The Bowhead Whale, <Emphasis Type="Italic">Balaena mysticetus</Emphasis> Linnaeus, 1758, in the Western Sea of Okhotsk (2009–2016): Distribution Pattern,Behavior, and Threats

The data on sightings of the bowhead whale (Balaena mysticetus Linnaeus, 1758) in the western Sea of Okhotsk collected during eight field seasons, as well as information obtained from interviews with local residents in the study region, are presented. The major areas of concentration of the bowhead whale population in the ice-free period are determined; the whale behavior in bays is described. Data on sea surface temperature, salinity, and depth measurements at the sites of bowhead whale sightings are provided. The possible causes of whale concentrations close to the shoreline and in apical parts of mainland shallow-water bays, as well as the potential threats to the population associated, inter alia, with this pattern of distribution, are discussed.     

Abundance estimate of the Okhotsk Sea population of the bowhead whale (<Emphasis Type="Italic">Balaena mysticetus</Emphasis> Linnaeus, 1758)

Abundance of 388 ± 108 whales for the Okhotsk Sea bowhead whale population based on individual genotyping was estimated using the capture–recapture method for the open population model. The data demonstrate that this endangered population shows no signs of recovery.     

Presence and behavior of bowhead whales (Balaena mysticetus) in the Alaskan Beaufort Sea in July 2011

The Western Arctic bowhead whale (Balaena mysticetus) is highly adapted to sea ice and annually migrates through the Bering, Chukchi, and Beaufort seas. While the overall distribution and seasonal movements of bowhead whales are mostly understood, information about their distribution in the Alaskan Beaufort Sea in early to mid-summer has not been well documented. In July 2011, we conducted an exploratory flight in the Alaskan Beaufort Sea, north of Camden Bay (71°N 144°W), near the location of a single satellite-tagged bowhead whale. Eighteen bowhead whales were observed, and behavior consistent with feeding was documented. To our knowledge, this is the first documentation of behavior consistent with feeding north of Camden Bay in mid-July. Few studies have focused on bowhead whale distribution in the Alaskan Beaufort Sea in early to mid-summer, and no long-term, region-wide surveys have been conducted during summer. Bowhead whales are already exposed to anthropogenic disturbance in the Canadian Beaufort Sea in summer, the Alaskan Beaufort Sea in fall, and the Chukchi and Bering seas from fall through spring. The presence of bowhead whale aggregations in the Alaskan Beaufort Sea in summer should be considered when assessing the cumulative effects of human-related activities.     

Epidermal Molting in the Bowhead Whale <Emphasis Type="Italic">Balaena mysticetus</Emphasis>

Epidermal molting in the bowhead whales that regularly enter Ulbanskiy Bay of the Sea of Okhotsk in summer has been reported and proven by histological methods. Longitudinal delamination and detachment of thin or thick sheets of a considerable area have been established for the surface layer (stratum externum) of the whale epidermis during molting. A correlation of molting intensity to the level of proliferation and regeneration of all epidermal layers has been noted and assumed to stabilize the thickness of the skin. The phenomenon of molting is discussed from the viewpoint of adaptation of the whales to the conditions of the shallow bays of the Sea of Okhotsk that warm up thoroughly in the summer.     

Summer molting of bowhead whales <Emphasis Type="Italic">Balaena mysticetus</Emphasis> Linnaeus, 1758, of the Okhotsk Sea population

In bowhead whales summering in Ulbanskiy Bay of the Okhotsk Sea, molting of epidermis has been found and histologically confirmed. The outer layer of the molting whale epidermis is longitudinally stratified and rejected in the form of relatively large plates up to several millimeters thick, each representing a lamellar formation consisting of longitudinal rows of parakeratocytes with degenerated nuclei, numerous pigment granules, and lipid inclusions. Molting intensity is correlated with the level of proliferation and regeneration of all epidermal layers, which helps to maintain the optimal skin thickness.     

Serological Detection of Causative Agents of Infectious and Invasive Diseases in the Beluga Whale <Emphasis Type="Italic">Delphinapterus leucas</Emphasis> (Pallas, 1776) (Cetacea: Monodontidae) from Sakhalinsky Bay

Serological detection of some pathogens in the beluga whale Delphinapterus leucas population from Sakhalinsky Bay of the Sea of Okhotsk (Sakhalin–Amur beluga whale stock) was performed in 2013–2014 after the largest recorded flood of the Amur River (among observations since 1896). The percent of this population that is immune to the causative agents of clonorchosis was 25.6%; toxoplasmosis, 11.5%; brucellosis, 38.5%; tuberculosis, 30.8%; cetacean morbillivirus infection, 16.7%; and to alpha and gamma herpes viruses each, 21.8%.     

Stomach contents of bowhead whales (Balaena mysticetus) from four locations in the Canadian Arctic

The stomach contents of four bowhead whales (Balaena mysticetus) harvested between 1994 and 2008 from the Canadian Arctic were examined to assess diet composition. Three samples were collected from bowhead whales of the Eastern Canada–West Greenland (EC–WG) population and represent, according to our knowledge, the first diet analysis from this bowhead whale stock. We also examined the stomach content of one bowhead whale from the Bering-Chukchi-Beaufort (BCB) population hunted in 1996. All four whales had food in their stomachs and their diet varied from exclusively pelagic (BCB whale), with Limnocalanus macrurus being the main prey, to epibenthic and benthic (EC–WG) with Mysis oculata playing an important role. These results indicate broad foraging spectrum of the bowhead whales and add to a basic knowledge of their diet.     

The distribution of zooplankton and bowhead whales, <Emphasis Type="Italic">Balaena mysticetus</Emphasis> Linnaeus, 1758, in Akademiya Bay,Sea of Okhotsk

The modern pattern of distribution and feeding habits of the bowhead whale, Balaena mysticetus, in the Sea of Okhotsk are studied. The existence of a feeding aggregation of this whale species in the southwesternmost portion (apex) of Ulban Bay has been confirmed. There, the animals feed in shallow waters with depths of 3–5 m, which are only slightly larger than their body height. The quantitative composition and species structure of zooplankton at the stations that were set near feeding whales have been analyzed. In the samples taken in the immediate proximity to the feeding whales, the abundance of zooplankton reached 31409 ind./m³, with the average value of 17565 ind./m³. The lowest abundance, from 56 to 1879 ind./m³ (mean 927 ind./m³), was in the samples from western Konstantin Bay, where bowhead whales were not observed. In 16 samples collected in the immediate proximity to the feeding whales in the shallow waters of Ulban Bay, the average zooplankton biomass was 547.9 mg/m³, which is 3.9 times higher than that in the samples from waters where the whales were absent. Copepods dominated quantitatively at all the stations in Akademiya Bay. The proportion of euphausiids in the zooplankton biomass was lower than 1%, both near the feeding whales and in the absence of whales.     

Occurrence of killer whale Orcinus orca rake marks on Eastern Canada-West Greenland bowhead whales Balaena mysticetus

Killer whales (Orcinus orca) are increasing in occurrence and residence time in the eastern Canadian Arctic (ECA) in part due to a decrease in sea ice associated with global climate change. Killer whales prey on bowhead whales (Balaena mysticetus) of the Eastern Canada-West Greenland (EC-WG) population, but their patterns of predation pressure and effect on the EC-WG population’s ability to recover from historical whaling remain unknown. We analyzed photographs of individual bowhead whale flukes from five regions within the EC-WG population’s geographic range (Cumberland Sound, Foxe Basin, Isabella Bay, Repulse Bay and Disko Bay), taken during 1986 and from 2007 to 2012, to estimate the occurrence of rake marks (parallel scars caused by killer whale teeth). Of 598 identified whales, 10.2 % bore rake marks from killer whales. A higher occurrence of rake marks was found in Repulse and Disko Bays, where primarily adult bowhead whales occur seasonally, than in Foxe Basin, where juveniles and females with calves occur. Older bowheads, which have had greater exposure time to killer whales due to their age, had higher occurrences of rake marks than juveniles and calves, which may indicate that younger whales do not survive killer whale attacks. A high proportion of adult females also had rake marks, perhaps due to protecting their calves from killer whale predation. In order to quantify the effect of killer whales on EC-WG population recovery, further research is needed on the relationship between the occurrence of rake marks and bowhead adult, calf, and juvenile mortality in the ECA, as well as more information about Arctic killer whale ecology.     

Estimation of the Consumption of Nekton and Plankton by the Minke Whale Balaenoptera acutorostrata

This is a review of the data available on the population subdivision and life cycle of the Minke whale, the most abundant whalebone whale in the World Ocean. Different methods of estimation and calculation of the rate of food consumption by this species, the latter including those developed for the Sea of Okhotsk, are compared.     

A genetic analysis of the beluga whale Delphinapterus leucas (Cetacea: Monodontidae) from summer aggregations in the Russian Far East

The genetic structure of four summer aggregations of the Beluga Whale, Delphinapterus leucas, in Sakhalin Bay and Udskaya Bay, off the western coast of Kamchatka in the Sea of Okhotsk and in the Anadyr Estuary of the Bering Sea was analyzed through nucleotide sequencing of the mtDNA control region and detection of the allelic composition of nine microsatellite loci in nuclear DNA. It has been shown that each of the aggregations features a unique set of maternal lines, which indicates a high degree of philopatry in this species. Beluga whales of the Anadyr Estuary are genetically isolated from those of the Sea of Okhotsk. Beluga whales of the summer aggregations of Sakhalin Bay and those from Udskaya Bay share a common gene pool and belong to a single population, while the whales that summer off western Kamchatka with great consistency may be attributed to a different population. Comparison of nucleotide sequences of the mtDNA in beluga whales from various waters of the Russian Far East and North America allowed us to propose a hypothesis about how the structure of beluga whale populations formed in the North Pacific during the postglacial period.     

Examination of ten thousand years of mitochondrial DNA diversity and population demographics in bowhead whales (Balaena mysticetus) of the Central Canadian Arctic

Mitochondrial DNA (mtDNA) sequences were analyzed from 106 bowhead whale (Balaena mysticetus) specimens dating 471 ± 44 ¹⁴C b.p. –10,290 ± 150 ¹⁴C b.p. to evaluate whether historical changes in distribution and connectivity were detectable in levels of diversity and population structuring in the Central Canadian Arctic. The species has maintained levels of mtDNA diversity over 10,000 yr comparable to other nonbottlenecked large whale species. When compared to data from the Holocene East Greenland/Spitsbergen and contemporary Bering‐Chuckchi‐Beaufort populations, differentiation was low (F_ST≤ 0.005, Φ_ST≤ 0.003) and no temporal or geographical genetic structuring was evident. A combination of analyses suggests that the population has expanded over the past 30,000 ¹⁴C yr. This genetic signature of expansion could result from population growth, admixture of multiple gene pools, or a combination of both scenarios. Despite known climatic change that altered bowhead distribution and led to isolation of populations, there is no detectable population structuring or change in genetic diversity during the Holocene. This may be due to long generation time, occasional population connectivity and a historically large global population. These characteristics warrant caution when interpreting contemporary bowhead whale DNA data, as it is unlikely that any population will be in mutation‐drift equilibrium.     

A bowhead whale in the eastern North Pacific

Bowhead whales occur in the Arctic year‐round. Their movements are largely correlated with seasonal expansions and reductions of sea ice, but a few recent extralimital sightings have occurred in the eastern and western North Atlantic and one was also documented in the western North Pacific over 50 years ago. Here we present details of a juvenile bowhead whale that was photographed and filmed from above and below the water while it was skim‐feeding in Caamaño Sound, BC, Canada on May 31, 2016. This sighting occurred over 2000 km southeast from the nearest known range for this species in the Bering Sea at a time that most bowhead whales in that region would have been migrating northeast. This sighting represents the first and only documentation of a bowhead whale in the eastern North Pacific to date.     

Characterization of 25 microsatellite loci in bowhead whales (Balaena mysticetus)

Bowhead whales (Balaena mysticetus) experienced a severe demographic population bottleneck caused by commercial whaling that ceased in 1914. Aboriginal subsistence whale harvests have continued and are managed by the International Whaling Commission. In an effort to provide management advice for bowhead whales, 25 microsatellite loci were isolated from genomic DNA libraries. This panel of markers will be utilized to analyse stock structure hypotheses of current bowhead whale populations.     

Fatty acid‐based diet estimates suggest ringed seal remain the main prey of southern Beaufort Sea polar bears despite recent use of onshore food resources

Polar bears (Ursus maritimus) from the southern Beaufort Sea (SB) subpopulation have traditionally fed predominantly upon ice‐seals; however, as the proportion of the subpopulation using onshore habitat has recently increased, foraging on land‐based resources, including remains of subsistence‐harvested bowhead whales (Balaena mysticetus) and colonial nesting seabirds has been observed. Adipose tissue samples were collected from this subpopulation during the springs of 2013–2016 and analyzed for fatty acid signatures. Diet estimates were generated for the proportional consumption of ringed seal (Pusa hispida), bearded seal (Erignathus barbatus), and beluga whale (Delphinapterus leucas), relative to onshore foods, including bowhead whale remains and seabird, as represented by black guillemot (Cepphus grylle mandtii) nestlings and eggs. Quantitative fatty acid signature analysis (QFASA) estimated that the ice‐obligate prey, ringed seal, remained the predominant prey species of SB polar bears (46.4 ± 1.8%), with much lower consumption of bearded seal (19.6 ± 2.0%), seabird (17.0 ± 1.2%), bowhead whale (15.0 ± 1.4%), and hardly any beluga whale (2.0 ± 0.5%). Adult and subadult females appeared to depend more on the traditional ringed seal prey than adult and subadult males. Diet estimates of SB polar bears showed significant interannual variability for all prey (F_{12, 456} = 3.17, p < .001). Longer‐term estimates suggested that both types of onshore prey, bowhead whale remains and seabird, have represented a moderate proportion of the food resources used by SB polar bears since at least the start of the 21st Century.     

Song sharing and diversity in the Bering‐Chukchi‐Beaufort population of bowhead whales (Balaena mysticetus), spring 2011

Bowhead whales (Balaena mysticetus) of the Bering‐Chukchi‐Beaufort population migrate in nearshore leads through the Chukchi Sea each spring to summering grounds in the Beaufort Sea. As part of a population abundance study, hydrophones were deployed in the Chukchi Sea off Point Barrow, (12 April to 27 May 2011) and in the Beaufort Sea (12 April to 30 June 2011). Data from these sites were analyzed for the presence of bowhead whale song. We identified 12 unique song types sung by at least 32 individuals during ~95 h of recordings off Point Barrow. Six of these songs were detected at the Beaufort MARU site as well as six additional song types that were not analyzed. These results suggest a shared song repertoire among some individuals. This report represents the greatest number of songs to date during the spring migration for this population. We attribute this greater variety to population growth over the 30 yr since acoustic monitoring began in the early 1980s. Singing during early to mid‐spring is consistent with the hypothesis that song is a reproductive display, but further research is necessary to understand the exact function of this complex vocal behavior.     

Effects of sea ice extent and food availability on spatial and temporal distribution of polar bears during the fall open-water period in the Southern Beaufort Sea

We investigated the relationship between sea ice conditions, food availability, and the fall distribution of polar bears (Ursus maritimus) in terrestrial habitats of the Southern Beaufort Sea via weekly aerial surveys in 2000–2005. Aerial surveys were conducted weekly during September and October along the Southern Beaufort Sea coastline and barrier islands between Barrow and the Canadian border to determine polar bear density on land. The number of bears on land both within and among years increased when sea-ice was retreated furthest from the shore. However, spatial distribution also appeared to be related to the availability of subsistence-harvested bowhead whale (Balaena mysticetus) carcasses and the density of ringed seals (Phoca hispida) in offshore waters. Our results suggest that long-term reductions in sea-ice could result in an increasing proportion of the Southern Beaufort Sea polar bear population coming on land during the fall open-water period and an increase in the amount of time individual bears spend on land.     

Entanglement‐scar acquisition rates and scar frequency for Bering‐Chukchi‐Beaufort Seas bowhead whales using aerial photography

The Bering‐Chukchi‐Beaufort Seas (BCBS) bowhead whale (Balaena mysticetus) has been considered at low‐risk for entanglement injuries and ship strikes because their range is mainly north of commercial fisheries; nevertheless, changes to their arctic habitat, including a longer open water period and declining sea ice, have resulted in increasing commercial activity and concern about fisheries interactions. We examined interyear matches (between 1985 and 2011) from a photo identification project and identified whales that had acquired entanglement injuries. We estimated the probability of a bowhead acquiring an entanglement injury using two statistical methods: interval censored survival analysis and a simple binomial model. Both methods give similar results, suggesting a 2.2% (95% CI: 1.1%–3.3%) annual probability of acquiring a scar. We also include an entanglement scar frequency analysis of aerial photographs from the 2011 spring and fall surveys near Point Barrow, Alaska, which suggest 12.4% of live bowheads show evidence of entanglement scarring. Entanglement rates for the BCBS bowhead stock are lower than many other large whale stocks, and abundance has increased over the past 35 yr; however, our findings indicate that fishing gear entanglement is a more serious concern for the BCBS bowhead whale population than previously thought.     

Population Structure of Pacific Cod <Emphasis Type="Italic">Gadus macrocephalus</Emphasis> in the Southern Part of the Range Based on the Microsatellite Analyses

The population structure of Pacific cod Gadus macrocephalus in the southern part of the range and adjacent regions is studied on the basis of the results of microsatellite analyses. Collected data indicate heterogeneity of this species population within the studied area. According to the obtained F_ST values, Pacific cod from the waters of the Republic of Korea (Yellow Sea side) and northwestern part of the Sea of Okhotsk significantly differ from all other studied regions (Table 4). Significant differentiation was also revealed between samples from the waters of the Tatar Strait and all other regions except for South Kurils Pacific cod (both Sea of Okhotsk and Pacific Ocean sides). These two latter sample collections were similar to each other as well. A low level of differentiation was also shown for the Peter the Great Bay and the East Sea/Sea of Japan waters of the Republic of Korea.     

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.