Ecological characteristics of the ringed seal of the Kara Sea

Fisheries ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. 8-15
Author(s):  
Nikolay Gaydenok ◽  
Evgenniy Martynjuk ◽  
Gennadiy Ognetov

The quantitative distribution and features of the migration of ringed seals in the Kara Sea are analyzed. An estimate of the abundance, demographic and trophoenergetic indicators is obtained.

1998 ◽  
Vol 1 ◽  
pp. 63 ◽  
Author(s):  
Stanislav E Belikov ◽  
Andrei N Boltunov

This paper presents a review of available published and unpublished material on the ringed seal (Phoca hispida) in the western part of the Russian Arctic, including the White, Barents and Kara seas. The purpose of the review is to discuss the status of ringed seal stocks in relation to their primary habitat, the history of sealing, and a recent harvest of the species in the region. The known primary breeding habitats for this species are in the White Sea, the south-western part of the Barents Sea, and in the coastal waters of the Kara Sea, which are seasonally covered by shore-fast ice. The main sealing sites are situated in the same areas. Female ringed seals become mature by the age of 6, and males by the age of 7. In March-April a female gives birth to one pup in a breeding lair constructed in the shore-fast ice. The most important prey species for ringed seals in the western sector of the Russian Arctic are pelagic fish and crustaceans. The maximum annual sealing level for the region was registered in the first 70 years of the 20th century: the White Sea maximum (8,912 animals) was registered in 1912; the Barents Sea maximum (13,517 animals) was registered in 1962; the Kara Sea maximum (13,200 animals) was registered in 1933. Since the 1970s, the number of seals harvested has decreased considerably. There are no data available for the number of seals harvested annually by local residents for their subsistence.


1987 ◽  
Vol 65 (4) ◽  
pp. 1021-1027 ◽  
Author(s):  
Christian Lydersen ◽  
Ian Gjertz

Samples were taken from 284 ringed seals (Phoca hispida) in the Svalbard area during April–July 1981 and March–April 1982. The age of 283 seals was determined by reading annuli in the cementum of the canine teeth. The mean age of the males was 11.3 years, and of the females, 14.9 years. Females were found to be significantly older than males. The mean length of sexually mature ringed seals was 128.9 cm for both sexes. The mean weight of adult males and females was 53.5 and 61.4 kg, respectively. Females were found to be significantly heavier than males. The sex ratio was 47.8% males and 52.2% females. Studies of microscopic sections of testis and epididymis from ringed seal males showed that 63, 75, and 80% of 5-, 6-, and 7-year-old animals, respectively, were sexually mature. The weights of testis and epididymis, diameters of tubuli, and the size of testis all showed a marked increase in the 5-year age-class. Macroscopic sections of ovaries from ringed seal females showed that 20, 60, and 80% of 3-, 4-, and 5-year-old animals, respectively, were sexually mature. The size of the ovaries showed a marked increase in the 5-year age-class. The ovulation rate of ringed seals from Svalbard was calculated to be 0.91.


2021 ◽  
Vol 40 ◽  
Author(s):  
Magnus Andersen ◽  
Kit M. Kovacs ◽  
Christian Lydersen

Ringed seals, which are small phocid seals, range across the circumpolar Arctic, and have evolved in close association with sea ice and depend on it for all aspects of their life history. This research study compares age structure, reproductive parameters, body size and condition during three time periods—1981–82 (n = 277), 2002–04 (n = 272) and 2012–18 (n = 212)—to study potential changes in demography in ringed seals in western Svalbard, Norway, an area that has undergone dramatic changes in sea-ice conditions during recent decades. Age distributions for the three time periods were similar, with the exception that the most recent period had a higher proportion of young animals. Age at sexual maturity for both sexes was similar for the two most recent periods, both being lower than in the 1980s. Ovulation rates did not vary significantly among the three periods (range 0.86–0.94). Pregnancy rates were only available for the most recent study period (0.71); this value falls within the range reported from other Arctic regions. Body length showed no clear temporal patterns; males were slightly longer in the most recent period, while females were slightly longer in the first period. Data from May in all periods suggest that body condition has not varied significantly through time. In conclusion, although the ringed seal breeding habitat in Svalbard has declined significantly in recent decades, demographic parameters appear to be largely unaffected. Life-history plasticity in combination with a small-scale regional variation in environmental conditions might explain the lack of changes in demography over time.


Oceanology ◽  
2017 ◽  
Vol 57 (1) ◽  
pp. 154-164
Author(s):  
A. A. Udalov ◽  
D. V. Kondar ◽  
M. A. Miljutina ◽  
D. M. Miljutin ◽  
F. V. Sapojnikov ◽  
...  

2021 ◽  
Author(s):  
Rowenna Gryba ◽  
Henry P Huntington ◽  
Andrew L. Von Duyke ◽  
Billy Adams ◽  
Brower Frantz ◽  
...  

Indigenous people possess information of animals’ habitat use and behaviour; information essential for management and conservation of species affected by climate change. Accessibility of species that are important to Indigenous hunters may also change with environmental conditions. We documented Indigenous Knowledge of bearded (ugruk in Iñupiaq), ringed (natchiq), and spotted seals (qasigiaq) in Utqiaġvik, Alaska, using semi-directed interviews with Iñupiaq hunters. This study originated from discussions with an agency of the regional municipal government to serve co-management efforts and understand habitat use of species subjected to climate change. Results indicated that ringed seals are associated with higher ice concentrations in winter than bearded seals and changes in sea ice retreat in spring may have greater impact on ringed seal habitat use because they are more likely to haul out on ice in spring. Additionally, all three species have foraging hotspots, used over several days by multiple individuals. Bearded seals, and to a lesser extent spotted and ringed seals, will use currents to forage. Results also revealed the use of inland water bodies and terrestrial habitat, which may become more important for bearded and ringed seals with changing ice concentrations and should be considered in management and conservation of these species.


1998 ◽  
Vol 1 ◽  
pp. 46 ◽  
Author(s):  
Christian Lydersen

The ringed seal is the most abundant mammal in the Svalbard area. Annual pup production in this area is estimated to be 20,000. No systematic harvest records exist, but some few hundred seals are taken annually, mainly for dog food. The ringed seals in Svalbard are protected from hunting in the period 15 March - 15 April. Peak pupping season is the first week of April. New-born ringed seals weigh an average of 4.6 kg. They are nursed for about 39 days, and weaned at an average body mass of around 22 kg. During the period of maternal care pups consume a total of about 54 litres of milk, that is composed of approximately 38% fat and 10% protein. Asymptotic standard lengths and body masses for adult ringed seal males and females are 131.5 and 127.8 cm, and 52.6 and 59.9 kg,respectively. The maximum values recorded for lengths of males and females in Svalbard are 157 cm and 107 kg, respectively. There is marked seasonal variation in body mass in both sexes with the highest mass records being recorded in early spring before pupping occurs, and with minimum values in the summer after the breeding and moulting seasons. The observed variation in mass is mainly due to changing blubber thickness of the seals. Ringed seal males attain sexual maturity at the age of 5 - 7 years, while females reach maturity when they are 3-5 years of age. The oldest seal collected in Svalbard was aged 45. Ringed seals in the Svalbard area feed on a variety of prey organisms, the most important of which are polar cod (Boreogadus saida) and the crustaceans Parathemisto libellula, Thysanoessa inermis and Pandalus borealis. Ringed seal pups start diving during the nursing period while they are still white-coats, and spend about 50% of the time in thewater prior to weaning. They are capable of diving for up to 12min and dive to the bottom of the study areas (max. 89 m). Nursing females spend more than 80% of their time in the water. Maximum recorded dive duration for mothers was 21.2 min. In order to produce a weaned pup, the net energy expenditure for a ringed seal mother is 1,073 MJ. This energy value corresponds to the consumption of 185 kg of polar cod or 282 kg of P. libellula. The annual gross energy consumption for adult males and females is calculated to be 5,600 MJ and 7,300 MJ, respectively. The main predators of ringed seals in Svalbard are polar bears (Ursus maritimus) and Arctic foxes (Alopex lagopus). In addition, both glaucous gulls (Larus hyperboreus) and walruses (Odobenus rosmarus) are documented as predators of ringed seals in this area. Heavy predation pressure is probably the main factor explaining why pups of this species start diving at such a young age, why they have access to so many breathing holes (8.7 on average) and why they keep their white coat long after its thermoregulatory properties have vanished. Pollution levels in ringed seals from Svalbard are, generally speaking, similar to levels in other areas of the Arctic.


1996 ◽  
Vol 74 (5) ◽  
pp. 858-874 ◽  
Author(s):  
C. M. Furgal ◽  
K. M. Kovacs ◽  
S. Innes

Characteristics of ringed seal (Phoca hispida) subnivean structures and breeding habitat were quantified and their potential influence on predation success by polar bears (Ursus maritimus), arctic foxes (Alopex lagopus), and humans on ringed seals was investigated in Admiralty Inlet and Strathcona Sound, Northwest Territories. A total of 237 ringed seal structures were located between April and June 1991–1993 using trained dogs. Ringed seal lairs and breathing holes were concentrated in areas of deep snow, and were associated with large, thick ice ridges. Only a small percentage of the available fast-ice habitat had sufficient snow depth for lair construction each year. A discriminant function analysis used to classify structures located in 1992, using a combination of structural and habitat measurements, correctly classified 70% of structures located in 1991 and 1993 into functional groups. The length, width, internal height, and level of "tiggak," the odour of rutting male ringed seals, associated with structures were the most important descriptors separating structure types. Seventy-three percent of structures located in the study were undisturbed by predators. The mean length and width of structures entered by predators were significantly greater than those of undisturbed structures. Polar bear success decreased as snow depth and the thickness of the roof covering the structures increased. The conditions necessary for successful arctic fox predation are unclear. Inuit hunters attacked structures close to ice ridges, and ridge height and snow depth influenced their success. All predators attacked lairs having the odour of rutting male ringed seals less often than structures with no male odour.


1991 ◽  
Vol 48 (12) ◽  
pp. 2471-2476 ◽  
Author(s):  
M. O. Hammill ◽  
C. Lydersen ◽  
M. Ryg ◽  
T. G. Smith

Length of lactation, pup growth rate, and female weight loss in ringed seals (Phoca hispida) were estimated using cross-sectional data from the Canadian and Norwegian Arctic. At birth the pups had a standard length of 63.4 cm (SE = 1.3, N = 11) and weighed 5.4 kg (SE = 0.4, N = 6). Weaning occurred approximately 39 d (range 36–41 d) after birth at an estimated length of 88.4 cm (SE = 0.65, N = 96) and an estimated weight of 22.1 kg, resulting in an increase in length of 0.64 cm∙d−1 and a weight change of 0.43 kg∙d−1. Regression of female weight on the number of days after the nominal date of birth for each region indicated that the postpartum female weighed 81.2 kg and lost 0.64 kg∙d−1 (95% CI = ±0.20). During lactation, female weight declined by an estimated 32%, with much of the loss occurring from the blubber. Analyses of stomachs indicated that ringed seals supplemented stored energy reserves by feeding during lactation.


2001 ◽  
Vol 79 (8) ◽  
pp. 1455-1464 ◽  
Author(s):  
Michael A Simpkins ◽  
Brendan P Kelly ◽  
Douglas Wartzok

We analyzed the three-dimensional movements within individual dives of five freely swimming ringed seals (Phoca hispida). We divided dives into a series of moves, each of which represented continuous movement in one direction, and evaluated several three-dimensional movement variables to distinguish between types of movement within dives. Horizontal directionality proved to be the most useful variable, and we distinguished convoluted and directional movements by fitting a mixture of two normal distributions to the observed horizontal-directionality values. Both convoluted and directional movements occurred within each phase of most dives, suggesting that ringed seals switched between behavioral modes within dive phases. Descent and ascent phases were not simply travel behavior, nor were bottom phases equivalent to patch time, complicating the formulation of optimal diving models for ringed seals. Most ringed seal dives appeared to consist of a series of patch times separated by travel times. Travel behavior accounted for the majority of dive times.


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