scholarly journals Anatomical and histological studies on the eyes of brown bear (Ursus arctos horribilis)

2020 ◽  
Vol 44 (4) ◽  
pp. 871-878
Author(s):  
Gülseren KIRBAŞ DOĞAN ◽  
Serap KORAL TAŞÇI ◽  
Semine DALGA ◽  
Serap İLHAN AKSU
2018 ◽  
Vol 54 (3) ◽  
pp. 642-645 ◽  
Author(s):  
Susan Knowles ◽  
Barbara L. Bodenstein ◽  
Troy Hamon ◽  
Michael W. Saxton ◽  
Jeffrey S. Hall

2021 ◽  
Vol 39 (2) ◽  
pp. 587-591
Author(s):  
Gülseren Kirbas-Dogan ◽  
Iftar Gürbüz ◽  
Yasin Demiraslan ◽  
Ismet Takci

2007 ◽  
Author(s):  
Sean D. Farley ◽  
Herman Griese ◽  
Rick Sinnott ◽  
Jessica Coltrane ◽  
Chris Garner ◽  
...  

Land ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 146
Author(s):  
Mihai Mustățea ◽  
Ileana Pătru-Stupariu

Human–wildlife interactions (HWI) were frequent in the post-socialist period in the mountain range of Central European countries where forest habitats suffered transitions into built-up areas. Such is the case of the Upper Prahova Valley from Romania. In our study, we hypothesized that the increasing number of HWI after 1990 could be a potential consequence of woodland loss. The goal of our study was to analyse the effects of landscape changes on HWI. The study consists of the next steps: (i) applying 450 questionnaires to local stakeholders (both citizens and tourists) in order to collect data regarding HWI temporal occurrences and potential triggering factors; (ii) investigating the relation between the two variables through the Canonical Correspondence Analysis (CCA); (iii) modelling the landscape spatial changes between 1990 and 2018 for identifying areas with forest loss; (iv) overlapping the distribution of both the households affected by HWI and areas with loss of forested ecosystems. The local stakeholders indicate that the problematic species are the brown bear (Ursus arctos), the wild boar (Sus scrofa), the red fox (Vulpes vulpes) and the grey wolf (Canis lupus). The number of animal–human interactions recorded an upward trend between 1990 and 2018, and the most significant driving factors were the regulation of hunting practices, the loss of habitats, and artificial feeding. The landscape change analysis reveals that between 1990 and 2018, the forest habitats were replaced by built-up areas primarily on the outskirts of settlements, these areas coinciding with frequent HWI. The results are valid for both forest ecosystems conservation in the region, wildlife management, and human infrastructures durable spatial planning.


2017 ◽  
Vol 280 ◽  
pp. S198
Author(s):  
Dubravka Rašić ◽  
Maja Lazarus ◽  
Đuro Huber ◽  
Slaven Reljić ◽  
Maja Peraica
Keyword(s):  

2005 ◽  
Vol 41 (4) ◽  
pp. 825-828 ◽  
Author(s):  
Erik Ågren ◽  
Arne Söderberg ◽  
Torsten Mörner

2017 ◽  
Vol 114 (39) ◽  
pp. 10432-10437 ◽  
Author(s):  
William W. Deacy ◽  
Jonathan B. Armstrong ◽  
William B. Leacock ◽  
Charles T. Robbins ◽  
David D. Gustine ◽  
...  

Climate change is altering the seasonal timing of life cycle events in organisms across the planet, but the magnitude of change often varies among taxa [Thackeray SJ, et al. (2016) Nature 535:241–245]. This can cause the temporal relationships among species to change, altering the strength of interaction. A large body of work has explored what happens when coevolved species shift out of sync, but virtually no studies have documented the effects of climate-induced synchronization, which could remove temporal barriers between species and create novel interactions. We explored how a predator, the Kodiak brown bear (Ursus arctos middendorffi), responded to asymmetric phenological shifts between its primary trophic resources, sockeye salmon (Oncorhynchus nerka) and red elderberry (Sambucus racemosa). In years with anomalously high spring air temperatures, elderberry fruited several weeks earlier and became available during the period when salmon spawned in tributary streams. Bears departed salmon spawning streams, where they typically kill 25–75% of the salmon [Quinn TP, Cunningham CJ, Wirsing AJ (2016) Oecologia 183:415–429], to forage on berries on adjacent hillsides. This prey switching behavior attenuated an iconic predator–prey interaction and likely altered the many ecological functions that result from bears foraging on salmon [Helfield JM, Naiman RJ (2006) Ecosystems 9:167–180]. We document how climate-induced shifts in resource phenology can alter food webs through a mechanism other than trophic mismatch. The current emphasis on singular consumer-resource interactions fails to capture how climate-altered phenologies reschedule resource availability and alter how energy flows through ecosystems.


1976 ◽  
Vol 13 (2) ◽  
pp. 341-347 ◽  
Author(s):  
Charles S. Churcher ◽  
Alan V. Morgan

The distal end of the left humerus of a grizzly bear, Ursus arctos, has been recovered from above the Early Wisconsin Sunnybrook Till at Woodbridge, Ontario, from the same horizon that previously has yielded remains of the woolly mammoth, Mammuthus primigenius. The age of these specimens is estimated at 40 000–50 000 years BP, within the mid-Wisconsin, Port Talbot Interstadial. The only other recognized Canadian record of a grizzly bear east of Manitoba is from a gravel sequence at Barrie, near Lake Simcoe, Ontario, dated from a bone fragment to 11 700 ± 250 years BP. A specimen recovered in Toronto in 1913 from an Early Wisconsin horizon is also considered to represent the grizzly. Bears of the grizzly type, Ursus arctos-horribilis were present in Ontario before and after the Early and Late Wisconsin ice advances.


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