Population parameters and harvest risks for polar bears (<Emphasis Type="Italic">Ursus maritimus</Emphasis>) of Kane Basin,Canada and Greenland

We estimated demographic parameters and current harvest risks for a population of polar bears (Ursus maritimus Phipps) inhabiting northern Smith Sound and Kane Basin, Canada and Greenland. Our demographic analysis included a detailed assessment of age- and sex-specific survival and recruitment from 141 marked polar bears, using information contained within the standing age distribution of captures and mark-recapture analysis. Total survival rates for females were: 0.374 ± 0.180 (cubs), 0.686 ± 0.157 (ages 1–4), and 0.967 ± 0.043 (ages 5+). Mean litter size was 1.67 ± 0.08 cubs. Females did not reproduce until at least age 6, which is late compared to other populations of polar bears. The model-averaged, mark–recapture estimate of mean abundance (±1 SE) for years 1994–1997 was 164 ± 35 bears. We incorporated demographic parameters and their variances into a harvest risk analysis (i.e., a stochastic, harvested population viability analysis, PVA). Results suggest that polar bears in the region were severely over-harvested during the mark–recapture interval (1992–1997). The current status of the population is unknown.     

HAS THE AGE AT TRANSITION OF SOUTHERN HEMISPHERE MINKE WHALES DECLINED OVER RECENT DECADES?

The earplugs of several baleen whale stocks exhibit seasonal growth layers which have been shown for some species to indicate the total age of the animals. A transition from early, irregular layers, to later, more regular layers can be seen in these earplugs, and this is thought to indicate the age at maturity of the whale. The earplugs of Southern Hemisphere minke whales are relatively difficult to read, particularly for the age at transition, and it has been suggested that these readings reflect no more than random allocations by the reader, rather than any real effect. Plots of average transition phase against year of birth (cohort) show a decline in the average age at transition. However, certain factors can result in a downward bias in this trend, particularly when only a short time-series is available for analysis, as was the case when this trend was first estimated some 15 yr ago. Data collected over 25 yr are now available and are reanalyzed here. A plot of mean age at transition against year of sampling for animals of similar age shows a decline, as does the conventional plot against cohort, suggesting that the decline is real. A model that simulates random allocation of the transition phase by earplug readers yields predictions that show systematic deviations from the data. In contrast, a second model that allows for a real trend in the average age at transition and that takes account of two potentially biasing effects (termed truncation and the fringe effect) fits the data well. A tendency is evident for readers to recognize a transition phase in a greater proportion of the earplugs that they read as they gain experience over time. This is taken into account in the model. This model shows a decline in the average age at transition from roughly 11 for the cohorts of the 1950s to roughly 7 for those of the 1970s. These results suggest that minke whale transition-phase readings are related to a real signal in the data and are not simply an artefact, and further that there has been a real decline in the age to which this signal corresponds.     

Longevity and life history of cave bears – a review and novel data from tooth cementum and relative emergence of permanent dentition

Abstract

Longevity and other life history variables are key to understanding evolutionary processes and the biology of extinct animals. For the past 20 years, the lifespan of cave bears received an increased interest. Studies focusing on incremental lines of tooth cementum resulted in detailed mortality patterns from different localities. In this review, we summarise literature on age estimation as well as mortality of different European cave bear localities and present novel data on longevity from 94 teeth originating from 20 European localities. Additionally, the relative tooth emergence pattern of the permanent dentition is investigated under the Schultz’s rule framework of possible life history implications. For this, the known sequences of extant bear species are compared with the one of cave bears. Our results suggest that the typical duration of the life of cave bears was 19 years but data from literature show that in rare cases ages of up to 30–32 years were achieved. Additionally, we present the oldest known age for the Middle Pleistocene cave bear Ursus deningeri, 29 years. The tooth eruption pattern of cave bears exhibits a heterochronic shift that implies, under the assumption of Schulz’ rule, a slightly faster life history than closely related species.     

Spatial and temporal patterns of problem polar bears in Churchill,Manitoba

Human–bear interactions near the town of Churchill, Manitoba occur annually because the Western Hudson Bay polar bear population spends 4–5 months on-land each year when the sea ice melts completely. Significant changes have occurred in the Hudson Bay ecosystem and in the bear population as a result of climate warming; however, how these changes may have influenced human–bear interactions near Churchill is unclear. This study examined the temporal and spatial patterns of 1,487 problem bears captured in the Churchill area from 1970 to 2004. We also examined the relationship between problem bears and environmental variables as well as the Nunavut harvest. The number of individual problem bears caught near Churchill varied from 10 to 90 individuals per year and increased over time. Subadult males comprised 39%, subadult females 23%, adult males 18%, females with young 14%, and solitary females 6% of captures. Bears that became problem individuals were in closer proximity to the Churchill area. Nutritional stress and a northward shift in the distribution of the bears that spend the summer on-land in northeastern Manitoba may account for the increase in problem bear numbers. The date of sea ice freeze-up, which is getting progressively later, was the best predictor explaining the annual variation in the occurrence of problem bears. These results provide an understanding of how a warming climate may directly impact polar bear behaviour. This information may allow wildlife managers to predict relative levels of human–bear interactions and thereby implement effective management strategies to improve human safety and the conservation of polar bears.     

Plasma biochemical values from apparently healthy free-ranging polar bears from Svalbard

To establish reference values for free-ranging polar bears (Ursus maritimus) at Svalbard, Norway, plasma samples from 15 females and 20 males were analyzed for 28 blood biochemistry parameters. Animals were chemically immobilized (Zoletil: tiletamine and zolazepam) on land at Barents?ya, Edge?ya, and the eastern coast of Spitsbergen in August 1998. All bears were apparently healthy, with ages ranging from 1-22 yr. Females had almost two times higher levels of lipase than males. Several parameters varied with age. Levels of alkaline phosphatase (ALP) and calcium (Ca) decreased with age, being significantly higher in young individuals (< 6 yr) compared to middle-aged (6-13 yr) and older bears (> 13 yr). Globulin was lower in animals < 6 yr of age than in animals > 13 yr of age, while the opposite was the case for albumin. Levels of ALP, Ca, and potassium decreased with age. We found no significant changes in total protein correlated to age, but total protein levels were higher in obese compared to lean individuals. Further, total protein levels were slightly lower and had greater variation compared to data from polar bears in captivity, which may reflect food availability for the latter group. The mean ratio between urea and creatinine was 10.9 and indicated these bears were fasting. These data provide a baseline from which to compare biochemical parameters in captive and free-ranging polar bears and will be especially valuable for future studies of polar bears at Svalbard.     

The method of age determination of the Pacific walrus (Odobenus rosmarus divergens) using the layered structure of functional teeth

The functional teeth of Pacific walruses that died or were harvested in the Retkyn Spit, Enmelen village, Kolyuchin Island, Vankarem Cape, Enurmino village, and Chegitun River region in 2005, 2007–2008, and 2010–2011 were examined. The definite structure was investigated in animals of their first year of life. The presence of a milk layer in the tooth dentine can be considered as a mark that all the cement layers have been preserved, and the age determination of an individual is precise. The annual increment of dentine significantly changed with age in different parts of the tooth (buccal, lingual, and central), and the annual growth of dentine decreased every year. The growth rate of the upper jaw teeth was significantly higher, and the duration of their growth was much longer than that in the lower jaw teeth. The wearing of dentine and cement layers was unequal in different parts of tooth. Several recommendations for choosing a tooth for the determination of the walrus’s age and for the estimation of age using the layered tooth structure are given.     

Observations of mortality associated with extended open-water swimming by polar bears in the Alaskan Beaufort Sea

During aerial surveys in September 1987–2003, a total of 315 live polar bears were observed with 12 (3.8%) animals in open water, defined for purposes of this analysis as marine waters >2 km north of the Alaska Beaufort Sea coastline or associated barrier islands. No polar bear carcasses were observed. During aerial surveys in early September, 2004, 55 polar bears (Ursus maritimus) were seen, 51 were alive and of those 10 (19.9%) were in open water. In addition, four polar bear carcasses were seen floating in open water and had, presumably, drowned. Average distance from land and pack ice edge for live polar bears swimming in open water in 2004 (n=10) were 8.3±3.0 and 177.4±5.1 km, respectively. We speculate that mortalities due to offshore swimming during late-ice (or mild ice) years may be an important and unaccounted source of natural mortality given energetic demands placed on individual bears engaged in long-distance swimming. We further suggest that drowning-related deaths of polar bears may increase in the future if the observed trend of regression of pack ice and/or longer open water periods continues.     

Hematology of Southern Beaufort Sea Polar Bears (2005–2007): Biomarker for an Arctic Ecosystem Health Sentinel

Arctic temperatures are increasing in response to greenhouse gas forcing and polar bears have already responded to changing conditions. Declines in body stature and vital rates have been linked to warming-induced loss of sea-ice. As food webs change and human activities respond to a milder Arctic, exposure of polar bears and other arctic marine organisms to infectious agents may increase. Because of the polar bear’s status as arctic ecosystem sentinel, polar bear health could provide an index of changing pathogen occurrence throughout the Arctic, however, exposure and monitoring protocols have yet to be established. We examine prevalence of antibodies to Toxoplasma gondii, and four morbilliviruses (canine distemper [CDV], phocine distemper [PDV], dolphin morbillivirus [DMV], porpoise morbillivirus [PMV]) including risk factors for exposure. We also examine the relationships between antibody levels and hematologic values established in the previous companion article. Antibodies to Toxoplasma gondii and morbilliviruses were found in both sample years. We found a significant inverse relationship between CDV titer and total leukocytes, neutrophils, monocytes, and eosinophils, and a significant positive relationship between eosinophils and Toxoplasma gondii antibodies. Morbilliviral prevalence varied significantly among age cohorts, with 1–2 year olds least likely to be seropositive and bears aged 5–7 most likely. Data suggest that the presence of CDV and Toxoplasma gondii antibodies is associated with polar bear hematologic values. We conclude that exposure to CDV-like antigen is not randomly distributed among age classes and suggest that differing behaviors among life history stages may drive probability of specific antibody presence.     

Reproductive biology and ecology of female polar bears (Ursus maritimus)

Data on age-specific natality rates, litter size, interbirth interval, age of first reproduction, reproductive senescence, age of weaning and cub survival were determined for a free-ranging population of polar bears inhabiting Hudson Bay, Canada, near the southern limit of the species range. Serum progesterone levels were also determined for females at different stages of their reproductive cycle to provide corroborative support for the reproductive parameters described. Animals were live captured using immobilizing drugs and each animal uniquely marked for future identification. First parturition occurred at four or five years of age and the age-specific natality rate increased with age until approximately 20 years, after which it dropped markedly. At least 40% of adult females displayed two-year interbirth intervals and 55% of cubs in their second year were independent of their mother. Mean size of cub litters in spring was 1.9 and 13% of litters had three or more cubs. The natality rate for 5–20-year-old females was estimated as 0.9, higher than that reported for any more northerly polar bear populations where two-year interbirth intervals are rare, fewer than 5% of yearling cubs are weaned and triplet litters occur with less than 1% frequency. Cub mortality was initially high and declined with age. Although cubs in western Hudson Bay were weaned at a younger age and a lighter weight than their counterparts in more northern populations, cub mortality rates were similar. The reason for the marked differences in reproductive parameters in the western Hudson Bay population is not known. We speculate that sea-ice conditions may be sufficiently different to allow weaned bears at a lighter body weight to hunt seals more successfully there than further north.     

Fasting physiology of polar bears in relation to environmental change and breeding behavior in the Beaufort Sea

We examined the use of the ratio of serum urea to serum creatinine as a physiological biomarker of fasting to monitor temporal patterns in the feeding ecology of polar bears (Ursus maritimus). Blood was collected from 436 polar bears in the eastern Beaufort Sea during April and May of 1985–1986 and 2005–2006. The proportions of polar bears fasting were 9.6% in 1985, 10.5% in 1986, 21.4% in 2005, and 29.3% in 2006. We used stepwise logistic regression analysis to evaluate factors that could influence the binary response variable of fasting or not fasting. Significant predictor variables of fasting were: the 2005 and 2006 capture years, solitary adult male bears, and adult male bears that were accompanying an estrous female. The increased number of polar bears in a physiological fasting state from all sex, age, and reproductive classes in 2005 and 2006 corresponded with broad scale changes in Arctic sea ice composition, which may have affected prey availability. The higher proportion of adult males fasting from all years was attributed to spring breeding behavior.     

Differences in growth,size and sexual dimorphism in skulls of East Greenland and Svalbard polar bears (<Emphasis Type="Italic">Ursus maritimus</Emphasis>)

Size, growth and sexual dimorphism of nine skull traits was studied in 300 East Greenland and 391 Svalbard polar bears (Ursus maritimus). Two traits were significantly larger in bears from East Greenland compared to Svalbard bears, and trait size was smaller after 1960 in five traits. For both localities and both age groups (subadult, adult), mean trait size values were higher in males than females (all: P < 0.05). Gompertz growth models showed trait size increasing with age in seven traits. Depending on the trait, males reached 95% asymptotic trait size at age 3–10, females at age 2–6. The females of both localities matured at approximately the same age, whereas the Svalbard males generally matured years later than their East Greenland peers. The differences found in the present study between the two polar bear subpopulations support the notion that East Greenland and Svalbard polar bears probably should be managed as separate units.     

Field age determination of leopards by tooth wear

Age determination is an important tool in wildlife studies. Estimating the age of animals in the field using tooth wear criteria may be subject to error as a result of variations between individuals, habitats and populations. Data on age estimation of leopards and tooth wear characteristics are lacking. Nineteen leopards in Namibia were assessed for tooth eruption and wear. Between 1991 and 1995 leopards (including 13 individuals of known age) were monitored at one year intervals ('28 leopard years') to record age and tooth wear. At the age of two years leopards had fully developed dentition. Wear started with the incisors and canines, and spread to the premolars and molars. A chronology of tooth eruption and wear in relation to age is presented. Above the age of three years, male leopards showed higher frequencies of enamel flaking and canine fractures than females.     

Does rumen–reticulum capacity correlate with body size or age in black-tailed deer?

To accommodate an increased food intake with greater body size, rumen–reticulum capacity must become larger to allow heavier digesta loads. Recently, digesta load was found to correlate with age more strongly than body size. It was suggested that older animals had compromised mastication efficiency due to tooth wear and compensated for larger particles by increasing rumen–reticulum capacity to extend retention time. Herein, we constructed models and used Akaike Information Criteria corrected for small sample size to determine if digesta load was related with age or body weight in 80 female and 105 male black-tailed deer (Odocoileus hemionus columbianus). We also assessed if the presence of fetuses influenced relationships in females. Females were collected in spring, 1985–1988, and males were collected in autumn, 1980, 1982–1984, and 1988, from Hopland Research and Extension Center, Mendocino County, California. Digesta loads, fetuses, and carcasses were weighed, and animal ages were estimated. Digesta load was related to age in females and body weight in males. Our study shows that body size and age-related factors may both influence rumen–reticulum capacity.     

Antibodies to canine distemper and phocine distemper viruses in polar bears from the Canadian arctic

Serum samples collected from 200 polar bears (Ursus marititnus) from two populations in the Canadian arctic, the western Hudson Bay and Lancaster Sound populations, between 1989 and 1996, were tested for antibodies to canine distemper (CDV) and phocine distemper viruses (PDV) using virus neutralization. Antibodies to CDV and PDV were detected in 48 and six polar bears, respectively. All six bears that tested positive for PDV also tested positive for CDV; in only one case did the antibody titer for PDV exceed that of CDV. Differences in antibody prevalence to CDV were detected between populations and age classes but not sex or year of sampling.     

Short-term behavioural response of polar bears (<Emphasis Type="Italic">Ursus maritimus</Emphasis>) to snowmobile disturbance

In this study the distance, at which polar bears detected and actively responded to approaching snowmobiles was measured and the behavioural response was recorded. The study was performed on Svalbard, an arctic island where human traffic has increased substantially in recent years. Fieldwork was conduced in April and/or May during the years 2003–2005. Polar bears were observed on ice with telescopes and binoculars. Undisturbed polar bears were observed continuously and their behaviours recorded, during the time when two snowmobiles moved toward the bear(s). Distances between the bear, the observer, and the approaching snowmobiles were measured using GPS positions taken on the track towards the bear. Data on the behavioural response of 20 encounters with bears were collected. On average, bears were alerted to the snowmobiles at 1,164 m. Mean distance at which the locomotive response occurred was 843 m, and there was a statistical significant difference in distance between sex and age classes [326 m (95% CI = 138–496 m) for adult males; 1,534 m (95% CI = 508–2,768 m) for adult females with cubs; 164 m (95% CI = 49–543 m) for two adult females without cubs; and 1,160 m (95% CI = 375–1,353 m) for single medium sized bears]. The responses of the polar bears to the snowmobiles were categorized according to intensity and persistence of reactions. Females with cubs and single medium sized bears tended to show more intense responses than adult males and lone adult females. Wind direction affects sound and odour transmission, and although an effect on response distance was not found, the response intensity was affected by wind direction. We conclude that female polar bears with small cubs in particular may have a greater risk to be disturbed, since they react at greater distances with amplified reactions; thus, users of snowmobiles should take particular care in areas where females with cubs are present.     

Relationship of Tooth Wear to Chronological Age among Indigenous Amazon Populations

In indigenous populations, age can be estimated based on family structure and physical examination. However, the accuracy of such methods is questionable. The aim of this cross-sectional study was to evaluate occlusal tooth wear related to estimated age in the remote indigenous populations of the Xingu River, Amazon. Two hundred and twenty three semi-isolated indigenous subjects with permanent dentition from the Arara (n = 117), Xicrin-Kayapó (n = 60) and Assurini (n = 46) villages were examined. The control group consisted of 40 non-indigenous individuals living in an urban area in the Amazon basin (Belem). A modified tooth wear index was applied and then associated with chronological age by linear regression analysis. A strong association was found between tooth wear and chronological age in the indigenous populations (p <0.001). Tooth wear measurements were able to explain 86% of the variation in the ages of the Arara sample, 70% of the Xicrin-Kaiapó sample and 65% of the Assurini sample. In the urban control sample, only 12% of ages could be determined by tooth wear. These findings suggest that tooth wear is a poor estimator of chronological age in the urban population; however, it has a strong association with age for the more remote indigenous populations. Consequently, these findings suggest that a simple tooth wear evaluation method, as described and applied in this study, can be used to provide a straightforward and efficient means to assist in age determination of newly contacted indigenous groups.     

Age estimation and growth layer patterns in teeth of crabeater seals: A comparison of techniques

Age estimation of marine mammals provides important information about ecological and life history parameters. Counting growth layer groups (GLGs) in the dentine and cementum of teeth is the most common technique for age estimation in pinnipeds. In this study, we used acid-etched canines (n = 38) and decalcified stained postcanine sections (n = 40) to calibrate readings in mummified crabeater seals (Lobodon carcinophaga). A subsample of this group received a prior cleaning treatment of boiling the teeth with hydrogen peroxide (H₂O₂). Ages ranged from 0 to 31 years. Dentine from canines and cementum from postcanines showed higher estimated ages (maximum 31 years) than dentine from postcanines (maximum 24 years), mainly in those teeth that did not receive prior treatment. Boiling with H₂O₂ has shown to affect cementum structure and, thus, results in underestimated ages, but dentine did not seem to be affected. The results presented here showed that ages can be estimated for the crabeater seal regardless of which tooth/tissue or method is used, at least for seals <13 years old. However, nontreated, stained thin sections of postcanine teeth are recommended because more reliable age estimations in older crabeater seals are obtained.     

Demography and population viability of polar bears in the Gulf of Boothia, Nunavut

We estimated demographic parameters and harvest risks for polar bears ( Ursus maritimus ) inhabiting the Gulf of Boothia, Nunavut, from 1976 to 2000. We computed survival and abundance from capture–recapture and recovery data (630 marks) using a Burnham joint live–dead model implemented in program MARK. Annual mean total survival (including harvest) was 0.889 ± 0.179 (± 1 SE) for cubs, 0.883 ± 0.087 for subadults (ages 1–4), 0.919 ± 0.044 for adult females, and 0.917 ± 0.041 for adult males. Abundance in the last 3 yr of study was 1,592 ± 361 bears. Mean size of newborn litters was 1.648 ± 0.098 cubs. By age 7, 0.97 ± 0.30 of available females were producing litters. Harvest averaged 38.4 ± 4.2 bears/year in the last 5 yr of study; however, the 2002–2007 kill averaged 56.4 bears/yr. We used a harvested Population Viability Analysis (PVA) to examine impacts of increasing rates of harvest. We estimated the current population growth rate, λ _H , to be 1.025 ± 0.032. Although this suggests the population is growing, progressive environmental changes may require more frequent population inventory studies to maintain the same levels of harvest risk.