The dynamics of the abundance, age, and sex structure of the Solovetsky reproductive gathering of the Beluga whale Delphinapterus leucas (Onega Bay, White Sea)

Based on the data from long-term research in 1999?C2009 we studied the population dynamics of Beluga whales in the Solovetsky reproductive gathering (RG) in the White Sea. This aggregation of Beluga whales is formed each year in the second half of May after the break-up of fast ice and persists to September inclusive. The aggregation numbers about 100 individuals from visual observations, with long-term variations of 20?C30 individuals. The percentage of whales of different age groups also varied in the gathering depending on year, but typically one half was formed by mature animals and the other half consisted of immature whales and yearlings. There are two pronounced peaks in numbers for the summer season in the Solovetsky Beluga RG. The number of Belugas increased with the appearance of males and females that were ready to breed and females that were ready to bear calves. The daily dynamics of Belugas in the gathering largely depended on the time of day and tidal regime. In the summer season, the state of the sea and human impacts were key factors in number fluctuations of the Belugas of the Solovetsky RG. The revealed negative correlation of the long-term population of Belugas in the gathering on air temperature is considered as a special instance of general laws of the migration activities of Beluga whales in the White Sea.     

Seasonal hematology and serum chemistry of wild beluga whales (Delphinapterus leucas) in Bristol Bay, Alaska, USA

We collected blood from 18 beluga whales (Delphinapterus leucas), live-captured in Bristol Bay, Alaska, USA, in May and September 2008, to establish baseline hematologic and serum chemistry values and to determine whether there were significant differences in hematologic values by sex, season, size/age, or time during the capture period. Whole blood was collected within an average of 19 min (range=11-30 min) after the net was set for capture, and for eight animals, blood collection was repeated in a later season after between 80-100 min; all blood was processed within 12 hr. Mean hematocrit, chloride, creatinine, total protein, albumin, and alkaline phosphatase were significantly lower in May than they were in September, whereas mean corpuscular hemoglobin concentration, monocytes, phosphorous, magnesium, blood urea nitrogen, alanine aminotransferase, aspartate aminotransferase, γ-glutamyltranspeptidase, and creatinine kinase were significantly higher. Mean total protein, white blood cell count, neutrophils, and lymphocytes were significantly higher early in the capture period than they were later. No significant differences in blood analyte values were noted between males and females. Using overall body length as a proxy for age, larger (older) belugas had lower white blood cell, lymphocyte, and eosinophil counts as well as lower sodium, potassium, and calcium levels but higher creatinine levels than smaller belugas. These data provide values for hematology and serum chemistry for comparisons with other wild belugas.     

Population genetic structure and evolutionary history of North Atlantic beluga whales (Delphinapterus leucas) from West Greenland, Svalbard and the White Sea

Population structure in many Arctic marine mammal species reflects a dynamic interplay between physical isolating mechanisms and the extent to which dispersal opportunities are met. We examined variation within mtDNA and eight microsatellite markers to investigate population structure and demographic history in beluga whales in the North Atlantic. Genetic heterogeneity was observed between Svalbard and West Greenland that reveals limited gene flow over ecological time scales. Differentiation was also recorded between Atlantic belugas and two previously studied populations in the North Pacific, the Beaufort Sea and Gulf of Alaska. However, Bayesian cluster analysis of the nDNA data identified two population clusters that did not correspond to the respective ocean basins, as predicted, but to: (1) Arctic (Svalbard–White Sea–Greenland–Beaufort Sea) and (2) Subarctic (Gulf of Alaska) regions. Similarly, the deepest phylogeographic signal was between the Arctic populations and the Gulf of Alaska. Fitting an isolation-with-migration model yielded genetic abundance estimates that match census estimates and revealed that Svalbard and the Beaufort Sea likely diverged 7,600–35,400 years ago but have experienced recurrent periods with gene flow since then, most likely via the Russian Arctic during subsequent warm periods. Considering current projections of continued sea ice losses in the Arctic, this study identified likely routes of future contact among extant beluga populations, and other mobile marine species, which have implications for genetic introgression, health, ecology and behavior.     

Population-specific home ranges and migration timing of Pacific Arctic beluga whales (Delphinapterus leucas)

Two populations of beluga whales (Delphinapterus leucas), the Eastern Beaufort Sea (BS) and Eastern Chukchi Sea (ECS), make extensive seasonal migrations into the Pacific Arctic. However, the extent to which these populations overlap in time and space is not known. We quantified distribution and migration patterns for BS and ECS belugas using daily locations from whales tracked with satellite-linked transmitters. Home ranges and core areas in summer (July and August) and in each month (July–November), daily displacement, dispersal from core areas, and autumn migration timing were estimated. Distinct summer and fall distribution patterns and staggered autumn migration timing were identified for BS and ECS whales. Summer home ranges for each population had less than 10 % overlap. Monthly home ranges were also relatively distinct between populations except in September (up to 88 % home range overlap). A distinct east–west shift in focal area use occurred in September that persisted into October, with the two populations essentially switching longitudinal positions. Highest daily displacements occurred during the migratory period in September for BS whales and October for ECS whales, further indicating westward fall migration was offset between populations. Sexual segregation of males and females within a population also varied monthly. Autumn migration timing as well as differences in spatial and temporal segregation between BS and ECS beluga populations may be a result of maternally driven philopatry and population-specific adaptations to dynamically available resources. Our results contribute to the management of these populations by identifying seasonal area use and differences in migration patterns.     

Matriarchal genetic population structure of North American beluga whales Delphinapterus leucas (Cetacea: Monodontidae)

The North American beluga whale Delphinapterus leucas population has been divided into a number of putative geographical stocks based upon migration routes and areas of summer concentration. Nucleotide sequences of the mitochondrial DNA (mtDNA) control region were used to assess whether these geographical stocks are genetically distinct. Beluga whale samples from 25 sites were collected primarily from aboriginal subsistence hunts across North America from 1984 to 1994. Thirty-nine mtDNA haplotypes were identified in 628 beluga samples. No differences were found in the distribution of haplotypes between male and female beluga whales at any sampling site. These haplotypes segregated into two distinct assemblages in both a haplotype network and a neighbour-joining tree. The haplotype assemblages had a geographically disjunct distribution that suggests postglacial recolonization of the North American Arctic from two different refugia.
An analysis of molecular variance based on haplotype relationships and frequency indicated genetic heterogeneity among beluga whale summering groups ( P ≤ 0.001). Sequence divergence estimates between sampling sites also indicated geographical differentiation, particularly between samples taken at east Hudson Bay or St Lawrence River and the western or central Arctic. The results of this study show a high degree of philopatry to specific summering areas by this highly mobile animal.     

Hematology and serum chemistry values in the beluga (Delphinapterus leucas)

Normal values and ranges for 31 clinical hematology and serum chemistry tests are reported for the beluga or white whale (Delphinapterus leucas). The values were collected over a 6-yr period from eight belugas maintained for display at Sea World (San Diego, California, USA) facilities and represent long-term evaluations for each animal in a controlled environment. They represent the first report for a number of serum chemistry values for the beluga. Normal values such as these provide an important data base from which to detect diagnostically important changes in health status for belugas in a zoological setting. They also establish a baseline from which to evaluate differences in normal values in free-ranging belugas and from which to diagnose disease problems in wild populations.     

Anatomy of the heart of the beluga whale (Delphinapterus leucas)

The heart of the beluga whale (Delphinapterus leucas) is described from the dissection of seven specimens. As in most whales the heart is characterized by a transverse broadness and a flatness of the ventricles from one surface to the other and by an apex formed by both ventricles. Heart size parameters are used for comparison with parameters of other marine and land mammals. The heart width index (heart height/heart circumference) averages 31.3 in comparison to 28.7 for the Weddell seal and 39.0 for the felids. The right ventricle is relatively long and narrow with a mean length index (TS/heart height) of 64.7 and a mean breadth index (TP/heart height) of 38.7. These heart parameters are discussed in functional terms.     

Nursing behaviors of beluga calves (Delphinapterus leucas) born in captivity

The nursing behaviors of two beluga whale calves were observed for the first 55 days postpartum. For both calves, the total time spent nursing in a given period peaked around 7–10 days postpartum and then declined over time. One calf, however, was found to have an unusual decline in nursing at day 35 postpartum. Ten days later, this calf was diagnosed as having a bacterial infection and given antibiotics. This suggests that early detection of health problems may be possible by observing calves' nursing behavior. For both calves, their general nursing patterns were similar, although one calf consistently nursed more than the other. Both calves nursed roughly every half hour, neither showed any signs of a circadian pattern, and carryover effects for both calves were found, indicating that there was a relationship in the overall nursing pattern from one interval to the next. That is, if nursing dropped off during one interval, it was typically made up in the next interval. Zoo Biol 16:247–262, 1997. © 1997 Wiley-Liss, Inc.     

A risk‐management approach to a mycotic disease potential in captive beluga whales (Delphinapterus leucas)

In response to the isolation of Aspergillus fumigatus and other potentially pathogenic fungi in expired air from four of five captive beluga whales (Delphinapterus leucas), a systematic assessment of the magnitude and nature of the risks associated with this finding was conducted. Ten genera of ubiquitous fungi, most of which were potential pathogens, were isolated from the whales over a 16‐month period. During this same period, the whales did not exhibit any behavioral, physical, hematological, or biochemical indications of disease. All the genera of fungi isolated from the whales were also found in air and water samples taken throughout the facility. Opportunities for contamination of samples of expired air were identified. A decision tree, which incorporated subjective probability estimates, was created. The final risk‐management plan involved: 1) alterations to the management of the pool to reduce environmental contamination and opportunities for exposure to fungi, 2) more rigorous quality control for sample collection, and 3) an increased frequency of blowhole cultures. The animals at the facility, including the newborn calf, remained healthy during the 3 years after the risk‐management program. Zoo Biol 18:5–16, 1999. © 1999 Wiley‐Liss, Inc.     

Parental behavior of the beluga whale (Delphinapterus leucas) in natural environment

The parental behavior of beluga whales observed in a summer reproductive gathering (near Solovetsky Island, Onega Bay, White Sea) is described, including the parturition process. A tight association between the female and its newborn infant has been traced by the case study of a stillborn calf. Individual behavioral patterns of a mother and calves observable only in natural habitats are detailed.     

Fatty acid composition of the blubber in white whales (Delphinapterus leucas)

Fatty acid (FA) composition of the blubber in free-ranging white whales (Delphinapterus leucas) from Svalbard's waters was determined and compared with the fatty acid composition of potential prey species in an attempt to assess diet. This methodology is based on the common assumption that unique arrays of FAs found within groups of organisms are transferred, largely unaltered, up marine food chains and thus may be useful for assessment of diet composition. Complete-column blubber biopsies were sampled from white whales (n=7) during the summers of 1996 and 1997. All captured animals were adult males. FAs were extracted from 2–4 replicates taken from an area about 10 cm in front of the mid-dorsal ridge. FA data from a total of 12 potential prey species from the Svalbard area were compared to the white-whale blubber samples. Twenty-two FAs were consistently found in relative amounts >0.5% of the total FA composition in white whales. These FAs accounted for 94–96% of the total FAs present. The blubber was composed almost entirely of triacylglycerols. The major saturated FAs were 14:0 and 16:0; 16:1(n-7), 18:1(n-9) and 20:1(n-9) were the major monounsaturated FAs and 20:5(n-3) and 22:6(n-3) were the major polyunsaturated FAs. Sixteen of the 22 FAs consistently found in the white-whale blubber were also found in considerable amounts (>0.5% of total FAs) in most of the potential species. Principal Component Analysis run on these 16 FAs suggests that polar cod (Boreogadus saida) had the most similar FA composition to the white-whale blubber, followed by capelin (Mallotus villosus), the copepod Calanus hyperboreus and the shrimp Pandalus borealis. Accepted: 27 November 1999     

Arterial and venous vasculature of the heart of the beluga whale (Delphinapterus leucas)

The arteries and veins of the heart of the beluga whale (Delphinapterus leucas) are described from the dissection of nine specimens. The arterial distribution is composed of the basic mammalian pattern of two major vessels, the left and right coronary arteries, which supply the cardiac tissue. The venous drainage is provided by three major systems which are the great, middle, and small cardiac veins. The vascular characteristics of the heart of the beluga whale are the marked sinuosity of both coronary arteries and their main branches, the numerous large interarterial anastomoses between major vessels, and the duplication of vessels in parallel branches. These characteristics are discussed in functional terms and correlated with the diving ability of the species.     

Nucleotide sequence of the p53 cDNA of beluga whale (Delphinapterus leucas)

The cDNA (DNA complementary to RNA) of the p53 gene of the beluga whale (Delphinapterus leucas) was sequenced by the method of 5'- and 3'-rapid amplification of cDNA ends (RACE) with the cDNA made for the RNA obtained from fresh peripheral blood leukocytes isolated from two animals. Primers for the RACE method were synthesized based on the sequence of the DNA of beluga whale corresponding to exon 5 of the human p53 gene, which was determined after amplification of the DNA isolated from the liver from a beluga whale by using a pair of primers for the human sequence. The sequenced cDNA had a 2150-nucleotide length and contained the whole region corresponding to human exons 1 through 11. The reading frame was 1164 bp (base pair) long and began in exon 2 and ended in exon 11, coding for a 387-amino acid protein. The nucleotide sequence of the reading frame showed high similarity over 85% with pig, sheep, cow, and human genes. The similarities with the former two animals at the amino acid level were also more than 85%. Lower similarity of the beluga whale p53 gene was also found with those of lower tetrapods, fish and invertebrates.     

Chemical characterization of the oligosaccharides in beluga (Delphinapterus leucas) and Minke whale (Balaenoptera acutorostrata) milk

Carbohydrates were extracted from the milk of a beluga, Delphinopterus leucas (family Odontoceti), and two Minke whales, Balaenoptera acutorostrata (Family Mysticeti), sampled late in their respective lactation periods. Free oligosaccharides were separated by gel filtration and then neutral oligosaccharides were purified by preparative thin layer chromatography and gel filtration, while acidic oligosaccharides were purified by ion-exchange chromatography, gel filtration and high performance liquid chromatography (HPLC). Their structures were determined by 1H-NMR. In one of the Minke whale milk samples, lactose was a dominant saccharide, with Fuc(alpha1-2)Gal(beta1-4)Glc(2'-fucosyllactose), Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc(lacto-N-neotetraose), GalNAc(alpha1-3)[Fuc(alpha1-2)]Gal(beta1-4)Glc(A-tetrasaccharide), Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc (para lacto-N-neohexaose), Neu5Ac(alpha2-3)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc (sialyl lacto-N-neotetraose), Neu5Ac(alpha2-6)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc (LST c) and Neu5Ac(alpha2-3)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc (sialyl para lacto-N-neohexaose) also being found in the milk. The second Minke whale sample contained similar amounts of lactose, 2'-fucosyllactose and A-tetrasaccharide, but no free sialyl oligosaccharides. Sialyl lacto-N-neotetraose and sialyl para lacto-N-neohexaose are novel oligosaccharides which have not been previously reported from any mammalian milk or colostrum. These and other oligosaccharides of Minke whale milk may have biological significance as anti-infection factors, protecting the suckling young against bacteria and viruses. The lactose of Minke whale milk could be a source of energy for them. The beluga whale milk contained trace amounts of Neu5Ac(alpha2-3)Gal(beta1-4)Glc(3'-N-acetylneuraminyllactose), but the question of whether it contained free lactose could not be clarified. Therefore, lactose may not be a source of energy for suckling beluga whales.