On the mating system of polar bears

1986 ◽  
Vol 64 (10) ◽  
pp. 2142-2151 ◽  
Author(s):  
Malcolm A. Ramsay ◽  
Ian Stirling

Polar bears are intimately associated with arctic sea ice and their distribution is approximated by its winter extent. They are the only terrestrial mammals, other than humans, to have adapted so completely to sea ice, a quite different habitat, spatially and temporally, from that occupied by other terrestrial mammals. We propose that the dynamics of sea ice and the associated variability in access to food have played a major role in the evolution of the social structure and mating system of polar bears. Adult females and males move to areas of the sea ice where the greatest success in hunting is realized. Such regions are unpredictable in location, however, both seasonally and annually. Because female distributions are unpredictable, adult males are unable to defend stable territories that will encompass the home ranges of one or more females and may instead distribute themselves among different sea-ice habitats at the same relative densities as solitary adult females. Females keep nursing cubs with them for more than 1 year; hence the mean interbirth interval is 2 or more years. This results in a functionally skewed sex ratio, with fewer females available to breed in any one year than males, and in intrasexual competition among males for access to breeding females. Consequently, established dominance hierarchies among males are unstable, and wounding, scarring, and breakage of canine teeth are common; these are evidence of direct physical confrontations during the breeding season. Large body size is advantageous in these fights and this has resulted in one of the highest degrees of sexual dimorphism among terrestrial mammals. Because of the funtionally skewed sex ratio and the shifting distribution of both females and males, however, even the largest male probably cannot be certain of locating a larger than average number of receptive females in any one breeding season.

Polar Record ◽  
1993 ◽  
Vol 29 (168) ◽  
pp. 13-24 ◽  
Author(s):  
Ian Stirling ◽  
Dennis Andriashek ◽  
Wendy Calvert

ABSTRACTBetween late March and May, from 1971 through 1979, we surveyed 74,332 km2 of sea-ice habitatin the eastern Beaufort Sea and Amundsen Gulf in the western Canadian Arctic. We defined seven sea-ice habitat types and recorded sightings of polar bears and their tracks in each to determine their habitat preferences. 791 bears (including cubs) and 6454 sets of tracks were recorded. 42.3%, 39.7%, and 15.6% of the bears were seen on floe-edge, moving ice, and drifted fast-ice habitats, respectively. Significant differences in habitat preferences were shown by bears of different sexes and age classes. Adult females accompanied by cubs of the year were the only group that showed a strong preference for fast ice with drifts, probably because they could feed adequately there while avoiding adult males that might prey upon their cubs. The highest densities of seals are found in floe-edge and moving ice habitats and this likely explains the predominance of bears there. Lone adult females and females with two-year-old cubs, adult males, and subadult males were found two and one-half to four times more frequently than predicted in floe-edge habitat. Since there are no data to suggest seals are more abundant along the floe edge than in moving ice habitat, the preference of these groups of adult polar bears for the floe edge in spring may be related to reproductive behavior.


2021 ◽  
Author(s):  
David Lipson ◽  
Kim Reasor ◽  
Kååre Sikuaq Erickson

<p>In this project we analyze artwork and recorded statements of 5<sup>th</sup> grade students from the community of Utqiaġvik, Alaska, who participated in a science-art outreach activity. The team consisted of a scientist (Lipson), an artist (Reasor) and an outreach specialist (Erickson) of Inupiat heritage from a village in Alaska. We worked with four 5th grade classes of about 25 students each at Fred Ipalook Elementary. The predominantly Inupiat people of Utqiaġvik are among those who will be most impacted by climate change and the loss of Arctic sea ice in the near future. Subsistence hunting of marine mammals associated with sea ice is central to the Inupiat way of life. Furthermore, their coastal homes and infrastructure are increasingly subject to damage from increased wave action on ice-free Beaufort and Chukchi Seas. While the people of this region are among the most directly vulnerable to climate change, the teachers reported that the subject is not generally covered in the elementary school curriculum.</p><p>The scientist and the local outreach specialist gave a short presentation about sea ice and climate change in the Arctic, with emphasis on local impacts to hunting and infrastructure. We then showed the students a large poster of historical and projected sea ice decline, and asked the students to help us fill in the white space beneath the lines. The artist led the children in making small paintings that represent things that are important to their lives in Utqiaġvik (they were encouraged to paint animals, but they were free to do whatever they wanted). We returned to the class later that week and had each student briefly introduce themselves and their painting, and place it on the large graph of sea ice decline, which included the dire predictions of the RCP8.5 scenario. Then we added the more hopeful RCP2.6 scenario to end on a positive note.</p><p>Common themes expressed in the students’ artwork included subsistence hunting, other aspects of traditional Inupiat culture, nature and family. Modern themes such as sports and Pokémon were also common. The students reacted to the topic of climate change with pictures of whales, polar bears and other animals, and captions such as “Save the world/ice/animals.” There were several paintings showing unsuccessful hunts for whales or seals. Some students displayed an understanding of ecosystem science in their recorded statements. For example, a student who painted the sun and another who painted a krill both succinctly described energy flow in food webs that support the production of whales (for example, “I drew krill because without krill there wouldn’t be whales”). Some of the students described the consequences of sea ice loss to local wildlife with devastating succinctness (sea ice is disappearing and polar bears will go extinct). The overall sense was that the children had a strong grasp of the potential consequences of climate change to their region and way of life.</p>


2016 ◽  
Vol 12 (12) ◽  
pp. 20160556 ◽  
Author(s):  
Eric V. Regehr ◽  
Kristin L. Laidre ◽  
H. Resit Akçakaya ◽  
Steven C. Amstrup ◽  
Todd C. Atwood ◽  
...  

Loss of Arctic sea ice owing to climate change is the primary threat to polar bears throughout their range. We evaluated the potential response of polar bears to sea-ice declines by (i) calculating generation length (GL) for the species, which determines the timeframe for conservation assessments; (ii) developing a standardized sea-ice metric representing important habitat; and (iii) using statistical models and computer simulation to project changes in the global population under three approaches relating polar bear abundance to sea ice. Mean GL was 11.5 years. Ice-covered days declined in all subpopulation areas during 1979–2014 (median −1.26 days year −1 ). The estimated probabilities that reductions in the mean global population size of polar bears will be greater than 30%, 50% and 80% over three generations (35–41 years) were 0.71 (range 0.20–0.95), 0.07 (range 0–0.35) and less than 0.01 (range 0–0.02), respectively. According to IUCN Red List reduction thresholds, which provide a common measure of extinction risk across taxa, these results are consistent with listing the species as vulnerable. Our findings support the potential for large declines in polar bear numbers owing to sea-ice loss, and highlight near-term uncertainty in statistical projections as well as the sensitivity of projections to different plausible assumptions.


1971 ◽  
Vol 19 (3) ◽  
pp. 267 ◽  
Author(s):  
I Stirling

A. forsteri pups were all weaned by 1 year old and were then totally absent from the island during the breeding season. The recorded intervals, for three tagged females, between apparent weaning of one pup and birth of the next were 29, 40, and 60 days. Some females became infested with barnacles during the period of feeding at sea prior to parturition. Adult females showed a high degree of fidelity to specific breeding colonies. Little specific behaviour, other than restlessness, preceded birth. Five observed births took from 5 sec to 4 min. Pups could swim when born. Male and female newborn pups weighed 4.41 =0.60 and 4.11 +O.47 kg respectively; the sex ratio was not significantly different from unity. Pups stayed with their mothers at a specific location for the first few days, after which the females began to feed at sea and the pups began to associate with each other. Females had not established regular patterns of presence and absence in the pupping colony by early February, but did so by late April. Females did not defend even newborn pups from approaching humans.


1990 ◽  
Vol 68 (1) ◽  
pp. 121-127 ◽  
Author(s):  
Johan Elmberg

A population of individually marked adult Rana temporaria was studied during the breeding season in 1979–1988 in east-central Sweden. Annual return rate averaged 31% (range 16–51%) in males and 16% (range 5–33%) in females. Return rate was not size dependent but increased with every successful previous hibernation, indicating an increased survival rate with age. Return rate was not correlated with winter harshness. Once adult, males had on average 1.5 (maximum 6) seasons with the possibility of reproducing. Corresponding values for females were 1.4 and 4. Mean length of the breeding season was 20 (SD = 2) days. Calling generally started at water temperatures below 3 °C. The lowest spawning temperature was 1 °C. Average temperatures at spawning onset and peak spawning were 5 and 6 °C, respectively. Large males tended to arrive earlier at the pond than small males. Males arrived earlier and stayed longer than did females. The overall population sex ratio was close to unity. The operational sex ratio (OSR) varied during the breeding season, averaging 0.54 (one female to two males). No male was observed to mate more than once per season. I argue that survival selection is more important to male lifetime mating success than is competition in the breeding pond (sexual selection as affected by OSR and length of the breeding season).


2003 ◽  
Vol 51 (4) ◽  
pp. 367 ◽  
Author(s):  
Kylie A. Robert ◽  
Michael B. Thompson ◽  
Frank Seebacher

Females of the Australian scincid lizard Eulamprus tympanum can manipulate the sex of their offspring in response to gender imbalances in the population using temperature-dependent sex determination. Here we show that when adult males are scarce females produced male-biased litters and when adult males were common females produced female-biased litters. The cues used by a female to assess the adult population are not known but presumably depend upon her experience throughout the breeding season. Maternal manipulation of the sex ratio of the offspring in E. tympanum illustrates a selective advantage of temperature-dependent sex determination in a viviparous species.


2021 ◽  
Vol 50 (10) ◽  
pp. 2877-2884
Author(s):  
Zahid Farooq ◽  
Irfan Baboo ◽  
Muhammad Younas ◽  
Khalid Javed Iqbal ◽  
Sana Asad ◽  
...  

Management practices/strategies to re-modulate the wild behaviour of animal species could increase their number in natural areas. The captive herd of hog deer showed slight changes from wild behaviour due to captive stress with no alteration in wild behaviour pattern except captive stress. Adult males (6), adult females (6) and fawns (6) were selected and observed round the clock for thirty days across season after one-hour interval on each activity. All subjects in hotter part of the day spent more time in sitting and rest. While, few hours of night in sleeping, resting and rumination. Fawn spent more time in sitting, resting, and hiding compared to adults. During wandering, they also spent some time in standing. It was noticed that all hog deer in herd not slept together but few of them remain active. Only male fighting was observed and maximum was noticed in August and September during breeding season. Hog deer were mainly crepuscular in feeding with irregular short intakes, and grazing on grasses present in enclosure. This study provides guideline to rehabilitate wild hog deer for better breeding management, conservation and raising practices.


2019 ◽  
Vol 109 ◽  
Author(s):  
Jersei N. Silva ◽  
Guilherme de Oliveira ◽  
Sérgio S. da Rocha

ABSTRACT We analyzed the microhabitat preferences of Macrobrachium jelskii (Miers, 1877) males and females inhabiting an urban water reservoir in Cruz das Almas, Bahia, Brazil. Prawns were collected monthly, from March 2015 to February 2016, in three microhabitats, using a sieve. Each microhabitat was dominated by one macrophyte species: Eleocharis sp. (M1), Cabomba sp. (M2), and Nymphaea sp. (M3). The prawns were measured (carapace length), and categorized as juvenile males, adult males, juvenile females, non-ovigerous adult females and ovigerous adult females. An analysis of variance (ANOVA) was used to compare the number and size of individuals. The sex ratio and frequency of ovigerous females in the three microhabitats were also calculated. The sex ratio was biased towards females in M1 and did not deviate from 1:1 in M2 and M3. When prawns were separated into five categories we observed that non-ovigerous adult females were more abundant in M1, while adult males were the most abundant demographic category in M2 and M3. Juveniles of both sexes and ovigerous females showed no microhabitat preference, although M1 and M2 appeared to be more suitable for the latter. Adult females were the largest individuals in all microhabitats. Food availability, lower depth and lower predation pressure in M1 are the main factors that make M1 more suitable for M. jelskii, particularly non-ovigerous adult females and larger adult males. Intraspecific competition for shelter in M1 might also occur and adult females win this competition due to their larger body size. Therefore, adult males are found in higher abundance in M2 and M3 and the juvenile of both sexes spread evenly across all microhabitats. Our results help to understand the ecological role and the niche used by M. jelskii. Future studies on the habitat choice and predation under laboratory conditions should help to understand the behavior of this species.


2021 ◽  
Vol 13 (9) ◽  
pp. 19232-19238
Author(s):  
Mujahid Ahamad ◽  
Jamal A. Khan ◽  
Satish Kumar

Information on the status of the Indian Blackbuck Antilope cervicapra is mostly available from protected areas (PA), although 80% of its population occurs outside PAs. We conducted surveys to assess the status, age structure, sex ratio, and conservation issues of Blackbuck in and around Aligarh between February and June 2014. A median of 672 individuals at 18 separate locations were recorded with a group size ranging 4–216 except for solitary individuals. The abundance of Blackbuck was maximum in Sikandra Rao (range: 154–216) followed by Andla (range: 47–65), and Pala-Sallu (range: 53–62). Sex ratio was skewed towards females (1:4.5) with yearling to female and fawn to female ratio of 7.8:100 and 6.7:100, respectively. The percentage of adult males of Blackbuck (12.8% adult males, 8.4% sub-adult males) as well as adult females (56.4% adult females, 11.9% sub-adult females) was higher than other age classes or groups in the population. The preliminary observations indicate that the increasing population of free-ranging feral dogs, degradation of forest patches, social forestry plantations, competition with livestock, and poaching pressure are the major conservation issues of Blackbuck in the area. The current information is expected to serve as baseline in assessing the population of Blackbuck in the future. 


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