantic 2. IMPACTS ON CATCHES AND FISHING GEAR KEY FINDINGS Fisheries using active gear in offshore areas, contributing to about 90% of landings in the North-East Atlantic, have minor or insignificant impacts from seals on gear and catches. Some fisheries using active gear close to the coast experience losses to seals that can exceed 10% of catches. Artisanal fisheries based on angling and encircling gillnets generally show low impacts of seals. Set gillnets and drift nets are very vulnerable to seals. Catch losses can exceed 50% in gillnets set for cod, herring and white fish in the Baltic Sea, whereas lower loss rates are reported in other parts of the North-East Atlantic. Gillnets are difficult to protect against seals since acoustic deterrents, which may have effects initially, eventually become ineffective and might even attract seals. Bagnets, fish traps and fykenets are vulnerable to seals, and in the Baltic where these types of static gear are commonly used, seal-fisheries interactions are severe and losses exceed 6 million € only in the Swedish fishery. Modifications of fish traps have successfully reduced damages to catch and gear. Shooting of seals has not significantly reduced damages to catches or gear in the Baltic. The impact of seals on catches and fishing gear is highly variable and is affected by a number of factors, of which type of used gear and geographical location of fishing operations in relation to densities of seals are the most important parameters. Here the structure of the fishery is a critical factor since the offshore fishery using active gear is affected to a minor or insignificant extent by seals, whereas fisheries based on specific types of passive gear in coastal areas are influenced by seal predation and damage to fishing gear to a much greater extent. Many types of static gear such as bag nets and fish traps or fyke nets (eel) used in regions such as the Baltic Sea and the Limfjord (Denmark), are not commonly used in other parts of the North-East Atlantic. These types of gear are less suitable for fishing in tidal areas with strong currents and large fluctuations in water levels. The offshore fisheries using active gear such as pelagic or bottom trawls dominate the fisheries in the North-East Atlantic and take about 90% of the total catches. However, catches in the coastal fisheries are to a greater extent focussed on providing fish for human consumption, which is why the economic value of these catches are greater than the 10% of the total landings. This can be illustrated by the situation in the Swedish fisheries, where coastal or Baltic fisheries using passive gear contribute by 15% to the total economic value of the fisheries (Figure 3). Much of this fishery is severely affected by seals. 17 Policy Department B: Structural and Cohesion Policies Figure 3: Fisheries using passive gear operating vessels < 12m contribute by 13%, and larger vessels by 2% to the economic value of the Swedish fisheries. Relative economic value of different Swedish fisheries Passive gear<12m Passive gear>12m Nephrops trawl Shrimp trawl Other bottom trawls Pelagic trawls < 40 m Pelagic trawls > 40 m Source: Swedish Board of Fisheries (2009) 2.1. Impacts in oceanic ecosystems Most reports on interactions between seals and fisheries operating offshore mention that seals sometimes get caught in pelagic trawls or bottom trawls, which appears to be the main negative effect for the offshore fisheries (Morizura et al., 1999). Information on impacts of seals on catches and gear is very scarce and appears to be minor or insignificant. 2.2. Impacts in coastal and estuarine environments Many different fishing methods have been developed in coastal regions of the North-East Atlantic of which a majority use some type of static gear. However, in some regions Nephrops and shrimp trawls are towed close to the shore, and some of these fisheries report interactions with seals that damage by-catches of cod and hake although gear damage was minor (Moore, 2003). 2.2.1. Angling Angling is basically not used by professional fishermen, but is important for the recreational fishery. Anglers occasionally report interactions with seals, but their main complain is that seals and anglers compete for the same resource, especially for salmon, trout and some white fish. 2.2.2. Encircling gill nets Encircling gillnets have been used for thousands of years and much of the fishery in the North-East Atlantic, e.g. during the herring periods was based on this method. It was the 18 Seals and fish stocks in the North-East Atlantic most common fishing method in the North-East Atlantic until the Middle Ages, but was still extensively practised in Scandinavia until the 18th century (Figure 4). Diminishing fish stocks made this method unprofitable and the fishing effort was gradually allocated further offshore. However, encircling gill nets are still common in artisanal fisheries worldwide, and is practised in river mouths in Scotland to catch salmon. This type of fishery seldom report impacts by seals on gear or catches. Figure 4: Encircling gillnets have been used as a main fishing method for thousands of years Source: Laksefiskaren (Salmon fisherman) painted by Elif Peterssen (1889) 2.2.3. Set gillnets Small scale fisheries using gillnets are generally not very common in the North-East Atlantic, whereas fisheries along the Scandinavian coasts and the Baltic to a great extent use gillnets to target specific species of fish such as cod, herring and white fish (Fjälling, 2006). This fishery reports substantial damage to gear and catches and losses to seals may exceed 50% of the catches under some circumstances. A dedicated study on a cod gillnet fishery in the Baltic showed that such losses could vary from 67% of the landed catches in the gill net fishery in 2005 to 19% in 2006 (Königson et al., 2009). A similar situation is seen in the gillnet fisheries focussing on Baltic herring, experiencing substantial losses to grey seals, and where damages to nets are very common (Figure. 5). 2.2.4. Bag nets and fish traps Also bag nets, fish traps and fykenets are less commonly used in tidal areas, which is why problems with seals in this type of fishery are not significant in e.g. the Wadden Sea and the incidents are very limited compared with the Skagerrak, Kattegat and the Baltic where such gear are commonly used. There have been increasing interactions between grey seals and the coastal trapnet fisheries for salmon and white fish in the Northern part of the Baltic (the Bothnian Bay), where catch losses have ranged between 3% and 29% (Juonela et al., 2006), whereas other studies found that losses could be as high as 61% (Fjälling, 2005). 19 Policy Department B: Structural and Cohesion Policies Figure 5: A grey seal raiding a herring gillnet in the Baltic Source: Fjälling (2005) 2.3. 2.3.1. Mitigation measures Protective hunting Slightly more than 800 grey seals and 50 harbour seals were shot in the Baltic, the Skagerrak, the Kattegat in 2009 (Helcom website). Effects of this protective hunting have not been evaluated recently, but earlier investigations indicate that this type of hunting has limited or no effects on damages caused by seals on catches and gear (Sand and Westerberg, 1997). 2.3.2. Modification of fishing gear Simple modifications of salmon traps have proved to efficiently reduce losses to seals and reduced gear damages considerably. A wire grid in the funnel of the trap in combination with stronger net in the bag reduced losses by 70% as compared with traditional traps (Lehtonen and Suuronen, 2004). Other modifications such as increasing the mesh size of side panels of salmon traps substantially reduced damages to catch and gear (Lunneryd et al., 2003). Using stronger nets in fyke nets set for eel and preventing seals from entering into traps have considerably reduced interactions with seals (Fjälling, 2006). Modification of fishing gear has thus proved to be the most efficient way to reduce damages caused by seals. 20 Seals and fish stocks in the North-East Atlantic 2.3.3. Acoustic deterrants Acoustic harassment devices are extensively used in Scottish fish farms, but proper evaluations on their effectiveness are not available (Quick et al., 2004). Such evaluations have been done in the Baltic, where it was found that acoustic harassment devices reduced interactions with seals initially, but that positive effects diminished with time (Fjälling et al., 2006). Other studies even suggest that acoustic deterrents may attract grey seals to gillnets (Stridh, 2008), which is why such devices are unlikely to substantially contribute to mitigations between seals and fisheries in the future. 21 Policy Department B: Structural and Cohesion Policies 22 Seals and fish stocks in the North-East Atlantic 3. SPREAD OF PARASITES WHERE SEALS ACT AS FINAL HOSTS KEY FINDINGS Whale worms (Anisakis simplex) and seal worms (Pseudoterranova decipiens) are commonly confused in the general understanding of the impact of seals on the prevalence of parasites in commercially important fish species. Whale worms are predominantly spread by harbour porpoises, dolphins and minke whales, whereas seal worms are spread by grey seals, bearded seals, harp seals and harbour seals. Larval stages of both whale worms and seal worms occur in the fillets of commercially important fish species, and removal of the parasites cause considerable costs to the fish processing industry. Since reports from the fisheries do not distinguish between whale worms and seal worms, it is not possible to evaluate the contribution of seal worms in this context. The frequency of whale worms exceeds 90% in cod from Iceland, Barents Sea and the Celtic sea. The contribution of seals to this situation is minor or insignificant. Burdens of seal worms are very low in fish caught offshore, whereas fish caught inshore close to seal colonies can be heavily infected. The occurrence of seal worms in coastal areas is limited by the availability of intermediate invertebrate hosts, fish species such as sea scorpion accumulating seal worm larvae, and sometimes, but not always the size of the seal population. Both grey seals and harbour seals are final hosts for a number of parasites such as tape worms (Cestoda), hook worms (Acanthocephala) and Anisakid nematodes. Tape worms and hook worms infest the seals, but seldom cause any problems for the marine fisheries, which is why this review will focus on Anisakid nematodes. The most common nematodes found in seals are Pseudoterranova decipiens (seal worm, cod worm), Contracaecum osculatum, Phocascaris cystophorae and Anisakis simplex (whale worm, Figure 6). Larval stages of C. osculatum and Ph. cystophorae appear in the gut or abdominal cavities of many fish species, and can in some cases penetrate the skin in deteriorating fish. However, those parasites are normally removed when the fish is rinsed, and losses for the fishery caused by these two species are minor or insignificant. Inactive larval stages of whale worm are often found as incapsulated spirals on the liver or intestines of mackerel, herring and other species of fish (Figure 6). Larvae can also be abundant in the muscle of cod where prevalence of 96% has been reported from the Barents Sea (Aspholm, 1995). Removal of whale worms from fillets constitutes significant costs for the fish processing industry. However, toothed whales are the main final hosts of the whale worm, which appears in most oceans, and densities of this parasite seem to be predominantly affected by the occurrence of harbour porpoises and dolphins. Although whale worms develop in seals to the adult stage, seals are indicated to be suboptimal final hosts since the size of the adult stage of A. simplex is considerably smaller in seals as compared with toothed whales. Whale worms are often confused with seal worms and the confusion is accentuated by the Norwegian word “kveis” being used both for whale worm and seal worm. 23 Policy Department B: Structural and Cohesion Policies Figure 6: Whale worm (Anisakis simplex) in the abdominal cavity of a mackerel, but it is also common in herring and cod. Although seals act as final hosts for whale worm, toothed whales such as harbour porpoises and dolphins are indicated to be more important for the occurrence of whale worm in fish. Source: Author The seal worm is by far the most important parasite spread by seals and causes considerable economical costs for some fisheries, although there are substantial differences among regions as well as among fish species. Grey seals, harbour seals, bearded seals and harp seals are final hosts for the seal worm in the Barents Sea and the North-East Atlantic. The seal worm represents a species complex and genetic analyses have identified three sibling species: Pseudoterranova decipiens A infecting grey seals, P. decipiens B infecting harbour seals, and P. decipiens C infecting bearded seals (Paggi et al., 1991). In all sibling species the adult worm shed eggs in the intestine of their host, and the eggs are shed to the sea with the faeces. When the eggs are ingested by invertebrate intermediate hosts such as benthic small crustaceans and polychaetes, the egg starts developing and passes a number of larval stages. If the intermediate host is ingested by a fish, the larvae transform to the third stage and remain so even if the fish is ingested by a predatory fish. The larvae are mostly found in the muscle and in greatest abundances in sea scorpion, bullroute, and bullheads, which act as important reservoirs for seal worm larvae. Commercially important fish species feeding on these benthic species can therefore be heavily infected, whereas others such as mackerel or salmon very rarely get infected. When infected fish is consumed by a seal, larvae transform to the adult stage. It is the third stage larvae that cause problems to the fishery, since they are found in the muscle and must be removed manually. Consequently, the prevalence or abundance of seal worms in commercially important fish species is affected partly by seal density and abundance, but also by the presence/absence of intermediate invertebrate hosts, and by species such as sea 24 Seals and fish stocks in the North-East Atlantic scorpion, which accumulate the larvae. A general pattern is that the occurrence of seal worms in fish is greatest in fish caught close to seal colonies, whereas fish caught further away often are uninfected (Jensen and Idaas, 1992). 3.1. Seal worm in fish in oceanic ecosystems The frequency of seal worm in commercially important species caught in offshore fisheries in the North-East Atlantic is generally low (Hemmingsen and MacKenzie, 2001) and constitutes a minor problem to the fisheries. The situation is somewhat different in the Barents Sea and adjacent areas where harp seals are very abundant. However, the main problems with seal worm are found in the coastal fisheries. Figure 7: Location of cod samples taken for analyses of whale worm and seal worm Source: Alonso (2008) 25 Policy Department B: Structural and Cohesion Policies Table 3: Frequency (%) and mean numbers (brackets) of whale worm (Anisakis simplex) and seal worm (Pseudoterranova decipiens) in east Atlantic cod LOCATION A. simplex P. decipiens Sample size Baltic 15 (2.3) 3.9 (0.07) 180 North Sea and Skagerrak 50.3 (34.3) 12.9 (1.4) 147 Celtic Sea 92 (74.9) 0.8 (2.2) 138 Irish Sea 36 (4.6) 22.1 (0.9) 136 Trondheimsfjord 5 (0.05) 1.7 (0.02) 60 Iceland 99.4 (327) 0.7 (3.1) 165 Barents Sea 96 0 Not given Data source: Alonso (2008) and Aspholm (1995). 3.2. Seal worm in coastal ecosystems The occurrence of seal worms shows very large variations along the coasts of Iceland and Norway (e.g. Andersen et al., 1995; Hemmingsen and MacKenzie, 2001; Figure 7, Table 3). In some areas with large colonies of seals the frequency of infestation is high especially in cod. In those regions processing plants scan each filet for seal worm, which increases the processing cost, whereas in other Icelandic and Norwegian regions the problems with seal worm are insignificant or minor. Although more seal worms in fish occur close to haul-out site of seals, the problems for the coastal fisheries vary substantially depending on which type of gear is used and migration patterns of targeted fish species (Andersen et al., 1995; Alonso, 2008, Table 3). However, decreasing numbers of seals in some areas have resulted in lower infestation rates (des Clers and Andersen, 1995; Hauksson, 2002), suggesting that local high densities of seals is linked to infestation rates in demersal relatively stationary fish species. The frequency of seal worm in cod from the Skagerrak and the Kattegat is generally low (Andersen et al., 1995, des Clers and Andersen, 1995) Consequently, seal worm is a minor problem for fisheries using active gear, but the parasite can be locally abundant especially in cod caught in passive gear in areas with high densities of seals. 3.3. Seal worm in estuarine and brackish water ecosystems Larval stages of the seal worm develop also in sub zero temperatures and are present in the Arctic as well as in the Antarctic (Palm, 1999). However, its distribution seems to be severely restricted in brackish water systems as the Baltic Sea. It has been found in cod caught in the southern part of the Baltic (Perdiguero-Alonso et al., 2008), but only in small numbers. A possible reason for its low occurrence in brackish water systems may be lack of suitable intermediate hosts. Another reason could be that species accumulating larvae, such as sea scorpion, are not present in these ecosystems. Consequently, seal worm may occur in brackish water systems, but its distribution and prevalence is predicted to be low in such environments. 26 Seals and fish stocks in the North-East Atlantic 4. AQUACULTURE KEY FINDINGS The first-hand value of fish farmed in the North East Atlantic exceeds 3 Billion €, and aquaculture is a rapidly increasing industry. Losses to seals in fish farms in Norway, Iceland and the Faroes are less than 1%, whereas losses in Scotland are estimated at 1-5%. Shooting and predator nets are the most common mitigation methods, but acoustic deterrents are also used in Scotland. Shooting of seals is an effective mitigation method if the hunt is intense enough to deplete local seal populations. Scottish, Icelandic, and Norwegian populations of harbour seals are decreasing as a consequence of excessive hunting. The Faroese harbour seal population is extirpated. Finfish farming is a rapidly growing (10-15% per year) industry and the current firsthand value of produced fish, predominantly salmon and trout, exceeds 3 billion € in the North-East Atlantic (Table 4). Most fish farms are found in Norway and Scotland, where they are situated in fiords which give them protection against high waves and strong currents. Most fish farms are visited by seals, but the loss and damage caused by seals vary greatly among farms (Quick et al. 2004). Table 4: Production of farmed salmon and trout in the North-East Atlantic. Losses to seals and mitigation method *Inferred from 8.5 million smolts delivered to fish farms. Shooting is the most common mitigation method in all countries, whereas Acoustic Harassment Devices (AHD) or Acoustic Deterrent Devices (ADD) are predominantly used in Scotland. PRODUCTION (tonnes) FIRST HAND VALUE YEAR LOSS TO SEALS MITIGATION METHOD Norway 980,000 2,400 million € 2009 <1% Shooting Predator net Iceland No info No info - <1% Shooting Predator net Denmark 40,415 92 million € 2008 <1% Shooting Predator net Faroes* 25,000 68 million € 2009 < 1% Shooting Scotland 135,000 500 million € 2009 1-5% Shooting Predator net AHD, ADD COUNTRY Source: Author; Fiskeridirektoratet (2010); Quick et al. (2004) 27 Policy Department B: Structural and Cohesion Policies 4.1. Interactions with seals and mitigation measures The impact of seals on fish farms is comparatively low in Norway, Iceland and the Faroes, where a combination of shooting of seals and predator nets are practised. However, to be effective, lethal removal of seals must be large enough to reduce seal populations in the vicinity of the farms. There are no colonies of seals in fiords used for fish farms in Norway and the Faroes and occasional visiting seals are shot. As a consequence of this type of antipredator strategy, in the Faroes the harbour seals have been extirpated and the total population of grey seals is below 500 animals. About 200-250 grey seals, of which a majority is believed to come from Scottish seal colonies, are shot annually as a part of a protection programme for the aquaculture (ICES, 2004). Also the Icelandic seal hunt has resulted in decreasing seal populations, whereas the hunting in Norway balances the recruitment in both harbour seals and grey seals in some areas, but decreasing numbers are seen in others (Table 2). Shooting of seals is also practised in Scotland and the annual 2-5% reduction in harbour seal numbers in The Moray Firth over the last decade would be explained by the annual removal of 66–327 harbour seals at salmon fisheries and fish farm sites (Thompson et al., 2007). A Scottish study (Quick et al., 2004) investigated how fish farmers experienced different types of protective measures against seal predation and 190 out of 195 used some kind of anti predator controls (Table 5). Seals were reported to have visited 81% of the farms, but losses caused by seals have been constant over the period 1987-2001. Shooting was practised at 73 sites and was considered to be effective by a majority, whereas acoustic seal scarers were considered as less effective. Predator nets were experienced as effective at some farms but not at others. Table 5: Effectiveness of anti-predator controls in Scottish fish farms No OF SITE MANAGERS CONSIDERED EFFECTIVE Shooting 73 62% Seal scarers 92 23% 180 varying METHOD Predator nets Source: Quick et al. (2004). 4.2. Considerations The most effective mitigating measure is to place fish farms far away from larger colonies of seals, since there is a strong correlation between distance to seal haul-out sites and intensity of damage caused by seals (Kashner et al., 2006). This feature should be considered in detail before establishing fish farms in the future. Another effective way to protect fish farms is to shoot seals, but hunting has to be carried out to an extent where seal populations get depleted. This is not always a desirable option especially since the EU-habitats Directive states that the long-term 28 Seals and fish stocks in the North-East Atlantic objectives for the management of marine mammals are “Natural abundance, natural distribution, and a health status that ensures their future persistence”. It is also stated that these long-term objectives should not be affected by socioeconomic considerations, although such considerations could be taken in the implementation of management plans. These basic components are also the basis for the 2006 HELCOM recommendation, which has been ratified by all Baltic countries. 29 Policy Department B: Structural and Cohesion Policies 30 Seals and fish stocks in the North-East Atlantic REFERENCES Alonso, D.P. (2008), Parasite communities of the European Thesis.Universitat de Valencia, Department de Zoologia, 160 pp Andersen K., des Clers S., Jensen T. (1995), Aspects of the sealworm Pseudoterranova decipiens life-cycle and seal-fisheries interactions along the Norwegian coast. Developments in Marine Biology 4: 557-564. Whales, seals, fish and man, Proceedings of the International Symposium on the Biology of Marine Mammals in the North East Atlantic , 29 November-1 December 1994. Andersen S.M., Teilmann J., Harders P.B., Hansen E.H., Hjøllund D. (2007), Diet of harbour seals and great cormorants in Limfjord, Denmark: interspecific competition and interaction with fishery. ICES Journal of Marine Science 64, 1235–1245. 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(2006), Interactions between grey seal (Halichoerus grypus), Atlantic salmon (Salmo salar), and harvest controls on the salmon fishery in the Gulf of Bothnia. ICES Journal of Marine Science 60: 1194-1199. Kaschner K., Karpouzi V., Watson R., Pauly D. (2006), Forage fish consumption by marine mammals and seabirds, p. 33-46. In: Alder, J., Pauly, D., (eds). On the multiple uses of forage fish: from ecosystems to markets. Fisheries Centre Research Reports 14(3). Fisheries Centre, University of British Columbia [ISSN 1198-6727]. 32 Seals and fish stocks in the North-East Atlantic Königson S., Fjälling A., Lunneryd S.G. (2005), Impact of grey seals in the herring gillnet fishery along the Swedish Baltic coast. Institute of Coastal Research, Swedish Board of Fisheries. 7p. Königson S., Fjälling A., Lunneryd S.G. (2007), Grey seal induced catch losses in the herring gillnet fisheries in the northern Baltic. NAMMCO Sci. Publ., 6: 203–213. Königson S., Lunneryd S.G., Stridh H., Sundqvist F. (2009), Grey seal predation in cod gillnet fisheries in the central Baltic Sea. J. Northw. Atl. Fish. Sci. 42: 41–47. Lehtonen E., Suuronen P. (2004), Mitigation of seal-induced damage in salmon and whitefish trapnet fisheries by modification of the fish bag. ICES Journal of Marine Science. 61, 1195-1200. Lindstrøm U., Nilssen K.T., Haug T. (2006), Prey consumption by Barents Sea harp seals in the period 1990-2005. ICES CM 2006 / L:08 Lundström K., Hjerne O., Lunneryd S.G., Karlsson O. (2010). Understanding the diet composition of marine mammals: grey seals (Halichoerus grypus) in the Baltic Sea. ICES Journal of Marine Science 67/6, 1230-1239. Lunneryd S.G., Fjälling A., Westerberg H. (2003), A large-mesh salmon trap: a way of mitigating seal impact on a coastal fishery. ICES J. Mar. Sci. 60, 1194-1199. McConnell B., Fedak M.A., Lovell P., Hammond P.S. (1999), Movements and foraging areas of grey seals in the North Sea. Journal of Applied Ecology 46, 573-590. Mikkelsen B., Haug H., Nilssen K.T. (2002), Summer Diet of Grey Seals (Halichoerus grypus) in Faroese Waters. Sarsia 87, 462 – 471. Moore P.G. (2003), Seals and fisheries in the Clyde Sea area (Scotland): traditional knowledge informs science. Fisheries Research 63, 51-61. Morizura Y., Berrow S.D., Tregenzac N.J.C., Couperusd A.S., Pouvreaua S. (1999), Incidental catches of marine-mammals in pelagic trawl fisheries of the northeast Atlantic. Fisheries Research 41, 297-307. Nilssen K.T., Pedersen O.P., Folkow L.P., Haug T. (2000), Food consumption estimates of Barents Sea harp seals. NAMMCO Scientific Publications 2, 9-27. Olafsdottir D., Hauksson E. (1997), Anisakid (Nematoda) Infestations in Icelandic GreySeals (Halichoerus grypus Fabr.) J. Northw. Atl. Fish. Sci. 22, 259–269. Paggi L., Nascetti G., Cianchi R., Orecchia P., Mattiucci S., D'Amelio S., Berland B., Brattey J., Smith J.W., Bullini L. (1991), Genetic evidence for three species within Pseudoterranova decipiens (Nematoda: Ascaridida, Ascaridoidea) in the North Atlantic and Norwegian and Barents Seas. International Journal for Parasitology 21,195-212. Palm H.W. (1999), Ecology of Pseudoterranova decipiens (Krabbe, 1878) (Nematoda: Anisakidae) from Antarctic waters. Parasitology Research 85, 638-646. Perdiguero-Alonso D., Montero F.E., Juan Antonio Raga J.A. (2008), Composition and structure of the parasite faunas of cod, Gadus morhua L. (Teleostei: Gadidae), in the North East Atlantic. Parasites & Vectors 2008 1,23. Prime J.H., Hammond P.S. (1990), The diet of grey seals from the south-western North Sea assessed from analyses of hard parts found in faeces. Journal of Applied Ecology 27, 435-447. Quick NJ, Middlemas SJ, and John D. Armstrong JD. (2004), A survey of antipredator controls at marine salmon farms in Scotland. Aquaculture 230, 169-180. 33 Policy Department B: Structural and Cohesion Policies Stridh H. (2008), Can grey seal (Halichoerus grypus) learn to use acoustic deterrants to locate fishing gear? Master Degree project. Department of System ecology, Stockholm University & Swedish Board of Fisheries. Thompson P.M., Mackey B., Barton T.R., Duck C., Butler J.R.A. (2007), Assessing the potential impact of salmon fisheries management on the conservation status of harbour seals (Phoca vitulina) in north-east Scotland. Animal Conservation 10, 48–56. Ugland K.I., Jødestøl A., Aspholm P.E., Krøyer A.B., Jakobsen T. (1993), Fish consumption by invading harp seals off the Norwegian coast in 1987 and 1988. ICES J. Mar. Sci. 50, 27-38. 34 Seals and fish stocks in the North-East Atlantic NOTES 35