Seasonal changes in body mass and body composition of ringed seals (Phoca hispida) on Svalbard

1990 ◽  
Vol 68 (3) ◽  
pp. 470-475 ◽  
Author(s):  
Morten Ryg ◽  
Thomas G. Smith ◽  
Nils Are Øritsland

Seasonal changes in body mass and body composition of ringed seals (Phoca hispida) from the Svalbard Islands are described. The blubber content of adult females decreased from a high of about 50% at the beginning of the pupping season in March–April to a low of 31% during moulting in June. In adult males, the blubber content decreased from 41% in March to 29% in June. By estimating an individual seal's body mass by 1 April from its standard body length, we calculated an average daily loss of body mass of 160 g/day in adult females and 100 g/day in adult males from the start of lactation to the middle of moulting. The blubber content of sexually immature seals was less in June and July than in April, but the seasonal changes were smaller than in adult seals. We found no evidence of significant changes in core mass in adult seals, and suggest that the seasonal body mass changes are mostly due to changes in body fat content.

1996 ◽  
Vol 74 (1) ◽  
pp. 136-146 ◽  
Author(s):  
K. L. Gerhart ◽  
R. G. White ◽  
R. D. Cameron ◽  
D. E. Russell

We determined seasonal changes in body mass and composition of arctic caribou (Rangifer tarandus granti) in relation to age and reproductive status. Chemical composition was determined for 37 caribou calves from the Central Arctic Herd ranging from 1 to 134 days of age and for 15 adult females collected from the same herd in October, May, and July. Body composition of 5 fetuses from the Central Arctic Herd, 13 calves from the Porcupine Herd, and 10 captive male reindeer (R. t. tarandus) was determined for comparison. Between October 1989 and May 1990, body fat and protein of adult females declined by maxima of 45 and 29%, respectively; an additional 32% of fat was lost between May and July. Mobilization of large amounts of fat and protein suggests winter undernutrition. Chemical composition and growth patterns of calves did not differ between the herds. The growth rate of Central Arctic Herd calves was high during the first 28 d post partum (402 g/d), but both growth rate and fatness declined between 4 and 6 weeks of age (to 306 and −18.3 g/d, respectively), perhaps in response to insect harassment. Birth masses of males and females did not differ, but by autumn, male calves were 9.1 kg heavier than females. Chemical components (water, fat, protein, ash) were highly correlated with body mass, ingesta-free body mass, and carcass mass. Percentages of fat and water were inversely related, but the intercept decreased with age. Marked seasonal hypertrophy of liver and kidneys was noted in caribou, suggesting the presence of mobilizable protein reserves. Seasonal changes in organ masses may also reflect variations in metabolic activity and nutrient intake.


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.


Mammalia ◽  
2004 ◽  
Vol 68 (4) ◽  
Author(s):  
Jorge A. Encarnação ◽  
Markus Dietz ◽  
Uwe Kierdorf ◽  
Volkmar Wolters

Body mass changes of adult and juvenile male Daubenton’s bats were studied in a summer habitat in Hesse (Germany) in the years 1998-2001. Animals from the resident population were regularly captured along the flight path from April to October, and body mass was determined using a digital balance. Body mass of adult individuals differed significantly among fortnightly periods (Kruskal-Wallis ANOVA by ranks: H = 141.75, p < 0.001). Body mass increased significantly from the second half of April (median: 7.0 g) to the first half of May (median: 7.8 g). Between the second half of May and the first half of August, median body mass fluctuated between 7.8 g and 8.3 g. From the second half of July (median: 7.9 g) to the second half of August (median: 8.4 g), and the second half of September (median: 9.3 g) body mass again significantly increased. The highest median body mass (9.6 g) was recorded in the second half of October. Median body mass of juvenile males ranged between 6.5 g in the first half of July and 8.5 g in the second half of October. Differences in body mass over the studied period were significant (H = 21.70, p < 0.01). During the months July, August, and September, body mass of adult males was significantly higher than that of juveniles, whereas in October the difference was no longer of statistical significance. It is suggested that the decrease in body mass observed in some adult males in September was related to their reproductive activity.


1991 ◽  
Vol 70 (3) ◽  
pp. 994-997 ◽  
Author(s):  
G. B. Forbes

We assessed changes in body composition in 41 young adults who engaged in various exercise and/or training programs on ad libitum diets. Most of those who gained weight sustained an increase in lean body mass (LBM), and most of those who lost weight lost LBM as well as fat. The change in LBM was directly related to the change in weight, with a regression slope of 0.500. An analysis of published data confirms these findings and, in concert with our data, provides the additional information that the magnitude of the change in body composition in exercising individuals is influenced by body fat content, just as it is for nonexercising individuals.


2008 ◽  
pp. 735-744
Author(s):  
AV Sirotkin ◽  
P Chrenek ◽  
J Rafay ◽  
R Omelka ◽  
H Vetr ◽  
...  

The aim of these studies was to compare some endocrine and non-endocrine characteristics of transgenic (carrying mammary gland-specific mWAP-hFVIII gene construct) and non-transgenic rabbits. The concentrations of corticosterone, progesterone, testosterone, estradiol, insulin-like growth factor I (IGF-I) and human factor VIII (hFVIII) in the blood plasma of adult females (9 months of age, 3rd generation transgenic animals), adult males, and young females (1-2 months of age, 4th generation of transgenic animals), as well as in the milk of lactating adult females, were analyzed by using RIA. In addition, litter size and body mass of pups born by transgenic and non-transgenic females from the 3rd generation were compared. Transgenic animals were compared with their non-transgenic siblings (the same genetic and epigenetic background). Transgenesis did not influence plasma hFVIII, but significantly increased corticosterone (in all animals), reduced IGF-I (in adult males and females), testosterone and estradiol, (in young females) and altered progesterone (increase in adult males and decrease in adult females) concentrations in blood plasma. In addition, transgenic females had higher milk concentrations of testosterone, but not progesterone or IGF-I than their nontransgenic sisters. These endocrine changes were not associated with changes in litter size. Transgenic male (but not female) pups have smaller body mass than control animals. These observations demonstrate the influence of transgenesis per se on the animal growth and endocrine system (secretion of reproductive and stress steroid hormones as well as growth factors) over four generations.


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.


1993 ◽  
Vol 71 (5) ◽  
pp. 1041-1045 ◽  
Author(s):  
Lyn C. Branch

Activity patterns of adult male, adult female, and immature plains vizcacha (Lagostomus maximus) were compared throughout the year, and seasonal changes in body mass were documented for adults. All sex–age classes spent more time feeding in winter and less time at the den site (vizcachera) than in other seasons. The pattern was reversed for summer. Seasonal changes in activity budgets for males were associated with an increase in male–male conflicts and territorial displays at the vizcachera. Body mass of males declined in summer, when they were competing for access to areas used by females, and reached a minimum during the fall breeding season. Females spent less time foraging and more time at the den site after parturition in spring. Body mass of females did not change significantly with season. Throughout the year, activity patterns were similar for females and immatures. During all seasons, adult males spent less time foraging and more time at the vizcachera than other sex–age classes did. From a variety of observations, I suggest that the costs of reproduction, including mass loss, shorter feeding time, and short tenure in a social group, are high for male vizcachas.


Parasitology ◽  
2015 ◽  
Vol 142 (10) ◽  
pp. 1260-1269 ◽  
Author(s):  
QUINN M. R. WEBBER ◽  
ZENON J. CZENZE ◽  
CRAIG K. R. WILLIS

SUMMARYParasite dynamics can be mediated by host behaviours such as sociality, and seasonal changes in aggregation may influence risk of parasite exposure. We used little brown bats (Myotis lucifugus) captured during the autumn mating/swarming period to test the hypothesis that seasonal and demographic-based variation in sociality affect ectoparasitism. We predicted that ectoparasitism would: (1) be higher for adult females and young of the year (YOY) than adult males because of female coloniality; (2) increase for adult males throughout swarming because of increasing contact with females; (3) decrease for adult females and YOY throughout swarming because of reduced coloniality and transmission of individual ectoparasites to males; (4) be similar for male and female YOY because vertical transmission from adult females should be similar. Ectoparasitism was lowest for adult males and increased for males during swarming, but some effects of demographic were unexpected. Contrary to our prediction, ectoparasitism increased for adult females throughout swarming and YOY males also hosted fewer ectoparasites compared with adult and YOY females. Interestingly, females in the best body condition had the highest parasite loads. Our results suggest that host energetic constraints associated with future reproduction affect pre-hibernation parasite dynamics in bats.


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