Search

The spatiotemporal distribution of harp seal pups around breeding grounds in the White Sea is considered. It is shown that spatial localization of groups of females with different terms of mass pup birth takes place. This somewhat confirms the data on the gregarious structure of White Sea harp seal population. It is possible to explain the structure of this adaptation of the seal population to different living conditions in different feeding areas.

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.

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.

The structure of the summer reproductive gathering of beluga whales Delphinapterus leucas was studied in the vicinity of Myagostrov, Golyi Sosnovets, and Roganka islands (Onega Bay, the White Sea) in 2006 and 2008. The abundance, age and sex structure, behavior, and swimming and acoustic behavior were studied in detail.

Based on the data from long-term research in 1999–2009 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 20–30 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.

The underwater vocalizations of the beluga whale summering in Onega Bay (64°24′N, 35°49′E) were recorded in June–July of 2008. The vocalizations were classified into five major whistle types, four types of pulsed tones, click series, and noise vocalizations. To determine the relationship between the behavioral activity and the underwater vocalizations, a total of fifty-one 2 minute-long samples of the audio records were analyzed in the next six behavioral contexts: directional movements, quiet swimming, resting, social interactions, individual hunting behavior, and the exploration of hydrophones by beluga whales. The overall vocalization rate and the percentage of the main types of signals depend on the behavior of the belugas. We suggest that one of the whistle types (the “stereotype whistle”) is used by belugas for long-distance communications, while other whistle types (with the exception of “squeaks”) and three types of pulsed tones (with the exception of “vowels”) are used for short distance communication. The percentage of “squeaks” and “vowels” was equally high in all the behavioral situations. Thus, we assume that “squeaks” are contact signals. “Vowels” have a specific physical structure and probably play a role in identification signals. A high rate of the click series was observed in the process of social interactions.

The structure of the reproductive gathering of beluga whales (RG) was studied near Cape Beluzhii in the Solovetsky Islands in the White Sea by the photo identification of individuals in 2007–2008; in addition, the peculiarities of the seasonal and interseasonal dynamics of the RG incomings were analyzed. The gathering is formed by predominantly females and calves of different ages, which visit the RG area as stable “family” groups. About 15% of the observed females come to Beluzhii Cape every year and stay there during the whole summer season; thus, forming the regular part of the RG. The other animals come there for a certain time period, which is probably preconditioned by their physiological readiness for coupling and procreation for some of the females. When comparing our data with the catalogue of the visually registered beluga whales’ markers (1996–2008), we found that most of the identified animals of the Solovetsky RG appear here during one summer season or even with an off period of several years despite the significantly regular findings of most of them for this area. We conclude this may be linked with the natural changes of the individual markers due both to the shedding and the sexual cycle in the mature animals. Our data allow concluding that the total population of the Solovetsky PG is higher than was reported before using the visual supervision methods.

Data on the white whale distribution in Onega Bay of the White Sea obtained during route and stationary observations in the summer of 2003–2006 are given. The presence of three regions of summer habitation of local “nonmigratory” white whale reproductive schools is confirmed. The minimum abundance of the “zhizhginskoe” (northeastern) school is 60 individuals, and the minimum abundance of the “myagostrovskoe” (western) is 50 individuals. The abundance of the best studied “southern” school is close to 120–130 individuals. One more region of white whale concentration (with an abundance of up to 40 individuals) (the eastern one; Cape Letniy Orlov-Cape Chesmenskiy) was found. The localization of single reproductive schools (RS) is due to a number of factors: the morphometry of the shores and bottom, the hydrological regime, and the character of the coastal tidal currents. The white whale distribution in the southern part of Onega Bay in the summer (June–July) is of discontinuous character with concentrations near cape Glubokiy and some other adjacent parts. The coefficient of the white whale attendance in the Cape Glubokiy area varied from 42.5 to 67.4% during the years of the studies (2003–2006). The character of the distribution, the direction of the relocations, and the animals’ behavior peculiarities indicate that the white whales of the southern part of Onega Bay of the White Sea form a rather stable school community of a few (5–6) locally distributed small family groups during the summer.

The periods of development individual behavior in beluga calves are described. During these periods, calves form locomotor skills and interrelations with other individuals, and this determines the overall social structure of a pod. The formation of behavior in White Sea beluga calves passes through a number of stages. New types of social interactions arose in the following sequence: the imprinting period, the first abandoning of the mother without contact with other members of the pod and accumulation of new locomotive elements, first contacts with other young-of-the-year calves, and the complication of interaction types through game activities. Calves usually formed pairs with coevals or elder calves that possessed a richer locomotor repertoire. New motions appeared as a result of imitation of adult animals. These periods do not have distinct terms and depend on the individual qualities of the calves. Some changes in the belugas’ behavior were seen under the conditions of the active development of managed ecotourism in the area around Solovetsky Island, the animals showed adaptation to the presence of man.

Whistles recorded in a reproductive gathering of beluga whales near Solovetskii Island in the White Sea are analyzed. On the basis of the absolute characteristics and shape of the frequency contour, whistles are classed into 16 types. Whistles belong to a relatively low frequency band, contain many harmonics, and have a simple shape of frequency contour. The average whistle duration varies from 0.1 to 1.7 s for different types, the average value of the maximum fundamental frequency varies from 1.4 to 4.5 kHz, and the average number of inflection points is from 0 to 9 per signal. In contrast to other populations, where flat whistles are the most frequent vocalizations, beluga whales observed in the reproductive gathering in the White Sea most often produce short whistles with a V-shaped frequency contour.

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.

High-frequency whistles of beluga whales are analyzed. The signals are recorded in a belgua summer assemblage off Solovetskii Island in the White Sea. The high-frequency whistles are narrowband signals with a continuous waveform and a fundamental frequency above 5 kHz. On the average, they make up 7.7% of the total vocal production of the animals. Based on the shape of the fundamental frequency contour and its time-frequency parameters, the high-frequency whistles are classed into 12 types. The HF whistles have a mean fundamental frequency of 9.7 kHz, an average bandwidth of 3.3 kHz, and an average duration of 1.0 s. The number of inflection points per signal ranges from 0 to 56 with a mean of 2.3. The predominant types are flat (50%), rising (23%), and wavy (7%) high-frequency whistles. Presumably, beluga whales can use some of the whistle types for short-range communication and other types for long-range communication.

Elements of behavior under natural conditions, their duration, and frequency are described in three age groups of belugas calves: newborn, one-month-old, and two-month-old. The quantitative and qualitative indices of the recognized behavioral elements allowed us to evaluate the mother-infant contacts and to analyze their dynamics during calf growth. The most common calf positions relative to the mother during this period were "at the cow's tail" and "at the cow's side." The importance of behavioral responses of calf for the development of social behavior in adult animals is emphasized.

The set of acoustic signals of White-Sea white whales comprises about 70 types of signals. Six of them occur most often and constitute 75% of the total number of signals produced by these animals. According to behavioral reactions, white whales distinguish each other by acoustic signals, which is also typical of other animal species and humans. To investigate this phenomenon, signals perceived as vowel-like sounds of speech, including sounds perceived as a “bleat,” were chosen A sample of 480 signals recorded in June and July, 2000, in the White Sea within a reproductive assemblage of white whales near the Large Solovetskii Island was studied. Signals were recorded on a digital data carrier (a SONY minidisk) in the frequency range of 0.06–20 kHz. The purpose of the study was to reveal the perceptive and acoustic features specific to individual animals. The study was carried out using the methods of structural analysis of vocal speech that are employed in lingual criminalistics to identify a speaking person. It was demonstrated that this approach allows one to group the signals by coincident perceptive and acoustic parameters with assigning individual attributes to single parameters. This provided an opportunity to separate conditionally about 40 different sources of acoustic signals according to the totality of coincidences, which corresponded to the number of white whales observed visually. Thus, the application of this method proves to be very promising for the acoustic identification of white whales and other marine mammals, this possibility being very important for biology.

The structure of the summer reproductive gathering of beluga whales Delphinapterus leucas was studied in the vicinity of Myagostrov, Golyi Sosnovets, and Roganka islands (Onega Bay, the White Sea) in 2006 and 2008. The abundance, age and sex structure, behavior, and swimming and acoustic behavior were studied in detail.

Results of the perceptive and acoustic analysis of communicative pulsed signals recorded in a repro- ductive gathering of beluga whales off Solovetskii Island in the white sea are presented. The mean signal dura- tion varies from 0.04 to 1.52 s for various signal types, the pulse repetition rate on the average ranges from 13 to 1300 (possibly, 2700) impulses per second, and the mean peak frequency falls within 0.2 to 11.3 kHz. A high degree of similarity between the communicative pulsed signals produced by beluga whales from different pop- ulations is revealed.

It is quite natural that individuals of many mammalian species, including humans and dolphins, often have individual vocal reactions. Due to this specificity, animals are aware of the location, the level of arousal or something else about their neighbors. For example, during stress situations dolphins produce stereotyped signalizations (McBride and Kritzler, 1951; Dreher and Evans, 1964; Evans, 1967; Busnel and Dziedzic, 1968). As it was shown in oceanaria, this type of signalization is their own individual signals (Caldwell and Caldwell, 1965, 1968, 1971; Caldwell et al., 1971, 1973 a,b; Sidorova et al., 1990).

The detection of odontocete echolocation signals with acoustic loggers has proved to be a very effective way to monitor their distribution, seasonal patterns and habitat use. However, belugas (Delphinapterus leucas) have never been monitored using this methodology. In order to evaluate its viability, echolocation signals of captive belugas were analyzed and the performance of T‐POD (Chelonia Ltd., UK) acoustic loggers in captivity and in the Arctic environment was tested. Results from captivity demonstrated the potential of beluga remote monitoring by T‐PODs. Field tests were organized in different environmental conditions with different populations of belugas to ensure the validity and detection robustness of this method. T‐PODs were deployed in Svalbard (Norway) in Spring 2007, in Yakutat (Alaska) in Spring 2008, and in Solovetsky (Russia) in Summer 2008. Instruments were deployed concurrently with visual observations and hydrophone recordings to compare presence/absence data from the three different methods. Results proved that T‐PODs positively detected all the identified periods of beluga presence without false detections and revealed temporal distribution correlations with tide levels, feeding behaviors, and circadian rhythms in the echolocation activity. Results from this project indicate that beluga remote monitoring is feasible in the Arctic environment using acoustic loggers.

An active acoustic technique for monitoring the whales is proposed. The technique allows one to monitor the whales’ crossing of a conventional borderline extending for several tens of kilometers in a shallow-water area. The potentialities of the technique are demonstrated in the framework of a numerical experiment by solving the problem of diffraction by model scatterers in an acoustic waveguide. The scatterers are selected in the form of soft spheroids with dimensions characteristic of various kinds of cetaceans.