Status,number, and monitoring of the common eider (<Emphasis Type="Italic">Somateria mollissima</Emphasis>) population in the barents sea and the White Sea

The breeding, molting, and wintering ranges of the common eider (Somateria mollissima) were mapped and described in the southern part of the Barents Sea region, including the White Sea population in the western White Sea and the Murmansk population in the northwestern White Sea and the southeastern Barents Sea. The present-day abundance was determined for both populations: since the 1950s, it was the highest in the 2000s for the entire period of ornithological monitoring in the region. Aerial survey from a helicopter is considered to be the only reliable method for estimation of the total population number. The best season for surveying the White Sea population is March–early April (wintering); the most favorable period for surveying the Murmansk population is August (postbreeding/molting). The population status of the common eider in the northern and eastern parts of the Barents Sea has not yet been evaluated. On Franz-Josef Land, the common eider is distributed sporadically, and its number was assessed using expert estimates. The current abundance of the common eider on Novaya Zemlya is unknown. Helicopter-based aerial survey performed in late summer during the postbreeding season is the only relevant method to obtain reliable estimates for the population of the common eider inhabiting Franz-Josef Land and Novaya Zemlya.     

Structure and specific features of formation of aggregations of deepwater redfish <Emphasis Type="Italic">Sebastes mentella</Emphasis> (Scorpaenidae) in the Norwegian Sea pelagial

Results of studies of the structure and specific features of formation of aggregations of deepwater redfish Sebastes mentella in the Norwegian Sea pelagial are provided. Data on the biological characteristics of S. mentella from different regions of the Norwegian Sea pelagial do not allow us to consider its aggregations as separate populations. On the basis of comparative analysis of the structure of aggregations in the Norwegian Sea and of population parameters and specific features of the life cycle of S. mentella in different parts of the Atlantic Ocean, its complex intraspecies organization at sites of overlapping of two largest populations—North Atlantic and Norwegian-Barents Sea-was established. The formation of pelagic aggregations in the water area of the Norwegian Sea occurs due to migration of maturing and mature individuals from the adjoining water areas. In the southern areas of the Norwegian Sea, dominant recruitment comes from the pelagial of the northeastern part of the Irminger Sea, which is promoted by the direction of streams of the North-Atlantic Current; it is not excluded either that fish can migrate to the southern part of the sea from the slopes of the Faeroes, Faeroes-Icelandic threshold, and the western coast of Norway. Migration to the northern areas of the sea is mainly performed by rapidly maturing fish from the rearing region from the western slopes of the Barents Sea and Spitsbergen Archipelago. The presence of seasonal migrations hinders the formation in the pelagial of perch isolated groups and promotes their migration.     

New Data on the Distribution of Lamprey <Emphasis Type="Italic">Petromyzon marinus</Emphasis> and <Emphasis Type="Italic">Lethenteron camtschaticum</Emphasis> (Petromyzontidae) in Barents and White Seas

Information about the sites of catches of the sea lamprey Petromyzon marinus in the western Barents Sea and Arctic lamprey Lethenteron camtschaticum in the Barents and White seas is presented based on the data of trawl surveys performed in 2004?2016. It is demonstrated that sea lamprey is occasionally encountered in the western Barents Sea; nine specimens have been recorded during the entire period of surveys. The northernmost point of a capture of sea lamprey is located near 76° N and the easternmost point is at 31°15′ E. Arctic lamprey is not numerous in the Barents and White seas; a total of 66 and 17 specimens have been caught, respectively. Its local aggregations are found in the southeastern part of the Barents Sea and in Dvina Bay in the White Sea. Arctic lamprey penetrates to the north to 76° N and into the central part of the Barents Sea.     

An analysis of allozyme variation in herring <Emphasis Type="Italic">Clupea pallasii</Emphasis> from the White and Barents Seas

An analysis of genetic variation is made according to four allozyme loci of reproductive (spawning) groups of oligovertebrate herring Clupea pallasii collected in various bays of the White Sea and the south-eastern part of the Barents Sea in 1995–2002. The temporal stability of genetic characteristics during several years is shown. The analysis of genetic variation revealed a significant difference between herring from the south-eastern part of the Barents Sea and spring-spawning and summer-spawning herring from inner bays of the White Sea. The analysis of geographic variation of genetic characteristics of spawning aggregations revealed the change in frequencies of alleles of loci LDH-2* and MDH-4* from the north-east to the south-west along the coast.     

Intraspecific variability in the “vowel”‐like sounds of beluga whales (Delphinapterus leucas): Intra‐ and interpopulation comparisons

The beluga whale (Delphinapterus leucas) has a rich and complicated vocal repertoire. However, different populations use similar and common types of signals. We studied physical features of one of these types, “vowels,” in three Russian populations: the White Sea population (European North), the Chukotka population (the Bering Sea, Chukotka), and the Okhotsk Sea population (Russian Far East) as well as in four summer aggregations of the White Sea belugas over several years in duration. The pulse repetition rate (PRR) at half of the duration of the signal was measured. We found that the PRR of “vowels” collected in the same summer aggregation during different years is stable in time but varies between locations. The degree of variation corresponds with the geographic distance between different locations. Significant differences were discovered between populations separated by thousands of kilometers, and to a lesser extent, between summer aggregations inhabiting different bays of the White Sea. The variation in PRR between the locations can be caused by the divergence of signals owing to the accumulation of random errors during transmission of these signals from generation to generation, which progressed independently in different summer aggregations and populations.     

Intraspecies structure of beaked redfish <Emphasis Type="Italic">Sebastes mentella</Emphasis> of the Atlantic and Arctic oceans

On the basis of the results of complex interdisciplinary investigations of the population composition and structure of the beaked redfish Sebastes mentella of the Atlantic and Arctic oceans, its three populations are discerned relatively isolated from each other by the system of permanent marine currents—North Atlantic, Flemish-Cape, and Norway-Barents Sea. The population structure of the species in the southern part of its area corresponds to the model of a local stock. Interaction of the North Atlantic and the Norway-Barents Sea populations well correspond to the model of fluctuating stocks. Redfish aggregations in different biotopes (mesobenthal and mesopelagial) are intrapopulational epigenetic groups. In the period of warm and anomalously warm years, a part of mature specimens from the pelagial of the North Irminger Sea make an irreversible migration to the southern part of the Norwegian Sea and form there mixed aggregations of fish from the North Atlantic and Norway-Barents Sea populations. With consideration of the effect of climatic–oceanological processes, a principally new scheme is elaborated describing the process of seasonal migrations of redfish in the mesobenthal and mesopelagial. The previous views on direction of return migrations of redfish of the Norway-Barents Sea population are reconsidered. Juveniles from the western part of the Barents Sea and Spitsbergen not only supplement the demersal aggregations but also migrate to the pelagial of the Norwegian Sea.     

Seasonal distribution and dive behaviour of harp seals (<Emphasis Type="Italic">Pagophilus groenlandicus</Emphasis>) of the White Sea–Barents Sea stock

Eight adult female harp seals (Pagophilus groenlandicus) of the White Sea–Barents Sea stock were tagged with satellite-linked dive recorders during the nursing period and followed from breeding in late February 1995 until moulting in late April 1995. Another ten adult harp seals of both sexes were tagged and followed from moult in early May 1996 until breeding in late February the following year. Between breeding and moult the seals were distributed along the coasts of Kola of Russia and eastern Finnmark of Norway, coinciding in time and space with the spawning capelin (Mallotus villosus). Between moulting and breeding they encircled the entire Barents Sea, mostly in open water, using the water column from 20 to 300 m, and in so doing by and large reflecting the annual migrations of the capelin. Capelin is therefore assumed to be the main source of prey for the White Sea–Barents Sea stock of harp seals, to be substituted, in part, by amphipods (e.g. Themisto libellula) in mid-summer and polar cod (Boreogadus saida) and herring (Clupea pallasii) in late autumn and winter. These data provide a baseline for the evaluation of the effects of future climatic change in the rich Barents Sea ecosystem.     

Panmictic population structure in the hooded seal (Cystophora cristata)

Two putative populations of hooded seals (Cystophora cristata) occur in the North Atlantic. The Greenland Sea population pup and breed on the pack ice near Jan Mayen ('West Ice') while the Northwest Atlantic population is thought to pup in the Davis Strait, in the Gulf of St. Lawrence (the 'Gulf'), and off southern Labrador or northeast Newfoundland (the 'Front'). We used microsatellite profiling of 300 individuals at 13 loci and mitochondrial DNA sequencing of the control region of 123 individuals to test for genetic differentiation between these four breeding herds. We found no significant genetic differences between breeding areas, nor evidence for cryptic nor higher level genetic structure in this species. The Greenland Sea breeding herd was genetically most distant from the Northwest Atlantic breeding areas; however, the differences were statistically nonsignificant. Our data therefore suggest that the world's hooded seals comprise a single panmictic genetic population.     

Harp seal foraging behaviour during summer around Svalbard in the northern Barents Sea: diet composition and the selection of prey

The harp seal Pagophilus groenlandicus is a major high trophic level predator in the Barents Sea, and to better understand their function in the Barents Sea ecosystem, we need to understand their foraging behaviour during their most intensive feeding period. We analysed the diet composition and prey preference of 184 harp seals and 94 faeces samples, sampled in the northern Barents Sea (around Svalbard) during the period May–August in 1996, 1997, and 2004–2006. Concurrent with the sampling of seals, prey availability was assessed in one area in 1996 and 1997 and in two areas in 2006 using standard acoustic methods. Our study showed that harp seal diet composition varied significantly both in time (year) and space, and that their diets appeared to be size dependent. Both subadult (<150 cm) and adult seals were associated with pelagic crustaceans (particularly krill), whereas primarily adult seals were associated with fish (capelin, gadoids and flatfish). Krill was the most important prey group (63 %) followed by polar cod (16 %) and other fish species (10 %). The prey preference of harp seals varied in time and space; polar cod was often preferred by the seals whereas krill was commonly consumed in lower proportion than observed in the survey area. Gadoids and capelin had either been exploited in the same or less proportion as observed in the survey sea. This study emphasises the ecological significance of krill as prime food for harp seals during their intensive feeding period in summer.     

On the spatial relationship between the spawning and feeding parts of the range of lumpfish Cyclopterus lumpus (Cyclopteridae) in the Barents Sea and adjacent waters (according to results of analysis of the size composition similarity)

Results of analysis of similarity of size series of mature females of the lumpfish Cyclopterus lumpus collected on the spawning grounds in the Barents and Norwegian seas (Russian and Norwegian coasts), as well as in the areas of its feeding, are provided. The trajectories of feeding migrations of lumpfish in the southern part of the Barents Sea have been revealed. A clinal decrease in the average length of females in the range from west to east is shown. The area of feeding aggregations of lumpfish spawning off the Russian coast is distinguished. The boundaries of the census water area used to assess the commercial stock of lumpfish and to determine the values of its possible catch off the coast of Murmansk are specified.     

Mitochondrial DNA polymorphism of atlantic cod of the Barents and White seas

High level of intraspecific polymorphism of the mtDNA cytochrome b gene in the Atlantic cod Gadus morhua L. from the northeastern part of the species range (Barents and White seas) is detected. The absence of genetic differentiation between the samples from different areas of the Norwegian and Barents seas is shown, and the fact that these samples belong to the same population of Northeast Arctic cod is confirmed. Significant differences in the frequences of mitochondrial DNA haplotypes between the cod from the Barents and White seas, as well as from the northwestern part of the range, are found. The cod Gadus morhua kildinensis Derjugin, 1920 from Mogilnoye Lake and Gadus morhua marisalbi Derjugin, 1920 from the White Sea were revealed to have common haplotypes with the cod from the Barents Sea, confirming the recent origin of these forms from the Atlantic cod G. morhua.     

On the distribution of larvae and localization of spawning stocks of White Sea herring <Emphasis Type="Italic">Clupea pallasii marisalbi</Emphasis>

On the basis of ichthyoplankton surveys made in June 2004–2005 and 2007, June–July 2010, and July 2011 in these bays and beyond them (in open waters of the White Sea Basin and adjacent areas of the Gorlo) larvae of White Sea herring were absent. Principal aggregations of larvae are found in the Kandalaksha Bay in June 2004–2005 and 2007. In the Onega Bay and in the Dvina Bay surveyed in June 2007 abundance of larvae was ratter low and in June–July 2010 and July 2011 in these bays and beyond them (in open waters of the White Sea Basin and adjacent areas of the Gorlo) larvae of White Sea herring were absent. Within the Kandalasksha Bay, from year to year, there were two disconnected aggregations of larvae. The space between them was situated in the open part of the bay along the transect of the Chupa Estuary and the Umba Estuary. One of the aggregations of larvae occupied the tail of the bay, and the second aggregation occupied the ante-mouth and mouth areas of the Chupa Estuary. It is supposed that these aggregations result from spawning of two independent spawning groups of the White Sea herring spawning in isolated regions of the Kandalaksha Bay. Presence of the bulk of larvae of the White Sea herring within the limits of the Kandakaksha Bay and their almost complete absence at the boundary of the bay with the White Sea Basin and at the boundaries between the Onega Bay and the Dvina Bay and the Basin support the hypothesis on the absence of an exchange with larvae between stocks of the White Sea herring spawning in large bays of the White Sea. The larvae are retained within shallow waters of the Kandalaksha Bay by the system of two-layer water circulation in the areas of spawning of herring in bays and gulfs of the estuarine type. Their drift outside of the Onega Bay and the Dvina Bay may be delimited by frontal divides at their boundaries with the Basin.     

Trophic level and fatty acids in harp seals compared with common minke whales in the Barents Sea

The objectives of this study were to explore trophic levels and possible diet overlap between harp seals (Pagophilus groenlandicus) and common minke whales (Balaenoptera acutoroostrata) in the Barents Sea using stable isotopes of nitrogen (δ¹⁵N) and carbon (δ¹³C) and fatty acid analyses, and to explore the energy pathways from the plankton to the top predators. Blubber and muscle samples from 93 harp seals and 20 minke whales were collected in the southern Barents Sea in May 2011. The study showed that harp seals were at a higher trophic level than minke whales during spring. This supported previous diet studies suggesting a more fish-dominant diet for seals, as compared with the whales, at this time of the year. The stable isotopes and fatty acids indicated niche separation between the seals and the whales, and between different age groups of the harp seals. Older seals had fatty acid profiles more equal to minke whales as compared with younger seals. Furthermore, while the fatty acid profiles suggested that krill were of particular importance for the young seals, the profiles from older seals and whales suggested that fish dominated their diets.     

Brucella sp. antibodies in polar bears from Svalbard and the Barents Sea

A prevalence of 5.4% of anti-Brucella sp. antibodies was found in plasma samples from 297 polar bears (Ursus maritimus) from Svalbard and the Barents Sea. Plasma was tested by the classical brucellosis tests Slow Agglutination of Wright (SAW), EDTA modified SAW and Rose Bengal test, as well as by an indirect Protein A ELISA. Only samples classified as positive in all tests were regarded as containing anti-Brucella sp. antibodies. A significant west to east increase in the proportion of bears with anti-Brucella sp. antibodies was found, with 3.6% (n = 253) at Svalbard (Spitsbergen, Nordaustlandet, Edge?ya, Barents?ya and Hopen), and 15.9% (n = 44) in the central Barents Sea. Anti-Brucella sp. antibodies were previously found in ringed seals (Phoca hispida) and harp seals (Phoca groenlandica) from the same geographical areas. The ringed seal is an important prey species for the Svalbard polar bear population, and may thus be a source of brucellosis for the bears. There are no indications of reproductive disorders caused by Brucella sp. or other infectious agents in our study polar bear population. Potential impacts of Brucella sp. exposure on individuals or the population are unknown.     

DIET OF WEANED PUPS AND SEASONAL VARIATIONS IN BODY CONDITION OF JUVENILE BARENTS SEA HARP SEALS PHOCA GROENLANDICA

Data on blubber depth, body condition, and diet were collected from young of year and juvenile harp seals ( Phoca groenlandica ) in the Barents Sea in the periods February-April and June-October 1990–1997. Harp seal pups feed independently shortly after weaning. In the southern parts of the Barents Sea the diet of harp seal pups consisted mainly of euphausiids ("krill") Thysanoessa sp. and amphipods of the genus Parathemisto . The change in body condition of harp seal pups between weaning (mid-March) and June indicated that considerable amounts of blubber energy, deposited during suckling, were mobilized. This suggests that the early food intake of weaned pups was insufficient to meet the energy requirements. The pattern of low spring and earlysummer body condition, followed by a subsequent rapid improvement in condition during late summer and autumn appeared to occur not only among pups-of-the-year, but also in one- and two-year old harp seals.     

Diet composition of polar bears in Svalbard and the western Barents Sea

We estimated both the numerical and biomass composition of the prey of polar bears (Ursus maritimus) from 135 opportunistic observations of kills in Svalbard and the western Barents Sea collected from March to October 1984-2001. By number, the prey composition was dominated by ringed seals (Phoca hispida) (63%), followed by bearded seals (Erignathus barbatus) (13%), harp seals (P. groenlandica) (8%) and unknown species (16%). However, when known prey were converted to biomass, the composition was dominated by bearded seals (55%), followed by ringed seals (30%) and harp seals (15%). Results indicated that bearded seals are an important dietary item for polar bears in the western Barents Sea. We believe that different patterns of space use by different bears may result in geographic variation of diet within the same population.     

Feeding habits of harp seals (Phoca groenlandica) during early summer and autumn in the northern Barents Sea

The feeding habits of harp seals (Phoca groenlandica) in the Barents Sea were examined in studies conducted during June 1991, September 1990 and 1991, and October 1992. Analyses of stomach and intestinal contents were carried out and concurrent estimates of prey abundance were made using trawl gear. Harp seals appeared to feed at low intensity in the pack ice belt during the first half of June. There was little potential prey in the water column, but prawns (Pandalus borealis), capelin (Mallotus villosus) and polar cod (Boreogadus saida) were abundant close to the bottom. In September, the seals sampled in the northern pack ice areas of the Barents Sea fed on the pelagic amphipod Parathemisto libellula, krill (Thysanoessa spp.), prawns and, to a lesser extent, on fish species such as polar cod, sculpins (Cottidae) and snailfish (Liparidae). Trawling revealed that large quantities of Parathemisto libellala were present in the upper layers of the water column. Fish, mainly capelin and polar cod, were less abundant and occurred in deeper waters. In mid-October, the diet of seals in the northern Barents Sea consisted mainly of amphipods (Parathemisto sp.). Later in October, when increasing pack ice cover forced the harp seals to move south, the diet seemed to change from amphipods to fish prey, predominantly capelin and polar cod.     

The contribution of single and colonial cells of Phaeocystis pouchetii to spring and summer blooms in the north-eastern North Atlantic

Studies of the phytoplankton ecology in different localities in north-Norwegian fjords, the White Sea and the Barents Sea were carried out in spring and early summer to investigate the contribution of single and colonial stages of Phaeocystis pouchetii to phytoplankton abundance. Three different types of flagellated and four colonial cells were observed in all localities. P. pouchetii was rare under the ice of the Barents and White Seas, but their abundance increased rapidly during ice retreat. Single cell C dominated over colonial cell C, often by 50 times or more. The highest share of colonial cells was encountered in April in northern Norwegian fjords, in May in the Barents Sea and in May–June in the White Sea. At times the single cell dominated the total P. pouchetii biomass in Balsfjord (April 1999, 2001) with hardly any colonies present. In the White Sea colonies of P. pouchetii were less abundant than in the other regions. Cell carbon of P. pouchetii colonies appears never to be as dominating in the north-eastern North Atlantic as P. globosa blooms in coastal regions such as the southern North Sea. However, the lobal matrix of P. pouchetii colonies appears to be less solid than that of P. globosa and partly dissolution of the colony matrix during handling and storage of fixes samples induces uncertainty about the absolute numbers of P. pouchetii colonial cell counts. Despite of that, single cells of P. pouchetii seem to dominate significantly over colonial cell biomass at most sites and during some years and in some regions colonial cells seem rare. We speculate that top-down regulation of Phaeocystis spp. blooms possibly determines the ratio between single and colonial cells.     

Spatial structure in length at age of cod in the Barents Sea

Cod Gadus morhua population in the Barents Sea was found to be spatially structured with regard to length-at-age. Results were based on data collected during research surveys in the Barents Sea between 1982 and 1997. The identified spatial structure was most pronounced for age groups 2–4 years and decreased for the older age groups with higher potential for migration. A positive linear correlation between mean length-at-age and mean geographical temperature was established for age groups 2–4 years. This correlation was shown to be strongest when based on mean temperatures during 3 year periods ending with the year of capture. The spatial structure in length-at-age was shown to follow the temperature gradient of the Barents Sea. A large part of the observed area effects could be explained by temperature variation between areas. Evidence is also presented which indicates that the predictability and sensitivity of the dependence of length-at-age on temperature increases under extreme environmental conditions, i.e. in the northern and eastern areas of the Barents Sea.     

Subtidal populations of the blue mussel <Emphasis Type="Italic">Mytilus edulis</Emphasis> as key determinants of waterfowl flocks in the southeastern Barents Sea

Ornithological surveys conducted over the Pechora Sea (the southeastern part of the Barents Sea) in the 1990 s revealed huge non-nesting flocks of marine ducks, the largest in the European North. Especially dense waterfowl aggregations are constantly observed at the shallows near Dolgij Island during molting period and migration to wintering places. All the marine ducks flocking there are specialized benthos feeders predominantly consuming mussels Mytilus edulis. At the same time, numerous previous benthic studies in the Pechora Sea did not reveal mussels near Dolgij Island where benthic biomass was somewhat lower than in the adjacent areas (Denisenko in Mar Ecol Prog Ser 258:109–123. 2003) which left the food source for these abundant bird flocks enigmatic. In the course of an expedition in summer 2007 we found subtidal populations of M. edulis in shallows to the southwest of Dolgij Island. These populations were confined to a coastal zone and were characterized by a highly disjunct distribution with the biomass reaching up to 4 kg m⁻². We describe these subtidal populations as well as an intertidal mussel population on the western shore of Dolgij Island.