Are non-migrant white storks (Ciconia ciconia) able to survive a cold-induced fast?

Northwestern European populations of White Storks (Ciconia ciconia) have been restored by settling young birds which, after having been maintained captive for 3 years, do not migrate when released. Since they are still supplied with food, the question we address here is how settled White Storks would cope with a fast resulting from a cold spell if food were no longer available. We therefore measured daily body mass loss, nitrogen excretion and daily energy expenditure under natural photoperiod and climatic conditions in six captive White Storks exposed to 5 days of food deprivation during winter. Daily ambient temperature ranged between -10 and 17 degrees C. After an initial decrease in both daily body mass loss and nitrogen excretion during the first day of fasting, these two parameters stabilized at low values. Lipids were the main fuel energy source (91%) and body proteins accounted for the remainder (9%). The rate of CO(2) production, measured with the doubly labeled water method, decreased significantly (P<0.001) during fasting when compared to the ad libitum value. Our data show that the metabolic adjustments of White Storks facing starvation are similar to those found in birds well-adapted to long-term fasting. From the determination of lipid and protein stores and of lipid and protein depletion rates, we conclude that White Storks would be able to survive at least during 4 weeks, a period of time twice as long as the duration of cold spells usually occurring in the Alsace region.     

Energetics of the annual cycle of Dippers Cinclus cinclus

Time-activity budgets and energy expenditure of Dippers Cinclus cinclus were studied in all months of the year and for every stage of the annual cycle. The commonest daytime activity was feeding (54%), then resting (43%) and flying (4%). On a 24-hr day basis the most marked changes in activity followed from changing daylengths. DEE (Daily Energy Expenditure), derived from time-activity budgets through the year and laboratory estimates of metabolism, averaged 201 kj d ^-1 in females and 228 kj d ^-1 in the larger males. Over a more restricted range of circumstances, direct estimates of DEE obtained from 77 Dippers using the doubly labelled water technique averaged 205 ± 43 kj d^-1 and 251 ± 55 kj d^-1 in females and males, respectively. Overall, the correspondence between these largely independent estimates of energy expenditure was reasonably close. DEE was highest during breeding (laying-females; rearing-males) and in late winter for both sexes. The lowest energy expenditures occurred during moult, amongst juveniles and in early winter. Incubating females and mate-guarding males also had low energy costs. Across all stages of the annual cycle body size, activity patterns, ambient temperature and river flow had significant effects on energy expenditure. The rate at which food was gathered to meet these changing energy demands varied widely. While some of this variation was imposed by a seasonal environment, it was also likely to reflect adaptive shifts in rates of food gathering, in some cases consequent upon the changing fitness benefits of various non-feeding activities.     

Sex- and concentration-dependent effects of predator feces on seasonal regulation of body mass in the bank vole Clethrionomys glareolus

Increased perception of predation risk can cause changes in activity, feeding and reproductive behavior in a wide range of taxa. Many small mammals in the temperate zone exhibit fluctuations in body mass in response to changing photoperiod. Bank voles lose body mass in winter which they regain when photoperiod increases in the spring. To determine if predation risk affects seasonal changes in body mass (BM), bank voles were exposed to two concentrations (low: LC and high: HC) of weasel feces. Food intake (FI) and daily energy expenditure (DEE) were measured to establish if differences in body mass were due to adjustment in energy intake or expenditure. Fecal corticosterone (CORT) was measured to assess whether the voles had detected and responded to predator feces as a physiological stressor. Voles of both sexes had higher levels of fecal CORT in the groups exposed to weasel feces compared to controls. Voles responded to the predator feces in a sex- and concentration-dependent manner. Males responded to LC feces by gaining less mass following the change in photoperiod. This was mediated by reduced FI and higher DEE. Female voles also gained less BM in response to HC feces, but increased both FI and DEE. We hypothesize that males may gain a short-term advantage by lowering BM in response to predation risk, which may be regained without affecting reproductive success. The consequences of mass loss in females may be more significant as this may delay the onset of breeding or reduce the size or number of young, thereby negatively affecting breeding success.     

A new method for sexing Oriental White Storks

ABSTRACT.   For species where males and females are monomorphic, or nearly so, determining the sex of individual birds generally requires either capturing birds or collecting samples, such as feathers, for DNA analysis. We developed a new method, involving the use of photographs, to determine the sex of endangered Oriental White Storks ( Ciconia boyciana ). Using photographs, we analyzed the lateral features of the heads of 25 captive storks of known sex (12 males and 13 females) and found differences between males and females in the distance from the bill tip to the nape and the distance from the bill tip to the commissural point. These differences were used to generate a discriminant function that was then tested on 22 captive storks at Hyogo Homeland Park (Toyooka, Japan), and we correctly determined the sex of 18 individuals (82%). In addition, the sex of two wild storks was correctly assigned. Our results suggest that good-quality photographs can be useful for determining the sex of both captive and wild Oriental White Storks and, further, that similar methods may prove useful for determining sex in other species of birds.     

Body protein does not vary despite seasonal changes in fat in the White Stork Ciconia ciconia

To understand how a large soaring bird, the White Stork Ciconia ciconia , copes with energy constraints, we compared changes in body mass in 14 captive adult storks with the body composition of 12 free-ranging adult storks found dead from accidents. The captive storks, already in an enclosure for several years, were fed ad libitum . They were weighed daily for 1.53.5 years using an automatic device. The bodies of the accidentally killed storks were analysed to determine total water, lipid, protein and ash contents, and to assess the biochemical composition of certain organs. Females were on average 20% lighter and 24% smaller than males, but the body mass of the sexes varied in parallel throughout the year. Body mass peaked in December and January (2530% above minimal body mass), due essentially to large fat stores in subcutaneous and abdominal adipose tissues. Body mass and body lipid rapidly decreased from February to June, whether the storks reared chicks successfully or not, and remained minimal for a few days into July. In contrast to birds using flapping flight, no variation in body protein or pectoral muscle protein was observed while breeding, even though the moult occurred then, nor in August, before the time when wild storks migrate. An endogenous regulation of body fuels is discussed.     

Annual cycle of energy and time expenditure in a golden-mantled ground squirrel population

Summary We have analyzed seasonal shifts of energy and time allocation in a population of golden-mantled ground squirrels (Spermophilus saturatus) by directly measuring total daily energy expenditure (DEE) with an isotopic technique (doubly labeled water=dlw), and by estimating components of total DEE through an integration of field behavioral observations with laboratory-measured rates of energy expenditure (oxygen consumption) associated with major behavioral and physiological states. Hibernation laster about 7 1/2 months, and the 4 1/2-month activity season consisted of mating, a 28-d gestation of 3–5 young, 5 1/2 weeks of postnatal growth building to a peak in lactation just before the young emerged above ground, an additional 2–3-week period of maternal care before dispersal, and finally restoration of body mass preceding hibernation. Although the hibernation season comprised nearly two-thirds of the year, it involved only 13–17% of annual energy expenditure, leaving about 85% of energy expenditure for the active season. Ground squirrels were actually present on the surface for only about 11% of the year's time, and the foraging time required to obtain the total annual energy supply amounted to only about 2% of the year's time. The squirrels fed mainly on herbs in the early season and hypogeous fungi later; both were used extensively during peak lactation when female energy expenditure and demand were maximal. Average daily foraging time increased steadily throughout the season to a maximum of 28% of aboveground time as availability of greens diminished and fungus predominated in the diet; time availability did not limit foraging since the animals sat on average for 65% of the daily surface time of about 7 h. Timing of reproduction is apparently optimized such that peak reproductive energy demands are matched with maximal food availability and moderate thermal conditions that minimize energy demand. Despite the greater body mass of males, the greatest total DEE (measured by dlw) of any squirrels at any time of year was that of females during peak lactation. For production of young and lactation through above-ground emergence of an average litter of 2.7, females required a total energy increase of 24% above annual nonreproductive metabolism. Yearling females all bred and performed similarly to older females, yet some costs were greater because the yearlings began and ended hibernation at smaller mass, compensated by giving birth later, and finally showed a greater absolute increase in body mass over the active season than older females. Annual metabolic energy expenditure of breeding males was about 18% greater than that of females, due to greater male body mass. Yet the annual energy intake requirement for both sexes was essentially identical (about 42MJ) due to the greater reproductive export by females in the form of newborn and milk. During the mating season males showed wide-ranging exploratory behavior and social interactions, including aggression, that involved considerable locomotory energy expenditures. Although we did not directly account for the energetics of these specific reproductive behaviors, they are critical to male reproductive success and on a daily basis they probably involved much greater energy expenditure than sperm production. Some yearling males avoided these costs by foregoing testicular development, yet they allocated four times as much energy to growth as older males, thereby increasing somatic condition for the future.     

Seasonal pattern in age, sex and body condition of Barn Owls Tyto alba killed on motorways

The Barn Owl Tyto alba was the most common owl killed on motorways in northeastern France. The possible causes of this mortality and the age, sex and body condition of the road-killed birds in 1991–1994 have been investigated. The number of birds killed on roads was highest in the period from early autumn to late winter, i.e. during the non-breeding period, and showed a pattern similar to that of the temporal difference between sunset, which varies with day length, and peak of traffic, the occurrence of which is constant throughout the year. An autumnal mortality peak, concomitant with the post-fledging dispersal, was mainly of immature birds, especially females. A second mortality peak in late winter was composed mainly of mature birds, with an equal proportion of males and females. From autumn to winter, there was no significant change in body mass in the different age and sex categories of birds killed on roads, except for mature males which had a significantly lower body mass in winter. From early autumn to late winter, the mean body mass of immature owls killed on motorways did not differ significantly from that of captive immatures fed ad libitum. This suggests that the immature birds were in good body condition. In contrast, the body mass of road-killed mature females was significantly lower than that of captive mature females over the same time periods. In mature males in late winter, a drop in body mass in both road-killed and captive birds suggests an endogenous seasonal phenomenon. Except for mature females, Barn Owls killed on roads in 1991–1994 were in good body condition. This does not support the idea that only birds in poor body condition were killed. We conclude that the mortality of Barn Owls on motorways in autumn and winter was probably related to the concomitance between the peak of traffic and the onset of hunting activity and the large number and dispersal of immature individuals during the same period.     

The energy costs of sexual dimorphism in mole-rats are morphological not behavioural

Different reproductive strategies of males and females may lead to the evolution of differences in their energetic costs of reproduction, overall energetic requirements and physiological performances. Sexual dimorphism is often associated with costly behaviours (e.g. large males might have a competitive advantage in fighting, which is energetically expensive). However, few studies of mammals have directly compared the energy costs of reproductive activities between sexes. We compared the daily energy expenditure (DEE) and resting metabolic rate (RMR) of males and females of two species of mole-rat, Bathyergus janetta and Georychus capensis (the former is sexually dimorphic in body size and the latter is not) during a period of intense digging when males seek females. We hypothesized that large body size might be indicative of greater digging or fighting capabilities, and hence greater mass-independent DEE values in males of the sexually dimorphic species. In contrast to this prediction, although absolute values of DEE were greater in B. janetta males, mass-independent values were not. No differences were apparent between sexes in G. capensis. By comparison, although RMR values were greater in B. janetta than G. capensis, no differences were apparent between the sexes for either species. The energy cost of dimorphism is most likely to be the cost of maintenance of a large body size, and not the cost of behaviours performed when an individual is large.     

Sexual dimorphism in the energetics of reproduction and growth of North Sea plaice, Pleuronectes platessa L.

The chemical composition and energy content of North Sea plaice during the spawning period were examined in mature males and females and in immature fish, to study differences in the allocation of energy over reproduction and somatic growth between the sexes. At the beginning of the spawning period mature males and females had equal dry weights of lipid that were 70% higher than in immatures. Protein content in mature males was equal to that in immatures but was 23 % higher in mature females. Immature males and females did not differ in chemical composition. At the end of the spawning period, spent and immature fish had equal lipid contents, but protein content in spent females was 10% lower than in spent males, and 17% lower than in immatures. Gross energy content of the body decreased by 44% (65·2 to 36·3 J cm^-3) in mature females, 27% (55·0 to 40·OJ cm^-3) in mature males, and 9% (48·7 to 44·2J cm^-3) in immatures. Energy content of plaice eggs was estimated at 6·60 kJ per 1000 eggs. Reproductive investment was estimated from the energy loss during the spawning period and included the energy of sex products and spawning metabolism. Somatic growth comprised the annual increase in energy content of fish. The pattern of energy allocation over reproduction and somatic growth differed between males and females. Males started their reproduction at a smaller length and a younger age and allocated a higher proportion of the available energy into reproduction than females. Available energy resources for somatic growth and reproduction (surplus production) were equal between the sexes up to a length of about 30 cm. Beyond this length male surplus production levelled off whereas female surplus production continued to increase. The differences in surplus production and the allocation patterns are discussed. For female plaice the energy allocated into egg production was estimated as between 48 and 64% of the total amount of energy lost during spawning. The remaining energy is used for metabolism during the spawning period, yielding an estimate of the metabolic rate of mature females of between 6·4 and 9·1 kJ day^-1. A maximum estimate of the metabolic rate of mature males was 7·4 kJ day^-1.     

Seasonal sex–specific energy expenditure in breeding and non-breeding Palestine sunbirds Nectarinia osea

The timing of the chick‐rearing phase is known to have a profound effect on the reproductive success of birds. However, little is known about the energetic costs faced by the parents during different periods of the breeding season. These costs may have vital consequences for both their survival and future reproduction. In most studies, daily energy expenditure (DEE) of breeding and non‐breeding birds has been compared, without controlling for the effect of season. In the present study, we examined the energy demands of breeding compared to non‐breeding Palestine sunbirds Nectarinia osea and whether there were sex‐specific differences in DEE within and between different seasons. We predicted that DEE would be elevated when birds rear chicks, especially at cooler ambient temperatures. Time‐energy budgets were constructed for pairs of sunbirds, rearing chicks, or not breeding, in spring and summer. There were significant seasonal differences in estimates of DEE in non‐breeders that were 21% higher in spring than in summer. We attributed these to increases in non‐flight metabolic rate rather than changes in time spent on different activities. Our estimates of DEE for the birds that were rearing chicks were higher than non‐breeding adults. In females the increase in DEE when breeding, compared to when not breeding, was similar in both spring and summer, while males increased their DEE much less when breeding in spring. The differences in estimated DEE, however, were not significant between male and female birds in any season. Between seasons, female breeders had 17.1% higher DEE in spring than in summer, while male breeders showed no difference in DEE when rearing chicks in different seasons. Accordingly, our initial prediction was supported, as DEE in chick‐rearing adults was higher than in non‐breeding adults. In addition, although temperatures are lower in spring, breeding in the spring is only more costly than breeding in summer for females. Apparently, males are more flexible in reallocating their time and energy spent on different activities.     

Annual cycles in moult, body mass, luteinizing hormone, prolactin and gonadal steroids during the development of sexual maturity in the White stork (Ciconia ciconia)

Annual variations in moult, body mass, and the plasma concentrations of luteinizing hormone, prolactin and the gonadal steroids, oestradiol and testosterone, were measured in captive White storks ( Ciconia ciconia ). Data were collected at approximately monthly intervals for 13 months on storks hatched over five successive years, the youngest ones being in their first, the oldest in their fifth, year of life.
Moulting of wing feathers occurred during the summer months, April through August. Young birds began to moult at least one month earlier, and replaced more wing feathers each year, than did three- to five-year-old birds. Body mass exhibited remarkably consistent annual cycles with minima of2–9-3-5 kg, during the summer months, and maxima of3–8-4-5 kg, during the winter months. Young males were heavier at all times of the year than young females, although this difference was gradually reduced to non-significant levels by four years of age. Luteinizing hormone, prolactin and the gonadal steroids, oestradiol and testosterone, exhibited annual cyclic changes, usually of a bi-modal nature. No major differences in hormone profiles, however, were found between any of the age groups. The phenomenon of deferred maturity in the stork does not parallel that of puberty found in many mammals.     

不同性别和年龄的大仓鼠对黄鼬气味的反应

将雌性成体和雌雄亚成体大仓鼠 (Cricetulustriton)长期 (4周 )暴露给过量的黄鼬 (Mustelasibirica)肛腺分泌物 ,观察其行为和生理状态的变化 ,并通过与我们以前有关黄鼬气味对成年雄鼠影响的研究结果进行比较 ,表明黄鼬气味对不同性别和不同年龄大仓鼠的胁迫效应和生殖抑制存在差异。发现黄鼬气味对雌性大仓鼠的影响较雄性小 ,对亚成体的影响较成体小 ,这与雌性和未成年动物对各种胁迫因素的反应更敏感的普遍现象相反。在成年鼠中 ,雌雄鼠的攻击行为都受到黄鼬气味的抑制 ;但天敌气味使雌性的胁腺膨大 ,对胁腺标记和肾上腺大小无影响 ;成年雄鼠的肾上腺膨大 ,胁腺萎缩 ,标记减少。在亚成体中 ,除了雄性胁腺受到抑制(与成年雄鼠相同 )外 ,雌雄鼠的肾上腺和雌性的胁腺未受影响。亚成体实验鼠的体重都比对照组低 ,但成年鼠的体重未受影响。另外 ,与以往对其它鼠类的研究结果一致 ,天敌气味并不影响成年鼠的生殖器官 ,却抑制了未成年雄鼠的附睾和未成年雌鼠的子宫。这些差异可能和生理基础的性二态以及可能面临的被捕食风险大小有关     

Seasonal changes in thermogenesis and body mass in wild Mongolian gerbils (Meriones unguiculatus)

Seasonal adjustments in body mass (BM), nonshivering thermogenesis (NST) and several physiological, hormonal, and biochemical markers were measured in wild-trapped Mongolian gerbils (Meriones unguiculatus) from Inner Mongolia, China. Sexual differences were detected in BM, NST, brown adipose tissue (BAT) mass, and mitochondrial protein content. BM and NST in males were higher in winter (January) and spring (May) than in summer (August), and BM of females was also the highest in winter, but NST remained relatively constant throughout the year. Cytochrome c oxidase activity and mitochondrial uncoupling protein 1 (UCP1) content in BAT were enhanced in winter in males or females, respectively. Serum leptin concentration was the lowest in winter and positively correlated with BM and body fat mass but was negatively correlated with BAT UCP1 content. These data suggest that wild Mongolian gerbils do not depend on a decrease in BM, but instead increase their thermogenic capacity to cope with cold stress. Leptin may be involved in the seasonal regulation in energy balance and thermogenesis in field Mongolian gerbils.     

Evidence for a trade-off between growth and body reserves in northern white-tailed deer

We contrasted patterns of growth and accumulation of body reserves in autumn between two high-density (HD) white-tailed deer populations facing winters of different severity and length. Both populations occurred in the absence of effective predators and suffered from some forage competition based on reduced body masses. A third population living at low density (LD) and confronting long and severe winters (SW) served to distinguish the influence of food competition and winter severity on growth and body reserves. We estimated body components (water, protein, fat and ash) of deer during the first half of November and compared growth patterns between sexes and regions. HD-SW males continuted growth to an older age than HD males facing short and mild winters (MW) but females of both regions reached adult body mass at the same age. LD-SW deer exhibited a growth pattern similar to that of HD-SW animals but were the heaviest and the largest, suggesting that growth patterns are related to winter harshness (or length of the growing season) and that final body size is related to forage competition in summer. Sexual dimorphism became evident at an older age in the HD-SW population than in the HD-MW population, demonstrating that winter harshness does not affect immature males and females in the same manner. Fawns from the HD-SW population had proportionally longer legs and a higher percentage of body fat. Adaptations of immature deer to long and severe winters suggest that survival during the first winter represents the most critical step in the life span of northern white-tailed deer.     

Impact of body reserves on energy expenditure, water flux, and mating success in breeding male northern elephant seals

In capital breeders, individual differences in body size and condition can impact mating effort and success. In addition to the collateral advantages of large body size in competition, large nutrient reserves may offer advantages in endurance rivalry and enable the high rates of energy expenditure associated with mating success. We examined the impacts of body reserves and dominance rank on energy expenditure, water flux, mating success, and breeding tenure in the adult male northern elephant seal, a polygynous, capital breeder. Adult males expended energy at a rate of 159 ± 49 MJ d (-1), which is equivalent to 3.1 times the standard metabolic rate predicted by Kleiber's equation. Despite high rates of energy expenditure and a long fasting duration, males spared lean tissue effectively, deriving a mean of 7% of their metabolism from protein catabolism. Body composition had a strong impact on the ability to spare lean tissue during breeding. When controlling for body size, energy expenditure, depletion of blubber reserves, and water efflux were significantly greater in alpha males than in subordinate males. Large body size was associated with increased reproductive effort, tenure on shore, dominance rank, and reproductive success. Terrestrial locomotion and topography appeared to strongly influence energy expenditure. Comparisons with conspecific females suggest greater total seasonal reproductive effort in male northern elephant seals when controlling for the effects of body mass. In polygynous capital breeding systems, male effort may be strongly influenced by physiological state and exceed that of females.     

长爪沙鼠免疫功能、体脂含量和器官重量的季节变化

小型哺乳动物的体脂含量与免疫功能有关,并受环境条件的影响。为了进一步理解野生长爪沙鼠对环境的生存适应策略,我们于2004 年夏季(7～8月)和2005年冬季(1～3月)测定了野生长爪沙鼠的体重、体脂含量和脏器重量,以及由匙孔血蓝蛋白(KLH)对雄鼠所介导的体液免疫反应。结果发现:雄鼠的胴体干重和体脂含量都显著高于雌鼠,其他各项指标无性别差异。冬季雌雄沙鼠的体重、胴体干重、体脂含量和褐色脂肪组织的湿重,以及雄鼠的睾丸湿重都显著高于夏季。脾脏的重量冬季趋于降低。处理组(注射KLH )动物血清中抗KLH 抗体的含量在冬季和夏季都显著高于对照组(注射生理盐水),且冬季处理组显著高于夏季处理组。本研究结果为动物种群调节的“冬季免疫增强假说”提供了一个新的野外例证。没有检测到免疫器官和产热器官、免疫器官和繁殖器官之间的权衡关系。     

Energy expenditure during egg laying is equal for early and late breeding free-living female great tits

In many bird populations, variation in the timing of reproduction exists but it is not obvious how this variation is maintained as timing has substantial fitness consequences. Daily energy expenditure (DEE) during the egg laying period increases with decreasing temperatures and thus perhaps only females that can produce eggs at low energetic cost will lay early in the season, at low temperatures. We tested whether late laying females have a higher daily energy expenditure during egg laying than early laying females in 43 great tits (Parus major), by comparing on the same day the DEE of early females late in their laying sequence with DEE of late females early in their egg laying sequence. We also validated the assumption that there are no within female differences in DEE within the egg laying sequence. We found a negative effect of temperature and a positive effect of female body mass on DEE but no evidence for differences in DEE between early and late laying females. However, costs incurred during egg laying may have carry-over effects later in the breeding cycle and if such carry-over effects differ for early and late laying females this could contribute to the maintenance of phenotypic variation in laying dates.     

Energy expenditure and testosterone in free-living male yellow-pine chipmunks

The onset of mating in yellow-pine chipmunks (Tamias amoenus) follows emergence from a prolonged period of energy conservation during hibernation. Energy expenditures are greatly accelerated to meet the demands of the reproductive season. When emerging from hibernation, typical male chipmunks (breeders) have enlarged testes and a high level of plasma testosterone (T). However, certain males that do not participate in reproduction (nonbreeders) maintain small testes and low plasma T levels and emerge several weeks later than the breeders. The timing of the terminal arousal from hibernation and onset of mating are associated with increased plasma T levels. Experimental elevation of T levels in T. amoenus outside the mating season has been associated with a decrease in body mass, further suggesting an effect of T on energy balance. To test this hypothesis, we measured daily energy expenditure (DEE) in free-living, nonbreeding male chipmunks in the presence and absence of a T-implant. We also measured DEE in breeding males when endogenous T levels were high. DEE of the nonbreeders was not affected by our manipulation of plasma T, and the DEE of breeding males did not differ from that of nonbreeders. We conclude that energy expenditure on a daily basis in male yellow-pine chipmunks is not influenced by levels of T. However, on a seasonal basis, the earlier emergence from hibernation by breeding males, which appears to be influenced by T, represents an overall seasonal energy expenditure that exceeds that of nonbreeding males.     

Cost of living in free-ranging degus (Octodon degus): seasonal dynamics of energy expenditure

Animals process and allocate energy at different seasons at variable rates, depending on their breeding season and changes in environmental conditions and resulting physiological demands. Overall total energy expenditure, in turn, should either increase in some seasons due to special added demands (e.g. reproduction) or it could simply remain at about the same level, in which case the animals must show compensatory rebalancing of other expenditures that can be reduced. To test for the alternative hypotheses of seasonal variability or compensation, we measured total daily energy expenditure (DEE) in free-living degus (Octodon degus) at four seasons and followed this with determinations of basal metabolic rate (BMR) in the laboratory in the same individuals. DEE varied seasonally but was only significantly different (lower) in summer (non-breeding season), with a DEE:BMR ratio of only 1.6, whereas autumn, winter and spring DEE values were statistically indistinguishable from one another and showed DEE:BMR ratios ranging from 1.9 to 2.2. Our values of DEE in the field fall within the broad range of allometric expectation for herbivorous mammals in general, but the ratios of DEE:BMR are lower than expected. This, together with the lack of strong major shifts in total levels of DEE, suggests that degus are showing compensatory shifts among various categories of energy expenditure that allow them to manage their overall energy balance by minimizing total expenditure.     

Seasonal and developmental changes of reproductive organs of male ringed seals (Phoca hispida) in the Svalbard area

The weights of testes, prostate gland and baculum of ringed seal males were related to age, season and differences in body size. There was a significant seasonal variation in testes and prostate gland size of sexually mature males, with a maximum occurring in early April. There were no seasonal changes in prostate weight of immature males, but some of the older immatures had elevated testes weights in April. Testes weight was significantly correlated with lean body mass. The increase in testes size with increasing body weight was greater for seals six years of age or older than for younger males. We suggest that some testicular growth and a seasonal cycle in testes growth occur before the testes become functional endocrinologically. We also believe that the primary event leading to puberty in ringed seals is an age-dependent shift in metabolic processes, directing a larger percentage of available energy towards the reproductive organs.