scholarly journals Do Wild Polar Bears (Ursus maritimus) Use Tools When Hunting Walruses (Odobenus rosmarus)?

ARCTIC ◽  
2021 ◽  
Vol 74 (2) ◽  
pp. 175-187
Author(s):  
Ian Stirling ◽  
Kristin L. Laidre ◽  
Erik W. Born

Since the late 1700s, reports of polar bears (Ursus maritimus) using tools (i.e., pieces of ice or stones) to kill walruses (Odobenus rosmarus) have been passed on verbally to explorers and naturalists by their Inuit guides, based on local traditional ecological knowledge (TEK) as well as accounts of direct observations or interpretations of tracks in the snow made by the Inuit hunters who reported them. To assess the possibility that polar bears may occasionally use tools to hunt walruses in the wild, we summarize 1) observations described to early explorers and naturalists by Inuit hunters about polar bears using tools, 2) more recent documentation in the literature from Inuit hunters and scientists, and 3) recent observations of a polar bear in a zoo spontaneously using tools to access a novel food source. These observations and previously published experiments on brown bears (Ursus arctos) confirm that, in captivity, polar and brown bears are both capable of conceptualizing the use of a tool to obtain a food source that would otherwise not be accessible. Based on the information from all our sources, this may occasionally also have been the case in the wild. We suggest that possible tool use by polar bears in the wild is infrequent and mainly limited to hunting walruses because of their large size, difficulty to kill, and their possession of potentially lethal weapons for both their own defense and the direct attack of a predator. 

Zoo Biology ◽  
2021 ◽  
Author(s):  
Charles T. Robbins ◽  
Troy N. Tollefson ◽  
Karyn D. Rode ◽  
Joy A. Erlenbach ◽  
Amanda J. Ardente

1997 ◽  
Vol 8 (2) ◽  
pp. 115-116
Author(s):  
Xu Li ◽  
Li Li ◽  
Yang Xiujuan

Polar Biology ◽  
2020 ◽  
Vol 43 (5) ◽  
pp. 457-465
Author(s):  
Andrew F. Barnas ◽  
David T. Iles ◽  
Tanner J. Stechmann ◽  
Erin M. Wampole ◽  
David N. Koons ◽  
...  

2017 ◽  
Vol 91 (4) ◽  
pp. 440-446 ◽  
Author(s):  
J. Dupouy-Camet ◽  
P. Bourée ◽  
H. Yera

AbstractIn this review, we identified 63 cases reported since World War II of human trichinellosis linked to the consumption of parasitized polar bear (Ursus maritimus) meat. This low number contrasts to the numerous cases of human trichinellosis related to consumption of the meat of black (U. americanus) or brown bears (U. arctos). The prevalence of Trichinella infection is high in bears, but larval muscular burden is usually lower in polar bears compared to other bear species. Polar bears, therefore, seem to play a limited role in the transmission of trichinellosis to humans, as native residents living in the Arctic traditionally consume well-cooked bear meat, and travellers and foreign hunters have only limited access to this protected species due to the declining polar bear population.


2021 ◽  
Vol 1 (4) ◽  
pp. 63-66
Author(s):  
N. V. Esaulova ◽  
◽  
S. V. Naydenko ◽  
O. G. Rudakova ◽  
◽  
...  

The article provides information on monitoring studies of polar bear helminthiasis in the wild population of Franz Josef Land and in zoos in Russia. Wild bears were found to be free from invasion. Analysis of fecal samples from polar bears from 17 zoos showed that the total extensiveness of the invasion was 21%, 2 types of helminths were identified: Baylisascaris transfuga and Diphyllobothrium sp. Samples with helminth eggs were found in zoos in Nizhny Novgorod, Rostov-on-Don, Penza, Udmurtia, Khabarovsk, Novosibirsk, Kazan, Krasnoyarsk, Moscow, Volokolamsk, Seversk, Perm.


1991 ◽  
Vol 69 (12) ◽  
pp. 2985-2992 ◽  
Author(s):  
Matthew A. Cronin ◽  
Steven C. Amstrup ◽  
Gerald W. Garner ◽  
Ernest R. Vyse

We assessed mitochondrial DNA variation in North American black bears (Ursus americanus), brown bears (Ursus arctos), and polar bears (Ursus maritimus). Divergent mitochondrial DNA haplotypes (0.05 base substitutions per nucleotide) were identified in populations of black bears from Montana and Oregon. In contrast, very similar haplotypes occur in black bears across North America. This discordance of haplotype phylogeny and geographic distribution indicates that there has been maintenance of polymorphism and considerable gene flow throughout the history of the species. Intraspecific mitochondrial DNA sequence divergence in brown bears and polar bears is lower than in black bears. The two morphological forms of U. arctos, grizzly and coastal brown bears, are not in distinct mtDNA lineages. Interspecific comparisons indicate that brown bears and polar bears share similar mitochondrial DNA (0.023 base substitutions per nucleotide) which is quite divergent (0.078 base substitutions per nucleotide) from that of black bears. High mitochondrial DNA divergence within black bears and paraphyletic relationships of brown and polar bear mitochondrial DNA indicate that intraspecific variation across species' ranges should be considered in phylogenetic analyses of mitochondrial DNA.


2007 ◽  
Vol 52 (4) ◽  
Author(s):  
J. Dubey ◽  
Benjamin Rosenthal ◽  
Natarajan Sundar ◽  
G. Velmurugan ◽  
Kimberlee Beckmen

AbstractThe tissues of herbivores are commonly infected with cysts of parasites belonging to the apicomplexan genus Sarcocystis, but such sarcocysts are rare in bears. Here, we describe a new species, Sarcocystis arctosi, based on the mature sarcocysts identified in two brown bears (Ursus arctos) from Alaska, USA. Microscopic sarcocysts (37–75 × 20–42 μm) had thin walls (<1 μm). The outer layer of the sarcocyst, the parasitophorous vacuolar membrane (pvm), was wavy in outline and had minute undulations that did not invaginate towards the sarcocyst interior; these undulations occurred at irregular intervals and measured up to 100 nm in length and up to 60 nm width. The ground substance layer beneath the pvm was smooth and lacked microtubules. Longitudinally cut bradyzoites measured 5.6–6.8 × 0.7–1.8 μm. A major portion of nuclear small subunit rDNA sequence obtained from these sarcocysts was similar to that previously obtained from the hepatic schizonts of a S. canis-like parasite from polar bears (Ursus maritimus).


2014 ◽  
Vol 105 (3) ◽  
pp. 312-323 ◽  
Author(s):  
Matthew A. Cronin ◽  
Gonzalo Rincon ◽  
Robert W. Meredith ◽  
Michael D. MacNeil ◽  
Alma Islas-Trejo ◽  
...  

2021 ◽  
Author(s):  
Tianying Lan ◽  
Kalle Leppala ◽  
Crystal Tomlin ◽  
Sandra L Talbot ◽  
George K Sage ◽  
...  

The polar bear (Ursus maritimus) has become a symbol of the threat to biodiversity from climate change. Understanding polar bear evolutionary history may provide insights into apex carnivore responses and prospects during periods of extreme environmental perturbations. In recent years, genomic studies have examined bear speciation and population history, including evidence for ancient admixture between polar bears and brown bears (Ursus arctos). Here, we extend our earlier studies of a 130,000-115,000-year-old polar bear from the Svalbard Archipelago using 10X coverage genome sequence and ten new genomes of polar and brown bears from contemporary zones of overlap in northern Alaska. We demonstrate a dramatic decline in effective population size for this ancient polar bear's lineage, followed by a modest increase just before its demise. A slightly higher genetic diversity in the ancient polar bear suggests a severe genetic erosion over a prolonged bottleneck in modern polar bears. Statistical fitting of data to alternative admixture graph scenarios favors at least one ancient introgression event from brown bears into the ancestor of polar bears, possibly dating back over 150,000 years. Gene flow was likely bidirectional, but allelic transfer from brown into polar bear is the strongest detected signal, which contrasts with other published works. These findings have implications for our understanding of climate change impacts: polar bears, a specialist Arctic lineage, may not only have undergone severe genetic bottlenecks, but also been the recipient of generalist, boreal genetic variants from brown bear during critical phases of Northern Hemisphere glacial oscillations.


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