0-group Fish Research Articles

The Dynamics of 0-Group Herring Clupea harengus and Sprat Sprattus sprattus Populations Along the Norwegian Skagerrak Coast

Coastal areas are important habitats for early life stages of many fish species. These habitats are used as nursery grounds and can provide a significant contribution to the recruitment of a fish population. In 1919, standardized sampling with a beach seine along the Norwegian Skagerrak coastline was established mainly to target 0-group fish. Here, we focus on Atlantic herring and European sprat to explore whether inter-annual variability in the abundance of these species is indicative of variability in recruitment. We investigated if the abundance of 0-group herring and sprat are affected by environmental factors. Further, the beach seine abundance indices were compared with recruitment estimates of neighboring stocks. There was a clear correlation between herring and sprat abundance in the beach seine samples. While sprat abundance was mainly affected by environmental factors such as temperature and current drift, herring abundance was positively affected by the recruitment of the neighboring stock of western Baltic spring spawners. One plausible explanation could be that sprat recruit to a more local component, while herring of the neighboring stock utilize the Skagerrak coastline as nursery grounds. This study demonstrates the importance of long time series and can provide new insight into the dynamics and structure of multiple fish species.

Recruitment variability of fish stocks in the Barents Sea: Spatial and temporal variation in 0-group fish length of six commercial species during recent decades of warming (1980–2017)

Young-of-the-year (0-group) fish in the Barents Sea have been investigated in an annual joint Norwegian-Russian pelagic trawl survey in autumn, using a standardized procedure since 1980. We use a conceptual framework of ‘upstream’ spawning areas and ‘downstream’ nursery areas, recorded as 0-group distribution in the Barents Sea, to address spatial (geographical) and temporal (1980–2017) variation in 0-group length. Four boreal species (cod Gadus morhua, haddock Melanogrammus aeglefinus, herring Clupea harengus, and deepwater redfish Sebastes mentella) tended to have smaller 0-group individuals in the northern and eastern parts of the Barents Sea, with the largest individuals found in the central part where they were also most abundant. We interpret this to reflect slower growth as the ‘fore-runners’ of the seasonal cohort of juveniles are transported into colder waters (through lateral mixing). The Arctic species (capelin Mallotus villosus and polar cod Boreogadus saida) showed a different pattern with increasing 0-group length with increasing distance away from the spawning areas, seen most clearly for capelin. The longer juveniles in northern areas are probably older and stemming from early spawning.There was temporal covariation in 0-group length between the six species over the 38-year time series, with highest correlation between cod and haddock. The covariation reflected similar fluctuations in four decadal ‘waves’, with maxima in 0-group length in the early/mid 1980s, 1990s, 2000s, and 2010s. There was a high degree of spatial consistency in the temporal patterns of variation in 0-group length, with synchronous variations in different geographical areas. There were also increasing linear trends over the time series for cod, haddock, and polar cod, which represented increase of about 20%, 40%, and 15% of the initial length for the three species, respectively. The fluctuations and trends in 0-group length were positively correlated with seawater temperature, which suggests a strong effect of climate variability and warming (by 1.5–2.0 °C since 1980) on 0-group length. The clear differences among the species, and the limited fraction of variance explained by temperature, suggest that other factors such as food play additional roles. Zooplankton biomass integrated over the water column had low explanatory power, but this may reflect intrinsic limitations in the data (e.g., depth-integrated, end of season) in providing an adequate representation of feeding conditions, rather than suggesting that food was not important.

Distribution of rorquals and Atlantic cod in relation to their prey in the Norwegian high Arctic

Recent warming in the Barents Sea has led to changes in the spatial distribution of both zooplankton and fish, with boreal communities expanding northwards. A similar northward expansion has been observed in several rorqual species that migrate into northern waters to take advantage of high summer productivity, hence feeding opportunities. Based on ecosystem surveys conducted during August–September in 2014–2017, we investigated the spatial associations among the three rorqual species of blue, fin, and common minke whales, the predatory fish Atlantic cod, and their main prey groups (zooplankton, 0-group fish, Atlantic cod, and capelin) in Arctic Ocean waters to the west and north of Svalbard. During the surveys, whale sightings were recorded by dedicated whale observers on the bridge of the vessel, whereas the distribution and abundance of cod and prey species were assessed using trawling and acoustic methods. Based on existing knowledge on the dive habits of these rorquals, we divided our analyses into two depth regions: the upper 200 m of the water column and waters below 200 m. Since humpback whales were absent in the area in 2016 and 2017, they were not included in the subsequent analyses of spatial association. No association or spatial overlap between fin and blue whales and any of the prey species investigated was found, while associations and overlaps were found between minke whales and zooplankton/0-group fish in the upper 200 m and between minke whales and Atlantic cod at depths below 200 m. A prey detection range of more than 10 km was suggested for minke whales in the upper water layers.

The Record-Warm Barents Sea and 0-Group Fish Response to Abnormal Conditions

The Barents Sea is a nursery area for many fish stocks, and this whole region is presently subject to rapid climatic change from a cold period in the 1980s to a record warm period in the latest decade, with a peak in 2016. The present study focuses exclusively on year 2016, which was characterized by record warm air and seawater and an exceptionally large horizontal coverage of Atlantic waters. Earlier studies have suggested that environmental conditions during the first year of life are the most critical for year class strength and development of fish stocks. We focus on 8 fish species (age 0) and document spatial distributions of their abundances and lengths as well as ambient environmental conditions. Data for most of the Barents Sea obtained from the ecosystem survey were used to explore if the record-warm conditions in 2016 limited 0-group fish distributions, abundances and size. Abundances and lengths for the 8 species were related to physical conditions (seawater temperature and salinity) and biological features (mesozooplankton biomass and jellyfish biomass). In 2016, 0-group capelin, haddock, herring and long rough dab were more abundant and all species except long rough dab were larger than the long term mean (1980-2015). Larger individuals and higher abundances were observed mainly in the areas covered by relatively warm water masses apparently holding a sufficient amount of plankton. Most of the 0-group fishes were distributed within their thermal habitats, but with some geographical shift most likely reflecting a shift in the distribution of water masses. A significantly lower abundance of polar cod was observed in 2016, with very few individuals registered within the traditional core area in the south eastern Barents Sea. The increased temperature and low plankton biomass may have limited polar cod distribution and abundance there. A spatial analysis showed that biomass of C. capillata was positively related to abundances of 0-group herring, capelin and cod, indicating that they were inhabiting similar water masses. The high abundances of capelin, haddock, herring and long rough dab, and generally large individuals of most species, may suggest suitable living and feeding conditions in 2016

Environmentally Driven Ecological Fluctuations on the Faroe Shelf Revealed by Fish Juvenile Surveys

Comprehensive late June surveys have for decades been carried out on the Faroe shelf in order to estimate the abundance of juvenile fish – the 0-group. The abundance of cod juveniles has previously been used in recruitment studies, while the ecological implication of the 0-groups has hitherto received less attention. Here we examined the pelagic 0-group stage in four of the main fish species on the Faroe shelf: cod, haddock, Norway pout and sandeel, representing more than 90% of all juvenile fish on the shelf. A positive relationship between length and abundance at the 0-group stage is observed for all juveniles, and the inter-annual variability was highly similar among the four fish species. Based on this knowledge, we produced a new ecological indicator for the central Faroe shelf ecosystem - the 0-group length index. The 0-group length index is characterized by marked peaks in 1984, 1987, 1994, 2000, 2009 and 2017, which appear to be related to the shelf primary production from spring to mid-summer, and possibly to the marine climate surrounding the Faroe shelf. There is a better temporal overlap between the fish larvae and their prey (i.e. small- to medium sized zooplankton) in years with an early and intensive bloom, while late and/or weak blooms lead to unfavorable feeding conditions. We furthermore show that a large abundance of 0-group fish has the potential to graze down and thus regulate the biomass of large-sized zooplankton during late June. In addition to this top-down influence the 0-group fish clearly impact commercial fish stocks and seabird colonies, and our 0-group length index is therefore a key ecological indicator for the state of the entire central Faroe shelf ecosystem.

Feeding Ecology of Zero Group Fish Community from Shatt Al-Arab River in Basrah, Iraq

The food and feeding adaptations of 0-group fishes in the water of Shatt Al-Arab River were studied during the period between March 2011 to December 2012. A total of 1851 fish samples of were collected. The stomach fullness and contents were observed and analyzed using frequency of occurrence, numerical and point methods. The non-empty stomach recorded during the study could be attributed to food abundance and good feeding habits. Four major food groups Bacillariophyta, Chlorophyta, Cyanophyte, Copepods, Amphipods and Shrimp) were recorded. The result showed that Liza subviridis is herbivores and the remaining of the fish are omnivores feeders. The degree dietary overlap among the species investigated was in the region of 51.1% . Diet Similarity Index between each pair species was also calculated .The results indicate that these fish might be in direct competition for food.

Biomass of Scyphozoan Jellyfish, and Its Spatial Association with 0-Group Fish in the Barents Sea

An 0-group fish survey is conducted annually in the Barents Sea in order to estimate fish population abundance. Data on jellyfish by-catch have been recorded since 1980, although this dataset has never been analysed. In recent years, however, the ecological importance of jellyfish medusae has become widely recognized. In this paper the biomass of jellyfish (medusae) in 0–60 m depths is calculated for the period 1980–2010. During this period the climate changed from cold to warm, and changes in zooplankton and fish distribution and abundance were observed. This paper discusses the less well known ecosystem component; jellyfish medusae within the Phylum Cnidaria, and their spatial and temporal variation. The long term average was ca. 9×108 kg, with some years showing biomasses in excess of 5×109 kg. The biomasses were low during 1980s, increased during 1990s, and were highest in early 2000s with a subsequent decline. The bulk of the jellyfish were observed in the central parts of the Barents Sea, which is a core area for most 0-group fishes. Jellyfish were associated with haddock in the western area, with haddock and herring in the central and coastal area, and with capelin in the northern area of the Barents Sea. The jellyfish were present in the temperature interval 1°C<T<10°C, with peak densities at ca. 5.5°C, and the greatest proportion of the jellyfish occurring between 4.0–7.0°C. It seems that the ongoing warming trend may be favourable for Barents Sea jellyfish medusae; however their biomass has showed a recent moderate decline during years with record high temperatures in the Barents Sea. Jellyfish are undoubtedly an important component of the Barents Sea ecosystem, and the data presented here represent the best summary of jellyfish biomass and distribution yet published for the region.

Historical variations in the year-class strength of beaked redfish (Sebastes mentella) in the Barents Sea

Abstract Planque, B., Johannesen, E., Drevetnyak, K. V., and Nedreaas, K. H. 2012. Historical variations in the year-class strength of beaked redfish (Sebastes mentella) in the Barents Sea. – ICES Journal of Marine Science, 69: 547–552. The present work provides the first quantitative estimate of the historical fluctuations in the year-class strength of beaked redfish in the Barents Sea. The year-class strength index is based on scientific survey data collected by Norway and Russia during the past three decades. It is defined as the effective number of 0-group fish that will eventually enter the fishery. Uncertainties in the year-class strength indices are estimated using a statistical modelling approach, which accounts for observation errors. The reconstructed series indicate clear periods of high recruitment (late 1980s–early 1990s) and 8 years of near complete recruitment failure (1996–2003). The apparent recovery in recent years is highly uncertain and needs to be confirmed by future observations. The modelling approach developed here can be applied to other fish stocks for which catch-at-age data are available from several surveys.

Thermal habitat for 0-group fish in the Barents Sea; how climate variability impacts their density, length, and geographic distribution

AbstractEriksen, E., Ingvaldsen, R., Stiansen, J. E., and Johansen, G. O. 2012. Thermal habitat for 0-group fish in the Barents Sea; how climate variability impacts their density, length, and geographic distribution. – ICES Journal of Marine Science, 69: 870–879. Between 1980 and 2008, the climate changed from cold to warm conditions in the Barents Sea. Warmer conditions have been indicated as favourable for cod, haddock, and herring recruitment and unfavourable for capelin, although during recent years these relationships have weakened and need to be revised. Extensive survey observations of temperature and 0-group cod, haddock, herring, and capelin are explored, a bounded temperature range occupied by ∼80–90% of 0-group fish (core thermal habitat, CTH) defined for each species, and an analysis made of how climate variability influenced density, length, and geographic distribution. Maximum fish densities were at 6.2°C for cod, 7.2°C for haddock, 7.0°C for herring, and 5.1°C for capelin. The area of CTH for cod, haddock, and herring increased from cold to warm years, as did the occupation area of each species. Capelin underwent a northeast distributional shift from cold to warm years. The 0-group fish were observed in a broad range of temperatures of −1 to 10.5°C. However, fish densities showed a dome-shaped distribution with temperature. Mean fish length was 7.1 cm for cod, 8.9 cm for haddock, 7.0 cm for herring, and 4.6 cm for capelin, with length distributions exhibiting a non-uniform response to temperature.

Concurrent recruitment failure in gadoids and changes in the plankton community along the Norwegian Skagerrak coast after 2002

Abstract Johannessen, T., Dahl, E., Falkenhaug, T., and Naustvoll, L. J. 2012. Concurrent recruitment failure in gadoids and changes in the plankton community of the Norwegian Skagerrak coast after 2002. – ICES Journal of Marine Science, 69: 795–801. Since 1919, annual beach-seine sampling has been carried out along the Norwegian Skagerrak coast with the main objective of measuring the abundance of 0-group gadoids. Repeated incidents of abrupt and persistent recruitment collapses in gadoid populations have been observed locally. These collapses have been linked to gradual eutrophication, which has resulted in abrupt changes in the plankton community and deprivation of adequate prey for 0-group fish. Since 2002, the recruitment of 0-group gadoids has been very poor along the Skagerrak coast on a regional scale. At the same time, major changes in the plankton community have been observed. A regular and pronounced autumn bloom dominated by red-tide forming dinoflagellates such as large Ceratium spp. and the toxic Karenia mikimotoi has practically vanished, and a linear decrease in oxygen concentration at intermediate depths (30 m) that has been evident since the 1960s, was reversed around 2002. These changes would normally indicate improved environmental conditions. However, the recruitment failure in gadoids does not support this perception. Rather, the evidence points towards a potential shift in the plankton community that has resulted in gadoid recruitment failure.

Ecological significance of 0-group fish in the Barents Sea ecosystem

Investigations into the 0-group fish in the Barents Sea have been carried out since 1965, with the goal of estimating the abundance of 0-group fish. 0-group abundance indices have been used in the assessment of the recruitment level and in recruitment variability studies. However, the ecological importance of the 0-group fish in the Barents Sea has been less studied. Although 0-group capelin, herring, cod and haddock are widely distributed in the Barents Sea, the central area seems to be the most important, accounting for approximately 50–80% of the annual biomass. The total biomass of the four most abundant 0-group fish species can be up to 3.3 million tonnes, with an average of 1.3 million tonnes (1993–2009). Wide distribution and high biomass of pelagically distributed 0-group fish make these fishes an important element in the energy transport between different trophic levels and different geographical areas, having a critical impact on the entire Barents Sea ecosystem. In recent years, capelin have shown a pronounced northward shift in biomass distribution, and several successive strong year classes occurred during warm temperature conditions. Cod biomasses were unexpectedly low during warm years and were positively correlated with spawning stock biomass, while the correlation with temperature was not significant. Haddock and herring show, as expected, increasing biomass with increased temperature when the spawning stock is at a sufficiently high level.

Role of mangroves as nurseries for French grunt Haemulon flavolineatum and schoolmaster Lutjanus apodus assessed by otolith elemental fingerprints

Juvenile French grunt Haemulon flavolineatum and schoolmaster Lutjanus apodus were captured in mangrove and seagrass stations in St. Croix, and Puerto Rico in 2006 and 2007 to deter- mine whether areas for juvenile fish can be discriminated by means of otolith chemistry. Concentra- tions of 16 elements were determined in 0-group fish otoliths using laser ablation-inductively coupled plasma mass spectrometry. Two stable isotopes, δ 18 O and δ 13 C, in French grunt and schoolmaster otoliths were also analyzed. Multi-elemental signatures for both species differed significantly (p < 0.001) among mangrove and seagrass stations within both islands. Furthermore, concentrations of 6 el- ements (Sr, Ba, Cu, Mg, Co, Na) as well as δ 18 O and δ 13 C for both species within each year differed sig- nificantly among mangrove and seagrass stations within islands (p < 0.001). Classification success for French grunt and schoolmaster juvenile areas within St. Croix across years ranged from 87 to 92% and from 76 to 77%, respectively, whereas in Puerto Rico, classification success for French grunt and schoolmaster for the 2 years ranged from 80 to 84% and 84 to 87%, respectively. Classification success between mangrove and seagrass habitats (stations combined) in Puerto Rico for French grunt ranged from 84 to 91%, and for schoolmaster ranged from 94 to 99%. In St. Croix, classification success for French grunt was 95 to 96%, and for schoolmaster was 86 to 89%. The percentages of French grunt subadults collected from forereef stations in St. Croix, identified as having resided as juveniles in man- grove habitats in 2006 and 2007, were 40 and 68%, respectively, while for Puerto Rico, these percent- ages were 70 and 74%. By contrast, for schoolmaster almost 100% of all fish in both islands resided as juveniles in mangrove habitats in both years. This study contains the first direct evidence of postsettle- ment fish movement connecting mangrove habitats to the reef using otolith chemistry.

Line transects, environmental data and GIS: Cetacean distribution, habitat and prey selection along the Barents Sea shelf edge

Cetacean observations obtained during sighting surveys for abundance estimation can also be used to investigate cetacean habitat and prey selection, the principal processes underlying cetacean distributions. In this paper, we investigate habitat and prey selection of minke (Balaenoptera acutorostrata), fin (B. physalus) and sperm (Physeter macrocephalus) whales and Lagenorhynchus (Atlantic white-sided L. acutus and white-beaked L. albirostris) dolphins observed along predetermined cruise tracks along the Barents Sea shelf edge in 2000, 2001 and 2002. The observations were combined with simultaneously collected data on habitat (depth, sea surface temperature, and temperature gradients) and prey (plankton, 0-group fish, capelin and herring) distributions in a GeographicInformation System (GIS) to investigate habitat and prey selection. Minke whales were associated with cold waters and herring, and capelin in years with low herring abundance. Fin whales were mainly associated with northern cold and deep waters, as well as capelin, 0-group fish and plankton. Lagenorhynchus dolphins were associated with capelin. Finally, sperm whales were associated with deep waters and 0-group fish. Sperm whales were probably indirectly attracted to 0-group fish through preying on predatory fish such as Sebastes spp. and the squid Gonatus spp. The cetacean species responded differently to annual variation in habitat and prey distributions. Minke and fin whale distributions and abundances remained similar between years within the study area, suggestingthat these species are generalists responding to environmental changes by switching between prey species. Conversely, Lagenorhynchus dolphins shifted northwards, likely due to tracking the shifting capelin distributions. The results are discussed in light of how such cetacean habitat and cetacean prey relationships can be valuable for the proper assessment of population sizes and trends, both through guiding the design of sighting surveys and assessing whether changes in abundances within fixed surveyed areas are due to distribution shifts or changes in population sizes.

Distribution and diet of 0-group cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) in the Barents Sea in relation to food availability and temperature

Distribution of 0-group cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) in August–September 2005 and 2006 was mainly restricted to the Atlantic waters of the western and central areas of the Barents Sea. The main distribution of 0-group fish overlapped largely with areas of high biomass (>7 gm−2 dry weight) of zooplankton. The copepod Calanus finmarchicus and krill Thysanoessa inermis, which are dominant zooplankton species in both Atlantic and boreal waters of the Barents Sea, were the main prey of 0-group cod and haddock. The main distribution, feeding areas and prey of 0-group cod and haddock overlapped, implying that competition for food may occur between the two species. However, though their diet coincided to a certain degree, haddock seems to prefer smaller and less mobile prey, such as Limacina and appendicularians. As 0-group fish increased in size, there seems to be a shift in diet, from small copepods and towards larger prey such as krill and fish. Overall, a largely pelagic feeding behaviour of 0-group cod and haddock was evident from this study.

Environmental effects on the recruitment variability of nursery species

The recruitment variability of the marine fish species Dicentrarchus labrax, Platichthys flesus and Solea solea was evaluated in the Mondego estuary (Portugal) from 2003 to 2007. The relationships between sea surface temperature, NAO index, coastal wind speed and direction, precipitation and river runoff prior to the estuarine colonization and the abundance of 0-group fish were evaluated using gamma-based Generalized Linear Models. Dicentrarchus labrax and P. flesus 0-group decreased in abundance towards the end of the study period, while S. solea, despite low abundance in 2004, increased in abundance in 2007. For D. labrax, river runoff, precipitation and east–west wind were significant; for P. flesus, precipitation, river runoff and both north–south and east–west wind components were significant parameters, while for S. solea only river runoff was important. Results were compared with recent projections for climate change scenarios, to evaluate their effects on future recruitment levels.

An Evaluation of 0-Group Abundance Indices of Barents Sea Fish Stocks

The International 0-group fish survey in the Barents Sea (1965-2002) aimed to give initial indication of the re- cruiting year class strengths. Since 2003 the 0-group survey has been a part of a Joint Norwegian-Russian ecosystem sur- vey of the Barents Sea, conducted by IMR (Norway) and PINRO (Russian Federation). The electronic 0-group databases were missing some data and contained errors, therefore the databases have been quality checked and corrected for the pe- riod 1980-2006. Two separate sets of 0- group indices were re-estimated, both with and without correction for capture ef- ficiency, using a stratified sample mean approach, and 0-group indices were correlated with other appropriate abundance indices. The exclusion of errors from the database has improved our confidence in the indices and analysis. In general, the 0-group indices seem to be reliable predictors of year class strengths and are adequate to use as input in stock assessment- models and recruitment studies.

Feeding of the Norwegian spring spawning herring Clupea harengus (Linne) at the different stages of its life cycle

Abstract The aim of the research was to investigate the diet of herring at different stages of its life cycle. For that purpose feeding of 0-group and immature herring in the Barents Sea, as well as of mature fish from the Norwegian Sea, was studied. 0-Group herring was sampled in the Barents Sea in August–September 2002–2005 during the international 0-group and trawl-acoustic survey of pelagic fish, as well as during the trawl-acoustic survey of demersal fish in November–December 2003–2004. Stomach samples of immature herring (1–3 years) were collected in late May and early of June 2001 and 2005 in the south-western part of the Barents Sea during the trawl-acoustic survey for young herring. Stomach samples of mature herring were collected in the Norwegian Sea in 1996, 1998, 1999, 2001, and 2002 in the course of the international trawl-acoustic survey of pelagic fish. Feeding intensity of herring of all age groups varied considerably between years and this was probably associated with availability and accessibility of their prey. The 0-group herring was found to have the most diverse diet, including 31 different taxa. In August–September, copepods, euphausiids, Cladocera, and larvae Bivalvia were most frequent in the diet of 0-group herring, but euphausiids and Calanus finmarchicus were the main prey taken. In November–December, euphausiids and tunicates were major prey groups. It was found that C. finmarchicus in the diet of 0-group herring was replaced by larval and adult euphausiids with increasing fish length. C. finmarchicus was the principal prey of immature herring and dominated in the diet of both small and large individuals and mainly older copepodites of C. finmarchicus were taken. Larval and adult euphausiids were found in stomachs of immature herring as well, but their share was not large. The importance of different prey for mature herring in the Norwegian Sea varied depending on the feeding area and length of the herring. On the whole C. finmarchicus and 0-group fish were the most important prey for mature herring diet, but fish prey were only important in a small sampling area. Hyperiids, euphausiids, tunicates, and pteropods were less important prey, and in 2002 herring actively consumed herring fry and redfish larvae.

Estuarine colonization, population structure and nursery functioning for 0-group sea bass (Dicentrarchus labrax), flounder (Platichthys flesus) and sole (Solea solea) in a mesotidal temperate estuary

The function of the Mondego estuary as a fish nursery habitat was investigated from June 2003 to June 2004 by comparing the timing of estuarine colonization with juveniles of sea bass Dicentrarchus labrax, flounder Platichthys flesus, and sole Solea solea, while also analysing their population structure, growth and diet composition. Differences in the onset of estuarine colonization were observed, since sole juveniles were the first to enter the estuary (in January), followed by flounder in April and sea bass in June. The estuarine population of these species consisted of several age-groups, although the majority of individuals belonged to age-groups 0 and 1. The growth rates determined for 0-group fish were within the range of those reported for other European estuarine systems. Some differences were also recognized regarding the timing of estuarine colonization and the length of the growing season. Diet of 0-group sea bass consisted mainly of Crustacea, Polychaeta and Mollusca. Flounder juveniles fed chiefly on Amphipoda (especially Corophium spp.), with Polychaeta, Isopoda and Decapoda also being common prey. The diet of 0-group sole was dominated by Polychaeta, with Amphipoda, Mollusca and Decapoda ranking highest, with other important benthic organisms also being present. Dietary overlap among these species was relatively low.

Drift probabilities for Icelandic cod larvae

AbstractBrickman, D., Marteinsdottir, G., Logemann, K., and Harms, I. H. 2007. Drift probabilities for Icelandic cod larvae – ICES Journal of Marine Science, 64, 49–59. The climatological distribution of juvenile Icelandic cod is characterized by a negative spatial age gradient, with a fairly abrupt decrease in age near the northwest corner of Iceland, and a spatial abundance gradient with higher concentrations of 0-group fish inshore. Flowfields from a high-resolution circulation model developed for Icelandic waters were used to investigate larval drift from the various spawning grounds in Icelandic coastal waters to understand the distribution of 0-group fish. To present the results clearly, drift probability density functions (pdfs) are derived describing the probability of drifting from a given spawning ground to a given spatial region over a specified time interval. These pdfs are used to determine the spawning grounds most probably contributing to the observed age distribution. The observed spatial gradient in age is likely due to differences in the spawning location of larvae, with older larvae originating in spawning grounds in the southwest and younger larvae from farther north. In general, the contribution from the main spawning grounds in the southwest is predicted to decrease with clockwise distance from the source region. The pdf technique was also used to investigate drift from regions on the south coast of Iceland corresponding to known or possible subpopulation spawning grounds, to see whether these spawning areas are associated with distinct drift patterns. This technique is a useful way to present larval drift results and to facilitate comparison with real data.

Enhanced survival of 0-group gadoid fish under jellyfish umbrellas

Young (0-group) gadoid fish, which have been observed sheltering beneath jellyfish (Scyphozoa and Hydrozoa) umbrellas, may find refugia from predation by retreating among medusan tentacles. The survival of juvenile gadoids may therefore be improved by high abundances of medusae. Jellyfish (including Cyanea lamarckii and C. capillata) were caught in the North Sea during routine sampling for 0-group gadoids (cod Gadusmorhua, haddock Melanogrammus aeglefinus, Norway pout Trisopterus esmarkii and whiting Merlangius merlangus) between 1971 and 1986, and considerable overlaps have been shown between the spatial distributions of these fish and medusae. Here correlations are made between the abundance of medusae in the North Sea and the residual survival of 0-group fish, as quantified by the deviation in 1-group recruitment from the expected Ricker modelled estimate. Significant positive correlations between the residual survival of whiting and medusa abundance are evident for each individual Cyanea sp. and for the combined Cyanea spp. ln(maximum) abundance (all R ≥ 0.60, P < 0.01, N = 15). The abundance of jellyfish may thus be an important factor influencing the mortality of whiting in the North Sea, and as such should be considered in the development of ‘ecosystem-based’ management of whiting stocks.